disease_id,name,synonyms,doid,omim,orphanet,umls,doc2vec_embedding,ncit,efo,mesh,icd9,icd10cm,meddra,hp
mondo:0054615,spermatogenic failure 18,"['spermatogenic failure 18', 'SPGF18']",0070165,617576,,,,,,,,,,
mondo:0054636,Skraban-Deardorff syndrome,"['Skraban-Deardorff syndrome', 'intellectual disability with seizures, abnormal Gait, and distinctive Facial features', 'SKDEAS']",,617616,513456,C4539927,"['0.001599', '0.005844', '-0.009766', '-0.00683', '-0.00456', '-0.00647', '0.000627', '0.001681', '-0.00876', '-0.002878', '0.00833', '-0.006016', '0.001319', '0.004963', '-0.001393', '-0.01027', '0.002293', '-0.006695', '0.00545', '-0.006638', '0.00592', '-0.0009274', '0.012665', '0.00524', '0.002193', '-0.003023', '-0.00813', '-0.008156', '-0.001047', '0.0002441', '0.002398', '-0.0102', '0.00574', '-0.001675', '0.00743', '-0.002348', '0.009544', '-0.0008826', '-0.0003293', '-0.000853', '0.006718', '0.004456', '0.0081', '-0.006905', '-0.00585', '-0.003576', '-0.008385', '0.0002254', '-0.005733', '-0.006126', '-0.003807', '-0.005936', '0.002748', '-0.00309', '-0.00853', '0.003195', '0.003328', '-0.009186', '-0.004063', '-0.004257', '-0.002954', '0.001728', '0.00651', '-0.004116', '-0.001345', '-0.005253', '0.01106', '0.00933', '-0.01339', '0.00658', '-0.01058', '0.008125', '0.00689', '-0.0091', '0.00249', '0.001329', '0.001615', '-0.005066', '0.006683', '-0.002798', '0.006424', '0.005093', '0.006794', '0.01357', '-0.006325', '0.00124', '0.00804', '0.01057', '-0.003708', '-0.00123', '0.004135', '0.002335', '-0.004276', '0.00377', '0.01211', '0.001946', '-0.004208', '-0.002903', '0.00604', '0.005344']",,,,,,,
mondo:0054637,Noonan syndrome-like disorder with loose anagen hair 1,"['NSLH1', 'Tosti syndrome', 'Noonan syndrome-like disorder with loose anagen hair 1', 'Noonan syndrome-like with loose anagen hair 1', 'NSLH']",0080692,607721,,,,C176939,,,,,,
mondo:0054654,combined oxidative phosphorylation deficiency 32,"['COXPD32', 'combined oxidative phosphorylation deficiency 32']",0111492,617664,,C4540029,,,,,,,,
mondo:0054665,"pituitary adenoma 3, multiple types","['PITA3', 'pituitary adenoma 3, multiple types, somatic', 'pituitary adenoma 3, multiple types']",0112010,617686,,C4540135,,,,,,,,
mondo:0054666,ovarian dysgenesis 5,"['ovarian dysgenesis 5', 'ODG5']",0080497,617690,,C4540141,,,,,,,,
mondo:0054669,"pontocerebellar hypoplasia, type 11","['Pontocerebellar hypoplasia due to TBC1D23', 'PCH11', 'pontocerebellar hypoplasia, type 11']",0112324,617695,611247,,,,,,,,,
mondo:0054677,combined oxidative phosphorylation deficiency 33,"['combined oxidative phosphorylation deficiency 33', 'COXPD33']",0111495,617713,,C4540209,"['-0.299', '0.2695', '-0.109', '0.03467', '0.1617', '-0.202', '-0.05118', '0.12134', '-0.2815', '-0.1724', '0.03586', '0.01222', '0.1566', '-0.1749', '0.1235', '-0.1173', '-0.07245', '-0.134', '-0.242', '-0.3228', '0.0924', '-0.2235', '0.3665', '0.04117', '0.1255', '0.0877', '0.04572', '0.0932', '-0.01294', '-0.1675', '0.2012', '0.2329', '0.335', '0.0602', '-0.1084', '-0.2642', '0.0386', '-0.1201', '-0.0761', '-0.2098', '0.1401', '-0.3242', '0.01225', '0.04764', '-0.2395', '-0.317', '0.0796', '-0.02252', '0.2428', '0.0734', '-0.10315', '-0.2632', '-0.05484', '-0.0984', '-0.135', '-0.2048', '0.3523', '-0.0426', '-0.0682', '0.1159', '0.1787', '0.11084', '0.3792', '-0.101', '0.1426', '0.1549', '0.1807', '0.1282', '-0.2896', '0.227', '-0.2393', '-0.09863', '0.0379', '0.017', '0.2024', '0.1978', '0.1351', '0.0931', '-0.05905', '0.0787', '0.1182', '0.02618', '-0.04114', '0.1531', '0.00221', '0.00664', '0.1531', '0.257', '0.3037', '0.1786', '0.1715', '0.1514', '-0.03348', '-0.1864', '0.606', '0.2961', '0.2072', '-0.4321', '-0.01651', '0.05215']",C174440,0009159,,,,,
mondo:0054680,"epiphyseal dysplasia, multiple, 7","['epiphyseal dysplasia, multiple, 7', 'EDM7', 'multiple epiphyseal dysplasia 7', 'multiple epiphyseal dysplasia type 7']",0070302,617719,647676,,,,,,,,,
mondo:0054691,"immunodeficiency, common variable, 14","['immunodeficiency, COMMON variable, 14', 'CVID14']",0081156,617765,,C4540380,,,,,,,,
mondo:0054695,"myopathy, centronuclear, 6, with fiber-type disproportion","['myopathy, centronuclear, 6, with FIBER-type disproportion', 'CNM6', 'centronuclear myopathy 6 with fiber-type disproportion']",0111221,617760,,C4540345,"['-0.0809', '0.09064', '-0.0226', '-0.01631', '0.04648', '-0.1731', '0.02444', '0.145', '-0.1246', '-0.0641', '-0.0292', '0.02036', '-0.002848', '0.00245', '-0.0263', '-0.02222', '-0.000818', '-0.04578', '-0.04816', '-0.1926', '-0.005814', '-0.02367', '0.09283', '0.00569', '0.02682', '-0.03433', '-0.02846', '-0.05997', '-0.01334', '-0.08136', '0.0784', '0.005337', '0.0766', '0.03714', '0.01747', '-0.04767', '-0.0484', '-0.0776', '-0.00591', '-0.0564', '-0.0318', '-0.12164', '0.03812', '0.00451', '-0.006027', '-0.0672', '-0.05164', '0.0843', '-0.01461', '0.01561', '-0.0719', '-0.00858', '-0.002424', '-0.01993', '-0.02759', '-0.0481', '0.1216', '-0.05527', '-0.1098', '-0.00204', '0.0907', '0.02962', '0.0076', '0.03114', '-0.01105', '0.00567', '0.1218', '0.1053', '-0.1342', '0.1146', '-0.0878', '-0.01347', '0.03677', '-0.0653', '0.08307', '0.04517', '0.00535', '-0.042', '-0.06384', '-0.0747', '0.03055', '-0.004414', '-0.01145', '0.1223', '0.01839', '0.0492', '-0.0083', '0.1454', '0.1065', '-0.01187', '0.0685', '0.0541', '0.01467', '0.03897', '0.2026', '0.04422', '0.1201', '-0.1105', '-0.01697', '-0.01959']",,,,,,,
mondo:0054696,immunodeficiency 53,"['IMD53', 'immunodeficiency 53']",0111992,617585,,C4539811,,,,,,,,
mondo:0054697,immunodeficiency 11b with atopic dermatitis,"['immunodeficiency 11B with ATOPIC dermatitis', 'atopic dermatitis, elevated IgE, and eosinophilia', 'IMD11B']",0111958,617638,,C4539957,,C176630,,,,,,
mondo:0054698,proteasome-associated autoinflammatory syndrome 1,"['chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome', 'PRAAS1', 'autoinflammation, lipodystrophy, and dermatosis syndrome', 'proteasome-associated autoinflammatory syndrome 1, digenic', 'JMP syndrome', 'joint contractures, muscular atrophy, microcytic Anemia, and panniculitis-induced lipodystrophy', 'Nakajo-Nishimura syndrome', 'proteasome-associated autoinflammatory syndrome 1 and digenic forms', 'proteasome-associated autoinflammatory syndrome 1']",,256040,,,,C176619,,,,,,
mondo:0054699,proteasome-associated autoinflammatory syndrome 3,"['proteasome-associated autoinflammatory syndrome 3, digenic', 'proteasome-associated autoinflammatory syndrome 3', 'proteasome-associated autoinflammatory syndrome 3 and digenic forms', 'PRAAS3']",,617591,,,"['-0.01822', '0.0962', '-0.02617', '-0.02843', '0.0354', '-0.11694', '-0.005276', '0.0918', '-0.0771', '-0.04773', '-0.03497', '0.03146', '0.006752', '-0.01881', '-0.0332', '-0.035', '0.001866', '-0.03336', '0.003027', '-0.1335', '-0.01595', '-0.03035', '0.0955', '-0.0583', '0.00896', '0.01663', '-0.03192', '-0.03125', '-0.003458', '-0.05475', '0.06555', '0.0008135', '0.09534', '0.0563', '-0.01521', '-0.03085', '-0.0148', '-0.04694', '-0.02771', '-0.04803', '0.0435', '-0.12317', '0.03683', '-0.05142', '0.01913', '-0.05722', '-0.06223', '0.04483', '0.0322', '0.0236', '-0.03763', '-0.03613', '0.04376', '0.03069', '-0.0444', '-0.04865', '0.07275', '-0.04578', '-0.1235', '-0.01996', '0.09326', '0.05743', '0.02524', '-0.002655', '0.0315', '-0.006336', '0.1122', '0.05487', '-0.07916', '0.0793', '-0.07764', '0.003803', '0.000824', '-0.03973', '0.03635', '0.04996', '0.0148', '0.02505', '-0.05286', '-0.04117', '0.01093', '0.001785', '-0.04175', '0.0712', '-0.01628', '0.00638', '0.0706', '0.155', '0.0843', '0.03204', '0.04578', '0.0697', '0.02423', '0.01432', '0.1464', '0.04156', '0.1077', '-0.1267', '-0.01909', '0.002542']",,,,,,,
mondo:0054700,proteasome-associated autoinflammatory syndrome 2,"['PRAAS2', 'proteasome-associated autoinflammatory syndrome 2']",,618048,,CN252342,"['-0.00846', '0.05057', '0.00367', '-0.02179', '0.0091', '-0.05826', '-0.00362', '0.05966', '-0.03464', '-0.019', '-0.02856', '0.00437', '0.01002', '-0.004654', '-0.01817', '-0.02348', '-0.00905', '0.004932', '-0.001834', '-0.08514', '-0.010376', '-0.02321', '0.06433', '-0.03973', '0.01388', '0.01156', '-0.02121', '-0.01559', '0.01315', '-0.0396', '0.04138', '-0.0006423', '0.0468', '0.02321', '0.003754', '-0.01624', '-0.01785', '-0.011375', '-0.00969', '-0.04742', '0.01529', '-0.067', '0.01348', '-0.02919', '0.01272', '-0.0569', '-0.04324', '0.0444', '0.01425', '0.01703', '-0.02199', '-0.01927', '0.01895', '0.001497', '-0.0203', '-0.03238', '0.04935', '-0.03748', '-0.0647', '0.006817', '0.056', '0.017', '0.007133', '-0.00523', '0.01422', '0.008705', '0.06204', '0.02997', '-0.0649', '0.07605', '-0.068', '-0.00234', '0.013535', '-0.03009', '0.04745', '0.03912', '-0.005863', '0.02287', '-0.03674', '-0.03732', '0.01683', '0.00877', '-0.03433', '0.04733', '-0.01213', '0.007153', '0.03333', '0.0847', '0.05698', '0.02695', '0.04233', '0.05438', '0.01048', '0.005005', '0.10095', '0.03008', '0.0657', '-0.0893', '-0.03253', '0.01056']",,,,,,,
mondo:0054701,Kleefstra syndrome 2,"['Kleefstra syndrome 2', 'KLEFS2']",0080598,617768,,,,,,,,,,
mondo:0054708,retinitis pigmentosa 80,"['RETINITIS pigmentosa 80', 'RP80']",,617781,,,,,,,,,,
mondo:0054716,"microcephaly 19, primary, autosomal recessive","['primary autosomal recessive microcephaly 19', 'MCPH19', 'microcephaly 19, PRIMARY, autosomal recessive']",0070281,617800,,C4540488,,,,,,,,
mondo:0054722,geleophysic dysplasia 3,"['GPHYSD3', 'GELEOPHYSIC dysplasia 3']",0111727,617809,,,,,,,,,,
mondo:0054723,spermatogenic failure 19,"['SPGF19', 'spermatogenic failure 19']",0070170,617592,,,,,,,,,,
mondo:0054724,spermatogenic failure 20,"['spermatogenic failure 20', 'SPGF20']",0070166,617593,,,,,,,,,,
mondo:0054725,spermatogenic failure 21,"['spermatogenic failure 21', 'SPGF21']",0070163,617644,,C4539991,,,,,,,,
mondo:0054726,spermatogenic failure 22,"['spermatogenic failure 22', 'SPGF22']",0070177,617706,,,,,,,,,,
mondo:0054727,spermatogenic failure 23,"['SPGF23', 'spermatogenic failure 23']",0070181,617707,,C4540185,,,,,,,,
mondo:0054728,spermatogenic failure 24,"['spermatogenic failure 24', 'SPGF24']",0111929,617959,,CN244570,,,,,,,,
mondo:0054729,spermatogenic failure 25,"['spermatogenic failure 25', 'SPGF25']",0111920,617960,,,,,,,,,,
mondo:0054730,spermatogenic failure 26,"['spermatogenic failure 26', 'SPGF26']",0111924,617961,,CN244573,,,,,,,,
mondo:0054731,spermatogenic failure 27,"['SPGF27', 'spermatogenic failure 27']",0111928,617965,,,,,,,,,,
mondo:0054732,spermatogenic failure 28,"['spermatogenic failure 28', 'SPGF28']",0111916,618086,,,"['-0.04028', '0.0641', '0.003061', '-0.0273', '0.00675', '-0.1169', '-0.00926', '0.1021', '-0.04828', '-0.0633', '-0.0116', '0.003149', '-0.0277', '0.0136', '-0.0394', '-0.06177', '0.0121', '-0.04193', '-0.0002385', '-0.1393', '-0.05344', '-0.04044', '0.05075', '-0.0435', '0.06168', '-0.02046', '-0.01903', '-0.0138', '-0.00952', '-0.05518', '0.05618', '0.02316', '0.0972', '0.02312', '0.02422', '-0.05383', '-0.01799', '-0.02635', '-0.04077', '-0.0728', '0.006664', '-0.0582', '0.0341', '-0.02394', '-0.009674', '-0.0626', '-0.02744', '0.03928', '0.001642', '0.03833', '-0.00968', '-0.01651', '0.003162', '-0.00659', '-0.03047', '-0.02852', '0.0936', '-0.0377', '-0.10297', '0.01913', '0.05057', '0.04974', '0.00427', '-0.0003796', '0.01015', '-0.02191', '0.11456', '0.0637', '-0.10315', '0.07227', '-0.03918', '0.001993', '0.02902', '-0.04883', '0.0485', '0.02626', '0.006077', '-0.03204', '-0.04202', '-0.01199', '0.03943', '0.000631', '-0.02484', '0.03928', '0.01209', '0.00811', '0.04803', '0.03998', '0.10187', '0.0004818', '0.02406', '0.04816', '-0.03482', '0.0335', '0.1522', '0.06995', '0.0561', '-0.0796', '-0.0113', '0.001574']",,,,,,,
mondo:0054733,spermatogenic failure 29,"['spermatogenic failure 29', 'SPGF29']",0111930,618091,,,"['-0.02692', '0.04175', '0.00221', '-0.01248', '0.003273', '-0.06207', '0.01357', '0.0526', '-0.04108', '-0.02168', '-0.01814', '-0.0006633', '-0.00391', '0.00725', '-0.02208', '-0.03943', '-0.009605', '-0.012985', '-0.00394', '-0.09314', '-0.00903', '-0.02277', '0.03378', '-0.02953', '0.01576', '-0.02701', '0.001231', '-0.010704', '-0.00916', '-0.03198', '0.0404', '-0.0053', '0.03348', '0.0142', '0.01921', '-0.02068', '-0.008415', '-0.02148', '-0.0298', '-0.03656', '0.01052', '-0.04355', '0.02164', '-0.003471', '-0.002699', '-0.0401', '-0.01466', '0.02751', '0.012505', '0.01557', '-0.007046', '0.001362', '0.010475', '0.000798', '-0.01608', '-0.006866', '0.04855', '-0.02374', '-0.06064', '0.01088', '0.02116', '0.03192', '-0.00932', '0.006332', '0.00912', '-0.01402', '0.04614', '0.03134', '-0.05038', '0.05267', '-0.02844', '0.008354', '0.01994', '-0.03665', '0.0138', '0.0209', '0.007774', '-0.00967', '-0.02805', '-0.00895', '0.00654', '-0.00961', '-0.02284', '0.03053', '0.01014', '0.001327', '0.01991', '0.03244', '0.05975', '0.009636', '0.02345', '0.03995', '-0.01813', '0.02513', '0.08813', '0.04114', '0.03787', '-0.051', '-0.008255', '0.014854']",,,,,,,
mondo:0054736,mosaic variegated aneuploidy syndrome 3,"['MOSAIC variegated aneuploidy syndrome 3', 'MVA3']",0080689,617598,,,,,,,,,,
mondo:0054737,Fraser syndrome 1,"['cryptophthalmos-syndactyly syndrome', 'FRASRS1', 'Fraser syndrome 1', 'Fraser syndrome', 'cryptophthalmos with Other malformations']",0111405,219000,,,,,,,,,,
mondo:0054738,Fraser syndrome 2,"['Fraser syndrome 2', 'FRASRS2']",0111407,617666,,C4540036,,,,,,,,
mondo:0054739,Fraser syndrome 3,"['Fraser syndrome 3', 'FRASRS3']",0111406,617667,,C4540040,,,,,,,,
mondo:0054740,blepharocheilodontic syndrome 1,"['clefting, ectropion, and conical teeth', 'Lagophthalmia with bilateral cleft 51P and palate', 'ectropion, Inferior, with cleft 51P and/Or palate', 'CDH1 blepharo-cheilo-odontic syndrome', 'BCDS1', 'BCD syndrome', 'blepharocheilodontic syndrome 1', 'elschnig syndrome', 'blepharocheilodontic syndrome']",0080345,119580,,,,,,,,,,
mondo:0054741,combined oxidative phosphorylation deficiency 34,"['combined oxidative phosphorylation deficiency 34', 'COXPD34']",0111497,617872,,,"['-0.01356', '0.01875', '0.00694', '0.003891', '-0.001351', '-0.01231', '0.01081', '0.03232', '-0.01415', '-0.004852', '-0.001436', '-0.00662', '0.007027', '-0.004585', '0.005566', '-0.01921', '-0.01049', '-0.02347', '-0.01625', '-0.03842', '0.0001706', '-0.01116', '0.01677', '-0.00845', '0.002771', '-0.00997', '-0.006664', '-0.00875', '-0.01007', '-0.00551', '0.01933', '0.003056', '0.02599', '0.01659', '0.00901', '-0.00736', '-0.001318', '0.001738', '-0.001639', '-0.012825', '0.0143', '-0.03384', '0.013535', '0.00556', '-0.00819', '-0.02177', '0.00544', '0.00582', '0.00997', '0.0059', '0.001584', '-0.011055', '0.004448', '0.007256', '-0.02522', '-0.00613', '0.02151', '-0.0005527', '-0.02048', '0.01139', '0.01464', '0.003586', '0.015526', '-0.00493', '0.00554', '-0.002129', '0.01319', '0.02469', '-0.03014', '0.02434', '-0.007645', '0.001184', '-0.004906', '-0.0213', '0.02106', '0.003714', '0.01064', '0.00332', '-0.01501', '-0.006924', '0.00466', '-0.002533', '-0.006023', '0.01006', '-0.00857', '0.009445', '0.003345', '0.01239', '0.02176', '-0.004192', '0.01967', '0.00579', '0.00575', '0.0002135', '0.0478', '0.01122', '0.01741', '-0.03314', '-0.00603', '0.007645']",,,,,,,
mondo:0054742,combined oxidative phosphorylation deficiency 35,"['COXPD35', 'combined oxidative phosphorylation deficiency 35']",0111464,617873,,CN807948,"['-0.168', '0.111', '0.008514', '0.03625', '0.0837', '-0.1365', '0.02087', '0.10803', '-0.0814', '-0.04208', '-0.009186', '-0.02441', '0.02274', '-0.0454', '0.0786', '-0.0786', '-0.012825', '-0.0721', '-0.0853', '-0.2135', '-0.01752', '-0.1189', '0.11206', '-0.05655', '-0.000848', '-0.03107', '0.02806', '-0.01079', '-0.05936', '-0.1316', '0.0721', '0.1032', '0.1722', '0.04767', '0.00987', '-0.1305', '0.02882', '-0.08057', '-0.0251', '-0.07086', '0.09033', '-0.1445', '0.00906', '0.03806', '-0.11676', '-0.1198', '0.02739', '0.0632', '0.0347', '0.000987', '-0.04715', '-0.10345', '0.03094', '0.03568', '-0.1101', '-0.0214', '0.1299', '-0.014565', '-0.05624', '0.0505', '0.0843', '0.0771', '0.1141', '-0.02138', '0.001155', '0.04034', '0.1309', '0.05627', '-0.1556', '0.1244', '-0.02525', '-0.0006905', '0.02748', '-0.08777', '0.098', '0.0722', '0.0361', '-0.02742', '-0.011116', '0.0236', '-0.01348', '-0.00866', '-0.02902', '0.08813', '0.0206', '-0.04443', '0.08026', '0.10065', '0.1825', '0.02023', '0.1092', '0.0745', '-0.03183', '-0.00566', '0.2817', '0.1294', '0.0816', '-0.159', '0.01154', '0.02232']",,,,,,,
mondo:0054743,polycystic liver disease 3 with or without kidney cysts,"['polycystic liver disease 3 with or without kidney cysts', 'PCLD3']",,617874,,CN818986,"['0.0169', '0.0745', '0.01473', '-0.04642', '0.04663', '-0.0959', '-0.02103', '0.1248', '-0.073', '-0.02892', '-0.05945', '-0.02872', '-0.00839', '0.05005', '-0.0939', '-0.0859', '4.98e-05', '-0.02069', '-0.00786', '-0.1576', '0.0081', '-0.04782', '0.0836', '-0.03397', '0.02571', '-0.05396', '-0.002945', '0.00766', '0.049', '-0.05252', '0.0987', '-0.04648', '0.10876', '0.01863', '0.0199', '-0.06088', '-0.06158', '-0.0613', '-0.01822', '-0.05746', '0.02518', '-0.05756', '0.05527', '-0.01241', '-0.02614', '-0.0883', '-0.02277', '0.06155', '-0.02515', '0.03723', '-0.02263', '0.02286', '0.03494', '-0.001075', '-0.04556', '-0.03772', '0.08496', '-0.0654', '-0.15', '0.006016', '0.09143', '0.0629', '-0.015495', '0.002983', '-0.012436', '-0.0416', '0.0898', '0.10254', '-0.0837', '0.1039', '-0.04352', '-0.002228', '0.0436', '-0.0704', '0.0338', '0.0264', '0.01067', '0.0338', '-0.0693', '-0.06003', '-0.01698', '-0.003454', '-0.01588', '0.04785', '-0.04825', '-0.006805', '0.04355', '0.084', '0.0939', '0.02284', '0.02545', '0.07715', '0.000853', '0.02567', '0.2083', '0.03078', '0.0663', '-0.1021', '-0.02502', '0.05032']",,,,,,,
mondo:0054748,"Fanconi anemia, complementation group S","['FANCS', 'Fanconi anemia, complementation GROUP S']",,617883,,,"['-0.053', '0.1149', '0.00974', '-0.02861', '0.09625', '-0.0977', '-0.03427', '0.08594', '-0.06476', '-0.093', '-0.0281', '0.02197', '0.00834', '0.0414', '-0.03023', '-0.0691', '-0.03876', '-0.0707', '-0.01733', '-0.1565', '0.03625', '-0.04327', '0.136', '0.013435', '0.03903', '-0.04492', '0.01209', '-0.0247', '-0.002563', '-0.02426', '0.02342', '-0.01326', '0.1305', '0.05713', '0.0513', '-0.03293', '-0.06384', '-0.0956', '-0.0594', '-0.1077', '-0.005974', '-0.1321', '0.07263', '-0.02614', '-0.02112', '-0.135', '-0.02164', '0.0875', '0.07874', '0.014336', '-0.009575', '-0.02953', '0.00993', '0.02655', '-0.03125', '-0.0731', '0.06235', '0.03265', '-0.1567', '0.05618', '0.07043', '0.02467', '-0.01359', '-0.00626', '0.04263', '-0.0003798', '0.0825', '0.1122', '-0.08997', '0.0931', '-0.0522', '-0.0454', '-0.0112', '-0.07336', '0.05823', '0.0687', '0.03375', '-0.02443', '-0.05103', '-0.05704', '0.01643', '-0.04623', '-0.02347', '0.03485', '-0.00576', '0.012054', '0.04852', '0.10254', '0.1267', '-0.02698', '0.09656', '0.02795', '0.003092', '-0.06128', '0.1692', '0.1343', '0.0766', '-0.1332', '-0.01492', '0.05673']",,,,,,,
mondo:0054750,"amyotrophic lateral sclerosis, susceptibility to, 24","['ALS24', 'amyotrophic lateral sclerosis, susceptibility to, 24']",,617892,,CN842244,"['-0.03494', '0.03485', '0.0082', '-0.004215', '0.01305', '-0.0754', '0.03003', '0.04874', '-0.0495', '-0.0327', '-0.0002141', '0.01366', '0.001907', '0.00291', '0.0128', '-0.02802', '-0.005', '-0.02489', '0.003475', '-0.0819', '0.00809', '-0.03452', '0.0364', '-0.009285', '0.00397', '-0.02472', '-0.01244', '0.0008454', '-0.0202', '-0.01744', '0.02847', '-0.02425', '0.0526', '0.007336', '0.02895', '-0.01917', '-0.02629', '-0.0138', '-0.004616', '-0.04465', '0.01782', '-0.02612', '0.01778', '-0.03583', '0.02414', '-0.04672', '0.003765', '0.03632', '0.006172', '0.02567', '-0.01932', '-0.0002801', '0.0178', '0.012665', '-0.02638', '-0.02649', '0.02211', '-0.00954', '-0.04523', '0.003872', '0.02983', '0.02122', '0.00745', '0.0234', '0.005768', '0.0236', '0.05804', '0.0446', '-0.0539', '0.0594', '-0.02844', '0.01467', '0.0079', '-0.05197', '0.01355', '0.02953', '-0.009926', '0.00925', '-0.03516', '-0.03488', '-0.00495', '0.006042', '-0.01397', '0.06137', '-0.00877', '-0.004692', '0.003471', '0.0328', '0.05557', '-0.001275', '0.01034', '0.0266', '0.005997', '0.01591', '0.0875', '0.04007', '0.0495', '-0.0546', '0.00958', '-0.000941']",,,,,,,
mondo:0054752,multiple synostoses syndrome 4,"['SYNS4', 'multiple synostoses syndrome 4']",0081320,617898,,CN842246,,,,,,,,
mondo:0054754,"encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 8","['encephalopathy, ACUTE, infection-induced (HERPES-specific), susceptibility to, 8', 'IIAE8', 'Herpes simplex encephalitis, Susceptibility to, 6']",,617900,,CN865669,,,,,,,,
mondo:0054761,"microcephaly 20, primary, autosomal recessive","['microcephaly 20, PRIMARY, autosomal recessive', 'MCPH20']",,617914,,,,,,,,,,
mondo:0054763,neurodegeneration with brain iron accumulation 7,"['neurodegeneration with brain iron accumulation 7', 'NBIA7']",,617916,,CN895590,,,,,,,,
mondo:0054764,neurodegeneration with brain iron accumulation 8,"['NBIA8', 'neurodegeneration with brain iron accumulation 8']",,617917,,CN895591,"['-0.0759', '0.1766', '0.03967', '-0.0265', '0.10754', '-0.09344', '-0.03117', '0.0936', '-0.0833', '0.0181', '-0.1037', '-0.01828', '0.01831', '-0.03772', '-0.01414', '-0.1293', '-0.01528', '-0.0733', '-0.1241', '-0.178', '-0.05035', '-0.1257', '0.0717', '0.00495', '0.01281', '-0.04178', '0.0183', '-0.0536', '-0.1034', '-0.03754', '0.07446', '0.002695', '0.1434', '0.04547', '0.02573', '-0.03156', '-0.0394', '-0.0751', '-0.006416', '-0.0762', '0.0366', '-0.156', '0.04813', '0.023', '-0.00868', '-0.1033', '0.02963', '0.0672', '-0.01836', '-0.01605', '0.02762', '-0.004814', '-0.01206', '0.0638', '-0.01231', '-0.01883', '0.1251', '0.014435', '-0.1428', '0.04205', '0.07684', '0.007633', '0.0429', '-0.03632', '-0.0278', '-0.000794', '0.1205', '0.0654', '-0.1315', '0.09845', '-0.03464', '-0.0002964', '-0.00212', '-0.0796', '0.03928', '0.0713', '0.03058', '0.013695', '-0.08386', '-0.08203', '-0.007206', '-0.0889', '-0.005886', '0.09125', '0.0529', '-0.04645', '0.05936', '0.1201', '0.1511', '-0.02396', '0.07635', '0.11633', '-0.02345', '-0.03008', '0.2095', '0.1185', '0.0765', '-0.0683', '-0.01224', '-0.02975']",,,,,,,
mondo:0054765,"amyloidosis, primary localized cutaneous, 3","['amyloidosis cutis dyschromica', 'amyloidosis, PRIMARY LOCALIZED cutaneous, 3', 'PLCA3']",,617920,,,,,,,,,,
mondo:0054770,orofaciodigital syndrome 18,"['OFD18', 'orofaciodigital syndrome XVIII', 'oral-Facial-digital syndrome, type 18', 'Ofds 18']",,617927,,CN244546,,,,,,,,
mondo:0054771,keratoconus 9,"['keratoconus 9', 'KTCN9']",,617928,,CN244547,,,,,,,,
mondo:0054776,"epilepsy, familial focal, with variable foci 4","['epilepsy, FAMILIAL focal, with variable foci 4', 'FFEVF4']",,617935,,CN244552,,,,,,,,
mondo:0054780,elliptocytosis 3,"['anemia, neonatal hemolytic, fatal or near-fatal', 'elliptocytosis-3', 'EL3', 'anemia, perinatal hemolytic, fatal or near-fatal', 'elliptocytosis 3']",,617948,,,,,,C566678,,,,
mondo:0054781,combined oxidative phosphorylation deficiency 36,"['combined oxidative phosphorylation deficiency 36', 'COXPD36']",0111482,617950,,CN244569,"['-0.167', '0.1067', '0.01935', '0.0448', '0.0437', '-0.1399', '0.013306', '0.08093', '-0.06635', '-0.01253', '-0.01344', '-0.01429', '0.01753', '-0.04572', '0.03058', '-0.07794', '-0.003918', '-0.0968', '-0.0715', '-0.2023', '-0.001378', '-0.10223', '0.1136', '-0.04465', '0.008736', '-0.0218', '0.04797', '0.0004256', '-0.0498', '-0.088', '0.0635', '0.1085', '0.1799', '0.06003', '0.00782', '-0.1239', '0.02205', '-0.0655', '-0.04422', '-0.07635', '0.07434', '-0.1569', '0.00805', '0.04056', '-0.09656', '-0.1038', '0.01517', '0.06665', '0.006813', '0.01049', '-0.0475', '-0.114', '0.03006', '0.0135', '-0.1101', '-0.02914', '0.1395', '-0.0501', '-0.09753', '0.0721', '0.0755', '0.05814', '0.1037', '-0.03078', '0.001909', '0.02365', '0.1378', '0.05136', '-0.1306', '0.1112', '-0.04053', '-0.02216', '0.01727', '-0.0913', '0.092', '0.04883', '0.015396', '-0.04614', '-0.01912', '0.05432', '0.01796', '0.005024', '-0.03047', '0.08624', '0.02951', '-0.03372', '0.06033', '0.1181', '0.1813', '0.01553', '0.1083', '0.07025', '-0.00603', '0.004917', '0.2627', '0.10846', '0.0877', '-0.1455', '0.0214', '0.03098']",,,,,,,
mondo:0054782,"leukodystrophy, hypomyelinating, 15","['leukodystrophy, hypomyelinating, 15', 'HLD15']",0070398,617951,,CN244566,"['-0.01793', '0.04755', '0.003435', '-0.004833', '0.0222', '-0.0355', '-0.00943', '0.0571', '-0.0398', '-0.003141', '-0.0345', '-9.63e-05', '-0.001965', '-0.02176', '-0.007755', '-0.03372', '0.004547', '-0.02853', '-0.02927', '-0.06537', '-0.003515', '-0.013885', '0.01266', '-0.01921', '0.02576', '-0.01608', '-0.001737', '-0.01055', '-0.00803', '-0.010056', '0.03244', '-0.00965', '0.05444', '0.00822', '0.01796', '-0.03363', '-0.01947', '-0.01802', '-0.01326', '-0.04413', '0.02489', '-0.05328', '0.006428', '-0.01409', '-0.01697', '-0.04993', '-0.001208', '0.01909', '0.00882', '0.00908', '0.0036', '-0.006386', '-0.01949', '-0.00277', '-0.0204', '-0.00853', '0.05914', '-0.02138', '-0.05823', '0.02069', '0.01354', '0.0277', '0.01562', '0.02158', '-0.02354', '0.002764', '0.04892', '0.0334', '-0.05255', '0.0327', '-0.02263', '0.011284', '0.01001', '-0.031', '0.02856', '0.02426', '0.02126', '0.004356', '-0.03113', '-0.0319', '-0.000775', '-0.018', '-0.0162', '0.048', '0.001268', '-0.006256', '0.02092', '0.04706', '0.02705', '0.01415', '0.02815', '0.0259', '0.00191', '0.02217', '0.09424', '0.00572', '0.0419', '-0.05447', '0.0001959', '0.0183']",,,,,,,
mondo:0054785,multiple mitochondrial dysfunctions syndrome 6,"['multiple mitochondrial dysfunctions syndrome type 6', 'multiple mitochondrial dysfunctions syndrome 6', 'PMPCB deficiency', 'MMDS6']",0070332,617954,569290,CN244567,"['-0.0688', '0.11676', '0.00961', '0.044', '0.04083', '-0.1332', '0.0181', '0.1119', '-0.10156', '-0.058', '-0.01817', '0.01947', '0.0308', '-0.0222', '-0.008224', '-0.0802', '-0.02669', '-0.02579', '-0.0266', '-0.1576', '-0.00966', '-0.0571', '0.10986', '-0.05917', '0.04974', '-0.02812', '-0.05725', '-0.01974', '0.006367', '-0.05017', '0.1015', '0.04242', '0.1482', '0.0502', '0.01018', '-0.0864', '-0.02538', '-0.02658', '-0.04785', '-0.07245', '0.05695', '-0.147', '0.03738', '-0.04767', '0.004807', '-0.1349', '-0.06213', '0.0885', '0.00822', '0.00323', '-0.0809', '-0.0327', '-0.00916', '-0.02606', '-0.06415', '-0.06885', '0.10065', '-0.0113', '-0.10095', '0.0441', '0.086', '0.03085', '0.0523', '0.02737', '-0.02928', '0.01819', '0.1472', '0.11005', '-0.1154', '0.1164', '-0.05844', '0.02846', '0.01509', '-0.04926', '0.03705', '0.0539', '-0.01904', '0.03333', '-0.08545', '-0.04678', '0.03023', '0.02505', '-0.0645', '0.08777', '-0.001079', '0.000952', '0.06384', '0.12115', '0.10925', '0.01958', '0.0672', '0.0608', '0.0315', '-0.00515', '0.1986', '0.07056', '0.0937', '-0.1492', '-0.015175', '0.02444']",,,,,,,
mondo:0054791,"leukodystrophy, hypomyelinating, 16","['HLD16', 'leukodystrophy, hypomyelinating, 16']",0070405,617964,,CN244907,,,,,,,,
mondo:0054794,"hydrocephalus, congenital, 3, with brain anomalies","['hydrocephalus, CONGENITAL, 3, with brain anomalies', 'HYC3', 'hydrocephalus, nonsyndromic, autosomal recessive 3', 'hydrocephalus, nonsyndromic, autosomal recessive 3, formerly']",,617967,,,"['-0.02942', '0.113', '0.06052', '-0.05347', '0.07904', '-0.12305', '0.0461', '0.1647', '-0.1624', '-0.0782', '-0.07', '-0.05228', '-0.02322', '0.00827', '-0.0642', '-0.08356', '-0.004646', '-0.1194', '-0.1207', '-0.2479', '0.02008', '-0.01395', '0.1132', '-0.0536', '0.069', '-0.067', '-0.05295', '0.0204', '0.02002', '-0.0503', '0.0978', '-0.04828', '0.2023', '0.08014', '0.02548', '-0.02045', '-0.0006504', '-0.05038', '-0.01721', '-0.1099', '0.07947', '-0.1382', '0.03354', '-0.02554', '0.02081', '-0.0953', '-0.01156', '0.1024', '-0.01613', '0.00956', '-0.02951', '0.004883', '-0.004005', '-0.03522', '-0.077', '0.00584', '0.0648', '-0.02336', '-0.1508', '0.003723', '0.0576', '0.1052', '-0.011566', '0.03894', '-0.06186', '0.006546', '0.1497', '0.1301', '-0.1631', '0.11005', '-0.1134', '0.1021', '0.0487', '-0.1146', '0.01645', '0.04974', '0.04224', '-0.0443', '-0.07513', '-0.104', '-0.0134', '-0.04257', '-0.01569', '0.1909', '-0.04926', '0.000974', '0.0919', '0.1755', '0.1445', '0.001639', '0.02939', '0.1852', '0.0766', '0.03757', '0.2069', '0.0675', '0.145', '-0.1171', '0.0727', '0.0642']",,,,,,,
mondo:0054801,"erythrocytosis, familial, 6","['erythrocytosis, Beta-globin type', 'polycythemia, Beta-globin type', 'erythrocytosis, FAMILIAL, 6', 'ECYT6', 'erythrocytosis 6']",0111632,617980,,CN244941,,,,,,,,
mondo:0054802,"erythrocytosis, familial, 7","['ECYT7', 'polycythemia, Alpha-globin type', 'erythrocytosis, Alpha-globin type', 'erythrocytosis, FAMILIAL, 7', 'erythrocytosis 7']",0111631,617981,,CN244942,,,,,,,,
mondo:0054804,"microcephaly 21, primary, autosomal recessive","['MCPH21', 'microcephaly 21, PRIMARY, autosomal recessive']",,617983,,CN244930,,,,,,,,
mondo:0054805,"microcephaly 22, primary, autosomal recessive","['MCPH22', 'microcephaly 22, PRIMARY, autosomal recessive']",,617984,,,,,,,,,,
mondo:0054806,"microcephaly 23, primary, autosomal recessive","['MCPH23', 'microcephaly 23, PRIMARY, autosomal recessive']",,617985,,CN244932,,,,,,,,
mondo:0054813,"Ehlers-Danlos syndrome, classic-like, 2","['EDSCLL2', 'Ehlers-Danlos syndrome, classic-like, 2']",0080732,618000,536532,CN248508,"['0.02776', '0.06836', '-0.01677', '-0.01591', '0.0567', '-0.1239', '0.0201', '0.1037', '-0.0785', '-0.002213', '-0.02797', '-0.02373', '0.03326', '-0.003862', '0.002157', '-0.07623', '-0.0348', '0.0211', '0.0473', '-0.1473', '0.00531', '-0.01665', '0.10187', '-0.02469', '0.003777', '-0.02083', '-0.03415', '-0.0315', '0.09467', '-0.03882', '0.119', '-0.01996', '0.0918', '0.0635', '0.02554', '-0.03014', '-0.01031', '0.009995', '-0.03284', '-0.1206', '0.07556', '-0.0595', '0.009285', '-0.011116', '0.00921', '-0.09393', '-0.0302', '0.0792', '0.02272', '0.0238', '-0.0088', '-0.03094', '0.03546', '-0.003696', '-0.0502', '-0.0412', '0.067', '-0.02892', '-0.0268', '-0.005203', '0.04315', '0.02725', '0.0319', '0.00951', '0.00054', '0.01955', '0.06274', '0.06256', '-0.11304', '0.154', '-0.08136', '-0.019', '-0.00067', '-0.0702', '0.04095', '0.00832', '-0.02016', '-0.01373', '-0.07806', '-0.05212', '0.02757', '-0.01765', '-0.0709', '0.0596', '-0.05807', '-0.04718', '0.06024', '0.1224', '0.10876', '0.01932', '0.01171', '0.07965', '0.0208', '0.002321', '0.2021', '0.01923', '0.085', '-0.1302', '-0.02173', '0.01872']",,,,,,,
mondo:0054817,"leukodystrophy, hypomyelinating, 17","['leukodystrophy, hypomyelinating, 17', 'HLD17']",0070404,618006,,CN248514,"['-0.03708', '0.04578', '0.01096', '-0.007484', '0.0271', '-0.0534', '0.000344', '0.063', '-0.05707', '-0.00842', '-0.04303', '-0.01881', '-0.02507', '-0.03088', '0.004715', '-0.03244', '-0.001666', '-0.02716', '-0.02042', '-0.0901', '0.00977', '-0.01736', '0.0452', '-0.02026', '0.02919', '-0.01155', '-0.00676', '-0.01817', '0.01874', '-0.02344', '0.038', '0.01249', '0.0681', '0.001119', '0.03009', '-0.0237', '-0.01151', '-0.02007', '-0.01235', '-0.05344', '0.0393', '-0.0737', '0.01746', '-0.011406', '-0.00861', '-0.03674', '-0.02086', '0.04086', '0.009254', '-0.001452', '0.01313', '0.00298', '-0.02504', '0.00174', '-0.0419', '-0.02245', '0.074', '-0.0234', '-0.0611', '0.02449', '0.02486', '0.02188', '0.0203', '0.00946', '-0.01543', '-0.01325', '0.05927', '0.04297', '-0.0525', '0.0546', '-0.0559', '0.01333', '0.0144', '-0.04053', '0.03333', '0.02023', '-0.00735', '0.000898', '-0.0339', '-0.03378', '-0.01186', '-0.02547', '0.00487', '0.05292', '-0.002176', '0.0001718', '0.02841', '0.06323', '0.04752', '0.001159', '0.03032', '0.05167', '0.0043', '0.02644', '0.10956', '0.04517', '0.054', '-0.07367', '0.00962', '0.01502']",,,,,,,
mondo:0054831,Coffin-Siris syndrome 7,"['COFFIN-SIRIS syndrome 7', 'CSS7']",0112369,618027,,CN248780,,,,,,,,
mondo:0054832,"corneal dystrophy, posterior polymorphous, 4","['corneal dystrophy, POSTERIOR polymorphous, 4', 'PPCD4']",0080669,618031,,CN248531,,,,,,,,
mondo:0054833,"charcot-marie-tooth disease, axonal, type 2DD","['Charcot-Marie-Tooth neuropathy, type 2Dd', 'CMT2DD', 'Charcot-Marie-tooth disease, axonal, type 2DD']",0111558,618036,521414,CN248781,"['-0.0268', '0.0681', '0.01836', '0.002106', '0.01408', '-0.05588', '-0.01291', '0.05054', '-0.04718', '-0.003622', '-0.02066', '-0.009026', '-0.00963', '0.01869', '-0.006786', '-0.043', '-0.007008', '-0.02133', '0.002699', '-0.08026', '0.00684', '-0.01796', '0.0341', '0.01692', '0.00822', '-0.0001749', '-0.006912', '-0.01262', '0.01037', '-0.0199', '0.03665', '-0.01121', '0.06995', '0.02232', '0.04102', '-0.05035', '-0.02422', '-0.01132', '0.002829', '-0.05362', '-0.0282', '-0.0485', '-0.0009475', '0.0004296', '-0.01926', '-0.049', '-0.02023', '0.02946', '0.004013', '0.0009627', '0.012405', '0.006767', '0.01553', '-0.00906', '-0.00749', '-0.03714', '0.03806', '-0.01576', '-0.05496', '-0.01784', '0.01233', '-0.01096', '0.02435', '0.0186', '-0.01177', '0.03207', '0.02628', '0.02864', '-0.0407', '0.034', '-0.03986', '-0.001282', '0.01329', '-0.02493', '0.04797', '0.03001', '-0.007736', '0.01082', '-0.02812', '-0.0406', '-0.01465', '-0.0161', '-0.013435', '0.05457', '-0.002943', '-0.000364', '0.01363', '0.0515', '0.0606', '0.01045', '0.010796', '0.03378', '0.04178', '0.02693', '0.0943', '0.0648', '0.04175', '-0.04633', '-0.02396', '0.0086']",,,,,,,
mondo:0054835,classic dopamine transporter deficiency syndrome,"['classic DTDS', 'PKDYS', 'PKDYS1', 'dopamine transporter deficiency syndrome', 'Parkinsonism-dystonia, infantile, 1']",,613135,,C2751067,,C129866,,,,,,
mondo:0054836,"parkinsonism-dystonia, infantile, 2","['PKDYS2', 'Parkinsonism-dystonia, infantile, 2']",,618049,,CN248785,,,,,,,,
mondo:0054837,"intellectual disability, autosomal dominant 57","['MRD57', 'intellectual disability, autosomal dominant 57', 'intellectual developmental disorder, autosomal dominant 57', 'mental retardation, autosomal dominant 57']",,618050,,CN252334,"['-0.02705', '0.04337', '0.02835', '-0.02933', '0.02782', '-0.04703', '0.001247', '0.05814', '-0.03906', '-0.02022', '-0.0215', '-0.00397', '-0.000797', '0.001765', '-0.003696', '-0.006767', '0.00957', '-0.02531', '-0.01921', '-0.08344', '-0.02267', '-0.01653', '0.03041', '-0.03146', '0.02585', '0.00916', '-0.01884', '-0.0104', '0.01082', '-0.04355', '0.04172', '-0.006958', '0.0508', '0.00585', '0.00217', '-0.00833', '-0.01796', '-0.0246', '-0.01146', '-0.05087', '0.01349', '-0.0453', '0.003096', '-0.01755', '-0.003817', '-0.05008', '-0.02032', '0.02113', '0.00343', '0.02368', '-0.01054', '-0.003176', '-0.004593', '-0.00808', '-0.006287', '-0.04056', '0.0479', '-0.0235', '-0.06415', '0.00926', '0.02983', '0.01182', '0.001791', '0.01678', '0.006023', '0.01376', '0.05496', '0.03726', '-0.05817', '0.0583', '-0.0495', '0.007195', '0.0288', '-0.0346', '0.02364', '0.01909', '0.0007854', '-0.00527', '-0.03665', '-0.01706', '-0.004723', '0.00703', '-0.00739', '0.04572', '-8.51e-05', '0.01517', '0.02211', '0.04837', '0.05164', '0.012024', '0.0188', '0.04642', '-0.00884', '0.0161', '0.097', '0.03476', '0.0565', '-0.05597', '0.0122', '0.0283']",,,,,,,
mondo:0054838,"cardiomyopathy, familial hypertrophic 27","['cardiomyopathy, FAMILIAL hypertrophic 27', 'CMH27']",,618052,,CN252335,,,,,,,,
mondo:0054842,polycystic kidney disease 6 with or without polycystic liver disease,"['PKD6', 'DNAJB11 polycystic kidney disease', 'polycystic kidney disease 6 with or without polycystic liver disease']",,618061,,CN252647,"['0.01349', '0.0955', '4.49e-05', '-0.03378', '0.0504', '-0.12427', '-0.0316', '0.1295', '-0.06287', '-0.02815', '-0.06647', '-0.03882', '0.000976', '0.03897', '-0.1064', '-0.1373', '-0.0172', '0.002964', '-0.03047', '-0.1985', '0.02144', '-0.0725', '0.09467', '-0.02216', '0.04065', '-0.09296', '0.02011', '-0.006794', '0.074', '-0.04114', '0.128', '-0.0185', '0.1278', '0.0186', '0.01429', '-0.0804', '-0.06696', '-0.06683', '-0.03036', '-0.05734', '0.00859', '-0.0696', '0.0752', '-0.02107', '-0.05493', '-0.09863', '-0.03137', '0.07263', '-0.05197', '0.0741', '-0.05603', '0.02795', '0.03833', '0.003517', '-0.03497', '-0.05914', '0.10004', '-0.05695', '-0.1788', '-0.01602', '0.1241', '0.06506', '0.01059', '0.01692', '0.003563', '-0.04904', '0.1114', '0.1007', '-0.129', '0.10535', '-0.05655', '-0.01614', '0.03943', '-0.09143', '0.0579', '0.006607', '0.004192', '0.02779', '-0.09033', '-0.0466', '-0.02449', '0.01244', '-0.0367', '0.04636', '-0.01415', '0.011185', '0.05063', '0.0946', '0.0815', '0.03726', '0.01743', '0.08777', '0.00279', '0.03867', '0.254', '0.0438', '0.075', '-0.1559', '-0.0485', '0.0423']",,,,,,,
mondo:0054843,"ciliary dyskinesia, primary, 38","['ciliary dyskinesia, PRIMARY, 38', 'ciliary dyskinesia, Primary, 38, with or without situs inversus', 'CILD38']",0111852,618063,,CN252651,,,,,,,,
mondo:0054844,"pontocerebellar hypoplasia, type 1D","['pontocerebellar hypoplasia, type 1D', 'PCH1D']",0112323,618065,,CN252648,,,,,,,,
mondo:0054845,"developmental and epileptic encephalopathy, 66","['DEE66', 'EIEE66', 'developmental and epileptic encephalopathy 66', 'epileptic encephalopathy, early infantile, 66']",0080446,618067,,CN252658,"['-0.002398', '0.05756', '-0.01335', '-0.0009246', '0.006325', '-0.083', '0.02312', '0.0662', '-0.063', '-0.01572', '-0.0604', '-0.02397', '-0.010925', '-0.005997', '0.0001044', '-0.0556', '-0.012505', '-0.03748', '-0.03192', '-0.12177', '-0.002985', '-0.0301', '0.0412', '-0.03964', '0.01884', '-0.01807', '-0.02022', '-0.01276', '-0.02574', '-0.02078', '0.05438', '-0.00253', '0.0691', '0.02783', '0.01645', '-0.00805', '-0.02174', '-0.02736', '-0.0224', '-0.04184', '0.03342', '-0.09247', '0.02254', '-0.02617', '-0.01429', '-0.05493', '-0.011475', '0.04617', '-0.009285', '0.04285', '-0.00457', '-0.002523', '-0.00952', '0.007366', '-0.00839', '-0.03323', '0.05856', '-0.04965', '-0.0667', '0.03445', '0.03586', '0.02338', '0.02298', '0.00876', '-0.00562', '-0.01056', '0.07776', '0.04916', '-0.0655', '0.05774', '-0.05435', '0.02304', '0.0092', '-0.02966', '0.02567', '0.04492', '0.02814', '-0.02', '-0.04462', '-0.03876', '-0.002993', '0.01061', '-0.0524', '0.04318', '0.01767', '0.01723', '0.02325', '0.04672', '0.09924', '0.01974', '0.04205', '0.06836', '0.005913', '0.0178', '0.1098', '0.0566', '0.05573', '-0.07935', '0.01416', '0.00366']",,,,,,,
mondo:0054846,"epilepsy, familial adult myoclonic, 6","['FAME6', 'epilepsy, FAMILIAL ADULT myoclonic, 6', 'cortical myoclonic tremor with epilepsy, Familial, 6', 'benign Adult Familial myoclonic epilepsy 6']",0111696,618074,,CN252655,,,,,,,,
mondo:0054847,"epilepsy, familial adult myoclonic, 7","['cortical myoclonic tremor with epilepsy, Familial, 7', 'epilepsy, FAMILIAL ADULT myoclonic, 7', 'FAME7', 'benign Adult Familial myoclonic epilepsy 7']",0111694,618075,,CN252654,,,,,,,,
mondo:0054849,inflammatory bowel disease 29,"['inflammatory bowel disease 29', 'IBD29']",0112155,618077,,,,,,,,,,
mondo:0054850,ovarian dysgenesis 6,"['ODG6', 'ovarian dysgenesis 6']",0080498,618078,,,,,,,,,,
mondo:0054852,peeling skin syndrome 6,"['peeling skin syndrome 6', 'PSS6']",,618084,,,"['0.0181', '0.11383', '0.00818', '0.0153', '0.0791', '-0.1394', '-0.00854', '0.06647', '-0.0776', '-0.04984', '-0.0389', '0.04532', '0.01566', '-0.008026', '-0.02997', '-0.03079', '0.05295', '-0.00558', '-0.00835', '-0.1785', '-0.04758', '-0.03494', '0.0564', '-0.037', '0.03238', '0.002413', '-0.0567', '-0.02213', '-0.00805', '-0.08356', '0.0826', '-0.003685', '0.083', '0.03955', '0.03397', '-0.0123', '-0.05548', '-0.0525', '-0.02164', '-0.0635', '0.0588', '-0.1737', '0.02873', '-0.06525', '-0.01014', '-0.0941', '-0.08606', '0.10223', '0.011215', '0.01607', '-0.0887', '-0.02757', '0.0468', '0.03375', '-0.07715', '-0.0008416', '0.1113', '-0.02959', '-0.12384', '-0.045', '0.06055', '0.05685', '-0.01114', '0.01223', '0.02129', '0.00242', '0.1573', '0.0862', '-0.10065', '0.1553', '-0.1272', '-0.01108', '0.01299', '-0.06216', '0.03775', '0.05334', '-0.029', '-0.01417', '-0.0711', '-0.1046', '-0.00836', '-0.01258', '-0.03226', '0.0902', '-0.00804', '-0.01458', '0.0378', '0.1499', '0.1151', '0.01033', '0.075', '0.08716', '0.0591', '0.05792', '0.2091', '0.02937', '0.06396', '-0.1643', '0.01958', '0.00508']",,,,,,,
mondo:0054860,"hearing loss, autosomal recessive 110","['deafness, autosomal recessive 110', 'DFNB110']",0111644,618094,,,"['-0.01305', '0.0381', '0.0096', '-0.00453', '0.0241', '-0.0508', '0.0002763', '0.066', '-0.0336', '-0.0233', '-0.01005', '-0.006992', '0.001607', '0.001874', '-0.01525', '-0.0277', '0.0159', '-0.02396', '-0.00918', '-0.0761', '-0.03128', '-0.01492', '0.02095', '-0.02261', '0.00686', '-0.007812', '-0.01627', '-0.013084', '0.013626', '-0.0287', '0.02444', '0.01491', '0.03873', '0.03079', '0.003716', '-0.02116', '-0.01752', '-0.03027', '0.004795', '-0.04987', '0.01854', '-0.04272', '0.01189', '0.001335', '-0.00643', '-0.0524', '-0.008965', '0.03915', '0.00592', '0.0237', '-0.011536', '-0.01854', '-0.001162', '0.0008106', '-0.01646', '-0.0275', '0.0418', '-0.01319', '-0.0647', '0.01019', '0.03076', '0.0354', '0.002073', '0.01101', '-0.00587', '-0.007027', '0.05005', '0.032', '-0.05127', '0.05655', '-0.03592', '0.018', '0.02626', '-0.04605', '0.0334', '0.02385', '-0.002031', '0.00223', '-0.04065', '-0.01083', '0.002369', '0.000929', '-0.003803', '0.03824', '0.002602', '0.01414', '0.01741', '0.04822', '0.04233', '0.02591', '0.02711', '0.04797', '-0.00842', '0.01646', '0.1002', '0.0333', '0.04694', '-0.0616', '-0.01219', '0.03152']",,,,,,,
mondo:0054861,"intellectual disability, autosomal recessive 63","['MRT63', 'mental retardation, autosomal recessive 63', 'intellectual disability, autosomal recessive 63']",0081224,618095,,,,,,,,,,
mondo:0054862,premature ovarian failure 15,"['premature ovarian failure 15', 'POF15']",0080872,618096,,,,,,,,,,
mondo:0054865,encephalopathy due to mitochondrial and peroxisomal fission defect,"['encephalopathy due to mitochondrial and peroxisomal fission defect', 'encephalopathy due to defective mitochondrial and peroxisomal fission']",,,527276,,,,,,,,,
mondo:0054866,sudden arrhythmia death syndrome,"['sudden arrhythmic death syndrome', 'sudden cardiac death due to cardiac arrhythmia', 'SADS']",,,,C2721586,,,,,,,,
mondo:0054867,paraomphalocele,"['Paraomphalocele, hypogastric', 'Paraomphalocele, epigastric']",,,,,,,,C537170,,,,
mondo:0054868,meconium ileus,['meconium ileus'],,,,,,C98979,,D000074270,,,,
mondo:0054869,nondystrophic myotonia,['NDM'],,,,,,,,C536245,,,,
mondo:0056795,X-linked spermatogenic failure 1,"['Del Castillo syndrome', 'Germinal cell aplasia', 'spermatogenic failure, X-linked, 1', 'spermatogenic failure, X-linked, type 1', 'SPGFX1', 'Sertoli cell-only syndrome']",0070189,305700,,,,,,,,,,
mondo:0056796,obstructive nephropathy,['congenital obstructive nephropathy'],0070314,,,C0149939,,C120902,,,593.89,,,
mondo:0056797,neurodevelopmental disorder with midbrain and hindbrain malformations,"['neurodevelopmental disorder with midbrain and hindbrain malformations', 'NEDMHM']",0080312,617523,,C4479613,"['-0.04404', '0.0492', '0.01359', '-0.03732', '0.02237', '-0.06775', '0.01872', '0.07935', '-0.0688', '-0.04333', '-0.03012', '-0.01752', '-0.006073', '0.01959', '-0.03464', '-0.0345', '-0.005398', '-0.02777', '-0.0521', '-0.1149', '-0.00012076', '-0.01323', '0.0546', '-0.03198', '0.01473', '-0.02425', '0.00144', '-0.006126', '0.03235', '-0.03766', '0.02457', '-0.005295', '0.09973', '0.04834', '0.02655', '-0.01182', '-0.005745', '-0.02995', '-0.014496', '-0.06915', '0.03397', '-0.0705', '0.00332', '-0.01485', '-0.0004692', '-0.06915', '-0.02422', '0.0402', '-0.007618', '0.04703', '-0.03146', '0.01506', '0.0182', '-0.005806', '-0.02136', '-0.022', '0.0498', '-0.004253', '-0.0833', '0.01218', '0.02477', '0.01418', '0.01907', '0.02522', '-0.002527', '0.00781', '0.0856', '0.06198', '-0.0555', '0.06757', '-0.07947', '0.01083', '0.01208', '-0.02812', '0.01211', '0.02824', '0.0185', '-0.00901', '-0.03745', '-0.04648', '-0.00611', '-0.01158', '-0.01134', '0.07404', '-0.003836', '0.004654', '-0.0005617', '0.0543', '0.0697', '0.01721', '0.029', '0.0726', '-0.006916', '0.0379', '0.1229', '0.0403', '0.0783', '-0.0955', '0.014565', '0.04834']",,,,,,,
mondo:0056798,disorder of appendix,"['disorder of vermiform appendix', 'disease of vermiform appendix', 'vermiform appendix disease or disorder']",60000,,,C0267613,,,,,543.9,K35-K38,,
mondo:0056799,synovium disorder,"['layer of synovial tissue disease or disorder', 'disorder of layer of synovial tissue', 'disease of layer of synovial tissue']",,,,C0263945,,,,,727.9,,,
mondo:0056802,synovial bursa disorder,"['disease of synovial bursa', 'synovial bursa disease or disorder', 'disorder of synovial bursa']",,,,C0263946,,,,,,,,
mondo:0056803,sulfur metabolism disease,"['disorder of sulfur compound metabolic process', 'disorder of sulphur metabolic process', 'disorder of sulphur metabolism', 'disorder of sulphur compound metabolic process', 'sulphur compound metabolic process disease']",,,,C1263724,,,,,,,,
mondo:0056804,benign neoplasm of peripheral nervous system,,0080320,,,,,,,,,,,
mondo:0056805,benign peripheral nerve granular cell tumor,"['benign granular cell neoplasm of peripheral nerve', 'benign peripheral nerve granular cell neoplasm', 'benign granular cell tumour of the peripheral nerve', 'nerve benign granular cell tumor', 'benign granular cell tumor of the peripheral nerve', 'benign granular cell neoplasm of the peripheral nerve', 'benign granular cell tumour of nerve', 'nerve benign granular cell tumour', 'benign granular cell tumor of peripheral nerve', 'benign granular cell tumour of peripheral nerve', 'benign peripheral nerve granular cell tumor']",,,,C1332530,,C5502,,,,,,
mondo:0056806,non-small cell squamous lung carcinoma,"['non-small cell squamous lung cancer', 'non-small cell squamous lung carcinoma', 'squamous non-small cell lung carcinoma']",0080521,,,,,C133254,,,,,,
mondo:0056813,hormone-resistant breast carcinoma,"['hormone-refractory breast cancer', 'hormone-resistant breast carcinoma', 'hormone-resistant breast cancer']",,,,,,C114932,,,,,,
mondo:0056814,hormone-resistant prostate carcinoma,"['hormone-resistant prostate cancer', 'hormone-resistant prostate carcinoma']",,,,,,C114933,,,,,,
mondo:0056815,liver adenosquamous carcinoma,"['liver adenosquamous carcinoma', 'liver adenosquamous cancer']",,,,C3898586,,C118630,,,,,,
mondo:0056816,vulvar neuroendocrine carcinoma,"['vulvar Neuroendocrine cancer', 'vulvar high grade Neuroendocrine carcinoma', 'vulvar high grade Neuroendocrine neoplasm', 'vulvar Neuroendocrine carcinoma', 'mammalian vulva neuroendocrine carcinoma']",,,,C4288002,,C128243,,,,,,
mondo:0056817,rectal adenosquamous carcinoma,"['rectal adenosquamous cancer', 'rectal adenosquamous carcinoma']",,,,C1709865,,C43594,,,,,,
mondo:0056818,skin adenosquamous carcinoma,"['skin adenosquamous cancer', 'skin adenosquamous carcinoma']",,,,C1710103,,C54250,,,,,,
mondo:0056819,nasal cavity and paranasal sinus carcinoma,"['sinonasal carcinoma', 'paranasal sinus and nasal cavity cancer', 'nasal cavity and paranasal sinus carcinoma', 'nasal cavity and paranasal sinus cancer']",,,,C1710095,,C54293,,,,,,
mondo:0056820,nasal cavity and paranasal sinus neoplasm,['nasal cavity and paranasal sinus neoplasm'],,,,C1334925,,C7336,,,,,,
mondo:0056822,amyotonia congenita,"['amyotonia congenita', 'Oppenheim disease']",,205000,,,,,,,,,,
mondo:0060455,X-linked congenital hemolytic anemia,"['hemolytic anemia, congenital, X-linked, X-linked recessive', 'hemolytic anemia, congenital, X-linked']",0111846,301015,,,,,,,,,,
mondo:0060456,"cerebral sclerosis, diffuse, scholz type","['cerebral sclerosis, diffuse, scholz type']",,302700,,,,,,C564449,,,,
mondo:0060457,autoinflammation with arthritis and dyskeratosis,"['AUTOINFLAMMATION with arthritis and dyskeratosis', 'AIADK']",,617388,,,"['-0.05573', '0.04422', '-0.00454', '-0.03616', '0.0283', '-0.0998', '0.00734', '0.04694', '-0.0643', '-0.03293', '-0.010056', '-0.01475', '0.002472', '0.0075', '-0.0389', '-0.03235', '0.0317', '-0.0257', '-0.04346', '-0.1268', '-0.01196', '-0.05823', '0.07007', '-0.0527', '0.02567', '0.0118', '-0.01701', '-0.00754', '0.02818', '-0.0428', '0.03772', '-0.0167', '0.0761', '0.04437', '0.02896', '-0.02124', '-0.05362', '-0.03613', '-0.001525', '-0.06445', '0.00575', '-0.0828', '0.00876', '-0.0335', '0.003695', '-0.0728', '-0.0281', '0.05682', '0.01131', '0.0475', '-0.01941', '0.01529', '0.012085', '0.04453', '-0.0343', '-0.0421', '0.05026', '-0.04276', '-0.10034', '-0.00513', '0.0605', '0.0479', '-0.02583', '-0.005157', '0.02419', '0.0084', '0.0831', '0.06824', '-0.05338', '0.09357', '-0.08044', '-0.003937', '0.02888', '-0.0527', '0.02423', '0.02086', '0.003595', '0.006184', '-0.03387', '-0.0455', '-0.00831', '0.00491', '-0.03433', '0.0772', '-0.01938', '0.01318', '-0.00709', '0.0542', '0.06244', '0.02681', '0.03635', '0.04114', '-0.001608', '0.04175', '0.1292', '0.04443', '0.09784', '-0.07745', '-0.01846', '-0.014786']",,,,,,,
mondo:0060486,"arthrogryposis multiplex congenita 1, neurogenic, with myelin defect","['arthrogryposis multiplex congenita, neurogenic, with myelin defect', 'AMCNMY']",0080978,617468,,,,,,,,,,
mondo:0060489,"46,XX sex reversal 4","['46,XX SEX reversal 4', 'SRXX4', '46, XX sex reversal 4', '46,XX Sex reversal, Sry-Negative']",0111764,617480,,,,,,,,,,
mondo:0060490,"neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies","['neurodevelopmental disorder with microcephaly, hypotonia, and variable brain anomalies', 'NMIHBA']",,617481,544469,C4479566,"['-0.06042', '0.0808', '0.03983', '-0.06128', '0.0216', '-0.0746', '0.012184', '0.1259', '-0.11536', '-0.04587', '-0.0507', '-0.03027', '0.002111', '-0.00589', '-0.03714', '-0.04327', '0.013306', '-0.03586', '-0.0914', '-0.1937', '0.012184', '-0.0348', '0.0681', '-0.03326', '0.05014', '-0.05652', '-0.002186', '0.00598', '0.0184', '-0.0466', '0.0551', '-0.03024', '0.138', '0.0655', '0.00919', '-0.003513', '-0.04013', '-0.04425', '-0.01723', '-0.08734', '0.05533', '-0.0874', '0.01631', '-0.03012', '0.003067', '-0.09155', '-0.005703', '0.06537', '-0.03552', '0.03998', '-0.045', '0.02127', '-0.02087', '-0.00122', '-0.02664', '-0.02348', '0.04263', '-0.02158', '-0.1045', '0.0387', '0.05197', '0.02637', '-0.01118', '0.03488', '-0.01678', '0.00971', '0.087', '0.0957', '-0.1039', '0.11426', '-0.09406', '0.04868', '0.02942', '-0.0384', '0.01276', '0.03854', '0.05707', '-0.03357', '-0.0537', '-0.0384', '0.01556', '-0.005596', '-0.039', '0.1195', '0.002201', '0.00896', '0.011116', '0.0979', '0.1147', '0.05133', '0.05392', '0.11786', '-0.01293', '0.03238', '0.1646', '0.0705', '0.1075', '-0.0952', '0.05923', '0.03094']",,,,,,,
mondo:0060491,neurodevelopmental disorder with involuntary movements,"['NEDIM', 'neurodevelopmental disorder with involuntary movements']",0112276,617493,,,"['-0.07025', '0.08887', '0.04288', '-0.04074', '0.01697', '-0.08594', '0.04172', '0.08417', '-0.08405', '-0.05432', '-0.012794', '-0.02896', '-0.003809', '0.0363', '-0.001675', '-0.006035', '0.005566', '-0.02109', '-0.00841', '-0.1937', '0.00881', '-0.0223', '0.04138', '-0.03516', '0.02744', '-0.0206', '-0.0229', '-0.00689', '0.004105', '-0.0469', '0.02135', '-0.006355', '0.0976', '0.04108', '0.001257', '-0.01563', '-0.02072', '-0.05533', '-0.01732', '-0.0901', '0.04407', '-0.0811', '-0.03134', '-0.02257', '0.02182', '-0.1027', '-0.01717', '0.0766', '0.01788', '0.08746', '-0.0832', '-0.01309', '-0.002478', '-0.01164', '0.01154', '-0.03305', '0.03888', '-0.02647', '-0.089', '-0.02211', '0.0365', '0.04413', '0.02753', '-0.0327', '-0.03516', '0.006935', '0.11914', '0.0782', '-0.04932', '0.05795', '-0.03513', '0.02065', '-0.002043', '-0.03452', '0.02863', '0.04254', '0.02087', '-0.00599', '-0.0516', '-0.0253', '0.02304', '0.003418', '-0.02005', '0.10846', '0.00414', '0.007835', '0.03952', '0.102', '0.09644', '0.06287', '0.01913', '0.0997', '0.0326', '0.0641', '0.1726', '0.0656', '0.04813', '-0.06232', '0.04922', '0.0654']",,,,,,,
mondo:0060496,"neurodevelopmental disorder with hypotonia, neuropathy, and deafness","['NEDHND', 'neurodevelopmental disorder with hypotonia, neuropathy, and deafness', 'myopathy, Congenital, with neuropathy and Deafness']",,617519,,C4479603,,,,,,,,
mondo:0060502,"neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies","['neurodevelopmental disorder with progressive microcephaly, spasticity, and brain anomalies', 'NDMSBA']",,617527,521426,C4479631,"['-0.06396', '0.0835', '0.02995', '-0.05658', '0.02507', '-0.08887', '0.017', '0.1165', '-0.11743', '-0.03723', '-0.02373', '-0.03772', '-0.00896', '0.01678', '-0.003014', '-0.04474', '0.0138', '-0.0322', '-0.07324', '-0.1766', '0.01491', '-0.02481', '0.04916', '-0.02866', '0.03885', '-0.0437', '0.00746', '0.00236', '-0.00492', '-0.0488', '0.05466', '-0.003094', '0.1154', '0.0337', '0.02493', '-0.01755', '-0.01578', '-0.03497', '-0.01735', '-0.0669', '0.0386', '-0.0939', '0.00616', '-0.01851', '0.002058', '-0.086', '-0.03378', '0.06076', '-0.00877', '0.0263', '-0.04202', '0.01888', '-0.012726', '0.00849', '-0.0202', '-0.01785', '0.0648', '-0.02429', '-0.1034', '0.024', '0.02907', '0.03757', '0.02174', '0.03607', '-0.03836', '0.02522', '0.08545', '0.0673', '-0.0795', '0.09753', '-0.06885', '0.04282', '0.02206', '-0.0581', '0.02734', '0.0326', '0.02383', '-0.03108', '-0.05157', '-0.0585', '0.01675', '-0.007305', '-0.01474', '0.1085', '-0.02022', '0.01846', '0.000586', '0.0762', '0.0776', '0.04062', '0.04556', '0.1131', '0.00462', '0.02602', '0.152', '0.0479', '0.0882', '-0.0683', '0.04324', '0.0604']",,,,,,,
mondo:0060507,retinal dystrophy with or without macular staphyloma,"['retinal dystrophy with or without macular staphyloma', 'retinal dystrophy with macular staphyloma', 'RDMS']",,617547,,C4479651,"['-0.0509', '0.03072', '0.006744', '-0.01256', '0.03577', '-0.1007', '0.00333', '0.06665', '-0.06775', '-0.05304', '-0.02847', '-0.03308', '-0.036', '0.01438', '-0.02744', '-0.0654', '0.03903', '-0.04855', '-0.01749', '-0.17', '-0.02473', '-0.02428', '0.0475', '0.02887', '0.02107', '-0.00408', '-0.01175', '-0.02487', '-0.003113', '-0.003584', '0.06976', '-0.02066', '0.0843', '0.01697', '0.02914', '0.01674', '-0.02063', '-0.03348', '-0.01068', '-0.1085', '0.0531', '-0.08356', '0.01967', '-0.01472', '-0.02718', '-0.04074', '-0.01179', '0.05673', '0.001199', '0.02908', '0.005547', '0.01802', '0.0313', '0.003284', '-0.02971', '-0.03363', '0.0915', '-0.0324', '-0.1317', '-0.0184', '0.04474', '0.01578', '0.01554', '0.0275', '0.0081', '-0.0129', '0.12177', '0.0884', '-0.06415', '0.0902', '-0.0585', '0.00561', '0.01375', '-0.03693', '0.05948', '0.02036', '-0.00109', '-0.01729', '-0.04788', '-0.0596', '0.02638', '4.38e-05', '0.001003', '0.0988', '-0.03503', '-0.03217', '0.001383', '0.0878', '0.09454', '0.01738', '0.01846', '0.0683', '-0.005386', '0.06186', '0.1454', '0.02478', '0.05792', '-0.0946', '-0.02318', '0.05087']",,,,,,,
mondo:0060510,Cohen-Gibson syndrome,"['COGIS', 'Cohen-Gibson syndrome']",,617561,,C4479654,"['-0.00824', '0.02374', '0.01431', '-0.00893', '0.011215', '-0.03357', '0.00855', '0.01888', '-0.02925', '-0.02162', '-0.001187', '-0.00161', '0.00704', '-0.003075', '0.000998', '-0.02388', '-0.01178', '0.001783', '-0.01121', '-0.04178', '0.0003815', '-0.007565', '0.01653', '-0.011734', '0.005558', '0.000931', '-0.00623', '0.00679', '0.01049', '-0.01084', '0.02063', '0.002665', '0.02415', '0.01021', '-0.004055', '-0.01155', '0.00655', '-0.010475', '0.00589', '-0.02173', '0.002096', '-0.02197', '-0.00656', '-0.00872', '0.01243', '-0.011154', '-0.01584', '0.00866', '0.007675', '0.01461', '-0.01472', '-0.006508', '-0.007477', '-0.002878', '-0.01959', '-0.00756', '0.01619', '-0.007393', '-0.02238', '0.0005655', '0.003845', '0.01022', '-0.000365', '-0.011345', '0.00387', '0.01091', '0.02571', '0.002497', '-0.0251', '0.02098', '-0.01672', '0.010506', '0.001725', '-0.0086', '0.001607', '0.00777', '0.00946', '-0.007072', '-0.01332', '-0.01295', '0.0008593', '-0.00169', '-0.005154', '0.0188', '-0.00941', '-0.003628', '-0.002316', '0.01249', '0.03072', '0.00916', '0.01764', '0.01953', '-0.002773', '0.006348', '0.04593', '0.018', '0.02045', '-0.03622', '-0.00118', '0.0128']",,,,,,,
mondo:0060527,maleylacetoacetate isomerase deficiency,"['hypersuccinylacetonemia, mild', 'benign hypersuccinylacetonemia', 'MAAID', 'maleylacetoacetate isomerase deficiency', 'MAAI deficiency']",,617596,,C1291607,"['-0.0353', '0.0456', '0.005966', '-0.00688', '0.02896', '-0.05328', '-0.00247', '0.03354', '-0.03192', '-0.0372', '-0.00571', '0.001776', '0.00492', '0.00965', '-0.01408', '-0.01906', '-0.00924', '-0.02264', '-0.03482', '-0.06586', '-0.01743', '-0.01874', '0.04434', '-0.00049', '-9.966e-05', '-0.00906', '0.00696', '-0.01432', '0.01596', '-0.03683', '0.02731', '0.01502', '0.03925', '0.02863', '0.00894', '-0.03653', '-0.002022', '-0.03473', '-0.01024', '-0.04102', '0.01726', '-0.05283', '0.01944', '-0.01177', '-0.01662', '-0.0542', '0.003592', '0.02367', '0.01906', '0.01189', '-0.02095', '-0.01091', '0.0167', '0.02446', '-0.0177', '-0.01271', '0.0438', '-0.006313', '-0.0697', '0.01595', '0.02853', '0.02362', '0.02954', '0.002802', '0.011314', '-0.007393', '0.0399', '0.0217', '-0.02805', '0.0471', '-0.02405', '-0.006535', '-0.005318', '-0.02727', '0.02533', '0.01677', '0.02167', '-0.01533', '-0.01917', '-0.015175', '0.002384', '-0.006695', '-0.02144', '0.02893', '0.01828', '-0.01418', '0.009186', '0.02992', '0.073', '0.002842', '0.02028', '0.04327', '-0.011566', '0.00415', '0.0848', '0.04706', '0.03033', '-0.0546', '-0.01117', '0.005196']",,,,,,,
mondo:0060532,congenital heart defects and skeletal malformations syndrome,"['CHDSKM', 'congenital heart defects and skeletal malformations syndrome', 'marfanoid habitus-facial dysmorphism-skeletal abnormality-heart defect syndrome']",,617602,643503,C4539857,"['-0.05264', '0.03674', '0.05917', '-0.0354', '0.08185', '-0.0952', '0.03702', '0.12476', '-0.07996', '-0.07684', '-0.0376', '-0.0462', '0.005768', '0.03784', '-0.0831', '-0.0499', '-0.0338', '-0.05075', '-0.08954', '-0.1808', '0.02019', '-0.01258', '0.1039', '-0.04236', '0.06415', '-0.02126', '-0.01252', '-0.01378', '0.08844', '-0.04965', '0.1113', '-0.02103', '0.1366', '0.05948', '0.0508', '-0.04034', '0.00581', '-0.03348', '-0.01113', '-0.09235', '0.05743', '-0.0809', '0.03128', '-0.0242', '0.01542', '-0.1063', '-0.04034', '0.11206', '-0.01183', '0.0519', '-0.0834', '0.005714', '0.04962', '-0.006668', '-0.06494', '-0.05695', '0.06305', '0.01168', '-0.11633', '-0.0103', '0.0623', '0.03705', '-0.02701', '0.004047', '-0.03', '0.009796', '0.1061', '0.1225', '-0.1309', '0.0967', '-0.0897', '0.02054', '0.02472', '-0.05258', '0.04852', '0.01944', '0.02132', '-0.0528', '-0.0848', '-0.0689', '-0.01984', '-0.02307', '-0.01121', '0.0968', '-0.0391', '-0.00607', '0.04608', '0.0915', '0.0889', '0.0342', '0.03305', '0.09924', '0.03412', '0.07227', '0.2167', '0.0508', '0.1633', '-0.144', '-0.002684', '0.04947']",,,,,,,
mondo:0060533,"microcephaly, short stature, and limb abnormalities","['MISSLA', 'microcephaly, short stature, and limb abnormalities']",,617604,572773,C4539873,"['-0.09576', '0.1108', '0.0742', '-0.1282', '0.0789', '-0.1032', '0.03455', '0.207', '-0.1793', '-0.10156', '-0.0092', '0.04105', '-0.015045', '0.03833', '-0.06836', '-0.0643', '0.04742', '-0.03714', '-0.1279', '-0.2283', '0.03564', '0.01249', '0.05225', '-0.05212', '0.0624', '-0.0344', '0.0004597', '-0.0102', '0.010376', '-0.05695', '0.09705', '-0.07294', '0.1478', '0.07355', '0.04282', '0.01819', '-0.04315', '-0.0766', '-0.05466', '-0.08575', '0.08966', '-0.10394', '0.03705', '-0.02786', '0.00543', '-0.1251', '-0.002716', '0.1205', '0.0388', '-0.006535', '-0.05716', '-0.03958', '-0.01811', '-0.01014', '-0.06174', '-0.1165', '-0.00507', '-0.09796', '-0.11316', '-0.001205', '0.0789', '-0.009674', '-0.06573', '0.0768', '-0.0719', '-0.001519', '0.1041', '0.1204', '-0.1566', '0.11615', '-0.1624', '0.069', '0.0987', '-0.0909', '0.00745', '0.00587', '0.0358', '-0.0876', '-0.0764', '-0.1054', '-0.0102', '-0.01177', '-0.0322', '0.1393', '-0.06235', '0.07043', '0.00987', '0.1119', '0.1951', '0.03693', '-0.00889', '0.144', '-0.002928', '0.05322', '0.257', '0.0328', '0.11707', '-0.141', '0.0673', '0.0851']",,,,,,,
mondo:0060549,"congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay","['congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay', 'CAKUTHED']",0112359,617641,,C4539968,"['-0.0243', '0.07806', '0.08044', '-0.06128', '0.0485', '-0.0909', '0.00926', '0.2075', '-0.11304', '-0.03995', '-0.04855', '-0.0794', '-0.0527', '0.04163', '-0.1163', '-0.0669', '-0.004818', '-0.0605', '-0.05557', '-0.2363', '0.02275', '-0.0643', '0.06696', '-0.056', '0.07245', '-0.0667', '-0.05618', '0.01808', '0.037', '-0.08295', '0.1194', '-0.0512', '0.1404', '0.05792', '0.02', '-0.05527', '-0.0769', '-0.0357', '-0.02942', '-0.1296', '0.04538', '-0.06384', '0.0559', '-0.02051', '-0.02272', '-0.1384', '-0.01875', '0.06836', '-0.02156', '0.10614', '-0.09827', '0.04037', '0.05148', '-0.02429', '-0.0763', '-0.05212', '0.0582', '-0.04254', '-0.1726', '0.01363', '0.05164', '0.0473', '-0.05005', '0.03665', '-0.01296', '-0.02077', '0.1125', '0.1473', '-0.1147', '0.1262', '-0.08636', '0.0646', '0.04013', '-0.0819', '0.04834', '0.03433', '0.0507', '0.0047', '-0.09033', '-0.05762', '-0.012085', '-0.04385', '-0.000602', '0.1354', '-0.02802', '-0.02483', '0.01454', '0.09753', '0.1335', '0.05566', '0.05875', '0.1621', '-0.01578', '0.05844', '0.2727', '0.0931', '0.1116', '-0.1609', '0.02882', '0.1153']",,,,,,,
mondo:0060550,"polydactyly, postaxial, type a7","['polydactyly, postaxial, type A7', 'PAPA7']",,617642,,,,,,,,,,
mondo:0060551,"cerebellar atrophy, developmental delay, and seizures","['CADEDS', 'cerebellar atrophy, developmental delay, and seizures']",,617643,,C4539985,"['-0.03674', '0.03387', '0.01155', '-0.02261', '0.01991', '-0.0585', '0.00954', '0.0783', '-0.0584', '-0.03644', '-0.03333', '-0.0314', '-0.006374', '0.00773', '-0.01092', '-0.02054', '0.006756', '-0.03378', '-0.02782', '-0.10144', '0.00852', '-0.01385', '0.03516', '-0.01808', '0.03275', '-0.02576', '-0.00241', '-0.003572', '0.004726', '-0.03177', '0.034', '-0.009125', '0.0627', '0.00965', '0.009224', '-0.01031', '-0.01846', '-0.01331', '-0.01479', '-0.03442', '0.01598', '-0.04727', '0.01634', '0.00817', '-0.004192', '-0.0429', '-0.01209', '0.02164', '0.003107', '0.02388', '-0.01293', '0.001112', '0.008934', '0.001751', '-0.02118', '-0.01085', '0.0429', '-0.0218', '-0.06555', '0.02449', '0.01926', '0.02019', '0.004116', '0.003254', '-0.01794', '-0.002913', '0.0523', '0.0651', '-0.05066', '0.05612', '-0.04156', '0.03098', '0.01355', '-0.03586', '0.00452', '0.02942', '0.03014', '-0.02455', '-0.02663', '-0.01469', '0.01141', '-0.004646', '-0.0178', '0.05203', '-0.012054', '0.001107', '0.00892', '0.046', '0.0559', '0.01351', '0.02635', '0.0562', '-0.012276', '0.01837', '0.0864', '0.04297', '0.04263', '-0.03424', '0.01358', '0.02205']",,,,,,,
mondo:0060554,"vertebral, cardiac, renal, and limb defects syndrome 1","['3-hydroxyanthranilic acidemia', 'congenital NAD deficiency Disorder 1', 'VCRL1', 'vertebral, cardiac, renal, and limb defects syndrome 1']",,617660,,C4540004,,,,,,,,
mondo:0060555,"vertebral, cardiac, renal, and limb defects syndrome 2","['kynureninase deficiency, complete', 'congenital NAD deficiency disorder 2', 'vertebral, cardiac, renal, and limb defects syndrome 2', 'VCRL2']",,617661,,C4540014,,,,,,,,
mondo:0060556,"joint laxity, short stature, and myopia","['JLSM', 'joint laxity, short stature, and myopia']",,617662,527450,C4540020,"['-0.0429', '0.03522', '0.02007', '-0.02116', '0.0308', '-0.0655', '0.01147', '0.0806', '-0.0508', '-0.0389', '-0.002651', '0.01286', '-0.0073', '0.01479', '-0.02986', '-0.01508', '0.02153', '-0.025', '-0.03647', '-0.09326', '0.003069', '0.001623', '0.02986', '-0.00935', '0.0228', '-0.00643', '-0.01613', '-0.012314', '-0.001417', '-0.03207', '0.0352', '-0.0434', '0.0569', '0.02101', '0.01685', '-0.02235', '-0.01286', '-0.03105', '-0.01011', '-0.06647', '0.0277', '-0.05154', '-0.00202', '0.0002599', '-0.00258', '-0.0462', '0.00549', '0.0695', '0.02585', '0.0079', '-0.01529', '-0.0217', '0.03195', '0.0222', '-0.01675', '-0.0384', '0.02403', '-0.04465', '-0.04678', '-0.01103', '0.0492', '0.01431', '-0.03287', '0.02686', '-0.003904', '0.002028', '0.04865', '0.06088', '-0.02446', '0.06006', '-0.04422', '0.00415', '0.010826', '-0.0487', '0.00393', '0.02626', '0.001903', '-0.003222', '-0.0325', '-0.01688', '0.000718', '0.00506', '-0.01516', '0.0536', '-0.01648', '0.03558', '-0.00827', '0.0432', '0.0635', '0.012825', '-0.00882', '0.05762', '-0.01764', '0.01958', '0.1153', '0.01117', '0.0589', '-0.05606', '0.02135', '0.03497']",,,,,,,
mondo:0060562,"encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities","['encephalopathy, neonatal severe, with lactic acidosis and brain abnormalities', 'NELABA', 'lipoyltransferase 2 deficiency']",,617668,,C4540052,,,,,,,,
mondo:0060564,HELIX syndrome,"['HELIX syndrome', 'HELIX', 'hypohidrosis, electrolyte imbalance, lacrimal gland dysfunction, ichthyosis, and xerostomia', 'hypohidrosis-electrolyte imbalance-lacrimal gland dysfunction-ichthyosis-xerostomia syndrome']",,617671,528105,C4522164,,,,,,,,
mondo:0060568,Pilarowski-Bjornsson syndrome,"['PILBOS', 'developmental delay and speech apraxia with or without seizures', 'Pilarowski-Bjornsson syndrome']",,617682,529965,C4540131,,,,,,,,
mondo:0060577,"neurodevelopmental disorder with microcephaly, ataxia, and seizures","['neurodevelopmental disorder with microcephaly, ataxia, and seizures', 'NEDMAS']",,617709,,C4540188,"['-0.0662', '0.10785', '-0.01095', '-0.0682', '-0.01625', '-0.1301', '0.03384', '0.1718', '-0.168', '-0.03903', '-0.0557', '-0.0699', '-0.01361', '-0.000833', '0.03836', '-0.10785', '0.02193', '-0.05453', '-0.07947', '-0.2103', '0.04282', '-0.07074', '-0.009735', '-0.06335', '0.0564', '-0.0936', '0.00485', '-0.0304', '0.03084', '-0.06128', '0.02365', '-0.02133', '0.1631', '0.05017', '-0.01094', '-0.00528', '-0.0511', '-0.04745', '-0.06805', '-0.0901', '0.0539', '-0.09985', '0.02869', '-0.00765', '-0.00669', '-0.1781', '-0.02481', '0.095', '-0.03314', '0.06464', '-0.0823', '0.04187', '-0.0173', '0.02786', '-0.001728', '-0.011185', '0.1046', '-0.02026', '-0.1337', '0.02702', '0.0607', '0.0551', '0.05157', '0.0772', '-0.06192', '0.010735', '0.11035', '0.04828', '-0.1111', '0.136', '-0.0817', '0.0766', '0.01753', '-0.0815', '0.000311', '0.05273', '0.0863', '-0.091', '-0.04453', '-0.01654', '0.01184', '0.03647', '-0.10126', '0.1048', '0.0233', '-0.003521', '-0.007675', '0.095', '0.11224', '0.05997', '0.0444', '0.1489', '0.0087', '0.0315', '0.2004', '0.1006', '0.0793', '-0.0949', '0.04422', '0.05878']",,,,,,,
mondo:0060578,"neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures","['NEMMLAS', 'neurodevelopmental disorder, mitochondrial, with abnormal movements and lactic acidosis, with or without seizures']",,617710,572798,C4540192,"['-0.1213', '0.1794', '0.04495', '-0.04053', '0.004356', '-0.1614', '0.03503', '0.2316', '-0.1575', '0.00368', '-0.05887', '-0.1484', '0.0308', '0.001278', '-0.02853', '-0.01863', '0.0325', '-0.11505', '-0.1333', '-0.3362', '-0.001702', '-0.09045', '0.0861', '-0.02235', '0.0976', '-0.10095', '-0.0367', '0.02129', '0.00529', '-0.06464', '0.01701', '0.02618', '0.2135', '0.0851', '-0.02078', '-0.04672', '-0.1068', '-0.04718', '-0.05325', '-0.1102', '0.04822', '-0.1512', '-0.006325', '0.04453', '-0.02846', '-0.1665', '-0.0649', '0.1236', '-0.00881', '0.1534', '-0.1704', '0.01359', '0.03452', '-0.01607', '0.04703', '-0.05988', '0.10406', '-0.0858', '-0.1577', '0.03592', '0.0738', '0.0556', '0.1465', '-0.00622', '-0.1396', '-0.00222', '0.2046', '0.1105', '-0.1437', '0.1705', '-0.04324', '0.07184', '0.03033', '-0.0679', '0.005966', '0.08093', '0.0868', '-0.01172', '-0.10657', '0.02405', '0.03503', '0.0164', '-0.00486', '0.1148', '0.04428', '0.0184', '0.0298', '0.1722', '0.1747', '0.10516', '0.07837', '0.1691', '-0.001054', '0.08356', '0.2056', '0.186', '0.10144', '-0.11676', '0.02629', '0.0754']",,,,,,,
mondo:0060582,auditory neuropathy-optic atrophy syndrome,"['auditory neuropathy and optic atrophy', 'ANOA']",,617717,542585,C4521678,"['-0.02261', '0.05496', '0.00888', '-0.02324', '-0.006832', '-0.0691', '0.02321', '0.0908', '-0.065', '-0.0231', '-0.02359', '-0.0448', '-0.03976', '-0.01086', '-0.03506', '-0.03076', '-0.00792', '-0.03174', '-0.02818', '-0.0944', '-0.002613', '-0.02686', '0.02328', '0.00986', '0.03217', '-0.00622', '-0.01968', '-0.003382', '-0.008026', '-0.04745', '0.04532', '-0.015396', '0.0759', '0.01357', '0.03308', '-0.01843', '-0.006165', '-0.03177', '-0.02234', '-0.07983', '0.0222', '-0.0747', '0.01607', '-0.0351', '-0.014366', '-0.06683', '-0.02917', '0.02342', '6.497e-05', '0.02441', '-0.022', '0.01889', '0.02081', '-3.165e-05', '-0.02425', '-0.0009604', '0.06204', '-0.02077', '-0.0892', '-0.00239', '0.02356', '0.03162', '0.001589', '0.03882', '-0.03802', '0.003653', '0.0807', '0.05573', '-0.0399', '0.0833', '-0.05008', '0.0227', '0.014496', '-0.04788', '0.03079', '0.01869', '0.02782', '-0.003963', '-0.03458', '-0.04083', '0.03528', '-0.01242', '-0.002672', '0.07275', '-0.02623', '0.0118', '0.007023', '0.0675', '0.0458', '0.02386', '0.01778', '0.07007', '0.02261', '0.0287', '0.1096', '0.01593', '0.06525', '-0.0574', '-0.002506', '0.03354']",,,,,,,
mondo:0060583,platelet abnormalities with eosinophilia and immune-mediated inflammatory disease,"['PLTEID', 'platelet abnormalities with eosinophilia and immune-mediated inflammatory disease', 'immunodeficiency 71 with inflammatory disease and congenital thrombocytopenia']",0112004,617718,,C4540232,"['-0.03244', '0.0334', '0.02084', '-0.02577', '0.0181', '-0.04034', '0.01368', '0.05585', '-0.0322', '-0.02477', '-0.00812', '-0.007153', '-0.000442', '0.01339', '-0.0294', '-0.03824', '-0.00405', '-0.014465', '-0.02113', '-0.0869', '-0.002855', '-0.0204', '0.0476', '-0.013176', '0.0178', '-0.01517', '0.0079', '-0.0002754', '-0.01303', '-0.02255', '0.04105', '-0.0025', '0.05975', '0.02896', '0.03278', '-0.02272', '-0.02899', '-0.02808', '-0.005123', '-0.04736', '0.00423', '-0.05246', '0.02481', '-0.010155', '-0.006763', '-0.04507', '-0.0223', '0.03314', '0.01772', '0.03192', '-0.00819', '0.004375', '0.02437', '0.01013', '-0.02682', '-0.003918', '0.04852', '-0.03473', '-0.07294', '0.00834', '0.0238', '0.03595', '-0.014496', '-0.0063', '0.005745', '0.004837', '0.06287', '0.0504', '-0.04443', '0.06006', '-0.04858', '-0.00813', '0.01093', '-0.015366', '0.02513', '0.01582', '0.01675', '0.0002342', '-0.02754', '-0.03424', '-0.02057', '-0.01461', '-0.0064', '0.0369', '-0.02641', '0.002918', '0.008385', '0.04095', '0.0658', '0.000742', '0.02464', '0.03677', '0.001574', '0.01936', '0.09424', '0.04843', '0.03384', '-0.0539', '-0.000739', '0.010704']",,,,,,,
mondo:0060585,"neuronopathy, distal hereditary motor, type 9","['neuropathy, distal hereditary motor, type 9', 'neuronopathy, distal hereditary motor, type IX', 'HMN9']",0111212,617721,,C4540265,,,,,,,,
mondo:0060589,"facial palsy, congenital, with ptosis and velopharyngeal dysfunction","['facial palsy, congenitla, with ptosis and velopharyngeal dysfunction', 'FPVEPD', 'facial palsy, congenital, with ptosis and velopharyngeal dysfunction']",,617732,,C4540277,"['-0.0942', '0.0891', '0.10443', '-0.1193', '0.0305', '-0.09155', '0.0666', '0.1256', '-0.1458', '-0.1048', '-0.01326', '-0.04742', '0.01785', '0.02312', '-0.0891', '-0.06744', '0.00805', '-0.1026', '-0.0956', '-0.2296', '0.02206', '-0.04794', '0.083', '0.01324', '0.0505', '-0.05847', '-0.01962', '-0.02577', '0.04605', '-0.02747', '0.0754', '0.04074', '0.178', '0.0633', '0.005928', '-0.034', '-0.02869', '-0.0788', '-0.0812', '-0.1389', '0.05148', '-0.1351', '0.005318', '0.010345', '0.001884', '-0.0905', '-0.01104', '0.11255', '0.01055', '0.0471', '-0.06665', '0.04953', '-0.03918', '-0.0352', '-0.04257', '-0.09814', '0.11304', '-0.0758', '-0.1254', '0.071', '0.0917', '0.0564', '-0.04575', '0.05762', '-0.0478', '-0.01778', '0.1188', '0.09515', '-0.1193', '0.1934', '-0.1251', '0.0597', '0.08026', '-0.06137', '0.02577', '0.02382', '0.1108', '-0.05988', '-0.1488', '-0.03778', '0.01851', '-0.0699', '0.019', '0.2261', '-0.0729', '0.02467', '-0.03723', '0.0987', '0.1493', '-0.01283', '0.08185', '0.1049', '0.03503', '0.0742', '0.2354', '0.01566', '0.1316', '-0.11163', '0.0478', '0.10986']",,,,,,,
mondo:0060591,"immunodeficiency, developmental delay, and hypohomocysteinemia","['IMDDHH', 'immunodeficiency, developmental delay, and hypohomocysteinemia']",,617744,,C4540293,"['-0.039', '0.0574', '0.02876', '-0.03796', '0.0119', '-0.0653', '0.03552', '0.08575', '-0.0736', '-0.05035', '-0.01802', '-0.02307', '-0.004658', '0.003586', '-0.007523', '-0.02078', '-0.01137', '-0.03204', '-0.04907', '-0.1349', '-0.001551', '-0.0287', '0.05444', '-0.0399', '0.02849', '-0.0358', '-0.009094', '-0.004616', '0.00352', '-0.0538', '0.04785', '0.0149', '0.1063', '0.03111', '0.0187', '0.001066', '-0.03415', '-0.02632', '-0.04114', '-0.07745', '0.03305', '-0.04572', '0.00912', '-0.00983', '-0.013176', '-0.05865', '-0.02596', '0.03555', '0.01997', '0.03687', '-0.03998', '-0.00874', '0.01058', '0.01072', '-0.014824', '-0.01292', '0.04245', '-0.03198', '-0.0654', '0.0144', '0.02042', '0.02646', '0.00741', '0.01265', '0.005135', '0.0008526', '0.04797', '0.065', '-0.0682', '0.0573', '-0.06744', '0.01718', '0.004253', '-0.0322', '0.02924', '0.03372', '0.02867', '-0.0135', '-0.02005', '-0.01724', '0.02318', '0.0003366', '-0.02429', '0.07367', '-0.007473', '0.01996', '0.03165', '0.07086', '0.0945', '0.03854', '0.03842', '0.07996', '-0.012726', '-0.003983', '0.1337', '0.05518', '0.0711', '-0.07794', '0.01103', '0.0348']",,,,,,,
mondo:0060592,Sweeney-Cox syndrome,"['SWCOS', 'Sweeney-Cox syndrome']",0080538,617746,,C4540299,,,,,,,,
mondo:0060596,neurodevelopmental disorder with dysmorphic facies and distal limb anomalies,"['NEDDFL', 'neurodevelopmental disorder with dysmorphic facies and distal limb anomalies']",,617755,528084,C4540327,"['-0.0464', '0.03577', '0.0295', '-0.04047', '0.00818', '-0.0716', '0.00858', '0.0827', '-0.06445', '-0.03577', '-0.02153', '-0.00827', '0.00925', '0.00402', '-0.02325', '-0.01188', '-0.003199', '-0.03177', '-0.03616', '-0.119', '0.01071', '-0.01872', '0.06573', '-0.0114', '0.0288', '-0.002073', '-0.002974', '-0.01075', '0.02644', '-0.04672', '0.04004', '-0.00709', '0.0633', '0.02986', '0.0222', '-0.03787', '-0.02715', '-0.03937', '-0.013695', '-0.05527', '0.0408', '-0.0767', '0.003626', '-0.01337', '0.014465', '-0.05753', '-0.02245', '0.0564', '-0.007774', '0.02687', '-0.02477', '0.00479', '-0.003489', '0.0021', '-0.02737', '-0.0361', '0.02809', '-0.04288', '-0.06168', '-0.004032', '0.04178', '0.01023', '-0.003513', '0.02766', '0.001112', '0.000616', '0.0657', '0.0589', '-0.05997', '0.0713', '-0.06885', '-0.000481', '0.02742', '-0.02109', '0.0287', '0.0334', '0.02695', '-0.0244', '-0.05072', '-0.0491', '0.000168', '0.00328', '-0.00936', '0.07733', '-0.01464', '0.009674', '0.002562', '0.0469', '0.05933', '-0.00305', '0.02985', '0.04892', '0.003748', '0.02863', '0.1039', '0.02364', '0.07855', '-0.0632', '0.012375', '0.0399']",,,,,,,
mondo:0060611,combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia,"['CIMAH', 'methylenetetrahydrofolate dehydrogenase 1 deficiency', 'combined immunodeficiency and megaloblastic anemia with or without hyperhomocysteinemia']",,617780,,C4540434,"['-0.0641', '0.06635', '0.01974', '-0.02942', '0.03436', '-0.0762', '-0.001804', '0.0693', '-0.0522', '-0.02618', '-0.04745', '-0.03363', '-0.00357', '0.01341', '-0.01261', '-0.06683', '-0.005997', '-0.05765', '-0.0675', '-0.1461', '0.003584', '-0.07043', '0.0715', '-0.02293', '0.02759', '-0.02756', '0.01619', '-0.003471', '-0.00518', '-0.0674', '0.0346', '0.01185', '0.0872', '0.05743', '-0.005024', '-0.02444', '-0.0825', '-0.0498', '-0.05283', '-0.0825', '0.00731', '-0.0891', '0.04797', '-0.02711', '-0.0319', '-0.09326', '-0.017', '0.03815', '0.001533', '0.03534', '-0.02986', '-0.01569', '0.05692', '0.03079', '-0.02655', '-0.01888', '0.04852', '-0.04474', '-0.1077', '0.03705', '0.04813', '0.04214', '0.02687', '-0.004154', '0.02104', '-0.01285', '0.0797', '0.0807', '-0.0775', '0.11694', '-0.04993', '-0.011856', '-0.003891', '-0.0671', '0.02945', '0.03183', '0.02655', '-0.01833', '-0.002823', '-0.029', '0.02043', '-0.02214', '-0.013115', '0.05548', '0.01912', '0.01175', '0.02167', '0.0853', '0.1307', '0.01627', '0.05133', '0.05652', '-0.01727', '-0.002966', '0.1582', '0.1024', '0.05753', '-0.1106', '-0.002121', '0.05115']",,,,,,,
mondo:0060621,"neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy","['neurodevelopmental disorder with microcephaly, seizures, and cortical atrophy', 'NDMSCA']",,617802,,C4540493,,,,,,,,
mondo:0060622,neurodevelopmental disorder with severe motor impairment and absent language,"['NEDMIAL', 'neurodevelopmental disorder with severe motor impairment and absent language', 'neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome']",,617804,647788,C4540496,"['-0.00637', '0.0178', '0.01229', '-0.00896', '0.0001751', '-0.00768', '0.00833', '0.01933', '-0.001801', '0.002226', '0.001492', '-0.003096', '0.004814', '0.001618', '-0.00423', '-0.01524', '-0.001718', '-0.004864', '0.00134', '-0.02647', '0.001244', '-0.006985', '0.006756', '-0.00965', '0.00201', '-0.00811', '0.007282', '0.00537', '-0.00628', '0.0008035', '0.00827', '0.002148', '0.006973', '0.003511', '0.011024', '0.001929', '-0.001984', '-0.004486', '-0.0008073', '-0.012245', '0.002024', '-0.0164', '0.001048', '-0.004948', '0.0005', '-0.01888', '0.00539', '0.00464', '-0.00464', '0.01064', '-0.006832', '-0.00362', '-0.006676', '-0.00932', '0.0009456', '0.006584', '-0.002274', '0.001606', '-0.01868', '-0.005653', '0.00966', '0.006054', '-0.001135', '-0.00496', '0.001855', '0.00927', '0.00504', '0.00935', '-0.01448', '0.00715', '-0.002691', '0.001633', '-0.00688', '-0.003681', '0.001637', '0.00512', '0.006546', '-0.00935', '-0.000524', '-0.014984', '0.009094', '-0.004425', '-0.00962', '0.004337', '-0.006214', '-0.004772', '-0.002039', '-0.000788', '0.01752', '-0.00214', '0.01017', '0.01825', '-0.00954', '0.002737', '0.0188', '0.012726', '0.0002599', '-0.01997', '-0.001839', '0.00657']",,,,,,,
mondo:0060624,"neurodevelopmental disorder with ataxic gait, absent speech, and decreased cortical white matter","['NDAGSCW', 'neurodevelopmental disorder with ataxic GAIT, absent speech, and decreased cortical WHITE matter']",,617807,,C4540498,"['-0.0526', '0.05505', '0.0142', '-0.02063', '0.002596', '-0.0605', '-0.0043', '0.09424', '-0.0791', '-0.0287', '-0.05316', '-0.01469', '0.002445', '0.01218', '0.01226', '-0.02898', '0.01238', '-0.03873', '-0.0345', '-0.137', '0.004345', '-0.03162', '0.04547', '-0.02655', '0.0391', '-0.0388', '-0.000572', '-0.0009217', '-0.003511', '-0.04752', '0.03177', '-0.002024', '0.0924', '0.02245', '0.000594', '-0.0178', '-0.0442', '-0.01459', '-0.00325', '-0.08093', '0.05832', '-0.0815', '-0.011566', '0.010155', '0.005207', '-0.07135', '-0.01416', '0.05942', '0.03925', '0.02026', '-0.01486', '0.001435', '-0.02167', '-0.00549', '-0.02127', '-0.01811', '0.06744', '-0.0677', '-0.05984', '0.0010195', '0.02003', '0.047', '0.03433', '0.0179', '-0.03867', '0.010506', '0.09265', '0.08435', '-0.06415', '0.10004', '-0.04062', '0.03075', '-0.004818', '-0.04877', '0.03265', '0.03918', '0.0349', '0.001189', '-0.0344', '-0.0359', '-0.002829', '-0.02484', '0.01768', '0.09564', '-0.02576', '0.02919', '0.00753', '0.0587', '0.0908', '0.0307', '0.02939', '0.0864', '-0.005825', '0.05643', '0.1393', '0.03973', '0.0651', '-0.0783', '0.015015', '0.05234']",,,,,,,
mondo:0060627,glycosylphosphatidylinositol biosynthesis defect 15,"['developmental delay, epilepsy, cerebellar atrophy, and osteopenia', 'glycosylphosphatidylinositol biosynthesis defect 15', 'GPIBD15']",,617810,529665,C4540520,"['-0.08704', '0.0382', '0.00652', '-0.01438', '0.05215', '-0.0884', '-0.003527', '0.0886', '-0.0595', '-0.01917', '-0.014366', '-0.01015', '0.006023', '0.00748', '-0.0224', '-0.0582', '0.00471', '-0.02618', '-0.04846', '-0.10535', '0.002901', '-0.01424', '0.0777', '-0.0253', '0.036', '-0.03024', '0.02498', '-0.01552', '0.003822', '-0.007183', '0.04868', '0.006737', '0.0886', '0.05405', '0.003555', '-0.05804', '0.01967', '-0.01538', '-0.000562', '-0.054', '0.04556', '-0.0775', '0.00739', '-0.03717', '-0.04083', '-0.0862', '0.00389', '0.02911', '0.01921', '0.0571', '-0.01654', '-0.0537', '-0.01811', '0.04785', '-0.0562', '-0.04807', '0.1001', '-0.00891', '-0.0736', '0.01776', '0.0545', '0.05484', '0.01982', '0.02931', '-0.01593', '-0.002316', '0.0948', '0.05936', '-0.0716', '0.05185', '-0.04935', '0.03986', '0.007607', '-0.03394', '0.03912', '0.0746', '0.0189', '-0.0173', '-0.05466', '-0.0367', '0.0114', '0.002197', '0.00776', '0.0593', '-0.01061', '-0.004757', '0.03973', '0.0794', '0.0678', '-0.001452', '0.04453', '0.06027', '-0.02159', '0.003777', '0.1338', '0.03903', '0.09247', '-0.1458', '-0.01135', '0.015366']",,,,,,,
mondo:0060629,"neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive","['NDHMSR', 'neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal recessive']",,617820,,CN737161,,,,,,,,
mondo:0060631,Alkuraya-Kucinskas syndrome,"['ALKKUCS', 'Alkuraya-Kucinskas syndrome']",0111555,617822,610569,CN737163,"['-0.00763', '0.03912', '-0.0005302', '-0.01697', '0.02594', '-0.03952', '0.012344', '0.05197', '-0.03134', '-0.03177', '-0.006317', '-0.007164', '-8.816e-05', '0.007507', '-0.01892', '-0.01938', '-0.00987', '0.00488', '-0.013275', '-0.05615', '0.001972', '-0.002403', '0.01837', '-0.02896', '0.02647', '0.002337', '-0.01233', '-0.009834', '0.01427', '-0.02107', '0.03635', '-0.01536', '0.05792', '0.01678', '0.01348', '-0.0104', '-0.00491', '-0.02966', '-0.0005364', '-0.03026', '0.01036', '-0.03577', '0.001465', '-0.02422', '0.01241', '-0.042', '-0.01878', '0.0331', '0.02141', '0.01512', '-0.005756', '0.00874', '-0.001637', '-0.01392', '-0.0265', '-0.008934', '0.0312', '-0.01403', '-0.02736', '-0.0101', '0.02867', '0.005386', '0.01581', '0.01516', '0.008705', '-0.003742', '0.0355', '0.01862', '-0.03964', '0.0571', '-0.02026', '0.006943', '0.00054', '-0.017', '0.02354', '0.01285', '-0.006424', '-0.00965', '-0.02742', '-0.0184', '0.0184', '0.001723', '-0.02498', '0.04727', '0.004578', '-0.004612', '0.02104', '0.03644', '0.03992', '0.004635', '0.0328', '0.03314', '0.010704', '0.01958', '0.07367', '0.01137', '0.02101', '-0.0587', '-0.02657', '0.02238']",,,,,,,
mondo:0060640,"neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy","['neurodevelopmental disorder with microcephaly, epilepsy, and brain atrophy', 'NEDMEBA']",,617862,,CN787271,"['-0.03967', '0.0771', '0.00997', '-0.04434', '0.01904', '-0.0831', '0.01591', '0.09534', '-0.0805', '-0.04007', '-0.03146', '-0.02777', '-0.01144', '0.001157', '-0.004642', '-0.0477', '0.007328', '-0.03001', '-0.056', '-0.1288', '0.00966', '-0.0329', '0.0431', '-0.01894', '0.01391', '-0.03952', '-0.011116', '-0.000453', '-0.013855', '-0.03372', '0.03494', '-0.01451', '0.0893', '0.03099', '0.01362', '0.005875', '-0.012596', '-0.02011', '-0.01642', '-0.05536', '0.02826', '-0.0697', '0.01188', '-0.012856', '-0.01471', '-0.07947', '-0.01732', '0.0579', '-0.01877', '0.0186', '-0.006657', '0.005814', '-0.01718', '0.005314', '-0.0249', '-0.01035', '0.05838', '-0.02295', '-0.0769', '0.02283', '0.03418', '0.01213', '0.01373', '0.02429', '-0.0252', '0.0187', '0.0691', '0.04773', '-0.07214', '0.0811', '-0.04727', '0.02701', '0.0274', '-0.0394', '0.01124', '0.0384', '0.02615', '-0.0235', '-0.02917', '-0.03882', '-0.004562', '0.012436', '-0.02197', '0.0759', '-0.005905', '-0.00999', '0.006855', '0.05963', '0.0783', '0.01622', '0.02942', '0.0737', '0.00873', '0.0204', '0.0971', '0.03214', '0.0733', '-0.0531', '0.01323', '0.02661']",,,,,,,
mondo:0060641,neurodevelopmental disorder with or without seizures and gait abnormalities,"['NEDSGA', 'neurodevelopmental disorder with or without seizures and gait abnormalities']",,617864,,CN800195,"['-0.06174', '0.08655', '0.0464', '-0.04755', '0.01631', '-0.11096', '0.011635', '0.133', '-0.12134', '-0.02492', '-0.0416', '-0.04443', '-0.001873', '0.0145', '-0.02582', '-0.04816', '0.01526', '-0.0682', '-0.05957', '-0.1907', '-0.00891', '-0.0292', '0.0771', '-0.02725', '0.0546', '-0.05164', '0.00721', '-0.03041', '0.02768', '-0.06866', '0.0513', '-0.0355', '0.10126', '0.05466', '0.01131', '-0.02568', '-0.05948', '-0.04865', '-0.01884', '-0.09015', '0.0472', '-0.0988', '0.03287', '0.01519', '0.01447', '-0.08405', '-0.04272', '0.07086', '-0.01576', '0.06775', '-0.04803', '0.04858', '0.014366', '-0.0003533', '0.005257', '-0.0286', '0.06604', '-0.05618', '-0.11847', '0.0335', '0.0468', '0.0437', '0.0261', '0.01938', '-0.05145', '0.01556', '0.1206', '0.05954', '-0.0797', '0.094', '-0.06635', '0.03735', '0.01782', '-0.05936', '0.0323', '0.0404', '0.04547', '-0.02048', '-0.0655', '-0.047', '0.01316', '-0.002596', '-0.01845', '0.1246', '0.004986', '0.02682', '-0.007202', '0.1037', '0.121', '0.0403', '0.02164', '0.1255', '0.00966', '0.05984', '0.1632', '0.0739', '0.105', '-0.0953', '0.00838', '0.04477']",,,,,,,
mondo:0060642,"neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features","['neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features', 'NEDMAGA']",,617865,,CN800196,"['-0.02023', '0.0327', '0.013535', '-0.01434', '0.00794', '-0.04703', '0.0115', '0.0552', '-0.04126', '-0.02286', '-0.01898', '-0.002117', '-0.01044', '0.007378', '-0.01837', '-0.00662', '0.00813', '-0.02571', '-0.0287', '-0.0648', '-3.68e-05', '-0.003683', '0.02493', '-0.01677', '0.0266', '-0.001191', '0.0003386', '-0.007015', '-0.000928', '-0.01917', '0.02621', '-0.001221', '0.0387', '0.0174', '0.003174', '-0.012505', '-0.01023', '-0.008064', '-0.00947', '-0.0464', '0.02911', '-0.02917', '0.002378', '-0.003944', '0.004837', '-0.04', '-0.0002261', '0.01653', '0.00772', '0.02995', '-0.02423', '-0.00145', '-0.00949', '0.0001736', '-0.003418', '-0.01683', '0.03056', '-0.02017', '-0.03394', '0.00855', '0.0184', '0.02092', '1.63e-05', '0.01767', '-0.0132', '0.01077', '0.03732', '0.03165', '-0.0327', '0.0406', '-0.03192', '0.0194', '0.01459', '-0.02036', '0.014496', '0.01791', '0.01339', '-0.001', '-0.013695', '-0.02324', '0.00831', '-0.006695', '-0.001663', '0.02684', '-0.01034', '0.001942', '-0.0003562', '0.02705', '0.04913', '0.01004', '0.01152', '0.03876', '0.0007052', '0.012856', '0.0639', '0.01634', '0.0341', '-0.0465', '-0.00657', '0.02515']",,,,,,,
mondo:0060650,Leber congenital amaurosis with early-onset deafness,"['LCAEOD', 'Leber congenital amaurosis with early-onset deafness']",0112240,617879,,CN807950,,,,,,,,
mondo:0060659,neurodevelopmental disorder with poor language and loss of hand skills,"['NDPLHS', 'neurodevelopmental disorder with poor language and loss of hand skills']",,617903,,,,,,,,,,
mondo:0060662,Diamond-Blackfan anemia-like,"['DBAL', 'Diamond-Blackfan anemia-like']",,617911,,CN873436,,,,,,,,
mondo:0060663,"congenital heart defects, multiple types, 5","['CHTD5', 'CONGENITAL heart defects, multiple types, 5']",,617912,,CN873437,"['-0.0082', '0.01976', '-0.0001773', '-0.01341', '0.0254', '-0.02234', '0.004475', '0.02454', '-0.02078', '-0.01327', '-0.006012', '-0.0153', '0.00116', '0.009766', '-0.011154', '-0.02075', '-0.006107', '-0.00874', '-0.02203', '-0.04514', '0.000569', '0.001152', '0.02272', '-0.010315', '0.00356', '-0.01372', '-0.01042', '-0.01366', '-0.005005', '-0.01208', '0.03745', '-0.012955', '0.0335', '0.005157', '0.01216', '-0.00829', '-0.0104', '0.001744', '0.000715', '-0.03177', '0.00851', '-0.02145', '0.01429', '-0.0003965', '0.0006747', '-0.02432', '-0.013596', '0.02982', '0.00998', '0.01421', '-0.002464', '-0.00621', '0.01033', '-0.01143', '-0.01807', '-0.01625', '0.0203', '0.003145', '-0.02235', '0.00118', '0.01134', '0.00497', '-0.001274', '-0.002007', '-0.00338', '0.01186', '0.034', '0.01927', '-0.01697', '0.02798', '-0.004654', '0.001398', '-0.006405', '-0.0301', '0.00979', '0.01379', '0.001673', '-0.00387', '-0.02167', '-0.02386', '-0.000711', '0.007507', '-0.007156', '0.02739', '-0.00658', '-0.007538', '0.015434', '0.01552', '0.0346', '-0.003868', '-0.00027', '0.03143', '0.00363', '-0.0002952', '0.06274', '0.022', '0.01619', '-0.03177', '-0.007133', '0.00812']",,,,,,,
mondo:0060664,"neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities","['NEDMCR', 'neurodevelopmental disorder with microcephaly, cataracts, and renal abnormalities']",0081263,617913,,CN889218,"['-0.06186', '0.0643', '0.03394', '-0.0602', '0.00862', '-0.10583', '0.007626', '0.17', '-0.12476', '-0.04553', '-0.03662', '-0.0337', '-0.01327', '0.03044', '-0.066', '-0.0665', '0.01964', '-0.03558', '-0.0651', '-0.1971', '-0.006546', '-0.03497', '0.0656', '-0.03082', '0.04086', '-0.0606', '-0.003864', '-0.00761', '0.04608', '-0.05035', '0.0678', '-0.01246', '0.1422', '0.06137', '0.02585', '-0.02145', '-0.04074', '-0.0734', '-0.0328', '-0.0764', '0.061', '-0.075', '0.0363', '-0.01784', '-0.004513', '-0.10876', '-0.02629', '0.0949', '-0.01347', '0.07513', '-0.0396', '0.0215', '-0.002321', '-0.014404', '-0.028', '-0.03204', '0.06616', '-0.04828', '-0.1483', '0.02415', '0.07153', '0.00746', '0.01071', '0.02037', '0.00456', '0.01683', '0.11945', '0.09357', '-0.09924', '0.12305', '-0.11816', '0.03525', '0.0275', '-0.03333', '0.04962', '0.03445', '0.05988', '-0.04355', '-0.0676', '-0.0353', '0.01627', '0.02177', '-0.02332', '0.11664', '-0.009926', '0.003244', '0.03915', '0.09076', '0.1506', '0.0653', '0.0379', '0.1193', '-0.01176', '0.0316', '0.1755', '0.07263', '0.1148', '-0.10706', '0.03537', '0.04858']",,,,,,,
mondo:0060666,"hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome","['hypotonia, ataxia, developmental delay, and tooth enamel defect syndrome', 'HADDTS']",,617915,,CN895589,"['-0.02827', '0.02863', '0.013245', '-0.0217', '0.0144', '-0.051', '-0.008316', '0.0755', '-0.03906', '-0.01979', '-0.03055', '-0.0257', '-0.01356', '0.02284', '-0.0232', '-0.03592', '0.001075', '-0.02121', '-0.02542', '-0.096', '-0.002468', '-0.00881', '0.0324', '-0.02332', '0.03014', '-0.02182', '-0.01321', '-0.001911', '0.01203', '-0.04056', '0.03113', '0.0004063', '0.0481', '0.01892', '-0.001296', '-0.005344', '-0.01859', '-0.01057', '-0.01967', '-0.04755', '0.00884', '-0.04758', '0.0015335', '0.002123', '-0.01979', '-0.03564', '-0.003866', '0.0243', '0.01046', '0.01965', '-0.02858', '0.007633', '-0.001403', '-0.003967', '-0.013664', '-0.02454', '0.0347', '-0.01907', '-0.06366', '0.014885', '0.02861', '0.01088', '-0.001543', '0.01584', '-0.002016', '0.00406', '0.06158', '0.0459', '-0.03778', '0.0565', '-0.05255', '0.01616', '0.009735', '-0.0419', '0.02258', '0.00977', '0.02713', '-0.01752', '-0.02415', '-0.02342', '-0.005543', '-0.005898', '-0.02028', '0.03558', '-0.005077', '0.0003946', '0.00662', '0.03247', '0.07056', '0.00993', '0.009415', '0.05627', '0.001316', '0.012825', '0.07446', '0.03568', '0.0386', '-0.0637', '0.02547', '0.01729']",,,,,,,
mondo:0060670,"amyotrophic lateral sclerosis, susceptibility to, 25","['ALS25', 'amyotrophic lateral sclerosis, susceptibility to, 25']",,617921,,CN895594,,,,,,,,
mondo:0060671,"epilepsy, juvenile myoclonic, susceptibility to, 10","['epilepsy, juvenile myoclonic, susceptibility to, 10', 'EJM10']",0111325,617924,,,,,,,,,,
mondo:0060677,chromosome 1p35 deletion syndrome,['chromosome 1p35 deletion syndrome'],,617930,,CN244562,,,,,,,,
mondo:0060688,"hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency","['hyperthyroxinemia, euthyroid, due to decreased peripheral conversion of T4', 'hyperthyroxinemia, euthyroid, caused by generalized 5-prime-deiodinase deficiency']",,617953,,CN244571,,,,,,,,
mondo:0060690,phenytoin toxicity,"['phenytoin toxicity', 'foetal hydantoin syndrome', 'arene oxide detoxification defect', 'diphenylhydantoin, defect in hydroxylation of', 'fetal hydantoin syndrome']",,617955,,,,,,,,,,
mondo:0060702,"spondyloepimetaphyseal dysplasia, di rocco type","['SEMDDR', 'spondyloepimetaphyseal dysplasia, Di Rocco type']",,617974,,CN244923,"['-0.01825', '0.05362', '0.02415', '-0.01429', '0.03912', '-0.0744', '6.85e-06', '0.0658', '-0.0779', '-0.0204', '-0.02583', '-0.01846', '-0.005527', '0.006184', '-0.02005', '-0.01991', '0.0246', '-0.02603', '-0.01217', '-0.1035', '-0.00971', '-0.01218', '0.0714', '-0.000605', '8.446e-05', '-0.00429', '-0.01906', '-0.03152', '0.00856', '-0.042', '0.03717', '-0.005035', '0.04358', '0.0322', '0.03177', '-0.02872', '-0.00511', '-0.04147', '-0.007675', '-0.06003', '0.00955', '-0.0754', '0.001158', '0.000932', '-0.03056', '-0.0544', '-0.01221', '0.0698', '0.01599', '-0.01218', '-0.002876', '-0.01035', '0.02122', '-0.01263', '-0.03035', '-0.05252', '0.01311', '-0.0494', '-0.07745', '0.0123', '0.03214', '0.00888', '-0.01811', '0.01144', '-0.01235', '-0.0004537', '0.059', '0.02943', '-0.05536', '0.05005', '-0.05566', '-0.0002149', '0.02185', '-0.06384', '0.01475', '0.02979', '-0.02322', '0.00439', '-0.04132', '-0.03168', '-0.01217', '0.012375', '-0.02649', '0.0627', '-0.02422', '0.02809', '0.001997', '0.05743', '0.05664', '0.01294', '0.01205', '0.04062', '0.01636', '0.0291', '0.1327', '0.02841', '0.0729', '-0.0733', '0.0233', '0.0424']",,,,,,,
mondo:0060704,neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures,"['Elhattab-Alkuraya syndrome', 'NEDSBAS', 'neurodevelopmental disorder with spastic quadriplegia and brain abnormalities with or without seizures']",,617977,,CN244929,"['-0.03928', '0.1454', '0.04614', '-0.0956', '0.01581', '-0.1263', '0.005733', '0.1469', '-0.1908', '-0.02771', '-0.06616', '-0.0805', '0.00973', '-0.00987', '0.02664', '-0.0944', '0.03192', '-0.1014', '-0.1079', '-0.252', '-0.0051', '-0.0587', '0.07587', '-0.02518', '0.0776', '-0.0885', '0.02258', '-0.007267', '0.02489', '-0.06824', '0.01993', '-0.04175', '0.1833', '0.0602', '-0.001094', '-0.02583', '-0.0668', '-0.0821', '-0.03644', '-0.1206', '0.0489', '-0.1522', '0.01968', '0.01723', '0.00829', '-0.13', '-0.0563', '0.08044', '-0.05264', '0.0853', '-0.05658', '0.071', '-0.01999', '0.01505', '0.003899', '-0.00335', '0.1083', '-0.04153', '-0.1744', '0.07367', '0.05457', '0.062', '0.0853', '0.0375', '-0.1133', '0.0253', '0.1797', '0.0864', '-0.156', '0.167', '-0.1385', '0.081', '0.014725', '-0.10834', '0.0688', '0.0698', '0.08685', '-0.03348', '-0.0805', '-0.06052', '0.02155', '0.01936', '-0.02039', '0.1997', '-0.0008063', '0.01318', '-0.02094', '0.1534', '0.1398', '0.06128', '0.03876', '0.1643', '0.02528', '0.0901', '0.1816', '0.0948', '0.11884', '-0.133', '0.0221', '0.06396']",,,,,,,
mondo:0060707,Ververi-Brady syndrome,"['VERBRAS', 'Ververi-Brady syndrome']",,617982,580940,CN244927,"['-0.00905', '0.01184', '0.00532', '0.00841', '0.004803', '-0.02199', '0.004402', '0.02596', '-0.01779', '-0.014656', '-0.01439', '0.002298', '0.0007796', '0.01591', '-0.002834', '-0.00544', '-0.01428', '0.000656', '-0.01015', '-0.0297', '0.001263', '-0.01471', '0.01984', '-0.00555', '-0.006203', '-0.003967', '-0.01331', '-0.01677', '0.00072', '-0.02129', '0.007477', '-0.004578', '0.01365', '0.01616', '0.001017', '-0.004158', '-0.002708', '-0.006767', '0.0001678', '-0.02', '-0.001063', '-0.01567', '-0.00464', '-0.001699', '0.002245', '-0.02527', '-0.007416', '0.01672', '-0.00587', '0.004402', '-0.004726', '-0.004528', '3.54e-05', '-0.00972', '-0.010826', '-0.011086', '0.01082', '-0.00648', '-0.02188', '0.002596', '0.01234', '0.005108', '0.000321', '0.008026', '-0.009155', '0.001719', '0.024', '0.001279', '-0.01826', '0.02321', '-0.02257', '0.01189', '0.007835', '-0.01492', '0.009636', '0.008224', '-0.00809', '-0.007122', '-0.00637', '0.002422', '0.000535', '0.003633', '-0.004086', '0.01183', '0.001096', '-0.005733', '0.01648', '0.00851', '0.01727', '0.01006', '0.003643', '0.01545', '-0.0006456', '0.01111', '0.03995', '0.007755', '0.01651', '-0.0207', '-0.008354', '0.005848']",,,,,,,
mondo:0060711,Jaberi-Elahi syndrome,"['Jaberi-Elahi syndrome', 'JABELS']",,617988,,CN244943,"['-0.005432', '0.00936', '-0.003525', '0.0048', '-0.005238', '-0.01303', '0.003605', '0.009674', '0.004246', '0.004963', '0.002117', '0.003817', '-0.00821', '-0.003181', '-0.00521', '0.003416', '0.002306', '-0.004402', '0.00461', '-0.01772', '-0.007244', '-0.01288', '-0.001366', '-0.00891', '-0.001324', '-0.0105', '-0.005047', '-0.00194', '-0.0001863', '-0.01044', '0.002686', '-0.00754', '0.000699', '0.003504', '0.001543', '0.004658', '-0.006638', '0.003172', '-0.00877', '0.0001782', '0.006958', '0.001238', '-0.004135', '-0.003893', '0.001918', '-0.00569', '-0.002108', '0.0009685', '0.00403', '0.003147', '0.00648', '-0.00714', '0.000988', '0.00803', '-0.0001943', '-0.01106', '0.01207', '-0.004215', '-0.00449', '0.001537', '-0.0007033', '0.011024', '-0.004635', '-0.004055', '-0.00758', '0.002783', '-0.001364', '0.0142', '-0.00877', '0.01391', '-0.009926', '0.003904', '0.00964', '-0.01054', '0.00866', '0.001796', '-0.007786', '-0.003492', '-0.01113', '-0.001813', '0.0001609', '0.00767', '-0.00307', '-0.001633', '0.00821', '0.002264', '0.001608', '0.013214', '0.00965', '-0.002611', '-0.005753', '0.01581', '-0.000994', '0.008965', '0.01851', '-0.003351', '0.01281', '-0.007378', '-0.000505', '-0.0001854']",,,,,,,
mondo:0060713,"deafness, congenital heart defects, and posterior embryotoxon","['deafnes, congenital heart defects, and posterior embryotoxon', 'DCHE']",,617992,,,"['-0.10126', '0.04434', '0.0916', '-0.0543', '0.113', '-0.09015', '0.03247', '0.147', '-0.1113', '-0.0775', '-0.07513', '-0.0699', '-0.0003917', '0.0302', '-0.1901', '-0.0943', '-0.03705', '-0.07196', '-0.05338', '-0.209', '0.016', '-0.00624', '0.05002', '-0.003004', '0.05136', '-0.02718', '-0.02968', '0.003714', '0.1216', '-0.02133', '0.1061', '0.01116', '0.1126', '0.0641', '0.03787', '-0.07556', '0.02184', '-0.01938', '0.00654', '-0.1677', '0.07434', '-0.0837', '0.06354', '-0.02719', '-0.0347', '-0.1032', '-0.02959', '0.152', '0.01197', '0.07837', '-0.01942', '-0.013275', '0.0594', '-0.05954', '-0.0884', '-0.07574', '0.1674', '-0.00010145', '-0.1603', '0.01529', '0.0343', '0.0292', '-0.0712', '0.03934', '-0.0685', '-0.00926', '0.1635', '0.1621', '-0.1671', '0.1307', '-0.0843', '0.04117', '0.06064', '-0.1255', '0.02858', '-0.011894', '0.05475', '-0.083', '-0.10754', '-0.06042', '-0.00493', '-0.00969', '-0.013794', '0.1532', '-0.04028', '-0.01317', '0.03702', '0.10144', '0.0673', '0.0436', '0.06964', '0.1255', '0.087', '0.0752', '0.293', '0.0022', '0.1906', '-0.1559', '-0.0216', '0.05643']",,,C566604,,,,
mondo:0060714,"tumoral calcinosis, hyperphosphatemic, familial, 2","['tumoral calcinosis, hyperphosphatemic, familial, 2', 'HFTC2']",,617993,,,,,,,,,,
mondo:0060715,"tumoral calcinosis, hyperphosphatemic, familial, 3","['HFTC3', 'tumoral calcinosis, hyperphosphatemic, familial, 3']",,617994,,,,,,,,,,
mondo:0060720,congenital disorder of glycosylation with defective fucosylation,"['CDGF', 'congenital disorder of glycosylation with defective fucosylation']",,,,CN248517,"['-0.1059', '0.0551', '0.04645', '-0.01232', '0.0917', '-0.12317', '-0.01656', '0.0958', '-0.10175', '-0.05096', '-0.013664', '-0.03735', '0.02968', '0.001325', '-0.0427', '-0.01903', '0.0147', '-0.0765', '-0.0725', '-0.2205', '-0.01335', '-0.02655', '0.11', '-0.0281', '0.03943', '-0.006577', '-0.0355', '-0.06683', '0.07227', '-0.0561', '0.0618', '0.02719', '0.1144', '0.07544', '-0.005547', '-0.01836', '-0.03772', '-0.02551', '-0.0445', '-0.1218', '0.0329', '-0.1186', '-0.0105', '-0.04343', '-0.03406', '-0.0949', '-0.01534', '0.09064', '0.0888', '0.05402', '-0.03564', '-0.0162', '0.03021', '0.006474', '-0.05905', '-0.0765', '0.0888', '0.0154', '-0.1322', '0.03302', '0.05972', '0.04288', '0.02861', '0.03522', '-0.01343', '-0.008514', '0.08386', '0.07733', '-0.1277', '0.06238', '-0.0735', '0.02946', '0.005733', '-0.03418', '0.0736', '0.0661', '0.0461', '-0.002913', '-0.08105', '-0.03745', '0.007263', '-0.05298', '-0.02007', '0.09515', '-0.01755', '0.007507', '0.0378', '0.0651', '0.1071', '0.011116', '0.0003345', '0.11066', '-0.005344', '0.0368', '0.1608', '0.0714', '0.123', '-0.1556', '0.01522', '0.0708']",,,,,,,
mondo:0060724,glycosylphosphatidylinositol biosynthesis defect 17,"['glycosylphosphatidylinositol biosynthesis defect 17', 'GPIBD17']",,618010,,CN248527,"['-0.1356', '0.04892', '0.01663', '-0.03214', '0.06665', '-0.12317', '-0.00269', '0.08673', '-0.0637', '-0.0654', '-0.01245', '-0.0138', '0.0277', '0.002823', '-0.0258', '-0.0293', '0.02876', '-0.0331', '-0.0402', '-0.1755', '0.001415', '-0.01359', '0.09576', '-0.03754', '0.02312', '-0.03665', '0.006245', '-0.01059', '0.0215', '-0.0696', '0.0627', '0.0725', '0.1205', '0.05246', '0.01746', '-0.09235', '0.03156', '0.00754', '-0.03024', '-0.1026', '0.05914', '-0.10645', '-0.02892', '-0.03763', '-0.05136', '-0.11444', '-0.00744', '0.0698', '0.0363', '0.03275', '-0.01852', '-0.07794', '-0.03757', '0.03357', '-0.0945', '-0.07916', '0.11005', '-0.0328', '-0.098', '0.03207', '0.04382', '0.07306', '0.05383', '0.005947', '0.0076', '-0.003725', '0.11395', '0.05008', '-0.1185', '0.0684', '-0.07324', '0.06165', '0.01374', '-0.02333', '0.0653', '0.09174', '0.02513', '-0.011696', '-0.05795', '0.01003', '0.03506', '0.011955', '0.0158', '0.05823', '-0.01343', '-0.02734', '0.06415', '0.0969', '0.0772', '0.01464', '0.0489', '0.081', '-0.00903', '-0.0012245', '0.1993', '0.0678', '0.0947', '-0.1818', '-0.02492', '0.01174']",,,,,,,
mondo:0060729,"protoporphyria, erythropoietic, 2","['EPP2', 'protoporphyria, erythropoietic, 2']",,618015,,CN248523,"['-0.0315', '0.0758', '-0.02043', '-0.01904', '0.03247', '-0.07275', '-0.01143', '0.0393', '-0.04858', '0.002594', '-0.0733', '0.02054', '0.019', '0.01022', '-0.04028', '-0.02347', '-0.02336', '0.00962', '-0.01136', '-0.128', '-0.01762', '-0.04242', '0.11365', '-0.03546', '0.03156', '-0.02707', '-0.005165', '-0.05273', '-0.003126', '-0.08105', '0.05466', '-0.01736', '0.0729', '0.03217', '0.03043', '-0.047', '-0.04263', '-0.01624', '-0.01653', '-0.0763', '0.02261', '-0.082', '0.08044', '-0.04257', '-0.0192', '-0.09186', '-0.02953', '0.0381', '0.02917', '0.03357', '-0.003925', '-0.0222', '0.01387', '0.0447', '-0.0703', '-0.01971', '0.0711', '-0.0394', '-0.11414', '-0.001118', '0.0567', '0.0241', '0.02753', '0.01262', '-0.003426', '0.002525', '0.07654', '0.0508', '-0.06247', '0.05838', '-0.04807', '-0.01724', '0.01752', '-0.0596', '0.06046', '0.0153', '-0.02629', '-0.006348', '-0.05203', '-0.06885', '0.01881', '-0.01627', '-0.02127', '0.04108', '-0.0168', '0.01176', '0.04324', '0.10364', '0.0741', '-0.01643', '0.05908', '0.05692', '-0.0124', '0.003395', '0.1271', '0.05276', '0.05777', '-0.1256', '-0.02446', '-0.001318']",,,,,,,
mondo:0060732,tetraamelia syndrome 2,"['TETAMS2', 'tetraamelia syndrome 2', 'tetraamelia syndrome 2 with pulmonary agenesis']",0112193,618021,,,,,,,,,,
mondo:0060733,humerofemoral hypoplasia with radiotibial ray deficiency,"['humerofemoral hypoplasia with radiotibial ray deficiency', 'HHRRD', 'Hfhrtrd']",,618022,,CN248526,"['-0.0584', '0.04956', '0.02904', '-0.03125', '0.06757', '-0.05075', '0.02185', '0.10754', '-0.0961', '-0.0961', '-0.0261', '-0.04996', '-0.02606', '-0.01793', '-0.05054', '-0.05862', '0.01628', '-0.04745', '-0.0699', '-0.1877', '-0.01721', '-0.04105', '0.1011', '-0.01587', '0.05606', '-0.013885', '-0.0279', '-0.0193', '0.0596', '-0.074', '0.04456', '0.02254', '0.12396', '0.04614', '0.05', '-0.04715', '0.013504', '-0.04376', '-0.02974', '-0.08844', '0.0341', '-0.07806', '0.05426', '-0.03207', '-0.039', '-0.11414', '0.03125', '0.09143', '0.0196', '0.04776', '-0.02736', '-0.0734', '0.01165', '-0.001447', '-0.1059', '-0.05743', '0.07135', '-0.06836', '-0.1434', '-0.00941', '0.0678', '0.04205', '0.00762', '0.01855', '-0.00875', '-0.01472', '0.0992', '0.11664', '-0.1001', '0.1372', '-0.0809', '0.04092', '0.04086', '-0.1047', '0.0484', '0.02502', '0.0813', '-0.073', '-0.0911', '-0.05963', '0.00457', '0.01346', '-0.00671', '0.12415', '0.01071', '-0.004852', '0.01023', '0.1042', '0.12396', '-0.001598', '0.00648', '0.09265', '0.0282', '0.01321', '0.2203', '0.0319', '0.1287', '-0.1427', '0.03424', '0.06537']",,,,,,,
mondo:0060745,intellectual developmental disorder with or without epilepsy or cerebellar ataxia,"['IDDECA', 'intellectual developmental disorder with or without epilepsy or cerebellar ataxia']",,618060,,CN252646,"['-0.0482', '0.0726', '-0.06207', '-0.0994', '0.03323', '-0.2162', '0.03973', '0.2', '-0.2046', '-0.0891', '-0.1239', '-0.0572', '-0.0388', '-0.0484', '0.0961', '-0.1738', '0.02264', '-0.1185', '-0.1046', '-0.2847', '0.04626', '-0.014626', '-0.007034', '-0.09735', '0.03397', '-0.117', '0.02861', '-0.04977', '0.05908', '-0.04575', '0.03723', '-0.02206', '0.1937', '0.04617', '-0.005524', '-0.01553', '-0.1343', '-0.1046', '-0.1577', '-0.128', '0.08344', '-0.149', '0.03018', '0.04703', '-0.03192', '-0.2141', '-0.014206', '0.1158', '-0.0318', '-0.00566', '-0.02414', '0.0888', '-0.01807', '-0.02081', '0.003881', '0.01401', '0.1355', '-0.0615', '-0.194', '0.03815', '0.05582', '0.0466', '0.06976', '0.0745', '-0.12134', '0.0328', '0.1209', '0.1306', '-0.1268', '0.1716', '-0.0592', '0.0906', '0.01143', '-0.1433', '0.0006967', '0.0642', '0.1268', '-0.07635', '-0.05737', '-0.000663', '-0.04486', '0.0234', '-0.10767', '0.1565', '0.01365', '-0.00809', '-0.02777', '0.1774', '0.1858', '0.0875', '0.0354', '0.2056', '-0.0567', '0.00719', '0.2534', '0.09326', '0.11346', '-0.12006', '0.0712', '0.1743']",,,,,,,
mondo:0060752,neurodevelopmental disorder with spasticity and poor growth,"['neurodevelopmental disorder with spasticity and poor growth', 'NEDSG']",0070421,618076,,,"['-0.05725', '0.0861', '0.0429', '-0.05777', '0.02711', '-0.1236', '0.03714', '0.1268', '-0.1142', '-0.04288', '-0.04083', '-0.02429', '0.001875', '0.011826', '-0.01573', '-0.0342', '0.02303', '-0.0429', '-0.0706', '-0.1975', '0.02235', '-0.04825', '0.054', '-0.04315', '0.0313', '-0.02176', '0.0005355', '-0.03354', '-0.00976', '-0.05103', '0.07153', '0.03433', '0.1167', '0.04376', '0.000663', '-0.001281', '-0.03732', '-0.03156', '-0.03433', '-0.0646', '0.0497', '-0.0873', '0.002508', '0.00384', '-0.004192', '-0.10583', '-0.01866', '0.04956', '0.0133', '0.05493', '-0.06836', '0.000822', '0.000953', '0.015076', '-0.014496', '-0.03065', '0.05988', '-0.0337', '-0.119', '0.05206', '0.010635', '0.03293', '0.02281', '0.0239', '-0.001321', '0.01269', '0.1018', '0.06107', '-0.0958', '0.1123', '-0.0959', '0.0329', '0.0134', '-0.06525', '0.0492', '0.05887', '0.03708', '-0.03047', '-0.0387', '-0.0416', '-0.00704', '-0.01663', '-0.02861', '0.12024', '0.00897', '0.03854', '0.03296', '0.04703', '0.12494', '0.0435', '0.02457', '0.11554', '-0.01012', '0.02792', '0.1384', '0.07477', '0.0786', '-0.08887', '0.01817', '0.0428']",,,,,,,
mondo:0060758,"spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits","['SCA42ND', 'spinocerebellar ataxia 42, early-onset, severe, with neurodevelopmental deficits']",,618087,,,"['-0.06934', '0.0898', '0.001532', '-0.08276', '-0.06537', '-0.1678', '0.00439', '0.1715', '-0.2012', '-0.039', '-0.0535', '-0.05228', '-0.03564', '-0.02904', '0.08563', '-0.1124', '0.0008373', '-0.03796', '-0.04605', '-0.1925', '-0.01328', '-0.0723', '0.00736', '-0.05798', '0.0523', '-0.0194', '-0.00523', '-0.07947', '0.02411', '-0.07336', '0.005276', '0.03473', '0.2045', '0.0783', '-0.003859', '-0.09125', '-0.09326', '-0.07404', '-0.1299', '-0.1005', '0.04034', '-0.1473', '0.007343', '0.001572', '-0.03818', '-0.1931', '-0.09204', '0.08307', '0.01074', '-0.01607', '-0.0489', '0.09735', '-0.06445', '-0.0274', '0.01323', '-0.07837', '0.135', '-0.0844', '-0.1705', '0.04895', '0.06476', '0.03577', '0.0351', '0.07355', '-0.0782', '-0.00874', '0.1432', '0.04422', '-0.089', '0.1951', '-0.03308', '0.0637', '0.00835', '-0.125', '0.09485', '0.05606', '0.06027', '-0.0232', '-0.0425', '0.01688', '-0.00759', '-0.0088', '-0.05325', '0.1244', '0.06033', '0.02371', '0.010445', '0.1426', '0.1641', '0.05893', '0.08014', '0.1462', '-0.008644', '0.0334', '0.2311', '0.1257', '0.11993', '-0.0521', '0.05582', '0.07495']",,,,,,,
mondo:0060759,"neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures","['NEDAMSS', 'IRF2BPL-related regressive neurodevelopmental disorder-dystonia-seizures syndrome', 'neurodevelopmental disorder with regression, abnormal movements, loss of speech, and seizures']",0081327,618088,597623,,"['-0.0995', '0.1935', '0.1594', '-0.11505', '0.02129', '-0.1665', '0.0845', '0.1954', '-0.1748', '-0.02065', '-0.1153', '-0.09875', '-0.00615', '0.01404', '0.02254', '-0.02061', '0.0628', '-0.0973', '-0.06', '-0.307', '0.01297', '-0.11395', '0.03342', '-0.0491', '0.1312', '-0.1021', '-0.02946', '0.01822', '-0.0383', '-0.0758', '0.01643', '0.02173', '0.1907', '0.07184', '0.03522', '-0.03014', '-0.04172', '-0.06714', '-0.06726', '-0.1587', '0.0788', '-0.1078', '-0.01747', '0.01304', '0.0357', '-0.1704', '-0.04016', '0.10187', '-0.01942', '0.1915', '-0.1376', '0.0907', '-0.01581', '0.02199', '0.045', '-0.04944', '0.0674', '-0.06033', '-0.158', '-0.0257', '0.03796', '0.06714', '0.05896', '0.02502', '-0.0784', '-0.03748', '0.2368', '0.0647', '-0.1451', '0.1353', '-0.0678', '0.109', '-0.04236', '-0.1113', '0.02463', '0.05157', '0.12164', '-0.03397', '-0.1678', '-0.03543', '-0.01016', '-0.0006', '-0.01005', '0.2001', '0.005222', '-0.01502', '0.01717', '0.1516', '0.1664', '0.1594', '0.02502', '0.2441', '-0.01399', '0.1283', '0.2407', '0.15', '0.0804', '-0.1334', '0.149', '0.1046']",,,,,,,
mondo:0060760,intellectual developmental disorder with dysmorphic facies and behavioral abnormalities,"['INTELLECTUAL developmental disorder with DYSMORPHIC facies and behavioural abnormalities', 'IDDFBA', 'INTELLECTUAL developmental disorder with DYSMORPHIC facies and behavioral abnormalities']",,618089,,,"['-0.03165', '0.05692', '0.02092', '-0.0408', '0.01855', '-0.0618', '0.00997', '0.0948', '-0.06046', '-0.03973', '-0.0334', '-0.01817', '0.003496', '-0.005688', '-0.02875', '-0.01973', '0.00784', '-0.02646', '-0.0469', '-0.1192', '0.00692', '-0.012596', '0.04572', '-0.02985', '0.0298', '-0.01438', '-0.02005', '-0.01536', '0.01169', '-0.04495', '0.04346', '-0.00997', '0.0861', '0.02228', '0.01295', '-0.01354', '-0.03091', '-0.0342', '-0.01356', '-0.04697', '0.02718', '-0.06006', '0.003412', '-0.00947', '0.01411', '-0.05786', '-0.006878', '0.04343', '0.009995', '0.01575', '-0.0422', '0.003584', '-0.002728', '-0.0082', '-0.0006595', '-0.013855', '0.0292', '-0.0383', '-0.06003', '0.02422', '0.02162', '0.0206', '-0.011246', '0.00407', '-7.075e-05', '0.002764', '0.05066', '0.0768', '-0.05258', '0.06213', '-0.06384', '0.011185', '0.01756', '-0.01578', '0.01202', '0.01903', '0.0365', '-0.01209', '-0.05365', '-0.0469', '0.00629', '-0.01779', '-0.02513', '0.0757', '0.007072', '0.02036', '-0.001692', '0.0642', '0.08185', '0.02837', '0.0155', '0.06476', '-2.78e-05', '0.01622', '0.10974', '0.04022', '0.05386', '-0.06305', '0.03543', '0.0275']",,,,,,,
mondo:0060761,neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum,"['neurodevelopmental disorder with epilepsy and hypoplasia of the corpus callosum', 'NEDEHCC']",,618090,,,"['-0.09015', '0.1311', '0.0516', '-0.1465', '0.0008903', '-0.1349', '0.00719', '0.2174', '-0.1776', '-0.1146', '-0.0941', '-0.1169', '-0.03458', '-0.074', '-0.03238', '-0.09717', '0.01866', '-0.05658', '-0.06915', '-0.2299', '0.05423', '-0.0355', '0.1015', '-0.0756', '0.0548', '-0.06183', '0.01938', '0.02109', '0.0915', '-0.1301', '0.06134', '-0.011955', '0.1816', '0.01953', '0.0367', '-0.01634', '-0.06067', '-0.1083', '-0.07227', '-0.10126', '0.10486', '-0.132', '0.01355', '-0.02425', '-0.03714', '-0.176', '-0.00903', '0.06836', '-0.02805', '0.05112', '-0.02827', '0.03967', '-0.07294', '-0.00442', '-0.0899', '0.007607', '0.07086', '-0.07776', '-0.152', '0.04465', '-0.00214', '0.01903', '0.0661', '0.06238', '-0.0488', '0.01791', '0.1351', '0.1322', '-0.1321', '0.1525', '-0.0827', '0.0964', '0.0116', '-0.0467', '-0.003017', '0.04443', '0.1186', '-0.0796', '-0.122', '-0.0711', '-0.003056', '0.0409', '-0.03925', '0.205', '0.00897', '-0.02678', '-0.01131', '0.1754', '0.133', '0.01404', '0.01103', '0.1829', '-0.0003371', '0.021', '0.2495', '0.02571', '0.1807', '-0.132', '0.1043', '0.1359']",,,,,,,
mondo:0060763,"intellectual developmental disorder with speech delay, dysmorphic facies, and t-cell abnormalities","['intellectual developmental disorder with dysmorphic facies, speech delay, and t-cell abnormalities', 'INTELLECTUAL developmental disorder with speech delay, DYSMORPHIC facies, and T-cell abnormalities', 'IDDSFTA', 'BCL11B-related BAFopathy']",,618092,,,"['-0.0796', '0.09796', '0.07874', '-0.09656', '0.03143', '-0.1185', '0.03442', '0.1691', '-0.1387', '-0.07556', '-0.0539', '-0.0272', '0.02443', '-0.01379', '-0.03452', '0.00983', '0.02766', '-0.04962', '-0.0821', '-0.2247', '0.013214', '-0.01735', '0.082', '-0.04755', '0.0683', '-0.05603', '-0.005585', '-0.009544', '0.02812', '-0.0825', '0.076', '-0.01365', '0.1682', '0.0603', '0.0518', '-0.03427', '-0.05658', '-0.06903', '-0.04022', '-0.125', '0.0574', '-0.0913', '-0.02083', '0.002449', '-0.00966', '-0.0891', '-0.01627', '0.077', '-0.01985', '0.03488', '-0.09595', '0.00858', '-0.002672', '0.00741', '-0.01868', '-0.02261', '0.02971', '-0.0565', '-0.1025', '0.03174', '0.02711', '0.0257', '-0.00567', '0.03653', '0.0096', '-0.01271', '0.09784', '0.1421', '-0.11365', '0.1333', '-0.10675', '0.03793', '0.02394', '-0.06012', '0.008545', '0.0421', '0.08453', '-0.0448', '-0.0824', '-0.0468', '0.03363', '-0.01843', '-0.03687', '0.154', '-0.0292', '0.028', '-0.006874', '0.1356', '0.1656', '0.08734', '0.06696', '0.1626', '0.00763', '0.0447', '0.2181', '0.0813', '0.0872', '-0.1305', '0.0786', '0.0783']",,,,,,,
mondo:0060764,tetraamelia syndrome 1,"['tetraamelia syndrome 1', 'tetraamelia syndrome, autosomal recessive', 'TETAMS1', 'Tetra-amelia syndrome 1']",0112192,273395,,,,,,,,,,
mondo:0060765,fibroepithelial polyp,"['fibroepithelial polyp', 'fibropapilloma, benign']",,,,,,C3337,,,,,,
mondo:0060766,anal polyp,"['polyp of anus', 'polyp of the anus', 'anal polyp']",,,,C0267573,,C3957,,,,,,
mondo:0060768,gingival fibroepithelial polyp,"['fibroepithelial polyp of the gum', 'fibroepithelial polyp of the gingiva', 'gum fibroepithelial polyp', 'gingival fibroepithelial polyp', 'fibroepithelial polyp of gingiva', 'fibroepithelial polyp of gum']",,,,C0399441,,C4693,,,,,,
mondo:0060774,vaginal fibroepithelial polyp,"['fibroepithelial polyp of the vagina', 'fibroepithelial polyp of vagina', 'vaginal fibroepithelial stromal polyp', 'vaginal fibroepithelial polyp']",,,,C0750071,,C4948,,,,,,
mondo:0060777,cervical fibroepithelial polyp,"['uterine cervix fibroepithelial polyp', 'Cervical fibroepithelial polyp']",,,,C1516413,,C40200,,,,,,
mondo:0060778,adult Fanconi syndrome,"['adult Fanconi^s syndrome', 'adult Fanconi syndrome']",,,,,,C4377,,,,,,
mondo:0060779,acquired Fanconi syndrome,['acquired Fanconi syndrome'],,,,C0341702,,C78296,,,,,,
mondo:0060781,Preeyasombat-Varavithya syndrome,['Fanconi syndrome caused by degraded tetracycline'],,,,C2930859,,,,C535269,,,,
mondo:0060782,premalignant hematological system disease,['premalignant hematologic condition'],,,,C1335471,,C27274,,,,,,
mondo:0060783,classic congenital adrenal hyperplasia,['classic congenital adrenal hyperplasia'],,,,C4329672,,C131423,,,,,,
mondo:0100000,MED12-related intellectual disability syndrome,['MED12 X-linked syndromic intellectual disability'],,,,,,,,,,,,
mondo:0100001,alpha-gal syndrome,"['red meat allergy', 'alpha-gal allergy', 'allergic galactose-alpha-1,3-galactose disease', 'tick bite meat allergy', 'AGS']",,,,,,,,,,,,
mondo:0100002,food protein-induced allergic proctocolitis,"['FPIPC', 'milk protein proctocololitis', 'allergic proctocolitis']",,,,,,,,,,,,
mondo:0100003,susceptibility to angioedema induced by ACE inhibitors,"['angioedema induced by ACE inhibitors, susceptibility to']",,300909,,,,,,,,,,
mondo:0100004,mast cell activation syndrome,"['mast cell activation disease', 'disorder of mast cell activation', 'MACS']",,,,,,,,D000090267,,,,
mondo:0100005,primary mast cell activation syndrome,,,,,,,,,,,,,
mondo:0100006,secondary mast cell activation syndrome,,,,,,,,,,,,,
mondo:0100008,food protein-induced enterocolitis syndrome,['FPIES'],,,,,,,,,,,,
mondo:0100009,"structural congenital heart disease, multiple types - GATA4",,,,,,,,,,,,,
mondo:0100010,tendinopathy,"['disease of tendon', 'tendon disease', 'disorder of tendon', 'tendon disease or disorder']",,,,,,,1001434,D052256,,,,
mondo:0100011,tendinosis,,,,,,,,,,,,,
mondo:0100012,paratenonitis,,,,,,,,,,,,,
mondo:0100013,paratenonitis with tendinosis,,,,,,,,,,,,,
mondo:0100014,autoimmune retinopathy,"['retina autoimmune disease', 'AIR', 'autoimmune disease of retina']",,,,C3203657,,,,,,,,
mondo:0100015,adult-onset segmental dystonia,"['an adult-onset, focal or segmental, isolated dystonia that is characterised by cervical or cranial dystonia that often begins in the fourth decade (range 7-54 years).', 'an adult-onset, focal or segmental, isolated dystonia that is characterized by cervical or cranial dystonia that often begins in the fourth decade (range 7-54 years).', 'DYT-GNAL']",,,,,,,,,,,,
mondo:0100016,early-onset generalized dystonia,"['early-onset, generalised dystonia with mild syndromic features', 'early-onset, generalized dystonia with mild syndromic features', 'A generalized isolated dystonia characterized by early-onset, which may be clinically indistinguishable from DYT-TOR1A and may be the most common cause of early-onset generalized dystonia, at least outside the Askenazi Jewish population.', 'A generalised isolated dystonia characterised by early-onset, which may be clinically indistinguishable from DYT-TOR1A and may be the most common cause of early-onset generalised dystonia, at least outside the Askenazi Jewish population.', 'DYT-KMT2B', 'early-onset generalised isolated dystonia']",,,,,,,,,,,,
mondo:0100017,pityriasis rubra pilaris,,9212,,,C0032027,,C85014,,D010916,696.4,L44.0,,
mondo:0100018,adult onset pityriasis rubra pilaris,['adult onset PRP'],,,,,,,,,,,,
mondo:0100019,ECHS1-related paroxysmal dyskinesia,['ECHS1 deficiency-associated paroxysmal exercise-induced dyskinesia'],,,,,,,,,,,,
mondo:0100020,atypical childhood epilepsy with centrotemporal spikes,,,,,,,,,,,,,
mondo:0100021,photosensitive occipital lobe epilepsy,,,,,,,,,,,,,
mondo:0100022,neonatal/infantile epilepsy syndrome,,,,,,,,,,,,,
mondo:0100023,self-limited familial neonatal epilepsy,['self-limited familial and non-familial neonatal seizures'],,,,,,,,,,,,
mondo:0100024,self-limited familial infantile epilepsy,['self-limited familial and non-familial infantile seizures'],,,,,,,,,,,,
mondo:0100025,epilepsy of infancy with migrating focal seizures,,,,,C4518639,,,,,,,,
mondo:0100026,myoclonic encephalopathy in non-progressive disorder,,,,,,,,,,,,,
mondo:0100028,immune epilepsy,,,,,,,,,,,,,
mondo:0100029,antibody mediated epilepsy,,,,,,,,,,,,,
mondo:0100030,adolescent/adult-onset epilepsy syndrome,,,,,,,,,,,,,
mondo:0100031,adolescent/adult onset autosomal dominant epilepsy with auditory features,,,,,,,,,,,,,
mondo:0100032,familial temporal lobe epilepsy syndrome,,,,,,,,,,,,,
mondo:0100033,metabolic epilepsy,,,,,,,,,,,,,
mondo:0100034,cerebral folate deficiency,,,,,,,,,,,,,
mondo:0100035,structural epilepsy,,,,,,,,,,,,,
mondo:0100036,variable age onset epilepsy,['variable age at onset electroclinical syndrome'],0050706,,,,,,,,,,,
mondo:0100037,juvenile onset pityriasis rubra pilaris,['juvenile onset PRP'],,,,,,,,,,,,
mondo:0100038,complex neurodevelopmental disorder,,,,,,,,,,,,,
mondo:0100039,CDKL5 disorder,"['inherited genetic disease caused by mutation in CDKL5', 'CDKL5', 'CDKL5 inherited genetic disease', 'CDKL5-related disorder']",,,,,,,,,,,,
mondo:0100040,FOXG1 disorder,['FOXG1 inherited genetic disease'],,,,,,,,,,,,
mondo:0100041,secondary trimethylaminuria,,,,,,,,,,,,,
mondo:0100042,cardiac conduction defect,"['conduction disorder', 'cardiac conduction disorder', 'disorder of cardiac conduction', 'heart conduction disorder']",,115080,871,,,C78245,,,,,,
mondo:0100043,"epidermodysplasia verruciformis, susceptibility to",,,,,,,,,,,,,
mondo:0100044,acrofrontofacionasal dysostosis 1,"['acrofrontofacionasal dysostosis 1', 'AFFN dysostosis 1', 'acrofrontofacionasal dysostosis type 1']",,201180,,C4551987,,,,C538186,,,,
mondo:0100045,"epidermodysplasia verruciformis, susceptibility to, 1","['EV1', 'epidermodysplasia verruciformis 1']",,226400,,,,,,,,,,
mondo:0100046,"exfoliation syndrome, susceptibility to","['pseudoexfoliation of the lens', 'pseudoexfoliation glaucoma', 'pseudoexfoliation syndrome']",,177650,,,,,,,,,,
mondo:0100047,"basal cell carcinoma, susceptibility to",,,,,,,,,,,,,
mondo:0100048,"graft-versus-host disease, susceptibility to",['GVHDS'],,614395,,,,,,,,,,
mondo:0100049,"narcolepsy, susceptibility to",,,,,,,,,,,,,
mondo:0100050,"Usher syndrome, type 1D/F","['Usher syndrome, type 1D/F, CDH23/PCDH15, digenic', 'USH1D/F, CDH23/PCDH15, digenic']",,,,,,,,,,,,
mondo:0100051,idiopathic mast cell activation syndrome,,,,,,,,,,,,,
mondo:0100052,acetazolamide-responsive hereditary episodic ataxia,,,,,,,,,,,,,
mondo:0100053,anaphylaxis,['systemic anaphylaxis'],,,,,,C107101,,D000707,,,10002198,
mondo:0100054,idiopathic anaphylaxis,,,,,,,,,,,,,
mondo:0100055,intraosseous spindle cell rhabdomyosarcoma with TFCP2/NCOA2 rearrangements,"['intraosseous rhabdomyosarcoma with FUS-TFCP2 fusion', 'intraosseous rhabdomyosarcoma defined by FUS-TFCP2 fusion']",,,,,,C178236,,,,,,
mondo:0100056,exercise-induced anaphylaxis,['EIAn'],,,,,,,,,,,,
mondo:0100057,food-dependent exercise-induced anaphylaxis,,,,,,,,,,,,,
mondo:0100058,hypervalinemia and hyperleucine-isoleucinemia,"['branched-chain aminotransferase deficiency', 'hypervalinemia and hyperleucine-isoleucinemia', 'hypervalinemia or hyperleucine-isoleucinemia', 'HVLI']",,618850,,,,,,,,,,
mondo:0100059,hypereosinophilia of undetermined significance,['HEUS'],,,,,,,,,,,,
mondo:0100060,congenital/infantile spindle cell rhabdomyosarcoma with VGLL2/NCOA2/CITED2 rearrangements,,,,,,,C178232,,,,,,
mondo:0100061,PRPS1 deficiency disorder,,,,,,,,,,,,,
mondo:0100062,developmental and epileptic encephalopathy,"['early infantile epileptic encephalopathy', 'early infantile epileptic encephalopathy with suppression-bursts', 'developmental and epileptic encephalopathy', 'Ohtahara syndrome', 'EIEE', 'DEE', 'infantile epileptic encephalopathy', 'infantile spasm', 'early infantile epileptic encephalopathy with burst-suppression', 'epileptic encephalopathy, infantile', 'epileptic encephalopathy, early infantile']",2481,,1934,C0037769,"['0.659', '0.3704', '-0.523', '0.075', '-0.7734', '-0.692', '0.902', '0.5317', '-0.525', '-0.1825', '-0.4287', '-0.4314', '-0.0882', '0.1185', '0.3481', '0.2107', '-0.426', '-0.3423', '-0.1714', '-0.6904', '0.02097', '0.341', '0.776', '-0.7363', '0.232', '-0.0278', '-0.6353', '0.03995', '-0.3418', '-0.0976', '0.331', '-0.0491', '-0.2412', '0.9897', '-0.1388', '0.4172', '0.3025', '-0.4893', '-0.0631', '-0.1785', '0.0466', '-0.5557', '-0.2988', '-0.2063', '0.3604', '0.0817', '-0.1265', '0.3416', '-0.463', '0.847', '-0.2109', '0.0253', '-0.1501', '-0.4863', '0.4688', '-0.1907', '0.1746', '-0.0925', '-0.4985', '0.346', '-0.373', '-0.3997', '0.2544', '0.226', '-0.516', '0.2935', '0.6123', '-0.2378', '-0.3584', '0.4749', '0.2153', '0.2378', '0.05685', '-0.1727', '0.323', '0.727', '0.6504', '-0.267', '-0.6084', '-0.01234', '-0.1527', '0.4138', '-0.1919', '0.06122', '0.305', '-0.07983', '-0.10095', '0.686', '0.451', '0.2466', '0.224', '0.51', '0.0627', '0.1032', '-0.4255', '0.1384', '0.406', '-0.693', '0.475', '0.0662']",C84788,1000643,,345.6,,10071545,
mondo:0100063,Pericytoma with t(7;12),,0080896,,,,,,,,,,,
mondo:0100064,tyrosine hydroxylase deficiency,"['tyrosine 3-monooxygenase deficiency', 'TH deficiency', 'tyrosine Hydroxylase deficiency']",,,,,,C157158,,,,,,
mondo:0100065,TH-deficient infantile parkinsonism and motor delay,,,,,,,,,,,,,
mondo:0100066,TH-deficient progressive infantile encephalopathy,['tyrosine hydroxylase-deficient progressive infantile encephalopathy'],,,,,,,,,,,,
mondo:0100067,childhood spindle cell rhabdomyosarcoma,,,,,,,C123397,,,,,,
mondo:0100068,SLC10A7-congenital disorder of glycosylation,['SLC10A7-CDG'],,,,,,,,,,,,
mondo:0100069,hearing impairment and infertile male syndrome,['HIIMS'],,,,,,,,,,,,
mondo:0100070,neuroendocrine disorder,,,,,,,,,,,,,
mondo:0100071,cardiocutaneous syndrome,,,,,,,,,,,,,
mondo:0100072,"neonatal diabetes, congenital sensorineural hearing loss and congenital cataracts",,,,,,,,,,,,,
mondo:0100073,methicillin-resistant staphylococcus aureus infectious disease,['MRSA'],,,,,,,,,,,,
mondo:0100074,norovirus infectious disease,,,,,,,,,,,,,
mondo:0100075,jaw fracture,,,,,,,,,D007572,,,,
mondo:0100076,juvenile idiopathic scoliosis,,,,459696,,,,,,,,,
mondo:0100077,congenital alveolar dysplasia,['CAD'],,,,,,,,,,,,
mondo:0100078,resistant hypertension,,,,,,,,,,,,,
mondo:0100079,"developmental and epileptic encephalopathy, 6","['DEE6', 'epileptic encephalopathy, early infantile, 6', 'EIEE6', 'Dravet syndrome']",,607208,,,,,,,,,,
mondo:0100080,cardioectodermal syndrome,['cardio-ectodermal syndrome'],,,,,,,,,,,,
mondo:0100081,sleep disorder,"['sleep disturbances', 'parasomnia', 'disturbances, sleep', 'sleep disturbance']",,,,,,C3376,,,,,,
mondo:0100082,LEOPARD syndrome 1,"['LEOPARD syndrome type 1', 'lentiginosis, cardiomyopathic', 'multiple lentigines syndrome', 'LPRD1']",0080548,151100,,,,,,,,,,
mondo:0100083,hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1,"['familial platelet syndrome with predisposition to acute myelogenous leukemia', 'platelet disorder, aspirin-like', 'FPDMM', 'asprin-like platelet disorder', 'FPD/AML syndrome', 'familial platelet syndrome with predisposition to acute myelogenous leukaemia', 'familial thrombocytopenia with propensity to acute myelogenous leukemia', 'thrombocytopenia, familial, with propensity to acute myelogenous leukaemia', 'thrombocytopenia, familial, with propensity to acute myelogenous leukemia', 'FPS/AML syndrome', 'familial platelet disorder with associated myeloid malignancy', 'platelet disorder, familial, with associated myeloid malignancy', 'familial thrombocytopenia with propensity to acute myelogenous leukaemia']",,601399,,,,,,,,,,
mondo:0100084,alpha-actinopathy,,,,,,,,,,,,,
mondo:0100085,cancer of long bone of upper limb,,,,,,,,,,,,,
mondo:0100086,perinatal disease,['perinatal disorder'],,,,,,,,,,P00-P96,,
mondo:0100087,familial Alzheimer disease,"['FAD', 'GARD:0000632', 'Alzheimer disease, familial']",,,,,,,,,,,,
mondo:0100089,GATA1-Related X-Linked Cytopenia,,,,,,,,,,,,,
mondo:0100090,congenital alveolar dysplasia due to FGF10,['CAD due to FGF10'],,,,,,,,,,,,
mondo:0100091,inherited pseudoxanthoma elasticum,"['inherited Gronblad Strandberg syndrome', 'inherited PXE']",,,,,,,,,,,,
mondo:0100092,"myoclonus, familial, 2",['MYOCL2'],,618364,,,,,,,,,,
mondo:0100093,"myoclonus, familial, 1","['FCM', 'MYOCL1', 'myoclonus, familial cortical']",,614937,,,,,,,,,,
mondo:0100094,cannabinoid hyperemesis syndrome,['CHS'],,,,,,,,,,,,
mondo:0100095,"neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures","['neurodegeneration, childhood-onset, stress-induced, with variable ataxia and seizures', 'CONDSIAS']",0070352,618170,,,,,,,,,,
mondo:0100096,COVID-19,"['SARS-coronavirus 2', 'beta-CoV', 'coronavirus disease 2019', 'betacoronavirus', 'β-coronavirus', '2019-nCoV', 'severe acute respiratory syndrome coronavirus 2', 'severe acute respiratory syndrome coronavirus 2 infectious disease', 'β-CoV', 'β-CoVs', '2019 novel coronavirus', 'SARS-CoV-2', 'beta-CoVs', '2019-nCoV infection', '2019 novel coronavirus infection']",0080600,,,,,,,D000086382,,U07.1,,
mondo:0100097,congenital alveolar dysplasia due to TBX4,['CAD due to TBX4'],,,,,,,,,,,,
mondo:0100098,"dystonia, dopa-responsive, with or without hyperphenylalaninemia, autosomal recessive",,,,,,,,,,,,,
mondo:0100099,retrograde cricopharyngeus dysfunction,['R-CPD'],,,,,,,,,,,,
mondo:0100100,SELENON-related myopathy,['SEPN1-related myopathy'],,,,,,,,,,,,
mondo:0100101,fetal akinesia deformation sequence 1,"['Pena-Shokeir syndrome, type 1', 'Pena-Shokeir syndrome type 1', 'FADS1']",0111377,208150,994,,"['-0.544', '0.2325', '-0.2255', '-0.414', '-0.09717', '-0.3003', '0.078', '0.6323', '-0.7925', '-0.6035', '0.003574', '0.02267', '-0.0891', '-0.01596', '-0.215', '0.0884', '0.4768', '0.0763', '-0.1537', '-0.5356', '-0.0342', '0.1461', '0.3806', '-0.03305', '0.4255', '0.3733', '-0.446', '0.3203', '0.691', '-0.226', '-0.0627', '-0.06232', '0.4995', '0.1572', '0.4268', '-0.3145', '0.1305', '0.2358', '0.3816', '0.1924', '-0.3062', '0.1508', '-0.3652', '0.284', '-0.2195', '-0.0848', '0.259', '0.6606', '0.47', '-0.051', '-0.4526', '-0.481', '0.2354', '0.0523', '-0.736', '-0.3965', '0.2686', '-0.2175', '0.3286', '0.5327', '0.3281', '0.2622', '-0.3523', '0.05838', '-0.2866', '-0.1497', '0.08075', '0.2161', '-0.2358', '0.2979', '-0.1301', '0.8516', '0.0928', '-0.11066', '-0.2119', '-0.1573', '0.253', '0.1438', '-0.8115', '0.392', '0.3557', '0.0269', '0.4558', '-0.2808', '-0.3', '-0.409', '0.1703', '0.7085', '0.2617', '0.1151', '0.1903', '-0.1615', '-0.05847', '-0.077', '0.6123', '0.414', '0.18', '-0.55', '0.3267', '0.3157']",,,,,,,
mondo:0100102,fetal akinesia deformation sequence 2,['FADS2'],0111378,618388,,,,,,,,,,
mondo:0100103,fetal akinesia deformation sequence 3,['FADS3'],0111376,618389,,,,,,,,,,
mondo:0100104,fetal akinesia deformation sequence 4,['FADS4'],0111379,618393,,,,,,,,,,
mondo:0100105,brain small vessel disease 3,['BSVD3'],0112315,618360,,,,,,,,,,
mondo:0100107,non-neonatal early infantile epileptic encephalopathy,,,,,,,,,,,,,
mondo:0100108,TPM3-related myopathy,"['autosomal dominant TPM3-related myopathy', 'congenital myopathy related to TPM3', 'TPM3 myopathy']",,,,,,,,,,,,
mondo:0100109,Zinner syndrome,,,,,,,,,,,,,
mondo:0100110,adenovirus renal infection,,,,,,,,,,,,,
mondo:0100111,focal segmental glomerulosclerosis and neurodevelopmental syndrome,['FSGSNEDS'],,619428,,,,,,,,,,
mondo:0100112,acyl-CoA binding domain containing protein 5 deficiency,"['ACBD5 deficiency', 'acyl-CoA binding domain containing protein 5 deficiency']",,,,,,,,,,,,
mondo:0100113,hearing loss with skin disease,,,,,,,,,,,,,
mondo:0100114,dry age related macular degeneration,"['dry AMD', 'dry ARMD']",,,,,,,,,,,10075567,
mondo:0100115,acute flaccid myelitis,['AFM'],0080947,,623801,,,C128379,,C000629404,,,,
mondo:0100116,Middle East respiratory syndrome,"['camel flu', 'MERS']",0080642,,576074,C3694279,,C128424,,,,,,
mondo:0100118,hereditary skin disorder,"['disease, genetic skin', 'genetic skin diseases', 'genetic skin disease', 'diseases, genetic skin', 'skin disease, genetic']",,,,,,,,D012873,,,,
mondo:0100119,Knobloch syndrome 2,,,618458,,,,,,,,,,
mondo:0100120,vector-borne disease,"['vector-borne infection', 'vector-borne infectious disease']",,,,,,,,D000079426,,,,
mondo:0100121,"SCN4A-related myopathy, autosomal recessive",['congenital myopathy with severe foetal hypokinesia'],,,,,,,,,,,,
mondo:0100122,GNPTAB-mucolipidosis,"['GNPTAB-related disorder', 'UDP-N-acetylglucosamine-1-phosphotransferase subunit alpha/beta deficiency']",,,,,,,,,,,,
mondo:0100123,toxic bronchiolitis,,,,,,,,,,,,,
mondo:0100124,NAA10-related syndrome,"['NAA10 X-linked syndromic intellectual disability', 'X-linked syndromic intellectual disability caused by mutation in NAA10', 'NAA10-related syndrome']",,,,,,,,,,,,
mondo:0100125,hallucinogen-persisting perception disorder,['hallucinogen abuse with hallucinogen persisting perception disorder'],,,,,,,,,,F16.183,,
mondo:0100126,P5CS deficiency,['delta1-pyrroline-5-carboxylate synthetase deficiency'],,,,,,,,,,,,
mondo:0100127,toxic bronchiolitis obliterans,,,,,,,,,,,,,
mondo:0100128,coinfection,,,,,C0275524,,,,D060085,,,,
mondo:0100129,intracranial arachoid cyst,"['arachnoid cysts, intracranial', 'intracranial arachnoid cysts']",,207790,,,,,,,,,,
mondo:0100130,adult acute respiratory distress syndrome,"['adult acute respiratory distress syndrome', 'respiratory distress syndrome, adult', 'adult RDS', 'adult respiratory distress syndrome, ARDS', 'ARDS', 'adult ARDS', 'adult respiratory distress syndrome']",11394,,70578,C0035222,,,,D012128,,,,
mondo:0100131,pediatric acute respiratory distress syndrome,['PARDS'],,,,,,,,,,,,
mondo:0100132,intrahepatic bile duct adenosquamous carcinoma,,,,,,,,,,,,,
mondo:0100133,mitochondrial complex I deficiency,"['isolated NADH-CoQ reductase deficiency', 'isolated mitochondrial respiratory chain complex I deficiency', 'NADH coenzyme Q reductase deficiency', 'complex 1 mitochondrial respiratory chain deficiency', 'isolated NADH-ubiquinone reductase deficiency', 'isolated complex I deficiency', 'isolated NADH-coenzyme Q reductase deficiency']",0060536,,2609,C2936907,"['-0.203', '0.3225', '-0.1115', '-0.02156', '-0.008316', '-0.3623', '-0.0426', '-0.1216', '-0.338', '0.51', '-0.03992', '-0.1725', '0.1602', '-0.366', '-0.01973', '-0.134', '-0.1653', '-0.1683', '-0.2177', '-0.5815', '0.10693', '-0.1185', '0.4495', '0.1292', '0.12134', '0.2715', '0.006805', '0.1473', '0.0749', '-0.07', '0.089', '0.215', '0.6304', '0.1985', '0.0361', '-0.503', '-0.2229', '-0.1354', '-0.3926', '-0.26', '0.1433', '-0.5093', '0.255', '0.2119', '-0.01909', '-0.4897', '0.2043', '0.1702', '0.09406', '-0.001329', '-0.1604', '-0.1315', '-0.2203', '-0.1694', '-0.0787', '-0.3552', '0.5713', '0.1561', '-0.2683', '0.324', '-0.00618', '-0.207', '0.588', '0.03738', '-0.5474', '0.2893', '0.1558', '0.567', '-0.2151', '0.57', '-0.4302', '0.04535', '0.2101', '0.326', '0.1925', '0.2344', '0.0458', '0.04794', '-0.1586', '0.2976', '0.262', '0.3103', '-0.5273', '0.1316', '0.2712', '0.11334', '0.4211', '0.3413', '0.3271', '-0.07153', '0.2798', '-0.03604', '0.151', '-0.2043', '0.4993', '0.3599', '0.388', '-0.03165', '-0.1592', '-0.1403']",,,C537475,,,,
mondo:0100134,"mitochondrial complex I deficiency, mitochondrial type",,,,,,,,,,,,,
mondo:0100135,Dravet syndrome,"['Dravet syndrome', 'SME', 'myoclonic epilepsy, severe, of infancy', 'DS']",0080422,,,C0751122,,C116573,,,345.10,,,
mondo:0100137,telomere syndrome,"['short telomere syndrome', 'STS']",,,,,,C152065,,,,,,
mondo:0100138,X-linked recessive mitochondrial myopathy,"['X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features']",,,,,,,,,,,,
mondo:0100144,Uner Tan Syndrome,['recessive quadrupedalism'],,,,,,,,,,,,
mondo:0100146,ATP6AP2-related disorder,,,,,,,,,,,,,
mondo:0100147,SATB2 associated disorder,"['SAS', 'SATB2-associated syndrome']",,,576278,,,,,,,,,
mondo:0100148,X-linked complex neurodevelopmental disorder,,,,,,,,,,,,,
mondo:0100149,PNPLA6-related spastic paraplegia with or without ataxia,,,,,,,,,,,,,
mondo:0100150,RYR1-related myopathy,,,,,,,,,,,,,
mondo:0100151,nephropathic cystinosis,"['cystinosis, atypical nephropathic', 'CTNS', 'Abderhalden-Kaufmann-Lignac syndrome', 'Abderhalden Kaufmann Lignac syndrome', 'cystinosis, nephropathic', 'Abderhalden Lignac Kaufmann disease', 'Abderhalden-Lignac-Kaufmann disease']",,219800,,C2930877,,C129932,,C535335,,,,
mondo:0100152,DKC1-related disorder,,,,,,,,,,,,,
mondo:0100153,tubulinopathy,,0112227,,,,,,,,,,,
mondo:0100154,TUBB3-related tubulinopathy,,,,,,,,,,,,,
mondo:0100155,retinal dystrophy-ataxia-pituitary hormone abnormality-hypogonadism syndrome,['RAPH syndrome'],,,,,,,,,,,,
mondo:0100156,Imerslund-Grasbeck syndrome type 1,"['megaloblastic anemia, 1', 'megaloblastic Anaemia type 1', 'Imerslund-Grasbeck syndrome 1', 'megaloblastic Anemia type 1', 'enterocyte cobalamin malabsorption', 'MGA1', 'Mga1', 'megaloblastic anemia, Finnish type', 'enterocyte intrinsic factor receptor, defect of', 'pernicious anemia, juvenile, due to selective intestinal malabsorption of vitamin b12, with proteinuria', 'MGA-1']",,261100,,,,C131677,,,,,,
mondo:0100157,Imerslund-Grasbeck syndrome type 2,"['megaloblastic anemia, Norwegian type', 'Imerslund-Grasbeck syndrome 2']",,618882,,,,,,,,,,
mondo:0100158,CHRNG-associated hypo-akinesia disorder of prenatal onset,,,,,,,,,,,,,
mondo:0100159,"pulmonary hypertension, neonatal",,,,,,,C4732,,,,,,
mondo:0100160,alcoholic ketoacidosis,"['alcoholic acidosis', 'alcoholic ketosis']",0080949,,,,,,,,,,,
mondo:0100161,hyperkalemic renal tubular acidosis,"['type 4 renal tubular acidosis', 'type 4 RTA', 'hyperkalemic RTA', 'renal tubular acidosis type 4']",,,89939,,,,,,,,,
mondo:0100162,IKBKG-related immunodeficiency with or without ectodermal dysplasia,['NEMO related ID/EDA-ID'],,,,,,,,,,,,
mondo:0100163,COVID-19–associated multisystem inflammatory syndrome in children,"['paediatric inflammatory multisystem syndrome', 'paediatric multisystem inflammatory syndrome', 'PIMS-TS', 'COVID-19 -related pediatric inflammatory multisystem syndrome', 'COVID-19 Kawasaki-like syndrome', 'COVID-19 associated multisystem inflammatory syndrome in children', 'SARS-CoV-2 Kawasaki-like syndrome', 'pediatric inflammatory multisystem syndrome', 'pediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2', 'multisystem inflammatory syndrome in children associated with coronavirus disease 2019', 'multisystem inflammatory syndrome in children', 'pediatric multi-system inflammatory syndrome potentially associated with COVID-19', 'pediatric inflammatory multisystem syndrome: temporally associated with SARS-CoV-2', 'PIMS', 'pediatric multisystem inflammatory syndrome', 'paediatric inflammatory multisystem syndrome: temporally associated with SARS-CoV-2', 'paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2', 'multisystem inflammatory syndrome in children associated with COVID-19', 'MIS-C', 'COVID-19 -related paediatric inflammatory multisystem syndrome', 'PMIS', 'paediatric multi-system inflammatory syndrome potentially associated with COVID-19']",0080711,,,,,C172127,,,,,,
mondo:0100164,permanent neonatal diabetes mellitus,"['monogenic diabetes of infancy', 'PNDM', 'PDMI', 'diabetes mellitus, permanent, of infancy', 'developmental delay, epilepsy, and neonatal diabetes', 'diabetes mellitus, permanent neonatal, with neurologic features', 'permanent diabetes mellitus of infancy', 'diabetes mellitus, permanent neonatal']",0060639,,99885,C1833104,"['0.7607', '-0.2273', '0.04147', '0.8164', '-0.4397', '-0.993', '-0.1816', '1.01', '0.2438', '-0.6094', '-0.1691', '-0.4463', '0.404', '0.03882', '-0.8936', '-0.4897', '0.3984', '0.0333', '0.03824', '-0.666', '0.2064', '-0.0698', '0.09534', '0.07465', '-0.534', '-0.308', '0.1096', '0.1404', '0.6045', '-0.555', '0.8745', '-0.2004', '0.2145', '0.0639', '-0.1296', '0.561', '-0.5996', '0.527', '-0.1389', '-0.1527', '0.05527', '0.4192', '0.2125', '0.2837', '-0.2345', '-0.4', '0.4163', '-0.2812', '0.007233', '0.192', '0.308', '-0.3362', '0.685', '-0.716', '0.03278', '0.3691', '-0.1799', '-0.6294', '-1.012', '0.4377', '-0.3208', '0.4834', '-0.1466', '0.1688', '0.084', '0.8696', '-0.4626', '0.513', '-0.97', '0.1444', '0.5576', '0.214', '0.0925', '-0.0509', '0.7056', '0.502', '-0.5366', '0.878', '-0.417', '-0.11865', '0.3604', '0.1108', '-0.1776', '-0.6772', '0.2377', '0.3254', '0.1788', '0.623', '0.7856', '0.3145', '0.5986', '0.1945', '-0.07855', '-0.2554', '1.26', '0.1848', '-0.2343', '-0.2747', '-0.236', '0.1504']",C114902,,C563425,,,,
mondo:0100165,permanent neonatal diabetes mellitus 1,"['diabetes mellitus, permanent, of infancy', 'PDMI', 'diabetes mellitus, permanent neonatal 1', 'PNDM1']",,606176,,,,,,,,,,
mondo:0100166,PPP2R1A-related intellectual disability,,,,,,,,,,,,,
mondo:0100167,"pulmonary disease, chronic obstructive, susceptibility to",,,,,,,,,,,,,
mondo:0100168,desmoid tumor caused by somatic mutation,,0111349,,,,,,,,,,,
mondo:0100169,"polyneuropathy, inflammatory demyelinating, chronic",['CIDP'],,,,,,,,,,,,
mondo:0100170,"restless legs syndrome, susceptibility to",,,,,,,,,,,,,
mondo:0100171,"psoriasis, susceptibility to",,,,,,,,,,,,,
mondo:0100172,"intellectual disability, autosomal dominant","['mental retardation, autosomal dominant', 'autosomal dominant intellectual disability']",,,,,,,,,,,,
mondo:0100173,"leukemia, acute myeloid, susceptibility to",,,,,,,,,,,,,
mondo:0100174,"age related macular degeneration, susceptibility to",,,,,,,,,,,,,
mondo:0100175,TTN-related myopathy,"['congenital myopathy related to TTN', 'TTN myopathy']",,,,,,,,,,,,
mondo:0100176,AP-4 deficiency syndrome,,,,,,,,,,,,,
mondo:0100177,"allergic rhinitis, susceptibility to","['allergic rhinitis, susceptibility to']",,607154,,,,,,,,,,
mondo:0100178,"dermatitis, atopic, susceptibility to",,,,,,,,,,,,,
mondo:0100179,"Hirschsprung disease, susceptibility to",,,,,,,,,,,,,
mondo:0100180,"diabetes mellitus, ketosis-prone","['diabetes mellitus, ketosis-prone, susceptibility to', 'diabetes mellitus, ketosis-prone', 'KPD']",,612227,,,,,,,,,,
mondo:0100181,"dermatitis, atopic, 1","['dermatitis, atopic, susceptibility to, 1', 'ATOD1']",,,,,,,,,,,,
mondo:0100182,"schizophrenia, susceptibility to",,,,,,,,,,,,,
mondo:0100183,"radioulnar synostosis, nonsyndromic, susceptibility to",,,179300,,,,,,,,,,
mondo:0100184,GTP cyclohydrolase I deficiency,['GTP-cyclohydrolase I deficiency'],,,,,,,,,,,,
mondo:0100185,immune reconstitution inflammatory syndrome,"['immune restoration disease', 'IRS', 'IRIS', 'IRD', 'immune reconstitution syndrome', 'immune reconstitution inflammatory syndrome associated with Kaposi sarcoma']",,,,,,C125712,,D054019,,,,
mondo:0100186,GTP cyclohydrolase I deficiency with hyperphenylalaninemia,"['hyperphenylalaninemia due to GTP cyclohydrolase deficiency', 'hyperphenylalaninemia, Bh4-deficient, type B', 'hyperphenylalaninemia, BH4-deficient, B', 'hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to GTP cyclohydrolase 1 deficiency', 'GTPCH deficiency', 'GTP cyclohydrolase 1 deficiency', 'GTP cyclohydrolase I deficiency', 'HPABH4B']",0112225,233910,2102,C0268467,"['-0.4116', '0.4316', '0.2776', '-0.096', '0.1247', '-0.2583', '-0.04068', '0.1808', '-0.2114', '0.06757', '0.02567', '0.3552', '0.0817', '0.0825', '0.01637', '0.1317', '0.105', '-0.4934', '-0.6323', '-0.7256', '-0.296', '-0.0711', '-0.0646', '0.1688', '-0.1417', '0.1755', '0.309', '0.0686', '-0.3706', '0.212', '-0.0706', '0.475', '0.2866', '0.1865', '-0.3787', '-0.06696', '-0.002996', '-0.3052', '0.0843', '-0.1135', '0.2712', '-0.05084', '-0.05106', '-0.12427', '-0.2852', '-0.4812', '0.307', '-0.1545', '0.1489', '0.6465', '-0.197', '-0.3318', '-0.3503', '-0.4563', '0.11597', '-0.0958', '0.3542', '0.2534', '-0.2974', '0.4048', '0.05472', '0.3777', '0.5737', '0.009674', '-0.03754', '0.08344', '0.5317', '-0.09717', '-0.1267', '0.09717', '-0.3306', '0.1216', '-0.2761', '-0.76', '0.3445', '0.456', '0.05286', '-0.2659', '-0.1633', '0.0365', '0.2391', '0.1685', '-0.03638', '-0.1763', '0.3599', '-0.3105', '0.1375', '-0.2372', '0.6826', '-0.0728', '-0.2063', '0.2773', '-0.1448', '-0.4155', '0.3374', '0.938', '0.1492', '-0.4229', '0.4685', '0.255']",C141442,,,,,,
mondo:0100187,opioid-induced constipation,['OIC'],,,,,,,,,,,,
mondo:0100188,combined ApoA-I and ApoC-III deficiency,"['ApoA-I and apoC-III deficiency, combined']",,,,,,,,,,,,
mondo:0100189,apolipoprotein A-I deficiency,"['ApoA-I deficiency', 'familial hypoalphalipoproteinemia', 'familial apoA-I deficiency']",,,425,,"['0.09106', '-0.4421', '-0.511', '0.328', '0.5796', '-0.0902', '-0.318', '0.787', '-0.29', '-0.1515', '-0.57', '-0.63', '-0.3604', '0.4595', '-0.1781', '-0.661', '0.3179', '-0.1968', '0.156', '-0.3752', '0.1343', '-0.0776', '0.1553', '-0.1512', '-0.2319', '0.3418', '0.2074', '0.8604', '0.03992', '-0.04718', '1.278', '0.12244', '0.6206', '0.274', '-0.1157', '-0.699', '-0.0889', '-0.3308', '-0.12036', '-0.731', '0.341', '0.2659', '1.099', '-0.2913', '-0.0491', '-0.2976', '0.05145', '0.1733', '-0.6523', '-0.09735', '0.5293', '-0.075', '0.04675', '-0.5146', '-0.299', '0.1556', '0.67', '-0.5474', '-0.3394', '-0.005398', '-0.311', '0.3516', '0.1449', '-0.475', '-0.05563', '-0.02876', '0.4304', '0.8374', '0.03342', '-0.2067', '-0.0326', '-0.2454', '-0.2917', '0.0558', '0.394', '0.1428', '0.1533', '-0.1653', '-0.03226', '-0.2888', '-0.3086', '-0.03305', '-0.4705', '0.451', '0.7056', '0.414', '0.03677', '-0.2793', '0.4446', '0.00514', '0.452', '-0.0824', '-0.189', '-0.2461', '0.793', '0.3665', '-0.07837', '0.2316', '-0.4949', '0.1069']",,,,,,,
mondo:0100190,gastric intestinal metaplasia,"['intestinal metaplasia', 'GIM']",,,,,,C8360,,,,,,
mondo:0100191,inherited kidney disorder,"['nephrogenetic disorder', 'inherited renal disorder', 'genetic renal disease', 'inherited kidney disease']",,,,,,,,,,,,
mondo:0100192,liver failure,['hepatic failure'],,,,,,C26922,,D017093,,,,
mondo:0100193,chronic liver failure,"['ESLD', 'end stage liver disease (decompensated liver disease)', 'end stage liver disease', 'end-stage liver disease']",,,,,,C84428,,,,,,
mondo:0100194,pregnancy associated osteoporosis,['pregnancy and lactation-associated osteoporosis'],,,,,,,,,,,,
mondo:0100195,X-linked intellectual disability with hypopituitarism,,,,,,,,,,,,,
mondo:0100196,TPM2-related myopathy,"['congenital myopathy related to TPM2', 'autosomal dominant TPM2-related myopathy', 'TPM2 myopathy']",,,,,,,,,,,,
mondo:0100197,parainfluenza infectious disease,"['parainfluenza (disorder)', 'parainfluenza infectious disorder', 'human parainfluenza virus infectious disorder', 'human parainfluenza viruses infectious disorder', 'HPIV infectious disorder']",,,,,,,,,,,,
mondo:0100198,Mendelian encephalopathy,,,,,,,,,,,,,
mondo:0100199,diffuse gastric and lobular breast cancer syndrome with or without cleft lip and/or palate,,,,,,,,,,,,,
mondo:0100200,microcephaly with intellectual disability,['microcephaly with neurodevelopmental phenotypes'],,,,,,,,,,,,
mondo:0100201,lumbar disk disease,,,,,,,,,,,,,
mondo:0100202,"lumbar disk herniation, susceptibility to",,,,,,,,,,,,,
mondo:0100203,parainfluenza virus type 1 infectious disease,"['infection caused by human parainfluenza virus 1', 'infection due to human parainfluenza virus 1', 'parainfluenza 1 infection']",,,,,,,,,,,,
mondo:0100204,parainfluenza virus type 2 infectious disease,"['infection due to human parainfluenza virus 2', 'infection caused by human parainfluenza virus 2']",,,,,,,,,,,,
mondo:0100205,parainfluenza virus type 4 infectious disease,"['infection caused by parainfluenza virus 4', 'infection due to parainfluenza virus 4', 'infection caused by human parainfluenza virus 4', 'infection due to human parainfluenza virus 4']",,,,,,,,,,,,
mondo:0100206,"lumbar disk degeneration, susceptibility to",,,,,,,,,,,,,
mondo:0100207,infantile-onset epilepsy,,,,,,,,,,,,,
mondo:0100208,self-limited familial neonatal-infantile epilepsy,,,,,,,,,,,,,
mondo:0100209,"X inactivation, familial skewed",,,,,,,,,,,,,
mondo:0100210,growth hormone insensitivity syndrome with immune dysregulation,,,,,,,,,,,,,
mondo:0100211,"growth hormone insensitivity with immune dysregulation 1, autosomal recessive","['Laron syndrome due to postreceptor defect', 'Laron syndrome with immunodeficiency', 'short stature due to STAT5b deficiency', 'Laron-like syndrome', 'growth hormone insensitivity due to postreceptor defect', 'growth hormone insensitivity with immunodeficiency']",0080836,245590,220465,C4510411,"['-0.1399', '0.1442', '0.1897', '-0.4993', '0.163', '0.002731', '0.2355', '0.862', '-0.394', '-0.2385', '0.12396', '0.2267', '-0.07556', '-0.2532', '0.2302', '0.005302', '0.5913', '0.1967', '-0.5117', '-0.2644', '0.576', '-0.4485', '0.535', '-0.446', '0.2161', '0.173', '0.03613', '0.03094', '0.4097', '-0.4', '0.1776', '0.00968', '0.587', '0.2158', '-0.14', '-0.2062', '-0.8823', '-0.01109', '-0.00835', '-0.0433', '-0.0002966', '-0.04694', '-0.2383', '-0.05737', '-0.09015', '-0.4104', '-0.0612', '0.04285', '-0.3635', '-0.191', '-0.02751', '-0.09656', '-0.1012', '0.2512', '-0.489', '-0.411', '-0.085', '-0.524', '0.001794', '0.2576', '0.0719', '0.566', '-0.4622', '-0.2532', '0.9897', '-0.266', '0.2932', '0.3162', '-0.6523', '0.5195', '-0.1924', '0.3127', '0.2014', '0.203', '-0.3457', '0.0937', '0.242', '-0.0672', '0.4016', '0.10175', '0.3516', '0.5063', '0.18', '0.2668', '-0.3372', '0.2411', '0.5786', '0.469', '0.2351', '0.2842', '0.4365', '0.66', '-0.08606', '-0.2988', '0.933', '1.053', '0.05728', '-0.3735', '-0.1353', '-0.075']",,,C537871,,,,
mondo:0100212,IFAP syndrome,,,,,,,,,,,,,
mondo:0100213,IFAP syndrome with or without BRESHECK syndrome,"['ichthyosis follicularis-alopecia-photophobia syndrome', 'IFAP/BRESHECK syndrome', 'IFAP syndrome with or without BRESHECK syndrome', 'ichthyosis follicularis, atrichia, and photophobia with or without brain anomalies, retardation, ectodermal dysplasia, skeletal malformations, Hirschsprung disease, Ear/eye anomalies, cleft palate/cryptorchidism, and kidney dysplasia/hypoplasia', 'ichthyosis follicularis-atrichia-photophobia syndrome', 'IFAP syndrome with or without BRESHECK syndrome, X-linked recessive', 'IFAP syndrome', 'ichthyosis follicularis atrichia photophobia syndrome']",0111821,308205,2273,C1839988,"['-0.4978', '0.4407', '-0.2651', '-0.6235', '0.309', '-0.5654', '-0.2754', '0.04547', '0.1063', '-0.3972', '0.343', '-0.1986', '-0.0635', '0.4907', '-0.439', '-0.01162', '0.22', '-0.07654', '-0.2344', '-1.0625', '-0.1779', '-0.03088', '0.2815', '-0.4397', '0.09125', '-0.02013', '-0.6973', '0.622', '0.182', '-0.2167', '0.4795', '-0.342', '0.1582', '0.2974', '0.3523', '-0.339', '-0.1926', '-0.52', '-0.09314', '0.5933', '0.2766', '-0.1213', '0.3047', '0.2627', '0.0645', '0.02638', '0.298', '-0.04898', '-0.1997', '-0.2085', '-0.302', '0.04446', '0.3413', '-0.2585', '-0.7583', '0.1428', '0.576', '-0.2047', '-0.2583', '-0.1109', '0.2252', '-0.1381', '-0.353', '0.3499', '0.2705', '0.3806', '0.7812', '0.7104', '0.1761', '0.5547', '0.255', '-0.522', '-0.0775', '-0.1082', '-0.1835', '0.11346', '0.5234', '-0.5757', '0.1522', '0.11487', '0.06525', '-0.1781', '-0.02126', '0.4546', '0.09674', '0.08923', '-0.232', '0.02095', '-0.4097', '0.396', '0.2651', '0.9507', '0.4626', '0.552', '0.533', '-0.2273', '0.2979', '-0.3118', '0.2488', '0.527']",,,C536085,,,,
mondo:0100214,Rajab interstitial lung disease with brain calcifications,,,,,,,,,,,,,
mondo:0100215,Rajab interstitial lung disease with brain calcifications 1,"['developmental delay, small stature, microcephaly, and brain calcifications', 'brain calcification, Rajab type', 'NEDBLLA', 'neurodevelopmental disorder with brain, liver, and lung abnormalities', 'Rajab syndrome']",,618007,178506,CN248515,"['-0.2795', '0.2852', '-0.08374', '-0.1127', '0.2588', '-0.2852', '-0.3923', '0.3882', '-0.2976', '0.3494', '-0.536', '-0.4487', '-0.16', '-0.268', '0.4204', '-0.3616', '0.412', '0.1437', '-0.3733', '-0.788', '0.1835', '-0.2817', '0.438', '-0.2659', '0.2683', '-0.1152', '-0.34', '-0.0389', '-0.3618', '0.0828', '0.654', '-0.1979', '-0.0295', '0.10046', '0.1937', '0.356', '-0.3938', '-0.1381', '0.03558', '-0.1857', '0.2495', '-0.529', '-0.2668', '-0.00452', '0.0729', '-0.579', '0.2164', '-0.1515', '-0.04645', '-0.652', '0.2578', '0.0869', '-0.2449', '-0.00221', '0.1475', '-0.633', '0.2986', '0.3115', '-0.1882', '0.166', '-0.04755', '-0.0409', '0.3218', '-0.00936', '-0.04004', '0.04037', '0.01785', '0.4668', '-0.6772', '0.5024', '-0.2166', '0.10187', '0.05856', '-0.00981', '-0.11707', '-0.1161', '-0.0366', '0.3096', '-0.0845', '-0.05148', '-0.1265', '0.05838', '-0.1504', '0.4788', '-0.0524', '-0.1572', '0.3953', '0.578', '0.1462', '0.1364', '0.1304', '0.5835', '0.03552', '0.1282', '0.412', '0.348', '0.4119', '-0.2761', '0.3481', '0.0606']",,,,,,,
mondo:0100216,DICER1-related tumor predisposition,,,,,,,,,,,,,
mondo:0100217,"developmental delay with short stature, dysmorphic facial features, and sparse hair 2","['DEDSSH2', 'diphthamide deficiency syndrome 2']",,620062,,,,,,,,,,
mondo:0100218,arthrogryposis multiplex congenita 5,"['AMC5', 'ARTHROGRYPOSIS MULTIPLEX CONGENITA 5']",0080981,618947,,,,,,,,,,
mondo:0100219,"growth hormone insensitivity syndrome with immune dysregulation 2, autosomal dominant","['GROWTH HORMONE INSENSITIVITY SYNDROME WITH IMMUNE DYSREGULATION 2, AUTOSOMAL DOMINANT', 'GHISID2', 'growth hormone insensitivity with immune dysregulation 2, autosomal dominant']",0080837,618985,,,,,,,,,,
mondo:0100220,Rajab interstitial lung disease with brain calcifications 2,"['RILDBC2', 'RAJAB INTERSTITIAL LUNG DISEASE WITH BRAIN CALCIFICATIONS 2']",,619013,,,,,,,,,,
mondo:0100221,IFAP syndrome 2,"['ichthyosis follicularis, atrichia, and photophobia syndrome 2', 'ichthyosis , follicular, with atrichia and photophobia syndrome 2', 'IFAP2', 'IFAP SYNDROME 2']",,619016,,,,,,,,,,
mondo:0100222,A20 haploinsufficiency,['HA20'],,,,,,,,,,,,
mondo:0100223,"mitochondrial complex I deficiency, nuclear type",,0112065,,,,,,,,,,,
mondo:0100224,"mitochondrial complex I deficiency, nuclear type 1","['mitochondrial NADH dehydrogenase component of Complex I, deficiency of', 'NADH:Q(1) oxidoreductase deficiency', 'MC1DN1', 'NADH-coenzyme Q reductase deficiency', 'mitochondrial complex I deficiency', 'mitochondrial complex 1 deficiency']",0112074,252010,,C1838979,,,,,,,,
mondo:0100225,collagen 6-related myopathy,"['collagen VI-related muscle disorder', 'collagen VI-related myopathy', 'collagen VI-related muscular dystrophy']",,,,,,,,,,,,
mondo:0100226,"parasomnia, sleepwalking type","['parasomnia, sleepwalking type, multifactorial', 'parasomnia, sleepwalking type', 'sleep walking', 'sleepwalking disorder', 'sleep walking disorder', 'somnambulism', 'PSMNSW', 'parasomnia, sleep terrors type']",,613938,,,,,,D013009,,,,
mondo:0100227,ALS2-related motor neuron disease,['Alsin-related motor neuron disease'],,,,,,,,,,,,
mondo:0100228,LAMA2-related muscular dystrophy,,,,,,,,,,,,,
mondo:0100230,fatty acyl-CoA reductase 1 dysregulation,"['FAR1 dysregulation', 'fatty acyl-CoA reductase 1 dysregulation']",,,,,,,,,,,,
mondo:0100231,"psoriatic arthritis, susceptibility to, 1","['psoriatic arthritis, susceptibility to, 1', 'psoriatic arthritis, susceptibility to', 'psoriatic arthritis susceptibility caused by LTA', 'PSORAS1']",,,,,,,,,,,,
mondo:0100232,"psoriatic arthritis, susceptibility to","['psoriatic arthritis, susceptibility', 'psoriatic arthritis, susceptibility to']",,607507,,,,,,,,,,
mondo:0100233,long COVID-19,"['PASC', 'long-haul COVID-19', 'post-acute sequelae of COVID-19', 'post-acute sequelae of SARS-CoV-2 infection', 'sequelae of COVID-19', 'long haul COVID-19']",0080848,,,C5433293,,C179263,,D000094024,,,10085504,
mondo:0100234,paroxysmal familial ventricular fibrillation,"['paroxysmal familial ventricular fibrillation', 'IVF', 'idiopathic ventricular fibrillation, non Brugada type', 'paroxysmal ventricular fibrillation', 'ventricular fibrillation, paroxysmal familial', 'idiopathic ventricular fibrillation']",,,228140,,"['0.011505', '0.00992', '-0.0463', '-0.0122', '0.0933', '-0.1869', '0.5103', '0.3203', '0.0855', '-0.0706', '-0.09735', '-0.2153', '-0.1149', '-0.095', '-0.1405', '-0.2013', '-0.3113', '-0.1471', '-0.1661', '-0.3289', '0.2274', '0.187', '0.2128', '0.01002', '0.1478', '-0.0686', '0.3665', '-0.1162', '0.218', '0.1488', '0.3625', '0.0689', '0.4119', '0.1431', '0.00965', '-0.3943', '0.2394', '-0.1605', '0.08984', '-0.5127', '0.0456', '-0.06088', '0.2617', '-0.0974', '-0.07043', '-0.132', '-0.197', '0.4365', '-0.1985', '0.154', '-0.075', '-0.00748', '-0.05234', '-0.0856', '-0.3218', '0.0309', '0.00782', '-0.06525', '-0.2903', '-0.1539', '0.086', '0.1917', '0.209', '-0.1891', '0.1278', '0.1577', '0.3179', '0.1824', '-0.437', '0.2377', '-0.214', '0.10785', '-0.00105', '-0.1417', '-0.03604', '-0.05432', '0.01674', '-0.0752', '-0.294', '-0.2053', '-0.0948', '0.1277', '0.01648', '0.05493', '-0.05325', '-0.3835', '0.2347', '0.12354', '-0.02652', '0.05194', '0.0715', '-0.0694', '-0.03024', '0.0728', '0.2917', '0.0978', '0.546', '-0.501', '-0.5312', '-0.01839']",,,,,,,
mondo:0100235,FOXC1-related anterior segment dysgenesis,,,,,,,,,,,,,
mondo:0100236,LTBP2-related ocular dysgenesis,,,,,,,,,,,,,
mondo:0100237,inherited cutis laxa,['hereditary cutis laxa'],,,,,,,,,,,,
mondo:0100238,inherited Fanconi renotubular syndrome,['hereditary Fanconi renotubular syndrome'],,,,,,,,,,,,
mondo:0100239,inherited hypertrophic pyloric stenosis,['hereditary hypertrophic pyloric stenosis'],,,,,,,,,,,,
mondo:0100240,inherited thrombophilia,"['thrombophilia, hereditary', 'hereditary hypercoagulable disorder', 'hereditary thrombophilia']",,,,,,,,,,,,
mondo:0100241,inherited thrombocytopenia,['hereditary thrombocytopenia'],,,,,,,,,,,,
mondo:0100242,glioma susceptibility,"['glioma, susceptibility to', 'glioma, susceptibility']",,,,,,,,,,,,
mondo:0100244,paroxysmal nocturnal hemoglobinuria,"['hereditary paroxysmal nocturnal hemoglobinuria', 'Marchiafava-Micheli disease', 'paroxysmal hemoglobinuria', 'PNH', 'acquired paroxysmal nocturnal hemoglobinuria', 'inherited paroxysmal nocturnal hemoglobinuria']",0060284,,447,C0024790,"['-0.01822', '0.1757', '-0.0455', '-0.06396', '-0.0909', '-0.2164', '0.1847', '0.003187', '-0.06158', '-0.03223', '0.02911', '-0.03217', '0.03195', '-0.0609', '-0.1019', '-0.01633', '-0.07336', '-0.1615', '-0.0116', '-0.324', '0.0637', '-0.02592', '0.05173', '-0.1027', '0.05548', '-0.06445', '0.0476', '-0.1227', '0.003511', '-0.07355', '0.0672', '0.1257', '0.2244', '0.10156', '-0.0209', '-0.03023', '0.0808', '-0.09357', '-0.04062', '-0.251', '0.1292', '-0.1907', '0.05093', '0.04718', '0.0681', '-0.1407', '-0.1381', '0.1625', '0.1545', '0.2128', '-0.0545', '0.001064', '-0.05594', '-0.003004', '0.07275', '-0.1289', '0.3115', '-0.05637', '-0.1694', '0.0645', '0.08704', '0.05334', '0.1473', '0.02753', '-0.1254', '0.02362', '0.2233', '0.02179', '-0.1848', '0.1744', '-0.2556', '0.0949', '0.03069', '-0.1279', '0.03494', '0.1226', '0.0856', '-0.010056', '-0.2479', '-0.0915', '0.003574', '0.1396', '0.01245', '0.1126', '0.03415', '-0.03558', '0.09094', '0.1406', '0.1342', '0.04007', '-0.010056', '0.06506', '0.0466', '0.08875', '0.1884', '0.10803', '0.2413', '-0.2551', '-0.0913', '0.0359']",C61233,,,,,10034042,0004818
mondo:0100246,"migraine with or without aura, susceptibility to","['migraine with or without aura, susceptibility', 'migraine with or without aura, susceptibility to']",,,,,,,,,,,,
mondo:0100247,multiple congenital anomalies-hypotonia-seizures syndrome,,0080503,,,,,,,,,,,
mondo:0100248,rapidly progressive primary central nervous system vasculitis,['rapidly progressive PCNSV'],,,,,,,,,,,,
mondo:0100249,"46,XX testicular disorder of sex development","['XX male syndrome', 'De la Chapelle syndrome', '46,XX testicular DSD', 'XX sex reversal', '46, XX gonadal sex reversal', '46,XX testicular disorders of Sex development', 'XX Male, Sry-positive', '46,XX testicular disorder of sex development', '46,XX testicular differences of sex development', 'XX, male syndrome']",0111760,,393,CN205000,"['-0.5117', '-0.2131', '-0.4019', '-0.4136', '0.514', '-0.008255', '0.0868', '0.6104', '-0.655', '-0.0944', '0.2964', '0.07477', '0.1909', '0.6294', '-0.02223', '-0.0362', '0.4167', '0.387', '-0.828', '-0.775', '-0.4832', '-0.1099', '0.8896', '-0.5938', '0.7026', '-0.161', '-0.1769', '-0.0184', '0.4915', '-0.4573', '1.053', '-0.2438', '0.567', '-0.03915', '-0.3254', '-0.73', '-0.00874', '-0.4077', '-0.178', '-0.0413', '0.4949', '0.2615', '0.11865', '-0.1763', '0.597', '-0.8413', '-0.2014', '-0.4702', '0.01776', '0.4343', '-0.003748', '-0.2947', '-0.8115', '-0.03247', '-0.09406', '0.535', '0.1729', '-0.7866', '-0.2234', '0.1323', '0.1573', '0.561', '-0.0357', '0.2754', '0.02771', '0.8315', '0.1857', '0.5186', '-0.367', '0.4028', '-0.791', '0.1941', '0.2524', '-0.10565', '0.3215', '-0.741', '0.1874', '-0.1913', '-0.6475', '-0.3936', '0.4165', '0.2827', '0.348', '-0.11676', '-0.3506', '0.12427', '0.1456', '-0.3152', '0.5186', '-0.4434', '-0.4387', '0.3347', '-0.629', '-0.2368', '0.521', '-0.2418', '0.3704', '0.0395', '0.1764', '-0.0959']",C127170,,D058531,,,,
mondo:0100250,"46,XX sex reversal 1","['46XX sex reversal 1, X-linked dominant', '46,XX Sex reversal, SRY-positive', '46,XX gonadal dysgenesis, complete, SRY-positive', '46,XX Sex reversal type 1', 'ovotesticular DSD', 'SRXX1', '46,XX true hermaphroditism, SRY-positive', 'ovotesticular disorder of sex development', '46,XX SEX reversal 1']",0111761,400045,,,,C179867,,,,,,
mondo:0100251,familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome,"['hyperphosphatemia tumoral calcinosis', 'hyperphosphatemic familial tumoral calcinosis', 'morbus Teutschlaender', 'hyperostosis with hyperphosphatemia', 'primary hyperphosphatemic tumoral calcinosis', 'tumoral calcinosis, hyperphosphatemic, familial, 1', 'hyperphosphatemia hyperostosis syndrome', 'hypercalcemic tumoral calcinosis', 'hyperphosphatemia hyperostosis', 'cortical hyperostosis with hyperphosphatemia', 'tumoral calcinosis with hyperphosphatemia', 'HHS', 'lipocalcinogranulomatosis', 'familial hyperphosphatemic tumoral calcinosis/hyperphosphatemic hyperostosis syndrome', 'HFTC', 'familial Teutschlaender disease', 'PHPTC']",0111063,,306661,C1876187,"['-0.34', '0.269', '0.0549', '-0.2292', '0.369', '-0.1823', '-0.366', '0.0964', '-0.5405', '0.09796', '-0.3054', '0.3083', '-0.0653', '-0.1868', '-0.12036', '-0.1306', '0.1392', '-0.2092', '0.2079', '-0.2656', '0.1135', '-0.3784', '0.628', '-0.1201', '0.2003', '0.3472', '0.1348', '-0.01077', '0.06555', '-0.285', '-0.01735', '-0.1865', '0.089', '-0.003248', '0.01532', '-0.2795', '-0.10364', '0.08075', '0.1906', '-0.5303', '0.2217', '-0.4668', '0.2006', '-0.003462', '0.0437', '-0.4038', '0.276', '0.2173', '0.4607', '0.0224', '0.01938', '-0.08356', '0.2019', '0.1477', '-0.309', '-0.6235', '0.4126', '0.095', '-0.675', '0.3196', '0.39', '0.1262', '-0.442', '-0.3691', '0.3618', '-0.01147', '0.357', '0.4011', '-0.0773', '-0.2108', '-0.2598', '-0.2153', '0.06555', '-0.08496', '-0.01596', '0.2568', '-0.08685', '0.5356', '-0.04556', '-0.24', '-0.1781', '0.1328', '0.10394', '-0.1517', '-0.0547', '-0.07306', '0.02391', '0.322', '0.0885', '-0.02953', '-0.1144', '0.1292', '0.06714', '-0.4995', '0.3555', '0.1131', '0.5103', '-0.4607', '-0.1438', '0.0966']",C131851,,,,,,
mondo:0100252,"tumoral calcinosis, hyperphosphatemic, familial, 1","['hyperostosis-hyperphosphatemia syndrome', 'tumoral calcinosis, primary Hyperphosphatemic', 'tumoral calcinosis, hyperphosphatemic, familial', 'calcinosis, tumoral, with hyperphosphatemia', 'Morbus Teutschlaender', 'tumoral calcinosis, HYPERPHOSPHATEMIC, familial, 1', 'HFTC1', 'HFTC', 'tumoral calcinosis, Hyperphosphatemic, familial, 1', 'Teutschlaender disease, familial']",,211900,,,,,,,,,,
mondo:0100253,Roberts-SC phocomelia syndrome,"['Roberts-SC phocomelia syndrome', 'phocomelia-pseudothalidomide syndrome', 'pseudothalidomide syndrome', 'RBS', 'long bone deficiencies associated with cleft lip-palate']",,268300,,,,C4681,,,,,,
mondo:0100254,CACNA1A-related complex neurodevelopmental disorder,,,,,,,,,,,,,
mondo:0100255,adenosine kinase deficiency,"['ADK hypermethioninemia', 'MRT8', 'ADK deficiency', 'hypermethioninemia encephalopathy due to ADK deficiency', 'autosomal recessive mental retardation 8', 'autosomal recessive intellectual disability 8', 'mental retardation, autosomal recessive 8, formerly', 'mental retardation, autosomal recessive 8; MRT8', 'mental retardation, autosomal recessive 8', 'adenosine kinase deficiency', 'hypermethioninemia due to adenosine kinase deficiency', 'hypermethioninemia encephalopathy due to adenosine kinase deficiency']",0111038,614300,289290,C3280381,"['-0.757', '0.10254', '-0.1262', '-0.2515', '0.222', '-0.1888', '0.377', '0.478', '-0.638', '0.6235', '-0.298', '-0.413', '0.3037', '-0.1417', '-0.3188', '-0.3196', '-0.1519', '-0.1082', '-0.574', '-0.796', '0.5503', '0.1686', '0.906', '0.07294', '-0.01018', '-0.237', '0.4802', '0.05862', '0.4072', '0.3938', '0.443', '0.34', '0.511', '0.1688', '0.1301', '-0.3733', '-0.4326', '0.08673', '-0.12494', '-0.2954', '0.284', '-0.1195', '0.5864', '0.0237', '-0.636', '0.2803', '0.2037', '0.2234', '-0.4688', '0.4153', '-0.1987', '0.1135', '-0.02231', '0.4392', '-0.04266', '-0.1125', '-0.004154', '-0.485', '-0.06305', '0.4685', '-0.1133', '0.1873', '0.5254', '-0.4104', '0.1321', '0.2646', '0.488', '0.4783', '-0.8984', '0.1582', '-0.571', '0.703', '-0.256', '0.2236', '-0.3638', '0.03763', '0.801', '-0.7397', '-0.04916', '-0.08606', '0.10345', '-0.1212', '-0.1643', '0.0517', '0.2854', '0.7417', '-0.4058', '0.63', '0.4858', '0.3328', '0.2433', '0.1348', '0.3171', '-0.2656', '0.811', '0.471', '0.495', '-0.452', '0.3594', '0.2542']",,,C567015,,,,
mondo:0100256,CTNNA1-related diffuse gastric and lobular breast cancer syndrome,,,,,,,,,,,,,
mondo:0100257,peroxisomal single enzyme/protein defect,['peroxisomal single enzyme/protein defect'],,,,,,,,,,,,
mondo:0100258,phytanoyl-CoA hydroxylase deficiency,"['PHYH related disorder of peroxisomal alpha oxidation', 'phytanoyl-CoA hydroxylase deficiency', 'PHYH deficiency']",,,,,,,,,,,,
mondo:0100259,peroxisome biogenesis disorder due to PEX1 defect,"['PEX1 related Zellweger spectrum disorder', 'peroxisome biogenesis disorder due to PEX1 defect']",,,,,,,,,,,,
mondo:0100260,peroxisome biogenesis disorder due to PEX2 defect,"['peroxisome biogenesis disorder due to PEX2 defect', 'PEX2 related Zellweger spectrum disorder']",,,,,,,,,,,,
mondo:0100261,peroxisome biogenesis disorder due to PEX3 defect,"['PEX3 related Zellweger spectrum disorder', 'peroxisome biogenesis disorder due to PEX3 defect']",,,,,,,,,,,,
mondo:0100262,peroxisome biogenesis disorder due to PEX5 defect,"['PEX5 related Zellweger spectrum disorder', 'peroxisome biogenesis disorder due to PEX5 defect']",,,,,,,,,,,,
mondo:0100263,peroxisome biogenesis disorder due to PEX6 defect,"['peroxisome biogenesis disorder due to PEX6 defect', 'PEX6 related Zellweger spectrum disorder']",,,,,,,,,,,,
mondo:0100264,peroxisome biogenesis disorder due to PEX10 defect,"['peroxisome biogenesis disorder due to PEX10 defect', 'PEX10 related Zellweger spectrum disorder']",,,,,,,,,,,,
mondo:0100265,peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain,['peroxisome biogenesis disorder due to PEX5 defect in the PEX7-binding domain'],,,,,,,,,,,,
mondo:0100266,peroxisome biogenesis disorder due to PEX12 defect,"['PEX12 related Zellweger spectrum disorder', 'peroxisome biogenesis disorder due to PEX12 defect']",,,,,,,,,,,,
mondo:0100267,peroxisome biogenesis disorder due to PEX13 defect,"['PEX13 related Zellweger spectrum disorder', 'peroxisome biogenesis disorder due to PEX13 defect']",,,,,,,,,,,,
mondo:0100268,peroxisome biogenesis disorder due to PEX14 defect,"['peroxisome biogenesis disorder due to PEX14 defect', 'PEX14 related Zellweger spectrum disorder']",,,,,,,,,,,,
mondo:0100269,peroxisome biogenesis disorder due to PEX16 defect,"['peroxisome biogenesis disorder due to PEX16 defect', 'PEX16 related Zellweger spectrum disorder']",,,,,,,,,,,,
mondo:0100270,peroxisome biogenesis disorder due to PEX19 defect,"['peroxisome biogenesis disorder due to PEX19 defect', 'PEX19 related Zellweger spectrum disorder']",,,,,,,,,,,,
mondo:0100271,peroxisome biogenesis disorder due to PEX26 defect,"['PEX26 related Zellweger spectrum disorder', 'peroxisome biogenesis disorder due to PEX26 defect']",,,,,,,,,,,,
mondo:0100272,peroxisome biogenesis disorder due to PEX7 defect,"['rhizomelic chondrodysplasia punctata type 1 (formerly)', 'adult refsum disease due to PEX7 defect (formerly)', 'PEX7 related peroxisome biogenesis disorder']",,,,,,,,,,,,
mondo:0100273,glyceronephosphate O-acyltransferase deficiency,"['GNPAT deficiency', 'glyceronephosphate O-acyltransferase deficiency']",,,,,,,,,,,,
mondo:0100274,alkylglycerone-phosphate synthase deficiency,"['alkylglycerone-phosphate synthase deficiency', 'AGPS deficiency']",,,,,,,,,,,,
mondo:0100275,fatty acyl-CoA reductase defects,"['FAR1 defect', 'fatty acyl-CoA reductase defects']",,,,,,,,,,,,
mondo:0100276,disorder of defective peroxisomal and mitochondrial fission,"['disorder of defective peroxisomal and mitochondrial fission', 'peroxisome and mitochronrial fission disease']",,,,,,,,,,,,
mondo:0100277,disorder of peroxisomal alpha oxidation,['disorder of peroxisomal alpha oxidation'],,,,,,,,,,,,
mondo:0100278,alanine glyoxylate aminotransferase deficiency,"['AGXT deficiency', 'AGXT defect', 'alanine glyoxylate aminotransferase deficiency']",,,,,,,,,,,,
mondo:0100279,peroxisome biogenesis disorder due to PEX11B defect,"['peroxisome biogenesis disorder due to PEX11B defect', 'PEX11B related peroxisome biogenesis disorder']",,,,,,,,,,,,
mondo:0100280,Waldenstrom macroglobulinemia,"['Waldenstroem^s macroglobulinemia', 'macroglobulinemia of Waldenstrom', 'Waldenström macroglobulinemia', 'Waldenstrom^s syndrome', 'lymphoplasmacytic lymphoma with IgM gammopathy', 'Waldenstrom^s macroglobulinaemia', 'Waldenstrom macroglobulinemia', 'Waldenstrom^s macroglobulinemia']",0060901,,33226,C0024419,,C80307,,D008258,,C88.0,10047801,
mondo:0100281,"macroglobulinemia, Waldenstrom, 1","['macroglobulinemia, Waldenstrom, somatic', 'macroglobulinemia, waldenstrom, susceptibility to, 1', 'WM1']",,153600,,,,,,,,,,
mondo:0100282,SC phocomelia syndrome,['hypomelia hypotrichosis facial hemangioma syndrome'],0050536,269000,3103,,,,,,,,,
mondo:0100283,overgrowth syndrome and/or cerebral malformations due to abnormalities in MTOR pathway genes,,,,,,,,,,,,,
mondo:0100284,X-linked intellectual disability,,,,,,,,,,,,,
mondo:0100285,extrahepatic biliary atresia,"['EHBA', 'biliary atresia, extrahepatic']",,210500,,C4520983,,C97069,,,,,,
mondo:0100286,respiratory syncytial virus bronchiolitis,['RSV bronchiolitis'],,,,,,,,,,,,
mondo:0100287,POLE-related polyposis and colorectal cancer syndrome,,,,,,,,,,,,,
mondo:0100288,enhanced S-cone syndrome,"['retinoschisis with early nyctalopia', 'ESCS', 'enhanced S-cone syndrome']",0090059,268100,53540,C1849394,,,,C564835,,H35.5,,
mondo:0100289,Goldmann-Favre syndrome,"['retinoschisis with early nyctalopia', 'Favre hyaloideoretinal Degeneration']",,,53540,,"['-1.068', '-0.2517', '-0.128', '-0.06635', '0.0465', '-0.2253', '-0.4536', '0.761', '-0.0783', '-0.3645', '-0.08044', '-0.358', '-0.7935', '0.0407', '-0.287', '0.1346', '0.7764', '0.3386', '0.1131', '-0.4197', '-0.1438', '-0.04593', '-0.2277', '0.1327', '-0.1625', '0.4568', '-0.08215', '-0.1798', '-0.0834', '0.2032', '0.667', '-0.066', '0.3542', '0.2773', '0.1746', '0.405', '0.06946', '-0.4207', '0.06042', '-0.3591', '0.0712', '-0.3245', '0.01317', '-0.2585', '-0.307', '0.02722', '-0.07886', '-0.1606', '-0.07477', '0.1499', '0.807', '0.05984', '0.08484', '-0.2883', '0.1771', '-0.1055', '0.9956', '-0.2059', '-0.547', '-0.167', '0.3218', '-0.445', '0.09735', '0.49', '-0.0789', '-0.4119', '0.807', '1.133', '0.1296', '0.703', '-0.2605', '0.3586', '-0.1855', '-0.2087', '0.8613', '0.013885', '0.2065', '0.467', '-0.1705', '-0.1747', '0.566', '0.1364', '0.187', '1.061', '-0.1203', '-0.3887', '0.1749', '0.05206', '0.1409', '0.0014105', '0.49', '0.2201', '-0.06146', '0.4587', '0.3193', '0.1504', '0.7793', '-0.1844', '-0.03726', '0.0916']",,,,,H35.5,,
mondo:0100290,colon serrated polyposis,,,,,C3272797,,C96470,,,,,,
mondo:0100291,early T cell progenitor acute lymphoblastic leukemia,"['early T acute lymphoblastic leukaemia', 'ETP-ALL', 'early T-cell precursor acute lymphoblastic leukemia', 'early T-cell precursor lymphoblastic leukaemia', 'ETP ALL', 'early T-cell precursor lymphoblastic leukemia', 'early T acute lymphoblastic leukemia', 'early T-cell precursor acute lymphoblastic leukaemia']",,,,C4329780,,C130043,,,,,,
mondo:0100292,Carey-Fineman-Ziter syndrome 2,['CFZS2'],,619941,,,,,,,,,,
mondo:0100293,diaphragmatic malformation,,,,,,,,,,,,,
mondo:0100294,"mitochondrial complex II deficiency, nuclear type 1","['isolated succinate-ubiquinone reductase deficiency', 'complex 2 mitochondrial respiratory chain deficiency', 'isolated succinate-coenzyme Q reductase deficiency', 'succinate dehydrogenase deficiency', 'isolated succinate-CoQ reductase deficiency', 'isolated mitochondrial respiratory chain complex II deficiency', 'mitochondrial complex II deficiency', 'mitochondrial respiratory chain complex II deficiency', 'succinate CoQ reductase deficiency', 'mitochondrial complex 2 deficiency']",0060537,252011,3208,,"['-0.4268', '0.3337', '-0.2146', '0.1578', '-0.01344', '0.04135', '0.05344', '0.05115', '-0.2988', '-0.2927', '0.4314', '-0.292', '0.2896', '0.0763', '0.04364', '-0.1547', '-0.583', '-0.03333', '-0.4556', '-0.4033', '-0.0627', '-0.3137', '0.475', '0.1311', '0.03085', '-0.03778', '-0.0907', '0.02898', '-0.06805', '0.371', '0.3477', '0.2078', '0.6206', '-0.04727', '-0.2092', '-0.3745', '-0.04694', '0.07214', '0.338', '-0.1763', '-0.3176', '-0.3582', '0.0297', '0.3994', '-0.4167', '-0.3105', '0.1278', '-0.10175', '0.09265', '0.1277', '0.1126', '-0.2773', '0.00519', '0.0851', '-0.1465', '0.013855', '0.2715', '0.1564', '0.0189', '0.2532', '-0.1979', '-0.03677', '0.701', '0.2942', '-0.6445', '0.3', '0.0494', '0.4792', '-0.366', '0.251', '-0.1104', '0.1167', '-0.1299', '0.2595', '0.3318', '0.1964', '0.1114', '0.12335', '0.02214', '-0.2278', '0.03894', '0.2415', '0.073', '-0.07996', '0.1621', '0.1135', '-0.02591', '0.2556', '0.4211', '0.1371', '0.2261', '0.11194', '-0.3691', '-0.0948', '0.6855', '0.61', '0.1516', '-0.11383', '0.11035', '0.09174']",,,C565375,277.6,,,
mondo:0100295,"Alzheimer disease, susceptibility to, mitochondrial","['Alzheimer disease, susceptibility to, mitochondrial']",,502500,,,,,,,,,,
mondo:0100296,Olmsted syndrome 1,"['Olmsted syndrome', 'palmoplantar keratoderma, mutilating, with periorificial keratotic plaques 1']",0112013,614594,,,,,,,,,,
mondo:0100297,"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 1","['SSFSC', 'short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies']",,617877,,CN807949,,,,,,,,
mondo:0100298,abdominal wall malformation,,,,,,,,,,,,,
mondo:0100299,PAX5-related B lymphopenia and autism spectrum disorder,['hypogammaglobulinemia and autism spectrum disorder'],,,,,,,,,,,,
mondo:0100301,"hemangioma, capillary infantile, susceptibility to",,,602089,,,,,,,,,,
mondo:0100302,LADD syndrome 1,"['LADD1', 'lacrimoauriculodentodigital syndrome 1']",,149730,,,,,,,,,,
mondo:0100303,"ichthyosis, annular epidermolytic 1",,,607602,,,,,,,,,,
mondo:0100304,disorder of bile acid aminotransferase,['disorder of bile acid aminotransferase'],,,,,,,,,,,,
mondo:0100305,bile acid CoA:amino acid N-acyltransferase deficiency,"['BAAT deficiency', 'bile acid CoA:amino acid N-acyltransferase deficiency']",,,,,,,,,,,,
mondo:0100306,disorder of defective peroxisome oxidative status,['disorder of defective peroxisome oxidative status'],,,,,,,,,,,,
mondo:0100307,adult Refsum disease due to PEX7 defect,['adult Refsum disease due to PEX7 defect'],,,,,,,,,,,,
mondo:0100308,atactic disorder,"['ataxia', 'ataxic disorder']",,,,,,,,,,,,
mondo:0100309,hereditary ataxia,"['SCA', 'rare hereditary ataxia']",0050951,,183518,,"['-0.09814', '0.11664', '-0.1537', '0.0635', '0.0479', '-0.2585', '-0.08405', '0.05933', '-0.2352', '-0.0821', '0.0807', '0.0216', '0.07666', '-0.0768', '0.01269', '-0.1683', '-0.07404', '-0.077', '-0.1317', '-0.4006', '0.000907', '-0.1097', '0.0671', '-0.0814', '0.1456', '0.00302', '0.1043', '-0.04053', '0.10675', '-0.0705', '0.1567', '0.05737', '0.126', '0.008194', '-0.1302', '-0.0424', '-0.00891', '-0.1139', '-0.00962', '-0.2219', '0.101', '-0.2231', '0.1323', '-0.04697', '0.015175', '-0.33', '-0.0612', '0.02538', '0.2717', '-0.01033', '-0.03079', '-0.07184', '-0.1223', '0.10016', '0.01389', '-0.2153', '0.339', '0.1051', '-0.395', '-0.02815', '0.2479', '0.0688', '0.1891', '0.1305', '-0.0875', '0.08093', '0.2277', '0.1396', '-0.2048', '0.2498', '-0.2617', '-0.01714', '0.03076', '-0.01987', '0.1594', '0.2024', '0.04086', '0.134', '-0.2192', '-0.0662', '-0.01595', '0.1276', '-0.05133', '0.1247', '-0.03723', '-0.02731', '0.04602', '0.0968', '0.1037', '0.0319', '-0.02855', '0.1771', '-0.03455', '0.00854', '0.289', '0.1823', '0.2091', '-0.2896', '-0.05154', '0.0832']",,,C531684,,G11,,
mondo:0100310,hereditary cerebellar ataxia,"['hereditary cerebellar ataxia', 'cerebellar hereditary ataxia']",,,,,,C140268,,,,,,
mondo:0100311,sensory ataxia,,,,,,,,,,,,,
mondo:0100312,vestibular ataxia,,,,,,,,,,,,,
mondo:0100313,focal segmental glomerulosclerosis,"['focal glomerulosclerosis', 'FGS', 'FSGS', 'FSGS - focal segmental glomerulosclerosis', 'focal glomerular sclerosis', 'FGS (focal glomerular sclerosis)']",1312,,,CN043606,,C37308,,D005923,582.1,,,
mondo:0100314,GYG1-related disorder of glycogen metabolism,,,,,,,,,,,,,
mondo:0100315,isolated adrenal insufficiency,['isolated adrenal insufficiency'],,,,,,,,,,,,
mondo:0100316,long QT syndrome 1,"['ventricular fibrillation with prolonged QT interval', 'long QT syndrome 1/2, digenic', 'long QT syndrome type 1', 'long QT syndrome 1, acquired, susceptibility to', 'long QT syndrome 1', 'LQT1']",0110644,192500,,,,C85049,,,,,10039211,
mondo:0100317,deficiency of adenosine deaminase 2,,,,,,,,,,,,,
mondo:0100319,COVID-19–associated multisystem inflammatory syndrome in adults,['MIS-A'],,,,,,,,,,,,
mondo:0100320,post-COVID-19 disorder,,,,,,,,,,,,,
mondo:0100322,non-Zellweger spectrum disorder,['non-Zellweger spectrum disorder'],,,,,,,,,,,,
mondo:0100323,inherited pseudohypoaldosteronism,['hereditary pseudohypoaldosteronism'],,,,,,,,,,,,
mondo:0100324,primary focal segmental glomerulosclerosis,,,,,,,,,,,,,
mondo:0100325,odontochondrodysplasia 1,"['ODCD', 'spondylometaphyseal dysplasia with dentinogenesis imperfecta', 'odontochondrodysplasia', 'Goldblatt syndrome', 'chondrodysplasia-dentinogenesis imperfecta-joint laxity syndrome', 'Goldblatt chondrodysplasia']",,184260,166272,CN200045,"['-0.2505', '0.1794', '0.1985', '-0.569', '-0.09735', '-0.634', '-0.3035', '0.303', '-0.4275', '-0.1046', '-0.4387', '-0.1545', '-0.3228', '-0.02733', '0.153', '0.1665', '0.03903', '-0.003986', '-0.212', '-0.462', '-0.167', '0.4224', '0.6514', '-0.07733', '0.10223', '0.10876', '-0.2201', '-0.2327', '0.546', '0.0608', '-0.04865', '-0.3572', '-0.04456', '0.0761', '0.8486', '-0.1428', '0.01274', '-0.6875', '-0.1299', '-0.2927', '-0.3115', '-0.6987', '0.1292', '-0.0337', '0.0374', '-0.497', '-0.1942', '0.5967', '0.0732', '-0.297', '0.3655', '0.02557', '-0.1239', '0.1403', '-0.6147', '-0.54', '-0.1259', '-0.3965', '0.1436', '0.0388', '0.4785', '-0.129', '-0.4578', '0.0364', '-0.2512', '-0.5103', '0.03156', '0.5103', '-0.4277', '0.357', '-0.5146', '-0.04752', '0.274', '-0.1523', '-0.1368', '0.1469', '-0.2925', '-0.02736', '-0.2426', '-0.2754', '0.11896', '0.496', '-0.02753', '0.5674', '-0.1539', '0.2231', '0.0928', '0.325', '0.10126', '0.1858', '-0.2676', '0.0985', '-0.0451', '0.3948', '0.9995', '0.362', '0.5522', '-0.3262', '0.3484', '-0.1344']",,,,,,,
mondo:0100326,Glanzmann thrombasthenia,,,,849,,"['-0.0219', '0.03818', '0.004623', '-0.01929', '0.0003035', '-0.03787', '0.0016575', '0.03595', '-0.0381', '-0.02238', '-0.02092', '-0.01596', '0.0001596', '0.01508', '-0.02487', '-0.0187', '-0.00841', '-0.02061', '-0.00952', '-0.0891', '0.004246', '-0.02217', '0.0279', '0.00875', '0.01868', '-0.002977', '-0.004383', '0.001723', '-0.01124', '-0.01317', '0.017', '-0.01936', '0.0452', '0.01985', '0.01281', '-0.01453', '-0.01447', '-0.0218', '0.001769', '-0.04944', '0.01648', '-0.03278', '0.02893', '-0.00424', '0.001481', '-0.0444', '-0.00858', '0.03796', '0.0066', '0.02786', '-0.003876', '0.008255', '0.013855', '0.01727', '-0.03687', '-0.02039', '0.05176', '-0.01773', '-0.0702', '0.002638', '0.02615', '0.0354', '-0.01437', '0.001847', '0.002218', '0.000862', '0.04916', '0.02388', '-0.02777', '0.04916', '-0.03793', '-0.00257', '0.0007057', '-0.03607', '0.004463', '0.02759', '0.02419', '-0.005817', '-0.02519', '-0.01991', '-0.006924', '0.00983', '-0.005173', '0.0352', '0.00883', '0.007008', '0.00903', '0.03827', '0.0674', '0.004726', '0.02844', '0.03662', '0.01009', '0.01888', '0.0778', '0.02843', '0.0423', '-0.05432', '0.001037', '0.02734']",,,,,,,
mondo:0100327,"hypercholanemia, familial","['hypercholanemia, familial', 'familial hypercholanemia']",,,,,,,,,,,,
mondo:0100328,"microcephaly, epilepsy, and diabetes syndrome",,,,,,,,,,,,,
mondo:0100329,primary viral infectious disease,,,,,,,,,,,,,
mondo:0100330,disease arising from reactivation of latent virus,['latent infection'],,,,,,,,,,,,
mondo:0100331,nerve agent poisoning,,,,,,,,,,,,,
mondo:0100335,local anesthetic poisoning,['local anesthetic poisoning'],,,,,,,,,,,,
mondo:0100337,SEC61A1 deficiency,,,,,,,,,,,,,
mondo:0100338,urinary tract infection,['urinary tract infection (disease)'],0080784,,,,,,,D014552,,,,
mondo:0100339,Friedreich ataxia,"['Friedreich^s tabes', 'Friedreich ataxia with retained reflexes', 'hereditary spinal sclerosis', 'Friedreich^s ataxia', 'spinocerebellar ataxia, Friedreich', 'hereditary spinal ataxia', 'FA', 'FRDA', 'Friedreich ataxia']",12705,,,C0016719,,C84718,,D005621,334.0,,10017374,
mondo:0100340,Friedreich ataxia 1,"['FRDA1', 'Friedreich ataxia type 1', 'Friedreich ataxia', 'Friedreich ataxia 1']",0111218,229300,95,C1856689,"['0.2207', '0.472', '-0.1455', '-0.377', '-0.2156', '-0.4485', '0.5513', '0.78', '-0.5454', '-0.3313', '-0.11224', '-0.4304', '-0.095', '0.2289', '0.221', '-0.1409', '-0.2705', '-0.613', '0.1644', '-0.1464', '0.31', '-0.03745', '-0.1611', '-0.04166', '0.09796', '-0.187', '0.1448', '-0.216', '0.082', '0.00789', '0.64', '0.01186', '-0.1943', '0.003765', '-0.423', '-0.3843', '0.1555', '-0.5674', '-0.4211', '-0.1125', '-0.2422', '0.1237', '0.5957', '0.695', '0.04193', '-0.1627', '0.01036', '0.4177', '0.1421', '-0.1216', '-0.1247', '0.2527', '-0.0281', '-0.1937', '0.6655', '-0.2201', '0.4836', '0.0828', '-0.4392', '0.0753', '0.5483', '0.2805', '-0.1302', '0.2375', '-0.891', '0.235', '0.1781', '0.1985', '-0.10297', '0.4485', '0.04416', '-0.2135', '-0.43', '-0.3987', '0.617', '0.1509', '0.09375', '-0.313', '-0.3188', '-0.61', '0.0889', '-0.6963', '0.02167', '0.682', '-0.2019', '0.6577', '-0.0618', '-0.552', '0.6816', '0.1602', '0.43', '-0.2225', '-0.1322', '0.4797', '0.417', '-0.05304', '0.7114', '0.1315', '-0.1613', '-0.11505']",,,C565561,,,,
mondo:0100341,fire ant poisoning,"['fire ant allergy', 'fire ant sting', 'fire ant bite']",,,,,,,,,,,,
mondo:0100342,malignant glioma,"['malignant glial tumor', 'malignant glial neoplasm', 'malignant neuroglial tumour', 'neuroglial tumor', 'glial cell tumour', 'high-grade glioma', 'malignant neuroglial tumor', 'malignant neuroglial neoplasm', 'neuroglial tumour', 'glial cell tumor', 'high grade glioma', 'malignant glial tumour', 'glioma, malignant', 'malignant glioma', 'glioma']",3070,,,C0555198,,C4822,,,,,10018338,
mondo:0100343,antenatal Bartter syndrome,"['Bartter syndrome, furosemide-amiloride type', 'Bartter syndrome, furosemide type', 'hyperprostaglandin E syndrome']",,,93604,,,,,,,,,
mondo:0100344,Bartter disease type 1,"['antenatal Bartter syndrome type 1', 'hyperprostaglandin E syndrome', 'Bartter syndrome, antenatal, type 1', 'SLC12A1 Bartter syndrome', 'Bartter syndrome, furosemide-amiloride type', 'Bartter syndrome, type 1, antenatal', 'Bartter syndrome antenatal type 1', 'BARTS1', 'Bartter syndrome type 1 antenatal', 'hypokalemic alkalosis with hypercalciuria antenatal 1', 'hypokalemic alkalosis with hypercalciuria 1, antenatal', 'hypokalemic alkalosis with hypercalciuria 1 antenatal', 'hypokalemic alkalosis with hypercalciuria, antenatal, 1', 'Bartter disease type 1', 'Bartter syndrome, furosemide type', 'Bartter syndrome, type 1', 'antenatal Bartter syndrome', 'Bartter syndrome caused by mutation in SLC12A1', 'hyperprostaglandin E syndrome 1', 'Bartter syndrome type 1']",0110142,601678,620217,,,,,C537652,,,,
mondo:0100345,lactose intolerance,"['LM - lactose malabsorption', 'lactose intolerance (disease)', 'lactose intolerance', 'lactase persistence']",10604,,,C0022951,"['0.2769', '0.414', '0.03036', '0.588', '-0.4666', '0.03174', '-0.2108', '0.3364', '-0.2812', '-0.03775', '0.2156', '0.1757', '-0.2141', '0.6157', '-0.4124', '-0.2537', '-0.407', '0.1749', '-0.2908', '-0.4604', '0.0909', '-0.2957', '-0.3806', '0.04297', '0.2087', '-0.4033', '-0.334', '-0.342', '0.4536', '-0.4067', '-0.0933', '-0.556', '0.1979', '0.01657', '0.301', '0.10266', '-0.02783', '0.3215', '0.6294', '-0.01688', '-0.1754', '-0.2499', '0.2421', '-0.1112', '-0.0903', '-0.419', '-0.1486', '0.317', '0.1849', '0.4216', '-0.2147', '-0.1109', '0.357', '0.2059', '0.1498', '0.1026', '-0.2593', '0.011024', '-0.3838', '-0.2041', '0.3398', '0.3884', '0.1771', '-0.1492', '0.2554', '0.1395', '0.3079', '0.3225', '-0.2769', '0.1472', '0.128', '0.4485', '-0.0788', '-0.8633', '0.3125', '0.634', '-0.3586', '0.0966', '0.0427', '0.259', '-0.3406', '-0.2783', '-0.1109', '-0.05948', '0.02429', '0.2382', '0.0361', '-0.3247', '1.1', '-0.03326', '0.01584', '0.01061', '-0.534', '0.119', '0.6426', '0.4138', '-0.2861', '-0.52', '-0.5923', '-0.06058']",C3154,1000062,D007787,271.3,,,0004789
mondo:0100346,microcephaly with or without short stature,,,,,,,,,,,,,
mondo:0100347,carcinoid syndrome,"['carcinoid tumor syndrome', 'carcinoid syndrome', 'carcinoid tumour syndrome', 'malignant carcinoid syndrome', 'carcinoid tumors, intestinal']",,,100093,,,C3215,1000852,,259.2,E34.0,10007270,
mondo:0100348,"neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities","['neurodevelopmental disorder with microcephaly, impaired language, and gait abnormalities, autosomal recessive', 'NEDMILG, AR']",,619091,,,,,,,,,,
mondo:0100349,COACH syndrome,"['cerebellar vermis hypoplasia-oligophrenia-congenital ataxia-coloboma-hepatic fibrosis', 'cerebellar vermis hypo/aplasia, oligophrenia, ataxia congenital, coloboma, and hepatic fibrosis', 'gentile syndrome', 'Joubert syndrome with hepatic defect', 'JS-H', 'Joubert syndrome with congenital hepatic fibrosis']",0111589,,1454,C1857662,"['-0.153', '0.1443', '-0.42', '0.1575', '-0.2363', '0.005226', '-0.1847', '0.2461', '-0.2795', '-0.3418', '-0.2744', '-0.706', '-0.5947', '-0.03534', '0.1947', '-0.6533', '0.252', '0.04852', '0.005882', '-1.628', '0.0285', '0.0971', '0.4976', '0.1043', '0.2472', '0.4924', '-0.5854', '0.559', '0.592', '-0.3623', '0.611', '0.0877', '0.495', '0.3552', '0.3743', '-0.532', '-0.2988', '-0.4717', '-0.1965', '0.1865', '0.231', '-0.1449', '0.1422', '0.4058', '0.1873', '-0.265', '0.3462', '0.1823', '0.2593', '0.1903', '0.2094', '0.1754', '-0.5366', '-0.275', '-0.7803', '-0.05032', '0.603', '-0.0571', '-0.2097', '0.2834', '0.4443', '-0.2795', '0.495', '0.10925', '-0.1744', '-0.2222', '0.1051', '0.655', '-0.588', '0.4988', '-0.1904', '-0.02272', '0.4807', '0.4875', '0.7896', '-0.1992', '0.4492', '-0.4377', '-0.2612', '-0.12', '0.317', '-0.0933', '0.01467', '0.2507', '-0.1674', '-0.2295', '0.8955', '0.4631', '0.3677', '0.2463', '0.287', '0.1631', '0.11835', '-0.268', '0.3088', '0.0733', '0.764', '-0.1462', '-0.3176', '0.2188']",,,C536430,,,,
mondo:0100350,"neuronopathy, distal hereditary motor, type 5","['distal spinal muscular atrophy type 5', 'dHMN5', 'distal hereditary motor neuropathy type V', 'distal HMN V']",0111203,,139536,,"['-0.01457', '0.09357', '0.06174', '0.00728', '0.02441', '-0.1503', '-0.0688', '0.1868', '-0.2064', '0.06915', '-0.0347', '0.04675', '-0.02766', '0.01817', '0.014824', '-0.08746', '-0.01749', '-0.0667', '0.01773', '-0.2607', '0.02315', '-0.08075', '0.074', '0.06757', '0.02086', '0.01074', '-0.01738', '-0.03812', '-0.0683', '-0.09863', '0.0877', '-0.002396', '0.1198', '0.02206', '0.02504', '-0.1392', '-0.02994', '-0.0981', '-0.04233', '-0.1028', '-0.001137', '-0.203', '0.01026', '0.0728', '-0.0225', '-0.1519', '-0.07263', '0.1301', '0.02776', '0.0357', '-0.04294', '0.02003', '-0.0556', '-0.03583', '-0.03001', '-0.0842', '0.1503', '-0.07184', '-0.1282', '0.01485', '0.06287', '0.00098', '0.12463', '0.0649', '-0.03754', '0.07587', '0.1361', '0.2451', '-0.1277', '0.1486', '-0.0815', '-0.004276', '0.02104', '-0.1643', '0.2034', '0.1191', '-0.06775', '0.0427', '-0.1091', '-0.09265', '-0.03232', '-0.04596', '-0.01924', '0.1696', '-0.0919', '0.001834', '-0.003654', '0.1361', '0.11395', '-0.02081', '0.1101', '0.0985', '0.0939', '-0.00648', '0.2693', '0.09595', '0.1453', '-0.1387', '-0.0562', '0.0444']",,,C563443,,,,
mondo:0100351,POLD1-related polyposis and colorectal cancer syndrome,,,,,,,,,,,,,
mondo:0100352,episodic kinesigenic dyskinesia 1,"['paroxysmal kinesigenic dyskinesia', 'EKD1', 'dystonia, familial paroxysmal', 'episodic kinesigenic dyskinesia type 1', 'paroxysmal kinesigenic choreoathetosis', 'DYT-PRRT2', 'episodic kinesigenic dyskinesia caused by mutation in PRRT2', 'PRRT2 episodic kinesigenic dyskinesia', 'episodic kinesigenic dyskinesia 1', 'PxMD-PRRT2', 'dystonia 10']",0090053,128200,,,,,,C537180,333.5,,,
mondo:0100353,HHV-7 infectious disease,"['HHV-7 infection', 'herpesvirus-7 infectious disease']",,,,,,,,,,,,
mondo:0100354,megacystis-microcolon-intestinal hypoperistalsis syndrome 1,"['megacystis, microcolon, hypoperistalsis syndrome', 'megacystis-microcolon-intestinal hypoperistalsis syndrome', 'MMIHS', 'megacystis microcolon intestinal hypoperistalsis syndrome', 'megacystis-microcolon-intestinal hypoperistalsis-hydronephrosis syndrome', 'megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH', 'Berdon syndrome', 'megacystis, microcolon, intestinal hypoperistalsis syndrome', 'MMIH syndrome']",0060610,249210,2241,C1864996,"['-0.04373', '0.03574', '0.012276', '-0.02426', '0.004066', '-0.0768', '-0.002733', '0.05804', '-0.06198', '-0.03833', '-0.01252', '-0.01227', '-0.006798', '0.01569', '-0.03827', '-0.05753', '0.0006976', '-0.00718', '-0.02411', '-0.11487', '-0.00927', '-0.02151', '0.05356', '-0.0188', '0.03345', '-0.005016', '-0.02028', '-0.00657', '0.0501', '-0.03494', '0.03802', '-0.009636', '0.05765', '0.03796', '0.03044', '-0.01613', '-0.01155', '-0.03122', '0.007507', '-0.07043', '0.018', '-0.04062', '0.0216', '-0.03625', '-0.00376', '-0.06305', '-0.02695', '0.0623', '0.02026', '0.01301', '-0.01826', '0.002558', '0.00376', '0.002424', '-0.0552', '-0.02292', '0.04883', '-0.01573', '-0.06287', '-0.01405', '0.04376', '0.04565', '-0.003426', '-0.003796', '-0.00256', '0.01869', '0.067', '0.03214', '-0.071', '0.08826', '-0.0695', '0.00343', '0.02252', '-0.05975', '0.006653', '0.0035', '-0.002708', '-0.007076', '-0.05292', '-0.03247', '0.001244', '0.000136', '-0.02364', '0.05554', '-0.008125', '0.012726', '0.03485', '0.072', '0.0797', '-0.01069', '0.0166', '0.0415', '0.019', '0.02652', '0.145', '0.008896', '0.072', '-0.0966', '-0.02594', '0.03918']",C98982,,C536138,,,,
mondo:0100355,classic or non-classic genetic disease presentation,,,,,,,,,,,,,
mondo:0100356,classic presentation,,,,,,,,,,,,,
mondo:0100357,non-classic presentation,,,,,,,,,,,,,
mondo:0100358,ectodermal dysplasia WNT10A related,['ectodermal dysplasia WNT10A related'],,,,,,,,,,,,
mondo:0100359,herpes simplex type 1 infectious disease,,,,,,,,,,,,,
mondo:0100360,herpes simplex type 2 infectious disease,,,,,,,,,,,,,
mondo:0100361,lip herpes simplex type 1 infectious disorder,,,,,,,,,,,,,
mondo:0100362,lip herpes simplex type 2 infectious disorder,,,,,,,,,,,,,
mondo:0100363,genital herpes simplex type 2 infectious disorder,,,,,,,,,,,,,
mondo:0100364,genital herpes simplex type 1 infectious disorder,,,,,,,,,,,,,
mondo:0100365,mucopolysaccharidosis or mucopolysaccharidosis-like disorder,,,,,,,,,,,,,
mondo:0100366,occupational disorder,,,,,,,,,,,,,
mondo:0100367,port-wine nevi-mega cisterna magna-hydrocephalus syndrome,['nova syndrome'],,,2703,,,,,,,,,
mondo:0100368,RPE65-related recessive retinopathy,"['retinitis pigmentosa 20', 'RPE65 Leber congenital amaurosis', 'amaurosis congenita of Leber II', 'RPE65 retinitis pigmentosa', 'Leber congenital amaurosis 2', 'LCA2', 'retinitis pigmentosa caused by mutation in RPE65', 'RP20', 'recessive RPE65 retinopathy', 'Leber congenital amaurosis type 2', 'amaurosis congenita of Leber 2', 'amaurosis congenita of Leber, type 2', 'Leber congenital amaurosis caused by mutation in RPE65']",,,,,,,,,,,,
mondo:0100369,iatrogenic or non-iatrogenic,,,,,,,,,,,,,
mondo:0100370,acute hepatitis B virus infection,['acute hepatitis B'],,,,,,C157781,,,,,,
mondo:0100371,acute hepatitis C virus infection,['acute hepatitis C'],,,,,,C157782,,,,,,
mondo:0100372,disorder of peroxisomal transporter,['disorder of peroxisomal transporter defect'],,,,,,,,,,,,
mondo:0100373,"acute myeloid leukemia, inv(16)(p13.1;q22)","['AML, inv(16)(p13;q22)', 'AML, inv(16)(p13q22)', 'AML, inv(16)(p13.1q22.1)', 'AML, inv(16)(p13.1;q22.1)', 'AML, inv(16)(p13.1;q22)', 'AML, inv(16)(p13.1q22)']",,,,,,C9018,,,,,,
mondo:0100374,"acute myeloid leukemia, t(16;16)(p13.1;q22)","['AML, t(16;16)(p13.1;q22)', 'AML, t(16;16)(p13.1;q22.1)', 'AML, t(16;16)(p13.1q22)', 'AML, t(16;16)(p13;q22)', 'AML, t(16;16)(p13q22)', 'AML, t(16;16)(p13.1q22.1)']",,,,,,C9019,,,,,,
mondo:0100375,"acute myeloid leukemia, t(15;17)(q24;q21)","['AML, t(15;17)(q24;q21)', 'AML, t(15;17)(q22;q12)', 'AML, t(15;17)(q22;q21)']",,,,,,C36055,,,,,,
mondo:0100376,"acute myeloid leukemia, t(9;11)(p21.3;q23.3)","['AML, t(9;11)(p21.3;q23.3)', 'AML, t(9;11)(p22;q23)']",,,,,,,,,,,,
mondo:0100377,"acute myeloid leukemia, t(10;11)(p12;q23)","['AML, t(10;11)(p12;q23)']",,,,,,C132101,,,,,,
mondo:0100378,"acute myeloid leukemia, t(10;11)(p11.2;q23)","['AML, t(10;11)(p11.2;q23)']",,,,,,,,,,,,
mondo:0100379,"acute myeloid leukemia, t(1;11)(q21;q23)","['AML, t(1;11)(q21;q23)']",,,,,,,,,,,,
mondo:0100380,"acute myeloid leukemia, t(4;11)(q21;q23)","['AML, t(4;11)(q21;q23.3)', 'AML, t(4;11)(q21;q23)']",,,,,,,,,,,,
mondo:0100381,"acute myeloid leukemia, t(6;11)(q27;q23)","['AML, t(6;11)(q27;q23.3)', 'AML, t(6;11)(q27;q23)']",,,,,,C132105,,,,,,
mondo:0100382,"acute myeloid leukemia, t(6;9)(p23;q34.1)","['AML, t(6;9)(p23;q34)', 'AML, t(6;9)(p23;q34.1)', 'AML, t(6;9)(p22;q34)', 'AML, t(6;9)(p22.3;q34.1)']",0081080,,,,,C82423,,,,,,
mondo:0100383,"acute myeloid leukemia, t(11;19)(q23;p13)","['AML, t(11;19)(q23;p13)']",,,,,,,,,,,,
mondo:0100384,"acute myeloid leukemia, t(11;19)(q23;p13.1)","['AML, t(11;19)(q23;p13.1)']",,,,,,,,,,,,
mondo:0100385,"acute myeloid leukemia, t(11;19)(q23.3;p13.3)","['AML, t(11;19)(q23.3;p13.3)', 'AML, t(11;19)(q23;p13.3)']",,,,,,,,,,,,
mondo:0100386,"acute myeloid leukemia, t(v;11q23.3)","['AML, t(V;11)(v;q23.3)', 'AML, t(11;v)(q23.3;v)', 'AML, t(11;v)(q23;v)', 'AML, 11q23.3 Translocation', 'AML, t(v;11q23.3)', 'AML, t(V;11)(v;q23)']",,,,,,,,,,,,
mondo:0100387,"acute myeloid leukemia, Monosomy 7","['AML, Monosomy 7']",,,,,,,,,,,,
mondo:0100388,"acute myeloid leukemia, Monosomy 5","['AML, Monosomy 5']",,,,,,,,,,,,
mondo:0100389,"acute myeloid leukemia, Trisomy 8","['AML, Trisomy 8', 'AML, tri8']",,,,,,C162775,,,,,,
mondo:0100390,"acute myeloid leukemia, der12p","['AML, der(12p)', 'AML, der12p']",,,,,,,,,,,,
mondo:0100391,"acute myeloid leukemia, t(2;12)","['AML, t(2;12)']",,,,,,,,,,,,
mondo:0100392,"acute myeloid leukemia, t(11;17)","['AML, t(11;17)']",,,,,,,,,,,,
mondo:0100393,"acute myeloid leukemia, t(8;16)","['AML, t(8;16)']",,,,,,,,,,,,
mondo:0100394,"acute myeloid leukemia, t(1;22)","['AML, t(1;22)']",,,,,,,,,,,,
mondo:0100395,"acute myeloid leukemia, t(5;11)(q35;p15)","['AML, t(5;11)(q35;p15)']",,,,,,C131502,,,,,,
mondo:0100396,"acute myeloid leukemia, t(7;12)(q36;p13)","['AML, t(7;12)(q36;p13)']",,,,,,C122690,,,,,,
mondo:0100397,"acute myeloid leukemia, t(9;22)(q34.1;q11.2)","['AML, t(9;22)(q34;q11)', 'AML, t(9;22)(q34.1;q11.2)', 'AML, t(9;22)(q34;q11.2)']",,,,,,,,,,,,
mondo:0100398,"acute myeloid leukemia, inv(3)(q21.3;q26.2)","['AML, inv(3)(q21q26.2)', 'AML, inv(3)(q21.3;q26.2)', 'AML, inv(3)(q21.3q26.2)']",,,,,,C122716,,,,,,
mondo:0100399,"acute myeloid leukemia, t(3;3)(q21.3;q26.2)","['AML, t(3;3)(q26;q21)', 'AML, t(3;3)(q21;q26.2)', 'AML, t(3;3)(q21.3q26.2)', 'AML, t(3;3)(q21.3;q26.2)']",,,,,,C122717,,,,,,
mondo:0100400,"acute myeloid leukemia, t(3;12)(q23;p12.3)","['AML, t(3;12)(q23;p12.3)']",,,,,,,,,,,,
mondo:0100401,"acute myeloid leukemia, del(5q31-q32)","['AML, del(5)(q31q32)', 'AML, del(5q31-q32)', 'AML, 5q31-32 Deletion', 'AML, del(5)(q31-q32)']",,,,,,,,,,,,
mondo:0100402,"acute myeloid leukemia, del(13q14-q21)","['AML, del(13)(q14-q21)', 'AML, del(13q14-q21)', 'AML, del(13q)(13q14-21)', 'AML, 13q14-q21 Deletion', 'AML, del(13)(q14q21)']",,,,,,,,,,,,
mondo:0100403,"acute myeloid leukemia, loss of chromosome 17p","['AML, del(17p)', 'AML, loss of chromosome 17p']",,,,,,,,,,,,
mondo:0100404,"acute myeloid leukemia, MLL gene rearrangement","['AML, KMT2A Rearrangement', 'AML, Myeloid/Lymphoid or Mixed Lineage Leukaemia Gene Rearrangement', 'AML, Myeloid/Lymphoid Leukemia Gene Rearrangement', 'AML, MLL gene rearrangement', 'AML, Myeloid/Lymphoid or Mixed-Lineage Leukaemia (Trithorax Homolog, Drosophila) Gene Rearrangement', 'AML, Myeloid/Lymphoid or Mixed Lineage Leukemia Gene Rearrangement', 'AML, Mixed Lineage Leukaemia Gene Rearrangement', 'AML, Lysine Methyltransferase 2A Gene Rearrangement', 'AML, Mixed Lineage Leukemia Gene Rearrangement', 'AML, KMT2A Gene Rearrangement', 'AML, Myeloid/Lymphoid Leukaemia Gene Rearrangement', 'AML, Lysine (K)-Specific Methyltransferase 2A Gene Rearrangement', 'AML, Myeloid/Lymphoid or Mixed-Lineage Leukemia (Trithorax Homolog, Drosophila) Gene Rearrangement', 'AML, MLL Rearrangement']",0081094,,,,,C174129,,,,,,
mondo:0100405,"acute myeloid leukemia, Non-KMT2A MLLT10 rearrangement positive","['AML, Non-MLL MLLT10 Rearrangement Positive', 'AML, Non-KMT2A MLLT10 rearrangement positive', 'AML, Non-MLL MLLT10 Rearrangement', 'AML, Non-KMT2A MLLT10 Rearrangement']",,,,,,,,,,,,
mondo:0100406,"acute myeloid leukemia, inv(16)(p13.3;q24.3)","['AML, inv(16)(p13.3;q24.3)', 'AML, inv(16)(p13.3q24.3)', 'AML, inv(16)(p13;q24)', 'AML, inv(16)(p13q24)']",,,,,,,,,,,,
mondo:0100407,"acute myeloid leukemia, t(11;15)(p15;q35)","['AML, t(11;15)(p15;q35)']",,,,,,C131504,,,,,,
mondo:0100408,"acute myeloid leukemia, t(16;21)(q24;q22)","['AML, t(16;21)(q24;q22)']",,,,,,,,,,,,
mondo:0100409,"acute myeloid leukemia, t(3;5)(q25;q34)","['AML, t(3;5)(q25;q34)']",0081092,,,,,C7600,,,,,,
mondo:0100410,"acute myeloid leukemia, t(16;21)(p11;q22)","['AML, t(16;21)(p11.2;q22.2)', 'AML, t(16;21)(p11;q22)']",,,,,,,,,,,,
mondo:0100412,"acute myeloid leukemia, monoallelic CEBPA gene mutation","['AML, CEBPA Monoallelic Gene Mutation', 'AML, CCAAT/Enhancer Binding Protein Alpha Monoallelic Gene Mutation', 'AML, CCAAT/Enhancer Binding Protein, Alpha Monoallelic Gene Mutation', 'AML, CCAAT Enhancer Binding Protein Alpha Monoallelic Gene Mutation', 'AML, monoallelic CEBPA gene mutation', 'AML, CEBPA Monoallelic Mutation', 'AML, moCEBPA', 'AML, CEBP Monoallelic Gene Mutation', 'AML, C/EBP-Alpha Monoallelic Gene Mutation', 'AML, C/EBPalpha Monoallelic Gene Mutation']",,,,,,,,,,,,
mondo:0100413,"acute myeloid leukemia, biallelic CEBPA gene mutation","['AML, biCEBPA', 'AML, C/EBP-Alpha Biallelic Gene Mutation', 'AML, CCAAT/Enhancer Binding Protein, Alpha Biallelic Gene Mutation', 'AML, C/EBPalpha Biallelic Gene Mutation', 'AML, biallelic CEBPA gene mutation', 'AML, CEBPA Biallelic Gene Mutation', 'AML, CEBP Biallelic Gene Mutation', 'AML, CEBPA Biallelic Mutation', 'AML, CCAAT/Enhancer Binding Protein Alpha Biallelic Gene Mutation', 'AML, CCAAT Enhancer Binding Protein Alpha Biallelic Gene Mutation']",0081090,,,,,,,,,,,
mondo:0100414,"acute myeloid leukemia, CEBPA gene mutation","['AML, CEBPA Mutation', 'AML, C/EBPalpha Mutation', 'AML, CCAAT Enhancer Binding Protein Alpha Gene Mutation', 'AML, C/EBP-Alpha Gene Mutation', 'AML, CEBP Gene Mutation', 'AML, CEBPA gene mutation', 'AML, CCAAT/Enhancer Binding Protein, Alpha Gene Mutation']",,,,,,C151898,,,,,,
mondo:0100415,"acute myeloid leukemia, FLT3 internal tandem duplication","['AML, FLT3-ITD Mutation', 'AML, FLT3-ITD', 'AML, FLT3/ITD Mutation', 'AML, FLT3-ITD Activating Mutation', 'AML, Activating FLT3-ITD Gene Mutation', 'AML, FLT3 internal tandem duplication', 'AML, Activating FLT3-ITD Mutation', 'AML, FLT3 ITD']",,,,,,C126748,,,,,,
mondo:0100416,"acute myeloid leukemia, FLT3 tyrosine kinase domain point mutation","['AML, FLT3 tyrosine kinase domain point mutation', 'AML, FLT3-TKD Point Mutation', 'AML, FLT3/TKD Point Mutation']",,,,,,,,,,,,
mondo:0100417,"acute myeloid leukemia, WT1 gene mutation","['AML, GUD Gene Mutation', 'AML, WT1 mutation', 'AML, Wilms Tumor 1 Gene Mutation', 'AML, WT33 Gene Mutation', 'AML, Wilms Tumour 1 Gene Mutation', 'AML, WT1 gene mutation', 'AML, WAGR Gene Mutation', 'AML, WIT-2 Gene Mutation']",,,,,,,,,,,,
mondo:0100418,"acute myeloid leukemia, KIT exon 17 mutation","['AML, c-KIT Exon 17 Mutation', 'AML, KIT exon 17 mutation', 'AML, CD117 Exon 17 Mutation', 'AML, KIT Proto-Oncogene Tyrosine Protein Kinase Gene Exon 17 Mutation', 'AML, v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Exon 17 Mutation']",,,,,,,,,,,,
mondo:0100419,"acute myeloid leukemia, KIT exon 8 mutation","['AML, KIT Proto-Oncogene Tyrosine Protein Kinase Gene Exon 8 Mutation', 'AML, KIT exon 8 mutation', 'AML, CD117 Exon 8 Mutation', 'AML, v-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Exon 8 Mutation', 'AML, c-KIT Exon 8 Mutation']",,,,,,,,,,,,
mondo:0100420,"acute myeloid leukemia, KIT gene mutation","['AML, KIT gene mutation', 'AML, c-KIT Gene Mutation', 'AML, CD117 Gene Mutation', 'AML, CD117 Mutation', 'AML, C-KIT Mutation', 'AML, KIT Proto-Oncogene Tyrosine Protein Kinase Gene Mutation', 'AML, V-Kit Hardy-Zuckerman 4 Feline Sarcoma Viral Oncogene Homolog Gene Mutation']",,,,,,,,,,,,
mondo:0100421,"acute myeloid leukemia, GATA1 gene mutation","['AML, GF-1 Gene Mutation', 'AML, GATA Binding Protein 1 Gene Mutation', 'AML, ERYF1 Gene Mutation', 'AML, NFE1 Gene Mutation', 'AML, NF-E1 Gene Mutation', 'AML, GATA1 Mutation', 'AML, GF1 Gene Mutation', 'AML, GATA1 gene mutation', 'AML, GATA-1 Gene Mutation']",,,,,,,,,,,,
mondo:0100422,"acute myeloid leukemia, RUNX1 gene mutation","['AML, CBFA2 Gene Mutation', 'AML, Acute Myeloid Leukaemia 1 Gene Mutation', 'AML, AML1 Mutation', 'AML, Acute Myeloid Leukemia 1 Gene Mutation', 'AML, RUNX1 gene mutation', 'AML, AMLCR1 Gene Mutation', 'AML, CBFalpha2 Mutation', 'AML, Runt-Related Transcription Factor 1 Gene Mutation', 'AML, AML1 Gene Mutation']",0081091,,,,,C129786,,,,,,
mondo:0100423,"acute myeloid leukemia, PTPN11 gene mutation","['AML, BPTP3 Gene Mutation', 'AML, PTPN11 gene mutation', 'AML, Protein Tyrosine Phosphatase Non-Receptor Type 11 Gene Mutation', 'AML, Protein Tyrosine Phosphatase, Non-Receptor Type 11 Gene Mutation', 'AML, SHP-2 Gene Mutation', 'AML, PTP2C Gene Mutation', 'AML, SHP2 Gene Mutation', 'AML, SH-PTP2 Gene Mutation', 'AML, PTP-1D Gene Mutation']",,,,,,,,,,,,
mondo:0100424,"acute myeloid leukemia, NRAS gene mutation","['AML, Neuroblastoma RAS Viral Oncogene Homolog Gene Mutation', 'AML, N-RAS Gene Mutation', 'AML, NRAS gene mutation']",,,,,,,,,,,,
mondo:0100425,"acute myeloid leukemia, KRAS gene mutation","['AML, c-K-ras Gene Mutation', 'AML, v-Ki-ras2 Kirsten Rat Sarcoma Viral Oncogene Homolog Gene Mutation', 'AML, KRAS gene mutation', 'AML, KRAS2 Gene Mutation', 'AML, KRAS-2 Gene Mutation', 'AML, KRAS Gene Mutation']",,,,,,,,,,,,
mondo:0100426,iatrogenic,,,,,,,,,,,,,
mondo:0100427,non-iatrogenic,,,,,,,,,,,,,
mondo:0100428,progressive bulbar palsy of childhood,['Fazio-Londe disease'],0080632,211500,56965,C0393540,,,,,,,,
mondo:0100429,intrahepatic cholestasis of pregnancy,"['cholestasis, intrahepatic of pregnancy', 'pregnancy related cholestasis', 'RICP', 'gravidic intrahepatic cholestasis', 'familial recurrent intrahepatic cholestasis of pregnancy', 'ICP', 'intrahepatic cholestasis of pregnancy', 'recurrent intrahepatic cholestasis of pregnancy', 'familial intrahepatic cholestasis of pregnancy', 'pregnancy-related cholestasis']",0070227,,69665,,,,0009048,C535932,,,,
mondo:0100430,fibrotic liver disease,"['hepatic fibrosis (disease)', 'liver fibrosis (disease)']",,,,,,,,,,,,
mondo:0100431,migraine without aura,['common migraine'],12783,,,C0338480,,C117004,0005296,D020326,,,,
mondo:0100432,FNIP1-associated syndrome,"['absent B cells, agammaglobulinemia, and hypertrophic cardiomyopathy syndrome', 'immunodeficiency with cardiomyopathy and pre-excitation syndrome', 'FNIP1 deficiency']",,,,,,,,,,,,
mondo:0100433,ACTB-associated syndromic thrombocytopenia,['ACTB-AST'],,,,,,,,,,,,
mondo:0100434,chronic mountain sickness,['Monge^s disease'],,,,,,,0010143,,,,,
mondo:0100435,Schwartz-Jampel syndrome type 1,"['Schwartz-Jampel syndrome 1', 'Chondrodystrophic myotonia', 'SJS1', 'Schwartz-Jampel syndrome, type 1', 'Schwartz-Jampel syndrome type 1', 'SJA syndrome']",0090005,255800,,,,,,,,,,
mondo:0100436,"cataract 2, multiple types","['CTRCT2', 'cataract, Coppock-like', 'cataract 2 multiple types with or without microcornea', 'cataract 2 multiple types', 'cataract 2, multiple types, with or without microcornea']",0110235,604307,,,,,,,,,,
mondo:0100437,RPGR-related retinopathy,"['macular degeneration, X-linked atrophic', 'RP3', 'RPGR retinopathy', 'cone dystrophy 1, X-linked', 'cone-rod degeneration, X-linked', 'COD1', 'retinitis pigmentosa caused by mutation in RPGR', 'X-linked cone-rod dystrophy type 1', 'retinitis pigmentosa 15', 'cone-rod dystrophy, X-linked, 1', 'X-linked cone dystrophy 1', 'CORDX1', 'cone-rod dystrophy X-linked 1', 'cone dystrophy X-linked 1', 'RPGR retinitis pigmentosa', 'retinitis pigmentosa 3', 'choroidoretinal degeneration with retinal reflex in heterozygous women', 'retinal ciliopathy due to mutation in the RPGR gene', 'retinitis pigmentosa type 3', 'X-linked cone-rod dystrophy 1', 'cone-rod dystrophy, X-linked, type 1']",,,,,,,,,,,,
mondo:0100438,AIPL1-related retinopathy,"['cone-rod dystrophy', 'Leber congenital amaurosis 4', 'LCA4', 'Leber congenital amaurosis type 4', 'retinitis pigmentosa, juvenile, AIPL1-related', 'AIPL1 retinopathy', 'Leber congenital amaurosis caused by mutation in AIPL1', 'retinitis pigmentosa, juvenile', 'amaurosis congenita of Leber, type 4', 'cone-rod dystrophy, AIPL1-related', 'AIPL1 Leber congenital amaurosis']",,,,,,,,,,,,
mondo:0100439,glycogen storage disease IXa2,"['liver glycogenosis, X-linked, type 2', 'GSD IXa2', 'GSD9A2']",,,,,,,,,,,,
mondo:0100440,"Asperger syndrome, susceptibility to",,,,,,,,,,,,,
mondo:0100441,GUCY2D-related dominant retinopathy,"['cone-rod dystrophy type 6', 'CORD6', 'choroidal dystrophy, central areolar', 'choroidal sclerosis', 'retinal cone dystrophy 2', 'GUCY2D cone-rod dystrophy', 'cone-rod dystrophy 6', 'RCD2', 'dominant GUCY2D retinopathy', 'choroidal dystrophy, central areolar, 1', 'CACD1', 'central areolar choroidal dystrophy caused by mutation in GUCY2D', 'GUCY2D central areolar choroidal dystrophy', 'cone-rod dystrophy caused by mutation in GUCY2D']",,,,,,,,,,,,
mondo:0100442,RP2-related retinopathy,"['RP2 retinopathy', 'retinitis pigmentosa 2', 'RP2', 'RP2 retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in RP2', 'retinitis pigmentosa type 2']",,,,,,,,,,,,
mondo:0100443,RDH5-related retinopathy,"['fundus albipunctatus', 'RDH5 retinopathy', 'pigmentary retinal dystrophy', 'retinitis punctata albescens']",,,,,,,,,,,,
mondo:0100444,RLBP1-related retinopathy,"['fundus albipunctatus', 'NFRCD', 'Newfoundland rod-cone dystrophy', 'RLBP1 retinopathy', 'retinitis punctata albescens', 'RLBP1 cone-rod dystrophy', 'Vasterbotten dystrophy', 'cone-rod dystrophy caused by mutation in RLBP1', 'Newfoundland ROD-cone dystrophy', 'Bothnia retinal dystrophy', 'Västerbotten dystrophy', 'pigmentary retinal dystrophy']",,,,,,,,,,,,
mondo:0100445,LCA5-related retinopathy,"['Leber congenital amaurosis caused by mutation in LCA5', 'LCA5', 'Leber congenital amaurosis type 5', 'LCA5 Leber congenital amaurosis', 'Leber congenital amaurosis 5', 'amaurosis congenita of Leber, type 5', 'LCA5 retinopathy']",,,,,,,,,,,,
mondo:0100446,CNGB3-related retinopathy,"['ACHM1', 'achromatopsia type 3', 'CNGB3 retinopathy', 'rod monochromatism 1, formerly', 'Rod monochromatism 1 (formerly)', 'ACHM1, formerly', 'RMCH1', 'rod monochromacy 1', 'ACHM1 (formerly)', 'ACHM3', 'total colorblindness with myopia', 'rod monochromatism 1', 'achromatopsia 3', 'RMCH1 (formerly)', 'CNGB3 achromatopsia', 'Rod monochromacy 1 (formerly)', 'achromatopsia caused by mutation in CNGB3', 'achromatopsia with myopia', 'rod monochromacy 1, formerly']",,,,,,,,,,,,
mondo:0100447,ATF6-related retinopathy,"['achromatopsia type 7', 'ATF6 retinopathy', 'ACHM7', 'achromatopsia 7', 'ATF6 achromatopsia', 'achromatopsia caused by mutation in ATF6']",,,,,,,,,,,,
mondo:0100448,RAB28-related retinopathy,"['CORD18', 'cone-rod dystrophy type 18', 'RAB28 retinopathy', 'cone-rod dystrophy 18', 'cone-rod dystrophy caused by mutation in RAB28', 'RAB28 cone-rod dystrophy']",,,,,,,,,,,,
mondo:0100449,FLVCR1-related retinopathy with or without ataxia,"['autosomal recessive posterior column ataxia and retinitis pigmentosa', 'AXPC1', 'posterior column ataxia-retinitis pigmentosa syndrome', 'ataxia, posterior column, with retinitis pigmentosa', 'FLVCR1 retinopathy with or without ataxia', 'PCARP', 'posterior column ataxia with retinitis pigmentosa']",,,,,,,,,,,,
mondo:0100450,CAPN5-related vitreoretinopathy,"['proliferative vitreoretinopathy', 'autosomal dominant neovascular inflammatory vitreoretinopathy', 'retinitis proliferans', 'ADNIV', 'CAPN5 vitreoretinopathy', 'VRNI', 'vitreoretinopathy, neovascular inflammatory', 'vitreoretinopathy, neovascular inflammatory, autosomal dominant']",9719,193235,329211,C4721549,"['-0.2485', '0.001453', '0.2261', '-0.166', '0.1919', '-0.1223', '-0.0288', '0.06012', '0.01823', '-0.02365', '-0.2144', '-0.08417', '-0.1656', '-0.01567', '-0.02365', '-0.04626', '-0.1003', '-0.05438', '0.2242', '-0.559', '0.045', '-0.2107', '0.231', '0.1317', '0.01724', '0.07227', '0.0492', '0.05167', '-0.2515', '0.03564', '0.294', '0.1295', '0.02493', '-0.1547', '0.1081', '0.2119', '-0.0111', '0.2412', '0.114', '-0.5474', '0.1089', '-0.2927', '0.2294', '0.0877', '-0.2202', '-0.2568', '-0.10065', '-0.03812', '0.3274', '-0.0052', '0.0758', '-0.1512', '0.3384', '0.1028', '-0.0673', '-0.44', '0.5405', '0.0992', '-0.692', '-0.0451', '0.2052', '0.02394', '-0.05933', '0.0971', '0.237', '-0.1477', '0.4736', '0.2544', '-0.09454', '0.2954', '-0.1244', '-0.3032', '-0.0668', '0.0839', '-0.007027', '0.01935', '-0.0577', '0.3674', '-0.1622', '-0.2988', '0.02477', '-0.2522', '-0.02669', '0.2269', '-0.564', '-0.2585', '0.1351', '0.3123', '-0.07135', '-0.0967', '0.0671', '0.2429', '-0.0676', '0.0824', '0.5645', '0.125', '0.2178', '-0.2998', '-0.278', '0.08356']",,1001129,D018630,362.29,,10057896,
mondo:0100451,CEP290-related ciliopathy,"['MKS4', 'LCA10', 'JBTS5', 'Senior-Loken syndrome type 6', 'Meckel-Gruber syndrome, type 4', 'amaurosis congenita of Leber, type 10', 'BBS14', 'CEP290 Leber congenital amaurosis', 'Meckel syndrome, type 4', 'Meckel syndrome 4', 'Leber congenital amaurosis 10', 'Meckel-like Cerebrorenodigital syndrome', 'Leber congenital amaurosis caused by mutation in CEP290', 'SENIOR-Loken syndrome 6', 'Joubert syndrome caused by mutation in CEP290', 'Bardet-Biedl syndrome 14', 'Bardet-Biedl syndrome type 14', 'CEP290 ciliopathy', 'Meckel syndrome caused by mutation in CEP290', 'CEP290 Senior-Loken syndrome', 'Joubert syndrome 5', 'CEP290 Joubert syndrome', 'CEP290 Meckel syndrome', 'SLSN6', 'Leber congenital amaurosis type 10', 'Senior-Loken syndrome 6', 'Senior-Loken syndrome caused by mutation in CEP290', 'Joubert syndrome type 5']",,,,,,,,,,,,
mondo:0100452,RPE65-related dominant retinopathy,"['dominant RPE65 retinopathy', 'RP87', 'retinitis pigmentosa 87 with choroidal involvement']",0112144,,,,,,,,,,,
mondo:0100453,GUCY2D-related recessive retinopathy,"['Leber congenital amaurosis caused by mutation in GUCY2D', 'amaurosis congenita of Leber, type 1', 'night blindness, congenital stationary, type 1I', 'CORD6', 'amaurosis congenita of Leber 1', 'cone-rod dystrophy type 6', 'GUCY2D Leber congenital amaurosis', 'CRB', 'GUCY2D cone-rod dystrophy', 'LCA', 'cone-rod dystrophy 6', 'Leber congenital amaurosis 1', 'amaurosis congenita of Leber I', 'LCA1', 'Leber congenital amaurosis type 1', 'retinal cone dystrophy 2', 'RCD2', 'cone-rod dystrophy caused by mutation in GUCY2D', 'recessive GUCY2D retinopathy', 'retinal blindness, congenital']",,,,,,,,,,,,
mondo:0100454,GUCY2D retinopathy,['retinopathy caused by mutation in GUCY2D'],,,,,,,,,,,,
mondo:0100455,neonatal-onset developmental and epileptic encephalopathy,,,,,,,,,,,,,
mondo:0100456,neonatal encephalopathy with non-epileptic myoclonus,,,,,,,,,,,,,
mondo:0100457,"achalasia, familial esophageal","['achalasia, familial esophageal']",,200400,,C1860213,,,,C536011,,,,
mondo:0100458,MECOM-associated syndrome,,,,,,,,,,,,,
mondo:0100459,azoospermia,,14227,,,C0004509,"['-0.0394', '0.02538', '0.002691', '-0.02783', '0.02863', '-0.0717', '0.00794', '0.04944', '-0.02583', '-0.0284', '0.02448', '0.01938', '-0.0253', '0.011345', '-0.00948', '-0.02829', '0.005257', '-0.013885', '-0.01753', '-0.0702', '-0.02228', '-0.01429', '0.0255', '-0.02298', '0.03287', '-0.00786', '-0.00545', '-0.02075', '0.004475', '-0.03023', '0.0556', '-0.01794', '0.05276', '0.010735', '0.02388', '-0.0356', '-0.01146', '-0.014', '0.0126', '-0.0571', '0.03043', '-0.04132', '0.004044', '-0.0283', '-0.01258', '-0.0684', '0.00949', '0.02235', '0.01024', '0.02846', '-0.03372', '0.005005', '-0.03012', '0.03607', '-0.007412', '0.01529', '0.051', '-0.02815', '-0.07007', '0.004986', '0.04202', '0.02985', '-0.001233', '0.0059', '-0.006', '0.01715', '0.01901', '0.0376', '-0.04953', '0.04007', '-0.02681', '0.022', '0.00799', '-0.02591', '-0.010376', '0.012856', '0.00741', '-0.00226', '-0.04486', '0.01282', '0.002718', '0.00629', '0.00089', '0.03412', '0.000682', '0.0004716', '0.00608', '0.03632', '0.05804', '-0.02759', '-0.01184', '0.0462', '-0.02647', '0.03198', '0.08954', '0.02397', '0.03326', '-0.06192', '-0.0259', '0.01281']",,0000279,D053713,606.0,,,
mondo:0100460,"tobacco addiction, susceptibility to","['nicotine dependence, protection against', 'nicotine addiction, protection from', 'smoking habit, susceptibility to', 'nicotine dependence, susceptibility to', 'nicotine addiction, susceptibility to', 'cigarette habituation, susceptibility to', 'susceptibility to tobacco addiction', 'tobacco addiction, susceptibility to']",,188890,,,,,,,,,,
mondo:0100462,"short stature and advanced bone age, with or without early-onset osteoarthritis and/or osteochondritis dissecans","['OD', 'osteochondritis dissecans, short stature, and early-onset osteoarthritis', 'SSOAOD', 'osteochondritis dissecans and short stature']",,165800,251262,,,,,,,,,
mondo:0100463,"methylmalonic aciduria and/or homocystinuria, cblD type",,,,,,,,,,,,,
mondo:0100464,acid sphingomyelinase deficiency,,,,,,,,,,,,,
mondo:0100465,complex neurodevelopmental disorder with or without congenital anomalies,,,,,,,,,,,,,
mondo:0100466,butterfly-shaped pigment dystrophy,"['butterfly-shaped pattern dystrophy', 'butterfly-shaped pigment dystrophy', 'butterfly-shaped pigmentary macular dystrophy']",,,99001,C4511237,,,,,,,,
mondo:0100467,preeclampsia/eclampsia 1,"['hemolysis, elevated liver enzymes, and low platelet count', 'hypertension, pregnancy-induced', 'PREG1', 'PEE1', 'toxemia of pregnancy', 'toxaemia of pregnancy', 'PREECLAMPSIA/eclampsia 1']",,189800,,,,,,,,,,
mondo:0100468,Batten-Turner congenital myopathy,,0081335,255300,,,,,,,,,,
mondo:0100469,"anosmia, isolated congenital, X-linked",,,301700,,,,,,,,,,
mondo:0100470,reactive airway disease,"['reactive airway disease (AQ)', 'hyperactive airway disease']",,,,,,C113673,,,,,,
mondo:0100471,vitamin D deficiency,"['DEFIC VITAMIN D', 'vitamin D deficiency (disorder)', 'deficiencies, vitamin D', 'VITAMIN D DEFIC', 'vitamin D deficiency, NOS', 'deficiency, vitamin D', 'avitaminosis D, NOS', 'deficiency of vitamin D (disorder)', 'vitamin D deficiencies', 'vitamin D insufficiency', 'avitaminosis D']",10574,,,C0042870,,C114830,0003762,D014808,268,E55,,0100512
mondo:0100472,lissencephaly spectrum disorder with complex brainstem malformation,,,,,,,,,,,,,
mondo:0100473,disorder of peptide and amine metabolism,,,,,,,,,,,,,
mondo:0100474,mild ichthyosis vulgaris,,,,,,,,,,,,,
mondo:0100475,severe ichthyosis vulgaris,,,,,,,,,,,,,
mondo:0100476,"lipodystrophy, partial, acquired, susceptibility to","['lipodystrophy, cephalothoracic type', 'lipodystrophy, partial, acquired, susceptibility', 'lipodystrophy, partial, progressive', 'barraquer-simons syndrome', 'APLD, susceptibility to']",,608709,,C3887501,,,,,,,,
mondo:0100477,disorder of methylamine metabolism,,,,,,,,,,,,,
mondo:0100478,brain malformations with or without urinary tract defects,,,613735,,,,,,,,,,
mondo:0100479,rifampicin-resistant tuberculosis,"['RR-TB', 'rifampicin-resistant TB']",,,,,,,,,,,,
mondo:0100480,autoimmune primary adrenal insufficiency,"['autoimmune adrenalitis', 'autoimmune Addison^s disease']",,,85138,,,C113814,,,,,,
mondo:0100481,active tuberculosis,['active TB'],,,,,,,,,,,,
mondo:0100482,extensively drug-resistant tuberculosis,['XDR-TB'],,,,,,C128417,,D054908,,,,
mondo:0100483,totally drug-resistant tuberculosis,['TDR-TB'],,,,,,,,,,,,
mondo:0100484,TSPAN12-related vitreoretinopathy,"['TSPAN12 exudative vitreoretinopathy', 'exudative vitreoretinopathy 5', 'exudative vitreoretinopathy caused by mutation in TSPAN12']",,,,,,,,,,,,
mondo:0100485,KCNH1 associated disorder,,,,,,,,,,,,,
mondo:0100486,adult acne,"['acne, adult']",,604324,,,,,,C565791,,,,
mondo:0100487,TPM4-related platelet disorder,,,,,,,,,,,,,
mondo:0100488,CDH1-related diffuse gastric and lobular breast cancer syndrome,"['LBC', 'gastric cancer, hereditary diffuse', 'DGLBC', 'HDGC', 'gastric cancer, familial diffuse breast cancer, lobular', 'diffuse gastric and lobular breast cancer syndrome']",,137215,,,,,,,,,,
mondo:0100489,"Graves disease, susceptibility to, 1","['Graves disease, susceptibility to, 1']",,275000,,,,,,,,,,
mondo:0100490,"breasts and/or nipples, aplasia or hypoplasia of, 1","['amazia', 'breasts and/or nipples, aplasia or hypoplasia of, 1', 'amastia', 'BNAH1', 'athelia']",,113700,,,,,,,,,,
mondo:0100491,generalized pustular psoriasis,,,,,C0343055,,,,,,L40.1,,
mondo:0100492,Bonnevie-Ullrich syndrome,"['Bonnevie-Ullrich syndrome', 'Bonnevie-Ulrich syndrome']",3491,,,,,C34434,,,,,,
mondo:0100493,autosomal recessive titinopathy,"['TTN-related myopathy, autosomal recessive']",,,,,,,,,,,,
mondo:0100494,autosomal dominant titinopathy,"['TTN-related myopathy, autosomal dominant']",,,,,,,,,,,,
mondo:0100495,autosomal recessive distal titinopathy,['distal titinopathy'],,,,,,,,,,,,
mondo:0100496,Emery-Dreifuss-like muscular dystrophy,,,,,,,,,,,,,
mondo:0100497,titinopathy with congenital contractures,,,,,,,,,,,,,
mondo:0100498,UROD-related inherited porphyria,,,,,,,,,,,,,
mondo:0100499,multiple congenital anomalies due to 14q32.2 imprinting defect,,,,,,,,,,,,,
mondo:0100500,Mendelian neurodevelopmental disorder,,,,,,,,,,,,,
mondo:0100501,body-stalk anomaly,"['body stalk anomaly', 'LBWC', 'body stalk complex', 'BSA', 'limb body wall complex']",,,2369,,,,,,,,,
mondo:0100502,NTHL1-deficiency tumor predisposition syndrome,,,,,,,,,,,,,
mondo:0100503,DPH5-related diphthamide-deficiency syndrome,,,,,,,,,,,,,
mondo:0100504,fungal infection of the toenail,,,,,,,,,,,,,
mondo:0100505,food dermatitis,['dermatitis due to food taken internally'],,,,,,C34534,,,,,,
mondo:0100506,Cockayne spectrum with or without cerebrooculofacioskeletal syndrome,,,,,,,,,,,,,
mondo:0100507,multiple congenital anomalies due to 14q32.2 paternally expressed gene defect,['Temple syndrome'],,,,,,,,,,,,
mondo:0100508,salivary gland type cancer of the breast,['salivary gland type carcinoma of the breast'],,,213557,,,,,,,C50.6,,
mondo:0100509,IFT140-related recessive ciliopathy,"['short-rib thoracic dysplasia 9 with or without polydactyly', 'IFT140-related recessive ciliopathy', 'retinitis pigmentosa 80']",,,,,,,,,,,,
mondo:0100510,spondyloepimetaphyseal dysplasia,"['spondylo-epi-(meta)-physeal dysplasia', 'SEMD']",0080027,,,,,,,,,,,
mondo:0100511,sudden cardiac arrest,,,,,,"['0.1665', '0.4023', '-0.8384', '0.1118', '-0.2231', '-0.756', '0.4512', '0.8516', '0.1189', '-0.5024', '0.4458', '-0.00817', '0.2244', '0.329', '-0.4978', '-0.2408', '-0.4316', '-0.416', '-0.9146', '-0.6763', '0.4858', '0.4543', '-0.047', '0.09735', '0.2722', '-1.36', '-0.014', '0.3713', '0.3623', '0.2262', '0.543', '0.1738', '0.2712', '0.0829', '0.1621', '0.07745', '0.4277', '0.3203', '0.5347', '-0.2554', '0.406', '-0.2163', '0.2057', '-0.1189', '0.2656', '0.04468', '-0.5283', '0.05746', '0.384', '-0.10583', '0.03427', '0.2184', '-0.087', '-0.2009', '-0.1035', '-0.1818', '-0.7324', '0.5513', '-0.3176', '-0.1488', '-0.484', '0.6475', '-0.1934', '-0.2695', '-0.6426', '-0.4324', '0.6235', '0.6', '-0.66', '0.1682', '-0.5005', '0.778', '-0.0689', '-0.2864', '0.632', '0.31', '0.05902', '0.2507', '-0.3909', '-0.11414', '-0.1486', '0.0163', '-0.4998', '-0.1383', '0.2676', '-0.0644', '0.589', '0.354', '0.3079', '0.11633', '-0.1354', '-0.647', '-0.1368', '0.7295', '0.1808', '0.1392', '-0.0368', '-0.6035', '-0.9805', '0.6294']",,0004278,C1720824,,,,
mondo:0100512,"mitochondrial DNA depletion syndrome, hepatocerebral form","['deoxyguanosine kinase deficiency', 'mtDNA depletion syndrome, hepatocerebral form']",,,254871,CN069134,"['-0.1903', '0.1611', '0.0876', '0.0587', '0.05984', '-0.1611', '-0.01401', '0.1348', '-0.1245', '-0.06586', '-0.001582', '-0.05615', '0.03622', '-0.01008', '-0.033', '-0.1339', '-0.0803', '-0.06714', '-0.08826', '-0.2339', '-0.005257', '-0.10254', '0.1118', '-0.02397', '0.0753', '0.02151', '-0.0956', '-0.02287', '0.02457', '-0.063', '0.05038', '0.1176', '0.2144', '0.03038', '-0.02164', '-0.1009', '-0.06152', '-0.0943', '-0.0393', '-0.1534', '0.06964', '-0.2063', '-0.01166', '-0.003384', '-0.0607', '-0.1131', '-0.06198', '0.03107', '0.1295', '0.008385', '-0.08246', '-0.0778', '0.02611', '0.01521', '-0.0644', '-0.0934', '0.1726', '-0.02507', '-0.1282', '0.08685', '0.1425', '-0.02007', '0.0934', '0.01187', '-0.02686', '-0.008965', '0.1255', '0.06726', '-0.1713', '0.2133', '-0.148', '0.00784', '0.05865', '0.0327', '0.03256', '0.11566', '-0.00545', '0.03372', '-0.1456', '-0.00918', '0.04184', '0.05154', '-0.091', '0.104', '-0.03152', '0.02655', '0.11835', '0.1543', '0.1637', '0.0841', '0.1407', '0.0964', '-0.02428', '-0.03128', '0.1953', '0.1976', '0.1572', '-0.2188', '-0.02443', '0.0702']",,,C580039,,,,
mondo:0100513,TRAF3 haploinsufficiency,,,,,,,,,,,,,
mondo:0100514,familial ovarian carcinoma,"['hereditary ovarian carcinoma', 'familiar ovarian carcinoma', 'familial ovarian carcinoma', 'hereditary ovarian cancer']",6901,,,C1333992,,C36102,,,,,,
mondo:0100515,mirror movements 1 and/or agenesis of the corpus callosum,,,,,,,,,,,,,
mondo:0100516,complex neurodevelopmental disorder with motor features,,,,,,,,,,,,,
mondo:0100517,PSAP-related sphingolipidosis,,,,,,,,,,,,,
mondo:0100518,hereditary attention deficit-hyperactivity disorder,,,143465,,,,,,,,,,
mondo:0100519,"epilepsy, idiopathic generalized, susceptibility to, 17",['EIG17'],,602477,,C5561931,,,,,,,,
mondo:0100520,NKX2-1 related choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction,,,,,,,,,,,,,
mondo:0100521,NOG-related symphalangism spectrum disorder,['NOG-SSD'],,,,,,,,,,,,
mondo:0100522,hypotrichosis 4,"['hypotrichosis type 4', 'hypotrichosis, Marie Unna type, 1', 'Marie Unna hereditary hypotrichosis 1', 'hypotrichosis 4', 'MUHH1', 'HYPT4']",0110701,146550,,C2750815,,,,C567718,,,,
mondo:0100523,SPAST-related motor disorder,,,,,,,,,,,,,
mondo:0100524,ASAH1-related sphingolipidosis,['acid ceramidase deficiency'],,,,,,,,,,,,
mondo:0100525,TCF7L2-related neurodevelopmental disorder,,,,,,,,,,,,,
mondo:0100526,"breast-ovarian cancer, familial, susceptibility to",,,,,,,,,,,,,
mondo:0100527,"dysplastic cortical hyperostosis, Kozlowski-Tsuruta type",['Kozlowski-Tsuruta syndrome'],,,2204,,,,,,,,,
mondo:0100528,Hao-Fountain syndrome due to 16p13.2 microdeletion,"['16p13.2 microdeletion syndrome', 'chromosome 16P13.2 deletion syndrome', 'Del(16)(p13.2)', 'monosomy 16p13.2', 'chromosome 16p13.2 deletion syndrome']",,,500055,,,,,,,,,
mondo:0200000,uterine ligament adenosarcoma,['uterine ligament adenosarcoma'],,,,C3640823,,C102570,,,,,,
mondo:0300000,SSR3-CDG,,,,,,,,,,,,,
mondo:0400000,small intestinal bacterial overgrowth,['SIBO'],,,,,,,,,,,,
mondo:0400002,calcium-alkali syndrome,,,,,,,,,,,,,
mondo:0400003,skeletal fluorosis,,,,,,,,,,,,,
mondo:0400004,phrynoderma,,,,,,,,,,,,,
mondo:0400005,refeeding syndrome,,,,,,,,,D055677,,,,
mondo:0400006,botryomycosis,"['pyoderma vegetans', 'bacterial pseudomycosis']",,,,,,,,,,,,
mondo:0500000,episodic angioedema with eosinophilia,"['EAE', 'Gleich^s syndrome', 'Gleich syndrome']",,,,,,,,,,,,
mondo:0500018,acute fibrinous and organizing pneumonia,['AFOP'],,,,,,,,,,,,
mondo:0550003,SEC61B-related polycystic liver disease,,,,,,,,,,,,,
mondo:0600001,glutaminase deficiency,,,,,,,,,,,,,
mondo:0600002,hemorrhagic fever,['haemorrhagic fever'],,,,,,C36169,,,,,,
mondo:0600003,bacterial hemorrhagic fever,"['haemorrhagic fever, bacterial', 'bacterial haemorrhagic fever']",,,,,,,,,,,,
mondo:0600005,venom allergy,"['venom hypersensitivity', 'IgE-mediated venom hypersensitivity']",,,,,,,,,,,,
mondo:0600008,cytokine release syndrome,"['cytokine-associated toxicity', 'CRS', 'cytokine storm']",,,,,,C78251,,D000080424,,,,
mondo:0600009,severe hypophosphatasia,,,,,,,,,,,,,
mondo:0600010,moderate hypophosphatasia,,,,,,,,,,,,,
mondo:0600011,mild hypophosphatasia,['attenuated hypophosphatasia'],,,,,,,,,,,,
mondo:0600014,alveolar capillary dysplasia without misalignment of pulmonary veins,['ACD without misalignment'],,,,,,,,,,,,
mondo:0600016,acinar dysplasia,['AcDys'],,,,,,,,,,,,
mondo:0600017,acinar dysplasia caused by mutation in FGF10,"['FGF10 acinar dysplasia', 'FGF10 related acinar dysplasia']",,,,,,,,,,,,
mondo:0600018,acinar dysplasia caused by mutation in FGFR2,"['FGFR2 acinar dysplasia', 'FGFR2 related acinar dysplasia']",,,,,,,,,,,,
mondo:0600019,acinar dysplasia caused by mutation in TBX4,"['TBX4 related acinar dysplasia', 'TBX4 acinar dysplasia']",,,,,,,,,,,,
mondo:0600023,idiopathic inflammatory myopathy,['idiopathic myositis'],,,,C0751356,,C116796,,,,,,
mondo:0600024,familial idiopathic inflammatory myopathy,['familial idiopathic myositis'],,160750,,,,,,C000598744,,,,
mondo:0600025,hydrosalpinx,"['fallopian tube obstruction', 'blocked fallopian tube']",,,,,,C142886,,,,,,
mondo:0600026,vanishing lung syndrome,"['VLS', 'idiopathic giant bullous emphysema']",,,,,,,,,,,,
mondo:0600027,congenital right-sided heart lesions,,,,,,,,0600032,,,,,
mondo:0600029,restrictive pulmonary disease,"['restrictive lung disease', 'Restrictive lung disease (disorder)']",,,,C0085581,,C91762,,,,,,
mondo:0600030,B-cell acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1),"['B acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)', 'B-lymphoblastic leukemia/lymphoma with TCF3-PBX1', 'B acute lymphoblastic leukaemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)', 'B lymphoblastic leukemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) (morphologic abnormality)', 'B-acute lymphoblastic leukemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)', 'B lymphoblastic leukaemia lymphoma with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1) (morphologic abnormality)', 'B-acute lymphoblastic leukaemia with t(1;19)(q23;p13.3); E2A-PBX1 (TCF3-PBX1)', 'B-lymphoblastic leukemia/lymphoma with t(1;19)(q23;p13.3)']",0080649,,585956,,,C80347,,,,,,
mondo:0700000,ALG9-associated autosomal dominant polycystic kidney disease,"['ALG9-associated ADPKD', 'ALG9 related autosomal dominant polycystic kidney disease', 'ALG9 autosomal dominant polycystic kidney disease', 'autosomal dominant polycystic kidney disease caused by mutation in ALG9']",,,,,,,,,,,,
mondo:0700001,shrinking lung syndrome,"['shrinking of the lung', 'small lungs', 'SLS']",,,,,,,,,,,,
mondo:0700002,ATP1A3-associated neurological disorder,"['ATP1A3 neurological disorder', 'neurological disorder caused by mutation in ATP1A3', 'ATP1A3 related neurological disorder']",,,,,,,,,,,,
mondo:0700003,obstetric disorder,,,,,,,,,,,,,
mondo:0700004,idiopathic vs non-idiopathic,,,,,,,,,,,,,
mondo:0700005,idiopathic,,,,,,,,,,,,,
mondo:0700006,non-idiopathic,,,,,,,,,,,,,
mondo:0700007,idiopathic disease,['idiopathic disorder'],,,,,,,,,,,,
mondo:0700008,chromosome 1 disorder,,,,,,,,,,,,,
mondo:0700009,chromosome 2 disorder,,,,,,,,,,,,,
mondo:0700010,chromosome 3 disorder,,,,,,,,,,,,,
mondo:0700011,chromosome 4 disorder,,,,,,,,,,,,,
mondo:0700012,chromosome 5 disorder,,,,,,,,,,,,,
mondo:0700013,chromosome 6 disorder,,,,,,,,,,,,,
mondo:0700014,chromosome 7 disorder,,,,,,,,,,,,,
mondo:0700015,chromosome 8 disorder,['anomaly of chromosome pair 8'],,,,C0265418,,,,,,,,
mondo:0700016,chromosome 9 disorder,,,,,,,,,,,,,
mondo:0700017,chromosome 10 disorder,,,,,,,,,,,,,
mondo:0700018,chromosome 11 disorder,,,,,,,,,,,,,
mondo:0700019,chromosome 12 disorder,,,,,,,,,,,,,
mondo:0700020,chromosome 13 disorder,,,,,,,,,,,,,
mondo:0700021,chromosome 14 disorder,,,,,,,,,,,,,
mondo:0700022,chromosome 15 disorder,,,,,,,,,,,,,
mondo:0700023,chromosome 16 disorder,,,,,,,,,,,,,
mondo:0700024,chromosome 19 disorder,,,,,,,,,,,,,
mondo:0700025,chromosome 20 disorder,,,,,,,,,,,,,
mondo:0700026,chromosome 22 disorder,,,,,,,,,,,,,
mondo:0700027,chromosome X disorder,,,,,,,,,,,,,
mondo:0700028,chromosome Y disorder,,,,,,,,,,,,,
mondo:0700029,partial duplication of chromosome 13,,,,,,,,,,,,,
mondo:0700030,complete trisomy 21,['standard trisomy 21'],,,,,,,,,,,,
mondo:0700031,mosaic trisomy 18,,,,,,,,,,,,,
mondo:0700032,complete trisomy 18,,,,,,,,,,,,,
mondo:0700033,complete trisomy 13,,,,,,,,,,,,,
mondo:0700034,mosaic trisomy 13,['trisomy 13 mosaicism'],,,,,,,,,,,,
mondo:0700035,monosomy chromosome 8,"['chromosome 8 deletion', 'loss of chromosome 8']",,,,,,C36535,,C537823,,,,
mondo:0700036,fibrothecoma,,,,,,,,,,,,,
mondo:0700037,testicular fibrothecoma,,,,,,,,,,,,,
mondo:0700038,TDP-43 proteinopathy,,,,,C2718017,,,,D057177,,,,
mondo:0700039,bladder exstrophy-epispadias-cloacal extrophy complex,['BEEC'],,600057,,C1838703,,,,,,,,
mondo:0700040,neonatal jaundice due to ABO incompatibility,,,,,,,,,,,,,
mondo:0700041,"neuroblastoma, susceptibility to, 2","['NBLST2', 'neuroblastoma, susceptibility to, type 2', 'susceptibility to neuroblastoma 2']",,613013,,,,,,,,,,
mondo:0700042,X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency,"['X-linked MSMD due to NEMO deficiency', 'X-linked mendelian susceptibility to mycobacterial diseases due to NEMO deficiency', 'X-linked mendelian susceptibility to mycobacterial diseases caused by mutation in IKBKG', 'X-linked MSMD due to IKBKG deficiency', 'IKBKG X-linked mendelian susceptibility to mycobacterial diseases', 'X-linked mendelian susceptibility to mycobacterial diseases due to IKBKG deficiency']",,,319612,C1845073,"['-0.2354', '0.2477', '0.0317', '-0.075', '0.1733', '-0.3293', '0.03238', '-0.0511', '-0.1241', '-0.261', '0.07935', '0.0987', '-0.2012', '0.03882', '0.2947', '-0.1492', '-0.04233', '0.04285', '-0.2161', '-0.3188', '0.1056', '-0.1203', '0.1672', '-0.00811', '-0.136', '-0.03214', '-0.11224', '0.02325', '-0.10425', '-0.2039', '0.10046', '0.1152', '0.3271', '0.0942', '0.179', '-0.287', '0.002281', '-0.1888', '-0.0941', '-0.2457', '0.001715', '-0.1265', '0.1464', '-0.09186', '-0.2496', '-0.3904', '0.0847', '-0.02417', '0.1362', '0.0898', '-0.0685', '-0.2156', '0.2451', '0.0381', '-0.09247', '-0.103', '0.4036', '-0.0276', '-0.1759', '0.1921', '0.06088', '0.2274', '0.1648', '0.12006', '0.2664', '0.2012', '0.1367', '0.1181', '-0.2559', '0.2323', '-0.2223', '-0.10077', '0.004498', '-0.1593', '0.1871', '0.1084', '0.1244', '0.0794', '-0.0098', '0.1677', '-0.1448', '0.03183', '0.05365', '0.1776', '-0.056', '-0.1625', '0.3845', '0.3164', '0.3232', '0.04047', '0.1793', '0.11', '-0.0976', '-0.2017', '0.6035', '0.454', '0.265', '-0.3406', '-0.03032', '-0.0276']",,,C564468,,,,
mondo:0700043,syndrome caused by partial chromosomal duplication of the short arm of chromosome 9,,,,,,,,,,,,,
mondo:0700044,TUBB2A-related tubulinopathy,,,,,,,,,,,,,
mondo:0700045,protothecosis,,,,,,,,,,,,,
mondo:0700046,baclofen withdrawal syndrome,,,,,,,,,,,,,
mondo:0700047,premenopausal osteoporosis,,,,,,,,,,,,,
mondo:0700048,hand-foot syndrome,['palmar-plantar erythrodysthesia'],,,,C0549410,,C27177,,D060831,,,,
mondo:0700049,"infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700050,"bacterial infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700051,liver abscess (disease),"['abscess of liver', 'hepatic abscess']",,,,,,C99089,,,,,,
mondo:0700052,intersphincteric abscess,,,,,,,,,,,,,
mondo:0700053,"viral infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700054,microcephaly 6 with or without short stature,,,,,,,,,,,,,
mondo:0700055,KIF1A related neurological disorder,"['KIF1A neurological disorder', 'KAND', 'neurological disorder caused by mutation in KIF1A', 'neurological disorder caused by variation in KIF1A']",,,,,,,,,,,,
mondo:0700056,"fungal infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700057,neurological pain disorder,"['neurological pain disease', 'neurologic pain syndrome']",,,,,,,,,,,,
mondo:0700058,Morton neuroma,"['interdigital neuralgia', 'interdigital nerve compression syndrome', 'Morton metatarsalgia', 'interdigital neuritis', 'interdigital neuroma', 'intermetatarsal neuroma', 'Morton entrapment']",,,,,,C4075,,,,,,
mondo:0700059,"Actinobacillus infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700060,"leukemia, acute, X-linked",,,308960,,,,,,,,,,
mondo:0700061,mosaic vs complete,,,,,,,,,,,,,
mondo:0700062,mosaic,,,,,,,,,,,,,
mondo:0700063,complete,,,,,,,,,,,,,
mondo:0700064,aneuploidy,['chromosome number anomaly'],,,,,,C2873,,D000782,,,,
mondo:0700065,trisomy,['chromosomal triplication'],,,,,,C3421,,D014314,,,,
mondo:0700066,myopathy caused by variation in FKRP,"['FKRP myopathy', 'FKRP-related myopathy', 'myopathy caused by mutation in FKRP']",,,,,,,,,,,,
mondo:0700067,myopathy caused by variation in FKTN,"['FKTN-related myopathy', 'myopathy caused by mutation in FKTN', 'FKTN myopathy']",,,,,,,,,,,,
mondo:0700068,myopathy caused by variation in POMGNT1,"['POMGNT1-related myopathy', 'POMGNT1 myopathy', 'myopathy caused by mutation in POMGNT1']",,,,,,,,,,,,
mondo:0700069,myopathy caused by variation in POMGNT2,"['POMGNT2 myopathy', 'myopathy caused by mutation in POMGNT2', 'POMGNT2-related myopathy']",,,,,,,,,,,,
mondo:0700070,myopathy caused by variation in POMT1,"['myopathy caused by mutation in POMT1', 'POMT1-related myopathy', 'POMT1 myopathy']",,,,,,,,,,,,
mondo:0700071,myopathy caused by variation in POMT2,"['POMT2-related myopathy', 'myopathy caused by mutation in POMT2', 'POMT2 myopathy']",,,,,,,,,,,,
mondo:0700072,"Rhabdoviridae infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700073,glutaric acidemia IIa,"['multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFA', 'GA2A', 'glutaric acidemia 2A', 'ETFA deficiency']",,,,,,,,,,,,
mondo:0700074,glutaric acidemia IIb,"['GA2B', 'ETFB deficiency', 'multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFB', 'glutaric acidemia 2B']",,,,,,,,,,,,
mondo:0700075,congenital muscular dystrophy caused by variation in POMGNT2,"['congenital muscular dystrophy-POMGNT2 related', 'congenital muscular dystrophy caused by mutation in POMGNT2']",,,,,,,,,,,,
mondo:0700076,glutaric acidemia IIc,"['glutaric acidemia 2C', 'multiple acyl-CoA dehydrogenase deficiency caused by mutation in ETFDH', 'ETFDH deficiency', 'GA2C']",,,,,,,,,,,,
mondo:0700077,vitiligo-associated multiple autoimmune disease susceptibility 6,['VAMAS6'],,193200,,,,,,,,,,
mondo:0700078,triple-positive breast carcinoma,"['triple positive breast cancer', 'HR-positive HER2 positive breast cancer', 'hormone receptor positive her2 positive breast cancer']",,,,C5243562,,C118311,,,,,,
mondo:0700079,hormone receptor-positive breast cancer,,,,,C5442556,,C157056,,,,,,
mondo:0700080,EPHB4-associated vascular malformation spectrum,,,,,,,,,,,,,
mondo:0700081,newborn respiratory distress syndrome,"['hyaline membrane disease', 'neonatal respiratory distress', 'respiratory distress syndrome of newborn', 'respiratory distress syndrome Of newborns', 'HMD - hyaline membrane disease', 'neonatal respiratory distress syndrome', 'infant ARDS', 'syndrome Of newborns (RDS), respiratory distress', 'RDS, respiratory distress syndrome Of newborns', 'RDS of prematurity', 'RDS Of newborns', 'respiratory distress syndrome in the newborn', 'RDS', 'RDS - infants', 'respiratory distress syndrome, infant', 'pulmonary hypoperfusion syndrome of newborn', 'respiratory distress syndrome', 'respiratory distress syndrome Of newborns (RDS)', 'infant acute respiratory distress syndrome', 'infant respiratory distress syndrome', 'respiratory distress syndrome in premature infants', 'pulmonary hyaline membrane disease', 'newborns (RDS), respiratory distress syndrome Of', 'NRDS']",12716,,,C0035220,,C27560,,,769,,,
mondo:0700082,Robertsonian translocation Down syndrome,,,,,,,C188150,,,,,,
mondo:0700083,reciprocal translocation down syndrome,,,,,,,,,,,,,
mondo:0700084,myopathy caused by variation in GMPPB,"['GMPPB-related myopathy', 'myopathy caused by mutation in GMPPB']",,,,,,,,,,,,
mondo:0700085,pentasomy,,,,,,,,,,,,,
mondo:0700086,uniparental disomy,,,,,,,C85215,,D024182,,,,
mondo:0700087,Usher syndrome type 1B,"['Usher syndrome, type 1B']",,276900,,,,,,C536485,,,,
mondo:0700088,paroxysmal nonkinesigenic dyskinesia,"['paroxysmal non-kinesigenic dyskinesia', 'Paroxysomal nonkinesigenic dyskinesia', 'DYT-MR-1', 'Paroxystic non-kinesigenic choreoathetosis']",,,98810,,"['-0.01467', '0.1262', '-0.003521', '-0.065', '-0.002846', '-0.1149', '0.08026', '0.05966', '-0.05817', '-0.02896', '-0.01035', '-0.01265', '-0.01352', '-0.005733', '-0.004433', '-0.01158', '-0.0011015', '-0.1099', '-0.001578', '-0.1362', '-0.001795', '0.004623', '0.0153', '-0.04678', '0.004387', '0.006924', '-0.02202', '-0.0503', '-0.01344', '-0.03015', '0.02954', '0.02942', '0.09735', '0.03223', '-0.010994', '-0.007454', '-0.01547', '-0.03964', '-0.0494', '-0.03616', '0.06494', '-0.1225', '0.001823', '0.001678', '0.04486', '-0.03006', '-0.04437', '0.0982', '0.02666', '0.0887', '-0.05368', '0.04248', '0.02513', '-0.00918', '0.01646', '0.00357', '0.1394', '-0.0648', '-0.05154', '-0.01216', '0.02216', '0.05734', '0.04883', '0.011055', '-0.04108', '-0.01245', '0.08966', '0.0675', '-0.0852', '0.08685', '-0.05527', '0.02205', '0.01159', '-0.07666', '0.006924', '0.05902', '0.06168', '-0.005455', '-0.05164', '-0.04343', '0.006275', '0.02072', '-0.014854', '0.0874', '0.02477', '0.00965', '0.04153', '0.04868', '0.0943', '0.03625', '0.0355', '0.03506', '0.02618', '0.0521', '0.151', '0.0573', '0.085', '-0.05817', '-0.05566', '0.03156']",,,,,,,
mondo:0700089,paroxysmal nonkinesigenic dyskinesia 1,"['PNKD1', 'paroxysmal dystonic choreoathetosis', 'PNKD paroxysmal dyskinesia', 'paroxysmal dyskinesia caused by mutation in PNKD', 'paroxysmal nonkinesigenic dyskinesia type 1', 'PxMD-PNKD', 'choreoathetosis, familial paroxysmal', 'choreoathetosis, nonkinesigenic', 'mount-reback syndrome', 'dystonia 8', 'paroxysmal nonkinesigenic dyskinesia 1']",0090049,118800,,,,,,,,,10065658,
mondo:0700090,"epilepsy, familial temporal lobe, 1","['ETL1', 'epilepsy, lateral temporal lobe, autosomal dominant', 'epilepsy, partial, with auditory features', 'epilepsy, familial temporal lobe, type 1']",,600512,,,,C141441,,,,,,
mondo:0700091,ring chromosome disorder,['supernumerary circular chromosome'],,,,C0035639,,C3360,,D012303,,,,
mondo:0700092,neurodevelopmental disorder,,,,,C1535926,,C89338,,D065886,,,C1535926,
mondo:0700093,balanced Robertsonian translocation Down syndrome,,,,,,,,,,,,,
mondo:0700094,unbalanced Robertsonian translocation Down syndrome,,,,,,,,,,,,,
mondo:0700095,"Reoviridae infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700096,human disease,['human disease or disorder'],,,,,,,,,,,,
mondo:0700098,"neoplasm, non-human animal",,,,,,,,,,,,,
mondo:0700099,"adenocarcinoma, non-human animal",,,,,,,,,,,,,
mondo:0700100,"leukemia, non-human animal",,,,,,,,,,,,,
mondo:0700101,"carcinoma, non-human animal",,,,,,,,,,,,,
mondo:0700102,"lymphoma, non-human animal",,,,,,,,,,,,,
mondo:0700103,"nutritional deficiency disease, non-human animal",,,,,,,,,,,,,
mondo:0700104,"respiratory system disorder, non-human animal",,,,,,,,,,,,,
mondo:0700105,"difference of sexual differentiation, non-human animal",,,,,,,,,,,,,
mondo:0700106,"immune system disorder, non-human animal",,,,,,,,,,,,,
mondo:0700107,"chromosome 19q13.11 deletion syndrome, distal",,,613026,,,,,,,,,,
mondo:0700108,"prion disease, non-human animal",,,,,,,,,,,,,
mondo:0700109,"skin disease caused by bacterial infection, non-human animal",,,,,,,,,,,,,
mondo:0700110,"pneumonia, non-human animal",,,,,,,,,,,,,
mondo:0700111,"bacterial pneumonia, non-human animal",,,,,,,,,,,,,
mondo:0700112,"heterotaxy, visceral, 5, autosomal","['SIV', 'HTX5', 'situs inversus viscerum', 'NODAL visceral heterotaxy', 'visceral heterotaxy caused by mutation in NODAL']",,270100,,,,,,,,,,
mondo:0700113,"Anaplasmataceae infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700114,"vector-borne disease, non-human animal",,,,,,,,,,,,,
mondo:0700115,proliferative vitreoretinopathy,,,,,C0242852,,,1001129,D018630,,,,
mondo:0700116,microcephaly with lissencephaly and/or hydranencephaly,,,,,,,,,,,,,
mondo:0700117,SLC6A3-related dopamine transporter deficiency syndrome,"['DTDS', 'Dopamine transporter deficiency syndrome']",,,,,,,,,,,,
mondo:0700118,proximal chromosome 18q deletion syndrome,"['proximal 18q deletion', 'proximal 18q deletion syndrome', 'proximal 18q-']",,,,,,,,,,,,
mondo:0700119,distal chromosome 18q deletion syndrome,"['distal 18q deletion syndrome', 'distal 18q-', 'distal 18q deletion']",,,,,,,,,,,,
mondo:0700120,BAFopathy,,,,,,,,,,,,,
mondo:0700121,ACTL6A-related BAFopathy,,,,,,,,,,,,,
mondo:0700122,PBRM1-related BAFopathy,,,,,,,,,,,,,
mondo:0700123,SMARCC1-associated developmental dysgenesis syndrome,['SMARCC1-related BAFopathy'],,,,,,,,,,,,
mondo:0700124,chromosome 21 disorder,,,,,,,,,,,,,
mondo:0700125,chromosome 18 disorder,,,,,,,,,,,,,
mondo:0700126,trisomy 21,,,,,,,,,,,,,
mondo:0700127,mosaic trisomy 21,,,,,,,,,,,,,
mondo:0700128,translocation Down syndrome,['Robertsonian Translocation Trisomy 21'],,,,,,,,,,,,
mondo:0700129,mosaic translocation Down syndrome,,,,,,,,,,,,,
mondo:0700130,partial segmental duplication,"['segmental duplication', 'partial trisomy 21']",,,,,,,,,,,,
mondo:0700131,"sarcoma, non-human animal",,,,,,,,,,,,,
mondo:0700132,"melanoma, non-human animal",,,,,,,,,,,,,
mondo:0700133,"adenoma, non-human",,,,,,,,,,,,,
mondo:0700134,bovine neoplasm,,,,,,,C134527,,,,,,
mondo:0700135,bovine leukemia,,,,,,,C131469,,,,,,
mondo:0700136,bovine protoporphyria,,,,,,,C131472,,,,,,
mondo:0700137,bovine lymphosarcoma,,,,,,,C134767,,,,,,
mondo:0700138,bovine rectal myxoma,,,,,,,C134768,,,,,,
mondo:0700139,canine neoplasm,,,,,,,C134526,,,,,,
mondo:0700140,canine osteosarcoma,,,,,,,C120045,,,,,,
mondo:0700141,canine melanoma,,,,,,,C120298,,,,,,
mondo:0700142,canine hemangiosarcoma,,,,,,,C122783,,,,,,
mondo:0700143,canine mammary carcinoma,,,,,,,C124249,,,,,,
mondo:0700144,canine leukemia,,,,,,,C128120,,,,,,
mondo:0700145,canine lymphoma,,,,,,,C128121,,,,,,
mondo:0700146,canine prostate carcinoma,,,,,,,C128122,,,,,,
mondo:0700147,canine histiocytic sarcoma,,,,,,,C128125,,,,,,
mondo:0700148,canine transitional cell carcinoma,,,,,,,C128126,,,,,,
mondo:0700149,canine sarcoma,,,,,,,C128195,,,,,,
mondo:0700150,canine mastocytoma,,,,,,,C129077,,,,,,
mondo:0700151,canine glioma,,,,,,,C129297,,,,,,
mondo:0700152,canine hepatocellular carcinoma,,,,,,,C129298,,,,,,
mondo:0700153,canine lung adenocarcinoma,,,,,,,C129299,,,,,,
mondo:0700154,canine rhabdomyosarcoma,,,,,,,C129300,,,,,,
mondo:0700155,canine thyroid adenocarcinoma,,,,,,,C132275,,,,,,
mondo:0700156,canine soft tissue sarcoma,,,,,,,C132276,,,,,,
mondo:0700157,canine oral squamous cell carcinoma,,,,,,,C132823,,,,,,
mondo:0700158,canine pancreatic carcinoma,,,,,,,C134944,,,,,,
mondo:0700159,canine acanthomatous epulis,,,,,,,C134956,,,,,,
mondo:0700160,canine mammary adenoma,,,,,,,C147073,,,,,,
mondo:0700161,canine gastrointestinal stromal tumor,,,,,,,C158783,,,,,,
mondo:0700162,canine granular cell tumor,,,,,,,C158784,,,,,,
mondo:0700163,canine Langerhans cell histiocytosis,,,,,,,C158785,,,,,,
mondo:0700164,canine nephroblastoma,,,,,,,C158786,,,,,,
mondo:0700165,canine thyroid gland medullary carcinoma,,,,,,,C161006,,,,,,
mondo:0700166,canine transmissible venereal tumor,,,,,,,C162473,,,,,,
mondo:0700167,canine sebaceous gland epithelioma,,,,,,,C176701,,,,,,
mondo:0700168,canine oral melanoma,,,,,,,C185639,,,,,,
mondo:0700169,canine cutaneous t-cell lymphoma,,,,,,,C186279,,,,,,
mondo:0700170,equine neoplasm,,,,,,,,,,,,,
mondo:0700171,horse melanoma,,,,,,,C134569,,,,,,
mondo:0700172,horse lymphoma,,,,,,,C134778,,,,,,
mondo:0700173,horse sarcoid,,,,,,,C134995,,,,,,
mondo:0700174,horse transitional cell carcinoma,,,,,,,C173624,,,,,,
mondo:0700175,feline neoplasm,,,,,,,,,,,,,
mondo:0700176,feline lymphoma,,,,,,,C132193,,,,,,
mondo:0700177,feline mammary carcinoma,,,,,,,C132274,,,,,,
mondo:0700178,feline oral squamous cell carcinoma,,,,,,,C132824,,,,,,
mondo:0700179,feline osteosarcoma,,,,,,,C132825,,,,,,
mondo:0700180,feline bronchioloalveolar lung carcinoma,,,,,,,C134559,,,,,,
mondo:0700181,feline fibrosarcoma,,,,,,,C134560,,,,,,
mondo:0700182,feline erythroleukemia,,,,,,,C134770,,,,,,
mondo:0700183,feline reticulum cell sarcoma,,,,,,,C135008,,,,,,
mondo:0700184,feline large granular lymphocyte lymphoma,,,,,,,C135724,,,,,,
mondo:0700185,feline melanoma,,,,,,,C156362,,,,,,
mondo:0700186,feline histiocytic sarcoma,,,,,,,C157503,,,,,,
mondo:0700187,feline progressive histiocytosis,,,,,,,C176702,,,,,,
mondo:0700188,feline synovial cell sarcoma,,,,,,,C181658,,,,,,
mondo:0700189,chicken neoplasm,,,,,,,C135005,,,,,,
mondo:0700190,chicken bursal lymphoma,,,,,,,C134556,,,,,,
mondo:0700191,chicken fibrosarcoma,,,,,,,C134557,,,,,,
mondo:0700192,chicken hepatoma,,,,,,,C134558,,,,,,
mondo:0700193,chicken monocytic leukemia,,,,,,,C134945,,,,,,
mondo:0700194,chicken lymphoma,,,,,,,C135004,,,,,,
mondo:0700195,rous sarcoma,,,,,,,C17466,,,,,,
mondo:0700196,fish melanoma,,,,,,,C135006,,,,,,
mondo:0700197,porcine leukemia,,,,,,,C141365,,,,,,
mondo:0700198,porcine lymphoma,,,,,,,C134786,,,,,,
mondo:0700199,sheep lung adenocarcinoma,,,,,,,C147532,,,,,,
mondo:0700200,atypical dopamine transporter deficiency syndrome,['atypical DTDS'],,,,,,,,,,,,
mondo:0700201,"tick-borne infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700202,"Bunyaviridae infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700203,"pestivirus infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700204,"trichostrongyloidiasis, non-human animal",,,,,,,,,,,,,
mondo:0700205,"ehrlichiosis, non-human animal",,,,,,,,,,,,,
mondo:0700206,"Parvoviridae infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700207,constitutional delay of growth and puberty,,,,,C0342538,,,,,,,,
mondo:0700208,"Caliciviridae infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700209,"Strongylida infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700210,"enterovirus infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700211,"Erysipelothrix infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700212,"tuberculosis, non-human animal",,,,,,,,,,,,,
mondo:0700213,"trypanosomiasis, non-human animal",,,,,,,,,,,,,
mondo:0700214,"Herpesviridae infectious disease, non-human animal",,,,,,,,,,,,,
mondo:0700215,NTRK fusion positive cancer,"['neurotrophic tyrosine receptor kinase fusion positive cancer', 'NTRK fusion positive solid tumour', 'NTRK fusion positive solid tumor', 'neurotrophic tyrosine receptor kinase fusion positive solid tumor', 'neurotrophic tyrosine receptor kinase fusion positive solid tumour', 'neurotrophic tyrosine receptor kinase fusion positive neoplasm', 'NTRK fusion positive neoplasm']",,,,,,,,,,,,
mondo:0700216,RET fusion positive cancer,"['RET fusion positive solid tumor', 'RET fusion positive solid tumour', 'RET fusion positive neoplasm']",,,,,,,,,,,,
mondo:0700217,neonatal sepsis,,,,,,,,,,,,,
mondo:0700218,group B streptococcal infection,,,,,,,C87168,,,,,,
mondo:0700219,neoplastic meningitis,"['leptomeningeal carcinomatosis', 'leptomeningeal metastasis', 'meningeal carcinomatosis', 'leptomeningeal carcinoma', 'carcinomatous meningitis', 'meningeal metastasis', 'metastatic malignant neoplasm in the leptomeninges']",,,,,,C3814,,,,,,
mondo:0700220,disease related to transplantation,,,,306644,C1998172,,,,,,,,
mondo:0700221,disease related to solid organ transplantation,,,,,,,,,,,,,
mondo:0700222,disease related to hematopoietic stem cell transplant,,,,,,,,,,,,,
mondo:0700223,hereditary skeletal muscle disorder,"['genetic muscular disease', 'genetic muscle disease', 'hereditary muscle disorder', 'genetic muscular disorder']",,,,,,,,,,,,
mondo:0700225,hereditary gallbladder disorder,,,,,,,,,,,,,
mondo:0700226,food allergy,"['food hypersensitivity', 'allergy of food material', 'food material allergic disease']",3044,,,,,,1001890,D005512,995.3,,,
mondo:0800001,"delayed sleep phase syndrome, susceptibility to","['delayed sleep phase disorder, susceptibility to']",,614163,,,,,,,,,,
mondo:0800025,Teebi hypertelorism syndrome 1,"['Teebi hypertelorism syndrome', 'hypertelorism, Teebi type', 'Brachycephalofrontonasal dysplasia', 'craniofrontonasal dysplasia, Teebi type', 'Teebi syndrome']",0080698,145420,1519,CN199596,"['0.002405', '0.0723', '0.003462', '-0.01471', '0.03244', '-0.0733', '-0.01003', '0.089', '-0.1102', '-0.03598', '-0.03088', '-0.006725', '0.03308', '0.01212', '-0.07007', '-0.01516', '0.003279', '-0.0406', '-0.003107', '-0.1055', '-0.02199', '-0.02715', '0.08795', '0.000328', '0.03122', '-0.01671', '-0.04468', '-0.02122', '0.04788', '-0.0496', '0.07275', '-0.01872', '0.08594', '0.0347', '0.0291', '-0.0545', '-0.05203', '-0.0537', '0.01449', '-0.113', '0.06415', '-0.0635', '0.02547', '-0.02528', '-0.009056', '-0.05988', '-0.006596', '0.1067', '0.001081', '0.005394', '-0.01407', '-0.03445', '0.00434', '0.008', '-0.02434', '-0.053', '0.02919', '-0.02425', '-0.07446', '0.004295', '0.03146', '0.003365', '-0.01418', '0.00721', '0.000991', '0.02995', '0.05762', '0.03986', '-0.05887', '0.09155', '-0.06396', '0.0403', '0.02176', '-0.06186', '0.01043', '0.04352', '-0.00307', '-0.04117', '-0.0682', '-0.04163', '0.003345', '-0.008194', '-0.05777', '0.078', '-0.02396', '0.01698', '0.0054', '0.0768', '0.0927', '0.03467', '0.00743', '0.1015', '0.05276', '0.01646', '0.166', '0.02939', '0.05862', '-0.1025', '0.02342', '0.05762']",,,,,,,
mondo:0800026,"central hypoventilation syndrome, congenital, 1, with or without Hirschsprung disease","['congenital central alveolar hypoventilation syndrome', 'Ondine^s curse (formerly)', 'CCHS', 'CCHS with Hirschsprung disease', 'Ondine syndrome', 'Haddad syndrome', 'autonomic control, congenital failure of', 'central hypoventilation syndrome, congenital', 'primary alveolar hypoventilation', 'idiopathic congenital central alveolar hypoventilation', 'Ondine curse', 'congenital Ondine curse', 'Ondine curse (formerly)', 'congenital central hypoventilation', 'congenital failure of autonomic control', 'Ondine-Hirschsprung disease', 'central congenital hypoventilation syndrome', 'Ondine curse, congenital']",0060731,209880,661,C1275808,"['-0.00729', '0.078', '0.01117', '-0.02065', '0.0207', '-0.0894', '0.01733', '0.0535', '-0.03326', '-0.0499', '-0.001072', '-0.01223', '-0.01657', '0.01862', '-0.0284', '-0.0629', '-0.009346', '-0.0429', '-0.01599', '-0.1062', '-0.01692', '-0.02798', '0.04913', '-0.04544', '0.02731', '-0.0137', '-0.04294', '-0.03015', '0.02565', '-0.04742', '0.0567', '0.002068', '0.07983', '0.03046', '0.03217', '-0.0336', '-0.00633', '-0.03937', '-0.02438', '-0.076', '0.01159', '-0.05518', '0.01701', '-0.0422', '0.011734', '-0.0699', '-0.0137', '0.06683', '0.01224', '0.03632', '-0.01268', '0.002522', '-0.01266', '-0.009384', '-0.0357', '-0.006813', '0.066', '-0.03044', '-0.0919', '0.00734', '0.04276', '0.04126', '0.00989', '0.02339', '0.02028', '0.00916', '0.0844', '0.03265', '-0.0668', '0.0928', '-0.06635', '0.00975', '0.02144', '-0.05035', '0.01714', '0.0209', '0.01299', '-0.00494', '-0.06207', '-0.05652', '0.01014', '0.005512', '-0.0481', '0.0547', '0.00797', '-0.02225', '0.02165', '0.0653', '0.0718', '0.01695', '0.02457', '0.0518', '0.02121', '0.02768', '0.1251', '0.01994', '0.0548', '-0.1064', '-0.0196', '0.02934']",C98889,,,,G47.3,10066131,
mondo:0800027,"leukoencephalopathy, diffuse hereditary, with spheroids 1","['ALSP', 'leukoencephalopathy with neuroaxonal spheroids, autosomal dominant', 'leukoencephalopathy, hereditary diffuse, with spheroids', 'gliosis, familial progressive subcortical', 'HDLS', 'dementia, familial, Neumann type', 'familial progressive subcortical gliosis', 'subcortical gliosis of Neumann', 'adult-onset leukoencephalopathy with axonal spheroids and pigmented glia', 'neuroaxonal leukodystrophy', 'familial dementia, Neumann type', 'hereditary diffuse leukoencephalopathy with axonal spheroids', 'FPSG', 'autosomal dominant leukoencephalopathy with neuroaxonal spheroids', 'hereditary diffuse leukoencephalopathy with spheroids', 'POLD', 'leukoencephalopathy, adult-onset, with axonal spheroids and pigmented glia', 'pigmentary orthochromatic leukodystrophy', 'GPSC', 'adult-onset leukodystrophy with neuroaxonal spheroids', 'leukoencephalopathy, diffuse hereditary, with spheroids']",0080523,221820,313808,C3711381,"['-0.0984', '0.1578', '0.0723', '-0.06247', '-0.02005', '-0.1664', '-0.05536', '0.0754', '-0.1159', '0.1238', '-0.0643', '0.0292', '-0.04764', '-0.0919', '0.02885', '-0.0692', '0.04892', '-0.0965', '0.0008855', '-0.255', '-0.0143', '-0.14', '0.05286', '0.039', '-0.01444', '0.0296', '-0.04123', '-0.0578', '0.004402', '-0.1302', '0.12115', '0.02182', '0.1305', '-0.02774', '0.0949', '-0.07275', '-0.1103', '-0.08984', '-0.02127', '-0.1178', '0.0649', '-0.1984', '0.02196', '-0.03558', '0.001841', '-0.09955', '-0.05313', '0.0696', '-0.05222', '-0.0489', '0.0729', '0.06174', '-0.007515', '0.01259', '-0.1007', '-0.02713', '0.2119', '-0.0702', '-0.2416', '0.02274', '0.0468', '0.00926', '0.0439', '0.03412', '-0.0206', '0.006943', '0.2211', '0.2333', '-0.07117', '0.1786', '-0.0952', '0.02184', '0.0839', '-0.1056', '0.1328', '0.04105', '-0.002481', '0.07184', '-0.04324', '-0.1393', '-0.006153', '-0.05493', '-0.02559', '0.197', '-0.05734', '-0.0487', '0.01637', '0.1438', '0.06744', '-0.0315', '0.2386', '0.10834', '0.1185', '0.07166', '0.2844', '0.07385', '0.1729', '-0.11664', '-0.03897', '0.1152']",C153289,,C580150,323.81,,,
mondo:0800028,"dyskinesia with orofacial involvement, autosomal dominant","['FDFM', 'dyskinesia, familial, with facial myokymia', 'ADCY5-related dyskinesia']",,606703,324588,C1847627,"['-0.03342', '0.1324', '0.04626', '-0.1088', '-0.02492', '-0.12274', '0.0843', '0.1157', '-0.09076', '-0.02484', '-0.02866', '0.00851', '-0.02744', '0.002432', '-0.01898', '-0.01408', '-0.00991', '-0.0985', '-0.013985', '-0.2488', '0.0346', '0.02107', '0.0687', '-0.03061', '0.03186', '0.01542', '0.005817', '-0.1026', '0.003664', '-0.02887', '0.07385', '0.04404', '0.1268', '0.04575', '0.01843', '-0.0014515', '-0.03174', '-0.05432', '-0.04608', '-0.10645', '0.08777', '-0.1654', '0.02397', '-0.03674', '0.0541', '-0.0777', '-0.07495', '0.1509', '-0.001016', '0.0961', '-0.04135', '0.06635', '0.00972', '-0.02827', '-0.02864', '-0.05078', '0.1262', '-0.0937', '-0.10114', '0.013664', '0.1075', '0.05328', '-0.00825', '-0.003569', '-0.0615', '0.02095', '0.1483', '0.1067', '-0.0855', '0.145', '-0.0519', '0.03476', '0.04083', '-0.10315', '0.04468', '0.08875', '0.0818', '0.005848', '-0.11017', '-0.04797', '0.03123', '0.04916', '0.01666', '0.1409', '-0.01475', '0.02599', '-0.003685', '0.1076', '0.1399', '0.03043', '0.04544', '0.05905', '0.0487', '0.0828', '0.2412', '0.0659', '0.11084', '-0.104', '-0.04303', '0.05734']",,,C564676,,G51.4,,
mondo:0800029,interstitial lung disease 2,"['IPF', 'CFA', 'interstitial pneumonitis, usual', 'pulmonary fibrosis, idiopathic', 'usual interstitial pneumonia', 'cryptogenic fibrosing alveolitis', 'fibrosing alveolitis', 'fibrosing alveolitis, cryptogenic', 'UIP', 'Hamman-rich disease', 'familial idiopathic pulmonary fibrosis', 'ILD2', 'fibrocystic pulmonary dysplasia', 'idiopathic pulmonary fibrosis, familial']",0050156,178500,79126,,"['-0.01193', '0.09607', '-0.00737', '-0.04953', '0.02003', '-0.095', '0.0519', '0.117', '-0.0879', '0.003094', '-0.0473', '-0.0485', '-0.0695', '0.02391', '-0.009796', '-0.1305', '0.011', '0.005676', '-0.03476', '-0.1854', '0.0406', '-0.05453', '0.1143', '-0.1163', '0.00826', '-0.02272', '0.0415', '0.0385', '0.01778', '-0.0616', '0.1206', '-0.0853', '0.1769', '0.01092', '0.0798', '-0.0843', '-0.05307', '-0.04736', '0.004047', '-0.06198', '0.03513', '-0.04147', '0.0696', '0.003614', '-0.001074', '-0.0576', '-0.04608', '0.10077', '-0.01736', '0.03647', '-0.05023', '-0.015335', '0.08997', '0.04324', '-0.05542', '-0.0234', '0.0657', '-0.08594', '-0.1582', '-0.006046', '0.07947', '0.01584', '-0.02261', '0.01958', '0.01613', '-0.02141', '0.1249', '0.08276', '-0.1155', '0.1482', '-0.12396', '-0.02405', '0.11194', '-0.04218', '0.02782', '0.03976', '0.01548', '-0.002792', '-0.0483', '-0.08154', '-0.02364', '0.01624', '-0.03873', '0.0576', '-0.0438', '-0.005894', '0.1244', '0.0927', '0.0927', '-0.011665', '0.03397', '0.05606', '-0.06555', '0.03787', '0.2404', '0.0857', '0.1324', '-0.12036', '-0.10156', '0.02982']",C35716,0000768,D054990,516.31,J84.112,10021240,
mondo:0800030,gastrointestinal defects and immunodeficiency syndrome 1,"['combined immunodeficiency-enteropathy spectrum', 'CID-MIA/early-onset IBD', 'MINAT', 'multiple intestinal atresia and/or inflammatory bowel disease with or without immunodeficiency', 'intestinal atresia, multiple', 'familial intestinal polyatresia syndrome', 'FIPA']",,243150,436252,,,,,,,,,
mondo:0800031,"central hypoventilation syndrome, congenital",,,,,,,,,,,,,
mondo:0800032,MELAS syndrome caused by mutation in MTTL1,['MTTL1 MELAS syndrome'],,,,,,,,,,,,
mondo:0800033,MELAS syndrome caused by mutation in MTTQ,['MTTQ MELAS syndrome'],,,,,,,,,,,,
mondo:0800034,MELAS syndrome caused by mutation in MTTH,['MTTH MELAS syndrome'],,,,,,,,,,,,
mondo:0800035,MELAS syndrome caused by mutation in MTTK,['MTTK MELAS syndrome'],,,,,,,,,,,,
mondo:0800036,MELAS syndrome caused by mutation in MTTC,['MTTC MELAS syndrome'],,,,,,,,,,,,
mondo:0800037,MELAS syndrome caused by mutation in MTTS1,['MTTS1 MELAS syndrome'],,,,,,,,,,,,
mondo:0800038,MELAS syndrome caused by mutation in MTND1,['MTND1 MELAS syndrome'],,,,,,,,,,,,
mondo:0800039,MELAS syndrome caused by mutation in MTND5,['MTND5 MELAS syndrome'],,,,,,,,,,,,
mondo:0800040,MELAS syndrome caused by mutation in MTND6,['MTND6 MELAS syndrome'],,,,,,,,,,,,
mondo:0800041,MELAS syndrome caused by mutation in MTTS2,['MTTS2 MELAS syndrome'],,,,,,,,,,,,
mondo:0800042,restrictive dermopathy 1,"['tight skin contracture syndrome', 'restrictive dermopathy', 'tight skin contracture syndrome, lethal', 'restrictive dermopathy 1, lethal', 'restrictive dermopathy, lethal', 'foetal hypokinesia sequence due to restrictive dermopathy', 'lethal restrictive dermopathy', 'fetal hypokinesia sequence due to restrictive dermopathy', 'hyperkeratosis-contracture syndrome']",0070369,275210,1662,C0406585,"['-0.5557', '0.1346', '-0.1004', '-0.1324', '0.1272', '-0.275', '-0.01364', '0.5625', '-0.412', '-0.3477', '0.1366', '-0.4915', '-0.2042', '-0.2817', '-0.6646', '0.0983', '0.6973', '-0.2751', '-0.0607', '-0.6167', '-0.1837', '-0.00833', '0.698', '-0.5723', '-0.03555', '-0.2517', '-0.09064', '0.239', '0.6846', '-0.647', '0.4587', '0.0997', '0.6895', '0.3167', '-0.01703', '0.2686', '0.1912', '-0.1991', '0.1307', '0.1519', '0.010414', '0.1425', '-0.2266', '-0.0645', '0.11664', '-0.1882', '-0.1542', '0.7266', '-0.454', '0.529', '-0.576', '-0.5767', '0.557', '0.2185', '-0.533', '-0.3774', '0.317', '0.6147', '0.4307', '-0.1951', '0.4229', '0.2085', '-0.3225', '0.2544', '-0.2693', '-0.7773', '0.631', '0.06793', '-0.596', '0.9585', '-0.01772', '-0.005615', '0.792', '0.1043', '-0.5176', '-0.3318', '0.2444', '-0.594', '-0.4224', '-0.0603', '0.005943', '0.00824', '0.601', '0.244', '-0.683', '-0.077', '-0.1497', '0.4001', '0.227', '-0.3022', '0.2756', '-0.2021', '0.4248', '0.2124', '0.06113', '0.3767', '0.5483', '-0.4673', '0.567', '-0.05783']",,,C536920,,,,
mondo:0800043,Stüve-Wiedemann syndrome 1,"['Stuve-Wiedemann syndrome/Schwartz-Jampel type 2 syndrome', 'Stws', 'STWS', 'Stuve-Wiedemann/Schwartz-Jampel type 2 syndrome', 'neonatal Schwartz-Jampel syndrome', 'SWS', 'Stüve-Wiedemann/Schwartz-Jampel type 2 syndrome', 'STUVE-Wiedemann syndrome', 'Stüve-Wiedemann syndrome', 'Schwartz-Jampel syndrome type 2', 'Schwartz-Jampel syndrome neonatal', 'SJS2', 'Stüve-Wiedemann dysplasia', 'Schwartz-Jampel syndrome, type 2', 'neonatal Schwartz-Jampel syndrome type 2', 'Schwartz-Jampel syndrome, neonatal']",,601559,3206,C0796176,"['-0.03069', '0.015396', '-0.334', '-0.3027', '-0.2478', '-0.475', '0.5205', '1.227', '-0.446', '-0.5996', '-0.07556', '0.03796', '-0.1367', '0.0338', '-0.05328', '0.556', '0.504', '-0.0148', '-0.3528', '-0.274', '-0.06076', '-0.1353', '0.2935', '-0.4004', '-0.4622', '-0.4219', '-0.2445', '-0.0668', '-0.134', '-0.533', '0.3918', '-0.2966', '-0.04544', '0.1794', '-0.5864', '-0.1462', '0.2422', '-0.6045', '-0.2008', '0.2268', '-0.1985', '0.06247', '0.11865', '-0.09705', '-0.007458', '0.1696', '-0.774', '0.3281', '0.1437', '0.685', '-0.5464', '-0.2123', '0.012314', '0.2595', '-0.2123', '-0.238', '-0.518', '-0.0559', '0.431', '-0.03108', '0.3608', '0.063', '-0.1118', '-0.1913', '-0.5444', '-0.2184', '0.2646', '0.7188', '-0.4055', '0.536', '-0.4658', '-0.1227', '-0.0629', '-0.0368', '-0.0695', '0.3806', '0.3374', '-0.1387', '0.2239', '0.567', '-0.3828', '-0.2418', '0.2996', '0.8496', '-0.6177', '0.4558', '0.1298', '0.1857', '0.03052', '-0.443', '-0.1656', '0.11584', '-0.343', '0.3313', '0.4785', '0.433', '0.7935', '-0.5366', '0.2974', '0.297']",,,C537502,,,,
mondo:0800044,congenital disorder of deglycosylation 1,"['CDDG', 'CDG IV', 'NGLY1 deficiency', 'congenital disorder of glycosylation type IV', 'NGLY1-CDDG', 'CDG IV, formerly', 'deficiency of N-glycanase 1', 'CDG1V', 'congenital disorder of deglycosylation', 'congenital disorder of deglycosylation;CDDG', 'congenital disorder of glycosylation, type IV, formerly', 'congenital disorder of glycosylation, type IV', 'alacrimia - choreoathetosis - liver dysfunction syndrome', 'congenital disorder of deglycosylation 1']",0060728,615273,404454,C3808991,"['-0.5054', '0.5527', '0.10175', '-0.2122', '-0.00249', '0.00813', '-0.2233', '0.4155', '-0.722', '0.1948', '-0.424', '-0.3342', '-0.02655', '-0.1406', '0.1287', '-0.10077', '0.079', '0.01648', '-0.0574', '-0.882', '0.2854', '-0.6226', '0.02515', '0.0881', '0.3472', '-0.2656', '-0.1699', '0.10114', '-0.1069', '0.1799', '0.4482', '0.403', '0.4995', '-0.05212', '-0.01297', '0.1489', '-0.1437', '-0.334', '0.0834', '-0.414', '0.001559', '-0.2383', '-0.3462', '0.659', '-0.2961', '-0.6367', '0.4548', '-0.4482', '0.03069', '0.3882', '-0.2103', '0.2373', '-0.137', '-0.281', '0.395', '-0.2563', '-0.0075', '0.6426', '-0.2961', '0.1126', '0.1847', '0.1188', '0.419', '-0.1396', '-0.2844', '-0.1543', '0.314', '0.2634', '-0.5625', '-0.2715', '-0.4976', '0.2175', '-0.1864', '0.2427', '0.1017', '-0.149', '0.4275', '0.309', '-0.0656', '-0.2773', '0.06055', '-0.1222', '-0.113', '-0.04108', '-0.252', '-0.1343', '0.175', '0.489', '0.44', '0.6523', '0.163', '0.554', '-0.273', '-0.07465', '0.713', '0.8306', '0.02715', '0.157', '0.3633', '0.2115']",C126746,,,,,,
mondo:0800045,"autoinflammatory syndrome, familial, Behcet-like 1","['Behçet-like disease due to haploinsufficiency of A20', 'AISBL', 'autoinflammatory syndrome, familial, Behcet-like 1', 'hereditary paediatric Behçet-like disease', 'autoinflammatory syndrome, familial, Behcet-like', 'Behçet-like disease due to HA20', 'hereditary pediatric Behçet-like disease']",0080944,616744,476102,C4225218,,,,,,,,
mondo:0800046,"thyroid hormone metabolism, abnormal 1","['THMA1', 'short stature-delayed bone age due to thyroid hormone metabolism deficiency', 'thyroid hormone metabolism, abnormal']",,609698,171706,C1864761,"['-0.401', '0.0672', '0.1974', '-0.1812', '0.1323', '0.1539', '-0.009224', '0.8193', '-0.1309', '-0.1748', '0.041', '0.175', '0.1793', '-0.0876', '0.1587', '-0.1763', '0.289', '0.01558', '-0.4678', '-0.682', '0.1866', '-0.1912', '0.2335', '-0.1066', '0.1705', '-0.0701', '0.1616', '-0.2347', '-0.08344', '-0.387', '0.2607', '-0.0444', '0.4504', '0.4382', '-0.2358', '-0.12115', '-0.0983', '-0.10986', '-0.0718', '-0.1497', '0.0642', '0.02823', '0.1362', '-0.1141', '-0.1371', '-0.3389', '0.453', '0.1895', '0.03738', '0.1368', '-0.2223', '0.1456', '0.1859', '-0.006657', '-0.417', '0.0876', '0.01927', '-0.5566', '0.01637', '0.12213', '0.2703', '0.2668', '-0.1384', '-0.496', '-0.0651', '-0.003883', '0.15', '0.5234', '-0.549', '-0.1114', '0.05765', '0.2659', '0.03778', '-0.4255', '0.2146', '0.004208', '0.02557', '-0.3293', '-0.1857', '0.2222', '-0.04935', '0.3005', '-0.099', '0.1973', '-0.04904', '0.2988', '0.091', '-0.1687', '0.6416', '0.11743', '0.0518', '0.5713', '-0.0895', '-0.2837', '0.398', '0.0742', '0.2603', '-0.1252', '0.0853', '0.288']",,,C566454,,,,
mondo:0800047,"macrothrombocytopenia, isolated, 1, autosomal dominant","['autosomal dominant macrothrombocytopenia TUBB1-related', 'TUBB1 autosomal dominant macrothrombocytopenia', 'MACTHC1', 'autosomal dominant macrothrombocytopenia caused by mutation in TUBB1', 'macrothrombocytopenia, autosomal dominant, TUBB1-related']",0090102,613112,,C2751259,,,,C567747,,,,
mondo:0800063,primordial dwarfism and slender bone disorder,,,,,,,,,,,,,
mondo:0800064,osteogenesis imperfecta and a reduction of bone mineral density.,,,,,,,,,,,,,0004349
mondo:0800066,polydactyly-syndactyly-triphalangism,,,,,,,,,,,,,
mondo:0800075,dysostosis with predominant vertebral with and without costal involvement,,,,93454,,,,,,,,,
mondo:0800080,severe spondylodysplastic dysplasia,,,,,,,,,,,,,
mondo:0800084,primary bone dysplasia with increased bone density,"['sclerosing bone dysplasia', 'primary skeletal dysplasia with increased bone density', 'primary osteodysplasia with increased bone density']",,,93444,CN043667,,,,,,,,
mondo:0800085,dysostosis with predominant craniofacial involvement,,,,93453,,,,,,,,,
mondo:0800086,primary bone dysplasia with multiple joint dislocations,"['primary osteodysplasia with multiple joint dislocations', 'primary skeletal dysplasia with multiple joint dislocations']",,,93441,,,,,,,,,
mondo:0800087,type 11 collagen-related bone disorder,,,,93422,,,,,,,,,
mondo:0800088,lysosomal storage disease with skeletal involvement,['dysostosis multiplex'],,,93448,CN206618,,,,,756.9,,,
mondo:0800089,primary bone dysplasia with disorganized development of skeletal components,"['primary skeletal dysplasia with disorganised development of skeletal components', 'primary skeletal dysplasia with disorganized development of skeletal components', 'primary osteodysplasia with disorganized development of skeletal components', 'primary osteodysplasia with disorganised development of skeletal components']",,,93450,,,,,,,,,
mondo:0800090,ectrodactyly with and without other manifestations,,,,498477,,,,,,,,,
mondo:0800091,overgrowth or tall stature syndrome with skeletal involvement,,,,498448,,,,,,,,,
mondo:0800092,hereditary inflammatory or rheumatoid-like osteoarthropathy,['genetic inflammatory or rheumatoid-like osteoarthropathy'],,,498445,,,,,,,,,
mondo:0800093,dysostosis with brachydactyly without extraskeletal manifestations,,,,498451,,,,,,,,,
mondo:0800094,dysostosis with brachydactyly with extraskeletal manifestations,,,,498454,,,,,,,,,
mondo:0800095,syndrome with synostosis or other joint formation defect,,,,93459,CN206620,,,,,,,,
mondo:0800096,abnormal mineralization disorder,"['disorder of bone mineralization', 'osteomalacia']",,,,,,,,,,,,
mondo:0800098,SNRNP200-related dominant retinopathy,"['SNRNP200 retinitis pigmentosa', 'retinitis pigmentosa 33', 'RP 33', 'SNRNP200-related dominant retinopathy', 'retinitis pigmentosa caused by mutation in SNRNP200', 'retinitis pigmentosa type 33', 'RP33']",,,,,,,,,,,,
mondo:0800099,RDH12-related recessive retinopathy,"['retinitis pigmentosa 53', 'RDH12-related recessive retinopathy', 'Leber congenital amaurosis type 13', 'RDH12 Leber congenital amaurosis', 'Leber congenital amaurosis caused by mutation in RDH12', 'LCA13', 'Leber congenital amaurosis 13']",,,,,,,,,,,,
mondo:0800100,RDH12-related dominant retinopathy,['RDH12-related dominant retinopathy'],,,,,,,,,,,,
mondo:0800101,NMNAT1-related retinopathy,"['NMNAT1-related retinopathy', 'NMNAT1 Leber congenital amaurosis', 'SHILCA', 'Leber congenital amaurosis type 9', 'amaurosis congenita of Leber, type 9', 'LCA9', 'spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis', 'Leber congenital amaurosis 9', 'Leber congenital amaurosis caused by mutation in NMNAT1', 'SHILCA Syndrome']",,,,,,,,,,,,
mondo:0800102,CNGA3-related retinopathy,"['colorblindness, total', 'achromatopsia caused by mutation in CNGA3', 'achromatopsia 2', 'CNGA3-related retinopathy', 'RMCH2', 'CNGA3 achromatopsia', 'rod monochromatism 2', 'rod monochromacy 2', 'ACHM2', 'achromatopsia type 2']",,,,,,,,,,,,
mondo:0800103,COACH syndrome 1,"['cerebellar vermis hypo/aplasia, oligophrenia, congenital ataxia, ocular coloboma, and hepatic fibrosis']",,216360,,,,,,,,,,
mondo:0800104,immunodeficiency 105,"['SCID, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive', 'IMD105', 'severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive']",,619924,,,,,,,,,,
mondo:0800105,catatonia,,,,,,,,,D002389,,,,
mondo:0800106,disruptive behavior disorder,['disruptive disorder'],,,,,,C99753,,,,,,
mondo:0800107,anterior deviation infundibular septum,,,,,756812,,,,,,,,
mondo:0800108,cleft leaflet of tricuspid valve,['cleft tricuspid valve'],,,,576470,,,,,,,,
mondo:0800109,persistent tachypnoe of infancy,['PTI'],,,,,,,,,,,,
mondo:0800110,"persistent tachypnoe of infancy, aberrant","['PTI, aberrant']",,,,,,,,,,,,
mondo:0800111,"persistent tachypnoe of infancy, usual","['PTI, usual']",,,,,,,,,,,,
mondo:0800112,non-atopic asthma,"['instrinsic asthma', 'non-allergic asthma']",,,,,,,,,,,,
mondo:0800113,necrotizing vasculitis,['systemic vasculitis'],,,,,,C70635,,,,,,
mondo:0800114,follicular bronchiolits,,,,,,,,,,,,,
mondo:0800117,cutaneous botryomycosis,,,,,,,,,,,,,
mondo:0800118,visceral botryomycosis,['pulmonary botromycosis'],,,,,,,,,,,,
mondo:0800119,postinfectious bronchiolitis obliterans,['PIBO'],,,,,,,,,,,,
mondo:0800120,Mac-Leod-Swyer-James-Syndrome,"['SJS', 'Swyer-James-(Macleod)-Syndrome']",,,,,,,,,,,,
mondo:0800121,cellular interstitial pneumonitis,,,,,,,,,,,,,
mondo:0800123,bronchiolocentric pattern of interstitial pneumonia,['BPIP'],,,,,,,,,,,,
mondo:0800124,Lane Hamilton syndrome,,,,,,,,,,,,,
mondo:0800125,disseminated visceral giant cell angiitis,"['disseminated visceral giant cell arteristic', 'disseminated visceral giant cell arteritis']",,,,,,,,,,,,
mondo:0800126,dystrophic pulmonary ossification,,,,,,,,,,,,,
mondo:0800127,pulmonary amyloidosis,,,,,,,,,,,,,
mondo:0800128,combined immunodeficiency due to POLE2 deficiency,,,,,,,,,,,,,
mondo:0800129,"autoinflammatory disease, X-linked","['NEMO deleted exon 5 syndrome', 'autoinflammatory syndrome, X-linked']",,301081,,,,,,,,,,
mondo:0800130,autoinflammatory syndrome with immunodeficiency,,,619375,,,,,,,,,,
mondo:0800131,"hyper-IgE recurrent infection syndrome 4A, autosomal dominant",,,619752,,,,,,,,,,
mondo:0800132,autoinflammatory-pancytopenia syndrome due to DNASE2 deficiency,,,619858,,,,,,,,,,
mondo:0800133,pulmonary hypoplasia,,,,,,,C99035,,,,,,
mondo:0800134,primary immunodeficiency due to calcium channel deficiency,,,,,,,,,,,,,
mondo:0800135,congenital emphysematous lung disease due to Filamin A loss-of-function variant,,,,,,,,,,,,,
mondo:0800136,non-severe combined immunodeficiency due to COPG1 deficiency,,,,,,,,,,,,,
mondo:0800137,early-onset pulmonary and cutaneous vasculitis,,,,,,,,,,,,,
mondo:0800138,multisystem autoimmune disease due to IKAROS gain of function,,,,,,,,,,,,,
mondo:0800139,HELIOS deficiency,,,,,,,,,,,,,
mondo:0800140,ITPKB deficiency,,,,,,,,,,,,,
mondo:0800141,MAN2B2 deficiency,,,,,,,,,,,,,
mondo:0800142,chronic mucocutaneous candidiasis and connective tissue disease due to JNK1 haploinsufficiency,['JNK1 haploinsufficiency (causing combination of chronic mucocutaneous candidiasis and connective tissue disease)'],,,,,,,,,,,,
mondo:0800143,cytomegalovirus pneumonia due to NOS2 deficiency,,,,,,,,,,,,,
mondo:0800144,autoimmune pulmonary disease due to PD-1 deficiency,,,,,,,,,,,,,
mondo:0800145,non-severe combined immunodeficiency due to polymerase delta deficiency,,,,,,,,,,,,,
mondo:0800146,"agammaglobulinemia, autosomal recessive, due to BOB1 deficiency",,,,,,,,,,,,,
mondo:0800147,hemophagocytic lymphohistiocytosis due to RhoG deficiency,,,,,,,,,,,,,
mondo:0800148,autoinflammatory syndrome due to TBK1 deficiency,,,,,,,,,,,,,
mondo:0800149,"immunodeficiency, common variable, due to APRIL deficiency",,,,,,,,,,,,,
mondo:0800152,disorder of galactose and fructose metabolism,,,,,,,,,,,,,
mondo:0800153,urea cycle disorder or inherited hyperammonemia,,,,,,,,,,,,,
mondo:0800154,inborn disorder of the metabolism of sulfur-containing amino acids and hydrogen sulfide,,,,,,,,,,,,,
mondo:0800155,inborn disorder of glycine and serine metabolism,,,,,,,,,,,,,
mondo:0800156,"inborn disorder of ornithine, proline and hydroxyproline metabolism",,,,,,,,,,,,,
mondo:0800157,"inborn disorder of lysine, hydroxylysine, and tryptophan metabolism",,,,,,,,,,,,,
mondo:0800158,inborn disorder of glutamate/glutamine and aspartate/asparagine metabolism,,,,,,,,,,,,,
mondo:0800159,disorder of polyamine metabolism,,,,,,,,,,,,,
mondo:0800166,Knobloch syndrome,,,,,,,,,,,,,
mondo:0800167,Knobloch syndrome 1,"['retinal detachment and occipital encephalocele', 'KNOBLOCH syndrome 1', 'Knobloch syndrome, type 1', 'retinal detachment-occipital encephalocele syndrome', 'myopia retinal detachment encephalocele', 'Knobloch-Layer syndrome', 'KNO', 'KNO1', 'Knobloch syndrome type 1']",,267750,1571,C1849409,"['-0.1019', '-0.4175', '0.2151', '0.4365', '0.1345', '-0.6123', '0.306', '0.3416', '-0.4126', '-0.2927', '-0.3035', '-0.2286', '-0.1315', '-0.071', '-0.0922', '0.2169', '0.005013', '0.0799', '-0.2462', '-0.3867', '-0.01305', '0.4426', '-0.2642', '0.1442', '-0.11975', '-0.3733', '-0.1489', '0.06226', '0.652', '0.00381', '0.7812', '-0.404', '0.2788', '-0.2456', '0.1442', '0.35', '-0.4246', '-0.359', '-0.1542', '-0.7393', '0.1693', '-0.2615', '0.5', '-0.3467', '0.4465', '0.4116', '-0.2646', '-0.08923', '-0.3381', '-0.6787', '0.3562', '-0.08496', '0.0911', '0.1943', '-0.1351', '-0.1671', '0.2695', '0.3828', '-0.2407', '0.1586', '0.4707', '0.1948', '-0.1995', '0.4878', '0.01976', '-0.2067', '0.743', '0.02519', '-0.406', '0.3394', '-0.7754', '-0.009705', '-0.3733', '0.624', '-0.09595', '0.3618', '0.421', '-0.1815', '-0.3335', '0.007767', '0.1703', '0.3723', '0.1293', '1.249', '-0.4822', '0.03824', '0.3704', '0.7827', '-0.1403', '-0.1038', '-0.1957', '0.934', '0.3303', '0.0797', '0.62', '-0.0678', '0.784', '-0.4146', '0.1702', '0.10284']",,,C537209,759.89,,,
mondo:0800174,"encephalitis, acute, infection-induced, susceptibility to",,,,,,,,,,,,,
mondo:0800175,cardiogenic shock,,,,97292,C0036980,,,,,,R57.0,10007625,
mondo:0800176,black widow spider envenomation,"['black widow envenomation', 'poisoning caused by black widow venom', 'latrodectism', 'poisoning due to black widow spider', 'toxic effect of venom of black widow']",,,,,,,,,,,,
mondo:0800177,frostbite,,,,,,,C34627,0009527,,,,,
mondo:0800178,platinum-induced ototoxicity,"['deafness, platinum-induced', 'platinum-related ototoxicity']",,,,,,,,,,,,
mondo:0800179,periprosthetic joint infection,,,,,,,,,,,,,
mondo:0800180,CPOX-related hereditary coproporphyria,,,,,,,,,,,,,
mondo:0800181,OPA1-related optic atrophy with or without extraocular features,,,,,,,,,,,,,
mondo:0800182,TEK-related primary glaucoma,,,,,,,,,,,,,
mondo:0800183,PAX6-related ocular dysgenesis,,,,,,,,,,,,,
mondo:0800187,"immunodeficiency 83, susceptibility to viral infections",['IMD83'],,613002,,,,,,,,,,
mondo:0800188,"malignant hyperthermia, susceptibility to",,,,,,,,,,,,,
mondo:0800195,achalasia-alacrima syndrome,['AAAS'],,,,,,,,,,,,
mondo:0800196,achromatopsia 5,['ACHM5'],,,,,,,,,,,,
mondo:0800197,achromatopsia 6,['ACHM6'],,,,,,,,,,,,
mondo:0800198,alopecia universalis,['AU'],,,,,,,,,,,,
mondo:0800199,Angelman syndrome chromosome region,['ANCR'],,,,,,,,,,,,
mondo:0800200,"arthrogryposis, distal, type 2B4",['DA2B4'],,,,,,,,,,,,
mondo:0800201,"baldness, male pattern",['MPB'],,,,,,,,,,,,
mondo:0800204,calvarial doughnut lesions with bone fragility and spondylometaphyseal dysplasia,['CDLSMD'],,,,,,,,,,,,
mondo:0800206,epidermolysis bullosa dystrophica with subcorneal cleavage,['EBDSC'],,,,,,,,,,,,
mondo:0800207,"neuropathy, small fiber",['SFNP'],,,,,,,,,,,,
mondo:0800209,"fibrosis of extraocular muscles, congenital, 3b",['CFEOM3B'],,,,,,,,,,,,
mondo:0800210,"glaucoma 1, open angle, l",['GLC1L'],,,,,,,,,,,,
mondo:0800215,"multicentric Castleman disease, susceptibility to",['MCD'],,,,,,,,,,,,
mondo:0800222,"pelvic organ prolapse, susceptibility to, 1",['PVOP1'],,,,,,,,,,,,
mondo:0800224,"amyotrophic lateral sclerosis, susceptibility to, 13",['ALS13'],,,,,,,,,,,,
mondo:0800226,"strabismus, susceptibility to, 1",['STBMS1'],,,,,,,,,,,,
mondo:0800250,"Graves disease, susceptibility to, X-linked 2",['GRDX2'],,,,,,,,,,,,
mondo:0800261,"autoimmune thyroid disease, susceptibility to, 5",['AITD5'],,,,,,,,,,,,
mondo:0800268,"atrioventricular septal defect, susceptibility to, 1","['AVC defect', 'endocardial cushion defect', 'atrioventricular septal defect', 'atrioventricular canal defect', 'AVSD', 'AVSD1']",,,,,,,,,,,,
mondo:0800271,"epilepsy, juvenile myoclonic, susceptibility to, 6",['EJM6'],,,,,,,,,,,,
mondo:0800274,"autoimmune disease, susceptibility to, 5",['AIS5'],,,,,,,,,,,,
mondo:0800275,"autism, susceptibility to, 14a",['AUTS14A'],,,,,,,,,,,,
mondo:0800279,"epilepsy, idiopathic generalized, susceptibility to, 6",['EIG6'],,,,,,,,,,,,
mondo:0800287,"autism, susceptibility to, 14b",['AUTS14B'],,,,,,,,,,,,
mondo:0800290,Li-fraumeni-like syndrome,['LFL'],,,,,,,,,,,,
mondo:0800291,"crossed polydactyly, type I",['CP1'],,,,,,,,,,,,
mondo:0800294,progressive encephalomyelitis with rigidity,['PERM'],,,,,,,,,,,,
mondo:0800296,"microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 2",['MRCS2'],,,,,,,,,,,,
mondo:0800297,"neuronal ceroid lipofuscinosis, late infantile",['LINCL'],,,,,,,,,,,,
mondo:0800298,"peroxisome biogenesis disorder, complementation group 2",['CG2'],,,,,,,,,,,,
mondo:0800299,"myopathy, congenital, with excess of muscle spindles",['CMEMS'],,,,,,,,,,,,
mondo:0800300,black locks with albinism and deafness syndrome,['BADS'],,,,,,,,,,,,
mondo:0800301,Friedreich ataxia with retained reflexes,['FARR'],,,,,,,,,,,,
mondo:0800302,glycogen storage disease Id,['GSD1D'],,,,,,,,,,,,
mondo:0800304,"neuropathy, hereditary sensory and autonomic, type IId",['HSAN2D'],,,,,,,,,,,,
mondo:0800305,myelofibrosis with myeloid metaplasia,['MMM'],,,,,,,,,,,,
mondo:0800306,"epilepsy, progressive myoclonic, 2b",['EPM2B'],,,,,,,,,,,,
mondo:0800307,de la Chapelle dysplasia,['DLCD'],,,,,,,,,,,,
mondo:0800308,orotic aciduria without megaloblastic anemia,['OAWA'],,,,,,,,,,,,
mondo:0800310,"pregnancy loss, recurrent, 4",['RPRGL4'],,,,,,,,,,,,
mondo:0800311,"vas deferens, congenital unilateral aplasia of",['CUAVD'],,,,,,,,,,,,
mondo:0800312,"wooly hair, autosomal recessive 1, with or without hypotrichosis",['ARWH1'],,,,,,,,,,,,
mondo:0800313,"xeroderma pigmentosum, type F/cockayne syndrome",['XPF/CS'],,,,,,,,,,,,
mondo:0800314,"xeroderma pigmentosum, type G/cockayne syndrome",['XPG/CS'],,,,,,,,,,,,
mondo:0800317,premature ovarian failure 4,['POF4'],,,,,,,,,,,,
mondo:0800318,"Emery-Dreifuss muscular dystrophy 6, X-linked",['EDMD6'],,,,,,,,,,,,
mondo:0800319,"cone dystrophy 5, X-linked",['COD5'],,,,,,,,,,,,
mondo:0800320,"cone dystrophy 1, X-linked",['COD1'],,,,,,,,,,,,
mondo:0800321,"congenital heart defects, multiple types, 1, X-linked",['CHTD1'],,,,,,,,,,,,
mondo:0800322,membranous obstruction of inferior vena cava,['MOVC'],,,,,,,,,,,,
mondo:0800323,long QT syndrome 4,['LQT4'],,,,,,,,,,,,
mondo:0800324,"microphthalmia, isolated, with coloboma 8",['MCOPCB8'],,,,,,,,,,,,
mondo:0800326,cone-rod dystrophy 14,['CORD14'],,,,,,,,,,,,
mondo:0800328,"retinitis pigmentosa 94, variable age at onset",['RP94'],,,,,,,,,,,,
mondo:0800329,"febrile seizures, familial, 3a",['FEB3A'],,,,,,,,,,,,
mondo:0800330,"myoclonic epilepsy, juvenile, 2",['EJM2'],,,,,,,,,,,,
mondo:0800331,"hyperglycinemia, transient neonatal",['TNH'],,,,,,,,,,,,
mondo:0800335,"migraine, familial hemiplegic, 4",['FHM4'],,,,,,,,,,,,
mondo:0800337,acute tubulointerstitial nephritis,['ATIN'],,,,,,,,,,,,
mondo:0800339,"laryngospasm, severe neonatal episodic",['SNEL'],,,,,,,,,,,,
mondo:0800340,"seasonal affective disorder, susceptibility to","['SAD, susceptibility to']",,,,,,,,,,,,
mondo:0800341,"congenital myopathy 4A, autosomal dominant","['CFTD', 'nemaline myopathy 1', 'myopathy, congenital, with fiber-type disproportion', 'fiber-type disproportion myopathy, congenital', 'CFTDM', 'CAPM1', 'NEM1']",,255310,,,,,,,,,,
mondo:0800342,cap myopathy 2,['CAPM2'],,,,,,,,,,,,
mondo:0800344,brachydactyly-syndactyly-oligodactyly syndrome,['BDSDO'],,,,,,,,,,,,
mondo:0800345,"atrial fibrillation, familial, 17",['ATFB17'],,,,,,,,,,,,
mondo:0800346,left ventricular noncompaction 9,['LVNC9'],,,,,,,,,,,,
mondo:0800347,"cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction",['CMH23'],,,,,,,,,,,,
mondo:0800348,retinitis pigmentosa 53,['RP53'],,,,,,,,,,,,
mondo:0800349,"atrial fibrillation, familial, 16",['ATFB16'],,,,,,,,,,,,
mondo:0800350,left ventricular noncompaction 4,['LVNC4'],,,,,,,,,,,,
mondo:0800351,left ventricular noncompaction 5,['LVNC5'],,,,,,,,,,,,
mondo:0800352,retinitis pigmentosa 65,['RP65'],,,,,,,,,,,,
mondo:0800353,"congenital disorder of glycosylation, type Ibb",['CDG1BB'],,,,,,,,,,,,
mondo:0800354,"febrile seizures, familial, 3b",['FEB3B'],,,,,,,,,,,,
mondo:0800355,"parasomnia, sleep terrors type",['PSMNST'],,,,,,,,,,,,
mondo:0800356,"short-rib thoracic dysplasia 7/20 with polydactyly, digenic",['SRTD7/20'],,,,,,,,,,,,
mondo:0800357,"hyperpigmentation, progressive cribriform and zosteriform",['PCZH'],,,,,,,,,,,,
mondo:0800358,schizophrenia 17,['SCZD17'],,,,,,,,,,,,
mondo:0800359,retinitis pigmentosa 64,['RP64'],,,,,,,,,,,,
mondo:0800363,Joubert syndrome 19,['JBTS19'],,,,,,,,,,,,
mondo:0800364,"peroxisome biogenesis disorder, complementation group 3",['CG3'],,,,,,,,,,,,
mondo:0800365,"peroxisome biogenesis disorder, complementation group K",['CGK'],,,,,,,,,,,,
mondo:0800366,"dyskeratosis congenita, autosomal dominant 4",['DKCA4'],0070020,,,,,,,,,,,
mondo:0800367,"cardiomyopathy, dilated, 1LL",['CMD1LL'],,,,,,,,,,,,
mondo:0800368,"cardiomyopathy, dilated, 1MM",['CMD1MM'],0081158,,,,,,,,,,,
mondo:0800369,"parkinson disease 19B, early-onset",['PARK19B'],,,,,,,,,,,,
mondo:0800370,"dyskeratosis congenita, autosomal recessive 7",['DKCB7'],,,,,,,,,,,,
mondo:0800371,"cardiomyopathy, familial restrictive, 5",['RCM5'],,,,,,,,,,,,
mondo:0800372,Joubert syndrome 29,['JBTS29'],0080276,,,,,,,,,,,
mondo:0800373,carbon monoxide poisoning,['CO Poisoning'],,,,,,,,,,,,
mondo:0800374,"ventricular tachycardia, catecholaminergic polymorphic 6",['CPVT6'],,,,,,,,,,,,
mondo:0800375,"developmental delay, epilepsy, and neonatal diabetes 1",['DEND1'],,,,,,,,,,,,
mondo:0800376,"developmental delay, epilepsy, and neonatal diabetes 2",['DEND2'],,,,,,,,,,,,
mondo:0800377,"ACTH-independent adrenal Cushing syndrome, somatic",,,,,,,,,,,,,
mondo:0800378,"17,20-lyase deficiency, isolated",,,,,,,,,,,,,
mondo:0800379,"17-alpha-hydroxylase/17,20-lyase deficiency, combined complete",,,,,,,,,,,,,
mondo:0800380,"17-alpha-hydroxylase/17,20-lyase deficiency, combined partial",,,,,,,,,,,,,
mondo:0800381,"46,XX true hermaphroditism, SRY-positive",,,,,,,,,,,,,
mondo:0800382,Joubert syndrome 11,['JBTS11'],,,,,,,,,,,,
mondo:0800383,Joubert syndrome 34,['JBTS34'],,,,,,,,,,,,
mondo:0800384,cessium poisoning,,,,,,,,,,,,,
mondo:0800385,iron poisoning,"['iron toxicity', 'iron overload']",,,,,,,,,,,,
mondo:0800386,organophosphate poisoning,"['insecticide poisoning', 'organophosphate exposure']",,,,,,,,,,,,
mondo:0800387,sulfur mustard poisoning,"['mustard agent poisoning', 'mustard gas poisoning']",,,,,,,,,,,,
mondo:0800388,cardiac glycoside intoxication,"['cardiac glycoside poisoning', 'digitalis toxicity', 'digitalis intoxication']",,,,,,,,,,,,
mondo:0800389,monochloroacetic acid poisoning,,,,,,,,,,,,,
mondo:0800390,chemotherapy-induced toxicity,,,,,,,,,,,,,
mondo:0800391,EYS-related retinopathy,,,,,,,,,,,,,
mondo:0800392,GNAT2-related retinopathy,,,,,,,,,,,,,
mondo:0800393,IDH3B-related retinopathy,,,,,,,,,,,,,
mondo:0800394,MERTK-related retinopathy,,,,,,,,,,,,,
mondo:0800395,PRPF31-related retinopathy,,,,,,,,,,,,,
mondo:0800396,GPR179-related retinopathy,,,,,,,,,,,,,
mondo:0800397,GRM6-related retinopathy,,,,,,,,,,,,,
mondo:0800398,ADAM9-related retinopathy,,,,,,,,,,,,,
mondo:0800399,RP1-related recessive retinopathy,,,,,,,,,,,,,
mondo:0800400,RP1-related dominant retinopathy,,,,,,,,,,,,,
mondo:0800401,CERKL-related retinopathy,,,,,,,,,,,,,
mondo:0800402,TRPM1-related retinopathy,,,,,,,,,,,,,
mondo:0800403,CNGB1-related retinopathy,,,,,,,,,,,,,
mondo:0800404,PCARE-related retinopathy,,,,,,,,,,,,,
mondo:0800405,CNGA1-related retinopathy,,,,,,,,,,,,,
mondo:0800406,ABCA4-related retinopathy,,,,,,,,,,,,,
mondo:0800407,NYX-related retinopathy,,,,,,,,,,,,,
mondo:0800408,urogenital adysplasia,,,,,,,,,,,,,
mondo:0800409,"ventricular fibrillation during myocardial infarction, susceptibility to",,,,,,,,,,,,,
mondo:0800410,"UV-induced skin damage, susceptibility to",,,,,,,,,,,,,
mondo:0800412,yakut short stature syndrome,,,,,,,,,,,,,
mondo:0800413,"antisocial behavior, susceptibility to",,,,,,,,,,,,,
mondo:0800414,"aplastic anemia, susceptibility to",,,,,,,,,,,,,
mondo:0800415,"asthma, aspirin-induced, susceptibility to",,,,,,,,,,,,,
mondo:0800416,"autism, susceptibility to, 1","['autism susceptibility 1, isolated cases', 'AUTS1']",,,,,,,,,,,,
mondo:0800417,"autism, susceptibility to, 4",['AUTS4'],,,,,,,,,,,,
mondo:0800418,"breast cancer, familial, susceptibility to, 1",,,,,,,,,,,,,
mondo:0800419,"breast cancer, familial, susceptibility to, 2",,,,,,,,,,,,,
mondo:0800420,"breast cancer, familial, susceptibility to, 3",,,,,,,,,,,,,
mondo:0800421,"cardiomyopathy, familial hypertrophic, 4, susceptibility to",,,,,,,,,,,,,
mondo:0800422,"cirrhosis, noncryptogenic, susceptibility to",,,,,,,,,,,,,
mondo:0800423,"colorectal cancer, susceptibility to, 4",['CRCS4'],,,,,,,,,,,,
mondo:0800424,"colorectal cancer, susceptibility to, on chromosome 15",,,,,,,,,,,,,
mondo:0800425,"coronary artery disease, severe, susceptibility to",,,,,,,,,,,,,
mondo:0800426,"dengue fever, susceptibility to",,,,,,,,,,,,,
mondo:0800427,"dengue hemorrhagic fever, susceptibility to",,,,,,,,,,,,,
mondo:0800428,"dengue shock syndrome, susceptibility to",,,,,,,,,,,,,
mondo:0800429,"dyslexia, susceptibility to, 4",['DYX4'],,,,,,,,,,,,
mondo:0800430,"dyslexia, susceptibility to, 7",['DYX7'],,,,,,,,,,,,
mondo:0800431,"efavirenz central nervous system toxicity, susceptibility to",,,,,,,,,,,,,
mondo:0800432,"obesity, susceptibility to",,,,,,,,,,,,,
mondo:0800433,"ovarian cancer, familial, susceptibility to, 1",,,,,,,,,,,,,
mondo:0800434,"ovarian cancer, familial, susceptibility to, 2",,,,,,,,,,,,,
mondo:0800435,"ovarian cancer, familial, susceptibility to, 3",,,,,,,,,,,,,
mondo:0800436,"craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development 1","['cerebro facio thoracic dysplasia', 'pascual-Castroviejo syndrome type 1', 'pascual-Castroviejo syndrome', 'CFSMR1', 'CFSMR', 'cerebrofaciothoracic dysplasia']",0081124,213980,1394,,"['-0.10406', '0.11194', '0.007217', '-0.2085', '-0.1556', '-0.06616', '-0.4783', '0.9346', '-1.041', '0.129', '-0.4036', '-0.4526', '-0.0389', '-0.1202', '0.2524', '-0.2544', '0.505', '-0.1782', '-0.06244', '-0.8877', '-0.1694', '0.6294', '0.3838', '0.00659', '0.6177', '-0.08563', '-0.3093', '-0.0798', '0.5645', '0.2045', '0.255', '-0.8936', '0.01897', '-0.02585', '0.1707', '0.05075', '0.08466', '-0.3743', '0.1862', '-0.252', '0.4487', '-0.591', '-0.3577', '-0.354', '0.08826', '-0.7446', '0.2866', '0.5366', '-0.2035', '-0.9233', '0.3796', '-0.0992', '-0.462', '-0.0334', '-0.6455', '0.003891', '-0.3352', '0.12274', '-0.1371', '0.572', '-0.227', '-0.002216', '-0.4875', '-0.3418', '-0.5337', '-0.01308', '0.2361', '0.657', '-0.4873', '0.322', '-0.3003', '0.3394', '0.1412', '-0.2678', '-0.3167', '0.534', '0.5225', '-0.3857', '0.0355', '-0.03348', '0.378', '0.2373', '0.3364', '0.759', '0.002504', '0.2394', '-0.4717', '0.9707', '0.4902', '0.001917', '-0.1067', '0.3774', '0.5923', '-0.4636', '0.98', '0.3682', '0.2228', '-0.2051', '0.5645', '0.376']",,,C565862,,,,
mondo:0800437,Carey-Fineman-Ziter syndrome 1,"['CFZS1', 'CFZS', 'myopathy, congenital nonprogressive with Moebius and Robin sequences', 'Carey-Fineman-Ziter syndrome 1', 'Moebius sequence, Robin complex, and hypotonia', 'myopathy-Moebius-Robin syndrome', 'myopathy, congenital nonprogressive, with Moebius sequence and Robin sequence', 'congenital nonprogressive myopathy with Moebius and Robin sequences', 'Carey Fineman Ziter syndrome']",0080194,254940,,C1850746,,,,C536102,359.89,,,
mondo:0800438,"developmental delay with short stature, dysmorphic facial features, and sparse hair 1","['DEDSSH1', 'developmental delay-short stature-dysmorphic features-sparse hair syndrome', 'developmental delay with short stature, dysmorphic features, and sparse hair 1', 'Loucks-Innes syndrome', 'developmental delay with short stature, dysmorphic facial features, and sparse hair', 'diphtamide deficiency syndrome']",,616901,459061,C4310801,,,,,,,,
mondo:0800439,syndromic complex neurodevelopmental disorder,,,,,,,,,,,,,
mondo:0800440,HAND1 related congenital heart defect,['HAND1-related congenital heart defect'],,,,,,,,,,,,
mondo:0800441,"NKX2.5-related congenital, conduction and myopathic heart disease","['NKX2-5-related congenital, conduction and myopathic heart disease']",,,,,,,,,,,,
mondo:0800442,MYH-6 related congenital heart defects,['MYH6 related congenital heart defects'],,,,,,,,,,,,
mondo:0800443,DEAF1-associated neurodevelopmental disorder,,,,,,,,,,,,,
mondo:0800448,leukoencephalopathy with vanishing white matter,"['myelinosis centralis diffusa', 'CACH/VWM syndrome', 'CACH/VWM', 'leukoencephalopathy with vanishing white matter', 'vanishing white matter leukodystrophy', 'childhood ataxia with diffuse central nervous system hypomyelination', 'vanishing white matter disease', 'vanishing White matter leukodystrophy', 'CACH', 'ovarioleukodystrophy', 'vanishing White matter leukodystrophy with ovarian failure', 'childhood ataxia with central nervous system hypomyelination/vanishing white matter', 'childhood ataxia with central nervous system hypomyelinization', 'CACH syndrome', 'childhood ataxia with central nervous system hypomyelination', 'leukoencephalopathy with vanishing WHITE matter', 'VWM', 'Cree leukoencephalopathy']",0060868,,135,C1858991,"['-0.01936', '0.576', '-0.5103', '0.057', '0.224', '-0.2988', '-0.386', '0.1482', '-0.345', '0.04123', '-0.4255', '-0.1423', '-0.0613', '-0.6416', '0.804', '0.0851', '0.1148', '-0.327', '-0.02892', '0.10095', '0.2145', '-0.566', '0.267', '-0.7793', '-0.2935', '0.1514', '0.07886', '0.08563', '-0.3926', '-0.05093', '0.293', '0.2568', '0.3152', '0.0954', '-0.01476', '0.0132', '-0.3552', '0.1815', '0.2443', '0.1561', '0.756', '-0.661', '0.506', '-0.1637', '0.04065', '-0.185', '-0.1051', '0.0719', '-0.006683', '-0.364', '0.379', '0.4026', '-0.246', '0.1543', '0.4626', '-0.00974', '0.2585', '0.09314', '-0.3552', '-0.044', '-0.4705', '0.1262', '0.1646', '-0.5654', '-0.3618', '0.3342', '0.9937', '0.567', '-0.2396', '0.6665', '-0.4631', '0.03674', '0.07635', '-0.32', '0.2737', '0.07214', '0.1735', '0.4426', '-0.11456', '-0.6646', '0.04034', '-0.2715', '0.1445', '0.6523', '-0.05463', '0.05865', '0.05276', '0.639', '-0.0866', '0.101', '0.307', '0.276', '-0.462', '0.2761', '0.307', '0.811', '0.556', '-0.3271', '0.133', '0.03265']",C122664,,,,,,
mondo:0810000,choroidal neovascularization,,,,,,,,,D020256,,,,0011506
mondo:0850001,congenital neuronal ceroid lipofuscinosis,,,,168486,,,,,,,,,
mondo:0850007,syndromic lacrimal system disorder,,,,519274,,,,,,,,,
mondo:0850008,anterior segment developmental abnormality with extraocular manifestations,,,,519276,,,,,,,,,
mondo:0850009,syndromic microspherophakia,,,,519294,,,,,,,,,
mondo:0850010,congenital optic disk excavation,,,,519333,,,,,,,,,
mondo:0850013,twin anemia-polycythemia sequence,,,,617294,,,,,,,,,
mondo:0850014,twin-reversed arterial perfusion sequence,,,,617297,,,,,,,,,
mondo:0850015,selective intrauterine growth restriction,,,,617301,,,,,,,,,
mondo:0850030,complete hemimelia,,,,498491,,,,,,,,,
mondo:0850046,amniotic fluid embolism,,,,617304,,,,,,,,,
mondo:0850048,classic eosinophilic pustular folliculitis,,,,617408,,,,,,,,,
mondo:0850049,painful legs and moving toes syndrome,,,,617440,,,,,,,,,
mondo:0850050,congenital aphakia-iris hypoplasia-microphthalmia-microcornea syndrome,,,,617449,,,,,,,,,
mondo:0850053,F12-associated cold autoinflammatory syndrome,,,,617919,,,,,,,,,
mondo:0850054,hemophilia B leyden,,,,617930,,,,,,,,,
mondo:0850058,chronic neurovisceral acid sphingomyelinase deficiency,,,,618891,,,,,,,,,
mondo:0850059,hereditary persistence of fetal hemoglobin-intellectual disability syndrome,,,,619233,,,,,,,,,
mondo:0850064,inherited hematologic cancer-predisposing syndrome,,,,619340,,,,,,,,,
mondo:0850065,neonatal-onset severe multisystemic autoinflammatory disease with increased IL18,,,,619363,,,,,,,,,
mondo:0850066,SAMD9L-associated autoinflammatory syndrome,,,,619367,,,,,,,,,
mondo:0850067,immune deficiency due to impaired neutrophil phagocytosis and migration,,,,619941,,,,,,,,,
mondo:0850068,early-onset autoimmunity-autoinflammation-immunodeficiency syndrome,,,,619948,,,,,,,,,
mondo:0850069,familial hyperinflammatory lymphoproliferative immunodeficiency,,,,619953,,,,,,,,,
mondo:0850070,CADINS disease,,,,619972,,,,,,,,,
mondo:0850071,developmental delay-immunodeficiency-leukoencephalopathy-hypohomocysteinemia syndrome,,,,619979,,,,,,,,,
mondo:0850072,non-syndromic unisutural craniosynostosis,,,,620096,,,,,,,,,
mondo:0850073,non-syndromic unicoronal craniosynostosis,,,,620102,,,,,,,,,
mondo:0850074,non-syndromic unilambdoid craniosynostosis,,,,620113,,,,,,,,,
mondo:0850075,non-syndromic unifrontosphenoidal craniosynostosis,,,,620139,,,,,,,,,
mondo:0850076,non-syndromic unisquamosal craniosynostosis,,,,620146,,,,,,,,,
mondo:0850077,non-syndromic multisutural craniosynostosis,,,,620152,,,,,,,,,
mondo:0850078,non-syndromic non-specific multisutural craniosynostosis,,,,620158,,,,,,,,,
mondo:0850079,non-syndromic bilambdoid craniosynostosis,,,,620178,,,,,,,,,
mondo:0850080,non-syndromic unicoronal and sagittal craniosynostosis,,,,620186,,,,,,,,,
mondo:0850081,non-syndromic metopic and sagittal craniosynostosis,,,,620192,,,,,,,,,
mondo:0850082,non-syndromic bicoronal and metopic craniosynostosis,,,,620198,,,,,,,,,
mondo:0850083,non-syndromic bicoronal and sagittal craniosynostosis,,,,620205,,,,,,,,,
mondo:0850084,non-syndromic pansynostosis,,,,620212,,,,,,,,,
mondo:0850087,primary hypomagnesemia-generalized seizures-intellectual disability-obesity syndrome,,,,620363,,,,,,,,,
mondo:0850088,EGF-related primary hypomagnesemia with intellectual disability,,,,620368,,,,,,,,,
mondo:0850089,Gitelman-like kidney tubulopathy due to mitochondrial DNA mutation,,,,620371,,,,,,,,,
mondo:0850090,fibrosis-neurodegeneration-cerebral angiomatosis syndrome,,,,621758,,,,,,,,,
mondo:0850092,post-cardiac arrest syndrome,,0070306,,,,,,,,,,,
mondo:0850093,absence epilepsy,,0070309,,,,,,,,,,,
mondo:0850094,drug-induced hearing loss,,0070310,,,,,,,,,,,
mondo:0850095,X-linked severe syndromic thoracic aortic aneurysm and dissection,,,,622925,,,,,,,,,
mondo:0850096,SBDS-related severe neonatal spondylometaphyseal dysplasia,,,,622934,,,,,,,,,
mondo:0850097,autoimmune limbic encephalitis,,,,623615,,,,,,,,,
mondo:0850098,oligoasthenoteratozoospermia,,0070311,,,,,,,,,,,
mondo:0850099,MIR140-related spondyloepiphyseal dysplasia,,,,623695,,,,,,,,,
mondo:0850100,body integrity dysphoria,,,,623789,,,,,,,,,
mondo:0850101,spitzoid melanoma,,0070326,,,,,,,,,,,
mondo:0850102,non-specific autoimmune supratentorial encephalitis with characteristic antibodies,,,,624166,,,,,,,,,
mondo:0850103,non-specific autoimmune supratentorial encephalitis without characteristic antibodies,,,,624178,,,,,,,,,
mondo:0850104,paraneoplastic isolated brainstem encephalitis,,,,624190,,,,,,,,,
mondo:0850105,non-specific autoimmune brainstem encephalitis with characteristic antibodies,,,,624199,,,,,,,,,
mondo:0850106,non-specific autoimmune brainstem encephalitis without characteristic antibodies,,,,624216,,,,,,,,,
mondo:0850107,postinfectious cerebellitis,,,,624244,,,,,,,,,
mondo:0850108,non-specific autoimmune cerebellar ataxia with characteristic antibodies,,,,624259,,,,,,,,,
mondo:0850109,non-specific autoimmune cerebellar ataxia without characteristic antibodies,,,,624268,,,,,,,,,
mondo:0850110,melanoma in congenital melanocytic nevus,,0070327,,,,,,,,,,,
mondo:0850112,breast implant-associated anaplastic large cell lymphoma,,0070333,,,,,,,,,,,
mondo:0850115,early-onset obesity-hyperphagia-severe developmental delay syndrome,,,,99704,,,,,,,,,
mondo:0850122,solid adenocarcinoma with mucin production,,0080306,,,,,,,,,,,
mondo:0850123,autonomic nervous system benign neoplasm,,0080321,,,,,,,,,,,
mondo:0850125,malignant adenoma,,0080364,,,,,,,,,,,
mondo:0850126,testicular sex cord-stromal benign neoplasm,,0080371,,,,,,,,,,,
mondo:0850127,epithelioid inflammatory myofibroblastic sarcoma,,0080372,,,,,,,,,,,
mondo:0850128,epididymis disease,,0080373,,,,,,,,,,,
mondo:0850129,gastroesophageal cancer,,0080374,,,,,,,,,,,
mondo:0850130,gastroesophageal adenocarcinoma,,0080375,,,,,,,,,,,
mondo:0850144,germ cell benign neoplasm,,0080601,,,,,,,,,,,
mondo:0850149,nephroma,,0080615,,,,,,,,,,,
mondo:0850150,kidney cortex disease,,0080616,,,,,,,,,,,
mondo:0850151,lymph node carcinoma,,0080618,,,,,,,,,,,
mondo:0850152,auditory system benign neoplasm,,0080619,,,,,,,,,,,
mondo:0850154,tongue carcinoma,,0080641,,,,,,,,,,,
mondo:0850156,B-lymphoblastic leukemia/lymphoma MLL rearranged,,0080644,,,,,,,,,,,
mondo:0850157,B-lymphoblastic leukemia/lymphoma with ETV6-RUNX1,,0080645,,,,,,,,,,,
mondo:0850160,B-lymphoblastic leukemia/lymphoma with IL3-IGH,,0080648,,,,,,,,,,,
mondo:0850161,"B-lymphoblastic leukemia/lymphoma, BCR-ABL1–like",,0080650,,,,,,,,,,,
mondo:0850162,B-lymphoblastic leukemia/lymphoma with IAMP21,,0080651,,,,,,,,,,,
mondo:0850170,spinal muscular atrophy type 0,,0080667,,,,,,,,,,,
mondo:0850196,medulloblastoma WNT activated,,0080702,,,,,,,,,,,
mondo:0850197,medulloblastoma SHH activated,,0080703,,,,,,,,,,,
mondo:0850198,medulloblastoma non-WNT/non-SHH,,0080706,,,,,,,,,,,
mondo:0850199,NK cell deficiency,,0080709,,,,,,,,,,,
mondo:0850200,T cell and NK cell immunodeficiency,,0080710,,,,,,,,,,,
mondo:0850201,hereditary alpha tryptasemia syndrome,,0080714,,,,,,,,,,,
mondo:0850223,Libman-Sacks endocarditis,,0080740,,,,,,,,,,,
mondo:0850225,autoimmune cholangitis,,0080742,,,,,,,,,,,
mondo:0850230,chronic urticaria,,0080747,,,,,,,,,,,
mondo:0850231,erythema nodosum,,0080750,,,,,,,,,,,
mondo:0850257,mucinous pancreas adenocarcinoma,,0080782,,,,,,,,,,,
mondo:0850267,childhood acute megakaryoblastic leukemia,,0080794,,,,,,,,,,,
mondo:0850269,core binding factor acute myeloid leukemia,,0080796,,,,,,,,,,,
mondo:0850271,myeloid leukemia associated with down syndrome,,0080798,,,,,,,,,,,
mondo:0850273,salivary gland mucinous adenocarcinoma,,0080800,,,,,,,,,,,
mondo:0850281,mammary analog secretory carcinoma,,0080808,,,,,,,,,,,
mondo:0850282,chronic asthma,,0080809,,,,,,,,,,,
mondo:0850283,acute asthma,,0080810,,,,,,,,,,,
mondo:0850284,extrinsic asthma,,0080811,,,,,,,,,,,
mondo:0850285,environmental induced asthma,,0080819,,,,,,,,,,,
mondo:0850286,exercise-induced bronchoconstriction,,0080821,,,,,,,,,,,
mondo:0850287,aspirin-induced respiratory disease,,0080822,,,,,,,,,,,
mondo:0850289,human betaherpesvirus 5 infectious disease,['human cytomegalovirus infection'],0080827,,,,,,,,,,,
mondo:0850292,subjective cognitive decline,,0080831,,,,,,,,,,,
mondo:0850295,acquired laryngomalacia,,0080834,,,,,,,,,,,
mondo:0850301,pemphigoid,,0080841,,,,,,,,,,,
mondo:0850302,intracranial meningioma,,0080842,,,,,,,,,,,
mondo:0850303,supratentorial meningioma,,0080843,,,,,,,,,,,
mondo:0850306,latent autoimmune diabetes in adults,,0080846,,,,,,,,,,,
mondo:0850312,anaplastic pleomorphic xanthoastrocytoma,,0080854,,,,,,,,,,,
mondo:0850332,IDH-mutant anaplastic astrocytoma,,0080875,,,,,,,,,,,
mondo:0850333,IDH-wildtype anaplastic astrocytoma,,0080876,,,,,,,,,,,
mondo:0850335,IDH-wildtype glioblastoma,,0080878,,,,,,,,,,,
mondo:0850338,"spinal ependymoma, MYCN-amplified",,0080888,,,,,,,,,,,
mondo:0850339,posterior fossa ependymoma,,0080889,,,,,,,,,,,
mondo:0850340,supratentorial ependymoma,,0080890,,,,,,,,,,,
mondo:0850345,lung pleomorphic carcinoma,,0080899,,,,,,,,,,,
mondo:0850346,oral rhabdomyosarcoma,,0080900,,,,,,,,,,,
mondo:0850347,bladder sarcomatoid transitional cell carcinoma,,0080901,,,,,,,,,,,
mondo:0850348,bladder small cell carcinoma,,0080902,,,,,,,,,,,
mondo:0850349,"astroblastoma, MN1-altered",,0080904,,,,,,,,,,,
mondo:0850353,castration-resistant prostate carcinoma,,0080909,,,,,,,,,,,
mondo:0850368,immunoglobulin heavy-and-light chain,,0080935,,,,,,,,,,,
mondo:0850371,nonobstructive coronary artery disease,,0080938,,,,,,,,,,,
mondo:0850388,"childhood supratentorial embryonal tumor with multilayered rosettes, C19MC-altered",,0080956,,,,,,,,,,,
mondo:0850415,rhabdomyolysis-myalgia syndrome,,0080992,,,,,,,,,,,
mondo:0850416,autoimmune epilepsy,,0080994,,,,,,,,,,,
mondo:0850417,tuberculous encephalopathy,,0080995,,,,,,,,,,,
mondo:0850418,diffuse large B-cell lymphoma activated B-cell type,,0080996,,,,,,,,,,,
mondo:0850419,diffuse large B-cell lymphoma germinal center B-cell type,,0080997,,,,,,,,,,,
mondo:0850420,acute necrotizing pancreatitis,,0080998,,,,,,,,,,,
mondo:0850421,acute hemorrhagic pancreatitis,,0080999,,,,,,,,,,,
mondo:0850426,high-grade B-cell lymphoma double-hit/triple-hit,,0081004,,,,,,,,,,,
mondo:0850445,benign peritoneal solitary fibrous tumor,,0081026,,,,,,,,,,,
mondo:0850449,mixed phenotype acute leukemia with BCR-ABL1,,0081036,,,,,,,,,,,
mondo:0850450,mixed phenotype acute leukemia with MLL rearranged,,0081037,,,,,,,,,,,
mondo:0850451,"mixed phenotype acute leukemia, B/myeloid",,0081038,,,,,,,,,,,
mondo:0850452,"mixed phenotype acute leukemia,T/myeloid",,0081039,,,,,,,,,,,
mondo:0850459,primary cutaneous gamma-delta t-cell lymphoma,,0081050,,,,,,,,,,,
mondo:0850461,neurobehavioral disorder with prenatal alcohol exposure,,0081052,,,,,,,,,,,
mondo:0850468,BN2 diffuse large B-cell lymphoma,,0081064,,,,,,,,,,,
mondo:0850469,EZB diffuse large B-cell lymphoma,,0081065,,,,,,,,,,,
mondo:0850470,MCD diffuse large B-cell lymphoma,,0081066,,,,,,,,,,,
mondo:0850471,N1 diffuse large B-cell lymphoma,,0081067,,,,,,,,,,,
mondo:0850472,ST2 diffuse large B-cell lymphoma,,0081068,,,,,,,,,,,
mondo:0850473,A53 diffuse large B-cell lymphoma,,0081069,,,,,,,,,,,
mondo:0850492,"acute myeloid leukemia, t(8;21)(q22; q22.1)",,0081093,,,,,,,,,,,
mondo:0850495,"acute myeloid leukemia, t(1;22)(p13;q13)",,0081096,,,,,,,,,,,
mondo:0850514,inclusion body myopathy and brain white matter abnormalities,,0081121,619733,,,,,,,,,,
mondo:0850519,tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia,,0081132,,,,,,,,,,,
mondo:0850618,injection anthrax,,0081239,,,,,,,,,,,
mondo:0850812,dendritic cell deficiency,,0111963,,,,,,,,,,,
mondo:0851095,KINSSHIP syndrome,,0112383,619297,,,,,,,,,,
mondo:0851100,malignant olfactory nerve neoplasm,,370,,,,,,,,,,,
mondo:0851102,pulmonary artery disease,,60001,,,,,,,,,,,
mondo:0851103,Bartholin^s gland disease,,60002,,,,,,,,,,,
mondo:0851105,cerebrovascular benign neoplasm,,60007,,,,,,,,,,,
mondo:0858910,dropped head syndrome,,0060034,,,,,,,,,,,
mondo:0858916,pituitary blastoma,,0081244,,,,,,,,,,,
mondo:0858917,cauda equina neuroendocrine tumor,,0081245,,,,,,,,,,,
mondo:0858921,EWSR1-negative small round cell tumor,,0081249,,,,,C165671,,,,,,
mondo:0858926,"developmental delay, hypotrophy, and dysmorphic features without moebius syndrome",,0081264,,,,,,,,,,,
mondo:0858939,"diffuse pediatric-type high-grade glioma, H3-wildtype and IDH-wildtype",,0081277,,,,,,,,,,,
mondo:0858940,infant-type hemispheric glioma,,0081278,,,,,,,,,,,
mondo:0858944,myxoid glioneuronal tumor,,0081285,,,,,,,,,,,
mondo:0858950,traumatic brain injury,,0081292,,,,,,,,,,,
mondo:0858956,diffuse leptomeningeal glioneuronal tumor,,0081302,,,,,,,,,,,
mondo:0858957,multinodular and vacuolating neuronal tumor,,0081303,,,,,,,,,,,
mondo:0858958,high-grade astrocytoma with piloid features,,0081304,,,,,,,,,,,
mondo:0858959,polymorphous low grade neuroepithelial tumor of the young,,0081305,,,,,,,,,,,
mondo:0858960,spindle cell oncocytoma,,0081306,,,,,,,,,,,
mondo:0858966,central nervous system tumor with bcor internal tandem duplication,,0081315,,,,,,,,,,,
mondo:0858967,"primary intracranial sarcoma, DICER1-mutant",,0081316,,,,,,,,,,,
mondo:0858974,breast implant illness,,0081323,,,,,,,,,,,
mondo:0858986,autosomal dominant spastic paraplegia type 80,,,,631068,,,,,,,,,
mondo:0858987,autosomal recessive spastic paraplegia type 82,,,,631073,,,,,,,,,
mondo:0858988,autosomal recessive spastic paraplegia type 83,,,,631076,,,,,,,,,
mondo:0858989,autosomal recessive spastic paraplegia type 84,,,,631079,,,,,,,,,
mondo:0858990,autosomal recessive spastic paraplegia type 85,,,,631082,,,,,,,,,
mondo:0858991,autosomal recessive spastic paraplegia type 86,,,,631085,,,,,,,,,
mondo:0858992,autosomal recessive spastic paraplegia type 87,,,,631088,,,,,,,,,
mondo:0858997,cancer of unknown primary site,,,,631251,,,,,,,,,
mondo:0858998,mesomelic dysplasia-digital anomalies-intellectual disability syndrome,,,,632603,,,,,,,,,
mondo:0858999,KDM3B-related intellectual disability-facial dysmorphism-short stature syndrome,,,,633004,,,,,,,,,
mondo:0859000,SLC12A2-related developmental delay-intellectual disability-sensorineural deafness syndrome,,,,633014,,,,,,,,,
mondo:0859001,CPE-related Prader-Willi-like syndrome,,,,633028,,,,,,,,,
mondo:0859002,intellectual disability-early-onset cataract-microcephaly syndrome,,,,633035,,,,,,,,,
mondo:0859003,PAICS deficiency,,,,633099,,,,,,,,,
mondo:0859004,invasive scopulariopsis infection,,,,633124,,,,,,,,,
mondo:0859005,preaxial digit brachydactyly-webbed fingers,,,,633211,,,,,,,,,
mondo:0859006,proximal femoral focal deficiency,,,,633228,,,,,,,,,
mondo:0859007,mosaic Legius syndrome,,,,634511,,,,,,,,,
mondo:0859008,neurofibromatosis/schwannomatosis,,,,634518,,,,,,,,,
mondo:0859046,"rhabdomyosarcoma, embryonal, 2",,,180295,,,,,,,,,,
mondo:0859050,"Schistosoma mansoni infection, susceptibility/resistance to",,,181460,,,,,,,,,,
mondo:0859080,"intellectual developmental disorder, X-linked, syndromic, with pigmentary mosaicism and coarse facies",,,301066,,,,,,,,,,
mondo:0859081,chromosome Xq13 duplication syndrome,,,301069,,,,,,,,,,
mondo:0859082,"thrombophilia, X-linked, due to factor 8 defect",,,301071,,,,,,,,,,
mondo:0859083,systemic lupus erythematosus 17,,,301080,,,,,,,,,,
mondo:0859085,"neurodevelopmental disorder with gait disturbance, dysmorphic facies, and behavioral abnormalities, X-linked",,,301094,,,,,,,,,,
mondo:0859086,"intellectual developmental disorder, X-linked 110",,,301095,,,,,,,,,,
mondo:0859136,Alzahrani-Kuwahara syndrome,,,619268,,,,,,,,,,
mondo:0859137,"neurodevelopmental disorder with spasticity, cataracts, and cerebellar hypoplasia",,,619286,,,,,,,,,,
mondo:0859139,blepharophimosis-impaired intellectual development syndrome,['SMARCA2-related blepharophimosis-intellectual disability syndrome'],,619293,637013,,,,,,,,,
mondo:0859141,neurodevelopmental disorder with dysmorphic facies and cerebellar hypoplasia,,,619306,,,,,,,,,,
mondo:0859142,Hiatt-Neu-Cooper neurodevelopmental syndrome,,,619311,,,,,,,,,,
mondo:0859143,Radio-Tartaglia syndrome,,,619312,,,,,,,,,,
mondo:0859144,Buratti-Harel syndrome,,,619314,,,,,,,,,,
mondo:0859146,"growth restriction, hypoplastic kidneys, alopecia, and distinctive facies",,,619321,,,,,,,,,,
mondo:0859147,Marbach-Rustad progeroid syndrome,,,619322,,,,,,,,,,
mondo:0859148,neurodevelopmental disorder with seizures and gingival overgrowth,,,619323,,,,,,,,,,
mondo:0859149,hypertriglyceridemia 2,,,619324,,,,,,,,,,
mondo:0859150,BDV syndrome,,,619326,,,,,,,,,,
mondo:0859151,"fibromuscular dysplasia, multifocal",,,619329,,,,,,,,,,
mondo:0859152,neurodevelopmental disorder with cerebellar atrophy and motor dysfunction,,,619333,,,,,,,,,,
mondo:0859154,Bartsocas-Papas syndrome 2,,,619339,,,,,,,,,,
mondo:0859155,"chromosome 1p36 deletion syndrome, proximal",,,619343,,,,,,,,,,
mondo:0859156,"dysostosis multiplex, Ain-Naz type",,,619345,,,,,,,,,,
mondo:0859157,visceral myopathy 2,,,619350,,,,,,,,,,
mondo:0859158,"ataxia, intention tremor, and hypotonia syndrome, childhood-onset",,,619352,,,,,,,,,,
mondo:0859159,"deafness, cataract, impaired intellectual development, and polyneuropathy",,,619354,,,,,,,,,,
mondo:0859160,"Mitochondrial complex IV deficiency, nuclear type 22",,,619355,,,,,,,,,,
mondo:0859161,"onychodystrophy, osteodystrophy, impaired intellectual development, and seizures syndrome",,,619356,,,,,,,,,,
mondo:0859162,neurodevelopmental disorder with infantile epileptic spasms,,,619373,,,,,,,,,,
mondo:0859163,Faundes-Banka syndrome,,,619376,,,,,,,,,,
mondo:0859164,osteootohepatoenteric syndrome,,,619377,,,,,,,,,,
mondo:0859165,"neurodevelopmental disorder with hypotonia, facial dysmorphism, and brain abnormalities",,,619383,,,,,,,,,,
mondo:0859166,"visceral leiomyopathy, African degenerative",,,619400,,,,,,,,,,
mondo:0859167,hypokalemic tubulopathy and deafness,,,619406,,,,,,,,,,
mondo:0859168,"myopathy, myofibrillar, 12, infantile-onset, with cardiomyopathy",,,619424,,,,,,,,,,
mondo:0859169,White-Kernohan syndrome,,,619426,,,,,,,,,,
mondo:0859170,retinal dystrophy and microvillus inclusion disease,,,619446,,,,,,,,,,
mondo:0859171,Luo-Schoch-Yamamoto syndrome,,0070416,619460,,,,,,,,,,
mondo:0859172,"hemolytic disease of fetus and newborn, RH-induced",,,619462,,,,,,,,,,
mondo:0859173,sick sinus syndrome 4,,,619464,,,,,,,,,,
mondo:0859174,"Usmani-Riazuddin syndrome, autosomal dominant",,,619467,,,,,,,,,,
mondo:0859175,nephronophthisis-like nephropathy 2,,,619468,,,,,,,,,,
mondo:0859176,neurodevelopmental disorder with motor and speech delay and behavioral abnormalities,,,619470,,,,,,,,,,
mondo:0859177,VISS syndrome,,,619472,,,,,,,,,,
mondo:0859178,"developmental delay, impaired speech, and behavioral abnormalities",,,619475,,,,,,,,,,
mondo:0859179,neurodevelopmental disorder with dysmorphic facies and thin corpus callosum,,,619480,,,,,,,,,,
mondo:0859180,"bile acid malabsorption, primary, 2",,,619481,,,,,,,,,,
mondo:0859181,DEGCAGS syndrome,,,619488,,,,,,,,,,
mondo:0859182,"Short stature, Dauber-Argente type",,,619489,,,,,,,,,,
mondo:0859183,"Parkinson disease 24, autosomal dominant, susceptibility to",,,619491,,,,,,,,,,
mondo:0859184,ventriculomegaly and arthrogryposis,,,619501,,,,,,,,,,
mondo:0859185,neurodevelopmental disorder with hypotonia and dysmorphic facies,,,619503,,,,,,,,,,
mondo:0859186,Chopra-Amiel-Gordon syndrome,,,619504,,,,,,,,,,
mondo:0859187,neurodevelopmental disorder with hypotonia and brain abnormalities,,,619512,,,,,,,,,,
mondo:0859188,neurodevelopmental disorder with seizures and brain abnormalities,,,619517,,,,,,,,,,
mondo:0859189,"muscular dystrophy, congenital hearing loss, and ovarian insufficiency syndrome",,,619518,,,,,,,,,,
mondo:0859190,neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities,,,619522,,,,,,,,,,
mondo:0859191,"biliary, renal, neurologic, and skeletal syndrome",,,619534,,,,,,,,,,
mondo:0859192,cerebral cavernous malformation 4,['cerebral cavernous malformations 4'],,619538,,,,,,,,,,
mondo:0859193,neuroocular syndrome,,,619539,,,,,,,,,,
mondo:0859194,Boudin-Mortier syndrome,,,619543,,,,,,,,,,
mondo:0859196,"Usmani-Riazuddin syndrome, autosomal recessive",,,619548,,,,,,,,,,
mondo:0859197,"intellectual developmental disorder with hypotonia, impaired speech, and dysmorphic facies",,0081262,619556,,,,,,,,,,
mondo:0859198,"short stature, impaired intellectual development, microcephaly, hypotonia, and ocular anomalies",,,619557,,,,,,,,,,
mondo:0859199,developmental delay with or without intellectual impairment or behavioral abnormalities,,,619575,,,,,,,,,,
mondo:0859200,"cerebellar ataxia, brain abnormalities, and cardiac conduction defects",['neurodevelopmental delay-hypotonia-cerebellar ataxia-cardiac conduction defects syndrome'],,619576,641361,,,,,,,,,
mondo:0859201,neurodevelopmental disorder with impaired language and ataxia and with or without seizures,,,619580,,,,,,,,,,
mondo:0859202,"developmental delay, hypotonia, musculoskeletal defects, and behavioral abnormalities",,,619595,,,,,,,,,,
mondo:0859203,"rhizomelic dysplasia, Ain-Naz type",,,619598,,,,,,,,,,
mondo:0859204,"fetal akinesia, respiratory insufficiency, microcephaly, polymicrogyria, and dysmorphic facies",,,619602,,,,,,,,,,
mondo:0859205,"delayed puberty, self-limited",,,619613,,,,,,,,,,
mondo:0859206,neurodevelopmental disorder with hearing loss and spasticity,,,619616,,,,,,,,,,
mondo:0859207,neurodevelopmental disorder with hypotonia and gross motor and speech delay,,,619639,,,,,,,,,,
mondo:0859208,Hengel-Maroofian-Schols syndrome,,0070408,619641,,,,,,,,,,
mondo:0859209,Zaki syndrome,,,619648,,,,,,,,,,
mondo:0859210,chromosome 16q12 duplication syndrome,,,619649,,,,,,,,,,
mondo:0859211,neurodevelopmental disorder with hyperkinetic movements and dyskinesia,,,619651,,,,,,,,,,
mondo:0859212,"neurodevelopmental disorder, nonprogressive, with spasticity and transient opisthotonus",,,619653,,,,,,,,,,
mondo:0859213,"congenital heart defects, multiple types, 8, with or without heterotaxy",,,619657,,,,,,,,,,
mondo:0859214,Marbach-Schaaf neurodevelopmental syndrome,,,619680,,,,,,,,,,
mondo:0859215,"dystonia, early-onset, and/or spastic paraplegia",,,619681,,,,,,,,,,
mondo:0859216,"neurodevelopmental disorder with microcephaly, seizures, and neonatal cholestasis",,,619685,,,,,,,,,,
mondo:0859217,Brunet-Wagner neurodevelopmental syndrome,,,619690,,,,,,,,,,
mondo:0859218,developmental delay with variable neurologic and brain abnormalities,,,619694,,,,,,,,,,
mondo:0859219,Rauch-Steindl syndrome,,,619695,,,,,,,,,,
mondo:0859220,Ferguson-Bonni neurodevelopmental syndrome,,,619699,,,,,,,,,,
mondo:0859221,Yoon-Bellen neurodevelopmental syndrome,,,619701,,,,,,,,,,
mondo:0859222,"heterotaxy, visceral, 12, autosomal",,,619702,,,,,,,,,,
mondo:0859223,"congenital disorder of glycosylation, type Iw, autosomal dominant",,,619714,,,,,,,,,,
mondo:0859224,intellectual disability and myopathy syndrome,,,619719,,,,,,,,,,
mondo:0859225,neurodevelopmental disorder with or without variable movement or behavioral abnormalities,,,619725,,,,,,,,,,
mondo:0859226,"craniotubular dysplasia, Ikegawa type",,0112340,619727,,,,,,,,,,
mondo:0859228,combined oxidative phosphorylation deficiency 55,,,619743,,,,,,,,,,
mondo:0859229,"cerebellar dysfunction, impaired intellectual development, and hypogonadotropic hypogonadism",,,619761,,,,,,,,,,
mondo:0859230,Kury-Isidor syndrome,,,619762,,,,,,,,,,
mondo:0859231,"macrocephaly, neurodevelopmental delay, lymphoid hyperplasia, and persistent fetal hemoglobin",,,619769,,,,,,,,,,
mondo:0859232,neurodevelopmental disorder with central hypotonia and dysmorphic facies,,,619797,,,,,,,,,,
mondo:0859233,"epidermolysis bullosa, junctional 6, with pyloric atresia",,,619817,,,,,,,,,,
mondo:0859234,"agammaglobulinemia 8b, autosomal recessive",,0081143,619824,,,,,,,,,,
mondo:0859235,"auditory neuropathy, autosomal dominant 3",,0112373,619832,,,,,,,,,,
mondo:0859236,neurodevelopmental disorder with neuromuscular and skeletal abnormalities,,,619833,,,,,,,,,,
mondo:0859237,"3-methylglutaconic aciduria, type VIIA",,0081133,619835,,,,,,,,,,
mondo:0859238,"hypoalphalipoproteinemia, primary, 2, intermediate",,,619836,,,,,,,,,,
mondo:0859239,Chilton-Okur-Chung neurodevelopmental syndrome,,,619841,,,,,,,,,,
mondo:0859240,intellectual developmental disorder with or without peripheral neuropathy,,,619844,,,,,,,,,,
mondo:0859241,"neurodegeneration, childhood-onset, with progressive microcephaly",,,619847,,,,,,,,,,
mondo:0859242,"leukodystrophy, hypomyelinating, 24",,0070406,619851,,,,,,,,,,
mondo:0859243,"neurodevelopmental disorder with hypotonia, impaired speech, and behavioral abnormalities",,,619854,,,,,,,,,,
mondo:0859244,phosphoribosylaminoimidazole carboxylase deficiency,,,619859,,,,,,,,,,
mondo:0859245,"spinocerebellar ataxia, autosomal recessive 32",,0070413,619862,,,,,,,,,,
mondo:0859246,"leukodystrophy, childhood-onset, remitting",,,619864,,,,,,,,,,
mondo:0859247,neurocardiofaciodigital syndrome,,,619869,,,,,,,,,,
mondo:0859248,"corneal dystrophy, punctiform and polychromatic pre-descemet",,,619871,,,,,,,,,,
mondo:0859249,parenti-mignot neurodevelopmental syndrome,,,619873,,,,,,,,,,
mondo:0859250,"neurodevelopmental disorder with microcephaly, hypotonia, nystagmus, and seizures",,,619876,,,,,,,,,,
mondo:0859251,Dentici-Novelli neurodevelopmental syndrome,,,619877,,,,,,,,,,
mondo:0859252,neurodevelopmental disorder with poor growth and skeletal anomalies,,,619880,,,,,,,,,,
mondo:0859253,"osteoporosis, childhood- or juvenile-onset, with developmental delay",,,619884,,,,,,,,,,
mondo:0859254,hepatorenocardiac degenerative fibrosis,,,619902,,,,,,,,,,
mondo:0859255,"peripheral motor neuropathy, childhood-onset, biotin-responsive",,,619903,,,,,,,,,,
mondo:0859256,neurodevelopmental disorder with language delay and seizures,,,619908,,,,,,,,,,
mondo:0859257,intellectual developmental disorder with language impairment and early-onset DOPA-responsive dystonia-parkinsonism,,,619911,,,,,,,,,,
mondo:0859258,neurodevelopmental disorder with dystonia and seizures,,,619922,,,,,,,,,,
mondo:0859260,Dworschak-Punetha neurodevelopmental syndrome,,,619955,,,,,,,,,,
mondo:0859261,attention deficit-hyperactivity disorder 8,,,619957,,,,,,,,,,
mondo:0859262,ACCES syndrome,['aplasia cutis congenita with ectrodactyly skeletal syndrome'],,619959,,,,,,,,,,
mondo:0859263,"developmental delay, impaired speech, and behavioral abnormalities, with or without seizures",,,619964,,,,,,,,,,
mondo:0859264,congenital myopathy 11,,,619967,,,,,,,,,,
mondo:0859265,neurodevelopmental disorder with epilepsy and brain atrophy,,,619971,,,,,,,,,,
mondo:0859266,"neurodevelopmental disorder with severe motor impairment, absent language, cerebral hypomyelination, and brain atrophy",,,619972,,,,,,,,,,
mondo:0859267,tumor predisposition syndrome 2,,,619975,,,,,,,,,,
mondo:0859271,glycosylphosphatidylinositol biosynthesis defect 25,,,619985,,,,,,,,,,
mondo:0859272,neurodevelopmental disorder with speech delay and variable ocular anomalies,,,619989,,,,,,,,,,
mondo:0859273,"liver disease, severe congenital",,,619991,,,,,,,,,,
mondo:0859274,"neurodevelopmental disorder with intention tremor, pyramidal signs, dyspraxia, and ocular anomalies",,,619995,,,,,,,,,,
mondo:0859275,"neurodevelopmental disorder with spasticity, seizures, and brain abnormalities",,,620001,,,,,,,,,,
mondo:0859276,primordial dwarfism-immunodeficiency-lipodystrophy syndrome,,,620005,,,,,,,,,,
mondo:0859277,intellectual developmental disorder with muscle tone abnormalities and distal skeletal defects,,,620007,,,,,,,,,,
mondo:0859278,"keratoderma-ichthyosis-deafness syndrome, autosomal recessive",,,620009,,,,,,,,,,
mondo:0859279,"spinal muscular atrophy, distal, autosomal recessive, 6",['DSMA6'],,620011,,,,,,,,,,
mondo:0859280,"developmental delay, hypotonia, and impaired language",,0070420,620012,,,,,,,,,,
mondo:0859281,intellectual developmental disorder with autism and dysmorphic facies,,,620021,,,,,,,,,,
mondo:0859282,"neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures",,,620023,,,,,,,,,,
mondo:0859283,"neurodevelopmental disorder with seizures, microcephaly, and brain abnormalities",,,620024,,,,,,,,,,
mondo:0859285,"neurodevelopmental disorder with microcephaly, short stature, and speech delay",,,620027,,,,,,,,,,
mondo:0859286,"neurodevelopmental disorder with hypotonia, language delay, and skeletal defects with or without seizures",,,620029,,,,,,,,,,
mondo:0859287,"neurodevelopmental disorder with microcephaly, hypotonia, and absent language",,,620038,,,,,,,,,,
mondo:0859288,bone marrow failure and diabetes mellitus syndrome,,,620044,,,,,,,,,,
mondo:0859289,intestinal dysmotility syndrome,,,620045,,,,,,,,,,
mondo:0859290,familial apolipoprotein gene cluster deletion syndrome,,,620058,,,,,,,,,,
mondo:0859292,"developmental delay, behavioral abnormalities, and neuropsychiatric disorders",,,620065,,,,,,,,,,
mondo:0859293,"neurodevelopmental disorder with microcephaly, cerebral atrophy, and visual impairment",,,620066,,,,,,,,,,
mondo:0859295,"neurodevelopmental disorder with short stature, prominent forehead, and feeding difficulties",,,620070,,,,,,,,,,
mondo:0859296,"neurodevelopmental disorder with poor growth, spastic tetraplegia, and hearing loss",,0081324,620071,,,,,,,,,,
mondo:0859297,neurodevelopmental disorder with dysmorphic facies and skeletal and brain abnormalities,,,620073,,,,,,,,,,
mondo:0859298,"neurodevelopmental disorder with facial dysmorphism, absent language, and pseudo-pelger-huet anomaly",,,620075,,,,,,,,,,
mondo:0859300,"Neuronopathy, distal hereditary motor, type X",,,620080,,,,,,,,,,
mondo:0859301,neurodevelopmental disorder with craniofacial dysmorphism and skeletal defects,,,620083,,,,,,,,,,
mondo:0859302,hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 2,,,620085,,,,,,,,,,
mondo:0859303,intellectual developmental disorder with ocular anomalies and distinctive facial features,,0081301,620086,,,,,,,,,,
mondo:0859304,"neurodegeneration, childhood-onset, with multisystem involvement due to mitochondrial dysfunction",,,620089,,,,,,,,,,
mondo:0859305,neurodevelopmental disorder with eye movement abnormalities and ataxia,,0081275,620094,,,,,,,,,,
mondo:0859306,developmental delay with variable intellectual disability and dysmorphic facies,,,620098,,,,,,,,,,
mondo:0859307,cleidocranial dysplasia 2,,,620099,,,,,,,,,,
mondo:0859308,retinitis pigmentosa 95,,,620102,,,,,,,,,,
mondo:0859309,"spastic paraplegia 88, autosomal dominant",,,620106,,,,,,,,,,
mondo:0859310,orofaciodigital syndrome 19,,,620107,,,,,,,,,,
mondo:0859311,"Charcot-Marie-Tooth disease, demyelinating, type 1J",,,620111,,,,,,,,,,
mondo:0859312,"neurodevelopmental disorder with growth retardation, dysmorphic facies, and corpus callosum abnormalities",,,620113,,,,,,,,,,
mondo:0859313,neurodevelopmental disorder with speech impairment and with or without seizures,,,620114,,,,,,,,,,
mondo:0859314,developmental and epileptic encephalopathy 108,,0070394,620115,,,,,,,,,,
mondo:0859316,"iron overload, susceptibility to",,,620121,,,,,,,,,,
mondo:0859317,"pseudohypoaldosteronism, type IB2, autosomal recessive",,,620125,,,,,,,,,,
mondo:0859318,"pseudohypoaldosteronism, type IB3, autosomal recessive",,,620126,,,,,,,,,,
mondo:0859319,"dyskeratosis congenita, autosomal recessive 8",,,620133,,,,,,,,,,
mondo:0859320,"mitochondrial complex I deficiency, nuclear type 39",,,620135,,,,,,,,,,
mondo:0859321,"mitochondrial complex 3 deficiency, nuclear type 11",,,620137,,,,,,,,,,
mondo:0859322,"myopathy with myalgia, increased serum creatine kinase, and with or without episodic rhabdomyolysis",,,620138,,,,,,,,,,
mondo:0859323,combined oxidative phosphorylation deficiency 56,,,620139,,,,,,,,,,
mondo:0859324,"developmental delay, language impairment, and ocular abnormalities",,,620141,,,,,,,,,,
mondo:0859325,developmental and epileptic encephalopathy 109,,0070378,620145,,,,,,,,,,
mondo:0859327,developmental and epileptic encephalopathy 110,,0070395,620149,,,,,,,,,,
mondo:0859328,"hypomagnesemia 7, renal, with or without dilated cardiomyopathy",,,620152,,,,,,,,,,
mondo:0859329,mosaic variegated aneuploidy syndrome 4,,,620153,,,,,,,,,,
mondo:0859330,oocyte maturation defect 13,,,620154,,,,,,,,,,
mondo:0859331,Rabin-Pappas syndrome,,,620155,,,,,,,,,,
mondo:0859332,"cortical dysplasia, complex, with other brain malformations 11",,,620156,,,,,,,,,,
mondo:0859333,"intellectual developmental disorder, autosomal dominant 70",,,620157,,,,,,,,,,
mondo:0859334,spinocerebellar ataxia 50,,,620158,,,,,,,,,,
mondo:0859335,congenital myopathy 15,,0081347,620161,,,,,,,,,,
mondo:0859336,"muscular dystrophy, congenital, with or without seizures",,,620166,,,,,,,,,,
mondo:0859337,combined oxidative phosphorylation deficiency 57,,,620167,,,,,,,,,,
mondo:0859338,spermatogenic failure 78,,,620170,,,,,,,,,,
mondo:0859339,"tooth agenesis, selective, 10",,,620173,,,,,,,,,,
mondo:0859340,"spinocerebellar ataxia 27B, late-onset",,,620174,,,,,,,,,,
mondo:0859341,hypotrichosis 15,,,620177,,,,,,,,,,
mondo:0859342,"microcephaly 30, primary, autosomal recessive",,,620183,,,,,,,,,,
mondo:0859345,"branchial arch abnormalities, choanal atresia, athelia, hearing loss, and hypothyroidism syndrome",,,620186,,,,,,,,,,
mondo:0859346,mosaic variegated aneuploidy syndrome 7 with inflammation and tumor predisposition,,,620189,,,,,,,,,,
mondo:0859347,"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skin abnormalities",,,620191,,,,,,,,,,
mondo:0859350,"neurodevelopmental disorder with poor growth, large ears, and dysmorphic facies",,,620194,,,,,,,,,,
mondo:0859351,obesity and hypopigmentation,,,620195,,,,,,,,,,
mondo:0859352,spermatogenic failure 79,,,620196,,,,,,,,,,
mondo:0859353,"ciliary dyskinesia, primary, 49, without situs inversus",,,620197,,,,,,,,,,
mondo:0859354,"thyroid hormone metabolism, abnormal, 3",,,620198,,,,,,,,,,
mondo:0859355,inflammatory poikiloderma with hair abnormalities and acral keratoses,,,620199,,,,,,,,,,
mondo:0859356,"congenital disorder of glycosylation, type IIy",,,620200,,,,,,,,,,
mondo:0859357,"congenital disorder of glycosylation, type IIz",,,620201,,,,,,,,,,
mondo:0859358,"cardiomyopathy, dilated, 2H",,,620203,,,,,,,,,,
mondo:0859360,"spinocerebellar ataxia, autosomal recessive 33",,0070414,620208,,,,,,,,,,
mondo:0859361,neurodevelopmental disorder with dysmorphic facies and ischiopubic hypoplasia,,,620210,,,,,,,,,,
mondo:0859362,"hyperinsulinemic hypoglycemia, familial, 8",,0081328,620211,,,,,,,,,,
mondo:0859363,"spastic paraplegia 79A, autosomal dominant, with ataxia",,,620221,,,,,,,,,,
mondo:0859364,spermatogenic failure 80,,,620222,,,,,,,,,,
mondo:0859365,"neurodevelopmental disorder with hypotonia, dysmorphic facies, and skeletal anomalies, with or without seizures",,,620224,,,,,,,,,,
mondo:0859366,"hearing loss, autosomal dominant 85","['deafness, autosomal dominant 85']",,620227,,,,,,,,,,
mondo:0859367,retinitis pigmentosa 96,,,620228,,,,,,,,,,
mondo:0859368,short QT syndrome 7,,,620231,,,,,,,,,,
mondo:0859369,"joint contractures, osteochondromas, and B-cell lymphoma",,,620232,,,,,,,,,,
mondo:0859370,"respiratory infections, recurrent, and failure to thrive with or without diarrhea",,,620233,,,,,,,,,,
mondo:0859371,"rhabdomyolysis, susceptibility to, 1",,,620235,,,,,,,,,,
mondo:0859372,"cardiomyopathy, familial hypertrophic, 29, with polyglucosan bodies",,,620236,,,,,,,,,,
mondo:0859373,"intellectual developmental disorder, autosomal recessive 78",,,620237,,,,,,,,,,
mondo:0859374,"hearing loss, autosomal recessive 120","['deafness, autosomal recessive 120']",,620238,,,,,,,,,,
mondo:0859375,"developmental delay with hypotonia, myopathy, and brain abnormalities",,,620240,,,,,,,,,,
mondo:0859376,"hydrocephalus, congenital, 5, susceptibility to",,,620241,,,,,,,,,,
mondo:0859377,neurodevelopmental disorder with poor growth and behavioral abnormalities,,,620242,,,,,,,,,,
mondo:0859378,"leukodystrophy, hypomyelinating, 25",,0070401,620243,,,,,,,,,,
mondo:0859379,lymphatic malformation 13,,,620244,,,,,,,,,,
mondo:0859380,episodic kinesigenic dyskinesia 3,,,620245,,,,,,,,,,
mondo:0859381,"cardiomyopathy, dilated, 100",,,620247,,,,,,,,,,
mondo:0859382,cataract 50 with or without glaucoma,,,620253,,,,,,,,,,
mondo:0859383,ichthyosis hystrix,,,,,,,,,,,,,
mondo:0859390,"epilepsy, X-linked, with or without impaired intellectual development and dysmorphic features",,,,,,,,,,,,,
mondo:0859393,Atelis syndrome,,,,,,,,,,,,,
mondo:0859477,"spermatogenic failure, X-linked, 5",,,301099,,,,,,,,,,
mondo:0859478,"spermatogenic failure, X-linked, 6",,,301101,,,,,,,,,,
mondo:0859514,congenital myopathy 18,,0081350,620246,,,,,,,,,,
mondo:0859515,"congenital myopathy 10b, mild variant",,0081345,620249,,,,,,,,,,
mondo:0859516,"neurodevelopmental disorder with seizures, spasticity, and complete or partial agenesis of the corpus callosum",,,620250,,,,,,,,,,
mondo:0859517,"congenital myopathy 2b, severe infantile, autosomal recessive",,0081339,620265,,,,,,,,,,
mondo:0859518,"leukodystrophy, hypomyelinating, 26, with chondrodysplasia",,0070403,620269,,,,,,,,,,
mondo:0859519,neurodevelopmental disorder with absent speech and movement and behavioral abnormalities,,,620270,,,,,,,,,,
mondo:0859520,"Mitochondrial complex IV deficiency, nuclear type 23",,,620275,,,,,,,,,,
mondo:0859521,oocyte maturation defect 14,,,620276,,,,,,,,,,
mondo:0859522,spermatogenic failure 81,,,620277,,,,,,,,,,
mondo:0859523,"congenital myopathy 2c, severe infantile, autosomal dominant",,0081340,620278,,,,,,,,,,
mondo:0859524,"hearing loss, autosomal dominant 86",,,620280,,,,,,,,,,
mondo:0859525,"hearing loss, autosomal dominant 87",,,620281,,,,,,,,,,
mondo:0859526,immunodeficiency 109 with lymphoproliferation,,,620282,,,,,,,,,,
mondo:0859527,"hearing loss, autosomal dominant 88",,,620283,,,,,,,,,,
mondo:0859528,"hearing loss, autosomal dominant 89",,,620284,,,,,,,,,,
mondo:0859529,"amyotrophic lateral sclerosis 27, juvenile",,,620285,,,,,,,,,,
mondo:0859530,"myopathy, sarcoplasmic body",,,620286,,,,,,,,,,
mondo:0859531,"neurodevelopmental disorder with language delay and behavioral abnormalities, with or without seizures",,,620292,,,,,,,,,,
mondo:0859532,"congenital heart defects, multiple types, 9",,,620294,,,,,,,,,,
mondo:0859564,"epilepsy, X-linked 2, with or without impaired intellectual development and dysmorphic features",,,301091,,,,,,,,,,
mondo:0859565,atrioventricular septal defect,,,606215,,,,,,,,,,
mondo:0859567,"craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2",,0081125,616994,,,,,,,,,,
mondo:0859568,"macular dystrophy, retinal, 4",,,619977,,,,,,,,,,
mondo:0859569,braddock-carey syndrome 1,,,619980,,,,,,,,,,
mondo:0859570,braddock-carey syndrome 2,,,619981,,,,,,,,,,
mondo:0859571,"diaphragmatic hernia 4, with cardiovascular defects",,,620025,,,,,,,,,,
mondo:0859572,cardiac valvular dysplasia 2,,,620067,,,,,,,,,,
mondo:0859573,bent bone dysplasia syndrome 2,,,620076,,,,,,,,,,
mondo:0859574,"ichthyosis, annular epidermolytic, 2",,,620148,,,,,,,,,,
mondo:0859575,Atelis syndrome 1,,,620184,,,,,,,,,,
mondo:0859576,Atelis syndrome 2,,,620185,,,,,,,,,,
mondo:0859577,lacrimoauriculodentodigital syndrome 2,,,620192,,,,,,,,,,
mondo:0859578,lacrimoauriculodentodigital syndrome 3,,,620193,,,,,,,,,,
mondo:0859588,keratosis pilaris atrophicans faciei,,0080752,,,,,,,,,,,
mondo:0859591,childhood low-grade glioma,,0080830,,,,,,,,,,,
mondo:0859592,IDH-mutant and 1p/19q-codeleted oligodendroglioma,,0080882,,,,,,,,,,,
mondo:0859597,cns neuroblastoma with FOXR2 activation,,0080906,,,,,,,,,,,
mondo:0859598,erythroleukemia,,0080916,,,,,,,,,,,
mondo:0859614,"diffuse low-grade glioma, MAPK pathway–altered",,0081260,,,,,,,,,,,
mondo:0859615,"diffuse astrocytoma, MYB- or MYBL1-altered",,0081279,,,,,,,,,,,
mondo:0859689,hepatobiliary benign neoplasm,,3117,,,,,,,,,,,
mondo:0859690,malignant cystadenoma,,60004,,,,,,,,,,,
mondo:0859692,immune-mediated cerebellar ataxia,,,,623638,,,,,,,,,
mondo:0859747,grade I lymphomatoid granulomatosis,,0081308,,,,,,,,,,,
mondo:0859748,grade II lymphomatoid granulomatosis,,0081309,,,,,,,,,,,
mondo:0859749,grade III lymphomatoid granulomatosis,,0081310,,,,,,,,,,,
mondo:0859761,SLC12A2-related autosomal recessive neonatal-developmental delay-intellectual disability-feeding difficulty-sensorineural deafness syndrome,,,,633021,,,,,,,,,
mondo:0859762,SLC12A2-related autosomal dominant infantile-developmental delay-intellectual disability-sensorineural deafness syndrome,,,,633024,,,,,,,,,
mondo:0859763,mosaic neurofibromatosis type 1,,,,634461,,,,,,,,,
mondo:0859764,mosaic NF2-related schwannomatosis,,,,634475,,,,,,,,,
mondo:0859765,mosaic schwannomatosis,,,,634492,,,,,,,,,
mondo:0957001,hereditary mixed dermis disorder,,,,183481,,,,,,,,,
mondo:0957003,hereditary neuro-ophthalmological disease,['genetic neuro-ophthalmological disease'],,,183616,,,,,,,,,
mondo:0957008,hereditary cerebral malformation,['genetic cerebral malformation'],,,269553,,,,,,,,,
mondo:0957009,hereditary posterior fossa malformation,['genetic posterior fossa malformation'],,,269557,,,,,,,,,
mondo:0957018,autoinflammatory syndrome of childhood,,,,319719,,,,,,,,,
mondo:0957024,"hereditary 46,XX disorder of sex development","['genetic 46,XX disorder of sex development']",,,325697,,,,,,,,,
mondo:0957025,"hereditary 46,XY disorder of sex development","['genetic 46,XY disorder of sex development']",,,325706,,,,,,,,,
mondo:0957048,isolated macular dystrophy,,,,519302,,,,,,,,,
mondo:0957097,hereditary hemolytic uremic syndrome,['genetic hemolytic uremic syndrome'],,,576742,,,,,,,,,
mondo:0957111,neurological muscular channelopathy due to a genetic sodium channel defect,,,,98738,,,,,,,,,
mondo:0957112,neurological muscular channelopathy due to a genetic chloride channel defect,,,,98739,,,,,,,,,
mondo:0957113,neurological muscular channelopathy due to a genetic calcium channel defect,,,,98740,,,,,,,,,
mondo:0957114,neurological muscular channelopathy due to a genetic potassium channel defect,,,,98741,,,,,,,,,
mondo:0957115,neurological muscular channelopathy due to a genetic ryanodine receptor defect,,,,98742,,,,,,,,,
mondo:0957202,"spermatogenic failure, X-linked, 7",,,301106,,,,,,,,,,
mondo:0957203,"intellectual developmental disorder, X-linked 111",,,301107,,,,,,,,,,
mondo:0957204,autoinflammation with pulmonary and cutaneous vasculitis,,,620296,,,,,,,,,,
mondo:0957208,"pituitary hormone deficiency, combined or isolated, 8",,,620303,,,,,,,,,,
mondo:0957210,neurooculorenal syndrome,,,620305,,,,,,,,,,
mondo:0957211,neurodegeneration and seizures due to copper transport defect,,,620306,,,,,,,,,,
mondo:0957215,congenital myopathy 20,,,620310,,,,,,,,,,
mondo:0957216,premature ovarian failure 21,,,620311,,,,,,,,,,
mondo:0957217,"cortical dysplasia, complex, with other brain malformations 12",,,620316,,,,,,,,,,
mondo:0957218,"neurodevelopmental disorder with microcephaly and speech delay, with or without brain abnormalities",,,620317,,,,,,,,,,
mondo:0957220,oocyte/zygote/embryo maturation arrest 17,,,620319,,,,,,,,,,
mondo:0957221,"spastic paraplegia 70, autosomal recessive",,,620323,,,,,,,,,,
mondo:0957224,congenital myopathy 21 with early respiratory failure,,,620326,,,,,,,,,,
mondo:0957225,"neurodegeneration with developmental delay, early respiratory failure, myoclonic seizures, and brain abnormalities",,,620327,,,,,,,,,,
mondo:0957228,"intellectual developmental disorder, autosomal dominant 71, with behavioral abnormalities",,,620330,,,,,,,,,,
mondo:0957229,hatipoglu immunodeficiency syndrome,,,620331,,,,,,,,,,
mondo:0957230,oocyte/zygote/embryo maturation arrest 18,,,620332,,,,,,,,,,
mondo:0957231,oocyte/zygote/embryo maturation arrest 19,,,620333,,,,,,,,,,
mondo:0957240,cone-rod dystrophy 24,,,620342,,,,,,,,,,
mondo:0957247,"congenital myopathy 22A, classic",,,620351,,,,,,,,,,
mondo:0957248,developmental and epileptic encephalopathy 31B,,,620352,,,,,,,,,,
mondo:0957249,spermatogenic failure 82,,,620353,,,,,,,,,,
mondo:0957250,spermatogenic failure 83,,,620354,,,,,,,,,,
mondo:0957252,"ciliary dyskinesia, primary, 50",,,620356,,,,,,,,,,
mondo:0957253,diarrhea 13,,,620357,,,,,,,,,,
mondo:0957254,"mitochondrial complex V (ATP synthase) deficiency, nuclear type 4A",,,620358,,,,,,,,,,
mondo:0957255,"mitochondrial complex V (ATP synthase) deficiency, nuclear type 7",,,620359,,,,,,,,,,
mondo:0957260,combined low LDL and fibrinogen,,,620364,,,,,,,,,,
mondo:0957261,"pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 7",,,620365,,,,,,,,,,
mondo:0957262,"osteopetrosis, autosomal recessive 9",,,620366,,,,,,,,,,
mondo:0957263,"pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 8",,,620367,,,,,,,,,,
mondo:0957264,cerebroretinal microangiopathy with calcifications and cysts 3,,,620368,,,,,,,,,,
mondo:0957265,"congenital myopathy 22B, severe fetal",,,620369,,,,,,,,,,
mondo:0957266,RECON progeroid syndrome,,,620370,,,,,,,,,,
mondo:0957267,"neurodevelopmental disorder with intracranial hemorrhage, seizures, and spasticity",,,620371,,,,,,,,,,
mondo:0957268,hypersulfaturia,,,620372,,,,,,,,,,
mondo:0957270,"muscular dystrophy, limb-girdle, autosomal recessive 28",,,620375,,,,,,,,,,
mondo:0957271,"autoinflammatory disease, systemic, with vasculitis",,,620376,,,,,,,,,,
mondo:0957273,"Charcot-Marie-Tooth disease, dominant intermediate A",,,620378,,,,,,,,,,
mondo:0957274,"spastic paraplegia 89, autosomal recessive",,,620379,,,,,,,,,,
mondo:0957278,oocyte/zygote/embryo maturation arrest 20,,,620383,,,,,,,,,,
mondo:0957279,"auditory neuropathy, autosomal dominant 2",,,620384,,,,,,,,,,
mondo:0957281,"nemaline myopathy 5B, autosomal recessive, childhood-onset",,,620386,,,,,,,,,,
mondo:0957284,"nemaline myopathy 5C, autosomal dominant",,,620389,,,,,,,,,,
mondo:0957288,"intellectual developmental disorder, autosomal recessive 79",,,620393,,,,,,,,,,
mondo:0957294,"pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9",,,620400,,,,,,,,,,
mondo:0957301,spermatogenic failure 84,,,620409,,,,,,,,,,
mondo:0957303,"palmoplantar keratoderma, epidermolytic, 2",,,620411,,,,,,,,,,
mondo:0957307,woolly hair-skin fragility syndrome,,,620415,,,,,,,,,,
mondo:0957308,"spastic paraplegia 90A, autosomal dominant",,,620416,,,,,,,,,,
mondo:0957309,"spastic paraplegia 90B, autosomal recessive",,,620417,,,,,,,,,,
mondo:0957314,retinitis pigmentosa 97,,,620422,,,,,,,,,,
mondo:0957337,isolated chorioretinal dystrophy,,,,519300,,,,,,,,,
mondo:0957341,secondary early-onset glaucoma,,,,519331,,,,,,,,,
mondo:0957382,multiple mitochondrial dysfunctions syndrome 7,,,620423,,,,,,,,,,
mondo:0957385,"dystonia 37, early-onset, with striatal lesions",,,620427,,,,,,,,,,
mondo:0957386,"neurodevelopmental disorder with motor and language delay, ocular defects, and brain abnormalities",,,620428,,,,,,,,,,
mondo:0957388,"autoimmune disease, multisystem, infantile-onset, 3",,,620430,,,,,,,,,,
mondo:0957396,"ciliary dyskinesia, primary, 51",,,620438,,,,,,,,,,
mondo:0957397,"intellectual developmental disorder, autosomal dominant 72",,,620439,,,,,,,,,,
mondo:0957403,periodic fever syndrome of childhood,,,,324939,,,,,,,,,
mondo:0957404,pyogenic autoinflammatory syndrome of childhood,,,,324942,,,,,,,,,
mondo:0957405,granulomatous autoinflammatory syndrome of childhood,,,,324950,,,,,,,,,
mondo:0957408,type 1 interferonopathy of childhood,,,,481671,,,,,,,,,
mondo:0957421,borna virus encephalitis,,,,637051,,,,,,,,,
mondo:0957423,immunotherapy induced hypophysitis,,,,641350,,,,,,,,,
mondo:0957426,autosomal recessive hyper-IgE syndrome,,,,641368,,,,,,,,,
mondo:0957427,B-lymphoblastic leukemia/lymphoma with t(7;9)(q11.2;p13.2),,,,641372,,,,,,,,,
mondo:0957428,B-lymphoblastic leukemia/lymphoma with t(17;19),,,,641375,,,,,,,,,
mondo:0957430,childhood-onset schizophrenia,,,,641496,,,,,,,,,
mondo:0957431,endogenous Cushing syndrome,,,,641613,,,,,,,,,
mondo:0957432,neonatal compartment syndrome,,,,641829,,,,,,,,,
mondo:0957433,primary pulmonary vein stenosis,,,,642071,,,,,,,,,
mondo:0957442,autosomal recessive ataxia due to PEX16 deficiency,,,,642954,,,,,,,,,
mondo:0957443,autosomal recessive ataxia due to PEX2 deficiency,,,,642965,,,,,,,,,
mondo:0957451,non-terminal myelocystocele,,,,645340,,,,,,,,,
mondo:0957452,segmental arterial mediolysis,,,,645350,,,,,,,,,
mondo:0957453,true myelomeningocele,,,,645383,,,,,,,,,
mondo:0957454,hemi-myelomeningocele,,,,645388,,,,,,,,,
mondo:0957456,classical dermatomyositis,,,,645613,,,,,,,,,
mondo:0957458,adermatopathic dermatomyositis,,,,645626,,,,,,,,,
mondo:0957459,congenital esophageal stenosis,,,,645749,,,,,,,,,
mondo:0957460,spontaneous intestinal perforation,,,,645793,,,,,,,,,
mondo:0957461,primary tuberculous lymphadenitis,,,,645807,,,,,,,,,
mondo:0957462,primary pulmonary tuberculosis,,,,645814,,,,,,,,,
mondo:0957463,primary bone and joint tuberculosis,,,,645822,,,,,,,,,
mondo:0957464,primary cutaneous tuberculosis,,,,645849,,,,,,,,,
mondo:0957465,multifocal tuberculosis,,,,645854,,,,,,,,,
mondo:0957466,primary tuberculosis of the digestive system,,,,645859,,,,,,,,,
mondo:0957467,primary genito-urinary tuberculosis,,,,645874,,,,,,,,,
mondo:0957473,craniosynostosis-facial dysmorphism-chiari-1 malformation-developmental and language delay syndrome,,,,647681,,,,,,,,,
mondo:0957476,isolated persistent urogenital sinus,,,,647794,,,,,,,,,
mondo:0957477,MYT1L-related developmental delay-intellectual disability-obesity syndrome,,,,647799,,,,,,,,,
mondo:0957481,idiopathic pregnancy-associated osteoporosis,,,,647823,,,,,,,,,
mondo:0957487,idiopathic catatonia,,,,648919,,,,,,,,,
mondo:0957494,"autoinflammatory disease, multisystem, with immune dysregulation, X-linked",,,301109,,,,,,,,,,
mondo:0957495,"hemolytic uremic syndrome, atypical, 8, with rhizomelic short stature",,,301110,,,,,,,,,,
mondo:0957496,"intellectual developmental disorder, X-linked 112",,,301111,,,,,,,,,,
mondo:0957497,disabling pansclerotic morphea of childhood,,,620443,,,,,,,,,,
mondo:0957530,"breast-ovarian cancer, familial, susceptibility to, 5",,,620442,,,,,,,,,,
mondo:0957531,neurodevelopmental disorder with microcephaly and movement abnormalities,,,620445,,,,,,,,,,
mondo:0957533,megalencephalic leukoencephalopathy with subcortical cysts 3,,,620447,,,,,,,,,,
mondo:0957534,"megalencephalic leukoencephalopathy with subcortical cysts 4, remitting",,,620448,,,,,,,,,,
mondo:0957535,immunodeficiency 112,,,620449,,,,,,,,,,
mondo:0957536,"intellectual developmental disorder, autosomal dominant 73",,,620450,,,,,,,,,,
mondo:0957537,combined oxidative phosphorylation deficiency 58,,,620451,,,,,,,,,,
mondo:0957538,amyotrophic lateral sclerosis 28,,,620452,,,,,,,,,,
mondo:0957539,"dystonia 22, juvenile-onset",,,620453,,,,,,,,,,
mondo:0957540,"congenital disorder of glycosylation, type IIaa",,,620454,,,,,,,,,,
mondo:0957541,"neurodevelopmental disorder with hypotonia and speech delay, with or without seizures",,,620455,,,,,,,,,,
mondo:0957542,"dystonia 22, adult-onset",,,620456,,,,,,,,,,
mondo:0957543,auriculocondylar syndrome 4,,,620457,,,,,,,,,,
mondo:0957544,auriculocondylar syndrome 2B,,,620458,,,,,,,,,,
mondo:0957545,"cardiomyopathy, dilated, 2I",,,620462,,,,,,,,,,
mondo:0957556,congenital pulmonary vein atresia,,,,99126,,,,,,,,,
mondo:1010000,pythiosis,"['pythium insidiosum infection', 'human pythiosis']",,,,C0276912,,,,D058968,,,,
mondo:1010001,"epilepsy, non-human animal",,,,,,,,,,,,,
mondo:1010002,"myoclonus, non-human animal",,,,,,,,,,,,,
mondo:1010003,"narcolepsy, non-human animal",,,,,,,,,,,,,
mondo:1010004,"paroxysmal dyskinesia, non-human animal",,,,,,,,,,,,,
mondo:1010005,"autism spectrum disorder, non-human animal",,,,,,,,,,,,,
mondo:1010006,"Phelan-McDermid syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010007,"subvalvular aortic stenosis, non-human animal",,,,,,,,,,,,,
mondo:1010008,"atherosclerosis, non-human animal",,,,,,,,,,,,,
mondo:1010009,"atrial septal defect, non-human animal",,,,,,,,,,,,,
mondo:1010010,"cardiomyopathy, non-human animal",,,,,,,,,,,,,
mondo:1010011,"dilated cardiomyopathy, non-human animal",,,,,,,,,,,,,
mondo:1010012,"conotruncal heart malformations, non-human animal",,,,,,,,,,,,,
mondo:1010013,"cor triatriatum dexter, non-human animal",,,,,,,,,,,,,
mondo:1010014,"essential hypertension, non-human animal",,,,,,,,,,,,,
mondo:1010015,"hypertrophic cardiomyopathy, non-human animal",,,,,,,,,,,,,
mondo:1010016,"mitral valve stenosis, non-human animal",,,,,,,,,,,,,
mondo:1010017,"patent ductus arteriosus, non-human animal",,,,,,,,,,,,,
mondo:1010018,"persistent truncus arteriosus, non-human animal",,,,,,,,,,,,,
mondo:1010019,"arrhythmogenic right ventricular cardiomyopathy, non-human animal",,,,,,,,,,,,,
mondo:1010020,"supravalvular aortic stenosis, non-human animal",,,,,,,,,,,,,
mondo:1010021,"tetralogy of fallot, non-human animal",,,,,,,,,,,,,
mondo:1010022,"ventricular septal defect, non-human animal",,,,,,,,,,,,,
mondo:1010023,"patent ductus venosus, non-human animal",,,,,,,,,,,,,
mondo:1010024,"atrial fibrillation, non-human animal",,,,,,,,,,,,,
mondo:1010025,"Wolff-Parkinson-White syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010026,"Budd-Chiari syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010027,"endocardial fibroelastosis, non-human animal",,,,,,,,,,,,,
mondo:1010028,"cerebral amyloid angiopathy, non-human animal",,,,,,,,,,,,,
mondo:1010031,"triploidy, non-human animal",,,,,,,,,,,,,
mondo:1010032,"Jacobsen syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010033,"holoprosencephaly, non-human animal",,,,,,,,,,,,,
mondo:1010034,"cleft lip with or without cleft palate, non-human animal",,,,,,,,,,,,,
mondo:1010035,"mandibulofacial dysostosis, non-human animal",,,,,,,,,,,,,
mondo:1010036,"frontonasal dysplasia, non-human animal",,,,,,,,,,,,,
mondo:1010037,"cleft palate, non-human animal",,,,,,,,,,,,,
mondo:1010038,"gingival hypertrophy, non-human animal",,,,,,,,,,,,,
mondo:1010039,"megacolon, non-human animal",,,,,,,,,,,,,
mondo:1010040,"pyloric stenosis, non-human animal",,,,,,,,,,,,,
mondo:1010041,"Meckel diverticulum, non-human animal",,,,,,,,,,,,,
mondo:1010042,"protein-losing enteropathy, non-human animal",,,,,,,,,,,,,
mondo:1010043,"cystic fibrosis, non-human animal",,,,,,,,,,,,,
mondo:1010044,"microvillus inclusion disease, non-human animal",,,,,,,,,,,,,
mondo:1010045,"diprosopus, non-human animal",,,,,,,,,,,,,
mondo:1010046,"patent urachus, non-human animal",,,,,,,,,,,,,
mondo:1010047,"spina bifida, non-human animal",,,,,,,,,,,,,
mondo:1010048,"spina bifida occulta, non-human animal",,,,,,,,,,,,,
mondo:1010049,"acromegaly, non-human animal",,,,,,,,,,,,,
mondo:1010050,"congenital adrenal hyperplasia, non-human animal",,,,,,,,,,,,,
mondo:1010051,"diabetes insipidus, non-human animal",,,,,,,,,,,,,
mondo:1010052,"diabetes mellitus, non-human animal",,,,,,,,,,,,,
mondo:1010053,"familial goiter, non-human animal",,,,,,,,,,,,,
mondo:1010054,"hyperparathyroidism, non-human animal",,,,,,,,,,,,,
mondo:1010055,"hyperthyroidism, non-human animal",,,,,,,,,,,,,
mondo:1010056,"hypoparathyroidism, non-human animal",,,,,,,,,,,,,
mondo:1010057,"congenital hypothyroidism, non-human animal",,,,,,,,,,,,,
mondo:1010058,"exocrine pancreatic insufficiency, non-human animal",,,,,,,,,,,,,
mondo:1010059,"thyroiditis, non-human animal",,,,,,,,,,,,,
mondo:1010060,"pheochromocytoma, non-human animal",,,,,,,,,,,,,
mondo:1010061,"hyperaldosteronism, non-human animal",,,,,,,,,,,,,
mondo:1010062,"congenital adrenal hyperplasia due to 11-beta hydroxylase deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010063,"congenital adrenal hypoplasia, non-human animal",,,,,,,,,,,,,
mondo:1010066,"microcephaly, non-human animal",,,,,,,,,,,,,
mondo:1010067,"omphalocele, non-human animal",,,,,,,,,,,,,
mondo:1010068,"situs inversus, non-human animal",,,,,,,,,,,,,
mondo:1010069,"autoimmune thrombocytopenia, non-human animal",,,,,,,,,,,,,
mondo:1010070,"Chediak-Higashi syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010071,"factor VII deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010072,"factor X deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010073,"factor XI deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010074,"factor XII deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010075,"hemophilia B, non-human animal",,,,,,,,,,,,,
mondo:1010076,"hypereosinophilic syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010077,"Pelger-Huet anomaly, non-human animal",,,,,,,,,,,,,
mondo:1010078,"polycythemia, non-human animal",,,,,,,,,,,,,
mondo:1010079,"prekallikrein deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010080,"thrombocytopenia, non-human animal",,,,,,,,,,,,,
mondo:1010081,"autoimmune thrombocytopenic purpura, non-human animal",,,,,,,,,,,,,
mondo:1010082,"Evans syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010083,"Scott Syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010085,"factor XIII deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010086,"myeloperoxidase deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010090,"anotia, non-human animal",,,,,,,,,,,,,
mondo:1010091,"microtia, non-human animal",,,,,,,,,,,,,
mondo:1010092,"AA amyloidosis, non-human animal",,,,,,,,,,,,,
mondo:1010093,"AL amyloidosis, non-human animal",,,,,,,,,,,,,
mondo:1010094,"analphalipoproteinaemia, non-human animal",,,,,,,,,,,,,
mondo:1010095,"citrullinemia, non-human animal",,,,,,,,,,,,,
mondo:1010099,"pyruvate kinase deficiency of erythrocyte, non-human animal",,,,,,,,,,,,,
mondo:1010101,"galactosemia, non-human animal",,,,,,,,,,,,,
mondo:1010102,"porphyria cutanea tarda, non-human animal",,,,,,,,,,,,,
mondo:1010103,"eclampsia, non-human animal",,,,,,,,,,,,,
mondo:1010104,"trimethylaminuria (fishy taint), non-human animal",,,,,,,,,,,,,
mondo:1010105,"pyruvate dehydrogenase deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010106,"multiple acyl-coa dehydrogenase deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010107,"acute intermittent porphyria, non-human animal",,,,,,,,,,,,,
mondo:1010109,"dihydropyrimidinase deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010110,"hyperphosphatemia, non-human animal",,,,,,,,,,,,,
mondo:1010113,"glucocorticoid resistance, non-human animal",,,,,,,,,,,,,
mondo:1010114,"phenylketonuria, non-human animal",,,,,,,,,,,,,
mondo:1010115,"c8 deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010118,"systemic lupus erythematosus, non-human animal",,,,,,,,,,,,,
mondo:1010119,"scleroderma, non-human animal",,,,,,,,,,,,,
mondo:1010121,"periodic fever syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010123,"common variable immunodeficiency, non-human animal",,,,,,,,,,,,,
mondo:1010124,"autoimmune lymphoproliferative syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010126,"atopic dermatitis, non-human animal",,,,,,,,,,,,,
mondo:1010127,"dermatomyositis, non-human animal",,,,,,,,,,,,,
mondo:1010129,"epidermolysis bullosa, non-human animal",,,,,,,,,,,,,
mondo:1010130,"hypertrichosis, non-human animal",,,,,,,,,,,,,
mondo:1010133,"acrodermatitis enteropathica, non-human animal",,,,,,,,,,,,,
mondo:1010134,"pityriasis rosea, non-human animal",,,,,,,,,,,,,
mondo:1010135,"protoporphyria, non-human animal",,,,,,,,,,,,,
mondo:1010136,"vitiligo, non-human animal",,,,,,,,,,,,,
mondo:1010137,"bullous pemphigoid, non-human animal",,,,,,,,,,,,,
mondo:1010138,"pemphigus, non-human animal",,,,,,,,,,,,,
mondo:1010139,"atrichia with papular lesions, non-human animal",,,,,,,,,,,,,
mondo:1010140,"alopecia areata, non-human animal",,,,,,,,,,,,,
mondo:1010141,"ectodermal dysplasia/skin fragility syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010142,"pyoderma, non-human animal",,,,,,,,,,,,,
mondo:1010143,"incontinentia pigmenti, non-human animal",,,,,,,,,,,,,
mondo:1010147,"stiff skin syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010149,"tricho-dento-osseous-like syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010153,"Darier disease, non-human animal",,,,,,,,,,,,,
mondo:1010155,"cutis laxa, non-human animal",,,,,,,,,,,,,
mondo:1010156,"brachydactyly, non-human animal",,,,,,,,,,,,,
mondo:1010157,"hyperostosis, non-human animal",,,,,,,,,,,,,
mondo:1010158,"polydactyly, non-human animal",,,,,,,,,,,,,
mondo:1010159,"split hand, non-human animal",,,,,,,,,,,,,
mondo:1010160,"syndactyly, non-human animal",,,,,,,,,,,,,
mondo:1010161,"tibial hemimelia, non-human animal",,,,,,,,,,,,,
mondo:1010162,"radial hemimelia, non-human animal",,,,,,,,,,,,,
mondo:1010163,"tetradysmelia, non-human animal",,,,,,,,,,,,,
mondo:1010164,"Wilson disease, non-human animal",,,,,,,,,,,,,
mondo:1010166,"galactosialidosis, non-human animal",,,,,,,,,,,,,
mondo:1010167,"gangliosidosis, non-human animal",,,,,,,,,,,,,
mondo:1010170,"Krabbe disease, non-human animal",,,,,,,,,,,,,
mondo:1010171,"lysosomal storage disease, non-human animal",,,,,,,,,,,,,
mondo:1010172,"alpha-mannosidosis, non-human animal",,,,,,,,,,,,,
mondo:1010191,"deficiency of uridine monophosphate synthase, non-human animal",,,,,,,,,,,,,
mondo:1010192,"central core myopathy, non-human animal",,,,,,,,,,,,,
mondo:1010195,"myopathy, non-human animal",,,,,,,,,,,,,
mondo:1010196,"congenital myopathy, non-human animal",,,,,,,,,,,,,
mondo:1010197,"myositis ossificans, non-human animal",,,,,,,,,,,,,
mondo:1010198,"myotonic dystrophy, non-human animal",,,,,,,,,,,,,
mondo:1010199,"muscular dystrophy, Duchenne type, non-human animal",,,,,,,,,,,,,
mondo:1010201,"congenital pseudomyotonia, non-human animal",,,,,,,,,,,,,
mondo:1010202,"myotubular myopathy 1, non-human animal",,,,,,,,,,,,,
mondo:1010203,"polymyositis, non-human animal",,,,,,,,,,,,,
mondo:1010208,"myofibrillar myopathy, non-human animal",,,,,,,,,,,,,
mondo:1010209,"lymphosarcoma, non-human animal",,,,,,,,,,,,,
mondo:1010210,"malignant histiocytosis, non-human animal",,,,,,,,,,,,,
mondo:1010211,"mycosis fungoides, non-human animal",,,,,,,,,,,,,
mondo:1010212,"osteosarcoma, non-human animal",,,,,,,,,,,,,
mondo:1010213,"chronic monocytic leukemia, non-human animal",,,,,,,,,,,,,
mondo:1010214,"non-hodgkin lymphoma, non-human animal",,,,,,,,,,,,,
mondo:1010215,"familial adenomatous polyposis, non-human animal",,,,,,,,,,,,,
mondo:1010216,"embryonal rhabdomyosarcoma, non-human animal",,,,,,,,,,,,,
mondo:1010217,"schwannomatosis, non-human animal",,,,,,,,,,,,,
mondo:1010220,"ameloblastoma, non-human animal",,,,,,,,,,,,,
mondo:1010222,"chronic myelomonocytic leukemia, non-human animal",,,,,,,,,,,,,
mondo:1010223,"prostate cancer, non-human animal",,,,,,,,,,,,,
mondo:1010224,"benign prostatic hyperplasia, non-human animal",,,,,,,,,,,,,
mondo:1010225,"cystic hygroma, non-human animal",,,,,,,,,,,,,
mondo:1010226,"lymphangiosarcoma, non-human animal",,,,,,,,,,,,,
mondo:1010227,"cauda equina syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010228,"Dandy-Walker syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010229,"dysautonomia, non-human animal",,,,,,,,,,,,,
mondo:1010230,"hepatic encephalopathy, non-human animal",,,,,,,,,,,,,
mondo:1010231,"Huntington disease, non-human animal",,,,,,,,,,,,,
mondo:1010232,"hydranencephaly, non-human animal",,,,,,,,,,,,,
mondo:1010233,"hydrocephalus, non-human animal",,,,,,,,,,,,,
mondo:1010234,"olivopontocerebellar atrophy, non-human animal",,,,,,,,,,,,,
mondo:1010235,"spinal muscular atrophy, non-human animal",,,,,,,,,,,,,
mondo:1010236,"syringomyelia, non-human animal",,,,,,,,,,,,,
mondo:1010237,"polymicrogyria, non-human animal",,,,,,,,,,,,,
mondo:1010238,"leukodystrophy, non-human animal",,,,,,,,,,,,,
mondo:1010239,"peripheral neuropathy, non-human animal",,,,,,,,,,,,,
mondo:1010240,"Horner syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010241,"giant axonal neuropathy, non-human animal",,,,,,,,,,,,,
mondo:1010242,"Alexander disease, non-human animal",,,,,,,,,,,,,
mondo:1010243,"cerebellar degeneration, non-human animal",,,,,,,,,,,,,
mondo:1010244,"L-2-hydroxyglutaricacidemia, non-human animal",,,,,,,,,,,,,
mondo:1010245,"hyperekplexia, non-human animal",,,,,,,,,,,,,
mondo:1010247,"lissencephaly and cerebellar hypoplasia, non-human animal",,,,,,,,,,,,,
mondo:1010249,"ataxia telangiectasia, non-human animal",,,,,,,,,,,,,
mondo:1010252,"succinic semialdehyde dehydrogenase deficiency, non-human animal",,,,,,,,,,,,,
mondo:1010258,"glomerulonephritis, non-human animal",,,,,,,,,,,,,
mondo:1010259,"nephritis, non-human animal",,,,,,,,,,,,,
mondo:1010260,"nephrolithiasis, non-human animal",,,,,,,,,,,,,
mondo:1010261,"nephrotic syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010262,"polycystic kidney disease, non-human animal",,,,,,,,,,,,,
mondo:1010264,"renal hypoplasia, non-human animal",,,,,,,,,,,,,
mondo:1010265,"renal hypoplasia, unilateral, non-human animal",,,,,,,,,,,,,
mondo:1010266,"renal hypoplasia, bilateral, non-human animal",,,,,,,,,,,,,
mondo:1010267,"urolithiasis, non-human animal",,,,,,,,,,,,,
mondo:1010268,"renal dysplasia, non-human animal",,,,,,,,,,,,,
mondo:1010269,"hypospadias, non-human animal",,,,,,,,,,,,,
mondo:1010270,"alkaptonuria, non-human animal",,,,,,,,,,,,,
mondo:1010272,"renal agenesis, non-human animal",,,,,,,,,,,,,
mondo:1010275,"cryptorchidism, non-human animal",,,,,,,,,,,,,
mondo:1010276,"hypogonadism, non-human animal",,,,,,,,,,,,,
mondo:1010277,"orchitis, non-human animal",,,,,,,,,,,,,
mondo:1010278,"persistent Mullerian duct syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010279,"hymen, imperforate, non-human animal",,,,,,,,,,,,,
mondo:1010280,"priapism, non-human animal",,,,,,,,,,,,,
mondo:1010281,"testicular regression syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010282,"azoospermia, non-human animal",,,,,,,,,,,,,
mondo:1010284,"allergic rhinitis, non-human animal",,,,,,,,,,,,,
mondo:1010285,"atrophic rhinitis, non-human animal",,,,,,,,,,,,,
mondo:1010286,"pneumothorax, non-human animal",,,,,,,,,,,,,
mondo:1010287,"pulmonary hypertension, non-human animal",,,,,,,,,,,,,
mondo:1010289,"choanal atresia, non-human animal",,,,,,,,,,,,,
mondo:1010290,"pulmonary agenesis, non-human animal",,,,,,,,,,,,,
mondo:1010291,"achondroplasia, non-human animal",,,,,,,,,,,,,
mondo:1010292,"ankylosing spondylitis, non-human animal",,,,,,,,,,,,,
mondo:1010293,"anodontia, non-human animal",,,,,,,,,,,,,
mondo:1010294,"rheumatoid arthritis, non-human animal",,,,,,,,,,,,,
mondo:1010295,"osteoporosis, non-human animal",,,,,,,,,,,,,
mondo:1010296,"Marfan syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010297,"osteoarthritis, non-human animal",,,,,,,,,,,,,
mondo:1010298,"osteochondritis dissecans, non-human animal",,,,,,,,,,,,,
mondo:1010299,"osteochondrosis, non-human animal",,,,,,,,,,,,,
mondo:1010300,"osteopetrosis, non-human animal",,,,,,,,,,,,,
mondo:1010302,"scoliosis, non-human animal",,,,,,,,,,,,,
mondo:1010303,"spinal stenosis, non-human animal",,,,,,,,,,,,,
mondo:1010304,"synovial chondromatosis, non-human animal",,,,,,,,,,,,,
mondo:1010305,"craniosynostosis, non-human animal",,,,,,,,,,,,,
mondo:1010306,"osteochondrodysplasia, non-human animal",,,,,,,,,,,,,
mondo:1010310,"schmid metaphyseal chondrodysplasia dwarfism, non-human animal",,,,,,,,,,,,,
mondo:1010312,"osteopetrosis with gingival hamartomas, non-human animal",,,,,,,,,,,,,
mondo:1010313,"spondylocostal dysostosis, autosomal recessive, non-human animal",,,,,,,,,,,,,
mondo:1010314,"Van den Ende-Gupta syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010315,"periodontitis, non-human animal",,,,,,,,,,,,,
mondo:1010316,"hypophosphatasia, non-human animal",,,,,,,,,,,,,
mondo:1010318,"GAPO syndrome, non-human animal",,,,,,,,,,,,,
mondo:1010319,"coloboma, non-human animal",,,,,,,,,,,,,
mondo:1010320,"corneal dystrophy, non-human animal",,,,,,,,,,,,,
mondo:1010321,"retinal detachment, non-human animal",,,,,,,,,,,,,
mondo:1010322,"ectropion, non-human animal",,,,,,,,,,,,,
mondo:1010323,"entropion, non-human animal",,,,,,,,,,,,,
mondo:1010324,"microphthalmia, non-human animal",,,,,,,,,,,,,
mondo:1010325,"congenital nystagmus, non-human animal",,,,,,,,,,,,,
mondo:1010326,"retinal degeneration, non-human animal",,,,,,,,,,,,,
mondo:1010327,"strabismus, non-human animal",,,,,,,,,,,,,
mondo:1010328,"retinoschisis, non-human animal",,,,,,,,,,,,,
mondo:1010329,"Leber congenital amaurosis, non-human animal",,,,,,,,,,,,,
mondo:1010330,"keratitis, non-human animal",,,,,,,,,,,,,
mondo:1010334,"retinitis pigmentosa, non-human animal",,,,,,,,,,,,,
mondo:1010337,"myopia, non-human animal",,,,,,,,,,,,,
mondo:1010343,"diabetic cataract, non-human animal",,,,,,,,,,,,,
mondo:1010344,"Peters anomaly, non-human animal",,,,,,,,,,,,,
mondo:1010350,"macular corneal dystrophy, non-human animal",,,,,,,,,,,,,
mondo:1010351,"age-related macular degeneration, non-human animal",,,,,,,,,,,,,
mondo:1010352,"microphthalmia, isolated, with coloboma, non-human animal",,,,,,,,,,,,,
mondo:1010358,"Leber hereditary optic neuropathy, non-human animal",,,,,,,,,,,,,
mondo:1010359,"night blindness, non-human animal",,,,,,,,,,,,,
mondo:1010360,"dacryocystitis, non-human animal",,,,,,,,,,,,,
mondo:1010361,"hyperphagia leading to hepatic steatosis, non-human animal",,,,,,,,,,,,,
mondo:1011300,"acute disease, non-human animal",,,,,,,,,,,,,
mondo:1011301,"auditory system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011302,"branchial arch disease, non-human animal",,,,,,,,,,,,,
mondo:1011303,"mammary gland disorder, non-human animal",,,,,,,,,,,,,
mondo:1011304,"mammary fibrocystic disease, non-human animal",,,,,,,,,,,,,
mondo:1011305,"cancer or benign tumor, non-human animal",,,,,,,,,,,,,
mondo:1011306,"cardiovascular disorder, non-human animal",,,,,,,,,,,,,
mondo:1011307,"chromosomal disorder, non-human animal",,,,,,,,,,,,,
mondo:1011308,"congenital nervous system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011309,"connective tissue disorder, non-human animal",,,,,,,,,,,,,
mondo:1011310,"developmental defect during embryogenesis, non-human animal",,,,,,,,,,,,,
mondo:1011311,"digestive system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011312,"disease related to transplantation, non-human animal",,,,,,,,,,,,,
mondo:1011313,"disorder of development or morphogenesis, non-human animal",,,,,,,,,,,,,
mondo:1011314,"disorder of glycosylation, non-human animal",,,,,,,,,,,,,
mondo:1011315,"disorder of orbital region, non-human animal",,,,,,,,,,,,,
mondo:1011316,"disorder of visual system, non-human animal",,,,,,,,,,,,,
mondo:1011317,"endocrine system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011318,"hearing disorder, non-human animal",,,,,,,,,,,,,
mondo:1011319,"hematologic disorder, non-human animal",,,,,,,,,,,,,
mondo:1011321,"hereditary disease, non-human animal",,,,,,,,,,,,,
mondo:1011322,"iatrogenic disease, non-human animal",,,,,,,,,,,,,
mondo:1011323,"idiopathic disease, non-human animal",,,,,,,,,,,,,
mondo:1011325,"immunodeficiency-related disorder, non-human animal",,,,,,,,,,,,,
mondo:1011327,"inflammatory disease, non-human animal",,,,,,,,,,,,,
mondo:1011328,"integumentary system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011329,"keratoconjunctivitis, non-human animal",,,,,,,,,,,,,
mondo:1011330,"lymphoid system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011331,"metabolic disease, non-human animal",,,,,,,,,,,,,
mondo:1011332,"mitochondrial disease, non-human animal",,,,,,,,,,,,,
mondo:1011333,"mouth disorder, non-human animal",,,,,,,,,,,,,
mondo:1011334,"mouth mucosa disorder, non-human animal",,,,,,,,,,,,,
mondo:1011335,"musculoskeletal system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011336,"nervous system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011337,"neurocristopathy, non-human animal",,,,,,,,,,,,,
mondo:1011338,"nutritional disorder, non-human animal",,,,,,,,,,,,,
mondo:1011339,"obstetric disorder, non-human animal",,,,,,,,,,,,,
mondo:1011340,"occupational disorder, non-human animal",,,,,,,,,,,,,
mondo:1011341,"omphalitis, non-human animal",,,,,,,,,,,,,
mondo:1011342,"otorhinolaryngologic disease, non-human animal",,,,,,,,,,,,,
mondo:1011343,"perceptual disorders, non-human animal",,,,,,,,,,,,,
mondo:1011344,"perinatal disease, non-human animal",,,,,,,,,,,,,
mondo:1011345,"poisoning, non-human animal",,,,,,,,,,,,,
mondo:1011346,"post-bacterial disorder, non-human animal",,,,,,,,,,,,,
mondo:1011347,"post-COVID-19 disorder, non-human animal",,,,,,,,,,,,,
mondo:1011348,"post-infectious disorder, non-human animal",,,,,,,,,,,,,
mondo:1011349,"post-viral disorder, non-human animal",,,,,,,,,,,,,
mondo:1011350,"premature aging syndrome, non-human animal",,,,,,,,,,,,,
mondo:1011351,"psychiatric disorder, non-human animal",,,,,,,,,,,,,
mondo:1011352,"radiation-induced disorder, non-human animal",,,,,,,,,,,,,
mondo:1011353,"radiculitis, non-human animal",,,,,,,,,,,,,
mondo:1011354,"reproductive system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011356,"sensory ganglionopathy, non-human animal",,,,,,,,,,,,,
mondo:1011357,"serositis, non-human animal",,,,,,,,,,,,,
mondo:1011358,"skin appendage disorder, non-human animal",,,,,,,,,,,,,
mondo:1011359,"subcutaneous tissue disorder, non-human animal",,,,,,,,,,,,,
mondo:1011360,"syndromic disease, non-human animal",,,,,,,,,,,,,
mondo:1011361,"thymus gland disorder, non-human animal",,,,,,,,,,,,,
mondo:1011363,"ulcer disease, non-human animal",,,,,,,,,,,,,
mondo:1011364,"upper digestive tract disorder, non-human animal",,,,,,,,,,,,,
mondo:1011365,"urinary system disorder, non-human animal",,,,,,,,,,,,,
mondo:1011367,"vision disorder, non-human animal",,,,,,,,,,,,,
mondo:8000000,infectious discitis,,,,,,,,,,,,,
mondo:8000001,staphylococcus discitis,,,,,,,,,,,,,
mondo:8000002,escherichia coli discitis,,,,,,,,,,,,,
mondo:8000003,streptococcus pneumoniae discitis,,,,,,,,,,,,,
mondo:8000004,salmonella discitis,,,,,,,,,,,,,
mondo:8000005,fungal discitis,,,,,,,,,,,,,
mondo:8000006,WHIM syndrome 1,"['Warts, hypogammaglobulinemia, infections, and myelokathexis', 'WHIM syndrome', 'Warts, hypogammaglobulinemia, infections, and myelokathexis syndrome', 'Warts-hypogammaglobulinemia-infections-myelokathexis syndrome', 'myelokathexis, isolated', 'Warts-infections-leukopenia-myelokatexis syndrome', 'WILM', 'WHIMS']",0060591,193670,51636,C0472817,"['-0.02156', '0.04132', '0.000224', '-0.012344', '0.00268', '-0.0596', '-0.001231', '0.05084', '-0.03198', '-0.01917', '-0.02003', '-0.01205', '-0.006355', '0.0105', '-0.02544', '-0.02237', '-0.011604', '-0.009224', '-0.02696', '-0.0756', '0.00975', '-0.02666', '0.03668', '-0.01978', '0.02151', '-0.01117', '-0.01857', '-0.01429', '0.0159', '-0.02275', '0.05096', '-0.01372', '0.0681', '0.02597', '-0.00984', '-0.02496', '-0.001139', '-0.02756', '-0.002413', '-0.0447', '0.01706', '-0.03595', '0.012276', '-0.01572', '0.002115', '-0.03302', '-0.03552', '0.03513', '0.01935', '0.02032', '-0.02536', '0.02216', '0.0063', '-0.01288', '-0.010735', '-0.005306', '0.03043', '-0.0159', '-0.04623', '0.006516', '0.01555', '0.00845', '0.002728', '-0.01203', '-0.0005116', '0.00917', '0.05328', '0.02882', '-0.04108', '0.04907', '-0.042', '0.00911', '0.004898', '-0.01556', '0.02246', '0.01724', '-0.001337', '-0.00474', '-0.02267', '-0.00768', '0.007965', '0.003473', '-0.00569', '0.02435', '-0.005306', '-0.014656', '0.02417', '0.05182', '0.05286', '0.00723', '0.02307', '0.02267', '-0.002077', '0.01443', '0.0841', '0.0374', '0.02089', '-0.05386', '-0.00866', '0.02632']",,,C536697,,,,
mondo:8000008,Martsolf syndrome 1,"['MARTSOLF syndrome', 'cataract-intellectual disability-hypogonadism syndrome', 'cataract-intellectual disability-hypogonadism', 'cataract-mental retardation-hypogonadism', 'Martsolf syndrome']",0111586,212720,1387,C0796037,"['-0.1023', '0.0907', '0.07697', '-0.0842', '0.03253', '-0.1437', '0.03004', '0.2332', '-0.1276', '-0.1178', '-0.05396', '-0.079', '0.00794', '-0.052', '-0.02885', '-0.0497', '0.0349', '-0.03293', '-0.1023', '-0.303', '-0.0377', '0.007133', '-0.02551', '-0.0435', '0.1009', '0.000496', '-0.08716', '0.0399', '0.0892', '-0.10583', '0.1448', '0.02531', '0.2324', '0.05264', '0.0811', '-0.08777', '-0.0678', '-0.2162', '-0.06323', '-0.1433', '0.1233', '-0.09735', '-0.01211', '0.01215', '-0.01195', '-0.0887', '-0.0206', '0.0835', '-0.048', '-0.0468', '-0.05396', '0.01828', '0.04712', '-0.0953', '-0.0632', '-0.02359', '0.1376', '-0.0568', '-0.1505', '0.09174', '0.05713', '-0.00373', '0.0392', '0.02063', '-0.0938', '0.04364', '0.1473', '0.2142', '-0.1526', '0.03253', '-0.1794', '0.03726', '0.03738', '-0.1014', '0.0578', '-0.03296', '0.08246', '-0.0792', '-0.1103', '0.02002', '0.02632', '0.07025', '-0.0986', '0.171', '0.0353', '0.063', '0.0323', '0.1388', '0.11865', '0.11017', '0.10535', '0.1945', '0.03632', '-0.00151', '0.2922', '-0.004196', '0.1187', '-0.1832', '0.0875', '0.1157']",,,C536028,,,,
mondo:8000010,antiphospholipid syndrome,"['Hughes syndrome', 'antiphospholipid antibody syndrome', 'antiphospholipid syndrome', 'lupus anticoagulant, familial', 'familial lupus anticoagulant']",2988,,80,C0085278,,C61283,,D016736,279.49,D68.61,,
mondo:8000011,"visceral neuropathy, familial, 1, autosomal recessive","['NID A', 'visceral neuropathy familial', 'pseudoobstruction chronic idiopathic intestinal neuronal type', 'intestinal pseudoobstruction due to neuronal disease', 'Argyrophil myenteric plexus deficiency of', 'Argyrophil myenteric plexus, deficiency of', 'neuronal intestinal dysplasia, type a', 'visceral neuropathy, familial, autosomal recessive', 'pseudoobstruction, chronic idiopathic intestinal, neuronal type']",0080679,243180,99811,C1855733,,,,C537394,,,,
mondo:8000012,"neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 1","['infantile-onset multisystem neurologic, endocrine, and pancreatic disease', 'IMNEPD', 'neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset']",,616263,456312,C4015728,,,,,,,,
mondo:8000013,"portal hypertension, noncirrhotic, 1","['NCPH', 'portal hypertension, noncirrhotic']",,617068,,C4310735,,,,,,,,
mondo:8000014,familial antiphospholipid syndrome,"['Hughes syndrome', 'antiphospholipid syndrome, familial']",,107320,,C2930802,,,,C531622,,,,
mondo:8000015,"46,XY sex reversal 11","['anorchia, familial', 'testicular regression syndrome', 'XY gonadal agenesis syndrome', 'SRXY11', 'embryonic testicular regression syndrome', 'TRS', '46, XY sex reversal 11', 'ETRS', 'vanishing testes syndrome', 'testicular regression, embryonic', 'vanishing testis syndrome']",,273250,983,C0266427,"['-0.02856', '0.06775', '0.01435', '-0.0597', '0.02469', '-0.1471', '0.0339', '0.0974', '-0.08856', '-0.02473', '-0.02573', '-0.01938', '-0.02216', '-0.002733', '-0.03108', '-0.086', '-0.02765', '-0.04028', '-0.04706', '-0.1478', '-0.01833', '-0.05557', '0.01692', '-0.0847', '0.08765', '-0.05655', '0.02478', '-0.00879', '-0.04514', '-0.0655', '0.0873', '0.002935', '0.1451', '0.006004', '-0.00982', '-0.01512', '-0.01259', '-0.06433', '-0.0396', '-0.0941', '0.08673', '-0.0837', '0.01052', '-0.02061', '-0.002518', '-0.05908', '-0.03824', '0.02539', '0.00777', '0.07446', '-0.04855', '-0.02333', '-0.02779', '0.01805', '0.0105', '0.014854', '0.099', '-0.039', '-0.1102', '0.03574', '0.1011', '0.0194', '0.02487', '0.02603', '-6.43e-05', '-0.002808', '0.1172', '0.0768', '-0.11017', '0.0982', '-0.10803', '0.06836', '0.010216', '-0.0762', '0.02356', '0.01398', '0.0175', '0.004814', '-0.0996', '-0.05554', '-0.00857', '0.02054', '-0.05045', '0.0659', '-0.03235', '-0.01357', '0.02113', '0.0556', '0.08594', '-0.03568', '0.00944', '0.11035', '-0.004505', '0.01491', '0.1343', '0.02539', '0.0959', '-0.1171', '0.02245', '0.04834']",,,C537770,752.89,,10002641,
mondo:8000018,benign paroxysmal positional vertigo,"['benign paroxysmal positional vertigo', 'vestibulopathy, familial', 'vertigo, benign paroxysmal positional', 'familial benign recurrent vertigo', 'benign paroxysmal positional nystagmus', 'BPPV', 'vertigo, benign recurrent', 'BRV', 'familial vestibulopathy']",13941,193007,,C0155502,,,,D065635,386.11,,,
mondo:8000019,"vertigo, benign recurrent, 1","['vertigo, benign recurrent, 1', 'BRV1']",,,,,,,,C567620,,,,
mondo:8000023,type 3 autoimmune lymphoproliferative syndrome,,,,,C1519711,,C39577,,,,,,
mondo:8000024,"autoimmune lymphoproliferative syndrome, type III caused by mutation in PRKCD",,0110119,615559,,C3809928,,,,,,,,
mondo:0015063,"duodenal neuroendocrine tumor, well differentiated, low or intermediate grade","['duodenal neuroendocrine tumor', 'duodenal neuroendocrine tumour']",,,100076,CN197356,,C135080,,,,,,
mondo:0015064,"jejunal neuroendocrine tumor, well differentiated, low or intermediate grade","['jejunal neuroendocrine tumor', 'jejunal neuroendocrine tumour', 'jejunal neuroendocrine neoplasm']",,,100077,CN197357,,C135090,,,,,,
mondo:0015065,"ileal neuroendocrine tumor, well differentiated, low or intermediate grade","['ileal neuroendocrine tumour', 'ileal neuroendocrine tumor', 'ileal neuroendocrine neoplasm']",,,100078,CN197358,,C135092,,,,,,
mondo:0015066,"neuroendocrine tumor of the appendix, well differentiated, low or intermediate grade","['appendix well differentiated endocrine tumour', 'appendiceal NEN', 'NEN of appendix', 'appendiceal neuroendocrine tumor', 'appendix neuroendocrine tumor', 'appendix neuroendocrine tumour', 'appendix well differentiated endocrine tumor', 'appendiceal neuroendocrine neoplasm', 'well-differentiated neuroendocrine tumor of the appendix', 'appendiceal neuroendocrine tumour', 'appendix NET', 'appendix well differentiated endocrine tumor/carcinoma', 'neuroendocrine neoplasm of appendix', 'well-differentiated neuroendocrine tumour of the appendix']",,,100079,,,C96422,,,,,,
mondo:0015067,"neuroendocrine tumor of the colon, well differentiated, low or intermediate grade tumor","['colon neuroendocrine tumor', 'NET of the colon', 'colon neuroendocrine tumour', 'carcinoid tumour of colon', 'colonic NET', 'neuroendocrine neoplasm of the colon', 'carcinoid tumor of colon']",,,,,,C135212,,,,,,
mondo:0015068,"neuroendocrine tumor of rectum, well differentiated, low or intermediate grade","['neuroendocrine tumor of the rectum', 'rectal neuroendocrine tumour', 'neuroendocrine tumour of the rectum', 'rectal neuroendocrine tumor']",,,,CN197361,,C135213,,,,,,
mondo:0015069,neuroendocrine tumor of the anal canal,"['anal canal well differentiated tumor', 'NET of the anal canal', 'anal canal well differentiated tumour', 'neuroendocrine tumor of anal canal', 'anal canal well differentiated tumor/carcinoma', 'anal Neuroendocrine tumor', 'anal Neuroendocrine tumour', 'anal canal neuroendocrine tumour', 'anal canal neuroendocrine tumor', 'anal NET', 'NET of anal canal', 'anal canal neuroendocrine neoplasm', 'neuroendocrine tumour of anal canal', 'anal canal NET', 'neuroendocrine neoplasm of the anal canal']",,,100082,CN197362,,C96540,,,,,,
mondo:0015070,laryngeal neuroendocrine neoplasm,"['laryngeal neuroendocrine neoplasm', 'neuroendocrine neoplasm of larynx', 'neuroendocrine tumor of larynx', 'larynx neuroendocrine tumor', 'neuroendocrine tumour of larynx', 'larynx neuroendocrine tumor, well differentiated, low or intermediate grade', 'larynx NET', 'laryngeal neuroendocrine tumor', 'neuroendocrine neoplasm of the larynx', 'laryngeal neuroendocrine tumour', 'larynx neuroendocrine neoplasm', 'larynx neuroendocrine tumour']",5457,,100083,C1334374,,C6023,,,,,,
mondo:0015071,middle ear neuroendocrine tumor,"['middle ear neuroendocrine neoplasm', 'middle ear NET', 'middle ear neuroendocrine tumor', 'neuroendocrine neoplasm of middle ear', 'neuroendocrine tumour of middle ear', 'middle ear neuroendocrine tumor, well differentiated, low or intermediate grade']",,,100084,CN197364,,,,,,,,
mondo:0015072,liver neuroendocrine carcinoma,"['HNEC', 'primary hepatic neuroendocrine carcinoma', 'primary liver neuroendocrine carcinoma', 'liver neuroendocrine carcinoma', 'liver neuroendocrine cancer', 'PHNEC', 'neuroendocrine carcinoma of liver', 'hepatic neuroendocrine carcinoma']",,,100085,CN197365,,C96787,,,,,,
mondo:0015073,"gallbladder neuroendocrine tumor, grade 1/2","['gallbladder neuroendocrine tumor', 'gallbladder NET', 'gallbladder neuroendocrine tumour', 'gallbladder well differentiated endocrine tumour', 'gallbladder well differentiated endocrine tumor', 'gallbladder well differentiated endocrine tumor/carcinoma']",,,100086,CN197366,,C96918,,,,,,
mondo:0015074,thyroid tumor,"['thyroid gland tumor', 'neoplasm of thyroid', 'tumour of the thyroid', 'tumor of the thyroid', 'tumour of thyroid gland', 'tumor of thyroid', 'thyroid tumor', 'thyroid gland tumour', 'tumour of thyroid', 'tumor of the thyroid gland', 'thyroid neoplasms', 'thyroid neoplasm', 'neoplasm of thyroid gland', 'neoplasm of the thyroid', 'neoplasm of the thyroid gland', 'thyroid gland neoplasm (disease)', 'thyroid gland neoplasm', 'THYROID', 'tumour of the thyroid gland', 'tumor of thyroid gland']",,,100087,,,C3414,0003841,,239.7,,,
mondo:0015075,thyroid gland carcinoma,"['head and neck cancer, thyroid', 'thyroid gland carcinoma', 'cancer of thyroid', 'carcinoma of the thyroid gland', 'thyroid gland cancer', 'thyroid carcinoma', 'carcinoma of the thyroid', 'cancer of the thyroid', 'thyroid cancer', 'carcinoma of thyroid', 'carcinoma of thyroid gland']",3963,,100088,C0549473,,C4815,1000586,,,,10007476,0002890
mondo:0015079,multiple polyglandular tumor,,,,100094,CN197373,,,,,,,,
mondo:0015082,alopecia antibody deficiency,['IPP-Gelfand syndrome'],,,1006,,,,,,,,,
mondo:0015083,nuclear oculomotor paralysis,,,,100932,,,,,,,,,
mondo:0015084,FRAXF syndrome,,,,100974,CN197382,,,,,,,,
mondo:0015085,bathing suit ichthyosis,['BSI'],,,100976,C4511230,,,,,,,,
mondo:0015086,cloverleaf skull-asphyxiating thoracic dysplasia syndrome,"['Benallegue Lacete syndrome', 'cloverleaf skull and asphyxiating thoracic dysplasia', 'Benallegue-Lacete syndrome']",,,100978,CN197384,,,,,,,,
mondo:0015087,autosomal dominant complex spastic paraplegia,"['autosomal dominant complex HSP', 'autosomal dominant complex SPG', 'autosomal dominant complex hereditary spastic paraplegia', 'autosomal dominant complicated HSP', 'autosomal dominant complicated SPG', 'autosomal dominant complicated spastic paraplegia', 'complex hereditary spastic paraplegia, autosomal dominant']",,,100979,CN226593,,,,,,,,
mondo:0015088,autosomal dominant pure spastic paraplegia,"['autosomal dominant pure HSP', 'pure hereditary spastic paraplegia, autosomal dominant', 'autosomal dominant uncomplicated SPG', 'autosomal dominant pure SPG', 'autosomal dominant pure hereditary spastic paraplegia', 'autosomal dominant uncomplicated HSP', 'autosomal dominant uncomplicated spastic paraplegia']",,,100980,CN226594,"['-0.01872', '0.209', '-0.1433', '-0.235', '-0.1752', '-0.669', '-0.2893', '0.00708', '-0.3196', '-0.4036', '-0.01762', '-0.1417', '-0.003689', '0.4678', '0.7163', '0.1543', '-0.3975', '-0.224', '0.1825', '-0.427', '0.1517', '-0.2708', '0.2576', '0.2163', '0.06015', '-0.04315', '0.1522', '-0.1025', '-0.1179', '-0.2673', '0.275', '0.1847', '0.1039', '0.3218', '0.1101', '-0.3843', '-0.14', '-0.344', '-0.2025', '-0.2437', '-0.07306', '-0.672', '-0.06915', '0.2537', '-0.00753', '-0.4675', '-0.3086', '0.3557', '0.03772', '0.1636', '-0.02222', '-0.015335', '-0.2375', '-0.1884', '0.0921', '-0.6284', '0.7617', '0.06137', '-0.3838', '0.2788', '-0.001342', '-0.1682', '0.3433', '0.3323', '-0.46', '0.03', '0.3271', '0.6357', '-0.1471', '0.526', '-0.3018', '-0.3433', '0.05988', '-0.4924', '0.898', '0.557', '-0.356', '0.0859', '-0.1233', '-0.2803', '0.00397', '-0.206', '0.3655', '0.852', '-0.1159', '-0.0002043', '0.1221', '0.02985', '0.03485', '-0.0886', '0.504', '-0.04733', '0.1133', '0.3313', '0.7783', '0.3372', '0.534', '0.0138', '-0.3022', '-0.0773']",,,,,,,
mondo:0015089,autosomal recessive complex spastic paraplegia,"['autosomal recessive complex HSP', 'autosomal recessive complex SPG', 'autosomal recessive complex hereditary spastic paraplegia', 'complex hereditary spastic paraplegia, autosomal recessive', 'autosomal recessive complicated HSP', 'autosomal recessive complicated SPG', 'autosomal recessive complicated spastic paraplegia']",,,100981,CN228909,"['-0.05518', '0.2744', '-0.1493', '-0.1508', '-0.2301', '-0.6187', '-0.358', '-0.001088', '-0.2908', '-0.3477', '-0.003115', '-0.1456', '0.01507', '0.3757', '0.7407', '0.10504', '-0.3816', '-0.282', '0.2004', '-0.3892', '0.1313', '-0.1764', '0.2637', '0.2678', '0.02815', '-0.02345', '0.2195', '-0.02132', '-0.1194', '-0.285', '0.2693', '0.1677', '0.1067', '0.2996', '0.0739', '-0.308', '-0.0922', '-0.3372', '-0.1882', '-0.2291', '-0.03513', '-0.677', '-0.1175', '0.2126', '-0.02415', '-0.4856', '-0.312', '0.2573', '-0.015045', '0.1493', '-0.0662', '-0.02785', '-0.2595', '-0.1301', '0.0389', '-0.6333', '0.6465', '0.04337', '-0.4004', '0.3054', '-0.0147', '-0.152', '0.4387', '0.316', '-0.4338', '0.03586', '0.331', '0.6167', '-0.1265', '0.5757', '-0.2593', '-0.278', '0.1437', '-0.443', '0.866', '0.5664', '-0.3525', '0.0924', '-0.1289', '-0.186', '0.009056', '-0.1289', '0.4038', '0.85', '-0.08704', '-0.01654', '0.1624', '0.02231', '0.05472', '-0.09326', '0.4749', '0.03497', '0.06836', '0.3318', '0.775', '0.3035', '0.46', '-0.01762', '-0.2202', '-0.073']",,,,,,,
mondo:0015090,autosomal recessive pure spastic paraplegia,"['pure hereditary spastic paraplegia, autosomal recessive', 'autosomal recessive pure hereditary spastic paraplegia', 'autosomal recessive pure HSP', 'autosomal recessive uncomplicated spastic paraplegia', 'autosomal recessive pure SPG', 'autosomal recessive uncomplicated HSP', 'autosomal recessive uncomplicated SPG']",,,100982,CN228910,"['-0.01733', '0.2059', '-0.12366', '-0.1692', '-0.1776', '-0.621', '-0.3499', '-0.002836', '-0.283', '-0.4106', '-0.01359', '-0.12256', '0.015396', '0.42', '0.6943', '0.1614', '-0.3074', '-0.2428', '0.1892', '-0.4365', '0.135', '-0.2134', '0.2345', '0.1833', '0.00985', '-0.00848', '0.1624', '-0.05054', '-0.05707', '-0.2795', '0.3083', '0.1844', '0.05984', '0.2458', '0.0626', '-0.3545', '-0.11865', '-0.3625', '-0.11633', '-0.2761', '-0.0478', '-0.6304', '-0.0982', '0.2394', '-0.03918', '-0.45', '-0.2668', '0.2976', '0.04303', '0.08563', '-0.03268', '-0.0424', '-0.2428', '-0.1326', '0.0745', '-0.618', '0.697', '0.0785', '-0.3635', '0.3125', '0.01474', '-0.1362', '0.3901', '0.2477', '-0.4236', '0.0339', '0.2832', '0.598', '-0.1646', '0.514', '-0.2896', '-0.2666', '0.0975', '-0.4858', '0.754', '0.5664', '-0.36', '0.09467', '-0.10974', '-0.2098', '-0.003765', '-0.1741', '0.3926', '0.8457', '-0.1349', '0.03168', '0.134', '0.00896', '0.05582', '-0.05258', '0.466', '0.05908', '0.09155', '0.3083', '0.785', '0.3318', '0.4807', '-0.02466', '-0.2374', '-0.05014']",,,,,,,
mondo:0015091,autosomal dominant spastic paraplegia type 9,"['ALDH18A1 autosomal dominant complex spastic paraplegia', 'spastic paraplegia 9', 'autosomal dominant spastic paraparesis', 'cataracts-motor neuropathy-short stature-skeletal anomalies syndrome', 'spastic paraparesis-amyopathy-cataracts-gastroesophageal reflux syndrome', 'SPG9', 'cataracts, motor neuronopathy, short stature and skeletal abnormalities', 'autosomal dominant complex spastic paraplegia caused by mutation in ALDH18A1', 'bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy']",,,100990,,"['-0.07874', '0.2295', '-0.1378', '-0.145', '-0.209', '-0.7515', '-0.3481', '-0.002096', '-0.4275', '-0.4377', '-0.01238', '-0.1648', '-0.05484', '0.4167', '0.802', '0.0491', '-0.3586', '-0.2225', '0.1656', '-0.3875', '0.2332', '-0.2217', '0.225', '0.1842', '0.0968', '-0.004143', '0.2095', '0.02824', '-0.1207', '-0.2395', '0.2908', '0.1466', '0.05563', '0.2925', '0.1704', '-0.4417', '-0.0247', '-0.2566', '-0.1428', '-0.2673', '0.01723', '-0.604', '-0.05115', '0.3047', '-0.0984', '-0.514', '-0.2646', '0.2651', '0.0752', '0.0497', '-0.01846', '-0.07666', '-0.254', '-0.1475', '-0.01775', '-0.649', '0.7183', '0.09467', '-0.353', '0.3037', '-0.1255', '-0.0975', '0.4578', '0.2703', '-0.4092', '0.1407', '0.246', '0.4937', '-0.1685', '0.506', '-0.3062', '-0.2878', '0.1307', '-0.4753', '0.817', '0.4436', '-0.3643', '0.1354', '-0.1113', '-0.1173', '-0.0414', '-0.1603', '0.3896', '0.7524', '-0.12085', '-0.1136', '0.1995', '0.1501', '0.10046', '-0.02586', '0.412', '-0.04504', '0.138', '0.2058', '0.7983', '0.3037', '0.4648', '-0.0719', '-0.2089', '-0.1065']",,,,,,,
mondo:0015092,cleft hard palate,,,,101023,,,,,,,Q35.1,,
mondo:0015093,sub-cortical nodular heterotopia,,,,101029,,,,,,,,,
mondo:0015094,subependymal nodular heterotopia,,,,101030,C3160906,,,,,742.4,,10071150,
mondo:0015095,Peters anomaly-cataract syndrome,,,,101033,C2931652,,,,C537885,,,,
mondo:0015096,familial hypofibrinogenemia,"['hypofibrinogenemia, familial']",,,101041,CN197419,"['-0.4224', '-0.0929', '-0.2908', '-0.1022', '-0.1069', '0.0926', '0.1766', '0.3308', '-0.11285', '0.08215', '0.05374', '-0.0593', '-0.1383', '0.0913', '-0.00991', '0.02078', '0.1069', '-0.000807', '-0.08704', '-0.4036', '-0.2091', '0.04083', '0.4058', '-0.0743', '-0.04025', '0.014404', '0.095', '-0.10144', '-0.093', '0.0653', '0.0883', '-0.0168', '0.1637', '0.1635', '-0.1757', '-0.1345', '-0.04752', '-0.3354', '0.1095', '-0.0806', '0.2211', '-0.1196', '0.12103', '-0.2267', '0.151', '-0.06445', '-0.09436', '0.0963', '0.0069', '0.05984', '0.2396', '-0.256', '0.1058', '-0.0914', '-0.3433', '0.2245', '0.33', '-0.3022', '-0.3228', '0.005154', '-0.02469', '0.1971', '0.2788', '-0.2705', '0.1868', '0.1359', '0.2605', '0.1156', '-0.5083', '0.2206', '-0.1573', '0.0328', '-0.1693', '-0.3418', '0.3293', '0.372', '0.3613', '0.09393', '0.0464', '-0.2001', '-0.03433', '0.02547', '-0.09216', '0.1238', '0.1777', '0.2274', '0.1079', '0.2544', '0.4263', '-0.3022', '0.222', '0.2615', '-0.02437', '-0.09656', '0.4214', '0.1273', '0.26', '-0.4233', '-0.3208', '0.2607']",,,,,,,
mondo:0015097,aortic valve dysplasia,,,,101043,,,,,,746.89,,,
mondo:0015099,unilateral hemispheric polymicrogyria,,,,101071,,,,,,,,,
mondo:0015100,aregenerative anemia,,,,101096,C0553669,,,,,,,10054329,
mondo:0015101,Marin-Amat syndrome,,,,101104,CN197448,,,,,,,,
mondo:0015102,non-secreting chemodectoma,,,,101106,,,,,,,,,
mondo:0015103,pulmonary valve agenesis-tetralogy of fallot-absence of ductus arteriosus syndrome,"['PVA/ADA, Fallot type', 'APV/ADA, Fallot type', 'absence of pulmonary valve-Fallot tetralogy-absence of ductus arteriosus syndrome']",,,101206,CN197455,,,,,,,,
mondo:0015104,porphyria cutanea tarda,"['PCT', 'porphyria cutania tarda']",3132,,101330,C0162566,"['0.1538', '-0.0261', '-0.792', '-0.4753', '0.08234', '-0.3225', '0.1519', '-0.0655', '-0.562', '0.03818', '-0.04968', '0.4856', '-0.157', '1.017', '-0.859', '-0.1836', '0.2656', '0.2124', '-0.2307', '-0.4724', '-0.5527', '-0.255', '0.4597', '-0.1306', '0.04486', '-0.4648', '0.04907', '-0.1938', '0.536', '-0.8433', '0.2277', '-0.5874', '0.6235', '-0.946', '-0.4998', '-0.2634', '-0.7363', '-0.1272', '0.05594', '-0.2803', '0.2272', '-0.3713', '0.1746', '-0.2236', '0.1148', '-0.5376', '0.26', '-0.373', '0.748', '0.03143', '-0.12006', '0.636', '0.9624', '0.1605', '-0.004498', '-0.02779', '-0.06207', '0.0732', '-0.424', '-0.4878', '0.04257', '-0.1245', '1.057', '-0.2258', '-0.137', '0.3997', '0.01659', '0.805', '0.4749', '0.1917', '-0.4307', '-0.2605', '0.301', '-0.7173', '0.3782', '0.516', '0.523', '-0.07794', '0.1653', '-0.532', '0.3333', '-0.7266', '0.05023', '-0.8623', '0.6978', '0.2554', '0.967', '0.4429', '-0.08765', '0.08997', '0.736', '-0.1522', '-0.5176', '0.35', '0.2883', '0.5376', '0.08453', '-0.6475', '0.0225', '0.1395']",C27725,,D017119,,,10036183,
mondo:0015109,congenital anomaly of the mitral subvalvular apparatus,,,,101932,,,,,,,,,
mondo:0015111,gastroesophageal disease,,,,101936,CN197468,,,,,,,,
mondo:0015126,polyendocrinopathy,,,,101956,,,,,,,,,
mondo:0015127,pituitary deficiency,,,,101957,C0020635,,,,,,E23.0,,
mondo:0015128,primary adrenal insufficiency,,,,101958,C3887896,,C113172,,,,,10052381,
mondo:0015129,chronic primary adrenal insufficiency,"['classic Addison^s disease', 'Addison disease, chronic adrenal insufficiency', 'primary adrenal insufficiency, chronic', 'Addison^s disease', 'hypoadrenocorticism familial', 'adrenal hypoplasia', 'CPAI', 'adrenal aplasia', 'autoimmune primary adrenal insufficiency', 'primary hypoadrenalism', 'primary adrenocortical insufficiency', 'autoimmune Addison disease', 'chronic adrenocorticoid insufficiency', 'adrenal gland hypofunction', 'autoimmune adrenalitis', 'Addison disease', 'hypoadrenocorticism, familial', 'primary Addison^s disease']",13774,240200,101959,C0271737,,C26689,,D000224,255.41,,10001130,
mondo:0015130,acquired chronic primary adrenal insufficiency,['acquired chronic primary adrenal insufficiency'],,,101963,,,,,,,,,
mondo:0015131,combined immunodeficiency,"['CID', 'congenital combined immunodeficiency', 'combined immunodeficiency', 'X-linked combined immunodeficiency', 'combined T and B cell immunodeficiency', 'combined T cell and B cell immunodeficiency']",628,,101972,C0494261,,C27871,,,279.2,,,
mondo:0015132,immunodeficiency predominantly affecting antibody production,,,,101977,,,,,,,,,
mondo:0015133,quantitative and/or qualitative congenital phagocyte defect,,,,101985,,,,,,,,,
mondo:0015134,constitutional neutropenia,"['Kostmann disease', 'Kostmann neutropenia', 'genetic infantile agranulocytosis', 'Kostmann syndrome', 'infantile genetic agranulocytosis', 'congenital neutropenia']",,,101987,,,C61242,,,,D70,,
mondo:0015135,primary immunodeficiency due to a genetic defect in innate immunity,['primary immunodeficiency due to a defect in innate immunity'],,,101988,,,,,,,,,
mondo:0015137,periodic fever syndrome,,,,101995,C3889979,,C118240,,,,,10034533,
mondo:0015140,early-onset autosomal dominant Alzheimer disease,"['EOFAD', 'early-onset, autosomal dominant Alzheimer disease', 'early-onset familial autosomal dominant Alzheimer disease']",,,1020,CN043596,"['0.266', '0.292', '-0.251', '-0.10645', '-0.2102', '-0.294', '-0.159', '0.3215', '-0.803', '-0.1141', '-0.1895', '-0.4832', '-0.1043', '-0.1353', '0.8325', '-0.5625', '-0.382', '0.1604', '0.1417', '-0.4058', '0.0832', '-0.2588', '-0.02144', '-0.0841', '0.2245', '0.04907', '-0.2227', '-0.3735', '-0.0728', '0.007965', '0.583', '0.11', '0.3894', '0.11163', '0.1758', '-0.0649', '-0.3596', '-0.2563', '-0.2273', '-0.2029', '0.614', '-0.484', '0.552', '-0.003187', '0.4285', '-0.362', '-0.2435', '-0.1829', '-0.1694', '-0.04785', '0.2795', '0.751', '-0.0837', '-0.2122', '0.398', '0.1625', '0.522', '-0.2123', '-0.5303', '0.12036', '0.08044', '0.388', '0.6763', '0.01357', '-0.04364', '0.02397', '0.1523', '0.1619', '0.1997', '0.4968', '0.0624', '-0.07104', '-0.0539', '-0.2085', '0.861', '0.1655', '-0.3008', '-0.1354', '-0.2377', '-0.521', '0.0904', '-0.0837', '0.059', '0.4192', '0.05804', '0.4111', '0.1876', '0.3179', '0.1813', '0.1008', '0.09216', '0.2688', '-0.05978', '-0.1364', '0.1389', '0.3828', '0.1522', '-0.3435', '-0.4084', '0.0318']",,,,,,,
mondo:0015141,disorder of medulla oblongata,"['disorder of medulla oblongata', 'disease of medulla oblongata', 'medullar disease', 'medulla oblongata disease or disorder', 'medulla oblongata disease']",,,102000,CN197487,,,,,,,,
mondo:0015144,brain inflammatory disease,['brain inflammation'],,,102005,CN197488,,,,,,,,
mondo:0015145,neurovascular malformation,,,,102006,,,,,,,,,
mondo:0015146,classic lissencephaly,"['lissencephaly sequence isolated', 'lissencephaly classic', 'lissencephaly type 1', 'ILS']",,,102009,,,,,,,,,
mondo:0015148,lissencephaly type 3,,0112232,,102011,,,,,,,,,
mondo:0015149,pure hereditary spastic paraplegia,"['uncomplicated hereditary spastic paraplegia', 'uncomplicated SPG', 'Pure HSP', 'uncomplicated familial spastic paraplegia', 'Pure SPG', 'uncomplicated HSP', 'Pure familial spastic paraplegia']",,,102012,C0393555,,,,,,,,
mondo:0015150,complex hereditary spastic paraplegia,"['Complex HSP', 'Complex SPG', 'complicated hereditary spastic paraplegia', 'syndromic hereditary spastic paraplegia', 'complicated HSP', 'complicated SPG', 'syndrome associated with hereditary spastic paraplegia', 'complicated familial spastic paraplegia', 'Complex familial spastic paraplegia']",,,102013,CN197491,,,,,,,,
mondo:0015151,"muscular dystrophy, limb-girdle, autosomal dominant","['autosomal dominant limb-girdle muscular dystrophy', 'limb-girdle muscular dystrophy, autosomal dominant', 'muscular dystrophy, limb-girdle, autosomal dominant']",0110273,,102014,CN228919,,,,,,,,
mondo:0015152,autosomal recessive limb-girdle muscular dystrophy,"['limb-girdle muscular dystrophy, autosomal recessive', 'muscular dystrophy, limb-girdle, autosomal recessive']",0110274,,102015,C2931907,"['-0.2294', '-0.7896', '-0.39', '-0.3496', '0.677', '-1.354', '0.0674', '0.512', '-1.883', '-0.9927', '0.000689', '0.4138', '-0.2576', '0.985', '0.292', '0.2351', '-0.8203', '-0.65', '-0.515', '-1.119', '-0.2136', '0.3364', '0.3096', '0.703', '0.2766', '-0.1819', '-0.1477', '-1.123', '0.2294', '-0.557', '0.834', '-0.044', '0.6484', '0.1873', '0.3137', '0.1348', '-0.6704', '0.3325', '0.1757', '-0.6245', '0.222', '-0.2051', '-0.4023', '0.409', '-0.02649', '0.405', '0.11017', '0.8325', '-0.1643', '0.5464', '0.5894', '-0.3657', '0.3093', '-0.682', '0.16', '-0.71', '0.377', '1.162', '-0.2646', '0.002579', '-0.10693', '-0.08405', '0.01752', '-0.07007', '-0.099', '0.03333', '0.06354', '0.5537', '-0.332', '-0.2355', '-0.06354', '0.4778', '0.2484', '-0.3503', '0.7', '0.4614', '-0.2439', '0.4539', '-0.06775', '0.08887', '0.2059', '0.008705', '-0.2932', '0.1707', '-0.1741', '0.1433', '-0.1759', '-0.527', '0.9116', '0.4072', '-0.442', '0.092', '0.5234', '0.911', '-0.1425', '0.1819', '0.157', '-0.4841', '-0.2401', '-0.1013']",,,C538640,,,,
mondo:0015157,human herpesvirus 8-related tumor,['HHV-8-related disorder'],,,102024,CN226610,,,,,,,,
mondo:0015158,unexplained periodic fever syndrome,,,,102237,CN197498,,,,,,,,
mondo:0015159,multiple congenital anomalies/dysmorphic syndrome-intellectual disability,"['multiple congenital anomalies-intellectual disability with or without dysmorphism', 'MCA/MR']",,,102283,CN228396,"['-0.0975', '0.03955', '0.08093', '-0.05563', '0.076', '-0.1461', '0.05267', '0.163', '-0.132', '-0.0962', '0.02043', '0.02203', '0.04855', '-0.03397', '-0.03732', '-0.06995', '-0.0502', '-0.0076', '-0.0769', '-0.2766', '0.03275', '0.0391', '0.0744', '-0.07324', '0.0845', '-0.05582', '-0.06757', '-0.04846', '0.0502', '-0.0862', '0.103', '0.04138', '0.1781', '0.1145', '0.0672', '-0.08813', '-0.0738', '-0.10455', '-0.0778', '-0.09045', '0.0893', '-0.11816', '0.02072', '-0.04587', '0.0327', '-0.1719', '-0.01663', '0.1306', '0.01522', '0.01985', '-0.11847', '0.0117', '0.05286', '-0.03119', '-0.1198', '-0.02957', '0.0763', '-0.0336', '-0.0905', '-0.004528', '0.11176', '0.03696', '0.02882', '0.03348', '-0.0351', '0.01275', '0.134', '0.1187', '-0.1532', '0.0916', '-0.10736', '0.03644', '-0.00612', '-0.08826', '0.02167', '-0.00803', '0.0751', '-0.02855', '-0.136', '0.0004992', '-0.008484', '0.0845', '-0.0936', '0.1454', '-0.00522', '-0.02124', '0.0294', '0.125', '0.08875', '0.11176', '0.04413', '0.1931', '0.06213', '0.02687', '0.2329', '0.05145', '0.175', '-0.1528', '0.09717', '0.0886']",,,,,,,
mondo:0015160,multiple congenital anomalies/dysmorphic syndrome-variable intellectual disability syndrome,"['multiple congenital anomalies-variable intellectual disability with or without dysmorphism syndrome', 'MCA/variable MR']",,,102284,,,,,,,,,
mondo:0015161,multiple congenital anomalies/dysmorphic syndrome without intellectual disability,"['multiple congenital anomalies without intellectual disability with or without dysmorphism', 'MCA without intellectual disability']",,,102285,,,,,,,,,
mondo:0015164,acute myeloid leukemia and myelodysplastic syndromes related to alkylating agent,['AML and myelodysplastic syndromes related to alkylating agent'],,,102379,CN197504,,,,,,,,
mondo:0015165,acute myeloid leukemia and myelodysplastic syndromes related to topoisomerase type 2 inhibitor,['AML and myelodysplastic syndromes related to topoisomerase type 2 inhibitor'],,,102381,CN197505,,,,,,,,
mondo:0015166,acute myeloid leukemia with t(8;21)(q22;q22) translocation,['AML with t(8;21)(q22;q22) translocation'],,,102724,,,,,,,,,
mondo:0015167,amniotic band syndrome,"['Streeter dysplasia', 'congenital ring constrictions', 'amputation, congenital', 'Adam syndrome', 'amniotic band sequence', 'congenital constricting bands', 'constriction band syndrome', 'familial amniotic bands', 'terminal transverse defects of arm', 'Adam Complex', 'amniotic band constriction', 'CONSTRICTING bands, congenital', 'Streeter anomaly', 'constriction rings syndrome', 'amniotic bands sequence', 'deformity due to amniotic band', 'amniotic deformity-adhesion-mutilation syndrome']",,217100,295000,,,C84552,,D000652,,,,
mondo:0015168,arthrogryposis multiplex congenita,"['Guerin-Stern syndrome', 'Rossi syndrome', 'congenital amyoplasia', 'myodysplasia', 'Otto syndrome', 'fibrous ankylosis of multiple joints', 'Arthromyodysplasia congenita', 'multiple congenital arthrogryposis', 'amyoplasia congenita', 'AMC', 'rocher-Sheldon syndrome', 'congenital arthromyodysplasia', 'myodystrophia fetalis deformans', 'Guérin-Stern syndrome']",0080954,,1037,,,,,,,,10051643,
mondo:0015169,chronic diarrhea due to glucoamylase deficiency,['maltase-glucoamylase deficiency'],,,103907,C4275068,,,,,,,,
mondo:0015170,congenital sodium diarrhea,['Na-H exchange deficiency'],,,103908,,"['0.2417', '0.0952', '0.4048', '0.10864', '-0.2705', '-0.2598', '-0.9766', '0.4949', '-0.10455', '0.0309', '0.688', '0.522', '0.3438', '0.6006', '-0.942', '0.0214', '-0.332', '-0.03029', '-0.6836', '-0.8794', '0.2551', '-0.02022', '-0.2177', '0.0806', '0.355', '-0.513', '-0.7856', '0.5156', '0.2966', '-0.957', '-0.1699', '-0.5015', '0.0555', '0.3645', '0.8374', '0.598', '-0.428', '0.4553', '0.1947', '0.2457', '-0.4739', '-0.4502', '-0.4126', '-0.7305', '0.289', '0.03964', '-0.08295', '0.3633', '-0.3228', '1.049', '-1.006', '-0.3965', '-0.04202', '-0.723', '-0.0423', '-0.1777', '-0.1235', '-0.189', '-0.664', '-0.1888', '0.925', '0.3303', '0.3857', '-0.5586', '-0.03143', '-0.3936', '0.416', '-0.2125', '0.10364', '0.97', '-0.1633', '0.577', '0.1691', '-0.82', '0.551', '0.342', '-0.4023', '0.1081', '-0.00767', '0.653', '-0.05334', '-0.7163', '0.04144', '0.1364', '0.226', '0.5586', '0.5205', '0.1488', '0.0377', '-0.0641', '0.1137', '-0.3271', '-0.49', '-0.5425', '0.4182', '0.612', '0.3132', '-1.513', '-0.1536', '-0.3613']",,,,,,,
mondo:0015171,congenital enterocyte heparan sulfate deficiency,,,,103910,,,,,,,,,
mondo:0015174,autoimmune enteropathy type 3,,,,103917,CN226617,,,,,,,,
mondo:0015175,autoimmune pancreatitis,"['AIP', 'lymphoplasmocytic sclerosing pancreatitis']",0040091,,103919,C2609129,,,,D000081012,,,10069002,
mondo:0015176,undetermined colitis,,,,103920,,,,,,,K52.3,,
mondo:0015177,metaphyseal anadysplasia,"['MAD', 'early-onset regressive form of metaphyseal dysplasia', 'regressive metaphyseal dysplasia', 'Maroteaux-Verloes-Stanescu syndrome', 'Maroteaux Verloes Stanescu syndrome']",,309645,1040,C0432226,"['-0.2462', '0.252', '0.00576', '-0.07965', '0.143', '-0.814', '-0.1149', '0.387', '-0.3767', '-0.557', '-0.3904', '0.49', '-0.1467', '0.3257', '0.2136', '0.3572', '0.1742', '-0.0555', '-0.02003', '-0.2389', '-0.3508', '0.2067', '0.4841', '-0.3242', '0.4204', '0.3386', '0.1613', '-0.02922', '-0.0721', '0.2551', '0.2532', '-0.4277', '0.01218', '0.1312', '0.2822', '0.3484', '-0.5347', '-0.4343', '-0.2876', '-0.03168', '0.3093', '-0.509', '0.02338', '0.0999', '-0.03214', '-0.373', '-0.8975', '0.4294', '0.0855', '-0.001223', '0.325', '0.0462', '0.0561', '-0.002102', '-0.5713', '-0.9136', '-0.1958', '0.0409', '-0.1041', '0.08594', '0.4583', '-0.2524', '-0.5835', '0.1523', '-0.338', '-0.1912', '0.182', '0.3726', '-0.1118', '0.545', '0.205', '-0.02023', '0.707', '0.1353', '0.3367', '0.4097', '-0.1802', '0.1631', '-0.0648', '-0.3057', '-0.2356', '-0.362', '0.1833', '-0.1788', '0.02145', '0.4846', '-0.1', '0.4558', '0.41', '0.2002', '-0.183', '0.6626', '0.04816', '0.3386', '0.3372', '0.587', '0.971', '-0.7773', '0.1368', '-0.0516']",,,C537351,756.9,,,
mondo:0015178,congenital intestinal transport defect,,,,104003,,,,,,,,,
mondo:0015179,intestinal disease due to vitamin absorption anomaly,,,,104004,CN197521,,,,,,,,
mondo:0015180,intestinal disease due to fat malabsorption,,,,104005,CN197522,,,,,,,,
mondo:0015182,congenital enteropathy involving intestinal mucosa development,,,,104007,,,,,,,,,
mondo:0015183,short bowel syndrome,"['short gut syndrome', 'acquired short bowel syndrome']",10605,,104008,C0036992,,C99059,,D012778,579.3,,10049416,
mondo:0015185,intestinal polyposis syndrome,,,,104010,CN197525,,C155954,,,,,10057018,
mondo:0015191,myopathic intestinal pseudoobstruction,,,,104077,,,,,,,,,
mondo:0015193,hydrops fetalis,"['hydrops fetalis nonimmune', 'hydrops fetalis', 'fetal hydrops', 'hydrops fetalis (disease)', 'fetal anasarca', 'foetal anasarca', 'HF', 'foetal hydrops', 'idiopathic hydrops fetalis', 'generalized fetal edema', 'foetal oedema', 'familial non-immune hydrops fetalis', 'fetal edema', 'generalised foetal oedema']",,,1041,C0020305,,C84767,,D015160,,,10020529,0001789
mondo:0015194,sideroblastic anemia,"['sideroblastic anemia', 'anemia, hypochromic with iron loading', 'anaemia sideroblastic', 'anemia sideroblastic']",8955,,1047,C0002896,,C36078,,D000756,285.0,,10040661,
mondo:0015195,atresia of urethra,"['atresia of urethra (disease)', 'urethral atresia', 'atresia of urethra']",,,105,,,,,,,Q64.3,10064895,0000068
mondo:0015196,vein of Galen aneurysm,"['Galen vein aneurysm', 'ectasia or varix of the vein of Galen', 'Galenic arteriovenous malformation', 'vein of Galen aneurysm malformation', 'vein of Galen arteriovenous malformations', 'VGAM']",,,1053,C0431420,,,,C536535,,,,
mondo:0015197,aneurysm of sinus of Valsalva,"['SVA', 'sinus of Valsalva aneurysm']",,,1054,CN197542,,,,,747.29,,,
mondo:0015198,aniridia-ptosis-intellectual disability-familial obesity syndrome,['aniridia - ptosis - intellectual disability - familial obesity'],,,1067,CN226622,,,,,,,,
mondo:0015199,aniridia - intellectual disability syndrome,"['Walker-Dyson syndrome', 'aniridia associated with mental retardation and other eye abnormalities', 'Walker Dyson syndrome', 'aniridia associated with intellectual disability and other eye abnormalities']",,,1068,C2931243,,,,C536568,,,,
mondo:0015200,anisakiasis,"['infections, Anisakis simplex', 'infection by Anisakis larva', 'Anisakis infection', 'Anisakis simplex infection', 'Pseudoterranova infection', 'Anisakiases']",7033,,1070,C0162576,,C128393,0007146,D017129,127.1,B81.0,10002533,
mondo:0015201,ankyloblepharon filiforme-imperforate anus syndrome,"['ankyloblepharon filiforme adnatum-imperforate anus syndrome', 'Aughton-Hufnagle syndrome']",,,1074,CN197555,,,,,,,,
mondo:0015203,coronary artery congenital malformation,,,,1081,,,,,,,,10061060,
mondo:0015204,microlissencephaly,,0112234,,1083,C1956147,"['-0.3877', '0.2448', '0.2416', '-0.0876', '0.2194', '-0.0914', '0.2216', '0.0335', '-0.352', '-0.2006', '-0.4062', '-0.2373', '-0.004215', '-0.3', '0.1595', '-0.0796', '0.0922', '-0.3286', '-0.001164', '-0.5186', '0.10803', '-0.0737', '0.4094', '-0.147', '0.2184', '-0.2372', '-0.04636', '0.01281', '-0.407', '0.17', '0.2482', '0.10846', '0.4937', '0.1392', '0.02524', '0.2172', '-0.5073', '-0.05963', '-0.3484', '-0.3389', '0.17', '-0.4902', '-0.1214', '-0.0945', '-0.2979', '-0.09644', '-0.1678', '-0.03014', '0.1498', '-0.03104', '0.0672', '-0.00899', '-0.1027', '0.1265', '-0.1306', '-0.1348', '0.21', '0.08264', '-0.1758', '0.3003', '-0.131', '-0.08276', '0.02548', '0.0454', '-0.252', '-0.013664', '0.3403', '0.2242', '-0.3274', '0.3733', '0.03082', '0.1262', '0.425', '0.2448', '-0.0264', '-0.1726', '0.253', '-0.0877', '-0.4448', '-0.2874', '-0.3215', '0.000714', '-0.1798', '0.2932', '0.10767', '-0.263', '-0.1158', '0.3245', '0.01166', '-0.1121', '0.2211', '0.2457', '-0.2231', '0.2505', '0.3271', '0.1715', '0.3997', '-0.1508', '0.306', '0.3123']",,,,,,,
mondo:0015205,isolated lissencephaly type 1 without known genetic defects,,,,1084,CN226623,,,,,,,,
mondo:0015206,short stature-heart defect-craniofacial anomalies syndrome,"['Rommen Mueller Sybert syndrome', 'Rommen-Mueller-Sybert syndrome', 'short stature heart defect and craniofacial anomalies']",,,1088,C2931050,,,,C535871,,,,
mondo:0015207,non-syndromic esophageal malformation,"['nonsyndromic esophageal malformation', 'isolated esophageal malformation']",,,108959,,,,,,,,,
mondo:0015208,syndromic esophageal malformation,"['syndromic esophageal malformation', 'syndrome associated with esophageal malformation']",,,108961,CN226625,,,,,,,,
mondo:0015209,non-syndromic gastroduodenal malformation,"['nonsyndromic gastroduodenal malformation', 'isolated gastroduodenal malformation']",,,108963,,,,,,,,,
mondo:0015210,syndromic gastroduodenal malformation,"['syndrome associated with gastroduodenal malformation', 'syndromic gastroduodenal malformation']",,,108965,CN226627,,,,,,,,
mondo:0015211,non-syndromic intestinal malformation,"['isolated intestinal malformation', 'nonsyndromic intestinal malformation']",,,108967,,,,,,,,,
mondo:0015212,syndromic intestinal malformation,"['syndromic intestinal malformation', 'syndrome associated with intestinal malformation']",,,108969,CN226629,,,,,,,,
mondo:0015213,non-syndromic visceral malformation,"['isolated visceral malformation', 'nonsyndromic visceral malformation']",,,108971,,,,,,,,,
mondo:0015214,syndromic visceral malformation,,,,108973,CN226631,,,,,,,,
mondo:0015217,non-syndromic developmental defect of the eye,"['nonsyndromic developmental defect of the eye', 'isolated developmental defect of the eye']",,,108985,,,,,,,,,
mondo:0015219,non-syndromic central nervous system malformation,"['isolated central nervous system malformation', 'nonsyndromic central nervous system malformation']",,,108989,,,,,,,,,
mondo:0015221,non-syndromic respiratory or mediastinal malformation,"['isolated respiratory or mediastinal malformation', 'nonsyndromic respiratory or mediastinal malformation']",,,108993,,,,,,,,,
mondo:0015222,syndromic respiratory or mediastinal malformation,"['syndromic respiratory or mediastinal malformation', 'syndrome associated with respiratory or mediastinal malformation']",,,108995,CN226638,,,,,,,,
mondo:0015225,arthrogryposis syndrome,,,,109007,C0003886,,,,D001176,,,,
mondo:0015227,non-syndromic limb malformation,"['nonsyndromic limb malformation', 'isolated limb malformation']",,,109011,,,,,,,,,
mondo:0015228,pentasomy X,"['penta-X syndrome', '49, XXXXX syndrome', '49,XXXXX syndrome', 'Pentasomy type X', 'poly-X', 'XXXXX syndrome', 'Pentasomy X syndrome', 'chromosome XXXXX syndrome', 'chromosome X pentasomy', 'penta-X', 'penta X syndrome']",,,11,C0265497,,C89802,,C535319,,,,
mondo:0015229,Bardet-Biedl syndrome,['BBS'],1935,,110,C0752166,"['0.2688', '-0.0916', '0.1643', '0.04572', '-0.2024', '-0.566', '-0.447', '0.6504', '-0.766', '-0.2893', '-0.5347', '-0.475', '0.1952', '0.2407', '0.1356', '-0.253', '-0.05576', '0.02725', '-0.1771', '-1.236', '0.08905', '-0.05914', '0.5684', '-0.4543', '0.1821', '0.0895', '-0.3481', '-0.05603', '0.688', '-0.35', '0.523', '0.03882', '0.392', '0.2512', '0.4023', '-0.0926', '-0.0801', '-0.03632', '-0.7095', '0.2396', '0.2854', '0.0821', '0.1604', '-0.09467', '0.5737', '-0.08606', '0.3809', '-0.2458', '-0.351', '-0.5063', '-0.218', '0.754', '-0.0842', '-0.1632', '0.4888', '-0.348', '0.3', '-0.261', '-0.509', '0.0728', '0.04437', '-0.2167', '0.5024', '0.1227', '0.002035', '0.001163', '0.2386', '0.643', '-0.663', '0.311', '-0.6665', '0.403', '0.352', '0.1316', '0.3848', '-0.443', '-0.2345', '-0.01493', '0.006714', '-0.1175', '0.1772', '0.2368', '-0.4792', '-0.01656', '-0.02472', '0.1862', '0.7407', '-0.1367', '0.1653', '0.145', '0.2566', '0.04468', '0.3926', '0.2351', '0.4949', '-0.71', '-0.4158', '-0.2622', '0.1081', '-0.1827']",C118632,,D020788,759.89,,10056715,
mondo:0015230,anophthalmia-megalocornea-cardiopathy-skeletal anomalies syndrome,"['anophthalmia megalocornea cardiopathy skeletal anomalies', 'Cassia Stocco dos Santos syndrome']",,,1101,CN197570,,,,,,,,
mondo:0015231,Bartter syndrome,"['hypokalemic alkalosis', 'salt-losing tubular disorder, Henle^s loop type', 'Bartter disease', 'aldosteronism with hyperplasia of the adrenal cortex', 'Bartter^s syndrome', 'salt-wasting tubulopathy, Henle^s loop type', 'Potassium wasting', 'renal tubular normotensive hypokalemic alkalosis with hypercalciuria', 'hypokalemic alkalosis with hypercalciuria']",445,,112,C0085570,,C34412,,D001477,255.13,,10050839,
mondo:0015232,radial deficiency-tibial hypoplasia syndrome,,,,1121,CN226642,,,,,,,,
mondo:0015233,caudal appendage-deafness syndrome,"['caudal appendage, short terminal phalanges, deafness, cryptorchidism and mental retardation', 'caudal appendage deafness', 'Lynch Lee Murday syndrome', 'Lynch-Lee-Murday syndrome', 'caudal appendage, short terminal phalanges, deafness, cryptorchidism and intellectual disability']",,,1123,C2931593,,,,C537713,,,,
mondo:0015234,arachnodactyly-abnormal ossification-intellectual disability syndrome,"['arachnodactyly, abnormal ossification and intellectual disability', 'arachnodactyly, abnormal ossification and mental retardation', 'Kosztolanyi syndrome']",,,1129,C2931398,,,,C537024,,,,
mondo:0015235,arachnodactyly-intellectual disability-dysmorphism syndrome,"['arachnodactyly - intellectual disability - dysmorphism', 'De Die-Smulders-Vles-Fryns syndrome']",,,1130,CN197590,,,,,,,,
mondo:0015236,aortic arch defects,,,,1132,,,,,,,,,
mondo:0015237,arrhinia,"['Nose agenesis', 'isolated nose agenesis', 'isolated arrhinia', 'congenital absence of the nose', 'Nose agenesia']",,,1134,,,,,C537438,748.1,,,
mondo:0015238,arrhinia-choanal atresia-microphthalmia syndrome,"['arhinia choanal atresia microphthalmia', 'Bosma arhinia microphthalmia syndrome', 'Bosma Henkin Christiansen syndrome', 'congenital absence of nose and anterior nasopharynx']",,,1135,,,,,,,,,
mondo:0015239,abnormal origin of the pulmonary artery,,,,1138,,,,,,,,,
mondo:0015240,digitotalar dysmorphism,"['DA1', 'distal arthrogryposis type 1', 'AMCD1', 'digitotalar dysmorphism', 'arthrogryposis multiplex congenita distal type 1', 'distal arthrogryposis type 1A (sub-type)', 'distal arthrogryposis type 1B (sub-type)']",0111596,,1146,CN197602,"['0.05014', '0.04095', '-0.2708', '-0.0444', '0.1809', '-0.4502', '0.2114', '1.073', '-1.07', '-0.3496', '-0.28', '0.0515', '-0.3918', '0.4197', '0.2062', '0.3276', '-0.0728', '-0.3516', '-0.359', '-1.061', '-0.411', '0.10614', '0.8237', '0.1001', '0.11346', '0.1622', '-0.1644', '0.3796', '0.298', '-0.2703', '0.616', '-0.4255', '-0.1462', '1.0', '0.112', '-0.312', '0.1338', '0.0045', '0.1433', '0.0943', '-0.115', '-0.4524', '0.2231', '0.256', '0.4363', '-0.07294', '-0.1682', '-0.1406', '-0.1289', '-0.1897', '-0.2595', '-0.8164', '-0.0906', '-0.5923', '-0.4934', '-0.452', '0.02344', '-0.5312', '0.2727', '-0.5806', '-0.1236', '-0.012764', '0.089', '0.1205', '-0.3284', '0.10126', '0.2188', '-0.1466', '0.2747', '0.12286', '-0.51', '0.2576', '0.04034', '0.0624', '0.2913', '0.4382', '0.4517', '-0.1954', '-0.8394', '-0.332', '-0.262', '0.4253', '0.516', '0.825', '-0.3801', '0.9365', '-0.01301', '0.443', '-0.2827', '-0.456', '-0.402', '0.05307', '0.2886', '0.1375', '0.3025', '0.2012', '0.586', '-0.967', '0.2384', '-0.08527']",,,C565097,,,,
mondo:0015241,arthrogryposis-like syndrome,"['Kuskokwim syndrome', 'arthrogryposis like disorder', 'Kuskokwim disease']",,208200,1149,,,,,,719.89,,,
mondo:0015243,allergic bronchopulmonary aspergillosis,"['pulmonary aspergillus disease', 'allergic bronchopulmonary mycosis', 'aspergillosis, allergic bronchopulmonary', 'Hinson-Pepys disease', 'allergic aspergillosis', 'allergic bronchopulmonary aspergillosis, familial', 'ABPA']",13166,103920,1164,C0004031,,C84547,0007140,D001229,518.6,B44.81,10006474,
mondo:0015244,autosomal recessive cerebellar ataxia,"['cerebellar ataxia, autosomal recessive', 'arca']",0050950,,1172,CN226644,"['-0.0885', '-0.2139', '-0.0966', '0.1962', '-0.1749', '-0.7773', '0.3486', '0.1448', '-0.6294', '-0.911', '0.010605', '0.08466', '-0.1254', '0.1627', '0.4055', '-0.1459', '-0.09326', '-0.3', '0.1699', '-0.75', '-0.1768', '-0.248', '0.3376', '-0.6895', '0.377', '-0.62', '-0.3608', '0.1794', '-0.0376', '-0.972', '0.137', '0.411', '-0.6035', '-0.146', '0.2888', '0.2131', '-0.1072', '0.1602', '0.3813', '0.7334', '0.1737', '0.1482', '-0.3928', '0.3005', '0.6694', '-0.659', '0.08307', '0.465', '0.2338', '0.1534', '-0.09424', '0.04193', '0.0367', '-0.3386', '-0.03958', '-0.747', '0.4792', '0.5664', '-0.1521', '0.4136', '-0.4802', '0.179', '0.1427', '-0.073', '-0.3887', '0.517', '0.2344', '0.69', '-0.4717', '0.4788', '0.761', '0.493', '-0.003876', '-0.752', '0.735', '0.3738', '0.2947', '0.1769', '-0.0289', '0.596', '-0.317', '-0.9307', '0.3538', '0.7227', '-0.2546', '-0.7754', '0.3613', '0.01907', '0.4067', '0.54', '0.567', '0.4827', '0.01707', '-0.1357', '0.903', '0.773', '0.4646', '0.4465', '-0.3105', '0.02031']",,,,,,,
mondo:0015246,syndromic anorectal malformation,"['syndrome associated with anorectal malformation', 'syndromic anorectal malformation']",,,117573,CN226645,,,,,,,,
mondo:0015247,opsoclonus-myoclonus syndrome,"['oma syndrome', 'dancing eye-dancing feet syndrome', 'dancing eye syndrome', 'opsoclonus-myoclonus-ataxia syndrome', 'POMA syndrome', 'Kinsbourne syndrome', 'opsoclonus myoclonus syndrome', 'OMS', 'paraneoplastic opsoclonus-myoclonus-ataxia syndrome', 'Ataxo-opso-myoclonus syndrome', 'paraneoplastic opsoclonus-myoclonus']",,,1183,C0393626,,C4686,1001383,D053578,379.59,,10053854,
mondo:0015248,ataxia-photosensitivity-short stature syndrome,['Fenton-Wilkinson-Toselano syndrome'],,,1184,CN237421,,,,,,,,
mondo:0015249,mitral atresia disorder,"['congenital atresia of mitral valve', 'mitral atresia', 'congenital mitral valve atresia', 'mitral valve atresia']",,,1205,,,C98992,,,,Q23.2,,0011560
mondo:0015250,spinal atrophy-ophthalmoplegia-pyramidal syndrome,"['infantile progressive spinal muscular atrophy with ophthalmoplegia and pyramidal symptoms', 'spinal atrophy ophthalmoplegia pyramidal syndrome', 'Hamano Tsukamoto syndrome', 'Hamano-Tsukamoto syndrome']",,,1217,C2930956,,,,C535625,,,,
mondo:0015252,severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome,"['severe microbrachycephaly-intellectual disability-athetoid cerebral palsy syndrome', 'BD syndrome', 'intellectual disability-athetosis-microphthalmia syndrome', 'intellectual disability - athetosis - microphthalmia']",,,1236,CN237422,,,,,,,,
mondo:0015253,Diamond-Blackfan anemia,"['anemia Diamond Blackfan type', 'congenital hypoplastic anemia', 'aregenerative anemia chronic congenital', 'anaemia congenital erythroid hypoplastic', 'congenital PRCA', 'Blackfan Diamond syndrome', 'Aase syndrome', 'DBA', 'aregenerative anaemia chronic congenital', 'inherited erythroblastopenia', 'anaemia Diamond Blackfan type', 'erythrogenesis imperfecta', 'chronic constitutional pure red cell anaemia', 'chronic constitutional pure red cell anemia', 'BDS', 'Blackfan - Diamond syndrome', 'anemia congenital erythroid hypoplastic', 'Blackfan-Diamond anaemia', 'Blackfan-Diamond anemia', 'Red cell aplasia, pure hereditary', 'congenital hypoplastic anaemia', 'congenital hypoplastic anemia, Blackfan-Diamond type', 'Aase-Smith II syndrome', 'congenital pure red cell aplasia']",1339,,124,C1260899,"['-0.3906', '0.3657', '-0.2318', '0.278', '0.6167', '0.2817', '-0.1447', '0.627', '-0.4575', '-0.7725', '0.488', '-0.2058', '0.608', '0.6113', '-1.157', '0.2067', '-0.8276', '0.11914', '-0.462', '-0.3474', '-0.2294', '-0.4304', '0.5557', '-0.3691', '0.454', '-0.2051', '-0.04352', '-0.2512', '0.47', '0.08356', '0.263', '0.0781', '0.4875', '0.603', '0.5303', '-0.3306', '-0.299', '-0.722', '0.1715', '-0.2449', '-0.6826', '0.4446', '-0.01177', '-0.5913', '-0.585', '-0.5024', '0.289', '0.09607', '0.1704', '-0.3274', '0.4358', '0.11', '0.6733', '-0.142', '0.575', '-0.5684', '0.01322', '0.402', '-0.9805', '-0.0462', '0.0965', '0.2191', '-0.1589', '-0.181', '0.10236', '0.1947', '0.2094', '0.562', '-0.533', '1.042', '0.757', '-0.449', '-0.616', '-0.884', '0.3203', '0.9517', '0.211', '0.0861', '-0.0714', '0.196', '0.151', '-0.1929', '-0.01182', '0.1268', '0.3574', '-0.4148', '-0.3906', '0.3145', '0.903', '-0.4485', '0.4895', '0.2622', '-0.02731', '-0.099', '0.7256', '0.804', '-0.094', '0.0427', '0.281', '-0.414']",C61236,,D029503,,,10062989,
mondo:0015254,schistosomiasis,"['Bilharzia', 'bilharziasis', 'schistosomiasis', 'snail fever']",1395,,1247,C0036323,,C35000,1001475,D012552,120.9,,10039603,
mondo:0015255,blepharophimosis-radioulnar synostosis syndrome,"['mild short stature, microcephaly, ptosis-blepharophimosis, facial asymmetry, and radioulnar synostosis', 'Jorgenson Lenz syndrome', 'blepharophimosis radioulnar synostosis', 'ptosis, prognathism, microcephaly, radio-ulnar synostosis, short stature/dwarfism', 'Jorgenson-Lenz syndrome']",,,1256,C2931162,,,,C536292,,,,
mondo:0015256,blepharoptosis-cleft palate-ectrodactyly-dental anomalies syndrome,['Rodini-Richieri Costa syndrome'],,,1258,,,,,,,,,
mondo:0015257,sino-auricular heart block,,,,1260,CN199152,,,,,,,,
mondo:0015259,brachydactyly-mesomelia-intellectual disability-heart defects syndrome,"['brachydactyly mesomelia mental retardation aortic dilatation mitral valve prolapse and characteristic face', 'brachydactyly mesomelia intellectual disability aortic dilatation mitral valve prolapse and characteristic face', 'Stratton-Garcia-Young syndrome']",,,1277,CN199165,,,,,,,,
mondo:0015260,diphyllobothriasis,"['fish tapeworm', 'Diphyllobothrium infection', 'Diphyllobothrium caused disease or disorder', 'Bothriocephalosis']",10075,,128,C0012561,,C128391,0007238,D004169,123.4,B70.0,10013029,
mondo:0015261,pseudopelade of Brocq,"['pseudo-pelade of Brocq', 'pseudo pelade of Brocq', 'Brocq pseudopelade']",,,129,,,,,C531609,704.09,,,
mondo:0015262,brachyolmia,['brachyrachia'],0050690,,1293,C0432228,"['-0.1016', '0.2118', '0.1709', '-0.1863', '0.364', '-0.5425', '0.05286', '0.7085', '-0.0942', '-0.356', '-0.191', '-0.3105', '-0.4954', '0.3071', '0.5386', '0.3237', '0.416', '-0.09607', '-0.3406', '-0.699', '-0.4014', '0.326', '0.85', '-0.1638', '-0.3433', '0.05865', '0.325', '-0.3113', '0.1907', '0.03644', '0.1028', '-0.6265', '-0.1721', '0.3733', '0.3887', '-0.3103', '-0.4854', '-0.707', '0.1043', '0.0959', '0.3137', '-0.5503', '0.2957', '0.2161', '0.622', '-0.503', '-0.05392', '0.497', '0.0872', '-0.11285', '1.052', '-0.0545', '0.0863', '0.2399', '-0.0798', '-0.5225', '-0.2551', '-0.2074', '-0.0214', '0.266', '0.623', '-0.386', '-0.5', '-0.3325', '-0.05167', '-0.1528', '-0.1383', '0.5645', '-0.12317', '0.372', '0.01079', '-0.2996', '-0.1277', '-0.1632', '0.5576', '0.668', '-0.06256', '-0.1346', '-0.1556', '-0.04562', '0.4883', '0.1624', '-0.225', '0.484', '-0.0953', '0.0992', '0.08966', '0.06866', '0.4685', '0.1329', '0.01793', '0.2744', '-0.05142', '0.1145', '0.5156', '0.2117', '0.4915', '-0.6973', '0.1719', '-0.0817']",,,C537098,756.19,,,
mondo:0015263,Brugada syndrome,"['dream disease', 'sudden unexplained nocturnal death syndrome', 'SUNDS', 'Pokkuri death syndrome', 'idiopathic ventricular fibrillation, Brugada type', 'right bundle branch block, ST segment elevation, and sudden death syndrome', 'Bangungut', 'Brugada syndrome', 'sudden unexpected nocturnal death syndrome', 'Brugada type idiopathic ventricular fibrillation']",0050451,,130,C1142166,"['0.007023', '-0.1151', '-0.8213', '0.002207', '-0.18', '-0.1115', '0.3662', '0.647', '0.3613', '-0.73', '-0.07764', '-0.1643', '-0.1877', '0.3997', '-0.7876', '0.3303', '-0.7695', '-0.117', '-0.3865', '-0.01636', '-0.01105', '0.10876', '0.807', '0.1062', '0.1542', '-0.2225', '-0.265', '0.05212', '-0.07404', '0.0671', '0.822', '-0.08026', '0.2058', '0.3533', '-0.2458', '-0.4077', '0.2152', '0.1183', '0.7725', '-0.8906', '0.795', '0.2115', '0.0678', '-0.3772', '0.1305', '-0.261', '-1.156', '-0.1437', '-0.4656', '0.1685', '-0.2896', '-0.1511', '-0.3433', '-0.738', '0.0481', '-0.4136', '-0.03128', '0.3247', '-0.2559', '-0.11084', '0.1934', '0.807', '0.4556', '-0.2683', '-0.1294', '0.731', '-0.10394', '0.1683', '-0.4006', '0.549', '-0.779', '0.3145', '0.06186', '-0.3398', '-0.2069', '0.5396', '0.2869', '0.02492', '-0.3289', '-0.56', '0.491', '0.1893', '-0.01968', '0.05554', '0.3044', '-0.438', '0.5366', '0.01778', '0.1004', '0.3364', '0.372', '-0.2646', '-0.02766', '0.4019', '0.8037', '0.2935', '-0.01421', '-0.51', '-1.326', '-0.03247']",C142891,,D053840,746.89,,10059027,
mondo:0015264,cryptogenic organizing pneumonia,"['bronchiolitis obliterans organizing pneumonia', 'cryptogenic organizing pneumonitis', 'organising pneumonia', 'bronchiolitis obliterans organising pneumonia', 'idiopathic bronchiolitis obliterans with organizing pneumonia', 'organizing pneumonia', 'idiopathic bronchiolitis obliterans organizing pneumonia', 'idiopathic bronchiolitis obliterans with organising pneumonia', 'cryptogenic organising pneumonitis', 'constrictive bronchiolitis', 'idiopathic BOOP', 'idiopathic bronchiolitis obliterans organising pneumonia', 'COP']",0050157,,1302,C0242770,,C62586,1001300,D018549,516.36,J84.116,,
mondo:0015265,bronchiolitis obliterans syndrome,"['bronchiolitis exudativa', 'organising pneumonia', 'BOOP', 'BO', 'organised pneumonia', 'organizing pneumonia', 'bronchiolitis obliterans', 'obliterative bronchiolitis', 'constrictive bronchiolitis', 'bronchiolitis obliterans with obstructive pulmonary disease', 'bronchiolitis fibrosa obliterans']",2799,,1303,CN199179,,,0007183,,491.8,,,0011946
mondo:0015267,Feingold syndrome,"['MMT', 'ODED syndrome', 'MODED syndrome', 'FGLDS', 'FS', 'digital anomalies with short palpebral fissures and atresia of esophagus or duodenum', 'microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome', 'oculo-digito-esophageal-duodenal syndrome', 'microcephaly-digital anomalies-normal intelligence syndrome', 'microcephaly-oculo-digito-esophageal-duodenal syndrome', 'Brunner-Winter syndrome', 'digital anomalies with short palpebral fissures and atresia of esophagus, or duodenum', 'microcephaly-intellectual disability-tracheoesophageal fistula syndrome', 'digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum']",0060464,,1305,,"['0.252', '-0.0787', '0.3513', '-0.4', '0.2102', '-0.1499', '0.1292', '0.1139', '-0.58', '0.1501', '-0.27', '-0.1156', '-0.507', '-0.03308', '-0.2319', '-0.06604', '0.3623', '-0.086', '-0.05527', '-0.6094', '-0.0873', '0.3225', '0.4302', '-0.2578', '0.2983', '0.3303', '-0.2954', '-0.1675', '0.1985', '-0.3677', '0.726', '-0.4753', '0.01743', '0.3025', '0.2766', '-0.2932', '-0.3438', '-0.186', '-0.3389', '0.01802', '0.299', '-0.619', '0.3499', '-0.2012', '0.1364', '-0.2301', '0.0416', '0.4304', '-0.0672', '-0.1846', '-0.12054', '-0.6294', '-0.2747', '-0.1862', '-0.2147', '-0.3464', '-0.1827', '0.0269', '-0.3752', '0.1252', '-0.03995', '0.1338', '0.1948', '0.2988', '-0.1863', '-0.2532', '-0.3064', '0.00475', '-0.6753', '0.2439', '-0.775', '0.2976', '-0.0032', '0.011505', '0.4558', '0.1554', '-0.2502', '-0.4136', '-0.511', '-0.133', '0.12317', '0.3264', '-0.0857', '0.29', '-0.1921', '0.2769', '0.1755', '0.673', '0.2239', '-0.338', '-0.2632', '0.659', '0.622', '-0.3374', '0.9624', '-0.0702', '0.3452', '-0.7637', '0.301', '0.131']",C74987,,,,,,
mondo:0015268,medullary sponge kidney,"['Precalyceal canalicular ectasia', 'sponge kidney', 'Cacchi-Ricci syndrome', 'Precalicial canalicular ectasia', 'Cacchi Ricci disease', 'MSK', 'Cacchi-Ricci disease', 'cystic dilatation of renal collecting tubes']",,,1309,C0022681,,C34751,,D007691,753.17,,10027104,
mondo:0015269,symmetrical thalamic calcifications,['bilateral symmetrical thalamic gliosis'],,,1314,C4304914,,,,,,,,
mondo:0015270,butyrylcholinesterase deficiency,"['butyrylcholinesterase deficiency, fluoride-resistant, Japanese type', 'succinylcholine sensitivity', 'butyrylcholinesterase deficiency', 'hypocholinesterasemia, fluoride-resistant, Japanese type', 'BCHED', 'pseudocholinesterase E1', 'pseudocholinesterase deficiency', 'cholinesterase 2 deficiency', 'Suxamethonium sensitivity', 'Acholinesterasemia', 'apnea, postanesthetic, susceptibility to, due to BCHE deficiency', 'apnea, postanesthetic']",,617936,132,C1283400,"['-0.3508', '0.06177', '-0.7593', '0.3162', '0.119', '0.0171', '0.8643', '0.6494', '-0.3232', '0.01619', '0.12164', '0.303', '0.382', '-0.05554', '0.03403', '0.1108', '0.2196', '-0.000804', '-0.237', '-0.6606', '0.0426', '-0.1231', '0.91', '-0.03403', '-0.02489', '-0.525', '-0.1075', '-0.1447', '-0.594', '0.007782', '0.3174', '0.03363', '0.374', '0.2905', '-0.403', '-0.3696', '0.0225', '-0.3455', '0.05005', '0.1009', '0.2878', '-0.4788', '0.276', '0.261', '-0.02771', '0.276', '0.00533', '-0.1661', '0.0692', '0.6646', '-0.1915', '-0.6733', '0.04242', '-0.3384', '-0.1832', '0.12317', '0.545', '-0.3162', '-0.1301', '-0.4412', '0.051', '0.4973', '0.3728', '0.01692', '0.004265', '0.126', '0.11554', '-0.05905', '-0.2937', '-0.3965', '0.1559', '0.03458', '0.2075', '-0.4976', '0.3953', '0.514', '0.4016', '-0.1533', '-0.1417', '-0.2241', '0.152', '-0.1805', '0.2732', '-0.0695', '0.10486', '0.4307', '0.3477', '0.3772', '0.4507', '-0.2014', '0.2382', '-0.308', '0.2316', '0.003132', '0.8525', '0.1732', '0.0755', '-0.506', '-0.6807', '0.02328']",,,C537417,289.89,,,
mondo:0015271,idiopathic camptocormia,"['idiopathic progressive lumbar kyphosis', 'bent spine', 'bent spine syndrome', 'camptocormia', 'idiopathic camptocormism', 'camptocormism']",,,1320,,,,,C537968,,,10069646,
mondo:0015272,camptodactyly-taurinuria syndrome,"['camptodactyly with taurinuria', 'camptodactyly taurinuria', 'familial streblodactyly with amino-aciduria']",,,1325,C2931681,,,,C537972,,,,
mondo:0015273,complete atrioventricular canal,"['CAVC', 'complete atrioventricular septal defect']",,,1329,,,,,C535974,745.69,,,
mondo:0015274,chronic beryllium disease,"['Beryllliosis', 'acute berylliosis', 'chronic beryllium lung disease', 'berylliosis', 'chronic berylliosis', 'Subacute berylliosis', 'beryllium disease', 'reversible berylliosis', 'beryllium poisoning', 'chronic pulmonary berylliosis']",10322,,133,,,,0007168,D001607,503,,10004485,
mondo:0015275,partial atrioventricular canal,"['partial common atrioventricular canal', 'partial atrioventricular canal defect', 'partial AVSD', 'PAVC', 'partial atrioventricular septal defects']",,,1330,,,,,C536112,,,,
mondo:0015277,medullary thyroid gland carcinoma,"['thyroid gland medullary carcinoma', 'C cell carcinoma', 'medullary carcinoma of the thyroid gland', 'medullary thyroid cancer', 'carcinoma of parafollicular cell', 'THME', 'thyroid carcinoma, medullary', 'medullary thyroid cancer (MTC)', 'ultimobranchial thyroid tumour', 'MTC', 'thyroid cancer, medullary', 'medullary carcinoma of thyroid', 'medullary carcinoma of thyroid gland', 'ultimobranchial thyroid tumor', 'thyroid gland medullary cancer', 'parafollicular cell carcinoma', 'medullary thyroid carcinoma', 'carcinoma, C-cell, malignant', 'thyroid gland neuroendocrine carcinoma', 'medullary thyroid gland carcinoma', 'thyroid medullary carcinoma', 'medullary carcinoma of the thyroid', 'medullary carcinoma']",3973,,1332,C0238462,,C3879,,,,,10027101,0002865
mondo:0015278,familial pancreatic carcinoma,"['familial pancreatic cancer', 'hereditary pancreatic carcinoma', 'pancreatic cancer, somatic', 'hereditary pancreatic cancer', 'hereditary exocrine pancreatic carcinoma', 'pancreatic carcinoma, somatic', 'familial pancreatic carcinoma', 'pancreatic acinar carcinoma']",,260350,1333,C2931038,"['0.06125', '-0.2222', '-0.2627', '-0.1987', '0.1522', '-0.0738', '0.2418', '0.332', '-0.3186', '0.2279', '-0.01776', '0.05725', '-0.2236', '0.2017', '-0.53', '-0.5723', '-0.4626', '-0.4124', '-0.035', '-0.3748', '-0.1954', '-0.5103', '0.92', '-1.04', '0.563', '0.3574', '0.2216', '0.2284', '0.0535', '-0.2708', '0.586', '-0.1971', '-0.2556', '-0.2302', '0.0688', '-0.0161', '-0.4043', '0.216', '-0.2422', '0.384', '-0.06207', '0.12366', '0.371', '-0.3875', '0.7188', '0.323', '-0.4783', '0.04935', '-0.07074', '-0.1157', '-0.00863', '0.1525', '-0.0825', '0.104', '-0.3325', '-0.05884', '0.3564', '-0.2883', '-0.4263', '-0.0166', '0.651', '0.185', '-0.0914', '-0.305', '-0.1185', '0.396', '0.3022', '0.194', '0.173', '0.5093', '0.01111', '0.2866', '0.0655', '-0.0849', '0.879', '-0.01092', '-0.2983', '0.0726', '-0.2228', '-0.701', '-0.6826', '-0.2505', '-0.4832', '-0.2664', '-0.1263', '-0.48', '0.931', '0.001382', '0.0457', '-0.1772', '0.489', '0.0921', '0.07245', '-0.1228', '1.192', '-0.117', '0.10095', '-0.446', '-0.356', '0.04068']",C43298,,C535837,,,,
mondo:0015279,chronic mucocutaneous candidiasis,"['CANDF', 'CMC', 'chronic mucocutaneous candidiasis', 'familial chronic mucocutaneous candidiasis', 'familial candidiasis', 'chronic mucocutaneous candidiasis (disease)', 'familial CMC']",2058,,1334,C0006845,,C34444,,D002178,,,10009007,0002728
mondo:0015280,cardiofaciocutaneous syndrome,"['congenital heart defects characteristic facial appearance ectodermal abnormalities and growth failure', 'cardiofaciocutaneous (CFC) syndrome', 'CFC', 'cardio-facio-cutaneous syndrome', 'CFC syndrome', 'cardio-facial-cutaneous syndrome']",0060233,,1340,C1275081,"['0.1826', '-0.3997', '0.3853', '-0.3835', '0.0812', '-0.3494', '0.2144', '0.843', '-0.3716', '-0.677', '0.4382', '-0.02174', '-0.052', '-0.2632', '-0.4612', '-0.03226', '0.12225', '-0.6636', '-0.2798', '-0.5728', '-0.2605', '-0.2634', '0.177', '-0.2642', '-0.2068', '-0.2263', '-0.678', '0.2786', '0.6934', '0.003027', '0.585', '-0.4382', '0.514', '-0.004044', '-0.2888', '0.07635', '0.2377', '0.081', '-0.11005', '0.33', '-0.1006', '-0.1667', '0.3057', '0.2474', '0.3137', '-0.0121', '0.07043', '0.2043', '0.2803', '0.1232', '-0.765', '0.262', '-0.03253', '-0.02875', '-0.556', '0.02792', '0.01573', '-0.006252', '-0.2277', '0.02797', '-0.155', '0.3337', '-0.06366', '0.08856', '0.4495', '0.1908', '0.2986', '0.5615', '-0.2433', '0.445', '-0.2534', '-0.11865', '-0.3423', '0.2498', '-0.2178', '-0.3103', '0.2915', '-0.965', '-0.2383', '-0.2308', '0.7554', '-0.2637', '-0.2607', '0.5107', '-0.4817', '0.10376', '0.5483', '-0.07825', '0.7524', '0.8306', '0.2415', '0.383', '0.05347', '0.7905', '0.5093', '-0.0981', '0.2793', '0.0735', '0.4414', '-0.02945']",C84617,,C535579,,,,
mondo:0015281,atrial standstill,['atrial cardiomyopathy with heart block'],,,1344,CN199216,"['-0.6045', '0.3923', '-0.2778', '0.064', '-0.2927', '-0.03326', '0.5996', '0.5107', '0.0808', '0.2086', '-0.399', '-0.5293', '-0.299', '-0.1989', '-0.3555', '-0.007126', '-0.3252', '-0.1699', '-0.3096', '-0.635', '0.0897', '0.463', '0.4832', '-0.2725', '0.2607', '-0.1523', '0.2283', '0.2247', '0.0759', '0.1897', '0.4165', '0.4736', '0.4185', '0.2355', '-0.277', '-0.314', '0.4524', '0.0863', '0.3145', '-0.5166', '0.2893', '-0.006588', '0.3374', '0.06137', '0.1875', '-0.1544', '-0.449', '0.5044', '-0.1038', '0.4583', '-0.05502', '0.1643', '-0.2123', '0.1565', '-0.3418', '-0.2954', '0.1564', '-0.11414', '-0.06323', '-0.1863', '0.0625', '0.279', '0.2559', '-0.2925', '-0.02351', '0.00692', '0.4397', '0.4294', '-0.6123', '-0.10803', '-0.417', '0.23', '0.354', '-0.003288', '-0.06085', '0.2223', '0.448', '0.0718', '-0.5874', '-0.06415', '0.04968', '0.0655', '0.3435', '-0.3547', '0.581', '-0.08276', '0.0675', '0.4026', '-0.01874', '0.04498', '0.0804', '0.10266', '-0.3582', '0.302', '0.882', '0.04288', '0.3418', '-0.4282', '-0.3303', '0.2483']",,,C563984,426.6,,,
mondo:0015282,cardiomyopathy-cataract-hip spine disease syndrome,"['familial dilated cardiomyopathy associated with cataracts and hip-spine disease', 'Krasnow Qazi Yermakov syndrome', 'Krasnow Qazi syndrome', 'cardiomyopathy cataract hip spine disease', 'Krasnow-Qazi syndrome']",,,1345,C2931548,,,,C537616,,,,
mondo:0015283,maternally-inherited cardiomyopathy and hearing loss,"['maternally-inherited cardiomyopathy and deafness', 'tRNA-LYS-related cardiomyopathy-hearing loss syndrome']",,,1349,CN199218,,,,,,,,
mondo:0015284,heart-hand syndrome type 2,"['Tabatznik syndrome', 'atriodigital dysplasia type 2', 'heart-hand syndrome 2']",,,1350,C2931323,,,,C536784,,,,
mondo:0015285,Carney complex,"['Carney syndrome', 'nevi, atrial myxoma, skin myxoma, ephelides syndrome', 'atrial myxoma with lentigines', 'lamb', 'Carney Complex, type 2', 'Myxoma - spotty pigmentation - endocrine overactivity', 'lamb syndrome', 'CNC', 'NAME syndrome', 'Myxoma-spotty pigmentation-endocrine overactivity syndrome', 'Carney Complex, type 1', 'Carney^s syndrome', 'lentigines, atrial myxoma, mucocutaneous myoma, blue Nevus syndrome']",0050471,,1359,C0406810,"['-0.2717', '-0.2744', '-0.263', '-0.4895', '0.4321', '0.0822', '0.2847', '-0.1876', '-0.847', '-0.572', '0.395', '-0.05075', '-0.4548', '0.3062', '-0.1067', '0.002792', '-0.2295', '-0.305', '0.07056', '-0.4185', '0.1534', '-0.494', '0.371', '-0.2036', '0.2186', '0.645', '-0.1615', '0.0533', '0.4807', '0.05292', '0.497', '-0.072', '0.668', '0.11664', '-0.1896', '-0.07776', '0.2028', '0.2852', '0.1549', '0.0715', '0.608', '-0.09045', '1.062', '-0.2172', '0.4382', '-0.4368', '0.417', '-0.07697', '0.6504', '0.0258', '0.1029', '-0.1566', '0.1615', '0.12305', '-0.817', '0.4216', '0.3684', '-0.3088', '-0.635', '0.1713', '0.5073', '0.3965', '-0.2737', '-0.5234', '-0.006786', '0.5635', '0.2029', '0.163', '-0.3718', '0.02757', '-0.3389', '0.07104', '-0.02863', '0.2424', '0.06177', '-0.2944', '0.03598', '0.3416', '-0.3933', '-0.2917', '0.441', '-0.0235', '-0.4011', '-0.04733', '-0.52', '-0.665', '0.6094', '-0.284', '0.2847', '0.4067', '0.2032', '-0.2002', '0.1886', '-0.1932', '1.389', '-0.349', '0.6753', '0.014725', '0.1532', '0.1738']",C4705,,D056733,,D44.8,,
mondo:0015286,congenital disorder of glycosylation,"['carbohydrate-deficient glycoprotein syndromes', 'carbohydrate-deficient glycoprotein syndrome', 'CDG', 'congenital disorders of glycosylation', 'carbohydrate deficient glycoprotein syndrome']",5212,,137,C0282577,"['-0.582', '0.3188', '0.3455', '0.2034', '0.5454', '-0.3599', '-0.276', '-0.1764', '-0.3118', '0.1995', '-0.4058', '-0.2878', '0.3535', '0.06088', '-0.278', '0.4104', '-0.253', '-0.323', '-0.4468', '-0.7256', '0.65', '0.1031', '0.5444', '-0.2715', '-0.000986', '-0.531', '-0.1849', '-0.801', '-0.1578', '-0.1287', '0.1696', '0.5747', '0.4019', '0.04987', '-0.2015', '0.01265', '-0.3477', '0.3079', '-0.6655', '-0.665', '0.2522', '-0.5728', '-0.2502', '0.1229', '0.2869', '-1.037', '0.503', '0.03992', '0.31', '0.1239', '-0.1488', '0.2703', '0.3794', '0.1615', '-0.5894', '-0.374', '0.4875', '0.522', '-0.7905', '0.1298', '0.2073', '-0.03644', '0.3152', '0.1287', '-0.03485', '-0.0821', '-0.05402', '0.1908', '-0.262', '-0.394', '0.04282', '0.3064', '-0.2053', '-0.0135', '-0.12225', '0.3118', '0.04376', '0.1345', '-0.685', '-0.3896', '0.1893', '-0.02756', '-0.5527', '0.2283', '-0.01114', '-0.4072', '0.2213', '-0.2563', '-0.02872', '-0.2035', '0.2563', '0.2166', '-0.10486', '-0.3818', '0.375', '0.9404', '0.4492', '-0.1534', '0.1384', '0.7847']",C84615,,D018981,271.8,,,
mondo:0015288,herpes simplex virus keratitis,"['herpetic keratitis', 'HSV keratitis', 'Simplexvirus caused keratitis', 'dendritic keratitis']",0080158,,137586,C0022570,,C34743,0007308,,,,,
mondo:0015289,infectious epithelial keratitis,,,,137593,,,,,,,,,
mondo:0015290,neurotrophic keratopathy,['neurotrophic keratitis'],,,137596,C0339296,,,,,,H16.2,10069732,
mondo:0015291,stromal keratitis,,,,137599,C1318020,,,,,,,,
mondo:0015292,endotheliitis,['endothelium inflammation'],,,137602,,,,,,,,,
mondo:0015293,segmental outgrowth-lipomatosis-arteriovenous malformation-epidermal nevus syndrome,['SOLAMEN syndrome'],,,137608,CN199243,,,,,,,,
mondo:0015294,nephrogenic systemic fibrosis,"['NSF', 'nephrogenic fibrosing dermopathy', 'NFD']",,,137617,C3888044,,C84920,1001814,D054989,588.89,,10067467,
mondo:0015295,intractable diarrhea-choanal atresia-eye anomalies syndrome,,,,137622,CN226653,,,,,,,,
mondo:0015296,cardiac anomalies-heterotaxy syndrome,,,,137628,CN199246,,,,,,,,
mondo:0015298,pellucid marginal degeneration,,,,137672,CN199253,,,,,,,,
mondo:0015299,Asherman syndrome,"['Asherman^s syndrome', 'intrauterine adhesions', 'intrauterine synechiae', 'uterine synechiae', 'Asherman syndrome']",,,137686,C0156372,,,,,,,10053868,
mondo:0015300,cataract - microcornea syndrome,"['cataract microcornea syndrome', 'microcornea cataract syndrome']",,,1377,,,,,C538287,,,,
mondo:0015301,primary cutaneous amyloidosis,"['amyloidosis, primary localised cutaneous', 'PLCA', 'amyloidosis IX', 'familial primary localized cutaneous amyloidosis', 'primary localised cutaneous amyloidosis', 'amyloidosis familial cutaneous lichen', 'primary localized cutaneous amyloidosis', 'familial primary localised cutaneous amyloidosis', 'amyloidosis, primary localized cutaneous', 'lichen amyloidosis familial']",0050639,,137807,C0268397,,,,C562642,,,10011659,
mondo:0015302,nodular cutaneous amyloidosis,"['amyloidosis nodular localised cutaneous', 'amyloidosis nodular localized cutaneous', 'primary localized cutaneous nodular amyloidosis', 'NLCA', 'PLCNA', 'primary localised cutaneous nodular amyloidosis', 'amyloidosis cutis nodularis atrophicans']",,,137810,C4274331,,,,,,,10056953,
mondo:0015303,macular amyloidosis,,,,137814,C0544839,,,,,,,,
mondo:0015304,arachnoiditis,"['adhesive arachnoiditis', 'arachnoid mater inflammation', 'chronic arachnoiditis']",12156,,137817,C0270617,,C37913,,D001100,,,10003074,
mondo:0015306,Lemierre syndrome,"['acute sore throat', 'postanginal sepsis', 'necrobacillosis', 'Lemierre postanginal sepsis', 'postanginal sepsis secondary to orophyngeal infection', 'septic phlebitis of the internal jugular vein', 'oropharyngeal infection leading to secondary septic thrombophlebitis of the internal jugular vein', 'Lemierre syndrome', 'human necrobacillosis', 'Lemierre^s syndrome']",11337,,137839,,,,,D057831,040.3,,10065552,
mondo:0015307,Madras motor neuron disease,['MMND'],,,137867,C0393551,,,,,,,,
mondo:0015308,laminopathy type Decaudain-Vigouroux,['laminopathy with severe metabolic syndrome and myopathy'],,,137871,C4518324,,,,,,,,
mondo:0015310,syndromic optic nerve hypoplasia,,,,137905,CN226655,,,,,,,,
mondo:0015311,autism-facial port-wine stain syndrome,['autism with port-wine stain'],,,137911,CN199278,,,,,,,,
mondo:0015312,"choanal atresia, unilateral",,,,137917,CN199280,,,,,,,,
mondo:0015313,"choanal atresia, bilateral",,,,137920,CN199281,,,,,,,,
mondo:0015314,primary laryngeal lymphangioma,,,,137926,,,,,,,,,
mondo:0015315,neonatal brainstem dysfunction,,,,137929,CN199283,,,,,,,,
mondo:0015316,congenital laryngeal palsy,['congenital vocal cord paralysis'],,,137932,C0396058,,,,,,,,
mondo:0015317,laryngotracheal angioma,,,,137935,C3839574,,,,,228.09,,,
mondo:0015323,teratogenic Pierre Robin syndrome,['teratogenic Pierre Robin sequence'],,,138059,CN199294,,,,,,,,
mondo:0015324,cataract-intellectual disability-anal atresia-urinary defects syndrome,"['cataract mental retardation anal atresia urinary defects', 'cataract intellectual disability anal atresia urinary defects', 'Karandikar Maria Kamble syndrome', 'Karandikar-Maria-Kamble syndrome', 'congenital cataract with multiple congenital anomalies in a sibship']",,,1381,C2931391,,,,C537009,,,,
mondo:0015325,cataract-deafness-hypogonadism syndrome,"['cataracts, sensorineural deafness, hypogonadism, hypertrichosis and short stature', 'Schaap-Taylor-Baraitser syndrome']",,,1383,,,,,C536626,,,,
mondo:0015326,night blindness-skeletal anomalies-dysmorphism syndrome,"['Hunter-Thompson-Reed syndrome', 'Hunter Thompson Reed syndrome']",,,1390,CN199356,,,,,,,,
mondo:0015327,developmental anomaly of metabolic origin,,,,139009,,,,,,,,,
mondo:0015330,overgrowth/obesity syndrome,,,,139024,CN199360,,,,,,,,
mondo:0015333,progeroid syndrome,,0081332,,139033,CN199363,,,,,,,,
mondo:0015334,branchial arch or oral-acral syndrome,,,,139036,CN199364,,,,,,,,
mondo:0015337,isolated craniosynostosis,['nonsyndromic craniosynostosis'],,,139390,,"['0.23', '-0.0719', '-0.2913', '0.4578', '0.3645', '-0.3875', '0.1825', '0.6025', '-1.053', '-0.5513', '0.0194', '-0.2537', '0.2476', '0.8765', '-0.2546', '-0.1891', '0.594', '-0.467', '-0.1077', '-1.281', '0.02519', '0.6626', '0.3623', '-0.6', '0.9556', '0.854', '-0.2446', '-0.05313', '0.492', '0.6846', '-0.1349', '0.202', '0.1388', '-0.302', '-0.433', '0.2251', '-0.411', '-0.3486', '-0.1332', '-0.952', '0.4224', '0.15', '-0.06052', '-0.7964', '0.4546', '-0.4023', '-0.0763', '0.07764', '0.524', '-0.2676', '-0.1157', '-0.227', '-0.00232', '-0.3816', '-0.2354', '-0.11383', '-0.509', '0.3499', '-0.4634', '0.4512', '-0.459', '-0.292', '0.3186', '0.708', '-0.738', '0.3508', '-0.3035', '0.524', '-0.2349', '1.161', '-0.2308', '1.32', '0.3325', '-1.103', '-0.677', '0.683', '0.2339', '0.397', '-1.008', '-0.8154', '0.2294', '0.04416', '-0.768', '0.6216', '0.4473', '-0.03555', '-0.2178', '-0.0387', '0.552', '0.717', '-0.525', '0.1036', '-0.2988', '0.4216', '0.4275', '0.1097', '-0.3713', '-0.2216', '0.6', '-0.3667']",,,,,,,
mondo:0015338,syndromic craniosynostosis,"['syndromic craniosynostosis', 'syndrome associated with craniosynostosis']",,,139393,CN226660,"['0.3242', '0.05865', '-0.4546', '0.512', '0.3403', '-0.3752', '0.1979', '0.6987', '-1.1045', '-0.4746', '-0.013466', '-0.2544', '0.2644', '0.749', '-0.3684', '-0.347', '0.5845', '-0.3252', '0.02292', '-1.358', '-0.0634', '0.6504', '0.283', '-0.3848', '0.943', '0.6587', '-0.2847', '-0.11743', '0.4434', '0.7803', '-0.05353', '0.1688', '0.1865', '-0.404', '-0.3374', '0.3157', '-0.3748', '-0.2495', '-0.2208', '-0.9805', '0.3523', '0.1409', '-0.103', '-0.6313', '0.4192', '-0.4688', '0.14', '0.06885', '0.704', '-0.2068', '-0.03476', '-0.2355', '-0.1295', '-0.2632', '-0.1953', '-0.1406', '-0.4287', '0.2568', '-0.4653', '0.2856', '-0.5283', '-0.405', '0.2827', '0.5347', '-0.507', '0.4817', '-0.2426', '0.5747', '-0.2092', '1.139', '-0.1738', '1.313', '0.3303', '-0.956', '-0.3408', '0.7', '0.1857', '0.2966', '-1.035', '-0.6978', '0.1581', '0.12036', '-0.8013', '0.4263', '0.3293', '-0.0712', '-0.0765', '-0.1177', '0.4534', '0.7075', '-0.6587', '-0.04474', '-0.3647', '0.386', '0.3274', '0.1682', '-0.2961', '-0.09143', '0.673', '-0.4194']",,,,,,,
mondo:0015339,adrenomyeloneuropathy,"['AMN', 'adrenomyeloneuropathy']",,,139399,C1527231,"['-0.4453', '0.302', '0.0292', '-0.6797', '-0.0804', '0.2029', '-0.1818', '0.8', '-0.518', '-0.5327', '-0.0715', '-0.3022', '-0.1284', '0.2617', '0.583', '-0.7793', '-0.3743', '0.0001947', '-0.688', '-0.644', '-0.1073', '-0.4778', '0.2664', '-0.3694', '-0.04285', '-0.08777', '0.1993', '-0.0531', '-0.02556', '-0.5034', '0.349', '0.5063', '0.6084', '-0.406', '-0.1815', '0.05048', '-0.2133', '-0.3909', '-0.1521', '0.2272', '-0.0704', '-0.2754', '0.339', '-0.3699', '-0.2903', '0.06027', '-0.524', '-0.4902', '0.08093', '0.2788', '0.5234', '0.573', '-0.2812', '-0.2505', '-0.0899', '0.3691', '0.7324', '-0.5703', '-0.213', '0.2952', '0.4546', '0.4385', '0.481', '-0.02437', '-0.601', '0.3977', '-0.0443', '0.6763', '0.1552', '0.3857', '-0.0984', '-0.0479', '-0.4927', '-0.483', '0.871', '-0.06064', '-0.0784', '0.1132', '-0.2803', '-0.3523', '-0.2057', '-0.446', '0.0566', '0.4043', '-0.3262', '0.2462', '-0.012146', '-0.635', '0.7266', '-0.3398', '0.4543', '-0.1247', '0.0725', '0.1537', '0.367', '-0.2766', '0.2218', '0.1659', '-0.1414', '0.1704']",,,,,,,
mondo:0015340,drug rash with eosinophilia and systemic symptoms,"['drug reaction eosinophilic systemic syndrome', 'dress syndrome']",,,139402,,,,,,,,10058919,
mondo:0015341,congenital panfollicular nevus,"['congenital panfollicular nevus (disease)', 'congenital panfollicular nevus']",,,139414,,,,,,,,,0025471
mondo:0015342,acute transverse myelitis,,,,139417,C0270627,,C128378,,D009188,341.20,,,
mondo:0015343,secondary acute transverse myelitis,['disease-associated transverse myelitis'],,,139420,CN199396,,,,,,,,
mondo:0015344,idiopathic acute transverse myelitis,['ATM/TM'],,,139423,,,,,,,,,
mondo:0015345,perioral myoclonia with absences,['POMA'],,,139426,,,,,,,,,
mondo:0015346,Jeavons syndrome,"['epilepsy with eyelid myoclonias', 'eyelid myoclonia with and without absences', 'EMEA']",,,139431,CN199399,,,,,,,10084303,
mondo:0015347,multicentric reticulohistiocytosis,"['lipoid dermatoarthritis', 'giant cell histiocytomatosis', 'multicentric reticulohistiocytosis']",11824,,139436,C0311284,,C27896,,,713.0,,10070595,
mondo:0015348,leukoencephalopathy with bilateral anterior temporal lobe cysts,,,,139444,,,,,,,,,
mondo:0015349,progressive cavitating leukoencephalopathy,,,,139447,C4304840,,,,,,,,
mondo:0015350,17q11.2 microduplication syndrome,"['dup(17)(q11.2)', 'chromosome 17q11.2 duplication syndrome, 1.4-mb', 'trisomy 17q11.2', 'Grisart-Destrée syndrome', 'Nf1 Microduplication Syndrome', 'Grisart-Destree syndrome']",,618874,139474,CN199408,,,,,,,,
mondo:0015351,neuropathy with hearing impairment,,,,139512,CN199414,,,,,,,,
mondo:0015352,distal hereditary motor neuropathy type 2,"['dHMN2', 'dSMA2', 'distal spinal muscular atrophy type 2']",0111206,,139525,,"['-0.299', '0.1857', '0.1954', '-0.1337', '-0.0873', '-0.2502', '-0.1597', '0.405', '-0.417', '0.121', '0.001189', '-0.0694', '-0.05698', '0.01909', '0.1719', '0.002956', '0.08624', '-0.1322', '-0.1367', '-0.532', '0.299', '-0.2211', '0.07526', '0.2253', '0.1054', '0.03363', '0.02058', '-0.06445', '-0.441', '-0.0809', '0.1686', '0.06046', '0.38', '0.08154', '-0.07', '-0.2039', '-0.02194', '-0.2147', '-0.001215', '-0.2664', '-0.06866', '-0.1951', '-0.2734', '0.3276', '-0.1261', '-0.381', '0.0559', '0.2483', '0.05', '0.2795', '-0.03354', '0.2218', '-0.04636', '-0.11957', '-0.00892', '-0.205', '0.4216', '-0.1766', '-0.2302', '0.1163', '-0.06714', '0.03305', '0.04947', '0.1808', '-0.535', '0.15', '0.1902', '0.34', '-0.2123', '0.1741', '-0.251', '0.1963', '0.1761', '-0.4216', '0.3591', '0.1549', '0.1674', '0.2783', '-0.1748', '-0.1807', '0.033', '-0.1268', '0.354', '0.3423', '-0.2078', '-0.04022', '-0.1279', '0.1531', '0.1971', '0.0276', '0.1986', '0.08014', '0.166', '0.0651', '0.2815', '0.286', '0.342', '0.0143', '-0.01099', '0.3123']",,,C580044,,,,
mondo:0015353,"neuronopathy, distal hereditary motor, type 5A","['distal spinal muscular atrophy type 5', 'distal HMN V', 'neuronopathy, distal hereditary motor, type 5', 'dHMN5', 'distal hereditary motor neuropathy type V', 'spinal muscular atrophy, distal, type 5', 'spinal muscular atrophy, distal, with upper limb predominance', 'HMN5A', 'spinal muscular atrophy, distal, type 5A', 'HMN 5A', 'dHMN 5A', 'neuropathy, distal hereditary motor, type 5A', 'neuronopathy, distal hereditary motor, type VA', 'neuronopathy, distal hereditary motor, type 5A']",0111204,600794,,C1833308,,,,,,,,
mondo:0015354,hereditary sensory and autonomic neuropathy with deafness and global delay,['HSAN with deafness and global delay'],,,139573,CN226662,,,,,,,,
mondo:0015355,distal hereditary motor neuropathy type 7,"['distal spinal muscular atrophy with vocal cord paralysis', 'dHMN7']",0111199,,139589,CN199425,"['-0.08124', '0.2054', '0.136', '-0.4402', '-0.2961', '-0.4158', '0.2255', '0.3047', '-1.124', '-0.004562', '-0.1481', '-0.2869', '-0.4888', '0.2827', '0.7075', '-0.2301', '0.1912', '-0.2659', '0.1578', '-0.54', '0.0743', '-0.2864', '0.4368', '0.202', '-0.2488', '0.2673', '0.07324', '-0.1537', '-0.447', '0.1555', '-0.4443', '0.1707', '-0.01222', '-0.3064', '0.4785', '-0.2412', '-0.3245', '0.3733', '-0.2676', '-0.594', '-0.1324', '-0.543', '-0.0602', '0.271', '0.109', '-0.03995', '-0.1765', '0.177', '-0.004864', '0.3147', '-0.2344', '0.3044', '-0.1913', '0.002224', '-0.3442', '-0.659', '0.2377', '0.1508', '-0.0938', '0.081', '0.03049', '0.006424', '0.3464', '0.4907', '-0.5757', '0.1115', '0.1931', '0.5283', '-0.4453', '0.896', '-0.4138', '0.015274', '0.1218', '-0.04587', '0.432', '0.1707', '0.01863', '0.535', '-0.5986', '-0.2438', '-0.249', '-0.1742', '0.5273', '0.8916', '-0.4485', '-0.2329', '-0.3306', '0.363', '0.433', '-0.7246', '0.4673', '-0.1605', '0.2603', '0.3938', '0.506', '-0.3213', '0.695', '0.01241', '-0.07574', '0.3376']",,,,,,,
mondo:0015356,hereditary neoplastic syndrome,"['syndromes, hereditary neoplastic', 'familial tumor syndrome', 'familial neoplastic syndrome', 'hereditary tumor syndrome', 'inherited cancer syndrome', 'hereditary neoplastic syndromes', 'hereditary tumour syndrome', 'syndrome, hereditary cancer', 'hereditary neoplastic syndrome', 'syndrome, hereditary neoplastic', 'syndromes, hereditary cancer', 'cancer syndrome, hereditary', 'familial tumour syndrome', 'neoplastic syndrome, hereditary', 'inherited cancer-predisposing syndrome', 'hereditary cancer syndrome', 'cancer syndromes, hereditary', 'hereditary cancer syndromes']",,,140162,CN882908,,C3266,,D009386,,,,
mondo:0015357,secondary hypoparathyroidism due to impaired parathormon secretion,,,,140286,CN242104,,,,,,,,
mondo:0015358,hereditary motor and sensory neuropathy,['HMSN'],,,140450,,,,,D015417,,,,
mondo:0015359,autosomal dominant hereditary demyelinating motor and sensory neuropathy,,,,140453,CN228926,,,,,,,,
mondo:0015360,autosomal dominant hereditary axonal motor and sensory neuropathy,,,,140456,CN228927,,,,,,,,
mondo:0015361,autosomal recessive hereditary demyelinating motor and sensory neuropathy,,,,140459,CN228928,,,,,,,,
mondo:0015362,autosomal dominant distal hereditary motor neuropathy,"['autosomal dominant distal hereditary motor neuropathy', 'autosomal dominant dHMN', 'distal hereditary motor neuropathy, autosomal dominant', 'autosomal dominant distal spinal muscular atrophy']",0111198,,140465,CN228930,"['-0.02518', '0.1356', '0.12494', '-0.0827', '-0.01504', '-0.2673', '-0.1161', '0.2917', '-0.2732', '0.04962', '-0.0375', '-0.00817', '-0.0859', '0.00391', '0.1602', '-0.03348', '-0.009094', '-0.1132', '0.0125', '-0.4275', '0.0193', '-0.0882', '0.00805', '0.219', '0.04953', '0.06885', '-0.0795', '-0.03464', '-0.05228', '-0.2495', '0.0653', '0.03012', '0.1335', '-0.003914', '-0.00712', '-0.2069', '-0.0347', '-0.1711', '-0.0392', '-0.1615', '-0.0882', '-0.3215', '0.03864', '0.1567', '-0.04114', '-0.3408', '-0.10974', '0.1969', '0.06183', '0.06903', '0.002422', '0.0755', '-0.1225', '-0.09467', '-0.004612', '-0.2412', '0.2517', '-0.0218', '-0.2607', '-0.02194', '0.11127', '-0.06573', '0.2019', '0.12024', '-0.10297', '0.1165', '0.1539', '0.3809', '-0.1406', '0.1932', '-0.1681', '-0.04565', '0.09735', '-0.2003', '0.3464', '0.1941', '-0.06015', '0.07996', '-0.12256', '-0.1384', '-0.09424', '-0.09296', '0.08887', '0.3865', '-0.06177', '0.09143', '-0.004734', '0.11993', '0.082', '0.02295', '0.1439', '0.0972', '0.1498', '0.06046', '0.415', '0.1437', '0.2917', '-0.1649', '-0.1105', '0.1294']",,,,,,,
mondo:0015363,autosomal recessive distal hereditary motor neuropathy,"['autosomal recessive distal spinal muscular atrophy', 'autosomal recessive dHMN', 'autosomal recessive dSMA', 'distal hereditary motor neuropathy, autosomal recessive']",0111197,,140468,CN228931,,,,,,,,
mondo:0015364,hereditary sensory and autonomic neuropathy,"['congenital pain insensitivity', 'hereditary sensory and autonomic neuropathy', 'HSAN', 'hereditary sensory autonomic neuropathy', 'hereditary sensory neuropathy', 'hereditary sensory peripheral neuropathy', 'congenital insensitivity to pain', 'indifference to pain, Congenital, autosomal recessive', 'CIP']",0050548,,140471,C0027889,,C125386,,D009477,356.2,,,
mondo:0015365,autosomal dominant hereditary sensory and autonomic neuropathy,"['hereditary sensory and autonomic neuropathy, autosomal dominant']",,,140474,CN228932,"['1.017', '0.00752', '-0.501', '0.4937', '-0.4097', '-0.5347', '-0.2211', '0.312', '-0.6924', '0.2021', '0.2218', '0.569', '0.1315', '0.7627', '-0.762', '0.2576', '-0.06915', '0.86', '-0.74', '-0.77', '0.1699', '-0.0333', '-0.852', '0.398', '0.0838', '-0.199', '-0.666', '0.02312', '0.04614', '-0.3', '0.7925', '0.01204', '0.5337', '-0.2905', '-0.438', '-0.2947', '-0.00843', '0.2585', '0.14', '-0.4368', '-0.5356', '-0.03104', '0.004547', '-0.2189', '0.2925', '-0.537', '0.3577', '-0.1567', '0.547', '0.0263', '-0.3455', '0.9995', '0.3638', '-0.9414', '-0.12476', '0.606', '0.6104', '0.2412', '-0.5903', '-0.5986', '0.1837', '0.638', '0.2754', '0.3223', '-0.2273', '0.855', '0.3726', '0.5347', '-0.0376', '0.4072', '-0.717', '0.4587', '-0.3853', '-0.2756', '0.7607', '0.2382', '0.11194', '0.964', '-0.5967', '0.3584', '-0.0374', '-0.7603', '0.3604', '0.3293', '0.2078', '0.03598', '0.5674', '-0.1222', '0.6577', '-0.3948', '0.1747', '-0.1338', '0.638', '-0.04248', '1.195', '1.105', '-0.6274', '-0.2015', '0.1056', '0.2297']",,,,,,,
mondo:0015366,autosomal recessive hereditary sensory and autonomic neuropathy,"['hereditary sensory and autonomic neuropathy, autosomal recessive']",,,140477,CN228933,"['1.022', '-0.01072', '-0.4875', '0.6284', '-0.3406', '-0.635', '-0.2676', '0.3074', '-0.5757', '0.33', '-0.01027', '0.617', '0.11804', '0.8716', '-0.756', '0.1874', '-0.0935', '0.8687', '-0.8135', '-0.7017', '0.2507', '-0.03357', '-0.8164', '0.4429', '0.2277', '-0.1251', '-0.656', '0.0282', '0.013596', '-0.2092', '0.8325', '0.11365', '0.5605', '-0.2411', '-0.439', '-0.2427', '-0.05072', '0.1442', '0.1669', '-0.4905', '-0.727', '0.014626', '0.02399', '-0.143', '0.333', '-0.452', '0.4368', '-0.1494', '0.511', '0.165', '-0.4294', '0.976', '0.3782', '-0.9365', '-0.06555', '0.6265', '0.5674', '0.3296', '-0.574', '-0.5493', '0.2158', '0.6577', '0.2993', '0.1954', '-0.132', '0.83', '0.3545', '0.4336', '-0.015396', '0.4697', '-0.6934', '0.4226', '-0.4377', '-0.2317', '0.6333', '0.1907', '0.0702', '1.021', '-0.643', '0.3567', '-0.006474', '-0.7275', '0.287', '0.3743', '0.152', '0.0352', '0.4631', '-0.10406', '0.703', '-0.4163', '0.2827', '-0.0826', '0.6797', '-0.1926', '1.168', '1.07', '-0.5327', '-0.1538', '0.03622', '0.27']",,,,,,,
mondo:0015367,Charlie M syndrome,,,,1406,CN199458,,,,,,,,
mondo:0015368,neuro-ophthalmological disease,,,,183616,CN199459,,,,,,,,
mondo:0015369,Joubert syndrome and related disorders,['JSRD'],,,140874,CN199461,,,,,,,,
mondo:0015371,linear atrophoderma of Moulin,,,,140933,C1274753,,,,,,,,
mondo:0015372,autosomal dominant macrothrombocytopenia,,,,140957,CN199474,,,,,,,,
mondo:0015374,primary central nervous system vasculitis,"['granulomatous angiitis of the central nervous system', 'primary CNS vasculitis', 'primary vasculitis of the central nervous system', 'primary central nervous system vasculitis', 'primary angiitis of the central nervous system', 'PACNS', 'isolated angiitis of the central nervous system', 'PCNSV']",,,140989,,,,,D020293,,,,
mondo:0015375,orofaciodigital syndrome,"['oral-facial-digital syndrome', 'orofaciodigital syndromes', 'orofaciodigital syndrome', 'OFD', 'oral-facial-digital syndromes', 'oral facial digital syndromes']",4501,,140997,,"['0.09894', '0.18', '0.1505', '-0.285', '0.3145', '-0.3748', '-0.2268', '0.2004', '-0.351', '-0.2524', '-0.04004', '-0.1824', '0.1464', '-0.0727', '-0.1614', '0.0988', '0.04755', '-0.02812', '-0.2069', '-0.3699', '-0.1394', '-0.03522', '0.4111', '-0.217', '0.1494', '0.2009', '-0.2676', '-0.1638', '0.3184', '-0.2306', '0.2969', '0.004555', '0.0648', '-0.11926', '0.0929', '-0.1653', '0.1048', '-0.3599', '-0.1663', '-0.3867', '0.0606', '-0.3345', '0.10156', '-0.0634', '0.2211', '-0.4763', '-0.1571', '0.2144', '0.11304', '-0.123', '-0.08655', '-0.11835', '-0.01433', '-0.1661', '-0.09216', '-0.1935', '0.3994', '0.1582', '-0.3867', '0.2139', '0.01619', '-0.04898', '0.1357', '0.2188', '-0.02377', '-0.0846', '0.0622', '-0.05127', '-0.26', '0.26', '-0.5903', '-0.1484', '0.0784', '0.1678', '0.4087', '0.2573', '-0.053', '0.05966', '-0.2386', '-0.148', '-0.05295', '0.2454', '0.1481', '0.0121', '0.00203', '0.0421', '0.064', '0.4182', '0.02489', '0.077', '-0.177', '0.443', '0.3772', '-0.0478', '0.5806', '0.0786', '0.292', '-0.556', '0.2129', '-0.01427']",,,D009958,759.89,,,
mondo:0015376,first branchial cleft anomaly,"['first branchial cleft fistula', 'first branchial cleft cyst']",,,141013,,,,,,,,,
mondo:0015377,third branchial cleft anomaly,"['third branchial cleft fistula', 'third branchial cleft cyst']",,,141030,,,,,,,,,
mondo:0015378,fourth branchial cleft anomaly,"['fourth branchial cleft cyst', 'fourth branchial cleft fistula']",,,141037,,,,,,,,,
mondo:0015379,cervical dermoid cyst,['dermoid cyst of the neck'],,,141046,,,,,,,,,
mondo:0015380,facial dermoid cyst,['dermoid cyst of the face'],,,141051,,,,,,,,,
mondo:0015381,commissural lip fistula,"['cysts and fistulae of the face and oral cavity of labial commissure', 'labial commissure cysts and fistulae of the face and oral cavity']",,,141061,,,,,,,,,
mondo:0015382,lower lip fistula,"['lower lip cysts and fistulae of the face and oral cavity', 'cysts and fistulae of the face and oral cavity of lower lip']",,,141064,,,,,,,,,
mondo:0015383,cervicofacial fibrochondroma,['cervicofacial enchondroma'],,,141067,,,,,,,,,
mondo:0015384,digestive duplication cyst of the tongue,"['gastric duplication cyst of the tongue', 'cysts and fistulae of the face and oral cavity of tongue', 'foregut duplication cyst of the tongue', 'enteric duplication cyst of the tongue', 'tongue cysts and fistulae of the face and oral cavity']",,,141071,,,,,,,,,
mondo:0015385,external auditory canal aplasia/hypoplasia,['external auditory canal stenosis/atresia'],,,141074,,,,,,,,,
mondo:0015386,epignathus,"['epignathus (disease)', 'oropharyngeal teratoma', 'Epignathus']",,,141077,C0266725,,,,,,,,0030767
mondo:0015387,nasolacrimal duct cyst,"['dacryocystocele', 'nasolacrimal mucocele', 'dacryocele']",,,141083,,,,,,,,,
mondo:0015388,polyrrhinia,"['Polyrhinia', 'Double nose']",,,141091,,,,,,,,,
mondo:0015389,supernumerary nostril,"['accessory nostril', 'supernumerary naris']",,,141096,CN226671,,,,,,,,0009934
mondo:0015390,proboscis lateralis,['congenital tubular nose'],,,141099,C4274985,,,,,,,,
mondo:0015391,nasopharyngeal teratoma,"['teratoma of the nasopharynx', 'nasopharynx teratoma']",,,141107,C4531264,,,,,,D10.6,,
mondo:0015392,nasal glial heterotopia,['nasal glioma'],,,141112,C0266490,,,,,748.1,,,
mondo:0015393,nasal ganglioglioma,,,,141115,,,,,,,,,
mondo:0015394,nasal encephalocele,,,,141118,,,,,,,,,
mondo:0015395,congenital subglottic stenosis,,,,141121,,,,,,748.3,Q31.1,,
mondo:0015396,congenital laryngeal cyst,,,,141124,C0339880,,,,,,,,
mondo:0015397,oculo-auriculo-vertebral spectrum,"['OAV spectrum', 'Goldenhar syndrome', 'craniofacial microsomia', 'oculoauriculovertebral syndrome', 'first and second branchial arch syndrome', 'unilateral or bilateral and asymmetric otomandibular dysplasia', 'Goldenhar disease', 'OAV dysplasia', 'hemifacial microsomia', 'HFM', 'Expanded spectrum of hemifacial microsomia', 'facio-auriculo-vertebral spectrum', 'oculoauriculovertebral spectrum', 'first arch syndrome', 'oculoauriculovertebral dysplasia', 'OAV (oculoauriculovertebral) dysplasia', 'Expanded spectrum hemifacial microsomia', 'oculo-auriculo-vertebral dysplasia', 'facioauriculovertebral sequence', 'Fav sequence', 'facioauriculovertebral dysplasia', 'OAVS', 'OAVD']",2907,164210,374,C0265240,,C84740,,D006053,759.89,,,
mondo:0015398,hemifacial microsomia,"['otomandibular dysostosis', 'first branchial arch syndrome', 'Laterofacial microsomia', 'otomandibular syndrome']",,,141136,CN199493,,,,,,,,
mondo:0015399,glossopalatine ankylosis,['Cosack syndrome'],,,141163,CN199497,,,,,,,,
mondo:0015400,frontonasal arteriovenous malformation,,,,141168,,,,,,,,,
mondo:0015401,maxillary arteriovenous malformation,['arteriovenous malformation of maxilla'],,,141171,,,,,,,,,
mondo:0015402,mandibular arteriovenous malformation,['arteriovenous malformation of mandible'],,,141174,,,,,,,,,
mondo:0015403,non-involuting congenital hemangioma,"['noninvoluting congenital hemangioma', 'NICH']",,,141179,C1275417,,C172208,,,,,,
mondo:0015404,rapidly involuting congenital hemangioma,['rich'],0080895,,141184,C1275421,,C172207,,,,,,
mondo:0015405,cerebrofacial arteriovenous metameric syndrome,['CAMS'],,,141189,CN199500,,,,,,,,
mondo:0015406,cerebrofacial arteriovenous metameric syndrome type 1,['CAMS1'],,,141194,CN199501,,,,,,,,
mondo:0015407,cerebrofacial arteriovenous metameric syndrome type 3,['CAMS3'],,,141199,CN199502,,,,,,,,
mondo:0015408,diffuse lymphatic malformation,"['Gla', 'generalized lymphatic anomaly', 'disseminated lymphangiomatosis', 'diffuse lymphangioma', 'diffuse lymphangiomatosis', 'disseminated lymphangioma', 'generalised lymphatic anomaly', 'disseminated lymphatic malformation']",0081031,,141209,C0343090,,,,,,,,
mondo:0015409,isolated congenital syngnathia,['isolated congenital maxillomandibular fusion'],,,141214,,,,,,,,,
mondo:0015410,nasal dorsum fistula/cyst,,,,141219,,,,,,,,,
mondo:0015411,facial cleft,"['craniofacial cleft', 'prosoposchisis', 'cleft face']",,,141229,,,C124510,,,,,,
mondo:0015412,median facial cleft,"['Tessier number 0-14 and 30 facial cleft', 'Midline facial cleft']",,,141234,,,,,,,,,
mondo:0015413,median cleft of the upper lip and maxilla,,,,141239,,,,,,,,,
mondo:0015414,paramedian nasal cleft,"['alar cleft', 'isolated cleft of the ala nasi', 'isolated coloboma of the nose', 'Tessier number 1 cleft', 'alar rim cleft', 'cleft nose']",,,141242,,,,,,748.1,,,
mondo:0015415,oblique facial cleft,['Orbitofacial cleft'],,,141253,,,,,,,,,
mondo:0015416,Tessier number 5 facial cleft,,,,141261,,,,,,,,,
mondo:0015417,Tessier number 6 facial cleft,,,,141265,,,,,,,,,
mondo:0015418,lateral facial cleft,"['Tessier number 7 facial cleft', 'transverse facial cleft']",,,141269,,,,,,,,,
mondo:0015419,midline cervical cleft,,,,141288,,,,,,744.89,,,
mondo:0015420,cleft lip and alveolus,,,,141291,,,,,,525.8,,,
mondo:0015421,orofaciodigital syndrome type 12,"['OFDS 12', 'OFD12', 'Moran-Barroso syndrome', 'oral-facial-digital syndrome 12', 'oral-facial-digital syndrome type 12', 'oral facial digital syndrome 12', 'orofaciodigital syndrome 12', 'orofaciodigital syndrome XII', 'oral facial digital syndrome type 12']",,,141327,C2932679,,,,C548034,,,,
mondo:0015422,orofaciodigital syndrome type 13,"['oral facial digital syndrome 13', 'Degner syndrome', 'oral-facial-digital syndrome type 13', 'OFD13', 'oral-facial-digital syndrome 13', 'OFDS 13', 'orofaciodigital syndrome XIII', 'oral-facial-digital syndrome XIII', 'oral facial digital syndrome type 13', 'orofaciodigital syndrome 13', 'OFD syndrome 13']",,,141330,C2932680,,,,C548035,,,,
mondo:0015424,"lethal chondrodysplasia, Moerman type","['lethal chondrodysplasia Moerman type', 'Moerman-Vandenberghe-Fryns syndrome']",,,1420,CN199519,,,,,,,,
mondo:0015425,lethal recessive chondrodysplasia,"['Maroteaux-Stanescu-Cousin syndrome', 'chondrodysplasia lethal recessive']",,,1423,CN199522,,,,,,,,
mondo:0015426,Desbuquois dysplasia,"['micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification', 'DBQD', 'desbuquois syndrome', 'micromelic dwarfism, narrow chest, vertebral and metaphyseal abnormalities and advanced carpotarsal ossification', 'Desbuquois dysplasia']",0060462,,1425,CN239270,"['-0.537', '-0.4458', '0.4272', '0.1896', '0.562', '-0.3755', '-0.1168', '1.312', '-0.576', '-0.1671', '-0.2778', '0.0309', '0.0977', '0.00906', '-0.4253', '-0.3523', '-0.05838', '0.03415', '-0.3467', '-0.599', '-0.0623', '0.05756', '0.892', '-0.05728', '-0.1937', '0.4814', '-0.2605', '0.3188', '0.621', '-0.4739', '0.271', '-0.406', '0.2686', '0.06464', '0.496', '0.1688', '-0.63', '-0.8965', '-0.4602', '-0.4294', '0.809', '-0.7954', '0.3352', '-0.003944', '0.3965', '0.1954', '-0.2864', '0.9175', '-0.0996', '-0.0847', '0.2861', '-0.5557', '-0.403', '0.1879', '-0.2937', '-1.2295', '0.1239', '-0.1494', '-0.0639', '-0.3833', '0.1511', '-0.3582', '-0.6626', '0.05634', '-0.639', '0.0849', '-0.2241', '-0.4084', '-0.1008', '0.6064', '-0.2937', '-0.3113', '0.02048', '-0.468', '-0.09686', '0.3835', '-0.441', '0.2257', '-0.8804', '0.2722', '0.2068', '-0.1372', '0.2827', '0.647', '-0.2925', '0.2455', '0.8794', '1.405', '0.06696', '0.2957', '-0.3208', '0.5234', '0.4026', '-0.3657', '0.7803', '-0.45', '-0.1007', '-0.629', '0.1355', '-0.03992']",C124056,,,756.9,,,
mondo:0015427,paroxysmal dyskinesia,"['paroxysmal dystonic choreoathetosis', 'paroxysmal choreoathetosis']",,,1431,,,,,D002819,333.5,,,
mondo:0015428,choroidal atrophy-alopecia syndrome,"['regional choroidal atrophy and alopecia', 'choroidal atrophy alopecia', 'fine hair, absent/decreased lashes, absent/decreased eyebrows, visual loss-mild/suspected, dysplastic/thick/grooved toenails and fingernails', 'Moloney syndrome']",,,1433,C2931026,,,,C535810,,,,
mondo:0015429,choroideremia-hypopituitarism syndrome,['CHM-hypopituitarism syndrome'],,,1434,CN226680,,,,,,,,
mondo:0015430,ring chromosome 1,"['Ring 1', 'chromosome 1, ring', 'chromosome 1 ring', 'R1', 'Ring chromosome type 1', 'Ring chromosome 1 syndrome', 'r(1) syndrome']",,,1437,CN036412,,C36474,,C535361,,,,
mondo:0015431,ring chromosome 10,"['Ring chromosome type 10', 'r10', 'Ring chromosome 10 syndrome', 'chromosome 10 ring', 'Ring 10']",,,1438,CN037257,,,,C538086,,,,
mondo:0015432,ring chromosome 12,"['Ring chromosome 12 syndrome', 'Ring chromosome type 12', 'Ring 12', 'R12', 'chromosome 12 ring']",,,1439,C0795843,,,,C538298,,,,
mondo:0015433,ring chromosome 17,"['Ring chromosome 17 syndrome', 'Ring 17', 'Ring chromosome type 17', 'R17', 'chromosome 17 ring']",,,1441,,,,,C538046,,,,
mondo:0015434,ring chromosome 18,"['Ring chromosome type 18', 'Ring chromosome 18 syndrome', 'Ring 18', 'chromosome 18 ring', 'R18']",,,1442,C0265475,,,0001226,C538304,,,,
mondo:0015435,ring chromosome 19,"['Ring chromosome 19 syndrome', 'chromosome 19 ring', 'R19', 'Ring 19', 'Ring chromosome type 19']",,,1443,CN036553,,,,C538310,,,,
mondo:0015436,ring chromosome 20,"['Ring 20', 'chromosome 20 ring', 'Ring chromosome 20 syndrome', 'Ring chromosome type 20', 'R20']",,,1444,,,C169001,,C580424,758.89,,,
mondo:0015437,ring chromosome 21,"['chromosome 21 en anneau', 'Ring chromosome 21 syndrome', 'Ring chromosome type 21', 'R21', 'chromosome 21 ring', 'Ring 21']",,,1445,CN037252,,,,C537109,,,,
mondo:0015438,ring chromosome 22,"['Ring 22', 'chromosome 22 ring', 'R22', 'Ring chromosome type 22', 'Ring chromosome 22 syndrome', 'r(22) syndrome']",,,1446,CN036599,,,,C536795,,,,
mondo:0015439,ring chromosome 4,"['Ring chromosome type 4', 'rose cluster 4', 'Ring chromosome 4 syndrome', 'r(4) syndrome', 'R4', 'chromosome 4 ring', 'syndrome r(4)', 'Ring 4']",,,1447,,,C121983,,C537636,,,,
mondo:0015440,ring chromosome 6,"['R6', 'rose cluster 6', 'chromosome 6 ring', 'Ring chromosome type 6', 'Ring chromosome 6 syndrome', 'Ring 6']",,,1448,,,C121985,,C537763,,,,
mondo:0015441,ring chromosome 7,"['rose cluster 7', 'chromosome 7 ring', 'Ring chromosome 7 syndrome', 'R7', 'Ring 7', 'Ring chromosome type 7']",,,1449,,,C121986,,C537813,,,,
mondo:0015443,chromosome 8-derived supernumerary ring/marker,"['R8', 'ring chromosome 8', 'Ring chromosome 8 syndrome', 'r(8) syndrome', 'rose cluster 8', 'chromosome 8 ring', 'Ring 8', 'supernumerary ring/marker 8']",,,1450,CN036129,,C121988,,C537824,,,,
mondo:0015445,autosomal dominant coarctation of aorta,"['autosomal dominant aorta coarctation', 'aorta coarctation, autosomal dominant']",,,1455,,,,,,,,,
mondo:0015446,atypical coarctation of aorta,"['middle aortic syndrome', 'coarctation of the abdominal aorta', 'mid-aortic syndrome', 'Midaortic syndrome', 'mid-aortic dysplastic syndrome']",,,1456,C3805239,,,,,,,,
mondo:0015447,differentiated thyroid carcinoma,"['differentiated thyroid gland carcinoma', 'papillary or follicular thyroid carcinoma', 'well-differentiated thyroid cancer', 'thyroid gland well differentiated carcinoma', 'well-differentiated thyroid carcinoma', 'well differentiated thyroid carcinoma', 'differentiated thyroid cancer', 'differentiated thyroid gland cancer', 'differentiated thyroid carcinoma', 'thyroid gland differentiated carcinoma', 'well differentiated thyroid gland carcinoma']",0080525,,146,C1337013,,C7153,1002017,,,,,
mondo:0015448,mitochondrial complex III deficiency,"['isolated CoQ-cytochrome C reductase deficiency', 'isolated mitochondrial respiratory chain complex III deficiency', 'isolated coenzyme Q-cytochrome C reductase deficiency', 'isolated complex III deficiency', 'isolated ubiquinone-cytochrome C reductase deficiency']",0111139,,1460,,"['-0.378', '0.171', '-0.03296', '-0.0477', '0.0787', '-0.2308', '0.1323', '0.2339', '-0.11414', '0.2068', '-0.1802', '-0.287', '0.10425', '-0.03482', '-0.10565', '-0.06396', '-0.0432', '-0.2094', '-0.2812', '-0.58', '0.03105', '-0.1293', '0.5073', '0.02222', '0.0967', '-0.08875', '0.03394', '0.1346', '0.05176', '-0.267', '0.258', '0.3503', '0.5356', '0.369', '-0.1311', '-0.4075', '-0.3062', '-0.1046', '-0.376', '0.01377', '-0.07526', '-0.2515', '0.1371', '0.1345', '-0.2079', '-0.2659', '0.04016', '0.0813', '-0.1969', '0.1749', '-0.3105', '0.09644', '-0.004986', '-0.1652', '-0.04343', '-0.2437', '0.0878', '-0.1304', '-0.1849', '0.3093', '0.1271', '-0.09064', '0.3896', '-0.159', '-0.1581', '0.06665', '0.3923', '0.4578', '-0.38', '0.1467', '-0.362', '0.07196', '0.0942', '0.036', '0.01628', '0.1316', '0.3608', '-0.2798', '0.0865', '0.2017', '0.1309', '-0.02303', '-0.1731', '0.1621', '0.3586', '0.1879', '0.1159', '0.1589', '0.4907', '0.11163', '0.384', '0.328', '-0.07135', '-0.05945', '0.447', '0.354', '0.3228', '-0.1735', '0.2595', '0.1676']",,,,,,,
mondo:0015449,criss-cross heart,"['twisted atrioventricular connections', 'criss-cross atrioventricular relationships', 'superoinferior ventricles']",,,1461,,,,,D003420,746.89,,,
mondo:0015450,triatrial heart,['Cor triatriatum'],,,1463,,,C84651,,,746.82,,,
mondo:0015451,univentricular heart,['Double inlet left ventricle'],,,1464,,,,,D000080039,746.89,,10045545,
mondo:0015452,Coffin-Siris syndrome,"['short stature-onychodysplasia.', 'dwarfism-onychodysplasia', 'intellectual disability with absent fifth fingernail and terminal phalanx', 'CSS', 'fifth digit syndrome']",1925,,1465,C0265338,,C35321,,C536436,759.89,,,
mondo:0015453,Cogan syndrome,"['Cogan syndrome', 'diffuse interstitual keratitis', 'Cogan^s syndrome']",0060216,,1467,CN199560,,,,D055952,,,10056667,
mondo:0015454,multiple carboxylase deficiency,"['MCD', 'multiple carboxylase deficiency']",857,,148,C0026755,,,,D009100,,D81.819,10028176,
mondo:0015455,gonococcal conjunctivitis,"['gonococcal ophthalmia neonatorum', 'conjunctivitis gonococcal']",,,1482,,,C116816,,,,A54.31,,
mondo:0015457,corpus callosum agenesis-double urinary collecting system syndrome,"['Ben Ari Shuper Mimouni syndrome', 'corpus callosum agenesis-double urinary collecting system syndrome', 'corpus callosum agenesis double urinary collecting', 'corpus callosum agenesis - double urinary collecting system', 'Ben Ari-Shuper-Mimouni syndrome', 'agenesis of corpus callosum with double urinary collecting system, trigonocephaly and minor anomalies']",,,1492,C2930897,,,,C535427,,,,
mondo:0015458,intellectual disability-hypoplastic corpus callosum-preauricular tag syndrome,"['intellectual disability - hypoplastic corpus callosum - preauricular tag', 'Da Silva syndrome']",,,1495,CN199578,,,,,,,,
mondo:0015459,nasopharyngeal carcinoma,"['malignant neoplasm of nasopharyngeal wall', 'cancer of the nasopharynx', 'malignant neoplasm of lateral wall of nasopharynx', 'nasopharyngeal carcinoma', 'squamous cell carcinoma of the nasopharynx', 'malignant tumor of anterior wall of nasopharynx', 'nasopharynx carcinoma', 'malignant neoplasm of nasopharynx (disorder) [ambiguous]', 'malignant tumor of posterior wall of nasopharynx', 'carcinoma of the nasopharynx', 'malignant nasopharyngeal tumour', 'cancer of nasopharynx', 'malignant neoplasm of anterior wall of nasopharynx', 'malignant tumour of anterior wall of nasopharynx', 'malignant neoplasm of other specified sites of nasopharynx', 'nasopharyngeal throat cancer', 'malignant neoplasm of nasopharynx', 'malignant tumour of lateral wall of nasopharynx', 'malignant neoplasm of posterior wall of nasopharynx', 'malignant nasopharyngeal tumor', 'carcinoma of nasopharynx', 'NPC', 'malignant neoplasm of roof of nasopharynx', 'malignant tumour of posterior wall of nasopharynx', 'primary malignant neoplasm of anterior wall of nasopharynx', 'malignant tumor of lateral wall of nasopharynx', 'malignant neoplasm of superior wall of nasopharynx', 'nasopharyngeal cancer']",9261,,150,CN199582,,C3871,,D000077274,147.9,,10028793,
mondo:0015461,short rib-polydactyly syndrome,,,,1505,C0036996,"['-0.03696', '0.0441', '0.2898', '0.2961', '0.3354', '-0.276', '0.03732', '0.1925', '-0.3562', '-0.4404', '-0.214', '-0.1219', '0.1292', '0.1783', '0.01537', '0.0546', '0.1003', '-0.433', '0.1216', '-0.546', '0.1179', '0.3635', '1.082', '-0.112', '0.1542', '0.132', '-0.343', '0.1118', '0.443', '-0.10376', '0.0835', '0.0169', '0.05978', '0.17', '0.2683', '-0.3674', '-0.2903', '-0.2764', '-0.08276', '0.02061', '0.3982', '-0.105', '-0.0803', '-0.0695', '0.315', '-0.2496', '0.1431', '0.9995', '0.2651', '-0.1071', '0.0126', '-0.3708', '0.234', '-0.0919', '-0.6714', '-0.8657', '-0.613', '0.3113', '-0.1638', '0.2311', '0.2262', '0.0921', '0.07935', '-0.00735', '-0.2012', '-0.3042', '0.1702', '-0.09875', '-0.518', '0.3196', '-0.1525', '0.11224', '0.525', '-0.1481', '0.3276', '0.1672', '-0.2642', '-0.05502', '-0.607', '-0.647', '-0.1122', '0.01126', '0.0896', '-0.1395', '-0.02867', '-0.0977', '0.4248', '0.1143', '0.1984', '-0.1022', '-0.0595', '0.1177', '0.3337', '-0.2043', '0.2444', '0.2769', '0.6133', '-0.4458', '-0.02216', '0.362']",C85065,,D012779,756.3,,,
mondo:0015462,thin ribs-tubular bones-dysmorphism syndrome,['Sharma-Kapoor-Ramji syndrome'],,,1506,C2931543,,,,C537595,,,,
mondo:0015463,craniodigital syndrome-intellectual disability syndrome,"['craniodigital syndrome with mental retardation', 'Scott craniodigital syndrome with mental retardation', 'Scott craniodigital syndrome with intellectual disability', 'craniodigital syndrome-mental retardation, Scott type', 'craniodigital syndrome-intellectual disability, Scott type', 'Scott Bryant Graham syndrome', 'Scott craniodigital syndrome', 'Scott-Bryant-Graham syndrome', 'craniodigital syndrome with intellectual disability', 'craniodigital-intellectual disability syndrome']",,312860,1514,C1839311,,,,C537528,,,,
mondo:0015464,craniofrontonasal dysplasia-Poland anomaly syndrome,['Webster-Deming syndrome'],,,1521,CN199598,,,,,,,,
mondo:0015465,craniometaphyseal dysplasia,,0080033,,1522,,"['-0.4956', '0.245', '0.3433', '-0.04355', '0.0946', '-0.1438', '0.0431', '0.3281', '-0.3115', '0.001734', '-0.04544', '0.0431', '0.0388', '0.06256', '-0.02942', '-0.122', '0.2036', '0.03137', '-0.1483', '-0.4817', '0.01694', '-0.001512', '0.4302', '-0.1912', '0.014015', '0.1451', '-0.01322', '-0.1862', '0.1283', '0.02783', '0.02226', '0.02898', '0.11383', '0.1022', '0.1354', '-0.1503', '-0.0555', '-0.2244', '0.0409', '-0.313', '0.09424', '-0.2386', '0.0743', '-0.2788', '-0.0787', '-0.252', '-0.1699', '0.2634', '0.1537', '-0.096', '0.04794', '0.01086', '0.2279', '0.1594', '-0.349', '-0.4019', '-0.10547', '0.003746', '-0.10895', '-0.0203', '0.3484', '0.09595', '-0.2874', '-0.09436', '-0.05743', '-0.1632', '0.2126', '0.2383', '-0.2065', '0.25', '-0.1477', '-0.1575', '0.2435', '-0.1184', '-0.1953', '0.0859', '0.044', '0.1062', '-0.04382', '-0.1724', '-0.11865', '-0.0655', '-0.0655', '0.3452', '-0.2168', '0.0976', '-0.0683', '0.283', '0.2925', '0.01775', '-0.01498', '0.0865', '-0.01604', '0.196', '0.444', '0.04926', '0.501', '-0.3665', '0.2242', '0.1665']",,,,756.89,,,
mondo:0015466,cranio-osteoarthropathy,"['cranio osteoarthropathy', 'Currarino idiopathic osteoarthropathy', 'Currarino disease', 'Reginato-Schiapachasse syndrome']",,,1525,CN199601,,,,,,,,
mondo:0015467,"craniosynostosis, Philadelphia type",,,,1527,,,,,C563368,,,,
mondo:0015468,craniosynostosis-cataract syndrome,,,,1530,CN226684,,,,,,,,
mondo:0015469,craniosynostosis,"['CSO', 'premature closure of cranial sutures', 'craniosynostosis syndrome']",2340,,1531,C0010278,"['0.1117', '-0.12054', '-0.0719', '0.3596', '0.328', '-0.2488', '0.02173', '0.4722', '-1.051', '-0.4382', '0.04813', '-0.00563', '0.3376', '0.9707', '-0.03137', '-0.2499', '0.4531', '-0.5356', '-0.0908', '-1.008', '0.0561', '0.746', '0.566', '-0.4604', '0.956', '0.688', '-0.05682', '-0.2961', '0.3887', '0.658', '-0.1667', '0.3406', '0.02261', '-0.2761', '-0.3745', '0.07446', '-0.4077', '-0.569', '-0.2634', '-1.002', '0.4075', '0.1798', '-0.1466', '-0.7324', '0.2032', '-0.6104', '0.2274', '0.1985', '0.4302', '-0.1312', '0.05228', '-0.623', '0.01323', '-0.3616', '-0.514', '-0.2605', '-0.436', '0.4307', '-0.4758', '0.553', '-0.4683', '-0.2825', '0.03247', '0.405', '-0.5464', '0.293', '-0.0971', '0.3938', '-0.258', '0.939', '-0.1833', '1.075', '0.4744', '-0.927', '-0.587', '0.77', '0.4565', '0.3413', '-0.9854', '-0.933', '0.3047', '0.0911', '-0.733', '0.4688', '0.2878', '-0.10144', '-0.05948', '-0.3135', '0.5947', '0.472', '-0.404', '-0.1346', '-0.1257', '0.4292', '0.3965', '0.0765', '-0.08527', '-0.2605', '0.786', '-0.3125']",C84655,,D003398,,Q75.0,10049889,
mondo:0015470,familial isolated dilated cardiomyopathy,['familial or idiopathic dilated cardiomyopathy'],,,154,CN199609,,,,,,,,
mondo:0015471,benign focal seizures of adolescence,['adolescent benign focal crisis'],,,1544,C4275141,,,,,,,,
mondo:0015473,cryptorchidism-arachnodactyly-intellectual disability syndrome,"['cryptorchidism arachnodactyly intellectual deficit', 'Van Benthem-Driessen-Hanveld syndrome']",,,1548,CN199616,,,,,,,,
mondo:0015474,cryptosporidiosis,"['infection by Cryptosporidium', 'Cryptosporidium caused disease or disorder', 'Cryptosporidium infection', 'Cryptosporidioses', 'intestinal cryptosporidiosis', 'Cryptosporidial gastroenteritis']",1733,,1549,C0520796,,C128408,,D003457,007.4,A07.2,10011502,
mondo:0015476,cysts and fistulae of the face and oral cavity,,,,155835,,,,,,,,,
mondo:0015477,pinnae fistula or cyst,,,,155838,,,,,,,,,
mondo:0015478,paramedian facial cleft,['Tessier number 1-1 and 2-12 facial cleft'],,,155867,,,,,,,,,
mondo:0015479,submucosal cleft palate,,,,155878,,,,,,,,,
mondo:0015480,coloboma of superior eyelid,['superior palpebral coloboma'],,,155884,,,,,,,,,
mondo:0015481,coloboma of inferior eyelid,['Inferior palpebral coloboma'],,,155889,,,,,,,,,
mondo:0015482,otomandibular dysplasia,,,,155896,,,,,,,,,
mondo:0015483,mandibulofacial dysostosis,['bilateral and symmetric oto-mandibular dysplasia'],,,155899,,"['0.0978', '0.4165', '0.3796', '-0.09174', '0.2233', '-0.2566', '-0.07367', '0.1661', '-0.1804', '-0.2189', '0.2583', '-0.1727', '-0.508', '-0.03247', '-0.00505', '0.151', '0.1558', '-0.1743', '0.2041', '-0.271', '-0.2673', '-0.06805', '0.3328', '0.2727', '0.2974', '0.2786', '-0.1451', '-0.06946', '0.27', '-0.3208', '0.0873', '-0.1813', '-0.0917', '0.1987', '-0.2042', '-0.2325', '0.0007243', '-0.08215', '-0.2026', '-0.6055', '0.1234', '-0.3784', '0.25', '-0.3684', '0.02005', '-0.229', '-0.05014', '0.1937', '-0.1842', '-0.2852', '0.1953', '-0.265', '-0.436', '-0.2147', '-0.1229', '-0.65', '0.4011', '-0.02382', '-0.4866', '-0.1437', '-0.1898', '0.1763', '0.2429', '0.4482', '0.00473', '0.10394', '0.11053', '0.2144', '-0.295', '0.2053', '-0.314', '0.428', '0.4795', '-0.073', '0.1927', '0.599', '0.0692', '-0.05185', '-0.4521', '-0.4226', '0.2317', '0.4014', '0.3962', '0.73', '0.582', '0.0256', '-0.226', '0.3542', '-0.1661', '0.123', '-0.1238', '0.615', '0.2472', '0.185', '1.039', '-0.2356', '0.4165', '-0.617', '0.0688', '-0.1355']",,,D008342,,,10051456,
mondo:0015484,cysticercosis,"['pork tapeworm infection', 'tapeworm infection: intestinal taenia solum', 'neurocysticercosis', 'tenia solium infectious disease', 'tapeworm infection: pork', 'intestinal taenia solium infection', 'tapeworm infection: [intestinal taenia solium] or [pork]']",10079,,1560,C0338437,,C34520,0007231,D003551,123.1,B69,10011775,
mondo:0015485,primary hereditary glaucoma,['primary glaucoma'],,,156005,,,,,,,,,
mondo:0015486,keratoconus,"['conical cornea', 'isolated keratoconus', 'keratoconus (disease)', 'keratoconus', 'noninflammatory corneal thining', 'KC']",10126,,2335,C0022578,"['-0.2142', '-0.11273', '-0.1284', '0.2844', '-0.4622', '-0.02478', '0.1383', '0.4214', '-0.6294', '-0.2455', '0.28', '0.096', '-0.613', '0.453', '-0.5063', '-0.1478', '-0.02168', '0.1719', '-0.00207', '-0.6074', '0.1322', '0.5903', '-0.5366', '-0.1512', '-0.1903', '0.10565', '0.1787', '0.2695', '0.1967', '0.5747', '0.2876', '0.0964', '0.0503', '0.3638', '0.499', '0.515', '-0.3975', '-0.3064', '0.10944', '-0.2825', '0.8335', '0.1707', '-0.4658', '-0.2279', '-0.648', '-0.1674', '-0.1497', '-0.2235', '0.941', '0.554', '-0.0962', '-0.2917', '0.537', '-1.054', '0.4272', '-0.2438', '-0.111', '0.011246', '-0.5137', '-0.6685', '-0.3562', '-0.2472', '-0.08014', '0.309', '-0.0773', '-0.04343', '0.441', '0.78', '-0.2319', '1.163', '-0.9077', '0.1836', '-0.2495', '-0.0767', '-0.2576', '-0.1307', '0.0928', '0.519', '0.1231', '-0.0801', '-0.2068', '-0.287', '-0.7183', '0.977', '-0.1627', '-0.474', '0.2551', '0.04172', '0.4155', '0.5225', '-0.3367', '-0.03656', '-0.1138', '0.488', '0.669', '-0.02226', '0.2227', '-0.3616', '-0.2954', '0.0413']",C26806,,D007640,371.60,,10023353,0000563
mondo:0015487,fatal infantile encephalocardiomyopathy,"['fatal infantile COX deficiency', 'fatal infantile encephalomyopathy', 'cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency', 'fatal infantile cytochrome C oxidase deficiency', 'fatal infantile cardioencephalomyopathy due to cytochrome c oxidase deficiency', 'fatal infantile cardioencephalomyopathy due to cytochrome C oxidase deficiency']",0050713,,1561,,"['0.1024', '-0.614', '-0.2184', '0.7505', '-0.01513', '-0.511', '0.6577', '0.5093', '-0.4812', '-0.3062', '0.4773', '-0.2366', '-0.3994', '0.4382', '-0.6953', '0.2301', '-1.036', '-0.102', '-0.606', '-0.8643', '0.00275', '0.1277', '0.6123', '-0.1897', '0.3076', '-0.2281', '0.0362', '0.4224', '-0.05002', '-0.4736', '0.8105', '-0.2954', '0.637', '0.511', '0.05313', '-0.6743', '-0.1131', '-0.3477', '0.917', '-0.5073', '-0.0734', '0.258', '-0.0641', '0.743', '0.2307', '0.2927', '0.3218', '0.8', '0.579', '-0.2595', '-0.3813', '0.0439', '0.53', '0.2634', '0.4348', '-0.619', '-0.432', '0.3035', '-0.4807', '0.005455', '-0.2756', '0.4534', '0.4033', '-0.9556', '-0.8853', '0.1396', '0.1307', '0.464', '-0.98', '-0.1219', '-0.3083', '0.2393', '0.02437', '-0.1019', '0.1681', '0.682', '-0.2374', '-0.0314', '-0.1967', '0.4617', '0.04892', '-0.318', '-0.3215', '-0.6304', '1.305', '-0.1543', '0.757', '-0.06015', '0.5356', '0.347', '0.4292', '-0.0743', '-0.1788', '0.2573', '0.962', '0.9517', '0.134', '-0.6187', '-0.3289', '-0.3896']",,,,,,,
mondo:0015488,predominantly large-vessel vasculitis,,,,156140,,,,,,,,,
mondo:0015489,predominantly medium-vessel vasculitis,,,,156143,,,,,,,,,
mondo:0015490,predominantly small-vessel vasculitis,,,,156146,,,,,,,,,
mondo:0015491,immune complex mediated vasculitis,,,,156149,,,,,,,,,
mondo:0015492,anti-neutrophil cytoplasmic antibody-associated vasculitis,"['AAV', 'antineutrophil cytoplasmic antibody-associated vasculitis', 'ANCA-associated vasculitis']",,,156152,C2717865,,,,D056648,,,,
mondo:0015493,"lipoatrophy with diabetes, leukomelanodermic papules, liver steatosis, and hypertrophic cardiomyopathy",,,,156156,,,,,,,,,
mondo:0015494,isolated dystonia,"['nonsyndromic dystonic disorder', 'Pure dystonia', 'nonsyndromic dystonia (disease)']",,,156159,,"['0.5283', '0.336', '-0.00652', '-0.39', '-0.0274', '-0.9673', '0.587', '-0.082', '-0.75', '-0.01593', '0.9126', '0.581', '-0.43', '0.5293', '0.5747', '0.4614', '-0.2773', '-0.607', '-0.569', '-1.131', '-0.3657', '-0.06238', '0.014114', '-0.0792', '-0.309', '-0.02469', '0.03793', '0.1458', '0.0407', '0.1981', '0.3262', '0.1716', '1.106', '-0.1274', '0.6216', '-0.03122', '0.53', '0.1086', '0.3909', '-0.641', '0.5527', '-0.084', '-0.4146', '0.2644', '0.5654', '-0.0778', '-0.2356', '0.317', '0.517', '0.5547', '0.1791', '0.2502', '0.5254', '0.1643', '0.1904', '-0.06287', '0.1655', '0.78', '0.1809', '-0.268', '-0.817', '-0.3967', '-0.01773', '-0.566', '-1.055', '0.609', '0.3923', '0.281', '-0.406', '0.5317', '-0.1718', '-0.0808', '0.1183', '-0.3774', '0.3713', '0.486', '0.6694', '0.1788', '-0.02296', '-0.2925', '-0.1763', '0.1809', '0.192', '0.3826', '0.8535', '-0.1796', '0.0722', '0.2737', '1.545', '0.1693', '0.1678', '0.1931', '0.4097', '0.4766', '0.8657', '-0.064', '-0.749', '0.1193', '0.128', '-0.2302']",,,,,,,
mondo:0015496,macroglossia,"['giant tongue', 'enlarged tongue']",,,156207,C0024421,,,,D008260,,,10025391,
mondo:0015497,hypoglossia/aglossia,,,,156212,,,,,,,,,
mondo:0015498,oromandibular-limb anomalies syndrome,,,,156215,CN199634,,,,,,,,
mondo:0015499,paralytic facial malformation,,,,156224,,,,,,,,,
mondo:0015500,facial arteriovenous malformation,,,,156230,,,,,,,,,
mondo:0015503,nose and cavum anomaly,,,,156246,,,,,,,,,
mondo:0015504,larynx anomaly,,,,156249,,,,,,,,,
mondo:0015505,tracheal anomaly,,,,156252,,,,,,,,,
mondo:0015508,hereditary parenchymatous liver disease,['genetic parenchymatous liver disease'],,,156604,CN199641,,,,,,,,
mondo:0015509,hereditary biliary tract disease,['genetic biliary tract disease'],,,156607,CN199642,,,,,,,,
mondo:0015514,hereditary endocrine growth disease,"['growth disorder', 'genetic endocrine growth disease']",,,156643,CN237424,,,,D006130,,,,
mondo:0015515,carnitine palmitoyltransferase II deficiency,"['Carnitine palmitoyltransferase II (CPT II) deficiency', 'CPT II deficiency', 'Carnitine palmitoyltransferase 2 deficiency', 'lethal neonatal carnitine palmitoyltransferase II deficiency', 'infantile carnitine palmitoyltransferase II deficiency', 'Carnitine palmitoyltransferase deficiency type 2', 'late-onset carnitine palmitoyltransferase II deficiency', 'CPTII', 'CPT2', 'CPT-II']",0060235,,157,C0342790,"['0.2644', '-0.1536', '0.2498', '0.05786', '0.2046', '-0.3782', '-0.13', '0.3125', '0.087', '0.5664', '-0.1451', '-0.1855', '0.2583', '0.0965', '-0.6875', '0.1537', '-0.2568', '0.3262', '-0.2573', '-0.699', '0.39', '-0.299', '0.636', '-0.2852', '-0.698', '-0.2106', '-0.4517', '-0.663', '0.2216', '-0.663', '0.3076', '0.4153', '0.622', '-0.2156', '-0.4165', '-0.549', '-1.08', '-0.28', '-0.183', '0.03296', '0.07135', '-1.12', '0.744', '0.09174', '0.4253', '-0.432', '-0.1622', '0.8276', '-0.04358', '0.6416', '-0.4539', '-0.1433', '-0.0184', '0.00883', '-0.2008', '-1.072', '0.1064', '0.079', '-0.1532', '-0.1736', '-0.0759', '0.07654', '0.6577', '0.39', '0.014656', '0.1339', '0.1552', '0.1414', '-0.6484', '-0.1609', '0.3467', '0.1002', '0.4368', '0.4702', '0.59', '1.142', '0.4404', '0.1311', '0.07855', '0.4375', '0.3472', '0.148', '-0.1211', '-0.1796', '0.8887', '0.6357', '0.4695', '0.769', '0.4238', '-0.2344', '0.0389', '0.3367', '0.407', '0.1821', '0.7007', '0.9165', '0.2927', '-0.4272', '-0.188', '-0.668']",C114766,,C535589,277.85,,,
mondo:0015516,symbrachydactyly of hands and feet,['De Smet-Fabry-Fryns syndrome'],,,1570,,,,,,,,,
mondo:0015517,common variable immunodeficiency,"['sporadic hypogammaglobulinemia', 'acquired hypogammaglobulinemia', 'common variable agammaglobulinemia', 'primary antibody deficiency', 'hypogamma-globulinemia, acquired', 'CVID', 'primary hypogammaglobulinemia', 'acquired agammaglobulinemia', 'secondary hypogammaglobulinemia', 'common variable immune deficiency', 'Immunoglobulin deficiency, late-onset', 'common variable hypogamma-globulinemia', 'idiopathic immunoglobulin deficiency']",12177,,1572,C0009447,"['1.034', '0.4302', '-0.5063', '-0.3433', '0.2347', '-0.438', '0.7676', '0.4263', '-0.3972', '-0.4375', '-0.1421', '0.2136', '-0.3381', '0.1903', '0.4548', '-0.1711', '-0.506', '-0.504', '-0.3591', '-0.2465', '-0.3533', '-0.03983', '0.9053', '-0.631', '0.05228', '0.00758', '-0.2289', '0.1357', '-0.1948', '-0.1738', '0.4106', '0.325', '0.4487', '0.1881', '0.489', '-0.1765', '-0.5063', '0.2296', '-0.506', '0.1731', '-0.355', '0.447', '0.4963', '-0.4224', '0.057', '-0.2095', '-0.2262', '-0.3936', '0.2351', '0.3416', '0.1926', '-0.3135', '0.1584', '0.446', '-0.004673', '0.519', '-0.3118', '-0.5723', '-0.2305', '0.3625', '0.2186', '0.906', '0.3281', '0.2673', '0.4277', '0.3809', '0.2454', '0.6655', '-0.2632', '0.779', '0.05408', '-0.917', '-0.0872', '-0.12317', '0.775', '-0.0167', '0.5254', '0.1736', '0.3562', '-0.2266', '0.2905', '-0.319', '0.0859', '-0.0045', '-0.344', '0.5083', '0.6235', '0.1688', '0.4998', '-0.577', '0.466', '0.03293', '-0.3867', '-0.04318', '0.816', '0.5356', '0.4924', '0.04776', '-0.336', '-0.3142']",C26725,,D017074,279.06,,10021449,
mondo:0015518,infantile bilateral striatal necrosis,"['striatonigral degeneration infantile', 'striatal degeneration familial', 'IBSN', 'infantile striatonigral degeneration', 'SNDI', 'infantile bilateral striatal necrosis', 'infantile striatonigral necrosis']",,,1576,C0795996,"['-0.1602', '0.264', '0.1573', '-0.0696', '-0.07513', '-1.408', '0.536', '0.2642', '-0.765', '-0.2722', '-0.0079', '-0.3135', '-0.529', '-0.3357', '0.4336', '-0.2092', '-0.669', '-0.2927', '0.05475', '-1.196', '-0.01564', '0.05368', '0.339', '-0.8374', '0.2328', '0.1405', '-0.09204', '-0.2406', '-1.154', '0.381', '0.1553', '0.726', '0.1752', '0.143', '-0.05078', '0.603', '-0.4849', '-0.53', '-0.9004', '-0.2852', '0.1948', '-0.2668', '0.3364', '-0.4475', '0.6074', '-0.316', '-0.4868', '-0.3152', '-0.7017', '0.0853', '-0.0351', '0.6655', '0.0541', '0.0843', '0.488', '-0.2257', '0.57', '-0.1978', '-1.012', '0.5444', '-0.2064', '-0.10974', '0.6714', '0.2017', '-0.4456', '-0.166', '0.9736', '-0.02528', '-0.518', '0.8013', '-0.1838', '0.1683', '-0.1671', '-0.1864', '0.9043', '0.399', '0.231', '0.05075', '0.0966', '-0.1558', '-0.3132', '0.0606', '-0.3257', '0.7275', '0.7817', '0.2915', '-0.0572', '0.6416', '-0.0942', '0.2035', '1.027', '0.09875', '0.01399', '0.01878', '0.01958', '0.01364', '0.749', '-0.1255', '0.03714', '-0.4126']",,,,,G23.2,,
mondo:0015519,congenital or early infantile CACH syndrome,,,,157713,,"['-0.05157', '0.1057', '0.04846', '-0.01851', '0.0662', '-0.176', '0.005844', '0.1238', '-0.1337', '-0.06165', '-0.0793', '-0.004704', '-0.01004', '0.01182', '-0.03836', '-0.0617', '-0.05283', '-0.09503', '-0.04575', '-0.2224', '0.003572', '-0.08185', '0.06506', '-0.08673', '0.0438', '-0.04218', '-0.05176', '-0.04684', '0.04037', '-0.10864', '0.1142', '0.014984', '0.1592', '0.11145', '0.014786', '-0.01767', '-0.02185', '-0.05234', '-0.02388', '-0.09454', '0.05075', '-0.1276', '0.03595', '-0.03607', '-0.03078', '-0.05728', '-0.0754', '0.099', '0.013084', '0.0822', '-0.01591', '0.007496', '0.02397', '-0.02557', '-0.02216', '-0.10504', '0.122', '-0.03114', '-0.1846', '0.01237', '0.0836', '0.0539', '0.02019', '-0.0001664', '0.01674', '-0.01286', '0.2205', '0.1194', '-0.11487', '0.11035', '-0.1219', '0.03897', '0.0676', '-0.0982', '0.05527', '0.01955', '0.02548', '-0.0389', '-0.0801', '-0.02284', '0.01553', '-0.0004096', '-0.1096', '0.1556', '0.03403', '-0.004036', '0.06226', '0.0989', '0.1405', '0.0412', '0.09125', '0.1346', '0.01729', '0.06586', '0.1956', '0.05588', '0.2092', '-0.2054', '0.01454', '0.0341']",,,,,,,
mondo:0015520,late infantile CACH syndrome,,,,157716,CN199659,"['-0.0352', '0.1117', '0.03093', '0.02487', '0.03067', '-0.1099', '-0.01326', '0.1054', '-0.12036', '-0.03146', '-0.0673', '0.01765', '-0.01307', '0.00901', '0.007572', '-0.0682', '-0.08215', '-0.09375', '-0.004894', '-0.1512', '-0.01588', '-0.04492', '0.05054', '-0.06015', '0.03207', '-0.02548', '-0.05252', '-0.03622', '-0.0343', '-0.04315', '0.0964', '-0.001425', '0.11774', '0.0673', '0.04184', '0.006344', '-0.0398', '-0.04892', '-0.0409', '-0.0798', '0.02019', '-0.1112', '0.0601', '-0.01779', '-0.00773', '-0.0625', '-0.08655', '0.0994', '-0.03027', '0.0856', '0.02155', '0.04495', '-0.04807', '0.001158', '-0.0008407', '-0.1017', '0.11755', '-0.0686', '-0.1255', '0.02298', '0.07043', '0.0423', '0.03032', '0.02396', '0.06058', '-0.01258', '0.1646', '0.0817', '-0.0731', '0.1091', '-0.0791', '0.01357', '0.0747', '-0.0824', '0.0624', '0.04767', '0.00801', '0.02074', '-0.08167', '-0.05753', '0.02034', '0.01991', '-0.08734', '0.1383', '0.02899', '-0.01027', '0.04037', '0.10126', '0.1511', '0.05383', '0.05276', '0.11865', '-0.007553', '0.03287', '0.1554', '0.03534', '0.162', '-0.1705', '-0.003166', '0.02673']",,,,,,,
mondo:0015521,juvenile or adult CACH syndrome,,,,157719,CN199660,"['-0.0307', '0.1322', '0.01467', '0.00807', '0.03955', '-0.169', '0.00598', '0.1287', '-0.079', '-0.03473', '-0.0531', '0.006573', '-0.03296', '0.02611', '-0.00805', '-0.08575', '-0.0381', '-0.06555', '-0.05276', '-0.1946', '-0.04315', '-0.0708', '0.04913', '-0.0894', '0.03955', '0.00623', '-0.05698', '-0.064', '0.0421', '-0.06244', '0.1047', '-0.00707', '0.1433', '0.0665', '0.0907', '-0.03693', '-0.03568', '-0.0689', '-0.0339', '-0.0796', '0.05933', '-0.1375', '0.03494', '-0.0731', '0.02524', '-0.06174', '-0.1001', '0.07056', '0.02586', '0.0439', '0.01333', '0.02486', '-0.02344', '-0.0032', '-0.05194', '-0.09235', '0.1014', '-0.07446', '-0.1603', '0.01752', '0.0894', '0.0445', '0.02383', '-0.0146', '0.0349', '0.0411', '0.2042', '0.05627', '-0.05975', '0.10583', '-0.083', '-0.01553', '0.07745', '-0.09216', '0.0591', '0.03574', '-0.0002335', '0.03494', '-0.0941', '-0.05627', '0.04797', '-0.02132', '-0.0788', '0.133', '0.02141', '-0.02089', '0.03558', '0.0815', '0.104', '0.02527', '0.0713', '0.1318', '0.002083', '0.03568', '0.2058', '0.02809', '0.1614', '-0.1453', '-0.0425', '0.0554']",,,,,,,
mondo:0015523,epithelioid hemangioendothelioma,"['epithelioid angiosarcoma', 'epithelioid hemangioendothelioma', 'malignant epithelioid hemangioendothelioma', 'epithelioid angioendothelioma']",0080190,,157791,C0206732,,C3800,,D018323,,,,
mondo:0015524,hyperplastic polyposis syndrome,['serrated polyposis'],,175020,157798,CN199665,,C165469,,,,,,
mondo:0015525,congenital pseudoarthrosis of the limbs,"['congenital pseudoarthrosis', 'congenital pseudarthrosis of the limbs']",,,157808,,,,,C535762,,,,
mondo:0015526,cold-induced sweating syndrome,"['Sohar-Crisponi syndrome', 'CISS']",0060294,,157820,CN043579,"['-0.04352', '0.2559', '-0.1865', '-0.352', '-0.05463', '-0.7783', '-0.06647', '0.513', '-0.1156', '-0.5317', '0.1826', '0.161', '-0.071', '-0.244', '-0.2524', '1.248', '0.3323', '-0.3115', '-0.2157', '-0.3142', '0.02437', '0.16', '0.1549', '-0.3433', '-0.1465', '-0.425', '0.1599', '-0.205', '0.1482', '-0.389', '0.5317', '0.06213', '-0.11554', '0.1868', '-0.10223', '-0.1742', '0.00877', '-0.2021', '-0.2137', '-0.0843', '-0.6084', '-0.353', '-0.11285', '-0.3252', '0.5034', '-0.0697', '0.03967', '0.5815', '-0.2249', '0.243', '-0.3982', '0.1659', '-0.116', '0.4624', '0.295', '-0.4744', '0.3994', '0.3157', '0.2646', '0.0352', '0.1323', '0.08185', '-0.1195', '0.6465', '-0.1748', '-0.2595', '0.612', '0.6753', '-0.4417', '0.2446', '-0.5923', '0.3933', '0.2598', '0.4287', '0.277', '0.655', '0.2003', '0.1787', '0.2076', '0.2725', '0.32', '-0.05054', '0.573', '0.511', '0.1086', '0.1091', '0.2041', '0.574', '0.1881', '0.02661', '0.2148', '0.068', '0.5747', '0.509', '0.865', '0.1907', '0.1393', '-0.4482', '-0.02744', '0.1368']",,,,,,,
mondo:0015528,congenital epulis,"['congenital gingival cell tumor', 'congenital Epulides', 'congenital gingival cell tumour', 'gingival granular cell tumor', 'Neumann tumour', 'Neumann tumor', 'congenital epulis', 'congenital granular cell tumour', 'gingival granular cell tumour', 'congenital granular cell tumor']",7280,,157826,C0376319,,C4675,,D005887,,,,
mondo:0015529,paroxysmal Hemicrania,,,,157835,C1399352,,,1001822,D051302,339.03,,10019461,
mondo:0015530,trigeminal autonomic cephalalgia,,,,157843,C1565172,,C117074,,D051303,339.09,,,
mondo:0015531,non-Langerhans cell histiocytosis,"['histiocytosis, non-Langerhans-cell', 'non-Langerhans-cell histiocytosis']",4330,,157987,C0019624,,,,D015616,288.4,,,
mondo:0015532,generalized eruptive histiocytosis,"['generalized eruptive histiocytoma', 'generalised eruptive histiocytoma']",,,157991,C0347404,,,,,,,,
mondo:0015533,benign cephalic histiocytosis,,,,157997,C0347403,,,,,216.8,,,
mondo:0015534,juvenile xanthogranuloma,"['JXG', 'juvenile xanthogranuloma', 'Naevoxanthoendothelioma', 'xanthoma neviforme', 'multiple eruptive juvenile xanthogranuloma']",4424,,158000,C0043324,,C3451,1000311,D014972,,,,
mondo:0015535,xanthoma disseminatum,['Montgomery syndrome'],,,158003,C0043322,,,,,,,10052575,
mondo:0015536,papular xanthoma,,,,158008,CN199692,,,,,,,,
mondo:0015537,necrobiotic xanthogranuloma,['NXG'],,,158011,C1275339,,,1001376,D058252,709.8,,,
mondo:0015538,indeterminate dendritic cell tumor,"['indeterminate Dendritic cell tumour', 'IDCT', 'indeterminate dendritic cell tumor', 'indeterminate Dendritic cell tumor', 'indeterminate cell histiocytosis']",,,158019,C2825741,,C81767,,,,,,
mondo:0015539,progressive nodular histiocytosis,,,,158022,,,,,,,,,
mondo:0015540,hemophagocytic syndrome,"['familial histiocytic reticulosis', 'hemophagocytic lymphohistiocytosis', 'hemophagocytic disorder', 'haemophagocytic syndrome', 'HLH', 'FHL', 'familial erythrophagocytic lymphohistiocytosis', 'familial hemophagocytic lymphohistiocytosis', 'hemophagocytic syndrome']",0050120,,158032,C3887558,,C35439,,,288.8,,10058125,
mondo:0015541,hereditary hemophagocytic lymphohistiocytosis,"['genetic hemophagocytic syndrome', 'primary hemophagocytic lymphohistiocytosis', 'familial hemophagocytic lymphohistiocytosis', 'genetic hemophagocytic lymphohistiocytosis']",,,540,,,,,,238.79,,10070904,
mondo:0015542,secondary hemophagocytic lymphohistiocytosis,"['reactive hemophagocytic syndrome', 'acquired hemophagocytic syndrome', 'acquired hemophagocytic lymphohistiocytosis']",,,158041,CN199700,,C121184,,,,,,
mondo:0015544,acquired hemophagocytic lymphohistiocytosis associated with malignant disease,,,,158057,CN199702,,,,,,,,
mondo:0015545,macrophage activation syndrome,"['MAS', 'reactive hemophagocytic lymphohistiocytosis']",,,158061,C1096155,,C114471,1001806,D055501,,,10053867,
mondo:0015546,non-distal monosomy 10q,"['non-distal deletion 10q', 'non-distal monosomy type 10q', 'non-telomeric monosomy 10q']",,,1581,,,,,,,,,
mondo:0015547,hereditary dementia,['genetic dementia'],,,158124,,,,,,,,,
mondo:0015548,Huntington disease-like syndrome,['Huntington disease phenocopy syndrome'],,,158266,C3711380,,,,C580174,333.99,,,
mondo:0015550,suprabasal epidermolysis bullosa simplex,"['epidermis suprabasal layer epidermolysis bullosa simplex', 'epidermolysis bullosa simplex of epidermis suprabasal layer']",,,158661,C4511300,,,,,,,,
mondo:0015552,acral dystrophic epidermolysis bullosa,"['DEB-ac', 'DEB, acral']",,,158673,CN199731,,,,,,,,
mondo:0015553,"dystrophic epidermolysis bullosa, nails only","['nails-only DDEB', 'dominant dystrophic epidermolysis bullosa, nails only', 'nails-only DEB', 'DEB-na']",,,158676,CN199732,,,,,,,,
mondo:0015554,typical urticaria pigmentosa,,,,158766,,,,,,,,,
mondo:0015555,plaque-form urticaria pigmentosa,,,,158769,,,,,,,,,
mondo:0015556,nodular urticaria pigmentosa,,,,158772,,,,,,,,,
mondo:0015557,Smouldering systemic mastocytosis,,,,158775,,,,,,,,,
mondo:0015558,isolated bone marrow mastocytosis,,,,158778,,,,,,,,,
mondo:0015559,lymphoadenopathic mastocytosis with eosinophilia,,,,158793,,,,,,,,,
mondo:0015562,distal monosomy 17q,"['monosomy 17q', 'distal 17q deletion', 'telomeric deletion 17q', '17q monosomy', 'distal monosomy type 17q', 'partial monosomy 17q', 'monosomy 17qter', '17q deletion', 'deletion 17q', 'chromosome 17q deletion']",,,1597,C4275171,,,,,,,,
mondo:0015564,Castleman disease,"['lymphoid hamartoma', 'angiofollicular lymph hyperplasia', 'ALNH', 'Castleman disease', 'Castleman^s tumour', 'angiofollicular lymphoid hyperplasia', 'Castleman^s disease', 'Castleman^s tumor', 'AFLH', 'giant lymph node hyperplasia', 'angiofollicular ganglionic hyperplasia', 'GLNH', 'angiofollicular lymph node hyperplasia']",0111157,,160,CN199886,,C3056,1001332,D005871,,D47.Z2,10050251,
mondo:0015565,cap polyposis,"['Cap inflammatory polyposis', 'eroded polypoid hyperplasia', 'inflammatory myoglandular polyps', 'polypoid prolapsing folds']",,,160148,C4303971,,,,,,,,
mondo:0015566,2q24 microdeletion syndrome,"['deletion 2q24', 'Del(2)(q24)', '2q24 deletion', 'chromosome 2q24 microdeletion syndrome', 'monosomy 2q24']",,,1617,CN036809,,,,C538316,,,,
mondo:0015567,cataract-glaucoma syndrome,['cataract - glaucoma'],,,162,CN199931,,,,,,,,
mondo:0015568,isolated congenital nasal pyriform aperture stenosis,"['isolated nasal pyriform aperture hypoplasia', 'isolated apertura pyriformis stenosis']",,,162516,,,,,,,,,
mondo:0015569,congenital nasal pyriform aperture stenosis with holoprosencephaly,['apertura pyriformis with holoprosencephaly'],,,162521,,,,,,,,,
mondo:0015570,isolated congenital auditory ossicle malformation,['congenital auditory ossicle malformation without external ear abnormality'],,,162526,,,,,,,,,
mondo:0015571,deletion 5q35,"['telomeric deletion 5q', 'distal 5q deletion', 'deletion type 5q35', 'Del (5)(qter)', 'Del (5)(q35)', 'monosomy 5q35']",,,1627,,,,,C537647,,,,
mondo:0015573,subacute cutaneous lupus erythematosus,,,,163525,C0024140,,C117111,,,,L93.1,10057903,
mondo:0015574,chronic cutaneous lupus erythematosus,"['cutaneous lupus erythematosus, chronic']",,,163531,CN226705,,,,,,,10057929,
mondo:0015579,Hb Bart^s hydrops fetalis,"['Hemoglobin Bart^s hydrops fetalis', 'Alpha-thalassemia major', 'Alpha-thalassemia hydrops fetalis', 'homozygous alpha0-thalassemia', 'Haemoglobin Bart^s hydrops fetalis']",,,163596,,,,,,282.49,,,
mondo:0015580,distal monosomy 7q36,"['distal deletion 7q36', 'monosomy 7qter', 'distal monosomy type 7q36', 'telomeric deletion 7q36']",,,1636,,,,,,,,,
mondo:0015583,2p21 microdeletion syndrome,"['monosomy 2p21', '2p21 deletion syndrome', 'Del(2)(p21)', '2p21 microdeletion syndrome']",,,163693,CN199952,"['0.1267', '0.8486', '0.3293', '-0.157', '0.06995', '-0.4219', '-0.257', '1.243', '-0.5337', '0.3342', '-0.0572', '-0.1394', '0.525', '-0.5806', '-0.0948', '0.6357', '0.256', '-0.212', '-0.396', '-0.455', '0.02676', '-0.3647', '0.9287', '-0.02718', '0.5693', '-0.2517', '-0.3433', '0.4583', '0.0683', '-0.2766', '0.3806', '-0.1334', '0.5215', '-0.1422', '-0.225', '-0.3013', '-0.175', '-0.4424', '-0.271', '-0.611', '-0.3406', '-0.02303', '0.1682', '-0.2688', '-0.237', '-0.233', '0.3784', '0.493', '-0.2407', '-0.4658', '-0.4192', '-0.3884', '-0.1561', '0.08154', '0.0924', '-0.7236', '0.654', '0.4397', '-0.0277', '0.7817', '-0.228', '0.0373', '0.194', '0.4695', '-0.1509', '-0.2314', '0.3174', '0.304', '-0.417', '0.0965', '-0.147', '0.535', '0.2294', '0.10547', '-0.01376', '0.2302', '0.4487', '-0.4707', '-0.3564', '0.74', '0.6167', '0.2078', '-0.4214', '0.1832', '0.1053', '0.09344', '-0.0935', '0.303', '0.395', '-0.1087', '-0.3494', '0.5234', '-0.07074', '-0.04968', '1.079', '0.488', '-0.3315', '-0.3376', '0.2842', '-0.2888']",,,,,,,
mondo:0015584,febrile infection-related epilepsy syndrome,"['AERRPS', 'fever-induced refractory epileptic encephalopathy in school-aged children', 'devastating epileptic encephalopathy in school-aged children', 'FIRES', 'DESC syndrome', 'acute encephalitis with refractory repetitive partial seizures', 'acute non-herpetic encephalitis with severe refractory status epilepticus', 'status epilepticus owing to presumed encephalitis', 'severe refractory status epilepticus owing to presumed encephalitis', 'idiopathic catastrophic epileptic encephalopathy']",,,163703,CN199955,,,,,,,,
mondo:0015585,cryptogenic late-onset epileptic spasms,['late-onset infantile spasms'],,,163708,,,,,,,,,
mondo:0015586,benign familial mesial temporal lobe epilepsy,['benign FMTLE'],,,163717,CN226709,,,,,,,,
mondo:0015587,rolandic epilepsy-speech dyspraxia syndrome,,,,163721,CN199957,"['1.16', '0.1299', '-0.3113', '-0.17', '-0.439', '-0.4797', '0.8633', '0.397', '-0.6836', '-0.3662', '0.1078', '-0.2247', '-0.3713', '0.4814', '-0.0436', '-0.04926', '-0.297', '-0.455', '-0.542', '-0.5557', '-0.2334', '0.666', '0.09143', '-0.4033', '-0.357', '-0.0659', '0.02647', '-0.10913', '-0.6235', '0.4436', '0.3184', '-0.668', '0.2612', '0.297', '0.7734', '0.43', '-0.1567', '-0.06854', '-0.0913', '-0.6123', '-0.1981', '-0.3123', '0.1602', '-0.341', '-0.462', '-0.733', '-0.3364', '0.2786', '0.692', '0.5947', '-0.07025', '0.1603', '-0.0351', '-0.5312', '0.1835', '-0.17', '-0.3225', '0.01497', '-0.1169', '0.3257', '-0.838', '0.4878', '0.831', '-0.2886', '-0.3203', '1.487', '0.0206', '-0.06015', '-1.026', '0.7603', '1.064', '1.06', '-0.01634', '-0.539', '0.2732', '0.682', '0.9565', '0.4673', '-0.4707', '0.3', '-0.2421', '0.8164', '0.4106', '0.3767', '0.4277', '0.1406', '0.1422', '0.789', '0.89', '0.3586', '0.1126', '0.07776', '-0.3752', '0.2505', '0.273', '0.349', '0.1802', '-0.5337', '0.2489', '0.2109']",,,,,,,
mondo:0015588,limbic encephalitis,,0080741,,163892,,,,,D020363,323.9,,,
mondo:0015589,paraneoplastic limbic encephalitis,['limbic encephalitis'],,,163895,,,C4350,,,323.81,,,
mondo:0015590,classic paraneoplastic limbic encephalitis,"['classic paraneoplastic limbic encephalitis, with or without intracellular antigens']",,,163898,,,,,,,,,
mondo:0015591,limbic encephalitis associated with antibodies to cell membrane antigens,,,,163903,,,,,,,,,
mondo:0015592,limbic encephalitis with LGI1 antibodies,['limbic encephalitis with leucine-rich glioma-inactivated 1 antibodies'],,,163908,,,,,,,,,
mondo:0015593,limbic encephalitis with nCMAgs antibodies,['limbic encephalitis with novel cell membrane antigen antibodies'],,,163914,,,,,,,,,
mondo:0015595,posttransplant acute limbic encephalitis,['pale'],,,163921,,,,,,,,,
mondo:0015596,non-herpetic acute limbic encephalitis,,,,163924,,,,,,,,,
mondo:0015597,pustulosis palmaris et plantaris,"['PPP', 'palmoplantar pustulosis', 'acropustulosis', 'localised pustular psoriasis', 'LPP', 'pustulosis of palm and sole', 'localized pustular psoriasis', 'pustular psoriasis of the palms and/or soles']",4398,,163927,,,C34888,,D011565,696.1,L40.3,10050185,
mondo:0015599,atopic keratoconjunctivitis,,,,163934,C1274788,,,,,370.49,H16.2,10069664,
mondo:0015600,"X-linked intellectual disability, Cilliers type",['X-linked intellectual disability-microcephaly-testicular failure syndrome'],,,163971,CN226710,,,,,,,,
mondo:0015601,"X-linked intellectual disability, van Esch type","['VEODS', 'Van Esch-O^Driscoll syndrome', 'mental retardation, X-Linked, syndromic, Van Esch-O^Driscoll type', 'Van Esch-O^Driscoll syndrome, X-linked recessive']",0111840,301030,163976,CN226711,"['-0.401', '0.292', '0.311', '-0.4395', '0.2319', '-0.53', '-0.0652', '0.6763', '-0.2996', '-0.32', '0.2761', '0.1595', '0.10114', '-0.2876', '0.0298', '0.10175', '0.476', '0.1123', '-0.4185', '-0.709', '0.06244', '0.163', '0.2515', '-0.131', '0.1881', '-0.194', '-0.02061', '-0.1886', '0.4207', '-0.3633', '0.5063', '-0.10016', '0.3157', '0.3962', '-0.1964', '-0.4575', '-0.4783', '-0.353', '-0.33', '-0.4612', '0.02527', '0.086', '-0.005726', '-0.2416', '-0.2317', '-0.5415', '0.312', '0.1195', '-0.0654', '-0.4338', '-0.11786', '-0.3984', '-0.3704', '-0.2013', '0.2488', '-0.2065', '0.1697', '-0.2615', '0.2203', '0.2183', '-0.0616', '0.10724', '0.08264', '0.00247', '-0.0778', '0.2303', '-0.0949', '0.571', '-0.6826', '0.329', '-0.7046', '0.4517', '0.2988', '-0.389', '-0.05124', '0.1311', '0.2177', '-0.2585', '-0.1361', '0.0531', '0.4104', '0.2201', '-0.1816', '0.4448', '0.10016', '0.5845', '-0.2148', '0.3237', '0.3516', '0.2076', '0.0388', '0.8335', '0.332', '-0.06168', '0.893', '0.1932', '-0.0905', '-0.5146', '0.6914', '-0.05942']",,,,,,,
mondo:0015604,middle ear anomaly,,,,164004,,,,,,,,10060957,
mondo:0015605,distal monosomy 9p,"['distal deletion 9p', 'telomeric deletion 9p', 'monosomy 9pter', 'distal monosomy type 9p']",,,1642,,,,,C538025,,,,
mondo:0015606,Xp22.3 microdeletion syndrome,['Del(X)(p23)'],,,1643,CN199978,,,,,,,,
mondo:0015607,partial chromosome Y deletion,"['partial deletion of Y', 'Y-chromosome microdeletions', 'partial deletion of chromosome Y', 'partial deletion of Y chromosome short arm', 'Male sterility due to chromosome Y deletion', 'partial deletion of the long arm of the Y chromosome']",,,1646,,"['0.3225', '0.0993', '-0.2257', '-0.684', '-0.1736', '-0.623', '0.24', '0.4016', '0.03915', '-0.2288', '0.565', '-0.0886', '0.08093', '0.4656', '0.10785', '-0.4294', '-0.292', '0.0786', '-0.8735', '-0.2181', '-0.7085', '0.2462', '0.656', '-0.2598', '0.828', '-0.292', '-0.03096', '-0.547', '0.4844', '-0.1527', '0.6934', '-0.521', '0.1212', '0.006016', '-0.5425', '-0.556', '0.375', '-0.392', '-0.09467', '-0.5723', '0.727', '-0.3916', '0.05255', '-0.11365', '0.5054', '-0.4714', '-0.3784', '-0.4998', '0.361', '0.3818', '0.2076', '-0.783', '-0.5757', '0.473', '-0.368', '0.4382', '0.6143', '-0.02342', '-0.3672', '0.2439', '-0.0862', '0.008255', '0.07776', '0.2507', '0.1261', '0.3606', '0.2251', '-0.09326', '-0.1033', '0.3293', '-0.5186', '-0.2166', '-0.196', '-0.858', '-0.0973', '-0.1195', '0.4724', '-0.00887', '-0.3345', '0.713', '-0.002653', '0.5815', '-0.3936', '-0.715', '-0.2737', '-0.3118', '0.2146', '0.3008', '0.3582', '-0.1315', '-0.5957', '0.4285', '-0.7607', '0.1575', '0.918', '0.03516', '0.7207', '-0.7925', '-0.138', '-0.11993']",,,C536297,,,,
mondo:0015608,acute myeloid leukemia and myelodysplastic syndromes related to radiation,['AML and myelodysplastic syndromes related to radiation'],,,164726,CN199981,,,,,,,,
mondo:0015609,advanced sleep phase syndrome,"['familial advanced sleep-phase syndrome', 'FASPS', 'advanced sleep phase syndrome, familial', 'familial advanced sleep phase syndrome']",0050628,,164736,,"['-0.3645', '0.1886', '-0.0943', '-0.135', '0.003181', '0.02725', '0.3337', '0.2935', '-0.3628', '0.2471', '-0.2285', '-0.0141', '0.1581', '0.223', '-0.1571', '-0.265', '0.0354', '0.11395', '-0.2108', '-0.568', '-0.1616', '0.292', '0.269', '-0.3416', '-0.1366', '0.2091', '0.3337', '-0.3865', '-0.03857', '-0.1849', '0.4888', '-0.0961', '0.3774', '0.1897', '-0.3862', '0.3284', '0.014', '-0.1141', '0.2423', '-0.342', '0.421', '-0.2014', '0.3286', '-0.009636', '0.1716', '-0.625', '-0.2487', '0.7007', '-0.08234', '0.73', '-0.1536', '0.618', '-0.2179', '0.1649', '0.1362', '-0.00245', '0.1338', '-0.513', '0.0682', '-0.3772', '0.1481', '0.2117', '0.2854', '-0.4087', '-0.0414', '-0.0676', '0.4402', '0.2334', '-0.4688', '0.397', '-0.68', '0.11676', '0.0691', '0.1945', '0.10724', '0.1425', '-0.1247', '0.092', '-0.0692', '-0.2766', '0.415', '-0.0858', '0.04263', '0.3105', '0.945', '0.1969', '0.1031', '-0.051', '0.4443', '0.4526', '0.3113', '-0.1218', '-0.3623', '0.2676', '0.01285', '0.02336', '0.4207', '-0.3264', '-0.02681', '0.2297']",,,,,G47.2,,
mondo:0015610,acquired aplastic anemia,"['rare acquired aplastic anaemia', 'acquired aplastic anemia', 'rare acquired aplastic anemia']",,,164823,C0271907,,,0006926,,,,,
mondo:0015611,neutral lipid storage disease,"['Chanarin-Dorfman syndrome', 'lipidosis with triglycerid storage disease', 'lipidosis with triglyceride storage disease']",0050729,,165,CN199983,,,,,,,,
mondo:0015612,Dent disease,"['Dent syndrome', 'Dents disease', 'X-linked recessive nephrolithiasis', 'X-linked recessive hypercalciuric hypophosphatemic rickets', 'low-molecular-weight proteinuria with hypercalciuria and nephrocalcinosis', 'Dent disease 2', 'Dent disease 1', 'renal Fanconi syndrome with nephrocalcinosis and renal stones', 'Dent^s disease', 'X-linked recessive hypophosphatemic rickets']",0050699,,1652,CN239269,,C123260,,D057973,,,10069199,
mondo:0015613,dentin dysplasia,"['DD', 'dentinal dysplasia']",701,,1653,,,,,D003805,520.5,,,
mondo:0015614,dermatitis herpetiformis,"['dermatosis herpetiformis', 'Duhring^s disease', 'Durhing-Brocq disease', 'dermatitis herpetiformis']",8505,,1656,C0011608,,C26742,1000684,D003874,694.0,L13.0,10012468,
mondo:0015617,hereditary gastro-esophageal disease,['genetic gastro-esophageal disease'],,,165658,CN199993,,,,,,,,
mondo:0015619,non-syndromic urogenital tract malformation,"['nonsyndromic urogenital tract malformation', 'isolated urogenital tract malformation']",,,165704,,,,,,,,,
mondo:0015620,syndromic urogenital tract malformation,"['syndromic urogenital tract malformation', 'syndrome associated with urogenital tract malformation']",,,165707,CN226715,,,,,,,,
mondo:0015622,wound myiasis,['traumatic myiasis'],,,165955,C0344061,,,,,998.89,B87.1,,
mondo:0015623,cavitary myiasis,,,,165958,,,,,,,,,
mondo:0015624,diazoxide-sensitive diffuse hyperinsulinism,"['hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form']",,,165985,,,,,,,,,
mondo:0015625,diazoxide-resistant diffuse hyperinsulinism,"['hyperinsulinemic hypoglycemia, diazoxide-resistant diffuse form']",,,165988,,,,,,,,,
mondo:0015626,Charcot-Marie-Tooth disease,"['Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth hereditary neuropathy', 'Charcot-Marie-Tooth disease/hereditary motor and sensory neuropathy', 'CMT - Charcot-Marie-Tooth disease', 'hereditary motor and sensory neuropathy', 'Charcot Marie Tooth disease', 'CMT/HMSN', 'CMT', 'Charcot Marie Tooth muscular atrophy', 'hereditary sensorimotor neuropathy', 'peroneal muscular atrophy']",10595,,166,C0007959,"['-0.00934', '0.47', '0.0668', '0.295', '-0.0628', '0.01161', '-0.1259', '0.328', '-0.94', '-0.1615', '0.10565', '0.084', '-0.343', '0.05783', '-0.205', '-0.4023', '-0.1715', '-0.4265', '-0.363', '-0.746', '8.786e-05', '-0.08636', '0.649', '0.3584', '0.2037', '0.3945', '0.1638', '0.2732', '0.0967', '0.06235', '-0.2367', '-0.743', '0.0241', '0.229', '0.3694', '-0.7373', '-0.4841', '-0.1218', '0.65', '-0.4924', '-1.442', '-0.09503', '-0.3096', '0.67', '-0.2888', '-0.5254', '0.2292', '-0.1265', '0.073', '0.1567', '-0.03592', '0.2474', '-0.2583', '-0.8164', '0.4092', '-0.4216', '-0.0692', '0.41', '-0.733', '-0.1785', '-0.2886', '0.2338', '0.731', '0.9194', '-0.973', '0.9497', '0.05203', '0.835', '-0.659', '0.413', '-0.8604', '0.03717', '0.0387', '-0.2979', '1.138', '0.5522', '-0.325', '0.5396', '0.4011', '-0.395', '-0.0728', '0.1744', '0.4954', '0.4944', '-0.2935', '-0.4116', '-0.04895', '0.3872', '0.624', '0.35', '0.05933', '-0.3245', '0.1415', '0.634', '0.392', '0.7544', '0.4795', '-0.7095', '-0.449', '0.5566']",C75467,,D002607,356.1,,10034699,
mondo:0015627,multiple epiphyseal dysplasia due to collagen 9 anomaly,,0070305,,166002,,"['-0.5015', '-0.2915', '0.0552', '-0.2888', '0.3997', '-0.2429', '0.04446', '0.793', '-0.4502', '0.0402', '0.1731', '0.413', '-0.001701', '0.1891', '-0.1985', '-0.0349', '0.2106', '-0.05942', '-0.32', '-0.7676', '0.3591', '0.09186', '0.467', '0.00759', '-0.06885', '0.4194', '0.02492', '-0.2036', '-0.0959', '-0.1117', '0.0875', '-0.3447', '0.11755', '0.584', '0.2103', '-0.3672', '-0.1863', '-0.2744', '0.05322', '-0.1506', '-0.01175', '-0.3977', '-0.2112', '0.1232', '0.199', '-0.0878', '0.1383', '0.257', '0.0722', '-0.08826', '-0.0221', '0.2396', '0.465', '0.1575', '-0.4453', '-0.7153', '0.012726', '-0.3428', '-0.1062', '-0.1963', '0.692', '0.228', '-0.4878', '-0.04938', '-0.2766', '-0.1183', '0.4148', '0.641', '-0.177', '0.001549', '-0.3584', '-0.2377', '-0.0757', '-0.166', '0.0713', '0.471', '-0.3376', '0.3618', '-0.142', '-0.214', '-0.301', '0.0841', '0.1869', '0.2637', '-0.06177', '0.11554', '-0.1537', '0.454', '0.24', '0.00567', '-0.0784', '0.10126', '0.1038', '0.09625', '0.3135', '0.3538', '0.744', '-0.1271', '0.1807', '-0.003473']",,,,,Q77.3,,
mondo:0015628,von Willebrand disease type 2A,"['von Willebrand disease, type 2A']",,,166084,C1282968,"['-0.612', '0.4424', '-0.6084', '0.10095', '-0.03058', '-0.1674', '-0.2815', '0.4683', '-0.1133', '-0.9624', '0.4314', '0.7715', '0.4587', '0.906', '-0.1361', '-0.624', '0.1593', '0.2756', '-0.389', '-0.7305', '-0.0518', '-0.6855', '1.068', '0.4048', '0.0469', '-0.004913', '-0.1686', '-0.1058', '0.84', '0.1221', '0.8574', '-0.3433', '0.3306', '0.2278', '0.004738', '-0.3223', '-0.5796', '0.0639', '0.1132', '-0.2786', '0.4663', '0.000856', '0.1982', '-0.772', '0.2037', '-0.1974', '-0.6245', '0.134', '0.444', '-0.336', '0.739', '-0.1004', '0.4236', '-0.3608', '-0.2108', '-0.4712', '-0.685', '0.961', '-0.913', '-0.08405', '-0.5635', '0.1815', '0.599', '-0.9146', '0.2805', '-0.05515', '-0.2344', '-0.4897', '-1.051', '0.4526', '-0.1677', '-0.0954', '-0.4055', '-0.934', '0.844', '0.2047', '0.74', '0.7876', '0.2683', '0.03195', '-0.583', '-0.3298', '0.9834', '-0.4353', '-0.05698', '0.4043', '0.0673', '0.39', '0.3164', '-0.06805', '-0.6885', '0.51', '0.00279', '-0.126', '1.201', '0.5815', '0.02716', '-0.9805', '-0.4287', '0.3125']",C131686,,,,,,
mondo:0015629,von Willebrand disease type 2B,"['von Willebrand disease, type 2B']",,,166087,C1282971,"['-0.4695', '0.4116', '-0.538', '0.1584', '-0.3865', '0.04044', '-0.2269', '0.5986', '-0.03754', '-0.7715', '0.4646', '0.52', '0.5933', '0.975', '-0.1953', '-0.65', '0.1503', '0.383', '-0.1018', '-0.6353', '-0.1798', '-0.97', '1.092', '0.0979', '0.1006', '0.2429', '-0.368', '0.02342', '0.8247', '0.1304', '0.876', '-0.10736', '0.489', '0.181', '0.016', '-0.539', '-0.4277', '-0.1324', '0.1842', '-0.3394', '0.6187', '0.0331', '0.278', '-0.7666', '0.2015', '-0.4978', '-0.5874', '0.11786', '0.0202', '-0.1202', '0.718', '-0.1373', '0.02948', '-0.4294', '-0.256', '-0.496', '-0.904', '1.026', '-0.7334', '-0.0995', '-0.7485', '0.0797', '0.6177', '-0.861', '0.2213', '-0.0691', '-0.2505', '-0.586', '-1.039', '0.4683', '-0.3757', '0.0839', '-0.3586', '-1.056', '0.943', '0.2505', '0.721', '0.646', '0.603', '-0.24', '-0.844', '-0.5293', '0.94', '-0.4736', '-0.1971', '0.4043', '0.0468', '0.2556', '0.224', '-0.1835', '-0.8057', '0.506', '-0.00539', '-0.1449', '1.071', '0.4712', '0.1951', '-1.03', '-0.6406', '0.1682']",C131687,,,,,,
mondo:0015630,von Willebrand disease type 2M,"['von Willebrand disease, type 2M']",,,166090,C1282974,"['-0.3442', '0.2834', '-0.5894', '0.2607', '-0.1127', '-0.2225', '-0.343', '0.5938', '0.01243', '-0.9688', '0.4705', '0.4285', '0.5', '0.974', '0.006298', '-0.6035', '0.2085', '0.2343', '-0.2986', '-0.806', '-0.1755', '-0.8125', '1.023', '0.2888', '0.02325', '-0.02332', '-0.44', '-0.1007', '0.795', '0.197', '0.9287', '-0.284', '0.2605', '0.3835', '0.0318', '-0.3232', '-0.589', '-0.0553', '0.1855', '-0.3772', '0.5386', '-0.2014', '0.2166', '-0.7495', '0.3308', '-0.4324', '-0.5845', '0.1157', '0.3755', '-0.2878', '0.6665', '-0.02574', '0.3372', '-0.3403', '-0.1061', '-0.5938', '-0.842', '1.003', '-0.625', '-0.2998', '-0.7075', '0.2957', '0.5376', '-0.721', '0.1676', '0.1418', '-0.3086', '-0.653', '-1.078', '0.406', '-0.4453', '0.05554', '-0.249', '-1.059', '0.9023', '0.1704', '0.7', '0.77', '0.2578', '5.853e-05', '-0.7764', '-0.4429', '0.9976', '-0.6104', '-0.12445', '0.2396', '0.136', '0.3618', '0.3066', '-0.05908', '-0.767', '0.4043', '0.07874', '-0.1715', '1.099', '0.4465', '-0.10596', '-0.9834', '-0.5396', '0.3137']",C131688,,,,,,
mondo:0015631,von Willebrand disease type 2N,"['von Willebrand disease Normandy variant', 'von Willebrand disease, type 2N']",,,166093,C1282975,"['-0.4001', '0.383', '-0.538', '0.2668', '-0.1416', '0.05203', '-0.5015', '0.5776', '-0.02905', '-1.0205', '0.4668', '0.4392', '0.4744', '0.95', '0.1165', '-0.645', '0.2228', '0.08887', '-0.3105', '-0.818', '-0.2375', '-0.6733', '0.99', '0.3293', '0.03366', '-0.03537', '-0.3481', '-0.0712', '0.6704', '0.1414', '0.752', '-0.2032', '0.2559', '0.161', '-0.0521', '-0.3213', '-0.611', '-0.1853', '0.2517', '-0.4172', '0.4675', '-0.2151', '0.1235', '-0.5723', '0.4512', '-0.2805', '-0.6265', '0.1846', '0.3064', '-0.2615', '0.721', '0.00776', '0.1881', '-0.2357', '-0.12006', '-0.5337', '-0.8457', '0.959', '-0.7114', '-0.2764', '-0.5156', '0.1378', '0.4302', '-0.6167', '0.07965', '-0.04297', '-0.323', '-0.6465', '-1.172', '0.3787', '-0.3118', '0.03836', '-0.1439', '-0.881', '0.875', '0.309', '0.6973', '0.8525', '0.2832', '0.1283', '-0.703', '-0.403', '0.8955', '-0.4116', '-0.05365', '0.3115', '0.0426', '0.34', '0.1152', '-0.05533', '-0.531', '0.3074', '-0.02095', '-0.1681', '1.173', '0.5996', '-0.001792', '-0.876', '-0.4114', '0.2394']",C131689,,,,,,
mondo:0015632,FASTKD2-related infantile mitochondrial encephalomyopathy,,,,166105,,,,,,,,,
mondo:0015634,isolated osteopoikilosis,['nonsyndromic osteopoikilosis (disease)'],,,166119,,"['-0.2944', '0.075', '-0.1046', '-0.5063', '0.1378', '-0.02103', '-0.2832', '0.3052', '-0.376', '-0.02422', '-0.04544', '0.383', '0.0586', '0.0596', '0.0348', '0.317', '0.05643', '-0.052', '-0.02075', '-0.604', '0.02563', '0.02226', '0.6553', '0.0653', '0.263', '0.3665', '0.3008', '-0.0793', '0.06586', '0.4531', '0.11566', '-0.542', '0.01173', '0.237', '0.3718', '0.008415', '-0.1334', '-0.357', '0.1367', '-0.3857', '0.1671', '-0.601', '0.2744', '-0.1794', '-0.095', '-0.2505', '-0.3877', '0.2438', '0.14', '-0.1277', '0.4385', '0.007465', '-0.02684', '0.4214', '-0.3713', '-0.2861', '0.04315', '0.0769', '-0.3127', '0.1608', '0.4773', '0.11426', '-0.496', '-0.2917', '-0.04642', '-0.03513', '0.3992', '0.3926', '0.09625', '0.61', '0.0639', '-0.4282', '0.10486', '-0.1571', '-0.01437', '0.0663', '-0.2108', '0.3718', '-0.1711', '-0.469', '-0.0581', '0.1183', '0.2566', '0.02458', '-0.3691', '-0.183', '-0.1559', '0.1492', '0.2006', '4.6e-05', '-0.06946', '0.1077', '0.04486', '0.3142', '0.6274', '0.1862', '0.1902', '-0.3506', '0.139', '0.1802']",,,,,,,
mondo:0015635,porokeratotic eccrine ostial and dermal duct nevus,"['linear eccrine Nevus with comedones', 'Porokeratotic eccrine duct and hair follicle Nevus', 'Porokeratotic eccrine nevus', 'comedo nevus of the palm']",,,166286,C0473579,,C4740,,,,,,
mondo:0015636,dirofilariasis,"['Dirofilaria caused disease or disorder', 'infection by Dirofilaria', 'Dirofilaria infectious disease']",1082,,166291,C0012602,,,0007239,D004184,125.6,,,
mondo:0015637,benign non-familial infantile seizures,,,,166295,CN226716,,,,,,,,
mondo:0015638,benign partial epilepsy of infancy with complex partial seizures,,,,166299,CN226717,,,,,,,,
mondo:0015639,benign partial epilepsy with secondarily generalized seizures in infancy,,,,166302,CN226718,,,,,,,,
mondo:0015640,benign infantile seizures associated with mild gastroenteritis,,,,166305,,,,,,,,,
mondo:0015641,benign infantile focal epilepsy with midline spikes and wave during sleep,"['benign infantile focal epilepsy with midline spikes and waves during sleep', 'BIMSE']",,,166308,,,,,,,,,
mondo:0015642,benign partial infantile seizures,,,,166311,,,,,,,,,
mondo:0015643,photosensitive epilepsy,"['photogenic epilepsy', 'photoparoxysmal response', 'PSE']",0060281,,166409,C0393720,,,,,345.80,,,
mondo:0015644,audiogenic seizures,,,,166415,C0751791,,,,,,,,
mondo:0015645,eating seizures,"['eating reflex epilepsy', 'eating epilepsy']",,,166418,C0393725,,,,,,,,
mondo:0015646,orgasm-induced seizures,,,,166421,CN200056,,,,,,,,
mondo:0015647,thinking seizures,,,,166424,CN200057,,,,,,,,
mondo:0015648,startle epilepsy,,,,166427,CN200058,,,,,,,,
mondo:0015649,micturation-induced seizures,,,,166430,CN200059,,,,,,,,
mondo:0015650,epilepsy syndrome,"['syndromic epilepsy', 'epileptic syndrome']",,,166463,,,,,,,,,
mondo:0015653,monogenic epilepsy,['monogenic disease with epilepsy'],,,166472,CN200063,,,,,,,,
mondo:0015660,sporadic fetal brain disruption sequence,,,,1665,CN237425,,,,,,,,
mondo:0015661,dextrocardia,"['dextrocardia (disease)', 'dextrocardia', 'heart predominantly in right hemithorax']",9565,,1666,,,C84669,,D003914,746.87,,10012592,0001651
mondo:0015663,diencephalic syndrome,"['Russell diencephalic cachexia', 'diencephalic syndrome of childhood', 'diencephalic syndrome of infancy', 'diencephalic syndrome of emaciation', 'diencephalic cachexia', 'Russell syndrome']",,,1672,CN200089,,C116955,,,253.8,,,
mondo:0015664,idiopathic pulmonary artery dilatation,['idiopathic dilatation of the pulmonary artery'],,,1676,,,,,,,,,
mondo:0015665,scleromyxedema,"['generalised papular and sclerodermoid lichen myxedematosus', 'generalized papular and sclerodermoid lichen myxedematosus', 'scleromyxoedema', 'generalised papular and sclerodermoid', 'generalized papular and sclerodermoid', 'myxedematosus, lichen', 'papular mucinosis', 'generalized lichenoid papular eruption', 'Scleromyxedema', 'generalised lichenoid papular eruption', 'mucinosis, papular', 'Arndt-Gottron disease', 'lichen myxedematosus']",,,167635,CN200092,,C85061,,D053718,701.8,,10055046,
mondo:0015666,familial idiopathic dilatation of the right atrium,['familial idiopathic dilatation of the right atrium (disease)'],,,1677,CN200093,,,,,,,,
mondo:0015667,acute myeloid leukemia by FAB classification,"['unclassified AML', 'acute myeloid leukemia, NOS', 'acute myeloid leukemia not otherwise specified', 'acute myeloid leukemia not otherwise categorized', 'AML, NOS', 'acute myeloid leukaemia not otherwise specified', 'acute myeloid leukaemia NOS', 'unclassified acute myeloid leukaemia', 'acute myeloid leukemia NOS', 'unclassified acute myeloid leukemia', 'acute myeloid leukemia', 'acute myeloid leukaemia', 'acute myeloid leukaemia not otherwise categorised']",,,167714,,,C27753,,,,,,
mondo:0015668,hereditary dentin defect,,,,167759,,,,,,,,,
mondo:0015672,diprosopus,"['craniofacial duplication', 'Diprosopia']",,,1681,,,,,,,,,
mondo:0015674,late infantile neuronal ceroid lipofuscinosis,"['Jansky-Bielschowsky disease', 'LINCL', 'late infantile NCL']",,,168491,,"['-0.0304', '-0.04187', '0.063', '0.2769', '0.1698', '-0.85', '0.02623', '0.798', '-0.3857', '-0.523', '-1.086', '-0.1929', '-0.1304', '0.359', '0.3074', '-0.7285', '-0.482', '-0.2109', '-0.07043', '-0.3516', '-0.103', '-0.543', '0.4275', '-0.07806', '-0.2778', '-0.4722', '-0.3306', '0.543', '-0.6606', '0.01889', '0.491', '-0.1431', '0.001578', '-0.10284', '0.0746', '0.4702', '-0.3628', '-0.1282', '-0.525', '0.12006', '0.2083', '-0.578', '0.1812', '-0.0809', '0.3728', '-0.2015', '-0.001957', '-0.2135', '0.02942', '0.4705', '0.4893', '0.242', '-0.835', '-0.4858', '0.6655', '-0.546', '0.305', '-0.3203', '-0.1942', '0.2313', '-0.1637', '-0.1873', '0.3604', '0.2756', '-0.00723', '0.417', '0.3777', '0.2651', '-0.2295', '-0.146', '0.07465', '-0.509', '-0.116', '-0.03235', '0.4543', '-0.09906', '0.1244', '-0.3025', '-0.2488', '-0.2666', '0.3044', '-0.1794', '-0.3027', '0.911', '0.1958', '-0.4275', '0.1086', '0.2546', '0.335', '-0.10645', '0.6426', '-0.0397', '-0.4985', '0.4485', '0.389', '0.2644', '0.4329', '-0.734', '0.3127', '-0.1384']",,,,,,,
mondo:0015675,distomatosis,"['fluke infection', 'distomiasis']",,,1685,,,,,,121.9,,,
mondo:0015677,cardiac diverticulum,"['Cardiac diverticulum', 'cardiac diverticulum (disease)']",,,1686,CN226726,,,,,,,,0100571
mondo:0015678,"dysplasia of head of femur, Meyer type",,,,168621,C4274970,,,,,,,,
mondo:0015679,autosomal thrombocytopenia with normal platelets,,,,168629,CN200175,"['-0.1048', '0.1148', '6.52e-05', '-0.02919', '0.0914', '-0.0456', '-0.001409', '0.1776', '-0.02608', '-0.1284', '-0.01852', '-0.0367', '0.0341', '-0.001847', '-0.02023', '-0.02719', '-0.0516', '-0.000589', '-0.0379', '-0.2177', '-0.00995', '-0.0458', '0.1512', '-0.0502', '0.0765', '-0.02219', '-0.03156', '-0.01808', '0.03125', '-0.01065', '0.08777', '-0.02017', '0.1299', '0.0883', '-0.03903', '-0.04706', '-0.0841', '-0.0663', '0.003042', '-0.168', '0.00646', '-0.0666', '0.06204', '-0.0816', '-0.05026', '-0.1569', '-0.03937', '0.0675', '0.0698', '-0.0264', '0.01979', '-0.02525', '0.09064', '0.01988', '-0.07477', '-0.02982', '0.08325', '-0.1051', '-0.1709', '-0.0186', '0.10986', '0.03235', '0.02399', '-0.01862', '-0.003426', '-0.07434', '0.1102', '0.1133', '-0.0978', '0.2136', '-0.1215', '-0.02324', '-0.03113', '-0.11066', '0.081', '0.05063', '0.0512', '-0.03192', '-0.0245', '-0.0763', '-0.0646', '-0.03308', '0.01266', '0.05966', '-0.05234', '0.0204', '0.04745', '0.1388', '0.0754', '0.0006924', '0.07166', '0.1428', '-0.0158', '0.06195', '0.2188', '0.1614', '0.0834', '-0.2439', '-0.0211', '0.0564']",,,,,,,
mondo:0015681,childhood disintegrative disorder,"['disintegrative psychosis', 'childhood disintegrative disease', 'heller syndrome', 'symbiotic psychosis', 'dementia infantilis', 'heller^s syndrome']",13487,,168782,CN072151,,C97164,,,299.1,,10008522,
mondo:0015682,primary peritoneal tumor,,,,168803,CN200180,,,,,,,,
mondo:0015683,primary malignant peritoneal tumor,,,,168807,CN200181,,,,,,,,
mondo:0015686,primary peritoneal carcinoma,"['EOPPC', 'Extra-ovarian primary peritoneal carcinoma', 'PPC', 'primary peritoneal cancer', 'primary peritoneal carcinoma (disease)', 'primary peritoneal serous carcinoma', 'serous surface papillary carcinoma', 'primary peritoneal carcinoma']",,,168829,CN200184,,C40022,,,,,,0030406
mondo:0015687,chronic eosinophilic leukemia,"['CEL/hypereosinophilic syndrome', 'chronic eosinophilic leukemia', 'CEL', 'CELNOS', 'chronic eosinophilic leukemia/hypereosinophilic syndrome', 'eosinophilic leukemia', 'eosinophilic leukaemia']",0080367,,168940,C0346421,,C4563,1000178,C580364,,,10065854,
mondo:0015688,"myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2","['myeloid and lymphoid neoplasms with eosinophilia and rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2', 'myeloid/lymphoid neoplasms with eosinophilia and rearrangement of PDGFRA, PDGFRB, or FGFR1, or with PCM1-JAK2', 'myeloid/lymphoid neoplasms with eosinophilia and gene rearrangement', 'myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, or FGFR1', 'myeloid/lymphoid neoplasms associated with eosinophilia and abnormality of PDGFRA, PDGFRB, FGFR1 or JAK2', 'myeloid and lymphoid neoplasms with eosinophilia and abnormalities of platelet-derived growth factor receptor alpha (PDGFRA), platelet-derived growth factor receptor beta (PDGFRB), and fibroblast growth factor receptor-1 (FGFR1) are a group of hematologic neoplasms', 'myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1']",0080164,,168943,C2827356,,C84270,,,,,,
mondo:0015689,myeloid neoplasm associated with PDGFRA rearrangement,"['myeloid and lymphoid neoplasms with PDGFRA rearrangement', 'myeloid/lymphoid neoplasm associated with PDGFRA rearrangement', 'myeloid and lymphoid neoplasms associated with PDGFRA rearrangement', 'myeloid/lymphoid neoplasms with PDGFRA rearrangement']",0080165,,168947,C4545381,,C84275,,,,,,
mondo:0015690,myeloid neoplasm associated with PDGFRB rearrangement,"['myeloid neoplasms associated with PDGFRB rearrangement', 'myeloid and lymphoid neoplasms with PDGFRB rearrangement', 'myeloid neoplasms with PDGFRB rearrangement', 'myeloid/lymphoid neoplasms with PDGFRB rearrangement', 'myeloid/lymphoid neoplasm associated with PDGFRB rearrangement']",0080166,,168950,C2827361,,C84276,,,,,,
mondo:0015691,hypereosinophilic syndrome,"['hypereosinophilic syndrome', 'HES', 'eosinophilia', 'eosinophilic leukocytosis']",999,,168956,C1540912,,C27038,1001467,D017681,288.3,,10048643,
mondo:0015692,refractory anemia with excess blasts in transformation,['RAEB-t'],,,168960,CN200189,,C27080,,,238.73,,10038271,
mondo:0015694,malignant melanoma of the mucosa,['mucosa melanoma (disease)'],,,168999,CN200193,,,,,,,,
mondo:0015695,combined immunodeficiency due to CRAC channel dysfunction,['immune dysfunction due to T-cell inactivation due to calcium entry defect'],,,169090,,"['0.03836', '0.08997', '0.2734', '-0.664', '0.691', '-0.1785', '0.2198', '0.3586', '0.11755', '-0.578', '0.2042', '-0.06287', '-1.06', '-0.3875', '0.2964', '-0.2754', '-0.2754', '-0.6577', '-0.2874', '-0.751', '-0.05566', '-0.10376', '0.786', '-0.505', '-0.3015', '0.231', '-0.808', '-0.1803', '-0.662', '-0.6694', '-0.667', '0.295', '-0.1372', '0.4214', '-0.007706', '-0.2178', '-0.337', '0.361', '-0.615', '-0.0444', '-0.58', '-0.0727', '0.1943', '-0.2001', '-0.56', '0.6646', '0.05478', '0.1522', '0.7666', '0.17', '-0.3596', '-0.2487', '0.6953', '0.318', '0.0863', '-0.5615', '0.6587', '-0.2118', '0.06616', '0.1422', '0.3538', '0.4548', '-0.02766', '-0.2744', '0.12244', '-0.3135', '0.1823', '0.449', '-0.2734', '0.5527', '-0.5586', '-0.1566', '0.1584', '-0.5474', '0.657', '-0.2566', '0.5703', '-0.1157', '-0.2842', '0.696', '-0.076', '0.368', '0.333', '0.3845', '-0.1428', '0.9175', '0.8613', '0.837', '0.6514', '0.1826', '0.02232', '0.5864', '0.2233', '0.2812', '0.8633', '1.249', '0.1948', '0.04367', '0.3372', '0.1453']",,,,,,,
mondo:0015696,Good syndrome,"['thymoma with hypogammaglobulinemia', 'immunodeficiency with thymoma', 'thymoma-immunodeficiency syndrome']",0060028,,169105,C0221027,,,,,,,,
mondo:0015697,immunoglobulin heavy chain deficiency,,,,169110,C0398692,,,,,279.03,,,
mondo:0015698,transient hypogammaglobulinemia of infancy,"['transient hypogammaglobulinemia of infancy', 'THI']",624,,169139,C0272238,,C27071,,,279.09,D80.7,10044388,
mondo:0015699,immunodeficiency due to a classical component pathway complement deficiency,"['immunodeficiency due to a C1, C4, or C2 component complement deficiency', 'immunodeficiency due to C1, C4, or C2 component complement deficiency', 'immunodeficiency due to an early component of complement deficiency']",,,169147,,,,,,,,,
mondo:0015700,immunodeficiency due to a late component of complement deficiency,"['immunodeficiency due to C5 to C9 component complement deficiency', 'immunodeficiency due to a C5 to C9 component complement deficiency', 'deficiency of complement of terminal pathway', 'terminal complement pathway deficiency']",,,169150,,"['-0.3782', '-0.0604', '-0.2334', '0.00528', '0.057', '-0.0838', '0.2817', '-0.3982', '-0.2189', '-0.2349', '-0.0196', '0.1469', '-0.307', '0.0004785', '0.1315', '-0.1328', '-0.3867', '-0.2444', '-0.3438', '-0.5083', '0.3323', '-0.1873', '0.855', '-0.05823', '0.3179', '0.01214', '-0.3354', '0.0911', '-0.1572', '-0.1043', '0.253', '0.269', '0.1571', '0.1888', '0.269', '-0.04666', '-0.03687', '0.114', '-0.2126', '-0.3809', '0.0463', '0.09906', '0.3691', '-0.10205', '-0.0866', '-0.6426', '0.010605', '-0.2952', '0.2705', '0.4988', '-0.05753', '-0.0734', '0.2954', '-0.1885', '-0.594', '-0.0257', '0.3481', '-0.409', '-0.3123', '0.005474', '-0.2157', '0.1726', '0.259', '0.3086', '0.5396', '0.4788', '0.5312', '0.1965', '-0.1008', '0.3667', '-0.2445', '-0.1183', '0.06366', '-0.1476', '-0.0004675', '-0.1117', '0.5366', '0.5176', '0.1137', '0.00784', '-0.4014', '0.005257', '0.1317', '0.2686', '0.04657', '-0.3618', '0.4355', '0.2212', '0.1945', '-0.02147', '0.2788', '0.2201', '0.0713', '-0.369', '0.5737', '0.5547', '0.1345', '-0.4524', '-0.119', '0.01512']",,,,,,,
mondo:0015701,T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiency,"['T-B+ SCID due to IL-7Ralpha deficiency', 'IL-7R', 'interleukin-7 receptor alpha deficiency']",0060015,,169154,C1837028,,,,,,,,
mondo:0015702,T-B+ severe combined immunodeficiency due to CD45 deficiency,"['T-B+ SCID due to CD45 deficiency', 'CD45 deficiency']",0060014,,169157,C1837028,,,,,,,,
mondo:0015703,T-B+ severe combined immunodeficiency due to CD3delta/CD3epsilon/CD3zeta,['T-B+ SCID due to CD3delta/CD3epsilon/CD3zeta'],,,169160,,,,,,,,,
mondo:0015704,familial scaphocephaly syndrome,,,,169163,,,,,,,,10072229,
mondo:0015705,autosomal recessive centronuclear myopathy,"['AR-CNM', 'centronuclear myopathy, autosomal recessive']",0111216,,169186,C3645536,"['-0.259', '-0.4587', '-0.5293', '0.02913', '0.197', '-0.64', '0.269', '0.7046', '-1.023', '-0.2402', '-0.2363', '-0.0993', '0.04135', '0.11224', '-0.009995', '0.5854', '-0.1265', '-0.142', '-0.638', '-1.145', '0.1054', '-0.02617', '0.503', '0.393', '-0.0321', '-0.261', '-0.02153', '0.02507', '0.02863', '0.1431', '0.715', '0.011696', '-0.1903', '-0.04782', '-0.2239', '-0.1842', '-0.529', '-0.2646', '0.5884', '-0.2878', '-0.2517', '-0.193', '0.2316', '0.338', '0.503', '-0.2976', '0.04092', '0.2089', '-0.2693', '0.01813', '-0.4722', '-0.01044', '-0.057', '-0.3486', '-0.1138', '-0.6777', '0.4106', '0.02588', '-0.2448', '-0.2185', '0.05792', '-0.1943', '-0.1472', '0.1492', '-0.4448', '0.0738', '0.1934', '0.4216', '-0.3645', '0.4468', '-0.724', '-0.1168', '0.1553', '0.8047', '0.5444', '-0.3662', '0.2896', '-0.2197', '-0.0724', '-0.321', '0.508', '0.07605', '0.4307', '0.999', '-0.010864', '0.7334', '-0.02489', '0.488', '-0.01426', '-0.0639', '0.06024', '0.2476', '0.3315', '-0.0879', '0.643', '0.1628', '0.9116', '0.2012', '-0.349', '-0.1774']",,,,,,,
mondo:0015706,mosaic trisomy 1,"['trisomy 1 mosaicism', 'Mosaic trisomy type 1', 'Mosaic trisomy chromosome 1']",,,1692,CN073987,,,,,,,,
mondo:0015708,immuno-osseous dysplasia,,,,169349,,,,,,,,,
mondo:0015712,non-distal trisomy 10q,"['non-telomeric trisomy 10q', 'non-distal duplication 10q', 'non-distal trisomy type 10q']",,,1695,,,,,,,,,
mondo:0015713,idiopathic central precocious puberty,,,,169615,C0342544,,C120372,,,259.1,,,
mondo:0015714,secondary central precocious puberty,,,,169618,CN200226,,,,,,,,
mondo:0015715,severe hemophilia B,"['severe factor IX deficiency', 'severe haemophilia type B', 'severe hemophilia type B']",,,169793,CN200227,,,,,,,,
mondo:0015716,moderately severe hemophilia B,"['moderately severe haemophilia type B', 'moderately severe factor IX deficiency', 'moderately severe hemophilia type B']",,,169796,CN200228,,,,,,,,
mondo:0015717,mild hemophilia B,"['mild haemophilia type B', 'mild hemophilia type B', 'mild factor IX deficiency']",,,169799,CN200229,,,,,,,,
mondo:0015718,mosaic trisomy 12,"['Mosaic trisomy type 12', 'Mosaic trisomy chromosome 12', 'trisomy 12 mosaicism']",,,1698,CN073989,,,,,,,,
mondo:0015719,severe hemophilia A,"['severe factor VIII deficiency', 'severe haemophilia type A', 'severe hemophilia type A']",,,169802,C0272322,,,,,,,,
mondo:0015720,moderately severe hemophilia A,"['moderately severe hemophilia type A', 'moderately severe factor VIII deficiency', 'moderately severe haemophilia type A']",,,169805,CN200231,,,,,,,,
mondo:0015721,mild hemophilia A,"['mild haemophilia type A', 'mild factor VIII deficiency', 'mild hemophilia type A']",,,169808,C0272324,,,,,,,,
mondo:0015722,congenital vitamin K-dependent coagulation factors deficiency,"['vitamin K-dependent clotting factors, combined deficiency of', 'congenital vitamin K-dependent coagulation factors combined deficiency']",0112172,,98434,,"['0.11383', '-0.08', '-0.4883', '-0.2815', '0.3872', '0.198', '0.0782', '0.2494', '-0.2927', '-0.632', '-0.8105', '0.0236', '0.632', '0.7534', '-0.4158', '-0.3835', '0.0757', '-0.1829', '-0.2273', '-0.6636', '0.431', '-0.5347', '0.873', '0.0996', '-0.3694', '0.02376', '0.1693', '0.04846', '0.4734', '-0.2725', '0.1337', '0.2109', '0.4631', '0.08026', '0.1525', '-0.403', '0.05597', '-0.564', '0.2352', '0.206', '0.2416', '-0.4763', '0.01445', '0.2598', '0.3218', '-0.666', '-0.1549', '-0.03436', '0.2435', '0.00558', '-0.00281', '-0.8276', '0.403', '0.12317', '-0.606', '-0.05185', '0.05997', '-0.05176', '-0.06525', '0.671', '-0.421', '-0.1913', '0.4507', '0.1056', '-0.0878', '0.124', '0.2205', '0.239', '-0.04346', '-0.1799', '0.02815', '-0.372', '-0.5312', '0.0684', '0.44', '0.683', '0.7505', '0.483', '0.447', '-0.446', '-0.1071', '0.5566', '0.1765', '0.1289', '0.0771', '0.426', '-0.399', '0.5376', '0.443', '-0.2876', '0.4521', '0.6196', '-0.191', '-0.536', '0.3218', '0.1979', '0.0385', '-0.6953', '0.07416', '0.2451']",,,,,,,
mondo:0015723,trisomy 12p,"['chromosome 12p duplication', 'partial trisomy 12p', 'trisomy type 12p', '12p trisomy', 'Duplication 12p', '12p duplication']",,,1699,C0795845,,,,C538299,,,,
mondo:0015724,non-distal trisomy 13q,"['non-distal trisomy type 13q', 'non-distal duplication 13q', 'non-telomeric trisomy 13q']",,,1702,,,,,,,,,
mondo:0015725,mosaic trisomy 14,"['Mosaic trisomy chromosome 14', 'trisomy 14 mosaicism', 'Mosaic trisomy type 14']",,,1703,C2930917,,C116319,,C535489,,,,
mondo:0015726,distal trisomy 14q,"['telomeric duplication 14q', 'distal duplication 14q', 'trisomy 14qter', 'distal trisomy type 14q']",,,1705,CN036934,,,,C538034,,,,
mondo:0015727,mosaic trisomy 15,"['chromosome 15, trisomy mosaicism', 'Mosaic trisomy type 15', 'Mosaic trisomy chromosome 15', 'trisomy 15 mosaicism']",,,1706,CN035788,,,,C538037,,,,
mondo:0015728,distal trisomy 15q,"['telomeric duplication 15q', 'distal duplication 15q', 'distal trisomy type 15q', 'trisomy 15qter']",,,1707,,,,,C538036,,,,
mondo:0015729,mosaic trisomy 16,"['Mosaic trisomy chromosome 16', 'trisomy 16 mosaicism', 'Mosaic trisomy type 16']",,,1708,,,,,C538041,,,,
mondo:0015730,mosaic trisomy 17,"['trisomy 17 mosaicism', 'chromosome 17 duplication', 'chromosome 17 trisomy', 'Mosaic trisomy chromosome 17', 'chromosome 17, trisomy', 'trisomy 17', 'chromosome 17, trisomy mosaicism', 'Mosaic trisomy type 17']",,,1711,C1096168,,C37865,,C538044,,,,
mondo:0015731,high anorectal malformation,,,,171201,,,,,,751.5,,,
mondo:0015732,intermediate anorectal malformation,,,,171208,,,,,,,,,
mondo:0015733,low anorectal malformation,,,,171215,C0345218,,C98975,,,751.5,,,
mondo:0015734,rectal duplication,,,,171220,,,,,,,,,
mondo:0015735,severe congenital nemaline myopathy,['severe congenital (neonatal) NM'],,,171430,,,,,,,,,
mondo:0015736,intermediate nemaline myopathy,"['Intermediate congenital NM', 'Intermediate congenital nemaline myopathy']",,,171433,,,,,,,,,
mondo:0015737,typical nemaline myopathy,['typical congenital nemaline myopathy'],,,171436,,,,,,,,,
mondo:0015738,childhood-onset nemaline myopathy,['mild nemaline myopathy'],,,171439,,,,,,,,,
mondo:0015739,adult-onset nemaline myopathy,,,,171442,C0546123,,,,,,,,
mondo:0015740,trisomy 18p,"['18p trisomy', 'trisomy type 18p', 'Duplication 18p', 'chromosome 18p duplication', '18p duplication', 'partial trisomy 18p', 'Duplication of the short arm of chromosome 18', 'trisomy of the short arm of chromosome 18']",,,1715,,,,,C538307,,,,
mondo:0015741,distal trisomy 18q,"['telomeric duplication 18q', 'distal trisomy type 18q', 'trisomy 18qter', 'distal duplication 18q']",,,1716,,,,,,,,,
mondo:0015742,periventricular leukomalacia,['PVL'],13088,,171676,C0023529,,C99013,1001101,D007969,779.7,,10052594,
mondo:0015743,idiopathic bilateral vestibulopathy,,,,171684,C4545229,,,,,,,,
mondo:0015744,distal trisomy 19q,"['telomeric duplication 19q', 'trisomy 19qter', 'distal trisomy type 19q', 'distal duplication 19q']",,,1717,,,,,,,,,
mondo:0015745,microcephaly-polymicrogyria-corpus callosum agenesis syndrome,,,,171703,CN200295,,,,,,,,
mondo:0015746,male infertility due to globozoospermia,"['globozoospermia', 'male infertility due to round-headed spermatozoa', 'Male infertility due to round-headed spermatozoa', 'round-headed sperm syndrome', 'male infertility due to globozoospermia']",0112312,,171709,,"['-0.682', '-0.6694', '0.09186', '-0.542', '-0.348', '-0.445', '-0.0726', '0.651', '-0.535', '-0.528', '1.561', '-0.0611', '-0.1881', '1.034', '-0.05548', '-0.1833', '-0.005276', '0.6206', '-0.4531', '-1.126', '-0.2102', '0.185', '0.4988', '-0.3452', '0.441', '-0.7173', '0.3167', '0.0422', '-0.655', '-0.5186', '0.5747', '-0.1854', '-0.4187', '-0.1043', '0.1742', '0.02574', '-0.08813', '-0.0407', '0.167', '-0.161', '0.136', '0.4175', '0.1478', '-0.2964', '0.7754', '-0.7344', '0.3423', '-0.892', '0.66', '0.4624', '-0.6323', '-0.2876', '-0.0703', '0.637', '-0.1167', '0.631', '0.299', '0.1038', '-0.7397', '0.156', '0.2107', '0.905', '-0.1698', '0.1188', '-0.2593', '0.4802', '0.03244', '0.69', '-1.121', '0.8213', '-0.396', '0.1658', '-0.1002', '-0.1349', '0.1019', '0.567', '0.571', '0.4316', '-0.2467', '0.29', '0.0647', '0.2583', '0.145', '-0.717', '-0.0849', '-0.815', '0.2207', '9.596e-05', '0.4236', '-0.6875', '-0.494', '0.486', '-0.6978', '1.125', '0.539', '-0.4097', '0.2705', '-0.4468', '-0.9087', '-0.00988']",,,,,,,
mondo:0015748,hereditary mucosal leukokeratosis,"['white sponge nevus of Cannon', 'hereditary mucosal leukokeratosis', 'white sponge nevus', 'White sponge nevus of Cannon']",0050448,,171723,C1721005,"['-0.0722', '0.2805', '-0.04398', '-0.03102', '0.4229', '-0.2698', '-0.3936', '0.1636', '-0.3843', '-0.11304', '-0.1891', '-0.3606', '-0.3735', '-0.1423', '-0.2161', '0.11127', '-0.0763', '-0.4846', '-0.2239', '-0.2717', '-0.148', '-0.2756', '0.1997', '-0.3552', '0.4048', '0.2284', '-0.1586', '0.1921', '0.1617', '-0.458', '0.4438', '0.04758', '-0.3398', '0.1809', '0.3428', '0.3264', '-0.1938', '-0.02061', '0.2012', '-0.2103', '0.0699', '-0.3152', '0.006115', '0.0262', '-0.1682', '-0.2844', '0.0798', '0.2494', '0.3188', '-0.1765', '0.03044', '-0.2482', '0.11115', '-0.1719', '-0.51', '-0.1608', '0.5693', '0.3665', '-0.4656', '0.02133', '0.001541', '-0.0373', '-0.351', '-0.0511', '0.243', '0.06635', '0.4363', '0.1353', '0.168', '0.6143', '0.138', '-0.2817', '-0.1809', '-0.0339', '0.06934', '0.1111', '0.0616', '0.3123', '-0.157', '-0.5264', '-0.03009', '-0.272', '0.2245', '0.05173', '-0.1444', '-0.143', '-0.3215', '0.2354', '-0.01788', '-0.02412', '-0.2318', '0.01715', '0.2588', '0.126', '0.6797', '-0.03702', '0.344', '-0.3574', '-0.05484', '0.1958']",C84760,,D053529,528.6,,,
mondo:0015749,6q16 deletion syndrome,"['Del(6)(q16)', 'monosomy 6q16', 'Prader-Willi-like syndrome due to deletion 6q16']",,,171829,CN200301,,,,,,,,
mondo:0015751,craniosynostosis-hydrocephalus-Arnold-Chiari malformation type I-radioulnar synostosis syndrome,"['Berant syndrome', 'familial scaphocephaly-radioulnar synostosis syndrome', 'Capra-DeMarco syndrome']",,,171839,C3267187,,,,,,,,
mondo:0015752,intellectual disability-cataracts-kyphosis syndrome,,,,171860,CN226733,,,,,,,,
mondo:0015753,cap myopathy,"['congenital myopathy with caps', 'Cap disease']",,,171881,C3710589,,,,C579969,,,,
mondo:0015755,myopathy with hexagonally cross-linked tubular arrays,,,,171889,,,,,,,,,
mondo:0015756,myeloid hemopathy,,,,171895,,,,,,,,,
mondo:0015757,lymphoid hemopathy,,,,171898,,,,,,,,,
mondo:0015758,primary cutaneous T-cell lymphoma,,,,171901,,,,,D016410,,,10011677,
mondo:0015759,B-cell non-Hodgkin lymphoma,"['B-cell non-Hodgkin^s lymphoma', 'lymphomas non-Hodgkin^s B-cell', 'B-cell NHL', 'non-Hodgkin^s B-cell lymphoma', 'B-cell non Hodgkin^s lymphoma', 'B-cell non-Hodgkin lymphoma', 'non-Hodgkin^s lymphoma B-cell', 'B-cell lymphoma']",,,171915,,,C3457,,,,,,
mondo:0015760,T-cell non-Hodgkin lymphoma,"['T-cell lymphoma', 'T cell lymphoma', 'T-cell and NK-cell non-Hodgkin lymphoma', 'T-cell non-Hodgkin^s lymphoma', 'T-cell NHL', 'T-cell non-Hodgkin lymphoma', 'non-Hodgkin^s T-cell lymphoma', 'T-cell and NK-cell non-Hodgkin^s lymphoma']",0081312,,171918,C0079772,,C3466,,D016399,202.70,,10042971,
mondo:0015761,trisomy 10p,"['Duplication 10p', 'partial trisomy 10p', 'chromosome 10p duplication', '10p trisomy', 'trisomy type 10p', '10p duplication']",,,171929,C4082793,,,,C538290,,,,
mondo:0015762,progressive familial intrahepatic cholestasis,"['PFIC', 'cholestasis, progressive familial intrahepatic']",0070221,,172,C0268312,"['0.1675', '0.335', '-0.0599', '0.0985', '-0.1288', '-0.3142', '0.2778', '0.5327', '-0.012054', '0.0786', '-0.3767', '-0.2395', '-0.4175', '0.552', '-0.2554', '-0.083', '0.0619', '-0.3052', '0.01923', '-0.9673', '-0.362', '-0.3247', '0.5005', '0.07806', '0.10956', '0.2344', '-0.0461', '0.518', '-0.5537', '-0.639', '0.6284', '-0.03406', '-0.05276', '0.326', '-0.4302', '-0.05725', '-0.6025', '-0.185', '-0.1694', '0.3809', '-0.2046', '-0.3625', '0.649', '0.4136', '-0.0186', '-0.1901', '0.3926', '-0.4563', '0.3247', '-0.3264', '-0.1306', '0.08453', '0.05548', '-0.3896', '0.2317', '-0.2087', '0.657', '0.2328', '-0.4888', '0.661', '0.665', '0.06223', '0.3794', '-0.0465', '-0.02274', '-0.2085', '0.9224', '0.2089', '-0.1669', '0.4001', '-0.2866', '-0.425', '0.06192', '-0.1779', '0.7896', '0.16', '0.1204', '0.00861', '0.0542', '-0.05075', '0.2141', '0.2998', '-0.4124', '-0.0952', '-0.538', '0.0956', '0.444', '-0.516', '0.2815', '-0.4387', '0.4075', '0.0923', '-0.4155', '0.08484', '0.4146', '0.1521', '0.3538', '-0.38', '-0.1824', '-0.3416']",C84453,,,,,,
mondo:0015763,mosaic trisomy 2,"['Mosaic trisomy chromosome 2', 'trisomy 2 mosaicism', 'Mosaic trisomy type 2']",,,1723,CN073991,,,,,,,,
mondo:0015764,mosaic trisomy 20,"['Mosaic trisomy type 20', 'Mosaic trisomy chromosome 20']",,,1724,,,,,,,,,
mondo:0015765,congenital myopathy with cores,,,,172976,,,,,,,,,
mondo:0015766,cholera,"['cholera - Vibrio cholerae', 'Vibrio cholerae caused disease or disorder', 'Vibrio cholerae', 'cholera due to Vibrio cholerae', 'Vibrio cholerae infection']",1498,,173,C0008354,,C157812,,D002771,001.9,A00,10008631,
mondo:0015767,trisomy 4p,"['trisomy of the short arm of chromosome 4', 'trisomy type 4p', 'chromosome 4p duplication', 'Duplication 4p', 'partial trisomy 4p', 'Duplication of the short arm of chromosome 4', '4p duplication', '4p trisomy']",,,1738,,,,,C537643,,,,
mondo:0015768,trisomy 5p,"['5p trisomy', 'Duplication of the short arm of chromosome 5', 'trisomy of the short arm of chromosome 5', 'partial trisomy 5p', 'Duplication 5p', '5p duplication', 'trisomy type 5p', 'chromosome 5p duplication']",,,1742,,,,,,,,,
mondo:0015769,distal trisomy 6p,"['telomeric duplication 6p', 'distal duplication 6p', 'trisomy 6pter', 'distal trisomy type 6p']",,,1745,C4302551,,,,,,,,
mondo:0015770,congenital hypogonadotropic hypogonadism,,,,174590,C3899503,,C120162,,,,E23.0,,
mondo:0015771,mosaic trisomy 7,"['Mosaic trisomy chromosome 7', 'Mosaic trisomy type 7', 'trisomy 7 mosaicism']",,,1747,CN036006,,,,C537822,,,,
mondo:0015772,trisomy 8q,"['partial trisomy 8q', 'chromosome 8q duplication', 'Duplication 8q', '8q duplication', '8q trisomy', 'trisomy type 8q']",,,1752,C0795829,,C36428,,C538020,,,,
mondo:0015773,fibular dimelia-diplopodia syndrome,['leg duplication-mirror foot syndrome'],,,1757,CN200350,,,,,,,,
mondo:0015774,thoraco-abdominal enteric duplication,['thoraco abdominal enteric duplication'],,,1759,,,,,,,,,
mondo:0015775,non-rhizomelic chondrodysplasia punctata,,,,176,,,,,,,,,
mondo:0015776,rhizomelic chondrodysplasia punctata,"['chondrodysplasia punctata, rhizomelic form', 'RCDP', 'rhizomelic chondrodysplasia punctata syndrome', 'rhizomelic dwarfism']",2580,,177,C0282529,"['-0.3713', '0.3562', '0.5215', '-0.7754', '0.626', '-0.2722', '-0.219', '1.38', '-0.3872', '-0.5405', '-0.125', '0.03062', '0.2588', '0.267', '0.0748', '-0.429', '0.5273', '-0.0861', '-0.3975', '-0.6626', '-0.1246', '-0.3022', '0.5264', '-0.1866', '-0.1665', '-0.04852', '-0.10016', '-0.343', '-0.05817', '-0.05197', '-0.2084', '-0.574', '-0.09174', '0.4082', '-0.2651', '0.6333', '0.3906', '-0.2534', '-0.3923', '0.2747', '0.0699', '-0.4153', '-0.1232', '0.3623', '0.02437', '-0.3413', '-0.3247', '-0.4778', '0.483', '0.622', '-0.1239', '-0.4612', '0.3845', '-0.722', '-0.641', '-0.4426', '-0.00979', '-0.06995', '0.47', '0.02454', '0.6797', '-0.303', '0.1418', '0.04874', '0.0791', '-0.2483', '0.5825', '-0.05658', '-0.013115', '0.10394', '-0.1578', '0.5024', '-0.08', '-0.3323', '0.709', '0.1986', '0.4214', '-0.2104', '-0.3923', '-0.3142', '-0.6807', '-0.10004', '0.03091', '0.845', '-0.3684', '0.4626', '-0.1026', '0.001048', '0.1578', '0.263', '0.014534', '0.07477', '-0.003466', '0.465', '0.07806', '0.3708', '0.6313', '0.0557', '0.3975', '-0.651']",C85047,,D018902,,E71.540,,
mondo:0015777,adult hypothyroidism,['rare adult hypothyroidism'],,,177101,CN226738,,,,,,,,
mondo:0015778,syndromic hypothyroidism,"['syndrome associated with hypothyroidism', 'syndromic hypothyroidism']",,,177107,CN226739,,,,,,,,
mondo:0015779,"45,X/46,XY mixed gonadal dysgenesis","['45,X/46,XY gonadal dysgenesis', 'Mixed gonadal dysgenesis', '45,X/46,XY MGD', '45,X0/46,XY MGD', '45,X0/46,XY mixed gonadal dysgenesis', '45,X/46,XY disorder of Sex development']",0080656,,1772,C0018055,,C120199,,,,,,
mondo:0015780,dyskeratosis congenita,"['MONDO:DC', 'DKC', 'Zinsser Cole Engman syndrome', 'Zinsser-Engman-Cole syndrome', 'Hoyeraal-Hreidarsson syndrome']",2729,,1775,C0265965,"['0.2188', '-0.1315', '-0.1844', '-0.8423', '0.1398', '-0.0619', '0.351', '1.099', '-0.51', '-0.635', '0.3613', '-0.5273', '-0.3708', '-0.1885', '-0.10486', '0.035', '0.731', '-0.3557', '-0.2489', '-0.8926', '-0.4824', '-0.2715', '0.4116', '-0.6587', '0.4402', '0.6943', '0.4097', '0.3408', '-0.4534', '-0.5566', '0.5376', '-0.0661', '0.2043', '0.1914', '0.7812', '0.507', '-0.2124', '-0.351', '0.0066', '-0.185', '-0.4963', '0.169', '0.5186', '-0.639', '-0.173', '-0.3828', '-0.2273', '0.2903', '0.1578', '-0.502', '0.0635', '0.4863', '0.3708', '0.08203', '-0.4814', '-0.3364', '-0.0816', '0.145', '-0.504', '-0.5176', '0.006268', '0.05228', '-0.2452', '0.0983', '0.03125', '0.4417', '0.4766', '0.4685', '-0.09607', '0.834', '-0.10284', '-0.1672', '-0.1879', '0.928', '0.4807', '-0.4282', '-0.1192', '-0.704', '0.323', '-0.6616', '-0.259', '0.2964', '-0.5073', '0.04578', '-0.5435', '0.3977', '0.3347', '0.3164', '0.4211', '0.02554', '0.1401', '-0.3826', '-0.0264', '0.1621', '0.3782', '-0.09753', '0.215', '0.09784', '0.0291', '-0.2195']",C111802,,D019871,,,10062759,
mondo:0015781,facial dysmorphism-shawl scrotum-joint laxity syndrome,"['Seaver-Cassidy syndrome', 'facial dysmorphism shawl scrotum joint laxity', 'Seaver Cassidy syndrome', 'hypertelorism, downslanting palpebral fissures, malar hypoplasia, and apparently low-set ears associated with joint and scrotal anomalies']",,,1778,C2931522,,,,C537529,,,,
mondo:0015782,dysmorphism-cleft palate-loose skin syndrome,,,,1779,CN200364,,,,,,,,
mondo:0015783,Prader-Willi syndrome due to paternal deletion of 15q11q13 type 1,['Prader-Willi syndrome (Type 1)'],,,177901,CN200365,,,,,,,,
mondo:0015784,Prader-Willi syndrome due to paternal deletion of 15q11q13 type 2,['Prader-Willi Syndrome (Type 2)'],,,177904,CN200366,,,,,,,,
mondo:0015785,Prader-Willi syndrome due to translocation,,,,177907,CN200367,,,,,,,,
mondo:0015786,Prader-Willi syndrome due to imprinting mutation,,,,177910,CN200368,,,,,,,,
mondo:0015787,symptomatic form of hemophilia A in female carriers,,,,177926,CN200369,,,,,,,,
mondo:0015788,symptomatic form of hemophilia B in female carriers,,,,177929,CN200370,,,,,,,,
mondo:0015790,central diabetes insipidus,"['diabetes insipidus neurogenic', 'neurogenic diabetes insipidus', 'diabetes insipidus cranial type', 'diabetes insipidus neurohypophyseal', 'CDI']",0081055,,178029,,,,,,,E23.2,10068587,0000863
mondo:0015791,peripheral precocious puberty,"['precocious pseudopuberty', 'gonadotropin independent precocious puberty', 'gonadotropin-independent precocious puberty', 'GIPP']",,,178040,,,,,,,,,
mondo:0015792,transient congenital hypothyroidism,"['hypothyroxinemia of prematurity', 'transient hypothyroxinemia of prematurity', 'THOP']",,,178045,C3827793,,C113171,,,,,,
mondo:0015793,moderate multiminicore disease with hand involvement,,,,178145,C1861753,,,,,,,,
mondo:0015794,antenatal multiminicore disease with arthrogryposis multiplex congenita,"['multiminicore myopathy, antenatal onset, with arthrogryposis', 'multicore myopathy, antenatal onset, with arthrogryposis']",,,178148,C1843691,,,,,,,,
mondo:0015795,undifferentiated embryonal sarcoma of the liver,"['embryonal sarcoma of the liver', 'undifferentiated sarcoma of the liver', 'UES']",,,178315,,,,,,,,,
mondo:0015796,acute lung injury,,,,178320,,,C155766,0004610,D055371,,,10069351,
mondo:0015797,UV-sensitive syndrome,"['UV sensitive syndrome', 'UVSS']",0060240,,178338,,"['0.4548', '0.2896', '-0.6733', '-0.3171', '0.158', '-0.3276', '-0.02542', '-0.1628', '0.02843', '-0.1764', '0.561', '0.4836', '-0.1349', '-0.00775', '-0.1227', '-0.01226', '0.4773', '0.02237', '-0.2009', '-0.2069', '-0.4236', '-0.4424', '-0.0385', '-0.1475', '0.2512', '0.3564', '-0.528', '0.3071', '0.1047', '-0.3584', '0.583', '-0.612', '0.244', '0.06995', '0.06152', '0.3574', '0.0757', '-0.3157', '0.03162', '-0.4443', '0.05258', '-0.656', '-0.05276', '-0.545', '-0.2394', '-0.3977', '0.1953', '0.04315', '0.1388', '-0.1776', '0.09973', '-0.1192', '0.0612', '0.3035', '-0.3125', '0.2512', '0.0662', '0.1384', '-0.2493', '-0.3853', '0.09344', '-0.1975', '-0.19', '-0.02492', '-0.0172', '0.424', '0.1984', '0.5347', '0.05835', '0.9673', '-0.2747', '0.2092', '0.3645', '0.032', '0.3918', '0.06995', '-0.074', '0.0987', '0.02823', '0.0903', '-0.2764', '-0.1938', '0.5137', '-0.01101', '-0.0592', '-0.584', '0.0305', '0.2117', '0.4946', '0.1255', '0.0832', '0.3232', '-0.252', '0.12115', '0.4768', '0.3813', '0.3457', '-0.2363', '-0.06094', '-0.0821']",,,C563466,702.8,,,
mondo:0015798,inflammatory myofibroblastic tumor,"['inflammatory fibrosarcoma', 'inflammatory myofibroblastic tumor', 'IMT', 'inflammatory pseudotumor', 'inflammatory myofibroblastic neoplasm']",0050905,,178342,C0334121,,C6481,,D006104,,,10067917,
mondo:0015799,Smith-McCort dysplasia,"['Smith-McCort dwarfism', 'Smith McCort dysplasia']",0060247,,178355,,"['-0.667', '0.3586', '0.3367', '-0.4038', '0.05597', '-0.4424', '0.233', '0.0664', '-0.6724', '-0.6694', '-0.3872', '0.136', '-0.1211', '0.5103', '0.2583', '0.2954', '0.5957', '-0.3188', '-0.2556', '-1.021', '-0.01007', '0.4314', '1.506', '0.0867', '-0.09985', '0.2103', '-0.04315', '-0.274', '0.2776', '0.2607', '0.4346', '-0.002571', '-0.1979', '0.4346', '0.2766', '0.02156', '-0.3984', '0.0612', '-0.1765', '-0.0852', '0.1611', '-0.8013', '0.01955', '0.1293', '0.1377', '-0.5103', '0.03284', '0.6196', '0.3025', '-0.1802', '0.3538', '0.1349', '-0.2869', '0.02835', '-0.4548', '-0.958', '-0.142', '-0.4016', '-0.06494', '0.1531', '0.02248', '0.0745', '-0.6523', '-0.0487', '0.236', '0.1248', '0.579', '0.03967', '-0.184', '-0.0797', '-0.5264', '-0.3489', '0.1912', '-0.4724', '-0.1953', '0.3723', '-0.4067', '-0.503', '-0.2383', '-0.7217', '0.06665', '0.5615', '-0.3718', '0.0567', '-0.2908', '0.07526', '-0.085', '0.0873', '0.8833', '0.32', '-0.03543', '0.3909', '-0.2756', '0.2634', '0.4639', '0.3154', '0.10095', '-0.1862', '0.4265', '0.2383']",,,C564589,,,,
mondo:0015800,osteosclerosis-developmental delay-craniosynostosis syndrome,,,,178377,CN200391,,,,,,,,
mondo:0015801,hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation,,,,178396,CN200394,,,,,,,,
mondo:0015802,autosomal dominant non-syndromic intellectual disability,"['autosomal dominant non-syndromic intellectual disability', 'non-syndromic intellectual disability, autosomal dominant', 'autosomal dominant non-syndromic mental retardation', 'autosomal dominant mental retardation']",0060307,,178469,CN200399,"['-0.09436', '0.0935', '0.1324', '-0.1622', '0.1271', '-0.2815', '-0.007004', '0.235', '-0.12164', '-0.2389', '-0.0968', '-0.0677', '-0.0109', '-0.04733', '0.1318', '-0.01181', '0.01364', '-0.0647', '-0.08105', '-0.425', '-0.0754', '0.0872', '0.0824', '-0.05984', '0.1656', '0.03806', '-0.0794', '-0.11664', '0.0532', '-0.2064', '0.1371', '0.04016', '0.2412', '0.1493', '-0.03818', '-0.1318', '-0.0836', '-0.2373', '-0.000227', '-0.2026', '0.139', '-0.2544', '0.07404', '-0.02023', '-0.07776', '-0.3096', '-0.10657', '0.072', '0.03732', '-0.02014', '0.02994', '0.0063', '-0.014435', '-0.1715', '-0.05344', '-0.11884', '0.181', '0.02495', '-0.2074', '0.10077', '0.1206', '-0.03445', '0.1005', '0.04736', '0.012', '0.03026', '0.0466', '0.1705', '-0.1791', '0.1598', '-0.2157', '-0.05847', '0.05212', '-0.1881', '0.1553', '0.1266', '0.0628', '-0.01246', '-0.155', '-0.012024', '-0.05438', '0.032', '-0.04913', '0.265', '0.1277', '0.05423', '0.05676', '0.224', '0.09656', '0.1995', '0.07574', '0.2944', '0.007236', '0.004604', '0.491', '0.1097', '0.2957', '-0.2832', '0.09814', '0.1652']",,,,,,,
mondo:0015803,wound botulism,"['inoculation botulism', 'cutaneous toxin-mediated botulism', 'skin infectious botulism', 'cutaneous infectious botulism', 'skin toxin-mediated botulism']",0050353,,178475,C1306794,,C128342,,,040.42,A48.52,,
mondo:0015804,infant botulism,"['infantile botulism', 'infant intestinal toxin-mediated botulism', 'infant intestinal botulism', 'botulism of infancy', 'infantile onset botulism', 'infant intestinal toxaemia botulism', 'infant intestinal toxemia botulism']",0050354,,178478,C0238027,,C128343,,,,A48.51,,
mondo:0015805,intestinal botulism,"['intestinal toxaemia botulism', 'intestinal toxin-mediated botulism', 'intestinal colonisation botulism', 'intestinal colonization botulism', 'intestinal toxemia botulism']",0050141,,178481,C1443901,,,,,,,,
mondo:0015806,adult intestinal botulism,"['adult intestinal toxemia botulism', 'adult intestinal toxin-mediated botulism', 'adult intestinal colonization botulism', 'adult intestinal toxaemia botulism', 'intestinal botulism of adults', 'adult intestinal colonisation botulism', 'infant-like botulism']",,,178487,C4289991,,C128344,,,,,,
mondo:0015807,myopic macular degeneration,['myopic maculopathy'],,,178493,C0730271,,,0009201,,,H35.3,,
mondo:0015808,folliculotropic mycosis fungoides,"['mycosis fungoides-associated follicular mucinosis', 'follicular mycosis fungoides']",,,178512,C1627767,,C35685,,,701.8,,,
mondo:0015809,localized pagetoid reticulosis,"['localised reticulosis', 'pagetoid reticulosis', 'pagetoid reticulosis, Woringer-Kolopp type']",,,178517,C1276140,,C35794,,D056267,202.70,C84.0,,
mondo:0015810,primary cutaneous CD4+ small/medium-sized pleomorphic T-cell lymphoma,,,,178522,,,,,,,C84.4,,
mondo:0015811,primary cutaneous aggressive epidermotropic CD8+ T-cell lymphoma,"['Berti lymphoma', 'primary cutaneous epidermotropic cytotoxic CD8+ T-cell lymphoma']",,,178528,,,,,,,C84.4,,
mondo:0015812,primary cutaneous gamma/delta-positive T-cell lymphoma,,,,178533,,,,,,,C84.4,,
mondo:0015813,primary cutaneous marginal zone B-cell lymphoma,"['marginal zone B cell lymphoma of the skin', 'salt lymphoma', 'cutaneous Immunocytoma', 'skin-associated lymphoid tissue lymphoma', 'marginal zone B cell lymphoma of skin', 'Primary cutaneous marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue', 'Primary cutaneous marginal zone lymphoma of mucosa-associated lymphoid tissue', 'PCMZL', 'Primary cutaneous marginal zone B cell lymphoma of mucosa-associated lymphoid tissue', 'C-MALT']",,,178536,C1275321,,C7230,,,,,,
mondo:0015814,primary cutaneous follicle center lymphoma,"['cutaneous follicle centre lymphoma', 'cutaneous follicle center lymphoma', 'Reticulohistiocytoma of the dorsum', 'Crosti^s disease', 'PCFCL']",,,178540,C1333171,,C7217,,,,,,
mondo:0015816,indolent primary cutaneous T-cell lymphoma,,,,178548,,,,,,,,,
mondo:0015817,aggressive primary cutaneous T-cell lymphoma,,,,178551,,,,,,,,,
mondo:0015818,aggressive primary cutaneous B-cell lymphoma,,,,178554,,,,,,,,,
mondo:0015819,indolent primary cutaneous B-cell lymphoma,,,,178557,,,,,,,,,
mondo:0015820,primary cutaneous B-cell lymphoma,,,,178563,C1274310,,,,,202.80,,,
mondo:0015821,mycosis fungoides and variants,,,,178566,CN226743,,,,,,,,
mondo:0015822,acquired neutropenia,"['immunologic neutropenia', 'acquired neutropenia']",,,178996,,,,,,,,,
mondo:0015823,primary immunodeficiency due to a defect in adaptive immunity,,,,179006,,,,,,,,,
mondo:0015824,oculomaxillofacial dysostosis,"['oculomaxillofacial dysplasia with oblique facial clefts', 'Richieri Costa Gorlin syndrome', 'oblique facial clefts', 'Richieri-Costa-Gorlin syndrome']",,,1794,C1838348,,,,C537736,,,,
mondo:0015826,autosomal dominant spondylocostal dysostosis,"['spondylocostal dysostosis, autosomal dominant', 'autosomal dominant spondylocostal dysplasia']",,,1797,CN200437,,,,,,,,
mondo:0015827,distal renal tubular acidosis,"['distal renal tubular acidosis (disease)', 'renal tubular acidosis type 1', 'familial distal primary acidosis', 'distal renal tubular acidosis', 'renal tubular acidosis, distal', 'classic RTA', 'dRTA']",,,18,,"['-0.176', '-0.3748', '-0.6763', '-0.3984', '-0.1124', '-0.2573', '-0.6104', '1.081', '-0.0766', '0.223', '-0.6567', '-0.2485', '-0.4912', '0.7446', '-0.1367', '-0.3103', '-0.3567', '-0.1404', '-0.1616', '-0.675', '-0.1742', '-0.983', '0.784', '0.5796', '0.776', '0.03235', '-0.722', '-0.2318', '-0.1709', '-0.4502', '-0.02766', '-0.5864', '0.2727', '-0.0498', '-0.3828', '-0.381', '-0.419', '0.0984', '-0.04547', '-0.2708', '-0.3154', '-0.544', '0.579', '-0.2343', '-0.1004', '-0.634', '-0.3193', '-0.1559', '-0.0859', '0.2388', '0.2666', '-0.265', '0.1771', '-0.7236', '-0.1864', '-0.2465', '0.4521', '-0.02617', '-0.3833', '0.5283', '-0.0908', '-0.1804', '-0.02864', '-0.5503', '-0.1672', '0.09515', '-0.1989', '0.321', '-0.1593', '0.08405', '-0.01949', '-0.06696', '0.4958', '0.09875', '0.6523', '0.1516', '0.1681', '-0.594', '-0.04913', '-0.0886', '-0.2125', '0.01663', '0.3672', '0.1333', '-0.07513', '0.4128', '0.1956', '-0.513', '0.3462', '0.4841', '0.3804', '-0.1466', '0.1748', '-0.6343', '0.378', '0.296', '1.008', '-0.5044', '-0.75', '0.0531']",,,,588.89,,10045224,0008341
mondo:0015828,uterovaginal malformation,,,,180062,,,,,,,,,
mondo:0015829,non-syndromic uterovaginal malformation,"['isolated uterovaginal malformation', 'nonsyndromic uterovaginal malformation']",,,180065,,,,,,,,,
mondo:0015830,partial bilateral aplasia of the mullerian ducts,"['incomplete bilateral aplasia of the Mullerian ducts', 'incomplete bilateral aplasia of the Müllerian ducts', 'partial bilateral aplasia of the Müllerian ducts']",,,180068,,,,,,,,,
mondo:0015831,unilateral aplasia of the mullerian ducts,"['unilateral aplasia of the Müllerian ducts', 'unicornuate uterus']",,,180071,,,,,,,,,
mondo:0015832,true unicornuate uterus,"['complete unilateral aplasia of the Mullerian ducts', 'complete unilateral aplasia of the Müllerian ducts', 'complete unilateral Müllerian aplasia', 'unicornuate uterus without rudimentary horn', 'complete unilateral Mullerian aplasia']",,,180074,,,,,,,,,
mondo:0015833,pseudounicornuate uterus,"['incomplete unilateral Müllerian aplasia', 'incomplete unilateral aplasia of the Müllerian ducts', 'incomplete unilateral aplasia of the Mullerian ducts', 'unicornuate uterus with rudimentary horn', 'incomplete unilateral Mullerian aplasia']",,,180079,,,,,,,,,
mondo:0015834,didelphys uterus,['Bicervical bicornuate uterus'],,,180086,,,,,,752.2,,10012770,
mondo:0015835,Bicervical bicornuate uterus and blind hemivagina,,,,180106,,,,,,,,,
mondo:0015836,Bicervical bicornuate uterus with patent cervix and vagina,,,,180111,,,,,,,,,
mondo:0015837,Unicervical bicornuate uterus,,,,180114,,,,,,,,,
mondo:0015838,cordiform uterus,"['uterus arcuatus', 'uterus cordiformis']",,,180118,,,,,,,,,
mondo:0015839,septate uterus,,,,180122,,,,,,,,10062606,
mondo:0015840,complete septate uterus,['total septate uterus'],,,180126,,,,,,,,,
mondo:0015841,partial septate uterus,"['subtotal septate uterus', 'uterus subseptus']",,,180129,,,,,,,,,
mondo:0015842,bicornuate uterus,,,,180134,,,,,,,,10004550,
mondo:0015843,uterine hypoplasia,,,,180139,,,,,,,,10063146,
mondo:0015844,agenesis and aplasia of uterine body,,,,180142,,,,,,,,,
mondo:0015845,uterine cervical aplasia and agenesis,,,,180145,,,,,,,,,
mondo:0015846,syndromic uterovaginal malformation,"['syndrome associated with uterovaginal malformation', 'syndromic uterovaginal malformation']",,,180148,CN226751,,,,,,,,
mondo:0015849,longitudinal vaginal septum,,,,180157,,,,,,,,,0008740
mondo:0015850,transverse vaginal septum,,,,180160,,,,,,,Q52.11,,0000145
mondo:0015852,excess breast volume or number,,,,180170,,,,,,,,,
mondo:0015853,deficient breast volume or number,,,,180173,,,,,,,,,
mondo:0015854,supernumerary breasts,"['accessory breasts', 'polymastia']",,,180182,,,,,,,,10049786,
mondo:0015855,isolated congenital breast hypoplasia/aplasia,"['breasts and/or nipples, aplasia or hypoplasia of', 'isolated congenital amastia']",,,180188,,,,,,,,,
mondo:0015856,syndromic breast hypoplasia/aplasia,,,,180193,CN226755,,,,,,,,
mondo:0015860,anomaly of puberty or/and menstrual cycle,,,,180208,,,,,,,,,
mondo:0015863,polyembryoma,['gonadal polyembryoma'],,,180229,C0334518,,C66776,,,,,,
mondo:0015864,mixed germ cell tumor,"['combined germ cell tumour', 'combined germ cell neoplasm', 'mixed germ cell cancer', 'mixed germ cell tumor', 'mixed germ cell neoplasm', 'combined germ cell tumor']",3306,,180234,C0334524,,C4290,,,,,,
mondo:0015867,vaginal carcinoma,"['cancer of the vagina', 'vaginal malignant epithelial tumor', 'vaginal cancer', 'vagina cancer', 'cancer of vagina', 'vagina carcinoma', 'vaginal malignant epithelial tumour', 'carcinoma of vagina', 'carcinoma of the vagina', 'vaginal carcinoma', 'vaginal cancer, NOS']",0050918,,180247,C0262659,,C3917,,,,,,
mondo:0015871,benign breast phyllodes tumor,"['cystosarcoma phyllodes', 'phyllodes tumor, benign (morphologic abnormality)', 'BPT', 'benign breast phyllodes tumor', 'benign phyllodes tumor of the breast', 'benign phyllodes tumor of breast', 'phyllode tumour of the breast', 'phyllodes neoplasm', 'benign cystosarcoma phyllodes', 'cystosarcoma phyllode of the breast', 'benign phyllodes neoplasm of breast', 'phylloide tumour of the breast', 'cystosarcoma phyllode', 'phylloide tumor of the breast', 'cystosarcoma phylloide of the breast', 'phyllode tumor of the breast', 'cystosarcoma phyllodes NOS (morphologic abnormality)', 'benign phyllodes neoplasm of the breast', 'benign phyllodes tumour of the breast', 'benign phyllodes tumour of breast', 'benign phyllodes neoplasm', 'cystosarcoma phylloide', 'breast phyllodes tumor, benign', 'breast benign phyllodes neoplasm']",1631,,180261,C1332533,,C5196,,,,,10011813,
mondo:0015872,giant adenofibroma of the breast,,,,180267,CN200476,,,,,,,,
mondo:0015873,Paget disease of the nipple,"['PD', 'nipple Paget^s disease', 'Paget^s disease, mammary', 'Paget disease of the breast', 'mammary Paget disease', 'Paget^s disease of the nipple', 'Paget^s disease of nipple', 'Paget disease of the nipple']",,,180275,C1704323,,C3301,,,,,10033367,
mondo:0015874,benign ductal tumor of breast,,,,180284,CN200479,,,,,,,,
mondo:0015883,"hidrotic ectodermal dysplasia, Halal type","['Halal-Setton-Wang syndrome', 'hidrotic ectodermal dysplasia Halal type', 'ectodermal dysplasia with skin anomalies and intellectual disability', 'Halal Setton Wang syndrome', 'trichodysplasia-abnormal dermatoglyphics-intellectual disability syndrome']",,,1809,C2930953,,,,C535621,,,,
mondo:0015884,autosomal dominant hypohidrotic ectodermal dysplasia,"['hypohidrotic ectodermal dysplasia, autosomal dominant', 'autosomal dominant anhidrotic ectodermal dysplasia', 'AD-HED']",,,1810,,"['-0.04004', '0.1855', '0.1993', '-0.1534', '0.2263', '-0.2333', '-0.0419', '0.1897', '-0.01101', '-0.2952', '-0.0868', '-0.05887', '-0.1202', '-0.0396', '0.0747', '0.04605', '0.01926', '-0.06744', '-0.1302', '-0.3887', '-0.1395', '0.01351', '0.193', '-0.10156', '0.02882', '0.10803', '-0.2013', '-0.1373', '0.1539', '-0.287', '0.09644', '0.131', '0.1074', '0.0604', '0.0689', '-0.1152', '-0.02339', '-0.2603', '0.02875', '-0.3252', '0.03217', '-0.2042', '0.02408', '-0.1772', '-0.1709', '-0.2957', '-0.1317', '0.1371', '0.1569', '-0.1531', '0.2062', '-0.0456', '0.09503', '0.01322', '-0.095', '-0.2803', '0.1958', '-0.0916', '-0.3167', '-0.01839', '0.2424', '0.08624', '-0.08344', '-0.02264', '0.05148', '-0.0474', '0.2256', '0.05542', '-0.1702', '0.1973', '-0.2656', '-0.1729', '0.0263', '-0.1262', '0.1147', '0.0489', '-0.0709', '0.001308', '-0.1109', '-0.1114', '0.00802', '0.1733', '0.02373', '0.281', '-0.0644', '0.09204', '0.1406', '0.286', '0.1364', '0.1901', '0.03632', '0.1177', '0.01409', '0.1036', '0.5176', '0.1092', '0.3186', '-0.3333', '-0.0283', '0.1967']",,,,,,,
mondo:0015892,growth hormone insensitivity syndrome,"['GHIS', 'short stature due to a defect in growth hormone receptor or post-receptor pathway', 'Growth hormone insensitivity syndromes']",,,181393,CN200504,,C129867,,,,,,
mondo:0015898,adrenogenital syndrome,['congenital adrenal hyperplasia'],,,181412,CN200506,,,,D047808,255.2,,10061630,
mondo:0015900,hypoaldosteronism disease,"['hypoaldosteronism', 'rare hypoaldosteronism']",,,181419,C0020595,,,,D006994,,,,
mondo:0015902,major hypertriglyceridemia,,,,181425,,,,,,,,,
mondo:0015903,hyperalphalipoproteinemia,['HALP1'],,,181428,C0342883,,C128806,,,272.4,,,
mondo:0015905,syndromic dyslipidemia,"['rare syndromic dyslipidaemia', 'syndromic inherited lipid metabolism disorder', 'syndrome associated with inherited lipid metabolism disorder', 'rare syndromic dyslipidemia', 'complex dyslipidaemia']",,,181437,C3875286,,,,,,,,
mondo:0015907,epimetaphyseal skeletal dysplasia,,,,1819,,,,,,,,,
mondo:0015908,chromomycosis,"['chromoblastomycosis', 'chromomycosis', 'Chromomycoses', 'Chromoblastomycoses', 'mossy foot disease', 'dermatitis Verrucosa', 'Chromomycosis']",1562,,182,C3245522,,,0007207,D002862,117.2,,10008803,
mondo:0015909,aplastic anemia,,12449,,182040,,,C2870,,D000741,284.9,,,
mondo:0015912,macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss,"['May-Hegglin anomaly', 'MYH9-related disorder', 'MYH9-RD', 'Fechtner syndrome', 'MYH9 related thrombocytopenia', 'MHA', 'MYH9-related syndromic thrombocytopenia', 'macrothrombocytopenia and granulocyte inclusions with or without nephritis or sensorineural hearing loss', 'Brodie Chole griffin syndrome', 'macrothrombocytopenia, nephritis, and deafness', 'May-Hegglin thrombocytopenia', 'MYH9-related syndrome', 'Epstein syndrome', 'Brodie Chole gryphon syndrome', 'Dohle leukocyte inclusions with giant platelets', 'matins', 'SBS', 'MYH9 related disorders', 'macrothrombocytopenia progressive deafness', 'macrothrombocytopenia and progressive sensorineural deafness', 'FTNS', 'Alport syndrome with macrothrombocytopenia, formerly', 'Alport syndrome with macrothrombocytopenia', 'MYH9-related disease', 'macrothrombocytopenia with leukocyte inclusions', 'bleeding disorder, Platelet-type, 6', 'giant platelet syndrome with thrombocytopenia', 'macrothrombocytopenia, nephritis, deafness, and leukocyte inclusions', 'Sebastian syndrome', 'MYH-9 related disease', 'macrothrombocytopenia with dispersed leukocytic inclusions', 'Sebastian platelet syndrome']",0060651,605249,850,CN226270,"['-0.2278', '-0.3499', '-0.4233', '0.1653', '0.1571', '0.193', '-0.3716', '1.106', '0.1619', '-0.03503', '-0.07654', '-0.0776', '0.2312', '0.608', '0.2847', '-0.648', '-0.423', '0.169', '0.6025', '-0.2012', '-0.03162', '0.03986', '0.5073', '-0.1855', '0.072', '-0.523', '-0.4636', '0.1306', '0.2644', '0.1493', '0.508', '-0.282', '0.06223', '0.5654', '-0.003796', '-0.892', '-0.395', '-0.3484', '0.3142', '-0.1488', '-0.06665', '-0.1715', '0.68', '-0.2598', '0.01267', '-0.3037', '-0.622', '-0.3818', '-0.094', '0.3018', '0.2109', '0.764', '-0.03693', '-0.1605', '0.07666', '-0.2014', '0.732', '-0.324', '-0.7705', '0.005867', '-0.0735', '-0.504', '0.374', '-0.4873', '-0.307', '-0.157', '0.443', '0.09064', '-0.1335', '0.3718', '-0.1538', '0.05496', '0.113', '-0.10565', '1.096', '-0.4485', '0.711', '-0.2866', '0.2062', '0.1559', '-0.519', '0.2272', '-0.10657', '0.5513', '-0.4304', '0.02946', '0.355', '0.4204', '-0.1982', '-0.3794', '0.9365', '1.086', '-0.02791', '-0.156', '0.6084', '0.076', '0.2717', '-0.622', '-0.01834', '-0.07025']",C158788,,C537831,759.89,,,
mondo:0015914,primary orthostatic hypotension,['neurogenic orthostatic hypotension'],,,448426,,,,,,,,,
mondo:0015915,cerebellar malformation,,,,182061,,,,,,,,,
mondo:0015921,ARX-related epileptic encephalopathy,,,,182079,,,,,,,,,
mondo:0015923,acquired peripheral neuropathy,['acquired peripheral neuropathy'],,,182086,,,,,,,,,
mondo:0015924,pulmonary arterial hypertension,"['PAH with overt features of venous/capillaries involvement', 'PPH', 'PVOD/PCH', 'idiopathic pulmonary hypertension', 'PAH']",,,182090,CN200519,,,,D000081029,,,10064911,
mondo:0015925,interstitial lung disease,"['interstitial lung disease', 'ILD']",3082,,182095,C0206062,"['0.4192', '-0.3762', '-0.614', '0.1907', '0.001727', '-0.2188', '0.954', '-0.1628', '-0.5513', '-0.1849', '0.3347', '0.10516', '-1.107', '0.264', '-0.14', '-0.4846', '-0.2255', '0.4336', '0.2458', '-0.652', '0.3418', '-0.5635', '0.6', '-0.4595', '0.2289', '-0.1214', '0.06235', '0.751', '0.1266', '0.2844', '0.579', '0.11456', '1.003', '-0.1788', '0.4753', '0.05164', '-0.3276', '-0.0502', '0.3828', '-0.02058', '-0.1131', '-0.1887', '-0.469', '0.09955', '0.446', '-0.0334', '-0.0751', '0.028', '0.2498', '0.1254', '-0.1766', '-0.0664', '0.5273', '-0.02899', '-0.1707', '-0.1669', '-0.602', '0.696', '-0.72', '-0.069', '-0.1967', '0.801', '-0.1569', '0.0695', '-0.492', '-0.292', '0.665', '0.5396', '-0.9814', '0.6943', '-0.8237', '0.2163', '1.013', '0.1951', '-0.08154', '0.456', '0.12134', '-0.00248', '-0.3684', '-0.536', '-0.3687', '0.0628', '-0.1194', '0.10095', '-0.1247', '0.2756', '0.2588', '0.1589', '0.1718', '-0.2224', '0.6343', '-0.261', '-0.865', '0.3381', '0.3975', '0.4753', '-0.2123', '-0.1742', '-0.59', '-0.07886']",C164315,0004244,D017563,,J80-J84,10022611,
mondo:0015926,pneumoconiosis,"['Black lung disease', 'coal worker^s pneumoconiosis']",10316,,182098,C0032273,,C26861,,D011009,505,,10035653,
mondo:0015927,idiopathic eosinophilic pneumonia,,,,182101,C3872845,,,,,,,,
mondo:0015929,thoracic malformation,,,,182108,,,,,,,,,
mondo:0015930,respiratory malformation,,,,182111,,,,,,,,,
mondo:0015932,non-syndromic urogenital tract malformation of female,"['nonsyndromic urogenital tract malformation of female', 'female organism non-syndromic urogenital tract malformation', 'non-syndromic urogenital tract malformation of female organism', 'isolated urogenital tract malformation of female']",,,182117,,,,,,,,,
mondo:0015933,non-syndromic urogenital tract malformation of male,"['isolated urogenital tract malformation of male', 'non-syndromic urogenital tract malformation of male organism', 'male organism non-syndromic urogenital tract malformation', 'nonsyndromic urogenital tract malformation of male']",,,182121,,,,,,,,,
mondo:0015935,extragonadal germinoma,,,,182127,C0206660,,,,D018237,,,10018207,
mondo:0015941,epiphyseal dysplasia-hearing loss-dysmorphism syndrome,"['epiphyseal dysplasia hearing loss dysmorphism', 'Finucane Kurtz Scott syndrome', 'Finucane-Kurtz-Scott syndrome']",,,1825,CN200532,,,,,,,,
mondo:0015942,frontometaphyseal dysplasia,"['frontometaphyseal dysplasia', 'FMD']",0111785,,1826,,"['-0.526', '0.1181', '0.5645', '-0.531', '0.3328', '-0.6064', '0.604', '1.046', '-0.4797', '-0.4028', '-0.05157', '-0.3574', '-0.1838', '0.184', '-0.1338', '0.03937', '-0.01467', '-0.0591', '-0.4653', '-0.4773', '-0.1278', '0.1092', '0.5913', '0.01746', '0.56', '0.06305', '-0.10657', '0.1509', '0.3833', '0.0369', '0.02194', '-0.05515', '-0.06003', '0.359', '0.1942', '-0.6216', '0.1105', '-0.5503', '0.0931', '-0.07007', '-0.1608', '-0.2218', '0.01743', '-0.1272', '0.5796', '-0.0657', '0.1804', '0.81', '-0.251', '-0.0326', '-0.0778', '0.1382', '-0.05133', '-0.2062', '-0.594', '-0.768', '0.3118', '-0.1646', '0.001421', '-0.336', '-0.0153', '0.0404', '-0.476', '0.3347', '-0.5044', '-0.993', '0.2954', '0.6655', '-0.3857', '-0.10986', '-0.1906', '0.02924', '-0.11615', '0.158', '-0.2913', '0.3862', '0.4233', '0.2097', '-0.3145', '-0.459', '0.2009', '-0.129', '0.281', '0.5366', '0.02695', '0.3076', '-0.0519', '-0.013664', '-0.1649', '-0.1373', '-0.02193', '0.683', '0.7236', '0.4644', '0.8354', '-0.0855', '0.904', '-0.463', '0.1731', '0.1492']",,,C538064,759.89,,,
mondo:0015943,eosinophilic granulomatosis with polyangiitis,"['EGPA', 'allergic granulomatous and angiitis', 'allergic angiitides, granulomatous', 'vasculitis, Churg-Strauss', 'allergic angiitis and granulomatosis', 'allergic granulomatous angiitis', 'Churg Strauss syndrome', 'granulomatous allergic Angiitides', 'granulomatous allergic angiitis', 'granulomatous angiitis, allergic', 'angiitides, allergic granulomatous', 'Churg-Strauss syndrome', 'allergic granulomatous Angiitides', 'granulomatosis, allergic', 'vasculitides, eosinophilic granulomatous', 'allergic angiitides', 'granulomatous angiitides, allergic', 'vasculitis, Churg Strauss', 'syndrome, Churg-Strauss', 'angiitis, granulomatous allergic', 'allergic granulomatosis angiitis', 'granulomatoses, allergic', 'granulomatous vasculitides, eosinophilic', 'vasculitis, eosinophilic granulomatous', 'allergic angiitis, granulomatous', 'eosinophilic granulomatous vasculitis', 'allergic angiitis', 'Churg-Strauss vasculitis', 'angiitides, allergic', 'CSS', 'granulomatous vasculitis, eosinophilic', 'eosinophilic granulomatous Vasculitides', 'allergic granulomatosis', 'allergic granulomatoses', 'angiitis, allergic granulomatous', 'angiitis, allergic', 'angiitides, granulomatous allergic']",3049,,183,C0008728,,C34481,0007208,D015267,,,10048594,
mondo:0015944,axial mesodermal dysplasia spectrum,"['Russell Weaver Bull syndrome', 'blastogenesis defect', 'Russell-Weaver-Bull syndrome']",,,1834,C2931613,,,,C537790,,,,
mondo:0015947,inherited ichthyosis,"['inherited genetic ichthyosis', 'hereditary ichthyosis (disease)', 'genetic ichthyosis']",,,183435,,"['0.05792', '0.1423', '-0.0778', '0.1814', '0.2274', '-0.3271', '-0.0666', '-0.134', '-0.04745', '-0.2312', '0.1189', '0.2042', '0.0796', '-0.003029', '-0.1797', '-0.04117', '0.004787', '-0.1963', '-0.04605', '-0.585', '-0.1276', '0.01869', '0.3826', '0.0345', '0.02843', '-0.0986', '0.05457', '0.008224', '0.013855', '-0.0512', '0.2444', '0.1075', '0.0978', '0.1498', '-0.0877', '0.08215', '-0.0621', '0.08575', '0.0669', '-0.1528', '0.0806', '-0.2788', '0.1315', '0.0274', '-0.10785', '-0.0768', '-0.10486', '0.1672', '0.4146', '0.077', '-0.04645', '-0.2188', '-0.0422', '-0.11774', '-0.02246', '-0.3123', '0.2076', '0.1678', '-0.3691', '-0.05157', '0.2032', '0.011566', '0.1676', '0.1107', '-0.03008', '0.01682', '0.4265', '0.253', '-0.1934', '0.3232', '-0.287', '-0.1392', '0.1276', '0.0801', '0.04434', '0.106', '-0.03046', '0.0918', '-0.4534', '-0.1576', '0.05075', '0.0437', '-0.07574', '0.08624', '-0.2336', '-0.1273', '0.014854', '0.0519', '0.1685', '0.04987', '0.1499', '0.296', '0.11896', '0.1326', '0.1013', '0.1945', '0.2349', '-0.1432', '-0.03012', '-0.0516']",,,,757.1,Q80,10021202,
mondo:0015950,inherited skin tumor,"['genetic skin tumor', 'genetic skin tumour']",,,183487,CN200547,,,,,,,,
mondo:0015951,hereditary photodermatosis,"['photogénodermatose', 'genetic skin photosensitivity', 'photogenodermatosis']",,,183490,,,,,,,,,
mondo:0015961,hereditary head and neck malformation,['genetic head and neck malformation'],,,183583,,,,,,,,,
mondo:0015962,inherited renal tubular disease,['genetic renal tubular disease'],,,183592,CN200561,,,,,,,,
mondo:0015967,monogenic diabetes,,,,183625,,,C129739,,,,,,
mondo:0015974,severe combined immunodeficiency,"['combined T and B cell inborn immunodeficiency', 'SCID', 'severe combined immunodeficiency', 'severe combined immunodeficiency disease', 'severe combined immunodeficiency (disease)']",627,,183660,C0085110,"['-0.25', '0.578', '0.2224', '-0.1736', '0.487', '-0.04492', '0.727', '0.4739', '0.1107', '-0.4426', '-0.3987', '-0.3457', '-0.4822', '0.2242', '-0.3325', '-0.1544', '-0.11926', '-0.2283', '-0.4211', '-0.585', '-0.251', '-0.3022', '1.082', '-0.354', '-0.13', '0.2854', '-0.323', '0.09784', '-0.4302', '-0.559', '0.355', '1.121', '0.547', '-0.2018', '0.4382', '0.276', '-0.922', '-0.1372', '-0.3723', '0.00419', '-0.3157', '-0.2246', '-0.111', '-0.4692', '-0.4097', '-0.2996', '-0.02802', '-0.625', '-0.158', '0.7617', '0.3352', '-0.673', '0.1979', '-0.1787', '-0.1779', '0.634', '-0.2172', '-0.1873', '0.0707', '0.5234', '-0.1559', '0.4543', '0.02473', '0.4038', '0.481', '0.03967', '0.5825', '0.1769', '-0.4082', '0.5483', '-0.2113', '-0.266', '-0.442', '-0.5024', '0.605', '-0.1405', '0.475', '-0.3462', '0.1266', '0.05508', '0.1329', '-0.0874', '-0.0236', '0.06726', '0.04703', '-0.399', '0.3', '0.16', '-0.03168', '0.2947', '0.3997', '0.2632', '-0.1492', '0.4214', '0.37', '0.72', '-0.2275', '-0.5317', '-0.0117', '-0.176']",C3472,,D016511,,,10069566,0004430
mondo:0015975,hyper-IgM syndrome with susceptibility to opportunistic infections,['HIGM with susceptibility to opportunistic infections'],,,183663,CN200572,"['-0.362', '0.01091', '0.1742', '-0.531', '0.0215', '-0.081', '0.05176', '0.02051', '0.1026', '-0.0701', '-0.04437', '0.0955', '-0.1794', '0.0134', '-0.08826', '-0.1312', '0.1743', '0.2213', '-0.2286', '-0.5254', '0.00918', '-0.335', '0.6426', '0.05374', '0.1237', '0.01988', '0.05624', '-0.08813', '-0.1936', '-0.5435', '0.1388', '0.3206', '0.502', '0.3213', '0.2216', '-0.01567', '-0.5483', '0.07056', '-0.4353', '-0.5547', '-0.2751', '0.05322', '0.1637', '-0.3052', '-0.4448', '-0.4648', '-0.0792', '-0.03128', '0.03', '0.2013', '-0.04022', '-0.1837', '0.409', '-0.02058', '-0.1332', '0.2563', '0.1249', '-0.501', '-0.3435', '0.2092', '0.0737', '0.521', '0.005547', '0.02788', '0.4458', '-0.1543', '0.3313', '0.3237', '-0.2443', '0.45', '-0.2637', '-0.0607', '-0.1077', '-0.0837', '0.0718', '-0.381', '0.322', '-0.02046', '0.311', '-0.02585', '-0.09717', '-0.1799', '0.2002', '0.18', '-0.2705', '-0.0947', '0.1675', '0.3362', '0.4307', '-0.1554', '0.3599', '0.4077', '-0.2196', '0.01767', '0.3823', '0.8423', '0.1467', '-0.3748', '-0.3262', '0.0666']",,,,,,,
mondo:0015976,hyper-IgM syndrome without susceptibility to opportunistic infections,['HIGM without susceptibility to opportunistic infections'],,,183666,CN200573,"['-0.3726', '-0.06232', '0.1661', '-0.563', '0.044', '-0.02515', '0.144', '-0.01575', '-0.0085', '0.11536', '-0.01551', '0.03043', '-0.1094', '-0.01412', '-0.1108', '-0.0884', '0.1418', '0.1826', '-0.3003', '-0.5024', '0.2312', '-0.3796', '0.7036', '-0.04776', '0.1913', '-0.011734', '0.07764', '0.00579', '-0.1372', '-0.5376', '0.1484', '0.3638', '0.4648', '0.1841', '0.2002', '-0.0951', '-0.6235', '0.1986', '-0.2454', '-0.568', '-0.1812', '-0.00486', '0.2197', '-0.3503', '-0.328', '-0.46', '0.08014', '-0.12146', '-0.134', '0.3013', '0.06824', '-0.01663', '0.4348', '0.0369', '-0.2607', '0.2302', '0.0338', '-0.838', '-0.3564', '0.1117', '0.0871', '0.5703', '-0.0796', '0.1385', '0.3389', '-0.0649', '0.439', '0.3406', '-0.2297', '0.3967', '-0.2893', '-0.003038', '-0.1189', '-0.0974', '0.129', '-0.409', '0.338', '-0.01082', '0.1808', '-0.0877', '-0.2272', '-0.16', '0.1862', '0.1848', '-0.4966', '-0.268', '0.1619', '0.10266', '0.2236', '-0.1344', '0.4695', '0.382', '-0.1508', '-0.03708', '0.6025', '0.6187', '0.1985', '-0.5015', '-0.3694', '0.1267']",,,,,,,
mondo:0015977,agammaglobulinemia,"['Gammaglobulin Deficiency', 'hypogammaglobulinemia', 'mu heavy chain deficiency', 'IGHM', 'antibody Deficiency', 'Immunoglobulin Deficiency']",2583,,183669,,"['0.3813', '0.3896', '-0.3884', '0.02028', '-0.2325', '0.0742', '0.1431', '-0.1237', '-0.3215', '-0.4119', '0.666', '0.1241', '-0.1204', '0.526', '-0.1306', '-0.0655', '-0.185', '0.475', '-0.5117', '-0.4194', '-0.2043', '-0.4001', '0.3796', '0.1152', '0.1787', '-0.872', '-0.3281', '-0.07996', '-0.2927', '-0.1779', '0.6494', '0.03528', '0.6357', '0.04797', '-0.3582', '0.267', '-0.814', '0.12244', '0.1049', '-0.302', '-0.3394', '-0.02869', '0.12024', '-0.657', '-0.3936', '-0.1558', '-0.2651', '-0.4316', '0.2778', '0.3496', '0.0959', '-0.422', '0.2393', '-0.266', '-0.0567', '0.558', '-0.0991', '-0.04965', '-0.1814', '0.2822', '-0.01035', '0.2507', '0.2292', '0.4414', '0.3972', '0.1854', '0.4102', '0.5327', '-1.11', '0.5195', '0.1503', '0.2396', '-0.4182', '-0.01611', '-0.00269', '0.0426', '0.2446', '0.2769', '0.1573', '-0.1505', '-0.2654', '0.0535', '0.09515', '0.0868', '-0.373', '-0.1838', '-0.1519', '-0.4436', '-0.03516', '-0.01116', '0.08203', '0.5054', '-0.4626', '0.1771', '0.3003', '0.5566', '-0.2905', '-0.663', '-0.09015', '0.263']",,,D000361,279.00,,10001471,
mondo:0015978,functional neutrophil defect,"['neutrophilopathy', 'neutrophil disease']",,,183681,,,,,,,,,
mondo:0015979,hereditary predisposition to infections,['genetic susceptibility to infections due to particular pathogens'],,,183710,,,,,,,,,
mondo:0015985,"bone dysplasia, Azouz type",['bone dysplasia Azouz type'],,,1844,C4303993,,,,,,,,
mondo:0015986,bilateral renal agenesis,"['renal agenesis, bilateral', 'bilateral renal aplasia']",0080200,,1848,,,C101219,,,,Q60.1,,
mondo:0015987,scimitar syndrome,"['Halasz syndrome', 'hypogenetic lung syndrome', 'Epibronchial right pulmonary vein syndrome', 'congenital pulmonary venolobar syndrome']",,,185,C0036400,,C85056,,D012587,747.49,,10051951,
mondo:0015988,multicystic dysplastic kidney,"['multicystic renal dysplasia', 'MCDK']",,,1851,C3714581,"['-0.3584', '0.1277', '-0.01686', '0.2108', '-0.0924', '-0.04327', '-0.4927', '0.4526', '-0.469', '-0.4158', '0.1996', '-0.311', '-0.2058', '0.3574', '-0.787', '-0.2078', '0.01363', '-0.1068', '0.3325', '-0.818', '0.155', '0.3413', '0.4993', '-0.3584', '0.3735', '-0.3616', '-0.2223', '0.1936', '0.7075', '-0.1519', '0.489', '-0.45', '0.1985', '0.3735', '0.162', '-0.3677', '-0.002588', '0.3142', '-0.1915', '0.1357', '0.01239', '0.4412', '0.2332', '-0.561', '-0.3926', '-0.03021', '-0.0833', '0.2412', '-0.1444', '0.225', '0.2705', '0.02827', '0.3755', '-0.619', '-0.6357', '-0.254', '0.2463', '-0.3489', '-0.498', '0.533', '0.5483', '0.1362', '-0.1725', '0.3433', '0.1194', '-0.435', '0.5', '0.2445', '-0.1854', '0.5044', '0.3704', '0.243', '0.464', '-0.1455', '-0.329', '-0.1299', '0.1423', '0.2317', '-0.6323', '-0.3823', '-0.4478', '0.1306', '0.2566', '0.0602', '-0.2634', '-0.2893', '0.2365', '-0.2925', '-0.0636', '0.0888', '0.05603', '0.0607', '0.0369', '0.04535', '0.6826', '-0.0697', '0.0057', '-0.3638', '0.01184', '0.4333']",C123031,,D021782,753.19,,,
mondo:0015990,"focal, segmental or multifocal dystonia",,,,1866,,,,,,,G24.5,,
mondo:0015991,citrullinemia,"['deficiency of citrulline-aspartate ligase', 'ass deficiency']",9273,,187,C0175683,,C84639,,D020159,,E72.23,,
mondo:0015993,cone-rod dystrophy,"['CRD', 'cone rod dystrophy', 'cone-rod retinal dystrophy']",0050572,,1872,,,,,D000071700,,H35.5,,
mondo:0015994,muscular dystrophy-white matter spongiosis syndrome,"['muscular dystrophy white matter spongiosis', 'Atrophie blanche']",,,1877,CN200619,,,,,,,,
mondo:0015995,melorheostosis with osteopoikilosis,"['dystrophy osseous sclerosing mixed', 'mixed sclerosing bone dystrophy', 'MSBD syndrome']",,,1879,CN200621,,,,C563593,,,,
mondo:0015997,ectopia lentis-chorioretinal dystrophy-myopia syndrome,"['noble-Bass-Sherman syndrome', 'noble Bass Sherman syndrome', 'ectopia lentis chorioretinal dystrophy myopia']",,,1884,,,,,C536124,,,,
mondo:0015998,isolated ectopia lentis,"['congenital ectopic lens', 'familial ectopia lentis', 'ectopia lentis syndrome', 'IEL', 'nonsyndromic lens position anomaly']",0111148,,1885,,"['-0.569', '-0.0788', '-0.501', '0.3955', '0.6445', '0.04837', '0.002127', '0.8477', '-0.5425', '0.0539', '-0.00756', '-0.4873', '0.2512', '0.5186', '-0.4192', '-0.1276', '0.0779', '-0.381', '0.05573', '-0.8115', '-0.1301', '0.4844', '0.2064', '-0.4146', '-0.4102', '0.478', '-0.732', '0.821', '0.376', '1.21', '0.673', '-0.4795', '0.2817', '0.6504', '-0.1602', '0.11597', '0.0342', '-0.5693', '0.5835', '-0.5713', '0.743', '-0.05673', '0.7974', '-0.2072', '0.105', '-0.0083', '0.483', '-0.2057', '0.104', '-0.04248', '0.3584', '-0.0658', '0.1749', '-0.74', '0.03494', '-0.2625', '0.583', '0.3481', '-0.2462', '0.1492', '0.312', '-0.2356', '-0.04767', '0.1202', '-0.3994', '-0.3447', '0.5986', '0.6216', '-0.0438', '0.2144', '0.02092', '-0.00814', '-0.1539', '-0.1461', '0.3044', '-0.2224', '0.1165', '-0.471', '-0.02118', '0.00365', '0.3035', '0.2527', '0.09717', '0.721', '-0.02107', '0.10803', '-0.01181', '0.3052', '0.09827', '0.5063', '0.1625', '0.7085', '-0.924', '-0.03976', '1.28', '-0.2668', '0.4934', '-0.2361', '0.2888', '-0.02003']",C34566,,C536184,,,10014145,
mondo:0015999,primary pigmented nodular adrenocortical disease,"['pigmented nodular adrenocortical disease, primary', 'pigmented nodular adrenocortical disease', 'primary pigmented nodular adrenal dysplasia', 'PPNAD']",0060280,,189439,CN200645,"['-0.2551', '0.287', '-0.4', '-0.4482', '0.4019', '0.1439', '-0.1316', '0.9316', '-0.5986', '-0.8423', '0.433', '0.1229', '-0.2812', '0.131', '-0.2773', '-0.2443', '0.03244', '0.02867', '-0.2457', '-0.837', '-0.3164', '-0.8477', '0.1838', '-0.3943', '0.559', '0.633', '-0.4333', '-0.612', '-0.5273', '0.1643', '0.2479', '0.107', '-0.0593', '0.4934', '-0.0302', '0.5303', '-0.2374', '0.01628', '-0.3574', '0.33', '0.2927', '-0.557', '0.1946', '-0.3313', '0.4963', '-0.1886', '-0.5615', '0.216', '0.632', '0.5815', '0.299', '-0.05142', '-0.4285', '-0.0814', '-0.923', '-0.1772', '0.6875', '-1.133', '0.0363', '-0.003681', '0.516', '0.2742', '0.1721', '-0.617', '-0.2362', '0.05667', '0.3977', '-0.03677', '0.1065', '0.348', '0.1256', '-0.0548', '1.007', '0.1577', '0.1608', '-0.4563', '-0.4336', '0.359', '-0.6763', '-0.0725', '0.3057', '0.4138', '-0.05798', '-0.3623', '-0.2634', '-0.2053', '0.2585', '-0.2281', '-0.03854', '0.11914', '0.3108', '0.5913', '0.0292', '-0.2478', '0.992', '-0.3704', '0.2854', '-0.6973', '-0.2085', '0.295']",C131196,,,,,,
mondo:0016000,familial isolated hypoparathyroidism due to impaired PTH secretion,,,,189466,CN200646,"['0.02972', '-0.1285', '-0.1946', '-0.00602', '-0.7676', '0.595', '-0.04822', '0.5557', '-1.272', '-0.7217', '-0.2603', '0.1478', '-0.7754', '1.126', '-0.5327', '0.3262', '0.271', '-0.2262', '-0.7695', '-0.5103', '-0.01326', '-0.6377', '-0.0834', '-0.4253', '-0.04443', '-0.4692', '-0.0805', '-0.0921', '0.657', '-0.8247', '-0.48', '0.12494', '-0.3257', '0.0227', '0.01448', '-0.4377', '0.1707', '0.01043', '0.7114', '0.02385', '0.0927', '0.0934', '0.7383', '-0.5347', '0.3774', '-0.4583', '0.565', '0.309', '0.0261', '0.3027', '-0.09235', '0.663', '0.93', '0.1649', '-1.053', '-0.7153', '-0.05215', '-0.5146', '-0.517', '-0.5337', '-0.1603', '-0.534', '0.08563', '-0.2612', '-0.6953', '1.16', '0.5693', '0.946', '-0.727', '0.317', '0.1843', '-0.02295', '0.2598', '-0.582', '0.3276', '0.345', '0.2306', '0.43', '0.327', '0.47', '0.4275', '0.5967', '-0.2301', '-0.8013', '-0.0853', '-0.8613', '-0.3691', '0.1098', '0.7705', '0.294', '0.01393', '0.394', '-0.1631', '0.01317', '0.01933', '0.572', '-0.1302', '-0.9385', '-0.3965', '0.511']",,,,,,,
mondo:0016001,2-hydroxyglutaric aciduria,"['2-HGA', '2-hydroxyglutaric acidemia', '2-hydroxyglutaric aciduria']",0050573,,19,C2746066,"['-0.1602', '0.00812', '-0.3035', '-0.007385', '0.3394', '-0.4097', '-0.2222', '0.531', '-0.5327', '0.0919', '-0.743', '-0.42', '-0.2534', '-0.3767', '0.2844', '0.2644', '0.226', '-0.11566', '-0.3142', '-0.838', '0.511', '0.02374', '0.9624', '-0.0771', '0.1844', '-0.2893', '-0.005424', '-0.2615', '-0.3188', '-0.0504', '0.581', '0.0843', '0.3813', '0.10693', '-0.1012', '-0.312', '-0.781', '0.11774', '-0.309', '0.03235', '0.5347', '-0.9507', '0.3', '-0.44', '0.01393', '-0.6587', '0.5645', '0.003187', '0.3577', '-0.11975', '0.1652', '0.003101', '-0.1971', '-0.523', '-0.2351', '0.0235', '0.05707', '-0.168', '-0.3242', '0.5425', '0.1693', '-0.4192', '0.6196', '-0.1104', '-0.09033', '0.2064', '0.1193', '0.1913', '-0.738', '0.3577', '0.2527', '0.007076', '-0.2817', '0.3606', '0.010956', '0.4915', '0.7754', '-0.1437', '0.07806', '0.0963', '0.2756', '0.03506', '-0.1658', '0.273', '-0.04153', '0.3347', '0.182', '0.1887', '0.1326', '0.1483', '0.4773', '0.2761', '-0.6226', '-0.2295', '0.5186', '0.7056', '0.3079', '-0.01382', '-0.2559', '0.1831']",C128187,,C535306,270.8,,,
mondo:0016002,"Ehlers-Danlos syndrome, kyphoscoliotic type 1","['kEDS', 'Ehlers-Danlos syndrome, type VIA, formerly', 'Ehlers-Danlos syndrome, type VI', 'Ehlers-Danlos syndrome, type 6 A', 'Ehlers-Danlos syndrome, type Via, formerly', 'Ehlers-Danlos syndrome, kyphoscoliosis type', 'kyphoscoliotic Ehlers-Danlos syndrome due to lysyl hydroxylase 1 deficiency', 'EDS 6 (formerly)', 'Ehlers-Danlos syndrome type 6A', 'Ehlers-Danlos syndrome, oculoscoliotic type', 'Ehlers-Danlos syndrome, kyphoscoliotic type', 'nevo syndrome', 'Ehlers-Danlos syndrome, kyphoscoliotic type, 1', 'Ehlers-Danlos syndrome, type VIA', 'EDS, oculoscoliotic type', 'Ehlers-Danlos syndrome type 6 (formerly)', 'EDS 6', 'EDS VIA', 'EDS, kyphoscoliotic type', 'Ehlers-Danlos syndrome oculoscoliotic type', 'EDS VI', 'Ehlers-Danlos syndrome, ocular-scoliotic type', 'kyphoscoliotic EDS', 'Ehlers-Danlos syndrome, type Via', 'Ehlers-Danlos syndrome, type 6', 'EDSKSCL1', 'EDS6', 'EDS6A, formerly', 'kyphoscoliotic Ehlers-Danlos syndrome', 'Ehlers-Danlos syndrome type 6A (formerly)']",0080734,225400,1900,CN202461,"['0.342', '0.07886', '-0.4434', '0.04276', '0.4893', '-0.859', '-0.07996', '0.4487', '-0.9062', '0.672', '0.1816', '-0.1159', '0.3342', '0.9106', '-0.8115', '0.2245', '-0.3237', '0.2028', '0.1641', '-0.4097', '-0.05856', '0.9375', '0.301', '0.1252', '-0.2993', '0.384', '0.1355', '0.3433', '1.489', '0.252', '1.15', '-0.528', '0.4177', '0.1305', '0.0548', '-0.3513', '-0.495', '0.0997', '0.3887', '-1.238', '0.6104', '-0.515', '-0.7803', '0.467', '0.10535', '-0.364', '-0.2764', '0.7627', '0.996', '-0.4512', '0.10645', '-0.452', '0.6216', '-0.267', '0.1638', '-0.666', '-0.4631', '0.7686', '0.2786', '-0.1469', '-0.0747', '0.472', '0.0366', '0.04095', '0.1399', '0.396', '-0.586', '0.936', '-0.2437', '1.115', '-0.653', '0.1962', '-0.2974', '-0.3489', '-0.3428', '-0.3582', '-0.2878', '-0.10645', '0.02805', '-0.371', '-0.04205', '-0.4219', '0.1349', '0.4133', '-0.5796', '0.0634', '0.01531', '0.882', '0.0959', '0.1804', '0.584', '0.7676', '-0.1578', '0.422', '0.503', '-0.2303', '0.5664', '-0.05783', '0.2076', '-0.2255']",C125700,,C536198,,,,
mondo:0016003,ehrlichiosis,['human ehrlichiosis'],10242,,1902,C0085399,,,,D016873,082.40,,,
mondo:0016004,aminopterin/methotrexate embryofetopathy,"['fetal methotrexate syndrome', 'aminopterin fetopathy syndrome', 'foetal aminopterin syndrome', 'aminopterin embryopathy syndrome', 'aminopterin syndrome', 'fetal aminopterin syndrome', 'foetal methotrexate syndrome']",,,1908,C0432367,,C98928,,,759.89,,10071183,
mondo:0016005,indomethacin embryofetopathy,"['foetal indomethacin syndrome', 'antenatal indomethacin exposure', 'fetal indomethacin syndrome']",,,1909,CN200656,,,,,,,,
mondo:0016006,Cockayne syndrome,"['progeria-like syndrome', 'progeroid nanism', 'Cockayne^s syndrome', 'Neill-Dingwall syndrome', 'dwarfism-retinal atrophy-deafness syndrome']",2962,,191,C0009207,"['-0.02734', '0.267', '-0.28', '-0.3245', '0.366', '-0.479', '0.0767', '0.5386', '-0.5737', '-0.0827', '-0.2003', '0.1578', '-0.08844', '0.2905', '-0.149', '-0.03915', '0.7026', '0.05106', '0.2158', '-0.5664', '-0.02394', '-0.1273', '0.1788', '-0.09717', '-0.08215', '0.214', '-0.09863', '0.1908', '0.31', '-0.02084', '0.6045', '0.2742', '0.3508', '-0.2869', '0.1266', '0.3655', '0.1211', '-0.611', '-0.75', '0.01354', '-0.2183', '-0.3337', '0.4421', '0.2573', '-0.181', '-0.602', '0.0262', '0.0765', '0.2113', '-0.03268', '0.0744', '0.0825', '0.0849', '-0.5986', '0.1871', '-0.2505', '0.0713', '-0.4368', '0.1765', '0.06274', '0.1072', '-0.1908', '-0.451', '0.436', '0.1602', '0.1774', '0.2236', '0.5234', '-0.2476', '0.3916', '-0.866', '-0.1059', '0.606', '-0.4521', '0.2467', '0.054', '0.08966', '-0.4292', '0.3655', '0.201', '0.1199', '-0.493', '-1.074', '0.772', '-0.2146', '0.01988', '0.2086', '0.1613', '0.5366', '-0.09424', '0.549', '0.5605', '0.3613', '0.3442', '0.05426', '0.1103', '0.4346', '-0.1783', '0.3674', '0.0184']",C9460,,D003057,759.89,,10009835,
mondo:0016007,cocaine embryofetopathy,"['fetal cocaine syndrome', 'cocaine antenatal exposure', 'prenatal cocaine exposure', 'foetal cocaine syndrome', 'cocaine fetopathy']",,,1911,C0432371,,,,,760.75,,,
mondo:0016008,fetal hydantoin syndrome,"['Dilantin embryopathy', 'phenytoin embryofetopathy', 'fetal dihydantoin syndrome', 'foetal dihydantoin syndrome', 'phenytoin embryopathy', 'FHS']",,,1912,C0265372,,C98927,,C537922,759.89,Q86.1,10016508,
mondo:0016009,fetal trimethadione syndrome,,,,1913,C0265373,,,,C537798,759.89,,,
mondo:0016010,vitamin K-antagonist embryofetopathy,"['embryofetopathy due to oral anticoagulant therapy', 'warfarin embryopathy', 'DiSala syndrome', 'warfarin syndrome', 'vitamin K antagonists embryofetopathy', 'coumarin embryopathy', 'foetal warfarin syndrome', 'congenital warfarin syndrome', 'foetal anticoagulant syndrome', 'vitamin K-antagonist embryopathy', 'fetal Coumadin syndrome', 'di Sala syndrome', 'foetal Coumadin syndrome', 'fetal anticoagulant syndrome', 'coumarin syndrome', 'vitamin K antagonist embryopathy', 'fetal warfarin syndrome', 'warfarin embryofetopathy', 'vitamin K-antagonist embryofetopathy', 'vitamin K antagonist embryofetopathy']",,,1914,C0265374,,C98906,,C536683,759.89,,10051445,
mondo:0016011,fetal alcohol syndrome,"['FASD', 'alcohol-related birth defects', 'static encephalopathy', 'ARND', 'alcohol-related neurodevelopmental disorder', 'foetal alcohol spectrum disorders', 'FAS', 'ARBD', 'fetal alcohol spectrum disorders']",0050667,,1915,C0015923,,C84713,,,,,10016845,
mondo:0016012,diethylstilbestrol syndrome,"['diethylstilbestrol embryofetopathy', 'Distilbene embryofetopathy', 'foetal diethylstilbestrol syndrome', 'DES embryofetopathy', 'antenatal diethylstilbestrol exposure', 'DES syndrome', 'fetal diethylstilbestrol syndrome']",,,1916,C0853695,,C113422,,,,,10012780,
mondo:0016013,fetal methylmercury syndrome,"['Methyl mercury antenatal infection', 'Minamata disease', 'Methyl mercury antenatal exposure']",,,1917,,,,,D020262,759.89,,,
mondo:0016014,fetal minoxidil syndrome,"['minoxidil antenatal exposure', 'minoxidil antenatal infection']",,,1918,C0432373,,,,,760.79,,,
mondo:0016015,phenobarbital embryopathy,['phenobarbital antenatal exposure'],,,1919,C4275281,,,,,,,,
mondo:0016016,toluene embryopathy,"['toluene embryopathy', 'Hersh Podruch Weisskopk syndrome', 'microcephaly, central nervous system dysfunction, minor craniofacial and limb anomalies, and variable growth deficiency']",,,1920,C2931737,,,,C538114,,,,
mondo:0016017,methimazole embryofetopathy,"['MMI/CMZ embryofetopathy', 'foetal methimazole syndrome', 'MMI/CMZ embryopathy', 'Methimazole antenatal exposure', 'methimazole embryofetopathy', 'Methimazole/carbimazole embryopathy', 'Methimazole/carbimazole embryofetopathy', 'fetal methimazole syndrome']",,,1923,C4510379,,,,,,,,
mondo:0016018,diabetic embryopathy,,,,1926,C3830518,,C113485,,,,,,
mondo:0016019,Rasmussen subacute encephalitis,"['RE', 'chronic focal encephalitis', 'CFE', 'Rasmussen syndrome', 'Rasmussen encephalitis']",,,1929,C2930868,,C125384,,C535291,323.9,,,
mondo:0016020,frontal encephalocele,['anterior encephalocele'],,,1931,,,,,,,Q01.0,,
mondo:0016022,early myoclonic encephalopathy,"['myoclonia epileptica', 'myoclonic epilepsy', 'myoclonic seizure', 'early myoclonic encephalopathy', 'early myoclonic encephalopathy with suppression-bursts', 'myoclonic seizure disorder', 'myoclonus epilepsy', 'epileptic seizures - myoclonic', 'epileptic seizures, myoclonic', 'eme']",308,,1935,C0270855,"['0.26', '0.5264', '-0.1271', '-0.1765', '-0.27', '-0.736', '0.3442', '0.821', '-0.515', '-0.2815', '-0.69', '-0.0737', '0.1086', '-0.02214', '0.1776', '-0.05432', '0.2251', '-0.359', '-0.02744', '-1.157', '-0.1099', '0.2477', '0.1033', '-0.4536', '0.01874', '-0.0942', '-0.1619', '-0.4478', '-0.237', '0.3691', '0.2428', '0.0769', '-0.136', '0.4304', '-0.2642', '0.5293', '0.09204', '0.0397', '-0.3699', '0.4688', '-0.06213', '-0.5024', '0.09314', '-0.1637', '0.353', '-0.2268', '-0.549', '0.03079', '-0.04855', '0.4731', '0.01', '0.1987', '-0.3076', '-0.3074', '0.6206', '-0.0659', '0.3574', '-0.06635', '0.1073', '0.0486', '-0.4744', '-0.3093', '0.4407', '-0.5093', '-0.3367', '0.237', '0.8574', '0.9263', '-0.2576', '0.418', '-0.08826', '0.4978', '-0.2676', '-0.06076', '0.2522', '0.11035', '0.1205', '0.1844', '-0.318', '0.01225', '-0.1654', '0.3215', '0.2361', '0.12', '0.679', '-0.1935', '0.2542', '0.3516', '0.512', '0.5786', '0.2507', '0.4697', '-0.01186', '-0.0698', '0.02605', '0.2445', '0.1848', '-0.734', '0.63', '-0.3914']",C116593,1001900,,,,,
mondo:0016024,shoulder and thorax deformity-congenital heart disease syndrome,,,,1940,,,,,,,,,
mondo:0016025,myoclonic-astatic epilepsy,"['myoclonic-astatic epilepsy in early childhood', 'epilepsy with myoclonic-astatic seizures', 'epilepsy with myoclono-astatic crisis', 'mae', 'epilepsy with myoclonic-atonic seizures', 'myoclonic astatic epilepsy', 'Doose syndrome', 'myoclonic atonic epilepsy', 'EMAS']",,,1942,,"['0.999', '0.1738', '-0.3076', '-0.2201', '-0.564', '-0.3042', '1.039', '0.587', '-0.643', '-0.511', '-0.1824', '-0.28', '-0.2255', '0.2262', '-0.1422', '-0.1565', '-0.4146', '-0.512', '-0.1259', '-0.3804', '-0.04443', '0.4978', '0.216', '-0.462', '-0.3015', '-0.3032', '-0.002506', '-0.2338', '-0.5796', '0.1145', '0.116', '-0.826', '0.195', '0.2177', '0.799', '0.2142', '0.1321', '0.2585', '-0.215', '-0.2888', '-0.06537', '-0.3762', '0.04428', '-0.3704', '-0.2225', '-0.7583', '-0.3362', '0.2573', '0.3152', '0.7715', '0.0652', '0.04633', '0.07745', '-0.4055', '-0.01794', '0.07184', '-0.0601', '0.11505', '0.010735', '0.3328', '-0.8276', '0.628', '0.7065', '-0.3794', '-0.2732', '1.392', '0.1844', '-0.0993', '-0.8022', '0.653', '0.8213', '0.6846', '0.07385', '-0.4197', '0.2128', '0.7734', '0.959', '0.2727', '-0.3423', '0.1635', '0.1199', '0.6226', '0.5083', '0.1332', '0.10706', '0.2057', '0.38', '0.58', '0.537', '0.346', '0.0831', '0.2703', '-0.3174', '0.1295', '-0.04135', '0.1393', '0.1919', '-0.583', '0.253', '0.26']",,,,345.10,,,
mondo:0016026,infant epilepsy with migrant focal crisis,,,,1943,C4510564,,,,,,,,
mondo:0016027,benign neonatal seizures,"['benign familal neonatal seizures', 'benign familial neonatal seizures', 'benign familial convulsions', 'BFNS', 'seizures, benign familial neonatal', 'benign neonatal convulsions', 'benign familial convulsion', 'benign familial neonatal convulsions']",14264,,1949,,"['0.2546', '0.07367', '-0.4182', '0.3262', '-0.7124', '-0.5063', '0.802', '0.6675', '-0.2103', '-0.4204', '-0.2686', '-0.1823', '0.135', '0.6587', '-0.3687', '0.1049', '-0.1732', '-0.3235', '-0.0692', '-0.4587', '0.05902', '0.56', '0.1852', '-0.2037', '0.09875', '-0.05685', '-0.272', '0.0761', '-0.318', '0.3513', '0.2854', '-0.02206', '0.1283', '0.2551', '0.313', '0.4062', '0.0709', '-0.4707', '0.0631', '-0.2986', '-0.2275', '-0.2482', '0.05847', '-0.4153', '0.0749', '-0.09735', '-0.345', '0.418', '-0.07733', '0.98', '0.00257', '0.0784', '-0.0827', '-0.5283', '0.1178', '0.2808', '-0.0795', '-0.1355', '0.0308', '0.03128', '0.25', '0.463', '0.4624', '-0.04944', '-0.5415', '0.988', '0.291', '-0.171', '-0.5664', '0.789', '0.593', '0.4966', '0.0742', '-0.2808', '0.4846', '0.7344', '0.566', '0.0978', '-0.409', '-0.04214', '0.0813', '0.663', '0.617', '-0.0848', '0.4146', '0.1019', '0.2444', '0.611', '0.6357', '0.7666', '0.3264', '0.1687', '-0.04385', '-0.02525', '-0.1186', '0.03998', '0.3372', '-0.7466', '0.56', '0.2413']",C117307,,,,,10067866,
mondo:0016028,erythromelalgia,,9240,,1956,C0014804,,C34593,,D004916,443.82,I73.81,10015284,
mondo:0016029,esthesioneuroblastoma,['olfactory neuroblastoma'],,,1957,,,,,,,,,
mondo:0016030,Evans syndrome,"['autoimmune hemolytic anemia and autoimmune thrombocytopenia', 'autoimmune hemolytic anaemia and autoimmune thrombocytopenia', 'Evans^ syndrome', 'immune pancytopenia', 'Evan syndrome']",8931,,1959,C0272126,,C61284,,C536380,287.32,D69.41,10053873,
mondo:0016031,facial dysmorphism-anorexia-cachexia-eye and skin anomalies syndrome,"['facial features (unique), anorexia, cachexia, eye and skin anomalies', 'faces syndrome', 'Friedman-Goodman syndrome']",,,1969,C2931183,,,,C536384,,,,
mondo:0016032,femoral agenesis/hypoplasia,"['femoral intercalary meromelia', 'congenital short femur']",,,1987,,,,,,755.34,,,
mondo:0016033,Cornelia de Lange syndrome,"['CDLS', 'Brachmann de Lange syndrome', 'Brachmann-de Lange syndrome', 'De Lange syndrome']",11725,,199,CN239271,"['0.3652', '0.3584', '0.422', '-0.491', '0.382', '-0.294', '-0.1594', '0.666', '-0.9946', '-0.721', '-0.03555', '-0.1133', '0.3071', '-0.29', '-0.399', '0.4517', '0.4207', '-0.4243', '-0.3286', '-0.656', '-0.1079', '-0.00943', '0.2146', '-0.1544', '0.6597', '-0.2092', '-0.0411', '0.2969', '0.6143', '-0.1005', '0.4958', '-0.2927', '0.0488', '0.6294', '-0.521', '0.1943', '0.3298', '0.1707', '0.04102', '-0.001684', '-0.1783', '-0.2808', '0.3184', '-0.485', '0.1997', '-0.861', '-0.2278', '0.09735', '0.1996', '0.03506', '-0.471', '0.1051', '-0.537', '-0.5854', '0.00833', '-0.4478', '0.0821', '0.3933', '0.1709', '0.2715', '-0.2473', '-0.013794', '-0.2964', '-0.102', '0.3206', '0.2537', '0.389', '0.1855', '-0.178', '0.4102', '-0.4495', '-0.1892', '-0.05267', '0.2162', '0.01289', '0.1599', '0.55', '0.0337', '-0.503', '0.3943', '0.3694', '-0.1516', '0.2102', '0.4138', '0.10864', '0.362', '-0.3015', '0.258', '0.05487', '0.5537', '-0.289', '-0.08154', '-0.2085', '0.2389', '0.604', '0.00204', '0.2192', '-0.7573', '0.56', '0.5137']",C75016,,,,,10056354,
mondo:0016034,cleft lip with or without cleft palate,"['Tessier cleft number 1,2']",,,1991,,,,,,,,,
mondo:0016035,Nelson syndrome,"['Ridges-off-the-end syndrome', 'dermal Ridges', 'Nelson^s syndrome']",4968,125530,199244,C0027577,,C84917,,D009347,,,10028913,
mondo:0016037,superficial Fibromatosis,['superficial Fibromatosis'],,,199257,C0406571,,C6814,1000556,,729.99,,,
mondo:0016038,calcified aponeurotic fibroma,"['Juvenile aponeurotic fibrosis', 'Keasby tumour', 'Juvenile aponeurotic fibroma', 'juvenile aponeurotic fibromatosis', 'calcifying aponeurotic fibroma', 'Keasby tumor']",,,199260,C0553647,,C4818,,,,,,
mondo:0016039,infantile digital fibromatosis,"['inclusion body fibromatosis', 'recurring digital fibrous tumour of childhood', 'Reye tumour', 'IDF', 'digital fibrous tumor of Reye', 'recurring digital fibrous tumor of childhood', 'asymptomatic nodular proliferation of fibrous tissue on the dorsal and lateral aspects of the fingers or toes', 'digital fibrous tumour of Reye', 'Reye^s tumour', 'inclusion body fibromatosis (disease)', 'infantile digital fibroma/fibromatosis', 'Reye tumor', 'infantile digital fibromatosis', 'Reye^s tumor']",,,199267,C1318562,,C3456,1000301,,238.8,,,0025197
mondo:0016040,harlequin syndrome,"['sudden onset of unilateral flushing and sweating', 'progressive isolated segmental anhidrosis', 'unilateral loss of facial flushing and sweating with contralateral anhidrosis']",,,199282,C2029348,,,,C535634,705.89,,,
mondo:0016041,congenital microgastria,,,,199293,,,,,,750.7,,,
mondo:0016042,late-onset isolated ACTH deficiency,,,,199299,,,,,,,,,
mondo:0016043,isolated cleft lip,['nonsyndromic cleft lip (disease)'],,,199302,,,,,,,,10009259,
mondo:0016044,cleft lip/palate,"['cleft lip and palate', 'cleft lip-alveolus-palate syndrome', 'alveolar cleft lip and palate', 'FLP']",,,199306,,,,,,749.25,Q35-Q37,10009260,
mondo:0016045,tetragametic chimerism,"['46,XX/46,XY chimerism']",,,199310,CN200724,,,,,,,,
mondo:0016046,familial clubfoot with or without associated lower limb anomalies,,,,199315,CN200725,"['-0.1472', '-0.2482', '0.6', '0.3647', '0.1814', '-0.3193', '-0.3247', '0.804', '-1.122', '-0.8267', '0.4846', '0.1642', '-0.0827', '0.907', '0.2', '-0.03967', '-0.545', '-0.03061', '0.02724', '-1.069', '0.0942', '0.8506', '0.03738', '-0.3455', '-0.2186', '0.09625', '0.07684', '0.307', '0.458', '-0.03384', '0.3005', '-0.3872', '0.1414', '0.4688', '-0.03845', '0.0978', '-0.1935', '-0.4043', '0.4778', '-0.434', '0.696', '0.842', '-0.4763', '0.5117', '0.11414', '0.686', '0.097', '0.0472', '-0.1677', '0.1433', '-0.2815', '-0.6626', '0.4126', '-0.1136', '-0.657', '0.3823', '-0.9937', '-0.3564', '-0.428', '-0.1259', '0.5435', '0.2181', '-0.05292', '0.3853', '-0.1572', '0.9263', '0.1534', '0.05176', '-0.0473', '0.6343', '-0.1057', '0.79', '0.3088', '-0.3745', '0.3262', '0.5537', '-0.1669', '-0.0633', '-0.2197', '-0.4438', '-0.2272', '0.2212', '0.6665', '0.7314', '0.426', '0.1058', '0.11945', '-0.1394', '0.9473', '-0.12054', '-0.203', '-0.00493', '0.158', '0.1915', '0.5537', '0.1886', '0.5117', '-0.395', '-0.00534', '-0.287']",,,,,,,
mondo:0016047,endophthalmitis,,4692,,199323,C0014236,,C34586,,D009877,360.19,,10014801,
mondo:0016048,"isolated autosomal dominant hypomagnesemia, Glaudemans type",,,,199326,CN200728,,,,,,,,
mondo:0016049,"congenital myopathy, Paradas type",,,,199329,,,,,,,,,
mondo:0016051,cleft lip-retinopathy syndrome,"['Ausems-Wittebol Post-Hennekam syndrome', 'Ausems Wittebol-Post Hennekam syndrome', 'cleft lip-cone rod dystrophy syndrome', 'cleft lip with progressive retinopathy', 'cleft lip-progressive retinopathy syndrome']",,,1995,C2931789,,,,C538272,,,,
mondo:0016052,atypical autism,,0060042,,199627,,,,,,299.80,,10003747,
mondo:0016053,isolated cerebellar vermis hypoplasia,,,,199630,,,,,,,,,
mondo:0016054,cerebral malformation,['brain malformation'],,,199633,,,,,,,,,
mondo:0016056,isolated congenital microcephaly,"['microcephaly, primary', 'true microcephaly', 'primary microcephaly']",0070297,,199642,,,,,,,,10027534,
mondo:0016057,isolated encephalocele,"['bifid cranium', 'encephalocele', 'cranium bifidum', 'craniocele']",,,199647,,,,,,,,10014617,
mondo:0016058,paroxysmal dystonia,,,,200037,,,,,,333.99,,,
mondo:0016059,cleft lip/palate-deafness-sacral lipoma syndrome,['Lowry-Yong syndrome'],,,2003,CN200748,,,,,,,,
mondo:0016060,laryngotracheoesophageal cleft,"['laryngo-tracheo-esophageal diastema', 'LTEC', 'Larnygeotracheoesophageal cleft', 'laryngo-tracheo-esophageal cleft', 'congenital cleft larynx', 'laryngeal cleft', 'LC', 'tracheal cleft']",,,2004,,,C98622,,C537875,,,,
mondo:0016061,immunodeficiency with factor H anomaly,,,,200421,,"['-0.076', '0.5557', '-0.4028', '0.04745', '-0.2952', '-0.007053', '0.2391', '-0.5107', '0.01944', '-0.541', '-0.2268', '0.1854', '-0.1367', '0.1366', '0.05255', '-0.1675', '-0.3608', '0.1367', '-0.3682', '-0.673', '0.1609', '-0.369', '0.848', '-0.02824', '0.5767', '0.1934', '-0.07056', '0.0836', '-0.2141', '-0.2108', '0.3672', '0.5376', '0.488', '0.4146', '0.03656', '0.0923', '-0.4038', '0.03693', '-0.5615', '-0.1664', '-0.365', '0.3306', '0.2546', '-0.2737', '0.08246', '-0.609', '-0.04495', '-0.1674', '0.116', '0.8125', '-0.0763', '0.03394', '0.1317', '-0.11285', '-0.3865', '-0.11035', '-0.02583', '-0.2554', '-0.2532', '0.2932', '0.04266', '0.4375', '-0.0304', '0.3943', '0.2512', '0.09814', '0.3667', '0.3289', '-0.2335', '0.4395', '-0.7915', '-0.05463', '-0.05124', '-0.2107', '0.3198', '-0.2559', '0.349', '0.2534', '0.1963', '0.01264', '-0.09686', '-0.2441', '0.474', '0.4', '-0.3923', '-0.1799', '0.2089', '0.1788', '-0.1637', '-0.1029', '0.548', '0.2448', '0.05026', '-0.11523', '0.3987', '0.887', '0.1067', '-0.5884', '-0.3323', '0.01851']",,,,,,,
mondo:0016062,median cleft lip/mandibule,['median cleft lower facial stage'],,,2006,,,,,,,,,
mondo:0016063,Cowden disease,"['Cowden syndrome', 'multiple hamartoma syndrome', 'Cowden^s disease', 'Cowden disease', 'MHAM', 'CD', 'dysplastic gangliocytoma of cerebellum']",6457,,201,C0391826,"['0.273', '0.51', '-0.1997', '0.1713', '0.1715', '-0.3267', '-0.337', '0.764', '-0.1476', '-0.6694', '0.0906', '0.5386', '0.349', '-0.01599', '0.2751', '0.1164', '-0.1792', '-0.4634', '-0.1655', '-0.3833', '0.0839', '-0.4436', '0.5166', '0.12286', '0.856', '-0.4268', '-0.1506', '0.00874', '0.2764', '-0.509', '1.026', '-0.4514', '0.1885', '-0.2913', '0.4678', '0.4739', '-0.7197', '-0.1539', '-0.005966', '0.5845', '-0.1156', '-0.2646', '0.6187', '-0.1866', '0.8516', '-0.5557', '0.0878', '0.3008', '0.1056', '-0.6865', '0.1493', '0.6475', '-0.316', '-0.04605', '-0.1897', '-0.1117', '0.3586', '0.01076', '-1.142', '0.2151', '0.761', '0.228', '-0.113', '0.0931', '0.3047', '0.2104', '0.3062', '0.0478', '-0.3147', '0.823', '0.3179', '-0.1611', '-0.3643', '-0.00268', '-0.0002756', '-0.693', '-0.169', '-0.2778', '-0.77', '-0.2542', '0.04294', '0.5547', '0.2646', '0.11957', '-0.1868', '-0.3948', '0.4163', '0.2551', '0.3303', '-0.463', '0.2778', '0.763', '0.0701', '-0.1562', '-0.1305', '-0.4863', '0.2766', '-0.265', '0.1895', '-0.2377']",C8419,,D006223,,,10051906,
mondo:0016064,cleft palate,"['palatoschisis', 'uranostaphyloschisis']",674,,2014,C0008925,,C87069,,D002972,749.00,,10009269,
mondo:0016065,cleft palate-short stature-vertebral anomalies syndrome,"['Mathieu-De Broca-Bony syndrome', 'cleft palate short stature vertebral anomalies']",,,2015,CN200784,,,,,,,,
mondo:0016066,sternal cleft,"['cleft sternum', 'sternum bifidum', 'congenital sternal cleft']",,,2017,C2931507,,,,C537489,756.3,,,
mondo:0016067,Crandall syndrome,"['alopecia-sensorineural deafness-hypogonadism syndrome', 'alopecia deafness hypogonadism', 'alopecia-deafness-hypogonadism syndrome']",,,202,C0432348,,,,,704.8,,,
mondo:0016068,fibrochondrogenesis,,0060465,,2021,,"['-0.1847', '0.2332', '-0.4182', '-0.314', '0.2568', '-0.358', '-0.008896', '0.8066', '-0.4976', '-0.577', '0.446', '-0.1127', '-0.0744', '-0.01446', '-0.03485', '0.7563', '0.4548', '-0.1355', '-0.5054', '-0.1609', '-0.6216', '0.1604', '0.753', '-0.2338', '-0.1582', '-0.225', '-0.4932', '0.0859', '0.75', '-0.3328', '0.2034', '-0.9136', '0.27', '-0.007328', '0.533', '0.01155', '-0.002523', '-0.3015', '-0.0688', '-0.395', '-0.2319', '-0.502', '-0.2115', '-0.589', '-0.497', '-0.3455', '-0.4148', '0.586', '-0.479', '0.1353', '-0.1344', '-0.5435', '-0.442', '0.2964', '-0.609', '-0.5825', '0.09717', '-0.1141', '0.04214', '-0.1565', '0.09845', '-0.0913', '-0.225', '0.3074', '-0.327', '-0.2703', '-0.02296', '0.1831', '0.05414', '0.694', '-0.558', '0.3367', '0.0526', '-0.129', '-0.10376', '0.5674', '-0.0386', '0.1481', '-0.2155', '-0.00521', '-0.1324', '0.3108', '0.3909', '0.4053', '0.2241', '-0.03668', '-0.353', '0.2686', '-0.0918', '-0.263', '-0.3188', '-0.07574', '0.00679', '0.2494', '1.103', '0.3594', '0.4705', '-0.952', '0.1705', '0.1387']",,,C562524,,,,
mondo:0016070,hereditary gingival fibromatosis,"['hereditary gingival hyperplasia', 'autosomal dominant gingival fibromatosis', 'hereditary gingival fibromatosis', 'autosomal dominant gingival hyperplasia']",0060466,,2024,C0399440,"['-0.11383', '0.2236', '0.0573', '-0.2866', '0.2465', '-0.0725', '-0.0541', '0.01258', '-0.3594', '0.1843', '-0.1913', '0.1068', '-0.2952', '0.08405', '0.09796', '0.1528', '0.04114', '-0.286', '-0.06915', '-0.568', '-0.1289', '-0.0792', '0.382', '-0.1592', '0.258', '0.1327', '-0.162', '-0.0825', '0.1257', '-0.1327', '0.1403', '-0.00832', '-0.1404', '0.2189', '0.1688', '-0.1113', '-0.2029', '-0.03574', '-0.02177', '-0.2683', '0.1842', '-0.337', '0.02452', '-0.0521', '0.05182', '-0.2435', '-0.3516', '0.2474', '0.10535', '-0.03226', '0.2695', '0.0466', '0.1177', '-0.12146', '-0.3909', '-0.3225', '0.1726', '-0.04663', '-0.1362', '-0.1912', '0.117', '0.0056', '-0.0002425', '-0.0833', '-0.1094', '0.1595', '0.4553', '0.4675', '-0.05518', '0.06018', '-0.2467', '-0.006626', '0.4912', '-0.1553', '-0.05115', '-0.1794', '0.0372', '0.3704', '-0.1414', '-0.4763', '-0.3245', '0.02815', '-0.08276', '-0.03253', '-0.031', '0.0607', '-0.08246', '0.02124', '0.02231', '0.05017', '-0.0112', '0.3323', '0.3674', '0.3003', '0.522', '-0.1278', '0.3467', '-0.3806', '0.1503', '0.1833']",,,,,,,
mondo:0016071,juvenile hyaline fibromatosis,"['Puretic syndrome', 'Molluscum fibrosum', 'mesenchymal dysplasia', 'Murray-Puretic-Drescher syndrome']",,,2028,,"['-0.4158', '0.2664', '0.2678', '-0.2705', '-0.1915', '-0.186', '-0.196', '0.2734', '-0.9697', '0.1472', '-0.1606', '0.10034', '-0.3755', '-0.05756', '0.3586', '0.3955', '-0.0937', '-0.3835', '-0.1688', '-0.4465', '0.3647', '-0.5225', '0.2406', '-0.3506', '0.334', '0.399', '0.00863', '0.1897', '-0.0962', '-0.624', '-0.1772', '0.2468', '-0.1781', '0.2793', '0.1533', '-0.001731', '-0.2206', '0.2313', '0.1103', '-0.7827', '0.3655', '-0.781', '-0.2808', '0.3123', '-0.10803', '-0.1197', '-0.101', '0.2283', '0.391', '0.3486', '-0.04184', '0.2378', '0.795', '0.5635', '-0.25', '-0.1876', '0.04202', '0.2096', '-0.3455', '0.001574', '0.3557', '0.07745', '-0.54', '-0.5674', '0.0081', '0.04132', '0.469', '0.717', '-0.0695', '-0.2145', '-0.2416', '-0.1989', '-0.1897', '-0.247', '-0.1854', '-0.326', '0.158', '0.53', '-0.3103', '-0.4482', '-0.5747', '0.10754', '0.2229', '0.0117', '-0.5244', '-0.1992', '-0.3281', '0.02191', '0.397', '-0.0829', '0.5864', '0.9473', '0.05075', '0.2954', '0.3948', '0.2988', '0.3884', '-0.1562', '0.424', '0.0957']",C98297,,,733.29,,,
mondo:0016072,anomaly of puberty or/and menstrual cycle of genetic origin,['genetic anomaly of puberty or/and menstrual cycle'],,,202940,,,,,,,,,
mondo:0016073,syndromic microphthalmia,"['syndrome associated with microphthalmia', 'syndromic microphthalmia', 'microphthalmia, syndromic']",0080636,,202948,CN226833,"['-0.0805', '0.008286', '0.014885', '-0.0684', '0.1398', '-0.1373', '0.09515', '0.1019', '-0.1743', '-0.153', '-0.02635', '-0.0797', '-0.0168', '0.03735', '-0.0444', '-0.0723', '0.0221', '-0.04114', '0.03021', '-0.3208', '0.000547', '0.0197', '0.052', '-0.0667', '0.08344', '0.05032', '-0.04123', '0.01753', '0.10596', '0.02612', '0.1411', '-0.051', '0.2043', '0.06866', '0.12036', '0.011246', '0.02982', '-0.131', '-0.0393', '-0.207', '0.1165', '-0.0966', '0.00806', '-0.1317', '0.01744', '-0.1713', '0.00813', '0.0855', '0.05734', '-0.0752', '0.0008125', '-0.1133', '-0.02798', '-0.07574', '-0.12445', '-0.05893', '0.09045', '-0.0654', '-0.1821', '0.01923', '-0.02332', '0.02719', '0.09344', '0.02711', '-0.0663', '0.0714', '0.1504', '0.1489', '-0.1357', '0.1642', '-0.1608', '0.1027', '0.05423', '-0.06757', '0.1027', '0.00863', '0.06915', '-0.03053', '-0.10364', '-0.1351', '-0.05603', '0.0949', '-0.1339', '0.2795', '-0.022', '-0.1622', '0.04108', '0.1328', '0.08417', '0.0858', '0.0685', '0.2115', '0.0754', '0.116', '0.395', '-0.004795', '0.07996', '-0.1627', '0.0944', '0.089']",,,,,,,
mondo:0016075,filariasis,['disease due to superfamily Filarioidea'],1080,,2034,C0016085,,C34611,,D005368,125.9,B74,10016674,
mondo:0016077,congenital aortopulmonary window,"['congenital aortopulmonary septal defect', 'aorto-pulmonary artery fistula', 'aortopulmonary fistula', 'aorta-pulmonary artery fistula', 'congenital aortopulmonary artery fistula']",,,2037,C2931610,,,,C537782,,,,
mondo:0016078,congenital systemic arteriovenous fistula,,,,2039,,,,,,,,,
mondo:0016079,sporadic Creutzfeldt-Jakob disease,['sporadic CJD'],,,204,,,,,,046.19,,10011384,
mondo:0016080,congenital bronchobiliary fistula,,,,2040,,,,,,,,,
mondo:0016081,coronary arterial fistulas,"['Coronaro-cardiac fistula', 'coronary arterial malformations']",,,2041,,,,,,,,10069441,
mondo:0016083,FLOTCH syndrome,"['familial occurrence of total leukonychia, trichilemmal cysts and ciliary dystrophy with dominant autosomal heredity', 'leukonychia totalis-trichilemmal cysts-ciliary dystrophy syndrome']",,,2045,C2931411,,,,C537065,,,,
mondo:0016085,Cole-Carpenter syndrome,"['bone fragility-craniosynostosis-proptosis-hydrocephalus syndrome', 'Cole Carpenter syndrome']",0060438,,2050,C1862178,"['-0.37', '-0.2467', '0.587', '-0.6025', '0.555', '-0.3728', '-0.0989', '0.5415', '-0.3877', '-0.06793', '-0.1667', '-0.0904', '0.08545', '-0.2507', '-0.258', '-0.08325', '0.4941', '-0.0634', '0.04062', '-0.6553', '0.0353', '-0.0924', '0.651', '-0.1283', '0.2607', '0.375', '-0.1833', '-0.4917', '0.526', '0.03076', '-0.1903', '0.0351', '0.2554', '0.2446', '-0.3203', '-0.10895', '-0.1393', '-0.583', '-0.3652', '-1.019', '0.1223', '-0.297', '0.2722', '-0.488', '-0.1445', '-0.8984', '0.1311', '0.415', '0.4978', '-0.2625', '0.1799', '-0.3054', '0.4902', '-0.0353', '-0.2712', '-0.842', '-0.397', '0.02307', '-0.2527', '0.1154', '0.2139', '-0.1128', '-0.5923', '-0.03915', '-0.1255', '-0.16', '-0.0724', '0.3347', '-0.627', '0.4143', '-0.2993', '-0.00763', '0.1401', '-0.05325', '-0.12177', '0.274', '0.08234', '0.02432', '0.3066', '-0.4055', '-0.0859', '-0.2808', '-0.1812', '0.565', '-0.481', '0.2072', '0.137', '0.349', '0.64', '-0.02917', '-0.309', '0.375', '0.4065', '0.17', '0.2462', '0.656', '0.596', '-0.07635', '0.2988', '0.2083']",C130985,,C535963,,,,
mondo:0016086,osteochondritis of tarsal/metatarsal bone,"['osteochondritis of tarsal/metatarsal bone', 'navicular Osteochondrosis', 'Kohler^s disease', 'aseptic necrosis of the tarsal bone', 'Kohler^s disease of the tarsal navicular', 'Kohler disease', 'juvenile osteochondrosis of foot', 'Kohler^s Osteochondrosis of the tarsal navicular', 'Osteochondrosis of the tarsal bone']",11760,,563991,CN200840,,,,,732.5,,,
mondo:0016087,progressive non-infectious anterior vertebral fusion,['Copenhagen syndrome'],,,2062,CN200850,,,,,,,,
mondo:0016088,hypoxanthine-guanine phosphoribosyltransferase deficiency,"['HPRT1 deficiency', 'hypoxanthine-guanine phosphoribosyltransferase 1 deficiency', 'HPRT deficiency']",,,206428,,,,,,277.6,,,
mondo:0016089,infantile Krabbe disease,"['Krabbe disease, classic form', 'Krabbe disease, early-onset']",,,206436,,,,,,,,,
mondo:0016090,late-infantile/juvenile Krabbe disease,"['Krabbe disease, late-onset']",,,206443,CN200855,,,,,,,,
mondo:0016091,adult Krabbe disease,['Krabbe disease of adults'],,,206448,CN200856,,,,,,,,
mondo:0016092,serous or mucinous cystadenoma of childhood,"['serous cystadenoma of ovary in childhood', 'mucinous cystadenoma of ovary in childhood']",,,206470,,,,,,,,,
mondo:0016093,borderline epithelial tumor of ovary,"['borderline ovarian epithelial neoplasm', 'ovarian tumour of low malignant potential', 'ovarian tumours of low malignant potential', 'borderline ovarian surface epithelial-stromal tumor', 'epithelial tumour of the ovary of borderline malignancy', 'borderline epithelial neoplasm of the ovary', 'borderline epithelial neoplasm of ovary', 'low malignant potential ovarian tumor', 'borderline ovarian epithelial tumour', 'low malignant potential ovarian tumour', 'ovarian tum. of low malig. poten.', 'borderline epithelial tumor of ovary', 'epithelial tumor of ovary of borderline malignancy', 'ovarian tumors of low malignant potential', 'borderline epithelial tumor of the ovary', 'epithelial ovarian tumor of borderline malignancy', 'epithelial neoplasm of the ovary of borderline malignancy', 'ovarian tumor of low malignant potential', 'ovarian low malignant potential tumour', 'epithelial ovarian neoplasm of borderline malignancy', 'epithelial tumor of the ovary of borderline malignancy', 'epithelial neoplasm of ovary of borderline malignancy', 'borderline ovarian epithelial tumor', 'ovarian borderline malignant tumour', 'borderline ovarian surface epithelial-stromal tumour', 'ovarian borderline malignant tumor', 'epithelial tumour of ovary of borderline malignancy', 'ovarian low malignant potential tumor', 'borderline epithelial tumour of the ovary', 'epithelial ovarian tumour of borderline malignancy']",,,206473,C3665489,,C4783,1000140,,,,,
mondo:0016094,vaginal germ cell malignant tumor,"['vagina malignant germ cell tumour', 'malignant germ cell tumour of the vagina', 'vaginal germ cell cancer', 'vagina malignant germ cell tumor', 'malignant germ cell tumor of the vagina']",,,206489,CN200860,,,,,,,,
mondo:0016095,vaginal rhabdomyosarcoma,"['vagina rhabdomyosarcoma (disease)', 'vaginal rhabdomyosarcoma', 'vulvovaginal rhabdomyosarcoma']",,,206492,C4288035,,C128080,,,,,,
mondo:0016096,malignant non-dysgerminomatous germ cell tumor of ovary,"['ovarian Nondysgerminomatous germ cell tumour', 'non-dysgerminomatous germ cell cancer of ovary', 'ovarian non-dysgerminomatous germ cell tumor', 'ovarian non-dysgerminomatous germ cell tumour', 'ovarian Nondysgerminomatous germ cell tumor']",,,206538,CN200863,,C102870,,,,,,
mondo:0016097,symptomatic form of muscular dystrophy of Duchenne and Becker in female carriers,,,,206546,CN200864,,,,,,,,
mondo:0016098,immune-mediated necrotizing myopathy,"['immune myopathy with myocyte necrosis', 'NAM', 'IMNM', 'necrotizing autoimmune myopathy', 'anti-HMG-CoA myopathy', 'anti-SRP myopathy', 'autoimmune necrotizing myositis']",,,206569,,,,,,,,,
mondo:0016099,overlap myositis,"['adult-onset overlap myositis', 'non-specific myositis']",,,206572,,,,,,,,,
mondo:0016100,rippling muscle disease with myasthenia gravis,"['Rmd-MG', 'acquired rippling muscle disease', 'immune-mediated rippling muscle disease']",,,206575,CN200870,,,,,,,,
mondo:0016101,neurolymphomatosis,"['fowl paralyses', 'Marek^s disease', 'Marek disease', 'fowl paralysis', 'fowl paralyzes']",,,206586,C0024793,,,,D008380,,,,
mondo:0016102,subacute inflammatory demyelinating polyneuropathy,"['SIDP', 'subacute inflammatory demyelinating polyradiculoneuropathy']",,,206594,C0456517,,,,,,,,
mondo:0016103,isolated asymptomatic elevation of creatine phosphokinase,"['isolated hyperCKemia', 'idiopathic asymptomatic hyperCKemia', 'isolated asymptomatic hyperCKemia', 'hyperCKmia']",0111338,,206599,,"['-0.3923', '-0.1649', '-0.7876', '-0.2869', '0.05923', '0.03098', '0.1028', '0.366', '-0.3062', '-0.4297', '0.268', '0.2615', '0.0007677', '0.128', '-0.02045', '0.2145', '-0.3855', '-0.2343', '-0.4705', '-0.6724', '0.4102', '-0.10486', '0.2861', '0.484', '0.3518', '0.01726', '-0.1248', '-0.1345', '-0.2002', '0.1787', '0.4417', '-0.4321', '0.287', '0.314', '0.129', '-0.1172', '-0.3057', '0.1996', '0.3435', '-0.5996', '-0.02168', '-0.353', '-0.1483', '-0.2482', '0.2703', '0.0687', '0.2067', '0.02791', '-0.07837', '0.3066', '0.1309', '-0.2922', '0.1798', '-0.3484', '0.03534', '-0.0998', '0.3416', '-0.4368', '-0.2218', '-0.0496', '0.3228', '0.1821', '0.2786', '-0.2455', '-0.2408', '0.1015', '0.09607', '0.0953', '-0.483', '-0.06046', '-0.2028', '0.2283', '0.05847', '0.3057', '0.3838', '0.1819', '0.3574', '0.3535', '0.02658', '-0.2448', '0.5083', '0.4048', '0.2192', '-0.054', '-0.2472', '0.01379', '0.0776', '0.1451', '0.2935', '-0.0673', '0.3994', '-0.08234', '-0.1501', '-0.2455', '0.597', '0.5366', '-0.3577', '-0.307', '-0.602', '0.07715']",C148327,,,,,,
mondo:0016105,acquired skeletal muscle disease,['acquired skeletal muscle disease'],,,206638,CN200878,,,,,,,,
mondo:0016106,progressive muscular dystrophy,,,,206644,CN241791,,,,,,,,
mondo:0016107,myotonic dystrophy,"['inherited myotonic dystrophy', 'myotonia atrophica', 'myotonic disease', 'myotonia dystrophica']",450,,206647,C0027126,"['-0.5044', '0.2024', '0.08795', '-0.4343', '0.1254', '-0.08405', '0.1043', '0.2903', '-0.3496', '-0.4753', '-0.0885', '-0.07935', '-0.2361', '-0.0597', '-0.01065', '0.0669', '-0.03192', '0.05136', '-0.2', '-0.4407', '0.3335', '-0.1127', '0.1389', '0.4348', '0.05945', '-0.00593', '0.0991', '-0.3945', '0.1583', '-0.0397', '0.3843', '0.3408', '0.3938', '0.011055', '-4.74e-05', '0.10895', '0.0736', '-0.0689', '-0.2047', '-0.2812', '0.01032', '-0.1583', '0.2457', '0.3853', '0.1965', '-0.0374', '0.1165', '0.2942', '0.1685', '0.00969', '0.3015', '0.215', '0.0665', '-0.1945', '-0.02684', '-0.3955', '0.4033', '-0.05676', '-0.236', '0.1056', '0.10236', '-0.00202', '0.2742', '-0.0887', '0.1067', '-0.07416', '0.197', '0.553', '-0.5225', '-0.10834', '-0.4988', '-0.1985', '0.1375', '0.09515', '0.4355', '0.1815', '-0.04352', '0.12476', '-0.11914', '-0.2766', '0.4966', '-0.06866', '-0.01111', '-0.05994', '-0.2708', '0.2313', '0.3645', '0.1895', '0.446', '0.2385', '-0.11273', '0.1628', '0.2998', '-0.02068', '0.5493', '0.1362', '0.278', '-0.2122', '-0.2585', '0.1204']",C84914,,D009223,359.2,,10068871,
mondo:0016108,autosomal dominant distal myopathy,"['distal myopathy, autosomal dominant']",,,206650,CN229018,"['-0.3901', '-0.2935', '0.1403', '-0.096', '0.2551', '-0.574', '0.1976', '0.3354', '-0.2534', '-0.3545', '-0.0637', '0.01772', '-0.02135', '0.1771', '0.1155', '-0.1248', '-0.1522', '-0.186', '-0.253', '-0.975', '0.1387', '0.02686', '0.1086', '0.685', '-0.1367', '-0.1658', '-0.2255', '-0.434', '-0.2788', '-0.4805', '0.0259', '0.07764', '0.1869', '-0.08636', '0.11115', '-0.2073', '-0.2443', '-0.0996', '0.0961', '-0.592', '0.1217', '-0.311', '-0.1663', '0.08636', '0.1752', '-0.07184', '0.1371', '0.1237', '-0.02553', '0.126', '0.2925', '-0.12317', '0.3716', '-0.2024', '0.02834', '-0.829', '0.2812', '0.3728', '-0.3157', '-0.1421', '0.3457', '-0.03583', '0.3481', '0.06024', '-0.2494', '0.04318', '0.1552', '0.2708', '-0.284', '0.03302', '-0.2852', '-0.2715', '0.3035', '-0.2205', '0.494', '0.12225', '-0.1447', '-0.11755', '-0.1661', '-0.1802', '0.3877', '0.3164', '-0.01155', '0.2463', '-0.4265', '0.12396', '0.0605', '-0.2605', '0.1388', '0.0317', '0.1364', '0.04355', '0.10626', '0.3696', '0.4424', '0.2144', '0.281', '-0.1648', '-0.2081', '0.1318']",,,,,,,
mondo:0016109,autosomal recessive distal myopathy,"['distal myopathy, autosomal recessive']",,,206653,CN229019,"['0.2866', '-0.1195', '-0.136', '0.0708', '-0.2328', '-0.4175', '0.0933', '0.1556', '-0.7856', '-0.358', '-0.08844', '-0.11896', '-0.2737', '0.822', '0.4233', '-0.2017', '-0.3428', '0.0453', '-0.0652', '-0.516', '-0.328', '0.1848', '-0.013405', '0.4155', '0.0852', '-0.6177', '-0.1031', '-0.3926', '-0.2761', '-0.003172', '0.4268', '-0.3882', '0.599', '0.1089', '0.2512', '0.02362', '-0.596', '-0.1992', '0.4155', '0.06433', '-0.3408', '-0.3762', '-0.178', '0.509', '0.3015', '-0.1448', '-0.1906', '0.2439', '0.02368', '0.05557', '0.1214', '-0.3289', '0.3472', '-0.10876', '0.2349', '0.01333', '-0.0705', '0.4197', '-0.1747', '-0.0502', '0.1355', '-0.3435', '0.2983', '0.2477', '-0.389', '0.2788', '0.1185', '0.4243', '-0.2876', '0.2942', '-0.1898', '-0.2112', '0.11127', '-0.5024', '0.8955', '0.5425', '-0.3496', '-0.2325', '-0.302', '-0.1605', '-0.01863', '-0.2118', '-0.05798', '0.1206', '-0.1525', '0.1442', '0.0965', '-0.182', '0.3616', '0.4004', '0.1301', '-0.1152', '-0.1273', '0.3274', '0.2148', '0.631', '0.31', '-0.2194', '0.0866', '-0.1992']",,,,,,,
mondo:0016112,hereditary inclusion-body myopathy,"['cytoplasmic body myopathy', 'inclusion myopathy']",,,206662,,,,,,,,,
mondo:0016113,bulbospinal muscular atrophy,"['spinal and bulbal muscular atrophy', 'spinal-bulbar muscular atrophy', 'SBMA', 'bulbospinal muscular atrophy']",,,206701,,,,,,,,,
mondo:0016114,bulbospinal muscular atrophy of childhood,"['pediatric bulbospinal muscular atrophy', 'bulbospinal muscular atrophy of childhood', 'childhood bulbospinal muscular atrophy', 'paediatric bulbospinal muscular atrophy']",,,206704,,,,,,,,,
mondo:0016115,bulbospinal muscular atrophy of adulthood,"['bulbospinal muscular atrophy of adult', 'bulbospinal muscular atrophy of adults', 'adult bulbospinal muscular atrophy']",,,206707,,,,,,,,,
mondo:0016116,generalized bulbospinal muscular atrophy,,,,206710,,,,,,,,,
mondo:0016120,myotonic syndrome,,,,206970,,,,,D020967,,,10028658,
mondo:0016121,congenital myotonia,,,,206973,,,,,,,,,
mondo:0016122,periodic paralysis,"['periodic paralysis (disease)', 'periodic paralysis']",,,206976,CN231077,,,,D010245,,,10016208,0003768
mondo:0016125,"infectious, fungal or parasitic myopathy",,,,206988,,,,,,,,,
mondo:0016126,viral myositis,,,,206991,C0150005,,,,,729.1,,10051512,
mondo:0016127,bacterial myositis,,,,206994,,,,,,,,,
mondo:0016128,parasitic myositis,,,,206997,C0263997,,,,,728.2,,,
mondo:0016129,eosinophilic gastroenteritis,"['eosinophilic enteritis', 'eosinophilic gastroenteritis', 'EGE', 'eosinophilic gastroenterocolitis']",4031,,2070,C1262481,,C35330,,,558.41,,10017902,
mondo:0016130,fungal myositis,,,,207000,C0410251,,,,,,,,
mondo:0016139,qualitative or quantitative protein defects in neuromuscular diseases,,,,207049,CN200901,,,,,,,,
mondo:0016140,sarcoglycanopathy,['qualitative or quantitative defects of sarcoglycan'],,,207052,,,,,D058088,,,,
mondo:0016141,qualitative or quantitative defects of alpha-sarcoglycan,['alpha-sarcoglycanopathy'],,,207060,,,,,,,,,
mondo:0016142,qualitative or quantitative defects of beta-sarcoglycan,['beta-sarcoglycanopathy'],,,207063,C2930900,,,,C535435,,,,
mondo:0016143,qualitative or quantitative defects of gamma-sarcoglycan,['gamma-sarcoglycanopathy'],,,207067,,,,,,,,,
mondo:0016144,qualitative or quantitative defects of delta-sarcoglycan,['delta-sarcoglycanopathy'],,,207070,CN072428,,,,,,,,
mondo:0016145,qualitative or quantitative defects of dysferlin,['dysferlinopathy'],,,207073,C2931687,,,,C537995,,,,
mondo:0016146,caveolinopathy,['qualitative or quantitative defects of caveolin-3'],,,207078,CN043575,,,,,,,,
mondo:0016147,qualitative or quantitative defects of dystrophin,['dystrophinopathy'],,,207085,CN043595,,,,,,,,
mondo:0016149,qualitative or quantitative defects of merosin,,,,207094,,,,,,,,,
mondo:0016150,qualitative or quantitative defects of integrin alpha-7,['integrinopathy'],,,207098,,,,,,,,,
mondo:0016151,qualitative or quantitative defects of perlecan,,,,207101,,,,,,,,,
mondo:0016152,qualitative or quantitative defects of calpain,,,,207104,,,,,,,,,
mondo:0016153,qualitative or quantitative defects of TRIM32,,,,207107,,,,,,,,,
mondo:0016154,qualitative or quantitative defects of myotubularin,,,,207110,,,,,,,,,
mondo:0016155,qualitative or quantitative defects of protein involved in O-glycosylation of alpha-dystroglycan,"['secondary dystroglycanopathy', 'secondary alpha-dystroglycanopathy']",,,207113,,,,,,,,,
mondo:0016156,qualitative or quantitative defects of FKRP,,,,207119,,,,,,,,,
mondo:0016157,qualitative or quantitative defects of fukutin,,,,207122,,,,,,,,,
mondo:0016158,narcolepsy-cataplexy syndrome,"['narcoleptic syndrome', 'paroxysmal sleep', 'narcolepsy with cataplexy', 'narcolepsy-cataplexy syndrome', 'Gélineau disease', 'GC)lineau disease', 'Gelineau syndrome', 'Gelineau^s syndrome']",,,2073,,"['0.2122', '0.771', '-0.5293', '0.5645', '-0.5596', '-0.633', '0.7197', '0.584', '0.06964', '-0.2878', '0.013', '0.06696', '-0.2451', '0.371', '-0.2382', '-0.4326', '-0.0929', '-0.10626', '-0.1422', '-0.859', '0.01451', '0.3613', '0.1941', '-0.08167', '0.09753', '-0.766', '0.3875', '-0.1295', '0.06116', '0.3174', '0.1705', '0.07806', '0.33', '0.198', '-0.278', '0.0761', '-0.5244', '-0.2869', '0.457', '-0.5073', '1.112', '0.1545', '-0.3784', '0.12463', '0.2357', '-0.1669', '-0.4612', '0.00346', '0.08954', '1.011', '-0.116', '0.02031', '-0.1377', '-0.4946', '0.59', '0.03738', '0.2401', '-0.2893', '0.05548', '-0.4094', '-0.088', '0.1846', '-0.001371', '-0.1354', '-0.92', '0.5566', '0.1895', '-0.05267', '-0.2184', '0.924', '-0.6665', '0.448', '-0.131', '-0.4126', '0.533', '0.59', '-0.3928', '0.7036', '-0.1464', '0.08', '0.427', '-0.6074', '0.273', '-0.1293', '4.506e-05', '-0.10315', '0.06055', '0.725', '0.9097', '0.837', '0.1709', '-0.1698', '-0.442', '0.1521', '-0.09625', '0.3325', '-0.488', '-0.871', '-0.4402', '-0.2223']",,0000614,,347.0,G47.419,10028713,
mondo:0016159,Gemignani syndrome,"['spinocerebellar ataxia-amyotrophy-deafness syndrome', 'spinocerebellar ataxia associated amyotrophy of the hands and sensorineural deafness']",,,2074,C2931587,,,,C537678,,,,
mondo:0016160,X-linked intellectual disability-epilepsy syndrome,,,,2076,CN226857,"['1.096', '0.1659', '-0.2462', '0.0439', '-0.386', '-0.3787', '0.8833', '0.3015', '-0.611', '-0.4119', '0.22', '-0.321', '-0.6084', '0.5376', '-0.013596', '0.0528', '-0.3958', '-0.412', '-0.7573', '-0.885', '-0.313', '0.793', '0.0654', '-0.623', '-0.1813', '-0.0867', '-0.001869', '-0.01023', '-0.4492', '0.4563', '0.2722', '-0.726', '0.284', '0.182', '0.9165', '0.4868', '-0.1824', '0.08875', '-0.0099', '-0.528', '-0.259', '-0.56', '0.0644', '-0.2104', '-0.5283', '-0.8955', '-0.187', '0.3704', '0.564', '0.62', '-0.406', '0.3066', '0.06192', '-0.495', '0.01051', '-0.06854', '-0.1271', '0.00928', '-0.0782', '0.4106', '-1.115', '0.8115', '0.7075', '-0.3171', '-0.4734', '1.609', '0.2499', '-0.014435', '-1.247', '0.6646', '1.167', '1.086', '-0.115', '-0.52', '0.318', '0.8237', '1.085', '0.658', '-0.4912', '0.488', '-0.199', '0.873', '0.3667', '0.4573', '0.4492', '0.3384', '0.2428', '0.6973', '0.863', '0.4614', '-0.1455', '-0.0333', '-0.1631', '0.2205', '0.1825', '0.2424', '0.275', '-0.8086', '0.2477', '0.303']",,,,,,,
mondo:0016161,cerebral gigantism-jaw cysts syndrome,"['Cramer Niederdellmann syndrome', 'Cramer-Niederdellmann syndrome', 'cerebral gigantism jaw cysts']",,,2081,CN200907,,,,,,,,
mondo:0016162,bilateral frontal polymicrogyria,,0080921,,208444,,"['-0.1204', '0.3352', '0.3428', '-0.11456', '0.06287', '-0.278', '-0.1641', '-0.08167', '-0.7827', '0.07336', '-0.3535', '-0.3977', '0.07294', '0.04156', '0.1746', '0.2313', '-0.2988', '-0.619', '-0.17', '-0.38', '-0.0679', '0.09174', '0.03888', '0.04733', '0.3218', '-0.0091', '0.02415', '0.08276', '-0.2438', '0.2074', '0.0833', '-0.02376', '0.05', '-0.3499', '0.307', '-0.03293', '-0.505', '0.02785', '0.0012', '-0.1891', '0.494', '-0.493', '-0.2062', '0.0815', '0.4854', '0.185', '-0.06073', '0.0934', '-0.149', '-0.0782', '0.1326', '-0.3206', '-0.3047', '-0.01633', '-0.2297', '0.0586', '0.2228', '0.2354', '-0.373', '0.4084', '-0.3037', '-0.2311', '0.279', '0.2194', '-0.583', '0.253', '0.1859', '0.2228', '-0.313', '0.3154', '-0.04092', '0.3455', '0.5117', '-0.2522', '0.2107', '0.692', '0.2252', '-0.004333', '-0.2126', '-0.3167', '0.06323', '-0.2267', '-0.01933', '0.1306', '0.05374', '-0.346', '-0.259', '0.4246', '0.3755', '0.5312', '-0.2417', '0.4421', '0.182', '-0.1975', '0.6763', '0.039', '0.2278', '-0.12213', '0.2152', '-0.003132']",,,,,,,
mondo:0016163,autosomal dominant cerebellar ataxia type II,"['Adca, type 2', 'olivopontocerebellar atrophy 3', 'spinocerebellar ataxia type 7', 'ATXN7 autosomal dominant cerebellar ataxia type II', 'OPCA with retinal Degeneration', 'ADCA2', 'ADCA, type II', 'autosomal dominant cerebellar ataxia type II', 'autosomal dominant cerebellar ataxia type II caused by mutation in ATXN7', 'OPCA with macular Degeneration and external ophthalmoplegia', 'SCA7', 'autosomal dominant cerebellar ataxia, type 2', 'cerebellar syndrome-pigmentary maculopathy syndrome', 'ataxia with pigmentary retinopathy', 'ADCAII', 'OPCA 3', 'autosomal dominant cerebellar ataxia type 2', 'OPCA III', 'spinocerebellar ataxia 7', 'OPCA3']",0050958,164500,94147,CN229031,"['0.0082', '-0.156', '-0.2922', '0.2167', '0.0421', '-0.4602', '0.1914', '0.537', '-0.649', '-0.729', '-0.0163', '-0.1115', '-0.1465', '0.5186', '0.383', '-0.3599', '-0.3647', '-0.1438', '0.3413', '-0.522', '-0.1494', '-0.3079', '0.1815', '-0.2119', '-0.05786', '-0.473', '-0.2484', '-0.02188', '-0.04626', '-0.6274', '0.2554', '0.1663', '-0.4614', '-0.2494', '0.2805', '0.274', '0.000349', '0.149', '0.3267', '0.3748', '0.4624', '0.03625', '-0.269', '0.4053', '0.3994', '-0.6426', '0.011215', '-0.09717', '0.1469', '0.07263', '0.02153', '-0.12494', '0.3303', '-0.575', '0.03134', '-0.501', '0.638', '0.3384', '-0.1863', '0.1432', '-0.3406', '0.1936', '0.0986', '0.08746', '-0.2793', '0.359', '0.3394', '0.2181', '-0.4888', '0.3372', '0.4688', '0.1926', '-0.03745', '-0.6724', '0.846', '0.0532', '0.1704', '-0.2092', '-0.0462', '0.2238', '0.01256', '-0.8213', '0.4338', '0.723', '-0.1824', '-0.5205', '0.1293', '-0.1321', '0.5537', '0.3308', '0.2966', '0.4285', '-0.1671', '0.00861', '0.508', '0.7437', '0.273', '0.523', '-0.01903', '-0.077']",C126562,,,,,,
mondo:0016164,herpetiform pemphigus,,,,208524,CN226858,,,,,,,,
mondo:0016165,hereditary hypoparathyroidism,['genetic hypoparathyroidism'],,,208593,,,,,,,,,
mondo:0016166,hereditary hyperparathyroidism,['genetic hyperparathyroidism'],,,208596,,,,,,,,,
mondo:0016167,optic pathway glioma,"['glioma of visual pathway', 'optic pathway glioma', 'glioma of the optic tract', 'glioma of optic tract', 'visual pathway glioma', 'optic tract glioma', 'glioma of the visual pathway']",,,2086,C0796418,,C8567,,,,,,
mondo:0016168,cryopyrin-associated periodic syndrome,"['Cryopyrinopathy', 'caps']",,,208650,C2316212,,C84657,,D056587,759.89,,10068850,
mondo:0016169,chronic acquired demyelinating polyneuropathy,"['chronic acquired peripheral neuropathy', 'acquired peripheral neuropathy, chronic', 'CADP']",,,208974,,,,,,,,,
mondo:0016170,chronic polyradiculoneuropathy,"['polyradiculoneuropathy, chronic']",,,208978,,,,,,,,,
mondo:0016171,polyradiculoneuropathy associated with IgG/IgA/IgM monoclonal gammopathy without known antibodies,,,,208981,,,,,,,,,
mondo:0016172,acquired sensory ganglionopathy,"['acquired sensory ganglionopathy', 'acquired sensory neuronopathy']",,,208984,,,,,,,,,
mondo:0016173,non-paraneoplastic sensory ganglionopathy,['non-paraneoplastic sensory neuronopathy'],,,208989,,,,,,,,,
mondo:0016174,paraneoplastic sensory ganglionopathy,['paraneoplastic sensory neuronopathy'],,,208999,,,,,,,,,
mondo:0016175,cutis laxa,"['loose skin', 'generalised elastolysis', 'elastolysis', 'generalized elastolysis', 'cutis laxa']",3144,,209,C0010495,,C84663,,D003483,,,10011692,
mondo:0016176,axonal polyneuropathy associated with IgG/IgM/IgA monoclonal gammopathy,,,,209004,,,,,,,,,
mondo:0016179,acquired amyloid peripheral neuropathy,,,,209013,,,,,,,,,
mondo:0016182,"qualitative or quantitative defects of protein O-mannose beta1, 2N-acetylglucosaminyltransferase",['qualitative or quantitative defects of protein POMGNT1'],,,209024,,,,,,,,,
mondo:0016183,qualitative or quantitative defects of protein glycosyltransferase-like,,,,209027,,,,,,,,,
mondo:0016184,qualitative or quantitative defects of protein O-mannosyltransferase 1,['qualitative or quantitative defects of protein O-mannosyltransferase type 1'],,,209030,,,,,,,,,
mondo:0016185,qualitative or quantitative defects of protein O-mannosyltransferase 2,['qualitative or quantitative defects of protein O-mannosyltransferase type 2'],,,209033,,,,,,,,,
mondo:0016186,qualitative or quantitative defects of myofibrillar proteins,,,,209038,,,,,,,,,
mondo:0016187,qualitative or quantitative defects of desmin,,,,209041,,,,,,,,,
mondo:0016188,qualitative or quantitative defects of alphaB-cristallin,,,,209044,,,,,,,,,
mondo:0016189,qualitative or quantitative defects of filamin C,['qualitative or quantitative defects of filamin type C'],,,209047,,,,,,,,,
mondo:0016190,qualitative or quantitative defects of protein ZASP,,,,209050,,,,,,,,,
mondo:0016191,qualitative or quantitative defects of titin,,,,209053,,,,,,,,,
mondo:0016192,qualitative or quantitative defects of telethonin,,,,209056,,,,,,,,,
mondo:0016193,qualitative or quantitative defects of alpha-actin,,,,209059,,,,,,,,,
mondo:0016194,qualitative or quantitative defects of nebulin,,,,209182,,,,,,,,,
mondo:0016195,qualitative or quantitative defects of beta-myosin heavy chain (MYH7),,,,209185,,,,,,,,,
mondo:0016196,qualitative or quantitative defects of emerin,,,,209188,,,,,,,,,
mondo:0016197,qualitative or quantitative defects of selenoprotein N1,,,,209193,,,,,,,,,
mondo:0016198,qualitative or quantitative defects of plectin,,,,209196,,,,,,,,,
mondo:0016199,qualitative or quantitative defects of protein SERCA1,,,,209199,,,,,,,,,
mondo:0016200,qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase,['qualitative or quantitative defects of glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase type -'],,,209203,,,,,,,,,
mondo:0016201,qualitative or quantitative defects of myotilin,,,,209224,,,,,,,,,
mondo:0016202,autosomal dominant rhegmatogenous retinal detachment,"['DRRD', 'rhegmatogenous retinal detachment, autosomal dominant']",,,209867,C1836081,"['-0.1567', '-0.4958', '-0.2299', '0.4438', '0.01464', '0.02576', '-0.322', '0.2489', '-0.3237', '-0.1769', '-0.1007', '-0.4692', '-0.4353', '0.689', '-0.1617', '-0.286', '-0.4692', '0.2712', '0.378', '-0.8003', '-0.438', '0.657', '-0.1494', '-0.002928', '-0.1143', '0.416', '-0.82', '0.5933', '0.4448', '0.689', '0.5596', '-0.2568', '0.2303', '0.126', '0.141', '0.6753', '-0.355', '-0.2233', '0.1213', '-0.9707', '0.3328', '0.10767', '-0.1213', '0.1726', '0.215', '0.1171', '-0.1477', '-0.513', '0.799', '0.2354', '0.5547', '0.2448', '0.2488', '-0.6196', '0.0807', '-0.37', '-0.05743', '0.2686', '-0.725', '-0.1844', '0.3723', '-0.07446', '-0.03534', '0.1858', '-0.1945', '-0.06015', '0.653', '0.675', '-0.4978', '0.9526', '0.04916', '0.3855', '0.104', '-0.9473', '0.02742', '-0.02213', '0.1909', '0.785', '-0.4844', '0.3682', '-0.2983', '-0.526', '-0.5884', '0.581', '-0.217', '-0.7773', '0.554', '0.6084', '0.568', '0.3398', '-0.3262', '0.423', '-0.2046', '0.1272', '0.6587', '-0.5195', '0.00887', '-0.5103', '-0.4778', '0.4832']",,,,,,,
mondo:0016203,hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency,,,,209902,,,,,,,,,
mondo:0016204,idiopathic copper-associated cirrhosis,['non-Wilsonian hepatic copper toxicosis of infancy and childhood'],,,209919,,,,,,,,,
mondo:0016205,IRVAN syndrome,"['idiopathic retinal-aneurysms-neuroretinitis syndrome', 'idiopathic retinal vasculitis-aneurysms-neuroretinitis syndrome']",,,209943,C3665812,,,,,,,,
mondo:0016206,idiopathic uveal effusion syndrome,,,,209956,CN200962,,,,,,,,
mondo:0016207,phacoanaphylactic uveitis,"['Phacoallergic endophthalmitis', 'Phacoantigenic endophthalmitis', 'Phako-anaphylactic endophthalmitis', 'endophthalmitis phacoanaphylactica', 'lens-induced iridocyclitis', 'lens-induced uveitis', 'lens-induced endophthalmitis']",,,209959,C1444621,,,,,,,,
mondo:0016208,solitary rectal ulcer syndrome,,,,209964,CN200964,,,,,,K62.6,,
mondo:0016209,benign familial nocturnal alternating hemiplegia of childhood,"['benign nocturnal alternating hemiplegia of childhood', 'benign familial nocturnal alternating hemiplegia in childhood']",,,209973,CN226880,,,,,,,,
mondo:0016210,alternating hemiplegia,,,,209978,,,,,,,,,
mondo:0016211,non-papillary transitional cell carcinoma of the bladder,['non-papillary urothelial carcinoma'],,,209989,CN200968,,,,,,,,
mondo:0016213,leukonychia totalis-acanthosis-nigricans-like lesions-abnormal hair syndrome,,,,210133,CN226881,,,,,,,,
mondo:0016214,pulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndrome,,,,210136,CN200975,,,,,,,,
mondo:0016215,spastic quadriplegic cerebral palsy,"['spastic quadriplegic cerebral palsy', 'quadriplegic infantile cerebral palsy', 'inherited congenital spastic tetraplegia', 'spastic tetraplegia cerebral palsy', 'inherited congenital spastic quadriplegia', 'spastic quadriplegia', 'tetraplegic infantile cerebral palsy']",10970,,210141,C0154697,"['-0.06744', '0.0692', '0.0693', '-0.3608', '0.08954', '-0.4983', '-0.1454', '-0.03488', '-0.4478', '-0.3616', '-0.0592', '-0.3245', '-0.12006', '-0.3032', '0.10486', '-0.0876', '-0.1252', '-0.2122', '-0.2693', '-0.7393', '0.2218', '0.1337', '0.0669', '-0.2186', '-0.01752', '-0.1464', '0.07947', '0.2058', '0.131', '-0.2913', '0.412', '0.0829', '0.5107', '0.2206', '-0.2091', '0.1326', '-0.3613', '-0.254', '-0.2249', '-0.162', '0.1707', '-0.014084', '-0.2285', '0.1848', '-0.0809', '-0.163', '0.0346', '0.217', '-0.0543', '0.076', '-0.1512', '-0.04385', '-0.2693', '-0.3784', '0.0496', '-0.3042', '0.2556', '0.0803', '-0.07623', '0.291', '-0.04977', '-0.0908', '0.704', '0.1737', '-0.6597', '0.2905', '0.4485', '0.4824', '-0.843', '0.4822', '-0.08154', '0.4229', '0.005287', '-0.2085', '0.1637', '-0.1199', '0.4226', '-0.02216', '-0.1493', '-0.1588', '-0.03818', '0.0793', '0.3423', '0.5215', '-0.01145', '-0.02124', '-0.1492', '0.2341', '0.2092', '0.07196', '0.2974', '0.3792', '0.1997', '0.05615', '0.2185', '0.399', '0.536', '0.2029', '0.4814', '0.02809']",C116904,,,344.09,G11.4,,
mondo:0016216,adult hepatocellular carcinoma,"['adult primary carcinoma of liver cell', 'adult primary hepatoma', 'adult HCC', 'hepatocellular carcinoma of adults', 'adult primary carcinoma of the liver cell', 'hepatocellular cancer', 'adult primary liver cell carcinoma', 'adult hepatocellular carcinoma', 'adult hepatoma', 'adult primary hepatocellular carcinoma']",0070328,,210159,CN200978,,C7956,,,,,,
mondo:0016217,mal de Debarquement,"['sickness of disembarkment', 'Mal de debarquement syndrome', 'disembarkment syndrome', 'MDD', 'Mal de débarquement', 'MdDS']",,,210272,C1608983,,,,C537840,,,10064924,
mondo:0016218,Guillain-Barre syndrome,"['post-infective polyneuritis', 'acute inflammatory neuropathy', 'Guillain-Barré-Strohl syndrome', 'acute postinfectious polyneuropathy', 'GBS', 'post-infectious polyneuritis', 'Guillain-Barré syndrome', 'acute autoimmune peripheral neuropathy', 'Landry^s ascending paralysis', 'Landry-Guillain-Barre-Strohl syndrome', 'Guillain Barré syndrome', 'Guillain Barre syndrome', 'acute immune-mediated polyneuropathy', 'postinfectious polyneuritis', 'Guillain-Barre-Strohl syndrome', 'acute inflammatory demyelinating polyneuropathy']",12842,,2103,C0018378,,C116345,0007292,D020275,,G61.0,10018767,
mondo:0016219,dysmorphism-pectus carinatum-joint laxity syndrome,"['Guizar Vasquez Sanchez Manzano syndrome', 'dysmorphism-pectus carinatum-joint laxity syndrome', 'Guízar Vázquez-Sánchez-Manzano syndrome']",,,2104,CN237430,,,,,,,,
mondo:0016220,congenital temporomandibular joint ankylosis,['congenital trismus'],,,210576,,,,,,,,,
mondo:0016221,temporomandibular joint anomaly,,,,210581,,,,,,,,,
mondo:0016222,spindle cell hemangioma,"['spindle -cell hemangioma', 'SCh', 'spindle cell hemangioma', 'spindle cell hemangioendothelioma']",496,,210584,C1304508,,C4754,0002856,,,,,
mondo:0016223,infantile hemangioma of rare localization,,,,210589,CN226884,,,,,,,,
mondo:0016224,autosomal dominant proximal spinal muscular atrophy,"['proximal spinal muscular atrophy, autosomal dominant']",,,211037,CN229044,,,,,,,,
mondo:0016225,specific learning disability,"['specific learning disorder', 'specific learning difficulty']",,,211047,CN226885,,,,D000067559,,,,
mondo:0016226,specific language disorder,['dysphasia'],,,211053,CN200992,,,,D000080888,,,,
mondo:0016227,hereditary episodic ataxia,"['Isaacs syndrome', 'episodic ataxia syndrome', 'ea syndrome', 'episodic ataxia']",963,,211062,C1720189,,,1000638,,,,,
mondo:0016229,hereditary vascular anomaly,['genetic vascular anomaly'],,,211240,,,,,,,,,
mondo:0016230,simple vascular malformation,,,,211243,,,,,,,,,
mondo:0016231,capillary malformation,['rare capillary malformation'],,,211247,,,,,,,,,
mondo:0016236,kaposiform hemangioendothelioma,"['congenital cutaneous multifocal kaposiform hemangioendothelioma', 'Kaposiform hemangio-endothelioma', 'KH', 'KHE', 'Kaposiform hemangioendothelioma']",,,2122,C1367420,,C27510,,C537007,,,,
mondo:0016237,diffuse neonatal hemangiomatosis,,,,2123,C0474965,,,,,,,,
mondo:0016238,solitary fibrous tumor,"['SFT', 'submesothelial fibroma', 'localised fibrous mesothelioma', 'solitary fibrous tumor', 'localized fibrous tumor', 'localised fibrous tumour', 'hemangiopericytoma', 'localized fibrous mesothelioma', 'solitary fibrous tumor/hemangiopericytoma']",,,2126,C1266119,,C7634,,D054364,238.1,,10018825,
mondo:0016239,cystinosis,"['Cystinoses', 'cystine storage disease', 'cystine disease', 'cystine diathesis', 'Protein defect of cystin transport']",1064,,213,CN035091,"['-0.04507', '-0.02988', '0.1554', '0.1194', '0.2546', '-0.4685', '-0.7666', '0.4512', '-0.2764', '0.1004', '-0.7153', '0.1404', '-0.1729', '0.914', '-0.4446', '-0.5654', '0.1', '-0.0724', '0.02625', '-0.383', '-0.1133', '-0.1743', '0.9395', '-0.246', '0.10815', '-0.5996', '-0.1722', '0.3772', '-0.8706', '0.368', '0.638', '-0.02568', '0.1926', '-0.2803', '0.1366', '0.5063', '-0.2502', '-0.05124', '-0.3315', '0.8853', '-0.06116', '-0.765', '0.2542', '-0.2004', '0.2449', '0.04175', '0.0793', '0.02837', '-0.299', '-0.02527', '-0.576', '0.4456', '0.273', '-0.3093', '-0.2467', '-0.528', '0.5015', '0.3445', '-0.472', '-0.05463', '-0.0505', '-0.207', '-0.3936', '-0.232', '0.2844', '-0.7344', '0.6533', '0.1384', '-0.435', '-0.4724', '-0.0823', '-0.2134', '0.2106', '-0.304', '0.2155', '0.3022', '0.4556', '-0.1143', '0.06696', '0.572', '0.01633', '-0.316', '-0.02226', '0.4585', '-0.3662', '-0.257', '-0.03195', '-0.3835', '0.897', '0.1617', '0.3809', '0.2263', '-0.2776', '-0.7344', '0.3633', '0.1624', '0.3281', '-0.4229', '-0.377', '-0.1643']",C2976,,D003554,,E72.04,10011777,
mondo:0016240,hemimelia,['longitudinal meromelia'],,,498491,C0018987,,C34674,,,,,10019464,
mondo:0016241,alternating hemiplegia of childhood,"['childhood alternating hemiplegia', 'alternating hemiplegia syndrome', 'congenital adrenal gland hypoplasia', 'paediatric alternating hemiplegia', 'pediatric alternating hemiplegia', 'adrenal hypoplasia congenita', 'alternating hemiplegia', 'congenital adrenal Hypoplasia', 'alternating hemiplegia of childhood', 'AHC']",0050635,,2131,C0338488,"['0.0965', '0.10474', '-0.4875', '-0.2817', '-0.0326', '-0.276', '0.4722', '0.2898', '-0.2664', '0.003046', '-0.3281', '0.397', '-0.1832', '0.02571', '0.1656', '0.3315', '-0.0812', '-0.2063', '-0.1322', '-0.681', '0.01608', '0.0284', '-0.04745', '-0.6646', '-0.482', '-0.3608', '-0.1155', '0.0459', '-0.0663', '-0.579', '0.2974', '-0.01344', '0.3833', '0.563', '-0.1844', '0.1919', '-0.5225', '-0.36', '-0.2048', '-0.0881', '0.8965', '-0.02711', '-0.0777', '-0.288', '0.6904', '-0.1974', '0.0718', '0.1831', '-0.2515', '0.9243', '-0.3672', '0.2433', '-0.1351', '-0.5483', '0.2976', '0.7334', '0.449', '-0.1677', '-0.0479', '-0.0824', '-0.096', '0.498', '0.488', '-0.1698', '-0.6216', '0.08575', '0.431', '0.4807', '0.407', '0.3643', '-0.4072', '0.2607', '-0.05334', '-0.1438', '0.2761', '0.2117', '0.4465', '-0.1404', '-0.2417', '-0.09906', '0.1927', '-0.2625', '0.1715', '0.4985', '0.3267', '0.153', '0.263', '0.555', '-0.1288', '0.537', '0.5405', '0.2517', '0.0718', '0.1816', '0.2245', '0.1893', '0.2238', '-0.3174', '0.0977', '0.3']",C35261,,C536589,,,,
mondo:0016242,hemoglobin C disease,"['Hb-C disease', 'Hb C disease']",2859,,2132,C0019021,,C34675,,D006445,282.7,,10018883,
mondo:0016243,hemoglobin E disease,"['Hb-E disease', 'hemoglobin E disease']",5379,,2133,C0238159,,C35287,,,282.7,,10053215,
mondo:0016244,atypical hemolytic-uremic syndrome,"['hemolytic-uremic syndrome without diarrhea', 'HUS, atypical', 'non-diarrhea-associated hemolytic uremic syndrome', 'atypical HUS', 'atypical hemolytic uremic syndrome', 'hemolytic-uremic syndrome without diarrhoea', 'D-minus hemolytic uremic syndrome (D-HUS)', 'D-HUS', 'aHUS']",0080301,,2134,C2931788,"['-0.385', '0.2231', '-0.1534', '-0.07245', '-0.113', '-0.2869', '-0.233', '-0.0552', '0.226', '0.1304', '0.177', '-0.3037', '0.158', '-0.05386', '-0.06964', '-0.4502', '-0.0556', '-0.1316', '0.2069', '-0.72', '0.2578', '-0.3384', '0.513', '-0.04666', '0.231', '-0.0725', '0.1536', '0.01149', '0.3071', '-0.356', '-0.10004', '0.1114', '0.4346', '0.482', '0.08746', '-0.615', '-0.3987', '-0.01098', '-0.11584', '-0.2856', '-0.4827', '-0.1356', '0.2019', '-0.05286', '0.1615', '-0.4028', '-0.2795', '-0.1635', '0.11206', '0.2522', '-0.2496', '0.2747', '0.1385', '0.02203', '-0.3125', '-0.1614', '0.413', '-0.1398', '-0.4934', '0.17', '0.4692', '-0.003819', '0.3623', '-0.2083', '0.2489', '-0.2467', '0.383', '0.2817', '-0.2216', '0.5205', '-0.2864', '-0.299', '0.00272', '0.11725', '0.0625', '-0.2993', '0.281', '0.1214', '-0.07886', '0.10266', '-0.1802', '-0.2386', '0.0949', '-0.03647', '-0.2306', '-0.1815', '0.1078', '0.3997', '0.05295', '-0.3687', '0.4783', '0.00946', '0.09576', '-0.0734', '0.2986', '0.4324', '0.3826', '-0.3838', '-0.1998', '0.368']",C123223,,D065766,,,,
mondo:0016248,familial ovarian cancer,"['familial ovarian malignant tumour', 'familial ovarian malignant tumor', 'hereditary ovarian cancer']",,,213517,CN201036,,,,,,,,
mondo:0016249,hereditary site-specific ovarian cancer syndrome,,,,213524,CN201037,,,,,,,,
mondo:0016255,uterine corpus mixed epithelial and mesenchymal neoplasm,"['body of uterus mixed neoplasm', 'uterine corpus mixed epithelial and mesenchymal tumor', 'malignant mixed epithelial and mesenchymal tumour of corpus uteri', 'malignant mixed epithelial and mesenchymal tumor of corpus uteri', 'mixed epithelial and mesenchymal cancer of corpus uteri', 'uterine corpus mixed epithelial and mesenchymal neoplasm', 'uterine corpus mixed epithelial and mesenchymal tumour']",,,213589,C1519858,,C40181,,,,,,
mondo:0016256,Hennekam syndrome,"['intestinal lymphagiectasia lymphedema intellectual deficit syndrome', 'lymphedema-lymphangiectasia-intellectual disability syndrome', 'Hennekam lymphangiectasia-lymphedema syndrome', 'lymphangiectasies and lymphedema Hennekam type', 'lymphedem-lymphangiectasia-intellectual disability syndrome', 'Hennekam lymphangiectasia lymphedema syndrome']",0060366,,2136,C0340834,"['0.1968', '0.06058', '-0.1476', '-0.3713', '-0.2773', '0.0804', '0.7456', '0.42', '-0.4016', '-0.5903', '0.04852', '-0.1357', '0.5337', '0.4087', '-0.5635', '0.1761', '0.2155', '-0.0406', '-0.5566', '-0.8105', '0.1617', '0.0825', '0.2578', '-0.3958', '0.2241', '-0.667', '-0.4602', '0.167', '0.4922', '-0.4663', '0.566', '-0.58', '-0.1687', '-0.09875', '-0.1011', '-0.321', '0.2334', '-0.5117', '0.01799', '0.1327', '-0.0824', '0.1375', '0.2915', '-0.1505', '0.287', '0.014824', '0.05472', '0.3816', '-0.4524', '0.1048', '-0.4456', '0.003452', '0.5967', '-0.3252', '-0.558', '-0.0308', '-0.03976', '-0.616', '-0.03445', '0.1786', '-0.3489', '-0.2903', '-0.0574', '-0.5093', '-0.03174', '-0.788', '0.307', '0.4321', '-0.3584', '0.02684', '-0.6436', '-0.1417', '0.03033', '-0.03702', '-0.4888', '0.1276', '0.4373', '-0.1846', '0.2969', '-0.3271', '-0.2323', '0.03072', '-0.2673', '0.4634', '0.1765', '-0.0398', '-0.4846', '-0.604', '0.3286', '0.0009103', '0.2927', '0.3103', '-0.3142', '0.05286', '0.738', '-0.00913', '-0.1385', '-0.8145', '0.6187', '0.1263']",,,,457.1,,,
mondo:0016258,uterine corpus carcinofibroma,"['uterine corpus Carcinofibroma', 'Carcinofibroma of the corpus uteri']",,,213605,C1883485,,C40182,,,,,,
mondo:0016259,carcinosarcoma of the corpus uteri,"['mixed Müllerian cancer of corpus uteri', 'malignant mixed Müllerian tumour of the corpus uteri', 'uterine corpus malignant mixed mesodermal (Müllerian) tumor', 'malignant mixed mesodermal tumor of the uterus', 'uterine corpus malignant mixed mesodermal (Müllerian) tumour', 'uterine malignant mixed mesodermal tumour', 'uterine mixed Müllerian sarcoma', 'uterine corpus malignant mixed mesodermal neoplasm', 'corpus uteri malignant mixed mesodermal tumour', 'malignant mixed mesodermal neoplasm of the uterus', 'malignant mixed Mullerian tumor of the corpus uteri', 'malignant mixed mesodermal tumor of the uterine corpus', 'malignant mixed mesodermal tumour of uterine body', 'mixed Müllerian sarcoma of the uterus', 'uterine body malignant mixed mesodermal tumour', 'uterine corpus malignant mixed Mullerian tumor', 'uterine body malignant mixed mesodermal tumor', 'carcinosarcoma of the uterine body', 'malignant mixed mesodermal neoplasm of the uterine corpus', 'malignant mixed Müllerian tumor of the corpus uteri', 'mixed Mullerian sarcoma of the uterus', 'carcinosarcoma of uterine body', 'corpus uteri malignant mixed mesodermal tumor', 'uterine body carcinosarcoma', 'uterine body malignant mixed mesodermal neoplasm', 'mixed Mullerian cancer of corpus uteri', 'uterine corpus malignant mixed Müllerian tumour', 'malignant mixed mesodermal neoplasm of uterine corpus', 'uterine corpus malignant mixed Mullerian tumour', 'uterine corpus malignant mixed Müllerian tumor', 'malignant mixed mesodermal neoplasm of uterus', 'malignant mixed mesodermal tumor of the uterine body', 'malignant mixed mesodermal tumour of uterine corpus', 'uterine corpus malignant mixed mesodermal tumor', 'malignant mixed müllerian tumor of corpus uteri', 'malignant mixed Mullerian tumour of the corpus uteri', 'uterine carcinosarcoma', 'body of uterus carcinosarcoma', 'malignant mixed mesodermal tumour of the uterine body', 'malignant mixed mesodermal tumor of uterine corpus', 'uterine mixed Mullerian sarcoma', 'uterine corpus carcinosarcoma', 'uterine malignant mixed mesodermal tumor', 'uterine corpus malignant mixed Mullerian neoplasm', 'uterine corpus malignant mixed mesodermal tumour', 'uterine corpus malignant mixed mesodermal (Mullerian) tumour', 'malignant mixed müllerian tumour of corpus uteri', 'mixed Mullerian sarcoma of uterus', 'malignant mixed mesodermal neoplasm of the uterine body', 'uterine corpus malignant mixed Müllerian neoplasm', 'malignant mixed mesodermal tumour of the uterus', 'malignant mixed mesodermal tumour of the uterine corpus', 'malignant mixed mesodermal neoplasm of uterine body', 'carcinosarcoma of corpus uteri', 'mixed Müllerian sarcoma of uterus', 'carcinosarcoma of uterine corpus', 'carcinosarcoma of the uterine corpus', 'uterine malignant mixed mesodermal neoplasm', 'carcinosarcoma of the uterus', 'carcinosarcoma of the corpus uteri', 'malignant mixed mesodermal tumor of uterine body', 'carcinosarcoma of uterus', 'malignant mixed mesodermal tumor of uterus', 'uterine corpus malignant mixed mesodermal (Mullerian) tumor', 'malignant mixed mesodermal tumour of uterus']",,,213610,,,C9180,,,,,,
mondo:0016260,uterine corpus rhabdomyosarcoma,"['uterine corpus rhabdomyosarcoma', 'body of uterus rhabdomyosarcoma (disease)', 'rhabdomyosarcoma of the corpus uteri']",,,213615,C4288047,,C127058,,,,,,
mondo:0016262,leiomyosarcoma of the corpus uteri,"['leiomyosarcoma of the body of uterus', 'leiomyosarcoma of the uterine corpus', 'leiomyosarcoma of the uterus', 'uterus leiomyosarcoma', 'body of uterus leiomyosarcoma', 'uterine leiomyosarcoma', 'uterine corpus leiomyosarcoma', 'leiomyosarcoma of uterus', 'leiomyosarcoma - uterus', 'leiomyosarcoma of corpus uteri', 'corpus uteri leiomyosarcoma', 'leiomyosarcoma of uterine body', 'uterine body leiomyosarcoma', 'leiomyosarcoma of body of uterus', 'leiomyosarcoma of the corpus uteri', 'leiomyosarcoma of the uterine body', 'leiomyosarcoma of uterine corpus']",5289,,213625,C0280631,,C6340,,,,,,
mondo:0016263,primitive neuroectodermal tumor of the corpus uteri,"['peripheral neuroectodermal cancer of the corpus uteri', 'body of uterus primitive neuroectodermal tumor', 'primitive neuroectodermal tumour of body of uterus', 'malignant peripheral neuroectodermal tumour of the corpus uteri', 'body of uterus primitive neuroectodermal tumour', 'malignant peripheral neuroectodermal tumor of the corpus uteri']",,,213630,CN201052,,,,,,,,
mondo:0016264,autoimmune hepatitis,"['AIH', 'autoimmune hepatitis', 'autoimmune liver disease', 'autoimmune chronic hepatitis', 'autoimmune chronic active hepatitis', 'chronic autoimmune hepatitis', 'autoimmune hepatitis with centrilobular necrosis']",2048,,2137,C1332355,,C27029,0005676,D019693,571.42,K75.4,10003827,
mondo:0016266,squamous cell carcinoma of the corpus uteri,"['body of uterus squamous cell carcinoma', 'endometrial squamous cell carcinoma']",,,213716,,,,,,,C50,,
mondo:0016267,undifferentiated carcinoma of the corpus uteri,"['endometrial undifferentiated carcinoma', 'body of uterus undifferentiated carcinoma']",,,213721,,,,,,,C50,,
mondo:0016268,papillary carcinoma of the corpus uteri,"['body of uterus papillary carcinoma', 'endometrial capillary carcinoma']",,,213726,CN201057,,,,,,,,
mondo:0016269,high-grade neuroendocrine carcinoma of the corpus uteri,"['poorly differentiated neuroendocrine carcinoma of the endometrium', 'high-grade neuroendocrine carcinoma of the uterine corpus', 'poorly differentiated neuroendocrine carcinoma of the corpus uteri']",,,213731,CN201058,,,,,,,,
mondo:0016270,low-grade neuroendocrine tumor of the corpus uteri,"['low-grade neuroendocrine tumor of the uterine corpus', 'well-differentiated neuroendocrine neoplasm of the endometrium', 'low-grade neuroendocrine tumour of the uterine corpus', 'well-differentiated neuroendocrine tumor of the endometrium', 'well-differentiated neuroendocrine tumour of the corpus uteri', 'well-differentiated neuroendocrine tumour of the endometrium', 'well-differentiated neuroendocrine tumor of the corpus uteri']",,,213736,CN201059,,,,,,,,
mondo:0016271,adenoid cystic carcinoma of the corpus uteri,"['endometrial adenoid cystic carcinoma', 'body of uterus adenoid cystic carcinoma']",,,213741,,,,,,,,,
mondo:0016272,transitional cell carcinoma of the corpus uteri,"['endometrial transitional cell carcinoma', 'body of uterus transitional cell carcinoma']",,,213746,,,,,,,,,
mondo:0016273,malignant germ cell tumor of corpus uteri,"['body of uterus malignant germ cell tumor', 'body of uterus malignant germ cell tumour', 'germ cell cancer of the corpus uteri', 'germ cell cancer of corpus uteri', 'malignant germ cell tumor of the corpus uteri', 'malignant germ cell tumour of the corpus uteri']",,,213751,CN201062,,,,,,,,
mondo:0016276,high-grade neuroendocrine carcinoma of the cervix uteri,"['poorly differentiated neuroendocrine cervical carcinoma', 'poorly differentiated neuroendocrine carcinoma of the cervix uteri', 'high-grade neuroendocrine carcinoma of the uterine cervix']",,,213777,CN201066,,,,,,C53.0,,
mondo:0016277,malignant mixed epithelial and mesenchymal tumor of cervix uteri,"['cervical malignant mixed epithelial and mesenchymal tumor', 'cervical malignant mixed epithelial and mesenchymal tumour', 'mixed epithelial and mesenchymal cancer of cervix uteri']",,,213782,CN201067,,,,,,C53.0,,
mondo:0016280,sarcoma of cervix uteri,"['malignant mesenchymal tumour of cervix uteri', 'cervical malignant mesenchymal tumor', 'uterine cervix sarcoma', 'cervical sarcoma', 'malignant mesenchymal tumor of cervix uteri', 'sarcoma of uterine cervix', 'cervical malignant mesenchymal tumour']",,,213797,CN201070,,,,,,C53.0,,
mondo:0016281,"46,XX ovotesticular disorder of sex development","['ovotesticular disorders of sex development', 'ovotesticular differences of sex development', 'true hermaphroditism', 'ovotesticular DSD', '46,XX ovotesticular DSD']",,,2138,CN776920,"['-0.01884', '-0.4128', '-0.1484', '-0.3481', '0.4268', '-0.369', '-0.06647', '0.698', '-0.6333', '-0.3015', '-0.0888', '-0.221', '0.06335', '0.6294', '-0.0707', '-0.05994', '0.1085', '0.4062', '-0.5693', '-0.5757', '-0.2201', '-0.06064', '1.212', '-0.818', '-0.1353', '-0.1882', '-0.0178', '0.494', '0.5127', '-0.4841', '0.7227', '0.07477', '0.7646', '-0.827', '-0.2505', '-0.01021', '-0.422', '-0.1862', '-0.1252', '0.3801', '0.65', '0.1584', '-0.0638', '-0.04556', '0.5293', '-0.2073', '-0.3398', '-0.2179', '0.3477', '0.6587', '0.05975', '-0.447', '-0.593', '0.2905', '-0.472', '0.2722', '0.3567', '-0.4214', '-0.747', '0.03546', '0.3047', '0.555', '0.2427', '0.3206', '-0.04102', '0.4028', '0.4346', '0.347', '-0.1007', '-0.2466', '0.02635', '0.0748', '-0.2502', '-0.4614', '0.4675', '-0.295', '0.08795', '0.3494', '-0.9043', '-0.856', '0.0707', '0.5303', '0.04828', '0.00766', '-0.1587', '-0.2157', '-0.1364', '-0.4585', '0.02852', '-0.668', '-0.3', '0.2576', '-0.4675', '-0.1509', '1.023', '-0.6655', '0.603', '-0.10925', '-0.0625', '0.0201']",C127167,,D050090,,,,
mondo:0016282,rhabdomyosarcoma of the cervix uteri,"['CERMS', 'cervical rhabdomyosarcoma', 'uterine cervix rhabdomyosarcoma (disease)']",,,213802,CN201072,,C128048,,,,C53.0,,
mondo:0016283,leiomyosarcoma of the cervix uteri,"['CELI', 'leiomyosarcoma of uterine cervix', 'cervical leiomyosarcoma', 'uterine cervix leiomyosarcoma']",,,213807,CN201073,,C128047,,,,C53.0,,
mondo:0016284,primitive neuroectodermal tumor of the cervix uteri,"['cervical malignant peripheral neuroectodermal tumor', 'malignant peripheral neuroectodermal tumor of the cervix uteri', 'malignant peripheral neuroectodermal tumour of the cervix uteri', 'peripheral neuroectodermal cancer of cervix uteri', 'cervical peripheral neuroectodermal cancer', 'cervical malignant peripheral neuroectodermal tumour']",,,213812,CN201074,,,,,,C53.0,,
mondo:0016285,papillary carcinoma of the cervix uteri,"['uterine cervix papillary carcinoma', 'cervical papillary carcinoma']",,,213817,CN201075,,,,,,C53.0,,
mondo:0016287,adenoid basal carcinoma of the cervix uteri,"['skin adenoid basal cell carcinoma of uterine cervix', 'uterine cervix skin adenoid basal cell carcinoma', 'cervical adenoid basal carcinoma']",,,213828,CN201077,,,,,,C53.0,,
mondo:0016289,malignant germ cell tumor of cervix uteri,"['cervical malignant germ cell tumor', 'germ cell cancer of the cervix uteri', 'malignant germ cell tumor of the cervix uteri', 'germ cell cancer of cervix uteri', 'uterine cervix malignant germ cell tumor', 'uterine cervix malignant germ cell tumour', 'cervical malignant germ cell tumour', 'cervical germ cell cancer', 'malignant germ cell tumour of the cervix uteri']",,,213837,CN201079,,,,,,C53.0,,
mondo:0016290,Hernández-Aguirre Negrete syndrome,"['intellectual disability-epilepsy-bulbous nose syndrome', 'Ehlers-Danlos syndrome with progeroid facies and mild mental retardation', 'Ehlers-Danlos syndrome with progeroid facies and mild intellectual disability']",,,2139,,,,,C538112,,,,
mondo:0016291,"craniosynostosis, Herrmann-Opitz type",['Herrmann Opitz craniosynostosis'],,,2145,CN226893,,,,,,,,
mondo:0016292,nodular neuronal heterotopia,"['hereditary nodular heterotopia', 'genetic nodular heterotopia']",,,2149,,"['-0.0578', '0.112', '0.0555', '-0.02179', '0.056', '-0.0841', '-0.02562', '0.006287', '-0.05066', '-0.01375', '-0.0804', '-0.00278', '-0.04855', '-0.02657', '-0.01141', '-0.0386', '-0.011696', '-0.06354', '0.0008783', '-0.1606', '-0.001916', '-0.0745', '0.1182', '-0.0745', '0.01714', '-0.02068', '-0.0164', '0.00824', '-0.04105', '-0.0207', '0.09924', '0.00577', '0.1433', '0.01768', '0.07324', '0.01555', '-0.02309', '-0.02428', '-0.02165', '-0.1057', '0.02556', '-0.1388', '0.06076', '-0.064', '-0.00349', '-0.09283', '-0.03455', '0.1067', '-0.03748', '0.05942', '0.06854', '-0.01367', '-0.02278', '0.003431', '-0.0908', '-0.10443', '0.1481', '-0.08325', '-0.1313', '0.00622', '0.0707', '0.0636', '-0.04623', '0.0472', '0.01323', '-0.004044', '0.154', '0.07587', '-0.0513', '0.1111', '-0.05856', '-0.003336', '0.04788', '-0.03867', '0.01251', '0.01567', '0.04813', '0.01017', '-0.0877', '-0.078', '-0.00163', '-0.0396', '-0.0217', '0.10046', '-0.04376', '-0.026', '0.04376', '0.09814', '0.0681', '-0.01441', '0.06415', '0.0716', '0.00422', '0.04004', '0.207', '-0.0008793', '0.1494', '-0.1106', '0.01924', '0.03516']",,,,,,,
mondo:0016293,congenital stationary night blindness,"['night blindness, congenital stationary', 'congenital essential nyctalopia']",0050534,,215,,,,,C536122,368.61,,,
mondo:0016294,Hirschsprung disease-type D brachydactyly syndrome,"['familial Hirschsprung^s disease and type D brachydactyly', 'Hirschsprung disease type d brachydactyly', 'Hirschsprung disease with type d brachydactyly', 'Hirschsprung disease with type D brachydactyly']",,306980,2150,C1844017,,,,C538319,,,,
mondo:0016295,neuronal ceroid lipofuscinosis,"['NCL', 'ceroid lipofuscinoses', 'hereditary ceroid lipofuscinosis']",14503,,216,C0027877,,C61257,,,,E75.4,,
mondo:0016296,holoprosencephaly,"['holoprosencephaly sequence', 'HPE']",4621,,2162,C0079541,"['-0.19', '0.1768', '0.2195', '-0.1262', '0.04095', '-0.3516', '0.8237', '0.495', '-1.121', '0.07526', '-0.8447', '-0.7217', '0.3254', '0.5225', '0.2737', '-0.5205', '-0.1425', '-0.1533', '-0.574', '-0.284', '-0.2463', '0.1084', '1.189', '-0.02657', '0.458', '-0.4062', '0.05566', '-0.092', '0.1482', '-0.06335', '0.5703', '0.0977', '0.7217', '0.2773', '0.2507', '-0.12115', '-0.1225', '-0.6777', '-0.602', '-0.5034', '-0.01643', '-0.05112', '0.3755', '-0.4531', '0.653', '-0.1584', '0.2625', '-0.2893', '-0.4348', '0.3413', '0.0792', '-0.05704', '-0.6187', '-0.1708', '-0.5117', '-0.07074', '0.3013', '-0.1637', '0.2944', '0.636', '-0.3887', '0.1594', '0.392', '0.2568', '-0.5137', '0.0923', '-0.03195', '0.10345', '-0.879', '0.05353', '-0.2056', '0.3066', '0.412', '0.2432', '-0.2703', '-0.0997', '0.666', '-0.05966', '-0.0598', '-0.1965', '-0.3264', '-0.34', '-0.2844', '0.6074', '0.04266', '-0.1799', '0.00881', '0.5054', '0.2195', '-0.01101', '0.0538', '0.5356', '0.4363', '0.09454', '0.582', '-0.6416', '0.568', '-0.2822', '0.648', '0.2766']",C74988,,D016142,,Q04.2,10056304,
mondo:0016297,prelingual non-syndromic genetic hearing loss,"['isolated prelingual genetic deafness', 'prelingual non-syndromic genetic deafness']",,,216445,,,,,,,,,
mondo:0016298,postlingual non-syndromic genetic hearing loss,['isolated postlingual genetic deafness'],,,216452,,,,,,,,,
mondo:0016299,holoprosencephaly-caudal dysgenesis syndrome,,,,2165,CN201097,,,,,,Q04.2,,
mondo:0016301,congenitally corrected transposition of the great arteries,"['levo-transposition of the great vessels', 'L-transposition of the great arteries', 'congenitally corrected transposition of the great vessels', 'transposition of the great vessels, congenitally corrected', 'ventriculoarterial and atrioventricular discordance', 'ventricular inversion', 'transposition of the great arteries, congenitally corrected', 'discordant ventriculoarterial and atrioventricular connections', 'Double discordance', 'levo-transposition of the great arteries', 'L-transposition of the great vessels']",,,216694,C3274488,,C98902,,D000080041,745.12,,10011120,
mondo:0016302,isolated congenitally uncorrected transposition of the great arteries,['isolated congenitally uncorrected transposition of the great vessels'],,,216718,,,,,,,,,
mondo:0016303,congenitally uncorrected transposition of the great arteries with cardiac malformation,"['TGA with cardiac malformation', 'congenitally uncorrected transposition of the great vessels with cardiac malformation']",,,216729,,,,,,,,,
mondo:0016304,classic pantothenate kinase-associated neurodegeneration,"['NBIA1, classic form', 'neurodegeneration with brain iron accumulation type 1, classic form', 'PKAN, classic form']",,,216866,CN201109,"['-0.1438', '0.3708', '0.1027', '-0.00874', '-0.156', '-0.5596', '-0.085', '0.2035', '-0.2986', '-0.04346', '-0.203', '0.01932', '-0.07355', '0.1428', '0.3523', '-0.2468', '-0.1396', '-0.3618', '0.07916', '-0.4272', '0.03595', '-0.2783', '0.0964', '-0.1882', '0.005653', '0.0757', '0.1437', '-0.2021', '-0.4492', '-0.079', '0.2212', '0.166', '0.3584', '0.2488', '0.083', '-0.03195', '-0.2118', '-0.3408', '-0.2054', '0.0474', '0.2507', '-0.364', '-0.1956', '0.164', '0.1722', '-0.1553', '-0.1514', '0.1841', '-0.0624', '0.1544', '-0.0208', '0.2417', '-0.0673', '-0.261', '0.1807', '-0.3022', '0.4277', '-0.0807', '-0.14', '0.06586', '-0.03485', '0.00461', '0.009895', '-0.1395', '-0.3472', '-0.1054', '0.4265', '0.3623', '-0.1328', '0.2115', '0.01834', '-0.1741', '0.1365', '-0.2673', '0.2145', '0.1729', '-0.03845', '0.03546', '-0.04858', '-0.2852', '0.0838', '-0.4033', '-0.0541', '0.3115', '0.216', '0.2449', '0.10034', '0.0002174', '0.4783', '0.1978', '0.371', '0.3103', '0.1409', '0.136', '0.362', '0.2158', '0.4202', '0.2284', '0.02635', '0.01614']",,,,,,,
mondo:0016305,atypical pantothenate kinase-associated neurodegeneration,"['NBIA1, atypical form', 'PKAN, atypical form', 'neurodegeneration with brain iron accumulation type 1, atypical form']",,,216873,CN201110,,,,,,,,
mondo:0016306,"Niemann-Pick disease type C, severe perinatal form",,,,216972,CN201112,,,,,,,,
mondo:0016307,"Niemann-Pick disease type C, severe early infantile neurologic onset",,,,216975,CN201113,,,,,,,,
mondo:0016308,"Niemann-Pick disease type C, late infantile neurologic onset",,,,216978,CN201114,,,,,,,,
mondo:0016309,"Niemann-Pick disease type C, juvenile neurologic onset","['Niemann-Pick disease type C, classic form']",,,216981,CN201115,,,,,,,,
mondo:0016310,"Niemann-Pick disease type C, adult neurologic onset",,,,216986,CN201116,,,,,,,,
mondo:0016311,Bockenheimer syndrome,['genuine diffuse phlebectasia'],,,217008,CN201119,,,,,,,,
mondo:0016312,5-fluorouracil poisoning,['5-fluorouracil intoxication'],,,217064,CN201128,,,,C531667,,,,
mondo:0016315,"mucopolysaccharidosis type 2, severe form","['MPSIIA', 'MPS2A', 'iduronate 2-sulfatase deficiency type A', 'mucopolysaccharidosis type II, severe form', 'mucopolysaccharidosis type IIA', 'Hunter syndrome type A', 'mucopolysaccharidosis type 2A']",,,217085,CN201131,,,,,,,,
mondo:0016316,"mucopolysaccharidosis type 2, attenuated form","['MPSIIB', 'mucopolysaccharidosis type II, attenuated form', 'iduronate 2-sulfatase deficiency type B', 'Hunter syndrome type B', 'mucopolysaccharidosis type IIB', 'mucopolysaccharidosis type 2B', 'MPS2B']",,,217093,CN201132,,,,,,,,
mondo:0016318,progressive multifocal leukoencephalopathy,"['progressive multifocal leukoencephalitis', 'leukoencephalopathy, progressive multifocal', 'PML']",643,,217260,C0023524,,C26815,0007455,D007968,046.3,A81.2,10036807,
mondo:0016319,congenital insensitivity to pain with hyperhidrosis,"['congenital indifference to pain with hyperhidrosis', 'congenital absence of pain with hyperhidrosis', 'congenital analgesia with hyperhidrosis']",,,217399,,,,,,,,,
mondo:0016321,pulmonary interstitial glycogenosis,"['infantile cellular interstitial pneumonitis', 'pig']",,,217557,C3161106,,,,,,J84.842,,
mondo:0016322,neuroendocrine cell hyperplasia of infancy,"['CTI', 'NCHI', 'chronic tachypnoe of infancy', 'NEHI']",,,217560,C3161105,,C120169,,,,J84.841,,
mondo:0016323,chronic respiratory distress with surfactant metabolism deficiency,,,,217566,,,,,,,,,
mondo:0016330,non-familial hypertrophic cardiomyopathy,['acquired hypertrophic cardiomyopathy'],,,217598,CN226903,,,,,,,,
mondo:0016331,infantile systemic hyalinosis,,,236490,2176,,,,,,,,,
mondo:0016332,hypertrophic cardiomyopathy due to intensive athletic training,,,,217601,CN226904,,,,,,,,
mondo:0016333,familial dilated cardiomyopathy,"['hypokinetic dilated cardiomyopathy, familial', 'hereditary dilated cardiomyopathy', 'idiopathic dilated cardiomyopathy', 'DCM', 'dilated cardiomyopathy, familial']",,,217607,C0340427,"['-0.2786', '-0.389', '0.0659', '0.541', '0.5767', '-0.493', '0.233', '0.5317', '0.11536', '-0.2527', '0.654', '-0.1842', '-0.8', '0.3452', '-0.599', '-0.8027', '-0.7046', '0.1957', '-0.591', '-0.817', '0.345', '0.675', '0.04718', '-0.03029', '-0.3188', '-0.5303', '-0.4282', '0.6304', '-0.1428', '0.00946', '0.9385', '-0.11017', '0.6797', '-0.0653', '-0.1583', '-0.4094', '-0.01889', '-0.3188', '0.6895', '-0.728', '-0.057', '0.392', '0.4456', '0.3135', '0.4653', '0.2793', '-0.1848', '0.3735', '0.5103', '0.02759', '-0.11115', '-0.278', '0.587', '-0.4163', '-0.0428', '-0.676', '-0.4426', '0.4688', '-0.5356', '-0.1644', '-0.03912', '0.477', '-0.1912', '-0.392', '-0.8237', '0.2996', '-0.06094', '0.7236', '-0.6694', '0.1727', '-0.3743', '0.152', '0.575', '-0.6353', '-0.0118', '0.4304', '0.2607', '-0.0642', '0.001837', '0.01322', '0.3962', '-0.4937', '0.1221', '-0.4175', '0.8584', '0.1859', '0.3916', '0.04517', '0.6455', '0.09717', '0.07965', '0.2145', '-0.585', '0.4292', '0.564', '0.323', '-0.1938', '-0.01448', '-0.705', '0.0781']",,,C536231,,,,
mondo:0016338,non-familial dilated cardiomyopathy,,,,217629,CN226906,,,,,,,,
mondo:0016340,familial restrictive cardiomyopathy,['hereditary restrictive cardiomyopathy'],,,217635,,"['0.326', '-0.769', '-0.1915', '0.5806', '0.0824', '-0.5166', '0.668', '0.7163', '-0.4385', '-0.405', '0.529', '-0.2961', '-0.344', '0.573', '-0.6206', '0.262', '-0.7124', '-0.09467', '-0.762', '-0.585', '0.321', '0.3894', '0.756', '-0.209', '0.502', '-0.2179', '0.2917', '0.266', '-0.01689', '-0.242', '0.903', '-0.38', '0.9146', '0.2355', '0.11505', '-0.569', '-0.4685', '-0.595', '0.7593', '-0.526', '0.07587', '0.6895', '0.02458', '0.649', '0.3518', '0.3687', '0.33', '0.732', '0.7837', '-0.4482', '-0.3555', '0.27', '0.729', '-0.0959', '0.5083', '-0.5464', '-0.4568', '0.448', '-0.7114', '-0.3381', '0.06137', '0.5396', '0.3481', '-1.062', '-1.004', '0.3838', '0.2382', '0.649', '-0.7207', '0.0811', '-0.4197', '0.3008', '-0.03625', '-0.2162', '-0.0838', '0.778', '-0.5005', '0.07855', '-0.4998', '0.3008', '-0.05093', '-0.1786', '-0.2147', '-0.478', '1.131', '-0.1827', '0.441', '0.04993', '0.863', '0.2095', '0.09406', '-0.00922', '-0.2537', '0.26', '0.9995', '1.078', '-0.01045', '-0.47', '-0.2922', '-0.0903']",,,,425.4,,,
mondo:0016342,familial isolated arrhythmogenic right ventricular dysplasia,"['familial isolated arrhythmogenic ventricular cardiomyopathy', 'familial isolated ARVC', 'familial isolated ARVD', 'familial isolated arrhythmogenic right ventricular cardiomyopathy', 'familial isolated arrhythmogenic ventricular dysplasia']",,,217656,CN226907,"['-0.1116', '-0.010376', '0.11426', '-0.231', '0.1292', '-0.3088', '0.563', '-0.02087', '0.3374', '-0.3115', '-0.3418', '-0.631', '-0.6084', '0.4119', '-0.5674', '0.04956', '-0.887', '-0.3582', '0.1664', '-1.263', '0.408', '0.6562', '0.5054', '-0.1848', '-0.3025', '-0.11816', '0.198', '0.2458', '0.1802', '-0.02087', '0.2769', '0.5483', '0.356', '0.2952', '-0.1338', '-0.5293', '0.3022', '0.03357', '0.416', '-0.4988', '0.417', '-0.3035', '0.47', '0.01496', '-0.2428', '0.27', '-0.7393', '0.5303', '0.274', '0.321', '0.3152', '0.4883', '0.538', '-0.1094', '-0.0004635', '-0.546', '0.346', '-0.2412', '-0.2905', '-0.206', '0.1054', '0.2053', '0.1992', '-0.4805', '-0.2196', '0.04773', '0.8706', '0.728', '-0.367', '-0.0916', '-0.3237', '-0.2389', '0.4424', '-0.43', '0.08655', '0.07117', '-0.2612', '-0.06366', '-0.3572', '-0.282', '-0.0983', '0.3918', '-0.003944', '-0.311', '0.4146', '0.00784', '0.2302', '0.06012', '0.08777', '-0.1204', '-0.003803', '-0.2296', '0.3037', '0.246', '0.897', '0.6055', '0.8633', '-0.488', '-0.532', '0.2502']",,,,,,,
mondo:0016344,hydranencephaly,"['hydranencephaly', 'Hydroanencephaly', 'hydranencephaly (disease)']",4626,,2177,C0020225,,C98949,,D006832,,,,0002324
mondo:0016345,non-familial restrictive cardiomyopathy,,,,217720,CN226908,,,1001473,,,,,
mondo:0016346,hydrocephalus-obesity-hypogonadism syndrome,"['hydrocephalus obesity hypogonadism', 'congenital hydrocephalus oligophrenia dwarfism centripetal obesity and hypogonadism', 'Sengers-Hamel-Otten syndrome']",,,2183,CN201182,,,,,,,,
mondo:0016348,non-genetic cardiac rhythm disease,,,,218439,CN201186,,,,,,,,
mondo:0016349,congenital hydrocephalus,"['HYC3', 'congenital hydrocephalus']",,,2185,C0020256,"['-0.2466', '-0.04947', '-0.00897', '0.2703', '-0.3374', '-0.28', '-0.1594', '0.635', '-0.472', '0.6934', '-0.1026', '-0.9365', '-0.4417', '0.4875', '0.4053', '-0.2966', '-0.6533', '-0.1738', '-0.655', '-1.099', '-0.1626', '-0.3691', '0.464', '-0.401', '-0.1362', '-0.653', '-1.04', '0.8374', '-0.517', '0.595', '-0.2194', '-0.873', '0.5215', '-0.1353', '-0.516', '0.5205', '-0.1528', '0.03903', '-0.00676', '-0.291', '0.782', '0.3809', '0.143', '-0.599', '0.8813', '-0.03223', '0.566', '-0.5474', '0.5586', '0.3943', '0.309', '0.01148', '-0.309', '-1.012', '0.1119', '-0.2041', '0.0847', '0.227', '0.1338', '0.4065', '-0.2325', '0.6807', '-0.5156', '-0.0784', '-0.02255', '0.2463', '0.1658', '0.0286', '-0.8086', '0.1111', '-0.02196', '1.114', '0.1556', '-0.979', '0.2047', '0.38', '0.464', '0.8237', '-0.2773', '-1.007', '-0.2217', '-0.1716', '-0.5293', '0.4802', '0.4255', '0.913', '0.577', '0.09296', '0.3794', '-0.4363', '-0.1783', '0.882', '0.2568', '0.04376', '0.7563', '0.4963', '0.5537', '-0.1726', '-0.09985', '0.3057']",C98876,,,,Q03,10010506,
mondo:0016350,hydrocephalus-blue sclerae-nephropathy syndrome,"['Daentl-Townsend-Siegel syndrome', 'familial nephrosis, hydrocephalus, thin skin, blue sclerae syndrome', 'hydrocephalus blue sclera nephropathy']",,,2186,,,,,C535768,,,,
mondo:0016351,anti-HLA hyperimmunization,,,,2194,CN201194,,,,,,,,
mondo:0016352,idiopathic inherited hypercalciuria,['idiopathic hypercalciuria'],,,2197,,"['-0.08453', '-0.2263', '0.0324', '0.072', '-0.0887', '0.04803', '-0.10767', '0.9453', '-0.4417', '0.677', '-0.343', '0.09283', '-0.2947', '0.5234', '-0.3186', '-0.2976', '-0.10913', '0.4084', '-0.12286', '-0.447', '0.1532', '-0.6646', '0.6475', '-0.1656', '0.2048', '-0.001902', '0.02739', '-0.1241', '-0.566', '0.3826', '0.3774', '-0.5054', '0.3757', '0.0535', '-0.32', '0.2395', '-0.0403', '0.07935', '0.2001', '-0.1901', '-0.2018', '-0.194', '0.5684', '-0.598', '0.2576', '-0.6426', '0.007004', '-0.2388', '0.08386', '0.4229', '-0.3372', '0.04257', '0.3096', '-0.4243', '-0.3242', '-0.09705', '0.2297', '-0.352', '-0.7236', '-0.07983', '0.713', '0.4583', '-0.8335', '-0.6133', '0.5635', '0.543', '0.2292', '-0.08044', '0.0174', '-0.2717', '0.12396', '-0.05905', '-0.03445', '0.02222', '0.416', '0.1179', '-0.01895', '0.133', '-0.0684', '-0.00834', '-0.2059', '-0.375', '0.3005', '0.1617', '0.1223', '-0.002148', '0.2042', '-0.5195', '0.627', '-0.0828', '-0.03632', '0.3289', '-0.904', '-0.1865', '0.4043', '0.2903', '0.666', '-0.379', '-0.4758', '-0.0406']",,,,,,,
mondo:0016353,palmoplantar keratoderma-spastic paralysis syndrome,"['palmoplantar hyperkeratosis-spastic paralysis syndrome', 'keratoderma palmoplantar spastic paralysis', 'Powell-Venencie-Gordon syndrome']",,,2201,,,,,C538358,,,,
mondo:0016354,xeroderma pigmentosum-Cockayne syndrome complex,['XP/CS complex'],,,220295,CN201205,"['-0.08374', '0.7705', '-0.2264', '-0.1869', '0.06995', '-0.3171', '0.04822', '-0.2357', '0.2427', '-0.495', '-0.07635', '-0.05164', '-0.4692', '0.08203', '0.1166', '-0.5083', '0.3389', '-0.11993', '-0.1438', '-0.768', '0.1976', '-0.1566', '0.3416', '-0.468', '0.04556', '0.6426', '-0.4172', '0.2032', '-0.1658', '0.1637', '0.03378', '-0.03915', '0.6045', '0.2666', '0.398', '0.3542', '-0.01851', '-0.3682', '-0.562', '-0.06915', '0.3762', '-0.8154', '0.04764', '-0.06366', '0.3193', '-0.6523', '0.1577', '0.1293', '0.4524', '-0.321', '0.4683', '0.1321', '-0.035', '0.241', '-0.2025', '-0.3691', '0.664', '-0.1545', '-0.55', '-0.2152', '0.3438', '-0.1013', '-0.1853', '0.3826', '-0.2507', '0.2028', '0.255', '0.0668', '-0.1084', '0.4036', '-0.793', '-0.02383', '0.466', '0.0389', '0.0641', '-0.2344', '0.013504', '0.03467', '0.3062', '-0.03455', '0.2644', '0.3337', '0.102', '0.4722', '0.1476', '-0.06976', '0.731', '0.4705', '0.4033', '0.2163', '1.008', '0.8926', '0.1842', '-0.06476', '0.156', '0.1727', '0.3496', '-0.04535', '0.462', '0.2686']",C156031,,,,Q82.1,,
mondo:0016355,semilobar holoprosencephaly,,,,220386,,,,,,,,,
mondo:0016356,diffuse cutaneous systemic sclerosis,"['diffuse cutaneous systemic scleroderma', 'DcSSc', 'dSSc', 'progressive cutaneous systemic scleroderma', 'progressive cutaneous systemic sclerosis']",,,220393,,,C116791,,,,,,
mondo:0016357,dysplastic cortical hyperostosis,,,,646139,CN201209,,,,,,,,
mondo:0016358,limited cutaneous systemic sclerosis,"['systemic sclerosis, limited', 'limited cutaneous systemic scleroderma', 'limited scleroderma']",1577,,220402,C0748540,,,1001017,D045745,,,,
mondo:0016359,limited systemic sclerosis,"['systemic sclerosis sine scleroderma', 'Scleroderma, sine', 'SSC without skin involvement', 'systemic sclerosis without skin involvement', 'progressive systemic sclerosis sine scleroderma']",,,220407,C1290138,,C116789,,,,,,
mondo:0016360,marcothrombocytopenia with mitral valve insufficiency,,,,220448,,,,,,,,,
mondo:0016361,isolated hereditary giant platelet disorder,"['isolated hereditary macrothrombocytopenia', 'isolated inherited macrothrombocytopenia', 'isolated inherited giant platelet disorder']",,,220452,CN226911,,,,,,,,
mondo:0016362,attenuated familial adenomatous polyposis,"['attenuated FAP', 'attenuated familial adenomatous polyposis', 'AFAP', 'attenuated familial polyposis coli', 'hereditary flat adenoma syndrome', 'mild form of FAP', 'AAPC', 'HFAS', 'attenuated adenomatous polyposis coli']",,,220460,C2674616,"['0.0388', '0.36', '-0.3835', '-0.02599', '0.00492', '-0.637', '-0.26', '1.0205', '-0.625', '-0.045', '0.4836', '0.7085', '-0.2344', '-0.0962', '0.1321', '-0.1898', '0.2844', '-0.3813', '0.7603', '-0.5195', '0.2979', '0.4907', '0.3943', '-0.5874', '1.015', '0.10547', '0.45', '0.02448', '-0.3452', '-0.8076', '0.4604', '-0.5635', '-0.01513', '-0.00613', '-0.01328', '0.0692', '-0.7734', '0.08466', '-0.0714', '-0.2141', '0.648', '-0.6333', '-0.7686', '-0.0253', '0.1638', '0.02554', '-0.3481', '0.002718', '0.506', '0.0352', '0.12463', '0.0902', '-0.476', '0.05817', '-0.468', '-0.557', '-0.652', '0.4858', '-0.944', '-0.3782', '1.106', '0.2893', '0.697', '0.10864', '-0.01616', '0.2686', '0.3225', '0.3552', '-0.8374', '-0.0282', '0.302', '0.2065', '0.687', '0.08563', '0.3545', '0.626', '0.203', '0.3271', '-0.04453', '-0.2695', '-0.1577', '0.11255', '0.04968', '-0.3955', '-0.743', '-0.4187', '0.181', '0.09955', '0.2776', '-0.1467', '-0.0537', '0.196', '-0.02458', '-0.1598', '0.685', '-0.2654', '0.752', '-0.655', '-0.639', '0.01588']",C6729,,C538265,,,,
mondo:0016364,Joubert syndrome with ocular defect,"['JBTS3', 'Joubert syndrome with retinopathy', 'Joubert syndrome 3', 'Joubert syndrome with ocular anomalies', 'JS-O']",,,220493,CN201217,"['-0.11725', '0.06366', '-0.0751', '-0.07965', '0.1544', '-0.414', '-0.2192', '-0.05493', '-0.2583', '0.01168', '-0.3184', '-0.582', '-0.1771', '-0.1199', '0.2158', '-0.5327', '0.2751', '-0.2225', '0.05374', '-1.248', '-0.3352', '0.1274', '0.6187', '0.299', '-0.1692', '0.2986', '-0.5996', '-0.0719', '0.2644', '-0.00553', '0.3352', '0.406', '0.5273', '0.3943', '-0.0001659', '0.0006557', '-0.26', '-0.077', '-0.5312', '-0.3687', '0.4275', '-0.4941', '0.2357', '0.10046', '-0.02309', '-0.06805', '-0.1454', '0.01108', '0.2261', '0.3352', '0.2314', '0.434', '0.02809', '-0.6445', '-0.1952', '-0.505', '0.5786', '-0.1305', '-0.1703', '0.1366', '0.1998', '-0.1584', '0.6597', '0.3213', '0.2184', '0.05765', '0.4019', '0.4626', '-0.684', '0.509', '-0.1508', '0.17', '0.285', '0.2239', '0.6934', '-0.1404', '0.4773', '-0.4695', '-0.04764', '0.02467', '0.3196', '-0.04544', '-0.2435', '0.6206', '-0.4194', '-0.3', '0.2761', '0.4358', '0.327', '-0.0224', '-0.0989', '0.4224', '0.3726', '0.1664', '0.384', '-0.002296', '0.5405', '-0.08374', '-0.239', '0.519']",,,,,H35.5,,
mondo:0016365,familial primary hyperparathyroidism,['hereditary primary hyperparathyroidism (disease)'],,,2207,CN201220,,,,,,,,
mondo:0016366,maternal phenylketonuria,"['maternal hyperphenylalaninemia', 'phenylketonuric embryopathy', 'maternal PKU', 'hyperphenylalaninemic embryopathy']",,,2209,,"['-0.3813', '-0.2825', '0.4312', '-0.01991', '0.6646', '-0.007523', '-0.1385', '0.7354', '-0.3782', '0.1731', '-0.3909', '0.07886', '0.7715', '-0.0691', '-0.4685', '-0.613', '-0.03986', '0.3232', '-0.5845', '-0.4756', '0.3384', '-0.2401', '0.6157', '-0.3665', '0.2216', '-0.2908', '-0.52', '0.1688', '0.346', '0.0799', '0.5205', '-0.4045', '0.7793', '-0.06396', '-0.617', '-0.02464', '0.4207', '0.2129', '0.408', '-0.355', '-0.1497', '0.0787', '0.441', '-0.6255', '-0.11163', '-0.4534', '0.5034', '0.566', '-0.646', '0.0521', '-0.3625', '-0.4856', '-0.1978', '-0.8423', '-0.509', '0.2998', '0.02502', '0.1406', '-0.1688', '0.4094', '-0.5664', '0.232', '0.0678', '-0.223', '0.1274', '0.0942', '0.103', '0.1926', '-0.7583', '0.536', '0.2438', '0.7466', '0.63', '0.1837', '-0.05615', '0.513', '-0.1284', '-1.0', '-0.7754', '0.1888', '-0.0385', '-0.1462', '-0.1384', '0.569', '0.3403', '0.846', '-0.4297', '-0.3096', '0.4397', '0.764', '0.2842', '0.1885', '-0.236', '-0.03915', '0.3894', '0.1667', '0.1733', '-0.3645', '0.11597', '-0.2197']",,,D017042,,,,
mondo:0016367,dermatomyositis,"['Amyopathic dermatomyositis', 'dermatomyositis', 'DM', 'polymyositis with skin involvement', 'adult dermatomyositis', 'dermatopolymyositis']",10223,,221,C0011633,,C26744,0000398,D003882,710.3,,10012503,
mondo:0016368,Rothmund-Thomson syndrome type 1,"['Poikiloderma Atrophicans and Cataract', 'RTS1', 'ROTHMUND-THOMSON SYNDROME, TYPE 1', 'poikiloderma of Rothmund-Thomson type 1']",,618625,221008,CN201233,"['0.2905', '0.3015', '0.1482', '-0.5522', '0.1095', '-0.518', '0.0819', '0.8447', '0.07855', '-0.6094', '0.1431', '0.3657', '-0.08936', '-0.2778', '-0.2905', '0.1661', '0.9355', '-0.3787', '-0.1613', '-0.3967', '-0.2043', '-0.231', '-0.05334', '-0.4758', '0.2162', '0.659', '0.04144', '-0.264', '0.396', '-0.1901', '0.309', '0.161', '0.546', '0.227', '0.6216', '-0.04044', '-0.3867', '-0.2341', '-0.00413', '-0.06122', '0.3672', '-0.502', '-0.01671', '-0.3962', '0.05475', '0.314', '0.006874', '0.2979', '0.2559', '-0.55', '0.002605', '-0.0082', '-0.1747', '-0.3088', '-0.4175', '-0.3755', '0.01706', '-0.487', '-0.6865', '-0.4055', '0.342', '-0.1148', '0.04855', '-0.4412', '0.3484', '0.2025', '0.4263', '0.4465', '0.2174', '0.809', '-0.395', '-0.214', '0.1274', '-0.246', '0.17', '-0.319', '-0.1804', '-0.02394', '0.1088', '0.2457', '0.2246', '-0.1243', '-0.03995', '-0.03986', '-0.4885', '-0.427', '0.1464', '0.011894', '0.316', '0.4705', '0.2974', '0.653', '0.798', '0.3245', '0.595', '0.1503', '0.566', '-0.5195', '0.0795', '-0.1661']",C178826,,,,,,
mondo:0016369,Rothmund-Thomson syndrome type 2,"['Rothmund-Thomson syndrome, type 2', 'RTS2', 'poikiloderma of Rothmund-Thomson type 2']",,268400,221016,CN201234,,C178827,,,,,,
mondo:0016370,Marchiafava-Bignami disease,"['chronic Marchiafava-Bignami syndrome', 'metabolic bone disease', 'Marchiafava Bignami disease', 'metabolic bone disorder', 'MBD', 'acute Marchiafava-Bignami disease']",,,221074,C0238265,,C97045,1001809,D054319,341.8,,10026828,
mondo:0016371,combined hyperactive dysfunction syndrome of the cranial nerves,,,,221078,CN201241,,,,,,,,
mondo:0016372,glossopharyngeal neuralgia,"['glossopharyngeal neuralgia', 'glossopharyngeal nerve neuralgia', 'Glossovasopharyngeal neuralgia', 'neuralgia of glossopharyngeal nerve']",14423,,221098,C0154731,,,,,352.1,,10018391,
mondo:0016373,isolated facial myokymia,,,,221106,,,,,,,G51.4,,
mondo:0016374,cranial neuralgia,"['cranial neuron projection bundle neuralgia', 'facial neuralgia', 'neuralgia of cranial neuron projection bundle']",,,221109,C0010269,,,,,,,,
mondo:0016375,acquired peripheral movement disorder,,,,221114,CN226913,,,,,,,,
mondo:0016376,confetti-like macular atrophy,,,,221142,,,,,,,,,
mondo:0016377,Pitt-Hopkins-like syndrome,['PTHSL'],,,221150,CN239445,"['-0.1995', '0.07404', '0.1886', '-0.2058', '0.0341', '-0.2886', '0.1635', '0.5303', '-0.5615', '0.03958', '-0.02455', '-0.10645', '0.1881', '-0.05438', '0.1433', '0.02394', '0.2251', '-0.01682', '-0.1815', '-0.5522', '-0.1293', '0.0174', '0.11194', '-0.2008', '0.14', '-0.133', '-0.1777', '-0.244', '0.1663', '-0.1318', '-0.0199', '0.09656', '0.3074', '0.2668', '0.000346', '-0.0195', '-0.1823', '-0.1533', '-0.03635', '-0.327', '0.3809', '-0.08923', '-0.3406', '0.1729', '0.11237', '-0.377', '-0.1312', '0.2097', '0.03873', '0.3967', '-0.5146', '0.1569', '-0.09766', '0.035', '0.0542', '-0.04272', '-0.1603', '-0.272', '0.00768', '-0.04404', '0.151', '0.2317', '0.2191', '0.1738', '-0.0676', '-0.10547', '0.27', '0.3276', '-0.0871', '0.2527', '-0.3955', '0.2191', '0.02124', '-0.0371', '0.06018', '0.148', '0.2722', '-0.0638', '-0.2347', '0.1073', '0.085', '-0.0991', '-0.02657', '0.3892', '0.1724', '0.1537', '-0.04367', '0.3806', '0.2484', '0.3696', '0.0761', '0.4253', '0.287', '0.1885', '0.3145', '0.3333', '0.07117', '-0.2979', '0.4624', '0.1449']",,,,,,,
mondo:0016378,maternal hyperthermia induced birth defects,['hyperthermia induced defects'],,,2216,C0265377,,,,,,,,
mondo:0016379,erosive pustular dermatosis of the scalp,,,,222,C0406464,,,,,,,,
mondo:0016380,acquired hypertrichosis lanuginosa,"['hypertrichosis lanuginosa, acquired']",,,2221,CN201274,,,,,,L68.1,,
mondo:0016381,hypertrichosis lanuginosa congenita,"['hypertrichosis lanuginosa congenita', 'hypertrichosis universalis', 'congenital hypertrichosis lanuginosa', 'hypertrichosis lanuginosa universalis']",,145700,2222,,,,,C538389,,,,
mondo:0016382,hereditary poikiloderma,,,,222628,,,,,,,,,
mondo:0016383,nephrogenic diabetes insipidus,"['ADH resistant diabetes insipidus', 'vasopressin-resistant diabetes insipidus', 'diabetes insipidus nephrogenic', 'diabetes insipidus nephrogenic type 1', 'diabetes insipidus nephrogenic X-linked']",12387,,223,C0162283,"['0.7017', '-0.2856', '0.012276', '0.7285', '-0.481', '-0.867', '-0.2007', '0.9497', '0.10406', '-0.408', '0.1182', '-0.1841', '0.2646', '0.10406', '-0.971', '-0.3782', '0.4048', '0.2012', '0.1951', '-0.4797', '0.057', '-0.2783', '-0.03476', '-0.01461', '-0.576', '-0.3079', '0.11255', '0.0932', '0.3657', '-0.3413', '0.819', '-0.639', '0.1584', '-0.1777', '-0.2065', '0.511', '-0.4102', '0.5864', '0.09595', '-0.3965', '0.0735', '0.518', '0.1951', '0.3547', '-0.4517', '-0.4355', '0.3188', '-0.1844', '-0.04865', '0.461', '0.11774', '-0.4463', '0.7197', '-0.7456', '-0.0693', '0.2124', '-0.04327', '-0.7007', '-0.9873', '0.4104', '-0.103', '0.603', '-0.1705', '0.1948', '0.03616', '0.7603', '-0.3982', '0.457', '-0.92', '0.4937', '0.5044', '0.2727', '-0.02606', '-0.286', '0.6055', '0.4275', '-0.5996', '0.909', '-0.3462', '-0.1908', '0.0788', '0.0456', '0.03873', '-0.3743', '0.0913', '0.2705', '0.0722', '0.6807', '0.7646', '0.0937', '0.4666', '0.146', '0.03024', '-0.3699', '1.088', '0.2566', '-0.161', '-0.2345', '-0.4229', '0.1482']",C84919,,D018500,588.1,N25.1,10029147,
mondo:0016384,hypogonadotropic hypogonadism-frontoparietal alopecia syndrome,['Salti-Salem syndrome'],,,2230,CN201280,,,,,,E23.0,,
mondo:0016385,hypogonadism-mitral valve prolapse-intellectual disability syndrome,"['primary gonadal failure, short stature, mitral valve prolapse, and mental retardation', 'Cantalamessa Baldini Ambrosi syndrome', 'primary gonadal failure, short stature, mitral valve prolapse, and intellectual disability', 'Cantalamessa-Baldini-Ambrosi syndrome']",,,2233,C2931685,,,,C537981,,,,
mondo:0016386,hypogonadotropic hypogonadism-retinitis pigmentosa syndrome,['Chang-Davidson-Carlson syndrome'],,,2235,C2931722,,,,C538075,,,,
mondo:0016387,mitochondrial oxidative phosphorylation disorder,"['OXPHOS disease', 'OXPHOS system deficiency']",,,223713,CN201288,"['-0.1812', '0.1162', '0.007072', '0.05585', '0.04697', '-0.1707', '0.009476', '0.1278', '-0.0943', '0.01534', '-0.0122', '-0.06238', '0.04926', '-0.03302', '0.03592', '-0.1033', '0.005817', '-0.0651', '-0.1159', '-0.2177', '0.00841', '-0.135', '0.149', '-0.04538', '0.009895', '-0.0433', '0.0183', '0.03226', '-0.03943', '-0.0673', '0.0669', '0.0989', '0.1982', '0.06238', '-0.02571', '-0.10333', '0.01098', '-0.0683', '-0.01985', '-0.085', '0.0679', '-0.1617', '-0.02583', '0.04776', '-0.10724', '-0.1418', '-0.006557', '0.1012', '0.0249', '0.0464', '-0.0825', '-0.0663', '0.02759', '0.002722', '-0.0673', '-0.0709', '0.1146', '-0.011246', '-0.04437', '0.05753', '0.0814', '0.03598', '0.1696', '-0.03372', '-0.0579', '0.0353', '0.1434', '0.0895', '-0.1746', '0.135', '-0.0618', '-0.012314', '0.01701', '-0.002747', '0.06183', '0.06714', '0.02142', '0.010475', '-0.0377', '0.04257', '0.02235', '0.03357', '-0.0469', '0.1076', '0.01315', '-0.01753', '0.0699', '0.1342', '0.1421', '0.02687', '0.12085', '0.06058', '-0.00825', '0.001415', '0.2352', '0.1148', '0.1276', '-0.1562', '0.01852', '0.04538']",,,,,,,
mondo:0016390,familial hypoparathyroidism,"['hypoparathyroidism familial isolated', 'familial isolated hypoparathyroidism', 'hypoparathyroidism, familial', 'hypoparathyroidism, familial isolated', 'FIH']",0111387,,2238,C1832648,"['-0.1821', '0.06204', '-0.1577', '-0.09863', '-0.5737', '0.6704', '-0.002863', '0.7896', '-1.033', '-1.166', '-0.1296', '-0.1925', '-0.563', '0.6104', '-0.2216', '0.531', '-0.013916', '0.01756', '-0.754', '-0.375', '0.1609', '-0.3264', '-0.04297', '-0.02701', '-0.03198', '-0.1799', '-0.401', '-0.1868', '0.583', '-1.003', '-0.0611', '0.2944', '-0.507', '0.1726', '-0.2546', '-0.164', '0.2983', '-0.01101', '0.4888', '0.319', '0.10126', '0.01153', '0.61', '-0.4282', '0.593', '-0.812', '0.5073', '0.1669', '-0.03958', '0.4146', '0.2817', '0.613', '0.8433', '-0.2236', '-0.658', '-0.9014', '-0.03964', '-0.3347', '-0.4307', '-0.2339', '0.315', '-0.2413', '0.2595', '-0.2695', '-0.5957', '1.171', '0.6934', '0.782', '-0.537', '-0.1364', '-0.06042', '-0.2175', '0.692', '-0.00248', '0.804', '0.412', '0.3', '0.2172', '0.1683', '0.872', '0.5103', '0.509', '0.0772', '-0.728', '0.285', '-0.5806', '-0.3127', '0.501', '0.469', '0.3047', '-0.02844', '0.526', '-0.276', '-0.251', '0.199', '0.349', '0.3584', '-0.98', '-0.01433', '0.6226']",,,C537156,,,,
mondo:0016391,neonatal diabetes mellitus,"['NDM', 'diabetes mellitus syndrome in newborn infant', 'congenital diabetes mellitus']",11717,,224,C0158981,,C99248,,,775.1,P70.2,10028933,
mondo:0016392,cerebellar hypoplasia-tapetoretinal degeneration syndrome,['cerebellar hypoplasia tapetoretinal degeneration'],0070339,,2246,,,,,,,,,
mondo:0016393,hyposmia-nasal and ocular hypoplasia-hypogonadotropic hypogonadism syndrome,"['Bosma arhinia-microphthalmia syndrome', 'Bosma-Henkin-Christiansen syndrome']",,,2250,CN201299,"['-0.4175', '0.01813', '0.3367', '-0.3499', '0.10803', '-0.1617', '-0.0737', '0.6206', '-0.2451', '-0.2449', '-0.2003', '-0.3467', '-0.2805', '-0.1783', '-0.074', '0.04254', '0.3237', '0.1059', '-0.3545', '-0.3496', '-0.2317', '-0.1028', '-0.04333', '-0.2451', '0.1827', '0.0595', '-0.1923', '0.1305', '0.4988', '-0.371', '0.387', '0.01944', '0.3047', '0.1558', '0.16', '-0.1349', '0.111', '-0.528', '-0.1659', '-0.3333', '0.5024', '0.04614', '-0.1327', '-0.1104', '0.0994', '-0.1049', '0.1082', '0.2003', '-0.4248', '-0.05206', '-0.035', '0.1483', '0.0697', '-0.001562', '-0.2927', '-0.1528', '0.2394', '-0.1912', '-0.3506', '0.2993', '0.1576', '0.03555', '-0.09', '0.2413', '-0.149', '-0.2256', '0.3064', '0.3755', '-0.2827', '0.2455', '-0.425', '0.1852', '0.262', '-0.1622', '0.05542', '-0.255', '0.2632', '-0.0436', '-0.1733', '0.1481', '0.3003', '0.209', '0.1351', '0.506', '-0.06976', '-0.06433', '-0.04422', '0.1141', '0.1876', '-0.08203', '0.06805', '0.614', '0.323', '-0.1373', '0.795', '-0.11505', '0.03473', '-0.4346', '0.2137', '0.1487']",,,,,,,
mondo:0016394,sporadic infantile bilateral striatal necrosis,"['ABSN', 'sporadic infantile striatonigral necrosis', 'sporadic infantile striatonigral degeneration', 'sporadic IBSN', 'acute bilateral striatal necrosis']",,,225147,,,,,,,G23.2,,
mondo:0016395,foveal hypoplasia-presenile cataract syndrome,['O^Donnell-Pappas syndrome'],,,2253,C2931644,,,,C537858,,,,
mondo:0016396,pontocerebellar hypoplasia type 1,"['PCH1', 'Norman disease', 'mental retardation, autosomal recessive 32', 'MRT32']",0112322,,2254,C1843504,"['-0.597', '0.4883', '0.02629', '-0.1873', '0.1388', '-0.9834', '-0.2625', '0.887', '-0.84', '-0.592', '-0.328', '-0.3528', '-0.262', '-0.3499', '0.368', '0.2329', '-0.2534', '-0.5776', '0.4163', '-0.669', '-0.1183', '-0.4238', '-0.0245', '-0.2445', '-0.2155', '0.03574', '-0.3389', '0.2104', '-0.11633', '-0.4294', '0.0327', '0.3416', '0.4775', '0.1914', '0.02185', '0.2313', '-0.2157', '0.2035', '-0.1654', '0.3162', '0.02385', '-0.548', '0.2578', '0.418', '-0.7896', '0.0877', '0.00838', '-0.4597', '0.2495', '-0.1346', '0.3374', '0.09753', '-0.3838', '-0.2277', '0.2693', '-0.6416', '0.1548', '0.03296', '0.0712', '0.709', '0.2037', '0.10095', '0.4666', '0.2668', '-0.3047', '-0.2239', '0.2568', '0.3926', '-0.573', '0.775', '-0.4302', '0.643', '0.0143', '0.1453', '0.355', '0.0379', '-0.1389', '-0.555', '-0.728', '0.592', '0.2976', '0.3826', '0.1013', '0.523', '-0.0891', '0.3892', '0.51', '0.778', '0.4138', '-0.313', '0.4368', '0.18', '0.0646', '-0.2225', '0.8486', '0.2651', '0.3599', '-0.2551', '1.154', '-0.03598']",,,C548069,,,,
mondo:0016407,oligomeganephronia,['Oligomeganephronic renal hypoplasia'],0111142,,2260,C0431694,,C123202,,,,Q60.4,,
mondo:0016408,permanent congenital hypothyroidism,,,,226292,,,,,,,,,
mondo:0016409,primary congenital hypothyroidism,,,,226295,,,,,,,,,
mondo:0016410,central congenital hypothyroidism,"['thyrotropin deficiency', 'central hypothyroidism', 'thyroid stimulating hormone deficiency', 'TSH deficiency', 'hypothalamic-pituitary hypothyroidism', 'secondary hypothyroidism']",,,226298,,,C113144,,,,,,
mondo:0016411,hypothyroidism due to deficient transcription factors involved in pituitary development or function,,,,226307,CN201345,,,,,,,,
mondo:0016412,peripheral hypothyroidism,,,,226310,,,,,,,,,
mondo:0016413,congenital hypothyroidism due to maternal intake of antithyroid drugs,,,,226313,,,,,,,,,
mondo:0016414,"hypotrichosis-intellectual disability, Lopes type",['Lopes-Marques de Faria syndrome'],,,2266,CN201347,,,,,,,,
mondo:0016416,diphallia,['Diphallus'],,,227,,,,,,752.69,,,
mondo:0016417,congenital ichthyosis-microcephalus-tetraplegia syndrome,['congenital ichthyosis-microcephalus-quadriplegia syndrome'],,,2271,,,,,,,,,
mondo:0016418,"multiple system atrophy, cerebellar type","['MSA, cerebellar type', 'MSA-c', 'sporadic olivopontocerebellar atrophy type 1', 'sporadic OPCA type 1']",,,227510,CN201371,,,,,,,,
mondo:0016419,hereditary breast carcinoma,"['breast cancer, early-onset, susceptibility to, autosomal dominant, somatic mutation', 'breast cancer susceptibility, autosomal dominant, somatic mutation', 'breast cancer, lobular, somatic', 'breast cancer, somatic', 'breast cancer, familial Male', 'breast cancer, male, susceptibility to, autosomal dominant, somatic mutation', 'breast cancer, protection against, autosomal dominant, somatic mutation', 'breast cancer, susceptibility to, autosomal dominant, somatic mutation', 'familial breast cancer', 'familial breast carcinoma', 'familial cancer of breast', 'breast cancer, familial', 'hereditary breast cancer', 'familial cancer of the breast', 'breast cancer, invasive ductal, autosomal dominant, somatic mutation', 'hereditary breast carcinoma']",,114480,227535,C0346153,"['0.2141', '0.02187', '-0.4604', '-0.03345', '0.1545', '-0.463', '0.1564', '0.03638', '-0.2122', '-0.257', '0.2467', '0.13', '-0.2008', '0.1968', '0.06445', '-0.3174', '0.04465', '-0.1984', '0.10895', '-0.144', '-0.2002', '-0.194', '0.545', '-0.1416', '0.3352', '-0.05865', '-0.1642', '-0.2747', '0.1353', '-0.439', '0.733', '-0.2852', '0.3289', '-0.0895', '0.1862', '-0.1581', '-0.634', '0.1721', '-0.0359', '0.006077', '0.3228', '-0.3684', '-0.0845', '-0.4473', '0.3677', '-0.3428', '-0.1544', '-0.12115', '-0.1141', '0.1057', '0.1642', '0.318', '-0.3704', '0.3406', '-0.2842', '0.1359', '0.2605', '-0.08575', '-0.1242', '0.3638', '0.3794', '0.2422', '0.06836', '0.289', '0.1936', '0.5044', '0.09717', '0.528', '-0.1418', '0.4094', '0.374', '-0.2465', '0.1648', '-0.1387', '0.4587', '0.0933', '-0.1057', '-0.1082', '-0.08655', '-0.2737', '-0.3113', '0.2844', '-0.02426', '-0.0941', '-0.677', '-0.374', '0.3298', '-0.2162', '0.3467', '0.2081', '0.0468', '0.2084', '-0.3606', '-0.2554', '0.631', '-0.11743', '0.1698', '-0.2145', '-0.3428', '-0.014175']",C4503,,C562840,,C50.6,,
mondo:0016420,familial flecked retinopathy,['hereditary flecked retinopathy'],,,227786,CN226924,,,,,,H35.5,,
mondo:0016421,toxic oil syndrome,,,,227972,,,,,,,,10051222,
mondo:0016422,autoimmune polyendocrinopathy type 3,"['PAS3', 'polyglandular autoimmune syndrome type 3', 'APS type 3', 'autoimmune polyendocrine syndrome type 3', 'autoimmune polyglandular syndrome type 3', 'APS3']",,,227982,C3266027,,,,,258.1,,,
mondo:0016423,autoimmune polyendocrinopathy type 4,"['autoimmune polyglandular syndrome type 4', 'APS type 4', 'autoimmune polyendocrine syndrome type 4', 'APS4']",,,227990,CN201378,,,,,258.1,,,
mondo:0016424,progressive sensorineural hearing loss-hypertrophic cardiomyopathy syndrome,"['progressive sensorineural deafness-hypertrophic cardiomyopathy syndrome', 'progressive neurosensory hearing loss-hypertrophic cardiomyopathy syndrome', 'progressive neurosensory deafness-hypertrophic cardiomyopathy syndrome']",,,228012,CN201381,,,,,,,,
mondo:0016425,Hughes-Stovin syndrome,,,,228116,CN201382,,,,,,,,
mondo:0016426,fusariosis,"['Fusarium infection', 'Fusarium caused disease or disorder']",0050289,,228119,,,,1001795,D060585,,,10051919,
mondo:0016428,multiple sclerosis variant,,,,228145,,,,,,,,,
mondo:0016429,Marburg acute multiple sclerosis,"['acute multiple sclerosis, Marburg type', 'acute multiple sclerosis, Marburg variant']",,,228157,,,,,,,,,
mondo:0016430,Balo concentric sclerosis,"['Balo concentric sclerosis', 'Baló concentric sclerosis', 'Balo^s disease', 'Tumefactive multiple sclerosis', 'encephalitis periaxialis concentrica', 'Balo disease', 'concentric demyelination', 'Balo^s concentric sclerosis', 'diffuse cerebral sclerosis of Schilder', 'Marburg variant']",0060215,,228165,C0205710,,C35257,,,341.1,,10010252,
mondo:0016431,autosomal dominant Charcot-Marie-Tooth disease type 2M,['CMT2M'],,,228179,CN201389,"['-0.04642', '0.1866', '0.06177', '0.1868', '0.2793', '-0.1841', '-0.0975', '0.588', '-0.807', '-0.379', '-0.03004', '0.2913', '-0.332', '0.5146', '-0.3618', '-0.0455', '-0.3687', '-0.731', '-0.4875', '-0.643', '0.0856', '0.513', '0.003145', '0.4248', '0.2727', '0.4053', '0.01378', '0.3313', '0.2128', '-0.0676', '-0.06866', '-0.577', '-0.0293', '0.3254', '0.2688', '-0.4917', '-0.545', '-0.1486', '0.3604', '-0.00571', '-1.449', '0.010155', '-0.3145', '0.5283', '-0.2499', '-0.3745', '0.2627', '0.1405', '-0.2396', '-0.1357', '0.4563', '0.0696', '0.09924', '-1.146', '0.4646', '-0.1891', '0.2252', '0.1498', '-0.678', '-0.4773', '-0.425', '0.2874', '1.029', '0.735', '-0.4382', '1.043', '0.12305', '1.069', '-0.4495', '0.439', '-0.994', '0.1761', '0.501', '-0.558', '1.24', '0.351', '-0.1549', '-0.01512', '0.1942', '-0.2283', '0.00206', '-0.09454', '0.6826', '0.592', '0.08887', '0.0005345', '0.1924', '0.6997', '0.747', '0.4072', '0.1947', '0.2205', '0.4478', '0.3271', '0.3306', '0.369', '0.862', '-0.5244', '0.03668', '0.63']",,,,,,,
mondo:0016432,heart-hand syndrome,['atriodigital dysplasia'],,,228184,CN201390,,,,,,,,
mondo:0016433,dysmorphism-short stature-deafness-disorder of sex development syndrome,['Dysmorphism-short stature-deafness-pseudohermaphroditism syndrome'],,,2282,CN201392,,,,,,,,
mondo:0016434,acquired dermis elastic tissue disorder,['acquired dermis elastic tissue disorder'],,,228218,CN226927,,,,,,,,
mondo:0016437,late-onset focal dermal elastosis,"['PXE-like late-onset focal dermal elastosis', 'pseudoxanthoma-like late-onset focal dermal elastosis']",,,228227,,,,,,,,,
mondo:0016438,linear focal dermal elastosis,"['Elastotic striae', 'linear focal elastosis']",,,228236,,,,,,,,,
mondo:0016439,elastoderma,,,,228240,C0406555,,,,,701.8,,,
mondo:0016440,elastofibroma dorsi,['Elastofibroma'],,,228243,CN226932,,C4245,,,,,,
mondo:0016441,acquired pseudoxanthoma elasticum,"['localized acquired cutaneous pseudoxanthoma elasticum', 'acquired Gronblad-Strandberg-Touraine syndrome', 'acquired pseudoxanthoma elasticum', 'acquired pseudoxanthoma elasticum (inherited or acquired)', 'localised acquired cutaneous pseudoxanthoma elasticum', 'acquired PXE']",,,228247,C1274759,,,,,757.39,,,
mondo:0016442,elastoma,"['juvenile elastoma without osteopoikilosis', 'Nevus elasticus', 'Weidman juvenile elastoma']",,,228254,C0473583,,,,,215.9,,,
mondo:0016443,papular elastorrhexis,"['eruptive collagenoma', 'disseminated nevus anelasticus', 'Nevus anelasticus']",,,228264,C0473584,,C4707,,,,,,
mondo:0016444,primary anetoderma,['primary macular atrophy'],,,228272,C0406550,,,,D057088,,,,
mondo:0016445,familial anetoderma,"['hereditary anetoderma', 'hereditary macular atrophy']",,,228277,CN226934,,,,,,,,
mondo:0016446,acquired cutis laxa,"['acquired cutis laxa', 'cutis laxa acquisita']",,,228285,C0406549,,,,,,,,
mondo:0016447,white fibrous papulosis of the neck,,,,228290,CN226935,,,,,,,,
mondo:0016448,pseudoxanthoma elasticum-like papillary dermal elastolysis,['PXE-like papillary dermal elastolysis'],,,228293,,,,,,,,,
mondo:0016449,mid-dermal elastolysis,,,,228299,,,,,,,,,
mondo:0016450,"autoimmune hemolytic anemia, cold type","['cold AIHA', 'cAIHA', 'cAHA']",,,228312,CN201401,,,,,,,,
mondo:0016451,idiopathic hypersomnia with long sleep time,,,,228315,C2711059,,,,,327.11,G47.11,,
mondo:0016452,idiopathic hypersomnia without long sleep time,,,,228318,C1561855,,,,,327.12,G47.12,,
mondo:0016453,foodborne botulism,['intoxication botulism'],0050352,,228371,C1739094,,C128341,,,005.1,,,
mondo:0016454,Charcot-Marie-Tooth disease type 2B5,"['SEOAN due to NEFL deficiency', 'Charcot-Marie-Tooth disease type 2B5', 'severe early-onset axonal neuropathy due to light neurofilament subunit deficiency', 'AR-CMT2B5', 'autosomal recessive Charcot-Marie-Tooth disease type 2B5']",,,228374,,,,,,,,,
mondo:0016455,virus-associated trichodysplasia spinulosa,"['Cyclosporine-induced folliculodystrophy', 'VATS', 'pilomatrix dysplasia', 'TS', 'trichodysplasia spinulosa']",,,228379,C3267126,,,,,,,,
mondo:0016456,5q14.3 microdeletion syndrome,"['chromosome 5q14.3 deletion syndrome', 'autosomal dominant intellectual disability 20', 'monosomy 5q14.3', '5q14.3 deletion syndrome', 'Del(5)(q14.3)']",,,228384,,,,,,,,,
mondo:0016457,ptosis-upper ocular movement limitation-absence of lacrimal punctum syndrome,,,,228396,CN201421,,,,,,,,
mondo:0016458,8q12 microduplication syndrome,"['chromosome 8q12 microduplication syndrome', 'trisomy 8q12', 'dup(8)(q12)']",,,228399,CN201422,,,,,,,,
mondo:0016459,2q23.1 microdeletion syndrome,"['monosomy 2q23.1', 'pseudo-Angelman syndrome', 'chromosome 2q23.1 microdeletion syndrome', 'Del(2)(q23.1)']",,,228402,,,,,,,,,
mondo:0016460,polyvalvular heart disease syndrome,['PHD syndrome'],,,228410,CN201425,,,,,,,,
mondo:0016461,5q35 microduplication syndrome,"['dup(5)(q35)', 'trisomy 5q35']",,,228415,CN201426,,,,,,,,
mondo:0016462,isolated agammaglobulinemia,"['isolated hypogammaglobulinemia', 'nonsyndromic agammaglobulinemia']",,,229717,,"['0.085', '0.3057', '-0.3953', '-0.5576', '0.4578', '-0.1661', '0.2161', '0.3738', '0.005558', '0.0359', '-0.01393', '0.046', '-0.9', '0.5044', '0.151', '0.4033', '0.0912', '-0.02107', '-0.436', '-0.485', '-0.671', '0.0978', '1.076', '-0.43', '0.09863', '0.1265', '-0.1631', '-0.212', '0.1631', '-0.8813', '-0.04453', '0.2415', '0.2576', '-0.329', '0.136', '-0.08734', '-1.067', '-0.1696', '-0.863', '-0.09344', '-0.2124', '-0.5103', '0.5977', '-0.3792', '-0.0473', '-0.4949', '-0.1575', '-0.07135', '0.02391', '-0.064', '0.3704', '-0.582', '-0.0284', '0.03976', '-0.1859', '-0.0704', '0.5693', '-0.2878', '-0.0771', '0.3254', '0.0458', '0.427', '0.258', '0.08685', '0.6216', '0.0762', '-0.1868', '0.2874', '-0.3179', '0.629', '-0.912', '-0.2435', '0.02116', '-0.351', '0.51', '-0.05374', '0.2576', '-0.239', '0.2268', '0.05923', '0.2854', '-0.2', '0.125', '0.159', '0.4043', '-0.1597', '0.7246', '0.2247', '-0.10425', '0.05093', '-0.1409', '0.5854', '-0.2578', '0.2935', '1.127', '0.9033', '0.4175', '-0.3997', '-0.05283', '-0.519']",,,,,,,
mondo:0016463,syndromic agammaglobulinemia,"['syndrome associated with agammaglobulinemia', 'hypogammaglobulinemia', 'syndromic agammaglobulinemia']",,,229720,CN226939,,C26931,,,,,,
mondo:0016464,insulin-resistance syndrome type B,['insulin-resistance type B'],,,2298,C0342337,,,,,,,,
mondo:0016466,asbestosis,"['asbestosis', 'asbestos pneumoconiosis', 'asbestos intoxination', 'asbestos intoxication', 'pulmonary fibrosis - from asbestos exposure', 'asbestos dust pneumoconiosis', 'idiopathic interstitial pneumonitis - from asbestos exposure']",10320,,2302,C0003949,,C84573,0007153,D001195,501,,,
mondo:0016467,isotretinoin syndrome,"['retinoic acid embryopathy', 'Accutane fetal effects of', 'Isotretinoin fetal effects of', 'foetal retinoid syndrome', 'Accutane foetal effects of', 'foetal isotretinoin syndrome', 'Isotretinoin teratogen syndrome', 'Retinoids embryopathy', 'Isotretinoin embryopathy', 'Accutane-exposed pregnancies', 'Isotretinoin (RoAccutane) embryopathy', 'Acutane embryopathy', 'Isotretinoin foetal effects of', 'fetal retinoid syndrome', 'fetal isotretinoin syndrome']",,,2305,,,C98929,,C535670,,,,
mondo:0016468,toxin-mediated infectious botulism,['toxin-mediated infective botulism'],,,230800,,,,,,,,,
mondo:0016469,"Ehlers-Danlos syndrome, vascular-like type","['EDS, vascular-like type']",,,230845,CN201458,,,,,,,,
mondo:0016470,Ehlers-Danlos/osteogenesis imperfecta syndrome,['EDS/OI syndrome'],,,230857,CN201460,,,,C565178,,,,
mondo:0016471,pachyonychia congenita,"['pachyonychia congenita, Jadassohn-Lewandowsky type', 'PC', 'Jackson-Lawler type pachyonychia congenita', 'pachyonychia congenita type 1', 'pachyonychia congenita syndrome', 'Jadassohn-Lewandowsky syndrome', 'congenital pachyonychia']",0050449,,2309,C0265334,"['0.0523', '-0.3486', '-0.222', '-0.1732', '0.2637', '-0.6226', '0.01851', '0.7593', '-0.4097', '0.007195', '-0.03534', '-0.0859', '-0.2042', '0.1137', '0.1635', '0.543', '0.2712', '-0.6772', '-0.1997', '-0.777', '-0.46', '-0.355', '0.413', '0.1714', '0.4583', '0.1501', '0.03244', '0.4258', '-0.0724', '-0.71', '0.3625', '-0.5312', '-0.6245', '0.3435', '0.1199', '0.09735', '-0.1438', '-0.2634', '-0.1068', '-0.05096', '-0.1876', '-0.1902', '-0.1011', '-0.2053', '0.6455', '0.559', '-0.1844', '0.2072', '0.0982', '-0.4116', '-0.3684', '0.003897', '-0.0568', '0.04733', '-0.4336', '-0.3032', '0.2372', '0.3232', '-0.871', '-0.4868', '0.12396', '0.3098', '-0.4478', '-0.00778', '-0.07367', '0.4348', '0.501', '0.429', '0.4424', '0.861', '-0.1697', '-0.584', '0.3118', '0.5127', '0.7124', '0.1597', '0.1686', '0.01944', '-0.2966', '-0.2227', '0.2491', '0.5073', '-0.1415', '-0.1526', '0.0891', '0.3499', '-0.11017', '0.0694', '0.8955', '0.11896', '0.1181', '-0.1967', '-0.1798', '0.3274', '0.268', '-0.1772', '0.1265', '-0.0691', '0.2445', '0.278']",C84986,,D053549,,,,
mondo:0016472,dracunculiasis,"['infection by Dracunculus medinensis', 'medinensis', 'Dracunculosis', 'Medina worm disease', 'Guinea worm disease', 'Dracunculus medinensis caused disease or disorder', 'parasitic infection caused by Dracunculus medinensis', 'dracontiasis', 'Guinea worm infection', 'GWD']",14418,,231,C0013100,,C84677,0007241,D004320,125.7,B72,10013618,
mondo:0016473,familial rhabdoid tumor,"['hereditary rhabdoid tumour', 'hereditary rhabdoid tumor', 'rhabdoid tumour predisposition syndrome', 'familial posterior fossa brain tumor syndrome of infancy', 'rhabdoid predisposition syndrome', 'familial posterior fossa brain tumour syndrome of infancy', 'rhabdoid tumor predisposition syndrome', 'RTPS']",,,231108,CN201468,"['0.2585', '0.3877', '-0.8594', '0.1375', '0.11334', '-0.391', '0.2235', '0.2913', '-0.3152', '-0.6157', '0.3904', '-0.04007', '-0.2712', '-0.0702', '-0.171', '-0.1506', '-0.0704', '-0.8555', '-0.1539', '-0.2408', '0.1636', '-0.2676', '0.2932', '-0.2832', '0.1362', '-0.324', '-0.1642', '0.01805', '-0.107', '-0.1147', '0.485', '-0.5166', '0.2068', '0.09766', '0.0457', '0.3872', '-0.575', '0.02515', '-0.1476', '0.2915', '-0.004738', '-0.3064', '0.304', '-0.39', '0.0342', '0.1359', '0.0314', '-0.1687', '0.3801', '0.06964', '0.211', '0.041', '-0.418', '-0.1079', '-0.1722', '0.3235', '0.2485', '0.2173', '-0.1948', '0.7515', '0.3945', '0.1932', '-0.0815', '0.266', '-0.4807', '0.3958', '0.3894', '0.521', '-0.1627', '0.8223', '0.2384', '0.2079', '0.0849', '0.147', '0.05505', '-0.03757', '-0.1887', '0.7217', '-0.592', '-0.4146', '-0.5493', '0.1012', '0.01894', '0.2078', '-0.524', '-0.679', '0.688', '-0.02135', '0.1445', '0.2422', '0.3003', '0.03317', '0.10187', '-0.516', '0.4114', '0.03717', '0.4849', '-0.717', '0.04855', '-0.0484']",C93268,,,,,,
mondo:0016474,drug-induced lupus erythematosus,"['drug-induced lupus', 'DILE', 'drug induced lupus', 'DIL', 'drug induced lupus erythematosus']",0040093,,231111,C0263591,,C114354,,,,,10013706,
mondo:0016475,Beckwith-Wiedemann syndrome due to imprinting defect of 11p15,['Beckwith-Wiedemann syndrome due to imprinting defect of type 11p15'],,,231117,CN201470,,,,,,,,
mondo:0016476,Beckwith-Wiedemann syndrome due to CDKN1C mutation,,,,231120,CN201471,,,,,,,,
mondo:0016477,Beckwith-Wiedemann syndrome due to 11p15 microdeletion,,,,231127,CN201472,,,,,,,,
mondo:0016478,Beckwith-Wiedemann syndrome due to 11p15 translocation/inversion,,,,231130,CN201473,,,,,,,,
mondo:0016479,silver-Russell syndrome due to 7p11.2p13 microduplication,"['Silver-Russell syndrome due to dup(7)(p11.2p13)', 'Silver-Russell syndrome due to trisomy 7p11.2-p13', 'Silver-Russell syndrome due to 7p11.2-p13 microduplication', 'Silver-Russell syndrome due to trisomy 7p11.2p13']",,,231137,CN201474,,,,,,,,
mondo:0016480,silver-Russell syndrome due to an imprinting defect of 11p15,['Silver-Russell syndrome due to an imprinting defect of type 11p15'],,,231140,CN201475,,,,,,,,
mondo:0016481,silver-Russell syndrome due to 11p15 microduplication,,,,231144,CN201476,,,,,,,,
mondo:0016482,silver-Russell syndrome due to maternal uniparental disomy of chromosome 11,"['Silver-Russell syndrome due to maternal uniparental disomy of chromosome type 11', 'UPD(11)mat']",,,231147,CN201477,,,,,,,,
mondo:0016483,intracranial berry aneurysm,"['familial aneurysmal subarachnoid hemorrhage', 'familial berry aneurysm', 'aneurysm, intracranial berry', 'saccular cerebral aneurysm', 'familial aneurysmal subarachnoid haemorrhage', 'familial cerebral saccular aneurysm', 'familial intracranial saccular aneurysm']",0060228,,231160,CN230268,,,,,,,,0007029
mondo:0016484,Usher syndrome type 2,['USH2'],0110827,,231178,C0339534,"['-0.414', '-0.0909', '0.1417', '0.0338', '0.2166', '-0.4543', '-0.0645', '0.643', '-0.2793', '-0.1392', '0.1178', '0.04636', '-0.06464', '0.0653', '-0.2642', '-0.4866', '0.6006', '-0.1562', '0.08246', '-0.1987', '-0.0716', '-0.1885', '-0.1814', '0.428', '0.2235', '0.1592', '-0.3574', '-0.1575', '-0.06573', '0.3062', '0.3645', '0.06396', '0.275', '0.536', '-0.1142', '-0.3003', '-0.1699', '-0.424', '-0.0965', '-0.3667', '-0.1456', '0.0909', '0.05862', '-0.2328', '-0.4001', '0.1459', '0.1627', '-0.094', '-0.1011', '0.3267', '0.1937', '0.4512', '0.2612', '-0.697', '0.02388', '0.268', '0.3792', '-0.2878', '-0.2986', '-0.05222', '-0.04184', '-0.03342', '0.2125', '0.1921', '-0.2952', '-0.1167', '-0.00889', '0.6694', '-0.3335', '0.576', '-0.3818', '0.1704', '0.1528', '-0.548', '0.5', '-0.5127', '0.2183', '0.2372', '-0.01515', '-0.12317', '0.04913', '-0.4727', '0.0189', '0.9976', '-0.534', '-0.2444', '-0.03662', '0.2087', '0.1754', '0.2408', '0.08453', '0.4814', '0.2683', '0.1729', '0.3586', '0.01001', '0.2844', '-0.9316', '0.05942', '0.2673']",C126328,,,,H35.5,,
mondo:0016485,Usher syndrome type 3,['USH3'],0110828,,231183,C1568248,,C126329,,,,H35.5,,
mondo:0016486,beta-thalassemia major,"['Cooley^s Anemia', 'Cooley anaemia', 'Beta thalassemia Major', 'Mediterranean anemia', 'Mediterranean anaemia', 'Cooley anemia', 'Cooley^s Anaemia']",0080771,,231214,,"['-0.3865', '0.3284', '-0.0869', '-0.558', '0.057', '-0.2234', '-0.7827', '1.328', '-0.8726', '-0.5996', '-0.4128', '-0.3584', '0.1427', '0.4116', '-0.491', '0.05557', '-1.144', '-0.09076', '-0.549', '-0.6465', '-0.42', '-0.3271', '0.9897', '-0.3892', '0.4978', '0.06256', '0.4487', '-0.1581', '0.3599', '-0.6914', '0.04352', '-0.031', '-0.06824', '-0.578', '-0.567', '-0.1852', '-0.5933', '-0.1554', '-0.4355', '-0.7427', '0.08167', '0.2686', '0.4001', '-0.01703', '-0.6953', '-0.4275', '-0.721', '-0.6787', '0.3025', '-0.7305', '0.1395', '-0.4702', '0.4297', '0.2375', '-0.02647', '0.02373', '-0.2173', '0.593', '-0.288', '0.4304', '-0.1716', '-0.0828', '-0.1873', '-0.289', '-0.1948', '0.1608', '0.1707', '0.8735', '-0.9688', '0.699', '0.08453', '0.2798', '0.04077', '-0.2737', '0.3599', '0.2247', '-0.01604', '-0.06934', '-0.1151', '0.2534', '-0.2151', '-0.55', '0.0649', '-0.1119', '-0.4138', '0.271', '0.4646', '0.212', '0.12177', '0.1384', '0.242', '-0.10864', '-0.12244', '-0.3718', '0.681', '0.3926', '-0.666', '-0.0866', '0.04013', '-0.611']",C129699,,,282.49,,,
mondo:0016487,beta-thalassemia intermedia,,0080772,,231222,,"['-0.1438', '0.2311', '0.04108', '-0.5723', '-0.11755', '-0.3203', '-0.636', '1.3', '-0.91', '-0.4585', '-0.3208', '0.0769', '0.1078', '0.5757', '-0.371', '-0.184', '-1.527', '-0.463', '-0.602', '-0.708', '-0.3208', '-0.2286', '0.798', '-0.608', '0.598', '-0.2028', '0.6646', '-0.2333', '0.4397', '-0.563', '0.04797', '-0.09357', '-0.2325', '-0.577', '-0.3433', '-0.68', '-0.5503', '-0.2142', '-0.0878', '-0.747', '-0.01889', '0.476', '0.669', '-0.1614', '-0.692', '-0.3755', '-0.5586', '-0.7676', '0.1547', '-0.658', '0.2148', '-0.693', '0.1917', '0.05063', '-0.2114', '0.2096', '-0.3826', '0.5635', '0.0905', '0.4175', '-0.5156', '0.002407', '-0.147', '-0.3345', '-0.03018', '0.3718', '0.219', '0.666', '-0.7144', '0.5293', '0.006283', '0.0819', '-0.2683', '-0.1646', '0.1943', '0.469', '0.1089', '-0.258', '-0.0385', '0.2507', '-0.395', '-0.933', '0.005596', '-0.3176', '-0.5986', '-0.03534', '0.4817', '0.10895', '-0.0729', '0.255', '0.4143', '0.07275', '-0.2073', '-0.2458', '0.6567', '0.2094', '-0.2969', '-0.245', '-0.1302', '-0.522']",,,,282.49,,10062923,
mondo:0016489,delta-beta-thalassemia,,0080773,141749,231237,,,C172823,,C562716,282.49,D56.2,10012236,
mondo:0016490,hemoglobin C-beta-thalassemia syndrome,"['HBC-beta-thalassemia syndrome', 'C-beta-thalassemia']",,,231242,CN201488,,,,,,,,
mondo:0016491,hemoglobin E-beta-thalassemia syndrome,"['E-beta-thalassemia', 'HbE-beta-thalassemia syndrome']",,,231249,C0472777,,,,,,,,
mondo:0016493,variant of Guillain-Barre syndrome,"['variant of GBS', 'variant of Guillain-Barré syndrome']",,,231413,CN201495,,,,,,,,
mondo:0016494,regional variant of Guillain-Barre syndrome,"['regional variant of GBS', 'regional variant of Guillain-Barré syndrome']",,,231416,CN201496,,,,,,,,
mondo:0016495,functional variant of Guillain-Barre syndrome,"['functional variant of Guillain-Barré syndrome', 'functional variant of GBS']",,,231419,CN201497,,,,,,,,
mondo:0016496,pharyngeal-cervical-brachial variant of Guillain-Barre syndrome,"['PCB variant of GBS', 'pharyngo-cervico-brachial variant of GBS', 'pharyngeal-cervical-brachial variant of Guillain-Barré syndrome', 'pharyngo-cervico-brachial variant of Guillain-BarrC) syndrome', 'pharyngo-cervico-brachial variant of Guillain-Barré syndrome', 'PCB variant of Guillain-BarrC) syndrome', 'PCB variant of Guillain-Barré syndrome', 'pharyngeal-cervical-brachial weakness']",,,231426,CN201499,,,,,,,,
mondo:0016497,paraparetic variant of Guillain-Barre syndrome,"['paraparetic variant of GBS', 'paraparetic variant of Guillain-Barré syndrome']",,,231445,CN201500,,,,,,,,
mondo:0016498,acute pure sensory neuropathy,"['acute pure sensory Guillain-Barré syndrome', 'acute pure sensory Guillain-BarrC) syndrome', 'acute pure sensory GBS']",,,231450,CN201501,,,,,,,,
mondo:0016499,acute pandysautonomia,"['acute panautonomic neuropathy', 'acute panautonomic Guillain-BarrC) syndrome', 'acute panautonomic GBS', 'acute panautonomic Guillain-Barré syndrome']",,,231457,C2315246,,,,,,,,
mondo:0016500,acute sensory ataxic neuropathy,"['acute sensory ataxic Guillain-BarrC) syndrome', 'acute sensory ataxic Guillain-Barré syndrome', 'ASAN', 'acute sensory ataxic GBS']",,,231466,CN201503,,,,,,,,
mondo:0016501,Hermansky-Pudlak syndrome with pulmonary fibrosis,['HPS with pulmonary fibrosis'],,,231500,CN201506,"['0.1462', '-0.3708', '-0.6797', '0.217', '-0.09247', '-0.1464', '0.3088', '0.3188', '-0.1207', '0.0529', '0.203', '-0.2347', '-0.5664', '0.454', '-0.5576', '-1.202', '0.1628', '0.2401', '0.3672', '-0.5845', '-0.4607', '-0.391', '0.642', '-0.993', '-0.10986', '-0.2183', '0.2932', '0.752', '0.4917', '0.2632', '0.604', '-0.2805', '0.9404', '-0.02106', '0.4822', '-0.188', '-0.1632', '-0.3174', '0.1986', '0.683', '0.1753', '-0.4448', '-0.518', '-0.3284', '0.2379', '-0.09705', '0.1925', '0.2047', '0.3164', '-0.3403', '-0.1422', '-0.2357', '0.5264', '-0.2275', '0.3728', '0.4736', '-0.4558', '0.5596', '-0.6445', '-0.5254', '-0.5337', '-0.1372', '0.2332', '0.11487', '-0.504', '-0.3806', '0.2417', '0.1824', '-0.631', '0.5327', '-0.702', '-0.607', '0.5127', '-0.3691', '0.08826', '0.4924', '0.753', '-0.08014', '0.3528', '-0.1606', '-0.374', '-0.2158', '0.02135', '0.2406', '0.273', '0.5005', '0.0994', '0.523', '0.2081', '-0.05936', '0.5605', '-0.0721', '-0.3188', '0.2854', '0.8115', '0.0796', '0.0005713', '0.1087', '-0.3726', '-0.10785']",,,,,E70.3,,
mondo:0016502,Hermansky-Pudlak syndrome without pulmonary fibrosis,['HPS without pulmonary fibrosis'],,,231512,CN201507,"['0.2886', '-0.529', '-0.6216', '0.2424', '-0.01846', '-0.2172', '0.37', '0.3137', '-0.1888', '-0.05066', '0.2086', '-0.3364', '-0.6455', '0.4492', '-0.831', '-1.082', '0.1073', '0.05453', '0.07074', '-0.5024', '-0.3616', '-0.137', '0.741', '-1.064', '-0.1252', '-0.2527', '0.353', '0.7036', '0.528', '0.3335', '0.536', '-0.198', '1.082', '-0.1486', '0.438', '-0.04636', '-0.5015', '-0.4475', '0.1865', '0.544', '0.404', '-0.4043', '-0.578', '-0.263', '0.1589', '0.0933', '0.206', '0.1483', '0.2493', '-0.4272', '-0.1776', '-0.2551', '0.477', '-0.4153', '0.258', '0.346', '-0.4602', '0.5684', '-0.6074', '-0.514', '-0.3599', '-0.05893', '0.3093', '0.0569', '-0.634', '-0.4946', '0.03693', '0.1575', '-0.704', '0.5405', '-0.5757', '-0.579', '0.5146', '-0.5947', '0.1155', '0.413', '0.7197', '0.01614', '0.5005', '-0.1643', '-0.4304', '-0.26', '0.1565', '0.1816', '0.2217', '0.6', '-0.1218', '0.7124', '0.2632', '-0.07355', '0.72', '-0.2014', '-0.3926', '0.3066', '0.931', '-0.03534', '-0.0733', '0.2842', '-0.2974', '-0.0259']",,,,,E70.3,,
mondo:0016503,congenital erosive and vesicular dermatosis,"['congenital erosive and vesicular dermatosis with reticulated supple scarring', 'CEVD']",,,231573,,,,,,,,,
mondo:0016504,primary unilateral adrenal hyperplasia,['PUAH'],,,231580,C4274967,,,,,,,,
mondo:0016505,aldosterone-producing adrenal cortex adenoma,"['aldosterone-producing adrenal cortex adenoma', 'APAC', 'Pure APAC', 'aldosterone producing adrenal cortex adenoma', 'Pure aldosterone-producing adrenocortical carcinoma', 'aldosterone producing adrenal cortical adenoma', 'adrenocortical carcinoma with pure aldosterone hypersecretion', 'Pure aldosterone-secreting adrenocortical carcinoma']",,,231625,CN226945,,C48451,1000015,D018246,,,10056950,
mondo:0016506,ectopic aldosterone-producing tumor,"['Extra-adrenal aldosterone-producing tumor', 'Extra-adrenal aldosterone-producing tumour']",,,231632,CN201515,,,,,,,,
mondo:0016509,microcornea-posterior megalolenticonus-persistent fetal vasculature-coloboma syndrome,"['MPPC syndrome', 'microcornea posterior megalolenticonus persistent fetal vasculature coloboma', 'microcornea posterior megalolenticonus persistent foetal vasculature coloboma']",,,231736,CN201521,,,,,,,,
mondo:0016510,epibulbar lipodermoid-preauricular appendage-polythelia syndrome,,,,231742,CN226948,,,,,,,,
mondo:0016511,infectious embryofetopathy,,,,232035,,,,,,,,,
mondo:0016512,Kabuki syndrome,"['KMS', 'NKS', 'Kabuki make up syndrome', 'Kabuki make-up syndrome', 'Niikawa-Kuroki syndrome']",0060473,,2322,C0796004,"['0.2412', '-0.2786', '0.555', '-0.0923', '0.699', '0.396', '0.2185', '0.9272', '-1.452', '-0.826', '0.2125', '-0.05634', '0.5356', '-0.014404', '-0.0161', '0.0582', '-0.0517', '-0.13', '-0.1558', '-0.4482', '0.3318', '0.371', '0.167', '0.03726', '0.1167', '-0.4172', '-0.2798', '-0.4097', '0.3716', '-0.01743', '0.5776', '0.1893', '0.1462', '-0.0805', '0.254', '-0.4448', '-0.361', '-0.2341', '-0.513', '-0.647', '-0.002989', '0.3042', '-0.06476', '-0.1123', '0.1891', '-0.1747', '-0.3408', '-0.03708', '0.2788', '0.299', '-0.799', '-0.2837', '-0.1068', '0.07446', '-0.6553', '-0.02625', '0.4885', '-0.0978', '0.2666', '0.26', '-0.1114', '0.431', '0.07', '0.3987', '0.612', '-0.05655', '0.3362', '0.1748', '-0.622', '-0.09766', '0.0673', '0.1256', '-0.7134', '0.2966', '0.058', '0.03842', '0.3704', '-0.5933', '-0.06122', '-0.007698', '0.2074', '-0.0005383', '-0.2666', '0.741', '-0.05133', '0.346', '-0.263', '-0.3096', '0.09174', '0.2306', '-0.287', '0.3623', '-0.3823', '0.2214', '0.772', '-0.0963', '0.2722', '-0.4534', '0.8696', '-0.0949']",C124837,,C537705,,,10063935,
mondo:0016513,alpha-thalassemia-related diseases,,,,232288,CN201534,,,,,,D56.0,,
mondo:0016514,epidermolysis bullosa simplex with anodontia/hypodontia,"['Gamborg-Nielsen syndrome', 'Kallin syndrome']",,,2325,,,,,,,,,
mondo:0016515,Kallmann syndrome-heart disease syndrome,,,,2326,CN201538,,,,,,,,
mondo:0016516,Kenny-Caffey syndrome,['Kenny syndrome'],0080724,,2333,C0265291,"['-0.4983', '0.2327', '0.574', '-0.6235', '0.295', '0.1315', '-0.0971', '0.2737', '-0.3762', '-0.5615', '-0.3196', '0.02869', '-0.2913', '-0.2295', '-0.2397', '-0.1803', '0.571', '-0.1945', '-0.004463', '-0.76', '0.1244', '-0.1932', '0.2048', '-0.0449', '0.08325', '0.1938', '-0.2974', '0.3926', '0.548', '-0.2052', '-0.2393', '-0.04837', '0.2343', '-0.11365', '-0.1415', '-0.09015', '-0.0669', '-0.04987', '0.122', '-0.256', '0.336', '0.0767', '0.2244', '-0.1755', '0.10767', '-0.5293', '0.2073', '0.1906', '0.3662', '-0.2242', '0.2917', '0.226', '0.3135', '-0.1714', '-0.4265', '-0.724', '0.1974', '0.2996', '-0.0922', '0.1368', '0.3115', '-0.14', '-0.309', '-0.2166', '0.3577', '0.0791', '0.1432', '0.808', '-0.4443', '0.2401', '-0.588', '0.1083', '0.465', '-0.3887', '-0.3003', '0.05017', '0.451', '0.2222', '0.1481', '0.2932', '-0.02895', '0.315', '-0.05286', '0.1732', '-0.176', '0.1359', '0.014206', '-0.008415', '0.4243', '0.4326', '-0.337', '0.4412', '0.1448', '-0.1893', '1.061', '0.2625', '0.3757', '0.224', '0.434', '0.2169']",C130991,,C537020,759.89,,,
mondo:0016518,isolated punctate palmoplantar keratoderma,"['isolated punctate palmoplantar hyperkeratosis', 'isolated punctate PPK', 'nonsyndromic punctate palmoplantar keratoderma']",,,2338,,,,,,,,,
mondo:0016520,isolated Klippel-Feil syndrome,"['Klippel-Feil sequence', 'Klippel-Feil malformation', 'congenital fused cervical segments', 'congenital cervical vertebral fusion', 'nonsyndromic Klippel-Feil syndrome']",,,2345,,"['-0.1766', '0.02219', '-0.6025', '-0.462', '-0.07654', '-0.0918', '0.756', '0.5215', '-0.684', '0.2', '-0.421', '0.09454', '0.2942', '0.569', '-0.0436', '0.1954', '0.549', '-0.855', '-0.4424', '-0.4758', '-0.2158', '-0.2406', '0.6196', '-0.6387', '0.05106', '0.01823', '0.4312', '0.2798', '-0.0118', '0.1655', '0.4482', '0.2747', '0.3433', '0.01674', '-0.09753', '-0.2886', '0.5146', '-0.5186', '0.4417', '-0.4282', '-0.01313', '-0.068', '0.5854', '-0.3037', '0.212', '-0.2659', '0.1876', '-0.3882', '0.0206', '0.4204', '0.00679', '-0.2363', '0.3706', '0.12054', '-0.3982', '-0.3032', '0.3215', '0.006996', '0.7134', '0.06055', '0.2208', '0.07477', '-0.849', '0.05148', '-0.001288', '0.51', '0.4214', '0.4526', '-0.2151', '0.2532', '-0.687', '0.7856', '0.2654', '-0.292', '0.4197', '0.08234', '0.5938', '0.248', '-0.5054', '-0.331', '-0.3884', '0.0882', '0.327', '0.7393', '-0.1835', '0.1953', '0.04056', '0.714', '0.1267', '-0.6035', '-0.1014', '0.1714', '-0.02109', '-0.1267', '0.511', '-1.208', '0.3525', '-0.748', '0.5327', '-0.454']",,,,,,,
mondo:0016521,muscular pseudohypertrophy-hypothyroidism syndrome,"['Hoffman syndrome', 'Kocher-Debre-Semelaigne syndrome', 'Kocher-Debré-Semelaigne syndrome']",,,2349,,,,,,,,,
mondo:0016522,Kousseff syndrome,"['sacral meningocele, conotruncal heart defects, and minor anomalies of head and neck', 'sacral meningocele conotruncal heart defects', 'sacral meningocele-conotruncal heart defects syndrome']",,,2351,C2931444,,,,C537223,,,,
mondo:0016523,bronchogenic cyst,"['bronchogenic cyst', 'bronchogenic cyst (disease)']",,,2357,,,,,D001994,,,10064585,0100730
mondo:0016524,congenital vascular bone syndrome,,,,235832,,,,,,,,,
mondo:0016525,familial hyperaldosteronism,"['hereditary hyperaldosteronism', 'FH', 'genetic hyperaldosteronism']",,,371861,CN229602,"['-0.553', '0.554', '-0.0698', '-0.3162', '-0.2666', '0.09515', '-0.2666', '-0.1121', '-0.438', '0.1425', '-0.4856', '-0.327', '0.146', '0.1733', '-0.3916', '-0.3906', '-0.1462', '0.0467', '0.562', '-0.4277', '-0.1627', '-0.3945', '0.585', '-0.3083', '0.3735', '0.4373', '0.1595', '-0.3745', '0.1978', '-0.6323', '-0.2401', '0.4937', '0.888', '0.19', '-0.2457', '-0.7026', '-0.8975', '0.1495', '-0.3967', '-0.4092', '0.159', '-0.827', '0.4263', '-0.6904', '0.5835', '-0.0010195', '0.2443', '0.2676', '0.436', '0.11725', '0.0606', '-0.398', '0.4395', '-0.3296', '-0.5464', '0.1686', '0.2444', '-0.7476', '-0.3413', '0.5815', '-0.443', '-0.1433', '0.004333', '-0.821', '-0.521', '-0.1399', '0.1716', '0.343', '-0.7217', '0.04855', '-0.2522', '-0.2426', '0.4753', '-0.656', '0.4214', '0.287', '-0.708', '0.2477', '-0.2268', '0.013596', '0.2932', '0.113', '-0.3276', '-0.2229', '0.2317', '0.2942', '0.2656', '-0.01201', '0.763', '-0.0935', '0.0753', '0.3076', '0.3374', '-0.3047', '1.229', '0.1252', '0.4736', '-0.1285', '-0.4136', '0.083']",C127160,,C580087,,E26.0,,
mondo:0016526,trisomy 9p,"['partial trisomy of chromosome 9p', 'partial trisomy of the short arm of chromosome type 9', 'partial duplication of chromosome 9p', 'Duplication 9p', 'chromosome 9p duplication', '9p duplication', 'Duplication of the short arm of chromosome 9', '9p trisomy', 'trisomy type 9p', 'partial trisomy of the short arm of chromosome 9', 'partial duplication of the short arm of chromosome 9', 'trisomy of the short arm of chromosome 9', 'partial trisomy 9p']",,,262767,C0265428,,,,,,,,
mondo:0016527,glycogen storage disease due to lactate dehydrogenase deficiency,"['LDH deficiency', 'lactate dehydrogenase deficiency', 'glycogenosis due to lactate dehydrogenase deficiency', 'GSD due to lactate dehydrogenase deficiency']",,,2364,,"['-0.1445', '0.1797', '0.04236', '0.07227', '0.05972', '-0.1545', '-0.01865', '0.1526', '-0.04517', '-0.0311', '-0.02654', '0.006466', '-0.007763', '-0.02565', '-0.03494', '-0.08954', '-0.02719', '-0.05804', '-0.2375', '-0.2646', '0.05856', '-0.1562', '0.209', '0.01738', '-0.1003', '-0.0994', '0.03473', '-0.02692', '-0.07355', '-0.0758', '0.1537', '0.04742', '0.1633', '0.07794', '-0.03622', '-0.1526', '-0.006535', '-0.04562', '-0.0275', '-0.0908', '-0.001554', '-0.2279', '0.0818', '0.0621', '-0.1273', '-0.0725', '0.09424', '0.11383', '-0.04526', '0.1654', '-0.0772', '-0.0707', '0.04996', '0.001477', '-0.10205', '-0.10626', '0.1624', '-0.11884', '-0.1666', '0.03513', '0.164', '0.02771', '0.1268', '-0.0646', '0.005745', '0.02509', '0.1671', '0.06204', '-0.2444', '0.0835', '-0.1578', '0.01869', '-0.00558', '-0.03653', '0.1067', '0.1367', '0.08655', '0.02794', '-0.1506', '-0.045', '-0.04855', '0.02417', '-0.0627', '0.0513', '0.1039', '0.06726', '0.11194', '0.06335', '0.3052', '0.01366', '0.1476', '0.1078', '-0.04443', '-0.04617', '0.363', '0.1874', '0.1392', '-0.1416', '-0.004635', '0.09686']",,,C580233,,,,
mondo:0016528,limb body wall complex,"['body stalk anomaly', 'umbilical cord, short', 'Cyllosomas', 'limb-body wall complex', 'short umbilical cord syndrome', 'aplasia of the cord', 'LBWC syndrome']",,,2369,CN201594,,,,,,,,
mondo:0016529,duplication of urethra,['urethral duplication'],,,237,,,,,,753.8,,,
mondo:0016530,laryngocele,,,,2372,C0265761,,C97062,,D059608,748.3,Q31.3,10023885,
mondo:0016531,digestive duplication,,,,238,,,,,,,,,
mondo:0016532,Lennox-Gastaut syndrome,"['macrocephaly and epileptic encephalopathy', 'LGS', 'epileptic encephalopathy Lennox-Gastaut type', 'Lennox syndrome', 'encephalopathy of childhood']",0050561,606369,2382,C0238111,"['0.5674', '0.4202', '-0.2808', '-0.1302', '-0.4722', '-0.2015', '1.05', '1.437', '-0.2397', '-0.4116', '-0.84', '-0.03333', '0.1171', '0.3618', '-0.1798', '-0.3352', '-0.1812', '-0.141', '0.1849', '-0.44', '0.4736', '0.4429', '0.5474', '-0.4963', '0.26', '-0.11224', '-0.1385', '-0.645', '-0.8984', '0.403', '0.3157', '0.11395', '0.2874', '0.4333', '-0.1858', '-0.2051', '0.3518', '-0.6846', '0.0897', '-0.1921', '-0.0728', '-0.71', '-0.276', '-0.05222', '0.5366', '-0.01624', '0.00779', '0.3474', '0.005066', '0.583', '-0.1858', '0.8833', '0.2311', '-0.3276', '-0.1215', '0.2595', '0.2203', '-0.2002', '0.0954', '-0.001285', '0.2751', '0.1101', '0.1477', '-0.01688', '-0.3684', '-0.0715', '0.01009', '-0.03802', '0.3027', '0.5156', '0.6836', '0.2883', '-0.065', '0.1428', '0.2727', '0.7817', '-0.0707', '-0.452', '-0.5054', '0.1459', '0.1443', '-0.0364', '-0.2463', '0.4236', '0.366', '-0.2693', '0.4036', '0.2686', '0.729', '0.4634', '0.1367', '-0.001306', '-0.10455', '0.4355', '-0.05838', '0.3386', '0.6753', '-0.265', '0.0922', '-0.3623']",C84816,,D065768,,,10048816,
mondo:0016533,apolipoprotein A-II amyloidosis,"['AApoAII amyloidosis', 'hereditary amyloid nephropathy due to apolipoprotein A-II variant', 'hereditary renal amyloidosis due to apolipoprotein A-II variant', 'familial renal amyloidosis due to apolipoprotein A-II variant', 'familial amyloid nephropathy due to apolipoprotein A-II variant']",,,238269,CN201610,,,,,,,,
mondo:0016534,infundibulo-neurohypophysitis,,,,238305,,,,,,,,,
mondo:0016535,hypohidrotic ectodermal dysplasia,"['anhidrotic ectodermal dysplasia', 'ectodermal dysplasia, hypohidrotic', 'ectodermal dysplasia 1, Anhydrotic', 'CST syndrome', 'hypohidrotic X-linked ectodermal dysplasia', 'ectodermal dysplasia anhidrotic', 'EDA', 'anhidrotic ectodermal dysplasia 1', 'anhidrotic ectodermal dysplasia 3', 'HED']",14793,,238468,,"['0.4907', '0.1622', '0.374', '-0.56', '0.6313', '-0.0008554', '-0.4482', '0.725', '-0.04932', '-0.4524', '-0.1667', '-0.2788', '-0.0659', '0.348', '-0.11456', '0.01317', '0.005272', '-0.2394', '-0.2123', '-0.589', '-1.102', '-0.317', '0.966', '-0.1155', '0.04572', '-0.0793', '-0.371', '-0.4045', '-0.09406', '-1.191', '0.3264', '0.693', '0.1174', '0.1251', '0.3074', '0.402', '0.0724', '-0.1022', '-0.2142', '-0.624', '0.1814', '0.1137', '0.03857', '-0.532', '0.3274', '-0.656', '-0.5757', '-0.4202', '0.7266', '0.2026', '0.152', '-0.4673', '0.468', '-0.2067', '0.2578', '-0.4385', '0.643', '-0.1637', '0.1558', '-0.783', '-0.4395', '0.6797', '-0.7134', '0.2556', '0.4622', '0.2043', '0.0652', '-0.2313', '0.2747', '0.6167', '-0.7305', '0.1838', '-0.3914', '0.2593', '0.4768', '0.2944', '0.3171', '-0.4062', '-0.0838', '-0.2996', '-0.0446', '0.1781', '0.406', '0.2725', '0.01122', '0.2847', '-0.1492', '0.05432', '0.0382', '0.38', '-0.04974', '0.2646', '0.2512', '0.4497', '0.518', '0.154', '-0.0491', '-0.3564', '0.0969', '1.001']",C84562,,,,,,0007607
mondo:0016536,autosomal recessive lymphoproliferative disease,['CD27 deficiency'],,,238505,,"['0.0824', '0.0979', '0.1036', '-0.6567', '-0.0753', '-0.3738', '0.2074', '-0.3608', '0.131', '-0.1898', '0.02184', '0.005283', '-0.1432', '-0.32', '-0.1401', '-0.2003', '-0.1713', '0.0834', '-0.02475', '-0.683', '-0.02708', '-0.5747', '0.3442', '-0.3494', '0.1558', '-0.06244', '-0.1836', '-0.3022', '-0.04166', '-0.858', '0.2908', '0.394', '0.55', '0.2578', '0.3162', '0.0789', '-0.7456', '-0.2313', '-0.3042', '-0.5244', '-0.52', '-0.0702', '0.2472', '-0.189', '-0.1927', '-0.6816', '-0.276', '0.0205', '0.1786', '0.2249', '0.0999', '0.3945', '0.444', '0.177', '-0.2483', '-0.2377', '-0.01778', '-0.2542', '-0.604', '0.01206', '0.2112', '0.266', '-0.02939', '-0.03546', '0.594', '-0.162', '0.4443', '0.2644', '-0.01052', '0.9126', '-0.4946', '-0.3713', '-0.2747', '-0.02657', '0.2278', '-0.01026', '0.13', '0.02759', '0.2817', '-0.1256', '-0.3494', '-0.0516', '-0.0776', '0.1466', '-0.1677', '-0.10754', '0.3677', '0.1857', '0.05768', '-0.05112', '0.4207', '-0.1272', '0.2664', '-0.2086', '0.7007', '0.811', '0.1891', '-0.1201', '-0.2051', '0.006695']",,,,,,,
mondo:0016537,lymphoproliferative syndrome,"['lymphoproliferative disorder', 'lymphoproliferative syndrome']",0060704,,238510,CN201619,,C9308,,D008232,,,,
mondo:0016539,atypical hypotonia-cystinuria syndrome,['atypical HCS'],,,238523,CN201620,"['-0.1825', '0.4236', '0.353', '-0.452', '0.1565', '-0.707', '0.0005817', '0.4888', '-0.2527', '0.1257', '-0.3943', '-0.003622', '0.2886', '-0.2544', '-0.0703', '-0.0637', '0.2164', '-0.11053', '0.02187', '-0.641', '0.02722', '0.07275', '0.4114', '-0.2039', '0.08325', '0.06305', '-0.245', '-0.3894', '0.2153', '-0.189', '0.3418', '0.3594', '0.6636', '0.4329', '-0.338', '-0.0731', '-0.337', '-0.172', '-0.4182', '-0.184', '0.264', '-0.4902', '-0.1758', '0.1038', '-0.2776', '-0.178', '-0.2113', '0.139', '-0.2766', '0.08594', '-0.2125', '-0.04288', '-0.2832', '-0.371', '-0.3076', '-0.1306', '0.0572', '-0.1693', '-0.0426', '0.4822', '-0.1714', '-0.1486', '-0.0651', '0.0681', '0.279', '0.0698', '0.1917', '-0.0614', '-0.4587', '0.3293', '-0.3025', '0.2208', '0.1848', '-0.6196', '0.02524', '-0.12366', '0.01604', '-0.2247', '-0.3276', '0.168', '0.284', '0.1469', '-0.4385', '0.1875', '-0.03296', '0.3901', '0.1808', '0.6694', '0.6323', '0.0724', '0.291', '0.6714', '0.2683', '-0.0584', '0.3958', '0.2146', '0.11206', '-0.4326', '0.4336', '0.1115']",,,,,,,
mondo:0016540,congenital secondary polycythemia,['congenital secondary erythrocytosis'],,,238536,,,,,,,,,
mondo:0016541,acquired secondary polycythemia,"['acquired secondary polycythemia', 'acquired secondary erythrocytosis']",,,238547,,,,,,,,,
mondo:0016542,immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections syndrome,"['IL10-related early-onset IBD', 'autosomal recessive early-onset IBD', 'IL10-related early-onset inflammatory bowel disease', 'autosomal recessive early-onset inflammatory bowel disease']",,,238569,CN201623,"['0.2625', '0.1084', '0.1398', '-0.1473', '0.584', '-0.7935', '0.4727', '-0.04443', '-0.678', '0.1466', '0.4055', '0.1104', '-0.007587', '0.801', '-0.0973', '-0.0137', '0.2988', '0.3142', '-0.3853', '-0.3345', '0.1729', '0.04922', '0.225', '-0.002474', '-0.1704', '0.3423', '-0.3152', '0.056', '0.07733', '-0.1683', '0.3704', '-0.2043', '0.4502', '0.10956', '1.108', '0.266', '-1.046', '0.1414', '0.495', '0.287', '-0.12463', '-0.257', '-0.576', '0.7773', '0.1625', '0.339', '-0.3208', '-0.6724', '0.4243', '0.198', '-0.4658', '-0.07544', '0.648', '0.5557', '-0.03958', '-0.911', '-0.768', '0.1209', '-0.581', '-0.9688', '0.6807', '0.12036', '-0.4404', '0.03397', '0.1236', '0.1829', '0.03876', '0.8364', '-0.327', '0.2837', '0.0751', '-0.0891', '-0.1913', '-0.4958', '-0.253', '0.675', '0.05124', '1.288', '-0.2166', '-0.11786', '-0.5933', '0.014465', '-0.3972', '0.3494', '-0.0913', '0.1699', '0.1656', '0.4224', '0.4902', '0.3933', '-0.133', '0.4722', '-0.2333', '0.495', '0.4084', '0.4941', '0.719', '-0.6284', '-0.413', '-0.2605']",,,,,,,
mondo:0016543,hyperphenylalaninemia due to tetrahydrobiopterin deficiency,"['hyperphenylalaninemia due to BH4 deficiency', 'hyperphenylalaninemia', 'hyperphenylalaninemia due to tetrahydrobiopterin deficiency', 'non-phenylketonuric hyperphenylalaninemia']",,,238583,C0751435,"['-0.1146', '0.3337', '0.2197', '-0.6304', '0.2563', '-0.505', '-0.3008', '0.4346', '-0.0783', '0.0842', '-0.303', '-0.3455', '0.3367', '0.2815', '0.08057', '-0.2925', '-3.69e-05', '-0.5547', '0.08466', '-0.802', '0.2585', '-0.575', '0.385', '-0.11334', '-0.1261', '-0.1177', '0.10394', '-0.1697', '-0.1682', '-0.1339', '0.1273', '0.256', '0.2133', '0.1501', '-0.378', '0.303', '-0.3564', '-0.05386', '-0.02946', '0.03787', '0.6353', '-0.5547', '0.177', '-0.348', '0.1024', '-0.4856', '0.405', '-0.3706', '-0.2786', '1.093', '0.04214', '0.1807', '-0.1943', '-0.561', '-0.2517', '-0.0824', '0.139', '0.3418', '-0.6147', '0.6475', '-0.2983', '-0.185', '0.662', '0.02028', '-0.1447', '0.475', '0.461', '0.1586', '-0.244', '0.3425', '-0.2136', '-0.3066', '0.09735', '0.01903', '0.2117', '0.3228', '0.1094', '-0.3845', '-0.3022', '-0.626', '-0.4402', '0.2301', '0.005547', '0.08014', '0.2495', '0.0607', '0.3132', '-0.2705', '0.635', '0.17', '0.6357', '0.5967', '0.2834', '-0.3687', '0.155', '0.4578', '0.03763', '0.11615', '0.3574', '-0.464']",,,,,,,
mondo:0016544,IgG4-related mesenteritis,"['liposclerotic mesenteritis', 'sclerosing mesenteritis', 'mesenteric lipogranuloma', 'mesenteric panniculitis', 'isolated mesenteric lipodystrophy', 'lipomatous mesenteritis']",,,238593,,,,,,,,,
mondo:0016545,leukoencephalopathy-palmoplantar keratoderma syndrome,['leukoencephalopathy palmoplantar keratoderma'],,,2386,CN201627,,,,,,,,
mondo:0016546,primary orthostatic tremor,"['orthostatic tremor, primary', 'shaky leg syndrome', 'pot', 'OT']",,,238606,,,,,C536418,,,,
mondo:0016547,Beckwith-Wiedemann syndrome due to NSD1 mutation,,,,238613,CN201629,,,,,,,,
mondo:0016548,megacystis-megaureter syndrome,['megaureter-megacystis syndrome'],,,238637,,,,,,,,,
mondo:0016549,"primary megaureter, adult-onset form",,,,238642,CN201632,,,,,,,,
mondo:0016550,"congenital primary megaureter, obstructed form",,,,238646,,,,,,,,,
mondo:0016551,"congenital primary megaureter, refluxing form",,,,238650,,,,,,,,,
mondo:0016552,"congenital primary megaureter, nonrefluxing and unobstructed form",,,,238654,,,,,,,,,
mondo:0016553,isolated congenital hypogonadotropic hypogonadism,['nonsyndromic congenital hypogonadotropic hypogonadism'],,,238666,CN924907,,,,,,E23.0,,
mondo:0016554,neonatal iodine exposure,['iodine antenatal exposure'],,,238688,CN226956,,,,,,,,
mondo:0016555,transient congenital hypothyroidism due to maternal factor,,,,238696,,,,,,,,,
mondo:0016556,transient congenital hypothyroidism due to neonatal factor,,,,238699,,,,,,,,,
mondo:0016557,leukonychia totalis,"['hereditary white nails', 'total leukonychia']",,,2387,,,,,C535889,,,,
mondo:0016558,familial congenital mirror movements,"['familial congenital mirror movements', 'congenital mirror movements', 'familial congenital controlateral synkinesia', 'hereditary congenital controlateral synkinesia', 'isolated congenital mirror movements', 'congenital mirror movement disorder', 'CMM', 'hereditary congenital mirror movements', 'bimanual synkinesis', 'isolated congenital controlateral synkinesia']",0111153,,238722,,"['-0.481', '0.3394', '-0.2776', '0.2255', '-0.2632', '-0.5103', '-0.062', '-0.01979', '-0.4197', '-0.4565', '-0.1151', '-0.0676', '0.458', '0.6562', '-0.10876', '0.2096', '-0.01833', '-0.0402', '0.00808', '-1.124', '-0.3193', '0.1372', '0.344', '-0.2578', '0.227', '0.2798', '-0.2905', '0.6724', '-0.0665', '0.1327', '-0.0858', '-0.1389', '-0.11694', '0.01656', '0.1305', '-0.009254', '-0.1218', '-0.2988', '0.03223', '-0.1654', '0.217', '0.0771', '-0.544', '0.2876', '0.4685', '-0.09247', '0.03046', '0.1802', '-0.1412', '0.3086', '-0.65', '0.2766', '0.0723', '-0.4202', '0.02664', '-0.622', '0.2397', '0.2449', '0.03102', '-0.0491', '0.06192', '0.2856', '0.4302', '-0.2373', '-0.6694', '0.3652', '0.725', '0.147', '-0.288', '0.2134', '0.1793', '-0.0784', '0.1412', '-0.04742', '-0.02621', '0.2935', '-0.3518', '0.369', '-0.2289', '-0.2622', '0.1556', '-0.01268', '0.528', '0.42', '0.11237', '-0.664', '0.1225', '-0.05005', '0.174', '0.1443', '-0.1887', '-0.1338', '0.1433', '0.1765', '0.7236', '0.1907', '0.1404', '-0.5938', '0.344', '0.3608']",,,,,,,
mondo:0016559,glaucoma secondary to spherophakia/ectopia lentis and megalocornea,['megalocornea-spherophakia-secondary glaucoma syndrome'],,,238763,CN201642,"['0.3699', '-0.132', '-0.6685', '1.092', '-0.12067', '0.1384', '0.0581', '1.079', '-0.0767', '-0.847', '0.4443', '-0.2932', '-0.06134', '0.961', '-1.002', '-0.1565', '-0.1241', '-0.2036', '0.269', '-0.578', '0.1713', '0.5674', '0.007553', '-0.0927', '0.05298', '-0.2031', '-0.08777', '0.5356', '-0.1681', '0.1583', '0.2512', '-0.133', '0.694', '0.10596', '-0.196', '0.1688', '-0.2568', '-0.6777', '0.3745', '-0.4885', '0.602', '-0.672', '0.497', '-0.2632', '-0.4146', '0.9336', '0.2305', '0.0367', '0.788', '-0.3738', '-0.01608', '0.001804', '-0.6816', '-1.541', '0.5674', '-0.2123', '0.36', '0.368', '-1.306', '-0.612', '-0.292', '-0.176', '0.0469', '0.5293', '-0.618', '-0.4775', '0.4202', '0.694', '-0.2842', '0.819', '0.1006', '0.959', '0.595', '-0.58', '-0.354', '-0.03738', '0.5024', '0.8', '-0.1403', '0.469', '0.2317', '-0.2095', '-0.357', '0.879', '0.1448', '0.06573', '0.261', '-0.01675', '0.3845', '0.578', '-0.009636', '0.3433', '-0.788', '0.2654', '1.336', '-0.4197', '-0.04843', '0.02008', '-0.0595', '-0.2817']",,,,,,,
mondo:0016560,ptosis-syndactyly-learning difficulties syndrome,,,,238766,CN201643,,,,,,,,
mondo:0016561,1q44 microdeletion syndrome,"['chromosome 1q44 microdeletion syndrome', 'Del(1)(q44)', 'monosomy 1q44']",,,238769,CN201644,,,,,,,,
mondo:0016562,progressive supranuclear palsy-pure akinesia with gait freezing syndrome,"['PSP-pure akinesia with gait freezing', 'PSP-PAGF']",,,240094,CN226961,,,,,,,,
mondo:0016563,progressive supranuclear palsy-corticobasal syndrome,"['PSP-corticobasal syndrome', 'PSP-CBS']",,,240103,CN201681,,,,,,,,
mondo:0016564,progressive supranuclear palsy-progressive non-fluent aphasia syndrome,"['progressive supranuclear palsy-apraxia of speech syndrome', 'PSP-PNFA', 'PSP-AOS']",,,240112,CN226962,,,,,,,,
mondo:0016565,syndromic genetic obesity,"['syndrome associated with obesity (disease)', 'syndromic obesity (disease)']",,,240371,CN226963,,,,,,,,
mondo:0016566,loiasis,"['African eye worm', 'Loa loa filariasis']",13523,,2404,C0023968,,C34784,1000729,D008118,125.2,B74.3,10024797,
mondo:0016567,locked-in syndrome,"['Cerebromedullospinal disconnection', 'locked in syndrome', 'locked-in state']",12697,,2406,,,,,D011782,344.81,,10024792,
mondo:0016568,Lowe-Kohn-Cohen syndrome,"['Lowe Kohn Cohen syndrome', 'deafness-nephritis-ano-rectal malformation syndrome', 'dominant ano-rectal malformation, nephritis and nerve-deafness', 'deafness - nephritis - ano-rectal malformation', 'deafness nephritis anorectal malformation']",,,2408,C2931080,,,,C535996,,,,
mondo:0016570,primary pulmonary lymphoma,,,,2420,C4273669,,,,,,,10037418,
mondo:0016571,macrocephaly-short stature-paraplegia syndrome,['Volcke-Soekarman syndrome'],,,2427,,,,,C537718,,,,
mondo:0016572,central bilateral macrogyria,,,,2431,C4303949,,,,,,,,
mondo:0016573,acute fatty liver of pregnancy,"['AFLP', 'acute fatty liver, gestational']",,,243367,C1455728,,,,C537957,,,10000746,
mondo:0016574,hypo- and hypermelanotic cutaneous macules-retarded growth-intellectual disability syndrome,"['congenital hypomelanotic and hypermelanotic macules', 'hereditary congenital hypopigmented and hyperpigmented macules', 'Westerhof-Beemer-Cormane syndrome', 'macules, hereditary congenital hypopigmented and hyperpigmented', 'macules hereditary congenital hypopigmented and hyperpigmented', 'Westerhof Beemer Cormane syndrome']",,154000,2435,C1835172,,,,C537836,,,,
mondo:0016575,primary ciliary dyskinesia,"['Dextrocardia bronchiectasis and sinusitis', 'Primary ciliary dyskinesia and situs inversus', 'ciliary dyskinesia primary', 'Kartagener syndrome', 'Primary ciliary dyskinesia, Kartagener type', 'Siewert syndrome', 'Kartagener^s syndrome', 'bronchiectasis, chronic sinusitis and dextrocardia syndrome', 'ICS', 'PCD', 'immotile ciliary syndrome', 'ciliary motility disorder', 'Immotile cilia syndrome, Kartagener type', 'Dextrocardia-bronchiectasis-sinusitis syndrome']",9562,,244,C0008780,"['-0.001768', '0.1501', '0.1058', '-0.51', '-0.1268', '-0.3645', '0.7104', '0.565', '-0.068', '-0.7974', '0.389', '-0.776', '0.12244', '0.1694', '0.06616', '-0.1354', '-0.4202', '0.0865', '-0.623', '-0.63', '-0.4487', '-0.0815', '0.4844', '-0.71', '0.2764', '-0.02238', '-0.2142', '0.305', '0.1952', '-0.2869', '0.5073', '0.289', '-0.06198', '-0.097', '0.2067', '-0.1842', '0.03738', '-0.7227', '-0.1262', '0.3088', '-0.1537', '0.08844', '-0.11945', '0.1174', '-0.2034', '0.1521', '-0.1573', '-0.2128', '0.4263', '0.661', '-0.4546', '0.012215', '-0.1388', '-0.4844', '-0.21', '-0.6445', '0.5234', '-0.27', '-0.165', '-0.03976', '0.801', '0.8525', '0.09033', '0.5903', '-0.0701', '-0.6533', '0.6016', '0.241', '0.0199', '0.2668', '-0.01941', '-0.1371', '-0.587', '-0.00841', '0.05194', '-0.2228', '0.4768', '-0.3079', '-0.636', '0.39', '-0.1082', '0.2598', '0.2262', '0.2184', '-0.035', '0.09564', '0.03302', '-0.2482', '-0.4402', '-0.11993', '0.4004', '0.1644', '-0.10565', '0.3936', '0.7495', '0.2329', '-0.0753', '-0.4888', '-0.412', '0.4963']",C84797,,D007619,,,10069713,
mondo:0016576,split hand-foot malformation,"['split hand foot malformation', 'ectrodactyly', 'split-hand deformity', 'SHFM', 'split hand-split foot malformation', 'lobster-claw deformity', 'split-hand/foot malformation', 'FEWER digits', 'isolated split hand-split foot malformation']",0090020,,2440,C0265554,"['0.1455', '0.3774', '-0.1908', '0.03766', '0.4211', '-0.0951', '-0.034', '0.2812', '-0.1747', '-0.6816', '-0.1687', '-0.01306', '-0.1875', '0.4277', '0.1407', '-0.05502', '0.4106', '-0.3235', '-0.03354', '-0.472', '-0.436', '0.4873', '0.632', '-0.1722', '0.2212', '0.04214', '-0.2893', '0.2279', '0.33', '-0.5493', '0.3413', '-0.651', '-0.031', '0.3772', '-0.09204', '-0.2384', '-0.1716', '-0.02539', '-0.376', '-0.4392', '-0.3208', '-0.0998', '-0.1752', '-0.6567', '0.213', '-0.7393', '-0.11786', '0.1774', '-0.1038', '-0.1666', '-0.004818', '0.06235', '-0.2773', '-0.1001', '-0.3723', '-0.5874', '0.3215', '-0.05475', '-0.1192', '-0.2031', '-0.2358', '-0.297', '0.1422', '0.355', '-0.7427', '0.594', '0.282', '0.4336', '-0.1783', '-0.0761', '-0.6597', '0.2546', '0.4822', '0.289', '0.3586', '0.2856', '-0.1033', '0.05133', '-0.1101', '-0.625', '-0.5483', '-0.09216', '0.4421', '0.5684', '0.5034', '-0.2076', '-0.2734', '0.409', '-0.33', '-0.1111', '0.06036', '0.4868', '-0.000583', '0.08563', '0.4778', '-0.07385', '0.4414', '-1.04', '0.451', '0.1903']",C75000,,,,,,
mondo:0016577,biliary atresia with splenic malformation syndrome,['BASM syndrome'],,,244283,CN201730,,,,,,,,
mondo:0016579,dominant hypophosphatemia with nephrolithiasis or osteoporosis,,,,244305,CN228623,"['0.36', '-0.3276', '0.1592', '0.5464', '0.2375', '-0.594', '-0.6323', '0.8594', '-0.6567', '-0.4265', '0.1925', '0.371', '-0.1133', '0.4224', '-0.4485', '-0.1855', '-0.11487', '0.608', '-0.6436', '-0.07104', '-0.254', '-0.407', '0.307', '-0.4688', '0.2688', '-0.42', '0.1718', '-0.715', '-0.645', '-0.07776', '0.5415', '-0.747', '-0.278', '-0.6284', '0.0771', '-0.3872', '-0.1808', '-0.6997', '0.01222', '-0.4727', '0.1755', '-0.11176', '0.414', '-0.349', '0.5527', '-0.7397', '0.2023', '0.1392', '0.1492', '0.758', '0.5557', '0.0518', '0.517', '-0.393', '-0.3677', '-0.6177', '-0.3232', '0.275', '-0.537', '0.02544', '0.4104', '0.1109', '-0.8716', '-0.7256', '-0.049', '0.8755', '0.5356', '0.9243', '-0.3945', '-0.5723', '0.6304', '-0.4287', '0.15', '-0.3787', '0.4175', '0.5923', '-0.2515', '0.5938', '-0.03867', '0.3098', '0.0479', '-0.349', '0.45', '0.596', '-0.5483', '0.8096', '0.2035', '-0.1388', '1.228', '0.1004', '-0.0992', '-0.3025', '-1.017', '-0.1334', '0.3796', '-0.5005', '0.1902', '-0.5234', '-0.3328', '-0.4702']",,,,,,,
mondo:0016580,congenital pulmonary airway malformation,"['congenital cystic adenomatoid malformation of lung', 'congenital cystic adenomatoid malformation', 'congenital cystic adenomatoid malformation of the lung', 'congenital cystic adenomatous malformation of the lung', 'cystic adenomatoid malformation of lung', 'CPAM', 'congenital cystic disease of the lung', 'CCAM']",,,2444,,,C98892,,D015615,,,,
mondo:0016581,conotruncal heart malformations,"['Double-outlet right ventricle', 'conotruncal anomaly face syndrome', 'persistent truncus arteriosus', 'interrupted aortic Arch', 'truncus arteriosus communis', 'conotruncal heart malformations, variable', 'Taussig-Bing syndrome or defect', 'conotruncal heart malformations', 'conotruncal cardiac defects', 'CTHM']",,217095,2445,C1857586,"['-0.2236', '0.161', '0.08954', '-0.2002', '0.507', '-0.7305', '0.2996', '0.4326', '-0.4265', '-0.64', '0.0421', '-0.936', '-0.2847', '0.0575', '-0.5063', '-0.1006', '-1.261', '-0.3625', '-0.3606', '-0.5957', '0.3032', '1.069', '0.8853', '-0.306', '0.3123', '-0.0324', '-0.2505', '0.2352', '0.5444', '0.2588', '0.8115', '-0.2269', '0.2473', '0.4692', '-0.1261', '0.02238', '-0.0292', '0.417', '0.07166', '-0.2974', '-0.0579', '0.2426', '0.1935', '0.2487', '0.3193', '-0.02625', '0.05652', '0.3018', '-0.059', '0.03415', '0.1209', '-0.2336', '-0.2247', '-0.195', '-0.04398', '-0.02606', '0.281', '0.27', '-0.287', '0.4087', '-0.0688', '0.1393', '-0.3506', '0.1897', '0.1703', '-0.01512', '0.3118', '0.1164', '-0.8096', '0.3157', '-0.09937', '-0.07776', '0.02432', '-0.01057', '-0.4324', '0.1982', '0.06476', '-0.3738', '-0.565', '-0.06094', '0.1506', '0.3918', '0.0174', '0.0172', '-0.1368', '-0.6904', '0.623', '0.03345', '-0.1431', '-0.7354', '0.2573', '0.0692', '-0.1924', '0.03537', '1.204', '0.0638', '0.3105', '-0.401', '-0.2302', '0.05026']",,,,747.11,,,
mondo:0016582,congenital mitral malformation,,,,2447,,,,,,,,,
mondo:0016583,familial intestinal malrotation-facial anomalies syndrome,"['Stalker Chitayat syndrome', 'intestinal malrotation facial anomalies familial type', 'Stalker-Chitayat syndrome']",,,2454,,,,,,,,,
mondo:0016584,mandibuloacral dysplasia,"['MAD', 'mandibuloacral dysplasia with lipodystrophy']",0081127,,2457,CN118835,"['-0.2844', '0.1194', '0.3887', '-0.3037', '0.3416', '-0.298', '-0.003492', '0.2632', '-0.1818', '0.03287', '-0.2051', '-0.06216', '-0.1678', '-0.2725', '-0.2172', '0.11786', '0.4722', '-0.172', '-0.1798', '-0.577', '-0.08417', '-0.0766', '0.2617', '-0.169', '0.001814', '0.1583', '-0.1033', '-0.1412', '-0.06354', '-0.394', '0.12274', '0.04355', '0.2769', '0.1013', '0.0788', '0.05807', '-0.0614', '-0.05844', '-0.191', '-0.2041', '0.1442', '-0.2744', '-0.05298', '-0.003696', '-0.07935', '-0.4607', '-0.015274', '0.2389', '0.06415', '-0.10114', '-0.0792', '-0.03455', '0.2986', '0.1763', '-0.3584', '-0.2058', '-0.05823', '-0.1663', '-0.5596', '-0.08435', '0.1512', '-0.03088', '-0.1561', '-0.0189', '-0.00726', '0.0765', '0.297', '0.214', '-0.10565', '0.192', '-0.2395', '-0.1002', '0.212', '0.003002', '-0.1262', '-0.213', '0.0788', '-0.0737', '-0.09375', '-0.1466', '0.09344', '0.1816', '-0.08636', '0.3157', '-0.1305', '-0.1001', '0.006702', '0.3838', '0.2003', '0.07306', '0.23', '0.4656', '0.0687', '0.1791', '0.2913', '-0.0838', '0.5386', '-0.2167', '0.4163', '0.2344']",,,,,,,
mondo:0016586,systemic mastocytosis,"['systemic tissue mast cell disease', 'systemic tissue Mast cell disease', 'systemic mastocytosis', 'Agressive systemic mastocytosis', 'systemic mast cell disease', 'systemic mastocytosis with associated hemotologic non-mast cell lineage disease (SM-AHNMD)', 'Mast cell disease', 'SMCD - systemic mast cell disease', 'SM']",349,,2467,C0221013,,C9235,,,,,10042949,
mondo:0016587,arrhythmogenic right ventricular cardiomyopathy,"['arrhythmogenic RVD', 'ARVC cardiomyopathy', 'arrhythmogenic right ventricular dysplasia/cardiomyopathy', 'arrhythmogenic right ventricular cardiomyopathy', 'right ventricular dysplasia', 'ARVC', 'ARVD', 'arrhythmogenic right ventricular dysplasia']",0050431,,247,CN239850,"['0.2698', '-0.6934', '-0.12256', '0.501', '-0.04288', '-0.6533', '0.7188', '0.724', '-0.0585', '-0.4568', '0.2076', '-0.477', '-0.416', '0.566', '-0.5767', '0.3057', '-0.811', '-0.3208', '-0.4375', '-1.019', '0.1937', '0.439', '1.021', '-0.2212', '0.3218', '-0.1631', '0.3542', '0.3682', '-0.09247', '-0.661', '0.906', '-0.2188', '0.664', '0.5854', '0.3696', '-0.4956', '0.1418', '-0.2096', '0.8647', '-0.5303', '-0.010796', '0.5166', '0.007797', '0.4143', '0.4521', '0.5615', '-0.0997', '0.52', '0.2256', '-0.6885', '-0.2795', '0.1769', '1.017', '0.05283', '0.612', '-0.562', '-0.3218', '0.1593', '-0.9434', '-0.3135', '-0.1318', '0.3787', '0.4326', '-1.3', '-0.5923', '0.2988', '0.327', '0.598', '-0.545', '-0.1102', '-0.515', '-0.0133', '0.06335', '-0.1102', '0.08044', '0.653', '-0.3748', '-0.05893', '-0.2476', '0.1791', '-0.1063', '-0.3325', '-0.007267', '-0.3557', '1.01', '-0.3477', '0.3723', '0.03558', '0.6357', '0.1992', '0.11804', '-0.1859', '-0.269', '0.501', '0.7754', '0.8496', '0.5015', '-0.4058', '-0.4111', '-0.3232']",C84571,,D019571,425.4,,10058093,
mondo:0016588,infantile mercury poisoning,"['erythroedema polyneuritis', 'infantile acrodynia', 'infantile mercury intoxication', 'Swift-Feer disease', 'pink disease', 'Feer disease', 'Swift disease']",,,247165,CN201782,,,,D000170,,,,
mondo:0016589,progressive cerebello-cerebral atrophy,['PCCA'],,,247198,,"['-0.1023', '0.0871', '-0.02278', '0.003387', '0.00487', '-0.1661', '0.007366', '0.1644', '-0.1252', '-0.0645', '-0.0472', '-0.05905', '-0.0636', '0.0289', '0.02458', '-0.06665', '0.005062', '-0.0258', '-0.0866', '-0.2576', '-0.0321', '-0.06287', '0.02443', '-0.02267', '0.0248', '-0.01645', '-0.06274', '-0.01237', '-0.0318', '-0.0529', '0.0843', '0.0278', '0.1683', '0.06775', '0.03613', '-0.04892', '-0.00513', '-0.0791', '0.04712', '-0.1276', '0.05756', '-0.136', '-0.00797', '-0.01662', '-0.03473', '-0.0948', '-0.0341', '0.05957', '-0.02293', '0.014465', '-0.01854', '0.05643', '0.0551', '-0.04138', '-0.0568', '-0.0174', '0.1077', '-0.01424', '-0.1726', '0.03117', '0.051', '0.0632', '-0.002844', '0.05408', '-0.10004', '-0.004883', '0.1658', '0.1572', '-0.0955', '0.12146', '-0.0889', '0.00549', '0.02397', '-0.1171', '0.05115', '0.02332', '0.01405', '0.02428', '-0.0327', '-0.03062', '0.02908', '0.006218', '-0.01758', '0.1377', '-0.04285', '0.01201', '0.01419', '0.1323', '0.1376', '0.010895', '0.1189', '0.09674', '-0.002132', '0.03503', '0.2305', '0.0707', '0.1852', '-0.08344', '-0.007694', '0.0632']",,,,,,,
mondo:0016591,sporadic adult-onset ataxia of unknown etiology,"['SAOA', 'idiopathic late-onset cerebellar ataxia']",,,247234,,,,,,,,,
mondo:0016592,non-hereditary degenerative ataxia,,,,247239,,,,,,,,,
mondo:0016593,acquired ataxia,['acquired ataxia'],,,247242,,,,,,,,,
mondo:0016594,superficial siderosis,"['superficial hemosiderosis of the CNS', 'superficial siderosis of the CNS', 'hemosiderosis of the central nervous system', 'superficial siderosis of the central nervous system', 'superficial hemosiderosis of the central nervous system']",,,247245,,,,,,,,,
mondo:0016595,inhalational anthrax,"['inhalation anthrax', 'pulmonary anthrax', 'respiratory anthrax disease', 'inhalation anthrax disease', 'respiratory anthrax', 'woolsorters^ disease', 'wool-sorters^ disease']",0050160,,247257,C0155866,,,,C571912,022.1,,10035667,
mondo:0016596,hyperphosphatasia-intellectual disability syndrome,"['hyperphosphatasia with intellectual disability syndrome', 'HPMR', 'Mabry syndrome', 'hyperphosphatasia with mental retardation syndrome']",,,247262,C1855923,"['-0.214', '-0.03888', '0.3813', '-0.386', '0.2874', '-0.1204', '-0.02861', '0.593', '-0.098', '-0.264', '-0.1505', '-0.11206', '-0.03305', '-0.1527', '-0.216', '0.1257', '0.10767', '-0.0307', '-0.4001', '-0.4038', '0.1421', '0.0442', '0.241', '-0.0946', '0.319', '-0.03683', '-0.05225', '-0.11755', '0.3286', '-0.255', '0.2195', '-0.03436', '0.3496', '0.274', '0.03818', '-0.2352', '-0.02055', '-0.3127', '-0.0516', '-0.1869', '0.1012', '-0.2024', '-0.01784', '-0.1693', '-0.1514', '-0.3188', '0.04932', '0.3804', '-0.2627', '0.00875', '-0.3828', '0.033', '0.02312', '-0.04794', '-0.293', '-0.1298', '-0.144', '-0.10706', '-0.183', '0.1364', '0.31', '-0.07214', '-0.1355', '-0.1359', '-0.1528', '-0.01881', '0.1193', '0.436', '-0.4507', '0.162', '-0.1697', '0.0476', '0.04932', '-0.05017', '-0.02359', '0.04257', '0.348', '-0.2878', '-0.12054', '0.00841', '0.0313', '0.2014', '-0.01161', '0.373', '0.07996', '0.138', '-0.0969', '0.3352', '0.1447', '0.1531', '0.1122', '0.415', '0.112', '0.161', '0.5264', '0.1302', '0.3784', '-0.372', '0.333', '0.2079']",,,,,,,
mondo:0016598,autosomal recessive secondary polycythemia not associated with VHL gene,"['autosomal recessive secondary polycythemia, non-Chuvash type', 'autosomal recessive secondary erythrocytosis, non-Chuvash type', 'autosomal recessive secondary erythrocytosis not associated with VHL gene']",,,247378,CN226972,,,,,,,,
mondo:0016599,autosomal dominant secondary polycythemia,"['secondary polycythemia, autosomal dominant', 'autosomal dominant secondary erythrocytosis']",,,247511,CN201790,"['-0.3347', '0.0968', '-0.0705', '-0.179', '0.2009', '0.1901', '-0.079', '0.248', '-0.06555', '0.0683', '-0.1176', '0.3193', '0.1616', '-0.1351', '0.04556', '0.01996', '0.0416', '0.2239', '-0.128', '-0.6216', '-0.1765', '-0.1945', '0.325', '-0.03955', '0.189', '-0.0407', '0.1401', '-0.2637', '-0.1757', '-0.3113', '0.4353', '-0.00884', '0.3718', '0.1354', '-0.3667', '-0.1923', '-0.4802', '-0.2805', '0.0965', '-0.6846', '0.006798', '-0.1709', '0.3828', '-0.3325', '-0.3547', '-0.666', '0.0776', '-0.1677', '0.0597', '-0.10034', '0.2135', '-0.1155', '0.1124', '-0.2085', '0.2046', '-0.2651', '0.393', '-0.239', '-0.3687', '0.0964', '0.3787', '-0.02106', '0.1893', '-0.2805', '-0.07465', '-0.00572', '0.2291', '0.3203', '-0.3457', '0.0726', '-0.1549', '-0.0989', '-0.2976', '-0.09796', '0.3054', '-0.03928', '-0.1847', '0.143', '0.1127', '-0.253', '-0.0407', '0.105', '0.3196', '0.1232', '0.005096', '0.03427', '0.06235', '-0.04138', '0.172', '-0.010994', '-0.01471', '0.1467', '-0.2751', '-0.1476', '0.68', '0.515', '0.269', '-0.3748', '-0.386', '0.0644']",,,,,,,
mondo:0016600,acute neonatal citrullinemia type I,"['classic citrullinemia type I', 'acute neonatal citrullinemia type 1', 'classic citrullinemia type 1']",,,247546,CN201793,,,,,,,,
mondo:0016601,adult-onset citrullinemia type I,"['late-onset citrullinemia type 1', 'late-onset citrullinemia type I', 'adult-onset citrullinemia type 1']",,,247573,CN201794,,,,,,,,
mondo:0016602,citrin deficiency,,,,247582,C1997910,,,,,,,,
mondo:0016603,citrullinemia type II,"['adult-onset type II citrullinemia', 'citrullinemia type II', 'CTLN2', 'citrullinemia type 2', 'adult-onset citrin deficiency', 'adult-onset type 2 citrullinemia']",,,247585,,"['-0.1569', '0.4377', '0.1917', '-0.143', '-0.10645', '-0.4988', '-0.1874', '0.2344', '-0.3098', '0.3083', '-0.4446', '-0.1442', '0.2084', '-0.2715', '0.1556', '-0.09454', '0.0886', '-0.1577', '0.03564', '-0.3237', '-0.0867', '-0.2937', '-0.0741', '-0.0861', '0.1432', '-0.04483', '0.0443', '-0.2659', '0.0124', '-0.3687', '-0.05518', '0.1625', '0.6865', '-0.282', '-0.1428', '-0.148', '-0.543', '-0.2306', '-0.1711', '-0.396', '0.3074', '-0.6265', '0.02145', '0.0858', '-0.04434', '-0.2769', '-0.2993', '0.1569', '0.03784', '0.9536', '0.2607', '0.5347', '-0.567', '-0.4668', '0.29', '-0.1973', '0.367', '-0.43', '-0.1595', '0.2102', '-0.09546', '0.5176', '0.1892', '-0.3794', '0.10785', '-0.07166', '0.4192', '-0.0596', '-0.1725', '0.0968', '-0.141', '0.4453', '-0.2299', '-0.4407', '0.51', '0.399', '0.3245', '0.1068', '-0.3176', '0.2377', '0.2954', '-0.2406', '-0.0955', '-0.332', '0.7646', '0.207', '0.2683', '0.5254', '0.575', '0.2269', '0.1678', '0.5137', '0.2028', '-0.05518', '0.538', '0.553', '0.3542', '-0.273', '0.1711', '0.3413']",C150603,,,,,,
mondo:0016604,dysraphism-cleft lip/palate-limb reduction defects syndrome,"['dysraphism, cleft lip/palate, limb reduction defects', 'Medeira-Dennis-Donnai syndrome']",,,2476,CN201798,,,,,,,,
mondo:0016605,perinatal lethal hypophosphatasia,"['perinatal lethal phosphoethanolaminuria', 'HPPN', 'perinatal lethal Rathburn disease']",,,247623,C2673477,"['-0.5586', '0.1548', '0.2534', '-0.00909', '-0.0654', '-0.216', '0.01346', '1.245', '-0.464', '-0.2808', '-0.2185', '-0.162', '-0.2886', '0.0919', '-0.1904', '0.2021', '0.27', '-0.0748', '-0.418', '-0.719', '-0.2046', '-0.659', '1.317', '-0.627', '-0.3315', '-0.1703', '-0.00337', '0.1809', '-0.3794', '0.09894', '-0.1626', '-0.05252', '-0.1367', '0.2192', '0.0872', '-0.249', '0.2015', '-0.202', '0.323', '0.0946', '-0.2301', '-0.2842', '0.2488', '-0.1932', '0.004585', '0.05063', '-0.512', '0.08246', '-0.1609', '0.7095', '-0.418', '-0.5586', '0.0445', '-0.2434', '-0.493', '-0.3281', '-0.2267', '-0.3286', '0.2059', '-0.1008', '0.4573', '0.10425', '-0.1835', '-0.03925', '-0.10187', '0.0737', '0.743', '0.2727', '-0.2695', '0.05536', '0.1202', '0.1392', '0.2742', '0.3398', '0.02945', '0.427', '0.2288', '-0.3203', '-0.3486', '-0.5537', '-0.4138', '-0.02895', '0.05984', '-0.2042', '-0.01894', '0.556', '0.305', '-0.12256', '0.422', '-0.08496', '0.1688', '-0.0638', '-0.3945', '0.3552', '-0.2372', '0.692', '0.1895', '-0.5483', '0.1243', '-0.2144']",,,,,E83.3,,
mondo:0016607,odontohypophosphatasia,['HPPO'],,,247685,C1840322,"['0.2223', '-0.3618', '0.2852', '-0.01836', '0.5596', '0.3433', '0.4556', '0.6147', '-0.462', '0.427', '-0.3872', '-0.3271', '-0.243', '0.04092', '-0.2961', '-0.2096', '0.3389', '-0.2722', '-1.392', '-0.641', '-0.2305', '-0.2246', '0.7886', '-0.0653', '0.3037', '0.2292', '-0.1497', '0.04672', '0.438', '-0.11694', '0.11786', '0.262', '-0.4817', '0.2764', '0.11206', '0.1265', '-0.3367', '-0.236', '0.566', '-0.5933', '0.787', '-0.3672', '0.248', '-0.268', '-0.02336', '-0.491', '0.1459', '-0.1741', '0.3813', '0.03506', '-0.01224', '-0.443', '-0.3643', '-0.2319', '-0.7754', '-0.08435', '0.4143', '-0.4282', '-0.238', '-0.4119', '0.68', '0.01735', '-0.1797', '-0.3262', '0.3252', '-0.1443', '0.02606', '0.3208', '0.00672', '0.006317', '-0.2429', '0.03998', '0.3564', '-0.2727', '0.3174', '0.3845', '0.625', '-0.448', '0.02155', '-0.315', '-0.2295', '-0.0221', '0.146', '0.1345', '-0.1456', '0.0573', '-0.0633', '-0.0293', '0.2166', '0.135', '-0.335', '0.1536', '-0.2673', '0.4294', '0.6284', '0.537', '0.7227', '-0.4387', '-0.0807', '-0.113']",C131309,,C564146,,E83.3,,
mondo:0016608,megalencephaly,"['megalencephaly (disease)', 'macroencephaly', 'megalencephaly']",,,2477,,,,,D058627,742.4,,10050183,0001355
mondo:0016609,inflammatory myopathy with abundant macrophages,['imam'],,,247718,CN201809,,,,,,,,
mondo:0016610,idiopathic eosinophilic myositis,['idiopathic eosinophilia-associated myopathy'],,,247724,,,,,,,,,
mondo:0016611,lipoblastoma,"['embryonic lipoma', 'foetal lipoma', 'infantile lipoma', 'fetal lipoma']",,,247762,C1260965,,C27483,,D062689,,,,
mondo:0016612,X-linked cerebellar ataxia,"['cerebellar ataxia, X-linked', 'hereditary ataxia, X-linked', 'X-linked hereditary ataxia']",0111828,,247765,,,,,,,,,
mondo:0016613,APC-related attenuated familial adenomatous polyposis,"['APC-related AFAP', 'APC-related attenuated FAP', 'APC-related attenuated familial polyposis coli']",,,247806,CN201818,,,,,,,,
mondo:0016614,autosomal recessive ataxia due to PEX10 deficiency,['mild peroxismal disorder due to PEX10 deficiency'],,,247815,CN201819,,,,,,,,
mondo:0016615,oligoarticular juvenile idiopathic arthritis with anti-nuclear antibodies,"['pauciarticular chronic arthritis with anti-nuclear antibodies', 'oligoarticular JIA with anti-nuclear antibodies']",,,247839,CN201823,,,,,,M08.4,,
mondo:0016616,oligoarticular juvenile idiopathic arthritis without anti-nuclear antibodies,"['oligoarticular JIA without anti-nuclear antibodies', 'pauciarticular chronic arthritis without anti-nuclear antibodies']",,,247846,CN201824,,,,,,M08.4,,
mondo:0016617,rheumatoid factor-negative juvenile idiopathic arthritis with anti-nuclear antibodies,"['polyarthritis without rheumatoid factor with anti-nuclear antibodies', 'juvenile rheumatoid factor-negative polyarthritis with anti-nuclear antibodies', 'rheumatoid factor-negative JIA with anti-nuclear antibodies']",,,247854,,,,,,,,,
mondo:0016618,rheumatoid factor-negative juvenile idiopathic arthritis without anti-nuclear antibodies,"['polyarthritis without rheumatoid factor without anti-nuclear antibodies', 'juvenile rheumatoid factor-negative polyarthritis without anti-nuclear antibodies', 'rheumatoid factor-negative JIA without anti-nuclear antibodies']",,,247861,,,,,,,,,
mondo:0016619,autosomal recessive hypohidrotic ectodermal dysplasia,"['hypohidrotic ectodermal dysplasia, autosomal recessive', 'hypohidrotic ectodermal dysplasia autosomal recessive', 'autosomal recessive anhidrotic ectodermal dysplasia', 'anhidrotic ectodermal dysplasia, autosomal recessive', 'AR-HED']",,,248,C0406702,"['-0.0598', '0.2903', '0.2361', '-0.1763', '0.3684', '-0.0967', '-0.2142', '0.1909', '0.001447', '-0.4204', '-0.1284', '-0.1213', '-0.3037', '0.02971', '0.03186', '0.161', '0.1284', '-0.05914', '-0.3884', '-0.3196', '-0.2593', '-0.05496', '0.3079', '0.0655', '0.09906', '0.01909', '-0.282', '0.05432', '0.1592', '-0.34', '0.1566', '0.2316', '0.03888', '0.04483', '0.0846', '-0.1323', '-0.05795', '0.02397', '0.004456', '-0.2128', '0.0892', '-0.1622', '-0.0209', '-0.2064', '-0.11053', '-0.3564', '0.0807', '-0.04968', '0.3147', '-0.1338', '0.00948', '-0.00867', '0.1531', '0.1716', '-0.2181', '-0.1935', '0.1941', '-0.05667', '-0.2764', '-0.11127', '0.1923', '0.155', '0.0605', '-0.2484', '0.1517', '0.11316', '0.257', '0.2272', '-0.3486', '0.2688', '-0.5576', '-0.07806', '0.07697', '0.06506', '0.1827', '0.1156', '0.134', '0.0709', '0.03143', '0.0475', '0.0752', '0.03717', '0.2029', '0.0449', '-0.1156', '0.08875', '0.02965', '0.1804', '0.2045', '0.2905', '0.0332', '0.3152', '0.005733', '0.1183', '0.611', '0.2295', '0.2656', '-0.2241', '0.05594', '0.592']",C84580,,D053360,,,,
mondo:0016620,primary hypertrophic osteoarthropathy,"['PDP', 'hypertrophic osteoarthropathy, primary', 'idiopathic hypertrophic osteoarthropathy', 'hypertrophic osteoarthropathy, primary, autosomal recessive, 1', 'PHO', 'hypertrophic osteoarthropathy, primary, autosomal recessive, type 1', 'hypertropic osteoarthropathy, primary', 'Touraine-Solente-Gole syndrome', 'pachydermoperiostosis of nail [ambiguous]', 'pachydermoperiostosis syndrome', 'pachydermoperiostosis', 'pachydermoperiostosis of nail', 'Touraine Solente Gole syndrome', 'PHOAR1']",14283,,2796,CN202658,"['0.01072', '-0.514', '0.08673', '-0.1399', '0.266', '-0.1001', '0.473', '0.6587', '-0.2693', '0.3337', '-0.5547', '-0.1317', '-0.1458', '-0.03677', '-0.2966', '0.1375', '0.253', '0.2428', '-0.2942', '-0.889', '0.692', '0.236', '0.5728', '-0.6636', '0.03482', '0.4922', '0.246', '-0.1552', '0.3643', '-0.616', '0.613', '0.2893', '-0.0626', '-0.05066', '-0.06494', '-0.683', '-0.1731', '-0.2705', '-0.07794', '-0.178', '0.4229', '-0.4473', '0.5435', '-0.04587', '0.8745', '-0.2173', '0.3767', '0.4526', '-0.1726', '0.1909', '-0.1937', '-0.3464', '0.338', '0.1277', '-0.3254', '-0.4912', '-0.124', '0.751', '-0.28', '-0.537', '0.3586', '0.1792', '-0.4011', '-0.561', '0.04236', '-0.282', '0.08105', '0.8135', '-0.11365', '0.5938', '-0.9272', '-0.7954', '0.4285', '0.03848', '0.767', '0.594', '-0.351', '-0.4634', '-0.3616', '-0.1029', '0.6953', '0.2308', '-0.009926', '0.261', '-0.26', '-0.07574', '0.234', '0.01991', '0.00555', '-0.00279', '0.2603', '0.12115', '0.2842', '0.6353', '0.719', '-0.05722', '0.2083', '-0.01326', '0.06537', '-0.4866']",C85023,,D010004,,,10051686,
mondo:0016621,juvenile Huntington disease,"['juvenile onset HD', 'juvenile Huntington chorea', 'Huntington disease, juvenile onset', 'JHD']",,,248111,C0751208,"['0.10315', '0.73', '0.01723', '0.151', '-0.3755', '-0.864', '0.5176', '1.071', '-0.8545', '-0.04852', '-0.1688', '-0.1912', '-0.07184', '-0.179', '0.7837', '-0.4558', '-0.3005', '-0.575', '-0.3132', '-0.85', '-0.2773', '-0.612', '0.5645', '-0.3726', '0.065', '0.10175', '-0.3394', '0.1465', '-0.4805', '0.2288', '0.4885', '0.2734', '-0.2922', '-0.3206', '-0.1516', '-0.1846', '-0.4788', '-0.708', '-0.587', '0.2844', '0.3982', '-0.603', '0.6855', '-0.0196', '1.108', '0.11316', '-0.1219', '-0.3008', '0.1554', '0.9307', '0.1112', '0.3604', '-0.4314', '-0.643', '0.6226', '-0.1821', '0.1759', '0.008804', '-0.8286', '-0.062', '0.04782', '0.2627', '0.05978', '0.1539', '-0.1066', '0.185', '0.1218', '-0.463', '0.135', '0.3884', '-0.03574', '-0.641', '0.2068', '-0.5723', '0.575', '0.693', '-0.1514', '-0.191', '-0.54', '-0.1362', '0.2983', '-0.1372', '-0.2499', '0.5522', '0.06003', '0.449', '0.2444', '0.0695', '0.3713', '0.328', '-0.0919', '-0.0196', '0.2224', '0.4888', '0.2219', '-0.1876', '0.1212', '0.02', '-0.01', '0.3284']",C147072,,,,,,
mondo:0016622,Melhem-Fahl syndrome,"['Melhem Fahl syndrome', 'fifteen dorsal vertebrae and rib pairs']",,,2482,C2931453,,,,C537238,,,,
mondo:0016624,inherited deficiency anemia,"['constitutional rare deficiency anaemia', 'constitutional rare deficiency anemia']",,,248296,,,,,,,,,
mondo:0016625,acquired deficiency anemia,"['rare acquired deficiency anaemia', 'rare acquired deficiency anemia']",,,248302,CN226976,,,,,,,,
mondo:0016630,isolated delta-storage pool disease,"['isolated dense-SPD', 'isolated dense-storage pool disease', 'isolated delta-SPD']",,,248340,CN201837,,,,,,,,
mondo:0016638,familial hypodysfibrinogenemia,,,,248408,CN201839,"['-0.02591', '0.0351', '0.00452', '-0.01643', '0.001563', '-0.05634', '0.00607', '0.0645', '-0.06274', '-0.0002421', '0.001497', '-0.01636', '-0.02357', '0.01866', '-0.03165', '-0.04828', '-0.01208', '-0.01749', '0.0152', '-0.0932', '0.002256', '-0.02628', '0.03424', '-0.01936', '0.01143', '-0.005108', '0.01646', '-0.00916', '0.01253', '-0.03067', '0.0632', '-0.01894', '0.0515', '0.01712', '0.0002902', '-0.02823', '-0.00847', '-0.02342', '0.0001131', '-0.0372', '0.04047', '-0.03818', '0.02367', '-0.014305', '-0.0002338', '-0.02672', '-0.03069', '0.0318', '0.00871', '0.01976', '-0.01346', '0.01753', '0.03387', '0.014366', '-0.02354', '0.000876', '0.03357', '-0.04434', '-0.0915', '0.000662', '0.04694', '0.02472', '0.02634', '-0.00813', '-0.018', '0.02333', '0.05612', '0.04416', '-0.05194', '0.0626', '-0.0316', '0.00909', '0.01484', '-0.04752', '0.03583', '0.05026', '0.01243', '0.01645', '-0.00787', '-0.03235', '-0.00584', '0.02028', '-0.010284', '0.01974', '0.003054', '-0.01446', '0.02434', '0.03793', '0.05936', '0.010155', '0.0274', '0.005817', '-0.00726', '0.00506', '0.1039', '0.0093', '0.07135', '-0.0859', '-0.0363', '0.007866']",,,,,,,
mondo:0016639,lower limb deficiency-hypospadias syndrome,"['Fried-Goldberg-Mundel syndrome', 'lower limb malformation-hypospadias syndrome']",,,2487,C2930962,,,,C535640,,,,
mondo:0016641,limb transversal defect-cardiac anomaly syndrome,['Hecht-Scott syndrome'],,,2492,C2931047,,,,C535856,,,,
mondo:0016642,meningioma,"['primary meningeal tumor', 'meningioma (disease)', 'intracranial meningioma', 'meningothelial cell tumour', 'primary meningeal tumour', 'meningothelial cell tumor', 'meningeal neoplasm', 'supratentorial meningioma', 'meningioma']",3565,,2495,C0025286,"['-0.2228', '0.1958', '-0.4148', '0.0744', '-0.2578', '-0.1263', '1.07', '0.553', '-0.39', '-0.1472', '-0.3452', '-0.2489', '0.1131', '0.0711', '0.0602', '0.05206', '0.1254', '-0.261', '0.3352', '-0.2205', '0.09064', '-0.2932', '0.725', '0.2896', '0.1731', '-0.1407', '0.06204', '0.3386', '-0.1534', '0.2223', '0.3994', '-0.1614', '0.6133', '-0.632', '-0.3013', '-0.2917', '-0.5205', '-0.2145', '0.2338', '-0.796', '0.344', '-0.081', '0.3196', '-0.314', '0.949', '0.2192', '-0.2449', '-0.1913', '-0.3862', '0.004234', '0.812', '0.1299', '-0.0712', '0.2234', '0.02652', '0.1006', '-0.517', '-0.01749', '-0.423', '0.541', '-0.3054', '-0.0588', '-0.2854', '0.576', '-0.384', '0.805', '0.3743', '0.976', '0.2097', '0.7793', '0.1536', '0.09436', '-0.05264', '-0.2273', '0.5986', '0.02', '-0.008385', '0.3262', '0.0987', '-0.8926', '-0.04092', '0.07294', '-0.1958', '-0.3904', '-0.374', '-0.0676', '0.3652', '-0.1401', '0.5864', '-0.2034', '-0.02502', '0.4783', '-0.337', '-0.1505', '0.5054', '-0.1512', '-0.223', '-0.06082', '0.1216', '0.1307']",C3230,,D008579,,,10027191,0002858
mondo:0016643,frontonasal dysplasia,"['FND1', 'frontonasal dysplasia 1', 'median cleft syndrome', 'median cleft face syndrome']",0081044,,250,C1876203,,,,C538065,,,,
mondo:0016644,logopenic progressive aphasia,"['Logopenic variant PPA', 'LPA', 'Logopenic primary progressive aphasia']",,,250831,C4049711,,,,,,,,
mondo:0016646,autosomal dominant optic atrophy and peripheral neuropathy,,,,250932,CN201872,,,,,,,,
mondo:0016647,autosomal recessive Stickler syndrome,"['Stickler syndrome, autosomal recessive']",,,250984,CN201875,"['0.6484', '0.05716', '-0.335', '0.2615', '0.3496', '-0.7827', '-0.1561', '0.9214', '-0.924', '-0.9336', '0.1669', '-0.7363', '-0.1683', '0.8296', '0.29', '-0.03256', '-0.4182', '0.4067', '-0.616', '0.06015', '-0.0957', '-0.03085', '0.385', '0.2229', '0.04477', '0.2957', '-0.8105', '0.2222', '0.8564', '0.742', '0.271', '-0.0408', '-0.3904', '0.538', '-0.4346', '0.03436', '-0.2144', '-0.2286', '-0.191', '-0.2041', '0.629', '0.34', '-0.512', '-0.2089', '-0.3914', '-0.4368', '-0.05722', '-0.0667', '0.1578', '-0.0804', '-0.2605', '0.4216', '0.626', '-0.342', '0.197', '-0.4875', '-0.273', '-0.02802', '-0.0958', '-0.2795', '0.982', '0.01131', '-0.3418', '0.004337', '-0.4236', '0.1868', '0.591', '0.4612', '-0.4556', '0.5366', '0.2905', '0.347', '-0.01611', '-0.5317', '0.0616', '0.18', '0.3313', '0.11096', '0.4946', '0.6533', '-0.154', '-0.3044', '0.03168', '0.9014', '-0.771', '0.1587', '0.2465', '0.588', '0.11084', '0.3296', '-0.615', '0.642', '0.14', '0.342', '0.4692', '0.325', '0.656', '-0.1809', '-0.2742', '0.1356']",,,,,,,
mondo:0016648,multiple epiphyseal dysplasia,"['Polyepiphyseal dysplasia', 'multiple epiphyseal dysplasia', 'MED', 'EDM', 'multiple epiphyseal dysplasia (disease)', 'polyepiphyseal dysplasia', 'epiphyseal dysplasia, multiple']",12721,,251,,"['-0.2678', '-0.08044', '0.02397', '-0.1655', '0.5073', '-0.4646', '-0.1852', '0.5166', '-0.633', '-0.3796', '-0.1707', '0.2656', '0.2646', '0.496', '0.01749', '0.2268', '-0.1316', '0.1184', '-0.2808', '-0.4604', '-0.161', '0.404', '0.849', '-0.3264', '0.2793', '0.2302', '0.04105', '-0.4626', '-0.07416', '-0.2744', '-0.2201', '0.2179', '0.0431', '0.6553', '0.2006', '0.011', '-0.3228', '-0.001134', '-0.7046', '-0.0993', '0.491', '-0.4392', '0.252', '0.01671', '0.4202', '-0.4856', '-0.0981', '0.1489', '0.3691', '0.032', '0.415', '0.3325', '0.4736', '0.05283', '0.2054', '-1.123', '-0.0097', '0.1809', '0.06116', '-0.0738', '0.4702', '0.1694', '-0.3394', '0.4048', '0.06494', '-0.1486', '0.1964', '0.4998', '0.339', '0.2615', '-0.159', '-0.04956', '0.219', '-0.1265', '0.573', '0.3176', '0.2357', '0.3816', '0.02039', '-0.0642', '-0.2783', '-0.2345', '-0.3909', '0.909', '-0.2157', '0.2129', '0.1726', '0.1215', '0.1598', '-0.2847', '0.02234', '0.1289', '-0.03537', '-0.05283', '0.4177', '0.4868', '0.595', '-0.1366', '-0.0157', '0.1836']",,,,756.56,Q77.3,10028197,0002654
mondo:0016649,Warburg micro syndrome,"['microcephaly, microcornea, congenital cataract, intellectual disability, optic atrophy and hypogenitalism', 'Warburg micro syndrome', 'micro syndrome', 'WARBM', 'microcephaly, microcornea, congenital cataract, mental retardation, optic atrophy and hypogenitalism', 'Warburg-Sjo-Fledelius syndrome']",0060237,,2510,CN158709,"['-0.406', '0.1514', '-0.2788', '-0.1378', '0.2103', '-0.605', '-0.2103', '0.4866', '-0.6025', '-0.705', '-0.3167', '-0.471', '0.1469', '-0.1539', '-0.04517', '0.2854', '-0.03583', '-0.0982', '-0.1958', '-0.622', '0.2085', '-0.004055', '0.01765', '-0.365', '0.3762', '-0.11633', '-0.06915', '0.3306', '0.4482', '-0.156', '0.481', '0.1622', '0.2935', '0.3757', '0.012665', '0.1115', '-0.0018015', '-0.4631', '0.0744', '-0.02896', '0.626', '0.1875', '0.448', '-0.2316', '0.1357', '-0.662', '-0.3276', '-0.1033', '-0.319', '-0.4106', '-0.0904', '-0.2068', '-0.4326', '0.1333', '-0.0524', '-0.1104', '0.7354', '0.03592', '-0.504', '0.1259', '0.04977', '-0.2328', '0.577', '0.565', '-0.3184', '0.1666', '0.2932', '0.1095', '-0.2778', '0.1301', '-0.5596', '0.2878', '-0.0849', '0.3086', '0.238', '-0.254', '0.3901', '-0.5884', '-0.1371', '0.101', '0.368', '0.4316', '-0.398', '0.935', '-0.03062', '0.243', '0.3247', '0.4502', '-0.04257', '0.601', '0.1316', '0.5015', '-0.1708', '0.1481', '0.685', '-0.1492', '0.4585', '-0.437', '0.7114', '0.11694']",,,,,,,
mondo:0016650,paternal uniparental disomy of chromosome 1,"['UPD(1)pat', 'paternal uniparental disomy of chromosome type 1']",,,251004,,,,,,,,,
mondo:0016651,maternal uniparental disomy of chromosome 1,"['maternal uniparental disomy of chromosome type 1', 'UPD(1)mat']",,,251009,,,,,,,,,
mondo:0016652,2q31.1 microdeletion syndrome,"['Del(2)(q31.1)', 'monosomy 2q31.1']",,,251014,CN201880,,,,,,,,
mondo:0016653,2q33.1 microdeletion syndrome,"['Del(2)(q33.1)', 'monosomy 2q33.1']",,,251028,CN201882,,,,,,,,
mondo:0016654,ring chromosome 5,"['Ring 5', 'chromosome 5 ring', 'Ring chromosome type 5', 'R5', 'rose cluster 5', 'Ring chromosome 5 syndrome']",,,251043,C4050064,,C121984,,,,,,
mondo:0016655,6p22 microdeletion syndrome,"['monosomy 6p22', 'Del(6)(p22)']",,,251046,CN201884,,,,,,,,
mondo:0016656,7q31 microdeletion syndrome,"['Del(7)(q31)', 'monosomy 7q31']",,,251061,CN201886,,,,,,,,
mondo:0016657,8p11.2 deletion syndrome,"['Del(8)(p11.2)', 'monosomy 8p11.2']",,,251066,CN201887,,,,,,,,
mondo:0016658,8p23.1 microdeletion syndrome,"['deletion 8p23.1', '8p23.1 deletion', 'monosomy 8p23.1', 'Del(8)(p23.1)', 'chromosome 8p23.1 deletion']",,,251071,CN201888,,,,C537827,,,,
mondo:0016659,8p23.1 duplication syndrome,"['dup(8)(p23.1p23.1)', 'trisomy 8p23.1']",,,251076,CN201889,,,,,,,,
mondo:0016660,autosomal recessive primary microcephaly,"['microcephalia vera', 'microcephaly vera', 'MCPH', 'microcephaly, primary, autosomal recessive', 'true microcephaly', 'microcephaly, primary autosomal recessive']",0070296,,2512,C3711387,"['0.2852', '0.1489', '0.2573', '-0.2566', '0.1692', '-0.1514', '0.4307', '1.082', '-0.789', '-0.2251', '-0.1748', '0.1991', '0.441', '0.4082', '0.9297', '0.1188', '0.6895', '0.3435', '-0.3457', '-0.7695', '-0.4272', '-0.08325', '0.4348', '0.03305', '0.2108', '0.1997', '-0.2283', '0.0382', '0.0587', '-0.408', '-0.3193', '-0.6616', '0.1829', '0.2646', '-0.5312', '0.7383', '-0.43', '-0.2551', '-0.00832', '-0.11115', '0.3162', '0.0606', '-0.4893', '-0.4336', '0.4749', '-0.582', '0.741', '-0.1816', '0.02556', '-0.0924', '0.3147', '-0.838', '0.011566', '-0.542', '0.1948', '0.4426', '-0.6436', '0.257', '-0.475', '0.1278', '0.3098', '0.2864', '0.4155', '0.06757', '-0.189', '-0.1076', '0.3833', '-0.3247', '-1.125', '0.1746', '-0.6694', '0.783', '0.2406', '-0.566', '0.4263', '0.4363', '0.759', '-0.3882', '-0.6216', '-0.1564', '-0.1458', '0.599', '0.06006', '0.466', '-0.00447', '-0.4126', '0.1881', '-0.2476', '0.742', '0.5786', '0.255', '0.1417', '-0.6016', '-0.003704', '0.09143', '0.3835', '0.7856', '-0.3972', '0.6387', '-1.006']",,,C579935,,,,
mondo:0016661,infantile onset panniculitis with uveitis and systemic granulomatosis,,,,251304,,,,,,,,,
mondo:0016662,idiopathic recurrent pericarditis,['idiopathic relapsing pericarditis'],,,251307,,,,,,,I09.2,,
mondo:0016663,overlapping connective tissue disease,,,,251312,CN201903,,,,,,,10027754,
mondo:0016664,drug-induced vasculitis,"['drug induced vasculitis', 'drug induced cutaneous vasculitis']",,,251325,C3812646,,C112204,,,,,,
mondo:0016666,unexplained long-lasting fever/inflammatory syndrome,,,,251332,CN201905,,,,,,,,
mondo:0016667,sickle cell disease associated with an other hemoglobin anomaly,['Double heterozygotes sickling disorder'],,,251355,CN201907,,,,,,,,
mondo:0016668,sickle cell-beta-thalassemia disease syndrome,"['Hb S beta-thalassemia', 'HbS - beta-thalassemia', 'sickle beta thalassemia', 'HbS-beta-thalassemia syndrome', 'sickle cell-Beta thalassemia', 'sickle cell - beta-thalassemia disease', 'Hb S-Beta thalassemia', 'sickle cell-beta-thalassemia disease syndrome', 'sickle cell-Beta-thalassemia', 'Haemoglobin sickle-beta thalassemia', 'Hemoglobin sickle-beta thalassemia', 'S-Beta thalassemia']",,,251359,,,C95539,,,,,10055579,
mondo:0016669,sickle cell-hemoglobin c disease syndrome,"['HbSC disease', 'sickle cell - haemoglobin C disease', 'sickle cell - hemoglobin C disease']",,,251365,C0019034,,,,,,,10057072,
mondo:0016670,sickle cell-hemoglobin d disease syndrome,"['HbSD disease', 'sickle cell - haemoglobin D disease', 'sickle cell - hemoglobin D disease']",,,251370,C0272084,,,,,,,10056724,
mondo:0016671,sickle cell-hemoglobin E disease syndrome,['HbSE disease'],,,251375,C0272085,,,,,,,,
mondo:0016672,hereditary persistence of fetal hemoglobin-sickle cell disease syndrome,['HPFH-sickle cell disease syndrome'],,613566,251380,CN201912,,,,,,,,
mondo:0016673,"localized junctional epidermolysis bullosa, non-Herlitz type",['JEB-nH loc'],,,251393,CN201914,"['0.6895', '-0.1967', '-0.3408', '0.02805', '0.2153', '-0.572', '-0.648', '0.629', '-0.1514', '-0.8643', '0.3523', '-0.3894', '-1.113', '0.5312', '-0.678', '0.0721', '0.1106', '-1.036', '-0.42', '-1.023', '-0.31', '-0.09686', '0.434', '0.5693', '0.4646', '0.3809', '-1.278', '0.8438', '-0.4187', '-0.7964', '0.2056', '-0.3638', '-0.3489', '0.02821', '0.1676', '0.1216', '-1.196', '0.1337', '1.07', '-0.7534', '0.1527', '-0.6504', '0.02345', '-0.1482', '0.1073', '-0.2864', '-0.1741', '0.1548', '0.5054', '-0.1978', '-0.4468', '-0.7134', '0.5474', '-0.2625', '-0.2238', '-0.5913', '-0.2483', '0.771', '-0.744', '-0.3276', '-0.02486', '0.479', '-0.0489', '0.0269', '0.785', '0.952', '0.254', '0.1366', '-0.846', '0.261', '-0.1792', '0.05753', '-0.5225', '-0.1014', '0.01154', '-0.061', '-0.05463', '0.2551', '0.0792', '-0.0923', '-1.08', '0.277', '-0.362', '-0.2473', '0.2942', '0.413', '-0.984', '0.4937', '0.9443', '0.3914', '-0.6763', '0.348', '-0.03186', '0.6855', '0.08044', '0.628', '0.2937', '-0.581', '0.811', '-0.03214']",,,,,,,
mondo:0016674,"46,XY partial gonadal dysgenesis","['46,XY PGD', '46,XY partial testicular dysgenesis']",,,251510,C4510744,"['0.1287', '0.01313', '-0.1678', '-0.2832', '0.473', '0.05444', '0.2983', '0.3718', '-0.5146', '-1.169', '0.0007424', '-0.383', '0.2546', '0.678', '0.3748', '-0.3074', '0.0949', '-0.1257', '-0.4055', '-0.7124', '-0.1989', '-0.0779', '0.8096', '-0.591', '0.605', '0.1565', '-0.2112', '0.3162', '0.481', '-0.557', '0.821', '-0.03415', '1.117', '-0.312', '-0.2356', '-0.5254', '-0.1628', '-0.2064', '-0.5054', '-0.4888', '0.4448', '-0.03235', '0.06995', '-0.5557', '0.0989', '-0.762', '0.011635', '-1.121', '0.05585', '0.1487', '-0.2384', '-0.2637', '-0.0581', '0.0775', '-0.05414', '0.5815', '0.4646', '-0.02353', '-0.3755', '0.1843', '0.1877', '0.08325', '0.2074', '0.289', '0.3125', '0.6475', '0.3376', '0.2974', '-0.10583', '-0.1759', '0.226', '0.2289', '0.183', '0.1334', '0.573', '-0.8057', '0.1796', '0.5757', '-0.766', '-0.7607', '-0.2224', '0.692', '0.11786', '0.4436', '-0.1737', '-0.5747', '-0.2751', '0.1655', '0.1692', '-0.1277', '-0.4023', '0.659', '-0.364', '-0.5093', '0.3877', '-0.3787', '-0.0147', '-0.4138', '0.07513', '0.3438']",,,,,,,
mondo:0016675,distal arthrogryposis type 10,"['short tendo calcaneus', 'arthrogryposis, distal, type 10', 'DA10', 'tendo calcaneus, short', 'plantar flexion contracture', 'congenital plantar contractures', 'distal arthrogryposis type 10', 'short Achilles tendon']",0111593,187370,251515,C1861238,,,,C566069,,,,
mondo:0016676,recurrent infections-inflammatory syndrome due to zinc metabolism disorder syndrome,['hyperzincemia and hypercalprotectinemia'],,,251523,C1860229,,,,,,,,
mondo:0016677,toxic or drug-related embryofetopathy,,,,251529,,,,,D000014,,,,
mondo:0016678,maternal disease-related embryofetopathy,,,,251535,CN201921,,,,,,,,
mondo:0016680,high grade astrocytic tumor,"['high grade astrocytic neoplasm', 'high-grade astrocytic tumor', 'high-grade astrocytoma', 'high-grade astrocytic tumour', 'high grade astrocytic tumor', 'high-grade astrocytic neoplasm']",,,251561,C3640999,,C102897,,,,,,
mondo:0016681,gliosarcoma,"['glioblastoma with sarcomatous component', 'gliosarcoma', 'sarcomatous glioblastoma', 'glioblastoma with a sarcomatous component']",3071,,251576,C0206726,,C3796,1001465,D018316,,,10018340,
mondo:0016682,giant cell glioblastoma,"['Monstrocellular sarcoma [obs]', 'Monstrocellular sarcoma']",3074,,251579,C0334593,,C4325,,,,,,
mondo:0016683,gliomatosis cerebri,"['gliomatosis', 'astrocytosis cerebri', 'gliomatosis cerebri (morphologic abnormality)', 'gliomatosis cerebri']",6128,,251582,C0334576,,C4318,,,,,10066254,
mondo:0016684,anaplastic astrocytoma,"['grade III astrocytoma', 'grade III astrocytic neoplasm', 'grade III astrocytic tumour', 'malignant astrocytoma', 'astrocytoma, anaplastic, malignant', 'anaplastic astrocytoma', 'grade III astrocytic tumor']",3078,,251589,C0334579,,C9477,0002499,,,,10060971,
mondo:0016685,low-grade astrocytoma,,,,251592,,,,,,,,10065869,
mondo:0016686,diffuse astrocytoma,"['astrocytoma, diffuse', 'protoplasmic astrocytoma (histologic variant)', 'grade II astrocytoma', 'gemistocytic astrocytoma (histologic variant)', 'fibrillary astrocytoma (histologic variant)', 'grade II astrocytic tumor', 'astrocytoma, diffuse, malignant', 'diffuse astrocytoma', 'WHO grade II astrocytoma', 'low-grade diffuse astrocytoma', 'grade II astrocytic neoplasm', 'grade II astrocytic tumour']",4857,,251595,C0280785,,C7173,,,,,,
mondo:0016687,protoplasmic astrocytoma,"['protoplasmic astrocytoma', 'protoplasmic astrocytic tumour', 'protoplasmic astrocytoma (morphologic abnormality)', 'protoplasmic astrocytic tumor']",7008,,251598,C0334580,,C4320,,,,,,
mondo:0016688,fibrillary astrocytoma,"['fibrillary astrocytoma', 'fibrillary astrocytic tumors', 'fibrillary astrocytic tumours']",6726,,251601,C0334582,,C4322,,,,,10065889,
mondo:0016689,gemistocytic astrocytoma,"['gemistocytic astrocytic tumour', 'gemistocytic astrocytoma (morphologic abnormality)', 'gemistocytic astrocytic tumor', 'Gemistocytoma', 'gemistocytic astrocytoma']",7005,,251604,C0334581,,C4321,,,,,,
mondo:0016690,pleomorphic xanthoastrocytoma,"['pleomorphic Xantho-astrocytoma', 'PXA']",4852,,251607,C0334586,,C4323,,,,,,
mondo:0016691,pilocytic astrocytoma,"['grade I astrocytic neoplasm', 'grade I astrocytic tumour', 'astrocytoma, benign', 'grade I astrocytic tumor', 'Piloid astrocytoma', 'pilocytic astrocytoma', 'astrocytoma, pilocytic, benign', 'grade I astrocytoma']",4851,,251612,C0334583,,C4047,,,,,,
mondo:0016692,pilomyxoid astrocytoma,['PMA'],4845,,251615,C1519086,,C40315,,,,,,
mondo:0016693,subependymal giant cell astrocytoma,"['subependymal giant cell astrocytic tumour', 'subependymal giant cell astrocytic tumor', 'subependymal giant cell astrocytoma (morphologic abnormality)', 'SEGA', 'subependymal giant cell astrocytic neoplasm']",5077,,251618,C0205768,,C3696,,,,,,
mondo:0016695,oligodendroglioma,"['WHO grade II oligodendroglial neoplasm', 'well differentiated oligodendroglial tumour', 'well differentiated oligodendroglial tumor', 'oligodendroglial tumour', 'oligodendroglial neoplasm', 'oligodendroglial tumor', 'WHO grade II oligodendroglial tumour', 'well differentiated oligodendroglioma', 'WHO grade II oligodendroglial tumor', 'oligodendroglioma']",3181,,251627,,,C3288,,D009837,,,10030286,
mondo:0016696,anaplastic oligodendroglioma,"['oligodendroglioma, malignant', 'WHO grade III oligodendroglial tumor', 'undifferentiated oligodendroglioma', 'WHO grade III oligodendroglial neoplasm', 'WHO grade III oligodendroglial tumour', 'anaplastic oligodendroglioma', 'malignant oligodendroglioma', 'oligodendroglioma, anaplastic, malignant']",7154,,251630,C0334590,,C4326,0002501,,,,10026659,
mondo:0016697,low grade ependymoma,,,,251633,CN201940,,,,,,,,
mondo:0016698,ependymoma,"['WHO grade II ependymal tumor', 'tanycytic ependymoma (histologic variant)', 'ependymoma, benign', 'ependymoma, familial', 'epithelial ependymoma', 'papillary ependymoma (histologic variant)', 'WHO grade II ependymal tumour', 'WHO grade II ependymal neoplasm', 'clear cell ependymoma (histologic variant)', 'benign ependymoma', 'ependymoma']",4844,,251636,CN201941,,C3017,,D004806,,,10014967,
mondo:0016699,myxopapillary ependymoma,"['myxopapillary ependymoma (morphologic abnormality)', 'myxopapillary ependymoma', 'ependymoma, benign']",5075,,251643,C0205769,,C3697,,D004806,,,,
mondo:0016700,anaplastic ependymoma,"['undifferentiated ependymal tumor', 'WHO grade III ependymal tumour', 'WHO grade III ependymal neoplasm', 'malignant ependymoma', 'undifferentiated ependymoma', 'WHO grade III ependymal tumor', 'ependymoma, malignant', 'anaplastic ependymal neoplasm', 'undifferentiated ependymal tumour', 'anaplastic ependymal tumour', 'ependymal tumours', 'ependymal tumors', 'high-grade ependymoma', 'anaplastic ependymoma', 'ependymoma, anaplastic, malignant', 'undifferentiated ependymal neoplasm', 'anaplastic ependymal tumor']",5889,,251646,C1333407,,C6770,,,,,10014968,
mondo:0016701,oligoastrocytic tumor,"['mixed oligodendroglial and astrocytic tumour', 'mixed oligodendroglial and astrocytic tumor']",,,251651,CN201945,,,,,,,,
mondo:0016702,oligoastrocytoma,"['mixed oligo-astrocytoma', 'glioma, mixed, benign', 'mixed astrocytoma-oligodendroglioma', 'oligoastrocytoma', 'MOA', 'mixed astrocytic-oligodendroglial tumor', 'mixed oligodendroglioma-astrocytoma', 'WHO grade II mixed glioma', 'mixed astrocytic-oligodendroglial neoplasm', 'mixed astrocytic-oligodendroglial tumour', 'mixed oligoastrocytoma']",7912,,251656,C0280793,,C4050,0000630,D009837,,,10027744,
mondo:0016703,anaplastic oligoastrocytoma,"['anaplastic oligoastrocytoma', 'aMOA', 'WHO grade III mixed glioma', 'anaplastic mixed glioma', 'AOAST']",,,251663,C0431108,,C6959,0002500,,,,,
mondo:0016705,angiocentric glioma,"['angiocentric neuroepithelial tumour', 'ANGL', 'Monomorphus angiocentric glioma', 'angiocentric neuroepithelial tumor', 'angiocentric glioma (WHO grade I)']",0081261,,251671,C2363903,,C92552,,,,,,
mondo:0016706,chordoid glioma of the third ventricle,"['chordoid glioma of the 3rd ventricle', 'chordoid glioma of 3rd ventricle', 'third ventricle chordoid glioma', 'chordoid glioma of the third ventricle (WHO grade II)', 'chordoid glioma of third ventricle', 'chordoid glioma', 'chordoid glioma (morphologic abnormality)', 'chordoid glioma of the third ventricle']",3774,,251674,C1322252,,C5592,,,,,,
mondo:0016707,astroblastoma,"['astroblastoma (morphologic abnormality)', 'astroblastoma', 'AstB', 'cerebral astroblastoma']",7305,,251679,C0334587,,C4324,,,,,,
mondo:0016708,embryonal tumor of neuroepithelial tissue,,,,251852,CN201955,,,,,,,,
mondo:0016709,anaplastic/large cell medulloblastoma,['large cell/anaplastic medulloblastoma'],,,251855,C4330531,,C129436,,,,,,
mondo:0016710,medulloblastoma with extensive nodularity,"['nodular medulloblastoma', 'MBEN', 'medulloblastoma with extensive nodularity and advanced neuronal differentiation', 'cerebellar neuroblastoma', 'medulloblastoma with extensive nodularity']",,,251858,CN201957,,C5407,,,,,,
mondo:0016711,desmoplastic/nodular medulloblastoma,"['desmoplastic medulloblastoma', 'desmoplastic/nodular medulloblastoma', 'desmoplastic nodular medulloblastoma', 'Desmoplastic medulloblastoma']",,,251863,C0751291,,C4956,0005699,,,,,
mondo:0016712,classic medulloblastoma,['classic medulloblastoma'],,,251867,C1707400,,C54039,,,,,,
mondo:0016713,central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor,"['central nervous system PNET', 'central nervous system Ewing sarcoma/peripheral primitive neuroectodermal tumor', 'central nervous system primitive neuroectodermal tumour', 'central nervous system primitive neuroectodermal tumor', 'CNS PNET']",,,251870,,,C129537,,,,,10057846,
mondo:0016715,ependymoblastoma,"['embryonal tumor with Multilayered Rosettes, C19MC-altered', 'embryonal tumor with abundant neuropil and true Rosettes', 'embryonal tumour with abundant neuropil and true Rosettes', 'ETANTR', 'embryonal tumour with abundant neuropil and true rosettes', 'embryonal tumor with Multilayered Rosettes', 'neuroectodermal tumours primitive', 'ependymoblastoma', 'embryonal tumor with abundant neuropil and true rosettes', 'ETMR, C19MC-altered', 'embryonal tumour with Multilayered Rosettes with C19MC amplification', 'embryonal tumour with Multilayered Rosettes', 'neuroectodermal tumors primitive', 'embryonal tumor with Multilayered Rosettes with C19MC amplification', 'embryonal tumour with Multilayered Rosettes, C19MC-altered', 'ETMR']",4794,,251880,C0700367,,C4915,,,,,10014966,
mondo:0016717,choroid plexus neoplasm,"['tumor of choroid plexus', 'choroid plexus neoplasm', 'choroid plexus tumour', 'neoplasm of choroid plexus', 'choroid plexus tumor', 'tumor of the choroid plexus', 'tumour of choroid plexus', 'tumour of the choroid plexus', 'neoplasm of the choroid plexus']",,,251896,C0085138,,C3473,,,,,,
mondo:0016718,choroid plexus carcinoma,"['choroid plexus carcinoma (morphologic abnormality)', 'carcinoma, choroid plexus, malignant', 'malignant neoplasm of the choroid plexus', 'malignant tumour of choroid plexus', 'choroid plexus cancer', 'malignant tumor of choroid plexus', 'cancer of choroid plexus', 'carcinoma of the choroid plexus', 'choroid plexus carcinoma', 'cancer of the choroid plexus', 'anaplastic choroid plexus papilloma', 'malignant neoplasm of choroid plexus', 'carcinoma of choroid plexus']",5648,,251899,,,C4715,,C562943,,,10067478,
mondo:0016719,microcephaly-seizures-intellectual disability-heart disease syndrome,"['microcephaly, seizures, intellectual disability, congenital heart disease, and skeletal abnormalities', 'microcephaly seizures mental retardation heart disorders', 'microcephaly, seizures, mental retardation, congenital heart disease, and skeletal abnormalities', 'microcephaly seizures intellectual disability heart disorders']",,,2519,C2931529,,,,C537544,,,,
mondo:0016721,pineal tumor of neuroepithelial tissue,,,,251905,CN201969,,,,,,,,
mondo:0016722,pineoblastoma,"['pineal gland PNET', 'pineoblastoma, malignant', 'pineal gland primitive neuroectodermal tumor', 'PNET of the pineal gland', 'primitive neuroectodermal tumor of the pineal gland', 'pineal gland primitive neuroectodermal tumour', 'pineal PNET', 'primitive neuroectodermal tumour of pineal gland', 'primitive neuroectodermal tumor of pineal gland', 'primitive neuroectodermal neoplasm of the pineal gland', 'pineal primitive neuroectodermal tumour', 'primitive neuroectodermal tumour of the pineal gland', 'pineal primitive neuroectodermal tumor', 'pineoblastoma', 'pineal primitive neuroectodermal neoplasm', 'pineal gland primitive neuroectodermal neoplasm', 'pineoblastoma (WHO grade IV)', 'primitive neuroectodermal neoplasm of pineal gland', 'PNET of pineal gland']",1664,,251909,C0205898,,C9344,1000475,,,,10050487,
mondo:0016723,pineocytoma,"['pineocytoma, benign', 'benign pinealoma', 'Pineocytoma (WHO grade I)', 'pinealocytoma', 'pineocytoma', 'pineocytoma (disease)']",0081248,,251912,C0917890,,C6966,1000476,,,,10035059,0030407
mondo:0016724,papillary tumor of the pineal region,['PTPR'],0081251,,251915,C2985219,,C92624,1000451,,,,,
mondo:0016725,pineal parenchymal tumor of intermediate differenciation,,,,251919,CN201973,,,,,,,,
mondo:0016726,neuronal tumor,,,,251924,CN201974,,,,,,,,
mondo:0016727,extraventricular neurocytoma,"['EVN', 'extraventricular neurocytoma (WHO grade II)']",0081314,,251927,CN201975,,C92555,,,,,,
mondo:0016729,mixed neuronal-glial tumor,"['neuronal and Glio-neuronal tumor', 'neuronal and mixed neuronal-glial tumor', 'neuronal and Glio-neuronal tumour', 'neuronal and mixed neuronal-glial tumour', 'neuronal and Glio-neuronal neoplasm', 'neuronal and mixed neuronal-glial tumors', 'neuronal and mixed neuronal-glial tumours']",,,251934,CN201977,,C4747,,,,,,
mondo:0016730,gangliocytoma,['GNC'],2426,,251937,CN201978,,C6934,,D005729,,,,
mondo:0016731,desmoplastic infantile astrocytoma/ganglioglioma,['DIA/DIG'],,,251940,CN201979,,,,,,,,
mondo:0016733,ganglioglioma,"['mixed cell tumors containing both neural ganglionic cells and neural glial cell components', 'adult ganglioglioma', 'CNS ganglioglioma', 'mixed cell tumours containing both neural ganglionic cells and neural glial cell components', 'ganglioglioma', 'childhood ganglioglioma']",5078,,251949,C0206716,,C3788,0003094,D018303,,,10017701,
mondo:0016734,anaplastic ganglioglioma,['AGNG'],,,251957,C0431112,,C4717,,,,,,
mondo:0016735,papillary glioneuronal tumor,"['papillary glioneuronal tumor (WHO grade I)', 'PGNT', 'pseudopapillary ganglioglioneurocytoma', 'papillary glioneuronal tumour (WHO grade I)', 'pseudopapillary neurocytoma with glial differentiation']",0081283,,251962,C2985174,,C92554,,,,,,
mondo:0016736,rosette-forming glioneuronal tumor of fourth ventricule,"['rosette-forming glioneuronal tumor', 'rosette-forming glioneuronal tumour', 'dysembryoplastic neuroepithelial tumour of cerebellum', 'dysembryoplastic neuroepithelial tumor of cerebellum', 'DNT of the cerebellum', 'RGNT']",0081284,,251975,CN201984,,C129431,,,,,,
mondo:0016738,primary germ cell tumor of central nervous system,"['primary germ cell tumour of CNS', 'primary germ cell tumor of CNS']",,,251995,CN201986,,,,,,,,
mondo:0016739,yolk sac tumor of central nervous system,"['central nervous system yolk Sac tumor', 'intracranial endodermal sinus tumor', 'central nervous system yolk Sac tumour', 'yolk sac tumour of CNS', 'CNS yolk Sac tumour', 'endodermal sinus tumour of central nervous system', 'CNS yolk Sac tumor', 'yolk Sac tumour of the central nervous system', 'yolk Sac tumor of the CNS', 'intracranial endodermal sinus tumour', 'yolk Sac tumor of central nervous system', 'intracranial yolk sac tumor', 'endodermal sinus tumor of CNS', 'yolk Sac tumour of CNS', 'endodermal sinus tumor of central nervous system', 'yolk Sac tumour of the CNS', 'endodermal sinus tumour of CNS', 'intracranial yolk sac tumour', 'yolk sac tumor of CNS', 'yolk Sac tumour of central nervous system', 'yolk Sac tumor of the central nervous system', 'yolk Sac tumor of CNS']",,,252006,CN201987,,C7011,,,,,,
mondo:0016740,choriocarcinoma of the central nervous system,"['choriocarcinoma of the CNS', 'choriocarcinoma of CNS', 'central nervous system choriocarcinoma (disease)', 'central nervous system choriocarcinoma']",,,252015,CN201988,,C7012,,,,,,
mondo:0016742,mixed germ cell tumor of central nervous system,"['mixed germ cell tumor of the central nervous system', 'mixed germ cell tumour of CNS', 'mixed germ cell tumour of the CNS', 'mixed germ cell tumour of the central nervous system', 'mixed germ cell tumor of the CNS', 'central nervous system mixed germ cell tumor', 'mixed germ cell neoplasm of the central nervous system', 'central nervous system mixed germ cell tumour', 'CNS mixed germ cell tumor', 'mixed germ cell tumor of CNS', 'CNS mixed germ cell tumour']",,,252021,CN201989,,C7016,,,,,,
mondo:0016743,tumor of meninges,"['meningeal cluster rare nervous system tumour', 'tumor of the meninges', 'meningeal tumour', 'meningeal cluster tumour', 'meningeal neoplasms', 'meningothelial tumour', 'tumour of meningeal cluster', 'meninges tumour', 'tumor of meningeal cluster', 'tumor of meninges', 'meningeal cluster neoplasm (disease)', 'meningeal tumor', 'meninges neoplasm', 'neoplasm of the meninges', 'meningeal cluster rare nervous system tumor', 'meninges tumor', 'tumour of the meninges', 'meningothelial tumor', 'neoplasm of meningeal cluster', 'meningeal cluster tumor', 'neoplasm of meninges', 'meningeal neoplasm']",,,252025,C0025284,,C3229,,,239.7,,10061282,
mondo:0016744,primary melanocytic tumor of central nervous system,"['primary melanocytic lesion of CNS', 'primary melanocytic tumor of CNS', 'primary melanocytic tumour of CNS', 'primary melanocytic lesion of central nervous system']",,,252028,CN201991,,,,,,,,
mondo:0016745,diffuse leptomeningeal melanocytosis,"['leptomeningeal melanomatosis', 'DLM']",,,252031,,,,,,,,,
mondo:0016746,meningeal melanocytoma,"['melanocytoma of the meninges', 'melanocytoma of meninges', 'meninges melanocytoma', 'leptomeningeal melanocytoma']",5900,,252046,C1266113,,C4662,1000370,,,,,
mondo:0016747,primary melanoma of the central nervous system,"['CNS melanoma', 'malignant melanoma of meninges', 'melanoma of the Central nervous system', 'melanoma of central nervous system', 'primary CNS melanoma', 'primary melanoma of the CNS', 'melanoma of CNS', 'primary meningeal melanoma', 'melanoma of the CNS', 'Central nervous system melanoma', 'central nervous system melanoma (disease)']",,,252050,CN201994,,C5505,,,,,,
mondo:0016748,hemangioblastoma,"['capillary hemangioblastoma', 'angioblastoma', 'hemangioblastoma', 'HMBL']",5241,,252054,C0206734,,C3801,,D018325,,D33.4,10018813,
mondo:0016749,tumor of cranial and spinal nerves,"['rare tumor of cranial and spinal nerves', 'rare tumour of cranial and spinal nerves']",,,252057,CN201996,,,,,,,,
mondo:0016750,microcephaly-cleft palate syndrome,"['microcephaly-cleft palate-abnormal retinal pigmentation syndrome', 'Halal syndrome', 'microcephaly cleft palate autosomal dominant']",,,2521,C2930954,,,,C535622,,,,
mondo:0016751,malignant perineurioma,"['perineurial malignant peripheral nerve sheath tumor', 'perineurial malignant peripheral nerve sheath tumour', 'malignant peripheral nerve sheath tumour with perineurial differentiation', 'malignant peripheral nerve sheath tumor with perineurial differentiation', 'perineurioma, malignant']",,,252128,C1266188,,C66845,,,,,,
mondo:0016752,benign peripheral nerve sheath tumor,['BPNST'],,,252131,CN202000,,,,,,,,
mondo:0016755,neurofibroma,"['neurofibroma (WHO grade I)', 'NFIB', 'neurofibroma, benign', 'neurofibroma']",962,,252183,C0027830,,C3272,0000622,D009455,215.9,,10029267,
mondo:0016756,inherited nervous system cancer-predisposing syndrome,,,,252190,CN202004,,,,,,,,
mondo:0016757,malignant triton tumor,"['malignant peripheral nerve sheath tumour with rhabdomyosarcoma', 'malignant peripheral nerve sheath tumour with rhabdomyosarcomatous differenciation', 'malignant tumour of peripheral nerve sheath with rhabdomyosarcoma', 'malignant peripheral nerve sheath neoplasm with rhabdomyosarcoma', 'malignant tumor of the peripheral nerve sheath with rhabdomyosarcoma', 'malignant peripheral nerve sheath tumor with rhabdomyosarcoma', 'malignant peripheral nerve sheath tumor with rhabdomyosarcomatous differenciation', 'malignant tumor of peripheral nerve sheath with rhabdomyosarcoma', 'MPNST with rhabdomyoblastic differentiation', 'malignant neoplasm of peripheral nerve sheath with rhabdomyosarcoma', 'malignant Triton tumour', 'MPNST with rhabdomyosarcomatous differentiation', 'malignant Triton tumor', 'malignant tumour of the peripheral nerve sheath with rhabdomyosarcoma', 'MTT', 'malignant neoplasm of the peripheral nerve sheath with rhabdomyosarcoma', 'MPNST with rhabdomyosarcoma']",6707,,252212,C0334616,,C4335,,,171.9,,,
mondo:0016758,microcephaly-brain defect-spasticity-hypernatremia syndrome,"['Franek-Bocker-Kahlen syndrome', 'microcephaly - brain defect - spasticity - hypernatremia', 'microcephaly brain defect spasticity hypernatremia']",,,2523,CN202009,"['0.1114', '-0.01802', '0.5605', '-0.04416', '-0.03857', '-0.2047', '-0.03732', '0.4722', '-1.07', '-0.429', '-0.1898', '-0.2578', '0.31', '0.337', '0.917', '-0.2026', '0.3713', '-0.09796', '-0.5156', '-0.9043', '-0.1072', '-0.00821', '0.2822', '-0.187', '0.2246', '0.141', '-0.2979', '0.2668', '0.1396', '-0.4294', '-0.2495', '-0.2886', '0.4675', '-0.5596', '-0.0973', '0.959', '-0.6035', '-0.3445', '0.05124', '-0.1952', '0.07446', '0.10913', '-0.654', '-0.802', '0.311', '-0.1671', '0.8687', '-0.1566', '-0.506', '-0.381', '0.03818', '-0.7817', '0.02382', '-0.1995', '-0.04498', '0.4465', '-0.693', '0.2062', '-0.552', '0.1354', '0.5366', '0.3386', '0.1989', '0.4297', '-0.12317', '-0.4214', '0.2147', '-0.00647', '-1.337', '0.02353', '-0.6245', '1.32', '-0.07983', '-0.6523', '0.04108', '0.2026', '0.5537', '-0.2269', '-0.3538', '0.2201', '-0.3787', '0.6475', '0.07434', '0.9175', '0.3928', '-0.5737', '0.2986', '-0.2632', '0.759', '0.4255', '0.11664', '-0.01848', '0.04535', '0.3228', '0.2478', '0.3574', '1.128', '-1.032', '1.039', '-0.7407']",,,,,,,
mondo:0016759,pontocerebellar hypoplasia type 2,"['PCH2', 'progressive microcephaly from birth extrapyramidal dyskinesia chorea epilepsy']",0112328,,2524,C2932714,"['0.0958', '0.517', '0.11945', '-0.334', '-0.167', '-0.731', '-0.02515', '0.452', '-0.8237', '-0.325', '-0.2136', '-0.5024', '-0.3623', '-0.08606', '0.8267', '-0.0745', '0.454', '-0.676', '-0.013275', '-0.8657', '-0.1718', '-0.1704', '0.5454', '-0.0752', '0.3008', '0.1664', '0.3171', '0.012184', '-0.1332', '-0.1018', '0.03516', '0.4548', '0.3396', '0.2052', '-0.26', '0.4695', '-0.04022', '-0.0008383', '0.05267', '0.0994', '0.2294', '-0.1455', '-0.2114', '0.6743', '-0.06866', '-0.3303', '0.08813', '-0.01248', '0.03214', '0.403', '-0.09125', '-0.258', '0.0107', '-0.3904', '0.01273', '-0.05643', '0.267', '-0.1807', '-0.01753', '0.3757', '0.02103', '0.6484', '1.074', '0.276', '-0.799', '-0.04196', '-0.003845', '0.1879', '-0.506', '0.83', '0.2583', '0.402', '-0.1583', '0.0186', '0.1567', '0.1711', '0.02469', '-0.355', '-1.258', '-0.1564', '0.07086', '0.2338', '0.4155', '0.579', '-0.1818', '0.1555', '-0.1384', '0.303', '1.08', '-0.06555', '-0.02466', '0.8115', '0.01114', '0.4255', '-0.0972', '0.164', '0.4001', '0.265', '0.6772', '0.1833']",C124057,,C548070,,,,
mondo:0016760,"microcephaly-microcornea syndrome, Seemanova type","['Seemanova-Lesny syndrome', 'Seemanova Lesny syndrome', 'X-linked microcephaly, microphthalmia, microcornea, congenital cataract, hypogenitalism, mental deficiency, growth retardation', 'microcephaly microcornea syndrome Seemanova type']",,,2528,,,,,C537539,,,,
mondo:0016761,spondyloepiphyseal dysplasia,"['spondyloepiphyseal dysplasia and spondyloepimetaphyseal dysplasia', 'SED and SEMD']",0112280,,253,,"['-0.3577', '0.2491', '0.203', '-0.1735', '0.2878', '-0.185', '-0.01636', '0.319', '-0.2345', '-0.1207', '-0.0763', '0.0662', '-0.0197', '-0.00756', '-0.01404', '0.0115', '0.075', '-0.10315', '-0.1481', '-0.3875', '0.01863', '-0.036', '0.3127', '-0.1602', '0.072', '0.006756', '-0.03885', '-0.07196', '0.04218', '-0.00129', '0.002419', '-0.1528', '0.04565', '-0.01153', '0.1405', '-0.0579', '0.1293', '-0.1324', '0.0544', '-0.2112', '0.06836', '-0.1192', '-0.08417', '-0.07404', '-0.05362', '-0.165', '0.0401', '0.1637', '0.1737', '-0.242', '0.1161', '-0.1368', '0.02145', '0.135', '-0.2546', '-0.2695', '0.1161', '-0.1128', '-0.2196', '0.07635', '0.2476', '0.0368', '-0.3071', '0.02248', '-0.11707', '-0.0685', '0.201', '0.1637', '-0.1403', '0.1779', '-0.1393', '0.04257', '0.11993', '-0.1677', '-0.105', '-0.004242', '-0.0842', '0.2021', '-0.0921', '-0.2678', '-0.0962', '0.0166', '0.02176', '0.1838', '-0.2122', '0.0332', '0.168', '0.2081', '0.1721', '0.06824', '-0.2483', '0.2427', '-0.0236', '0.05072', '0.4177', '0.0339', '0.2546', '-0.356', '0.1328', '0.1371']",,,,756.9,,10062920,
mondo:0016762,microcornea-corectopia-macular hypoplasia syndrome,['microcornea corectopia macular hypoplasia'],,,2535,C2931531,,,,C537551,,,,
mondo:0016763,spondylometaphyseal dysplasia,,0112295,,254,,,,,,,,,
mondo:0016764,isolated anophthalmia-microphthalmia syndrome,"['MAC spectrum', 'isolated pure microphthalmia', 'primitive anophthalmia', 'clinical anophthalmia', 'isolated anophthalmia - microphthalmia', 'nonsyndromic anophthalmia-microphthalmia syndrome', 'microphthalmia-anophthalmia-coloboma spectrum']",,,2542,CN202019,,,,,,,,
mondo:0016765,19p13.12 microdeletion syndrome,"['monosomy 19p13.12', 'Chromosome19p13.12 microdeletion', 'Del(19)(p13.12)']",,,254346,CN202023,,,,,,,,
mondo:0016769,linear lichen planus,"['llp', 'Blaschkoid lichen planus', 'linear LP', 'Blaschkoid LP']",,,254379,C0023650,,,,,,,,
mondo:0016770,actinic lichen planus,"['lichen planus actinus', 'summertime actinic lichenoid eruption', 'lichen planus subtropicus', 'lichen planus tropicus', 'lichenoid melanodermatitis', 'actinic LP']",,,254395,C0406365,,,,,,,,
mondo:0016771,annular atrophic lichen planus,['annular atrophic LP'],,,254411,C4304037,,,,,,,,
mondo:0016772,annular lichen planus,['annular LP'],,,254424,C0406363,,,,,,,,
mondo:0016773,atrophic lichen planus,['atrophic LP'],,,254449,C0023647,,C34777,,,,,10056959,
mondo:0016774,lichen planus pigmentosus,"['LP pigmentosus', 'lichen planus pigmentosus inversus', 'lichen planus pigmentosa', 'LP pigmentosa']",,,254463,C0406366,,,,,,,,
mondo:0016775,lichen planus pemphigoides,['LP pemphigoides'],,,254478,C0406369,,,,,,,,
mondo:0016776,frontal fibrosing alopecia,['FFA'],,,254492,C4255374,,,,,,L66.1,,
mondo:0016777,inhalational botulism,['inhalation botulism'],,,254504,C1443900,,,,,,,,
mondo:0016778,iatrogenic botulism,"['inadvertent botulism', 'accidental botulism']",,,254509,C4288922,,C128345,,,,,,
mondo:0016779,multiple congenital anomalies due to 14q32.2 maternally expressed gene defect,"['MCA due to 14q32.2 maternally expressed gene defect', 'Kagami-Ogata syndrome']",0111712,,254519,,,,,,,,,
mondo:0016780,paternal 14q32.2 microdeletion syndrome,"['paternal del(14)(q32.2)', 'paternal monosomy 14q32.2']",,,254525,CN202036,,,,,,,,
mondo:0016781,maternal 14q32.2 microdeletion syndrome,"['maternal monosomy 14q32.2', 'maternal del(14)(q32.2)']",,,254528,CN202037,,,,,,,,
mondo:0016782,paternal 14q32.2 hypomethylation syndrome,,,,254531,CN202038,,,,,,,,
mondo:0016783,maternal 14q32.2 hypermethylation syndrome,,,,254534,CN202039,,,,,,,,
mondo:0016785,complete hydatidiform mole,"['complete hydatid Mole', 'classical hydatidiform Mole', 'complete molar pregnancy', 'complete Mole']",,,254688,C0678213,,C4871,,,,,,
mondo:0016786,partial hydatidiform mole,"['partial hydatid Mole', 'incomplete hydatid Mole', 'incomplete hydatidiform mole', 'incomplete molar pregnancy', 'partial Mole', 'partial molar pregnancy', 'PHM']",,,254693,C0334529,,C4293,,,,,,
mondo:0016787,epithelioid trophoblastic tumor,"['ETT', 'epithelioid trophoblastic tumor']",3593,,254698,C1266159,,C6900,,,,,,
mondo:0016789,pyruvate metabolism disorder,"['rare inborn error of pyruvate metabolic process', 'inborn error of pyruvate metabolic process']",,,254746,CN226999,,,,,,,,
mondo:0016790,tricarboxylic acid cycle disorder,"['Krebs cycle disorder', 'inborn error of tricarboxylic acid cycle', 'citric acid cycle disorder', 'rare inborn error of tricarboxylic acid cycle', 'TCA cycle disorder']",,,254749,CN227000,,,,,,,,
mondo:0016794,maternally-inherited mitochondrial myopathy,,,,254788,,,,,,,,,
mondo:0016796,"mitochondrial DNA depletion syndrome, encephalomyopathic form","['mtDNA depletion syndrome, encephalomyopathic form']",,,254803,CN230130,"['-0.3784', '0.3171', '0.2253', '0.06433', '0.1829', '-0.2411', '0.2231', '0.3315', '-0.3289', '0.04544', '-0.2361', '-0.2289', '0.04117', '-0.0522', '-0.07947', '-0.0003455', '-0.00441', '-0.1024', '-0.1425', '-0.545', '0.2307', '-0.1564', '0.366', '-0.03004', '0.2085', '0.01491', '-0.2751', '-0.05368', '-0.0753', '-0.067', '0.1531', '0.291', '0.4224', '0.1903', '0.03564', '-0.2177', '-0.441', '-0.02339', '-0.4302', '-0.1335', '0.00885', '-0.439', '-0.01041', '0.1985', '-0.0485', '-0.367', '-0.2358', '0.01382', '0.1451', '0.1215', '-0.269', '0.2329', '0.02475', '-0.1555', '0.2294', '-0.533', '0.1365', '-0.1067', '-0.2104', '0.1986', '0.3162', '-0.07886', '0.2316', '-0.03616', '-0.2051', '-0.1755', '0.1786', '0.3252', '-0.2185', '0.3726', '-0.302', '0.092', '0.2461', '0.2087', '0.01368', '0.1024', '0.2566', '0.06335', '-0.2593', '-0.0136', '0.2654', '0.1084', '-0.09143', '0.3784', '0.02641', '0.1515', '0.2059', '0.2494', '0.311', '0.1808', '0.592', '0.2656', '-0.06506', '0.02641', '0.1398', '0.3784', '0.4578', '-0.1472', '0.08356', '0.2316']",,,,,,,
mondo:0016797,multiple mitochondrial DNA deletion syndrome,['multiple mtDNA deletion syndrome'],,,254807,CN202053,,,,,,,,
mondo:0016798,ataxia neuropathy spectrum,,,,254818,C3683791,,,,C579922,,,,
mondo:0016800,mitochondrial membrane transport disorder,,,,254827,CN227001,,,,,,,,
mondo:0016801,mitochondrial substrate carrier disorder,,,,254830,CN227002,,,,,,,,
mondo:0016802,mitochondrial protein import disorder,,,,254834,CN227003,,,,,,,,
mondo:0016803,unspecified inborn mitochondrial disorder,['unspecified mitochondrial disorder'],,,254837,CN227004,,,,,,,,
mondo:0016805,isolated oxidative phosphorylation complex disorder,['isolated respiratory chain complex disorder'],,,254846,CN227005,,,,,,,,
mondo:0016806,maternally-inherited mitochondrial dystonia,,,,254851,C4274074,,,,,,,,
mondo:0016807,pure mitochondrial myopathy,,,,254854,C4517289,,,,,,,,
mondo:0016809,spinocerebellar ataxia with epilepsy,"['SCAE', 'MSCAE', 'mitochondrial spinocerebellar ataxia with epilepsy']",,,254881,CN202060,"['0.953', '0.0911', '-0.3833', '0.12085', '-0.5273', '-0.4038', '0.676', '0.2482', '-0.5415', '-0.317', '0.0164', '-0.2192', '-0.4998', '0.4578', '0.02779', '-0.1469', '-0.1456', '-0.4084', '-0.4065', '-0.503', '-0.4104', '0.4712', '0.0521', '-0.4365', '-0.2778', '-0.03976', '-0.0158', '-0.0944', '-0.493', '0.5005', '0.1588', '-0.681', '0.203', '0.0789', '0.8813', '0.3574', '-0.06726', '0.1859', '-0.2798', '-0.4126', '-0.2979', '-0.418', '0.1084', '-0.1255', '-0.628', '-0.9434', '-0.1943', '0.2795', '0.563', '0.5596', '-0.2285', '0.1598', '0.0656', '-0.4993', '-0.08496', '-0.2725', '-0.01833', '0.0376', '-0.266', '0.1361', '-0.8374', '0.498', '0.8496', '-0.293', '-0.4956', '1.329', '0.03226', '-0.0984', '-0.9814', '0.807', '1.11', '1.046', '-0.01115', '-0.3325', '0.0623', '0.569', '0.8022', '0.4756', '-0.1708', '0.3423', '-0.05997', '0.802', '0.317', '0.3674', '0.3003', '0.2208', '0.1271', '0.7095', '0.742', '0.4402', '0.1131', '-0.02715', '-0.0508', '0.0704', '0.1125', '0.3328', '0.2961', '-0.4275', '0.1278', '0.3274']",,,C564395,,,,
mondo:0016810,autosomal recessive progressive external ophthalmoplegia,"['arPEO', 'progressive external ophthalmoplegia, autosomal recessive']",,,254886,,"['-0.6035', '0.2306', '-0.1968', '-0.10223', '-0.1015', '-0.6587', '0.2654', '0.3079', '-0.6685', '-0.0873', '-0.1771', '0.002007', '-0.3394', '0.2269', '0.2786', '-0.01872', '-0.1512', '-0.2101', '-0.00979', '-0.41', '0.01394', '-0.03522', '-0.1164', '0.1261', '0.159', '0.1549', '0.012436', '-0.1752', '-0.1133', '-0.06555', '0.1107', '0.11', '0.1881', '-0.2646', '-0.0325', '-0.00543', '-0.366', '-0.1666', '-0.004025', '-0.00533', '0.06143', '-0.2996', '0.1311', '0.6025', '0.05228', '-0.1396', '-0.3574', '0.1648', '0.0464', '0.07446', '0.0146', '0.3447', '0.1083', '-0.2644', '0.0502', '-0.4353', '0.7046', '-0.1001', '-0.3225', '0.05588', '0.365', '-0.1472', '0.3044', '0.2273', '-0.8545', '0.004547', '0.2942', '0.5513', '0.04868', '0.2769', '-0.07', '-0.1537', '0.3142', '0.01703', '0.5645', '0.1842', '0.1832', '0.3345', '-0.04846', '-0.03928', '0.1143', '-0.1587', '0.3572', '0.436', '0.03595', '0.2083', '-0.11224', '0.2905', '0.1803', '0.2737', '0.2861', '0.1503', '0.2386', '0.2452', '0.4443', '0.1061', '0.503', '-0.145', '-0.4426', '0.145']",,,C564926,,H49.4,,
mondo:0016811,renal tubulopathy-encephalopathy-liver failure syndrome,,,,254902,CN202065,"['0.2417', '0.2056', '-0.201', '-0.169', '-0.003914', '-0.5854', '0.05957', '0.3696', '0.2426', '-0.315', '-0.3643', '-0.9644', '-0.2115', '0.264', '0.066', '-0.0863', '-0.4165', '-0.1752', '-0.3438', '-0.646', '-0.1722', '-0.571', '0.649', '-0.08344', '0.0413', '-0.3032', '-0.3027', '-0.3533', '0.3916', '0.02911', '0.519', '-0.135', '0.3816', '0.3772', '-0.1486', '-0.1644', '-0.857', '-0.5967', '-0.158', '0.2722', '-0.1183', '-0.3171', '-0.1313', '0.1411', '0.0591', '-0.3076', '0.03075', '0.1864', '-0.2063', '-0.1621', '0.2152', '0.2369', '-0.2032', '-0.1729', '0.05554', '-0.0174', '0.10406', '-0.5303', '-0.2423', '0.6943', '0.5303', '0.03748', '0.3157', '-0.1184', '-0.2181', '-0.1087', '0.25', '0.4067', '-0.557', '0.524', '0.05646', '-0.10504', '0.0674', '0.231', '-0.0004747', '0.2825', '0.0887', '-0.5005', '-0.1989', '-0.0615', '-0.002357', '0.252', '-0.5396', '-0.1315', '0.02744', '0.2197', '0.4802', '0.01727', '0.5293', '-0.1884', '0.927', '0.04285', '-0.4854', '-0.0141', '0.1046', '0.4424', '-0.014725', '-0.2391', '-0.03055', '-0.1225']",,,,,,,
mondo:0016812,dopa-responsive dystonia,"['DYT-GCH1 (subtype)', 'Segawa^s disease', 'DYT5 dystonia', 'DYT5', 'DYT-SPR (subtype)', 'hereditary progressive dystonia with diurnal fluctuation', 'DYT-TH (subtype)', 'HPD with diurnal fluctuation']",,,255,C1851920,,C116719,,C538007,,,,
mondo:0016814,maternally-inherited Leigh syndrome,"['Subacute necrotizing encephalomyelopathy maternally inherited', 'maternally inherited Leigh syndrome', 'mitochondrial DNA-associated Leigh syndrome', 'Leigh disease, maternally inherited', 'MILS', 'maternally-inherited Leigh disease', 'maternally-inherited infantile subacute necrotizing encephalopathy']",,,255210,,"['-0.465', '0.5703', '-0.1758', '0.05603', '-0.0554', '-0.7344', '-0.0007253', '0.3494', '-0.2812', '0.01921', '-0.3027', '-0.2362', '-0.07825', '-0.1292', '-0.06964', '-0.2822', '-0.2532', '-0.4097', '-0.01186', '-0.767', '0.06256', '-0.337', '0.566', '-0.04807', '0.1852', '0.00847', '-0.2402', '0.068', '-0.05905', '-0.351', '-0.023', '0.432', '0.4387', '0.3218', '-0.29', '-0.0814', '-0.2773', '0.1703', '-0.5454', '-0.04', '0.03473', '-0.4707', '0.1256', '0.208', '-0.3882', '-0.04596', '-0.2659', '0.01682', '0.5503', '0.138', '-0.1659', '0.1284', '-0.1309', '-0.0648', '0.4246', '-0.6255', '0.277', '0.144', '-0.2583', '0.5693', '0.03638', '-0.0833', '0.707', '0.1105', '-0.3203', '0.1598', '0.3718', '0.5156', '-0.869', '0.4255', '-0.4487', '0.1566', '0.2542', '0.602', '0.1887', '0.00394', '0.08984', '-0.03854', '-0.288', '0.2358', '0.3032', '0.12445', '-0.42', '0.265', '0.3328', '0.02019', '0.4373', '0.306', '0.7285', '0.01915', '0.3945', '0.4866', '-0.095', '0.2048', '-0.001132', '0.589', '0.5063', '-0.1304', '0.0701', '0.274']",,,C536035,,,,
mondo:0016815,Leigh syndrome with leukodystrophy,"['Leigh disease with leukodystrophy', 'infantile subacute necrotizing encephalopathy with leukodystrophy']",,,255241,CN202083,,,,,,,,
mondo:0016816,Leigh syndrome with nephrotic syndrome,"['Leigh disease with nephrotic syndrome', 'infantile subacute necrotizing encephalopathy with nephrotic syndrome']",,,255249,CN202084,"['0.598', '-0.1493', '0.2065', '0.10645', '-0.578', '-0.423', '0.2664', '0.155', '-0.4656', '-0.1182', '0.3528', '-0.2318', '-0.651', '0.618', '-0.693', '-0.1987', '0.0908', '0.6475', '0.583', '-0.7744', '0.7295', '-0.892', '0.1595', '0.614', '-0.05942', '-0.3965', '-0.565', '0.2988', '0.04883', '-0.1047', '0.6274', '-0.1835', '1.047', '-0.11975', '-0.4194', '-0.1749', '-0.08374', '0.2339', '0.066', '-0.629', '-0.1393', '0.1095', '-0.2727', '-0.41', '-0.1633', '-0.3235', '0.2517', '-0.05835', '0.07465', '-0.587', '-0.4453', '0.447', '0.922', '-0.6426', '-0.1841', '-0.4067', '0.0666', '0.1978', '-1.009', '-0.267', '-0.5254', '-0.29', '0.1418', '-0.604', '-0.4924', '0.03345', '0.7065', '0.2515', '-0.8906', '0.6074', '-0.584', '0.6743', '0.1909', '-0.2383', '0.1577', '-0.1608', '0.3374', '0.936', '-0.1891', '0.431', '-0.423', '-0.2152', '-0.2903', '0.1118', '0.03033', '-0.3127', '-0.2083', '-0.2825', '0.3381', '0.511', '0.5015', '0.6533', '-0.6636', '-0.1816', '0.1385', '0.633', '-0.473', '-0.4226', '-0.3435', '-0.203']",,,,,,,
mondo:0016817,Meier-Gorlin syndrome,"['ear-patella-short stature syndrome', 'Meier-Gorlin syndrome']",0060306,,2554,,"['-0.1149', '-0.0744', '0.413', '-0.4158', '0.3257', '-0.2532', '-0.02628', '1.064', '-0.4324', '-0.6445', '0.10535', '-0.2021', '-0.0148', '0.2092', '-0.03345', '-0.0247', '0.6455', '0.2217', '-0.3333', '-0.3257', '0.15', '-0.01516', '0.03732', '-0.2812', '0.4', '-0.004204', '-0.4941', '-0.01834', '0.02124', '-0.1307', '0.4944', '-0.3638', '0.407', '0.461', '0.1923', '-0.05725', '-0.1555', '-0.332', '-0.3228', '-0.2615', '0.1357', '0.09', '-0.3535', '-0.3296', '0.0459', '-0.45', '0.1746', '0.585', '-0.0518', '0.1968', '-0.2214', '-0.05856', '0.004116', '0.1401', '-0.3271', '-0.1407', '-0.3066', '-0.2676', '0.10114', '0.05283', '0.2083', '0.3137', '-0.6533', '0.3203', '0.0931', '-0.1497', '0.04028', '0.0825', '-0.1693', '0.1995', '-0.2012', '0.4578', '0.24', '-0.331', '-0.3733', '0.3088', '0.0506', '0.04947', '-0.2443', '0.159', '0.3223', '0.1632', '0.4172', '0.4297', '-0.1087', '0.221', '-0.4236', '0.1809', '0.0881', '0.2153', '-0.3474', '0.5', '-0.004322', '0.1853', '0.734', '0.03925', '0.2313', '-0.4038', '0.419', '-0.04013']",,,C538012,,,10070612,
mondo:0016818,Mikati-Najjar-Sahli syndrome,['microcephaly-hypergonadotropic hypogonadism-short stature syndrome'],,,2558,CN202088,,,,,,,,
mondo:0016819,Moebius syndrome-axonal neuropathy-hypogonadotropic hypogonadism syndrome,,,,2560,C2931024,,,,,,,,
mondo:0016820,Moyamoya disease,"['Moyamoya disease, secondary', 'MYMY', 'Moyamoya disease, primary', 'progressive intracranial arterial occlusion', 'idiopathic Moyamoya disease']",13099,,2573,C0026654,"['0.1266', '0.0643', '-0.529', '-0.272', '-0.352', '-0.2046', '0.9014', '0.3853', '-0.5356', '-0.57', '0.06192', '-0.07776', '0.4983', '0.4395', '0.471', '0.03043', '-0.338', '-0.12366', '0.4573', '-0.5293', '-0.0812', '0.1487', '0.1531', '-0.2018', '-1.029', '-0.5996', '-0.5835', '0.283', '-0.27', '0.24', '0.02162', '-0.7246', '0.729', '-0.0916', '-0.01133', '-0.0363', '0.1168', '-0.2164', '0.03195', '-1.067', '0.5854', '0.295', '0.1305', '-0.52', '0.649', '0.2214', '-0.2747', '0.15', '-0.1354', '0.01292', '-0.08527', '0.497', '-0.4387', '-0.5845', '0.4702', '0.4956', '-0.4246', '0.3955', '-0.3506', '0.3513', '-0.5693', '0.1248', '0.1898', '-0.2866', '0.08575', '0.4722', '-0.3433', '0.6934', '-0.9575', '0.5586', '-0.2598', '0.00859', '0.01799', '-0.3638', '0.756', '0.523', '0.07416', '0.01918', '0.2034', '-0.2927', '-0.3489', '-0.758', '0.2109', '0.007744', '0.3865', '-0.726', '0.5464', '0.423', '0.8257', '-0.1548', '0.1613', '-0.2642', '0.0356', '-0.3513', '1.19', '-0.5767', '-0.808', '-0.3286', '-0.5537', '0.004234']",C84895,,D009072,437.5,,10028047,
mondo:0016821,shoulder and girdle defects-familial intellectual disability syndrome,"['shoulder girdle defect intellectual disability familial', 'shoulder girdle defect mental retardation familial']",,,2580,CN227007,,,,,,,,
mondo:0016822,myalgia-eosinophilia syndrome associated with tryptophan,,,,2582,,,,,D016603,,,10014952,
mondo:0016823,mycetoma,['Madura foot'],,,2583,C0024449,,C85505,,D008271,,B47,10028427,
mondo:0016824,infantile myofibromatosis,"['IMS', 'infantile myofibromatosis', 'myofibromatosis', 'infantile hemangiopericytoma', 'multicentric myofibromatosis']",0080109,,2591,C0206648,"['0.0807', '0.1956', '0.5347', '-0.2244', '-0.2065', '-0.04367', '0.328', '0.1075', '-0.542', '-0.762', '0.02084', '0.4658', '0.0904', '0.3716', '0.1962', '0.03888', '-0.6436', '-0.62', '0.2778', '-0.3787', '-0.1263', '-0.1599', '0.789', '-0.741', '-0.1796', '-0.1439', '0.08716', '-0.1853', '-0.3596', '-0.1222', '0.3494', '0.12115', '-0.1832', '0.10675', '-0.185', '0.11725', '-0.00906', '0.1082', '0.3604', '0.1353', '0.2054', '-0.5938', '0.4521', '-0.3022', '0.561', '-0.01572', '-0.6904', '0.02844', '0.06836', '0.2598', '0.0665', '0.03372', '0.2484', '0.1089', '-0.25', '-0.0357', '0.1353', '0.0853', '-0.508', '0.3289', '0.1699', '0.2554', '-0.725', '-0.05792', '-0.03003', '-0.2832', '0.5215', '0.647', '0.03952', '0.272', '0.4956', '-0.2888', '0.1968', '-0.1849', '0.6855', '0.0798', '-0.1018', '0.2399', '-0.3845', '-1.239', '-0.3035', '-0.02086', '0.2181', '0.1343', '-0.5566', '-0.3298', '-0.02397', '0.0878', '0.026', '-0.521', '0.7993', '0.1898', '0.266', '-0.4495', '0.5586', '-0.11993', '0.5044', '-0.516', '0.4575', '0.000606']",C3742,,D018224,,,,
mondo:0016825,mitochondrial myopathy-lactic acidosis-deafness syndrome,"['mitochondrial myopathy with lactic acidosis', 'MMLA', 'mitochondrial myopathy-lactic acidosis-hearing loss syndrome', 'metabolic myopathy associated with chronic lactic acidemia, growth failure, and nerve deafness']",,251950,2597,,"['-0.428', '-0.04617', '-0.05823', '-0.00229', '0.1334', '-0.451', '-0.2272', '0.799', '-0.0826', '-0.04364', '-0.3518', '-0.23', '0.0845', '-0.0982', '-0.1199', '0.09534', '0.1234', '0.1169', '-0.4795', '-0.531', '-0.098', '-0.3162', '0.1355', '-0.1035', '0.11975', '-0.1694', '-0.0467', '0.0481', '-0.115', '-0.2057', '0.1788', '0.1318', '0.2494', '0.2396', '-0.2291', '-0.2356', '-0.175', '-0.288', '-0.1227', '-0.00795', '-0.01807', '-0.3179', '0.088', '-0.2046', '0.01779', '-0.0612', '-0.1464', '0.1526', '-0.1576', '0.03094', '-0.1714', '-0.3228', '0.2383', '-0.1021', '0.1096', '-0.2354', '0.3123', '-0.3052', '-0.2019', '0.245', '0.10376', '-0.10016', '0.1246', '-0.2252', '-0.3823', '-0.0814', '0.0601', '0.5117', '-0.5986', '0.2189', '-0.1534', '0.004185', '-0.0856', '-0.0425', '0.3596', '0.02898', '0.0733', '-0.0667', '-0.08704', '0.3862', '0.4182', '0.11865', '-0.04767', '0.2068', '0.2169', '0.376', '0.1619', '0.2137', '0.307', '-0.03302', '0.694', '0.2396', '-0.02295', '-0.03342', '0.432', '0.2253', '0.3975', '-0.524', '-0.02588', '0.01845']",,,C537476,,,,
mondo:0016826,methylmalonic aciduria and homocystinuria,"['methylmalonic acidemia and homocystinemia', 'combined defect in adenosylcobalamin and methylcobalamin synthesis', 'methylmalonic aciduria with homocystinuria']",,,26,,"['0.5557', '0.4907', '0.359', '-0.3735', '-0.008255', '-0.5103', '-0.5103', '0.553', '-0.6074', '0.4934', '-0.574', '-0.2673', '-0.3271', '-0.1931', '-0.0625', '-0.2286', '-0.1603', '-0.5645', '-0.9883', '-0.3254', '0.299', '-0.2097', '-0.002804', '-0.528', '0.448', '0.00271', '0.1526', '-0.2262', '0.2576', '-0.1698', '-0.2002', '0.4133', '0.4897', '0.3545', '-0.02419', '0.4785', '-0.3745', '-0.72', '-0.0001409', '0.1963', '0.3574', '-0.575', '0.4238', '-0.03333', '-0.644', '-0.3264', '0.007214', '-0.7363', '-0.2391', '-0.04935', '-0.2512', '-0.03888', '-0.3486', '-0.1344', '-0.2428', '0.011345', '0.4321', '0.4788', '-0.651', '0.5444', '0.1515', '0.09753', '0.1862', '-0.3994', '-0.3374', '0.2068', '0.4177', '0.4182', '-0.301', '0.641', '0.04373', '0.1366', '-0.8853', '-0.2778', '-0.09784', '0.03476', '0.02357', '-1.274', '-0.1929', '0.0961', '0.4548', '-0.733', '-0.4211', '0.2151', '0.2573', '0.5527', '-0.1189', '1.008', '0.6616', '0.645', '0.4268', '0.2174', '0.03412', '-0.0645', '0.3687', '0.814', '0.4421', '-0.08057', '0.564', '0.07855']",,,C537359,,,,
mondo:0016827,myopathy-growth delay-intellectual disability-hypospadias syndrome,,,,2601,CN230273,,,,,,,,
mondo:0016828,autosomal recessive sideroblastic anemia,"['ARSA', 'sideroblastic anemia, autosomal recessive', 'congenital sideroblastic anaemia', 'congenital sideroblastic anemia']",,,260305,C4274077,"['-0.09534', '0.5684', '-0.3433', '0.2861', '0.516', '-0.1123', '-0.2319', '0.5684', '0.1272', '-0.614', '0.3743', '0.0723', '0.445', '0.161', '-1.1045', '0.204', '-0.504', '0.0809', '-0.539', '-0.6445', '-0.1116', '-0.6216', '0.10925', '-0.1159', '0.6426', '-0.5054', '0.08923', '-0.4175', '0.6035', '-0.05597', '0.0997', '0.1987', '0.4897', '0.601', '0.1986', '-0.2947', '-0.7817', '-0.532', '0.7207', '-0.01099', '-0.688', '0.2418', '-0.04242', '-0.2815', '-0.5166', '-0.965', '-0.0702', '0.04556', '0.1179', '-0.2488', '0.4915', '0.2478', '0.7876', '-0.3008', '0.6235', '-0.633', '0.1713', '0.2866', '-0.8535', '0.05444', '0.02971', '0.3872', '-0.1714', '-0.615', '0.0665', '-0.001405', '0.2744', '0.7383', '-0.5825', '0.689', '0.7656', '-0.2114', '-0.4458', '-0.6836', '0.4802', '0.863', '0.248', '0.02884', '0.0603', '0.381', '0.1587', '-0.02376', '0.0785', '-0.1785', '0.1246', '-0.287', '-0.4207', '0.3281', '0.511', '-0.2372', '0.8613', '0.3518', '-0.3623', '-0.3323', '0.4236', '0.997', '0.1204', '0.1152', '0.2993', '-0.3682']",,,,,,,
mondo:0016829,familial visceral myopathy,"['hereditary hollow visceral myopathy', 'visceral myopathy familial', 'pseudoobstruction idiopathic intestinal', 'megaduodenum and/or megacystis', 'familial hollow visceral myopathy']",,,2604,CN202146,"['-0.4922', '-0.01659', '0.0601', '-0.1526', '-0.3757', '-0.3232', '0.2227', '0.3557', '-0.3813', '0.1644', '-0.2976', '0.2443', '-0.3066', '0.3555', '-0.5693', '-0.1802', '-0.218', '-0.0582', '-0.0708', '-0.8384', '0.2235', '-0.536', '-0.222', '-0.01892', '0.2205', '0.2556', '0.0995', '0.12463', '-0.06354', '-0.2454', '0.0314', '-0.182', '-0.2158', '-0.04648', '0.08075', '0.02087', '-0.425', '-0.0752', '-0.2803', '0.4136', '-0.4197', '-0.371', '0.2993', '0.03183', '0.2559', '0.1088', '-0.3804', '0.07086', '-0.3687', '0.297', '-0.2703', '0.788', '0.1432', '-0.4238', '0.071', '-0.1655', '0.0884', '-0.08356', '-0.4883', '0.1686', '0.4338', '0.3423', '0.2756', '0.10284', '0.1973', '0.10986', '0.757', '0.4084', '0.05438', '0.671', '-0.1626', '0.006554', '0.07654', '-0.1934', '0.0673', '0.266', '0.182', '0.5024', '0.1729', '-0.089', '-0.09686', '-0.2856', '0.2344', '0.215', '0.0411', '-0.004887', '0.05377', '-0.14', '0.2603', '-0.842', '0.2161', '0.1642', '0.317', '0.03464', '0.7983', '0.59', '0.3313', '-0.341', '-0.01631', '0.1271']",,,,359.89,,,
mondo:0016830,Emery-Dreifuss muscular dystrophy,"['Humeroperoneal neuromuscular disease, (formerly)', 'EDMD', 'scapuloperoneal syndrome, X-linked (formerly)']",11726,,261,C0410189,"['-0.07263', '-0.669', '-0.7324', '-0.1421', '0.2822', '-1.064', '0.604', '0.59', '-1.557', '-0.4763', '0.167', '0.2325', '-0.101', '0.9404', '0.10364', '0.2776', '-1.157', '-0.657', '-0.3508', '-0.872', '0.05475', '0.2496', '0.3674', '0.637', '0.1105', '-0.2452', '0.03378', '-0.3298', '0.3022', '-0.4192', '0.749', '-0.09753', '0.6704', '0.3108', '-0.02235', '-0.2015', '-0.1853', '0.1636', '-0.2417', '-0.4954', '-0.05002', '-0.12146', '0.0952', '0.3943', '-0.2041', '0.631', '0.0282', '0.5845', '-0.3623', '0.4062', '0.528', '-0.2156', '0.509', '-0.7046', '0.12115', '-0.683', '0.4895', '1.013', '-0.2208', '-0.05792', '-0.09546', '0.1306', '0.07947', '0.133', '-0.1398', '-0.098', '0.04138', '0.633', '-0.2323', '-0.3093', '-0.1547', '0.1516', '0.2517', '-0.3525', '0.6562', '0.5337', '-0.02933', '0.11597', '0.1959', '0.0636', '0.3232', '-0.1055', '-0.2708', '0.3215', '-0.1317', '0.10767', '-0.0861', '-0.4001', '0.637', '0.1583', '-0.3904', '0.0892', '0.4624', '0.7886', '-0.1483', '-0.03577', '0.4392', '-0.6616', '-0.05453', '0.2522']",C84685,,D020389,,,,
mondo:0016831,linear verrucous nevus syndrome,['linear hamartoma syndrome'],,,2611,CN202159,,,,,,,,
mondo:0016832,distal 7q11.23 microduplication syndrome,"['Dup7q11.23D', 'distal trisomy 7q11.23', 'distal dup(7)(q11.23)']",,,261102,CN202160,,,,,,,,
mondo:0016833,14q12 microdeletion syndrome,"['Del(14)(q12)', 'monosomy 14q12']",,,261144,CN202163,,,,,,,,
mondo:0016834,16p11.2p12.2 microduplication syndrome,"['dup(16)(p11.2p12.2)', 'trisomy 16p11.2p12.2', '16p11.2 microduplication syndrome', '16p11.2-p12.2 microduplication syndrome']",,,261204,CN202168,,,,,,,,
mondo:0016835,14q11.2 microduplication syndrome,"['dup(14)(q11.2)', 'trisomy 14q11.2']",,,261229,CN202171,,,,,,,,
mondo:0016836,16p13.11 microdeletion syndrome,"['Del(16)(p13.11)', '16p13.11 recurrent microdeletion (neurocognitive disorder susceptibility locus)', 'monosomy 16p13.11']",,,261236,CN202172,,,,,,,,
mondo:0016837,16p13.11 microduplication syndrome,"['dup(16)(p13.11)', 'trisomy 16p13.11', '16p13.11 recurrent microduplication (neurocognitive disorder susceptibility locus)']",,,261243,CN202173,,,,,,,,
mondo:0016838,16q24.3 microdeletion syndrome,"['monosomy 16q24.3', 'Del(16)(q24.3)', 'chromosome 16q24.3 microdeletion syndrome']",,,261250,CN202174,,,,,,,,
mondo:0016839,distal 17p13.3 microdeletion syndrome,"['distal monosomy 17p13.3', 'distal del(17)(p13.3)']",,,261257,CN202175,,,,,,,,
mondo:0016840,trisomy 17p,"['17p trisomy', 'chromosome 17p duplication', '17p duplication', 'partial trisomy 17p', 'Duplication 17p', 'trisomy type 17p', 'dup(17p)']",,,261290,C0795865,,,,C538048,,,,
mondo:0016841,20p12.3 microdeletion syndrome,"['Del(20)(p12.3)', 'monosomy 20p12.3']",,,261295,CN202180,,,,,,,,
mondo:0016842,paternal 20q13.2q13.3 microdeletion syndrome,"['paternal monosomy 20q13.2-q13.3', 'paternal del(20)(q13.2q13.3)', 'paternal 20q13.2-q13.3 microdeletion syndrome', 'paternal monosomy 20q13.2q13.3']",,,261304,CN202182,,,,,,,,
mondo:0016843,20q13.33 microdeletion syndrome,"['monosomy 20q13.33', 'Del(20)(q13.33)']",,,261311,CN202183,,,,,,,,
mondo:0016844,trisomy 20p,"['Duplication 20p', 'partial trisomy of the short arm of chromosome 20', 'Duplication of 20p', '20p trisomy', '20p duplication', 'trisomy type 20p', 'dup(20p)', 'partial duplication of the short arm of chromosome 20', 'partial trisomy of chromosome 20p', 'trisomy 20p', 'partial trisomy 20p', 'partial duplication of chromosome 20p', 'chromosome 20p duplication']",,,261318,,,,,C535371,758.5,,,
mondo:0016845,21q22.11q22.12 microdeletion syndrome,"['monosomy 21q22.11q22.12', 'monosomy 21q22.11-q22.12', '21q22.11-q22.12 microdeletion syndrome', 'Del(21)(q22.11q22.12)']",,,261323,CN202185,,,,,,,,
mondo:0016846,distal 22q11.2 microduplication syndrome,"['distal dup(22)(q11.2)', 'distal trisomy 22q11.2']",,,261337,CN202187,,,,,,,,
mondo:0016847,trisomy 1q,"['Duplication 1q', 'trisomy type 1q']",,,261344,,,,,,,,,
mondo:0016848,juvenile temporal arteritis,"['JGCA', 'juvenile cranial arteritis', 'juvenile giant cell arteritis', 'JTA', 'non-giant cell granulomatous temporal arteritis with eosinophilia', 'JPMR', 'juvenile polymyalgia rheumatica']",,,26137,C0751547,,,,,,,,
mondo:0016850,atypical Norrie disease due to monosomy Xp11.3,"['atypical Norrie disease due to del(X)(p11.3)', 'atypical Norrie disease due to Xp11.3 microdeletion']",,,261501,CN202196,,,,,,H35.5,,
mondo:0016851,maternal uniparental disomy of chromosome X,"['UPD(X)mat', 'maternal uniparental disomy of chromosome type X']",,,261519,,,,,,,,,
mondo:0016852,paternal uniparental disomy of chromosome X,"['paternal uniparental disomy of chromosome type X', 'UPD(X)pat']",,,261524,,,,,,,,,
mondo:0016853,ring chromosome Y,"['Ring chromosome type Y', 'r(Y)', 'Ring chromosome Y syndrome']",,,261529,,,,,,,,,
mondo:0016854,"49,XXXYY syndrome","['XXXYY syndrome', '49, XXXYY syndrome']",,,261534,CN202197,,,,,,,,
mondo:0016855,Mowat-Wilson syndrome due to monosomy 2q22,"['Hirschsprung disease and intellectual disability due to del(2)(q22)', 'Mowat-Wilson syndrome due to del(2)q(22)', 'Mowat-Wilson syndrome due to monosomy type 2q22', 'Hirschsprung disease and intellectual disability due to monosomy 2q22', 'Hirschsprung disease and intellectual disability due to 2q22 microdeletion', 'Mowat-Wilson syndrome due to 2q22 microdeletion']",,,261537,CN202198,,,,,,,,
mondo:0016856,Mowat-Wilson syndrome due to a ZEB2 point mutation,['Hirschsprung disease and intellectual disability due to a ZEB2 point mutation'],,,261552,CN202199,,,,,,,,
mondo:0016857,blepharophimosis-epicanthus inversus-ptosis due to 3q23 rearrangement syndrome,,,,261559,CN202200,,,,,,,,
mondo:0016858,blepharophimosis-epicanthus inversus-ptosis due to a point mutation syndrome,['blepharophimosis types 1 and 2 due to a point mutation'],,,261572,CN202201,,,,,,,,
mondo:0016859,blepharophimosis-epicanthus inversus-ptosis due to copy number variations,"['blepharophimosis types 1 and 2 due to copy number variations', 'blepharophimosis-epicanthus inversus-ptosis due to a CNV']",,,261579,CN202202,,,,,,,,
mondo:0016860,familial adenomatous polyposis due to 5q22.2 microdeletion,"['FAP due to monosomy 5q22.2', 'colorectal adenomatous polyposis due to monosomy 5q22.2', 'familial polyposis coli due to monosomy 5q22.2', 'familial adenomatous polyposis due to del(5)(q22.2)', 'familial adenomatous polyposis due to monosomy 5q22.2']",,,261584,CN202203,,,,,,,,
mondo:0016861,Alagille syndrome due to 20p12 microdeletion,"['Alagille syndrome due to monosomy 20p12', 'Alagille-Watson syndrome due to monosomy 20p12', 'syndromic bile duct paucity due to monosomy 20p12', 'Alagille syndrome due to del(20)(p12)', 'Arteriohepatic dysplasia due to monosomy 20p12']",,,261600,CN202205,"['-0.07477', '0.1254', '0.0879', '-0.02528', '0.04272', '-0.1338', '0.007774', '0.1354', '-0.07745', '-0.03433', '-0.014694', '-0.004898', '0.0331', '0.02498', '-0.01851', '-0.07196', '-0.01608', '0.002956', '-0.05948', '-0.182', '-0.02177', '-0.02843', '0.0876', '-0.02975', '0.004036', '-0.00995', '-0.05917', '-0.03467', '0.06555', '-0.06616', '0.07874', '0.014946', '0.1456', '0.0322', '0.002811', '-0.08716', '0.008156', '-0.0229', '-0.01134', '-0.1809', '0.014496', '-0.10974', '0.03543', '-0.08887', '-0.02635', '-0.0944', '-0.01556', '0.06168', '0.02496', '0.04007', '-0.05417', '-0.05444', '-0.01636', '-0.003963', '-0.06915', '0.02553', '0.1187', '-0.04337', '-0.1447', '0.03226', '0.06744', '0.077', '0.02565', '0.0355', '0.04385', '0.010704', '0.12024', '0.05927', '-0.1384', '0.1196', '-0.1371', '0.03506', '0.0541', '-0.0644', '0.02165', '0.03687', '0.05045', '-0.0431', '-0.1289', '-0.00395', '0.01221', '0.04636', '-0.05856', '0.138', '-0.00685', '-0.00953', '0.0788', '0.1362', '0.1599', '-0.00971', '0.04623', '0.1133', '-0.0482', '0.0175', '0.227', '0.02133', '0.1105', '-0.1838', '-0.00879', '0.06137']",,,,,,,
mondo:0016862,Alagille syndrome due to a JAG1 point mutation,"['Alagille-Watson syndrome due to a JAG1 point mutation', 'cholestasis with peripheral pulmonary stenosis', 'arteriohepatic dysplasia due to a JAG1 point mutation', 'Alagille-Watson syndrome', 'syndromic bile duct paucity due to a JAG1 point mutation', 'ALGS1', 'Alagille syndrome 1', 'arteriohepatic dysplasia', 'hepatic ductular hypoplasia, syndromatic', 'Alagille syndrome type 1']",,118450,261619,CN202206,"['-0.1409', '0.08545', '0.3281', '-0.13', '0.341', '-0.302', '0.04153', '0.1967', '-0.11414', '-0.2234', '-0.0656', '-0.2142', '0.06354', '0.1799', '-0.1522', '-0.1586', '-0.0876', '-0.08844', '-0.02716', '-0.2461', '0.10297', '-0.057', '0.34', '-0.2323', '0.0917', '0.0408', '-0.0161', '0.2869', '0.3462', '-0.002495', '0.4158', '0.1016', '0.08813', '0.05972', '-0.106', '-0.3423', '-0.1765', '-0.0967', '0.11957', '-0.1747', '-0.0539', '-0.0699', '0.0714', '0.0487', '0.0951', '-0.03128', '0.202', '0.1682', '-0.2367', '-0.01982', '-0.204', '0.1262', '-0.05402', '0.04276', '-0.151', '-0.3179', '0.2358', '0.1514', '-0.129', '0.12134', '0.2045', '0.09', '-0.03595', '-0.133', '0.002285', '-0.2103', '0.408', '0.3735', '-0.2915', '0.1356', '-0.3845', '-0.04855', '0.12115', '-0.2666', '0.04733', '0.0981', '0.221', '0.02036', '-0.1177', '-0.0532', '-0.0838', '-0.236', '-0.1528', '0.104', '-0.3125', '-0.06006', '0.366', '0.11084', '0.01447', '-0.08746', '0.1683', '0.1975', '-0.01707', '0.02783', '0.7134', '-0.05478', '0.2021', '-0.1893', '0.1644', '0.0789']",,,,,,,
mondo:0016863,Okihiro syndrome due to 20q13 microdeletion,"['Duane-radial ray syndrome due to monosomy 20q13', 'Okihiro syndrome due to monosomy 20q13', 'Okihiro syndrome due to del(20)(q13)']",,,261638,CN202208,,,,,,,,
mondo:0016864,Okihiro syndrome due to a point mutation,['Duane-radial ray syndrome due to a point mutation'],,,261647,CN202209,,,,,,,,
mondo:0016865,Kleefstra syndrome due to a point mutation,,,,261652,CN202210,,,,,,,,
mondo:0016866,partial deletion of chromosome 1,"['partial deletion of chromosome type 1', 'partial monosomy of chromosome 1']",,,261766,,,,,,,,,
mondo:0016867,partial deletion of chromosome 2,"['partial deletion of chromosome type 2', 'partial monosomy of chromosome 2']",,,261771,,,,,,,,,
mondo:0016868,partial deletion of chromosome 3,"['partial monosomy of chromosome 3', 'partial deletion of chromosome type 3']",,,261776,,,,,,,,,
mondo:0016869,partial deletion of chromosome 4,"['partial deletion of chromosome type 4', 'partial monosomy of chromosome 4']",,,261781,,,,,,,,,
mondo:0016870,partial deletion of chromosome 5,"['partial deletion of chromosome type 5', 'partial monosomy of chromosome 5']",,,261786,,,,,,,,,
mondo:0016871,partial deletion of chromosome 6,"['partial deletion of chromosome type 6', 'partial monosomy of chromosome 6']",,,261791,,,,,,,,,
mondo:0016872,partial deletion of chromosome 7,"['partial monosomy of chromosome 7', 'partial deletion of chromosome type 7']",,,261796,,,,,,,,,
mondo:0016873,partial deletion of chromosome 8,"['partial deletion of chromosome type 8', 'partial monosomy of chromosome 8']",,,261801,,,,,,,,,
mondo:0016874,partial deletion of chromosome 9,"['partial monosomy of chromosome 9', 'partial deletion of chromosome type 9']",,,261806,,,,,,,,,
mondo:0016875,partial deletion of chromosome 10,['partial monosomy of chromosome 10'],,,261811,,,,,,,,,
mondo:0016876,partial deletion of chromosome 11,"['partial deletion of chromosome type 11', 'partial monosomy of chromosome 11']",,,261816,,,,,,,,,
mondo:0016877,partial deletion of the long arm of chromosome 12,"['partial deletion of chromosome 12q', 'partial deletion of the long arm of chromosome type 12', 'partial monosomy of chromosome 12q', 'partial monosomy of the long arm of chromosome 12']",,,261821,,,,,,,,,
mondo:0016878,partial deletion of chromosome 16,"['partial monosomy of chromosome 16', 'partial deletion of chromosome type 16']",,,261826,,,,,,,,,
mondo:0016879,partial deletion of chromosome 17,"['partial deletion of chromosome type 17', 'partial monosomy of chromosome 17']",,,261831,,,,,,,,,
mondo:0016880,partial deletion of chromosome 18,"['partial monosomy of chromosome 18', 'partial deletion of chromosome type 18']",,,261836,,,,,,,,,
mondo:0016881,partial deletion of chromosome 19,"['partial monosomy of chromosome 19', 'partial deletion of chromosome type 19']",,,261841,,,,,,,,,
mondo:0016882,partial deletion of chromosome 20,"['partial deletion of chromosome type 20', 'partial monosomy of chromosome 20']",,,261846,,,,,,,,,
mondo:0016883,partial deletion of the short arm of chromosome 1,"['1p monosomy', 'partial deletion of chromosome 1p', 'deletion 1p', 'monosomy 1p', 'partial monosomy 1p', 'partial deletion of the short arm of chromosome type 1', 'loss of chromosome 1p', 'del(1p)', '1p deletion', 'chromosome 1p deletion', 'partial monosomy of chromosome 1p', 'partial monosomy of the short arm of chromosome 1']",,,261857,C0795796,,C36501,,C535591,,,,
mondo:0016884,partial deletion of the short arm of chromosome 2,"['partial monosomy of chromosome 2p', 'partial deletion of the short arm of chromosome type 2', 'partial monosomy of the short arm of chromosome 2', 'partial deletion of chromosome 2p']",,,261866,,,,,,,,,
mondo:0016885,partial deletion of the short arm of chromosome 3,"['partial deletion of chromosome 3p', 'partial monosomy of the short arm of chromosome 3', 'partial deletion of the short arm of chromosome type 3', 'partial monosomy of chromosome 3p']",,,261875,,,,,,,,,
mondo:0016887,partial deletion of the short arm of chromosome 5,"['partial monosomy of the short arm of chromosome 5', 'partial deletion of the short arm of chromosome type 5', 'partial deletion of chromosome 5p', 'partial monosomy of chromosome 5p']",,,261893,,,,,,,,,
mondo:0016888,partial deletion of the short arm of chromosome 6,"['partial monosomy of the short arm of chromosome 6', 'partial monosomy of chromosome 6p', 'partial deletion of chromosome 6p', 'partial deletion of the short arm of chromosome type 6']",,,261902,,,,,,,,,
mondo:0016889,partial deletion of the short arm of chromosome 7,"['7p monosomy', 'chromosome 7p deletion', 'partial monosomy 7p', 'partial deletion of the short arm of chromosome type 7', 'partial monosomy of chromosome 7p', '7p deletion', 'partial monosomy of the short arm of chromosome 7', 'partial deletion of chromosome 7p', 'deletion 7p', 'monosomy 7p']",,,261911,,,,,,,,,
mondo:0016890,partial deletion of the short arm of chromosome 8,"['chromosome 8p deletion', 'partial monosomy of chromosome 8p', 'deletion 8p', '8p deletion', 'partial deletion of the short arm of chromosome type 8', 'partial deletion of chromosome 8p', '8p monosomy', 'partial monosomy of the short arm of chromosome 8', 'partial monosomy 8p', 'monosomy 8p']",,,261920,,,,,C537826,,,,
mondo:0016892,partial deletion of the short arm of chromosome 10,"['partial deletion of chromosome 10p', 'partial monosomy of the short arm of chromosome 10', 'partial monosomy of chromosome 10p', 'partial deletion of the short arm of chromosome type 10']",,,261938,C0795836,,,,,,,,
mondo:0016893,partial deletion of the short arm of chromosome 11,"['partial monosomy of the short arm of chromosome 11', 'partial deletion of chromosome 11p', 'partial monosomy of chromosome 11p', 'partial deletion of the short arm of chromosome type 11']",,,261947,,,,,,,,,
mondo:0016894,partial deletion of the short arm of chromosome 16,"['partial deletion of the short arm of chromosome type 16', 'partial monosomy of chromosome 16p', 'partial deletion of chromosome 16p', 'partial monosomy of the short arm of chromosome 16']",,,261956,,,,,,,,,
mondo:0016897,partial deletion of the short arm of chromosome 19,"['partial monosomy of the short arm of chromosome 19', 'partial monosomy of chromosome 19p', 'partial deletion of chromosome 19p', 'partial deletion of the short arm of chromosome type 19']",,,261983,,,,,,,,,
mondo:0016898,partial monosomy of the short arm of chromosome 20,"['partial deletion of the short arm of chromosome 20', 'partial monosomy of chromosome 20p', 'partial monosomy 20p', 'partial deletion of chromosome 20p', 'partial monosomy of the short arm of chromosome type 20', '20p deletion', '20p monosomy', 'Pure partial 20p deletion', 'monosomy 20p', 'deletion 20p', 'chromosome 20p deletion']",,,261992,CN036364,,,,C535370,,,,
mondo:0016899,Duchenne and Becker muscular dystrophy,"['severe dystrophinopathy, Duchenne and Becker type']",,,262,CN227033,,,,,,,,
mondo:0016901,partial deletion of the long arm of chromosome 2,"['partial monosomy of the long arm of chromosome 2', '2q deletion', '2q monosomy', 'partial deletion of chromosome 2q', 'chromosome 2q deletion', 'monosomy 2q', 'partial monosomy 2q', 'partial deletion of the long arm of chromosome type 2', 'deletion 2q', 'partial monosomy of chromosome 2q']",,,262010,C0795804,,,,C538315,,,,
mondo:0016902,partial deletion of the long arm of chromosome 3,"['partial deletion of chromosome 3q', 'partial monosomy of the long arm of chromosome 3', 'partial monosomy of chromosome 3q', 'partial deletion of the long arm of chromosome type 3']",,,262019,,,,,,,,,
mondo:0016903,partial deletion of the long arm of chromosome 4,"['partial deletion of chromosome 4q', 'partial monosomy 4q', 'partial deletion of the long arm of chromosome type 4', 'partial monosomy of the long arm of chromosome 4', 'partial monosomy of chromosome 4q', 'deletion 4q', '4q monosomy', 'chromosome 4q deletion', 'monosomy 4q', '4q deletion']",,,262029,,,,,C537639,,,,
mondo:0016904,partial deletion of the long arm of chromosome 5,"['partial deletion of the long arm of chromosome type 5', 'partial deletion of chromosome 5q', 'partial monosomy of chromosome 5q', 'partial monosomy of the long arm of chromosome 5']",,,262038,,,,,,,,,
mondo:0016905,partial deletion of the long arm of chromosome 6,"['partial deletion of chromosome 6q', 'partial monosomy of the long arm of chromosome 6', 'partial monosomy 6q', '6q deletion', 'partial monosomy of chromosome 6q', 'monosomy 6q', 'deletion 6q', 'chromosome 6q deletion', '6q monosomy', 'partial deletion of the long arm of chromosome type 6']",,,262047,C0795816,,,,C537807,,,,
mondo:0016906,partial deletion of the long arm of chromosome 7,"['loss of chromosome 7q', '7q monosomy', 'del(7q)', 'partial deletion of chromosome 7q', 'partial monosomy of chromosome 7q', 'partial monosomy of the long arm of chromosome 7', 'monosomy 7q', '7q deletion', 'partial monosomy 7q', 'partial deletion of the long arm of chromosome type 7', 'deletion 7q']",,,262056,,,C36408,,,,,,
mondo:0016907,partial deletion of the long arm of chromosome 8,"['partial deletion of chromosome 8q', '8q deletion', 'partial deletion of the long arm of chromosome type 8', 'chromosome 8q deletion', 'monosomy 8q', 'partial monosomy of the long arm of chromosome 8', 'partial monosomy of chromosome 8q', 'partial monosomy 8q', 'deletion 8q', '8q monosomy']",,,262065,C0795828,,,,C537828,,,,
mondo:0016908,partial monosomy of the long arm of chromosome 9,"['partial deletion of chromosome 9q', 'partial monosomy of chromosome 9q', 'partial deletion of the long arm of chromosome 9', 'partial monosomy of the long arm of chromosome type 9']",,,262074,,,,,,,,,
mondo:0016909,partial monosomy of the long arm of chromosome 10,"['partial monosomy of chromosome 10q', 'partial deletion of chromosome 10q', 'partial deletion of the long arm of chromosome 10', 'partial monosomy of the long arm of chromosome type 10']",,,262083,C0795839,,,,,,,,
mondo:0016910,partial deletion of the long arm of chromosome 11,"['11q monosomy', 'partial deletion of the long arm of chromosome type 11', '11q deletion', 'Deletion 11q partial', 'partial monosomy of chromosome 11q', 'chromosome 11q partial deletion', 'del(11q)', 'monosomy 11q partial', 'monosomy 11q', 'partial monosomy of the long arm of chromosome 11', 'partial deletion of chromosome 11q', 'chromosome 11q deletion', 'partial monosomy 11q', 'loss of chromosome 11q', 'deletion 11q']",,,262092,CN035778,,C37312,,C538296,,,,
mondo:0016911,partial deletion of the long arm of chromosome 13,"['loss of chromosome 13q', '13q monosomy', 'partial monosomy of chromosome 13q', 'monosomy 13q', 'chromosome 13q deletion', 'del(13q)', 'partial deletion of the long arm of chromosome type 13', 'partial deletion of chromosome 13q', 'deletion 13q', '13q deletion', 'partial monosomy of the long arm of chromosome 13']",,,262101,,,C36497,,C535449,,,,
mondo:0016912,partial deletion of the long arm of chromosome 14,"['deletion 14q', '14q monosomy', 'partial deletion of the long arm of chromosome type 14', '14q deletion', 'partial deletion of chromosome 14q', 'partial monosomy of chromosome 14q', 'partial monosomy of the long arm of chromosome 14', 'chromosome 14q deletion', 'partial monosomy 14q', 'monosomy 14q']",,,262110,,,,,,,,,
mondo:0016913,partial deletion of the long arm of chromosome 15,"['partial monosomy 15q', 'partial monosomy of chromosome 15q', 'partial monosomy of the long arm of chromosome 15', 'monosomy 15q', 'chromosome 15q deletion', '15q deletion', 'partial deletion of chromosome 15q', 'deletion 15q', 'partial deletion of the long arm of chromosome type 15', '15q monosomy']",,,262119,,,,,C538038,,,,
mondo:0016914,partial deletion of the long arm of chromosome 16,"['partial deletion of chromosome 16q', 'partial deletion of the long arm of chromosome type 16', 'partial monosomy of the long arm of chromosome 16', 'partial monosomy of chromosome 16q']",,,262128,,,,,,,,,
mondo:0016915,partial deletion of the long arm of chromosome 17,"['partial deletion of chromosome 17q', 'partial monosomy of chromosome 17q', 'partial deletion of the long arm of chromosome type 17', 'partial monosomy of the long arm of chromosome 17']",,,262137,,,,,,,,,
mondo:0016917,partial deletion of the long arm of chromosome 19,"['partial monosomy of the long arm of chromosome 19', 'partial deletion of the long arm of chromosome type 19', 'partial deletion of chromosome 19q', 'partial monosomy of chromosome 19q']",,,262155,,,,,,,,,
mondo:0016918,partial deletion of the long arm of chromosome 20,"['partial monosomy of the long arm of chromosome 20', 'partial deletion of the long arm of chromosome type 20', 'partial deletion of chromosome 20q', 'partial monosomy of chromosome 20q']",,,262164,,,,,,,,,
mondo:0016919,partial deletion of the long arm of chromosome 21,"['partial monosomy of chromosome 21q', 'partial deletion of chromosome 21q', 'partial deletion of the long arm of chromosome type 21', 'partial monosomy of the long arm of chromosome 21']",,,262173,,,,,,,,,
mondo:0016921,partial duplication of chromosome 1,"['partial duplication of chromosome type 1', 'partial trisomy of chromosome 1']",,,262191,,,,,,,,,
mondo:0016922,partial duplication of chromosome 2,"['partial trisomy of chromosome 2', 'partial duplication of chromosome type 2']",,,262196,,,,,,,,,
mondo:0016923,partial duplication of chromosome 3,"['partial trisomy of chromosome 3', 'partial duplication of chromosome type 3']",,,262201,,,,,,,,,
mondo:0016924,partial duplication of chromosome 4,"['partial duplication of chromosome type 4', 'partial trisomy of chromosome 4']",,,262206,,,,,,,,,
mondo:0016925,partial trisomy/tetrasomy of chromosome 5,"['partial duplication/triplication of chromosome 5', 'partial trisomy/tetrasomy of chromosome type 5']",,,262211,,,,,,,,,
mondo:0016927,partial duplication of chromosome 6,"['partial trisomy of chromosome 6', 'partial duplication of chromosome type 6']",,,262628,,,,,,,,,
mondo:0016928,partial duplication of chromosome 7,"['partial duplication of chromosome type 7', 'partial trisomy of chromosome 7']",,,262633,,,,,,,,,
mondo:0016929,partial duplication of chromosome 8,"['partial trisomy of chromosome 8', 'partial duplication of chromosome type 8']",,,262638,,,,,C537941,,,,
mondo:0016930,partial trisomy/tetrasomy of chromosome 9,"['partial trisomy/tetrasomy of chromosome type 9', 'partial duplication/triplication of chromosome 9']",,,262643,,,,,,,,,
mondo:0016931,partial duplication of chromosome 10,['partial trisomy of chromosome 10'],,,262648,,,,,,,,,
mondo:0016932,partial duplication of chromosome 11,"['partial duplication of chromosome type 11', 'partial trisomy of chromosome 11']",,,262653,,,,,,,,,
mondo:0016933,partial trisomy/tetrasomy of the short arm of chromosome 12,"['partial duplication/triplication of chromosome 12p', 'partial trisomy/tetrasomy of the short arm of chromosome type 12', 'partial duplication/triplication of the short arm of chromosome 12', 'partial trisomy/tetrasomy of chromosome 12p']",,,262658,,,,,,,,,
mondo:0016934,partial duplication of chromosome 16,"['partial trisomy of chromosome 16', 'partial duplication of chromosome type 16']",,,262672,,,,,,,,,
mondo:0016935,partial duplication of chromosome 17,"['partial duplication of chromosome type 17', 'partial trisomy of chromosome 17']",,,262677,C4518505,,,,,,,,
mondo:0016936,partial trisomy/tetrasomy of chromosome 18,"['partial trisomy/tetrasomy of chromosome type 18', 'partial duplication/triplication of chromosome 18']",,,262682,,,,,,,,,
mondo:0016937,partial duplication of chromosome 19,"['partial duplication of chromosome type 19', 'partial trisomy of chromosome 19']",,,262687,,,,,,,,,
mondo:0016938,partial trisomy of chromosome 20,"['partial duplication of chromosome 20', 'partial trisomy of chromosome type 20']",,,262692,C4518509,,,,,,,,
mondo:0016939,partial duplication of the short arm of chromosome 2,"['2p trisomy', 'partial duplication of chromosome 2p', 'trisomy 2p', 'chromosome 2p duplication', 'Duplication 2p', 'partial trisomy 2p', '2p duplication', 'partial duplication of the short arm of chromosome type 2', 'partial trisomy of chromosome 2p']",,,262698,C0795803,,,,C538318,,,,
mondo:0016940,partial duplication of the short arm of chromosome 3,"['partial trisomy of chromosome 3p', 'partial duplication of chromosome 3p', '3p duplication', 'chromosome 3p duplication', '3p trisomy', 'partial trisomy 3p', 'Duplication 3p', 'trisomy 3p', 'partial trisomy of the short arm of chromosome 3', 'partial duplication of the short arm of chromosome type 3']",,,262707,,,,,C536811,,,,
mondo:0016941,partial duplication of the short arm of chromosome 4,"['partial duplication of chromosome 4p', 'partial trisomy of chromosome 4p', 'partial duplication of the short arm of chromosome type 4', 'partial trisomy of the short arm of chromosome 4']",,,262716,,,,,,,,,
mondo:0016942,partial trisomy/tetrasomy of the short arm of chromosome 5,"['partial trisomy/tetrasomy of chromosome 5p', 'partial duplication/triplication of the short arm of chromosome 5', 'partial duplication/triplication of chromosome 5p', 'partial trisomy/tetrasomy of the short arm of chromosome type 5']",,,262725,,,,,,,,,
mondo:0016943,partial duplication of the short arm of chromosome 6,"['partial duplication of the short arm of chromosome type 6', 'partial trisomy of the short arm of chromosome 6', 'chromosome 6p duplication', 'partial duplication of chromosome 6p', '6p trisomy', 'partial trisomy 6p', 'Duplication 6p', 'partial trisomy of chromosome 6p', '6p duplication', 'trisomy 6p']",,,262740,CN036641,,,,C537811,,,,
mondo:0016944,partial duplication of the short arm of chromosome 7,"['partial duplication of the short arm of chromosome type 7', 'partial trisomy of the short arm of chromosome 7', '7p trisomy', 'Duplication 7p', '7p duplication', 'trisomy 7p', 'partial trisomy 7p', 'partial duplication of chromosome 7p', 'chromosome 7p duplication', 'partial trisomy of chromosome 7p']",,,262749,C0795820,,,,C537819,,,,
mondo:0016945,partial duplication of the short arm of chromosome 8,"['chromosome 8p duplication', 'partial trisomy 8p', '8p duplication', 'partial trisomy of chromosome 8p', 'Duplication 8p', 'partial trisomy of the short arm of chromosome 8', 'partial duplication of chromosome 8p', 'trisomy 8p', 'partial duplication of the short arm of chromosome type 8', '8p trisomy']",,,262758,,,,,,,,,
mondo:0016947,partial duplication of the short arm of chromosome 10,"['partial trisomy of the short arm of chromosome 10', 'partial duplication of chromosome 10p', 'partial trisomy of chromosome 10p']",,,262776,,,,,,,,,
mondo:0016948,partial duplication of the short arm of chromosome 11,"['partial trisomy of chromosome 11p', 'partial duplication of chromosome 11p', 'partial trisomy of the short arm of chromosome 11', 'partial duplication of the short arm of chromosome type 11']",,,262785,,,,,,,,,
mondo:0016949,partial duplication of the short arm of chromosome 16,"['Duplication 16p', 'partial duplication of the short arm of chromosome type 16', '16p duplication', 'chromosome 16p duplication', 'partial duplication of chromosome 16p', 'partial trisomy of chromosome 16p', 'partial trisomy of the short arm of chromosome 16', '16p trisomy', 'trisomy 16p', 'partial trisomy 16p']",,,262794,C0795861,,,,,,,,
mondo:0016950,partial duplication of the short arm of chromosome 17,"['partial trisomy of chromosome 17p', 'partial trisomy of the short arm of chromosome 17', 'partial duplication of the short arm of chromosome type 17', 'partial duplication of chromosome 17p']",,,262803,,,,,,,,,
mondo:0016951,partial trisomy/tetrasomy of the short arm of chromosome 18,"['partial trisomy/tetrasomy of chromosome 18p', 'partial trisomy/tetrasomy of the short arm of chromosome type 18', 'partial duplication/triplication of chromosome 18p', 'partial duplication/triplication of the short arm of chromosome 18']",,,262812,,,,,,,,,
mondo:0016952,partial duplication of the long arm of chromosome 1,"['partial trisomy 1q', 'partial trisomy of chromosome 1q', 'partial duplication of chromosome 1q', 'partial trisomy of the long arm of chromosome 1', 'partial duplication of the long arm of chromosome type 1', '1q duplications']",,,262833,C0795800,,C36521,,,,,,
mondo:0016953,partial duplication of the long arm of chromosome 2,"['partial trisomy 2q', 'partial duplication of chromosome 2q', 'trisomy 2q', 'Duplication 2q', 'partial trisomy of chromosome 2q', 'partial duplication of the long arm of chromosome type 2', '2q duplication', '2q trisomy', 'partial trisomy of the long arm of chromosome 2', 'chromosome 2q duplication']",,,262842,C0795805,,,,C535367,,,,
mondo:0016954,partial duplication of the long arm of chromosome 3,"['chromosome 3q duplication', 'partial duplication of the long arm of chromosome type 3', 'partial duplication of chromosome 3q', 'trisomy 3q', 'chromosome 3, trisomy 3q', 'partial trisomy of chromosome 3q', 'Duplication 3q']",,,262851,C0795809,,,,C536813,,,,
mondo:0016955,partial duplication of the long arm of chromosome 4,"['partial trisomy of the long arm of chromosome 4', 'Duplication 4q syndrome, partial', 'chromosome 4q duplication', 'partial duplication of the long arm of chromosome type 4', 'chromosome 4, partial trisomy 4q', 'partial trisomy of chromosome 4q', '4q trisomy', 'partial trisomy distal 4q', 'trisomy 4q', 'partial trisomy 4q syndrome', '4q duplication', 'Duplication 4q', 'partial duplication of chromosome 4q', 'dup(4q) syndrome, partial', 'partial trisomy 4q', 'distal 4q trisomy']",0111159,,262860,C0795812,,,,C537644,,,,
mondo:0016956,partial trisomy of the long arm of chromosome 5,"['partial duplication of the long arm of chromosome 5', 'partial trisomy of the long arm of chromosome type 5', 'trisomy 5q', 'partial trisomy 5q', '5q duplication', 'partial duplication of chromosome 5q', 'chromosome 5q duplication', '5q trisomy', 'partial trisomy of chromosome 5q', 'Duplication 5q']",,,262869,C1802398,,,,C537650,,,,
mondo:0016957,partial duplication of the long arm of chromosome 6,"['partial trisomy of chromosome 6q', 'partial trisomy of the long arm of chromosome 6', 'chromosome 6q duplication', 'partial duplication of chromosome 6q', 'partial trisomy 6q', 'partial duplication of the long arm of chromosome type 6', '6q duplication', 'Duplication 6q', '6q trisomy', 'trisomy 6q']",,,262878,,,,,C537812,,,,
mondo:0016958,partial duplication of the long arm of chromosome 7,"['7q duplication', 'partial trisomy of chromosome 7q', 'partial duplication of chromosome 7q', 'Duplication 7q', 'trisomy 7q', 'partial trisomy of the long arm of chromosome 7', '7q trisomy', 'chromosome 7q duplication', 'partial duplication of the long arm of chromosome type 7', 'partial trisomy 7q']",,,262887,C0795821,,,,C537821,,,,
mondo:0016959,partial duplication of the long arm of chromosome 8,"['partial trisomy of the long arm of chromosome 8', 'partial duplication of the long arm of chromosome type 8', 'partial duplication of chromosome 8q', 'partial trisomy of chromosome 8q']",,,262896,,,,,,,,,
mondo:0016960,partial trisomy of the long arm of chromosome 9,"['partial duplication of chromosome 9q', 'partial trisomy of the long arm of chromosome type 9', 'partial trisomy of chromosome 9q', 'partial duplication of the long arm of chromosome 9']",,,262905,,,,,,,,,
mondo:0016961,partial duplication of the long arm of chromosome 10,"['partial trisomy of the long arm of chromosome 10', 'partial trisomy of chromosome 10q', 'partial duplication of chromosome 10q']",,,262914,,,,,,,,,
mondo:0016964,partial duplication of the long arm of chromosome 14,"['14q trisomy', 'partial duplication of the long arm of chromosome type 14', 'partial trisomy of chromosome 14q', 'partial trisomy 14q', 'Duplication 14q', '14q duplication', 'partial trisomy of the long arm of chromosome 14', 'chromosome 14q duplication', 'partial duplication of chromosome 14q', 'trisomy 14q']",,,262941,,,,,,,,,
mondo:0016965,partial duplication of the long arm of chromosome 15,"['partial duplication of chromosome 15q', 'trisomy 15q', 'partial trisomy 15q', 'partial duplication of the long arm of chromosome type 15', 'partial trisomy of chromosome 15q', 'partial trisomy of the long arm of chromosome 15', 'chromosome 15q duplication', 'Duplication 15q', '15q duplication', '15q trisomy']",,,262950,C0795858,,,,C538040,,,,
mondo:0016966,partial trisomy of the long arm of chromosome 16,"['16q trisomy', 'partial trisomy of the long arm of chromosome type 16', 'partial duplication of the long arm of chromosome 16', 'chromosome 16q duplication', 'Duplication 16q', '16q duplication', 'partial trisomy 16q', 'trisomy 16q', 'partial trisomy of chromosome 16q', 'partial duplication of chromosome 16q']",,,262959,CN036363,,,,C538042,,,,
mondo:0016967,partial duplication of the long arm of chromosome 17,"['trisomy 17q', '17q trisomy', 'partial trisomy of chromosome 17q', 'partial trisomy of the long arm of chromosome 17', 'chromosome 17q duplication', '17q duplication', 'partial trisomy 17q', 'partial duplication of chromosome 17q', 'Duplication 17q', 'partial duplication of the long arm of chromosome type 17']",,,262968,CN035860,,,,,,,,
mondo:0016968,partial trisomy of the long arm of chromosome 18,"['18q trisomy', 'partial duplication of the long arm of chromosome 18', 'partial trisomy of chromosome 18q', 'Duplication 18q', '18q duplication', '18q partial trisomy', 'chromosome 18q duplication', 'partial trisomy of the long arm of chromosome type 18', 'partial duplication of chromosome 18q', 'trisomy 18q']",,,262977,C0809935,,,,C538308,,,,
mondo:0016969,partial duplication of the long arm of chromosome 19,"['trisomy 19q', 'partial trisomy 19q', 'Duplication 19q', 'chromosome 19q duplication', '19q duplication', 'partial duplication of chromosome 19q', '19q trisomy', 'partial trisomy of chromosome 19q', 'partial trisomy of the long arm of chromosome 19', 'partial duplication of the long arm of chromosome type 19']",,,262986,C0795871,,,,C538311,,,,
mondo:0016970,partial trisomy of the long arm of chromosome 20,"['partial trisomy of the long arm of chromosome type 20', 'partial duplication of the long arm of chromosome 20', 'partial trisomy of chromosome 20q', 'partial duplication of chromosome 20q']",,,262995,,,,,,,,,
mondo:0016971,limb-girdle muscular dystrophy,"['erb^s muscular dystrophy', 'Leyden-Mobius muscular dystrophy', 'Leyden-Mbius muscular dystrophy', 'LGMD', 'limb girdle muscular dystrophy']",11724,,263,C0686353,,C84828,,D049288,,,,
mondo:0016972,partial duplication of the long arm of chromosome 22,"['partial duplication of chromosome 22q', 'partial trisomy of the long arm of chromosome 22', 'partial trisomy of chromosome 22q', 'partial duplication of the long arm of chromosome type 22']",,,263004,,,,,,,,,
mondo:0016974,thymoma type B,"['plump cell thymoma', 'primary thymic epithelial neoplasm type B', 'epithelioid thymoma', 'primary thymic epithelial tumor type B', 'Dendritic cell thymoma', 'dendritic cell thymoma', 'thymoma type B', 'dendritic cell thymoma (disease)', 'primary thymic epithelial tumour type B']",3282,,263317,CN202276,,C7114,,,,D15.0,,
mondo:0016975,thymoma type AB,"['primary thymic epithelial tumour type AB', 'primary thymic epithelial tumor type AB', 'primary thymic epithelial neoplasm type AB', 'thymoma type AB', 'thymoma, mixed type', 'mixed type thymoma']",3280,,263324,C1266092,,C6885,1000582,,,D15.0,,
mondo:0016976,well-differentiated thymic neuroendocrine carcinoma,,,,263331,CN202278,,,,,,,,
mondo:0016977,moderately-differentiated thymic neuroendocrine carcinoma,,,,263335,CN202279,,,,,,,,
mondo:0016978,poorly differentiated thymic neuroendocrine carcinoma,,,,263339,CN202280,,,,,,,,
mondo:0016979,MRCS syndrome,['microcornea-rod-cone dystrophy-cataract-posterior staphyloma syndrome'],,,263347,,"['-0.544', '-0.0801', '0.05865', '0.09576', '0.2374', '-0.278', '0.05695', '0.257', '-0.2429', '-0.0727', '-0.2388', '-0.2166', '-0.3245', '-0.00935', '-0.1855', '-0.2058', '0.4836', '-0.06555', '0.01932', '-0.7153', '-0.1995', '0.03564', '0.02805', '0.0778', '-0.05768', '-0.02965', '-0.3582', '0.10834', '0.03302', '0.3682', '0.4834', '0.1764', '0.3086', '0.3667', '-0.0376', '-0.04257', '0.1267', '-0.03069', '-0.2495', '-0.4297', '0.354', '-0.015045', '0.03342', '0.0164', '-0.11646', '0.1681', '-0.05862', '0.07135', '0.04474', '0.1997', '0.0876', '0.2156', '0.2266', '-0.3123', '0.0866', '-0.26', '0.5195', '-0.00936', '-0.3557', '-0.02777', '0.1278', '-0.148', '0.07086', '0.1499', '0.0726', '-0.07367', '0.5317', '0.6147', '-0.1215', '0.4644', '-0.4739', '0.101', '0.1255', '-0.22', '0.1713', '-0.4185', '0.3877', '-0.2098', '-0.12177', '-0.04205', '0.2588', '-0.158', '-0.1002', '0.7295', '-0.12476', '-0.10095', '-0.04065', '0.2532', '0.3928', '0.194', '0.0769', '0.47', '-0.01886', '-0.02615', '0.5894', '-0.1362', '0.2742', '0.047', '0.0838', '0.281']",,,,,,,
mondo:0016980,ATR-X-related syndrome,,,,263355,CN202282,,,,,,,,
mondo:0016981,infantile spams-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome,['infantile spasms-psychomotor retardation-progressive brain atrophy-basal ganglia disease syndrome'],,,263410,CN202284,,,,,,,,
mondo:0016982,angiosarcoma,"['hemangiosarcoma, malignant', 'angiosarcoma', 'hemangiosarcoma', 'malignant hemangioendothelioma', 'angiosarcoma (disease)', 'sarcoma of blood vessel', 'malignant angioendothelioma']",0001816,,263413,C0018923,,C3088,0003968,D006394,171.9,,10002476,0200058
mondo:0016983,Bartter syndrome with hypocalcemia,"['Bartter syndrome type V', 'Bartter syndrome type 5']",,,263417,C3715128,,,,,,,,
mondo:0016984,nevus of Ota,"['Ota^s Nevus', 'oculocutaneous melanocytic Nevus', 'Nevus fusculoceruleus ophthalmomaxillaris', 'oculodermal melanocytosis']",,,263425,C0027961,,C7583,1000396,D009507,224.0,,10051713,
mondo:0016985,nevus of Ito,"['nevus fuscocaeruleus acromiodeltoideus', 'Ito^s Nevus', 'nevi of Ito', 'hypomelanosis of Ito']",,,263432,CN202288,,C7582,1000395,,,,,
mondo:0016986,congenital smooth muscle hamartoma,,,,263435,C0406819,,,,,759.6,,,
mondo:0016987,neuroacanthocytosis,['neuroacanthocytosis syndrome'],0050765,,263440,,,C84926,,D054546,,,,
mondo:0016988,hyperinsulinism due to HNF4A deficiency,['hyperinsulinemic hypoglycemia due to HNF4A deficiency'],,,263455,C4274078,,,,,,,,
mondo:0016989,Fuchs heterochromic iridocyclitis,"['Fuchs^ heterochromic uveitis', 'Fuch^s heterochromic iridocyclitis', 'Fuchs uveitis syndrome', 'Fuchs heterochromic uveitis', 'FHI', 'Fuchs^ heterochromic cyclitis', 'Fuchs heterochromic cyclitis']",9375,,263479,C0016782,,,,,364.21,,10017406,
mondo:0016990,acquired prothrombin deficiency,"['hypoprothrombinemia, acquired', 'acquired prothrombin deficiency', 'acquired hypoprothrombinemia', 'acquired factor II deficiency']",,,26348,C0392610,,C131622,,C538174,,,,
mondo:0016991,acute necrotizing encephalopathy of childhood,"['isolated acute necrotizing encephalopathy', 'isolated ANE', 'ANEC']",,,263524,,,,,,,,,
mondo:0016993,generalized peeling skin syndrome type C,"['peeling skin syndrome type C', 'generalised deciduous skin type C', 'generalized deciduous skin type C']",,,263558,CN202307,,,,,,,,
mondo:0016994,microcephalic osteodysplastic primordial dwarfism types I and III,"['microcephalic osteodysplastic primordial dwarfism type 1', 'osteodysplastic primordial dwarfism type I', 'MOPD types I and III', 'primordial microcephalic dwarfism, Crachami type', 'Brachymelic primordial dwarfism', 'MOPD 1', 'microcephalic osteodysplastic primordial dwarfism, Taybi-Linder type', 'microcephalic osteodysplastic primordial dwarfism types 1 and 3', 'Taybi-Linder syndrome', 'Cephaloskeletal dysplasia', 'low-birth-weight dwarfism with skeletal dysplasia']",,,2636,CN202308,,,,,,,,
mondo:0016995,familial multiple meningioma,,,,263662,CN202309,,,,,,,,
mondo:0016996,NK-cell enteropathy,,,,263665,C4509932,,,,,,,,
mondo:0017003,partial deletion of chromosome X,"['partial deletion of chromosome type X', 'partial monosomy of chromosome X']",,,263726,,,,,,,,,
mondo:0017004,partial monosomy of the short arm of chromosome X,"['partial deletion of chromosome Xp', 'partial monosomy of chromosome Xp', 'partial deletion of the short arm of chromosome X', 'partial monosomy of the short arm of chromosome type X']",,,263731,,,,,,,,,
mondo:0017007,partial deletion of the long arm of chromosome X,"['partial monosomy of the long arm of chromosome X', 'partial deletion of chromosome Xq', 'partial monosomy of chromosome Xq', 'partial deletion of the long arm of chromosome type X']",,,263756,,,,,,,,,
mondo:0017008,partial duplication of chromosome X,"['partial duplication of chromosome type X', 'partial trisomy of chromosome X']",,,263768,,,,,,,,,
mondo:0017009,partial duplication of the short arm of chromosome X,"['partial trisomy of the short arm of chromosome X', 'partial duplication of the short arm of chromosome type X', 'partial duplication of chromosome Xp', 'partial trisomy of chromosome Xp']",,,263775,,,,,,,,,
mondo:0017010,partial duplication of the long arm of chromosome X,"['Xq trisomy', 'partial trisomy of the long arm of chromosome X', 'chromosome Xq duplication', 'partial duplication of chromosome Xq', 'partial trisomy Xq', 'trisomy Xq', 'Xq duplication', 'partial trisomy of chromosome Xq', 'partial duplication of the long arm of chromosome type X', 'Duplication Xq']",,,263783,C0795891,,,,C536732,,,,
mondo:0017012,partial duplication of the short arm of chromosome 1,"['partial trisomy of chromosome 1p', 'partial duplication of chromosome 1p', 'partial duplication of the short arm of chromosome type 1']",,,264431,,,,,,,,,
mondo:0017013,trisomy 8p,"['Duplication 8p', 'trisomy type 8p']",,,264450,,,,,C538019,,,,
mondo:0017014,interstitial lung disease specific to childhood,"['ILD specific to childhood', 'pediatric interstitial lung disease', 'chILD syndrome', 'paediatric interstitial lung disease', 'interstitial lung disease of childhood', 'chILD']",,,264656,CN202324,,,,,,,,
mondo:0017015,primary interstitial lung disease specific to childhood,"['child', 'primary interstitial lung disease specific to childhood', 'children^s interstitial lung disease', 'primary ILD specific to childhood']",,,264665,CN202326,,,,,,,,
mondo:0017018,isolated pulmonary capillaritis,,,,264691,C3873357,,,,,448.9,,,
mondo:0017019,interstitial lung disease specific to infancy,['ILD specific to infancy'],,,264694,CN202332,,,,,,,,
mondo:0017025,Langerhans cell histiocytosis specific to childhood,"['childhood Langerhans cell histiocytosis', 'Langerhans cell histiocytosis', 'Langerhans cell granulomatosis specific to childhood', 'histiocytosis X specific to childhood']",,,264724,C3899655,,C114483,,,,,,
mondo:0017026,interstitial lung disease specific to adulthood,['ILD specific to adulthood'],,,264735,CN202338,,,,,,,,
mondo:0017027,primary interstitial lung disease specific to adulthood,['primary ILD specific to adulthood'],,,264740,CN202339,,,,,,,,
mondo:0017029,Langerhans cell histiocytosis specific to adulthood,"['Langerhans cell histiocytosis', 'histiocytosis X specific to adulthood', 'Langerhans cell granulomatosis specific to adulthood', 'adult Langerhans cell histiocytosis']",,,264750,C3900100,,C114929,,,,,,
mondo:0017030,interstitial lung disease in childhood and adulthood,['ILD in childhood and adulthood'],,,264757,CN202341,,,,,,,,
mondo:0017031,primary interstitial lung disease in childhood and adulthood,['primary ILD in childhood and adulthood'],,,264762,CN202342,,,,,,,,
mondo:0017034,secondary interstitial lung disease in childhood and adulthood,['secondary ILD in childhood and adulthood'],,,264944,CN202346,,,,,,,,
mondo:0017036,Langerhans cell histiocytosis in childhood and adulthood,"['histiocytosis X in childhood and adulthood', 'Langerhans cell granulomatosis in childhood and adulthood']",,,264955,,,,,,,,,
mondo:0017039,drug or radiation exposure-related interstitial lung disease,,,,264978,CN202350,,,,,,,,
mondo:0017040,exposure-related interstitial lung disease,,,,264984,CN202351,,,,,,,,
mondo:0017041,osteochondrodysplatic nanism-deafness-retinitis pigmentosa syndrome,['Osteochondrodysplatic dwarfism-deafness-retinitis pigmentosa syndrome'],,,2653,CN202358,,,,,,,,
mondo:0017042,thanatophoric dysplasia,"['thanatophoric dwarfism', 'dwarfism thanatophoric', 'Td']",13481,,2655,C0039743,"['0.2576', '0.2258', '0.5713', '-0.041', '0.1284', '-0.2325', '0.3994', '0.8164', '-0.4104', '-0.668', '-0.4062', '-0.1277', '0.4998', '0.1824', '-0.292', '-0.383', '-0.00905', '-0.6587', '0.1299', '-0.726', '-0.1099', '-0.4854', '1.247', '0.2375', '-0.3223', '-0.264', '-0.665', '0.03412', '0.391', '-0.3196', '0.9077', '-0.2433', '-0.2267', '-0.1779', '-0.503', '-0.2622', '-0.1403', '-0.3696', '0.05823', '-0.374', '-0.13', '-0.3381', '0.4548', '0.04303', '-0.03293', '0.1322', '-0.2173', '0.2012', '-0.1925', '-0.396', '0.4094', '-0.1472', '-0.2798', '-0.4436', '-0.1807', '-0.359', '-0.04556', '0.1644', '0.4148', '0.665', '0.03427', '0.09076', '-0.428', '0.05682', '-0.2678', '0.331', '0.1549', '-0.6226', '-0.526', '0.3477', '0.0832', '0.1416', '0.6064', '-0.5317', '-0.5996', '-0.1431', '0.393', '-0.504', '-0.796', '-1.186', '-0.4685', '0.4536', '-0.3232', '0.5776', '-0.6973', '0.6753', '0.2754', '0.639', '0.734', '0.1987', '-0.5537', '-0.4617', '0.08887', '0.0887', '0.1111', '0.528', '0.8325', '-0.4785', '0.776', '0.2712']",C85187,,D013796,259.4,,10049808,
mondo:0017043,congenital mesoblastic nephroma,"['CMn', 'mesoblastic nephroma', 'stromal nephroma, malignant', 'congenital mesoblastic nephroma']",4773,,2665,C1332965,,C6569,,,,,10070665,
mondo:0017044,adult familial nephronophthisis-spastic quadriparesia syndrome,,,,2666,CN202376,,,,,,,,
mondo:0017045,neuroectodermal-endocrine syndrome,"['neuroectodermal endocrine syndrome', 'Oerter-Friedman-Anderson syndrome']",,,2676,CN202391,,,,,,,,
mondo:0017046,neuroepithelioma,,,,2677,,,,,,,,,
mondo:0017047,infantile axonal neuropathy,,,,2679,,,,,,,,,
mondo:0017048,pseudomyxoma peritonei,"['pseudomyxoma peritonei', 'gelatinous ascites', 'Myxoma peritonei', 'peritoneal cavity pseudomyxoma peritonei', 'Adenomucinosis', 'pseudomyxoma peritonei (morphologic abnormality)', 'PMP', 'mucinous ascites', 'well differentiated peritoneal mucinous adenocarcinoma', 'syndrome of pseudomyxoma peritonei']",3559,,26790,C0033822,,C3345,0007456,D011553,,,10037138,
mondo:0017049,hypomyelination neuropathy-arthrogryposis syndrome,['Boylan-dew syndrome'],,,2680,CN202399,,,,,,,,
mondo:0017050,intraocular medulloepithelioma,"['intraocular medulloepithelioma', 'orbital medulloepithelioma']",,,268139,CN202409,,C66806,,,,,,
mondo:0017051,classic maple syrup urine disease,"['classic branched-chain alpha-ketoacid dehydrogenase deficiency', 'classic BCKD deficiency', 'classic MSUD', 'classic branched-chain ketoaciduria', 'classic branched-chain 2-ketoacid dehydrogenase deficiency']",,,268145,,"['0.1781', '0.5146', '-0.2878', '0.07837', '-0.5825', '-1.212', '-0.4907', '0.4553', '-0.2493', '-0.3901', '-0.7544', '-0.4326', '0.477', '0.03726', '-0.04813', '-0.3765', '0.05847', '-0.7827', '0.3691', '-0.9614', '-0.4421', '-0.8125', '1.073', '0.113', '-0.314', '-0.5825', '-0.527', '-0.2742', '-0.2812', '-0.4001', '0.03087', '0.3655', '0.6523', '0.1934', '-0.4292', '0.8755', '0.1597', '0.3245', '-0.2421', '0.0718', '0.4736', '-0.1847', '0.298', '-0.1667', '-0.1287', '-0.1289', '-0.372', '-0.01382', '-0.1533', '1.24', '-0.5073', '-0.09564', '0.2258', '-0.9805', '0.3225', '-0.871', '0.4644', '-0.1267', '-0.316', '0.1333', '0.1179', '0.5615', '0.0874', '-0.1306', '-0.3618', '-0.0672', '0.3972', '-0.599', '-0.875', '0.1525', '-0.000573', '0.04126', '0.1333', '-0.3193', '-0.18', '0.2505', '0.3296', '-0.253', '-0.6104', '0.1334', '-0.02882', '-0.2327', '-0.4482', '-0.1175', '0.3613', '0.3196', '-0.11035', '-0.621', '0.03473', '0.514', '0.3958', '0.6816', '0.388', '0.1761', '0.19', '0.716', '-0.03116', '-0.5537', '0.07513', '0.01984']",,,,,,,
mondo:0017052,intermediate maple syrup urine disease,"['Intermediate MSUD', 'Intermediate BCKD deficiency', 'Intermediate branched-chain 2-ketoacid dehydrogenase deficiency', 'Intermediate branched-chain alpha-ketoacid dehydrogenase deficiency']",,,268162,,"['0.00856', '0.602', '-0.2454', '0.0718', '-0.129', '-1.052', '-0.743', '0.718', '-0.2522', '-0.00377', '-0.5386', '-0.3704', '0.5312', '0.305', '0.552', '-0.4849', '-0.1119', '-0.4744', '0.3572', '-0.917', '-0.0797', '-0.576', '0.721', '-0.4119', '-0.1785', '-0.3687', '-0.3916', '-0.3154', '0.1412', '-0.561', '0.1279', '0.2576', '0.983', '0.2319', '-0.2056', '0.785', '0.06775', '0.502', '-0.4863', '-0.114', '0.6436', '-0.2766', '-0.1545', '-0.1282', '0.11127', '-0.19', '0.051', '0.4023', '0.132', '0.838', '0.1305', '-0.4163', '-0.06525', '-0.6685', '0.2825', '-0.10754', '0.518', '0.01005', '-0.3582', '0.621', '-0.0776', '0.3584', '-0.00888', '-0.2913', '0.147', '-0.3171', '0.1569', '-0.3098', '-0.3816', '0.1664', '-0.176', '-0.04117', '-0.2384', '-0.2173', '0.07025', '0.2961', '-0.05222', '-0.3604', '-0.2954', '-0.2869', '0.4006', '-0.3843', '-0.3828', '0.08246', '0.6387', '0.2837', '-0.3352', '-0.8594', '0.3523', '0.61', '0.4773', '0.563', '0.2393', '0.1523', '-0.1644', '0.837', '-0.0601', '-0.5684', '-0.1168', '0.429']",,,,,,,
mondo:0017053,intermittent maple syrup urine disease,"['intermittent MSUD', 'intermittent branched-chain 2-ketoacid dehydrogenase deficiency', 'intermittent BCKD deficiency', 'intermittent branched-chain alpha-ketoacid dehydrogenase deficiency']",,,268173,,"['0.04395', '0.5063', '-0.277', '-0.1599', '-0.61', '-0.653', '-0.6157', '0.4084', '0.006012', '-0.1815', '-0.7676', '-0.277', '0.333', '0.2988', '-0.0512', '0.2', '-0.1664', '-0.402', '-0.1799', '-0.7266', '-0.2935', '-0.3245', '0.97', '-0.254', '-0.4097', '-0.4973', '-0.3623', '0.02635', '-0.0722', '-0.2522', '0.1866', '0.2247', '1.021', '0.3218', '-0.523', '0.4111', '-0.3777', '0.1786', '0.04297', '-0.04727', '0.6504', '-0.274', '0.2842', '-0.3196', '-0.0901', '-0.2996', '0.2588', '0.1093', '0.4429', '0.7407', '0.0686', '-0.0458', '0.2185', '-0.8013', '0.6104', '0.06396', '0.548', '-0.4578', '-0.6304', '0.3574', '-0.2185', '0.195', '0.261', '-0.0628', '-0.05304', '0.2988', '-0.131', '-0.1826', '-0.2583', '0.7363', '-0.521', '0.349', '-0.4412', '-0.4216', '0.0567', '0.2307', '-0.2612', '-0.2203', '-0.3064', '-0.0675', '0.10803', '-0.1345', '-0.4822', '-0.1067', '0.2236', '0.542', '-0.10736', '-1.023', '0.299', '0.6157', '0.4211', '0.3904', '-0.521', '-0.01223', '-0.3591', '1.056', '0.1141', '-0.3728', '-0.3342', '0.3386']",,,,,,,
mondo:0017054,thiamine-responsive maple syrup urine disease,"['thiamine-responsive branched-chain alpha-ketoacid dehydrogenase deficiency', 'thiamine-responsive branched-chain 2-ketoacid dehydrogenase deficiency', 'thiamine-responsive MSUD', 'thiamine-responsive BCKD deficiency']",,,268184,,"['-0.1104', '0.3472', '-0.1725', '-0.1322', '-0.5645', '-0.9004', '-0.6733', '0.4075', '0.05615', '-0.1492', '-0.2903', '-0.7036', '-0.04437', '0.3052', '0.374', '-0.1882', '-0.2249', '-0.617', '0.33', '-1.111', '-0.2556', '-0.51', '0.9062', '-0.04794', '-0.2032', '0.09753', '-0.2793', '-0.1353', '-0.2893', '-0.501', '0.0549', '0.3452', '0.5723', '0.6567', '-0.524', '0.526', '-0.1693', '0.315', '-0.431', '0.0165', '0.4102', '-0.4714', '-0.1486', '-0.1614', '0.010086', '0.04852', '-0.0823', '0.05304', '-0.2893', '0.829', '0.216', '0.0098', '-0.1764', '-0.5107', '0.396', '-0.2395', '0.758', '-0.11255', '-0.1356', '0.4492', '-0.0188', '0.1649', '0.03099', '-0.2084', '0.1858', '0.02948', '0.2585', '-0.3645', '-0.5615', '0.4927', '-0.1653', '0.08026', '0.181', '-0.1613', '0.03857', '0.905', '-0.2827', '-0.10065', '-0.364', '-0.1602', '0.02008', '-0.3782', '-0.2416', '0.2676', '0.8706', '0.0366', '-0.3315', '-0.594', '0.5645', '0.829', '0.4373', '0.304', '0.2263', '0.1685', '0.0755', '0.921', '-0.277', '-0.577', '0.2883', '0.1599']",,,,,,,
mondo:0017055,mycophenolate mofetil embryopathy,['MMF embryopathy'],,,268249,C4509879,,,,,,,,
mondo:0017056,DYRK1A-related intellectual disability syndrome due to 21q22.13q22.2 microdeletion,"['monosomy 21q22.13q22.2', 'Del(21)(q22.13q22.2)', '21q22.13q22.2 microdeletion syndrome', '21q22.13-q22.2 microdeletion syndrome', 'monosomy 21q22.13-q22.2']",,,268261,CN202414,,,,,,,,
mondo:0017057,hereditary thrombocytopenia with normal platelets,,,,268322,CN227073,"['-0.4072', '-0.1582', '-0.0511', '-0.1881', '0.0267', '0.01936', '-0.10675', '0.315', '0.1337', '-0.05792', '0.1448', '0.0499', '-0.01214', '-0.1957', '-0.03464', '-0.04376', '-0.06354', '-0.01779', '-0.06055', '-0.518', '-0.05978', '-0.00882', '0.4817', '-0.3872', '0.157', '-0.1005', '-0.134', '0.155', '0.2157', '-0.0936', '0.238', '-0.11224', '0.3647', '0.2551', '-0.05276', '-0.3916', '-0.6655', '-0.3337', '-0.11066', '-0.1334', '0.256', '0.06464', '0.01444', '-0.3784', '-0.1203', '-0.1569', '-0.252', '-0.1797', '0.05334', '-0.03934', '0.01259', '0.11194', '0.2487', '0.1757', '-0.13', '0.09625', '0.1351', '-0.3066', '-0.3035', '-0.006413', '-0.02292', '0.0837', '-0.009964', '-0.2585', '0.10455', '-0.0434', '0.2103', '0.31', '-0.33', '0.631', '-0.238', '0.05435', '-0.2961', '-0.1743', '0.3735', '-0.1121', '0.4841', '-0.07666', '0.403', '-0.1641', '-0.2607', '-0.2157', '0.1888', '0.219', '-0.09125', '0.3086', '-0.002485', '0.4316', '0.2047', '-0.2343', '0.1254', '0.4492', '0.1162', '-0.04102', '0.513', '0.5444', '0.1498', '-0.4028', '-0.004585', '0.1788']",,,,,,,
mondo:0017058,autosomal recessive intermediate Charcot-Marie-Tooth disease,"['intermediate Charcot-Marie-Tooth disease, autosomal recessive', 'RI-CMT']",,,268337,CN202416,"['0.1652', '0.4995', '0.08765', '0.2261', '-0.06506', '-0.1304', '-0.3235', '0.3386', '-0.728', '-0.005585', '-0.07306', '0.06476', '-0.2932', '0.2634', '-0.0662', '-0.349', '-0.09344', '-0.4048', '-0.3774', '-0.893', '-0.0829', '0.01727', '0.2747', '0.663', '0.2378', '0.606', '0.1866', '0.2493', '0.1907', '-0.0743', '-0.09973', '-0.8745', '0.2316', '0.4302', '0.2937', '-0.9', '-0.3474', '-0.1005', '0.4653', '-0.5835', '-1.756', '-0.1255', '-0.269', '0.5015', '-0.293', '-0.483', '0.225', '0.0658', '-0.02635', '0.0722', '0.177', '0.2384', '-0.3474', '-0.653', '0.568', '-0.033', '-0.05023', '0.521', '-0.7437', '-0.08136', '-0.4915', '0.02612', '1.038', '1.052', '-1.004', '1.185', '-0.04095', '0.655', '-0.698', '0.338', '-0.737', '0.1296', '0.305', '-0.461', '1.1455', '0.5107', '-0.4243', '0.5024', '0.3657', '-0.416', '-0.04578', '0.02724', '0.528', '0.581', '-0.02788', '-0.278', '0.03632', '0.433', '0.5703', '0.4524', '-0.0786', '-0.3281', '0.3586', '0.659', '0.5', '0.8687', '0.4207', '-0.6133', '-0.4712', '0.4583']",,,,,,,
mondo:0017059,neural tube closure defect,"['neural tube closure disease', 'disorder of neural tube closure']",,,268357,,"['-0.295', '0.0602', '0.1356', '-0.01775', '0.2861', '-0.187', '-0.06064', '0.2179', '-0.2175', '0.02953', '-0.1536', '-0.1487', '0.1384', '0.0568', '-0.155', '-0.1484', '-0.0647', '-0.21', '-0.1549', '-0.2854', '0.10266', '-0.03445', '0.1317', '-0.06714', '-0.00911', '-0.09', '0.0988', '0.0448', '0.0531', '-0.03032', '0.276', '0.0937', '0.2344', '0.11975', '0.06854', '-0.01203', '0.152', '-0.08466', '-0.01944', '-0.3384', '0.2615', '-0.1414', '0.1366', '-0.010666', '-0.204', '-0.1881', '0.089', '-0.05334', '0.01142', '0.12476', '-0.11487', '-0.1421', '0.024', '0.12134', '-0.1315', '-0.1509', '0.1436', '0.1301', '-0.1243', '-0.007267', '0.2048', '0.03293', '0.10254', '0.1342', '0.1105', '0.1952', '0.2612', '0.0695', '-0.2358', '0.1938', '-0.1425', '0.004814', '-0.03302', '-0.141', '-0.02328', '0.0735', '-0.01063', '-0.0496', '-0.0909', '-0.1263', '0.00345', '0.1442', '-0.0897', '0.2023', '-0.1277', '-0.04083', '0.10474', '0.1074', '0.2324', '-0.05908', '-0.0387', '0.2112', '-0.04965', '0.0887', '0.3118', '-0.1371', '0.0976', '-0.3142', '0.05563', '-0.002584']",,,,,,,
mondo:0017060,open iniencephaly,,,,268363,,,,,,,,,
mondo:0017061,closed iniencephaly,,,,268366,,,,,,,,,
mondo:0017062,spina bifida aperta,,,,268369,CN202421,,,,,,,,
mondo:0017063,total spina bifida aperta,,,,268377,CN202422,,,,,,,,
mondo:0017064,thoracolumbosacral spina bifida aperta,,,,268384,CN202423,,,,,,,,
mondo:0017065,lumbosacral spina bifida aperta,,,,268388,CN202424,,,,,,,,
mondo:0017066,cervical spina bifida aperta,,,,268392,CN202425,,,,,741.91,,,
mondo:0017067,cervicothoracic spina bifida aperta,,,,268397,CN202426,,,,,,,,
mondo:0017068,upper thoracic spina bifida aperta,,,,268740,CN202428,,,,,,,,
mondo:0017069,spina bifida cystica,"['meningomyelocele', 'open spina bifida', 'myelomeningocele', 'spina bifida, open', 'spina bifida manifesta', 'spina bifida aperta']",,,268744,,,C101201,,D016137,,,10071011,
mondo:0017070,total spina bifida cystica,,,,268748,,,,,,,,,
mondo:0017071,thoracolumbosacral spina bifida cystica,,,,268752,,,,,,,,,
mondo:0017072,lumbosacral spina bifida cystica,,,,268758,,,,,,,,,
mondo:0017073,cervical spina bifida cystica,,,,268762,,,,,,,,,
mondo:0017074,cervicothoracic spina bifida cystica,,,,268766,,,,,,,,,
mondo:0017075,upper thoracic spina bifida cystica,,,,268770,,,,,,,,,
mondo:0017076,posterior meningocele,,,,268810,CN202439,,,,,,,,
mondo:0017077,myelocystocele,,,,268813,,,,,,,,,
mondo:0017078,cephalocele,"['cephalocele (disease)', 'cranium bifidum', 'encephalocele', 'cephalocele']",,,268817,,,C84687,,,742.0,,,0011815
mondo:0017079,meningoencephalocele,"['cranial meningocele', 'encephalomeningocele', 'brain meninx cephalocele (disease)']",,,268820,C0009694,,C124517,,,,Q01.2,,
mondo:0017080,occipital encephalocele,,,,268823,,,,,,,Q01.2,,
mondo:0017081,parietal encephalocele,,,,268826,,,,,,,,,
mondo:0017082,basal encephalocele,,,,268829,C4023176,,,,,,,,
mondo:0017084,leptomyelolipoma,,,,268838,,,,,,,,,
mondo:0017086,primary tethered cord syndrome,"['occult spinal dysraphism', 'primary tethered spinal cord syndrome', 'segmental vertebral anomalies', 'tethered cord syndrome', 'occult spinal dysraphism sequence']",,,268861,CN202446,,,,,,,,
mondo:0017087,neurenteric cyst,,,,268865,,,,,,,,,
mondo:0017088,isolated amyelia,,,,268868,,,,,,,,,
mondo:0017089,isolated megalencephaly,"['isolated macrencephaly', 'nonsyndromic megalencephaly (disease)']",,,268920,,,,,,,,,
mondo:0017090,midline cerebral malformation,['Midline brain malformation'],,,268926,,,,,,,,,
mondo:0017091,bilateral polymicrogyria,,,,268940,,"['-0.08716', '-0.1115', '0.2864', '-0.1274', '0.03772', '0.04083', '0.2673', '-0.2197', '-0.1255', '-0.2477', '-0.4976', '-0.6445', '-0.1145', '0.0935', '0.1805', '-0.0754', '-0.1582', '-0.343', '-0.2051', '-0.937', '0.1583', '0.11127', '0.7666', '-0.1404', '0.4316', '0.22', '-0.3728', '0.12213', '-0.07605', '-0.0838', '0.3809', '-0.2018', '0.6406', '0.3271', '0.2754', '0.4941', '-0.564', '0.03958', '-0.1243', '-0.1971', '0.12146', '0.02979', '-0.014275', '-0.11694', '-0.0705', '-0.4856', '0.0336', '0.1849', '-0.091', '0.1192', '-0.0889', '0.1616', '-0.0671', '0.08997', '0.0002716', '0.206', '0.38', '-0.2925', '-0.2378', '0.523', '-0.04117', '0.03925', '0.3906', '0.1417', '0.05307', '-0.1455', '0.2942', '0.1597', '-0.3428', '0.678', '-0.3992', '0.3677', '0.0761', '0.1454', '-0.3164', '0.07776', '0.699', '0.2483', '-0.4443', '-0.2379', '-0.372', '0.02763', '-0.223', '0.4434', '0.2013', '-0.554', '0.05923', '0.401', '0.2686', '0.288', '0.1664', '0.35', '-0.03818', '0.1665', '0.0789', '0.2734', '0.6646', '-0.1827', '0.782', '-0.0887']",,,,,,,
mondo:0017092,unilateral polymicrogyria,,,,268943,C4024960,,,,,,,,
mondo:0017093,unilateral focal polymicrogyria,,0080919,,268947,,,,,,,,,
mondo:0017094,cerebral cortical dysplasia,"['cortical dysplasia', 'brain cortical dysplasia']",,,268950,,,C42088,,D054220,,,,
mondo:0017095,isolated focal cortical dysplasia type I,['FCD type I'],,,268961,CN202452,,,,,,,,
mondo:0017096,isolated focal cortical dysplasia type Ia,['FCD type Ia'],,,268973,CN202453,,,,,,,,
mondo:0017097,isolated focal cortical dysplasia type Ib,['FCD type IB'],,,268980,CN202454,,,,,,,,
mondo:0017098,isolated focal cortical dysplasia type Ic,['FCD type Ic'],,,268987,CN202455,,,,,,,,
mondo:0017100,neutropenia-monocytopenia-deafness syndrome,,,,2690,CN202458,,,,,,,,
mondo:0017101,isolated focal cortical dysplasia type IIa,['FCD type IIa'],,,269001,,"['-0.03348', '0.168', '0.0785', '-0.06042', '0.05255', '-0.07056', '0.04156', '0.0979', '-0.0873', '-0.02654', '-0.1317', '-0.0711', '-0.03113', '-0.02466', '-0.02069', '-0.01307', '0.04004', '-0.12384', '-0.000644', '-0.2825', '-0.0539', '0.01723', '0.2273', '-0.01724', '0.053', '-0.04495', '-0.02434', '-0.0693', '0.03278', '-0.02095', '0.094', '-0.0314', '0.1571', '0.03726', '0.07214', '-0.06058', '-0.04413', '-0.11304', '-0.01645', '-0.1862', '0.02263', '-0.1749', '0.02275', '-0.01782', '-0.05875', '-0.1101', '-0.06305', '0.1459', '0.05502', '-0.00692', '0.1042', '0.00979', '0.0685', '0.01912', '-0.11725', '-0.08777', '0.12274', '-0.07996', '-0.1527', '0.03072', '0.0789', '-0.001026', '-0.01113', '-0.09607', '-0.0699', '0.0573', '0.1958', '0.0636', '-0.1549', '0.10986', '-0.0848', '-0.014915', '0.10223', '-0.0975', '0.04492', '0.0666', '0.02177', '-0.00887', '-0.142', '-0.1082', '-0.02393', '0.1328', '-0.00889', '0.07336', '0.00526', '-0.0668', '-0.00254', '0.1901', '0.1791', '0.05084', '0.008736', '0.1282', '0.03497', '0.02698', '0.2844', '0.02548', '0.179', '-0.197', '0.0593', '0.10236']",,,,,,,
mondo:0017102,isolated focal cortical dysplasia type IIb,['FCD type IIb'],,,269008,CN202460,"['-0.01955', '0.1329', '0.0548', '-0.0578', '0.04745', '-0.063', '0.03128', '0.1228', '-0.0978', '-0.05826', '-0.1206', '-0.0858', '-0.0018835', '-0.005234', '-0.02658', '0.001744', '0.0399', '-0.1328', '-0.0342', '-0.2676', '-0.05096', '0.0001489', '0.2009', '0.000683', '0.02095', '-0.04214', '-0.04593', '-0.04266', '0.01625', '-0.02168', '0.0977', '-0.02512', '0.1515', '0.02934', '0.05173', '-0.0466', '-0.03394', '-0.0958', '-0.01227', '-0.1725', '0.0511', '-0.1514', '0.01782', '-0.03503', '-0.02533', '-0.10474', '-0.0785', '0.0989', '0.0259', '0.002178', '0.094', '0.00846', '0.04736', '0.00967', '-0.10956', '-0.07623', '0.1165', '-0.0704', '-0.1334', '0.04297', '0.0751', '0.001215', '-0.00507', '-0.0706', '-0.0814', '0.0767', '0.2002', '0.0714', '-0.1388', '0.1108', '-0.0897', '0.004677', '0.0919', '-0.10675', '0.0656', '0.04865', '0.03473', '0.003525', '-0.12146', '-0.0856', '-0.04117', '0.148', '-0.013466', '0.1014', '0.012314', '-0.03165', '0.02228', '0.1821', '0.1816', '0.067', '0.03056', '0.1375', '0.03384', '0.02728', '0.2705', '0.0572', '0.1565', '-0.1692', '0.0457', '0.10175']",,,,,,,
mondo:0017103,encephaloclastic disorder,,,,269190,CN227080,,,,,,,,
mondo:0017104,central nervous system cystic malformation,,,,269194,,,,,,,,,
mondo:0017105,glioependymal/ependymal cyst,,,,269197,,,,,,,,,
mondo:0017106,retrocerebellar cyst,"['Retrocerebellar arachnoid cyst', 'retrocerebellar cyst (disease)', 'Retrocerebellar cyst']",,,269200,,,,,,,,,0006951
mondo:0017107,isolated cerebellar vermis agenesis,,,,269203,,,,,,,,,
mondo:0017108,isolated total cerebellar vermis agenesis,,,,269206,,,,,,,,,
mondo:0017109,isolated partial cerebellar vermis agenesis,,,,269209,,,,,,,,,
mondo:0017110,isolated Dandy-Walker malformation with hydrocephalus,,,,269212,,,,,,,,,
mondo:0017111,isolated Dandy-Walker malformation without hydrocephalus,,,,269215,,,,,,,,,
mondo:0017112,isolated unilateral hemispheric cerebellar hypoplasia,,,,269218,,,,,,,,,
mondo:0017113,isolated bilateral hemispheric cerebellar hypoplasia,,,,269221,,,,,,,,,
mondo:0017114,global cerebellar malformation,['diffuse cerebellar malformation'],,,269224,,,,,,,,,
mondo:0017116,congenital communicating hydrocephalus,['congenital non-obstructive hydrocephalus'],,,269505,,"['-0.1794', '-0.03568', '0.0374', '0.4922', '-0.2783', '-0.4246', '-0.05655', '0.5728', '-0.531', '0.6504', '-0.02693', '-0.773', '-0.4316', '0.54', '0.2451', '-0.1608', '-0.574', '0.3308', '-0.9604', '-1.201', '-0.1073', '-0.3523', '0.262', '-0.3572', '-0.3064', '-0.7227', '-0.8926', '0.904', '-0.3525', '0.6587', '-0.4026', '-1.082', '0.4565', '-0.2722', '-0.4116', '0.502', '-0.1943', '0.09674', '0.1199', '-0.656', '0.921', '0.527', '0.2186', '-0.5396', '0.806', '-0.00609', '0.7075', '-0.628', '0.414', '0.44', '0.2103', '0.04132', '-0.1702', '-0.691', '0.3079', '-0.3105', '0.10187', '0.276', '0.1209', '0.0898', '-0.564', '0.6143', '-0.502', '0.02814', '-0.06244', '0.4949', '0.1018', '0.04022', '-1.102', '0.0326', '-0.1703', '1.125', '0.01566', '-0.9966', '0.2079', '0.4456', '0.385', '0.9624', '-0.31', '-0.8804', '-0.2864', '-0.3997', '-0.6064', '0.51', '0.3289', '0.7373', '0.6436', '0.00251', '0.493', '-0.1859', '-0.1816', '0.8335', '0.1345', '0.2979', '0.59', '0.5127', '0.3154', '-0.4353', '-0.2445', '0.09796']",,,,,,,
mondo:0017117,congenital non-communicating hydrocephalus,['congenital obstructive hydrocephalus'],,,269510,,,,,,,,,
mondo:0017123,arthrogryposis-renal dysfunction-cholestasis syndrome,"['arthrogryposis-renal dysfunction-cholestasis', 'arthrogryposis, renal dysfunction and cholestasis (ARC) syndrome', 'arthrogryposis multiplex congenita, renal dysfunction, and cholestasis', 'ARC syndrome', 'arthrogryposis, renal dysfunction, and cholestasis', 'arthrogryposis renal dysfunction cholestasis syndrome', 'arthrogryposis - renal dysfunction - cholestasis']",0050763,,2697,,"['-0.354', '0.879', '-0.04437', '0.253', '-0.3928', '-0.742', '0.2084', '0.6694', '-0.2224', '-0.4595', '-0.1427', '-0.6587', '0.2837', '-0.06885', '-0.7715', '0.3098', '0.721', '0.0523', '-0.0836', '-0.6587', '0.2644', '-0.0513', '0.503', '0.576', '-0.00999', '-0.1829', '-0.1627', '0.5786', '0.1864', '-0.02348', '0.1134', '0.05603', '0.1882', '0.0806', '0.11426', '-0.6626', '-1.308', '-0.2214', '-0.2329', '0.42', '-0.01102', '-0.658', '0.07965', '-0.3157', '-0.256', '-0.2418', '0.3687', '-0.0804', '0.03348', '-0.3843', '-0.1807', '0.5454', '-0.2913', '-0.0495', '-0.1399', '-0.829', '0.4302', '-0.3347', '-0.00962', '0.695', '0.3596', '0.06', '0.1062', '-0.753', '-0.01804', '-0.02226', '0.387', '0.5356', '-0.7104', '0.2993', '-0.5615', '0.2678', '-0.1415', '0.3245', '0.03072', '-0.1316', '0.5195', '-0.6323', '-0.1727', '0.4963', '0.4458', '0.481', '-0.2062', '-0.05035', '-0.3145', '0.4521', '-0.06116', '0.09515', '0.05173', '-0.582', '0.6694', '0.4023', '-0.385', '-0.1752', '0.672', '0.358', '0.02818', '-0.7793', '0.1215', '0.613']",,,C535382,,,,
mondo:0017124,noma,"['oro-facial noma', 'noma neonatorum', 'cancrum oris', 'oro-facial gangrene', 'gangrenous stomatitis', 'oral gangrene']",9672,,2700,C0028271,,C34852,1001063,D009625,528.1,,10029502,
mondo:0017126,oculo-skeletal-renal syndrome,['oculo skeletal renal syndrome'],,,2716,CN202523,,,,,,,,
mondo:0017127,inherited soft tissue tumor,"['genetic mesenchymal cell neoplasm', 'genetic soft tissue tumor', 'genetic mesenchymal tumour', 'genetic mesenchymal tumor', 'hereditary mesenchymal cell neoplasm', 'genetic soft tissue tumour']",,,271832,CN202526,,,,,,,,
mondo:0017128,inherited digestive tract tumor,"['genetic digestive tract tumour', 'genetic digestive tract tumor']",,,271835,CN202527,,,,,,,,
mondo:0017129,inherited cardiac tumor,"['genetic heart tumor', 'hereditary heart neoplasm', 'genetic heart tumour', 'genetic cardiac tumour', 'genetic cardiac tumor']",,,271841,CN202528,,,,,,,,
mondo:0017131,hereditary cardiac anomaly,['genetic cardiac anomaly'],,,271853,,"['-0.065', '0.03708', '0.01663', '-0.006638', '0.04056', '-0.09235', '0.0473', '0.1497', '-0.0796', '-0.05185', '-0.00818', '-0.01556', '0.02342', '0.0402', '-0.07697', '-0.0355', '-0.04712', '-0.0442', '-0.0821', '-0.1997', '0.01738', '0.00985', '0.09906', '-0.0139', '0.04565', '-0.00973', '-0.03017', '-0.001285', '0.05856', '-0.0449', '0.1062', '0.00634', '0.13', '0.06866', '0.006344', '-0.0566', '0.00495', '-0.03436', '-0.005314', '-0.1349', '0.03482', '-0.07776', '0.07056', '-0.06067', '-0.00734', '-0.106', '-0.01608', '0.08356', '0.02095', '0.03995', '-0.03308', '-0.0374', '0.02724', '-0.03442', '-0.0707', '-0.0505', '0.0628', '-0.003172', '-0.1152', '-0.02771', '0.086', '0.02127', '0.02075', '-0.01405', '0.001052', '0.01926', '0.09595', '0.0748', '-0.1084', '0.1244', '-0.1009', '0.02078', '0.02058', '-0.04846', '0.04752', '0.03473', '0.02896', '-0.027', '-0.09106', '-0.0455', '-0.02109', '-0.001365', '0.01137', '0.11774', '-0.0409', '-0.01634', '0.06476', '0.0831', '0.10846', '0.0331', '0.05298', '0.1066', '-0.005234', '0.03674', '0.2112', '0.0365', '0.1279', '-0.1465', '-0.03745', '0.0695']",,,,,,,
mondo:0017132,hereditary ATTR amyloidosis,"['familial transthyretin-related amyloidosis', 'familial TTR-related amyloidosis']",,,271861,CN227096,"['0.4648', '-0.6626', '-0.5645', '0.381', '0.2512', '-0.375', '-0.5835', '0.4739', '-1.428', '0.05963', '-0.0791', '0.1205', '-1.222', '0.4138', '-0.8706', '-0.01402', '-0.002138', '-0.00793', '-0.04514', '-0.822', '0.3987', '-0.2314', '0.4758', '-0.177', '0.02722', '0.4055', '-0.501', '-0.1103', '0.4924', '0.36', '0.1571', '-0.5767', '0.804', '-0.783', '0.555', '-0.7656', '-0.339', '0.2703', '0.4534', '-0.1182', '0.0862', '-0.06866', '-0.1638', '0.4045', '0.4126', '-0.6885', '-0.4485', '0.384', '0.527', '0.934', '0.014046', '0.702', '0.32', '-0.2043', '-0.5107', '-0.11975', '0.509', '0.159', '-0.477', '-1.018', '-0.3728', '0.4333', '0.6475', '-0.825', '0.1382', '-0.262', '0.3748', '0.972', '-0.854', '0.3926', '-0.364', '0.3718', '-0.6235', '-0.4026', '0.4568', '0.663', '-0.5093', '1.356', '-0.4707', '-0.8555', '-0.421', '-0.4019', '-0.0936', '-0.1655', '0.3293', '-0.392', '-0.2446', '-0.1083', '0.1426', '-0.0975', '0.4246', '-0.468', '-0.4277', '-0.08295', '0.663', '0.558', '-0.7524', '-0.4634', '0.003258', '-0.0187']",,,,,,,
mondo:0017134,odonto-onycho dysplasia-alopecia syndrome,['odonto onycho dysplasia with alopecia'],,,2722,CN202534,,,,,,,,
mondo:0017135,olivopontocerebellar atrophy-deafness syndrome,['olivopontocerebellar atrophy deafness'],,,2732,CN202542,,,,,,,,
mondo:0017136,omodysplasia,,0060288,,2733,C4510897,"['-0.1191', '0.0621', '-0.06097', '-0.4736', '0.2468', '-0.1652', '0.1373', '0.8115', '-0.928', '-0.483', '0.01223', '-0.0646', '0.1324', '0.3691', '-0.1743', '0.277', '0.556', '0.04218', '-0.652', '-0.714', '-0.4656', '0.2866', '0.705', '-0.04276', '0.04382', '0.1456', '-0.0392', '-0.596', '0.4138', '-0.1173', '0.0217', '-0.0384', '-0.1304', '-0.0406', '0.3372', '-0.05453', '-0.3357', '-0.4016', '0.003426', '0.1254', '0.05734', '-0.7363', '0.03317', '0.1343', '0.2537', '-0.2437', '-0.1284', '0.1702', '-0.0739', '-0.3647', '0.1122', '-0.4626', '-0.09375', '0.1387', '-0.3245', '-1.038', '0.1393', '-0.03485', '0.0618', '-0.10455', '-0.11896', '-0.2402', '-0.02249', '0.4404', '-0.04407', '-0.2876', '-0.0682', '0.1948', '-0.368', '0.1199', '-0.3567', '0.2112', '0.167', '-0.385', '-0.2288', '0.638', '-0.053', '-0.07214', '-0.408', '0.04895', '0.10895', '0.2334', '0.86', '0.8467', '0.04614', '0.689', '0.1138', '0.2795', '0.007507', '0.1746', '-0.2128', '0.0636', '0.4102', '0.1998', '1.067', '0.0781', '0.8564', '-0.7427', '0.1716', '0.05273']",,,,,,,
mondo:0017137,onchocerciasis,"['Robles^ disease', 'volvulosis', 'River blindness', 'Onchocerca volvulus infection']",11678,,2737,C0029001,,C34861,0007402,D009855,125.3,B73,10039202,
mondo:0017138,Opitz G/BBB syndrome,"['hypertelorism-oesophageal abnormality-hypospadias syndrome', 'hypospadias-hypertelorism syndrome', 'hypospadias-dysphagia, syndrome', 'Opitz-Frias syndrome', 'Opitz syndrome', 'hypospadias-dysphagia syndrome', 'G syndrome', 'hypertelorism with esophageal abnormality and hypospadias', 'Opitz BBBG syndrome', 'hypertelorism hypospadias syndrome', 'BBB syndrome', 'Opitz-GBBB syndrome', 'GBBB syndrome', 'Opitz G/BBB syndrome', 'Opitz GBBB syndrome', 'telecanthus with associated abnormalities', 'Opitz-G syndrome, type 2', 'Opitz G syndrome']",0080697,,2745,CN202554,"['0.3508', '0.5044', '-0.2917', '-0.267', '0.2761', '-0.3376', '0.2113', '0.3855', '-1.079', '-0.92', '-0.2527', '-0.7153', '-0.05295', '0.2466', '-0.224', '0.10144', '-0.3982', '-0.2847', '-0.12134', '-0.4504', '0.1137', '0.567', '0.564', '-0.4187', '-0.2073', '-0.32', '-0.4048', '0.1063', '1.157', '-0.528', '0.6245', '0.005257', '0.231', '-0.205', '0.3955', '-0.2864', '-0.5444', '-0.0782', '-0.738', '-0.3704', '0.07043', '-0.57', '0.578', '-0.3628', '0.619', '-0.4197', '-0.6895', '0.2869', '-0.5166', '0.5376', '-0.2837', '-0.273', '-0.658', '-0.31', '-0.1332', '-0.4097', '0.3354', '0.5786', '-0.256', '0.621', '-0.204', '-0.04147', '0.4546', '1.038', '0.323', '0.11334', '-0.2208', '0.1062', '-0.856', '0.3677', '-0.001583', '0.3154', '-0.208', '0.4006', '0.295', '0.2391', '0.575', '-0.3718', '-0.7666', '-0.00716', '0.1381', '-0.2664', '-0.002274', '0.5557', '0.439', '0.6157', '-0.171', '0.1764', '-0.0817', '0.1311', '-0.11444', '0.05624', '0.2651', '0.09204', '1.259', '-0.4875', '0.0639', '-0.1288', '0.4395', '0.00673']",C125487,,,758.89,,,
mondo:0017139,oromandibular-limb hypogenesis syndrome,"['Oroacral syndrome', 'oro-mandibular-limb hypogenesis syndrome']",,,2749,CN202556,,,,,,,,
mondo:0017140,L1 syndrome,"['corpus callosum hypoplasia-retardation-adducted thumbs-spasticity-hydrocephalus syndrome', 'CRASH syndrome', 'L1CAM syndrome']",,,275543,CN118845,"['0.2283', '0.2517', '0.1168', '-0.283', '-0.3198', '-0.4514', '-0.0731', '0.3237', '-0.8813', '-0.754', '-0.194', '-0.3489', '0.1765', '0.07764', '0.724', '-0.1471', '-0.524', '-0.2289', '0.175', '-0.8174', '0.07965', '0.2764', '1.031', '-0.1353', '-0.0852', '-0.4158', '-0.1365', '0.421', '0.4417', '-0.02608', '0.5234', '-0.5337', '0.862', '0.237', '-0.283', '-0.2273', '-0.4077', '-0.6177', '0.296', '0.1132', '-0.08405', '-0.3816', '0.3801', '-0.1299', '0.4854', '-0.387', '-0.3655', '-0.0273', '0.2013', '-0.1893', '-0.504', '0.4827', '-0.5527', '-0.7427', '-0.4202', '0.3818', '-0.2163', '0.0238', '-0.1512', '0.772', '-0.6685', '-0.141', '0.3892', '0.549', '-0.3303', '0.3137', '-0.193', '0.6763', '-0.64', '0.1807', '-0.0796', '0.3018', '0.03708', '-0.3782', '0.2067', '0.2266', '0.2812', '0.0889', '-0.1571', '-0.4578', '-0.2751', '-0.3567', '-0.2289', '0.6953', '0.37', '0.491', '0.03195', '0.0903', '-0.2622', '-0.308', '0.1434', '0.1647', '-0.183', '0.0885', '0.605', '-0.61', '0.3215', '-0.352', '0.4077', '0.4692']",,,,,,,
mondo:0017144,alpha-thalassemia and related diseases,,,,275745,CN202570,,,,,,,,
mondo:0017145,beta-thalassemia and related diseases,,,,275749,CN202571,,,,,,,,
mondo:0017146,sickle cell disease and related diseases,,,,275752,CN202572,,,,,,,,
mondo:0017147,idiopathic pulmonary arterial hypertension,"['primary pulmonary arterial hypertension', 'IPAH']",,,275766,CN202574,,,,,416.0,,10065151,
mondo:0017148,heritable pulmonary arterial hypertension,"['familial pulmonary arterial hypertension', 'FPAH', 'HpaH', 'hereditary pulmonary arterial hypertension']",,,275777,CN202575,,C121945,,,,,,
mondo:0017149,drug- or toxin-induced pulmonary arterial hypertension,['drug- or toxin-induced PAH'],,,275786,C0340544,,,0009192,,,,,
mondo:0017157,pulmonary hypertension owing to lung disease and/or hypoxia,"['pulmonary hypertension due to lung disease and/or hypoxia', 'PH due to lung disease and/or hypoxia', 'PH owing to lung disease and/or hypoxia']",,,275837,CN202580,,,,,416.8,,,
mondo:0017160,behavioral variant of frontotemporal dementia,['bv-FTD'],,,275864,C4011788,"['0.3525', '-0.05185', '-0.1669', '-0.3545', '-0.5034', '-0.319', '0.1053', '0.2012', '-1.043', '-0.4607', '-0.0807', '-0.486', '-0.02571', '0.7217', '0.3235', '-0.8657', '-0.328', '-0.3962', '-0.4602', '0.1412', '0.2208', '-0.206', '-0.1687', '-0.03635', '0.9116', '-0.3303', '-0.2266', '0.11743', '-0.1715', '-0.1959', '0.12195', '-0.1383', '-0.0601', '-0.5396', '0.7153', '-0.3145', '-0.457', '-0.3052', '0.492', '-1.177', '0.7236', '-0.6074', '0.255', '-0.0983', '0.0596', '-0.2229', '0.544', '-0.4775', '0.4421', '0.3066', '0.1388', '0.176', '0.3198', '-0.544', '0.1348', '0.368', '-0.00669', '-0.4717', '-0.4753', '-0.682', '-0.108', '0.3198', '0.4756', '-0.8203', '0.11285', '0.711', '0.2764', '0.968', '-0.8735', '0.766', '0.3796', '-0.058', '0.133', '-0.1349', '-0.2983', '0.975', '0.1522', '0.309', '-0.934', '0.0188', '-0.314', '-0.732', '-0.379', '1.049', '0.6', '0.5874', '-0.105', '-0.11163', '1.448', '0.7754', '0.2627', '0.635', '-0.1559', '0.6865', '-0.551', '0.392', '-0.4558', '-0.09625', '-0.4712', '-0.4915']",,,,,,,
mondo:0017161,frontotemporal dementia with motor neuron disease,"['FTD-ALS', 'frontotemporal dementia with amyotrophic lateral sclerosis', 'frontotemporal dementia with ALS', 'FTD-MND', 'FTDALS']",,,275872,CN239493,"['0.3215', '-0.01122', '-0.2404', '-0.5146', '-0.4197', '-0.239', '0.1022', '0.1807', '-1.043', '-0.503', '-0.05432', '-0.2462', '0.1863', '0.761', '0.4817', '-0.921', '-0.4404', '-0.3867', '-0.4285', '0.1582', '0.306', '-0.307', '-0.197', '0.03014', '0.885', '-0.3425', '-0.2986', '0.00853', '-0.2693', '-0.0993', '0.2363', '-0.1272', '-0.076', '-0.4958', '0.8745', '-0.4294', '-0.5566', '-0.3098', '0.3884', '-1.23', '0.707', '-0.617', '0.2252', '-0.127', '0.0428', '-0.0636', '0.642', '-0.4465', '0.5557', '0.3013', '0.311', '0.1649', '0.275', '-0.562', '0.191', '0.2128', '0.03586', '-0.3975', '-0.534', '-0.4949', '-0.1106', '0.3623', '0.4216', '-0.9585', '0.1804', '0.834', '0.2944', '1.019', '-0.722', '0.6626', '0.3271', '-0.1676', '0.1044', '-0.067', '-0.4304', '0.94', '0.1604', '0.2698', '-0.928', '0.04376', '-0.2148', '-0.8013', '-0.3086', '1.01', '0.6753', '0.64', '0.007343', '-0.1641', '1.561', '0.7993', '0.2437', '0.579', '-0.2164', '0.676', '-0.487', '0.448', '-0.449', '0.05182', '-0.3894', '-0.4482']",,,C566288,,,,
mondo:0017162,imperforate oropharynx-costo vetebral anomalies syndrome,"['imperforate oropharynx-costo vetebral anomalies', 'imperforate oropharynx-costovertebral anomalies syndrome', 'Seghers syndrome']",,,2759,CN202584,,,,,,,,
mondo:0017164,hemolytic disease of the newborn with Kell alloimmunization,"['maternal anti-Kell alloimmunization', 'anti-K HDN']",,,275944,CN202586,,,,,,,,
mondo:0017165,bile acid CoA ligase deficiency and defective amidation,,,,276066,C4274079,,,,,,,,
mondo:0017167,malignant epithelial tumor of salivary glands,"['malignant epithelial tumor of the salivary glands', 'malignant epithelial tumour of the salivary glands']",,,276145,CN202591,,,,,,,,
mondo:0017168,benign epithelial tumor of salivary glands,,,,276148,CN202592,,,,,,D11.0,,
mondo:0017169,multiple endocrine neoplasia,"['multiple endocrine neoplasia syndrome(s)', 'multiple endocrine neoplasia', 'men syndrome', 'multiple endocrine neoplasia syndrome', 'multiple endocrine adenomatosis', 'men syndromes', 'men']",3125,,276161,C0027662,,C6432,,D009377,258.0,,10061299,
mondo:0017170,idiopathic recurrent stupor,,,,276174,CN202595,,,,,,,,
mondo:0017171,"mucopolysaccharidosis type 6, rapidly progressing","['mucopolysaccharidosis type VI, rapidly progressing', 'MPSVI, rapidly progressing', 'MPS6, rapidly progressing', 'arylsulfatase B deficiency, rapidly progressing']",,,276212,CN202600,,,,,,,,
mondo:0017172,"mucopolysaccharidosis type 6, slowly progressing","['mucopolysaccharidosis type VI, slowly progressing', 'MPSVI, slowly progressing', 'MPS6, slowly progressing', 'arylsulfatase B deficiency, slowly progressing']",,,276223,CN202601,,,,,,,,
mondo:0017173,non-syndromic male infertility due to sperm motility disorder,"['nonsyndromic male infertility due to sperm motility disorder', 'isolated male infertility due to sperm motility disorder', 'non-syndromic male infertility due asthenozoospermia']",,,276234,CN202602,"['-0.4265', '-0.6177', '0.2216', '-0.5835', '-0.1224', '-0.3215', '-0.0947', '0.5054', '-0.3792', '-0.3118', '1.638', '-0.12024', '-0.1431', '1.126', '-0.0633', '-0.2164', '0.04153', '0.576', '-0.6787', '-1.369', '-0.303', '0.133', '0.1993', '-0.438', '0.2805', '-0.8765', '0.1804', '0.03427', '-0.7764', '-0.5503', '0.4314', '0.0792', '-0.3237', '-0.11334', '0.0612', '0.08466', '-0.1112', '-0.163', '0.1395', '0.01477', '0.2205', '0.3127', '0.1617', '-0.249', '0.747', '-0.6626', '0.2178', '-0.695', '0.7397', '0.4985', '-0.7134', '-0.2534', '-0.03717', '0.5044', '-0.1067', '0.608', '0.1879', '0.2025', '-0.737', '0.417', '0.277', '0.853', '-0.1537', '0.1792', '-0.2773', '0.4543', '-0.06192', '0.6196', '-1.129', '0.5557', '-0.3123', '0.2385', '0.003313', '-0.2983', '0.1874', '0.7695', '0.618', '0.5137', '-0.2405', '0.3486', '-0.0221', '0.3623', '0.11237', '-0.7173', '-0.202', '-0.568', '0.1648', '0.0236', '0.2886', '-0.741', '-0.5767', '0.4258', '-0.766', '1.194', '0.638', '-0.394', '0.2659', '-0.3264', '-0.71', '0.1482']",,,,,,,
mondo:0017174,Machado-Joseph disease type 1,"['spinocerebellar ataxia type 3, Joseph type', 'SCA3, Joseph type']",,,276238,,,,,,,,,
mondo:0017175,Machado-Joseph disease type 2,"['spinocerebellar ataxia, Thomas type', 'SCA3, Thomas type']",,,276241,,,,,,,,,
mondo:0017176,Machado-Joseph disease type 3,"['spinocerebellar ataxia type 3, Machado type', 'SCA3, Machado type']",,,276244,,,,,,,,,
mondo:0017177,hemihyperplasia-multiple lipomatosis syndrome,['HHML'],,,276280,CN202613,,,,,,,,
mondo:0017178,osteochondritis dissecans,"['König disease', 'osteochondritis dissecans', 'osteochondritis dissecans (disease)', 'osteochondritis dissecans and short stature', 'osteochondritis dissecans, short stature, and early-onset osteoarthritis', 'Koenig disease', 'OCD', 'SSOAOD', 'short stature and advanced bone Age, with or without early-onset osteoarthritis and/Or osteochondritis Dissecans', 'OD', 'Konig disease', 'familial osteochondritis dissecans']",84,,2764,C0029421,"['0.096', '0.0755', '-0.7925', '-0.0867', '-0.302', '-0.4543', '0.3123', '0.711', '-1.078', '0.06046', '0.5654', '0.5596', '0.1193', '0.8804', '0.476', '0.2205', '-0.093', '0.0604', '-0.1296', '-0.3108', '0.02261', '0.1302', '0.1714', '0.02345', '-0.4001', '0.12396', '-0.1459', '0.1131', '0.275', '0.1006', '-0.298', '-0.4504', '0.4312', '0.06223', '0.1266', '0.2102', '-0.1484', '0.0603', '0.2964', '-1.219', '0.564', '-0.5073', '-0.3867', '0.09326', '0.438', '0.0936', '-0.2542', '-0.1473', '0.584', '0.3132', '-0.1929', '-0.1863', '0.4949', '0.5317', '0.1292', '-0.3074', '-0.2832', '-0.265', '-0.1653', '-0.3884', '0.58', '0.1898', '-0.2477', '-0.4646', '-0.00911', '0.188', '0.5415', '0.5093', '-0.1454', '-0.11237', '-0.2737', '0.05325', '-0.613', '-0.7515', '0.3384', '0.1251', '0.0291', '1.075', '0.4722', '-0.5845', '-0.1919', '-0.368', '0.2869', '0.3826', '-0.169', '0.07196', '-0.303', '-0.0925', '0.2754', '-0.3774', '-0.366', '0.1694', '-0.9834', '0.588', '0.2817', '0.4429', '0.729', '-0.5444', '-0.2786', '-0.4504']",C34878,,D010008,732.7,,10031231,0010886
mondo:0017179,limbic encephalitis with caspr2 antibodies,,,,276402,,,,,,,,,
mondo:0017180,10q22.3q23.3 microduplication syndrome,"['dup(10)(q22.3q23.3)', 'trisomy 10q22.3q23.3']",,,276422,CN202619,,,,,,,,
mondo:0017181,hypnic headache,"['hypnic headache', 'hypnic headache (disease)']",,,276429,,,,,D051270,339.81,,,0012459
mondo:0017182,familial hyperinsulinism,"['HHI', 'hereditary hyperinsulinism (disease)', 'nesidioblastosis', 'hyperinsulinemic hypoglycemia', 'familial hyperinsulinemic hypoglycemia', 'congenital hyperinsulinism', 'FHI', 'neonatal hyperinsulinism', 'hyperinsulinemia of infancy']",,,276525,,"['-0.001335', '0.2751', '-0.0384', '0.093', '0.0817', '-0.3462', '0.0008163', '-0.1985', '0.0789', '-0.0908', '-0.01119', '-0.2627', '0.1971', '-0.0932', '-0.252', '-0.096', '-0.12256', '-0.1691', '0.06137', '-0.4546', '0.2397', '-0.1373', '0.269', '-0.0977', '0.1608', '0.006413', '0.2068', '-0.1824', '0.1149', '-0.15', '0.5186', '0.2094', '0.1934', '0.10223', '-0.2179', '-0.0666', '-0.0699', '0.1967', '-0.3267', '-0.1265', '0.1731', '-0.3162', '0.2289', '0.009', '0.10297', '-0.0894', '-0.09875', '0.0245', '0.3198', '0.3628', '-0.1305', '-0.2615', '0.005096', '0.02498', '-0.0743', '-0.2025', '0.266', '0.1164', '-0.304', '0.2253', '0.06494', '0.05698', '0.2861', '-0.2976', '-0.303', '-0.04044', '0.294', '0.1086', '-0.2695', '0.2913', '-0.2927', '-3.86e-05', '0.227', '-0.12146', '-0.01723', '0.3025', '0.01421', '0.1573', '-0.4353', '-0.2089', '0.1293', '0.1449', '-0.3477', '-0.1975', '-0.07336', '0.1749', '0.2083', '0.1405', '0.3909', '0.0679', '0.07104', '0.1891', '0.1938', '-0.1411', '0.2969', '0.1597', '0.1262', '-0.277', '-0.3625', '-0.03111']",C131425,,,,,,
mondo:0017183,hyperinsulinism due to UCP2 deficiency,['hyperinsulinemic hypoglycemia due to UCP2 deficiency'],,,276556,C4303082,,,,,,,,
mondo:0017184,autosomal dominant hyperinsulinism due to SUR1 deficiency,['autosomal dominant hyperinsulinemic hypoglycemia due to SUR1 deficiency'],,,276575,CN202625,,,,,,,,
mondo:0017185,autosomal dominant hyperinsulinism due to Kir6.2 deficiency,"['dominant KATP hyperinsulinism due to Kir6.2 deficiency', 'autosomal dominant hyperinsulinemic hypoglycemia due to Kir6.2 deficiency']",,,276580,CN202626,"['-0.4592', '0.5244', '-0.0752', '0.1255', '-0.3665', '-0.589', '0.06696', '-0.08716', '0.1162', '-0.3428', '-0.10583', '0.4453', '0.04926', '0.1445', '-0.1335', '-0.0638', '-0.2161', '-0.2615', '0.133', '-0.782', '-0.399', '-0.2216', '0.5225', '0.11395', '-0.352', '0.4148', '-0.4878', '-0.1052', '-0.2019', '-0.743', '-0.137', '0.403', '0.0136', '0.00217', '-0.7373', '-0.2913', '-0.107', '0.2598', '-0.1337', '-0.2383', '0.3494', '-0.5615', '0.09674', '-0.2524', '-0.5684', '-0.03616', '-0.2122', '0.1351', '0.2947', '0.3376', '0.9336', '-0.1453', '-0.1724', '0.2903', '-0.1836', '-0.482', '0.563', '-0.1324', '-0.4575', '0.807', '-0.0878', '0.28', '0.556', '0.0775', '-0.0559', '0.1942', '0.4546', '0.5576', '0.09296', '0.4812', '-0.28', '0.05652', '0.8325', '-0.328', '0.5635', '0.5894', '-0.201', '-0.1758', '0.06134', '-0.1163', '-0.2225', '0.482', '-0.06964', '0.11346', '0.06555', '0.898', '0.1425', '-0.134', '1.001', '0.512', '0.4875', '0.515', '-0.327', '0.003672', '0.139', '0.371', '0.2998', '-0.604', '-0.02724', '0.1444']",,,,,,,
mondo:0017186,diazoxide-resistant hyperinsulinism,['diazoxide-resistant hyperinsulinemic hypoglycemia'],,,276585,,,,,,,,,
mondo:0017187,diazoxide-resistant focal hyperinsulinism due to SUR1 deficiency,"['hyperinsulinemic hypoglycemia due to SUR1 deficiency, diazoxide-resistant focal form']",,,276598,,"['-0.208', '0.5005', '-0.0889', '0.0589', '-0.1917', '-0.0759', '0.0512', '0.1034', '0.1947', '0.05087', '-0.4363', '-0.0799', '0.2795', '-0.0799', '-0.3782', '-0.1382', '-0.0803', '-0.02809', '-0.1552', '-0.672', '0.04712', '0.01439', '0.3813', '-0.12036', '-0.07965', '-0.1148', '0.1932', '-0.05435', '-0.0368', '-0.05725', '0.199', '0.2146', '0.2461', '0.3718', '-0.5225', '-0.09576', '-0.04794', '0.01564', '-0.3657', '0.0382', '-0.1388', '-0.246', '0.2373', '0.006325', '-0.2461', '-0.1106', '-0.0633', '-0.1065', '0.1278', '0.4238', '-0.107', '-0.0971', '0.1755', '0.05258', '0.02347', '0.09076', '0.4185', '-0.2983', '-0.2205', '0.2527', '-0.000562', '0.1692', '-0.11975', '-0.4187', '0.07684', '0.04724', '0.3513', '0.348', '-0.6294', '0.12177', '-0.007214', '0.3447', '0.1305', '-0.3665', '0.11926', '-0.2595', '0.3818', '-0.05597', '-0.15', '0.0967', '-0.1515', '0.1175', '-0.1482', '-0.03836', '0.3013', '0.518', '-0.132', '0.0869', '0.7515', '0.0787', '0.3638', '0.3787', '-0.227', '-0.2118', '0.2903', '0.2039', '0.1866', '-0.3577', '0.05054', '0.3857']",,,,,,,
mondo:0017188,diazoxide-resistant focal hyperinsulinism due to Kir6.2 deficiency,"['hyperinsulinemic hypoglycemia due to Kir6.2 deficiency, diazoxide-resistant focal form']",,,276603,,"['-0.2178', '0.515', '-0.07025', '0.06116', '-0.2272', '-0.11676', '0.05408', '0.0901', '0.1835', '0.0149', '-0.4604', '-0.0201', '0.226', '-0.1372', '-0.3655', '-0.1406', '-0.0809', '-0.0454', '-0.10986', '-0.7227', '0.03287', '0.02301', '0.425', '-0.0985', '-0.0803', '-0.1071', '0.1528', '-0.0602', '-0.07697', '-0.09326', '0.1917', '0.2527', '0.186', '0.3381', '-0.556', '-0.02745', '-0.03363', '0.0587', '-0.3347', '-0.0082', '-0.1455', '-0.2474', '0.2773', '-0.01846', '-0.2766', '-0.1153', '-0.1565', '-0.0722', '0.1021', '0.422', '-0.08374', '-0.08716', '0.1481', '-0.02614', '0.02574', '0.0769', '0.4465', '-0.291', '-0.1793', '0.2646', '0.01619', '0.1492', '-0.07947', '-0.4175', '0.1161', '0.0657', '0.3767', '0.329', '-0.594', '0.164', '0.01888', '0.3582', '0.1602', '-0.358', '0.1797', '-0.2568', '0.36', '-0.0752', '-0.1511', '0.03806', '-0.1681', '0.1287', '-0.09344', '-0.0497', '0.3025', '0.4822', '-0.1354', '0.0808', '0.7764', '0.0882', '0.3616', '0.4104', '-0.2047', '-0.1985', '0.2825', '0.1626', '0.2094', '-0.3918', '0.03168', '0.3992']",,,,,,,
mondo:0017189,adult-onset non-insulinoma persistent hyperinsulinemic hypoglycemia,['NI-PHH'],,,276608,C4274082,,,,,,,,
mondo:0017190,sporadic pheochromocytoma/secreting paraganglioma,,,,276621,CN202630,,,,,,,,
mondo:0017191,sporadic pheochromocytoma,,,,276624,CN202631,,,,,,,,
mondo:0017192,sporadic secreting paraganglioma,,,,276627,CN202632,,,,,,,,
mondo:0017193,symptomatic form of Coffin-Lowry syndrome in female carriers,,,,276630,CN202633,,,,,,,,
mondo:0017194,Blount disease,"['Osteochondrosis deformans tibiae', 'Blount disease', 'familial infantile type osteochondrosis deformans tibiae', 'Blount^s disease', 'tibia vara', 'Osteochondrosis deformans tibiae, familial infantile type', 'infantile tibia vara', 'tibia vara Blount', 'Blount-Barber syndrome', 'Erlacher-Blount syndrome']",14798,,2768,,,C118460,,C536237,736.89,,10072255,
mondo:0017195,Bruck syndrome,"['osteogenesis imperfecta with congenital joint contractures', 'osteogenesis imperfecta-congenital joint contractures syndrome']",0060231,,2771,C0432253,"['-0.3406', '0.02951', '0.322', '-0.2378', '0.399', '-0.4324', '0.02477', '0.8223', '-0.3965', '-0.31', '-0.1917', '0.1224', '-0.3281', '-0.064', '0.10693', '0.274', '0.563', '0.1965', '-0.2386', '-0.3699', '0.1117', '0.08636', '0.2197', '-0.2815', '0.03046', '0.2593', '-0.1122', '-0.196', '0.1262', '-0.04742', '0.012474', '-0.3733', '0.156', '0.3442', '0.08417', '-0.3774', '0.08746', '-0.5337', '-0.03232', '-0.04227', '-0.0777', '-0.2942', '-0.1004', '-0.04172', '-0.0371', '-0.2847', '0.02277', '0.4258', '-0.0544', '-0.3713', '0.04752', '-0.1021', '0.2311', '0.1321', '-0.323', '-0.2803', '0.005547', '-0.31', '-0.1534', '0.005524', '0.3306', '0.03198', '-0.3176', '-0.1746', '-0.1283', '-0.1691', '0.09515', '0.611', '-0.37', '0.2966', '-0.3604', '0.03687', '0.03943', '-0.395', '0.1411', '0.2585', '-0.2578', '0.1539', '-0.11566', '-0.1809', '0.11316', '0.1947', '0.0442', '0.4329', '-0.4597', '0.3293', '0.1318', '0.43', '0.10126', '-0.1193', '0.158', '0.1786', '-0.1376', '-0.0012455', '0.379', '0.1249', '0.6226', '-0.5024', '0.1255', '0.0356']",,,,733.99,,10063718,
mondo:0017196,osteogenesis imperfecta-retinopathy-seizures-intellectual disability syndrome,"['Al Gazali-Nair syndrome', 'Al Gazali Sabrinathan Nair syndrome', 'osteogenesis imperfecta retinopathy seizures intellectual deficit']",,,2773,CN202641,,,,C535617,,,,
mondo:0017197,osteopathia striata-pigmentary dermopathy-white forelock syndrome,"['Whyte Murphy syndrome', 'Whyte-Murphy syndrome', 'osteopathia striata with pigmentary dermopathy including white forelock', 'osteopathia striata associated with familial dermopathy and white forelock']",,,2779,C2931096,,,,C536054,,,,
mondo:0017198,osteopetrosis,"['Albers-Schonberg disease', 'osteopetrosis (disease)', 'osteosclerosis fragilis', 'marble bones', 'osteopetrosis', 'osteopetroses', 'marble bone disease', 'marble bone', 'osteopetrosis and related disorders', 'Albers-Schoenberg disease']",13533,,2781,,,C26840,,D010022,756.52,,10031280,0011002
mondo:0017199,osteoporosis-macrocephaly-blindness-joint hyperlaxity syndrome,['Heide syndrome'],,,2787,CN202651,,,,,,,,
mondo:0017200,polycystic ovaries-urethral sphincter dysfunction syndrome,"['fowler-Christmas-Chapple syndrome', 'voiding dysfunction and polycystic ovaries', 'fowler Christmas Chapple syndrome', 'polycystic ovaries urethral sphincter dysfunction', 'fowler^s syndrome']",,,2795,C2931462,,,,C537271,,,,
mondo:0017201,Spasmus nutans,"['Spasmus nutans', 'Spasmus nutans (disease)']",,,279882,C1527306,,,,,,,10059593,0010533
mondo:0017202,acute endophthalmitis,"['endophthalmitis, acute']",11752,,279888,C0154773,,,,,360.01,,10000730,
mondo:0017203,chronic endophthalmitis,"['endophthalmitis, chronic']",10697,,279891,C0154774,,,,,360.03,,10008864,
mondo:0017204,toxic maculopathy due to antimalarial drugs,,,,279894,CN202676,,,,,,H35.3,,
mondo:0017205,primary oculocerebral lymphoma,['primary oculocerebral non-Hodgkin lymphoma'],,,279897,,,,,,,,,
mondo:0017207,primary organ-specific lymphoma,,,,279911,C1334465,,C7185,,,,,,
mondo:0017209,infectious posterior uveitis,,,,279919,,,,,,,,,
mondo:0017210,infectious anterior uveitis,"['secondary infected iridocyclitis', 'secondary iridocyclitis, infectious', 'infectious secondary iridocyclitis']",9389,,279922,C0154911,,,,,364.03,,,
mondo:0017211,infectious panuveitis,,,,279925,,,,,,,,,
mondo:0017212,paraneoplastic uveitis,,,,279928,,,,,,,,,
mondo:0017213,postorgasmic illness syndrome,"['POIS', 'post orgasmic sick syndrome']",,,279947,CN202682,,,,,,,,
mondo:0017214,vitamin B12-responsive methylmalonic acidemia,"['adenosylcobalamin deficiency', 'vitamin B12-responsive methylmalonic aciduria']",,,28,,,,,,,,,
mondo:0017215,calciphylaxis,['idiopathic calciphylaxis'],4734,,280062,C0006666,,C84607,,D002115,275.49,,10051714,
mondo:0017216,calciphylaxis cutis,,,,280065,C4274083,,,,,,,,
mondo:0017217,visceral calciphylaxis,,,,280068,,,,,,,,,
mondo:0017218,septopreoptic holoprosencephaly,['Septopreoptic HPE'],,,280195,CN202699,,,,,,,,
mondo:0017219,microform holoprosencephaly,"['HPE, minor form', 'HPE-L', 'HoloprosencC)phalie, minor form', 'holoprosencephaly-like', 'Microform HPE', 'Holoprosencéphalie, minor form']",0111380,,280200,CN236719,"['-0.1635', '0.3157', '0.3296', '-0.5205', '0.11273', '0.1268', '0.5225', '0.2185', '-0.7563', '-0.01373', '-0.543', '-0.1346', '0.2012', '0.2888', '-0.1375', '-0.525', '0.0962', '-0.479', '-0.2537', '-0.1323', '0.2064', '0.1572', '0.7666', '-0.1912', '0.547', '-0.2366', '0.07947', '0.09985', '0.4932', '0.0615', '0.1242', '0.06903', '0.4783', '0.1425', '0.1984', '-0.337', '-0.11273', '-0.3394', '-0.3245', '-0.5366', '0.3132', '-0.2449', '0.1334', '-0.2164', '0.05664', '-0.1015', '0.0635', '0.03033', '-0.4163', '0.4094', '0.04794', '0.1691', '-0.4092', '-0.1173', '-0.367', '-0.3975', '0.2343', '0.07733', '-0.04602', '0.4746', '-0.11786', '0.1315', '0.209', '0.2457', '-0.362', '-0.11444', '0.613', '0.3162', '-0.5596', '0.0776', '0.02524', '0.2952', '0.622', '-0.2546', '-0.5244', '-0.1021', '0.7563', '-0.1687', '-0.4998', '-0.2201', '-0.2255', '-0.0633', '0.03247', '0.4604', '-0.1478', '-0.3733', '0.00881', '0.4675', '0.134', '0.338', '0.0756', '0.8936', '0.4639', '0.1852', '0.866', '-0.3557', '0.463', '-0.4114', '0.595', '0.1279']",,,,,Q04.2,,
mondo:0017220,laryngotracheoesophageal cleft type 0,"['laryngo-tracheo-esophageal cleft type 0', 'LTEC0']",,,280205,CN202702,,,,,,,,
mondo:0017221,"Pelizaeus-Merzbacher disease, connatal form","['severe PMD', 'connatal PMD', 'Pelizaeus-Merzbacher disease type II']",,,280210,CN202703,,,,,,,,
mondo:0017222,"Pelizaeus-Merzbacher disease, classic form",['classic PMD'],,,280219,,,,,,,,,
mondo:0017223,"Pelizaeus-Merzbacher disease, transitional form",['transitional PMD'],,,280224,,,,,,,,,
mondo:0017224,Pelizaeus-Merzbacher disease in female carriers,,,,280229,CN202706,,,,,,,,
mondo:0017225,null syndrome,"['PLP1 null syndrome', 'Pelizaeus-Merzbacher disease, null syndrome']",,,280234,CN202707,,,,,,,,
mondo:0017226,Pelizaeus-Merzbacher-like disease,['PMLD'],,,280270,,"['-0.3557', '0.639', '0.03595', '-0.3928', '0.0845', '-0.7373', '-0.602', '0.2098', '-0.8403', '0.1074', '-0.385', '0.01479', '0.09393', '-0.3054', '0.8477', '0.06537', '0.2006', '-0.3516', '-0.05905', '-0.786', '0.311', '-0.3525', '0.2786', '-0.02864', '-0.03372', '0.2903', '-0.3223', '-0.06494', '0.1595', '-0.1636', '0.05936', '0.625', '0.2051', '-0.1892', '0.1046', '-0.12274', '-0.3147', '-0.575', '0.0326', '-0.4414', '0.2742', '-0.4355', '-0.0757', '0.4087', '0.0957', '-0.354', '0.0768', '0.442', '-0.2057', '-0.1565', '0.2318', '0.04404', '-0.881', '-0.4436', '-0.02357', '-0.3943', '0.5737', '0.111', '-0.6816', '0.1357', '0.03644', '0.3535', '0.1467', '0.2147', '0.462', '-0.1962', '0.3938', '0.2732', '0.02676', '0.2861', '-0.763', '-0.342', '0.197', '-0.297', '0.343', '-0.03452', '-0.10345', '-0.2001', '-0.1696', '-0.4883', '0.245', '-0.2344', '-0.004612', '0.6167', '-0.252', '0.203', '0.07166', '0.1317', '0.295', '0.2605', '0.3208', '0.5703', '0.05148', '0.4146', '0.5415', '0.762', '0.2717', '0.2546', '0.3625', '-0.1637']",,,,,,,
mondo:0017227,autoimmune pancreatitis type 1,"['autoimmune pancreatitis type 1', 'AIP type 1', 'lymphoplasmacytic sclerosing pancreatitis', 'IgG4-related pancreatitis']",,,280302,CN202712,,,1000780,,,,,
mondo:0017228,autoimmune pancreatitis type 2,"['duct-centric pancreatitis', 'AIP type 2']",,,280315,CN202713,,,,,,,,
mondo:0017229,distal monosomy 12p,"['12p13.33 microdeletion syndrome', 'distal monosomy type 12p', 'Del(12)(p13.33)', 'distal deletion 12p']",,,280325,CN202714,,,,,,,,
mondo:0017230,autosomal semi-dominant severe lipodystrophic laminopathy,,,,280365,CN202719,,,,,,,,
mondo:0017231,erythropoietic uroporphyria associated with myeloid malignancy,,,,280379,,,,,,,,,
mondo:0017232,recessive intellectual disability-motor dysfunction-multiple joint contractures syndrome,['IDMDC'],,,280384,,,,,,,,,
mondo:0017233,familial Alzheimer-like prion disease,,,,280397,CN202723,,,,,,,,
mondo:0017234,inherited prion disease,"['familial prion disease', 'hereditary prion disease']",,,280400,CN202725,,,,,,,,
mondo:0017235,familial omphalocele syndrome with facial dysmorphism,,,,280403,CN202726,,,,,,,,
mondo:0017236,rapidly progressive glomerulonephritis,"['RPGN', 'crescentic glomerulonephritis']",4776,,280569,C0221239,,C35264,,,583.4,,10018378,
mondo:0017237,hereditary sensorimotor neuropathy with hyperelastic skin,,,,280598,CN202738,,,,,,,,
mondo:0017238,hemoglobinopathy Toms River,"['transient neonatal cyanosis and anemia due to Toms River Hemoglobin', 'transient neonatal cyanosis and anaemia due to Toms River Haemoglobin']",,,280615,,"['-0.2942', '0.227', '0.01663', '0.01221', '0.1283', '-0.33', '-0.0487', '0.2542', '-0.1267', '-0.172', '-0.10974', '0.0873', '0.367', '-0.0883', '-0.2576', '-0.4065', '-0.11566', '0.10657', '-0.1792', '-0.55', '-0.1732', '-0.0871', '0.4358', '-0.04263', '0.3367', '0.0429', '0.3857', '0.11255', '0.1451', '0.0173', '0.0536', '0.2695', '0.3894', '0.1727', '-0.2632', '-0.01883', '-0.1365', '-0.02556', '-0.01278', '-0.2', '-0.0412', '0.044', '0.1631', '-0.0963', '-0.4062', '-0.1392', '-0.11304', '0.05762', '-0.000274', '-0.0864', '-0.04535', '-0.1421', '0.2644', '0.0754', '-0.04315', '-0.02335', '0.0361', '0.08765', '0.01022', '0.371', '0.1718', '0.0892', '0.07983', '-0.2637', '-0.153', '-0.2568', '0.4602', '0.244', '-0.4263', '0.1038', '0.1004', '-0.1019', '-0.0233', '-0.0495', '-0.03445', '-0.07306', '0.303', '-0.1154', '-0.0939', '0.001987', '0.003914', '-0.10596', '0.006126', '-0.11066', '0.010216', '-0.0695', '0.0892', '0.3513', '0.28', '-0.056', '0.368', '0.1447', '-0.03033', '-0.0876', '0.3015', '0.4404', '0.1179', '-0.353', '-0.07874', '0.168']",,,,,,,
mondo:0017239,familial progressive hyper- and hypopigmentation,['FPHH'],,,280628,,,,,,,,,
mondo:0017240,acrodysostosis with multiple hormone resistance,,,,280651,CN202748,"['-0.1284', '0.2063', '0.1095', '-0.04196', '0.0984', '-0.1742', '-0.011314', '0.1544', '-0.09595', '-0.1703', '-0.0179', '-0.03967', '0.0753', '-0.0326', '-0.004993', '-0.07007', '0.03256', '0.03604', '-0.0881', '-0.3254', '-0.00218', '-0.057', '0.08466', '-0.1229', '0.0627', '0.0739', '-0.09424', '-0.11145', '0.11523', '-0.1218', '0.1519', '0.03696', '0.1925', '0.08826', '0.014854', '-0.12134', '0.001424', '-0.06415', '-0.0977', '-0.2085', '0.0556', '-0.1526', '0.0769', '-0.1343', '0.02364', '-0.2156', '0.0433', '0.1858', '-0.0198', '0.01071', '-0.05966', '-0.02197', '0.03638', '0.1075', '-0.267', '0.01851', '0.1329', '-0.162', '-0.1682', '0.09015', '0.182', '0.04697', '-0.0521', '-0.04062', '-0.03668', '-0.06137', '0.1787', '0.0821', '-0.1864', '0.0849', '-0.1707', '0.01262', '0.04214', '-0.1158', '0.03354', '0.001626', '-0.03326', '-0.03387', '-0.1206', '-0.01643', '0.0202', '0.1968', '-0.1328', '0.1443', '-0.05923', '0.02036', '0.0642', '0.1635', '0.226', '0.0894', '0.1509', '0.1087', '-0.0332', '-0.0324', '0.3257', '0.01519', '0.1221', '-0.2369', '0.04398', '0.1131']",,,,,,,
mondo:0017241,AP4-related intellectual disability and spastic paraplegia,"['severe intellectual disability and progressive spastic paraplegia', 'AP4 deficiency syndrome', 'AP4 related intellectual disability and spastic paraplegia']",,,280763,CN202757,"['-0.268', '0.4197', '0.2101', '-0.364', '-0.2786', '-0.5884', '-0.11993', '0.5605', '-0.535', '-0.3892', '0.02606', '0.0384', '0.06866', '-0.0608', '0.522', '-0.2727', '0.12354', '0.005085', '-0.03784', '-0.613', '0.12463', '0.09094', '-0.00242', '-0.1384', '0.3188', '-0.02649', '-0.0327', '0.06235', '-0.07385', '-0.2476', '0.1659', '-0.003351', '0.524', '0.4434', '0.14', '-0.1577', '-0.0755', '-0.138', '-0.02052', '-0.0362', '0.1936', '-0.4187', '-0.309', '0.2502', '-0.2205', '-0.283', '-0.2888', '0.02457', '0.0481', '0.007217', '-0.2737', '0.2952', '-0.1538', '-0.05344', '0.2769', '-0.2314', '0.05804', '-0.009834', '-0.08655', '0.3584', '-0.0741', '0.03035', '0.3591', '0.2002', '-0.2228', '0.078', '0.161', '0.4646', '-0.3086', '0.2441', '-0.2412', '0.06323', '0.2356', '-0.2354', '0.0959', '-0.02068', '0.1636', '0.014824', '0.0002933', '0.1641', '0.03552', '0.1014', '-0.0767', '0.47', '0.1381', '0.2786', '-0.0158', '0.3374', '0.5996', '0.527', '0.2247', '0.3516', '0.05847', '0.1431', '0.4382', '0.1676', '0.2952', '-0.2708', '0.512', '0.12067']",,,,,,,
mondo:0017242,cutaneous collagenous vasculopathy,"['cutaneus colagenous vasculopathy', 'CCV']",,,280779,C4305323,,,,,,,,
mondo:0017243,bullous diffuse cutaneous mastocytosis,['bullous DCM'],,,280785,,,,,,,,,
mondo:0017244,pseudoxanthomatous diffuse cutaneous mastocytosis,"['Pseudoxanthomatous DCM', 'infiltrative small vesicular diffuse cutaneous mastocytosis', 'infiltrative small vesicular DCM']",,,280794,,,,,,,,,
mondo:0017245,intralobar congenital pulmonary sequestration,"['intralobar congenital bronchopulmonary sequestration', 'congenital intrapulmonary sequestration']",,,280802,,,,,,,,,
mondo:0017246,extralobar congenital pulmonary sequestration,"['extralobar congenital bronchopulmonary sequestration', 'congenital extrapulmonary sequestration']",,,280811,,,,,,,,,
mondo:0017247,communicating congenital bronchopulmonary-foregut malformation,,,,280821,,,,,,,,,
mondo:0017248,congenital pulmonary airway malformation type 0,"['congenital cystic adenomatous malformation of the lung type 0', 'congenital cystic adenomatoid malformation of the lung type 0', 'CPAM type 0']",,,280827,,,,,,,,,
mondo:0017249,congenital pulmonary airway malformation type 1,"['congenital cystic adenomatous malformation of the lung type 1', 'congenital cystic disease of the lung type 1', 'CPAM type 1', 'congenital cystic adenomatoid malformation of the lung type 1', 'CCAM type 1']",,,280832,,,,,,,,,
mondo:0017250,congenital pulmonary airway malformation type 2,"['CPAM type 2', 'congenital cystic disease of the lung type 2', 'CCAM type 2', 'congenital cystic adenomatoid malformation of the lung type 2', 'congenital cystic adenomatous malformation of the lung type 2']",,,280840,,,,,,,,,
mondo:0017251,congenital pulmonary airway malformation type 3,"['congenital cystic adenomatoid malformation of the lung type 3', 'CPAM type 3', 'CCAM type 3', 'congenital cystic disease of the lung type 3', 'congenital cystic adenomatous malformation of the lung type 3']",,,280847,,,,,,,,,
mondo:0017252,congenital pulmonary airway malformation type 4,"['congenital cystic adenomatous malformation of the lung type 4', 'congenital cystic adenomatoid malformation of the lung type 4', 'CPAM type 4']",,,280854,,,,,,,,,
mondo:0017255,panuveitis,"['panuveitis (disease)', 'total uveitis', 'diffuse uveitis', 'panuveitis']",12030,,280898,,,C84989,1001082,D015864,360.12,,10033687,0012121
mondo:0017256,idiopathic anterior uveitis,,,,280914,C0339315,,,,,,,,
mondo:0017257,idiopathic posterior uveitis,,,,280917,,,,,,,,,
mondo:0017258,idiopathic panuveitis,,,,280921,,,,,,,,,
mondo:0017262,inherited non-syndromic ichthyosis,['nonsyndromic inherited ichthyosis'],,,281082,,,,,,,,,
mondo:0017263,inherited ichthyosis syndromic form,"['syndromic inherited ichthyosis', 'syndrome associated with inherited ichthyosis']",,,281085,,,,,,,,,
mondo:0017264,syndromic recessive X-linked ichthyosis,"['syndromic X-linked ichthyosis', 'recessive X-linked ichthyosis with extracutaneous manifestations', 'syndromic RXLI', 'syndrome associated with recessive X-linked ichthyosis', 'syndromic recessive X-linked ichthyosis']",,,281090,CN202782,,,,,,,,
mondo:0017265,autosomal recessive congenital ichthyosis,"['ARCI', 'ichthyosis, congenital, autosomal recessive', 'inherited ichthyosis, autosomal recessive']",0060655,,281097,,"['-0.0791', '0.2052', '-0.00972', '-0.0709', '0.1963', '-0.275', '-0.09064', '0.0548', '-0.09', '-0.1615', '-0.0485', '0.02997', '-0.01166', '-0.0049', '-0.0378', '0.00614', '0.0453', '-0.1354', '-0.0673', '-0.3875', '-0.1799', '-0.04395', '0.1763', '-0.013435', '-0.00405', '0.10114', '-0.1142', '-0.1063', '0.1088', '-0.1989', '0.1306', '0.1167', '0.1119', '0.10925', '-0.0873', '-0.01726', '-0.01281', '-0.1909', '0.039', '-0.227', '0.03366', '-0.3289', '0.1109', '0.0854', '-0.03625', '-0.2607', '-0.1021', '0.1204', '0.1271', '0.0498', '0.0463', '-0.11145', '0.02245', '-0.1509', '-0.06274', '-0.1979', '0.2695', '0.1132', '-0.3083', '-0.0658', '0.1738', '-0.04843', '0.07935', '0.02202', '0.0933', '0.004826', '0.2312', '0.1257', '-0.2192', '0.1837', '-0.305', '-0.1388', '0.01936', '-0.1432', '0.1716', '0.1721', '0.006733', '-0.02664', '-0.04755', '-0.0959', '0.0281', '-0.01968', '-0.04175', '0.197', '0.01176', '0.09735', '0.07306', '0.1967', '0.0908', '0.1803', '0.1483', '0.2384', '0.0853', '0.126', '0.382', '0.1648', '0.2798', '-0.3252', '0.03207', '0.02481']",,,,,,,
mondo:0017266,keratinopathic ichthyosis,['KPI'],,,281103,C4511307,,,,,,,,
mondo:0017267,self-healing collodion baby,"['self-improving congenital ichthyosis', 'SHCB', 'SICI', 'self-improving collodion baby']",,,281122,C1855789,,,,C565473,,,,
mondo:0017268,acral self-healing collodion baby,['acral SHCB'],,,281127,,,,,,,,,
mondo:0017269,X-linked ichthyosis syndrome,"['inherited ichthyosis syndromic form, X-linked', 'X-linked inherited ichthyosis syndromic form']",,,281210,C0079588,,,,,,,10048063,
mondo:0017270,autosomal ichthyosis syndrome,,,,281217,CN202791,,,,,,,,
mondo:0017275,spastic paraplegia-facial-cutaneous lesions syndrome,"['Bahemuka-Brown syndrome', 'spastic paraplegia facial cutaneous lesions', 'Bahemuka Brown syndrome']",,,2819,C2931617,,,,C537797,,,,
mondo:0017276,frontotemporal dementia,"['frontotemporal lobe dementia (FLDEM)', 'MSTD', 'pallidopontonigral degeneration', 'FTD', 'Wilhemsen-Lynch disease', 'multiple system tauopathy with presenile dementia', 'frontotemporal lobar degeneration']",9255,,282,C0520716,"['0.3125', '-0.10254', '-0.2266', '-0.2566', '-0.3943', '-0.1461', '0.1234', '-0.00533', '-0.892', '-0.4197', '-0.10626', '-0.559', '0.2118', '0.5874', '0.4792', '-0.888', '-0.2783', '-0.3616', '-0.4563', '0.2465', '0.2102', '-0.1361', '-0.10284', '0.1107', '0.781', '-0.2374', '-0.1472', '0.1733', '-0.1226', '-0.1019', '0.2886', '-0.2822', '-0.0196', '-0.4465', '0.9404', '-0.4685', '-0.3457', '-0.5503', '0.2015', '-1.1875', '0.6357', '-0.657', '0.3154', '-0.01627', '0.1415', '-0.02129', '0.5894', '-0.4824', '0.2983', '0.3755', '0.1301', '0.1134', '0.324', '-0.5107', '0.0822', '0.2964', '0.016', '-0.6216', '-0.559', '-0.5596', '-0.1012', '0.228', '0.3098', '-0.9365', '-0.0295', '0.6025', '0.1692', '0.95', '-0.7744', '0.72', '0.2585', '0.0727', '0.0479', '0.00517', '-0.4849', '0.898', '-0.0731', '0.254', '-0.8286', '0.01955', '-0.03625', '-0.715', '-0.5303', '0.948', '0.6406', '0.586', '-0.1763', '-0.3262', '1.44', '0.687', '0.2412', '0.492', '-0.1768', '0.812', '-0.498', '0.4275', '-0.401', '-0.1449', '-0.4543', '-0.326']",C84719,,D057180,,,10068968,
mondo:0017277,partial deletion of chromosome 12,"['partial monosomy of chromosome 12', 'partial deletion of chromosome type 12']",,,282124,,,,,,,,,
mondo:0017278,autoimmune polyendocrinopathy,"['autoimmune polyendocrine syndrome; polyglandular autoimmune syndrome', 'autoimmune polyendocrine syndrome', 'autoimmune polyglandular syndrome(s)', 'autoimmune polyglandular failure', 'autoimmune polyendocrinopathy syndrome', 'autoimmune polyendocrinopathy', 'Lloyd^s syndrome', 'APS', 'autoimmune polyglandular syndrome']",14040,,282196,C4316913,,C84576,,,258.8,E31.0,,
mondo:0017279,young-onset Parkinson disease,"['early-onset Parkinson^s disease', 'YOPD', 'early-onset Parkinson disease']",0060894,,391411,,"['0.05463', '0.3489', '-0.5986', '-0.4453', '-0.6973', '-0.523', '0.3694', '0.8726', '-0.691', '0.2773', '-0.129', '0.591', '-0.3574', '-0.05063', '0.4834', '-0.0849', '0.2366', '-0.547', '-0.1455', '-0.561', '-0.1382', '-0.709', '0.3606', '-0.1703', '-0.04785', '0.2842', '0.3088', '-0.2435', '-0.3606', '-0.632', '0.666', '0.2656', '0.9175', '-0.58', '-0.01614', '-0.1409', '-0.2917', '-0.3262', '0.1509', '-0.02982', '0.2384', '-0.6353', '0.06232', '-0.3113', '0.9473', '-0.2489', '-0.2742', '-0.498', '-0.269', '0.9824', '0.61', '0.578', '-1.004', '-0.2024', '-0.1707', '0.4155', '0.646', '-0.728', '-0.2869', '0.1636', '0.6323', '0.4934', '0.278', '-0.6357', '-0.3', '0.4797', '0.1245', '0.0849', '0.295', '0.9434', '0.2937', '-0.5737', '-0.026', '-0.4734', '0.7725', '1.027', '0.1523', '0.0519', '-0.668', '-0.5806', '0.2386', '-0.1021', '0.6265', '0.919', '0.3438', '0.6104', '-0.2327', '-0.5117', '0.8555', '0.10956', '-0.1985', '-0.267', '-0.03433', '0.861', '0.6543', '0.6753', '0.724', '0.4797', '-0.2622', '-0.6733']",,,,,,,
mondo:0017280,demodicidosis,"['Demodicosis', 'demodectic mange', 'Demodex caused disease or disorder', 'red mange']",,,283,C3854478,,,,,,,,
mondo:0017281,renal caliceal diverticuli-deafness syndrome,,,,2838,CN202834,,,,,,,,
mondo:0017282,alveolar echinococcosis,"['echinococcus multilocularis infection', 'Echinococcus multilocularis caused disease or disorder', 'Echinococcus multilocularis infection', 'alveolococcosis', 'echinococcosis', 'small fox tapeworm', 'multilocular hydatid']",12148,,284,C0948954,,,,C536591,122.7,,10053042,
mondo:0017283,DeSanto-Shinawi Syndrome due to 10p11.21p12.31 microdeletion,"['monosomy 10p11.21p12.31', '10p12p11 microdeletion syndrome', 'deletion 10p11.21p12.31', 'facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to 10p11.21p12.31 microdeletion', 'Del(10)(p11.21p12.31)']",,,284169,CN202845,"['-0.1476', '0.1718', '0.6274', '-0.1864', '-0.01259', '-0.249', '0.213', '0.594', '-0.3313', '-0.04086', '-0.07495', '-0.1268', '0.3115', '-0.2627', '-0.04788', '0.04126', '0.1973', '-0.248', '-0.3247', '-0.4224', '-0.04422', '0.1656', '0.04544', '0.005833', '0.277', '-0.311', '-0.196', '-0.02086', '0.2908', '-0.2345', '0.12', '0.0535', '0.4116', '0.227', '0.0986', '-0.1669', '-0.12384', '-0.09735', '-0.1649', '-0.5825', '0.262', '-0.124', '-0.1829', '-0.08203', '0.00872', '-0.3428', '0.01463', '0.346', '-0.1796', '0.01454', '-0.4324', '0.1676', '-0.1724', '0.0183', '-0.167', '0.1106', '-0.02267', '0.04373', '0.06012', '0.1493', '-0.0572', '0.2161', '-0.1926', '0.2085', '-0.1045', '-0.1187', '0.1154', '0.342', '-0.1431', '0.5063', '-0.25', '0.2664', '-0.06256', '-0.1963', '-0.254', '0.1647', '0.3323', '-0.288', '-0.2979', '0.05408', '0.1832', '-0.175', '-0.2203', '0.717', '-0.0596', '0.1094', '-0.1315', '0.3503', '0.3057', '0.4048', '0.1724', '0.555', '0.1763', '0.262', '0.5225', '0.2925', '0.10126', '-0.295', '0.4412', '0.2935']",,,,,,,
mondo:0017284,Xp22.13p22.2 duplication syndrome,"['Duplication Xp22', 'dup(X)(p22.13p22.2)', 'dup(X)(p22)']",,,284180,CN202846,,,,,,,,
mondo:0017285,penoscrotal transposition,"['penoscrotal transposition', 'congenital penoscrotal transposition', 'congenital transposition of the penis', 'Prepenile scrotum', 'penoscrotal transposition (disease)']",,,2842,C1868854,,C99010,,C536650,,,10067287,0100600
mondo:0017286,tempi syndrome,"['telangiectasia-erythrocytosis-monoclonal gammopathy-perinephric-fluid collections-intrapulmonary shunting syndrome', 'telangiectasia - erythrocytosis - monoclonal gammopathy - perinephric-fluid collections - intrapulmonary shunting']",,,284227,C3854394,,C121656,,,,,,
mondo:0017287,IgG4-related disease,"['IgG4-related autoimmune disease', 'IgG4-positive multiorgan lymphoproliferative syndrome', 'IgG4-related systemic disease', 'IgG4-RD', 'Immunoglobulin G4-related sclerosing disease', 'IgG4-syndrome', 'IgG4-related systemic sclerosing disease', 'hyper-IgG4 disease', 'multifocal idiopathic fibrosclerosis', 'systemic IgG4-related plasmacytic syndrome', 'systemic IgG4-related sclerosing syndrome', 'multifocal fibrosclerosis', 'IgG4-related sclerosing disease', 'IgG4-associated disease']",0080356,,596448,C3203653,,C95992,,,,,10071569,
mondo:0017288,DICER1 syndrome,"['pleuropulmonary blastoma familial tumour susceptibility syndrome', 'DICER1 syndrome', 'pleuropulmonary blastoma familial tumor susceptibility syndrome', 'DICER1-related pleuropulmonary blastoma cancer predisposition syndrome', 'PPB familial tumour susceptibility syndrome', 'PPB familial tumor susceptibility syndrome', 'pleuro-pulmonary blastoma familial tumor susceptibility syndrome', 'pleuro-pulmonary blastoma familial tumour susceptibility syndrome', 'PPBFTDS', 'DICER1-related pleuropulmonary blastoma']",0081063,,284343,CN240512,,C123317,0009068,,199.1,,,
mondo:0017289,fetal lung interstitial tumor,"['flit', 'immature interstitial mesenchymal tumour', 'immature interstitial mesenchymal tumor']",,,284362,CN202863,,,,,,,,
mondo:0017290,familial intrahepatic cholestasis,['hereditary intrahepatic cholestasis'],,,284385,CN239338,,,,,576.8,,,
mondo:0017291,reversible cerebral vasoconstriction syndrome,['RCVS'],,,284388,C3544214,,,,,437.8,,,
mondo:0017292,well-differentiated fetal adenocarcinoma of the lung,"['fetal adenocarcinoma', 'WDFA', 'well-differentiated foetal lung adenocarcinoma', 'pulmonary endodermal tumour resembling foetal lung', 'pulmonary adenocarcinoma of foetal type', 'well-differentiated fetal lung adenocarcinoma', 'fetal lung adenocarcinoma', 'foetal lung adenocarcinoma', 'pulmonary adenocarcinoma of fetal type', 'pulmonary endodermal tumor resembling fetal lung', 'foetal adenocarcinoma']",,,284395,CN202865,,C45509,,,,,,
mondo:0017294,"glycerol kinase deficiency, infantile form",,,,284408,,,,,,,,,
mondo:0017295,"glycerol kinase deficiency, juvenile form",,,,284411,,,,,,,,,
mondo:0017296,"glycerol kinase deficiency, adult form",,,,284414,,,,,,,,,
mondo:0017297,chronic lymphocytic inflammation with pontine perivascular enhancement responsive to steroids,['CLIPPERS'],,,284448,C3854437,,,,,,,,
mondo:0017298,acute zonal occult outer retinopathy,['AZOOR'],,,284454,C0730298,,,,C538223,362.10,,,
mondo:0017299,acute annular outer retinopathy,['AAOR'],,,284460,,,,,,,,,
mondo:0017300,congenital pericardium anomaly,,,,2846,,,,,,746.89,,,
mondo:0017301,pericardial and diaphragmatic defect,,,,2847,,,,,,,,,
mondo:0017302,qualitative or quantitative defects of troponin,,,,284786,,,,,,,,,
mondo:0017303,qualitative or quantitative defects of tropomyosin,,,,284790,,,,,,,,,
mondo:0017304,ocular albinism,"['ocular albinism (disease)', 'ocular albinism', 'XLOA']",0050633,,284804,,,,,D016117,270.2,,10065276,0001107
mondo:0017305,syndromic oculocutaneous albinism,"['syndrome associated with oculocutaneous albinism', 'syndromic oculocutaneous albinism']",,,284811,CN227111,,,,,,E70.3,,
mondo:0017306,disorder of phenylalanine metabolism,,,,284814,C0268461,,,,,270.8,,,
mondo:0017307,disorder of tyrosine metabolism,,,,284818,CN202881,,,,,270.2,,,
mondo:0017309,neonatal Marfan syndrome,['neonatal MFS'],,,284979,CN536247,,,,,,,,
mondo:0017310,Marfan and Marfan-related disorder,,,,284993,CN227112,,,,,,,,
mondo:0017312,Perrault syndrome,"['XX gonodal dysgenesis-deafness syndrome', 'gonadal dysgenesis, XX type, with deafness']",0050857,,2855,CN239459,"['0.01727', '-0.05762', '-0.3599', '0.1371', '-0.10706', '-0.4534', '0.1798', '1.241', '-0.5664', '-0.316', '-0.289', '-0.07605', '-0.1504', '0.8013', '0.7915', '-0.0997', '0.5747', '-0.1698', '-0.2239', '-0.517', '-0.1015', '0.1757', '0.136', '-0.5796', '0.304', '-0.1478', '-0.11615', '-0.357', '0.074', '-0.4177', '0.768', '-0.3179', '0.4177', '-0.2761', '-0.3147', '-0.524', '-0.1389', '-0.4773', '-0.5376', '0.366', '0.5425', '0.06976', '0.4502', '0.1037', '0.3604', '-0.2737', '0.1215', '-0.1257', '-1.099', '0.1765', '0.07385', '0.1428', '-1.041', '-0.1866', '-0.2703', '-0.02005', '0.758', '-0.585', '-0.3438', '0.599', '0.03094', '-0.152', '0.2299', '0.535', '-0.5293', '0.1351', '0.008286', '0.511', '-0.495', '0.1567', '-0.3342', '0.2769', '-0.2058', '-0.2837', '0.634', '-0.5312', '0.2189', '-0.3718', '-0.2045', '0.01352', '0.2134', '0.285', '-0.2206', '0.897', '-0.2808', '-0.2433', '0.2761', '0.0716', '0.3325', '0.264', '-0.0918', '0.4817', '0.1343', '-0.1133', '0.8677', '-0.2585', '0.2448', '-0.4973', '0.1943', '-0.518']",,,,,,,
mondo:0017313,disorder of folate metabolism and transport,,,,285657,CN227114,,,,,,,,
mondo:0017314,"Ehlers-Danlos syndrome, vascular type","['Ehlers Danlos syndrome, arterial type', 'EDS type 4 (formerly)', 'Ehlers-Danlos syndrome, type IV', 'Ehlers Danlos syndrome, sack-Barabas type', 'Ehlers-Danlos syndrome type IV (formerly)', 'EDS4 (formerly)', 'EDS IV', 'vascular Ehlers-Danlos syndrome', 'Ehlers Danlos syndrome, ecchymotic type', 'Ehlers-Danlos syndrome type IV', 'EDS IV (formerly)', 'vEDS', 'vascular EDS', 'EDS type 4', 'Ehlers-Danlos syndrome type 4', 'sack-Barabas syndrome', 'Ehlers-Danlos syndrome type 4 (formerly)']",,,286,,"['0.2544', '0.1033', '-0.7954', '0.3303', '-0.06287', '-0.435', '0.1173', '0.807', '-0.686', '0.5884', '-0.347', '0.2058', '0.6294', '0.843', '-0.4177', '0.2247', '-0.6035', '0.559', '0.04892', '-0.626', '-0.229', '0.3586', '0.677', '-0.1312', '-0.353', '0.3352', '0.11584', '0.3848', '1.435', '-0.1315', '1.374', '-0.7285', '-0.09235', '-0.1624', '0.06445', '0.231', '-0.1433', '-0.02306', '0.2145', '-0.6816', '0.5845', '-0.5703', '-0.366', '0.2183', '0.504', '-0.2269', '-0.9556', '0.609', '0.5923', '0.04193', '0.02534', '-0.4016', '0.2925', '-0.00133', '-0.0303', '-0.696', '-0.3298', '0.573', '0.2698', '-0.00858', '-0.1753', '0.3645', '0.1688', '-0.01438', '0.2646', '0.006004', '-0.1575', '0.67', '0.07306', '1.147', '-0.5444', '0.10095', '-0.4978', '-0.2642', '-0.1335', '-0.2494', '-0.2803', '0.00465', '0.2583', '-0.2651', '-0.596', '-0.526', '0.2026', '0.619', '-0.1025', '-0.01199', '0.09784', '0.2173', '0.39', '-0.2216', '0.2896', '0.2299', '-0.5664', '0.0002335', '0.5205', '-0.1392', '0.3667', '-0.1846', '0.2573', '0.2507']",C125699,,,,,,
mondo:0017315,short stature-webbed neck-heart disease syndrome,"['Al Gazali-Aziz-Salem syndrome', 'short stature, intellectual disability, facial dysmorphism, short webbed neck, skin changes and congenital heart disease', 'short stature, webbed neck, heart disease', 'Al Gazali Aziz Salem syndrome']",,,2865,C2930950,,,,C535613,,,,
mondo:0017316,short stature-deafness-neutrophil dysfunction-dysmorphism syndrome,"['thong Douglas Ferrante syndrome', 'short stature deafness neutrophil dysfunction', 'thong-Douglas-Ferrante syndrome']",,,2866,,,,,,,,,
mondo:0017317,phakomatosis pigmentokeratotica,"['Phacomatosis pigmentokeratotica', 'organoid nevus with sebaceous differentiation, a speckled-lentiginous nevus, and other associated anomalies']",,,2874,C2931658,,,,C537893,,,,
mondo:0017318,phakomatosis pigmentovascularis,"['association of cutaneous vascular malformations and different pigmentary disorders', 'Phacomatosis pigmentovascularis', 'PPv']",,,2875,,,,,C537894,709.09,,,
mondo:0017319,hereditary elliptocytosis,"['congenital elliptocytosis', 'ovalocytosis', 'hereditary ovalocytosis', 'HE']",2373,,288,C0013902,"['-0.2278', '0.3804', '-0.05246', '-0.1149', '0.1437', '-0.05905', '-0.3252', '0.613', '0.09357', '-0.2185', '-0.2998', '0.56', '-0.361', '0.452', '-0.2399', '-0.6665', '-0.476', '-0.308', '0.373', '-1.057', '-0.1525', '0.2499', '0.758', '-0.1829', '-0.1395', '-0.03015', '-0.4558', '-0.2494', '0.2146', '-0.05844', '-0.06244', '-0.6035', '0.2451', '0.909', '-0.59', '0.2422', '-0.5103', '-0.2822', '-0.2295', '0.284', '-0.007275', '-0.0462', '0.6235', '-0.2756', '-0.02644', '-0.1248', '-0.7427', '-0.4175', '0.248', '0.2136', '0.3171', '-0.173', '0.11273', '0.3796', '0.2035', '0.316', '0.2903', '-0.2439', '0.1329', '0.221', '-0.03436', '0.1676', '0.4072', '-0.003496', '0.758', '-0.01065', '0.8623', '0.736', '-0.1164', '0.919', '0.4219', '-0.2158', '0.07245', '0.293', '-0.005615', '0.204', '0.4658', '-0.566', '-0.2325', '-0.4414', '-0.1838', '-0.2046', '-0.169', '0.3083', '0.3367', '-0.2974', '-0.171', '0.5684', '0.2443', '-0.314', '1.062', '0.274', '0.4795', '-0.2546', '0.3408', '0.3413', '0.1505', '-0.534', '0.3313', '-0.515']",C35882,,D004612,282.1,D58.1,10014490,
mondo:0017320,phosphoenolpyruvate carboxykinase deficiency,"['PEPCK deficiency', 'phosphoenolpyruvate carboxykinase (GTP) deficiency']",,,2880,C0268194,"['-0.602', '0.04083', '-0.1265', '0.01019', '0.2004', '-0.7104', '-0.252', '0.189', '-0.3867', '-0.00928', '-0.0663', '-0.3105', '-0.12054', '0.08453', '-0.1411', '-0.02629', '0.1042', '-0.1665', '-0.555', '-0.827', '0.3403', '-0.3972', '0.3005', '-0.2155', '0.1761', '-0.3591', '0.03958', '-0.10004', '-0.1444', '-0.0587', '0.0319', '0.6304', '0.1396', '0.4265', '-0.25', '-0.2318', '-0.2332', '0.06616', '-0.2693', '0.2832', '-0.1848', '-0.5186', '0.21', '0.3328', '-0.3337', '-0.3906', '-0.1392', '0.05093', '0.1367', '0.2986', '-0.162', '-0.1431', '0.1726', '0.1549', '0.1741', '-0.4507', '0.3372', '0.1028', '-0.2115', '0.392', '0.0492', '-0.11804', '0.3132', '-0.3105', '-0.322', '-0.2788', '0.3562', '0.4219', '-0.597', '-0.1716', '-0.4045', '-0.09863', '0.2798', '-0.02824', '0.02608', '0.05136', '0.1633', '-0.2573', '-0.3066', '0.1225', '0.436', '-0.118', '-0.2651', '-0.09503', '0.3584', '0.3528', '0.0327', '-0.1083', '0.483', '-0.00797', '0.3645', '0.2542', '-0.16', '-0.2888', '0.3025', '0.867', '0.4', '-0.2886', '0.1147', '-0.001851']",C99015,,C536654,277.89,,,
mondo:0017321,pili torti-onychodysplasia syndrome,,,,2890,C2931483,,,,,,,,
mondo:0017322,disorders of vitamin D metabolism,,,,289098,CN202954,,,,,,,,
mondo:0017323,hypocalcemic rickets,"['calcium deficiency rickets', 'Calciopenic rickets']",,,289103,C4329608,,C131421,,,,,,
mondo:0017324,autosomal recessive hypophosphatemic rickets,"['hereditary hypophosphatemic rickets, autosomal recessive', 'hypophosphatemic rickets, autosomal recessive', 'autosomal recessive hereditary hypophosphatemic rickets', 'ARHR']",0050949,,289176,CN202957,"['0.3704', '-0.0221', '0.2605', '-0.3418', '-0.1218', '-0.03506', '-0.9487', '1.191', '0.207', '0.1661', '0.664', '0.6187', '-0.669', '0.9185', '-0.423', '-0.09283', '-0.04657', '0.05472', '-0.7456', '-0.8677', '-0.223', '-0.776', '0.5645', '-0.3223', '0.0663', '-0.1575', '-0.067', '-0.4558', '0.3352', '-0.2705', '0.314', '-0.2944', '-0.5044', '0.3076', '-0.1255', '-0.1329', '-0.2883', '0.0347', '0.65', '0.2842', '-0.4248', '-0.2291', '-0.832', '0.01071', '0.06805', '-0.5483', '0.4922', '0.0615', '0.2559', '0.6226', '-0.0748', '-0.7153', '0.1724', '0.2524', '-0.528', '-1.049', '-0.2474', '0.2081', '-0.9893', '0.0385', '0.6924', '-0.284', '-0.4048', '0.563', '0.447', '0.7026', '1.161', '1.3', '-0.595', '-0.653', '0.3003', '-0.1947', '0.674', '-0.589', '-0.04617', '1.359', '0.2318', '-0.6416', '0.5527', '0.2468', '0.4072', '0.2659', '0.6904', '-0.1787', '-0.2673', '0.1934', '0.4714', '0.1785', '0.9', '0.395', '0.7744', '0.1503', '-0.4724', '0.2211', '-0.3164', '0.3838', '0.6978', '-0.2512', '-0.578', '-0.1556']",,,,,E83.3,,
mondo:0017325,early-onset epileptic encephalopathy and intellectual disability due to GRIN2A mutation,,,613971,289266,,,,,,,,,
mondo:0017326,infective dermatitis associated with HTLV-1,"['IDH Gene family', 'infective dermatitis associated with human T-lymphotropic virus type 1', 'IDH', 'isocitrate dehydrogenase Gene family', 'infective dermatitis associated with human T-lymphotropic virus type I']",,,289347,CN202966,,C129260,,,,,,
mondo:0017327,primary non-gestational choriocarcinoma of ovary,"['NGCO', 'primary non-gestational ovarian choriocarcinoma']",,,289356,CN202967,,,,,,,,
mondo:0017328,non-central nervous system-localized embryonal carcinoma,['non-CNS-localized embryonal carcinoma'],,,289362,CN202968,,,,,,,,
mondo:0017329,familial vesicoureteral reflux,"['familial VUR', 'hereditary vesicoureteral reflux (disease)']",,,289365,CN202969,,,,,,,,
mondo:0017330,malignancy diagnosed during pregnancy,['cancer diagnosed during pregnancy'],,,289385,CN227116,,,,,,,,
mondo:0017331,Pilotto syndrome,"['cleft lip and palate, congenital heart disease, scoliosis, short stature, and mental retardation', 'cleft lip and palate, congenital heart disease, scoliosis, short stature, and intellectual disability']",,,2894,C2931484,,,,C537400,,,,
mondo:0017332,pyoderma gangrenosum-acne-suppurative hidradenitis syndrome,['pash syndrome'],,,289478,CN202977,,,0009009,,,,,
mondo:0017334,12q15q21.1 microdeletion syndrome,"['monosomy 12q15q21.1', 'deletion 12q15q21.1', 'Del(12)(q15)(q21.1)']",,,289513,CN202984,,,,,,,,
mondo:0017335,microtriplication 11q24.1,['tetrasomy 11q24.1'],,,289522,,,,,,,,,
mondo:0017336,fatal infantile hypertrophic cardiomyopathy due to mitochondrial complex I deficiency,"['fatal infantile hypertrophic cardiomyopathy due to NADH-CoQ reductase deficiency', 'fatal infantile HCM due to mitochondrial complex I deficiency', 'fatal infantile hypertrophic cardiomyopathy due to NADH-coenzyme Q reductase deficiency']",,,289527,,,,,,,,,
mondo:0017337,inherited isolated adrenal insufficiency due to partial CYP11A1 deficiency,,,,289548,,,,,,,,,
mondo:0017338,fatal multiple mitochondrial dysfunctions syndrome,"['fatal multiple mitochondrial dysfunction syndrome', 'multiple mitochondrial dysfunctions syndrome', 'MMDS']",0070330,,289573,CN234684,"['-0.3362', '0.2241', '-0.1666', '-0.02469', '-0.06665', '-0.505', '-0.10034', '0.3125', '-0.1792', '-0.3015', '-0.1411', '-0.4885', '0.2068', '0.06494', '0.11383', '-0.2355', '-0.3203', '0.05505', '-0.534', '-0.2922', '0.2318', '-0.3687', '0.6255', '-0.1631', '0.3025', '-0.268', '-0.02888', '0.2815', '0.0256', '0.2961', '0.503', '0.1974', '0.8433', '0.4014', '-0.1821', '0.1716', '-0.2148', '0.04794', '-0.1088', '-0.06012', '0.1093', '-0.333', '0.07874', '0.4355', '0.1287', '-0.1788', '-0.10156', '-0.2737', '-0.1193', '-0.0361', '-0.1117', '0.03503', '-0.10406', '-0.1593', '0.1371', '-0.1895', '0.2181', '-0.0214', '-0.1761', '0.506', '0.0931', '-0.07526', '0.454', '0.3105', '-0.5806', '-0.1962', '0.521', '0.3877', '-0.2476', '0.3408', '-0.01872', '0.6143', '-0.2047', '-0.0461', '-0.08044', '0.05032', '0.444', '0.02145', '-0.644', '-0.127', '0.4358', '0.14', '-0.1267', '0.0913', '-0.0391', '0.2507', '0.2415', '0.1141', '0.4272', '0.0705', '0.5425', '0.3542', '-0.10925', '0.08136', '0.257', '0.3354', '0.281', '0.3445', '0.1213', '0.4192']",,,C565304,,,,
mondo:0017339,exfoliative ichthyosis,"['ichthyosis exfoliativa', 'autosomal recessive exfoliative ichthyosis']",,,289586,C1838440,"['-0.1848', '0.1985', '-0.2898', '-0.2024', '0.02145', '-0.1937', '-0.2163', '-0.2512', '-0.0284', '-0.05182', '0.2123', '0.2345', '-0.2668', '-0.336', '-0.844', '-0.00374', '0.597', '-0.4229', '0.01018', '-0.978', '-0.3806', '-0.0764', '0.452', '-0.068', '0.3645', '0.438', '0.194', '-0.1825', '-0.4302', '0.0548', '0.3303', '-0.0421', '0.376', '0.1847', '0.536', '0.742', '-0.5605', '-0.1432', '0.551', '-0.821', '0.001913', '-0.4666', '0.02914', '0.282', '-0.3682', '-0.544', '-0.203', '0.01883', '0.269', '0.0519', '-0.11957', '-0.08655', '0.4683', '0.153', '-0.57', '0.3364', '1.119', '0.4653', '-0.557', '-0.3308', '-0.1619', '-0.0471', '-0.09094', '0.0754', '-0.0834', '-0.357', '0.5713', '0.4878', '-0.03537', '0.993', '-0.529', '-0.0862', '-0.2343', '0.3423', '0.0538', '-0.05844', '0.3208', '-0.1858', '0.2988', '-0.4766', '-0.0311', '-0.6323', '0.3862', '0.2693', '0.1129', '-0.615', '-0.976', '1.117', '0.2612', '0.1819', '0.7095', '0.89', '0.3606', '0.3723', '0.2296', '0.3894', '0.5435', '-0.8965', '-0.05984', '-0.2825']",,,,,,,
mondo:0017340,juvenile nasopharyngeal angiofibroma,"['nasopharyngeal angiofibroma', 'juvenile nasopharyngeal angiofibroma (disease)', 'JNA', 'juvenile nasopharyngeal angiofibroma', 'nasopharyngeal juvenile angiofibroma']",,,289596,CN202999,,C27479,,,,D10.6,,0030429
mondo:0017341,virus associated tumor,,,,289635,CN203003,,,,,,,,
mondo:0017342,Epstein-Barr virus-related tumor,"['EBV-related tumor', 'EBV-related tumour']",,,289638,CN203004,,,,,,,,
mondo:0017343,Epstein-Barr virus-associated malignant lymphoproliferative disorder,['EBV-associated lymphoproliferative disorder'],,,289644,C2363744,,,,,,,10068349,
mondo:0017344,Epstein-Barr virus-associated carcinoma,['EBV-associated carcinoma'],,,289651,,,,,,,,,
mondo:0017345,Epstein-Barr virus-associated mesenchymal tumor,"['EBV-associated mesenchymal tumour', 'EBV-associated mesenchymal tumor']",,,289656,CN203006,,,,,,,,
mondo:0017346,Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly,"['EBV Positive diffuse large B-cell lymphoma of the elderly', 'Epstein-Barr Virus Positive diffuse large B-cell lymphoma of the elderly', 'Senile EBV-associated B-cell lymphoproliferative disorder', 'age-related EBV Positive B-cell lymphoproliferative disorder', 'EBV-positive DLBCL of the elderly', 'EBV-Positive diffuse large B-cell lymphoma, NOS']",,,289661,C2700007,,C80281,,,,,,
mondo:0017347,plasmablastic lymphoma,"['Plasmablastic lymphoma', 'PLBL', 'PBL']",0080779,,289666,C3472614,,C7224,,D000069293,,,10065039,
mondo:0017348,lymphoepithelial-like carcinoma,,,,289682,,,,,,,,,
mondo:0017349,myopericytoma,"['hemangiopericytoma', 'MPC', 'solitary myofibroma']",,,289685,C1302808,,C50401,,D000077777,,,,
mondo:0017350,inborn disorder of tryptophan metabolism,"['inborn error of tryptophan metabolic process', 'disorder of tryptophan metabolism', 'rare inborn error of tryptophan metabolic process']",,,289829,CN203012,,,,,270.2,,,
mondo:0017351,inborn disorder of lysine and hydroxylysine metabolism,['disorder of lysine and hydroxylysine metabolism'],,,289832,,,,,,270.8,E72.3,,
mondo:0017352,disorder of glutamine metabolism,,,,289841,C0342669,,,,,270.7,,,
mondo:0017353,neonatal glycine encephalopathy,"['neonatal non-ketotic hyperglycinemia', 'neonatal NKH', 'classic glycine encephalopathy']",,,289857,,"['0.1472', '0.54', '-0.2932', '0.2137', '-0.749', '-0.771', '0.6665', '0.674', '-0.3428', '-0.682', '-0.35', '-0.527', '0.05725', '0.174', '0.06216', '-0.3572', '0.2559', '-0.2905', '0.0541', '-0.484', '-0.01189', '0.03745', '0.4744', '-0.289', '0.09717', '-0.2668', '-0.02066', '-0.3071', '-0.5396', '0.3767', '0.312', '-0.1901', '0.3562', '0.529', '0.05695', '0.07825', '-0.4548', '-0.518', '-0.0543', '0.3845', '0.1312', '-0.5845', '0.02513', '-0.09644', '0.0317', '0.2369', '-0.4224', '0.1729', '-0.354', '1.08', '-0.51', '0.04617', '-0.2952', '-0.1615', '-0.2394', '0.383', '-0.4548', '-0.1964', '-0.24', '0.5293', '0.0634', '-0.3997', '0.04675', '-0.1377', '-0.3286', '-0.004864', '0.3655', '0.3518', '-0.1436', '0.5103', '0.2834', '0.1794', '0.2808', '-0.02058', '0.2656', '0.4924', '0.08405', '-0.267', '-0.2045', '0.1891', '-0.1351', '-0.0968', '-0.4314', '-0.04462', '0.3367', '0.572', '-0.2142', '0.2015', '0.536', '0.4717', '0.4243', '0.1582', '-0.1661', '0.3691', '0.02249', '0.4414', '0.1327', '-0.606', '0.399', '-0.0761']",,,,,,,
mondo:0017354,infantile glycine encephalopathy,"['infantile onset glycine encephalopathy', 'infantile NKH', 'glycine encephalopathy of infancy', 'infantile non-ketotic hyperglycinemia']",,,289860,,,,,,,,,
mondo:0017355,inborn disorder of proline metabolism,"['disorder of proline metabolism', 'rare inborn error of proline metabolic process', 'inborn error of proline metabolic process']",,,289866,CN227118,,,,,,,,
mondo:0017356,inborn disorder of ornithine metabolism,"['inborn error of ornithine metabolic process', 'rare inborn error of ornithine metabolic process', 'disorder of ornithine metabolism']",,,289869,C0342690,,,,,,,,
mondo:0017357,transient hyperammonemia of the newborn,,,,289877,CN203020,,,,,,,,
mondo:0017359,3-methylglutaconic aciduria,,0060336,,289902,C3696376,"['-0.2231', '0.245', '0.003485', '0.03333', '0.171', '-0.1455', '-0.2179', '0.2854', '-0.2394', '0.0629', '-0.1917', '-0.157', '0.1299', '-0.10626', '-0.1316', '-0.067', '0.0385', '0.05585', '-0.2986', '-0.4807', '0.05954', '-0.2307', '0.2605', '-0.07074', '0.0868', '-0.0788', '-0.0196', '-0.0452', '-0.3108', '0.05173', '0.3198', '0.06573', '0.1841', '0.0488', '-0.1464', '-0.001769', '-0.0985', '-0.07635', '-0.142', '-0.2284', '-0.01672', '-0.585', '0.1897', '-0.1197', '-0.393', '-0.3257', '0.2637', '-0.069', '0.3386', '0.1592', '-0.166', '-0.08295', '0.00927', '-0.2295', '0.0806', '-0.1923', '0.4336', '0.1057', '-0.4336', '0.1854', '0.2142', '-0.03995', '0.3884', '-0.04245', '-0.1783', '0.02916', '0.1953', '-0.05338', '-0.4822', '0.1655', '-0.05435', '0.0833', '-0.1232', '0.05173', '0.2693', '0.283', '0.1984', '0.1842', '-0.1442', '-0.0776', '0.2095', '-0.10614', '0.05582', '0.04584', '0.067', '0.02618', '0.06107', '0.3394', '0.165', '-0.05933', '0.0888', '0.2225', '-0.2183', '-0.091', '0.266', '0.4524', '0.1641', '-0.2712', '-0.2179', '0.254']",C98678,,C579867,,E71.111,,
mondo:0017360,vitamin B12-unresponsive methylmalonic acidemia type mut0,"['complete deficiency of methylmalonyl-CoA mutase', 'vitamin B12-unresponsive methylmalonic aciduria type mut0']",,,289916,CN203025,"['-0.04822', '0.0987', '-0.4204', '-0.1371', '-0.0963', '-0.518', '-0.1533', '0.263', '0.00982', '0.1193', '-0.3687', '-0.4614', '0.005657', '0.1827', '-0.4343', '-0.3328', '-0.07074', '-0.0791', '-0.0827', '-0.895', '0.0167', '-0.2837', '0.3047', '-0.1896', '0.1814', '-0.2559', '0.1957', '-0.2357', '0.02805', '-0.0937', '0.1655', '0.05243', '0.3762', '0.4', '-0.227', '0.1823', '-0.1489', '-0.3845', '-0.1019', '0.55', '0.04065', '-0.4236', '0.2988', '0.3428', '-0.0493', '-0.1343', '-0.04984', '-0.0428', '-0.582', '0.2927', '-0.2986', '0.1656', '0.0674', '-0.3523', '-0.1076', '-0.05557', '0.10864', '-0.0426', '-0.2144', '0.56', '-0.04288', '0.1328', '0.09845', '-0.301', '0.0568', '-0.07275', '0.227', '0.4272', '-0.4683', '0.521', '0.0882', '-0.04013', '-0.1781', '-0.5483', '0.03293', '0.255', '-0.00552', '-0.5405', '-0.1254', '0.3203', '0.4197', '-0.1743', '-0.1545', '-0.2588', '0.625', '0.4863', '-0.02141', '0.3206', '0.5786', '0.2913', '0.7104', '0.4048', '0.01624', '-0.299', '0.4043', '1.02', '0.4373', '-0.3264', '-0.002197', '0.1982']",,,,,,,
mondo:0017361,congenital rubella syndrome,"['rubella congenital', 'congenital rubella syndrome', 'mother-to-child transmission of rubella syndrome', 'fetal rubella syndrome', 'foetal rubella syndrome', 'congenital rubella', 'CRS']",,,290,C0035921,,C34992,0007218,D012410,771.0,P35.0,10010618,
mondo:0017362,neuralgic amyotrophy,"['mononeuritis multiplex with brachial predilection', 'neuralgic shoulder amyotrophy', 'immune brachial plexus neuropathy', 'acute brachial plexus neuritis', 'brachial plexus neuritis']",,,2901,,,,,,,,10063020,
mondo:0017363,idiopathic chronic eosinophilic pneumonia,"['Carrington^s pulmonary eosinophilia', 'eosinophilic idiopathic chronic pneumopathy', 'chronic eosinophilic pneumonia (CEP)', 'Carrington^s disease', 'Carrington syndrome', 'chronic idiopathic eosinophilic pneumonia', 'chronic eosinophilic pneumonia']",,,2902,,,,,C535590,,,,
mondo:0017364,POEMS syndrome,"['polyneuropathy organomegaly', 'polyneuropathy, organomegaly, endocrinopathy, M protein, and skin changes syndrome', 'Takatsuki syndrome', 'osteosclerotic myeloma', 'Crow-Fukase syndrome', 'polyneuropathy-endocrinopathy-plasma cell dyscrasia syndrome', 'PEP syndrome', 'POEMS syndrome']",14039,,2905,C0085404,,C80303,1001115,D016878,,,10053869,
mondo:0017365,"hereditary acrokeratotic poikiloderma, Weary type","['congenital poikiloderma with bullae, Weary type']",,,2907,,,,,,,,,
mondo:0017366,hereditary pheochromocytoma-paraganglioma,"['hereditary paraganglioma-pheochromocytoma', 'SDHx-related paraganglioma-pheochromocytoma', 'familial pheochromocytoma-paraganglioma']",,,29072,C1708353,"['-0.2034', '0.7393', '-0.0759', '-0.304', '-0.5947', '0.2908', '0.4148', '0.629', '-0.4265', '-0.3313', '0.335', '0.05212', '-0.09973', '0.0693', '-0.515', '0.1329', '-0.861', '-0.1865', '-0.02129', '0.05185', '-0.1031', '-0.563', '0.4783', '0.0742', '0.0962', '0.2274', '-0.2007', '-0.569', '0.249', '-0.4368', '0.462', '0.2615', '0.4226', '-0.10547', '-0.8027', '-0.1409', '-0.657', '0.4834', '-0.00454', '-0.586', '0.1525', '-0.0901', '0.2415', '-0.284', '0.9185', '-0.368', '-0.05682', '0.1678', '0.5107', '-0.0777', '-0.0816', '0.2438', '-0.0009594', '-0.0755', '-0.04156', '0.2852', '0.1068', '0.3242', '-0.3167', '-0.1534', '-0.4448', '0.1365', '-0.01794', '-0.3533', '-0.4321', '0.798', '0.4363', '0.4395', '0.05045', '0.5645', '0.434', '0.2437', '-0.0476', '-0.4373', '-0.1335', '0.828', '-0.0335', '0.752', '0.04486', '-0.7705', '-0.04196', '-0.10016', '-0.0735', '-0.342', '0.1632', '-0.265', '1.004', '0.11426', '0.279', '-0.02188', '-0.325', '-0.226', '0.3276', '-0.2517', '0.8003', '0.1351', '0.1775', '0.11523', '-0.4817', '0.671']",,,,,,,
mondo:0017372,congenital varicella syndrome,"['fetal varicella zoster syndrome', 'mother-to-child transmission of varicella syndrome', 'fetal effects of chickenpox', 'foetal varicella infection', 'antenatal varicella virus infection', 'foetal varicella zoster syndrome', 'foetal effects of varicella zoster virus', 'fetal varicella infection', 'Varicella embryopathy', 'Varicella virus antenatal infection', 'foetal effects of chickenpox', 'fetal effects of varicella zoster virus']",,,291,C0343560,,C116800,,,771.2,,,
mondo:0017373,poliomyelitis,"['poliomyelitis', 'polio', 'acute poliomyelitis', 'Polia', 'infantile paralysis']",4953,,2912,C0032371,,C35550,0007450,D011051,045.92,,10036012,
mondo:0017375,congenital enterovirus infection,"['antenatal enterovirus infection', 'congenital enterovirus infectious disease', 'mother-to-child transmission of enterovirus infection']",,,292,C4274223,,,,,,,,
mondo:0017376,reactive arthritis,"['Fiessinger-Leroy-Reiter syndrome', 'Reiter syndrome', 'Reiter^s syndrome', 'Reiter disease', 'post-infectious reactive arthropathy', 'polyarthritis enterica', 'post-infectious arthritis', 'Reiter^s disease', 'post-bacterial arthropathy', 'PIRA', 'Fiessinger Leroy Reiter syndrome', 'reactive arthritis', 'venereal arthritis', 'Fiessinger-Leroy disease', 'arthritis urethritica', 'postdysenteric arthropathy']",6196,,29207,CN203069,,C128332,0007460,D016918,711.40,,10038294,
mondo:0017377,preaxial polydactyly-colobomata-intellectual disability syndrome,"['Pfeiffer-Mayer syndrome', 'Pfeiffer Mayer syndrome', 'short stature intellectual disability type I preaxial polydactyly with colobomatous abnormalities', 'short stature mental retardation type I preaxial polydactyly with colobomatous abnormalities']",,,2921,C2931655,,,,C537888,,,,
mondo:0017379,polyneuropathy-intellectual disability-acromicria-premature menopause syndrome,"['polyneuropathy - intellectual deficit - acromicria - premature menopause', 'polyneuropathy intellectual disability acromicria premature menopause', 'Lundberg syndrome', 'polyneuropathy mental retardation acromicria premature menopause']",,,2928,CN203094,,,,,,,,
mondo:0017380,juvenile polyposis syndrome,"['polyposis familial of entire gastrointestinal tract', 'juvenile multiple polyps syndrome', 'juvenile polyposis syndrome', 'juvenile polyposis', 'jPS', 'polyposis, juvenile intestinal', 'juvenile gastrointestinal polyposis', 'polyposis juvenile intestinal', 'PJI', 'juvenile intestinal polyposis', 'JIP']",,174900,2929,CN239474,,C7754,,,,,,
mondo:0017381,congenital herpes simplex virus infection,"['antenatal herpes simplex virus infection', 'Simplexvirus caused infectious embryofetopathy', 'mother-to-child transmission of herpes simplex virus infection', 'neonatal HSV infection', 'neonatal herpes simplex virus infection']",,,293,C0276225,,,,,771.2,,,
mondo:0017382,familial clubfoot due to 5q31 microdeletion,['hereditary clubfoot due to 5q31 microdeletion'],,,293144,CN203109,,,,,,,,
mondo:0017383,familial clubfoot due to PITX1 point mutation,['hereditary clubfoot due to PITX1 point mutation'],,,293150,CN203110,"['-0.174', '-0.2634', '0.365', '0.669', '0.4524', '-0.4385', '-0.1666', '0.7188', '-1.186', '-0.5786', '0.4253', '0.1658', '-0.2563', '1.013', '0.3445', '0.05515', '-0.3447', '0.2878', '-0.1823', '-1.13', '0.03412', '0.674', '-0.259', '-0.3062', '0.0757', '-0.1266', '0.3188', '0.3547', '0.351', '0.2856', '0.262', '-0.787', '0.2512', '0.4626', '-0.298', '0.00921', '-0.0596', '-0.2416', '0.6777', '-0.673', '0.4705', '0.7646', '-0.4043', '0.5347', '0.0425', '0.475', '0.31', '0.126', '0.2175', '0.1989', '-0.2393', '-0.8994', '0.2323', '0.02249', '-0.728', '0.5435', '-0.6396', '0.0304', '-0.2365', '-0.359', '0.2496', '0.1599', '0.0437', '0.4924', '-0.1377', '1.093', '0.3235', '0.03406', '-0.11957', '0.449', '-0.01442', '0.6084', '0.08356', '-0.6226', '0.3242', '0.703', '-0.2076', '0.02933', '-0.1376', '-0.4463', '-0.425', '0.4827', '0.376', '0.413', '0.398', '0.2147', '0.1287', '-0.4487', '1.175', '0.272', '-0.3022', '-0.0404', '-0.0458', '0.2515', '0.6255', '0.63', '0.1032', '-0.3584', '-0.1617', '-0.3115']",,,,,,,
mondo:0017384,acute generalized exanthematous pustulosis,"['toxic pustuloderma', 'AGEP', 'pustular drug eruption']",,,293173,C0877055,,C112122,,D056150,709.8,,10048799,
mondo:0017385,malignant migrating partial seizures of infancy,"['MPSI', 'MPEI', 'migrating partial seizures of infancy', 'MMPSI', 'MMPEI', 'migrating partial epilepsy of infancy', 'migrating Partial seizures in infancy', 'malignant migrating partial epilepsy of infancy', 'malignant migrating Partial seizures in infancy']",,,293181,CN240507,"['0.2252', '-0.00759', '-0.2444', '0.2327', '-0.494', '-0.314', '0.793', '0.314', '-0.4238', '-0.4033', '-0.3923', '-0.01051', '0.0655', '0.728', '-0.3196', '0.2236', '-0.2964', '-0.1992', '-0.198', '-0.611', '-0.2114', '0.7056', '0.1392', '-0.226', '0.0848', '-0.1367', '-0.156', '-0.08215', '-0.4895', '0.5625', '0.04153', '0.1392', '0.3223', '0.4463', '0.3953', '0.6475', '0.01061', '-0.3325', '0.11163', '-0.3506', '-0.05133', '-0.4062', '-0.3708', '-0.3882', '0.136', '-0.4055', '-0.3442', '0.39', '0.2032', '0.821', '-0.04907', '0.2202', '0.1824', '-0.546', '0.11176', '0.12036', '-0.02367', '0.01872', '-0.0485', '-0.08716', '-0.206', '0.3933', '0.555', '-0.02527', '-0.6313', '1.134', '0.4485', '-0.0715', '-0.814', '0.916', '0.577', '0.465', '0.1223', '-0.6484', '0.2961', '0.5923', '0.8193', '0.482', '-0.2964', '-0.101', '0.1455', '0.814', '0.5356', '0.1857', '0.5127', '0.00881', '0.04883', '0.8184', '0.657', '0.926', '0.0865', '0.2316', '0.1178', '0.04224', '-0.1405', '0.0497', '0.01299', '-0.4138', '0.228', '0.308']",C125387,,,,,,
mondo:0017386,pleomorphic rhabdomyosarcoma,"['pleomorphic rhabdomyosarcoma, adult type', 'pleomorphic rhabdomyosarcoma', 'anaplastic rhabdomyosarcoma']",3250,,293199,C0334480,,C4258,,,171.9,,,
mondo:0017387,epithelioid sarcoma,"['ES', 'epithelioid cell sarcoma', 'epithelioid sarcoma']",6193,,293202,C0205944,,C3714,,,,,10015099,
mondo:0017388,celiac trunk compression syndrome,['Dunbar syndrome'],,,293208,CN203119,,,,,,,,
mondo:0017389,tetrahydrobiopterin-responsive hyperphenylalaninemia/phenylketonuria,"['BH4-responsive HPA/PKU', 'tetrahydrobiopterin-responsive HPA/PKU', 'BH4-responsive hyperphenylalaninemia/phenylketonuria']",,,293284,,,,,,,,,
mondo:0017391,Grayson-Wilbrandt corneal dystrophy,['GWCD'],,,293375,,,,,,,,,
mondo:0017392,pre-descemet corneal dystrophy,['PDCD'],,,293462,,,,,,371.56,,,
mondo:0017393,blepharophimosis - intellectual disability syndrome,"['blepharophimosis intellectual disability syndromes', 'blepharophimosis mental retardation syndromes', 'BMRS', 'blepharophimosis syndrome Ohdo type', 'Say Barber Biesecker Young-Simpson syndrome', 'SBBYS syndrome', 'Young Simpson syndrome']",,,293642,CN203134,,,,,,,,
mondo:0017394,ketamine-induced biliary dilatation,,,,293807,CN227122,,,,,,,,
mondo:0017395,fixed pigmented erythema,['fixed drug eruption'],,,293812,,,,,,,,10048796,
mondo:0017396,toxic dermatosis,,,,293815,,,,,,,,,
mondo:0017397,constitutional dyserythropoietic anemia,,,,293830,,,,,,,,,
mondo:0017398,3MC syndrome,"['craniofacial-ulnar-renal syndrome', 'Malpuech-Michels-Mingarelli-Carnevale syndrome', 'oculopalatoskeletal syndrome']",0060225,,293843,CN230015,"['0.5645', '-0.4792', '0.728', '-0.4827', '0.4575', '-0.4011', '0.2612', '1.121', '-0.4165', '-0.5854', '0.3018', '-0.662', '-0.0526', '0.0759', '-0.2109', '0.4531', '-0.6094', '-0.7695', '-0.2551', '-1.013', '0.335', '0.0703', '0.5', '-0.1997', '0.2163', '0.1359', '-0.573', '-0.091', '0.9546', '-0.1014', '0.3096', '0.05118', '0.587', '0.6084', '-0.4023', '-0.2534', '0.4158', '-0.2944', '-0.1917', '-0.1825', '0.2644', '-0.4194', '-0.1453', '-0.2632', '0.6035', '-0.4897', '0.2108', '0.0555', '-0.324', '0.1279', '-0.506', '-0.3074', '-0.2246', '-0.003487', '-0.638', '-0.3557', '0.0308', '0.2156', '0.07745', '0.1339', '0.04578', '0.01973', '0.1821', '0.304', '-0.36', '-0.465', '0.397', '0.3745', '-0.4907', '-0.0808', '-0.314', '0.9556', '-0.1761', '0.2067', '-0.2837', '0.3203', '0.0583', '-0.703', '-0.547', '-0.2169', '0.373', '0.464', '-0.2937', '0.7188', '-0.1917', '0.3013', '0.2495', '-0.2788', '-0.2952', '0.1942', '0.3474', '0.3914', '0.0882', '0.2664', '0.976', '0.0982', '0.3843', '-0.07623', '0.7373', '-0.1857']",,,,,,,
mondo:0017399,"frontotemporal dementia, right temporal atrophy variant","['RTLA', 'rvFTD']",,,293848,CN203142,,,,,,,,
mondo:0017400,hypoplastic pancreas-intestinal atresia-hypoplastic gallbalder syndrome,"['Mitchell-Riley syndrome', 'MTCHRS', 'hypoplastic pancreas-intestinal atresia-hypoplastic gallbladder syndrome', 'diabetes, neonatal, with pancreatic hypoplasia, intestinal atresia, and gallbladder aplasia or hypoplasia']",,615710,293864,C2748662,"['-0.1866', '-0.02345', '0.4138', '-0.2598', '0.0522', '-0.2637', '-0.03146', '0.2386', '-0.07043', '-0.2156', '-0.4116', '-0.2686', '-0.1451', '0.03476', '-0.6045', '-0.2426', '0.088', '0.1848', '-0.152', '-0.7163', '0.1886', '-0.2465', '0.273', '-0.3184', '0.0945', '-0.1279', '0.02007', '0.1841', '0.665', '-0.5015', '0.3298', '-0.217', '0.328', '0.2644', '0.1194', '-0.0769', '-0.0651', '-0.0827', '-0.0831', '0.295', '-0.3274', '0.06635', '0.1952', '0.0678', '-0.3706', '-0.3337', '0.00891', '0.0737', '-0.2252', '0.2421', '-0.3909', '0.2052', '0.3967', '-0.1357', '-0.4097', '0.1167', '-0.14', '-0.1877', '-0.3308', '0.1337', '0.361', '0.249', '-0.1293', '-0.2252', '0.1532', '-0.2568', '0.3174', '0.326', '-0.2457', '0.4128', '-0.3538', '0.1093', '-0.04364', '-0.09424', '-0.1552', '-0.535', '0.3445', '-0.1473', '-0.1676', '0.005535', '-0.3743', '0.2356', '-0.06235', '0.0823', '-0.06192', '0.06195', '0.08203', '0.17', '0.3552', '-0.1683', '0.3535', '0.3462', '0.0804', '-0.1323', '0.4763', '0.03455', '0.2423', '-0.3613', '0.2493', '0.3574']",,,,,,,
mondo:0017401,"familial isolated arrhythmogenic ventricular dysplasia, left dominant form","['familial isolated arrhythmogenic ventricular cardiomyopathy, left dominant form']",,,293888,CN203145,,,,,,,,
mondo:0017402,"familial isolated arrhythmogenic ventricular dysplasia, biventricular form","['familial isolated arrhythmogenic ventricular cardiomyopathy, biventricular form']",,,293899,CN203146,,,,,,,,
mondo:0017403,"familial isolated arrhythmogenic ventricular dysplasia, right dominant form","['familial isolated arrhythmogenic ventricular cardiomyopathy, right dominant form', 'familial isolated arrhythmogenic ventricular cardiomyopathy, classic form', 'familial isolated arrhythmogenic ventricular dysplasia, classic form']",,,293910,CN203147,,,,,,,,
mondo:0017404,distal Xq28 microduplication syndrome,"['distal dup(X)q(28)', 'distal trisomy Xq28', 'Xq28 Microduplication']",,,293939,CN203151,,,,,,,,
mondo:0017405,1p21.3 microdeletion syndrome,"['monosomy 1p21.3', 'Del(1)p(21.3)']",,,293948,CN203152,,,,,,,,
mondo:0017406,hypogonadotropic hypogonadism-severe microcephaly-sensorineural hearing loss-dysmorphism syndrome,['hypogonadotropic hypogonadism-severe microcephaly-sensorineural deafness-dysmorphism syndrome'],,,293967,CN203156,,,,,,,,
mondo:0017407,deficiency in anterior pituitary function - variable immunodeficiency syndrome,['David syndrome'],,,293978,,,,,,,,,
mondo:0017408,rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation syndrome,"['rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation-neural tumors syndrome', 'ROHHADNET', 'ROHHAD syndrome', 'ROHHAD', 'rapid-onset childhood obesity-hypothalamic dysfunction-hypoventilation-autonomic dysregulation-neural tumours syndrome', 'rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation', 'rapid-onset obesity with hypothalamic dysfunction, hypoventilation, and autonomic dysregulation syndrome', 'rapid-onset obesity with hypothalamic dysfunction, hypoventilation and autonomic dysregulation']",,,293987,CN203158,,C121944,,,,,,
mondo:0017409,fetal cytomegalovirus syndrome,"['congenital Cytomegaloviral infection', 'CMV antenatal infection', 'mother-to-child transmission of cytomegalovirus syndrome', 'antenatal CMV infection', 'congenital cytomegalovirus', 'antenatal cytomegalovirus infection']",,,294,C0349499,,C122427,,,,,,
mondo:0017410,porencephaly,,0060263,,2940,,"['-0.433', '0.1687', '-0.2067', '-0.2004', '-0.2766', '-0.3704', '0.1277', '0.0565', '-1.02', '-0.1449', '-0.582', '-0.647', '0.3875', '0.1415', '0.4905', '0.07715', '-0.1235', '-0.6206', '0.0376', '-0.9233', '-0.10065', '0.05804', '0.4976', '-0.7305', '-0.1249', '-0.21', '0.0955', '0.7495', '0.06915', '0.483', '0.637', '-0.3315', '0.434', '-0.244', '-0.4946', '0.302', '-0.4949', '0.01947', '-0.0532', '-0.1278', '0.936', '-0.154', '0.04105', '-0.2145', '0.4714', '0.1849', '0.4595', '-0.3743', '0.08966', '-0.02507', '0.1025', '-0.0771', '-0.1855', '-0.04666', '-0.1365', '0.3782', '0.1433', '0.11566', '-0.3057', '0.2827', '-0.4922', '-0.609', '0.11816', '-0.374', '-0.463', '-0.3333', '0.7456', '0.007656', '-0.662', '0.01174', '-0.713', '-0.2003', '0.0811', '-0.1069', '-0.0698', '0.2717', '0.4526', '0.1064', '-0.4277', '-0.568', '-0.42', '-0.08185', '-0.2408', '0.2598', '0.264', '0.011024', '-0.03433', '0.4543', '0.012245', '0.07043', '0.1761', '0.3901', '-0.1226', '0.3699', '0.324', '-0.04263', '0.6733', '-0.2244', '0.584', '0.0716']",,,D065708,,,10036172,0002132
mondo:0017411,neonatal inflammatory skin and bowel disease,"['inflammatory skin and bowel disease, neonatal']",,,294023,CN228266,"['-0.0394', '0.2024', '0.0866', '-0.4807', '-0.0597', '-0.272', '-0.02815', '-0.00977', '-0.01023', '0.06885', '-0.03625', '-0.01468', '-0.3235', '0.04938', '-0.3699', '0.002584', '0.3325', '0.1814', '-0.2598', '-0.9453', '-0.1322', '-0.429', '0.3267', '-0.3787', '-0.04526', '-0.04907', '-0.2139', '0.2432', '0.267', '-0.3267', '0.05658', '0.12177', '0.1771', '0.2898', '0.3533', '0.05197', '-0.3018', '0.01584', '-0.2467', '-0.09595', '-0.3123', '-0.3645', '0.1425', '-0.03568', '-0.0729', '-0.2224', '-0.4495', '-0.04822', '0.03473', '0.5146', '-0.562', '0.2058', '0.6084', '0.1628', '-0.2069', '-0.1755', '-0.002165', '-0.2357', '-0.3372', '-0.2695', '0.3323', '0.652', '-0.346', '-0.1375', '0.6187', '-0.1947', '0.5117', '0.3855', '-0.02713', '0.4702', '-0.4377', '-0.3342', '-0.12006', '-0.2134', '-0.275', '-0.3928', '0.3186', '-0.02408', '0.1866', '0.05548', '-0.2114', '-0.2393', '0.014305', '-0.08344', '-0.0009384', '-0.04477', '0.1676', '0.2932', '0.2544', '0.0481', '0.3167', '0.192', '0.07776', '0.2422', '0.3796', '0.5044', '0.1967', '-0.1458', '0.203', '0.2341']",,,,,,,
mondo:0017413,Reunion island Larsen syndrome,"['multiple joint dislocations-short stature-hyperlaxity-craniofacial dysmorphism syndrome', 'RLS']",,,294049,CN203163,,,0002319,,,,,
mondo:0017415,multiple pterygium syndrome,['pterygium syndrome'],0080110,,294060,,,,,C537377,755.8,,,
mondo:0017416,postpoliomyelitis syndrome,"['post-polio sequelae', 'postpolio syndrome', 'post-poliomyelitic syndrome', 'postpoliomyelitic syndrome', 'postpoliomyelitis sequelae', 'postpolio sequelae', 'post polio syndrome', 'post-polio muscular atrophy', 'polio late effects', 'postpoliomyelitis syndrome']",4952,,2942,C0080040,,,0007454,D016262,,,,
mondo:0017417,renal-hepatic-pancreatic dysplasia,"['Renohepaticopancreatic dysplasia', 'Ivemark^s syndrome', 'Ivemark II syndrome']",0060259,,294415,C2673883,"['-0.4348', '0.06964', '0.239', '-0.3293', '-0.3726', '-0.3762', '-0.4673', '0.5503', '0.11536', '-0.06506', '-0.5605', '-0.813', '0.0346', '-0.08044', '-0.8086', '-0.5327', '-0.2177', '0.1858', '-0.3274', '-0.9067', '0.3904', '-0.06323', '0.809', '-0.3918', '-0.01251', '-0.0572', '-0.1974', '-0.10297', '0.5815', '-0.41', '0.3562', '-0.2969', '0.5293', '0.3755', '0.667', '-0.10455', '-0.1823', '-0.2932', '-0.0894', '-0.09216', '-0.3115', '0.318', '0.1833', '0.522', '-0.6187', '-0.1373', '0.02402', '-0.1937', '0.2212', '-0.272', '0.02469', '0.4604', '0.098', '0.4377', '-0.4705', '-0.2522', '0.1236', '-0.274', '-0.37', '-0.006393', '0.6343', '0.07794', '-0.2944', '-0.137', '-0.3245', '-0.3376', '0.591', '0.8066', '-0.683', '0.4824', '0.05264', '0.02528', '0.594', '0.4712', '-0.1609', '-0.481', '0.08704', '0.2908', '-0.493', '-0.10266', '-0.11115', '0.6147', '0.2002', '-0.1121', '-0.5317', '-0.185', '0.4233', '0.584', '0.2878', '-0.309', '0.746', '0.461', '0.2812', '0.2031', '0.663', '-0.3616', '0.294', '-0.4111', '0.1958', '0.2472']",,,,,,,
mondo:0017418,chronic intestinal failure,['CIF'],,,294422,CN203168,,,,,,,,
mondo:0017419,non-syndromic amelia,"['nonsyndromic amelia', 'amelia', 'isolated amelia']",,,294925,,,C34370,,,,,10001926,0009827
mondo:0017420,intercalary limb defects,['intercalary meromelia'],,,294927,,,,,,,,,
mondo:0017421,non-syndromic terminal limb defects,"['nonsyndromic terminal limb defects', 'terminal limb defects', 'isolated terminal limb defects', 'terminal meromelia']",,,294929,,,,,,,,,
mondo:0017422,adactyly of hand,['fingers absent'],,,294931,,,,,,,,,
mondo:0017423,split hand or/and split foot malformation,,,,294935,,,,,,,,,
mondo:0017424,non-syndromic brachydactyly,"['nonsyndromic brachydactyly', 'isolated brachydactyly', 'brachydactyly']",,,294937,,"['-0.1406', '0.1794', '0.09735', '0.02837', '0.04834', '-0.1659', '0.1692', '0.1527', '-0.09296', '-0.3237', '0.07166', '0.01794', '0.1152', '0.137', '0.01325', '0.02808', '0.06274', '-0.2343', '0.03314', '-0.3965', '-0.12317', '0.1238', '0.11304', '0.00615', '0.1238', '0.05444', '-0.1081', '-0.09814', '-0.0472', '0.02809', '0.0927', '-0.2612', '0.2051', '0.02153', '0.2014', '-0.1114', '0.1875', '-0.04114', '0.006783', '-0.4011', '0.106', '-0.3572', '-0.09595', '0.00763', '0.221', '-0.002077', '-0.003334', '0.373', '0.0905', '0.012566', '-0.01823', '-0.0725', '-0.02174', '0.1617', '-0.0845', '-0.1567', '0.03482', '-0.2502', '-0.09186', '0.09515', '0.094', '0.02084', '-0.0579', '0.1606', '-0.011055', '-0.04117', '0.09534', '-0.00684', '-0.1062', '0.1542', '-0.2205', '0.08093', '0.2996', '-0.1746', '0.02705', '0.338', '-0.173', '-0.2206', '-0.2179', '-0.2305', '0.1644', '0.11145', '-0.05463', '0.2588', '-0.2372', '-0.01907', '-0.2126', '-0.04303', '0.2598', '0.03635', '-0.1759', '0.08905', '-0.05258', '0.262', '0.3198', '0.0894', '0.1309', '-0.3738', '0.11633', '0.1953']",,,,,,,
mondo:0017425,preaxial polydactyly of fingers,['preaxial polydactyly of hand'],,,294939,,,,,,,,,
mondo:0017426,postaxial polydactyly of fingers,['postaxial polydactyly of hand'],,,294942,,,,,,,,,
mondo:0017427,congenital deformities of limbs,,,,294944,,,,,,,,10024500,
mondo:0017428,congenital deformities of fingers,,,,294947,,,,,,,,,
mondo:0017429,joint formation defects,,,,294949,,,,,,,,,
mondo:0017430,non-syndromic congenital joint dislocations,['congenital joint dislocations'],,,294951,,,,,,,,,
mondo:0017431,non-syndromic limb overgrowth,['limb overgrowth'],,,294953,,"['-0.0367', '0.0679', '0.01924', '-0.0464', '0.03638', '-0.09406', '0.03017', '0.0971', '-0.10803', '-0.04565', '-0.007145', '0.0265', '0.02242', '0.05603', '-0.0288', '-0.0328', '-0.0259', '-0.0635', '-0.0387', '-0.12396', '0.01463', '-0.01923', '0.0533', '-0.0151', '0.0371', '-0.0317', '-0.004597', '0.02147', '0.01483', '-0.03894', '0.05676', '-0.013435', '0.0426', '0.02844', '0.04355', '-0.01666', '-0.02132', '-0.01133', '-0.02571', '-0.0511', '0.08105', '-0.07874', '0.02206', '-0.0236', '0.03055', '-0.0669', '-0.04428', '0.06287', '0.01775', '0.02208', '-0.06476', '-0.0463', '-0.0101', '0.01775', '-0.10425', '-0.0447', '0.02177', '-0.05887', '-0.0709', '-0.01817', '0.06125', '-0.00493', '-0.02576', '0.03543', '-0.0415', '0.03152', '0.09', '0.0679', '-0.0879', '0.07043', '-0.09863', '0.03223', '0.03003', '-0.03008', '0.01338', '0.01106', '-0.01662', '0.002264', '-0.02943', '-0.09247', '-0.04434', '-0.007545', '0.007187', '0.11334', '-0.05515', '0.05444', '0.0328', '0.0566', '0.08685', '-0.011894', '-0.001', '0.06107', '0.01368', '0.04022', '0.1705', '0.011406', '0.08514', '-0.10205', '0.001508', '0.0607']",,,,,,,
mondo:0017435,popliteal pterygium syndrome,"['facio-genito-popliteal syndrome', 'PPS']",0060055,,294963,C0265259,,C118786,,C562509,756.89,,,
mondo:0017436,lethal congenital contracture syndrome,['LCCS'],0060558,,294965,CN239241,"['-0.4253', '-0.118', '0.0611', '-0.1976', '0.12384', '-0.528', '0.1159', '0.3855', '-0.651', '-0.2551', '-0.3088', '0.03653', '0.05255', '0.2566', '-0.0669', '-0.0568', '-0.092', '-0.03366', '-0.02937', '-0.5547', '0.05792', '0.0151', '0.698', '-0.0924', '0.2476', '0.3074', '-0.1844', '0.1294', '-0.1741', '-0.0426', '0.1235', '-0.05365', '0.1886', '0.2352', '0.0844', '-0.0174', '-0.2479', '0.1976', '-0.1129', '0.0634', '-0.1759', '-0.2097', '-0.1644', '0.2644', '0.2008', '-0.2335', '0.01955', '0.4058', '0.2064', '-0.2502', '-0.3162', '-0.172', '0.1503', '-0.2269', '-0.254', '-0.493', '0.1338', '-0.0232', '-0.02808', '-0.002935', '0.0975', '-0.01668', '-0.2007', '0.1501', '-0.4238', '-0.10034', '0.31', '0.327', '-0.07043', '0.1803', '0.005203', '0.1896', '0.01304', '-0.0531', '-0.01901', '-0.1432', '0.1371', '-0.07874', '-0.3977', '-0.286', '-0.1552', '0.02176', '0.04633', '0.433', '-0.1586', '-0.1879', '0.1194', '0.356', '0.11346', '-0.3035', '0.2052', '0.2183', '0.2292', '0.1919', '0.26', '0.1477', '0.727', '-0.1475', '0.214', '0.303']",,,,,,,
mondo:0017437,amelia of upper limb,"['forelimb non-syndromic amelia', 'non-syndromic amelia of forelimb']",,,294967,,,,,,,,,0009812
mondo:0017438,amelia of lower limb,"['hindlimb non-syndromic amelia', 'non-syndromic amelia of hindlimb']",,,294969,,,,,,,,,0009818
mondo:0017439,tetra-amelia,"['tetra-amelia, autosomal recessive', 'total amelia', 'tetra-amelia syndrome', 'Tetraamelia, autosomal recessive']",,,294971,,,,,C536498,,,,0003057
mondo:0017440,humeral agenesis/hypoplasia,"['humeral intercalary meromelia', 'congenital hypoplasia of humerus', 'congenital absence of humerus']",,,294973,,,,,,,,,
mondo:0017441,congenital absence of upper arm and forearm with hand present,"['humero-radio-ulnar intercalary transverse meromelia', 'phocomelia']",,,294975,,,C34928,,,,Q71.1,,
mondo:0017442,congenital absence of thigh and lower leg with foot present,['Femorotibiofibular intercalary transverse meromelia'],,,294977,,,,,,755.33,Q72.1,,
mondo:0017443,congenital absence of both forearm and hand,['radio-ulnar terminal transverse meromelia'],,,294979,,,,,,,Q71.2,,
mondo:0017444,congenital absence of both lower leg and foot,['tibiofibular terminal transverse meromelia'],,,294981,,,,,,,Q72.2,,
mondo:0017445,acheiria,['congenital absence of hand'],,,294983,,,,,,,,,
mondo:0017446,apodia,['congenital absence of foot'],,,294986,,,,,,,,,
mondo:0017447,congenital absence/hypoplasia of thumb,"['thumb hypodactyly', 'thumb oligodactyly']",,,294988,,,,,,,,,
mondo:0017448,congenital absence/hypoplasia of fingers excluding thumb,"['digits 2-5 oligodactyly', 'digits 2-5 hypodactyly']",,,294990,,,,,,,,,
mondo:0017449,split hand,"['split hand (disease)', 'ectrodactyly of hand', 'split hand']",,,294992,,,,,,,,,0001171
mondo:0017450,split foot,"['split foot', 'split foot (disease)']",,,294994,,,,,,,,,0001839
mondo:0017451,non-syndromic brachydactyly of fingers,"['manus non-syndromic brachydactyly', 'short fingers', 'non-syndromic brachydactyly of manus']",,,294996,,,,,,,,,
mondo:0017452,non-syndromic brachydactyly of toes,"['pes non-syndromic brachydactyly', 'short toes', 'non-syndromic brachydactyly of pes']",,,294998,,,,,,755.66,,,
mondo:0017453,fetal parvovirus syndrome,"['fifth disease', 'mother-to-child transmission of parvovirus syndrome', 'Human parvovirus B19 caused infectious embryofetopathy', 'Maternofetal infection by parvovirus', 'Parvovirus antenatal infection', 'Parvovirus B19 antenatal infection']",,,295,,,,,C536301,,,,
mondo:0017454,triphalangeal thumb-polysyndactyly syndrome,['TPT-PS syndrome'],,190605,2950,CN203197,,,,,,,,
mondo:0017455,hyperphalangy,"['supernumerary phalanges', 'supernumerary phalanx']",,,295002,,,,,,,,,
mondo:0017456,central polydactyly of fingers,"['central polydactyly', 'mirror hand', 'mesoaxial polydactyly of fingers', 'mesoaxial polydactyly', 'central polydactyly of hand']",,,295004,,,,,,,,,
mondo:0017457,Preaxial polydactyly of toes,"['bifid great toes', 'bifid hallux', 'preaxial polydactyly of foot', 'bifid halluces']",,,295006,,,,,,,,,
mondo:0017460,syndactyly type 6,"['unilateral syndactyly of digits 2-5', 'mitten hand', 'syndactyly, mitten type']",,,295012,CN203203,,,,,,,,
mondo:0017461,familial isolated clinodactyly of fingers,,,,295014,,,,,,,,,
mondo:0017462,congenital pseudoarthrosis of the tibia,"['congenital pseudarthrosis of the tibia', 'congenital pseudarthrosis of tibia']",,,295018,C0265661,,C132080,,,,,,
mondo:0017463,congenital pseudoarthrosis of the femur,['congenital pseudarthrosis of the femur'],,,295020,,,,,,,,,
mondo:0017464,congenital pseudoarthrosis of the fibula,['congenital pseudarthrosis of the fibula'],,,295022,,,,,,,,,
mondo:0017465,congenital pseudoarthrosis of the radius,['congenital pseudarthrosis of the radius'],,,295024,,,,,,,,,
mondo:0017466,congenital pseudoarthrosis of the ulna,['congenital pseudarthrosis of the ulna'],,,295026,,,,,,,,,
mondo:0017467,tibio-fibular synostosis,['Tibio-fibular fusion'],,,295028,,,,,,,,,
mondo:0017468,congenital shoulder dislocation,,,,295030,,,,,,755.59,,,
mondo:0017469,congenital elbow dislocation,"['congenital radial head dislocation', 'isolated congenital radial head dislocation', 'isolated congenital elbow dislocation']",,,295032,,,,,,,,,
mondo:0017470,congenital knee dislocation,"['congenital knee dislocation', 'congenital knee dislocation (disease)']",,,295034,,,,,,754.41,,10010520,0005191
mondo:0017471,congenital patella dislocation,"['congenital patellar dislocation', 'congenital dislocation of the patella']",,,295036,,,,,C538081,,,,
mondo:0017472,"patella aplasia/hypoplasia, unilateral",,,,295038,,,,,,,,,
mondo:0017473,"patella aplasia/hypoplasia, bilateral",,,,295041,,,,,,,,,
mondo:0017474,macrodactyly of fingers,"['macrodactyly of the hand', 'macrodactyly of hand', 'Megalodactyly of the hand', 'megalodactylism of the hand']",,,295044,,,,,C537720,,,,0100746
mondo:0017475,macrodactyly of toes,"['macrodactyly of the foot', 'macrodactyly of foot', 'megalodactylism of the foot', 'Megalodactyly of the foot']",,,295047,,,,,C537719,,,,0100747
mondo:0017476,upper limb hypertrophy,,,,295049,,,,,,,,,
mondo:0017477,lower limb hypertrophy,,,,295051,,,,,,,,,
mondo:0017478,"amelia of upper limb, unilateral",,,,295053,,,,,,,,,
mondo:0017479,"amelia of upper limb, bilateral",,,,295055,,,,,,,,,
mondo:0017480,"amelia of lower limb, unilateral",,,,295057,,,,,,,,,
mondo:0017481,"amelia of lower limb, bilateral",,,,295059,,,,,,,,,
mondo:0017482,"humeral agenesis/hypoplasia, unilateral","['humeral intercalary meromelia, unilateral']",,,295061,,,,,,,,,
mondo:0017483,"humeral agenesis/hypoplasia, bilateral","['humeral intercalary meromelia, bilateral']",,,295063,,,,,,,,,
mondo:0017484,"femoral agenesis/hypoplasia, unilateral","['femoral intercalary meromelia, unilateral']",,,295065,,,,,,,,,
mondo:0017485,"femoral agenesis/hypoplasia, bilateral","['femoral intercalary meromelia, bilateral']",,,295067,,,,,,,,,
mondo:0017486,"radial hemimelia, unilateral","['radial longitidinal meromelia, unilateral']",,,295069,,,,,,,,,
mondo:0017487,"radial hemimelia, bilateral","['radial longitidinal meromelia, bilateral']",,,295071,,,,,,,,,
mondo:0017488,"ulnar hemimelia, bilateral","['ulnar longitudinal meromelia, bilateral']",,,295073,,,,,,,,,
mondo:0017489,"ulnar hemimelia, unilateral","['ulnar longitudinal meromelia, unilateral']",,,295075,,,,,,,,,
mondo:0017490,"tibial hemimelia, unilateral","['tibial longitudinal meromelia, unilateral']",,,295077,CN203228,,,,,,,,
mondo:0017491,"tibial hemimelia, bilateral","['tibial longitudinal meromelia, bilateral']",,,295079,CN203229,,,,,,,,
mondo:0017492,"fibular hemimelia, unilateral","['fibular longitudinal meromelia, unilateral']",,,295081,,,,,,,,,
mondo:0017493,"fibular hemimelia, bilateral","['fibular longitudinal meromelia, bilateral']",,,295083,,,,,,,,,
mondo:0017496,"congenital absence of thigh and lower leg with foot present, unilateral","['Femorotibiofibular intercalary transverse meromelia, unilateral']",,,295089,,,,,,,,,
mondo:0017497,"congenital absence of thigh and lower leg with foot present, bilateral","['Femorotibiofibular intercalary transverse meromelia, bilateral']",,,295091,,,,,,,Q72.13,,
mondo:0017498,"congenital absence of both forearm and hand, unilateral","['radio-ulnar terminal transverse meromelia, unilateral']",,,295093,,,,,,,,,
mondo:0017499,"congenital absence of both forearm and hand, bilateral","['radio-ulnar terminal transverse meromelia, bilateral']",,,295095,,,,,,,Q71.23,,
mondo:0017500,"congenital absence of both lower leg and foot, unilateral","['tibiofibular terminal transverse meromelia, unilateral']",,,295097,,,,,,,,,
mondo:0017501,"congenital absence of both lower leg and foot, bilateral","['tibiofibular terminal transverse meromelia, bilateral']",,,295099,,,,,,,Q72.23,,
mondo:0017502,"acheiria, unilateral","['congenital absence of hand, unilateral']",,,295101,,,,,,,,,
mondo:0017503,"acheiria, bilateral","['congenital absence of hand, bilateral']",,,295103,,,,,,,,,
mondo:0017504,"apodia, unilateral","['congenital absence of foot, unilateral']",,,295105,,,,,,,,,
mondo:0017505,"apodia, bilateral","['congenital absence of foot, bilateral']",,,295107,,,,,,,,,
mondo:0017506,"congenital absence/hypoplasia of thumb, unilateral","['thumb hypodactyly, unilateral', 'thumb oligodactyly, unilateral']",,,295110,,,,,,,,,
mondo:0017507,"congenital absence/hypoplasia of thumb, bilateral","['thumb oligodactyly, bilateral', 'thumb hypodactyly, bilateral']",,,295112,,,,,,,,,
mondo:0017508,"congenital absence/hypoplasia of fingers excluding thumb, bilateral","['digits 2-5 hypodactyly, bilateral', 'Adactyly of hand, bilateral', 'digits 2-5 oligodactyly, bilateral']",,,295114,,,,,,,,,
mondo:0017509,"adactyly of foot, unilateral","['congenital absence of toes, unilateral']",,,295116,,,,,,,,,
mondo:0017510,"adactyly of foot, bilateral","['congenital absence of toes, bilateral']",,,295118,,,,,,,,,
mondo:0017511,"split hand, unilateral",,,,295120,,,,,,,,,
mondo:0017512,"split hand, bilateral",,,,295122,,,,,,,,,
mondo:0017513,"split foot, unilateral",,,,295124,,,,,,,,,
mondo:0017514,"split foot, bilateral",,,,295126,,,,,,,Q72.73,,
mondo:0017515,"brachydactyly of fingers, unilateral","['short fingers, unilateral']",,,295128,,,,,,,,,
mondo:0017516,"brachydactyly of fingers, bilateral","['short fingers, bilateral']",,,295130,,,,,,,,,
mondo:0017517,"brachydactyly of toes, unilateral","['short toes, unilateral']",,,295132,,,,,,,,,
mondo:0017518,"brachydactyly of toes, bilateral","['short toes, bilateral']",,,295134,,,,,,,,,
mondo:0017519,"symbrachydactyly of hand and foot, unilateral",,,,295136,CN203252,,,,,,,,
mondo:0017520,"symbrachydactyly of hand and foot, bilateral",,,,295138,CN203253,,,,,,,,
mondo:0017521,"hyperphalangy, unilateral","['supernumerary phalanx, unilateral', 'supernumerary phalanges, unilateral', 'hyperphalangy in digits 2-5']",,,295140,,,,,,,,,
mondo:0017522,"hyperphalangy, bilateral","['supernumerary phalanx, bilateral', 'supernumerary phalanges, bilateral']",,,295142,,,,,,,,,
mondo:0017523,"polydactyly of a biphalangeal thumb, unilateral","['preaxial polydactyly type 1, unilateral']",,,295144,CN203254,,,,,,,,
mondo:0017524,"polydactyly of a biphalangeal thumb, bilateral","['preaxial polydactyly type 1, bilateral']",,,295146,CN203255,,,,,,,,
mondo:0017525,"polydactyly of a triphalangeal thumb, unilateral","['preaxial polydactyly type 2, unilateral', 'unilateral PPD2']",,,295148,CN203256,,,,,,,,
mondo:0017526,"polydactyly of a triphalangeal thumb, bilateral","['preaxial polydactyly type 2, bilateral', 'bilateral PPD2']",,,295150,CN203257,,,,,,,,
mondo:0017527,"polydactyly of an index finger, unilateral","['preaxial polydactyly type 3, unilateral']",,,295152,CN203258,,,,,,,,
mondo:0017528,"polydactyly of an index finger, bilateral","['preaxial polydactyly type 3, bilateral']",,,295154,CN203259,,,,,,,,
mondo:0017529,"polysyndactyly, unilateral","['preaxial polydactyly type 4, unilateral']",,,295159,CN203260,,,,,,,,
mondo:0017530,"polysyndactyly, bilateral","['preaxial polydactyly type 4, bilateral']",,,295161,CN203261,,,,,,,,
mondo:0017531,"postaxial polydactyly type A, unilateral",,,,295163,CN203262,,,,,,,,
mondo:0017532,"postaxial polydactyly type A, bilateral",,,,295165,CN203263,,,,,,,,
mondo:0017533,"postaxial polydactyly type B, unilateral",,,,295167,CN203264,,,,,,,,
mondo:0017534,"postaxial polydactyly type B, bilateral",,,,295169,CN203265,,,,,,,,
mondo:0017535,"central polydactyly of fingers, unilateral","['mesoaxial polydactyly of fingers, unilateral', 'mirror hand, unilateral']",,,295171,,,,,,,,,
mondo:0017536,"central polydactyly of fingers, bilateral","['mesoaxial polydactyly of fingers, bilateral', 'mirror hand, bilateral']",,,295173,,,,,,,,,
mondo:0017537,"Preaxial polydactyly of toes, unilateral","['bifid hallux, unilateral', 'bifid great toes, unilateral', 'bifid halluces, unilateral']",,,295175,,,,,,,,,
mondo:0017538,"Preaxial polydactyly of toes, bilateral","['bifid great toes, bilateral', 'bifid halluces, bilateral', 'bifid hallux, bilateral']",,,295177,,,,,,,,,
mondo:0017543,zygodactyly type 2,"['Zygodactyly, Lueken type', 'SD1b', 'SD1, Lueken type', 'syndactyly type 1b', 'syndactyly type 1, Lueken type']",,,295189,CN203275,,,,,,,,
mondo:0017544,zygodactyly type 3,"['SD1, Montagu type', 'SD1c', 'syndactyly type 1, Montagu type', 'syndactyly type 1c', 'Zygodactyly, Montagu type']",,,295191,CN203276,,,,,,,,
mondo:0017545,zygodactyly type 4,"['syndactyly type 1d', 'Zygodactyly, Castilla type', 'SD1d', 'syndactyly type 1, Castilla type', 'SD1, Castilla type']",,,295193,CN203277,,,,,,,,
mondo:0017546,"congenital vertical talus, unilateral",,,,295201,,,,,,,,,
mondo:0017547,"congenital vertical talus, bilateral",,,,295203,,,,,,,,,
mondo:0017548,"humero-radio-ulnar synostosis, unilateral","['humero-radio-ulnar fusion, unilateral']",,,295205,,,,,,,,,
mondo:0017549,"humero-radio-ulnar synostosis, bilateral","['humero-radio-ulnar fusion, bilateral']",,,295207,,,,,,,,,
mondo:0017550,"humero-radial synostosis, unilateral","['humero-radial fusion, unilateral']",,,295209,,,,,,,,,
mondo:0017551,"humero-radial synostosis, bilateral","['humero-radial fusion, bilateral']",,,295211,,,,,,,,,
mondo:0017552,"humero-ulnar synostosis, unilateral","['humero-ulnar fusion, unilateral']",,,295213,,,,,,,,,
mondo:0017553,"humero-ulnar synostosis, bilateral","['humero-ulnar fusion, bilateral']",,,295215,,,,,,,,,
mondo:0017554,"radio-ulnar synostosis, unilateral","['radio-ulnar fusion, unilateral']",,,295217,CN203290,,,,,,,,
mondo:0017555,"radio-ulnar synostosis, bilateral","['radio-ulnar fusion, bilateral']",,,295219,CN203291,,,,,,,,
mondo:0017556,"Madelung deformity, unilateral",,,,295221,,,,,,,,,
mondo:0017557,"Madelung deformity, bilateral",,,,295223,,,,,,,,,
mondo:0017558,"congenital elbow dislocation, unilateral",,,,295225,,,,,,,,,
mondo:0017559,"congenital elbow dislocation, bilateral",,,,295227,,,,,,,,,
mondo:0017560,congenital genu recurvatum,"['genu recurvatum', 'hyperextension of knee deformity', 'hyperextension deformity of knee']",,,295229,,,C103184,,,754.40,,,
mondo:0017561,congenital genu flexum,,,,295232,,,,,,,,,
mondo:0017562,"congenital patella dislocation, unilateral",,,,295234,,,,,,,,,
mondo:0017563,"congenital patella dislocation, bilateral",,,,295237,,,,,,,,,
mondo:0017564,"macrodactyly of fingers, unilateral","['macrodactyly of hand, unilateral']",,,295239,,,,,,,,,
mondo:0017565,"macrodactyly of fingers, bilateral","['macrodactyly of hand, bilateral']",,,295241,,,,,,,,,
mondo:0017566,"macrodactyly of toes, unilateral","['macrodactyly of foot, unilateral']",,,295243,,,,,,,,,
mondo:0017567,"macrodactyly of toes, bilateral","['macrodactyly of foot, bilateral']",,,295245,,,,,,,,,
mondo:0017568,Prata-Liberal-Goncalves syndrome,"['brachydactyly-scoliosis-carpal fusion syndrome', 'acrodysplasia scoliosis']",,,2956,CN203304,,,,,,,,
mondo:0017569,de Barsy syndrome,"['progeroid syndrome, de Barsy type', 'corneal clouding, cutis laxa and intellectual disability', 'corneal clouding, cutis laxa and mental retardation', 'cutis laxa-corneal clouding-intellectual disability syndrome', 'De Barsy syndrome', 'progeroid syndrome of de Barsy', 'autosomal recessive cutis laxa type III', 'progeroid syndrome, De Barsy type', 'cutis laxa growth deficiency syndrome']",0070143,,2962,,"['-0.8296', '0.2815', '0.4177', '-0.1876', '0.3394', '-0.8193', '-0.0824', '0.5693', '-0.8916', '-0.2969', '-0.09534', '-0.1625', '0.3823', '-0.0922', '-0.0864', '0.6597', '0.6934', '-0.2864', '0.1523', '-0.7363', '-0.1725', '-0.008026', '-0.4363', '-0.3364', '-0.2695', '0.21', '-0.851', '-0.10626', '0.481', '-0.2222', '0.1036', '0.0001338', '0.5503', '0.2446', '-0.0896', '-0.2734', '0.0344', '-0.3538', '-0.00753', '0.0009685', '0.4006', '-0.5786', '-0.249', '0.1271', '0.2194', '-0.3853', '0.03607', '0.6953', '-0.171', '-0.4993', '-0.296', '0.0966', '-0.03564', '0.298', '-0.2039', '-0.1705', '0.1493', '-0.1256', '-0.31', '-0.135', '0.3435', '-0.1407', '-0.4016', '-0.2494', '0.3826', '-0.347', '0.4802', '0.508', '-0.02701', '0.1667', '-0.6157', '0.265', '0.2482', '-0.1125', '-0.11786', '0.7046', '-0.4043', '-0.5938', '-0.197', '0.3047', '0.3508', '0.325', '-0.5586', '0.8823', '-0.01978', '0.2893', '-0.07153', '0.3176', '0.3052', '0.2546', '0.4104', '0.7773', '0.4028', '0.284', '0.4023', '0.1958', '0.506', '-0.713', '1.055', '0.265']",,,C535990,,,,
mondo:0017570,leukocyte adhesion deficiency,"['LAD', 'congenital leukocyte adherence deficiency']",6612,,2968,C0272187,"['-0.0944', '0.068', '0.02406', '-0.2332', '0.0371', '-0.4163', '0.289', '0.2499', '0.2372', '-0.3665', '-0.6406', '-0.1508', '0.1553', '0.1906', '-0.1298', '-0.1842', '-0.1328', '-0.1798', '-0.1616', '-0.536', '-0.2465', '0.1609', '0.9556', '-0.10956', '-0.05234', '-0.085', '-0.2668', '-0.1514', '-0.0554', '-0.299', '-0.2212', '0.527', '0.514', '-0.1054', '0.2495', '0.43', '-0.7554', '-0.636', '-0.4917', '0.1759', '0.2888', '-0.121', '0.178', '-0.3037', '-0.0809', '-0.00275', '-0.10144', '-0.4077', '-0.0643', '-0.2751', '0.5776', '-0.3289', '0.3792', '0.3518', '-0.07587', '-0.1815', '-0.05475', '0.356', '-0.3503', '0.574', '-0.4775', '0.436', '0.2032', '-0.2068', '0.5723', '-0.2178', '0.4353', '0.1361', '-0.793', '0.5166', '0.1048', '-0.454', '-0.3694', '-0.1708', '0.2471', '0.1808', '0.258', '0.1271', '0.005486', '0.142', '-0.1159', '0.183', '-0.495', '0.3184', '-0.2052', '-0.02039', '0.572', '0.4688', '0.551', '0.1764', '0.2556', '0.8066', '0.1704', '-0.0794', '0.756', '0.727', '0.4329', '-0.9434', '0.4685', '-0.1242']",C27874,,,,,,
mondo:0017571,Proteus-like syndrome,"['Cohen-Hayden syndrome', 'Proteus like syndrome mental retardation eye defect', 'Proteus like syndrome intellectual disability eye defect']",,,2969,,,C179930,,,,,,
mondo:0017572,tick-borne encephalitis,"['Far Eastern TBE', 'Western European tick-borne encephalitis', 'Russian spring-summer encephalitis', 'taiga encephalitis', 'west-Siberian encephalitis', 'Siberian tick-borne encephalitis', 'Tick-borne viral encephalitis', 'TBE', 'central European encephalitis']",0050175,,297,C0014061,,C34579,1001309,D004675,063.2,,10043848,
mondo:0017573,"46,XX disorder of sex development-anorectal anomalies syndrome",['female pseudohermaphroditism-anorectal anomalies syndrome'],,,2973,CN203326,,,,,,,,
mondo:0017574,chronic intestinal pseudoobstruction,"['intestinal pseudo-obstruction, chronic', 'cipo', 'chronic intestinal pseudo-obstruction']",,,2978,,"['-0.1942', '-0.2058', '0.05725', '-0.04507', '-0.10864', '-0.3765', '0.1354', '0.2576', '-0.412', '-0.1433', '-0.2421', '-0.478', '0.1674', '0.3208', '-0.2532', '0.1384', '0.07623', '0.134', '-0.8833', '-0.615', '0.1495', '-0.776', '0.648', '-0.158', '-0.1334', '0.09686', '0.03726', '0.487', '0.6304', '-0.0696', '0.5137', '-0.09015', '0.2842', '0.3057', '0.01935', '0.2856', '-0.2408', '-0.1819', '0.2913', '0.399', '-0.434', '-0.1498', '0.7744', '0.03766', '0.543', '-0.3352', '-0.509', '-0.4592', '-0.1449', '0.748', '-0.674', '-0.2297', '0.1022', '-0.3123', '-0.1602', '0.208', '-0.4592', '-0.2922', '-0.5234', '-0.07074', '0.4502', '0.43', '-0.1625', '0.00905', '0.1176', '0.1555', '0.6', '-0.0869', '0.2505', '0.5396', '-0.3767', '-0.373', '-0.1145', '0.0435', '0.064', '-0.05566', '0.5483', '0.336', '-0.05728', '-0.611', '-0.1709', '-0.47', '-0.4075', '0.4312', '-0.2622', '0.1399', '-0.08887', '0.3318', '0.6016', '-0.857', '-0.04877', '-0.3774', '-0.246', '0.03244', '0.3083', '-0.04453', '0.11334', '-0.3936', '0.4077', '0.3237']",,,,,,,
mondo:0017575,mitochondrial neurogastrointestinal encephalomyopathy,"['mitochondrial Neurogastrointestingal encephalopathy', 'myoneurogastrointestinal encephalopathy syndrome', 'oculogastrointestinal muscular dystrophy', 'OGIMD', 'thymidine phosphorylase deficiency', 'polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudo-obstruction', 'MNGIE syndrome', 'Mitochondrial neurogastrointestinal encephalopathy', 'mitochondrial neurogastrointestinal encephalopathy syndrome', 'POLIP', 'MNGIE']",,,298,,,C119678,,C537477,,,,
mondo:0017576,"46,XX disorder of sex development","['46,XX disorders of Sex development', '46,XX differences of Sex development', 'female pseudohermaphroditism', '46,XX DSD']",,,325697,CN776919,,C127169,,D058489,,,,
mondo:0017577,spontaneous periodic hypothermia,"['spontaneous periodic hypothermia syndrome', 'Shapiro^s syndrome', 'spontaneous recurrent hypothermia syndrome', 'episodic spontaneous hypothermia', 'Shapiro syndrome', 'recurrent spontaneous hypothermia with hypoplasia of the corpus callosum']",,,29822,C2931542,,,,C537594,,,,
mondo:0017578,disorder of thiamine metabolism and transport,,,,298644,CN227150,,,,,,,,
mondo:0017579,Baraitser-Winter cerebrofrontofacial syndrome,"['trigonocephaly ptosis coloboma', 'trigonocephaly ptosis mental retardation', 'iris coloboma with ptosis hypertelorism and mental retardation', 'cerebro-frontofacial syndrome, type 3', 'Baraitser-winter syndrome', 'Fryns-Aftimos syndrome', 'BRWS', 'iris coloboma with ptosis hypertelorism and intellectual disability', 'trigonocephaly ptosis intellectual disability']",0060229,,2995,,"['-0.07916', '0.3787', '-0.2161', '-0.4333', '-0.3186', '-0.3152', '0.8022', '0.7075', '-1.11', '-0.1411', '-0.1718', '0.0831', '0.563', '0.251', '-0.0804', '-0.4849', '0.533', '-0.902', '-0.2267', '-0.4883', '0.3232', '0.5693', '0.5093', '0.3022', '-0.02588', '-0.117', '-0.6704', '0.1384', '0.545', '0.415', '-0.3054', '-0.4368', '0.2651', '0.75', '0.288', '-0.6245', '-0.7046', '-0.5815', '-0.1244', '0.0436', '0.57', '-0.636', '-0.1958', '0.201', '0.3271', '0.01508', '0.3508', '0.2942', '0.11017', '-0.0585', '0.319', '-0.2435', '0.0926', '0.1968', '0.06195', '0.128', '0.2546', '-0.3484', '-0.227', '0.691', '0.2805', '-0.1803', '-0.6294', '0.02945', '-0.4585', '-0.0468', '0.4531', '0.2125', '-0.2913', '0.4004', '0.178', '0.4412', '0.1426', '0.1517', '-0.267', '-0.08527', '-0.0883', '-0.5537', '-0.02931', '-0.2314', '0.4338', '0.6426', '-0.3237', '0.709', '0.2444', '0.182', '-0.0925', '-0.2085', '0.2369', '0.7144', '0.1836', '0.3699', '0.3413', '0.3586', '0.2357', '-0.294', '0.2688', '-0.4282', '0.79', '0.3586']",,,,759.89,,,
mondo:0017580,11p15.4 microduplication syndrome,"['dup(11)p(15.4)', 'trisomy 11p15.4']",,,300305,CN203376,,,,,,,,
mondo:0017581,familial infantile gigantism,"['infantile gigantism due to pituitary hyperplasia', 'hereditary infantile gigantism', 'X-LAG (X-linked acrogigantism)', 'hereditary pituitary hyperplasia']",,,300373,CN203384,,,,,,,,
mondo:0017582,pituitary adenocarcinoma,"['carcinoma of pituitary gland', 'cancer of pituitary gland', 'cancer of pituitary', 'carcinoma of pituitary', 'pituitary carcinoma', 'pituitary gland carcinoma', 'cancer of the pituitary gland', 'pituitary gland cancer', 'carcinoma of the pituitary', 'PTCA', 'pituitary adenocarcinoma (disease)', 'cancer of the pituitary', 'carcinoma of the pituitary gland', 'pituitary gland adenocarcinoma']",4916,,300385,C0346300,,C4536,,,,,,0011763
mondo:0017583,mirror polydactyly-vertebral segmentation-limbs defects syndrome,,,,3004,CN203387,,,,,,,,
mondo:0017584,Sagliker syndrome,,,,300493,CN203388,,,,,,,,
mondo:0017585,painful orbital and systemic neurofibromas-marfanoid habitus syndrome,"['multiple orbital neurofibromas, painful peripheral nerve tumors, distinctive face and marfanoid habitus']",,,300501,CN203391,,,,,,,,
mondo:0017586,onychocytic matricoma,['acanthoma of the nail matrix'],,,300504,CN203392,,,,,,,,
mondo:0017587,onychomatricoma,"['nail matrix tumor', 'tumour of nail matrix', 'nail matrix tumour', 'tumor of nail matrix', 'neoplasm of nail matrix']",,,300512,CN203393,,,,,,,,
mondo:0017588,nail tumor,"['rare nail tumour', 'nail neoplasm (disease)', 'tumour of nail', 'rare nail tumor', 'neoplasm of nail', 'nail tumor', 'tumor of nail']",,,300515,,,,,,,,,
mondo:0017589,follicular cholangitis and pancreatitis,['follicular pancreatocholangitis'],,,300552,,,,,,,,,
mondo:0017590,carcinoma of the ampulla of vater,"['Ampulloma', 'ampullary cancer', 'ampulla of Vater carcinoma', 'ampullary carcinoma', 'ampulla of Vater cancer', 'carcinoma of ampulla of vater', 'hepatopancreatic ampulla carcinoma', 'AMPCA', 'carcinoma of hepatopancreatic ampulla']",4932,,300557,C0262401,,C3908,1000079,,,,10048853,
mondo:0017591,combined pulmonary fibrosis-emphysema syndrome,['CPFE'],,,300564,CN203401,,,,,,,,
mondo:0017592,staphylococcal toxemia,,,,300579,C0854511,,,,,,,10041932,
mondo:0017593,juvenile amyotrophic lateral sclerosis,"['amyotrophic lateral sclerosis, juvenile', 'juvenile Charcot disease', 'JALS', 'juvenile Lou Gehrig disease']",,,300605,CN239582,"['-0.0551', '0.2059', '0.2401', '0.09424', '-0.5273', '-0.814', '0.3867', '1.287', '-0.9233', '-0.3445', '0.1672', '0.319', '-0.0545', '0.003355', '1.116', '-0.2274', '0.0086', '0.1829', '-0.2559', '-0.5483', '0.2803', '-0.2656', '0.03674', '-0.1378', '-0.12415', '-0.11707', '-0.8345', '0.28', '-0.4316', '-0.0886', '0.921', '-0.0661', '0.1975', '-0.3376', '0.6445', '-0.3296', '-0.464', '0.11584', '-0.09033', '0.378', '0.08734', '-0.792', '-0.1796', '0.025', '0.674', '-0.2133', '-0.5815', '0.3486', '0.2625', '-0.0986', '-0.2744', '0.564', '-0.4463', '-0.1326', '-0.03638', '-0.4468', '0.2106', '-0.2646', '0.252', '0.695', '0.3', '-0.3018', '0.4', '-0.0692', '-0.3477', '-0.1249', '0.1722', '0.659', '-0.3562', '0.6353', '0.325', '-0.1664', '-0.0331', '0.352', '0.752', '0.355', '-0.562', '-0.00477', '-0.303', '-0.163', '0.06122', '-0.472', '0.3342', '0.7773', '0.0401', '0.4436', '0.1954', '0.3267', '0.8135', '0.07526', '0.2495', '-0.298', '-0.4377', '-0.1794', '0.341', '0.02643', '0.4893', '-0.0661', '0.189', '0.1519']",,,,,,,
mondo:0017594,indolent B-cell non-Hodgkin lymphoma,"['indolent B cell lymphoma', 'indolent B-cell NHL', 'B cell lymphoma, indolent']",,,300842,,,C171299,,,,,,
mondo:0017595,aggressive B-cell non-Hodgkin lymphoma,['aggressive B-cell NHL'],,,300846,,,C178541,,,,,,
mondo:0017596,diffuse large B-cell lymphoma of the central nervous system,"['CNS DLBCL', 'central nervous system diffuse large B-cell lymphoma', 'primary diffuse large B-cell lymphoma of the central nervous system', 'diffuse large B-cell lymphoma of central nervous system', 'primary DLBCL of the CNS', 'DLBCL of the CNS']",0081313,,300849,C2026186,,C71720,,,,,,
mondo:0017597,T-cell/histiocyte rich large B cell lymphoma,"['THRLBCL', 'T-cell rich/histiocyte-rich large B-cell lymphoma', 'T-cell/histiocyte-rich large B-cell lymphoma', 'T-cell/histiocyte rich lymphoma']",,,300857,C1321547,,C9496,,,,,,
mondo:0017598,primary cutaneous anaplastic large cell lymphoma,"['primary cutaneous CD30 Positive anaplastic large cell lymphoma', 'primary cutaneous CD30+ ALCL', 'primary anaplastic large cell lymphoma of skin', 'anaplastic large-cell lymphoma, primary cutaneous type', 'regressive atypical histiocytosis', 'primary cutaneous CD30+ anaplastic large cell lymphoma', 'C-ALCL', 'ALCL, cutaneous', 'primary anaplastic large cell lymphoma of the skin', 'primary C-ALCL']",,,300865,C1301362,,C6860,,D054446,,,10065863,
mondo:0017599,splenic diffuse red pulp small B-cell lymphoma,"['SDRPL', 'splenic diffuse red pulp lymphoma']",,,300869,C2699508,,C80309,,,,,,
mondo:0017600,hairy cell leukemia variant,"['HCL-v', 'prolymphocytic variant of hairy cell leukemia', 'prolymphocytic variant of HCL', 'hairy cell leukemia variant', 'leukemic reticuloendotheliosis variant', 'HCL-V', 'prolymphocytic variant of hairy cell leukaemia']",713,,300878,C0349633,,C7401,,,,,10019054,
mondo:0017601,diffuse large B-cell lymphoma with chronic inflammation,['DLBCL with chronic inflammation'],,,300888,,,,,,,,,
mondo:0017602,ALK-positive anaplastic large cell lymphoma,"['ALK-positive anaplastic large cell lymphoma', 'ALK+ ALCL', 'anaplastic large cell lymphoma, ALK-positive', 'ALK+ anaplastic large cell lymphoma', 'ALCL, ALK+', 'ALKoma']",,,300895,C1332079,,C37193,,,,,,
mondo:0017603,ALK-negative anaplastic large cell lymphoma,"['ALCL, ALK-', 'ALK- anaplastic large cell lymphoma', 'ALK- ALCL', 'ALK-negative anaplastic large cell lymphoma', 'anaplastic large cell lymphoma, ALK-negative']",,,300903,C1332078,,C37194,1000083,,,,,
mondo:0017604,marginal zone lymphoma,"['lymphoma of marginal zone B cell', 'MZBCL', 'marginal zone B-cell lymphoma', 'marginal zone B cell lymphoma', 'marginal zone lymphoma', 'MZL']",0050748,,300912,C1367654,,C4341,1000630,,,,,
mondo:0017607,caudal regression sequence,"['sacral agenesis syndrome', 'caudal dysplasia', 'sacral regression syndrome']",0080700,,3027,C1867774,"['0.276', '0.2612', '-0.10504', '-0.661', '-0.0601', '0.24', '0.3687', '0.5723', '-1.018', '-0.136', '-0.7676', '-0.654', '-0.2803', '0.4543', '-0.2064', '0.4712', '-0.2145', '-0.282', '0.0315', '-0.8203', '0.05698', '0.3162', '0.781', '-0.0788', '-0.0618', '-0.0694', '0.442', '0.593', '0.2448', '0.0121', '0.3726', '-0.423', '-0.1278', '-0.2947', '-0.1404', '0.00886', '0.4983', '-0.6963', '0.405', '-0.1497', '-0.339', '-0.05237', '-0.1936', '-0.07556', '0.4448', '-0.01045', '0.2308', '0.01542', '-0.03665', '0.4038', '-0.3623', '0.3394', '0.2627', '-0.7344', '-1.174', '-0.07025', '0.1617', '-0.2299', '-0.3064', '0.00895', '-0.2239', '0.05194', '0.0947', '0.2205', '0.1776', '0.0686', '0.04623', '-0.0668', '-0.698', '0.2024', '0.02737', '-0.03815', '-0.4932', '-0.3474', '0.02559', '0.1073', '0.4595', '0.04596', '-0.1732', '-0.3406', '-0.7314', '-0.00712', '0.4087', '0.568', '-0.1583', '0.1729', '-0.1372', '0.02136', '-0.06', '-0.1946', '-0.299', '0.5483', '-0.2505', '0.369', '0.5234', '-0.285', '0.6777', '-0.03607', '0.1082', '0.549']",C124505,,,,,10068896,
mondo:0017609,renal tubular dysgenesis,"['renotubular dysgenesis', 'primitive renal tubule syndrome']",,,3033,,,,,,,,,
mondo:0017610,epidermolysis bullosa simplex,"['EEB', 'epidermolysis bullosa intraepidermic', 'EBS', 'epidermolysis bullosa simplex']",4644,,304,C0079298,"['0.917', '-0.1724', '-0.4587', '-0.00879', '-0.035', '-0.6665', '-0.5483', '0.4136', '-0.03035', '-0.681', '0.1781', '-0.418', '-0.8965', '0.5103', '-0.54', '0.1681', '0.1621', '-1.189', '-0.3083', '-0.874', '-0.4612', '-0.376', '0.49', '0.7573', '0.0781', '0.4167', '-0.9673', '0.7236', '-0.1654', '-0.6553', '0.2267', '0.00786', '-0.216', '0.11676', '0.2074', '0.1392', '-1.047', '0.0372', '0.8945', '-0.728', '0.127', '-0.527', '0.1605', '-0.1715', '0.2805', '-0.2798', '-0.4644', '0.1522', '0.4436', '0.1488', '-0.3872', '-0.9463', '0.6567', '-0.06885', '-0.1359', '-0.502', '-0.2332', '1.247', '-0.7944', '-0.4224', '-0.2546', '0.1725', '0.323', '0.1967', '0.752', '0.779', '0.457', '0.2045', '-0.3801', '0.1849', '-0.01735', '-0.00583', '-0.4082', '-0.1642', '0.1492', '-0.04526', '0.03586', '-0.03029', '0.072', '-0.3215', '-1.034', '0.05246', '-0.524', '-0.2235', '0.1217', '0.1365', '-0.8223', '0.8438', '0.9727', '0.2474', '-0.4724', '0.282', '0.1144', '0.721', '-0.1571', '0.7026', '0.308', '-0.4458', '0.7827', '0.2979']",C84692,,D016110,757.39,Q81.0,,
mondo:0017611,pituitary tumor,"['tumour of pituitary gland', 'pituitary gland tumor', 'tumour of the pituitary', 'tumour of the pituitary gland', 'pituitary gland neoplasm', 'neoplasm of pituitary gland', 'tumor of the pituitary gland', 'neoplasm of the pituitary', 'pituitary tumor', 'pituitary gland tumour', 'tumor of the pituitary', 'tumour of pituitary', 'pituitary neoplasm', 'neoplasm of pituitary', 'tumor of pituitary', 'tumor of pituitary gland', 'neoplasm of the pituitary gland']",,,304055,C0032019,,C3330,,,239.7,,,
mondo:0017612,junctional epidermolysis bullosa,"['EBJ', 'JEB', 'epidermolysis bullosa, junctional', 'epidermolysis bullosa atrophicans']",3209,,305,C0079301,,C90598,,D016109,,,,
mondo:0017613,intellectual disability-hypotonia-skin hyperpigmentation syndrome,"['Medrano-Roldan syndrome', 'Medrano Roldan syndrome']",,,3050,,,,,,,,,
mondo:0017614,X-linked intellectual disability-hypogonadism-ichthyosis-obesity-short stature syndrome,"['Sex-linked mental retardation, short stature, obesity and hypogonadism', 'X-linked intellectual disability - short stature – obesity', 'Sex-linked intellectual disability, short stature, obesity and hypogonadism', 'Young-Hughes syndrome']",,,3055,C0796264,,,,C536715,,,,
mondo:0017615,benign familial infantile epilepsy,"['seizures, benign familial infantile', 'BFIC', 'benign familial infantile convulsions', 'benign familial infantile seizures', 'BFIS', 'BFIE', 'benign familial infantile convulsion']",0060169,,306,CN203492,"['0.868', '0.1494', '-0.2686', '-0.03857', '-0.5464', '-0.5786', '0.803', '0.4465', '-0.4854', '-0.4722', '-0.01814', '-0.3108', '-0.253', '0.5', '-0.1602', '0.0248', '-0.352', '-0.6357', '-0.2913', '-0.525', '-0.05222', '0.4631', '0.1842', '-0.512', '-0.1633', '0.0708', '-0.1833', '-0.2277', '-0.4302', '0.3315', '0.4312', '-0.709', '0.1715', '0.2476', '0.7437', '0.346', '-0.02884', '0.03348', '-0.0894', '-0.27', '0.099', '-0.3074', '0.1477', '-0.369', '-0.5786', '-0.519', '-0.1678', '0.2659', '0.2346', '0.6475', '-0.04535', '0.0809', '0.04483', '-0.5547', '0.1254', '-0.0846', '-0.1354', '0.04294', '-0.2656', '0.3303', '-0.6772', '0.4607', '0.594', '-0.3672', '-0.1816', '1.224', '0.1288', '-0.1348', '-0.7607', '0.7407', '1.078', '1.091', '-0.09674', '-0.4204', '0.10333', '0.7544', '0.9995', '0.3682', '-0.5117', '0.3179', '0.1151', '0.844', '0.4136', '0.032', '0.4543', '0.2117', '0.2832', '0.633', '0.748', '0.4377', '0.1942', '0.0452', '-0.2852', '0.01613', '0.2322', '0.1906', '0.3623', '-0.643', '0.3064', '0.2664']",,,,V17.2,,,
mondo:0017616,"X-linked intellectual disability, Schutz type",,,,3062,,,,,,,,,
mondo:0017617,acquired adult-onset immunodeficiency,"['acquired immunodeficiency of adults', 'adult-onset immunodeficiency with anti-interferon-gamma autoantibodies', 'adult-onset immunodeficiency due to anti-interferon-gamma autoantibody', 'anti-IFN-gamma autoantibody syndrome', 'adult-onset immunodeficiency with acquired Anti-interferon-gamma autoantibodies', 'adult onset immunodeficiency syndrome']",,,306431,,,,,,,,,
mondo:0017618,congenital sucrase-isomaltase deficiency with starch intolerance,"['CSID with starch intolerance', 'congenital sucrose intolerance with starch intolerance', 'congenital sucrase-isomaltose malabsorption with starch intolerance', 'disaccharide intolerance with starch intolerance']",,,306436,,,,,,,,,
mondo:0017619,congenital sucrase-isomaltase deficiency with minimal starch tolerance,"['CSID with minimal starch tolerance', 'congenital sucrose intolerance with minimal starch tolerance', 'disaccharide intolerance with minimal starch tolerance', 'congenital sucrase-isomaltose malabsorption with minimal starch tolerance']",,,306446,,,,,,,,,
mondo:0017620,congenital sucrase-isomaltase deficiency without starch intolerance,"['congenital sucrose intolerance without starch intolerance', 'CSID without starch intolerance', 'congenital sucrase-isomaltose malabsorption without starch intolerance', 'disaccharide intolerance without starch intolerance']",,,306462,,,,,,,,,
mondo:0017621,congenital sucrase-isomaltase deficiency with starch and lactose intolerance,"['disaccharide intolerance with starch and lactose intolerance', 'congenital sucrase-isomaltose malabsorption with starch and lactose intolerance', 'congenital sucrose intolerance with starch and lactose intolerance', 'CSID with starch and lactose intolerance']",,,306474,,,,,,,,,
mondo:0017622,congenital sucrase-isomaltase deficiency without sucrose intolerance,"['congenital sucrose-isomaltose malabsorption without sucrose intolerance', 'CSID without sucrose intolerance', 'disaccharide intolerance without sucrose intolerance']",,,306486,,,,,,,,,
mondo:0017623,PTEN hamartoma tumor syndrome,['PHTS'],0080191,,306498,C1959582,,C179915,,,,,,
mondo:0017624,familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis,"['Michellis-Castrillo syndrome', 'FHHNC']",,,306516,CN203511,,,,,,,,
mondo:0017625,familial primary hypomagnesemia with hypocalcuria,,,,306519,CN227163,,,,,,,,
mondo:0017626,familial primary hypomagnesemia with normocalcuria,,,,306522,CN227164,,,,,,,,
mondo:0017627,congenital hereditary facial paralysis-variable hearing loss syndrome,"['congenital hereditary facial paralysis-variable deafness syndrome', 'congenital hereditary facial paralysis with variable deafness', 'congenital hereditary facial palsy with variable deafness', 'congenital hereditary facial palsy with variable hearing loss']",,,306530,,"['0.709', '0.1517', '0.5034', '0.4805', '-0.7197', '0.1979', '1.005', '0.792', '-0.1393', '-0.8037', '0.4558', '0.283', '-0.3237', '0.323', '-0.4832', '-0.4968', '-0.65', '0.09814', '-0.5503', '-0.3047', '0.1648', '0.2281', '-0.7417', '0.5547', '0.969', '0.2585', '-0.9673', '-0.10345', '-0.4548', '-0.2496', '-0.05945', '-0.0786', '0.4922', '-0.1527', '-0.5874', '-0.2201', '-0.369', '-0.629', '-0.03217', '-0.7935', '0.2059', '-0.1975', '-0.10046', '-0.3157', '0.2439', '-0.793', '0.0582', '0.3564', '0.11194', '-0.10535', '0.02397', '-0.5044', '-0.3428', '-0.1342', '0.3071', '0.521', '-0.1841', '0.2368', '-0.275', '0.5825', '-0.05737', '0.93', '-0.484', '0.2001', '-0.5786', '0.0671', '-0.4756', '0.8066', '-0.509', '-0.2544', '-0.04532', '0.934', '1.16', '-0.964', '0.5103', '-0.10016', '1.049', '0.2886', '0.07227', '-0.0497', '0.1074', '-0.8643', '-0.574', '0.994', '0.1648', '-0.211', '-0.2179', '1.501', '-0.0324', '0.6987', '0.3953', '0.3162', '-0.0587', '0.623', '0.496', '0.1289', '-0.268', '-1.257', '-0.199', '-0.03537']",,,,,,,
mondo:0017628,myospherulosis,"['spherulocytosis', 'subcutaneous spherulocystic disease']",,,306553,C0027123,,,,,136.8,,,
mondo:0017629,sodium channelopathy-related small fiber neuropathy,,,,306577,,"['-0.5005', '-0.1285', '0.3557', '0.002464', '-0.1997', '0.1813', '-0.07855', '0.5713', '-0.252', '0.3206', '-0.1318', '0.058', '0.0455', '0.01367', '-0.1088', '0.1527', '0.088', '-0.04495', '-0.1212', '-0.5244', '0.396', '-0.1181', '-0.112', '0.6943', '0.1051', '0.0396', '-0.1111', '0.0833', '-0.05444', '-0.4043', '0.101', '0.05145', '0.2382', '-0.01588', '-0.003382', '-0.3384', '0.2131', '-0.1157', '0.1665', '-0.7935', '0.012825', '-0.5474', '-0.06335', '0.2355', '-0.2764', '-0.3696', '-0.04373', '0.2583', '0.1311', '0.3367', '-0.3152', '0.3357', '0.02309', '0.00873', '-0.1202', '0.1775', '0.5117', '-0.1091', '-0.2856', '-0.1433', '-0.157', '0.2666', '-0.02518', '0.0633', '-0.3728', '0.006496', '0.0621', '0.4849', '0.205', '0.4268', '-0.2493', '0.102', '0.03574', '-0.0858', '0.414', '0.1338', '0.2217', '0.322', '-0.02597', '-0.08136', '0.1475', '-0.502', '0.4314', '0.4377', '-0.2737', '0.05594', '-0.1726', '0.2368', '0.285', '-0.1415', '0.04782', '-0.05', '-0.002304', '0.11584', '0.3828', '0.11', '0.147', '-0.2915', '-0.4705', '0.581']",,,,,,,
mondo:0017630,X-linked complicated spastic paraplegia type 1,['SPG1'],,,306617,CN203524,,,,,,,,
mondo:0017634,non-infectious anterior uveitis,['non-infectious iridocyclitis'],,,306648,C0339317,,,,,,,,
mondo:0017636,hemiparkinsonism-hemiatrophy syndrome,['Hp-HA syndrome'],,,306669,CN203531,,,,,,,,
mondo:0017638,manganese poisoning,"['manganese intoxication', 'Manganism']",,,306682,,,,1001808,D020149,503,,10058951,
mondo:0017639,carbon monoxide-induced parkinsonism,['CO-induced parkinsonism'],,,306686,C0393565,,,,,,,,
mondo:0017640,cyanide-induced parkinsonism,,,,306692,CN203536,,,,,,,,
mondo:0017642,intellectual disability-microcephaly-phalangeal-facial abnormalities syndrome,,,,3067,CN227166,,,,,,,,
mondo:0017648,Sydenham chorea,,,,306731,,,C168445,,,,,10042732,
mondo:0017649,hemidystonia-hemiatrophy syndrome,['HD-HA syndrome'],,,306741,CN203542,,,,,,,,
mondo:0017651,primary myoclonus,,,,306750,,,,,,,,,
mondo:0017656,motor stereotypies,,,,306765,,,,,,,,,
mondo:0017658,hyperekplexia,,,,306773,,,,,D000071017,,,,
mondo:0017659,sporadic hyperekplexia,,,,306776,,,,,,,,,
mondo:0017666,diffuse palmoplantar keratoderma,"['diffuse palmoplantar hyperkeratosis', 'diffuse keratosis palmoplantaris', 'diffuse PPK']",,,307141,C0022584,,,,,757.39,,,0007435
mondo:0017667,isolated diffuse palmoplantar keratoderma,"['nonsyndromic diffuse palmoplantar keratoderma', 'isolated diffuse PPK', 'isolated diffuse palmoplantar hyperkeratosis', 'isolated diffuse keratosis palmoplantaris']",,,307148,,,,,,,,,
mondo:0017668,intellectual disability-short stature-hypertelorism syndrome,"['intellectual deficit - short stature - hypertelorism', 'Stoll-Géraudel-Chauvin syndrome', 'intellectual disability short stature hypertelorism', 'mental retardation short stature hypertelorism', 'Stoll-GC)raudel-Chauvin syndrome']",,,3074,CN203552,,,,,,,,
mondo:0017670,autosomal dominant diffuse mutilating palmoplantar keratoderma,['autosomal dominant diffuse mutilating palmoplantar hyperkeratosis'],,,307773,CN229100,,,,,,,,
mondo:0017672,focal palmoplantar keratoderma,"['focal PPK', 'focal palmoplantar hyperkeratosis', 'focal keratosis palmoplantaris']",,,307837,,"['-0.00733', '0.141', '0.03745', '-0.03052', '0.02588', '-0.1282', '-0.01328', '0.0561', '-0.04004', '-0.03693', '-0.067', '-0.04022', '-0.04507', '-0.03047', '-0.02464', '0.006863', '0.04388', '-0.1631', '0.01131', '-0.2537', '-0.05963', '0.02481', '0.1108', '-0.00226', '0.06805', '-0.0202', '-0.04785', '0.03104', '-0.03723', '-0.0469', '0.09247', '-0.0378', '0.0808', '-0.00759', '0.02432', '0.010155', '-0.01177', '-0.0415', '-0.00842', '-0.0759', '0.01473', '-0.10565', '-0.004894', '-0.01598', '0.02187', '-0.05664', '-0.07513', '0.10645', '-0.0008807', '-0.03156', '-0.05655', '0.02554', '0.0928', '0.0776', '-0.02922', '-0.0621', '0.15', '-0.05276', '-0.1805', '-0.05194', '0.07153', '0.00618', '-0.03912', '-0.05603', '-0.00997', '0.05914', '0.1527', '0.07086', '-0.04538', '0.1498', '-0.1265', '-0.0327', '0.07587', '-0.02147', '0.0669', '0.0192', '0.03308', '0.005413', '-0.02061', '-0.08', '-0.02467', '0.06244', '0.02666', '0.0443', '0.04813', '-0.03976', '-0.00771', '0.12024', '0.1609', '0.091', '0.03625', '0.0901', '0.0412', '0.07043', '0.1682', '0.01659', '0.1042', '-0.11926', '0.0197', '0.01863']",,,,,,,
mondo:0017673,isolated focal palmoplantar keratoderma,"['nonsyndromic focal palmoplantar keratoderma', 'isolated focal PPK', 'isolated focal palmoplantar hyperkeratosis', 'isolated focal keratosis palmoplantaris']",,,307846,,,,,,,,,
mondo:0017675,punctate palmoplantar keratoderma,"['punctate PPK', 'punctate palmoplantar hyperkeratosis', 'punctate keratosis palmoplantaris']",0060361,,307967,C4024851,,,,,,,,
mondo:0017676,marginal papular palmoplantar keratoderma,['marginal papular palmoplantar hyperkeratosis'],,,307995,,,,,,,,,
mondo:0017677,focal acral hyperkeratosis,"['PPKP3 without elastoidosis', 'PPPK3 without elastoidosis', 'punctate palmoplantar hyperkeratosis type 3 without elastoidosis', 'punctate palmoplantar keratoderma type 3 without elastoidosis']",,,308013,C1302839,,,,,,,,
mondo:0017681,erythrokeratoderma variabilis progressiva,,,,308166,,,,,,,,,
mondo:0017682,intellectual disability-polydactyly-uncombable hair syndrome,"['mental retardation, postaxial polydactyly, phalangeal hypoplasia, 2-3 toe syndactyly, unusual face, uncombable hair', 'Kozlowski-Krajewska syndrome', 'intellectual disability, postaxial polydactyly, phalangeal hypoplasia, 2-3 toe syndactyly, unusual face, uncombable hair']",,,3082,C2931547,,,,C537615,,,,
mondo:0017683,methylcobalamin deficiency type cblDv1,['functional methionine synthase deficiency type cblDv1'],,,308380,CN203574,,,,,,,,
mondo:0017684,disorder of beta and omega amino acid metabolism,,,,308407,C0342707,,,,,270.8,,,
mondo:0017685,"vitamin B12-responsive methylmalonic acidemia, type cblDv2","['vitamin B12-responsive methylmalonic aciduria, type cblDv2']",,,308442,CN203582,,,,,,,,
mondo:0017686,inborn aminoacylase deficiency,"['aminoacylase deficiency', 'rare inborn error of aminoacylase activity', 'inborn error of aminoacylase activity']",,,308448,,,,,,,,,
mondo:0017687,disorder of neutral amino acid transport,"['inborn error of neutral amino acid transport', 'rare inborn error of neutral amino acid transport']",,,308451,CN203583,,,,,,,,
mondo:0017688,disorder of glycolysis,,,,308459,CN227176,,,,,,,,
mondo:0017689,disorder of fructose metabolism,,,,308463,C0342744,,,,,,,,
mondo:0017690,disorder of galactose metabolism,,,,308467,C0342745,,,,,,,,
mondo:0017691,erythrocyte galactose epimerase deficiency,"['erythrocyte uridine diphosphate galactose-4-epimerase deficiency', 'erythrocyte GALE-D', 'erythrocyte UDP-galactose-4-epimerase deficiency', 'erythrocyte GALE deficiency', 'erythrocyte epimerase deficiency galactosemia']",,,308473,C0574090,,,,,,,,
mondo:0017692,generalized galactose epimerase deficiency,"['generalised uridine diphosphate galactose-4-epimerase deficiency', 'generalized GALE deficiency', 'generalised UDP-galactose-4-epimerase deficiency', 'generalised GALE deficiency', 'generalized UDP-galactose-4-epimerase deficiency', 'generalised epimerase deficiency galactosemia', 'generalized epimerase deficiency galactosemia', 'generalized GALE-D', 'generalised GALE-D', 'generalized uridine diphosphate galactose-4-epimerase deficiency']",,,308487,C0574089,,,,,,,,
mondo:0017694,"glycogen storage disease due to acid maltase deficiency, infantile onset","['glycogen storage disease type II, infantile onset', 'glycogen storage disease type 2, infantile onset', 'Pompe disease, infantile onset', 'GSD type II, infantile onset', 'glycogenosis due to acid maltase deficiency, infantile onset', 'alpha-1,4-glucosidase acid deficiency, infantile onset', 'GSD type 2, infantile onset', 'glycogenosis type II, infantile onset', 'glycogenosis type 2, infantile onset', 'GSD due to acid maltase deficiency, infantile onset']",,,308552,CN203590,,,,,,,,
mondo:0017695,"glycogen storage disease due to glycogen branching enzyme deficiency, progressive hepatic form","['GBE deficiency, progressive hepatic form', 'glycogen storage disease type IV, progressive hepatic form', 'glycogenosis type IV, progressive hepatic form', 'GSD type 4, progressive hepatic form', 'glycogen storage disease type 4, progressive hepatic form', 'glycogenosis due to glycogen branching enzyme deficiency, progressive hepatic form', 'glycogenosis type 4, progressive hepatic form', 'GSDIV, progressive hepatic form', 'GSD due to glycogen branching enzyme deficiency, progressive hepatic form']",,,308621,CN203594,"['-0.04333', '0.1538', '-0.1309', '0.03123', '0.2098', '-0.2776', '0.05984', '0.2505', '-0.371', '-0.01026', '-0.01659', '-0.2155', '-0.06158', '0.0769', '-0.378', '-0.1267', '-0.1416', '-0.1055', '-0.4685', '-0.2416', '0.2932', '-0.05798', '0.4893', '0.01173', '-0.1572', '0.00942', '0.0814', '-0.2175', '-0.0876', '0.1853', '0.3079', '0.01312', '0.1405', '0.1455', '0.0752', '-0.2401', '-0.11334', '-0.06433', '-0.1731', '-0.2367', '-0.03085', '-0.5137', '0.02675', '0.3794', '-0.413', '-0.0693', '-0.01394', '0.07776', '-0.1558', '0.3896', '-0.0259', '0.02132', '0.1063', '0.0329', '-0.08923', '-0.4482', '0.2306', '0.01477', '-0.439', '-0.0068', '0.4172', '-0.1403', '0.245', '0.0613', '-0.2659', '0.04837', '0.1428', '0.1919', '-0.2788', '0.1214', '-0.286', '-0.1091', '0.0931', '0.2277', '0.2483', '0.307', '0.1431', '0.2007', '-0.3948', '-0.09576', '-0.131', '-0.07513', '-0.1201', '-0.05276', '-0.00905', '0.1779', '0.1323', '0.0872', '0.412', '-0.11914', '0.44', '0.02307', '-0.0721', '0.0055', '0.523', '0.3608', '0.2913', '-0.4155', '0.1082', '0.269']",,,,,,,
mondo:0017696,"glycogen storage disease due to glycogen branching enzyme deficiency, non progressive hepatic form","['GSDIV, non progressive hepatic form', 'glycogenosis due to glycogen branching enzyme deficiency, non progressive hepatic form', 'glycogen storage disease type IV, non progressive hepatic form', 'glycogenosis type 4, non progressive hepatic form', 'GSD type 4, non progressive hepatic form', 'glycogen storage disease type 4, non progressive hepatic form', 'GBE deficiency, non progressive hepatic form', 'glycogenosis type IV, non progressive hepatic form', 'GSD due to glycogen branching enzyme deficiency, non progressive hepatic form']",,,308638,CN203595,"['-0.04492', '0.184', '-0.1257', '0.006927', '0.2073', '-0.315', '0.0783', '0.2515', '-0.3577', '0.000495', '0.0002747', '-0.224', '-0.06836', '0.10034', '-0.411', '-0.10864', '-0.1329', '-0.0876', '-0.4895', '-0.2495', '0.3193', '-0.10046', '0.527', '-0.0321', '-0.2246', '0.003662', '0.123', '-0.2063', '-0.10895', '0.1766', '0.275', '0.08136', '0.2051', '0.1741', '0.0695', '-0.255', '-0.12', '-0.05743', '-0.1945', '-0.2255', '-0.00422', '-0.492', '0.05347', '0.348', '-0.42', '-0.05762', '-0.01202', '0.0634', '-0.172', '0.3865', '-0.00778', '0.04446', '0.1284', '0.066', '-0.0881', '-0.4612', '0.2155', '-0.003004', '-0.4292', '0.0007963', '0.4182', '-0.12146', '0.2717', '0.0732', '-0.2467', '0.04214', '0.1503', '0.1733', '-0.297', '0.1414', '-0.3328', '-0.08685', '0.09625', '0.1976', '0.258', '0.2866', '0.1721', '0.141', '-0.3894', '-0.08685', '-0.1339', '-0.0773', '-0.1475', '-0.06146', '0.02005', '0.1533', '0.1444', '0.08777', '0.3997', '-0.1481', '0.438', '0.02348', '-0.0948', '-0.0201', '0.509', '0.3584', '0.2583', '-0.3965', '0.1289', '0.2947']",,,,,,,
mondo:0017697,"glycogen storage disease due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form","['glycogen storage disease type 4, fatal perinatal neuromuscular form', 'GSDIV, fatal perinatal neuromuscular form', 'GSD type 4, fatal perinatal neuromuscular form', 'glycogenosis type 4, fatal perinatal neuromuscular form', 'glycogenosis type IV, fatal perinatal neuromuscular form', 'GSD due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form', 'GBE deficiency, fatal perinatal neuromuscular form', 'glycogen storage disease type IV, fatal perinatal neuromuscular form', 'glycogenosis due to glycogen branching enzyme deficiency, fatal perinatal neuromuscular form']",,,308655,C1856303,"['-0.4448', '0.1415', '-0.02484', '0.1971', '0.4348', '-0.2507', '-0.1755', '0.1724', '-0.1578', '0.0772', '-0.00536', '-0.09717', '-0.01401', '0.1283', '-0.1857', '-0.2515', '-0.1962', '-0.1609', '-0.4568', '-0.3687', '0.2263', '-0.1263', '0.5405', '-0.1348', '-0.1512', '-0.3477', '0.11487', '-0.1222', '-0.0265', '0.009995', '0.2217', '0.1664', '0.1598', '0.2122', '-0.08826', '-0.1923', '-0.08057', '0.1748', '-0.0691', '-0.2986', '0.0784', '-0.2842', '0.0896', '0.1512', '-0.3733', '-0.1384', '0.00609', '0.1531', '0.003868', '0.3145', '0.09296', '-0.3062', '0.391', '-0.08496', '-0.1555', '-0.5737', '0.404', '0.0743', '-0.4224', '0.02766', '0.1522', '-0.033', '0.3535', '-0.0384', '-0.2358', '0.1844', '0.2551', '0.01191', '-0.4482', '-0.01602', '-0.2998', '-0.02333', '0.067', '0.07135', '0.05582', '0.1587', '0.2461', '0.2473', '-0.4363', '-0.1072', '-0.3682', '0.00651', '-0.0694', '-0.007153', '0.1681', '0.1087', '0.3335', '0.1478', '0.2588', '0.0922', '0.0871', '0.266', '0.03494', '-0.05853', '0.4836', '0.3694', '0.3389', '-0.318', '-0.08136', '0.2014']",,,,,,,
mondo:0017698,"glycogen storage disease due to glycogen branching enzyme deficiency, congenital neuromuscular form","['glycogenosis type IV, congenital neuromuscular form', 'GSDIV, congenital neuromuscular form', 'GSD due to glycogen branching enzyme deficiency, congenital neuromuscular form', 'glycogenosis due to glycogen branching enzyme deficiency, congenital neuromuscular form', 'glycogen storage disease type IV, congenital neuromuscular form', 'GBE deficiency, congenital neuromuscular form', 'glycogen storage disease type 4, congenital neuromuscular form', 'glycogenosis type 4, congenital neuromuscular form', 'GSD type 4, congenital neuromuscular form']",,,308670,C1856304,"['-0.4158', '0.1244', '0.000393', '0.2074', '0.4543', '-0.225', '-0.1849', '0.1743', '-0.1633', '0.0783', '0.0092', '-0.0861', '-0.00546', '0.154', '-0.1876', '-0.2803', '-0.163', '-0.2096', '-0.4583', '-0.3599', '0.228', '-0.0949', '0.4326', '-0.0638', '-0.1279', '-0.3625', '0.06805', '-0.1761', '-0.0469', '0.00688', '0.2092', '0.1277', '0.135', '0.1766', '-0.0635', '-0.2024', '-0.1059', '0.2224', '-0.07837', '-0.3394', '0.0985', '-0.2766', '0.0739', '0.1752', '-0.3308', '-0.12006', '0.02663', '0.1886', '0.0356', '0.2986', '0.0526', '-0.2583', '0.3625', '-0.11096', '-0.152', '-0.551', '0.3984', '0.0907', '-0.5103', '-0.02089', '0.1736', '-0.02846', '0.3315', '-0.05542', '-0.2761', '0.1647', '0.268', '0.02847', '-0.4363', '-0.116', '-0.3215', '-0.00959', '0.0977', '0.05502', '0.11115', '0.2014', '0.252', '0.2346', '-0.478', '-0.0943', '-0.3171', '-0.006966', '-0.0665', '0.05093', '0.1276', '0.129', '0.3054', '0.1493', '0.2395', '0.0927', '0.11176', '0.2961', '0.0607', '-0.0541', '0.5273', '0.3274', '0.2993', '-0.3145', '-0.1181', '0.2573']",,,,,,,
mondo:0017699,"glycogen storage disease due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form","['glycogenosis due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form', 'glycogenosis type IV, childhood combined hepatic and myopathic form', 'GSD due to glycogen branching enzyme deficiency, childhood combined hepatic and myopathic form', 'GBE deficiency, childhood combined hepatic and myopathic form', 'GSD type 4, childhood combined hepatic and myopathic form', 'glycogen storage disease type IV, childhood combined hepatic and myopathic form', 'glycogen storage disease type 4, childhood combined hepatic and myopathic form', 'glycogenosis type 4, childhood combined hepatic and myopathic form', 'GSDIV, childhood combined hepatic and myopathic form']",,,308684,C0017922,"['-0.336', '0.224', '0.0898', '0.0671', '0.2344', '-0.287', '0.04425', '0.2281', '-0.1965', '0.00624', '-0.08856', '-0.0594', '-0.09845', '0.02275', '-0.1907', '-0.2708', '-0.1499', '-0.1868', '-0.4548', '-0.4395', '0.1046', '-0.3152', '0.3179', '-0.02782', '-0.1494', '-0.011635', '0.12036', '-0.1766', '-0.0626', '-0.02419', '0.2874', '0.2362', '0.2081', '0.02705', '-0.11414', '-0.335', '-0.00995', '0.00744', '0.0876', '-0.2264', '-0.1803', '-0.4463', '0.2205', '0.3394', '-0.3684', '-0.1161', '0.0821', '0.1416', '-0.079', '0.261', '0.05658', '-0.1127', '0.2556', '-0.06647', '-0.219', '-0.547', '0.264', '0.02385', '-0.286', '-0.04184', '0.2556', '0.0371', '0.2319', '-0.1148', '-0.02553', '-0.03513', '0.1794', '0.07745', '-0.3328', '-0.1213', '-0.3433', '0.012505', '0.01755', '0.0985', '0.2656', '0.2678', '-0.04156', '0.1543', '-0.3572', '-0.09424', '-0.098', '-0.1115', '0.0684', '0.027', '0.196', '0.11554', '0.319', '0.09973', '0.4421', '0.0893', '0.2123', '0.2683', '0.0644', '-0.0924', '0.6177', '0.4595', '0.2974', '-0.3777', '-0.0004666', '0.1554']",,,,,,10053250,
mondo:0017700,"glycogen storage disease due to glycogen branching enzyme deficiency, childhood neuromuscular form","['glycogen storage disease type 4, childhood neuromuscular form', 'GSDIV, childhood neuromuscular form', 'glycogen storage disease type IV, childhood neuromuscular form', 'glycogenosis type IV, childhood neuromuscular form', 'GSD due to glycogen branching enzyme deficiency, childhood neuromuscular form', 'glycogenosis type 4, childhood neuromuscular form', 'GSD type 4, childhood neuromuscular form', 'GBE deficiency, childhood neuromuscular form', 'glycogenosis due to glycogen branching enzyme deficiency, childhood neuromuscular form']",,,308698,C1856305,"['-0.4146', '0.1265', '-0.04495', '0.1741', '0.4417', '-0.248', '-0.1903', '0.2021', '-0.1621', '0.06995', '-0.00448', '-0.0615', '-0.03845', '0.11957', '-0.1808', '-0.2847', '-0.1953', '-0.2053', '-0.4587', '-0.3726', '0.177', '-0.1272', '0.4766', '-0.06683', '-0.1315', '-0.313', '0.1063', '-0.1509', '-0.09607', '-0.02455', '0.2196', '0.1622', '0.132', '0.2325', '-0.07544', '-0.1539', '-0.12286', '0.2102', '-0.03397', '-0.3203', '0.0988', '-0.2942', '0.09717', '0.1416', '-0.3606', '-0.1486', '0.02496', '0.1458', '0.02751', '0.3157', '0.09595', '-0.2761', '0.3586', '-0.09015', '-0.10583', '-0.534', '0.386', '0.11206', '-0.464', '0.02898', '0.157', '-0.01447', '0.3801', '-0.09436', '-0.2148', '0.2256', '0.2717', '0.05557', '-0.4434', '-0.0381', '-0.3032', '-0.01054', '0.09', '0.0783', '0.11475', '0.1957', '0.2257', '0.2686', '-0.4248', '-0.11804', '-0.2864', '-0.00453', '-0.04892', '0.02058', '0.1654', '0.1109', '0.3174', '0.0891', '0.3188', '0.1494', '0.0879', '0.3257', '-0.0296', '-0.05887', '0.4995', '0.308', '0.2913', '-0.312', '-0.10394', '0.2324']",,,,,,,
mondo:0017701,"glycogen storage disease due to glycogen branching enzyme deficiency, adult neuromuscular form","['glycogen storage disease type IV, adult neuromuscular form', 'GSDIV, adult neuromuscular form', 'GSD type 4, adult neuromuscular form', 'GBE deficiency, adult neuromuscular form', 'glycogenosis type IV, adult neuromuscular form', 'GSD due to glycogen branching enzyme deficiency, adult neuromuscular form', 'glycogen storage disease type 4, adult neuromuscular form', 'glycogenosis due to glycogen branching enzyme deficiency, adult neuromuscular form', 'glycogenosis type 4, adult neuromuscular form']",,,308712,CN203601,"['-0.3945', '0.1509', '0.00128', '0.2104', '0.4683', '-0.263', '-0.1926', '0.2002', '-0.1179', '0.07623', '0.0178', '-0.0663', '-0.01726', '0.1505', '-0.155', '-0.2876', '-0.1799', '-0.194', '-0.4863', '-0.35', '0.199', '-0.1483', '0.4314', '-0.0919', '-0.1448', '-0.3271', '0.0964', '-0.2042', '-0.01595', '0.00672', '0.2102', '0.141', '0.1176', '0.1757', '-0.0635', '-0.2047', '-0.0858', '0.2125', '-0.0909', '-0.325', '0.0743', '-0.31', '0.09064', '0.1572', '-0.3735', '-0.1364', '0.03137', '0.1631', '0.01188', '0.3123', '0.0873', '-0.2913', '0.2903', '-0.0857', '-0.17', '-0.5474', '0.3977', '0.07654', '-0.4822', '0.01449', '0.1987', '-0.03897', '0.3582', '-0.07996', '-0.2439', '0.199', '0.272', '-0.02371', '-0.3906', '-0.122', '-0.2974', '-0.0387', '0.10767', '0.03558', '0.1412', '0.1787', '0.2374', '0.2527', '-0.4824', '-0.0923', '-0.2732', '0.02269', '-0.06177', '0.00396', '0.1709', '0.1212', '0.3086', '0.10236', '0.239', '0.1013', '0.0939', '0.3086', '0.00706', '-0.0501', '0.5117', '0.2952', '0.2842', '-0.3223', '-0.11194', '0.247']",,,,,,,
mondo:0017703,disorder of glyoxylate metabolism,['disorder of glyoxylate metabolism'],,,308998,CN227177,,,,,,,,
mondo:0017704,familial partial epilepsy,"['epilepsy, partial, familial', 'hereditary partial epilepsy']",,,309,CN227178,,,,,,,,
mondo:0017705,congenital pulmonary venous return anomaly,"['scimitar syndrome', 'total anomalous pulmonary venous return', 'scimitar anomaly', 'TAPVR1', 'anomalous pulmonary venous return', 'TAPVR', 'APVR', 'congenital pulmonary venous connection anomaly', 'pulmonary venous return anomaly']",,,3090,,,,,,,,,
mondo:0017706,disorder of carbohydrate transmembrane transport and absorption,['disorder of carbohydrate absorption and transport'],,,309001,CN227180,,,,,,,,
mondo:0017708,mevalonate kinase deficiency,,,,309025,,,,,D054078,,,10072221,
mondo:0017709,disorder of lipid absorption and transport,,,,309028,CN227181,,,,,,,,
mondo:0017710,congenital systemic veins anomaly,,,,3091,,,,,,,,,
mondo:0017711,pancreatic colipase deficiency,,,,309108,C0268241,"['-0.1583', '-0.01147', '-0.0403', '0.02888', '0.2299', '-0.322', '-0.2947', '0.3853', '0.0669', '-0.1299', '-0.3047', '-0.1208', '-0.03705', '0.0397', '-0.1854', '-0.2686', '-0.0016775', '0.04633', '-0.4836', '-0.4692', '-0.004612', '-0.4226', '0.3252', '-0.2368', '0.1006', '-0.0671', '-0.0438', '0.04956', '0.05457', '-0.3186', '0.1124', '-0.0859', '-0.04303', '0.2496', '0.0678', '-0.0699', '-0.0884', '-0.3062', '0.0908', '0.07416', '-0.0827', '-0.2644', '0.2407', '-0.228', '-0.1582', '-0.3374', '0.2026', '0.00856', '-0.2393', '0.01604', '-0.0755', '-0.04138', '0.2527', '0.345', '-0.03937', '0.01811', '0.2715', '-0.1559', '-0.3696', '0.1871', '0.3328', '0.1008', '-0.00221', '-0.4011', '0.2319', '-0.05756', '0.1858', '0.4604', '-0.02904', '0.06', '-0.1537', '-0.1148', '-0.2893', '-0.004818', '0.2905', '0.0638', '0.1433', '-0.202', '0.04468', '0.1786', '-0.002445', '0.1307', '0.0754', '0.1768', '0.1506', '0.06168', '0.1174', '0.154', '0.5283', '-0.1333', '0.5776', '0.1493', '-0.1404', '-0.2622', '0.4387', '0.2129', '0.311', '-0.3625', '0.09576', '0.1242']",,,,277.89,K90.3,,
mondo:0017712,combined pancreatic lipase-colipase deficiency,,,,309111,,"['-0.41', '0.1754', '0.01444', '0.1533', '0.1367', '-0.259', '-0.4004', '0.4004', '0.07367', '-0.0727', '-0.05402', '-0.1592', '-0.1051', '0.001138', '-0.071', '-0.08215', '-0.05927', '0.1968', '-0.6064', '-0.358', '0.04163', '-0.6455', '0.2756', '-0.1873', '0.1504', '-0.277', '0.1061', '0.1221', '0.0786', '-0.4128', '0.3494', '0.00897', '0.03354', '0.1423', '0.00647', '-0.01563', '0.027', '-0.1608', '0.1255', '0.0685', '-0.2021', '-0.1326', '0.0436', '-0.2327', '-0.2488', '-0.3062', '0.2435', '0.05557', '-0.08105', '0.05905', '-0.05966', '-0.3018', '0.188', '0.2693', '-0.2194', '0.02527', '0.1292', '-0.3638', '-0.3472', '0.32', '0.4695', '0.002579', '0.096', '-0.4412', '0.0884', '0.11646', '0.2161', '0.2056', '-0.1937', '0.1182', '0.03232', '-0.05423', '-0.1493', '-0.2355', '0.3455', '-0.1682', '0.03638', '-0.1304', '0.014854', '0.288', '-0.02728', '-0.2844', '0.006123', '0.06323', '0.01002', '0.154', '0.08844', '0.0926', '0.5767', '-0.1073', '0.533', '0.2131', '-0.2898', '-0.0716', '0.334', '-0.01917', '0.06726', '-0.59', '0.0603', '0.1862']",,,,,K90.3,,
mondo:0017713,disorder of fatty acid oxidation and ketogenesis,,,,309115,CN227183,,,,,,,,
mondo:0017714,acyl-CoA dehydrogenase deficiency,,,,309120,C0268635,,,,,,,,
mondo:0017715,3-hydroxyacyl-CoA dehydrogenase deficiency,,,231530,309127,,"['-0.2644', '0.2793', '-0.01032', '0.19', '0.1389', '-0.1421', '0.03912', '-0.06198', '-0.1473', '-0.2148', '0.006485', '-0.0643', '0.1887', '0.3262', '-0.3547', '-0.3164', '-0.0811', '0.0874', '-0.3806', '-0.3833', '-0.0625', '-0.0908', '0.3276', '-0.1427', '-0.092', '-0.205', '0.0043', '-0.03032', '-0.0761', '-0.1854', '0.2068', '0.0802', '0.11523', '-0.06033', '-0.2815', '-0.2024', '-0.04654', '-0.04254', '-0.1282', '-0.427', '0.04388', '-0.3948', '0.05115', '-0.07477', '-0.1603', '-0.2522', '0.3809', '-0.1455', '0.3667', '0.4204', '-0.00696', '-0.1815', '0.1431', '0.1316', '-0.01501', '-0.3186', '0.3813', '0.0556', '-0.299', '0.0427', '0.3608', '0.0214', '0.2072', '0.1307', '0.1256', '0.0922', '0.3406', '-0.07623', '-0.518', '-0.0616', '-0.1626', '0.07263', '0.0556', '-0.07996', '0.1592', '0.468', '0.1156', '-0.08923', '-0.0646', '-0.0534', '0.01516', '-0.0643', '-0.06033', '0.0187', '0.0938', '0.2505', '-0.1158', '-0.09875', '0.5586', '-0.0863', '0.07245', '0.2896', '-0.307', '0.0635', '0.1836', '0.3376', '0.1315', '-0.1886', '-0.1421', '0.255']",,,C535310,,,,
mondo:0017716,disorder of carnitine cycle and carnitine transport,,,,309130,CN227184,,,,,,,,
mondo:0017719,gangliosidosis,,2368,,309144,C0017083,,,,,,,,
mondo:0017720,GM2 gangliosidosis,"['gangliosidosis GM2', 'GM>2< gangliosidosis', 'GM2-gangliosidosis, B, B1, AB variant']",3321,,309152,C0268274,,,,D020143,,E75.0,,
mondo:0017721,"Sandhoff disease, infantile form","['Hexosaminidases A and B deficiency, infantile form', 'infantile GM2 gangliosidosis 0 variant']",,,309155,CN203617,"['-0.3728', '0.3591', '0.0694', '0.09906', '0.173', '-0.2131', '-0.0919', '-0.2047', '-0.1506', '0.0866', '-0.216', '-0.06113', '0.02904', '-0.01575', '0.003609', '-0.1647', '-0.06464', '-0.1122', '-0.1478', '-0.1696', '0.1531', '-0.2374', '0.395', '0.0493', '0.06143', '-0.135', '-0.0766', '-0.1575', '-0.298', '0.01387', '0.2952', '0.2098', '0.2708', '0.0607', '0.1952', '-0.1901', '-0.04724', '0.1313', '-0.1456', '-0.3796', '-0.12274', '-0.4087', '0.2888', '0.0913', '-0.1785', '-0.421', '0.1638', '-0.02022', '0.144', '0.2454', '0.1539', '-0.01785', '-0.11456', '0.01904', '-0.0439', '-0.4302', '0.3452', '-0.1066', '-0.4097', '0.2043', '0.1552', '0.0626', '0.2283', '0.1063', '0.08264', '-0.04385', '0.2937', '0.02393', '-0.289', '-0.0365', '-0.1509', '0.01807', '0.0368', '0.06995', '0.2463', '0.2634', '0.01569', '0.37', '-0.355', '-0.0867', '-0.01978', '-0.1067', '-0.164', '0.1533', '-0.00958', '-0.10223', '0.1615', '0.1182', '0.1641', '-0.2644', '0.3276', '0.2349', '-0.2133', '-0.08813', '0.3535', '0.3352', '0.2864', '-0.4177', '-0.07794', '0.1398']",,,,,,,
mondo:0017722,"Sandhoff disease, juvenile form","['Hexosaminidases A and B deficiency, juvenile form', 'juvenile GM2 gangliosidosis 0 variant']",,,309162,CN203618,"['-0.4011', '0.3877', '0.07367', '0.1328', '0.1804', '-0.2084', '-0.081', '-0.1637', '-0.1388', '0.0799', '-0.1975', '-0.0367', '0.01859', '-0.015495', '0.010124', '-0.1648', '-0.07654', '-0.10547', '-0.1477', '-0.1991', '0.156', '-0.2284', '0.3767', '0.013', '0.0497', '-0.0923', '-0.0856', '-0.1337', '-0.2961', '0.02179', '0.279', '0.1873', '0.2336', '0.07367', '0.2443', '-0.1892', '-0.04578', '0.12354', '-0.1411', '-0.3308', '-0.1118', '-0.4446', '0.2742', '0.1012', '-0.1387', '-0.3828', '0.1606', '-0.01826', '0.2151', '0.2235', '0.1582', '-0.02127', '-0.10425', '0.05087', '-0.05835', '-0.4597', '0.343', '-0.0875', '-0.437', '0.202', '0.2225', '0.09106', '0.1938', '0.1061', '0.10815', '-0.0471', '0.3071', '0.01261', '-0.2727', '0.01851', '-0.1799', '-0.05484', '0.0324', '0.05914', '0.2261', '0.246', '-0.004837', '0.3896', '-0.3738', '-0.1478', '0.001902', '-0.1746', '-0.1433', '0.1589', '-0.08246', '-0.11835', '0.1667', '0.1129', '0.1876', '-0.2734', '0.298', '0.2201', '-0.1965', '-0.09753', '0.3975', '0.3079', '0.3066', '-0.43', '-0.12115', '0.1571']",,,,,,,
mondo:0017723,"Sandhoff disease, adult form","['Hexosaminidases A and B deficiency, adult form', 'adult Sandhoff disease', 'adult GM2 gangliosidosis 0 variant', 'Sandhoff disease of adults']",,,309169,CN203619,"['-0.424', '0.4277', '0.00962', '0.07983', '0.2551', '-0.2554', '-0.1389', '-0.1798', '-0.1531', '0.04333', '-0.2103', '0.003784', '0.02353', '0.01284', '-0.0415', '-0.17', '-0.1282', '-0.1329', '-0.2108', '-0.1509', '0.1377', '-0.2524', '0.3616', '0.0601', '0.04373', '-0.1431', '-0.0913', '-0.189', '-0.253', '0.0807', '0.2476', '0.1716', '0.2438', '0.04803', '0.2856', '-0.2517', '-0.01587', '0.1981', '-0.159', '-0.4236', '-0.1547', '-0.4749', '0.2886', '0.05908', '-0.1877', '-0.4377', '0.1993', '-0.02533', '0.1827', '0.2491', '0.21', '0.002447', '-0.1517', '0.05743', '-0.0643', '-0.558', '0.4133', '-0.1421', '-0.4358', '0.2133', '0.2556', '0.11993', '0.2466', '0.1492', '0.07654', '0.02461', '0.307', '-0.02869', '-0.278', '-0.0506', '-0.2063', '-0.01892', '0.10986', '0.04074', '0.3125', '0.2379', '-0.05847', '0.5176', '-0.4517', '-0.1505', '0.00899', '-0.10175', '-0.1661', '0.11786', '-0.0101', '-0.1382', '0.11755', '0.11084', '0.1573', '-0.295', '0.2737', '0.2429', '-0.158', '-0.04303', '0.3843', '0.3508', '0.2761', '-0.5195', '-0.0696', '0.1213']",,,,,,,
mondo:0017724,"Tay-Sachs disease, b variant, infantile form","['GM2 gangliosidosis, B variant, infantile form', 'hexosaminidase A deficiency, infantile form']",,,309178,CN203620,,,,,,,,
mondo:0017725,"Tay-Sachs disease, b variant, juvenile form","['hexosaminidase A deficiency, juvenile form', 'GM2 gangliosidosis, B variant, juvenile form']",,,309185,CN203621,,,,,,,,
mondo:0017726,"Tay-Sachs disease, B variant, adult form","['GM2 gangliosidosis, B variant, adult form', 'hexosaminidase A deficiency, adult form']",,,309192,C1848914,,,,,,,,
mondo:0017727,fixed subaortic stenosis,,,,3092,,,,,,,,,
mondo:0017728,"Tay-Sachs disease, B1 variant","['hexosaminidase A deficiency, B1 variant', 'GM2 gangliosidosis, B1 variant']",,,309239,,,,,,,,,
mondo:0017729,"metachromatic leukodystrophy, late infantile form","['arylsulfatase A deficiency, late infantile form', 'MLD, late infantile form']",,,309256,,,,,,,,,
mondo:0017730,"metachromatic leukodystrophy, adult form","['arylsulfatase A deficiency, adult form', 'MLD, adult form']",,,309271,,,,,,,,,
mondo:0017731,glycoproteinosis,,,,309279,,,,,,,,,
mondo:0017732,"alpha-mannosidosis, infantile form","['lysosomal alpha-D-mannosidase deficiency, infantile form']",,,309282,,,,,,,,,
mondo:0017733,"alpha-mannosidosis, adult form","['lysosomal alpha-D-mannosidase deficiency, adult form', 'Alpha-mannosidosis adult-onset form']",,,309288,CN036949,,,,,,,,
mondo:0017734,sialidosis,,,,309294,,,,,,,,10058800,
mondo:0017735,congenital aortic valve stenosis,,,,3093,,,,,,746.3,,10010371,
mondo:0017736,disorder of sialic acid metabolism,,,,309319,C0342851,,,,,277.89,,,
mondo:0017737,intermediate severe Salla disease,['Intermediate Salla disease'],,,309331,CN203640,,,,,,,,
mondo:0017738,lysosomal glycogen storage disease,,,,309337,CN203642,,,,,,E74.0,,
mondo:0017739,disorder of lysosomal-related organelles,,,,309340,CN227186,,,,,,,,
mondo:0017740,disorder of protein N-glycosylation,"['disorder of protein N-linked glycosylation', 'protein N-linked glycosylation disease']",,,309347,CN227187,,,,,,,,
mondo:0017741,disorder of protein O-glycosylation,"['disorder of protein O-linked glycosylation', 'protein O-linked glycosylation disease']",,,309447,CN227188,,,,,,,,
mondo:0017742,disorder of O-xylosylglycan synthesis,,,,309450,CN227189,,,,,,,,
mondo:0017743,disorder of O-N-acetylgalactosaminylglycan synthesis,,,,309458,CN227190,,,,,,,,
mondo:0017744,disorder of O-xylosyl/N-acetylgalactosaminylglycan synthesis,,,,309463,CN227191,,,,,,,,
mondo:0017745,disorder of O-mannosylglycan synthesis,,,,309469,CN227192,,,,,,,,
mondo:0017746,atypical Rett syndrome,"['atypical RTT', 'Rett like syndrome', 'Rett syndrome variant']",,,3095,C2748910,"['-0.10443', '-0.11017', '-0.0913', '0.6787', '-0.0744', '-0.5776', '0.3955', '0.8154', '-0.3447', '-0.4712', '-0.2507', '-0.04172', '0.10626', '0.532', '0.4988', '0.1805', '-0.1077', '-0.00772', '-0.1754', '-0.6094', '0.1523', '-0.2917', '0.345', '-0.5938', '0.507', '-0.4836', '0.1835', '-0.2224', '0.322', '0.7534', '0.3647', '-0.507', '0.6577', '0.2191', '-0.3052', '-0.04108', '-0.3206', '0.1553', '0.4695', '0.01712', '0.4902', '-0.06155', '-0.4883', '0.2812', '0.745', '-0.529', '-0.951', '0.1483', '0.076', '0.723', '-0.552', '-0.2279', '-0.605', '-0.2051', '0.2932', '-0.4717', '-0.4202', '0.3188', '-0.324', '0.05386', '0.2191', '0.1343', '0.5234', '0.7705', '-0.2842', '0.1572', '0.2607', '0.04718', '-0.2954', '0.562', '-0.01015', '-0.3267', '-0.04337', '-0.671', '0.05774', '0.5425', '-0.6426', '0.5063', '-0.0595', '0.1293', '0.4143', '-0.0923', '0.1547', '0.002092', '0.4014', '-0.0705', '0.413', '0.3914', '0.8115', '0.3845', '-0.1447', '0.11743', '0.01653', '0.6665', '-0.3154', '0.1864', '0.133', '-0.57', '0.58', '0.1576']",,,,,,,
mondo:0017747,disorder of fucoglycosan synthesis,,,,309505,CN227193,,,,,,,,
mondo:0017748,inborn disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation,"['disorder of glycosphingolipid and GPI-anchored proteins glycosylation', 'disorder of glycosphingolipid and glycosylphosphatidylinositol anchor glycosylation']",,,309515,CN227194,"['-0.1687', '0.1091', '0.07367', '-0.02423', '0.05576', '-0.1628', '-0.009636', '0.02972', '-0.11786', '0.005627', '-0.03305', '-0.02042', '0.04877', '-0.0659', '-0.0842', '-0.02892', '0.05127', '-0.0822', '-0.06476', '-0.2277', '-0.01582', '0.00508', '0.1328', '-0.0958', '0.05365', '-0.01689', '-0.0234', '-0.04355', '0.06854', '-0.1112', '0.04523', '0.0997', '0.1117', '0.1176', '-0.01047', '-0.05615', '-0.007256', '0.01202', '-0.0641', '-0.1768', '0.02269', '-0.1526', '0.01656', '-0.02583', '-0.06604', '-0.179', '0.02687', '0.1376', '0.05734', '0.0645', '-0.0606', '-0.0211', '0.01657', '0.0518', '-0.1273', '-0.0753', '0.11884', '0.02533', '-0.1931', '0.05292', '0.06094', '0.07733', '0.0573', '-0.00544', '0.01474', '-0.05707', '0.11536', '0.08813', '-0.1719', '0.05536', '-0.09064', '0.08905', '0.00667', '-0.0467', '0.01459', '0.0868', '0.06354', '-0.01843', '-0.1538', '-0.02127', '0.04547', '-0.015564', '-0.0658', '0.1321', '0.00414', '-0.03763', '0.0175', '0.11694', '0.1074', '-0.04095', '0.04306', '0.1382', '-0.01167', '-0.006702', '0.1707', '0.1076', '0.1788', '-0.1835', '0.02061', '0.08234']",,,,,,,
mondo:0017749,disorder of multiple glycosylation,,,,309526,CN227195,,,,,,,,
mondo:0017750,defect in conserved oligomeric Golgi complex,['defect in COG complex'],,,309568,,,,,,,,,
mondo:0017752,defect in V-ATPase,,,,309778,,,,,,,,,
mondo:0017754,inborn disorder of porphyrin metabolism,"['inborn disorder of porphyrin and haem metabolism', 'rare inborn error of porphyrin-containing compound metabolic process', 'disorder of porphyrin and haem metabolism', 'inborn error of porphyrin-containing compound metabolic process']",,,309813,C1275125,,,,,,E80.4,,
mondo:0017755,inborn disorder of bilirubin metabolism,"['disorder of bilirubin metabolism', 'hereditary bilirubin metabolism disease']",,,309816,CN227200,"['-0.09155', '0.2277', '-0.01289', '0.1321', '0.1368', '-0.192', '-0.173', '0.0945', '-0.1459', '-0.006542', '0.0855', '0.01412', '0.1395', '-0.1177', '-0.1503', '-0.2079', '-0.03458', '-0.009254', '-0.11694', '-0.529', '-0.01964', '-0.1295', '0.2352', '-0.00173', '0.06158', '-0.05872', '0.1812', '0.01011', '-0.00862', '0.0339', '0.03342', '0.0492', '0.1559', '0.02007', '-0.224', '-0.010315', '0.03152', '-0.0687', '0.05655', '-0.2668', '0.1746', '-0.283', '0.1567', '-0.06805', '-0.1037', '-0.1843', '0.06525', '-0.01124', '0.274', '0.1648', '-0.1044', '-0.0844', '-0.05423', '0.0658', '0.0013895', '-0.2212', '0.254', '0.1465', '-0.474', '-0.02444', '0.305', '0.0333', '0.3137', '-0.094', '0.02048', '0.03928', '0.266', '0.1101', '-0.2595', '0.10815', '-0.2961', '0.04047', '0.00913', '0.02393', '0.06964', '0.2637', '-0.047', '0.07355', '-0.262', '-0.1458', '0.02185', '0.07306', '-0.005985', '0.0734', '0.0701', '-0.01334', '0.088', '0.0688', '0.1595', '0.0662', '0.1252', '0.1857', '-0.088', '-0.0879', '0.275', '0.278', '0.2164', '-0.3418', '-0.1102', '0.1584']",,,,,,,
mondo:0017756,disorder of pterin metabolism,,,,309819,CN227201,,,,,,,,
mondo:0017757,disorder of metabolite absorption and transport,,,,309824,CN227202,,,,,,,,
mondo:0017758,disorder of vitamin and non-protein cofactor absorption and transport,['disorder of vitamin and non-protein cofactor absorption and transport'],,,309827,CN227203,,,,,,,,
mondo:0017759,disorder of catecholamine synthesis,,,,309830,C0342685,,,,,270.8,,,
mondo:0017760,disorder of other vitamins and cofactors metabolism and transport,,,,309833,CN227204,,,,,,,,
mondo:0017761,disorder of mineral absorption and transport,,,,309836,CN227205,,,,,,E83.3,,
mondo:0017762,disorder of copper metabolism,"['rare inborn error of cellular copper ion homeostasis', 'copper Transport disorders', 'inborn error of cellular copper ion homeostasis']",,,309839,CN043585,,,,,275.1,,10061091,
mondo:0017763,disorder of iron metabolism and transport,,,,309842,CN227206,,,,,,E83.1,,
mondo:0017764,disorder of zinc metabolism,['disorder of zinc metabolism and transport'],,,309845,,,,,,275.8,,10048260,
mondo:0017765,disorder of magnesium transport,"['rare inborn error of magnesium ion transport', 'inborn error of magnesium ion transport']",,,309848,CN227207,,,,,,,,
mondo:0017766,disorder of manganese transport,,,,309851,CN227208,,,,,,,,
mondo:0017767,rheumatic fever,"['ARF', 'RHF - rheumatic fever', 'acute rheumatic fever', 'inflammatory rheumatism']",1586,,3099,C0035436,,C34984,1001160,D012213,390-392.99,I00-I02,10039054,
mondo:0017768,reflex epilepsy,"['epilepsy, sensory-induced']",2548,,310,C0270857,,C85041,1001146,D020195,345.10,,,
mondo:0017769,acquired immunodeficiency,,,,310050,,,,,,,,,
mondo:0017770,Robinow-like syndrome,['Saal-Greenstein syndrome'],,,3105,CN203671,,,,,,,,
mondo:0017771,Mayer-Rokitansky-Kuster-Hauser syndrome,"['Rokitansky syndrome', 'MRKH syndrome', 'Mayer-Rokitansky-Küster-Hauser syndrome', 'Mullerian aplasia/dysgenesis', 'MRKH']",0112177,,3109,,,C124853,,,,,10065148,
mondo:0017772,oral erosive lichen,,,,31142,CN203692,,,,,,,,
mondo:0018426,AXIN2-related attenuated familial adenomatous polyposis,"['AXIN2-related attenuated familial polyposis coli', 'AXIN2-related attenuated FAP', 'AXIN2-related AFAP']",,,401911,CN226139,,,,,,,,
mondo:0018428,9q31.1q31.3 microdeletion syndrome,"['Del(9)(q31.1q31.3)', 'monosomy 9q31.1q31.3']",,,401923,CN226140,,,,,,,,
mondo:0018429,14q24.1q24.3 microdeletion syndrome,"['Del(14)(q24.1q24.3)', 'monosomy 14q24.1q24.3']",,,401935,CN226142,,,,,,,,
mondo:0018430,partial corpus callosum agenesis-cerebellar vermis hypoplasia with posterior fossa cysts syndrome,,,,401959,CN226145,,,,,,,,
mondo:0018431,cold-induced sweating syndrome - hyperthermia spectrum,,,,401993,CN226150,,,,,,,,
mondo:0018432,lichen myxedematosus,"['papular mucinosis', 'lichen myxoedematosus']",,,402007,,,,,,701.8,,,
mondo:0018433,acute myeloid leukemia with t(6;9)(p23;q34),['AML with t(6;9)(p23;q34)'],,,402014,,,,,,,,,
mondo:0018434,acute myeloid leukemia with t(9;11)(p22;q23),['AML with t(9;11)(p22;q23)'],,,402017,,,,,,,,,
mondo:0018435,acute myeloid leukemia with inv3(p21;q26.2) or t(3;3)(p21;q26.2),"['acute myeloid leukemia with inv3(q21;q26.2) or t(3;3)(q21;q26.2)', 'AML with inv3(q21;q26.2) or t(3;3)(q21;q26.2)', 'acute myeloid leukaemia with inv3(q21;q26.2) or t(3;3)(q21;q26.2)', 'AML with inv3(p21;q26.2) or t(3;3)(p21;q26.2)']",,,402020,,,,,,,,,
mondo:0018436,megakaryoblastic acute myeloid leukemia with t(1;22)(p13;q13),['megakaryoblastic AML with t(1;22)(p13;q13)'],,,402023,,,,,,,,,
mondo:0018437,acute myeloid leukemia with NPM1 somatic mutations,['AML with NPM1 somatic mutations'],,,402026,,,,,,,,,
mondo:0018438,eosinophilic gastrointestinal disease,"['primary eosinophilic gastrointestinal disease', 'EGID']",,,402029,CN226154,,,,,,,,
mondo:0018439,eosinophilic colitis,,,,402035,C0267448,,C27053,,,558.42,K52.82,,
mondo:0018440,autosomal recessive distal renal tubular acidosis,"['AR dRTA', 'autosomal recessive distal RTA', 'distal renal tubular acidosis (disease), autosomal recessive']",,,402041,C1864498,"['-0.2996', '-0.1298', '-0.478', '-0.3545', '0.01747', '-0.3396', '-0.3196', '0.897', '-0.1362', '0.0336', '-0.3235', '0.11926', '-0.2712', '0.601', '-0.4072', '-0.2864', '-0.06824', '-0.2886', '0.04025', '-0.9316', '-0.2715', '-0.7524', '0.2352', '0.1573', '0.8667', '-0.0935', '-0.1377', '-0.03036', '0.03308', '-0.02892', '0.12396', '-0.1595', '0.2164', '0.11224', '-0.53', '-0.3003', '-0.278', '-0.008484', '0.0978', '0.451', '-0.1682', '-0.07825', '0.4595', '0.2937', '-0.0857', '-0.3962', '-0.5527', '-0.05484', '0.0981', '0.3674', '0.3655', '-0.0247', '0.4707', '-0.238', '0.085', '-0.5503', '0.5215', '-0.2385', '-0.7036', '0.65', '0.609', '-0.1715', '0.1228', '-0.3167', '-0.4023', '0.1345', '0.2568', '0.5454', '-0.1021', '0.5244', '-0.1803', '-0.502', '0.192', '-0.2678', '0.572', '-0.3506', '0.292', '0.1517', '-0.04675', '0.1237', '-0.08887', '-0.2974', '0.2463', '0.0701', '0.3286', '0.3945', '-0.1791', '-0.2374', '0.3347', '0.4683', '0.3792', '0.2573', '-0.02792', '-0.06082', '0.258', '0.05603', '0.855', '-0.2537', '-0.2908', '0.1343']",,,,,,,
mondo:0018442,acitretin/etretinate embryopathy,"['foetal acitretin/etretinate syndrome', 'fetal acitretin syndrome', 'retinoid embryopathy', 'acitretin embryopathy', 'acitretin embryofetopathy', 'Acitretine embryofetopathy', 'foetal acitretin syndrome', 'fetal acitretin/etretinate syndrome']",,,40366,CN205049,,,,C538169,,,,
mondo:0018443,FBLN1-related developmental delay-central nervous system anomaly-syndactyly syndrome,,,,404451,CN226185,,,,,,,,
mondo:0018445,global developmental delay - lung cysts - overgrowth - Wilms tumor syndrome,"['global developmental delay, lung cysts, overgrowth, and wilms tumor', 'GLOW', 'glow syndrome', 'global developmental delay, lung cysts, overgrowth, and wilms tumour', 'GLOW syndrome, somatic mosaic']",,618272,404476,CN226190,"['-0.3022', '0.02728', '0.4675', '-0.167', '0.2715', '-0.2573', '-0.01646', '0.2693', '-0.4373', '0.03366', '-0.1393', '-0.1002', '0.3098', '-0.0709', '-0.33', '-0.0619', '0.3345', '-0.1682', '-0.08057', '-0.4844', '0.009705', '-0.2343', '0.2656', '-0.2452', '0.2695', '-0.3638', '-0.1515', '0.275', '0.3418', '-0.2123', '0.3245', '-0.1681', '0.6304', '0.0467', '0.104', '-0.0405', '-0.3552', '0.05005', '0.007538', '-0.4363', '-0.0863', '-0.1304', '0.02698', '0.1179', '0.1693', '-0.1174', '-0.01406', '0.5376', '-0.1527', '0.02415', '-0.4214', '0.3037', '-0.1215', '0.3582', '-0.4343', '0.0098', '-0.274', '-0.1523', '-0.2457', '0.1089', '0.2898', '0.02989', '-0.612', '0.1992', '-0.1101', '-0.0595', '0.2079', '0.3723', '-0.1594', '0.3542', '-0.4792', '0.535', '0.2457', '0.28', '-0.4856', '-0.07227', '0.456', '-0.2092', '-0.258', '-0.547', '-0.2135', '0.0949', '-0.1686', '0.4255', '-0.122', '-0.05972', '-0.239', '0.3916', '0.182', '0.1392', '0.05685', '0.568', '0.1404', '-0.01434', '0.547', '-0.0002966', '0.4907', '-0.1898', '0.4578', '0.3074']",,,,,,,
mondo:0018446,autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome,,,,404481,CN226191,,,,,,,,
mondo:0018447,chondromyxoid fibroma,['Chondromyxoid fibroma'],,,404507,C0221290,,C3830,0000332,,,,,
mondo:0018448,clear cell papillary renal cell carcinoma,,,,404511,C4518333,,,,,,,,
mondo:0018449,acquired cystic disease-associated renal cell carcinoma,,,,404514,CN226194,,C157718,,,,,,
mondo:0018450,spinal muscular atrophy with respiratory distress type 2,"['severe infantile axonal neuropathy with respiratory failure type 2', 'SMARD2', 'diaphragmatic spinal muscular atrophy type 2', 'X-linked spinal muscular atrophy with respiratory distress']",,,404521,CN226195,,,,,,,,
mondo:0018451,X-linked distal hereditary motor neuropathy,"['X-linked dHMN', 'X-linked distal spinal muscular atrophy', 'distal hereditary motor neuropathy, X-linked']",,,404538,,,,,,,,,
mondo:0018453,familial atypical multiple mole melanoma syndrome,"['FAMMM syndrome', 'familial atypical mole syndrome', 'familial atypical mole melanoma syndrome', 'FAMM-PC syndrome', 'familial atypical multiple mole melanoma-pancreatic carcinoma syndrome', 'familial dysplastic nevus syndrome', 'FAMM syndrome', 'melanoma-pancreatic cancer syndrome', 'B-K mole syndrome', 'familial Clark nevus syndrome']",,,404560,C2314896,"['0.448', '0.04825', '-0.9097', '0.2045', '0.6016', '-0.004364', '-0.093', '0.4146', '-0.3884', '-0.2205', '0.883', '0.02606', '-0.4656', '0.4136', '-0.792', '-0.2764', '0.1693', '-0.6816', '0.0662', '0.1107', '-0.1991', '0.2446', '-0.1318', '-0.2324', '0.2925', '-0.438', '-0.674', '-0.2363', '0.4023', '0.1295', '1.054', '-0.435', '-0.0463', '-0.1968', '0.2874', '0.645', '-0.3909', '-0.1293', '0.04193', '-0.2522', '0.422', '-0.7495', '-0.02504', '-0.3276', '0.1663', '-0.4702', '-0.2472', '-0.4863', '-0.2634', '-0.6763', '-0.11176', '-0.2091', '0.0261', '-0.4102', '-0.649', '-0.3352', '-0.1144', '0.12213', '-0.726', '-0.5977', '0.02354', '0.08453', '-0.851', '0.4133', '0.2146', '1.216', '0.4055', '0.749', '0.3762', '0.8384', '0.11743', '0.5337', '0.3535', '0.2493', '0.589', '0.2207', '-0.6875', '0.2695', '-0.05374', '-0.1843', '0.2421', '-0.1857', '0.3738', '-0.2546', '-0.2866', '-0.942', '0.1447', '0.251', '1.027', '-0.1522', '0.8394', '0.1405', '-0.5947', '0.0834', '0.6294', '0.2969', '-0.238', '-0.7437', '-0.617', '0.581']",C27264,,,,,,
mondo:0018454,dysostosis of genetic origin,['genetic dysostosis'],,,404568,,,,,,,,,
mondo:0018456,polyarticular juvenile idiopathic arthritis,"['juvenile polyarticular arthritis', 'juvenile polyarthritis', 'polyarticular JIA']",,,404580,,,,1002020,,,,,
mondo:0018458,familial hypocalciuric hypercalcemia,"['familial benign hypocalciuric hypercalcemia', 'FBH', 'FHH', 'hypocalciuric hypercalcemia', 'familial benign hypercalcemia', 'FBHH']",0060699,,405,C1809471,"['0.1877', '0.2274', '0.4949', '-0.08514', '-0.2874', '0.2964', '-0.2727', '0.589', '-0.2081', '-0.1548', '0.03075', '0.2917', '-0.304', '0.8037', '-0.1581', '-0.5337', '-0.512', '-0.01522', '-0.0965', '-0.577', '0.4553', '-0.556', '0.0169', '-0.588', '0.6704', '-0.5747', '0.8584', '-0.679', '0.2206', '-0.2263', '0.04514', '0.0723', '0.3938', '0.02672', '-1.095', '-0.3618', '-0.3694', '0.1265', '0.2874', '-0.2019', '0.2131', '-0.269', '0.2917', '-0.701', '0.4844', '-0.2751', '-0.3706', '-0.299', '-0.045', '0.761', '-0.1575', '0.4934', '0.4294', '-0.4956', '-0.6772', '0.4568', '-0.288', '0.564', '-0.0168', '0.41', '0.6494', '0.371', '-0.129', '-0.9272', '-0.3994', '0.06', '0.0224', '0.7314', '-0.3508', '0.1964', '0.376', '0.3438', '0.1667', '0.1418', '0.0308', '1.055', '0.1317', '1.184', '0.5493', '0.3745', '-0.591', '-0.4854', '0.3586', '0.1505', '-0.0681', '0.3523', '0.08655', '0.00925', '0.537', '0.2644', '0.315', '0.4375', '-0.8364', '-0.5093', '0.6836', '0.576', '0.4746', '-0.4526', '-0.6206', '0.02472']",C123262,,,,,,
mondo:0018459,isolated glycerol kinase deficiency,"['nonsyndromic inborn glycerol kinase deficiency', 'nonsyndromic glycerol kinase deficiency', 'hyperglycerolemia']",,,408,,"['-0.5635', '0.4578', '-0.4194', '0.00396', '0.265', '-0.2173', '-0.3943', '0.0815', '-0.1659', '0.1482', '-0.3616', '0.3345', '0.1451', '0.157', '-0.0785', '-0.08514', '-0.3113', '-0.09155', '0.05222', '-0.9004', '-0.1241', '-0.2208', '0.571', '0.1372', '-0.013695', '0.11127', '-0.02301', '-0.3076', '0.1471', '-0.383', '0.218', '0.3608', '0.6357', '0.3765', '0.0827', '-0.202', '-0.597', '-0.1936', '-0.2113', '-0.331', '0.11005', '-0.9155', '0.4436', '-0.4424', '-0.2382', '-0.336', '-0.1328', '0.227', '0.03513', '0.4648', '0.1677', '0.1768', '-0.08466', '-0.4016', '-0.1113', '-0.286', '0.4363', '-0.457', '-0.4155', '0.3215', '0.04425', '0.02553', '0.3076', '-0.5703', '0.3303', '0.136', '0.4536', '0.1298', '-0.3936', '-0.2012', '0.2283', '-0.3367', '0.0787', '-0.07294', '0.4504', '0.0475', '0.3083', '-0.2507', '0.06335', '-0.4114', '0.1544', '0.1216', '-0.2124', '-0.07434', '0.602', '0.2686', '-0.1041', '-0.2144', '0.7036', '0.0629', '0.2133', '0.507', '0.01656', '-0.1698', '0.4185', '0.4558', '0.5493', '-0.3286', '-0.2427', '0.1353']",,,,,,,
mondo:0018460,Eales disease,"['idiopathic retinal vasculitis', 'idiopathic recurrent vitreal hemorrhage', 'idiopathic recurrent vitreal haemorrhage', 'idiopathic retinal perivasculitis', 'idiopathic obliterative vasculopathy']",,,40923,C0271073,,,,C538011,,,10057429,
mondo:0018461,Angelman syndrome due to a point mutation,,,,411511,CN237441,,,,,,,,
mondo:0018462,Angelman syndrome due to imprinting defect in 15q11-q13,,,,411515,CN237442,,,,,,,,
mondo:0018463,mild phosphoribosylpyrophosphate synthetase superactivity,"['mild PRPS1 superactivity', 'mild PRPP synthetase superactivity']",,,411536,CN237443,,,,,,,,
mondo:0018464,severe phosphoribosylpyrophosphate synthetase superactivity,"['severe PRPP synthetase superactivity', 'severe PRPS1 superactivity']",,,411543,CN237444,,,,,,,,
mondo:0018465,insulin autoimmune syndrome,"['Hirata disease', 'insulin autoimmune hypoglycemia']",0040100,,411593,C0854359,,,,,279.49,,,
mondo:0018467,nephropathic infantile cystinosis,"['cystinosis, atypical nephropathic', 'CTNS', 'cystinosis, infantile nephropathic', 'lysosomal cystine transport protein, defect of', 'cystinosin, defect of']",,,411629,,,,,,,,,
mondo:0018468,proton-pump inhibitor-responsive esophageal eosinophilia,"['PPIRee', 'PPI-responsive esophageal eosinophilia', 'PPI-REE']",,,411696,,,,,,,,,
mondo:0018469,pulmonary non-tuberculous mycobacterial infection,"['non-tuberculous mycobacterial lung disease', 'nontuberculous mycobacterial lung disease']",,,411703,CN237452,,,,,,,,
mondo:0018470,renal agenesis,"['renal adysplasia', 'hereditary renal aplasia', 'renal hypodysplasia/aplasia', 'absent/underdeveloped kidney', 'hereditary urogenital adysplasia', 'renal aplasia', 'renal agenesis', 'renal agenesis (disease)', 'absent/small kidney', 'renal agenesis/hypoplasia']",14766,,411709,,,C99041,,,,,,0008678
mondo:0018471,generalized eruptive keratoacanthoma,"['GEKA', 'generalized eruptive keratoacanthomas of Grzybowski', 'Grzybowski syndrome', 'generalised eruptive keratoacanthomas of Grzybowski']",,,411777,CN237455,,,,,,,,
mondo:0018472,familial isolated trichomegaly,,0111566,,411788,,,,,,,,,
mondo:0018473,hyperlipoproteinemia type 3,"['dyslipidemia type 3', 'familial type 3 hyperlipoproteinemia', 'hyperlipoproteinemia, type III', 'remnant disease', 'dysbetalipoproteinemia due to defect in apolipoprotein E-D', 'apolipoprotein E, deficiency or defect of', 'remnant removal disease', 'familial hypercholesterolemia with hyperlipemia', 'HLP type 3', 'hyperlipidemia type 3', 'familial dysbetalipoproteinemia', 'hyperlipoproteinemia type III', 'dysbetalipoproteinemia', 'familial hyperlipoproteinemia type 3', 'low density lipoprotein cholesterol level quantitative trait locus 5', 'remnant hyperlipidemia', 'Broad-betalipoproteinemia', 'carbohydrate induced hyperlipemia', 'familial hypercholesterolaemia with hyperlipaemia', 'dyslipidaemia type 3', 'floating-betalipoproteinemia', 'hyperlipemia with Familial Hypercholesterolemic xanthomatosis', 'coronary artery disease, Severe, Susceptibility to', 'familial Hyperbeta- and Prebetalipoproteinemia', 'Broad beta disease']",3145,617347,412,C1862561,"['-0.0962', '0.163', '-0.4724', '0.11957', '0.4302', '-0.1006', '-0.1832', '0.2634', '-0.358', '-0.2676', '-0.4949', '-0.1458', '0.4158', '-0.2285', '-0.5093', '-0.837', '0.6787', '0.08527', '0.04517', '-0.0683', '-0.4617', '-0.5093', '0.728', '0.1794', '-0.04147', '0.3298', '0.11', '0.1687', '0.06415', '-0.3608', '1.183', '0.1777', '1.072', '0.518', '-0.0408', '-0.10834', '0.1193', '0.0734', '0.1376', '-0.2776', '-0.2568', '0.07465', '0.3125', '-0.04758', '-0.306', '0.1301', '0.08844', '0.2328', '0.2551', '0.1333', '-0.01773', '-0.0811', '0.1246', '-0.6562', '-0.3079', '-0.1707', '0.4841', '-0.716', '-0.4546', '-0.1595', '-0.4358', '0.3381', '0.0873', '-0.1686', '-0.02184', '0.49', '0.1239', '0.03857', '-0.301', '0.0728', '0.3328', '-0.742', '-0.04465', '0.2512', '0.1875', '0.504', '0.2314', '0.2048', '-0.2463', '-0.508', '-0.6685', '-0.5146', '0.0773', '0.04016', '0.351', '0.8687', '-0.062', '0.676', '0.8374', '0.06714', '-0.04883', '-0.06088', '-0.1929', '0.1364', '0.252', '0.2786', '0.4849', '0.2151', '-0.72', '-0.08215']",,,,,,10060751,
mondo:0018474,13q12.3 microdeletion syndrome,"['monosomy 13q12.3', 'Del(13)(q12.3)']",,,412035,CN237459,,,,,,,,
mondo:0018475,PRKAR1B-related neurodegenerative dementia with intermediate filaments,,,,412066,CN237461,,,,,,,,
mondo:0018476,dystonia-aphonia syndrome,,,,412217,CN237465,,,,,,,,
mondo:0018477,bilirubin encephalopathy,"['kernicterus', 'kernicterus spectrum disorder', 'bilirubin encephalopathy', 'hyperbilirubinemic encephalopathy']",2382,,415286,,,C84799,1001002,D007647,,,10023376,
mondo:0018479,congenital adrenal hyperplasia,"['adrenogenital disorder', 'adrenal hyperplasia', 'adrenal hyperplasia, congenital', 'congenital adrenal gland hyperplasia', 'CAH', 'adrenogenital syndrome', 'congenital lipoid adrenal hyperplasia', 'lipoid CAH']",0050811,,418,C0701163,"['-0.661', '0.75', '-0.8867', '-0.1625', '0.1655', '0.1522', '-0.4277', '1.397', '-0.4731', '-0.975', '0.2307', '0.0402', '-0.1696', '2.07', '-0.6196', '0.2764', '-0.1288', '0.503', '-0.4995', '-0.4553', '-0.2054', '-0.001246', '0.3062', '-0.2576', '0.5454', '0.3562', '-0.1119', '-0.163', '1.06', '-0.5', '0.4312', '0.0657', '0.2062', '0.109', '0.0863', '0.732', '-0.178', '0.1396', '-0.1724', '-0.386', '0.1409', '-0.1427', '0.3591', '-0.5503', '0.347', '-1.198', '0.03836', '0.03574', '0.4468', '0.4626', '0.2837', '-0.519', '0.2446', '-0.4622', '0.06128', '0.2091', '-0.02788', '-0.553', '-0.39', '0.311', '-0.2151', '0.415', '0.779', '-0.4905', '0.4653', '0.792', '0.3694', '0.1733', '-0.2834', '0.395', '-0.38', '0.2391', '0.373', '-0.3298', '0.1036', '-0.609', '-0.4055', '-0.4', '-0.219', '-0.424', '0.4568', '0.1515', '0.03766', '-0.7197', '0.4182', '0.1904', '0.146', '-0.6543', '0.5303', '0.2085', '0.003008', '0.4429', '-0.0348', '-0.063', '0.4624', '0.00708', '0.2429', '-0.11633', '-0.01487', '0.408']",C34360,,D000312,255.2,,10010323,
mondo:0018480,"carcinoma of esophagus, salivary gland type","['esophageal carcinoma, salivary gland type']",,,418945,CN237468,,,,,,,,
mondo:0018481,undifferentiated carcinoma of esophagus,"['undifferentiated esophageal carcinoma', 'oesophagus undifferentiated carcinoma', 'esophageal undifferentiated carcinoma', 'esophagus undifferentiated carcinoma', 'undifferentiated esophageal cancer']",,,418951,CN237469,,C27422,,,,,,
mondo:0018483,secondary pulmonary alveolar proteinosis,"['SPAP', 'secondary PAP']",,,420259,C3873302,,,,,,,,
mondo:0018484,semicircular canal dehiscence syndrome,"['Minor^s syndrome', 'canal dehiscence syndrome', 'superior canal dehiscence', 'superior semicircular canal dehiscence syndrome', 'Minorbs syndrome', 'superior canal syndrome', 'superior semicircular canal dehiscence', 'third mobile window syndrome', 'SCD syndrome']",0080193,,420402,,,,,,,,,
mondo:0018485,"glycogen storage disease due to acid maltase deficiency, late-onset","['Pompe disease, late-onset', 'GSD type 2, late onset', 'glycogen storage disease type II, late onset', 'glycogenosis type II, late onset', 'Alpha-1,4-glucosidase acid deficiency, late onset', 'GSD type 2, late-onset', 'Pompe disease, late onset', 'glycogen storage disease type II, late-onset', 'glycogenosis type 2, late-onset', 'Alpha-1,4-glucosidase acid deficiency, late-onset', 'GSD due to acid maltase deficiency, late-onset', 'GSD type II, late onset', 'GSD type II, late-onset', 'glycogen storage disease type 2, late onset', 'GSD due to acid maltase deficiency, late onset', 'glycogen storage disease type 2, late-onset', 'glycogenosis type II, late-onset', 'glycogenosis type 2, late onset']",,,420429,C3888925,,,,,,,,
mondo:0018486,visual snow syndrome,['visual snow'],,,420556,CN237477,,,,,,,,
mondo:0018487,autosomal recessive severe congenital neutropenia due to CXCR2 deficiency,,,,420699,,,,,,,,,
mondo:0018489,autoimmune encephalopathy with parasomnia and obstructive sleep apnea,"['anti-IgLON5 disease', 'anti-IgLON5 syndrome']",,,420789,CN237490,,,,,,,,
mondo:0018490,cono-spondylar dysplasia,['short stature-kyphosis-hypoplasia of basal ilia-cone epiphyses-facial dysmorphism syndrome'],,,420794,CN237491,,,,,,,,
mondo:0018491,3-phosphoglycerate dehydrogenase deficiency,,,,422519,C0580190,,,,,270.7,,,
mondo:0018492,hereditary clear cell renal cell carcinoma,"['hereditary clear cell renal carcinoma', 'Hereditary clear cell renal cell cancer', 'hereditary conventional (clear cell) renal cell carcinoma', 'hereditary conventional renal cell carcinoma', 'hereditary clear cell renal cell carcinoma', 'hereditary clear cell renal cell adenocarcinoma']",7192,,422526,CN237493,,C36260,,,,,,
mondo:0018493,malignant hyperthermia of anesthesia,"['hyperthermia of anaesthesia', 'anaesthesia related hyperthermia', 'malignant hyperpyrexia due to anesthesia', 'malignant hyperthermia syndrome', 'malignant hyperpyrexia due to anaesthesia', 'anesthesia related hyperthermia', 'malignant hyperpyrexia', 'malignant hyperthermia', 'hyperthermia of anesthesia']",8545,,423,C0024591,"['-0.2269', '0.028', '-0.4365', '-0.1243', '0.3037', '-0.519', '0.02954', '0.6133', '0.4595', '-0.332', '0.303', '0.3447', '0.306', '0.152', '-0.796', '0.3184', '-0.3713', '-0.874', '-0.597', '-0.519', '0.358', '0.02689', '0.3484', '-0.5586', '-0.5664', '-0.7334', '-0.01588', '0.2556', '-0.1542', '-0.466', '0.4292', '0.3005', '1.091', '0.03134', '-0.878', '-0.02429', '-0.4119', '0.1765', '0.329', '0.04266', '0.2554', '0.3445', '0.1299', '-0.1716', '0.2151', '-0.01376', '-0.46', '-0.4658', '0.4675', '0.525', '-0.12274', '0.2036', '0.35', '-0.3474', '0.2756', '-0.0488', '0.2109', '0.658', '-0.002903', '-0.4082', '-0.014786', '0.503', '0.3267', '-0.08563', '-0.3337', '0.5474', '0.1885', '0.613', '-0.7656', '0.06058', '-0.2825', '0.2302', '-0.3057', '-0.01576', '-0.0748', '0.674', '1.022', '-0.1798', '0.5', '0.0934', '-0.1526', '-0.0483', '0.544', '0.251', '-0.696', '-0.1442', '0.349', '-0.08026', '0.4583', '0.1731', '0.58', '-0.2195', '-0.09534', '-0.01897', '0.408', '0.0709', '0.0376', '-0.2947', '-0.369', '0.11554']",C84869,,D008305,995.86,,10020844,0002047
mondo:0018494,microcephaly-short stature-intellectual disability-facial dysmorphism syndrome,,,,423306,CN237496,,,,,,,,
mondo:0018495,X-linked intellectual disability-limb spasticity-retinal dystrophy-diabetes insipidus syndrome,,,,423479,CN237501,,,,,,,,
mondo:0018496,ARX-related encephalopathy-brain malformation spectrum,,,,423655,,,,,,,,,
mondo:0018498,double outlet right ventricle with subaortic or doubly committed ventricular septal defect,['DORV with subaortic or doubly committed VSD'],,,423693,,,,,,,,,
mondo:0018499,"double outlet right ventricle with atrioventricular septal defect, pulmonary stenosis, heterotaxy","['DORV with atrioventricular septal defect, pulmonary stenosis, heterotaxy']",,,423712,,,,,,,,,
mondo:0018500,cutaneous larva migrans,"['CLM', 'ground itch', 'dew itch', 'creeping eruption']",,,423717,,,,,D007815,126.9,,,
mondo:0018502,hereditary gastric cancer,"['hereditary cancer of stomach', 'hereditary gastric cancer']",,,423776,,,,,,,,,
mondo:0018503,"carcinoma of stomach, salivary gland type","['gastric carcinoma, salivary gland type']",,,423781,CN237508,,,,,,,,
mondo:0018504,undifferentiated carcinoma of stomach,"['undifferentiated stomach adenocarcinoma', 'stomach undifferentiated carcinoma', 'undifferentiated gastric carcinoma', 'undifferentiated carcinoma of the stomach', 'anaplastic carcinoma of the stomach', 'Gastric undifferentiated carcinoma', 'anaplastic carcinoma of stomach', 'anaplastic gastric carcinoma', 'undifferentiated carcinoma of stomach', 'undifferentiated gastric (stomach) cancer']",,,423786,CN237509,,C5476,,,,,,
mondo:0018506,mesenchymal tumor of small intestine,"['mesenchymal tumor of small bowel', 'mesenchymal tumour of small bowel']",,,423798,CN237511,,,,,,,,
mondo:0018507,microcephaly-complex motor and sensory axonal neuropathy syndrome,,,,423894,CN237512,,,,,,,,
mondo:0018509,squamous cell carcinoma of the small intestine,"['small intestine squamous cell carcinoma', 'squamous cell carcinoma of the small bowel', 'small intestinal squamous cell cancer', 'small intestinal squamous cell carcinoma']",,,423968,CN237514,,C43534,,,,,,
mondo:0018510,small intestine neuroendocrine neoplasm,"['small intestine neuroendocrine tumour', 'small intestine neuroendocrine tumor, well differentiated, low or intermediate grade', 'neuroendocrine tumour of the small intestine', 'neuroendocrine tumour of small bowel', 'small intestinal neuroendocrine neoplasm', 'neuroendocrine neoplasm of the small intestine', 'small intestine neuroendocrine tumor', 'NET of the small intestine', 'small intestine neuroendocrine neoplasm', 'neuroendocrine tumor of small bowel', 'neuroendocrine tumor of the small intestine', 'small intestine NET', 'neuroendocrine neoplasm of small intestine']",4434,,423975,CN237515,,C5803,,,,,,
mondo:0018511,epithelial tumor of the appendix,"['vermiform appendix epithelial neoplasm', 'appendiceal epithelial tumour', 'appendiceal epithelial tumor']",,,423982,CN237516,,,,,,,,
mondo:0018513,squamous cell carcinoma of colon,"['epidermoid carcinoma of the colon', 'colonic epidermoid carcinoma', 'epidermoid carcinoma of colon', 'colon epidermoid carcinoma', 'colon squamous cell carcinoma', 'colonic squamous cell carcinoma', 'squamous cell carcinoma of the colon', 'colon squamous cell cancer', 'squamous cell carcinoma of colon', 'squamous cell colon carcinoma']",5519,,423994,CN237518,,C5490,,,,,,
mondo:0018515,squamous cell carcinoma of rectum,"['rectal squamous cell carcinoma', 'rectum squamous cell carcinoma', 'squamous cell carcinoma of rectum', 'rectal squamous cell cancer', 'squamous carcinoma of rectum', 'rectal squamous carcinoma', 'squamous cell carcinoma of the rectum', 'squamous carcinoma of the rectum']",5528,,424002,C1335690,,C5554,,,,,,
mondo:0018516,epithelial tumor of anal canal,['anal canal epithelial neoplasm'],,,424010,CN237521,,,,,,,,
mondo:0018521,squamous cell carcinoma of pancreas,"['pancreas squamous cell carcinoma', 'squamous cell carcinoma of the pancreas', 'pancreatic squamous cell carcinoma']",0080323,,424039,CN237524,,,,,,,,
mondo:0018523,pancreatic mucinous cystadenoma,"['pancreatic mucinous cystadenocarcinoma', 'pancreas mucinous cystadenoma', 'pancreatic mucinous cystic neoplasm', 'mucinous cystadenoma of pancreas', 'pancreatic colloid cystadenoma', 'mucinous cystadenoma of the pancreas', 'pancreatic colloidal cystadenoma', 'colloidal cystadenoma of the pancreas', 'colloid cystadenoma of pancreas', 'colloidal cystadenoma of pancreas', 'colloid cystadenoma of the pancreas', 'mucinous cystadenocarcinoma of the pancreas', 'pancreatic mucinous cystadenoma']",7735,,424053,,,C5718,,,,,,
mondo:0018525,solid pseudopapillary carcinoma of pancreas,"['pancreatic solid pseudopapillary carcinoma', 'solid pseudopapillary neoplasm of the pancreas', 'solid pseudopapillary carcinoma of pancreas', 'solid pseudopapillary carcinoma of the pancreas']",6827,,424065,C1336029,,C5728,1000542,,,,,
mondo:0018528,congenital myopathy with myasthenic-like onset,,,,424107,,,,,,,,,
mondo:0018529,qualitative or quantitative defects of Torsin-1A-interacting protein 1,['qualitative or quantitative defects of Torsin-1A-interacting protein type 1'],,,424925,,,,,,,,,
mondo:0018531,carcinoma of liver and intrahepatic biliary tract,"['liver/hepatobiliary cancer', 'liver and intrahepatic bile duct carcinoma', 'cancer of the liver and intrahepatic biliary tract', 'cancer of liver', 'liver cancer', 'hepatic cancer', 'cancer of the liver', 'liver carcinoma', 'primary liver carcinoma', 'cancer of liver and intrahepatic biliary tract', 'liver and intrahepatic biliary tract carcinoma', 'hepatocellular carcinoma plus intrahepatic cholangiocarcinoma', 'carcinoma of liver and IBT', 'liver and intrahepatic bile duct cancer', 'carcinoma of liver', 'liver and intrahepatic biliary tract cancer']",,,424936,C0279000,,C7927,,,,C22.1,,
mondo:0018532,adenocarcinoma of liver and intrahepatic biliary tract,"['adenocarcinoma of liver and IBT', 'adenocarcinoma of the liver and IBT', 'adenocarcinoma of the liver and intrahepatic biliary tract']",,,424943,CN242181,,,,,,,,
mondo:0018533,undifferentiated carcinoma of liver and intrahepatic biliary tract,['undifferentiated carcinoma of liver and IBT'],,,424970,CN242153,,,,,,,,
mondo:0018534,squamous cell carcinoma of liver and intrahepatic biliary tract,['squamous cell carcinoma of liver and IBT'],,,424975,CN242131,,,,,,,,
mondo:0018535,biliary cystadenocarcinoma,['intrahepatic bile duct cystadenocarcinoma'],,,424982,C2064409,,,,,,,,
mondo:0018536,adenocarcinoma of gallbladder and extrahepatic biliary tract,"['adenocarcinoma of the gallbladder and extrahepatic biliary tract', 'adenocarcinoma of gallbladder and EBT', 'adenocarcinoma of the gallbladder and EBT']",,,424991,CN237537,,,,,,,,
mondo:0018537,squamous cell carcinoma of gallbladder and extrahepatic biliary tract,['squamous cell carcinoma of gallblader and EBT'],,,424996,CN237538,,,,,,,,
mondo:0018538,inherited digestive cancer-predisposing syndrome,,,,425003,CN237539,,,,,,,,
mondo:0018540,PFAPA syndrome,"['PFAPA', 'periodic fever, aphthous stomatitis, pharyngitis, adenitis syndrome', 'Marshall syndrome with periodic fever', 'Marshall syndrome', 'periodic fever, aphthous stomatitis, pharyngitis and adenitis', 'periodic fever-aphtous stomatitis-pharyngitis-adenopathy syndrome']",,,42642,CN205072,,C116917,,,,,,
mondo:0018541,familial hypoaldosteronism,,,,427,CN205074,"['-0.681', '0.01715', '-0.1407', '-0.1013', '0.04846', '-0.4834', '-0.3306', '0.577', '-0.10333', '-0.164', '0.02313', '-0.227', '-0.206', '0.1583', '-0.3381', '-0.005943', '0.0793', '0.0934', '-0.003073', '-0.7295', '0.3486', '-0.1339', '0.12335', '-0.242', '0.2319', '0.1261', '0.1389', '-0.04413', '-0.04474', '-0.2184', '0.2322', '0.03174', '0.3667', '0.4822', '-0.57', '-0.02658', '0.2031', '0.2192', '-0.4158', '0.02748', '-0.1979', '0.001595', '0.277', '0.0919', '-0.1093', '-0.07446', '-0.2988', '0.0786', '0.222', '0.7583', '0.0797', '-0.249', '-0.1243', '-0.3352', '0.0838', '-0.1499', '0.2415', '-0.375', '-0.1387', '0.3394', '-0.004837', '0.784', '0.4028', '-0.2251', '0.4126', '0.081', '0.4192', '0.02492', '-0.2869', '0.1571', '-0.383', '0.3503', '-0.2045', '-0.3857', '0.0544', '0.0584', '0.1547', '0.2175', '0.04526', '-0.3035', '-0.001914', '0.087', '0.2722', '-0.1581', '0.2808', '0.3655', '0.1868', '-0.418', '0.5537', '-0.08057', '-0.008316', '0.2139', '0.04166', '-0.275', '0.502', '0.689', '0.3062', '-0.587', '0.04977', '-0.1158']",,,,,,,
mondo:0018542,severe congenital neutropenia,"['neutropenia, severe congenital', 'SCN']",0050590,,42738,,"['0.3347', '0.06464', '-0.8438', '-0.4153', '0.367', '-0.00783', '0.413', '0.9556', '-0.353', '-0.556', '-0.12463', '0.0799', '0.02194', '0.02829', '0.05914', '-0.07416', '0.1947', '-0.194', '0.1704', '-0.5293', '-0.1569', '-0.2037', '0.3838', '-0.398', '0.00956', '0.134', '-0.4084', '0.316', '-0.355', '-0.1332', '0.10803', '0.1481', '0.1815', '0.3848', '-0.595', '0.3496', '-0.3247', '-0.6646', '-0.3584', '0.10394', '-0.2039', '0.2942', '0.0573', '-0.6294', '-0.2477', '0.007614', '-0.584', '0.0477', '0.0712', '0.12085', '0.1747', '-0.2013', '0.628', '0.05362', '-0.1537', '0.1929', '0.2664', '-0.007526', '-0.04773', '-0.1296', '-0.1409', '0.5635', '0.1195', '-0.1908', '0.4673', '-0.3179', '0.262', '-0.05084', '-0.466', '0.369', '-0.078', '-0.4478', '-0.336', '-0.5586', '0.3323', '-0.003592', '0.5625', '0.0298', '0.3765', '-0.399', '-0.5757', '0.1626', '0.282', '0.1403', '-0.2245', '0.1552', '0.03275', '0.351', '-0.352', '0.3564', '0.2559', '0.03592', '0.0364', '0.1578', '0.4993', '0.7124', '0.5874', '-0.766', '-0.5977', '0.01543']",C166152,,,288.01,,10052210,
mondo:0018543,autosomal dominant hypocalcemia,"['hypocalcemia, autosomal dominant', 'AD hypocalcemia', 'hypocalcemia']",0090109,,428,CN205077,"['0.3606', '0.3018', '0.2593', '0.0718', '-0.2905', '0.3364', '-0.2437', '1.282', '-0.3748', '-0.4172', '-0.2947', '0.11365', '0.04376', '0.6646', '0.01607', '-0.0717', '-0.1245', '-0.1864', '0.1934', '-0.651', '0.3071', '-0.431', '0.818', '-0.11536', '0.7173', '0.598', '-0.184', '-0.0011215', '0.2595', '-0.09265', '-0.01251', '-0.0225', '-0.087', '-0.36', '-0.944', '-0.2944', '-0.3374', '0.1776', '-0.2274', '-0.1509', '0.4238', '-0.2993', '0.578', '-0.785', '0.5254', '-0.7207', '0.3208', '-0.8765', '0.02849', '0.4365', '0.03955', '-0.02678', '0.1725', '-0.5405', '0.05338', '0.1589', '0.3667', '-0.4937', '-0.4663', '0.611', '0.2064', '0.403', '-0.1237', '-0.3025', '0.2998', '0.2524', '0.3052', '1.008', '-0.2961', '0.0547', '0.2656', '-0.4265', '0.111', '0.1073', '0.515', '0.4612', '-0.224', '-0.10443', '0.1755', '0.1049', '0.3813', '0.337', '0.1488', '0.4326', '0.09076', '0.4734', '-0.1577', '-0.1569', '0.3726', '0.4883', '0.185', '0.396', '-0.46', '-0.3132', '0.4587', '0.234', '-0.03464', '-0.5444', '-0.7715', '0.2034']",,,,,,,
mondo:0018544,adrenoleukodystrophy,"['adrenomyeloneuropathy, adult, X-linked recessive', 'Siemerling-Creutzfeldt disease', 'adrenoleukodystrophy, X-linked recessive', 'sudanophilic cerebral sclerosis', 'encephalitis periaxialis, Schilder^s', 'X-ALD', 'encephalitis periaxialis concentrica', 'adrenomyeloneuropathy, adult', 'diffuse sclerosis', 'ALD', 'X-linked adrenoleukodystrophy', 'ABCD1 deficiency', 'diffuse cerebral sclerosis of Schilder', 'adrenoleukodystrophy', 'adrenoleukodystrophy, X-linked', 'Bronze-Schilder disease', 'X-linked ALD']",10588,300100,43,C0007795,"['-0.46', '0.4844', '-0.08093', '-0.727', '-0.0849', '-0.1378', '0.00852', '1.029', '-0.7373', '-0.3428', '-0.12256', '-0.1021', '-0.4246', '0.375', '0.6357', '-0.8066', '0.04776', '0.406', '-0.2246', '-0.684', '-0.1842', '-0.4993', '0.2585', '-0.822', '-0.10065', '0.0794', '-0.2693', '-0.02858', '-0.3628', '-0.3042', '0.585', '0.1908', '1.021', '-0.1107', '-0.3384', '-0.2546', '-0.718', '-0.2401', '-0.745', '0.2905', '0.2357', '0.0896', '0.541', '-0.591', '-0.177', '-0.02962', '-0.4324', '-0.0511', '-0.08734', '0.547', '0.603', '0.4668', '-0.642', '-0.408', '0.156', '0.194', '1.397', '-0.3337', '0.01561', '0.6323', '0.1015', '0.1403', '0.765', '0.229', '-0.1896', '0.1439', '0.1412', '0.686', '-0.1414', '0.2363', '0.0538', '0.2869', '-0.2025', '-0.6035', '0.909', '0.007553', '-0.11273', '0.573', '-0.5195', '-0.2563', '-0.2612', '-0.3523', '0.7046', '0.1692', '0.2725', '0.1646', '0.10596', '-0.3132', '0.607', '-1.045', '0.1675', '0.05728', '0.1779', '-0.06064', '0.626', '-0.08514', '0.2021', '-0.2175', '0.1371', '-0.314']",C61252,,D000326,341.1,,10051260,
mondo:0018546,serotonin syndrome,"['serotonin storm', 'serotonergic syndrome', 'serotonin toxidrome', 'serotonin toxicity']",,,43116,,,,1001842,D020230,333.99,,10040108,
mondo:0018547,acute tricyclic antidepressant poisoning,,,,43117,CN227537,,,,,,,,
mondo:0018548,acute poisoning by drugs with membrane-stabilizing effect,,,,43119,CN227538,,,,,,,,
mondo:0018550,spastic paraplegia-optic atrophy-neuropathy and spastic paraplegia-optic atrophy-neuropathy-related disorder,['SPOAN and SPOAN-related disorder'],,,431320,CN237550,,,,,,,,
mondo:0018551,patent urachus,"['patent urachus', 'patent urachus (disease)']",,,431341,CN237552,,C99005,,,,,,0010479
mondo:0018552,urachal sinus,,,,431344,CN237553,,,,,,,,
mondo:0018553,urachal diverticulum,['Vesicourachal diverticulum'],,,431347,CN237554,,C123254,,,,,,
mondo:0018554,pulmonary veno-occlusive disease and/or pulmonary capillary haemangiomatosis,['PVOD and/or PCH'],,,431353,CN237555,,,0009199,,,,,
mondo:0018555,hypogonadotropic hypogonadism,"['gonadotropic deficiency', 'nIHH', 'secondary hypogonadism', 'isolated congenital gonadotropin deficiency', 'normosmic congenital hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism', 'congenital idiopathic hypogonadotropic hypogonadism', 'Normosmic idiopathic hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism with or without anosmia', 'central hypogonadism', 'hypogonadotropism']",7455,,432,CN235466,"['-0.4043', '0.0031', '0.2256', '-0.1768', '0.2163', '-0.206', '-0.00755', '0.1644', '-0.1121', '-0.2688', '-0.04996', '-0.0006785', '-0.0853', '0.04736', '0.0286', '-0.1814', '0.089', '0.08685', '-0.2133', '-0.4666', '-0.08984', '-0.1161', '0.005203', '-0.2413', '0.10565', '0.0447', '0.01498', '-0.1497', '0.1362', '-0.4243', '0.3262', '0.1407', '0.3354', '-0.02823', '-0.2217', '-0.06836', '0.12146', '-0.0786', '0.03195', '-0.272', '0.3164', '0.0793', '0.005127', '0.01185', '0.06036', '-0.364', '0.0842', '-0.134', '0.003443', '0.2793', '0.05573', '-0.00547', '-0.1175', '0.0717', '-0.1278', '-0.011696', '0.4336', '-0.1489', '-0.3193', '0.1652', '0.2496', '0.1578', '0.1305', '0.08264', '-0.01191', '0.12476', '0.2769', '0.2136', '-0.1823', '0.0568', '-0.4216', '0.08044', '0.07623', '-0.2527', '0.2688', '-0.246', '0.1729', '-0.01292', '-0.2979', '-0.1058', '0.001291', '0.07367', '0.0678', '0.07886', '-0.0634', '0.02097', '0.1748', '-0.03812', '0.0462', '-0.009224', '-0.06964', '0.4524', '-0.03055', '-0.0772', '0.5034', '-0.02016', '0.2332', '-0.2283', '0.01058', '0.2703']",C113347,,,253.4,E23.0,,0000044
mondo:0018556,Lambert-Eaton myasthenic syndrome,"['myasthenic syndrome of Lambert-Eaton', 'Lambert Eaton myasthenic syndrome', 'Lambert-Eaton syndrome', 'myasthenic-myopathic syndrome of Lambert-Eaton', 'Eaton-Lambert syndrome', 'Lambert Eaton syndrome', 'LEMS', 'Eaton Lambert syndrome']",0050214,,43393,C0022972,,C3155,,D015624,358.3,,10067685,
mondo:0018559,fetal lower urinary tract obstruction,['LUTO'],,,435365,C4305545,"['-0.0757', '0.0533', '0.03093', '-0.094', '-0.01372', '-0.08514', '0.03763', '0.185', '-0.154', '-0.02003', '-0.05743', '-0.0866', '-0.0452', '0.0879', '-0.12445', '-0.0834', '-0.03412', '-0.0352', '-0.0711', '-0.2201', '-0.02911', '-0.0846', '0.0909', '-0.0774', '0.06586', '-0.03882', '-0.000479', '0.1096', '-0.00371', '-0.02428', '0.11066', '-0.04544', '0.0599', '0.0773', '-0.02101', '-0.00901', '-0.05057', '0.0241', '-0.013794', '-0.10223', '-0.00637', '-0.0644', '0.0767', '0.001807', '0.00716', '-0.0872', '-0.0297', '0.05322', '0.03087', '0.11017', '-0.1184', '0.00901', '0.014015', '-0.05057', '-0.0883', '-0.01991', '0.083', '-0.1376', '-0.1663', '0.00944', '0.11444', '0.07', '-0.06256', '0.0768', '0.02013', '-0.02112', '0.1763', '0.09515', '-0.0966', '0.1361', '-0.07806', '0.05115', '0.04764', '-0.0253', '-0.04477', '0.0525', '0.07367', '-0.009605', '-0.06476', '-0.06207', '-0.0959', '-0.0242', '0.0665', '0.1483', '0.00296', '0.02187', '0.0439', '0.03177', '0.153', '-0.06915', '0.02284', '0.10297', '-0.035', '0.0407', '0.2783', '0.09784', '0.1038', '-0.1543', '-0.05923', '0.09534']",,,,,,,
mondo:0018561,precocious puberty in female,['female organism precocious puberty'],,,435561,C0271616,,,,,,,,0010465
mondo:0018562,hereditary otorhinolaryngological malformation,['genetic otorhinolaryngological malformation'],,,435603,,,,,,,,,
mondo:0018563,adactyly of foot,['congenital absence of toes'],,,435623,,,,,,,,,
mondo:0018564,3p25.3 microdeletion syndrome,"['Del(3)p(25.3)', 'monosomy 3p25.3', 'intellectual disability-epilepsy-stereotypic hand movement syndrome']",,,435638,CN237571,,,,,,,,
mondo:0018565,congenital urachal anomaly,,,,435743,,,,,,,,,
mondo:0018566,short stature-advanced bone age-early-onset osteoarthritis syndrome,,,,435804,CN237575,,,,,,,,
mondo:0018567,autosomal dominant Charcot-Marie-Tooth disease type 2 due to TFG mutation,['CMT2 due to TFG mutation'],,,435819,CN237576,,,,,,,,
mondo:0018569,X-linked microcephaly-growth retardation-prognathism-cryptorchidism syndrome,,,,435938,CN237580,,,,,,,,
mondo:0018570,hypophosphatasia,"['HPP', 'Rathburn disease', 'childhood hypophosphatasia', 'deficiency of alkaline phosphatase (disorder) [ambiguous]', 'hypophospatasia, childhood', 'phosphoethanolaminuria', 'deficiency of alkaline phosphatase', 'phosphoethanol-aminuria', 'hypophosphatasia mild']",14213,,436,C0020630,"['-0.3152', '-0.436', '0.04385', '-0.1725', '0.1235', '-0.3357', '0.0969', '1.535', '-0.1382', '0.4517', '-0.75', '0.0843', '-0.234', '0.718', '0.001778', '0.3857', '0.121', '0.10077', '-0.754', '-0.733', '-0.2074', '-0.562', '0.9966', '-0.4285', '-0.06186', '-0.163', '0.4514', '-0.1165', '0.02277', '-0.678', '0.0734', '0.294', '-0.1482', '0.5376', '0.0669', '-0.02019', '-0.1605', '-0.351', '0.445', '0.0881', '0.4504', '-0.728', '0.3022', '-0.6123', '0.2206', '-0.458', '-0.036', '-0.152', '0.2035', '0.1312', '0.122', '-0.615', '-0.1647', '-0.1683', '0.02005', '-0.6387', '-0.0434', '-0.3506', '0.2295', '-0.1425', '0.254', '-0.427', '0.02269', '-0.4612', '0.04718', '0.335', '0.4478', '0.2162', '-0.2482', '0.04135', '0.1914', '-0.12274', '0.4082', '-0.52', '0.677', '0.02551', '0.2235', '0.3', '0.5093', '-0.8057', '-0.622', '0.06415', '-0.1144', '0.595', '0.4463', '0.6885', '0.2942', '-0.4146', '0.1356', '-0.289', '0.2446', '0.01645', '-0.3638', '-0.1686', '0.1475', '0.4834', '1.08', '-0.593', '-0.3145', '-0.4563']",C26798,,D007014,277.6,E83.3,10049933,
mondo:0018571,contractures-developmental delay-Pierre Robin syndrome,['5q23 microdeletion syndrome'],,,436003,CN237584,,,,,,,,
mondo:0018572,severe intellectual disability-hypotonia-strabismus-coarse face-planovalgus syndrome,,,,436141,CN237585,,,,,,,,
mondo:0018573,intrauterine growth restriction-short stature-early adult-onset diabetes syndrome,,,,436144,CN237586,,,,,,,,
mondo:0018574,intellectual disability-expressive aphasia-facial dysmorphism syndrome,['intellectual disability-loss of expressive language-facial dysmorphism syndrome'],,,436151,CN237587,,,,,,,,
mondo:0018575,microcephalic primordial dwarfism-insulin resistance syndrome,,,,436182,CN237592,,,,,,,,
mondo:0018576,non-progressive predominantly posterior cavitating leukoencephalopathy with peripheral neuropathy,,,,436271,,,,,,,,,
mondo:0018577,pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa,['PXE-like syndrome with retinitis pigmentosa'],,,436274,CN237597,,,,,,,,
mondo:0018579,disorder of ketone body transport,['disorder of keton body transport'],,,438072,CN237600,,,,,,,,
mondo:0018580,PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome,,,,438213,CN237608,,,,,,,,
mondo:0018581,progressive encephalomyelitis with rigidity and myoclonus,['perm'],,,438266,C1861457,,,,,,,,
mondo:0018582,GCGR-related hyperglucagonemia,"['nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumour', 'MVAH', 'nesidioblastosis alpha cell hyperplasia microglucagonoma and nonfunctioning islet cell tumour', 'nesidioblastosis alpha cell hyperplasia microglucagonoma and nonfunctioning islet cell tumor', 'nesidioblastosis, alpha cell hyperplasia, microglucagonoma, and nonfunctioning islet cell tumor', 'Mahvash disease', 'alpha-cell hyperplasia with glucagonemia']",0112306,619290,438274,CN237611,,,,,,,,
mondo:0018583,human infection by orthopoxvirus,,,,438279,CN237612,,,,,,,,
mondo:0018585,pediatric arterial ischemic stroke,"['pediatric AIS', 'childhood arterial ischaemic stroke', 'childhood AIS', 'paediatric AIS', 'childhood arterial ischemic stroke']",,,439175,,,,,,,,,
mondo:0018586,zinc-responsive necrolytic acral erythema,"['necrolytic acral erythema', 'NAE']",,,439196,CN237615,,,,,,,,
mondo:0018587,non-recovering obstetric brachial plexus lesion,"['chronic obstetric brachial plexus palsy', 'non-recovering OBPL', 'chronic obstetric brachial plexus injury', 'non-recovering OBPI']",,,439202,CN237616,,,,,,,,
mondo:0018588,ALECT2 amyloidosis,"['LECT2 amyloidosis', 'leukocyte chemotactic factor-2 amyloidosis']",,,439224,,,,,,,,,
mondo:0018589,AApoAIV amyloidosis,['apolipoprotein A-IV amyloidosis'],0080927,,439232,,,,,,,,,
mondo:0018590,ABeta2M amyloidosis,['Beta2-microglobulinic amyloidosis'],0080928,,439246,,,,,,,,,
mondo:0018591,ITM2B amyloidosis,"['ITM2B-related amyloidosis', 'ITM2B-related cerebral amyloid angiopathy', 'familial cerebral amyloid angiopathy']",,,439254,CN237622,,,,,277.39,,,
mondo:0018592,cutaneous polyarteritis nodosa,"['cutaneous periarteritis nodosa', 'cutaneous PAN']",,,439729,CN242143,,C117295,,,709.8,,,
mondo:0018593,primary polyarteritis nodosa,"['primary periarteritis nodosa', 'primary PAN']",,,439737,CN237623,,,,,,,,
mondo:0018594,secondary polyarteritis nodosa,"['secondary periarteritis nodosa', 'secondary PAN', 'Scondary PAN']",,,439746,CN237624,,,,,,,,
mondo:0018595,single-organ polyarteritis nodosa,"['single-organ PAN', 'single-organ periarteritis nodosa']",,,439755,CN242112,,,,,,,,
mondo:0018596,systemic polyarteritis nodosa,"['systemic PAN', 'systemic periarteritis nodosa']",,,439762,CN242146,,,,,,,,
mondo:0018597,plastic bronchitis,"['pseudo-membranous bronchitis', 'fibrinous bronchitis', 'croupous bronchitis']",,,439881,C0264342,,,,,,,,
mondo:0018599,congenital oculomotor nerve palsy,"['congenital third cranial nerve palsy', 'congenital CNIII lesion']",,,440221,,,,,,,,,
mondo:0018600,congenital abducens nerve palsy,"['congenital CNVI palsy', 'benign congenital sixth cranial nerve palsy']",,,440233,,,,,,,,,
mondo:0018601,autosomal dominant myopia-midfacial retrusion-sensorineural hearing loss-rhizomelic dysplasia syndrome,,,,440354,CN237631,,,,,,,,
mondo:0018602,necrotizing soft tissue infection,['NSTI'],,,440368,CN237632,,,,,729.99,M72.6,,
mondo:0018603,interstitial lung disease due to SP-C deficiency,['interstitial lung disease due to surfactant protein C deficiency'],,,440392,CN237633,,,,,,,,
mondo:0018604,familial colorectal cancer type X,"['FCCTX', 'familial colorectal cancer type X']",,,440437,CN237636,,C120084,,,,,,
mondo:0018605,disorders of pentose/polyol metabolism,,,,440701,CN237637,,,,,,,,
mondo:0018606,extensive peripapillary myelinated nerve fibers,,,,440724,CN237640,,,,,,,,
mondo:0018607,combined hamartoma of the retina and retinal pigment epithelium,"['CHR-RPE', 'combined hamartoma of the retina and RPE']",,,440727,CN237641,,C174548,,,,,,
mondo:0018608,pure autonomic failure,"['Bradbury-Eggleston syndrome', 'Pure dysautonomia', 'orthostatic hypotension (a symptom)', 'PAF', 'idiopathic orthostatic hypotension', 'idiopathic orthostatic hypotension (a symptom)', 'Pure idiopatic dysautonomia', 'Bradbury Eggleston syndrome']",,,441,CN205091,,,,D054970,,,,
mondo:0018610,early-onset posterior subcapsular cataract,,,,441447,CN237646,,,,,,,,
mondo:0018611,early-onset lamellar cataract,,,,441452,CN237647,,,,,,,,
mondo:0018612,congenital hypothyroidism,"['congenital hypothyroidism', 'congenital goitre', 'foetal iodine deficiency syndrome', 'cretinism']",0050328,,442,C0010308,,C26734,,D003409,759.89,,10010510,
mondo:0018613,AH amyloidosis,['heavy chain amyloidosis'],0080934,,442582,,,C158962,,,,,,
mondo:0018614,undetermined early-onset epileptic encephalopathy,['undetermined EOEE'],,,442835,,,,,,,,,
mondo:0018615,hemicrania continua,,,,443070,CN237652,,,,,339.41,G44.51,,
mondo:0018616,central serous chorioretinopathy,"['CSC', 'CSCR', 'central serous retinopathy', 'central serous choroidopathy', 'central serous chorioretinopathy after bone marrow transplantation']",,,443079,C0730328,,C115124,,D056833,362.41,,,
mondo:0018617,baroreflex failure,,,,443084,CN237655,,,,,,,,
mondo:0018620,hypothalamic adipsic hypernatraemia syndrome,,,,443101,CN237660,,,,,,,,
mondo:0018621,lymphoplasmacytic lymphoma without IgM production,['lymphoplasmacytic lymphoma without Immunoglobulin M production'],,,443159,,,,,,,,,
mondo:0018623,postpartum psychosis,['puerperal psychosis'],,,443173,,,,,,648.44,F53,,
mondo:0018624,spontaneous intracranial hypotension,['spontaneous cerebrospinal fluid leak'],,,443180,CN237665,,,,,,,,
mondo:0018625,classic stiff person syndrome,['classic SPS'],,,443192,CN237666,,,,,,,,
mondo:0018626,paratyphoid fever,"['paratyphoid B fever', 'paratyphoid A fever', 'paratyphoid fever B', 'paratyphoid b', 'paratyphoid a', 'paratyphoid', 'paratyphoid C fever', 'paratyphoid fever A', 'paratyphoid fever C', 'paratyphoid c']",3055,,443227,C0343377,,C34897,0007420,D010284,002.9,,,
mondo:0018628,HIV-associated cancer,['HIV-related cancer'],,,443291,CN237671,,,,,,,,
mondo:0018629,focal stiff limb syndrome,"['focal stiff-person syndrome', 'Stiff leg syndrome']",,,443804,CN237672,,,,,,,,
mondo:0018630,hereditary nonpolyposis colon cancer,"['hereditary nonpolyposis colon cancer', 'hereditary nonpolyposis colorectal cancer', 'familial nonpolyposis colon cancer', 'HNPCC', 'familial nonpolyposis colorectal cancer', 'Hereditary nonpolyposis colorectal cancer (HNPCC)', 'colorectal cancer, hereditary nonpolyposis']",,,443909,CN237674,,C120083,,,,,,
mondo:0018631,Marie Unna hereditary hypotrichosis,"['hypotrichosis caused by mutation in HR', 'Marie Unna congenital hypotrichosis', 'MUHH', 'hypotrichosis, Marie Unna type', 'HR hypotrichosis']",,,444,C2931059,"['-0.1261', '0.10956', '-0.11444', '-0.2822', '0.587', '-0.6924', '-0.3916', '0.9004', '-0.386', '-0.2854', '0.07874', '0.3818', '-0.416', '0.05548', '0.1416', '0.1946', '0.7324', '-0.3015', '-0.3767', '-0.6978', '-0.565', '-0.8994', '0.445', '-0.4868', '0.575', '0.1425', '-0.3706', '-0.1919', '-0.022', '-0.4338', '0.6416', '-0.01672', '-0.1261', '0.2998', '0.23', '0.0741', '-0.00358', '-0.2141', '0.0883', '0.3708', '0.1744', '0.1698', '-0.145', '-0.2893', '0.4187', '-0.6084', '-0.08655', '0.376', '0.000455', '-0.1687', '0.3389', '-0.1356', '0.6157', '-0.3242', '-0.03406', '-0.2532', '0.845', '-0.579', '-0.2898', '-0.79', '-0.3762', '0.0967', '0.6665', '-0.2396', '0.05933', '0.11096', '0.4775', '0.303', '-0.1351', '0.5864', '0.02754', '-0.2047', '0.0733', '-0.1704', '0.04932', '-0.1691', '-0.1852', '0.4587', '-0.1569', '-0.02591', '0.5376', '-0.2251', '0.596', '0.1644', '0.405', '-0.2373', '-0.3154', '-0.1622', '0.261', '0.5566', '0.093', '0.6855', '0.59', '0.2766', '0.606', '-0.4224', '0.3242', '-0.4841', '0.33', '0.0981']",,,C535912,,,,
mondo:0018632,11q22.2q22.3 microdeletion syndrome,"['Del(11)(q22.2q22.3)', 'monosomy 11q22.2q22.3', 'monosomy 11q22.2-q22.3', '11q22.2-q22.3 deletion syndrome']",,,444002,CN237678,,,,,,,,
mondo:0018633,20q11.2 microdeletion syndrome,"['monosomy 20q11', 'Del(20)(q11.2)']",,,444051,CN237681,,,,,,,,
mondo:0018634,hereditary amyloidosis,"['hereditary amyloidosis (disease)', 'amyloidosis, Familial', 'familial amyloidosis', 'amyloidosis hereditary']",,,444116,C0206246,,C84555,,D028226,,,,
mondo:0018635,idiopathic phalangeal acro-osteolysis,['idiopathic phalangeal acroosteolysis'],,,444316,,,,,,,,,
mondo:0018636,autoimmune hemolytic anemia-autoimmune thrombocytopenia-primary immunodeficiency syndrome,"['TPPII-related immunodeficiency, autoimmunity, and neurodevelopmental delay with impaired glycolysis and lysosomal expansion disease', 'tripeptidyl-peptidase II deficiency', 'TPPII deficiency', 'triangle disease', 'Evans syndrome associated with primary immunodeficiency']",,,444463,CN237691,,,,,,D61.0,,
mondo:0018637,familial chylomicronemia syndrome,,0111417,,444490,CN231410,,,,,,,,
mondo:0018638,pseudohypoaldosteronism,,4479,,444916,C0033805,,C85034,,D011546,255.8,,,
mondo:0018639,caudal regression-sirenomelia spectrum,,,,444941,,,,,,,,,
mondo:0018640,secondary vasculitis,,,,445197,,,,,,,,,
mondo:0018642,NIK deficiency,"['primary immunodeficiency with multifaceted aberrant lymphoid immunity', 'non-severe combined immunodeficiency caused by mutation in MAP3K14', 'MAP3K14 non-severe combined immunodeficiency']",,,447731,,,,,,,,,
mondo:0018643,susceptibility to localized juvenile periodontitis,,,,447740,,,,,,,,,
mondo:0018644,autosomal dominant complex spastic paraplegia type 9B,['AD-SPG9B'],,,447757,CN237702,,,,,,,,
mondo:0018645,IgG4-related sclerosing cholangitis,,,,447764,C4302109,,,,,,,,
mondo:0018646,sclerosing cholangitis,"['sclerosing cholangitis', 'primary sclerosing cholangitis (PSC)', 'sclerosing cholangitis (disease)', 'Primary sclerosing cholangitis', 'fibrosing cholangitis']",14268,,447771,C0008313,"['-0.11957', '0.0834', '-0.001519', '-0.3013', '0.003649', '-0.2294', '0.0665', '0.012115', '0.03174', '0.249', '0.01148', '-0.2349', '-0.1875', '0.3035', '-0.4458', '-0.533', '-0.1846', '-0.04437', '0.035', '-0.544', '-0.04004', '-0.3057', '0.3481', '-0.2896', '0.0698', '-0.2263', '0.1005', '0.43', '0.1923', '-0.1315', '0.11206', '-0.1373', '0.2198', '0.2267', '0.1279', '-0.2186', '-0.4768', '0.10345', '0.0769', '-0.0663', '-0.2607', '0.1886', '0.2834', '0.2382', '0.0814', '-0.08154', '-0.04205', '-0.0381', '-0.0575', '0.11285', '-0.1719', '0.2688', '0.2421', '0.17', '-0.00507', '-0.2457', '-0.05475', '-0.1448', '-0.53', '-0.22', '0.2256', '0.249', '-0.004013', '-0.2256', '0.1487', '-0.04584', '0.513', '0.4102', '-0.3699', '0.366', '-0.4155', '-0.1247', '0.1948', '-0.111', '-0.1786', '0.04987', '0.2502', '0.2175', '0.1345', '-0.05222', '-0.3293', '-0.1228', '-0.3582', '-0.4465', '-0.0759', '-0.1587', '0.2076', '-0.01432', '0.209', '-0.121', '0.1564', '0.0833', '-0.1273', '0.212', '0.712', '0.1611', '0.04413', '-0.1652', '0.00387', '-0.04465']",C4828,0004268,,,,,0030991
mondo:0018647,secondary sclerosing cholangitis,,,,447774,C0400978,,,,,,,,
mondo:0018648,Keratocystic odontogenic tumor,"['odontogenic Keratocyst', 'KTOC', 'odontogenic keratocystoma']",,,447777,CN237705,,C54302,,,,,,
mondo:0018653,Polymerase proofreading-related adenomatous polyposis,['PPAP'],,,447877,,,C162484,,,,,,
mondo:0018654,idiopathic dropped head syndrome,['isolated neck extensor myopathy'],,,447881,CN237712,,,,,,,,
mondo:0018655,hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome,,,,447893,CN237713,,,,,,,,
mondo:0018656,tremor-ataxia-central hypomyelination syndrome,['TACH syndrome'],,,447896,CN237714,,,,,,,,
mondo:0018657,pigmentation defects-palmoplantar keratoderma-skin carcinoma syndrome,"['CANCER, ALOPECIA, PIGMENT DYSCRASIA, ONYCHODYSTROPHY, AND KERATODERMA', 'CAPOK']",,618373,447961,CN237716,,,,,,,,
mondo:0018658,19p13.3 microduplication syndrome,['dup(19)(p13.13)'],,,447980,CN237720,,,,,,,,
mondo:0018659,partial duplication of the short arm of chromosome 19,"['partial duplication of the short arm of chromosome type 19', 'partial trisomy of chromosome 19p', 'partial trisomy of the short arm of chromosome 19', 'partial duplication of chromosome 19p']",,,447985,,,,,,,,,
mondo:0018660,hemophilia,,,,448,C0684275,,C3093,,,,,10061992,
mondo:0018661,Zika virus infectious disease,"['ZikV infection', 'Zika', 'Zika fever', 'fever, Zika', 'Zika virus caused disease or disorder', 'congenital Zika syndrome', 'Zika virus disease', 'Zika virus infection', 'congenital Zika virus infection']",0060478,,448237,CN237724,,C128423,,D000071243,,A92.5,,
mondo:0018662,autosomal recessive brachyolmia,"['brachyolmia, autosomal recessive', 'brachyolmia, Hobaek/Toledo type']",,,448242,CN237725,,,,,,,,
mondo:0018663,regressive spondylometaphyseal dysplasia,['Pelger-Huet anomaly with mild skeletal anomalies'],,618019,448267,CN248525,"['-0.629', '0.1707', '0.1991', '-0.3396', '0.12024', '-0.04453', '0.0953', '0.412', '-0.3694', '-0.1887', '-0.2268', '0.157', '0.06586', '-0.0644', '-0.1388', '0.09', '0.2306', '-0.03625', '-0.05194', '-0.3262', '-0.06335', '0.05536', '0.4204', '-0.0294', '0.2017', '0.1658', '-0.1616', '-0.1785', '0.0769', '0.12396', '-0.0201', '-0.0675', '0.1787', '0.1619', '0.3508', '-0.1783', '-0.03784', '-0.4016', '0.03029', '-0.5', '-0.0756', '-0.413', '-0.07556', '-0.1725', '-0.0646', '-0.365', '-0.11334', '0.502', '0.2258', '-0.09283', '0.0903', '0.05524', '-0.01156', '0.002663', '-0.4575', '-0.6147', '-0.01678', '-0.2937', '-0.1179', '-0.04782', '0.3389', '0.0632', '-0.563', '0.03024', '-0.013466', '-0.147', '0.1764', '0.2177', '-0.1381', '0.12213', '-0.2593', '-0.07745', '0.1549', '-0.1337', '-0.0923', '0.0501', '-0.03824', '-0.04578', '-0.11847', '-0.2842', '0.11224', '-0.009834', '0.06726', '0.2432', '-0.253', '0.09106', '-0.0633', '0.3406', '0.3113', '0.0865', '-0.0601', '0.02222', '0.08936', '0.292', '0.3906', '0.0646', '0.507', '-0.453', '0.3098', '0.2842']",,,,,,,
mondo:0018664,ectopia cordis,"['ectopia cordis', 'ectopia cordis (disease)']",,,448270,,,C111643,,D054083,746.87,,,0001683
mondo:0018665,X-linked acrogigantism due to a point mutation,"['X-LAG (X-linked acrogigantism) due to a point mutation', 'familial infantile gigantism due to a point mutation']",,,448348,CN237730,,,,,,,,
mondo:0018666,hepatoblastoma,"['hepatoblastoma, malignant', 'hepatoblastoma', 'pediatric hepatoblastoma', 'pediatric embryonal hepatoma', 'paediatric embryonal hepatoma', 'HBL', 'paediatric hepatoblastoma']",687,,449,C0206624,,C3728,1000292,D018197,,,10062001,
mondo:0018667,pleural empyema,"['pleural empyema', 'abscess of pleural cavity', 'empyema', 'pyothorax', 'empyema of pleura', 'thorax abscess', 'purulent pleurisy', 'purulent pleuritis', 'pleural empyema (disease)', 'abscess of thorax']",3798,,449266,,,,,D016724,,,,0011919
mondo:0018668,scedosporiosis,,,,449280,,,,,C000656924,,,,
mondo:0018669,snakebite envenomation,,,,449285,CN237735,,,,,,,,
mondo:0018670,symptomatic form of fragile X syndrome in female carrier,,,,449291,CN237736,,,,,,,,
mondo:0018671,IgG4-related kidney disease,,,,449395,CN237737,,,,,,,,
mondo:0018672,IgG4-related aortitis,['IgG4-related periaortitis'],,,449400,,,,,,,,,
mondo:0018673,IgG4-related pachymeningitis,"['idiopathic hypertrophic pachymeningitis', 'idiopathic hypertrophic spinal pachymeningitis', 'idiopathic hypertrophic craniospinal pachymeningitis', 'idiopathic hypertrophic cranial pachymeningitis']",,,449427,C4545992,,,,,,,,
mondo:0018674,IgG4-related submandibular gland disease,"['Kuttner tumor', 'Kuttner tumour', 'Kuttner^s tumor', 'Küttner tumour', 'chronic sclerosing sialadenitis', 'Küttner tumor', 'IgG4-related sialadenitis', 'Kuttner^s tumour']",,,449432,,,C82887,,,,,,
mondo:0018675,IgG4-related ophthalmic disorder,['eye IgG4-related disease'],,,449563,CN237741,,,,,,,,
mondo:0018676,eosinophilic angiocentric fibrosis,"['Sinonasal eosinophilic angiocentric fibrosis', 'IgG4-related eosinophilic angiocentric fibrosis', 'eosinophilic angiocentric fibrosis', 'EAF']",,,449566,,,,,,,,,
mondo:0018677,visceral heterotaxy,"['heterotaxia', 'lateralization defect', 'incomplete situs inversus', 'visceral heterotaxy', 'heterotaxia syndrome', 'heterotaxy syndrome', 'situs ambiguus', 'situs ambiguous', 'partial situs inversus', 'heterotaxy, visceral']",0050545,,450,C3178805,,C117273,0009081,,,,10067265,
mondo:0018678,polyclonal hyperviscosity syndrome,,,,450322,CN237743,,,,,,D89.0,,
mondo:0018679,primary cutaneous plasmacytosis,,,,451602,,,,,,,,,
mondo:0018680,cutaneous pseudolymphoma,"['lymphadenosis Benigna cutis', 'pseudolymphoma of Spiegler', 'lymphocytoma cutis']",,,451607,C0311220,,C62776,,,,,,
mondo:0018681,neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome,,,,453499,CN237747,,,,,,,,
mondo:0018682,congenital insensitivity to pain with severe intellectual disability,"['congenital analgesia with severe intellectual disability', 'congenital absence of pain with severe intellectual disability', 'congenital insensitivity to pain with preserved temperature sensation', 'congenital insensitivity to pain with severe non-progressive cognitive delay']",,,453510,,,,,,,,,
mondo:0018683,acquired ichthyosis,"['acquired ichthyosis', 'fish scale disease, acquired', 'ichthyosis acquisita', 'ichthyosis, acquired', 'acquired ichthyosis (disease)']",,,454,,,C112831,,C538175,,L85.0,,
mondo:0018684,idiopathic neonatal atrial flutter,['neonatal cardiac dysrhythmia'],,,45452,CN205105,,,,,,P29.1,,
mondo:0018685,incessant infant ventricular tachycardia,,,,45453,C0340487,,,,,,I47.2,,
mondo:0018686,acquired Creutzfeldt-Jakob disease,"['acquired Creutzfeldt Jacob disease', 'acquired CJD', 'sporadic CJD']",,,454700,CN237752,,,,C538481,,,,
mondo:0018687,progressive muscular atrophy,"['progressive spinal muscular atrophy', 'PMA', 'pure progressive muscular atrophy']",318,,454706,C0917981,,C85027,0008864,D009134,335.21,,,
mondo:0018688,anti-p200 pemphigoid,,,,454710,CN237754,,,0008597,,,,,
mondo:0018689,plasma cell leukemia,"['plasmacytic leukaemia', 'plasma cell leukemia', 'leukaemia plasmacytic', 'leukemia, plasma cell', 'leukemia plasmacytic', 'PCL', 'plasmacytic leukemia']",9513,,454714,C0023484,,C3180,0006475,D007952,203.10,,,
mondo:0018690,Holmes-Adie syndrome,"['Adie^s syndrome', 'poorly Reacting pupils', 'Adie pupil', 'tonic pupil-tendon areflexia syndrome', 'Adie^s pupil', 'Adie syndrome', 'Holmes-Adie syndrome', 'Adie^s pupil or syndrome', 'tonic, sluggishly reacting pupil and hypoactive or absent tendon reflexes', 'Adie^s pupil syndrome', 'tonic pupil']",11549,103100,454718,C0001519,"['-0.02509', '-0.1863', '0.09235', '-0.2214', '-0.0787', '-0.002928', '0.0623', '0.05988', '0.03973', '-0.1102', '0.12006', '0.222', '-0.5054', '-0.1611', '-0.2065', '0.04617', '-0.04633', '-0.252', '0.02597', '-0.691', '-0.1205', '0.1714', '0.0852', '0.07837', '0.0985', '0.1207', '-0.2634', '0.1871', '0.09406', '0.05576', '-0.02098', '0.06384', '0.207', '0.1599', '-0.03793', '0.01738', '0.3052', '0.1306', '-0.0592', '-0.2161', '0.02441', '-0.05368', '-0.00939', '-0.1993', '-0.0959', '0.0835', '-0.259', '0.1876', '0.3472', '0.583', '-0.04196', '0.02791', '-0.00598', '0.002668', '-0.3062', '0.1796', '0.605', '-0.314', '-0.341', '-0.001364', '0.07513', '0.2114', '0.044', '0.1663', '-0.2439', '0.02327', '0.3357', '0.666', '-0.1487', '0.2908', '-0.5103', '0.1945', '0.1467', '0.2695', '0.2075', '0.02063', '0.3596', '0.32', '0.0996', '-0.2155', '-0.09314', '0.0324', '0.2394', '0.3457', '0.1528', '-0.3037', '-0.161', '0.02567', '0.2642', '0.2152', '0.157', '0.4363', '0.4084', '-0.1493', '0.4673', '-0.007256', '0.2522', '-0.289', '-0.3228', '-0.0932']",C34357,0004126,D000270,,,,
mondo:0018692,variably protease-sensitive prionopathy,,,,454742,C4303527,,,,,,,,
mondo:0018694,isolated tracheo-esophageal fistula,"['isolated tracheoesophageal fistula', 'tracheoesophageal fistula', 'tracheo-esophageal fistula', 'H-type tracheoesophageal fistula']",,,454750,,,C35080,,,,,,
mondo:0018695,avian influenza,"['avian flu', 'bird flu']",4492,,454836,CN237762,,,0005222,D005585,,,,
mondo:0018696,corticobasal syndrome,,,,454887,CN237765,,,,,,,,
mondo:0018697,1p35.2 microdeletion syndrome,"['Del(1)(p35.2)', 'monosomy 1p35.2', 'deletion 1p35.2']",,,456298,CN237766,,,,,,,,
mondo:0018698,hereditary neuroendocrine tumor of small intestine,"['hereditary neuroendocrine tumor of small bowel', 'hereditary neuroendocrine tumour of the small intestine', 'hereditary neuroendocrine tumor of the small intestine', 'hereditary neuroendocrine tumour of small bowel', 'hereditary small intestine neuroendocrine neoplasm']",,,456333,CN847586,,,,,,,,
mondo:0018701,congenital nemaline myopathy,,,,457074,,,,,,,,,
mondo:0018702,Castleman-Kojima disease,"['TAFRO syndrome', 'thrombocytopenia-anasarca-fever-renal insufficiency-organomegaly syndrome']",,,457077,CN237773,,,,,,,,
mondo:0018703,isolated splenogonadal fusion,['SGF'],,,457083,CN242095,,,,,,,,
mondo:0018705,infantile-onset axonal motor and sensory neuropathy-optic atrophy-neurodegenerative syndrome,"['ANOAC', 'axonal neuropathy-optic atrophy-cognitive deficit syndrome']",,,457205,CN242083,,,,,,,,
mondo:0018706,syndromic sensorineural deafness due to combined oxidative phosphorylation defect,"['syndromic sensorineural hearing loss due to COXPD', 'syndromic sensorineural deafness due to COXPD']",,,457223,CN242144,,,,,,,,
mondo:0018708,squamous cell carcinoma of the oral tongue,"['OTSCC', 'oral tongue squamous cell carcinoma']",,,457252,CN242132,,,,,,,,
mondo:0018709,X-linked intellectual disability-hypotonia-movement disorder syndrome,,,,457260,,,,,,,,,
mondo:0018710,megalencephaly-severe kyphoscoliosis-overgrowth syndrome,,,,457359,,,,,,,,,
mondo:0018711,intellectual disability-muscle weakness-short stature-facial dysmorphism syndrome,,,,457365,CN242088,,,,,,,,
mondo:0018712,composite hemangioendothelioma,['composite hemangioendothelioma'],,,458758,CN242120,,C45475,,,,,,
mondo:0018713,retiform hemangioendothelioma,"['hobnail hemangioendothelioma', 'retiform hemangioendothelioma']",,,458763,CN242097,,C27511,,,,,,
mondo:0018714,primary intralymphatic angioendothelioma,"['papillary intralymphatic angioendothelioma', 'Dabska tumour', 'Dabska tumor', 'pila', 'malignant endothelial papillary angioendothelioma', 'papillary Endovascular angioendothelioma']",,,458768,CN242194,,C7526,,,,,,
mondo:0018715,congenital hemangioma,"['congenital hemangioma', 'congenital angioma']",,,458775,C0235753,,C3841,,,,,,
mondo:0018716,partially involuting congenital hemangioma,['PICH'],,,458785,,,C172209,,,,,,
mondo:0018717,mixed cystic lymphatic malformation,['mixed cystic lymphangioma'],,,458792,,,,,,,,,
mondo:0018720,common cystic lymphatic malformation,,,,458833,,,,,,,,,
mondo:0018724,X-linked intellectual disability-cerebellar hypoplasia-spondylo-epiphyseal dysplasia syndrome,,,,459070,CN242161,,,,,,,,
mondo:0018725,corpus callosum agenesis-macrocephaly-hypertelorism syndrome,"['dup(7)(q36.3)', '7q36.3 microduplication syndrome']",,,459074,CN242137,,,,,,,,
mondo:0018731,lethal multiple congenital anomalies/dysmorphic syndrome,,,,459787,,,,,,,,,
mondo:0018733,intellectual disability syndrome due to a DYRK1A point mutation,['DYRK1A-related intellectual disability syndrome due to a point mutation'],,,464311,CN242084,,,,,,,,
mondo:0018734,verrucous hemangioma,"['verrucous keratotic hemangioma', 'verrucous keratotic hemangioma (morphologic abnormality)']",470,,464318,CN242156,,C4299,,,,,,
mondo:0018735,multifocal lymphangioendotheliomatosis-thrombocytopenia syndrome,"['MALT1 wt allele', 'MLT', 'cutaneovisceral angiomatosis-thrombocytopenia syndrome', 'mucosa associated lymphoid tissue lymphoma translocation Gene 1 wt allele', 'DKFZp434L132', 'MLT1', 'multifocal lymphangioendotheliomatosis with thrombocytopenia']",,,464321,CN242151,,C60672,,,,,,
mondo:0018736,kaposiform lymphangiomatosis,['KLA'],,,464329,,,,,,,,,
mondo:0018737,catastrophic antiphospholipid syndrome,"['caps', 'catastrophic APS']",,,464343,CN242096,,,,,289.81,,,
mondo:0018738,benign metanephric tumor,,,,464359,CN242075,,,,,,,,
mondo:0018739,neonatal alloimmune neutropenia,,,,464370,C0272176,,,,,,P61.5,,
mondo:0018740,drug-induced methemoglobinemia,"['drug induced methemoglobinemia', 'acquired methemoglobinemia']",,,464453,C0271905,,C101045,,,,,,
mondo:0018741,paracetamol poisoning,['acetaminophen poisoning'],,,464458,,,,,,965.4,,,
mondo:0018742,familial gastric type 1 neuroendocrine tumor,"['familial type 1 gNET', 'hereditary type 1 gNET']",,,464756,CN242170,,,,,,,,
mondo:0018743,immune-mediated acquired neuromuscular junction disease,,,,464764,CN242076,,,,,,,,
mondo:0018744,oligodendroglial tumor,"['oligodendroglial tumor', 'oligodendroglial neoplasm']",,,46484,CN205116,,C6960,,,,,,
mondo:0018745,superficial pemphigus,,,,46485,CN227541,,,,,,,,
mondo:0018746,mucous membrane pemphigoid,"['mucosal pemphigoid', 'cicatricial pemphigoid with ocular involvement', 'benign mucosal pemphigoid', 'ocular pemphigus', 'Mucosynechial pemphigoid', 'benign mucous membrane pemphigoid', 'benign mucous Membrane pemphigoid', 'benign mucous membrance pemphigoid', 'ocular pemphigoid', 'benign mucous membrane pemphigoid with ocular involvement', 'cicatricial pemphigoid']",11656,,46486,,,C34907,1000680,,694.61,,10057052,
mondo:0018747,acquired epidermolysis bullosa,"['epidermolysis bullosa acquisita', 'EBA', 'EB acquisita', 'epidermolysis bullosa Aquisita', 'acquired epidermolysis bullosa']",4313,,46487,C0079293,,C84690,1000691,D016107,695.19,L12.3,10056508,
mondo:0018748,linear IgA Dermatosis,,,,46488,C0406650,,,,D062027,,,10024515,
mondo:0018749,hereditary persistence of fetal hemoglobin-beta-thalassemia syndrome,['HPFH-beta-thalassemia syndrome'],,613566,46532,CN205122,"['-0.5166', '0.3489', '-0.2032', '-0.843', '-0.2703', '-0.4707', '-0.7266', '1.351', '-1.147', '-1.066', '-0.2257', '0.0804', '0.261', '0.858', '-0.4668', '-0.2522', '-1.538', '-0.4524', '-0.504', '-0.9', '-0.4827', '-0.148', '1.062', '-0.208', '0.9214', '-0.01328', '0.723', '-0.3992', '0.4048', '-0.6333', '-0.278', '-0.27', '0.03995', '-0.4187', '-0.7524', '-0.2998', '-1.026', '-0.0419', '-0.4507', '-1.008', '0.2805', '0.1542', '0.379', '-0.2124', '-0.7207', '-0.758', '-0.5156', '-0.885', '0.3645', '-0.5605', '-0.1552', '-0.8174', '0.3499', '0.01385', '-0.011925', '0.1619', '-0.666', '0.705', '-0.01209', '0.4727', '-0.6323', '-0.02394', '0.10364', '-0.29', '-0.7334', '0.1321', '0.5796', '0.7783', '-1.276', '0.5513', '0.16', '0.414', '-0.2069', '-0.10486', '0.4675', '0.1914', '-0.2544', '0.1556', '-0.009735', '0.05692', '-0.1782', '-0.894', '0.11816', '-0.1339', '-0.3293', '0.02164', '0.4392', '0.3726', '-0.1171', '0.398', '0.3115', '0.1676', '-0.1489', '-0.1935', '0.608', '0.3386', '-0.419', '-0.3083', '-0.2247', '-0.6675']",,,,,,,
mondo:0018751,hereditary otorhinolaryngologic disease,['genetic otorhinolaryngologic disease'],,,466084,CN242186,,,,,,,,
mondo:0018752,exercise-induced malignant hyperthermia,['Exertional heat stroke'],,,466650,,,,,,,,,
mondo:0018754,cyanide poisoning,,,,466670,CN242145,,,,,989.0,,,
mondo:0018755,scorpion envenomation,,,,466677,CN242103,,,,,,,,
mondo:0018756,euthyroid Graves orbitopathy,['euthyroid Graves ophthalmopathy'],0081120,,466682,,,,,,,,,
mondo:0018757,supratip dysplasia,,,,466695,,,,,,,,,
mondo:0018758,familial patent arterial duct,,,,466729,CN242171,,,,,,,,
mondo:0018759,childhood-onset progressive contractures-limb-girdle weakness-muscle dystrophy syndrome,,,,466921,CN776870,,,,,,,,
mondo:0018760,DeSanto-Shinawi syndrome,['WAC-related facial dysmorphism-developmental delay-behavioral abnormalities syndrome'],0081126,,466943,CN242159,,,,,,,,
mondo:0018761,SMARCA4-deficient sarcoma of thorax,['SMARCA4-deficient thoracic sarcoma'],0080532,,466962,CN242100,,,,,,,,
mondo:0018762,non-acquired combined pituitary hormone deficiency,"['congenital hypopituitarism', 'congenital combined pituitary hormone deficiency']",,,467,,,,,,,E23.0,,
mondo:0018763,tubulinopathy-associated dysgyria,['brain stem asymmetry-superior cerebellar and basal ganglia dysplasia syndrome'],,,467166,CN242152,,,,,,,,
mondo:0018764,microcephalic primordial dwarfism due to RTTN deficiency,,,614833,468631,,,,,,,,,
mondo:0018765,cryptogenic multifocal ulcerous stenosing enteritis,['CMUSE'],,,468635,C4302263,,,,,,,,
mondo:0018766,chronic enteropathy associated with SLCO2A1 gene,['CEAS'],,,468641,,,,,,,,,
mondo:0018767,severe primary trimethylaminuria,"['fish odour syndrome', 'trimethylaminuria', 'fish malodor syndrome', 'fish odor syndrome', 'TMAU', 'TMAuria', 'stale fish syndrome', 'fish-odor syndrome']",0080361,602079,468726,,,,,C536561,,,,0003614
mondo:0018768,familial cold autoinflammatory syndrome,"['familial polymorphous cold eruption', 'FCAS', 'familial cold urticaria', 'FCU', 'familial cold autoinflammatory syndrome']",0090061,,47045,CN230757,"['0.2598', '0.09973', '-0.3787', '-0.012314', '0.03217', '-0.5044', '0.0605', '0.3943', '0.206', '-0.02106', '-0.02481', '0.915', '-0.4224', '-0.0699', '-0.3965', '0.2927', '0.5947', '-0.3713', '0.165', '-0.743', '0.1667', '-0.06445', '0.1744', '-0.516', '-0.05835', '0.4524', '-0.1942', '0.2399', '0.03412', '-0.0257', '-0.2294', '-0.1284', '0.0716', '0.4175', '0.0168', '-0.1798', '-0.4834', '-0.2478', '-0.1736', '0.5454', '-0.09717', '-0.693', '0.473', '-0.04025', '0.4395', '0.3647', '-0.1525', '0.4868', '0.895', '0.918', '-0.616', '0.0017605', '-0.3872', '-0.2825', '0.02756', '0.1836', '0.4949', '-0.632', '-0.281', '-0.4062', '0.1501', '0.305', '-0.4768', '-0.2025', '0.231', '0.01092', '0.4753', '0.6133', '0.0503', '0.4714', '-0.5176', '0.06195', '0.2491', '-0.574', '0.6167', '0.974', '0.128', '0.8574', '0.1674', '-0.273', '0.2673', '-0.505', '0.4744', '0.02603', '0.1678', '0.111', '0.01078', '0.7256', '0.128', '0.2454', '0.3306', '0.09753', '0.5986', '-0.1434', '0.653', '0.1573', '0.04578', '-0.5234', '-0.555', '-0.277']",C119053,,,,,10064570,
mondo:0018769,isosporiasis,"['Isosporosis', 'Cystoisospora belli caused disease or disorder', 'infection by Isospora belli and Isospora hominis', 'cystoisosporiasis']",2112,,472,C0311386,,C4076,0007232,D021865,,A07.3,10023076,
mondo:0018770,Jeune syndrome,"['asphyxiating thoracic dystrophy of the newborn', 'ATD', 'short-rib thoracic dysplasia with or without polydactyly', 'short-rib thoracic dysplasia', 'Jeune^s syndrome', 'Chondroectodermal dysplasia-like syndrome', 'infantile thoracic dystrophy', 'thoracic pelvic phalangeal dystrophy', 'asphyxiating thoracic dystrophy', 'Jeune asphyxiating thoracic dystrophy', 'Jeune syndrome', 'JATD']",0050592,,474,C0265275,"['-0.2769', '-0.3638', '0.3384', '-0.4333', '-0.08575', '-0.646', '0.11835', '0.4358', '-0.2311', '-0.7417', '-0.3652', '-0.3926', '0.0196', '-0.3074', '-0.02484', '-0.01974', '0.1602', '-0.1676', '-0.6143', '-1.093', '-0.004105', '0.293', '0.902', '0.2329', '-0.04135', '-0.0414', '-0.2081', '0.0487', '0.03796', '0.01686', '1.134', '-0.378', '0.1449', '-0.1152', '0.4692', '0.331', '0.285', '-0.272', '0.11584', '0.1952', '-0.08746', '0.3704', '0.642', '0.2761', '-0.606', '-0.12036', '-0.04324', '-0.2021', '0.1151', '-0.2625', '0.2051', '0.4531', '-0.08356', '-0.1277', '-0.1637', '-0.5625', '0.1947', '-0.2654', '-0.085', '-0.0506', '0.3335', '0.1685', '-0.07697', '0.3796', '-0.4277', '-0.4858', '0.637', '0.6104', '-0.3577', '0.5166', '-0.4204', '0.3438', '0.4026', '0.0984', '-0.113', '-0.5527', '0.1396', '0.02834', '-0.554', '-0.5146', '0.1793', '0.468', '-0.10016', '0.1897', '0.013695', '0.00529', '0.563', '0.03714', '-0.2262', '0.625', '-0.2402', '-0.673', '-0.8477', '0.08954', '0.567', '0.7485', '0.441', '-0.6245', '0.6895', '0.18']",C84794,,C537571,,,10057621,
mondo:0018771,congenital anomaly of ventricular septum,"['rare congenital anomaly of ventricular septum', 'congenital anomaly of interventricular communication', 'congenital heart malformation of interventricular septum', 'interventricular septum congenital heart malformation', 'congenital ventricular septal anomaly']",,,474347,,,,,,,,,
mondo:0018772,Joubert syndrome,"['CPD IV', 'Joubert-Boltshauser syndrome', 'JBTS', 'cerebellar vermis agenesis', 'classic Joubert syndrome', 'Joubert syndrome type A', 'pure Joubert syndrome', 'cerebelloparenchymal disorder IV']",0050777,,475,,"['0.2656', '0.2062', '-0.4631', '-0.3022', '-0.2482', '-0.2227', '0.1589', '1.122', '-0.961', '-0.2416', '-0.2372', '-0.6094', '0.1702', '-0.1338', '0.06223', '-0.3997', '0.6675', '-0.5493', '0.1517', '-0.576', '-0.067', '0.2615', '0.1133', '0.06384', '0.03302', '-0.221', '-0.1007', '-0.0238', '0.0741', '-0.04565', '0.4612', '-0.06964', '0.1658', '-0.1943', '-0.1069', '0.10754', '0.1246', '-0.153', '-0.2095', '-0.081', '-0.0845', '0.3145', '-0.4841', '0.3926', '-0.3184', '-0.1654', '0.1696', '0.4124', '0.0487', '0.2317', '-0.631', '0.6504', '-0.637', '-0.989', '-0.1871', '-0.4146', '0.0508', '0.1483', '-0.2612', '-0.1625', '0.04004', '0.405', '0.4475', '0.1985', '-0.1788', '-0.2803', '0.924', '0.1827', '0.134', '0.571', '-0.3826', '0.7583', '-0.01591', '0.3872', '0.09937', '-0.2147', '0.5527', '-0.3127', '-0.4185', '-0.007004', '0.3098', '-0.0303', '-0.4014', '0.2467', '0.0794', '0.1094', '0.01218', '0.1449', '-0.05804', '0.3733', '-0.2059', '0.1593', '-0.4216', '0.319', '0.4268', '0.013176', '0.2979', '-0.0656', '0.212', '0.1355']",C74996,,,,,,
mondo:0018773,autosomal dominant distal axonal motor neuropathy-myofibrillar myopathy syndrome,,,,476093,CN776822,,,,,,,,
mondo:0018774,erythrokeratodermia-cardiomyopathy syndrome,['EKC syndrome'],,,476096,CN776912,,,,,,,,
mondo:0018775,axonal hereditary motor and sensory neuropathy,['axonal HMSN'],,,476109,,,,,,,,,
mondo:0018776,demyelinating hereditary motor and sensory neuropathy,['demyelinating HMSN'],,,476116,,,,,,,,,
mondo:0018777,autosomal dominant preaxial polydactyly-upperback hypertrichosis syndrome,,,,476119,CN776826,,,,,,,,
mondo:0018778,intermediate Charcot-Marie-Tooth disease,"['Intermediate hereditary motor and sensory neuropathy', 'Charcot-Marie-Tooth disease dominant intermediate', 'Charcot-Marie-Tooth disease recessive intermediate', 'Charcot-Marie-Tooth disease intermediate type']",0050543,,476123,CN776860,,,,,,,,
mondo:0018779,hypercontractile muscle stiffness syndrome,,,,476403,CN776841,,,,,,,,
mondo:0018780,congenital generalized hypercontractile muscle stiffness syndrome,,,,476406,,,,,,,,,
mondo:0018781,KID syndrome,"['keratitis, ichthyosis, and deafness (KID) syndrome', 'keratitis-ichthyosis-deafness/Hystrix-like ichthyosis-deafness syndrome', 'Senter syndrome', 'KID/HID syndrome', 'ichthyosis hystrix Rheydt type']",,,477,CN205136,"['0.5283', '-0.4565', '-0.3997', '-0.503', '0.653', '-0.4717', '0.18', '0.3833', '-0.2974', '-0.649', '-0.1033', '-0.01304', '-0.473', '-0.2522', '-0.4421', '0.3767', '0.876', '-0.668', '-0.1622', '-0.4868', '-0.1475', '0.04388', '0.1921', '-0.3132', '-0.545', '-0.01619', '-0.7026', '0.268', '-0.6846', '-0.138', '0.285', '0.224', '0.06934', '0.5366', '0.166', '0.1552', '0.0876', '-0.5117', '-0.272', '0.1448', '0.1164', '-0.2585', '0.469', '-0.164', '-0.2693', '-0.254', '-0.5503', '0.011856', '-0.2233', '-0.4756', '-0.3457', '0.013115', '0.4258', '0.2317', '-0.4995', '-0.1054', '0.7495', '0.1265', '-0.5337', '-0.292', '-0.2284', '-0.002958', '-0.4844', '-0.07837', '-0.1159', '0.00904', '0.3926', '0.895', '0.1057', '1.135', '-0.0696', '-0.19', '-0.4807', '-0.05685', '0.8105', '-0.1721', '0.2776', '-0.385', '0.1412', '-0.01396', '-0.04013', '0.1312', '-0.0732', '0.8315', '-0.05276', '0.4314', '-0.2299', '0.524', '0.0642', '0.73', '0.7793', '0.4187', '0.1074', '0.636', '0.1359', '0.11346', '0.6064', '-0.557', '0.4346', '-0.01685']",,,C536168,759.89,,10048786,
mondo:0018782,type 1 interferonopathy,,,,477647,,,,,,,,,
mondo:0018783,fibroblastic rheumatism,,,,477650,C1302753,,,,,729.0,,,
mondo:0018784,pediatric multiple sclerosis,"['MS pediatric', 'multiple sclerosis, pediatric', 'pediatric MS', 'paediatric MS', 'multiple sclerosis, paediatric', 'MS paediatric']",,,477738,CN037005,,,,,,,,
mondo:0018786,pontine autosomal dominant microangiopathy with leukoencephalopathy,['PADMAL'],,,477749,,"['-0.01704', '0.02785', '0.0005856', '-0.01941', '0.0029', '-0.04187', '0.003056', '0.03925', '-0.03827', '-0.02725', '-0.01425', '-0.001473', '-0.00883', '-0.01214', '0.00047', '-0.01095', '-0.011566', '-0.02141', '-0.01231', '-0.05963', '-0.01299', '-0.0217', '0.02103', '-0.00535', '0.00227', '0.00215', '-0.01164', '-0.002502', '0.012794', '-0.0281', '0.02345', '0.004974', '0.03732', '0.02182', '0.010635', '-0.0194', '-0.006214', '-0.02425', '-0.003252', '-0.03534', '0.01591', '-0.02576', '0.02039', '0.001038', '-0.0094', '-0.03473', '-0.00975', '0.02158', '0.01094', '0.01303', '-0.004917', '0.002394', '-0.003782', '-0.006084', '-0.007664', '-0.00958', '0.0346', '-0.02165', '-0.03757', '0.001091', '0.02629', '0.02155', '0.00594', '-0.01067', '-0.00762', '0.01284', '0.04453', '0.04388', '-0.02025', '0.0383', '-0.02585', '0.001023', '0.001466', '-0.0299', '0.03156', '0.00922', '-0.0005784', '0.003378', '-0.02086', '-0.0191', '-0.005207', '0.00449', '0.001902', '0.03674', '0.001336', '0.01284', '0.01415', '0.0355', '0.02924', '0.01738', '0.011734', '0.02357', '-0.000272', '0.0002204', '0.0769', '0.03278', '0.03305', '-0.04065', '-0.002203', '0.01476']",,,,,,,
mondo:0018788,COL4A1 or COL4A2-related cerebral small vessel disease,['COL4A1 or COL4A2-related cerebral angiopathy'],,,477759,CN776854,,,,,,,,
mondo:0018791,Moyomoya angiopathy,,,,477768,,,,,,,,,
mondo:0018793,primary condylar hyperplasia,['type 1 condylar hyperplasia'],,,477781,,,,,,,,,
mondo:0018794,cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder,"['Phospholipase A2, Group Iva, Deficiency of', 'GURDP', 'GASTROINTESTINAL ULCERATION, RECURRENT, WITH DYSFUNCTIONAL PLATELETS', 'PLA2G4A-related platelet dysfunction', 'platelet dysfunction due to cytosolic phospholipase-A2 alpha deficiency']",,618372,477787,CN776897,,,,,,,,
mondo:0018795,syndromic constitutional thrombocytopenia,['syndromic constitutional thrombocytopenia'],,,477794,CN776900,,,,,,,,
mondo:0018796,isolated constitutional thrombocytopenia,"['non-syndromic constitutional thrombocytopenia', 'Cconstitutional thrombocytopenia without extra-hematopoietic manifestation']",,,477797,,,,,,,,,
mondo:0018800,Kallmann syndrome,"['Kallman syndrome', 'congenital hypogonadotropic hypogonadism with anosmia', 'Olfacto-genital pathological sequence', 'familial hypogonadism with anosmia', 'hypogonadism with anosmia', 'Kallman^s syndrome', 'hypogonadotropic hypogonadism with anosmia']",3614,,478,C0162809,"['-0.2283', '-0.1465', '0.2524', '-0.3057', '0.34', '0.112', '0.06015', '0.786', '-0.1598', '-0.1599', '-0.3037', '-0.2421', '-0.4014', '0.4104', '0.03384', '-0.1476', '0.1572', '0.0599', '-0.601', '-0.8306', '-0.7456', '-0.4465', '0.523', '-0.4314', '0.2742', '0.09076', '0.197', '-0.571', '0.1575', '-0.4326', '0.599', '-0.2607', '0.514', '0.2634', '-0.283', '-0.2184', '0.4001', '-0.3933', '-0.2257', '0.3818', '0.3564', '0.4448', '-0.2266', '-0.257', '0.372', '-0.3242', '0.11163', '-0.1948', '-0.2642', '0.6587', '-0.4236', '-0.5386', '-0.06396', '0.05444', '-0.7915', '0.8945', '0.341', '-1.111', '-0.6743', '0.5347', '0.03038', '0.309', '0.261', '-0.045', '-0.674', '0.3245', '0.3538', '0.04486', '-0.01189', '0.2087', '-0.1656', '0.1991', '0.1511', '-0.3577', '0.7427', '-0.772', '-0.1583', '-0.4084', '-0.4292', '-0.1796', '0.1942', '0.1064', '0.4927', '0.1366', '-0.5225', '-0.2339', '-0.09503', '-0.468', '0.2625', '-0.3586', '-0.2637', '0.6694', '-0.0676', '-0.05936', '0.2098', '-0.1787', '0.409', '-0.602', '0.0667', '0.4585']",C75479,,D017436,253.4,E23.0,10053142,
mondo:0018801,congenital bilateral absence of vas deferens,"['congenital bilateral agenesis of vas deferens', 'congenital bilateral aplasia of vas deferens']",0111862,,48,,"['-0.4646', '0.382', '0.03238', '-0.4365', '0.4048', '-0.106', '0.03918', '0.365', '-0.2408', '-0.07886', '0.3235', '-0.0742', '-0.2283', '-0.10645', '0.3672', '-0.5205', '0.12354', '0.445', '-0.1588', '-0.4597', '-0.4678', '-0.2998', '0.5396', '-0.4783', '0.383', '0.06604', '-0.01938', '0.0499', '0.3845', '-0.1237', '0.487', '-0.09686', '0.0805', '0.01602', '0.0936', '-0.5005', '-0.0668', '0.0875', '-0.02068', '-0.05872', '0.3774', '-0.05966', '0.0847', '0.01672', '-0.3472', '-0.4717', '0.1062', '0.11285', '0.1577', '0.2476', '-0.2395', '-0.0825', '-0.2015', '0.1758', '-0.3066', '0.011955', '0.74', '-0.0641', '-0.512', '0.3147', '0.7236', '0.5938', '0.5034', '0.1508', '0.2878', '-0.07574', '0.2434', '0.2098', '-0.518', '0.1399', '-0.4878', '-0.02916', '0.02101', '0.00893', '0.06335', '0.06635', '0.2642', '0.04703', '-0.5435', '0.2344', '0.0748', '0.2072', '0.4055', '-0.406', '-0.4895', '-0.6597', '0.277', '0.3672', '-0.0781', '-0.462', '-0.315', '0.096', '-0.387', '-0.402', '1.042', '-0.1553', '0.53', '-0.9023', '-0.2186', '-0.3777']",,,,752.89,,10010670,
mondo:0018804,MYO5B-related progressive familial intrahepatic cholestasis,['MYO5B deficiency'],,,480491,CN776887,,,,,,,,
mondo:0018805,bile duct cyst,"['choledochocele', 'choledochal cyst', 'congenital choledochal cyst', 'congenital cystic dilatation of the biliary tract', 'choledochal cysts', 'bile duct cysts']",899,603003,480501,,,,,D015529,751.69,Q44.4,,
mondo:0018806,primary intrahepatic lithiasis,"['PIHL', 'primary hepatolithiasis']",,,480506,,,,,,,,,
mondo:0018807,idiopathic ductopenia,"['IAD', 'idiopathic adult ductopenia']",,,480512,CN244899,,,,,,,,
mondo:0018808,Caroli syndrome,,,,480520,CN776859,,,,,,,,
mondo:0018809,idiopathic peliosis hepatis,['idiopathic peliosis hepatitis'],,,480524,,,,,,,,,
mondo:0018810,lethal hydranencephaly-diaphragmatic hernia syndrome,,,,480528,CN776878,,,,,,,,
mondo:0018811,congenital portosystemic shunt,['congenital portosystemic venous fistula'],,,480531,,,,,,,,,
mondo:0018812,MSH3-related attenuated familial adenomatous polyposis,"['MSH3-related attenuated FAP', 'MSH3-related AFAP', 'MSH3-related attenuated familial polyposis coli']",,,480536,CN776886,,,,,,,,
mondo:0018813,high grade B-cell lymphoma with MYC and/ or BCL2 and/or BCL6 rearrangement,,,,480541,,,,,,,,,
mondo:0018814,non-SCID combined immunodeficiency,"['non-SCID', 'non-severe combined immunodeficiency']",,,480549,,,,,,,,,
mondo:0018815,aneurysmal bone cyst,"['aneurysmal cyst of bone', 'aneurysmal bone cyst (disease)', 'aneurysmal cyst of the bone', 'aneurysmal bone cysts', 'aneurysmal bone cyst', 'ABC']",,606179,480553,,,C3516,,D017824,733.22,,,0012063
mondo:0018816,isolated neonatal sclerosing cholangitis,"['sclerosing cholangitis, neonatal', 'NSC']",,617394,480556,C4479344,,,,,,,,
mondo:0018818,facial diplegia with paresthesias,"['facial diplegia with paresthesias variant of Guillain-Barré syndrome', 'facial diplegia with paresthesias variant of GBS', 'facial diplegia with paresthesias variant of Guillain-BarrC) syndrome']",,,480701,CN776915,,,,,,,,
mondo:0018820,recurrent metabolic encephalomyopathic crises-rhabdomyolysis-cardiac arrhythmia-intellectual disability syndrome,"['metabolic encephalomyopathic crises, recurrent, with rhabdomyolysis, cardiac arrhythmias, and neurodegeneration', 'transport and golgi organization protein 2 (TANGO2) deficiency', 'MECRCN', 'transport and golgi organisation protein 2 (TANGO2) deficiency', 'TANGO2 deficiency']",,616878,480864,CN776869,,,,,,,,
mondo:0018821,X-linked female restricted facial dysmorphism-short stature-choanal atresia-intellectual disability,"['X-linked facial dysmorphism-short stature-choanal atrsia-intellectual disability syndrome limited to females', 'X-linked facial dysmorphism-short stature-choanal atresia-intellectual disability syndrome limited to females']",,,480880,CN776923,,,,,,,,
mondo:0018822,global developmental delay-visual anomalies-progressive cerebellar atrophy-truncal hypotonia syndrome,,,,480898,CN776946,,,,,,,,
mondo:0018823,X-linked intellectual disability-global development delay-facial dysmorphism-sacral caudal remnant syndrome,,,,480907,CN776924,,,,,,,,
mondo:0018824,pyoderma gangrenosum,,8553,,48104,C0085652,,,0006835,D017511,686.01,L88,10037635,
mondo:0018825,PYCR2-related microcephaly-progressive leukoencephalopathy,,,,481152,,,,,,,,,
mondo:0018826,Lewis-Sumner syndrome,"['multifocal acquired demyelinating sensory and motor neuropathy', 'MADSAM']",,,48162,C1695985,,,,,,,10065580,
mondo:0018827,familial chilblain lupus,"['hereditary chilblain lupus', 'hereditary Chilblain lupus']",,,481662,CN776917,,,,,,,,
mondo:0018828,pseudo-TORCH syndrome 2,"['pseudo-TORCH syndrome 2', 'PTORCH2', 'USP18 deficiency']",,617397,481665,C4479376,,,,,,,,
mondo:0018829,familial schizencephaly,"['familial schizencephaly', 'hereditary schizencephaly']",,,481986,CN776926,,,,C538514,,,,
mondo:0018830,Kimura disease,"['eosinophilic hyperplastic lymphogranuloma', 'angiolymphoid hyperplasia with eosinophilia', 'eosinophilic lymphofolliculosis', 'eosinophilic lymphofollicular granuloma', 'eosinophilic granuloma of soft tissue', 'Kimura^s disease', 'eosinophilic lymphogranuloma']",7365,,482,C0033838,,C26867,1000722,D000796,,,10048640,
mondo:0018831,HTRA1-related cerebral small vessel disease,['HTRA1-related cerebral angiopathy'],,,482072,CN776824,,,,,,,,
mondo:0018832,HTRA1-related autosomal dominant cerebral small vessel disease,['HTRA1-related autosomal dominant cerebral angiopathy'],,,482077,CN776823,,,,,,,,
mondo:0018835,nodular regenerative hyperplasia of the liver,"['nodular regenerative hyperplasia', 'non-cirrhotic nodular transformation', 'non-cirrhotic nodulation', 'non-cirrhotic portal hypertension', 'miliary hepatocellular adenomatosis']",,,48372,CN205145,,,,,573.8,,,
mondo:0018837,postinfectious vasculitis,,,,48435,C4510302,,,,,,,,
mondo:0018838,lissencephaly spectrum disorders,"['lissencephaly', 'lissencephaly (disease)', 'large gyri of cerebrum', 'Broad gyri of cerebrum', 'pachygyria', 'macrogyria']",0050453,,48471,C0266463,"['-0.2405', '0.1489', '0.223', '-0.2472', '0.2125', '-0.01303', '0.07355', '0.04123', '-0.3396', '-0.10004', '-0.379', '-0.10767', '0.001019', '-0.05307', '-0.2166', '-0.195', '0.1577', '-0.2869', '-0.2642', '-0.346', '0.1167', '0.05838', '0.4119', '-0.0374', '-0.0238', '-0.163', '-0.1696', '0.03488', '0.04428', '0.0824', '0.09265', '-0.02644', '0.2844', '0.1414', '0.1552', '0.2817', '0.03427', '0.0882', '-0.0446', '-0.5225', '0.2113', '-0.4043', '-0.1488', '-0.04584', '-0.00801', '-0.2852', '0.1351', '0.2737', '0.1597', '0.02168', '0.2452', '-0.10223', '-0.1401', '0.01099', '-0.3428', '-0.1401', '0.2131', '0.1175', '-0.3047', '0.05997', '0.06757', '0.10565', '0.07983', '0.1469', '-0.1081', '0.0517', '0.4907', '0.02829', '-0.437', '0.1992', '-0.2157', '0.3022', '0.1334', '0.133', '-0.2128', '0.098', '0.3616', '0.1605', '-0.3062', '-0.2048', '0.04086', '-0.03833', '-0.03186', '0.2185', '-0.1523', '-0.3872', '0.00786', '0.432', '0.003101', '-0.1171', '0.1875', '0.4011', '0.1665', '0.1681', '0.2411', '-0.177', '0.4514', '-0.2306', '0.1919', '0.29']",C103921,,D054082,,,10048911,0001339
mondo:0018839,acquired schizencephaly,['acquired schizencephaly'],,,485275,CN776925,,,,,,,,
mondo:0018840,isolated congenital hepatic fibrosis,"['nonsyndromic congenital hepatic fibrosis', 'congenital fibrose liver', 'congenital hepatic fibrosis', 'isolated CHF']",,,485426,C0009714,,C97071,,C562378,777.8,,,
mondo:0018841,congenital bile acid synthesis defect,"['bile acid synthesis defect, congenital', 'cholestasis with delta(4)-3-oxosteroid-5-beta-reductase deficiency', 'BASD', 'CBA']",0050674,,485631,CN239183,,,0009039,,,,,
mondo:0018842,primary effusion lymphoma,"['PEL', 'AIDS-related lymphoma', 'primary Effusion Lymphoma', 'body cavity-based lymphoma']",,,48686,C1292753,,C6915,1000491,D054685,202.80,,10065857,
mondo:0018843,embryonal carcinoma of the central nervous system,"['embryonal carcinoma of the CNS', 'embryonal carcinoma of CNS', 'central nervous system embryonal carcinoma', 'embryonal carcinoma', 'embryonal carcinoma of the central nervous system']",7232,,48736,C1333377,,C7010,,,,,,
mondo:0018844,urachal cyst,"['urachal cyst (disease)', 'urachal cyst']",,,488,,,C85216,,D014496,,,10065375,0012618
mondo:0018845,focal myositis,"['inflammatory pseudotumor of skeletal muscle', 'focal nodular myositis']",,,48918,,,,,,729.1,,,
mondo:0018846,penile agenesis,"['Aphallus', 'penis agenesis', 'micropenis', 'congenital absence of penis', 'agenesis of the penis', 'penis agenesia', 'Aphallia']",,,49,,,C99009,,C536649,,,,
mondo:0018847,omphalomesenteric cyst,,,,490,,,,,,,,,
mondo:0018848,IgG4-related retroperitoneal fibrosis,"['Ormond^s disease', 'Ormond disease', 'idiopathic retroperitoneal fibrosis', 'retroperitoneal fibrosis']",,,49041,,,C26876,,D012185,593.4,,10038979,
mondo:0018849,dentinogenesis imperfecta,"['DI', 'non-syndromic dentinogenesis imperfecta', 'DGI without OI', 'non-syndromic DGI', 'dentinogenesis imperfecta (disease)', 'opalescent teeth without osteogenesis imperfecta', 'dentinogenesis imperfecta without osteogenesis imperfecta', 'DGI', 'dentinogenesis imperfecta', 'opalescent teeth without OI']",4154,,49042,C0011436,,C84667,,D003811,520.5,,10054013,0000703
mondo:0018850,proliferating trichilemmal cyst,"['proliferating Pilar tumour', 'Pilar tumor', 'Pilar cyst', 'proliferating Pilar tumor', 'proliferating Tricholemmal tumor', 'proliferating pilar cyst', 'proliferating pilar cystic tumour', 'proliferating Tricholemmal tumour', 'proliferating trichilemmal tumour', 'proliferating trichilemmal tumor', 'proliferating pilar cystic tumor', 'Pilar tumour']",,,492,C2959585,,C27125,,,,,,
mondo:0018851,familial keratoacanthoma,"['multiple keratoacanthoma', 'hereditary keratoacanthoma']",,,493,CN227546,,,,,,,,
mondo:0018852,achromatopsia,"['Rod monochromatism', 'Rod monochromacy', 'total colour blindness', 'complete or incomplete color blindness', 'monochromatism', 'total color blindness', 'complete or incomplete colour blindness', 'ACHM', 'Pingelapese blindness']",13911,,49382,C0152200,,C84528,,,368.54,H53.51,10000454,
mondo:0018853,transgrediens et progrediens palmoplantar keratoderma,"['keratosis palmoplantaris transgrediens et progrediens', 'Greither disease', 'transgrediens et progrediens PPK', 'progressive diffuse PPK', 'progressive diffuse palmoplantar keratoderma', 'keratosis extremitatum hereditaria progrediens']",,,495,CN205162,,,,,,,,
mondo:0018854,acquired purpura fulminans,"['acquired PF', 'acquired purpura fulminans']",,,49566,CN205163,,,,D055665,,,10037556,
mondo:0018855,keratosis pilaris atrophicans,"['amelogenesis imperfecta, hypoplastic-hypomaturation, X-linked 2', 'Atrophodermia reticulata symmetrica faciei', 'folliculitis ulerythematosa', 'Atrophodermia vermiculata', 'folliculitis ulerythematosa reticulata', 'ulerythema ophryogenes', 'ulerythema ophryogenes with multiple congenital anomalies', 'honeycomb atrophy', 'keratosis pilaris atrophicans', 'Atrophodermia reticulata', 'burnett Schwartz Berberian syndrome', 'keratosis pilaris', 'keratosis pilaris atrophicans facies', 'ulerythema ophryogenesis', 'KPA']",0080751,604093,498,,"['0.55', '0.563', '0.0492', '-0.06885', '-0.1136', '-0.471', '0.0927', '0.2095', '-0.5576', '-0.05234', '0.4873', '0.6733', '-0.4941', '0.06226', '-0.353', '0.10443', '-0.2764', '-0.2379', '-0.4368', '-0.3826', '-0.2292', '-0.1511', '0.2554', '0.05444', '-0.01761', '0.09235', '-0.4102', '0.4263', '0.03415', '-0.3984', '0.02715', '-0.2556', '-0.234', '-0.3872', '0.074', '0.7007', '-0.3196', '-0.005867', '0.1205', '-0.674', '0.274', '0.05682', '-0.3652', '-0.00379', '0.11957', '-0.2642', '0.128', '0.3992', '0.3694', '0.01974', '-0.1646', '0.05173', '0.2737', '-0.2185', '-0.134', '-0.2393', '0.1007', '0.3281', '-0.6997', '-0.4634', '-0.0722', '0.146', '-0.2213', '0.2986', '0.28', '0.1918', '0.655', '0.5845', '0.2222', '0.9087', '-0.3625', '0.009895', '0.4146', '-0.0753', '-0.348', '-0.04645', '-0.1276', '0.4263', '0.2715', '-0.3447', '0.516', '-0.7476', '-0.3284', '-0.1021', '-0.006454', '-0.603', '-0.269', '0.3125', '0.4526', '0.789', '0.4119', '0.171', '-0.1261', '0.06134', '0.511', '-0.4128', '-0.2051', '-0.5356', '-0.11115', '0.2163']",,,C537412,757.39,,,
mondo:0018856,lichen amyloidosis,"['amyloid lichen', 'lichen amyloidosus']",,,49804,,,,,,,,,
mondo:0018857,creeping myiasis,['migratory myiasis'],,,504,C1562462,,,,D007815,,,10059547,
mondo:0018858,Graham Little-Piccardi-Lassueur syndrome,"['Graham Little syndrome', 'Piccardi-Lassueur-Little syndrome', 'Graham-Little-Piccardi-Lassueur syndrome']",,,505,CN205176,,,,,,L66.1,,
mondo:0018860,microlissencephaly-micromelia syndrome,['Basel-Vanagaite-Sirota syndrome'],,,50810,CN205181,,,,,,,,
mondo:0018861,Zellweger-like syndrome without peroxisomal anomalies,['AHN-Lerman-Sagie syndrome'],,,50812,CN205183,,,,,,,,
mondo:0018864,Kikuchi-Fujimoto disease,"['Kikuchi-Fujimoto^s disease', 'nosocomial Kikuchi^s disease', 'histiocytic necrotising lymphadenitis', 'Kikuchi^s disease', 'Kikuchi necrotizing lymphadenitis', 'Kikuchi disease', 'histiocytic necrotizing lymphadenitis']",,,50918,C0398367,,C71719,,D020042,,,,
mondo:0018865,striate palmoplantar keratoderma,"['keratosis palmoplantaris varians of Wachters', 'keratosis palmoplantaris striata', 'keratosis palmoplantaris striata et areata']",0081105,,50942,CN205191,"['0.3452', '0.3552', '-0.09973', '-0.317', '0.0451', '-0.383', '-0.3633', '0.03076', '-0.02211', '0.1656', '-0.3916', '0.2067', '-0.4604', '0.05612', '-0.1881', '0.1666', '0.3594', '-1.003', '-0.02806', '-1.2', '-0.287', '-0.1494', '0.739', '0.3372', '0.2979', '0.3118', '-0.1783', '0.4646', '0.01408', '0.1339', '0.1353', '-0.6006', '-0.1884', '0.0476', '0.3076', '-0.0363', '-0.269', '-0.03552', '0.0703', '-0.4026', '0.0929', '-0.6553', '0.0889', '-0.01569', '0.313', '-0.2151', '-0.3188', '0.298', '-0.09045', '0.0903', '0.06464', '0.1849', '0.2233', '0.305', '-0.4258', '-0.03717', '0.825', '0.2866', '-0.5356', '-0.3484', '0.09393', '0.0566', '-0.495', '-0.03342', '-0.05157', '0.1248', '0.5996', '0.493', '0.3408', '0.6694', '-0.3806', '0.04346', '0.6113', '-0.1323', '0.2358', '-0.0948', '0.2375', '-0.167', '0.1189', '-0.6987', '-0.3079', '0.2045', '0.3528', '-0.0785', '0.1821', '-0.4453', '-0.7847', '0.8076', '0.2664', '0.1691', '0.1628', '-0.02585', '0.0559', '0.4028', '0.369', '0.2047', '0.2708', '-0.1656', '0.1401', '0.1472']",,,,,,,
mondo:0018866,Aicardi-Goutieres syndrome,"['pseudotoxoplasmosis syndrome', 'Cree encephalitis', 'encephalopathy with basal ganglia calcification', 'encephalopathy, familial infantile, with calcification of basal ganglia and chronic cerebrospinal fluid lymphocytosis', 'encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid', 'Aicardi-Goutières syndrome', 'Aicardi Goutieres syndrome', 'AGS']",0050629,,51,,"['-0.292', '0.445', '-0.2097', '-0.239', '-0.2461', '-0.6416', '-0.4495', '1.069', '-0.951', '-0.0655', '-0.7456', '-0.2466', '0.1243', '-0.625', '0.09424', '-0.0655', '0.684', '0.1449', '-0.2015', '-0.4614', '-0.0613', '-0.1605', '0.3123', '-0.1658', '0.3096', '-0.257', '0.1558', '0.4565', '-0.2281', '0.1448', '-0.11426', '-0.04037', '0.409', '-0.29', '-0.3025', '0.701', '-0.324', '-0.1224', '-0.04898', '0.2786', '0.3975', '-0.518', '0.2568', '-0.3362', '0.02017', '-0.0803', '-0.1991', '-0.4653', '0.0633', '-0.158', '0.1499', '0.4495', '-0.898', '-0.2644', '0.2145', '0.3296', '0.2664', '-0.1824', '-0.293', '0.0947', '0.6777', '0.1443', '0.1206', '0.0788', '0.12396', '0.05737', '0.2155', '0.4956', '-0.5317', '0.217', '-0.02258', '0.8823', '-0.0369', '-0.11804', '0.003542', '0.1705', '0.5967', '0.3853', '-0.2773', '-0.3706', '-0.2668', '-0.2124', '-0.525', '0.1416', '0.07916', '0.5273', '0.3535', '0.549', '-0.4014', '0.264', '0.561', '0.531', '0.1494', '-0.09094', '0.4285', '0.4453', '0.5327', '-0.5615', '0.3013', '-0.06226']",,,C535607,333.0,,,
mondo:0018868,metachromatic leukodystrophy,"['deficiency of cerebroside-sulfatase', 'MLD', 'Scholz cerebral sclerosis', 'sulfatide lipoidosis', 'arylsulfatase A deficiency']",10581,,512,C0023522,"['0.0396', '0.6787', '0.4585', '0.4277', '-0.11334', '-0.457', '-0.59', '0.589', '-0.637', '0.1333', '-0.05814', '0.0748', '-0.131', '0.1656', '0.3176', '-0.1595', '-0.4712', '-0.122', '-0.623', '-0.03983', '-0.3076', '-0.5444', '-0.2815', '0.05115', '0.4194', '-0.736', '-0.7627', '0.0739', '-0.3506', '0.01021', '0.06055', '0.2605', '0.451', '-0.0384', '0.1254', '-0.152', '-0.901', '-0.1467', '0.3997', '-0.1583', '0.69', '-0.585', '0.1334', '0.5938', '0.2522', '-0.3716', '0.3213', '-0.9097', '0.2169', '0.887', '0.4966', '0.2335', '-0.3171', '-0.4062', '0.3032', '-0.5923', '0.2311', '0.4946', '-0.1649', '-0.3455', '-0.05975', '0.2316', '0.92', '0.284', '-0.3193', '0.2', '0.2048', '0.2473', '-0.6665', '-0.52', '-0.2151', '0.03091', '0.09735', '-0.57', '0.2184', '0.3328', '0.1236', '1.024', '-0.1805', '-0.1329', '0.099', '-0.5366', '-0.5137', '0.1078', '0.5215', '0.2422', '0.9688', '0.1372', '0.557', '0.6562', '0.02306', '0.736', '-0.3408', '0.4727', '0.585', '0.01743', '-0.2678', '-0.559', '0.3823', '0.2365']",C61251,,D007966,,,10067609,
mondo:0018869,cobblestone lissencephaly,['lissencephaly type 2'],,,51577,,,,,D054222,,,,
mondo:0018870,arterial calcification of infancy,"['occlusive infantile arteriopathy', 'generalised arterial calcification in infancy', 'idiopathic infantile arterial calcification', 'generalized arterial calcification in infancy', 'generalized arterial calcification of infancy', 'infantile arteriosclerosis', 'IIAC', 'generalised arterial calcification of infancy', 'idiopathic obliterative arteriopathy']",0050644,,51608,,"['-0.1932', '0.1498', '-0.377', '-0.02156', '0.3374', '-0.5273', '0.0886', '0.9526', '-0.4006', '0.485', '-0.5635', '-0.01862', '0.322', '0.07117', '-0.2715', '-0.2261', '-0.004917', '0.1827', '0.2135', '-0.5273', '0.3618', '-0.3535', '0.8286', '-0.343', '0.1076', '0.3115', '0.4849', '0.4395', '-0.04', '-0.2065', '0.2903', '-0.0902', '0.04297', '-0.481', '-0.12146', '-0.09076', '-0.1078', '-0.1803', '0.4924', '-0.1117', '0.276', '-0.3467', '0.994', '0.11414', '0.3313', '0.1399', '-0.2471', '-0.09973', '-0.6436', '0.362', '-0.1917', '-0.00679', '0.676', '0.03207', '-0.3113', '-0.3733', '-0.04968', '0.2988', '-0.03458', '0.09326', '0.3962', '0.522', '-0.2202', '-0.3232', '0.5806', '-0.04495', '0.4468', '0.5347', '-0.5874', '0.3804', '-0.2168', '-0.10065', '0.279', '-0.2289', '-0.548', '-0.03894', '0.272', '-0.2124', '-0.2832', '-0.01071', '-0.1218', '0.1592', '-0.2096', '0.4402', '-0.1461', '0.3416', '0.08246', '0.04642', '0.1798', '-0.1852', '0.5015', '0.1321', '-0.2537', '0.4172', '0.1119', '0.0831', '0.876', '0.1692', '-0.10846', '-0.7393']",,,C537440,,,,
mondo:0018871,acute myelomonocytic leukemia M4,"['acute myelomonocytic leukaemia (FAB type M4)', 'AML-M4', 'acute myeloblastic leukemia type 4', 'AML M4', 'acute myelomonocytic leukaemia', 'acute myeloblastic leukaemia type 4', 'acute myelomonocytic leukemia', 'AMMoL', 'acute myelomonocytic leukemia (FAB type M4)', 'acute M4 myeloid leukaemia', 'acute M4 myeloid leukemia', 'AMML']",0081082,,517,C0023479,,C7463,0000223,,,,10000890,
mondo:0018872,acute megakaryoblastic leukemia,"['acute myeloid leukemia M7', 'acute myeloblastic leukemia type 7', 'leukemia, megakaryocytic, malignant', 'AML M7', 'acute M7 myeloid leukaemia', 'acute myeloblastic leukaemia type 7', 'acute megakaryoblastic leukemia', 'megakaryocytic leukemia', 'acute megakaryoblastic leukemia (FAB type M7)', 'acute megakaryocytic leukaemia', 'acute M7 myeloid leukemia', 'thrombocytic leukemia', 'acute megakaryoblastic leukaemia (FAB type M7)', 'megakaryocytic myelosis', 'acute megakaryocytic leukemias', 'FAB M7', 'acute megakaryocytic leukemia', 'acute myeloid leukaemia M7', 'AMKL', 'acute megakaryoblastic leukemia, FAB M7', 'thrombocytic leukaemia', 'megakaryocytic leukaemia']",8761,,518,C0023462,,C3170,0003025,D007947,207.2,,C0023462,
mondo:0018873,anterior cutaneous nerve entrapment syndrome,"['intercostal nerve syndrome', 'rectus abdominis syndrome', 'ACNES']",,,51890,CN776944,,,,,,,,
mondo:0018874,acute myeloid leukemia,"['leukemia, myelocytic, acute', 'acute myeloblastic leukaemia', 'myeloid leukemia, acute, M4/M4Eo subtype, somatic', 'acute myelocytic leukemia', 'acute myeloid leukemia, somatic', 'acute non lymphoblastic leukaemia', 'acute myeloid leukemia (AML)', 'hematopoeitic - acute Myleogenous leukaemia (AML)', 'leukemia, acute myeloid, reduced survival in, somatic', 'leukemia, acute myeloid, susceptibility to, autosomal dominant, somatic mutation', 'acute non lymphoblastic leukemia', 'acute myelogenous leukemia', 'hematopoeitic - acute Myleogenous leukemia (AML)', 'AML', 'ANLL', 'acute myelogenous leukaemia', 'acute myelocytic leukaemia', 'leukemia, acute myeloid, somatic', 'acute myelogenous leukemias', 'acute myeloid leukaemia (AML)', 'leukemia, acute myelogenous', 'leukemia, acute myeloid, susceptibility to', 'acute Nonlymphocytic leukemia', 'AML - acute myeloid leukemia', 'leukemia, acute myeloid', 'myeloid leukemia, acute', 'acute Nonlymphocytic leukaemia', 'AML - acute myeloid leukaemia', 'acute myeloid leukemia', 'leukemia, acute myeloid, autosomal dominant, somatic mutation', 'acute myeloblastic leukemia', 'acute granulocytic leukaemia', 'acute nonlymphocytic leukemia', 'acute granulocytic leukemia', 'acute nonlymphocytic leukaemia']",9119,601626,519,C0023467,"['0.3472', '-0.0826', '-0.3628', '0.09393', '-0.0312', '0.01889', '0.6045', '1.284', '0.04706', '-0.4404', '0.3306', '0.179', '-0.298', '0.1824', '-0.228', '0.1492', '-0.2908', '-0.4526', '0.09314', '0.0643', '-0.2104', '-0.3452', '0.655', '-0.3982', '0.10284', '-0.4148', '0.297', '-0.2366', '-0.4788', '0.09863', '0.853', '0.4045', '0.8237', '0.2423', '0.1823', '0.2854', '-0.8564', '0.0864', '-0.5312', '-0.6016', '0.1569', '0.01575', '-0.08136', '-0.0141', '0.02222', '-0.0953', '-0.4124', '-0.594', '0.5723', '0.217', '0.8145', '-0.131', '0.3625', '0.1405', '0.2028', '-0.07086', '-0.645', '0.1693', '-0.595', '-0.185', '-0.2247', '0.431', '-0.1453', '-0.1621', '-0.4001', '0.124', '0.2178', '0.09595', '-0.00964', '1.269', '-0.04327', '0.03125', '-0.007412', '-0.5176', '0.3274', '0.4763', '0.03873', '0.2593', '0.2307', '-0.05325', '-0.3643', '-0.3723', '-0.05676', '-0.2284', '-0.7847', '-0.4854', '0.7197', '0.6665', '0.674', '-0.258', '0.259', '-0.06256', '-1.313', '-0.429', '0.4644', '0.946', '-0.3674', '-0.2042', '-0.2668', '-0.3418']",C3171,0000222,D015470,205.00,,10000880,
mondo:0018875,Li-Fraumeni syndrome,"['Li-Fraumeni syndrome', 'SBLA syndrome (sarcoma, breast, leukemia, and adrenal gland)', 'sarcoma family syndrome of Li and Fraumeni', 'sarcoma family syndrome of 51 and Fraumeni', 'sarcoma, breast, leukaemia and adrenal gland syndrome', 'TP53 Li-Fraumeni syndrome', 'LFS1', 'Li Fraumeni syndrome', 'SBLA syndrome', 'Li-Fraumeni-like syndrome', 'Li-Fraumeni familial cancer susceptibility syndrome', 'sarcoma, breast, leukemia and adrenal gland syndrome', 'Li-Fraumeni familiar cancer susceptibility syndrome', 'LFS3', 'Li-Fraumeni syndrome caused by mutation in TP53', 'LFS']",3012,609266,524,C0085390,"['0.709', '0.3823', '-0.1661', '0.3745', '0.5205', '-0.3967', '0.3032', '0.6094', '-0.11414', '-0.4111', '0.4185', '0.6846', '0.4597', '0.1248', '0.1786', '-0.691', '0.3262', '-0.09796', '-0.488', '-0.148', '-0.4473', '-0.6035', '0.2822', '-0.596', '0.214', '-0.011055', '0.1721', '0.2344', '0.3125', '-0.4443', '0.9194', '-0.308', '0.5356', '-0.2786', '0.2903', '0.2883', '-0.6797', '-0.412', '0.0757', '-0.506', '0.1714', '-0.7437', '0.1461', '-0.652', '0.809', '-0.10815', '-0.321', '0.1586', '0.2852', '-0.503', '0.594', '0.1698', '-0.6484', '-0.0643', '-0.3884', '0.02199', '0.3513', '0.425', '-0.3972', '0.04572', '0.713', '0.2035', '-0.33', '-0.05545', '-0.6143', '0.674', '0.764', '-0.02275', '-0.09174', '0.2722', '0.368', '-0.3828', '-0.3872', '-0.04565', '0.3857', '-0.6943', '-0.3938', '-0.0242', '-0.1736', '-0.514', '-0.439', '0.676', '0.8945', '0.7114', '-1.022', '0.1772', '0.4717', '0.2903', '0.5386', '-0.1853', '0.4666', '0.1177', '-0.4976', '-0.2935', '0.5576', '0.03099', '0.656', '-0.267', '-0.2622', '-0.2793']",C3476,,D016864,V84.01,,10066795,
mondo:0018876,mantle cell lymphoma,"['classical mantle cell lymphoma', 'LCM', 'mantle cell lymphoma', 'mantle zone lymphoma', 'MCL', 'lymphoma, mantle cell']",0050746,,52416,,,C4337,1001469,D020522,200.40,,10061275,
mondo:0018877,retinitis punctata albescens,,,,52427,CN205224,"['-0.337', '0.08276', '-0.10834', '-0.08044', '0.0373', '-0.3506', '-0.298', '0.3252', '-0.2668', '-0.2386', '-0.2566', '-0.11615', '-0.3027', '0.1035', '-0.0459', '-0.5015', '0.0822', '-0.1816', '0.0423', '-0.4717', '-0.175', '-0.1833', '0.02995', '0.2484', '0.0314', '0.453', '-0.2285', '-0.09424', '-0.312', '0.2389', '0.3223', '-0.11633', '-0.06647', '0.1586', '0.1006', '0.3005', '-0.002192', '-0.1663', '-0.08215', '-0.2094', '0.098', '-0.328', '0.2634', '0.0696', '-0.22', '0.1688', '-0.1743', '-0.05908', '0.01389', '0.1046', '0.353', '0.2286', '0.01953', '-0.3115', '0.0992', '-0.2426', '0.5933', '-0.183', '-0.2499', '-0.03177', '0.18', '-0.1241', '0.1941', '0.216', '-0.1125', '0.1066', '0.4392', '0.553', '-0.1236', '0.4976', '-0.1904', '-0.11255', '0.2014', '-0.1554', '0.4966', '-0.1279', '-0.05362', '0.03452', '-0.09314', '-0.2262', '0.07733', '-0.2246', '0.1346', '0.6777', '-0.06757', '-0.1387', '-0.0719', '0.0673', '0.2852', '0.046', '0.11664', '0.2025', '0.291', '0.368', '0.2998', '-0.1181', '0.2834', '-0.4062', '0.1145', '0.1118']",,,,,H35.5,,
mondo:0018878,branchiootic syndrome,"['bor', 'branchiootic dysplasia', 'bo syndrome']",0060232,,52429,CN205225,"['0.07385', '0.0976', '0.4922', '-0.379', '0.09814', '-0.01997', '0.511', '0.7344', '-0.3347', '-0.2223', '-0.3682', '-0.6675', '-0.3318', '-0.1309', '-0.552', '-0.4429', '0.01331', '-0.1848', '-0.199', '-0.08405', '0.0225', '-0.05518', '0.2952', '-0.0555', '0.6313', '0.3518', '-0.7324', '0.04803', '0.34', '-0.1333', '0.2048', '-0.2021', '0.10205', '0.263', '0.2961', '-0.2462', '0.06046', '-0.327', '-0.3977', '-0.728', '-0.2448', '0.2227', '0.4568', '-0.3652', '0.4963', '-0.6484', '-0.2815', '0.332', '0.03232', '0.2754', '-0.1654', '-0.004772', '0.1139', '-0.1603', '-0.63', '-0.2954', '0.2067', '-0.05154', '-0.4321', '-0.1849', '0.2544', '0.2468', '-0.365', '0.2732', '-0.2069', '-0.1841', '0.281', '0.3196', '-0.2156', '0.3567', '-0.2769', '0.04694', '0.363', '-0.308', '-0.0723', '-0.3262', '0.4019', '-0.0888', '-0.3792', '-0.2461', '0.03586', '-0.128', '0.199', '0.5425', '-0.52', '-0.3118', '0.1891', '1.074', '-0.08594', '0.1555', '-0.01698', '0.704', '0.2012', '0.2644', '0.554', '-0.3533', '0.739', '-0.6514', '0.1594', '0.5347']",,,C537104,,,,
mondo:0018879,lichen planopilaris,"['lichen follicularis', 'lichen planus follicularis', 'Kossard disease', 'LPP', 'frontal fibrosing alopecia (subtype)', 'follicular lichen planus', 'lichen planopilaris classic type']",,,525,C0023645,,,,C535892,,L66.1,,
mondo:0018881,myelodysplastic syndrome,"['smoldering leukemia', 'MDS, unclassifiable', 'hematopoeitic - myelodysplastic syndrome (MDS)', 'MDS-U', 'preleukemia', 'myelodysplastic syndrome, somatic', 'myelodysplastic neoplasm', 'dysmyelopoietic syndrome', 'myelodysplastic syndrome', 'myelodysplastic syndromes', 'oligoblastic leukemia', 'myelodysplastic syndrome/neoplasm', 'oligoblastic leukaemia', 'myelodysplastic syndrome, unclassifiable', 'MDS', 'smouldering leukaemia', 'myelodysplasia', 'myelodysplastic syndrome, susceptibility to']",0050908,614286,52688,C3463824,"['0.0314', '0.1259', '-0.277', '-0.03915', '0.0432', '0.0948', '0.3054', '0.1827', '0.0688', '-0.25', '0.2089', '-0.1144', '-0.015366', '0.118', '-0.1219', '-0.158', '-0.1718', '-0.3486', '0.1144', '-0.3225', '-0.05762', '-0.2299', '0.4846', '-0.3936', '0.1271', '-0.012985', '-0.0417', '-0.1874', '-0.1445', '-0.06335', '0.1483', '-0.04767', '0.2974', '0.0708', '0.0816', '0.08844', '-0.086', '-0.249', '0.034', '-0.2212', '0.04037', '-0.0596', '0.0793', '-0.3806', '0.006107', '-0.0992', '-0.4307', '-0.06012', '0.1829', '-0.1589', '0.1656', '-0.0776', '0.1422', '0.2832', '-0.0945', '0.01988', '0.387', '-0.1841', '-0.4578', '0.09937', '0.2032', '0.157', '0.006023', '-0.1589', '0.0838', '0.0833', '0.06305', '0.03976', '0.0526', '0.574', '-0.08746', '-0.1069', '-0.09344', '-0.0815', '0.1418', '0.2766', '-0.10736', '-0.1694', '0.01862', '-0.2272', '-0.1678', '-0.001536', '-0.07654', '0.05896', '-0.2874', '-0.08057', '0.3845', '0.4722', '0.1891', '0.0837', '0.1472', '-0.2869', '-0.3132', '-0.2441', '0.4492', '0.0723', '0.368', '-0.4197', '-0.2438', '-0.11334']",C3247,0000198,,238.75,,10028532,
mondo:0018882,vasculitis,"['systemic vasculitis', 'angiitis']",865,,52759,C0042384,"['0.1968', '0.2065', '-0.4395', '0.3674', '0.4714', '0.0706', '0.3145', '-0.2384', '-0.3748', '-0.2852', '0.3235', '-0.06757', '-0.04138', '0.8433', '-0.4426', '-0.4238', '-0.514', '0.1584', '0.2944', '0.01706', '-0.3044', '-0.1633', '0.3599', '0.0953', '0.0656', '0.1307', '-0.706', '0.701', '0.3809', '-0.3164', '0.979', '-0.1545', '0.8276', '0.144', '0.1183', '0.3066', '-0.874', '-0.01362', '-0.3416', '-0.5513', '0.2076', '0.05365', '0.0829', '-0.9653', '0.4077', '0.2922', '-0.338', '0.01894', '0.1749', '0.431', '0.5835', '0.1512', '0.685', '-0.2152', '0.04227', '-0.10345', '-0.2637', '-0.01982', '-0.7637', '-0.7324', '-0.889', '0.1996', '-0.4924', '0.0797', '-0.2211', '0.5186', '-0.2239', '0.7534', '-0.2983', '0.8403', '-0.0798', '-0.3083', '0.0277', '-0.428', '0.916', '0.719', '0.2208', '0.727', '0.1906', '-0.527', '-0.486', '-0.5093', '-0.1425', '-0.03738', '0.2214', '-0.3562', '0.3884', '-0.2045', '0.4985', '0.1209', '0.6216', '0.0884', '0.501', '-0.03177', '0.4067', '0.662', '-0.09546', '0.03156', '-0.3525', '-0.2012']",C26912,0006803,D014657,,,10047115,
mondo:0018883,Berardinelli-Seip congenital lipodystrophy,"['generalized congenital lipodystrophy', 'congenital generalised lipodystrophy', 'Lawrence-Seip syndrome', 'Berardinelli lipodystrophy syndrome', 'BSCL', 'Seip-Bernardinelli syndrome', 'lipoatrophic diabetes', 'Berardinelli Seip syndrome', 'congenital generalized lipodystrophy', 'GCL', 'Brunzell syndrome', 'generalised congenital lipodystrophy', 'total lipodystrophy', 'Beradinelli-Seip syndrome']",,,528,,"['0.5312', '-0.2197', '-0.44', '-0.3323', '0.2119', '-0.4702', '0.579', '0.6455', '0.0638', '-0.263', '-0.5664', '0.0808', '0.4758', '0.2441', '-0.5107', '-0.04538', '-0.0551', '0.292', '-0.313', '-0.8057', '-0.1108', '-0.551', '0.7065', '0.05542', '-0.1516', '0.423', '-0.073', '-0.4072', '0.145', '-0.766', '1.486', '-0.0203', '0.8267', '0.261', '-0.5405', '0.02715', '-0.209', '0.1954', '-0.3984', '-0.3728', '-0.2556', '-0.178', '0.149', '0.6426', '-0.05887', '-0.0627', '-0.01438', '0.255', '-0.3027', '0.3555', '0.0604', '0.0665', '1.081', '0.1422', '-0.1265', '-0.1743', '0.11786', '0.02312', '-0.3826', '0.02736', '-0.1359', '0.166', '0.2336', '-0.3394', '-0.5303', '0.1234', '-0.2642', '0.03268', '-0.2861', '-0.1388', '-0.1422', '0.2744', '0.126', '0.1537', '0.267', '-0.2773', '0.0879', '-0.6284', '-0.3538', '0.0687', '0.12177', '0.3508', '-0.2559', '0.3035', '-0.2673', '0.409', '-0.04385', '0.02547', '0.8916', '0.1804', '0.5024', '0.47', '0.10376', '-0.04944', '0.2229', '-0.2233', '0.2917', '-0.05594', '-0.3242', '0.01008']",C84594,,,250.80,,10024603,
mondo:0018884,Roch-Leri mesosomatous lipomatosis,['Roch-Leri syndrome'],,,529,C4274284,,,,,,,,
mondo:0018885,orbital leiomyoma,,,,52994,CN205236,,,,,,,,
mondo:0018888,congenital cornea plana,,,,53691,,"['-0.3062', '0.10065', '0.0763', '-0.03069', '0.255', '-0.1804', '-0.01002', '0.1534', '-0.2076', '-0.3308', '-0.0877', '-0.03093', '-0.2025', '0.1271', '-0.1962', '-0.1107', '0.2264', '-0.3262', '0.2566', '-0.539', '-0.1798', '0.1394', '0.2515', '0.02573', '0.1084', '0.05133', '0.02821', '0.1415', '0.106', '0.182', '0.2605', '0.0322', '-0.2036', '0.209', '0.03943', '0.02617', '-0.11993', '-0.232', '0.1293', '-0.187', '0.3057', '-0.11536', '-0.1007', '-0.014626', '-0.0799', '0.04205', '-0.0573', '0.02512', '0.207', '0.04834', '0.337', '0.01741', '-0.09265', '-0.3733', '-0.05154', '-0.3782', '0.1792', '0.02553', '-0.3315', '-0.3726', '0.11743', '-0.03723', '-0.2988', '0.07806', '0.002066', '-0.2457', '0.557', '0.479', '-0.0997', '0.2302', '-0.123', '0.2798', '0.2104', '-0.1874', '0.1632', '0.1686', '0.07947', '0.1179', '0.1606', '-0.2388', '-0.1478', '-0.0926', '0.0618', '0.4854', '-0.1506', '-0.1599', '-0.0223', '0.1217', '0.11694', '0.2554', '-0.04175', '0.516', '0.2062', '0.0714', '0.543', '-0.232', '0.2277', '-0.2708', '-0.08124', '0.0439']",,,,,,,
mondo:0018889,hyaline body myopathy,['myosin storage myopathy'],0111267,,53698,,"['-0.1219', '0.0896', '-0.0175', '-0.04886', '0.0456', '-0.1292', '-0.005077', '0.0744', '-0.1296', '-0.03635', '-0.06433', '0.012665', '0.02747', '0.02103', '-0.0322', '-0.007244', '-0.03497', '-0.05313', '-0.06146', '-0.2289', '0.004963', '-0.0615', '0.05414', '-0.005066', '0.01018', '-0.008865', '-0.0387', '-0.00494', '-0.02939', '-0.014656', '0.1086', '-0.01099', '0.0696', '0.01019', '0.0551', '0.00948', '-0.04248', '-0.02425', '0.01839', '-0.1279', '-0.0145', '-0.1111', '-0.00271', '0.01539', '0.013756', '-0.0923', '-0.007732', '0.1008', '0.00494', '0.02612', '-0.0396', '0.02116', '0.071', '0.02556', '-0.0736', '-0.1089', '0.12317', '-0.04175', '-0.08887', '-0.01489', '0.08655', '0.00813', '-0.00079', '-0.01952', '-0.05676', '0.002821', '0.1075', '0.09436', '-0.10144', '0.09357', '-0.09546', '-0.01953', '0.00925', '-0.04062', '-0.0269', '0.0858', '-0.02838', '0.03714', '-0.02159', '-0.0841', '0.03397', '0.00877', '0.0294', '0.10834', '0.02263', '-0.01682', '-0.0326', '0.09454', '0.0701', '0.0154', '0.1098', '0.10425', '0.0369', '0.03534', '0.1487', '0.0742', '0.09717', '-0.0983', '0.0197', '0.03018']",,,,,,,
mondo:0018890,Lyell syndrome,,,,537,CN205258,,,,,,,,
mondo:0018891,familial tumoral calcinosis,,,,53715,,"['-0.3674', '0.0565', '-0.2479', '-0.1852', '0.0922', '-0.4592', '-0.323', '0.6304', '-0.46', '0.4885', '0.2252', '0.267', '-0.07416', '0.1835', '-0.1921', '0.006454', '-0.07965', '0.07214', '0.123', '-0.2969', '0.0703', '-0.1239', '0.919', '-0.03577', '-0.006012', '0.2668', '0.0757', '-0.1458', '-0.4385', '-0.5103', '0.1334', '-0.6455', '0.2598', '-0.1924', '0.02693', '0.01857', '-0.2391', '-0.0293', '-0.06125', '-0.4624', '0.2075', '-0.672', '0.3643', '0.02187', '0.043', '0.1847', '0.0884', '0.1299', '-0.2448', '0.02231', '0.1998', '-0.3086', '0.4414', '0.3772', '-0.4868', '-0.4712', '0.04996', '0.0963', '-0.7017', '0.0903', '0.69', '-0.0834', '-0.933', '-0.2284', '-0.0316', '-0.2715', '0.3875', '0.43', '-0.2021', '0.02348', '0.0952', '-0.1696', '-0.0967', '-0.1316', '0.358', '0.2393', '-0.443', '0.5054', '-0.3025', '-0.4485', '-0.2852', '0.2205', '0.4175', '0.05093', '-0.2627', '-0.2498', '-0.086', '0.00951', '-0.316', '-0.1897', '0.1956', '0.4094', '0.1636', '-0.2832', '0.646', '-0.0873', '0.609', '-0.474', '-0.777', '-0.0857']",,,,,,10059364,
mondo:0018892,Wyburn-Mason syndrome,"['bonnet-Decaume-Blanc syndrome', 'CAMS2', 'Cerebrofacial arteriovenous metameric syndrome type 2', 'Wyburn Mason syndrome', 'bonnet-Dechaume-Blanc syndrome', 'Wyburn Mason^s syndrome', 'arteriovenous aneurysm of mid-brain and retina, facial nevi and mental changes']",,,53719,C0265321,,,,C536752,,,10048661,
mondo:0018893,Cobb syndrome,"['SAMS 1-31', 'Cobb^s syndrome', 'spinal arteriovenous metameric syndrome', 'cutaneomeningospinal angiomatosis']",,,53721,C0346068,,C4485,,,239.2,,10068841,
mondo:0018894,distal hereditary motor neuropathy,"['dSMA', 'dHMN', 'distal spinal muscular atrophy']",,,53739,,,,,,,,,
mondo:0018895,Plummer-Vinson syndrome,"['dysphagia sideropenica', 'Paterson-Brown-Kelly syndrome', 'Kelly^s syndrome', 'Paterson’s syndrome', 'Kelly-Paterson syndrome', 'Paterson-Kelly syndrome', 'Plummer Vinson syndrome', 'Paterson^s syndrome', 'Sideropenic dysphagia']",,,54028,C0032249,,C85016,,D011004,280.8,,10040664,
mondo:0018896,thrombotic thrombocytopenic purpura,"['TTP', 'Moschowitz disease', 'Moschcowitz disease', 'Moschcowitz^s syndrome']",10772,,54057,C0034155,,C78797,,D011697,,,10043648,
mondo:0018897,primary cutaneous CD30+ T-cell lymphoproliferative disease,['primary cutaneous Ki-1+ T-cell lymphoproliferative disease'],,,541,CN205268,,,,,,,10065863,
mondo:0018898,primary cutaneous lymphoma,"['primary cutaneous lymphoma', 'primary skin lymphoma', 'cutaneous (skin) lymphoma']",,,542,C1302772,,C7162,,,,,10051708,
mondo:0018899,posterior cortical atrophy,"['biparietal Alzheimer disease', 'PCA', 'Benson syndrome']",,,54247,CN205270,,,,,,,,
mondo:0018900,corticosteroid-sensitive aseptic abscess syndrome,"['aseptic abscesses syndrome', 'corticosteroid-sensitive aseptic abscesses', 'aseptic systemic abscesses', 'disseminated aseptic abscesses']",,,54251,CN205271,,,,,,,,
mondo:0018901,left ventricular noncompaction,"['LVNC', 'spongy myocardium', 'left ventricular non-compaction cardiomyopathy', 'left ventricular non-compaction syndrome', 'Lv non-compaction syndrome', 'left ventricular noncompaction (disease)', 'left ventricular hypertrabeculation']",0060480,,54260,C4021133,"['-0.464', '-0.08746', '0.1289', '-0.0336', '0.00104', '-0.1918', '0.07965', '0.5405', '-0.11224', '0.09033', '-0.1023', '-0.3757', '-0.1798', '-0.2195', '-0.8755', '-0.503', '-0.536', '-0.12146', '-0.1986', '-0.657', '0.253', '0.3167', '0.408', '0.2834', '0.1177', '-0.1014', '0.0386', '0.2128', '0.0465', '0.2498', '0.32', '0.02647', '0.1077', '0.3438', '0.01819', '-0.4102', '0.1544', '0.2142', '0.3267', '-0.5415', '0.2426', '-0.0946', '0.241', '0.3809', '-0.1338', '0.3088', '-0.455', '0.3809', '-0.0812', '-0.03772', '-0.1676', '0.1821', '0.1292', '0.0192', '-0.176', '-0.1729', '0.3167', '-0.1103', '-0.52', '0.014854', '-0.0671', '0.2915', '-0.11774', '-0.1144', '-0.1168', '-0.1919', '0.5566', '0.473', '-0.1659', '0.4482', '-0.356', '-0.05765', '0.4363', '0.0879', '-0.5977', '-0.04324', '0.1881', '-0.2029', '-0.04758', '-0.1647', '0.03433', '-0.2559', '0.2502', '-0.0567', '0.005978', '0.05905', '-0.1349', '0.329', '0.1552', '-0.1117', '0.162', '-0.0108', '0.2195', '0.1838', '0.6343', '0.3257', '0.5654', '-0.3945', '-0.3667', '0.3396']",C99544,,,,,,
mondo:0018902,hepatocellular adenoma,"['adenoma, hepatocellular, benign', 'liver cell adenoma', 'adenoma of the liver cells', 'hepatocellular adenoma', 'adenoma of liver cells', 'HCA', 'LIAD']",0050868,,54272,C0206669,"['-0.4229', '-0.1943', '-0.8047', '0.225', '0.2042', '-0.02176', '0.2192', '0.5376', '-0.1936', '0.0716', '0.04526', '0.1768', '-0.2656', '0.31', '-0.4546', '-0.2328', '0.03006', '-0.2742', '0.3164', '-0.5796', '-0.06445', '-0.09314', '0.723', '-0.12103', '0.04968', '-0.01814', '-0.2612', '0.0899', '-0.264', '0.1768', '0.87', '-0.333', '0.2214', '-0.1857', '-0.4866', '-0.1096', '-0.5176', '-0.2874', '0.506', '-0.09454', '0.2961', '-0.3308', '0.1603', '-0.3784', '0.2979', '0.6084', '-0.2793', '-0.224', '-0.2157', '-0.02461', '0.2389', '0.1431', '-0.3435', '0.2666', '-0.648', '0.0913', '0.654', '0.003462', '-0.7153', '0.579', '0.3162', '0.5537', '-0.354', '-0.02072', '-0.2507', '-0.136', '0.2461', '0.52', '-0.1948', '0.87', '0.174', '0.402', '0.05734', '-0.3245', '0.332', '-0.0152', '0.141', '-0.04797', '-0.3577', '-1.325', '-0.619', '0.1622', '0.07916', '-0.408', '-0.15', '-0.1676', '-0.04318', '-0.12146', '0.00718', '-0.697', '0.4854', '0.04907', '-0.6025', '-0.1637', '0.442', '0.03998', '0.2866', '-0.3733', '-0.4932', '0.125']",C3758,0000762,D018248,,,10019827,
mondo:0018903,sarcocystosis,['sarcosporidiosis'],9640,,54368,C0036231,,,0007476,D012523,136.5,,10039483,
mondo:0018904,primary membranoproliferative glomerulonephritis,"['Mesangiocapillary glomerulonephritis', 'MPGN', 'membranoproliferative glomerulonephritis']",,,54370,C0017662,"['0.7046', '0.343', '-0.4302', '0.394', '-0.185', '-0.312', '0.10913', '-0.1506', '-0.5073', '-0.0408', '0.3286', '-0.1179', '-0.4128', '0.8276', '-0.1111', '-0.365', '-0.1262', '0.4077', '0.7', '-0.12317', '-0.08527', '-0.8423', '0.7266', '0.0836', '0.552', '-0.0785', '-0.9956', '0.806', '0.0986', '-0.2273', '0.3687', '0.0983', '0.7773', '0.0434', '-0.10693', '-0.2756', '-0.3708', '0.993', '0.3757', '-0.5107', '-0.2351', '-0.2732', '-0.05875', '-0.536', '0.1897', '-0.2705', '-0.3782', '-0.2424', '-0.1746', '-0.06046', '0.3728', '0.1715', '1.279', '-0.576', '-0.4988', '-0.3604', '0.136', '-0.2113', '-0.7104', '-0.5244', '-0.887', '0.299', '0.08875', '-0.0889', '-0.07385', '-0.4746', '0.3716', '0.4167', '-0.73', '0.5103', '-0.796', '0.2585', '0.3872', '-0.2211', '0.0894', '0.066', '0.3801', '1.079', '-0.1606', '0.38', '-0.2076', '0.053', '0.2424', '0.1436', '0.1229', '-0.391', '0.2795', '-0.2257', '-0.000742', '0.812', '0.6313', '0.364', '-0.5703', '-0.04724', '0.5884', '0.7124', '-0.07654', '-0.56', '-0.786', '0.06573']",,,,583.2,,10018370,
mondo:0018905,diffuse large B-cell lymphoma,"['diffuse large B-cell lymphoma', 'DLBCL']",0050745,,544,C0079744,,C8851,0000403,D016403,200.7,,10012818,
mondo:0018906,follicular lymphoma,"['lymphoma, follicular', 'follicle centre lymphoma', 'follicular non-Hodgkin lymphoma', 'follicular center cell lymphoma', 'follicular non-Hodgkin^s lymphoma', 'lymphoma, follicular centre cell', 'follicular centre cell lymphoma', 'lymphoma, follicular center cell', 'follicle center lymphoma', 'lymphoma, follicular, malignant']",0050873,,545,C0024301,,C3209,,D008224,,,,
mondo:0018907,craniopharyngioma,"['tumour of Rathke^s pouch', 'Adamantinomatous tumour', 'Rathke pouch neoplasm', 'Rathke pouch tumor', 'tumor of Rathke^s pouch', 'Rathke^s pouch neoplasm', 'craniopharyngioma (morphologic abnormality)', 'Rathke^s pouch tumor', 'Dysodontogenic epithelial tumor', 'Adamantinomatous tumor', 'cystoma', 'craniopharyngioma, benign', 'craniopharyngeal duct tumor', 'craniopharyngeal duct tumour', 'Rathke^s pouch tumour', 'Rathke pouch tumour', 'craniopharyngioma (WHO grade I)', 'neoplasm of Rathke^s pouch', 'Dysodontogenic epithelial tumour']",3840,,54595,C0010276,,C2964,1000209,D003397,237.0,,10011318,
mondo:0018908,non-Hodgkin lymphoma,"['non-Hodgkins lymphoma', 'non-Hodgkin^s lymphoma', 'NHL', 'non-Hodgkin lymphoma', 'non-Hodgkin^s lymphoma (NHL)']",0060060,,547,C0024305,,C3211,0005952,D008228,,,10029547,
mondo:0018910,oculocutaneous albinism,"['nonsyndromic oculocutaneous albinism', 'OCA', 'albinism, oculocutaneous']",0050632,,55,C0078918,,C84941,,D016115,270.2,,,
mondo:0018911,maturity-onset diabetes of the young,"['Mason type diabetes', 'maturity onset diabetes of the young', 'maturity-onset diabetes of the young', 'maturity-onset diabetes of the young (disease)', 'Mason-type diabetes', 'MODY']",0050524,606391,552,C0342276,"['0.7646', '-0.176', '0.05396', '0.734', '-0.335', '-0.869', '-0.2113', '0.91', '0.138', '-0.5176', '0.1237', '-0.2815', '0.3833', '0.1364', '-0.9224', '-0.4512', '0.2876', '0.12335', '0.09216', '-0.5293', '0.2217', '-0.2615', '0.1182', '0.1514', '-0.528', '-0.2554', '0.1002', '0.08124', '0.4883', '-0.3518', '1.028', '-0.4956', '0.07007', '0.09283', '0.069', '0.3806', '-0.6445', '0.505', '0.01383', '-0.289', '0.07855', '0.3398', '0.2416', '0.1434', '-0.1731', '-0.5034', '0.389', '-0.1371', '0.1453', '0.3013', '0.2576', '-0.503', '0.82', '-0.653', '-0.02347', '0.1345', '0.03864', '-0.836', '-0.885', '0.3394', '-0.4067', '0.557', '-0.1122', '0.1755', '0.05194', '0.8257', '-0.527', '0.595', '-0.889', '0.515', '0.3066', '0.2484', '0.05673', '-0.1278', '0.6187', '0.538', '-0.569', '0.9067', '-0.3853', '-0.1157', '0.02292', '-0.0457', '0.10205', '-0.5317', '0.2257', '0.1771', '0.02054', '0.4067', '0.826', '0.1401', '0.6094', '0.2854', '-0.1562', '-0.273', '1.213', '0.2595', '-0.2898', '-0.1752', '-0.4019', '0.05807']",C114769,,C562772,,,,0004904
mondo:0018912,Cushing syndrome,"['suprarenogenic syndrome', 'ectopic adrenocorticotropic hormone syndrome', 'cortisol Excess', 'hypercortisolism', 'Cushing^s syndrome', 'nodular primary adrenocortical dysplasia', 'pituitary basophilism', 'Cushing syndrome', 'adrenal hyperfunction resulting from pituitary ACTH excess', 'hyperadrenocorticism']",,,553,C0010481,"['-0.1989', '0.3813', '-0.2708', '-0.7227', '0.0794', '0.381', '0.02551', '0.5625', '-0.533', '0.2532', '0.02206', '0.1313', '0.1359', '0.942', '-0.3555', '0.2153', '-0.1438', '0.603', '-0.12286', '-0.5327', '-0.076', '-0.831', '0.54', '-0.2335', '-0.304', '0.2137', '-0.1416', '-0.333', '0.01318', '0.3342', '0.2095', '-0.1427', '0.263', '-0.2362', '-0.3', '0.5156', '-0.4324', '0.1207', '0.08014', '-0.3618', '0.5195', '0.1255', '-0.2043', '-0.567', '0.8394', '-0.3638', '-0.1161', '-0.2018', '0.4795', '0.515', '-0.182', '0.5537', '0.403', '0.01128', '-0.6035', '-0.05533', '0.596', '-0.4885', '-0.6274', '0.0856', '0.02383', '0.951', '-0.624', '-0.02017', '-0.3535', '0.618', '-0.567', '0.3064', '-0.59', '0.6475', '-0.1144', '0.1785', '0.0654', '-0.088', '0.07495', '0.336', '-0.0608', '-0.02197', '0.7676', '-0.3704', '0.01639', '-0.09424', '-0.12445', '-0.2996', '-0.525', '0.2457', '0.324', '-0.09314', '0.725', '0.2666', '0.261', '0.2712', '0.1984', '-0.2396', '0.3381', '-0.2747', '-0.1704', '0.4326', '-0.0721', '0.4463']",C2969,0003099,D003480,255.0,E24,10020610,
mondo:0018913,malakoplakia,['malacoplakia'],,,556,,,C84833,1001807,D008287,,,,
mondo:0018914,hypotrichosis simplex,['hereditary hypotrichosis simplex'],,,55654,C1854310,"['-0.1843', '-0.011185', '-0.596', '-0.02055', '0.913', '-0.7837', '-0.2096', '0.4033', '-0.18', '-0.609', '-0.343', '-0.1667', '-0.4854', '-0.04147', '-0.3113', '0.4617', '0.7705', '-0.302', '-0.845', '-0.6562', '-0.7515', '-0.1954', '0.1274', '-0.0852', '0.5054', '0.3135', '-0.4473', '0.125', '0.2698', '-0.2188', '0.9565', '-0.11304', '-0.06033', '-0.02704', '0.849', '0.02994', '-0.1956', '-0.5806', '0.02426', '0.014046', '0.3105', '-0.001176', '0.03128', '-0.573', '0.1407', '-0.2913', '0.01131', '-0.14', '0.097', '-0.0746', '0.5547', '-0.587', '0.7153', '0.02597', '-0.3965', '-0.516', '0.5483', '-0.10297', '-0.1757', '-0.1947', '-0.3857', '-0.4304', '0.504', '-0.1771', '-0.1699', '-0.1282', '-0.0374', '0.6147', '-0.496', '0.9062', '-0.01428', '-0.6704', '-0.07715', '0.2637', '0.10376', '0.4346', '-0.5127', '0.2432', '0.11865', '-0.2307', '0.54', '0.0883', '0.5957', '0.1495', '0.03568', '0.10864', '-0.1482', '0.06088', '0.6357', '0.1604', '0.02734', '0.6855', '0.4832', '0.5146', '0.7153', '-0.0383', '0.3367', '-0.1268', '0.6816', '0.2007']",,,C537160,,,,
mondo:0018916,isolated anorectal malformation,['nonsyndromic anorectal malformation'],,,557,,,,,,,,,
mondo:0018918,carcinoma of gallbladder and extrahepatic biliary tract,['carcinoma of gallbladder and EBT'],,,56044,CN205299,,,,,,,10007426,
mondo:0018919,McCune-Albright syndrome,"['PFD', 'mccune-albright syndrome, somatic, mosaic', 'POFD', 'Albright^s disease', 'gonadotropin-independent female-limited sexual precocity', 'polyostotic fibrous dysplasia', 'McCune Albright syndrome', 'MAS']",1858,174800,562,C0242292,"['-0.0906', '-0.383', '0.0735', '-0.5693', '0.7803', '-0.2207', '0.4282', '0.862', '-0.7476', '-0.4373', '-0.4937', '0.0909', '-0.1141', '0.9624', '-0.2751', '-0.2201', '-0.3752', '-0.2015', '-0.548', '-0.3157', '0.279', '-0.34', '0.7954', '-0.2477', '0.254', '-0.0878', '0.2878', '-0.674', '-0.0311', '0.01816', '0.622', '-0.375', '0.367', '0.188', '-0.11273', '-0.3044', '-0.01563', '0.2008', '-0.06235', '0.1742', '0.529', '-0.04517', '0.4487', '-0.05136', '0.765', '-0.1982', '-0.2213', '-0.05536', '0.5337', '0.1344', '0.04715', '0.2595', '0.09656', '0.2888', '-0.1775', '-0.2507', '0.455', '-0.376', '-0.762', '-0.1466', '0.9326', '0.1611', '-0.141', '0.1633', '0.283', '0.4255', '0.6', '0.499', '0.5947', '-0.3496', '0.1322', '-0.758', '-0.2502', '0.406', '-0.0699', '-0.3584', '0.2094', '0.518', '0.03494', '-0.5586', '0.1711', '-0.1498', '-0.3613', '-0.1423', '-0.635', '-0.2764', '0.4048', '0.0654', '0.03317', '0.01872', '-0.04745', '0.38', '-0.0683', '0.0377', '0.478', '-0.058', '0.4314', '-0.534', '0.4585', '-0.0726']",C48627,,D005359,,Q78.1,,
mondo:0018920,peripartum cardiomyopathy,"['peripartum cardiomyopathy', 'antepartum peripartum cardiomyopathy', 'postpartum peripartum cardiomyopathy', 'Meadows^ syndrome', 'postpartum cardiomyopathy']",9997,,563,C0269972,,C171602,0002628,,674.54,O90.3,10049430,
mondo:0018921,Meckel syndrome,['Meckel-Gruber syndrome'],0050778,,564,C0265215,"['-0.02425', '-0.1909', '0.1114', '-0.338', '0.2595', '-0.519', '-0.3596', '0.7974', '-0.7', '-0.4487', '-0.7686', '-0.9336', '-0.29', '0.1333', '-0.3142', '-0.3164', '0.0005918', '-0.267', '-0.6245', '-0.807', '-0.225', '0.2837', '1.319', '-0.6147', '-0.4912', '-0.73', '-0.1724', '-0.03592', '0.9272', '-0.11224', '0.825', '-0.1906', '0.4197', '0.06726', '0.385', '-0.214', '-0.2065', '-0.2357', '0.01697', '0.0979', '-0.1929', '0.04834', '-0.00478', '-0.1906', '-0.1825', '-0.3667', '0.2482', '0.5767', '-0.1943', '0.1023', '-0.04047', '0.1495', '-0.08923', '-0.361', '-0.3877', '0.259', '-0.01653', '-0.3652', '-0.261', '-0.12195', '0.376', '0.3594', '0.2124', '0.2463', '-0.7104', '-0.6143', '0.605', '-0.4006', '-0.675', '0.277', '-0.4197', '0.2471', '-0.06793', '0.805', '-0.214', '-0.1432', '0.5215', '-0.01791', '-0.617', '-0.532', '-0.4304', '0.01515', '0.3857', '0.4219', '-0.3054', '-0.3755', '0.976', '0.2517', '-0.7803', '0.04657', '0.3154', '0.12115', '0.469', '-0.09406', '0.7583', '-0.1355', '0.3616', '-0.304', '0.06586', '-0.03946']",C98978,,,759.89,,,
mondo:0018922,cold agglutinin disease,"['chronic cold agglutinin disease', 'cold antibody disease', 'CAD', 'cold agglutinin syndrome', 'CAS', 'cold antibody hemolytic anemia', 'cold antibody hemolytic anaemia', 'anemia, hemolytic, cold antibody']",,,56425,CN205305,,,,,,,,
mondo:0018923,22q11.2 deletion syndrome,"['Takao syndrome', 'Cayler cardiofacial syndrome', 'Shprintzen syndrome', 'conotruncal anomaly face syndrome', 'VCFS', 'Sedlackova syndrome', 'DiGeorge syndrome', 'velocardiofacial syndrome', 'microdeletion 22q11.2', 'DiGeorge sequence', '22q11DS', 'catch 22', 'monosomy 22q11']",,,567,,"['0.09', '-0.0981', '-0.00308', '-0.054', '-0.0102', '0.0478', '0.3152', '0.8525', '-0.8506', '-0.658', '0.4094', '-0.5547', '0.1204', '0.445', '-0.1576', '-0.1471', '-0.942', '-0.128', '-0.9087', '-0.492', '0.276', '0.1199', '0.3152', '-0.254', '0.4448', '-0.3167', '-0.0841', '-0.2166', '0.615', '-0.1643', '0.3337', '-0.3987', '0.1362', '0.0335', '-0.4233', '0.225', '-0.1738', '0.15', '-0.05475', '-0.2291', '0.728', '1.124', '-0.155', '-0.3923', '-0.3293', '-0.3523', '0.3484', '0.09235', '0.083', '-0.159', '-0.5444', '0.01746', '-0.591', '-0.003742', '-0.7407', '-0.3862', '-0.653', '0.1395', '-0.126', '-0.02092', '-0.01173', '0.5015', '0.03026', '0.778', '0.2693', '0.5938', '0.07605', '0.05066', '-1.011', '0.693', '-0.0621', '-0.2542', '-0.1946', '-0.495', '0.03696', '0.1477', '0.3408', '-0.0707', '-0.2935', '-0.001433', '0.6055', '-0.2544', '-0.07477', '-0.01102', '-0.0443', '-0.3667', '0.193', '0.3896', '0.5757', '0.3801', '0.07983', '0.5166', '-0.1213', '-0.1624', '0.2854', '-0.07544', '-0.3296', '-0.0937', '0.136', '0.3887']",,,,,,10066430,
mondo:0018924,"microphthalmia, Lenz type","['microphthalmia or anophthalmos with associated anomalies (formerly)', 'syndromic microphthalmia type 1', 'Lenz microphthamia syndrome', 'microphthalmia syndromic 1', 'Lenz microphthalmia', 'MCOPS1', 'microphthalmia Lenz type', 'Lenz dysplasia', 'MAA (formerly)']",,,568,,,,,,,,,
mondo:0018925,familial or sporadic hemiplegic migraine,['hemiplegic migraine'],,,569,,,,,,346.30,,,
mondo:0018926,human prion disease,"['transmissible spongiform encephalopathy', 'TSE']",,,56970,,,,,,,A81.1,,
mondo:0018927,SUNCT syndrome,"['short-lasting unilateral neuralgiform headache attacks with conjunctival injection and tearing', 'short-lasting, unilateral, neuralgiform headache attacks with conjunctival injection and tearing', 'SUNCT headache']",,,57145,C1262087,,C85174,,D050798,,,10061981,
mondo:0018929,medial condensing osteitis of the clavicle,"['condensing osteitis of the clavicle', 'osteitis condensans of the clavicle', 'condensing osteitis of the medial clavicle']",,,57196,CN230280,,,,,,,,
mondo:0018930,monosomy 21,"['21q deletion syndrome', 'deletion 21q', '21q- syndrome', '21q deletion', 'monosomy type 21', 'chromosome 21q deletion', 'monosomy 21q', 'partial 21q monosomy', 'partial monosomy 21q', '21q monosomy']",,,574,C0795875,,C36469,,C537108,,,,
mondo:0018931,"mucolipidosis type III, alpha/beta","['MLIII', 'mucolipidosis 3A', 'mucolipidosis III', 'mucolipidosis 3 Alpha/Beta, atypical', 'ML3', 'mucolipidosis III ALPHA/BETA', 'ML 3', 'ML 3 Alpha/Beta', 'mucolipidosis 3', 'ML III alpha/beta', 'ML 3 A', 'pseudo-Hurler polydystrophy', 'mucolipidosis type III alpha/beta', 'mucolipidosis type 3 alpha/beta', 'mucolipidosis 3 Alpha/Beta', 'ML 3 alpha/beta', 'mucolipidosis type 3A', 'mucolipidosis type III']",0080071,252600,577,CN237499,"['0.192', '-0.01439', '0.1884', '-0.07294', '-0.1026', '-0.675', '0.6587', '1.415', '-0.325', '0.1576', '-0.3577', '0.8726', '-0.2825', '0.314', '-0.308', '-0.1683', '-0.11597', '-0.3167', '-0.633', '-0.2827', '0.1205', '0.3418', '0.5005', '0.0806', '-0.3022', '-0.792', '0.3958', '0.375', '0.004135', '0.1655', '0.359', '0.10284', '0.1162', '0.325', '-0.2194', '-0.798', '0.05597', '-0.534', '0.3179', '-0.1985', '-0.1416', '-0.1844', '0.1293', '0.6616', '-0.05698', '0.6606', '-0.1492', '0.3203', '-0.3735', '0.211', '0.2134', '-0.1272', '0.3281', '-0.02426', '0.01381', '-0.0739', '-0.02629', '0.11224', '0.10657', '0.1627', '0.1741', '0.2979', '-0.3088', '0.0938', '0.06064', '-0.0728', '0.1268', '0.4094', '-0.1074', '0.1428', '-0.3762', '0.01726', '-0.4592', '-0.5645', '-0.1384', '-0.1282', '-0.02798', '-0.1389', '-0.5405', '-0.3657', '-0.4182', '-0.197', '-0.8374', '0.405', '-0.2603', '0.623', '-0.326', '-0.0348', '0.5225', '-0.0391', '0.04227', '0.3728', '-0.431', '0.1326', '0.2979', '0.1072', '0.502', '-0.6987', '0.58', '-0.02357']",,,,,,,
mondo:0018932,cirrhotic cardiomyopathy,,,,57777,C4511053,,,,,,,,
mondo:0018933,Mazabraud syndrome,['Myxoma with fibrous dysplasia'],,,57782,CN205323,,,,,733.29,,,
mondo:0018935,hairy cell leukemia,"['HCL', 'leukemic reticuloendotheliosis', 'HCL-C', 'classic hairy cell leukaemia', 'classic hairy cell leukemia', 'hairy cell leukemia']",285,,58017,C0023443,,C7402,1000956,D007943,202.4,,10019055,
mondo:0018936,osteoblastoma,"['osteoblastoma, benign', 'giant osteoid osteoma', 'ossifying giant cell tumor', 'ossifying giant cell tumour', 'osteoblastoma (disease)', 'osteoblastoma']",0060098,,58040,C0029417,,C3294,1000410,D018215,,D16.5,10004430,0011846
mondo:0018937,mucopolysaccharidosis type 3,"['N-acetyl-alpha-D-glucosaminidase deficiency', 'MPS IIIC - Sanfilippo syndrome C', 'MPS IIIB - Sanfilippo syndrome B', 'Sanfilippo syndrome B', 'Sanfilippo syndrome', 'mucopolysaccharidosis III', 'NAGLU deficiency', 'mucopolysaccharidosis type III', 'MPS3', 'heparan sulphate sulfatase deficiency', 'MPSIII', 'Sanfilippo syndrome A', 'Sanfilippo disease', 'MPS IIID - Sanfilippo syndrome D', 'mucopolysaccharidosis, MPS-III-B', 'Sanfilippo^s syndrome', 'N-sulphoglucosamine sulphohydrolase deficiency', 'mucopolysaccharidosis, MPS-III', 'MPS IIIA - Sanfilippo syndrome A', 'Mucopoly-saccharidosis type 3', 'heparan sulfate sulfatase deficiency', 'mucopolysaccharidosis type IIIB', 'mucopolysaccharidosis type IIIA']",12801,,581,CN205330,"['0.2693', '0.2766', '-0.0767', '0.0482', '-0.03772', '-0.3704', '0.1473', '0.5034', '-0.398', '0.3245', '-0.0794', '0.2485', '-0.1934', '0.4802', '0.2191', '0.03632', '0.03442', '-0.0782', '-0.3064', '-0.09814', '-0.02267', '-0.1251', '0.896', '-0.1611', '-0.09644', '-0.1272', '-0.2622', '-0.4827', '-0.6807', '0.004715', '0.582', '0.0903', '0.2937', '-0.00721', '-0.12', '-0.363', '-0.249', '-0.536', '0.04562', '0.0953', '-0.3691', '-0.2834', '0.3113', '0.5264', '0.218', '-0.1004', '-0.3105', '0.0982', '-0.1497', '-0.1388', '-0.00446', '-0.1913', '-0.1931', '0.01578', '0.675', '-0.1952', '-0.2034', '-0.152', '0.0402', '0.0763', '0.1262', '-0.0863', '0.1793', '-0.2168', '-0.1283', '-0.3914', '0.295', '-0.4844', '-0.3633', '0.2886', '-0.3171', '-0.559', '0.0874', '-0.3572', '0.5645', '0.516', '-0.00416', '-0.2203', '-0.2288', '-0.2874', '-0.05182', '-0.7417', '-0.5376', '0.583', '-0.06866', '0.3364', '0.541', '0.638', '0.562', '0.5044', '0.06235', '0.436', '-0.1774', '-0.01043', '0.2578', '0.5522', '0.0394', '-0.4492', '0.6143', '-0.089']",C61262,,,,,10056890,
mondo:0018938,mucopolysaccharidosis type 4,"['Morquio A disease', 'Osteochondrodystrophy', 'galactosamine-6-sulfatase deficiency', 'deficiency of chondroitinsulphatase', 'Morquio disease', 'mucopolysaccharidosis IV', 'mucopolysaccharidosis type IVB', 'Morquio syndrome A', 'MPS4', 'MPSIV', 'mucopolysaccharidosis type IVA', 'Morquio syndrome', 'mucopolysaccharidosis type 4', 'mucopolysaccharidosis, MPS-IV-A', 'MPS IV - Morquio syndrome A', 'MPS IV - Morquio syndrome B', 'mucopolysaccharidosis type IV', 'chondroosteodystrophy', 'deficiency of N-acetylgalactosamine-6-sulphatase', 'mucopolysaccharidosis, MPS-IV']",12804,,582,C0026707,"['-0.2737', '-0.01595', '-0.02992', '-0.1427', '0.3062', '-0.4377', '0.524', '0.7197', '-0.918', '-0.1416', '-0.1556', '0.139', '0.1869', '0.2515', '-0.1076', '-0.4631', '0.2698', '-0.1981', '-0.1569', '-0.2285', '0.0241', '0.02759', '1.059', '-0.1664', '-0.1378', '-0.3877', '0.1478', '0.2607', '-0.53', '0.0668', '0.6284', '0.3345', '0.519', '0.1787', '0.155', '-1.024', '0.2094', '-0.596', '0.1407', '0.3599', '-0.01059', '-0.07166', '0.891', '0.502', '-0.2314', '0.481', '0.1528', '-0.1813', '-0.1212', '0.1572', '0.0471', '0.1084', '0.2725', '0.014015', '0.1576', '-0.7344', '-0.3027', '0.0947', '0.106', '0.0954', '0.1658', '0.2854', '-1.15', '0.01447', '-0.1622', '-0.326', '0.1127', '-0.0010395', '-0.1267', '0.10516', '-0.0593', '0.2322', '-0.0644', '-0.196', '0.3682', '0.2332', '-0.0833', '0.2593', '-0.3447', '0.008064', '-0.8193', '-0.11365', '-0.2935', '0.9316', '-0.4795', '0.5347', '0.1235', '0.1638', '0.8154', '-0.08746', '-0.10443', '-0.0469', '-0.2476', '0.01643', '0.2551', '0.4143', '0.2087', '-0.2423', '0.2598', '0.01032']",C61263,,,,,10028095,
mondo:0018939,muscle-eye-brain disease,"['Santavuori congenital muscular dystrophy', 'muscle eye brain disease', 'muscular dystrophy-dystroglycanopathy congenital with brain and eye anomalies A3', 'MEB', 'MEB syndrome', 'muscle-eye-brain syndrome']",,,588,,,,,,742.4,,,
mondo:0018940,congenital myasthenic syndrome,"['familial limb-girdle myasthenia', 'erb-Goldflam syndrome', 'myasthenia gravis pseudoparalytica', 'CMS', 'myasthenic syndrome, congenital', 'myasthenia gravis congenital', 'congenital MG', 'congenital myasthenia']",3635,,590,C0751882,"['-0.331', '0.0741', '0.1981', '-0.2864', '0.2588', '-0.3562', '-0.07715', '0.3762', '-0.279', '-0.1251', '-0.3032', '-0.0627', '-0.1493', '0.1555', '0.1132', '0.4575', '-0.277', '0.0736', '-0.179', '-0.618', '0.2551', '0.2668', '0.4521', '0.1879', '-0.272', '-0.2834', '0.2078', '-0.3633', '0.08325', '-0.1934', '0.278', '0.4521', '0.3306', '0.1266', '-0.1437', '0.02039', '-0.2622', '-0.02164', '-0.331', '-0.2913', '-0.05573', '-0.311', '-0.0794', '0.18', '0.02104', '-0.4229', '-0.05405', '0.313', '0.356', '0.4932', '-0.1559', '0.06226', '-0.0561', '-0.007004', '-0.03308', '-0.543', '0.05405', '0.3672', '-0.1504', '0.05438', '-0.0229', '-0.000358', '0.0582', '0.0809', '-0.2382', '0.06018', '0.10815', '0.1888', '-0.483', '0.3853', '-0.4878', '-0.05566', '-0.01188', '-0.1768', '0.4204', '-0.02885', '0.2351', '0.0316', '-0.1501', '-0.087', '0.2656', '-0.033', '0.07385', '0.1967', '-0.2341', '-0.05426', '0.2267', '0.435', '0.0226', '-0.1288', '0.2035', '0.269', '0.2517', '0.1355', '0.093', '0.3948', '0.382', '0.1243', '-0.0932', '0.1919']",C84647,,D020294,V17.89,,,
mondo:0018941,furuncular myiasis,"['furunculous myiasis', 'furunculoid myiasis']",,,591,C2931766,,,,C538194,,,,
mondo:0018942,macrophagic myofasciitis,"['MMF', 'Macrophagic myofasciitis, childhood']",,,592,C2931639,,,,C537829,,,,
mondo:0018943,myofibrillar myopathy,"['myofibrillar myopathy', 'desmin storage myopathy (former name)', 'filaminopathy (type)', 'myotilinopathy (type)', 'Alpha Beta crystallinopathy (type)', 'myofibrillar myopathies', 'Protein surplus myopathy (former name)', 'desmin related myopathy (former name)', 'Zaspopathy (type)', 'myofibrillar myopathy (disease)', 'Desminopathy (type)']",0080307,,593,C2678065,"['-0.2793', '-0.07916', '-0.03806', '-0.06244', '-0.1924', '-0.4421', '0.1405', '0.005493', '-0.6895', '0.007404', '-0.2695', '-0.1562', '0.0673', '0.1063', '-0.08795', '0.03473', '-0.5083', '-0.03186', '-0.12274', '-0.65', '0.3457', '0.005222', '0.5044', '0.1884', '-0.0706', '-0.1273', '0.0816', '-0.4834', '-0.1761', '0.02061', '0.3064', '0.0546', '0.0753', '0.000823', '0.07874', '-0.10547', '-0.1763', '0.2296', '0.114', '-0.2382', '-0.1704', '-0.7666', '-0.01271', '0.2969', '0.03442', '-0.2937', '-0.04184', '0.2124', '0.1891', '0.42', '-0.1209', '0.06866', '0.1969', '0.076', '-0.02274', '-0.5107', '0.3635', '0.145', '-0.06396', '0.1186', '0.3562', '-0.07574', '-0.04996', '0.00709', '-0.2708', '-0.3105', '0.2678', '0.4658', '-0.2927', '0.0736', '-0.1237', '-0.11273', '0.05682', '0.3335', '0.353', '0.3306', '-0.1365', '0.06506', '-0.179', '-0.1656', '-0.1392', '-0.1289', '0.32', '0.2566', '-0.065', '-0.005737', '-0.1533', '0.1262', '0.3035', '-0.2306', '0.325', '0.1476', '0.0688', '-0.1558', '0.2546', '0.3062', '0.421', '-0.197', '-0.1578', '-0.1048']",C83009,,C580316,359.89,,,0003715
mondo:0018944,gestational trophoblastic neoplasm,"['gestational trophoblastic tumor', 'gestational trophoblastic neoplasia', 'molar pregnancy', 'GTT', 'GTN', 'hydatidiform mole', 'gestational trophoblastic disease', 'gestational trophoblastic tumour']",3590,,59305,C1135868,,C4699,,D006828,630,,10061988,
mondo:0018945,McLeod neuroacanthocytosis syndrome,"['MCLDS', 'McLeod syndrome', 'McLeod syndrome with chronic granulomatous disease', 'mcleod syndrome with or without chronic granulomatous disease', 'McLeod phenotype', 'X-linked McLeod syndrome', 'MLS', 'neuroacanthocytosis, McLeod type']",0112107,300842,59306,,"['-0.3752', '0.4734', '-0.01773', '-0.1205', '-0.278', '-0.3972', '0.05124', '0.3408', '0.2383', '-0.704', '0.268', '-0.5137', '-0.081', '0.3044', '0.726', '-0.4893', '-0.2384', '-0.146', '-0.303', '-0.4087', '-0.1431', '0.2316', '0.1744', '-0.000969', '0.01174', '-0.1219', '0.2617', '-0.02364', '0.147', '0.0528', '0.6753', '0.006393', '0.7456', '-0.079', '-0.0714', '-0.3516', '-0.5894', '-0.3188', '-0.03702', '-0.4744', '0.628', '-0.5015', '-0.005356', '-0.2627', '0.88', '0.2825', '-0.4678', '0.2079', '-0.3015', '0.3428', '-0.0004818', '0.3015', '-0.05054', '-0.093', '0.505', '-0.1508', '-0.05133', '0.3665', '-0.357', '-0.08136', '0.0422', '-0.1893', '0.777', '-0.0522', '-0.7217', '0.4897', '0.02422', '0.592', '-0.8564', '0.1229', '-0.2188', '-0.386', '-0.09454', '0.2041', '0.5967', '-0.01932', '0.06183', '-0.1769', '0.0875', '-0.12415', '0.834', '-0.621', '0.1362', '0.0811', '-0.6665', '-0.04105', '0.2717', '-0.05966', '0.5073', '-0.09607', '0.2668', '-0.177', '0.02557', '0.2808', '0.2382', '0.5977', '-0.1605', '0.09863', '-0.1231', '-0.0903']",,,C564038,289.89,,,
mondo:0018946,rhombencephalosynapsis,,,,59315,C1866130,,,,,742.4,,,
mondo:0018947,centronuclear myopathy,"['myotubular myopathy', 'CNM', 'myopathy, myotubular', 'myopathy, centronuclear']",14717,,595,C0175709,,C84648,,D020914,,,,
mondo:0018948,multiminicore myopathy,"['MmD', 'multicore myopathy', 'multicore disease', 'multiminicore disease']",0080991,,598,C0270962,,,,,,,,
mondo:0018949,distal myopathy,"['Miyoshi muscular dystrophy', 'distal myopathy', 'distal muscular dystrophy']",11720,,599,C0751336,"['-0.12463', '-0.1199', '-0.6426', '-0.1893', '0.445', '-1.273', '0.0951', '0.5957', '-1.031', '-0.388', '-0.0851', '0.361', '0.01894', '0.4893', '-0.03357', '-0.07916', '-0.251', '-0.07684', '-0.0665', '-0.2383', '-0.1519', '-0.241', '0.5044', '0.647', '-0.1788', '0.2434', '0.1401', '0.01546', '-0.5747', '-0.2225', '0.7793', '0.03217', '0.1523', '0.2083', '-0.1664', '-0.2085', '-0.702', '0.0908', '0.1732', '-0.406', '-0.598', '-0.9795', '-0.3894', '0.6455', '0.313', '-0.2886', '-0.3748', '0.2048', '0.3555', '-0.204', '0.0759', '-0.3115', '-0.5874', '-0.6997', '0.2573', '-0.815', '0.528', '-0.1771', '-0.142', '-0.4639', '0.303', '-0.0575', '0.2737', '0.3164', '-0.5347', '0.2268', '0.3254', '0.7114', '-0.3662', '0.392', '-0.1711', '-0.3914', '0.4333', '0.2964', '0.928', '0.0966', '-0.4512', '0.03616', '-0.4749', '-0.08276', '0.091', '0.5005', '0.8584', '0.6753', '0.2354', '0.0722', '-0.3325', '0.4336', '0.0706', '-0.5513', '0.5815', '-0.2927', '0.3274', '0.2225', '0.823', '-0.02782', '0.6855', '-0.175', '-0.3845', '-0.5547']",C84675,,,,,,
mondo:0018950,3-methylcrotonyl-CoA carboxylase deficiency,"['3-MCC deficiency', '3MCC deficiency', 'Methylcrotonyl-CoA carboxylase deficiency', 'methylcrotonylglycinuria', 'BMCC deficiency', '3-methylcrotonylglycinuria', 'MCC deficiency', 'MCCD']",0050710,,6,CN239165,"['0.2467', '0.02377', '-0.7417', '0.002596', '-0.08673', '-0.2903', '0.3977', '0.807', '-0.2598', '0.251', '0.0456', '-0.3997', '0.523', '0.2524', '-0.1604', '0.2854', '-0.402', '-0.4666', '-0.6353', '-0.772', '-0.07855', '-0.816', '0.5747', '0.09143', '-0.0885', '-0.536', '-0.2343', '-0.03214', '0.046', '-0.3865', '0.4216', '0.136', '0.656', '0.479', '-0.852', '0.2983', '-0.563', '-0.1306', '0.1973', '0.0938', '-0.04373', '-0.2083', '0.722', '-0.1788', '-0.1212', '-0.259', '-0.0535', '-0.4363', '0.01921', '0.5728', '-0.451', '-0.4666', '-0.6113', '-0.3447', '0.2888', '-0.1219', '0.1711', '-0.3914', '-0.36', '0.457', '0.1687', '-0.2827', '0.7036', '-0.3564', '-0.7617', '0.4333', '0.5825', '0.3665', '-0.09753', '0.2294', '-0.3518', '0.2205', '-0.525', '0.777', '0.4163', '0.1414', '0.3347', '-0.02412', '0.2988', '-0.2041', '0.203', '-0.1285', '-0.3892', '0.1216', '0.3708', '1.036', '-0.1853', '-0.1265', '0.7764', '-0.2551', '0.04666', '0.3022', '-0.3257', '-0.2886', '0.279', '0.8003', '-0.2106', '-0.5796', '-0.1376', '-0.01868']",C98674,,,,,,
mondo:0018951,distal myopathy with vocal cord weakness,"['MATR3-related distal myopathy', 'distal myopathy 2', 'vocal cord and pharyngeal distal myopathy', 'MPD2', 'VCPDM']",,,600,CN205357,,,,,,,,
mondo:0018952,argyria,['Silver staining'],,,60014,,,,,D001129,,,10003094,
mondo:0018953,parietal foramina,"['Caitlin marks', 'hereditary cranium bifidum', 'fenestrae parietales symmetricae', 'enlarged parietal foramina', 'catlin marks', 'foramina parietalia permagna', 'symmetric parietal foramina']",0060285,,60015,,"['-0.6094', '-0.3694', '0.2349', '-0.5938', '0.531', '-0.002764', '0.474', '0.661', '-0.43', '-0.4075', '-0.1965', '-0.4058', '0.2291', '-0.1693', '-0.1558', '0.1947', '-0.3657', '-0.559', '-0.1544', '-0.552', '0.1987', '0.07935', '0.3599', '-0.362', '0.1527', '-0.02852', '0.1167', '0.10724', '0.501', '0.2683', '-0.3396', '-0.2107', '0.267', '0.1709', '0.00783', '-0.04367', '0.311', '0.285', '-0.1357', '-0.04514', '1.247', '-0.1404', '0.6616', '-0.411', '0.276', '0.02415', '-0.0862', '-0.02696', '0.2487', '0.33', '0.5586', '-0.12274', '0.10126', '-0.6416', '-0.1255', '-0.1437', '0.1783', '0.495', '-0.3748', '0.5195', '-0.245', '0.05783', '-0.0885', '-0.543', '0.0356', '0.6973', '0.688', '0.5845', '-0.2524', '0.405', '0.29', '0.4817', '0.1956', '0.12494', '0.0294', '0.1654', '-0.1879', '-0.1292', '0.092', '-0.1426', '-0.1696', '0.11975', '-0.0551', '0.1289', '-0.2054', '0.637', '0.1528', '0.2189', '-0.2089', '-0.0746', '-0.963', '0.2329', '-0.4792', '-0.0331', '1.057', '-0.2056', '0.6895', '-0.6475', '0.5244', '0.1077']",,,C566826,,,,0002697
mondo:0018954,Loeys-Dietz syndrome,"['aortic aneurysm syndrome, Loeys-Dietz type', 'aortic aneurysm syndrome due to TGF-beta receptors anomalies']",0050466,,60030,C2697932,"['0.03552', '0.1533', '0.2489', '-0.2507', '0.3108', '-0.2045', '-0.1244', '-0.05862', '-0.1661', '-0.05438', '-0.157', '-0.306', '0.3906', '0.0387', '-0.005363', '0.05807', '-0.0767', '-0.09875', '-0.05316', '-0.1815', '0.1842', '-0.1214', '0.6953', '-0.1675', '0.1481', '0.5005', '0.3237', '-0.1797', '0.69', '-0.1863', '0.357', '0.1471', '0.634', '0.326', '0.10645', '-0.4414', '0.1387', '-0.0482', '-0.1719', '-0.8643', '0.1301', '-0.2493', '0.00781', '-0.1715', '0.2382', '-0.4224', '0.2382', '0.3484', '0.0682', '-0.1465', '-0.11163', '-0.273', '-0.0792', '-0.0734', '-0.2251', '-0.4275', '0.00886', '-0.03087', '-0.1577', '0.1313', '0.2615', '-0.2277', '-0.1321', '-0.05515', '-0.1555', '-0.0975', '0.135', '0.1628', '-0.452', '0.4065', '-0.589', '-0.3171', '0.1427', '-0.003174', '-0.0838', '0.0755', '-0.02052', '0.0739', '-0.11444', '-0.346', '0.1206', '-0.02158', '-0.3037', '0.4373', '-0.1459', '0.1104', '0.2666', '0.3433', '0.0757', '0.06073', '-0.09796', '0.3726', '0.1849', '0.2186', '0.751', '-0.00936', '0.5845', '-0.002905', '0.1163', '0.1658']",C75006,,D055947,759.89,,,
mondo:0018955,recurrent respiratory papillomatosis,"['RRP', 'juvenile laryngeal papilloma', 'laryngeal papilloma, recurrent', 'respiratory papillomatosis, recurrent', 'AORRP (type)', 'recurrent respiratory papillomatosis', 'juvenile-onset recurrent respiratory papillomatosis (type)', 'JORRP (type)', 'adult-onset recurrent respiratory papillomatosis (type)']",,,60032,C1168198,,C128637,,C535297,078.19,,10059314,
mondo:0018956,idiopathic bronchiectasis,,,,60033,C0339985,,,,,,,,
mondo:0018957,pudendal neuralgia,"['pudendal algia', 'pudendal neuralgia by pudendal nerve entrapment', 'pudendal nerve neuralgia', 'neuralgia of pudendal nerve', 'Alcock syndrome', 'Pudendalgia', 'pudendal nerve entrapment syndrome']",,,60039,CN226268,,,,D060545,729.2,,,
mondo:0018958,nemaline myopathy,"['Rod-body myopathy', 'rod myopathy', 'nemaline rod myopathy', 'nemaline body disease', 'Rod body disease', 'congenital rod disease', 'NEM', 'nemaline rod disease', 'NM']",3191,,607,C0206157,"['0.245', '0.2935', '-0.4634', '-0.01423', '0.1409', '-0.1517', '-0.1403', '1.243', '-0.9214', '-0.3354', '-0.3118', '-0.4143', '-0.1823', '-0.1672', '0.6694', '0.1833', '-0.561', '-0.2448', '0.07104', '-0.6675', '0.1161', '-0.04938', '0.5483', '0.2473', '-0.163', '0.2656', '-0.3367', '0.02528', '0.03607', '-0.2378', '0.3323', '0.5796', '-0.02454', '0.003223', '-0.3406', '-0.4143', '-0.3208', '-0.06586', '0.09796', '-0.574', '-0.2683', '-0.4336', '-0.29', '-0.1096', '0.4475', '0.6313', '-0.1501', '0.269', '0.2517', '0.5146', '-0.358', '-0.2144', '-0.185', '-0.4934', '-0.2308', '-0.4753', '0.253', '0.03165', '-0.0672', '0.06464', '0.055', '-0.184', '-0.2168', '-0.05164', '-0.0887', '-0.3528', '0.603', '0.487', '-0.9907', '0.1483', '0.777', '-0.3289', '-0.1183', '0.1978', '0.622', '-0.003727', '0.02597', '-0.1332', '-0.6416', '-0.3945', '0.1572', '-0.4094', '0.3904', '0.1625', '-0.10443', '0.759', '-0.5083', '0.02946', '0.5625', '-0.286', '0.3223', '0.3638', '-0.04196', '0.6826', '0.1733', '0.03427', '0.1841', '0.2405', '-0.266', '-0.0453']",,,D017696,,,,
mondo:0018959,potassium-aggravated myotonia,"['Myotonia Congenita, Acetazolamide-Responsive', 'PAM', 'Myotonia Fluctuans', 'Laryngospasm, Severe Neonatal Episodic', 'Sodium Channel Muscle Disease', 'Myotonia Permanens', 'K+-aggravated myotonia', 'MYOTONIA, POTASSIUM-AGGRAVATED', 'Myotonia Congenita, Atypical', 'K-aggravated myotonia', 'myotonia congenita, atypical, acetazolamide-responsive', 'Potassium aggravated myotonia']",,608390,612,C2931826,"['-0.5615', '-0.02017', '-0.2979', '-0.3257', '-0.3516', '-0.4739', '0.6367', '0.327', '-0.7437', '-0.512', '-0.423', '0.3157', '-0.02115', '0.479', '0.2311', '0.471', '-0.2417', '-0.5166', '-0.2273', '-0.775', '-0.1322', '0.1776', '0.3518', '0.4846', '-0.2822', '0.457', '0.09656', '-0.2343', '-0.10803', '-0.1527', '-0.1925', '0.266', '0.4575', '0.316', '-0.4683', '0.07904', '-0.512', '-0.0914', '0.1198', '-0.3489', '0.2064', '-0.5586', '0.749', '0.298', '0.507', '-0.2832', '-0.4722', '0.3994', '0.7085', '0.859', '-0.4255', '-0.594', '0.9863', '-0.038', '0.407', '-0.0113', '0.6196', '0.04044', '0.2446', '0.1819', '-0.02884', '0.2537', '-0.1831', '0.0281', '-0.1169', '0.2805', '0.1241', '0.1798', '-0.099', '0.187', '-0.4058', '-0.3706', '0.4634', '0.1522', '1.109', '0.91', '0.2418', '-0.231', '0.2329', '0.1602', '0.2316', '-0.02522', '-0.2454', '0.2164', '0.1797', '0.3706', '0.2673', '0.297', '0.856', '0.02051', '0.0981', '-1.058', '0.0713', '0.2322', '0.3413', '0.1764', '0.5293', '-0.737', '-0.4873', '-0.478']",C122788,,C538353,,,,
mondo:0018960,congenital primary megaureter,"['congenital megalo-ureter', 'CGM', 'congenital primary megalo-ureter', 'congenital giant megaureter']",,,617,,,,,,,,,
mondo:0018961,familial melanoma,['hereditary melanoma (disease)'],6846,,618,C2314896,"['0.6265', '-0.1555', '-1.036', '0.2227', '0.6167', '0.2727', '-0.1206', '0.555', '-0.5693', '-0.0645', '0.9355', '0.1581', '-0.517', '0.454', '-0.7563', '-0.2666', '0.2917', '-0.5605', '0.08203', '-0.1025', '-0.2158', '0.4263', '-0.1603', '-0.386', '0.2358', '-0.5737', '-0.629', '-0.2986', '0.2263', '0.05927', '0.958', '-0.6465', '0.1514', '-0.5938', '0.1589', '0.67', '-0.304', '-0.1714', '0.09106', '-0.2737', '0.45', '-0.9004', '0.02219', '-0.1334', '0.05655', '-0.5864', '-0.102', '-0.37', '-0.2607', '-0.67', '0.1418', '-0.2651', '0.304', '-0.721', '-0.758', '-0.3606', '-0.2294', '-0.225', '-0.822', '-0.6987', '-0.0852', '-0.0879', '-0.754', '0.5957', '0.05093', '1.201', '0.684', '0.4448', '0.2395', '0.8574', '0.1589', '0.4111', '0.2098', '0.282', '0.5728', '0.1865', '-0.8784', '0.6177', '-0.0931', '-0.2917', '0.1137', '-0.2084', '0.2744', '-0.1456', '-0.1439', '-0.7695', '-0.007603', '0.2961', '0.8774', '0.04715', '0.8315', '0.08563', '-0.4775', '0.4666', '0.7974', '0.507', '-0.3652', '-0.8276', '-0.8975', '0.539']",C8498,,,,,,
mondo:0018962,common mesentery,['universal mesentery'],,,620,C0266235,,,,,,,,
mondo:0018963,hereditary methemoglobinemia,"['autosomal recessive methemoglobinemia', 'congenital methemoglobinemia', 'hereditary methemoglobinemia']",,,621,C0272087,"['-0.731', '-0.341', '-0.1906', '0.03003', '0.3127', '-0.4104', '-0.3396', '-0.0361', '-0.3286', '-0.295', '-0.4004', '0.114', '0.259', '0.1724', '-0.3982', '0.3013', '-0.09814', '-0.463', '-0.001737', '-0.6475', '0.05453', '-0.2666', '0.928', '-0.31', '0.10834', '0.2273', '0.438', '0.1244', '-0.2686', '0.0995', '0.5435', '0.10345', '0.2361', '0.429', '-0.8604', '-0.544', '0.2317', '-0.168', '0.0846', '0.4673', '0.5273', '-0.3655', '0.4307', '-0.03156', '0.1453', '-0.07', '-0.0042', '0.11255', '-0.2603', '-0.4688', '0.10675', '-0.535', '0.0316', '0.1985', '0.2189', '0.245', '0.6094', '0.1206', '-0.619', '0.429', '-0.8506', '0.09265', '0.459', '-0.2386', '-0.2418', '-0.4937', '0.3044', '-0.02039', '-0.272', '0.5747', '-0.2379', '-0.0595', '0.325', '-0.06088', '0.555', '0.757', '-0.0317', '-0.1941', '-0.2966', '0.217', '0.6084', '-0.4028', '0.04132', '-0.01744', '-0.0915', '-0.02652', '0.272', '0.262', '0.226', '0.437', '-0.04254', '0.1412', '0.3748', '-0.2532', '0.8013', '0.7275', '-0.3757', '-0.3997', '0.2018', '-0.4023']",C98898,,C580280,,,,
mondo:0018964,homocystinuria without methylmalonic aciduria,"['methylcobalamin deficiency', 'functional methionine synthase deficiency']",,,622,C4303479,,,,,,,,
mondo:0018965,Alport syndrome,"['hereditary nephritis', 'Alport^s syndrome', 'Alport deafness-nephropathy']",10983,,63,C1567741,"['0.4204', '-0.02698', '-0.1942', '-0.1306', '0.3896', '-0.4138', '0.02133', '0.777', '-0.7827', '0.00947', '0.4846', '-0.1506', '-0.395', '0.585', '-0.4504', '-0.2842', '-0.2808', '-0.684', '0.5947', '-0.2192', '-0.00596', '-0.1705', '0.7764', '0.000315', '0.1328', '-0.3457', '-0.3687', '0.0958', '0.01662', '0.4414', '0.672', '-0.3254', '0.4976', '-0.2133', '0.11334', '-0.4448', '-0.4885', '-0.2174', '-0.163', '-0.2462', '-0.1798', '0.4226', '0.663', '0.194', '0.1417', '-0.364', '-0.6772', '-0.4622', '0.276', '-0.08215', '0.4583', '-0.385', '0.076', '-0.9556', '0.637', '-0.465', '0.9087', '-0.3203', '-0.6616', '0.05795', '0.0975', '0.2651', '0.1649', '0.4534', '0.09', '-0.2727', '0.331', '0.2422', '-0.08105', '0.1545', '-0.2119', '-0.4663', '0.1677', '0.7134', '0.762', '-0.2751', '0.3008', '-0.1114', '-0.1464', '0.0596', '-0.408', '0.3157', '0.321', '0.3247', '-0.3', '0.1914', '0.5938', '-0.1348', '-0.12054', '0.5776', '0.3303', '0.4', '0.07874', '0.1958', '0.7383', '-0.347', '0.496', '-0.7227', '-0.1841', '0.4111']",C34842,,D009394,,Q87.81,10001843,
mondo:0018967,short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia,,,,632,,"['-0.3674', '0.2742', '0.1127', '-0.1738', '0.1984', '0.0421', '0.05676', '0.2128', '-0.1083', '-0.1752', '-0.00997', '-0.03616', '-0.003767', '0.1067', '0.004177', '-0.0737', '0.0879', '0.08704', '-0.383', '-0.3855', '-0.08844', '-0.0713', '0.218', '-0.2274', '0.1137', '-0.05286', '0.006714', '-0.1748', '-0.05164', '-0.2319', '0.1871', '-0.01108', '0.1802', '0.06235', '-0.03897', '-0.02403', '0.00945', '-0.06097', '-0.1743', '-0.1322', '0.08936', '-0.0893', '0.02971', '-0.0976', '0.01883', '-0.2225', '0.11597', '0.012695', '0.02194', '0.03967', '0.02808', '-0.1857', '0.0296', '0.1126', '-0.2103', '0.04727', '0.1658', '-0.3481', '-0.1853', '0.1382', '0.11804', '0.1027', '-0.075', '-0.01334', '-0.02832', '0.003408', '0.162', '0.1787', '-0.2908', '0.06586', '-0.1505', '0.1469', '0.1399', '-0.217', '0.10846', '0.08636', '0.07404', '-0.02466', '-0.0716', '-0.01703', '0.01421', '0.0826', '-0.0873', '0.04617', '0.0008173', '0.1265', '0.2126', '-0.01625', '0.3843', '0.07544', '0.09595', '0.1812', '-0.1042', '-0.1614', '0.4663', '0.07434', '0.0748', '-0.2405', '-0.006702', '0.2108']",,,,,,,
mondo:0018968,iniencephaly,,,,63259,C0152234,,C124549,,,740.2,Q00.2,10022034,
mondo:0018969,craniorachischisis,"['cranial rachischisis', 'craniorachischisis', 'craniorachischisis (disease)']",,,63260,C0152426,,C98907,,,740.1,,10011321,0030770
mondo:0018971,isolated oxycephaly,"['pyrgocephaly', 'hypsicephaly', 'acrocephaly', 'hypsocephaly', 'turricephaly']",,,63440,,"['0.1478', '-0.4395', '-0.5273', '0.252', '0.2778', '0.1449', '0.4402', '0.972', '-0.798', '-0.2454', '-0.3794', '0.09644', '0.4985', '0.3806', '-0.0996', '-0.1158', '0.2737', '-0.2922', '0.11926', '-0.916', '0.2712', '-0.05032', '0.789', '-0.4844', '0.5977', '0.701', '-0.4043', '-0.2852', '0.051', '0.444', '-0.01386', '0.1255', '0.2615', '-0.1362', '-0.4688', '0.1566', '-0.04404', '-0.8467', '-0.0349', '-0.37', '0.4097', '0.1354', '0.5376', '-0.3005', '0.8496', '0.09454', '-0.11224', '-0.06464', '-0.15', '-0.5107', '0.1832', '-0.1846', '-0.324', '-0.279', '-0.3696', '0.5776', '0.074', '-0.3958', '-0.2246', '0.1748', '-0.03766', '-0.0756', '0.256', '0.286', '-0.568', '-0.2281', '0.1388', '0.429', '-0.3005', '0.2206', '-0.0777', '0.9624', '0.2864', '-0.52', '-0.1854', '0.1455', '0.0965', '-0.0791', '-0.1721', '-0.8867', '-0.229', '0.276', '-0.625', '0.433', '0.3801', '0.2705', '0.4353', '0.1635', '0.2335', '-0.2432', '-0.1727', '0.6807', '-0.136', '0.1026', '0.872', '0.1853', '0.371', '-0.2006', '0.8896', '-0.2954']",,,,,,,
mondo:0018973,patterned dystrophy of the retinal pigment epithelium,,,,63454,C1868569,"['-0.1372', '0.0352', '0.003386', '-0.01349', '0.1913', '-0.2296', '-0.07715', '0.0732', '-0.1372', '-0.10297', '-0.03275', '-0.11127', '-0.1783', '-0.04553', '-0.0817', '-0.1742', '0.0748', '-0.0505', '0.005035', '-0.3108', '-0.09705', '-0.1116', '0.03503', '0.1401', '-0.03876', '-0.01785', '-0.05774', '-0.1108', '-0.0246', '0.06415', '0.1956', '-0.01723', '0.1068', '-0.00158', '0.03032', '0.1216', '-0.00637', '-0.0955', '0.0352', '-0.2734', '0.11285', '-0.2573', '0.0725', '-0.05005', '-0.1385', '0.01588', '-0.03262', '0.0742', '0.1011', '0.07056', '0.1285', '0.013664', '0.0851', '-0.0935', '-0.03796', '-0.2142', '0.2866', '-0.002909', '-0.3228', '-0.098', '0.1863', '-0.02184', '0.0797', '0.1417', '0.03845', '-0.05405', '0.3003', '0.2194', '-0.205', '0.189', '-0.1935', '-0.1098', '0.06635', '-0.05344', '0.1844', '0.01738', '0.005035', '-0.05707', '-0.0755', '-0.10785', '0.03091', '-0.02011', '-0.06052', '0.2146', '-0.13', '-0.08154', '0.01749', '0.1721', '0.187', '0.0618', '0.04736', '0.1738', '0.1123', '0.1573', '0.3235', '0.0436', '0.168', '-0.1879', '-0.1032', '0.1414']",,,C536309,,H35.5,,
mondo:0018974,paraneoplastic pemphigus,,0080852,,63455,C1112570,,,0008602,,,L10.81,10057056,
mondo:0018975,neurofibromatosis type 1,"['NF1', 'neurofibromatosis type 1 microdeletion syndrome', 'neurofibromatosis', 'von Reklinghausen disease', 'peripheral neurofibromatosis', 'neurofibromatosis type 1', 'Recklinghausen^s disease', 'Von Recklinghausen disease', 'neurofibromatosis, type I', 'neurofibromatosis 1', 'neurofibromatosis, peripheral type', 'neurofibromatosis, type 1', 'Nf1-Microdeletion syndrome', 'type 1 neurofibromatosis']",0111253,162200,636,C0027831,"['0.497', '0.616', '0.3523', '-0.577', '0.7505', '-0.09735', '-0.1548', '0.773', '-0.859', '-0.3545', '0.011566', '0.09576', '0.2019', '0.533', '-0.2612', '0.02032', '0.1197', '0.1553', '-0.5195', '0.0544', '-0.3345', '-0.3286', '0.2173', '0.3223', '-0.2751', '-0.4636', '-0.2742', '-0.62', '0.4143', '0.274', '0.884', '-0.876', '0.471', '-0.181', '-0.373', '-0.1407', '-0.542', '0.2308', '0.2194', '0.02716', '0.4287', '0.2485', '0.09766', '-0.345', '0.6016', '0.1904', '-0.1428', '0.06976', '0.9277', '-0.1605', '0.1453', '0.269', '0.1078', '-0.06335', '0.4336', '0.3337', '-0.3306', '0.2896', '-0.2551', '-0.1696', '-0.628', '-0.1785', '-0.4148', '-0.2798', '-0.01536', '0.6694', '0.3528', '0.802', '-0.4058', '0.6724', '0.536', '0.2489', '-0.144', '-0.8887', '0.693', '-0.2039', '-0.142', '0.7734', '0.1443', '-0.242', '-0.1399', '0.02908', '0.519', '0.2192', '-0.7383', '-0.748', '0.6157', '0.4087', '0.4893', '0.4556', '-0.573', '0.36', '-0.672', '-0.7197', '0.6904', '-0.0889', '0.8413', '-0.03995', '0.563', '0.525']",C3273,,D009456,237.71,,10047712,
mondo:0018976,schisis association,['Midline development field defects'],,,63862,C2931271,,,,C536633,,,,
mondo:0018977,polyneuropathy associated with IgM monoclonal gammapathy with anti-MAG,"['anti-MAG neuropathy', 'neuropathy associated with monoclonal IgM antibodies to myelin-associated glycoprotein']",,,639,C1736154,,,,,,,,
mondo:0018978,IgG4-related mediastinitis,"['sclerosing mediastinitis', 'fibrosing mediastinitis', 'idiopathic mediastinal fibrosis', 'mediastinal fibrosis']",,,63999,,,,,C536136,,,10027074,
mondo:0018979,multifocal motor neuropathy,"['multifocal motor neuropathy with conduction block', 'MMNCB', 'MMN']",,,641,C0393847,,,,,357.89,G61.82,,
mondo:0018980,"acrofacial dysostosis, Kennedy-Teebi type",['Kennedy-Teebi syndrome'],,,64542,CN205418,,,,,,,,
mondo:0018981,benign idiopathic neonatal seizures,"['benign nonfamilial neonatal seizures', 'BINS']",,,64545,CN205419,,,,,,,,
mondo:0018982,Niemann-Pick disease type C,['NPC'],,,646,,"['0.4524', '0.959', '-0.4075', '0.1693', '-0.1738', '-1.09', '-0.4246', '0.2463', '-0.3267', '-0.2079', '-0.4255', '-0.65', '0.2642', '0.746', '0.2041', '-0.3423', '-0.1005', '-0.5205', '-0.6772', '-0.3867', '-0.05096', '-0.7593', '0.595', '0.2009', '0.2065', '0.007446', '0.167', '-0.0877', '-0.3086', '0.2083', '0.722', '0.08496', '0.2947', '-0.591', '-0.38', '0.08154', '-0.668', '0.3018', '-0.2595', '-0.2693', '0.1921', '-0.1953', '0.037', '0.2097', '-0.6343', '-0.1367', '-0.1937', '-0.3296', '0.07275', '0.4126', '-0.08624', '0.2302', '-0.06116', '-0.2042', '-0.02629', '-0.5825', '-0.3506', '0.3005', '-0.2607', '-0.3818', '-0.02441', '0.10596', '0.7866', '-0.285', '-0.5684', '-0.0729', '0.636', '-0.2258', '-0.4343', '0.01913', '-0.5894', '-0.1757', '-0.3325', '0.3909', '0.3586', '-0.2278', '0.3865', '0.2069', '0.3909', '0.2', '-0.2057', '-1.061', '-0.297', '0.0158', '0.02106', '-0.05936', '0.617', '-0.1514', '1.352', '-0.1478', '0.000682', '0.3477', '-0.167', '-0.0791', '0.00631', '0.6167', '-0.324', '-0.2979', '0.4084', '-0.0764']",,,D052556,,,,
mondo:0018983,Tolosa-Hunt syndrome,"['painful ophthalmoplegia', 'THS', 'nonspecific inflammation of the cavernous sinus or superior orbital fissure', 'Tolosa-Hunt syndrome', 'Tolosa Hunt syndrome']",1278,,64686,CN205421,,C85193,,D020333,,,10051526,
mondo:0018984,Oroya fever,"['bartonellosis due to Bartonella bacilliformis infection', 'Carrion^s disease', 'Carrión disease', 'Bartonella bacilliformis caused disease or disorder', 'Oroya fever', 'Carrion disease']",0050398,,64692,CN205422,,C128441,,,,,,
mondo:0018987,granulomatous mastitis,"['idiopathic granulomatous mastitis', 'granulomatous lobular mastitis', 'idiopathic granulomatous lobular mastitis']",,,64722,C0405469,,,,D058890,,,,
mondo:0018988,iridocorneal endothelial syndrome,['ICE syndrome'],,,64734,CN205427,,C84792,,D057129,,,10053678,
mondo:0018989,recurrent acute pancreatitis,,,,64740,C0267937,,C184324,,,,,10033657,
mondo:0018991,hepatoportal sclerosis,['obliterative portal venopathy'],,,64743,C4273756,,,,,,,,
mondo:0018992,IgG4-related thyroid disease,"['Riedel disease', 'Riedel thyroiditis', 'Riedel fibrosing thyroiditis', 'Riedel^s fibrosing thyroiditis']",14351,,64744,C1335787,,C35827,,,,,10039142,
mondo:0018993,Charcot-Marie-Tooth disease type 2,"['Charcot-Marie-Tooth type 2', 'CMT2', 'hereditary motor and sensory neuropathy type 2', 'autosomal dominant Charcot-Marie-Tooth disease type 2', 'hereditary motor and sensory neuropathy Guadalajara neuronal type', 'autosomal dominant axonal Charcot-Marie-Tooth disease', 'hereditary motor and sensory neuropathy Okinawa type']",0050539,,64746,,"['0.2566', '0.1543', '0.02257', '0.1517', '-0.246', '-0.2212', '-0.3057', '0.4297', '-0.6543', '-0.1833', '-0.03735', '0.2944', '-0.4915', '0.2391', '-0.1853', '-0.258', '-0.3572', '-0.6543', '-0.142', '-0.4543', '0.02324', '0.2947', '0.508', '0.4607', '0.576', '0.4304', '-0.00771', '0.2754', '-0.02995', '0.013596', '0.2379', '-0.713', '-0.05963', '-0.003347', '0.357', '-0.6323', '-0.1366', '-0.0523', '0.493', '-0.369', '-1.514', '-0.1615', '-0.3008', '0.4756', '-0.05753', '-0.4585', '0.1759', '-0.003975', '-0.2717', '0.006126', '0.10803', '0.2015', '-0.2825', '-0.963', '0.413', '-0.1492', '0.2311', '0.4377', '-0.738', '-0.03842', '-0.3254', '0.0916', '0.6025', '0.812', '-0.712', '0.9307', '0.2515', '0.649', '-0.6235', '0.4526', '-0.5586', '0.0873', '0.4714', '-0.3022', '0.9995', '0.64', '-0.5474', '0.4583', '0.001933', '-0.3723', '-0.02791', '0.2172', '0.572', '0.4277', '0.06793', '-0.0795', '0.206', '0.4072', '0.759', '0.16', '-0.1109', '-0.03717', '0.291', '0.2489', '0.655', '0.725', '0.543', '-0.806', '-0.274', '0.4817']",,,,356.0,,,
mondo:0018994,Charcot-Marie-Tooth disease type X,"['X-linked hereditary motor and sensory neuropathy', 'COWCK', 'X-linked Charcot-Marie-Tooth disease', 'CMTX']",0050542,,64747,CN205436,,,,,356.9,,,
mondo:0018995,Charcot-Marie-Tooth disease type 4,"['CMT4', 'autosomal recessive demyelinating Charcot-Marie-Tooth', 'AR-CMT1']",0050541,,64749,CN043578,,,,,,,,
mondo:0018996,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 2","['AOA2', 'spinocerebellar ataxia, autosomal recessive type 1', 'ataxia-oculomotor apraxia 2', 'ataxia with oculomotor apraxia type 2', 'autosomal recessive spinocerebellar ataxia-1', 'spinocerebellar ataxia, autosomal recessive 1', 'SCAR1', 'ataxia-ocular apraxia 2', 'SCAN 2', 'SCAN2', 'spinocerebellar ataxia with axonal neuropathy type 2', 'ataxia-oculomotor apraxia type 2']",0050755,606002,64753,CN205441,"['0.05576', '0.01499', '-0.1267', '0.06235', '-0.061', '-0.622', '0.2534', '0.413', '-0.754', '-0.647', '0.0769', '0.3389', '-0.0722', '0.2876', '0.439', '-0.4307', '-0.2864', '-0.3342', '0.2441', '-0.7207', '-0.094', '-0.336', '0.01816', '-0.3647', '0.2429', '-0.4902', '-0.2827', '-0.02182', '-0.03116', '-0.7656', '0.0841', '0.547', '-0.4133', '-0.2322', '0.147', '0.09515', '-0.1233', '0.2045', '0.4976', '0.3374', '0.2559', '0.116', '-0.3064', '0.362', '0.4517', '-0.7026', '0.2286', '0.305', '0.272', '-0.1415', '-0.2705', '0.1323', '-0.11554', '-0.563', '0.03757', '-0.6074', '0.4648', '0.4514', '-0.282', '0.4048', '-0.392', '0.3508', '0.2487', '-0.2113', '-0.444', '0.4153', '0.2094', '0.416', '-0.4011', '0.3042', '0.7974', '0.4192', '-0.2319', '-0.6445', '0.9023', '0.3071', '0.1159', '0.1045', '0.002174', '0.5703', '-0.3386', '-0.9873', '0.3313', '0.556', '-0.1771', '-0.688', '0.147', '0.01252', '0.5957', '0.444', '0.411', '0.2754', '0.01901', '-0.298', '0.8965', '0.871', '0.4617', '0.404', '-0.1556', '0.02055']",C165500,,C537308,,,,
mondo:0018997,Noonan syndrome,"['Noonan syndrome', 'Turner^s phenotype, karyotype normal', 'Ullrich-Noonan syndrome', 'Noonan-Ehmke syndrome', 'Noonan^s syndrome', 'pseudo-Ullrich-Turner syndrome']",3490,,648,C0028326,"['0.2776', '0.1619', '0.5205', '-0.3975', '-0.145', '-0.10315', '0.3706', '0.999', '-0.63', '-0.5293', '0.546', '-0.12335', '0.2205', '0.3599', '-0.2969', '-0.04633', '-0.337', '0.08545', '-0.7812', '-0.1086', '-0.2097', '-0.00139', '-0.0661', '-0.526', '0.2568', '-0.2708', '-0.4294', '0.31', '1.132', '0.3877', '0.4702', '-0.557', '0.3896', '0.6953', '-0.41', '-0.328', '-0.2325', '0.6504', '0.3828', '-0.4084', '0.4956', '0.8853', '0.0623', '0.1888', '0.06323', '-0.1351', '-0.009796', '0.2656', '0.4902', '-0.11475', '-0.3794', '0.1494', '-0.2494', '0.3306', '-0.4023', '-0.2769', '-0.02818', '0.2393', '-0.07733', '-0.2974', '0.2007', '-0.3486', '0.6777', '-0.08356', '0.489', '-0.1014', '0.04013', '0.3025', '0.03705', '0.838', '0.2537', '0.276', '-0.1716', '-0.097', '0.4373', '0.06433', '0.3652', '0.11096', '0.087', '-0.4944', '0.3281', '-0.3337', '-0.12225', '-0.0944', '-0.03038', '-0.3933', '0.3174', '-0.2124', '0.9575', '0.669', '-0.05206', '0.1656', '-0.135', '-0.3884', '0.6914', '-0.1879', '0.4932', '-0.362', '0.07465', '0.2056']",C34854,,D009634,759.89,,10029748,
mondo:0018998,Leber congenital amaurosis,"['congenital retinal blindness', 'congenital absence of the rods and cones', 'Leber^s congenital amaurosis', 'Leber^s disease', 'Leber^s congenital tapetoretinal degeneration', 'LCA', 'Leber^s congenital tapetoretinal dysplasia', 'amaurosis congenita of Leber', 'Leber^s amaurosis']",14791,,65,C0339527,"['-0.1995', '-0.322', '0.1447', '0.2651', '-0.01869', '-0.0812', '0.2834', '0.557', '-0.1753', '-0.4934', '0.06683', '-0.42', '-0.004814', '-0.03253', '0.252', '-0.02354', '0.3806', '-0.03412', '0.1669', '-1.1045', '-0.3071', '0.007446', '0.0408', '0.2097', '-0.1255', '0.1671', '-0.2898', '0.74', '-0.392', '0.2303', '0.7856', '0.2343', '0.10535', '0.2485', '-0.1459', '0.3816', '-0.362', '-0.012436', '-0.10767', '-0.4412', '0.3489', '-0.05197', '-0.08276', '0.03885', '-0.267', '0.0798', '0.1624', '-0.1283', '0.1702', '0.5166', '-0.5576', '-0.3699', '-0.0767', '-1.006', '0.6016', '0.2607', '0.989', '0.0638', '-0.4333', '0.3472', '0.1909', '0.1469', '-0.0387', '0.9624', '-0.528', '-0.0638', '0.458', '0.03903', '-0.1799', '0.2217', '-0.1978', '0.298', '-0.1847', '-0.2812', '1.205', '-0.6323', '0.662', '-0.668', '-0.7773', '0.2192', '0.0729', '-0.2119', '-0.341', '0.912', '-0.1494', '-0.329', '0.04083', '0.7017', '0.05087', '0.342', '0.2622', '0.1696', '-0.2915', '0.03705', '0.232', '-0.06216', '0.67', '-0.3633', '0.1289', '0.2761']",C129075,,D057130,,H35.5,10070667,
mondo:0018999,LCAT deficiency,['lecithin-cholesterol acyltransferase deficiency'],,,650,,"['-0.378', '0.2017', '-0.04782', '0.1407', '0.4062', '-0.6807', '-0.7764', '0.767', '0.2717', '-0.65', '-0.077', '-0.22', '-0.2112', '-0.3027', '-0.3374', '-0.5547', '0.3013', '-0.2622', '-0.0153', '-0.312', '0.1808', '-0.2301', '0.683', '0.0852', '0.09595', '0.3062', '-0.03998', '0.227', '0.0995', '-0.2886', '0.3398', '-0.07324', '0.4653', '0.2983', '-0.1127', '-0.3174', '-0.09436', '-0.6123', '0.02208', '-0.06885', '0.04333', '-0.2216', '0.555', '-0.328', '-0.3545', '0.1809', '0.2632', '0.1669', '0.2537', '-0.0883', '0.652', '-0.01467', '0.1492', '0.003368', '-0.2627', '-0.2744', '0.3855', '-0.2377', '-0.649', '0.1063', '0.0667', '-0.2489', '0.2773', '-0.5312', '0.3276', '-0.365', '0.3904', '0.754', '-0.2125', '-0.0782', '0.07495', '-0.64', '-0.2216', '0.3738', '0.4062', '0.507', '0.3005', '0.0734', '-0.2778', '0.1233', '0.113', '-0.1768', '-0.1243', '0.0679', '0.4736', '-0.02383', '0.1766', '-0.1959', '0.5986', '-0.1288', '0.5396', '0.3735', '0.2947', '-0.2512', '0.8066', '0.637', '0.2908', '-0.5723', '-0.2213', '-0.001395']",,,,,,,
mondo:0019000,perineural cyst,"['sacral Tarlov cysts', 'Tarlov cysts', 'Tarlov cyst', 'sacral neural cysts', 'sacral perineural cysts', 'perineural cysts']",,,65250,,,,1001858,D052958,,,,
mondo:0019002,Lhermitte-Duclos disease,"['dysplastic cerebellar gangliocytoma', 'LDD', 'dysplastic gangliocytoma of the cerebellum', 'dysplastic gangliocytoma of cerebellum']",,,65285,C0391826,,C8419,,,,,,
mondo:0019003,multiple endocrine neoplasia type 2,"['multiple endocrine neoplasia type 2', 'MEN2']",,,653,CN073359,"['0.1702', '0.474', '-0.1416', '-0.188', '-0.0736', '0.2788', '0.3599', '0.4927', '-1.176', '-0.0818', '0.2637', '0.2927', '-0.3135', '0.09924', '-0.5312', '0.5005', '-0.10065', '-0.539', '-0.2172', '0.2233', '0.2573', '-0.104', '0.5044', '-0.09155', '0.954', '0.941', '-0.024', '0.1914', '-0.1387', '-0.5693', '0.2463', '0.08813', '0.5117', '-0.00755', '0.1566', '-0.3557', '-0.483', '0.3142', '-0.05862', '-0.0282', '0.482', '-0.828', '0.9453', '-0.666', '0.6704', '0.1459', '-0.03278', '0.3381', '-0.3254', '-0.2612', '-0.4136', '0.4688', '0.2488', '-0.2455', '-0.4917', '-0.2808', '0.1536', '-0.1545', '0.1022', '0.005764', '0.5483', '0.07965', '-0.01765', '0.1866', '-0.86', '0.03323', '0.4177', '0.11163', '-0.2194', '0.4087', '0.271', '-0.3962', '0.281', '-0.671', '0.2825', '-0.2412', '-0.4937', '0.0556', '-0.0608', '-0.2637', '0.2734', '-0.1421', '-0.3083', '-0.587', '-0.506', '0.1167', '0.05872', '0.01312', '0.3596', '0.04752', '0.02675', '0.05872', '0.3362', '-0.3132', '0.9155', '-0.09406', '-0.01213', '-0.277', '0.0922', '0.5845']",C123329,,,258.02,,10028191,
mondo:0019004,kidney Wilms tumor,"['embryonal nephroma', 'Wilms tumour', 'renal embryonic tumor', 'nonanaplastic renal Wilm^s tumor', 'adult nephroblastoma', 'nephroblastoma', 'childhood renal Wilms tumour', 'Wilms tumor of the kidney', 'childhood renal Wilms tumor', 'nephroblastoma, malignant', 'nonanaplastic renal Wilm^s tumour', 'renal Wilms^ tumor', 'kidney Wilms tumor', 'Wilms tumor', 'Wilms^ tumour of the kidney', 'renal embryonic tumour', 'renal Wilms^ tumour', 'Wilms^ tumour', 'Wilms^ tumor', 'renal Wilms tumour', 'Wilms tumour of the kidney', 'renal Wilms tumor', 'Wilms^ tumor of the kidney', 'childhood renal Wilms^ cancer', 'adult renal Wilms^ tumour']",5176,,654,C0027708,"['0.03714', '-0.0984', '-0.11255', '-0.1953', '0.0429', '0.2607', '0.547', '0.613', '-0.5923', '-0.1337', '-0.05582', '0.2307', '0.0695', '0.6685', '-0.3896', '-0.843', '-0.3855', '-0.372', '0.2664', '-0.1382', '-0.3564', '-0.775', '0.996', '-0.744', '0.01514', '-0.05234', '-0.02594', '0.4136', '0.1237', '0.4006', '0.6455', '0.1566', '0.594', '-0.3486', '0.2532', '0.5405', '-0.3098', '0.1604', '0.09454', '0.387', '-0.3445', '-0.2192', '0.7603', '-0.28', '-0.2457', '0.2058', '-0.2399', '-0.3545', '0.3687', '0.2236', '0.6094', '-0.0998', '0.162', '0.03714', '-0.3596', '0.001422', '0.013504', '-0.07983', '-0.592', '0.08795', '0.591', '0.3618', '0.2344', '-0.08466', '0.03265', '-0.277', '0.6523', '0.08124', '0.01182', '0.1958', '0.2693', '-0.3076', '0.1459', '-0.2593', '0.2651', '0.1166', '-0.316', '0.03958', '-0.12415', '-0.9175', '-0.396', '-0.03384', '0.5044', '-0.0807', '-0.427', '-0.5796', '0.2615', '0.2664', '-0.0897', '-0.3115', '-0.0928', '-0.02623', '-0.1979', '0.01653', '1.32', '-0.4724', '0.3809', '-0.865', '0.0982', '-0.0812']",C40407,,,,,10029145,
mondo:0019005,nephronophthisis,"['medullary cystic disease', 'nephronophthisis', 'nephronophthisis (disease)', 'medullary cystic kidney']",12712,,655,C2939174,"['0.3308', '-0.3298', '0.1655', '0.2583', '-0.2269', '-0.0806', '-0.513', '0.794', '-0.3188', '-0.3655', '-0.4429', '-0.4675', '-0.4346', '0.4358', '0.6235', '-0.3833', '0.1995', '-0.2229', '0.06805', '-0.268', '0.2705', '-0.1115', '0.717', '0.02438', '0.4993', '-0.4126', '0.1665', '0.02927', '-0.2837', '0.2008', '0.3064', '-0.2233', '0.3704', '0.4785', '0.4294', '-0.01921', '-0.3408', '0.1017', '-0.01671', '0.1133', '-0.274', '0.101', '0.62', '-0.0716', '-0.1184', '-0.724', '-0.2715', '-0.287', '-0.1865', '0.1117', '0.0699', '-0.11993', '-0.4456', '-0.878', '-0.03128', '-0.7744', '0.563', '-0.2322', '-0.8374', '0.0001258', '0.1649', '0.179', '-0.1677', '-0.1528', '0.0851', '-0.941', '0.4258', '0.07214', '-0.4358', '0.11896', '-0.212', '-0.1312', '0.3416', '0.1222', '0.4983', '-0.4224', '0.4553', '0.228', '-0.503', '0.46', '-0.1304', '0.12085', '-0.1256', '0.2034', '-0.2688', '0.0961', '0.813', '-0.01991', '-0.08405', '-0.1058', '0.1068', '0.4104', '-0.552', '-0.2046', '0.684', '0.414', '0.4573', '-0.216', '-0.02899', '0.1615']",C123200,,,,,,0000090
mondo:0019006,familial idiopathic steroid-resistant nephrotic syndrome,['familial idiopathic nephrotic syndrome'],,,656,CN536255,,,,,,,,
mondo:0019007,vaginal atresia,,,,65681,,,,,,,,10046879,0000148
mondo:0019008,benign recurrent intrahepatic cholestasis,"['Summerskill-Walshe-Tygstrup syndrome', 'cholestasis, benign recurrent intrahepatic', 'Bric']",0070230,,65682,C0149841,"['0.1559', '-0.3225', '-0.153', '-0.00452', '-0.2678', '-0.3464', '0.669', '0.06158', '0.3127', '0.4634', '-0.5195', '-0.4756', '-0.2252', '0.6113', '-0.5713', '-0.3127', '-0.1583', '-0.166', '0.0875', '-1.026', '-0.01941', '-0.1061', '0.734', '-0.4414', '-0.1108', '-0.359', '0.1644', '0.573', '0.00981', '-0.4575', '0.69', '-0.08875', '-0.1727', '0.2181', '-0.589', '-0.695', '-0.442', '0.1028', '-0.369', '0.5205', '0.0004926', '-0.666', '0.759', '-0.04996', '-0.105', '-0.01404', '-0.1544', '-0.4988', '0.0822', '0.1442', '-0.012', '0.212', '-0.463', '-0.0959', '0.1316', '0.274', '-0.01288', '-0.1682', '-0.6113', '0.4556', '0.01796', '0.10516', '0.4512', '-0.2585', '0.2717', '-0.00604', '0.784', '0.7524', '0.07874', '0.926', '0.2351', '-0.03114', '0.606', '-0.384', '0.869', '0.507', '0.617', '0.4626', '0.0384', '-0.02757', '0.010735', '-0.1605', '-0.7856', '0.1095', '-0.1511', '-0.01172', '0.1282', '-0.2786', '0.1284', '-0.1527', '0.8296', '0.8696', '-0.3616', '0.4104', '0.8726', '-0.0961', '0.02057', '-0.3733', '-0.11035', '-0.4702']",,,,,,,
mondo:0019009,isolated focal cortical dysplasia,['epilepsy due to FCD'],,,65683,,"['-0.1461', '0.419', '0.1505', '-0.4575', '0.0393', '0.2776', '0.2983', '0.1439', '-0.27', '-0.06195', '-0.55', '-0.3481', '-0.495', '-0.4495', '-0.04016', '0.01249', '-0.08276', '-0.5015', '-0.3472', '-0.4333', '0.161', '-0.000295', '0.378', '0.11835', '0.1304', '0.0675', '-0.05493', '-0.0784', '-0.05093', '0.3496', '0.0348', '-0.1587', '0.665', '0.098', '0.297', '0.396', '-0.1617', '-0.2917', '0.0731', '-0.667', '0.576', '-0.3474', '-0.3298', '0.1354', '-0.148', '-0.2527', '-0.2494', '0.2383', '-0.02237', '0.1044', '0.6875', '0.1605', '0.05096', '-0.2416', '-0.252', '0.3203', '0.4', '0.0247', '-0.379', '0.10815', '-0.05276', '0.06854', '0.2542', '-0.08716', '-0.3347', '0.2032', '0.648', '0.1772', '-0.2876', '0.1622', '-0.1495', '0.5186', '-0.03638', '0.1152', '-0.1677', '0.10876', '0.5015', '0.2335', '-0.3972', '-0.467', '-0.2708', '0.1617', '0.1614', '0.1332', '0.1357', '-0.35', '0.1473', '0.63', '0.3674', '0.2896', '-0.1252', '0.3704', '0.01291', '0.0515', '0.466', '0.03677', '0.617', '-0.1138', '0.614', '0.3938']",,,,,,,
mondo:0019010,congenital isolated hyperinsulinism,"['persistent hyperinsulinemic hypoglycemia of infancy', 'chi', 'PHHI', 'hyperinsulinemic hypoglycemia familial', 'hypoglycemia hyperinsulinemic of infancy', 'hyperinsulinism familial with pancreatic nesidioblastosis', 'congenital hyperinsulinism', 'hyperinsulinism congenital']",,,657,,,C122923,,,,,,
mondo:0019011,Charcot-Marie-Tooth disease type 1,"['autosomal dominant demyelinating Charcot-Marie-Tooth disease', 'CMT1', 'hereditary motor and sensory neuropathy type 1', 'Charcot-Marie-Tooth type 1', 'Charcot-Marie-Tooth neuropathy type 1']",0050538,,65753,,,,,,,,,
mondo:0019012,Carpenter syndrome,"['ACPS2', 'acrocephalopolysyndactyly type 2', 'acrocephalopolysyndactyly type II', 'acrocephalosyndactyly, type II', 'Carpenter syndrome', 'Carpenter ^s syndrome', 'type II Acrocephalopolysyndactyly']",0060234,,65759,CN229565,"['0.01267', '-0.577', '0.2062', '-0.457', '0.3152', '-0.4211', '0.1594', '0.9478', '-0.667', '-0.5674', '-0.01733', '0.1567', '-0.1909', '0.4443', '-0.3804', '-0.0946', '0.399', '-0.2036', '-0.1748', '-0.5283', '0.04785', '0.4978', '0.2925', '-0.4382', '0.4138', '-0.01113', '-0.199', '0.25', '0.9873', '-0.3025', '0.5083', '-0.09106', '-0.04938', '0.2449', '0.013756', '-0.8296', '0.1267', '-0.5264', '0.07074', '-0.39', '-0.3079', '0.551', '0.309', '-0.2915', '0.3374', '-0.0982', '-0.0904', '0.2734', '-0.4277', '0.2908', '-0.1619', '0.2395', '0.0514', '0.0863', '-0.764', '-0.481', '-0.2512', '-0.187', '-0.07355', '0.2141', '0.242', '0.3018', '-0.01982', '0.1809', '-0.00457', '-0.1373', '0.2488', '0.899', '-0.3474', '0.3008', '-0.7866', '0.4797', '0.1083', '-0.129', '-0.10657', '-0.3594', '0.006725', '-0.3455', '-0.3193', '-0.385', '-0.05307', '0.181', '-0.409', '0.237', '0.573', '0.48', '0.2025', '-0.1731', '-0.237', '-0.081', '-0.5815', '0.632', '-0.186', '0.6147', '0.836', '-0.1311', '0.397', '-0.1703', '0.6895', '0.5']",C98873,,,,,,
mondo:0019013,non-histaminic angioedema,"['angioneurotic oedema', 'non histamine-induced angioedema', 'angioneurotic edema', 'bradykinine-induced angioedema']",,,658,CN227560,,,,,995.1,,,
mondo:0019015,omphalocele,"['omphalocele', 'eventration', 'congenital omphalocele', 'omphalocele (disease)', 'omphalocoele', 'exomphalos']",0060327,,660,C0795690,,C98997,,D006554,756.72,,10030308,0001539
mondo:0019016,maternally-inherited progressive external ophthalmoplegia,"['maternally-inherited chronic progressive external ophthalmoplegia', 'maternally-inherited CPEO']",,,663,CN924917,,,,,,H49.4,,
mondo:0019017,short fifth metacarpals-insulin resistance syndrome,,,,66518,CN205478,,,,,,,,
mondo:0019018,Tako-tsubo cardiomyopathy,"['broken-heart syndrome', 'Tako tsubo syndrome', 'Takotsubo cardiomyopathy', 'ballooning cardiomyopathy', 'stress cardiomyopathy', 'ASC', 'Takotsubo syndrome', 'broken heart syndrome', 'Tako-Tsubo syndrome', 'transient antero-apical dyskinesia', 'transient left ventricular apical ballooning syndrome', 'acute stress cardiomyopathy', 'left ventricular transient apical ballooning', 'apical ballooning syndrome', 'ampulla cardiomyopathy', 'stress-induced cardiomyopathy']",,,66529,CN205479,,C85181,1002000,D054549,429.83,,,
mondo:0019019,osteogenesis imperfecta,"['Vrolik disease', 'Vrolik^s disease', 'brittle bone disease', 'Porak and Durante disease', 'glass bone disease', 'OI', 'Lobstein^s syndrome', 'Fragilitas ossium', 'Lobstein disease', 'Osteopsathyrosis']",12347,,666,C0029434,"['0.2593', '-0.1726', '-0.0376', '-0.11505', '0.02597', '0.2272', '-0.1895', '1.101', '-0.6167', '0.1726', '-0.372', '0.1145', '0.2457', '0.1556', '0.1309', '0.465', '0.1471', '-0.0709', '0.1552', '-0.5806', '0.1296', '0.1703', '1.376', '0.2573', '-0.4756', '0.3442', '0.04462', '-0.1782', '-0.445', '0.1271', '0.10376', '-0.2554', '0.00651', '0.289', '-0.06647', '-0.5776', '-0.6753', '-0.658', '-0.2014', '-0.264', '-0.13', '-0.7275', '0.783', '-0.2576', '0.1748', '-0.8784', '0.0454', '0.5786', '0.3506', '-0.002192', '0.2815', '-1.113', '0.3325', '-0.281', '-0.252', '-0.774', '-0.754', '-0.232', '-0.14', '0.3335', '-0.2208', '-0.4631', '-0.272', '-0.3274', '-0.7', '0.4993', '0.3762', '0.2137', '-0.4062', '0.5146', '0.2372', '-0.3357', '-0.1371', '-0.84', '0.2937', '-0.02124', '-0.3145', '-0.4067', '0.2878', '-0.1324', '0.05576', '-0.2727', '-0.6416', '0.8486', '-0.711', '0.4336', '0.01816', '-0.04358', '0.751', '-0.3245', '-0.0064', '0.1075', '-0.374', '0.05603', '0.3228', '-0.01874', '0.06152', '-0.3152', '0.2279', '-0.408']",C26837,,D010013,756.51,Q78.0,10031243,
mondo:0019020,PANDAS,"['paediatric autoimmune disorders associated with Streptococcus infections', 'pediatric autoimmune neuropsychiatric disorders associated with Streptococcus infections', 'pediatric autoimmune disorders associated with Streptococcus infections', 'pediatric autoimmune neuropsychiatric disorder associated with Streptococcus', 'paediatric autoimmune neuropsychiatric disorders associated with streptococcal infections', 'paediatric autoimmune neuropsychiatric disorder associated with Streptococcus', 'paediatric autoimmune neuropsychiatric disorders associated with Streptococcus infections', 'pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections']",,,66624,CN205481,,,,C537163,,,,
mondo:0019022,sensorineural hearing loss-early graying-essential tremor syndrome,,,,66633,CN205488,,,,,,,,
mondo:0019023,cutaneous mastocytosis,"['cutaneous (skin) mastocytosis', 'cutaneous mastocytosis', 'mastocytosis, cutaneous', 'cutaneous mastocytosis (disease)', 'mastocytosis, systemic, somatic', 'CMCD', 'CM']",3663,154800,66646,C1136033,,C7137,1000886,D034701,,,,0200151
mondo:0019024,mast cell sarcoma,"['MCS', 'sarcoma of mast cell', 'MCSL', 'mast-cell sarcoma', 'mast cell sarcoma']",355,,66661,C0036221,,C9348,1000364,D012515,202.6,,,
mondo:0019025,extracutaneous mastocytoma,['extracutaneous mastocytoma'],4659,,66662,C0272202,,C7136,1000932,,,,,
mondo:0019026,autosomal recessive osteopetrosis,"['osteopetrosis (disease), autosomal recessive', 'autosomal recessive osteopetrosis', 'infantile malignant osteopetrosis', 'OPTB', 'malignant osteopetrosis', 'autosomal recessive malignant osteopetrosis']",,,667,,"['-0.577', '0.3745', '0.1987', '-0.2817', '-0.02441', '0.3225', '-0.2383', '1.354', '-0.1099', '-0.1932', '-0.3235', '-0.4656', '-0.451', '0.04425', '0.2318', '-0.1212', '-0.127', '-0.557', '-0.2057', '-0.9443', '0.304', '-0.2646', '0.9873', '0.07837', '-0.01189', '0.4404', '-0.07605', '-0.4272', '-0.3123', '-0.3035', '0.2363', '0.10065', '0.3535', '0.3186', '0.009056', '-0.0644', '-0.2081', '-0.6475', '0.04434', '-0.1301', '-0.2158', '0.0712', '0.2023', '-0.10046', '-0.2517', '0.05124', '0.03123', '-0.618', '0.3677', '0.1752', '0.4104', '-0.1128', '0.7095', '0.2361', '0.2196', '0.0637', '0.2676', '0.6504', '-0.0714', '0.04538', '0.177', '0.08374', '-0.268', '-0.0842', '0.03986', '-0.277', '0.3608', '1.0205', '-0.5273', '0.3354', '0.010704', '-0.2048', '0.2153', '-0.0709', '-0.2183', '-0.3171', '-0.007797', '0.649', '0.2192', '-0.5874', '0.2908', '-0.6562', '-0.2783', '0.726', '-0.415', '-0.3823', '0.571', '-0.086', '-0.2418', '0.4058', '-0.1323', '-0.41', '-0.4392', '-0.004997', '0.483', '0.5684', '0.758', '-0.2141', '0.322', '-0.3687']",C129733,,,,,,
mondo:0019027,otopalatodigital syndrome,"['type 2 (Andre syndrome)', 'oto-palatal-digital syndrome']",,,669,CN205496,"['0.04074', '0.2106', '0.3977', '-0.2017', '0.521', '-0.3564', '-0.12006', '0.3586', '-0.1456', '-0.2524', '-0.1755', '-0.4119', '0.1752', '0.12463', '-0.06995', '0.1613', '-0.2468', '0.1272', '-0.2362', '-0.3167', '-0.000811', '0.2277', '0.928', '-0.4038', '0.1378', '0.1001', '-0.3328', '-0.529', '0.2505', '-0.408', '0.4194', '-0.2864', '0.1699', '0.1946', '0.1671', '-0.1672', '-0.2422', '-0.342', '-0.509', '-0.1483', '0.1453', '-0.4734', '-0.10876', '-0.2052', '0.1863', '-0.4001', '-0.0736', '0.5635', '-0.4502', '-0.03084', '0.2092', '-0.257', '-0.3044', '-0.0339', '-0.4602', '-0.2544', '-0.07135', '-0.3542', '-0.4143', '0.334', '0.1539', '-0.03041', '-0.12164', '0.3257', '-0.0842', '-0.2091', '-0.09064', '-0.1115', '-0.3555', '0.1924', '-0.2467', '-0.2095', '0.3447', '-0.1772', '0.2489', '0.1626', '-0.2588', '-0.04733', '-0.4282', '-0.2742', '0.3', '0.1814', '0.001904', '0.4082', '-0.1027', '0.3887', '0.03134', '0.4607', '0.2747', '0.09985', '0.06714', '0.4585', '0.3037', '0.1814', '0.515', '-0.01298', '0.2861', '-0.4915', '0.1937', '0.09503']",,,,,,,
mondo:0019028,amoebiasis due to Entamoeba histolytica,,,,67,C2930799,,,,C531613,,,,
mondo:0019029,segmental odontomaxillary dysplasia,['SOD'],,,67039,,,,,,524.89,,,
mondo:0019031,thrombocytopenia with congenital dyserythropoietic anemia,"['X-linked congenital dyserythropoietic anemia with thrombocytopenia', 'X-linked congenital dyserythropoietic anaemia with thrombocytopenia', 'congenital dyserythropoietic anaemia with thombocytopenia', 'congenital dyserythropoietic anemia with thombocytopenia', 'XDAT']",,,67044,C4302508,"['-0.0898', '0.274', '-0.5713', '0.101', '0.2852', '0.2473', '-0.2996', '0.391', '0.1081', '-0.634', '0.597', '-0.007374', '0.6255', '0.587', '-0.8237', '0.11346', '-0.9497', '0.1598', '-0.3997', '-0.456', '-0.119', '-0.5835', '0.4805', '-0.2795', '0.7935', '-0.0577', '-0.1598', '-0.2225', '0.8726', '0.08594', '-0.1072', '-0.1677', '0.6035', '1.031', '0.538', '-0.5425', '-0.8145', '-0.5854', '0.542', '0.0952', '-0.3877', '0.09216', '0.2167', '-0.7446', '-0.314', '-0.7764', '0.07697', '0.2598', '0.2869', '-0.4878', '0.393', '0.2988', '0.988', '-0.1693', '0.4998', '-0.2411', '0.2344', '0.1819', '-1.055', '-0.2003', '0.04562', '0.25', '-0.1123', '-0.4893', '0.1385', '0.341', '0.2382', '0.598', '-0.522', '0.8696', '0.647', '-0.148', '-0.666', '-0.6045', '0.449', '1.102', '0.1915', '0.1199', '0.06165', '0.11163', '-0.1276', '0.01446', '0.0381', '-0.0205', '-0.00819', '-0.3027', '-0.647', '0.2416', '0.566', '-0.1761', '0.6196', '0.506', '-0.4421', '0.091', '0.4404', '0.8906', '-0.0191', '0.12164', '0.6875', '-0.4546']",,,,,,,
mondo:0019032,X-linked intellectual disability with isolated growth hormone deficiency,['MRGH'],,,67045,C1848068,,,,,,E23.0,,
mondo:0019033,primary cutis verticis gyrata,,,,671,C0263417,,,,,757.39,,,
mondo:0019034,accessory pancreas,['pancreas accessorium'],,,674,,,,,C536003,,,,
mondo:0019035,pancreatoblastoma,"['pancreatoblastoma (morphologic abnormality)', 'PB']",6823,,677,C0334489,,C4265,1000446,C537162,,,,
mondo:0019036,amoebiasis due to free-living amoebae,,,,68,CN205519,,,,,,,,
mondo:0019037,progressive supranuclear palsy,"['progressive supranuclear ophthalmoplegia', 'familial progressive supranuclear palsy (type)', 'PSP syndrome', 'supranuclear palsy, progressive', 'Steele-Richardson-Olszewski syndrome']",678,,683,CN205522,"['0.207', '1.254', '-0.02274', '0.1774', '-0.589', '-0.5938', '0.4978', '0.4143', '-1.271', '-0.01698', '0.8276', '-0.0629', '-0.452', '0.5234', '0.2986', '-0.2488', '-0.2812', '-0.753', '-0.5586', '-0.1825', '-0.02803', '0.2615', '-0.09973', '0.1052', '0.3057', '0.0977', '0.3445', '-0.09894', '-0.529', '0.909', '0.3267', '-0.04892', '0.2666', '-0.087', '0.2817', '-0.248', '0.7285', '0.1487', '-0.258', '-0.848', '1.053', '-0.2144', '-0.114', '0.3313', '0.6675', '-0.187', '0.04828', '-0.4338', '-0.02615', '0.6284', '-0.05573', '0.582', '-0.1346', '-1.156', '0.2345', '-0.7554', '-0.08777', '-0.1439', '0.0377', '-0.277', '0.2479', '-0.3623', '-0.536', '-0.485', '-0.323', '0.569', '0.232', '-0.3171', '-0.1829', '0.9565', '-0.1698', '-0.222', '0.1311', '-0.6797', '0.6045', '0.6074', '-0.2137', '0.08777', '-0.04523', '0.391', '0.2512', '-1.373', '0.09686', '0.745', '-0.09814', '-0.5464', '0.443', '0.0478', '0.6177', '-0.6377', '0.7153', '0.3765', '-0.707', '0.985', '0.1539', '1.111', '0.05185', '-0.3357', '0.399', '0.1304']",C85028,,D013494,333.0,,10036813,
mondo:0019040,chromosomal disorder,"['disorder, chromosomal', 'disorders, chromosomal', 'chromosome abnormality disorders', 'disorder, chromosome', 'chromosome disorder', 'autosomal chromosome disorder', 'chromosomal disorder', 'disorder, chromosome abnormality', 'autosomal chromosome disorders', 'chromosomal disorders', 'disorders, chromosome', 'chromosomal disease', 'chromosome abnormality disorder', 'chromosome disorders, autosomal', 'chromosome disorder, autosomal']",0080014,,68335,,,C34470,,D025063,758.89,Q90-Q99,,
mondo:0019042,multiple congenital anomalies/dysmorphic syndrome,['MCAHS'],,,68341,,,,,,,,,
mondo:0019044,tumor of hematopoietic and lymphoid tissues,,,,68347,CN205528,,,,,,,,
mondo:0019046,leukodystrophy,"['leukodystrophy, hypomyelinating', 'HLD', 'hypomyelinating leukodystrophy', 'hypomyelinating leukoencephalopathy']",10579,,68356,CN228461,"['0.0668', '0.2598', '0.2046', '0.3755', '0.0648', '-0.0768', '-0.03284', '0.03702', '-0.6265', '0.1809', '-0.4756', '-0.3967', '0.113', '0.6797', '0.5205', '-0.1844', '-0.2805', '-0.199', '-0.364', '-0.3245', '0.08685', '-0.0633', '-0.2786', '0.0444', '-0.0435', '-0.5234', '0.01339', '0.0862', '-0.471', '0.4048', '0.0754', '0.22', '0.3481', '0.1667', '0.2488', '-0.261', '0.09796', '0.1293', '0.4514', '-0.433', '0.187', '0.03763', '0.0755', '0.2932', '0.157', '-0.481', '-0.0723', '0.1368', '0.4944', '-0.03607', '0.1997', '0.0702', '0.181', '0.1067', '0.205', '-0.0986', '-0.03134', '0.478', '-0.317', '0.2832', '0.1498', '0.2362', '0.516', '0.3013', '-0.544', '0.1802', '0.11487', '0.414', '-0.2458', '0.744', '0.10925', '0.1461', '0.08716', '-0.3381', '0.4202', '0.303', '-0.2075', '0.841', '-0.2837', '-0.4294', '-0.1951', '-0.5664', '-0.2883', '0.3174', '-0.3801', '-0.2173', '0.4229', '0.1013', '0.3762', '0.1385', '0.2402', '-0.02203', '-0.5356', '0.2974', '-0.09546', '0.3955', '0.3413', '-0.4446', '0.4236', '0.07776']",C61253,,,330.0,,10024381,
mondo:0019050,inherited hemoglobinopathy,"['hemoglobinopathies', 'Hemoglobinopathies / iron metabolism', 'hereditary hemoglobinopathy', 'hemoglobinopathy']",2860,,68364,C1960031,,C3092,,D006453,282.7,D58.1,10060892,
mondo:0019052,inborn errors of metabolism,"['inborn error of metabolism', 'inborn errors of metabolism', 'inherited metabolic disorder', 'metabolic hereditary disorder', 'inborn metabolic disorder', 'inherited disorders of metabolism', 'congenital metabolic disorder', 'inborn disorders of metabolism', 'inherited disorder of metabolism', 'rare inborn errors of metabolism', 'inborn metabolism disorder', 'rare metabolic disease', 'congenital metabolism disorder', 'hereditary metabolic disease']",655,,68367,C0025521,,C34816,,D008661,,,10062018,
mondo:0019053,peroxisomal disease,"['peroxisomal disease', 'peroxisomal disorder', 'peroxisomal function disorder', 'disorder of peroxisomal function']",906,,68373,C0282528,,C85005,,,277.89,,,
mondo:0019054,congenital limb malformation,,,,68378,,,,,,,,,
mondo:0019056,neuromuscular disease,"['nerve and muscle disorder', 'neuromuscular disease']",440,,68381,C0027868,,,1001902,D009468,358.9,,10029323,
mondo:0019060,bone neoplasm,"['primary malignant neoplasm of bone', 'rare bone tumour', 'osseous neoplasm', 'primary bone cancer', 'tumour of the bone', 'bone tissue tumour', 'bone tumour', 'bone neoplasms', 'bone tumours', 'bone tumor', 'tumor of the bone', 'osseous tumour', 'osseous tumor', 'tumour of bone tissue', 'bone neoplasm', 'tumor of bone tissue', 'bone tumors', 'neoplasm of the bone', 'neoplasm of bone tissue', 'tumour of bone', 'bone tissue tumor', 'neoplasm of bone', 'tumor of bone', 'rare bone tumor']",,,68411,,,C9343,,,,C40-C41,,
mondo:0019063,vascular anomaly,['vascular anomaly or angioma'],,,68419,,,,,,,,,
mondo:0019064,hereditary spastic paraplegia,"['familial spastic paraparesis', 'Strumpell-Lorrain disease', 'hereditary spastic paraparesis', 'SPG', 'HSP', 'spastic paraplegia', 'FSP', 'Strümpell-Lorrain disease', 'French settlement disease', 'familial spastic paraplegia']",2476,,685,,,C140267,,D015419,334.1,G11.4,10019903,
mondo:0019065,amyloidosis,"['amyloidoses', 'amyloid', 'amyloid disease', 'amyloidosis (disease)', 'amyloidosis']",9120,,69,C0002726,,C2868,1001875,D000686,277.30,,10002022,0011034
mondo:0019067,idiopathic steroid-sensitive nephrotic syndrome,,,,69061,,,,,,,,,
mondo:0019068,congenital membranous nephropathy due to maternal anti-neutral endopeptidase alloimmunization,"['alloimmune neonatal renal disease', 'neonatal glomerulopathy due to Neprilysin alloimmunization', 'neonatal membranous glomerulopathy with maternal NEP deficiency', 'neonatal membranous glomerulopathy with maternal neutral endopeptidase deficiency', 'FMAIG', 'fetomaternal alloimmunization with antenatal glomerulopathies', 'neonatal glomerulopathy due to neprilysin alloimmunization']",,,69063,C4511239,,,,,,,,
mondo:0019071,pure hair and nail ectodermal dysplasia,"['hair-nail ectodermal dysplasia', 'PHNED', 'HNED']",0111655,,69084,,"['0.1407', '0.1909', '0.0926', '-0.1434', '0.2935', '-0.318', '-0.1116', '0.386', '-0.0427', '-0.4292', '-0.1004', '-0.1288', '-0.2563', '-0.05423', '0.0879', '0.2404', '0.467', '-0.1906', '-0.2289', '-0.4219', '-0.3577', '0.09595', '0.0926', '-0.0883', '0.0375', '0.1506', '-0.3772', '-0.01482', '0.05466', '-0.242', '0.1268', '-0.1774', '-0.07996', '0.1405', '0.1874', '-0.1354', '-0.1136', '-0.3123', '0.068', '-0.0418', '0.17', '-0.3818', '-0.1266', '-0.262', '0.02246', '-0.2632', '-0.1206', '0.1638', '-0.1116', '-0.4224', '0.0935', '-0.1083', '0.2878', '0.1718', '-0.1439', '-0.06464', '0.4263', '-0.2335', '-0.2646', '-0.2302', '0.1041', '0.1902', '0.02798', '-0.0578', '0.05542', '-0.0548', '0.1342', '0.4963', '-0.1299', '0.3906', '-0.3604', '-0.0948', '0.03738', '0.04144', '0.1669', '0.1896', '-0.163', '-0.1287', '0.1478', '-0.12', '0.1819', '0.1445', '0.2795', '0.3293', '0.1345', '0.0928', '-0.0789', '0.3464', '0.1755', '0.379', '0.2617', '0.2717', '0.2346', '0.189', '0.749', '-0.01997', '0.3616', '-0.5093', '0.2057', '0.1127']",,,,,,,
mondo:0019072,intrahepatic cholestasis,,1852,,,C0008372,,,,D002780,,,,
mondo:0019073,hypotrichosis-lymphedema-telangiectasia-renal defect syndrome,"['hypotrichosis-lymphedema-telangiectasia-renal defect syndrome', 'hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome', 'telangiectatic membranoproliferative glomerulonephritis', 'glomerulonephritis with sparse hair and telangiectases', 'HLTRS']",0111360,137940,,CN205563,,,,C536825,,,,
mondo:0019074,bilateral acute depigmentation of the iris,['BADI'],,,69736,,,,,,,,,
mondo:0019075,Bosley-Salih-Alorainy syndrome,['BSAS'],,,69737,,"['-0.064', '0.3203', '0.12476', '-0.3228', '0.4238', '-0.317', '0.2974', '-0.0105', '0.04196', '-0.8867', '-0.1134', '-0.6455', '0.04288', '-0.479', '-0.1482', '-0.294', '-0.1373', '-0.1323', '-0.4001', '-0.6367', '0.0629', '-0.2314', '-0.11743', '-0.1205', '0.3093', '-0.03006', '-0.0788', '0.05743', '0.552', '0.3318', '0.0748', '0.2354', '0.3025', '0.2396', '-0.346', '-0.38', '-0.188', '-0.01682', '0.04648', '-0.4922', '0.1945', '0.05972', '0.3499', '-0.1548', '0.4126', '-0.0863', '-0.2524', '0.278', '0.1162', '0.1926', '0.2732', '0.3838', '-0.6997', '-0.1632', '-0.0366', '-0.0339', '0.3901', '-0.1415', '-0.4233', '0.6934', '0.2426', '0.2377', '0.6143', '0.4072', '-0.2898', '-0.3772', '0.06433', '0.546', '-0.3843', '0.6787', '-0.705', '0.3972', '0.1066', '0.2141', '0.06885', '0.0704', '1.007', '0.1415', '-0.2625', '-0.4612', '-0.11304', '-0.1389', '0.2389', '0.55', '-0.00983', '0.1298', '0.2705', '0.6113', '-0.1661', '0.1482', '0.598', '0.8223', '0.1682', '-0.2322', '0.5386', '0.1268', '0.717', '-0.4985', '0.3706', '0.11005']",,,,,,,
mondo:0019076,circumscribed palmoplantar hypokeratosis,,,,69744,,,,,,,,,
mondo:0019077,warty dyskeratoma,"['follicular dyskeratoma', 'isolated follicular keratosis']",,,69745,C0334063,,C4087,,,,,10068856,
mondo:0019078,Ritscher-Schinzel syndrome,"['Dandy-Walker-like malformation with ASD', 'Dandy-Walker like malformation with atrioventricular septal defect', 'Dandy-Walker-like malformation with atrioventricular septal defect', 'cranio-cerebello-cardiac dysplasia', 'CCC dysplasia', '3C syndrome', 'Ritscher-Schinzel syndrome', 'Ritscher-Schinzel cranio-cerebello-cardiac syndrome', 'Craniocerebellocardiac dysplasia', 'Ritscher Schinzel syndrome', 'craniocerebellocardiac dysplasia']",0060565,,7,C0796137,"['-0.1383', '-0.0471', '0.202', '-0.4275', '0.5234', '-0.243', '0.4197', '0.7915', '-0.838', '-0.5054', '0.08307', '-0.9795', '-0.5884', '-0.2876', '-0.236', '-0.2062', '-0.233', '-0.5137', '0.0985', '-0.6685', '-0.0631', '0.002842', '-0.3083', '-0.0329', '-0.2393', '-0.2773', '-0.6274', '0.3296', '0.8643', '-0.2712', '0.5874', '-0.04514', '0.4297', '-0.3313', '0.02663', '-0.2917', '0.1216', '-0.1619', '-0.513', '-0.3013', '0.568', '-0.2109', '0.566', '-0.2964', '0.4128', '-0.32', '-0.02794', '0.4924', '-0.554', '-0.309', '-0.5195', '-0.174', '-0.3481', '0.321', '-0.894', '-0.2556', '0.1382', '0.2783', '-0.3064', '0.11395', '-0.3655', '-0.0834', '-0.01598', '-0.0907', '0.0852', '-0.0926', '-0.004047', '0.5444', '-0.0782', '0.4143', '-0.0878', '-0.1327', '0.09845', '-0.01932', '-0.0653', '0.2189', '-0.1866', '-0.6396', '-0.357', '0.593', '0.1278', '0.4019', '0.1223', '0.5615', '0.3967', '0.461', '0.264', '-0.1324', '0.2472', '0.1322', '-0.2803', '0.2355', '0.0094', '-0.0778', '1.332', '-0.4502', '0.5815', '0.1456', '0.5127', '0.383']",,,C535313,,,,
mondo:0019079,proximal spinal muscular atrophy,['SMA'],,,70,CN205570,"['0.5317', '-0.02327', '-0.1323', '-0.00772', '0.2786', '-0.2603', '0.4746', '0.984', '-1.058', '-0.2242', '-0.7363', '0.05267', '-0.2358', '0.605', '0.1366', '-0.3657', '-0.2441', '-0.1381', '-0.3955', '-0.962', '-0.07056', '-0.6655', '0.9546', '-0.0489', '-0.01921', '-0.1398', '-0.09576', '0.04993', '-0.6343', '-0.01903', '0.701', '0.509', '-0.1414', '-0.1831', '-0.01446', '-0.10724', '-0.2532', '-0.1672', '-0.01825', '0.4736', '-0.2402', '-0.729', '0.1289', '0.446', '0.02257', '0.533', '-0.1542', '-0.1439', '0.012764', '0.5635', '-0.734', '-0.2544', '0.12164', '-0.3403', '-0.2477', '-0.589', '-0.2183', '0.1359', '0.06885', '-0.05902', '-0.0414', '0.3875', '0.1013', '0.4846', '-0.397', '-0.04956', '0.4907', '0.0439', '-0.3674', '-0.00957', '0.2705', '-0.2382', '0.02655', '-0.1945', '0.6772', '0.2494', '-0.3843', '0.1218', '-0.213', '-0.3062', '-0.1984', '-0.2969', '-0.4446', '0.7085', '-0.4453', '-0.04474', '0.2357', '0.04755', '0.2019', '-0.4067', '-0.01604', '0.1226', '0.2112', '0.2292', '0.005657', '0.3599', '0.4348', '0.1641', '0.08405', '0.05127']",,0008929,,,,,
mondo:0019080,alopecia totalis,,,,700,C0263504,,,,,704.09,,10001766,
mondo:0019082,bullous pemphigoid,"['senile dermatitis herpetiformis', 'Old Age pemphigus', 'benign pemphigus', 'bullous pemphigoid', 'Parapemphigus']",8506,,703,C0030805,,C84389,0007187,D010391,694.5,L12.0,,
mondo:0019083,Leigh syndrome with cardiomyopathy,"['Leigh disease with myopathy', 'cardiomyopathy with myopathy due to COX deficiency', 'cardiomyopathy with hypotonia due to cytochrome C oxidase deficiency']",,,70474,CN205578,,,,,,,,
mondo:0019084,radiation proctitis,,,,70475,,,,,,569.49,K62.7,10037766,
mondo:0019085,vernal keratoconjunctivitis,"['VKC', 'Spring catarrh']",,,70476,C0022577,,,,,,H16.2,,
mondo:0019086,carcinoma of esophagus,"['cancer of esophagus', 'esophagus carcinoma', 'cancer of the esophagus', 'cancer of oesophagus', 'esophageal carcinoma', 'carcinoma of the oesophagus', 'cancer of the oesophagus', 'carcinoma of the esophagus', 'oesophagus carcinoma', 'carcinoma of esophagus', 'esophageal cancer', 'esophageal cancer, NOS']",1107,,70482,C0152018,,C3513,0002916,,,,10030155,
mondo:0019087,cholangiocarcinoma,"['cholangiosarcoma', 'bile duct cancer', 'cholangiocarcinoma', 'Cholangiocellular carcinoma', 'adult primary cholangiocellular carcinoma', 'cholangiocarcinoma, intrahepatic and extrahepatic bile ducts (adenocarcinoma)', 'cholangiocarcinoma, malignant', 'intrahepatic bile duct cancer (cholangiocarcinoma)', 'CC', 'CCA', 'Cholangiocar.- intra/extrahepatic', 'adult primary cholangiocarcinoma']",4947,,70567,C0206698,,C4436,0005221,D018281,,,10008593,
mondo:0019088,post-transplant lymphoproliferative disease,"['PTLD', 'post-transplant lymphoproliferative disorder']",,,70568,C0432487,,C4727,,,,,10051358,
mondo:0019091,bronchopulmonary dysplasia,['BPD'],11650,,70589,C0006287,,C90599,,D001997,,,10006475,
mondo:0019092,infantile apnea,['apnea of infancy'],,,70590,CN205590,,,,,,,,
mondo:0019093,immunodeficiency due to selective anti-polysaccharide antibody deficiency,['specific antibody deficiency'],,,70593,C0398711,,,,,,,,
mondo:0019094,congenital Epstein-Barr virus infection,"['antenatal EBV infection', 'mother-to-child transmission of Epstein-Barr virus infection', 'congenital EBV infection', 'antenatal Epstein-Barr virus infection']",,,70596,C4274357,,,,,,,,
mondo:0019095,plague,['Yersiniosis'],3482,,707,C0032064,,C85015,,D015009,136.8,A20,10061416,
mondo:0019098,autoimmune thrombocytopenia,,,,71203,C0242584,,,,,,,10050245,
mondo:0019100,neuromyelitis optica,"['Devic^s syndrome', 'Devic^s neuromyelitis optica', 'Devic^s disease', 'Devic disease', 'NMO', 'Devic syndrome']",8869,,71211,C0027873,,C84934,0004256,D009471,341.0,,10029322,
mondo:0019101,retinal capillary malformation,,,,71213,C0730304,,,,,,,,
mondo:0019102,dentinogenesis imperfecta-short stature-hearing loss-intellectual disability syndrome,,,,71267,CN205609,,,,,,,,
mondo:0019103,benign exophthalmos syndrome,['bes'],,,71269,C4304668,,,,,,,,
mondo:0019104,Sandifer syndrome,['Sandifer^s syndrome'],,,71272,C0338465,,C113397,,C537234,,,10066142,
mondo:0019105,renal nutcracker syndrome,"['left renal vein entrapment syndrome', 'nutcracker syndrome', 'RNS']",,,71273,C3178770,,,1001838,D059228,,,,
mondo:0019107,Rh deficiency syndrome,"['Rh-null syndrome', 'RHN', 'RH-null, regulator type', 'RHNR', 'anemia, hemolytic, Rh-null, regulator type', 'Rh-null hemolytic Anemia, regulator type', 'Rh-null disease, regulator type', 'Rh-Mod', 'Rh-null disease', 'Rh deficiency syndrome']",0050641,268150,71275,C1849387,"['-0.4185', '0.4246', '-0.1016', '0.1455', '0.03635', '-0.1265', '-0.391', '-0.04385', '0.1769', '0.03577', '0.1523', '0.06995', '0.4014', '0.1794', '0.0645', '-0.281', '-0.1907', '0.154', '-0.4373', '-0.393', '0.02658', '0.1079', '0.5146', '0.2341', '0.6797', '0.1411', '-0.02907', '-0.05', '0.05267', '0.48', '0.588', '-0.2008', '0.389', '0.8735', '0.1985', '-0.187', '-0.04013', '-0.1924', '-0.1791', '-0.886', '-0.211', '-0.325', '0.0515', '-0.523', '-0.12085', '-0.625', '-0.0716', '-0.4712', '0.5615', '-0.1014', '0.2983', '-0.6475', '0.2778', '0.4238', '-0.169', '-0.055', '-0.1091', '0.33', '-0.4011', '0.147', '-0.3516', '-0.1249', '0.3286', '-0.01033', '0.2742', '0.00925', '0.2827', '-0.03497', '-0.5596', '0.7183', '0.01651', '0.07904', '-0.523', '-0.10223', '0.10364', '0.5684', '0.173', '0.08295', '-0.1799', '-0.1654', '0.1465', '-0.1896', '0.335', '0.01239', '-0.4753', '-0.2883', '0.0968', '0.5923', '0.466', '-0.5127', '0.2864', '0.03787', '0.08905', '-0.5815', '0.5356', '0.656', '-0.1633', '-0.4685', '-0.1431', '-0.2544']",,,C562717,,,,
mondo:0019108,silent sinus syndrome,['Imploding antrum syndrome'],,,71276,C3698095,,,,,478.19,,,
mondo:0019109,CANOMAD syndrome,"['chronic sensory ataxic neuropathy with anti-disialosyl antibodies', 'chronic ataxic neuropathy ophthalmoplegia M-protein agglutination disialosyl antibodies syndrome', 'chronic ataxic neuropathy-ophthalmoplegia-IgM paraprotein-cold agglutinins-disialosyl antibodies syndrome', 'chronic sensory ataxic neuropathy with anti-dyalosyl IgM antibodies']",,,71279,C2931684,,,,C537980,,,,
mondo:0019111,familial thrombocytosis,"['thrombocythemia', 'THCYT', 'hereditary thrombocytosis disease', 'hereditary thrombocytosis', 'hereditary thrombocythemia', 'familial thrombocythemia']",,,71493,CN205627,,,,,,,,
mondo:0019112,cancer-associated retinopathy,"['paraneoplastic retinopathy', 'CAR syndrome']",,,71505,,,,,D059545,362.10,,,
mondo:0019113,benign paroxysmal torticollis of infancy,,,,71518,CN205631,,,,,,,,
mondo:0019114,psychogenic movement disorders,['psychogenic dystonia'],,,71519,C3267131,,,,,,,10072376,
mondo:0019115,obesity due to melanocortin 4 receptor deficiency,['MC4R deficiency'],,,71529,C4273958,"['-0.4824', '0.4663', '-0.04202', '0.678', '-0.2023', '-0.767', '0.0796', '0.749', '-0.1992', '-0.7227', '-0.2487', '0.366', '0.279', '0.2441', '-0.5483', '-0.4075', '-0.3865', '0.901', '-0.825', '-0.6484', '0.1332', '-0.4814', '0.4648', '-0.2942', '0.2041', '0.3738', '-0.3164', '-0.2886', '0.004013', '-0.3525', '0.4048', '-0.566', '0.391', '-0.00207', '0.01246', '-0.4885', '-0.4712', '0.092', '0.5303', '0.0633', '0.06247', '-0.3318', '-0.761', '0.2725', '0.01593', '-0.819', '0.4766', '-0.12225', '0.3381', '0.0942', '-0.4248', '-0.05637', '0.4607', '-0.1816', '-0.13', '0.7583', '-0.1761', '-0.1959', '-0.1498', '-0.5596', '0.527', '0.346', '-0.2854', '-0.521', '0.0383', '0.864', '-0.297', '0.2983', '0.3838', '0.509', '0.2905', '0.3218', '-0.246', '-0.259', '0.4937', '-0.554', '-0.2438', '0.000793', '-1.275', '0.577', '0.2607', '0.838', '0.12115', '0.12164', '0.8896', '0.6294', '0.4521', '0.1299', '0.776', '0.1633', '0.05292', '0.2119', '-0.07715', '0.4688', '0.52', '0.3977', '0.2507', '-0.4827', '-0.4216', '-0.02843']",C120394,,,,,,
mondo:0019118,inherited retinal dystrophy,"['hereditary retinal dystrophy', 'retinal dystrophy', 'fundus dystrophy', 'hereditary retinal degeneration']",8501,,71862,C0854723,"['-0.1667', '0.03503', '0.05945', '0.1636', '0.2075', '-0.3132', '-0.06647', '-0.0679', '-0.1768', '-0.3052', '0.01825', '-0.2367', '-0.01688', '0.0251', '-0.275', '-0.2979', '-0.2094', '-0.1588', '-0.0403', '-0.5596', '0.1058', '-0.2717', '0.07587', '0.2213', '-0.04904', '0.2422', '0.0898', '-0.01659', '-0.10254', '0.218', '0.3132', '0.00529', '0.00872', '-0.1586', '0.1486', '0.1584', '0.2106', '0.07263', '-0.1481', '-0.5264', '0.2788', '-0.3472', '0.024', '0.01493', '-0.0896', '-0.01688', '0.005955', '-0.009094', '0.4197', '-0.0482', '0.12103', '-0.1306', '-0.00437', '-0.1276', '-0.008865', '-0.3967', '0.4878', '0.245', '-0.6553', '-0.0755', '0.1974', '-0.1387', '0.1432', '0.2445', '-0.1686', '0.09033', '0.54', '0.3086', '-0.1259', '0.2261', '-0.2961', '-0.3315', '0.1909', '0.0341', '0.1056', '0.197', '0.04922', '0.25', '-0.2238', '-0.2322', '-0.07', '-0.1335', '0.02855', '0.4973', '-0.2808', '-0.504', '0.1082', '0.10345', '0.236', '-0.0938', '0.06305', '0.2367', '0.2122', '0.1827', '0.4116', '-0.07184', '0.206', '0.03134', '-0.3052', '0.325']",C35625,,D058499,362.75,H35.5,10038857,0000556
mondo:0019119,muscular channelopathy,"['muscle tissue channelopathy', 'channelopathy of muscle tissue']",,,98737,,,,1001899,,,,,
mondo:0019120,pili bifurcati,,,,720,,,,,,,,,
mondo:0019121,pneumocystosis,"['PJP', 'Pneumocystis', 'pneumocystosis pneumonia', 'PCP', 'Pneumocystis carinii pneumonia', 'Pneumocystis jirovecii pneumonia', 'Pneumocystis pneumonia', 'pulmonary pneumocystosis', 'pneumocystosis']",11339,,723,C1535939,,C3334,0007448,D011020,136.3,B59,,
mondo:0019122,idiopathic acute eosinophilic pneumonia,"['pulmonary infiltrates with eosinophilia', 'Loeffler^s pneumonia', 'Löffler syndrome', 'Loeffler syndrome', 'Loffler syndrome', 'Loffler^s syndrome', 'IAEP']",9503,,724,CN227574,,C35301,,,,,,
mondo:0019123,continuous spikes and waves during sleep,"['continuous spikes and waves during slow-wave sleep', 'CSWSS syndrome', 'epileptic encephalopathy with continuous spike-and-wave during slow sleep', 'CSWS']",,,725,CN205644,"['0.3674', '-0.02663', '-0.04355', '-0.271', '-0.5547', '-0.09033', '1.351', '0.918', '-0.7114', '0.0562', '-0.712', '0.1437', '0.4475', '0.06067', '-0.1664', '-0.2343', '-0.3745', '-0.3108', '-0.0937', '-0.8965', '0.0923', '0.3342', '0.9087', '-0.3186', '0.2659', '-0.376', '-0.3135', '-0.319', '-0.8433', '0.4639', '0.4995', '-0.06476', '0.3835', '0.4631', '0.1062', '0.2673', '0.2358', '-0.82', '-0.07', '-0.0892', '0.5835', '0.1081', '-0.4038', '0.1615', '0.542', '-0.2114', '-0.418', '0.1874', '0.099', '0.9976', '-0.073', '0.3972', '-0.37', '-0.1527', '-0.05173', '0.5664', '0.622', '-0.511', '-0.3542', '0.3833', '-0.1963', '0.1638', '0.3833', '0.07196', '-0.4229', '-0.10614', '0.1377', '-0.003914', '-0.291', '0.539', '0.3728', '0.3213', '-0.0244', '0.0004027', '-0.0091', '-0.1121', '0.004215', '-0.3015', '-0.6714', '-0.2625', '0.42', '0.634', '0.1023', '-0.1699', '0.363', '-0.08795', '0.126', '0.1759', '0.3867', '0.4785', '-0.0345', '0.2651', '-0.2974', '0.2964', '0.09314', '0.2378', '0.4495', '-0.5513', '0.2317', '-0.4768']",,,,,,,
mondo:0019124,microscopic polyangiitis,"['microscopic polyarteritis', 'Micropolyangiitis', 'MPA']",,,727,C2347126,,C70549,1000784,D055953,,M31.7,10063344,
mondo:0019125,relapsing polychondritis,"['chronic atrophic polychondritis', 'recurrent polychondritis', 'chondromalacia, systemic']",2556,,728,C0032453,,C157268,1001148,D011081,733.99,M94.1,10038304,
mondo:0019126,intractable diarrhea of infancy,['IDI'],,,73014,,,,,,,,,
mondo:0019127,polymyositis,"['polymyositis', 'PM']",0080745,,732,C0085655,,C26925,0003063,D017285,710.4,M33.2,10036102,
mondo:0019128,mullerian aplasia,"['Mullerian duct failure', 'Müllerian duct failure', 'aplasia of the Müllerian ducts', 'aplasia of the Mullerian ducts', 'Müllerian aplasia']",,,73217,,,,,C537371,,,,
mondo:0019129,global developmental delay-osteopenia-ectodermal defect syndrome,,,,73223,CN227576,,,,,,,,
mondo:0019130,tubular renal disease-cardiomyopathy syndrome,,,,73224,CN205654,,,,,,,,
mondo:0019131,ossification anomalies-psychomotor developmental delay syndrome,,,,73230,CN227577,,,,,,,,
mondo:0019132,spinal muscular atrophy-Dandy-Walker malformation-cataracts syndrome,,,,73245,CN205656,,,,,,,,
mondo:0019133,visceral neuropathy-brain anomalies-facial dysmorphism-developmental delay syndrome,,,,73246,CN205657,,,,,,,,
mondo:0019134,central neurocytoma,"['CNC', 'Neurolipocytoma', 'central neurocytoma (WHO grade II)']",14174,,73256,C0206719,,C3791,1000856,D018306,,,,
mondo:0019136,Zygomycosis,['mucormycosis'],8485,,73263,C0043541,,C77212,0007380,D020096,117.7,B46,10061418,
mondo:0019137,non-24-hour sleep-wake syndrome,"['circadian rhythm sleep disorder, free-running type', 'circadian rhythm sleep disorder, free running type', 'non-24', 'non 24 hour sleep wake disorder', 'hypernychthemeral syndrome']",,,73267,,,,,,,G47.24,,
mondo:0019138,bleeding diathesis due to a collagen receptor defect,,,,73271,,"['-0.71', '-0.1277', '0.0891', '-0.2268', '-0.0808', '0.01329', '-0.0002623', '0.07043', '0.1309', '0.295', '0.02528', '-0.0664', '0.2102', '-0.0832', '-0.03333', '-0.344', '-0.01663', '0.05307', '-0.1317', '-0.5874', '0.0495', '-0.02678', '0.4036', '-0.08856', '0.01011', '-0.0907', '0.02644', '0.1544', '0.11444', '-0.06726', '0.03708', '0.1235', '0.3184', '0.359', '-0.1553', '-0.484', '-0.06335', '0.08', '-0.2079', '-0.5703', '0.3245', '-0.1033', '0.0441', '-0.0771', '-0.2305', '-0.2177', '-0.2439', '-0.272', '0.3481', '0.2676', '-0.0115', '-0.2896', '0.2294', '0.432', '-0.4036', '0.1185', '0.1382', '-0.01715', '-0.3635', '0.0982', '0.0846', '0.2382', '-0.06396', '-0.2277', '0.1602', '0.04227', '0.2793', '0.2078', '-0.2394', '0.3396', '-0.2688', '-0.06305', '-0.10034', '-0.1879', '0.2668', '-0.0236', '0.8096', '-0.002804', '0.4167', '-0.014175', '-0.4238', '-0.2307', '0.11035', '0.1616', '-0.2705', '0.19', '0.1146', '0.5728', '0.386', '-0.3047', '0.1794', '0.4805', '-0.0721', '-0.12024', '0.511', '0.4106', '0.2847', '-0.4382', '-0.0615', '0.383']",,,,,,,
mondo:0019139,acquired hemophilia,"['hemophilia, acquired', 'acquired hemophilia']",,,73274,C1096116,,,,C536392,,D68.311,10053745,
mondo:0019140,acute ackee fruit intoxication,"['acute intoxication by Blighia sapida', 'Jamaican vomiting sickness', 'Jamaican vomiting syndrome', 'ackee poisoning']",,,73423,,,,,C537562,988.2,,,
mondo:0019141,porokeratosis of Mibelli,,,,735,C0949506,"['0.1592', '-0.01738', '-0.674', '-0.2778', '0.5605', '-0.1506', '0.3289', '-0.08594', '-0.2036', '-0.525', '0.616', '0.2173', '0.274', '0.1029', '-0.10626', '0.2932', '0.09296', '-0.5093', '0.11786', '-0.676', '-0.4478', '-0.7354', '0.929', '-0.3335', '-0.3281', '0.0459', '-0.7744', '-0.168', '-0.05328', '-0.011475', '0.1416', '-0.741', '0.3354', '0.03577', '0.166', '0.5073', '-0.396', '-0.236', '-0.146', '-0.2112', '0.02534', '-0.8457', '0.5415', '-0.2966', '0.1967', '-0.1129', '-0.44', '-0.2439', '0.1273', '0.0294', '-0.01188', '-0.0713', '0.00993', '-0.1016', '-0.6836', '-0.01689', '0.2094', '0.04507', '-0.636', '-0.404', '-0.03004', '0.04797', '-0.5713', '-0.01765', '-0.1063', '0.3374', '0.5527', '0.5156', '0.5083', '0.8076', '0.09204', '-0.2472', '-0.2869', '0.3105', '-0.0914', '-0.1626', '-0.07745', '-0.562', '-0.4355', '-1.279', '-0.2207', '-0.2418', '0.1312', '0.2175', '-0.1904', '-0.6567', '-0.3352', '-0.2827', '0.272', '0.1342', '0.1737', '0.0836', '-0.1555', '0.376', '0.507', '-0.0722', '0.12164', '-0.8022', '0.02544', '-0.2644']",,,,757.39,,,
mondo:0019142,inherited porphyria,"['hereditary porphyria', 'porphyria', 'disorder of porphyrin and hem metabolism', 'Hematoporphyria', 'Porphyrinopathy', 'disorder of porphyrin metabolism', 'disorder of porphyrin and heme metabolism']",13268,,738,C0032708,,C97096,,D011164,277.1,,10061356,
mondo:0019143,angiostrongyliasis,,0050256,,74,C0392662,,C128394,,C536369,128.8,,10069517,
mondo:0019144,hereditary thrombophilia due to congenital protein S deficiency,"['autosomal recessive thrombophilia due to congenital protein S deficiency', 'severe hereditary thrombophilia due to congenital protein S deficiency']",0111905,,743,,"['-0.1461', '-0.09375', '-1.069', '-0.5264', '0.0664', '-0.1772', '0.03244', '0.1868', '-0.3167', '-0.5537', '-0.3184', '0.216', '0.6875', '0.0694', '-0.536', '-0.1361', '-0.4287', '-0.252', '-0.4011', '-0.595', '0.2433', '-0.542', '0.9297', '0.3655', '-0.608', '0.1415', '0.00934', '0.3284', '0.3938', '0.1263', '0.2864', '0.317', '0.3984', '0.07684', '-0.02711', '-0.1859', '0.1569', '-0.4055', '0.0641', '-0.0785', '0.063', '0.238', '0.7383', '-0.007996', '0.08594', '0.1774', '-0.1267', '0.3662', '0.6694', '0.633', '-0.2183', '-0.278', '-0.1164', '-0.419', '-0.5884', '0.3145', '0.5664', '-0.403', '-0.3938', '0.1583', '-0.2123', '0.2434', '0.5425', '-0.3367', '0.2283', '0.528', '0.4648', '0.4321', '-0.1991', '0.2756', '-0.1504', '-0.1197', '-0.786', '-0.2522', '0.177', '0.1578', '0.847', '0.11285', '0.1364', '-0.1099', '-0.878', '-0.147', '0.2499', '-0.2383', '0.09827', '0.1108', '0.07043', '0.533', '0.0959', '-0.5093', '0.5693', '0.0434', '-0.2275', '-0.05948', '0.7114', '0.1901', '0.328', '-0.6743', '-0.299', '0.0735']",,,,,,,
mondo:0019145,hereditary thrombophilia due to congenital protein C deficiency,"['severe hereditary thrombophilia due to congenital protein C deficiency', 'autosomal recessive thrombophilia due to congenital protein C deficiency', 'Protein C deficiency', 'hereditary thrombophilia due to PC deficiency', 'autosomal recessive thrombophilia due to PC deficiency', 'Protein C deficiency disease', 'protein C deficiency']",3756,,745,,"['-0.08093', '-0.2961', '-1.327', '-0.5894', '0.1699', '-0.09735', '-0.1938', '0.1267', '-0.3342', '-0.3035', '-0.4526', '-0.06445', '0.701', '-0.005085', '-0.626', '-0.1119', '-0.703', '-0.3098', '-0.5527', '-0.281', '0.4458', '-0.6147', '1.0', '0.511', '-0.442', '-0.04266', '-0.1597', '0.1516', '0.295', '0.04028', '0.576', '0.3428', '0.3533', '0.1462', '0.1186', '-0.081', '0.0414', '-0.312', '-0.0734', '-0.253', '-0.001984', '0.1044', '0.6416', '0.07196', '0.06287', '0.06415', '-0.2385', '0.3264', '0.508', '0.4722', '0.08405', '-0.2808', '-0.0936', '-0.3384', '-0.814', '0.347', '0.3938', '-0.638', '-0.4949', '0.3044', '-0.528', '0.1609', '0.5415', '-0.353', '0.2172', '0.3416', '0.4507', '0.5996', '-0.2268', '0.435', '-0.0919', '0.02148', '-0.3972', '-0.0899', '0.1713', '0.3225', '0.8574', '0.2151', '0.1252', '-0.0665', '-0.917', '-0.04535', '0.3071', '-0.1348', '0.1004', '0.2834', '0.1207', '0.4707', '0.2096', '-0.4285', '0.4783', '0.1357', '-0.2053', '-0.0988', '0.3079', '0.2059', '0.2294', '-0.747', '-0.4773', '0.08105']",C99025,,D020151,,,,
mondo:0019146,inherited susceptibility to mycobacterial diseases,"['Mendelian susceptibility to atypical mycobacteria', 'idiopathic infection caused by BCG or atypical mycobacteria', 'MSMD', 'Mycobacterium caused genetic susceptibility to infections due to particular pathogens', 'Mendelian susceptibility to mycobacterial infections']",,,748,CN181681,,,,,,,,
mondo:0019147,myiasis,"['myiasis, unspecified', 'maggot infestation', 'infestation by fly larvae', 'infestation by maggots']",11080,,75110,C0027030,,C128400,0007389,D009198,134.0,,10028586,
mondo:0019148,Wolman disease,"['Wolman disease with hypolipoproteinemia and acanthocytosis', 'Wolman^s or triglyceride storage type III disease', 'liposomal acid lipase deficiency, Wolman type', 'xanthomatosis, familial', 'Wolman^s disease', 'Wolman xanthomatosis', 'lysosomal acid lipase deficiency', 'acid lipase deficiency', 'familial xanthomatosis', 'acid esterase deficiency']",14497,620151,75233,CN438428,"['-0.4753', '-0.02914', '0.1927', '-0.1333', '0.1726', '-0.2279', '-0.444', '0.3462', '0.03586', '-0.4888', '-0.7236', '-0.2251', '0.1084', '0.181', '-0.2522', '-0.8867', '-0.287', '-0.01042', '-0.4688', '-0.689', '0.5137', '-1.006', '0.6523', '-0.632', '-0.2202', '-0.2004', '-0.01701', '0.151', '-0.2888', '-0.1699', '1.074', '-0.2145', '0.02478', '0.3757', '0.06683', '-0.0867', '-0.5835', '0.2712', '0.03528', '0.00596', '-0.162', '-0.7534', '0.3208', '-0.162', '-0.389', '-0.2001', '0.02892', '-0.2029', '-0.4255', '0.11487', '0.3523', '0.11127', '0.4578', '-0.03366', '-0.0804', '-0.783', '0.1411', '0.01956', '-0.224', '0.4329', '-0.0349', '0.328', '0.1175', '-0.45', '0.176', '-0.02843', '0.2006', '-0.02092', '0.1195', '0.1727', '-0.3787', '0.1864', '0.3643', '0.3384', '0.1788', '0.592', '0.0557', '0.2329', '-0.3494', '0.043', '-0.8643', '-0.634', '-0.5454', '-0.12415', '-0.06018', '0.3613', '0.3528', '-0.164', '0.2036', '-0.063', '0.521', '-0.11035', '-0.03937', '-0.2079', '0.413', '0.6', '0.0598', '-0.639', '0.3293', '-0.5674']",C61271,,D015223,,,10053687,
mondo:0019149,cholesteryl ester storage disease,"['CESD', 'cholesterol ester storage disease']",14502,,75234,C0008384,"['-0.5146', '0.599', '0.434', '0.008484', '0.1081', '-0.4807', '-0.295', '0.1354', '-0.1315', '-0.01544', '-0.269', '0.1017', '0.0645', '0.2007', '-0.2842', '-0.7515', '-0.2086', '0.04605', '-0.4578', '-0.4253', '0.1637', '-0.7812', '0.786', '-0.1399', '-0.2157', '0.04297', '0.1204', '-0.1719', '-0.2491', '-0.3455', '0.578', '0.2957', '0.3599', '0.2137', '0.02179', '-0.4358', '-0.3499', '0.2686', '-0.01285', '-0.322', '-0.11835', '-0.3188', '0.4272', '0.2634', '-0.4485', '-0.03038', '0.2374', '-0.05814', '0.156', '0.08563', '0.1385', '0.3193', '0.395', '-0.2622', '-0.1228', '-0.6675', '0.2239', '-0.3562', '-0.54', '0.08295', '0.2216', '0.3235', '0.1884', '-0.501', '0.206', '-0.1443', '0.3591', '-0.02975', '-0.2195', '-0.04153', '-0.2588', '-0.2812', '0.3643', '0.1935', '0.0188', '-0.03253', '0.00165', '0.3887', '-0.3665', '-0.2488', '-0.3044', '-0.535', '-0.258', '-0.07935', '0.2896', '0.04114', '0.0595', '-0.1469', '0.4873', '0.01903', '0.3967', '0.2808', '-0.0769', '-0.072', '0.706', '0.513', '0.3552', '-0.273', '-0.2339', '-0.1065']",,,,,,,
mondo:0019150,familial isolated restrictive cardiomyopathy,['familial or idiopathic restrictive cardiomyopathy'],,,75249,CN205687,,,,,,,,
mondo:0019151,oligocone trichromacy,['Oligocone syndrome'],,,75378,CN205696,,,,,,,,
mondo:0019152,Oguchi disease,"['stationary night blindness, Oguchi type', 'Oguchi syndrome', 'congenital stationary night blindness, Oguchi type']",,,75382,,"['-0.928', '-0.041', '-0.4321', '0.494', '0.2236', '-0.5303', '-0.5713', '0.3357', '-0.0482', '-0.334', '0.1819', '-0.1863', '-0.5156', '-0.2468', '0.1752', '0.3848', '0.4956', '-0.223', '0.0993', '-0.7305', '-0.1362', '-0.2556', '0.08527', '0.01663', '-0.3743', '0.09705', '-0.5264', '-0.0843', '-0.4443', '0.634', '0.6797', '0.103', '-0.297', '0.2583', '-0.2598', '0.3022', '0.362', '-0.1554', '0.1744', '0.13', '0.618', '-0.37', '-0.2118', '-0.512', '-0.1123', '-0.3472', '0.08453', '-0.2404', '0.09607', '0.0405', '0.484', '-0.09454', '0.126', '-0.2827', '0.2068', '-0.215', '0.8735', '-0.4412', '-0.1135', '-0.1361', '0.4958', '0.1293', '0.1731', '-0.04593', '0.0448', '-0.03049', '0.689', '0.5576', '-0.11896', '0.8857', '-0.348', '0.0478', '0.15', '-0.04788', '0.5347', '0.1583', '-0.3257', '-0.03833', '-0.292', '0.05963', '0.5786', '-0.5586', '0.1439', '0.5586', '0.04413', '0.10126', '0.2311', '0.05078', '0.4675', '-0.01197', '0.528', '0.51', '-0.2272', '0.503', '0.8604', '-0.1918', '-0.3909', '-0.3372', '-0.5273', '-0.03091']",,,C537743,,,,
mondo:0019153,brain malformation-congenital heart disease-postaxial polydactyly syndrome,['Goossens-Devriendt syndrome'],,,75389,C4303545,,,,,,,,
mondo:0019154,androgen insensitivity syndrome,"['DHTR deficiency', 'Goldberg - Maxwell syndrome', 'testicular feminization syndrome', 'AIS', 'androgen resistance syndrome', 'testicular feminization', 'Goldberg-Maxwell syndrome', 'dihydrotestosterone receptor deficiency', 'testicular feminization syndrome (formerly)', 'androgen insensitivity, X-linked recessive', 'androgen-insensitivity syndrome', 'AR deficiency', 'androgen insensitivity syndrome', 'androgen receptor deficiency', 'Morris syndrome', 'Feminisation - testicular']",4674,300068,754,C0039585,"['-0.4207', '0.2009', '0.345', '-0.4885', '0.6465', '-0.1931', '-0.2426', '0.1676', '-0.2104', '-0.1005', '-0.1982', '-0.4094', '0.0869', '0.223', '0.04626', '-0.04907', '0.3706', '0.07043', '-0.3418', '-0.594', '-0.3254', '-0.1171', '0.822', '-0.2039', '0.56', '0.0289', '0.3557', '0.04068', '-0.02182', '-0.5693', '0.403', '0.03198', '0.3372', '0.2045', '-0.366', '-0.292', '0.02966', '0.124', '-0.5996', '-0.4517', '0.6787', '-0.2072', '0.05307', '-0.3335', '0.1439', '-0.8267', '-0.1544', '0.11694', '0.03117', '0.412', '0.05905', '-0.866', '-0.4146', '0.311', '-0.1997', '0.1401', '0.374', '-0.2417', '-0.914', '0.2566', '-0.2915', '0.4058', '0.0851', '0.5264', '0.02605', '0.3188', '0.2756', '0.005886', '-0.468', '0.09125', '-0.2542', '0.1962', '0.1654', '-0.09753', '0.3008', '-0.2157', '0.1163', '0.1624', '-0.6694', '-0.4644', '0.2673', '0.643', '0.1615', '-0.08484', '0.04257', '-0.1323', '-0.1119', '-0.05716', '0.05338', '-0.4478', '-0.073', '0.904', '-0.3', '-0.405', '0.684', '-0.116', '0.1527', '-0.4937', '-0.2047', '0.0629']",C27226,,D013734,259.8,,10056292,
mondo:0019155,Leydig cell hypoplasia,"['46,XY DSD due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency', 'Male pseudohermaphroditism due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency', 'LH resistance due to LH receptor deactivation', '46,XY DSD due to LH resistance or LHB deficiency', 'Male pseudohermaphroditism due to LH resistance or LHB deficiency', '46,XY disorder of sex development due to luteinizing hormone resistance or luteinizing hormone beta subunit deficiency', '46,XY disorder of sex development due to LH defects', 'Male hypergonadotropic hypogonadism due to LHCGR defect', 'Leydig cell agenesis', '46,XY disorder of sex development due to LH resistance or LHB deficiency']",0112259,,755,,"['-0.3591', '0.0148', '0.03598', '-0.1315', '0.2373', '-0.0878', '-0.2046', '-0.2101', '-0.5913', '-0.5635', '0.01211', '-0.489', '-0.2612', '0.6978', '0.3945', '0.1197', '0.1626', '0.106', '-0.312', '-0.3796', '-0.7856', '0.0765', '0.756', '-0.09064', '0.524', '-0.3188', '0.1559', '0.2119', '0.404', '-0.2517', '0.8887', '-0.08386', '0.2925', '-0.3916', '-0.1946', '-0.3608', '0.07465', '0.3096', '0.05383', '-0.0918', '0.5854', '-0.1769', '-0.252', '-0.01345', '0.11664', '-0.9316', '-0.4421', '-0.02422', '0.3716', '0.238', '0.187', '-0.4126', '-0.2267', '0.2798', '-0.3342', '0.6743', '-0.1223', '-0.2898', '-0.3835', '0.4902', '-0.244', '0.03062', '0.1306', '0.3552', '0.0927', '0.206', '0.3154', '0.3518', '-0.2277', '0.581', '-0.04144', '0.2479', '0.1881', '0.1377', '0.1664', '-0.02061', '-0.348', '-0.0754', '-0.517', '-0.4314', '0.1929', '0.4543', '0.08734', '0.10016', '-0.1466', '0.09766', '-0.26', '-0.2351', '0.4707', '-0.12256', '-0.5312', '0.3079', '-0.4358', '-0.1852', '0.333', '-0.02525', '-0.08844', '-0.5146', '0.03372', '0.2191']",,,C562567,,,10024406,
mondo:0019156,angioosteohypotrophic syndrome,"['Phlebectatic osteohypoplastic angiodysplasia', 'Servelle-Martorell syndrome']",,,75508,CN205707,,,,,,,,
mondo:0019157,myelodysplastic syndrome with ring sideroblasts,"['refractory anemia with ringed sideroblasts', 'refractory Anemia with Ring sideroblasts', 'Pure sideroblastic Anaemia', 'primary acquired sideroblastic anemia', 'refractory anaemia with ringed sideroblasts', 'MDS with ring sideroblasts', 'refractory Anaemia with ringed sideroblasts', 'MDS-RS', 'acquired idiopathic sideroblastic anaemia', 'RARS', 'primary acquired sideroblastic anaemia', 'refractory Anemia with ringed sideroblasts', 'Pure sideroblastic Anemia', 'AISA', 'refractory Anaemia with Ring sideroblasts', 'myelodysplastic syndrome with Ring sideroblasts', 'acquired idiopathic sideroblastic anemia']",,,75564,,,C4036,0003812,,238.72,,,
mondo:0019158,tropical endomyocardial fibrosis,"['Davies disease', 'TEMF']",,,75565,CN205710,,,,,,,,
mondo:0019159,Loeffler endocarditis,"['eosinophilic endomyocardial disease', 'eosinophilic endocarditis']",396,,75566,,,C27044,,,,,10052841,
mondo:0019160,primary progressive freezing gait,['PPFG'],,,75567,CN205712,,,,,,,,
mondo:0019161,pseudohypoaldosteronism type 1,"['PHA1B', 'PHA type 1', 'pseudohypoaldosteronism type I autosomal recessive']",,,756,C0268436,"['0.1299', '0.3057', '-0.03117', '0.2566', '-0.2468', '-0.4268', '-0.4407', '0.4758', '-0.2266', '0.144', '-0.2205', '-0.2124', '-0.2986', '0.3342', '-0.374', '-0.1323', '0.0566', '-0.04642', '0.2874', '-0.889', '0.2231', '-0.1283', '0.9907', '0.08514', '0.03232', '0.349', '0.0404', '-0.1578', '-0.2786', '-0.3145', '0.1478', '0.3613', '0.521', '0.09863', '-0.2747', '-0.3264', '-0.1714', '0.09406', '-0.65', '0.169', '0.05676', '-0.5254', '0.3938', '0.097', '0.2103', '-0.286', '0.03732', '0.4116', '-0.1735', '0.3638', '0.03976', '0.069', '0.6113', '-0.749', '-0.33', '-0.2659', '0.3713', '-0.438', '-0.3853', '0.3906', '0.2429', '-0.1666', '0.253', '-0.494', '-0.0053', '-0.11395', '0.3242', '0.2822', '-0.4395', '-0.1437', '-0.03247', '-0.3052', '0.4248', '0.04044', '0.1702', '0.00513', '-0.3826', '0.3635', '-0.2947', '0.1697', '0.2788', '0.318', '-0.2844', '-0.4553', '0.2532', '0.2197', '0.3113', '-0.2659', '0.606', '0.003479', '0.455', '0.1188', '0.155', '-0.2288', '0.635', '0.447', '0.2157', '-0.2656', '0.0729', '0.604']",C123251,,,275.8,,,
mondo:0019162,pseudohypoaldosteronism type 2,"['chloride shunt syndrome', 'mineralocorticoid resistant hyperkalemia', 'Gordon syndrome', 'familial hyperkalemic hypertension', 'Spitzer-Weinstein syndrome', 'hyperpotassemia and hypertension familial', 'pseudohypoaldosteronism, type II', 'Gordon hyperkalemia-hypertension syndrome', 'hyperkalemia-hypertension syndrome, Gordon type', 'PHAII', 'PHA2', 'hypertensive hyperkalemia']",,,757,C1449844,"['-0.195', '-0.3916', '-0.1974', '0.0662', '-0.3857', '-0.3557', '-0.2402', '0.905', '0.05307', '-0.07086', '-0.315', '-0.03574', '-0.06964', '0.6763', '0.04196', '0.1565', '0.167', '0.06287', '0.2937', '-0.8228', '0.5415', '-0.2003', '0.6143', '-0.003765', '0.545', '-0.177', '0.1509', '-0.1599', '0.237', '0.05603', '0.6606', '0.13', '0.499', '0.338', '-0.3613', '-0.7266', '-0.3896', '0.02379', '0.643', '0.06573', '-0.1159', '-0.08545', '0.713', '0.05527', '-0.01875', '-0.6587', '-0.0771', '-0.156', '-0.0795', '-0.1937', '0.06604', '0.1169', '0.1209', '-0.5796', '-0.2869', '0.1571', '0.1026', '-0.762', '-0.4155', '0.4536', '0.364', '0.02295', '0.1472', '-0.5513', '-0.2634', '-0.3481', '-0.01299', '0.3738', '-0.322', '0.1838', '-0.2123', '-0.3662', '0.354', '0.1848', '0.3987', '-0.1553', '0.07227', '-0.2725', '-0.3354', '0.3242', '0.5396', '0.27', '0.04367', '0.04028', '-0.3044', '0.8857', '0.737', '0.09106', '0.526', '0.4026', '-0.1344', '0.1742', '-0.1996', '-0.1638', '0.5425', '0.5176', '0.6133', '-0.604', '-0.3838', '0.6025']",C123252,,,588.89,,,
mondo:0019164,6q terminal deletion syndrome,,,,75857,CN205719,,,,,,,,
mondo:0019165,central precocious puberty,"['CPP', 'gonadotropin-dependant precocious puberty', 'precocious puberty, central']",0112308,,759,C0342543,,,,C562787,259.1,,,
mondo:0019167,immunoglobulin A vasculitis,"['Henoch Schonlein purpura', 'Schoenlein-Henoch purpura', 'purpura, Schonlein-Henoch', 'Henoch-Scholein purpura', 'allergic purpura', 'anaphylactoid purpura', 'purpura, autoimmune', 'autoimmune purpura', 'HSP', 'rheumatoid purpura', 'Henoch-Schonlein purpura', 'purpura rheumatica', 'vascular purpura', 'Henoch-Schoenlein purpura', 'IgA vasculitis']",11123,,761,,,C34963,1000965,D011695,287.0,,,
mondo:0019168,pyomyositis,"['myositis tropicans', 'suppurative myositis', 'PM', 'tropical pyomyositis', 'myositis purulenta tropica']",876,,764,C1704275,,C128382,1001409,D052880,040.81,,10037652,
mondo:0019169,pyruvate dehydrogenase deficiency,"['deficiency of pyruvic dehydrogenase', 'PDHC', 'PDH', 'pyruvate dehydrogenase deficiency', 'pyruvate dehydrogenase complex deficiency', 'pyruvate decarboxylase deficiency', 'pyruvate dehydrogenase complex deficiency disease']",3649,,765,,"['-0.8145', '0.668', '-0.4106', '0.3247', '-0.0677', '-0.3796', '-0.05225', '0.4927', '-0.4355', '0.2036', '-0.403', '-0.3816', '0.2047', '0.2465', '0.2031', '0.174', '0.04727', '-0.00807', '-0.897', '-0.654', '0.5215', '0.1219', '1.132', '-0.09', '-0.2395', '0.297', '-0.4385', '0.06854', '-0.02896', '-0.1298', '0.2015', '0.2068', '0.1315', '0.21', '-0.07684', '-0.201', '-0.1156', '-0.3105', '-0.5493', '0.5254', '0.3152', '-0.7344', '0.635', '-0.4707', '0.7505', '-0.561', '0.1051', '-0.0029', '0.1715', '0.4797', '-0.39', '-0.7256', '-0.01828', '0.06384', '0.1467', '-0.3984', '0.6104', '-0.1807', '0.2408', '0.834', '-0.4226', '-0.3325', '0.04553', '0.005173', '-0.4194', '0.2102', '0.11945', '-0.0377', '-0.1974', '0.729', '0.03256', '0.0668', '0.2036', '0.1539', '0.0734', '0.6973', '0.836', '0.1136', '0.2234', '0.4253', '0.1503', '-0.444', '-0.54', '0.3708', '0.422', '0.4558', '0.2406', '0.1156', '0.367', '0.00921', '0.335', '0.2893', '0.1761', '0.2374', '0.4858', '0.7515', '-0.315', '-0.10626', '0.682', '-0.0723']",C103968,0007459,,277.89,,,
mondo:0019170,polyarteritis nodosa,"['PAN', 'Küssmaul-Maier disease', 'polyarteritis nodosa', 'polyarteritis', 'periarteritis', 'periarteritis nodosa', 'classical polyarteritis nodosa', 'panarteritis nodosa', 'classic polyarteritis nodosa']",9810,,767,C0031036,,C26847,,D010488,446.0,M30.0,10036024,
mondo:0019171,familial long QT syndrome,"['Romano-Ward syndrome', 'hereditary long QT syndrome', 'Ward-Romano syndrome', 'Romano-Ward long QT syndrome', 'LQTS', 'congenital long QT syndrome']",,,768,C1141890,"['0.2632', '0.0847', '-0.75', '0.3008', '-0.3904', '-0.2803', '0.6924', '1.245', '-0.006893', '-0.1936', '0.532', '0.1707', '0.3093', '0.9126', '-0.3948', '0.1214', '-0.8438', '-0.1248', '0.08734', '-0.3804', '0.1461', '0.646', '0.1047', '0.1924', '0.4568', '-0.836', '0.2465', '0.2527', '0.7793', '-0.2318', '0.396', '0.3752', '0.3599', '0.2052', '-0.785', '-0.1987', '0.01897', '0.4365', '0.01967', '-0.336', '0.605', '-0.346', '0.0908', '-0.06647', '0.2788', '-0.5977', '-1.147', '0.01369', '0.0878', '0.28', '0.2191', '-0.4365', '-0.0945', '-0.0986', '-0.2169', '0.4912', '0.13', '0.3394', '-0.4473', '0.06006', '-0.3655', '0.486', '0.2847', '-0.392', '-0.7544', '0.4011', '0.1335', '-0.001868', '-0.4478', '0.7207', '-0.339', '0.733', '0.755', '-0.2062', '-0.2485', '0.6685', '0.08746', '-0.05142', '-0.3284', '0.357', '0.4973', '0.156', '0.1078', '-0.193', '0.5137', '-0.081', '0.4814', '-0.1979', '0.4495', '0.703', '0.1084', '0.1384', '0.0997', '-0.1589', '0.4917', '0.8267', '1.161', '-0.883', '-0.51', '-0.06183']",,,,,,10057926,
mondo:0019172,aniridia,['aplasia of iris'],12271,,77,C0003076,,C84563,,D015783,743.45,,10002532,
mondo:0019173,rabies,['lyssa'],11260,,770,C0034494,,C28182,,D011818,071,A82,10037742,
mondo:0019175,primary lymphedema,"['primary lymphedema', 'Troncular lymphatic malformation']",,,77240,,,C48829,,,,,,
mondo:0019176,trichorhinophalangeal syndrome type I or III,['trichorhinophalangeal syndrome type 1 and 3'],,,77258,CN205736,"['0.00314', '0.2289', '0.487', '-0.3186', '0.3652', '-0.1516', '0.1581', '0.3875', '-0.556', '-0.2673', '-0.0667', '0.0989', '-0.03726', '0.02756', '-0.2421', '0.0713', '0.5444', '-0.171', '0.08636', '-0.3672', '-0.0796', '0.3232', '0.794', '-0.2744', '0.3813', '0.1236', '-0.06134', '-0.144', '0.1655', '-0.1348', '0.4785', '-0.0757', '-0.1433', '0.1814', '0.5205', '-0.1904', '-0.2007', '-0.1852', '-0.2588', '-0.2937', '0.2625', '-0.4534', '-0.1676', '0.0377', '-0.02979', '-0.3213', '0.1577', '0.8086', '0.2288', '-0.2534', '-0.1935', '-0.1296', '-0.04022', '0.08105', '-0.4546', '-0.469', '-0.2551', '-0.312', '-0.02872', '0.09827', '0.01973', '0.0482', '-0.391', '0.1576', '0.02783', '-0.0197', '0.1159', '0.1285', '0.04153', '0.579', '-0.2134', '0.08075', '0.2942', '-0.252', '-0.1805', '0.1647', '-0.1522', '-0.3418', '-0.458', '-0.4436', '0.01566', '-0.08105', '-0.05182', '0.2917', '-0.1926', '-0.3533', '-0.1567', '0.521', '0.4092', '0.1892', '-0.1954', '0.3577', '0.3972', '0.2133', '0.526', '0.002052', '0.318', '-0.508', '0.1832', '0.12317']",,,,,,,
mondo:0019177,odontoleukodystrophy,"['dentoleukoencephalopathy', 'leukodystrophy with oligodontia']",,,77295,,,,,,,,,
mondo:0019178,auricular abnormalities-cleft lip with or without cleft palate-ocular abnormalities syndrome,,,,77300,CN205748,,,,,,,,
mondo:0019179,monosomy 9q22.3,['microdeletion 9q22.3'],,,77301,C3711390,,,,C579873,,,,
mondo:0019180,hereditary hemorrhagic telangiectasia,"['telangiectasia, hereditary Hemorrahagic, of Rendu, Osler', 'Rendu-Osler disease', 'Rendu-Osler-Weber disease', 'HHT', 'Osler-Weber-Rendu disease', 'telangiectasia, hereditary hemorrhagic', 'Osler hemorrhagic telangiectasia syndrome']",1270,,774,C0039445,"['0.08954', '0.4192', '-0.1757', '-0.1613', '-0.3586', '-0.1648', '0.0431', '0.4885', '-0.5464', '0.1285', '-0.509', '0.379', '0.1721', '0.3936', '-0.2253', '-0.13', '-0.12476', '-0.374', '-0.4177', '-0.3567', '-0.1526', '-0.3079', '0.5083', '0.4553', '-0.2343', '0.1298', '-0.1202', '0.1664', '0.5913', '-0.5864', '0.4155', '-0.512', '0.431', '0.0467', '0.4993', '0.331', '0.1582', '0.1986', '-0.519', '0.0428', '0.611', '-0.3289', '0.824', '-0.0894', '-0.000678', '-0.3462', '-0.7144', '-0.6475', '0.21', '-0.3088', '0.0942', '0.4597', '0.518', '0.664', '-0.2686', '-0.391', '0.1322', '1.253', '-0.1852', '-0.1586', '-0.3203', '0.0746', '0.4836', '-0.702', '0.616', '0.3652', '0.5005', '0.10376', '-0.3896', '0.8594', '0.4087', '0.0396', '0.1674', '0.2642', '0.4067', '-0.4138', '0.678', '-0.2201', '0.3464', '-0.0693', '-0.4856', '-0.603', '-0.0258', '0.02412', '0.4612', '0.2979', '0.645', '0.5283', '-0.2416', '-0.5767', '-0.10205', '-0.1087', '-0.3574', '-0.3523', '0.745', '-0.0976', '0.519', '-0.906', '0.504', '0.6274']",C35064,,D013683,448.0,I78.0,10019883,
mondo:0019181,non-syndromic X-linked intellectual disability,"['nonsyndromic X-linked intellectual disability', 'intellectual disability, X-linked, nonsyndromic', 'non-specific X-linked intellectual disability', 'isolated X-linked intellectual disability', 'X-linked non-syndromic intellectual disability', 'mental retardation, X-linked, nonsyndromic', 'non-syndromic intellectual disability, X-linked', 'non-specific X-linked mental retardation', 'X-linked non-specific intellectual disability', 'intellectual disability, nonsyndromic, X-linked', 'mental retardation, nonsyndromic, X-linked']",0050776,,777,C3501611,"['-0.11505', '0.1522', '0.1182', '-0.273', '0.0411', '-0.2966', '-0.07336', '0.01837', '-0.4368', '-0.375', '-0.03418', '-0.1471', '0.11743', '0.000492', '0.2377', '-0.0327', '-0.03192', '-0.05817', '-0.412', '-0.465', '0.00861', '0.1456', '0.337', '-0.1023', '0.2603', '-0.1348', '-0.0947', '-0.11914', '0.10474', '-0.1821', '0.285', '0.11664', '0.4448', '0.2009', '0.04953', '-0.2185', '-0.04846', '-0.3835', '-0.1803', '-0.1836', '0.46', '-0.338', '0.0123', '-0.01409', '0.1003', '-0.5005', '0.02773', '-0.2439', '0.2208', '0.08936', '-0.1466', '0.0514', '-0.2913', '-0.2023', '0.2435', '0.06287', '0.4714', '-0.232', '-0.1725', '0.3672', '-0.1343', '0.008415', '0.2766', '0.1628', '0.2239', '0.275', '-0.07825', '0.1837', '-0.283', '0.1525', '-0.5054', '-0.1326', '-0.1003', '-0.116', '0.2151', '0.1671', '0.3916', '-0.069', '-0.336', '-0.01904', '0.0959', '-0.03534', '-0.1014', '0.3293', '0.0802', '0.1852', '-0.02959', '0.168', '0.3357', '0.4338', '0.0954', '0.3289', '0.0558', '-0.401', '0.5146', '0.1318', '0.076', '-0.321', '0.326', '0.1335']",,,C564490,,,,
mondo:0019182,inherited obesity,"['obesity, association with, Autosomal recessive', 'obesity, mild, early-onset, Autosomal recessive', 'obesity, severe, Autosomal recessive', 'obesity, late-onset, Autosomal recessive', 'obesity, susceptibility to, Autosomal recessive', 'obesity, severe, and type II diabetes, Autosomal recessive', 'genetic obesity (disease)', 'obesity, early-onset, susceptibility to, Autosomal recessive', 'leanness, inherited, autosomal recessive']",,601665,77828,,"['-0.353', '0.4612', '-0.2133', '0.7905', '-0.2734', '-0.854', '0.2861', '0.6265', '-0.1508', '-0.634', '-0.11633', '0.3704', '0.2522', '0.409', '-0.7397', '-0.5127', '-0.2976', '0.843', '-0.7812', '-0.7246', '-0.03888', '-0.353', '0.295', '-0.273', '0.2754', '0.0993', '-0.3962', '-0.376', '0.2073', '-0.2847', '0.4146', '-0.796', '0.5312', '0.001062', '-0.3545', '-0.55', '-0.7275', '0.3762', '0.53', '-0.1593', '0.0793', '-0.1405', '-0.7603', '0.592', '0.12427', '-0.76', '0.583', '0.10406', '0.581', '0.1381', '-0.4636', '0.0789', '0.4207', '-0.3425', '-0.2954', '0.6416', '-0.192', '-0.0649', '-0.12494', '-0.663', '0.575', '0.3564', '-0.06464', '-0.7573', '-0.241', '0.785', '-0.3923', '0.3586', '0.4177', '0.5117', '0.349', '0.585', '-0.003033', '-0.2776', '0.65', '-0.562', '-0.329', '-0.11847', '-1.513', '0.2239', '-0.05594', '1.039', '-0.2428', '0.1481', '0.983', '0.6597', '0.1862', '0.299', '0.9766', '0.366', '-0.2301', '0.2837', '-0.1863', '0.692', '0.6206', '0.2441', '0.004833', '-0.4094', '-0.4968', '-0.0654']",,,,,,,
mondo:0019186,Q fever,"['query fever', 'quadrilateral fever', 'Q fever pneumonia', 'nine Mile fever', 'infection due to Coxiella burnetii', 'Coxiella burnetii fever', 'Coxiella burnetii caused disease or disorder', 'Coxiellosis']",11100,,781,C0034362,,C34970,0005224,D011778,083.0,A78,10037731,
mondo:0019187,Axenfeld-Rieger syndrome,"['Hagedoom syndrome', 'anomaly, Rieger^s', 'Rieger syndrome', 'iridogoniodysgenesis with somatic anomalies', 'Rieger^s anomaly', 'goniodysgenesis hypodontia', 'RGS - Rieger syndrome', 'Axenfeldt-Rieger syndrome', 'Axenfeld syndrome']",14686,,782,CN776842,"['-0.0569', '0.1908', '-0.2017', '-0.2128', '-0.313', '0.609', '0.0635', '0.57', '-0.4272', '-0.2474', '0.2184', '0.02301', '0.0701', '0.598', '-0.585', '-0.2837', '-0.1505', '-0.368', '0.10736', '-0.8457', '0.05148', '-0.0739', '0.657', '0.492', '-0.3499', '-0.0431', '-0.3513', '0.4375', '0.556', '-0.2551', '0.1572', '-0.1398', '-0.11566', '0.5425', '-0.2537', '0.3894', '0.3372', '-0.3855', '0.2766', '-0.643', '0.538', '0.2903', '0.3179', '0.1026', '0.4346', '0.2211', '0.566', '0.2773', '-0.2869', '-0.2507', '0.04858', '-0.0688', '-0.1395', '-0.511', '0.004654', '0.01097', '0.4338', '0.5195', '-0.659', '0.373', '0.4583', '0.274', '-0.0238', '0.5044', '0.06616', '-0.2383', '0.736', '0.2742', '-0.2074', '0.3716', '-0.537', '0.3345', '0.6387', '0.13', '-0.1367', '0.0858', '0.5864', '-0.431', '0.184', '-0.525', '0.1862', '-0.07355', '-0.3813', '0.8022', '-0.5693', '0.3274', '-0.1561', '-0.1019', '0.5103', '0.43', '0.0884', '0.3306', '0.232', '0.1974', '0.7915', '-0.8125', '0.553', '0.2676', '-0.02812', '-0.09485']",C131001,,C535679,743.44,,10059255,
mondo:0019188,Rubinstein-Taybi syndrome,"['Rubinstein syndrome', 'proximal chromosome 16p13.3 deletion syndrome', 'Broad thumb-hallux syndrome', 'Broad thumbs-halluces syndrome', 'Rubinstein-Taybi Syndrome', 'RSTS']",1933,,783,C0035934,"['0.4575', '-0.10223', '0.3594', '-0.534', '0.748', '-0.1459', '0.794', '0.973', '-0.4468', '-0.174', '0.2302', '0.1862', '0.00726', '-0.3352', '-0.461', '0.154', '-0.1548', '0.1389', '-0.569', '-0.3682', '-0.0638', '0.515', '0.04053', '0.2006', '0.2825', '-0.2462', '-0.01552', '0.8765', '0.408', '-0.556', '0.675', '0.01039', '0.769', '0.1577', '-0.542', '0.1267', '0.3472', '0.09296', '-0.0793', '-0.1506', '0.5576', '0.1304', '0.2316', '-0.10913', '-0.0514', '-0.4375', '0.01797', '0.6616', '-0.2167', '0.168', '-0.4495', '0.364', '-0.3945', '0.0809', '0.2181', '-0.5347', '-0.461', '-0.2188', '0.2678', '-0.339', '0.1146', '0.3015', '-0.03964', '0.3691', '0.2289', '0.1666', '0.527', '-0.2505', '-0.2249', '0.3772', '0.299', '0.4648', '-0.1492', '-0.4297', '0.4258', '-0.006027', '-0.139', '-0.2512', '-0.509', '0.0965', '0.2256', '-0.1716', '0.0589', '0.3088', '-0.1602', '-0.1207', '0.1333', '0.531', '0.193', '0.2886', '-0.5728', '0.1361', '-0.4858', '0.2034', '0.3252', '-0.5205', '0.476', '-0.1746', '0.0933', '0.2966']",C75466,,D012415,759.89,,10039281,
mondo:0019189,inborn disorder of amino acid and other organic acid metabolism,['disorder of amino acid and other organic acid metabolism'],,,79062,C0342666,,,,,270.8,,,
mondo:0019190,juvenile polyposis of infancy,"['infantile onset juvenile polyposis syndrome', 'infantile juvenile polyposis syndrome', 'juvenile polyposis syndrome of infancy']",,,79076,CN205768,,,,,,,,
mondo:0019191,IgG4-related dacryoadenitis and sialadenitis,"['Mikulicz disease', 'Mikulicz syndrome (former)', 'chronic dacryoadenitis and sialadenitis', 'Mikulicz^s disease', 'Mikulicz^s disease (former)', 'Mikulicz disease (former)']",12900,,79078,C0026103,,C34819,,D008882,,,10052317,
mondo:0019192,AKT2-related familial partial lipodystrophy,"['familial partial lipodystrophy due to AKT2 mutations', 'AKT2-related FPLD']",,,79085,CN536246,,,,,,,,
mondo:0019193,acquired generalized lipodystrophy,"['acquired generalized lipodystrophy', 'Lawrence syndrome', 'acquired lipoatrophic diabetes', 'Lawrence-Seip syndrome']",0080300,,79086,C0271693,,C131089,,,,,,
mondo:0019194,localized lipodystrophy,"['focal lipodystrophy', 'panniculitis and localised lipodystrophy (subtype)', 'drug-induced localised lipodystrophy (subtype)', 'drug-induced localized lipodystrophy (subtype)', 'idiopathic localized lipodystrophy (subtype)', 'pressure-induced localized lipoatrophy (subtype)', 'idiopathic localised lipodystrophy (subtype)', 'pressure-induced localised lipoatrophy (subtype)', 'panniculitis and localized lipodystrophy (subtype)', 'centrifugal lipodystrophy (subtype)']",,,79088,CN227583,,C131814,,,,,,
mondo:0019195,hereditary inclusion body myopathy-joint contractures-ophthalmoplegia syndrome,"['HIBM3', 'hereditary inclusion body myopathy type 3', 'inclusion body myopathy type 3', 'IBM3', 'Myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles', 'Inclusion body myopathy autosomal dominant', 'Hereditary inclusion body myopathy type 3', 'Hereditary inclusion body myopathy - joint contractures - ophthalmoplegia']",,,79091,CN205775,"['-0.5186', '-0.04565', '-0.578', '-0.4023', '0.3462', '-0.989', '-0.005024', '0.3955', '-0.816', '0.2384', '-0.398', '0.03894', '0.2693', '0.1605', '0.4526', '0.1975', '-0.11127', '0.1251', '-0.5825', '-0.5444', '0.01472', '-0.3445', '0.3003', '0.1776', '-0.01455', '-0.2', '-0.1877', '-0.1049', '-0.1858', '-0.3093', '0.7554', '-0.1131', '0.4343', '-0.1455', '0.04678', '-0.6313', '-0.3774', '-0.2585', '0.1566', '-0.2191', '0.01059', '-0.4812', '-0.4666', '0.516', '-0.4277', '0.005074', '-0.1936', '-0.1552', '-0.05', '-0.0311', '-0.2732', '0.0733', '0.1476', '0.0855', '-0.02274', '-0.5903', '0.582', '-0.08246', '0.10046', '-0.06094', '0.3071', '-0.2079', '0.02945', '-0.00961', '-0.4697', '0.011375', '0.5874', '0.784', '-0.6694', '0.2023', '-0.03534', '-0.01354', '0.229', '0.1692', '0.1702', '-0.216', '-0.2004', '0.3496', '-0.479', '-0.1825', '0.1606', '0.286', '0.4011', '0.3877', '-0.2944', '0.3523', '-0.01743', '0.408', '-0.3506', '-0.1504', '0.4558', '0.363', '0.1113', '0.1266', '0.5303', '-0.07874', '0.745', '-0.0405', '-0.1665', '-0.1385']",,,,,,,
mondo:0019196,Foix-Alajouanine syndrome,"['Subacute necrotizing myelitis', 'angiodysgenetic necrotizing myelopathy', 'Subacute angiohypertrophic myelomalacia', 'familial osteosclerosis with abnormalities of the nervous system and meninges', 'Subacute ascending necrotizing myelitis']",,,79093,CN205776,,,,,323.9,,,
mondo:0019197,folinic acid-responsive seizures,['Folinic acid responsive seizures'],,,79097,CN205780,,,,,,,,
mondo:0019198,sympathetic ophthalmia,"['sympathetic uveitis', 'sympathetic ophthalmia']",12029,,79098,C0029077,,,1001205,D009879,360.11,,10042742,
mondo:0019199,interstitial granulomatous dermatitis with arthritis,"['Ackerman dermatitis syndrome', 'IGDA']",,,79099,CN205782,,,,,,,,
mondo:0019200,retinitis pigmentosa,"['Rod-cone dystrophy', 'pericentral pigmentary retinopathy']",10584,268000,791,C4072872,,C85045,,D012174,,H35.5,10038914,
mondo:0019201,thyrotoxic periodic paralysis,['thyrotoxic hypokalemic periodic paralysis'],,,79102,C0268446,"['-0.2272', '0.4148', '-0.9243', '-0.2474', '-0.279', '-0.618', '0.532', '0.4917', '-0.209', '0.4116', '-0.588', '0.3386', '-0.09686', '0.5156', '-0.11285', '0.4148', '-0.478', '-0.10596', '-0.2056', '-0.8213', '-0.04617', '0.2437', '0.901', '0.04633', '-0.4194', '-0.4438', '-0.1918', '0.00988', '-0.2625', '-0.2087', '0.415', '0.01435', '0.1777', '-0.08356', '-0.7495', '-0.158', '0.0213', '0.156', '-0.537', '0.395', '-0.2319', '-0.1648', '0.3635', '-0.04355', '0.4482', '0.3235', '-0.4246', '0.05554', '0.08344', '0.8726', '-0.5083', '0.2615', '0.3938', '-0.5483', '0.06042', '-0.1593', '0.539', '-0.744', '0.1179', '0.0839', '0.185', '0.508', '0.04538', '0.1488', '-0.5923', '0.353', '0.0698', '0.8247', '-0.4895', '0.3447', '-0.4895', '0.02689', '-0.1001', '-0.2129', '0.6553', '0.1676', '0.1687', '0.1559', '0.3025', '-0.2137', '0.212', '-0.3696', '-0.04898', '-0.03574', '0.1071', '0.11536', '0.0658', '0.8506', '-0.0761', '-0.348', '0.504', '-0.2163', '-0.0501', '-0.3362', '0.5327', '-0.3635', '0.241', '-0.6523', '-0.552', '-0.383']",,,,,,10043788,
mondo:0019202,myxofibrosarcoma,"['fibromyxosarcoma', 'MFS', 'myxofibrosarcoma', 'myxoid malignant fibrous histiocytoma', 'myxoid fibrous histiocytoma', 'myxoid MFH']",0080534,,79105,,,C6496,,,,,10066948,
mondo:0019203,acute interstitial pneumonia,"['acute interstitial pneumonitis', 'accelerated interstitial pneumonia', 'idiopathic pulmonary fibrosis, acute fatal form', 'Hamman-rich syndrome', 'AIP', 'Hamman-rich disease']",2800,,79126,C1279945,,C35806,,,516.33,,10066728,
mondo:0019204,respiratory bronchiolitis-interstitial lung disease syndrome,['RB-ILD'],,,79127,CN205794,,,,,,,10066393,
mondo:0019205,trichodysplasia-amelogenesis imperfecta syndrome,,,,79129,CN205796,,,,,,,,
mondo:0019206,sparse hair-short stature-skin anomalies syndrome,,,,79132,CN205797,,,,,,,,
mondo:0019207,DEND syndrome,"['developmental delay-epilepsy-neonatal diabetes syndrome', 'K ATP associated developmental delay, epilepsy and neonatal diabetes']",,,79134,C4303593,"['0.112', '0.4453', '0.0489', '-0.2466', '-0.05222', '-0.6665', '0.081', '0.5317', '-0.06323', '-0.575', '-0.752', '-0.3726', '0.01178', '-0.2128', '-0.0817', '-0.3489', '0.1339', '-0.01452', '0.2615', '-1.054', '0.3677', '-0.04294', '0.2299', '-0.2214', '-0.0427', '0.06964', '0.04086', '-0.071', '0.401', '-0.3406', '0.3967', '0.1428', '0.565', '0.3838', '-0.1846', '0.278', '-0.4885', '-0.52', '-0.5376', '0.2756', '-0.0806', '-0.4985', '0.3323', '0.03964', '-0.2947', '-0.1475', '-0.01018', '-0.005737', '-0.05658', '-0.1065', '0.0969', '0.4282', '-0.1333', '-0.1351', '0.10876', '0.000823', '0.0173', '-0.501', '0.04865', '0.483', '-0.1073', '-0.0874', '0.4788', '-0.431', '-0.1009', '0.2422', '0.01427', '0.455', '-1.23', '0.1671', '0.4624', '-0.0724', '0.25', '0.1134', '0.2438', '0.2507', '0.2289', '0.2517', '-0.2578', '0.1315', '0.2544', '0.1774', '-0.695', '-0.03', '0.1462', '0.61', '0.1273', '0.5474', '0.608', '0.3765', '0.942', '0.3816', '-0.01512', '0.002907', '0.402', '0.05945', '0.06235', '-0.6475', '0.2068', '0.1418']",C131845,,,,,,
mondo:0019208,Bickerstaff brainstem encephalitis,,,,79138,C1960543,,,,,323.81,,,
mondo:0019209,Japanese encephalitis,"['Japanese B encephalitis', 'JE']",10844,,79139,C0014057,,C34577,0007332,D004672,062.0,,10014596,
mondo:0019210,cutaneous neuroendocrine carcinoma,"['neuroendocrine carcinoma of skin', 'carcinoma, Merkel cell', 'cutaneous neuroendocrine carcinoma', 'trabecular skin carcinoma', 'Merkel cell tumor', 'MCC', 'Merkel cell cancer', 'neuroendocrine carcinoma of the skin', 'Merkle tumors', 'carcinoma of Merkel cell', 'Merkel cell carcinoma', 'Merkle tumours', 'trabecular cancer', 'cutaneous APUDoma', 'Merkel cell tumour', 'neuroendocrine skin carcinoma']",,,79140,C0007129,,C9231,1001471,D015266,209.36,,,
mondo:0019211,isolated congenital anonychia,"['isolated anonychia', 'autosomal recessive nonsyndromic congenital nail disorder-4', 'nonsyndromic congenital nail disorder, 4', 'congenital anonychia']",,,79143,,"['0.03366', '0.3665', '-0.01484', '-0.0362', '0.571', '-0.3271', '-0.3533', '0.2844', '0.1148', '-0.502', '-0.06555', '-0.0766', '-0.4246', '0.01872', '0.12115', '0.375', '0.2367', '-0.2607', '-0.2462', '-0.5244', '-0.4404', '0.1042', '0.4436', '-0.2104', '0.2927', '0.166', '-0.2037', '0.0262', '0.3289', '-0.4705', '0.3086', '-0.1952', '-0.1367', '0.0938', '-0.0605', '-0.2893', '-0.2057', '-0.3088', '0.03748', '-0.2556', '-0.201', '-0.3323', '0.0724', '-0.385', '0.02783', '-0.354', '-0.218', '0.321', '-0.2206', '-0.4128', '0.1573', '-0.3816', '0.02', '-0.12256', '-0.3438', '-0.3962', '0.6167', '0.07117', '-0.3604', '-0.1698', '0.0633', '0.00099', '0.136', '0.0916', '0.02977', '-0.04605', '0.1957', '0.3186', '-0.3423', '0.3318', '-0.151', '-0.0454', '-0.01656', '-0.1537', '0.2722', '0.2412', '0.0091', '-0.02625', '-0.0548', '-0.247', '0.1705', '0.4124', '0.4666', '0.03128', '0.07935', '0.2014', '-0.211', '0.729', '-0.129', '0.2532', '-0.179', '0.5527', '0.02974', '0.1406', '0.8086', '0.02623', '0.2822', '-0.678', '0.1508', '-0.10016']",,,,,,,
mondo:0019212,disseminated superficial actinic porokeratosis,,,,79152,,"['0.3855', '0.158', '-0.8633', '-0.299', '0.1816', '-0.4307', '0.2213', '-0.00575', '-0.343', '-0.375', '0.1682', '0.396', '0.0875', '0.629', '-0.3794', '-0.01497', '0.2996', '-0.826', '0.03818', '-0.3665', '-0.558', '-0.784', '0.743', '-0.2332', '-0.04727', '0.1714', '-0.739', '-0.3108', '-0.2485', '0.002628', '0.1697', '-0.3376', '0.0219', '-0.0651', '0.05884', '0.3723', '-0.3027', '-0.361', '0.04654', '0.3494', '0.4753', '-1.007', '0.5776', '-0.3667', '0.035', '0.0869', '-0.4502', '-0.196', '0.2925', '0.2952', '-0.03775', '-0.2361', '0.01331', '0.363', '-0.963', '0.293', '0.1416', '-0.004223', '-0.3608', '0.1505', '0.3552', '-0.04675', '-0.4526', '0.3323', '0.03207', '0.4998', '0.3', '0.6934', '0.634', '1.2', '0.4214', '-0.377', '0.4688', '0.2683', '0.2412', '0.2164', '-0.0983', '-0.327', '-0.5107', '-0.504', '0.02516', '-0.532', '-0.3672', '0.1252', '-0.258', '-0.483', '-0.3743', '0.05048', '0.6694', '0.2637', '0.245', '0.2974', '-0.02998', '0.2053', '0.0618', '-0.2283', '0.2634', '-1.106', '-0.1686', '-0.482']",,,,692.75,,,
mondo:0019213,cerebral organic aciduria,"['brain inherited organic acidemia', 'inherited organic acidemia of brain']",,,79158,,,,,,,,,
mondo:0019214,inborn carbohydrate metabolic disorder,"['disorder of carbohydrate transport and metabolism', 'rare inborn error of carbohydrate metabolic process', 'disorder of carbohydrate metabolism', 'inborn errors of carbohydrate metabolism', 'inborn error of carbohydrate metabolic process', 'carbohydrate metabolic disorder', 'inborn carbohydrate metabolism disorder', 'carbohydrate metabolism disorder']",2978,,79161,,,C97089,1000061,D002239,271.8,,10061023,
mondo:0019215,classic organic aciduria,,,,79163,,,,,,,,,
mondo:0019216,inborn disorder of amino acid transport,['disorder of amino acid absorption and transport'],,,79166,C0268641,,,,,270.0,,,
mondo:0019218,inborn disorder of bile acid synthesis,"['inborn error of bile acid biosynthetic process', 'rare inborn error of bile acid biosynthetic process', 'inborn errors of bile acid synthesis', 'disorder of bile acid synthesis']",,,79168,CN544763,"['-0.3877', '0.07086', '-0.1703', '0.1471', '0.2612', '-0.3472', '-0.07', '0.672', '0.1296', '0.3809', '-0.2761', '-0.711', '-0.1792', '0.5444', '-0.718', '-0.2803', '0.3052', '-0.359', '-0.5107', '-0.668', '-0.3982', '-0.894', '0.5776', '-0.424', '-0.505', '-0.758', '-0.0844', '-0.264', '-0.0846', '0.4421', '0.647', '0.2085', '0.26', '0.8286', '-0.1927', '-0.03452', '-0.2336', '-0.03111', '-0.037', '0.727', '0.2605', '-0.3584', '0.0801', '0.1355', '-0.4805', '-0.4622', '0.9307', '-0.5967', '0.09546', '-0.00615', '-0.0768', '0.02939', '0.0904', '-0.2245', '-0.3845', '-0.4832', '0.09326', '0.2832', '-0.565', '0.1946', '0.781', '0.275', '0.53', '-0.3538', '0.5854', '0.2883', '0.1528', '-0.1393', '-0.2888', '0.1279', '-0.26', '0.2219', '-0.1835', '-0.34', '1.134', '0.1411', '-0.0006847', '-0.7896', '-0.1946', '-0.1454', '-0.0842', '-0.2776', '-0.5825', '-0.2122', '-0.0548', '-0.2041', '-0.00648', '0.1577', '0.4302', '-0.1764', '0.7446', '0.3794', '-0.3914', '-0.4905', '0.4082', '0.589', '0.4978', '-0.3828', '0.1646', '0.1521']",,,,,,,
mondo:0019219,inborn disorder of neurotransmitter metabolism and transport,['disorder of neurotransmitter metabolism and transport'],,,79169,CN227586,,,,,,,,
mondo:0019220,inborn disorder of cobalamin metabolism and transport,['disorder of cobalamin metabolism and transport'],,,79171,CN227587,,,,,,,,
mondo:0019222,inborn disorder of methionine cycle and sulfur amino acid metabolism,"['inborn error of sulphur amino acid metabolic process', 'cytosolic methyl group transfer or sulfur amino acid metabolism disorder', 'rare inborn error of sulfur amino acid metabolic process', 'disorder of methionine cycle and sulfur amino acid metabolism', 'disorder of methionine cycle and sulphur amino acid metabolism', 'rare inborn error of sulphur amino acid metabolic process', 'inborn sulphur amino acid metabolic process disorder', 'inborn error of sulfur amino acid metabolic process', 'cytosolic methyl group transfer or sulphur amino acid metabolism disorder']",,,79173,CN227589,,,,,270.4,,,
mondo:0019223,disorder of fatty acid and ketone body metabolism,"['inborn disorder of fatty acid oxidation and ketone body metabolism', 'disorder of fatty acid oxidation and ketone body metabolism']",,,79174,CN227590,,,,,,,,
mondo:0019224,inborn disorder of gamma-aminobutyric acid metabolism,"['inborn error of gamma-aminobutyric acid metabolic process', 'disorder of GABA metabolism', 'rare inborn error of gamma-aminobutyric acid metabolic process', 'disorder of gamma-aminobutyric acid metabolism']",,,79175,CN227591,,,,,,,,
mondo:0019225,disorder of gluconeogenesis,"['gluconeogenesis disorder', 'inborn error of gluconeogenesis', 'rare inborn error of gluconeogenesis']",,,79177,CN227592,,,,,,,,
mondo:0019226,glucose transport disorder,"['rare inborn error of glucose transport', 'inborn error of glucose transport']",,,79178,CN227593,,,,,,,,
mondo:0019227,inborn disorder of glycerol metabolism,"['inborn error of glycerol metabolic process', 'disorder of glycerol metabolism', 'rare inborn error of glycerol metabolic process']",,,79179,C0342762,,,,,,,,
mondo:0019228,inborn disorder of histidine metabolism,"['histidine metabolic process disease', 'disorder of histidine metabolic process', 'inborn error of histidine metabolic process', 'inborn error of histidine metabolism', 'disturbance of histidine metabolism', 'inborn disorder of histidine metabolism', 'rare inborn error of histidine metabolic process', 'disorder of histidine metabolism', 'histidine metabolism disease']",9265,,79181,C0268512,,,,,270.5,E70.40,,
mondo:0019229,inborn disorder of ketolysis,"['disorder of ketolysis', 'inborn error of ketone body catabolic process', 'rare inborn error of ketone body catabolic process']",,,79183,CN227594,,,,,,,,
mondo:0019230,inborn disorder of ornithine or proline metabolism,['disorder of ornithine or proline metabolism'],,,79185,CN227595,,,,,,,,
mondo:0019231,inborn disorder of pentose phosphate metabolism,['disorder of pentose phosphate metabolism'],,,79186,CN227596,,,,,,,,
mondo:0019232,inborn disorder of peptide metabolism,['disorder of peptide metabolism'],,,79187,CN227597,,,,,,,,
mondo:0019233,disorder of peroxisomal beta oxidation,['disorder of peroxisomal beta oxidation'],,,79188,CN227598,,,,,,,,
mondo:0019234,peroxisome biogenesis disorder,"['Zellweger spectrum disorder', 'peroxisomal biogenesis disorders, Zellweger syndrome spectrum', 'PBD, ZSS', 'peroxisome biogenesis disorders, Zellweger syndrome spectrum', 'disorders of peroxisome biogenesis', 'PBD-ZSD', 'peroxisomal biogenesis disorders', 'Zellweger spectrum', 'peroxisome biogenesis disorder', 'peroxisome biogenesis disorder-Zellweger syndrome spectrum', 'Zellweger spectrum disorders', 'peroxisome biogenesis disorder spectrum', 'ZSD', 'PBD-ZSS', 'cerebrohepatorenal syndrome', 'Zellweger syndrome spectrum', 'PBD-Zellweger spectrum disorder']",0080377,,79189,,,C155747,,C536664,,,,
mondo:0019235,inborn disorder of phenylalanine and tyrosine metabolism,"['inborn disorder of phenylalanin or tyrosine metabolism', 'disorder of phenylalanin or tyrosine metabolism']",,,79190,CN227599,,,,,,,,
mondo:0019236,inborn disorder of purine metabolism,"['rare inborn error of purine nucleobase metabolic process', 'disorder of purine metabolism', 'inborn error of purine nucleobase metabolic process']",,,79191,C0268104,,,,,,,10061476,
mondo:0019237,inborn disorder of pyridoxine metabolism,"['disorder of pyridoxine metabolism', 'rare inborn error of pyridoxine metabolic process', 'inborn error of pyridoxine metabolic process']",,,79192,CN227600,,,,,,,,
mondo:0019238,inborn disorder of pyrimidine metabolism,"['disorder of pyrimidine metabolism', 'pyrimidine metabolic disorder', 'rare inborn error of pyrimidine nucleobase metabolic process', 'inborn error of pyrimidine nucleobase metabolic process']",0050832,,79193,C0268127,,,,,,,10070969,
mondo:0019239,inborn disorder of serine family metabolism,"['disorder of serine or glycine metabolism', 'inborn error of serine family amino acid metabolic process', 'rare inborn error of serine family amino acid metabolic process', 'inborn disorder of serine or glycine metabolism']",,,79194,CN227601,,,,,,,,
mondo:0019240,sterol biosynthesis disorder,"['inborn error of sterol biosynthetic process', 'rare inborn error of sterol biosynthetic process']",,,79195,CN227602,,,,,,,,
mondo:0019241,inborn disorder of the gamma-glutamyl cycle,['disorder of the gamma-glutamyl cycle'],,,79196,C0268517,,,,,,,,
mondo:0019242,inborn disorder of branched-chain amino acid metabolism,"['disorder of branched-chain amino acid metabolism', 'rare inborn error of branched-chain amino acid metabolic process', 'inborn disorder of branched-chain amino acid metabolism', 'inborn error of branched-chain amino acid metabolic process']",,,79197,C0342712,,,,,,,,
mondo:0019243,inborn disorder of energy metabolism,"['disorder of energy metabolism', 'inborn error of generation of precursor metabolites and energy', 'rare inborn error of generation of precursor metabolites and energy']",,,79200,CN227604,,,,,,,,
mondo:0019245,lysosomal lipid storage disorder,"['lipoidosis', 'lipoid storage diseas', 'inborn lipid storage disorder', 'inborn error of lipid storage', 'lipid storage disease', 'rare inborn error of lipid storage']",9455,,79204,CN205834,,,,D008064,272.8,,,
mondo:0019246,inborn disorder of lysosomal amino acid transport,['disorder of lysosomal amino acid transport'],,,79207,CN227605,,,,,,,,
mondo:0019248,mucolipidosis,,0080488,,79212,C0026697,,C61267,,D009081,,,,
mondo:0019249,mucopolysaccharidosis,"['mucopolysaccharidosis', 'MPS', 'mucopolysaccharidoses']",12798,,79213,C0026703,,C61259,,D009083,277.5,,10028093,
mondo:0019250,inborn disorder of biogenic amine metabolism and transport,['disorder of biogenic amine metabolism and transport'],,,79214,CN227606,,,,,,,,
mondo:0019251,oligosaccharidosis,,,,79215,,,,,,,,,
mondo:0019253,metabolic disease involving other neurotransmitter deficiency,,,,79219,CN205839,,,,,,,,
mondo:0019254,inborn disorder of purine or pyrimidine metabolism,"['inborn purine-pyrimidine metabolic disorder', 'purine-pyrimidine metabolic disorder', 'disorder of purine or pyrimidine metabolism', 'inborn errors of purine-pyrimidine metabolism']",653,,79224,C0034139,,,,D011686,277.2,,10037546,
mondo:0019255,sphingolipidosis,['sphingolipidoses'],1927,,79225,C0037899,,C117254,,D013106,,,,
mondo:0019256,sterol metabolism disorder,"['rare inborn error of sterol metabolic process', 'inborn error of sterol metabolic process']",,,79226,CN227607,,,,,,,,
mondo:0019257,hemochromatosis type 2,"['juvenile hemochromatosis', 'JHH', 'hemochromatosis juvenile', 'HFE2', 'iron overload disease juvenile']",0111034,,79230,CN205842,"['0.2532', '0.3132', '-0.258', '0.1844', '0.646', '-0.2445', '-0.714', '0.489', '0.02864', '0.04932', '0.02698', '0.4312', '-0.4456', '0.6865', '-0.578', '-0.0615', '-0.6196', '0.1575', '-0.4995', '-0.925', '-0.5166', '-0.4958', '0.2307', '-0.4456', '0.3123', '0.1158', '0.2168', '-0.1257', '0.218', '0.0458', '1.03', '-0.619', '0.6465', '0.0693', '-0.005974', '-0.4053', '-1.016', '-0.2598', '0.1313', '0.1249', '0.2441', '-0.1302', '-0.0812', '0.5205', '0.2595', '-0.916', '0.1461', '-0.4543', '-0.10626', '-0.1533', '0.205', '-0.0487', '0.6187', '0.2247', '0.525', '-0.3445', '0.1494', '0.4807', '-0.262', '-0.04514', '0.588', '0.793', '0.7334', '-0.03885', '-0.10095', '0.04532', '-0.1989', '0.3958', '-0.803', '-0.4666', '0.2598', '0.1835', '0.1378', '-0.3445', '0.3142', '-0.249', '-0.1437', '0.963', '-0.264', '0.5996', '0.11926', '-0.5244', '-0.1324', '-0.4558', '-0.1877', '-0.5425', '0.8687', '0.4622', '0.6553', '-0.08606', '1.074', '0.262', '-0.3672', '-0.3955', '0.73', '0.822', '-0.02338', '-0.2654', '-0.3875', '-0.01596']",,,C537247,,,,
mondo:0019258,mild phenylketonuria,"['mild PKU', 'variant phenylketonuria', 'variant PKU', 'mPKU']",,,79253,,,,,,,,,
mondo:0019259,classic phenylketonuria,['classic PKU'],,,79254,C0751434,,,,,,,10034875,
mondo:0019260,adult neuronal ceroid lipofuscinosis,"['adult NCL', 'Kufs disease', 'ANCL', 'CLN4 disease, adult autosomal dominant', 'Kuf^s disease', 'neuronal ceroid lipofuscinosis 4', 'neuronal ceroid lipofuscinosis of adults']",,,79262,CN205864,"['0.0476', '0.641', '-0.1106', '0.1221', '-0.0325', '-0.75', '0.2032', '0.3105', '-0.6074', '-0.0334', '-0.644', '0.00793', '0.2323', '0.05563', '0.3584', '-0.4717', '-0.05127', '-0.3252', '-0.2448', '-0.652', '0.04086', '-0.3545', '0.0718', '0.06216', '0.1359', '0.1644', '-0.2566', '-0.2686', '-0.6377', '0.755', '0.529', '-0.289', '0.07666', '0.035', '0.2852', '0.4558', '-0.05957', '-0.373', '-0.7085', '-0.2358', '0.10913', '-0.406', '0.4075', '-0.0603', '0.2073', '-0.5073', '-0.2238', '0.077', '0.4058', '0.7075', '0.511', '0.5205', '-0.4346', '-0.3198', '0.6177', '-0.6973', '0.5806', '-0.3796', '-0.7656', '0.2317', '-0.003403', '-0.1403', '0.445', '-0.0824', '-0.1871', '0.4878', '0.5933', '0.3997', '-0.2878', '0.4492', '-0.0858', '-0.0888', '0.12305', '0.06165', '0.6943', '-0.0739', '0.3455', '0.2118', '-0.4592', '-0.379', '0.4243', '-0.3198', '-0.11475', '0.722', '0.1309', '-0.581', '0.05402', '0.155', '0.2007', '0.0907', '0.535', '0.08844', '-0.2133', '-0.011696', '-0.1356', '0.342', '0.967', '-0.0652', '0.3179', '0.186']",,,,,,,
mondo:0019261,infantile neuronal ceroid lipofuscinosis,"['Santavuori-Haltia disease', 'Hagberg-Santavuori disease', 'Santavuori disease', 'INCL', 'infantile NCL']",,,79263,,"['0.2145', '0.4321', '-0.02682', '0.0663', '0.001494', '-0.878', '-0.2256', '1.008', '-0.548', '0.1279', '-0.6855', '0.001995', '0.191', '-0.03061', '0.04056', '-0.4773', '-0.0882', '-0.409', '-0.0645', '-0.1473', '0.1664', '-0.608', '-0.1255', '-0.291', '-0.2937', '-0.2217', '-0.5493', '-0.02432', '-1.195', '0.3723', '0.8174', '0.03387', '0.2241', '-0.7104', '0.2279', '0.2725', '-0.782', '0.3186', '-0.5005', '0.2966', '-0.33', '0.103', '0.5215', '-0.1147', '0.2961', '-0.4663', '-0.3696', '-0.1313', '-0.0922', '0.323', '0.669', '0.2246', '-0.8745', '-0.1764', '0.5723', '-1.17', '1.034', '-0.2157', '-0.392', '0.314', '-0.0576', '0.2231', '0.1694', '-0.05844', '0.4695', '-0.2766', '1.014', '-0.11755', '-0.2227', '0.1509', '-0.3506', '-0.01952', '-0.2355', '-0.6416', '0.2769', '0.4734', '0.0223', '0.003622', '-1.056', '0.04102', '0.849', '0.3613', '-0.5894', '0.554', '0.3018', '-0.6143', '0.315', '0.8154', '-0.1143', '0.2744', '0.06207', '0.07025', '-0.3235', '0.2754', '0.08014', '0.2446', '0.5923', '-0.5605', '0.8467', '-0.08496']",,,,,,,
mondo:0019262,juvenile neuronal ceroid lipofuscinosis,"['juvenile neuronal ceroid lipofuscinosis', 'juvenile NCL', 'JNCL', 'batten disease', 'Spielmeyer-Vogt disease']",0050756,,79264,,"['0.639', '0.7007', '0.3323', '0.4475', '-0.085', '-0.8853', '-0.1992', '0.713', '-0.516', '-0.292', '-0.783', '-0.1957', '-0.1665', '0.05426', '0.5166', '-0.252', '-0.06116', '-0.0626', '-0.4277', '-0.652', '0.3362', '-0.2122', '0.3257', '-0.1571', '-0.2172', '-0.2317', '-0.599', '-0.4624', '-0.2015', '0.1246', '0.4404', '-0.3083', '0.05508', '-0.0698', '0.2605', '-0.001173', '0.3193', '-0.6626', '-0.4797', '0.04047', '0.554', '-0.798', '0.2693', '-0.3738', '0.351', '0.0554', '-0.4138', '-0.1224', '0.1493', '1.338', '0.4995', '0.6353', '-0.2883', '-0.771', '0.768', '-0.6333', '0.932', '-0.3293', '-0.1835', '0.1857', '-0.1661', '0.09503', '-0.03766', '-0.0783', '0.497', '0.568', '0.3342', '0.1646', '-0.415', '0.371', '0.2576', '0.01026', '0.2438', '-0.2123', '0.4114', '0.2203', '-0.114', '-0.0631', '-0.8457', '0.2705', '0.5938', '-0.3303', '-0.31', '0.591', '0.11676', '-0.6504', '0.412', '0.1716', '0.525', '0.00428', '0.8154', '0.1726', '0.0468', '0.0654', '0.193', '-0.10846', '0.3435', '-0.133', '0.317', '-0.0316']",,,,,,10052073,
mondo:0019263,autosomal erythropoietic protoporphyria,['EPP'],,,79278,,,,,,,,10015289,
mondo:0019264,alpha-N-acetylgalactosaminidase deficiency type 3,"['Schindler disease type 3', 'NAGA deficiency type 3']",0112320,,79281,C1836545,,,,,,,,
mondo:0019265,diazoxide-resistant focal hyperinsulinism,"['hyperinsulinemic hypoglycemia, diazoxide-resistant focal form']",,,79298,,,,,,,,,
mondo:0019266,SAPHO syndrome,"['acquired hyperostosis syndrome', 'synovitis, acne, Pustlosis, hyperostosis, and osteomyelitis', 'synovitis-acne-pustulosis-hyperostosis-osteitis syndrome', 'synovitis acne pustulosis hyperostosis osteitis', 'synovitis, acne, pustulosis palmaris, hyperostosis, osteomyelitis syndrome', 'synovitis, acne, pustulosis, hyperostosis, and osteitis syndrome', 'Pustulo-psoriatic hyperostotic Spondyloarthritis', 'PPHS']",13677,,793,C0263859,,C119049,1001164,D020083,706.1,,10051316,
mondo:0019267,vitamin B12-unresponsive methylmalonic acidemia type mut-,"['partial deficiency of methylmalonyl-CoA mutase', 'vitamin B12-unresponsive methylmalonic aciduria type mut-']",,,79312,CN205894,"['0.09326', '-0.00715', '-0.5537', '-0.2668', '0.11597', '-0.4683', '-0.02238', '0.289', '-0.0761', '-0.006073', '-0.4822', '-0.643', '-0.1854', '0.3862', '-0.582', '-0.443', '0.06104', '0.01135', '0.1013', '-0.9224', '0.01208', '-0.275', '0.404', '-0.3025', '0.188', '-0.2507', '0.2152', '-0.2917', '-0.01973', '0.0182', '0.1342', '-0.00011766', '0.5903', '0.2988', '-0.1716', '0.143', '-0.1735', '-0.5894', '-0.11926', '0.507', '0.04562', '-0.3306', '0.2996', '0.4075', '0.124', '-0.11206', '-0.11475', '-0.04877', '-0.6973', '0.2258', '-0.005993', '-0.00408', '0.02037', '-0.3943', '-0.2277', '0.03', '0.04782', '-0.1049', '-0.2566', '0.607', '-0.07135', '0.04123', '0.0734', '-0.2834', '0.06323', '-0.05823', '0.1672', '0.255', '-0.7812', '0.6143', '0.3809', '-0.03415', '0.007935', '-0.655', '0.16', '0.5635', '-0.00977', '-0.4949', '-0.04617', '0.4434', '0.602', '-0.03143', '-0.1512', '-0.2048', '0.4863', '0.7188', '0.133', '0.1952', '0.699', '0.37', '0.772', '0.3008', '-0.1725', '-0.1292', '0.5493', '1.14', '0.596', '-0.2947', '-0.2103', '0.251']",,,,,,,
mondo:0019268,epidermal disease,"['epidermal disease', 'rare epidermal disease']",,,79353,CN205920,,,,,,,,
mondo:0019269,ichthyosis,"['ichthyoses', 'non-syndromic ichthyosis', 'DOC', 'fish skin disease', 'disorder of cornification', 'ichthyosis (disease)', 'ichthyosis', 'fish scale disease']",1697,,79354,C0020757,,C84776,,D007057,,,10021198,0008064
mondo:0019270,erythrokeratoderma,,,,79355,,,,,,757.39,,10015280,
mondo:0019271,acrokeratoderma,,,,79356,,,,,,,,,
mondo:0019272,hereditary palmoplantar keratoderma,"['hereditary palmoplantar hyperkeratosis', 'hereditary PPK', 'hereditary palmoplantar keratosis', 'hereditary keratosis palmoplantaris']",,,79357,,,,,,757.39,,,
mondo:0019276,inherited epidermolysis bullosa,"['epidermolysis bullosa hereditaria', 'hereditary epidermolysis bullosa']",,,79361,,,,,,757.39,,,
mondo:0019277,epidermal appendage anomaly,,,,79362,,,,,,,,,
mondo:0019278,hair anomaly,,,,79363,,,,,,,,,
mondo:0019280,hypertrichosis,"['hypertrichosis (disease)', 'hypertrichosis']",420,,79365,C0020555,,,,D006983,,,10020864,0000998
mondo:0019281,isolated genetic hair shaft abnormality,['isolated hair shaft abnormality'],,,79366,,,,,,,,,
mondo:0019283,nail anomaly,"['epidermal appendage anomaly of nail', 'nail epidermal appendage anomaly']",,,79368,,,,,,,,10028684,
mondo:0019284,inherited isolated nail anomaly,"['nonsyndromic nail anomaly', 'nail disorder, nonsyndromic congenital', 'isolated nail anomaly']",0080683,,79369,,"['-0.10645', '0.05023', '-0.01293', '-0.02406', '0.1846', '-0.1061', '-0.004494', '0.0988', '-0.1376', '-0.146', '0.01744', '-0.01683', '-0.011795', '0.06174', '-0.0698', '-0.04037', '-0.0747', '-0.156', '-0.04572', '-0.4014', '-0.1066', '0.0683', '0.0806', '0.0422', '0.1626', '0.12317', '-0.09595', '-0.01706', '0.05484', '0.0013685', '0.1415', '-0.0754', '0.164', '0.1433', '0.09076', '-0.002882', '0.00784', '-0.03918', '-0.005093', '-0.27', '0.10846', '-0.12366', '0.02466', '-0.1456', '0.02492', '-0.12305', '-0.03796', '0.1335', '0.01537', '-0.1312', '0.02235', '-0.17', '0.0839', '-0.00787', '-0.243', '-0.04553', '0.1296', '-0.03232', '-0.2676', '-0.01971', '0.05283', '0.00457', '0.01132', '-0.0944', '0.039', '0.1108', '0.206', '0.1526', '-0.1254', '0.1917', '-0.1964', '0.04028', '0.0376', '-0.09534', '0.132', '0.05197', '-0.01483', '0.01833', '-0.0638', '-0.1725', '-0.1239', '0.0566', '-0.0727', '0.1617', '-0.013306', '-0.1396', '0.006077', '0.1109', '0.1741', '0.11475', '0.1118', '0.2108', '0.09174', '0.143', '0.3677', '0.03906', '0.1182', '-0.2996', '-0.012634', '0.2021']",,,,,,,
mondo:0019286,sebaceous gland anomaly,"['epidermal appendage anomaly of sebaceous gland', 'sebaceous gland epidermal appendage anomaly']",,,79372,,,,,,,,,
mondo:0019287,ectodermal dysplasia syndrome,"['ectodermal dysplasia', 'ectodermal dysplasia (select examples)', 'congenital ectodermal defect']",2121,,79373,C0013575,"['0.1142', '0.1279', '0.3953', '-0.1155', '0.727', '-0.2299', '0.3', '0.1212', '0.258', '-0.4624', '0.01035', '-0.881', '-0.8726', '-0.03204', '-0.1255', '0.5586', '0.561', '-0.16', '-0.1284', '-1.04', '-0.4082', '0.2634', '1.089', '-0.292', '0.1917', '0.1328', '-0.4639', '0.0798', '0.379', '-0.946', '0.3816', '0.06635', '-0.081', '0.6587', '0.5137', '-0.358', '-0.565', '0.2318', '-0.562', '-0.3618', '0.3167', '0.03128', '-0.2673', '-0.5405', '0.6504', '-0.6797', '0.2227', '0.004078', '0.688', '-0.0894', '0.364', '0.3267', '0.1387', '0.4128', '-0.4578', '-0.1725', '0.255', '-0.545', '-0.3997', '-0.02385', '0.1699', '0.405', '-0.1881', '0.12384', '-0.03867', '0.03354', '0.2827', '0.5996', '0.127', '0.9673', '-0.5635', '-0.29', '0.593', '0.001608', '0.1384', '0.389', '0.01193', '0.05798', '-0.2328', '-0.697', '0.236', '-0.0773', '0.3323', '-0.4263', '-0.3064', '-0.1472', '-0.123', '0.11884', '-0.1339', '-0.08215', '0.3206', '0.05157', '-0.08655', '0.3696', '0.3892', '-0.1307', '0.1976', '0.1186', '0.1285', '0.5684']",C84683,,D004476,757.31,,10010452,
mondo:0019288,skin pigmentation disorder,"['pigmentation disease of zone of skin', 'pigmentation disease', 'zone of skin pigmentation disease']",10123,,79374,,,C34557,1000755,D010859,709.09,,,
mondo:0019289,hyperpigmentation of the skin,,,,79375,,,,0009047,,709.09,,,0000953
mondo:0019290,hypopigmentation of the skin,"['hypomelanoses', 'hypopigmentation of the skin (disease)', 'hypomelanosis', 'hypopigmentation of the skin']",,,79376,,,,,D017496,,,10040868,0001010
mondo:0019292,dermis elastic tissue disorder,,,,79378,CN227616,,,,,,,,
mondo:0019293,skin vascular disease,"['superficial vasculature disease', 'vasculature skin disease', 'skin vascular disorder', 'vascular skin disease']",9540,,79379,C0162819,,C35254,,D017445,709.1,,10062171,
mondo:0019294,mixed dermis disorder,,,,79380,CN227617,,,,,,,,
mondo:0019296,subcutaneous tissue disorder,"['superficial fascia disease', 'disease of superficial fascia', 'superficial fascia disease or disorder', 'disorder of superficial fascia']",,,79382,C1290008,,,,,,,,
mondo:0019297,lymphedema,"['lymphatic oedema', 'lymphoedema', 'lymphatic oedema (morphologic abnormality)', 'lymphatic edema', 'lymphatic edema (morphologic abnormality)']",4977,,79383,C0024236,,C3207,,D008209,457.1,,10025282,
mondo:0019303,premature aging syndrome,"['premature ageing', 'premature aging']",,,79389,,,,,D019588,,,10063493,
mondo:0019306,congenital non-bullous ichthyosiform erythroderma,"['CIE', 'lamellar ichthyosis', 'nonbullous congenital ichthyosiform erythroderma', 'erythrodermic ichthyosis', 'congenital ichthyosiform erythroderma (disease)', 'alligator skin', 'non-bullous congenital ichthyosiform erythroderma', 'lamellar desquamation of the newborn', 'congenital ichthyosiform erythroderma', 'ichthyosiform erythroderma', 'congenital non bullous ichthyosiform erythroderma']",1699,,79394,,"['-0.3118', '0.0974', '-0.2048', '-0.313', '0.8315', '-0.732', '-0.568', '0.06305', '-0.029', '-0.2866', '0.4963', '-0.10364', '0.0322', '0.369', '-0.3335', '0.0625', '0.2854', '-0.225', '-0.1527', '-1.331', '-0.5366', '0.0877', '0.4863', '0.184', '0.05295', '0.328', '-1.158', '0.1409', '-0.3445', '-0.07117', '0.969', '-0.4736', '-0.1608', '0.5107', '-0.236', '0.0554', '-0.3374', '-0.3237', '-0.3884', '0.02966', '0.28', '-0.004795', '-0.274', '0.4807', '0.3591', '-0.6577', '-0.3132', '-0.547', '0.3884', '0.1394', '-0.2205', '-0.337', '0.4648', '-0.387', '-0.5483', '-0.10187', '0.4192', '-0.397', '-0.1857', '-0.324', '-0.2544', '0.06125', '-0.662', '-0.331', '0.6475', '0.02385', '0.654', '0.07574', '0.0832', '0.4438', '-0.08246', '-0.4866', '0.336', '0.09607', '0.3052', '-0.1016', '0.349', '-0.851', '0.381', '-0.06033', '0.0287', '-0.005577', '-0.2106', '0.3633', '-0.03183', '-0.01936', '0.0241', '0.4944', '-0.03026', '0.8584', '0.2018', '0.4465', '0.0694', '0.7227', '0.4797', '0.12177', '-0.2803', '-0.2815', '-0.1287', '-0.1552']",C84805,,D017490,,,,0007431
mondo:0019307,generalized junctional epidermolysis bullosa non-Herlitz type,"['junctional epidermolysis bullosa, generalized intermediate', 'GABEB', 'junctional epidermolysis bullosa, generalised intermediate', 'generalized junctional epidermolysis bullosa, non-Herlitz type', 'junctional epidermolysis bullosa generalisata mitis', 'JEB, generalized intermediate', 'JEB-nH gen', 'generalised junctional epidermolysis bullosa, non-Herlitz type', 'junctional epidermolysis bullosa non-Herlitz type', 'generalised atrophic benign epidermolysis bullosa', 'JEB, generalised intermediate', 'junctional epidermolysis bullosa, Disentis type', 'generalized atrophic benign epidermolysis bullosa']",0060738,,79402,,"['0.7505', '0.0718', '-0.3572', '-0.2404', '0.436', '-0.4155', '-0.3887', '0.3862', '-0.06915', '-0.742', '0.1875', '-0.715', '-0.812', '0.116', '-0.4866', '0.1638', '0.2174', '-1.093', '-0.3696', '-0.8984', '-0.2433', '-0.06525', '0.763', '0.3547', '0.4778', '0.471', '-0.912', '0.5034', '-0.3208', '-0.3606', '0.4639', '-0.3887', '-0.427', '0.1176', '0.0848', '0.2173', '-1.124', '0.0959', '0.8984', '-0.548', '0.5166', '-0.4958', '-0.03555', '-0.2197', '-0.05197', '-0.08105', '-0.2815', '-0.10913', '0.3242', '-0.1792', '-0.506', '-0.707', '0.843', '-0.08307', '0.214', '-0.5425', '-0.3936', '0.847', '-0.555', '-0.1499', '-0.2153', '0.4275', '0.05542', '0.013504', '0.8784', '0.689', '0.007996', '0.491', '-0.4868', '0.4836', '-0.2023', '-0.05573', '-0.375', '0.04614', '0.1808', '-0.1882', '0.1674', '0.0357', '-0.03186', '-0.3743', '-0.544', '-0.01186', '-0.1963', '-0.4666', '0.519', '0.369', '-0.9355', '0.6074', '0.657', '0.3765', '-0.3772', '0.4177', '0.05075', '0.736', '0.292', '0.446', '0.1421', '-0.3816', '0.95', '0.05322']",,,,,,,
mondo:0019308,junctional epidermolysis bullosa inversa,"['JEB-I', 'inverse JEB', 'EBJ-I']",,,79405,C2673610,,,,,,,,
mondo:0019309,late-onset junctional epidermolysis bullosa,"['JEB-lo', 'EB progressive']",,,79406,CN205949,,,,,,,,
mondo:0019310,recessive dystrophic epidermolysis bullosa inversa,"['RDEB-I', 'inverse recessive dystrophic epidermolysis bullosa', 'dystrophic epidermolysis bullosa inversa', 'inverse RDEB']",,,79409,CN205951,"['0.74', '0.0709', '-0.384', '-0.1698', '0.2705', '-0.2167', '-0.378', '0.6475', '-0.221', '-0.593', '0.1735', '-0.4321', '-0.9453', '0.2522', '-0.58', '-0.168', '0.1649', '-0.8696', '-0.1865', '-0.6206', '-0.3296', '-0.01309', '0.4119', '0.4697', '0.0865', '0.4207', '-0.86', '0.586', '-0.501', '-0.524', '0.3035', '-0.2427', '-0.3704', '0.01248', '-0.1193', '-0.2344', '-1.067', '0.1511', '0.7817', '-0.2834', '0.463', '-0.4648', '-0.01482', '0.0293', '0.09875', '-0.2625', '-0.2446', '0.2252', '0.1603', '-0.1881', '-0.4114', '-0.8013', '0.4106', '-0.2786', '-0.2249', '-0.3625', '-0.153', '0.8945', '-0.4106', '-0.0812', '0.1716', '0.5835', '-0.3425', '0.2384', '0.712', '0.5356', '0.6294', '0.2411', '-0.548', '0.2708', '-0.02931', '0.1499', '-0.3896', '-0.04767', '0.1965', '-0.0917', '-0.007294', '0.1962', '-0.3206', '-0.187', '-0.642', '-0.00815', '0.0719', '-0.273', '0.214', '0.2935', '-0.7188', '0.5044', '0.4363', '0.05573', '-0.5205', '0.373', '0.1761', '0.4844', '0.08997', '0.309', '0.3762', '-0.4111', '0.564', '-0.125']",,,,,,,
mondo:0019311,wooly hair nevus,['wooly hair nevus'],,,79414,C0343114,,,,,,,,
mondo:0019312,Hermansky-Pudlak syndrome,"['HPS (Hermansky Pudlak syndrome)', 'Hermansky Pudlak syndrome', 'HPS']",3753,,79430,,"['0.3757', '-0.1951', '-0.6343', '-0.2233', '0.4187', '0.0391', '0.1082', '0.3428', '0.1713', '0.1469', '0.12177', '-0.1372', '-0.1183', '0.2932', '-0.3418', '-0.461', '0.3306', '0.169', '0.2979', '-0.973', '-0.6797', '-0.756', '0.5947', '-0.5615', '-0.1233', '-0.2238', '-0.353', '0.9424', '0.5444', '0.2454', '0.277', '-0.01582', '0.06366', '0.3872', '0.009384', '-0.32', '0.0628', '-0.573', '0.0766', '0.3328', '0.725', '-0.4675', '0.2043', '0.1892', '0.3413', '0.01196', '0.0053', '-0.1069', '0.543', '-0.1732', '0.1835', '-0.3994', '0.241', '0.3657', '0.3562', '0.635', '0.1458', '-0.1495', '-0.663', '-0.4128', '-0.4988', '-0.1957', '0.03735', '-0.2825', '0.2168', '0.392', '0.6157', '-0.03683', '-0.7803', '0.1368', '-0.1514', '-0.7075', '-0.05267', '-0.4385', '1.02', '-0.0897', '0.627', '-0.5483', '0.5483', '0.1895', '-0.251', '-0.542', '-0.2441', '0.579', '-0.534', '-0.1804', '0.1152', '0.2573', '0.4653', '-0.506', '0.4285', '0.947', '-0.02357', '0.00917', '0.7773', '0.3394', '-0.0755', '-0.3503', '-0.1621', '-0.00011873']",C37261,,D022861,270.2,E70.331,10071775,
mondo:0019313,lymphatic malformation,"['lymphedema, hereditary', 'hereditary lymphedema']",0050580,,,,,,,,757.0,Q82.0,,
mondo:0019314,cutaneous mastocytoma,"['multiple mastocytoma', 'cutaneous local mastocytoma', 'solitary mastocytoma']",,,79455,,,,,D054705,,,,
mondo:0019315,diffuse cutaneous mastocytosis,"['diffuse cutaneous mastocytosis', 'diffuse cutaneous maculopapulous mastocytosis', 'DCM']",3665,,79456,C0024901,,C3218,,,,,10012812,
mondo:0019316,maculopapular cutaneous mastocytosis,"['urticaria pigmentosa', 'Paucicellular mastocytosis', 'telangiectasia macularis eruptive perstans', 'telangiectatic cutaneous mastocytosis', 'UP/MPCM', 'urticaria pigmentosa/maculopapular cutaneous mastocytosis']",12309,,79457,C0042111,,C3433,,,708.8,,10046752,
mondo:0019317,follicular atrophoderma-basal cell carcinoma,,,,79459,CN205972,,,,,,,,
mondo:0019318,inflammatory linear verrucous epidermal nevus,"['ILVEN', 'linear verrucose epidermal nevus', 'inflammatory linear verrucous epidermal naevus']",,,79466,C0473574,,,,,,,,
mondo:0019319,verrucous nevus,['verrucous Epidermal Nevus'],,,79467,C0362030,,C4674,,,,,,
mondo:0019320,acanthokeratolytic verrucous nevus,['verrucous nevus acanthokeratolytic'],,,79468,CN205975,,,,,,,,
mondo:0019321,atypical Werner syndrome,['atypical progeroid syndrome'],,,79474,CN205977,,,,,,,,
mondo:0019322,pemphigus vegetans,,,,79479,CN205981,,,0008613,,,L10.1,10057053,
mondo:0019323,pemphigus erythematosus,"['seborrheic pemphigus', 'Senear-Usher syndrome']",,,79480,C0263312,,,0008603,,,L10.4,10058917,
mondo:0019324,pemphigus foliaceus,['PF'],0080850,,79481,C0263313,,,0008601,,,,10057069,
mondo:0019325,phakomatosis cesioflammea,['phakomatosis pigmentovascularis type 2'],,,79483,CN205984,,,,,759.6,,,
mondo:0019326,phakomatosis cesiomarmorata,['phakomatosis pigmentovascularis type 5'],,,79484,CN205985,,,,,759.6,,,
mondo:0019327,phakomatosis spilorosea,['phakomatosis pigmentovascularis type 3'],,,79485,CN205986,,,,,759.6,,,
mondo:0019328,macrocystic lymphatic malformation,"['cavernous lymphatic malformation', 'cavernous lymphangioma', 'macrocystic lymphangioma']",,,79489,,,C53316,,,,,,
mondo:0019329,microcystic lymphatic malformation,"['microcystic infiltrating lymphatic malformation', 'superficial lymphangioma', 'capillary lymphangioma', 'microcystic lymphangioma', 'cutaneous lymphangioma circumscriptum', 'capillary lymphatic malformation', 'superficial lymphatic malformation']",,,79490,,,,,,,,,
mondo:0019330,pili gemini,['pili multigemini'],,,79492,,,,,C537188,704.8,,,
mondo:0019332,punctate palmoplantar keratoderma type 1,"['keratodermia palmoplantaris papulosa, Buschke-Fischer-Brauer type', 'keratoderma, palmoplantar punctate type 1', 'punctate palmoplantar keratoderma type I', 'Brauer-Buschke-Fischer syndrome', 'type I punctate palmoplantar keratoderma', 'PPKP1', 'Buschke-Fischer-Brauer syndrome']",,,79501,CN205995,"['-0.05692', '-0.0944', '-0.946', '0.3318', '-0.161', '-0.4421', '-0.4868', '0.5044', '0.0931', '-0.257', '-0.1335', '-0.2152', '-0.08124', '0.075', '0.161', '0.2494', '0.11816', '-0.5615', '0.0917', '-0.8076', '-0.05396', '-0.2378', '0.4456', '0.1415', '0.0823', '0.6094', '-0.4553', '0.3174', '0.01697', '-0.6035', '0.856', '-0.4824', '-0.5117', '0.5215', '0.3025', '-0.8267', '-0.03494', '-0.1064', '0.642', '0.3943', '0.3643', '-0.5312', '0.4673', '0.1459', '0.2303', '-0.1211', '-0.0555', '-0.1516', '0.3972', '-0.5337', '-0.3062', '0.1575', '0.07513', '0.3682', '-0.5303', '0.2695', '0.8325', '0.3152', '-0.2136', '-0.4128', '-0.04196', '0.1895', '-0.1962', '-0.199', '-0.252', '0.463', '0.314', '0.9307', '0.1938', '0.949', '-0.401', '-0.3625', '0.4585', '0.343', '0.7173', '0.32', '-0.499', '-0.0833', '0.2559', '-0.4397', '-0.2302', '0.1008', '-0.2053', '0.3445', '0.01851', '-0.08655', '-0.1516', '0.8174', '0.2852', '0.5293', '0.2732', '0.0656', '0.3123', '0.1635', '0.589', '-0.1792', '0.669', '-0.2029', '0.0977', '-0.501']",,,,,,,
mondo:0019333,autosomal recessive hyperinsulinism due to SUR1 deficiency,['autosomal recessive hyperinsulinemic hypoglycemia due to SUR1 deficiency'],,,79643,CN206002,"['-0.04727', '0.3604', '-0.322', '0.07623', '-0.2708', '-0.4155', '-0.0645', '0.3608', '0.2095', '-0.2021', '-0.1896', '-0.09503', '0.2267', '0.003304', '-0.2913', '-0.1564', '0.02081', '-0.02701', '-0.1714', '-0.6084', '-0.04987', '-0.1553', '0.2532', '-0.0396', '-0.1339', '0.1482', '0.1495', '-0.1545', '0.0647', '-0.304', '0.2761', '0.1348', '0.2158', '0.213', '-0.364', '0.2135', '0.0451', '-0.3716', '-0.397', '0.1841', '-0.1525', '-0.2703', '0.2834', '0.1054', '-0.2922', '0.0893', '-0.3362', '-0.1051', '-0.1626', '0.362', '0.01654', '0.04645', '0.10034', '-0.0339', '-0.1729', '0.12286', '0.156', '-0.1783', '-0.1763', '0.3933', '0.1766', '0.1015', '-0.07697', '-0.3113', '-0.1059', '0.07886', '0.3428', '0.385', '-0.3105', '0.4246', '0.09314', '0.1616', '0.02747', '-0.335', '0.3086', '0.01502', '0.09155', '-0.1404', '-0.2998', '0.2654', '-0.1827', '0.1635', '-0.1877', '-0.1719', '0.1654', '0.3586', '0.0705', '0.1046', '0.5264', '0.08167', '0.4253', '0.1931', '0.0582', '-0.1908', '0.3442', '0.0794', '0.1772', '-0.561', '0.04156', '0.1901']",,,,,,,
mondo:0019334,autosomal recessive hyperinsulinism due to Kir6.2 deficiency,['autosomal recessive hyperinsulinemic hypoglycemia due to Kir6.2 deficiency'],,,79644,CN206003,"['-0.05563', '0.3398', '-0.3076', '0.0826', '-0.2435', '-0.449', '-0.03078', '0.3577', '0.2058', '-0.192', '-0.2274', '-0.11414', '0.2394', '-0.0004377', '-0.3079', '-0.2162', '0.0445', '-0.02286', '-0.1387', '-0.6963', '-0.05298', '-0.1114', '0.269', '-0.05377', '-0.145', '0.1935', '0.1646', '-0.1075', '0.0784', '-0.2659', '0.2688', '0.1774', '0.2255', '0.2434', '-0.3835', '0.1909', '0.04987', '-0.3464', '-0.427', '0.2094', '-0.1525', '-0.2249', '0.3135', '0.099', '-0.2913', '0.0933', '-0.3408', '-0.1265', '-0.1456', '0.3452', '0.03983', '0.0463', '0.10004', '-0.0359', '-0.2036', '0.11743', '0.12476', '-0.175', '-0.1862', '0.406', '0.1721', '0.1085', '-0.03467', '-0.3184', '-0.06415', '0.0684', '0.3843', '0.3945', '-0.3232', '0.4128', '0.1359', '0.0994', '0.0776', '-0.366', '0.3108', '0.007233', '0.1321', '-0.1464', '-0.3018', '0.2319', '-0.2069', '0.167', '-0.1886', '-0.1709', '0.1747', '0.3542', '0.09094', '0.09296', '0.5493', '0.0746', '0.4448', '0.2085', '0.03162', '-0.1821', '0.34', '0.1139', '0.1914', '-0.5425', '0.05072', '0.2008']",,,,,,,
mondo:0019335,mild hyperphenylalaninemia,"['mHPA', 'non-PKU HPA', 'mild HPA']",,,79651,,"['-0.3748', '0.2927', '0.3154', '-0.3164', '0.1737', '-0.119', '-0.2954', '0.3271', '-0.2322', '0.1711', '-0.2014', '-0.1656', '0.2192', '-0.1349', '-0.04807', '-0.403', '-0.02962', '0.02028', '-0.2169', '-0.5527', '0.03098', '-0.1898', '0.409', '-0.01163', '-0.02634', '-0.07043', '-0.01648', '-0.11993', '-0.01494', '-0.1329', '-0.05115', '0.0946', '0.3337', '0.2382', '-0.2825', '-0.0934', '-0.2467', '-0.1013', '-0.0489', '-0.2832', '0.2039', '-0.5054', '0.123', '-0.2993', '-0.2742', '-0.359', '0.2256', '-0.0586', '0.09686', '0.3801', '-0.02905', '-0.02733', '-0.0714', '-0.1986', '-0.08765', '-0.10474', '0.03775', '-0.1543', '-0.421', '0.1231', '0.1298', '0.0795', '0.587', '-0.1555', '0.2018', '0.1688', '0.196', '0.04233', '-0.3716', '0.1588', '-0.05743', '0.1766', '-0.07025', '-0.05365', '0.135', '0.4102', '0.176', '-0.285', '-0.3284', '-0.227', '0.04727', '0.10156', '-0.0926', '0.1918', '0.3206', '0.2456', '-0.1886', '0.07715', '0.517', '0.2942', '0.464', '0.4585', '-0.02876', '-0.1777', '0.1897', '0.4739', '0.1868', '-0.403', '0.1075', '0.2013']",,,,,,,
mondo:0019336,Gardner syndrome,"['polyposis coli and multiple hard and soft tissue tumours', 'polyposis coli and multiple hard and soft tissue tumors', 'intestinal polyposis, osteomas, sebaceous cysts', 'Gardner^s syndrome', 'Gardner syndrome']",,,79665,C0017097,,C6728,,D005736,759.89,,10017727,
mondo:0019337,autoimmune bullous skin disease,['bullous skin disease'],8502,,79669,CN206006,,,1000673,,694.9,,,
mondo:0019338,sarcoidosis,"['Besnier-Boeck-Schaumann disease', 'lymphogranulomatosis', 'sarcoid', 'Boeck^s sarcoid', 'Boeck sarcoid']",11335,,797,C0036202,"['0.0525', '0.3508', '-0.8584', '0.186', '0.03278', '-0.3682', '0.5283', '0.258', '-0.6655', '0.04422', '-0.0941', '0.1293', '-0.76', '0.4578', '0.02736', '-0.0423', '-0.251', '0.06055', '0.01706', '-0.2283', '-0.1733', '-0.4329', '0.62', '-0.8794', '-0.4482', '0.0167', '0.001593', '0.4307', '-0.001072', '0.3867', '0.4417', '-0.198', '0.4568', '0.1261', '-0.1288', '-0.4407', '-0.477', '0.1895', '0.307', '-0.0368', '0.3203', '0.1823', '0.4482', '-0.3386', '-0.1313', '-0.01828', '-0.2922', '-0.198', '-0.68', '0.373', '-0.143', '0.387', '0.7866', '-0.07623', '-0.212', '0.3542', '0.01797', '0.3965', '-0.2153', '-0.7007', '-0.005753', '0.3767', '-0.545', '-0.1963', '0.01752', '0.001957', '0.1677', '0.681', '-0.2144', '0.5415', '0.1754', '0.1458', '0.01715', '-0.0792', '0.2737', '0.3257', '-0.0766', '0.1261', '-0.2091', '-0.2103', '0.119', '-0.7476', '-0.0988', '0.2328', '0.0156', '-0.56', '0.1987', '0.3152', '0.0749', '0.4275', '0.27', '-0.3772', '-0.3872', '-0.1501', '0.952', '0.11163', '0.02913', '0.0995', '-0.163', '0.2471']",C34995,,D012507,135,,10039486,
mondo:0019339,"47,XYY syndrome","['XYY karyotype', '47,XYY syndrome', 'XYY syndrome', '47,XYY', '47, XYY syndrome', 'Double Y syndrome', 'YY syndrome', 'disomy Y', 'Y disomy', 'Double Y']",,,8,,,C85237,,C535317,,,10056894,
mondo:0019340,scleroderma,"['dermatosclerosis', 'scleroderma', 'scleroderma (disease)']",419,,801,,,C26746,,,,,10039710,0100324
mondo:0019342,Seckel syndrome,"['Seckel-type Dwarfism', 'bird-headed dwarfism', 'Virchow-Seckel dwarfism', 'Harper^s syndrome', 'SCKL', 'nanocephalic Dwarfism']",0050569,,808,C0265202,"['-0.3918', '0.475', '0.2172', '-0.4626', '0.4504', '0.001396', '-0.1947', '0.676', '-0.7476', '-0.6074', '-0.05902', '0.4565', '0.3513', '0.007397', '0.0833', '-0.07996', '0.499', '-0.2332', '-0.4526', '-0.5264', '0.01688', '0.00946', '0.2803', '-0.4067', '-0.05438', '-0.1936', '-0.3477', '0.1938', '0.447', '-0.4934', '-0.11505', '-0.004734', '0.937', '0.0707', '-0.05106', '0.0001855', '-0.3757', '-0.728', '-0.4028', '0.04355', '-0.0783', '-0.07336', '-0.0439', '-0.4976', '-0.03503', '-0.607', '-0.4385', '0.010704', '0.3914', '-0.1531', '0.2028', '0.0953', '-0.3884', '0.2401', '0.1621', '-0.2937', '0.1638', '-0.1214', '-0.0852', '0.591', '0.2212', '-0.0916', '-0.0464', '0.2512', '-0.1345', '0.03714', '-0.1364', '0.2202', '0.05237', '0.1509', '-0.3232', '-0.1098', '-0.11884', '-0.1045', '-0.05304', '-0.3567', '0.2617', '0.02158', '-0.3774', '-0.10364', '0.2366', '0.17', '-0.5713', '0.2969', '-0.04095', '0.076', '0.2783', '0.639', '0.4302', '0.8477', '0.029', '0.4172', '-0.249', '-0.4468', '0.573', '0.3577', '0.3657', '-0.4468', '0.7217', '0.04605']",C125488,,,759.89,,,
mondo:0019344,antisynthetase syndrome,"['AS syndrome', 'anti-Jo1 syndrome']",0080744,,81,C2609059,,,1001982,C537778,279.49,,10068801,
mondo:0019345,shigellosis,"['Shigella flexneri infectious disease', 'Shigella boydii infectious disease', 'Shigella gastroenteritis', 'Shigella sonnei infectious disease', 'bacillary dysentery']",12385,,810,,,C157978,0005585,D004405,004.9,A03,10054178,
mondo:0019346,sialidosis type 1,"['lipomucopolysaccharidosis', 'cherry red spot myoclonus syndrome', 'myoclonus cherry red spot syndrome', 'Normomorphic sialidosis', 'cherry-red spot-myoclonus syndrome', 'sialidosis type I']",,,812,CN206021,,,,,,,,
mondo:0019347,peeling skin syndrome,"['idiopathic deciduous skin', 'peeling skin disease', 'PSS', 'deciduous skin', 'familial continuous skin peeling syndrome', 'familial continuous skin peeling', 'keratosis exfoliativa congenita', 'skin peeling syndrome']",0060283,,817,,,,,,757.39,,,
mondo:0019349,Sotos syndrome,"['distinctive facial appearance, overgrowth in childhood, and learning disabilities or delayed development', 'cerebral gigantism syndrome', 'cerebral gigantism', 'Sotos^ syndrome']",14748,,821,CN239475,"['0.2659', '-0.1967', '0.1477', '-0.2773', '0.448', '-0.561', '0.3428', '1.357', '-0.923', '-0.3584', '-0.1549', '-0.1495', '0.2986', '0.03004', '-0.2744', '0.2369', '0.4402', '-0.2732', '-0.2452', '-0.02422', '0.01271', '-0.482', '0.3352', '-0.1082', '0.7812', '0.0879', '-0.1458', '-0.0568', '0.3416', '-0.1909', '0.6694', '0.0837', '0.2214', '0.4153', '0.2659', '0.3079', '-0.2036', '0.07153', '-0.264', '-0.3882', '-0.2043', '0.0942', '0.09595', '-0.2328', '0.399', '-0.582', '0.0846', '0.2087', '0.4504', '0.00146', '-0.5522', '0.548', '-0.4185', '0.1322', '-0.4077', '-0.3423', '-0.3943', '-0.1781', '0.37', '-0.1719', '0.2462', '0.01659', '-0.1023', '-0.2388', '0.01149', '0.1829', '0.1012', '0.2467', '-0.1001', '0.719', '-0.3232', '0.3223', '-0.1682', '0.0832', '-0.1796', '-0.502', '0.2778', '0.142', '-0.01813', '-0.4797', '0.1921', '-0.489', '-0.822', '0.4023', '-0.07117', '-0.0523', '0.0521', '-0.3857', '0.5586', '0.564', '0.0546', '0.5073', '-0.02838', '0.1904', '0.2495', '-0.0524', '0.572', '-0.6035', '0.6353', '-0.3022']",C75019,,D058495,,,10064387,
mondo:0019350,hereditary spherocytosis,"['Minkowski-Chauffard disease', 'congenital spherocytosis', 'congenital spherocytic hemolytic anemia', 'congenital spherocytic hemolytic anaemia', 'spherocytic anemia', 'spherocytic anaemia', 'Minkowski Chauffard syndrome']",12971,,822,CN206031,"['0.2411', '-0.1743', '-0.11993', '0.007793', '0.3918', '-0.04996', '-0.09753', '0.7915', '0.2325', '0.10376', '-0.1609', '0.718', '-0.05267', '0.2676', '0.1514', '-0.2502', '-0.2233', '-0.342', '0.3167', '-0.7983', '-0.3665', '0.2368', '0.6665', '0.219', '0.1361', '-0.3162', '-0.1329', '-0.07385', '-0.02583', '-0.7173', '0.1385', '-0.2034', '0.2229', '0.7305', '-0.538', '-0.3123', '-0.236', '-0.612', '0.07623', '-0.4219', '-0.202', '-0.1523', '1.226', '-0.4778', '-0.10425', '0.1702', '-0.487', '-0.1991', '-0.1542', '-0.08136', '0.05334', '-0.3096', '-0.02852', '0.03918', '-0.2064', '0.1044', '0.06174', '-0.1608', '-0.2345', '0.5874', '0.6304', '-0.1224', '0.3813', '0.0001594', '0.361', '-0.619', '0.3696', '0.7954', '-0.2842', '0.3616', '0.316', '0.527', '-0.2084', '-0.2225', '0.3245', '-0.2025', '0.3152', '-0.429', '0.4749', '-0.568', '0.06366', '-0.524', '-0.798', '-0.0647', '-0.2097', '0.6484', '-0.1328', '0.2378', '-0.10394', '-0.2295', '0.3682', '0.199', '-0.38', '-0.5337', '0.777', '0.844', '0.2211', '-0.5264', '-0.419', '-0.6567']",C97074,,D013103,282.0,D58.0,10019904,
mondo:0019351,isolated spina bifida,"['cleft spine', 'open spine', 'nonsyndromic spina bifida (disease)']",,,823,,"['0.0659', '0.09033', '-0.0852', '-0.1277', '0.62', '0.05707', '-0.3516', '0.3955', '-0.8706', '0.1788', '0.04544', '-0.189', '-0.2893', '0.5923', '-0.5645', '-0.1913', '-0.644', '-0.525', '-0.3142', '-0.8506', '-0.09766', '-0.4468', '0.2272', '0.1292', '-0.4924', '-0.477', '0.166', '-0.0767', '0.224', '0.2776', '0.207', '-0.674', '0.521', '-0.2693', '0.002583', '-0.0938', '0.0954', '0.2986', '0.538', '-0.2356', '0.2563', '-0.4019', '0.1876', '0.06866', '-0.6523', '-0.1632', '0.19', '-0.2369', '-0.3267', '0.1294', '-0.3499', '-0.3145', '0.0057', '-0.6826', '-0.8853', '0.3977', '-0.4106', '0.7007', '0.2854', '0.01205', '-0.334', '-0.1592', '-0.3555', '0.5234', '0.03928', '0.8325', '0.4329', '0.08154', '0.1367', '0.828', '0.0405', '0.4478', '-0.546', '-0.907', '-0.2307', '0.298', '0.2212', '0.0941', '0.3574', '-0.07007', '-0.8105', '-0.01859', '-0.0546', '0.4258', '0.2438', '0.4932', '-0.03117', '0.1329', '0.4094', '0.10126', '-0.38', '0.5513', '0.1808', '0.2925', '0.4993', '-0.2223', '0.448', '-0.2852', '-0.006355', '-0.01718']",,,,,,10041524,
mondo:0019353,Stargardt disease,"['Stargardt disease 1', 'Stargardt macular dystrophy', 'Stargardt 1', 'juvenile onset macular degeneration', 'fundus flavimaculatus']",0050817,,827,C1855465,"['-0.5034', '-0.441', '-0.2202', '0.427', '0.2188', '0.0729', '-0.548', '0.238', '-0.4607', '-0.06714', '-0.2766', '-0.0955', '-0.2166', '0.505', '-0.1934', '-0.001509', '0.2311', '0.3843', '-0.0847', '-0.4426', '-0.6196', '-0.1782', '-0.0919', '0.03317', '-0.1583', '-0.2852', '-0.468', '-0.1824', '-0.392', '0.01582', '0.8115', '-0.2455', '-0.0847', '0.3718', '0.2927', '0.2426', '0.4365', '-0.3215', '-0.2025', '-0.3792', '-0.12256', '-0.305', '0.423', '-0.2305', '-0.584', '-0.8784', '-0.0539', '-0.2322', '-0.3748', '0.4329', '0.423', '-0.07367', '0.452', '-0.706', '0.2542', '-0.131', '0.707', '-0.335', '-0.738', '-0.007607', '-0.1819', '-0.0774', '0.1401', '0.1973', '-0.3945', '0.04684', '1.009', '0.327', '0.4463', '0.2646', '-0.4004', '-0.397', '0.06415', '0.188', '0.893', '-0.0797', '-0.04858', '-0.0004065', '-0.0917', '-0.642', '0.751', '-0.9243', '0.10175', '0.804', '-0.5186', '-0.5693', '0.5596', '0.1317', '0.3364', '0.4421', '0.22', '0.141', '-0.06177', '0.175', '0.1625', '0.1884', '0.0673', '-0.3955', '-0.3142', '-0.1437']",C85078,,D000080362,,H35.5,10062766,
mondo:0019354,Stickler syndrome,['hereditary progressive arthroophthalmopathy'],0080046,,828,C0265253,"['0.906', '-0.04974', '-0.4019', '0.276', '0.3682', '-0.2708', '-0.1512', '1.013', '-0.965', '-0.7026', '0.2695', '-0.7124', '-0.1191', '0.573', '-0.0914', '-0.1364', '-0.4102', '0.006016', '-0.4265', '-0.03842', '-0.1459', '0.00872', '0.7188', '0.4143', '0.001149', '0.62', '-0.7026', '0.2201', '0.869', '0.572', '0.27', '0.05856', '-0.02298', '0.898', '-0.3267', '-0.02985', '-0.01814', '-0.109', '-0.1498', '-0.09937', '0.654', '0.3228', '-0.254', '-0.07465', '-0.2856', '-0.3843', '0.1526', '-0.2727', '0.1812', '-0.237', '-0.03403', '0.0885', '0.448', '-0.2795', '0.08093', '-0.709', '-0.4375', '0.2478', '-0.288', '-0.3765', '0.8667', '0.3198', '-0.4238', '0.238', '-0.1251', '-0.05707', '0.2036', '0.4163', '-0.1924', '0.569', '0.012375', '0.1835', '-0.4846', '-0.815', '0.4746', '0.05984', '0.1313', '0.2947', '0.3047', '0.66', '0.02568', '-0.438', '-0.1923', '1.437', '-0.4941', '0.3093', '0.3125', '0.844', '0.057', '0.3022', '-0.4106', '0.5986', '-0.2043', '0.09955', '0.59', '-0.3762', '0.884', '-0.1624', '-0.1183', '0.524']",C74984,,,759.89,,10063402,
mondo:0019355,adult-onset Still disease,"['AOSD', 'Wissler-Fanconi syndrome', 'adult Still^s disease', 'adult-onset Still^s disease', 'adult-onset Still disease', 'Still^s disease adult onset', 'adult onset Still^s disease']",14256,,829,CN206037,,,0007135,D016706,759.89,,10064056,
mondo:0019356,urogenital tract malformation,,,,83001,,,,,,,Q60-Q64,,
mondo:0019357,congenital narrowing of cervical spinal canal,"['congenital cervical spinal stenosis', 'congenital stenosis of the cervical spine']",,,831,,,,,,,,,
mondo:0019358,encephalopathy due to sulfite oxidase deficiency,,,,833,C4275019,"['-0.3562', '0.06836', '-0.194', '0.6587', '0.10516', '-0.44', '0.1471', '0.2527', '-0.8555', '-0.2445', '-0.3442', '-0.08154', '0.3635', '-0.42', '0.1218', '-0.1432', '0.5034', '-0.3635', '-0.2463', '-0.653', '0.2817', '-0.355', '-0.02464', '0.006252', '-0.08936', '-0.6006', '-0.2998', '0.1422', '-0.2372', '-0.005604', '0.6387', '-0.02739', '-0.1863', '0.5513', '-0.1846', '0.3118', '0.012695', '-0.251', '-0.3203', '0.1164', '0.3774', '-0.9937', '0.2756', '-0.11475', '-0.09326', '0.1178', '0.247', '-0.01369', '-0.2915', '0.3962', '0.0504', '-0.2365', '-0.11584', '-0.2039', '0.4639', '-0.491', '0.3374', '0.1569', '0.4243', '0.598', '-0.263', '-0.000554', '0.08856', '-0.3994', '0.10004', '-0.02684', '0.1481', '0.00861', '-0.278', '0.895', '-0.1716', '0.1081', '0.3853', '-0.0213', '0.06726', '0.665', '0.1515', '-0.4856', '-0.1796', '0.3286', '0.0849', '0.416', '-0.05283', '0.3071', '-0.1372', '0.845', '-0.163', '0.5186', '0.4744', '0.196', '-0.2418', '0.652', '0.06537', '0.1643', '0.3176', '0.325', '-0.1986', '-0.705', '0.6084', '-0.1754']",,,,,,,
mondo:0019359,Rocky mountain spotted fever,"['Fiebre manchada', 'Tick typhus', 'sao Paulo typhus', 'Brazillian spotted', 'RMSF', 'Fiebre maculosa', 'Choix', 'exanthematic typhus of sao Paulo', 'Tobia fever', 'So Paulo fever']",0050052,,83311,C0035793,,C128410,,D012373,,,10039207,
mondo:0019360,rickettsialpox,"['vesicular rickettsiosis', 'Rickettsia akari spotted fever']",11103,,83312,C0035597,,,,D012288,083.2,,10039137,
mondo:0019362,epidemic louse-borne typhus,"['sylvatic typhus', 'epidemic typhus', 'epidemic louse-borne typhus', 'epidemic typhus fever', 'typhus']",0050480,,83314,,,C84689,,,,,10014979,
mondo:0019364,pseudotyphus of California,,,,83316,,,,,,,,,
mondo:0019365,scrub typhus,"['Japanese river fever', 'Mite-borne typhus', 'chigger-borne typhus', 'scrub mite-borne typhus', 'scrub (mite-borne) typhus', 'Kedani fever', 'typhus fever due to Rickettsia tsutsugamushi', 'tsutsugamushi', 'chigger-borne rickettsiosis', 'tropical typhus', 'Mite-borne rickettsiosis', 'tsutsugamushi fever', 'tsutsugamushi disease']",13371,,83317,C0036472,,,0007480,D012612,081.2,,10039766,
mondo:0019366,free sialic acid storage disease,,,,834,CN206051,"['-0.1552', '0.4539', '-0.1169', '0.2937', '0.3198', '-0.608', '-0.3533', '0.1432', '-0.7563', '0.1021', '-0.555', '0.02797', '0.09326', '-0.06635', '0.11566', '-0.295', '-0.1273', '-0.3416', '-0.5586', '-0.4304', '-0.05792', '-0.4158', '0.717', '-0.471', '-0.01215', '-0.2157', '-0.2108', '0.1638', '-0.4333', '0.347', '0.5977', '0.02014', '0.2888', '0.2439', '0.2499', '-0.1085', '-0.5', '-0.1492', '-0.1844', '0.0685', '-0.3208', '-0.917', '0.1709', '-0.05756', '-0.2004', '-0.04135', '0.02972', '0.2295', '-0.3115', '0.2343', '-0.02008', '0.4795', '-0.1279', '-0.2617', '0.323', '-0.6924', '0.1072', '-0.033', '0.01152', '0.04938', '0.2627', '-0.001567', '0.2205', '-0.03427', '0.3196', '0.1654', '0.447', '-0.3823', '-0.7124', '-0.05475', '-0.0203', '-0.12134', '0.1481', '0.1598', '0.2426', '0.1094', '0.0317', '-0.1631', '-0.4272', '-0.279', '-0.0147', '-0.07806', '-0.349', '0.463', '0.1364', '0.0772', '-0.2764', '0.04785', '0.6084', '-0.1098', '0.5283', '0.292', '-0.03442', '-0.2158', '0.3828', '0.3604', '0.4114', '-0.304', '0.3284', '0.05707']",,,C538523,,,10067531,
mondo:0019367,regional odontodysplasia,['ghost teeth'],,,83450,,,,,D018126,,,,
mondo:0019368,florid cemento-osseous dysplasia,"['focal cemento-osseous dysplasia', 'florid osseous dysplasia', 'Gigantiform cementoma']",,,83451,C0555197,,C8381,,C537063,,D16.5,,
mondo:0019369,complex regional pain syndrome,"['CRPS', 'Complex regional pain syndromes', 'reflex sympathetic dystrophy']",3223,,83452,C0458219,,,,D020918,,,10064332,
mondo:0019370,vulvovaginal gingival syndrome,,,,83453,CN206058,,,,,,,,
mondo:0019371,narcolepsy without cataplexy,,,,83465,CN206062,,,0005855,,347.00,G47.419,,
mondo:0019372,solitary bone cyst,"['cyst of bone', 'bone cyst', 'unicameral bone cyst', 'simple bone cyst', 'cyst of the bone', 'solitary cyst']",,,83468,,,C2904,,D001845,733.21,M85.4,,
mondo:0019373,desmoplastic small round cell tumor,"['Desmoplastic small round cell tumor', 'Desmoplastic small round-cell tumour', 'Desmoplastic small round-cell tumor', 'Polyphenotypic small round cell tumor', 'desmoplastic small round cell tumor', 'Desmoplastic small round cell tumour', 'desmoplastic small-round-cell tumor', 'DSRCT', 'Polyphenotypic small round cell tumour', 'Desmoplastic small round-cell neoplasm', 'Desmoplas. small round cell tumour', 'desmoplastic small-round-cell tumour', 'Desmoplas. small round cell tumor']",6785,,83469,C0281508,,C8300,1000895,D058405,,,10064587,
mondo:0019374,CAMOS syndrome,"['CAMOS', 'spinocerebellar ataxia autosomal recessive 5', 'cerebellar ataxia with mental retardation optic atrophy and skin abnormalities', 'SCAR5', 'cerebellar ataxia-intellectual disability-optic atrophy-skin abnormalities syndrome', 'cerebellar ataxia with intellectual disability optic atrophy and skin abnormalities']",,606937,83472,C4511633,,,,,,,,
mondo:0019375,megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome,"['megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome', 'MPPH syndrome', 'megalencephaly, polymicrogyria, and hydrocephalus (MPPH) syndrome', 'megalencephaly and perisylvian polymicrogyria with postaxial polydactyly and hydrocephalus']",,,83473,,"['0.0181', '-0.1486', '0.1459', '0.389', '-0.3364', '-0.2249', '-0.1213', '0.567', '-0.3176', '0.3315', '-0.2668', '-0.9116', '-0.174', '0.1947', '0.372', '0.0807', '-0.1995', '0.0238', '-0.6904', '-1.135', '0.001723', '-0.0557', '0.3557', '-0.4678', '-0.1954', '-0.542', '-1.072', '0.7524', '-0.2479', '0.2705', '-0.1833', '-0.908', '0.466', '-0.338', '-0.2217', '0.6143', '-0.000935', '0.1816', '-0.03223', '-0.0886', '0.924', '0.3772', '-0.0258', '-0.789', '1.027', '-0.12164', '0.601', '-0.532', '0.252', '0.2357', '0.3875', '0.02936', '-0.1312', '-1.144', '0.1642', '-0.2408', '-0.0769', '0.08777', '0.169', '0.534', '-0.271', '0.509', '-0.5674', '-0.1423', '-0.03928', '0.1534', '0.1152', '0.1284', '-0.8804', '0.1788', '-0.2384', '1.113', '0.2893', '-0.8086', '0.12286', '0.4487', '0.3945', '0.729', '-0.2903', '-0.821', '-0.3447', '-0.1609', '-0.2864', '0.5894', '0.512', '0.9526', '0.4224', '0.1558', '0.1615', '-0.357', '-0.2136', '1.008', '0.4019', '0.2903', '0.9043', '0.361', '0.57', '-0.439', '0.0341', '0.1661']",,,,,,,
mondo:0019376,West-Nile encephalitis,"['West Nile fever encephalitis', 'West Nile encephalitis', 'West Nile virus caused infectious encephalitis', 'West-Nile fever', 'West Nile fever with encephalitis']",2365,,83476,,,,0007545,D014901,066.41,,,
mondo:0019377,Mycoplasma encephalitis,['Mycoplasma pneumoniae caused infectious encephalitis'],,,83482,,,,,,,,,
mondo:0019378,la Crosse encephalitis,"['California encephalitis', 'Californian encephalitis', 'La Crosse virus caused infectious encephalitis', 'California virus encephalitis', 'Neuroinvasive California encephalitis virus infection']",0050118,,83483,C0276379,,,,D004670,062.5,,10014584,
mondo:0019380,western equine encephalitis,"['Western equine encephalomyelitis', 'WEE', 'Western equine encephalitis virus caused infectious encephalitis']",10843,,83593,C0153064,,C85227,0007546,D020241,062.1,A83.1,10014614,
mondo:0019383,acute disseminated encephalomyelitis,"['acute disseminated encephalomyelitis', 'ADEM', 'ADE', 'acute disseminated encephalitis']",639,,83597,C0014059,,C34578,0007130,D004673,136.9,,,
mondo:0019384,encephalitis lethargica,"['Von Economo’s disease', 'encephalitis lethargica', 'lethargic encephalitis', 'von Economo disease', 'epidemic encephalitis', 'von Economo^s disease', 'Von Economo encephalitis']",5225,,83600,C0014040,,C34576,,,049.8,,10052369,
mondo:0019385,steroid-responsive encephalopathy associated with autoimmune thyroiditis,"['Hashimoto^s encephalopathy', 'steroid-responsive encephalopathy associated with thyroid disease', 'Hashimoto^s encephalitis', 'Hashimoto encephalitis', 'SREAT']",,,83601,C0393639,,,,C535841,,,,
mondo:0019386,progressive rubella panencephalitis,,,,83616,C1305924,,,,,,,,
mondo:0019387,macrostomia-preauricular tags-external ophthalmoplegia syndrome,,,,83619,CN206081,,,,,,,,
mondo:0019388,pelvis syndrome,"['LUMBAR syndrome', 'SACRAL syndrome', 'Lower body hemangioma-urogenital anomalies-myelopathy-bony deformities-anorectal and arterial malformations-renal anomalies syndrome', 'urorectal septum malformation sequence', 'perineal hemangioma-external genitalia malformations-lipomyelomeningocele-vesicorenal abnormalities-imperforate anus syndrome']",,,83628,CN206083,,,,,,,,
mondo:0019390,Susac syndrome,"['RED-M', 'retinopathy-encephalopathy-deafness associated with microangiopathy', 'Retinocochleocerebral vasculopathy', 'SICRET (small infarction of cochlear, retinal, and encephalic tissue) syndrome', 'small infarctions of cochlear, retinal and encephalic tissue', 'SICRET syndrome']",,,838,C2717757,,C116363,1001856,D055955,348.39,,10071573,
mondo:0019391,Fanconi anemia,"['Fanconi^s anemia', 'Fanconi panmyelopathy', 'Panmyelopathy, Fanconi', 'Fanconi pancytopenia', 'pancytopenia, congenital', 'primary erythroid hypoplasia', 'Fanconi^s anaemia']",13636,,84,C0015625,"['0.0623', '0.3604', '-0.2542', '0.001464', '0.6196', '0.152', '0.0286', '0.696', '-0.4932', '-0.537', '0.467', '0.161', '0.3816', '0.3257', '-0.922', '-0.224', '-0.5903', '0.00881', '-0.2236', '-0.05856', '-0.02205', '-0.3945', '0.5493', '-0.2346', '0.4082', '-0.2944', '0.01976', '-0.2776', '0.373', '0.1779', '0.06647', '-0.0001361', '0.485', '0.3765', '0.4597', '-0.393', '-0.4734', '-0.596', '0.05066', '-0.007294', '-0.1614', '0.6865', '0.2202', '-0.4924', '-0.1885', '-0.6284', '-0.143', '0.1779', '0.3442', '-0.4297', '0.10736', '0.4102', '0.6436', '-0.2073', '0.5205', '-0.188', '-0.208', '0.1416', '-0.6753', '-0.1335', '-0.1499', '0.1527', '-0.29', '-0.03165', '0.3044', '0.1674', '0.4585', '0.71', '-0.02168', '1.004', '0.658', '-0.4138', '-0.3582', '-0.33', '0.4368', '0.1858', '0.0975', '-0.203', '-0.1243', '-0.10614', '0.10864', '0.1074', '0.331', '0.0525', '0.1821', '-0.3323', '-0.488', '0.2522', '0.2888', '-0.3604', '0.664', '0.4656', '-0.4277', '0.0952', '0.5425', '0.0994', '0.3958', '0.1201', '0.6455', '-0.11414']",C62505,,D005199,284.09,,10055206,
mondo:0019392,syringocystadenoma papilliferum,"['papillary Syringadenoma', 'naevus syringocystadenomatosus papilliferus', 'Syringadenoma', 'fistulous vegetative verrucous hydradenoma', 'Syringadenoma papilliferum', 'papillary Syringadenoma (syringocystadenoma papilliferum)', 'papillary syringadenoma (morphologic abnormality)', 'syringocystadenoma papilliferum', 'SCAP', 'papillary syringocystadenoma']",5445,,840,C0406803,,C4172,1000558,,,,10042926,
mondo:0019393,idiopathic malabsorption due to bile acid synthesis defects,['idiopathic bile acid malabsorption'],,,84065,,,,,,,,,
mondo:0019394,Senior-Boichis syndrome,"['nephronophthisis-hepatic fibrosis syndrome', 'Boichis disease']",,,84081,CN206093,"['-0.02081', '-0.1826', '-0.02963', '0.4177', '-0.04343', '-0.662', '-0.2455', '0.456', '0.02054', '-0.3428', '-0.3857', '-0.3147', '0.1154', '0.273', '-0.1216', '-0.3396', '-0.1455', '-0.06445', '0.1511', '-0.5874', '0.327', '-0.1284', '0.05084', '-0.389', '0.571', '-0.1432', '-0.1592', '0.2524', '0.08936', '-0.2064', '0.696', '-0.749', '0.1351', '0.11646', '0.08704', '-0.1182', '-0.3687', '-0.2213', '-0.5527', '0.2976', '-0.1148', '0.1473', '0.2328', '-0.1497', '0.2135', '-0.07074', '0.2047', '-0.3906', '-1.002', '-0.619', '-0.288', '0.4397', '0.1156', '0.0985', '0.256', '-0.689', '0.0905', '0.1775', '-0.899', '0.335', '0.1447', '-0.299', '0.05487', '0.165', '0.05402', '-0.2211', '0.8057', '0.618', '-0.8545', '-0.02377', '-0.476', '0.2032', '0.0733', '-0.0262', '0.1786', '0.002913', '0.2211', '-0.02574', '0.014305', '0.08356', '0.233', '0.5083', '-0.04562', '0.2747', '0.02756', '-0.4546', '0.6235', '0.502', '0.2854', '-0.5073', '0.3848', '0.1544', '-0.05508', '-0.1686', '0.6675', '0.0769', '0.01727', '-0.3691', '0.1647', '-0.0333']",,,,,,,
mondo:0019395,Hinman syndrome,"['occult neuropathic bladder', 'non-neurogenic neurogenic bladder', 'HAS', 'Hinman-Allen syndrome', 'HS']",,,84085,CN206094,,,,,596.59,,,
mondo:0019396,collagen type III glomerulopathy,['Collagenofibrotic glomerulopathy'],,,84087,CN206095,,,,,583.89,,,
mondo:0019397,unknown leukodystrophy,,,,84096,,,,,,,,,
mondo:0019398,desmin-related myopathy with Mallory body-like inclusions,['early-onset desmin-related myopathy'],,,84132,,"['-0.12415', '0.1285', '-0.012474', '-0.03702', '0.03506', '-0.1777', '0.01187', '0.1451', '-0.12067', '-0.02765', '-0.05188', '-0.04074', '-0.0089', '0.02383', '0.001466', '-0.0275', '-0.00989', '0.01167', '-0.105', '-0.259', '0.03232', '-0.07837', '0.09204', '-0.01015', '0.03653', '-0.02692', '-0.07117', '-0.04123', '-0.003159', '-0.05298', '0.1019', '0.0451', '0.1543', '0.0552', '0.0704', '-0.06433', '-0.0791', '-0.1462', '0.03183', '-0.1675', '-0.001422', '-0.1545', '0.0297', '-0.03265', '-0.03818', '-0.0892', '-0.0454', '0.0931', '-0.0005364', '0.02365', '-0.0465', '0.0282', '0.03845', '-0.005856', '-0.0837', '-0.0922', '0.1389', '-0.06323', '-0.1501', '0.0328', '0.129', '0.05502', '0.00393', '-0.0252', '-0.0627', '-0.01624', '0.1656', '0.1164', '-0.1443', '0.127', '-0.11163', '-0.02882', '0.0137', '-0.0729', '0.03918', '0.0391', '-0.00925', '0.02132', '-0.05328', '-0.03638', '0.04', '-0.01631', '-0.000879', '0.1547', '-0.02426', '0.00841', '0.0221', '0.1597', '0.1096', '0.001351', '0.1736', '0.05984', '-0.006237', '0.04526', '0.2776', '0.131', '0.1376', '-0.1627', '-0.01898', '0.0334']",,,,,,,
mondo:0019399,Isaac syndrome,"['continuous muscle fibre activity syndrome', 'Isaac^s-Merten^s syndrome', 'Isaacs^ syndrome', 'continuous muscle fiber activity syndrome', 'neuromyotonia', 'peripheral nerve hyperexcitability', 'Isaac-Mertens syndrome', 'Quantal squander syndrome', 'acquired neuromyotonia']",,,84142,CN206101,,,,,,,,
mondo:0019401,sporadic idiopathic steroid-resistant nephrotic syndrome,['sporadic idiopathic nephrosis'],,,84271,C4274017,,,,,,,,
mondo:0019402,beta thalassemia,"['Beta thalassemia minor', 'erythroblastic anaemia', 'thalassemia major', 'erythroblastic anemia', 'Thalassemias, beta-', 'Beta thalassemia intermedia', 'thalassemia, Hispanic gamma-delta-beta']",12241,,848,,"['-0.231', '0.1111', '-0.356', '-0.3765', '-0.2119', '-0.3389', '-0.655', '1.269', '-0.8213', '-0.7803', '-0.5083', '0.06198', '0.415', '0.6323', '-0.1816', '-0.4392', '-1.469', '-0.3877', '-0.787', '-0.7944', '-0.6367', '-0.342', '1.087', '-0.4878', '0.726', '0.19', '0.4507', '-0.1793', '0.2407', '-0.578', '0.2429', '0.1082', '-0.2435', '-0.5654', '-0.4497', '-0.716', '-0.5513', '-0.363', '-0.1418', '-0.6235', '0.2015', '0.1259', '0.5894', '-0.4595', '-0.4868', '-0.497', '-0.862', '-0.7476', '0.0799', '-0.773', '0.2888', '-0.9116', '0.4382', '0.02252', '0.0697', '0.04584', '-0.2583', '0.8115', '-0.1147', '0.3088', '-0.3623', '0.1434', '-0.05133', '-0.5557', '-0.0821', '0.05347', '0.2517', '0.1844', '-1.097', '0.5664', '0.0276', '0.2021', '-0.1855', '-0.1389', '0.6055', '0.3315', '-0.079', '-0.02069', '0.06134', '-0.0505', '-0.3403', '-0.5635', '-0.0895', '-0.2063', '-0.2654', '0.1549', '0.523', '0.3564', '0.04703', '0.3901', '0.3904', '-0.006847', '-0.3792', '-0.4678', '0.2903', '0.02295', '-0.5864', '-0.08215', '-0.1097', '-0.675']",C34375,,D017086,282.49,,10043391,
mondo:0019403,congenital dyserythropoietic anemia,"['anemia, congenital dyserythropoietic', 'congenital dyshaematopoietic anemia', 'dyserythropoietic anemia, congenital', 'congenital dyshaematopoietic anaemia', 'CDA']",1338,,85,C0002876,"['-0.456', '0.2039', '-0.1665', '0.4587', '0.2644', '0.3909', '-0.2054', '0.6963', '0.04224', '-0.5073', '0.526', '-0.02312', '0.5063', '0.00895', '-1.182', '0.07', '-0.874', '0.01929', '-0.2786', '-0.4453', '-0.235', '-0.2693', '0.6475', '0.00535', '0.626', '-0.1467', '0.010315', '-0.3489', '0.4094', '0.3047', '0.302', '0.02397', '0.5747', '0.5127', '0.382', '-0.3997', '-0.7695', '-0.824', '0.5176', '-0.1344', '-0.6562', '0.2993', '0.1475', '-0.4497', '-0.4944', '-0.7', '0.02159', '0.4114', '-0.0521', '-0.3115', '0.4275', '0.4204', '0.716', '-0.2898', '0.6035', '-0.6997', '0.01617', '0.1271', '-0.912', '0.043', '0.0009694', '0.2136', '-0.01031', '-0.1931', '-0.06854', '0.1261', '0.2448', '0.832', '-0.3372', '0.75', '0.8623', '-0.3528', '-0.3813', '-0.4517', '0.302', '0.9844', '0.1884', '0.173', '0.1498', '0.512', '0.0963', '0.0831', '-0.05057', '-0.0926', '0.3757', '-0.3977', '-0.321', '0.5444', '0.82', '-0.4468', '0.6777', '0.3735', '-0.2615', '0.2927', '0.742', '1.076', '0.3547', '0.2861', '0.3997', '-0.6934']",C84646,,D000742,285.8,D64.4,,
mondo:0019404,perineurioma,"['soft tissue perineurioma', 'perineurioma']",4697,,85102,C0751691,,C4973,,,215.9,,,
mondo:0019405,facial onset sensory and motor neuronopathy,"['facial onset sensory and motor neuronopathy syndrome', 'FOSMN syndrome', 'facial onset sensorimotor neuronopathy syndrome']",,,85162,CN206118,,,,,,,,
mondo:0019406,craniofacial conodysplasia,,,,85168,,,,,,,,,
mondo:0019407,"microcephalic osteodysplastic dysplasia, Saul-Wilson type","['microcephalic osteodysplastic dysplasia, Saul-Wilson type', 'Saul-Wilson syndrome', 'microcephalic osteodysplastic dysplasia', 'SWILS']",0111673,618150,85172,,"['-0.5215', '0.1863', '0.4045', '-0.2472', '0.202', '-0.1791', '-0.1952', '0.857', '-0.623', '-0.2338', '-0.1881', '-0.1674', '0.01595', '0.03207', '0.2656', '0.3386', '0.3474', '-0.11957', '-0.2223', '-0.5', '0.1654', '0.08765', '0.3118', '-0.2546', '0.1569', '-0.0799', '-0.2988', '-0.01741', '0.2249', '-0.1145', '0.3406', '-0.1624', '0.2683', '0.05148', '0.402', '-0.09296', '-0.01689', '-0.459', '-0.1415', '-0.3862', '0.427', '-0.01361', '-0.07996', '-0.1345', '0.01364', '-0.2284', '0.12054', '0.355', '-0.03366', '-0.332', '-0.02097', '-0.0577', '-0.2241', '0.6626', '-0.2347', '-0.695', '-0.273', '-0.02127', '0.014366', '0.3098', '0.1687', '-0.2369', '-0.279', '0.1881', '-0.2152', '0.114', '0.0797', '0.2656', '-0.3608', '0.3965', '-0.2642', '0.006886', '0.4543', '-0.1365', '-0.3125', '0.2365', '-0.1925', '0.128', '-0.3325', '-0.1874', '0.07513', '0.03015', '-0.269', '0.4043', '-0.1583', '0.2634', '0.0696', '0.5845', '0.5156', '0.4116', '-0.194', '0.2986', '-0.0324', '-0.02084', '0.4795', '-0.0143', '0.10443', '-0.2073', '0.4863', '0.0903']",,,,,,,
mondo:0019408,Astley-Kendall dysplasia,"['short limbed dwarfism with extensive stippling', 'Astley-Kendall syndrome']",,,85175,C1300228,,,,C535392,,,,
mondo:0019409,idiopathic juvenile osteoporosis,"['juvenile osteoporosis', 'idiopathic juvenile osteoporosis', 'Paediatric osteoporosis', 'Ijo', 'Pediatric osteoporosis', 'osteoporosis, juvenile', 'idiopathic osteoporosis']",12559,615221,85193,CN536248,"['0.3994', '-0.3533', '-0.05255', '0.6655', '0.0934', '-0.5376', '-0.4138', '0.803', '-0.648', '-0.4124', '0.2002', '0.3938', '-0.142', '0.3608', '-0.1246', '-0.1368', '-0.1318', '0.4746', '-0.8086', '-0.2505', '-0.0999', '-0.3474', '0.253', '-0.5117', '0.2472', '-0.334', '0.234', '-0.7065', '-0.6113', '-0.107', '0.553', '-0.575', '-0.2496', '-0.2683', '0.02199', '-0.3162', '0.006943', '-0.6626', '-0.01962', '-0.4053', '0.2273', '-0.1305', '0.3372', '-0.561', '0.7993', '-0.2883', '0.0633', '0.1918', '0.1', '0.5894', '0.6255', '0.04276', '0.2832', '-0.05273', '-0.421', '-0.548', '-0.2856', '0.1718', '-0.4055', '-0.254', '0.2493', '0.2079', '-0.7676', '-0.5923', '0.03244', '0.814', '0.2612', '0.627', '-0.2391', '-0.4885', '0.6616', '-0.1249', '0.06018', '-0.4397', '0.2197', '0.798', '-0.3452', '0.524', '-0.1896', '0.0756', '0.094', '-0.4336', '0.2026', '0.513', '-0.4966', '0.7656', '0.33', '0.01483', '1.1875', '0.0535', '-0.351', '-0.3323', '-0.918', '-0.1533', '0.545', '-0.342', '0.11395', '-0.4814', '-0.2257', '-0.6055']",C119996,,C537700,733.02,,,
mondo:0019411,genochondromatosis type 1,,,,85197,,,,,,,,,
mondo:0019412,dysspondyloenchondromatosis,,,,85198,C4302548,,,,,,,,
mondo:0019413,ischio-vertebral syndrome,"['ischio-spinal dysostosis', 'ischio-vertebral dysplasia']",,,85200,CN206143,,,,,,,,
mondo:0019414,BRESEK syndrome,['BRESHECK syndrome'],,,85284,C3502469,"['-0.1488', '0.1857', '0.5015', '-0.4048', '0.5464', '-0.2793', '-0.791', '0.713', '-0.3772', '-0.526', '-0.05817', '-0.2052', '0.2325', '0.2576', '-0.2913', '0.12476', '0.4397', '-0.2998', '-0.6045', '-0.3447', '0.2046', '-0.2043', '0.4382', '-0.5513', '0.01198', '-0.2961', '-0.549', '0.1418', '0.3762', '-0.5737', '0.1582', '-0.2285', '0.04364', '0.1031', '-0.0578', '-0.243', '0.2017', '-0.4875', '-0.265', '0.05057', '-0.285', '0.1047', '-0.05823', '-0.3887', '-0.2494', '-0.436', '-0.2021', '0.1024', '-0.5024', '-0.4592', '0.01207', '0.004707', '-0.04126', '-0.1565', '-0.2263', '-0.8574', '-0.1073', '0.3196', '-0.1519', '0.268', '-0.1282', '-0.2732', '-0.31', '0.4077', '-0.792', '-0.0708', '0.4949', '0.5483', '-0.9575', '0.2717', '-0.3696', '0.03183', '0.4229', '-0.09076', '0.04163', '0.1675', '-0.432', '0.3433', '-0.3652', '0.005135', '-0.303', '0.1793', '0.2534', '0.5835', '-0.1959', '-0.10376', '0.4968', '0.5215', '0.0885', '0.1378', '0.06204', '0.564', '0.507', '0.1584', '0.6167', '-0.03973', '-0.04544', '-0.322', '0.4185', '0.1877']",,,C564519,,,,
mondo:0019415,fetal and neonatal alloimmune thrombocytopenia,['NAIT'],,,853,,,,,,,P61.0,,
mondo:0019416,X-linked intellectual disability-hypogammaglobulinemia-progressive neurological deterioration syndrome,,,,85317,CN206172,,,,,,,,
mondo:0019417,X-linked intellectual disability-precocious puberty-obesity syndrome,,,,85318,CN227629,,,,,,,,
mondo:0019418,X-linked intellectual disability-epilepsy-progressive joint contractures-dysmorphism syndrome,,,,85319,CN206173,,,,,,,,
mondo:0019419,X-linked intellectual disability-macrocephaly-macroorchidism syndrome,['Johnson syndrome'],,,85320,CN206174,,,,,,,,
mondo:0019420,"X-linked intellectual disability, Pai type",,,,85322,CN206176,,,,,,,,
mondo:0019421,"X-linked intellectual disability, Seemanova type",,,,85323,CN227630,,,,,,,,
mondo:0019422,"X-linked intellectual disability, Stevenson type",,,,85325,CN206178,,,,,,,,
mondo:0019423,"X-linked intellectual disability, Stoll type",,,,85326,CN206179,,,,,,,,
mondo:0019424,X-linked intellectual disability-acromegaly-hyperactivity syndrome,,,,85327,CN227631,,,,,,,,
mondo:0019426,X-linked intellectual disability-corpus callosum agenesis-spastic quadriparesis syndrome,['X-linked intellectual disability - corpus callosum agenesis - spastic quadriparesis'],,,85330,CN206182,,,,,,,,
mondo:0019427,"X-linked neurodegenerative syndrome, Bertini type",,,,85334,CN206185,,,,,,,,
mondo:0019428,fried syndrome,,,,85335,CN206186,,,,,,,,
mondo:0019429,"X-linked neurodegenerative syndrome, Hamel type",,,,85336,CN206187,,,,,,,,
mondo:0019430,X-linked intellectual disability-ataxia-apraxia syndrome,,,,85338,CN227633,,,,,,,,
mondo:0019431,primitive portal vein thrombosis,['non-cirrhotic portal vein thrombosis'],,,854,C0155773,,,,,,I81,10036206,
mondo:0019432,rheumatoid factor-negative juvenile idiopathic arthritis,"['polyarthritis without rheumatoid factor', 'rheumatoid factor-negative JIA', 'juvenile rheumatoid factor-negative polyarthritis']",,,85408,,,,,,,,,
mondo:0019433,oligoarticular juvenile idiopathic arthritis,"['Pauciarticular JIA', 'Pauciarticular juvenile idiopathic arthritis', 'Oligoarticular JIA', 'Pauciarticular chronic arthritis']",,,85410,C3898105,,C119032,1002019,C536312,,M08.4,,
mondo:0019434,systemic-onset juvenile idiopathic arthritis,"['systemic onset juvenile rheumatoid arthritis', 'systemic juvenile idiopathic arthritis', 'Still^s disease (formerly)', 'SoJIA', 'systemic polyarthritis', 'systemic-onset JIA', 'sJIA', 'systemic onset juvenile idiopathic arthritis', 'Still disease']",,,85414,,"['0.457', '0.4583', '-0.696', '0.349', '0.03442', '-0.442', '0.10364', '0.574', '-0.922', '-0.408', '-0.3093', '0.2404', '0.09717', '0.769', '-0.2448', '0.04947', '-0.652', '0.357', '0.298', '-0.5117', '-0.1321', '-0.152', '0.7046', '-0.866', '0.02579', '0.6084', '-0.0914', '0.1216', '-0.2693', '0.247', '0.548', '-0.4219', '0.4792', '0.4163', '0.02452', '-0.1936', '-0.912', '0.1378', '-0.0825', '0.1417', '0.2683', '0.3496', '0.06915', '-0.378', '0.4502', '0.5513', '-0.4062', '-0.1715', '0.0782', '0.2654', '-0.3833', '0.303', '0.3801', '0.565', '0.3877', '-0.05502', '-0.5996', '-0.2163', '-1.285', '-0.3125', '-0.2515', '0.398', '-0.4075', '0.3618', '0.8267', '0.2124', '0.1635', '0.612', '0.3843', '0.4067', '-0.271', '-0.3616', '-0.2345', '-0.5493', '0.0346', '0.834', '-0.05966', '0.4668', '0.1058', '-0.2627', '0.1023', '-0.1968', '-0.1749', '0.418', '-0.1603', '-0.3154', '0.10596', '0.2047', '-0.3486', '0.6587', '0.2715', '-0.1309', '-0.2208', '0.2568', '0.4106', '0.162', '0.3857', '-0.541', '-0.02466', '-0.471']",C119031,1001999,C565798,,,,
mondo:0019435,rheumatoid factor-positive polyarticular juvenile idiopathic arthritis,"['polyarthritis with rheumatoid factor', 'polyarticular juvenile idiopathic arthritis, RF+', 'rheumatoid factor-positive polyarticular JIA', 'polyarticular JIA, RF+', 'juvenile idiopathic rheumatoid factor-positive polyarthritis', 'polyarticular juvenile idiopathic arthritis, rheumatoid Factor Positive']",,,85435,C3890733,,C119034,,,,,,
mondo:0019436,psoriasis-related juvenile idiopathic arthritis,"['psoriasis-related JIA', 'juvenile psoriatic arthritis', 'JPsA']",,,85436,,,C114361,,,,,,
mondo:0019437,enthesitis-related juvenile idiopathic arthritis,"['era', 'enthesitis related arthritis, juvenile', 'juvenile spondylarthropathy', 'juvenile enthesitis-related arthritis', 'enthesitis-related JIA', 'enthesitis-related arthritis']",,,85438,,,C119024,,,,,,
mondo:0019438,AL amyloidosis,"['amyloidosis primary systemic', 'amyloidosis AL', 'primary systemic AL amyloidosis', 'primary amyloidosis (formerly)', 'systemic AL amyloidsis', 'Light-chain amyloidosis', 'Light chain amyloidosis', 'primary AL amyloidosis', 'primary systemic amyloidosis', 'primary amyloidosis']",0080933,,85443,C0268381,,C158963,,C531616,,,10036673,
mondo:0019439,AA amyloidosis,"['inflammatory amyloidosis', 'reactive amyloidosis', 'amyloid A amyloidosis', 'secondary amyloidosis', 'amyloidosis AA']",0080936,,85445,C3536715,,C3818,,,277.39,,10039811,
mondo:0019440,wild type ABeta2M amyloidosis,"['amyloidosis beta2m', 'dialysis-related arthropathy', 'ABeta2Mwt amyloidosis', 'amyloidosis dialysis-related', 'DRA', 'Beta-2-microglobulin amyloidosis', 'wild type ABeta2-microglobulinic amyloidosis', 'dialysis-related amyloidosis']",,,85446,CN206197,,,,,,,,
mondo:0019441,ATTRV122I amyloidosis,"['ATTR cardiomyopathy', 'ATTRV122I-related amyloidosis', 'transthyretin-related familial amyloid cardiomyopathy', 'TTR-related amyloid cardiomyopathy', 'TTR-related cardiac amyloidosis', 'transthyretin amyloid cardiopathy']",,,85451,,"['0.4634', '-0.582', '-0.7124', '0.1582', '0.2678', '-0.2722', '-0.4167', '0.2803', '-0.8286', '-0.1114', '-0.1908', '0.12427', '-0.9204', '0.10504', '-0.711', '-0.191', '0.0384', '-0.8066', '0.0844', '-0.599', '0.5103', '-0.1586', '0.8574', '0.0817', '0.1991', '0.6973', '-0.5576', '-0.0325', '0.3713', '0.319', '0.3145', '-0.3079', '0.939', '-0.7075', '0.277', '-1.032', '-0.3193', '0.0675', '0.3145', '0.10254', '0.1246', '0.09076', '0.0135', '0.5513', '0.3818', '-0.5273', '-0.7715', '0.0252', '-0.06067', '0.7725', '-0.04547', '0.366', '0.4268', '-0.1332', '-0.3157', '-0.2515', '0.6865', '0.08514', '-0.257', '-0.7217', '-0.2233', '0.3442', '0.6157', '-0.78', '0.04187', '-0.604', '0.491', '0.9375', '-0.79', '0.4473', '-0.5464', '0.136', '-0.435', '0.0986', '0.5767', '0.7188', '-0.4177', '1.027', '-0.4478', '-0.679', '-0.0774', '-0.3596', '0.2886', '0.02147', '0.1311', '-0.3923', '-0.02545', '-0.1403', '-0.02957', '-0.02618', '0.4827', '-0.3909', '-0.501', '-0.2603', '0.7275', '0.25', '-0.4717', '-0.3296', '0.1455', '-0.005478']",,,,,,,
mondo:0019443,dextro-looped transposition of the great arteries,"['ventriculoarterial discordance with atrioventricular concordance', 'congenitally uncorrected transposition of the great vessels', 'D-TGA', 'isolated ventriculoarterial discordance', 'congenitally uncorrected transposition of the great arteries', 'DTGA']",0060770,,860,,"['0.1327', '-0.2416', '-0.4966', '0.412', '0.6406', '-0.6553', '0.1141', '0.5806', '-0.3113', '-0.582', '-0.1214', '-0.3594', '0.03226', '0.929', '-0.885', '-0.86', '-1.246', '-0.0632', '-0.2294', '-0.778', '-0.0737', '0.569', '0.2805', '-0.10144', '-0.1526', '-0.503', '0.5215', '0.7036', '0.6245', '0.1881', '1.133', '-0.2803', '0.215', '0.2727', '0.0938', '0.0601', '0.2231', '0.3264', '0.587', '-0.2427', '0.5337', '0.548', '0.2705', '0.2113', '0.0009365', '0.1376', '0.007324', '-0.2076', '-0.1265', '-0.0381', '-0.201', '-0.503', '0.424', '-0.3354', '-0.3376', '0.2556', '-0.5347', '0.4807', '-0.2996', '0.1501', '-0.3616', '0.4558', '0.2097', '0.1772', '-0.1749', '-0.01192', '0.8604', '0.3342', '-0.4607', '0.463', '-0.0436', '0.3726', '0.4253', '-0.4585', '-0.328', '0.7646', '0.6533', '-0.5483', '-0.766', '-0.0798', '0.2026', '-0.467', '0.2776', '-0.1536', '0.47', '-0.2451', '-0.02834', '0.2148', '-0.05673', '-0.1562', '0.7227', '0.02147', '0.1582', '0.11475', '0.4797', '-0.2281', '-0.04877', '-0.507', '-0.1826', '0.0864']",,,,,,,
mondo:0019444,trichinellosis,"['infection with Trichinella', 'Human trichinellosis', 'Trichinella caused disease or disorder', 'trichinosis', 'Trichinella spiralis infection', 'trichiniasis']",9784,,863,,,C85199,0007520,D014235,124,B75,10044608,
mondo:0019445,trichofolliculoma,,,,864,C0334262,,C4112,,C536553,,,10044611,
mondo:0019446,localized lichen myxedematosus,['papular mucinosis'],,,86795,C0263390,,,,,,,,
mondo:0019447,atypical lichen myxedematosus,['Intermediate lichen myxedematosus'],,,86797,C4510874,,,,,,,,
mondo:0019448,benign adult familial myoclonic epilepsy,"['familial cortical myoclonic tremor and epilepsy', 'BAFME', 'ADCME', 'benign adult familial myoclonus epilepsy', 'familial adult myoclonic epilepsy', 'FAME', 'autosomal dominant cortical myoclonus and epilepsy', 'FCMTE']",,,86814,CN206220,"['0.9316', '0.251', '-0.4988', '-0.0696', '-0.442', '-0.4092', '0.672', '0.683', '-0.4072', '-0.4353', '-0.04788', '-0.1599', '-0.4883', '0.1925', '0.2747', '0.04712', '-0.3318', '-0.6367', '-0.1973', '-0.6587', '-0.3008', '0.551', '0.02603', '-0.3442', '-0.4006', '0.03656', '-0.1812', '-0.3694', '-0.3835', '0.1233', '0.267', '-0.5586', '0.10126', '0.0241', '0.671', '0.1641', '0.0946', '0.1367', '-0.1207', '-0.2096', '-0.1774', '-0.3655', '0.08936', '-0.3674', '-0.1184', '-0.8438', '-0.1646', '0.197', '0.4153', '0.347', '0.01755', '0.1863', '0.1666', '-0.5146', '0.1888', '-0.007416', '0.0326', '-0.03772', '-0.0632', '0.0588', '-0.5845', '0.583', '0.737', '-0.4119', '-0.6094', '1.136', '0.2812', '0.05624', '-0.7354', '0.6357', '0.8057', '0.6094', '0.0244', '-0.535', '0.08734', '0.665', '1.013', '0.1887', '-0.167', '0.3257', '-0.049', '0.7104', '0.484', '0.1849', '0.1517', '0.2903', '0.09344', '0.4226', '0.645', '0.2837', '0.02075', '-0.01164', '-0.2023', '0.04318', '-0.09033', '0.0955', '0.4019', '-0.314', '0.419', '0.2498']",,,,,,,
mondo:0019449,lissencephaly type 3-familial fetal akinesia sequence syndrome,,,,86821,CN227635,,,,,,,,
mondo:0019450,lissencephaly with cerebellar hypoplasia,['LCH'],,,86823,C4274995,"['0.07184', '0.1874', '0.07666', '-0.2115', '0.2893', '-0.3489', '0.2795', '0.554', '-0.384', '-0.0673', '-0.69', '-0.0611', '-0.4255', '-0.01259', '0.525', '0.1781', '0.2069', '-0.7837', '0.46', '-0.3303', '-0.055', '0.1206', '0.6187', '-0.5483', '0.6494', '-0.03473', '-0.1577', '-0.3596', '-0.0724', '0.03146', '0.2793', '-0.0342', '0.555', '0.1274', '-0.0644', '-0.02048', '-0.3271', '0.1195', '-0.5757', '-0.0875', '0.04877', '-0.569', '-0.2413', '-0.5244', '-0.03105', '-0.095', '0.0225', '0.509', '-0.36', '0.1448', '0.2913', '-0.5586', '-0.557', '0.1049', '-0.256', '-0.0885', '0.1052', '0.0629', '-0.1486', '0.5903', '-0.283', '0.0435', '0.1348', '0.1377', '-0.572', '-0.2272', '0.201', '0.5234', '-0.2112', '0.07196', '0.1023', '0.8306', '0.5083', '-0.4539', '0.2627', '0.1731', '0.1326', '-0.7397', '-0.2986', '-0.2244', '0.1377', '0.7305', '-0.2467', '0.3855', '-0.06042', '0.2683', '0.01134', '0.831', '0.4333', '-0.3079', '0.3396', '0.5747', '-0.2319', '-0.2346', '0.4268', '0.1587', '0.4954', '-0.3975', '0.2913', '0.135']",,,,,,,
mondo:0019451,chronic neutrophilic leukemia,"['chronic neutrophilic leukemia', 'CNL', 'neutrophilic leukaemia', 'neutrophilic leukemia']",0080187,,86829,C0474856,,C3179,1000179,D015467,,,,
mondo:0019452,"myeloproliferative neoplasm, unclassifiable","['chronic myeloproliferative disease, unclassifiable', 'MPN-U', 'chronic myeloproliferative disorder, unclassifiable', 'unclassifiable chronic myeloproliferative disorder', 'CMPD, U', 'unclassifiable chronic myeloproliferative disease', 'MPN, U', 'myeloproliferative neoplasm, unclassifiable', 'CMPD-U', 'undifferentiated myeloproliferative disease']",,,86830,C1333046,,C27350,,,,,,
mondo:0019453,myelodysplastic syndrome with multilineage dysplasia,"['MDS-MLD', 'refractory cytopenia with multilineage dysplasia', 'RCMD']",,,86836,C0796466,,C8574,,,238.72,D46.A,10067959,
mondo:0019454,myelodysplastic syndrome with excess blasts,"['myelodysplastic syndrome with Excess blasts', 'refractory Anemia with Excess blasts', 'MDS-EB', 'refractory Anaemia with Excess blasts', 'refractory Anaemia with an Excess of blasts', 'RAEB', 'refractory Anemia with an Excess of blasts']",,,86839,C0002894,,C7506,0003811,D000754,,,10038270,
mondo:0019455,acute panmyelosis with myelofibrosis,"['acute (malignant) myelosclerosis', 'acute myelodysplasia with myelofibrosis', 'acute (malignant) myelofibrosis', 'acute myelofibrosis', 'acute panmyelosis', 'APMF', 'acute myelosclerosis']",,,86843,C0334674,,C4344,,,289.89,,10000879,
mondo:0019456,acute myeloid leukemia with multilineage dysplasia,"['acute myeloid leukemia with myelodysplasia-related features', 'De novo acute myeloid leukemia with multilineage dysplasia', 'AML with myelodysplasia-related features', 'acute myeloid leukaemia with myelodysplasia-related features', 'AML with multilineage dysplasia', 'De novo acute myeloid leukaemia with multilineage dysplasia']",,,86845,C1292773,,C9289,,,,,,
mondo:0019457,therapy related acute myeloid leukemia and myelodysplastic syndrome,"['Secondary Acute myeloblastic Leukaemia', 'secondary acute myeloid leukemia', 'therapy-related AML and myelodysplastic syndrome', 'Secondary Acute myelocytic Leukaemia', 'Secondary Acute granulocytic Leukemia', 'Secondary Acute myelogenous Leukaemia', 'secondary acute myeloid leukaemia', 'Secondary Acute myeloid Leukaemia (AML)', 'Secondary AGL', 'Secondary Acute granulocytic Leukaemia', 'Secondary Acute myelocytic Leukemia', 'Secondary Acute myeloid Leukemia (AML)', 'secondary AML', 'Secondary Acute myelogenous Leukemia', 'Secondary Acute myeloblastic Leukemia']",,,86846,,,C25765,,,,,,
mondo:0019458,acute basophilic leukemia,"['basophilic leukemia', 'leukaemia basophilic', 'basophilic leukaemia', 'leukemia basophilic']",0080795,,86849,C0221292,,C3164,0003029,D015471,,,,
mondo:0019460,acute leukemia of ambiguous lineage,"['hybrid acute leukaemia', 'mixed phenotype acute leukaemia', 'acute leukaemia of indeterminate lineage', 'mixed phenotype acute leukemia', 'ALL with myeloid markers', 'acute leukemia of indeterminate lineage', 'acute leukemia of ambiguous lineage', 'hybrid acute leukemia', 'AML with lymphoid markers', 'mixed lineage acute leukaemia', 'BAL', 'biphenotypic acute leukaemia', 'acute leukemia of undetermined lineage', 'mixed lineage acute leukemia', 'biphenotypic acute leukemia', 'acute leukaemia of undetermined lineage']",,,86851,C1301357,,C7464,,,,,10067399,
mondo:0019461,B-cell prolymphocytic leukemia,"['B prolymphocytic leukaemia', 'B prolymphocytic leukemia', 'BPLL', 'B-PLL', 'B-cell prolymphocytic leukemia']",0081041,,86852,C0475801,,C4753,1000102,D054403,,,,
mondo:0019462,splenic marginal zone lymphoma,"['marginal zone lymphoma of the spleen', 'SMZL', 'splenic marginal zone B-cell lymphoma with villous lymphocytes', 'splenic lymphoma with circulating villous lymphocytes', 'splenic marginal zone lymphoma', 'marginal zone lymphoma of spleen', 'splenic marginal zone B-cell lymphoma', 'SLVL', 'splenic marginal zone lymphoma with villous lymphocytes']",0050750,,86854,C0349632,,C4663,1000550,,,,10062113,
mondo:0019463,non-amyloid monoclonal immunoglobulin deposition disease,"['Randall disease', 'non-amyloid MIDD']",,,86861,CN206242,,,,,,,,
mondo:0019464,heavy chain disease,"['HCD', 'heavy chain disease']",0060125,,86864,C0018852,,C3082,1001341,D006362,273.2,C88.3,10019350,
mondo:0019465,nodal marginal zone B-cell lymphoma,"['nodal marginal zone lymphoma', 'nodal marginal zone B-cell lymph.', 'nodal marginal zone B-cell lymphoma', 'NMZL', 'Monocytoid B-cell lymphoma']",0080211,,86867,C0855139,,C8863,,,,,10029460,
mondo:0019466,lymphomatoid granulomatosis,['LYG'],0081307,,86869,C0024307,,C7930,,D008230,,,10025325,
mondo:0019467,CD4+/CD56+ hematodermic neoplasm,"['CD4+/CD56+ hematodermic neoplasm', 'blastic NK-cell lymphoma', 'blastic plasmacytoid Dendritic cell neoplasm', 'blastic plasmacytoid dendritic cell neoplasm', 'BPDCN', 'lymphoblastoid variant of NK-cell lymphoma', 'primary cutaneous CD4+/CD56+ hematolymphoid neoplasm', 'blastic plasmacytoid dendritic cell', 'agranular CD4+ natural Killer cell leukemia', 'agranular CD4+ natural Killer cell leukaemia', 'monomorphic NK-cell lymphoma', 'agranular CD4+ CD56+ hematodermic neoplasm/tumor', 'blastic natural Killer leukemia/lymphoma', 'early plasmacytoid Dendritic cell leukemia/lymphoma']",0081076,,86870,CN206246,,C7203,,,202.80,,,
mondo:0019468,T-cell prolymphocytic leukemia,"['chronic T-cell leukaemia', 'T cell chronic lymphocytic leukaemia', 'T cell prolymphocytic leukemia', 'leukemia, T-cell, chronic', 'T-cell prolymphocytic leukemia', 'chronic T-cell leukemia', 'T-cell chronic lymphocytic leukaemia', 'CLL, T-cell', 'T prolymphocytic leukemia', 'T cell prolymphocytic leukaemia', 'T cell CLL', 'T prolymphocytic leukaemia', 'T cell chronic lymphocytic leukemia', 'T-cell chronic lymphocytic leukemia', 'T-PLL', 'T-cell CLL', 'chronic T-cell lymphocytic leukemia', 'chronic T-cell lymphocytic leukaemia', 'TPLL']",0081042,,86871,C2363142,,C70649,1000560,D015461,,,10042985,
mondo:0019469,T-cell large granular lymphocyte leukemia,"['T-cell LGL leukemia', 'T-cell large granular lymphocytic leukaemia', 'large cell granular lymphogenous leukemia', 'T-gamma lymphoproliferative disorder', 'T-cell large gran. lymph. leuk.', 'T-LGL', 'LGLL', 'proliferation of large granular lymphocytes', 'large granular lymphocytic leukaemia', 'T-cell large granular lymphocyte leukemia', 'leukemia, large granular LYMPHOCYTIC, malignant', 'large cell granular lymphoid leukemia', 'TLGL', 'large cell granular lymphoid leukaemia', 'large cell granular lymphogenous leukaemia', 'Tgamma large granular lymphocyte leukaemia', 'LGL leukaemia', 'LGL leukemia', 'T-cell large granular lymphocytic leukemia', 'large granular lymphocytic leukemia', 'Tgamma large granular lymphocyte leukemia', 'T-LGL leukemia', 'large granular lymphocyte leukemia', 'large granular lymphocyte leukaemia', 'T-LGL leukaemia', 'T gamma lymphoproliferative disorder', 'large granular lymphocytosis', 'T-cell LGL leukaemia']",0050751,,86872,C1955861,,C4664,,,204.80,,10065862,
mondo:0019470,aggressive NK-cell leukemia,"['NK-cell LGL leukaemia', 'natural killer cell leukaemia', 'natural Killer cell leukaemia', 'NK-cell LGL leukemia', 'aggressive natural killer cell leukemia', 'aggressive NK-cell leukemia (morphologic abnormality)', 'natural Killer cell leukemia', 'NK-cell leukaemia', 'NK-cell leukemia', 'aggressive NK cell leukemia', 'aggressive NK-cell leukaemia (morphologic abnormality)', 'aggressive NK-cell leukemia/lymphoma', 'NK-cell large granular lymphocyte leukaemia', 'natural killer cell leukemia', 'large granular lymphocyte leukemia, NK-cell type', 'aggressive NK cell leukaemia', 'NK cell leukaemia', 'NK-cell large granular lymphocyte leukemia', 'aggressive NK-cell leukemia', 'aggressive natural killer cell leukaemia', 'aggressive NK-cell lymphoma', 'leukaemia (disease) of natural killer cell', 'ANKL', 'NK cell leukemia', 'natural killer cell leukaemia (disease)', 'ANKCL', 'natural killer cell leukemia (disease)']",1035,,86873,C1522378,,C8647,,,,,10028811,
mondo:0019471,adult T-cell leukemia/lymphoma,"['HTLV-I associated adult T-cell leukemia/lymphoma', 'HTLV-1 associated adult T-cell lymphoma/leukemia', 'adult T-cell leukemia/lymphoma (HTLV-1 positive)', 'T-cell leukaemia of adults', 'adult T cell lymphoma/leukemia', 'adult T-cell lymphoma', 'adult T-cell leukaemia', 'adult T-cell leukemia/lymphoma', 'ATLL', 'adult T-cell lymphoma/leukemia', 'adult T-cell leukemia', 'T-cell leukemia of adults']",0050523,,86875,C0023493,,C3184,,,204.80,,10001413,
mondo:0019472,extranodal nasal NK/T cell lymphoma,"['reticulosis, malignant', 'nasal type Extranodal NK/T-cell lymphoma', 'angiocentric T-cell lymphoma', 'Extranodal NK/T lymphoma-nasal', 'Extranodal NK/T-cell lymphoma, nasal type', 'nasal T/natural killer-cell lymphoma', 'NK/T-cell lymphoma', 'lethal midline granuloma', 'NKTCL']",0080797,,86879,C0392788,,C4684,,,,,10065855,
mondo:0019473,enteropathy-associated T-cell lymphoma,"['enteropathy associated T-cell lymphoma', 'high-grade pleomorphic peripheral T-cell lymphoma', 'ETTL', 'enteropathy-type T-cell lymphoma', 'EATCL', 'enteropathy-associated T-cell lymphoma, type I', 'EATL, type I', 'EATL', 'intestinal T-cell lymphoma']",,,86880,C0456889,,C4737,,D058527,202.70,,10022703,
mondo:0019474,hepatosplenic T-cell lymphoma,"['Hepatosplenic gamma/Delta T-cell lymphoma', 'HSTCL']",0081049,,86882,C1333984,,C8459,,,202.80,C86.1,10066957,
mondo:0019475,subcutaneous panniculitis-like T-cell lymphoma,"['T-CELL LYMPHOMA, SUBCUTANEOUS PANNICULITIS-LIKE', 'subcutaneous panniculitic T-cell lymphoma', 'SPTCL', 'subcutaneous panniculitis-like T-cell lymphoma', 'subcutaneous panniculitis-like T-cell lymphoma, Alpha/Beta type', 'subcutaneous panniculitis-like T-cell lymphoma (Alpha/Beta type)']",,618398,86884,C0522624,"['-0.3237', '0.3013', '-0.007694', '-0.498', '-0.4553', '-0.4255', '0.3762', '0.875', '0.2026', '-0.3025', '0.547', '0.3596', '-0.8306', '0.07965', '-0.3215', '0.3176', '-0.8296', '-0.4473', '-0.2747', '-0.3772', '-0.09406', '0.01431', '0.4038', '-0.2023', '0.0204', '0.3005', '-0.2299', '-0.07947', '-0.4556', '-0.5605', '1.14', '0.4302', '0.609', '-0.315', '0.72', '-0.1522', '-1.522', '0.269', '0.168', '-0.04514', '0.1559', '-0.1405', '-0.3848', '-0.3174', '0.184', '0.2339', '-0.4912', '-0.2496', '0.616', '-0.3628', '-0.3237', '-0.11285', '0.4453', '0.259', '-0.7007', '0.4004', '-0.1532', '-0.588', '-0.3743', '-0.1367', '0.04266', '0.1461', '0.0645', '-0.4338', '0.3225', '0.1967', '0.319', '0.569', '0.287', '1.531', '-0.2189', '0.17', '-0.4802', '-0.4883', '0.1871', '-0.011345', '-0.03284', '0.7344', '0.1263', '-0.3967', '-0.2827', '-0.02693', '0.46', '-0.1664', '-0.294', '0.03748', '0.396', '-0.0886', '0.2191', '0.2646', '0.887', '-0.2472', '0.1836', '0.02626', '0.7617', '0.1384', '-0.1254', '0.0431', '-0.346', '-0.11804']",C6918,1000552,C537503,202.70,C86.3,,
mondo:0019476,primary cutaneous peripheral T-cell lymphoma not otherwise specified,['primary cutaneous unspecified peripheral T-cell lymphoma'],,,86885,,,,,D016411,,C84.4,10034623,
mondo:0019478,adult nodular lymphocyte predominant Hodgkin lymphoma,"['nodular lymphocyte predominant Hodgkin lymphoma', 'adult nodular lymphocyte predominant Hodgkin^s disease', 'adult nodular lymphocyte predominant Hodgkin^s lymphoma', 'adult NLPHD']",,,,C1332210,,C7942,,,,,,
mondo:0019479,histiocytic sarcoma,"['histiocytic sarcoma', 'sarcoma, histiocytic, malignant']",0080915,,86896,C0334663,,C27349,,D054747,171.9,C96.A,,
mondo:0019480,Langerhans cell sarcoma,"['sarcoma of Langerhans cell', 'malignant Langerhans cell sarcoma', 'LCS', 'Langerhans cell sarcoma']",7146,,86897,C1260327,,C6921,0007336,D054752,,,,
mondo:0019482,dendritic cell sarcoma not otherwise specified,,,,86903,,,,,,,,,
mondo:0019483,methotrexate-associated lymphoproliferative disorders,"['MTX-associated lymphoproliferative disorders', 'methotrexate-associated lymphoproliferation', 'MTX-LPD', 'methotrexate-associated lymphoproliferative disorder']",5821,,86904,CN206264,,C7184,,,,,,
mondo:0019484,hypothalamic hamartomas with gelastic seizures,,,,86906,,,,,,,,,
mondo:0019485,idiopathic hemiconvulsion-hemiplegia syndrome,"['HHE syndrome', 'hemiconvulsion-hemiplegia-epilepsy syndrome', 'IHHS']",,,86908,,,,,,,,,
mondo:0019486,myoclonic epilepsy of infancy,"['benign myoclonus epilepsy of infancy', 'benign myoclonic epilepsy of infancy']",,,86909,CN206266,,,,,,,,
mondo:0019487,epilepsy with myoclonic absences,,,,86911,,,,,,,,,
mondo:0019488,myoclonic epilepsy in non-progressive encephalopathies,"['myoclonus epilepsy in non-progressive encephalopathies', 'myoclonic status in non-progressive encephalopathies']",,,86913,,,,,,,,,
mondo:0019489,diffuse palmoplantar keratoderma - acrocyanosis syndrome,['diffuse palmoplantar hyperkeratosis-acrocyanosis syndrome'],,,86918,CN206272,,,,,,,,
mondo:0019490,progressive familial heart block,"['familial progressive heart block', 'familial Lenegre disease', 'hereditary bundle branch defect', 'familial Lev-Lenègre disease', 'PFHB', 'familial progressive cardiac conduction defect', 'familial Lenègre disease', 'familial Lev-Lenegre disease', 'familial PCCD', 'familial Lev disease']",0111073,,871,CN206278,,,,,426.6,,,
mondo:0019493,primary adult heart tumor,"['adult heart tumour', 'adult cardiac tumor', 'adult cardiac tumour', 'adult heart tumor']",,,874,CN206280,,,,,,D15.1,,
mondo:0019494,primary pediatric heart tumor,"['pediatric heart neoplasm', 'Cardiac tumor of child', 'heart tumour of child', 'heart tumor of child', 'Cardiac tumour of child', 'paediatric heart neoplasm']",,,875,CN206281,,,,,,D15.1,,
mondo:0019496,neuroendocrine neoplasm,"['neuroendocrine tumor', 'neuroendocrine neoplasm', 'neuroendocrine tumour', 'APUDoma']",169,,877,CN206284,,C3809,1001901,D018358,239.7,,,
mondo:0019497,nonsyndromic genetic hearing loss,"['nonsyndromic deafness', 'familial deafness', 'nonsyndromic genetic deafness', 'nonsyndromic hereditary hearing loss', 'nonsyndromic hearing loss', 'isolated genetic deafness', 'non-syndromic genetic deafness']",0050563,,87884,CN043648,"['0.2192', '0.7974', '-0.1346', '0.0867', '0.5234', '0.06012', '0.526', '0.3987', '-0.4666', '-0.6807', '-0.1686', '-0.576', '-0.424', '0.5703', '0.001895', '-0.551', '0.0343', '-0.304', '-0.10095', '-0.2198', '0.02888', '-0.442', '-0.1418', '0.2532', '0.2725', '0.3838', '-0.7095', '0.01701', '0.2231', '-0.001999', '-0.1915', '0.4355', '-0.04453', '0.508', '-0.281', '-0.1144', '-0.2966', '-0.4177', '-0.2651', '0.002218', '0.1385', '-0.2365', '0.516', '-0.4756', '0.08276', '-0.1982', '-0.621', '-0.5684', '-0.03867', '0.2507', '0.3923', '-0.906', '-0.2252', '-0.00426', '-0.3428', '-0.0783', '0.1549', '-0.083', '-0.2678', '0.543', '-0.0747', '-0.1655', '0.007343', '-0.01974', '-0.6816', '0.5034', '-0.3896', '0.6123', '0.014366', '0.4836', '-0.02481', '-0.2009', '0.437', '-0.622', '0.4683', '-0.11505', '0.7817', '0.3484', '-0.701', '-0.11304', '-0.1101', '-0.529', '0.0601', '0.6123', '-0.1385', '-0.414', '0.5107', '0.627', '-0.5005', '0.7744', '0.423', '0.4312', '0.1902', '0.0918', '0.956', '-0.489', '0.703', '-0.895', '0.07007', '0.336']",,0009076,C580334,,,,
mondo:0019498,tungiasis,"['Tunga penetrans caused disease or disorder', 'T penetrans', 'Sarcopsylla penetrans', 'chigger flea', 'S penetrans', 'Tunga penetrans']",0050266,,879,C0277356,,,1001445,D058285,134.1,,,
mondo:0019499,Turner syndrome,"['45,X/46,XX syndrome', '45,X gonadal dysgenesis', 'gonadal dysgenesis Turner type', 'karyotype 45, X', 'gonadal dysgenesis (45,X)', 'Turner Varny syndrome', '45, X syndrome', 'Schereshevkii Turner syndrome', 'Bonnevie-Ullrich syndrome', 'Ullrich-Turner syndrome', 'chromosome X monosomy X', 'monosomy X', 'XO syndrome', '45X syndrome', 'gonadal dysgenesis', 'gonadal dysgenesis - Turner', 'monosomy X syndrome', '45,X syndrome', 'genital dwarfism', 'genital dwarfism, Turner type', '45,X0 syndrome']",3491,,881,C0041408,,C26900,,D014424,758.7,,10045181,
mondo:0019500,extragonadal teratoma,,,,883,,,,,D013724,,,10043276,
mondo:0019501,Usher syndrome,"['retinitis pigmentosa-deafness syndrome', 'Hallgren syndrome', 'Usher^s syndrome', 'Graefe-Usher syndrome', 'dystrophia retinae pigmentosa-dysostosis syndrome', 'ush', 'deafness-retinitis pigmentosa syndrome']",0050439,,886,C0271097,"['0.0782', '-0.2876', '-0.02867', '0.0769', '0.1654', '-0.4539', '0.511', '0.789', '-1.119', '-0.672', '-0.1455', '-0.06885', '0.09143', '0.0908', '0.02428', '-0.643', '-0.2341', '0.0328', '0.10785', '-0.0831', '-0.0204', '-0.267', '0.0979', '0.0012455', '-0.504', '0.2133', '-0.776', '-0.2206', '-0.5684', '0.1735', '0.5806', '0.0929', '0.0781', '0.291', '-0.3547', '-0.1753', '-0.0509', '-0.09436', '-0.4817', '0.04147', '-0.2416', '0.301', '0.1886', '-0.1339', '0.1477', '0.06683', '-0.4011', '-0.431', '-0.2146', '0.4624', '0.3386', '-0.4504', '-0.0907', '-0.733', '0.2954', '0.2683', '0.9165', '-0.255', '-0.747', '0.4148', '-0.10944', '-0.1458', '0.6055', '0.2742', '-0.1624', '-0.2966', '-0.1798', '0.4133', '0.05518', '0.4514', '-0.5522', '0.05835', '-0.1505', '-0.3232', '1.368', '-0.2988', '0.168', '-0.179', '-0.3787', '0.02545', '0.06665', '-0.637', '-0.503', '1.639', '-0.762', '0.06726', '0.272', '0.5347', '-0.009346', '0.495', '0.2245', '0.4976', '0.2443', '0.4011', '0.6904', '-0.3684', '0.3118', '-1.152', '0.2238', '0.01064']",C85217,,D052245,,H35.5,10063396,
mondo:0019502,autosomal recessive non-syndromic intellectual disability,"['AR-NSID', 'mental retardation, autosomal recessive', 'non-syndromic intellectual disability, autosomal recessive', 'autosomal recessive intellectual disability', 'autosomal recessive non-syndromic mental retardation', 'NS-ARID', 'autosomal recessive non-syndromic intellectual disability', 'autosomal recessive mental retardation', 'intellectual disability, autosomal recessive']",0060308,,88616,CN206293,"['-0.08575', '0.1033', '0.1388', '-0.1586', '0.1523', '-0.2479', '-0.02054', '0.2249', '-0.1209', '-0.2257', '-0.0989', '-0.03366', '0.01611', '-0.04205', '0.098', '-0.02116', '0.03093', '-0.04535', '-0.086', '-0.4243', '-0.08777', '0.0971', '0.0808', '-0.03754', '0.1321', '0.02185', '-0.04666', '-0.0726', '0.05966', '-0.1617', '0.0901', '0.0634', '0.281', '0.1665', '-0.05533', '-0.102', '-0.06287', '-0.251', '-0.013756', '-0.2351', '0.135', '-0.2798', '0.0367', '0.003784', '-0.1007', '-0.3054', '-0.03168', '0.06805', '0.02594', '-0.00631', '-0.02411', '-0.001159', '-0.014725', '-0.1674', '-0.007587', '-0.1127', '0.1392', '0.02766', '-0.1951', '0.1267', '0.11096', '-0.00353', '0.11', '0.02257', '0.02446', '0.007603', '0.06824', '0.1746', '-0.1804', '0.1578', '-0.254', '-0.04654', '0.06274', '-0.1566', '0.10803', '0.1378', '0.0942', '-0.04144', '-0.1865', '-0.01576', '-0.03912', '0.010735', '-0.07996', '0.2817', '0.12195', '0.06525', '0.05136', '0.1887', '0.1528', '0.2407', '0.11725', '0.3584', '-0.002522', '0.02756', '0.4487', '0.1071', '0.2761', '-0.299', '0.1742', '0.1715']",,,,,,,
mondo:0019503,anterior segment dysgenesis,"['anterior segment mesenchymal dysgenesis', 'familial ocular anterior segment mesenchymal dysgenesis', 'ASGD', 'ASOD', 'anterior segment ocular dysgenesis', 'ASMD']",0060648,,88632,,"['-0.3484', '0.12384', '0.3257', '-0.2031', '0.2861', '0.0249', '0.1278', '0.2234', '-0.3672', '-0.005234', '-0.3643', '-0.2299', '0.04916', '0.2144', '-0.4194', '-0.2546', '0.0242', '-0.03925', '-0.0323', '-0.466', '0.03207', '-0.0833', '0.1682', '-0.2588', '0.0628', '0.02678', '-0.2201', '0.2986', '0.0912', '0.00805', '0.11975', '0.1488', '0.2418', '0.02809', '0.0891', '0.0649', '0.1278', '-0.000517', '-0.12396', '-0.478', '0.3716', '-0.003147', '-0.009964', '-0.1459', '-0.09424', '-0.2546', '0.2198', '0.07654', '0.2856', '0.0798', '0.064', '-0.01978', '0.01851', '-0.1493', '-0.1641', '-0.1527', '0.2186', '0.06525', '-0.4006', '0.02434', '0.1515', '-0.1007', '-0.09546', '0.4827', '-0.1938', '0.02513', '0.4348', '0.2969', '-0.2449', '0.1156', '-0.2123', '0.333', '0.125', '0.2954', '-0.06885', '0.02695', '0.02324', '0.1611', '-0.3132', '-0.3699', '0.0992', '0.2024', '-0.066', '0.3564', '-0.2966', '-0.4058', '0.1766', '0.2081', '0.1077', '0.03458', '0.148', '0.4714', '0.159', '0.014786', '0.4924', '-0.4414', '0.2844', '-0.1837', '-0.0743', '0.188']",,,,743.49,,,
mondo:0019504,superior limbic keratoconjunctivitis,"['Theodore^s syndrome', 'Theodores syndrome', 'SLK', 'Theodore^s superior limbic keratoconjunctivitis', 'Theodores superior limbic keratoconjunctivitis']",,,88633,C0339229,,,,,370.49,H16.2,,
mondo:0019505,hypomyelination-hypogonadotropic hypogonadism-hypodontia syndrome,['4H syndrome'],,,88637,CN206304,,,,,,,,
mondo:0019506,obesity-colitis-hypothyroidism-cardiac hypertrophy-developmental delay syndrome,,,,88643,CN227640,,,,,,,,
mondo:0019507,amelogenesis imperfecta,,2187,,88661,,"['0.2164', '0.01955', '0.035', '-0.04132', '0.71', '0.3', '0.4207', '0.402', '-0.05048', '-0.3352', '-0.4768', '-0.569', '-0.3025', '0.1587', '0.3083', '-0.2654', '-0.5015', '-0.438', '-0.2485', '-1.059', '-0.3308', '-0.172', '0.713', '-0.627', '0.2976', '0.0836', '-0.286', '0.405', '0.013725', '-0.1812', '0.07336', '0.2202', '-0.02895', '0.3896', '0.5654', '0.3574', '-0.1182', '-0.529', '-0.04544', '-0.6265', '-0.05273', '0.4233', '-0.4414', '-0.566', '-0.165', '-0.1364', '-0.1754', '-0.3694', '0.4814', '-0.06107', '0.392', '-0.313', '0.1721', '-0.0445', '0.319', '0.02562', '0.4822', '-0.1687', '0.1311', '-0.3232', '0.1738', '0.10016', '0.1959', '-0.1447', '0.1102', '0.367', '0.2454', '0.4824', '0.10034', '-0.1521', '-0.719', '0.1772', '0.443', '-0.0662', '0.536', '0.0461', '0.201', '-0.2333', '-0.1078', '-0.8613', '0.08435', '0.0792', '0.2578', '0.564', '0.2368', '0.02495', '-0.2534', '-0.07153', '0.3699', '0.2803', '-0.0919', '-0.1559', '-0.366', '0.7515', '0.0722', '0.0227', '0.07526', '-0.6006', '0.3132', '0.4514']",,,D000567,520.5,,,
mondo:0019508,van der Woude syndrome,"['lip-pit syndrome', 'VWS', 'cleft lip and/or palate with mucous cysts of lower lip', 'lip pit syndrome', 'LPS', 'cleft lip/palate with mucous cysts of lower lip']",0060239,604547,888,C0175697,"['1.181', '0.05383', '0.013054', '-0.7266', '0.37', '0.2297', '0.2812', '0.8896', '-0.5146', '-0.7036', '0.04053', '-0.2546', '-0.1295', '0.6865', '0.1572', '0.01587', '-0.2683', '-0.6406', '-0.3726', '-0.4436', '-0.2406', '0.09845', '0.7646', '0.3787', '0.2595', '0.1417', '-0.5894', '-0.0937', '0.7236', '-0.538', '0.4036', '-0.2534', '-0.1471', '0.09', '-0.194', '-0.04935', '-0.326', '-0.00992', '-0.29', '0.1255', '0.0392', '0.5825', '0.839', '-0.3228', '0.0649', '-0.5146', '-0.2546', '-0.1273', '-0.0806', '0.0996', '-0.9473', '-0.569', '-0.3525', '-0.4014', '-0.623', '0.06433', '0.414', '-0.666', '-0.1306', '0.2229', '0.195', '0.2856', '0.1304', '-0.01767', '-0.244', '-0.01221', '0.00942', '-0.04648', '-0.2146', '0.342', '-0.4038', '-0.0574', '-0.04556', '-0.2627', '0.425', '0.01106', '0.614', '-0.3235', '-0.6455', '0.03278', '0.0658', '-0.3342', '0.0635', '0.3557', '-0.4993', '0.5186', '-0.1869', '0.5444', '-0.09186', '0.506', '-0.562', '0.2498', '-0.2128', '0.3015', '1.014', '-0.4597', '0.1456', '-0.6143', '0.426', '0.5137']",C74986,,C536528,744.89,,,
mondo:0019509,cutaneous leukocytoclastic angiitis,"['cutaneous leukocytoclastic vasculitis', 'hypersensitivity angiitis', 'cutaneous small vessel vasculitis', 'cutaneous hypersensitivity vasculitis', 'cutaneous small-vessel vasculitis', 'leukocytoclastic angiitis']",,,889,,,C122919,,,,,,
mondo:0019512,congenital heart malformation,"['disorder of heart development', 'congenital heart malformation', 'rare congenital non-syndromic heart malformation', 'congenital non-syndromic heart malformation', 'heart development disease']",,,88991,,"['-0.224', '0.01677', '0.1313', '0.0273', '0.2292', '-0.2064', '0.03918', '0.257', '-0.2349', '-0.1276', '-0.11304', '-0.1571', '-0.03029', '-0.003649', '-0.08936', '-0.1322', '-0.2384', '-0.1076', '-0.1769', '-0.357', '0.11426', '0.06354', '0.1478', '-0.163', '0.1814', '-0.07526', '-0.03653', '0.02654', '0.0929', '0.0832', '0.2913', '0.1191', '0.2637', '0.10944', '0.0689', '-0.1349', '0.07715', '0.01465', '0.0592', '-0.1938', '0.1875', '-0.05594', '0.12286', '-0.08185', '-0.02165', '-0.2139', '0.06995', '0.138', '-0.0983', '-0.06915', '-0.0962', '0.03265', '0.1024', '0.02841', '-0.1135', '-0.1682', '0.1043', '0.0888', '-0.234', '-0.02884', '0.008064', '0.0886', '0.08826', '0.04944', '-0.01955', '0.07806', '0.1906', '0.158', '-0.3135', '0.1311', '-0.1913', '0.083', '0.0575', '-0.1093', '0.10406', '-0.0145', '-0.03696', '0.10406', '-0.1139', '-0.1277', '0.01959', '0.02943', '-0.006756', '0.1873', '-0.06137', '-0.2256', '0.2546', '0.1445', '0.01666', '0.09235', '0.05853', '0.184', '0.06366', '0.1022', '0.3218', '0.0633', '0.235', '-0.3518', '0.01036', '0.03992']",,0005269,,,,,
mondo:0019513,esophageal malformation,,,,88993,,,,,,,,,
mondo:0019514,hepatic veno-occlusive disease,"['veno-occlusive disease', 'sinusoidal obstruction syndrome', 'liver veno-occlusive disease', 'hepatic Vod']",0080177,,890,C0019156,,C26793,,D006504,453.89,K76.5,10047216,
mondo:0019516,exudative vitreoretinopathy,"['Criswick-Schepens syndrome', 'familial exudative vitreoretinopathy', 'FEVR', 'exudative vitreoretinopathy, familial']",0050535,,891,C4072980,"['-0.1038', '-0.278', '-0.3276', '0.1674', '-0.04898', '-0.0908', '-0.06287', '0.3809', '-0.5146', '0.03925', '-0.2961', '-0.2854', '-0.0906', '0.18', '-0.1472', '0.1637', '-0.001841', '-0.04642', '0.06506', '-0.5293', '-0.3188', '0.1807', '0.3296', '0.124', '-0.4062', '0.1904', '-0.543', '0.3699', '0.578', '0.687', '0.948', '-0.4624', '0.3447', '0.59', '-0.2617', '0.0895', '0.01052', '-0.7617', '-0.3716', '-0.4849', '0.7314', '-0.2048', '0.3442', '-0.4717', '0.0503', '0.01057', '-0.01016', '-0.4607', '0.474', '-0.1708', '0.7563', '0.1326', '0.09033', '-0.2273', '0.5566', '-0.04294', '1.046', '0.1827', '-0.5347', '0.579', '0.1844', '0.2438', '0.165', '0.2617', '-0.334', '0.4954', '0.2073', '0.81', '0.03049', '0.6055', '-0.11725', '-0.1114', '-0.341', '-0.02019', '0.5396', '-0.267', '0.3662', '-0.1208', '-0.0561', '-0.1515', '-0.128', '0.1087', '-0.09894', '0.711', '-0.6826', '-0.401', '0.3953', '0.04974', '0.1555', '-0.04526', '-0.2462', '0.5205', '-0.185', '0.0983', '0.5415', '-0.0594', '0.2722', '-0.1476', '-0.00753', '0.1481']",,,C580083,362.10,,,
mondo:0019517,Waardenburg syndrome type 2,"['WS 2', 'WS2', 'Waardenburg syndrome type II', 'WS type 2']",,,895,C2700265,"['0.741', '-0.0544', '0.03726', '-0.4006', '0.2622', '-0.1891', '-0.02887', '0.2827', '-0.515', '-0.1696', '0.0814', '-0.5947', '-0.4556', '0.4211', '0.0886', '-0.2844', '0.10706', '-0.3774', '-0.138', '-0.4614', '-0.1682', '-0.506', '0.331', '0.1648', '0.01776', '0.3489', '-0.69', '0.2603', '0.3076', '-0.4106', '0.447', '0.09125', '-0.03555', '-0.00856', '0.01127', '-0.0733', '0.04153', '-0.4277', '-0.06995', '0.04898', '0.882', '-0.449', '0.3013', '0.05847', '0.1552', '-0.664', '0.2754', '-0.1869', '0.1488', '0.4736', '-0.11847', '-0.6514', '-0.1469', '-0.5527', '-0.4634', '-0.11847', '0.42', '0.04898', '-0.533', '-0.576', '-0.3655', '-0.422', '0.1159', '-0.07404', '-0.3433', '0.1986', '-0.1681', '-0.02887', '-0.2278', '0.5127', '-0.605', '-0.3574', '-0.0957', '-0.5117', '0.79', '-0.2148', '0.03595', '-0.735', '-0.2418', '-0.1409', '0.8203', '-0.8955', '-0.281', '0.3494', '-0.4807', '-0.3928', '0.4077', '0.4805', '0.0471', '0.2566', '0.09924', '0.74', '0.487', '0.1581', '0.717', '-0.3145', '-0.1753', '-0.567', '-0.06238', '0.0899']",C75009,,C536463,,E70.3,,
mondo:0019518,Waardenburg-Shah syndrome,"['Waardenburg syndrome type 4', 'WS4', 'Waardenburg-Hirschsprung disease', 'Waardenburg syndrome type IV', 'Hirschsprung disease with pigmentary anomaly', 'Waardenburg-Shah syndrome', 'Waardenburg-Hirschsprung syndrome', 'Shah-Waardenburg syndrome']",,,897,CN206330,"['0.1392', '-0.0513', '0.3618', '0.067', '0.8486', '-0.3088', '-0.2161', '0.126', '0.09216', '-0.4084', '-0.05112', '-0.5513', '-0.4255', '0.004787', '-0.0501', '-0.08417', '0.3032', '-0.178', '-0.4243', '-0.3167', '-0.1483', '-0.3608', '-0.4062', '-0.4353', '0.2747', '0.346', '-0.4', '0.3936', '0.647', '-0.007645', '0.0634', '-0.457', '-0.2598', '-0.0868', '-0.00979', '0.0565', '0.04184', '-0.702', '-0.2216', '0.003704', '0.2532', '-0.4888', '0.844', '-0.501', '-0.01602', '-0.877', '0.0116', '-0.2605', '-0.2927', '0.2734', '-0.0575', '-0.3064', '-0.1932', '-0.574', '-0.00934', '0.3245', '0.2281', '0.1464', '-0.6636', '-0.1605', '0.04483', '0.239', '-0.03528', '0.09534', '-0.08936', '0.1062', '0.3113', '0.54', '0.06415', '0.03014', '-0.3135', '-0.1404', '-0.03363', '0.3696', '0.171', '-0.3508', '0.515', '-0.306', '0.07666', '-0.3562', '0.511', '-0.633', '-0.165', '0.7095', '-0.002548', '-0.05682', '0.4297', '0.798', '0.231', '0.1018', '0.426', '0.5513', '0.6465', '0.02618', '0.664', '-0.002003', '0.116', '-0.673', '0.5034', '0.3882']",C124842,,,,,,
mondo:0019520,syndromic lymphedema,"['syndromic lymphedema', 'syndrome associated with lymphedema']",,,89832,CN227645,,,,,,,,
mondo:0019521,centripetalis recessive dystrophic epidermolysis bullosa,"['RDEB, centripetalis', 'centripetal dystrophic epidermolysis bullosa', 'RDEB-Ce', 'centripetal recessive dystrophic epidermolysis bullosa']",,,89841,C4511056,,,,,,,,
mondo:0019522,recessive dystrophic epidermolysis bullosa-generalized other,"['recessive dystrophic epidermolysis bullosa, non-Hallopeau-Siemens type', 'generalised mitis RDEB', 'recessive dystrophic epidermolysis bullosa, generalized intermediate', 'autosomal recessive dystrophic epidermolysis bullosa, generalized other', 'RDEB, generalised intermediate', 'autosomal recessive dystrophic epidermolysis bullosa generalisata mitis', 'recessive dystrophic epidermolysis bullosa, generalised intermediate', 'RDEB-generalized other', 'RDEB generalisata mitis', 'RDEB, generalized intermediate', 'generalized mitis RDEB', 'autosomal recessive dystrophic epidermolysis bullosa, generalised other', 'RDEB-O', 'RDEB, non-Hallopeau-Siemens type']",,,89842,CN206337,,,,,,,,
mondo:0019524,Bartter syndrome type 4,"['Bartter syndrome with sensorineural deafness', 'Bartter syndrome type 4', 'Bartter syndrome type IV']",,,89938,CN206343,"['0.1648', '0.0732', '-0.1715', '-0.3806', '-0.1713', '-0.531', '-0.0774', '0.9463', '-0.2233', '-0.00969', '-0.4358', '-0.2937', '0.07404', '0.0915', '-0.588', '-0.509', '0.1259', '0.4092', '0.555', '-0.585', '-0.2065', '-0.1458', '0.4038', '0.1324', '0.655', '0.6455', '0.02316', '-0.02592', '0.2773', '-0.0877', '0.0875', '0.05765', '0.889', '0.7593', '-0.4585', '0.1422', '0.1924', '0.4856', '-0.2644', '-0.541', '-0.596', '-0.0795', '0.7095', '-0.393', '0.3765', '0.2284', '-0.4138', '0.4507', '0.05957', '0.3108', '0.2471', '-0.2751', '0.3262', '-0.8022', '-0.008934', '-0.007366', '0.01075', '-0.6064', '0.10876', '0.3518', '-0.03062', '0.01509', '0.2408', '-0.106', '-0.2778', '-0.425', '0.191', '0.4307', '-0.3977', '0.569', '0.0274', '0.3484', '0.3972', '-0.1921', '0.1376', '0.0697', '0.3296', '-0.1262', '-0.003311', '0.1501', '0.0414', '0.6216', '-0.695', '-0.1406', '0.10724', '0.2776', '0.1688', '0.0642', '0.5757', '-0.246', '0.534', '0.2869', '-0.0379', '0.002829', '0.3894', '0.4287', '0.2365', '-0.652', '-0.0904', '-0.06085']",,,,,,,
mondo:0019525,tetrasomy X,"['tetra X', '48 XXXX', '48,XXXX syndrome', 'tetrasomy type X', '48 XXXX syndrome', 'quadruple X']",,,9,C0265496,,,,C536502,758.81,,,
mondo:0019526,erythema elevatum diutinum,,0060567,,90000,C0263398,,,,C535509,695.89,L95.1,10056968,
mondo:0019527,undifferentiated connective tissue syndrome,"['undifferentiated connective tissue disease', 'UCTD']",,,90002,C0409999,,C116776,,,,,10071575,
mondo:0019528,inflammatory pseudotumor of the liver,['IgG4-related hepatopathy'],,,90003,,,,,,,,,
mondo:0019529,radiation myelitis,"['delayed radiation myelopathy', 'radiation myelopathy']",,,90021,,,,,,336.8,,,
mondo:0019530,non-syndromic syndactyly,"['nonsyndromic syndactyly', 'chromosome 2q35 duplication syndrome', 'symphalangy', 'webbing of digits', 'symphalangism', 'syndactyly', 'isolated syndactyly']",,,90025,,,C87125,,,,,10042778,
mondo:0019531,hemolytic anemia due to glutathione reductase deficiency,['HEMOLYTIC ANEMIA DUE TO GLUTATHIONE REDUCTASE DEFICIENCY'],,618660,90030,,"['-0.3953', '0.503', '-0.156', '0.1774', '0.684', '0.065', '-0.1565', '0.652', '-0.2104', '-0.631', '0.7256', '-0.1425', '0.389', '0.3298', '-1.041', '0.02379', '-0.54', '0.1946', '-0.6978', '-0.491', '-0.1936', '-0.4597', '0.2805', '-0.11005', '0.67', '-0.5806', '-0.0618', '-0.2554', '0.548', '0.195', '0.010254', '0.03308', '0.5693', '0.605', '0.4497', '-0.4126', '-0.696', '-0.5596', '0.28', '-0.5137', '-0.7676', '0.1427', '-0.2219', '-0.515', '-0.6245', '-0.7163', '0.166', '0.302', '0.2247', '-0.1586', '0.4478', '0.4067', '0.879', '-0.1052', '0.3684', '-0.687', '0.2365', '0.381', '-0.963', '0.1162', '-0.2015', '0.2031', '-0.00825', '-0.248', '-0.073', '0.3528', '0.2457', '0.6333', '-0.585', '0.623', '0.8486', '-0.2793', '-0.6606', '-0.625', '0.4238', '0.941', '0.2208', '0.279', '0.04587', '0.3699', '0.1382', '-0.03238', '0.1339', '-0.1179', '0.618', '-0.42', '-0.4868', '0.391', '0.8203', '-0.02254', '0.6133', '0.385', '-0.339', '0.01317', '0.531', '1.201', '-0.01802', '-0.1292', '0.207', '-0.6504']",,,,,,,
mondo:0019532,"autoimmune hemolytic anemia, warm type","['warm antibody autoimmune hemolytic anaemia', 'warm antibody hemolytic anaemia', 'wAHA', 'warm antibody hemolytic anemia', 'wAIHA', 'warm antibody AIHA', 'warm-reacting-antibody hemolytic anemia', 'warm AIHA', 'warm antibody autoimmune hemolytic anemia', 'warm-reacting-antibody hemolytic anaemia']",,,90033,C0272118,,C162611,,,,,10047822,
mondo:0019533,paroxysmal cold hemoglobinuria,"['Donath-Landsteiner hemolytic anaemia', 'Donath-Landsteiner syndrome', 'hemoglobinuria paroxysmal cold', 'Donath-Landsteiner hemolytic anemia', 'PCH']",,,90035,,,,,,,,,
mondo:0019534,mixed-type autoimmune hemolytic anemia,['mixed AIHA'],,,90036,C4305257,,,,,,,,
mondo:0019535,drug-induced autoimmune hemolytic anemia,['drug-induced AIHA'],,,90037,,,,,,,D59.0,,
mondo:0019536,Shiga toxin-associated hemolytic uremic syndrome,"['typical HUS', 'Shiga-like toxin-associated HUS', 'typical hemolytic-uremic syndrome', 'hemolytic-uremic syndrome with diarrhoea', 'Sxt-HUS', 'hemolytic-uremic syndrome with diarrhea', 'D-plus hemolytic uremic syndrome (D+HUS)', 'D+HUS']",,,90038,CN206363,,,,,,,,
mondo:0019537,hemoglobin D disease,"['hemoglobin D disease', 'Hb-D disease']",5378,,90039,C0272080,,C35344,,,282.7,,10055019,
mondo:0019538,Gaisbock syndrome,"['stress erythrocytosis', 'stress polycythemia', 'Gaisbock^s syndrome', 'Pseudopolycythemia', 'polycythemia, emotional', 'Pseudopolycythaemia', 'Gaisboeck^s syndrome', 'GaisböCK syndrome']",2838,,90041,CN206365,,C27174,,,,,10053885,
mondo:0019540,diffuse alveolar hemorrhage,"['diffuse alveolar hemorrhage (disease)', 'diffuse alveolar haemorrhage (disease)', 'diffuse alveolar hemorrhage']",,,90060,CN206369,,,,,,,,0025420
mondo:0019541,non-infectious posterior uveitis,['non-infectious choroiditis'],,,90061,,,,,,,,,
mondo:0019542,acute liver failure,"['fulminant hepatic failure', 'acute hepatic failure']",,,90062,C0162557,,C84396,,D017114,,,10000804,
mondo:0019543,acquired aneurysmal subarachnoid hemorrhage,,,,90065,CN206370,,,,,,,,
mondo:0019544,cocaine intoxication,,,,90068,,,,,,292.89,,,
mondo:0019545,systemic monochloroacetate poisoning,,,,90069,,,,,,,,,
mondo:0019547,Wells syndrome,"['eosinophilic cellulitis', 'bullous cellulitis with eosinophilia', 'Wells^ syndrome']",,,901,C0343101,,,,C536693,682.9,,,
mondo:0019548,autosomal dominant intermediate Charcot-Marie-Tooth disease,"['CMTDI', 'intermediate Charcot-Marie-Tooth disease, autosomal dominant', 'autosomal dominant intermediate Charcot-Marie-Tooth']",,,90114,CN206376,,,,,,,,
mondo:0019549,severe early-onset axonal neuropathy due to MFN2 deficiency,"['SEOAN due to MFN2 deficiency', 'autosomal recessive Charcot-Marie-Tooth disease, Ouvrier type', 'AR-CMT2, Ouvrier type']",,,90118,CN206378,,,,,,,,
mondo:0019550,hereditary motor and sensory neuropathy with acrodystrophy,"['autosomal recessive Charcot-Marie-Tooth type 2 with acrodystrophy', 'HMSN with acrodystrophy', 'autosomal recessive axonal Charcot-Marie-Tooth disease with acrodystrophy', 'AR-CMT2 with acrodystrophy']",,,90119,CN206379,,,,,,,,
mondo:0019551,hereditary motor and sensory neuropathy type 6,"['peripheral neuropathy and optic atrophy', 'CMT6', 'hereditary motor and sensory neuropathy type 6', 'Charcot-Marie-Tooth disease type 6']",0080068,,90120,C0393807,"['-0.2673', '0.0729', '0.492', '-0.02184', '-0.2551', '-0.3176', '0.10315', '0.4246', '-0.68', '0.2323', '-0.3232', '-0.05225', '-0.358', '0.1724', '0.03458', '-0.1693', '0.03888', '-0.1326', '-0.1205', '-0.517', '0.2217', '-0.1348', '0.02489', '0.53', '-0.1829', '-0.0348', '0.01678', '0.02634', '-0.453', '0.02562', '0.319', '0.0631', '0.2095', '0.1898', '0.2484', '-0.4514', '-0.3809', '-0.3142', '-0.2786', '-0.1038', '-0.2603', '-0.3494', '0.03842', '0.415', '-0.1145', '-0.2083', '-0.09503', '0.03592', '-0.01765', '0.378', '-0.02559', '0.307', '-0.0823', '-0.303', '0.03122', '-0.1923', '0.03473', '-0.078', '-0.1866', '0.01331', '-0.1632', '-0.3904', '0.1962', '0.4648', '-0.541', '0.2808', '0.1727', '0.9717', '-0.10333', '0.568', '-0.346', '0.1285', '0.2722', '-0.3855', '0.5703', '-0.0087', '0.2194', '0.389', '0.0917', '-0.3572', '-0.11237', '-0.5415', '0.2637', '1.052', '-0.248', '0.1324', '-0.1105', '0.2788', '0.1666', '-0.3337', '0.3638', '0.2004', '0.1437', '0.1787', '0.4863', '0.1613', '0.4663', '-0.1552', '0.0678', '0.4207']",,,,,,,
mondo:0019552,centrifugal lipodystrophy,['lipodystrophia centrifugalis abdominalis infantilis'],,,90156,,,,,,,,,
mondo:0019553,drug-induced localized lipodystrophy,['lipoatrophy caused by injected drug'],,,90157,CN227649,,,,,,,,
mondo:0019554,idiopathic localized lipodystrophy,,,,90158,CN227650,,,,,,,,
mondo:0019555,panniculitis and localized lipodystrophy,"['panniculitis-induced localized lipodystrophy', 'panniculitis-induced localised lipodystrophy']",,,90159,CN227651,,,,,,,,
mondo:0019556,pressure-induced localized lipoatrophy,"['lipoatrophia semicircularis', 'semicircular lipoatrophy']",,,90160,CN227652,,,,,,,,
mondo:0019557,chilblain lupus,"['CHLE', 'Hutchinson lupus']",0060386,,90280,CN239336,"['0.3242', '-0.387', '-0.2266', '-0.0794', '0.1355', '-0.5874', '-0.2072', '-0.3174', '-0.4966', '0.4966', '0.0993', '-0.0229', '-0.0854', '-0.1392', '-0.2551', '-0.5186', '0.286', '0.2351', '-0.2878', '-0.621', '-0.3225', '0.003098', '0.384', '-0.698', '0.02258', '-0.4214', '-0.2898', '0.1251', '-0.4966', '-0.01567', '0.9834', '-0.494', '0.7188', '-0.483', '0.3572', '0.006702', '-0.225', '-0.1688', '0.2656', '-0.358', '0.0826', '-0.1499', '0.325', '-0.5586', '0.2102', '0.249', '-0.2106', '-0.11584', '0.12067', '-0.03726', '-0.2169', '0.10156', '0.509', '-0.09344', '-0.3406', '0.5024', '-0.1604', '0.2025', '-0.2852', '-0.694', '0.1703', '0.518', '-0.432', '-0.02423', '-0.855', '0.18', '0.4011', '1.235', '-0.1848', '0.974', '0.3188', '-0.01324', '0.1224', '-0.1231', '0.05145', '0.1794', '0.5747', '0.644', '0.6685', '-0.587', '-0.1159', '-0.422', '-0.0689', '-0.3599', '0.4302', '-0.4495', '-0.3242', '0.3948', '0.454', '0.3325', '0.4382', '-0.06134', '0.149', '0.976', '0.1443', '0.8623', '-0.2048', '-0.03464', '-0.1367', '-0.343']",,,,,,10025141,
mondo:0019558,discoid lupus erythematosus,['DLE'],,,90281,C0024138,,C26820,,D008179,,L93.0,10013072,
mondo:0019559,hypertrophic or verrucous lupus erythematosus,,,,90282,CN227653,,,,,,,,
mondo:0019560,lupus erythematosus tumidus,"['intermittent cutaneous lupus', 'tumid lupus erythematosus', 'let']",,,90283,C0406636,,C117112,,,,,,
mondo:0019561,lupus erythematosus panniculitis,"['lupus profundus', 'lupus erythematosus profundus', 'lupus panniculitis']",,,90285,C0030327,,C82884,,D015435,,,,
mondo:0019562,localized scleroderma,"['localized fibrosing scleroderma', 'localized morphoea', 'localised morphoea', 'localized scleroderma (disorder) [ambiguous]', 'morphea', 'Scleroderma, localized', 'Scleroderma, circumscribed or localised', 'circumscribed scleroderma', 'localised scleroderma (disorder) [ambiguous]', 'localized scleroderma', 'localised fibrosing scleroderma', 'localised morphea', 'Scleroderma, localised', 'Scleroderma, circumscribed or localized', 'localized morphea']",8472,,90289,C0036420,,C72069,,D012594,701.0,,10039712,
mondo:0019563,CREST syndrome,"['calcinosis - Raynaud phenomenon - esophageal involvement - sclerodactyly - telangiectasia', 'calcinosis, Raynaud^s phenomenon, esophageal dismobility, sclerodactyly, telangiectasia syndrome', 'limited cutaneous Systemic Scleroderma', 'calcinosis Raynaud phenomenon sclerodactyly telangiectasia', 'CRST syndromes', 'limited cutaneous Systemic sclerosis', 'calcinosis-Raynaud phenomenon-esophageal involvement-sclerodactyly-telangiectasia syndrome', 'phenomenon-sclerodactyly-telangiectasia, calcinosis-Raynaud', 'CRST syndrome', 'lcSSc', 'syndrome, CREST', 'calcinosis-Raynaud phenomenon-sclerodactyly-telangiectasia']",0060218,,90290,C0206138,,C70646,,D017675,,,10011380,
mondo:0019565,hereditary von Willebrand disease,"['von Willebrand disease', 'von Willebrand-Jrgens disease', 'vascular pseudohemophilia', 'von Willebrand^s disease', 'von Willebrand^s-Jurgens^ disease', 'vascular hemophilia', 'von Willebrand-Jurgens disease', 'von Willebrand disorder', 'hereditary von Willebrand disease (hereditary or acquired)', 'vascular haemophilia']",12531,,903,C0042974,"['-0.1029', '0.4062', '-0.5986', '0.2322', '-0.2576', '0.0398', '-0.103', '0.3633', '-0.1346', '-0.7866', '0.1737', '0.7036', '0.816', '0.88', '0.12274', '-0.4287', '0.1385', '0.03357', '-0.2', '-0.4705', '-0.3914', '-0.7397', '1.331', '0.2593', '-0.04456', '-0.2517', '-0.3335', '0.1437', '0.768', '0.07935', '0.8955', '-0.236', '0.4756', '0.373', '0.2455', '-0.506', '-0.5156', '-0.2052', '0.3694', '-0.2472', '0.9224', '-0.0415', '0.421', '-0.816', '0.491', '-0.0945', '-1.057', '0.2029', '0.1594', '-0.553', '0.6978', '-0.04654', '0.4414', '-0.1805', '-0.09064', '-0.1362', '-0.7397', '0.7085', '-0.9053', '-0.5063', '-0.559', '0.010254', '0.612', '-0.4202', '0.3198', '-0.000979', '0.1375', '-0.712', '-1.072', '0.3684', '-0.1753', '-0.0523', '-0.2102', '-0.829', '0.9175', '0.341', '1.02', '0.763', '0.413', '-0.1312', '-0.4917', '-0.28', '0.955', '-0.486', '0.02171', '0.1821', '0.1753', '0.4478', '-0.02275', '0.02942', '-0.309', '0.422', '0.0669', '-0.1195', '1.021', '0.435', '0.1333', '-0.996', '-0.4404', '0.167']",,,C531844,286.4,,10047715,
mondo:0019567,"Ehlers-Danlos syndrome, classic type, 1","['Ehlers-Danlos syndrome, type 1', 'type I Ehlers-Danlos syndrome', 'EDSCL1', 'Ehlers-Danlos syndrome, classic type, 1', 'EDS I', 'Ehlers-Danlos syndrome, type I']",14720,130000,90309,C0268335,"['0.393', '0.2788', '-0.7183', '0.356', '0.3008', '-0.8374', '0.0724', '0.3225', '-0.949', '0.5845', '0.09515', '-0.3403', '0.2686', '1.137', '-0.3533', '0.02087', '-0.652', '0.61', '0.01429', '-0.4287', '0.06934', '0.776', '0.3281', '0.1071', '-0.2094', '0.249', '0.192', '0.2136', '1.607', '0.3984', '0.9033', '-0.746', '0.0277', '-0.02592', '-0.08435', '0.145', '-0.4038', '0.06384', '0.48', '-1.118', '0.739', '-0.6055', '-0.6', '0.2712', '0.2455', '-0.6934', '-0.1686', '0.724', '1.197', '-0.4639', '0.10645', '-0.393', '0.509', '0.2377', '0.1283', '-0.4993', '-0.4658', '0.8403', '0.514', '-0.00303', '-0.1458', '0.5776', '0.2009', '-0.1154', '-0.02017', '0.5815', '-0.278', '0.7573', '-0.386', '1.134', '-0.512', '0.1039', '-0.471', '-0.6953', '-0.04257', '0.0001599', '-0.4453', '0.25', '0.1318', '-0.08356', '-0.577', '-0.569', '-0.001241', '0.382', '-0.4084', '-0.3547', '0.02428', '0.9194', '0.3083', '0.324', '0.4307', '0.1927', '-0.4246', '0.5303', '0.874', '0.3384', '0.4504', '-0.283', '-0.162', '-0.2325']",C125696,,C536194,,,,
mondo:0019568,"Ehlers-Danlos syndrome, classic type, 2","['EDS II, formerly', 'Ehlers Danlos syndrome, mitis type, formerly', 'Ehlers-Danlos syndrome, type Ii, formerly', 'Ehlers Danlos syndrome, mitis type', 'EDSCL2', 'Ehlers-Danlos syndrome, classic type, 2', 'Ehlers Danlos syndrome, mild Classic type', 'EDS II', 'Ehlers Danlos syndrome, mild Classic type, formerly', 'Ehlers-Danlos syndrome, type Ii']",0080726,130010,90318,C0268336,"['0.5713', '0.2656', '-0.658', '0.3625', '0.2292', '-0.7837', '0.1986', '0.3828', '-0.8027', '0.6973', '-0.07196', '-0.4373', '0.265', '1.262', '-0.3586', '0.09436', '-0.546', '0.6333', '-0.0634', '-0.3171', '0.1024', '0.6055', '0.261', '0.0649', '-0.3223', '0.01947', '-0.11304', '0.1808', '1.674', '0.335', '0.8374', '-0.5967', '0.004158', '-0.02754', '-0.0503', '0.2336', '-0.4194', '-0.05402', '0.54', '-1.114', '0.7856', '-0.643', '-0.5205', '0.2211', '0.2345', '-0.7866', '-0.2051', '0.739', '1.031', '-0.617', '0.1385', '-0.3462', '0.6445', '0.2006', '0.2388', '-0.3245', '-0.4102', '0.8276', '0.4219', '0.069', '-0.1043', '0.4954', '0.2637', '-0.2113', '-0.0378', '0.4004', '-0.5264', '0.766', '-0.4617', '1.123', '-0.4915', '0.1642', '-0.498', '-0.6465', '0.006084', '0.1719', '-0.4836', '0.4106', '0.02342', '-0.1682', '-0.6094', '-0.4348', '0.001706', '0.2358', '-0.682', '-0.2224', '-0.06805', '0.7915', '0.438', '0.4038', '0.4268', '0.1696', '-0.3281', '0.4504', '0.6104', '0.299', '0.2012', '-0.3923', '-0.02591', '-0.2778']",C125697,,C536195,,,,
mondo:0019569,Cockayne syndrome type 1,"['Cockayne syndrome caused by mutation in ERCC8', 'CSA', 'Cockayne syndrome classic form', 'ERCC8 Cockayne syndrome', 'Cockayne syndrome, type A', 'Cockayne syndrome type a', 'Cockayne syndrome A', 'Cockayne syndrome type A', 'Cockayne syndrome type I', 'Cockayne syndrome classical']",0080907,216400,90324,C0751039,,C135725,,,,,,
mondo:0019570,Cockayne syndrome type 2,"['Cockayne syndrome type 2', 'CSB', 'Cockayne syndrome, type B', 'Cockayne syndrome B', 'Cockayne syndrome type II', 'Cockayne syndrome type B']",0080908,133540,90324,C0751038,"['-0.2976', '0.3328', '0.1285', '-0.01', '0.2097', '-0.3796', '-0.10815', '0.02045', '-0.3384', '-0.291', '0.03348', '0.1974', '0.2878', '-0.1243', '-0.1019', '-0.1445', '-0.1764', '-0.3596', '-0.00645', '-0.3237', '0.1484', '-0.2166', '0.259', '0.05304', '0.2157', '0.137', '-0.0741', '0.1114', '0.1655', '-0.06195', '-0.02179', '0.2095', '0.4167', '-0.0785', '0.1665', '-0.247', '0.05634', '-0.09735', '-0.04977', '-0.4475', '0.2488', '-0.3845', '0.1819', '0.0873', '-0.1533', '-0.429', '-0.04608', '0.0908', '0.6025', '-0.1475', '-0.121', '-0.3132', '-0.1134', '0.2129', '-0.1372', '-0.1943', '0.5493', '0.03497', '-0.486', '0.2747', '0.2698', '0.1951', '0.04446', '0.05847', '0.2222', '0.03072', '0.296', '-0.08167', '-0.1895', '0.2197', '-0.4573', '-0.01481', '-0.012634', '0.05023', '0.1478', '0.1796', '0.05493', '0.1153', '-0.314', '-0.09546', '0.159', '0.1179', '-0.3179', '0.1211', '-0.2776', '0.02574', '0.3875', '0.5615', '0.2898', '0.1069', '0.12445', '0.11725', '-0.07947', '-0.2717', '0.485', '0.1418', '0.312', '-0.632', '0.002949', '0.09827']",C135726,,,,,,
mondo:0019571,autosomal dominant cutis laxa,"['ADCL', 'cutis laxa, autosomal dominant']",0070142,,90348,C0268350,"['0.2052', '-0.3416', '-0.3057', '-0.6025', '0.3926', '-0.65', '0.19', '0.304', '-0.5884', '-0.1733', '-0.3396', '-0.5366', '-0.6025', '-0.06256', '-0.3083', '0.5537', '-0.01913', '0.04858', '-0.65', '-0.8066', '-0.5034', '-0.1582', '0.442', '-0.1769', '-0.3484', '0.1561', '0.0825', '0.2441', '0.696', '-0.3716', '0.822', '0.04526', '0.467', '0.493', '0.0106', '-0.4756', '-0.4177', '-0.3389', '0.7144', '-0.1238', '0.405', '-0.4453', '0.4429', '0.1921', '0.4224', '-0.0996', '-0.299', '0.331', '-0.2546', '-0.4187', '0.1409', '0.241', '0.3513', '0.5347', '-0.8633', '0.02328', '-0.08386', '0.1871', '-0.156', '-0.533', '0.603', '0.2961', '-0.2974', '-0.336', '0.303', '-0.309', '0.4883', '0.3337', '-0.4731', '0.725', '-0.935', '-0.005146', '-0.3604', '-0.0763', '0.3672', '-0.2544', '0.1309', '0.3792', '-0.05508', '-0.655', '-0.1255', '-0.07996', '-0.015236', '0.2698', '-0.0452', '0.3684', '-0.02481', '-0.09503', '-0.1912', '-0.05142', '0.6094', '-0.1301', '0.1346', '-0.2979', '0.797', '-0.1237', '0.792', '-0.3582', '-0.01369', '0.2705']",,,C562627,,,,
mondo:0019572,autosomal recessive cutis laxa type 1,"['autosomal recessive cutis laxa, pulmonary emphysema type', 'cutis laxa, type 1', 'ARCL1', 'autosomal recessive cutis laxa type I', 'cutis laxa, autosomal recessive type 1', 'autosomal recessive cutis laxa type 1', 'autosomal recessive cutis laxa with severe systemic involvement']",0070144,,90349,CN206407,"['0.5557', '-0.2576', '-0.206', '-0.6104', '0.574', '-0.7153', '0.39', '0.71', '-0.81', '-0.0712', '-0.3792', '-0.1188', '0.10095', '0.1757', '-0.7363', '0.55', '0.3403', '-0.1355', '-0.4766', '-0.388', '-0.5283', '-0.0778', '0.3096', '-0.413', '-0.5806', '-0.19', '-0.0169', '0.2496', '0.4827', '-0.0729', '0.692', '0.1718', '0.3892', '0.1965', '0.1495', '-0.0806', '-0.13', '-0.3767', '0.1515', '-0.159', '0.1823', '-0.298', '0.3079', '0.513', '0.2622', '0.2235', '0.0708', '0.525', '-0.1738', '-0.1887', '-0.0871', '0.4275', '0.9634', '0.11536', '-0.781', '-0.1885', '-0.325', '0.3535', '-0.1823', '-0.4128', '0.1006', '0.3215', '-0.2866', '-0.07', '0.51', '-0.4722', '0.5366', '0.2148', '-0.683', '0.5986', '-0.3274', '-0.2905', '-0.276', '0.02713', '-0.08514', '-0.05234', '-0.1897', '0.03026', '-0.3418', '-0.461', '-0.1255', '-0.2256', '-0.1775', '0.4485', '-0.229', '0.4844', '0.2954', '-0.2073', '-0.0001926', '-0.09045', '0.432', '0.4407', '0.06744', '-0.03418', '0.7246', '0.1678', '0.9663', '-0.07117', '0.0874', '0.1597']",,,C536225,,,,
mondo:0019573,autosomal recessive cutis laxa type 2,"['ARCL2', 'cutis laxa with joint laxity and developmental delay']",,,90350,,"['0.458', '0.1445', '0.06058', '-0.403', '0.7627', '-0.714', '-0.1947', '0.7354', '-0.837', '0.12305', '-0.4946', '-0.4756', '-0.0508', '0.04803', '-0.0983', '0.4187', '0.8164', '-0.1249', '-0.4197', '-0.77', '-0.1768', '-0.0971', '0.209', '-0.4565', '-0.313', '-0.2338', '0.005737', '-0.06094', '0.663', '-0.08344', '0.948', '-0.2123', '0.5933', '0.4639', '-0.2396', '-0.177', '-0.1329', '-0.1127', '0.0501', '-0.0791', '0.3704', '-0.8447', '-0.2399', '0.37', '0.1559', '0.07697', '-0.1285', '0.3923', '-0.1675', '-0.1081', '0.4636', '-0.1377', '-0.0676', '0.3286', '-0.453', '-0.09174', '-0.5083', '0.4536', '-0.1782', '-0.2261', '0.256', '-0.235', '-0.49', '0.11743', '0.3562', '-0.1335', '-0.153', '0.03778', '-0.3655', '0.8315', '-0.2964', '0.1832', '-0.1327', '0.085', '0.3923', '0.1351', '-0.1935', '-0.489', '0.061', '-0.3008', '-0.03754', '-0.2717', '-0.5923', '0.666', '-0.3645', '0.6606', '-0.0664', '0.06244', '-0.0786', '0.343', '0.535', '0.5723', '0.4802', '0.004704', '0.673', '0.3337', '0.448', '-0.1544', '0.2632', '0.0927']",,,,,,,
mondo:0019574,secondary intestinal lymphangiectasia,,,,90363,C4273969,,,,,,,,
mondo:0019575,hypotrichosis simplex of the scalp,['hereditary hypotrichosis simplex of the scalp'],,,90368,,"['-0.2463', '0.3735', '-0.0738', '0.1959', '0.3655', '-1.209', '0.04312', '0.5327', '-0.3008', '-0.49', '-0.5293', '-0.01446', '-0.3384', '0.01551', '-0.0913', '0.2135', '0.6235', '-0.591', '-0.2498', '-0.612', '-0.5596', '-0.04898', '0.0964', '-0.08075', '0.4834', '0.2048', '-0.669', '0.4346', '-0.0723', '0.2129', '0.814', '0.00556', '-1.054', '0.03595', '0.433', '-0.11237', '-0.254', '-0.2455', '-0.02623', '-0.0396', '0.6357', '-0.3445', '0.1616', '-0.3225', '0.2988', '-0.2499', '-0.12177', '-0.1523', '-0.0732', '-0.1887', '0.2218', '-0.0737', '0.468', '-0.3809', '-0.2086', '-0.4834', '0.4211', '-0.10535', '-0.2297', '-0.317', '-0.005314', '-0.1897', '0.2336', '0.3345', '0.2388', '0.2389', '0.5664', '0.3855', '-0.0647', '0.8794', '0.1268', '-0.5054', '0.1821', '0.07294', '-0.2316', '0.535', '-0.0846', '0.3667', '0.01808', '-0.09985', '0.4922', '0.4634', '0.587', '0.2079', '-0.159', '-0.2627', '-0.08923', '0.2373', '0.09906', '0.2556', '0.07117', '1.195', '0.734', '0.1948', '0.8433', '0.2014', '0.2438', '-0.2556', '0.536', '0.1965']",,,,,,,
mondo:0019576,telangiectasia macularis eruptiva perstans,,,,90389,C0263402,,,,,448.9,,10043192,
mondo:0019577,anonychia-onychodystrophy syndrome,,,,90390,C1862840,,,,C536378,,,,
mondo:0019578,nodular lichen myxedematosus,['atypical tuberous myxedema of Jadassohn-Dosseker'],,,90393,C4273968,,,,,,,,
mondo:0019579,discrete papular lichen myxedematosus,,,,90394,C4273967,,,,,,,,
mondo:0019580,papular mucinosis of infancy,['cutaneous mucinosis of infancy'],,,90395,C4273966,,,,,,,,
mondo:0019581,acral persistent papular mucinosis,,,,90396,C0406660,,,,,701.8,,,
mondo:0019582,self-healing papular mucinosis,,,,90397,,,,,,,,,
mondo:0019583,localized lichen myxedematosus with mixed features of different subtypes,,,,90398,,,,,,,,,
mondo:0019584,localized lichen myxedematosus with monoclonal gammopathy or systemic symptoms,,,,90399,,,,,,,,,
mondo:0019585,scleromyxedema without monoclonal gammopathy,,,,90400,,,,,,,,,
mondo:0019586,X-linked nonsyndromic hearing loss,"['X-linked isolated neurosensory deafness type DFN', 'X-linked isolated neurosensory hearing loss type DFN', 'X-linked non-syndromic sensorineural deafness type DFN', 'nonsyndromic genetic deafness, X-linked', 'X-linked nonsyndromic genetic deafness', 'X-linked deafness', 'X-linked isolated sensorineural deafness type DFN', 'X-linked non-syndromic sensorineural hearing loss type DFN', 'X-linked non-syndromic neurosensory hearing loss type DFN', 'X-linked isolated sensorineural hearing loss type DFN', 'X-linked non-syndromic neurosensory deafness type DFN', 'nonsyndromic deafness, X-linked']",0050566,,90625,CN206422,"['-0.0398', '0.153', '0.1384', '-0.082', '0.1671', '-0.2162', '-0.04492', '0.1997', '-0.1167', '-0.1403', '-0.15', '-0.1758', '-0.0988', '-0.03928', '-0.0749', '-0.1593', '0.1229', '-0.0372', '-0.04337', '-0.2993', '-0.07025', '-0.04153', '0.1476', '-0.03983', '0.1552', '0.0887', '-0.1215', '-0.1814', '0.2051', '-0.1263', '0.11017', '0.1543', '0.2153', '0.1393', '-0.0791', '-0.196', '-0.11774', '-0.319', '-0.1396', '-0.2096', '0.0642', '-0.2137', '0.10956', '-0.0909', '-0.03152', '-0.2118', '-0.08014', '0.02336', '0.03195', '0.09375', '0.0425', '-0.1023', '0.0134', '-0.1971', '-0.08685', '-0.1715', '0.2018', '-0.1461', '-0.1768', '0.10504', '0.0558', '-0.0627', '0.05347', '0.11285', '-0.08044', '-0.01558', '0.03586', '0.262', '-0.2229', '0.2798', '-0.3186', '0.0425', '0.1476', '-0.2444', '0.151', '0.0598', '0.09015', '0.03238', '-0.1796', '-0.0516', '0.06125', '-0.09094', '-0.078', '0.29', '-0.001678', '-0.03427', '0.0265', '0.2815', '-0.0345', '0.1919', '0.147', '0.4075', '0.1283', '0.117', '0.4202', '-0.00741', '0.3284', '-0.3884', '0.1328', '0.0884']",,,,,,,
mondo:0019587,autosomal dominant nonsyndromic hearing loss,"['autosomal dominant nonsyndromic hearing loss and deafness', 'autosomal dominant isolated sensorineural deafness type DFNA', 'autosomal dominant isolated deafness', 'autosomal dominant isolated sensorineural hearing loss type DFNA', 'autosomal dominant non-syndromic neurosensory deafness type DFNA', 'autosomal dominant non-syndromic sensorineural deafness type DFNA', 'autosomal dominant nonsyndromic genetic deafness', 'autosomal dominant deafness', 'nonsyndromic deafness, autosomal dominant', 'nonsyndromic genetic deafness, autosomal dominant', 'autosomal dominant isolated neurosensory hearing loss type DFNA', 'autosomal dominant isolated neurosensory deafness type DFNA', 'deafness, autosomal dominant', 'autosomal dominant nonsyndromic hearing impairment', 'autosomal dominant nonsyndromic deafness', 'autosomal dominant non-syndromic sensorineural hearing loss type DFNA', 'autosomal dominant non-syndromic neurosensory hearing loss type DFNA']",0050564,,90635,CN043649,"['-0.004513', '0.0518', '0.01845', '-0.02129', '0.02112', '-0.05957', '0.009895', '0.072', '-0.04346', '-0.04895', '-0.03253', '-0.02158', '-0.0158', '0.008965', '-0.01605', '-0.0187', '0.0006647', '-0.0367', '-0.02017', '-0.1168', '-0.0357', '-0.01903', '0.0434', '-0.02386', '0.02118', '0.014244', '-0.03403', '-0.03035', '0.008705', '-0.04495', '0.0416', '0.000305', '0.0515', '0.0364', '-0.01637', '-0.0282', '-0.02151', '-0.04022', '-0.013', '-0.06696', '0.02188', '-0.05804', '0.02061', '-0.01562', '-0.00637', '-0.07495', '-0.03418', '0.0451', '0.01791', '0.0201', '0.01013', '-0.02052', '0.01111', '-0.013626', '-0.02753', '-0.05383', '0.0489', '-0.014725', '-0.0762', '0.010704', '0.03128', '0.001922', '0.01542', '0.01509', '-0.001385', '0.01567', '0.04996', '0.0691', '-0.0614', '0.0884', '-0.08453', '0.01255', '0.02473', '-0.04758', '0.05698', '0.03333', '0.01587', '-0.005016', '-0.04678', '-0.02759', '-0.006557', '-0.002157', '-0.01888', '0.06476', '-0.00516', '0.01666', '0.02678', '0.05896', '0.04608', '0.0393', '0.02704', '0.07117', '0.00455', '0.02713', '0.1458', '0.05106', '0.0854', '-0.0906', '-0.001456', '0.02237']",,,,,,,
mondo:0019588,"hearing loss, autosomal recessive","['nonsyndromic deafness, autosomal recessive', 'autosomal recessive nonsyndromic genetic deafness', 'deafness, neurosensory nonsyndromic recessive, DFN', 'autosomal recessive nonsyndromic deafness', 'autosomal recessive isolated sensorineural deafness type DFNB', 'autosomal recessive isolated neurosensory deafness type DFNB', 'nonsyndromic genetic deafness, autosomal recessive', 'autosomal recessive non-syndromic sensorineural deafness type DFNB', 'deafness, autosomal recessive', 'autosomal recessive non-syndromic neurosensory deafness type DFNB']",0050565,607197,90636,CN206424,"['-0.02254', '0.0719', '0.03128', '-0.014946', '0.05133', '-0.0867', '0.003614', '0.07025', '-0.04123', '-0.04648', '-0.03616', '-0.02402', '-0.005116', '0.01816', '-0.00847', '-0.02751', '0.01374', '-0.04434', '-0.04376', '-0.1508', '-0.04214', '-0.0319', '0.04758', '-0.0308', '0.02681', '0.01312', '-0.009285', '-0.03796', '0.04025', '-0.03757', '0.05008', '0.00866', '0.0798', '0.0442', '-0.02328', '-0.0349', '-0.02194', '-0.0428', '-0.003544', '-0.08545', '0.02032', '-0.0819', '0.0562', '-0.013954', '0.006588', '-0.09686', '-0.0289', '0.04688', '0.0373', '0.03375', '0.01482', '-0.0322', '-0.003485', '-0.0172', '-0.0383', '-0.0586', '0.0826', '-0.02414', '-0.08496', '0.02359', '0.05194', '0.01325', '0.02191', '0.01775', '-0.01059', '0.003157', '0.07495', '0.0682', '-0.0723', '0.0945', '-0.1173', '0.007626', '0.02924', '-0.0651', '0.04782', '0.0525', '0.0287', '0.001466', '-0.0653', '-0.037', '0.01557', '-0.0163', '-0.03235', '0.089', '0.02014', '0.014275', '0.02179', '0.05722', '0.04913', '0.03546', '0.02249', '0.0958', '0.02853', '0.0384', '0.1637', '0.065', '0.10315', '-0.1201', '0.005836', '0.03317']",,,C564609,,,,
mondo:0019591,panhypopituitarism,"['Simmonds^ disease', 'Simmond^s disease', 'complete hypopituitarism']",9410,,90695,C0242343,"['-0.771', '-0.1545', '-0.02348', '-0.2096', '0.167', '0.4524', '0.095', '-0.02614', '-0.3203', '-0.4473', '0.3354', '0.0331', '0.04837', '0.732', '-0.4465', '-0.3777', '-0.006184', '0.5044', '-0.8696', '-0.4053', '-0.06995', '-0.1881', '-0.0403', '-0.347', '0.1214', '0.249', '-0.2228', '-0.2396', '-0.475', '0.3025', '0.5093', '0.04938', '0.865', '0.09406', '0.04745', '0.512', '-0.4163', '0.311', '-0.02574', '0.5156', '0.3452', '-0.1459', '-0.2554', '-0.5312', '0.3162', '-0.4966', '0.3667', '-0.1373', '0.8086', '0.582', '-0.3062', '0.3674', '-0.0003839', '-0.0133', '-0.1', '0.4983', '0.2438', '-0.03198', '-0.2267', '0.03418', '-0.05298', '0.4084', '-0.2512', '-0.2964', '-0.4783', '0.6396', '0.4404', '0.502', '-0.3203', '-0.03787', '-0.4685', '0.4133', '0.073', '-0.649', '0.4365', '0.1973', '-0.4043', '0.2712', '0.342', '0.3477', '0.0158', '0.287', '-0.0879', '-0.2573', '0.2144', '-0.0669', '0.2517', '-0.2137', '0.9062', '0.128', '-0.0806', '0.7886', '0.00533', '-0.268', '1.144', '0.166', '-0.634', '-0.2537', '0.1076', '0.3196']",C110940,,,253.2,,10033662,
mondo:0019593,"46,XX disorder of sex development induced by fetal androgens excess","['46,XX DSD induced by fetal androgens excess', '46,XX DSD induced by foetal androgens excess']",,,90776,CN227655,,,,,,,,
mondo:0019597,"46,XY disorder of sex development due to isolated 17,20-lyase deficiency",,,,90796,CN206443,"['-0.39', '0.02162', '-0.002966', '-0.3113', '0.2861', '-0.08563', '-0.1892', '0.4146', '-0.2255', '-0.1901', '-0.02036', '-0.252', '-0.02087', '0.11475', '-0.1964', '-0.10596', '0.6543', '0.2983', '-0.319', '-0.5386', '-0.346', '-0.1733', '0.5093', '-0.01651', '0.1803', '-0.184', '0.0519', '0.2395', '0.01436', '-0.4036', '0.3997', '-0.02298', '0.6055', '0.1731', '-0.3584', '-0.2224', '0.2249', '-0.00846', '0.06976', '-0.4111', '0.4116', '-0.001611', '-0.0656', '-0.2026', '-0.203', '-0.553', '0.1337', '0.08795', '-0.04996', '0.346', '-0.10266', '-0.373', '-0.2198', '0.1517', '-0.3328', '0.611', '0.3228', '-0.4866', '-0.4512', '-0.002453', '-0.03415', '0.4248', '0.1182', '0.1681', '-0.03378', '0.1608', '0.2969', '0.4263', '-0.3787', '0.0854', '-0.3', '0.3416', '0.001166', '-0.0635', '-0.2244', '-0.4956', '0.0278', '0.03607', '-0.5283', '-0.3306', '-0.1072', '0.4797', '0.0491', '0.02402', '0.0003572', '-0.00969', '-0.1284', '-0.3667', '0.2363', '-0.3206', '-0.02971', '0.5576', '-0.269', '-0.2164', '0.497', '-0.164', '-0.0349', '-0.3154', '-0.0811', '0.3062']",,,,,,,
mondo:0019599,primary lipodystrophy,,,,90970,,,,,,,,,
mondo:0019600,xeroderma pigmentosum,"['angioma pigmentosum atrophicum', 'atrophoderma pigmentosum', 'XP', 'melanosis lenticularis progressiva', 'xeroderma of Kaposi', 'pigmented epitheliomatosis', 'Kaposi disease', 'Kaposi dermatosis', 'xeroderma pigmentosa', 'xeroderma pigmentosum syndrome']",0050427,,910,C0043346,"['0.2421', '0.3694', '-0.6504', '0.02667', '0.453', '-0.209', '0.1348', '0.3555', '-0.1254', '-0.08765', '0.8066', '0.5156', '-0.11707', '0.3772', '0.1577', '-0.2224', '0.3682', '-0.485', '-0.0773', '-0.12305', '-0.2496', '-0.4124', '-0.0683', '-0.1068', '-0.0005116', '0.4304', '-0.4788', '0.3062', '-0.8716', '-0.1676', '0.4224', '0.04477', '0.4075', '0.11224', '-0.0796', '0.362', '-0.4536', '-0.8916', '-0.2203', '-0.2318', '0.03186', '-0.687', '0.3228', '-0.4666', '0.1045', '-0.06216', '-0.0501', '-0.295', '0.1326', '0.0937', '0.1818', '-0.3628', '-0.06696', '-0.0281', '-0.555', '0.113', '0.4414', '0.412', '-0.637', '-0.4062', '0.1016', '-0.3118', '-0.442', '0.601', '-0.1506', '0.2189', '0.07153', '0.2634', '0.03075', '0.362', '-0.406', '0.1942', '-0.07043', '0.1534', '0.9106', '0.05', '0.3335', '-0.4282', '0.4727', '-0.4236', '0.3044', '-0.295', '-0.229', '0.4153', '0.05875', '-0.2832', '0.2289', '0.645', '0.4353', '0.1012', '0.9634', '0.3843', '-0.01755', '-0.284', '0.3027', '0.10315', '0.2156', '-0.1377', '-0.3506', '0.1865']",C3452,,D014983,,Q82.1,10048220,
mondo:0019603,osteopenia-myopia-hearing loss-intellectual disability-facial dysmorphism syndrome,,,,91133,CN206455,,,,,,,,
mondo:0019604,acquired monoclonal Ig light chain-associated Fanconi syndrome,"['acquired Fanconi syndrome secondary to monoclonal gammopathy', 'acquired monoclonal immunoglobulin light chain-associated Fanconi syndrome']",,,91136,CN206457,,,,,,,,
mondo:0019605,immunotactoid or fibrillary glomerulopathy,"['Immunotactoid or fibrillary glomerulonephritis', 'fibrillary glomerulonephritis and immunotactoid glomerulopathy']",,,91137,,,,,,,,,
mondo:0019606,simple cryoglobulinemia,['cryoglobulinemia type 1'],,,91139,CN206459,,,,,,D89.1,,
mondo:0019607,unspecified juvenile idiopathic arthritis,['unspecified JIA'],,,91140,,,,,,,,,
mondo:0019608,"46,XX disorder of sex development induced by maternal-derived androgen","['46,XX DSD induced by maternal-derived androgen']",,,91144,CN227662,,,,,,,,
mondo:0019609,Zellweger spectrum disorders,"['congenital iron overload', 'Zellweger syndrome', 'ZWS', 'Zellweger leukodystrophy', 'Zellweger spectrum disorders', 'ZS', 'cerebrohepatorenal syndrome']",905,,912,C0043459,"['0.03537', '0.3525', '0.3044', '-0.4878', '-0.01242', '-0.4453', '-0.2275', '0.9365', '-0.404', '-0.0449', '-0.333', '-0.577', '-0.1101', '0.2135', '-0.7563', '-0.8037', '0.3867', '-0.2969', '-0.61', '-0.02995', '0.3657', '-0.9834', '0.423', '0.1637', '0.03256', '0.01424', '-0.457', '0.04523', '-0.0595', '-0.2238', '0.4075', '-0.3435', '0.2651', '0.2893', '0.115', '0.04675', '0.09094', '-0.2434', '0.4714', '-0.1936', '-0.5103', '-0.265', '0.02556', '-0.09436', '-0.5586', '-0.1018', '0.2703', '-0.009346', '-0.11816', '0.2325', '-0.1564', '-0.1685', '0.0909', '-0.4497', '-0.3599', '0.05017', '0.3262', '-0.2776', '-0.5024', '0.696', '0.2864', '-0.533', '0.514', '0.4023', '-0.1083', '0.2585', '0.4126', '0.1349', '-0.12036', '0.4365', '-0.3274', '0.4', '-0.2363', '0.4597', '-0.597', '0.5957', '0.5933', '-0.727', '-0.5806', '-0.3047', '-0.0246', '-0.2666', '-1.074', '0.5366', '-0.4255', '0.4072', '0.1431', '-0.216', '0.1683', '0.4756', '0.2637', '0.5703', '0.2203', '0.513', '-0.2223', '-0.2037', '0.644', '-0.01112', '0.556', '0.1575']",C85239,,D015211,,E71.510,,
mondo:0019610,Zollinger-Ellison syndrome,"['Zollinger-Ellison syndrome', 'Zollinger Ellison syndrome', 'gastrinoma', 'pancreatic ulcerogenic tumour syndrome', 'Zollinger-Ellison syndrome (disease)', 'Z E syndrome', 'pancreatic ulcerogenic tumor syndrome', 'ZES']",0050782,,913,C0043515,,C3453,0007549,D015408,,C25.4,10017852,0002044
mondo:0019611,TSH-secreting pituitary adenoma,"['TSH secreting adenoma of the pituitary gland', 'TSH-oma', 'thyroid stimulating hormone producing adenoma of the pituitary gland', 'thyroid stimulating hormone secreting pituitary gland adenoma', 'TSH secreting pituitary adenoma', 'TSH producing adenoma of the pituitary gland', 'thyroid stimulating hormone secreting adenoma of the pituitary gland', 'TSH secreting adenoma of the pituitary', 'TSH producing adenoma of pituitary gland', 'thyrotroph adenoma', 'thyroid stimulating hormone secreting adenoma of pituitary', 'thyrotropin producing pituitary gland adenoma', 'TSH producing adenoma of pituitary', 'TSH secreting adenoma of pituitary', 'thyrotropinoma', 'thyroid stimulating hormone producing adenoma of the pituitary', 'TSH producing pituitary adenoma', 'TSH-producing adenoma', 'TSH producing pituitary gland adenoma', 'thyroid stimulating hormone producing pituitary gland adenoma', 'thyrotrophic adenoma', 'thyroid stimulating hormone-producing adenoma', 'TSH secreting adenoma of pituitary gland', 'pituitary thyrotrophic adenoma', 'thyroid stimulating hormone producing adenoma of pituitary', 'TSH producing adenoma of the pituitary', 'TSH secreting pituitary gland adenoma', 'thyrotrope adenoma', 'thyroid stimulating hormone producing pituitary adenoma', 'thyroid stimulating hormone-secreting pituitary adenoma', 'thyroid stimulating hormone producing adenoma of pituitary gland', 'thyroid stimulating hormone secreting adenoma of pituitary gland', 'thyroid stimulating hormone secreting pituitary adenoma', 'thyroid stimulating hormone secreting adenoma of the pituitary', 'TSH-producing pituitary gland adenoma', 'TSHoma']",,,91347,C0346303,,C8011,,,,D35.2,,
mondo:0019612,functioning gonadotropic adenoma,"['gonadotroph adenoma', 'functioning pituitary gonadotropic adenoma']",,,91348,C0346304,,,,,,D35.2,,
mondo:0019613,non-functioning pituitary adenoma,"['functionless pituitary gland adenoma', 'silent pituitary gland adenoma', 'non-functioning pituitary gland adenoma', 'non-secretory adenoma of pituitary', 'non-secretory adenoma of pituitary gland', 'non-functioning adenoma of pituitary', 'functionless adenoma of the pituitary', 'non-secretory pituitary adenoma', 'non-functioning adenoma of pituitary gland', 'non-functioning pituitary adenoma', 'non-functioning adenoma of the pituitary gland', 'functionless adenoma of the pituitary gland', 'functionless pituitary adenoma', 'non-functioning adenoma of the pituitary', 'NFPA', 'nonfunctional pituitary gland adenoma', 'functionless adenoma of pituitary', 'non-secretory adenoma of the pituitary', 'non-secretory adenoma of the pituitary gland', 'functionless adenoma of pituitary gland', 'non-secretory pituitary gland adenoma']",5715,,91349,,,C4348,0008516,,,D35.2,,
mondo:0019614,pituitary deficiency due to Rathke^s pouch cysts,['pituitary deficiency due to Rathke^s cleft cysts'],,,91350,,,,,,,E23.0,,
mondo:0019615,pituitary dermoid and epidermoid cysts,,,,91351,,,,,,,,,
mondo:0019617,pituitary deficiency due to empty sella turcica syndrome,['hypopituitarism due to empty sella turcica syndrome'],,,91354,CN206468,,,,,,E23.0,,
mondo:0019618,Sheehan syndrome,"['postpartum pituitary necrosis', 'Sheehan^s syndrome', 'postpartum hypopituitarism', 'postpartum panhypopituitarism', 'postpartum panhypopituitary syndrome']",9476,,91355,C0242342,,C35300,,D007018,,E23.0,10036297,
mondo:0019619,duplication of the esophagus,,,,91357,,,,,,,,,
mondo:0019620,congenital esophageal diverticulum,['congenital esophageal pouch'],,,91358,,,,,,750.4,,,
mondo:0019621,chronic pneumonitis of infancy,['CPI'],,,91359,CN206472,,,,,,,,
mondo:0019622,non-specific interstitial pneumonia,"['NSIP', 'non-specific idiopathic interstitial pneumonia', 'nonspecific interstitial pneumonia']",2801,,91364,C1290344,,C35717,,,516.8,,,
mondo:0019623,hereditary angioedema,"['hereditary angioneurotic edema', 'hereditary angioneurotic oedema', 'HAE', 'deficiency of C1 esterase inhibitor', 'hereditary non histamine-induced angioedema', 'hereditary bradykinine-induced angioedema', 'familial angioneurotic oedema', 'familial angioneurotic edema', 'angioedema, hereditary', 'HANE', 'hereditary angioedema']",14735,,91378,CN239191,"['0.4827', '0.03952', '-0.9453', '-0.02579', '-0.595', '-0.0656', '0.4797', '0.2352', '-0.3877', '0.2079', '-0.1809', '0.08264', '0.1431', '0.0993', '-0.758', '0.01234', '0.0763', '-0.663', '-0.2411', '-0.5776', '0.03595', '-0.2732', '0.8643', '-0.1443', '-0.2366', '-0.07416', '0.399', '0.2454', '0.2183', '-0.3076', '0.612', '0.0667', '0.03702', '0.3813', '-0.193', '0.1322', '-0.11926', '0.1797', '-0.2235', '0.4475', '0.2091', '-0.4895', '0.1992', '-0.486', '-0.1206', '0.2235', '-0.562', '-0.3755', '0.1715', '0.5664', '-0.3848', '-0.1185', '0.529', '-0.05972', '-0.229', '0.10425', '0.2888', '-0.546', '-0.4973', '-0.03302', '-0.1466', '0.1593', '0.09094', '-0.3586', '0.552', '0.374', '0.5396', '0.12134', '-0.1366', '0.4453', '0.0385', '-0.259', '-0.294', '-0.06433', '0.5977', '0.03522', '0.3306', '-0.07996', '0.2339', '-0.2052', '-0.5073', '0.05548', '-0.0896', '-0.0379', '0.1373', '-0.0791', '0.1724', '0.49', '-0.02286', '-0.524', '0.2942', '0.0966', '0.1252', '-0.1147', '0.745', '-0.05142', '0.2316', '-0.578', '-0.3699', '0.311']",C84758,,D054179,,,10019860,
mondo:0019624,acquired angioedema,"['AAE', 'acquired non histamine-induced angioedema', 'acquired angioneurotic oedema', 'acquired angioedema', 'acquired C1 inhibitor deficiency', 'acquired bradykinine-induced angioedema', 'angioedema, acquired', 'acquired angioneurotic edema']",0080941,,91385,C2931758,,,,C538173,,,,
mondo:0019625,familial thoracic aortic aneurysm and aortic dissection,"['familial thoracic aortic aneurysm and dissection', 'Erdheim disease', 'FTAAD', 'familial thoracic aortic aneurysm', 'familial aortic dissection', 'cystic medial necrosis of aorta', 'familial TAAD', 'Erdheim cystic medial necrosis of aorta', 'familial aortic aneurysm', 'annuloaortic ectasia']",,,91387,CN118826,,,,,447.9,,,
mondo:0019626,isolated ankyloblepharon filiforme adnatum,,,,91397,C1302999,,,,,,,,
mondo:0019627,isolated congenital alacrima,['nonsyndromic congenital alacrima'],,,91416,C4273963,,,,,,,,
mondo:0019628,Rieger anomaly,,,,91483,,,,,,,,10059198,
mondo:0019629,sclerocornea,"['isolated congenital sclerocornea', 'sclerocornea', 'sclerocornea (disease)']",0060252,,91490,,,,,C565209,,,,0000647
mondo:0019630,congenital ectropion uveae,,,,91491,,,,,,,Q10.1,,
mondo:0019631,persistent hyperplastic primary vitreous,"['persistent foetal vasculature syndrome', 'ncRNA disease', 'PFVS', 'congenital retinal detachment', 'persistent fetal vasculature syndrome', 'PHPV', 'non-syndromic congenital retinal non-attachment']",0060282,,91495,,"['-0.4133', '0.1842', '0.23', '-0.1516', '-0.01511', '0.1584', '0.1716', '-0.1495', '-0.683', '0.1459', '-0.12494', '-0.499', '-0.3328', '-0.1288', '-0.7666', '-0.3435', '0.011', '-0.2698', '0.389', '-0.4915', '-0.0725', '-0.08594', '0.2008', '-0.344', '0.2837', '0.353', '-0.137', '0.3755', '-0.01938', '0.3054', '0.2192', '-0.1096', '0.4387', '0.2281', '0.10614', '0.38', '-0.07025', '-0.1227', '-0.3757', '-0.563', '0.1571', '0.1846', '0.324', '-0.02339', '-0.333', '0.0494', '0.1055', '-0.10345', '0.2325', '0.05603', '0.2317', '-0.1819', '-0.05444', '-0.3135', '-0.2703', '-0.3086', '0.5776', '-0.03595', '-0.5713', '-0.1564', '0.22', '-0.09686', '-0.2556', '0.384', '-0.1486', '-0.352', '0.66', '0.4077', '-0.4705', '0.2399', '-0.382', '0.4229', '0.1827', '0.0317', '-0.06525', '-0.09015', '-0.07947', '0.4214', '-0.5815', '-0.1978', '-0.09094', '0.11633', '0.0468', '0.5254', '-0.07275', '-0.4885', '0.1805', '0.0915', '-0.03384', '-0.3025', '0.1376', '0.5596', '0.1482', '0.2625', '0.8623', '-0.504', '0.4734', '-0.2832', '0.02914', '0.1025']",C161554,,D054514,,,,
mondo:0019632,Lyme disease,"['neurological Lyme disease', 'neuroborreliosis', 'Borrelia', 'Borreliella burgdorferi caused disease or disorder', 'Lyme borreliosis', 'Lyme neuroborreliosis', 'Borrelia burgdorferi infection', 'Bannworth^s syndrome', 'Lyme disease', 'Bannwarth syndrome']",11729,,91546,C0024198,,C45161,0008510,D008193,088.81,A69.2,10025169,
mondo:0019633,relapsing fever,,13034,,91547,C0035021,,,,D012061,087.9,A68,10038300,
mondo:0019634,familial nasal acilia,,,,922,CN206502,,,,,,,,
mondo:0019635,idiopathic achalasia,"['idiopathic achalasia of esophagus', 'idiopathic achalasia of oesophagus', 'primary achalasia', 'achalasia cardia']",,,930,C1860213,,,,,,,10036669,
mondo:0019636,"renal agenesis, unilateral","['congenital solitary kidney', 'congenital single kidney', 'unilateral renal agenesis']",,,93100,C0266294,,C101220,,,,Q60.0,10053624,
mondo:0019637,renal hypoplasia,"['renal hypoplasia', 'renal hypoplasia (disease)']",0080204,,93101,,,,,,,,10049102,0000089
mondo:0019638,renal dysplasia,"['renal dysplasia (disease)', 'renal dysplasia']",,,93108,,,,,,,,,0000110
mondo:0019639,congenital megacalycosis,,,,93109,,,,,,753.3,,,
mondo:0019640,posterior urethral valve,"['PUV', 'Posterior urethral valves', 'congenital posterior urethral valves']",,,93110,CN227669,,C99021,,,753.8,,10036369,
mondo:0019641,Pauci-immune glomerulonephritis,,,,93126,,,,,,,,,
mondo:0019642,"vitamin D-dependent rickets, type 2","['vitamin D-dependent rickets, type 2', 'HVDRR', 'VDDR2', 'vitamin D receptor deficiency', 'vitamin D-resistant rickets type II', 'hereditary vitamin D-resistant rickets', 'VDRR II', 'VDDR II', 'vitamin D-dependent rickets type II', 'vitamin D dependent rickets 2', 'hypocalcemic vitamin D-resistant rickets', 'hereditary 1,25 dihydroxyvitamin D-resistant rickets with abnormal Vitamin D receptor']",,,93160,,"['0.3896', '0.254', '0.431', '-0.1945', '-0.01407', '-0.1824', '-0.8447', '1.142', '-0.2593', '0.1749', '0.4534', '0.5283', '-0.5483', '0.81', '-0.556', '-0.2825', '-0.1669', '0.0627', '-0.898', '-1.125', '0.04593', '-1.068', '0.874', '-0.4219', '0.472', '-0.2678', '-0.006535', '-0.3518', '0.2415', '-0.2228', '0.3987', '-0.3606', '-0.401', '0.2343', '0.1975', '-0.08575', '-0.1746', '0.2487', '0.703', '0.4915', '-0.2362', '0.03885', '-0.7827', '-0.11926', '0.255', '-0.36', '0.2249', '-0.05603', '-0.0738', '0.2598', '-0.272', '-0.8193', '0.1692', '0.541', '-0.6787', '-0.449', '-0.178', '0.4072', '-1.278', '0.1344', '0.5127', '-0.1311', '-0.3474', '0.564', '0.5615', '0.882', '1.212', '1.169', '-0.669', '-0.556', '0.4043', '-0.1927', '0.738', '-0.5903', '-0.0003424', '1.409', '0.527', '-1.092', '0.4346', '0.3179', '0.1387', '0.1134', '0.4038', '-0.0628', '-0.1825', '0.2036', '0.2627', '0.009705', '0.7197', '0.525', '0.8022', '0.0482', '-0.4546', '0.1643', '-0.646', '0.3467', '0.649', '-0.3784', '-0.3892', '-0.3552']",C131077,,,,E83.3,,
mondo:0019643,transient pseudohypoaldosteronism,['TPHA'],,,93164,CN776908,,,,,,,,
mondo:0019644,"renal dysplasia, unilateral",['unilateral renal dysplasia'],,,93172,,,,,,,,,0008718
mondo:0019645,"renal dysplasia, bilateral",['bilateral renal dysplasia'],,,93173,,,,,,,,,0012582
mondo:0019646,unilateral congenital megacalycosis,,,,93176,,,,,,,,,
mondo:0019647,congenital bilateral megacalycosis,,,,93177,,,,,,,,,
mondo:0019648,achondrogenesis,,0080043,,932,C0001079,"['-0.3772', '0.225', '0.2029', '-0.05276', '0.3948', '-0.544', '-0.007122', '0.19', '-0.51', '0.0662', '-0.2686', '-0.0086', '0.1492', '0.2546', '-0.04367', '0.3254', '0.1964', '0.4102', '0.01257', '-0.4827', '0.1063', '0.4019', '1.162', '0.06183', '0.0724', '0.004936', '0.1456', '-0.2369', '0.1935', '-0.0727', '0.131', '0.0718', '-0.197', '0.5913', '0.1981', '0.0662', '-0.614', '0.2139', '-0.3125', '-0.4292', '0.07025', '-0.757', '-0.2656', '-0.1489', '0.01282', '-0.4634', '0.03198', '0.705', '0.5947', '0.04504', '0.2896', '-0.3323', '-0.0604', '0.09406', '-0.504', '-1.149', '-0.2842', '-0.1145', '-0.1346', '-0.02782', '0.1652', '-0.0268', '0.02022', '0.1761', '-0.2554', '-0.1241', '0.09015', '0.0986', '-0.2389', '0.3245', '-0.00481', '-0.08655', '0.4177', '-0.02267', '-0.01128', '0.3557', '-0.05206', '0.166', '-0.327', '-0.2786', '0.10547', '0.2069', '-0.4087', '-0.08575', '-0.3635', '-0.0674', '0.453', '0.1625', '0.638', '-0.577', '0.04785', '0.08765', '0.1927', '-0.04056', '0.4568', '0.559', '0.36', '-0.3452', '0.3105', '0.0718']",C84527,,C579878,,Q77.0,10066122,
mondo:0019649,idiopathic steroid-sensitive nephrotic syndrome with focal segmental hyalinosis,['idiopathic steroid-sensitive nephrotic syndrome with focal segmental glomerulosclerosis'],,,93206,CN206521,,,,,,,,
mondo:0019650,idiopathic steroid-sensitive nephrotic syndrome with minimal change,['steroid-sensitive MCNS'],,,93207,CN206522,,,,,,,,
mondo:0019651,idiopathic steroid-sensitive nephrotic syndrome with diffuse mesangial proliferation,,,,93209,CN206523,,,,,,,,
mondo:0019652,familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial proliferation,,,,93214,CN206525,,,,,,,,
mondo:0019653,familial idiopathic steroid-resistant nephrotic syndrome with minimal changes,,,,93216,CN206526,,,,,,,,
mondo:0019654,familial idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis,,,,93217,CN206527,,,,,,,,
mondo:0019655,sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis,['sporadic idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis'],,,93218,CN206528,,,,,,,,
mondo:0019656,sporadic idiopathic steroid-resistant nephrotic syndrome with diffuse mesangial sclerosis,,,,93220,CN206529,,,,,,,,
mondo:0019659,Pfeiffer syndrome type 1,['classic Pfeiffer syndrome'],,,93258,CN206533,,,,,,,,
mondo:0019660,Pfeiffer syndrome type 2,,,,93259,CN206534,,,,,,,,
mondo:0019661,Pfeiffer syndrome type 3,,,,93260,CN206535,,,,,,,,
mondo:0019662,"short rib-polydactyly syndrome, Majewski type","['polydactyly with neonatal chondrodystrophy type 2', 'SRPS type 2', 'short rib-polydactyly syndrome type 2', 'short rib-polydactyly syndrome Majewski type']",,,93269,,"['-0.146', '0.2207', '0.3213', '-0.4321', '0.1813', '-0.1613', '-0.0882', '0.188', '-0.4329', '-0.613', '-0.2129', '-0.334', '-0.0691', '0.0467', '-0.6294', '0.05408', '0.1385', '-0.1371', '-0.3406', '-0.3962', '0.1578', '0.0821', '0.4485', '-0.2554', '0.1278', '-0.007164', '-0.2368', '0.2137', '0.7603', '-0.371', '0.4597', '-0.409', '0.42', '0.2688', '0.2534', '-0.11694', '-0.1153', '-0.161', '-0.2568', '-0.2389', '-0.411', '0.0414', '-0.05353', '0.1461', '-0.2438', '-0.5137', '0.0913', '0.5884', '-0.0126', '0.3606', '-0.1232', '0.1874', '-0.124', '0.0448', '-0.5664', '-0.5083', '-0.4243', '0.04184', '-0.0943', '0.1812', '0.374', '-0.02733', '-0.4456', '0.0663', '-0.1368', '-0.1564', '0.1932', '0.1556', '-0.4587', '0.2478', '-0.4956', '0.1425', '0.2793', '0.1583', '-0.1909', '0.0984', '0.0723', '0.196', '-0.2368', '-0.3267', '-0.3623', '-0.07916', '-0.0901', '0.3235', '-0.10736', '0.05103', '-0.1078', '0.1448', '0.01854', '-0.1361', '-0.0967', '-0.12354', '0.07806', '0.1348', '0.8115', '0.1096', '0.3948', '-0.1711', '0.2856', '0.6543']",,,,756.3,,,
mondo:0019665,monostotic fibrous dysplasia,"['monostotic fibrous dysplasia of bone', 'monostotic fibrous dysplasia', 'Jaffe-Lichtenstein disease', 'monostotic fibrous dysplasia (disease)']",,,93277,C0016064,,C53971,,D005358,733.29,Q78.1,,0010736
mondo:0019666,"spondyloepimetaphyseal dysplasia, PAPSS2 type","['spondyloepimetaphyseal dysplasia, Pakistani type', 'spondyloepimetaphyseal dysplasia Pakistani type', 'brachyolmia type 4 with mild epiphyseal and metaphyseal changes', 'BCYM4', 'SEMD, Pakistani type', 'brachyolmia 4 with mild epiphyseal and metaphyseal changes', 'spondylodysplasia and premature pubarche']",0050812,612847,93282,,"['-0.7095', '0.2119', '0.3154', '-0.454', '0.558', '-0.9634', '-0.516', '1.052', '-0.524', '-0.1569', '0.01393', '-0.004585', '0.0766', '-0.1582', '0.01258', '0.3472', '0.566', '-0.02213', '-0.5615', '-0.2092', '-0.05377', '0.0997', '0.6177', '-0.272', '0.12384', '0.2927', '0.05383', '0.2678', '0.4453', '-0.3254', '0.6333', '-0.4924', '-0.079', '0.0325', '0.2123', '-0.3918', '-0.2081', '-0.494', '0.3923', '-0.4805', '-0.0749', '-0.5063', '-0.3406', '0.4436', '-0.3125', '-0.2037', '-0.1373', '0.3977', '0.261', '-0.3235', '0.2915', '0.2024', '-0.1996', '0.09076', '0.1719', '-1.122', '-0.102', '-0.1364', '-0.1986', '0.08484', '0.216', '0.2255', '-0.2832', '0.1276', '-0.3027', '-0.2058', '0.1249', '0.6147', '-0.465', '-0.02798', '-0.7085', '0.02032', '0.2388', '-0.25', '-0.104', '0.4182', '-0.7476', '0.3552', '-0.344', '-0.2996', '-0.2463', '0.2844', '0.2478', '0.2023', '-0.1687', '0.3518', '-0.0761', '0.3438', '0.3035', '-0.1265', '-0.6685', '0.309', '-0.00894', '0.313', '0.491', '0.3376', '0.76', '-0.3806', '0.1531', '0.358']",,,,,,,
mondo:0019667,spondyloepiphyseal dysplasia tarda,,0112284,,93284,,"['-0.45', '0.583', '0.07166', '-0.851', '0.002888', '-0.1838', '0.03857', '0.5854', '-0.6934', '-0.4485', '0.1805', '0.2861', '-0.1917', '0.1694', '0.0653', '-0.11017', '0.3335', '-0.0714', '-0.3582', '-0.535', '-0.4958', '-0.1058', '0.807', '-0.3308', '-0.06757', '-0.11957', '0.1401', '-0.1788', '0.096', '0.1362', '0.3455', '-0.713', '0.02914', '0.2598', '0.3499', '-0.223', '-0.0657', '-0.4226', '0.05212', '-0.01898', '-0.1901', '0.1489', '-0.04495', '0.1738', '0.0966', '0.02148', '-0.2644', '0.2742', '0.2827', '-0.0469', '0.2915', '0.188', '0.0661', '-0.03876', '-0.4207', '-0.4844', '-0.0812', '-0.7505', '0.2281', '-0.0833', '0.4692', '0.1007', '-0.4211', '0.354', '-0.03992', '0.06744', '0.6167', '0.4692', '0.1835', '0.2101', '-0.2233', '0.1274', '0.219', '-0.4177', '-0.102', '0.311', '-0.358', '0.522', '-0.491', '-0.7803', '0.0732', '0.0563', '0.1107', '-0.0749', '-0.213', '0.2942', '-0.04187', '0.1536', '0.0843', '0.2064', '-0.3442', '0.1515', '-0.04498', '0.03647', '0.366', '0.0801', '0.521', '-0.2267', '0.0417', '-0.1277']",,,,756.9,,,
mondo:0019668,adenoma of pancreas,"['adenoma of the pancreas', 'pancreatic adenoma']",,,93292,C4076724,,,,C538110,,D13.6,10058902,
mondo:0019669,hypochondrogenesis,,0080044,,93297,,,,,C563007,,,,
mondo:0019670,ulnar hemimelia,"['congenital longitudinal deficiency of the ulna', 'ulnar longitudinal meromelia', 'ulnar clubhand']",,,93320,,,,,,755.59,,,
mondo:0019671,radial hemimelia,"['congenital longitudinal deficiency of the radius', 'radial clubhand', 'radial longitidinal meromelia', 'radial ray agenesis']",,,93321,,,,,,755.59,,,
mondo:0019672,fibular hemimelia,"['fibular longitudinal meromelia', 'congenital longitudinal deficiency of the fibula']",,,93323,,,,,,,,,
mondo:0019673,postaxial polydactyly type A,"['PAPA', 'postaxial polydactyly type A', 'postaxial polydactyly type A (disease)']",,,93334,C3887487,"['-0.2089', '-0.1396', '0.1991', '0.07184', '0.3252', '-0.3293', '-0.02333', '0.0891', '-0.4717', '-0.4731', '-0.1658', '-0.04834', '-0.001743', '0.1576', '-0.2318', '-0.1985', '0.0986', '-0.2067', '-0.1416', '-0.71', '-0.0903', '0.393', '0.2484', '-0.05246', '0.2146', '0.2372', '-0.1123', '0.1404', '0.1506', '-0.1315', '0.177', '-0.3303', '-0.07904', '0.2612', '0.07623', '-0.0603', '0.2313', '0.0626', '-0.06525', '-0.3147', '-0.09875', '0.02524', '-0.07465', '0.0573', '0.1231', '-0.06323', '-0.1775', '0.3801', '0.10767', '-0.07874', '-0.1603', '-0.193', '0.02327', '-0.06226', '-0.4368', '-0.2878', '0.2258', '-0.02405', '-0.2668', '-0.08826', '0.1344', '0.0585', '-0.2203', '0.1919', '-0.176', '-0.01987', '0.2505', '0.04904', '-0.1857', '0.0642', '-0.268', '0.3337', '0.2957', '-0.266', '0.1603', '0.1554', '-0.013596', '-0.06506', '-0.3296', '-0.3992', '-0.2744', '0.0712', '0.33', '0.505', '0.01029', '-0.102', '-0.3105', '0.2937', '-0.02283', '-0.04578', '-0.1371', '0.2036', '0.196', '0.01477', '0.543', '-0.09485', '0.3052', '-0.555', '0.05585', '0.3308']",,,,,,,0005696
mondo:0019674,postaxial polydactyly type B,['PAPB'],,,93335,C1868120,,,,,,,,
mondo:0019675,spondyloepimetaphyseal dysplasia with joint laxity,"['SEMD-JL', 'spondyloepimetaphyseal dysplasia with joint laxity, Beighton type', 'spondyloepimetaphyseal dysplasia joint laxity', 'spondyloepimetaphyseal dysplasia with joint laxity type 1', 'SEMDJL1', 'SEMDJL', 'spondyloepimetaphyseal dysplasia with joint laxity']",0112197,,93359,,"['-0.25', '0.1498', '0.5366', '-0.522', '0.119', '-0.1523', '0.2583', '0.613', '-0.535', '-0.07684', '-0.1873', '0.02768', '-0.279', '0.185', '-0.09845', '0.1567', '0.2106', '-0.2073', '-0.2008', '-0.263', '0.1195', '0.10425', '0.288', '-0.2095', '-0.2131', '0.06305', '-0.094', '-0.1445', '0.213', '-0.06824', '-0.08777', '-0.1434', '0.261', '0.312', '0.266', '-0.3176', '-0.2239', '-0.318', '0.005013', '-0.547', '0.04675', '-0.38', '-0.0776', '0.2338', '-0.44', '-0.006153', '-0.02493', '0.4978', '0.0221', '0.04733', '-0.1617', '-0.0518', '0.3306', '0.1553', '-0.525', '-0.644', '-0.2064', '-0.1572', '0.0274', '-0.12463', '0.1287', '-0.1041', '-0.62', '0.10156', '-0.3826', '-0.1946', '0.3042', '0.4932', '-0.144', '0.309', '-0.3835', '0.137', '0.1633', '-0.2915', '-0.4211', '0.1526', '0.1752', '0.05908', '-0.2312', '-0.2368', '-0.2306', '-0.172', '0.04343', '0.6343', '-0.2566', '0.05264', '0.12134', '0.532', '0.3252', '0.002531', '-0.0713', '0.4397', '0.03558', '0.4006', '0.6714', '-0.1064', '0.7896', '-0.1769', '0.4768', '0.2935']",,,C562968,756.9,,,
mondo:0019676,brachydactyly type B,,,,93383,C1300267,"['-0.0936', '-0.2512', '0.1757', '0.011826', '0.6587', '-0.2908', '-0.0912', '0.1394', '-0.3572', '-0.5645', '-0.2083', '0.02298', '-0.1021', '0.3489', '-0.1471', '-0.01302', '0.2314', '-0.1365', '0.02867', '-0.5146', '-0.02094', '0.1553', '0.5547', '0.03613', '0.4966', '0.2666', '-0.395', '0.068', '0.12146', '-0.0618', '0.1726', '-0.319', '0.02365', '0.1722', '0.341', '-0.3484', '-0.0965', '-0.3242', '-0.09973', '-0.3684', '-0.0329', '-0.2761', '-0.225', '0.0955', '0.2319', '-0.08203', '-0.1805', '0.631', '0.0892', '-0.1266', '0.10736', '-0.4512', '0.1246', '-0.1404', '-0.9697', '-0.08417', '-0.04648', '-0.2686', '-0.4065', '-0.134', '-0.045', '0.2245', '0.0187', '0.1752', '-0.2478', '-0.1843', '0.03793', '0.2507', '-0.336', '-0.02179', '-0.05362', '0.1422', '0.1313', '-0.474', '0.4514', '0.2068', '-0.012886', '-0.3567', '-0.4592', '-0.752', '-0.307', '-0.0658', '0.4722', '0.3308', '0.06177', '-0.2129', '-0.303', '0.4321', '0.1359', '-0.275', '0.1791', '0.1848', '0.1653', '-0.1317', '0.5244', '-0.11505', '0.191', '-0.8096', '0.388', '0.2216']",,,,,,,
mondo:0019677,brachydactyly type E,['type E brachydactyly'],,,93387,,"['-0.279', '-0.1097', '-0.1821', '-0.06256', '0.3086', '-0.2396', '0.07745', '0.2489', '-0.3557', '-0.2793', '-0.07916', '0.2375', '-0.2386', '0.2285', '-0.1004', '0.01539', '0.285', '-0.2208', '-0.1454', '-0.6396', '0.05212', '0.1979', '0.4622', '0.0667', '0.4575', '0.1744', '-0.0992', '-0.04816', '0.2477', '0.01968', '0.3918', '-0.4458', '-0.1206', '0.1649', '0.3179', '-0.1385', '-0.003138', '-0.4634', '0.0588', '-0.12256', '0.04987', '-0.4326', '-0.07184', '0.1831', '0.03488', '-0.3252', '-0.0894', '0.5664', '0.2399', '-0.043', '0.1503', '-0.287', '-0.1924', '-0.1523', '-0.4583', '-0.3057', '0.03177', '-0.6426', '-0.02948', '-0.0625', '0.006195', '-0.01458', '-0.182', '0.02191', '-0.1809', '-0.1709', '-0.05862', '0.2083', '-0.01483', '0.06836', '-0.3892', '0.1947', '0.1691', '-0.3987', '0.1956', '0.2668', '-0.0376', '-0.2014', '-0.1471', '-0.3545', '-0.10565', '-0.1375', '0.2593', '0.2966', '0.02626', '0.2174', '-0.2632', '0.1879', '0.4578', '0.08923', '0.0838', '0.316', '0.1807', '0.1355', '0.276', '0.004147', '0.319', '-0.6045', '0.3184', '0.3394']",,,,,,,
mondo:0019678,brachydactyly type A5,"['brachydactyly type A5 nail dysplasia', 'absent middle phalanges of digits 2-5 with nail dysplasia', 'brachydactyly with absence of middle phalanges and hypoplastic nails']",,112900,93389,C1862138,,,,C537091,,,,
mondo:0019679,brachydactyly type A7,"['brachydactyly Smorgasbord type', 'brachydactyly, Smorgasbord type']",,,93397,CN206603,,,,,,,,
mondo:0019680,genochondromatosis type 2,,,,93398,CN206604,,,,,,,,
mondo:0019681,juvenile sialidosis type 2,,,,93399,CN206605,,,,,,,,
mondo:0019682,congenital sialidosis type 2,,,,93400,,,,,,,,,
mondo:0019685,FGFR3-related chondrodysplasia,,,,93420,,,,,,,,,
mondo:0019688,sulfation-related bone disorder,"['inborn error of sulphation', 'sulphation disorder']",,,93423,CN227674,,,,,,,,
mondo:0019689,perlecan-related bone disorder,,,,93424,CN227675,,,,,,,,
mondo:0019690,filamin-related bone disorder,['bone filaminopathy'],,,93425,CN227676,,,,,,,,
mondo:0019691,short rib dysplasia,"['short-rib dysplasia (with or without polydactyly)', 'ciliopathies with major skeletal involvement', 'SRP']",,,93426,,"['-0.0635', '0.1141', '0.0881', '-0.0741', '0.09344', '-0.0837', '0.03568', '0.1483', '-0.0828', '-0.0852', '-0.0426', '-0.001572', '-0.02377', '0.01729', '-0.06384', '-0.03165', '0.02661', '-0.04205', '-0.06726', '-0.2172', '0.01146', '0.00747', '0.1436', '-0.04065', '0.03192', '-0.002562', '-0.0139', '-0.03012', '0.02217', '-0.066', '0.0509', '-0.03006', '0.1133', '0.05927', '0.05753', '-0.0666', '0.01373', '-0.09094', '-0.02693', '-0.09143', '0.0139', '-0.09656', '0.0404', '-0.0515', '-0.0254', '-0.06903', '-0.01779', '0.1255', '0.06494', '-0.00472', '-0.004322', '-0.010666', '0.04108', '0.01698', '-0.0728', '-0.09894', '0.0273', '-0.05362', '-0.098', '0.01682', '0.10236', '0.05765', '-0.0842', '0.02211', '-0.014366', '-0.01008', '0.1047', '0.09576', '-0.09784', '0.09546', '-0.0643', '0.0183', '0.04697', '-0.07025', '-0.00941', '0.0595', '-0.002733', '-0.03964', '-0.0578', '-0.0845', '-0.005306', '0.0225', '-0.02942', '0.11383', '-0.04593', '0.04675', '0.03128', '0.11993', '0.10425', '-0.01277', '-0.02591', '0.04797', '0.01429', '0.04404', '0.231', '0.01959', '0.113', '-0.11786', '0.04156', '0.03558']",,,,756.3,,,
mondo:0019692,multiple epiphyseal dysplasia and pseudoachondroplasia,,,,93429,,,,,,,,,
mondo:0019693,multiple metaphyseal dysplasia,,,,93430,,,,,,,,,
mondo:0019694,spondylodysplastic dysplasia,,,,93434,,,,,,,,,
mondo:0019695,acromelic dysplasia,,,,93436,,,,,,,,,
mondo:0019696,acromesomelic dysplasia,['acromesomelic dwarfism'],0080049,,93437,,"['-0.1935', '0.3125', '0.12274', '0.0509', '0.2372', '-0.625', '-0.0276', '0.4138', '-0.4973', '-0.4685', '0.1107', '0.1957', '-0.0981', '0.496', '0.005962', '0.2042', '0.4558', '-0.1592', '-0.04358', '-0.274', '-0.1725', '0.2373', '0.704', '-0.0769', '0.3103', '0.2045', '0.1484', '-0.1726', '0.1191', '-0.003592', '0.2335', '-0.293', '-0.2167', '0.4094', '0.1622', '0.07086', '-0.1203', '-0.2656', '0.06744', '-0.1395', '-0.1137', '-0.2385', '-0.3462', '0.06335', '0.012245', '-0.3376', '0.0809', '0.6616', '0.4587', '-0.1587', '0.244', '-0.1938', '-0.3127', '-0.2231', '-0.1449', '-0.849', '-0.165', '0.1268', '-0.1538', '0.00836', '0.006252', '-0.06415', '-0.3901', '0.1274', '-0.241', '-0.2279', '0.1965', '0.3064', '-0.3286', '0.2449', '0.0829', '-0.09827', '0.4136', '-0.6494', '0.002937', '0.477', '-0.1599', '0.1927', '-0.3079', '-0.3237', '0.0246', '-0.01726', '-0.10284', '0.0978', '-0.07623', '-0.0993', '-0.05878', '0.289', '0.347', '0.423', '-0.3398', '-0.1776', '-0.08734', '-0.0303', '0.343', '0.2793', '0.4756', '-0.139', '0.1718', '0.02756']",,,C535658,,,,
mondo:0019697,mesomelic and rhizo-mesomelic dysplasia,,,,93438,CN229208,,,,,,,,
mondo:0019698,bent bone dysplasia,['campomelic dysplasia and related disorders'],,,93439,C0432238,,,,,756.59,,,
mondo:0019699,slender bone dysplasia,,,,93440,,,,,,,,,
mondo:0019701,chondrodysplasia punctata,"['chondrodysplasia punctata congenita', 'CDP', 'chondrodysplasia punctata (stippled epiphyses) Group', 'chondrodysplasia calcificans congenita']",2581,,93442,C0008445,,C84632,,D002806,756.59,Q77.3,,
mondo:0019702,neonatal osteosclerotic dysplasia,,,,93443,C1300205,,,,,,,,
mondo:0019707,primary osteolysis,,,,93449,,,,,,,,,
mondo:0019712,patellar dysostosis,,,,93455,,,,,,,,,
mondo:0019713,non-syndromic limb reduction defect,"['nonsyndromic limb reduction defect', 'isolated limb reduction defect', 'non-syndromic limb hypoplasia']",,,93457,,,,,,,,,
mondo:0019714,"non-syndromic polydactyly, syndactyly and/or hyperphalangy","['nonsyndromic polydactyly, syndactyly and/or hyperphalangy', 'isolated polydactyly, syndactyly and/or hyperphalangy']",,,93458,,,,,,,,,
mondo:0019716,overgrowth syndrome,,,,93460,CN206621,,C94828,,,,,,
mondo:0019718,lethal chondrodysplasia,,,,93465,,,,,,,,,
mondo:0019719,congenital anomaly of kidney and urinary tract,"['congenital anomalies of the kidney and urinary tract', 'congenital anomalies of kidney and urinary tract', 'renal or urinary tract malformation', 'CAKUT']",0080205,,93545,C1968949,,,,C566906,,,,
mondo:0019720,non-syndromic renal or urinary tract malformation,"['nonsyndromic congenital anomaly of kidney and urinary tract', 'isolated renal or urinary tract malformation', 'nonsyndromic renal or urinary tract malformation']",,,93546,,,,,,,,,
mondo:0019722,glomerular disorder,"['disorder of renal glomerulus', 'glomerulopathies', 'renal glomerulus disease or disorder', 'glomerulopathy', 'renal glomerulus disease', 'disease of renal glomerulus']",,,93548,CN580795,,C120887,,,,N00-N08,,
mondo:0019723,disease of glomerular basement membrane,['basement membrane disease'],,,93550,CN206630,,,,,,,,
mondo:0019724,secondary glomerular disease,,,,93551,CN206631,,,,,,,,
mondo:0019725,pediatric systemic lupus erythematosus,"['SLE, paediatric onset', 'SLE, pediatric onset']",,,93552,,,,,,,,,
mondo:0019726,type II mixed cryoglobulinemia,['MC type II'],,,93554,CN206633,,,,,,D89.1,,
mondo:0019727,mixed cryoglobulinemia type III,['MC type III'],,,93555,CN206634,,,,,,D89.1,,
mondo:0019728,heavy chain deposition disease,['HCDD'],,,93556,CN206635,,C7339,,,,,,
mondo:0019729,light and heavy chain deposition disease,['LHCDD'],,,93557,CN206636,,C158965,,,,,,
mondo:0019730,light chain deposition disease,"['Light-chain deposition disease', 'LCDD', 'Light chain gammopathy', 'Light chain disease', 'Bence Jones myeloma']",,,93558,C0238239,,C7727,,,,,,
mondo:0019731,AApoAI amyloidosis,"['apolipoprotein A-I amyloidosis', 'familial renal amyloidosis due to apolipoprotein A-I variant', 'hereditary amyloid nephropathy due to apolipoprotein A-I variant', 'hereditary renal amyloidosis due to apolipoprotein A-I variant', 'familial amyloid nephropathy due to apolipoprotein A-I variant']",,,93560,CN206638,,,,,,,,
mondo:0019732,ALys amyloidosis,"['hereditary renal amyloidosis due to lysozyme variant', 'familial amyloid nephropathy due to lysozyme variant', 'hereditary amyloid nephropathy due to lysozyme variant', 'familial renal amyloidosis due to lysozyme variant', 'lysozyme amyloidosis']",,,93561,CN206639,,,,,,,,
mondo:0019733,AFib amyloidosis,"['hereditary renal amyloidosis due to fibrinogen A alpha-chain variant', 'fibrinogen A alpha-chain amyloidosis', 'familial amyloid nephropathy due to fibrinogen A alpha-chain variant', 'hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant']",,,93562,CN206640,,,,,,,,
mondo:0019734,juvenile polymyositis,"['JPM', 'juvenile PM']",,,93568,C3826988,,C114358,1001988,,,,,
mondo:0019735,polymyalgia rheumatica,"['rhizomelic pseudopolyarthritis', 'polymyalgia rheumatica']",853,,93569,C1527406,,C85018,,D011111,725,,10068240,
mondo:0019736,dense deposit disease,"['membranoproliferative glomerulonephritis type II', 'glomerulonephritis membranoproliferative type 2', 'Mesangiocapillary glomerulonephritis type 2', 'membranoproliferative glomerulonephritis type 2', 'MPGN 2']",,,93571,C0268743,,C123039,,,,,,
mondo:0019737,thrombotic microangiopathy,,,,93573,C2717961,,C62605,,D057049,446.6,M31.1,10043645,
mondo:0019738,atypical hemolytic-uremic syndrome with H factor anomaly,"['hemolytic-uremic syndrome without diarrhea with H factor anomaly', 'hemolytic-uremic syndrome without diarrhoea with H factor anomaly', 'D-HUS with H factor anomaly', 'aHUS with H factor anomaly', 'atypical HUS with H factor anomaly']",,,93579,CN206650,"['-0.05838', '0.11597', '0.01834', '-0.02591', '0.04565', '-0.07764', '-0.01175', '0.0812', '-0.04703', '-0.01373', '-0.02527', '0.01868', '0.09625', '-0.02864', '-0.1054', '-0.1355', '-0.04446', '-0.05585', '-0.002892', '-0.25', '0.01436', '-0.0855', '0.1583', '-0.0381', '0.11224', '0.05273', '-0.04816', '-0.04263', '0.02403', '-0.075', '0.1516', '0.04276', '0.2233', '0.1099', '-0.004368', '-0.11707', '-0.0697', '-0.06168', '-0.05585', '-0.1624', '0.04797', '-0.1329', '0.05322', '-0.0906', '0.0739', '-0.1431', '-0.0825', '0.11414', '-0.00951', '0.0387', '-0.03366', '-0.04416', '-0.02634', '-0.003582', '-0.1326', '-0.04745', '0.10333', '-0.11847', '-0.2047', '0.07227', '0.1094', '0.02328', '0.04102', '0.001503', '0.06476', '0.02707', '0.1694', '0.0323', '-0.1797', '0.1975', '-0.1594', '-0.02248', '0.04468', '-0.07764', '0.0931', '-0.03094', '0.010895', '-0.01666', '-0.07434', '-0.05472', '-0.005417', '0.02937', '-0.04605', '0.0964', '-0.0748', '-0.06354', '0.0589', '0.148', '0.11316', '-0.04272', '0.1582', '0.1326', '0.01487', '0.009995', '0.2625', '0.0903', '0.1042', '-0.2328', '-0.04846', '0.07654']",,,,,,,
mondo:0019739,atypical hemolytic-uremic syndrome with anti-factor H antibodies,"['hemolytic-uremic syndrome without diarrhea with anti-factor H antibodies', 'aHUS with anti-factor H antibodies', 'D-HUS with anti-factor H antibodies', 'hemolytic-uremic syndrome without diarrhoea with anti-factor H antibodies', 'atypical HUS with anti-factor H antibodies']",,,93581,CN206652,"['-0.0729', '0.1626', '-0.00686', '-0.011215', '0.009605', '-0.1216', '-0.0001199', '0.05197', '-0.04428', '-0.04715', '-0.01865', '-0.0001878', '0.05756', '0.003323', '-0.03848', '-0.0821', '-0.05902', '-0.05005', '0.00955', '-0.2166', '-0.008', '-0.0395', '0.1371', '-0.02278', '0.07904', '-0.01528', '-0.0234', '-0.08746', '0.00653', '-0.08374', '0.1116', '0.0432', '0.1609', '0.05096', '0.038', '-0.08185', '-0.008064', '-0.01447', '-0.04446', '-0.1519', '0.03525', '-0.1278', '0.06198', '-0.1034', '0.00654', '-0.1307', '-0.0658', '0.04977', '0.01361', '0.07526', '-0.01764', '-0.03256', '-0.02661', '0.04028', '-0.145', '-0.001614', '0.1355', '-0.08386', '-0.1688', '0.0847', '0.0963', '0.04648', '-0.006298', '0.01703', '0.004047', '-0.0227', '0.1792', '0.0768', '-0.1321', '0.2059', '-0.08136', '-0.01971', '0.0373', '-0.1342', '0.0627', '0.03772', '-0.00727', '0.008286', '-0.07574', '-0.0806', '-0.03574', '0.02498', '-0.02248', '0.0544', '-0.0926', '-0.04803', '0.06323', '0.11584', '0.1088', '-0.004017', '0.1575', '0.0822', '-0.01054', '0.02611', '0.2223', '0.0872', '0.10913', '-0.2124', '-0.05508', '0.05173']",,,,,,,
mondo:0019740,acquired thrombotic thrombocytopenic purpura,"['purpura, thrombotic thrombocytopenic', 'Moschowitz syndrome', 'TTP', 'acquired TTP', 'idiopathic thrombotic thrombocytopenic purpura', 'autoimmune thrombotic thrombocytopenic purpura', 'acquired thrombotic thrombocytopenic purpura', 'acquired ADAMTS13 deficiency']",,,93585,C2584778,,C131653,,C536901,,M31.3,,
mondo:0019741,familial cystic renal disease,['hereditary cystic kidney disease'],,,93587,CN206655,,,,,,,,
mondo:0019742,late-onset nephronophthisis,,,,93589,,"['-0.04288', '0.04752', '-0.03757', '-0.003702', '0.05505', '-0.1099', '0.00995', '0.08606', '-0.0669', '-0.04123', '-0.0418', '-0.03073', '-0.02596', '0.01008', '0.01245', '-0.0899', '-0.05283', '-0.03503', '-0.01432', '-0.1576', '-0.004826', '-0.014305', '0.04315', '-0.01653', '0.05777', '-0.02385', '-0.0154', '-0.02797', '-0.0002768', '-0.05612', '0.06866', '0.0348', '0.0317', '0.04083', '0.015564', '-0.0284', '-0.02135', '-0.05173', '0.01077', '-0.01573', '0.03885', '-0.05582', '0.0554', '0.08344', '0.002993', '-0.03162', '-0.01773', '0.01968', '0.005054', '0.00271', '0.01942', '-0.001207', '-0.007767', '-0.02347', '-0.01474', '-0.06744', '0.1167', '-0.0859', '-0.1044', '0.04694', '0.08997', '0.0325', '0.0367', '0.04047', '0.0002325', '-0.02643', '0.104', '0.0666', '-0.067', '0.0785', '-0.05484', '0.002008', '0.04996', '-0.02383', '0.03857', '-0.00489', '0.01888', '-0.007442', '-0.02838', '-0.000764', '-0.00998', '-0.02562', '-0.01513', '0.0636', '-0.04584', '0.002653', '0.05637', '0.04837', '0.06113', '-0.008675', '0.05606', '0.09045', '0.01187', '0.002895', '0.1786', '0.02617', '0.1163', '-0.09766', '-0.01248', '0.03702']",,,,,,,
mondo:0019743,nephropathy secondary to a storage or other metabolic disease,,,,93593,CN206659,,,,,,,,
mondo:0019745,cystinuria type A,,,,93612,,"['-0.03235', '0.0644', '0.0453', '0.00819', '0.04108', '-0.1118', '-0.000231', '0.0982', '-0.08765', '-0.01788', '-0.03763', '0.006954', '0.0002534', '0.02104', '-0.05933', '-0.0334', '0.00604', '-0.02539', '-0.0119', '-0.1436', '-0.02374', '-0.02846', '0.0812', '-0.01837', '0.007744', '-0.01712', '-0.03345', '-0.0134', '-0.0001338', '-0.03064', '0.0826', '0.01514', '0.096', '0.03867', '-0.02211', '-0.05286', '-0.0102', '-0.03546', '-0.02798', '-0.0664', '-0.0067', '-0.06433', '0.02913', '-0.004524', '-0.03418', '-0.0502', '-0.01654', '0.05563', '-0.01823', '0.0187', '-0.005726', '-0.01466', '-0.00953', '-0.03592', '-0.04724', '-0.03885', '0.0422', '-0.03098', '-0.0861', '0.009224', '0.03366', '0.033', '0.01532', '-0.01162', '0.02309', '-0.00433', '0.0761', '0.0265', '-0.09686', '0.0559', '-0.05643', '0.03098', '0.01723', '-0.0662', '0.05713', '0.0443', '-0.01421', '0.01582', '-0.04712', '-0.003534', '-0.005417', '-0.01083', '-0.0394', '0.03174', '-0.00482', '0.02129', '0.02791', '0.0707', '0.0961', '0.01215', '0.02568', '0.0823', '-0.00979', '0.0007725', '0.1353', '0.04202', '0.0649', '-0.11145', '-0.006287', '0.0337']",,,C565652,,,,
mondo:0019746,cystinuria type B,,,,93613,C1857389,"['-0.006752', '0.1261', '0.05942', '-0.008415', '0.06506', '-0.1477', '-0.01322', '0.0721', '-0.0832', '-0.03723', '-0.05188', '-0.01334', '0.006256', '0.01674', '-0.0658', '-0.0497', '0.0008807', '-0.013855', '-0.02371', '-0.1565', '-0.00729', '-0.0597', '0.1298', '-0.012825', '0.04874', '-0.03156', '-0.02092', '-0.0502', '-0.02676', '-0.0822', '0.1003', '0.04602', '0.11487', '0.02876', '0.01455', '-0.0665', '-0.04745', '-0.05984', '-0.04733', '-0.1151', '0.0031', '-0.0984', '0.006096', '-0.03014', '-0.05832', '-0.12317', '-0.01233', '0.05432', '0.000709', '0.02315', '0.0201', '-0.05548', '-0.004566', '-0.02881', '-0.09576', '-0.02272', '0.063', '-0.05615', '-0.1271', '0.02336', '0.009094', '0.02928', '0.03793', '0.00975', '0.04147', '0.02374', '0.1065', '0.02432', '-0.1097', '0.09344', '-0.09436', '0.001203', '0.01852', '-0.0852', '0.08716', '0.05316', '-0.0339', '-0.0188', '-0.07465', '0.00807', '0.004402', '-0.003017', '-0.0757', '0.03043', '-0.03336', '0.01927', '0.07196', '0.07983', '0.1493', '0.01526', '0.0655', '0.1028', '0.0002191', '-0.02576', '0.1566', '0.0956', '0.06323', '-0.1874', '-0.00856', '0.00837']",,,,,,,
mondo:0019751,autoinflammatory syndrome,,,,93665,C3890737,,C119050,,,,M04-M04,10072220,
mondo:0019752,pediatric Castleman disease,,,,93682,CN206684,,,,,,,,
mondo:0019753,localized Castleman disease,"['localised Angiofollicular lymphoid hyperplasia', 'localized Angiofollicular lymphoid hyperplasia', 'Unicentric angiofollicular lymph hyperplasia', 'Unicentric Castleman disease', 'Unicentric angiofollicular ganglionic hyperplasia', 'localized Castleman disease']",,,93685,CN206685,,C115200,,,,,,
mondo:0019754,multicentric Castleman disease,"['Human herpesvirus-8-associated multicentric Castleman disease', 'idiopathic multicentric Castleman^s disease', 'HHV-8-associated multicentric Castleman disease', 'multicentric Castleman^s disease', 'multicentric plasma cell variant of Castleman^s disease', 'MCD', 'PMCD', 'multicentric giant lymph node hyperplasia', 'plasmablastic multicentric Castleman disease', 'multicentric Angiofollicular lymphoid hyperplasia']",0111152,,93686,C1334815,,C27855,,,,,,
mondo:0019755,developmental defect during embryogenesis,"['rare developmental defect during embryogenesis', 'disorder of embryonic morphogenesis', 'embryonic morphogenesis disease', 'malformation syndrome']",,,93890,CN206687,,C99267,,,759.7,,,
mondo:0019756,lobar holoprosencephaly,,,,93924,,,,,,,,,
mondo:0019757,alobar holoprosencephaly,,,,93925,,,,,,,,,
mondo:0019758,midline interhemispheric variant of holoprosencephaly,"['MIH type HPE', 'middle interhemispheric variant of holoprosencephaly', 'MIHF', 'MIHV', 'MIH', 'Syntelencephaly', 'middle interhemispheric fusion variant']",,,93926,CN206692,,,,,,,,
mondo:0019759,epispadias,"['epispadias (disease)', 'epispadias']",,,93928,CN227686,,C98923,,D004842,752.62,,10015088,0000039
mondo:0019760,terminal transverse defects of arm,['congenital limb amputation'],,,93937,C1857578,,,,C565681,,,,
mondo:0019761,laryngotracheoesophageal cleft type 1,"['laryngo-tracheo-esophageal cleft type 1', 'LTEC1', 'LTEC I']",,,93938,CN206696,,,,,,,,
mondo:0019762,laryngotracheoesophageal cleft type 2,"['LTEC2', 'laryngo-tracheo-esophageal cleft type 2', 'LTEC II']",,,93939,CN206697,,,,,,,,
mondo:0019763,laryngotracheoesophageal cleft type 3,"['LTEC3', 'LTEC III', 'laryngo-tracheo-esophageal cleft type 3']",,,93940,CN206698,,,,,,,,
mondo:0019764,laryngotracheoesophageal cleft type 4,"['LTEC4', 'laryngo-tracheo-esophageal cleft type 4', 'LTEC IV']",,,93941,CN206699,,,,,,,,
mondo:0019766,"X-linked intellectual disability, Porteous type",,,,93945,CN206701,,,,,,,,
mondo:0019767,hamel cerebro-palato-cardiac syndrome,,,,93946,CN206702,,,,,,,,
mondo:0019768,"X-linked intellectual disability, Golabi-Ito-hall type",,,,93947,CN206703,,,,,,,,
mondo:0019769,"X-linked intellectual disability, Sutherland-Haan type",,,,93950,CN206704,,,,,,,,
mondo:0019770,X-linked dominant intellectual disability-epilepsy syndrome,,,,93951,CN227687,"['1.041', '0.1904', '-0.3208', '-0.0798', '-0.3398', '-0.3445', '0.7754', '0.2239', '-0.5337', '-0.4153', '0.217', '-0.235', '-0.565', '0.353', '-0.01205', '-0.0695', '-0.347', '-0.3684', '-0.6646', '-0.8013', '-0.2343', '0.8276', '0.09845', '-0.5386', '-0.1726', '-0.06964', '0.006954', '-0.05798', '-0.3044', '0.4011', '0.1909', '-0.726', '0.341', '0.117', '0.754', '0.4226', '0.0009537', '0.124', '-0.1548', '-0.4978', '-0.32', '-0.475', '0.0711', '-0.2057', '-0.626', '-0.834', '-0.1837', '0.313', '0.56', '0.532', '-0.2043', '0.1469', '0.05173', '-0.2903', '0.04282', '-0.0449', '-0.07715', '0.1289', '-0.1152', '0.3083', '-1.014', '0.7275', '0.6294', '-0.2495', '-0.3228', '1.416', '0.2284', '0.05508', '-1.078', '0.621', '1.043', '1.018', '0.01805', '-0.469', '0.216', '0.837', '0.87', '0.535', '-0.4258', '0.3525', '-0.2491', '0.8115', '0.305', '0.273', '0.3513', '0.3079', '0.2018', '0.549', '0.7935', '0.3481', '-0.0372', '-0.05673', '-0.176', '0.1415', '0.12146', '0.2698', '0.2646', '-0.685', '0.3005', '0.291']",,,,,,,
mondo:0019771,oromandibular dystonia,,0050843,,93958,C0393607,,,,,,,,
mondo:0019772,blepharospasm-oromandibular dystonia syndrome,"['Meige syndrome', 'blepharospasm-oromandibular dystonia', 'Meige dystonia', 'Meige^s syndrome', 'oral facial dystonia', 'segmental cranial dystonia', 'Brueghel syndrome', 'blepharospasm - oromandibular dystonia', 'idiopathic blepharospasm-oromandibular dystonia syndrome']",3982,,93964,,,,,D008538,,,,
mondo:0019773,myelomeningocele,['meningomyelocele'],0060326,,93969,,,,1001369,D008591,,,,0002475
mondo:0019780,anotia,,,,93976,,,,,,744.01,,10002654,
mondo:0019781,astrocytoma (excluding glioblastoma),['astrocytoma'],,,,C0004114,,C60781,,D001254,,,,
mondo:0019782,humero-ulnar synostosis,['humero-ulnar fusion'],,,94056,,,,,,,,,
mondo:0019783,neovascular glaucoma,['secondary angle-closure glaucoma with rubeosis'],1687,,94058,C0017609,,,1001060,D015355,,,10062891,
mondo:0019784,12q14 microdeletion syndrome,"['osteopoikilosis-short stature-intellectual disability syndrome', 'deletion 12q14', 'monosomy 12q14', 'Del(12)(q14)']",,,94063,CN206727,,,,,,,,
mondo:0019786,severe intellectual disability-epilepsy-anal anomalies-distal phalangeal hypoplasia,,,,94066,,,,,,,,,
mondo:0019787,autoimmune enteropathy,"['immune-mediated protracted diarrhea of infancy', 'immune-mediated protracted diarrhoea of infancy', 'severe immune-mediated enteropathy']",,,94075,C0341305,,C94694,,C538273,279.49,,,
mondo:0019788,non-secreting paraganglioma,['non-functioning paraganglioma'],,,94080,,,,,,,,,
mondo:0019789,cytophagic histiocytic panniculitis,"['Winkelmann cytophagic panniculitis', 'CHP']",,,94087,C0406594,,,,,,,,
mondo:0019790,neuroleptic malignant syndrome,['NMS'],14464,,94093,C0027849,,C94829,1001379,D009459,333.92,G21.0,10029282,
mondo:0019791,recessive mitochondrial ataxia syndrome,['MIRAS'],,,94125,CN206743,,,0008816,,,,,
mondo:0019792,autosomal dominant cerebellar ataxia type I,"['autosomal dominant cerebellar ataxia type 1', 'cerebellar plus syndrome', 'ADCAI', 'ADCA1']",,,94145,CN206744,"['0.0327', '-0.07983', '-0.2021', '0.1395', '-0.3071', '-0.901', '0.471', '0.1432', '-0.736', '-0.9326', '0.001011', '0.1439', '-0.1403', '0.0671', '0.8594', '-0.158', '-0.06995', '-0.5254', '0.139', '-0.6616', '-0.1122', '-0.5205', '0.2952', '-0.558', '0.2312', '-0.5557', '-0.432', '0.1296', '-0.2324', '-1.006', '0.1498', '0.3372', '-0.6294', '-0.2769', '0.406', '0.00688', '-0.000479', '0.1572', '0.4714', '0.6167', '0.357', '0.1963', '-0.3716', '0.2913', '0.6313', '-0.5723', '0.2043', '0.2324', '0.537', '-0.05545', '-0.1649', '0.1399', '-0.12384', '-0.61', '0.02292', '-0.549', '0.4128', '0.49', '-0.1483', '0.3264', '-0.536', '0.2084', '0.2637', '-0.2688', '-0.4224', '0.5166', '0.3335', '0.3523', '-0.522', '0.3525', '0.522', '0.3616', '-0.1197', '-0.607', '0.6885', '0.2485', '0.3193', '-0.2576', '-0.003565', '0.2957', '-0.0642', '-0.951', '0.3335', '0.663', '-0.2192', '-0.711', '0.2063', '0.06287', '0.4673', '0.3738', '0.4434', '0.497', '0.00952', '-0.2191', '1.07', '0.9155', '0.5654', '0.5635', '-0.1859', '-0.0315']",,,,,,,
mondo:0019793,autosomal dominant cerebellar ataxia type III,"['Pure cerebellar syndrome-mild pyramidal signs syndrome', 'autosomal dominant cerebellar ataxia type III', 'ADCAIII', 'autosomal dominant cerebellar ataxia type 3', 'ADCA3']",,,94148,CN206746,,,,,,,,
mondo:0019794,autosomal dominant cerebellar ataxia type IV,"['ADCA4', 'autosomal dominant cerebellar ataxia type IV', 'ADCAIV', 'autosomal dominant cerebellar ataxia type 4']",,,94149,CN229225,,,,,,,,
mondo:0019795,acalvaria,"['Acrania', 'primary acalvaria']",,,945,C2930936,,,,D009436,,,,
mondo:0019796,acrocephalosyndactyly,"['ACS', 'acrocephalosyndactylia', 'acrocephalosyndactyly']",12960,,946,,"['0.163', '-0.265', '0.02647', '0.099', '0.11957', '-0.4688', '0.4678', '0.3813', '-0.2047', '-0.4534', '0.1704', '-0.363', '-0.271', '0.1792', '-0.05542', '0.1704', '0.1044', '-0.4802', '-0.2057', '-1.07', '-0.2041', '0.709', '1.025', '-0.05255', '0.4373', '0.1978', '-0.4006', '-0.0457', '0.375', '-0.09344', '0.4993', '-0.34', '0.3274', '0.7036', '0.183', '-0.2766', '-0.2069', '-0.1328', '-0.5415', '-0.381', '-0.10443', '-0.4033', '0.1021', '-0.4414', '0.6816', '-0.4119', '0.12384', '0.4758', '0.3079', '-0.006203', '-0.02263', '-0.222', '-0.2352', '-0.2915', '-0.4824', '-0.2896', '-0.04865', '-0.02039', '-0.1809', '-0.09265', '-0.02443', '-0.4878', '0.4019', '0.4402', '-0.156', '0.3767', '-0.06335', '0.1099', '-0.3828', '0.591', '-0.754', '0.3408', '0.27', '-0.1421', '0.3345', '0.6177', '0.07855', '-0.3516', '-0.7', '-0.564', '-0.0821', '0.005928', '-0.1912', '0.2874', '0.3225', '-0.3225', '-0.1696', '0.08844', '-0.1631', '-0.337', '-0.113', '0.1346', '0.2434', '-0.08765', '-0.2937', '0.246', '0.6147', '-0.422', '0.4229', '0.299']",C34348,0004123,,755.55,,10000590,
mondo:0019797,acrodysostosis,"['nasal hypoplasia-peripheral dysostosis-intellectual disability syndrome', 'Arkless-Graham syndrome', 'peripheral dysostosis-nasal hypoplasia-intellectual disability (PNM) syndrome', 'Maroteaux-Malamut syndrome', 'acrodysplasia']",14669,,950,C0220659,"['-0.0674', '-0.01052', '0.533', '-0.2058', '0.0976', '0.2119', '0.1567', '0.6997', '-0.5317', '-1.193', '-0.0842', '-0.2922', '-0.01889', '0.1359', '0.1648', '0.3875', '0.2385', '-0.04578', '-0.552', '-0.5044', '0.34', '-0.1284', '0.5635', '-0.149', '0.0233', '0.3862', '-0.34', '-0.4277', '0.4382', '-0.2695', '0.03622', '-0.475', '0.04248', '0.363', '0.1869', '0.04868', '-0.223', '-0.1332', '-0.2979', '-0.3552', '0.385', '-0.1672', '0.6274', '0.03787', '0.722', '-0.534', '0.355', '0.3706', '-0.2302', '-0.2537', '-0.2152', '0.545', '-0.02573', '0.1362', '-0.3792', '-0.2588', '-0.11163', '-0.8394', '0.06964', '0.5806', '0.005165', '0.2617', '-0.3042', '-0.01151', '-0.05536', '0.4446', '-0.2007', '0.821', '-0.08356', '-0.1963', '-0.563', '0.05872', '0.01187', '-0.07544', '0.7817', '0.308', '-0.257', '-0.7124', '-0.8394', '-0.0484', '-0.1466', '0.1691', '-0.653', '-0.012535', '-0.1625', '0.4941', '0.556', '0.065', '0.823', '0.0586', '0.4841', '-0.001435', '-0.3264', '-0.1383', '0.6235', '-0.3093', '0.014206', '-0.6987', '0.3184', '0.1877']",,,C538179,756.59,,,
mondo:0019799,hepatoerythropoietic porphyria,['HEP'],5230,,95159,C0162569,,C84754,,D017121,,,,
mondo:0019800,chronic hepatic porphyria,"['chronic acute hepatic porphyria', 'acute hepatic porphyria, chronic']",,,95161,,,,,,,,,
mondo:0019801,acute adrenal insufficiency,"['acute adrenal failure', 'adrenocortical crisis', 'Addisonian crisis', 'adrenal crisis', 'acute adrenocortical insufficiency']",,,95409,C0151467,,C112840,,,255.41,,,
mondo:0019802,secondary short bowel syndrome,,,,95427,CN206757,,,,,,,,
mondo:0019803,angioma serpiginosum,['angioma serpiginosum of skin'],4028,,95429,CN206759,,C3926,,,,,,
mondo:0019804,tracheomalacia,"['congenital tracheomalacia', 'type 1 tracheomalacia', 'tracheomalacia, congenital', 'congenital major airway collapse']",0060313,,95430,C0948187,,C98634,,D055090,748.3,,10010654,0002779
mondo:0019805,twin to twin transfusion syndrome,"['foetal transfusion syndrome', 'Twin to twin transfusion', 'Twin-to-twin blood transfer', 'Twin-Twin transfusion syndrome', 'foetal haemorrhage into co-twin', 'Feto-fetal transfusion syndrome', 'placental transfusion syndrome', 'TTTS', 'foetal blood loss from foetal haemorrhage into co-twin', 'fetal hemorrhage into co-twin', 'twin-to-twin transfusion syndrome', 'fetal blood loss from fetal hemorrhage into co-twin', 'fetal transfusion syndrome', 'Fetofetal transfusion syndrome', 'stuck Twin syndrome']",13576,,95431,CN206761,,C113824,1001221,D005330,,,10058328,
mondo:0019806,primary progressive aphasia,"['primary progressive aphasia syndrome', 'PPA', 'Mesulam syndrome']",,,95432,C0282513,,C85024,0009053,D018888,,,,
mondo:0019807,mesocardia,"['mesocardia', 'mesocardia (disease)', 'Midline heart']",,,95443,,,,,,746.87,,,0011599
mondo:0019808,aortic valve atresia,"['congenital aortic valve atresia', 'congenital atresia of aortic valve', 'aortic valve atresia (disease)', 'aortic valve atresia']",,,95448,,,C98818,,,,,10066801,0010883
mondo:0019809,congenital aortic valve insufficiency,"['Congential aortic valve insufficiency', 'congenital insufficiency of aortic valve', 'congenital aortic insufficiency']",,,95449,C0158617,,C103936,,,746.4,,10010370,
mondo:0019810,toxic epidermal necrolysis,"['Lyell^s syndrome', 'Lyell syndrome', 'SJS-TEN', 'Stevens-Johnson syndrome/toxic epidermal necrolysis spectrum', 'TEN', 'toxic epidermolysis']",,,95455,C0014518,,C79777,0004775,,695.15,,10044223,
mondo:0019811,tricuspid valve agenesis,['congenital unguarded tricuspid orifice'],,,95457,,,,,,,Q22.4,,
mondo:0019813,congenital tricuspid stenosis,,,,95459,,,,,,,Q22.4,10010656,
mondo:0019814,straddling or overriding tricuspid valve,,,,95461,,,,,,,,,
mondo:0019815,accessory tricuspid valve tissue,,,,95462,,,,,,,,,
mondo:0019816,anomaly of the tricuspid subvalvular apparatus,,,,95463,,,,,,,,,
mondo:0019817,congenital mitral valve insufficiency and/or stenosis,,,,95464,,,,,,,Q23,,
mondo:0019818,cleft mitral valve,,,,95465,,,,,,,,,
mondo:0019819,double-orifice mitral valve,,,,95474,,,,,,746.89,,,
mondo:0019820,univentricular cardiopathy,,,,95483,,,,,,,,,
mondo:0019821,aneurysm or dilatation of ascending aorta,,,,95484,,,,,,,,,
mondo:0019822,arterial duct anomaly,['patent ductus arteriosus anomalies'],,,95485,,,,,,,,,
mondo:0019823,premature closure of the arterial duct,['premature closure of the patent ductus arteriosus'],,,95486,,,,,,,,,
mondo:0019824,non-acquired pituitary hormone deficiency,,,,95488,,,,,,,E23.0,,
mondo:0019825,congenital coronary artery aneurysm,['congenital coronary aneurysm'],,,95491,,,,,,,,,
mondo:0019826,abnormal origin or aberrant course of coronary artery,,,,95493,,,,,,,,,
mondo:0019828,pituitary stalk interruption syndrome,"['ectopic neurohypophysis', 'hypoplastic anterior pituitary, missing stalk, and ectopic posterior pituitary', 'PSIS']",,,95496,CN206776,,C121150,,,,,,
mondo:0019829,congenital anomaly of superior vena cava,"['congenital anomaly of superior caval vein', 'congenital anomaly of the SVC']",,,95498,,,,,,747.49,,,
mondo:0019830,congenital anomaly of the inferior vena cava,"['congenital anomaly of the IVC', 'congenital anomaly of the inferior caval vein']",,,95499,,,,,,747.49,,,
mondo:0019831,congenital anomaly of the coronary sinus,,,,95500,,,,,,,,,
mondo:0019832,acquired pituitary hormone deficiency,['acquired hypopituitarism'],,,95502,,,,,,,E23.0,,
mondo:0019835,primary hypophysitis,"['autoimmune hypophysitis', 'lymphocytic hypophysitis']",,,95506,,,C132055,,D000069281,279.49,,,
mondo:0019836,congenital anomaly of hepatic vein,,,,95507,,,,,,,,,
mondo:0019837,atrial appendage anomaly,['atrial auricle anomaly'],,,95510,,,,,,,,,
mondo:0019838,adenohypophysitis,"['adenohypophysis inflammation', 'lymphocytic adenohypophysitis', 'anterior pituitary hypophysitis']",,,95512,,,,,,,,,
mondo:0019839,panhypophysitis,['Infundibulo-panhypophysitis'],,,95513,,,,,,,,,
mondo:0019840,acropectororenal dysplasia,"['acro-pectoro-renal field defect', 'brachydactyly, absent pectoral muscles and agenesis/hypoplasia of kidneys']",,,956,,,,,,,,,
mondo:0019844,pituitary hormone deficiency secondary to storage disease,,,,95618,CN206788,,,,,,,,
mondo:0019845,iatrogenic or traumatic pituitary deficiency,,,,95619,,,,,,,,,
mondo:0019846,acquired central diabetes insipidus,"['acquired neurogenic diabetes insipidus', 'acquired CDI', 'acquired central diabetes insipidus']",,,95626,,,,,,,E23.2,,
mondo:0019848,posterior hypospadias,"['perineal, scrotal or penoscrotal hypospadias']",,,95706,,,,,,,,,
mondo:0019849,isolated micropenis,,,,95707,,,,,,,,,
mondo:0019851,acquired primary ovarian failure,"['acquired premature ovarian failure', 'acquired primary ovarian failure']",,,95709,C4303540,,,,,,,,
mondo:0019852,inherited primary ovarian failure,"['inherited premature ovarian failure', 'hereditary primary ovarian failure']",,,95710,,"['-0.168', '0.07074', '-0.00786', '0.1465', '0.1149', '-0.2388', '0.0659', '-0.0114', '-0.06216', '-0.1616', '0.1814', '0.0685', '-0.01311', '-0.005196', '-0.2048', '-0.421', '0.06964', '0.03064', '-0.1021', '-0.4976', '-0.1085', '-0.1821', '0.1459', '-0.3943', '0.2395', '0.0359', '0.2279', '0.10034', '0.07245', '-0.1221', '0.4153', '0.1907', '0.1896', '-0.165', '-0.1356', '-0.10126', '0.04895', '0.0809', '0.06168', '-0.1338', '0.2059', '0.1096', '0.13', '-0.1255', '-0.0696', '-0.1093', '-0.0489', '-0.3013', '0.287', '0.2563', '0.01529', '-0.1436', '-0.123', '0.2114', '-0.2915', '-0.1761', '0.14', '-0.01106', '-0.4004', '0.09125', '0.3357', '0.1462', '0.1807', '0.07056', '-0.01477', '0.04095', '0.346', '0.2443', '-0.3516', '0.0681', '-0.285', '0.1121', '0.244', '-0.1675', '0.00612', '0.1594', '0.218', '0.09436', '-0.2153', '-0.22', '-0.1076', '0.2283', '-0.1458', '-0.03638', '-0.1236', '-0.1143', '0.271', '-0.0702', '0.11304', '-0.02522', '-0.1328', '0.3384', '-0.08105', '0.06232', '0.282', '0.1316', '0.2932', '-0.17', '-0.04614', '0.05884']",,,,,E28.3,,
mondo:0019854,thyroid ectopia,,,,95712,,,,,,,,,
mondo:0019855,athyreosis,,,,95713,,,,,,,,,
mondo:0019857,congenital hypothyroidism due to transplacental passage of maternal TSH-binding inhibitory antibodies,,,,95715,C4273914,,,,,,,,
mondo:0019858,idiopathic congenital hypothyroidism,,,,95717,C4273913,,,,,,,,
mondo:0019860,thyroid hemiagenesis,,,,95719,C4023190,,,,,,,,
mondo:0019861,thyroid hypoplasia,,,,95720,,,,,,,,10065938,
mondo:0019862,levocardia,"['levocardia-situs inversus', 'Isolated levocardia with situs inversus', 'Situs inversus with levocardia']",,,95854,C0023569,,C111647,,D007979,,Q24.1,10071015,
mondo:0019864,tetrasomy 21,"['Isochromosome 21', 'tetrasomy type 21']",,,96055,,,,,,,,,
mondo:0019865,mosaic trisomy 4,"['trisomy 4 mosaicism', 'Mosaic trisomy type 4', 'Mosaic trisomy chromosome 4']",,,96059,,,,,,,,,
mondo:0019866,mosaic trisomy 5,"['trisomy 5 mosaicism', 'Mosaic trisomy type 5', 'Mosaic trisomy chromosome 5']",,,96060,,,,,C537762,,,,
mondo:0019867,mosaic trisomy 8,"['trisomy 8 mosaicism', 'Mosaic trisomy type 8', 'Warkany syndrome', 'Mosaic trisomy chromosome 8']",,,96061,,,,,C537940,,,10053916,
mondo:0019868,mosaic trisomy 10,"['trisomy 10 mosaicism', 'uniparental disomy of 10', 'Mosaic trisomy type 10', 'Mosaic trisomy chromosome 10', 'chromosome 10, uniparental disomy', 'mosaic trisomy 10']",,,96063,CN035866,,,,C538292,,,,
mondo:0019869,mosaic trisomy 22,"['Mosaic trisomy chromosome 22', 'Mosaic trisomy type 22', 'trisomy 22 mosaicism']",,,96068,,,,,C536796,,,,
mondo:0019870,distal trisomy 1p36,"['trisomy 1pter', 'distal trisomy type 1p36', 'distal duplication 1p36', 'telomeric duplication 1p36']",,,96069,CN244049,,,,,,,,
mondo:0019871,distal trisomy 2p,"['trisomy 2pter', 'telomeric duplication 2p', 'distal trisomy type 2p', 'distal duplication 2p']",,,96070,,,,,,,,,
mondo:0019872,distal trisomy 3p,"['telomeric duplication 3p', 'distal duplication 3p', 'trisomy 3pter', 'distal trisomy type 3p']",,,96071,,,,,,,,,
mondo:0019873,4p16.3 microduplication syndrome,"['telomeric duplication 4p', 'distal trisomy 4p', 'distal duplication 4p', 'trisomy 4pter']",,,96072,CN206808,,,,,,,,
mondo:0019874,distal trisomy 7p,"['trisomy 7pter', 'distal trisomy type 7p', 'distal duplication 7p', 'telomeric duplication 7p']",,,96074,,,,,,,,,
mondo:0019875,Beckwith-Wiedemann syndrome due to 11p15 microduplication,,,,96076,CN206810,,,,,,,,
mondo:0019876,8p inverted duplication/deletion syndrome,"['inverted 8p duplication/deletion syndrome', 'Invdupdel(8p)']",,,96092,CN206812,,,,,,,,
mondo:0019877,distal trisomy 2q,"['trisomy 2qter', 'distal duplication 2q', 'distal trisomy type 2q', 'telomeric duplication 2q']",,,96094,,,,,,,,,
mondo:0019878,3q26 microduplication syndrome,"['dup(3q) syndrome', 'trisomy 3q26', 'Cornelia de Lange-like syndrome', 'dup(3)(q26)']",,,96095,CN206814,,,,,,,,
mondo:0019879,distal trisomy 4q,"['distal duplication 4q', 'distal trisomy type 4q', 'trisomy 4qter', 'telomeric duplication 4q']",,,96096,,,,,,,,,
mondo:0019880,distal trisomy 5q,"['distal trisomy type 5q', 'trisomy 5qter', 'distal duplication 5q', 'telomeric duplication 5q']",,,96097,,,,,,,,,
mondo:0019881,distal trisomy 6q,"['distal trisomy type 6q', 'trisomy 6qter', 'telomeric duplication 6q', 'distal duplication 6q']",,,96098,,,,,C537810,,,,
mondo:0019882,distal trisomy 8q,"['telomeric duplication 8q', 'distal duplication 8q', 'trisomy 8qter', 'distal trisomy type 8q']",,,96100,,,,,,,,,
mondo:0019883,distal trisomy 9q,"['telomeric duplication 9q', 'distal trisomy type 9q', 'distal duplication 9q', 'trisomy 9qter']",,,96101,,,,,,,,,
mondo:0019884,distal trisomy 10q,"['telomeric duplication 10q', 'distal trisomy type 10q', 'distal duplication 10q', 'trisomy 10qter']",,,96102,,,,,C538087,,,,
mondo:0019885,distal trisomy 11q,"['trisomy 11qter', 'distal duplication 11q', 'distal trisomy type 11q', 'telomeric duplication 11q']",,,96103,,,,,C538294,,,,
mondo:0019886,distal trisomy 13q,"['trisomy 13qter', 'telomeric duplication 13q', 'distal duplication 13q', 'distal trisomy type 13q']",,,96105,,,,,,,,,
mondo:0019887,distal trisomy 16q,"['distal duplication 16q', 'distal trisomy type 16q', 'telomeric duplication 16q', 'trisomy 16qter']",,,96106,,,,,,,,,
mondo:0019888,distal trisomy 20q,"['distal trisomy type 20q', 'telomeric duplication 20q', 'distal duplication 20q', 'trisomy 20qter']",,,96107,,,,,,,,,
mondo:0019889,distal trisomy 22q,"['trisomy 22qter', 'distal trisomy type 22q', 'distal duplication 22q', 'telomeric duplication 22q']",,,96109,,,,,,,,,
mondo:0019890,non-distal trisomy 9q,"['non-distal duplication 9q', 'non-telomeric trisomy 9q', 'non-distal trisomy type 9q']",,,96112,,,,,,,,,
mondo:0019891,monosomy 22,"['Del(22)', 'deletion 22', 'monosomy type 22']",,,96123,C0795878,,C36461,,,,,,
mondo:0019892,distal monosomy 7p,"['distal monosomy type 7p', 'distal deletion 7p', 'telomeric deletion 7p', 'monosomy 7pter']",,,96126,,,,,,,,,
mondo:0019893,distal monosomy 19p13.3,"['distal deletion 19p', 'telomeric deletion 19p']",,,96129,,,,,,,,,
mondo:0019895,distal monosomy 4q,"['monosomy 4qter', 'distal monosomy type 4q', 'telomeric deletion 4q', 'distal deletion 4q']",,,96145,,,,,,,,,
mondo:0019896,Kleefstra syndrome due to 9q34 microdeletion,"['9q subtelomeric deletion syndrome', '9qSTDS', 'Kleefstra syndrome due to 9q subtelomeric deletion', 'Kleefstra syndrome due to del(9)(q34)', 'Kleefstra syndrome due to monosomy 9q34']",,,96147,CN206831,,,,,,,,
mondo:0019897,distal monosomy 12q,"['monosomy 12qter', 'telomeric deletion 12q', 'distal deletion 12q', 'distal monosomy type 12q']",,,96149,,,,,,,,,
mondo:0019898,distal monosomy 14q,"['distal deletion 14q', 'distal monosomy type 14q', 'telomeric deletion 14q']",,,96150,,,,,,,,,
mondo:0019900,non-distal monosomy 12q,"['non-distal deletion 12q', 'non-distal monosomy type 12q', 'non-telomeric monosomy 12q']",,,96160,,,,,,,,,
mondo:0019901,non-distal monosomy 20q,"['non-telomeric monosomy 20q', 'non-distal monosomy type 20q', 'non-distal deletion 20q']",,,96164,,,,,,,,,
mondo:0019902,monosomy 13q34,"['monosomy type 13q34', 'distal deletion 13q34', 'Del(13)(q34)', 'subtelomeric deletion 13q34']",,,96168,,,,,,,,,
mondo:0019903,ring chromosome 2,"['rose cluster 2', 'chromosome 2 ring', 'Ring chromosome type 2', 'Ring 2', 'Ring chromosome 2 syndrome', 'R2']",,,96171,C4707448,,C121981,,,,,,
mondo:0019904,ring chromosome 3,"['rose cluster 3', 'Ring chromosome 3 syndrome', 'Ring chromosome type 3', 'R3', 'chromosome 3 ring', 'Ring 3']",,,96172,C4050314,,C121982,,,,,,
mondo:0019905,ring chromosome 9,"['Ring 9', 'chromosome 9 ring', 'Ring chromosome 9 syndrome', 'r9', 'Ring chromosome type 9']",,,96173,CN036105,,,,C538022,,,,
mondo:0019906,ring chromosome 11,"['Ring 11', 'Ring chromosome type 11', 'r11', 'r(11) syndrome', 'RC11', 'chromosome 11 ring', 'Ring chromosome 11 syndrome']",,,96175,C0265444,,,0002849,,758.89,,,
mondo:0019907,ring chromosome 13,"['Ring 13', 'R13', 'chromosome 13 ring', 'Ring chromosome 13 syndrome', 'Ring chromosome type 13']",,,96176,,,,,C538303,,,,
mondo:0019908,ring chromosome 15,"['Ring chromosome type 15', 'Ring 15', 'chromosome 15 ring', 'Ring chromosome 15 syndrome', 'R15']",,,96177,CN035931,,,,C538035,,,,
mondo:0019909,ring chromosome 16,"['R16', 'Ring 16', 'chromosome 16 ring', 'Ring chromosome type 16', 'Ring chromosome 16 syndrome']",,,96178,,,,,,,,,
mondo:0019910,maternal uniparental disomy of chromosome 2,"['maternal uniparental disomy of chromosome type 2', 'UPD(2)mat']",,,96179,,,,,,,,,
mondo:0019911,maternal uniparental disomy of chromosome 4,"['UPD(4)mat', 'maternal uniparental disomy of chromosome type 4']",,,96180,,,,,,,,,
mondo:0019912,maternal uniparental disomy of chromosome 6,"['UPD(6)mat', 'maternal uniparental disomy of chromosome type 6']",,,96181,,,,,,,,,
mondo:0019913,silver-Russell syndrome due to maternal uniparental disomy of chromosome 7,"['UPD(7)mat', 'Silver-Russell syndrome due to maternal uniparental disomy of chromosome type 7']",,,96182,CN206841,,,,,,,,
mondo:0019914,maternal uniparental disomy of chromosome 9,"['UPD(9)mat', 'maternal uniparental disomy of chromosome type 9']",,,96183,,,,,,,,,
mondo:0019915,maternal uniparental disomy of chromosome 14,"['UPD(14)mat', 'maternal uniparental disomy of chromosome type 14']",,,96184,,,,,,,,,
mondo:0019916,maternal uniparental disomy of chromosome 16,"['maternal uniparental disomy of chromosome type 16', 'UPD(16)mat']",,,96185,,,,,,,,,
mondo:0019917,maternal uniparental disomy of chromosome 20,"['uniparental disomy, maternal, chromosome 20', 'UPD(20)mat', 'maternal UPD(20)', 'maternal uniparental disomy of chromosome type 20', 'MULCHANDANI-BHOJ-CONLIN syndrome', 'MBCS']",0111714,617352,96186,,,,,,,,,
mondo:0019918,maternal uniparental disomy of chromosome 21,"['UPD(21)mat', 'maternal uniparental disomy of chromosome type 21']",,,96187,,,,,,,,,
mondo:0019919,maternal uniparental disomy of chromosome 22,"['UPD(22)mat', 'maternal uniparental disomy of chromosome type 22']",,,96188,,,,,,,,,
mondo:0019920,paternal uniparental disomy of chromosome 5,"['UPD(5)pat', 'paternal uniparental disomy of chromosome type 5']",,,96190,,,,,,,,,
mondo:0019921,paternal uniparental disomy of chromosome 6,"['paternal uniparental disomy of chromosome type 6', 'UPD(6)pat']",,,96191,,,,,,,,,
mondo:0019922,paternal uniparental disomy of chromosome 7,"['paternal uniparental disomy of chromosome type 7', 'UPD(7)pat']",,,96192,,,,,,,,,
mondo:0019923,Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome 11,"['Mosaic paternal uniparental disomy of chromosome 11', 'Beckwith-Wiedemann syndrome due to paternal uniparental disomy of chromosome type 11', 'UPD(11)pat']",,,96193,CN206842,,,,,,,,
mondo:0019924,paternal uniparental disomy of chromosome 20,"['UPD(20)pat', 'paternal UPD(20)', 'paternal uniparental disomy of chromosome type 20', 'paternal UPD20']",,,96194,C4275028,,,,,,,,
mondo:0019925,paternal uniparental disomy of chromosome 21,"['paternal uniparental disomy of chromosome type 21', 'UPD(21)pat']",,,96195,,,,,,,,,
mondo:0019926,X small rings,,,,96201,,,,,,,,,
mondo:0019927,growth hormone-producing pituitary gland neoplasm,"['growth hormone producing neoplasm of pituitary', 'growth hormone producing tumour of the pituitary', 'growth hormone secreting tumor of pituitary gland', 'growth hormone producing tumour of pituitary gland', 'growth hormone secreting neoplasm of pituitary gland', 'growth hormone producing tumor of pituitary', 'growth hormone producing neoplasm of pituitary gland', 'growth hormone producing pituitary gland tumor', 'growth hormone producing tumor of the pituitary', 'growth hormone secreting pituitary tumor', 'growth hormone-producing pituitary gland neoplasm', 'growth hormone producing tumor of the pituitary gland', 'growth hormone producing pituitary gland neoplasm', 'growth hormone producing tumour', 'growth hormone secreting tumour of pituitary', 'growth hormone secreting neoplasm of pituitary', 'growth hormone secreting pituitary gland neoplasm', 'growth hormone secreting pituitary gland tumor', 'growth hormone producing tumour of the pituitary gland', 'somatotropinoma of pituitary gland', 'growth hormone secreting neoplasm of the pituitary gland', 'growth hormone producing tumor', 'somatotropinoma', 'growth hormone secreting pituitary tumour', 'growth hormone secreting pituitary neoplasm', 'Growth hormone-producing pituitary gland tumor', 'pituitary somatotropinoma', 'growth hormone secreting pituitary gland tumour', 'growth hormone producing pituitary neoplasm', 'growth hormone producing tumor of pituitary gland', 'growth hormone producing neoplasm of the pituitary', 'Growth hormone-producing pituitary gland tumour', 'somatotropinoma of the pituitary', 'growth hormone producing pituitary gland tumour', 'growth hormone producing tumour of pituitary', 'growth hormone secreting tumour of the pituitary gland', 'growth hormone secreting tumour of pituitary gland', 'growth hormone secreting tumor of pituitary', 'growth hormone producing pituitary tumor', 'growth hormone secreting tumor of the pituitary', 'growth hormone secreting tumour of the pituitary', 'somatotroph tumour', 'somatotropinoma of the pituitary gland', 'growth hormone producing pituitary tumour', 'somatotropinoma of pituitary', 'pituitary gland somatotropinoma', 'somatotroph neoplasm', 'somatotroph tumor', 'growth hormone secreting tumor of the pituitary gland', 'growth hormone secreting neoplasm of the pituitary', 'growth hormone producing neoplasm of the pituitary gland']",,,,C0278864,,C7911,,,,,,
mondo:0019928,"48,XXXY syndrome","['XXXY syndrome', '48, XXXY syndrome']",,,96263,C0265498,,C89799,,,758.81,,10048228,
mondo:0019929,"49,XXXXY syndrome","['49,XXXXY', 'XXXXY syndrome']",,,96264,C0265499,,C185635,,D007713,758.81,,,
mondo:0019930,Leydig cell hypoplasia due to complete LH resistance,"['46,XY DSD due to complete LH resistance', '46,XY DSD due to complete luteinizing hormone resistance', 'Leydig cell hypoplasia due to complete luteinizing hormone receptor inactivation', '46,XY disorder of sex development due to complete LH resistance', '46,XY disorder of sex development due to complete luteinizing hormone receptor inactivation', 'Leydig cell hypoplasia due to complete LH receptor inactivation', 'Leydig cell hypoplasia due to complete luteinizing hormone resistance', '46,XY disorder of sex development due to complete luteinizing hormone resistance', '46,XY DSD due to complete LH receptor inactivation', '46,XY DSD due to complete luteinizing hormone receptor inactivation', '46,XY disorder of sex development due to complete LH receptor inactivation']",0112260,,96265,CN206847,"['-0.1582', '0.1235', '0.1266', '-0.00663', '0.11017', '-0.0742', '0.02301', '0.1616', '-0.02498', '-0.1613', '0.01813', '-0.07324', '-0.0406', '0.02539', '-0.0903', '-0.1334', '0.0376', '-0.0174', '-0.0354', '-0.256', '-0.05322', '-0.0753', '0.1537', '-0.0719', '0.0681', '0.03625', '-0.01627', '-0.01889', '0.007355', '-0.0872', '0.1482', '0.04993', '0.2152', '0.0481', '0.001034', '-0.1236', '0.00969', '0.014114', '-0.0773', '-0.2146', '0.04614', '-0.106', '0.0736', '-0.0457', '-0.07947', '-0.1399', '0.02005', '0.0267', '0.05606', '0.0361', '0.01559', '-0.0968', '0.1122', '0.0805', '-0.153', '0.03038', '0.1392', '-0.117', '-0.2483', '0.002771', '0.03772', '0.07043', '-0.0332', '0.04462', '0.02', '-0.0413', '0.1327', '0.1053', '-0.09467', '0.1929', '-0.03906', '0.02425', '0.08606', '-0.0784', '0.06354', '0.01247', '0.07544', '-0.10846', '-0.1399', '-0.07855', '-0.0909', '0.1218', '-0.02185', '0.0862', '-0.0716', '-0.0454', '0.0345', '0.1418', '0.247', '-0.04868', '0.05188', '0.1392', '-0.07916', '-0.08527', '0.2925', '0.01785', '0.07605', '-0.2502', '-0.01385', '0.1265']",,,,,,,
mondo:0019931,Leydig cell hypoplasia due to partial LH resistance,"['46,XY disorder of sex developement due to partial luteinizing hormone resistance', '46,XY DSD due to partial LH receptor inactivation', '46,XY DSD due to partial luteinizing hormone resistance', '46,XY DSD due to partial LH resistance', '46,XY disorder of sex developement due to partial LH resistance', '46,XY disorder of sex developement due to partial LH receptor inactivation', 'Leydig cell hypoplasia due to partial luteinizing hormone resistance', 'Leydig cell hypoplasia due to partial luteinizing hormone receptor inactivation', 'Leydig cell hypoplasia due to partial LH receptor inactivation']",0112261,,96266,CN206848,"['-0.1775', '0.1381', '0.11743', '-0.01227', '0.0672', '-0.0927', '0.03537', '0.1318', '-0.03647', '-0.1274', '-0.00953', '-0.09735', '-0.03397', '-0.00865', '-0.0647', '-0.11414', '0.04886', '-0.0446', '-0.003124', '-0.2446', '-0.062', '-0.0988', '0.1805', '-0.03885', '0.0643', '0.03616', '-0.02783', '-0.01335', '-0.004616', '-0.09845', '0.1595', '-0.0119', '0.1976', '0.06152', '-0.007145', '-0.07104', '0.0235', '0.02394', '-0.07715', '-0.1981', '0.02682', '-0.1153', '0.0762', '-0.03723', '-0.06793', '-0.1282', '0.0363', '0.01512', '0.02501', '0.05075', '0.00443', '-0.07587', '0.0791', '0.0706', '-0.2114', '0.02089', '0.1317', '-0.1375', '-0.2407', '0.05417', '0.02559', '0.07526', '-0.02263', '0.01397', '0.01408', '-0.02747', '0.1378', '0.0802', '-0.0748', '0.1956', '-0.05933', '0.0362', '0.1134', '-0.05582', '0.08', '0.02466', '0.0655', '-0.0902', '-0.1003', '-0.0604', '-0.0769', '0.1282', '-0.00877', '0.07996', '-0.0425', '-0.05716', '0.0434', '0.137', '0.2472', '-0.0512', '0.0471', '0.1356', '-0.0679', '-0.0719', '0.2815', '-0.02922', '0.08496', '-0.2556', '0.006878', '0.1066']",,,,,,,
mondo:0019932,isolated partial vaginal agenesis,['congenital absence of vagina'],,,96269,,,,,,,,,
mondo:0019933,acromegaly,"['Growth hormone excess', 'somatotroph adenoma', 'pituitary giant']",2449,,963,C0001206,,C84533,1001485,D000172,,,10000599,
mondo:0019934,polyploidy,,,,96321,,,,,D011123,,,,
mondo:0019935,isochromosome Y,['Isochromosome type Y'],,,96325,,,,,,,,,
mondo:0019938,anorectal malformation,,,,96346,,,,,C537771,751.5,,,
mondo:0019939,early-onset schizophrenia,,,,96369,,,,,,,,,
mondo:0019940,hypertrichosis-acromegaloid facial appearance syndrome,"['hypertrichosis-coarse face syndrome', 'haff', 'acromegaloid hypertrichosis syndrome', 'hypertrichosis-acromegaloid facial features syndrome', 'acromegaloid facial appearance syndrome and hypertrichosis']",,,966,CN226272,,,,,,,,
mondo:0019941,hereditary sensory and autonomic neuropathy type 2,"['HSAN2', 'neurogenic acroosteolysis', 'autosomal recessive sensory radicular neuropathy', 'hereditary sensory radicular neuropathy, recessive form', 'hereditary sensory neuropathy type 2', 'Giaccai type acroosteolysis', 'hereditary sensory and autonomic neuropathy type II']",0070161,,970,,"['0.815', '-0.0721', '-0.603', '0.6167', '-0.1366', '-0.488', '-0.4565', '0.4905', '-0.629', '0.1628', '0.339', '0.4907', '0.1407', '0.4814', '-0.8433', '0.669', '-0.1091', '0.7085', '-0.666', '-0.733', '0.4983', '-0.09937', '-0.4243', '0.6714', '-0.008095', '-0.0558', '-0.6294', '0.0672', '-0.2534', '-0.492', '0.7476', '-0.0402', '0.1438', '-0.0781', '-0.388', '-0.5127', '0.3435', '0.1202', '0.04163', '-0.282', '-0.5073', '-0.0894', '-0.3489', '-0.06366', '0.3801', '-0.4568', '0.2712', '0.1411', '0.1355', '0.4958', '-0.4524', '0.7617', '0.4062', '-0.931', '-0.233', '0.5967', '0.1335', '0.1', '-0.3276', '-0.3806', '0.1345', '0.642', '0.2817', '0.4282', '-0.1461', '0.3928', '0.2467', '0.57', '0.10406', '0.2026', '-0.8364', '0.08844', '-0.3274', '-0.2179', '0.787', '0.05774', '0.776', '0.779', '-0.587', '0.3474', '-0.05444', '-0.8677', '0.5347', '0.5557', '-0.4536', '0.02394', '0.4512', '-0.04926', '0.5693', '-0.615', '0.576', '0.2172', '0.382', '0.003252', '0.7715', '0.631', '-0.306', '-0.03662', '0.608', '0.548']",,,,,,,
mondo:0019942,distal arthrogryposis,['arthrogryposis multiplex congenita distal'],0050646,,97120,,"['-0.1197', '-0.05743', '0.2114', '-0.2522', '0.275', '-0.2026', '0.024', '0.1622', '-0.6733', '-0.03091', '-0.2013', '0.0762', '-0.4216', '0.3171', '-0.0843', '0.3704', '0.02841', '-0.1222', '-0.4126', '-0.847', '0.05283', '0.0364', '0.6772', '0.03014', '0.2235', '0.1494', '0.0779', '0.0829', '-0.1547', '-0.03506', '0.1508', '0.0284', '-0.03522', '0.3804', '0.368', '-0.0958', '-0.1426', '0.02844', '0.03668', '-0.08185', '-0.2008', '-0.3323', '-0.2288', '0.4285', '0.3923', '-0.223', '-0.192', '0.4553', '0.1444', '0.07117', '-0.4912', '-0.285', '0.2472', '-0.047', '-0.6', '-0.6733', '0.1584', '-0.1121', '-0.1747', '-0.609', '0.3726', '-0.1041', '-0.154', '0.1699', '-0.6733', '0.0174', '0.0725', '0.2449', '-0.3357', '0.02742', '-0.2922', '0.09033', '0.05856', '0.02573', '0.11755', '0.0986', '-0.062', '0.1788', '-0.4702', '-0.2856', '-0.1005', '-0.2223', '0.5566', '0.298', '-0.153', '-0.01541', '-0.0957', '0.4004', '-0.0219', '-0.3777', '0.2769', '0.3022', '0.1647', '0.2412', '0.4023', '0.2203', '0.621', '-0.5093', '0.0655', '0.3738']",,,,,,,
mondo:0019943,hereditary continuous muscle fiber activity,"['continuous muscle fiber activity hereditary', 'continuous muscle fibre activity hereditary']",,,972,C1834559,,,,,,,,
mondo:0019944,Eisenmenger syndrome,['Eisenmenger^s syndrome'],,,97214,C0013743,,C84390,,D004541,,,10058554,
mondo:0019945,solar urticaria,,,,97230,C0263610,,,,,708.8,L56.3,10041307,
mondo:0019946,ligneous conjunctivitis,['conjunctivitis lignosa'],,,97231,C1274789,,,,,372.39,,10071570,
mondo:0019947,rippling muscle disease 2,"['muscular dystrophy, limb-girdle, type IC', 'autosomal dominant limb-girdle muscular dystrophy caused by mutation in CAV3', 'LGMD1C', 'RMD2', 'limb-girdle muscular dystrophy due to caveolin-3 deficiency', 'limb-girdle muscular dystrophy type 1C', 'rippling muscle disease caused by mutation in CAV3', 'CAV3 rippling muscle disease', 'muscular dystrophy, limb-girdle, type 1C', 'muscular dystrophy limb-girdle type IC', 'rippling muscle disease 2', 'CAV3 autosomal dominant limb-girdle muscular dystrophy', 'rippling muscle disease type 2']",0060255,606072,97238,C1832560,"['-0.449', '-0.03302', '-0.003008', '-0.2435', '0.0814', '-0.2744', '0.06494', '0.3052', '-0.3518', '0.0265', '-0.204', '0.3677', '-0.1415', '-0.1305', '0.02686', '0.1613', '-0.131', '-0.1725', '-0.1941', '-0.7837', '0.3303', '-0.03226', '0.1337', '0.1562', '-0.1265', '-0.0692', '0.251', '-0.3113', '-0.08496', '-0.1204', '0.2068', '0.1284', '0.2493', '0.10944', '-0.1622', '-0.1461', '-0.1617', '0.011314', '0.07294', '-0.3452', '-0.06274', '-0.2722', '-0.07324', '0.2715', '0.05875', '0.03992', '-0.215', '0.2866', '0.1599', '0.3875', '-0.2683', '-0.154', '0.2133', '0.04095', '0.013504', '-0.2944', '0.286', '-0.1371', '-0.1049', '-0.07965', '0.2627', '0.219', '-0.0683', '-0.2783', '-0.4192', '-0.06793', '0.2986', '0.4724', '-0.3464', '0.0861', '-0.2325', '0.02628', '0.0634', '-0.0208', '0.1377', '0.01376', '0.02228', '0.0719', '-0.02913', '-0.2429', '0.2815', '0.01645', '0.1915', '0.06635', '-0.0635', '0.0453', '-0.11194', '0.2147', '0.454', '-0.02194', '0.1594', '0.1567', '0.1035', '0.1396', '0.3662', '0.2996', '0.2136', '-0.06537', '-0.3723', '0.0957']",C148325,,,,,,
mondo:0019948,reducing body myopathy,,0080090,,97239,,"['-0.3057', '0.191', '-0.4756', '0.502', '0.0848', '-0.654', '0.4683', '1.024', '-1.13', '-0.07025', '-0.527', '0.07745', '0.1853', '0.1071', '0.5566', '0.2263', '-0.2986', '0.4082', '-0.4912', '-0.7124', '0.2546', '-0.02304', '0.2151', '0.0792', '-0.2112', '0.0869', '-0.1776', '0.04153', '-0.5464', '0.172', '0.805', '0.05005', '0.3083', '-0.10803', '0.01707', '-0.1277', '-0.407', '-0.4683', '0.3455', '0.2493', '-0.02695', '-0.4685', '0.2764', '-0.07214', '0.04785', '0.1592', '-0.3416', '-0.1489', '-0.4397', '0.1615', '-0.1649', '-0.0377', '0.2329', '-0.04944', '0.006565', '-0.553', '-0.05765', '-0.069', '-0.1368', '-0.01811', '0.279', '-0.1724', '0.04514', '-0.05057', '-0.4602', '-0.03333', '0.317', '0.788', '-0.5596', '-0.08777', '-0.04504', '-0.2832', '0.07526', '-0.00348', '0.4426', '0.1252', '-0.5244', '0.3162', '-0.2952', '-0.2146', '0.3381', '0.385', '0.02304', '0.6133', '0.2343', '0.0838', '0.1278', '0.0668', '0.3813', '-0.1914', '0.4312', '-0.02603', '-0.1989', '0.402', '-0.03072', '0.1261', '0.6704', '-0.398', '0.2064', '-0.03119']",,,,359.89,,,
mondo:0019949,zebra body myopathy,,,,97240,C0270969,,,,,359.89,,,
mondo:0019950,congenital muscular dystrophy,"['MDC', 'congenital MD', 'CMD']",0050557,,97242,C0699743,,,0006819,,359.0,,,
mondo:0019951,rigid spine syndrome,"['rigid spine muscular dystrophy-1', 'rigid spine congenital muscular dystrophy', 'muscular dystrophy, congenital, merosin positive with early spine rigidity', 'desmin-related myopathies with Mallory bodies']",,,97244,,"['-0.5386', '0.397', '0.587', '-0.624', '0.07367', '-0.8', '0.3367', '0.615', '-0.807', '-0.4553', '-0.1389', '0.1754', '-0.459', '-0.02571', '0.2385', '-0.1525', '0.27', '-0.3474', '-0.4114', '-1.024', '0.0877', '-0.06323', '0.218', '0.2507', '-0.1709', '0.3474', '0.1032', '-0.2964', '-0.523', '-0.1844', '-0.07477', '0.3179', '-0.054', '-0.1846', '-0.1718', '-0.3274', '0.1462', '0.00617', '0.418', '-0.458', '0.01411', '-0.4646', '-0.158', '0.4434', '-0.0779', '0.1832', '-0.2717', '0.1589', '0.6226', '0.468', '-0.02713', '0.141', '0.403', '-0.2922', '-0.07556', '-0.6147', '0.5015', '0.3523', '0.2028', '-0.01831', '0.2257', '0.3628', '-0.3108', '0.1813', '-0.3374', '-0.1242', '0.2463', '0.7334', '-0.1715', '-0.1203', '-0.2186', '-0.0759', '0.4778', '-0.2448', '0.3298', '0.2357', '-0.0657', '0.3096', '-0.522', '-0.1727', '-0.02083', '-0.006687', '0.2793', '0.4353', '-0.4495', '0.015335', '-0.1866', '0.1476', '0.6436', '-0.1398', '-0.1427', '0.08307', '0.1506', '0.4895', '0.2761', '0.1164', '0.698', '-0.2399', '0.1677', '0.1687']",,,C535683,,,,
mondo:0019952,congenital myopathy,"['Batten Turner congenital myopathy', 'myopathy congenital']",0081337,,97245,,"['-0.633', '0.1225', '-0.1891', '-0.2832', '0.5044', '-0.4429', '0.1825', '0.666', '-1.05', '-0.1132', '0.2185', '0.0829', '-0.11664', '0.5103', '0.0478', '0.1946', '-0.775', '0.1711', '-0.5615', '-0.6675', '-0.009', '0.2925', '-0.4397', '0.1366', '0.1552', '-0.4214', '-0.002779', '-0.01262', '0.0476', '-0.0802', '0.12396', '-0.1685', '0.232', '0.133', '0.0358', '0.06107', '-0.384', '-0.1898', '-0.02597', '-0.542', '-0.4148', '-0.1543', '-0.33', '0.2126', '0.26', '-0.2622', '0.1954', '0.1836', '0.5586', '0.5547', '-0.467', '-0.6113', '0.2197', '-0.5146', '-0.2167', '-0.676', '-0.4053', '0.5015', '0.01845', '0.2642', '-0.2322', '-0.1921', '0.8022', '0.482', '-0.3215', '0.5747', '-0.1863', '0.7207', '-0.9336', '0.8447', '-0.2192', '0.177', '-0.2252', '-0.4092', '0.179', '-0.3066', '-0.032', '0.3271', '0.0877', '0.05124', '0.5464', '0.1714', '-0.006313', '0.06177', '0.135', '-0.03543', '-0.401', '0.144', '0.3647', '0.4194', '0.4966', '-0.557', '0.1772', '0.645', '0.1737', '0.1709', '-0.427', '-0.3271', '0.1355', '-0.381']",,,,,,10062547,
mondo:0019953,mega-cisterna magna,,,,97252,,,,,,,,,
mondo:0019954,pancreatic neuroendocrine tumor,"['neuroendocrine tumor of pancreas', 'islet cell tumours of the pancreas', 'well differentiated pancreatic endocrine tumor', 'PANET', 'well differentiated pancreatic endocrine tumour', 'islet cell tumor', 'pancreatic neuroendocrine tumor', 'well-differentiated NEN of pancreas', 'islet cell tumors of the pancreas', 'neuroendocrine tumour of pancreas', 'pancreatic endocrine tumour', 'well-differentiated pancreatic neuroendocrine neoplasm', 'well-differentiated pancreatic NEN', 'islet cell tumour', 'pancreatic endocrine tumor', 'well differentiated pancreatic endocrine neoplasm', 'well-differentiated neuroendocrine neoplasm of pancreas', 'islet cell tumors - pancreas', 'islet cell tumours - pancreas', 'pancreatic NET']",,,97253,,,C27720,1000045,,,,,
mondo:0019955,GRFoma,"['GRF tumour', 'Growth hormone releasing factor tumour', 'Growth hormone releasing factor tumor', 'GRF tumor']",,,97261,CN206877,,,,,,,,
mondo:0019956,encephalitis,['brain inflammation'],9588,,97275,C0014038,,C26760,,D004660,323.9,A85,10014581,
mondo:0019957,PPoma,"['pancreatic polypeptide neoplasm', 'pancreatic polypeptide tumor', 'pancreatic polypeptide tumour', 'pancreatic polypeptidoma']",,,97278,CN206879,,C67453,,,239.89,,,
mondo:0019959,glucagonoma,"['glucagonoma', 'glucagonoma syndrome', 'pancreatic glucagonoma']",,,97280,C0017689,,C95597,1000441,D005935,,,10018404,
mondo:0019960,VIPoma,"['VIP-producing neuroendocrine tumor', 'vasoactive intestinal peptide-secreting tumor', 'VIPoma', 'pancreatic cholera', 'vasoactive intestinal peptide-producing tumour', 'Verner-Morrison syndrome', 'VIP-secreting tumour', 'vasoactive intestinal peptide producing tumor', 'watery diarrhea-hypokalemia-achlorhydria syndrome', 'malignant vasoactive intestinal peptide-secreting tumor', 'VIP-producing neuroendocrine tumour', 'VIP-secreting tumor', 'vasoactive intestinal peptide producing neoplasm', 'Diarrheogenic islet cell tumor', 'VIP- secreting tumor', 'VIP- secreting tumour', 'WDHA syndrome', 'VIP producing neoplasm', 'malignant vasoactive intestinal peptide-secreting tumour', 'VIP-producing NET', 'Diarrheogenic islet cell tumour', 'vasoactive intestinal peptide-secreting tumour', 'vasoactive intestinal peptide producing tumour', 'vasoactive intestinal peptide (VIP) tumor', 'vasoactive intestinal peptide (VIP) tumour', 'vasoactive intestinal peptide-producing tumor', 'watery diarrhea, hypokalemia, and achlorhydria syndrome', 'pancreatic vipoma', 'VIP- secreting neoplasm', 'vasoactive intestinal peptide secreting neoplasm', 'VIPoma, malignant']",5574,,97282,C0011993,,C26749,1000622,D003969,239.7,,10047430,
mondo:0019962,thyroid lymphoma,"['lymphoma of thyroid gland', 'thyroid lymphoma', 'lymphoma of thyroid', 'lymphoma of the thyroid', 'primary thyroid gland lymphoma', 'lymphoma of the thyroid gland', 'thyroid gland lymphoma']",10011,,97285,C1336753,,C5265,,,,,,
mondo:0019963,bronchial endocrine tumor,"['bronchus neuroendocrine neoplasm', 'bronchus NET', 'bronchus neuroendocrine tumor, well differentiated, low or intermediate grade', 'bronchial neuroendocrine tumor', 'bronchus neuroendocrine tumour', 'bronchus neuroendocrine tumor', 'neuroendocrine neoplasm of bronchus', 'bronchial neuroendocrine tumour', 'bronchial NET']",,,97287,CN206886,,,,,,,,
mondo:0019964,thymic neuroendocrine tumor,"['thymus neuroendocrine tumor', 'thymus neuroendocrine tumour', 'thymus neuroendocrine neoplasm', 'neuroendocrine neoplasm of thymus', 'thymus NET', 'thymus neuroendocrine tumor, well differentiated, low or intermediate grade']",,,97289,CN206887,,,,,,,,
mondo:0019967,Kienbock disease,"['aseptic necrosis of the lunate bone', 'Lunatomalacia', 'Osteochondrosis of the lunate bone', 'bilateral Kienbock^s disease', 'Kienbock^s disease', 'osteochondritis of the lunate bone']",,,97332,,,,,,,,10064242,
mondo:0019969,panner disease,"['Osteochondrosis of the capital humerus', 'aseptic necrosis of the capital humerus']",,,97336,CN206896,,,,,,,,
mondo:0019970,Sinding-Larsen-Johansson disease,"['aseptic necrosis of patella', 'Osteochondrosis of patella']",,,97337,CN206897,,,,,,,10063585,
mondo:0019971,melanoma of soft tissue,['clear cell sarcoma of the tendons and aponeuroses'],,,97338,C0206651,,,,,,,,
mondo:0019972,dural sinus malformation,"['cranial dural arteriovenous malformations', 'cranial dural arteriovenous fistula']",,,97339,,,,,,,,,
mondo:0019973,persistent placoid maculopathy,,,,97341,C4304823,,,,,,,,
mondo:0019975,pellagra,"['niacin-tryptophan deficiency', 'pellagra', 'niacin deficiency']",8457,,97352,C4317126,,,0008570,D010383,265.2,,10029400,
mondo:0019976,dementia pugilistica,"['punch-drunk syndrome', 'Boxer^s dementia', 'chronic traumatic encephalopathy']",0081291,,97353,CN206907,,,,D020208,,,,
mondo:0019977,parkinsonism with dementia of Guadeloupe,,,,97355,CN206908,,,,,,,,
mondo:0019978,Robinow syndrome,"['Robinow dwarfism', 'Robinow-Silverman-Smith syndrome', 'acral dysostosis with facial and genital abnormalities', 'Covesdem syndrome (formerly)', 'mesomelic dwarfism-small genitalia syndrome', 'costovertebral segmentation defect with mesomelia (formerly)', 'fetal face syndrome', 'foetal face syndrome']",0060254,,97360,CN776872,"['0.07025', '0.3062', '0.4502', '-0.7095', '0.4993', '-0.1725', '-0.004368', '0.9937', '-0.3503', '-0.3975', '-0.2064', '-0.01958', '-0.476', '0.535', '0.3118', '0.595', '0.305', '-0.1725', '-0.02353', '-0.304', '-0.5723', '0.06076', '0.8003', '-0.3376', '0.02657', '-0.278', '-0.1926', '-0.3057', '0.834', '-0.656', '0.4746', '-0.1587', '-0.02586', '-0.8286', '0.0897', '-0.04385', '-0.3984', '-0.4312', '0.1251', '-0.0448', '0.1445', '-0.2588', '0.28', '-0.1768', '0.4534', '-0.1946', '0.0941', '0.3083', '-0.0834', '0.32', '-0.1017', '-0.2878', '-0.405', '-0.4731', '-0.04425', '-0.8027', '0.002216', '-0.2306', '0.1288', '0.311', '0.1293', '-0.014694', '-0.4434', '0.338', '0.5215', '0.1427', '0.08624', '0.1443', '-0.198', '0.4983', '-0.52', '0.663', '0.4521', '-0.3289', '0.1337', '0.848', '0.1692', '-0.4224', '-0.6', '-0.0264', '-0.0865', '0.3315', '-0.04865', '0.6436', '-0.3545', '0.6006', '0.0802', '-0.4539', '0.08905', '-0.1225', '-0.05365', '0.2223', '-0.0651', '-0.1192', '0.6475', '0.04282', '0.2225', '-0.522', '0.1342', '-0.08276']",C85048,,,,,,
mondo:0019979,"renal hypoplasia, unilateral",,,,97361,,,,,,,Q60.3,,
mondo:0019980,"renal hypoplasia, bilateral",,,,97362,,,,,,,Q60.4,,
mondo:0019981,unilateral multicystic dysplastic kidney,"['unilateral multicystic renal dysplasia', 'unilateral MCDK']",,,97363,,,,,,,,,
mondo:0019982,bilateral multicystic dysplastic kidney,"['MRD', 'Pelvi-ureteric junction obstruction', 'PUJO', 'bilateral MCDK', 'bilateral multicystic renal dysplasia']",,,97364,,,,,,,,,
mondo:0019983,multiloculated renal cyst,"['multilocular cyst of the kidney', 'multilocular renal cyst']",,,97366,,,,,,,,,
mondo:0019984,renal tubular dysgenesis due to twin-twin transfusion,,,,97367,CN206914,,,,,,,,
mondo:0019985,drug-related renal tubular dysgenesis,,,,97368,,,,,,,,,
mondo:0019986,sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy,,,,97555,CN206920,,,,,,,,
mondo:0019988,pauci-immune glomerulonephritis with ANCA,['pauci-immune glomerulonephritis with antineutrophil cytoplasmic antibody'],,,97563,CN206923,,,,,,,,
mondo:0019989,pauci-immune glomerulonephritis without ANCA,"['pauci-immune glomerulonephritis without antineutrophil cytoplasmic antibody', 'antineutrophil cytoplasmic antibody-negative pauci-immune glomerulonephritis']",,,97564,,,,,,,,,
mondo:0019990,non-amyloid fibrillary glomerulopathy,"['non-amyloid fibrillary glomerulonephritis', 'fibrillary glomerulonephritis', 'Congo red-negative amyloidosis-like glomerulopathy']",,,97566,C4273674,,,,,,,,
mondo:0019991,immunotactoid glomerulopathy,"['fibrillary glomerulonephritis', 'Immunotactoid glomerulonephritis', 'FGN']",,,97567,,,C96182,,,583.9,,,
mondo:0019992,pseudohypoparathyroidism,,4184,,97593,C0033806,,C99027,,D011547,275.49,E20.1,10037126,
mondo:0019993,congenital renal artery stenosis,"['congenital renovascular hypoplasia', 'congenital RAS']",,,97598,,,,,,,Q27.1,,
mondo:0019994,maternal uniparental disomy of chromosome 13,"['maternal uniparental disomy of chromosome type 13', 'UPD(13)mat']",,,97678,CN036719,,,,,,,,
mondo:0019995,peripheral resistance to thyroid hormones,,,,97927,CN206931,"['-0.246', '0.3403', '0.05383', '0.07764', '0.09143', '0.07263', '0.1515', '0.02652', '-0.06094', '-0.33', '0.07336', '-0.0316', '0.0651', '0.2927', '0.08875', '-0.3696', '-0.0748', '0.01332', '-0.3608', '-0.585', '0.1447', '-0.2358', '0.1761', '-0.446', '-0.006927', '-0.001277', '-0.0486', '-0.1586', '0.1844', '-0.3232', '0.263', '0.2372', '-0.01065', '0.0179', '-0.249', '-0.0738', '0.06714', '0.1544', '-0.0837', '-0.078', '0.05737', '0.093', '0.1075', '0.1625', '-0.01938', '-0.2477', '0.5435', '-0.0373', '0.363', '0.1527', '0.08514', '-0.005997', '0.2335', '0.1986', '-0.362', '0.1489', '0.4258', '-0.562', '-0.0649', '0.0914', '0.1489', '0.013374', '-0.11066', '0.1249', '-0.2668', '0.2395', '0.341', '0.5557', '-0.393', '0.1462', '-0.1926', '0.2969', '0.1506', '-0.3757', '0.2646', '0.11584', '0.07983', '0.0864', '-0.10596', '-0.1168', '-0.3694', '-0.03278', '-0.1697', '-0.07635', '-0.08124', '-0.1009', '0.2346', '-0.162', '0.5', '-0.05356', '0.2622', '0.1831', '-0.1436', '-0.038', '0.603', '0.05438', '0.0742', '-0.03528', '-0.01419', '0.3765']",,,,,,,
mondo:0019998,gastroduodenal malformation,,,,97944,,,,,,,,,
mondo:0019999,intestinal malformation,,,,97945,,,,,,,,,
mondo:0020001,respiratory or thoracic malformation,,,,97957,,,,,,,,,
mondo:0020007,absence of the pulmonary artery,,,,980,CN206941,,,,,,,,
mondo:0020010,infectious disorder of the nervous system,"['nervous system infectious disease', 'nervous system infectious disorder']",,,98010,C0597039,,C27590,,,349.89,,,
mondo:0020018,cranial malformation,,,,98038,,,,,,,,,
mondo:0020019,digestive tract malformation,,,,98039,,,,,,,,,
mondo:0020020,"visceral malformation of the liver, biliary tract, pancreas or spleen",,,,98041,,,,,,,,,
mondo:0020022,central nervous system malformation,,,,98044,,,,,D009421,,Q00-Q07,,
mondo:0020023,respiratory or mediastinal malformation,,,,98045,,,,,,,,,
mondo:0020039,"46,XX disorder of sex development induced by androgens excess","['46,XX DSD induced by androgens excess']",,,98078,CN227738,,,,,,,,
mondo:0020040,"46,XY disorder of sex development","['XY female', '46, XY disorders of sexual development', '46,XY disorders of Sex development', '46,XY DSD', '46, XY female', '46,XY differences of Sex development', '46, XY DSD']",,,98085,C2751824,,C127171,,D058490,,,,
mondo:0020043,autosomal recessive congenital cerebellar ataxia,,,,98095,,,,,,,,,
mondo:0020044,autosomal recessive metabolic cerebellar ataxia,,,,98096,CN229258,,,,,,,,
mondo:0020046,autosomal recessive degenerative and progressive cerebellar ataxia,,,,98098,CN229259,,,,,,,,
mondo:0020047,autosomal recessive syndromic cerebellar ataxia,,,,98099,CN227742,,,,,,,,
mondo:0020048,internal carotid agenesis,"['agenesis of the internal carotid artery', 'internal carotid artery agenesis']",,,981,,,,,,,,,
mondo:0020049,autosomal anomaly,"['chromosomal anomaly of autosome', 'autosome chromosomal anomaly']",,,98127,CN227743,,,,,,,,
mondo:0020058,gonosome anomaly,['Sex-chromosome anomaly'],,,98155,,,,,,758.81,,,
mondo:0020064,pulmonary valve agenesis,"['congenital absence of the pulmonary valve', 'absent pulmonary valve syndrome', 'PVA', 'pulmonary valves agenesis']",,,982,,,,,,,,,
mondo:0020065,combined dystonia,['dystonia-plus syndrome'],,,98203,CN206969,,,,,,,,
mondo:0020066,Ehlers-Danlos syndrome,"['Disease, Ehlers-Danlos', 'skin elastic', 'Ehlers-Danlos syndromes', 'Ehlers Danlos syndrome', 'danlos ehlers syndrome', 'Hereditary collagen dysplasia', 'Fibrodysplasia elastica generalisata', 'ED syndrome', 'Meekeren-Ehlers-Danlos syndrome', 'Danlos disease', 'Ehlers Danlos Disease', 'Syndrome, Ehlers-Danlos', 'elastic skin', 'Ehler Danlos Syndrome', 'Danlos Disease, Ehlers', 'EDS', 'Ehlers-Danlos Disease', 'Disease, Ehlers Danlos', 'Dystrophia mesodermalis congenita']",13359,,98249,C0013720,,C34568,,D004535,756.83,Q79.6,10014316,
mondo:0020067,infectious encephalitis,['encephalitis infection'],,,,,,C79550,,D000069544,323.4,,,
mondo:0020068,postinfectious encephalitis,,10993,,98253,C0393459,,,,,323.6,,10057235,
mondo:0020069,chronic encephalitis,"['encephalitis, chronic']",,,98255,C0006109,,,,,,,,
mondo:0020070,neonatal epilepsy syndrome,,,,98257,CN206974,,,,,,,,
mondo:0020071,infantile epilepsy syndrome,"['infantile onset epilepsy syndrome', 'epilepsy syndrome of infancy']",,,98258,CN206975,,,,,,,,
mondo:0020072,childhood-onset epilepsy syndrome,"['childhood epilepsy syndrome', 'epilepsy syndrome of childhood', 'pediatric epilepsy syndrome', 'paediatric epilepsy syndrome']",,,98259,CN206976,,,,,,,,
mondo:0020073,adolescent-onset epilepsy syndrome,,,,98260,CN206977,,,,,,,,
mondo:0020074,progressive myoclonus epilepsy,"['progressive myoclonic epilepsy (disorder) [ambiguous]', 'progressive myoclonic epilepsy', 'epilepsy, progressive myoclonic', 'progressive myoclonus epilepsy', 'PME', 'familial progressive myoclonic epilepsy']",891,,98261,C0751778,"['0.836', '0.03035', '-0.186', '-0.1453', '-0.4312', '-0.4023', '0.919', '0.379', '-0.6777', '-0.495', '-0.01944', '-0.337', '-0.412', '0.533', '-0.0505', '0.0769', '-0.3418', '-0.6074', '-0.4883', '-0.443', '-0.1921', '0.5317', '0.1754', '-0.4163', '-0.2073', '0.02419', '0.0144', '-0.10095', '-0.626', '0.354', '0.3057', '-0.684', '0.1406', '0.2218', '0.8506', '0.563', '-0.05084', '-0.1498', '-0.0757', '-0.5176', '-0.0717', '-0.501', '0.11127', '-0.393', '-0.4592', '-0.823', '-0.2947', '0.2433', '0.7417', '0.67', '-0.2443', '0.0825', '0.02946', '-0.541', '0.1648', '-0.2378', '-0.2974', '0.0745', '-0.2207', '0.3694', '-0.689', '0.555', '0.6904', '-0.346', '-0.4062', '1.598', '0.1768', '0.06055', '-1.02', '0.816', '1.029', '1.035', '-0.03403', '-0.5034', '0.157', '0.7944', '1.041', '0.3655', '-0.3218', '0.414', '-0.0591', '0.8857', '0.359', '0.3909', '0.2568', '0.2006', '0.1357', '0.807', '0.7324', '0.322', '-0.03366', '0.2052', '-0.306', '0.0671', '0.1553', '0.3286', '0.345', '-0.54', '0.1343', '0.3367']",C7636,,D020191,,,,
mondo:0020075,hereditary non-syndromic obesity,"['monogenic obesity due to a leptin-melanocortin pathway anomaly', 'genetic non-syndromic obesity']",,,98267,,,,,,,,,
mondo:0020076,myeloproliferative neoplasm,"['myeloproliferative neoplasm, chronic', 'MPD', 'myeloproliferative neoplasm', 'CMPD', 'myeloproliferative disorder', 'CMPD, U', 'myeloproliferative tumor', 'chronic myeloproliferative disease', 'chronic myeloproliferative disorders', 'MPN', 'chronic myeloproliferative disorder', 'chronic myeloproliferative neoplasm', 'myeloproliferative tumour', 'myeloproliferative neoplasms']",2226,,98274,C1292778,"['-0.2408', '0.1895', '0.08307', '-0.1481', '0.0356', '-0.10785', '0.1667', '0.293', '0.0291', '0.0792', '0.1305', '-0.1421', '-0.03937', '-0.03116', '-0.1807', '-0.1969', '-0.1005', '-0.2382', '0.1366', '-0.293', '-0.09265', '-0.3843', '0.4238', '-0.3208', '0.1786', '-0.1284', '-0.0311', '-0.2507', '-0.2117', '-0.2192', '-0.02798', '0.10443', '0.313', '-0.00685', '0.12177', '-0.07446', '-0.3606', '-0.2205', '-0.05304', '-0.3906', '-0.02504', '-0.08466', '0.09174', '-0.3474', '-0.12305', '-0.238', '-0.2576', '0.00996', '0.2776', '-0.1117', '0.1721', '-0.08', '0.138', '0.3025', '-0.02231', '-0.05124', '0.1832', '-0.0676', '-0.4912', '0.0762', '0.0569', '0.03656', '-0.02153', '-0.1481', '0.03723', '-0.13', '0.2156', '0.1043', '-0.0215', '0.2847', '0.1812', '-0.1862', '-0.1393', '0.0721', '-0.006504', '0.04736', '-0.01611', '0.0672', '0.002457', '-0.261', '-0.348', '-0.2026', '-0.1367', '0.07', '-0.3306', '-0.12463', '0.2257', '0.3064', '0.2411', '-0.05054', '0.1523', '-0.00996', '-0.2014', '-0.1936', '0.4753', '0.1262', '0.252', '-0.4402', '-0.1256', '0.0199']",C4345,0004251,,238.79,,10028576,
mondo:0020077,myelodysplastic/myeloproliferative disease,,,,98275,,,,,D054437,,,,
mondo:0020081,macrophage or histiocytic tumor,,,,98288,CN206983,,,,,,,,
mondo:0020082,dendritic cell tumor,"['Dendritic cell sarcoma, NOS', 'Dendritic cell neoplasm', 'Dendritic cell tumor, NOS', 'Dendritic cell tumor, Not otherwise specified', 'Dendritic cell sarcoma, Not otherwise specified']",,,98289,CN206984,,C27260,,,,,,
mondo:0020083,immunodeficiency-associated lymphoproliferative disease,,,,98290,CN206985,,,,,,,,
mondo:0020084,lymphoproliferative disease associated with primary immune disease,,,,98291,CN206986,,,,,,,,
mondo:0020087,hereditary lipodystrophy,"['genetic lipodystrophy (disease)', 'genetic lipodystrophy']",,,98305,C4511302,,,,,,,,
mondo:0020088,familial partial lipodystrophy,"['FPLD', 'Koberling-Dunnigan syndrome', 'congenital partial lipodystrophy', 'lipodystrophy, familial partial', 'genetic partial lipodystrophy']",0050440,,98306,C0271694,"['0.802', '0.03018', '-0.1156', '-0.1788', '0.363', '-0.5396', '0.336', '0.4038', '0.1947', '-0.3123', '-0.8125', '-0.388', '0.3093', '0.3132', '-0.3877', '0.0212', '0.05826', '0.1344', '-0.1343', '-0.3843', '-0.4045', '-0.773', '0.6016', '0.002121', '-0.1589', '0.11694', '0.4587', '0.02344', '0.431', '-0.7944', '1.574', '-0.2397', '0.298', '0.02954', '-0.4792', '0.352', '-0.02856', '0.2274', '-0.03992', '0.02805', '-0.3682', '-0.213', '0.4487', '0.638', '0.6304', '-0.1667', '-0.04282', '-0.2034', '0.2861', '0.1077', '-0.1339', '0.061', '0.1084', '0.1497', '-0.009796', '-0.5225', '0.3953', '-0.4802', '-0.5806', '-0.3643', '0.0619', '0.08844', '0.1257', '-0.6606', '-0.5015', '0.501', '-0.3022', '0.1731', '-0.52', '-0.00588', '-0.1073', '0.1653', '0.3167', '0.16', '0.7686', '-0.3623', '0.02187', '0.2222', '-0.2399', '-0.3638', '-0.417', '0.21', '0.1218', '0.0628', '-0.07513', '0.555', '0.11084', '-0.3464', '0.3958', '0.0852', '0.4878', '0.2915', '-0.2327', '0.3372', '0.385', '-0.606', '0.839', '-0.3098', '-0.2952', '-0.3088']",C84708,,D052496,,,,
mondo:0020089,acquired lipodystrophy,['acquired lipodystrophy (disease)'],,,98307,C0877192,,,,,,,10049287,
mondo:0020093,autosomal dominant isolated diffuse palmoplantar keratoderma,"['isolated diffuse palmoplantar keratoderma, autosomal dominant', 'autosomal dominant isolated diffuse palmoplantar hyperkeratosis']",,,98349,CN229268,,,,,,,,
mondo:0020096,autosomal recessive isolated diffuse palmoplantar keratoderma,"['autosomal recessive isolated diffuse palmoplantar hyperkeratosis', 'isolated diffuse palmoplantar keratoderma, autosomal recessive']",,,98356,CN229269,,,,,,,,
mondo:0020099,inherited sideroblastic anemia,"['constitutional sideroblastic anemia', 'constitutional sideroblastic anaemia']",,,98362,,,,,,,,,
mondo:0020102,hereditary stomatocytosis,['hereditary stomatocytic disease'],,,98365,C1262483,,,,,282.8,,,
mondo:0020108,autoimmune hemolytic anemia,"['idiopathic autoimmune hemolytic anaemia', 'acquired autoimmune hemolytic anemia', 'idiopathic autoimmune hemolytic anemia', 'familial auto-immune hemolytic anaemia (subtype)', 'anaemia hemolytic autoimmune', 'AHA', 'anemia, autoimmune hemolytic', 'immuno-hemolytic anaemia', 'autoimmune haemolytic anemia', 'familial auto-immune hemolytic anemia (subtype)', 'acquired autoimmune hemolytic anaemia', 'autoimmune haemolytic anaemia', 'autoimmune hemolytic anemia', 'AIHA', 'anemia hemolytic autoimmune', 'immuno-hemolytic anemia']",718,205700,98375,C0002880,,C34378,1001264,D000744,283.0,,10002046,
mondo:0020110,pulmonary agenesis,"['congenital lung agenesis', 'unilateral lobar pulmonary agenesis', 'unilateral lung agenesis', 'congenital absence of lung']",,,984,C0265780,,C99028,,C562992,748.5,,10037322,
mondo:0020112,vitamin B12- and folate-independent constitutional megaloblastic anemia,,,,98415,,,,,,,D53.0,,
mondo:0020113,primary acquired red cell aplasia,"['primary autoimmune red cell aplasia', 'red cell aplasia']",,,98421,C0034902,,,,,,,10038184,
mondo:0020115,secondary polycythemia,"['secondary erythrocytosis', 'secondary polycythemia']",,,98428,C1318533,,C27178,,,,,10036062,
mondo:0020117,alpha granule disease,,,,98455,CN207009,,,,,,,,
mondo:0020118,dense granule disease,['Delta granule disease'],,,98456,CN207010,,,,,,,,
mondo:0020119,X-linked syndromic intellectual disability,"['mental retardation, X-linked syndromic', 'syndromic X-linked intellectual disability', 'syndromic X-linked mental retardation', 'syndromic intellectual disability, X-linked', 'intellectual disability, X-linked syndromic']",0060309,,98464,,"['-0.0669', '0.1637', '0.0368', '-0.1868', '0.1153', '-0.279', '0.00866', '0.2147', '-0.1147', '-0.2288', '-0.0676', '-0.006844', '0.06018', '-0.09375', '0.0842', '-0.02505', '0.005886', '0.001628', '-0.1481', '-0.4517', '-0.00761', '0.0777', '0.09546', '-0.0831', '0.1279', '-0.04318', '-0.02077', '-0.1014', '0.06525', '-0.1643', '0.201', '0.011566', '0.268', '0.0678', '0.0083', '-0.1335', '-0.0674', '-0.2761', '-0.1149', '-0.2107', '0.11444', '-0.2263', '-0.05', '-0.12146', '-0.03232', '-0.2983', '-0.00819', '0.02191', '-0.02148', '-0.0159', '-0.0492', '-0.03348', '-0.01822', '-0.1406', '-0.05667', '-0.02788', '0.1729', '-0.03894', '-0.0839', '0.09424', '0.099', '-0.04974', '0.1403', '0.08417', '-0.0383', '0.0782', '0.07513', '0.2578', '-0.2074', '0.1744', '-0.2644', '-0.036', '0.009445', '-0.11914', '0.1129', '0.1225', '0.10297', '0.0006886', '-0.1791', '-0.052', '-0.007526', '0.1359', '-0.1318', '0.3079', '0.05258', '0.1335', '0.03168', '0.2319', '0.1177', '0.2065', '0.0927', '0.312', '-0.02702', '0.082', '0.4807', '0.0978', '0.1649', '-0.251', '0.2397', '0.05087']",,,,,,,
mondo:0020120,skeletal muscle disorder,"['disease of skeletal muscle tissue', 'skeletal muscle tissue disease or disorder', 'disorder of skeletal muscle tissue', 'skeletal muscle tissue disease']",,,98472,C1533847,,,,D009135,,,10028641,
mondo:0020121,muscular dystrophy,,9884,,98473,C0026850,,C84910,,D009136,359.1,G71.0,10028356,
mondo:0020122,acquired idiopathic inflammatory myopathy,"['IIm', 'idiopathic inflammatory myopathy, familial', 'idiopathic inflammatory myopathies', 'idiopathic inflammatory myositis', 'IMM']",,,98482,,,,,,359.79,,,
mondo:0020123,metabolic myopathy,,,,98486,C0270984,,C98985,,,359.89,,10068836,
mondo:0020124,neuromuscular junction disease,,439,,98495,C0751950,,,,D020511,,,,
mondo:0020125,acquired neuromuscular junction disease,['acquired neuromuscular junction disease'],,,98494,CN207015,,,,,,,,
mondo:0020127,hereditary peripheral neuropathy,['genetic peripheral neuropathy'],,,98497,,,,,,,,,
mondo:0020128,motor neuron disorder,"['anterior horn cell disease', 'disorder of motor neuron', 'motor neuron disease or disorder', 'motor neuron disease', 'disease of motor neuron']",231,,98503,,,,0003782,D016472,335.9,G12.2,10028003,
mondo:0020129,acquired motor neuron disease,"['acquired anterior horn cell disease', 'acquired motor neuron disease']",,,98506,CN207019,,,,,,,,
mondo:0020130,malformation of the cerebellar vermis,,,,98514,,,,,,,,,
mondo:0020131,malformation of the cerebellar hemispheres,,,,98516,,,,,,,,,
mondo:0020132,cranial nerve and nuclear aplasia,,,,98518,,,,,,,,,
mondo:0020133,posterior fossa malformation,,,,98519,,,,,,,,,
mondo:0020134,cystic malformation of the posterior fossa,,,,98520,,,,,,742.4,,,
mondo:0020135,pontocerebellar hypoplasia,"['nonsyndromic pontocerebellar hypoplasia', 'isolated pontocerebellar hypoplasia', 'pontocerebellar hypoplasia', 'pontoneocerebllar hypoplasia', 'PCH', 'pontoneocerebellar atrophy']",0060264,,98523,CN924922,"['0.193', '0.3047', '-0.1968', '-0.1526', '0.43', '-0.5327', '0.3162', '0.2046', '-0.7627', '-0.3132', '-0.615', '-0.8555', '-0.2334', '-0.2437', '0.544', '0.3655', '0.02785', '-0.1565', '-0.00779', '-0.912', '-0.1096', '-0.3542', '0.543', '-0.249', '-0.03036', '-0.121', '0.09674', '-0.11633', '-0.02869', '-0.3408', '0.5166', '0.528', '-0.1898', '-0.2876', '-0.04437', '0.2341', '0.1862', '-0.1396', '-0.0989', '0.06158', '0.1648', '-0.5146', '0.2546', '0.4429', '0.1564', '-0.5034', '-0.1163', '0.07666', '-0.1747', '0.568', '0.03513', '-0.1094', '0.06793', '-0.2449', '0.2141', '-0.2544', '-0.0945', '0.2301', '-0.2087', '0.3618', '0.16', '0.0918', '0.406', '0.3206', '-0.5674', '0.23', '0.2002', '0.642', '-0.4875', '0.4673', '0.1282', '0.0699', '-0.2656', '0.1142', '0.451', '-0.1337', '0.628', '-0.3132', '-0.736', '-0.3105', '0.02176', '0.1141', '0.04663', '0.7725', '-0.09247', '0.1309', '-0.0203', '0.418', '0.1644', '-0.5874', '0.5063', '0.2285', '0.05127', '0.02155', '0.52', '0.3435', '0.872', '0.3538', '0.512', '-0.3203']",,,C580383,,,,
mondo:0020143,cerebral lipidosis with dementia,['cerebral lipidosis'],10742,,98544,C0007788,,,,,330.1,,,
mondo:0020144,cerebrovascular dementia,['rare cerebrovascular dementia'],,,98549,,,,,,,,,
mondo:0020145,developmental defect of the eye,,,,98553,,,,,,,,,
mondo:0020146,major induction processes eye anomaly,,,,98554,,,,,,,,,
mondo:0020147,anophthalmia-microphthalmia syndrome,,,,98555,CN120488,,,,,,,,
mondo:0020148,syndromic aniridia,"['syndrome associated with aniridia', 'syndromic aniridia']",,,98557,CN227798,,,,,,,,
mondo:0020153,cryptophthalmia,['cryptophthalmos'],0111716,,98562,,,C124520,,,743.06,,,
mondo:0020154,microblepharon-ablephara syndrome,,,,98563,CN237783,,,,,,,,
mondo:0020155,eyelid border anomaly,,,,98564,,,,,,,,,
mondo:0020156,syndromic ankyloblepharon,,,,98565,CN227801,,,,,,,,
mondo:0020157,syndromic palpebral coloboma,,,,98566,CN227802,,,,,,,,
mondo:0020158,eyelids malposition disorder,,,,98567,CN227803,,,,,,,,
mondo:0020159,congenital entropion,,,,98568,,,,,,,,10014923,
mondo:0020160,secondary entropion,,,,98569,,,,,,,,,
mondo:0020161,congenital ectropion,,,,98570,,,,,,,Q10.1,,
mondo:0020162,secondary ectropion,,,,98571,,,,,,,,,
mondo:0020163,canthal anomaly,,,,98572,,,,,,,,,
mondo:0020164,epicanthal fold,,,,98573,,,,,,,,,
mondo:0020165,syndromic epicanthus,,,,98574,CN227805,,,,,,,,
mondo:0020167,malposition of external canthus,,,,98576,,,,,,,,,
mondo:0020172,palpebral epidermal tumor,"['neoplasm of skin of eyelid', 'skin of eyelid tumor', 'skin of eyelid neoplasm (disease)', 'tumor of skin of eyelid', 'skin of eyelid tumour', 'tumour of skin of eyelid']",,,98581,CN207033,,,,,,,,
mondo:0020173,benign tumor of palpebral epidermis,['skin of eyelid benign neoplasm'],,,98582,CN207034,,,,,,,,
mondo:0020174,precancerous lesion of palpebral epidermis,['skin of eyelid precancerous condition'],,,98583,,,,,,,,,
mondo:0020175,malignant tumor of palpebral epidermis,"['malignant neoplasm of skin of eyelid', 'skin of eyelid cancer', 'malignant skin of eyelid neoplasm', 'cancer of skin of eyelid']",,,98584,CN207035,,,,,,,,
mondo:0020176,palpebral sebaceous gland tumor,"['neoplasm of sebaceous gland of eyelid', 'tumor of sebaceous gland of eyelid', 'sebaceous gland of eyelid tumor', 'sebaceous gland of eyelid tumour', 'tumour of sebaceous gland of eyelid', 'sebaceous gland of eyelid neoplasm (disease)']",,,98585,CN207036,,,,,,,,
mondo:0020177,pigmented palpebral tumor,"['pigmented palpebral neoplasm', 'pigmented eyelid tumour', 'pigmented eyelid tumor']",,,98586,CN207037,,,,,,,,
mondo:0020178,palpebral lentiginosis,['skin of eyelid lentigo'],,,98587,,,,,,,,,
mondo:0020179,palpebral nevus,"['eyelid nevus', 'melanocytic nevus of skin of eyelid', 'nevus of eyelid', 'nevus of the eyelid', 'skin of eyelid melanocytic nevus']",,,98588,C0239460,,C3880,,,,,,
mondo:0020180,palpebral piliary tumor,,,,98590,CN207040,,,,,,,,
mondo:0020181,mesenchymatous palpebral tumor,,,,98591,CN207041,,,,,,,,
mondo:0020183,neurogenic palpebral tumor,,,,98593,CN207043,,,,,,,,
mondo:0020193,secretory apparatus of the lacrimal system anomaly,"['disorder of lacrimal gland', 'lacrimal gland disease', 'disease of lacrimal gland']",,,98603,,,,,,,,,
mondo:0020194,congenital alacrima,,,,98604,,,,,,,,,
mondo:0020195,excretory apparatus of the lacrimal system anomaly,,,,98605,,,,,,,,,
mondo:0020196,anomaly of the secretory and excretory apparatus of the lacrimal system,,,,98608,,,,,,,,,
mondo:0020197,EEC syndrome and related syndrome,['ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome and related disorders'],,,98609,CN207046,,,,,,,,
mondo:0020203,pigmented conjunctival lesion,,,,98615,,,,,,,,,
mondo:0020204,conjunctival tumor,"['tumor of conjunctiva', 'conjunctiva tumour', 'conjunctival neoplasms', 'tumour of conjunctiva', 'conjunctival neoplasm', 'tumour of the conjunctiva', 'conjunctiva neoplasm (disease)', 'neoplasm of the conjunctiva', 'tumor of the conjunctiva', 'conjunctiva tumor', 'conjunctiva neoplasm', 'neoplasm of conjunctiva', 'conjunctival tumor']",,,98616,,,C2961,,,,,,
mondo:0020205,bulbar conjunctival dermoid or conjunctival dermolipoma,,,,98617,,,,,,,,,
mondo:0020210,syndromic hyperopia,"['syndromic hyperopia', 'syndrome associated with hyperopia']",,,98622,CN227820,,,,,,,,
mondo:0020211,syndromic keratoconus,"['syndromic keratoconus (disease)', 'syndrome associated with keratoconus (disease)']",,,98623,CN227821,"['0.0659', '-0.0163', '-0.1442', '0.379', '-0.3457', '0.0469', '0.0628', '0.381', '-0.7246', '-0.3267', '0.2568', '0.02074', '-0.627', '0.5435', '-0.4653', '-0.207', '-0.2595', '0.11316', '0.03873', '-0.6836', '0.04224', '0.4006', '-0.625', '-0.1061', '-0.2231', '0.00318', '0.1459', '0.1382', '0.3184', '0.6294', '0.236', '0.02092', '0.3167', '0.333', '0.3657', '0.4954', '-0.4429', '-0.2808', '0.1417', '-0.557', '0.5454', '0.2566', '-0.3838', '-0.4392', '-0.6685', '-0.04288', '-0.09485', '-0.3052', '0.9624', '0.4465', '-0.1142', '-0.3208', '0.682', '-0.834', '0.415', '0.0016165', '0.01662', '0.11523', '-0.4368', '-0.57', '-0.5254', '-0.224', '0.02011', '0.05463', '-0.05722', '0.2563', '0.4258', '0.571', '-0.327', '0.9893', '-0.841', '0.1771', '-0.4556', '-0.08826', '-0.11334', '-0.06104', '0.10004', '0.572', '0.2952', '-0.1448', '-0.1829', '-0.1832', '-0.7188', '0.705', '0.01196', '-0.3855', '0.2485', '0.2065', '0.3005', '0.6753', '-0.2378', '-0.1866', '0.1175', '0.651', '0.832', '0.03857', '-0.1759', '-0.4204', '-0.4985', '-0.09735']",,,,,,,
mondo:0020212,superficial corneal dystrophy,"['anterior corneal dystrophy', 'corneal epithelium corneal dystrophy (disease)']",,,98625,C2315777,,,,,371.52,,,
mondo:0020213,stromal corneal dystrophy,"['stromal dystrophy', 'substantia propria of cornea corneal dystrophy (disease)', 'corneal stromal dystrophy']",0060442,,98626,C0038457,,,,,371.56,,,
mondo:0020214,posterior corneal dystrophy,,,,98627,CN227822,,,,,371.58,,,
mondo:0020215,syndromic corneal dystrophy,"['syndrome associated with corneal dystrophy (disease)', 'syndromic corneal dystrophy (disease)']",,,98628,CN227823,,,,,,,,
mondo:0020216,secondary dysgenetic glaucoma,['secondary congenital glaucoma'],,,98631,,,,,,,,,
mondo:0020219,corneogoniodysgenesis,,,,98635,,,,,,,,,
mondo:0020235,lens size anomaly,,,,98652,,,,,,,,,
mondo:0020237,lens shape anomaly,,,,98655,,,,,,,,,
mondo:0020238,inherited vitreous-retinal disease,"['genetic vitreoretinal disease', 'genetic vitreous-retinal disease']",,,98657,CN207063,,,,,,,,
mondo:0020240,syndromic retinitis pigmentosa,"['syndromic retinitis pigmentosa', 'syndrome associated with retinitis pigmentosa']",,,98661,CN227834,,,,,,,,
mondo:0020242,hereditary macular dystrophy,['genetic macular dystrophy (disease)'],,,98664,,,C140264,,,,H35.5,,
mondo:0020246,inherited vitreoretinopathy,,,,98668,C1850109,,,,,,,,0007773
mondo:0020247,congenital vitreoretinal dysplasia,,,,98669,,,,,,743.56,,,
mondo:0020248,vitreoretinal degeneration,['degenerative vitreoretinopathy'],,,98670,C0344290,,,,,,H35.5,,0007964
mondo:0020249,hereditary optic neuropathy,,,,98671,,"['-0.02493', '0.157', '0.1066', '-0.008095', '0.00276', '-0.08405', '0.01869', '0.11975', '-0.1481', '-0.0388', '-0.05084', '-0.0767', '-0.0478', '-0.004158', '-0.0813', '-0.1903', '0.03038', '-0.05368', '0.03552', '-0.2834', '0.0642', '-0.0876', '-0.03415', '0.03485', '-0.005657', '-0.0493', '-0.0857', '0.09283', '-0.02745', '-0.0634', '0.0925', '0.02527', '0.1962', '0.04865', '0.01883', '-0.0478', '0.05756', '-0.0662', '-0.01772', '-0.1362', '-0.09796', '-0.12445', '0.0414', '0.049', '-0.01595', '-0.1251', '0.02385', '0.07263', '0.0522', '0.01411', '0.006077', '0.08405', '-0.0215', '-0.009926', '-0.02968', '0.00647', '0.1885', '-0.02005', '-0.1908', '0.02974', '0.01023', '-0.03476', '0.04996', '0.1339', '-0.1581', '0.05576', '0.1134', '0.2642', '-0.07263', '0.1893', '-0.0941', '0.1233', '0.0814', '-0.1148', '0.05255', '0.04517', '0.0727', '0.1114', '-0.0777', '-0.1141', '0.02695', '-0.0694', '-0.04288', '0.2196', '-0.1261', '-0.06073', '0.06012', '0.1292', '0.1674', '0.00837', '0.0809', '0.12494', '0.004864', '0.01768', '0.2837', '0.0481', '0.1254', '-0.01357', '-0.05463', '0.1069']",,,,,,10061323,
mondo:0020250,autosomal dominant optic atrophy,"['ADOA', 'DOA', 'dominant optic atrophy', 'optic atrophy, autosomal dominant']",,,98672,C0338508,,C84577,,D029241,,,,
mondo:0020252,essential strabismus,,,,98682,,,,,,,,,
mondo:0020256,congenital trochlear nerve palsy,"['congenital superior oblique palsy', 'congenital fourth cranial nerve palsy', 'congenital CNIV palsy']",,,98686,,,,,,,,,
mondo:0020257,supranuclear oculomotor palsy,"['supranuclear disorder of eye movement', 'conjugate gaze palsy', 'gaze palsy', 'supranuclear ocular palsy', 'supranuclear eye movement disorder']",,,98687,,,,,,,,,
mondo:0020275,oculocutaneous or ocular albinism,,,,98706,,,,,,,,,
mondo:0020283,uveitis,"['uveitis', 'uvea inflammation', 'uveitis (disease)']",13141,,98715,C0042164,,C26909,1001231,D014605,,,10046851,0000554
mondo:0020284,heart position anomaly,,,,98716,,,,,,,,,
mondo:0020285,transposition of the great arteries and conotruncal cardiac anomaly,,,,98717,,,,,,,,,
mondo:0020286,aortic malformation,,,,98718,,,,,,,,,
mondo:0020287,pulmonary artery or pulmonary branch anomaly,,,,98719,,,,,,,,,
mondo:0020288,atrioventricular valve anomaly,,,,98720,,,,,,,,,
mondo:0020289,congenital tricuspid malformation,,,,98721,,,,,,,,,0001702
mondo:0020290,familial atrioventricular septal defect,"['common AV canal', 'ECD', 'common atrioventricular canal', 'AV septal defect', 'AVCD', 'endocardial cushion defect', 'atrioventricular septal defect', 'atrioventricular canal defect', 'AVSD']",0050651,,98722,,,C101029,,,745.69,,,
mondo:0020291,hypoplastic right heart syndrome,['right hypoplastic heart syndrome'],0070315,,98723,C0344963,,C99053,,,746.89,Q22.6,10064962,
mondo:0020292,congenital anomaly of the great arteries,"['congenital aorta, aortic arch or pulmonary arteries anomaly']",,,98724,,,,,,,,10061080,
mondo:0020293,ascending aorta anomaly,,,,98725,,,,,,,,,
mondo:0020294,atrial defect and interatrial communication,"['atrial defect and interauricular communication', 'rare atrial defect and interatrial communication']",,,98727,,,,,,,,,
mondo:0020295,congenital pulmonary veins anomaly,,,,98729,,,C110942,,,,,,
mondo:0020296,congenital arteriovenous fistula,,,,98731,,,C35377,,D001164,,,10003226,
mondo:0020297,Noonan syndrome and Noonan-related syndrome,,,,98733,CN166718,,,,C537846,,,,
mondo:0020298,Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15,"['Prader-Willi syndrome due to maternal uniparental disomy of chromosome type 15', 'UPD(15)mat']",,,98754,CN207093,,,,,,,,
mondo:0020300,autosomal dominant nocturnal frontal lobe epilepsy,"['ENFL', 'ADNFLE']",0060681,,98784,C3696898,"['0.945', '0.4102', '-0.3943', '-0.2074', '-0.595', '-0.2698', '1.072', '0.2423', '-0.5586', '-0.4148', '-0.2006', '-0.2566', '-0.10266', '0.3357', '0.03793', '0.4927', '-0.459', '-0.6416', '-0.3318', '-0.4824', '-0.1963', '0.3904', '0.1475', '-0.503', '-0.11066', '-0.10846', '-0.1584', '-0.1743', '-0.5146', '0.4736', '0.2925', '-0.552', '0.2668', '0.1268', '0.6494', '0.3528', '-0.03265', '0.04968', '0.10126', '-0.417', '0.069', '-0.5786', '0.1117', '-0.3965', '-0.2969', '-0.6274', '-0.4136', '0.3655', '0.3079', '0.8174', '-0.0264', '0.1239', '-0.03004', '-0.4248', '0.3865', '-0.2156', '-0.1886', '0.1636', '-0.19', '0.3096', '-0.723', '0.4675', '0.7744', '-0.2202', '-0.4377', '1.302', '0.1539', '0.02116', '-0.6934', '0.411', '0.7964', '0.7573', '-0.11444', '-0.2744', '0.4094', '0.755', '0.995', '0.2668', '-0.4177', '0.3123', '-0.1351', '0.65', '0.523', '0.2012', '0.2362', '0.3462', '0.4036', '0.626', '0.6094', '0.448', '-0.04587', '0.03262', '-0.2617', '-0.0639', '0.1125', '0.02113', '0.573', '-0.517', '0.3857', '0.07367']",,,C579932,345.80,,,
mondo:0020301,Prader-Willi syndrome due to paternal 15q11q13 deletion,,,,98793,CN207115,,,,,,,,
mondo:0020302,Angelman syndrome due to maternal 15q11q13 deletion,['Angelman syndrome due to maternal monosomy 15q11q13'],,,98794,CN207116,,,,,,,,
mondo:0020303,Angelman syndrome due to paternal uniparental disomy of chromosome 15,"['Angelman syndrome due to paternal uniparental disomy of chromosome type 15', 'UPD(15)pat']",,,98795,CN207117,,,,,,,,
mondo:0020304,isochromosomy Yp,,,,98797,,,,,,,,,
mondo:0020305,isochromosomy Yq,,,,98798,,,,,,,,,
mondo:0020307,"benign childhood occipital epilepsy, Panayiotopoulos type","['early-onset benign childhood occipital epilepsy', 'Panayiotopoulos syndrome']",,,98815,CN207127,,,,,345.80,,,
mondo:0020308,"benign childhood occipital epilepsy, Gastaut type",['late-onset benign childhood occipital epilepsy'],,,98816,CN207128,,,,,,,,
mondo:0020310,familial focal epilepsy with variable foci,"['epilepsy, familial focal, with variable foci', 'FFEVF', 'familial partial epilepsy with variable foci']",,,98820,CN207131,"['0.8423', '0.1522', '-0.2236', '-0.29', '-0.5337', '-0.395', '0.798', '0.406', '-0.5835', '-0.4707', '0.0777', '-0.188', '-0.182', '0.3767', '0.0945', '0.3', '-0.41', '-0.528', '-0.3574', '-0.4485', '-0.1875', '0.7593', '0.1775', '-0.4553', '-0.02061', '0.011856', '-0.1572', '-0.1633', '-0.671', '0.1757', '0.3535', '-0.685', '0.2537', '0.0955', '0.7446', '0.316', '-0.03888', '-0.1543', '0.1172', '-0.01813', '0.00814', '-0.4204', '-0.0358', '-0.483', '-0.7393', '-0.742', '-0.4236', '0.2079', '0.2186', '0.7803', '0.095', '0.05124', '0.1324', '-0.516', '0.282', '-0.2273', '-0.2227', '0.0824', '-0.10583', '0.2279', '-0.4841', '0.4844', '0.537', '-0.4521', '-0.4954', '1.373', '0.351', '-0.03317', '-0.886', '0.828', '0.863', '1.064', '-0.1573', '-0.222', '0.04025', '0.7437', '0.976', '0.2593', '-0.4426', '0.2369', '-0.2335', '0.719', '0.5967', '0.4607', '0.3804', '0.3562', '0.1427', '0.445', '0.669', '0.1242', '-0.1274', '0.2441', '-0.3977', '-0.05103', '0.1888', '0.07135', '0.607', '-0.668', '0.243', '0.375']",,,C565785,,,,
mondo:0020311,chronic myelomonocytic leukemia,"['CMML', 'chronic myelomonocytic leukemia (CMML)', 'chronic myelomonocytic leukaemia (CMML)', 'chronic myelomonocytic leukemia']",0080188,,98823,C0023480,,C3178,,D015477,,,10009018,
mondo:0020316,acute myeloid leukemia with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22),"['acute myelomonocytic leukaemia', 'CBFB-MYH11', 'acute myelomonocytic leukemia', 'AML with inv(16)(p13.1q22) or t(16;16)(p13.1;q22)', 'AML with abnormal bone marrow eosinophils inv(16)(p13q22) or t(16;16)(p13;q22)']",,,98829,C0023479,,,,,,,,
mondo:0020317,acute myeloid leukemia with 11q23 abnormalities,"['acute myeloid leukaemia with t(9;11)(p22;q23); MLLT3-MLL', 'acute myeloid leukemia with t(9;11)(p22;q23); MLLT3-MLL', 'acute myeloid leukaemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A', 'acute myeloid leukemia with MLL abnormalities', 'AML with 11q23 abnormalities', 'acute myeloid leukemia with t(9;11)(p22.3;q23.3); MLLT3-KMT2A', 'acute myeloid leukaemia with MLL abnormalities', 'acute myeloid leukemia with 11q23 (MLL) abnormalities', 'AML with t(9;11)(p22;q23); MLLT3-MLL', 'acute myeloid leukaemia with 11q23 (MLL) abnormalities', 'acute myeloid Leukaemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A', 'acute myeloid Leukemia with t(9;11)(p21.3;q23.3); MLLT3-KMT2A']",,,98831,,,C82403,,,,,,
mondo:0020320,acute myeloblastic leukemia with maturation,"['M2 acute myeloblastic leukemia with maturation', 'acute myeloid leukemia with maturation', 'M2 acute myelocytic leukaemia with maturation', 'AM', 'M2 acute granulocytic leukaemia', 'M2 acute myeloid leukaemia', 'acute M2 myeloid leukemia', 'acute myeloid leukaemia (AML-M2)', 'M2 acute myelogenous leukaemia', 'acute myeloblastic leukaemia M2', 'M2 acute myeloblastic leukaemia', 'acute myelogenous leukemia with maturation', 'M2 acute myeloid leukaemia with maturation', 'AML with maturation', 'M2 acute myeloblastic leukaemia with maturation', 'AML M2', 'acute myeloblastic leukemia M2', 'acute M2 myeloid leukaemia', 'M2 acute myeloid leukemia', 'acute myelocytic leukaemia with maturation', 'M2 acute myelocytic leukemia with maturation', 'M2 acute granulocytic leukemia', 'M2 acute myelogenous leukemia', 'acute myeloblastic leukemia type 2', 'M2 acute myeloid leukemia with maturation', 'acute myelogenous leukaemia with maturation', 'FAB M2', 'M2 acute myelogenous leukaemia with maturation', 'acute myeloid leukemia (AML-M2)', 'M2 acute myeloblastic leukemia', 'LAM M2', 'M2 acute myelogenous leukemia with maturation', 'acute myelocytic leukemia with maturation', 'acute myeloblastic leukaemia type 2', 'acute myeloid leukaemia with maturation']",0081087,,98834,,,C3250,0003028,,,,,
mondo:0020321,acute undifferentiated leukemia,"['stem cell acute leukemia', 'AUL', 'stem cell acute leukaemia', 'acute undifferentiated leukemia', 'stem cell leukaemia', 'stem cell leukemia', 'undifferentiated acute leukaemia', 'acute myeloid leukemia, minimal differentiation, FAB M0', 'acute leukaemia not otherwise specified', 'undifferentiated acute leukemia', 'leukaemia stem cell', 'leukemia stem cell']",,,98835,C1282947,,C9298,,,,,10045516,
mondo:0020322,acute biphenotypic leukemia,"['B- and T-cell mixed leukemia', 'B- and T-cell mixed leukaemia']",9953,,98837,C0023464,,C4673,1000828,D015456,207.80,,10067399,
mondo:0020323,primary mediastinal large B-cell lymphoma,"['B-cell diffuse large cell lymphoma of the mediastinum', 'B-cell diffuse large cell lymphoma of mediastinum', 'mediastinal B-cell diffuse large cell lymphoma', 'primary mediastinal clear cell lymphoma of B-cell type', 'primary mediastinal B-cell lymphoma', 'PMLCL', 'large cell lymphoma of the mediastinum', 'mediastinal (thymic) large B-cell lymphoma', 'mediastinal diffuse large cell lymphoma with sclerosis', 'PMBL', 'mediastinal diffuse large-cell lymphoma with sclerosis', 'primary mediastinal large B-cell lymphoma', 'primary mediastinal (thymic) large B-cell lymphoma', 'Med-DLBCL', 'mediastinal large B-cell lymphoma']",0080210,,98838,C1292754,,C9280,,,,,10036710,
mondo:0020324,intravascular large B-cell lymphoma,"['intravascular lymphomatosis', 'intravascular large B-cell lymphoma', 'IVBCL', 'Tappeiner-Pfleger disease', 'angiotropic lymphoma', 'angioendotheliomatosis proliferans systemisata', 'angiotropic large cell lymphoma', 'malignant angioendotheliomatosis', 'intravascular B-cell lymphoma']",0081311,,98839,CN207146,,C4342,,,202.80,,10069643,
mondo:0020325,anaplastic large cell lymphoma,"['anaplastic large cell lymphoma', 'primary systemic ALCL', 'ALCL', 'CD30 Positive anaplastic large cell lymphoma', 'Ki-1+ ALCL', 'Ki-1+ anaplastic large cell lymphoma', 'CD30 positive anaplastic large cell lymphoma', 'Ki-1 lymphoma', 'sACL', 'Ki-1 positive anaplastic large cell lymphoma']",0050744,,98841,C0206180,,C3720,0003032,D017728,200.60,,,
mondo:0020326,lymphomatoid papulosis,"['LyP', 'LYP']",,,98842,C0206182,,C3721,1000341,D017731,447.8,,10056670,
mondo:0020327,"classic Hodgkin lymphoma, nodular sclerosis type",,,,98843,,,,,,,,,
mondo:0020331,indolent systemic mastocytosis,"['indolent systemic mastocytosis (morphologic abnormality)', 'ism']",4660,,98848,C0272203,,C9286,,,,,10056452,
mondo:0020332,systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease,"['systemic mastocytosis with an associated hematological neoplasm (SM-AHN)', 'systemic mastocytosis with associated clonal hematological non-mast-cell lineage disease', 'systemic mastocytosis with associated clonal hematological non-mast cell lineage disease', 'systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease (morphologic abnormality)', 'systemic mastocytosis with associated hematologic neoplasm', 'systemic mastocytosis with an associated haematological neoplasm (SM-AHN)', 'systemic mastocytosis with associated clonal, hematologic non-mast-cell lineage disease', 'systemic mastocytosis with an associated hematological neoplasm', 'SM-AHNMD', 'systemic mastocytosis with associated clonal haematological non-mast cell lineage disease', 'SMAHN', 'systemic mastocytosis with associated clonal haematological non-mast-cell lineage disease', 'systemic mastocytosis with an associated haematological neoplasm', 'SM-AHN']",4797,,98849,,,C9284,1000559,,,,,
mondo:0020333,aggressive systemic mastocytosis,"['lymphadenopathic mastocytosis with eosinophilia', 'ASM', 'aggressive systemic mastocytosis (morphologic abnormality)']",4798,,98850,C1112486,,C9285,,,,,10056453,
mondo:0020334,mast cell leukemia,"['Mast cell leukaemia', 'aleukemic mast cell leukaemia', 'Mast cell leukemia', 'SMMCL', 'mast-cell leukaemia', 'mast-cell leukemia', 'aleukemic mast cell leukemia']",9254,,98851,C0023461,,C3169,0007359,D007946,,,10056450,
mondo:0020336,autosomal dominant Emery-Dreifuss muscular dystrophy,"['EDMD2', 'Emery-Dreifuss muscular dystrophy, autosomal dominant']",,,98853,C0410190,,,,,,,,
mondo:0020337,congenital dyserythropoietic anemia type 1,"['CDA type 1', 'CDA type I', 'congenital dyserythropoietic anemia type 1', 'dyserythropoietic anemia, congenital type 1', 'type I congenital dyserythropoietic anaemia', 'type I congenital dyserythropoietic anemia', 'anemia, dyserythropoietic, congenital type 1', 'CDA I']",0111396,,98869,,"['-0.3528', '0.1819', '-0.1326', '0.3708', '0.4253', '0.0809', '-0.3774', '0.5522', '0.10944', '-0.656', '0.4675', '0.1501', '0.4724', '0.4453', '-1.306', '-0.05103', '-0.8154', '0.1481', '-0.4033', '-0.4988', '-0.1255', '-0.511', '0.716', '-0.1213', '0.443', '-0.3474', '-0.1071', '-0.1849', '0.4705', '0.1436', '0.07227', '-0.006012', '0.505', '0.67', '0.4482', '-0.553', '-0.4202', '-0.8687', '0.494', '-0.2225', '-0.7266', '0.5386', '0.1396', '-0.3315', '-0.656', '-0.5527', '-0.05573', '0.2423', '0.398', '-0.4824', '0.2976', '0.3896', '0.9155', '-0.1605', '0.5796', '-0.4805', '-0.00968', '-0.02637', '-1.015', '-0.05435', '0.0526', '0.2158', '-0.1445', '-0.1152', '0.09', '0.3599', '0.2695', '0.7305', '-0.5645', '0.71', '1.087', '-0.3184', '-0.548', '-0.5093', '0.556', '1.04', '0.1497', '-0.1567', '-0.0071', '0.1614', '0.2546', '0.0131', '0.03674', '-0.2373', '0.1313', '-0.4343', '-0.509', '0.5347', '0.4465', '-0.2284', '0.3938', '0.2473', '-0.4277', '-0.1445', '0.74', '0.8643', '0.2064', '0.03674', '0.2664', '-0.539']",,,,,,,
mondo:0020338,adult pure red cell aplasia,"['idiopathic pure red cell aplasia', 'pure red-cell aplasia of adults', 'adult pure red-cell aplasia', 'acquired PRCA', 'acquired pure red cell aplasia']",,,98872,C0340961,,C70548,,,,,,
mondo:0020339,X-linked complex spastic paraplegia,"['complicated X-linked HSP', 'Complex X-linked SPG', 'X-linked complicated spastic paraplegia', 'Complex X-linked HSP', 'complicated X-linked SPG']",,,98888,,,,,,,,,
mondo:0020340,bilateral perisylvian polymicrogyria,,0080924,,98889,,"['-0.0794', '0.1516', '0.0874', '-0.08386', '0.1675', '-0.1498', '0.0643', '0.03525', '-0.276', '-0.0615', '-0.1207', '-0.1344', '0.003391', '0.07196', '-0.01109', '-0.06537', '0.05884', '-0.1638', '-0.11285', '-0.2964', '-0.03482', '-0.0709', '0.131', '-0.1125', '0.00964', '-0.0861', '-0.07556', '0.10254', '-0.0127', '0.02486', '0.1302', '-0.04053', '0.2219', '0.0334', '0.1803', '-0.0229', '-0.00998', '0.01874', '-0.01371', '-0.2101', '0.02812', '-0.145', '-0.03308', '-0.0253', '0.06076', '-0.0952', '-0.0231', '0.1984', '-0.03003', '0.0665', '0.03336', '0.002346', '-0.03253', '-0.04443', '-0.1147', '-0.02293', '0.114', '-0.03146', '-0.1299', '0.08105', '0.010056', '-0.02602', '0.1508', '0.11694', '-0.181', '0.05167', '0.2588', '0.1383', '-0.2', '0.1885', '-0.0785', '0.142', '0.1694', '-0.1127', '0.007576', '0.10944', '0.004704', '0.0929', '-0.1185', '-0.1462', '-0.010994', '-0.04968', '0.0897', '0.1738', '-0.05402', '-0.1613', '0.01466', '0.1824', '0.08997', '0.01921', '-0.05057', '0.2201', '0.1224', '0.08014', '0.3162', '0.06885', '0.163', '-0.253', '0.1643', '0.0925']",,,,,,,
mondo:0020341,periventricular nodular heterotopia,['periventricular heterotopia'],0050454,,98892,C1868720,"['0.02933', '0.3262', '0.08203', '-0.3706', '0.2659', '-0.04446', '-0.01692', '0.2913', '-0.2433', '-0.001105', '-0.4246', '-0.2834', '-0.1886', '0.109', '0.2102', '0.001669', '-0.3171', '-0.568', '-0.1729', '-0.0819', '-0.08295', '0.08075', '0.6978', '-0.1417', '-0.2496', '-0.2554', '0.2935', '0.2065', '-0.04053', '0.06525', '0.5527', '-0.2272', '0.3245', '0.1829', '0.2125', '0.2167', '-0.1093', '-0.1536', '0.3616', '-0.3032', '0.2695', '-0.4204', '-0.02975', '-0.2388', '-0.2786', '-0.3547', '0.0989', '-0.1122', '-0.4', '-0.1827', '0.815', '0.2388', '-0.4026', '-0.1454', '-0.411', '0.3481', '0.2018', '-0.2416', '-0.1068', '0.3748', '-0.276', '0.1846', '0.2915', '0.3777', '0.0919', '0.3105', '0.6494', '0.3923', '-0.4136', '0.1863', '0.05316', '0.2461', '0.10297', '0.005207', '-0.376', '0.142', '0.4038', '0.3484', '0.1257', '-0.4763', '-0.65', '0.04224', '-0.1989', '0.502', '-0.0886', '0.03357', '0.1333', '-0.0985', '-0.1554', '0.2896', '0.2866', '0.2805', '-0.00776', '-0.374', '0.633', '-0.0793', '0.775', '-0.519', '0.291', '0.3804']",,,D054091,,,10066854,
mondo:0020343,alpha-crystallinopathy,['CRYAB-related myofobrillar myopathy'],,,98910,,"['0.008026', '-0.001406', '0.009926', '-0.009766', '-0.000774', '-0.002424', '0.004562', '0.004734', '0.002712', '0.005466', '-0.001165', '0.003202', '0.001133', '0.001285', '-0.005627', '0.00562', '-0.008644', '0.00879', '0.007656', '0.00591', '-0.007114', '0.006332', '0.005226', '-0.00786', '0.004784', '-0.01109', '0.0048', '-0.00416', '0.01111', '0.000753', '-0.00511', '0.003084', '0.00847', '0.001097', '-0.001204', '0.001904', '-0.003712', '0.0093', '-0.005146', '0.0003583', '-0.0001875', '0.002886', '-0.00756', '-0.00525', '-0.004406', '0.001519', '0.00746', '-0.001216', '0.00571', '-0.002558', '0.00928', '-0.003422', '-0.001845', '-0.003458', '0.0002228', '-0.011284', '0.007515', '-0.00559', '-0.00508', '0.00901', '0.006897', '-0.00211', '-0.0085', '-0.0009108', '-0.006413', '-0.00743', '-0.002266', '-0.002926', '-0.007935', '0.002565', '0.005226', '-0.005383', '0.003311', '-0.01564', '-0.007286', '0.00882', '0.002768', '0.000855', '0.006664', '-0.00892', '0.007427', '-0.00507', '0.001459', '0.01417', '-0.00872', '-0.01058', '0.002663', '0.01091', '0.0002196', '-0.005947', '-0.002516', '0.005665', '-0.007', '-0.00781', '0.007454', '0.00685', '0.01061', '-0.00854', '-0.011284', '-0.004345']",,,,,,,
mondo:0020344,postsynaptic congenital myasthenic syndrome,['postsynaptic congenital myasthenic syndromes'],,,98913,,"['-0.05838', '0.07837', '0.00505', '0.02225', '0.04315', '-0.0779', '0.01938', '0.03842', '-0.05637', '-0.1044', '0.01227', '-0.04706', '0.015526', '0.07623', '-0.05365', '-0.005817', '-0.04657', '-0.05615', '-0.01875', '-0.2246', '0.00638', '0.01301', '0.11017', '-0.0508', '0.02022', '-0.00829', '-0.04004', '-0.08636', '0.04813', '-0.09717', '0.09357', '0.07385', '0.1142', '0.0422', '-0.002474', '-0.01985', '-0.02266', '-0.03745', '-0.0674', '-0.0848', '0.0736', '-0.10583', '-0.00946', '-0.03296', '0.05408', '-0.1107', '-0.02486', '0.0865', '0.0713', '0.05542', '-0.05762', '-0.00519', '0.01784', '-0.01636', '-0.07947', '-0.04437', '0.0832', '0.00931', '-0.09314', '0.03165', '0.06537', '-0.01665', '0.01388', '0.0198', '-0.003187', '0.01168', '0.07465', '0.06854', '-0.1268', '0.1666', '-0.0755', '0.02568', '0.04276', '-0.03056', '0.0979', '0.06174', '0.013504', '-0.004086', '-0.0966', '-0.05783', '-0.014656', '0.01712', '-0.0189', '0.06323', '0.00484', '-0.0507', '0.06586', '0.09753', '0.0939', '0.03555', '0.0963', '0.0834', '0.05246', '0.04697', '0.14', '0.07446', '0.1104', '-0.1362', '-0.02376', '0.02832']",,,,,,,
mondo:0020345,presynaptic congenital myasthenic syndrome,['presynaptic congenital myasthenic syndromes'],,,98914,,"['-0.04825', '0.0886', '-0.02715', '0.01067', '0.0347', '-0.088', '0.02243', '0.07385', '-0.0663', '-0.09576', '-0.01178', '-0.0473', '0.001082', '0.04517', '-0.0324', '-0.01451', '-0.03186', '-0.036', '-0.01868', '-0.2231', '0.01466', '0.0187', '0.10956', '-0.03723', '0.02245', '0.004948', '-0.05118', '-0.08136', '0.04022', '-0.083', '0.1113', '0.0701', '0.11475', '0.04987', '-0.006016', '-0.02069', '0.001557', '-0.02446', '-0.0707', '-0.0772', '0.06274', '-0.1059', '-0.00791', '-0.0335', '0.0406', '-0.111', '-0.02792', '0.0965', '0.05118', '0.0417', '-0.05862', '-0.0268', '0.02522', '-0.0001252', '-0.0831', '-0.05896', '0.09247', '0.01685', '-0.0644', '0.02907', '0.0783', '-0.00544', '0.007355', '0.03366', '-0.008514', '-0.006577', '0.0677', '0.0974', '-0.1203', '0.1526', '-0.10114', '0.04126', '0.03873', '-0.01906', '0.07544', '0.0268', '0.007496', '-0.03497', '-0.0858', '-0.05045', '-0.04825', '0.01512', '-0.0181', '0.0652', '0.00465', '-0.0562', '0.05814', '0.0923', '0.08417', '0.02493', '0.09546', '0.0891', '0.0522', '0.02805', '0.1417', '0.0715', '0.1073', '-0.1175', '-0.01348', '0.03047']",,,,,,,
mondo:0020346,synaptic congenital myasthenic syndrome,['synaptic congenital myasthenic syndromes'],,,98915,,"['-0.088', '0.1003', '0.01205', '-0.01245', '0.0485', '-0.0816', '-0.012085', '0.0634', '-0.05005', '-0.0978', '-0.03973', '-0.05414', '0.010086', '0.02974', '-0.05957', '0.00951', '-0.01767', '-0.0642', '-0.03317', '-0.2379', '0.02751', '0.0083', '0.1371', '-0.04263', '0.03073', '0.003439', '-0.04422', '-0.0837', '0.05487', '-0.10626', '0.107', '0.08765', '0.1204', '0.0671', '0.00522', '-0.03607', '-0.0147', '-0.01439', '-0.0885', '-0.0952', '0.0668', '-0.10364', '-0.0032', '-0.02258', '0.0215', '-0.1702', '-0.011986', '0.0939', '0.0613', '0.0372', '-0.05872', '0.00518', '0.01788', '0.01648', '-0.1179', '-0.05963', '0.10516', '0.004955', '-0.1112', '0.04636', '0.09125', '-0.02058', '-0.01569', '0.06104', '-0.01088', '-0.0215', '0.098', '0.099', '-0.1252', '0.1755', '-0.11993', '0.0341', '0.02481', '-0.0254', '0.0714', '0.02303', '0.01685', '-0.01704', '-0.1085', '-0.07227', '0.007587', '0.0066', '-0.003443', '0.0626', '-0.011', '-0.04218', '0.05252', '0.12054', '0.0647', '0.0185', '0.0973', '0.10864', '0.0593', '0.03162', '0.1652', '0.07104', '0.1537', '-0.1554', '0.00958', '0.03806']",,,,,,,
mondo:0020347,acute inflammatory demyelinating polyradiculoneuropathy,"['GBS, acute inflammatory demyelinating polyradiculoneuropathic form', 'acute idiopathic demyelinating polyneuropathy', 'Guillain-Barre syndrome, acute inflammatory demyelinating polyradiculoneuropathic form', 'acute inflammatory demyelinating polyradiculopathy', 'AIDP', 'Guillain-Barré syndrome, acute inflammatory demyelinating polyradiculoneuropathic form', 'acute inflammatory polyneuropathy']",,,98916,CN207194,,C116926,,,,,,
mondo:0020348,acute motor and sensory axonal neuropathy,"['AMSAN', 'acute motor-sensory axonal Guillain-BarrC) syndrome', 'acute motor-sensory axonal neuropathy', 'acute motor-sensory axonal GBS', 'acute motor-sensory axonal Guillain-Barré syndrome']",,,98917,CN207195,,C116927,,,,,,
mondo:0020349,acute motor axonal neuropathy,"['acute pure motor Guillain-Barre syndrome', 'acute pure motor GBS', 'acute pure motor Guillain-Barré syndrome', 'AMAN']",,,98918,CN207196,,C116929,,,,,,
mondo:0020351,Blake pouch cyst,,,,98922,,,,,,,,,
mondo:0020352,"multiple system atrophy, parkinsonian type","['MSA, parkinsonian type', 'MSA-p']",,,98933,CN207200,,,,,,G23.2,,
mondo:0020353,von Hippel anomaly,,,,98941,,,,,,,,,
mondo:0020354,coloboma of choroid and retina,"['choroidal coloboma', 'retinochoroidal coloboma', 'retinal coloboma']",,,98942,,"['-0.255', '-0.1621', '-0.01833', '-0.05096', '0.1888', '-0.06033', '0.01146', '0.2025', '-0.1368', '-0.241', '-0.2344', '-0.4087', '-0.1769', '-0.1021', '-0.502', '-0.2208', '0.3328', '-0.1396', '0.10846', '-0.658', '-0.184', '-0.01744', '0.1989', '0.199', '-0.05807', '0.0963', '-0.198', '0.03683', '0.0859', '0.3665', '0.4526', '-0.1918', '0.18', '0.1348', '0.0457', '0.2935', '0.2054', '-0.1813', '-0.006363', '-0.4001', '0.4004', '0.0449', '0.0423', '-0.10535', '-0.1538', '-0.05023', '0.253', '-0.007187', '0.0727', '0.0927', '0.0561', '-0.06866', '-0.0776', '-0.38', '-0.2905', '-0.0629', '0.533', '-0.02737', '-0.584', '0.0689', '0.1406', '0.002647', '0.1893', '0.2905', '-0.2422', '0.0935', '0.5522', '0.5117', '-0.135', '0.623', '-0.0541', '0.212', '-0.01558', '-0.085', '0.06903', '-0.1896', '0.243', '-0.1654', '-0.1703', '-0.1415', '0.005795', '0.01666', '0.3132', '0.63', '-0.4033', '-0.508', '-0.002962', '0.265', '0.3074', '0.177', '0.2742', '0.5186', '0.1425', '0.0902', '0.6704', '-0.3206', '0.3342', '-0.2008', '-0.137', '0.167']",,,,,,,
mondo:0020355,coloboma of eye lens,,,,98943,,,,,,,,,
mondo:0020356,coloboma of iris,"['coloboma of the iris', 'coloboma of iris (disease)', 'coloboma of iris']",,,98944,,"['-0.4727', '0.05847', '0.3508', '-0.1915', '0.2747', '0.0839', '0.211', '-0.07404', '-0.2122', '-0.2283', '-0.2139', '-0.365', '-0.01886', '0.1323', '-0.536', '-0.3245', '0.1577', '-0.4202', '0.3743', '-0.5806', '-0.10504', '-0.002457', '0.3572', '-0.09064', '0.1505', '0.06537', '-0.2698', '0.0977', '0.2074', '0.3137', '0.524', '0.0664', '0.2323', '0.1256', '0.1866', '0.04532', '0.1564', '0.06183', '-0.1534', '-0.6963', '0.1824', '0.01014', '-0.1448', '-0.23', '0.00391', '-0.249', '0.0843', '0.10583', '0.3306', '0.298', '-0.03183', '0.03738', '-0.0916', '-0.3008', '-0.3726', '-0.2208', '0.3726', '0.005054', '-0.6147', '-0.1131', '0.1317', '-0.10925', '-0.03198', '0.655', '-0.2788', '-0.1481', '0.685', '0.2217', '0.05225', '0.2163', '-0.0985', '0.1095', '0.1973', '0.0724', '-0.2186', '0.1992', '0.2332', '0.2627', '-0.3376', '-0.3347', '0.03099', '-0.1238', '0.4016', '0.4934', '-0.1274', '-0.754', '0.1077', '0.4048', '-0.03156', '0.0495', '0.2123', '0.4568', '0.295', '-0.02097', '0.759', '-0.3518', '0.2917', '-0.2524', '0.007786', '0.3992']",C98879,,,,,10052642,0000612
mondo:0020357,coloboma of eyelid,['coloboma of the eyelid'],,,98946,C0521573,,C98878,,,,,,
mondo:0020359,congenital symblepharon,,0111720,,98948,,,,,,,,,
mondo:0020360,complete cryptophthalmia,,0111719,,98949,,,,,,,,,
mondo:0020361,partial cryptophthalmia,,0111718,,98950,,,,,,,,,
mondo:0020362,inverse Marcus-Gunn phenomenon,,,,98951,CN207213,,,,,,,,
mondo:0020363,honey-droplet corneal dystrophy,,,,98958,CN207218,,,,,,,,
mondo:0020364,posterior polymorphous corneal dystrophy,"['hereditary polymorphus posterior corneal dystrophy', 'corneal dystrophy, posterior polymorphous', 'PPCD', 'Schlichting dystrophy', 'posterior polymorphous dystrophy']",0060457,,98973,CN239252,"['-0.5654', '-0.376', '-0.4243', '-0.00294', '0.0687', '-0.46', '-0.0701', '0.4062', '-0.6294', '-0.262', '0.2527', '-0.2197', '-0.4077', '0.08014', '-0.2363', '-0.098', '0.2385', '-0.8604', '0.6797', '-0.9424', '-0.1765', '-0.0318', '0.3796', '0.8525', '-0.006702', '-0.1642', '-0.6323', '0.2247', '-0.3564', '0.4565', '0.4167', '0.2522', '0.04175', '0.5273', '-0.0511', '0.2314', '0.1656', '0.1816', '1.041', '-0.379', '0.7583', '-0.866', '0.4573', '-0.03625', '-0.364', '0.2195', '-0.2317', '0.1219', '0.3342', '0.1766', '0.5903', '-0.1428', '0.3657', '-0.1064', '-0.739', '0.462', '0.3752', '-0.3694', '-0.8457', '0.308', '-0.147', '-0.1766', '-0.2452', '-0.05328', '0.06052', '-0.06665', '0.5884', '0.6323', '-0.2037', '0.649', '0.05725', '-0.2494', '0.4053', '0.2793', '0.5376', '-0.0973', '0.441', '0.025', '-0.1792', '0.06714', '-0.2969', '-0.4697', '-0.4602', '0.3416', '-0.3184', '-0.504', '-0.372', '-0.1103', '0.2937', '0.11194', '0.5415', '0.3403', '0.484', '0.3657', '0.594', '-0.1175', '0.0667', '-0.6943', '-0.0848', '0.307']",,,,,,,
mondo:0020365,congenital hereditary endothelial dystrophy type I,"['congenital hereditary endothelial dystrophy type 1', 'CHED1', 'autosomal dominant CHED', 'CHEDI', 'autosomal dominant congenital hereditary endothelial dystrophy']",,121700,98975,,,,,,,,,
mondo:0020366,congenital glaucoma,"['primary congenital glaucoma', 'buphthalmia', 'buphthalmos', 'Buphthalmus']",,,,,,C50648,,,,,,
mondo:0020367,juvenile open angle glaucoma,"['pediatric glaucoma (disease)', 'glaucoma (disease) of childhood', 'JOAG', 'glaucoma of childhood', 'paediatric glaucoma (disease)']",1068,,98977,C2981140,,,,,365.14,,10064032,
mondo:0020368,Axenfeld anomaly,,,,98978,,,,,,743.44,,10058653,
mondo:0020369,Chandler syndrome,"['dystrophy of corneal endothelium', 'Chandler^s syndrome', 'posterior membrane corneal dystrophy', 'endothelial corneal dystrophy']",11554,,98979,C0544008,,,,,371.57,,10057487,
mondo:0020370,Cogan-Reese syndrome,,0060217,,98980,C1168173,,C84644,,,,,10059200,
mondo:0020371,essential iris atrophy,,,,98981,CN207238,,,,,364.51,,,
mondo:0020372,early-onset sutural cataract,['early-onset cataract with Y-shaped suture opacities'],,,98985,,,,,,,,,
mondo:0020373,early-onset anterior polar cataract,"['cataract anterior polar', 'early-onset anterior subcapsular cataract']",,,98988,C1855179,,,,,,,,
mondo:0020374,cerulean cataract,"['cataract, congenital, blue dot type 1', 'blue-dot cataract', 'cataract, congenital, cerulean type 1']",,,98989,,,,,C537955,743.39,,,
mondo:0020375,coralliform cataract,,,,98990,CN207246,,,,,,,,
mondo:0020376,early-onset nuclear cataract,,,,98991,CN207247,,,,C563333,,,10057735,
mondo:0020377,early-onset partial cataract,,,,98992,CN207248,,,,,,,,
mondo:0020378,early-onset posterior polar cataract,,,,98993,,,,,,,,,
mondo:0020379,early-onset zonular cataract,,,,98995,CN207251,,,,C535342,,,,
mondo:0020380,autosomal dominant cerebellar ataxia,"['ADCA', 'Pierre Marie cerebellar ataxia (formerly)', 'spinocerebellar ataxia', 'SCA', 'autosomal dominant spinocerebellar ataxia', 'cerebellar ataxia, autosomal dominant']",1441,,99,CN227858,"['-0.2507', '-0.283', '0.1371', '0.01723', '-0.2598', '-0.943', '0.010284', '0.06116', '-0.489', '-0.871', '-0.0964', '0.1843', '-0.1738', '-0.0356', '0.536', '-0.258', '-0.0941', '-0.5586', '-0.00408', '-0.7935', '-0.2695', '-0.2252', '0.1395', '-0.399', '0.268', '-0.39', '-0.2825', '0.2922', '0.02449', '-0.5405', '0.06525', '0.4568', '-0.4385', '0.07294', '0.4048', '-0.05478', '0.04922', '0.136', '0.51', '0.4072', '0.512', '0.1663', '-0.4155', '0.3818', '0.49', '-0.598', '0.0345', '0.3586', '0.1765', '-0.09607', '-0.132', '0.274', '-0.2778', '-0.4568', '0.1404', '-0.761', '0.259', '0.2847', '-0.0585', '0.3972', '-0.7837', '0.297', '0.403', '-0.1364', '-0.639', '0.3992', '0.3242', '0.5474', '-0.516', '0.501', '0.6157', '0.4382', '-0.1954', '-0.564', '0.614', '0.402', '0.3992', '0.226', '0.03336', '0.503', '-0.3467', '-0.767', '0.664', '0.613', '-0.562', '-0.6777', '0.322', '0.2362', '0.559', '0.5127', '0.5767', '0.3132', '0.2322', '-0.2468', '0.905', '0.9463', '0.3496', '0.4985', '-0.3574', '0.1781']",,,,334.3,,,
mondo:0020381,patterned macular dystrophy,"['macular dystrophy, patterned', 'patterned dystrophy of retinal pigment epithelium']",0060863,,99001,CN207254,"['-0.0884', '0.03317', '0.02147', '-0.02856', '0.0708', '-0.0812', '-0.03036', '0.05838', '-0.0899', '-0.01439', '-0.02303', '-0.03534', '-0.0671', '0.01212', '-0.04904', '-0.0476', '0.06964', '-0.0573', '-0.001299', '-0.1675', '-0.0527', '-0.066', '0.00623', '0.0257', '-0.02995', '-0.03763', '0.02432', '-0.0174', '-0.04968', '0.007755', '0.0901', '-0.04733', '0.0669', '0.010735', '0.03372', '0.04218', '-0.01298', '0.006725', '0.00814', '-0.1472', '0.05444', '-0.1296', '-0.011154', '-0.0251', '-0.0779', '-0.01488', '0.0006046', '0.0722', '0.01505', '0.0281', '-0.011375', '-0.01874', '0.0724', '0.03256', '-0.03223', '-0.04745', '0.08234', '-0.04593', '-0.1718', '-0.09595', '0.0629', '0.02333', '-0.03583', '0.06183', '0.01268', '0.0085', '0.1757', '0.148', '-0.0898', '0.0781', '-0.0965', '-0.02371', '0.0469', '-0.0387', '0.0325', '0.02757', '0.01243', '-0.03235', '-0.0326', '-0.06052', '0.08124', '-0.05396', '-0.0792', '0.09015', '-0.04776', '-0.01163', '0.011406', '0.1367', '0.1172', '0.0506', '0.013', '0.0842', '0.05154', '0.06805', '0.2181', '0.0069', '0.0415', '-0.1101', '-0.0359', '0.0504']",,,,,H35.5,,
mondo:0020382,multifocal pattern dystrophy simulating fundus flavimaculatus,['multifocal pattern dystrophy simulating Stargardt disease'],,,99003,CN207256,,,,,,H35.5,,
mondo:0020383,fundus pulverulentus,,,,99004,CN207257,,,,,,H35.5,,
mondo:0020384,Niemann-Pick disease type E,,,,99022,,,,,,,,,
mondo:0020385,congenitally uncorrected transposition of the great arteries with coarctation,"['congenitally uncorrected transposition of the great vessels with coarctation', 'TGA with coarctation']",,,99042,,,,,,,,,
mondo:0020386,double outlet right ventricle with subaortic or doubly committed ventricular septal defect with pulmonary stenosis,"['double outlet right ventricle, Fallot type', 'DORV with subaortic or doubly committed VSD with pulmonary stenosis', 'DORV, Fallot type']",,,99043,,,,,,,Q21.3,,
mondo:0020387,double outlet right ventricle with subpulmonary ventricular septal defect,"['Taussig-Bing syndrome', 'DORV-TGA', 'DORV with subpulmonary VSD', 'Double outlet right ventricle with transposition of the great arteries']",,,99045,CN207267,,,,,,,,
mondo:0020388,double outlet right ventricle with non-committed subpulmonary ventricular septal defect,['DORV with non-committed subpulmonary VSD'],,,99046,,,,,,,,,
mondo:0020389,pulmonary valve agenesis-ventricular septal defect-persistent ductus arteriosus syndrome,"['PVA/PDA, non-Fallot type', 'pulmonary valve agenesis-intact ventricular septum-persistent ductus arteriosus syndrome', 'APV/PDA, non-Fallot type', 'absence of pulmonary valve-ventricular septal defect-persistent ductus arteriosus syndrome']",,,99048,CN207270,,,,,,,,
mondo:0020390,pulmonary artery coming from patent ductus arteriosus,,,,99049,,,,,,,,,
mondo:0020391,pulmonary artery coming from the aorta,"['abnormal origin of right or left pulmonary artery from the aorta', 'hemitruncus arteriosus']",,,99050,,,,,,,,,
mondo:0020392,discrete fixed membranous subaortic stenosis,,,,99051,,,,,,,,,
mondo:0020393,discrete fibromuscular subaortic stenosis,,,,99052,,,,,,,,,
mondo:0020394,tunnel subaortic stenosis,,,,99053,,,,,,,,,
mondo:0020395,valvar pulmonary stenosis,,,,99054,,,,,D011666,746.02,,10037450,
mondo:0020396,anomaly of the tricuspid valve chordae,,,,99055,,,,,,,,,
mondo:0020397,parachute tricuspid valve,,,,99056,,,,,,,,,
mondo:0020398,congenital mitral stenosis,"['congenital mitral stenosis (disease)', 'hereditary mitral valve stenosis', 'congenital mitral stenosis']",,,99057,,,,,,746.5,Q23.2,,0011570
mondo:0020399,congenital hypoplasia of the mitral valve annulus,,,,99058,C3165203,,,,,746.89,Q23.2,,
mondo:0020400,congenital supravalvular mitral ring,,,,99059,,,,,,,Q23.2,,
mondo:0020401,congenital unguarded mitral orifice,,,,99060,,,,,,,,,
mondo:0020402,congenital accessory mitral valve tissue,,,,99061,,,,,,,,,
mondo:0020403,congenital mitral valve agenesis,,,,99062,,,,,,,,,
mondo:0020404,shone complex,"['shone^s syndrome (greater than 3 sites)', 'shone syndrome']",,,99063,C1868705,,C99058,,,746.84,,10066802,
mondo:0020405,straddling and/or overriding mitral valve,,,,99064,,,,,,,,,
mondo:0020406,complete atrioventricular canal-left heart obstruction syndrome,"['CAVC-left heart obstruction syndrome', 'CAVC type A', 'complete atrioventricular canal type A']",,,99066,CN207278,,,,,,,,
mondo:0020407,complete atrioventricular canal-ventricle hypoplasia syndrome,"['CAVC type B', 'complete atrioventricular canal type B', 'CAVC-ventricle hypoplasia syndrome']",,,99067,CN207279,,,,,,,,
mondo:0020408,complete atrioventricular canal-tetralogy of fallot syndrome,"['CAVC type C', 'complete atrioventricular canal type C', 'CAVC-Fallot tetralogy syndrome']",,,99068,CN207280,,,,,,,,
mondo:0020409,univentricular heart with single atrio-ventricular valve,,,,99069,,,,,,,,,
mondo:0020410,aorto-right ventricular tunnel,,,,99070,,,,,,,,,
mondo:0020411,aorto-left ventricular tunnel,,,,99071,,,,,,,,,
mondo:0020412,congenital patent ductus arteriosus aneurysm,,,,99072,,,,,,,,,
mondo:0020413,encircling double aortic arch,,,,99075,,,,,,,,,
mondo:0020414,persistent fifth aortic arch,,,,99076,,,,,,,,,
mondo:0020415,Kommerell diverticulum,,,,99077,,,,,,,,,
mondo:0020416,Neuhauser anomaly,,,,99078,,,,,,,,,
mondo:0020417,right aortic arch,"['right aortic arch (disease)', 'right aortic arch']",,,99081,,,C103917,,,,,10067407,0012020
mondo:0020418,dysphagia lusoria,,,,99082,C0267073,,,,,787.29,,,
mondo:0020419,pulmonary artery hypoplasia,"['pulmonary artery hypoplasia (disease)', 'pulmonary artery hypoplasia']",,,99083,,,,,,,,,0004971
mondo:0020420,pulmonary branch stenosis,"['pulmonary artery stenosis, branch (not PPS)', 'peripheral pulmonary stenosis', 'branch pulmonary artery stenosis']",,,99084,C2062889,,C99144,,,,,,
mondo:0020421,coronary artery intramyocardial course,,,,99085,,,,,,,,,
mondo:0020422,aortopulmonary coronary arterial course,,,,99086,,,,,,,,,
mondo:0020423,stenosis or atrophy of the coronary ostium,"['stenosis or atresia of the coronary ostium', 'coronary ostial stenosis or atresia']",,,99087,,,,,,,,,
mondo:0020424,intramural coronary arterial course,,,,99088,,,,,,,,,
mondo:0020425,abnormal number of coronary ostia,,,,99089,,,,,,,,,
mondo:0020426,malposition of the coronary ostium,,,,99090,,,,,,,,,
mondo:0020427,Laubry-Pezzi syndrome,"['VSD with aortic insufficiency', 'ventricular septal defect with aortic insufficiency']",,,99094,CN207292,,,,,,,,
mondo:0020428,congenital Gerbode defect,"['Gerbode defect', 'left ventricular-to-right atrial communication']",,,99095,,,,,,,,,
mondo:0020429,cor triatriatum dexter,"['cor triatriatum dextrum', 'cor triatriatum dexter', 'cor triatriatum dexter (disease)', 'divided right atrium']",,,99098,,,,,,746.89,,,0011566
mondo:0020430,cor triatriatum sinister,"['cor triatriatum sinistrum', 'divided left atrium']",,,99099,,,,,,746.89,,,
mondo:0020431,juxtaposition of the atrial appendages,['juxtaposition of the atrial auricles'],,,99100,,,,,,,,,
mondo:0020432,ectasia of the right atrial appendage,"['ectasia of the right atrial auricle', 'dilatation of the right atrial appendage', 'dilatation of the right atrial auricle']",,,99101,,,,,,,,,
mondo:0020433,ectasia of the left appendage,"['dilatation of the left auricle', 'ectasia of the left auricle', 'dilatation of the left appendage', 'ectasia of the left atrial appendage', 'dilatation of the left atrial appendage']",,,99102,,,,,,,,,
mondo:0020434,"atrial septal defect, ostium secundum type","['osASD', 'ostium secundum atrial septal defect', 'ASD ostium secundum type', 'ASD, ostium secundum type', 'ostium secundum ASD']",,,99103,,,,,,,,10031303,
mondo:0020435,"atrial septal defect, coronary sinus type","['coronary sinus atrial septal defects', 'unroofed coronary sinus', 'ASD, coronary sinus type', 'ASD coronary sinus', 'atrial septal defect coronary sinus']",,,99104,,,,,,746.89,,,
mondo:0020436,"atrial septal defect, sinus venosus type","['sinus venosus atrial septal defects', 'atrial septal defect sinus venosus', 'sinus venosus ASD', 'ASD, sinus venosus type']",,,99105,,,,,C548009,,,,
mondo:0020437,"atrial septal defect, ostium primum type","['ASD ostium primum type', 'partial atrioventricular septal defect', 'PAVC', 'incomplete atrioventricular canal defect with isolated atrial component', 'ASD, ostium primum type', 'partial atrioventricular canal defect with isolated atrial component', 'primum atrial septal defect', 'incomplete atrioventricular septal defect with isolated atrial component', 'partial atrioventricular septal defect: ostium primum type', 'atrioventricular defect with atrial shunting only', 'atrial septal defect ostium primum', 'ostium primum ASD', 'PAVSD']",,,99106,C0031192,,,,D006344,,,,
mondo:0020438,atrial septal aneurysm,,,,99107,C0521533,,,,,,,,
mondo:0020439,patent foramen ovale,"['ostium secundum type atrial septal defect', 'foramen ovale patent', 'patent foramen ovale (disease)', 'patent foramen ovale', 'atrial septal defect within oval fossa', 'defect, patent or persistent, ostium secundum', 'persistent ostium secundum']",13620,,99108,C0016522,,C34619,,D054092,,,10016982,0001655
mondo:0020440,persistent left superior vena cava connecting to the left-sided atrium,"['persistent left superior caval vein connecting to the left-sided atrium', 'persistent left SVC connecting to the left-sided atrium', 'left superior caval vein persisting to the left-sided atrium']",,,99109,,,,,,,,,
mondo:0020441,right superior vena cava connecting to left-sided atrium,"['right SVC connecting to left-sided atrium', 'right superior caval vein connecting to left-sided atrium']",,,99110,,,,,,,,,
mondo:0020442,left superior vena cava persisting to left-sided atrium,"['left superior caval vein persisting to left-sided atrium', 'left SVC persisting to left-sided atrium']",,,99111,,,,,,747.49,,,
mondo:0020443,absence of innominate vein,['absence of brachiocephalic vein'],,,99112,,,,,,,,,
mondo:0020444,subaortic course of innominate vein,['subaortic course of brachiocephalic vein'],,,99113,,,,,,,,,
mondo:0020445,agenesis of the superior vena cava,"['agenesis of the SVC', 'absence of the superior vena cava', 'agenesis of the superior caval vein', 'absence of the SVC', 'absence of the superior caval vein']",,,99114,,,,,,747.49,,,
mondo:0020446,coronary sinus stenosis,,,,99117,,,,,,,,,
mondo:0020447,coronary sinus atresia,,,,99118,,,,,,,,,
mondo:0020448,right inferior vena cava connecting to left-sided atrium,"['right IVC connecting to left-sided atrium', 'right inferior caval vein connecting to left-sided atrium']",,,99119,,,,,,,,,
mondo:0020449,persistent eustachian valve,,,,99120,,,,,,,,,
mondo:0020450,azygos continuation of the inferior vena cava,"['azygos continuation of the IVC', 'azygos continuation of the inferior caval vein']",,,99121,,,,,,,,,
mondo:0020451,congenital stenosis of the inferior vena cava,"['congenital stenosis of the inferior caval vein', 'congenital stenosis of the IVC']",,,99122,,,,,,747.49,,,
mondo:0020452,inferior vena cava interruption,"['IVC interruption', 'Inferior caval vein interruption']",,,99123,,,,,,747.49,,,
mondo:0020453,congenital partial pulmonary venous return anomaly,"['Partial anomalous pulmonary Venous connection', 'Partial anomalous pulmonary Venous return']",,,99124,,,C99004,,,,,,
mondo:0020454,congenital complete agenesis of pericardium,,,,99129,,,,,,,,,
mondo:0020455,congenital partial agenesis of pericardium,,,,99130,,,,,,,,,
mondo:0020456,pleuro-pericardial cyst,,,,99131,,,,,,,,,
mondo:0020457,6-phosphogluconate dehydrogenase deficiency,,,619199,99135,,,,,,,,,
mondo:0020458,hemolytic anemia due to erythrocyte adenosine deaminase overproduction,"['adenosine deaminase, elevated, hemolytic anemia due to', 'adenosine deaminase, elevated, hemolytic anaemia due to']",,301083,99138,CN207319,,,,C566314,,,,
mondo:0020459,unstable hemoglobin disease,,,,99139,C0272006,,,,,282.7,,,
mondo:0020460,acquired von willebrand syndrome,"['acquired von Willebrand disease (hereditary or acquired)', 'acquired von Willebrand disease', 'acquired von willebrand disease', 'Willebrand disease, acquired', 'AVWS']",0111146,,99147,C0272362,,,,,,,10069495,
mondo:0020461,epiblepharon,,,,99169,,,,,,743.63,,,
mondo:0020462,tarsal kink syndrome,,,,99170,CN207325,,,,,,,,
mondo:0020463,isolated congenital ectropion,['nonsyndromic congenital ectropion'],,,99171,,,,,,,,,
mondo:0020464,euryblepharon,,,,99172,CN207327,,,,,,,,
mondo:0020465,congenital eyelid retraction,,,,99176,,,,,,,,,
mondo:0020466,monosomy X,['monosomy type X'],,,99226,CN776902,,C36630,,,,,,
mondo:0020467,mosaic monosomy X,"['Mosaic Turner syndrome', 'XX/XO', 'Mosaic monosomy type X']",,,99228,CN776903,,,,,,,,
mondo:0020468,paternal uniparental disomy of chromosome 13,"['UPD(13)pat', 'paternal uniparental disomy of chromosome type 13']",,,99324,,,,,,,,,
mondo:0020469,"48,XYYY syndrome","['48,XYYY']",,,99329,CN207331,,,,,,,,
mondo:0020470,"49,XYYYY syndrome",,,,99330,CN207332,,,,,,,,
mondo:0020472,Turner syndrome due to structural X chromosome anomalies,,,,99413,CN207336,,,,,,,,
mondo:0020473,dappled diaphyseal dysplasia,,,,99645,C1300227,,,,,756.59,,,
mondo:0020474,cheirospondyloenchondromatosis,"['generalized enchondromatosis with platyspondyly', 'generalised enchondromatosis with platyspondyly']",,,99647,C4510810,,,,,,,,
mondo:0020475,dermotrichic syndrome,,,,99688,CN207344,,,,,,,,
mondo:0020476,mesial temporal lobe epilepsy with hippocampal sclerosis,['MTLE-HS'],,,99701,,,,,,,,,
mondo:0020477,progeria-associated arthropathy,,,,99706,,,,,,,,,
mondo:0020478,Leber plus disease,['LHON plus disease'],0111754,,99718,CN207347,"['0.0732', '0.509', '0.3235', '-0.146', '-0.4194', '-0.6006', '0.05423', '0.03662', '-0.3152', '0.0767', '0.2053', '-0.006752', '-0.12115', '-0.266', '0.02722', '-0.2224', '-0.582', '-0.2253', '-0.156', '-0.5845', '0.10175', '-0.537', '-0.1478', '-0.02759', '-0.05814', '0.2142', '-0.1925', '-0.236', '-0.1428', '-0.1283', '-0.2896', '0.3425', '0.6187', '-0.04105', '0.2659', '-0.4546', '-0.4377', '-0.2715', '-0.168', '-0.498', '0.2556', '-0.4292', '0.2352', '0.538', '0.5986', '-0.3398', '-0.2114', '0.3694', '0.2094', '-0.1307', '-0.4473', '0.5176', '-0.3164', '-0.3481', '0.2026', '-0.2437', '0.4473', '0.273', '-0.1327', '0.4136', '0.2233', '-0.4243', '0.2937', '0.562', '-0.533', '0.2524', '0.2769', '0.4468', '-0.1079', '0.649', '-0.674', '-0.00978', '0.2095', '0.4924', '-0.03848', '0.3015', '0.2803', '0.4043', '-0.324', '-0.3647', '0.2668', '-0.0864', '-0.169', '0.82', '-0.322', '-0.1187', '0.67', '0.06256', '0.5635', '0.05304', '0.5864', '0.03787', '0.02206', '-0.06964', '0.4292', '0.6934', '0.5312', '0.3914', '0.186', '0.2104']",,,,,H47.2,,
mondo:0020479,pituitary gigantism,"['infantile and juvenile forms of acromegaly', 'gigantism', 'hypophyseal gigantism']",,,99725,,,C93046,,D005877,,,10018265,
mondo:0020480,sulfite oxidase deficiency due to molybdenum cofactor deficiency,"['MOCOD', 'molybdenum cofactor deficiency', 'combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase', 'combined deficiency of sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase']",0111165,,99732,,"['-0.2279', '0.1364', '0.05237', '0.04272', '0.05164', '-0.1422', '0.01773', '0.03152', '-0.02177', '-0.04724', '-0.06088', '-0.0124', '0.004635', '-0.01875', '-0.0002155', '-0.02783', '-0.0559', '-0.01355', '-0.1749', '-0.2925', '-0.003483', '-0.11884', '0.1835', '-0.0276', '-0.04282', '-0.03293', '0.005966', '-0.0482', '-0.006268', '-0.1571', '0.10114', '0.1126', '0.10034', '0.1346', '0.02441', '-0.1918', '0.05307', '-0.02548', '-0.0321', '-0.166', '0.029', '-0.2507', '0.0828', '-0.06027', '-0.1199', '-0.1886', '0.1137', '0.0724', '0.02759', '0.1576', '-0.03125', '-0.1447', '-0.01064', '0.0801', '-0.126', '-0.0434', '0.2241', '-0.1079', '-0.2002', '0.0879', '0.05402', '0.09406', '0.0864', '-0.01688', '0.07117', '0.01854', '0.1891', '-0.01318', '-0.1549', '0.05618', '-0.1128', '-0.0122', '-0.01999', '-0.10486', '0.08496', '0.178', '0.0848', '-0.1034', '-0.1031', '0.01756', '0.02924', '0.02016', '-0.0957', '0.0887', '0.0813', '0.01602', '0.0703', '0.1451', '0.298', '-0.01554', '0.1082', '0.1333', '-0.06235', '-0.08453', '0.2886', '0.1775', '0.10297', '-0.2378', '-0.001802', '0.06']",,,,,,,
mondo:0020481,myotonia fluctuans,"['exercise-induced delayed-onset myotonia', 'MF', 'Fluctuating myotonia']",,,99734,C0752355,"['-0.749', '0.2208', '-0.2471', '-0.3093', '-0.1714', '-0.8296', '0.06207', '0.4463', '-0.5947', '-0.05594', '-0.1711', '0.772', '0.441', '-0.176', '-0.0927', '0.5464', '-0.04544', '-0.6367', '-0.149', '-0.574', '0.0245', '0.2122', '0.0858', '0.1713', '-0.2041', '0.3733', '-0.08777', '-0.2527', '-0.516', '-0.005116', '-0.1692', '0.4492', '-0.1445', '-0.00833', '-0.405', '0.1', '-0.2479', '-0.2915', '0.1627', '0.1181', '0.2766', '-0.4153', '0.57', '0.2399', '-0.02182', '0.2231', '-0.3257', '0.784', '0.714', '0.729', '-0.2094', '-0.1661', '0.2363', '-0.01101', '-0.01317', '-0.2062', '0.817', '-0.454', '-0.4045', '-0.0958', '0.286', '0.438', '0.1694', '-0.1313', '0.00983', '0.1395', '0.06247', '0.05765', '-0.1875', '0.364', '-0.3394', '-0.3215', '0.6055', '-0.1945', '0.8584', '0.79', '-0.05765', '0.383', '0.1288', '-0.1655', '0.639', '-0.356', '0.0647', '-0.2537', '0.2942', '0.488', '-0.03452', '0.3323', '0.5503', '0.08923', '0.2861', '-0.502', '0.4104', '0.3115', '0.515', '0.3357', '0.3215', '-0.873', '-0.279', '-0.1175']",C122789,,,,,,
mondo:0020482,myotonia permanens,,,,99735,CN207354,"['-0.6216', '-0.1146', '-0.086', '-0.541', '-0.4485', '-0.358', '0.533', '0.692', '-0.824', '-0.51', '-0.433', '0.4736', '-0.4795', '0.4297', '0.2191', '0.2537', '-0.10144', '-0.701', '-0.3179', '-0.7183', '0.1333', '-0.183', '0.1991', '0.2101', '-0.2979', '0.369', '0.278', '-0.3096', '0.3057', '-0.3518', '-0.2776', '0.4905', '0.5376', '-0.1587', '-0.2598', '0.0662', '0.0636', '-0.2307', '0.539', '0.0679', '0.2322', '-0.3445', '0.715', '0.5674', '0.006718', '0.3684', '-0.806', '0.2137', '0.6787', '0.576', '-0.1365', '-0.3306', '0.777', '-0.02733', '-0.1209', '0.02048', '0.755', '-0.01686', '0.2222', '-0.02391', '0.2404', '0.252', '-0.2474', '-0.2477', '-0.2546', '-0.1346', '0.518', '0.2295', '-0.1432', '0.3467', '0.1959', '0.2123', '0.4316', '0.3484', '0.4326', '0.672', '-0.0777', '0.1733', '-0.2844', '0.1753', '-0.1431', '0.05084', '0.364', '-0.2169', '0.10394', '0.758', '0.1925', '0.1776', '0.847', '0.4954', '0.2021', '-0.511', '0.0719', '0.2372', '0.3542', '0.2238', '0.4976', '-0.5845', '-0.1895', '-0.0779']",,,,,,,
mondo:0020483,acetazolamide-responsive myotonia,"['ACZ-responsive congenital myotonia', 'myotonia-painful contractions syndrome', 'painful myotonia', 'painful congenital myotonia', 'ACZ-responsive myotonia', 'Acetazolamide-responsive congenital myotonia']",,,99736,,"['-0.5747', '-0.5737', '-0.0539', '-0.3206', '-0.2489', '-0.4463', '0.579', '0.6016', '-0.2957', '-0.4844', '-0.1134', '0.64', '-0.2083', '0.385', '0.0373', '0.4612', '-0.2374', '-0.7637', '-0.2437', '-0.9985', '0.348', '-0.2308', '0.3384', '0.0666', '-0.1624', '0.3562', '0.1006', '-0.4753', '-0.4917', '-0.07904', '0.3093', '0.4248', '-0.1981', '-0.268', '-0.1595', '-0.1923', '-0.1812', '-0.02594', '0.3142', '-0.2737', '0.292', '-0.808', '0.7017', '0.3547', '-0.04117', '-0.0182', '-0.2318', '0.3792', '0.3367', '0.5825', '-0.06216', '-0.156', '0.5986', '-0.05246', '-0.00691', '-0.4963', '1.003', '-0.0633', '-0.253', '0.1692', '-0.0573', '0.2913', '-0.1289', '-0.403', '0.1909', '-0.18', '0.538', '0.04556', '0.04977', '0.5806', '-0.746', '-0.2368', '1.146', '0.1451', '0.995', '0.912', '-0.01499', '-0.0537', '0.209', '-0.1283', '0.06824', '0.05026', '0.783', '-0.3794', '-0.0633', '0.7026', '-0.05887', '0.5127', '0.7515', '0.3713', '0.02235', '-0.1265', '0.3557', '0.02525', '0.1705', '0.1726', '0.1581', '-0.311', '-0.4692', '-0.0648']",,,,,,,
mondo:0020485,King-Denborough syndrome,"['King Denborough syndrome', 'Noonan like contracture myopathy hyperpyrexia', 'Kousseff Nichols syndrome', 'Koussef-Nichols syndrome', 'anesthetic-induced malignant hyperpyrexia in children']",,619542,99741,,,,,C537504,,,,
mondo:0020487,Pontiac fever,,0050150,,99748,C0343528,,C128335,,,041.89,,10054161,
mondo:0020488,atypical progressive supranuclear palsy syndrome,['atypical PSP syndrome'],,,99750,,"['0.288', '1.481', '0.2224', '0.1858', '-0.661', '-0.561', '0.402', '0.4177', '-1.103', '0.566', '0.955', '-0.1589', '-0.302', '0.5625', '0.2087', '-0.0553', '-0.526', '-0.6753', '-0.4146', '-0.4812', '0.1186', '0.3108', '0.04944', '0.2365', '0.2966', '0.2426', '0.2725', '-0.3708', '-0.1714', '1.093', '0.4204', '0.2495', '0.4468', '0.06006', '0.0659', '-0.05432', '0.4011', '0.1455', '0.0895', '-0.761', '1.097', '-0.3809', '-0.2708', '0.3533', '0.612', '-0.2322', '-0.0734', '-0.429', '0.417', '0.6924', '-0.0442', '0.4412', '-0.2428', '-0.923', '0.1504', '-0.811', '-0.1805', '-0.266', '0.09344', '-0.0388', '0.2637', '-0.2954', '-0.718', '-0.262', '-0.2074', '0.5327', '0.3271', '-0.2644', '-0.4434', '0.9287', '-0.697', '0.04156', '-0.06433', '-0.6016', '0.669', '0.573', '-0.1521', '-0.02798', '-0.1887', '0.1084', '0.177', '-1.263', '0.1326', '0.6123', '-0.1305', '-0.466', '0.2712', '-0.09033', '0.6045', '-0.535', '0.632', '0.2598', '-0.51', '0.911', '-0.05698', '1.029', '0.1451', '0.003454', '0.1565', '0.08734']",,,,,,,
mondo:0020489,familial hyperreninemic hypoaldosteronism type 1,"['FHHA1', '18-hydroxylase deficiency', '18-oxidase deficiency', 'CMO II', 'CMO I', 'aldosterone synthase deficiency', 'corticosterone methyloxidase deficiency type I']",,,99763,C4289986,"['-0.4321', '0.2363', '-0.01804', '-0.01137', '0.2278', '-0.1655', '-0.1409', '0.2417', '-0.1927', '-0.11584', '0.01259', '-0.04926', '0.0957', '0.06168', '-0.04968', '-0.02303', '-0.05603', '0.0147', '-0.06067', '-0.3965', '0.04407', '-0.1836', '0.2983', '0.1848', '0.1824', '0.0392', '0.1399', '-0.01985', '0.04468', '-0.1137', '0.1309', '0.199', '0.346', '0.1716', '-0.1637', '-0.3518', '0.05325', '0.03497', '-0.014626', '-0.2727', '-0.0288', '-0.3833', '0.09375', '0.06366', '-0.2131', '-0.3215', '0.02756', '0.1162', '0.2086', '0.1073', '0.0487', '-0.173', '0.06775', '-0.1595', '-0.1833', '-0.1538', '0.3088', '-0.1393', '-0.179', '0.2172', '0.1378', '0.1283', '0.2761', '-0.1128', '0.08405', '0.2192', '0.1846', '0.06604', '-0.2487', '0.014435', '-0.2568', '-0.0519', '0.02022', '-0.00474', '0.2642', '-0.02623', '0.06726', '0.1188', '-0.1047', '0.05588', '0.1287', '0.1509', '-0.003437', '-0.08026', '-0.03394', '0.0917', '0.2358', '0.007275', '0.3323', '-0.01232', '0.02373', '0.09467', '-0.1215', '-0.1615', '0.523', '0.3035', '0.1652', '-0.3384', '-0.2183', '0.2067']",,,,,,,
mondo:0020490,mosaic trisomy 9,"['Mosaic trisomy chromosome 9', 'trisomy 9 mosaicism', 'Mosaic trisomy type 9']",,,99776,CN035918,,,,C535454,,,,
mondo:0020491,subcortical band heterotopia,"['HeCo', 'band heterotopia', 'double cortex syndrome', 'heterotopic cortex', 'Double cortex', 'familial band heterotopia', 'subcortical laminar heterotopia']",0111169,,99796,C4284594,,C116933,,,,,,
mondo:0020492,hemimegalencephaly,"['macrencephaly', 'unilateral megalencephaly']",,,99802,C0431391,,C177779,,D065705,742.4,,,
mondo:0020493,Haddad syndrome,"['ondine-Hirschsprung syndrome', 'congenital central alveolar hypoventilation-Hirschsprung disease syndrome', 'ondine-Hirschsprung disease']",,,99803,,"['-0.1547', '0.6514', '-0.497', '-0.2368', '0.329', '-0.2067', '0.1775', '0.2551', '-0.1284', '-0.3647', '-0.03745', '0.05447', '-0.11554', '0.03574', '-0.2573', '-0.355', '0.07385', '-0.00823', '-0.385', '-0.4004', '-0.1148', '-0.1351', '0.3816', '-0.5337', '-0.2235', '-0.0719', '-0.1682', '-0.1653', '0.2468', '-0.1052', '0.1008', '0.2788', '0.431', '0.2017', '0.1616', '-0.2915', '0.1892', '-0.2563', '-0.4138', '0.2595', '0.0977', '0.2404', '0.07074', '-0.7256', '0.1437', '-0.1445', '-0.0004647', '0.579', '-0.209', '0.4055', '0.0832', '0.4475', '-0.1709', '-0.5713', '-0.3594', '-0.11316', '0.3054', '-0.2325', '-0.5337', '-0.1543', '0.483', '0.2869', '0.4985', '0.1615', '0.1947', '0.1862', '0.3674', '-0.05338', '-0.8867', '0.5776', '-0.573', '-0.05386', '0.2527', '0.09344', '0.1462', '-0.2432', '-0.2367', '0.2284', '-0.473', '-0.2198', '0.1742', '-0.09155', '-0.3242', '0.1649', '0.479', '-0.03047', '0.4814', '0.2358', '-0.0809', '-0.06104', '0.418', '0.0728', '0.4636', '0.2206', '0.2017', '-0.3906', '0.3254', '-0.9346', '0.08344', '0.357']",,,,,G47.3,,
mondo:0020494,oculootodental syndrome,['OOD'],,,99806,C2750325,,,,,,,,
mondo:0020495,PEHO-like syndrome,"['PEHO syndrome-like', 'progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy-like syndrome', 'PEHOL', 'peho-like syndrome']",,617507,99807,,"['-0.509', '-0.1744', '0.11755', '-0.1912', '0.03787', '-0.6343', '-0.006424', '0.5605', '-0.7944', '0.1316', '-0.3342', '-0.479', '0.08527', '-0.4407', '-0.3333', '-0.06793', '0.871', '-0.1173', '-0.3013', '-0.7764', '0.3748', '0.06046', '0.10144', '-0.02563', '0.4883', '-0.02486', '-0.2031', '0.2004', '-0.2075', '-0.00612', '0.35', '0.3025', '0.3538', '0.10046', '0.03152', '0.1366', '0.1996', '0.01203', '-0.2788', '-0.2303', '0.4624', '-0.1826', '-0.06168', '0.0494', '-0.0353', '-0.2769', '-0.3643', '0.3108', '0.0754', '0.304', '-0.581', '0.1034', '-0.1323', '0.1381', '-0.269', '-0.588', '0.09033', '0.08936', '-0.1868', '0.4138', '-0.2642', '-0.0843', '0.01843', '-0.1447', '-0.04706', '-0.0865', '0.3977', '0.3118', '-0.1393', '0.4932', '-0.777', '0.1215', '0.2996', '0.01888', '-0.367', '-0.2683', '0.3433', '-0.0451', '-0.402', '0.2336', '0.1503', '0.0747', '-0.1604', '0.2969', '0.01938', '-0.009735', '-0.01956', '0.441', '0.4092', '0.6104', '-0.0695', '0.2133', '-0.03726', '-0.06125', '0.1866', '0.5', '0.517', '-0.3425', '0.574', '0.2213']",,,,,,,
mondo:0020496,familial porencephaly,"['familial porencephalic white matter disease', 'hereditary porencephaly']",0112313,,99810,,"['-0.00789', '0.1396', '-0.05936', '0.1117', '0.11273', '-0.233', '-0.04266', '0.03583', '-0.1262', '-0.1523', '0.1354', '-0.0631', '0.07544', '-0.12146', '-0.10406', '-0.07184', '-0.0768', '-0.1127', '-0.1019', '-0.4443', '-0.01494', '-0.04507', '0.07007', '-0.0903', '0.10144', '-0.0314', '0.0322', '0.03925', '0.1671', '-0.02116', '0.2332', '0.0057', '0.1971', '-0.0642', '-0.04147', '-0.04227', '0.10455', '-0.0906', '0.11743', '-0.2568', '0.2046', '-0.1637', '0.1134', '-0.1425', '0.02055', '-0.11755', '-0.0722', '0.06274', '0.2035', '0.012726', '-0.0631', '-0.114', '-0.03906', '0.1099', '-0.06494', '-0.215', '0.1666', '0.1201', '-0.411', '0.05908', '0.252', '0.06052', '0.203', '-0.01707', '-0.0878', '0.07477', '0.2869', '0.055', '-0.2446', '0.2002', '-0.3784', '-0.02686', '0.08594', '-0.02382', '0.05902', '0.2822', '-0.0334', '0.0964', '-0.309', '-0.1509', '0.0448', '0.1758', '0.0428', '0.1401', '-0.05463', '-0.04596', '0.1109', '0.132', '0.1503', '0.04434', '0.02975', '0.0941', '0.005512', '0.005478', '0.2947', '0.1389', '0.2517', '-0.3328', '-0.03568', '0.05026']",,,,,,,
mondo:0020497,Turcot syndrome with polyposis,,,,99818,CN207386,,,,,,,,
mondo:0020499,Nipah virus disease,"['Nipah fever', 'Nipah encephalitis']",0050192,,99825,CN207389,,,,,,,,
mondo:0020500,Marburg hemorrhagic fever,"['MHF', 'Green monkey disease', 'Marburg virus disease', 'Marburg disease']",4327,,99826,C0024788,,C84883,0007358,D008379,078.89,,10026822,
mondo:0020501,Crimean-Congo hemorrhagic fever,"['Crimean hemorrhagic fever', 'CCHF', 'Congo-Crimean hemorrhagic fever', 'CHF Congo virus', 'Congo hemorrhagic fever', 'Crimean-Congo haemorrhagic fever', 'Crimean hemorrhagic fever [CHF Congo virus]', 'Congo fever']",12287,,99827,C1304456,,C34682,,D006479,065.0,A98.0,,
mondo:0020502,yellow fever,"['Yellow fever, sylvan', 'jungle yellow fever', 'bronze John', 'urban yellow fever', 'Yellow fever Virus infection', 'sylvatic yellow fever', 'Yellow Jack', 'Yellow fever virus caused disease or disorder', 'YF']",9682,,99829,C0043398,,C35547,,D015004,060.9,,10048240,
mondo:0020504,hereditary recurrent myoglobinuria,['genetic recurrent myoglobinuria'],,,99845,,"['-0.3513', '-0.2617', '-0.1387', '-0.1981', '-0.3264', '-0.0948', '0.1222', '0.5503', '-0.0361', '0.1094', '-0.1606', '0.0605', '-0.1475', '-0.04257', '-0.08777', '0.2969', '-0.009224', '-0.0109', '-0.2065', '-0.921', '0.346', '-0.2025', '0.1149', '-0.1388', '-0.1901', '0.01712', '0.2712', '-0.0825', '-0.268', '-0.10474', '0.1594', '0.3196', '0.2783', '-0.0325', '-0.2554', '0.05774', '-0.1866', '-0.02946', '0.0859', '-0.1098', '0.00822', '-0.4458', '0.252', '0.1381', '-0.3494', '0.074', '-0.01721', '-0.0345', '0.0635', '0.5884', '-0.4238', '-0.0693', '0.1545', '0.0797', '0.05862', '-0.10205', '0.4153', '-0.3953', '0.02705', '-0.1383', '0.2595', '0.1065', '0.0915', '-0.2734', '-0.2306', '-0.06757', '0.3252', '0.4822', '-0.298', '0.234', '-0.221', '0.0705', '-0.0734', '0.2096', '0.1035', '0.3503', '0.3684', '0.3416', '-0.06134', '-0.1976', '0.03366', '-0.001396', '0.08484', '-0.304', '0.2223', '0.2522', '0.0386', '0.186', '0.3591', '0.06354', '0.3945', '0.2803', '-0.2152', '-0.285', '0.415', '0.5176', '0.3342', '-0.361', '-0.3777', '0.05325']",,,,,R82.1,,
mondo:0020505,ravine syndrome,"['progressive encephalopathy with severe infantile anorexia', 'Reunion island-anorexia-vomiting which is irrepressible-neurological signs syndrome']",,,99852,CN207401,,,,,,,,
mondo:0020506,ovarioleukodystrophy,,,,99853,C1847967,"['-0.04303', '0.09125', '-0.02254', '0.01008', '0.01913', '-0.1237', '0.006454', '0.1205', '-0.07886', '-0.0573', '-0.04163', '-0.037', '-0.0113', '0.03925', '0.005146', '-0.02405', '-0.0006294', '-0.0115', '-0.0527', '-0.1614', '-0.02792', '-0.0455', '0.02277', '-0.02739', '0.02493', '-0.01031', '-0.07117', '0.00427', '0.03265', '-0.05338', '0.0717', '0.02425', '0.1136', '0.0357', '0.02943', '-0.05804', '-0.001331', '-0.0853', '0.0242', '-0.1151', '0.014725', '-0.07104', '0.01107', '-0.0543', '-0.01666', '-0.07056', '-0.0257', '0.0726', '-0.007732', '0.03088', '-0.02061', '-0.00631', '0.01619', '0.0007567', '-0.0787', '0.00273', '0.05945', '0.000546', '-0.1107', '0.02286', '0.0618', '0.0489', '-0.004223', '0.005634', '-0.0209', '0.02077', '0.0854', '0.06647', '-0.0927', '0.0756', '-0.04752', '0.01154', '-0.0189', '-0.0865', '0.02467', '0.02356', '0.01379', '0.0315', '-0.02258', '-0.0184', '-0.00122', '0.01784', '-0.013626', '0.09564', '-0.00185', '0.0003853', '0.03793', '0.1042', '0.12134', '0.0198', '0.0778', '0.0646', '-0.0317', '0.02422', '0.1692', '0.08984', '0.07355', '-0.12427', '0.00794', '0.04083']",,,,,,,
mondo:0020507,leukoencephalopathy with vanishing white matter 1,"['childhood ataxia with central nervous system hypomyelinization', 'CACH', 'vanishing white matter leukodystrophy', 'Cree leukoencephalopathy']",0070374,603896,99854,,"['-0.03128', '0.03262', '-0.00868', '-0.02716', '-0.0165', '-0.06006', '-0.008385', '0.01823', '-0.0469', '0.010895', '-0.0367', '-0.03622', '-0.0144', '-0.02826', '0.01149', '-0.02899', '-0.004173', '-0.0222', '-0.02466', '-0.06415', '-0.01549', '-0.02669', '0.03065', '-0.03032', '0.004253', '-0.03732', '-0.01268', '0.005077', '0.01205', '-0.03583', '0.01736', '0.01256', '0.03827', '0.01287', '0.04205', '-0.0372', '-0.01778', '-0.04663', '0.00838', '-0.03955', '0.01904', '-0.04587', '0.02312', '-0.02477', '-0.001823', '-0.02272', '-0.00896', '0.03833', '-0.002628', '-0.01709', '-0.00672', '-0.003822', '0.01224', '0.01431', '-0.01388', '-0.01704', '0.0402', '-0.02736', '-0.0391', '0.01784', '0.02196', '0.01796', '0.01526', '-0.0002804', '-0.0125', '-0.00756', '0.0601', '0.0664', '-0.04565', '0.0656', '-0.02986', '-0.000828', '-0.000708', '-0.02295', '0.006737', '0.02489', '0.0369', '0.02177', '0.006596', '-0.002941', '-0.01118', '-0.00608', '-0.011566', '0.0682', '-0.00967', '-0.002636', '0.02765', '0.02702', '0.01103', '-0.012375', '0.05127', '0.04456', '0.0159', '0.01947', '0.08716', '0.04572', '0.06116', '-0.05173', '-0.01804', '0.02724']",,,,,,,
mondo:0020508,primary syringomyelia,['congenital syringomyelia'],,,99856,C1299627,,,,,,,,
mondo:0020509,secondary syringomyelia,,,,99857,,,,,,,,,
mondo:0020510,idiopathic syringomyelia,,,,99858,C4511700,,,,,,,,
mondo:0020511,precursor B-cell acute lymphoblastic leukemia,"['precursor B-cell acute lymphocytic leukaemia', 'acute B-cell lymphocytic leukemia', 'acute B cell lymphocytic leukaemia', 'B-cell precursor type acute leukaemia', 'B-cell precursor type acute leukemia', 'B-cell lymphoblastic leukaemia', 'B-cell acute lymphocytic leukemia', 'B-cell type acute leukemia', 'B cell precursor type acute leukemia', 'B-ALL', 'B-cell acute lymphoblastic leukemia', 'precursor B-cell acute lymphoblastic leukemia/lymphoma', 'precursor B-lymphoblastic leukemia (B-precursor ALL)', 'precursor B-cell acute lymphocytic leukemia', 'B cell acute lymphocytic leukemia', 'precursor B-lymphoblastic leukemia', 'B-cell lymphoblastic leukemia', 'acute B-cell lymphocytic leukaemia', 'B-cell acute lymphocytic leukaemia', 'B-cell acute lymphoblastic leukaemia', 'precursor B-lymphoblastic leukaemia', 'B acute lymphoblastic leukaemia', 'precursor B-cell acute lymphocytic leukemia/lymphoma', 'acute B cell lymphocytic leukemia', 'B cell precursor type acute leukaemia', 'B acute lymphoblastic leukemia', 'B-cell type acute leukaemia', 'precursor B-lymphoblastic leukaemia (B-precursor ALL)', 'B-precursor ALL', 'B cell acute lymphocytic leukaemia']",0080638,,99860,C0006413,,C8644,,,,,,
mondo:0020512,precursor T-cell acute lymphoblastic leukemia,"['precursor T-cell acute lymphocytic leukaemia', 'precursor T-cell acute lymphocytic leukemia/lymphoma', 'T-ALL', 'precursor T-cell acute lymphocytic leukemia', 'precursor T-cell acute lymphoblastic leukemia/lymphoma']",,,99861,,,,,,,,,
mondo:0020513,spermatocytic seminoma,"['testicular spermatocytic seminoma', 'spermatocytic seminoma', 'spermatocytoma']",7891,,99865,C0334517,,C39921,,,,,,
mondo:0020516,thymic neuroendocrine carcinoma,['thymus neuroendocrine carcinoma'],,,99869,CN207412,,C171031,,,,,,
mondo:0020517,eosinophilic granuloma,"['eosinophilic xanthomatous granuloma', 'eosinophilic granuloma', 'Monostotic Langerhans cell histiocytosis', 'chronic and localised Langerhans cell histiocytosis', 'chronic unifocal Langerhans cell histiocytosis', 'chronic and localized Langerhans cell histiocytosis', 'unifocal Langerhans cell histiocytosis']",,,99871,C0014461,,C3016,,D004803,277.89,,10014956,
mondo:0020518,Hashimoto-Pritzker syndrome,"['Hashimoto-Pritzker disease', 'congenital Langerhans cell histiocytosis', 'Hashimoto-Pritzker histiocytosis']",,,99872,C1275336,,,,C535843,277.89,,,
mondo:0020519,hand-Schuller-Christian disease,"['classic multifocal Langerhans cell histiocytosis', 'hand-Schuller-Christian disease', 'chronic multifocal Langerhans cell histiocytosis', 'multifocal eosinophilic granuloma', 'hand-SChüller-Christian disease', 'multifocal Unisystem Langerhans cell histiocytosis']",,,99873,CN207416,,C6920,,,277.89,,,
mondo:0020520,adult pulmonary Langerhans cell histiocytosis,"['PLCH', 'pulmonary Langerhans cell histiocytosis', 'pulmonary histiocytosis X', 'pulmonary eosinophilic granuloma']",,,99874,C3161104,,C142833,,,,J84.82,,
mondo:0020521,Ehlers-Danlos syndrome type 7A,['EDS VIIA'],,,99875,CN207418,"['0.4963', '0.3142', '-0.68', '0.4634', '0.3875', '-0.8125', '-0.01459', '0.3125', '-0.872', '0.603', '0.06866', '-0.225', '0.2686', '1.1455', '-0.4392', '-0.05554', '-0.749', '0.741', '0.1378', '-0.4739', '-0.0367', '0.844', '0.346', '0.033', '-0.2021', '0.07666', '0.2185', '0.10815', '1.613', '0.3652', '1.003', '-0.6694', '-0.004875', '-0.10724', '-0.0886', '0.1318', '-0.5073', '0.08685', '0.4543', '-1.059', '0.7993', '-0.4883', '-0.7324', '0.2164', '0.2441', '-0.8066', '-0.2202', '0.7637', '1.092', '-0.408', '-0.01515', '-0.2251', '0.552', '0.01034', '0.2097', '-0.3794', '-0.546', '0.8096', '0.5425', '-0.1249', '-0.08997', '0.4773', '0.2118', '-0.04218', '-0.1726', '0.4143', '-0.3242', '0.8647', '-0.5054', '1.124', '-0.6333', '0.11', '-0.541', '-0.649', '-0.1715', '0.002537', '-0.521', '0.2487', '0.10297', '-0.1815', '-0.5405', '-0.5977', '-0.05368', '0.4883', '-0.4521', '-0.339', '-0.064', '0.8706', '0.2197', '0.3105', '0.441', '0.3884', '-0.445', '0.623', '0.7437', '0.1942', '0.3914', '-0.4082', '-0.332', '-0.2126']",,,,,,,
mondo:0020522,Ehlers-Danlos syndrome type 7B,"['Ehlers-Danlos syndrome, type VIIB, autosomal dominant', 'EDS VIIB', 'EDSARTH2', 'Ehlers-Danlos syndrome, arthrochalasia type, 2']",,,99876,CN706304,"['0.5654', '0.292', '-0.672', '0.3965', '0.342', '-0.7236', '0.0761', '0.362', '-0.9253', '0.598', '0.0647', '-0.3022', '0.1498', '1.067', '-0.3474', '-0.1201', '-0.569', '0.587', '0.0146', '-0.603', '-0.05582', '0.858', '0.4048', '0.07825', '-0.2468', '0.0375', '0.1023', '0.102', '1.661', '0.328', '1.02', '-0.7573', '0.02818', '-0.0861', '-0.10364', '0.0979', '-0.557', '0.05716', '0.357', '-1.048', '0.7866', '-0.418', '-0.7065', '0.2834', '0.2578', '-0.7295', '-0.2168', '0.7324', '1.107', '-0.3044', '0.0551', '-0.2356', '0.611', '0.0988', '0.2632', '-0.3113', '-0.5054', '0.7676', '0.6016', '-0.09143', '-0.1181', '0.574', '0.1716', '-0.1005', '-0.05637', '0.4702', '-0.4016', '0.8203', '-0.3665', '1.272', '-0.4744', '0.07983', '-0.546', '-0.589', '-0.1871', '0.00804', '-0.48', '0.3086', '0.1353', '-0.154', '-0.566', '-0.5234', '0.1016', '0.4487', '-0.4153', '-0.3325', '-0.02292', '0.824', '0.2673', '0.2333', '0.348', '0.2922', '-0.5166', '0.614', '0.775', '0.1769', '0.3276', '-0.489', '-0.1952', '-0.1228']",,,C565061,,,,
mondo:0020523,familial parathyroid adenoma,['hereditary parathyroid gland adenoma'],,,99877,C1840403,,,,,,,,
mondo:0020524,primary parathyroid hyperplasia,"['familial parathyroids hyperplasia', 'hereditary parathyroids hyperplasia']",,,99878,,,,,,,,,
mondo:0020525,transient neonatal diabetes mellitus,"['chromosome 6-associated transient diabetes mellitus', 'diabetes mellitus, transient neonatal', 'transient neonatal diabetes mellitus', 'transient neonatal diabetes mellitus (disease)', 'TNDM', 'diabetes mellitus, 6q24-related transient neonatal']",0060334,,,,,C114899,,,,,,0008255
mondo:0020526,acute megakaryoblastic leukemia in down syndrome,['DS-AMKL'],,,99887,CN207426,,,,,,,,
mondo:0020527,ectopic Cushing syndrome,"['Cushing syndrome due to ectopic ACTH secretion', 'ectopic ACTH secreting tumour', 'occult ectopic ACTH secretion', 'ectopic Cushing syndrome', 'adrenocorticotropic hormone secretion syndrome', 'ectopic ACTH secreting tumor', 'paraneoplastic Cushing syndrome']",0060890,,99889,CN207427,,,,,,,,
mondo:0020528,ACTH-dependent Cushing syndrome,"['ACTH-dependent CS', 'overproduction of ACTH', 'adrenocorticotropic hormone-dependent Cushing syndrome', 'pituitary-dependent Cushing disease', 'pituitary Cushing disease', 'pituitary Cushing diseases', 'pituitary Cushing syndrome', 'ACTH hypersecretion, pituitary', 'corticotropin-dependent Cushing syndrome', 'adrenocorticotropic hormone, inappropriate secretion', 'pituitary-dependent Cushing^s disease']",3946,,99892,C0342442,,C113210,1001110,D047748,,E24.0,10035109,
mondo:0020529,ACTH-independent Cushing syndrome,"['adrenocorticotropic hormone-independent Cushing syndrome', 'corticotropin-independent Cushing syndrome', 'adrenal Cushing syndrome']",,,99893,CN207429,,,,,,,,
mondo:0020530,Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR1 deficiency,"['Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 1 deficiency', 'MSMD due to complete interferon gamma receptor 1 deficiency', 'MSMD due to complete IFNgammaR1 deficiency', 'interferon gamma, receptor 1, deficiency', 'IFNGR1 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency', 'IFNGR1 deficiency']",,,99898,C2930924,,,,C535530,,,,
mondo:0020531,long chain acyl-CoA dehydrogenase deficiency,"['inborn error of long-chain-acyl-CoA dehydrogenase activity', 'long-chain acyl-Coenzyme A dehydrogenase deficiency', 'ACADL deficiency', 'long-chain acyl-CoA dehydrogenase deficiency', 'LCAD', 'LCAD deficiency', 'acyl-CoA dehydrogenase, long-chain deficiency', 'rare inborn error of long-chain-acyl-CoA dehydrogenase activity']",,,99900,C0220711,,C84537,,C535690,,,,
mondo:0020532,spirillary rat-bite fever,"['Spirillary fever', 'spirillosis', 'sodoku', 'sodoku disease']",12096,,99903,,,,,,026.0,,,
mondo:0020533,streptobacillary rat-bite fever,"['Haverhill fever', 'Streptobacillosis', 'streptobacillary rat-bite fever', 'Streptobacillary fever']",13238,,99905,CN207435,,,,,026.1,,,
mondo:0020535,house allergic alveolitis,,,,99907,C4511048,,,,,,,,
mondo:0020537,occupational allergic alveolitis,,,,99909,,,,,,,,,
mondo:0020538,malignant dysgerminomatous germ cell tumor of ovary,"['malignant ovarian dysgerminoma', 'dysgerminomatous germ cell cancer of ovary', 'malignant dysgerminomatous germ cell tumour of the ovary', 'dysgerminomatous germ cell cancer of the ovary', 'malignant dysgerminomatous germ cell tumor of the ovary']",,,99912,CN207439,,,,,,,,
mondo:0020539,extragonadal non-dysgerminomatous germ cell tumor,,,,99913,CN207440,,,,,,,,
mondo:0020540,ovarian gynandroblastoma,"['Gynandroblastoma of ovary', 'Gynandroblastoma', 'Gynandroblastoma of the ovary']",,,99914,C0346178,,C3072,1000422,C538459,,,,
mondo:0020541,maligant granulosa cell tumor of ovary,"['malignant granulosa cell tumour of the ovary', 'malignant ovarian granulosa cell tumour', 'granulosa cell malignant tumour', 'malignant ovarian granulosa cell tumor', 'malignant granulosa cell tumor of ovary', 'Maligant granulosa cell tumour of the ovary', 'granulosa cell cancer', 'granulosa cell malignant tumor', 'granulosa theca cell tumor of the ovary', 'adult granulosa cell tumor of the ovary', 'granulosa theca cell tumour of the ovary', 'adult ovarian granulosa cell tumour', 'ovarian granulosa cell tumor of adults', 'malignant ovarian granulosa cell neoplasm', 'malignant granulosa cell neoplasm', 'adult ovarian granulosa cell tumor', 'malignant granulosa cell neoplasm of ovary', 'GCT of the ovary', 'cancer of granulosa cell', 'Maligant granulosa cell tumor of the ovary', 'granulosa theca cell tumour', 'ovarian granulosa cell tumour of adults', 'granulosa theca cell tumor', 'malignant granulosa cell tumor of the ovary', 'malignant granulosa cell tumour of ovary', 'malignant granulosa cell neoplasm of the ovary', 'adult granulosa cell tumour of the ovary', 'GTCT']",,,99915,CN207442,,C8403,,,,,,
mondo:0020542,malignant Sertoli-Leydig cell tumor of ovary,"['ovarian sertoli-Leydig cell tumor, malignant', 'virilizing ovarian tumour', 'ovarian Sertoli-Leydig cell tumor, malignant', 'ovarian Sertoli-Leydig cell cancer', 'malignant ovarian sertoli-Leydig cell tumour', 'Arrhenoblastoma', 'malignant ovarian Sertoli-Leydig cell tumour', 'virilizing ovarian tumor', 'malignant Sertoli-Leydig cell tumour of the ovary', 'ovarian malignant Sertoli-Leydig cell tumor', 'malignant Sertoli-Leydig cell tumor of the ovary', 'Androblastoma', 'ovarian malignant Sertoli-Leydig cell tumour']",,,99916,CN207443,,,,,239.5,,,
mondo:0020543,"theca steroid-producing cell malignant tumor of ovary, not further specified","['theca (steroid-producing) cell cancer, not further specified']",,,99917,CN207444,,,,,,,,
mondo:0020544,streptococcal toxic-shock syndrome,"['Streptococcus caused toxic shock syndrome', 'streptococcal TSS']",,,99918,C0343532,,,,,,,10044251,
mondo:0020545,staphylococcal toxic-shock syndrome,"['Staphylococcus caused toxic shock syndrome', 'staphylococcal TSS']",,,99919,,,,,,040.89,,10044250,
mondo:0020546,acute graft versus host disease,"['acute GVHD', 'GVHD, acute', 'graft versus host disease, acute', 'acute graft vs. host disease', 'fulminant graft versus host disease']",,,99920,C0856825,,C4980,0004599,,279.51,D89.810,10066260,
mondo:0020547,chronic graft versus host disease,"['GVHD, chronic', 'chronic GVHD', 'graft versus host disease, chronic']",,,99921,C0867389,,C4981,,,279.52,D89.811,10066261,
mondo:0020548,ocular pemphigoid,,,,99922,,,,,,,,10067776,
mondo:0020549,invasive hydatidiform mole,"['invasive Mole', 'invasive hydatidiform Mole', 'chorioadenoma', 'chorioadenoma Destruens', 'invasive gestational trophoblastic neoplasm', 'chorioadenoma destruens', 'invasive hydatidiform mole', 'IHM']",,,99925,C0008493,,C6985,,D002820,,,,
mondo:0020550,gestational choriocarcinoma,"['molar pregnancy with choriocarcinoma', 'gestational choriocarcinoma', 'gestational chorionepithelioma', 'gestational choriocarcinoma (morphologic abnormality)']",2025,,99926,C0349557,,C4646,,,181,,,
mondo:0020552,placental site trophoblastic tumor,"['placental-site GTT', 'placental site trophoblastic tumor (morphologic abnormality)', 'placental-site gestational trophoblastic tumor', 'placental-site gestational trophoblastic tumour', 'placental site trophoblastic tumor', 'placental site gestational trophoblastic tumour', 'placental site trophoblastic tumour (morphologic abnormality)', 'placental site gestational trophoblastic tumor', 'PSST', 'placental-site gestational trophoblastic neoplasm']",3596,,99928,C0206666,,C3757,1001111,D018245,,,,
mondo:0020553,secondary pulmonary hemosiderosis,,,,99930,C4274326,,,,,,,,
mondo:0020554,Heiner syndrome,['cow^s milk hypersensitivity'],,,99932,CN207456,,,,,518.89,,,
mondo:0020555,pleuropulmonary blastoma type 1,['type I pleuropulmonary blastoma'],,,99933,CN207457,,C45626,,,162.9,,,
mondo:0020556,pleuropulmonary blastoma type 2,['type II pleuropulmonary blastoma'],,,99934,CN207458,,C45627,,,162.9,,,
mondo:0020557,pleuropulmonary blastoma type 3,['type III pleuropulmonary blastoma'],,,99935,CN207459,,C45628,,,162.9,,,
mondo:0020558,autosomal dominant Charcot-Marie-Tooth disease type 2K,"['CMT2K', 'Charcot-Marie-Tooth disease type 2K']",,,99944,CN207468,,C133886,,,,,,
mondo:0020559,O^Sullivan-McLeod syndrome,,,,99965,C2721741,,,,,,,10069682,
mondo:0020560,atypical teratoid rhabdoid tumor,"['rhabdoid tumour of CNS', 'central nervous system rhabdoid neoplasm', 'primary malignant rhabdoid neoplasm of brain', 'atypical teratoid/rhabdoid tumour', 'primary malignant rhabdoid neoplasm of the brain', 'CNS rhabdoid neoplasm', 'malignant brain rhabdoid tumor', 'rhabdoid tumour of the central nervous system', 'atypical teratoid/rhabdoid tumour (WHO grade IV)', 'atypical teratoid/rhabdoid tumor (morphologic abnormality)', 'rhabdoid tumor predisposition syndrome', 'rhabdoid tumor of central nervous system', 'primary malignant rhabdoid tumour of brain', 'rhabdoid neoplasm of central nervous system', 'malignant rhabdoid neoplasm of brain', 'primary malignant brain rhabdoid neoplasm', 'atypical teratoid/rhabdoid tumor', 'central nervous system rhabdoid tumour', 'primary malignant rhabdoid tumor of brain', 'rhabdoid tumour of central nervous system', 'CNS rhabdoid tumor', 'rhabdoid tumour of the CNS', 'AT/RT', 'malignant brain rhabdoid tumour', 'ATT/RHT', 'primary malignant rhabdoid tumour of the brain', 'primary malignant brain rhabdoid tumor', 'rhabdoid neoplasm of the CNS', 'rhabdoid tumor of CNS', 'central nervous system rhabdoid tumor', 'malignant rhabdoid tumour of brain', 'atypical teratoid/rhabdoid tumour (morphologic abnormality)', 'malignant rhabdoid tumour of the brain', 'CNS rhabdoid tumour', 'malignant rhabdoid tumor of the brain', 'atypical teratoid/rhabdoid tumor (WHO grade IV)', 'ATRT', 'rhabdoid neoplasm of CNS', 'malignant rhabdoid neoplasm of the brain', 'rhabdoid tumor of the CNS', 'rhabdoid tumour predisposition syndrome', 'primary malignant brain rhabdoid tumour', 'primary malignant rhabdoid tumor of the brain', 'rhabdoid neoplasm of the central nervous system', 'rhabdoid tumor of the central nervous system', 'malignant rhabdoid tumor of brain', 'malignant brain rhabdoid neoplasm']",2129,,99966,CN207484,"['-0.1277', '0.2993', '0.0736', '-0.1414', '-0.0692', '-0.12384', '0.5366', '0.643', '-0.9204', '0.2632', '-0.06714', '-0.1768', '-0.1823', '0.2238', '0.275', '-0.1409', '-0.3726', '-1.14', '0.209', '-0.543', '0.1355', '-0.4116', '0.5503', '-0.705', '-0.1833', '-0.2162', '-0.347', '0.1267', '-0.3232', '0.03735', '0.6206', '-0.0999', '0.5957', '-0.4187', '-0.3699', '0.3657', '-0.273', '-0.2471', '-0.5786', '-0.04224', '0.2915', '-0.441', '0.3013', '-0.1169', '0.2427', '0.539', '0.03735', '0.03778', '-0.1387', '0.1687', '0.5107', '0.554', '-0.2842', '-0.1793', '-0.1284', '0.0652', '0.4883', '-0.07623', '-0.3027', '0.527', '0.09436', '0.0859', '-0.2888', '0.4128', '-0.3943', '0.0851', '0.2935', '-0.2112', '0.07623', '0.3835', '0.364', '0.559', '0.1719', '-0.4836', '0.1427', '0.3916', '0.4229', '-0.12036', '-0.667', '-0.6646', '-0.661', '-0.06464', '-0.02946', '0.7183', '-0.2493', '-0.3574', '0.258', '-0.1508', '0.3948', '-0.256', '0.1573', '0.1357', '0.3162', '-0.8154', '1.032', '-0.4602', '0.4138', '0.0643', '0.4146', '-0.06046']",C6906,1002008,,,,,
mondo:0020561,myxoid/round cell liposarcoma,"['MRCLS', 'myxoid/round-cell liposarcoma']",,,99967,,,,,,,,,
mondo:0020562,pleomorphic liposarcoma,"['PLS', 'pleomorphic liposarcoma (morphologic abnormality)', 'pleomorphic liposarcoma', 'PLLS']",5702,,99969,C0205825,,C3705,0003083,,171.9,,,
mondo:0020563,Dedifferentiated liposarcoma,"['DDLS', 'Dedifferentiated liposarcoma']",0080531,,99970,C0205824,,C3704,0003085,,171.9,,,
mondo:0020567,apnea of prematurity,,,,99981,,,C98823,,,,,,
mondo:0020568,cutaneous myiasis,,,,99983,C0027031,,,,,,B87.0,,
mondo:0020569,intermediate DEND syndrome,"['developmental delay-epilepsy-neonatal diabetes syndrome, intermediate form']",,,99989,CN207495,,,,,,,,
mondo:0020571,relapsing epidemic typhus,,,,99991,CN207497,,,,,,,,
mondo:0020572,complex regional pain syndrome type 2,"['CRPS II', 'Complex regional pain syndrome II', 'causalgia', 'Complex regional pain syndrome, type II']",3222,,99994,C0007462,,C121572,1000854,D002422,,,10064335,
mondo:0020573,inherited disease susceptibility,"['hereditary disease susceptibility', 'predisposition, genetic', 'susceptibilities, genetic', 'predispositions, genetic', 'genetic predispositions', 'genetic susceptibility', 'genetic susceptibilities', 'hereditary predisposition to disease', 'genetic predisposition', 'susceptibility, genetic']",,,,,,,,D020022,,Z15,,
mondo:0020574,central nervous system nongerminomatous germ cell tumor,"['nongerminomatous germ cell tumor of the CNS', 'nongerminomatous GCT - CNS', 'central nervous system nongerminomatous germ cell tumor', 'nongerminomatous germ cell tumour of the CNS']",,,,C1696109,,C100093,,,,,,
mondo:0020575,polymorphic ventricular tachycardia,['polymorphic ventricular tachycardia'],,,,C0344432,,C111648,,,,,,0031677
mondo:0020576,cutaneous vasculitis,['cutaneous vasculitis'],,,,C0262988,,C112210,,,,,,
mondo:0020577,childhood gonadal germ cell tumor,"['paediatric gonadal germ cell tumour', 'childhood gonadal germ cell tumor', 'gonadal germ cell tumor of childhood', 'pediatric gonadal germ cell tumor', 'gonadal germ cell tumour of childhood']",,,,C3899657,,C114801,,,,,,
mondo:0020579,mucositis,"['mucosa inflammation', 'mucositis']",,,,,,C115965,,D052016,,,,
mondo:0020580,germinomatous germ cell tumor,['germinomatous germ cell tumor'],,,,C4054897,,C121618,,,,,,
mondo:0020581,benign PEComa,"['neoplasm with perivascular epithelioid cell differentiation, benign', 'typical PEComa', 'benign PEComa', 'benign PEComa, nos', 'benign PEComa, not otherwise specified']",,,,C3839685,,C121791,,,,,,
mondo:0020582,benign uterine ligament neoplasm,['benign uterine ligament neoplasm'],,,,C0865093,,C126493,,,,,,
mondo:0020583,chromosome 17 disorder,['chromosome 17 abnormality'],,,,,,C129438,,,,,,
mondo:0020584,anemia due to enzyme disorder,['anemia due to enzyme disorder'],,,,C0494226,,C35472,,,,,,
mondo:0020585,anemia due to erythrocyte enzyme disorder,['anemia due to erythrocyte enzyme disorder'],,,,C4329304,,C131630,,,,,,
mondo:0020586,factor V deficiency,['factor V deficiency'],,,,,,C131738,,D005166,,,,
mondo:0020587,factor XI deficiency,['factor XI deficiency'],,,,,,C131739,,D005173,,,,
mondo:0020588,lung PEComa,"['lung PEComa', 'lung pecomatous tumour', 'lung pecomatous tumor']",,,,,,C142783,,,,,,
mondo:0020589,cardiac germ cell tumor,"['heart germ cell tumour', 'cardiac germ cell tumor', 'heart germ cell tumor']",,,,,,C147005,,,,,,
mondo:0020590,mycobacterial infectious disease,"['mycobacterial infection', 'mycobacterium infection']",,,,C0026918,,C26831,,D009164,,,,
mondo:0020592,disorder of pharynx,"['disorder of chordate pharynx', 'pharyngeal disorder', 'disease of chordate pharynx', 'chordate pharynx disease or disorder']",,,,,,C26850,,,,,,
mondo:0020593,trichoblastoma,"['Brooke^s tumor', 'trichoepithelioma', 'trichogenic adnexal tumour', 'trichogenic trichoblastoma', 'trichoepithelioma, benign', 'Brooke^s tumour', 'trichoblastoma', 'trichogenic adnexal tumor']",,,,,,C27132,,,,,,
mondo:0020594,abducens nerve disorder,"['VIth nerve disorder', 'abducens nerve disease', 'abducens nerve disease or disorder', 'abducens nerve disorder', 'disease of abducens nerve', 'disorder of abducens nerve']",,,,,,C27593,,,,,,
mondo:0020596,mucin-producing carcinoma,['mucin-producing carcinoma'],,,,,,C27825,,,,,,
mondo:0020597,angiokeratoma of scrotum,"['scrotal angiokeratoma', 'angiokeratoma of the scrotum', 'scrotal fordyce-type angiokeratoma', 'scrotum angiokeratoma', 'fordyce angiokeratoma', 'angiokeratoma of scrotum', 'fordyce-type angiokeratoma of scrotum', 'fordyce-type angiokeratoma of the scrotum', 'angiokeratoma of fordyce']",,,,,,C7752,,,,,,
mondo:0020598,malabsorption syndrome,"['malabsorption', 'malabsorption syndrome']",,,,C0024523,,C3214,,D008286,,,,
mondo:0020599,acquired coagulation factor deficiency,"['acquired coagulation protein disease', 'acquired coagulation factor deficiency']",,,,C0001169,,C34347,,,,,,
mondo:0020600,acute pharyngitis,"['acute pharyngitis', 'pharyngitis, acute']",,,,,,C34355,,,,,,
mondo:0020601,mosquito-borne viral encephalitis,['mosquito-borne viral encephalitis'],,,,,,C34823,,,,,,
mondo:0020602,Simpson-Golabi-Behmel syndrome type 1,"['Golabi-Rosen syndrome', 'Simpson-Golabi-Behmel syndrome type 1', 'dysplasia gigantism syndrome, X-linked', 'bulldog syndrome', 'DGSX Golabi-Rosen syndrome', 'Simpson-Golabi-Behmel syndrome, type 1, X-linked recessive', 'Sgbs', 'Simpson dysmorphia syndrome', 'Simpson-Golabi-Behmel syndrome, type 1', 'SGBS1', 'GPC3 Simpson-Golabi-Behmel syndrome']",0060248,312870,,,,,,,,,,
mondo:0020603,X-linked chondrodysplasia punctata 2,"['CDPXD', 'Conradi-Hunermann syndrome', 'Happle syndrome', 'X-linked chondrodysplasia punctata type 2', 'Conradi Hunermann syndrome', 'Conradi-Hünermann-Happle syndrome', 'Conrad Hunermann Happle syndrome', 'EBP chondrodysplasia punctata', 'chondrodysplasia punctata 2 X-linked dominant', 'Conradi-Hunermann-Happle syndrome', 'chondrodysplasia punctata, X-linked dominant, X-linked dominant', 'chondrodysplasia punctata 2, X-linked dominant', 'CDPX2']",0080352,302960,35173,,"['0.4937', '0.06445', '-0.1759', '-0.327', '0.2134', '0.0277', '0.2207', '0.809', '-0.2883', '-0.454', '-0.196', '0.4124', '0.248', '0.2262', '-0.0869', '0.082', '0.746', '-0.4111', '-0.4702', '-0.735', '-0.557', '-0.0745', '0.9126', '0.02109', '-0.287', '0.05756', '-0.554', '-0.1114', '-0.2058', '-0.4841', '0.3672', '-0.1576', '-0.01639', '0.1134', '0.2043', '0.4834', '-0.0653', '-0.434', '-0.1809', '0.182', '-0.1278', '-0.2323', '0.726', '0.2032', '0.005306', '-0.11786', '-0.2263', '0.367', '0.2773', '-0.02223', '-0.455', '-0.0411', '0.3547', '-0.599', '-0.5806', '-0.541', '0.6567', '-0.2307', '-0.07275', '-0.2683', '0.438', '0.02733', '-0.3452', '1.043', '0.1573', '0.4272', '0.2002', '0.4343', '0.1522', '0.3833', '0.2686', '0.2485', '0.2096', '-0.2192', '0.478', '0.0559', '-0.289', '-0.889', '-0.1931', '-0.4907', '-0.1827', '-0.698', '-0.05743', '0.9062', '-0.3965', '0.8237', '-0.05692', '0.2595', '-0.2327', '0.838', '0.0356', '0.4092', '0.1635', '0.662', '0.4165', '-0.529', '0.6294', '-0.2825', '0.2698', '-0.4648']",,,,,,,
mondo:0020604,X-linked dominant disease,,0080009,,,,,,,,,,,
mondo:0020605,X-linked recessive disease,,0080012,,,,,,,,,,,
mondo:0020606,sex-linked disease,,,,,,,,,,758.81,,,
mondo:0020607,Liddle syndrome 1,"['Liddle syndrome 1', 'SCNN1B Liddle syndrome', 'Liddle syndrome', 'LIDLS1', 'Pseudoaldosteronism']",,177200,,,,,,,,,,
mondo:0020627,"epileptic encephalopathy, infantile or early childhood",,,,,,,,,,,,,
mondo:0020628,"microcephaly, growth restriction, and increased sister chromatid exchange 2","['MGRISCE2', 'microcephaly, growth restriction, and increased sister chromatid exchange 2']",,618097,,,"['-0.0904', '0.098', '0.02925', '-0.06976', '0.05795', '-0.12177', '0.003248', '0.1748', '-0.1125', '-0.0671', '-0.05533', '0.0436', '0.05887', '-0.0017605', '-0.0446', '-0.0777', '0.0582', '-0.0325', '-0.03534', '-0.2103', '-0.0007725', '-0.0623', '0.1044', '-0.03632', '0.03796', '-0.0349', '-0.01055', '-0.01239', '-0.01828', '-0.08044', '0.1153', '-0.003206', '0.1416', '0.06885', '-0.006416', '-0.003963', '-0.006775', '-0.04547', '-0.00804', '-0.11487', '0.066', '-0.07227', '0.04813', '-0.03345', '-0.05267', '-0.1207', '-0.00969', '0.0811', '0.01868', '0.05008', '-0.05597', '-0.086', '-0.01663', '0.002153', '-0.0712', '-0.04724', '0.096', '-0.05734', '-0.1427', '0.02806', '0.07886', '0.0585', '-0.02809', '-0.0089', '0.03226', '0.000372', '0.1114', '0.0537', '-0.183', '0.1105', '-0.07306', '0.05615', '0.08124', '-0.0711', '0.06165', '0.02582', '-0.02074', '-0.04892', '-0.10767', '-0.05972', '-0.002172', '0.05542', '-0.07355', '0.05234', '-0.0677', '0.0401', '0.0428', '0.10443', '0.1768', '0.00896', '0.0358', '0.0661', '-0.04755', '-0.003567', '0.1964', '0.0517', '0.0737', '-0.1946', '-0.02176', '0.01527']",,,,,,,
mondo:0020629,"microcephaly, growth restriction and increased sister chromatid exchange",['MGRISCE'],,,,,,,,,,,,
mondo:0020630,"epileptic encephalopathy, infantile or early childhood, 1","['epileptic encephalopathy, infantile or early childhood, 1', 'IECEE1', 'developmental and epileptic encephalopathy 91']",0080472,617711,,,,,,,,,,
mondo:0020631,"epileptic encephalopathy, infantile or early childhood, 2","['IECEE2', 'developmental and epileptic encephalopathy 92', 'epileptic encephalopathy, infantile or early childhood, 2']",0080471,617829,,CN757794,,,,,,,,
mondo:0020632,"epileptic encephalopathy, infantile or early childhood, 3","['IECEE3', 'developmental and epileptic encephalopathy 93', 'epileptic encephalopathy, infantile or early childhood, 3']",0112275,618012,,CN248521,,,,,,,,
mondo:0020633,anaplastic cancer,['anaplastic malignant neoplasm'],,,,C1332287,,C36025,,,,,,
mondo:0020634,grade III meningioma,"['WHO grade III meningioma', 'grade 3 meningioma', 'grade III meningioma', 'meningioma, malignant']",,,,,,C38938,,,,,,
mondo:0020635,anaplastic meningioma,"['meningioma, anaplastic, malignant', 'malignant meningioma', 'meningioma, malignant', 'anaplastic (malignant) meningioma', 'anaplastic meningioma']",,,,,,C4051,,,,,,
mondo:0020636,Mendelian susceptibility to mycobacterial diseases due to a complete deficiency,,,,,,,,,,,,,
mondo:0020637,Mendelian susceptibility to mycobacterial diseases due to a partial deficiency,,,,,,,,,,,,,
mondo:0020638,superficial spreading melanoma,"['cutaneous superficial spreading melanoma', 'SSM', 'superficial spreading melanoma', 'superficial spreading cutaneous (skin) melanoma', 'superficial spreading melanoma of the skin', 'superficial spreading melanoma of skin', 'superficial spreading malignant skin melanoma', 'superficial spreading malignant melanoma of the skin', 'pagetoid melanoma', 'superficial spreading malignant melanoma of skin']",,,,,,C9152,,,,,,
mondo:0020639,monosomy,,,,,,,C3239,,D009006,,,,
mondo:0020640,autoimmune encephalitis,['autoimmune encephalitis'],,,622014,,,C122414,,,,,,
mondo:0020641,respiratory tract neoplasm,"['neoplasms, respiratory tract', 'tract neoplasms, respiratory', 'tumor of respiratory tract', 'tract neoplasm, respiratory', 'neoplasm of the respiratory tract', 'tumour of the respiratory tract', 'respiratory tract neoplasm', 'tumor of the respiratory tract', 'neoplasm, respiratory tract', 'neoplasm of respiratory tract', 'respiratory system neoplasm', 'tumour of respiratory tract', 'respiratory tract tumor', 'respiratory tract tumour']",,,,,,C3355,0003853,D012142,,C30-C39,,
mondo:0020642,polycystic kidney disease,"['fibrocystic renal disease', 'PKD - polycystic kidney disease', 'polycystic kidney disease']",0080322,,,,,C75464,,D007690,,,,
mondo:0020644,lung non-Hodgkin lymphoma,"['lung non-Hodgkin^s lymphoma', 'lung non-Hodgkin lymphoma', 'primary lung non-Hodgkin^s lymphoma']",,,,C1334453,,C5684,,,,,,
mondo:0020645,autosomal dominant osteopetrosis,"['OPTA', 'osteopetrosis (disease), autosomal dominant']",,,,C4272579,"['-0.0171', '0.0225', '0.01053', '-0.01328', '0.001638', '-0.03494', '0.010025', '0.03336', '-0.02757', '-0.02055', '-0.005642', '0.000995', '0.001407', '0.002993', '0.00392', '0.0029', '0.00839', '-0.0117', '-0.01149', '-0.0463', '-0.00498', '-0.005047', '0.01288', '-0.010506', '0.01714', '0.01015', '-0.005558', '-0.005424', '0.0003896', '-0.0118', '0.01607', '0.00976', '0.0177', '0.003466', '0.003332', '-0.0124', '0.003656', '-0.01799', '-0.001458', '-0.02235', '-0.00349', '-0.03', '0.01418', '-0.005795', '0.00442', '-0.02563', '0.0007744', '0.008446', '0.01431', '0.0004385', '0.006435', '-0.00835', '-0.002827', '-0.001944', '-0.003046', '-0.01907', '0.02856', '-0.002375', '-0.02377', '0.007034', '0.0184', '-0.002052', '0.004105', '-0.002102', '-0.000341', '-0.007454', '0.02007', '0.01357', '-0.01411', '0.02324', '-0.0299', '-0.002068', '0.012436', '-0.007378', '0.02544', '0.01643', '-0.002768', '0.006435', '-0.0191', '-0.02083', '-0.003275', '-0.001333', '0.007748', '0.01559', '0.003706', '0.000667', '0.01906', '0.02127', '0.010826', '0.01595', '0.01053', '0.00911', '-0.007996', '0.01408', '0.0441', '0.01116', '0.02074', '-0.0341', '-0.00592', '0.01602']",C129732,,,,,,
mondo:0020646,ocular adnexal lymphoma,"['OAL', 'ocular adnexa non-Hodgkin lymphoma', 'ocular adnexal lymphoma']",,,,C2981712,,C88145,,,,,,
mondo:0020647,"microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome","['microcephaly, facial dysmorphism, renal agenesis, and ambiguous genitalia syndrome', 'MFRG']",,618142,,,"['-0.07684', '0.1095', '0.03488', '-0.07697', '0.05505', '-0.0883', '-0.00834', '0.16', '-0.07837', '-0.0821', '-0.02565', '-0.0636', '-0.001599', '0.03052', '-0.0753', '-0.043', '0.02129', '-0.038', '-0.0583', '-0.1562', '0.025', '-0.001202', '0.0851', '-0.0166', '0.0779', '-0.04114', '-0.01775', '0.00986', '0.06683', '-0.0689', '0.0761', '-0.03848', '0.1571', '0.02452', '0.02744', '-0.02902', '-0.01837', '-0.04443', '-0.05145', '-0.0615', '0.05664', '-0.07465', '0.02481', '-0.04684', '-0.05756', '-0.1095', '-0.0464', '0.0783', '-0.03644', '0.04617', '-0.08057', '-0.03262', '0.00639', '-0.004337', '-0.0643', '-0.01093', '0.0515', '-0.0847', '-0.1256', '0.053', '0.061', '0.04703', '-0.02821', '0.0634', '-0.011795', '-0.00901', '0.09735', '0.1064', '-0.1265', '0.135', '-0.1089', '0.06165', '0.0662', '-0.0372', '0.00931', '-0.02504', '0.05743', '-0.0664', '-0.1029', '-0.0619', '-0.005604', '0.0571', '-0.02097', '0.05704', '-0.0268', '0.0194', '0.01327', '0.0845', '0.12286', '0.011986', '0.00685', '0.1304', '0.01562', '0.02072', '0.1885', '-0.002132', '0.09045', '-0.1348', '0.04742', '0.0812']",,,,,,,
mondo:0020648,rubella encephalitis,,,,,,,,,,,,,
mondo:0020649,warty carcinoma of the penis,"['condylomatous penile squamous cell carcinoma', 'warty carcinoma of the penis', 'warty penile squamous cell carcinoma', 'condylomatous carcinoma of penis', 'warty squamous cell carcinoma of the penis', 'squamous cell carcinoma of penis, condylomatous type', 'condylomatous squamous cell carcinoma of penis', 'condylomatous squamous cell carcinoma of the penis', 'squamous cell carcinoma of penis, warty type', 'squamous cell carcinoma of the penis, condylomatous type', 'squamous cell carcinoma of the penis, warty type', 'warty squamous cell carcinoma of penis', 'warty carcinoma of penis', 'condylomatous carcinoma of the penis']",,,,,,C6981,,,,,,
mondo:0020650,germ cell tumor of the vulva,,,,,,,,,,,,,
mondo:0020651,mixed germ cell tumor of vulva,,,,,,,,,,,,,
mondo:0020652,immature teratoma of vulva,,,,,,,,,,,,,
mondo:0020653,vaginal adenocarcinoma,"['adenocarcinoma of the vagina', 'adenocarcinoma of vagina', 'vaginal adenocarcinoma', 'vagina adenocarcinoma']",,,,,,C7981,,,,,,
mondo:0020654,renal pelvis/ureter urothelial carcinoma,"['renal pelvis and ureter transitional cell carcinoma', 'transitional cell cancer of the renal pelvis and ureter', 'renal pelvis and ureter urothelial carcinoma', 'TCC of the renal pelvis and ureter', 'renal pelvis and ureter transitional cell cancer', 'urothelial carcinoma of the renal pelvis and ureter', 'TCC of renal pelvis and ureter', 'transitional cell carcinoma of renal pelvis and ureter', 'renal pelvis and ureter TCC', 'transitional cell cancer of renal pelvis and ureter']",,,,,,C7716,,,,,,
mondo:0020655,juvenile ankylosing spondylitis,,0040092,,,,,,,,,,,
mondo:0020656,human papillomavirus-related penile squamous cell carcinoma,"['human papilloma virus-related penile squamous cell carcinoma', 'human papilloma virus related penile squamous cell carcinoma', 'HPV-related penile squamous cell carcinoma', 'human papillomavirus-related penile squamous cell carcinoma']",,,,,,C27682,,,,,,
mondo:0020657,human papillomavirus-related squamous cell carcinoma,"['human papillomavirus-related squamous cell carcinoma', 'human papilloma virus related squamous cell carcinoma', 'human papilloma virus-related squamous cell carcinoma', 'HPV-related squamous cell carcinoma']",,,,,,C27683,,,,,,
mondo:0020658,infiltrating ureter transitional cell carcinoma,,6845,,,,,,,,,,,
mondo:0020659,upper tract urothelial carcinoma,"['UTUC', 'transitional cell carcinoma of the upper urinary tract', 'transitional cell carcinoma of the pelvis and ureter']",,,598216,,,,,,,,,
mondo:0020660,osteoblastic osteosarcoma,['osteoblastic osteosarcoma'],,,,,,C53953,,,,,,
mondo:0020661,undifferentiated round cell sarcoma,['undifferentiated round cell sarcoma'],,,,,,C121799,,,,,,
mondo:0020662,borderline ovarian serous tumor,"['serous neoplasm of ovary with low malignant potential', 'serous tumour of the ovary with low malignant potential', 'ovarian serous tumor of low malignant potential', 'borderline serous neoplasm of the ovary', 'borderline ovarian serous tumor', 'borderline serous tumour of ovary', 'borderline serous tumor of the ovary', 'serous ovarian tumor of low malignant potential', 'serous ovarian tumour of low malignant potential', 'proliferating serous tumor of ovary', 'serous tumour of ovary with low malignant potential', 'serous neoplasm of the ovary with low malignant potential', 'borderline serous tumour of the ovary', 'borderline serous tumor of ovary', 'proliferating ovarian serous neoplasm', 'proliferating serous tumour of the ovary', 'borderline serous neoplasm of ovary', 'ovarian serous neoplasm of low malignant potential', 'serous ovarian neoplasm of low malignant potential', 'proliferating serous tumor of the ovary', 'proliferating serous tumour of ovary', 'serous tumor of the ovary with low malignant potential', 'proliferating ovarian serous tumour', 'proliferating serous neoplasm of ovary', 'serous tumor of ovary with low malignant potential', 'ovarian serous tumour of low malignant potential', 'borderline ovarian serous neoplasm', 'proliferating serous neoplasm of the ovary', 'proliferating ovarian serous tumor']",,,,,,C5226,,,,,,
mondo:0020663,malignant spindle cell neoplasm,"['spindle cell cancer', 'malignant spindle cell tumour', 'malignant spindle cell tumor', 'malignant spindle cell neoplasm']",,,,,,C27091,,,,,,
mondo:0020664,spindle cell neoplasm,"['spindle cell tumour', 'spindle cell tumor', 'spindle cell neoplasm']",,,,,,C27263,0000705,,,,,
mondo:0020665,high grade malignant neoplasm,['high grade malignant neoplasm'],,,,,,C36046,,,,,,
mondo:0020666,Löfgren syndrome,,,,,,,,,,,,,
mondo:0020667,Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis,"['ABS2', 'trapezoidocephaly-synostosis Syndrome', 'osteodysgenesis, multisynostotic, with fractures', 'Antley-Bixler syndrome without genital anomalies or disordered steroidogenesis', 'multisynostotic osteodysgenesis with long bone fractures']",0081290,207410,596008,,,,,,,,,
mondo:0020669,paranasal sinus cancer,"['malignant neoplasm of paranasal sinus', 'malignant tumor of the accessory sinus', 'malignant paranasal sinus tumor', 'malignant paranasal sinus neoplasm', 'malignant accessory sinus tumor', 'malignant accessory sinus tumour', 'malignant tumour of paranasal sinus', 'malignant tumour of the accessory sinus', 'malignant accessory sinus neoplasm', 'malignant tumour of the paranasal sinus', 'malignant tumour of accessory sinus', 'malignant paranasal sinus tumour', 'malignant neoplasm of accessory sinus', 'malignant neoplasm of the accessory sinus', 'malignant neoplasm of the paranasal sinus', 'malignant tumor of the paranasal sinus', 'malignant tumor of accessory sinus', 'malignant tumor of paranasal sinus']",,,,,,C7487,,,,,,
mondo:0020672,vascular occlusion disorder,['vascular occlusion'],,,,,,,,,,,,
mondo:0020673,arterial occlusion,"['arterial occlusion', 'arterial obstruction']",,,,,,C35318,,,,,,
mondo:0020674,vascular insufficiency disorder,,,,,,,,,,,,,
mondo:0020675,ischemic bowel disorder,"['ischemic bowel disease', 'ischaemic bowel disease']",,,,,,C35212,,,,,,
mondo:0020677,sudden hearing loss disorder,,,,,,,,,,,,,
mondo:0020678,sensorineural hearing loss disorder,"['sensorineural hearing loss', 'SNHL', 'sensorineural deafness']",10003,,,,,C26739,,,,,,0000407
mondo:0020679,conductive hearing loss disorder,"['conductive deafness', 'conductive hearing loss']",,,,,,C27645,,,,,,
mondo:0020680,acute bronchiolitis,"['Capillary pneumonia', 'acute capillary bronchiolitis', 'acute Bronchiolitis', 'acute bronchiolitis']",,,,C0001311,,C39659,,,466.19,,,
mondo:0020681,"Ehlers-Danlos syndrome, musculocontractural type 1","['Dundar syndrome', 'Ehlers-Danlos syndrome, type Vib, formerly', 'EDSMC', 'Arthrogryposis, Distal, with peculiar facies and hydronephrosis', 'adducted thumb, clubfoot, and Progressive Joint and skin laxity syndrome', 'EDSMC1', 'Ehlers-Danlos syndrome, type Vib', 'Ehlers-Danlos syndrome, musculocontractural type, 1', 'adducted thumb-clubfoot syndrome']",0080736,601776,,,,C168975,,,,,,
mondo:0020682,"Ehlers-Danlos syndrome, spondylodysplastic type, 1","['Ehlers-Danlos syndrome, progeroid type, 1, formerly', 'PDS, defective biosynthesis of', 'Ehlers-Danlos syndrome, spondylodysplastic type, 1', 'Ehlers-Danlos syndrome with Short stature and Limb anomalies', 'Ehlers-Danlos syndrome, progeroid type, 1', 'dermatan sulphate proteoglycan', 'galactosyltransferase 1 deficiency', 'xylosylprotein 4-Beta-galactosyltransferase deficiency', 'proteodermatan sulfate, defective biosynthesis of', 'EDSSPD1', 'dermatan sulfate proteoglycan', 'XGPT deficiency']",0080738,130070,,,,,,,,,,
mondo:0020683,acute disease,"['acute diseases', 'acute disease', 'disease, acute']",,,,C0001314,,,,D000208,799.89,,,
mondo:0020684,"Ehlers-Danlos syndrome, periodontal type 1","['EDSPD1', 'Ehlers-Danlos syndrome, type 8', 'Ehlers-Danlos syndrome, periodontosis type', 'EDS 8', 'Ehlers-Danlos syndrome, periodontitis type', 'Ehlers-Danlos syndrome, periodontal type, 1']",0080986,130080,,,,,,,,,,
mondo:0020685,infratentorial ependymal tumor,['infratentorial ependymal tumor'],,,,,,C131612,,,,,,
mondo:0020686,acute tonsillitis,"['infective tonsillitis', 'acute tonsillitis']",,,,C0001361,,C97142,,,463,,,
mondo:0020687,supratentorial ependymal tumor,['supratentorial ependymal tumor'],,,,,,C131611,,,,,,
mondo:0020688,spinal cord ischemia,"['ischemic myelopathy', 'ischemias, spinal cord', 'spinal cord Ischemias', 'cord ischemia, spinal', 'cord Ischemias, spinal', 'ischemic myelopathies', 'spinal cord ischemia, experimental', 'myelopathies, ischaemic', 'myelopathy, ischaemic', 'ischaemic myelopathy', 'experimental spinal cord ischemia', 'ischaemic myelopathies', 'myelopathy, ischemic', 'myelopathies, ischemic', 'ischemia, spinal cord']",,,,,,,,D020760,,,,
mondo:0020689,AIDS dementia complex,"['HIV-1-Associated Cognitive Motor Complex', 'Encephalopathies, AIDS', 'HIV Encephalopathy', 'Acquired immune deficiency syndrome dementia complex', 'AIDS related Dementia Complex', 'HIV-associated dementia', 'HIV ASSOC COGNITIVE MOTOR COMPLEX', 'Dementia Complex, AIDS', 'Complex, AIDS-related Dementia', 'HIV associated cognitive and motor complex', 'AIDS with dementia (disorder)', 'AIDS dementia complex', 'HIV Dementias', 'HIV encephalitis', 'HIV Dementia', 'Dementias, HIV', 'AIDS dementia', 'HIV 1 Cognitive and Motor Complex', 'DEMENTIA COMPLEX ACQUIRED IMMUNE DEFIC SYNDROME', 'Acquired-Immune Deficiency Syndrome Dementia Complex', 'Encephalopathy, AIDS', 'AIDS - Acquired immune deficiency syndrome dementia complex', 'HIV 1 Associated Cognitive Motor Complex', 'Acquired immune deficiency syndrome-related dementia', 'Dementia Complex, AIDS related', 'Complex, AIDS Dementia', 'AIDS Dementia Complex', 'AIDS Encephalopathy', 'HIV-Associated Cognitive Motor Complex', 'Dementia associated with acquired immunodeficiency syndrome', 'AIDS-related Dementia Complex', 'Dementia, HIV', 'AIDS related cognitive impairment', 'HIV Encephalopathies', 'AIDS Encephalopathies', 'ADC - Acquired immune deficiency syndrome dementia complex', 'Dementia associated with AIDS', 'Encephalopathy, HIV', 'Encephalopathies, HIV', 'ADC', 'Dementia Complex, AIDS-related', 'AIDS Dementia', 'Dementia Complex, Acquired Immune Deficiency Syndrome', 'AIDS RELAT DEMENTIA COMPLEX', 'HIV Associated Cognitive Motor Complex', 'DEMENTIA COMPLEX AIDS RELAT', 'HIV-1 Cognitive and Motor Complex']",,,,C0001849,,C2864,0002608,D015526,294.8,,,
mondo:0020690,adult glioblastoma,"['grade IV adult astrocytic tumor', 'glioblastoma', 'adult glioblastoma multiforme', 'grade IV adult astrocytic tumour', 'adult glioblastoma', 'grade IV adult astrocytic neoplasm']",,,,,,C9094,,,,,,
mondo:0020692,"spondylocostal dysostosis 1, autosomal recessive","['spondylocostal dysostosis 1, autosomal recessive', 'vertebral anomalies', 'spondylothoracic dysostosis', 'spondylothoracic dysplasia', 'SCDO1']",0112365,277300,,,,,,,,,,
mondo:0020693,glycogen storage disease due to liver phosphorylase kinase deficiency,,,,264580,,"['-0.3083', '0.0764', '-0.07117', '-0.6113', '0.644', '-0.3416', '-0.255', '0.9536', '-0.1423', '0.3704', '-0.4', '-0.02946', '-0.0358', '-0.1016', '-0.1884', '0.123', '-0.1948', '-0.3645', '-0.749', '-0.15', '0.2008', '-0.5', '0.538', '0.04117', '-0.372', '-0.592', '-0.1197', '-0.622', '-0.0958', '-0.4', '0.51', '0.2085', '0.321', '0.1252', '-0.479', '-0.1559', '-0.382', '-0.0519', '0.09937', '-0.07117', '-0.2345', '-0.03525', '-0.1562', '0.3672', '-0.6562', '0.1359', '0.1271', '0.01567', '-0.279', '0.5103', '0.2974', '-0.1156', '0.3035', '-0.0946', '-0.2294', '-0.4883', '-0.02066', '-0.293', '-0.4878', '0.388', '0.129', '-0.1606', '0.2852', '-0.417', '-0.10565', '0.712', '0.3809', '0.2118', '-0.5513', '0.2964', '-0.08167', '-0.0827', '0.1287', '0.2563', '0.2988', '0.2255', '0.1626', '-0.0721', '-0.7217', '0.4512', '-0.1809', '-0.007626', '-0.10333', '-0.368', '-0.01231', '0.59', '0.3809', '-0.2957', '0.8833', '0.362', '0.375', '0.742', '-0.3738', '-0.2915', '0.4731', '0.68', '0.566', '-0.529', '-0.00716', '-0.1554']",,,,,,,
mondo:0020694,salivary gland epithelial myoepithelial carcinoma,['salivary gland epithelial myoepithelial carcinoma'],,,,,,C35701,,,,,,
mondo:0020695,hypotonic cerebral palsy,['hypotonic cerebral palsy'],,,,,,C116906,,,,,,
mondo:0020696,vitamin B12 deficiency,"['vitamin b12 deficiency', 'hypocobalaminemia']",,,,C0042847,,C131684,,D014806,266.2,,,0100502
mondo:0020697,lung epithelial-myoepithelial carcinoma,"['lung epithelial-myoepithelial carcinoma', 'lung epithelial-myoepithelial cancer']",,,,,,C45545,,,,,,
mondo:0020698,inborn error of biotin metabolism,,,,,,,,,,,,,
mondo:0020699,biotin metabolic disease,,,,,,,,,,,,,
mondo:0020701,brachydactyly type A1A,"['Farabee-type Brachydactyly', 'BDA1', 'BRACHYDACTYLY, type A1']",,,,,,,,,,,,
mondo:0020702,autosomal dominant epidermolytic ichthyosis,,,,,,,,,,,,,
mondo:0020703,erythroid neoplasm,"['erythroid tumour', 'erythroid neoplasm', 'erythroid tumor']",,,,,,C7064,,,,,,
mondo:0020704,inherited rippling muscle disease,"['RMD', 'rippling muscle disease']",,,,,,,,,,,10069417,
mondo:0020705,"neural tube defects, susceptibility to","['neural tube defects', 'NTD', 'spina bifida, susceptibility to', 'spina bifida', 'neural tube defects, SUSCEPTIBILITY to']",,182940,,,"['-0.0656', '0.05936', '0.0601', '-0.05264', '0.1306', '-0.1431', '0.0226', '0.07715', '-0.05557', '-0.07056', '-0.03824', '-0.01474', '-0.001566', '0.0595', '-0.102', '-0.07043', '-0.01503', '-0.0672', '-0.1016', '-0.1242', '0.05252', '-0.03397', '0.09564', '-0.0359', '-0.05667', '-0.04807', '0.01915', '0.01234', '0.01938', '-0.06964', '0.11816', '-0.02516', '0.1053', '0.03778', '0.04993', '-0.005177', '-0.01884', '-0.01313', '-0.04214', '-0.1123', '0.0698', '-0.05316', '0.0683', '-0.01337', '-0.07007', '-0.1475', '0.03293', '0.0208', '0.00326', '0.08325', '-0.06012', '-0.0715', '0.05496', '0.00754', '-0.06573', '-0.02083', '0.0667', '0.003271', '-0.08325', '0.02779', '0.04865', '0.02069', '-0.00952', '0.06744', '0.015495', '0.09937', '0.1058', '0.0929', '-0.134', '0.1251', '-0.06046', '-0.014275', '-0.02667', '-0.0779', '0.00259', '0.03049', '0.0325', '-0.05295', '-0.02274', '-0.02527', '-0.04337', '0.03476', '-0.01512', '0.10803', '-0.0707', '0.001126', '0.05563', '0.0763', '0.1387', '-0.02072', '0.03378', '0.11523', '-0.011765', '0.00555', '0.1991', '0.01819', '0.0776', '-0.1178', '-0.03345', '0.02222']",,,,,,,
mondo:0020706,Heberden^s node,"['Heberden^s node', 'tuberculum arthriticum']",,,,,,C34671,,,,,,
mondo:0020707,central hearing loss,['central hearing loss'],,,,,,C34662,,,,,,
mondo:0020708,brachial amyotrophic diplegia,"['BAD', 'man-in-barrel syndrome', 'brachial amyotrophic diplegia', 'FAS', 'flail arm syndrome']",,,,,,C133085,,,,,,
mondo:0020709,Majocchi granuloma,['Majocchi^s granuloma'],,,,,,,,,,,,
mondo:0020710,amnionitis,"['amnionitis', 'Infection of amniotic cavity', 'amnionitides', 'amniotic cavity infection', 'amniotic infection syndrome']",,,,C0002631,,C50459,,,658.40,,,
mondo:0020711,selective peripheral resistance to thyroid hormone,['PerRTH'],,,,,,,,,,,,
mondo:0020712,"46,XY sex reversal 1","['46,XY true hermaphroditism, SRY-related', '46,XY gonadal dysgenesis, complete, SRY-related', '46XY sex reversal 1, Y-linked', '46,XY sex reversal 1', '46,XY sex reversal type 1', '46,XY sex reversal, SRY-related', 'SRXY1']",0111778,400044,,,,C128188,,,,,,
mondo:0020713,pulmonary venoocclusive disease 1,"['PVOD1', 'pulmonary venoocclusive disease 1, autosomal dominant']",0081268,265450,,,,,,,,,,
mondo:0020714,"mitochondrial myopathy, episodic, with optic atrophy and reversible leukoencephalopathy",,,251900,,,,,,,,,,
mondo:0020715,"multiple system atrophy 1, susceptibility to","['multiple system atrophy, susceptibility to', 'MSA1, susceptibility to', 'MSA1', 'multiple system atrophy 1, susceptibility to']",,146500,,,,,,,,,,
mondo:0020716,familial thyroid dyshormonogenesis 1,"['hypothyroidism, congenital, due to dyshormonogenesis, 1', 'thyroid hormonogenesis, genetic defect in, 1', 'TDH1', 'thyroid dyshormonogenesis 1', 'thyroid dyshormonogenesis type 1', 'iodine accumulation, transport, or trapping defect']",0112185,274400,,,,,,,,,,
mondo:0020717,autosomal dominant wooly hair,"['wooly hair, autosomal dominant', 'ADWH', 'woolly hair, autosomal dominant']",0111573,194300,,,,,,,,,,
mondo:0020718,"congenital short bowel syndrome, autosomal recessive","['congenital short bowel syndrome due to CLMP variation', 'CSBS', 'congenital short bowel syndrome']",,615237,,C0021847,,,,,,,,
mondo:0020720,X-linked hypophosphatemic rickets,['X-linked hypophosphatemic rickets (recessive or dominant)'],,,,C3540852,,C123265,,D053098,,,,
mondo:0020721,X-linked sideroblastic anemia 1,"['X chromosome-linked sideroblastic anemia', 'X-linked sideroblastic anaemia', 'X chromosome-linked sideroblastic anaemia', 'anemia, sideroblastic, 1, X-linked recessive', 'anemia sex-linked hypochromic sideroblastic', 'anaemia sex-linked hypochromic sideroblastic', 'sideroblastic anaemia X-linked', 'anaemia hereditary sideroblastic', 'anemia, hypochromic', 'X-linked sideroblastic anemia', 'ANH1', 'sideroblastic anemia X-linked', 'anemia, hereditary sideroblastic', 'anemia, sideroblastic, 1', 'hereditary iron-loading Anaemia', 'anemia hereditary sideroblastic', 'anemia, sideroblastic, X-linked', 'hereditary iron-loading Anemia', 'SIDBA1', 'erythroid 5-aminolevulinate synthase deficiency', 'XLSA', 'sideroblastic anemia, X-linked']",0060063,300751,75563,C0221018,"['-0.4734', '0.449', '-0.3855', '0.3455', '0.5615', '0.2301', '-0.2026', '0.6074', '-0.2585', '-0.3206', '0.5728', '-0.0702', '0.3394', '0.4395', '-1.185', '0.1081', '-0.6167', '0.0634', '-0.4072', '-0.489', '-0.10425', '-0.4705', '0.4043', '-0.2272', '0.561', '-0.3167', '0.00667', '-0.2216', '0.529', '0.10406', '0.355', '0.166', '0.442', '0.6294', '0.298', '-0.3003', '-0.921', '-0.591', '0.4985', '-0.09784', '-0.545', '0.3809', '0.0609', '-0.3818', '-0.643', '-0.8003', '0.0737', '-0.077', '0.2705', '-0.508', '0.3513', '0.4375', '0.905', '-0.1014', '0.643', '-0.615', '0.1172', '0.3003', '-1.212', '-0.1141', '-0.0396', '0.354', '-0.05716', '-0.2493', '-0.0658', '0.287', '0.1813', '0.833', '-0.5493', '0.9463', '0.8257', '-0.3315', '-0.495', '-0.5317', '0.3792', '0.7637', '0.2401', '0.00714', '-0.02019', '0.1456', '0.04175', '-0.0425', '-0.1304', '-0.1342', '0.3838', '-0.01616', '-0.4846', '0.2393', '0.697', '-0.3428', '0.799', '0.204', '-0.3079', '-0.2242', '0.6206', '0.963', '0.02895', '0.2388', '0.3018', '-0.3174']",,,C536761,,,,
mondo:0020722,nephrolithiasis susceptibility caused by SLC26A1,"['urolithiasis, calcium oxalate', 'nephrolithiasis, calcium oxalate', 'CAON']",0080652,167030,,C1833683,,,,,,,,
mondo:0020723,"vitamin D-dependent rickets, type 1A","['pseudovitamin D-deficiency rickets, type 1A', '25-hydroxycholecalciferol-1-Hydroxylase deficiency', '1-Alpha-Hydroxylase deficiency', 'VDDR1A', 'PDDR 1A', 'vitamin D-dependent rickets, type I', 'vitamin D-dependent rickets, type 1A', 'vitamin D hydroxylation-deficient rickets, type 1A', 'vitamin D dependency, type 1', '1-Alpha, 25-Hydroxyvitamin D3 deficiency, selective']",0080886,264700,,C0268689,,,,,,,,
mondo:0020724,cerebral cavernous malformation 1,"['cerebral cavernous malformations', 'cerebral cavernous malformations 1', 'cavernous angiomatous malformations', 'cerebral capillary malformations', 'cavernous malformations of CNS and retina', 'cavernous angioma, familial', 'familial cerebral cavernous malformation 1', 'hyperkeratotic cutaneous capillary-Venous malformations associated with cerebral capillary malformations', 'cerebral cavernous malformations-1', 'CCM']",0080491,116860,,,,,,,,,,
mondo:0020725,anemia due to chronic disorder,"['anaemia due to Chronic Disorder', 'anemia of chronic illness', 'anemia of systemic disease', 'anaemia of chronic illness', 'anemia due to chronic disorder', 'anaemia of chronic disease', 'Secondary anaemia', 'Secondary anemia', 'anemia due to Chronic Disorder', 'anaemia of chronic disorder', 'anemia of chronic disease', 'anaemia of systemic disease', 'anemia of chronic disorder', 'anaemia of chronic inflammation', 'anemia of chronic inflammation']",,,,C0002873,,C35659,,,285.29,,,
mondo:0020726,"tubulointerstitial kidney disease, autosomal dominant, 2","['ADMCKD1', 'medullary cystic kidney disease, autosomal dominant', 'medullary cystic kidney disease 1', 'medullary cystic kidney disease type 1', 'Mckd', 'MUCI-related ADTKD', 'polycystic kidneys, medullary type', 'ADTKD-MUC1', 'autosomal dominant medullary cystic kidney disease without hyperuricemia', 'MUC1-related autosomal dominant medullary cystic kidney disease', 'MUC1-related autosomal dominant tubulointerstitial kidney disease', 'autosomal dominant tubulointerstitial kidney disease due to mutations in MUC1', 'MCKD1']",,174000,88949,CN206321,,C123171,,,,,,
mondo:0020727,combined oxidative phosphorylation deficiency 22,"['combined oxidative phosphorylation deficiency type 22', 'COXPD22', 'combined oxidative phosphorylation deficiency 22']",0111498,616045,,,,,,,,,,
mondo:0020728,"hypouricemia, renal 1","['Dalmatian hypouricemia', 'hypouricemia, renal', 'hypouricemia, renal, type 1', 'RHUC1', 'hypouricemia, renal, 1', 'renal hypouricemia']",,220150,,C0473219,,,,,,,,
mondo:0020729,autosomal recessive agammaglobulinemia 1,"['agammaglobulinemia 1, autosomal recessive', 'agammaglobulinemia, autosomal recessive, due to IGHM defect', 'AGM1']",0081136,601495,,,,,,,,,,
mondo:0020730,carpal tunnel syndrome 1,"['CTS1', 'CTS', 'amyotrophy, thenar, of carpal origin', 'carpal tunnel syndrome', 'carpal tunnel syndrome, familial']",,115430,,,,,,,,,,
mondo:0020731,arbovirus infection,"['ARBOVIRUS INFECT', 'Arbovirus Infections', 'Infections, Arbovirus', 'Arbovirus infection', 'Arbovirus Infection', 'Infection, Arbovirus', 'arthropod-borne viral infection', 'Arboviral disease', 'Arthropod-borne viral infection', 'arbovirus infection', 'Arthropod-Borne Viral Infection']",,,,C0003723,,C34396,1001269,D001102,,,,
mondo:0020732,progeria,,,,,,,,,D011371,,,,
mondo:0020733,proximal symphalangism 1A,"['SYM1A', 'Sym1', 'symphalangism, proximal, type 1A', 'hereditary absence of the proximal interphalangeal joints', 'symphalangism, proximal, 1A', 'Cushing symphalangism']",0080787,185800,,C3714899,,,,,,,,
mondo:0020735,ACTH-independent macronodular adrenal hyperplasia 1,"['Cushing syndrome, adrenal, due to AIMAH', 'AIMAH1', 'corticotropin-independent macronodular adrenal hyperplasia', 'ACTH-independent macronodular adrenal hyperplasia, Somatic mutation', 'ACTH-independent macronodular adrenocortical hyperplasia', 'adrenocorticotropic hormone-independent macronodular adrenal hyperplasia', 'ACTH-independent macronodular adrenal hyperplasia']",0111623,219080,,C1857451,,,,,,,,
mondo:0020736,uncombable hair syndrome 1,"['UHS1', 'uncombable hair syndrome 1', 'uncombable hair syndrome', 'pili trianguli Et canaliculi']",,191480,,,,,,,,,,
mondo:0020737,"optic atrophy 10 with or without ataxia, intellectual disability, and seizures","['optic atrophy 10 with or without ataxia, intellectual disability, and seizures', 'optic atrophy 10 with or without ataxia, mental retardation, and seizures', 'OPA10']",0111434,616732,,,,,,,,,,
mondo:0020738,multiple benign circumferential skin creases on limbs 1,"['skin creases, congenital symmetric circumferential, 1', 'symmetric circumferential skin creases, congenital, 1', 'CSCSC1']",0112242,156610,,,,,,,,,,
mondo:0020739,"hypercalcemia, infantile, 1","['hypercalcemia, infantile, 1', 'HCINF1']",,143880,,C0268080,,,,,,,,
mondo:0020740,ectodermal dysplasia and immunodeficiency 1,"['ectodermal dysplasia and immunodeficiency 1, X-linked recessive', 'ectodermal dysplasia, hypohidrotic, with immune deficiency 1', 'EDAID1', 'HED-Id', 'ectodermal dysplasia, anhidrotic, with immune deficiency 1', 'EDA-Id']",0081078,300291,,,,C176592,,,,,,
mondo:0020741,pyridoxine-dependent epilepsy caused by ALDH7A1 mutant,"['Epd', 'pyridoxine-dependent epilepsy', 'EPD', 'AASA dehydrogenase deficiency', 'epilepsy, pyridoxine-dependent', 'pyridoxine dependency with seizures']",,266100,,,,,,,,,,
mondo:0020743,mixed phenotype acute leukemia,"['mixed phenotype acute leukemia', 'MPAL']",,,530995,,,C82179,,,,,10067399,
mondo:0020744,Mobitz type I atrioventricular block,"['AV block second degree Mobitz type I', 'type 1 2nd degree AV block', 'second degree atrioventricular block Möbitz type I', 'AV block second degree Möbitz type I', 'Möbitz I', 'type 1 second degree atrioventricular block', 'type 1 second degree AV block', 'Mobitz type I', 'Mobitz type I second degree AV block', 'Möbitz type I second degree AV block', 'Mobitz I', 'second degree atrioventricular block Mobitz type I', 'Wenckebach block']",,,,,,C62017,,,,,,
mondo:0020745,ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome,"['cardiac arrhythmia', 'autosomal dominant cardiac arrhythmia (Kuhn)', 'ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome', 'VACRDS', 'extrasystoles']",,115000,,C5542154,,,,,,,,
mondo:0020746,"contractures, pterygia, and variable skeletal fusions syndrome 1B","['contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B']",0081322,618469,,,,,,,,,,
mondo:0020747,sitosterolemia 1,['STSL1'],,210250,,,,,,,,,,
mondo:0020748,sitosterolemia 2,['STSL2'],,618666,,,,,,,,,,
mondo:0020749,polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 1,,,221770,,,,,,,,,,
mondo:0020750,polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy 2,,,618193,,,,,,,,,,
mondo:0020751,orthostatic hypotension 2,,,618182,,,,,,,,,,
mondo:0020752,"myoclonic epilepsy, juvenile, susceptibility to, 1",['EJM1'],,,,,,,,,,,,
mondo:0020753,Orthocoronavirinae infectious disease,['coronavirus infectious disease'],0080599,,,,,,,,,,,
mondo:0020754,visceral myopathy 1,"['pseudoobstruction, idiopathic intestinal', 'infantile visceral myopathy', 'visceral myopathy', 'visceral myopathy 1', 'VSCM', 'megaduodenum and/or megacystis']",,155310,,,,,,,,,,
mondo:0020756,"migraine, familial hemiplegic, 1","['MHP1', 'hemiplegic migraine, familial type 1', 'migraine, familial hemiplegic, 1, with progressive cerebellar ataxia', 'migraine, familial hemiplegic, type 1', 'migraine, familial hemiplegic 1, with progressive cerebellar ataxia', 'migraine, familial hemiplegic, 1', 'FHM1', 'migraine, sporadic hemiplegic', 'familial hemiplegic migraine type 1']",0111181,141500,,,,,,C536890,,,,
mondo:0020757,sporadic hemiplegic migraine,['sporadic hemiplegic migraine'],,,,,,C117011,,,,,,
mondo:0020759,"epilepsy, childhood absence, susceptibility to, 1","['epilepsy, childhood absence, susceptibility to, 1', 'ECA1', 'epilepsy, childhood absence, 1']",,600131,,,,,,,,,,
mondo:0020760,skin squamous cell carcinoma in situ,"['squamous cell carcinoma in situ of the skin', 'skin squamous cell carcinoma in situ', 'intraepidermal squamous cell carcinoma', 'squamous cell carcinoma in situ of skin', 'skin squamous cell cancer in situ']",,,,,,C2906,,,,,,
mondo:0020761,Bowen disease of the skin,"['Bowen disease', 'Disease, Bowen^s', 'intraepidermal squamous cell carcinoma, Bowen type', 'Disease, Bowen', 'Bowens Disease', 'Bowen disease of the skin', 'Bowen^s disease of the skin', 'Bowen Disease']",,,,C0006079,,C62571,,D001913,,,,
mondo:0020762,diencephalic-mesencephalic junction dysplasia syndrome 2,"['DMJDS2', 'spastic tetraparesis, dystonia, developmental delay, and structural abnormalities of the basal ganglia']",,618646,,,,,,,,,,
mondo:0020763,Menke-Hennekam syndrome 1,"['Menke-Hennekam syndrome 1', 'MKHK1']",,618332,,,,,,,,,,
mondo:0020764,Brown-Pearce carcinoma,"['Brown-Pearce epithelioma', 'Brown-Pearce tumour', 'Brown-Pearce carcinoma', 'carcinoma, Brown-Pearce', 'epithelioma, Brown Pearce', 'epithelioma, Brown-Pearce', 'carcinoma, Brown Pearce']",,,,C0007122,,,1001278,D002284,,,,
mondo:0020765,"neuropathy, congenital hypomyelinating, 2","['NEUROPATHY, CONGENITAL HYPOMYELINATING, 2', 'CHN2', 'hypomyelinating neuropathy, congenital, 2']",,618184,,,,,,,,,,
mondo:0020766,"neuropathy, congenital hypomyelinating, 3","['CHN3', 'hypomyelinating neuropathy, congenital, 3', 'NEUROPATHY, CONGENITAL HYPOMYELINATING, 3']",,618186,,,,,,,,,,
mondo:0020767,cauda equina syndrome with neurogenic bladder,"['Cauda Equina Syndrome with Neurogenic Bladder', 'cauda equina syndrome with neurogenic bladder', 'Cauda equina syndrome with neurogenic bladder']",,,,C0007459,,C34453,,,344.61,,,
mondo:0020768,X-linked deafness,"['deafness, X-linked, DFN', 'deafness, X-linked', 'DFNX']",,,,,,,,,,,,
mondo:0020769,Menke-Hennekam syndrome 2,"['MKHK2', 'Menke-Hennekam syndrome 2']",,618333,,,,,,,,,,
mondo:0020770,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 3","['SCAN3', 'SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE, WITH AXONAL NEUROPATHY 3']",,618387,,,,,,,,,,
mondo:0020771,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy",['SCAN'],,,,,,,,,,,,
mondo:0020772,"epilepsy, juvenile absence, susceptibility to, 1","['JAE1', 'EJA1', 'EPILEPSY, JUVENILE ABSENCE, SUSCEPTIBILITY TO, 1']",0111324,607631,,,,,,,,,,
mondo:0020773,cerebrospinal fluid rhinorrhea,"['Rhinorrhea, Spontaneous Cerebrospinal Fluid', 'Cerebrospinal Fluid Rhinorrhea, post Traumatic', 'Rhinorrhea, Traumatic Cerebrospinal Fluid', 'Rhinorrheas, CSF', 'Traumatic Rhinorrhea, Cerebrospinal Fluid', 'Rhinorrheas, Cerebrospinal', 'Rhinorrhea, Cerebrospinal', 'Traumatic Cerebrospinal Fluid Rhinorrhea', 'Cerebrospinal rhinorrhea', 'post-Traumatic Cerebrospinal Fluid Rhinorrhea', 'Cerebrospinal fluid rhinorrhoea', 'CSF Rhinorrheas', 'CSF rhinorrhoea', 'Rhinorrheas, Cerebrospinal Fluid', 'post Traumatic Cerebrospinal Fluid Rhinorrhea', 'Rhinorrhea, Cerebrospinal Fluid', 'CSF - Cerebrospinal rhinorrhea', 'Rhinorrhea, Cerebrospinal Fluid, Spontaneous', 'Rhinorrhea, post-Traumatic, Cerebrospinal Fluid', 'Cerebrospinal Fluid Rhinorrhea, Spontaneous', 'Spontaneous Rhinorrhea, Cerebrospinal Fluid', 'Rhinorrhea, CSF', 'Cerebrospinal fluid rhinorrhea', 'Cerebrospinal Fluid Rhinorrheas', 'Cerebrospinal Rhinorrheas', 'Rhinorrhea, Cerebrospinal Fluid, Traumatic', 'post Traumatic Rhinorrhea, Cerebrospinal Fluid', 'Cerebrospinal Fluid Rhinorrhea, post-Traumatic', 'Spontaneous Cerebrospinal Fluid Rhinorrhea', 'Cerebrospinal Fluid Rhinorrhea, Traumatic', 'Cerebrospinal Fluid Rhinorrhea', 'Rhinorrhea, Cerebrospinal Fluid, post-Traumatic', 'Cerebrospinal Rhinorrhea', 'post-Traumatic Rhinorrhea, Cerebrospinal Fluid', 'CSF Rhinorrhea']",,,,C0007815,,C84627,,D002559,349.81,,,0030998
mondo:0020774,Menke-Hennekam syndrome,,,,592574,,,,,,,,,
mondo:0020775,congenital disorder of glycosylation with defective fucosylation 1,"['CDGF1', 'Cdgf', 'CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 1']",,618005,,,,,,,,,,
mondo:0020776,chlamydiaceae infections,"['Infection, Chlamydiaceae', 'Chlamydiaceae Infection', 'Chlamydiaceae Infections', 'Infections, Chlamydiaceae']",,,,C0008153,,,1001288,D002694,,,,
mondo:0020777,congenital disorder of glycosylation with defective fucosylation 2,"['CONGENITAL DISORDER OF GLYCOSYLATION WITH DEFECTIVE FUCOSYLATION 2', 'CDGF2']",,618324,,,,,,,,,,
mondo:0020778,cone-rod dystrophy and hearing loss 1,"['Crdhl', 'cone-rod dystrophy and hearing loss', 'CRDHL1', 'CONE-ROD DYSTROPHY AND HEARING LOSS 1']",,617236,,,,,,,,,,
mondo:0020779,cartilage development disorder,"['Congenital anomaly of cartilage', 'abnormal development of cartilage', 'cartilage development disorder', 'chondrodystrophy']",,,,C0008449,,C34466,,,756.9,,,
mondo:0020780,cone-rod dystrophy and hearing loss 2,"['CRDHL2', 'CONE-ROD DYSTROPHY AND HEARING LOSS 2']",,618358,,,,,,,,,,
mondo:0020781,"encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy, 1","['PEBEL1', 'ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY, 1', 'encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy', 'encephalopathy, progressive, early-onset, with brain oedema and/or leukoencephalopathy', 'NAD(P)HX epimerase deficiency']",,617186,555407,,"['-0.0763', '0.294', '-0.2072', '-0.2397', '-0.3652', '-0.43', '0.0382', '0.4363', '-0.4978', '0.298', '-0.5317', '-0.2035', '-0.3696', '-0.09503', '0.356', '-0.234', '0.1384', '-0.2769', '-0.1635', '-0.6187', '0.1466', '-0.2915', '-0.0556', '-0.4333', '-0.00915', '-0.355', '-0.08795', '0.1608', '-0.684', '-0.005535', '0.01028', '0.11914', '0.261', '-0.08264', '0.0004177', '0.2325', '-0.3176', '0.04492', '-0.08075', '-0.05878', '0.000789', '-0.4824', '0.1046', '0.1979', '-0.0765', '-0.02245', '-0.3984', '0.0368', '-0.2416', '0.1765', '0.06015', '0.3801', '-0.1051', '-0.02255', '0.0962', '-0.01273', '0.3281', '-0.08984', '-0.1906', '0.3232', '0.05963', '0.0683', '0.01311', '0.0937', '-0.4292', '-0.0878', '0.526', '0.569', '-0.2263', '0.4382', '-0.156', '0.3665', '-0.1501', '-0.3206', '-0.05777', '-0.157', '0.4263', '0.1455', '-0.07086', '-0.1644', '-0.1317', '-0.1497', '-0.08887', '0.4463', '0.05695', '0.1085', '0.275', '0.4602', '0.3457', '0.1493', '0.5615', '0.4922', '-0.0404', '0.2869', '0.084', '0.2654', '0.4324', '0.05106', '0.4463', '0.1349']",,0009158,,,,,
mondo:0020782,chronic gingivitis,"['Chronic gingivitis', 'chronic gingivitis', 'Chronic Gingivitis']",,,,C0008684,,C34474,,,523.10,,,
mondo:0020783,capillary malformation-arteriovenous malformation 1,"['CMAVM1', 'CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 1', 'PKWS', 'Parkes Weber syndrome', 'Capillary Malformation-Arteriovenous Malformation']",,608355,90307,CN206396,,,,,759.6,,,
mondo:0020785,capillary malformation-arteriovenous malformation 2,"['CMAVM2', 'CAPILLARY MALFORMATION-ARTERIOVENOUS MALFORMATION 2']",,618196,,,,,,,,,,
mondo:0020787,"hypomagnesemia, seizures, and intellectual disability 1","['hypomagnesemia, seizures, and mental retardation', 'HOMGSMR1', 'HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 1']",,616418,,,,,,,,,,
mondo:0020788,"hypomagnesemia, seizures, and intellectual disability 2","['HYPOMAGNESEMIA, SEIZURES, AND MENTAL RETARDATION 2', 'HOMGSMR2']",,618314,,,,,,,,,,
mondo:0020789,pseudo-TORCH syndrome 1,"['pseudo-TORCH syndrome', 'pseudo-TORCH syndrome type 1', 'PTORCH1', 'pseudo-TORCH syndrome 1']",,251290,,,,,,,,,,
mondo:0020790,"gaze palsy, familial horizontal, with progressive scoliosis 1","['Ophthalmoplegia, Progressive External, and Scoliosis', 'HGPPS1', 'gaze palsy, familial horizontal, with progressive scoliosis, 1', 'HGPPS', 'gaze palsy, familial horizontal, with progressive scoliosis 1']",,607313,,,,,,,,,,
mondo:0020791,"corneal dystrophy, Meesmann, 1","['Meesmann Corneal Dystrophy', 'Corneal Dystrophy, Meesmann Epithelial', 'Corneal Dystrophy, Juvenile Epithelial, of Meesmann', 'MECD1', 'CORNEAL DYSTROPHY, MEESMANN, 1', 'meesmann corneal dystrophy 1']",0080670,122100,,,,,,,,,,
mondo:0020792,dwarfism with tall vertebrae,,,126950,,,,,,C535725,,,,
mondo:0020793,oculopharyngodistal myopathy 1,"['oculopharyngodistal myopathy 1', 'oculopharyngodistal myopathy', 'OPDM1', 'faciooculolaryngopharyngeal myopathy with distal and respiratory involvement']",0081297,164310,,,,,,,,,,
mondo:0020794,colorectal medullary carcinoma,['colorectal medullary carcinoma'],,,,,,C43590,,,,,,
mondo:0020795,Silver-Russell syndrome 5,"['SILVER-RUSSELL SYNDROME 5', 'SRS5']",,618908,,,,,,,,,,
mondo:0020796,Silver-Russell syndrome 1,['SRS1'],,180860,,,,,,,,,,
mondo:0020797,decompression sickness,"['Decompression sickness', 'Divers^ palsy', 'Divers^ paralysis', 'Bends', 'Caisson disease', 'Disease, Caisson', 'The bends', 'Compressed air disease', 'Decompression Sickness', 'Rapture of the deep syndrome', 'Caisson Disease', 'Caisson Diseases', 'CAISSON DIS', 'Compressed-air disease', 'Sickness, Decompression', 'Diseases, Caisson']",,,,C0011119,,,,D003665,993.3,,,
mondo:0020798,"hypoparathyroidism, familial isolated, 2","['hypoparathyroidism, familial isolated 2', 'FIH2', 'hypoparathyroidism, familial isolated, 2']",,618883,,,,,,,,,,
mondo:0020799,basal cell neoplasm,"['basal cell tumor', 'neoplasm, basal cell', 'basal cell tumour']",,,,,,C3784,,D018295,,,,
mondo:0020800,demyelinating disease of central nervous system,"['demyelinating disorder of central nervous system', 'demyelinating disease of central nervous system', 'demyelinating disease central nervous system (CNS)', 'demyelinating CNS disease', 'demyelinating disorders of the central nervous system']",,,,C0011302,,C34526,,,341.9,G35-G37,,
mondo:0020801,rectal medullary carcinoma,['rectal medullary carcinoma'],,,,,,C60640,,,,,,
mondo:0020804,basal cell carcinoma,"['epithelioma, basal cell', 'malignant basal cell neoplasm']",,,,,,C7586,,D002280,,,,
mondo:0020805,benign basal cell neoplasm,['benign basal cell tumour'],,,,,,C4743,,,,,,
mondo:0020806,sinoatrial block,,,,,,,,,D012848,,,,
mondo:0020807,ovarian sertoli-stromal cell tumor,"['Ovarian Sertoli-Stromal Tumor', 'Ovarian Sertoli-Stromal Cell Tumour', 'Ovarian Sertoli-Stromal Cell Tumor', 'Ovarian Sertoli-Stromal Tumour']",,,,,,C39966,,,,,,
mondo:0020808,testicular sertoli cell tumor,"['Sertoli Cell Tumour of Testis', 'Testicular Sertoli Cell Tumour', 'Sertoli Cell Tumour of the Testis']",,,,,,C4672,,,,,,
mondo:0020809,benign sertoli cell tumor,['Benign Sertoli Cell Tumour'],,,,,,C67012,,,,,,
mondo:0020811,"mitochondrial complex III deficiency, nuclear type",,,,,,,,,,,,,
mondo:0020812,"exposure, dental pulp","['Pulp Exposure, Dental', 'Dental Pulp Exposure', 'PULP EXPOSURE DENT', 'Exposure of tooth pulp', 'EXPOSURE DENT PULP', 'DENT PULP EXPOSURE', 'Exposure, Dental Pulp']",,,,C0011406,,,1001782,D003789,,,,
mondo:0020813,benign testicular sertoli cell tumor,"['benign testicular sertoli cell tumor', 'benign sertoli cell tumour of testis', 'benign sertoli cell tumour of the testis', 'benign sertoli cell neoplasm of the testis', 'benign testicular sertoli cell neoplasm', 'benign sertoli cell tumor of the testis', 'benign sertoli cell neoplasm of testis', 'benign sertoli cell tumor of testis']",,,,,,C6522,,,,,,
mondo:0020814,miliaria alba,,,,,,,,,,,,,
mondo:0020815,dentigerous cyst,"['Dentigerous odontogenic cyst', 'Dentigerous cyst of jaw', 'Dentigerous Cyst', 'Cysts, Dentigerous', 'Cyst, Dentigerous', 'Dentigerous Cysts', 'Dentigerous cyst']",,,,C0011428,,,,D003803,,,,
mondo:0020816,miliaria papulosa,,,,,,,,,,,,,
mondo:0020817,miliaria vesiculosa,,,,,,,,,,,,,
mondo:0020818,secondary dentine,"['Secondary dentine', 'Reparative dentine', 'Irregular dentine', 'Secondary Dentins', 'Dentins, Secondary', 'Dentin, Secondary', 'Secondary dentin', 'Secondary Dentin', 'SECOND DENTIN', 'DENTIN SECOND', 'Sclerotic dentine', 'Tertiary dentine', 'Irregular dentin']",,,,C0011434,,,,D003809,,,,
mondo:0020820,distal arthrogryposis type 2B1,"['DA2B1', 'arthrogryposis, distal, type 2B1']",0111600,601680,,,,,,,,,,
mondo:0020823,infantile miliaria,,,,,,,,,,,,,
mondo:0020830,diaphragmitis,"['diaphragmitis', 'diaphragmatitis']",,,,C0011985,,,0000937,,,,,
mondo:0020831,congenital vertebral-cardiac-renal anomalies syndrome,"['vertebral, cardiac, renal, and limb defects syndrome', 'VCRL']",,,521438,,"['-0.1653', '-0.0782', '0.5684', '-0.3733', '0.1702', '-0.2598', '0.07336', '0.547', '-0.1311', '-0.1304', '-0.0521', '-0.255', '-0.1733', '0.02255', '-0.5425', '-0.2556', '-0.2773', '0.07666', '-0.2039', '-0.443', '0.265', '0.292', '0.0725', '-0.1633', '0.2062', '-0.10876', '-0.1494', '0.1499', '0.4905', '-0.127', '0.3352', '-0.07996', '0.599', '0.3315', '0.209', '-0.498', '-0.1017', '-0.2324', '-0.1582', '-0.1602', '0.03525', '0.01808', '0.1043', '-0.07166', '-0.05545', '-0.2062', '-0.01567', '0.4622', '-0.3027', '0.12384', '-0.318', '0.175', '0.1261', '-0.2622', '-0.384', '-0.303', '-0.1473', '-0.05765', '-0.2261', '-0.02206', '0.1598', '0.049', '-0.227', '0.05804', '-0.1461', '-0.2766', '0.2078', '0.591', '-0.4553', '0.1464', '-0.3977', '0.0804', '0.0986', '-0.1323', '-0.1282', '-0.1073', '0.2102', '-0.1432', '-0.3772', '-0.0674', '0.11426', '0.1531', '-0.12146', '0.3877', '-0.01878', '-0.058', '0.1793', '0.2421', '0.06247', '0.194', '0.188', '0.3184', '0.1772', '0.06775', '0.7686', '-0.0313', '0.592', '-0.2347', '0.2106', '0.4675']",,,,,,,
mondo:0020835,"methemoglobinemia, alpha type","['methemoglobinemia, alpha type']",,617973,,,,,,,,,,
mondo:0020836,"autism, susceptiblity to",,,,,,,,,,,,,
mondo:0020837,oocyte maturation defect 5,"['oocyte maturation defect 5', 'OOMD5']",,617996,,,,,,,,,,
mondo:0020838,anterior nasal diphtheria,"['Anterior Nasal Diphtheria', 'anterior nasal diphtheria', 'Anterior nasal diphtheria']",,,,C0012553,,C34542,,,032.2,,,
mondo:0020840,pulmonary alveolar proteinosis with hypogammaglobulinemia,"['pulmonary alveolar proteinosis with hypogammaglobulinemia', 'immunodeficiency (due to OAS1 gain-of-function variant) with pulmonary alveolar proteinosis and hypogammaglobulinemia', 'PAPHG']",,618042,,CN248786,,,,,,,,
mondo:0020841,neurodevelopmental disorder with cerebellar atrophy and with or without seizures,"['neurodevelopmental disorder with cerebellar atrophy and with or without seizures', 'NEDCAS']",,618056,,CN252657,"['-0.06586', '0.0815', '0.02927', '-0.06058', '0.008644', '-0.1482', '0.02013', '0.1765', '-0.1779', '-0.0617', '-0.06415', '-0.0726', '-0.05783', '-0.02457', '-0.00536', '-0.08325', '0.02298', '-0.0956', '-0.0701', '-0.2668', '0.01173', '-0.06134', '0.06354', '-0.04272', '0.0635', '-0.0767', '0.01408', '-0.03394', '0.03705', '-0.06616', '0.04416', '-0.03006', '0.1655', '0.02376', '0.006287', '0.001913', '-0.1196', '-0.04855', '-0.04843', '-0.1248', '0.05515', '-0.158', '0.01359', '0.011345', '-0.02', '-0.1582', '-0.03207', '0.09283', '-0.04913', '0.0443', '-0.01968', '0.0662', '0.003462', '0.003647', '-0.003061', '-0.004826', '0.09985', '-0.0717', '-0.1857', '0.0533', '0.0351', '0.069', '0.0539', '0.02539', '-0.0916', '0.006084', '0.1334', '0.09796', '-0.05975', '0.1221', '-0.11975', '0.08203', '0.02544', '-0.1084', '0.04755', '0.0646', '0.0625', '-0.03522', '-0.06696', '-0.02162', '0.01569', '0.02832', '-0.0279', '0.158', '0.002905', '0.01544', '0.005135', '0.1625', '0.1292', '0.04218', '0.04056', '0.1583', '-0.00571', '0.04977', '0.2092', '0.0983', '0.1183', '-0.10455', '0.0003064', '0.08954']",,,,,,,
mondo:0020843,pseudomembranous diphtheritic conjunctivitis,"['pseudomembranous diphtheritic conjunctivitis', 'Conjunctival diphtheria']",,,,C0012554,,C34543,,,032.81,,,
mondo:0020845,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5","['progressive external ophthalmoplegia, autosomal recessive 5', 'PEOB5', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 5']",0111524,618098,,,"['-0.1142', '0.1361', '-0.01642', '-0.01607', '0.0937', '-0.1819', '0.0239', '0.1476', '-0.1699', '-0.08716', '-0.00811', '-0.01799', '0.0589', '0.0085', '-0.02348', '-0.05695', '-0.00395', '-0.05594', '-0.0833', '-0.1871', '-0.05615', '-0.06274', '0.06113', '-0.01631', '0.04276', '0.00537', '-0.05725', '-0.02432', '-0.02502', '-0.07166', '0.0917', '0.02937', '0.1495', '0.00428', '-0.01231', '-0.1296', '-0.06946', '-0.085', '-0.03317', '-0.103', '0.0687', '-0.1764', '0.01058', '0.04434', '-0.05847', '-0.1619', '-0.04114', '0.04587', '0.0791', '-0.00785', '-0.04855', '-0.02246', '-0.01252', '-0.005005', '-0.04388', '-0.1284', '0.1727', '-0.04523', '-0.1482', '0.0238', '0.1182', '0.01996', '0.0564', '0.02701', '-0.05692', '0.000992', '0.1272', '0.1251', '-0.1051', '0.1755', '-0.1176', '-0.01413', '0.06946', '-0.04706', '0.09607', '0.08', '0.002666', '0.02275', '-0.11035', '-0.04813', '0.002256', '0.04074', '0.011375', '0.11804', '-0.0503', '0.0466', '0.0766', '0.141', '0.09515', '0.04538', '0.0733', '0.1476', '-0.01097', '-0.01419', '0.2424', '0.09576', '0.1653', '-0.1423', '-0.03668', '0.03287']",,,,,,,
mondo:0020846,"intellectual disability, autosomal recessive 64","['MRT64', 'MENTAL RETARDATION, autosomal recessive 64']",0081225,618103,,,"['-0.04422', '0.09033', '0.01534', '-0.03003', '0.02861', '-0.1009', '-0.01982', '0.1003', '-0.0627', '-0.0642', '-0.03305', '0.02113', '0.01307', '0.006893', '-0.01459', '-0.02908', '0.01099', '-0.02385', '-0.03546', '-0.1313', '-0.0348', '-0.01118', '0.04227', '-0.0427', '0.0399', '-0.009544', '-0.0295', '-0.01593', '0.02069', '-0.0633', '0.06995', '0.00227', '0.0839', '0.02295', '-0.01581', '-0.0162', '-0.02412', '-0.06168', '-0.0175', '-0.08325', '0.0378', '-0.0888', '0.02824', '-0.03345', '-0.012856', '-0.0897', '-0.011925', '0.03918', '0.02327', '0.0343', '0.001056', '-0.004', '0.000954', '-0.01839', '-0.001624', '-0.0636', '0.0862', '-0.01016', '-0.1219', '0.01869', '0.03732', '0.01463', '0.01081', '0.01031', '-0.00781', '0.004505', '0.0886', '0.06744', '-0.0894', '0.0633', '-0.07355', '0.01493', '0.0366', '-0.06946', '0.0498', '0.07117', '0.02724', '-0.02461', '-0.03568', '-0.03207', '0.005116', '0.01391', '-0.01845', '0.0804', '0.010605', '0.01787', '0.03683', '0.09607', '0.0943', '0.03128', '0.0414', '0.09894', '-0.01164', '0.0238', '0.1614', '0.05832', '0.06476', '-0.1071', '0.01401', '0.0365']",,,,,,,
mondo:0020847,"intellectual disability, autosomal dominant 58","['MRD58', 'MENTAL RETARDATION, autosomal dominant 58']",,618106,,,"['-0.01941', '0.02037', '0.01336', '-0.00967', '-0.001342', '-0.01839', '-0.004436', '0.02074', '-0.02986', '-0.0118', '-0.0003889', '-0.000844', '0.006786', '0.00585', '0.004837', '-0.00854', '-0.000858', '-0.00721', '-0.001884', '-0.04776', '-0.00974', '0.002333', '0.01917', '-0.00979', '0.001217', '0.00294', '0.0003295', '9.43e-05', '0.001201', '-0.01163', '0.02846', '-0.003735', '0.02829', '0.005222', '0.003511', '-0.001436', '-0.01403', '-0.01602', '-0.004673', '-0.02124', '0.01608', '-0.03128', '0.00317', '0.001986', '-0.005775', '-0.029', '-0.003393', '0.0197', '0.002493', '0.00783', '-0.00992', '0.0003424', '-0.0004208', '-0.0008616', '0.0001556', '-0.01918', '0.02902', '-0.00561', '-0.0272', '0.01088', '0.01761', '0.011856', '-0.009995', '0.00934', '0.00538', '0.00365', '0.0253', '0.02803', '-0.02832', '0.02559', '-0.01294', '0.006966', '0.005802', '-0.012634', '0.01228', '0.008606', '0.01264', '0.003696', '-0.01671', '-0.02055', '0.008644', '0.0086', '-0.006508', '0.01308', '0.00747', '-0.00237', '0.003906', '0.01435', '0.03247', '0.001196', '0.01056', '0.01807', '0.003693', '0.0099', '0.034', '0.01723', '0.0216', '-0.03796', '-0.000157', '0.0207']",,,,,,,
mondo:0020848,"osteopetrosis, autosomal dominant 3","['OSTEOPETROSIS, autosomal dominant 3', 'OPTA3']",,618107,,,,,,,,,,
mondo:0020849,immunodeficiency 57,"['IMMUNODEFICIENCY 57', 'immunodeficiency 57 with autoinflammation', 'IMD57']",0111952,618108,,,,,,,,,,
mondo:0020850,"intellectual disability, autosomal recessive 65","['intellectual disability, autosomal recessive 65', 'MRT65', 'mental retardation, autosomal recessive 65']",0081226,618109,,,,,,,,,,
mondo:0020851,spermatogenic failure 30,"['SPGF30', 'spermatogenic failure 30']",0111913,618110,,,,,,,,,,
mondo:0020852,spermatogenic failure 31,"['spermatogenic failure 31', 'SPGF31']",0111922,618112,,,,,,,,,,
mondo:0020853,"encephalitis/encephalopathy, mild, with reversible myelin vacuolization","['Encephalitis/encephalopathy, mild, with reversible splenial lesion', 'MMERV', 'encephalitis/encephalopathy, mild, with reversible myelin vacuolization']",,618113,,,"['-0.10187', '0.04523', '0.0213', '-0.03108', '-0.07587', '-0.0787', '-0.0307', '0.08966', '-0.08093', '0.000831', '-0.0637', '0.02336', '-0.02882', '0.02312', '0.01058', '-0.082', '-0.0391', '-0.0636', '-0.05362', '-0.2042', '0.014465', '-0.0091', '0.05377', '0.02821', '0.04025', '-0.0809', '-0.02092', '-0.0115', '-0.04794', '-0.0581', '0.04163', '0.01388', '0.0776', '0.05618', '0.02374', '-0.04642', '-0.00784', '-0.01552', '0.00994', '-0.0691', '0.04315', '-0.0994', '0.0497', '-0.006012', '0.035', '-0.10297', '-0.02089', '0.0298', '0.04993', '0.06128', '0.00809', '-0.03165', '0.003286', '-0.00323', '-0.044', '0.01113', '0.1225', '-0.06793', '-0.1008', '0.03458', '0.02855', '0.04602', '0.03528', '0.00838', '-0.052', '-0.01502', '0.08435', '0.1996', '-0.03494', '0.1159', '-0.04187', '0.02785', '0.0728', '-0.08075', '0.02122', '0.05417', '0.05536', '0.04944', '-0.0414', '-0.06305', '-0.02127', '-0.03796', '-0.06097', '0.10065', '-0.00725', '-0.01523', '0.01442', '0.04828', '0.1486', '0.01979', '0.05576', '0.0916', '0.01347', '0.0467', '0.2068', '0.1173', '0.1147', '-0.146', '-0.001814', '0.03598']",,,,,,,
mondo:0020854,Liddle syndrome 2,"['LIDLS2', 'SCNN1G Liddle syndrome', 'Liddle syndrome 2']",,618114,,,"['-0.0261', '0.05847', '0.02078', '0.0008817', '0.02757', '-0.07947', '0.00989', '0.07166', '-0.05557', '-0.034', '-0.03415', '-0.02498', '0.02293', '0.0045', '-0.02623', '-0.0454', '-0.00645', '0.013054', '-0.006855', '-0.1118', '0.0091', '-0.0303', '0.07477', '-0.02771', '0.02132', '-0.01472', '-0.02045', '-0.02301', '0.015594', '-0.04742', '0.05774', '-0.00184', '0.0958', '0.04675', '-0.004803', '-0.0456', '0.0003133', '-0.03394', '-0.00727', '-0.0753', '0.02892', '-0.06396', '0.0142', '-0.03287', '-0.013855', '-0.06494', '-0.01764', '0.06934', '-0.000673', '0.0035', '-0.0261', '-0.02177', '0.000766', '-0.01572', '-0.02621', '-0.02621', '0.06305', '-0.03928', '-0.0788', '0.01672', '0.04648', '0.04358', '0.01366', '-0.0006776', '0.00886', '-0.004047', '0.0629', '0.04044', '-0.0815', '0.08246', '-0.07434', '0.005062', '0.02724', '-0.04285', '0.0526', '0.0315', '-0.01408', '-0.000824', '-0.07214', '-0.03864', '0.008575', '0.001155', '-0.01454', '0.05798', '-0.02776', '0.01231', '0.03543', '0.0894', '0.08545', '0.01695', '0.02751', '0.0602', '0.01537', '0.009186', '0.1371', '0.02414', '0.05618', '-0.1207', '-0.02608', '0.02936']",,,,,,,
mondo:0020855,spermatogenic failure 32,"['SPGF32', 'spermatogenic failure 32']",0111925,618115,,,,,,,,,,
mondo:0020856,bone marrow failure syndrome 4,"['BMFS4', 'BONE MARROW FAILURE SYNDROME 4']",,618116,,,,,,,,,,
mondo:0020857,ovarian dysgenesis 7,"['OVARIAN DYSGENESIS 7', 'ODG7']",0080499,618117,,,,,,,,,,
mondo:0020858,mitochondrial complex 5 (ATP synthase) deficiency nuclear type 5,"['Mitochondrial Complex 5 (ATP Synthase) Deficiency, ATP5F1D Type', 'mitochondrial complex v (atp synthase) deficiency', 'MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 5', 'MC5DN5']",,618120,,,,,,,,,,
mondo:0020860,faucial diphtheria,"['Faucial Diphtheria', 'Faucial diphtheria', 'Diphtheritic membrane', 'faucial diphtheria', 'Diphtheritic membranous angina']",,,,C0012556,,C34545,,,032.0,,,
mondo:0020863,laryngeal diphtheria,"['laryngeal diphtheria', 'Laryngeal diphtheria', 'Laryngeal Diphtheria', 'Diphtheritic laryngotracheitis']",,,,C0012557,,C34546,,,032.3,,,
mondo:0020866,nasopharyngeal diphtheria,"['nasopharyngeal diphtheria', 'Nasopharyngeal diphtheria', 'Nasopharyngeal Diphtheria']",,,,C0012558,,C34547,,,032.1,,,
mondo:0020920,escherichia coli infection,"['INFECT E COLI', 'E coli infections', 'Infection, Escherichia coli', 'E Coli Infection', 'E. coli Infection', 'Infection caused by Escherichia coli', 'Recurrent E. coli infections', 'E. coli infection', 'Infection due to Escherichia coli', 'E coli Infection', 'E coli Infections', 'Bacterial infection due to E. coli', 'Escherichia coli infection', 'Escherichia Coli Infection', 'ESCHERICHIA COLI INFECT', 'E COLI INFECT', 'Infection, E. coli', 'INFECT ESCHERICHIA COLI', 'Infection, E coli', 'E. coli Infections', 'Infections, E coli', 'escherichia coli infection', 'Colibacillosis', 'e coli infection', 'Escherichia coli Infections', 'E coli infections, recurrent', 'Bacterial infection caused by E. coli', 'Infections, Escherichia coli', 'Escherichia coli Infection']",,,,C0014836,,C34594,1001318,D004927,,,,0002740
mondo:0020927,postaxial polydactyly,,,,,,,,,,,,,
mondo:0020937,"contractures, pterygia, and variable skeletal fusions syndrome",,,,,,,,,,,,,
mondo:0020944,fungal infection of eye,"['Mycotic Infections, Ocular', 'Fungal Eye Infections', 'Mycoses, Ocular', 'OCULAR INFECT FUNGAL', 'Infection, Fungal Ocular', 'Ocular Infections, Fungal', 'Ocular Mycosis', 'Mycotic Infection, Ocular', 'Fungal Ocular Infection', 'Mycosis, Ocular', 'Ocular Mycotic Infections', 'Oculomycosis', 'Fungal Eye Infection', 'Fungal Ocular Infections', 'Ocular Infection, Fungal', 'Infection, Ocular Mycotic', 'Eye Infections, Fungal', 'Infections, Fungal Ocular', 'Eye Infection, Fungal', 'Oculomycoses', 'Fungal eye infection', 'Infection, Fungal Eye', 'Infections, Ocular Mycotic', 'Infections, Fungal Eye', 'Fungal infection of eye', 'FUNGAL EYE INFECT', 'MYCOTIC INFECT OCULAR', 'Ocular Mycotic Infection', 'EYE INFECT FUNGAL', 'Ocular mycosis', 'Ocular Mycoses']",,,,C0015405,,,,D015821,117.9,,,
mondo:0020947,parasitic eye infection,"['Infection, Parasitic Eye', 'Parasitic Eye Infection', 'Parasitic Ocular Infection', 'Infections, Parasitic Ocular', 'Eye Infection, Parasitic', 'OCULAR INFECT PARASITIC', 'Parasitic Eye Infections', 'Parasitic eye infection', 'Infections, Parasitic Eye', 'Parasitic Ocular Infections', 'Ocular Infection, Parasitic', 'Ocular Infections, Parasitic', 'Eye Infections, Parasitic', 'PARASITIC EYE INFECT', 'EYE INFECT PARASITIC', 'Infection, Parasitic Ocular']",,,,C0015406,,,,D015822,136.9,,,
mondo:0020950,viral eye infection,"['Viral eye infection', 'OCULAR INFECT VIRAL', 'EYE INFECT VIRAL', 'Ocular Infections, Viral', 'Infections, Viral Ocular', 'VIRAL EYE INFECT', 'Ocular Infection, Viral', 'Eye Infections, Viral', 'Viral Ocular Infections', 'Infection, Viral Ocular', 'Viral Eye Infections', 'Infection, Viral Eye', 'Infections, Viral Eye', 'Eye Infection, Viral', 'Viral Ocular Infection', 'Viral Eye Infection']",,,,C0015407,,,,D015828,,,,
mondo:0020959,Mansonella ozzardi infection,"['Filariasis ozzardi', 'mansonella ozzardi infection', 'Ozzardian filariasis']",,,,C0016089,,C34612,,,125.5,,,
mondo:0020971,gonococcal urethritis,"['gonococcal urethritis', 'gc urethritis', 'Gonococcal urethritis']",,,,C0018078,,C26787,,,,,,
mondo:0020974,laryngeal granuloma,"['Laryngeal granuloma', 'Laryngeal Granulomas', 'Laryngeal Granuloma', 'Granulomas, Laryngeal', 'Larynx Granuloma', 'Granuloma, Laryngeal', 'Larynx Granulomas', 'Granuloma of Larynx']",,,,C0018196,,,,D006102,478.79,,,
mondo:0020977,granulomatous prostatitis,"['Granulomatous prostatitis', 'granulomatous prostatitis', 'Granulomatous Prostatitis']",,,,C0018204,,C26789,,,601.8,,,
mondo:0020979,pilosebaceous hamartoma,['pilosebaceous hamartoma'],,,,,,C5565,,,,,,
mondo:0020980,hair nevus,"['nevoid hypertrichosis', 'hair nevus', 'hairy nevus']",,,,C0018508,,C3074,,,,,,
mondo:0020983,myocardial rupture,"['Rupture of heart', 'Cardiac Rupture', 'Cardiac Ruptures', 'Ventricular Free Wall Rupture', 'Cardiac Free Wall Rupture', 'Myocardial Rupture', 'Free Wall Rupture, Heart', 'Heart Rupture', 'Heart Ruptures']",,,,C0018813,,,,D006341,,,,
mondo:0020989,hereditary persistence of fetal hemoglobin,"['Disease, Hemoglobin F', 'Hb F disease', 'Hereditary Persistence of Foetal Haemoglobin', 'Hereditary persistence of foetal haemoglobin', 'Hereditary Persistence of Fetal Hemoglobin', 'Hemoglobin F Disease', 'HPFH - Hereditary persistence of fetal hemoglobin', 'Hereditary persistence of fetal hemoglobin', 'HEREDITARY PERSISTENCE of FETAL HEMOGLOBIN', 'Disease, Haemoglobin F', 'hereditary persistence of fetal hemoglobin', 'Haemoglobin F Disease', 'HPFH - Hereditary persistence of foetal haemoglobin', 'HEMOGLOBIN F DIS']",,142250,,C0019025,,C129072,,,282.7,,,
mondo:0021001,hemochromatosis type 1,"['HFE1', 'symptomatic form of classic hemochromatosis', 'symptomatic form of HFE-related hereditary hemochromatosis', 'HFE-associated hereditary hemochromatosis', 'C282Y/C282Y hemochromatosis', 'HFE-related hemochromatosis', 'hfe hemochromatosis, modifier of', 'hemochromatosis', 'symptomatic form of hemochromatosis type 1', 'hemochromatosis, type 1', 'classic hemochromatosis']",0111029,235200,465508,CN242134,"['0.218', '0.4053', '-0.4736', '-0.06696', '0.6104', '0.00979', '-0.6807', '0.467', '0.2225', '-0.027', '0.2191', '0.2308', '-0.4836', '0.4592', '-0.667', '-0.1487', '-0.3667', '0.1757', '-0.5474', '-0.849', '-0.434', '-0.5054', '0.575', '-0.352', '0.4714', '0.0802', '0.1844', '-0.0227', '0.1744', '0.05637', '0.902', '-0.9243', '0.5815', '0.0838', '-0.1779', '-0.3704', '-0.9785', '-0.063', '0.2487', '0.1686', '0.5547', '-0.2343', '-0.009445', '0.518', '0.282', '-0.911', '-0.00499', '-0.7334', '0.05246', '-0.04178', '0.07806', '0.0609', '0.594', '0.0783', '0.529', '-0.3906', '0.1934', '0.4739', '-0.1459', '-0.07635', '0.6', '0.5264', '0.6426', '-0.2177', '-0.0354', '0.302', '-0.322', '0.5273', '-0.728', '-0.2686', '0.128', '0.532', '0.3794', '-0.2449', '0.03632', '0.02275', '0.01414', '0.7773', '-0.012566', '0.3606', '0.11255', '-0.5635', '-0.2576', '-0.458', '-0.0549', '-0.4116', '0.8394', '0.139', '0.5615', '-0.08734', '0.979', '0.2064', '-0.3542', '-0.4043', '0.6724', '0.707', '0.0605', '-0.377', '-0.128', '0.1663']",C84764,0006513,,275.01,,,
mondo:0021002,syndactyly,['syndactyly (disease)'],11193,,,C0039075,,,,D013576,755.1,,10042778,0001159
mondo:0021003,polydactyly,"['polydactyly (disease)', 'polydactyly', 'postaxial polydactyly', 'supernumerary digit', 'polydactylism', 'hyperdactyly']",1148,603596,,,,C87110,,D017689,755.00,,10036063,0010442
mondo:0021004,brachydactyly,"['brachydactyly', 'brachydactyly (disease)']",0050581,,,,,,,D059327,,,,0001156
mondo:0021005,faciodigitogenital syndrome,,0111824,,915,,,,,,,,10067148,
mondo:0021008,secondary antiphospholipid syndrome,,,,,C0409983,,,,,795.79,,,
mondo:0021009,salivary gland mucoepidermoid carcinoma,"['mucoepidermoid carcinoma of the salivary gland', 'mucoepidermoid carcinoma of salivary gland', 'salivary gland mucoepidermoid carcinoma', 'saliva-secreting gland mucoepidermoid carcinoma']",0081293,,,C1335903,,C5908,,,,,,
mondo:0021010,skin lymphangiosarcoma,"['lymphangiosarcoma of skin', 'lymphangiosarcoma of Stewart and Treves', 'skin lymphangiosarcoma', 'lymphangiosarcoma of the skin']",,,,C0346082,,C4490,,,171.2,,,
mondo:0021011,hereditary progressive chorea without dementia,"['BCH', 'chorea, benign hereditary', 'BHC', 'hereditary progressive chorea without dementia', 'chorea, hereditary benign']",,118700,,,,,,,,,,
mondo:0021012,"susceptibility to visceral leishmaniasis, 1","['kala-Azar, susceptibility to, 1', 'leishmaniasis, visceral, susceptibility to, 1', 'KAZA1']",,608207,,,,,,,,,,
mondo:0021013,"trichothiodystrophy 4, nonphotosensitive","['trichothiodystrophy-neurocutaneous syndrome', 'trichothiodystrophy, nonphotosensitive 1', 'Amish brittle hair brain syndrome', 'nonphotosensitive trichothiodystrophy caused by mutation in MPLKIP', 'trichothiodystrophy 4, nonphotosensitive', 'Pollitt syndrome', 'hair-brain syndrome', 'nonphotosensitive trichothiodystrophy', 'BIDS syndrome', 'MPLKIP nonphotosensitive trichothiodystrophy', 'TTD4']",0050528,234050,75790,,,C146899,,,783.43,,,
mondo:0021017,synaptopathy,,,,,,,,,,,,,
mondo:0021018,autosomal dominant limb-girdle muscular dystrophy type 1D (DNAJB6),"['LGMD1E', 'muscular dystrophy limb-girdle type 1D', 'muscular dystrophy, limb-girdle, type 1D, formerly', 'LGMD1D (DNAJB6)', 'autosomal dominant limb-girdle muscular dystrophy type 1E', 'autosomal dominant limb-girdle muscular dystrophy caused by mutation in DNAJB6', 'muscular dystrophy, limb-girdle, type 1D', 'muscular dystrophy, limb-girdle, type 1E', 'LGMD1E (Bushby and Beckmann, 2003)', 'autosomal dominant limb-girdle muscular dystrophy type 1D', 'muscular dystrophy, limb-girdle, autosomal dominant 1', 'DNAJB6 autosomal dominant limb-girdle muscular dystrophy', 'muscular dystrophy limb-girdle type 1E', 'limb-girdle muscular dystrophy type 1D', 'LGMD1D']",0110305,603511,34516,C3501858,"['-0.08026', '-0.895', '-0.7188', '-0.4033', '0.5093', '-1.17', '-0.004345', '0.796', '-1.981', '-1.006', '-0.2554', '0.45', '-0.2688', '0.891', '0.3801', '0.3872', '-0.4888', '-0.4854', '-0.7124', '-0.698', '-0.04312', '0.09296', '0.512', '0.614', '0.257', '0.04175', '0.0903', '-0.919', '0.3057', '-0.3647', '0.9453', '-0.0006237', '0.5903', '0.1638', '0.04144', '-0.15', '-0.3718', '0.257', '0.1538', '-0.4646', '0.2335', '-0.3372', '-0.3015', '0.4307', '-0.1339', '0.0994', '-0.0701', '0.79', '-0.1376', '0.556', '0.5483', '-0.281', '0.2559', '-0.904', '0.19', '-0.5723', '0.5493', '0.7617', '-0.3516', '0.07965', '0.1082', '-0.1256', '-0.1715', '-0.1984', '-0.0866', '-0.2058', '0.1273', '0.3872', '-0.5327', '-0.4614', '-0.2654', '0.4094', '0.2656', '-0.1061', '0.6113', '0.5664', '0.188', '0.4133', '0.293', '0.2517', '0.08997', '-0.2064', '0.06134', '-0.0902', '-0.285', '0.2302', '-0.0999', '-0.1305', '1.058', '0.5483', '-0.3994', '0.05667', '0.388', '0.752', '-0.1345', '0.1614', '0.2625', '-0.5225', '-0.1628', '-0.1438']",,,C566370,,,,
mondo:0021019,X-linked recessive ocular albinism,"['OA1', 'ocular albinism, Nettleship-Falls type', 'albinism, ocular, type 1', 'X-linked ocular albinism', 'Nettleship-Falls type ocular albinism', 'Nettleship-Falls syndrome', 'albinism, ocular, type I', 'ocular albinism, type I, Nettleship-Falls type', 'ocular albinism type 1', 'XLOA']",,300500,54,C0342684,"['0.2365', '0.1417', '-0.2162', '0.1417', '0.5356', '0.1752', '-0.295', '0.557', '-0.3872', '-0.568', '0.43', '-0.228', '0.2444', '1.176', '-0.1903', '0.472', '0.547', '0.0811', '0.4338', '-0.507', '-0.9575', '-0.0881', '0.5854', '-0.4321', '-0.2517', '-0.2258', '-0.7397', '-0.1941', '0.6426', '0.1863', '0.3494', '0.05682', '0.09216', '0.5137', '0.0972', '0.4248', '-0.775', '-0.642', '0.2046', '-0.3933', '1.295', '-0.1343', '-0.359', '0.04443', '-0.1959', '-0.618', '0.4478', '-0.849', '0.861', '0.4475', '-0.2935', '-0.4487', '0.1954', '-0.2656', '0.4292', '0.2352', '0.4036', '0.999', '-0.0903', '-0.884', '-0.2822', '0.08527', '0.388', '0.4558', '-0.1558', '0.3433', '0.1732', '0.562', '-0.381', '0.5566', '0.01188', '0.3623', '0.0986', '-0.1661', '0.8354', '0.162', '0.1528', '-0.2136', '0.07886', '-0.2534', '0.774', '-0.581', '0.5723', '0.5537', '-0.367', '-1.235', '0.327', '0.496', '0.8716', '0.2314', '0.1669', '1.028', '-0.12054', '-0.2369', '0.4805', '0.1649', '-0.3572', '-0.5283', '0.2473', '0.337']",C118785,,C537863,270.2,,,
mondo:0021020,Crigler-Najjar syndrome type 1,"['Crigler-Najjar syndrome, type I', 'hyperbilirubinemia, Crigler-Najjar type 1', 'UGT deficiency type 1', 'Crigler Najjar syndrome, type 1', 'bilirubin uridinediphosphate glucuronosyltransferase deficiency type 1', 'hereditary unconjugated hyperbilirubinemia type 1', 'Crigler-Najjar syndrome, type 1', 'bilirubin-UGT deficiency type 1']",,218800,79234,,"['0.5024', '0.2969', '-0.1004', '-0.1677', '-0.275', '0.2983', '-0.0889', '0.3513', '-0.2656', '-0.226', '-0.183', '-0.106', '0.03053', '0.02528', '-0.2462', '-0.3528', '0.0633', '-0.1543', '-0.0445', '-1.158', '-0.0058', '-0.2422', '0.5034', '-0.01659', '-0.2507', '-0.2428', '-0.02135', '0.2498', '-0.501', '0.2036', '-0.236', '0.5938', '0.03473', '0.2429', '-0.689', '-0.01604', '0.11206', '-0.641', '0.1763', '0.4272', '0.2341', '-0.6265', '0.4863', '0.0671', '-0.1224', '-0.2413', '-0.137', '-0.1244', '0.062', '0.1528', '0.5063', '-0.11536', '-0.1054', '-0.7607', '-0.3677', '0.6045', '0.1704', '0.3333', '-0.694', '0.4133', '0.1709', '0.557', '0.753', '-0.3403', '-0.0814', '0.003565', '0.348', '0.1327', '-0.5615', '0.08704', '-0.00783', '0.447', '0.1085', '-0.2372', '-0.1307', '0.2338', '0.939', '-0.2505', '-0.342', '-0.10223', '-0.1886', '0.4006', '-0.759', '0.3132', '-0.01854', '0.1819', '0.2703', '0.496', '0.2273', '0.04626', '0.8276', '0.3892', '-0.09357', '-0.5825', '0.383', '0.4705', '0.2576', '-0.4001', '-0.2163', '0.309']",,,,,,10057034,
mondo:0021021,"craniodiaphyseal dysplasia, autosomal dominant","['CDD', 'craniodiaphyseal dysplasia, dominant', 'Schaefer Stein Oshman syndrome', 'craniodiaphyseal dysplasia, autosomal dominant', 'dominantly inherited craniodiaphyseal dysplasia']",0080807,122860,,,,,,C567275,,,,
mondo:0021022,hereditary hyperekplexia,"['startle disease', 'Stiff baby syndrome', 'congenital stiff man syndrome', 'hyperexplexia hereditary', 'hyperekplexia', 'hereditary hyperekplexia', 'hereditary hyperexplexia', 'familial startle disease', 'Kok disease']",0060695,,3197,,"['-0.0318', '0.1278', '-0.4363', '-0.144', '-0.485', '-0.2362', '0.0713', '0.575', '-0.1472', '-0.06415', '-0.2554', '0.563', '0.461', '-0.2122', '0.4893', '0.3064', '0.3342', '-0.3306', '-0.1887', '-0.951', '0.2888', '0.00568', '-0.10547', '0.07935', '-0.2413', '-0.010864', '-0.896', '-0.2722', '-0.463', '-0.068', '0.3113', '-0.2378', '-0.1655', '-0.2727', '-0.0928', '-0.0116', '0.5938', '-0.3914', '-0.2021', '-0.1866', '0.01051', '-0.4365', '0.1161', '-0.003952', '-0.06094', '-0.4773', '0.03625', '0.3103', '0.1823', '1.485', '-0.03021', '-0.2595', '-0.2034', '0.1665', '0.3528', '-0.2432', '0.6216', '-0.2803', '0.3916', '0.752', '0.0569', '0.5127', '0.11414', '0.00901', '-0.0889', '0.2966', '0.2314', '0.8755', '-0.3337', '-0.3647', '-0.334', '0.4023', '0.2455', '-0.369', '0.869', '0.5786', '-0.654', '0.3328', '-0.386', '0.10614', '-0.382', '-0.03165', '0.02513', '0.02728', '-0.1831', '0.476', '-0.07904', '0.1719', '-0.3242', '0.457', '-0.1885', '-0.1735', '-0.5654', '0.1951', '0.1223', '0.724', '0.8247', '-0.5693', '-0.01055', '0.07623']",,,,,,,
mondo:0021023,complete androgen insensitivity syndrome,"['complete androgen resistance syndrome', 'CAIS', 'androgen insensitivity syndrome, complete']",0080775,,99429,CN207337,"['-0.05087', '-0.1121', '-0.3542', '-0.48', '0.725', '-0.2', '-0.4202', '1.178', '-0.278', '-0.1573', '0.1004', '0.3206', '0.0756', '0.6167', '-0.2712', '0.06354', '0.3909', '-0.09436', '-0.468', '-0.6055', '-0.716', '-0.2754', '0.8306', '-0.1181', '0.414', '-0.1776', '0.2261', '0.4922', '0.728', '-0.673', '0.776', '0.291', '0.6006', '0.3193', '-0.353', '-0.462', '0.1097', '-0.1072', '-0.4836', '-0.2505', '0.944', '0.2185', '0.247', '-0.0432', '0.1996', '-0.4595', '-0.3782', '-0.3508', '-0.0406', '0.7583', '0.298', '-0.3975', '-0.3357', '0.2615', '-0.0175', '0.3303', '0.1587', '-0.849', '-0.5527', '0.1904', '0.07855', '0.3162', '-0.00461', '0.2087', '0.273', '0.473', '0.526', '-0.155', '-0.3235', '0.4966', '-0.1285', '-0.10736', '0.147', '-0.1625', '0.2261', '-0.822', '-0.4453', '0.4368', '-0.898', '-0.749', '-0.1381', '0.745', '0.09125', '0.02548', '-0.2825', '-0.0684', '0.05048', '-0.2703', '0.3674', '-0.5283', '-0.2764', '0.9507', '-0.3857', '-0.287', '0.2325', '-0.579', '0.4128', '-0.431', '0.12476', '0.4172']",C120191,,,,E34.51,,
mondo:0021024,"malaria, susceptibility to","['malaria, cerebral, reduced risk of', 'malaria, vivax, protection against', 'malaria, cerebral, resistance to', 'resistance to malaria due to G6PD deficiency', 'malaria, susceptibility to', 'malaria, cerebral, susceptibility to', 'malaria, Severe, susceptibility to', 'malaria, Severe, resistance to', 'malaria, protection against', 'malaria, resistance to']",,611162,,,"['-0.01223', '0.03656', '0.008095', '-0.02249', '0.01479', '-0.0766', '0.003187', '0.0313', '-0.01125', '-0.04227', '-0.01855', '-0.0003698', '-0.01064', '0.02953', '-0.02579', '-0.0419', '-0.011406', '-0.01319', '-0.04166', '-0.0816', '0.01501', '-0.03665', '0.06018', '0.00651', '-0.02103', '-0.02614', '-0.02489', '0.010506', '-0.01422', '-0.0532', '0.04657', '-0.009705', '0.0689', '-0.00792', '0.008934', '-0.01637', '-0.0442', '-0.0271', '-0.02336', '-0.06094', '0.01993', '-0.0408', '0.02435', '-0.0443', '-0.00565', '-0.058', '-0.0106', '0.03455', '-0.001653', '0.01602', '-0.01926', '-0.003448', '0.02853', '0.003145', '-0.01439', '0.01479', '0.04266', '-0.03247', '-0.0741', '0.000398', '0.0346', '0.0393', '-0.008484', '0.02298', '0.012726', '0.00878', '0.04843', '0.04913', '-0.08936', '0.0766', '-0.04233', '-0.00353', '0.00633', '-0.04276', '0.03418', '0.02783', '0.000734', '-0.01093', '-0.01306', '-0.005013', '-0.0259', '-0.01283', '-0.0201', '0.05295', '-0.0365', '-0.0041', '0.03723', '0.03156', '0.0699', '-0.01239', '0.0327', '0.05026', '-0.01', '0.00732', '0.10626', '0.0688', '0.04626', '-0.08704', '-0.03726', '0.001557']",,,,,,,
mondo:0021025,"cirrhosis, familial, with antigenemia","['cirrhosis, familial']",,118900,,,,,,,,,,
mondo:0021026,hereditary epidermal appendage anomaly,['genetic epidermal appendage anomaly'],,,183447,,,,,,,,,
mondo:0021029,hereditary sebaceous gland anomaly,['genetic sebaceous gland anomaly'],,,183460,,,,,,,,,
mondo:0021032,herpes zoster with dermatitis of eyelid,"['Herpes Zoster Dermatitis of Eyelid', 'Herpes zoster dermatitis of eyelids', 'Herpes zoster with dermatitis of eyelid', 'herpes zoster dermatitis of eyelid']",,,,C0019362,,C34696,,,053.20,,,
mondo:0021033,herpes zoster dermatitis,['herpes zoster dermatitis'],,,,,,C35619,,,,,,
mondo:0021034,hereditary alopecia,['genetic alopecia'],,,481771,,,,,,,,,
mondo:0021035,alopecia-intellectual disability syndrome 1,"['APMR', 'alopecia-mental retardation syndrome 1', 'APMR1', 'alopecia-intellectual disability syndrome 1']",0080628,203650,,C1859878,,,,,,,,
mondo:0021036,keratosis pilaris,['KP'],,,,,,C124070,,,,,,
mondo:0021038,Ewing sarcoma/peripheral primitive neuroectodermal tumor,"['Ewing family of tumors', 'tumours of the Ewing^s family', 'Ewing sarcoma/peripheral primitive neuroectodermal tumor', 'Ewing family of tumours', 'tumors of Ewing^s family', 'Ewing sarcoma family of tumours', 'Ewing^s sarcoma/peripheral primitive neuroectodermal tumor', 'Ewing^s family of tumours', 'tumors of the Ewing^s family', 'Ewing sarcoma/peripheral PNET', 'Ewing^s family of tumors', 'EFTs', 'tumours of Ewing^s family', 'Ewing sarcoma family of tumors', 'Ewing^s sarcoma/peripheral primitive neuroectodermal tumour']",,,,C3536893,,C27291,,,,,,
mondo:0021039,extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor,"['extraskeletal Ewing sarcoma/peripheral primitive neuroectodermal tumor', 'extraosseous Ewings sarcoma-primitive neuroepithelial tumor', 'extraosseous Ewing sarcoma/peripheral primitive neuroectodermal tumor', 'extraosseous Ewing^s tumor', 'extraosseous Ewing sarcoma/peripheral primitive neuroectodermal tumour', 'extraosseous Ewings sarcoma-primitive neuroepithelial tumour', 'extraosseous Ewing^s sarcoma/peripheral primitive neuroectodermal tumour', 'extraosseous Ewing^s sarcoma/peripheral primitive neuroectodermal tumor', 'extraosseous Ewing^s tumour']",4985,,,C1333514,,C27293,1000250,,,,,
mondo:0021040,pancreatic neoplasm,"['pancreas tumour', 'tumor of pancreas', 'tumour of pancreas', 'pancreatic neoplasm', 'neoplasm of the pancreas', 'pancreatic tumor', 'pancreas neoplasm', 'pancreatic tumour', 'pancreas neoplasm (disease)', 'tumor of the pancreas', 'tumour of the pancreas', 'pancreas', 'neoplasm of pancreas', 'pancreas tumor']",,,,,"['-0.10754', '0.1844', '0.04953', '-0.00214', '0.12054', '-0.1052', '0.1274', '0.09827', '-0.02196', '-0.05167', '-0.1098', '0.02936', '-0.012085', '0.005535', '-0.1908', '-0.09454', '-0.03827', '-0.09033', '-0.06903', '-0.2979', '0.002775', '-0.1697', '0.1636', '-0.1476', '-0.01799', '-0.1179', '0.01319', '-0.02304', '0.004856', '-0.137', '0.1627', '-0.03583', '0.1251', '-0.0679', '0.06537', '-0.04355', '-0.111', '-0.02495', '-0.05234', '-0.0422', '0.00361', '-0.1436', '0.09766', '-0.06134', '0.0142', '-0.09015', '-0.02463', '0.05698', '0.1271', '0.0984', '-0.003845', '0.01768', '0.0906', '0.143', '-0.094', '-0.01697', '0.0732', '-0.0759', '-0.2734', '-0.03436', '0.2527', '0.0623', '-0.05148', '0.02235', '-0.02325', '0.07434', '0.2451', '0.202', '-0.11285', '0.139', '-0.04626', '-0.04083', '0.1188', '-0.04617', '0.05856', '0.0364', '0.02362', '0.06384', '-0.01918', '-0.1863', '-0.262', '0.0471', '-0.09607', '0.01637', '-0.1355', '-0.08826', '0.1046', '0.0645', '0.1859', '-0.11755', '0.1815', '0.0993', '-0.014305', '-0.1125', '0.4292', '-0.03583', '0.1296', '-0.3057', '-0.084', '0.2015']",C3305,0003860,D010190,,,,
mondo:0021041,pleural solitary fibrous tumor,"['localized fibrous mesothelioma of pleura', 'solitary fibrous tumor of the pleura', 'pleural cavity solitary fibrous tumour', 'localised fibrous mesothelioma of the pleura', 'solitary fibrous tumour of the pleura', 'localized fibrous mesothelioma of the pleura', 'pleura solitary fibrous tumor', 'solitary fibrous tumour of pleura', 'fibroma of the pleura', 'pleural solitary fibrous tumor', 'pleural fibroma', 'pleural cavity solitary fibrous tumor', 'solitary fibrous tumor of pleura', 'pleura solitary fibrous tumour', 'fibroma of pleura', 'pleural Submesothelial fibroma', 'localised fibrous mesothelioma of pleura']",,,,C0334511,,C4457,1000835,,,,,
mondo:0021042,glioma,"['tumor of the neuroglia', 'tumour of the neuroglia', 'glial tumor', 'neoplasm of neuroglia', 'tumor of neuroglia', 'glial tumour', 'neuroglial tumour', 'neuroglial neoplasm', 'neuroglial tumor', 'neoplasm of the neuroglia', 'glial neoplasm', 'glioma', 'tumour of neuroglia']",,,182067,C0017638,,C3059,,D005910,,,,
mondo:0021043,mixed neoplasm,"['mixed tumour', 'mixed neoplasm', 'mixed tumor']",,,,,,C6930,,D018193,,,,
mondo:0021045,fibroepithelial neoplasm,"['fibroepithelial neoplasm', 'fibroepithelial tumor', 'fibroepithelial tumour']",,,,C0206649,,C3743,0007271,D018225,,,,
mondo:0021046,breast fibroepithelial neoplasm,"['BFN', 'breast fibroepithelial neoplasms', 'breast fibroepithelial neoplasm', 'breast fibroepithelial tumor', 'breast fibroepithelial tumour']",,,,C1511309,,C40405,,,,,,
mondo:0021047,breast phyllodes tumor,"['breast phyllodes tumor', 'phyllodes breast tumor', 'cystosarcoma phylloides - breast', 'phyllodes breast neoplasm', 'phyllodes neoplasm of breast', 'cystosarcoma phylloides of the breast', 'phyllodes neoplasm of the breast', 'phyllodes tumor of breast', 'phyllodes tumor of the breast', 'cystosarcoma phyllodes of breast', 'breast cystosarcoma phyllodes', 'breast phyllodes neoplasm', 'phyllodes tumour of the breast', 'cystosarcoma phyllodes of the breast', 'phyllodes breast tumour', 'phyllodes tumour of breast']",,,,,,C7575,,,,,,
mondo:0021048,benign mastocytoma,"['mastocytoma, benign', 'benign mastocytoma', 'MAST cell tumor, benign']",4658,,,C2242987,,C3217,,,,,,
mondo:0021049,vulvar neoplasm,"['vulvar tumour', 'vulvar tumor', 'vulval neoplasm', 'vulva tumor', 'neoplasm of mammalian vulva', 'vulva neoplasm', 'tumor of vulva', 'vulvar neoplasm', 'neoplasm of vulva', 'mammalian vulva tumor', 'neoplasm of the vulva', 'tumour of the vulva', 'tumour of mammalian vulva', 'tumor of the vulva', 'mammalian vulva neoplasm (disease)', 'mammalian vulva tumour', 'tumor of mammalian vulva', 'vulva tumour', 'tumour of vulva']",,,,,,C3443,,,239.5,,,
mondo:0021050,vaginal neoplasm,"['tumor of the vagina', 'neoplasm of vagina', 'vagina tumour', 'vagina tumor', 'tumor of vagina', 'vaginal tumour', 'vagina neoplasm', 'neoplasm of the vagina', 'vagina neoplasm (disease)', 'vaginal neoplasm', 'vaginal tumor', 'tumour of the vagina', 'tumour of vagina']",,,,,,C3437,1001447,,239.5,,,
mondo:0021052,parasympathetic paraganglioma,"['parasympathetic nervous system paraganglioma', 'parasympathetic paraganglioma', 'paraganglioma of parasympathetic nervous system', 'parasympathetic Extra-adrenal paraganglioma', 'parasympathetic Paraganglionic neoplasm']",,,,C0334416,,C4217,,,,,,
mondo:0021053,carotid body paraganglioma,"['paraganglioma of the carotid body', 'carotid body chemodectoma', 'tumour of carotid body', 'paraganglioma of carotid body', 'tumor of the carotid body', 'tumour of the carotid body', 'carotid body tumour', 'chemodectoma, undetermined', 'carotid body paraganglioma', 'chemodectoma', 'carotid body tumor', 'tumor of carotid body']",,,,C0007279,,C2932,,,,,,
mondo:0021054,bone sarcoma,"['sarcoma of bone', 'skeletal sarcoma', 'osseous sarcoma', 'bone sarcoma', 'sarcoma of the bone']",0080639,,223727,C1704327,,C9312,,,170.9,,10006007,
mondo:0021055,classic familial adenomatous polyposis,"['APC - adenomatous polyposis coli', 'colorectal adenomatous polyposis', 'familial adenomatous polyposis of the colon', 'familial adenomatous polyposis coli', 'familial multiple polyposis', 'familial adenomatous polyposis', 'FPC', 'familial polyposis', 'familial adenomatous polyposis syndrome', 'familial polyposis coli', 'adenomatous polyposis coli', 'hereditary adenomatous polyposis coli', 'hereditary polyposis coli', 'polyposis coli', 'classic FAP', 'FAP', 'adenomatous polyposis of the colon']",0050424,,733,CN240755,"['0.03906', '0.324', '-0.4192', '0.04034', '-0.0626', '-0.1133', '-0.02844', '0.751', '-0.4397', '-0.1685', '-0.2373', '0.1064', '-0.0942', '0.4114', '-0.6387', '-0.595', '0.1826', '-0.4937', '0.4436', '-0.3967', '-0.1694', '-0.2715', '0.1722', '-0.1617', '0.1964', '-0.1779', '0.1633', '-0.1388', '0.06714', '-0.7437', '0.7427', '-0.3137', '-0.757', '-0.0413', '0.01976', '0.2451', '-0.381', '-0.38', '0.1139', '0.1888', '0.1059', '-0.1714', '0.2764', '-0.303', '0.458', '0.1702', '-0.2856', '-0.1033', '0.2091', '0.04977', '-0.259', '0.01367', '-0.1475', '-0.2032', '-0.02121', '-0.4204', '-0.509', '0.4954', '-0.9277', '0.1465', '0.9478', '0.3599', '-0.1849', '-0.2212', '-0.11127', '0.575', '0.6636', '-0.2908', '-0.4622', '0.02164', '0.509', '-0.4055', '0.445', '-0.201', '0.59', '-0.2274', '0.1103', '-0.499', '0.2238', '-0.3923', '0.0874', '-0.1981', '0.3452', '-0.05414', '-1.015', '-0.158', '0.3513', '-0.4553', '0.2112', '-0.2744', '-0.1407', '-0.1843', '0.1781', '-0.02351', '0.7754', '-0.233', '0.515', '-0.5947', '-0.2264', '0.4075']",C3339,,,,,10056981,
mondo:0021056,familial adenomatous polyposis 1,"['polyposis, adenomatous intestinal', 'familial polyposis of the colon', 'brain tumor-polyposis syndrome 2', 'adenomatous polyposis coli, attenuated', 'familial adenomatous polyposis, attenuated', 'familial adenomatous polyposis 1', 'attenuated familial adenomatous polyposis caused by mutation in APC', 'adenomatous polyposis coli', 'FAP1', 'adenoma, periampullary, somatic', 'adenomatous polyposis of the colon', 'APC attenuated familial adenomatous polyposis', 'Gardner syndrome']",0080409,175100,99818,C0017097,"['0.10114', '0.5293', '-0.5327', '0.1902', '-0.0939', '-0.8276', '-0.1542', '0.6226', '-0.4033', '-0.2311', '0.158', '0.5386', '-0.3284', '0.008', '-0.01432', '-0.6626', '0.1055', '-0.232', '0.823', '-0.4744', '-0.009094', '-0.005585', '0.279', '0.005486', '0.7744', '0.1814', '0.0003126', '0.05374', '-0.1699', '-0.559', '0.561', '-0.673', '-0.1148', '-0.0467', '-0.1361', '-0.0927', '-0.3523', '0.1941', '-0.1272', '-0.1715', '0.1991', '-0.4038', '-0.4175', '0.05487', '0.3215', '-0.3484', '-0.4463', '0.0628', '0.491', '0.2466', '0.05542', '-0.05106', '-0.64', '-0.1917', '-0.2054', '-0.7866', '-0.0741', '0.505', '-0.6685', '-0.0746', '0.9136', '0.03174', '0.794', '0.02155', '-0.2146', '0.509', '0.5156', '0.1819', '-0.6504', '0.4028', '-0.08307', '0.2461', '0.781', '0.2812', '0.2766', '0.1351', '-0.2426', '0.5737', '-0.06088', '-0.151', '-0.3188', '0.336', '0.10065', '-0.4382', '-0.2869', '-0.537', '0.4148', '0.3647', '-0.08795', '0.00694', '0.03738', '-0.04553', '0.04285', '-0.264', '0.9097', '-0.2852', '0.4265', '-0.8164', '-0.3413', '-0.4485']",,,,,,,
mondo:0021057,classic or attenuated familial adenomatous polyposis,,,,,,,,,,,,,
mondo:0021058,neoplastic syndrome,"['tumour syndrome', 'cancer-related syndrome', 'neoplastic syndrome', 'tumor syndrome']",,,,,,C54705,,,,,,
mondo:0021060,RASopathy,"['Ras protein signal transduction disease', 'disorder of Ras protein signal transduction']",0080690,,536391,,,C179667,1001502,,,,,
mondo:0021061,neurofibromatosis,"['peripheral Neurofibromatosis', 'neurofibromatosis', 'Recklinghausen^s neurofibromatosis', 'neurofibromatosis syndrome', 'type IV neurofibromatosis of riccardi', 'von Reklinghausen disease', 'neurofibromatosis type 2', 'acoustic neurofibromatosis', 'central Neurofibromatosis', 'neurofibromatosis type IV', 'neurofibromatosis type 4']",8712,,,C0162678,,C6727,,D017253,237.72,,,
mondo:0021063,malignant colon neoplasm,"['malignant neoplasm of the colon', 'colon tumor, malignant', 'malignant colon tumor', 'cancer of colon', 'malignant colonic tumor', 'malignant tumour of colon', 'malignant colon neoplasm', 'malignant colon tumour', 'malignant colonic tumour', 'malignant neoplasm of colon', 'malignant tumor of colon', 'malignant tumor of the colon', 'colon cancer', 'malignant tumour of the colon', 'malignant colonic neoplasm', 'colon neoplasm, malignant']",219,,,C0007102,,C9242,,,153.9,,,
mondo:0021064,jugulotympanic paraganglioma,"['Glomus tumour', 'jugular body tumour', 'tumor of jugular body', 'neoplasm of glomus jugulare', 'jugular body tumor', 'tumour of glomus jugulare', 'Paraganglioma - glomus jugulare', 'glomus jugulare tumor', 'tumor of glomus jugulare', 'glomus jugulare neoplasm', 'neoplasm of jugular body', 'jugular body neoplasm (disease)', 'neoplasm of the glomus jugulare', 'tumor of the glomus jugulare', 'parasympathetic paraganglioma of basicranium', 'basicranium parasympathetic paraganglioma', 'jugular paraganglioma', 'glomus jugulare tumour', 'tumour of the glomus jugulare', 'tumour of jugular body', 'jugulotympanic paraganglioma', 'Glomus tumor']",,,,C0017671,,C3061,,,239.7,,,
mondo:0021065,pleural neoplasm,"['tumor of the pleura', 'pleural cavity tumour', 'tumor of pleura', 'neoplasm of pleura', 'pleural cavity tumor', 'neoplasm of the pleura', 'pleural cavity neoplasm (disease)', 'tumour of the pleura', 'pleura neoplasm (disease)', 'pleura tumor', 'neoplasm of pleural cavity', 'pleural neoplasm', 'pleural tumour', 'pleural tumor', 'pleura tumour', 'tumour of pleura']",,,,C0032229,,C3332,,D010997,,,,
mondo:0021066,urinary system neoplasm,"['urinary system tumor', 'urinary system tumour', 'tumour of urinary system', 'renal system neoplasm (disease)', 'neoplasm of the urinary system', 'tumor of renal system', 'tumor of the urinary tract', 'neoplasm of the urinary tract', 'tumor of urinary tract', 'tumor of the urinary system', 'tumor of urinary system', 'neoplasm of urinary tract', 'neoplasm of renal system', 'tumour of urinary tract', 'urinary tract neoplasm', 'urinary tract tumour', 'urinary tract tumor', 'neoplasm of urinary system', 'renal system tumour', 'renal system tumor', 'tumour of renal system', 'tumour of the urinary tract', 'tumour of the urinary system', 'urinary system neoplasm']",,,,,,C3431,,,239.5,,,
mondo:0021067,mediastinal germ cell tumor,"['germ cell tumour of mediastinum', 'germ cell tumour of the mediastinum', 'germ cell tumor of the mediastinum', 'germ cell neoplasm of mediastinum', 'germ cell neoplasm of the mediastinum', 'mediastinum germ cell tumour', 'thymic germ cell tumour', 'mediastinal germ cell tumor', 'thymic germ cell tumor', 'germ cell tumor of mediastinum', 'mediastinal germ cell neoplasm', 'mediastinum germ cell tumor']",,,,C1334655,,C6437,,,,,,
mondo:0021068,ovarian neoplasm,"['neoplasm of ovary', 'ovary neoplasm (disease)', 'ovary tumor', 'tumor of the ovary', 'tumour of the ovary', 'ovarian tumor', 'ovarian tumours', 'ovary tumour', 'ovarian tumour', 'ovarian neoplasm', 'tumour of ovary', 'tumor of ovary', 'ovarian tumors', 'neoplasm of the ovary']",,,,CN236629,,C4984,,,239.5,,,
mondo:0021069,malignant endocrine neoplasm,"['neoplasm of endocrine system', 'malignant endocrine tumour', 'Endocrine tumour', 'malignant tumor of endocrine gland', 'endocrine neoplasm, malignant', 'malignant neoplasm of endocrine gland', 'malignant endocrine gland neoplasm', 'malignant endocrine tumor', 'malignant tumour of the endocrine gland', 'malignant endocrine gland tumour', 'endocrine neoplasm', 'malignant tumor of the endocrine gland', 'Endocrine tumor', 'malignant endocrine neoplasm', 'endocrine gland cancer', 'endocrine cancer', 'malignant endocrine gland tumor', 'malignant tumour of endocrine gland', 'malignant neoplasm of the endocrine gland', 'cancer of endocrine gland']",170,,,,,C3575,,D004701,194.9,,,
mondo:0021070,sublingual gland carcinoma,"['carcinoma of the sublingual gland', 'sublingual gland cancer', 'carcinoma of sublingual gland', 'sublingual gland carcinoma']",,,,C0345611,,C8397,,,,,,
mondo:0021071,laryngeal neoplasm,"['tumour of the larynx', 'larynx neoplasm (disease)', 'neoplasm of larynx', 'tumour of larynx', 'larynx neoplasm', 'tumor of the larynx', 'laryngeal neoplasm', 'laryngeal tumour', 'laryngeal tumor', 'tumor of larynx', 'larynx tumor', 'neoplasm of the larynx', 'larynx tumour']",,,,C0023055,,C3156,0003817,D007822,,,,
mondo:0021072,sympathetic paraganglioma,"['chromaffin tumour', 'Chromaffinoma', 'chromaffin neoplasm', 'sympathetic nervous system paraganglioma', 'chromaffin tumor', 'sympathetic Paraganglionic neoplasm', 'paraganglioma of sympathetic nervous system', 'sympathetic paraganglioma']",,,,,,C4216,,C531777,,,,
mondo:0021073,paraneoplastic syndrome,['paraneoplastic syndrome'],,,,C0030472,,C3311,,D010257,,,,
mondo:0021074,precancerous condition,"['premalignant condition', 'precancerous state', 'precancerous condition', 'premalignant state']",,,,,,C3341,,D011230,,,,
mondo:0021075,neoplastic polyp,['neoplastic polyp'],,,,C1334941,,C7068,,,,,,
mondo:0021076,pancreatic exocrine neoplasm,"['tumour of the exocrine pancreas', 'exocrine pancreas neoplasm (disease)', 'neoplasm of exocrine pancreas', 'tumor of exocrine pancreas', 'tumour of exocrine pancreas', 'pancreatic exocrine tumor', 'tumor of the exocrine pancreas', 'exocrine pancreas tumour', 'exocrine pancreas tumor', 'pancreatic exocrine tumour', 'neoplasm of the exocrine pancreas', 'exocrine pancreas neoplasm', 'pancreatic exocrine neoplasm']",,,,C0345920,,C4445,,,235.5,,,
mondo:0021077,cystic neoplasm,"['cystic tumor', 'cystic neoplasm', 'cystic tumour']",,,,C1333190,,C6784,,,,,,
mondo:0021078,glandular papilloma,['glandular papilloma'],,,,C0205650,,C6880,,,,,,
mondo:0021079,childhood neoplasm,"['pediatric neoplasm', 'pediatric neoplasm (disease)', 'pediatric tumor', 'childhood tumour', 'paediatric tumour', 'paediatric neoplasm', 'childhood neoplasm', 'paediatric neoplasm (disease)', 'neoplasm (disease) of childhood', 'childhood tumor']",,,,,,C6283,,,,,,
mondo:0021080,blood vessel neoplasm,"['blood vessel neoplasm', 'neoplasm of blood vessel', 'blood vessel tumor', 'tumour of blood vessel', 'blood vessel tumour', 'tumor of blood vessel', 'blood vessel neoplasm (disease)']",,,,,,C7387,,,,,,
mondo:0021081,anti-NMDA receptor encephalitis,"['anti-NMDA receptor encephalitis', 'limbic encephalitis with N-methyl-D-aspartate receptor antibodies', 'limbic encephalitis with NMDA receptor antibodies']",,,217253,CN201135,,C94853,,D060426,,,,
mondo:0021082,Meckel diverticulum neoplasm,"['tumour of Meckel^s diverticulum', 'Meckel^s diverticulum tumour', 'Meckel^s diverticulum neoplasm (disease)', 'neoplasm of Meckel^s diverticulum', 'tumor of Meckel^s diverticulum', 'Meckel^s diverticulum tumor']",,,,C0345839,,,,,,,,
mondo:0021083,congenital fibrosis of extraocular muscles type 1,"['ophthalmoplegia, congenital', 'congenital fibrosis of extraocular muscles caused by mutation in KIF21A', 'fibrosis of extraocular muscles, congenital, 1', 'Feom1 locus', 'blepharoptosis with absent eye movements', 'fibrosis of extraocular muscles, congenital, 3B', 'KIF21A congenital fibrosis of extraocular muscles', 'CFEOM1']",0081015,135700,,,,,,,,,,
mondo:0021084,vision disorder,"['disorder of visual system', 'vision disorder', 'visual Field disorder', 'visual system disorder', 'visual disorder']",,,,C0042790,,C35126,,D014786,,,10047518,
mondo:0021085,gastric neoplasm,"['neoplasm of stomach', 'stomach neoplasm', 'gastric tumor', 'stomach neoplasm (disease)', 'stomach tumor', 'tumour of the stomach', 'tumour of stomach', 'tumor of the stomach', 'gastric neoplasm', 'gastric tumour', 'neoplasm of the stomach', 'tumor of stomach', 'stomach tumour']",,,,C0038356,,C3387,0003897,D013274,,,,
mondo:0021086,gingival neoplasm,"['gingiva tumour', 'gingival tumour', 'neoplasm of the gingiva', 'tumor of gingiva', 'gingiva neoplasm (disease)', 'gingival tumor', 'gum tumour', 'tumor of the gum', 'neoplasm of the gum', 'tumour of gingiva', 'tumour of gum', 'tumour of the gum', 'tumor of gum', 'neoplasm of gingiva', 'gum neoplasm', 'gingival neoplasm', 'gum tumor', 'tumour of the gingiva', 'neoplasm of gum', 'gingiva tumor', 'tumor of the gingiva']",,,,C0017570,,C3057,,,,,,
mondo:0021088,papillary meningioma,['papillary meningioma'],,,,C3163622,,C3904,,,,,,
mondo:0021089,peripheral nervous system cancer,"['malignant neoplasm of the peripheral nervous system', 'malignant neoplasm of the PNS', 'malignant tumour of the peripheral nervous system', 'malignant neoplasm of PNS', 'peripheral nervous system cancer', 'malignant peripheral nervous system neoplasm', 'malignant neoplasms, peripheral nerve', 'malignant tumor of PNS', 'cancer of peripheral nervous system', 'malignant PNS tumor', 'malignant PNS tumour', 'malignant neoplasm of peripheral nervous system', 'malignant tumour of peripheral nerve', 'malignant peripheral nerve tumour', 'malignant peripheral nerve tumor', 'malignant PNS neoplasm', 'malignant tumor of peripheral nerve', 'malignant tumour of PNS', 'malignant peripheral nervous system tumour', 'malignant tumour of the peripheral nerve', 'malignant tumor of the PNS', 'malignant tumour of the PNS', 'malignant tumour of peripheral nervous system', 'malignant tumor of the peripheral nerve', 'malignant neoplasm of peripheral nerve', 'peripheral nervous system neoplasms, malignant', 'malignant neoplasm of the peripheral nerve', 'malignant peripheral nervous system tumor', 'malignant peripheral nerve neoplasm', 'malignant tumor of the peripheral nervous system', 'malignant tumor of peripheral nervous system']",,,,C0751428,,C4961,,,171.9,,,
mondo:0021090,lipid-rich breast carcinoma,"['breast lipid-rich carcinoma', 'lipid secreting breast carcinoma', 'lipid-rich breast carcinoma']",7076,,,C1517894,,C40365,,,,,,
mondo:0021091,papillary cystadenoma,"['papillary cystadenoma', 'cystadenoma, papillary, benign']",,,,C0010636,,C2974,,D018292,,,,
mondo:0021092,fallopian tube neoplasm,"['fallopian tube tumour', 'tumour of the fallopian tube', 'fallopian tube tumor', 'tumor of fallopian tube', 'neoplasm of fallopian tube', 'tumor of the fallopian tube', 'tumour of fallopian tube', 'fallopian tube neoplasm (disease)', 'fallopian tube neoplasm', 'neoplasm of the fallopian tube']",,,,C0015558,,C3032,,D005185,239.5,,,
mondo:0021093,cranioectodermal dysplasia 1,"['IFT122 cranioectodermal dysplasia', 'cranioectodermal dysplasia 1', 'Sensenbrenner syndrome', 'CED1', 'cranioectodermal dysplasia caused by mutation in IFT122', 'cranioectodermal dysplasia type 1', 'Levin syndrome 1']",0080803,218330,,,,,,,,,,
mondo:0021094,immunodeficiency disease,"['immunodeficiency syndrome', 'immunodeficiency', 'immunodeficiency disorder', 'immuno-deficiency']",,,,C0021051,"['-0.02031', '0.04648', '0.006763', '-0.01924', '0.001637', '-0.05472', '0.014854', '0.02943', '-0.04645', '-0.00923', '-0.0161', '-0.003546', '-0.01569', '0.01228', '0.00535', '-0.03995', '0.00569', '-0.03065', '-0.02745', '-0.08325', '-0.01078', '-0.01572', '0.05948', '-0.02368', '0.01608', '-0.02782', '-0.005413', '0.000958', '0.004444', '-0.0481', '0.0365', '0.02328', '0.07043', '0.011475', '0.01762', '-0.00839', '-0.03763', '-0.02922', '-0.01442', '-0.04486', '-0.00307', '-0.03787', '0.01275', '-0.03111', '-0.00478', '-0.03592', '-0.02576', '0.02362', '0.02667', '0.01502', '-0.01616', '-0.01165', '0.04376', '0.009514', '-0.03796', '-0.02672', '0.0271', '-0.0314', '-0.06158', '0.006752', '0.04074', '0.0207', '-0.00429', '0.003283', '0.02055', '0.00752', '0.04572', '0.03735', '-0.04538', '0.0647', '-0.05035', '0.01008', '0.00503', '-0.02962', '0.02042', '0.01743', '0.02095', '-0.00863', '-0.00484', '-0.01942', '-0.006626', '-0.02094', '-0.02019', '0.04138', '-0.0002316', '-0.002491', '0.04684', '0.05386', '0.069', '0.005962', '0.03348', '0.03918', '-0.000774', '0.02727', '0.122', '0.0499', '0.0337', '-0.0756', '-0.00728', '0.032']",C3131,,,279.3,,,
mondo:0021095,parkinsonian disorder,,0080855,,,,,,,D020734,,,,
mondo:0021096,papillary epithelial neoplasm,['papillary epithelial neoplasm'],,,,C1335324,,C8429,,,,,,
mondo:0021097,intraductal breast papilloma,"['intraductal papilloma of breast', 'ductal breast papilloma', 'intraductal papilloma of the breast', 'mammary duct papilloma', 'duct papilloma of breast', 'duct papilloma of the breast', 'breast papilloma', 'papilloma of the breast', 'papilloma of breast', 'breast duct papilloma', 'intraductal breast papilloma']",1626,,,,,C3863,1000306,,,,,
mondo:0021098,papillomatosis,['papillomatosis'],,,,,,C3713,,,,,,
mondo:0021099,intraductal papillomatosis,"['intraductal papillomatosis', 'duct papillomatosis']",,,,C0334377,,C7363,,,,,,
mondo:0021100,breast neoplasm,"['breast tumour', 'tumour of the breast', 'breast tumor', 'neoplasm of breast', 'breast neoplasm (disease)', 'tumour of breast', 'neoplasm of the breast', 'breast neoplasm', 'tumor of the breast', 'tumor of breast', 'neoplasm, breast']",,,,CN236627,"['-0.09735', '0.1722', '-0.009254', '-0.05356', '0.2788', '-0.1365', '0.2394', '0.02711', '-0.02531', '0.004234', '0.079', '0.1489', '-0.1815', '0.1406', '-0.2356', '-0.2285', '-0.01967', '-0.12354', '-0.1176', '-0.2423', '-0.1766', '-0.2737', '0.3953', '-0.3809', '0.133', '-0.2314', '-0.0001988', '-0.1354', '0.04974', '-0.2551', '0.4336', '-0.1896', '0.1449', '-0.1879', '0.04874', '-0.0667', '-0.2852', '0.0589', '-0.02528', '-0.03522', '0.07935', '-0.01227', '-0.1345', '-0.03162', '0.224', '-0.00656', '-0.08936', '0.1082', '0.1896', '0.0709', '0.1975', '0.005276', '0.02937', '0.2228', '-0.3167', '0.1367', '0.1792', '-0.1328', '-0.2944', '0.048', '0.3132', '0.2174', '0.01107', '0.1726', '-0.0635', '0.0786', '0.293', '0.3086', '-0.2377', '0.1597', '0.02354', '0.06003', '0.1405', '-0.1002', '0.05035', '0.00912', '0.03897', '0.153', '-0.0847', '-0.4165', '-0.3132', '-0.0783', '0.1214', '0.001924', '-0.2008', '-0.1125', '0.1555', '-0.1225', '0.1984', '-0.08954', '0.1004', '0.384', '-0.1009', '-0.1401', '0.577', '-0.04242', '0.2085', '-0.2094', '-0.2192', '0.1628']",C2910,0003869,D001943,239.3,,,
mondo:0021101,appendix L-cell glucagon-like peptide-producing neuroendocrine tumor,"['appendix L-cell NET', 'L-cell glucagon-like peptide-producing neuroendocrine tumour of vermiform appendix', 'appendiceal L-cell glucagon-like peptide-producing neuroendocrine tumor', 'appendiceal L-cell glucagon-like peptide-producing NET', 'appendiceal L-cell glucagon-like peptide producing tumor', 'appendix L-cell glucagon-like peptide-producing neuroendocrine tumor', 'vermiform appendix L-cell glucagon-like peptide-producing neuroendocrine tumor', 'L-cell glucagon-like peptide-producing neuroendocrine tumor of vermiform appendix', 'vermiform appendix L-cell glucagon-like peptide-producing neuroendocrine tumour', 'appendiceal L-cell glucagon-like peptide-producing neuroendocrine tumour', 'appendix L-cell glucagon-like peptide-producing NET', 'malignant appendiceal L-cell glucagon-like peptide producing tumour', 'appendiceal L-cell glucagon-like peptide producing tumour', 'malignant appendiceal L-cell glucagon-like peptide producing tumor', 'malignant appendiceal glucagonoma']",8151,,,C3274138,,C27445,,,,,,
mondo:0021102,prostate phyllodes tumor,"['phyllodes neoplasm of the prostate', 'phyllodes tumour of prostate', 'prostate gland phyllodes tumour', 'cystosarcoma phyllodes of the prostate', 'prostate phyllodes neoplasm', 'phyllodes tumor of the prostate', 'cystosarcoma phyllodes of prostate', 'phyllodes tumour of the prostate', 'malignant phyllodes tumour of prostate (subtype)', 'phyllodes tumor of prostate', 'prostate gland phyllodes tumor', 'prostate phyllodes tumor', 'malignant phyllodes tumor of prostate (subtype)', 'phyllodes neoplasm of prostate', 'prostate cystosarcoma phyllodes']",,,498228,C1335409,,C7574,,,,,,
mondo:0021104,alcoholic fatty liver disease,"['alcoholic fatty liver', 'alcoholic Steatohepatitis']",,,,C2718067,,,,D005235,571.0,,,
mondo:0021105,NAFLD1,"['fatty liver disease, nonalcoholic, susceptibility to, 1', 'NAFLD1', 'liver disease, alcoholic, susceptibility to, 1']",,613282,,,,,,,,,,
mondo:0021106,laminopathy,,,,98301,CN236383,,,,D000083083,,,,
mondo:0021107,narcolepsy,"['narcolepsy, without cataplexy', 'narcolepsy', 'paroxysmal sleep']",8986,,619284,C0027404,,C84489,,D009290,347.00,,,
mondo:0021108,meningitis,"['meningitis', 'meningitis (disease)', 'meninx inflammation']",,,,,,C26828,,D008581,322.9,,,
mondo:0021109,inverted urothelial papilloma,"['IUP', 'urinary tract inverted papilloma', 'inverted papilloma of urinary tract', 'inverted urothelial papilloma', 'urothelium inverted papilloma']",,,,C1334282,,C6192,,,,,,
mondo:0021110,sweat gland adenoma,"['adenoma, sweat gland, benign', 'sweat gland adenoma', 'adenoma of sweat gland', 'adenoma of the sweat gland']",,,,,,C7560,,,,,,
mondo:0021111,ureter neoplasm,"['neoplasms of ureter', 'tumor of ureter', 'tumor of the ureter', 'neoplasm of the ureter', 'ureter neoplasm (disease)', 'ureter tumour', 'ureteral neoplasm', 'neoplasm of ureter', 'ureteral tumour', 'ureter tumor', 'ureteral tumor', 'tumour of ureter', 'tumour of the ureter', 'ureter neoplasm', 'neoplasms of the ureter']",,,,,,C3427,0003844,,239.5,,,
mondo:0021112,scrotum cancer,"['malignant tumour of scrotum', 'malignant tumour of the scrotum', 'scrotum cancer', 'cancer of scrotum', 'malignant tumor of scrotum', 'malignant scrotal tumor', 'malignant neoplasm of the scrotum', 'malignant scrotal tumour', 'malignant scrotum neoplasm', 'malignant tumor of the scrotum', 'malignant neoplasm of scrotum', 'malignant scrotal neoplasm']",,,,C0153604,,C3560,,,187.7,,,
mondo:0021113,respiratory failure,"['acute and chronic respiratory failure', 'failure, respiratory', 'chronic respiratory failure', 'acute-on-chronic respiratory failure', 'respiratory insufficiency/failure', 'acute respiratory failure', 'respiratory failure']",11162,,,C1145670,,C26872,,D012131,518.83,,,
mondo:0021114,Bartholin gland neoplasm,"['major vestibular gland tumor', 'Bartholin gland neoplasm', 'tumour of the Bartholin^s gland', 'tumor of the Bartholin^s gland', 'tumour of Bartholin^s gland', 'neoplasm of Bartholin^s gland', 'tumour of major vestibular gland', 'tumor of Bartholin^s gland', 'major vestibular gland neoplasm (disease)', 'Bartholin^s gland tumor', 'neoplasm of major vestibular gland', 'Bartholin^s gland neoplasm', 'Bartholin^s gland tumour', 'tumor of major vestibular gland', 'neoplasm of the Bartholin^s gland', 'major vestibular gland tumour']",,,,,,C6434,,,,,,
mondo:0021445,benign neoplasm of oral cavity,"['benign mouth neoplasm', 'benign tumour of the oral cavity', 'benign mouth tumor', 'benign oral cavity tumor', 'oral cavity benign neoplasm', 'benign oral cavity tumour', 'benign tumour of the mouth', 'benign tumor of the oral cavity', 'benign tumour of mouth', 'benign mouth tumour', 'benign tumour of oral cavity', 'benign tumor of oral cavity', 'benign tumor of mouth', 'benign neoplasm of the oral cavity', 'benign oral cavity neoplasm', 'benign neoplasm of mouth', 'benign neoplasm of the mouth', 'benign tumor of the mouth']",,,,C0347197,,C7607,,,210.4,,,
mondo:0021446,benign neoplasm of epiglottis,"['benign epiglottic tumor', 'benign Epiglottis tumor', 'benign epiglottic neoplasm', 'benign tumor of Epiglottis', 'benign neoplasm of the Epiglottis', 'benign epiglottic tumour', 'benign tumour of the Epiglottis', 'benign tumour of Epiglottis', 'benign Epiglottis tumour', 'benign tumor of the Epiglottis', 'epiglottis benign neoplasm', 'benign Epiglottis neoplasm']",,,,C0347236,,C4606,,,,,,
mondo:0021447,benign neoplasm of testis,"['benign tumor of the testis', 'benign neoplasm of the testis', 'benign tumour of testis', 'benign tumor of testis', 'benign testicular neoplasm', 'benign testicular tumor', 'benign testicular tumour', 'testis benign neoplasm', 'benign tumour of the testis']",,,,C0154007,,C3612,,,222.0,,,
mondo:0021449,benign neoplasm of stomach,"['benign gastric tumour', 'benign stomach neoplasms', 'benign tumour of stomach', 'benign gastric tumors', 'benign gastric neoplasm', 'benign tumours of the stomach', 'benign gastric tumor', 'benign tumors of stomach', 'gastric neoplasms, benign', 'benign tumour of the stomach', 'benign tumors of the stomach', 'benign gastric tumours', 'benign stomach tumors', 'stomach neoplasms, benign', 'stomach tumors, benign', 'benign tumours of stomach', 'benign neoplasm of the stomach', 'benign tumor of stomach', 'stomach benign neoplasm', 'benign stomach tumours', 'benign tumor of the stomach', 'gastric tumors, benign']",,,,C0153943,,C3599,,,211.1,D13.1,,
mondo:0021450,benign neoplasm of heart,"['benign Cardiac tumour', 'benign tumour of the heart', 'heart benign neoplasm', 'benign Cardiac neoplasm', 'benign neoplasm of the heart', 'benign tumor of the heart', 'benign tumour of heart', 'benign heart tumor', 'benign tumor of heart', 'benign heart neoplasm', 'benign heart tumour', 'benign Cardiac tumor']",,,,C0153957,,C3605,,,212.7,D15.1,,
mondo:0021451,benign neoplasm of brain,"['benign tumour of brain', 'benign tumour of the brain', 'brain neoplasms, benign', 'benign brain tumour', 'benign tumor of the brain', 'brain benign neoplasm', 'benign neoplasm of the brain', 'benign brain tumor', 'benign brain neoplasm', 'benign tumor of brain']",,,,,,C4781,1000107,,225.0,,,
mondo:0021452,benign neoplasm of cornea,"['benign cornea neoplasm', 'benign corneal tumour', 'benign corneal neoplasm', 'benign cornea tumour', 'benign neoplasm of the cornea', 'benign tumor of cornea', 'benign cornea tumor', 'benign tumour of cornea', 'benign tumor of the cornea', 'benign tumour of the cornea', 'cornea benign neoplasm', 'benign corneal tumor']",,,,C0154026,,C3623,,,224.4,,,
mondo:0021453,benign neoplasm of retina,"['benign retinal tumour', 'benign tumor of the retina', 'benign retina tumor', 'benign retinal neoplasm', 'benign retina tumour', 'benign neoplasm of the retina', 'benign retina neoplasm', 'benign tumor of retina', 'benign tumour of retina', 'retina benign neoplasm', 'benign retinal tumor', 'benign tumour of the retina']",,,,C0154027,,C3624,,,224.5,,,
mondo:0021454,benign neoplasm of eye,"['benign tumor of eye', 'eye benign neoplasm', 'benign tumor of the eye', 'benign tumour of eye', 'benign neoplasm of the eye', 'benign eye tumor', 'benign eye tumour', 'benign ocular neoplasm', 'benign ocular tumor', 'benign tumour of the eye', 'benign eye neoplasm', 'benign ocular tumour']",,,,C0496897,,C4780,,,224.9,,,
mondo:0021455,benign neoplasm of neck,"['neck benign neoplasm', 'benign tumour of neck', 'benign tumor of the neck', 'benign neoplasm of the neck', 'benign neck tumor', 'benign neck neoplasm', 'benign neck tumour', 'benign tumour of the neck', 'benign tumor of neck']",,,,C0684815,,C4884,,,229.8,,,
mondo:0021456,benign neoplasm of sternum,"['benign sternal tumour', 'sternum benign neoplasm', 'benign neoplasm of the sternum', 'benign sternal tumor', 'benign tumor of the sternum', 'benign sternal neoplasm', 'benign tumour of the sternum', 'benign tumor of sternum', 'benign tumour of sternum']",,,,C0347312,,C8416,,,,,,
mondo:0021457,benign neoplasm of pleura,"['benign tumor of pleura', 'pleura benign neoplasm', 'benign tumour of pleura', 'benign pleural neoplasm', 'benign pleural tumour', 'benign tumor of the pleura', 'benign pleural tumor', 'benign neoplasm of the pleura', 'benign tumour of the pleura']",,,,C0153955,,C3603,,,212.4,,,
mondo:0021458,benign neoplasm of penis,"['benign penile tumour', 'benign tumor of penis', 'benign tumor of the penis', 'penis benign neoplasm', 'benign tumour of penis', 'benign penile neoplasm', 'benign penile tumor', 'benign tumour of the penis', 'benign neoplasm of the penis']",,,,C0149627,,C3489,,,222.1,D29.0,,
mondo:0021459,benign neoplasm of esophagus,"['benign neoplasm of the oesophagus', 'benign esophageal neoplasm', 'benign oesophagus neoplasm', 'benign tumour of the oesophagus', 'benign tumor of the esophagus', 'benign neoplasm of the esophagus', 'esophagus benign neoplasm', 'benign esophagus tumor', 'benign esophageal tumor', 'benign tumor of esophagus', 'benign tumour of oesophagus', 'benign oesophagus tumour', 'oesophagus benign neoplasm', 'benign esophagus neoplasm', 'benign esophageal tumour']",,,,C0153942,,C3598,,,211.0,D13.0,,
mondo:0021460,benign neoplasm of salivary gland,"['benign neoplasm of the salivary gland', 'benign salivary gland neoplasm', 'benign salivary gland tumor', 'benign salivary gland tumour', 'benign tumor of the salivary gland', 'benign tumour of salivary gland', 'salivary gland neoplasm, benign', 'benign tumour of the salivary gland', 'saliva-secreting gland benign neoplasm', 'benign tumor of salivary gland']",,,,C0347206,,C4600,,,,,,
mondo:0021461,benign neoplasm of hypopharynx,"['benign tumour of hypopharynx', 'hypopharynx benign neoplasm', 'benign hypopharyngeal tumour', 'benign tumor of hypopharynx', 'hypopharyngeal neoplasm, benign', 'benign hypopharyngeal tumor', 'benign hypopharyngeal neoplasm', 'benign tumour of the hypopharynx', 'benign neoplasm of the hypopharynx', 'benign tumor of the hypopharynx']",,,,C0153939,,C3596,,,210.8,D10.7,,
mondo:0021462,benign neoplasm of rectum,"['rectal tumors, benign', 'benign tumour of rectum', 'benign tumour of the rectum', 'rectum benign neoplasm', 'benign tumor of rectum', 'benign rectal neoplasm', 'benign neoplasm of the rectum', 'benign rectal neoplasms', 'benign rectal tumour', 'benign rectal tumours', 'benign tumor of the rectum', 'rectal neoplasms, benign', 'benign rectal tumor', 'benign rectal tumors']",,,,C0496867,,C4774,,,,D12.8,,
mondo:0021463,benign neoplasm of parathyroid gland,"['benign tumor of the parathyroid gland', 'benign parathyroid gland tumor', 'benign parathyroid neoplasm', 'benign tumor of the parathyroid', 'benign parathyroid tumour', 'benign parathyroid tumor', 'parathyroid tumour benign', 'parathyroid tumor benign', 'parathyroid gland benign neoplasm', 'benign neoplasm of parathyroid', 'benign neoplasm of the parathyroid gland', 'benign tumour of the parathyroid', 'benign parathyroid gland neoplasm', 'benign tumor of parathyroid gland', 'benign tumor of parathyroid', 'benign tumour of parathyroid gland', 'benign parathyroid gland tumour', 'benign tumour of the parathyroid gland', 'benign neoplasm of the parathyroid', 'benign tumour of parathyroid']",60008,,,C0154041,,C3630,,,227.1,D35.1,,
mondo:0021464,benign neoplasm of cecum,"['benign cecum tumor', 'benign neoplasm of the cecum', 'benign tumour of the cecum', 'benign tumor of cecum', 'benign tumor of the cecum', 'benign tumour of cecum', 'caecum benign neoplasm', 'benign cecum tumour', 'benign cecum neoplasm']",,,,C0496859,,C4772,,,,D12.0,,
mondo:0021465,benign neoplasm of appendix,"['vermiform appendix benign neoplasm', 'benign appendix tumor', 'benign appendix neoplasm', 'benign tumour of appendix', 'benign appendix tumour', 'benign tumor of appendix', 'benign tumour of the appendix', 'benign neoplasm of the appendix', 'benign tumor of the appendix']",,,,C0496860,,C4773,,,,D12.1,,
mondo:0021467,benign neoplasm of renal pelvis,"['benign renal pelvis tumour', 'benign tumor of renal pelvis', 'benign tumour of the renal pelvis', 'benign renal pelvis neoplasm', 'benign tumor of the renal pelvis', 'benign tumour of renal pelvis', 'benign neoplasm of the renal pelvis', 'benign renal pelvis tumor', 'renal pelvis benign neoplasm', 'benign kidney pelvis neoplasm']",,,,C0154015,,C3616,1000118,,223.1,,,
mondo:0021468,benign neoplasm of adrenal medulla,"['benign tumor of adrenal medulla', 'benign tumour of the adrenal medulla', 'benign adrenal medulla neoplasm', 'benign tumor of the adrenal medulla', 'benign neoplasm of the adrenal medulla', 'benign tumour of adrenal medulla', 'benign adrenal medulla tumor', 'adrenal medulla benign neoplasm', 'benign adrenal medulla tumour']",,,,C0686512,,C4895,,,,,,
mondo:0021469,benign neoplasm of anus,"['benign anal neoplasm', 'benign tumor of anus', 'anus benign neoplasm', 'benign tumor of the anus', 'benign tumour of anus', 'benign anal tumour', 'benign neoplasm of the anus', 'benign anal tumor', 'benign tumour of the anus']",,,,C0347276,,C4611,,,,,,
mondo:0021470,benign neoplasm of pancreas,"['benign neoplasm of the pancreas', 'benign pancreatic tumor', 'pancreatic neoplasm, benign', 'pancreas benign neoplasm', 'benign tumor of pancreas', 'benign tumour of pancreas', 'benign pancreas tumor', 'benign pancreas neoplasm', 'benign tumour of the pancreas', 'pancreas tumor, benign', 'pancreas neoplasm, benign', 'benign pancreatic neoplasm', 'pancreatic tumor, benign', 'benign pancreatic tumour', 'benign tumor of the pancreas', 'benign pancreas tumour']",,,,C0347284,,C4612,,,,D13.6,,
mondo:0021471,benign neoplasm of endometrium,"['benign tumor of the endometrium', 'benign endometrial neoplasm', 'endometrium benign neoplasm', 'benign endometrium neoplasm', 'benign endometrial tumour', 'benign endometrium tumor', 'benign endometrium tumour', 'benign neoplasm of the endometrium', 'benign tumor of endometrium', 'benign tumour of the endometrium', 'benign endometrial tumor', 'benign tumour of endometrium']",,,,C0686239,,C4894,,,,,,
mondo:0021472,benign neoplasm of scrotum,"['benign scrotal tumour', 'benign tumour of scrotum', 'benign tumor of the scrotum', 'benign scrotal neoplasm', 'benign neoplasm of the scrotum', 'benign tumor of scrotum', 'benign tumour of the scrotum', 'benign scrotal tumor', 'scrotum benign neoplasm']",,,,C0154011,,C3615,,,222.4,D29.4,,
mondo:0021473,benign neoplasm of epididymis,"['benign tumour of the epididymis', 'epididymis benign neoplasm', 'benign epididymal tumour', 'benign tumor of epididymis', 'benign tumour of epididymis', 'benign neoplasm of the epididymis', 'benign epididymal neoplasm', 'benign epididymal tumor', 'benign tumor of the epididymis']",,,,C0154010,,C3614,,,222.3,,,
mondo:0021474,benign neoplasm of ear,"['benign Ear neoplasm', 'benign Ear tumor', 'aural neoplasms, benign', 'benign tumour of the Ear', 'benign tumour of Ear', 'benign tumor of the Ear', 'benign Ear tumour', 'ear benign neoplasm', 'benign tumor of Ear', 'benign neoplasm of the Ear']",,,,C0347354,,C8417,,,,,,
mondo:0021475,benign neoplasm of nasal cavity,"['nasal cavity benign neoplasm', 'benign tumor of nasal cavity', 'benign tumor of the nasal cavity', 'benign neoplasm of the nasal cavity', 'benign nasal cavity neoplasm', 'benign nasal cavity tumour', 'benign tumour of the nasal cavity', 'benign tumour of nasal cavity', 'benign nasal cavity tumor']",,,,C0347215,,C4603,,,212.0,,,
mondo:0021476,benign neoplasm of tongue,"['benign tongue neoplasm', 'benign tongue tumour', 'benign neoplasm of the tongue', 'benign tumor of the tongue', 'benign tumour of tongue', 'benign tumour of the tongue', 'tongue benign neoplasm', 'tongue neoplasm, benign', 'benign tongue tumor', 'benign tumor of tongue']",,,,C0153933,,C3592,,,210.1,D10.1,,
mondo:0021477,benign neoplasm of sphenoidal sinus,"['benign tumor of the sphenoid sinus', 'benign sphenoidal sinus tumor', 'sphenoidal sinus benign neoplasm', 'benign neoplasm of the sphenoid sinus', 'benign neoplasm of the sphenoidal sinus', 'benign sphenoid sinus tumour', 'benign tumor of sphenoidal sinus', 'benign sphenoidal sinus neoplasm', 'benign sphenoid sinus tumor', 'benign sphenoid sinus neoplasm', 'benign tumor of sphenoid sinus', 'benign tumor of the sphenoidal sinus', 'benign tumour of the sphenoidal sinus', 'benign tumour of sphenoidal sinus', 'benign neoplasm of sphenoid sinus', 'benign sphenoidal sinus tumour', 'benign tumour of sphenoid sinus', 'benign tumour of the sphenoid sinus']",,,,C0345678,,C4422,,,212.0,,,
mondo:0021478,benign neoplasm of nasopharynx,"['benign tumor of the nasopharynx', 'benign neoplasm of the nasopharynx', 'benign tumour of the nasopharynx', 'nasopharyngeal neoplasm, benign', 'benign nasopharyngeal tumour', 'benign tumor of nasopharynx', 'benign tumour of nasopharynx', 'benign nasopharyngeal neoplasm', 'benign nasopharyngeal tumor', 'nasopharynx benign neoplasm']",,,,C0153938,,C3595,,,210.7,D10.6,,
mondo:0021479,benign neoplasm of oropharynx,"['oropharyngeal neoplasm benign', 'benign tumor of the oropharynx', 'benign oropharyngeal tumour', 'benign tumour of the oropharynx', 'oropharynx benign neoplasm', 'benign oropharyngeal neoplasm', 'benign tumour of oropharynx', 'benign neoplasm of the oropharynx', 'benign oropharyngeal tumor', 'benign tumor of oropharynx']",,,,C0347229,,C4604,,,210.6,,,
mondo:0021480,benign neoplasm of soft palate,"['benign tumor of soft palate', 'benign tumour of soft palate', 'benign neoplasm of the soft palate', 'benign tumour of the soft palate', 'benign tumor of the soft palate', 'soft palate benign neoplasm', 'benign soft palate tumor', 'benign soft palate neoplasm', 'benign soft palate tumour']",,,,C0345557,,C4404,,,210.4,,,
mondo:0021481,benign neoplasm of submandibular gland,"['benign submandibular gland tumour', 'benign tumour of the submandibular gland', 'benign submandibular gland neoplasm', 'benign submandibular gland tumor', 'benign tumor of submandibular gland', 'benign tumour of submandibular gland', 'submandibular gland benign neoplasm', 'benign neoplasm of the submandibular gland', 'benign tumor of the submandibular gland']",,,,C0685988,,C4891,,,,,,
mondo:0021482,benign neoplasm of middle ear,"['benign middle Ear neoplasm', 'benign tumour of the middle Ear', 'benign middle Ear tumour', 'benign tumor of middle Ear', 'benign tumour of middle Ear', 'middle ear benign neoplasm', 'benign middle Ear tumor', 'benign tumor of the middle Ear', 'benign neoplasm of the middle Ear']",,,,C0347213,,C4602,,,212.0,,,
mondo:0021483,benign neoplasm of frontal sinus,"['benign frontal sinus tumor', 'benign tumour of the frontal sinus', 'benign neoplasm of the frontal sinus', 'benign tumor of the frontal sinus', 'frontal sinus benign neoplasm', 'benign tumour of frontal sinus', 'benign frontal sinus neoplasm', 'benign tumor of frontal sinus', 'benign frontal sinus tumour']",,,,C0345674,,C4420,,,212.0,,,
mondo:0021484,benign neoplasm of maxillary sinus,"['benign neoplasm of the maxillary antrum', 'benign maxillary antrum neoplasm', 'benign tumour of maxillofacial sinus', 'benign tumour of maxillary sinus', 'benign tumor of the maxillary sinus', 'benign maxillary sinus tumour', 'benign maxillofacial sinus neoplasm', 'benign maxillary antrum tumor', 'benign neoplasm of maxillary antrum', 'benign tumor of maxillary sinus', 'benign maxillofacial sinus tumor', 'benign neoplasm of the maxillary sinus', 'benign neoplasm of maxillofacial sinus', 'maxillary sinus benign neoplasm', 'benign tumour of the maxillary sinus', 'benign tumor of the maxillofacial sinus', 'benign maxillary antrum tumour', 'benign maxillofacial sinus tumour', 'benign tumor of maxillofacial sinus', 'benign maxillary sinus neoplasm', 'benign tumour of maxillary antrum', 'benign tumour of the maxillary antrum', 'benign maxillary sinus tumor', 'benign tumor of the maxillary antrum', 'benign tumour of the maxillofacial sinus', 'benign neoplasm of the maxillofacial sinus', 'benign tumor of maxillary antrum']",,,,C0345666,,C4414,,,212.0,,,
mondo:0021485,benign neoplasm of iris,"['benign iris neoplasm', 'benign iris tumour', 'benign tumor of iris', 'benign iris tumor', 'benign tumor of the iris', 'benign tumour of the iris', 'benign neoplasm of the iris', 'iris benign neoplasm', 'benign tumour of iris']",,,,C0346374,,C4555,,,224.0,,,
mondo:0021486,benign neoplasm of ciliary body,"['benign neoplasm of the ciliary body', 'benign ciliary body tumour', 'ciliary body benign neoplasm', 'benign ciliary body neoplasm', 'benign tumor of ciliary body', 'benign tumour of ciliary body', 'benign ciliary body tumor', 'benign tumour of the ciliary body', 'benign tumor of the ciliary body']",,,,C0496894,,C4779,,,224.0,,,
mondo:0021487,benign neoplasm of choroid,"['benign tumor of the choroid', 'benign tumour of the choroid', 'benign choroid tumour', 'optic choroid benign neoplasm', 'benign tumour of choroid', 'benign neoplasm of the choroid', 'benign tumor of choroid', 'benign choroid tumor', 'benign choroid neoplasm']",,,,C0154028,,C3625,,,224.6,,,
mondo:0021488,benign neoplasm of lacrimal gland,"['benign lacrimal gland tumor', 'benign neoplasm of the lacrimal gland', 'benign lacrimal gland neoplasm', 'lacrimal gland benign neoplasm', 'benign tumour of the lacrimal gland', 'benign lacrimal gland tumour', 'benign tumor of the lacrimal gland', 'benign tumor of lacrimal gland', 'benign tumour of lacrimal gland']",,,,C0154024,,C3621,,,224.2,,,
mondo:0021489,benign neoplasm of sweat gland,"['benign tumor of the sweat gland', 'benign sweat gland neoplasm', 'benign tumour of sweat gland', 'benign sweat gland tumor', 'benign neoplasm of the sweat gland', 'sweat gland benign neoplasm', 'benign sweat gland tumour', 'sweat gland neoplasm, benign', 'benign tumor of sweat gland', 'benign tumour of the sweat gland']",,,,C0684354,,C4879,,,,,,
mondo:0021490,benign neoplasm of sebaceous gland,"['sebaceous gland benign neoplasm', 'benign sebaceous gland tumor', 'benign sebaceous neoplasm', 'benign sebaceous gland neoplasm', 'benign sebaceous tumor', 'benign sebaceous skin neoplasm', 'benign tumor of the sebaceous gland', 'benign tumour of the sebaceous gland', 'benign neoplasm of the sebaceous gland', 'benign tumour of sebaceous gland', 'benign tumor of sebaceous gland', 'benign sebaceous skin tumor', 'benign sebaceous skin tumour', 'benign sebaceous gland tumour', 'benign sebaceous tumour']",,,,C0684358,,C8525,,,,,,
mondo:0021491,benign neoplasm of gum,"['benign tumor of the gingiva', 'benign tumour of gingiva', 'benign tumour of the gingiva', 'benign tumor of the gum', 'benign tumour of gum', 'benign gum tumor', 'benign gum tumour', 'benign gum neoplasm', 'benign gingival tumour', 'benign tumor of gingiva', 'benign neoplasm of the gum', 'benign gingival tumor', 'benign gingival neoplasm', 'benign neoplasm of the gingiva', 'benign tumor of gum', 'gingiva benign neoplasm', 'benign neoplasm of gingiva', 'benign tumour of the gum']",,,,C0347201,,C4598,,,210.4,,,
mondo:0021492,benign neoplasm of major salivary gland,"['benign Major salivary gland tumour', 'benign tumor of Major salivary gland', 'benign tumour of the Major salivary gland', 'benign Major salivary gland tumor', 'major salivary gland benign neoplasm', 'benign neoplasm of the Major salivary gland', 'benign Major salivary gland neoplasm', 'benign tumor of the Major salivary gland', 'benign tumour of Major salivary gland']",,,,C0496858,,C4771,,,210.2,,,
mondo:0021493,benign neoplasm of minor salivary gland,"['benign tumor of the minor salivary gland', 'benign neoplasm of the minor salivary gland', 'benign tumour of minor salivary gland', 'benign minor salivary gland neoplasm', 'minor salivary gland benign neoplasm', 'benign tumor of minor salivary gland', 'benign tumour of the minor salivary gland', 'benign minor salivary gland tumor', 'benign minor salivary gland tumour']",,,,C0345615,,C4411,,,210.4,,,
mondo:0021494,benign neoplasm of parotid gland,"['benign parotid tumour', 'benign tumour of parotid gland', 'benign neoplasm of the parotid gland', 'benign tumor of the parotid', 'benign parotid tumor', 'benign neoplasm of parotid', 'benign tumor of parotid', 'benign tumour of the parotid gland', 'benign tumour of parotid', 'benign tumor of the parotid gland', 'benign parotid neoplasm', 'benign neoplasm of the parotid', 'benign parotid gland tumour', 'benign parotid gland neoplasm', 'parotid gland benign neoplasm', 'benign parotid gland tumor', 'benign tumour of the parotid', 'benign tumor of parotid gland']",,,,C0496857,,C4770,,,,D11.0,,
mondo:0021495,benign neoplasm of sublingual gland,"['benign tumour of the sublingual gland', 'benign sublingual gland tumour', 'benign tumor of sublingual gland', 'benign sublingual gland tumor', 'sublingual gland benign neoplasm', 'benign neoplasm of the sublingual gland', 'benign tumour of sublingual gland', 'benign tumor of the sublingual gland', 'benign sublingual gland neoplasm']",,,,C0347208,,C4601,,,,,,
mondo:0021496,benign neoplasm of lip,"['benign Lip tumour', 'benign tumour of the Lip', 'benign tumor of the Lip', 'benign neoplasm of the Lip', 'lip benign neoplasm', 'benign Lip neoplasm', 'benign tumour of Lip', 'benign tumor of Lip', 'benign Lip tumor', 'lip neoplasm, benign']",,,,C0153932,,C3591,,,210.0,D10.0,,
mondo:0021497,benign neoplasm of cerebrum,"['benign tumor of cerebrum', 'benign tumor of cerebral hemispheres', 'benign cerebral hemispheric tumour', 'benign neoplasm of the cerebral hemispheres', 'benign cerebral tumor', 'benign cerebral tumour', 'benign cerebral neoplasm', 'benign tumor of the cerebral hemispheres', 'benign tumor of the cerebrum', 'benign tumour of cerebral hemispheres', 'benign cerebral hemispheric tumor', 'benign tumour of cerebrum', 'benign tumour of the cerebral hemispheres', 'benign neoplasm of cerebral hemispheres', 'benign cerebral hemispheric neoplasm', 'telencephalon benign neoplasm', 'benign neoplasm of the cerebrum', 'benign tumour of the cerebrum']",,,,C0686378,,C8548,,,,,,
mondo:0021498,benign neoplasm of placenta,"['benign placental tumor', 'benign placental tumour', 'benign placenta neoplasm', 'benign tumour of the placenta', 'benign tumor of placenta', 'benign placenta tumor', 'placental neoplasms, benign', 'benign placental neoplasm', 'benign tumor of the placenta', 'benign tumour of placenta', 'benign neoplasm of the placenta', 'benign placenta tumour', 'placenta benign neoplasm']",,,,C0686274,,C8545,,,219.8,,,
mondo:0021499,benign neoplasm of cerebellum,"['benign cerebellar neoplasm', 'neoplasms, cerebellar, benign', 'neoplasms, benign, cerebellar', 'benign tumour of the cerebellum', 'benign cerebellar tumor', 'benign cerebellar neoplasms', 'benign tumor of the cerebellum', 'benign tumor of cerebellum', 'benign tumour of cerebellum', 'cerebellum benign neoplasm', 'benign cerebellar tumour', 'cerebellar neoplasms, benign', 'benign neoplasm of the cerebellum']",,,,,,C4955,,,,,,
mondo:0021500,benign neoplasm of spleen,"['spleen benign neoplasm', 'benign splenic neoplasm', 'benign neoplasm of the spleen']",,,,C0686615,,C4902,,,211.9,,,
mondo:0021501,benign neoplasm of small intestine,"['benign small intestine tumour', 'benign neoplasm of the small intestine', 'small intestine benign neoplasm', 'benign small intestine tumor', 'benign small intestinal tumor', 'benign small intestine neoplasm', 'benign tumour of small intestine', 'benign tumor of the small intestine', 'benign small intestinal neoplasm', 'benign small intestinal tumour', 'benign tumor of small intestine', 'benign tumour of the small intestine']",,,,C0153944,,C3600,,,211.2,,,
mondo:0021503,benign neoplasm of gallbladder,"['gallbladder benign tumor', 'benign tumor of gallbladder', 'benign tumor of the gallbladder', 'benign tumour of gallbladder', 'benign tumour of the gallbladder', 'benign neoplasm of the gallbladder', 'benign gallbladder neoplasm', 'gall bladder benign neoplasm', 'gallbladder benign neoplasm', 'benign gallbladder tumor', 'benign gallbladder tumour', 'gallbladder benign tumour']",0080640,,,C0345912,,C4440,,,,,,
mondo:0021505,benign neoplasm of endocardium,"['benign endocardial tumor', 'benign tumour of endocardium', 'endocardium benign neoplasm', 'benign endocardial tumour', 'benign tumor of endocardium', 'benign tumor of the endocardium', 'benign tumour of the endocardium', 'benign endocardial neoplasm', 'benign neoplasm of the endocardium']",,,,C0347254,,C4608,,,,,,
mondo:0021506,benign neoplasm of spinal cord,"['benign spinal cord tumour', 'benign tumour of the spinal cord', 'benign tumor of the spinal cord', 'spinal cord benign neoplasm', 'benign spinal cord neoplasm', 'benign neoplasm of the spinal cord', 'spinal cord neoplasm, benign', 'benign tumor of spinal cord', 'benign tumour of spinal cord', 'benign spinal cord tumor']",,,,C0154034,,C3627,,,225.3,D33.4,,
mondo:0021507,benign neoplasm of brain stem,"['benign tumor of the brain stem', 'benign tumor of brain stem', 'benign brain stem tumour', 'benign tumour of the brainstem', 'benign neoplasm of the brainstem', 'benign tumors of brainstem', 'benign tumour of the brain stem', 'benign tumor of the brainstem', 'benign neoplasms of the brainstem', 'benign brain stem neoplasms', 'benign tumour of brainstem', 'benign brainstem tumour', 'benign neoplasms of brainstem', 'benign brain stem neoplasm', 'benign tumours of the brainstem', 'benign brainstem tumors', 'benign neoplasm of brainstem', 'benign brainstem neoplasms', 'benign tumour of brain stem', 'brainstem benign neoplasm', 'benign brainstem tumor', 'benign brain stem tumor', 'benign brainstem neoplasm', 'benign tumor of brainstem', 'benign brainstem tumours', 'benign neoplasm of the brain stem', 'benign tumors of the brainstem', 'benign tumours of brainstem']",,,,C0686400,,C8549,,,,,,
mondo:0021508,benign neoplasm of epicardium,"['benign tumor of the epicardium', 'benign tumour of epicardium', 'benign tumor of epicardium', 'benign neoplasm of the epicardium', 'benign epicardial tumour', 'benign epicardial tumor', 'benign tumour of the epicardium', 'epicardium benign neoplasm', 'benign epicardial neoplasm']",,,,C0685115,,C8535,,,,,,
mondo:0021509,benign neoplasm of myocardium,"['benign tumor of the myocardium', 'benign myocardial tumor', 'benign myocardial tumour', 'benign tumour of myocardium', 'benign tumor of myocardium', 'benign neoplasm of the myocardium', 'myocardium benign neoplasm', 'benign tumour of the myocardium', 'benign myocardial neoplasm']",,,,C0347253,,C4607,,,,,,
mondo:0021510,benign neoplasm of prostate,"['benign prostatic neoplasm', 'benign tumor of the prostate', 'benign neoplasm of the prostate', 'benign tumour of prostate', 'benign prostate tumour', 'benign prostate neoplasm', 'benign tumor of prostate', 'prostate gland benign neoplasm', 'benign prostate tumor', 'benign tumour of the prostate']",,,,C0154009,,C3613,,,222.2,D29.1,,
mondo:0021511,benign neoplasm of adrenal gland,"['benign adrenal gland tumour', 'benign tumor of adrenal gland', 'benign adrenal gland tumor', 'benign adrenal tumor', 'benign tumour of adrenal gland', 'benign adrenal gland neoplasm', 'benign tumor of the adrenal gland', 'adrenal gland benign neoplasm', 'benign adrenal tumour', 'benign tumour of the adrenal gland', 'benign adrenal neoplasm', 'benign neoplasm of the adrenal gland']",,,,C0154040,,C3629,,,227.0,,,
mondo:0021512,benign neoplasm of thymus,"['benign neoplasm of the Thymus', 'benign tumour of the Thymus', 'benign thymic tumor', 'benign tumor of Thymus', 'benign Thymus tumour', 'thymus benign neoplasm', 'benign thymic neoplasm', 'benign Thymus tumor', 'benign tumour of Thymus', 'benign Thymus neoplasm', 'benign thymic tumour', 'benign tumor of the Thymus']",,,,C0345975,,C4458,,,212.6,D15.0,,
mondo:0021513,benign neoplasm of tonsil,"['tonsil benign neoplasm', 'benign neoplasm of the tonsil', 'benign tonsil tumour', 'benign tumour of tonsil', 'benign tumor of the tonsil', 'benign tumor of tonsil', 'benign tonsillar neoplasm', 'benign tonsillar tumour', 'benign tonsil neoplasm', 'tonsillar neoplasm, benign', 'benign tonsil tumor', 'benign tonsillar tumor', 'benign tumour of the tonsil']",,,,C0153936,,C3594,,,210.5,D10.4,,
mondo:0021514,benign neoplasm of pericardium,"['benign neoplasm of the pericardium', 'pericardium benign neoplasm', 'benign pericardial tumour', 'benign tumour of pericardium', 'benign tumor of pericardium', 'benign tumour of the pericardium', 'benign pericardial neoplasm', 'benign tumor of the pericardium', 'benign pericardial tumor']",,,,C0685118,,C8536,,,,,,
mondo:0021515,benign neoplasm of ethmoidal sinus,"['benign ethmoid sinus tumour', 'benign tumour of ethmoid sinus', 'benign ethmoidal sinus tumor', 'benign tumor of the ethmoid sinus', 'benign ethmoid sinus tumor', 'benign tumour of ethmoidal sinus', 'benign ethmoidal sinus neoplasm', 'benign neoplasm of the ethmoid sinus', 'benign tumor of ethmoid sinus', 'benign ethmoidal sinus tumour', 'benign tumour of the ethmoid sinus', 'benign tumor of ethmoidal sinus', 'benign neoplasm of the ethmoidal sinus', 'benign tumor of the ethmoidal sinus', 'benign ethmoid sinus neoplasm', 'benign neoplasm of ethmoid sinus', 'ethmoid sinus benign neoplasm', 'benign tumour of the ethmoidal sinus']",,,,C0345670,,C4417,,,212.0,,,
mondo:0021516,benign neoplasm of glottis,"['glottis benign neoplasm', 'benign tumour of glottis', 'benign tumor of the glottis', 'benign glottis neoplasm', 'benign neoplasm of the glottis', 'benign tumour of the glottis', 'benign glottis tumour', 'benign glottis tumor', 'benign tumor of glottis']",,,,C0347234,,C4605,,,,,,
mondo:0021517,benign neoplasm of trachea,"['benign tumour of the trachea', 'benign tumor of trachea', 'benign tracheal neoplasm', 'benign trachea tumor', 'benign neoplasm of the trachea', 'benign tracheal tumour', 'trachea benign neoplasm', 'benign tumor of the trachea', 'benign trachea tumour', 'benign tracheal tumor', 'benign tumour of trachea', 'benign trachea neoplasm']",,,,C0153953,,C3602,,,212.2,D14.2,,
mondo:0021518,benign neoplasm of hard palate,"['benign hard palate neoplasm', 'benign hard palate tumour', 'hard palate benign neoplasm', 'benign tumor of hard palate', 'benign neoplasm of the hard palate', 'benign tumour of the hard palate', 'benign hard palate tumor', 'benign tumor of the hard palate', 'benign tumour of hard palate']",,,,C0345552,,C4403,,,210.4,,,
mondo:0021520,benign neoplasm of floor of mouth,"['benign tumor of the floor of the mouth', 'benign tumour of the floor of the mouth', 'benign floor of mouth tumor', 'benign floor of mouth neoplasm', 'benign neoplasm of the floor of the mouth', 'benign tumour of floor of mouth', 'benign floor of the mouth neoplasm', 'mouth floor benign neoplasm', 'benign tumor of floor of mouth', 'benign floor of the mouth tumour', 'benign floor of the mouth tumor', 'benign floor of mouth tumour']",,,,C0153934,,C3593,,,210.3,D10.2,,
mondo:0021521,benign neoplasm of mediastinum,"['benign tumour of the mediastinum', 'benign tumor of mediastinum', 'benign mediastinal tumour', 'benign tumour of mediastinum', 'benign mediastinal neoplasm', 'benign tumor of the mediastinum', 'benign neoplasm of the mediastinum', 'mediastinum benign neoplasm', 'benign mediastinal tumor']",,,,C0153956,,C3604,,,212.5,D15.2,,
mondo:0021522,benign neoplasm of lower jaw bone,['bone of lower jaw benign neoplasm'],,,,C0004994,,C34417,,,213.1,D16.5,,
mondo:0021523,benign neoplasm of pharynx,"['benign pharynx tumour', 'benign pharynx neoplasm', 'benign pharyngeal tumour', 'benign tumour of the pharynx', 'pharyngeal neoplasm benign', 'benign tumor of pharynx', 'benign tumour of pharynx', 'benign pharynx tumor', 'pharynx benign neoplasm', 'benign pharyngeal neoplasm', 'benign neoplasm of the pharynx', 'benign tumor of the pharynx', 'benign pharyngeal tumor']",,,,C0153940,,C3597,,,210.9,,,
mondo:0021524,benign neoplasm of buccal mucosa,"['benign neoplasm of the buccal mucosa', 'benign tumor of the buccal mucosa', 'benign buccal mucosa tumor', 'benign tumour of the buccal mucosa', 'buccal mucosa benign neoplasm', 'benign tumour of buccal mucosa', 'benign buccal mucosa neoplasm', 'benign buccal mucosa tumour', 'benign tumor of buccal mucosa']",,,,C0345566,,C4406,,,210.4,,,
mondo:0021525,benign neoplasm of corpus uteri,"['benign tumour of the body of uterus', 'benign uterine body tumour', 'benign tumor of the corpus uteri', 'benign neoplasm of uterine corpus', 'benign uterine corpus tumour', 'benign tumour of the corpus uteri', 'benign corpus uteri tumor', 'benign neoplasm of the body of uterus', 'benign tumour of uterine corpus', 'benign neoplasm of the uterine body', 'benign tumor of the uterine corpus', 'benign tumour of body of uterus', 'benign tumour of corpus uteri', 'benign uterine body neoplasm', 'benign neoplasm of the corpus uteri', 'benign tumor of corpus uteri', 'benign corpus uteri tumour', 'benign neoplasm of uterine body', 'benign tumour of the uterine body', 'benign uterine corpus neoplasm', 'benign tumor of uterine body', 'benign tumor of the uterine body', 'benign corpus uteri neoplasm', 'benign neoplasm of the uterine corpus', 'benign uterine body tumor', 'body of uterus benign neoplasm', 'benign tumour of uterine body', 'benign tumour of the uterine corpus', 'benign tumor of the body of uterus', 'benign tumor of body of uterus', 'benign tumor of uterine corpus', 'benign uterine corpus tumor', 'benign neoplasm of body of uterus']",,,,C0153998,,C3608,,,219.1,,,
mondo:0021527,benign neoplasm of meninges,"['benign meningeal tumours', 'benign meningeal neoplasms', 'benign meningeal tumor', 'benign tumor of the meninges', 'benign neoplasms of meninges', 'meningeal cluster benign neoplasm', 'benign meninges neoplasm', 'meningeal tumors, benign', 'benign meninges tumor', 'benign tumour of the meninges', 'benign meningeal neoplasm', 'benign meningeal tumors', 'benign tumor of meninges', 'benign neoplasm of the meninges', 'benign neoplasms of the meninges', 'benign tumour of meninges', 'benign meninges tumour', 'benign meningeal tumour']",,,,C0348426,,C4957,,,,D32,,
mondo:0021528,benign neoplasm of male breast,"['benign Male breast tumour', 'benign tumour of the Male breast', 'benign Male breast tumor', 'male breast benign neoplasm', 'benign neoplasm of the Male breast', 'benign tumor of Male breast', 'benign Male breast neoplasm', 'benign tumour of Male breast', 'benign tumor of the Male breast']",,,,C0347482,,C4620,,,,,,
mondo:0021529,benign neoplasm of chest wall,"['benign neoplasm of the chest wall', 'benign tumor of the chest wall', 'benign chest wall tumor', 'chest wall benign neoplasm', 'benign tumor of chest wall', 'benign chest wall neoplasm', 'benign tumour of chest wall', 'benign tumour of the chest wall', 'benign chest wall tumour']",,,,C0684831,,C8529,,,229.8,,,
mondo:0021530,benign neoplasm of subglottis,"['benign subglottic neoplasm', 'benign subglottic tumor', 'benign subglottis tumour', 'subglottis benign neoplasm', 'benign tumor of the subglottis', 'benign neoplasm of the subglottis', 'benign tumour of the subglottis', 'benign subglottic tumour', 'benign tumor of subglottis', 'benign subglottis tumor', 'benign tumour of subglottis', 'benign subglottis neoplasm']",,,,C0345749,,C4427,,,,,,
mondo:0021531,fibroma of lung,"['pulmonary fibroma', 'lung fibroma', 'fibroma of the lung']",,,,C1334444,,C5658,,,,,,
mondo:0021532,fibroma of prostate,"['fibroma of the prostate', 'prostate fibroma', 'prostate gland fibroma']",,,,C0268885,,C3972,,,600.20,,,
mondo:0021533,intestinal neuroendocrine tumor G1,"['intestinal carcinoid tumor', 'carcinoid tumor of intestine', 'carcinoid tumour of the intestine', 'grade 1 neuroendocrine neoplasm of intestine', 'intestine carcinoid tumor (disease)', 'intestine NET G1', 'intestine neuroendocrine tumor, well differentiated, low grade', 'intestine carcinoid tumor', 'carcinoid tumour of intestine', 'carcinoid tumor of the intestine', 'intestinal NET G1', 'intestinal carcinoid tumour', 'intestinal neuroendocrine tumor G1', 'intestine carcinoid tumour (disease)', 'intestine carcinoid tumour']",,114900,,C0349535,,C4637,,C562842,,,,
mondo:0021534,rectal neuroendocrine tumor G1,"['carcinoid tumour of rectum', 'grade 1 neuroendocrine neoplasm of rectum', 'rectum NET G1', 'carcinoid tumor of rectum', 'rectal carcinoid', 'carcinoid tumor of the rectum', 'rectum neuroendocrine tumor, well differentiated, low grade', 'rectal carcinoid tumor', 'rectum carcinoid tumour', 'rectum carcinoid tumour (disease)', 'carcinoid of rectum', 'rectal NET G1', 'rectal neuroendocrine tumor G1', 'rectal carcinoid tumour', 'carcinoid of the rectum', 'rectum carcinoid tumor', 'rectum carcinoid tumor (disease)', 'carcinoid tumour of the rectum']",,,,C1335678,,C5547,,,,,,
mondo:0021535,pancreatic neuroendocrine tumor G1,"['pancreas carcinoid tumour', 'pancreas neuroendocrine tumor, well differentiated, low grade', 'pancreatic NET G1', 'pancreatic neuroendocrine tumor G1', 'pancreas NET G1', 'pancreas carcinoid tumor', 'grade 1 neuroendocrine neoplasm of pancreas']",,,,,,C95584,,,,,,
mondo:0021537,undifferentiated carcinoma of nasopharynx,"['nasopharynx undifferentiated carcinoma', 'nasopharyngeal undifferentiated carcinoma', 'nasopharyngeal nonkeratinizing undifferentiated carcinoma', 'nasopharyngeal lymphoepithelioma', 'lymphoepithelioma of nasopharynx', 'undifferentiated carcinoma of the nasopharynx', 'undifferentiated nasopharyngeal throat cancer', 'lymphoepithelioma of the nasopharynx']",,,,C0279748,,C8023,,,,,,
mondo:0021538,verrucous carcinoma of oral cavity,"['mouth verrucous carcinoma', 'verrucous carcinoma of mouth', 'oral cavity verrucous carcinoma', 'verrucous carcinoma of the mouth', 'verrucous carcinoma of the oral cavity', 'oral cavity verrucous cancer']",,,,C0280306,,C8174,,,,,,
mondo:0021539,hamartoma of skin appendage,"['skin appendage hamartoma', 'cutaneous appendage hamartoma (disease)']",,,,C1302712,,C5562,,,759.6,,,
mondo:0021540,hamartoma of lung,"['hamartoma of the lung', 'lung hamartoma (disease)', 'lung hamartoma', 'lung chondroid hamartoma', 'pulmonary hamartoma']",,,,C0149927,,C3497,,,235.7,,,
mondo:0021541,hemangioma of retina,"['retina hemangioma', 'retina angioma', 'retinal hemangioma', 'retinal angioma', 'hemangioma of the retina', 'angioma of the retina', 'angioma of retina']",,,,C0154051,,C3634,,,228.03,,,
mondo:0021542,hemangioma of choroid,"['angioma of the choroid', 'hemangioma of the choroid', 'choroid hemangioma', 'hemangioma, choroid, benign', 'optic choroid hemangioma', 'choroid angioma', 'benign choroid angioma', 'benign choroid hemangioma', 'hemangioma of optic choroid', 'angioma of choroid', 'benign hemangioma of the choroid', 'benign hemangioma of choroid', 'benign angioma of choroid', 'benign angioma of the choroid']",,,,C0346390,,C4562,,,228.09,,,
mondo:0021543,hemangioma of gingiva,"['gingival hemangioma', 'gingiva hemangioma', 'angioma of gum', 'gingival angioma', 'hemangioma of the gum', 'gum hemangioma', 'gum angioma', 'angioma of the gingiva', 'hemangioma of the gingiva', 'angioma of the gum', 'hemangioma of gum', 'angioma of gingiva']",,,,C0582885,,C4831,,,228.09,,,
mondo:0021545,myomatous neoplasm,"['muscle tumour', 'muscle tissue neoplasms', 'myoblastomas', 'myofibroblastomas', 'tumour of the muscle', 'muscle tumor', 'tumor of muscle', 'tumour of muscle', 'myomatous neoplasm', 'tumor of the muscle', 'myofibroblastoma', 'neoplasm, muscle tissue', 'myoblastoma', 'muscle neoplasm', 'myomatous tumour', 'myomatous tumor', 'neoplasm of the muscle', 'muscle tissue neoplasm', 'neoplasm of muscle']",,,,,,C4063,,D019042,,,,
mondo:0021546,ependymal tumor of spinal cord,"['ependymal tumor of spinal cord', 'spinal cord ependymal tumour', 'spinal cord ependymal tumor']",,,,C4318747,,C131526,,,,,,
mondo:0021547,amelogenesis imperfecta type 3B,"['AI3B', 'amelogenesis imperfecta, type 3B', 'amelogenesis imperfecta, type IIIB']",0080243,617607,,CN373594,,,,,,,,
mondo:0021548,total early-onset cataract,"['cataract, total congenital', 'CCT', 'cataract, total congenital with posterior sutural opacities in heterozygotes']",,,98994,,,,,,,,,
mondo:0021553,transverse myelitis,"['Myelitis, Transverse', 'Transverse myelitis', 'Transverse Myelopathy Syndrome', 'Transverse myelopathy syndrome', 'Transverse Myelopathy Syndromes', 'Transverse Myelitis']",0080743,,,C0026976,,,,,323.9,,10028527,
mondo:0021559,non-autoimmune hemolytic anemia,"['non-autoimmune hemolytic anemia', 'Non-autoimmune hemolytic anaemia', 'Non-autoimmune hemolytic anemia', 'Non-Autoimmune Hemolytic Anemia', 'Non-Autoimmune Hemolytic Anaemia']",,,,C0028283,,C34853,,,283.19,,,
mondo:0021562,omphalitis,"['omphalitis', 'Omphalitis']",,,,C0028992,,C116008,,,,,,
mondo:0021568,renal tubule disorder,"['renal tubule disease or disorder', 'renal tubular disorder', 'disease of renal tubule', 'renal tubule disease', 'renal tubular disease', 'disorder of renal tubule']",,,,C0151747,,,,,588.89,,,
mondo:0021569,"Emery-Dreifuss muscular dystrophy 2, autosomal dominant","['EDMD2', 'limb-girdle muscular dystrophy due to lamin A/C deficiency', 'autosomal dominant limb-girdle muscular dystrophy caused by mutation in LMNA', 'Emery-Dreifuss muscular dystrophy, autosomal dominant', 'scapuloilioperoneal atrophy with cardiopathy', 'muscular dystrophy, limb-girdle type 1B', 'muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant', 'limb-girdle muscular dystrophy type 1B', 'autosomal dominant limb-girdle muscular dystrophy type 1B', 'EMD2', 'LGMD1B', 'muscular dystrophy, proximal, type 1B', 'muscular dystrophy, limb-girdle, type 1B', 'benign scapuloperoneal muscular dystrophy with cardiomyopathy', 'proximal muscular dystrophy type 1B', 'LMNA autosomal dominant limb-girdle muscular dystrophy', 'Hauptmann-Thannhauser muscular dystrophy', 'Emery-Dreifuss muscular dystrophy 2, autosomal dominant']",0110301,181350,98853,C2750035,"['0.03555', '-0.713', '-0.3018', '-0.2034', '0.4656', '-1.186', '0.1221', '0.4326', '-1.774', '-0.922', '-0.07306', '0.1935', '-0.2747', '1.254', '0.3308', '0.309', '-0.7163', '-0.2644', '-0.3694', '-0.508', '-0.1624', '0.387', '0.2686', '0.3694', '0.2018', '-0.4033', '0.002897', '-0.8447', '0.187', '-0.304', '0.708', '-0.2428', '0.638', '0.1976', '0.2532', '0.09644', '-0.8296', '0.1687', '0.29', '-0.5713', '-0.01721', '-0.2316', '-0.2357', '0.4307', '0.0304', '0.1895', '-0.0899', '0.7954', '0.0982', '0.3083', '0.366', '-0.53', '0.2136', '-0.7344', '0.08606', '-0.3357', '0.3223', '1.107', '-0.2783', '0.1338', '-0.006706', '0.0374', '-0.05975', '-0.1837', '-0.002512', '0.02458', '0.1747', '0.5317', '-0.3418', '0.09644', '-0.0875', '0.2379', '0.10474', '-0.501', '0.9004', '0.706', '-0.4753', '0.3516', '-0.2893', '0.02626', '0.1293', '-0.1932', '-0.2651', '0.07416', '-0.3228', '0.118', '-0.09344', '-0.3738', '0.9614', '0.28', '-0.4517', '-0.1153', '0.2512', '0.957', '-0.0772', '0.308', '0.301', '-0.5767', '0.0798', '-0.187']",C126745,,C535898,425.4,,,
mondo:0021571,"multiple sclerosis, susceptibility to 1","['MS1', 'MS', 'multiple sclerosis, disease progression, modifier of', 'multiple sclerosis, susceptibility to, 1', 'multiple sclerosis, susceptibility to', 'susceptibility to multiple sclerosis', 'disseminated sclerosis']",,126200,,CN031763,,,,,,,,
mondo:0021573,oocyte maturation defect 2,"['TUBB8 inherited oocyte maturation defect', 'inherited oocyte maturation defect caused by mutation in TUBB8', 'oocyte maturation defect 2', 'OOMD2']",,616780,488191,C4225210,,,,,,,,
mondo:0021574,oocyte maturation defect 3,"['oocyte maturation defect 3', 'OOMD3']",,617712,404466,,,,,,,,,
mondo:0021575,oocyte maturation defect 4,"['OOMD4', 'oocyte maturation defect 4']",,617743,488191,CN562785,,,,,,,,
mondo:0021576,fallopian tube endometrioid tumor,"['fallopian tube endometrioid tumor', 'endometrium neoplasm of fallopian tube', 'fallopian tube endometrioid neoplasm', 'fallopian tube endometrium neoplasm']",,,,C1517113,,C40111,,,,,,
mondo:0021577,malignant mediastinal neural neoplasm,,,,,C0349665,,,,,,,,
mondo:0021578,sternal neoplasm,"['tumour of the sternum', 'sternal tumor', 'sternal tumour', 'tumor of the sternum', 'sternum tumor', 'tumour of sternum', 'tumor of sternum', 'sternal neoplasm', 'neoplasm of sternum', 'sternum neoplasm (disease)', 'neoplasm of the sternum', 'sternum tumour']",,,,C1290244,,C6730,,,239.2,,,
mondo:0021579,neoplasm of femur,"['tumor of femur', 'neoplasm of femur', 'femur tumor', 'femur neoplasm (disease)', 'tumour of femur', 'femur tumour']",,,,,,,,,239.2,,,
mondo:0021580,neoplasm of jaw,"['jaw skeleton neoplasm (disease)', 'tumor of jaw skeleton', 'jaw skeleton tumor', 'jaw skeleton tumour', 'tumour of jaw skeleton', 'neoplasm of jaw skeleton']",,,,,,,,,239.89,,,
mondo:0021581,connective tissue neoplasm,"['neoplasm of connective tissues', 'neoplasm, connective tissue', 'tumour of connective tissue', 'connective tissue tumour', 'tumor of connective tissue', 'neoplasm of connective tissue', 'connective tissue neoplasm (disease)', 'connective tissue neoplasms', 'connective tissue tumor', 'connective tissue neoplasm']",,,,C0027656,,,,D009372,239.2,,,
mondo:0021582,lentigo,"['lentigo', 'lentiginosis', 'lentigines']",,150900,,,,C3159,,D007911,,,,
mondo:0021583,melanocytic skin neoplasm,"['cutaneous melanocytic neoplasm', 'zone of skin melanocytic neoplasm', 'melanocytic neoplasm of skin', 'melanocytic skin neoplasm', 'melanocytic neoplasm of zone of skin']",,,,C0349501,,C7161,,,,,,
mondo:0021588,eyelid sebaceous gland carcinoma,"['carcinoma of sebaceous gland of eyelid', 'sebaceous gland carcinoma of the eyelid', 'eyelid sebaceous gland carcinoma', 'eyelid SGC', 'sebaceous gland of eyelid carcinoma']",,,,C4525405,,C134831,,,,,,
mondo:0021605,benign eyelid neoplasm,"['benign tumour of the eyelid', 'benign tumor of eyelid', 'benign neoplasm of eyelid', 'benign tumor of the eyelid', 'benign tumour of eyelid', 'benign eyelid tumor', 'benign eyelid neoplasm', 'eyelid benign neoplasm', 'benign eyelid tumour', 'benign neoplasm of the eyelid']",,,,C0339107,,C4354,,,,,,
mondo:0021607,eyelid seborrheic keratosis,"['basal cell papilloma of eyelid', 'basal cell papilloma of the eyelid', 'eyelid seborrheic keratosis', 'seborrheic keratosis of the eyelid', 'eyelid basal cell papilloma', 'seborrheic keratosis of eyelid']",,,,C0339109,,C4356,,,,,,
mondo:0021627,eyelid capillary hemangioma,"['capillary angioma of the eyelid', 'eyelid capillary hemangioma', 'capillary angioma of lid', 'eyelid capillary angioma', 'capillary hemangioma of the lid', 'capillary hemangioma of lid', 'capillary hemangioma of the eyelid', 'capillary hemangioma of eyelid', 'capillary angioma of the lid', 'capillary angioma of eyelid']",,,,C0339110,,C4357,,,,,,
mondo:0021629,uterine ligament neoplasm,"['tumour of uterine ligament', 'neoplasm of the uterine ligament', 'uterine ligament neoplasm (disease)', 'tumor of the uterine ligament', 'uterine ligament tumor', 'uterine ligament neoplasm', 'tumor of uterine ligament', 'neoplasm of uterine ligament', 'uterine ligament tumour', 'tumour of the uterine ligament']",,,,C1519870,,C40133,,,,,,
mondo:0021630,lipoma of face,['face lipoma'],,,,,,,,,214.0,,,
mondo:0021631,brain astrocytoma,"['astrocytoma (excluding glioblastoma) of brain', 'brain astrocytoma', 'brain astrocytoma (excluding glioblastoma)']",,,,C3695127,,C60780,,,,,,
mondo:0021632,primary brain neoplasm,"['primary brain tumor', 'primary brain tumour', 'primary brain neoplasm']",,,,,,C4952,,,,,,
mondo:0021633,cerebral astrocytoma,"['astrocytoma of cerebrum', 'astrocytoma of the cerebral hemispheres', 'cerebral hemisphere astrocytoma (excluding glioblastoma)', 'astrocytoma of the cerebrum', 'astrocytoma (excluding glioblastoma) of cerebral hemisphere', 'astrocytoma of cerebral hemispheres', 'cerebral hemispheric astrocytoma', 'cerebral astrocytoma']",,,,,,C4951,,,,,,
mondo:0021634,epithelial skin neoplasm,"['skin epithelium neoplasm', 'skin epithelium tumour', 'epithelial skin tumor', 'zone of skin epithelial neoplasm', 'skin epithelium tumor', 'epithelial skin tumour', 'epithelial skin neoplasm']",,,,C0345976,,C7342,,,,,,
mondo:0021635,neurocristopathy,"['disorder of neural crest cell development', 'disorder of neural crest development']",,,,,,,,,,,,
mondo:0021636,astrocytic tumor,"['astrocytic tumor', 'astrocytoma of cerebrum', 'astrocytoma of brain', 'astroglioma', 'astrocytic neoplasm', 'astrocytoma, no ICD-O subtype', 'astrocytoma']",3069,,94,,,C6958,0000272,,,,10003571,
mondo:0021637,low grade glioma,"['low-grade glioma', 'low grade glioma']",0080829,,,C1997217,,C132067,,,,,,
mondo:0021638,low grade astrocytic tumor,"['low-grade astrocytic tumour', 'low grade astrocytic tumor', 'low-grade astrocytic neoplasm', 'low grade astrocytic neoplasm', 'low-grade astrocytic tumor']",,,,C3898569,,C116342,,,,,,
mondo:0021639,grade II glioma,"['grade II glioma', 'WHO grade II glioma']",,,,C4330050,,C132505,,,,,,
mondo:0021640,grade III glioma,"['WHO grade III glioma', 'anaplastic glioma']",,,,C4287997,,C127816,,,,,,
mondo:0021641,Bunyaviridae infectious disease,"['Bunyaviridae infectious disease', 'infections, Bunyaviridae', 'Bunyaviridae infection', 'Bunyavirus infection', 'Bunyavirus infections', 'infections, Bunyavirus', 'Bunyaviridae caused disease or disorder']",,,,,,,0007188,D002044,,,,
mondo:0021642,vulval varices,"['mammalian vulva varicose disease', 'varicose disease of mammalian vulva']",,,,C0155796,,,,,456.6,I86.3,,0100677
mondo:0021643,mesenteric varices,"['mesentery varicose disease', 'varicose disease of mesentery']",,,,,,,,,,,,0002626
mondo:0021644,esophageal varices without bleeding,,,,,C0267092,,,,,456.1,I85.00,,
mondo:0021645,esophageal varices with bleeding,,,,,,,,,,456.0,I85.01,,
mondo:0021650,uterine corpus neuroendocrine neoplasm,"['body of uterus neuroendocrine tumour', 'uterine corpus neuroendocrine tumor', 'body of uterus NET', 'neuroendocrine neoplasm of body of uterus', 'body of uterus neuroendocrine neoplasm', 'uterine corpus neuroendocrine neoplasm', 'body of uterus neuroendocrine tumor, well differentiated, low or intermediate grade', 'body of uterus neuroendocrine tumor', 'uterine corpus neuroendocrine tumour']",,,,C4288048,,C126771,,,,,,
mondo:0021651,synpolydactyly,"['syndactyly type 2', 'polysyndactyly', 'SPD', 'synpolydactyly']",,,93403,C0265553,"['-0.1378', '-0.106', '0.0709', '-0.2465', '0.1726', '-0.3804', '0.004944', '0.1901', '-0.4583', '-0.4214', '-0.1965', '-0.01187', '-0.096', '0.1586', '-0.1154', '-0.002823', '0.1243', '-0.3367', '0.0416', '-0.439', '-0.1799', '0.00554', '0.2627', '-0.08624', '0.4607', '0.2805', '-0.1082', '0.1858', '0.07947', '-0.2673', '0.3123', '-0.1371', '0.09827', '0.1575', '0.264', '-0.1558', '0.097', '-0.2874', '-0.03372', '-0.11426', '0.0677', '-0.255', '0.1582', '0.2046', '0.1812', '-0.26', '-0.1202', '0.4724', '0.01567', '-0.02194', '-0.06525', '-0.0587', '-0.04074', '-0.1747', '-0.2507', '-0.4111', '0.144', '-0.1501', '-0.1636', '-0.1197', '0.2942', '0.03595', '0.0491', '0.2969', '-0.1877', '-0.03436', '0.05814', '0.1904', '-0.128', '0.1418', '-0.499', '0.06445', '0.2386', '-0.08325', '0.3713', '0.257', '0.003944', '-0.0688', '-0.3567', '-0.4084', '-0.1956', '0.03156', '0.3242', '0.1884', '0.03314', '0.06354', '-0.2744', '0.2546', '0.1274', '-0.3865', '-0.1675', '0.3423', '0.2488', '0.01987', '0.545', '-0.0874', '0.5537', '-0.602', '0.246', '0.2471']",C75003,,C538153,,,,
mondo:0021652,diffuse type adenocarcinoma,"['diffuse type adenocarcinoma', 'diffuse type carcinoma']",,,,,,C4127,,,,,,
mondo:0021653,cutaneous focal mucinosis,,,,,C0406659,,,,,701.8,,,
mondo:0021654,diffuse cutaneous mucinosis,,,,,C0406655,,,,,701.8,,,
mondo:0021655,secondary catabolic mucinosis of skin,,,,,C1274173,,,,,701.8,,,
mondo:0021656,nongerminomatous germ cell tumor,"['non-germinomatous germ cell tumour', 'non-germinomatous germ cell tumor', 'non-seminomatous germ cell tumor', 'Nongerminomatous germ cell tumour', 'non-dysgerminomatous germ cell tumor', 'non-seminomatous germ cell tumour', 'Nongerminomatous germ cell tumor Including central nervous system', 'Nongerminomatous germ cell tumor', 'Nongerminomatous germ cell tumour Including central nervous system', 'non-dysgerminomatous germ cell tumour', 'NSGCT']",,,,,,C121619,,,,,,
mondo:0021657,ovarian sex cord-stromal tumor,"['sex cord stromal tumor', 'Sex cord-stromal neoplasm of ovary', 'Sex cord-stromal tumour of ovary', 'sex cord-stromal tumour of ovary', 'Sex cord-stromal tumor of ovary', 'ovarian Sex cord-stromal tumor', 'Sex cord-stromal tumour of the ovary', 'ovarian Sex cord-stromal tumour', 'Sex cord-stromal neoplasm of the ovary', 'ovary sex cord-stromal tumor', 'ovarian sex cord tumor with annular tubules', 'ovarian sex cord tumour with annular tubules', 'sex cord stromal tumour', 'ovarian Sex cord-stromal neoplasm', 'ovary sex cord-stromal tumour', 'Sex cord-stromal tumor of the ovary']",0080369,,,C0600113,,C4862,1000430,,,,,
mondo:0021658,vascular ectasia,['vascular ectasia'],,,,C0002959,,C45481,,,,,,
mondo:0021659,combined carcinoid and adenocarcinoma,"['adenocarcinoid tumour', 'mixed carcinoid neoplasm', 'adenocarcinoid neoplasm', 'adenocarcinoid tumor', 'mixed carcinoid tumour', 'combined carcinoid neoplasm and adenocarcinoma', 'combined carcinoid and adenocarcinoma', 'composite carcinoid neoplasm', 'composite carcinoid tumour', 'combined carcinoid tumor and adenocarcinoma', 'combined carcinoid tumour and adenocarcinoma', 'composite carcinoid', 'composite carcinoid tumor', 'mixed carcinoid tumor']",,,,C0334302,,C4139,,C538230,,,,
mondo:0021660,deep seated dermatophytosis,"['deep seated dermatophytosis', 'disseminated granulomatous dermatophytosis', 'deep dermatophytosis']",,,397587,C1395264,,C35073,,,,,,
mondo:0021661,coronary atherosclerosis,"['coronary artery arteriosclerosis disorder', 'coronary artery arteriosclerosis (disease)', 'arteriosclerosis disorder of coronary artery', 'coronary atherosclerosis']",,,,,,C35505,,,414.00,,,
mondo:0021662,bile duct neoplasm,"['bile duct tumour', 'tumor of bile duct', 'neoplasm of bile duct', 'bile duct tumor', 'intrahepatic and extrahepatic bile duct neoplasm', 'bile duct neoplasm (disease)', 'tumour of bile duct', 'intrahepatic and extrahepatic bile duct tumour', 'intrahepatic and extrahepatic bile duct tumor', 'bile duct neoplasm']",,,,C0005396,,C2898,,D001650,,,,
mondo:0021663,sarcomatoid squamous cell carcinoma,"['squamous cell carcinoma, sarcomatoid', 'squamous cell spindle cell carcinoma', 'epidermoid spindle cell carcinoma', 'sarcomatoid squamous cell carcinoma', 'squamous cell carcinoma, spindle cell', 'spindle cell (sarcomatoid) squamous cell carcinoma']",,,,,,C27084,,,199.1,,,
mondo:0021666,ear infection,"['Ear infection', 'otitis']",,,,C0699744,,C27193,,D010031,,,,
mondo:0021667,neuralgia,"['paroxysmal nerve pain', 'pain, nerve', 'pain, neuropathic', 'paroxysmal nerve pains']",,,,,,,,D009437,729.2,,,
mondo:0021669,post-infectious disorder,['sequela of infectious disorder'],,,,,,,,,139.8,B90-B94,,
mondo:0021670,post-infectious syndrome,,,,,,,,,,,,,
mondo:0021673,post-bacterial disorder,,,,,,,,,,,,,
mondo:0021674,post-viral disorder,['sequela of viral disease'],,,,,,,,,139.8,,,
mondo:0021677,post-infectious neuralgia,,,,,C0032772,,,,,729.2,,,
mondo:0021678,gram-negative bacterial infections,"['gramme negative bacterial infections', 'gram-negative bacterial infection', 'gram negative bacterial infections', 'bacterial infections, gramme negative', 'bacterial infections, gram-negative', 'bacterial infection, gram-negative', 'infection, gram-negative bacterial', 'infections, gram-negative bacterial', 'infections, gramme negative bacterial', 'infections, gram negative bacterial', 'bacterial infections, gram negative']",,,,,,,,D016905,041.85,,,
mondo:0021679,gram-positive bacterial infections,"['infections, Gram Positive bacterial', 'Gram-positive bacterial infection', 'infections, Gramme Positive bacterial', 'Gramme Positive bacterial infections', 'bacterial infections, Gram Positive', 'infections, Gram-positive bacterial', 'bacterial infections, Gram-positive', 'bacterial infections, Gramme Positive', 'Gram Positive bacterial infections', 'infection, Gram-positive bacterial', 'bacterial infection, Gram-positive']",,,,,,,,D016908,041.89,,,
mondo:0021680,streptococcal infection,"['Streptococcus caused disease or disorder', 'infections, streptococcal', 'streptococcal infection', 'infection, streptococcal']",,,,C0038395,,C87062,1001476,D013290,041.09,,,
mondo:0021681,sexually transmitted disease,"['disease (VD), venereal', 'infections, sexually Transmitted', 'disease, venereal', 'infection, sexually Transmitted', 'STD', 'VD, venereal disease', 'venereal disease', 'Transmitted infection, sexually', 'Transmitted infections, sexually', 'diseases, sexually Transmitted', 'sexually transmitted disease', 'STIs', 'disease, sexually Transmitted', 'venereal diseases', 'diseases, venereal', 'STDs', 'VD', 'sexually Transmitted infection', 'sexually Transmitted infections', 'STI', 'venereal disease (VD)', 'sexually Transmitted disorder']",,,,C0036916,,C3365,,D012749,099.9,A50-A64,,
mondo:0021682,viral sexually transmitted disease,"['disease, viral venereal', 'sexually Transmitted disease, viral', 'viral venereal diseases', 'venereal disease, viral', 'diseases, viral venereal', 'viral venereal disease', 'viral sexually Transmitted diseases', 'venereal diseases, viral', 'viral sexually transmitted disease']",,,,C0036918,,,,D015229,,,,
mondo:0021697,chlamydia infectious disease,"['infections, Chlamydia', 'Chlamydia infection', 'Chlamydophila caused disease or disorder', 'Chlamydia caused disease or disorder', 'infection, Chlamydia']",,,,,,,1000863,D023521,,A70-A74,,
mondo:0021698,alcohol-related disorders,"['disorder, alcohol-related', 'alcohol-related disorder', 'alcohol related disorders', 'disorders, alcohol-related']",,,,,,,,D019973,,,,
mondo:0021699,alcohol-induced disorders,"['alcohol induced disorders', 'alcohol-induced disorder']",,,,C0236970,,,,D020751,,,,
mondo:0021702,alcohol amnestic disorder,"['syndrome, alcohol-induced Korsakoff', 'syndromes, alcohol-induced Dysmnesic', 'amnestic syndrome, alcohol-induced', 'psychosis, alcohol-induced amnestic', 'syndromes, alcohol-induced amnestic', 'syndromes, alcohol-induced Korsakoff', 'psychoses, alcohol-induced Dysmnesic', 'Dysmnesic psychosis, alcohol-induced', 'Korsakoff syndromes, alcohol-induced', 'Dysmnesic syndrome, alcohol-induced', 'alcoholic Korsakoff syndrome', 'syndromes, alcoholic Korsakoff', 'alcohol induced amnestic syndrome', 'alcohol-induced Korsakoff syndrome', 'alcohol amnestic syndrome', 'alcohol-induced Dysmnesic psychoses', 'alcohol-induced persisting amnestic disorder', 'amnestic psychosis, alcohol induced', 'psychoses, alcohol-induced amnestic', 'alcohol induced persisting amnestic disorder', 'Korsakoff syndromes, alcoholic', 'amnestic syndromes, alcohol', 'alcohol-induced Dysmnesic syndrome', 'alcohol amnestic disorders', 'alcohol-induced amnestic syndromes', 'alcohol-induced amnestic psychosis', 'syndrome, alcohol-induced amnestic', 'alcohol induced amnestic psychosis', 'psychosis, alcohol-induced Dysmnesic', 'amnestic syndrome, alcohol', 'Korsakoff syndrome, alcohol-induced', 'Dysmnesic psychoses, alcohol-induced', 'alcohol-induced Dysmnesic syndromes', 'syndromes, alcohol amnestic', 'alcohol-induced Dysmnesic psychosis', 'amnestic psychoses, alcohol-induced', 'alcohol-induced Korsakoff syndromes', 'syndrome, alcohol amnestic', 'alcohol amnestic syndromes', 'amnestic disorders, alcohol', 'alcohol induced Korsakoff syndrome', 'amnestic disorder, alcohol', 'syndrome, alcoholic Korsakoff', 'alcohol induced Dysmnesic syndrome', 'amnestic syndromes, alcohol-induced', 'syndrome, alcohol-induced Dysmnesic', 'Dysmnesic syndromes, alcohol-induced', 'alcohol induced Dysmnesic psychosis', 'Korsakoff syndrome, alcoholic', 'amnestic psychosis, alcohol-induced', 'alcoholic Korsakoff syndromes', 'alcohol-induced amnestic syndrome', 'alcohol-induced amnestic psychoses']",,,,,,,1001759,D000425,,,,
mondo:0021718,polyneuritis,"['Polyneuritides', 'Inflammatory polyneuropathy', 'polyneuritis', 'Polyneuritis', 'Multiple neuritis']",,,,C0032541,,C26864,,,,,,0031003
mondo:0021722,vulvodynia,,,,,,,,,D056650,625.70,,,
mondo:0021723,vaginismus,"['vaginismus', 'myalgia of pelvic floor']",,,,C2004487,,,,D052065,,N94.2,,
mondo:0021726,abdominal cystic lymphangioma,"['abdominal retroperitoneal lymphangioma', 'RCL', 'abdomen cystic lymphangioma', 'retroperitoneal cystic lymphangioma']",,,,C2930929,,,,C535553,,,,
mondo:0021727,aberrant subclavian artery,"['aberrant right subclavian artery', 'aberrant left subclavian artery']",,,,C2936828,,,,C535555,,,,
mondo:0021736,proctosigmoiditis,"['Proctosigmoiditis', 'proctosigmoiditis', 'Rectosigmoiditis']",,,,C0033252,,C34950,,,569.89,,,
mondo:0021739,prurigo,"['Itchy skin eruption', 'Pruritic rash', 'Prurigo']",,,,C0033771,,,,D011536,698.8,,,
mondo:0021742,puerperal infection,"['Infection, Puerperal', 'Infections, Puerperal', 'Puerperal Infection', 'Puerperal Infections']",,,,C0034041,,,1001407,D011645,,,,
mondo:0021745,psychosocial short stature,"['abuse dwarfism syndrome', 'Kaspar Hauser syndrome', 'psychosocial dwarfism', 'child abuse dwarfism']",,,,C1455735,,,,C535569,,,,
mondo:0021746,pyelocystitis,"['Pyelocystitis', 'Cystopyelitis']",,,,C0034184,,,1001835,D053653,,,,
mondo:0021747,Acanthamoeba infectious disease,"['infections, Acanthamoeba', 'Acanthamoeba infection']",,,,,,,,,,,,
mondo:0021750,pyonephrosis,"['Hydronephrosis, Infected', 'pyonephrosis', 'Infected Hydronephrosis', 'Pyonephrosis']",,,,C0034216,,C123032,,D053018,,,,
mondo:0021752,Achard-Thiers syndrome,"['Achard Thiers syndrome', 'diabetic-bearded woman syndrome', 'diabetes in bearded women']",,,,C0271732,,,,C536013,,,,
mondo:0021758,acquired agranulocytosis,"['agranulocytic angina', 'granulocytopenia, primary', 'agranulocytosis, acquired', 'neutropenia, malignant']",,,,,,,,C538171,,,,
mondo:0021759,acquired fructose intolerance,"['dietary fructose intolerance', 'intestinal fructose intolerance', 'fructose malabsorption']",,,,,,,,,,,,
mondo:0021761,acral dysostosis dyserythropoiesis syndrome,,,,,,,,,,,,,
mondo:0021762,acrocoxomesomelic dysplasia,['acro-coxo-mesomelic dwarfism'],,,,,,,,,,,,
mondo:0021764,acrofacial dysostosis Preis type,,,,,,,,,,,,,
mondo:0021765,radiculitis,"['radiculitis', 'Nerve Root Inflammation', 'Radiculitides', 'Nerve Root Inflammations', 'Radiculitis', 'Inflammation, Nerve Root']",,,,C0034544,,C78581,,,729.2,,,
mondo:0021777,acute rheumatic heart disease,"['acute Rheumatic Heart Disease', 'acute rheumatic fever with heart involvement', 'acute rheumatic carditis', 'acute rheumatic heart disease', 'Active rheumatic fever with heart involvement']",,,,C0035440,,C34985,,,391.9,,,
mondo:0021783,streptococcal sore throat,"['Strep throat', 'Streptococcal angina', 'Strept throat', 'Streptococcal Pharyngitis', 'Streptococcal sore throat', 'Streptococcal pharyngitis', 'Septic sore throat', 'streptococcal pharyngitis', 'strep throat']",,,,C0036689,,C116003,1002024,,034.0,,,
mondo:0021804,silicotuberculosis,"['silicotuberculoses', 'silicotuberculosis']",,,,C0037118,,,,D012830,502,,,
mondo:0021805,"acromesomelic dysplasia, Campailla Martinelli type","['mesomelic dwarfism Campailla-Martinelli type', 'acromesomelic dysplasia Campailla Martinelli type']",,,,C2930969,,,,C535659,,,,
mondo:0021808,acute cholinergic dysautonomia,['ACD'],,,,C2930973,,,,C535672,,,,
mondo:0021809,primary dysautonomia,"['dysautonomia, primary', 'Dysautonomias', 'Dysautonomias, primary', 'dysautonomia', 'primary dysautonomia']",,,,,,,,D054969,,,,
mondo:0021811,acute mountain sickness,"['high altitude cerebral oedema', 'altitude sickness', 'high altitude pulmonary oedema', 'Mountain sickness', 'altitude anoxia', 'high altitude cerebral edema', 'high altitude pulmonary edema']",,,,C0238284,,,,,993.2,,,
mondo:0021812,adnexal spiradenoma/cylindroma of a sweat gland,"['cylindroma', 'adnexal sweat gland spiradenoma/cylindroma', 'cylindroma of skin', 'cylindroma of the skin', 'dermal cylindroma']",,,,,,C27094,,,,,,
mondo:0021824,"adult progressive spinal muscular atrophy, Aran Duchenne type","['Aran Duchenne spinal muscular atrophy', 'adult SMA Aran Duchenne type', 'adult progressive spinal muscular atrophy Aran Duchenne type']",,,,,,,,,,,,
mondo:0021826,aerobic Actinomyces infection,,,,,C2931717,,,,C538054,,,,
mondo:0021829,agnathia-microstomia-synotia,"['agnathia, microstomia, synotia and cardiac and pulmonary maldevelopment', 'Plurimalformative syndrome']",,,,C2931718,,,,C538059,,,,
mondo:0021834,Akaba Hayasaka syndrome,"['frontal bossing, cloudy corneae, low nasal ridge, and micrognathia, hypoplastic thorax, and rhizomelic micromelia']",,,,C2930948,,,,C535609,,,,
mondo:0021836,Aksu von Stockhausen syndrome,"['hereditary branchial arch defects', 'aksu von stockhausen syndrome']",,,,,,,,C535611,,,,
mondo:0021838,Al Gazali Khidr Prem Chandran syndrome,"['cherubism, optic atrophy and short stature']",,,,C2930951,,,,C535616,,,,
mondo:0021839,spirochaetales infections,"['Infection, Spirochete', 'Infection, Spirochaetales', 'INFECT SPIROCHETE', 'Infections, Spirochete', 'Infections, Spirochaetales', 'SPIROCHETE INFECT', 'Spirochetosis', 'Spirochete Infection', 'Spirochaetales Infections', 'Spirochete Infections', 'Spirochetal infection', 'INFECT SPIROCHAETALES', 'Spirochaetales Infection', 'SPIROCHAETALES INFECT']",,,,C0037974,,,,D013145,,,,
mondo:0021845,Aloi Tomasini Isaia syndrome,"['basal cell nevus, anodontia, abnormal bone mineralization', 'basal cell nevus anodontia abnormal bone mineralization', 'unilateral linear basal cell nevus associated with diffuse osteoma cutis, unilateral anodontia, and abnormal bone mineralization']",,,,C2931405,,,,C537049,,,,
mondo:0021851,alopecia universalis onychodystrophy vitiligo,"['alopecia universalis, onychodystrophy, and total vitiligo']",,,,C2931408,,,,C537056,,,,
mondo:0021856,Alsing syndrome,"['atypical macular coloboma, familial juvenile nephronophthisis and skeletal abnormality']",,,,C2931255,,,,C536588,,,,
mondo:0021879,small cell variant anaplastic large cell lymphoma,"['small cell variant anaplastic large cell lymphoma', 'anaplastic small cell lymphoma', 'small cell variant of anaplastic large cell lymphoma']",,,,C1335983,,C7208,,C538255,,,,
mondo:0021895,temporomandibular joint dysfunction syndrome,"['Myofascial pain - dysfunction syndrome of TMJ', 'TMJ syndrome', 'TMJ Syndrome', 'Temporomandibular Joint Dysfunction Syndrome', 'Temporomandibular Joint Syndrome', 'Syndrome, TMJ', 'Costen^s complex', 'Snapping jaw', 'Syndrome, Temporomandibular Joint', 'Temporomandibular joint syndrome', 'Costen Syndrome', 'TMJPDS - Temporomandibular joint pain dysfunction syndrome', 'Temporomandibular joint-pain-dysfunction syndrome', 'temporomandibular joint dysfunction syndrome', 'Costens Syndrome', 'Costen^s Syndrome', 'Myofascial Pain Dysfunction Syndrome, Temporomandibular Joint', 'Syndrome, Costen^s', 'Joint Syndrome, Temporomandibular', 'Temporomandibular joint pain dysfunction syndrome', 'Mandibular dysfunction', 'Costen^s syndrome']",,,,C0039496,,C35066,,D013706,,,,
mondo:0021896,anterior spinal artery stroke,,,,,C2931608,,,,C537776,,,,
mondo:0021902,aortopulmonary window,"['aortic-pulmonary window', 'APW', 'APSD', 'aortopulmonary septal defect', 'aorto-pulmonary window', 'AP window', 'aortopulmonary window']",,,,,,C101050,,D001028,,,,0011604
mondo:0021905,Apert-like polydactyly syndrome,['Apert like polydactyly syndrome'],,,,,,,,,,,,
mondo:0021907,aplasia cutis autosomal recessive,,,,,,,,,,,,,
mondo:0021908,aplasia cutis congenita dominant,,,,,,,,,,,,,
mondo:0021913,aquagenic pruritus,,,,,C0406409,,,,,698.8,,,
mondo:0021915,arakawa syndrome 2,"['Arakawa syndrome II', 'methionine synthase deficiency', 'tetrahydrofolate-methyltransferase deficiency syndrome', 'Arakawa^s syndrome II', 'N5-methylhomocysteine transferase deficiency', 'homocystinuria-megaloblastic Anemia, cblG complementation type', 'Arakawa^s syndrome 2', 'methylcobalamin deficiency, cblG type', 'tetrahydrofolate methyltransferase deficiency']",,,,C0268611,,C99081,,C537426,,,,
mondo:0021918,arena syndrome,['spastic paraplegia with iron deposits in basal ganglia'],,,,C2931491,,,,C537428,,,,
mondo:0021921,Arnold stickler bourne syndrome,"['corneal crystals myopathy and neuropathy', 'corneal crystals myopathy and nephropathy']",,,,C2931492,,,,C537431,,,,
mondo:0021923,Arroyo Garcia Cimadevilla syndrome,"['bilateral anophthalmia, esophageal atresia, and right cryptorchidism']",,,,C2931494,,,,C537439,,,,
mondo:0021925,tracheobronchitis,"['Tracheobronchitis', 'tracheobronchitis']",,,,C0040586,,C122784,,,,,,
mondo:0021927,arthrogryposis epileptic seizures migrational brain disorder,['arthrogryposis multiplex congenita with epileptic seizures and migrational brain disorder'],,,,C2931495,,,,C537442,,,,
mondo:0021929,traumatic myositis ossificans,"['Myositis ossificans circumscripta', 'traumatic myositis ossificans', 'Myositis ossificans traumatica', 'Traumatic myositis ossificans', 'Traumatic Myositis Ossificans']",,,,C0040798,,C35081,,,728.12,,,
mondo:0021932,infection by Trypanosoma gambiense,"['Gambian sleeping sickness', 'Infection by Trypanosoma gambiense', 'Gambiense trypanosomiasis infection', 'Gambian trypanosomiasis', 'chronic sleeping sickness', 'Infection caused by Trypanosoma gambiense']",,,,C0041232,,C35084,,,086.3,,,
mondo:0021935,aspergillus niger infection,"['Aspergillus niger infection', 'infections, Aspergillus niger', 'Aspergillus niger infection, pulmonary']",,,,,,,,C535390,,,,
mondo:0021941,infection by Trypanosoma rhodesiense,['rhodesian trypanosomiasis'],,,,C0041233,,C35085,,,086.4,,,
mondo:0021943,tuberculoma,"['Tuberculoma', 'Tuberculomas']",,,,C0041295,,,,D014375,,,,
mondo:0021944,auditory neuropathy,"['familial auditory neuropathy', 'auditory neuropathy spectrum disorder', 'progressive auditory neuropathy', 'ANSD', 'auditory dys-synchrony', 'auditory neuropathy']",,,,C2732267,,C116364,,C538268,,,,
mondo:0021945,hearing disorder,['hearing disorder'],,,,C0260662,,C3078,,D006311,,,,
mondo:0021948,cutaneous tuberculosis,"['Tuberculoderma', 'Skin Tuberculosis', 'Cutaneous tuberculosis', 'Cutaneous Tuberculosis', 'Cutaneous Tuberculoses', 'Tuberculosis cutis', 'Tuberculosis, Cutaneous', 'Tuberculosis of skin', 'Tuberculosis, Skin', 'Skin Tuberculoses', 'Tuberculoses, Skin', 'Tuberculoses, Cutaneous']",,,,C0041309,,,1001443,,,,,
mondo:0021950,autoimmune oophoritis,,,,,C0878654,,,,C538274,,,,
mondo:0021952,autoimmune progesterone dermatitis,['APD'],,,,C1260879,,,,C535299,708.8,,,
mondo:0021953,tuberculous fibrosis of lung,"['Tuberculous Fibrosis of Lung', 'tuberculous fibrosis of lung', 'Tuberculous fibrosis of lung']",,,,C0041336,,C35088,,,011.46,,,
mondo:0021957,autosomal recessive nonsyndromic congenital nuclear cataract,"['congenital nuclear cataract, autosomal recessive']",,,,C2931470,,,,C537298,,,,
mondo:0021960,ureteritis,"['ureteritis', 'Ureteritis', 'Inflammation of ureter']",,,,C0041959,,C78666,,,,,,
mondo:0021962,baetz-greenwalt syndrome,['hypoplastic right-sided heart complex'],,,,C2931615,,,,C537795,,,,
mondo:0021964,bagatelle Cassidy syndrome,"['macrocephaly, hypertelorism, short limbs, hearing loss, and developmental delay', 'macrocephaly short limbs deafness']",,,,C2931616,,,,C537796,,,,
mondo:0021966,baker Vinters syndrome,['hydrocephalus with cerebral aqueductal dysgenesis and craniofacial anomalies'],,,,C2931659,,,,C537899,,,,
mondo:0021969,Banti syndrome,"['Banti^s syndrome', 'idiopathic portal hypertension', 'idiopathic congestive splenomegaly', 'Banti^s disease']",,,,,,,,C537903,,,,
mondo:0021977,basaloid follicular hamartoma,,,,,C0474964,,C4749,,,706.1,,,
mondo:0021979,Basaran Yilmaz syndrome,"['keratoderma, hypotrichosis and leukonychia totalis']",,,,C2931577,,,,C537660,,,,
mondo:0021994,Berk-Tabatznik syndrome,"['kyphosis brachyphalangy optic atrophy', 'Berk Tabatznik syndrome', 'cleft nare, brachydactyly, short stature dwarfism', 'congenital optic atrophy and brachytelephalangy', 'short stature, congenital optic atrophy, and hypoplasia of the cervical vertebral bodies and distal phalanges', 'cleft nare, brachydactyly, short stature-dwarfism']",,,,C2930899,,,,C535432,,,,
mondo:0022007,water intoxication,"['Water intoxication syndrome', 'Water intoxication', 'WATER INTOX', 'Water Intoxication']",,,,C0043049,,,,D014869,,,,
mondo:0022011,bobble-head doll syndrome,"['BHDS', 'bobble head doll syndrome']",,,,,,,,C536241,,,,
mondo:0022013,Boerhaave syndrome,"['spontaneous rupture of the oesophagus', 'spontaneous rupture of oesophagus', 'spontaneous perforation of the esophagus', 'Boerhaave^s syndrome', 'spontaneous perforation of the oesophagus', 'spontaneous perforation of oesophagus', 'spontaneous rupture of the esophagus', 'Boerhave syndrome']",,,,C0238115,,,,C536571,,,,
mondo:0022020,Boudhina Yedes Khiari syndrome,,,,,C2931668,,,,C537939,,,,
mondo:0022022,bowenoid papulosis,"['Bowenoid papulosis', 'BP']",,,,C0334106,,C8374,,,447.8,,,
mondo:0022025,boylan dew greco syndrome,['congenital hypomyelination neuropathy with arthrogryposis multiplex congenita'],,,,C2931419,,,,C537083,,,,
mondo:0022034,lentivirus infection,"['Disease caused by Lentivirus', 'Lentivirus Infections', 'Infection, Lentivirus', 'Infections, Lentivirus', 'Lentivirus Infection', 'Disease due to Lentivirus']",,,,C0079680,,,1001357,D016180,,,,
mondo:0022037,large-cell immunoblastic lymphoma,"['Immunoblastic Large-Cell Lymphomas', 'Diffuse non-Hodgkin^s lymphoma, immunoblastic', 'Diffuse non-Hodgkin lymphoma, immunoblastic', 'LYMPHOMA IMMUNOBLASTIC LARGE', 'Sarcomas, Immunoblastic', 'Large-Cell Immunoblastic Lymphoma', 'Immunoblastic Lymphoma', 'Lymphoma, Large-Cell, Immunoblastic', 'Lymphosarcoma, Diffuse Immunoblastic', 'Lymphoma, Immunoblastic Large-Cell', 'Immunoblastic Sarcoma', 'Immunoblastic Sarcomas', 'Sarcoma, Immunoblastic', 'Lymphomas, Immunoblastic Large-Cell', 'Large-Cell Immunoblastic Lymphomas', 'Diffuse non-Hodgkin^s lymphoma, immunoblastic (clinical)', 'Lymphomas, Large-Cell Immunoblastic', 'Immunoblastic Lymphosarcoma, Diffuse', 'Diffuse Immunoblastic Lymphosarcoma', 'LARGE IMMUNOBLASTIC LYMPHOMA', 'Large cell immunoblastic lymphoma', 'Immunoblastic Large Cell Lymphoma', 'IMMUNOBLASTIC LARGE LYMPHOMA', 'Lymphosarcomas, Diffuse Immunoblastic', 'Immunoblastic Large-Cell Lymphoma', 'Immunoblastoma', 'Immunoblastomas', 'Lymphoma, immunoblastic, high grade', 'Large-Cell Lymphomas, Immunoblastic', 'Immunoblastic Lymphoma, Large-Cell', 'Lymphoma, Immunoblastic, Large-Cell', 'Malignant lymphoma - immunoblastic', 'Diffuse Immunoblastic Lymphosarcomas', 'Lymphoma, Large-Cell Immunoblastic', 'Lymphoma, Immunoblastic, Large Cell', 'Immunoblastic Lymphosarcomas, Diffuse', 'Large-Cell Lymphoma, Immunoblastic', 'Lymphoma, Large Cell, Immunoblastic', 'Immunoblastic Lymphomas, Large-Cell', 'Large Cell Immunoblastic Lymphoma', 'LYMPHOMA LARGE IMMUNOBLASTIC', 'Immunoblastic malignant lymphoma - large cell', 'Diffuse non-Hodgkin^s immunoblastic (diffuse) lymphoma']",,,,C0079746,,,,D016400,,,,
mondo:0022055,Calabro syndrome,"['craniosynostosis, limb abnormalities, brevicollis, micrognathia, pulmonary stenosis, and genital defects']",,,,C0796276,,,,C537960,,,,
mondo:0022057,calcifying epithelial odontogenic tumor,"['Pindborg tumor', 'Pindborg tumour', 'CEOT', 'calcifying epithelial odontogenic tumor']",,,,C0334574,,C54301,,C537961,,,,
mondo:0022060,calloso-genital dysplasia,['primary amenorrhoea with coloboma and total agenesis of the corpus callosum'],,,,C2931677,,,,C537962,,,,
mondo:0022067,Cantu sanchez-corona fragoso syndrome,"['severe mental deficiency proportionate dwarfism and delayed sexual maturation', 'severe mental deficiency, proportionate dwarfism, and delayed sexual maturation']",,,,C2930937,,,,C535571,,,,
mondo:0022070,Cantu sanchez-corona hernandez syndrome,,,,,,,,,,,,,
mondo:0022071,carbon baby syndrome,['universal acquired melanosis'],,,,C0406419,,,,,,,,
mondo:0022089,Carnevale hernandez castillo syndrome,['Triphalyngeal thumbs and brachyectrodactyly'],,,,C2930940,,,,C535585,,,,
mondo:0022094,Cartwright Nelson Fryns syndrome,"['Growth retardation, severe mental retardation, acral limb deficiencies with poorly keratinized nails', 'Growth retardation, severe intellectual disability, acral limb deficiencies with poorly keratinized nails']",,,,C2931062,,,,C535917,,,,
mondo:0022096,pyogenic granuloma,"['PG - Pyogenic granuloma', 'Capillary Hemangioma, Lobular', 'hemangiomatous Granulation Tissue', 'Lobular Hemangioma', 'Lobular Capillary Hemangioma', 'angiogranuloma', 'Granuloma telangiectaticum', 'Granuloma, Pyogenic', 'Granulation Tissue-Type Hemangioma', 'Granulomata Pyogenicum', 'Lobular capillary hemangioma', 'angiogranulomas', 'hemangioma, Lobular Capillary', 'Pyogenic Granuloma', 'Granuloma pyogenicum', 'Granuloma Pyogenicum', 'Granuloma Telangiecticum', 'Capillary hemangioma of granulation tissue type']",,,,C0085653,,,,D017789,,,,
mondo:0022098,catamenial pneumothorax,,,,,C0340007,,,,C538279,,,,
mondo:0022103,chronic prostatitis,"['chronic prostatitis', 'Chronic Prostatitis', 'Chronic prostatitis']",,,,C0085696,,C26930,,,601.1,,,
mondo:0022113,central centrifugal cicatricial alopecia,"['CENTRAL CENTRIFUGAL CICATRICIAL ALOPECIA', 'central centrifugal alopecia', 'CCCA']",,618352,,C1274708,,,,,704.09,,,
mondo:0022140,Charles bonnet syndrome,['CBS'],,,,C0339731,,,,D000075562,,,,
mondo:0022151,Chitty Hall Webb syndrome,"['bowed tibiae, radial anomalies, osteopenia, multiple fractures and developmental delay']",,,,C2931066,,,,C535929,,,,
mondo:0022171,chromhidrosis,['secretion of coloured sweat'],,,,,,,,,705.89,L75.1,,
mondo:0022173,chromosome 11q trisomy,"['partial duplication of chromosome 11q', 'trisomy 11q', 'Duplication 11q', 'partial trisomy 11q', 'partial trisomy of chromosome 11q', 'partial duplication of the long arm of chromosome type 11', '11q trisomy', 'chromosome 11q duplication', 'partial duplication of the long arm of chromosome 11', '11q duplication', 'partial trisomy of the long arm of chromosome 11']",,,262923,,,,,C538297,,,,
mondo:0022174,chromosome 12p deletion,"['partial monosomy 12p', 'partial monosomy of the short arm of chromosome 12', 'partial deletion of the short arm of chromosome type 12', '12p monosomy', '12p deletion', 'monosomy 12p', '12p-', 'loss of chromosome 12p', 'partial monosomy of chromosome 12p', '12p del', 'del(12p)', 'partial deletion of the short arm of chromosome 12', 'partial deletion of chromosome 12p', 'deletion 12p']",,,316244,C0795844,,C36410,,C538302,,,,
mondo:0022177,chromosome 13q trisomy,"['partial trisomy of the long arm of chromosome 13', 'partial duplication of the long arm of chromosome type 13', 'partial duplication of the long arm of chromosome 13', '13q trisomy', 'partial trisomy of chromosome 13q', 'Duplication 13q', 'chromosome 13q duplication', 'partial trisomy 13q', 'partial duplication of chromosome 13q', '13q duplication', 'trisomy 13q']",,,262932,C0795849,,,,C535485,,,,
mondo:0022178,chromosome 13q-mosaicism,['Mosiacism of chromosome 13q'],,,,CN037259,,,,C535486,,,,
mondo:0022180,chromosome 16 trisomy,"['trisomy chromosome 16', 'mosaic trisomy 16', 'trisomy 16']",,,,,,C37866,,,,,,
mondo:0022196,chronic erosive gastritis,"['varioliform gastritis', 'idiopathic chronic, erosive gastritis']",,,,C0267145,,,,,535.40,,,
mondo:0022202,disseminated,,,,,,,,,,,,,
mondo:0022205,pustular psoriasis,['Pustular psoriasis'],,,,C0152081,,,,,696.1,,,
mondo:0022208,crystal arthropathy,"['Crystal-induced arthritis AND/OR synovitis', 'Crystalline Arthropathy', 'Arthropathies, Crystalline', 'Crystal Arthropathies', 'Crystalline Arthritides', 'Crystal-related arthropathy and periarthropathy', 'Arthropathy, Crystal', 'Crystal Arthritides', 'Crystal Arthritis', 'Crystalline Arthritis', 'Arthritis, Crystalline', 'Arthropathies, Crystal', 'Crystalline arthritis', 'Arthritides, Crystalline', 'Arthritides, Crystal', 'Arthritis, Crystal', 'Crystalline Arthropathies', 'Crystal Arthropathy', 'Arthropathy, Crystalline', 'Crystal arthropathy']",,,,C0152087,,,,,712.98,,,
mondo:0022220,Parinaud syndrome,"['paralysis of vertical movement', 'Parinauds syndrome', 'vertical gaze palsy - Parinaud', 'dorsal midbrain syndrome', 'Parinaud^s syndrome', 'syndrome, Parinaud^s', 'Parinaud^s ophthalmoplegia', 'Parinaud syndrome', 'syndrome, Parinaud']",,,,C0152222,,C54102,,,,,,
mondo:0022236,colpocephaly,,,,,,,,,C535973,,,,
mondo:0022293,vascular disorder of penis,"['penile vascular disorder', 'Vascular disorder of penis', 'Penis vascular disorder', 'Penile vascular disorder', 'Penile Vascular Disorder']",,,,C0156307,,C35218,,,607.82,,,
mondo:0022308,corticobasal degeneration disorder,"['corticobasal syndrome', 'CBGD', 'cortico-basal ganglionic Degeneration (CBGD)', 'corticobasal degeneration', 'cortical-basal ganglionic degeneration', 'cortical basal ganglionic degeneration']",,,454887,,,C129069,,,,,,
mondo:0022311,cote katsantoni syndrome,['ectodermal dysplasia osteosclerosis'],,,,C2931195,,,,C536449,,,,
mondo:0022316,hair defect with photosensitivity and intellectual disability syndrome,"['kinky hair, photosensitivity, broken eyebrows and eyelashes, and nonprogressive mental retardation', 'hair defect with photosensitivity and intellectual disability', 'Calderon Gonzalez-Cantu syndrome', 'Calderón-González-Cantu syndrome', 'hair defect-photosensitivity-intellectual disability syndrome', 'kinky hair, photosensitivity, broken eyebrows and eyelashes, and nonprogressive intellectual disability', 'hair defect with photosensitivity and mental retardation']",,234030,1408,,,,,C537628,,,,
mondo:0022321,2-methylacetoacetyl CoA thiolase deficiency,,,,,C2930874,,,,C535307,,,,
mondo:0022323,2-hydroxyethyl methacrylate sensitization,"['2-HEMA sensitization', 'sensitization to 2-hydroxyethyl methacrylate']",,,,C2930873,,,,C535305,,,,
mondo:0022330,4-hydroxyphenylacetic aciduria,,,,,,,,,C535315,,,,
mondo:0022333,5-nucleotidase syndrome,"['5^NT syndrome', '5^-Nucleotidase syndrome']",,,,C2930876,,,,C535321,,,,
mondo:0022337,AIDS dysmorphic syndrome,,,,,,,,,,,,,
mondo:0022338,ALK+ histiocytosis,['anaplastic lymphoma kinase positive histiocytosis'],,,,,,,,,,,,
mondo:0022349,congenital absence of septum pellucidum,,,,,,,,,C535562,742.4,,,
mondo:0022357,congenital acardia,['congenital absence of the heart'],,,,,,,,,759.89,,,
mondo:0022380,acute lymphoblastic leukemia congenital sporadic aniridia,,,,,,,,,,,,,
mondo:0022394,cervical intraepithelial neoplasia,"['Intraepithelial Neoplasia of Cervix Uteri', 'Intraepithelial Neoplasia of the Uterine Cervix', 'Cervix Intraepithelial Neoplasia', 'Intraepithelial Neoplasia, Cervical', 'Intraepithelial Neoplasia of the Cervix Uteri', 'Cervical intraepithelial neoplasia', 'Cervical Intraepithelial Neoplasms', 'Uterine Cervix Intraepithelial Neoplasia', 'Cervical Dysplasia', 'Cervix Uteri Intraepithelial Neoplasia', 'Cervical Intraepithelial Neoplasm', 'Intraepithelial Neoplasms, Cervical', 'Neoplasia, Cervical Intraepithelial', 'Intraepithelial Neoplasia of Uterine Cervix', 'NEOPL CERVICAL INTRAEPITHELIAL', 'Intraepithelial Neoplasia of the Cervix', 'Neoplasm, Cervical Intraepithelial', 'Intraepithelial Neoplasm, Cervical', 'Neoplasms, Cervical Intraepithelial', 'Cervical Intraepithelial Neoplasia', 'Intraepithelial Neoplasia of Cervix']",,,,C0206708,,C3782,,,,,,
mondo:0022397,retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene,,,,156168,,,,,,,,,
mondo:0022398,aglossia and situs inversus,,,,,,,,,,,,,
mondo:0022399,retinal ciliopathy due to mutation in the RPGR gene,,,,156171,,,,,,,,,
mondo:0022400,retinal ciliopathy due to mutation in the RPGRIP gene,,,,156174,,,,,,,,,
mondo:0022401,agyria pachygyria polymicrogyria,,,,,,,,,,,,,
mondo:0022402,agyria-pachygyria type 1,"['Bielchowsky type of lissencephaly', 'type I lissencephaly']",,,,,,,,,,,,
mondo:0022403,Ahumada Del Castillo syndrome,"['Argonz Del Castillo syndrome', 'amenorrhea galactorrhea FSH decrease syndrome', 'nonpuerperal galactorrhe amenorrhea', 'galactorrhea amenorrhea without pregnancy', 'Argonz Ahumada Del Castillo syndrome']",,,,,,,,,,,,
mondo:0022404,retinal ciliopathy due to mutation in Usher gene,,,,156177,,,,,,,,,
mondo:0022405,retinal ciliopathy due to mutation in nephronophthisis gene,,,,156180,,,,,,,,,
mondo:0022407,retinal ciliopathy due to mutation in Bardet-Biedl gene,,,,156183,,,,,,,,,
mondo:0022409,nephropathy-associated ciliopathy,,,,156162,,,,,,,,,
mondo:0022410,retinal ciliopathy,,,,156165,,,,,,,,,
mondo:0022413,Albright-like syndrome,['Albright like syndrome'],,,,,,,,,,,,
mondo:0022414,allain-babin-demarquez syndrome,"['acro cephalo synostosis', 'craniosynostosis synostoses hypertensive nephropathy']",,,1526,,,,,,,,,
mondo:0022417,alopecia congenita keratosis palmoplantaris,"['alopecia congenita with hyperkeratosis of the palms and soles', 'alopecia congenita with keratosis palmoplantaris']",,,,,,,,C537050,,,,
mondo:0022424,alpha-mannosidosis type 1,,,,,C2931251,,,,C536584,,,,
mondo:0022425,alpha-thalassemia-abnormal morphogenesis,"['homozygous alpha-thalassemia, genital abnormalities, and terminal transverse limb defects', 'Abuelo Forman Rubin syndrome']",,,,,,,,,,,,
mondo:0022428,aluminosis,"['aluminum lung', 'aluminium lung']",,,,C0311227,,,,,,,,
mondo:0022430,persistent fetal circulation syndrome,"['persistent fetal circulation', 'PPHN', 'persistent pulmonary hypertension of the newborn', 'persistent foetal circulation']",,,,C0031190,,C85006,,D010547,,,,
mondo:0022432,alves Castelo dos Santos syndrome,"['ectodermal dysplasia syndrome of hypotrichosis, onychodysplasia, hyperkeratosis, kyphoscoliosis, and cataract']",,,,,,,,C536593,,,,
mondo:0022435,Mauriac syndrome,"['Mauriac syndrome', 'Mauriac^s syndrome', 'dwarfism-hepatomegaly-obesity-juvenile diabetes syndrome']",,,,C0221005,,C130997,,,258.1,,,
mondo:0022444,amyloidosis bronchopulmonary,,,,,,,,,,,,,
mondo:0022453,angiomyomatous hamartoma,,,,,C2959445,,,,,,,,
mondo:0022454,angiosarcoma of the scalp,['scalp angiosarcoma (disease)'],,,,,,,,,,,,
mondo:0022456,ankle defects short stature,,,,,,,,,,,,,
mondo:0022457,ankyloblepharon filiforme imperforate anus,,,,1074,,,,,,,,,
mondo:0022458,annular constricting bands,,,,,,,,,,,,,
mondo:0022461,anophthalmia cleft palate micrognathia,,,,,,,,,,,,,
mondo:0022462,anophthalmia esophageal atresia cryptorchidism,,,,,,,,,,,,,
mondo:0022465,anotia facial palsy cardiac defect,,,,,,,,,,,,,
mondo:0022468,antigen-peptide-transporter 2 deficiency,"['antigen processing (TAP) deficiency syndrome', 'TAP 2 deficiency']",,,,,,,,,,,,
mondo:0022470,aortic dissection lentiginosis,,,,,,,,,,,,,
mondo:0022471,childhood aortic valve stenosis,['aortic valves stenosis of the child'],,,,,,,,,,,,
mondo:0022481,APO A-i deficiency,,,,,,,,,,,,,
mondo:0022496,arthrogryposis IUGR thoracic dystrophy,['Van Bervliet syndrome'],,,,,,,,,,,,
mondo:0022500,arthrogryposis multiplex congenita CNS calcification,,,,,,,,,,,,,
mondo:0022504,arthrogryposis spinal muscular atrophy,,,,,,,,,,,,,
mondo:0022509,asternia,['absent sternum'],,,,,,,,,,,,
mondo:0022510,atlanto-axial fusion,"['atlantoaxial fusion', 'atlantoaxial joint fusion']",,,,,,,,C538196,,,,
mondo:0022513,atrophoderma of Pierini and Pasini,"['congenital atrophoderma of Pasini and Pierini', 'idiopathic atrophoderma of Pasini and Pierini']",,,,,,,,,,L90.3,,
mondo:0022518,autoimmune inner ear disease,['AIED'],,,,,,,,,,,,
mondo:0022519,autoimmune myocarditis,,0080767,,,,,,,,,,,
mondo:0022529,BK-virus nephropathy,"['Polyomavirus nephropathy', 'PVAN', 'BKN', 'BK virus nephropathy', 'polyomavirus associated nephropathy', 'nephropathy from BK virus']",0040086,,,C1697878,,,,,079.89,,,
mondo:0022535,autonomic facial cephalgia,"['Carotidynia', 'Carotodynia', 'Autonomic facial cephalgia']",,,,C0238902,,,,,337.09,,,
mondo:0022538,leukoplakia of gingiva,"['gingival leukoplakia', 'Gingival Leukoplakia', 'leukoplakia of gingiva', 'Leukoplakia of gingiva', 'Leukoplakia of Gingiva']",,,,C0239737,,C3881,,,528.6,,,
mondo:0022545,Barnicoat Baraitser syndrome,"['polysyndactyly overgrowth syndrome', 'Barnicoat-Baraitser syndrome']",,,,,,,,,,,,
mondo:0022551,Basedow^s coma,"['Coma basedovicum', 'Karl Adolph von Basedow']",,,,,,,,,,,,
mondo:0022552,Bazopoulou Kyrkanidou syndrome,,,,,C2931580,,,,C537664,,,,
mondo:0022553,BD syndrome,,,,,,,,,,,,,
mondo:0022555,Beardwell syndrome,['familial ankylosing vertebral hyperostosis with tylosis'],,,,C2931581,,,,C537665,,,,
mondo:0022557,Behrens Baumann dust syndrome,"['microphthalmia-optic nerve dysplasia', 'unilateral aplasia of the optic nerve with cryptophthalmus and contralateral microphthalmus', 'Behrens-Baumann-Vogel syndrome', 'oculo-cerebral dysplasia']",,,,,,,,C537670,,,,
mondo:0022559,benign angiitis of the central nervous system,['BACNS'],,,,,,,,,,,,
mondo:0022560,benign metastasizing leiomyoma,,,,,,,,,,,,,
mondo:0022567,bhaskar jagannathan syndrome,,,,,C2930901,,,,C535437,,,,
mondo:0022568,bidirectional tachycardia,['bidirectional ventricular tachycardia'],,,,C2930902,,,,C535438,,,,
mondo:0022572,bilateral renal agenesis dominant type,,,,,,,,,,,,,
mondo:0022573,biliary atresia intrahepatic non syndromic form,,,,,,,,,,,,,
mondo:0022574,biliary atresia intrahepatic syndromic form,,,,,,,,,,,,,
mondo:0022575,biliary hypoplasia,,,,,,,,,,,,,
mondo:0022576,bilirubin induced brain injury in the newborn,,,,,,,,,,,,,
mondo:0022577,Billet bear syndrome,['Lower limb partial duplication renal agenesis'],,,,,,,,,,,,
mondo:0022578,childhood bladder carcinoma,"['bladder cancer', 'bladder cancer childhood', 'bladder carcinoma, childhood', 'childhood bladder carcinoma', 'childhood bladder cancer', 'bladder cancer, childhood']",,,,C3899675,,C118816,,,,,,
mondo:0022580,blepharo naso facial syndrome van Maldergem type,,,,,,,,,,,,,
mondo:0022586,bone dysplasia Moore type,,,,,,,,,,,,,
mondo:0022587,bone dysplasia corpus callosum agenesis,,,,,,,,,,,,,
mondo:0022598,brachydactyly absence of distal phalanges,,,,,,,,,,,,,
mondo:0022599,brachydactyly anonychia,,,,,,,,,,,,,
mondo:0022602,brachydactyly small stature face anomalies,,,,,,,,,,,,,
mondo:0022603,brachydactyly tibial hypoplasia,,,,,,,,,,,,,
mondo:0022606,branchial arch disease,"['disorder of pharyngeal system development', 'disease of pharyngeal system development', 'pharyngeal system development disease']",,,,,,,,,,,,
mondo:0022607,extraovarian Brenner tumor of the vagina,"['Brenner tumour of the vagina', 'vagina Brenner tumor', 'Brenner tumor of the vagina', 'vagina Brenner tumour', 'extraovarian Brenner tumor of the vagina']",,,,,,,,,,,,
mondo:0022608,brittle bone syndrome lethal type,,,,,,,,,,,,,
mondo:0022609,bronchial adenomas/carcinoids childhood,['bronchial carcinoids'],,,,C4013426,,,,,,,,
mondo:0022610,bronchiectasis oligospermia,,,,,,,,,,,,,
mondo:0022611,Brunoni syndrome,"['mesomelia, radial hypoplasia bifid thumb unusual facies', 'mesomelic dwarfism, skeletal abnormalities, and ectodermal dysplasia']",,,,C2931486,,,,C537408,,,,
mondo:0022612,Brunsting-Perry syndrome,"['localised cicatricial pemphigoid', 'cicatricial pemphigoid of the Brunsting-Perry type', 'Brunsting Perry syndrome', 'localized cicatricial pemphigoid']",,,,C1304226,,,0008611,,,,,
mondo:0022613,bruyn scheltens syndrome,,,,,,,,,,,,,
mondo:0022615,burn goodship syndrome,,,,,,,,,,,,,
mondo:0022618,burning mouth syndrome type 3,"['BMS-3', 'type 3 burning mouth syndrome', 'Psychiatric disorders coexisting with burning mouth syndrome']",,,,C2931487,,,,C537413,,,,
mondo:0022622,congenital disorder of glycosylation syndrome type 4,['CDG syndrome type 4'],,,,,,,,,,,,
mondo:0022623,CDK4 linked melanoma,,,,,,,,,,,,,
mondo:0022633,camptodactyly joint contractures and facial skeletal dysplasia,,,,,,,,,C537969,,,,
mondo:0022634,camptodactyly vertebral fusion,"['camptodactyly and sacral vertebral fusion (subtype)', 'camptodactyly and sacral vertebral fusion']",,,,C2931682,,,,C537973,,,,
mondo:0022636,candida glabrata infection,"['Torulopsis glabrata (formerly)', 'candida glabrata']",,,,,,,,,,,,
mondo:0022639,Cantu sanchez-corona Garcia-Cruz syndrome,,,,,,,,,,,,,
mondo:0022642,childhood carcinoid tumor,"['carcinoid tumour childhood', 'carcinoid tumour (disease) of childhood', 'carcinoid tumor childhood', 'paediatric carcinoid tumour (disease)', 'childhood carcinoid tumour (disease)', 'pediatric carcinoid tumor (disease)', 'childhood carcinoid tumor', 'carcinoid tumor (disease) of childhood']",,,,C3899673,,C118810,,,,,,
mondo:0022643,carcinoma of the vocal tract,"['carcinoma of laryngeal vocal fold', 'laryngeal vocal fold carcinoma']",,,,,,,,,,,,
mondo:0022644,cardiac hydatid cysts with intracavitary expansion,['Cardiac hydatidosis'],,,,,,,,,,,,
mondo:0022645,cardioencephalomyopathy,,,,,,,,,,,,,
mondo:0022646,cardiofacial syndrome short limbs,,,,,,,,,,,,,
mondo:0022647,cardiomelic syndrome stratton Koehler type,,,,,,,,,,,,,
mondo:0022648,cardiomyopathy and deafness due to tRNA lysine gene mutation,"['cardiomyopathy and deafness due to tRNA lysine gene mutation', 'cardiomyopathy and deafness due to MTTK gene mutation']",,,,CN036924,,,,,,,,
mondo:0022650,cardiomyopathy diabetes deafness,,,,,,,,,,,,,
mondo:0022653,cardiomyopathy due to anthracyclines,,,,,,,,,,,,,
mondo:0022654,cardiomyopathy hypogonadism collagenoma syndrome,['cardiomyopathy-hypogonadism-collagenoma syndrome'],,,,,,,,C535582,,,,
mondo:0022655,cardiomyopathy hypogonadism metabolic anomalies,,,,,C2931289,,,,,,,,
mondo:0022656,cardiomyopathy spherocytosis,,,,,,,,,,,,,
mondo:0022662,carpo tarsal osteolysis recessive,,,,,,,,,,,,,
mondo:0022666,cassavism,,,,,,,,,,,,,
mondo:0022672,autosomal dominant cataract,['cataract congenital autosomal dominant'],,,,,,,,,,,,
mondo:0022673,autosomal dominant non-nuclear cataract,"['PCC', 'cataract, polymorphic congenital', 'cataract, Nonnuclear polymorphic congenital, autosomal dominant', 'autosomal dominant nonnuclear polymorphic congenital cataract', 'CCP', 'cataract congenital dominant non nuclear']",,601286,,,,,,C538284,,,,
mondo:0022675,cataract skeletal anomalies,,,,,,,,,,,,,
mondo:0022682,cennamo gangemi syndrome,['hydrocephalus cataract microphthalmos'],,,,,,,,,,,,
mondo:0022685,cerebellar agenesis,,,,,,,,,,,,,
mondo:0022687,cerebellar degeneration,"['neurodegenerative disease of cerebellum', 'cerebral degeneration', 'cerebellum neurodegenerative disease', 'cerebellar Degeneration', 'Brain degeneration']",1443,,,C0262404,,C84624,,,331.9,,,
mondo:0022691,cerebello-olivary atrophy,['Cerebelloolivary atrophy'],,,,,,,,,,,,
mondo:0022693,cerebral calcification cerebellar hypoplasia,,,,,,,,,,,,,
mondo:0022694,cerebral calcifications opalescent teeth phosphaturia,,,,,,,,,,,,,
mondo:0022697,athetoid cerebral palsy,"['cerebral palsy dyskinetic', 'dyskinetic cerebral palsy', 'athetoid dyskinetic cerebral palsy', 'athetoid cerebral palsy', 'ADCP']",0050672,,,C0270742,,C97169,,,,G80.3,,
mondo:0022699,cerebral palsy spastic hemiplegic,"['spastic hemiplegic cerebral palsy', 'spastic hemiplegia cerebral palsy']",,,,,,,,,,,,
mondo:0022700,cerebral palsy spastic monoplegic,"['spastic monoplegia cerebral palsy', 'spastic monoplegic cerebral palsy']",,,,,,,,,,,,
mondo:0022712,oculo digital syndrome,"['Chemke Oliver Mallek syndrome', 'Chemke-Oliver-Mallek syndrome', 'multiple ophthalmic anomalies and digital hypoplasia']",,,,C2931063,,,,C535922,,,,
mondo:0022714,chester porphyria,"['PORC', 'porphyria, Chester type']",,176010,,,,,,,,,,
mondo:0022715,Chiari malformation type 3,"['Chiari malformation type III', 'Arnold Chiari malformation type III', 'Chiari type III malformation']",,,,,,,,,,,,
mondo:0022716,Chiari malformation type 4,"['Arnold Chiari malformation type IV', 'Chiari malformation type IV', 'Chiari type IV malformation']",,,,,,,,,,,,
mondo:0022723,chondrodysplasia,,,,,,,,,,,,,
mondo:0022729,chondrodysplasia punctata with steroid sulfatase deficiency,,,,,,,,,,,,,
mondo:0022733,choreoacanthocytosis amyotrophic,,,,,,,,,,,,,
mondo:0022734,chorioretinopathy dominant form microcephaly,,,,,,,,,,,,,
mondo:0022735,choroid plexus cyst,,,,,,,C4351,,,,,,
mondo:0022736,occupational lung disease,"['Occupational inhalation disease', 'Occupational pulmonary disease', 'Occupational respiratory disease', 'Occupational lung disorder', 'Occupational lung disease']",,,,C0264421,,,,,508.9,,,
mondo:0022737,choroideremia hypopituitarism,,,,,C4275146,,,,,,,,
mondo:0022739,Christian demyer franken syndrome,,,,,,,,,,,,,
mondo:0022740,Christian Johnson angenieta syndrome,,,,,,,,,,,,,
mondo:0022742,occupational asthma,"['Industrial asthma', 'Occupational Asthmas', 'Occupational Asthma', 'Asthma, Occupational', 'Asthmas, Occupational', 'Occupational asthma']",0080820,,,C0264423,,,,D059366,,,,
mondo:0022745,mixed dust pneumoconiosis,"['labrador lung', 'Mixed dust pneumoconiosis']",,,,C0264436,,,,,504,,,
mondo:0022746,chromosome 13p duplication,"['chromosome 13p, trisomy', 'trisomy 13p', 'Duplication 13p']",,,,CN037021,,,,C535450,,,,
mondo:0022749,non-neoplastic nevus,"['non-neoplastic nevus', 'Non-Neoplastic Nevus', 'Non-neoplastic nevus']",,,,C0265027,,C3937,,,448.1,,,
mondo:0022752,chromosome 16p13.3 deletion syndrome,"['RSTS, Severe', 'Rubinstein-Taybi syndrome, Severe']",,,,C3502510,,,,C566433,,,,
mondo:0022754,chromosome 17p deletion,"['chromosome 17p deletion syndrome', 'partial deletion of the short arm of chromosome 17', 'del(17p)', 'loss of chromosome 17p', 'monosomy 17p', 'deletion 17p', 'partial monosomy of the short arm of chromosome type 17', 'partial monosomy 17p', '17p- syndrome', 'deletion 17p syndrome', 'partial deletion of chromosome 17p', 'chromosome 17p deletion', '17p deletion', 'partial monosomy of the short arm of chromosome 17', 'partial monosomy of chromosome 17p', 'interstitial deletion 17p', '17p monosomy']",,,261965,CN036220,,C36499,,C538045,,,,
mondo:0022755,chromosome 18 mosaic monosomy,"['monosomy 18 mosaicism', 'Mosaic monosomy chromosome 18', 'Mosaic monosomy 18']",,,,CN036727,,,,C536581,,,,
mondo:0022756,chromosome 1q deletion,"['partial monosomy of chromosome 1q', 'partial deletion of the long arm of chromosome type 1', 'deletion 1q', '1q deletion', 'monosomy 1q', 'partial monosomy of the long arm of chromosome 1', 'partial monosomy 1q', '1q monosomy', 'partial deletion of the long arm of chromosome 1', 'partial deletion of chromosome 1q']",,,262001,CN072190,,,,,,,,
mondo:0022757,chromosome 20 trisomy,"['trisomy 20', 'trisomy 20 mosaicism', 'trisomy chromosome 20', 'mosaic trisomy 20']",,,,C0265479,,C36397,,C535372,,,,
mondo:0022758,"chromosome 22, monosome mosaic","['Mosaic monosome 22', 'chromosome 22 mosaic monosomy']",,,,CN036765,,,,C536798,,,,
mondo:0022759,trisomy 22,['chromosome 22 trisomy'],,,,C0265490,,,,C536799,,,,
mondo:0022760,chromosome 22q deletion,"['partial deletion of chromosome 22q', 'partial deletion of the long arm of chromosome type 22', '22q monosomy', 'partial monosomy of the long arm of chromosome 22', '22q deletion', 'monosomy 22q', 'partial deletion of the long arm of chromosome 22', 'partial monosomy 22q', 'partial monosomy of chromosome 22q', 'deletion 22q']",,,262182,,,,,,,,,
mondo:0022761,chromosome 3 duplication syndrome,,,,,C2931333,,,,C536803,,,,
mondo:0022762,chromosome 4 short arm deletion,"['4p deletion', 'partial deletion of the short arm of chromosome type 4', 'partial monosomy of chromosome 4p', 'partial monosomy 4p', 'partial monosomy of the short arm of chromosome 4', 'monosomy 4p', 'chromosome 4p deletion', '4p monosomy', 'partial deletion of the short arm of chromosome 4', 'partial deletion of chromosome 4p', 'deletion 4p']",,,261884,,,,,C537637,,Q93.3,,
mondo:0022765,chronic demyelinizing neuropathy with IgM monoclonal,,,,,,,,,,,,,
mondo:0022768,chronic polyradiculoneuritis,,,,,,,,,,,,,
mondo:0022769,ciliary dyskinesia-bronchiectasis,,,,,,,,,,,,,
mondo:0022770,circumscribed cutaneous aplasia of the vertex,,,,,,,,,,,,,
mondo:0022771,circumscribed disseminated keratosis Jadassohn lew type,,,,,,,,,,,,,
mondo:0022772,classic Kaposi sarcoma,"['Kaposi sarcoma classical type', 'classic Kaposi sarcoma', 'Kaposi sarcoma, classic', 'Kaposi^s sarcoma, classical type', 'classic Kaposi^s sarcoma']",,,,C0279084,,C9112,,,,,,
mondo:0022775,cleft lip and palate malrotation cardiopathy,,,,,,,,,,,,,
mondo:0022776,cleft lip and/or palate with mucous cysts of lower,,,,,,,,,,,,,
mondo:0022777,cleft lip palate dysmorphism kumar type,,,,,,,,,,,,,
mondo:0022778,cleft lip palate intellectual disability corneal opacity,,,,,,,,,,,,,
mondo:0022779,cleft lip palate oligodontia syndactyly pili torti,,,,,,,,,,,,,
mondo:0022780,cleft lip palate pituitary deficiency,,,,,,,,,,,,,
mondo:0022781,cleft lip palate-tetraphocomelia,,,,,,,,,,,,,
mondo:0022782,cleft lower lip cleft lateral canthi chorioretinal,,,,,,,,,,,,,
mondo:0022785,cleft palate cardiac defect ectrodactyly,,,,,,,,,,,,,
mondo:0022786,cleft palate colobomata radial synostosis deafness,,,,,,,,,,,,,
mondo:0022787,cleft palate heart disease polydactyly absent tibia,,,,,,,,,,,,,
mondo:0022790,cleft tongue,"['bifid tongue', 'cleft tongue syndrome']",,,,,,,,,,,,
mondo:0022791,coarse face hypotonia constipation,['Sondheimer syndrome'],,,,,,,,,,,,
mondo:0022792,coccygodynia,['coccydynia'],,,,,,,,,,,,
mondo:0022795,deficiency of coenzyme q cytochrome c reductase,['coenzyme Q cytochrome c reductase deficiency of'],,,,,,,,,,,,
mondo:0022798,Cohen lockood wyborney syndrome,,,,,,,,,,,,,
mondo:0022799,cold urticaria,"['urticaria idiopathic cold', 'primary idiopathic cold urticaria', 'cold contact urticaria']",,,,C0221207,,,1001881,,,,,
mondo:0022800,type 2 collagenopathy,"['disease or disorder caused by mutation in COL2A1', 'collagenopathy type 2 alpha 1', 'collagen II', 'cartilage collagen', 'COL2A1 disease or disorder', 'COL2A1']",,,93421,CN227672,,,,C535964,,,,
mondo:0022802,Collins-Sakati syndrome,['Collins Sakati syndrome'],,,,,,,,,,,,
mondo:0022803,coloboma porencephaly hydronephrosis,,,,,,,,,,,,,
mondo:0022804,colobomata unilobar lung heart defect,,,,,,,,,,,,,
mondo:0022805,colonic malakoplakia,,,,,,,,,,,,,
mondo:0022809,Colver Steer Godman syndrome,,,,,,,,,,,,,
mondo:0022810,Combarros Calleja Leno syndrome,,,,,,,,,,,,,
mondo:0022812,complement receptor deficiency,,,,,C0398783,,,,,279.8,,,
mondo:0022815,congenital absence of the sternocleidomastoid muscle,,,,,C2931075,,,,C535977,,,,
mondo:0022817,congenital amputation,,,,,,,,,,,,,
mondo:0022818,congenital aneurysms of the great vessels,,,,,,,,,,,,,
mondo:0022819,congenital arteriovenous shunt,,,,,,,,,,,,,
mondo:0022820,congenital articular rigidity,,,,,,,,,,,,,
mondo:0022821,congenital benign spinal muscular atrophy dominant,,,,,,,,,,,,,
mondo:0022822,congenital cardiovascular shunt,,,,,,,,,,,,,
mondo:0022823,congenital contractures,,,,,,,,,,,,,
mondo:0022824,congenital craniosynostosis maternal hyperthyroiditis,,,,,,,,,,,,,
mondo:0022825,congenital cystic eye,['CCE'],,,519384,,,,,,,,,
mondo:0022826,congenital cystic eye multiple ocular and intracranial anomalies,,,,,,,,,,,,,
mondo:0022831,congenital heart disease ptosis hypodontia craniostosis,,,,,,,,,,,,,
mondo:0022832,congenital heart disease radio ulnar synostosis intellectual disability,,,,,,,,,,,,,
mondo:0022839,congenital human immunodeficiency virus,"['congenital HIV', 'neonatal HIV', 'neonatal human immunodeficiency virus']",,,,C0520783,,,,,,,,
mondo:0022841,congenital hypotrichosis milia,,,,,,,,,,,,,
mondo:0022843,congenital mumps,,,,,,,,,,,,,
mondo:0022846,congenital nonhemolytic jaundice,,,,,,,,,,,,,
mondo:0022849,congenital stenosis of cervical medullary canal,,,,,,,,,,,,,
mondo:0022851,Dennis-Fairhurst-Moore syndrome,"['Hallermam Streiff like syndrome', 'Dennis Fairhurst Moore syndrome']",,,2109,,,,,C538210,,,,
mondo:0022854,congenital unilateral pulmonary hypoplasia,,,,,,,,,,,,,
mondo:0022855,congenital vagal hyperreflexivity,,,,,,,,,,,,,
mondo:0022858,continuous spike-wave during slow sleep syndrome,,,,,,,,,,,,,
mondo:0022859,cor biloculare,"['TWO-chambered heart', 'Cor Biloculare']",,,,C0152238,,C124591,,,745.7,,,
mondo:0022862,cormier rustin munnich syndrome,,,,,,,,,,,,,
mondo:0022863,corneal crystals myopathy neuropathy,,,,,,,,,,,,,
mondo:0022865,corneal dystrophy ichthyosis microcephaly intellectual disability,,,,,,,,,,,,,
mondo:0022866,corneal dystrophy pigmentary anomaly malabsorption,,,,,,,,,,,,,
mondo:0022869,coronary arteries congenital malformation,,,,,,,,,,,,,
mondo:0022871,corpus callosum agenesis of blepharophimosis robin type,,,,,,,,,,,,,
mondo:0022872,corpus callosum dysgenesis X-linked recessive,,,,,,,,,,,,,
mondo:0022873,corpus callosum dysgenesis cleft spasm,,,,,,,,,,,,,
mondo:0022874,corpus callosum dysgenesis hypopituitarism,,,,,,,,,,,,,
mondo:0022875,cortada Koussef Matsumoto syndrome,,,,,,,,,,,,,
mondo:0022876,Cortes Lacassie syndrome,,,,,,,,,,,,,
mondo:0022883,craniofacial and skeletal defects,,,,,,,,,,,,,
mondo:0022884,craniofacial dysostosis arthrogryposis progeroid appearence,['Van Biervliet Hendrickx Van Ertbruggen syndrome'],,,,,,,,,,,,
mondo:0022887,craniofrontonasal syndrome Teebi type,,,,,,,,,,,,,
mondo:0022888,craniostenosis cataract,,,,,,,,,,,,,
mondo:0022889,craniostenosis with congenital heart disease intellectual disability,,,,,,,,,,,,,
mondo:0022890,craniosynostosis Fontaine type,,,,,,,,,,,,,
mondo:0022891,craniosynostosis Maroteaux Fonfria type,,,,,,,,,,,,,
mondo:0022892,craniosynostosis alopecia brain defect,,,,,,,,,,,,,
mondo:0022893,craniosynostosis arthrogryposis cleft palate,,,,,,,,,,,,,
mondo:0022894,craniosynostosis autosomal dominant,,,,,,,,,,,,,
mondo:0022895,craniosynostosis cleft lip palate arthrogryposis,,,,,,,,,,,,,
mondo:0022896,craniosynostosis contractures cleft,,,,,,,,,,,,,
mondo:0022897,craniosynostosis exostoses nevus epibulbar dermoid,,,,,,,,,,,,,
mondo:0022898,craniosynostosis intellectual disability heart defects,,,,,,,,,,,,,
mondo:0022899,crawfurd syndrome,,,,,,,,,,,,,
mondo:0022900,athyreotic congenital hypothyroidism,['cretinism athyreotic'],,,,,,,,,,,,
mondo:0022901,Crohn disease of the esophagus,"['Crohn^s disease of the esophagus', 'Crohn^s disease of the oesophagus']",,,,C0341116,,,,,,,,
mondo:0022904,cryofibrinogenemia,,,,,C0272263,,,,C536218,286.9,,,
mondo:0022907,cutaneous sclerosis,,,,,,,,,,,,,
mondo:0022908,cutis gyratum acanthosis nigricans craniosynostosis,,,,,,,,,,,,,
mondo:0022909,cutis laxa osteoporosis,,,,,,,,,,,,,
mondo:0022912,cutis verticis gyrata mental deficiency,,,,,C1857444,,,,,,,,
mondo:0022913,cutler bass Romshe syndrome,,,,,,,,,,,,,
mondo:0022919,cytokine receptor deficiency,"['cytokine receptor activity disease', 'disorder of cytokine receptor activity']",,,,,,,,,,,,
mondo:0022930,Dandy-Walker malformation with nasopharyngeal teratoma and diaphragmatic hernia,['Aughton sloan Milad syndrome'],,,,C2931823,,,,C538340,,,,
mondo:0022932,Davenport-Donlan syndrome,"['dominant hearing loss, white hair, contractures, hyperkeratotic papillomata, and depressed chemotaxis', 'Davenport Donlan syndrome']",,,3215,C2931076,,,,C535988,,,,
mondo:0022934,Davis Lafer syndrome,"['mental retardation unusual facies Davis Lafer type', 'intellectual disability unusual facies Davis Lafer type', 'Lafer Davis syndrome']",,,,C2931077,,,,C535989,,,,
mondo:0022936,de Hauwere Leroy adriaenssens syndrome,"['iris dysplasia, orbital hypertelorism, and psychomotor retardation']",,,,C2931078,,,,C535991,,,,
mondo:0022937,deafness conductive stapedial ear malformation facial palsy,,,,,,,,,,,,,
mondo:0022938,deafness goiter stippled epiphyses,,,,,,,,,,,,,
mondo:0022941,deafness hypospadias metacarpal and metatarsal syndrome,,,,,,,,,,,,,
mondo:0022942,deafness mesenteric diverticula of small bowel neuropathy,,,,,,,,,,,,,
mondo:0022945,deafness peripheral neuropathy arterial disease,,,,,,,,,,,,,
mondo:0022946,deafness progressive cataract autosomal dominant,,,,,,,,,,,,,
mondo:0022948,Deal Barratt Dillon syndrome,"['Fanconi syndrome, ichthyosis, dysmorphism, jaundice and diarrhea', 'Fanconi syndrome, ichthyosis, dysmorphism, jaundice and diarrhoea']",,,,C2931773,,,,C538206,,,,
mondo:0022949,defective apolipoprotein b-100,,,,,,,,,,,,,
mondo:0022953,delta-1-pyrroline-5-carboxylate dehydrogenase deficiency,"['1-pyrroline-5-carboxylate dehydrogenase activity disease', 'disorder of 1-pyrroline-5-carboxylate dehydrogenase activity']",,,,,,,,,,,,
mondo:0022960,dermatocardioskeletal syndrome boronne type,,,,,,,,,,,,,
mondo:0022963,desmoplastic infantile astrocytoma,"['Desmoplastic infantile astrocytoma', 'Desmoplastic astrocytoma of infancy', 'DIA']",,,,C0457179,,C9476,,,,,,
mondo:0022965,desmoplastic infantile ganglioglioma,"['DIG', 'Desmoplastic infantile ganglioglioma']",0081259,,,C1321878,,C4738,,,,,,
mondo:0022968,dextrocardia with situs inversus,['situs inversus totalis'],,,,,,,,,,,,
mondo:0022971,diabetes persistent mullerian ducts,,,,,,,,,,,,,
mondo:0022972,diabetic mastopathy,"['diabetic fibrous breast disease', 'diabetic fibrous mastopathy', 'sclerosing lymphocytic lobulitis', 'lymphocytic mastitis', 'lymphocytic mastopathy']",,,,,,,,C537524,,,,
mondo:0022975,diaphragmatic agenesis radial aplasia omphalocele,,,,,,,,,,,,,
mondo:0022977,diaphragmatic hernia exomphalos corpus callosum agenesis,,,,,,,,,,,,,
mondo:0022978,diaphragmatic hernia upper limb defects,,,,,,,,,,,,,
mondo:0022981,die Smulders droog van dijk syndrome,,,,,,,,,,,,,
mondo:0022982,die Smulders Vles Fryns syndrome,,,,,,,,,,,,,
mondo:0022983,Dieterich disease,"['avascular necrosis of the metacarpal head', 'Dieterich disease', 'Dieterich^s disease']",,,,C2931124,,,,C536172,,,,
mondo:0022985,diffuse cavernous hemangioma of the rectum,['cavernous haemangioma of the rectum'],,,,,,,,,,,,
mondo:0022986,diffuse idiopathic pulmonary neuroendocrine cell hyperplasia,"['diffuse idiopathic pulmonary neuroendocrine cell hyperplasia', 'DIPNECH', 'DIP-NECH']",,,617916,C1333291,,C7437,,,,,,
mondo:0022989,diomedi bernardi placidi syndrome,,,,,,,,,,,,,
mondo:0022990,diphallus rachischisis imperforate anus,,,,,,,,,,,,,
mondo:0022991,diploid-triploid mosaicism,"['diploid/triploid mixoploidy', 'diploid/triploid mosaicism', 'Mosaic triploidy', 'Growth retardation, truncal obesity, facial asymmetry, hypotonia, small phallus, malformed low-set ears and micrognathia']",,,,C0265505,,,,C548012,758.89,,,
mondo:0022993,dipsogenic diabetes insipidus,"['primary polydipsia', 'Dipsogenic diabetes insipidus']",0081058,,,C0268813,,C129735,,C548013,,,,
mondo:0022998,distal arthrogryposis Moore weaver type,['Moore Weaver syndrome'],,,,C2931342,,,,C536814,,,,
mondo:0022999,distichiasis heart congenital anomalies,,,,,,,,,,,,,
mondo:0023002,double discordia,"['corrected transposition', 'atrio-ventricular and ventriculo-arterial double Discordia']",,,,,,,,,,,,
mondo:0023003,double fingernail of fifth finger,,,,,,,,,,,,,
mondo:0023005,double uterus-hemivagina-renal agenesis,,,,,,,,,,,,,
mondo:0023006,doxorubicin induced cardiomyopathy,,,,,,,,,,,,,
mondo:0023007,Drachtman Weinblatt Sitarz syndrome,"['Drachtman Weinblatt Sitarz syndrome', 'marrow hypoplasia associated with congenital neurologic anomalies']",,,,C2930947,,,,C535603,,,,
mondo:0023011,Wilson-Mikity syndrome,"['Pulmonary dysmaturity syndrome', 'Wilson-Mikity syndrome', 'Pulmonary dysmaturity']",,,,C0270171,,,,,,,,
mondo:0023013,Duker-Weiss-Siber syndrome,"['Duker Weiss Siber syndrome', 'microphthalmos, microencephaly, mental retardation, agenesis of the corpus callosum, hypospadius, and cryptorchidism', 'microphthalmos, microencephaly, intellectual disability, agenesis of the corpus callosum, hypospadius, and cryptorchidism']",,,,C2930993,,,,C535719,,,,
mondo:0023015,duodenal atresia tetralogy of fallot,,,,,,,,,,,,,
mondo:0023016,duplication of leg mirror foot,,,,,,,,,,,,,
mondo:0023017,duplication of the thumb unilateral biphalangeal,,,,,,,,,,,,,
mondo:0023018,dupont sellier chochillon syndrome,,,,,,,,,,,,,
mondo:0023019,dwarfism bluish sclerae,,,,,,,,,,,,,
mondo:0023020,dwarfism deafness retinitis pigmentosa,,,,,,,,,,,,,
mondo:0023021,dwarfism lethal type advanced bone age,,,,,,,,,,,,,
mondo:0023022,dwarfism thin bones multiple fractures,,,,,,,,,,,,,
mondo:0023023,neonatal dacryocystitis,"['Neonatal Dacryocystitis', 'Neonatal dacryocystitis', 'neonatal dacryocystitis']",,,,C0270178,,C116819,,,,,,
mondo:0023030,dysmorphism cleft palate loose skin,,,,,,,,,,,,,
mondo:0023035,Eagle syndrome,"['elongated styloid process syndrome', 'styloid-stylohoid syndrome', 'Eagle^s syndrome', 'elongated styloid process which causes cervico facial pain tinnitus and otalgia']",,,,,,,,C538010,733.99,,,
mondo:0023038,eccentrochondrodysplasia,,,,,C0026707,,,,,,,,
mondo:0023039,eccrine mucinous carcinoma,,,,,C0346020,,,,,,,,
mondo:0023040,ectodermal dysplasia Bartalos type,,,,,,,,,,,,,
mondo:0023041,ectodermal dysplasia Berlin type,,,,,,,,,,,,,
mondo:0023042,ectodermal dysplasia margarita type,,,,,,,,,,,,,
mondo:0023043,ectodermal dysplasia alopecia preaxial polydactyly,"['absence of body & scalp hair, rounded nails, thin dental enamel, preaxial polydactyly of the feet, and unusual facial appearance']",,,,C2931691,,,,C538016,,,,
mondo:0023045,ectodermal dysplasia arthrogryposis diabetes mellitus,,,,,,,,,,,,,
mondo:0023046,ectodermal dysplasia blindness,,,,,,,,,,,,,
mondo:0023048,ectodermal dysplasia neurosensory deafness,,,,,C1857068,,,,,,,,
mondo:0023050,ectrodactyly cardiopathy dysmorphism,"['Van Den Ende Brunner syndrome', 'ectrodactyly of lower limbs, congenital heart defect and characteristic facies']",,,,C2931127,,,,C536187,,,,
mondo:0023054,klumpke^s paralysis,"['Klumpke Palsy', 'Lower brachial plexus palsy', 'Klumpkes Palsy', 'Dejerine Klumpke Palsy', 'Paralysis of the Lower Brachial Plexus', 'Palsy, Dejerine-Klumpke', 'Klumpke-DC)jerine paralysis', 'Dejerine-Klumpke Palsy', 'Klumpke-Dejerine paralysis', 'Dejerine-Klumpke palsy', 'Palsy, Klumpke^s', 'Paralysis, Klumpke', 'Klumpke-DC)jerine brachial plexus injury', 'Klumpke^s paralysis', 'Klumpke Paralysis', 'Klumpke^s Palsy', 'Klumpke^s palsy', 'Lower Brachial Plexus Palsy', 'Klumpke paralysis']",,,,C0270898,,C116724,,,,,,
mondo:0023059,Elliott ludman Teebi syndrome,"['multiple congenital anomalies, severe psychomotor retardation and symmetrical circumferential skin creases of arms and legs']",,,,C2931128,,,,C536204,,,,
mondo:0023061,enamel hypoplasia cataract hydrocephaly,,,,,,,,,,,,,
mondo:0023062,encephalocele anencephaly,,,,,,,,,,,,,
mondo:0023066,enchondromatosis dwarfism deafness,['Wallis cremin Beighton syndrome'],,,,,,,,,,,,
mondo:0023067,endemic Kaposi sarcoma,"['African Kaposi sarcoma', 'African/endemic Kaposi sarcoma']",,,,,,,,,,,,
mondo:0023068,engelhard yatziv syndrome,,,,,,,,,,,,,
mondo:0023069,enlarged vestibular aqueduct syndrome,"['large vestibular aqueduct syndrome', 'enlarged vestibular aqueduct']",0050332,,,,,,,,,,,
mondo:0023071,enterovirus antenatal infection,,,,,,,,,,,,,
mondo:0023073,eosinophilic cryptitis,['eosinophilic cystitis'],,,,C0742965,,,,,595.89,,,
mondo:0023076,eosinophilic pustular folliculitis,"['eosinophilic folliculitis', 'Ofuji^s disease', 'Ofuji disease', 'EPF', 'eosinophilic folliculitis, pustular']",,,,C0406305,,,,C535953,704.8,,,
mondo:0023079,epidermal nevus vitamin D resistant rickets,,,,,,,,,,,,,
mondo:0023083,epimetaphyseal dysplasia cataract,,,,,,,,,,,,,
mondo:0023084,epiphyseal dysplasia dysmorphism camptodactyly,,,,,,,,,,,,,
mondo:0023089,erythroplakia,['erythroplakia'],,,,C0014818,,C3025,1001786,,,,,
mondo:0023091,esophageal atresia coloboma talipes,,,,,,,,,,,,,
mondo:0023093,exertional headache,"['primary Exertional headache', 'primary headache associated with sexual activity']",,,,,,,,,,,,
mondo:0023094,exogenous ochronosis,"['ocular ochronosis', 'pseudo-ochronosis', 'exogenous ochronosis', 'ochronosis, acquired']",,,,,,,,C531762,270.2,,,
mondo:0023098,extrasystoles short stature hyperpigmentation microcephaly,['Char douglas Dungan syndrome'],,,,,,,,,,,,
mondo:0023099,FRAXD syndrome,['FRAXD'],,,,,,,,,,,,
mondo:0023100,facial clefting corpus callosum agenesis,,,,,,,,,,,,,
mondo:0023101,facio digito genital syndrome recessive form,,,,,,,,,,,,,
mondo:0023102,facio skeletal genital syndrome rippberger type,['Ripperger Aase syndrome'],,,,,,,,,,,,
mondo:0023106,Fairbank disease,"['epiphyseal dysplasia, Fairbank type', 'Fairbank multiple epiphyseal dysplasia', 'epiphyseal dysplasia Fairbank type', 'dysplasia epiphysealis multiplex', 'epiphyseal dysplasia, ribbing type']",,,,,,,,C536393,,,,
mondo:0023111,familial capillaro-venous leptomeningeal angiomatosis,,,,,C2931262,,,,C536609,,,,
mondo:0023113,familial colorectal cancer,"['colorectal cancer, familial', 'hereditary colorectal cancer']",,,,CN029768,"['0.02283', '0.05112', '-0.01938', '-0.03065', '0.01695', '-0.07666', '0.02242', '0.06903', '-0.05478', '-0.02269', '0.004055', '-0.00949', '-0.002222', '-0.002525', '-0.05624', '-0.06094', '-0.00904', '-0.03072', '-0.01642', '-0.0989', '-0.00643', '-0.03317', '0.05243', '-0.05258', '0.0317', '-0.01465', '0.005985', '-0.01168', '-0.014694', '-0.0494', '0.06192', '-0.010895', '0.0597', '0.01274', '0.00975', '-0.005352', '-0.04727', '-0.02565', '-0.00139', '-0.03084', '0.02861', '-0.05283', '0.02388', '-0.0508', '0.01113', '-0.04144', '-0.02086', '0.04764', '0.02888', '0.007755', '-0.002243', '0.00661', '-0.0008707', '0.0231', '-0.0454', '-0.02084', '0.0442', '-0.0422', '-0.1047', '-0.01239', '0.07196', '0.0288', '0.01264', '-0.007122', '-0.0006833', '0.0343', '0.08417', '0.0458', '-0.04852', '0.067', '-0.04825', '-0.01234', '0.004333', '-0.02524', '0.03946', '0.03357', '0.006832', '0.00427', '-0.02724', '-0.04282', '-0.03357', '0.04025', '-0.0381', '0.03845', '-0.02893', '-0.04544', '0.03555', '0.05048', '0.08655', '-0.02159', '0.02113', '0.05994', '-0.001072', '0.001159', '0.119', '0.03857', '0.0717', '-0.08636', '-0.04446', '0.0222']",,,,,,,
mondo:0023119,familial myelofibrosis,,,,,C2931351,,,,C536848,,,,
mondo:0023121,familial partial paralysis,"['partial paralysis, familial']",,,,CN035928,,,,,,,,
mondo:0023122,familial prostate carcinoma,"['prostate cancer, familial, susceptibility to, autosomal dominant, somatic mutation', 'prostate cancer, susceptibility to, autosomal dominant, somatic mutation', 'prostate cancer, familial', 'familial prostate cancer', 'hereditary prostate cancer', 'prostate cancer, hereditary', 'prostate cancer, autosomal dominant, somatic mutation', 'hereditary prostate carcinoma', 'prostate cancer, somatic']",,176807,1331,CN036094,"['-0.106', '-0.07935', '-0.2218', '-0.0886', '-0.02472', '-0.234', '0.004074', '0.1428', '-0.1287', '-0.1604', '0.1287', '0.1545', '-0.2354', '0.07666', '-0.319', '-0.3313', '-0.2563', '-0.0494', '0.05228', '-0.2947', '0.04385', '-0.1715', '0.1282', '-0.3762', '0.2162', '-0.1575', '0.199', '-0.10815', '-0.00662', '-0.4673', '0.2605', '-0.159', '0.3655', '-0.2617', '0.08716', '-0.1255', '-0.07526', '-0.1952', '0.064', '0.2034', '0.267', '-0.175', '0.1809', '-0.324', '0.02171', '-0.05133', '-0.26', '0.01404', '0.0658', '0.2712', '-0.00287', '0.3323', '0.1597', '0.137', '-0.0692', '-0.01595', '0.1544', '-0.0648', '-0.5425', '-0.1799', '0.3472', '0.3794', '0.1174', '-0.1727', '-0.004105', '0.4377', '0.2119', '0.528', '-0.1715', '0.343', '-0.0638', '-0.119', '0.003162', '-0.10895', '0.2418', '-0.1016', '0.0808', '0.2837', '-0.1283', '-0.2083', '-0.588', '0.2615', '-0.106', '-0.0641', '-0.1554', '-0.2742', '0.413', '-0.05078', '0.2177', '-0.2053', '-0.03015', '0.1389', '-0.111', '-0.1014', '0.61', '0.003195', '0.2522', '-0.0905', '-0.2468', '-0.1109']",C103817,,,,,,
mondo:0023124,familial pulmonary arterial hypertension leucopenia and atrial septal defect,"['familial pulmonary arterial hypertension, leucopenia and ASD', 'familial PAH, leucopenia and ASD']",,,,,,,,,,,,
mondo:0023129,Fara Chlupackova syndrome,['familial oto-facio-cervical dysmorphia'],,,,C2931416,,,,C537074,,,,
mondo:0023133,Faye-Petersen-Ward-Carey syndrome,,,,,C2931417,,,,C537076,,,,
mondo:0023134,febrile ulceronecrotic Mucha-Habermann disease,"['FUMHD', 'variant of Mucha-Habermann disease', 'ulceronecrotic Mucha-Habermann disease', 'A severe variant of pityriasis lichenoides et varioliformis acuta (PLEVA)']",,,,C1274297,,,,C537077,,,,
mondo:0023137,feigenbaum Bergeron syndrome,,,,,,,,,,,,,
mondo:0023138,Feingold trainer syndrome,"['unusual facies, cleft palate, short stature, and intellectual disability', 'unusual facies, cleft palate, short stature, and mental retardation']",,,,C2931126,,,,C536179,,,,
mondo:0023140,fenton Wilkinson Toselano syndrome,,,,,,,,,,,,,
mondo:0023142,fetal brain disruption sequence,,,,,,,,,,,,,
mondo:0023143,fetal enterovirus syndrome,,,,,,,,,,,,,
mondo:0023147,fetal parainfluenza virus type 3 syndrome,['Human respirovirus 3 caused infectious embryofetopathy'],,,,,,,,,,,,
mondo:0023148,fetal phenothiazine syndrome,,,,,,,,,,,,,
mondo:0023149,infection due to clostridium perfringens,"['C. perfringens infection', 'Infections, Clostridium perfringens', 'Infection caused by Clostridium perfringens', 'Infection, Clostridium perfringens', 'Clostridium perfringens infection', 'Infection due to Clostridium perfringens', 'Clostridium perfringens Infection', 'Clostridium perfringens Infections']",,,,C0275619,,,,,,,,
mondo:0023152,fibrocartilaginous embolism,"['embolism, fibrocartilaginous']",,,,C2931666,,,,C537927,,,,
mondo:0023153,tuberculous ascites,['tuberculous ascites'],,,,C0275919,,C27076,,,,,,
mondo:0023154,fibromatosis multiple non ossifying,"['Jaffe Campanacci syndrome', 'disseminated nonossifying fibromas in association with cafe-au-lait spots']",,,,C0796000,,,,,,,,
mondo:0023155,fibula aplasia complex brachydactyly,,,,,,,,,,,,,
mondo:0023157,fibular hypoplasia scapulo pelvic dysplasia absent,,,,,,,,,,,,,
mondo:0023158,Fitz-Hugh-Curtis syndrome,"['perihepatitis syndrome', 'gonococcal perihepatitis']",,,,,,,,C537936,,,,
mondo:0023161,viral myocarditis,"['Viral Myocarditis', 'Viral myocarditis', 'viral myocarditis']",,,,C0276138,,C128381,,,,,,
mondo:0023164,viral pericarditis,"['viral pericarditis', 'Viral pericarditis', 'Viral Pericarditis']",,,,C0276139,,C128405,,,,,,
mondo:0023165,florid cystic endosalpingiosis of the uterus,"['intramural florid cystic endosalpingiosis of the uterus', 'cystic endosalpingiosis of the uterus', 'intramural florid cystic endosalpingiosis in lower uterine segment of the uterus']",,,,C2931410,,,,C537064,,,,
mondo:0023167,focal alopecia congenital megalencephaly,,,,,,,,,,,,,
mondo:0023170,focal or multifocal malformations in neuronal migration,,,,,,,,,,,,,
mondo:0023171,foix chavany Marie syndrome,"['opercular syndrome, anterior', 'pseudobulbar paralysis, cortical type', 'anterior opercular syndrome', 'bilateral anterior opercular syndrome', 'congenital Foix-Chavany-Marie syndrome (subtype)', 'facio-Labio-pharyngo-Glosso-laryngo-brachial paralysis', 'facio-pharyngo-glossal diplegia with automatic-voluntary movement dissociation', 'congenital Foix-Chavany-Marie syndrome']",,,2048,C2931412,,,,C537069,,,,
mondo:0023175,Fontaine farriaux blanckaert syndrome,,,,,,,,,,,,,
mondo:0023176,formaldehyde poisoning,"['Formalin toxicity', 'formaldehyde toxicity', 'formaldehyde exposure', 'Formalin intoxication']",,,,,,,,C537268,,,,
mondo:0023178,fragile X syndrome type 1,,,,,,,,,,,,,
mondo:0023179,fragile X syndrome type 2,,,,,,,,,,,,,
mondo:0023180,fragile X syndrome type 3,,,,,,,,,,,,,
mondo:0023182,Franceschini Vardeu Guala syndrome,,,,,C2931463,,,,C537272,,,,
mondo:0023186,Fraser Jequier Chen syndrome,"['chondrodysplasia, situs inversus totalis, cleft epiglottis and larynx, hexadactyly of hands and feet, pancreatic cystic dysplasia, renal dysplasia/abs']",,,,C2930912,,,,C535481,,,,
mondo:0023188,Freiberg disease,"['Freiberg^s infraction', 'Freiberg-Kohler syndrome', 'Osteochondrosis of the metatarsal head, usually the second', 'Freiberg^s disease', 'Kohler^s second disease', 'second metatarsal osteochondrosis']",,,564003,C0264099,,,,C535636,,,,
mondo:0023193,Friedman Goodman syndrome,,,,,,,,,,,,,
mondo:0023194,frints de Smet Fabry Fryns syndrome,['Symbrachydactyly of the hand and foot'],,,,,,,,C538062,,,,
mondo:0023196,frontonasal malformation cloacal exstrophy,['fronto nasal malformation cloacal exstrophy'],,,,,,,,,,,,
mondo:0023197,frontonasal dysplasia Klippel feil syndrome,,,,,,,,,,,,,
mondo:0023199,frontonasal dysplasia phocomelic upper limbs,,,,,,,,,,,,,
mondo:0023200,Fryns Fabry Remans syndrome,,,,,,,,,,,,,
mondo:0023201,Fryns Smeets Thiry syndrome,,,,2058,,,,,,,,,
mondo:0023203,Fuchs atrophia gyrata chorioideae et retinae,,,,,,,,,C538071,,,,
mondo:0023204,Fukuda-Miyanomae-Nakata syndrome,"['Fukuyama type muscular dystrophy', 'muscular dystrophy, congenital, with central nervous system involvement', 'FCMD', 'Cerebromuscular dystrophy, Fukuyama type', 'muscular dystrophy, congenital progressive, with intellectual disability', 'muscular dystrophy, congenital, Fukuyama type', 'muscular dystrophy, congenital progressive, with mental retardation']",,,272,CN776933,,,,,,,,
mondo:0023206,functional pancreatic neuroendocrine tumor,"['syndromic pancreatic neuroendocrine tumour', 'functioning pancreatic endocrine tumor', 'functioning pancreatic endocrine tumour', 'syndromic pancreatic NET', 'functioning well differentiated pancreatic endocrine tumor', 'functioning well-differentiated pancreatic NEN', 'functioning well differentiated pancreatic endocrine tumour', 'functional pancreatic NET', 'functioning well-differentiated NEN of pancreas', 'functioning well-differentiated pancreatic neuroendocrine neoplasm', 'functioning pancreatic neuroendocrine tumor', 'functioning well differentiated pancreatic endocrine neoplasm', 'syndromic pancreatic neuroendocrine tumor', 'functioning pancreatic neuroendocrine tumour', 'functioning PNET', 'functional pancreatic neuroendocrine tumor', 'functioning neuroendocrine tumor of pancreas', 'functioning well-differentiated neuroendocrine neoplasm of pancreas', 'functioning pancreatic NET', 'functioning neuroendocrine tumour of pancreas']",,,506060,C1708107,,C45840,,,,,,
mondo:0023208,Fuqua Berkovitz syndrome,,,,,,,,,,,,,
mondo:0023209,galactorrhoea-hyperprolactinaemia,"['hyperprolactinaemia', 'galactorrhoea-hyperprolactinaemia', 'galactorrhea-hyperprolactinemia']",,,,,,,,C535402,,,,
mondo:0023212,Garret-Tripp syndrome,"['mental retardation with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes^ disease of the hip', 'Garret Tripp syndrome', 'polydactyly alopecia seborrheic dermatitis', 'intellectual disability with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes^ disease of the hip', 'Intellecutal disability with postaxial polydactyly, congenital absence of hair, severe seborrhoeic dermatitis, and Perthes^ disease of the hip']",,,,C2930965,,,,C535646,,,,
mondo:0023214,gas bloat syndrome,['post-fundoplication syndrome'],,,,C2930966,,,,C535647,,,,
mondo:0023221,Gaucher ichthyosis restrictive dermopathy,,,,,,,,,,,,,
mondo:0023224,inherited reflex epilepsy,['hereditary reflex epilepsy'],,,,,,,,,,,,
mondo:0023226,gershinibaruch Leibo syndrome,,,,,,,,,,,,,
mondo:0023227,gestational diabetes insipidus,"['Gestagenic diabetes insipidus', 'diabetes insipidus gestational']",0081057,,,C2932666,,,,C548014,,,,
mondo:0023230,Ghose-Sachdev-Kumar syndrome,"['bilateral nanophthalmos, pigmentary retinal dystrophy, and angle closure glaucoma']",,,,C2974016,,,,C537803,,,,
mondo:0023232,giant cell myocarditis,"['GCM', 'giant cell myocarditis', 'idiopathic giant-cell myocarditis']",,,,C0264856,,C97055,,,,,,
mondo:0023238,giant mammary hamartoma,['giant hamartoma of the breast'],,,,C2931343,,,,C536818,,,,
mondo:0023240,gigantism advanced bone age hoarse cry,,,,,,,,,,,,,
mondo:0023243,glass-chapman-hockley syndrome,"['craniosynostosis-dysmorphism-brachydactyly syndrome', 'craniosynostosis - dysmorphism - brachydactyly', 'craniosynostosis brachydactyly']",,,1535,C4303810,,,,,,,,
mondo:0023246,linear porokeratosis,"['Porokeratosis, Linear', 'Congenital facial linear porokeratosis (type)', 'Linear porokeratosis', 'Zosteriform porokeratosis', 'Linear Porokeratosis']",,,,C0302319,,,,,,,,
mondo:0023249,polyarticular juvenile rheumatoid arthritis,"['Juvenile polyarthritis rheumatoid factor positive', 'Juvenile polyarthritis rheumatoid factor negative', 'Polyarticular juvenile rheumatoid arthritis']",,,,C0311221,,,,,,,,
mondo:0023250,global disaccharide intolerance,,,,,,,,,,,,,
mondo:0023255,glossopalatine ankylosis micrognathia ear anomalies,,,,,,,,,,,,,
mondo:0023258,glycogen storage disease type 1 due to SLC37A4 mutation,"['SLC37A4 glycogen storage disease I', 'glucose-6-phosphate translocase deficiency', 'G6P translocase deficiency', 'glycogen storage disease I caused by mutation in SLC37A4']",,,,C2931345,,,,C536831,,,,
mondo:0023263,glyceraldehyde-3-phosphate dehydrogenase deficiency,['GAPDH deficiency'],,,,C1291264,,,,C536837,,,,
mondo:0023267,goldstein hutt syndrome,"['trichomegaly, cataract, and hereditary spherocytosis', 'long eyelashes, cataract, and hereditary spherocytosis']",,,,C2931465,,,,C537282,,,,
mondo:0023272,goniodysgenesis intellectual disability short stature,,,,,,,,,,,,,
mondo:0023273,pigmented dermatofibrosarcoma protuberans,"['Pigmented dermatofibrosarcoma protuberans of skin', 'Pigmented dermatofibrosarcoma protuberans', 'Pigmented DFSPs', 'Bednars Tumor', 'Pigmented dermatofibrosarcoma', 'Pigmented storiform neurofibroma', 'bednar tumor', 'bednar tumour', 'pigmented dermatofibrosarcoma protuberans (bednar tumor)', 'Pigmented Dermatofibrosarcoma Protuberans', 'Protuberan, Pigmented Dermatofibrosarcoma', 'Bednars Tumour', 'pigmented dermatofibrosarcoma protuberans', 'Bednar Tumour', 'Dermatofibrosarcoma Protuberans, Pigmented', 'Pigmented DFSP', 'Dermatofibrosarcoma Protuberan, Pigmented', 'DFSPs, Pigmented', 'Pigmented Dermatofibrosarcoma Protuberans (Bednar Tumor)', 'DFSP, Pigmented', 'Bednar^s Tumor', 'Protuberans, Pigmented Dermatofibrosarcoma', 'Bednar^s Tumour', 'Pigmented Dermatofibrosarcoma Protuberan', 'Tumor, Bednar^s', 'Bednar Tumor', 'Tumor, Bednar']",,,,C0334464,,C9430,,,,,,
mondo:0023275,Graham-Boyle-Troxell syndrome,"['cystic hamartoma of lung and kidney', 'Graham-Boyle-Troxell syndrome', 'cystic hamartomata of lung and kidney']",,,2111,C2931468,,,,C537292,759.6,,,
mondo:0023282,granulomatous hypophysitis,['idiopathic granulomatous hypophysitis'],,,,,,,,,,,,
mondo:0023283,ovarian granulosa cell tumor,"['ovary granulosa cell tumor', 'granulosa theca cell tumour', 'granulosa theca cell tumor', 'granulosa cell neoplasm of the ovary', 'granulosa cell tumour of the ovary', 'granulosa theca cell tumor of the ovary', 'granulosa cell tumor of ovary', 'ovary granulosa cell tumour', 'granulosa cell tumour of ovary', 'granulosa cell tumor of the ovary', 'adult granulosa cell tumor of the ovary', 'granulosa cell neoplasm of ovary', 'ovarian granulosa cell tumor', 'adult granulosa cell tumour of the ovary', 'granulosa theca cell tumour of the ovary', 'GCT of the ovary', 'ovarian granulosa cell neoplasm']",,,,C1370419,,C6261,1000421,C537296,,,,
mondo:0023286,graphite pneumoconiosis,['carbon pneumoconiosis'],,,,C0264439,,,,,503,,,
mondo:0023288,green sandford davison syndrome,"['anal anomalies, renal tract abnormalities, genital malformations, and syndactyly', 'renal and anogenital malformations with syndactyly']",,601446,,C2931777,,,,C538221,,,,
mondo:0023290,grix Blankenship Peterson syndrome,"['craniofacial and osseous defects mental retardation', 'craniofacial and osseous defects intellectual disability']",,,,,,,,,,,,
mondo:0023297,guttate psoriasis,['psoriasis guttate'],,,,C0343052,,,,,696.1,L40.4,,
mondo:0023305,heavy metal poisoning,"['heavy metal poisoning', 'chronic heavy metal poisoning', 'heavy metal toxicity']",,,,,,,1001518,D000075322,985.8,,,
mondo:0023368,Ho-Kaufman-McAlister syndrome,"['Ho Kaufman McAlister syndrome', 'cleft palate, micrognathia, Wormian bones, congenital heart disease, dislocated hips, absent tibiae, bowed fibulae, preaxial polydactyly of the feet']",,,,C2931819,,,,C538325,,,,
mondo:0023369,disorder of facial skeleton,"['facial skeleton disease or disorder', 'facial skeleton disease', 'maxillo-facial disease', 'maxillofacial anomaly', 'disease of facial skeleton', 'disorder of facial skeleton']",,,,,,,,,,,,
mondo:0023370,neoplastic disease or syndrome,,,,,,,,,,,,,
mondo:0023388,pityriasis rotunda,['Pityriasis rotunda'],,,,C0343060,,,,,,,,
mondo:0023415,congenital candidiasis,"['Congenital candidiasis', 'Congenital candidosis', 'Congenital Candidiasis', 'congenital candidiasis']",,,,C0343875,,C116811,,,,,,
mondo:0023419,hyperprolinemia,"['proline hydrogenase deficiency', 'hyperprolinemia type 1', 'proline oxidase deficiency']",0080541,,,C0268528,,,,,270.8,,,
mondo:0023472,chondrodysplasia situs inversus imperforate anus polydactyly,['impossible syndrome'],,,,,,,,,,,,
mondo:0023483,infectious myositis,"['infective myositis', 'infectious myositis']",,,,,,C26984,,,728.0,,,
mondo:0023510,Jaffer-Beighton syndrome,"['arachnodactyly, joint laxity, and spondylolisthesis', 'Jaffer Beighton syndrome']",,,,C2931533,,,,C537561,,,,
mondo:0023513,Jeune syndrome situs inversus,,,,,C2931535,,,,C537572,,,,
mondo:0023521,Judge Misch wright syndrome,"['keratodermia palmoplantar periorificial', 'dry skin, photophobia hyperkeratosis, abnormal fingernails', 'palmoplantar and perioroficial keratoderma with corneal epithelial dysplasia']",,,,C2931590,,,,C537692,,,,
mondo:0023528,KSHV inflammatory cytokine syndrome,"['KSHV inflammatory cytokine syndrome', 'KICS', 'Kaposi-sarcoma associated Herpesvirus (KSHV) inflammatory cytokine syndrome']",,,,C4086533,,C125711,,,,,,
mondo:0023530,kallikrein hypertension,['kallikrein attenuated hypertension'],,,,C1171349,,,,C537707,,,,
mondo:0023538,Kaplowitz-Bodurtha syndrome,"['congenital hypopituitarism and microphthalmia', 'hypopituitarism microphthalmia']",,,,C2931361,,,,C536893,,,,
mondo:0023540,Kashani-Strom-Utley syndrome,"['Kashani Strom Utley syndrome', 'hypoplastic pulmonary arteries and aorta with obstructive uropathy', 'pulmonary aortic stenosis obstructive uropathy']",,,1137,C2931392,,,,C537010,,,,
mondo:0023541,Kasznica-Carlson-Coppedge syndrome,"['Kasznica Carlson Coppedge syndrome', 'ectrodactyly spina bifida cardiopathy', 'ectrodactyly, retrognathism, abnormal ears, highly arched palate, spina bifida, congenital heart defect, single umbilical artery']",,,,C2931393,,,,C537011,,,,
mondo:0023543,Katsantoni-Papadakou-Lagoyanni syndrome,"['Trichodermal syndrome and intellectual disability', 'Trichodermal syndrome and mental retardation', 'Katsantoni Papadakou Lagoyanni syndrome']",,,,C2931394,,,,C537012,,,,
mondo:0023551,C1q nephropathy,['C1q nephropathy'],,,,C0403434,,,,,,,,
mondo:0023554,acquired testicular failure,['acquired testicular failure'],,,,C0403818,,C131091,,,,,,
mondo:0023557,infective vaginitis,"['PV - Vaginal infection', 'Infective vaginitis', 'Vaginal Infection', 'vaginal infection', 'Vaginal infection']",,,,C0404521,,C84353,,,,,,
mondo:0023558,Kocher-debre-Semelaigne syndrome,"['association of muscular pseudohypertrophy and hypothyroidism in children', 'Kocher debre Semelaigne disease']",,,,,,,,C537211,,,,
mondo:0023561,Koone-Rizzo-Elias syndrome,"['ichthyosis, intellectual disability and asymptomatic spasticity', 'ichthyosis, mental retardation and asymptomatic spasticity', 'Koone Rizzo Elias syndrome']",,,,C2931397,,,,C537023,,,,
mondo:0023563,Kotzot-Richter syndrome,"['oculocutaneous albinism, immunodeficiency, hematological disorders, and minor anomalies', 'albinism with immune and hematologic defects', 'oculocutaneous albinism, immunodeficiency, haematological disorders, and minor anomalies']",,203285,,C2931399,,,,C537025,,,,
mondo:0023567,Kozlowski Brown Hardwick syndrome,"['unusual facies, hooked clavicles, 13 pairs of ribs, widened metaphyses, square shaped vertebral bodies and communicating hydrocephalus']",,,,C2931511,,,,C537506,,,,
mondo:0023569,Kozlowski Ouvrier syndrome,"['agenesis of the corpus callosum with intellectual disability and osseous lesions', 'agenesis of the corpus callosum with mental retardation and osseous lesions']",,,,C2931512,,,,C537508,,,,
mondo:0023571,Kozlowski Rafinski Klicharska syndrome,['metaphyseal and epiphyseal dysplasia with unusual facies and cataract'],,,,C2931513,,,,C537509,,,,
mondo:0023573,Kozlowski Warren Fisher syndrome,"['cloverleaf skull generalized bone dysplasia', 'cloverleaf skull generalised bone dysplasia']",,,,C2931546,,,,C537614,,,,
mondo:0023575,Krauss Herman Holmes syndrome,"['telecanthus, hypertelorism, strabismus, and pes cavus syndrome']",,,,C2931549,,,,C537618,,,,
mondo:0023577,Krieble Bixler syndrome,['autosomal dominant blepharophimosis with multiple congenital anomalies'],,,,C2931550,,,,C537619,,,,
mondo:0023579,Kuster Majewski Hammerstein syndrome,"['alopecia, macular degeneration, and growth retardation', 'alopecia macular degeneration growth retardation']",,,,C2931740,,,,C538125,,,,
mondo:0023581,Kuster syndrome,"['cleft lip and palate, lower lip pits, and limb deficiency defects', 'cleft lip palate lip pits limb deficiency']",,,,C2931741,,,,C538126,,,,
mondo:0023595,congenital myotonic dystrophy,"['dystrophy, Congenital Myotonic', 'congenital myotonic dystrophy', 'Congenital Myotonic dystrophy', 'MYOTONIC dystrophy CONGEN', 'Congenital Myotonic dystrophies', 'Myotonic dystrophies, Congenital', 'dystrophies, Congenital Myotonic', 'Congenital myotonic dystrophy', 'Myotonic dystrophy, Congenital']",,,,C0410226,,C123308,,,,,,
mondo:0023597,laryngeal papillomatosis,"['Warts in the throat', 'juvenile laryngeal papillomatosis (subtype)', 'recurrent laryngeal papillomatosis', 'recurrent laryngeal papillomatosis (subtype)', 'juvenile laryngeal papillomatosis']",,,,C0396072,,C157733,,C537876,,,,
mondo:0023599,mesomelic dysplasia,"['mesomelic dysplasia', 'Mesomelic dwarf', 'mesomelic dysplasias', 'Mesomelic dysplasia', 'Mesomelic Dysplasia']",,,,C0410536,,C121156,,,,,,
mondo:0023601,non-classic congenital adrenal hyperplasia,"['late-onset congenital adrenal hyperplasia', 'attenuated congenital adrenal hyperplasia', 'non-classic congenital adrenal hyperplasia', 'non classic congenital adrenal hyperplasia', 'NCCAH', 'LOCAH']",,,,C0342467,,C131442,,C537877,,,,
mondo:0023603,hereditary disorder of connective tissue,"['Inherited disorder of connective tissue', 'connective tissue hereditary disorder', 'hereditary connective tissue disorder', 'Hereditary Connective Tissue Disorder', 'Mendelian connective tissue disorder']",,,,C0410787,,C97075,,,,,,
mondo:0023605,Laugier-Hunziker syndrome,"['LHS', 'Laugier and Hunziker pigmentation']",,,,C0406425,,,,,528.9,,,
mondo:0023607,Laurence-Prosser-Rocker syndrome,"['Hirschsprung^s disease associated with congenital heart malformation, broad big toes, and ulnar polydactyly', 'Hirschsprung^s disease associated with ulnar polydactyly, polysyndactyly of big toes and ventricular septal defect']",,,,C2931651,,,,C537882,,,,
mondo:0023609,le Marec-Bracq-Picaud syndrome,['complex malformation syndrome with brachymesomelia'],,,,C2931385,,,,C536997,,,,
mondo:0023619,lentigo maligna melanoma,"['Hutchison melanotic freckle', 'LMM', 'lentigo maligna melanoma', 'malignant lentigo melanoma', 'SKLMM']",,,,C2739810,,C9151,,,172.8,,,
mondo:0023628,levator syndrome,"['levator ani spasm syndrome', 'levator ani syndrome']",,,,,,C113615,,C535890,,,,
mondo:0023642,Weber syndrome,"['Midbrain stroke syndromes', 'Weber Syndrome', 'Weber-Gubler syndrome']",,,,C0455717,,,,,344.89,,,
mondo:0023644,lip and oral cavity carcinoma,"['oral cancer', 'oral carcinoma', 'lip and oral cavity cancer', 'lip and oral cavity carcinoma']",,,,C0220641,,C9315,,,,,,
mondo:0023646,lipodermatosclerosis,"['sclerosing panniculitis', 'hypodermitis sclerodermaformis', 'acute lipodermatosclerosis']",,,,C0406500,,,,C537026,,,,
mondo:0023650,littoral cell angioma of the spleen,['littoral cell angioma'],,,,C1627365,,,,C537031,,,,
mondo:0023655,"immunodeficiency 14b, autosomal recessive",['IMD14B'],,619281,,,,,,,,,,
mondo:0023657,"intellectual developmental disorder, autosomal dominant 65","['MRD65', 'mental retardation, autosomal dominant 65']",,619320,,,,,,,,,,
mondo:0023659,developmental and epileptic encephalopathy 96,['DEE96'],0070377,619340,,,,,,,,,,
mondo:0023660,"angioedema, hereditary, 6",['HAE6'],,619363,,,,,,,,,,
mondo:0023662,lymphatic malformation 10,['LMPHM10'],,619369,,,,,,,,,,
mondo:0023664,spermatogenic failure 54,['SPGF54'],0112335,619379,,,,,,,,,,
mondo:0023670,Bardet-Biedl syndrome 20,['BBS20'],0081009,619471,,,,,,,,,,
mondo:0023671,oculopharyngodistal myopathy 3,['OPDM3'],0081299,619473,,,,,,,,,,
mondo:0023679,hematohidrosis,"['Hematohidrosis', 'Hematidrosis']",,,,C0473554,,,,,705.89,,,
mondo:0023682,tympanic paraganglioma,"['Tympanic Paraganglioma', 'Glomus tympanicum tumour', 'Tympanic paraganglioma', 'Glomus Tympanicum Tumors', 'Glomus Tympanicum Tumours', 'Glomus Tympanicum Tumor', 'Glomus tympanicum paraganglioma', 'Tumor, Glomus Tympanicum', 'Glomus Tympanicum Tumour', 'tympanic paraganglioma', 'Tumors, Glomus Tympanicum', 'Glomus tympanicum tumor']",,,,C0474820,,C8428,,D043604,,,,
mondo:0023691,maple syrup urine disease type 1A,['MSUD type 1A'],,,,,,,,,,,,
mondo:0023692,maple syrup urine disease type 1B,"['MSUD type 3 (formerly)', 'MSUD type IB', 'MSUD due to deficiency of E1-beta subunit of branched-chain alpha-keto acid dehydrogenase complex']",,,,,,,,,,,,
mondo:0023693,maple syrup urine disease type 2,"['MSUD type 2', 'MSUD2']",,,,,,,,,,,,
mondo:0023696,Marinesco-Sjogren-like syndrome,"['juvenile cataract, cerebellar atrophy, intellectual disability, and myopathy', 'Marinesco-Sjogren-like syndrome (MSLS)', 'juvenile cataract, cerebellar atrophy, mental retardation, and myopathy']",,248810,,C0796036,,,,C535913,,,,
mondo:0023699,Maroteaux Fonfria syndrome,"['apert syndrome with polydactyly of hands and feet', 'apparent apert syndrome with polydactyly']",,,,C2931088,,,,C536023,,,,
mondo:0023704,Martinez Monasterio Pinheiro syndrome,"['cleft lip/palate oligodontia syndactyly hair alterations', 'cleft lip-palate-oligodontia-syndactyly-hair alterations']",,,,C2931089,,,,C536027,,,,
mondo:0023726,mediastinal yolk sac tumor,"['yolk Sac tumour of mediastinum', 'endodermal sinus tumor of mediastinum', 'mediastinum yolk sac tumour', 'mediastinal endodermal sinus tumours', 'mediastinal endodermal sinus tumour', 'mediastinal yolk Sac tumour', 'yolk Sac tumour of the mediastinum', 'mediastinum yolk sac tumor', 'mediastinal endodermal sinus neoplasm', 'endodermal sinus neoplasm of the mediastinum', 'mediastinal endodermal sinus tumor', 'yolk Sac tumor of the mediastinum', 'mediastinal yolk Sac neoplasm', 'endodermal sinus tumour of the mediastinum', 'yolk Sac neoplasm of mediastinum', 'endodermal sinus tumor of the mediastinum', 'mediastinal yolk Sac tumor', 'endodermal sinus neoplasm of mediastinum', 'endodermal sinus tumour of mediastinum', 'yolk Sac tumor of mediastinum', 'yolk Sac neoplasm of the mediastinum', 'mediastinal endodermal sinus tumors', 'EST']",,,,C1334683,,C6443,,,,,,
mondo:0023757,meralgia paresthetica,"['meralgia paraesthetica familial (type)', 'Bernhardt-Roth syndrome', 'lateral femoral cutaneous nerve entrapment']",,,,C0152110,,,,C537458,355.1,,,
mondo:0023809,Milner-Khallouf-Gibson syndrome,"['microcephaly, short stature, slow growth, beak nose, micrognathia, skin dyspigmentation and forearm and thumb dysplasia', 'Milner Khallouf Gibson syndrome']",,,,C2931503,,,,C537473,,,,
mondo:0023820,Moebius axonal neuropathy hypogonadism,['Moebius syndrome with hypogonadotrophic hypogonadism and progressive peripheral neuropathy axonal and demyelinating type'],,,,C2931024,,,,C535806,,,,
mondo:0023833,multifocal choroiditis,,,,,C1533060,,,,D000080364,,,,
mondo:0023865,corneal infection,"['infective keratitis', 'infection of cornea', 'keratitis caused by infection', 'corneal infection']",,,519278,C0729777,,C83813,,,,,,
mondo:0023868,melanoma associated retinopathy,"['Melanoma-Associated Retinopathy', 'Melanoma-Associated Retinopathies', 'Melanoma-associated retinopathy', 'Retinopathies, Melanoma-Associated', 'Melanoma Associated Retinopathy', 'Retinopathy, Melanoma-Associated', 'Melanoma associated retinopathy']",,,,C0730308,,,,,,,,
mondo:0023880,WHIM syndrome,,,,,,,,,,,,,
mondo:0023910,Martsolf syndrome,,,,,,,,,,,,,
mondo:0023961,"visceral neuropathy, familial",,,,,,,,,,,,,
mondo:0024171,radio-digito-facial dysplasia,['Van Goethem syndrome'],,,,,,,,,,,,
mondo:0024182,dry beriberi,['endemic neuritis'],0070318,,,,,,,,,,,
mondo:0024183,wet beriberi,,0070317,,,,,,,,,,,
mondo:0024189,"neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset",,,,,,,,,,,,,
mondo:0024193,"portal hypertension, noncirrhotic",,,,,,,,,,,,,
mondo:0024227,miliaria pustulosa,,0070319,,,,,,,,,,,
mondo:0024228,miliaria profunda,,0070320,,,,,,,,,,,
mondo:0024229,miliaria crystallina,,0070321,,,,,,,,,,,
mondo:0024234,Seckel like syndrome majoor-krakauer type,['Bird-headed dwarfism microcephaly micrognathia'],,,,,,,,,,,,
mondo:0024235,Brenner tumor,['Brenner tumor'],,,,,,C39954,,D001948,,,,
mondo:0024237,inherited neurodegenerative disorder,"['genetic neurodegenerative disease', 'hereditary neurodegenerative disorder', 'hereditary neurodegenerative disease']",,,183500,CN200549,,C97073,,D020271,,,,
mondo:0024238,cerebral degeneration,"['neurodegenerative disease of telencephalon', 'telencephalon neurodegenerative disease']",,,,C0154671,,,,,331.9,,,
mondo:0024239,congenital anomaly of cardiovascular system,"['disorder of cardiovascular system development', 'cardiovascular system development disease', 'congenital Abnormality of the circulatory system', 'congenital cardiovascular anomaly', 'congenital cardiovascular Abnormality']",,,,,,C35729,,,747.9,,,
mondo:0024240,eccrine carcinoma,"['eccrine sweat gland adenocarcinoma', 'eccrine sweat gland carcinoma', 'carcinoma of eccrine sweat gland', 'carcinoma, eccrine gland, malignant', 'eccrine adenocarcinoma', 'eccrine carcinoma', 'eccrine adenocarcinoma (morphologic abnormality)']",4920,,,C1707878,,C27255,,,,,,
mondo:0024245,ductal eccrine adenocarcinoma,"['ductal eccrine adenocarcinoma', 'eccrine ductal carcinoma of skin', 'ductal eccrine carcinoma', 'eccrine ductal carcinoma (morphologic abnormality)', 'primary mucoepidermoid cutaneous carcinoma', 'sweat gland carcinoma of the hand', 'malignant hidradenoma', 'anaplastic syringoma', 'hidradenocarcinoma', 'eccrine ductal carcinoma', 'malignant acrospiroma']",5570,,,,,C43345,,,,,,
mondo:0024246,syringofibroadenoma,"['acrosyringeal adenomatosis', 'eccrine syringofibroadenoma', 'syringofibroadenoma', 'eccrine syringofibroadenomatous hyperplasia', 'acrosyringeal nevus']",,,,C1266060,,C43356,,,,,,0031018
mondo:0024247,benign eccrine neoplasm,"['benign eccrine skin tumor', 'benign eccrine neoplasm of skin', 'benign eccrine skin neoplasm', 'benign eccrine tumour of skin', 'benign eccrine tumor of skin', 'benign eccrine skin tumour', 'benign eccrine tumor of the skin', 'benign eccrine tumour', 'benign eccrine tumour of the skin', 'benign skin tumour with eccrine differentiation', 'eccrine sweat gland neoplasm, benign', 'benign eccrine neoplasm of the skin', 'benign eccrine tumor', 'benign eccrine neoplasm']",,,,C1332493,,C6797,,,,,,
mondo:0024249,pityriasis lichenoides,"['Pityriasis Lichenoides et Varioliformis Acuta', 'acute Pityriasis Lichenoides', 'Pityriasis Lichenoides, chronic', 'Pityriasis Lichenoides', 'Pityriasis Lichenoides, acute', 'Pityriasis Lichenoides chronica', 'chronic Pityriasis Lichenoides']",,,,,,C85013,,D017514,,,,
mondo:0024250,acute lichenoid pityriasis,"['Habermanns disease', 'Habermann^s disease', 'Habermann disease', 'Mucha-Habermann disease', 'PLEVA', 'disease, Habermann', 'disease, Habermann^s', 'Mucha Habermann disease', 'disease, Mucha-Habermann']",,,,,,,,,696.5,,,
mondo:0024251,Minamata disease,['Chisso-Minamata disease'],,,,CN200665,,,,,,,,
mondo:0024252,global developmental delay-neuro-ophthalmological abnormalities-seizures-intellectual disability syndrome,,,,488613,,"['-0.02835', '-0.1068', '-0.07086', '0.2261', '-0.5957', '-0.464', '0.775', '0.4653', '-0.01729', '-0.3315', '-0.2637', '-0.1764', '0.006336', '0.716', '-0.4385', '0.2269', '-0.1656', '-0.07605', '-0.1481', '-0.476', '-0.1304', '0.8916', '-0.2067', '-0.2252', '0.1453', '-0.1059', '-0.0948', '-0.006702', '-0.3455', '0.72', '0.0402', '0.04312', '0.478', '0.4155', '0.5806', '0.4119', '-0.1951', '-0.387', '0.0928', '-0.507', '-0.2072', '-0.2072', '-0.3845', '-0.3892', '0.2018', '-0.292', '-0.0421', '0.575', '0.3557', '0.7524', '-0.2686', '0.3315', '0.2283', '-0.7046', '-0.02394', '0.2106', '0.0689', '0.1699', '-0.3286', '-0.06198', '-0.4512', '0.3613', '0.5435', '-0.007866', '-0.83', '1.16', '0.0496', '-0.0361', '-0.8496', '0.8936', '0.193', '0.6807', '-0.0862', '-0.424', '0.348', '0.6655', '0.7354', '0.3591', '-0.1755', '-0.1035', '0.1813', '0.926', '0.5337', '0.2659', '0.503', '-0.02698', '-0.1927', '0.9556', '0.698', '1.363', '0.2308', '0.386', '0.1719', '0.1043', '-0.01886', '0.0866', '0.1829', '-0.3987', '0.1631', '0.521']",,,,,,,
mondo:0024257,hereditary motor neuron disease,"['genetic anterior horn cell disease', 'hereditary motor neuron disease', 'genetic motor neuron disease']",,,98505,CN207018,,,,,,,,
mondo:0024262,massive neonatal aspiration syndrome,,,,,,,,,,,,,
mondo:0024263,neonatal aspiration syndrome,,,,,C0349468,,C118312,,,,,,
mondo:0024264,"hypothyroidism, congenital, nongoitrous, 2","['congenital nongoitrous hypothyroidism 2', 'thyroid agenesis', 'hypothyroidism, congenital, due to thyroid dysgenesis', 'congenital hypothyroidism due to thyroid dysgenesis or hypoplasia', 'congenital nongoitrous hypothryoidism 2', 'resistance to thyrotropin', 'hypothyroidism, congenital, due to thyroid dysgenesis or hypoplasia', 'thyroid hypoplasia', 'thyroid, ectopic', 'hypothyroidism, athyreotic', 'athyreotic hypothyroidism', 'hypothyroidism, congenital, nongoitrous, 2', 'thyroid dysgenesis', 'thyrotropin resistance', 'CHNG2']",0070124,218700,95720,,"['-0.3381', '0.1125', '-0.06354', '-0.34', '0.2407', '-0.07623', '-0.1554', '0.4338', '-0.467', '-0.3486', '-0.0815', '-0.02162', '-0.2382', '0.2446', '-0.0326', '0.2622', '0.4805', '-0.2642', '-0.2013', '-0.87', '-0.3877', '0.11346', '0.9126', '-0.758', '0.4172', '0.331', '0.3853', '0.2456', '0.7725', '0.0946', '0.3582', '0.332', '0.2263', '0.4739', '-0.4797', '-0.1454', '-0.11786', '0.0826', '-0.0983', '0.1588', '0.4255', '0.1356', '-0.2211', '0.4172', '0.3425', '0.09625', '0.469', '0.0328', '0.4998', '0.1399', '0.0827', '-0.1458', '-0.3357', '-0.4475', '-0.5303', '0.1786', '0.1711', '-0.5356', '-0.3892', '-0.1031', '0.463', '0.0502', '-0.1691', '-0.4788', '-0.057', '0.2142', '0.5107', '0.325', '-0.4172', '0.2147', '0.00482', '0.4116', '-0.06354', '-0.573', '0.1855', '-0.06775', '0.6797', '-0.06192', '-0.4065', '-0.0826', '-0.3142', '-0.3137', '-0.4368', '-0.5034', '0.313', '0.1908', '-0.04865', '0.01389', '0.8506', '-0.2118', '0.1', '0.871', '0.1294', '0.1567', '0.633', '-0.0276', '-0.3428', '-0.09015', '0.44', '0.07825']",,,C566852,,,,
mondo:0024265,Duane syndrome type 1,"['Duane anomaly', 'DURS1', 'Drs', 'retraction syndrome', 'Duane syndrome', 'Duane retraction syndrome 1']",,126800,,,,,,,,,,
mondo:0024266,patent ductus arteriosus 3,"['patent ductus arteriosus 3', 'patent ductus arteriosus caused by mutation in PRDM6', 'PDA3', 'PRDM6 patent ductus arteriosus']",,617039,,,,,,,,,,
mondo:0024268,superficial mycosis,"['piedra', 'steroid-modified tinea infection', 'stratum corneum of epidermis fungal infectious disease']",0050133,,,C2980104,,,,,117.9,,,
mondo:0024270,parasitic intestinal disorder,"['intestinal disease, parasitic', 'parasitic intestinal disease', 'disease, parasitic intestinal', 'intestine parasitic infection', 'diseases, parasitic intestinal', 'parasitic intestinal diseases']",,,,C0021832,,,,D007411,,,,
mondo:0024271,intestinal helminthiasis,['intestine parasitic helminthiasis infectious disease'],,,,C0348287,,,,C531698,,,,
mondo:0024275,amebic dysentery,"['dysentery, amoebic', 'colitis, amebic', 'entamoebiasis, intestinal', 'amoebic Colitides', 'Colitides, amebic', 'amoebic dysentery due to Entamoeba histolytica', 'Entamoebiases, intestinal', 'amoebiasis, intestinal', 'intestinal Amebiases', 'amoebiasis due to Entamoeba histolytica', 'amebiasis, intestinal', 'amoebic dysentery', 'amebic colitides', 'dysenteries, amebic', 'intestinal Entamoebiases', 'amebic dysenteries', 'amebic dysentery', 'dysenteries, amoebic', 'Amebiases, intestinal', 'amebic colitis', 'intestinal entamoebiasis', 'amoebic dysenteries', 'amoebiases, intestinal', 'intestinal Amoebiases', 'intestinal amebiasis', 'Colitides, amoebic', 'amoebic colitis', 'intestinal amoebiasis', 'colitis, amoebic']",,,,,,C34558,,D004404,,,,
mondo:0024276,glandular cell neoplasm,"['glandular cell neoplasm', 'glandular cell tumor', 'glandular cell epithelial neoplasm', 'glandular cell tumour', 'glandular cell epithelium neoplasm']",,,,C1333820,,C7132,,,,,,0031493
mondo:0024277,neonatal thrombocytopenia,,,,,,,,,D054098,,,,
mondo:0024278,proctocolitis,"['colorectum inflammation', 'proctocolitis']",,,,C0033247,,C77952,,D011350,,,,
mondo:0024279,chronic endometritis,"['chronic endometritis', 'endometritis, chronic']",,,,C0238104,,C102820,,,,,,
mondo:0024280,polyarticular arthritis,"['polyarticular arthritis', 'polyarthritis']",,,,,,C26996,,,,,,
mondo:0024281,juvenile chronic polyarthritis,['juvenile chronic polyarthritis'],,,,,,C26979,,,,,,
mondo:0024282,mucinous ovarian cancer,"['malignant ovarian mucinous tumour', 'malignant ovarian mucinous neoplasm', 'ovarian mucinous neoplasm, malignant', 'malignant ovarian mucinous tumor']",,,,C1518233,,C40033,,,,,,
mondo:0024283,Demodex folliculitis,['hair follicle demodicidosis'],,,,C0392666,,,,,704.8,,,
mondo:0024284,demodicidosis of sebaceous gland,['sebaceous gland demodicidosis'],,,,,,,,,,,,
mondo:0024285,epsilon-heavy chain disease,,,,,C0272254,,,,,273.2,,,
mondo:0024286,benign blood vessel neoplasm,"['benign blood vessel neoplasm', 'benign blood vessel tumor', 'benign blood vessel tumour']",60006,,,C0685121,,C8537,,,,,,
mondo:0024287,congenital vascular malformation,"['congenital vascular malformation', 'vascular malformation']",,,,,,C112117,,,,,,
mondo:0024288,hyperbilirubinemia,,,,,C0020433,,,,D006932,,,,
mondo:0024290,enuresis,['enuresis'],,,,C0014394,,C34588,,D004775,,,,
mondo:0024291,vascular malformation,"['vascular malformation', 'malformations, vascular', 'malformation, vascular']",,,,,,,,D054079,,,,
mondo:0024292,gastrointestinal polyp,"['GI polyp', 'gastrointestinal polyp', 'gastrointestinal tract polyp']",,,,C0744333,,C35516,,,,,,
mondo:0024294,skin disorder caused by infection,"['infectious skin disease', 'diseases, infectious skin', 'skin disease, infectious', 'infectious skin diseases', 'disease, infectious skin']",,,,,,,,D012874,,,,
mondo:0024295,skin disease caused by bacterial infection,"['disease, bacterial skin', 'bacterial skin disease', 'diseases, bacterial skin', 'Bacteria caused skin disease caused by infection', 'bacterial skin diseases', 'skin disease, bacterial']",,,,,,,,D017192,,,,
mondo:0024296,vascular neoplasm,"['neoplasms, vascular', 'vascular tissue neoplasm', 'tumour of vascular system', 'tumour of vascular tissue', 'vascular neoplasm', 'vascular tumor', 'tumors, vascular', 'vascular tissue tumor', 'vascular system neoplasm (disease)', 'vascular tissue tumour', 'vascular tumors', 'vascular system tumour', 'vascular system tumor', 'vascular neoplasms', 'neoplasm of vascular tissue', 'vascular tumour', 'tumor of vascular tissue', 'neoplasm of vascular system', 'vascular tumours', 'tumor of vascular system']",,,,,,C7388,,,,,,
mondo:0024298,vitamin deficiency disorder,"['avitaminosis', 'vitamin deficiency disorder', 'deficiencies, vitamin', 'vitamin deficiency', 'Avitaminoses', 'vitamin deficiencies', 'deficiency, vitamin']",,,,C1510471,,C35772,0005878,D001361,269.2,,,
mondo:0024299,vitamin D-dependent rickets,['VDDR'],0080883,,,C0221468,,,,,,,,
mondo:0024300,hypophosphatemic rickets,"['rickets, vitamin D-resistant', 'Ricket, hypophosphatemic', 'vitamin D-resistant rickets', 'acquired vitamin D-resistant rickets', 'hypophosphatemic rickets', 'rickets, vitamin D resistant', 'Phosphopenic rickets', 'hypophosphatemia, vitamin D-resistant rickets', 'hypophosphatemic Ricket', 'acquired vitamin D resistant rickets', 'hypophosphatemic vitamin D-resistant rickets', 'hypophosphatemic vitamin D resistant rickets']",,,,,,C131449,,D063730,,,,
mondo:0024301,acquired mineral metabolism disease,"['acquired mineral metabolism disease', 'mineral metabolism disease']",0050032,,,,,,,,,,,
mondo:0024302,internal hirudiniasis,,,,,C0348999,,,,,,B83.4,,
mondo:0024303,external hirudiniasis,,,,,C0392037,,,,,,B88.3,,
mondo:0024304,ichthyosis vulgaris,"['common ichthyosis', 'fish scale disease', 'ichthyosis vulgaris']",,,,C0079584,,C84778,,D016112,,,,
mondo:0024305,acquired hyperprolactinemia,"['hyperprolactinemia', 'acquired hyperprolactinemia (disease)', 'Chiari-Frommel syndrome', 'pregnancy-related A-G syndrome']",12700,,,,,,,D006966,,E22.1,,
mondo:0024306,acquired lactic acidosis,"['lactic acidosis', 'acquired lactic acidosis']",3650,,,,,,1000036,D000140,,,,
mondo:0024307,prothrombin deficiency,,,,,,,,,,,,,
mondo:0024308,pseudoxanthoma elasticum (inherited or acquired),['PXE'],,,,,,,,,757.39,,,
mondo:0024309,"neuropathy, hereditary sensory and autonomic, type 2A","['hereditary sensory and autonomic neuropathy type 2A', 'neuropathy, hereditary sensory, type 2A', 'neuropathy, hereditary sensory and autonomic, type II', 'Morvan disease', 'neuropathy, hereditary sensory and autonomic, type IIA', 'acroosteolysis, Giaccai type', 'neuropathy, hereditary sensory radicular, autosomal recessive', 'HSAN2A', 'hereditary sensory and autonomic neuropathy type IIA', 'HSAN 2A', 'neuropathy, progressive sensory, of children', 'acroosteolysis, neurogenic', 'neuropathy, congenital sensory', 'HSN 2A']",0070155,201300,,C0751540,,,,,,,,
mondo:0024310,angiodysplasia of stomach,['stomach angiodysplasia'],,,,C0744273,,,,,,,,
mondo:0024311,cancer affecting bone of limb skeleton,"['limb bone cancer', 'malignant neoplasm of limb bone', 'cancer of limb bone', 'malignant limb bone neoplasm']",,,,,,,,,,C40,,
mondo:0024312,cancer of short bone of upper limb,,,,,,,,,,,C40.1,,
mondo:0024313,staphylococcal infection,['staphylococcal infection'],,,,,,C35038,,D013203,,,,
mondo:0024314,parasitemia,['Parasitemias'],,,,C0242723,,,,D018512,,,,
mondo:0024315,parasitic endophthalmitis,['parasitic endophthalmitis'],,,,C0014238,,C34587,,,360.13,,,
mondo:0024316,physiological malfunction arising from mental factor,['physiological malfunction arising from mental Factor'],,,,C0154548,,C35186,,,,,,
mondo:0024317,chronic pain syndrome,"['disorder involving pain, chronic']",,,,C1298685,,,,,338.4,G89.4,,
mondo:0024318,viral infection of central nervous system,,,,,C0348165,,,,D020805,,A80-A89,,
mondo:0024320,inner ear neoplasm,"['internal ear neoplasm (disease)', 'inner Ear neoplasm', 'neoplasm of internal ear', 'tumour of internal ear', 'tumor of internal ear', 'internal ear tumor', 'internal Ear neoplasm', 'internal ear tumour']",,,,C1512779,,C39784,,,,,,
mondo:0024321,disorder of GPI anchor biosynthesis,"['disorder of GPI anchor biosynthetic process', 'GPIBD']",,,,,,,,,,,,
mondo:0024322,disorder of glycosylation,"['glycosylation disease', 'disorder of glycosylation']",,,,,,,,,,,,
mondo:0024323,glomangiomyoma,['glomangiomyoma'],8020,,,C0334422,,C4223,,,,,,
mondo:0024325,cutaneous glomangiomyoma,"['zone of skin glomangiomyoma', 'glomangiomyoma of skin']",,,,C1275227,,,,,227.6,,,
mondo:0024326,pleural adenomatoid tumor,"['benign mesothelioma of pleura', 'pleural adenomatoid tumor', 'benign mesothelioma of the pleura', 'pleural mesothelioma, benign', 'pleura adenomatoid tumor', 'pleura adenomatoid tumour', 'pleural benign mesothelioma']",,,,,,C4499,,,,,,
mondo:0024327,chronic renal failure syndrome,"['chronic renal failure disease', 'kidney failure, chronic', 'Chronic renal disease', 'chronic renal failure', 'CRF - chronic renal failure']",,,,,,C9438,,D051436,585.9,,,
mondo:0024330,infectious otitis media,"['otitis media', 'middle Ear infection', 'acute otitis Media', 'infectious otitis Media', 'AOM']",,,,C2827407,,C84354,,,,,,
mondo:0024331,colorectal carcinoma,"['cancer of the large intestine', 'colorectal carcinoma', 'large intestine carcinoma', 'large bowel carcinoma', 'cancer of large intestine', 'cancer of the large bowel', 'carcinoma of large intestine', 'colorectal (colon or rectal) cancer', 'colorectal cancer', 'carcinoma of the large intestine', 'large bowel cancer', 'carcinoma of colorectum', 'large intestine cancer', 'cancer of large bowel', 'carcinoma of large bowel', 'carcinoma of the large bowel', 'CRC', 'colorectum carcinoma']",0080199,,,CN221574,,C2955,,,,,,
mondo:0024332,perennial allergic rhinitis,"['perennial allergic rhinitis', 'non-seasonal allergic rhinitis', 'nonseasonal allergic rhinitis']",,,,C0035457,,C92189,,D012221,,,,
mondo:0024333,sciatica,"['bilateral sciatica', 'sciatic neuralgia', 'sciatic Neuralgias', 'neuralgias, sciatic', 'neuralgia, sciatic', 'bilateral sciaticas', 'sciatica, bilateral']",,,,,,,,D012585,724.3,,,
mondo:0024334,peripheral nerve lesion,,,,,,,,,,,,,
mondo:0024335,retrobulbar neuritis,,,,,,,,,,,,,
mondo:0024336,vulvar adenocarcinoma,"['adenocarcinoma of vulva', 'vulva adenocarcinoma', 'mammalian vulva adenocarcinoma', 'vulvar adenocarcinoma', 'adenocarcinoma of the vulva']",2098,,494454,C1336975,,C6380,,,,,,
mondo:0024337,urothelial neoplasm,"['urothelium tumour', 'transitional cell neoplasm of the urinary tract', 'urothelium tumor', 'neoplasm of urothelium', 'urothelium neoplasm (disease)', 'urothelial neoplasm', 'tumor of urothelium', 'tumour of urothelium']",,,,C1519840,,C39852,,,,,,
mondo:0024338,mucinous neoplasm,"['mucinous neoplasm', 'mucinous tumor', 'mucinous tumour']",,,,C1334811,,C7070,,,,,,
mondo:0024339,lymph node neoplasm,"['lymph node tumor', 'lymph node neoplasm (disease)', 'neoplasm of lymph node', 'lymph node neoplasm', 'lymph node tumour', 'tumour of lymph node', 'tumor of lymph node']",,,,,,C35497,,,,,,
mondo:0024340,retinal neuroblastoma,"['neuroblastoma of retina', 'retinal neuroblastoma', 'neuroblastoma of the retina', 'retina neuroblastoma']",,,,,,C6956,,,,,,
mondo:0024341,retinal cell neoplasm,"['retinal cell tumour', 'retinal cell neoplasm', 'retinal cell tumor', 'retinal neural cell neoplasm']",,,,C1335765,,C7061,,,,,,
mondo:0024343,pityriasis simplex,,,,,,,,,,690.18,,,
mondo:0024344,pityriasis folliculorum,,,,,C0406312,,,,,696.5,,,
mondo:0024345,pityriasis streptogenes,,,,,,,,,,696.5,,,
mondo:0024346,pityriasis amiantacea,,,,,C0343100,,,,,696.5,,,
mondo:0024349,pityriasis alba,,,,,,,,,,696.5,,,
mondo:0024350,pityriasis steatoides,,,,,C1274781,,,,,696.5,,,
mondo:0024352,viral respiratory tract infection,['viral respiratory tract infection'],,,,,,C27219,,,519.8,,,
mondo:0024354,cytomegalovirus pneumonia,"['Cytomegalovirus caused pneumonia', 'Cytomegaloviral pneumonia', 'Cytomegalovirus pneumonia', 'CMV pneumonia']",,,,C0276253,,C35360,,,,,,
mondo:0024355,respiratory tract infectious disorder,"['respiratory infections', 'respiratory tract infection', 'infections, upper respiratory', 'upper respiratory tract infections', 'infection, respiratory tract', 'infections, upper respiratory tract', 'infections, respiratory tract', 'infections, respiratory', 'upper respiratory infections', 'respiratory infection, upper']",,,,,,,,D012141,519.8,,,
mondo:0024356,primary central sleep apnea syndrome,,,,,C0751762,,,,,327.21,G47.31,,
mondo:0024357,drug induced central sleep apnea,,,,,C3662033,,,,,,,,
mondo:0024358,complex sleep apnea,"['CompSAS', 'complex sleep apnea']",0080302,,,,,,,,,,,
mondo:0024359,central sleep apnea due to periodic breathing,,,,,C3662057,,,,,786.09,,,
mondo:0024360,central sleep apnea caused by high altitude,,,,,C4075997,,,,,,,,
mondo:0024361,circadian rhythm sleep disorder,['circadian sleep disorder'],,,,,,C95071,,D020178,327.30,G47.2,,
mondo:0024363,rapid eye movement sleep disorder,,,,,,,,,,379.59,,,
mondo:0024376,"sleep disorder, initiating and maintaining sleep",,,,,,,,,,,,,
mondo:0024377,"circadian rhythm sleep disorder, delayed sleep phase type","['DSPD', 'DSPS', 'delayed sleep phase syndrome']",0111141,,,C0393770,,,,,,G47.21,,
mondo:0024378,"circadian rhythm sleep disorder, advanced sleep phase type","['advanced sleep phase syndrome', 'ASPS']",,,,,,,,,327.32,G47.22,,
mondo:0024379,"circadian rhythm sleep disorder, irregular sleep wake type","['ISWD', 'irregular sleep-wake disorder']",,,,C0393771,,,,,327.33,G47.23,,
mondo:0024381,"circadian rhythm sleep disorder, jet lag type",['jet lag'],,,,C0231311,,,,,,G47.25,,
mondo:0024382,"circadian rhythm sleep disorder, shift work type",['shift work disorder'],,,,,,,,,,G47.26,,
mondo:0024386,"large cell lung carcinoma, clear cell variant","['clear cell carcinoma of the lung', 'clear cell carcinoma of lung, large cell type', 'large cell lung carcinoma, clear cell variant', 'clear cell lung carcinoma, large cell type', 'clear cell carcinoma of the lung, large cell type']",,,,C1707407,,C4451,,,,,,
mondo:0024387,benign ovarian sex cord-stromal tumor,"['ovarian sex cord-stromal tumor, benign', 'Sex cord stromal tumor, benign', 'benign Sex cord-stromal neoplasm of the ovary', 'benign Sex cord-stromal tumour of the ovary', 'benign ovarian Sex cord-stromal tumor', 'benign ovarian Sex cord-stromal tumour', 'benign Sex cord-stromal tumor of the ovary', 'benign ovarian Sex cord-stromal neoplasm', 'benign Sex cord-stromal tumour of ovary', 'benign Sex cord-stromal neoplasm of ovary', 'benign Sex cord-stromal tumor of ovary', 'ovarian SEX cord-stromal tumor, benign']",0080370,,,C1332528,,C6803,,,,,,
mondo:0024388,Clostridium infectious disease,"['infections, Clostridium', 'infection, Clostridium', 'Clostridium infection']",,,,,,,1000874,D003015,040.89,,,
mondo:0024389,anaerobic bacteria infectious disease,,,,,C0854328,,,,,041.84,,,
mondo:0024392,anaerobic balanitis,,,,,C0403764,,,,,,,,
mondo:0024410,infection caused by Bifidobacterium,['Bifidobacterium caused disease or disorder'],,,,C1096283,,,,,,,,
mondo:0024412,Peptostreptococcus infectious disease,['Peptostreptococcus caused disease or disorder'],,,,C1096562,,,,,041.84,,,
mondo:0024414,anaerobic cellulitis,,,,,C0241828,,,,,682.9,,,
mondo:0024415,hemorrhagic duodenitis,,,,,C0341245,,,,,535.61,,,
mondo:0024416,Neorickettsia infectious disease,['Neorickettsia caused disease or disorder'],,,,C0276121,,,,,,,,
mondo:0024417,perceptual disorders,,,,,,,,,D010468,,,,
mondo:0024418,muscular fibrosis multifocal obstructed vessels,,,,2033,,,,,,,,,
mondo:0024419,enthesitis,"['enthesis inflammation', 'enthesitis']",,,,C1282952,,C114470,,,,,,
mondo:0024421,short stature contractures hypotonia,['Hennekam Koss de Geest syndrome'],,,,,,,,,,,,
mondo:0024422,auditory perceptual disorders,"['processing disorder, auditory', 'acoustic perceptual disorder', 'disorder, auditory comprehension', 'disorder, acoustic perceptual', 'comprehension disorders, auditory', 'auditory processing disorder', 'perceptual disorders, acoustic', 'disorders, Psychoacoustical', 'auditory perceptual disorder', 'perceptual disorders, auditory', 'disorders, acoustic perceptual', 'auditory processing disorders', 'Psychoacoustical disorders', 'auditory comprehension disorder', 'auditory inattention', 'inattention, auditory', 'disorder, Psychoacoustical', 'perceptual disorder, acoustic', 'Inattentions, auditory', 'disorder, auditory processing', 'auditory comprehension disorders', 'acoustic perceptual disorders', 'auditory Inattentions', 'processing disorders, auditory', 'perceptual disorder, auditory', 'sensory perception of sound disease', 'disorders, auditory comprehension', 'disorder of sensory perception of sound', 'Psychoacoustical disorder', 'comprehension disorder, auditory', 'disorders, auditory processing']",,,,C0751257,,C84575,,D001308,,,,
mondo:0024429,Alice in Wonderland syndrome,,,,,,,C116362,,D062026,,,,
mondo:0024430,allesthesia,"['Alloesthesias', 'Allesthesias', 'Allachesthesia', 'Alloesthesia', 'Allachesthesias', 'false allochiria', 'Dyschirias', 'allochiria', 'dyschiria']",,,,,,,,D066190,,,,
mondo:0024431,bilirubin metabolism disease,,,,,,,,,,,,,
mondo:0024432,nerve plexus disorder,"['nerve plexus disease or disorder', 'nerve plexus disease', 'plexopathy', 'disease of nerve plexus', 'disorder of nerve plexus']",3688,,,C1335437,,C27744,,,,,,
mondo:0024454,sacral nerve plexus disorder,"['sacral nerve plexus disease or disorder', 'disorder of sacral nerve plexus', 'disease of sacral nerve plexus']",,,,C2931445,,,,C537224,,,,
mondo:0024455,autosomal dominant Robinow syndrome 1,"['DRS1', 'WNT5A autosomal dominant Robinow syndrome', 'Robinow dwarfism', 'dysostosis acral with facial and genital abnormalities', 'Robinow syndrome, autosomal dominant 1', 'autosomal dominant Robinow syndrome caused by mutation in WNT5A', 'acral dysostosis with Facial and genital abnormalities', 'fetal face syndrome', 'foetal face syndrome']",0060766,180700,,C0265205,,,,,,,,
mondo:0024456,anterior segment dysgenesis 3,"['ASGD3', 'iridogoniodysgenesis anomaly, autosomal dominant', 'iridogoniodysgenesis, type 1', 'IGDA', 'iridogoniodysgenesis type 1', 'IRID1', 'iridogoniodysgenesis caused by mutation in FOXC1', 'IGDA syndrome', 'glaucoma iridogoniodysplasia, familial', 'glaucoma iridogoniodysgenesia', 'iris hypoplasia with glaucoma', 'anterior segment dysgenesis 3', 'anterior segment dysgenesis 3, multiple subtypes', 'FOXC1 iridogoniodysgenesis']",0080608,601631,98978,C1839928,,,,C535535,,,,
mondo:0024457,neurodegeneration with brain iron accumulation 2A,"['neurodegeneration, Pla2g6-associated', 'neuroaxonal dystrophy, infantile', 'infantile neuroaxonal dystrophy', 'neurodegeneration with brain iron accumulation type 2A', 'Hunter Carpenter Macdonald syndrome', 'INAD1', 'Seitelberger disease', 'infantile neuroaxonal dystrophy/atypical neuroaxonal dystrophy', 'infantile neuroaxonal dystrophy 1', 'Hunter-Carpenter-McDonald syndrome', 'neurodegeneration with brain iron accumulation type 2a', 'inaD', 'PLAN', 'phospholipase A2-associated neurodegeneration', 'neurodegeneration with brain iron accumulation 2A', 'neurodegeneration, Pla2G6-associated', 'KARAK syndrome, included', 'NBIA2A', 'neuroaxonal dystrophy presenting with neonatal dysmorphic features, early onset of peripheral gangrene', 'neurodegeneration, PLA2G6-associated']",0110735,256600,35069,,"['0.1674', '0.3127', '0.1279', '-0.07837', '0.1798', '-0.7837', '-0.09393', '0.3235', '-0.4902', '-0.0758', '-0.08856', '-0.733', '-0.3542', '0.0741', '0.56', '-0.2634', '-0.0298', '-0.718', '-0.173', '-0.8286', '-0.1948', '-0.2837', '0.2228', '-0.2532', '-0.2197', '-0.325', '0.258', '-0.6123', '-0.544', '0.439', '0.533', '-0.1539', '0.1902', '-0.00921', '-0.371', '0.0869', '-0.4932', '-0.3035', '-0.263', '-0.05078', '0.6045', '-0.4636', '0.01608', '0.4934', '0.664', '0.1565', '-0.2086', '0.03036', '-0.771', '0.1', '0.2471', '0.5063', '-0.266', '-0.502', '0.2617', '-0.1396', '0.3574', '0.0618', '-0.568', '0.369', '0.08246', '-0.04407', '-0.003496', '-0.4006', '-0.1636', '-0.04175', '0.821', '0.2952', '0.07025', '0.4001', '-0.1544', '-0.05594', '0.0637', '-0.2998', '0.3696', '-0.2351', '-0.3267', '-0.4023', '-0.211', '0.03078', '0.3398', '-0.4963', '-0.05988', '0.8423', '0.3223', '0.373', '0.1522', '-0.0803', '0.91', '0.1324', '0.5854', '0.4507', '0.03745', '0.4438', '0.2603', '0.2861', '0.2605', '0.328', '-0.1252', '-0.048']",C84927,,C536071,330.8,,,
mondo:0024458,disorder of visual system,"['visual system disease', 'disorder of visual system', 'visual system disease or disorder', 'disease of visual system']",,,,,,,,,,,,
mondo:0024459,Aeromonas hydrophila intestinal disease,,,,,C2960005,,,,,008.47,,,
mondo:0024461,angiomatosis,"['multiple hemangiomas', 'angiomatosis', 'angiomatoses', 'diffuse angiomatosis', 'diffuse hemangioma']",,,,C0002992,,C27503,,D000798,,,,
mondo:0024462,familial cutaneous melanoma,['hereditary cutaneous melanoma (disease)'],,,,,,,,,,,,
mondo:0024463,ovarian dysgenesis 1,"['ovarian failure, hypergonadotropic', 'XX gonadal dysgenesis', 'gonadal dysgenesis, 20 type', 'XXGD', 'gonadal dysgenesis, XX type', 'ODG1', 'ovarian dysgenesis, hypergonadotropic, with normal karyotype', 'ovarian dysgenesis 1', 'ovarian dysgenesis, hypergonadotropic, autosomal recessive']",0080493,233300,,,,,,,,,,
mondo:0024464,"pituitary hormone deficiency, combined, 1","['combined pituitary hormone deficiencies, genetic form caused by mutation in POU1F1', 'POU1F1 combined pituitary hormone deficiencies, genetic form', 'pituitary hormone deficiency, combined, 1', 'pituitary hormone deficiency, combined or isolated, 1', 'CPHD1', 'pituitary hormone deficiency, combined 1']",,613038,,C2751608,,,,C567803,,,,
mondo:0024465,"surfactant metabolism dysfunction, pulmonary, 2","['desquamative interstitial pneumonitis due to surfactant Protein C deficiency', 'pulmonary alveolar proteinosis, congenital, 2', 'SMDP2', 'interstitial lung disease due to surfactant Protein C deficiency', 'surfactant metabolism dysfunction, pulmonary, 2']",,610913,440392,,"['-0.474', '0.1147', '-0.0779', '-0.03992', '0.11676', '-0.2335', '0.1396', '-0.0669', '-0.2822', '0.508', '-0.0565', '-0.077', '-0.1688', '-0.339', '-0.10754', '-0.3608', '-0.01941', '0.01712', '0.1171', '-0.701', '0.1087', '-0.399', '0.7573', '-0.2832', '-0.014336', '-0.1603', '0.07697', '0.4314', '0.07056', '-0.2229', '0.1556', '0.265', '0.558', '-0.02783', '0.002111', '-0.3806', '-0.4766', '0.2969', '0.0092', '-0.1525', '-0.1589', '-0.3042', '0.05978', '0.1722', '-0.3784', '0.2009', '-0.1333', '-0.1249', '0.1455', '0.2388', '0.0761', '0.2021', '0.1724', '0.04474', '-0.3362', '-0.3298', '-0.0673', '0.06586', '-0.2415', '-0.11206', '0.2343', '0.2195', '-0.2362', '-0.1938', '0.1129', '-0.3662', '0.785', '0.6313', '-0.2139', '0.1906', '-0.364', '0.0662', '0.1423', '0.2605', '-0.2559', '-0.178', '0.251', '0.002028', '-0.05252', '-0.3362', '-0.2612', '-0.082', '-0.3232', '0.00255', '-0.2944', '-0.08673', '0.235', '0.3992', '0.4211', '-0.1986', '0.3242', '0.4324', '-0.3008', '0.0877', '0.4385', '0.576', '0.2764', '-0.1174', '0.1661', '0.1464']",,,C567048,,,,
mondo:0024466,"facial paresis, hereditary congenital, 1","['Moebius syndrome 2', 'facial palsy, congenital, unilateral or bilateral', 'Moebius syndrome 2, formerly', 'facial paresis, hereditary congenital, 1', 'HCFP1', 'Mobius syndrome 2, formerly', 'Mobius syndrome 2']",,601471,,C1832284,,,,,,,,
mondo:0024467,apocrine sweat gland disorder,"['apocrine sweat gland disease', 'apocrine sweat gland disease or disorder', 'disorder of apocrine sweat gland', 'disease of apocrine sweat gland']",,,,,,,,,,L75,,
mondo:0024468,anterior pituitary gland disorder,"['adenohypophysis disease or disorder', 'adenohypophysis disease', 'disease of adenohypophysis', 'disorder of adenohypophysis']",,,,,,,,,253.9,,,
mondo:0024469,chondrogenic neoplasm,"['neoplasm of cartilage', 'tumour of the cartilage', 'tumor of cartilage', 'chondromatous tumor', 'chondromatous neoplasm', 'neoplasm of the cartilage', 'chondrogenic neoplasm', 'chondrogenic tumour', 'tumor of the cartilage', 'cartilaginous neoplasm', 'chondromatous tumour', 'cartilaginous tumor', 'cartilaginous tumour', 'chondrogenic tumor', 'tumour of cartilage']",,,,C0476147,,C4755,,,,,,
mondo:0024470,benign chondrogenic neoplasm,"['benign tumor of cartilage', 'benign tumour of cartilage', 'benign cartilaginous tumor', 'benign neoplasm of cartilage', 'benign chondrogenic tumor', 'benign chondrogenic neoplasm', 'benign tumour of the cartilage', 'chondrogenic neoplasm, benign', 'benign cartilaginous tumour', 'benign cartilaginous neoplasm', 'benign chondrogenic tumour', 'benign tumor of the cartilage', 'benign neoplasm of the cartilage']",,,,C0852519,,C8592,,,,,,
mondo:0024471,non-inflammatory vasculopathy,,,,496924,,,,,,,,,
mondo:0024472,boutonneuse fever,"['Kenya fever', 'Mediterranean tick fever', 'boutonneuse fever', 'African tick typhus', 'Mediterranean spotted fever', 'boutonneuse disease', 'fievre boutonneuse', 'marseilles fever', 'South African tick-bite fever', 'Rickettsia conorii spotted fever', 'Kenyan tick typhus', 'Kenya tick typhus', 'tick typhus due to rickettsia conorii', 'Conor and Bruch^s disease']",14095,,83313,C0006060,,,0007179,D001907,082.1,,10006045,
mondo:0024473,Astrakhan spotted fever,,0050041,,,,,,,,,,,
mondo:0024474,intraepithelial neoplasia,"['intraepithelial neoplasia', 'intraepithelial neoplasm', 'epithelial dysplasia']",,,,,,C8366,,,,,,
mondo:0024475,squamous cell intraepithelial neoplasia,"['sil', 'squamous cell intraepithelial neoplasia', 'SIN', 'squamous intraepithelial lesion']",,,,,,C8334,,,,,,
mondo:0024476,epithelial neoplasm of rectum,"['rectum epithelial neoplasm', 'rectal epithelial tumour']",,,,,,,,,,,,
mondo:0024477,liver and intrahepatic bile duct neoplasm,"['epithelial hepatic and intrahepatic bile duct neoplasm', 'tumor of liver', 'liver and intrahepatic bile duct epithelial neoplasm', 'liver tumour', 'tumour of liver', 'liver neoplasm', 'hepatic and intrahepatic bile duct neoplasm', 'liver neoplasm (disease)', 'neoplasm of liver', 'liver and intrahepatic bile duct neoplasm', 'liver tumor']",916,,,C1333976,,C7106,1001513,,,,,
mondo:0024478,mesenchymal hamartoma,['mesenchymal hamartoma'],,,,C0334090,,C40427,,,,,,
mondo:0024479,epithelial tumor of colon,['colon epithelial neoplasm'],,,,,,,,,,,,
mondo:0024480,dermatosis of eyelid,,,,,C1274150,,,,,,,,
mondo:0024481,skin appendage disorder,"['cutaneous appendage disease', 'cutaneous appendage disease or disorder', 'disorder of cutaneous appendage', 'disease of cutaneous appendage']",,,,C0037272,,,,,,L60-L75,,
mondo:0024482,eccrine sweat gland hamartoma,"['hamartoma of the eccrine sweat gland', 'eccrine sweat gland hamartoma', 'hamartoma of eccrine sweat gland', 'eccrine sweat gland hamartoma (disease)']",,,,C1333372,,C5564,,,,,,
mondo:0024483,urothelial hyperplasia,"['urothelium hyperplasia', 'urothelial hyperplasia']",,,,,,C27877,,,,,,
mondo:0024485,papillary urothelial hyperplasia,['papillary urothelial hyperplasia'],,,,,,C27879,,,,,,
mondo:0024487,nail infection,['nail infection'],,,,C0343026,,C78493,,,,,,
mondo:0024488,tumor grading characteristic,,,,,,,,,,,,,
mondo:0024489,general tumor grading characteristic,['disease grade qualifier'],,,,,,C28076,,,,,,
mondo:0024490,"tumor grade X, general grading system",,,,,,,,,,,,,
mondo:0024491,"tumor grade 1, general grading system","['grade 1', 'G1', 'grade I']",,,,C0475269,,C28077,,,,,,
mondo:0024492,"tumor grade 2, general grading system","['grade 2', 'G2', 'grade II']",,,,,,C28078,0005746,,,,,
mondo:0024493,"tumor grade 3, general grading system","['grade III', 'G3', 'grade 3']",,,,C0475271,,C28079,,,,,,
mondo:0024494,"tumor grade 4, general grading system","['grade IV', 'G4', 'grade 4']",,,,,,C28082,,,,,,
mondo:0024495,"tumor grade 1 or 2, general grading system",['grade 1/2'],,,,,,,,,,,,
mondo:0024496,"tumor grade 2 or 3, general grading system",['grade 2/3'],,,,,,C94678,,,,,,
mondo:0024497,"tumor grade 3 or 4, general grading system","['high grade', 'grade 3/4']",,,,,,C14158,,,,,,
mondo:0024498,glioma susceptibility 1,"['GLM1', 'glioblastoma, somatic', 'glioma susceptibility 1, autosomal dominant, somatic mutation', 'glioma, susceptibility to, somatic', 'subependymoma', 'glioma susceptibility 1', 'ependymoma', 'glioblastoma multiforme', 'glioma of brain, familial', 'oligodendroglioma', 'astrocytoma']",,137800,94,C1621958,,,,,,,,
mondo:0024499,vascular bone neoplasm,"['vascular bone neoplasm', 'bone vascular neoplasm', 'vascular tumor of bone', 'osseous vascular neoplasm', 'osseous vascular tumor', 'bone vascular tumor', 'osseous vascular tumour', 'bone vascular tumour', 'vascular neoplasm of the bone', 'vascular neoplasm of bone', 'vascular tumour of bone', 'vascular tumor of the bone', 'vascular tumour of the bone']",,,,C1336946,,C6478,,,,,,
mondo:0024500,duodenal neuroendocrine neoplasm,"['neuroendocrine neoplasm of duodenum', 'duodenum neuroendocrine tumor', 'duodenum NET', 'duodenum neuroendocrine tumour', 'duodenum neuroendocrine tumor, well differentiated, low or intermediate grade', 'duodenum neuroendocrine neoplasm']",,,,,,,,,,,,
mondo:0024501,appendix neuroendocrine neoplasm,"['neuroendocrine neoplasm of vermiform appendix', 'vermiform appendix neuroendocrine tumor', 'vermiform appendix neuroendocrine tumor, well differentiated, low or intermediate grade', 'vermiform appendix neuroendocrine tumour', 'appendix neuroendocrine neoplasm', 'vermiform appendix NET', 'vermiform appendix neuroendocrine neoplasm']",,,,,,C60709,,,,,,
mondo:0024502,gallbladder neuroendocrine neoplasm,"['gall bladder neuroendocrine tumor, well differentiated, low or intermediate grade', 'gall bladder NET', 'gall bladder neuroendocrine neoplasm', 'gallbladder neuroendocrine neoplasm', 'neuroendocrine neoplasm of gall bladder', 'gall bladder neuroendocrine tumor', 'gall bladder neuroendocrine tumour']",,,,C3273115,,C96917,,,,,,
mondo:0024503,digestive system neuroendocrine neoplasm,"['alimentary part of gastrointestinal system NET', 'gastro-enteropancreatic neuroendocrine tumor', 'gastroenteropancreatic endocrine tumor', 'GEP-NET', 'carcinoid tumour of digestive system', 'digestive system neuroendocrine tumor', 'neuroendocrine neoplasm of digestive system', 'carcinoid tumor', 'alimentary part of gastrointestinal system neuroendocrine tumor, well differentiated, low or intermediate grade', 'gastrointestinal neuroendocrine neoplasm', 'digestive system NET', 'GEP-NEN', 'GEP tumors', 'GEP tumours', 'digestive system neuroendocrine tumour', 'neuroendocrine neoplasm of alimentary part of gastrointestinal system', 'gastrointestinal system neuroendocrine neoplasm', 'carcinoid tumor of digestive system', 'carcinoid tumour', 'gastroenteropancreatic neuroendocrine neoplasm', 'digestive system neuroendocrine neoplasm', 'digestive system neuroendocrine tumor, well differentiated, low or intermediate grade', 'alimentary part of gastrointestinal system neuroendocrine tumor', 'alimentary part of gastrointestinal system neuroendocrine neoplasm', 'gastro-enteropancreatic neuroendocrine tumour', 'gastroenteropancreatic endocrine tumour', 'alimentary part of gastrointestinal system neuroendocrine tumour']",,,100092,CN197371,,C27721,,C535650,,,,
mondo:0024504,enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor,"['carcinoid tumour of pancreas', 'carcinoid tumor of the pancreas', 'serotonin-producing neuroendocrine tumor of pancreas', 'EC cell, serotonin producing pancreatic neuroendocrine tumour', 'serotonin-producing pancreatic neuroendocrine tumour', 'EC cell, serotonin producing pancreatic NET', 'pancreatic carcinoid tumor', 'EC cell, serotonin producing pancreatic neuroendocrine tumor', 'pancreatic serotonin producing tumor', 'serotonin-producing tumor of the pancreas', 'serotonin-producing tumour of the pancreas', 'serotonin-producing tumour of pancreas', 'pancreatic carcinoid tumour', 'enterochromaffin cell serotonin-producing pancreatic neuroendocrine tumor', 'carcinoid neoplasm of the pancreas', 'serotonin-producing PNET', 'carcinoid tumor of pancreas', 'pancreatic serotonin producing tumour', 'serotonin-producing pancreatic neuroendocrine tumor', 'serotonin-producing pancreatic NET', 'carcinoid tumour of the pancreas', 'pancreatic serotonin producing neoplasm', 'carcinoid neoplasm of pancreas', 'serotonin-producing tumor of pancreas', 'serotonin-producing neuroendocrine tumour of pancreas']",,,506090,,,C4446,,,,,,
mondo:0024506,Adams-Oliver syndrome 1,"['aplasia cutis congenita, congenital heart defect, and frontonasal cysts', 'Adams-Oliver syndrome 1', 'Adams-Oliver syndrome caused by mutation in ARHGAP31', 'AOS1', 'aplasia cutis congenita with terminal transverse limb defects', 'absence defect of limbs, scalp, and skull', 'ARHGAP31 Adams-Oliver syndrome', 'congenital scalp defects with distal limb reduction anomalies', 'AOS']",,100300,,CN028867,,,,,,,,
mondo:0024507,aniridia 1,"['aniridia', 'AN1', 'aniridia II', 'aniridia II, formerly', 'cataract, congenital, with late-onset corneal dystrophy', 'aniridia 1', 'cataract with late-onset corneal dystrophy']",,106210,,,,,,,,,,
mondo:0024508,"epilepsy, hot water, 1","['HWE1', 'epilepsy, hot water, 1', 'water immersion epilepsy', 'bathing epilepsy']",0081106,613339,,,,,,,,,,
mondo:0024512,"spondyloarthropathy, susceptibility to",['SPDA'],,,,CN118840,,,,,,,,
mondo:0024516,familial acne inversa,"['ACNINV', 'hereditary hidradenitis suppurativa', 'familial hidradenitis suppurativa']",,,,,,,,,,,,
mondo:0024517,schwannomatosis 1,"['schwannomatosis, somatic', 'schwannomatosis-1, susceptibility to', 'neurilemmomatosis, congenital cutaneous', 'SCHWANNOMATOSIS 1', 'SWNTS1']",,162091,,C4048809,,,,,,,,
mondo:0024518,reactive thrombocytosis,['secondary thrombocytosis'],,,,C0457506,,,,,286.9,,,
mondo:0024519,renal hypodysplasia/aplasia 1,"['renal adysplasia', 'hereditary renal aplasia', 'renal dysplasia, megalocystis, and sirenomelia', 'RHDA1', 'Selig Benacerraf Greene syndrome', 'renal aplasia', 'renal agenesis', 'renal hypodysplasia/aplasia 1']",,191830,,,"['0.003906', '0.01764', '-0.00908', '-0.01032', '0.004776', '-0.02672', '-0.0002359', '0.03317', '-0.02644', '-0.01454', '-0.01859', '0.001196', '0.0002842', '0.01065', '-0.01584', '-0.02628', '0.00821', '-0.007656', '-0.002787', '-0.03195', '0.001251', '-0.00105', '0.01678', '-0.003515', '0.003412', '-0.01761', '-0.0132', '-0.00913', '-0.011116', '-0.01143', '0.01993', '0.005085', '0.02238', '0.01042', '0.0076', '-0.0184', '-0.01125', '-0.00414', '-0.0063', '-0.00831', '0.003994', '-0.0222', '0.010826', '-9.46e-05', '-0.00885', '-0.02605', '-0.01755', '0.01234', '-0.0008335', '0.01808', '-0.00912', '-0.0095', '0.001475', '-0.00242', '-0.01301', '-0.01208', '0.02728', '-0.01572', '-0.03577', '-0.0004964', '0.01492', '0.01607', '0.00827', '-0.004208', '0.01076', '-0.000806', '0.01814', '0.025', '-0.01749', '0.01048', '-0.015015', '-0.006474', '0.003035', '-0.004913', '0.0137', '0.01642', '-0.00188', '-0.001586', '-0.00917', '-0.02576', '0.00522', '-6.366e-05', '-0.010445', '0.01423', '-0.00746', '-0.00379', '0.01909', '0.01523', '0.02649', '0.007614', '0.00676', '0.01863', '-0.00948', '-0.007378', '0.0482', '0.00574', '0.0313', '-0.03674', '-0.01153', '0.01144']",,,,,,,
mondo:0024520,renal hypodysplasia/aplasia 3,"['RHDA3', 'renal hypodysplasia/aplasia 3']",,617805,,CN703737,"['0.0068', '0.0707', '-0.001793', '0.01791', '0.0358', '-0.08514', '0.00514', '0.1292', '-0.07837', '-0.03513', '-0.02275', '-0.0301', '-0.007637', '0.02948', '-0.06586', '-0.05554', '-0.01788', '-0.05692', '-0.0007234', '-0.10706', '-0.02612', '-0.0373', '0.0678', '-0.03278', '0.04062', '-0.02438', '-0.01926', '0.01932', '-0.01466', '-0.0374', '0.09875', '-0.01793', '0.08887', '0.02429', '-0.00454', '-0.08234', '-0.0328', '-0.04376', '-0.01117', '-0.0349', '0.0361', '-0.07605', '0.0526', '-0.03363', '-0.0169', '-0.06094', '-0.0394', '0.0397', '-0.01738', '0.01221', '-0.04984', '-0.02454', '0.00946', '-0.01005', '-0.05795', '-0.02205', '0.0587', '-0.0414', '-0.1378', '0.0009236', '0.0832', '0.03088', '-0.007328', '0.003754', '0.02774', '-0.011215', '0.0908', '0.07513', '-0.06012', '0.06104', '-0.0449', '0.0008435', '0.0353', '-0.0593', '0.0627', '0.0491', '0.0144', '0.0007834', '-0.0805', '-0.0508', '-0.006172', '0.011154', '-0.004395', '0.0456', '-0.02649', '-0.003073', '0.03336', '0.07227', '0.0898', '0.01613', '0.03763', '0.07263', '-0.03442', '-0.02339', '0.1409', '0.03873', '0.0884', '-0.086', '-0.02538', '0.04138']",,0009137,,,,,
mondo:0024521,"aortic aneurysm, familial abdominal, 1","['aortic aneurysm, familial abdominal 1', 'abdominal aortic aneurysm', 'aneurysm, abdominal aortic', 'aortic aneurysm, familial abdominal, 1', 'AAA1']",,100070,,,,,,,,,,
mondo:0024522,"amyloidosis, primary localized cutaneous, 1","['lichen amyloidosis, familial', 'PCA', 'amyloidosis, primary localized cutaneous, 1', 'amyloidosis, primary localized cutaneous, type 1', 'amyloidosis 9', 'OSMR primary cutaneous amyloidosis', 'amyloidosis, primary cutaneous, 1', 'amyloidosis, familial cutaneous lichen', 'amyloidosis, primary localised cutaneous, type 1', 'primary cutaneous amyloidosis caused by mutation in OSMR', 'PLCA1']",0080930,105250,,C0268398,,,,,,,,
mondo:0024523,aortic valve disease 1,"['bicuspid aortic valve', 'aortic valve, calcification of', 'NOTCH1 aortic valve disease', 'aortic valve disease', 'aortic valve disease caused by mutation in Notch1', 'aortic valve, bicuspid', 'Notch1 aortic valve disease', 'aortic stenosis, calcific', 'AOVD1', 'aortic valve disease 1']",0080333,109730,,C3887892,,,,,,,,
mondo:0024524,dyschromatosis universalis hereditaria 1,"['dyschromatosis universalis hereditaria 1', 'DUH1']",,127500,,C2675711,,,,C567273,,,,
mondo:0024525,Fanconi renotubular syndrome 1,"['Fanconi renotubular syndrome 1', 'Fanconi renotubular syndrome', 'renal Fanconi syndrome', 'adult Fanconi syndrome', 'primary Fanconi renal syndrome', 'DeToni-Debré-Fanconi syndrome', 'Luder-Sheldon syndrome', 'FRTS1', 'primary Fanconi renotubular syndrome', 'Fanconi syndrome without cystinosis']",0080757,134600,3337,,"['-0.12463', '0.1702', '0.1564', '0.05893', '0.1029', '-0.0445', '-0.1499', '0.1428', '0.00166', '-0.010765', '-0.03525', '-0.10284', '-0.0766', '0.1683', '-0.2654', '-0.2316', '0.01588', '0.1392', '-0.0388', '-0.252', '0.05804', '-0.0833', '0.1476', '-0.0569', '0.2166', '-0.1777', '0.0284', '0.06396', '-0.10535', '-0.0604', '0.1519', '-0.0758', '0.05725', '0.08734', '-0.0488', '-0.1201', '-0.1287', '0.1877', '-0.04196', '-0.332', '-0.0657', '-0.1375', '0.11426', '-0.2272', '-0.1967', '-0.5034', '0.2015', '0.0331', '0.1857', '0.2705', '-0.194', '-0.08484', '0.1898', '-0.134', '-0.02965', '-0.2069', '0.2306', '-0.04645', '-0.2966', '-0.02458', '0.1898', '0.03583', '-0.004395', '-0.09204', '0.043', '0.02571', '0.2418', '0.0764', '-0.2551', '0.01602', '-0.08057', '0.1041', '-0.04306', '-0.0741', '-0.12024', '0.1936', '0.03613', '0.054', '-0.04886', '0.04843', '-0.02061', '-0.01645', '-0.02437', '0.08936', '-0.02324', '0.0187', '-0.010155', '-0.1514', '0.3364', '-0.05115', '0.01263', '0.1758', '-0.1765', '-0.02145', '0.2905', '0.2395', '0.003536', '-0.2148', '-0.2107', '0.3562']",,,,,,,
mondo:0024526,Zimmermann-Laband syndrome 1,"['ZLS1', 'KCNH1 Zimmermann-Laband syndrome', 'Laband syndrome', 'Zimmermann-Laband syndrome 1', 'fibromatosis, gingival, with abnormal fingers, fingernails, Nose, and ears, and splenomegaly', 'Zimmermann-Laband syndrome caused by mutation in KCNH1']",,135500,,CN032818,,,,,,,,
mondo:0024527,glomerulopathy with fibronectin deposits 1,"['lobular glomerulopathy, familial', 'glomerulopathy with fibronectin deposits 1', 'GFND1', 'glomerulopathy with giant fibrillar deposits']",,137950,,,,,,,,,,
mondo:0024528,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1","['progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1', 'autosomal dominant progressive external ophthalmoplegia caused by mutation in POLG', 'progressive external ophthalmoplegia, autosomal dominant 1', 'POLG autosomal dominant progressive external ophthalmoplegia', 'PEOA1']",0111521,157640,,C1834846,,,,,,,,
mondo:0024529,MVP1,"['mitral regurgitation, familial', 'PMV', 'MVP1', 'mitral valve prolapse 1', 'mitral valve prolapse, familial', 'mitral valve prolapse, familial, X-linked', 'mitral valve prolapse, myxomatous 1', 'myxomatous valvular disease, familial', 'click-murmur syndrome', 'floppy mitral valve', 'prolapsed mitral valve', 'myxomatous mitral valve prolapse 1', 'barlow syndrome']",,157700,,CN074267,,,,,,,,
mondo:0024530,Bethlem myopathy 1,"['myopathy, benign congenital, with contractures', 'muscular dystrophy, benign congenital', 'Bethlem myopathy 1', 'Bethlem myopathy', 'BTHLM1']",,158810,,CN029274,,,,,,,,
mondo:0024531,"myopathy, tubular aggregate, 1","['tubular aggregate myopathy', 'tubular aggregate myopathy caused by mutation in STIM1', 'myopathy, tubular aggregate', 'TAM1', 'STIM1 tubular aggregate myopathy', 'myopathy, tubular aggregate, 1']",,160565,,C4011726,,,,,,,,
mondo:0024532,otofaciocervical syndrome 1,"['EYA1 otofaciocervical syndrome', 'OFC', 'otofaciocervical syndrome', 'otofaciocervical syndrome caused by mutation in EYA1', 'otofaciocervical syndrome 1', 'OTFCS', 'OFC1']",,166780,,CN034490,,,,,,,,
mondo:0024533,"pulmonary hypertension, primary, 1","['pulmonary hypertension, primary, Fenfluramine-associated', 'PHT', 'pulmonary arterial hypertension', 'BMPR2 primary pulmonary hypertension', 'pulmonary hypertension, primary, fenfluramine or dexfenfluramine-associated', 'pulmonary hypertension, primary, Dexfenfluramine-associated', 'pulmonary hypertension, primary, 1, with hereditary hemorrhagic telangiectasia', 'primary pulmonary hypertension caused by mutation in BMPR2', 'pulmonary hypertension, familial primary, 1, with or without HHT', 'PPH1', 'pulmonary hypertension, primary, 1', 'Pph1 with Hht']",,178600,,C3203102,,,,,,,,
mondo:0024534,Dowling-Degos disease 1,"['KRT5 Dowling-Degos disease', 'reticular pigment anomaly of flexures', 'DDD1', 'DDD', 'Dowling-Degos disease caused by mutation in KRT5', 'Dowling-Degos disease 1']",,179850,,C3714534,,,,,,,,
mondo:0024535,Singleton-Merten syndrome 1,"['SGMRT1', 'singleton-Merten dysplasia caused by mutation in IFIH1', 'IFIH1 singleton-Merten dysplasia', 'singleton-Merten syndrome 1']",,182250,,C4225427,,,,,,,,
mondo:0024536,glucocorticoid deficiency 1,"['adrenal unresponsiveness to ACTH', 'MC2R familial glucocorticoid deficiency', 'GCCD1', 'ACTH resistance', 'glucocorticoid deficiency, due to ACTH unresponsiveness', 'familial glucocorticoid deficiency caused by mutation in MC2R', 'familial glucocorticoid deficiency 1', 'glucocorticoid deficiency 1']",0080621,202200,,C1859974,,,,,,,,
mondo:0024537,Brown-Vialetto-van Laere syndrome 1,"['Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A3', 'SLC52A3 Brown-Vialetto-van Laere syndrome', 'bulbar palsy, progressive, with sensorineural deafness', 'Brown-Vialetto-Van Laere syndrome 1', 'pontobulbar palsy with deafness', 'RTD2', 'Riboflavin transporter deficiency 2', 'BVVLS1', 'rfvt2-related riboflavin transporter deficiency']",0080785,211530,572543,CN029849,"['-0.03137', '0.0903', '0.004276', '-0.01453', '0.02638', '-0.0996', '0.014084', '0.0649', '-0.0707', '-0.02725', '-0.01455', '-0.02246', '0.002476', '-0.01253', '-0.01938', '-0.05118', '-0.006905', '-0.02307', '-0.01974', '-0.1301', '-0.0203', '-0.03384', '0.0773', '-0.03256', '0.02293', '-0.02762', '-0.03375', '-0.03528', '0.02704', '-0.06274', '0.0719', '-0.02463', '0.08875', '0.0483', '0.01392', '-0.0519', '-0.02531', '-0.02127', '-0.01041', '-0.0667', '0.02617', '-0.0926', '0.0377', '-0.04578', '-0.01214', '-0.0852', '-0.01656', '0.07025', '0.03198', '0.01581', '-0.01881', '-0.0377', '0.002392', '-0.00599', '-0.0493', '-0.02306', '0.078', '-0.04077', '-0.10504', '0.0282', '0.06003', '0.04584', '0.01115', '0.031', '0.02167', '-0.0002508', '0.0826', '0.03772', '-0.0866', '0.1077', '-0.07544', '-0.006466', '0.02481', '-0.0621', '0.03198', '0.03986', '-0.01428', '0.009384', '-0.0792', '-0.0496', '0.02278', '0.00835', '-0.04987', '0.0627', '-0.03705', '-0.0142', '0.03998', '0.1211', '0.0957', '0.00513', '0.03096', '0.0541', '0.01118', '0.008934', '0.1588', '0.03983', '0.08563', '-0.1558', '-0.01633', '0.02652']",C133724,,,,,,
mondo:0024538,"basal ganglia calcification, idiopathic, 1","['IBGC1', 'basal ganglia calcification, idiopathic, 3, formerly', 'striopallidodentate calcinosis, bilateral', 'basal ganglia calcification, idiopathic, 3', 'basal ganglia calcification, idiopathic, 2', 'idiopathic basal ganglia calcification 1', 'basal ganglia calcification, idiopathic, type 1', 'IBGC2', 'ferrocalcinosis, cerebrovascular', 'Fahr disease, familial, formerly', 'cerebral calcification, nonarteriosclerotic, idiopathic, adult-onset', 'Fahr disease, familial', 'striopallidodentate calcinosis, autosomal dominant, adult-onset', 'basal ganglia calcification, idiopathic, 1']",,606656,,C1847731,,C129973,,C537657,,,,
mondo:0024539,"choroidal dystrophy, central areolar, 1","['choroidal dystrophy, central areolar', 'choroidal sclerosis', 'choroidal dystrophy, central areolar 1', 'choroidal dystrophy, central areolar, 1', 'CACD1', 'central areolar choroidal dystrophy caused by mutation in GUCY2D', 'GUCY2D central areolar choroidal dystrophy']",,215500,,,,,,,,,,
mondo:0024540,Jervell and Lange-Nielsen syndrome 1,"['KCNQ1 Jervell and Lange-Nielsen syndrome', 'Jervell and Lange-Nielsen syndrome', 'deafness, congenital, and functional heart disease', 'Surdo-Cardiac syndrome', 'JLNS1', 'Jervell and Lange-Nielsen syndrome 1', 'prolonged QT interval in Ekg and sudden death', 'Jervell and Lange-Nielsen syndrome caused by mutation in KCNQ1', 'Cardioauditory syndrome of Jervell and Lange-Nielsen']",,220400,,CN034131,,,,,,,,
mondo:0024541,trichohepatoenteric syndrome 1,"['tricho-hepato-enteric syndrome caused by mutation in TTC37', 'THES1', 'The syndrome', 'diarrhea, fatal infantile, with trichorrhexis nodosa', 'TTC37 tricho-hepato-enteric syndrome', 'TRICHOHEPATOENTERIC syndrome 1', 'diarrhea, syndromic']",0111415,222470,,CN034858,,,,,,,,
mondo:0024542,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1","['cerebellar hypoplasia and mental retardation with or without quadrupedal locomotion 1', 'cerebellar ataxia, congenital, and mental retardation, autosomal recessive', 'cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 1', 'cerebellar hypoplasia, VLDLR-associated', 'dysequilibrium syndrome', 'cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 1', 'cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 1', 'VLDLR dysequilibrium syndrome', 'cerebellar ataxia and mental retardation with or without quadrupedal locomotion 1', 'cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 1', 'cerebellar ataxia, mental retardation, and dysequilibrium syndrome 1', 'dysequilibrium syndrome caused by mutation in VLDLR', 'cerebellar ataxia, congenital, and intellectual disability, autosomal recessive', 'CAMRQ1']",,224050,,CN074243,,,,,,,,
mondo:0024543,brittle cornea syndrome 1,"['brittle cornea syndrome caused by mutation in ZNF469', 'ZNF469 brittle cornea syndrome', 'BCS1', 'brittle cornea syndrome 1', 'corneal fragility, keratoglobus, blue sclerae, Joint hyperextensibility', 'Fragilitas oculi with Joint hyperextensibility', 'dysgenesis Mesodermalis corneae Et sclerae', 'Ehlers-Danlos syndrome, type Vib', 'Ehlers-Danlos syndrome, type Vib, formerly']",,229200,,,,,,C536192,,,,
mondo:0024545,Miyoshi muscular dystrophy 1,"['MMD1', 'muscular dystrophy, distal, late-onset, autosomal recessive', 'Miyoshi myopathy caused by mutation in DYSF', 'DYSF Miyoshi myopathy', 'MIYOSHI muscular dystrophy 1', 'Miyoshi myopathy']",0070199,254130,,C1850808,,,,,,,,
mondo:0024546,"hypertrophic osteoarthropathy, primary, autosomal recessive, 1","['PDP, autosomal recessive', 'hypertrophic osteoarthropathy, primary, autosomal recessive 1', 'Currarino idiopathic osteoarthropathy', 'Cranioosteoarthropathy', 'hypertrophic osteoarthropathy, primary, autosomal recessive, 1', 'familial idiopathic osteoarthropathy of childhood', 'primary hypertrophic osteoarthropathy caused by mutation in HPGD', 'Touraine-Solente-Gole syndrome', 'Pho, autosomal recessive', 'pachydermoperiostosis, autosomal recessive', 'PHOAR1', 'HPGD primary hypertrophic osteoarthropathy']",,259100,1525,,"['-0.2448', '-0.2715', '0.5513', '-0.1918', '0.771', '-0.274', '-0.19', '0.791', '-0.4768', '0.161', '-0.4849', '-0.132', '-0.385', '-0.411', '-0.04315', '-0.2079', '0.408', '-0.225', '-0.445', '-1.069', '0.2168', '-0.06396', '0.4663', '-0.8564', '0.3777', '0.5825', '-0.004196', '0.0423', '0.4993', '-0.2136', '0.302', '-0.04025', '-0.12054', '-0.4014', '0.1145', '-0.5054', '-0.2913', '-0.3948', '0.1212', '-0.538', '-0.04724', '-0.32', '0.5767', '-0.05698', '0.1135', '-0.2874', '0.3396', '0.3933', '0.07654', '0.3022', '0.2888', '-0.1674', '0.1788', '0.316', '-0.573', '-0.8926', '0.2468', '0.4714', '-0.06604', '-0.1136', '0.4534', '0.4236', '0.11993', '-0.3835', '0.1884', '-0.2351', '0.1855', '1.025', '-0.2081', '0.03638', '-0.5454', '0.013725', '0.356', '-0.377', '0.1929', '0.492', '-0.4563', '-0.1159', '-0.2737', '-0.02478', '0.328', '0.3325', '0.1001', '0.1425', '0.1096', '-0.1605', '0.2485', '0.1032', '-0.1327', '-0.03137', '-0.4338', '-0.1606', '-0.01411', '0.5103', '0.597', '0.7847', '0.7305', '-0.2378', '0.6006', '-0.699']",,,,,,,
mondo:0024547,pancreatic agenesis 1,"['pancreatic agenesis 1', 'PAGEN1', 'Pagen', 'pancreatic hypoplasia, congenital', 'pancreatic agenesis caused by mutation in PDX1', 'PDX1 pancreatic agenesis']",,260370,,C3891828,,,,,,,,
mondo:0024548,peeling skin syndrome 1,"['CDSN peeling skin syndrome', 'skin peeling, familial continuous generalized', 'PSS type B', 'peeling skin syndrome type B', 'PSS', 'peeling skin syndrome caused by mutation in CDSN', 'deciduous skin', 'inflammatory peeling skin syndrome', 'generalized peeling skin syndrome type B', 'PSS1', 'peeling skin syndrome 1', 'generalized deciduous skin type B', 'generalised peeling skin syndrome type B', 'generalised deciduous skin type B', 'skin peeling, familial continuous generalised', 'keratolysis exfoliativa congenita']",,270300,263553,CN202306,"['0.3613', '-0.5605', '-0.5576', '-0.3171', '0.0564', '-0.2764', '-0.1517', '0.07306', '0.03314', '-0.2079', '-0.11206', '0.0845', '-0.288', '0.03912', '-0.283', '0.4773', '0.1338', '0.0666', '-0.2007', '-0.8267', '-0.2006', '-0.1752', '0.5356', '-0.3914', '0.1522', '-0.05402', '-0.38', '0.10944', '-0.1761', '-0.2098', '0.368', '-0.1434', '0.0498', '0.3225', '-0.1732', '0.04684', '-0.8467', '-0.7173', '0.01912', '0.2075', '0.144', '-0.8457', '0.1705', '-0.1805', '-0.2499', '0.234', '-0.2878', '0.1136', '0.322', '-0.0483', '-0.2219', '-0.651', '0.5703', '0.11255', '-0.5747', '0.5474', '-0.0464', '-0.2329', '-0.476', '-0.4148', '-0.2751', '0.506', '-0.337', '-0.3633', '0.2057', '0.4033', '0.4897', '0.4312', '-0.05212', '0.883', '-0.5093', '-0.5596', '-0.2576', '-0.1609', '-0.02773', '0.1884', '-0.2446', '-0.649', '0.2034', '-0.3586', '0.09406', '-0.457', '-0.1023', '-0.2554', '-0.2036', '-0.154', '-0.2076', '0.509', '0.544', '0.3958', '0.385', '0.326', '0.547', '0.5728', '0.4067', '0.413', '0.0686', '-0.4175', '0.0674', '-0.2153']",,,,,,,
mondo:0024549,microphthalmia with coloboma 1,"['microphthalmia, isolated, with coloboma 1', 'microphthalmia, colobomatous, isolated 1', 'MCOPCB1']",,300345,,,,,,,,,,
mondo:0024550,frontometaphyseal dysplasia 1,"['FLNA frontometaphyseal dysplasia', 'FRONTOMETAPHYSEAL dysplasia 1', 'Fmd', 'frontometaphyseal dysplasia 1, X-linked recessive', 'FMD1', 'frontometaphyseal dysplasia caused by mutation in FLNA']",0111786,305620,,,,,,,,,,
mondo:0024551,X-linked lymphoproliferative disease due to SH2D1A deficiency,"['Xlp', 'infectious mononucleosis, Severe, susceptibility to', 'lymphoproliferative disease, X-linked', 'Epstein-Barr Virus infection, familial fatal', 'immunodeficiency 5', 'Purtilo syndrome', 'EBV infection, Severe, susceptibility to', 'XLP1', 'Duncan disease', 'lymphoproliferative syndrome, X-linked, 1', 'Lyp', 'immunodeficiency, X-linked progressive combined variable', 'lymphoproliferative syndrome, X-linked, 1, X-linked recessive']",,308240,538931,,,,,,,,,
mondo:0024552,linear skin defects with multiple congenital anomalies 1,"['microphthalmia, dermal aplasia, and sclerocornea', 'Midas syndrome', 'linear skin defects with multiple congenital anomalies 1', 'HCCS microphthalmia with linear skin defects syndrome', 'LSDMCA1', 'microphthalmia with linear skin defects', 'linear skin defects with multiple congenital anomalies 1, X-linked dominant', 'microphthalmia, syndromic 7', 'microphthalmia with linear skin defects syndrome caused by mutation in HCCS']",0111808,309801,,,,,,,,,,
mondo:0024553,"myopathy, lactic acidosis, and sideroblastic anemia 1","['mitochondrial myopathy and sideroblastic anemia', 'myopathy, lactic acidosis, and sideroblastic anemia 1', 'mitochondrial myopathy and sideroblastic anaemia', 'PUS1 myopathy, lactic acidosis, and sideroblastic anaemia', 'myopathy, lactic acidosis, and sideroblastic anaemia caused by mutation in PUS1', 'myopathy, lactic acidosis, and sideroblastic anemia caused by mutation in PUS1', 'MLASA1', 'PUS1 myopathy, lactic acidosis, and sideroblastic anemia']",0111185,600462,,C1838103,,,,,,,,
mondo:0024554,D-2-hydroxyglutaric aciduria 1,"['D-2-hydroxyglutaric aciduria caused by mutation in D2HGDH', 'D-2-hydroxyglutaric aciduria 1', 'D2HGDH D-2-hydroxyglutaric aciduria', 'D-2-hydroxyglutaric aciduria', 'D2HGA1']",0111351,600721,,C3152055,,,,,,,,
mondo:0024555,megalencephalic leukoencephalopathy with subcortical cysts 1,"['VL', 'leukoencephalopathy with swelling and cysts', 'megalencephalic leukoencephalopathy with subcortical cysts 1', 'megalencephalic leukoencephalopathy with subcortical cysts', 'Van Der Knaap disease', 'MLC1', 'Vacuolating megalencephalic leukoencephalopathy with subcortical cysts', 'Lvm']",0080316,604004,,,,,,,,,,
mondo:0024556,"epilepsy, familial focal, with variable foci 1","['epilepsy, partial, with variable foci', 'DEPDC5 epilepsy, familial focal, with variable foci', 'epilepsy, familial focal, with variable foci caused by mutation in DEPDC5', 'epilepsy, familial focal, with variable foci 1', 'epilepsy, familial focal, with variable foci', 'FFEVF1']",,604364,,C1858477,,C161005,,,,,,
mondo:0024557,ataxia-telangiectasia-like disorder 1,"['ataxia-telangiectasia-like disorder 1', 'MRE11 ataxia - telangiectasia-like disorder', 'ataxia-telangiectasia-like disorder caused by mutation in MRE11', 'MRE11 ataxia-telangiectasia-like disorder', 'Atld', 'ATLD1']",,604391,251347,C1858391,"['-0.1348', '-0.411', '0.1032', '0.0649', '-0.2408', '-1.13', '0.2673', '8.58e-05', '-0.6323', '-0.897', '0.2499', '0.2386', '-0.2927', '0.1543', '0.4634', '-0.3013', '-0.214', '-0.2054', '0.0006194', '-1.098', '-0.06476', '-0.4084', '0.305', '-0.6323', '0.5537', '-0.5728', '-0.3423', '0.2405', '-0.08185', '-0.7803', '-0.02516', '0.4644', '-0.624', '-0.12103', '0.4316', '0.1227', '-0.2761', '0.10205', '0.4873', '0.2764', '0.2893', '0.376', '-0.389', '0.601', '0.6533', '-0.7935', '0.3076', '0.4307', '0.645', '0.04523', '-0.1973', '0.2242', '-0.1888', '-0.2869', '-0.03372', '-0.7817', '0.5166', '0.5205', '-0.1422', '0.562', '-0.6855', '0.2401', '0.3071', '-0.1588', '-0.4932', '0.562', '0.3967', '0.6367', '-0.585', '0.3093', '0.897', '0.4175', '-0.10406', '-0.6704', '0.7886', '0.3386', '0.2922', '0.501', '0.1984', '0.5107', '-0.4067', '-0.8154', '0.3938', '0.8535', '-0.2205', '-0.7', '0.305', '0.1359', '0.4724', '0.5347', '0.2727', '0.5303', '0.0545', '-0.0078', '1.061', '1.047', '0.473', '0.2178', '-0.436', '-0.04224']",C132224,,,,,,
mondo:0024558,radioulnar synostosis with amegakaryocytic thrombocytopenia 1,"['HOXA11 radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome', 'radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome caused by mutation in HOXA11', 'radioulnar synostosis with amegakaryocytic thrombocytopenia 1', 'thrombocytopenia, congenital, with radioulnar synostosis', 'RUSAT1', 'Rusat']",,605432,,,,,,,,,,
mondo:0024559,"aortic aneurysm, familial thoracic 1","['aortic dissection, familial', 'AAT1', 'aneurysm, thoracic aortic', 'FAA1', 'Erdheim cystic medial necrosis of aorta', 'aortic aneurysm, familial thoracic', 'annuloaortic ectasia']",,607086,229,,,,,C562834,,,,
mondo:0024560,PDA1,"['patent ductus arteriosus 1', 'PDA1', 'patent ductus arteriosus, susceptibility to', 'PDA']",,607411,,,,,,,,,,
mondo:0024561,vitelliform macular dystrophy 3,"['foveomacular dystrophy, adult-onset', 'PRPH2 vitelliform macular dystrophy', 'macular dystrophy, vitelliform, 3', 'VMD3', 'vitelliform macular dystrophy, adult-onset', 'vitelliform macular dystrophy caused by mutation in PRPH2', 'foveomacular dystrophy, adult-onset, with or without choroidal neovascularization']",,608161,,,,,,,,,,
mondo:0024562,sick sinus syndrome 1,"['sinus rhythm, congenital absence of', 'sick sinus syndrome caused by mutation in SCN5A', 'sinus node disease, familial, autosomal recessive', 'sick sinus syndrome, congenital', 'sick sinus syndrome 1', 'sinus bradycardia syndrome, familial', 'SSS1', 'SCN5A sick sinus syndrome']",,608567,,,,,,,,,,
mondo:0024563,"herpes simplex encephalitis, susceptibility to, 1","['encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 1', 'herpes simplex encephalitis, susceptibility to, 1', 'encephalopathy, acute, infection-induced, susceptibility to, 1', 'encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 1', 'UNC93B1 herpes simplex encephalitis', 'IIAE1', 'herpes simplex encephalitis caused by mutation in UNC93B1']",,610551,,,,,,,,,,
mondo:0024564,cerebroretinal microangiopathy with calcifications and cysts 1,"['Coats plus syndrome caused by mutation in CTC1', 'CTC1 Coats plus syndrome', 'Coats plus syndrome', 'CRMCC1', 'cerebroretinal microangiopathy with calcifications and cysts 1', 'Crmcc', 'cerebroretinal microangiopathy with calcifications and cysts']",,612199,,,,,,,,,,
mondo:0024565,ectodermal dysplasia-syndactyly syndrome 1,"['ectodermal dysplasia-syndactyly syndrome caused by mutation in NECTIN4', 'NECTIN4 ectodermal dysplasia-syndactyly syndrome', 'EDSS1', 'ectodermal dysplasia-syndactyly syndrome 1']",,613573,,C3150807,,,,,,,,
mondo:0024566,"febrile seizures, familial, 11","['FEB11', 'febrile seizures, familial, 11', 'convulsions, familial febrile, 11']",0111308,614418,,C3280734,,,,,,,,
mondo:0024567,"hypotonia, infantile, with psychomotor retardation and characteristic facies 1","['hypotonia, infantile, with psychomotor retardation and characteristic facies 1', 'Ihprf', 'NALCN hypotonia, infantile, with psychomotor retardation and characteristic facies', 'hypotonia, infantile, with psychomotor retardation and characteristic facies caused by mutation in NALCN', 'IHPRF1']",,615419,,C3809454,,,,,,,,
mondo:0024568,infantile liver failure syndrome 1,"['LARS infantile liver failure', 'infantile liver failure caused by mutation in Lars', 'Lars infantile liver failure', 'infantile liver failure syndrome 1', 'infantile liver failure syndrome type 1', 'ILFS1']",0080717,615438,370088,C3809522,,,,,,,,
mondo:0024569,optic atrophy 8,"['OPA8', 'optic atrophy 8']",0111439,616648,,C4085249,,,,,,,,
mondo:0024570,hyperparathyroidism 4,"['GCM2 familial isolated hyperparathyroidism', 'HRPT4', 'familial isolated hyperparathyroidism caused by mutation in GCM2', 'hyperparathyroidism type 4', 'hyperparathyroidism 4']",,617343,,CN240514,,,,,,,,
mondo:0024571,AIDS-related disorder,"['AIDS-related complications', 'disease associated with AIDS', 'AIDS-related disorder', 'AIDS/HIV - relatedDisease associated with AIDS']",,,,C0877121,,C4991,,,,,,
mondo:0024572,immunodeficiency-related disorder,"['Immunosuppression disorders', 'Immunosuppression-related disorder', 'Immunodepression-related disorder', 'immunodeficiency-related disorder']",,,,C1334159,,C35686,,,,,,
mondo:0024573,familial hypertrophic cardiomyopathy,"['hereditary hypertrophic cardiomyopathy', 'cardiomyopathy, familial hypertrophic', 'hypertrophic familial cardiomyopathy', 'familial hypertrophic cardiomyopathy', 'familila or idiopathic hypertrophic obstructive cardiomyopathy']",0080326,,155,,"['-0.01229', '0.03433', '-0.00995', '-0.00906', '0.01165', '-0.0471', '0.0174', '0.0414', '-0.02652', '0.007072', '-0.004707', '-0.0247', '-0.0073', '-0.00178', '-0.01677', '-0.0354', '-0.01433', '-0.01369', '-0.01002', '-0.0657', '0.001147', '-0.006054', '0.02347', '-0.0002718', '0.013214', '-0.0018635', '0.004704', '0.00814', '0.0109', '-0.01927', '0.03098', '-0.01224', '0.03632', '0.01027', '0.00911', '-0.014465', '-0.01854', '-0.01166', '0.003649', '-0.026', '0.00757', '-0.02211', '0.02118', '0.00772', '0.002262', '-0.005863', '-0.01265', '0.02777', '-0.001766', '0.00534', '-0.007484', '-0.001957', '0.00712', '0.004627', '-0.011215', '-0.01894', '0.015366', '-0.005085', '-0.03214', '-0.002483', '0.00844', '0.007744', '0.01642', '0.002222', '-0.01073', '0.01109', '0.0311', '0.02855', '-0.0236', '0.04248', '-0.02803', '-0.002403', '0.01585', '-0.00974', '0.01075', '0.007355', '-0.00485', '-0.014435', '-0.01261', '-0.0157', '0.00987', '-0.00279', '-0.00659', '-0.006264', '-0.003653', '0.007202', '0.02167', '0.01778', '0.0327', '0.01446', '0.01077', '0.01405', '-0.01088', '0.02345', '0.05276', '0.02122', '0.03036', '-0.03925', '-0.01434', '0.01047']",C84773,,D024741,,,,
mondo:0024574,von Willebrand disease (hereditary or acquired),"['VWD', 'von Willebrand^s disease', 'von Willebrand disorder']",,,,,,C68677,,D014842,286.4,D68.0,,
mondo:0024575,pregnancy disorder,"['complication, pregnancy', 'pregnancy complication', 'disorder of pregnancy', 'Complications, pregnancy', 'pregnancy disorder']",,,,,,C35169,,D011248,,,,
mondo:0024582,male reproductive system neoplasm,"['tumour of male reproductive organ', 'neoplasm of the Male reproductive system', 'tumor of the Male reproductive system', 'tumor of male reproductive organ', 'male reproductive organ tumor', 'neoplasm of Male reproductive system', 'male reproductive organ tumour', 'tumor of Male reproductive system', 'tumour of Male reproductive system', 'Male reproductive system tumor', 'neoplasm of male reproductive organ', 'tumour of the Male reproductive system', 'Male reproductive system neoplasm', 'Male reproductive system tumour']",,,,,,C3054,,,239.5,,,
mondo:0024607,congenital muscular dystrophy with cataracts and intellectual disability,"['muscular dystrophy, congenital, with cataracts and intellectual disability', 'MDCCAID']",0080197,617404,,C4479410,"['0.03108', '-0.4915', '0.2754', '0.743', '0.3213', '0.4766', '-0.4124', '0.809', '-0.1987', '-0.6665', '-0.0804', '-0.4207', '-0.2235', '1.009', '-0.2742', '0.2576', '0.4424', '0.422', '-0.4165', '-0.3247', '0.06946', '0.2822', '-0.0539', '-0.06946', '0.3638', '-0.2769', '-0.3215', '0.4014', '0.2163', '0.1205', '0.541', '-0.3533', '0.5464', '0.4604', '0.5425', '0.158', '0.1294', '-0.574', '0.303', '-1.25', '0.5396', '-0.4968', '-0.1757', '0.2015', '0.3533', '0.098', '0.582', '0.0334', '0.7905', '-0.623', '0.4028', '0.08765', '0.8784', '-0.5713', '0.4934', '-0.3386', '0.723', '0.556', '-0.6406', '-0.7456', '-0.1344', '-0.2725', '0.6396', '-0.4463', '-0.109', '0.751', '1.007', '0.7163', '0.4634', '0.6235', '-0.0839', '0.708', '0.58', '-0.4934', '1.1875', '0.3665', '-0.11255', '0.4688', '-0.313', '0.8433', '-0.07745', '-0.0319', '-0.794', '0.1543', '-0.1892', '-0.01917', '0.691', '0.3064', '1.2295', '0.5435', '-0.1257', '0.04074', '-0.1525', '0.505', '-0.0868', '-0.5605', '-0.0673', '-0.314', '-0.0786', '-0.582']",,0009149,,,,,
mondo:0024608,dientamoebiasis,"['Dientamoebiases', 'intestinal trichomoniasis', 'Dientamoeba caused disease or disorder']",946,,,,,,,D004030,,,,
mondo:0024609,vulvar squamous cell carcinoma,"['vulva epidermoid cell carcinoma', 'epidermoid cell carcinoma of the vulva', 'squamous cell carcinoma of the vulva', 'epidermoid carcinoma of vulva', 'vulvar squamous cell cancer', 'vulva squamous cell carcinoma', 'mammalian vulva squamous cell carcinoma', 'vulva epidermoid carcinoma', 'epidermoid carcinoma of the vulva', 'epidermoid cell carcinoma of vulva', 'vulvar squamous cell carcinoma', 'vulvar epidermoid cell carcinoma', 'squamous cell carcinoma of vulva', 'vulvar epidermoid carcinoma']",2101,,494448,C0280856,,C4052,1000624,,,,,
mondo:0024610,parasitic skin disorder,"['diseases, parasitic skin', 'skin disease, parasitic', 'disease, parasitic skin', 'parasitic skin diseases', 'parasitic skin disease']",,,,C0037280,,,,D012876,,,,
mondo:0024611,orbit neoplasm,"['tumor of orbit', 'orbital tumour', 'tumour of orbit', 'orbit neoplasm', 'neoplasm of orbit of skull', 'orbital neoplasm', 'tumor of orbit of skull', 'tumour of the orbit', 'orbital neoplasms', 'orbit tumour', 'orbital tumor', 'orbit tumor', 'tumor of the orbit', 'orbit of skull tumour', 'tumour of orbit of skull', 'orbit of skull tumor', 'neoplasm of orbit', 'neoplasm of the orbit']",,,,,,C3290,,,,,,
mondo:0024612,manic bipolar affective disorder,['manic bipolar affective disorder'],,,,,,C34805,,,,,,
mondo:0024613,bipolar depression,['bipolar depression'],,,,,,C34424,,,,,,
mondo:0024614,neurotic depression,['neurotic depression'],,,,,,C35369,,,,,,
mondo:0024615,T-cell and NK-cell neoplasm,"['T-cell and NK-cell neoplasm', 'T-cell neoplasm']",,,,C1336554,,C27908,,,,,,
mondo:0024616,tympanitis,['tympanic membrane inflammation'],,,,C0027134,,,,,,,,
mondo:0024617,xanthogranuloma,['xanthogranuloma'],,,,,,C27302,,,,,,
mondo:0024618,poliovirus infection,['Enterovirus C caused disease or disorder'],,,,C4303135,,,,,,,,
mondo:0024619,central nervous system infectious disorder,"['central nervous system infectious disorder', 'central nervous system infectious disease', 'infectious disease of central nervous system', 'central nervous system infection', 'infections, central nervous system']",,,,C0007684,,C27582,1001456,D002494,349.89,,,
mondo:0024620,meningitis caused by poliovirus,,,,,C4303134,,,,,,,,
mondo:0024621,serous cystadenocarcinoma,"['serous cystadenocarcinoma', 'serous adenocarcinoma']",,,,,,C3778,,,,,,
mondo:0024622,thyroid gland adenocarcinoma,"['thyroid gland adenocarcinoma', 'thyroid adenocarcinoma']",0080524,,,,,C27380,,,,,,
mondo:0024623,otorhinolaryngologic disease,"['ENT disease', 'diseases, otorhinolaryngological', 'otolaryngological disease', 'disease, otorhinolaryngological', 'otorhinolaryngologic disease', 'otolaryngologic disease', 'diseases, ENT', 'diseases, otolaryngological', 'ENT diseases', 'disease, otolaryngological', 'otolaryngologic diseases', 'disease, otorhinolaryngologic', 'otolaryngological diseases', 'diseases, otolaryngologic', 'disease, ENT', 'ear/nose/throat disease', 'otorhinolaryngological diseases', 'disease, otolaryngologic', 'otolaryngologic disorder', 'diseases, otorhinolaryngologic', 'otorhinolaryngological disease']",,,,C0395797,,C118420,,D010038,478.19,,,
mondo:0024625,disorder of lacrimal gland,"['disorder of lacrimal gland', 'lacrimal gland disease', 'disease of lacrimal gland', 'lacrimal gland disease or disorder']",,,,C0235228,,,,,,,,
mondo:0024626,defective phagocytic cell engulfment,,,,,C0398742,,,,,,,,
mondo:0024627,phagocytic cell dysfunction,,,,,C0398732,,,,,,,,
mondo:0024630,defective phagocytic cell chemotaxis,,,,,C0398735,,,,,279.8,,,
mondo:0024632,defective phagocytic cell opsonization,,,,,C0398733,,,,,,,,
mondo:0024633,hypertensive nephropathy,"['hypertensive nephropathy', 'HNP1']",,608026,,C0848548,,C4757,,C563161,403.90,,,
mondo:0024634,large intestine disorder,"['disorder of large intestine', 'disease of large intestine', 'large intestine disease or disorder']",,,,C0341321,,,,,,,,
mondo:0024635,small intestine disorder,"['disorder of small intestine', 'small intestine disease or disorder', 'disease of small intestine']",,,,C0341268,,,,,,,,
mondo:0024636,inflammation of heart layer,['heart layer inflammation'],,,,,,,,,429.89,,,
mondo:0024637,malignant soft tissue neoplasm,"['malignant soft tissue neoplasm', 'malignant neoplasm of soft tissue', 'malignant soft tissue tumor', 'malignant tumour of soft tissue', 'malignant soft tissue tumour', 'malignant tumor of the soft tissue', 'malignant tumour of the soft tissue', 'malignant tumor of soft tissue', 'malignant neoplasm of the soft tissue']",,,,,,C4867,,,,,,
mondo:0024638,pancreatic gastrinoma,['pancreatic gastrinoma'],,,,,,C95596,,,,,,
mondo:0024639,gastric enterochromaffin cell serotonin-producing neuroendocrine tumor,"['gastric enterochromaffin cell serotonin-producing neuroendocrine tumor', 'gastric EC-cell serotonin-producing neuroendocrine tumor', 'gastric EC-cell serotonin-producing neuroendocrine tumour', 'gastric EC cell serotonin-producing NET']",,,,C3274137,,C27443,,,,,,
mondo:0024642,gastric neuroendocrine tumor G2,"['gastric NET G2', 'gastric neuroendocrine tumor G2']",,,,C3272407,,C95880,,,,,,
mondo:0024643,myocardial disorder,"['myocardial disorder', 'myocardium disease or disorder', 'disease of myocardium', 'disorder of myocardium', 'myocardium disease']",,,,,,C35544,,,,,,
mondo:0024644,myocardial ischemia,"['heart disease, ischaemic', 'disease, ischemic heart', 'ischemic disease of myocardium', 'myocardium ischemic disease', 'heart disease, ischemic', 'IHD', 'ischaemic disease of myocardium', 'diseases, ischemic heart', 'heart diseases, ischaemic', 'heart diseases, ischemic', 'ischemic heart disease', 'disease, ischaemic heart', 'ischemia, myocardial', 'myocardial Ischemias', 'ischemic heart diseases', 'ischaemic heart disease', 'diseases, ischaemic heart', 'ischaemic heart diseases', 'ischemias, myocardial', 'myocardium ischaemic disease']",,,,C0151744,,C50625,1001375,D017202,,I20-I25,,
mondo:0024645,retroperitoneal neoplasm,"['tumor of retroperitoneal space', 'neoplasm of retroperitoneal space', 'retroperitoneal space tumor', 'retroperitoneal neoplasm', 'tumour of retroperitoneal space', 'retroperitoneal space tumour']",,,,,,C3357,,,,,,
mondo:0024647,urolithiasis,['urinary stones'],0080653,,,C0451641,,C114688,,D052878,,N21,,
mondo:0024648,optic tract meningioma,"['meningioma of the optic tract', 'meningioma of visual pathway', 'meningioma of the visual pathway', 'visual pathway meningioma', 'optic tract meningioma', 'meningioma of optic tract', 'optic tract meningioma (disease)']",,,,C1336972,,C5587,,,,,,
mondo:0024649,optic tract astrocytoma,"['optic tract astrocytoma (excluding glioblastoma)', 'visual pathway astrocytoma', 'astrocytoma (excluding glioblastoma) of optic tract', 'optic tract astrocytoma']",,,,C1336971,,C7533,,,,,,
mondo:0024650,drug-induced osteoporosis,,,,,,,,,,733.09,,,
mondo:0024651,corticosteroid-induced osteoporosis,,,,,C1272167,,,,,733.09,,,
mondo:0024652,embryonic cyst of fallopian tube,,,,,,,,,,,Q50.4,,
mondo:0024653,skull neoplasm,"['tumour of skull', 'neoplasm of skull', 'skull neoplasm', 'tumor of skull', 'neoplasm of the skull', 'tumour of the skull', 'skull tumour', 'skull tumor', 'tumor of the skull']",,,,C0037305,,C3375,,D012888,239.2,,,
mondo:0024654,skull disorder,"['disease of skull', 'disorder of skull', 'skull disorder', 'skull disease', 'skull disease or disorder']",,,,C1290854,,C27655,,,,,,
mondo:0024655,rheumatic pericarditis,,,,,C0264747,,,,,,,,
mondo:0024656,colorectal lymphoma,"['large intestine lymphoma', 'colorectal lymphoma', 'large intestinal lymphoma', 'lymphoma of large intestine', 'primary colorectal lymphoma']",,,,C3272822,,C96498,,,,,,
mondo:0024658,extrahepatic bile duct sarcoma,"['extrahepatic bile duct sarcoma', 'sarcoma of the extrahepatic bile duct', 'sarcoma of extrahepatic bile duct']",,,,C2205442,,C5029,,,,,,
mondo:0024659,colorectal Kaposi sarcoma,"['large intestinal Kaposi sarcoma', 'large intestine Kaposi^s sarcoma (disease)', 'colorectal Kaposi sarcoma']",,,,C3272833,,C96510,,,,,,
mondo:0024660,tubular adenoma,"['tubular adenoma', 'adenoma, tubular cell, benign']",,,,C0334292,,C4133,,,,,,
mondo:0024661,tubulovillous adenoma,['tubulovillous adenoma'],,,,C0334307,,C4143,,,,,,
mondo:0024662,colorectal tubulovillous adenoma,"['tubulovillous adenoma of large bowel', 'large bowel tubulovillous adenoma', 'tubulovillous adenoma of the large bowel', 'colorectal tubulovillous adenoma']",,,,C1333118,,C5675,,,,,,
mondo:0024663,primary skin meningioma,"['primary meningioma of skin', 'primary meningioma of the skin', 'primary cutaneous meningioma', 'primary skin meningioma']",,,,,,C5277,,,,,,
mondo:0024664,"hypertension, pregnancy-induced","['gestational hypertension', 'induced hypertension, pregnancy', 'pregnancy induced hypertension', 'induced Hypertensions, pregnancy', 'pregnancy transient hypertension', 'transient hypertension, pregnancy', 'hypertensions, pregnancy induced', 'hypertension-associated pregnancy disorder', 'hypertension, pregnancy induced', 'pregnancy-induced hypertension', 'hypertension, gestational', 'hypertension, pregnancy transient', 'hypertension associated disorders of pregnancy']",,,,,,C9243,,D046110,,,,
mondo:0024665,indeterminate sex and/or pseudohermaphroditism,,,,,,,,,,752.7,Q56,,
mondo:0024666,benign epithelial skin neoplasm,"['benign epithelial skin neoplasm', 'benign epithelial skin tumor', 'benign epithelial skin tumour', 'benign skin epithelium neoplasm', 'benign skin epithelium tumor', 'epithelial skin neoplasm, benign', 'benign skin epithelium tumour']",,,,C0345981,,C7341,,,,,,
mondo:0024673,skin lymphangioma,"['cutaneous lymphangioma', 'skin lymphangioma']",,,,C1333176,,C27509,,,,,,
mondo:0024674,Pancoast syndrome,"['Pancoast syndrome', 'tumor, Pancoast', 'Pancoast tumour', 'syndrome, Pancoast^s', 'Pancoasts syndrome', 'Pancoast tumor', 'syndrome, Pancoast']",,,,C0030271,,C55815,,D010178,,,,
mondo:0024675,adult kidney Wilms tumor,"['kidney Wilms tumour of adults', 'adult renal Wilms^ tumor', 'adult kidney adenosarcoma', 'adenosarcoma of the adult kidney', 'adult kidney Wilms tumor', 'adult renal Wilms tumor', 'adenosarcoma of adult kidney', 'adult renal Wilms tumour', 'adult nephroblastoma', 'kidney Wilms tumor of adults', 'adult renal Wilms^ tumour', 'adult renal adenosarcoma']",,,,C1332219,,C6180,,,,,,
mondo:0024676,childhood kidney Wilms tumor,"['childhood kidney Wilms tumor', 'Wilms tumour', 'childhood Wilms tumor', 'kidney Wilms tumor', 'childhood renal Wilms tumor', 'Wilms tumor', 'childhood renal Wilms^ tumor', 'childhood renal Wilms tumour', 'childhood Wilms tumour', 'kidney Wilms tumour', 'childhood renal Wilms^ tumour']",,,,C1333015,,C27730,,,,,,
mondo:0024677,pancreatic insulinoma,"['beta-cell tumors', 'insulin-producing tumour of islet cells', 'adenoma, beta cell', 'Insulomas', 'adenomas, beta-cell', 'adenoma, beta-cell', 'beta cell tumor', 'beta-cell adenoma', 'insuloma', 'islet cell adenoma', 'insulinoma', 'beta-cell adenomas', 'Insulinomas', 'beta cell tumour', 'beta-cell tumour', 'insulinoma tumour suppressor GENE locus', 'insulinoma tumor suppressor GENE locus', 'tumor, beta-cell', 'beta-cell tumor', 'tumors, beta-cell', 'beta-cell tumours', 'pancreatic insulinoma']",3892,,,,,C95598,0000549,D007340,,,10022498,0012197
mondo:0024685,Philadelphia-positive myelogenous leukemia,"['Ph1-positive myeloid leukaemia', 'Ph1-positive myelocytic leukaemia', 'Ph1-positive myelogenous leukemia', 'Philadelphia-positive myelocytic leukaemia', 'Philadelphia-positive myelocytic leukemia', 'Philadelphia-positive myelogenous leukemia', 'Philadelphia-positive myeloid leukaemia', 'Ph1-positive myeloid leukemia', 'Philadelphia-positive granulocytic leukaemia', 'Ph1-positive myelogenous leukaemia', 'Philadelphia-positive myeloid leukemia', 'Ph1-positive myelocytic leukemia', 'Ph1-positive granulocytic leukemia', 'Ph1-positive granulocytic leukaemia', 'Philadelphia-positive granulocytic leukemia']",,,,C0023476,,C3177,,,,,,
mondo:0024686,"tenosynovial giant cell tumor, diffuse type","['diffuse giant cell tumour of Tenosynovium', 'diffuse giant cell neoplasm of the Tenosynovium', 'diffuse giant cell neoplasm of Tenosynovium', 'diffuse pigmented villonodular synovitis', 'localized pigmented villonodular synovitis', 'diffuse giant cell tumour of tendon sheath', 'TSGCT', 'diffuse tenosynovial giant cell tumour', 'diffuse giant cell tumor of Tenosynovium', 'tenosynovial giant cell tumors', 'localised pigmented villonodular synovitis', 'tenosynovial giant cell tumour', 'tenosynovial giant cell tumor, diffuse type', 'diffuse tenosynovial giant cell neoplasm', 'tenosynovial giant cell tumour diffuse type', 'diffuse-type giant cell tumor', 'diffuse giant cell tumour of the Tenosynovium', 'pigmented villonodular synovitis', 'diffuse giant cell neoplasm of tendon sheath', 'TGCT', 'tenosynovial giant cell tumor diffuse type', 'tenosynovial giant cell tumor', 'diffuse-type giant cell tumour', 'villous tenosynovitis', 'villonodular synovitis', 'diffuse giant cell tumor of the Tenosynovium', 'diffuse giant cell tumor of tendon sheath', 'diffuse tenosynovial giant cell tumor', 'tenosynovial giant cell tumours', 'diffuse-type GCT']",9898,,66627,C0039106,,C3401,1001106,D013586,719.28,M12.2,,
mondo:0024711,malignant mixed epithelial stromal tumor of the kidney,"['malignant mixed epithelial stromal tumor of the kidney', 'mixed epithelial stromal tumour of the kidney, malignant', 'malignant MEST', 'mixed epithelial stromal tumor of the kidney, malignant']",,,,C1334602,,C37265,,,,,,
mondo:0024715,benign synovial neoplasm,"['benign tumour of the synovium', 'benign neoplasm of the synovium', 'benign neoplasm of synovium', 'benign synovial tumour', 'benign synovioma', 'benign synovial tumor', 'benign tumour of synovium', 'synovium neoplasm, benign', 'synovioma, benign', 'benign tumor of the synovium', 'benign synovial neoplasm', 'benign tumor of synovium']",,,,C0221289,,C3829,,,,,,
mondo:0024744,childhood choroid plexus neoplasm,"['pediatric choroid plexus neoplasm', 'choroid plexus neoplasm', 'childhood choroid plexus neoplasm', 'choroid plexus neoplasm of childhood', 'paediatric choroid plexus neoplasm']",,,,,,C42080,,,,,,
mondo:0024746,immature teratoma,"['embryonal teratoma', 'hrade 2 Teratoma', 'immature teratoma']",,,,,,C4286,,,,,,
mondo:0024757,cardiovascular neoplasm,"['tumour of cardiovascular system', 'cardiovascular system tumor', 'cardiovascular system tumour', 'cardiovascular neoplasm', 'tumor of cardiovascular system', 'cardiovascular tumor', 'cardiovascular tumour', 'neoplasm of cardiovascular system']",,,,,,C4784,,,,,,
mondo:0024770,"autoinflammatory syndrome, familial, X-linked, Behcet-like 2","['AIFBL2', 'autoinflammatory syndrome, familial, X-linked, Behcet-like 2', 'deficiency 1n ELF4, X-linked']",,301074,,,,,,,,,,
mondo:0024771,"myopathy, distal, 7, adult-onset, X-linked","['myopathy, distal, 7, adult-onset, X-linked', 'MPD7']",,301075,,,,,,,,,,
mondo:0024772,"intellectual developmental disorder, X-linked, syndromic, Pilorge type","['intellectual developmental disorder, X-linked, syndromic, Pilorge type', 'MRXSP']",0070422,301076,,,,,,,,,,
mondo:0024773,"spermatogenic failure, X-linked, 4","['spermatogenic failure, X-linked, 4', 'SPGFX4']",,301077,,,,,,,,,,
mondo:0024777,"immunodeficiency 98 with autoinflammation, X-linked","['IMD98', 'immunodeficiency 98 with autoinflammation, X-linked', 'inflammation, neutropenia, bone marrow failure, and lymphoproliferation caused by TLR8', 'X-linked immunodeficiency with autoinflammation']",,301078,,,,,,,,,,
mondo:0024781,immunodeficiency 102,"['IMD102', 'immunodeficiency 102', 'SASH3 deficiency']",,301082,,,,,,,,,,
mondo:0024797,adult brain stem neoplasm,"['neoplasm of adult brainstem', 'neoplasm of the adult brainstem', 'tumour of the adult brainstem', 'adult brain stem tumour', 'brainstem neoplasm of adults', 'tumor of the adult brainstem', 'neoplasm of adult brain stem', 'adult brainstem neoplasm', 'tumor of the adult brain stem', 'tumour of the adult brain stem', 'adult brain stem tumor', 'tumor of adult brainstem', 'adult brainstem tumour', 'adult brain stem neoplasm', 'neoplasm of the adult brain stem', 'tumour of adult brainstem', 'tumor of adult brain stem', 'tumour of adult brain stem', 'adult brainstem tumor']",,,,C1332192,,C5967,,,,,,
mondo:0024813,pulmonary sulcus neoplasm,"['pulmonary sulcus tumor', 'pulmonary sulcus tumour', 'pulmonary sulcus neoplasm']",,,,,,C27710,,,,,,
mondo:0024857,immature extragonadal teratoma,"['malignant extragonadal teratoma', 'immature extragonadal teratoma', 'primary malignant extragonadal teratoma', 'extragonadal primary malignant teratoma']",,,,C0855163,,C8884,,,,,,
mondo:0024861,mixed teratoma and seminoma,['mixed teratoma and seminoma'],,,,,,C9010,,,,,,
mondo:0024863,small size posterior uveal melanoma,['small size posterior uveal melanoma'],,,,C0278867,,C9089,,,,,,
mondo:0024864,medium/large size posterior uveal melanoma,['medium/large size posterior uveal melanoma'],,,,C0278868,,C9090,,,,,,
mondo:0024868,metastatic carcinoma in the adrenal medulla,"['metastatic carcinoma to the adrenal medulla', 'metastatic carcinoma in the adrenal medulla']",,,,C1334717,,C9276,,,,,,
mondo:0024873,clitoral carcinoma,"['carcinoma of clitoris', 'clitoral carcinoma', 'carcinoma of the clitoris', 'clitoral cancer', 'clitoris carcinoma']",,,,C1333070,,C9362,,,,,,
mondo:0024876,tendon sheath disorder,"['disorder of tendon sheath', 'tendon sheath disease or disorder', 'disease of tendon sheath']",,,,C0729734,,,,,727.9,,,
mondo:0024877,clitoris neoplasm,"['tumor of clitoris', 'tumour of clitoris', 'clitoris tumor', 'clitoris tumour', 'neoplasm of clitoris']",,,,C1263793,,,,,239.5,,,
mondo:0024878,secondary carcinoma,['secondary carcinoma'],,,,C0085668,,C36310,,,,,,
mondo:0024879,metastatic carcinoma,['metastatic carcinoma'],,,,C1384494,,C3482,,,,,,
mondo:0024880,metastatic malignant neoplasm,"['metastatic neoplasm, malignant', 'metastatic malignant neoplasm', 'metastatic cancer']",,,,,,C36263,,,,,,
mondo:0024881,secondary malignant neoplasm,"['secondary cancer', 'secondary malignant neoplasm', 'secondary malignancy']",,,,,,C4968,,,199.1,,,
mondo:0024882,secondary neoplasm,"['secondary tumour', 'secondary neoplasm', 'secondary tumor']",,,,,,C36255,,,,,,
mondo:0024883,metastatic neoplasm,"['metastatic disease', 'metastatic tumour', 'metastatic neoplasm', 'metastatic tumor']",,,,,,C3261,,,,,,
mondo:0024884,metastatic carcinoma in the bone,"['metastatic carcinoma in the bone', 'metastatic carcinoma to the bone']",,,,C0700110,,C36082,,,,,,
mondo:0024885,malignant ovarian serous tumor,"['malignant ovarian serous tumor', 'ovarian serous tumor, malignant']",,,,,,C40025,,,,,,
mondo:0024886,serous adenofibroma,['serous adenofibroma'],,,,C0334498,,C67090,,,,,,
mondo:0024888,mesonephric neoplasm,"['tumour of mesonephric duct', 'mesonephric tumour', 'Wolffian duct neoplasm', 'mesonephric duct tumor', 'tumor of mesonephric duct', 'Wolffian duct tumor', 'mesonephroma', 'neoplasm of mesonephric duct', 'mesonephric duct tumour', 'mesonephric neoplasm', 'mesonephric tumor', 'Wolffian duct tumour']",,,,,,C4295,,,,,,
mondo:0024889,benign mesonephroma,"['Wolffian duct adenoma', 'mesonephric neoplasm, benign', 'benign Mesonephroma', 'Mesonephroma, benign', 'Mesonephroma, benign (morphologic abnormality)', 'mesonephric duct adenoma', 'mesonephric adenoma']",2616,,,C0334530,,C4294,,,,,,
mondo:0024890,pineal parenchymal cell neoplasm,"['neoplasm of pineal gland', 'neoplasm of the pineal gland', 'pineal parenchymal cell tumour', 'pineal parenchymal neoplasm', 'pineal parenchymal cell tumor', 'tumor of pineal gland', 'pineocytic tumour', 'tumour of pineal gland', 'pineal parenchymal tumor', 'pineal gland tumour', 'pineocytic neoplasm', 'pineal parenchymal tumour', 'pineocytic tumor', 'pineal gland neoplasm', 'tumor of the pineal gland', 'pineal gland tumor', 'pineal parenchymal cell neoplasm', 'tumour of the pineal gland']",,,,C0031941,,C6965,,,,,,
mondo:0024891,non-infectious meningitis,,,,,C0393442,,,,,,,,
mondo:0024892,soft tissue amyloid neoplasm,"['amyloid tumour (morphologic abnormality)', 'soft tissue amyloid tumour', 'amyloid tumor', 'soft tissue amyloid tumor', 'soft tissue amyloid neoplasm', 'amyloid tumour', 'amyloid tumor (morphologic abnormality)', 'amyloid neoplasm']",6755,,,C1706802,,C8323,,,714.32,,,
mondo:0024893,toxocara canis infection (canine roundworms),"['Toxocara catis infection (feline roundworms)', 'Human infection with the larvae of canine or feline roundworms']",,,,C2930846,,,,C531834,,,,
mondo:0024905,bird disease,"['bird disease', 'Avian diseases', 'Avian disease', 'diseases, Avian', 'disease, Avian', 'diseases, Bird', 'disease, Bird']",,,,C0005591,,,,D001715,,,,
mondo:0024912,cat disease,"['diseases, Cat', 'Feline diseases', 'disease, Cat', 'Feline disease', 'disease, Feline', 'cat disease', 'diseases, Feline']",,,,C0007350,,,,D002371,,,,
mondo:0024913,cattle disease,"['diseases, cattle', 'bovine diseases', 'disease, cattle', 'disease, bovine', 'cattle disease', 'diseases, bovine', 'bovine disease']",,,,C0007453,,,,D002418,,,,
mondo:0024919,dog disease,"['canine disease', 'disease, canine', 'disease, Dog', 'diseases, Dog', 'diseases, canine', 'dog disease', 'canine diseases']",,,,C0012979,,,,D004283,,,,
mondo:0024934,fish disease,"['fish disease', 'diseases, fish', 'disease, fish']",,,,C0016154,,,,D005393,,,,
mondo:0024935,foot rot,"['rot, foot', 'foot Rots', 'Rots, foot']",,,,C0016513,,,,D005535,,,,
mondo:0024945,"hepatitis, non-human animal","['Hepatitides, animal', 'animal Hepatitides', 'animal Hepatitis']",,,,,,,,D006520,,,,
mondo:0024950,horse disease,"['disease, horse', 'equine disease', 'equine diseases', 'diseases, equine', 'horse disease', 'disease, equine', 'diseases, horse']",,,,C0019940,,,,D006734,,,,
mondo:0024953,"lameness, non-human animal","['animal Lamenesses', 'disorder, animal Gait', 'animal lameness', 'Lamenesses, animal', 'animal Gait disorder', 'Gait disorder, animal', 'Gait disorders, animal', 'disorders, animal Gait', 'animal Gait disorders']",,,,,,,,D007794,,,,
mondo:0024954,"larva migrans, visceral","['larva Migran, visceral', 'Migran, visceral larva', 'visceral larva Migran', 'visceral larva migrans', 'migrans, visceral larva', 'visceral larva migrans syndrome']",,,,,,,,D007816,,,,
mondo:0024965,"muscular dystrophy, non-human animal","['dystrophies, animal muscular', 'animal muscular dystrophies', 'animal muscular dystrophy', 'dystrophy, animal muscular', 'muscular dystrophies, animal']",,,,C0026851,,,,D009137,,,,
mondo:0024969,"parasitic disease, non-human animal","['diseases, animal parasitic', 'disease, animal parasitic', 'animal parasitic diseases', 'parasitic disease, animal', 'animal parasitic disease', 'parasitic infectious disease, non-human animal']",,,,C0030500,,,,D010273,,,,
mondo:0024971,parturient paresis,"['parturient Pareses', 'milk fever, animal', 'paresis, parturient', 'milk fever', 'fever, animal milk', 'animal milk fever', 'Pareses, parturient']",,,,C0030612,,,,D010319,,,,
mondo:0024973,"pneumonia, atypical interstitial, of cattle","['adenomatosis, pulmonary, bovine', 'pulmonary Adenomatoses, bovine', 'atypical interstitial pneumonia of cattle', 'bovine pulmonary Adenomatoses', 'pulmonary adenomatosis, bovine', 'fever, Fog', 'emphysema, acute bovine pulmonary', 'Fog fever', 'adenomatosis, bovine pulmonary', 'bovine pulmonary adenomatosis', 'Adenomatoses, bovine pulmonary']",,,,,,,,D011016,,,,
mondo:0024981,rodent disease,"['diseases, Rodent', 'disease, Rodent', 'rodent disease']",,,,C0035801,,,,D012376,,,,
mondo:0024982,"salmonella infections, animal","['Salmonella infection, animal', 'infection, animal Salmonella', 'salmonellosis, non-human animal', 'infections, animal Salmonella', 'animal Salmonella infections', 'animal Salmonella infection']",,,,C0036118,,,,D012481,,,,
mondo:0024985,sheep disease,"['diseases, sheep', 'sheep disease', 'diseases, Ovine', 'disease, Ovine', 'Ovine diseases', 'Ovine disease', 'disease, sheep']",,,,C0036946,,,,D012757,,,,
mondo:0024988,sex cord-stromal benign neoplasm,,0080368,,,,,,,,,,,
mondo:0024990,swine disease,"['swine disease', 'disease, swine', 'diseases, swine']",,,,C0039006,,,,D013553,,,,
mondo:0025003,goat disease,"['disease, caprine', 'diseases, caprine', 'goat disease', 'disease, goat', 'diseases, goat', 'caprine disease', 'caprine diseases']",,,,C0018018,,,,D015511,,,,
mondo:0025013,non-human primate disease,"['Primate disease', 'disease, Primate', 'diseases, Primate']",,,,C0242634,,,,D018419,,,,
mondo:0025028,vesicular stomatitis,"['Stomatitides, vesicular', 'stomatitis, vesicular', 'vesicular Stomatitides']",,,,C0266999,,,,D054243,,,,
mondo:0025030,digital dermatitis in cattle,"['papillomatous digital dermatitis', 'foot Warts, bovine', 'bovine hairy footwarts', 'bovine digital Dermatitides', 'Papillomatoses, digital', 'Dermatitides, bovine digital', 'bovine hairy footwart', 'hairy footwarts, bovine', 'hairy footwart, bovine', 'digital Dermatitides, Ovine', 'bovine foot Warts', 'foot wart, bovine', 'digital Papillomatoses', 'digital dermatitis, papillomatous', 'Dermatitides, digital', 'Ovine digital Dermatitides', 'digital dermatitis, Ovine', 'bovine digital dermatitis', 'digital Dermatitides, bovine', 'footwarts, bovine hairy', 'digital papillomatosis', 'papillomatosis, digital', 'dermatitis, bovine digital', 'footwart, bovine hairy', 'dermatitis, digital', 'digital dermatitis, bovine', 'wart, bovine foot', 'papillomatous digital Dermatitides', 'Ovine digital dermatitis', 'digital Dermatitides, papillomatous', 'digital Dermatitides', 'Warts, bovine foot', 'bovine foot wart']",,,,,,,,D058066,,,,
mondo:0025061,edema disease of swine,"['swine edema diseases', 'swine oedema disease', 'swine edema disease', 'swine oedema diseases']",,,,C0013605,,,,D004488,,,,
mondo:0025062,"encephalomyelitis, enzootic porcine","['enzootic porcine encephalomyelitis', 'disease, Teschen', 'porcine poliomyelitis', 'disease, Talfan', 'porcine encephalomyelitis, enzootic', 'poliomyelitis, porcine', 'Teschen disease', 'Talfan disease']",,,,,,,,D004682,,,,
mondo:0025066,"epidermitis, exudative, of swine","['swine exudative dermatitis', 'exudative dermatitis of swine', 'disease, greasy pig', 'swine exudative Dermatitides', 'Epidermitis, exudative of swine', 'greasy pig disease']",,,,C0014521,,,,D004818,,,,
mondo:0025082,"helminthiasis, animal","['Helminthiases, animal', 'animal Helminthiases', 'animal helminthiasis']",,,,C0018891,,,,D006374,,,,
mondo:0025085,"hepatitis, viral, animal",,,,,,,,,D006524,,,,
mondo:0025086,"hip dysplasia, canine","['canine hip dysplasia', 'dysplasia, canine hip']",,,,C0019556,,,,D006619,,,,
mondo:0025087,classical swine fever,"['swine fever', 'cholera, Hog', 'Hog cholera', 'swine fever, classical']",,,,C0019841,,,,D006691,,,,
mondo:0025089,infectious bovine rhinotracheitis,"['Rhinotracheitis, infectious bovine', 'infectious bovine Rhinotracheitides', 'Rhinotracheitides, infectious bovine', 'bovine Rhinotracheitis, infectious', 'bovine Rhinotracheitides, infectious']",,,,C0021334,,,,D007241,,,,
mondo:0025095,"malaria, avian","['Avian malaria', 'Avian Malarias', 'Malarias, Avian']",,,,C0024533,,,,D008289,,,,
mondo:0025096,malignant catarrh,"['malignant Catarrhs', 'malignant catarrhal fevers', 'catarrhal fevers, malignant', 'catarrh, malignant', 'catarrhal fever, malignant', 'Catarrhs, malignant', 'fever, malignant catarrhal', 'malignant catarrhal fever', 'fevers, malignant catarrhal']",,,,C0276241,,,,D008304,,,,
mondo:0025100,"mastitis, bovine","['bovine Mastitides', 'Mastitides, bovine', 'bovine mastitis']",,,,C0024895,,,1001765,D008414,,,,
mondo:0025102,monkey disease,"['monkey disease', 'disease, monkey', 'diseases, monkey']",,,,,,,,D008992,,,,
mondo:0025113,poultry disease,"['poultry disease', 'disease, poultry', 'diseases, poultry']",,,,C0032851,,,,D011201,,,,
mondo:0025114,"protozoan infections, animal","['infection, animal protozoan', 'animal protozoan infections', 'animal protozoan infection', 'protozoan infection, animal', 'infections, animal protozoan']",,,,C0033741,,,,D011529,,,,
mondo:0025129,swine erysipelas,"['erysipelas, swine']",,,,C0039007,,,,D013554,,,,
mondo:0025130,swine vesicular disease,"['vesicular disease, swine', 'vesicular diseases, swine', 'swine vesicular diseases']",,,,C0039010,,,,D013555,,,,
mondo:0025135,"tuberculosis, avian","['Avian Tuberculoses', 'Tuberculoses, Avian', 'Avian tuberculosis']",,,,C0041306,,,1001440,D014379,,,,
mondo:0025136,"tuberculosis, bovine","['bovine tuberculosis', 'bovine Tuberculoses', 'Tuberculoses, bovine']",,,,C0041307,,,1001441,D014380,,,,
mondo:0025138,vesicular exanthema of swine,"['swine vesicular exanthema', 'swine vesicular Exanthemas']",,,,C0042584,,,,D014720,,,,
mondo:0025139,white muscle disease,"['muscle disease, White', 'disease, White muscle', 'White muscle diseases', 'muscle diseases, White', 'diseases, White muscle']",,,,C0043153,,,,D014912,,,,
mondo:0025149,"encephalopathy, bovine spongiform","['BSE (bovine spongiform encephalopathy)', 'Mad cow diseases', 'bovine spongiform encephalopathy', 'bovine spongiform encephalitis', 'BSEs (bovine spongiform encephalopathy)', 'spongiform encephalopathy, bovine', 'Mad cow disease', 'encephalitis, bovine spongiform']",,,,,,,,D016643,,,,
mondo:0025152,non-human ape disease,"['Pongidae diseases', 'ape disease', 'Pongidae disease', 'diseases, ape', 'disease, ape', 'disease, Pongidae', 'diseases, Pongidae']",,,,C0242635,,,,D018420,,,,
mondo:0025159,"pneumonia of swine, mycoplasmal","['enzootic pneumonia of swine', 'swine enzootic pneumonia', 'Mycoplasmal pneumonia of swine', 'Mycoplasma pneumonia of pigs', 'enzootic pneumonia of pigs', 'pneumonia of swine, enzootic', 'swine Mycoplasma pneumonia', 'Mycoplasma pneumonia of swine', 'swine Mycoplasmal pneumonia']",,,,C1258090,,,,D045729,,,,
mondo:0025163,white heifer disease,"['disease, White heifer']",,,,C0043152,,,,D050072,,,,
mondo:0025167,"reticuloendotheliosis, avian","['Avian reticuloendotheliosis', 'Avian Reticuloendothelioses', 'Reticuloendothelioses, Avian']",,,,C0276487,,,,D055761,,,,
mondo:0025193,oculopharyngodistal myopathy,"['oculopharyngeal distal myopathy', 'OPDM', 'oculopharyngodistal myopathy', 'faciooculolaryngopharyngeal myopathy with distal and respiratory involvement']",0081296,,98897,C1834014,"['-0.08514', '0.04803', '0.02617', '-0.4001', '-0.3823', '-0.6714', '0.3228', '0.3425', '-0.944', '-0.4263', '0.0307', '0.1289', '-0.508', '0.607', '0.1674', '0.1359', '0.0003996', '-0.054', '-0.1355', '-0.5615', '0.1359', '-0.1947', '-0.09515', '0.674', '0.15', '-0.0807', '0.1573', '-0.337', '-0.008804', '0.1267', '0.3557', '0.3333', '0.2167', '-0.2644', '0.2345', '-0.1654', '-0.1051', '-0.0736', '0.2438', '-0.2147', '-0.1636', '-0.653', '-0.01729', '0.057', '0.007725', '-0.5425', '-0.2053', '0.3245', '0.11523', '0.1926', '-0.2369', '0.06635', '0.05435', '-0.753', '0.1059', '-0.7764', '0.07623', '0.185', '0.1451', '-0.4927', '0.05917', '0.1337', '-0.378', '-0.0433', '-0.583', '0.06726', '-0.07336', '0.6636', '-0.1587', '0.4402', '-0.1821', '-0.07263', '-0.05988', '0.2019', '0.4353', '0.1609', '0.2664', '0.148', '-0.08795', '-0.006523', '0.4058', '-0.02026', '0.855', '0.2451', '-0.11914', '0.1976', '-0.1968', '0.1498', '0.3394', '0.257', '0.3235', '0.07806', '0.2842', '0.5635', '0.9004', '0.2378', '0.2615', '0.1231', '-0.168', '0.0962']",,,C563508,,,,
mondo:0025263,"strongyle infections, equine","['equine strongyle infections', 'infections, equine strongyle', 'equine Strongyloses', 'Strongylosis, equine', 'infection, equine strongyle', 'Strongyloses, equine', 'strongyle infection, equine', 'equine strongyle infection', 'equine Strongylosis']",,,,C0038459,,,,D013319,,,,
mondo:0025270,"toxoplasmosis, non-human animal","['animal toxoplasmosis', 'Toxoplasmoses, animal', 'animal Toxoplasmoses']",,,,C0040559,,,,D014124,,,,
mondo:0025271,"trypanosomiasis, bovine","['Trypanosomiases, bovine', 'bovine trypanosomiasis', 'bovine Trypanosomiases']",,,,C0041230,,,,D014354,,,,
mondo:0025293,poult enteritis mortality syndrome,"['mortality syndrome, spiking', 'spiking mortality syndrome']",,,,C1135821,,,,D031261,,,,
mondo:0025294,tick-borne infectious disease,"['infections, Tick-borne', 'infections, Tick borne', 'Tick-borne infections', 'Tick borne infections', 'infection, Tick-borne', 'Tick borne diseases', 'disease, Tick-borne', 'Tick-borne disease', 'diseases, Tick-borne', 'Tick-borne infection']",,,,,,,,D017282,,,,
mondo:0025303,anaplasmosis,"['human anaplasmosis', 'anaplasma caused disease or disorder', 'anaplasmoses']",,,,,,C128425,,D000712,082.49,,,
mondo:0025351,"multiple congenital anomalies-neurodevelopmental syndrome, X-linked","['multiple congenital anomalies-neurodevelopmental syndrome, X-linked, X-linked recessive', 'MCAND', 'Linked syndrome']",,301056,,,,,,,,,,
mondo:0025353,"developmental and epileptic encephalopathy, 90","['developmental and epileptic encephalopathy 90', 'developmental and epileptic encephalopathy 90, X-linked recessive, X-linked dominant', 'DEE90']",0070381,301058,,,,,,,,,,
mondo:0025354,"spermatogenic failure, X-linked, 3","['spermatogenic failure, X-linked, 3', 'spermatogenic failure, X-linked, 3, X-linked recessive', 'SPGFX3']",0112274,301059,,,,,,,,,,
mondo:0025356,"azoospermia, obstructive, with nephrolithiasis","['OAZON', 'azoospermia, obstructive, with nephrolithiasis, X-linked recessive']",,301060,,,,,,,,,,
mondo:0025369,Nairobi sheep disease,"['sheep disease, Nairobi', 'disease, Nairobi sheep']",,,,C0027345,,,,D009265,,,,
mondo:0025371,Parvoviridae infectious disease,"['Parvovirus infections', 'infection, Parvovirus', 'Parvoviridae caused disease or disorder', 'Parvoviridae infection', 'infections, Parvoviridae', 'infections, Parvovirus', 'Parvovirus infection', 'infection, Parvoviridae']",,,,,,,,D010322,078.89,,,
mondo:0025376,African horse sickness,"['sickness, African horse', 'Horsesickness, African', 'Sicknesses, African horse', 'horse sickness, African', 'plague, equine', 'horse Sicknesses, African', 'African horse Sicknesses', 'African Horsesickness', 'equine Plagues', 'African Horsesicknesses', 'Plagues, equine', 'equine plague', 'Horsesicknesses, African']",,,,C0001748,,,,D000355,,,,
mondo:0025377,African swine fever,"['swine fever, African', 'wart-Hog disease', 'wart Hog disease', 'wart-Hog diseases']",,,,C0001752,,,,D000357,,,,
mondo:0025381,avian leukosis,"['lymphoid leukosis', 'leukosis, Avian', 'Avian Leukoses', 'leukoses, Avian']",,,,C0004421,,,,D001353,,,,
mondo:0025382,"sarcoma, avian","['sarcomas, Avian', 'sarcoma, Rous', 'Rous sarcoma', 'Avian sarcoma', 'Avian sarcomas']",,,,,,,,D001357,,,,
mondo:0025385,bluetongue,"['blue tongue', 'tongue, blue']",,,,C0005866,,,,D001819,,,,
mondo:0025389,"brucellosis, bovine","['bovine Brucelloses', 'bang^s disease', 'bovine brucellosis', 'disease, bang^s', 'bang disease', 'Bangs disease', 'Brucelloses, bovine', 'disease, bang']",,,,,,,,D002007,,,,
mondo:0025397,canine distemper,"['distemper, canine', 'canine distemper', 'Distempers, canine', 'canine Distempers', 'Distempers']",,,,,,,,D004216,,,,
mondo:0025404,coronaviral enteritis of turkeys,"['Bluecomb of turkeys', 'enteritis, transmissible, of turkeys', 'transmissible enteritis of turkeys', 'coronaviral enteritis of turkeys']",,,,C0014342,,,,D004753,,,,
mondo:0025412,feline panleukopenia,"['Feline distemper', 'plague, Cat', 'Feline Distempers', 'ataxia, Feline', 'infectious enteritis, Feline', 'show fevers', 'fever, show', 'Feline Ataxias', 'Feline infectious Enteritides', 'agranulocytosis, Feline', 'Feline Agranulocytoses', 'distempers, Feline', 'enteritis, Feline infectious', 'infectious Enteritides, Feline', 'Feline ataxia', 'enteritides, Feline infectious', 'Feline Panleukopenias', 'fevers, show', 'Panleukopenias, Feline', 'agranulocytoses, Feline', 'Feline agranulocytosis', 'Panleukopenia, Feline', 'Cat Plagues', 'Cat plague', 'plagues, Cat', 'show fever', 'Feline infectious enteritis', 'ataxias, Feline', 'distemper, Feline']",,,,C0015765,,,,D005254,,,,
mondo:0025417,fowlpox,"['Diphtherias, fowl', 'fowl diphtheria', 'Birdpox', 'pox, fowl', 'fowl Diphtherias', 'Bird pox', 'Variola avium', 'pox, Bird', 'fowl pox', 'diphtheria, fowl', 'epithelioma contagiosum']",,,,,,,,D005586,,,,
mondo:0025419,furunculosis,"['boils', 'Furuncles', 'Furunculoses', 'furuncle']",,,,,,C34629,,D005667,,,,
mondo:0025420,"gastroenteritis, transmissible, of swine","['transmissible Gastroenteritides, swine', 'gastroenteritis, transmissible porcine', 'porcine gastroenteritis, transmissible', 'porcine transmissible Gastroenteritides', 'transmissible gastroenteritis of swine', 'swine transmissible Gastroenteritides', 'transmissible porcine Gastroenteritides', 'Gastroenteritides, porcine transmissible', 'gastroenteritis, swine transmissible', 'Gastroenteritides, transmissible porcine', 'porcine Gastroenteritides, transmissible', 'porcine transmissible gastroenteritis', 'Gastroenteritides, swine transmissible', 'transmissible Gastroenteritides, porcine', 'gastroenteritis, transmissible, porcine', 'gastroenteritis, porcine transmissible', 'transmissible gastroenteritis, swine', 'swine transmissible gastroenteritis', 'transmissible gastroenteritis, porcine', 'transmissible porcine gastroenteritis']",,,,C0017162,,,,D005761,,,,
mondo:0025425,"hepatitis, infectious canine","['Hepatitides, canine infectious', 'canine Hepatitis, infectious', 'canine infectious Hepatitis', 'infectious canine Hepatitis', 'infectious Hepatitis, canine', 'canine infectious Hepatitides', 'infectious Hepatitides, canine', 'Hepatitides, infectious canine', 'canine Hepatitides, infectious', 'infectious canine Hepatitides', 'Hepatitis, canine infectious']",,,,,,,,D006522,,,,
mondo:0025431,"keratoconjunctivitis, infectious","['Keratoconjunctivitides, infectious', 'infectious keratoconjunctivitis', 'infectious Keratoconjunctivitides']",,,,C0022576,,,,D007639,,,,
mondo:0025445,Wieacker-Wolff syndrome (spectrum),,,,,,,,,,,,,
mondo:0025449,paratuberculosis,"['Johne disease', 'Johnes disease', 'disease, Johne', 'Paratuberculoses', 'Johne^s disease', 'disease, Johne^s']",,,,C0030524,,,,D010283,,,,
mondo:0025453,"pneumonia, progressive interstitial, of sheep","['progressive interstitial pneumonia of sheep', 'Maedi']",,,,C0032306,,,,D011021,,,,
mondo:0025457,"pulmonary adenomatosis, ovine","['Adenomatoses, Ovine pulmonary', 'pulmonary carcinomas, Ovine', 'Ovine pulmonary carcinoma', 'adenomatosis, pulmonary, Ovine', 'Ovine pulmonary carcinomas', 'adenomatosis, pulmonary Ovine', 'pulmonary carcinoma, Ovine', 'adenomatosis, Ovine pulmonary', 'pulmonary Adenomatoses, Ovine', 'Jaagsiekte', 'pulmonary Ovine adenomatosis', 'Adenomatoses, pulmonary Ovine', 'pulmonary Ovine Adenomatoses', 'Ovine Adenomatoses, pulmonary', 'carcinomas, Ovine pulmonary', 'Ovine pulmonary adenomatosis', 'carcinoma, Ovine pulmonary', 'Ovine adenomatosis, pulmonary', 'Ovine pulmonary Adenomatoses']",,,,C0034049,,,,D011648,,,,
mondo:0025459,rinderpest,"['plague, cattle', 'cattle plague']",,,,C0035637,,,,D012301,,,,
mondo:0025478,"venereal tumors, veterinary","['tumor, veterinary venereal', 'venereal tumor, transmissible', 'tumor, transmissible venereal', 'transmissible venereal tumour', 'transmissible venereal tumor', 'veterinary venereal tumor', 'veterinary venereal tumors', 'veterinary venereal tumours', 'transmissible venereal tumors', 'transmissible venereal tumours', 'tumors, transmissible venereal', 'tumors, veterinary venereal', 'venereal tumor, veterinary', 'veterinary venereal tumour', 'venereal tumors, transmissible']",,,,C0042465,,,,D014685,,,,
mondo:0025483,"mammary neoplasms, animal","['mammary neoplasm', 'carcinomas, animal mammary', 'animal mammary neoplasms', 'neoplasm, animal mammary', 'mammary carcinoma, animal', 'neoplasms, animal mammary', 'animal mammary neoplasm', 'mammary neoplasm, animal', 'mammary carcinomas, animal', 'neoplasm, mammary', 'mammary neoplasms', 'animal mammary carcinoma', 'animal mammary carcinomas', 'neoplasms, mammary', 'carcinoma, animal mammary']",,,,,,,,D015674,,,,
mondo:0025484,simian acquired immunodeficiency syndrome,"['Simian acquired immune deficiency syndrome', 'AIDSs, Simian', 'Simian AIDS', 'Simian AIDSs', 'SAIDS', 'AIDS, Simian', 'Simian immunodeficiency virus caused monkey disease', 'Simian acquired immuno-deficiency syndrome', 'Simian acquired immuno deficiency syndrome']",,,,C0080151,,,,D016097,,,,
mondo:0025485,feline acquired immunodeficiency syndrome,"['Feline acquired immune deficiency syndrome', 'FAIDS', 'AIDS, Feline', 'Feline acquired immuno deficiency syndrome', 'Feline AIDS', 'Feline immunodeficiency virus caused cat disease', 'Feline acquired immuno-deficiency syndrome']",,,,C0079335,,,,D016181,,,,
mondo:0025487,murine acquired immunodeficiency syndrome,"['AIDS, murine', 'murine acquired immune deficiency syndrome', 'murine acquired immuno-deficiency syndrome', 'murine AIDS', 'murine AIDSs', 'MAIDS', 'murine acquired immuno deficiency syndrome']",,,,,,,,D016183,,,,
mondo:0025488,"leukemia, feline","['Feline leukemias', 'Feline leukemia', 'leukemias, Feline', 'Feline leukaemia']",,,,C0085164,,,,D016582,,,,
mondo:0025489,enzootic bovine leukosis,"['bovine lymphosarcoma', 'leukemias, bovine', 'lymphosarcoma, bovine', 'leukosis, enzootic bovine', 'bovine leukemias', 'lymphoma, bovine', 'leukoses, enzootic bovine', 'leukemia, bovine', 'bovine leukaemia', 'bovine Leukoses, enzootic', 'leukoses, bovine', 'bovine Leukoses', 'lymphosarcomas, bovine', 'leukosis, bovine', 'bovine leukemia', 'bovine leukosis', 'enzootic bovine Leukoses', 'bovine Lymphosarcomas', 'lymphomas, bovine', 'bovine leukosis, enzootic', 'bovine lymphoma', 'bovine Lymphomas']",,,,,,,1001315,D016583,,,,
mondo:0025491,feline infectious peritonitis,"['feline infectious peritonitides', 'infectious peritonitides, feline', 'peritonitis, feline infectious', 'FIP', 'infectious peritonitis, feline', 'peritonitis, infectious, feline']",,,,C0085306,,,,D016766,,,,
mondo:0025494,porcine reproductive and respiratory syndrome,"['porcine epidemic abortion and respiratory syndrome', 'PRRS', 'pig disease, blue-eared', 'swine infertility and respiratory syndrome', 'blue eared pig disease', 'swine disease, mystery', 'mystery swine disease', 'blue-eared pig disease']",,,,C0376538,,,,D019318,,,,
mondo:0025505,mink viral enteritis,"['mink viral enteritides', 'viral enteritides, mink', 'enteritides, mink viral', 'enteritis, infectious, of mink', 'viral enteritis, mink', 'enteritis, mink viral']",,,,C1720999,,,,D053489,,,,
mondo:0025506,porcine postweaning multisystemic wasting syndrome,"['postweaning multisystemic wasting syndrome, porcine', 'postweaning multisystemic wasting syndrome']",,,,C1721016,,,1000048,D053570,,,,
mondo:0025510,"pythiosis, non-human animal",,,,,C0276912,,,,D058968,,,,
mondo:0025511,inherited neuroendocrine tumor,"['hereditary neuroendocrine neoplasm', 'genetic neuroendocrine tumour', 'genetic neuroendocrine tumor']",,,271847,CN202530,,,,,,,,
mondo:0025512,type II hypersensitivity reaction disease,"['disorder of type II hypersensitivity', 'type II hypersensitivity disease']",417,,,,"['-0.243', '0.0735', '0.03647', '0.06537', '0.1447', '-0.1707', '0.004536', '0.03568', '-0.2698', '-0.00535', '-0.1278', '0.00979', '0.1544', '0.00766', '-0.069', '-0.05624', '-0.04266', '-0.12225', '-0.01697', '-0.3152', '0.0124', '-0.1014', '0.1752', '-0.1278', '0.0554', '-0.04205', '-0.04837', '-0.04608', '-0.08905', '-0.00654', '0.2085', '0.1532', '0.2378', '0.12177', '0.0668', '-0.2294', '-0.0415', '-0.12305', '0.04175', '-0.2812', '0.0712', '-0.2087', '-0.01522', '0.06976', '-0.03091', '-0.1316', '0.03973', '0.0394', '0.0885', '0.03757', '-0.05536', '-0.1016', '-0.03473', '0.065', '-0.0881', '-0.01613', '0.136', '-0.05692', '-0.1886', '0.09937', '-0.04526', '0.02902', '0.0931', '0.087', '0.03754', '0.1796', '0.2494', '0.05536', '-0.1964', '0.2217', '-0.2202', '0.02748', '0.05234', '-0.2079', '0.1687', '0.1852', '-0.0807', '0.0603', '-0.011635', '-0.12177', '0.08777', '0.0486', '-0.1816', '0.0952', '-0.1515', '-0.04166', '0.1213', '0.2357', '0.3118', '0.04822', '0.0527', '0.09973', '0.007904', '0.01407', '0.3538', '0.2319', '0.0739', '-0.2607', '0.03036', '0.03732']",,0005809,,,,,
mondo:0025513,autoimmune urticaria,,,,,C1304191,,,,,708.8,,,
mondo:0025514,livedoid vasculopathy,"['livedoid vasculopathy', 'livedoid vasculitis', 'livedo reticularis with summer ulcerations', 'segmental hyalinizing vasculopathy', 'livedo reticularis with winter ulcerations', 'livedo vasculitis']",0040099,,542643,C0343081,,,,D000090122,709.1,L95.0,,
mondo:0025556,isocyanate induced asthma,['isocyanates allergic asthma'],0040041,,,C1321273,,,,,506.3,,,
mondo:0025598,pneumonia caused by chlamydia,['Chlamydia caused pneumonia'],0040083,,,C0339959,,,,D061387,483.1,,,
mondo:0025622,"Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1",['CMTMA1'],,500013,,,,,,,,,,
mondo:0025667,limbal stem cell deficiency,,,,171673,C1561989,,,,,,,,
mondo:0025690,"microcephaly, epilepsy, and diabetes syndrome 2",['MEDS2'],,619278,,,,,,,,,,
mondo:0025691,dystonia 30,['DYT30'],,619291,,,,,,,,,,
mondo:0025699,Coffin-Siris syndrome 12,['CSS12'],0112370,619325,,,,,,,,,,
mondo:0025701,"leukodystrophy, hypomyelinating, 22",['HLD22'],0070402,619328,,,,,,,,,,
mondo:0025708,megacystis-microcolon-intestinal hypoperistalsis syndrome 2,['MMIHS2'],,619351,,,,,,,,,,
mondo:0025712,"angioedema, hereditary, 4",['HAE4'],,619360,,,,,,,,,,
mondo:0025713,"angioedema, hereditary, 7",['HAE7'],,619366,,,,,,,,,,
mondo:0025956,ovarian remnant syndrome,,,,,,,,,,,,,
mondo:0025986,megacystis-microcolon-intestinal hypoperistalsis syndrome,,,,,,,,,,,,,
mondo:0026045,prurigo nodularis,,,,,,,,,,,,,
mondo:0026404,"X inactivation, familial skewed, 1","['SXI1', 'X-inactivation, familial skewed', 'X-inactivation, familial skewed, 1', 'X INACTIVATION, FAMILIAL SKEWED, 1']",,300087,,,,,,C564716,,,,
mondo:0026426,"X inactivation, familial skewed, 2","['X INACTIVATION, FAMILIAL SKEWED, 2', 'X-inactivation, familial skewed, 2', 'SXI2']",,300179,,,,,,C564572,,,,
mondo:0026720,"mitochondrial complex 1 deficiency, nuclear type 12","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 12', 'mitochondrial complex i deficiency, nuclear type 12, X-linked recessive', 'MC1DN12']",0112099,301020,,,,,,,,,,
mondo:0026721,"mitochondrial complex 1 deficiency, nuclear type 30","['MC1DN30', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 30']",0112098,301021,,,,,,,,,,
mondo:0026722,Mullegama-Klein-Martinez syndrome,"['MULLEGAMA-KLEIN-MARTINEZ SYNDROME', 'Neurodevelopmental Disorder, X-Linked, With Craniofacial Abnormalities', 'MKMS']",0111845,301022,,,,,,,,,,
mondo:0026723,"intellectual developmental disorder, X-linked 108","['intellectual developmental disorder, X-linked 108, X-linked recessive', 'MRX108', 'Mental Retardation, X-Linked 108', 'INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 108']",0111844,301024,,,,,,,,,,
mondo:0026724,Paganini-Miozzo syndrome,"['Paganini-Miozzo syndrome, X-linked recessive', 'mental retardation, X-Linked, syndromic, Paganini-Miozzo type', 'MRXSPM', 'PAGANINI-MIOZZO SYNDROME']",0111843,301025,,,,,,,,,,
mondo:0026726,"nephrotic syndrome, type 20","['NPHS20', 'NEPHROTIC SYNDROME, TYPE 20']",0070357,301028,,,,,,,,,,
mondo:0026727,Shukla-Vernon syndrome,"['Shukla-Vernon syndrome, X-linked recessive', 'SHUVER', 'SHUKLA-VERNON SYNDROME']",0111841,301029,,,,,,,,,,
mondo:0026729,"congenital disorder of glycosylation, type ICC","['congenital disorder of glycosylation, type Icc, X-linked recessive', 'CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Icc', 'CDG1CC']",0111839,301031,,,,,,,,,,
mondo:0026730,Basilicata-Akhtar syndrome,"['Mental Retardation, X-Linked, Syndromic 36', 'MRXSBA', 'Mental Retardation, X-Linked, Syndromic, Basilicata-Akhtar Type', 'Basilicata-Akhtar syndrome, X-linked dominant', 'Basilicata-Akhtar syndrome']",0111838,301032,,,,,,,,,,
mondo:0026731,"hypothyroidism, congenital, nongoitrous, 8","['HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 8', 'CHNG8']",0111837,301033,,,,,,,,,,
mondo:0026732,"hypothyroidism, congenital, nongoitrous, 9","['hypothyroidism, congenital, nongoitrous, 9, X-linked recessive', 'HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 9', 'CHNG9']",0111835,301035,,,,,,,,,,
mondo:0026733,"intellectual developmental disorder, X-linked, syndromic, Hackmann-Di Donato type","['MRXSHD', 'intellectual developmental disorder, X-linked, syndromic, Hackman-Di Donato type, X-linked recessive', 'INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, HACKMANN-DI DONATO TYPE', 'Mental Retardation, X-Linked, With Marfanoid Habitus, 2']",,301039,,,,,,,,,,
mondo:0026762,"Wieacker-Wolff syndrome, female-restricted","['Wieacker-Wolff syndrome, female-restricted, X-linked dominant', 'WRWFFR', 'WIEACKER-WOLFF SYNDROME, FEMALE-RESTRICTED']",,301041,,,,,,,,,,
mondo:0026763,"holoprosencephaly 13, X-linked","['HOLOPROSENCEPHALY 13, X-LINKED', 'HPE13', 'holoprosencephaly 13, X-linked, X-linked recessive, X-linked dominant']",,301043,,,,,,,,,,
mondo:0026765,"congenital disorder of glycosylation, type IIr","['CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIr', 'CDG2R', 'congenital disorder of glycosylation, type IIr, X-linked recessive', 'CDG IIr']",,301045,,,,,,,,,,
mondo:0026767,"immunodeficiency 74, COVID-19-related, X-linked","['IMD74', 'IMMUNODEFICIENCY 74, COVID19-RELATED, X-LINKED', 'TLR7 deficiency', 'respiratory insufficiency due to SARS-CoV-2 viral infection', 'immunodeficiency 74, COVID19-related, X-linked, X-linked recessive']",0112063,301051,,,,,,,,,,
mondo:0026771,"developmental and epileptic encephalopathy, 85, with or without midline brain defects","['DEE85, with or without midline brain defects', 'epileptic encephalopathy, early infantile, 85, with or without midline brain defects', 'EIEE85', 'developmental and epileptic encephalopathy 85, with or without midline brain defects, X-linked dominant']",0070380,301044,,,,,,,,,,
mondo:0026777,VEXAS syndrome,"['VEXAS syndrome, somatic', 'VEXAS', 'vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic syndrome']",0080828,301054,596753,,,C181924,,,,,,
mondo:0027026,Buschke Lowenstein tumor,"['condyloma Acuminatum, Giant', 'Giant condyloma Acuminatum', 'Buschke-Lowenstein tumor', 'Giant condyloma of Buschke and Lowenstein', 'Giant condyloma Acuminatums', 'giant condyloma of Buschke and Lowenstein', 'Lowenstein tumor, Buschke', 'condyloma Acuminatums, Giant', 'anogenital type verrucous carcinoma', 'Buschke Lowenstein tumor', 'giant condyloma acuminatum involving the prepuce and glans penis', 'tumor, Buschke-Lowenstein', 'tumor, Buschke Lowenstein', 'Buschke-Lowenstein tumour', 'GCBL']",,,,C0276264,,C6371,,D062688,,,,
mondo:0027029,HHV-6 encephalitis,"['Human Herpesvirus 6 encephalitis', 'Variant B or HHV-6B', 'Variant A or HHV-6A']",,,,,,,,,,,,
mondo:0027048,"deafness, Y-linked 2","['DFNY2', 'deafness, y-linked 2, y-linked']",0111758,400047,,,,,,,,,,
mondo:0027068,"mitochondrial complex 1 deficiency, mitochondrial type 1","['MC1DM1', 'mitochondrial complex I deficiency, mitochondrial type 1']",0112101,500014,,,,,,,,,,
mondo:0027069,"mitochondrial complex 5 (ATP synthase) deficiency, mitochondrial type 1","['mitochondrial complex V (ATP synthase) deficiency, mitochondrial type 1', 'MC5DM1']",0111748,500015,,,,,,,,,,
mondo:0027091,xanthogranulomatous sialadenitis,"['sialadenitis, xanthogranulomatous']",,,,,,,,C536763,,,,
mondo:0027353,autosomal recessive dyskeratosis congenita 4,"['dyskeratosis congenita, autosomal recessive 4', 'DKCB4']",0070021,,,,,,,,,,,
mondo:0027407,Kleefstra syndrome 1,"['Kleefstra syndrome', 'chromosome 9q34.3 deletion syndrome', 'KLEFS1', '9q-syndrome', 'Kleefstra syndrome 1']",0070075,610253,,C0795833,"['-0.002518', '0.01534', '0.006287', '-0.00731', '0.00834', '-0.0142', '0.001932', '0.01581', '-0.00941', '-0.009865', '-0.011696', '-0.0003543', '0.01431', '0.01012', '-0.01323', '-0.01732', '-0.00787', '0.000863', '-0.01297', '-0.02309', '0.00639', '-0.00748', '0.0165', '-0.007088', '-0.00116', '-0.003819', '0.00431', '-0.01591', '0.013855', '-0.01718', '0.0272', '-0.002657', '0.01765', '0.015305', '-0.0013485', '-0.01288', '0.002794', '-0.00926', '-0.00993', '-0.02554', '0.01952', '-0.01721', '0.001775', '-0.0119', '-0.0007215', '-0.02852', '-0.007435', '0.01023', '0.01225', '0.000718', '0.001026', '0.006298', '-0.00133', '-0.00785', '-0.01872', '-0.00857', '0.0236', '-0.01019', '-0.0249', '-0.00609', '0.0151', '0.015236', '-0.006325', '0.003452', '-0.000858', '0.011986', '0.010605', '0.0217', '-0.00962', '0.02788', '-0.00548', '-0.006332', '0.011284', '-0.01344', '0.012054', '0.006226', '0.00777', '-0.00988', '-0.01666', '-0.01427', '-0.00237', '-0.010185', '-0.00557', '0.01306', '-0.0001721', '-8.45e-05', '0.01529', '0.014046', '0.02406', '0.002401', '0.01019', '0.01947', '-0.007156', '-0.006363', '0.04352', '0.013725', '0.012115', '-0.02452', '0.0002135', '0.01668']",C129976,,C563043,,,,
mondo:0027451,autosomal recessive cutis laxa type 2D,"['ARCL2D', 'autosomal recessive cutis laxa type IID', 'cutis laxa, autosomal recessive, type IID', 'cutis laxa, autosomal recessive, type 2D']",0070129,617403,,,,,,,,,,
mondo:0027462,autosomal recessive cutis laxa type 2C,"['autosomal recessive cutis laxa type IIC', 'cutis laxa, autosomal recessive, type 2C', 'cutis laxa, autosomal recessive, type IIC', 'ARCL2C']",0070140,617402,,,,,,,,,,
mondo:0027652,5-fluorouracil toxicity,,,,240839,,,,,,,,,
mondo:0027653,abacavir toxicity,,,,240841,,,,,,,,,
mondo:0027655,allopurinol toxicity,,,,240845,,,,,,,,,
mondo:0027664,cisplatin toxicity,,,,240863,,,,,,,,,
mondo:0027666,codeine toxicity,,,,240867,,,,,,,,,
mondo:0027667,efavirenz toxicity,,,,240869,,,,,,,,,
mondo:0027668,flucloxacilline toxicity,,,,240871,,,,,,,,,
mondo:0027675,irinotecan toxicity,,,,240885,,,,,,,,,
mondo:0027676,congenital anomalies of kidney and urinary tract 2,"['congenital anomalies of kidney and urinary tract 2', 'TBX18 congenital anomaly of kidney and urinary tract', 'congenital anomaly of kidney and urinary tract caused by mutation in TBX18', 'hydronephrosis due to Pujo', 'multicystic renal dysplasia, bilateral', 'congenital anomalies of kidney and urinary tract type 2', 'CAKUT2', 'ureteropelvic junction obstruction', 'pelviureteric junction obstruction']",0080207,143400,2190,,,,,,,,,
mondo:0027677,isoniazid toxicity,,,,240887,,,,,,,,,
mondo:0027687,raltegravir toxicity,,,,240905,,,,,,,,,
mondo:0027694,amyotrophic lateral sclerosis type 23,"['ALS23', 'amyotrophic lateral sclerosis 23']",0080225,617839,,CN778765,,,,,,,,
mondo:0027696,voriconazole toxicity,,,,240921,,,,,,,,,
mondo:0027749,serpinopathy,,,,250805,,,,,,,,,
mondo:0027766,generalized lipodystrophy,"['complete generalized lipodystrophy', 'complete generalised lipodystrophy']",0080298,,,C4317112,,C131815,,,,,,0009064
mondo:0027767,partial lipodystrophy,,0080299,,,C4316789,,C131296,,,,,,
mondo:0027772,lung colloid adenocarcinoma,"['lung mucinous cystic tumour of borderline malignancy', 'lung mucinous cystadenocarcinoma', 'mucinous lung adenocarcinoma', 'lung mucinous cystic tumor of borderline malignancy', 'lung colloid adenocarcinoma']",0080304,,,C1708776,,C45512,,,,,,
mondo:0028226,autosomal recessive severe congenital neutropenia,,,,439849,,,C176624,,,,,,
mondo:0028618,gastroenteric neuroendocrine neoplasm,,,,481508,,,,,,,,,
mondo:0029000,poisoning,['Poisonings'],,,,C0302332,,,0008546,D011041,,,,
mondo:0029130,"polydactyly, postaxial, type A8","['polydactyly, postaxial, type A8', 'PAPA8']",,618123,,,"['-0.01135', '0.04797', '0.02129', '-0.02432', '0.05133', '-0.0779', '0.003529', '0.07214', '-0.07135', '-0.0718', '-0.05548', '-0.0221', '-0.010056', '0.02434', '-0.03427', '-0.02945', '0.01409', '-0.06836', '-0.03415', '-0.1404', '0.00577', '-0.0135', '0.0796', '-0.03317', '0.03035', '-0.01139', '-0.02278', '0.00376', '0.03842', '-0.0741', '0.07043', '-0.04013', '0.07983', '0.02988', '0.0694', '-0.05518', '-0.003366', '-0.0392', '-0.02875', '-0.06165', '0.04224', '-0.0402', '0.002592', '0.00694', '0.02155', '-0.0676', '-0.01843', '0.0856', '0.0202', '0.01358', '-0.02893', '-0.01851', '-0.01342', '-0.01276', '-0.055', '-0.0644', '0.02747', '-0.03806', '-0.06744', '0.02313', '0.0362', '0.02112', '0.01395', '0.02219', '-0.0327', '-0.003723', '0.05164', '0.0727', '-0.08966', '0.0645', '-0.0763', '0.03336', '0.06046', '-0.0702', '0.03882', '0.03302', '0.00173', '-0.002268', '-0.08215', '-0.05795', '-0.02988', '-0.006927', '0.008995', '0.0708', '-0.01093', '0.02147', '-0.01502', '0.0853', '0.04776', '0.009445', '0.01507', '0.0671', '0.02995', '0.00922', '0.1631', '0.02834', '0.0686', '-0.1168', '0.01387', '0.067']",,,,,,,
mondo:0029131,"peripheral neuropathy, autosomal recessive, with or without impaired intellectual development","['peripheral neuropathy, autosomal recessive, with or without impaired intellectual development', 'PNRIID']",,618124,,,"['-0.06143', '0.125', '0.06168', '-0.1678', '0.0325', '-0.1442', '-0.0521', '0.2261', '-0.1256', '-0.04095', '-0.0728', '-0.0227', '0.03372', '0.02464', '0.02728', '-0.0466', '0.0136', '-0.1068', '-0.08325', '-0.3357', '-0.02727', '-0.0637', '0.02344', '0.00401', '0.01686', '-0.04193', '-0.03677', '-0.01268', '0.00402', '-0.1318', '0.08936', '-0.0169', '0.1364', '0.0746', '-0.02786', '-0.06885', '-0.0756', '-0.111', '-0.03903', '-0.1786', '0.02022', '-0.144', '0.0711', '0.05157', '-0.0601', '-0.2177', '-0.01512', '0.023', '0.02757', '0.0763', '0.0029', '0.05768', '0.04553', '-0.012634', '-0.01297', '-0.08246', '0.12476', '-0.04077', '-0.2284', '0.05142', '0.06366', '0.04056', '0.09357', '0.06934', '-0.0747', '0.04666', '0.1206', '0.2198', '-0.12305', '0.2043', '-0.1368', '0.03455', '0.02194', '-0.1351', '0.1678', '0.0819', '-0.01127', '0.03644', '-0.08325', '-0.05176', '-0.03656', '-0.0618', '0.03763', '0.2399', '-0.03867', '0.0514', '0.0634', '0.1328', '0.1553', '0.08954', '0.1173', '0.2168', '-0.02477', '0.05496', '0.3252', '0.137', '0.10596', '-0.1879', '-0.02467', '0.1278']",,,,,,,
mondo:0029132,Liddle syndrome 3,"['LIDLS3', 'Liddle syndrome 3']",,618126,,,,,,,,,,
mondo:0029133,"muscular dystrophy, limb-girdle, autosomal dominant 4","['muscular dystrophy, limb-girdle, autosomal dominant 4', 'LGMDD4', 'muscular dystrophy, limb-girdle, type 1I']",,618129,,,"['-0.02534', '0.08875', '0.04102', '-0.0585', '0.128', '-0.2372', '-0.01183', '0.1118', '-0.145', '-0.1514', '-0.02042', '-0.02069', '-0.08453', '0.0653', '0.05334', '-0.0768', '0.03186', '-0.10333', '-0.04855', '-0.217', '-0.0958', '0.005238', '0.03458', '0.05643', '0.009125', '-0.03345', '0.00545', '-0.11383', '-0.0327', '-0.0943', '0.08813', '0.01764', '0.1365', '0.05612', '-0.007244', '0.0098', '0.002274', '-0.0666', '-0.001209', '-0.1152', '0.0012045', '-0.1716', '0.016', '0.01842', '-0.0945', '-0.1059', '-0.0709', '0.11804', '0.00855', '0.03897', '0.04788', '-0.04126', '0.02371', '-0.0083', '-0.0292', '-0.1334', '0.1415', '-0.014', '-0.1272', '0.00391', '0.0653', '-0.03867', '0.0366', '0.06146', '-0.02792', '-0.009254', '0.1569', '0.11414', '-0.09845', '0.03986', '-0.1506', '-0.0674', '0.0275', '-0.05524', '0.1732', '0.06274', '-0.0508', '-0.0653', '-0.09814', '-0.07654', '0.01315', '0.0267', '-0.06226', '0.09576', '-0.007652', '0.0659', '0.04333', '0.1309', '0.0984', '0.1018', '-0.01907', '0.05518', '0.1079', '0.05215', '0.2396', '0.1052', '0.1482', '-0.1332', '-0.0676', '0.04385']",,,,,,,
mondo:0029134,severe combined immunodeficiency due to CARMIL2 deficiency,"['IMD58', 'immunodeficiency 58']",0111984,618131,542301,,"['-0.0392', '0.0504', '0.01269', '-0.0086', '0.02841', '-0.04755', '0.012886', '0.0726', '-0.0409', '-0.05008', '-0.014496', '-0.004593', '-0.003849', '0.0205', '-0.02516', '-0.04565', '-0.00936', '-0.00911', '-0.06232', '-0.1181', '-0.01357', '-0.03583', '0.05624', '-0.02002', '0.01049', '-0.02104', '0.000578', '-0.01581', '-0.005188', '-0.05087', '0.05222', '0.02652', '0.0712', '0.03078', '-0.003489', '-0.03244', '-0.02611', '-0.03375', '-0.00926', '-0.0726', '0.01984', '-0.0609', '0.01616', '-0.02888', '-0.02434', '-0.03513', '0.00125', '0.03047', '0.02295', '0.02928', '-0.01558', '-0.01428', '0.0325', '0.008514', '-0.03418', '-0.008064', '0.04492', '-0.0454', '-0.05914', '0.004635', '0.02808', '0.02513', '0.01431', '0.00909', '0.02055', '0.008415', '0.05865', '0.04465', '-0.0584', '0.05884', '-0.04434', '-0.00227', '-0.00719', '-0.0491', '0.02162', '0.02783', '0.02696', '-0.00733', '-1.323e-05', '-0.01884', '-0.01944', '-0.0002604', '-0.01959', '0.05414', '0.00868', '0.006542', '0.04422', '0.0496', '0.08636', '0.00988', '0.02945', '0.0564', '-0.02469', '0.01029', '0.1326', '0.06555', '0.03848', '-0.0912', '0.006596', '0.02477']",,,,,,,
mondo:0029135,"muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 8","['MDDGC8', 'muscular dystrophy, limb-girdle, autosomal recessive 24', 'Muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT2-related', 'LGMD-POMGNT2 related myopathy', 'muscular dystrophy-dystroglycanopathy (limb-girdle) type C, 8', 'muscular dystrophy-dystroglycanopathy (limb-girdle), TYPE C, 8']",0112382,618135,,,"['-0.01997', '0.1225', '0.05432', '-0.08575', '0.1063', '-0.207', '0.0012455', '0.06744', '-0.22', '-0.05328', '-0.01834', '-0.02106', '-0.02791', '0.03766', '-0.00933', '-0.0886', '-0.00134', '-0.1333', '-0.03622', '-0.1838', '-0.04465', '-0.0645', '0.0975', '0.01075', '0.00667', '-0.06256', '0.013016', '-0.1423', '-0.02797', '-0.1171', '0.1024', '0.0743', '0.201', '0.03766', '0.06006', '-0.06824', '-0.02371', '-0.07245', '-0.0744', '-0.1599', '-0.01546', '-0.212', '-1.19e-05', '0.0695', '-0.1378', '-0.1113', '-0.05975', '0.1627', '-0.01575', '0.08014', '-0.03857', '-0.08514', '0.006435', '-0.001916', '-0.1155', '-0.0455', '0.1494', '-0.0832', '-0.1476', '0.02864', '-0.01392', '-0.004833', '0.04825', '0.06046', '-0.00896', '-0.0381', '0.18', '0.0752', '-0.1126', '0.0323', '-0.12085', '-0.00787', '0.03357', '0.00596', '0.1466', '0.0861', '-0.03784', '-0.04626', '-0.1239', '-0.02269', '0.002993', '-0.0218', '-0.08185', '0.06104', '-0.0283', '0.0553', '0.03345', '0.2123', '0.1777', '0.01775', '-0.00883', '0.0761', '0.08624', '0.033', '0.1775', '0.0962', '0.1515', '-0.1995', '-0.0645', '-0.0361']",,,,,,,
mondo:0029136,"muscular dystrophy, limb-girdle, autosomal recessive 23","['LGMDR23', 'laminin subunit alpha 2-related limb-girdle muscular dystrophy R23', 'muscular dystrophy, limb-girdle, autosomal recessive 23']",,618138,565837,,"['-0.0342', '0.05432', '0.006508', '-0.03073', '0.0509', '-0.12054', '-0.003029', '0.08', '-0.0873', '-0.0722', '-0.005676', '-0.03925', '-0.02759', '0.02675', '0.00641', '-0.01845', '0.01379', '-0.0646', '-0.02884', '-0.1268', '-0.02336', '-0.01452', '0.03424', '0.006', '0.00691', '-0.004333', '-0.00772', '-0.04175', '-0.004166', '-0.04813', '0.05807', '0.02214', '0.0823', '0.03099', '0.005566', '-0.00601', '0.003649', '-0.03247', '0.00483', '-0.09344', '0.02196', '-0.08655', '0.01796', '0.01081', '-0.01657', '-0.06058', '-0.02394', '0.04703', '0.01078', '0.03793', '0.005592', '-0.01545', '0.0213', '0.01642', '-0.0153', '-0.053', '0.0881', '-0.01573', '-0.0721', '-0.001679', '0.04517', '0.004505', '0.01119', '0.01816', '-0.00571', '-0.01614', '0.09094', '0.0578', '-0.0661', '0.0566', '-0.0773', '-0.02942', '0.006233', '-0.01895', '0.0797', '0.03888', '0.00748', '-0.02191', '-0.04843', '-0.02528', '0.013016', '0.002174', '-0.04105', '0.06824', '-0.02438', '0.0325', '0.02148', '0.0727', '0.06506', '0.02052', '0.02158', '0.05002', '0.02419', '0.02415', '0.1436', '0.05515', '0.07684', '-0.07916', '-0.02429', '0.01865']",,,,,,,
mondo:0029137,"hearing loss, autosomal dominant 74","['DFNA74', 'deafness, autosomal dominant 74']",0112165,618140,,,"['-0.01558', '0.08295', '0.03943', '-0.0556', '0.04977', '-0.1382', '0.00739', '0.1398', '-0.07074', '-0.09705', '-0.04544', '-0.03833', '-0.01406', '-0.001399', '-0.005745', '-0.01352', '0.02179', '-0.07654', '-0.04898', '-0.1873', '-0.06073', '-0.03003', '0.0631', '-0.03096', '0.05173', '0.0184', '-0.0469', '-0.04132', '0.0314', '-0.1074', '0.10065', '0.01501', '0.091', '0.0498', '-0.01872', '-0.06256', '-0.02966', '-0.06885', '0.006783', '-0.10394', '0.05356', '-0.1079', '0.06335', '-0.01988', '0.00591', '-0.1675', '-0.05728', '0.08984', '0.03513', '0.0511', '0.04016', '-0.0319', '-0.014786', '-0.02507', '-0.03955', '-0.1141', '0.1351', '-0.03113', '-0.11914', '0.02876', '0.05875', '0.01177', '-0.007187', '0.02554', '-0.02681', '0.031', '0.1073', '0.1113', '-0.10297', '0.1509', '-0.127', '-0.0212', '0.0428', '-0.1051', '0.11664', '0.0657', '0.00397', '-0.02344', '-0.06885', '-0.0457', '0.004986', '-0.001146', '0.004864', '0.1268', '0.001187', '0.03735', '0.05392', '0.11847', '0.0705', '0.0637', '0.0601', '0.1121', '0.01677', '0.01494', '0.2627', '0.05444', '0.1372', '-0.1537', '-0.01361', '0.04596']",,,,,,,
mondo:0029138,"developmental and epileptic encephalopathy, 67","['DEE67', 'EIEE67', 'developmental and epileptic encephalopathy 67', 'epileptic encephalopathy, early infantile, 67']",0112203,618141,,,,,,,,,,
mondo:0029140,glycosylphosphatidylinositol biosynthesis defect 18,"['GPIBD18', 'glycosylphosphatidylinositol biosynthesis defect 18', 'developmental and epileptic encephalopathy 95']",0070382,618143,,,"['-0.09216', '0.03836', '0.009186', '-0.01682', '0.0409', '-0.0991', '-0.01256', '0.07587', '-0.03915', '-0.0405', '-0.02797', '-0.003456', '0.03342', '0.0109', '-0.03162', '-0.0525', '0.01855', '-0.02919', '-0.03244', '-0.129', '-0.004906', '-0.02284', '0.0553', '-0.02313', '0.02965', '-0.01933', '0.003681', '-0.007366', '0.01179', '-0.04324', '0.0685', '0.01659', '0.08966', '0.0425', '0.011566', '-0.03836', '0.0247', '-0.00906', '-0.02899', '-0.0889', '0.0424', '-0.0737', '0.02017', '-0.02213', '-0.01895', '-0.1008', '-0.009155', '0.03433', '0.01646', '0.04553', '-0.02414', '-0.01888', '-0.005493', '0.01282', '-0.0642', '-0.07025', '0.08014', '-0.006985', '-0.0882', '0.01764', '0.04416', '0.02391', '0.0428', '0.01499', '0.02962', '-0.00563', '0.089', '0.04663', '-0.0848', '0.0371', '-0.02756', '0.0397', '0.03062', '-0.02313', '0.03986', '0.06113', '0.01671', '-0.01572', '-0.06555', '-0.0217', '0.01029', '0.00054', '-0.00804', '0.0577', '0.00593', '0.003649', '0.02267', '0.07336', '0.09106', '0.002415', '0.02184', '0.06903', '-0.004425', '-0.01665', '0.1531', '0.0431', '0.073', '-0.1278', '-0.00928', '0.00848']",,,,,,,
mondo:0029141,"Usher syndrome, type 4","['Usher syndrome, type IV', 'USH4']",,618144,,,,,,,,,,
mondo:0029142,"hearing loss, autosomal recessive 111","['DFNB111', 'deafness, autosomal recessive 111']",0111640,618145,,,,,,,,,,
mondo:0029143,intellectual developmental disorder with hypertelorism and distinctive facies,"['INTELLECTUAL DEVELOPMENTAL disorder WITH HYPERTELORISM AND DISTINCTIVE FACIES', 'IDDHDF', 'chromosome 14q32 deletion syndrome']",,618147,,,"['-0.0437', '0.05615', '0.02005', '-0.04996', '0.0337', '-0.06964', '0.00821', '0.0867', '-0.08417', '-0.03111', '-0.01085', '0.0001949', '0.02095', '0.004932', '-0.0392', '-0.014694', '0.01037', '-0.01153', '-0.05475', '-0.1254', '-0.01456', '-0.01802', '0.052', '-0.03123', '0.04013', '-0.02681', '-0.01012', '-0.01007', '0.02313', '-0.02852', '0.04752', '-0.01779', '0.0863', '0.04453', '0.01859', '-0.02692', '-0.03096', '-0.03748', '0.002357', '-0.0719', '0.03265', '-0.0629', '0.00982', '-0.02501', '-0.001306', '-0.05902', '-0.01121', '0.06104', '-0.00198', '0.02516', '-0.0379', '0.002762', '0.007454', '0.00558', '-0.01752', '-0.0238', '0.0363', '-0.02438', '-0.04684', '0.0106', '0.02812', '0.01608', '-0.01822', '0.02917', '0.003906', '0.01293', '0.0495', '0.05408', '-0.05292', '0.07874', '-0.06616', '0.010025', '0.03363', '-0.0238', '-0.004623', '0.02791', '0.0409', '-0.02556', '-0.05246', '-0.04388', '0.005524', '-0.00965', '-0.0363', '0.0887', '-0.002085', '0.0324', '0.008026', '0.0519', '0.0861', '0.02888', '0.00399', '0.07404', '0.00442', '0.03342', '0.1232', '0.01288', '0.05396', '-0.0888', '0.041', '0.03232']",,,,,,,
mondo:0029144,extraoral halitosis due to methanethiol oxidase deficiency,"['EXTRAORAL HALITOSIS DUE TO METHANETHIOL OXIDASE DEFICIENCY', 'extraoral halitosis due to MTO deficiency', 'MTO Deficiency', 'METHANETHIOL Oxidase Deficiency', 'extraoral halitosis with dimethylsulfoxiduria', 'EHMTO']",,618148,,,"['-0.0724', '0.08417', '0.03244', '0.01524', '0.0427', '-0.0883', '0.02188', '0.08185', '-0.04584', '-0.05173', '-0.01724', '-0.01231', '0.004517', '0.01648', '-0.00822', '-0.01698', '-0.03854', '0.0007954', '-0.1023', '-0.1776', '-0.02347', '-0.05038', '0.1105', '-0.03108', '-0.01338', '-0.02385', '-0.01496', '-0.01567', '-0.0006847', '-0.0721', '0.0672', '0.0246', '0.0956', '0.0539', '-0.01402', '-0.07745', '-0.002542', '-0.01953', '-0.01955', '-0.1009', '0.02795', '-0.12366', '0.01984', '-0.003025', '-0.03735', '-0.07117', '0.0357', '0.03357', '0.02307', '0.05002', '-0.02606', '-0.0487', '0.02037', '0.02211', '-0.04877', '-0.0265', '0.0878', '-0.05115', '-0.10455', '0.02924', '0.05075', '0.0336', '0.03705', '-0.01842', '0.02422', '0.01955', '0.0984', '0.0695', '-0.0872', '0.0721', '-0.0731', '-0.00851', '-0.007534', '-0.05673', '0.0584', '0.0836', '0.02884', '-0.01674', '-0.04584', '0.005222', '-0.00756', '-0.004154', '-0.04984', '0.05023', '0.04288', '0.01678', '0.044', '0.0629', '0.1676', '0.01163', '0.05524', '0.06305', '-0.03806', '-0.02657', '0.16', '0.0968', '0.06683', '-0.1382', '-0.00152', '0.04578']",,,,,,,
mondo:0029145,orofacial cleft 8,"['Cleft 51P With or Without Cleft Palate, Nonsyndromic, 8', 'OFC8', 'OROFACIAL CLEFT 8']",0080401,618149,,,,,,,,,,
mondo:0029147,spermatogenic failure 33,"['SPERMATOGENIC FAILURE 33', 'SPGF33']",0111915,618152,,,,,,,,,,
mondo:0029148,spermatogenic failure 34,"['SPERMATOGENIC FAILURE 34', 'SPGF34']",0111911,618153,,,,,,,,,,
mondo:0029465,"intellectual developmental disorder, autosomal dominant 69","['intellectual developmental disorder, autosomal dominant 69', 'mental retardation, autosomal dominant 69', 'MRD69']",,617863,,,,,,,,,,
mondo:0030004,"autism, susceptibility to, 20","['AUTISM, SUSCEPTIBILITY TO, 20', 'autism, susceptibility to, 20', 'AUTS20']",,618830,,,,,,,,,,
mondo:0030005,"epilepsy, early-onset, with or without developmental delay","['EPILEPSY, EARLY-ONSET, WITH OR WITHOUT DEVELOPMENTAL DELAY', 'EPEDD', 'epilepsy, early-onset, with or without developmental delay']",,618832,,,,,,,,,,
mondo:0030006,combined oxidative phosphorylation deficiency 40,"['combined oxidative phosphorylation deficiency 40', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 40', 'COXPD40']",0112117,618835,570491,,,,,,,,,
mondo:0030007,combined oxidative phosphorylation deficiency 41,"['COXPD41', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 41', 'combined oxidative phosphorylation deficiency 41']",0112119,618838,,,,,,,,,,
mondo:0030008,combined oxidative phosphorylation deficiency 42,"['combined oxidative phosphorylation deficiency 42', 'COXPD42', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 42']",0112118,618839,,,,,,,,,,
mondo:0030009,alopecia-intellectual disability syndrome 4,"['alopecia-mental retardation syndrome 4', 'alopecia-intellectual disability syndrome 4', 'APMR4', 'ALOPECIA-MENTAL RETARDATION SYNDROME 4']",0080950,618840,,,,,,,,,,
mondo:0030010,hypogonadotropic hypogonadism 25 with anosmia,"['hypogonadotropic hypogonadism 25 with anosmia', 'HH25', 'HYPOGONADOTROPIC HYPOGONADISM 25 WITH ANOSMIA']",,618841,,,,,,,,,,
mondo:0030012,Diets-Jongmans syndrome,"['DIJOS', 'DIETS-JONGMANS SYNDROME', 'diets-jongmans syndrome', 'Intellectual Developmental Disorder With Distinctive Facial Dysmorphism']",,618846,,,,,,,,,,
mondo:0030013,immunodeficiency 66,"['IMD66', 'IMMUNODEFICIENCY 66', 'immunodeficiency 66']",0111998,618847,,,,,,,,,,
mondo:0030014,"muscular dystrophy, limb-girdle, autosomal recessive 26","['LGMDR26', 'MUSCULAR DYSTROPHY, LIMB-GIRDLE, AUTOSOMAL RECESSIVE 26', 'muscular dystrophy, limb-girdle, autosomal recessive 26']",,618848,,,,,,,,,,
mondo:0030015,bone marrow failure syndrome 6,"['BMFS6', 'BONE MARROW FAILURE SYNDROME 6', 'bone marrow failure syndrome 6']",,618849,,,,,,,,,,
mondo:0030017,combined oxidative phosphorylation deficiency 43,"['combined oxidative phosphorylation deficiency 43', 'COXPD43', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 43']",0112116,618851,,,,,,,,,,
mondo:0030018,autoinflammation with episodic fever and lymphadenopathy,"['Cria Syndrome', 'autoinflammation with episodic fever and lymphadenopathy', 'Cleavage-Resistant Ripk1-Induced Autoinflammatory Syndrome', 'AIEFL', 'AUTOINFLAMMATION WITH EPISODIC FEVER AND LYMPHADENOPATHY']",,618852,,,,,,,,,,
mondo:0030019,anauxetic dysplasia 3,"['ANXD3', 'anauxetic dysplasia 3', 'ANAUXETIC DYSPLASIA 3']",0080963,618853,,,,,,,,,,
mondo:0030020,combined oxidative phosphorylation deficiency 44,"['combined oxidative phosphorylation deficiency 44', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 44', 'COXPD44']",,618855,,,,,,,,,,
mondo:0030024,neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities,"['neurodevelopmental disorder with or without autistic features and/or structural brain abnormalities', 'NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT AUTISTIC FEATURES AND/OR STRUCTURAL BRAIN ABNORMALITIES', 'NEDASB']",,618859,,,,,,,,,,
mondo:0030025,"neurodevelopmental disorder with hypotonia, microcephaly, and seizures","['NEDHYMS', 'neurodevelopmental disorder with hypotonia, microcephaly, and seizures', 'NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, MICROCEPHALY, AND SEIZURES']",,618862,,,,,,,,,,
mondo:0030026,retinal dystrophy with leukodystrophy,"['RDLKD', 'retinal dystrophy with leukodystrophy', 'RETINAL DYSTROPHY WITH LEUKODYSTROPHY']",0080946,618863,,,,,,,,,,
mondo:0030027,"tremor, hereditary essential, 6","['ETM6', 'TREMOR, HEREDITARY ESSENTIAL, 6', 'tremor, hereditary essential, 6']",0081295,618866,,,,,,,,,,
mondo:0030028,"neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline","['NEURODEGENERATION, CHILDHOOD-ONSET, WITH ATAXIA, TREMOR, OPTIC ATROPHY, AND COGNITIVE DECLINE', 'neurodegeneration, childhood-onset, with ataxia, tremor, optic atrophy, and cognitive decline', 'CONATOC']",,618868,,,,,,,,,,
mondo:0030029,"skeletal dysplasia, mild, with joint laxity and advanced bone age","['skeletal dysplasia, mild, with joint laxity and advanced bone age', 'SKELETAL DYSPLASIA, MILD, WITH JOINT LAXITY AND ADVANCED BONE AGE', 'SDJLABA']",,618870,,,,,,,,,,
mondo:0030030,Nizon-Isidor syndrome,"['nizon-isidor syndrome', 'NIZON-ISIDOR SYNDROME', 'NIZIDS']",,618872,,,,,,,,,,
mondo:0030031,lissencephaly 10,"['LIS10', 'lissencephaly 10', 'LISSENCEPHALY 10']",0112229,618873,,,,,,,,,,
mondo:0030033,"seizures, early-onset, with neurodegeneration and brain calcifications","['seizures, early-onset, with neurodegeneration and brain calcifications', 'SEIZURES, EARLY-ONSET, WITH NEURODEGENERATION AND BRAIN CALCIFICATIONS', 'seizures, early-onset, with neurodegeneration and brain calcification', 'SENEBAC']",,618875,,,,,,,,,,
mondo:0030034,"epilepsy, progressive myoclonic, 11","['EPILEPSY, PROGRESSIVE MYOCLONIC, 11', 'EPM11', 'epilepsy, progressive myoclonic, 11']",,618876,,,,,,,,,,
mondo:0030035,"leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome","['leukoencephalopathy, developmental delay, and episodic neurologic regression syndrome', 'LEUKOENCEPHALOPATHY, DEVELOPMENTAL DELAY, AND EPISODIC NEUROLOGIC REGRESSION SYNDROME', 'Leuden Syndrome', 'LEUDEN']",,618877,,,,,,,,,,
mondo:0030036,"leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome","['leukoencephalopathy, motor delay, spasticity, and dysarthria syndrome', 'Lemspad Syndrome', 'LEMSPAD', 'LEUKOENCEPHALOPATHY, MOTOR DELAY, SPASTICITY, AND DYSARTHRIA SYNDROME']",,618878,,,,,,,,,,
mondo:0030037,"neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures","['Glycosylphosphatidylinositol Biosynthesis Defect 22', 'NEDHCAS', 'NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND CEREBELLAR ATROPHY, WITH OR WITHOUT SEIZURES', 'neurodevelopmental disorder with hypotonia and cerebellar atrophy, with or without seizures']",,618879,,,,,,,,,,
mondo:0030038,"glaucoma, primary closed-angle","['glaucoma, primary closed-angle', 'GLAUCOMA, PRIMARY CLOSED-ANGLE', 'GLCC']",,618880,,,,,,,,,,
mondo:0030042,"proteinuria, chronic benign","['proteinuria, chronic benign', 'PROCHOB', 'PROTEINURIA, CHRONIC BENIGN']",,618884,,,,,,,,,,
mondo:0030043,"congenital disorder of glycosylation, type iit","['Cdg Iit', 'CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIt', 'CDG2T']",,618885,,,,,,,,,,
mondo:0030044,pseudo-TORCH syndrome 3,"['PSEUDO-TORCH SYNDROME 3', 'pseudo-torch syndrome 3', 'PTORCH3']",,618886,,,,,,,,,,
mondo:0030045,Liberfarb syndrome,"['LIBF', 'Liberfarb syndrome', 'spondyloepimetaphyseal dysplasia, Liberfarb Type', 'short stature-skeletal dysplasia-retinal degeneration-intellectual disability-sensorineural hearing loss syndrome']",,618889,589442,,,,,,,,,
mondo:0030046,neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity,"['NEURODEVELOPMENTAL DISORDER AND STRUCTURAL BRAIN ANOMALIES WITH OR WITHOUT SEIZURES AND SPASTICITY', 'neurodevelopmental disorder and structural brain anomalies with or without seizures and spasticity', 'NEDBASS']",,618890,,,,,,,,,,
mondo:0030047,"microcephaly, developmental delay, and brittle hair syndrome","['MDBH', 'MICROCEPHALY, DEVELOPMENTAL DELAY, AND BRITTLE HAIR SYNDROME', 'microcephaly, developmental delay, and brittle hair syndrome']",,618891,,,,,,,,,,
mondo:0030048,harderoporphyria,"['HARDEROPORPHYRIA', 'HARPO', 'harderoporphyria']",,618892,,,,,,C562816,,,,
mondo:0030049,"46,xx sex reversal 5","['46,xx sex reversal 5', 'SRXX5', '46,XX SEX REVERSAL 5']",0080943,618901,,,,,,,,,,
mondo:0030051,"intellectual developmental disorder with autistic features and language delay, with or without seizures","['intellectual developmental disorder with autistic features and language delay, with or without seizures', 'INTELLECTUAL DEVELOPMENTAL DISORDER WITH AUTISTIC FEATURES AND LANGUAGE DELAY, WITH OR WITHOUT SEIZURES', 'IDDALDS']",,618906,,,,,,,,,,
mondo:0030054,"developmental and epileptic encephalopathy, 86","['developmental and epileptic encephalopathy 86', 'DEE86', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 86', 'EIEE86', 'epileptic encephalopathy, early infantile, 86']",0112220,618910,,,,,,,,,,
mondo:0030055,sorbitol dehydrogenase deficiency with peripheral neuropathy,"['SORBITOL DEHYDROGENASE DEFICIENCY WITH PERIPHERAL NEUROPATHY', 'SORDD', 'Sorbitol Dehydrogenase Deficiency', 'sorbitol dehydrogenase deficiency with peripheral neuropathy']",,618912,,,,,,,,,,
mondo:0030056,Fanconi renotubular syndrome 5,"['Fanconi Renotubular Syndrome, Acadian Variant', 'Fanconi renotubular syndrome 5', 'FANCONI RENOTUBULAR SYNDROME 5', 'FRTS5']",0080761,618913,,,,,,,,,,
mondo:0030057,"neurodevelopmental, jaw, eye, and digital syndrome","['NEDJED', 'neurodevelopmental, jaw, eye, and digital syndrome', 'NEURODEVELOPMENTAL, JAW, EYE, AND DIGITAL SYNDROME']",,618914,,,,,,,,,,
mondo:0030058,"hearing loss, autosomal dominant 77","['DFNA77', 'deafness, autosomal dominant 77']",0112168,618915,,,,,,,,,,
mondo:0030059,"developmental and epileptic encephalopathy, 87","['EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 87', 'DEE87', 'developmental and epileptic encephalopathy 87', 'EIEE87', 'epileptic encephalopathy, early infantile, 87']",0112221,618916,,,,,,,,,,
mondo:0030060,neurodevelopmental disorder with language impairment and behavioral abnormalities,"['NEURODEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND BEHAVIORAL ABNORMALITIES', 'NEDLIB', 'neurodevelopmental disorder with language impairment and behavioral abnormalities']",,618917,,,,,,,,,,
mondo:0030061,periventricular nodular heterotopia 9,"['PERIVENTRICULAR NODULAR HETEROTOPIA 9', 'PVNH9', 'periventricular nodular heterotopia 9']",,618918,,,,,,,,,,
mondo:0030062,"arrhythmogenic right ventricular dysplasia, familial, 14","['ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 14', 'Arrhythmogenic Right Ventricular Cardiomyopathy 14', 'ARVD14', 'arrhythmogenic right ventricular dysplasia, familial, 14']",0080959,618920,,,,,,,,,,
mondo:0030063,"neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities","['NEDSHBA', 'neurodevelopmental disorder with seizures, hypotonia, and brain imaging abnormalities', 'NEURODEVELOPMENTAL DISORDER WITH SEIZURES, HYPOTONIA, AND BRAIN IMAGING ABNORMALITIES', 'neurodevelopmental disorder with seizures, hypotonia, and brain abnormalities']",,618922,,,,,,,,,,
mondo:0030064,"episodic ataxia, type 9","['EA9', 'EPISODIC ATAXIA, TYPE 9', 'episodic ataxia, type 9']",,618924,,,,,,,,,,
mondo:0030065,"agenesis of corpus callosum, cardiac, ocular, and genital syndrome","['ACOGS', 'AGENESIS OF CORPUS CALLOSUM, CARDIAC, OCULAR, AND GENITAL SYNDROME', 'agenesis of corpus callosum, cardiac, ocular, and genital syndrome']",0080948,618929,,,,,,,,,,
mondo:0030066,"granulomatous disease, chronic, autosomal recessive, 5","['chronic granulomatous disease 5, autosomal recessive', 'granulomatous disease, chronic, autosomal recessive, 5', 'Granulomatous Disease, Chronic, Due to Cybc1 Deficiency', 'CGD5', 'GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL RECESSIVE, 5']",0070368,618935,,,,,,,,,,
mondo:0030067,Treacher Collins syndrome 4,"['TREACHER COLLINS SYNDROME 4', 'Treacher-Collins syndrome 4', 'TCS4', 'treacher collins syndrome 4']",0080792,618939,,,,,,,,,,
mondo:0030069,"hyper-IgE recurrent infection syndrome 5, autosomal recessive","['HIES5', 'hyper-IgE recurrent infection syndrome 5, autosomal recessive', 'HYPER-IgE RECURRENT INFECTION SYNDROME 5, AUTOSOMAL RECESSIVE']",,618944,,,,,,,,,,
mondo:0030070,"heterotaxy, visceral, 9, autosomal, with male infertility","['HTX9', 'HETEROTAXY, VISCERAL, 9, AUTOSOMAL, WITH MALE INFERTILITY', 'heterotaxy, visceral, 9, autosomal, with male infertility']",,618948,,,,,,,,,,
mondo:0030071,retinitis pigmentosa 89,"['RETINITIS PIGMENTOSA 89', 'RP89', 'retinitis pigmentosa 89']",0112146,618955,,,,,,,,,,
mondo:0030072,"developmental and epileptic encephalopathy, 88","['DEE88', 'developmental and epileptic encephalopathy 88', 'epileptic encephalopathy, early infantile, 88', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 88', 'EIEE88']",0112222,618959,,,,,,,,,,
mondo:0030073,Mitchell syndrome,"['Mitchell syndrome', 'MITCH', 'ACOX1 dysregulation']",,618960,631248,,,,,,,,,
mondo:0030074,spondylometaphyseal dysplasia with corneal dystrophy,"['spondylometaphyseal dysplasia with corneal dystrophy', 'SMDCD', 'SPONDYLOMETAPHYSEAL DYSPLASIA WITH CORNEAL DYSTROPHY']",0112303,618961,589435,,,,,,,,,
mondo:0030077,"vertebral, cardiac, renal, and limb defects syndrome 3","['vertebral, cardiac, renal, and limb defects syndrome 3', 'Congenital Nad Deficiency Disorder 3', 'VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 3', 'VCRL3']",,618845,,,,,,,,,,
mondo:0030087,"diabetes mellitus, permanent neonatal 2","['diabetes mellitus, permanent neonatal 2', 'DIABETES MELLITUS, PERMANENT NEONATAL 2', 'PNDM2', 'Developmental Delay, Epilepsy, and Neonatal Diabetes 1', 'diabetes, permanent neonatal 2, with or without neurologic features']",,618856,,,,,,,,,,
mondo:0030088,"diabetes mellitus, permanent neonatal 3","['diabetes mellitus, permanent neonatal 3', 'diabetes mellitus, permanent neonatal 3, with or without neurologic features', 'DIABETES MELLITUS, PERMANENT NEONATAL 3', 'Developmental Delay, Epilepsy, and Neonatal Diabetes 2', 'PNDM3']",,618857,,,,,,,,,,
mondo:0030089,"diabetes mellitus, permanent neonatal 4","['PNDM4', 'diabetes mellitus, permanent neonatal 4', 'DIABETES MELLITUS, PERMANENT NEONATAL 4']",,618858,,,,,,,,,,
mondo:0030105,galactosemia 4,"['Galactose Mutarotase Deficiency', 'GALAC4', 'GALM mutarotase deficiency', 'GALACTOSEMIA IV', 'galactosemia iv']",,618881,570422,,,,,,,,,
mondo:0030116,silver-russell syndrome 2,"['SILVER-RUSSELL SYNDROME 2', 'Uniparental Disomy, Maternal, Chromosome 7', 'silver-russell syndrome 2', 'SRS2']",,618905,,,,,,,,,,
mondo:0030118,silver-russell syndrome 4,"['silver-russell syndrome 4', 'SILVER-RUSSELL SYNDROME 4', 'SRS4']",,618907,,,,,,,,,,
mondo:0030134,oculopharyngodistal myopathy 2,"['oculopharyngodistal myopathy 2', 'OCULOPHARYNGODISTAL MYOPATHY 2', 'OPDM2']",0081298,618940,,,,,,,,,,
mondo:0030258,"pontocerebellar hypoplasia, type 14","['pontocerebellar hypoplasia, type 14', 'PCH14']",0112325,619301,613274,,,,,,,,,
mondo:0030259,"pontocerebellar hypoplasia, type 15","['pontocerebellar hypoplasia, type 15', 'PCH15']",0112326,619302,,,,,,,,,,
mondo:0030260,"pontocerebellar hypoplasia, type 1E","['pontocerebellar hypoplasia, type 1E', 'PCH1E']",0112330,619303,,,,,,,,,,
mondo:0030261,"pontocerebellar hypoplasia, type 1F","['PCH1F', 'pontocerebellar hypoplasia, type 1F']",0112331,619304,,,,,,,,,,
mondo:0030263,"leukodystrophy, hypomyelinating, 21","['HLD21', 'leukodystrophy, hypomyelinating, 21']",0070407,619310,,,,,,,,,,
mondo:0030266,immunodeficiency 80 with or without congenital cardiomyopathy,"['immunodeficiency 80 with or without congenital cardiomyopathy', 'immunodeficiency 80 with or without cardiomyopathy', 'IMD80', 'immunodeficiency with or without congenital cardiomyopathy', 'MCM10 deficiency']",,619313,,,,,,,,,,
mondo:0030268,developmental and epileptic encephalopathy 6B,"['DEE6B', 'developmental and epileptic encephalopathy 6B', 'developmental and epileptic encephalopathy 6B, non-Dravet']",0070379,619317,,,,,,,,,,
mondo:0030270,lymphatic malformation 9,"['LMPHM9', 'lymphatic malformation 9']",,619319,,,,,,,,,,
mondo:0030281,arthrogryposis multiplex congenita 6,"['arthrogryposis multiplex congenita 6', 'AMC6']",0070336,619334,,,,,,,,,,
mondo:0030293,"angioedema, hereditary, 5","['HAE5', 'angioedema, hereditary, 5']",,619361,,,,,,,,,,
mondo:0030294,megacystis-microcolon-intestinal hypoperistalsis syndrome 3,"['megacystis-microcolon-intestinal hypoperistalsis syndrome 3', 'MMIHS3']",,619362,,,,,,,,,,
mondo:0030296,megacystis-microcolon-intestinal hypoperistalsis syndrome 4,"['megacystis-microcolon-intestinal hypoperistalsis syndrome 4', 'MMIHS4']",,619365,,,,,,,,,,
mondo:0030298,"angioedema, hereditary, 8","['angioedema, hereditary, 8', 'HAE8']",,619367,,,,,,,,,,
mondo:0030300,"cardiomyopathy, dilated, 2D","['CMD2D', 'cardiomyopathy, dilated, 2D']",0081160,619371,,,,,,,,,,
mondo:0030302,immunodeficiency 81,"['IMD81', 'T-B+ severe combined immunodeficiency\xa0due to SLP76 deficiency', 'immunodeficiency 81']",,619374,,,,,,,,,,
mondo:0030307,spermatogenic failure 55,"['spermatogenic failure 55', 'SPGF55']",0112337,619380,,,,,,,,,,
mondo:0030308,immunodeficiency 82 with systemic inflammation,"['IMD82', 'immunodeficiency with systemic inflammation', 'immunodeficiency 82 with systemic inflammation']",,619381,,,,,,,,,,
mondo:0030309,"Leber hereditary optic neuropathy, autosomal recessive","['LHONAR', 'mitochondrial complex 1 deficiency, nuclear type 38', 'Leber hereditary optic neuropathy, autosomal recessive']",,619382,,,,,,,,,,
mondo:0030311,combined oxidative phosphorylation deficiency 52,"['COXPD52', 'combined oxidative phosphorylation deficiency 52']",,619386,,,,,,,,,,
mondo:0030312,"spinocerebellar ataxia, autosomal recessive 29","['spinocerebellar ataxia, autosomal recessive 29', 'SCAR29', 'neurodevelopmental disorder with hypotonia and cerebellar ataxia', 'Barakat-Van Ham-Kaya syndrome']",0070410,619389,,,,,,,,,,
mondo:0030313,"encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10","['encephalopathy, acute, infection-induced (herpes-specific), susceptibility to, 10', 'herpes simplex encephalitis, susceptibility to, 7', 'IIAE10']",,619396,,,,,,,,,,
mondo:0030314,"inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive","['inflammatory bowel disease (infantile ulcerative colitis) 31, autosomal recessive', 'inflammatory bowel disease, early-onset, autosomal recessive', 'inflammatory bowel disease (infantile ulcerative colitis) 31', 'IBD31']",,619398,,,,,,,,,,
mondo:0030316,lymphatic malformation 11,"['LMPHM11', 'lymphatic malformation 11']",,619401,,,,,,,,,,
mondo:0030317,"cardiomyopathy, familial hypertrophic, 28","['CMH28', 'cardiomyopathy, familial hypertrophic, 28']",,619402,,,,,,,,,,
mondo:0030318,"spinocerebellar ataxia, autosomal recessive 30","['SCAR30', 'spinocerebellar ataxia, autosomal recessive 30']",0070411,619405,,,,,,,,,,
mondo:0030323,"spinocerebellar ataxia, autosomal recessive 31","['spinocerebellar ataxia, autosomal recessive 31', 'SCAR31']",0070412,619422,,,,,,,,,,
mondo:0030326,mitochondrial dna depletion syndrome 16B (neuroophthalmic type),"['mitochondrial dna depletion syndrome 16B (neuroophthalmic type)', 'MTDPS16B']",,619425,,,,,,,,,,
mondo:0030329,megacystis-microcolon-intestinal hypoperistalsis syndrome 5,"['megacystis-microcolon-intestinal hypoperistalsis syndrome 5', 'MMIHS5']",,619431,,,,,,,,,,
mondo:0030330,"cardiomyopathy, familial restrictive, 6","['cardiomyopathy, familial restrictive, 6', 'RCM6']",,619433,,,,,,,,,,
mondo:0030331,Ritscher-Schinzel syndrome 4,"['Ritscher-Schinzel syndrome 4', 'RTSC4']",,619435,,,,,,,,,,
mondo:0030332,"ciliary dyskinesia, primary, 46","['ciliary dyskinesia, primary, 46', 'CILD46']",,619436,,,,,,,,,,
mondo:0030333,immunodeficiency 84,"['IMD84', 'immunodeficiency due to IKZF3 deficiency', 'immunodeficiency 84']",,619437,,,,,,,,,,
mondo:0030334,"encephalitis, acute, infection (viral)-induced, susceptibility to, 11","['IIAE11', 'encephalitis, acute, infection (viral)-induced, susceptibility to, 11']",,619441,,,,,,,,,,
mondo:0030335,"diarrhea 12, with microvillus atrophy","['DIAR12', 'diarrhea 12, with microvillus atrophy', 'microvillus inclusion disease 2']",,619445,,,,,,,,,,
mondo:0030337,"cutis laxa, autosomal recessive, type 2E","['ARCL2E', 'cutis laxa, autosomal recessive, type 2E', 'cutis laxa, autosomal recessive, type IIE']",,619451,,,,,,,,,,
mondo:0030338,anencephaly 2,"['ANPH2', 'anencephaly 2']",,619452,,,,,,,,,,
mondo:0030339,"microcephaly 28, primary, autosomal recessive","['microcephaly 28, primary, autosomal recessive', 'MCPH28']",,619453,,,,,,,,,,
mondo:0030341,"myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive","['CMS7B', 'myasthenic syndrome, congenital, 7B, presynaptic, autosomal recessive']",,619461,,,,,,,,,,
mondo:0030346,"ciliary dyskinesia, primary, 47, and lissencephaly","['CILD47', 'ciliary dyskinesia, primary, 47, and lissencephaly']",,619466,,,,,,,,,,
mondo:0030353,Joubert syndrome 38,"['JBTS38', 'Joubert syndrome 38']",,619476,,,,,,,,,,
mondo:0030354,"facioscapulohumeral muscular dystrophy 3, digenic","['facioscapulohumeral muscular dystrophy 3, digenic', 'FSHD3']",,619477,,,,,,,,,,
mondo:0030355,"facioscapulohumeral muscular dystrophy 4, digenic","['facioscapulohumeral muscular dystrophy 4, digenic', 'facioscapulohumeral muscular dystrophy 4, digenic, digenic dominant', 'FSHD4']",,619478,,,,,,,,,,
mondo:0030356,short-rib thoracic dysplasia 21 without polydactyly,"['SRTD21', 'short-rib thoracic dysplasia 21 without polydactyly']",,619479,,,,,,,,,,
mondo:0030360,"cholestasis, progressive familial intrahepatic, 6","['PFIC6', 'cholestasis, progressive familial intrahepatic, 6']",,619484,,,,,,,,,,
mondo:0030361,Aicardi-Goutieres syndrome 8,"['AGS8', 'Aicardi-Goutieres syndrome 8']",,619486,,,,,,,,,,
mondo:0030362,Aicardi-Goutieres syndrome 9,"['Aicardi-Goutieres syndrome 9', 'AGS9']",,619487,,,,,,,,,,
mondo:0030366,"cardiomyopathy, dilated, 2E","['cardiomyopathy, dilated, 2E', 'CMD2E']",0081161,619492,,,,,,,,,,
mondo:0030374,WHIM syndrome 2,['WHIMS2'],,619407,,,,,,,,,,
mondo:0030375,"neurologic, endocrine, and pancreatic disease, multisystem, infantile-onset 2",['IMNEPD2'],,619418,,,,,,,,,,
mondo:0030376,Martsolf syndrome 2,['MARTS2'],,619420,,,,,,,,,,
mondo:0030378,combined oxidative phosphorylation deficiency 53,"['COXPD53', 'combined oxidative phosphorylation deficiency due to C2orf69 deficiency']",,619423,,,,,,,,,,
mondo:0030397,"portal hypertension, noncirrhotic, 2",['NCPH2'],,619463,,,,,,,,,,
mondo:0030399,"visceral neuropathy, familial, 2, autosomal recessive",['VSCN2'],,619465,,,,,,,,,,
mondo:0030423,"congenital disorder of glycosylation, type 2v",['CDG2V'],,619493,,,,,,,,,,
mondo:0030428,immunodeficiency 85 and autoimmunity,['IMD85'],,619510,,,,,,,,,,
mondo:0030430,spermatogenic failure 56,['SPGF56'],0112336,619515,,,,,,,,,,
mondo:0030433,"Charcot-Marie-Tooth disease, axonal, type 2FF","['CMT2FF', 'Charcot-Marie-Tooth neuropathy']",,619519,,,,,,,,,,
mondo:0030434,"epilepsy, idiopathic generalized, susceptibility to, 18",['EIG18'],,619521,,,,,,,,,,
mondo:0030436,"anemia, sideroblastic, 5",['SIDBA5'],,619523,,,,,,,,,,
mondo:0030437,"congenital disorder of glycosylation, type IIw",['CDG2W'],,619525,,,,,,,,,,
mondo:0030438,"pontocerebellar hypoplasia, type 16",['PCH16'],0112333,619527,,,,,,,,,,
mondo:0030439,spermatogenic failure 57,['SPGF57'],0112338,619528,,,,,,,,,,
mondo:0030440,cone-rod dystrophy 22,['CORD22'],,619531,,,,,,,,,,
mondo:0030448,immunodeficiency 86,['IMD86'],,619549,,,,,,,,,,
mondo:0030449,"hearing loss, autosomal recessive 118, with cochlear aplasia","['deafness, autosomal recessive 118, with cochlear aplasia', 'DFNB118']",,619553,,,,,,,,,,
mondo:0030453,developmental and epileptic encephalopathy 97,['DEE97'],0070383,619561,,,,,,,,,,
mondo:0030454,Joubert syndrome 39,['JBTS39'],,619562,,,,,,,,,,
mondo:0030455,dystonia 31,['DYT31'],,619565,,,,,,,,,,
mondo:0030456,"muscular dystrophy, limb-girdle, autosomal recessive 27",['LGMDR27'],,619566,,,,,,,,,,
mondo:0030457,immunodeficiency 87 and autoimmunity,"['immunodeficiency due to DEF6 deficiency', 'IMD87']",,619573,,,,,,,,,,
mondo:0030458,"Charcot-Marie-Tooth disease, axonal, Type 2HH",['CMT2HH'],,619574,,,,,,,,,,
mondo:0030462,Joubert syndrome 40,['JBTS40'],,619582,,,,,,,,,,
mondo:0030463,spermatogenic failure 58,['SPGF58'],0112352,619585,,,,,,,,,,
mondo:0030465,cataract 49,['CTRCT49'],,619593,,,,,,,,,,
mondo:0030471,Galloway-Mowat syndrome 9,['GAMOS9'],,619603,,,,,,,,,,
mondo:0030472,developmental and epileptic encephalopathy 98,['DEE98'],0070384,619605,,,,,,,,,,
mondo:0030473,developmental and epileptic encephalopathy 99,['DEE99'],0070385,619606,,,,,,,,,,
mondo:0030474,"heterotaxy, visceral, 10, autosomal, with male infertility",['HTX10'],,619607,,,,,,,,,,
mondo:0030475,"heterotaxy, visceral, 11, autosomal, with male infertility",['HTX11'],,619608,,,,,,,,,,
mondo:0030476,Galloway-Mowat syndrome 10,['GAMOS10'],,619609,,,,,,,,,,
mondo:0030480,"hearing loss, autosomal recessive 119","['deafness, autosomal recessive 119', 'DFNB119']",,619615,,,,,,,,,,
mondo:0030482,"spastic paraplegia 84, autosomal recessive",['SPG84'],0112347,619621,,,,,,,,,,
mondo:0030483,immunodeficiency 88,"['Mendelian susceptibility to mycobacterial diseases due to TBX21 deficiency', 'IMD88']",,619630,,,,,,,,,,
mondo:0030484,immunodeficiency 89 and autoimmunity,['IMD89'],,619632,,,,,,,,,,
mondo:0030486,dystonia 32,['DYT32'],,619637,,,,,,,,,,
mondo:0030487,"spondylometaphyseal dysplasia, pagnamenta type",['SMDP'],,619638,,,,,,,,,,
mondo:0030489,"epidermolysis bullosa simplex 2A, generalized severe",['EBS2A'],,619555,,,,,,,,,,
mondo:0030490,oocyte maturation defect 11,['OOMD11'],,619643,,,,,,,,,,
mondo:0030491,immunodeficiency 91 and hyperinflammation,"['IMD91', 'immunodeficiency, autosomal recessive, due to ZNFX1 deficiency:']",,619644,,,,,,,,,,
mondo:0030492,spermatogenic failure 59,['SPGF59'],0112357,619645,,,,,,,,,,
mondo:0030493,spermatogenic failure 60,['SPGF60'],0112355,619646,,,,,,,,,,
mondo:0030498,immunodeficiency 92,"['immunodeficiency due to REL deficiency', 'IMD92']",,619652,,,,,,,,,,
mondo:0030500,Loeys-Dietz syndrome 6,['LDS6'],,619656,,,,,,,,,,
mondo:0030502,tetrasomy,,,,,,,C36601,1001297,D058670,,,,
mondo:0030503,"cholestasis, progressive familial intrahepatic, 7, with or without hearing loss",['PFIC7'],,619658,,,,,,,,,,
mondo:0030505,"cholestasis, progressive familial intrahepatic, 8",['PFIC8'],,619662,,,,,,,,,,
mondo:0030506,ovarian dysgenesis 9,['ODG9'],,619665,,,,,,,,,,
mondo:0030507,spermatogenic failure 61,['SPGF61'],0112350,619672,,,,,,,,,,
mondo:0030508,spermatogenic failure 62,['SPGF62'],0112351,619673,,,,,,,,,,
mondo:0030512,"spastic paraplegia 85, autosomal recessive",['SPG85'],0112345,619686,,,,,,,,,,
mondo:0030513,dystonia 33,['DYT33'],,619687,,,,,,,,,,
mondo:0030514,"leukodystrophy, hypomyelinating, 23, with ataxia, deafness, liver dysfunction, and dilated cardiomyopathy",['HLD23'],0070397,619688,,,,,,,,,,
mondo:0030515,spermatogenic failure 63,['SPGF63'],0112356,619689,,,,,,,,,,
mondo:0030517,"trichothiodystrophy 8, nonphotosensitive",['TTD8'],,619691,,,,,,,,,,
mondo:0030518,"trichothiodystrophy 9, nonphotosensitive",['TTD9'],,619692,,,,,,,,,,
mondo:0030519,"agammaglobulinemia 9, autosomal recessive",['AGM9'],0081141,619693,,,,,,,,,,
mondo:0030522,spermatogenic failure 64,['SPGF64'],0112353,619696,,,,,,,,,,
mondo:0030523,oocyte maturation defect 12,['OOMD12'],,619697,,,,,,,,,,
mondo:0030524,"mucopolysaccharidosis, type 10",['MPS10'],,619698,,,,,,,,,,
mondo:0030525,"epidermolysis bullosa simplex 2B, generalized intermediate",['EBS2B'],,619588,,,,,,,,,,
mondo:0030527,"epidermolysis bullosa simplex 2C, localized",['EBS2C'],,619594,,,,,,,,,,
mondo:0030528,immunodeficiency 93 and hypertrophic cardiomyopathy,"['immunodeficiency and hypertrophic cardiomyopathy', 'IMD93']",,619705,,,,,,,,,,
mondo:0030529,"agammaglobulinemia 10, autosomal dominant",['AGM10'],0081142,619707,,,,,,,,,,
mondo:0030531,spermatogenic failure 65,['SPGF65'],0112354,619712,,,,,,,,,,
mondo:0030533,"intellectual developmental disorder, autosomal recessive 73",['MRT73'],0081233,619717,,,,,,,,,,
mondo:0030534,hypogonadotropic hypogonadism 26 with or without anosmia,['HH26'],,619718,,,,,,,,,,
mondo:0030535,"epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive",['EBS2D'],,619599,,,,,,,,,,
mondo:0030537,"central hypoventilation syndrome, congenital, 2, and autonomic dysfunction","['central hypoventilation syndrome, congenital, 2, and autonomic dysfunction', 'CCHS2']",,619482,,,,,,,,,,
mondo:0030538,"dystonia 34, myoclonic",['DYT34'],,619724,,,,,,,,,,
mondo:0030539,"central hypoventilation syndrome, congenital, 3","['CCHS3', 'central hypoventilation syndrome, congenital, 3']",,619483,,,,,,,,,,
mondo:0030543,combined oxidative phosphorylation deficiency 54,['COXPD54'],,619737,,,,,,,,,,
mondo:0030549,"hearing loss, autosomal dominant 81","['deafness, autosomal dominant 81', 'hearing loss, autosomal dominant 81', 'DFNA81']",,619500,,,,,,,,,,
mondo:0030553,acromesomelic dysplasia 4,['AMD4'],0081238,619636,,,,,,,,,,
mondo:0030602,Klebsiella pneumonia,"['Klebsiella caused pneumonia', 'pneumonia due to Klebsiella pneumoniae']",13272,,,C0519030,,,,D007710,482.0,J15.0,,
mondo:0030603,Klebsiella infectious disease,"['Klebsiella caused disease or disorder', 'infections, Klebsiella', 'Klebsiella infection', 'infection, Klebsiella']",,,,,,,1001353,D007710,,,,
mondo:0030604,cystic partially differentiated nephroblastoma,"['cystic partially differentiated nephroblastoma', 'malignant cystic nephroma', 'malignant multilocular cystic nephroma']",7571,,,C1266139,,C6897,,,,,,
mondo:0030606,Bryant-Li-Bhoj neurodevelopmental syndrome 1,['BRYLIB1'],,619720,,,,,,,,,,
mondo:0030607,Bryant-Li-Bhoj neurodevelopmental syndrome 2,['BRYLIB2'],,619721,,,,,,,,,,
mondo:0030608,interstitial lung disease 1,"['ILD1', 'interstitial lung disease 1']",,619611,,,,,,,,,,
mondo:0030619,retinitis pigmentosa 92,"['RP92', 'retinitis pigmentosa 92']",,619614,,,,,,,,,,
mondo:0030625,"dyskinesia with orofacial involvement, autosomal recessive","['DSKOR', 'dyskinesia with orofacial involvement, autosomal recessive']",,619647,,,,,,,,,,
mondo:0030634,"leukoencephalopathy, hereditary diffuse, with spheroids 2","['leukoencephalopathy, hereditary diffuse, with spheroids, swedish IIA', 'leukoencephalopathy, hereditary diffuse, with spheroids 2', 'HDLS2']",,619661,,,,,,,,,,
mondo:0030639,Teebi hypertelorism syndrome,,0081073,,,,,,,,,,,
mondo:0030669,gastrointestinal defects and immunodeficiency syndrome 2,"['GIDID2', 'multiple intestinal atresia with or without leukopenia', 'gastrointestinal defects and immunodeficiency syndrome 2']",,619708,,,,,,,,,,
mondo:0030673,"spastic paraplegia 86, autosomal recessive","['SPG86', 'spastic paraplegia 86, autosomal recessive']",0112342,619735,,,,,,,,,,
mondo:0030674,Teebi hypertelorism syndrome 2,"['TBHS2', 'Teebi hypertelorism syndrome 2']",0081074,619736,,,,,,,,,,
mondo:0030676,"parkinsonism-dystonia 3, childhood-onset","['parkinsonism-dystonia 3, childhood-onset', 'PKDYS3']",,619738,,,,,,,,,,
mondo:0030677,"Charcot-Marie-Tooth disease, demyelinating, IIA 1I","['Charcot-Marie-Tooth disease, demyelinating, IIA 1I', 'Charcot-Marie-Tooth disease neuropathy, IIA 1I', 'CMT1I']",,619742,,,,,,,,,,
mondo:0030679,Noonan syndrome 14,"['NS14', 'Noonan syndrome 14']",,619745,,,,,,,,,,
mondo:0030680,"cardiomyopathy, dilated, 2F","['cardiomyopathy, dilated, 2F', 'CMD2F']",0081162,619747,,,,,,,,,,
mondo:0030681,immunodeficiency 94 with autoinflammation and dysmorphic facies,"['IMD94', 'immunodeficiency 94 with autoinflammation and dysmorphic facies']",,619750,,,,,,,,,,
mondo:0030684,hypogonadotropic hypogonadism 27 without anosmia,"['hypogonadotropic hypogonadism 27 without anosmia', 'HH27']",,619755,,,,,,,,,,
mondo:0030689,"Charcot-Marie-Tooth disease, demyelinating, IIA 1H","['neuropathy, hereditary, with or without age-related macular degeneration', 'CMT1H', 'Charcot-Marie-Tooth neuropathy, IIA 1H', 'Charcot-Marie-Tooth disease, demyelinating, IIA 1H', 'hereditary motor and sensory neuropathy, 1h']",,619764,,,,,,,,,,
mondo:0030690,"pulmonary fibrosis and/or bone marrow failure, telomere-related, 6","['PFBMFT6', 'pulmonary fibrosis and/or bone marrow failure, telomere-related, 6']",,619767,,,,,,,,,,
mondo:0030692,immunodeficiency 95,"['immunodeficiency 95', 'IMD95']",,619773,,,,,,,,,,
mondo:0030693,immunodeficiency 96,"['immunodeficiency, autosomal recessive due to LIG1 deficiency', 'IMD96', 'immunodeficiency 96']",,619774,,,,,,,,,,
mondo:0030695,developmental and epileptic encephalopathy 100,"['DEE100', 'developmental and epileptic encephalopathy 100']",0070386,619777,,,,,,,,,,
mondo:0030696,mitochondrial DNA depletion syndrome 20 (mngie type),"['MTDPS20', 'mitochondrial neurogastrointestinal encephalomyopathy syndrome, lig3-related', 'mitochondrial DNA depletion syndrome 20 (mngie type)']",,619780,,,,,,,,,,
mondo:0030697,"myopia 28, autosomal recessive","['myopia 28, autosomal recessive', 'MYP28']",,619781,,,,,,,,,,
mondo:0030700,autoimmune glomerulonephritis,,0040094,,,,,,,,,,,
mondo:0030701,autoimmune cardiomyopathy,,0040095,,,,,,,,,,,
mondo:0030702,autoimmune atherosclerosis,,0040096,,,,,,,,,,,
mondo:0030703,autoimmune vasculitis,,0040097,,,C1328843,,,,,,,,
mondo:0030705,Trichomonas prostatitis,"['Trichomonas prostatitis', 'Trichomonas vaginalis caused prostatitis (disease)']",,,,C0153315,,C35176,,,131.03,,,
mondo:0030706,Trichomonas cystitis,"['Trichomonas vaginalis caused cystitis', 'Trichomonas cystitis']",,,,C0341733,,C35405,,,131.09,,,
mondo:0030707,Trichomonas balanoposthitis,['Trichomonas balanoposthitis'],,,,C0341769,,C35406,,,,,,
mondo:0030708,Trichomonas cervicitis,"['Trichomonas cervicitis', 'Trichomonas vaginalis caused cervicitis (disease)']",,,,,,C35588,,,,,,
mondo:0030711,"Anemia, congenital dyserythropoietic, type IIIb, autosomal recessive","['CDAN3B', 'anemia, congenital dyserythropoietic, IIA IIIB, autosomal recessive', 'CDA, IIA IIIB']",,619789,,,,,,,,,,
mondo:0030712,oculopharyngodistal myopathy 4,"['oculopharyngodistal myopathy 4', 'OPDM4']",0081300,619790,,,,,,,,,,
mondo:0030714,"osteogenesis imperfecta, IIA 22","['osteogenesis imperfecta, IIA 22', 'OI22']",,619795,,,,,,,,,,
mondo:0030716,spermatogenic failure 66,"['SPGF66', 'spermatogenic failure 66']",,619799,,,,,,,,,,
mondo:0030717,immunodeficiency 97 with autoinflammation,"['IMD97', 'immunodeficiency 97 with autoinflammation']",,619802,,,,,,,,,,
mondo:0030718,spermatogenic failure 67,"['SPGF67', 'spermatogenic failure 67']",,619803,,,,,,,,,,
mondo:0030719,"hearing loss, autosomal dominant 82","['deafness, autosomal dominant 82', 'DFNA82']",,619804,,,,,,,,,,
mondo:0030720,trichomonal vulvovaginitis,['Trichomonas vaginalis caused vulvovaginitis'],,,,C2945558,,,,,131.01,,,
mondo:0030721,spermatogenic failure 68,"['SPGF68', 'spermatogenic failure 68']",,619805,,,,,,,,,,
mondo:0030723,"hearing loss, autosomal dominant 83","['DFNA83', 'deafness, autosomal dominant 83']",,619808,,,,,,,,,,
mondo:0030724,"hearing loss, autosomal dominant 84","['DFNA84', 'deafness, autosomal dominant 84']",,619810,,,,,,,,,,
mondo:0030726,"neutropenia, severe congenital, 9, autosomal dominant","['neutropenia, severe congenital, 9, autosomal dominant', 'SCN9']",,619813,,,,,,,,,,
mondo:0030727,developmental and epileptic encephalopathy 101,"['developmental and epileptic encephalopathy 101', 'DEE101']",0070387,619814,,,,,,,,,,
mondo:0030729,Tessadori-van Haaften neurodevelopmental syndrome 1,"['TEVANED1', 'Tessadori-van Haaften neurodevelopmental syndrome 1']",,619758,,,,,,,,,,
mondo:0030730,Tessadori-van Haaften neurodevelopmental syndrome 2,"['TEVANED2', 'Tessadori-van Haaften neurodevelopmental syndrome 2']",,619759,,,,,,,,,,
mondo:0030731,"aortic aneurysm, familial thoracic 12","['AAT12', 'aortic aneurysm, familial thoracic 12']",,619825,,,,,,,,,,
mondo:0030732,spermatogenic failure 69,"['spermatogenic failure 69', 'SPGF69']",,619826,,,,,,,,,,
mondo:0030733,spermatogenic failure 70,"['SPGF70', 'spermatogenic failure 70']",,619828,,,,,,,,,,
mondo:0030736,ovarian dysgenesis 10,"['ODG10', 'ovarian dysgenesis 10']",,619834,,,,,,,,,,
mondo:0030746,"epidermolysis bullosa, junctional 2A, intermediate","['epidermolysis bullosa, junctional 2A, non-herlitz IIA', 'epidermolysis bullosa, junctional 2A, intermediate', 'epidermolysis bullosa, junctional 2A, generalized intermediate', 'epidermolysis bullosa, junctional 2A, generalised intermediate', 'JEB2A']",,619783,,,,,,,,,,
mondo:0030747,"epidermolysis bullosa, junctional 2B, severe","['epidermolysis bullosa, junctional 2B, severe', 'epidermolysis bullosa, junctional 2B, herlitz IIA', 'JEB2B', 'epidermolysis bullosa, junctional 2B, generalised severe', 'epidermolysis bullosa, junctional 2B, generalized severe']",,619784,,,,,,,,,,
mondo:0030748,"epidermolysis bullosa, junctional 3A, intermediate","['JEB3A', 'epidermolysis bullosa, junctional 3A, generalized intermediate', 'epidermolysis bullosa, junctional 3A, non-herlitz IIA', 'epidermolysis bullosa, junctional 3A, generalised intermediate', 'epidermolysis bullosa, junctional 3A, intermediate']",,619785,,,,,,,,,,
mondo:0030749,"epidermolysis bullosa, junctional 3B, severe","['JEB3B', 'epidermolysis bullosa, junctional 3B, severe', 'epidermolysis bullosa, junctional 3B, herlitz IIA', 'epidermolysis bullosa, junctional 3B, generalized severe', 'epidermolysis bullosa, junctional 3B, generalised severe']",,619786,,,,,,,,,,
mondo:0030750,"epidermolysis bullosa, junctional 4, intermediate","['epidermolysis bullosa, generalized atrophic benign', 'epidermolysis bullosa, junctional 4, intermediate', 'JEB4', 'epidermolysis bullosa, junctional 4, non-herlitz IIA', 'epidermolysis bullosa, generalised atrophic benign', 'epidermolysis bullosa, junctional, localisata variant']",,619787,,,,,,,,,,
mondo:0030756,Stuve-Wiedemann syndrome 2,"['Stuve-Wiedemann syndrome 2', 'STWS2']",,619751,,,,,,,,,,
mondo:0030768,"epidermolysis bullosa, junctional 5A, intermediate","['epidermolysis bullosa, junctional 5A, intermediate', 'JEB5A', 'epidermolysis bullosa, junctional 5A, generalised intermediate', 'epidermolysis bullosa, junctional 5A, generalized intermediate', 'epidermolysis bullosa, junctional 5A, non-herlitz IIA']",,619816,,,,,,,,,,
mondo:0030770,congenital disorder of deglycosylation 2,"['congenital disorder of deglycosylation 2', 'CDDG2']",,619775,,,,,,,,,,
mondo:0030781,restrictive dermopathy 2,"['restrictive dermopathy 2', 'RSDM2', 'restrictive dermopathy 2, lethal']",0070370,619793,,,,,,,,,,
mondo:0030785,"intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly","['MRT75', 'intellectual developmental disorder, autosomal recessive 75, with neuropsychiatric features and variant lissencephaly']",0081234,619827,,,,,,,,,,
mondo:0030787,spermatogenic failure 71,"['SPGF71', 'spermatogenic failure 71']",,619831,,,,,,,,,,
mondo:0030796,"leukoencephalopathy, hereditary diffuse, with spheroids",,,,,,,,,,,,,
mondo:0030797,retinitis pigmentosa 93,"['retinitis pigmentosa 93', 'RP93']",,619845,,,,,,,,,,
mondo:0030798,immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias,"['immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias', 'IMD99']",,619846,,,,,,,,,,
mondo:0030800,"cholestasis, progressive familial intrahepatic, 9","['PFIC9', 'cholestasis, progressive familial intrahepatic, 9']",,619849,,,,,,,,,,
mondo:0030801,monosomy 7 myelodysplasia and leukemia syndrome 2,"['monosomy 7 myelodysplasia and leukemia syndrome 2', 'M7MLS2']",,619041,,,,,,,,,,
mondo:0030805,spinocerebellar ataxia 49,"['spinocerebellar ataxia 49', 'SCA49']",,619806,631106,,,,,,,,,
mondo:0030809,spermatogenic failure 72,"['SPGF72', 'spermatogenic failure 72']",,619867,,,,,,,,,,
mondo:0030810,"cholestasis, progressive familial intrahepatic, 10","['PFIC10', 'cholestasis, progressive familial intrahepatic, 10']",,619868,,,,,,,,,,
mondo:0030813,immunodeficiency 101 (varicella zoster virus-specific),"['IMD101', 'immunodeficiency 101 (varicella zoster virus-specific)']",,619872,,,,,,,,,,
mondo:0030815,"cholestasis, progressive familial intrahepatic, 11","['PFIC11', 'cholestasis, progressive familial intrahepatic, 11']",,619874,,,,,,,,,,
mondo:0030818,spermatogenic failure 73,"['spermatogenic failure 73', 'SPGF73']",,619878,,,,,,,,,,
mondo:0030819,meckel syndrome 14,"['MKS14', 'meckel syndrome 14']",,619879,,,,,,,,,,
mondo:0030822,renal hypodysplasia/aplasia 4,"['renal hypodysplasia/aplasia 4', 'RHDA4']",,619887,,,,,,,,,,
mondo:0030827,"macrothrombocytopenia, isolated, 2, autosomal dominant","['macrothrombocytopenia, isolated, 2, autosomal dominant', 'MACTHC2']",,619840,,,,,,,,,,
mondo:0030831,gastrointestinal defect and immunodeficiency syndrome,,,,,,,,,,,,,
mondo:0030835,"developmental delay, impaired growth, dysmorphic facies, and axonal neuropathy",['DIGFAN'],,619090,,,,,,,,,,
mondo:0030837,"neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities","['NEDMILEG', 'neurodevelopmental disorder with microcephaly, impaired language, epilepsy, and gait abnormalities, autosomal dominant', 'NEDMILEG, AD']",,619092,,,,,,,,,,
mondo:0030839,"thyroid hormone metabolism, abnormal, 2","['thyroid hormone metabolism, abnormal, 2', 'THMA2']",,619855,,,,,,,,,,
mondo:0030840,mismatch repair cancer syndrome 2,"['mismatch repair cancer syndrome 2', 'MMRCS2']",,619096,,,,,,,,,,
mondo:0030841,mismatch repair cancer syndrome 3,"['MMRCS3', 'mismatch repair cancer syndrome 3']",,619097,,,,,,,,,,
mondo:0030843,mismatch repair cancer syndrome 4,"['MMRCS4', 'mismatch repair cancer syndrome 4']",,619101,,,,,,,,,,
mondo:0030844,spermatogenic failure 47,"['SPGF47', 'spermatogenic failure 47']",0112175,619102,,,,,,,,,,
mondo:0030846,spermatogenic failure 48,"['SPGF48', 'spermatogenic failure 48']",0112176,619108,,,,,,,,,,
mondo:0030847,"arthrogryposis, distal, type 1C","['DA1C', 'arthrogryposis, distal, type 1C']",0112190,619110,,,,,,,,,,
mondo:0030849,intellectual developmental disorder with speech delay and axonal peripheral neuropathy,['IDDSAPN'],,619099,,,,,,,,,,
mondo:0030852,"neurodevelopmental disorder with dysmorphic facies, sleep disturbance, and brain abnormalities","['neurodevelopmental disorder wtih dysmorphic facies, sleep disturbance, and brain abnormalities', 'NEDFASB']",,619103,,,,,,,,,,
mondo:0030854,combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1,"['combined osteogenesis imperfecta and Ehlers-Danlos syndrome 1', 'OIEDS1', 'OIEDS Syndrome 1']",,619115,,,,,,,,,,
mondo:0030855,combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2,"['combined osteogenesis imperfecta and Ehlers-Danlos syndrome 2', 'OIEDS2', 'OIEDS Syndrome 2']",,619120,,,,,,,,,,
mondo:0030856,developmental and epileptic encephalopathy 89,"['developmental and epileptic encephalopathy 89', 'DEE89']",0112223,619124,,,,,,,,,,
mondo:0030858,immunodeficiency 75,"['IMD75', 'immunodeficiency 75']",,619126,,,,,,,,,,
mondo:0030859,COACH syndrome 2,['COACH2'],,619111,,,,,,,,,,
mondo:0030860,"neuronopathy, distal hereditary motor, type 5C","['spinal muscular atrophy, distal, type 5C', 'HMN5C', 'DHMN5C', 'neuropathy, distal hereditary motor, type VC']",,619112,,,,,,,,,,
mondo:0030861,"osteogenesis imperfecta, type 21","['OI21', 'osteogenesis imperfecta 21', 'osteogenesis imperfecta, TYPE XXI']",0112201,619131,,,,,,,,,,
mondo:0030862,COACH syndrome 3,['COACH3'],,619113,,,,,,,,,,
mondo:0030864,Ritscher-Schinzel syndrome 3,"['RTSC3', 'Ritscher-Schinzel syndrome 3']",,619135,,,,,,,,,,
mondo:0030866,"neurodevelopmental disorder with cardiomyopathy, spasticity, and brain abnormalities",['NEDCASB'],,619121,,,,,,,,,,
mondo:0030867,thrombocytopenia 7,"['Thrombocytopenia, Autosomal Dominant, 7', 'THC7', 'thrombocytopenia 7']",,619130,,,,,,,,,,
mondo:0030868,spermatogenic failure 49,"['spermatogenic failure 49', 'SPGF49']",0112271,619144,,,,,,,,,,
mondo:0030869,spermatogenic failures 50,"['spermatogenic failure', 'spermatogenic failures 50', 'SPGF50']",0112272,619145,,,,,,,,,,
mondo:0030870,premature ovarian failure 17,"['premature ovarian failure 17', 'POF17']",0080874,619146,,,,,,,,,,
mondo:0030871,vertebral hypersegmentation and orofacial anomalies,['VHO'],0070418,619122,,,,,,,,,,
mondo:0030872,frontotemporal dementia and/or amyotrophic lateral sclerosis 8,"['FTDALS8', 'frontotemporal dementia and/or amyotrophic lateral sclerosis 8']",,619132,,,,,,,,,,
mondo:0030873,cardiofacioneurodevelopmental syndrome,['CFNDS'],,619123,,,,,,,,,,
mondo:0030875,frontotemporal dementia and/or amyotrophic lateral sclerosis 5,"['frontotemporal dementia and/or amyotrophic lateral sclerosis 5', 'FTDALS5']",,619141,,,,,,,,,,
mondo:0030876,cardioacrofacial dysplasia 1,"['cardioacrofacial dysplasia 1', 'CAFD1']",,619142,,,,,,,,,,
mondo:0030877,cardioacrofacial dysplasia 2,"['CAFD2', 'cardioacrofacial dysplasia 2, autosomal dominant, somatic mosaicism', 'cardioacrofacial dysplasia 2']",,619143,,,,,,,,,,
mondo:0030878,Kaya-Barakat-Masson syndrome,['KABAMAS'],,619125,,,,,,,,,,
mondo:0030880,mandibuloacral dysplasia progeroid syndrome,"['mandibuloacral dysplasia associated to MTX2', 'MDPS']",,619127,,,,,,,,,,
mondo:0030881,developmental and epileptic encephalopathy 102,"['DEE102', 'developmental and epileptic encephalopathy 102']",0070388,619881,,,,,,,,,,
mondo:0030883,carpal tunnel syndrome 2,"['carpal tunnel syndrome 2', 'CTS2']",,619161,,,,,,,,,,
mondo:0030885,amyotrophic lateral sclerosis 26 with or without frontotemporal dementia,['ALS26'],,619133,,,,,,,,,,
mondo:0030886,holoprosencephaly 14,"['HPE14', 'holoprosencephaly 14']",,619895,,,,,,,,,,
mondo:0030887,"cardiomyopathy, dilated, 2G","['CMD2G', 'cardiomyopathy, dilated, 2G']",0081163,619897,,,,,,,,,,
mondo:0030890,"pontocerebellar hypoplasia, IIA 17","['PCH17', 'pontocerebellar hypoplasia, IIA 17']",,619909,,,,,,,,,,
mondo:0030891,"intellectual developmental disorder, autosomal dominant 66","['intellectual developmental disorder, autosomal dominant 66', 'MRD66', 'mental retardation, autosomal dominant 66']",,619910,,,,,,,,,,
mondo:0030893,"leukoencephalopathy, progressive, infantile-onset, with or without deafness",['LEPID'],,619147,,,,,,,,,,
mondo:0030894,"AMED syndrome, digenic","['AMeD syndrome', 'bone marrow failure syndrome 7, digenic', 'AMEDS', 'AMED syndrome, digenic', 'aplastic anemia-intellectual disability-dwarfism syndrome']",0080952,619151,611216,,,,,,,,,
mondo:0030895,"nephrotic syndrome, type 22","['NPHS22', 'nephrotic syndrome, type 22']",0112268,619155,,,,,,,,,,
mondo:0030896,chromosome 13q33-q34 deletion syndrome,,,619148,,,,,,,,,,
mondo:0030897,Lessel-Kreienkamp syndrome,['LESKRES'],,619149,,,,,,,,,,
mondo:0030898,immunodeficiency 76,"['combined immunodeficiency due to FCHO1 deficiency', 'immunodeficiency 76', 'IMD76', 'immunodeficiency due to FCHO1 deficiency']",,619164,647804,,,,,,,,,
mondo:0030899,oculocutaneous albinism type 8,"['oculocutaneous albinism, type 8', 'oculocutaneous albinism, type VIII', 'OCA8']",,619165,597733,,,,,,,,,
mondo:0030900,intellectual developmental disorder with paroxysmal dyskinesia or seizures,['IDDPADS'],,619150,,,,,,,,,,
mondo:0030902,"mitochondrial complex 1 deficiency, nuclear type 36","['mitochondrial complex 1 deficiency, nuclear type 36', 'MC1DN36', 'mitochondrial complex I deficiency, nuclear type 36']",,619170,,,,,,,,,,
mondo:0030903,Hermansky-Pudlak syndrome 11,"['HPS11', 'Hermansky-Pudlak syndrome']",,619172,,,,,,,,,,
mondo:0030905,"hearing loss, autosomal recessive 117","['deafness, autosomal recessive 117', 'DFNB117']",,619174,,,,,,,,,,
mondo:0030906,Trichomonas tenax infectious disease,"['Trichomonas tenax trichomoniasis', 'Trichomonas tenax caused disease or disorder']",0050270,,,,,,,,,,,
mondo:0030907,"intellectual disability, X-linked 106","['X-linked mental retardation 106', 'intellectual disability, X-linked 106', 'X-linked intellectual disability 106', 'intellectual developmental disorder, X-linked 106, X-linked recessive', 'mental retardation, X-linked 106', 'MRX106']",0080240,300997,,,,,,,,,,
mondo:0030908,"intellectual disability, X-linked, syndromic, 35","['syndromic X-linked mental retardation 35', 'MRXS35', 'intellectual disability, X-linked, syndromic, 35', 'syndromic X-linked intellectual disability 35', 'intellectual developmental disorder, X-linked, syndromic, 35, X-linked recessive', 'mental retardation, X-linked, syndromic, 35']",0080241,300998,459070,,,,,,,,,
mondo:0030909,"intellectual disability, X-linked, syndromic, Houge type","['intellectual disability, X-linked, syndromic, Houge type', 'mental retardation, X-linked, syndromic, Houge type', 'syndromic X-linked intellectual disability Hough type', 'intellectual developmental disorder, X-linked, syndromic, Houge type', 'mental retardation, X-linked, syndromic, HOUGE type', 'syndromic X-linked mental retardation Hough type', 'intellectual disability, X-linked, syndromic, HOUGE type', 'MRXSHG']",0080242,301008,442835,CN679647,,,,,,,,
mondo:0030910,"intellectual disability, autosomal dominant 45","['mental retardation, autosomal dominant 45', 'autosomal dominant mental retardation 45', 'autosomal dominant intellectual disability 45', 'MRD45', 'intellectual disability, autosomal dominant 45']",0080236,617600,,CN368509,,,,,,,,
mondo:0030911,"intellectual disability, autosomal dominant 46","['mental retardation, autosomal dominant 46', 'autosomal dominant mental retardation 46', 'intellectual disability, autosomal dominant 46', 'MRD46', 'autosomal dominant intellectual disability 46']",0080237,617601,,CN371052,,,,,,,,
mondo:0030912,"intellectual disability, autosomal dominant 47","['mental retardation, autosomal dominant 47', 'intellectual disability, autosomal dominant 47', 'autosomal dominant mental retardation 47', 'STAG1-related intellectual disability-facial dysmorphism-gastroesophageal reflux syndrome', 'MRD47', 'autosomal dominant intellectual disability 47']",0080238,617635,502434,CN429988,,,,,,,,
mondo:0030913,"intellectual disability, autosomal dominant 48","['microcephaly-corpus callosum and cerebellar vermis hypoplasia-facial dysmorphism-intellectual disability syndrom', 'autosomal dominant intellectual disability 48', 'intellectual disability, autosomal dominant 48', 'autosomal dominant mental retardation 48', 'mental retardation, autosomal dominant 48', 'MRD48']",0080235,617751,500159,CN580791,"['-0.01834', '0.1498', '0.5254', '-0.3752', '0.0899', '-0.1804', '-0.00574', '0.3574', '-0.583', '-0.356', '-0.0812', '-0.271', '0.0865', '-0.4014', '0.01678', '-0.01622', '0.1112', '-0.236', '-0.1483', '-0.3015', '0.2255', '0.2042', '0.0274', '-0.3994', '0.2446', '-0.4373', '-0.2249', '0.1304', '0.3906', '-0.05783', '0.1498', '-0.2399', '0.4702', '0.2477', '0.1733', '-0.05032', '-0.431', '-0.1696', '-0.10114', '-0.419', '0.3696', '-0.2903', '-0.1333', '-0.07544', '-0.03955', '-0.6504', '0.1256', '0.3745', '-0.1869', '-0.12177', '-0.1311', '0.2333', '-0.404', '-0.1979', '-0.0481', '-0.02092', '-0.1724', '0.0111', '-0.281', '0.07306', '-0.012', '0.0752', '-0.3958', '0.1366', '-0.2249', '-0.01863', '0.353', '0.2737', '-0.2494', '0.3726', '-0.3901', '0.4214', '-0.00815', '-0.0869', '-0.4153', '0.1774', '0.411', '-0.273', '-0.0912', '0.049', '-0.11035', '0.083', '0.003407', '0.5635', '0.02765', '0.07526', '-0.1792', '0.3767', '0.2037', '0.2776', '0.1742', '0.631', '0.2478', '0.1978', '0.6045', '0.3625', '0.3203', '-0.00875', '0.5273', '0.3408']",,0009156,,,,,
mondo:0030914,Clark-Baraitser syndrome,"['Clark-Baraitser syndrome', 'Baraitser syndrome', 'intellectual disability, tall stature, obesity, macrocephaly and typical facial features', 'autosomal dominant intellectual disability 49', 'intellectual disability, autosomal dominant 49', 'autosomal dominant mental retardation 49', 'MRD49', 'mental retardation, tall stature, obesity, macrocephaly and typical facial features', 'mental retardation, autosomal dominant 49']",0080234,617752,600731,CN593636,"['-0.02158', '0.0784', '0.03354', '-0.0894', '0.05103', '-0.1674', '-0.006844', '0.1381', '-0.10187', '-0.11536', '-0.03937', '-0.00414', '0.01836', '-0.01439', '0.02463', '-0.00993', '0.01631', '-0.0534', '-0.05185', '-0.2275', '-0.03128', '0.00997', '0.0395', '-0.03998', '0.06158', '-0.00433', '-0.04767', '-0.03363', '0.01111', '-0.0853', '0.1075', '-0.02042', '0.1141', '0.05338', '-0.006153', '-0.07434', '-0.04193', '-0.0835', '-0.00762', '-0.103', '0.0759', '-0.1259', '0.02512', '-0.011765', '-0.0439', '-0.1595', '-0.03586', '0.06665', '0.013145', '0.01027', '0.00341', '-0.02202', '-0.01449', '-0.0469', '-0.02089', '-0.06216', '0.10333', '-0.00637', '-0.1178', '0.0503', '0.06445', '0.007698', '0.03928', '0.01205', '-0.00932', '0.03766', '0.0723', '0.11884', '-0.1068', '0.1086', '-0.1051', '-0.01507', '0.0275', '-0.1045', '0.0867', '0.0742', '0.02914', '-0.01456', '-0.05713', '-0.03323', '-0.02005', '0.00822', '-0.02058', '0.1544', '0.0169', '0.0787', '0.02692', '0.11426', '0.11505', '0.12274', '0.02518', '0.1344', '0.000941', '0.00625', '0.2664', '0.0744', '0.10333', '-0.1488', '0.03864', '0.0732']",,,C536208,,,,
mondo:0030915,"intellectual disability, autosomal recessive 61","['Alwadei syndrome', 'autosomal recessive mental retardation 61', 'intellectual disability, autosomal recessive 61', 'MRT61', 'mental retardation, autosomal recessive 61', 'autosomal recessive intellectual disability 61']",0080239,617773,,CN651335,,,,,,,,
mondo:0030916,"intellectual disability, autosomal dominant 50","['mental retardation, autosomal dominant 50', 'intellectual disability, autosomal dominant 50', 'intellectual developmental disorder, autosomal dominant 50, with behavioural abnormalities', 'autosomal dominant mental retardation 50', 'MRD50', 'autosomal dominant intellectual disability 50', 'intellectual developmental disorder, autosomal dominant 50, with behavioral abnormalities']",0080233,617787,,CN671930,"['-0.010345', '0.0574', '0.01996', '-0.05267', '0.03268', '-0.1078', '0.006042', '0.115', '-0.07214', '-0.0643', '-0.03009', '-0.01418', '0.01765', '0.00852', '0.0117', '-0.03787', '-0.00469', '-0.02882', '-0.02917', '-0.1548', '-0.01677', '0.0001234', '0.03513', '-0.03137', '0.03717', '-0.02554', '-0.03053', '-0.02705', '0.01291', '-0.05893', '0.07153', '-0.02258', '0.0933', '0.02263', '0.002613', '-0.0307', '-0.02493', '-0.0536', '0.00849', '-0.05902', '0.05154', '-0.07196', '0.014275', '-0.0314', '0.001802', '-0.0845', '-0.02219', '0.04346', '0.01085', '0.0336', '-0.0106', '0.00976', '-0.008', '-0.03168', '-0.01602', '-0.03107', '0.04993', '-0.01674', '-0.08264', '0.0212', '0.04965', '0.01956', '0.02644', '-0.00759', '0.01866', '0.02176', '0.05634', '0.09863', '-0.0877', '0.0823', '-0.06635', '0.005814', '0.004547', '-0.0738', '0.0706', '0.04742', '0.00673', '-0.010704', '-0.06305', '-0.02368', '-0.0282', '-0.01157', '-0.01674', '0.0762', '0.00671', '0.03702', '0.02682', '0.0776', '0.0931', '0.05435', '0.03165', '0.0718', '-0.0258', '0.004692', '0.1813', '0.03894', '0.0732', '-0.105', '0.01648', '0.0504']",,,,,,,
mondo:0030917,"intellectual disability, autosomal dominant 51","['autosomal dominant intellectual disability 51', 'intellectual disability, autosomal dominant 51', 'mental retardation, autosomal dominant 51', 'MRD51', 'autosomal dominant mental retardation 51']",0080232,617788,,CN671931,"['0.006153', '0.08405', '0.013435', '-0.07874', '0.07715', '-0.1708', '0.007996', '0.1619', '-0.0874', '-0.0898', '-0.05618', '0.01456', '0.001798', '0.009575', '0.02423', '-0.0427', '-0.02116', '-0.05865', '-0.06097', '-0.2302', '-0.05167', '-0.012566', '0.03934', '-0.0319', '0.05762', '0.0001568', '-0.0679', '-0.05786', '0.005688', '-0.1037', '0.0878', '-0.02211', '0.1167', '0.0378', '-0.00604', '-0.06168', '-0.0458', '-0.093', '0.00587', '-0.0976', '0.0713', '-0.1498', '0.03906', '-0.000667', '-0.01274', '-0.1522', '-0.04993', '0.08655', '0.00432', '0.0492', '-0.013725', '0.00932', '-0.004757', '-0.04785', '-0.0209', '-0.06134', '0.10596', '-0.003351', '-0.11145', '0.02151', '0.0717', '0.01336', '0.01362', '0.01104', '-0.02179', '0.0126', '0.0891', '0.123', '-0.0751', '0.0837', '-0.0823', '-0.0354', '0.03427', '-0.10425', '0.0639', '0.07715', '-0.008156', '-0.05005', '-0.0602', '-0.046', '-0.0185', '-0.01846', '-0.026', '0.1464', '0.03062', '0.07733', '0.03864', '0.09204', '0.1458', '0.0952', '0.03915', '0.1292', '-0.013275', '0.01463', '0.2625', '0.0823', '0.1293', '-0.1378', '0.03296', '0.04855']",,,,,,,
mondo:0030918,"intellectual disability, autosomal dominant 52","['autosomal dominant mental retardation 52', 'MRD52', 'autosomal dominant intellectual disability 52', 'intellectual disability, autosomal dominant 52', 'mental retardation, autosomal dominant 52']",0080231,617796,,CN671932,"['-0.06494', '0.1002', '0.04037', '-0.09607', '0.0638', '-0.1735', '-0.01974', '0.1381', '-0.1326', '-0.1101', '-0.06976', '0.00752', '0.003561', '-0.002193', '-0.01636', '0.00764', '0.03958', '-0.05743', '-0.07806', '-0.2283', '-0.0576', '-0.0257', '0.0651', '-0.0726', '0.045', '0.02171', '-0.03284', '-0.03888', '0.035', '-0.10614', '0.0942', '0.00252', '0.1293', '0.03983', '-0.0336', '-0.04184', '-0.05228', '-0.0895', '-0.001536', '-0.10266', '0.03174', '-0.1377', '0.039', '-0.02338', '-0.02008', '-0.1923', '-0.0426', '0.07935', '0.01065', '0.00684', '0.00862', '0.01825', '-0.03394', '-0.059', '-0.02328', '-0.1576', '0.13', '-0.02663', '-0.1646', '0.04605', '0.0712', '-0.01813', '0.01793', '0.02686', '0.01863', '-0.002638', '0.1305', '0.1272', '-0.143', '0.1188', '-0.1753', '-0.02718', '0.067', '-0.1371', '0.06155', '0.07684', '0.03723', '-0.0386', '-0.076', '-0.04486', '0.01979', '0.0159', '-0.03387', '0.1289', '0.01441', '0.0438', '0.06247', '0.1561', '0.1282', '0.08167', '0.0402', '0.1284', '-0.001511', '0.03946', '0.2612', '0.0945', '0.1473', '-0.1854', '0.0625', '0.0673']",,0009152,,,,,
mondo:0030919,"intellectual disability, autosomal dominant 53","['intellectual disability, autosomal dominant 53', 'autosomal dominant intellectual disability 53', 'mental retardation, autosomal dominant 53', 'autosomal dominant mental retardation 53', 'MRD53']",0080228,617798,,,"['-0.0784', '0.1026', '0.07587', '-0.1056', '0.03537', '-0.1848', '-0.0279', '0.1514', '-0.1127', '-0.1097', '-0.0752', '-0.006386', '0.0146', '-0.01196', '0.01278', '-0.01007', '0.02994', '-0.06247', '-0.0782', '-0.2202', '-0.05347', '-0.00845', '0.03195', '-0.1136', '0.01886', '-0.002619', '-0.05264', '-0.0779', '0.04742', '-0.137', '0.1036', '-0.01065', '0.1354', '0.01485', '-0.01451', '-0.0452', '-0.05817', '-0.0827', '-0.0193', '-0.1299', '0.0721', '-0.1595', '0.02795', '-0.03024', '-0.0213', '-0.2064', '-0.05374', '0.0675', '0.01399', '0.02747', '0.00714', '0.0351', '-0.06155', '-0.0444', '-0.01973', '-0.1243', '0.1395', '-0.0444', '-0.1904', '0.073', '0.05682', '0.002214', '0.02873', '0.02844', '0.00801', '0.01527', '0.1451', '0.1261', '-0.1865', '0.141', '-0.1755', '-0.000268', '0.05588', '-0.12006', '0.11194', '0.07513', '0.03098', '-0.03078', '-0.092', '-0.04117', '0.04425', '0.010025', '-0.002369', '0.1699', '0.02074', '0.01814', '0.0626', '0.1716', '0.1312', '0.06354', '0.06052', '0.1527', '-0.01209', '0.03748', '0.2854', '0.0829', '0.1649', '-0.1823', '0.0612', '0.07776']",,0009165,,,,,
mondo:0030920,"intellectual disability, autosomal dominant 54","['autosomal dominant mental retardation 54', 'autosomal dominant intellectual disability 54', 'MRD54', 'mental retardation, autosomal dominant 54', 'intellectual disability, autosomal dominant 54']",0080230,617799,,,"['-0.0708', '0.1562', '0.038', '-0.09625', '0.04636', '-0.1892', '-0.04907', '0.1865', '-0.10297', '-0.11487', '-0.06995', '0.0324', '-0.002325', '-0.002348', '0.00856', '-0.03152', '0.02138', '-0.0684', '-0.08136', '-0.1858', '-0.06168', '-0.00929', '0.02696', '-0.09436', '0.06537', '-0.002079', '-0.04233', '-0.04535', '0.01611', '-0.1222', '0.0885', '-0.008804', '0.1332', '0.02875', '-0.0263', '-0.0577', '-0.0537', '-0.1172', '-0.01086', '-0.12366', '0.04907', '-0.1375', '0.04404', '-0.05505', '-0.03284', '-0.1854', '-0.05704', '0.09534', '0.01926', '0.007267', '0.0375', '0.001532', '-0.0456', '-0.04013', '-0.01608', '-0.1637', '0.1776', '-0.0078', '-0.2056', '0.04846', '0.0684', '-0.009445', '-0.01124', '0.03885', '-0.01393', '-0.008545', '0.152', '0.10645', '-0.1678', '0.1329', '-0.09625', '0.00712', '0.0699', '-0.1721', '0.09503', '0.0794', '0.0194', '-0.01625', '-0.08307', '-0.02528', '0.04572', '0.0289', '-0.02643', '0.1411', '0.01704', '0.01799', '0.0738', '0.1954', '0.1206', '0.09735', '0.032', '0.1365', '-0.01675', '0.04257', '0.2805', '0.0652', '0.1223', '-0.1871', '0.01445', '0.06125']",,0009164,,,,,
mondo:0030921,"intellectual disability, autosomal dominant 55, with seizures","['mental retardation, autosomal dominant 55, with seizures', 'MRD55', 'intellectual disability, autosomal dominant 55, with seizures', 'autosomal dominant mental retardation 55', 'autosomal dominant intellectual disability 55']",0080227,617831,442835,CN757796,,,,,,,,
mondo:0030922,"intellectual disability, autosomal dominant 56","['intellectual disability, autosomal dominant 56', 'mental retardation, autosomal dominant 56', 'MRD56', 'autosomal dominant intellectual disability 56', 'autosomal dominant mental retardation 56']",0080226,617854,442835,CN787270,"['-0.03012', '0.04907', '0.01762', '-0.0338', '0.01877', '-0.09735', '-0.00158', '0.09705', '-0.05173', '-0.05072', '-0.02855', '0.00645', '0.01496', '-0.007385', '0.006817', '-0.02408', '-0.01625', '-0.03638', '-0.0205', '-0.1462', '-0.004498', '-0.003891', '0.0419', '-0.02698', '0.05045', '-0.005566', '-0.01945', '-0.02376', '0.003763', '-0.04703', '0.07153', '-0.01602', '0.07544', '0.0437', '-0.004272', '-0.03592', '-0.01086', '-0.04523', '-0.002464', '-0.07495', '0.06012', '-0.0814', '0.00999', '-0.00951', '-0.02034', '-0.0905', '-0.02339', '0.03204', '0.007153', '0.0176', '-0.01869', '-0.005543', '-0.03026', '-0.02429', '-0.014984', '-0.04782', '0.08795', '-0.01578', '-0.08514', '0.0302', '0.0409', '0.02637', '0.01419', '0.004078', '0.00534', '0.0126', '0.0639', '0.05737', '-0.06177', '0.05106', '-0.05817', '-0.008316', '0.01535', '-0.04352', '0.05048', '0.0517', '0.0221', '4.91e-05', '-0.0465', '-0.02081', '0.004578', '0.011925', '-0.009964', '0.08936', '0.0016165', '0.0408', '0.01622', '0.07886', '0.0811', '0.05133', '0.0319', '0.0696', '-0.004562', '0.01016', '0.1592', '0.04102', '0.0829', '-0.08215', '0.00799', '0.02911']",,,,,,,
mondo:0030923,frontotemporal dementia and/or amyotrophic lateral sclerosis,,,,,,,,,,,,,
mondo:0030924,proteasome-associated autoinflammatory syndrome 5,"['PRAAS5', 'proteasome-associated autoinflammatory syndrome 5']",,619175,,,,,,,,,,
mondo:0030925,oocyte maturation defect 10,"['oocyte maturation defect 10', 'OOMD10']",,619176,,,,,,,,,,
mondo:0030926,spermatogenic failure 51,"['spermatogenic failure 51', 'SPGF51']",0112273,619177,,,,,,,,,,
mondo:0030927,myofibrillar myopathy 11,"['myopathy, congenital, with eccentric cores', 'MFM11', 'myofibrillar myopathy 11']",0081338,619178,,,,,,,,,,
mondo:0030928,"microcephaly 26, primary, autosomal dominant","['MCPH26', 'microcephaly 26, primary, autosomal dominant']",,619179,,,,,,,,,,
mondo:0030929,"microcephaly 27, primary, autosomal dominant","['MCPH27', 'microcephaly 27, primary, autosomal dominant']",,619180,,,,,,,,,,
mondo:0030930,neurodevelopmental disorder with or without early-onset generalized epilepsy,['NEDEGE'],,619157,,,,,,,,,,
mondo:0030931,proteasome-associated autoinflammatory syndrome 4,"['PRAAS4', 'proteasome-associated autoinflammatory syndrome 4']",,619183,,,,,,,,,,
mondo:0030933,Joubert syndrome 37,"['Joubert syndrome 37', 'JBTS37']",,619185,,,,,,,,,,
mondo:0030934,"intellectual developmental disorder, autosomal dominant 64","['intellectual developmental disorder, autosomal dominant 64', 'MRD64', 'mental retardation, autosomal dominant 64']",,619188,,,,,,,,,,
mondo:0030935,"mitochondrial complex 2 deficiency, nuclear type 2","['mitochondrial complex II deficiency, nuclear type 2', 'mitochondrial complex 2 deficiency, nuclear type 2', 'MC2DN2']",,619166,,,,,,,,,,
mondo:0030936,"epilepsy, progressive myoclonic, 12","['epilepsy, progressive myoclonic, 12', 'EPM12']",,619191,,,,,,,,,,
mondo:0030937,"mitochondrial complex 2 deficiency, nuclear type 3","['mitochondrial complex 2 deficiency, nuclear type 3', 'MC2DN3', 'mitochondrial complex II deficiency, nuclear type 3']",,619167,,,,,,,,,,
mondo:0030938,spermatogenic failure 52,"['SPGF52', 'spermatogenic failure 52']",0112270,619202,,,,,,,,,,
mondo:0030939,premature ovarian failure 18,"['premature ovarian failure 18', 'POF18']",0112269,619203,,,,,,,,,,
mondo:0030941,erythrokeratodermia variabilis et progressiva 7,"['erythrokeratodermia variabilis et progressiva 7', 'EKVP7']",,619209,,,,,,,,,,
mondo:0030947,"neurodegeneration, childhood-onset, with hypotonia, respiratory insufficiency, and brain imaging abnormalities","['CONRIBA', 'neurodegeneration, childhood-onset, hypotonia, respiratory insufficiency and brain imaging abnormalities']",,619173,610573,,,,,,,,,
mondo:0030953,"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2","['short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies 2', 'SSFSC2', 'short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies']",0112358,619184,,,,,,,,,,
mondo:0030957,developmental and epileptic encephalopathy 103,"['DEE103', 'developmental and epileptic encephalopathy 103']",0070389,619913,,,,,,,,,,
mondo:0030958,"dystonia 35, childhood-onset","['DYT35', 'dystonia 35, childhood-onset']",,619921,,,,,,,,,,
mondo:0030961,Olmsted syndrome 2,"['OLMS2', 'palmoplantar keratoderma, mutilating, with periorificial keratotic plaques 2', 'Olmsted syndrome 2']",,619208,,,,,,,,,,
mondo:0030962,"nephrotic syndrome, type 23","['NPHS23', 'nephrotic syndrome, type 23']",0112266,619201,,,,,,,,,,
mondo:0030963,Li-Campeau syndrome,['LICAS'],,619189,,,,,,,,,,
mondo:0030964,"intellectual developmental disorder, autosomal dominant 67","['MRD67', 'mental retardation, autosomal dominant 67', 'intellectual developmental disorder, autosomal dominant 67']",,619927,,,,,,,,,,
mondo:0030966,neurofacioskeletal syndrome with or without renal agenesis,"['NFSRA', 'Neurodevelopmental Disorder With Corpus Callosum Agenesis, Craniofacial Dysmorphism, and Skeletal Anomalies, With or Without Renal Agenesis']",,619194,,,,,,,,,,
mondo:0030967,"deafness, congenital, and adult-onset progressive leukoencephalopathy",['DEAPLE'],,619196,,,,,,,,,,
mondo:0030968,"intellectual developmental disorder, autosomal recessive 76","['MRT76', 'mental retardation, autosomal recessive 76', 'intellectual developmental disorder, autosomal recessive 76']",0081235,619931,,,,,,,,,,
mondo:0030969,"intellectual developmental disorder, autosomal dominant 68","['mental retardation, autosomal dominant 68', 'MRD68', 'intellectual developmental disorder, autosomal dominant 68']",,619934,,,,,,,,,,
mondo:0030970,"immunodeficiency 106, susceptibility to viral infections","['immunodeficiency 106, susceptibility to viral infections', 'IMD106', 'IFNAR1 deficiency']",,619935,,,,,,,,,,
mondo:0030971,immunodeficiency 78 with autoimmunity and developmental delay,"['TPP2 deficiency', 'IMD78', 'immunodeficiency 78 with autoimmunity and developmental delay']",,619220,,,,,,,,,,
mondo:0030972,spermatogenic failure 74,"['SPGF74', 'spermatogenic failure 74']",,619937,,,,,,,,,,
mondo:0030973,immunodeficiency 77,"['IMD77', 'immunodeficiency 77']",,619223,,,,,,,,,,
mondo:0030974,"mitochondrial complex 2 deficiency, nuclear type 4","['MC2DN4', 'mitochondrial complex 2 deficiency, nuclear type 4', 'mitochondrial complex II deficiency, nuclear type 4']",,619224,,,,,,,,,,
mondo:0030975,premature ovarian failure 20,"['premature ovarian failure 20', 'POF20']",,619938,,,,,,,,,,
mondo:0030976,oculomotor-abducens synkinesis,['OCABSN'],,619215,,,,,,,,,,
mondo:0030977,"neuropathy, hereditary motor, with myopathic features",['HMNMYO'],,619216,,,,,,,,,,
mondo:0030978,"endove syndrome, limb-only type","['ENDOVESL', 'Mesomelia of Lower Extremities With Hand and Foot Anomalies']",,619217,,,,,,,,,,
mondo:0030979,"endove syndrome, limb-brain type","['ENDOVESLB', 'Mesomelia of Lower Extremities With Hand, Foot, and Brain Anomalies']",,619218,,,,,,,,,,
mondo:0030981,immunodeficiency 79,"['immunodeficiency 79', 'IMD79', 'CD4 Deficiency']",0112277,619238,,,,,,,,,,
mondo:0030982,sulfide quinone oxidoreductase deficiency,"['SQORD', 'sulfide:quinone oxidoreductase deficiency']",,619221,,,,,,,,,,
mondo:0030983,"Waardenburg syndrome, IIa 2F","['Waardenburg syndrome, IIa 2F', 'WS2F']",,619947,,,,,,,,,,
mondo:0030984,spermatogenic failure 75,"['spermatogenic failure 75', 'SPGF75']",,619949,,,,,,,,,,
mondo:0030985,premature ovarian failure 19,"['POF19', 'premature ovarian failure 19']",0112278,619245,,,,,,,,,,
mondo:0030986,"blistering, acantholytic, of oral and laryngeal mucosa",['ABOLM'],,619226,,,,,,,,,,
mondo:0030987,"vertebral, cardiac, tracheoesophageal, renal, and limb defects","['VCTERL syndrome', 'VCTERL']",,619227,,,,,,,,,,
mondo:0030988,developmental delay with dysmorphic facies and dental anomalies,['DEFDA'],,619228,,,,,,,,,,
mondo:0030989,spermatogenic failure 53,"['SPGF53', 'spermatogenic failure 53']",0112279,619258,,,,,,,,,,
mondo:0030990,Kohlschutter-Tonz syndrome-like,['KTZSL'],,619229,,,,,,,,,,
mondo:0030991,bile acid conjugation defect 1,['BACD1'],,619232,,,,,,,,,,
mondo:0030992,"short stature, oligodontia, dysmorphic facies, and motor delay",['SOFM'],,619234,,,,,,,,,,
mondo:0030993,Tessadori-Van Haaften neurodevelopmental syndrome 3,"['Tessadori-Van Haaften neurodevelopmental syndrome 3', 'TEVANED3']",,619950,,,,,,,,,,
mondo:0030994,neurodevelopmental disorder with or without autism or seizures,['NEDAUS'],,619239,,,,,,,,,,
mondo:0030995,global developmental delay with speech and behavioral abnormalities,['GDSBA'],,619243,,,,,,,,,,
mondo:0030996,"bleeding disorder, platelet-type, 24","['Glanzmann Thrombasthenia-Like With Macrothrombocytopenia 2', 'bleeding disorder, platelet-type, 24', 'BDPLT24', 'bleeding disorder, platelet-type, 24, autosomal dominant']",,619271,,,,,,,,,,
mondo:0030997,"mitochondrial complex 1 deficiency, nuclear type 37","['MC1DN37', 'mitochondrial complex 1 deficiency, nuclear type 37', 'mitochondrial complex I deficiency, nuclear type 37']",,619272,,,,,,,,,,
mondo:0030998,"hearing loss, autosomal dominant 80","['DFNA80', 'deafness, autosomal dominant 80']",,619274,,,,,,,,,,
mondo:0030999,neurodevelopmental disorder with cerebral atrophy and variable facial dysmorphism,['NEDCAFD'],,619244,,,,,,,,,,
mondo:0031000,Tessadori-Van Haaften neurodevelopmental syndrome 4,"['Tessadori-Van Haaften neurodevelopmental syndrome 4', 'TEVANED4']",,619951,,,,,,,,,,
mondo:0031001,vitreoretinopathy with phalangeal epiphyseal dysplasia,['VPED'],,619248,,,,,,,,,,
mondo:0031002,Baralle-Macken syndrome,"['neurodevelopmental disorder with cataracts and variable microcephaly', 'BARMACS']",,619255,,,,,,,,,,
mondo:0031003,"hypercholanemia, familial, 2","['hypercholanemia, familial 2', 'FHCA2', 'NTCP Deficiency']",,619256,,,,,,,,,,
mondo:0031006,neurodegeneration with ataxia and late-onset optic atrophy,['NDAXOA'],,619259,,,,,,,,,,
mondo:0031007,"spondyloepiphyseal dysplasia, sensorineural hearing loss, impaired intellectual development, and leber congenital amaurosis","['SHILCA syndrome', 'SHILCA', 'spondyloepiphyseal dysplasia, sensorineural hearing loss, intellectual developmental disorder, and Leber congenital amaurosis']",0112290,619260,611207,,,,,,,,,
mondo:0031008,"nephrotic syndrome, type 24","['NPHS24', 'idiopathic steroid-resistant nephrotic syndrome', 'idiopathic SRNS']",,619263,567548,,,,,,,,,
mondo:0031009,Glanzmann thrombasthenia 2,"['bleeding disorder, platelet-type, 23', 'GT2']",,619267,,,,,,,,,,
mondo:0031010,odontochondrodysplasia 2 with hearing loss and diabetes,"['ODCD2', 'ondontochondrodysplasia 2 with hearing loss and diabetes']",,619269,,,,,,,,,,
mondo:0031011,neurodevelopmental disorder with dysmorphic facies and variable seizures,['NEDDFAS'],,619264,,,,,,,,,,
mondo:0031012,autoimmune uveitis,,0040088,,,,,,,,,,,
mondo:0031013,autoimmune optic neuritis,,0040089,,,,,,,,,,,
mondo:0031014,autoimmune gastritis,,0040090,,,,,C95752,,,,,,
mondo:0031019,"spastic paraplegia 87, autosomal recessive","['SPG87', 'spastic paraplegia 87, autosomal recessive']",,619966,,,,,,,,,,
mondo:0031021,developmental and epileptic encephalopathy 104,"['DEE104', 'developmental and epileptic encephalopathy 104']",0070390,619970,,,,,,,,,,
mondo:0031028,developmental and epileptic encephalopathy 105 with hypopituitarism,"['DEE105', 'developmental and epileptic encephalopathy 105 with hypopituitarism']",0070391,619983,,,,,,,,,,
mondo:0031030,"immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection","['immunodeficiency 107, susceptibility to invasive staphylococcus aureus infection', 'IMD107']",,619986,,,,,,,,,,
mondo:0031031,"intellectual developmental disorder, autosomal recessive 77","['MRT77', 'intellectual developmental disorder, autosomal recessive 77']",0081236,619988,,,,,,,,,,
mondo:0031037,famililal cerebral cavernous malformations,"['hereditary cerebral cavernoma', 'hereditary brain cavernous hemangioma', 'hereditary cerebral cavernous malformation', 'cavernous angiomatous malformations', 'familial brain cavernous angioma', 'cerebral cavernous malformations', 'familial cerebral cavernoma', 'cerebral capillary malformations', 'familial brain cavernous hemangioma', 'cavernous malformations of CNS and retina', 'hyperkeratotic cutaneous capillary-Venous malformations associated with cerebral capillary malformations', 'hereditary brain cavernous angioma', 'cavernous angioma, familial', 'familial cerebral cavernous malformation', 'CCM']",,,221061,C2931263,"['0.3523', '0.1957', '-0.1517', '0.1532', '0.1732', '0.2844', '0.2146', '0.958', '-0.5312', '0.1687', '-0.228', '-0.5103', '-0.12225', '-0.277', '0.11017', '-0.126', '-0.418', '-0.4683', '-0.2974', '-0.736', '0.06216', '0.3354', '0.304', '-0.219', '-0.2659', '0.1965', '-0.4536', '0.1865', '0.4377', '0.4202', '0.3435', '-0.4958', '0.537', '0.776', '-0.301', '0.3184', '0.1561', '0.286', '0.4426', '0.1915', '0.6475', '-0.4866', '0.6084', '-0.4841', '-0.0639', '0.2532', '-0.3462', '0.1084', '0.002794', '0.02542', '0.224', '0.9155', '0.1858', '0.1416', '-0.004536', '0.3337', '0.8467', '0.06573', '-1.007', '0.2207', '-0.0957', '-0.01878', '0.1558', '-0.553', '-0.6396', '0.4778', '0.518', '0.4602', '-0.1826', '0.336', '-0.3154', '0.2101', '-0.1959', '-0.2844', '0.672', '0.5303', '0.6724', '-0.341', '-0.10504', '-0.1686', '-0.617', '-0.2133', '0.2471', '0.10156', '0.5664', '-0.1865', '0.3406', '0.745', '-0.5693', '-0.3066', '0.6274', '0.3289', '-0.1743', '0.03128', '0.2776', '-0.0999', '0.539', '0.1981', '0.0976', '0.1157']",,,,,,,
mondo:0031040,"cholestasis, progressive familial intrahepatic, 12","['PFIC12', 'cholestasis, isolated low-ggt', 'cholestasis, progressive familial intrahepatic, 12']",,620010,,,,,,,,,,
mondo:0031043,lymphatic malformation 12,"['lymphatic malformation 12', 'central conducting lymphatic anomaly', 'LMPHM12']",0081030,620014,,,,,,,,,,
mondo:0031044,"advance sleep phase syndrome, familial, 4","['FASPS4', 'advance sleep phase syndrome, familial, 4']",,620015,,,,,,,,,,
mondo:0031045,"arthrogryposis, distal, IIa 11","['arthrogryposis, distal, IIa 11', 'DA11']",,620019,,,,,,,,,,
mondo:0031047,"stickler syndrome, IIa 6","['STL6', 'stickler syndrome, IIa 6']",,620022,,,,,,,,,,
mondo:0031052,developmental and epileptic encephalopathy 106,"['developmental and epileptic encephalopathy 106', 'DEE106']",0070392,620028,,,,,,,,,,
mondo:0031054,"ciliary dyskinesia, primary, 48, without situs inversus","['CILD48', 'ciliary dyskinesia, primary, 48, without situs inversus']",,620032,,,,,,,,,,
mondo:0031055,developmental and epileptic encephalopathy 107,"['developmental and epileptic encephalopathy 107', 'DEE107']",0070393,620033,,,,,,,,,,
mondo:0031057,"dyskeratosis congenita, digenic","['DKCD', 'dyskeratosis congenita, digenic']",,620040,,,,,,,,,,
mondo:0031060,"microcephaly 29, primary, autosomal recessive","['MCPH29', 'microcephaly 29, primary, autosomal recessive']",,620047,,,,,,,,,,
mondo:0031061,"nephrotic syndrome, IIa 26","['nephrotic syndrome, IIa 26', 'NPHS26']",,620049,,,,,,,,,,
mondo:0031062,polycystic kidney disease 7,"['polycystic kidney disease 7', 'PKD7']",,620056,,,,,,,,,,
mondo:0031068,"Charcot-Marie-Tooth disease, axonal, IIa 2II","['charcot-marie-tooth neuropathy, IIa 2II', 'charcot-marie-tooth disease, axonal, IIa 2II', 'CMT2II']",,620068,,,,,,,,,,
mondo:0031071,Diamond-Blackfan anemia 21,"['diamond-blackfan anaemia 21', 'DBA21', 'diamond-blackfan anemia 21']",,620072,,,,,,,,,,
mondo:0031077,spermatogenic failure 76,"['SPGF76', 'spermatogenic failure 76']",,620084,,,,,,,,,,
mondo:0031083,spermatogenic failure 77,"['spermatogenic failure 77', 'SPGF77']",,620103,,,,,,,,,,
mondo:0031084,"amelogenesis imperfecta, IIa 1K","['amelogenesis imperfecta, IIa 1K', 'amelogenesis imperfecta, hypoplastic IIa 1K', 'AI1K']",,620104,,,,,,,,,,
mondo:0031115,dyskinesia with orofacial involvement,,,,,,,,,,,,,
mondo:0031166,"macular dystrophy, retinal",,,,,,,,,,,,,
mondo:0031169,odontochondrodysplasia,,,,,,,,,,,,,
mondo:0031199,inherited interstitial lung disease,,,,,,,,,,,,,
mondo:0031200,Bryant-Li-Bhoj neurodevelopmental syndrome,,,,,,,,,,,,,
mondo:0031213,restrictive dermopathy,,0060762,,,,,,,,,,,
mondo:0031219,mismatch repair cancer syndrome,,0112182,,,,,,,,,,,
mondo:0031230,"mitochondrial complex II deficiency, nuclear type",,,,,,,,,,,,,
mondo:0031240,familial panic disorder,,,,,,,,,,,,,
mondo:0031257,high altitude pulmonary edema,,,,330012,,,,,,,,,
mondo:0031280,Stuve-Wiedemann syndrome,,,,,,,,,,,,,
mondo:0031322,triopia,,,,3374,,,,,,,Q15.8,,
mondo:0031323,cardiac valvular defect,,,,,,,,,,,,,
mondo:0031329,"craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome",,0081072,,,,,,,,,,,
mondo:0031332,Glanzmann thrombasthenia 1,"['platelet-type bleeding disorder 2', 'deficiency of glycoprotein complex IIb-IIIa', 'GP IIb-IIIa Complex, deficiency of', 'Thrombocytasthenia', 'Glanzmann^s thrombasthenia', 'Diacyclothrombopathia 2B 3A', 'bleeding disorder, Platelet-type, 2', 'deficiency of platelet fibrinogen receptor', 'Glanzmann thrombasthenia type A', 'Platelet glycoprotein 2B 3A deficiency', 'platelet glycoprotein IIb-IIIa deficiency', 'BDPLT2', 'GT', 'Platelet fibrinogen receptor, deficiency of', 'deficiency of GP IIb-IIIa complex', 'glycoprotein IIb/IIIa defect', 'Platelet glycoprotein IIb-IIIa deficiency', 'thrombasthenia', 'Glanzmann thrombasthenia', 'glycoprotein Complex IIb-IIIa, deficiency of', 'deficiency of GP 2B 3A complex', 'thrombasthenia of Glanzmann and Naegeli']",2219,273800,,,,C61249,,D013915,,,,
mondo:0031376,congenital disorder of deglycosylation,,,,,,,,,,,,,
mondo:0031384,"autoinflammatory syndrome, familial, Behcet-like",,,,,,,,,,,,,
mondo:0031386,cardioacrofacial dysplasia,,,,,,,,,,,,,
mondo:0031400,Tessadori-Van-Haaften neurodevelopmental syndrome,,,,,,,,,,,,,
mondo:0031415,Carey-Fineman-Ziter syndrome,,,,1358,,"['-0.241', '-0.0483', '-0.04755', '-0.1224', '0.2332', '-0.4954', '0.2217', '0.602', '-0.4424', '-0.02771', '-0.1377', '-0.384', '-0.02783', '-0.2734', '-0.2717', '0.00486', '-0.001879', '-0.354', '-0.4236', '-0.5747', '0.2678', '0.06384', '0.128', '-0.528', '0.10803', '-0.0586', '0.2812', '0.1854', '-0.09656', '-0.1705', '0.01746', '-0.0285', '0.4355', '0.3298', '-0.1109', '0.1744', '-0.02924', '-0.384', '-0.1515', '0.1271', '-0.1315', '-0.3838', '-0.4146', '0.01441', '-0.142', '0.572', '-0.1694', '0.3987', '-0.673', '0.3594', '0.1912', '0.452', '-0.1869', '0.1197', '-0.256', '-0.4294', '0.1017', '-0.1165', '-0.1248', '0.3499', '0.4253', '0.2477', '-0.1836', '0.1231', '-0.8193', '-0.4082', '0.1675', '0.2957', '-0.8364', '0.3767', '-0.1782', '0.5044', '-0.2292', '-0.01458', '0.01743', '-0.0461', '0.3748', '-0.02995', '-0.2368', '0.087', '-0.1227', '0.2494', '0.481', '1.019', '-0.03598', '-0.05264', '-0.1598', '0.2537', '0.10693', '-0.341', '0.1127', '0.412', '0.2343', '0.1902', '0.9053', '-0.265', '0.2957', '-0.0234', '0.0977', '0.03047']",,,,,,,
mondo:0031421,Olmsted syndrome,"['palmoplantar and periorificial keratoderma', 'palmoplantar keratoderma, mutilating, with periorificial keratotic plaques', 'mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques']",0112011,,659,C2609071,"['-0.01785', '0.313', '-0.05905', '-0.11053', '0.08795', '-0.4675', '-0.339', '-0.22', '0.00418', '0.1418', '-0.067', '0.1616', '-0.1643', '-0.139', '-0.2834', '0.03632', '0.2632', '-0.426', '0.191', '-0.804', '-0.0923', '-0.164', '0.3481', '-0.02132', '0.1724', '0.3345', '-0.1625', '0.03564', '0.0766', '-0.2378', '0.1735', '-0.02632', '0.0957', '0.1765', '0.3032', '-0.1091', '0.04614', '-0.084', '-0.02028', '-0.314', '0.0673', '-0.572', '0.10297', '-0.1075', '0.03033', '-0.314', '-0.2595', '0.3577', '0.05963', '-0.07336', '-0.1425', '-0.177', '0.231', '0.1101', '-0.4607', '-0.03683', '0.537', '-0.1788', '-0.514', '-0.02469', '0.0499', '0.02231', '-0.194', '-0.1294', '0.1891', '-0.04837', '0.4692', '0.3591', '0.1558', '0.6543', '-0.4175', '-0.2197', '0.2656', '-0.01764', '0.01898', '-0.02051', '-0.05923', '-0.08356', '-0.07336', '-0.2957', '0.04333', '0.1016', '0.0886', '0.1249', '0.1449', '-0.2424', '-0.065', '0.4387', '0.3423', '0.2686', '0.3547', '0.2942', '0.274', '0.19', '0.361', '-0.03937', '0.3806', '-0.507', '0.0611', '0.0096']",,,,,,10068842,
mondo:0031422,familial mucolipidosis,,,,,,,,,,,,,
mondo:0031432,"thyroid hormone metabolism, abnormal",,,,,,,,,,,,,
mondo:0031439,"short stature, facial dysmorphism, and skeletal anomalies with or without cardiac anomalies",,,,,,,,,,,,,
mondo:0031446,"hypercholanemia, familial 1","['hereditary hypercholanemia', 'FHCA1']",,607748,238475,C1843139,"['-0.5933', '0.00759', '-0.012985', '0.1628', '0.551', '-0.178', '-0.9004', '0.674', '-0.2673', '0.2983', '0.084', '0.2336', '0.3071', '-0.1746', '0.011154', '-0.05624', '0.1735', '0.1482', '-0.2158', '-0.607', '-0.292', '-0.4343', '0.271', '-0.27', '0.07184', '0.0602', '-0.0843', '-0.04318', '-0.05972', '-0.815', '0.762', '0.0761', '0.10364', '0.06805', '-0.4094', '-0.0939', '-0.6055', '-0.3596', '0.09174', '-0.661', '0.2402', '-0.5815', '0.1853', '-0.1826', '-0.654', '-0.3123', '0.1296', '-0.0472', '0.0951', '-0.4683', '-0.4158', '-0.1934', '-0.1843', '0.04752', '-0.3486', '0.099', '0.539', '-0.2341', '-0.1162', '-0.1598', '0.6875', '0.2374', '0.447', '-0.5576', '0.1614', '0.238', '0.5815', '0.1354', '-0.7827', '0.01584', '-0.0874', '0.10785', '-0.0855', '0.3606', '0.09576', '0.1461', '0.08417', '-0.0483', '0.04706', '0.01872', '0.4016', '-0.1061', '-0.1007', '-0.08344', '-0.0382', '-0.1921', '0.1235', '0.1995', '0.4639', '0.3035', '0.2522', '0.2308', '-0.1906', '-0.00905', '0.8203', '-0.0972', '0.2057', '-0.2861', '-0.246', '-0.2275']",,,C564336,,,,
mondo:0031447,"macrothrombocytopenia, isolated",,,,,,,,,,,,,
mondo:0031481,"microcephaly, epilepsy, and diabetes syndrome 1","['primary microcephaly-epilepsy-permanent neonatal diabetes syndrome', 'microcephaly, epilepsy, and diabetes syndrome', 'MEDS1']",,614231,306558,C3280240,"['0.06915', '0.2383', '0.329', '-0.4246', '-0.2125', '-0.1766', '0.3044', '0.3657', '-0.6606', '0.0812', '-0.4182', '-0.5913', '-0.04266', '-0.352', '-0.2537', '-0.048', '0.2334', '-0.112', '-0.2573', '-0.4893', '0.2109', '-0.0836', '0.05545', '0.10596', '0.04858', '-0.1232', '0.004246', '-0.1521', '0.2191', '-0.347', '0.1915', '0.075', '0.5283', '0.1702', '0.2139', '0.4495', '-0.1458', '-0.1173', '-0.3708', '-0.4229', '-0.12103', '-0.2644', '-0.0169', '0.2131', '-0.3083', '-0.1511', '0.0686', '0.505', '-0.2812', '0.1174', '-0.2732', '0.3904', '-0.282', '-0.05618', '-0.2856', '-0.10944', '-0.2155', '-0.3193', '-0.08954', '0.1982', '-0.04205', '0.1554', '-0.0976', '-0.2031', '-0.401', '0.006596', '0.4104', '0.3215', '-0.2467', '0.4744', '-0.23', '0.367', '0.316', '0.1022', '-0.3372', '-0.1906', '0.579', '-0.2043', '-0.283', '0.1486', '-0.0235', '0.3237', '-0.1678', '0.3672', '-0.02216', '0.1149', '-0.0825', '0.5073', '0.4988', '0.1427', '0.1971', '0.2705', '0.3396', '0.2634', '0.4602', '0.1929', '0.3945', '-0.2676', '0.3345', '0.3394']",,,,,,,
mondo:0031520,familial severe combined immunodeficiency,,,,,,,,,,,,,
mondo:0031615,familial bent bone dysplasia syndrome,,,,,,,,,,,,,
mondo:0031632,"developmental delay with short stature, dysmorphic facial features, and sparse hair",,,,,,,,,,,,,
mondo:0031646,Braddock-Carey syndrome,,,,,,,,,,,,,
mondo:0032485,intellectual developmental disorder 61,"['INTELLECTUAL DEVELOPMENTAL DISORDER 61', 'MRD61', 'Mental Retardation, Autosomal Dominant 61']",,618009,,,,,,,,,,
mondo:0032526,spinocerebellar ataxia 48,"['SCA48', 'SPINOCEREBELLAR ATAXIA 48']",0111746,618093,631103,,,,,,,,,
mondo:0032564,hennekam lymphangiectasia-lymphedema syndrome 3,"['HENNEKAM LYMPHANGIECTASIA-LYMPHEDEMA SYNDROME 3', 'HKLLS3']",,618154,,,,,,,,,,
mondo:0032565,"ophthalmoplegia, external, with rib and vertebral anomalies","['EORVA', 'OPHTHALMOPLEGIA, EXTERNAL, WITH RIB AND VERTEBRAL ANOMALIES']",,618155,,,,,,,,,,
mondo:0032566,squalene synthase deficiency,"['neurodevelopmental disorder with low cholesterol and abnormal urine organic acids', 'SQSD', 'SQUALENE SYNTHASE DEFICIENCY']",,618156,,,,,,,,,,
mondo:0032567,"isolated growth hormone deficiency, type 4","['IGHD4', 'Dwarfism of Sindh', 'Isolated Growth Hormone Deficiency, Type Ib', 'Isolated Growth Hormone Deficiency, Type Ib, Formerly', 'growth hormone deficiency, isolated, type IV', 'ISOLATED GROWTH HORMONE DEFICIENCY, TYPE IV']",,618157,,,,,,,,,,
mondo:0032568,"intellectual developmental disorder with macrocephaly, seizures, and speech delay","['INTELLECTUAL DEVELOPMENTAL DISORDER WITH MACROCEPHALY, SEIZURES, AND SPEECH DELAY', 'IDDMSSD']",,618158,,,,,,,,,,
mondo:0032569,"isolated growth hormone deficiency, type 5","['pituitary hormone deficiency, combined or isolated, 7', 'ISOLATED GROWTH HORMONE DEFICIENCY, TYPE V', 'IGHD5']",,618160,,,,,,,,,,
mondo:0032570,Joubert syndrome 35,"['JOUBERT SYNDROME 35', 'JBTS35']",,618161,,,,,,,,,,
mondo:0032571,"spondyloepimetaphyseal dysplasia, Krakow type","['SEMDK', 'SPONDYLOEPIMETAPHYSEAL DYSPLASIA, KRAKOW TYPE', 'Immunoosseous Dysplasia, Krakow Type']",,618162,,,,,,,,,,
mondo:0032572,"cardiac, facial, and digital anomalies with developmental delay","['CAFDADD', 'CARDIAC, FACIAL, AND DIGITAL ANOMALIES WITH DEVELOPMENTAL DELAY']",,618164,,,,C179868,,,,,,
mondo:0032573,bone marrow failure syndrome 5,"['BONE MARROW FAILURE SYNDROME 5', 'BMFS5']",,618165,,,,,,,,,,
mondo:0032574,"osteochondrodysplasia, brachydactyly, and overlapping malformed digits","['OSTEOCHONDRODYSPLASIA, BRACHYDACTYLY, AND OVERLAPPING MALFORMED DIGITS', 'OCBMD']",,618167,,,,,,,,,,
mondo:0032575,diarrhea 9,"['DIAR9', 'DIARRHEA 9']",,618168,,,,,,,,,,
mondo:0032577,retinitis pigmentosa 83,"['RP83', 'RETINITIS PIGMENTOSA 83']",0112140,618173,,,,,,,,,,
mondo:0032578,"cortical dysplasia, complex, with other brain malformations 9","['CDCBM9', 'CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 9']",,618174,,,,,,,,,,
mondo:0032579,warburg-cinotti syndrome,"['WARBURG-CINOTTI SYNDROME', 'WRCN']",,618175,,,,,,,,,,
mondo:0032580,"nephrotic syndrome, type 17","['NEPHROTIC SYNDROME, TYPE 17', 'NPHS17']",0080392,618176,,,,,,,,,,
mondo:0032581,"nephrotic syndrome, type 18","['NPHS18', 'NEPHROTIC SYNDROME, TYPE 18']",0080393,618177,,,,,,,,,,
mondo:0032582,"nephrotic syndrome, type 19","['NEPHROTIC SYNDROME, TYPE 19', 'NPHS19']",0080394,618178,,,,,,,,,,
mondo:0032583,"microcephaly 24, primary, autosomal recessive","['MICROCEPHALY 24, PRIMARY, AUTOSOMAL RECESSIVE', 'MCPH24']",,618179,,,,,,,,,,
mondo:0032584,"ectodermal dysplasia 14, hair/tooth type with or without hypohidrosis","['ECTODERMAL DYSPLASIA 14, HAIR/TOOTH TYPE WITH OR WITHOUT HYPOHIDROSIS', 'ECTD14']",0111662,618180,,,,,,,,,,
mondo:0032586,"diarrhea 10, protein-losing enteropathy type","['DIAR10', 'DIARRHEA 10, PROTEIN-LOSING ENTEROPATHY TYPE']",,618183,,,,,,,,,,
mondo:0032588,periventricular nodular heterotopia 8,"['PERIVENTRICULAR NODULAR HETEROTOPIA 8', 'PVNH8']",,618185,,,,,,,,,,
mondo:0032590,ovarian dysgenesis 8,"['OVARIAN DYSGENESIS 8', 'ODG8']",0080500,618187,,,,,,,,,,
mondo:0032591,"hyperparathyroidism, transient neonatal","['hyperparathyroidism, transient neonatal', 'HRPTTN']",,618188,,,,,,,,,,
mondo:0032592,"cardiomyopathy, dilated, 2c","['CMD2C', 'CARDIOMYOPATHY, DILATED, 2C']",0081159,618189,,,,,,,,,,
mondo:0032594,intellectual developmental disorder and retinitis pigmentosa; IDDRP,"['IDDRP', 'INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA']",,618195,,,,,,,,,,
mondo:0032596,"myasthenic syndrome, congenital, 23, presynaptic","['MYASTHENIC SYNDROME, CONGENITAL, 23, PRESYNAPTIC', 'CMS23']",,618197,,,,,,,,,,
mondo:0032597,"myasthenic syndrome, congenital, 24, presynaptic","['MYASTHENIC SYNDROME, CONGENITAL, 24, PRESYNAPTIC', 'CMS24']",,618198,,,,,,,,,,
mondo:0032598,"developmental and epileptic encephalopathy, 68","['EIEE68', 'epileptic encephalopathy, early infantile, 68', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 68', 'developmental and epileptic encephalopathy 68', 'DEE68']",0112204,618201,,,,,,,,,,
mondo:0032599,immunodeficiency 15a,"['IMMUNODEFICIENCY 15A', 'IMD15A']",0111960,618204,,,,,,,,,,
mondo:0032600,Snijders Blok-Campeau syndrome,"['SNIBCPS', 'intellectual developmental disorder with macrocephaly, speech delay, and dysmorphic facies', 'SNIJDERS BLOK-CAMPEAU SYNDROME']",,618205,599082,,,,,,,,,
mondo:0032601,"inflammatory bowel disease, immunodeficiency, and encephalopathy","['IBDIMDE', 'INFLAMMATORY BOWEL DISEASE, IMMUNODEFICIENCY, AND ENCEPHALOPATHY']",,618213,565788,,,,,,,,,
mondo:0032603,"polydactyly, postaxial, type A9","['PAPA9', 'POLYDACTYLY, POSTAXIAL, TYPE A9']",,618219,,,,,,,,,,
mondo:0032604,retinitis pigmentosa 84,"['RP84', 'RETINITIS PIGMENTOSA 84']",0112141,618220,,,,,,,,,,
mondo:0032605,"intellectual disability, autosomal recessive 66","['MRT66', 'MENTAL RETARDATION, AUTOSOMAL RECESSIVE 66', 'intellectual developmental disorder, autosomal recessive 66']",0081227,618221,,,,,,,,,,
mondo:0032606,"mitochondrial complex 1 deficiency, nuclear type 2","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 2', 'MC1DN2']",0112083,618222,,,,,,,,,,
mondo:0032607,vertebral anomalies and variable endocrine and T-cell dysfunction,"['VERTEBRAL ANOMALIES AND VARIABLE ENDOCRINE AND T-CELL DYSFUNCTION', 'VETD']",0070345,618223,,,,,,,,,,
mondo:0032608,"mitochondrial complex 1 deficiency, nuclear type 3","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 3', 'MC1DN3']",0112093,618224,,,,,,,,,,
mondo:0032609,"mitochondrial complex 1 deficiency, nuclear type 4","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 4', 'MC1DN4']",0112082,618225,,,,,,,,,,
mondo:0032610,"mitochondrial complex 1 deficiency, nuclear type 5","['MC1DN5', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 5']",0112068,618226,,,,,,,,,,
mondo:0032611,"mitochondrial complex 1 deficiency, nuclear type 6","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 6', 'MC1DN6']",0112066,618228,,,,,,,,,,
mondo:0032612,"mitochondrial complex 1 deficiency, nuclear type 7","['MC1DN7', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 7']",0112092,618229,,,,,,,,,,
mondo:0032613,"mitochondrial complex 1 deficiency, nuclear type 8","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 8', 'MC1DN8']",0112081,618230,,,,,,,,,,
mondo:0032614,"epidermodysplasia verruciformis, susceptibility to, 2","['epidermodysplasia verruciformis 2', 'EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 2', 'EV2']",,618231,,,,,,,,,,
mondo:0032615,"mitochondrial complex 1 deficiency, nuclear type 9","['MC1DN9', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 9']",0112073,618232,,,,,,,,,,
mondo:0032616,"mitochondrial complex 1 deficiency, nuclear type 10","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 10', 'MC1DN10']",0112075,618233,,,,,,,,,,
mondo:0032617,"mitochondrial complex 1 deficiency, nuclear type 11","['MC1DN11', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 11']",0112089,618234,,,,,,,,,,
mondo:0032618,"mitochondrial complex 1 deficiency, nuclear type 13","['MC1DN13', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 13']",0112076,618235,,,,,,,,,,
mondo:0032619,"mitochondrial complex 1 deficiency, nuclear type 14","['MC1DN14', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 14']",0112094,618236,,,,,,,,,,
mondo:0032620,"mitochondrial complex 1 deficiency, nuclear type 15","['MC1DN15', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 15']",0112077,618237,,,,,,,,,,
mondo:0032621,"mitochondrial complex 1 deficiency, nuclear type 16","['MC1DN16', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 16']",0112096,618238,,,,,,,,,,
mondo:0032622,"mitochondrial complex 1 deficiency, nuclear type 17","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 17', 'MC1DN17']",0112078,618239,,,,,,,,,,
mondo:0032623,"mitochondrial complex 1 deficiency, nuclear type 18","['MC1DN18', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 18']",0112070,618240,,,,,,,,,,
mondo:0032624,"mitochondrial complex 1 deficiency, nuclear type 19","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 19', 'MC1DN19']",0112085,618241,,,,,,,,,,
mondo:0032625,"mitochondrial complex 1 deficiency, nuclear type 21","['MC1DN21', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 21']",0112088,618242,,,,,,,,,,
mondo:0032626,"mitochondrial complex 1 deficiency, nuclear type 22","['MC1DN22', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 22']",0112069,618243,,,,,,,,,,
mondo:0032627,"mitochondrial complex 1 deficiency, nuclear type 23","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 23', 'MC1DN23']",0112087,618244,,,,,,,,,,
mondo:0032628,"mitochondrial complex 1 deficiency, nuclear type 24","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 24', 'MC1DN24']",0112079,618245,,,,,,,,,,
mondo:0032629,"mitochondrial complex 1 deficiency, nuclear type 25","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 25', 'MC1DN25']",0112067,618246,,,,,,,,,,
mondo:0032630,"mitochondrial complex 1 deficiency, nuclear type 26","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 26', 'MC1DN26']",0112086,618247,,,,,,,,,,
mondo:0032631,"mitochondrial complex 1 deficiency, nuclear type 27","['MC1DN27', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 27']",0112090,618248,,,,,,,,,,
mondo:0032632,"mitochondrial complex 1 deficiency, nuclear type 28","['MC1DN28', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 28']",0112095,618249,,,,,,,,,,
mondo:0032633,"mitochondrial complex 1 deficiency, nuclear type 29","['MC1DN29', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 29']",0112084,618250,,,,,,,,,,
mondo:0032634,"mitochondrial complex 1 deficiency, nuclear type 31","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 31', 'MC1DN31']",0112071,618251,,,,,,,,,,
mondo:0032635,"mitochondrial complex 1 deficiency, nuclear type 32","['MC1DN32', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 32']",0112080,618252,,,,,,,,,,
mondo:0032636,"mitochondrial complex 1 deficiency, nuclear type 33","['MC1DN33', 'MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 33']",0112097,618253,,,,,,,,,,
mondo:0032637,"ciliary dyskinesia, primary, 39","['CILIARY DYSKINESIA, PRIMARY, 39', 'CILD39', 'Ciliary Dyskinesia, Primary, 39, With or Without Situs Inversus']",0111854,618254,,,,,,,,,,
mondo:0032639,"hearing loss, autosomal recessive 112","['deafness, autosomal recessive 112', 'DFNB112']",0111637,618257,,,,,,,,,,
mondo:0032641,mirror movements 4,"['MRMV4', 'MIRROR MOVEMENTS 4']",,618264,,,,,,,,,,
mondo:0032642,"arthrogryposis, cleft palate, craniosynostosis, and impaired intellectual development","['ACCIID', 'ARTHROGRYPOSIS, CLEFT PALATE, CRANIOSYNOSTOSIS, AND IMPAIRED INTELLECTUAL DEVELOPMENT']",,618265,565858,,,,,,,,,
mondo:0032643,"pontocerebellar hypoplasia, type 12","['COASY-related pontocerebellar hypoplasia', 'PCH12', 'PONTOCEREBELLAR HYPOPLASIA, TYPE 12']",0112327,618266,611256,,,,,,,,,
mondo:0032644,"epidermodysplasia verruciformis, susceptibility to, 3","['EV3', 'EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 3', 'epidermodysplasia verruciformis 3']",,618267,,,,,,,,,,
mondo:0032645,trichohepatoneurodevelopmental syndrome,"['TRICHOHEPATONEURODEVELOPMENTAL SYNDROME', 'THNS']",,618268,,,,,,,,,,
mondo:0032646,congenital anomalies of kidney and urinary tract 3,"['CONGENITAL ANOMALIES OF KIDNEY AND URINARY TRACT 3', 'CAKUT3']",,618270,,,,,,,,,,
mondo:0032648,mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations,"['MEGA-CORPUS-CALLOSUM SYNDROME WITH CEREBELLAR HYPOPLASIA AND CORTICAL MALFORMATIONS', 'MCCCHCM']",0111403,618273,,,,,,,,,,
mondo:0032649,hypotrichosis 14,"['HYPOTRICHOSIS 14', 'HYPT14']",0080582,618275,,,,,,,,,,
mondo:0032650,"neurodegeneration, childhood-onset, with cerebellar atrophy","['NEURODEGENERATION, CHILDHOOD-ONSET, WITH CEREBELLAR ATROPHY', 'CONDCA']",,618276,,,,,,,,,,
mondo:0032651,"fibrosis, neurodegeneration, and cerebral angiomatosis","['FINCA', 'FINCA syndrome', 'FIBROSIS, NEURODEGENERATION, AND CEREBRAL ANGIOMATOSIS']",,618278,,,,,,,,,,
mondo:0032653,cardiac-urogenital syndrome,"['CUGS', 'CARDIAC-UROGENITAL SYNDROME']",,618280,647811,,,,,,,,,
mondo:0032654,"hyper-IgE recurrent infection syndrome 3, autosomal recessive","['HYPER-IgE RECURRENT INFECTION SYNDROME 3, AUTOSOMAL RECESSIVE', 'HIES3']",0080595,618282,,,,,,,,,,
mondo:0032655,visual impairment and progressive phthisis bulbi,"['VIPB', 'VISUAL IMPAIRMENT AND PROGRESSIVE PHTHISIS BULBI']",0070356,618283,,,,,,,,,,
mondo:0032656,"microcephaly, cataracts, impaired intellectual development, and dystonia with abnormal striatum","['MICROCEPHALY, CATARACTS, IMPAIRED INTELLECTUAL DEVELOPMENT, AND DYSTONIA WITH ABNORMAL STRIATUM', 'MCIDDS']",,618284,,,,,,,,,,
mondo:0032657,"developmental and epileptic encephalopathy, 69","['EIEE69', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 69', 'DEE69', 'epileptic encephalopathy, early infantile, 69', 'developmental and epileptic encephalopathy 69']",0112205,618285,,,,,,,,,,
mondo:0032658,"macrocephaly, acquired, with impaired intellectual development","['Macrocephaly, Acquired, With Mental Retardation', 'MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT', 'MACID']",,618286,,,,,,,,,,
mondo:0032659,"mucocutaneous ulceration, chronic","['CMCU', 'MUCOCUTANEOUS ULCERATION, CHRONIC']",,618287,,,,,,,,,,
mondo:0032660,"spinal muscular atrophy, lower extremity-predominant, 2b, prenatal onset, autosomal dominant","['SPINAL MUSCULAR ATROPHY, LOWER EXTREMITY-PREDOMINANT, 2B, PRENATAL ONSET, AUTOSOMAL DOMINANT', 'spinal muscular atrophy, lower extremity-predominant, 2B, autosomal dominant', 'SMALED2B']",0070350,618291,,,,,,,,,,
mondo:0032661,"neurodevelopmental disorder with impaired intellectual development, hypotonia, and ataxia","['NEURODEVELOPMENTAL DISORDER WITH IMPAIRED INTELLECTUAL DEVELOPMENT, HYPOTONIA, AND ATAXIA', 'NEDIDHA']",,618292,,,,,,,,,,
mondo:0032662,"intellectual developmental disorder, autosomal recessive 67","['Mental Retardation, Autosomal Recessive 67', 'MRT67', 'INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 67']",0081228,618295,,,,,,,,,,
mondo:0032663,"developmental and epileptic encephalopathy, 70","['DEE70', 'epileptic encephalopathy, early infantile, 70', 'EIEE70', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 70', 'developmental and epileptic encephalopathy 70']",0112206,618298,,,,,,,,,,
mondo:0032664,"ciliary dyskinesia, primary, 40","['CILIARY DYSKINESIA, PRIMARY, 40', 'Ciliary Dyskinesia, Primary, 40, With or Without Situs Inversus', 'CILD40']",0111853,618300,,,,,,,,,,
mondo:0032665,"intellectual developmental disorder, autosomal recessive 68","['MRT68', 'Mental Retardation, Autosomal Recessive 68', 'INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 68']",0081229,618302,,,,,,,,,,
mondo:0032666,"epidermodysplasia verruciformis, susceptibility to, 4","['EV4', 'EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 4']",,618307,,,,C176608,,,,,,
mondo:0032667,"epidermodysplasia verruciformis, susceptibility to, 5","['EV5', 'EPIDERMODYSPLASIA VERRUCIFORMIS, SUSCEPTIBILITY TO, 5']",,618309,,,,,,,,,,
mondo:0032668,Diamond-Blackfan anemia 18,"['DBA18', 'DIAMOND-BLACKFAN ANEMIA 18']",0111896,618310,,,,,,,,,,
mondo:0032669,Diamond-Blackfan anemia 19,"['DBA19', 'DIAMOND-BLACKFAN ANEMIA 19']",0111886,618312,,,,,,,,,,
mondo:0032670,Diamond-Blackfan anemia 20,"['DIAMOND-BLACKFAN ANEMIA 20', 'DBA20']",0111891,618313,,,,,,,,,,
mondo:0032672,intellectual developmental disorder with cardiac defects and dysmorphic facies,"['IDDCDF', 'INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC DEFECTS AND DYSMORPHIC FACIES']",,618316,562569,,,,,,,,,
mondo:0032673,"basal ganglia calcification, idiopathic, 7, autosomal recessive","['IBGC7', 'BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 7, AUTOSOMAL RECESSIVE']",,618317,,,,,,,,,,
mondo:0032675,"myasthenic syndrome, congenital, 25, presynaptic","['myasthenic syndrome, congenital, 25', 'MYASTHENIC SYNDROME, CONGENITAL, 25, PRESYNAPTIC', 'CMS25']",,618323,,,,,,,,,,
mondo:0032677,lissencephaly 9 with complex brainstem malformation,"['LISSENCEPHALY 9 WITH COMPLEX BRAINSTEM MALFORMATION', 'LIS9']",0112228,618325,572013,,,,,,,,,
mondo:0032678,"developmental and epileptic encephalopathy, 71","['Glutaminase Deficiency With Neonatal Epileptic Encephalopathy', 'DEE71', 'developmental and epileptic encephalopathy 71', 'EIEE71', 'epileptic encephalopathy, early infantile, 71', 'neonatal epileptic encephalopathy due to glutaminase deficiency']",0112207,618328,557064,,,,,,,,,
mondo:0032679,combined oxidative phosphorylation deficiency 37,"['COXPD37', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 37']",0111499,618329,,,,,,,,,,
mondo:0032680,global developmental delay with or without impaired intellectual development,"['GLOBAL DEVELOPMENTAL DELAY WITH OR WITHOUT IMPAIRED INTELLECTUAL DEVELOPMENT', 'GDDI']",,618330,,,,,,,,,,
mondo:0032681,"encephalopathy, progressive, early-onset, with episodic rhabdomyolysis","['PEERB', 'ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH EPISODIC RHABDOMYOLYSIS']",,618331,,,,,,,,,,
mondo:0032684,"intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, genital anomalies, and immunodeficiency","['IMAGE-I syndrome', 'INTRAUTERINE GROWTH RETARDATION, METAPHYSEAL DYSPLASIA, ADRENAL HYPOPLASIA CONGENITA, GENITAL ANOMALIES, AND IMMUNODEFICIENCY', 'Imagei Syndrome', 'IMAGEI']",,618336,,,,,,,,,,
mondo:0032685,"infantile cataract, skin abnormalities, glutamate excess, and impaired intellectual development","['INFANTILE CATARACT, SKIN ABNORMALITIES, GLUTAMATE EXCESS, AND IMPAIRED INTELLECTUAL DEVELOPMENT', 'CASGID']",,618339,,,,,,,,,,
mondo:0032686,spermatogenic failure 35,"['SPGF35', 'SPERMATOGENIC FAILURE 35']",0111914,618341,,,,,,,,,,
mondo:0032687,"intellectual developmental disorder with abnormal behavior, microcephaly, and short stature","['IDDABS', 'INTELLECTUAL DEVELOPMENTAL DISORDER WITH ABNORMAL BEHAVIOR, MICROCEPHALY, AND SHORT STATURE']",0081265,618342,,,,,,,,,,
mondo:0032688,polymicrogyria with or without vascular-type Ehlers-Danlos syndrome,"['PMGEDSV', 'polymicrogyria with or without vascular-type EDS', 'vascular Ehlers-Danlos-polymicrogyria syndrome', 'POLYMICROGYRIA WITH OR WITHOUT VASCULAR-TYPE EHLERS-DANLOS SYNDROME']",,618343,636941,,,,,,,,,
mondo:0032689,retinitis pigmentosa 85,"['RETINITIS PIGMENTOSA 85', 'RP85']",0112142,618345,,,,,,,,,,
mondo:0032690,"microcephaly, growth deficiency, seizures, and brain malformations","['MIGSB', 'MICROCEPHALY, GROWTH DEFICIENCY, SEIZURES, AND BRAIN MALFORMATIONS']",0081051,618346,,,,,,,,,,
mondo:0032691,Galloway-Mowat syndrome 6,"['GAMOS6', 'GALLOWAY-MOWAT SYNDROME 6']",,618347,,,,,,,,,,
mondo:0032692,Galloway-Mowat syndrome 7,"['GALLOWAY-MOWAT SYNDROME 7', 'GAMOS7']",,618348,,,,,,,,,,
mondo:0032693,Galloway-Mowat syndrome 8,"['GAMOS8', 'GALLOWAY-MOWAT SYNDROME 8']",,618349,,,,,,,,,,
mondo:0032694,"microcephaly 25, primary, autosomal recessive","['MCPH25', 'MICROCEPHALY 25, PRIMARY, AUTOSOMAL RECESSIVE']",,618351,,,,,,,,,,
mondo:0032696,oocyte maturation defect 6,"['OOCYTE MATURATION DEFECT 6', 'OOMD6']",,618353,,,,,,,,,,
mondo:0032697,neurodevelopmental disorder and language delay with or without structural brain abnormalities,"['NEDLBA', 'NEURODEVELOPMENTAL DISORDER AND LANGUAGE DELAY WITH OR WITHOUT STRUCTURAL BRAIN ABNORMALITIES']",,618354,,,,,,,,,,
mondo:0032698,neurodevelopmental disorder with central and peripheral motor dysfunction,"['NEURODEVELOPMENTAL DISORDER WITH CENTRAL AND PERIPHERAL MOTOR DYSFUNCTION', 'NEDCPMD']",,618356,,,,,,,,,,
mondo:0032699,"epilepsy, idiopathic generalized, susceptibility to, 15","['EPILEPSY, IDIOPATHIC GENERALIZED, SUSCEPTIBILITY TO, 15', 'EIG15']",0111316,618357,,,,,,,,,,
mondo:0032702,Coffin-Siris syndrome 8,"['CSS8', 'SMARCC2-related BAFopathy', 'COFFIN-SIRIS SYNDROME 8']",0112367,618362,,,,,,,,,,
mondo:0032703,"short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis","['SHORT STATURE, AMELOGENESIS IMPERFECTA, AND SKELETAL DYSPLASIA WITH SCOLIOSIS', 'SSASKS']",,618363,,,,,,,,,,
mondo:0032705,"neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination","['NEDMEHM', 'NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND HYPOMYELINATION', 'MTHFS-related developmental delay-microcephaly-short stature-epilepsy syndrome']",,618367,597874,,,,,,,,,
mondo:0032706,"spinocerebellar ataxia, autosomal recessive 27","['SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 27', 'SCAR27']",0111616,618369,,,,,,,,,,
mondo:0032707,turnpenny-fry syndrome,"['Neurocardioskeletal Syndrome', 'TURNPENNY-FRY SYNDROME', 'TPFS']",,618371,,,,,,,,,,
mondo:0032710,"developmental and epileptic encephalopathy, 72","['EIEE72', 'DEE72', 'epileptic encephalopathy, early infantile, 72', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 72', 'developmental and epileptic encephalopathy 72']",0112208,618374,,,,,,,,,,
mondo:0032712,combined oxidative phosphorylation deficiency 38,"['COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 38', 'COXPD38']",0111466,618378,,,,,,,,,,
mondo:0032714,"facial dysmorphism, hypertrichosis, epilepsy, intellectual/developmental delay, and gingival overgrowth syndrome","['FACIAL DYSMORPHISM, HYPERTRICHOSIS, EPILEPSY, INTELLECTUAL/DEVELOPMENTAL DELAY, AND GINGIVAL OVERGROWTH SYNDROME', 'FHEIG']",,618381,598603,,,,,,,,,
mondo:0032715,"intellectual developmental disorder, autosomal recessive 69","['INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 69', 'Mental Retardation, Autosomal Recessive 69', 'MRT69']",0081230,618383,,,,,,,,,,
mondo:0032716,"leukoencephalopathy, acute reversible, with increased urinary alpha-ketoglutarate","['LEUKOENCEPHALOPATHY, ACUTE REVERSIBLE, WITH INCREASED URINARY ALPHA-KETOGLUTARATE', 'acute reversible leukoencephalopathy with increased urinary alpha-ketoglutarate', 'ARLIAK', 'acute reversible leukoencephalopathy due to sodium-dependent dicarboxylate transporter deficiency', 'acute reversible leukoencephalopathy due to SLC13A3 deficiency']",,618384,615964,,,,,,,,,
mondo:0032717,"amelogenesis imperfecta, type 3c","['AI3C', 'Amelogenesis Imperfecta, Hypocalcification Type, Autosomal Recessive', 'AMELOGENESIS IMPERFECTA, TYPE IIIC']",0111722,618386,,,,,,,,,,
mondo:0032721,"spondyloepiphyseal dysplasia, kondo-fu type","['SPONDYLOEPIPHYSEAL DYSPLASIA, KONDO-FU TYPE', 'Sed With Elevated Blood Lysosomal Enzymes', 'SEDKF']",0112283,618392,,,,,,,,,,
mondo:0032723,immunodeficiency 60,"['IMMUNODEFICIENCY 60', 'Immunodeficiency and Autoimmunity, Bach2-Related', 'immunodeficiency 60 and autoimmunity', 'IMD60']",0111954,618394,,,,,,,,,,
mondo:0032724,"spondyloepimetaphyseal dysplasia with joint laxity, type 3","['spondyloepimetaphyseal dysplasia with joint laxity, EXOC6b type', 'SPONDYLOEPIMETAPHYSEAL DYSPLASIA WITH JOINT LAXITY, TYPE 3', 'SEMDJL3']",0112200,618395,642085,,,,,,,,,
mondo:0032725,"developmental and epileptic encephalopathy, 74","['EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 74', 'epileptic encephalopathy, early infantile, 74', 'developmental and epileptic encephalopathy 74', 'EIEE74', 'DEE74']",0112210,618396,,,,,,,,,,
mondo:0032726,combined oxidative phosphorylation deficiency 39,"['COXPD39', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 39']",0111475,618397,565624,,,,,,,,,
mondo:0032728,"Charcot-Marie-Tooth disease, axonal, type 2EE","['CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2EE', 'Charcot-Marie-Tooth Neuropathy, Type 2Ee', 'CMT2EE']",0111559,618400,,,,,,,,,,
mondo:0032729,"intellectual developmental disorder, autosomal recessive 70","['MRT70', 'Mental Retardation, Autosomal Recessive 70', 'INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 70']",0081231,618402,,,,,,,,,,
mondo:0032730,"leukodystrophy, hypomyelinating, 18","['HLD18', 'LEUKODYSTROPHY, HYPOMYELINATING, 18']",0070399,618404,,,,,,,,,,
mondo:0032732,"hearing loss, autosomal recessive 113","['DFNB113', 'deafness, autosomal recessive 113']",0111636,618410,,,,,,,,,,
mondo:0032733,"global developmental delay, progressive ataxia, and elevated glutamine","['Glutaminase Deficiency With Impaired Intellectual Development and Progressive Ataxia', 'GDPAG', 'GLOBAL DEVELOPMENTAL DELAY, PROGRESSIVE ATAXIA, AND ELEVATED GLUTAMINE']",,618412,,,,,,,,,,
mondo:0032735,cataract 48,"['CATARACT 48', 'CTRCT48']",0070354,618415,,,,,,,,,,
mondo:0032736,"metabolic crises, recurrent, with variable encephalomyopathic features and neurologic regression","['METABOLIC CRISES, RECURRENT, WITH VARIABLE ENCEPHALOMYOPATHIC FEATURES AND NEUROLOGIC REGRESSION', 'MECREN']",,618416,,,,,,,,,,
mondo:0032737,"spastic paraplegia 80, autosomal dominant","['SPASTIC PARAPLEGIA 80, AUTOSOMAL DOMINANT', 'SPG80']",0112341,618418,,,,,,,,,,
mondo:0032738,"gonadal dysgenesis, dysmorphic facies, retinal dystrophy, and myopathy","['agonadism, 46,XY, with mental retardation, short stature, retarded bone age, and multiple extragenital malformations', 'GDRM', 'Kennerknecht syndrome', 'KENNERKNECHT syndrome', 'agonadism, 46,XY, with intellectual disability, short stature, retarded bone age, and multiple extragenital malformations', 'GONADAL DYSGENESIS, DYSMORPHIC FACIES, RETINAL DYSTROPHY, AND MYOPATHY']",,618419,,C1833162,,,,,,,,
mondo:0032739,spermatogenic failure 36,"['SPGF36', 'SPERMATOGENIC FAILURE 36']",0111921,618420,,,,,,,,,,
mondo:0032740,"hearing loss, autosomal recessive 100","['DFNB100', 'deafness, autosomal recessive 100']",0111638,618422,,,,,,,,,,
mondo:0032741,neurodevelopmental disorder with impaired speech and hyperkinetic movements,"['NEDISHM', 'NEURODEVELOPMENTAL DISORDER WITH IMPAIRED SPEECH AND HYPERKINETIC MOVEMENTS']",,618425,,,,,,,,,,
mondo:0032742,"encephalopathy, acute, infection-induced, susceptibility to, 9","['ENCEPHALOPATHY, ACUTE, INFECTION-INDUCED, SUSCEPTIBILITY TO, 9', 'IIAE9']",,618426,,,,,,,,,,
mondo:0032744,spermatogenic failure 37,"['SPERMATOGENIC FAILURE 37', 'SPGF37']",0111927,618429,,,,,,,,,,
mondo:0032745,developmental delay with variable intellectual impairment and behavioral abnormalities,"['DEVELOPMENTAL DELAY WITH VARIABLE INTELLECTUAL IMPAIRMENT AND BEHAVIORAL ABNORMALITIES', 'DDVIBA']",,618430,,,,,,,,,,
mondo:0032746,"hydatidiform mole, recurrent, 3","['HYDM3', 'HYDATIDIFORM MOLE, RECURRENT, 3']",,618431,,,,,,,,,,
mondo:0032747,"hydatidiform mole, recurrent, 4","['HYDATIDIFORM MOLE, RECURRENT, 4', 'HYDM4']",,618432,,,,,,,,,,
mondo:0032748,spermatogenic failure 38,"['SPGF38', 'SPERMATOGENIC FAILURE 38']",0111919,618433,,,,,,,,,,
mondo:0032749,"hearing loss, autosomal recessive 94","['deafness, autosomal recessive 94', 'DFNB94']",0111641,618434,,,,,,,,,,
mondo:0032750,"arthrogryposis, distal, type 2B2","['DA2B2', 'arthrogryposis, distal, type 2B2']",0111601,618435,,,,,,,,,,
mondo:0032751,"arthrogryposis, distal, type 2B3","['distal arthrogryposis type 2B3 (Sheldon-Hall)', 'arthrogryposis, distal, type 2B3 (Sheldon-Hall)', 'arthrogryposis, distal, type 2B3', 'DA2B3']",0111602,618436,,,,,,,,,,
mondo:0032752,"developmental and epileptic encephalopathy, 75","['epileptic encephalopathy, early infantile, 75', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 75', 'developmental and epileptic encephalopathy 75', 'DEE75', 'EIEE75']",0112211,618437,,,,,,,,,,
mondo:0032753,"spastic ataxia 9, autosomal recessive","['SPASTIC ATAXIA 9, AUTOSOMAL RECESSIVE', 'SPAX9']",,618438,,,,,,,,,,
mondo:0032755,neurodevelopmental disorder with or without variable brain abnormalities; NEDBA,"['NEDBA', 'NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT VARIABLE BRAIN ABNORMALITIES']",,618443,,,,,,,,,,
mondo:0032756,long qt syndrome 8,"['LQT8', 'LONG QT SYNDROME 8']",,618447,,,,,,,,,,
mondo:0032757,"ciliary dyskinesia, primary, 41","['CILIARY DYSKINESIA, PRIMARY, 41', 'CILD41']",0111858,618449,,,,,,,,,,
mondo:0032758,"neurodegeneration, early-onset, with choreoathetoid movements and microcytic anemia","['NDCAMA', 'NEURODEGENERATION, EARLY-ONSET, WITH CHOREOATHETOID MOVEMENTS AND MICROCYTIC ANEMIA']",,618451,,,,,,,,,,
mondo:0032759,intellectual developmental disorder with short stature and variable skeletal anomalies,"['IDDSSA', 'INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND VARIABLE SKELETAL ANOMALIES']",,618453,,,,,,,,,,
mondo:0032760,developmental delay with or without dysmorphic facies and autism,"['DEVELOPMENTAL DELAY WITH OR WITHOUT DYSMORPHIC FACIES AND AUTISM', 'DEDDFA']",,618454,,,,,,,,,,
mondo:0032761,"hearing loss, autosomal recessive 114","['DFNB114', 'deafness, autosomal recessive 114']",0111642,618456,,,,,,,,,,
mondo:0032762,"hearing loss, autosomal recessive 115","['deafness, autosomal recessive 115', 'DFNB115']",0111643,618457,,,,,,,,,,
mondo:0032763,immunodeficiency 62,"['IMMUNODEFICIENCY 62', 'IMD62']",0111991,618459,,,,,,,,,,
mondo:0032764,Khan-Khan-Katsanis syndrome,"['KHAN-KHAN-KATSANIS SYNDROME', '3K Syndrome', '3KS']",,618460,,,,,,,,,,
mondo:0032765,"bleeding disorder, platelet-type, 22","['BDPLT22', 'BLEEDING DISORDER, PLATELET-TYPE, 22']",,618462,,,,,,,,,,
mondo:0032766,"hypoalphalipoproteinemia, primary, 2","['hypoalphalipoproteinemia, primary, 2, with or without corneal clouding', 'High Density Lipoprotein Deficiency', 'HYPOALPHALIPOPROTEINEMIA, PRIMARY, 2', 'Apolipoprotein A-I Deficiency', 'ApoA-I and apoC-III deficiency, combined']",0080958,618463,,,,,,,,,,
mondo:0032767,paragangliomas 6,"['PGL6', 'PARAGANGLIOMAS 6']",,618464,,,,,,,,,,
mondo:0032768,"developmental and epileptic encephalopathy, 76","['developmental and epileptic encephalopathy 76', 'Developmental Delay, Epileptic Encephalopathy, Cerebral Atrophy, and Abnormal Myelination', 'epileptic encephalopathy, early infantile, 76', 'EIEE76', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 76', 'DEE76']",0112212,618468,,,,,,,,,,
mondo:0032770,intellectual developmental disorder with severe speech and ambulation defects,"['ACTL6B-related BAFopathy', 'IDDSSAD', 'INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEVERE SPEECH AND AMBULATION DEFECTS']",,618470,,,,,,,,,,
mondo:0032771,paragangliomas 7,"['PARAGANGLIOMAS 7', 'PGL7']",,618475,,,,,,,,,,
mondo:0032772,"brain abnormalities, neurodegeneration, and dysosteosclerosis","['BRAIN ABNORMALITIES, NEURODEGENERATION, AND DYSOSTEOSCLEROSIS', 'BANDDOS']",,618476,,,,,,,,,,
mondo:0032773,uridine-cytidineuria,"['URIDINE-CYTIDINEURIA', 'URCTU', 'uridine-cytidineuria']",,618477,,,,,,,,,,
mondo:0032774,"cerebellar, ocular, craniofacial, and genital syndrome","['CEREBELLAR, OCULAR, CRANIOFACIAL, AND GENITAL SYNDROME', 'COFG']",,618479,,,,,,,,,,
mondo:0032775,neurodevelopmental disorder with seizures and speech and walking impairment,"['NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND SPEECH AND WALKING IMPAIRMENT', 'NEDSSWI']",,618480,,,,,,,,,,
mondo:0032776,"hearing loss, autosomal recessive 99","['deafness, autosomal recessive 99', 'DFNB99']",0111634,618481,,,,,,,,,,
mondo:0032777,"generalized epilepsy with febrile seizures plus, type 10","['GEFSP10', 'GENERALIZED EPILEPSY WITH FEBRILE SEIZURES PLUS, TYPE 10', 'Gefs+, Type 10']",0111296,618482,,,,,,,,,,
mondo:0032778,"arthrogryposis multiplex congenita 3, myogenic type","['arthrogryposis multiplex congenita, myogenic type', 'AMCM']",0080979,618484,,,,,,,,,,
mondo:0032779,neurodevelopmental disorder with microcephaly and structural brain anomalies,"['NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND STRUCTURAL BRAIN ANOMALIES', 'NEDMIBA']",,618492,,,,,,,,,,
mondo:0032780,"hypotonia, hypoventilation, impaired intellectual development, dysautonomia, epilepsy, and eye abnormalities","['HIDEA', 'HYPOTONIA, HYPOVENTILATION, IMPAIRED INTELLECTUAL DEVELOPMENT, DYSAUTONOMIA, EPILEPSY, AND EYE ABNORMALITIES']",,618493,,,,,,,,,,
mondo:0032781,"congenital hypotonia, epilepsy, developmental delay, and digital anomalies","['CHEDDA', 'CONGENITAL HYPOTONIA, EPILEPSY, DEVELOPMENTAL DELAY, AND DIGITAL ANOMALIES']",,618494,,,,,,,,,,
mondo:0032782,immunodeficiency 63 with lymphoproliferation and autoimmunity,"['Interleukin 2 Receptor, Beta, Deficiency of', 'IMMUNODEFICIENCY 63 WITH LYMPHOPROLIFERATION AND AUTOIMMUNITY', 'IMD63', 'Cd122 Deficiency', 'Il2Rb Deficiency']",0111997,618495,,,,,,,,,,
mondo:0032783,aortic valve disease 3,"['AORTIC VALVE DISEASE 3', 'AOVD3']",0080977,618496,,,,,,,,,,
mondo:0032784,neurodevelopmental disorder with seizures and nonepileptic hyperkinetic movements,"['NEDNEH', 'NEURODEVELOPMENTAL DISORDER WITH SEIZURES AND NONEPILEPTIC HYPERKINETIC MOVEMENTS']",,618497,,,,,,,,,,
mondo:0032785,"polydactyly, postaxial, type a10","['POLYDACTYLY, POSTAXIAL, TYPE A10', 'PAPA10']",,618498,,,,,,,,,,
mondo:0032786,Noonan syndrome 11,"['NOONAN SYNDROME 11', 'NS11']",0112169,618499,,,,C177119,,,,,,
mondo:0032787,holoprosencephaly 12 with or without pancreatic agenesis,"['HPE12', 'HOLOPROSENCEPHALY 12 WITH OR WITHOUT PANCREATIC AGENESIS', 'holoprosencephaly 12, with or without pancreatic agenesis']",,618500,,,,,,,,,,
mondo:0032788,cerebellar atrophy with seizures and variable developmental delay,"['CEREBELLAR ATROPHY WITH SEIZURES AND VARIABLE DEVELOPMENTAL DELAY', 'CASVDD']",,618501,,,,,,,,,,
mondo:0032789,"intellectual developmental disorder, autosomal recessive 71","['MRT71', 'INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 71', 'Mental Retardation, Autosomal Recessive 71']",0081232,618504,,,,,,,,,,
mondo:0032790,neurodevelopmental disorder with coarse facies and mild distal skeletal abnormalities,"['NEDCFSA', 'NEURODEVELOPMENTAL DISORDER WITH COARSE FACIES AND MILD DISTAL SKELETAL ABNORMALITIES']",,618505,,,,,,,,,,
mondo:0032791,Coffin-Siris syndrome 10,"['COFFIN-SIRIS SYNDROME 10', 'CSS10']",0112371,618506,,,,,,,,,,
mondo:0032792,"neuropathy, hereditary motor and sensory, type VIc, with optic atrophy","['HMSN6C', 'CMT 6C', 'CMT6C', 'Charcot-Marie-Tooth Disease, Type 6C', 'HMSN 6C', 'neuropathy, hereditary motor and sensory, type VIc, with optic atrophy']",,618511,,,,,,,,,,
mondo:0032793,O^Donnell-Luria-Rodan syndrome,"['O^Donnell-Luria-Rodan syndrome', 'ODLURO']",,618512,,,,,,,,,,
mondo:0032794,leber congenital amaurosis 19,"['LCA19', 'LEBER CONGENITAL AMAUROSIS 19']",0081169,618513,,,,,,,,,,
mondo:0032795,intellectual developmental disorder 59,"['INTELLECTUAL DEVELOPMENTAL DISORDER 59', 'MRD59', 'Mental Retardation, Autosomal Dominant 59']",,618522,,,,,,,,,,
mondo:0032796,"hyper-IgE recurrent infection syndrome 4, autosomal recessive","['hyper-IgE recurrent infection syndrome 4B, autosomal recessive', 'HYPER-IgE RECURRENT INFECTION SYNDROME 4, AUTOSOMAL RECESSIVE', 'HIES4']",0080596,618523,,,,,,,,,,
mondo:0032797,"myopathy, congenital, with tremor","['MYOPATHY, CONGENITAL, WITH TREMOR', 'MYOTREM', 'Myogenic Tremor']",0081348,618524,,,,,,,,,,
mondo:0032798,"ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facial features","['ichthyotic keratoderma, spasticity, hypomyelination, and dysmorphic facies', 'ICHTHYOTIC KERATODERMA, SPASTICITY, HYPOMYELINATION, AND DYSMORPHIC FACIAL FEATURES', 'IKSHD']",,618527,,,,,,,,,,
mondo:0032799,mitochondrial DNA depletion syndrome 16 (hepatic type),"['MITOCHONDRIAL DNA DEPLETION SYNDROME 16 (HEPATIC TYPE)', 'MTDPS16']",,618528,,,,,,,,,,
mondo:0032800,"robinow syndrome, autosomal recessive 2","['RRS2', 'ROBINOW SYNDROME, AUTOSOMAL RECESSIVE 2']",,618529,,,,,,,,,,
mondo:0032801,erythrokeratodermia variabilis et progressiva 6,"['EKVP6', 'ERYTHROKERATODERMIA VARIABILIS ET PROGRESSIVA 6']",0080766,618531,,,,,,,,,,
mondo:0032802,"hearing loss, autosomal dominant 37","['DEAFNESS, AUTOSOMAL DOMINANT 37', 'DFNA37', 'deafness, autosomal dominant 37']",,618533,,,,,,,,,,
mondo:0032803,immunodeficiency 64,"['IMD64', 'IMMUNODEFICIENCY 64']",0111980,618534,,,,,,,,,,
mondo:0032804,"ectodermal dysplasia 15, hypohidrotic/hair type","['ECTD15', 'ECTODERMAL DYSPLASIA 15, HYPOHIDROTIC/HAIR TYPE']",0111651,618535,,,,,,,,,,
mondo:0032805,"hypopigmentation, organomegaly, and delayed myelination and development","['HOD', 'HYPOPIGMENTATION, ORGANOMEGALY, AND DELAYED MYELINATION AND DEVELOPMENT']",,618541,,,,,,,,,,
mondo:0032806,"trichothiodystrophy 7, nonphotosensitive","['TRICHOTHIODYSTROPHY 7, NONPHOTOSENSITIVE', 'TTD7']",0111870,618546,,,,C173102,,,,,,
mondo:0032807,neurodevelopmental disorder with visual defects and brain anomalies,"['NEDVIBA', 'NEURODEVELOPMENTAL DISORDER WITH VISUAL DEFECTS AND BRAIN ANOMALIES']",,618547,,,,,,,,,,
mondo:0032808,"developmental and epileptic encephalopathy, 77","['EIEE77', 'multiple congenital anomalies-hypotonia-seizures syndrome 4', 'glycosylphosphatidylinositol biosynthesis defect 19', 'DEE77', 'epileptic encephalopathy, early infantile, 77']",0112213,618548,,,,,,,,,,
mondo:0032809,"hepatitis, fulminant viral, susceptibility to","['HEPATITIS, FULMINANT VIRAL, SUSCEPTIBILITY TO', 'FVH']",,618549,,,,,,,,,,
mondo:0032810,oocyte maturation defect 7,"['OOCYTE MATURATION DEFECT 7', 'OOMD7']",,618550,,,,,,,,,,
mondo:0032811,"night blindness, congenital stationary, type1i","['NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE1I', 'CSNB1I', 'night blindness, congenital stationary, type 1I']",,618555,,,,,,,,,,
mondo:0032812,"developmental and epileptic encephalopathy, 78","['DEE78', 'epileptic encephalopathy, early infantile, 78', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 78', 'EIEE78', 'developmental and epileptic encephalopathy 78']",0112214,618557,,,,,,,,,,
mondo:0032813,"developmental and epileptic encephalopathy, 79","['developmental and epileptic encephalopathy 79', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 79', 'EIEE79', 'DEE79', 'epileptic encephalopathy, early infantile, 79']",0112215,618559,,,,,,,,,,
mondo:0032814,"microangiopathy and leukoencephalopathy, pontine, autosomal dominant","['Dementia, Hereditary Multi-Infarct, Swedish Type', 'MICROANGIOPATHY AND LEUKOENCEPHALOPATHY, PONTINE, AUTOSOMAL DOMINANT', 'PADMAL']",,618564,,,,,,,,,,
mondo:0032815,mitochondrial DNA depletion syndrome 17,"['MTDPS17', 'MITOCHONDRIAL DNA DEPLETION SYNDROME 17']",,618567,,,,,,,,,,
mondo:0032816,"neurodevelopmental disorder with ataxia, hypotonia, and microcephaly","['NEURODEVELOPMENTAL DISORDER WITH ATAXIA, HYPOTONIA, AND MICROCEPHALY', 'NEDAHM']",,618569,,,,,,,,,,
mondo:0032817,"neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies","['NDCAGF', 'NEURODEVELOPMENTAL DISORDER WITH CATARACTS, POOR GROWTH, AND DYSMORPHIC FACIES']",0070346,618571,,,,,,,,,,
mondo:0032818,neurodevelopmental disorder with cerebellar hypoplasia and spasticity,"['NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR HYPOPLASIA AND SPASTICITY', 'NEDCHS']",,618572,,,,,,,,,,
mondo:0032819,"hypothyroidism, congenital, nongoitrous, 7","['resistance to thyrotropin-releasing hormone syndrome', 'thyrotropin-releasing hormone resistance, generalised', 'central hypothyroidism due to TRH receptor deficiency', 'HYPOTHYROIDISM, CONGENITAL, NONGOITROUS, 7', 'CHNG7', 'TRH resistance syndrome', 'thyrotropin-releasing hormone resistance, generalized']",0111836,618573,99832,CN207394,,,,,,,,
mondo:0032820,neurodevelopmental disorder with structural brain anomalies and dysmorphic facies,"['NEURODEVELOPMENTAL DISORDER WITH STRUCTURAL BRAIN ANOMALIES AND DYSMORPHIC FACIES', 'NEDBAF']",,618577,,,,,,,,,,
mondo:0032821,"myopathy, congenital, progressive, with scoliosis","['MYOSCO', 'myopathy, congenital, progressive, with scoliosis']",0081351,618578,,,,,,,,,,
mondo:0032822,"developmental and epileptic encephalopathy, 80","['EIEE80', 'DEE80', 'developmental and epileptic encephalopathy 80', 'epileptic encephalopathy, early infantile, 80', 'Glycosylphosphatidylinositol Biosynthesis Defect 20', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 80']",0112216,618580,,,,,,,,,,
mondo:0032823,intellectual developmental disorder 60 with seizures,"['MRD60', 'Mental Retardation, Autosomal Dominant 60, With Seizures', 'INTELLECTUAL DEVELOPMENTAL DISORDER 60 WITH SEIZURES']",,618587,,,,,,,,,,
mondo:0032824,glycosylphosphatidylinositol biosynthesis defect 21,"['GLYCOSYLPHOSPHATIDYLINOSITOL BIOSYNTHESIS DEFECT 21', 'GPIBD21', 'Neurodevelopmental Disorder With Brain Anomalies, Seizures, and Scoliosis']",,618590,,,,,,,,,,
mondo:0032826,"nephrotic syndrome, type 21","['NPHS21', 'NEPHROTIC SYNDROME, TYPE 21']",0112267,618594,,,,,,,,,,
mondo:0032827,"epilepsy, idiopathic generalized, susceptibility to, 16",['EIG16'],,618596,,,,,,,,,,
mondo:0032828,"spastic tetraplegia and axial hypotonia, progressive","['SPASTIC TETRAPLEGIA AND AXIAL HYPOTONIA, PROGRESSIVE', 'STAHP', 'Sod1 Deficiency, Autosomal Recessive']",,618598,,,,,,,,,,
mondo:0032829,neurodevelopmental disorder with hypotonia and variable intellectual and behavioral abnormalities,"['NEDHIB', 'NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND VARIABLE INTELLECTUAL AND BEHAVIORAL ABNORMALITIES']",,618603,,,,,,,,,,
mondo:0032830,snijders blok-fisher syndrome,"['SNIBFIS', 'SNIJDERS BLOK-FISHER SYNDROME']",,618604,,,,,,,,,,
mondo:0032831,"pontocerebellar hypoplasia, type 13","['PCH13', 'PONTOCEREBELLAR HYPOPLASIA, TYPE 13']",0112332,618606,613267,,,,,,,,,
mondo:0032832,"intellectual developmental disorder with nasal speech, dysmorphic facies, and variable skeletal anomalies","['INTELLECTUAL DEVELOPMENTAL DISORDER WITH NASAL SPEECH, DYSMORPHIC FACIES, AND VARIABLE SKELETAL ANOMALIES', 'IDNADFS', 'Chromosome 12Q15 Deletion Syndrome']",,618608,,,,,,,,,,
mondo:0032833,"lower urinary tract obstruction, congenital","['LUTO', 'LOWER URINARY TRACT OBSTRUCTION, CONGENITAL']",,618612,,,,,,,,,,
mondo:0032834,retinitis pigmentosa 86,"['RETINITIS PIGMENTOSA 86', 'RP86']",0112143,618613,,,,,,,,,,
mondo:0032835,"spondyloepiphyseal dysplasia, nishimura type","['SEDN', 'SPONDYLOEPIPHYSEAL DYSPLASIA, NISHIMURA TYPE']",0112288,618618,,,,,,,,,,
mondo:0032836,weiss-kruszka syndrome,"['WSKA', 'WEISS-KRUSZKA SYNDROME']",,618619,,,,,,,,,,
mondo:0032837,abdominal obesity-metabolic syndrome 4,"['AOMS4', 'ABDOMINAL OBESITY-METABOLIC SYNDROME 4']",0080945,618620,,,,,,,,,,
mondo:0032838,"neurodevelopmental disorder with microcephaly, arthrogryposis, and structural brain anomalies","['NEDMABA', 'NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, ARTHROGRYPOSIS, AND STRUCTURAL BRAIN ANOMALIES']",,618622,,,,,,,,,,
mondo:0032839,noonan syndrome 12,"['NS12', 'NOONAN SYNDROME 12']",0112170,618624,,,,C177120,,,,,,
mondo:0032841,"Usher syndrome, type 1M","['USHER SYNDROME, TYPE 1M', 'USH1M']",,618632,,,,,,,,,,
mondo:0032842,Siddiqi syndrome,"['SIDDIQI SYNDROME', 'SIDDIS', 'Deafness, Dystonia, Developmental Delay, and Poor Growth']",0081273,618635,,,,,,,,,,
mondo:0032843,oculopharyngeal myopathy with leukoencephalopathy 1,"['OCULOPHARYNGEAL MYOPATHY WITH LEUKOENCEPHALOPATHY 1', 'OPML1']",,618637,,,,,,,,,,
mondo:0032844,infantile liver failure syndrome 3,"['INFANTILE LIVER FAILURE SYNDROME 3', 'ILFS3']",,618641,,,,,,,,,,
mondo:0032845,spermatogenic failure 39,"['SPERMATOGENIC FAILURE 39', 'SPGF39']",0111926,618643,,,,,,,,,,
mondo:0032846,"osteogenesis imperfecta, type 20","['OI20', 'OSTEOGENESIS IMPERFECTA, TYPE XX']",0111849,618644,,,,,,,,,,
mondo:0032848,"immunodeficiency 65, susceptibility to viral infections","['IMMUNODEFICIENCY 65, SUSCEPTIBILITY TO VIRAL INFECTIONS', 'IMD65']",0111978,618648,,,,,,,,,,
mondo:0032849,"neurodevelopmental disorder with spastic quadriplegia, optic atrophy, seizures, and structural brain anomalies","['NEDSOSB', 'NEURODEVELOPMENTAL DISORDER WITH SPASTIC QUADRIPLEGIA, OPTIC ATROPHY, SEIZURES, AND STRUCTURAL BRAIN ANOMALIES', 'Halperin-Birk syndrome']",,618651,,,,,,,,,,
mondo:0032850,neurooculocardiogenitourinary syndrome,"['NOCGUS', 'NEUROOCULOCARDIOGENITOURINARY SYNDROME']",0111675,618652,,,,,,,,,,
mondo:0032851,intellectual developmental disorder with impaired language and dysmorphic facies,"['IDDILF', 'INTELLECTUAL DEVELOPMENTAL DISORDER WITH IMPAIRED LANGUAGE AND DYSMORPHIC FACIES']",,618653,,,,,,,,,,
mondo:0032852,"myopathy, congenital, with structured cores and z-line abnormalities","['Multiple Structured Core Disease', 'myopathy, congenital with structured cores and z-line abnormalities', 'MYOPATHY, CONGENITAL, WITH STRUCTURED CORES AND Z-LINE ABNORMALITIES', 'MYOCOZ']",0081342,618654,,,,,,,,,,
mondo:0032853,"myopathy, distal, 6, adult-onset, autosomal dominant","['myopathy, distal, 6, adult onset', 'MYOPATHY, DISTAL, 6, ADULT-ONSET, AUTOSOMAL DOMINANT', 'MPD6']",,618655,,,,,,,,,,
mondo:0032854,zimmermann-laband syndrome 3,"['ZLS3', 'ZIMMERMANN-LABAND SYNDROME 3']",,618658,,,,,,,,,,
mondo:0032855,neurodevelopmental disorder with dysmorphic facies and distal skeletal anomalies,"['NEDDFSA', 'NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND DISTAL SKELETAL ANOMALIES']",,618659,,,,,,,,,,
mondo:0032857,"diarrhea 11, malabsorptive, congenital","['Intractable Diarrhea of Infancy Syndrome', 'DIARRHEA 11, MALABSORPTIVE, CONGENITAL', 'DIAR11', 'Intractable Diarrhoea of Infancy Syndrome']",,618662,,,,,,,,,,
mondo:0032858,"developmental and epileptic encephalopathy, 81","['developmental and epileptic encephalopathy 81', 'EIEE81', 'DEE81', 'epileptic encephalopathy, early infantile, 81', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 81']",0112217,618663,,,,,,,,,,
mondo:0032859,spermatogenic failure 40,"['SPERMATOGENIC FAILURE 40', 'SPGF40']",0111918,618664,,,,,,,,,,
mondo:0032860,"intellectual developmental disorder, autosomal recessive 72","['MRT72', 'Mental Retardation, Autosomal Recessive 72', 'INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL RECESSIVE 72']",0080765,618665,,,,,,,,,,
mondo:0032862,"hydrocephalus, congenital communicating, 1","['HYDROCEPHALUS, CONGENITAL COMMUNICATING, 1', 'HYDCC1']",,618667,,,,,,,,,,
mondo:0032863,spermatogenic failure 41,"['SPGF41', 'SPERMATOGENIC FAILURE 41']",0111912,618670,,,,,,,,,,
mondo:0032864,"intellectual developmental disorder with speech delay, autism, and dysmorphic facies","['INTELLECTUAL DEVELOPMENTAL DISORDER WITH SPEECH DELAY, AUTISM, AND DYSMORPHIC FACIES', 'IDDSADF']",,618672,,,,,,,,,,
mondo:0032865,"pulmonary fibrosis and/or bone marrow failure, telomere-related, 5","['PFBMFT5', 'PULMONARY FIBROSIS AND/OR BONE MARROW FAILURE, TELOMERE-RELATED, 5']",,618674,,,,,,,,,,
mondo:0032866,"cortical dysplasia, complex, with other brain malformations 10","['CDCBM10', 'CORTICAL DYSPLASIA, COMPLEX, WITH OTHER BRAIN MALFORMATIONS 10']",,618677,,,,,,,,,,
mondo:0032867,"pancreatic cancer, susceptibility to, 5","['PANCREATIC CANCER, SUSCEPTIBILITY TO, 5', 'PNCA5']",,618680,,,,,,,,,,
mondo:0032868,lessel-kubisch syndrome,"['LESSEL-KUBISCH SYNDROME', 'LSKB']",,618681,,,,,,,,,,
mondo:0032869,"mitochondrial complex 5 (ATP synthase) deficiency, nuclear type 6","['MC5DN6', 'MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 6']",0111749,618683,,,,,,,,,,
mondo:0032870,intellectual developmental disorder with short stature and behavioral abnormalities,"['IDDSSBA', 'INTELLECTUAL DEVELOPMENTAL DISORDER WITH SHORT STATURE AND BEHAVIORAL ABNORMALITIES']",0111674,618687,,,,,,,,,,
mondo:0032871,"leukodystrophy, hypomyelinating, 19, transient infantile","['HLD19', 'LEUKODYSTROPHY, HYPOMYELINATING, 19, TRANSIENT INFANTILE']",0070400,618688,,,,,,,,,,
mondo:0032872,"ciliary dyskinesia, primary, 42","['Ciliary Dyskinesia, Primary, 42, Without Situs Inversus', 'CILIARY DYSKINESIA, PRIMARY, 42', 'CILD42']",0111855,618695,,,,,,,,,,
mondo:0032873,retinitis pigmentosa 87 with choroidal involvement,"['RP87', 'RETINITIS PIGMENTOSA 87 WITH CHOROIDAL INVOLVEMENT']",,618697,,,,,,,,,,
mondo:0032874,"ciliary dyskinesia, primary, 43","['CILIARY DYSKINESIA, PRIMARY, 43', 'CILD43', 'Ciliary Dyskinesia, Primary, 43, With or Without Situs Inversus']",0111856,618699,,,,,,,,,,
mondo:0032875,short stature and microcephaly with genital anomalies,"['SHORT STATURE AND MICROCEPHALY WITH GENITAL ANOMALIES', 'SSMGA']",,618702,,,,,,,,,,
mondo:0032876,neurodevelopmental disorder with absent language and variable seizures,"['NEDALVS', 'Ito-Raymond Syndrome', 'NEURODEVELOPMENTAL DISORDER WITH ABSENT LANGUAGE AND VARIABLE SEIZURES']",,618707,,,,,,,,,,
mondo:0032877,neurodevelopmental disorder with nonspecific brain abnormalities and with or without seizures,"['NEDBAS', 'NEURODEVELOPMENTAL DISORDER WITH NONSPECIFIC BRAIN ABNORMALITIES AND WITH OR WITHOUT SEIZURES']",,618709,,,,,,,,,,
mondo:0032878,"neurodevelopmental disorder with behavioral abnormalities, absent speech, and hypotonia","['NEDBASH', 'NEURODEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES, ABSENT SPEECH, AND HYPOTONIA']",,618718,,,,,,,,,,
mondo:0032879,"megabladder, congenital","['MEGABLADDER, CONGENITAL', 'MGBL']",0112014,618719,,,,,,,,,,
mondo:0032880,"developmental and epileptic encephalopathy, 82","['Got2 Deficiency', 'developmental and epileptic encephalopathy 82', 'epileptic encephalopathy, early infantile, 82', 'EIEE82', 'DEE82', 'Glutamate Oxaloacetate Transaminase, Mitochondrial, Deficiency of', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 82']",0080715,618721,,,,,,,,,,
mondo:0032881,premature ovarian failure 16,"['PREMATURE OVARIAN FAILURE 16', 'POF16']",0080873,618723,,,,,,,,,,
mondo:0032882,Heyn-Sproul-Jackson syndrome,"['HESJAS', 'Microcephaly, Short Stature, and Impaired Intellectual Development', 'HEYN-SPROUL-JACKSON SYNDROME']",,618724,,,,,,,,,,
mondo:0032883,intellectual developmental disorder with behavioral abnormalities and craniofacial dysmorphism with or without seizures,"['INTELLECTUAL DEVELOPMENTAL DISORDER WITH BEHAVIORAL ABNORMALITIES AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT SEIZURES', 'IDDBCS']",,618725,,,,,,,,,,
mondo:0032884,"ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies","['ectodermal dysplasia with facial dysmorphism and acral, ocular, and brain anomalies, somatic mosaic', 'ECTODERMAL DYSPLASIA WITH FACIAL DYSMORPHISM AND ACRAL, OCULAR, AND BRAIN ANOMALIES', 'EDFAOB']",,618727,,,,,,,,,,
mondo:0032885,"spondyloepimetaphyseal dysplasia, Isidor-Toutain type","['SPONDYLOEPIMETAPHYSEAL DYSPLASIA, ISIDOR-TOUTAIN TYPE', 'SEMDIST']",,618728,,,,,,,,,,
mondo:0032886,Liang-Wang syndrome,"['LIWAS', 'LIANG-WANG SYNDROME']",,618729,,,,,,,,,,
mondo:0032887,"neurodevelopmental disorder with microcephaly, cortical malformations, and spasticity","['Vandervore-Schot Syndrome', 'NEDMCMS', 'NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, CORTICAL MALFORMATIONS, AND SPASTICITY']",,618730,,,,,,,,,,
mondo:0032888,neurodevelopmental disorder with brain anomalies and with or without vertebral or cardiac anomalies,"['NEURODEVELOPMENTAL DISORDER WITH BRAIN ANOMALIES AND WITH OR WITHOUT VERTEBRAL OR CARDIAC ANOMALIES', 'NEDBAVC']",,618731,,,,,,,,,,
mondo:0032889,Poirier-Bienvenu neurodevelopmental syndrome,"['POIRIER-BIENVENU NEURODEVELOPMENTAL SYNDROME', 'POBINDS']",,618732,,,,,,,,,,
mondo:0032890,neuromuscular disease and ocular or auditory anomalies with or without seizures,"['NEUROMUSCULAR DISEASE AND OCULAR OR AUDITORY ANOMALIES WITH OR WITHOUT SEIZURES', 'NMOAS']",,618733,,,,,,,,,,
mondo:0032891,"aneurysm, intracranial berry, 12","['ANEURYSM, INTRACRANIAL BERRY, 12', 'ANIB12']",0080975,618734,,,,,,,,,,
mondo:0032892,structural brain anomalies with impaired intellectual development and craniosynostosis,"['BAIDCS', 'STRUCTURAL BRAIN ANOMALIES WITH IMPAIRED INTELLECTUAL DEVELOPMENT AND CRANIOSYNOSTOSIS']",,618736,,,,,,,,,,
mondo:0032893,"pachygyria, microcephaly, developmental delay, and dysmorphic facies, with or without seizures","['PAMDDFS', 'PACHYGYRIA, MICROCEPHALY, DEVELOPMENTAL DELAY, AND DYSMORPHIC FACIES, WITH OR WITHOUT SEIZURES']",0081266,618737,,,,,,,,,,
mondo:0032894,"neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy","['NEURODEVELOPMENTAL DISORDER WITH EPILEPSY, SPASTICITY, AND BRAIN ATROPHY', 'NEDESBA']",,618741,,,,,,,,,,
mondo:0032895,"developmental and epileptic encephalopathy, 83","['epileptic encephalopathy, early infantile, 83', 'EIEE83', 'developmental and epileptic encephalopathy 83', 'DEE83', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 83', 'Barakat-Perenthaler Syndrome']",0112218,618744,,,,,,,,,,
mondo:0032896,spermatogenic failure 42,"['SPERMATOGENIC FAILURE 42', 'SPGF42']",0111923,618745,,,,,,,,,,
mondo:0032897,intellectual developmental disorder with hypotonia and behavioral abnormalities,"['INTELLECTUAL DEVELOPMENTAL DISORDER WITH HYPOTONIA AND BEHAVIORAL ABNORMALITIES', 'IDDHBA']",,618748,,,,,,,,,,
mondo:0032898,spermatogenic failure 43,"['SPERMATOGENIC FAILURE 43', 'SPGF43']",0111917,618751,,,,,,,,,,
mondo:0032899,"neutropenia, severe congenital, 8, autosomal dominant","['SCN8', 'Shwachman-Diamond Syndrome-Like', 'Neutropenia, Severe Congenital, 8, Autosomal Dominant, With or Without Pancreatic Dysfunction And/Or Neurologic Abnormalities', 'NEUTROPENIA, SEVERE CONGENITAL, 8, AUTOSOMAL DOMINANT']",0112135,618752,,,,,,,,,,
mondo:0032900,neurodevelopmental disorder with hypotonia and autistic features with or without hyperkinetic movements,"['NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND AUTISTIC FEATURES WITH OR WITHOUT HYPERKINETIC MOVEMENTS', 'NEDHAHM']",,618760,,,,,,,,,,
mondo:0032901,Catifa syndrome,"['CATIFA', 'Cleft Lip, Cataract, Tooth Abnormality, Impaired Intellectual Development, Facial Dysmorphism, and Attention-Deficit Hyperactivity Disorder', 'CATIFA SYNDROME']",,618761,,,,,,,,,,
mondo:0032902,Joubert syndrome 36,"['JBTS36', 'JOUBERT SYNDROME 36']",,618763,,,,,,,,,,
mondo:0032903,"arthrogryposis multiplex congenita 4, neurogenic, with agenesis of the corpus callosum","['AMCNACC', 'Zain Syndrome', 'arthrogryposis multiplex congenita, neurogenic, with agenesis of the corpus callosum']",0080980,618766,,,,,,,,,,
mondo:0032904,"corneal dystrophy, Meesmann, 2","['CORNEAL DYSTROPHY, MEESMANN, 2', 'MECD2', 'meesmann corneal dystrophy 2']",0080671,618767,,,,,,,,,,
mondo:0032905,"spastic paraplegia 81, autosomal recessive","['SPG81', 'SPASTIC PARAPLEGIA 81, AUTOSOMAL RECESSIVE']",,618768,,,,,,,,,,
mondo:0032906,"spastic paraplegia 82, autosomal recessive","['SPASTIC PARAPLEGIA 82, AUTOSOMAL RECESSIVE', 'SPG82']",0112343,618770,,,,,,,,,,
mondo:0032907,lymphatic malformation 8,"['LMPHM8', 'LYMPHATIC MALFORMATION 8']",,618773,,,,,,,,,,
mondo:0032908,CEBALID syndrome,"['MCTT', 'MN1 C-terminal truncation syndrome', 'Craniofacial Defects, Dysmorphic Ears, Structural Brain Abnormalities, Expressive Language Delay, and Impaired Intellectual Development', 'CEBALID SYNDROME', 'CEBALID']",,618774,,,,,,,,,,
mondo:0032909,"mitochondrial complex 3 deficiency, nuclear type 10","['MITOCHONDRIAL COMPLEX III DEFICIENCY, NUCLEAR TYPE 10', 'MC3DN10']",,618775,,,,,,,,,,
mondo:0032910,"mitochondrial complex 1 deficiency, nuclear type 34","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 34', 'MC1DN34']",0112091,618776,,,,,,,,,,
mondo:0032911,"hearing loss, autosomal dominant 75","['DEAFNESS, AUTOSOMAL DOMINANT 75', 'deafness, autosomal dominant 75', 'DFNA75']",0112166,618778,,,,,,,,,,
mondo:0032912,Coffin-Siris syndrome 11,"['CSS11', 'COFFIN-SIRIS SYNDROME 11']",0112372,618779,,,,,,,,,,
mondo:0032913,"congenital heart defects, multiple types, 7","['CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 7', 'CHTD7']",,618780,,,,,,,,,,
mondo:0032914,"ciliary dyskinesia, primary, 44","['CILD44', 'Ciliary Dyskinesia, Primary, 44, Without Situs Inversus', 'CILIARY DYSKINESIA, PRIMARY, 44']",0111851,618781,,,,,,,,,,
mondo:0032915,long QT syndrome 16,"['LQT16', 'Ventricular Tachycardia, Catecholaminergic Polymorphic 6', 'long QT syndrome 16']",,618782,,,,,,,,,,
mondo:0032916,Imagawa-Matsumoto syndrome,"['IMAGAWA-MATSUMOTO SYNDROME', 'IMMAS']",,618786,,,,,,,,,,
mondo:0032917,"hearing loss, autosomal dominant 76","['deafness, autosomal dominant 76', 'DFNA76', 'DEAFNESS, AUTOSOMAL DOMINANT 76']",0112167,618787,,,,,,,,,,
mondo:0032918,"developmental and epileptic encephalopathy, 84","['developmental and epileptic encephalopathy 84', 'DEE84', 'EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 84', 'EIEE84', 'Jamuar Syndrome', 'epileptic encephalopathy, early infantile, 84']",0112219,618792,,,,,,,,,,
mondo:0032919,intellectual developmental disorder 62,"['INTELLECTUAL DEVELOPMENTAL DISORDER 62', 'MRD62', 'Mental Retardation, Autosomal Dominant 62']",,618793,,,,,,,,,,
mondo:0032920,juvenile arthritis due to defect in LACC1,"['JUVAR', 'JUVENILE ARTHRITIS']",,618795,,,,,,,,,,
mondo:0032921,"neurodevelopmental disorder with hypotonia, neonatal respiratory insufficiency, and thermodysregulation","['NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA, NEONATAL RESPIRATORY INSUFFICIENCY, AND THERMODYSREGULATION', 'NEDHRIT']",,618797,,,,,,,,,,
mondo:0032922,Beck-Fahrner syndrome,"['BEFAHRS', 'BECK-FAHRNER SYNDROME']",,618798,,,,,,,,,,
mondo:0032923,"spinocerebellar ataxia, autosomal recessive 28","['SCAR28', 'SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 28']",0070409,618800,,,,,,,,,,
mondo:0032924,"ciliary dyskinesia, primary, 45","['Ciliary Dyskinesia, Primary, 45, Without Situs Inversus', 'CILD45', 'CILIARY DYSKINESIA, PRIMARY, 45']",0111857,618801,,,,,,,,,,
mondo:0032925,"respiratory papillomatosis, juvenile recurrent, congenital","['RESPIRATORY PAPILLOMATOSIS, JUVENILE RECURRENT, CONGENITAL', 'JRRP']",,618803,,,,,,,,,,
mondo:0032926,sandestig-stefanova syndrome,"['SANDSTEF', 'SANDESTIG-STEFANOVA SYNDROME']",0081272,618804,,,,,,,,,,
mondo:0032927,triokinase and FMN cyclase deficiency syndrome,"['TKFCD', 'TRIOKINASE AND FMN CYCLASE DEFICIENCY SYNDROME']",,618805,,,,,,,,,,
mondo:0032928,"T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant","['T-CELL LYMPHOPENIA, INFANTILE, WITH OR WITHOUT NAIL DYSTROPHY, AUTOSOMAL DOMINANT', 'TLIND']",,618806,,,,,,,,,,
mondo:0032930,intellectual developmental disorder with poor growth and with or without seizures or ataxia,"['INTELLECTUAL DEVELOPMENTAL DISORDER WITH POOR GROWTH AND WITH OR WITHOUT SEIZURES OR ATAXIA', 'IDPOGSA']",,618808,,,,,,,,,,
mondo:0032931,"pontocerebellar hypoplasia, hypotonia, and respiratory insufficiency syndrome, neonatal lethal","['Chromosome 1P36.33 Deletion Syndrome, Atad3 Gene Cluster, Autosomal Recessive', 'PHRINL', 'PONTOCEREBELLAR HYPOPLASIA, HYPOTONIA, AND RESPIRATORY INSUFFICIENCY SYNDROME, NEONATAL LETHAL', 'fatal pontocerebellar hypoplasia-hypotonia-respiratory distress syndrome', 'fatal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome', 'Phrinl Syndrome']",,618810,615954,,,,,,,,,
mondo:0032932,mitochondrial DNA depletion syndrome 18,"['MITOCHONDRIAL DNA DEPLETION SYNDROME 18', 'MTDPS18']",,618811,,,,,,,,,,
mondo:0032933,"chromosome 1p36.33 duplication syndrome, atad3 gene cluster, autosomal dominant","['CHROMOSOME 1p36.33 DUPLICATION SYNDROME, ATAD3 GENE CLUSTER, AUTOSOMAL DOMINANT']",,618815,,,,,,,,,,
mondo:0032934,genitourinary and/or brain malformation syndrome,"['genitourinary and/or/brain malformation syndrome', 'GUBS', 'GENITOURINARY AND/OR BRAIN MALFORMATION SYNDROME']",,618820,,,,,,,,,,
mondo:0032935,rhizomelic limb shortening with dysmorphic features,"['RLSDF', 'RHIZOMELIC LIMB SHORTENING WITH DYSMORPHIC FEATURES']",,618821,,,,,,,,,,
mondo:0032936,"myopathy, congenital, with respiratory insufficiency and bone fractures","['MYORIBF', 'MYOPATHY, CONGENITAL, WITH RESPIRATORY INSUFFICIENCY AND BONE FRACTURES']",0081343,618822,,,,,,,,,,
mondo:0032937,"myopathy, congenital proximal, with minicore lesions","['MYOPMIL', 'MYOPATHY, CONGENITAL PROXIMAL, WITH MINICORE LESIONS']",0081344,618823,,,,,,,,,,
mondo:0032938,"basal ganglia calcification, idiopathic, 8, autosomal recessive","['IBGC8', 'BASAL GANGLIA CALCIFICATION, IDIOPATHIC, 8, AUTOSOMAL RECESSIVE']",,618824,,,,,,,,,,
mondo:0032939,"intellectual developmental disorder, autosomal dominant 63, with macrocephaly","['INTELLECTUAL DEVELOPMENTAL DISORDER, AUTOSOMAL DOMINANT 63, WITH MACROCEPHALY', 'Mental Retardation, Autosomal Dominant 63, With Macrocephaly', 'MRD63']",,618825,,,,,,,,,,
mondo:0032940,retinitis pigmentosa 88,"['RETINITIS PIGMENTOSA 88', 'RP88']",0112145,618826,,,,,,,,,,
mondo:0032941,myopia 27,"['MYP27', 'MYOPIA 27']",,618827,,,,,,,,,,
mondo:0032942,neurodevelopmental disorder with microcephaly and dysmorphic facies,"['NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY AND DYSMORPHIC FACIES', 'nabais sa-de vries syndrome, type 1', 'NEDMIDF']",,618828,,,,,,,,,,
mondo:0032943,neurodevelopmental disorder with relative macrocephaly and with or without cardiac or endocrine anomalies,"['NEDMACE', 'NEURODEVELOPMENTAL DISORDER WITH RELATIVE MACROCEPHALY AND WITH OR WITHOUT CARDIAC OR ENDOCRINE ANOMALIES', 'nabais sa-de vries syndrome, type 2']",,618829,,,,,,,,,,
mondo:0033004,polycystic kidney disease 4,"['polycystic kidney disease 4 with or without hepatic disease', 'polycystic kidney disease 4 with or without polycystic liver disease', 'polycystic kidney disease, infantile, type 1', 'PKD3', 'hepatic fibrosis, congenital', 'polycystic kidney disease 4, with or without hepatic disease', 'PKD4', 'PKD3, formerly', 'polycystic kidney disease 4', 'polycystic kidney disease, autosomal recessive', 'polycystic kidney and hepatic disease 1']",0080212,263200,731,C0085548,,,,,,,,
mondo:0033005,Galloway-Mowat syndrome 1,"['nephrosis-microcephaly syndrome', 'nephrosis-neuronal dysmigration syndrome', 'Galloway syndrome', 'cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities', 'GAMOS1', 'cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities', 'Galloway-Mowat syndrome 1', 'spinocerebellar ataxia, autosomal recessive 5, formerly', 'microcephaly, hiatal hernia, and nephrotic syndrome', 'spinocerebellar ataxia, autosomal recessive 5']",0060364,251300,,CN031715,,,,,,,,
mondo:0033006,"Galloway-Mowat syndrome 2, X-linked","['Galloway-Mowat syndrome 2', 'GAMOS2', 'Galloway-Mowat syndrome 2, X-linked, X-linked recessive', 'Galloway-Mowat syndrome 2, X-linked']",0080244,301006,,CN570502,"['-0.0202', '0.04718', '0.01633', '-0.01787', '0.01068', '-0.06854', '-0.0008717', '0.06223', '-0.0441', '-0.04318', '-0.012886', '0.00213', '0.007076', '0.009224', '-0.00827', '-0.02797', '-0.003195', '-0.02', '-0.0125', '-0.0974', '-0.01949', '-0.00904', '0.06476', '-0.02232', '0.02193', '-0.005116', '-0.02121', '-0.0228', '0.003471', '-0.04205', '0.05832', '-0.006798', '0.0705', '0.0227', '0.00989', '-0.03403', '-0.0184', '-0.0333', '-0.00952', '-0.06168', '0.01544', '-0.04626', '0.014114', '-0.01371', '-0.01242', '-0.04135', '-0.02701', '0.01631', '0.002106', '0.0177', '-0.002857', '-0.01464', '0.003004', '-0.008766', '-0.02739', '-0.0168', '0.05145', '-0.01723', '-0.0692', '0.0153', '0.03114', '0.03412', '0.00609', '0.01129', '0.00608', '0.01671', '0.0632', '0.0428', '-0.0475', '0.06052', '-0.03766', '0.00593', '0.001773', '-0.04004', '0.02623', '0.03674', '-0.000627', '0.002348', '-0.03482', '-0.02646', '0.01846', '-0.01073', '-0.00739', '0.04352', '-0.00351', '0.016', '0.01878', '0.06125', '0.06256', '-0.001557', '0.02269', '0.06006', '0.0171', '0.00179', '0.10333', '0.02168', '0.0379', '-0.06915', '-0.0002406', '0.006535']",,,,,,,
mondo:0033007,Galloway-Mowat syndrome 3,"['GAMOS3', 'Galloway-Mowat syndrome 3']",0080245,617729,,CN570505,,,,,,,,
mondo:0033008,Galloway-Mowat syndrome 4,"['Galloway-Mowat syndrome 4', 'GAMOS4']",0080246,617730,,CN570506,,,,,,,,
mondo:0033009,Galloway-Mowat syndrome 5,"['GAMOS5', 'Galloway-Mowat syndrome 5']",0080247,617731,,CN570507,,,,,,,,
mondo:0033010,erythrokeratodermia variabilis et progressiva 1,"['Greither disease', 'erythrokeratodermia Figurata, congenital familial, in plaques', 'erythrokeratodermia variabilis ET progressiva 1', 'EKVP1', 'erythrokeratodermia variabilis with erythema Gyratum Repens', 'erythrokeratodermia variabilis Et progressiva', 'erythrokeratodermia, progressive symmetric', 'keratosis palmoplantaris transgrediens Et progrediens', 'erythrokeratodermia variabilis']",0111195,133200,495,,"['-0.09656', '0.1351', '-0.02724', '-0.1108', '0.1097', '-0.3533', '-0.07764', '-0.03665', '-0.03122', '-0.1418', '-0.01694', '-0.0714', '-0.09595', '-0.1624', '-0.0202', '0.1443', '0.1727', '-0.201', '-0.00797', '-0.4202', '-0.0928', '0.006714', '0.1951', '-0.0626', '0.1081', '0.0813', '-0.057', '-0.0252', '-0.1383', '-0.3745', '0.1384', '-0.0771', '0.09045', '0.1276', '0.1285', '-0.1221', '-0.0491', '-0.1233', '-0.02226', '-0.1925', '0.05447', '-0.3228', '0.1263', '-0.1165', '0.01157', '-0.2408', '-0.2352', '0.16', '0.09375', '-0.1256', '-0.1543', '-0.0854', '0.05746', '0.129', '-0.0785', '-0.07666', '0.443', '-0.00388', '-0.367', '0.0404', '0.08276', '0.05112', '-0.08215', '-0.0474', '0.1173', '0.02884', '0.2064', '0.25', '-0.06366', '0.4592', '-0.309', '-0.1493', '0.07495', '0.1547', '0.1005', '0.1545', '0.04086', '0.06052', '-0.02397', '0.01695', '0.1037', '0.1974', '-0.03348', '0.0866', '-0.05292', '0.10925', '0.10345', '0.4038', '0.1259', '0.08875', '0.1942', '0.1721', '-0.06573', '0.0619', '0.4277', '0.085', '0.2932', '-0.2764', '-0.05313', '0.04572']",,,,,,,
mondo:0033012,erythrokeratodermia variabilis et progressiva 2,"['EKVP2', 'erythrokeratodermia variabilis ET progressiva 2']",0080248,617524,,C4479618,,,,,,,,
mondo:0033013,erythrokeratodermia variabilis et progressiva 3,"['erythrokeratodermia variabilis ET progressiva 3', 'EKVP3']",0080249,617525,,C4479619,,,,,,,,
mondo:0033014,erythrokeratodermia variabilis et progressiva 4,"['erythrokeratodermia variabilis ET progressiva 4', 'EKVP4']",0080250,617526,,C4479620,,,,,,,,
mondo:0033015,erythrokeratodermia variabilis et progressiva 5,"['EKVP5', 'erythrokeratodermia variabilis ET progressiva 5']",0080251,617756,,,,,,,,,,
mondo:0033043,"spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy","['SPAX8', 'spastic ataxia 8, autosomal recessive, with hypomyelinating leukodystrophy', 'spastic ataxia 8']",0080252,617560,527497,C4479653,"['-0.03912', '0.1777', '0.003616', '-0.05203', '0.01467', '-0.1908', '-0.05676', '0.1279', '-0.1488', '-0.0167', '-0.10645', '-0.00984', '-0.03482', '-0.0787', '0.1635', '-0.1317', '0.02028', '-0.11566', '-0.02039', '-0.2079', '-0.0463', '-0.07947', '-0.0217', '-0.07587', '0.04584', '-0.0328', '-0.03384', '-0.0515', '0.01093', '-0.1171', '0.0492', '0.0248', '0.1572', '0.01275', '-0.01886', '-0.0759', '-0.0223', '-0.1087', '-0.0751', '-0.0957', '0.02391', '-0.1993', '0.0346', '0.015236', '-0.04144', '-0.2102', '-0.05826', '0.1138', '0.00337', '-0.04657', '0.01942', '0.04044', '-0.09814', '-0.011345', '-0.002426', '-0.05804', '0.2089', '-0.0333', '-0.1868', '0.0365', '0.077', '0.07733', '0.10944', '0.10046', '-0.0728', '-0.00832', '0.15', '0.0862', '-0.08154', '0.1558', '-0.1219', '0.0468', '0.04584', '-0.1609', '0.10516', '0.07184', '0.010315', '-0.02336', '-0.05093', '-0.0602', '-0.01021', '-0.03146', '-0.01941', '0.1769', '0.002527', '0.02878', '0.00331', '0.1289', '0.0946', '0.06015', '0.0696', '0.1531', '0.0442', '0.03726', '0.334', '0.10095', '0.1366', '-0.1376', '0.01608', '0.03946']",,,,,,,
mondo:0033044,Meckel syndrome 13,"['Meckel syndrome, type 13', 'MKS13', 'Meckel syndrome 13']",0080253,617562,,,,,,,,,,
mondo:0033045,orofaciodigital syndrome 16,"['orofaciodigital syndrome XVI', 'OFD16', 'Ofds 16', 'oral-Facial-digital syndrome, type 16']",0080254,617563,,CN317535,,,,,,,,
mondo:0033046,Meier-Gorlin syndrome 8,"['Meier-Gorlin syndrome 8', 'MGORS8']",0080255,617564,,C4479655,,,,,,,,
mondo:0033047,Perrault syndrome 6,"['PRLTS6', 'Perrault syndrome 6']",0080256,617565,,C4479656,,,,,,,,
mondo:0033091,"ichthyosis, congenital, autosomal recessive 14","['autosomal recessive congenital ichthyosis 14', 'ARCI14', 'ichthyosis, congenital, autosomal recessive 14']",0080258,617571,313,CN317536,,,,,,,,
mondo:0033092,"ichthyosis, congenital, autosomal recessive 13","['ARCI13', 'ichthyosis, congenital, autosomal recessive 13', 'autosomal recessive congenital ichthyosis 13']",0080257,617574,,CN321864,,,,,,,,
mondo:0033115,"spinocerebellar ataxia, autosomal recessive 25","['spinocerebellar ataxia, autosomal recessive 25', 'autosomal recessive spinocerebellar ataxia 25', 'SCAR25']",0080259,617584,,CN349871,,,,,,,,
mondo:0033116,"spinocerebellar ataxia, autosomal recessive 26","['SCAR26', 'autosomal recessive spinocerebellar ataxia 26', 'spinocerebellar ataxia, autosomal recessive 26']",0080260,617633,,CN417133,,,,,,,,
mondo:0033123,exudative vitreoretinopathy 7,"['EVR7', 'exudative vitreoretinopathy 7']",0080264,617572,,CN321863,,,,,,,,
mondo:0033135,"Charcot-Marie-Tooth disease, demyelinating, type 1G","['Charcot-Marie-Tooth disease, demyelinating, type 1G', 'CMT1G']",0111560,618279,476394,,,,,,,,,
mondo:0033169,curariform drugs toxicity,,,,413693,,,,,,,,,
mondo:0033170,statin toxicity,,,,413696,,,,,,,,,
mondo:0033181,phenytoin or carbamazepine toxicity,,,,414750,,,,,,,,,
mondo:0033198,"hearing loss, autosomal recessive 106","['deafness autosomal recessive 106', 'DFNB106', 'autosomal recessive nonsyndromic deafness 106', 'deafness, autosomal recessive 106']",0080261,617637,,,,,,,,,,
mondo:0033199,"hearing loss, autosomal recessive 107","['deafness, autosomal recessive 107', 'autosomal recessive nonsyndromic deafness 107', 'DFNB107']",0080262,617639,,,,,,,,,,
mondo:0033200,"hearing loss, autosomal recessive 108","['DFNB108', 'autosomal recessive nonsyndromic deafness 108', 'deafness, autosomal recessive 108']",0080263,617654,,,,,,,,,,
mondo:0033201,"hearing loss, autosomal recessive 57","['DFNB57', 'deafness, autosomal recessive 57']",0111635,618003,,CN248511,"['-0.01013', '0.11865', '0.02463', '-0.0601', '0.04593', '-0.1448', '0.004795', '0.128', '-0.07855', '-0.08453', '-0.03506', '-0.03455', '-0.007595', '0.00734', '-0.0202', '-0.04785', '0.01339', '-0.06223', '-0.02942', '-0.2057', '-0.0682', '-0.05835', '0.04242', '-0.03433', '0.0388', '0.002928', '-0.01665', '-0.05795', '0.03638', '-0.08716', '0.0736', '0.03265', '0.11536', '0.0443', '-0.00889', '-0.0639', '-0.01837', '-0.0663', '-0.001682', '-0.1193', '0.0209', '-0.112', '0.05743', '-0.03986', '-0.01257', '-0.135', '-0.05228', '0.0715', '0.03354', '0.0682', '0.008644', '-0.03075', '0.017', '-0.02773', '-0.04486', '-0.08527', '0.1245', '-0.00792', '-0.1526', '0.03818', '0.08105', '0.0448', '0.0266', '0.02644', '-0.02214', '0.012596', '0.1138', '0.09625', '-0.1148', '0.1338', '-0.10315', '-0.01343', '0.03983', '-0.1224', '0.1166', '0.0577', '0.013885', '-0.0182', '-0.06107', '-0.03223', '-0.001733', '-0.02907', '0.03378', '0.1158', '-0.00705', '0.02692', '0.04034', '0.095', '0.0911', '0.0794', '0.0801', '0.11743', '-0.01137', '0.01569', '0.2466', '0.08075', '0.11725', '-0.161', '-0.01688', '0.0412']",,,,,,,
mondo:0033202,"hearing loss, autosomal recessive 109","['DFNB109', 'deafness, autosomal recessive 109']",0111639,618013,,CN248519,,,,,,,,
mondo:0033203,nephrotic syndrome 14,"['primary adrenal insufficiency-steroid-resistant nephrotic syndrome due to SGPL1 deficiency', 'nephrotic syndrome 14', 'nephrotic syndrome, type 14', 'NPHS14', 'familial steroid-resistant nephrotic syndrome with adrenal insufficiency']",0080265,617575,506334,CN339707,,,,,,,,
mondo:0033204,"ciliary dyskinesia, primary, 37","['ciliary dyskinesia, primary, 37, with or without situs inversus', 'CILD37', 'ciliary dyskinesia, primary, 37', 'primary ciliary dyskinesia 37']",0080266,617577,,,,,,,,,,
mondo:0033258,"hearing loss, autosomal dominant 71","['DFNA71', 'deafness, autosomal dominant 71', 'autosomal dominant nonsyndromic deafness 71']",0080267,617605,,,,,,,,,,
mondo:0033259,"hearing loss, autosomal dominant 72","['deafness, autosomal dominant 72', 'autosomal dominant nonsyndromic deafness 72', 'DFNA72']",0080268,617606,,,,,,,,,,
mondo:0033260,"hearing loss, autosomal dominant 73","['DFNA73', 'deafness, autosomal dominant 73', 'autosomal dominant nonsyndromic deafness 73']",0080269,617663,,CN461628,,,,,,,,
mondo:0033261,"hearing loss, autosomal dominant 34, with or without inflammation","['deafness, autosomal dominant 34, with or without inflammation', 'autosomal dominant nonsyndromic deafness 34', 'DFNA34']",0080270,617772,,CN653906,,,,,,,,
mondo:0033262,nephrotic syndrome 15,"['NPHS15', 'nephrotic syndrome, type 15', 'nephrotic syndrome 15']",0080271,617609,,CN388854,,,,,,,,
mondo:0033280,nephrotic syndrome 16,"['nephrotic syndrome 16', 'NPHS16', 'nephrotic syndrome, type 16']",0080272,617783,,CN651336,,,,,,,,
mondo:0033281,polycystic kidney disease 5,"['polycystic kidney disease 5', 'DZIP1L polycystic kidney disease', 'PKD5']",0080273,617610,731,,,,,,,,,
mondo:0033282,multiple mitochondrial dysfunctions syndrome 5,"['multiple mitochondrial dysfunctions syndrome 5', 'MMDS5']",0080274,617613,569274,CN388855,,,,,,,,
mondo:0033304,"nonsyndromic deafness, Y-linked",,0111757,,,,,,,,,,,
mondo:0033308,Joubert syndrome 30,"['JBTS30', 'Joubert syndrome 30']",0080275,617622,,,,,,,,,,
mondo:0033309,Joubert syndrome 32,"['JBTS32', 'Joubert syndrome 32']",0080278,617757,,CN596207,,,,,,,,
mondo:0033310,Joubert syndrome 31,"['JBTS31', 'Joubert syndrome 31']",0080277,617761,,,,,,,,,,
mondo:0033311,Joubert syndrome 33,"['Joubert syndrome 33', 'JBTS33']",0080279,617767,,CN601375,,,,,,,,
mondo:0033312,schizophrenia 19,"['schizophrenia 19', 'schizophrenia 19, susceptibility to', 'SCZD19', 'schizophrenia 19 with or without an affective disorder']",0080281,617629,,CN404275,,,,,,,,
mondo:0033352,"neuropathy, congenital hypomelinating",['CHN'],,,,,,,,,,,,
mondo:0033361,"developmental and epileptic encephalopathy, 52","['epileptic encephalopathy, early infantile, 52', 'EIEE52', 'DEE52', 'developmental and epileptic encephalopathy 52']",0080455,617350,,C4479236,,,,,,,,
mondo:0033362,"developmental and epileptic encephalopathy, 53","['epileptic encephalopathy, early infantile, 53', 'developmental and epileptic encephalopathy 53', 'EIEE53', 'DEE53']",0080464,617389,,C4479313,,,,,,,,
mondo:0033363,"developmental and epileptic encephalopathy, 54","['DEE54', 'EIEE54', 'developmental and epileptic encephalopathy 54', 'epileptic encephalopathy, early infantile, 54']",0080418,617391,,C4479319,,,,,,,,
mondo:0033364,"developmental and epileptic encephalopathy, 55","['glycosylphosphatidylinositol biosynthesis defect 14', 'developmental and epileptic encephalopathy 55', 'epileptic encephalopathy, early infantile, 55', 'infantile epileptic encephalopathy 55', 'DEE55', 'EIEE55']",0080283,617599,,,,,,,,,,
mondo:0033365,"developmental and epileptic encephalopathy, 56","['developmental and epileptic encephalopathy 56', 'infantile epileptic encephalopathy 56', 'DEE56', 'EIEE56', 'epileptic encephalopathy, early infantile, 56']",0080282,617665,,CN477042,,,,,,,,
mondo:0033366,"developmental and epileptic encephalopathy, 57","['infantile epileptic encephalopathy 57', 'developmental and epileptic encephalopathy 57', 'EIEE57', 'DEE57', 'epileptic encephalopathy, early infantile, 57']",0080284,617771,,CN633295,,,,,,,,
mondo:0033367,"developmental and epileptic encephalopathy, 58","['EIEE58', 'epileptic encephalopathy, early infantile, 58', 'developmental and epileptic encephalopathy 58', 'DEE58', 'infantile epileptic encephalopathy 58']",0080285,617830,442835,CN757795,,,,,,,,
mondo:0033368,"developmental and epileptic encephalopathy, 59","['epileptic encephalopathy, early infantile, 59', 'EIEE59', 'developmental and epileptic encephalopathy 59', 'infantile epileptic encephalopathy 59', 'DEE59']",0080291,617904,,CN870853,,,,,,,,
mondo:0033369,"developmental and epileptic encephalopathy, 60","['epileptic encephalopathy, early infantile, 60', 'DEE60', 'EIEE60', 'developmental and epileptic encephalopathy 60']",0080432,617929,,CN244549,,,,,,,,
mondo:0033370,"developmental and epileptic encephalopathy, 61","['DEE61', 'epileptic encephalopathy, early infantile, 61', 'developmental and epileptic encephalopathy 61', 'EIEE61']",0080434,617933,,CN244550,,,,,,,,
mondo:0033371,"developmental and epileptic encephalopathy, 62","['epileptic encephalopathy, early infantile, 62', 'EIEE62', 'DEE62', 'developmental and epileptic encephalopathy 62']",0080420,617938,,CN244551,,,,,,,,
mondo:0033372,"developmental and epileptic encephalopathy, 63","['EIEE63', 'developmental and epileptic encephalopathy 63', 'DEE63', 'epileptic encephalopathy, early infantile, 63']",0080426,617976,,CN244926,,,,,,,,
mondo:0033373,"developmental and epileptic encephalopathy, 64","['EIEE64', 'DEE64', 'epileptic encephalopathy, early infantile, 64', 'developmental and epileptic encephalopathy 64']",0070375,618004,,CN248512,,,,,,,,
mondo:0033374,"developmental and epileptic encephalopathy, 65","['DEE65', 'developmental and epileptic encephalopathy 65', 'epileptic encephalopathy, early infantile, 65', 'EIEE65']",0080430,618008,,CN248516,"['-0.01573', '0.01348', '-0.0009475', '0.00353', '0.01073', '-0.02902', '0.001466', '0.03049', '-0.01964', '-0.004223', '-0.01575', '-0.000718', '0.00082', '0.002136', '0.000267', '-0.02182', '-0.013214', '-0.012276', '-0.01924', '-0.0405', '-0.005474', '0.001116', '0.02347', '-0.0124', '0.01646', '-0.01381', '0.006042', '-0.00687', '-0.00403', '-0.01003', '0.01186', '-0.00141', '0.0329', '0.002174', '0.0002346', '-0.001136', '-0.000932', '-0.006042', '-0.0176', '-0.00705', '0.003332', '-0.01816', '0.01543', '-0.0042', '0.00713', '-0.01468', '-0.01445', '0.01178', '0.003456', '0.01822', '0.004818', '0.01015', '0.008575', '0.00688', '-0.008354', '-0.0098', '0.01949', '-0.01278', '-0.02737', '0.001326', '0.013794', '0.003643', '0.00586', '-0.004173', '0.00526', '0.001868', '0.02219', '0.02177', '-0.01746', '0.0169', '-0.012596', '0.00619', '-0.003569', '-0.02324', '0.01802', '0.01758', '0.01', '0.001329', '-0.01712', '-0.00856', '-0.006912', '-0.001827', '-0.01744', '0.004547', '0.000345', '0.01161', '0.00968', '0.006283', '0.03632', '0.0099', '0.00834', '0.02719', '-0.003096', '0.01197', '0.03085', '0.02036', '0.02731', '-0.01712', '0.001152', '0.001818']",,,,,,,
mondo:0033375,orofaciodigital syndrome 17,"['oral-Facial-digital syndrome, type 17', 'OFD17', 'orofaciodigital syndrome XVII', 'Ofds 17']",0080289,617926,,CN902091,,,,,,,,
mondo:0033479,spinocerebellar ataxia 44,"['SCA44', 'spinocerebellar ataxia 44']",0080286,617691,631095,CN492437,,,,,,,,
mondo:0033480,spinocerebellar ataxia 45,"['SCA45', 'spinocerebellar ataxia 45']",0080287,617769,589527,CN623017,,,,,,,,
mondo:0033481,spinocerebellar ataxia 46,"['SCA46', 'spinocerebellar ataxia 46', 'spinocerebellar ataxia, 46, autosomal dominant, with sensory axonal neuropathy']",0080288,617770,589522,CN623018,,,,,,,,
mondo:0033482,spinocerebellar ataxia 47,"['SCA47', 'spinocerebellar ataxia 47', 'PUM1-related cerebellar ataxia']",0111743,617931,642747,CN244564,"['-0.003756', '0.00632', '-0.015045', '0.001125', '0.004562', '-0.02914', '0.00379', '0.01848', '-0.02003', '-0.01573', '-0.010475', '-0.006996', '-0.01041', '-0.00638', '0.0114', '-0.009346', '-0.01013', '-0.01051', '0.001771', '-0.03674', '-0.0078', '-0.01811', '-0.014465', '-0.008865', '0.01497', '-0.006226', '0.004005', '-0.00643', '-0.010315', '-0.0105', '-0.004868', '0.004997', '0.024', '0.00535', '0.0001552', '-0.000392', '-0.0003152', '-0.014015', '-0.0111', '-0.0106', '0.01133', '-0.02211', '0.00885', '-0.00586', '0.003952', '-0.02742', '-0.01143', '0.008194', '-0.00243', '0.005283', '-0.001005', '-0.004425', '-0.01047', '0.003223', '-0.00883', '-0.00989', '0.03113', '0.003668', '-0.01747', '0.00651', '0.004517', '0.003813', '-0.002302', '0.01406', '-0.01622', '0.007645', '0.02664', '0.01695', '-0.02127', '0.03008', '-0.001394', '0.00815', '-0.001634', '-0.01892', '0.01033', '0.01499', '0.004833', '-0.004704', '-0.012054', '-0.007492', '-0.001868', '-0.008644', '-0.00417', '0.02376', '-0.005035', '0.00199', '0.004314', '0.0148', '0.02493', '0.01347', '-0.000257', '0.02954', '-0.003366', '0.0096', '0.0446', '0.00952', '0.00571', '-0.0017185', '0.00549', '0.0158']",,,,,,,
mondo:0033483,"erythrocytosis, familial, 5","['ECYT5', 'familial polycythemia caused by mutation in EPO', 'EPO familial polycythemia', 'familial erythrocytosis 5', 'erythrocytosis, familial, 5']",0080290,617907,,CN873435,,,,,,,,
mondo:0033485,short-rib thoracic dysplasia 19 with or without polydactyly,"['short-rib thoracic dysplasia 19 with or without polydactyly', 'SRTD19']",0080295,617895,,CN842245,,,,,,,,
mondo:0033486,"leukodystrophy, hypomyelinating, 14","['leukodystrophy, hypomyelinating, 14', 'HLD14', 'hypomyelinating leukodystrophy 14']",0080296,617899,,CN845004,,,,,,,,
mondo:0033492,Coffin-Siris syndrome 6,"['CSS6', 'ARID2-related BAFopathy', 'COFFIN-SIRIS syndrome 6']",0080297,617808,1465,CN696018,"['0.1471', '-0.01811', '0.3162', '-0.4443', '0.3696', '-0.456', '0.7373', '1.09', '-0.1963', '-0.2627', '-0.2878', '-0.3655', '0.00238', '0.1619', '-0.3176', '0.6577', '0.3667', '-0.5693', '-0.3647', '-0.727', '-0.3582', '0.4133', '0.3794', '0.11566', '-0.1176', '-0.374', '0.1511', '0.4478', '0.5444', '-0.4558', '0.4285', '-0.01674', '-0.2551', '0.1545', '-0.1989', '-0.0596', '-0.573', '-0.3953', '-0.612', '-0.4417', '0.05844', '0.01232', '0.1702', '0.10614', '0.3022', '-0.7646', '-0.05313', '0.56', '-0.1694', '-0.2388', '-0.3838', '0.1333', '-0.0888', '-0.1886', '-0.7827', '-0.683', '-0.0331', '-0.1106', '-0.1271', '0.004944', '0.02992', '0.1823', '0.3013', '0.2494', '-0.1209', '0.05646', '0.02892', '0.1263', '-0.434', '0.397', '-0.1948', '0.3882', '-0.4429', '0.346', '0.00455', '0.1853', '0.6797', '-1.074', '-0.2764', '-0.3645', '0.4197', '-0.1279', '0.1586', '0.4707', '0.3157', '0.4417', '-0.0797', '0.4612', '0.1619', '0.1383', '0.3428', '0.7964', '-0.1559', '0.2942', '0.251', '-0.219', '0.1895', '-0.2189', '0.6475', '0.5654']",,,,,,,
mondo:0033493,"fibromatosis, gingival, 5","['gingival fibromatosis 5', 'GINGF5', 'fibromatosis, gingival, 5', 'GGF5', 'fibromatosis, gingival, hereditary, 5']",0080280,617626,,,,,,,,,,
mondo:0033532,Suleiman-El-Hattab syndrome,"['SULEHS', 'SULEIMAN-EL-HATTAB SYNDROME']",,618950,,,,,,,,,,
mondo:0033533,combined oxidative phosphorylation deficiency 45,"['COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 45', 'COXPD45']",0112113,618951,,,,,,,,,,
mondo:0033534,combined oxidative phosphorylation deficiency 46,"['COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 46', 'combined oxidative phosphorylation defiency 46', 'COXPD46']",0112115,618952,,,,,,,,,,
mondo:0033537,combined oxidative phosphorylation deficiency 47,"['COXPD47', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 47']",0112114,618958,,,,,,,,,,
mondo:0033541,immunodeficiency 69,"['immunodeficiency 69, mycobacteriosis', 'Immunodeficiency 69, Mycobacteriosis, Autosomal Recessive', 'IMMUNODEFICIENCY 69', 'IMD69', 'Ifng Deficiency, Autosomal Recessive']",0112006,618963,,,,,,,,,,
mondo:0033542,immunodeficiency 70,"['IMD70', 'IMMUNODEFICIENCY 70']",0112005,618969,,,,,,,,,,
mondo:0033543,"cone-rod synaptic disorder syndrome, congenital nonprogressive","['CRSDS', 'CONE-ROD SYNAPTIC DISORDER SYNDROME, CONGENITAL NONPROGRESSIVE']",,618970,,,,,,,,,,
mondo:0033544,Tolchin-Le Caignec syndrome,"['TOLCHIN-LE CAIGNEC SYNDROME', 'TOLCAS', 'intellectual developmental disorder With behavioral abnormalities and variable bone defects', 'intellectual developmental disorder With behavioural abnormalities and variable bone defects']",,618971,,,,,,,,,,
mondo:0033545,mitochondrial DNA depletion syndrome 19,"['MITOCHONDRIAL DNA DEPLETION SYNDROME 19', 'MTDPS19']",,618972,,,,,,,,,,
mondo:0033546,"neurodegeneration, infantile-onset, biotin-responsive","['Sodium-Dependent Multivitamin Transporter Deficiency', 'NEURODEGENERATION, INFANTILE-ONSET, BIOTIN-RESPONSIVE', 'Smvt Deficiency', 'NERIB']",,618973,,,,,,,,,,
mondo:0033547,Li-Ghorbani-Weisz-Hubshman syndrome,"['Li-Ghorgani-Weisz-Hubshman syndrome', 'LI-GHORBANI-WEISZ-HUBSHMAN SYNDROME', 'LIGOWS']",,618974,,,,,,,,,,
mondo:0033548,"myopathy, congenital, with diaphragmatic defects, respiratory insufficiency, and dysmorphic facies","['MYODRIF', 'Myopathy, Congenital, Due to Myod1 Deficiency', 'MYOPATHY, CONGENITAL, WITH DIAPHRAGMATIC DEFECTS, RESPIRATORY INSUFFICIENCY, AND DYSMORPHIC FACIES']",0081349,618975,,,,,,,,,,
mondo:0033549,optic atrophy 12,"['OPA12', 'OPTIC ATROPHY 12']",0080840,618977,,,,,,,,,,
mondo:0033551,immunodeficiency 72 with autoinflammation,"['IMD72', 'IMMUNODEFICIENCY 72 WITH AUTOINFLAMMATION']",0112015,618982,,,,,,,,,,
mondo:0033554,immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia,"['immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia', 'IMD73B']",0112061,618986,,,,,,,,,,
mondo:0033555,immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia,"['IMD73C', 'IMMUNODEFICIENCY 73C WITH DEFECTIVE NEUTROPHIL CHEMOTAXIS AND HYPOGAMMAGLOBULINEMIA']",0112062,618987,,,,,,,,,,
mondo:0033556,"muscular dystrophy-dystroglycanopathy (congenital with impaired intellectual development), type b, 15","['Muscular Dystrophy, Congenital, Dpm3-Related', 'MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH IMPAIRED INTELLECTUAL DEVELOPMENT), TYPE B, 15', 'MDDGB15']",0112376,618992,,,,,,,,,,
mondo:0033557,"hemophagocytic lymphohistiocytosis, familial, 6","['immune dysregulation and systemic hyperinflammation syndrome', 'HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS, FAMILIAL, 6', 'FHL6']",,618998,,,,,,,,,,
mondo:0033558,"autoinflammation, immune dysregulation, and eosinophilia","['AIIDE', 'AUTOINFLAMMATION, IMMUNE DYSREGULATION, AND EOSINOPHILIA', 'Atopic Dermatitis, Enteritis, Colitis, and Eosinophilia']",,618999,,,,,,,,,,
mondo:0033559,intellectual developmental disorder with seizures and language delay,"['INTELLECTUAL DEVELOPMENTAL DISORDER WITH SEIZURES AND LANGUAGE DELAY', 'IDDSELD']",,619000,,,,,,,,,,
mondo:0033560,"mitochondrial complex 1 deficiency, nuclear type 35","['MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 35', 'MC1DN35']",0112139,619003,,,,,,,,,,
mondo:0033561,deeah syndrome,"['Developmental Delay With Endocrine, Exocrine, Autonomic, and Hematologic Abnormalities', 'DEEAH', 'DEEAH SYNDROME']",,619004,,,,,,,,,,
mondo:0033562,"neurodevelopmental disorder with dysmorphic facies, impaired speech, and hypotonia","['NEURODEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES, IMPAIRED SPEECH, AND HYPOTONIA', 'NEDDISH', 'neurodevelopmental disorder with dysmorphic facies, impaired speech and hypotonia']",,619005,,,,,,,,,,
mondo:0033563,retinitis pigmentosa 90,"['RETINITIS PIGMENTOSA 90', 'RP90']",0112147,619007,,,,,,,,,,
mondo:0033564,oocyte maturation defect 8,"['OOCYTE MATURATION DEFECT 8', 'OOMD8']",,619009,,,,,,,,,,
mondo:0033565,oocyte maturation defect 9,"['OOCYTE MATURATION DEFECT 9', 'OOMD9']",,619011,,,,,,,,,,
mondo:0033566,combined oxidative phosphorylation deficiency 48,"['COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48', 'COXPD48']",0112112,619012,,,,,,,,,,
mondo:0033569,combined oxidative phosphorylation deficiency 49,"['COXPD49', 'COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 49']",0112110,619024,,,,,,,,,,
mondo:0033570,combined oxidative phosphorylation deficiency 50,"['COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 50', 'COXPD50']",0112111,619025,,,,,,,,,,
mondo:0033572,"intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies","['INTELLECTUAL DEVELOPMENTAL DISORDER WITH EPILEPSY, BEHAVIORAL ABNORMALITIES, AND COARSE FACIES', 'IDDEBF']",,619031,,,,,,,,,,
mondo:0033613,neurodevelopmental disorder with progressive spasticity and brain white matter abnormalities,"['cerebral palsy, spastic quadriplegic, type 1', 'infantile neurodegeneration-progressive spasticity-intellectual disability-white matter lesions syndrome', 'cerebral palsy spastic quadriplegic', 'cerebral palsy, spastic quadriplegic, 1', 'CPSQ1', 'NEDSWMA']",,619026,641353,C2751938,,,,C567853,,,,
mondo:0033614,"spastic paraplegia 83, autosomal recessive",['SPG83'],0112346,619027,,,,,,,,,,
mondo:0033615,"coenzyme q10 deficiency, primary, 9",['COQ10D9'],0112138,619028,,,,,,,,,,
mondo:0033618,Vissers-Bodmer syndrome,['VIBOS'],,619033,,,,,,,,,,
mondo:0033619,"myopathy, epilepsy, and progressive cerebral atrophy",['MEPCA'],,619036,,,,,,,,,,
mondo:0033620,myofibrillar myopathy 10,['MFM10'],0112108,619040,,,,,,,,,,
mondo:0033621,"spinal muscular atrophy, infantile, James type",['SMAJI'],,619042,,,,,,,,,,
mondo:0033622,spermatogenic failure 44,['SPGF44'],0112109,619044,,,,,,,,,,
mondo:0033630,neurodevelopmental disorder with speech impairment and dysmorphic facies,['NEDSID'],0070417,619056,,,,,,,,,,
mondo:0033631,combined oxidative phosphorylation deficiency 51,['COXPD51'],0112137,619057,,,,,,,,,,
mondo:0033635,"mitochondrial complex 4 deficiency, nuclear type 3","['mitochondrial complex IV deficiency, nuclear type 3', 'MC4DN3']",,619046,,,,,,,,,,
mondo:0033636,"mitochondrial complex 4 deficiency, nuclear type 4","['MC4DN4', 'mitochondrial complex IV deficiency, nuclear type 4']",,619048,,,,,,,,,,
mondo:0033637,"mitochondrial complex 4 deficiency, nuclear type 7","['MC4DN7', 'mitochondrial complex IV deficiency, nuclear type 7']",,619051,,,,,,,,,,
mondo:0033638,"mitochondrial complex 4 deficiency, nuclear type 8","['MC4DN8', 'mitochondrial complex IV deficiency, nuclear type 8']",,619052,,,,,,,,,,
mondo:0033639,"mitochondrial complex 4 deficiency, nuclear type 10","['mitochondrial complex IV deficiency, nuclear type 10', 'MC4DN10']",,619053,,,,,,,,,,
mondo:0033640,"vitamin D-dependent rickets, type 3",['VDDR3'],,619073,,,,,,,,,,
mondo:0033641,"cleft palate, proliferative retinopathy, and developmental delay",['CPPRDD'],,619074,,,,,,,,,,
mondo:0033642,neurodevelopmental disorder with alopecia and brain abnormalities,"['global developmental delay-alopecia-macrocephaly-facial dysmorphism-structural brain anomalies syndrome', 'NEDABA', 'Bachmann-Bupp syndrome']",,619075,544488,,,,,,,,,
mondo:0033643,inflammatory bowel disease 30,"['IBD30', 'inflammatory bowel disease (Crohn disease) 30']",0112154,619079,,,,,,,,,,
mondo:0033644,"microcornea, rod-cone dystrophy, cataract, and posterior staphyloma 1",['MRCS1'],,619082,,,,,,,,,,
mondo:0033645,"mitochondrial complex 4 deficiency, nuclear type 11","['mitochondrial complex IV deficiency, nuclear type 11', 'MC4DN11']",,619054,,,,,,,,,,
mondo:0033646,"mitochondrial complex 4 deficiency, nuclear type 12","['MC4DN12', 'mitochondrial complex IV deficiency, nuclear type 12']",,619055,,,,,,,,,,
mondo:0033649,"mitochondrial complex 4 deficiency, nuclear type 14","['MC4DN14', 'mitochondrial complex IV deficiency, nuclear type 14']",,619058,,,,,,,,,,
mondo:0033650,"mitochondrial complex 4 deficiency, nuclear type 15","['MC4DN15', 'mitochondrial complex IV deficiency, nuclear type 15']",,619059,,,,,,,,,,
mondo:0033651,"mitochondrial complex 4 deficiency, nuclear type 16","['MC4DN16', 'mitochondrial complex IV deficiency, nuclear type 16']",,619060,,,,,,,,,,
mondo:0033652,"mitochondrial complex 4 deficiency, nuclear type 17","['mitochondrial complex IV deficiency, nuclear type 17', 'MC4DN17']",,619061,,,,,,,,,,
mondo:0033653,"mitochondrial complex 4 deficiency, nuclear type 18","['MC4DN18', 'mitochondrial complex IV deficiency, nuclear type 18']",,619062,,,,,,,,,,
mondo:0033654,"mitochondrial complex 4 deficiency, nuclear type 19","['MC4DN19', 'mitochondrial complex IV deficiency, nuclear type 19']",,619063,,,,,,,,,,
mondo:0033655,"mitochondrial complex 4 deficiency, nuclear type 20","['mitochondrial complex IV deficiency, nuclear type 20', 'MC4DN20']",,619064,,,,,,,,,,
mondo:0033656,"mitochondrial complex 4 deficiency, nuclear type 21","['mitochondrial complex IV deficiency, nuclear type 21', 'MC4DN21']",,619065,,,,,,,,,,
mondo:0033657,"leukodystrophy, hypomyelinating, 20",['HLD20'],0112153,619071,,,,,,,,,,
mondo:0033658,neurodevelopmental disorder with seizures and brain atrophy,['NEDSEBA'],,619072,,,,,,,,,,
mondo:0033662,"neurodevelopmental disorder with microcephaly, seizures, and brain atrophy",['NEDMISB'],,619076,,,,,,,,,,
mondo:0033664,Kilquist syndrome,['KILQS'],,619080,,,,,,,,,,
mondo:0033665,"hearing loss, autosomal dominant 78","['DFNA78', 'deafness, autosomal dominant 78']",0112159,619081,,,,,,,,,,
mondo:0033667,Delpire-McNeill syndrome,['DELMNES'],,619083,,,,,,,,,,
mondo:0033668,"hearing loss, autosomal dominant 79","['deafness, autosomal dominant 79', 'DFNA79']",0112160,619086,,,,,,,,,,
mondo:0033669,Noonan syndrome 13,['NS13'],0112161,619087,,,,C177121,,,,,,
mondo:0033670,"hearing loss, autosomal recessive 116","['deafness, autosomal recessive 116', 'DFNB116']",0112162,619093,,,,,,,,,,
mondo:0033671,spermatogenic failure 45,['SPGF45'],0112163,619094,,,,,,,,,,
mondo:0033672,Duane anomaly-myopathy-scoliosis syndrome,,,,50817,,,,,,,,,
mondo:0033673,spermatogenic failure 46,['SPGF46'],0112164,619095,,,,,,,,,,
mondo:0033682,skeletal dysplasia-T-cell immunodeficiency-developmental delay syndrome,,,,508533,,,,,,,,,
mondo:0033683,congenital progressive bone marrow failure-B-cell immunodeficiency-skeletal dysplasia syndrome,['MYSM1 deficiency'],,,508542,,,,,,,,,
mondo:0033717,congenital cerebellar ataxia due to RNU12 mutation,,,,512260,,,,,,,,,
mondo:0033809,isolated blepharochalasis,,,,519390,,,,,,,,,
mondo:0033810,isolated iridoschisis,,,,519392,,,,,,,,,
mondo:0033816,thygeson superficial punctate keratopathy,,,,519406,,,,,,,,,
mondo:0033818,Terrien marginal degeneration,['Terrien^s marginal degeneration'],,,519410,,,,,,,,,
mondo:0033821,fungal keratitis,,,,519930,,,C128370,,,,,,
mondo:0033838,radiation-induced plexopathy,,,,521123,,,,,,,,,
mondo:0033839,osteoradionecrosis of the mandible,,,,521127,,,,,,,,,
mondo:0033850,autosomal recessive axonal charcot-marie-tooth disease due to copper metabolism defect,,,,521411,,,,,,,,,
mondo:0033853,congenital cataract-severe neonatal hepatopathy-global developmental delay syndrome,,,,521432,,,,,,,,,
mondo:0033856,LAMA5-related multisystemic syndrome,,,,521450,,,,,,,,,
mondo:0033862,primary autoimmune enteropathy,,,,522037,,,,,,,,,
mondo:0033864,infantile hypotonia-oculomotor anomalies-hyperkinetic movements-developmental delay syndrome,['Baker-Gordon syndrome'],,618218,522077,,"['-0.26', '0.0259', '0.4521', '-0.2029', '-0.1678', '-0.1903', '0.2466', '0.4084', '-0.2487', '-0.1005', '-0.2133', '-0.2617', '-0.03476', '-0.2451', '0.0531', '0.0096', '0.1266', '-0.3818', '-0.307', '-0.6353', '0.1581', '0.185', '0.1016', '-0.1935', '0.0485', '-0.1819', '-0.1414', '-0.1559', '0.1454', '-0.0733', '0.2091', '0.02449', '0.575', '0.2056', '0.06573', '0.02243', '-0.0511', '-0.4395', '-0.08484', '-0.2646', '0.4316', '-0.4224', '-0.043', '-0.0694', '0.0607', '-0.3018', '-0.1436', '0.2805', '-0.3252', '0.1993', '-0.3855', '0.533', '-0.1343', '-0.2715', '0.183', '-0.1393', '0.1343', '-0.1021', '-0.1833', '0.237', '0.0239', '-0.1499', '0.02208', '0.04865', '-0.3281', '0.04175', '0.2725', '0.3447', '-0.3113', '0.2607', '-0.3782', '0.1103', '-0.09766', '0.0203', '-0.05487', '-0.0916', '0.4536', '-0.3267', '-0.2544', '-0.05664', '0.2157', '0.0869', '-0.0677', '0.6353', '0.12225', '0.1212', '0.02785', '0.3987', '0.5117', '0.2507', '0.2485', '0.483', '0.0323', '0.2', '0.2595', '0.1892', '0.4592', '-0.1021', '0.4158', '0.1982']",,,,,,,
mondo:0033885,"mitochondrial complex IV deficiency, nuclear-type",,,,,,,,,,,,,
mondo:0033925,pediatric-onset Graves disease,,,,525731,,,,,,,,,
mondo:0033926,prepubertal anorexia nervosa,,,,525738,,,,,,,,,
mondo:0033938,acute radiation syndrome,['Acute radiation sickness'],,,454831,,,,,D054508,,,,
mondo:0033946,hereditary angioedema with C1Inh deficiency,"['HAE1', 'angioedema, hereditary, type 1', 'angioneurotic edema, hereditary', 'angioedema, hereditary, type 2', 'angioedema, hereditary, 1 and 2', 'C1 esterase inhibitor, deficiency of', 'angioedema, hereditary, type I', 'angioedema, hereditary, type 1/2']",0080939,106100,528623,,,,,,,,,
mondo:0033947,hereditary angioedema with normal C1Inh,,,,528647,,,,,,,,,
mondo:0033948,acquired angioedema with C1Inh deficiency,,,,528663,,,,,,,,,
mondo:0033954,monoclonal mast cell activation syndrome,,,,529468,,,C181652,,,,,,
mondo:0033968,immune dysregulation-inflammatory bowel disease-arthritis-recurrent infections-lymphopenia syndrome,,,,529977,,,,,,,,,
mondo:0033969,inflammatory bowel disease-recurrent sinopulmonary infections syndrome,,,,529980,,,,,,,,,
mondo:0033980,RELA fusion-positive ependymoma,,0080892,,530792,,,,,,,,,
mondo:0034021,spondylodysplastic Ehlers-Danlos syndrome,['spondylodysplastic EDS'],,,536471,,,,,,,,,
mondo:0034022,Bethlem myopathy 2,"['Bethlem myopathy caused by mutation in COL12A1', 'EDS, myopathic type', 'COL12A1 Bethlem myopathy', 'Bethlem myopathy 2', 'Bethlem myopathy type 2', 'myopathic EDS', 'Ehlers-Danlos syndrome, myopathic type', 'myopathic Ehlers-Danlos syndrome', 'BTHLM2']",,616471,536516,C4225313,,,,,,,,
mondo:0034024,kyphoscoliotic Ehlers-Danlos syndrome,"['EDS VI', 'kyphoscoliotic EDS']",,,536545,,,,,,,,,
mondo:0034041,congenital axonal neuropathy with encephalopathy,,,,538101,,,,,,,,,
mondo:0034054,severe combined immunodeficiency due to CD70 deficiency,['lymphoproliferative syndrome 3'],,618261,538958,,,,,,,,,
mondo:0034092,optic atrophy-ataxia-peripheral neuropathy-global developmental delay syndrome,,,,543470,,,,,,,,,
mondo:0034099,SYNGAP1-related developmental and epileptic encephalopathy,,,,544254,,,,,,,,,
mondo:0034103,infection-related hemolytic uremic syndrome,,,,544482,,,,,,,,,
mondo:0034106,"developmental and epileptic encephalopathy, 73","['DEE73', 'developmental and epileptic encephalopathy 73', 'rnf13-related severe early-onset epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 73']",0112209,618379,544503,,,,,,,,,
mondo:0034109,congenital myopathy with reduced type 2 muscle fibers,"['myopathy, congenital, with fast-twitch (type II) fiber atrophy', 'myopathy, congenital, with fast-twitch (type II) fibre atrophy']",0081346,618414,544602,,,,,,,,,
mondo:0034110,atypical Fanconi syndrome-neonatal hyperinsulinism syndrome,,,,544628,,,,,,,,,
mondo:0034121,NAD(P)HX dehydratase deficiency,"['ENCEPHALOPATHY, PROGRESSIVE, EARLY-ONSET, WITH BRAIN EDEMA AND/OR LEUKOENCEPHALOPATHY, 2', 'PEBEL2']",,618321,555402,,,,,,,,,
mondo:0034127,IgA pemphigus,,0080851,,555905,,,,,,,,,
mondo:0034142,pancreatic agenesis-holoprosencephaly syndrome,,,,556955,,,,,,,,,
mondo:0034143,early-onset calcifying leukoencephalopathy-skeletal dysplasia,,,,556985,,,,,,,,,
mondo:0034145,oculocerebrodental syndrome,"['Cataracts, Early-Onset, With Skeletal and Dental Anomalies', 'OCSKD', 'oculoskeletodental syndrome']",,618440,557003,,,,,,,,,
mondo:0034146,spastic ataxia-dysarthria due to glutaminase deficiency,,,,557056,,,,,,,,,
mondo:0034150,idiopathic gastroparesis,,,,558411,,,,,,,,,
mondo:0034186,autosomal recessive extra-oral halitosis,,,,562538,,,,,,,,,
mondo:0034189,primary biliary cholangitis/primary sclerosing cholangitis and autoimmune hepatitis overlap syndrome,,,,562639,,,,,,,,,
mondo:0034204,syndromic congenital sodium diarrhea,,,,563708,,,,,,,,,
mondo:0034212,methotrexate toxicity,,,,565782,,,,,,,,,
mondo:0034216,resistance to thyroid hormone due to a mutation in thyroid hormone receptor alpha,['resistance to thyroid hormone alpha'],,,566231,,,,,,,,,
mondo:0034217,resistance to thyroid hormone due to a mutation in thyroid hormone receptor beta,,,,566243,,,,,,,,,
mondo:0034556,vibratory angioedema,,,,493348,,,,,,,,,
mondo:0034661,syndromic biliary atresia,,,,498350,,,,,,,,,
mondo:0034669,non-syndromic preaxial polydactyly,,,,498464,,,,,,,,,
mondo:0034670,non-syndromic postaxial polydactyly,,,,498467,,,,,,,,,
mondo:0034671,non-syndromic complex polydactyly,,,,498470,,,,,,,,,
mondo:0034676,overgrowth syndrome with 2q37 translocation,,,,498488,,,,,,,,,
mondo:0034820,cleft lip and palate-craniofacial dysmorphism-congenital heart defect-hearing loss syndrome,"['cleft lip and palate-craniofacial dysmorphism-congenital heart defect-deafness syndrome', 'hyaluronidase 2 deficiency']",,,508476,,,,,,,,,
mondo:0034823,oral-facial-digital syndrome with short stature and brachymesophalangy,"['orofaciodigital syndrome type 18', 'OFD18', 'oral-facial-digital syndrome type 18']",,,508501,,,,,,,,,
mondo:0034846,primary desmosis coli,,,,565641,,,,,,,,,
mondo:0034872,large granular lymphocyte leukemia,,,,512034,,,,,,,,,
mondo:0034895,congenital brachyesophagus-intrathoracic stomach-vertebral anomalies syndrome,['serpentine-like syndrome'],,,514352,,,,,,,,,
mondo:0034901,ATP13A2-related parkinsonism,,,,514980,,,,,,,,,
mondo:0034954,syndromic vitreoretinopathy,,,,519327,,,,,,,,,
mondo:0034971,isolated congenital entropion,,,,519386,,,,,,,,,
mondo:0034976,iatrogenic Creutzfeldt-Jakob disease,,,,576379,,,,,,,,,
mondo:0034978,isolated foveal hypoplasia,,,,519398,,,,,,,H35.8,,
mondo:0034987,intraductal tubulopapillary neoplasm of pancreas,,,,580572,,,,,,,,,
mondo:0034989,intellectual disability-cardiac anomalies-short stature-joint laxity syndrome,,,,508498,,,,,,,,,
mondo:0034991,intrauterine growth restriction-congenital multiple café-au-lait macules-increased sister chromatid exchange syndrome,,,,508512,,,,,,,,,
mondo:0035002,isolated inherited retinal disorder,,,,520817,,,,,,,,,
mondo:0035004,"serine biosynthesis pathway deficiency, infantile/juvenile form",,,,583595,,,,,,,,,
mondo:0035008,isolated splenic vein thrombosis,,,,583856,,,,,,,,,
mondo:0035009,isolated mesenteric vein thrombosis,,,,583861,,,,,,,,,
mondo:0035014,primary orthostatic disorder,,,,521236,,,,,,,,,
mondo:0035018,frontonasal dysplasia-bifid nose-upper limb anomalies syndrome,,,,521308,,,,,,,,,
mondo:0035027,microcephaly-facial dysmorphism-ocular anomalies-multiple congenital anomalies syndrome,,,,521445,,,,,,,,,
mondo:0035075,secondary early-onset glaucoma of genetic origin,,,,522580,,,,,,,,,
mondo:0035105,diaphragmatic hernia-short bowel-asplenia syndrome,,,,527468,,,,,,,,,
mondo:0035112,acute myeloid leukemia with BCR-ABL1,"['AML with t(9;22)(q34.1;q11.2)', 'AML with BCR-ABL1', 'acute myeloid leukaemia with t(9;22)(q34.1;q11.2)']",0080976,,585867,,,C129785,,,,,,
mondo:0035117,PUM1-associated developmental disability-ataxia-seizure syndrome,,,,589515,,,,,,,,,
mondo:0035121,myeloid/lymphoid neoplasm associated with JAK2 rearrangement,['myeloid/lymphoid neoplasms with PCM1-JAK2'],,,589542,,,C129853,,,,,,
mondo:0035122,"GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder",,,,589547,,,,,,,,,
mondo:0035124,"linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies",,,,589608,,,,,,,,,
mondo:0035133,PHIP-related behavioral problems-intellectual disability-obesity-dysmorphic features syndrome,"['developmental delay, intellectual disability, obesity, and dysmorphic features', 'Chung-Jansen syndrome', 'DIDOD']",,617991,589905,CN248510,,,,,,,,
mondo:0035136,isolated melanotic schwannoma,,,,590539,,,,,,,,,
mondo:0035149,secondary erythromelalgia,['Secondary erythermalgia'],,,529864,,,,,,,I73.8,,
mondo:0035151,17q24.2 microdeletion syndrome,['Del(17)(q24)'],,,529962,,,,,,,,,
mondo:0035153,male infertility due to acephalic spermatozoa,['Acephalic spermatozoa syndrome'],0112311,,529970,,,,,,,N46,,
mondo:0035159,dermoid or epidermoid cyst of the central nervous system,['Dermoid or epidermoid cyst of the CNS'],,,530033,,,,,,,Q07.8,,
mondo:0035160,progressive myoclonic epilepsy with neuroserpin inclusion bodies,['early onset familial encephalopathy with neuroserpin inclusion bodies'],,,530298,,,,,,,G40.3,,
mondo:0035161,progressive dementia with neuroserpin inclusion bodies,['late-onset familial encephalopathy with neuroserpin inclusion bodies'],,,530303,,,,,,,G40.3,,
mondo:0035162,PIK3CA-related overgrowth syndrome,['PROS'],,,530313,,,,,,,,,
mondo:0035173,9q21.13 microdeletion syndrome,,,,531151,,,,,,,F78.1,,
mondo:0035220,PLG-related hereditary angioedema with normal C1inh,['PLG-related HAE with normal C1 inhibitor'],,,537072,,,,,,,D84.1,,
mondo:0035235,classic pyoderma gangrenosum,['Ulcerative pyoderma gangrenosum'],,,538863,,,,,,,L88,,
mondo:0035236,pustular pyoderma gangrenosum,,,,538866,,,,,,,L88,,
mondo:0035237,bullous pyoderma gangrenosum,['Phemphigoid pyoderma gangrenosum'],,,538869,,,,,,,L88,,
mondo:0035238,vegetative pyoderma gangrenosum,['Granulomatous pyoderma gangrenosum'],,,538872,,,,,,,L88,,
mondo:0035290,atypical hemolytic uremic syndrome with complement gene abnormality,"['Atypical HUS with complement gene abnormality', 'aHUS with complement gene abnormality']",,,544472,,,,,,,D58.8,,
mondo:0035293,streptococcus pneumoniae-associated hemolytic uremic syndrome,"['S. pneumoniae-associated HUS', 'SP-HUS']",,,544493,,,,,,,D58.8,,
mondo:0035295,"congenital primary megaureter, refluxing and obstructed form",,,,544578,,,,,,,Q62.2,,
mondo:0035312,fibrohistiocytic inflammatory pseudotumor of the liver,,,,555434,,,,,,,K75.8,,
mondo:0035313,lymphoplasmacytic inflammatory pseudotumor of the liver,['IgG4-related inflammatory pseudotumor of the liver'],,,555437,,,,,,,K75.8,,
mondo:0035320,early-onset familial hypoaldosteronism,"['Early-onset familial hyperreninemic hypoaldosteronism', 'Severe aldosterone synthase deficiency']",,,556030,,,,,,,E27.4,,
mondo:0035321,late-onset familial hypoaldosteronism,"['Late-onset familial hyperreninemic hypoaldosteronism', 'Mild aldosterone synthase deficiency']",,,556037,,,,,,,E27.4,,
mondo:0035337,Duane retraction syndrome with congenital deafness,"['DRS with hearing loss', 'DRS with deafness', 'DURS with deafness', 'DURS with hearing loss', 'Duane retraction syndrome with congenital hearing loss']",,,529574,,,,,,,,,
mondo:0035344,acute bilirubin encephalopathy,"['ABE', 'Acute kernicterus']",,,529799,,,,,,,,,
mondo:0035345,chronic bilirubin encephalopathy,"['KSD', 'Bilirubin-induced neurological dysfunction', 'CBE', 'Kernicterus spectrum disorder', 'BIND']",,,529808,,,,,,,,,
mondo:0035349,localized dystrophic epidermolysis bullosa,"['localised DEB', 'localized DEB']",,,595356,,,,,,,,,
mondo:0035350,letrozole toxicity,,,,529831,,,,,,,,,
mondo:0035357,portosinusoidal vascular disease,['PSVD'],,,596937,,,,,,,,,
mondo:0035362,TRIM22-related inflammatory bowel disease,['TRIM22-related IBD'],,,597201,,,,,,,,,
mondo:0035370,ALPI-related inflammatory bowel disease,,,,597887,,,,,,,,,
mondo:0035375,multisystem inflammatory syndrome in children and adults,['MIS-C/A'],,,598363,,,,,,,,,
mondo:0035383,FOXG1 syndrome,['FOXG1-related epileptic-dyskinetic encephalopathy'],,,561854,,,,,,,F84.8,,
mondo:0035400,seronegative autoimmune hepatitis,"['autoantibody-negative autoimmune hepatitis', 'Seronegative AIH']",,,563589,,,,,,,K75.4,,
mondo:0035401,isolated anencephaly,,,,563609,,,,,,,Q00.0,,
mondo:0035402,isolated exencephaly,,,,563612,,,,,,,Q00.0,,
mondo:0035403,serous cystadenoma of childhood,['Serous cystadenoma of ovary in childhood'],,,563666,,,,,,,D27,,
mondo:0035404,mucinous cystadenoma of childhood,['Mucinous cystadenoma of ovary in childhood'],,,563671,,,,,,,D27,,
mondo:0035405,seromucinous cystadenoma of childhood,['Seromucinous cystadenoma of ovary in childhood'],,,563676,,,,,,,D27,,
mondo:0035406,furuncular myiasis due to Dermatobia hominis,"['furunculoid myiasis due to Dermatobia hominis', 'furunculous myiasis due to Dermatobia hominis']",,,563684,,,,,,,B87.0,,
mondo:0035407,furuncular myiasis due to Cordylobia anthropophaga,"['furunculous myiasis due to Cordylobia anthropophaga', 'furunculoid myiasis due to Cordylobia anthropophaga']",,,563687,,,,,,,B87.0,,
mondo:0035408,furuncular myiasis due to Cordylobia rodhaini,"['furunculoid myiasis due to Cordylobia rodhaini', 'furunculous myiasis due to Cordylobia rodhaini']",,,563690,,,,,,,B87.0,,
mondo:0035410,isolated congenital aglossia,,,,563951,,,,,,,Q38.3,,
mondo:0035411,isolated congenital hypoglossia,,,,563954,,,,,,,Q38.3,,
mondo:0035423,triglyceride deposit cardiomyovasculopathy,"['Neutral lipid storage disease with severe cardiovascular involvement', 'TGCV']",,,565612,,,,,,,E75.5,,
mondo:0035432,POMGNT2-related limb-girdle muscular dystrophy R24,"['POMGNT2-related LGMD R24', 'POMGNT2-related muscular dystrophy', 'LGMD type R24', 'limb-girdle muscular dystrophy type R24']",,,565899,,,,,,,G71.0,,
mondo:0035433,calpain-3-related limb-girdle muscular dystrophy D4,"['limb-girdle muscular dystrophy type D4', 'LGMD type D4', 'LGMD1I', 'calpain-3-related LGMD D4']",,,565909,,,,,,,G71.0,,
mondo:0035437,CEBPE-associated autoinflammation-immunodeficiency-neutrophil dysfunction syndrome,['CAIN'],,,566067,,,,,,,D89.8,,
mondo:0035441,congenital autosomal recessive small-platelet thrombocytopenia,['CARST'],,,566192,,,,,,,D69.4,,
mondo:0035444,acute mast cell leukemia,['Acute MCL'],,,566393,,,,,,,C94.3,,
mondo:0035445,chronic mast cell leukemia,['Chronic MCL'],,,566396,,,,,,,C94.3,,
mondo:0035447,liver adenomatosis,['Hepatic adenomatosis'],,,566841,,,,,,,D13.4,,
mondo:0035449,atelencephaly,['atelencephalic microcephaly'],,,566852,,,,,,,,,
mondo:0035450,aprosencephaly,,,,566857,,,C98824,,,,,,
mondo:0035452,mueller-weiss syndrome,"['Brailsford disease', 'Mueller-Weiss osteonecrosis of the tarsal bone']",,,566943,,,,,,,,,
mondo:0035454,B-cell immunodeficiency-limb anomaly-urogenital malformation syndrome,"['Hoffman syndrome', 'BILU syndrome']",,,567502,,,,,,,,,
mondo:0035459,idiopathic multidrug-resistant nephrotic syndrome,,,,567550,,,,,,,N04.8,,
mondo:0035460,idiopathic steroid-resistant nephrotic syndrome with sensitivity to second-line immunosuppressive therapy,['idiopathic steroid-resistant nephrotic syndrome with sensitivity to intensified immunosuppression'],,,567552,,,,,,,N04.8,,
mondo:0035472,GJC2-related late-onset primary lymphedema,,,,568051,,,,,,,,,
mondo:0035473,warts-immunodeficiency-lymphedema-anogenital dysplasia syndrome,"['WILD syndrome', 'disseminated warts-impaired cell-mediated immunity-primary lymphedema-anogenital dysplasia syndrome']",,,568056,,,,,,,,,
mondo:0035474,PIEZO1-related generalized lymphatic dysplasia with non-immune hydrops fetalis,"['PIEZO1-related lymphatic-related hydrops fetalis', 'generalised lymphatic dysplasia of Fotiou', 'generalized lymphatic dysplasia of Fotiou', 'PIEZO1-related generalised lymphatic dysplasia with systemic involvement', 'PIEZO1-related LRHF/GLD', 'PIEZO1-related generalized lymphatic dysplasia with systemic involvement']",,,568062,,,,,,,,,
mondo:0035475,EPHB4-related lymphatic-related hydrops fetalis,"['EPHB4-related generalised lymphatic dysplasia with non-immune hydrops fetalis', 'EPHB4-related generalized lymphatic dysplasia with atrial septal defect', 'EPHB4-related LRHF/GLD', 'EPHB4-related generalized lymphatic dysplasia with non-immune hydrops fetalis', 'EPHB4-related generalised lymphatic dysplasia with atrial septal defect']",,,568065,,,,,,,,,
mondo:0035499,CELSR1-related late-onset primary lymphedema,,,,569816,,,,,,,,,
mondo:0035500,congenital primary lymphedema of Gordon,['VEGFC-related congenital primary lymphedema'],,,569821,,,,,,,,,
mondo:0035511,ricin poisoning,,,,570470,,,,,,,T62.2,,
mondo:0035521,blepharophimosis-ptosis-epicanthus inversus syndrome plus,"['BPES plus', '3q23 microdeletion syndrome']",,,572333,,,,,,,,,
mondo:0035524,blepharophimosis-ptosis-epicanthus inversus syndrome type 1,"['blepharophimosis-ptosis-epicanthus inversus syndrome with premature ovarian failure', 'BPES type 1']",,,572354,,,,,,,,,
mondo:0035525,blepharophimosis-ptosis-epicanthus inversus syndrome type 2,"['BPES type 2', 'blepharophimosis-ptosis-epicanthus inversus syndrome without premature ovarian failure']",,,572361,,,,,,,,,
mondo:0035529,infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia,"['OAS1-related infantile-onset pulmonary alveolar proteinosis-hypogammaglobulinemia', 'OAS1 deficiency']",,,572428,,,,,,,,,
mondo:0035534,DONSON-related microcephaly-short stature-limb abnormalities spectrum,,,,572761,,,,,,,,,
mondo:0035540,pheochromocytoma-paraganglioma,,,,573163,,,,0020005,,,,,
mondo:0035547,predisposition to severe viral infection due to IRF7 deficiency,,,,574918,,,,,,,D84.8,,
mondo:0035548,autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial jak1 deficiency,['Autosomal recessive MSMD due to partial JAK1 deficiency'],,,574957,,,,,,,D84.8,,
mondo:0035551,cathepsin a-related arteriopathy-strokes-leukoencephalopathy,['CARASAL'],,,575553,,,,,,,I67.8,,
mondo:0035561,sporadic human prion disease,['idiopathic human prion disease'],,,576356,,,,,,,,,
mondo:0035562,acquired human prion disease,['infectious human prion disease'],,,576360,,,,,,,,,
mondo:0035584,punctate inner choroidopathy,,,,580951,,,,,,,H31.0,,
mondo:0035586,Cramp-fasciculation syndrome,,,,581271,,,,,,,G90.8,,
mondo:0035592,congenital infiltrating lipomatosis of the face,"['fibroadipose infiltrating lipomatosis', 'facial infused lipomatosis', 'CIL-F']",,,583097,,,,,,,Q87.3,,
mondo:0035605,B-lymphoblastic leukemia/lymphoma with recurrent genetic abnormality,,,,585877,,,C80328,,,,C91.0,,
mondo:0035614,sporadic fatal insomnia,,,,586130,,,,,,,A81.9,,
mondo:0035639,mixed phenotype acute leukemia with t(9;22)(q34.1;q11.2),['MPAL with t(9;22)(q34.1;q11.2); BCR-ABL1'],,,589534,,,,,,,C92.7,,
mondo:0035642,mixed phenotype acute leukemia with t(v;11q23.3),"['MPAL with t(v;11q23.3); KMT2A rearranged', 'MPAL with t(v;11q23.3); MLL rearranged']",,,589595,,,C82203,,,,C92.6,,
mondo:0035645,inherited gynecological cancer-predisposing syndrome,,,,589746,,,,,,,,,
mondo:0035646,congenital-onset Steinert myotonic dystrophy,"['Congenital-onset myotonic dystrophy type 1', 'Congenital-onset Steinert disease']",,,589821,,,,,,,G71.1,,
mondo:0035647,childhood-onset Steinert myotonic dystrophy,"['Childhood-onset Steinert disease', 'Childhood-onset myotonic dystrophy type 1']",,,589824,,,,,,,G71.1,,
mondo:0035648,juvenile-onset Steinert myotonic dystrophy,"['Juvenile-onset Steinert disease', 'Juvenile-onset myotonic dystrophy type 1']",,,589827,,,,,,,G71.1,,
mondo:0035649,adult-onset Steinert myotonic dystrophy,"['Adult-onset myotonic dystrophy type 1', 'Adult-onset Steinert disease']",,,589830,,,,,,,G71.1,,
mondo:0035650,late-onset Steinert myotonic dystrophy,"['Late-onset myotonic dystrophy type 1', 'Late-onset Steinert disease']",,,589833,,,,,,,G71.1,,
mondo:0035651,choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome,['KMT2D-related choanal atresia-athelia-hypothyroidism-delayed puberty-short stature syndrome'],,,589856,,,,,,,,,
mondo:0035660,GNAO1-related developmental delay-seizures-movement disorder spectrum,['GNAO1-related spectrum'],,,592564,,,,,,,F84.8,,
mondo:0035661,TRAF7-associated heart defect-digital anomalies-facial dysmorphism-motor and speech delay syndrome,,,,592570,,,,,,,,,
mondo:0035663,neuromyelitis optica spectrum disorder with anti-AQP4 antibodies,"['Neuromyelitis optica spectrum disorder with anti-aquaporin 4 antibodies', 'NMOSD with anti-AQP4 antibodies']",,,592850,,,,,,,G36.0,,
mondo:0035664,neuromyelitis optica spectrum disorder with anti-MOG antibodies,"['Neuromyelitis optica spectrum disorder with anti-myelin oligodendrocyte glycoprotein antibodies', 'NMOSD with anti-MOG antibodies']",,,592856,,,,,,,G36.0,,
mondo:0035665,neuromyelitis optica spectrum disorder without anti-MOG and without anti-AQP4 antibodies,"['Neuromyelitis optica spectrum disorder without anti-Myelin oligodendrocyte glycoprotein and without anti-Aquaporin-4 antibodies', 'NMOSD without anti-MOG antibodies and without anti-AQP4 antibodies']",,,592869,,,,,,,G36.0,,
mondo:0035666,acute transverse myelitis with anti-MOG antibodies,['Acute transverse myelitis with anti-myelin oligodendrocyte glycoprotein antibodies'],,,592873,,,,,,,G37.3,,
mondo:0035667,isolated optic neuritis without anti-MOG antibodies,['Isolated optic neuritis without anti-myelin oligodendrocyte glycoprotein antibodies'],,,592885,,,,,,,,,
mondo:0035668,isolated optic neuritis with anti-MOG antibodies,['Isolated optic neuritis with anti-myelin oligodendrocyte glycoprotein antibodies'],,,592888,,,,,,,,,
mondo:0035669,acute disseminated encephalomyelitis with anti-MOG antibodies,"['Acute disseminated encephalomyelitis with anti-myelin oligodendrocyte glycoprotein antibodies', 'ADEM with anti-MOG antibodies']",,,592894,,,,,,,G04.0,,
mondo:0035670,acute disseminated encephalomyelitis without anti-MOG antibodies,['Acute disseminated encephalomyelitis without anti-myelin oligodendrocyte glycoprotein antibodies'],,,592900,,,,,,,G04.0,,
mondo:0035678,Timothy syndrome type 1,"['TS1', 'LQT8 type 1']",,,595098,,,,,,,I49.8,,
mondo:0035679,Timothy syndrome type 2,"['TS2', 'LQT8 type 2']",,,595105,,,,,,,I49.8,,
mondo:0035682,fibrous dysplasia/McCune-Albright syndrome,"['FD/MAS spectrum', 'Fibrous dysplasia/McCune-Albright spectrum', 'FD/MAS syndrome']",,,595216,,,,,,,,,
mondo:0035684,epidermolysis bullosa simplex without extracutaneous involvement,['EBS without extracutaneous involvement'],,,595346,,,,,,,,,
mondo:0035685,epidermolysis bullosa simplex with extracutaneous involvement,['EBS with extracutaneous involvement'],,,595351,,,,,,,,,
mondo:0035689,syndrome of reduced sensitivity to thyroid hormone,,,,596426,,,,,,,,,
mondo:0035694,combined immunodeficiency due to RELA haploinsufficiency,['CID due to RELA haploinsufficiency'],,,596759,,,,,,,,,
mondo:0035696,incomplete septal cirrhosis,['Incomplete septal fibrosis'],,,596941,,,,,,,K74.6,,
mondo:0035706,SETD2-related microcephaly-severe intellectual disability-multiple congenital anomalies syndrome,,,,597743,,,,,,,,,
mondo:0035707,blepharophimosis-intellectual disability syndrome/genitopatellar overlap syndrome,,,,597746,,,,,,,,,
mondo:0035713,FOXG1 syndrome due to intragenic alteration,,,,598164,,,,,,,,,
mondo:0035734,hereditary angioedema with normal C1inh not related to F12 or PLG variant,,,,599418,,,,,,,,,
mondo:0035735,acquired hemophilia A,['AHA'],,,599480,C0272325,,C35345,,C536392,,,,
mondo:0035736,acquired hemophilia B,['AHB'],,,599485,,,,,,,,,
mondo:0035737,acquired factor V deficiency,,,,599490,,,C131624,,,,,,
mondo:0035738,acquired factor VII deficiency,,,,599495,,,C131625,,,,,,
mondo:0035740,acquired factor XI deficiency,['aFXI'],,,599507,,,C131627,,,,,,
mondo:0035742,factor V short isoforms-related bleeding disorder,['FV short isoforms-related bleeding disorder'],,,599519,,,,,,,,,
mondo:0035743,factor V amsterdam bleeding disorder,,,,599579,,,,,,,,,
mondo:0035759,factor V atlanta bleeding disorder,,,,600194,,,,,,,,,
mondo:0035763,idiopathic non-lupus full-house nephropathy,['Idiopathic non-lupus FHN'],,,567544,,,,,,,,,
mondo:0035764,idiopathic steroid-sensitive nephrotic syndrome with secondary steroid resistance,"['Idiopathic SSNS with secondary steroid resistance', 'Secondary steroid-resistant nephrotic syndrome', 'Secondary SRNS']",,,567546,,,,,,,,,
mondo:0035774,NRXN1-related severe neurodevelopmental disorder-motor stereotypies-chronic constipation-sleep-wake cycle disturbance,,,,600663,,,,,,,,,
mondo:0035775,CCNK-related neurodevelopmental disorder-severe intellectual disability-facial dysmorphism syndrome,,,,600668,,,,,,,,,
mondo:0035776,combined deficiency of factor VII and factor X,,,,600691,,,,,,,,,
mondo:0035777,parenteral nutrition-associated cholestasis,['PNAC'],,,567983,,,,,,,,,
mondo:0035782,"non-syndromic anorectal malformation with rectourethral fistula, bulbar type","['Non-syndromic ARM with rectourethral fistula, bulbar type', 'Non-syndromic anorectal malformation with rectobulbar fistula', 'Non-syndromic ARM with rectobulbar fistula']",,,600966,,,,,,,,,
mondo:0035783,"non-syndromic anorectal malformation with rectourethral fistula, prostatic type","['Non-syndromic anorectal malformation with rectoprostatic fistula', 'Non-syndromic ARM with rectourethral fistula, prostatic type', 'Non-syndromic ARM with rectoprostatic fistula']",,,600975,,,,,,,,,
mondo:0035819,cerebellar hypoplasia-intellectual disability-congenital microcephaly-dystonia-anemia-growth retardation syndrome,['CIMDAG syndrome'],,619273,603448,,,,,,,,,
mondo:0035821,isolated female hypospadias,,,,603515,,,,,,,,,
mondo:0035823,KLHL7-related Bohring-Opitz-like syndrome,['KLHL7-related BOS-like syndrome'],,,603689,,,,,,,,,
mondo:0035824,KLHL7-related cold-induced sweating-like syndrome,['KLHL7-related Crisponi-like syndrome'],,,603694,,,,,,,,,
mondo:0035826,symptomatic form of X-linked centronuclear myopathy in female carriers,"['Symptomatic form of XLMTM in female carriers', 'Symptomatic form of X-linked myotubular myopathy in female carriers', 'Symptomatic form of XLCNM in female carriers']",,,604680,,,,,,,,,
mondo:0035838,idiopathic multicentric Castleman disease,"['HHV-8-negative multicentric Castleman disease', 'Human herpesvirus-8-negative multicentric Castleman disease']",,,570431,,,,,,,,,
mondo:0035875,ivermectin toxicity,,,,574637,,,,,,,,,
mondo:0035876,belinostat toxicity or dose selection,,,,574671,,,,,,,,,
mondo:0035879,granuloma faciale,"['Granuloma of Lever', 'Facial granuloma of Lever']",,,615943,,,,,,,L92.2,,
mondo:0035882,chronic intervillositis of unknown etiology,['CIUE'],,,615970,,,,,,,,,
mondo:0035892,Mills syndrome,,,,94091,,,,,,,,,
mondo:0035930,neu-laxova syndrome due to 3-phosphoserine phosphatase deficiency,"['3-phosphoserine phosphatase deficiency, prenatal form']",,,583612,,,,,,,,,
mondo:0035940,B-lymphoblastic leukemia/lymphoma with t(9;22)(q34.1;q11.2),"['BCR-ABL1-like B-ALL', 'B-ALL with t(9;22)(q34.1;q11.2)', 'Philadelphia chromosome-like B-ALL']",0080643,,585909,,,C80331,,,,,,
mondo:0035941,B-lymphoblastic leukemia/lymphoma with t(v;11q23.3),"['B lymphoblastic leukemia lymphoma with t(v;11q23); MLL rearranged', 'B lymphoblastic leukaemia lymphoma with t(v;11q23); MLL rearranged', 'B Lymphoblastic Leukemia/Lymphoma with t(v;11q23.3); KMT2A Rearranged']",,,585918,,,C80332,,,,,,
mondo:0035942,B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1),"['B lymphoblastic leukemia lymphoma with t(12;21)(p13;q22); TEL-AML1', 'B-lymphoblastic leukemia/lymphoma with t(12;21)(p13.2;q22.1); ETV6-RUNX1', 'B lymphoblastic leukaemia lymphoma with t(12;21)(p13;q22); TEL-AML1']",,,585929,,,C80334,,,,,,
mondo:0035943,B-lymphoblastic leukemia/lymphoma with hyperdiploidy,,0080646,,585936,,,C80335,,,,,,
mondo:0035944,B-lymphoblastic leukemia/lymphoma with hypodiploidy,['Hypodiploid ALL'],0080647,,585942,,,C80338,,,,,,
mondo:0035945,B-lymphoblastic leukemia/lymphoma with t(5;14)(q31.1;q32.3),"['B lymphoblastic leukaemia lymphoma with t(5;14)(q31;q32); IL3-IGH', 'B lymphoblastic leukemia lymphoma with t(5;14)(q31;q32); IL3-IGH']",,,585948,,,C80340,,,,,,
mondo:0036025,toxicity to dolutegravir,,,,596744,,,,,,,,,
mondo:0036042,KAT6B-related multiple congenital anomalies syndrome,['KAT6B-related disorder'],,,597749,,,,,,,,,
mondo:0036045,euthyroid dysprealbuminemic hyperthyroxinemia,['Euthyroid dystransthyretinemic hyperthyroxinemia'],,,597939,,,,,,,,,
mondo:0036189,oculogastrointestinal-neurodevelopmental syndrome,['OGIN Syndrome'],,619318,611201,,,,,,,,,
mondo:0036192,EN1-related dorsoventral syndrome,"['ENDOVE syndrome', 'ENDOVES']",,,611223,,,,,,,,,
mondo:0036193,parkinsonism with polyneuropathy,,,619279,611237,,,,,,,,,
mondo:0036212,spastic paraparesis-cataracts-speech delay syndrome,['Fatty acyl-CoA reductase 1 superactivity'],,619338,615938,,,,,,,,,
mondo:0036217,lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to a point mutation,,,,615983,,,,,,,,,
mondo:0036218,lethal pontocerebellar hypoplasia-hypotonia-respiratory insufficiency syndrome due to biallelic deletions in the ATAD3 gene cluster,['Lethal 1p36.33 deletion syndrome'],,,615986,,,,,,,,,
mondo:0036482,retinitis pigmentosa 81,"['RP81', 'retinitis pigmentosa 81']",0080292,617871,,CN802781,,,,,,,,
mondo:0036483,short-rib thoracic dysplasia 18 with polydactyly,"['short-rib thoracic dysplasia 18 with polydactyly', 'SRTD18']",0080293,617866,,CN795020,,,,,,,,
mondo:0036484,"Charcot-Marie-Tooth disease, dominant intermediate G","['CMTDIG', 'Charcot-Marie-Tooth disease dominant intermediate G', 'Charcot-Marie-Tooth disease, dominant intermediate G']",0080294,617882,,CN847583,"['-0.01569', '0.0455', '-0.000267', '0.001102', '0.01034', '-0.03665', '-0.01343', '0.03903', '-0.02449', '-0.005024', '-0.010735', '-0.01278', '0.002743', '0.0088', '0.006092', '-0.01501', '0.001906', '-0.02469', '-0.00747', '-0.05765', '-0.0075', '-0.0179', '0.03003', '-0.0005', '0.01394', '-0.005886', '0.006313', '-0.003622', '-0.001471', '-0.0318', '0.02573', '-0.00965', '0.0361', '0.01883', '0.01544', '-0.02834', '-0.014336', '-0.01062', '0.001708', '-0.02596', '-0.007717', '-0.03204', '0.01353', '-0.01927', '-0.00235', '-0.03717', '-0.01677', '0.02036', '0.01513', '0.00872', '-0.001545', '-0.01103', '0.001657', '-0.00283', '-0.014046', '-0.03146', '0.02634', '-0.01075', '-0.03674', '0.009605', '0.01688', '-0.01028', '0.00815', '0.00827', '0.003044', '0.008675', '0.03836', '0.019', '-0.02747', '0.03079', '-0.02908', '0.00674', '0.005264', '-0.00907', '0.03476', '0.01302', '-0.002834', '0.008865', '-0.01025', '-0.03085', '-0.007385', '-0.003508', '-0.00989', '0.02155', '0.0001622', '-0.003626', '0.0146', '0.03152', '0.03696', '0.012794', '0.00885', '0.02505', '0.001397', '0.007805', '0.05902', '0.03143', '0.02509', '-0.037', '-0.012924', '0.012215']",,,,,,,
mondo:0036501,refractory malignant neoplasm,"['refractory malignant neoplasm', 'refractory cancer', 'clinical resistance', 'resistant cancer']",,,,C0677936,,C120186,,,,,,
mondo:0036511,childhood malignant kidney neoplasm,"['childhood malignant renal tumor', 'childhood malignant renal neoplasm', 'childhood kidney cancer', 'kidney cancer of childhood', 'paediatric kidney cancer', 'childhood malignant kidney tumour', 'pediatric kidney cancer', 'childhood malignant renal tumour', 'childhood malignant kidney tumor', 'childhood malignant kidney neoplasm']",,,,C4086162,,C123907,,,,,,
mondo:0036591,adrenal cortex neoplasm,"['adrenal cortex tumor', 'adrenal cortex tumour', 'adrenocortical tumor', 'adrenocortical neoplasm', 'neoplasm of adrenal cortex', 'adrenal cortex neoplasm', 'tumour of adrenal cortex', 'tumor of adrenal cortex', 'adrenocortical tumour']",,,,,,C2858,,D000306,,,,
mondo:0036595,ovarian Sertoli-Leydig cell tumor,"['Sertoli-Leydig cell tumor of the ovary', 'Sertoli-Leydig neoplasm of the ovary', 'Sertoli-Leydig cell tumour of ovary', 'Sertoli-Leydig cell tumor of ovary', 'arrhenoblastoma', 'androblastoma', 'ovarian Sertoli-Leydig cell tumor', 'Sertoli-Leydig cell tumour of the ovary', 'Sertoli-Leydig neoplasm of ovary', 'ovarian Sertoli-Leydig cell neoplasm']",,,,C0003810,,C2880,1000429,,,,,
mondo:0036688,rhabdomyoma,"['rhabdomyoma, benign', 'rhabdomyoma', 'Rhabdomyomatous neoplasm']",,,,C0035411,,C3358,,D012207,,,,
mondo:0036696,spleen neoplasm,"['tumor of spleen', 'neoplasm of spleen', 'spleen tumour', 'splenic neoplasm', 'tumour of spleen', 'spleen tumor']",,,,,,C3383,,,,,,
mondo:0036779,axillary neoplasm,"['axilla tumor', 'tumour of axilla', 'axilla tumour', 'tumor of axilla', 'axillary neoplasm', 'neoplasm of axilla']",,,,C1290308,,C35749,,,,,,
mondo:0036781,benign axillary neoplasm,"['axillary neoplasm, benign', 'benign axillary neoplasm']",,,,C0684828,,C35750,,,,,,
mondo:0036870,lymphatic vessel neoplasm,"['neoplasm of lymphatic vessel', 'tumor of the lymph vessel', 'neoplasm of the lymphatic vessel', 'lymphatic vessel neoplasm', 'lymph vessel neoplasm', 'lymph vessel tumor', 'neoplasm of the lymph vessel', 'tumour of the lymphatic vessel', 'tumour of lymphatic vessel', 'lymphatic vessel tumour', 'neoplasm of lymph vessel', 'tumor of lymph vessel', 'lymphatic vessel tumor', 'tumor of the lymphatic vessel', 'lymph vessel tumour', 'tumour of lymph vessel', 'tumour of the lymph vessel', 'tumor of lymphatic vessel']",,,,C0206619,,C3723,,,,,,
mondo:0036915,benign ovarian mucinous tumor,"['ovarian mucinous neoplasm, benign', 'benign ovarian mucinous tumor', 'benign ovarian mucinous neoplasm']",,,,C1511100,,C40039,1000115,,,,,
mondo:0036918,punctate acrokeratoderma freckle-like pigmentation,,,,99710,,,,,,,,,
mondo:0036976,benign epithelial neoplasm,"['benign tumor of epithelium', 'benign tumor of the epithelium', 'epithelioma, benign', 'benign tumour of epithelium', 'benign epithelial tumor', 'benign tumour of the epithelium', 'benign epithelial tumour', 'benign epithelial neoplasm', 'benign epithelioma', 'benign neoplasm of the epithelium', 'epithelial neoplasm, benign', 'benign neoplasm of epithelium']",,,,C0334232,,C4092,,,,,,
mondo:0036990,benign Leydig cell tumor,"['Leydig cell tumor, benign', 'benign Leydig cell neoplasm', 'benign interstitial cell neoplasm', 'benign Leydig cell tumor', 'benign interstitial cell tumour', 'adenoma, interstitial', 'benign interstitial cell tumor']",,,,C0334409,,C4212,,,,,,
mondo:0037002,benign phyllodes tumor,"['benign phyllodes tumor', 'phyllodes tumor, benign', 'benign cystosarcoma phyllodes', 'benign phyllodes neoplasm']",,,,,,C4274,,,,,,
mondo:0037003,malignant phyllodes tumor,"['malignant phyllodes neoplasm', 'malignant cystosarcoma phyllodes', 'malignant phyllodes tumor', 'phyllodes tumor, malignant']",,,,,,C4275,,,,,,
mondo:0037105,lung germ cell tumor,"['lung germ cell neoplasm', 'lung germ cell tumor']",,,,C1708771,,C45636,,,,,,
mondo:0037149,"HSD10 disease, atypical type","['Syndromic X-linked intellectual disability type 10', 'HSD10 deficiency, atypical type', 'X-linked intellectual disability-choreoathetosis-abnormal behaviour syndrome', 'X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome']",,,85295,,,,,,,,,
mondo:0037250,childhood testicular neoplasm,"['paediatric testicular neoplasm', 'pediatric neoplasm of testis', 'paediatric neoplasm of testis', 'pediatric neoplasm of the testis', 'paediatric neoplasm of the testis', 'testicular tumor, childhood', 'pediatric testicular neoplasm', 'childhood neoplasm of testis', 'childhood testicular neoplasm', 'childhood neoplasm of the testis', 'neoplasm of testis of childhood']",,,,,,C5053,,,,,,
mondo:0037251,congestive splenomegaly,,,,,,,,,,,,,
mondo:0037252,thecoma,['thecoma'],,,,,,C3405,,D013798,,,,
mondo:0037253,ovarian thecoma,"['ovarian theca cell tumour', 'theca cell tumor of the ovary', 'theca cell tumor of ovary', 'theca cell tumour of the ovary', 'theca cell tumour of ovary', 'thecoma of ovary', 'ovarian thecoma', 'ovarian theca cell tumor', 'theca cell neoplasm of ovary', 'ovarian theca cell neoplasm', 'ovary thecoma', 'thecoma of the ovary', 'theca cell neoplasm of the ovary']",,,,,,C66989,,,,,,
mondo:0037254,transitional cell neoplasm,"['transitional cell tumor', 'transitional cell neoplasm', 'transitional cell tumour']",,,,C0334265,,C6783,,,,,,
mondo:0037255,ovarian serous tumor,"['ovarian serous neoplasm', 'serous tumor of ovary', 'serous tumour of the ovary', 'serous neoplasm of ovary', 'ovarian serous tumor', 'serous neoplasm of the ovary', 'serous tumour of ovary', 'serous tumor of the ovary']",,,,C0476122,,C8431,,,,,,
mondo:0037256,serous neoplasm,['serous neoplasm'],,,,C1335951,,C7074,,,,,,
mondo:0037398,pneumonia caused by pseudomonas aeruginosa infection,,,,90066,,,,,,,,,
mondo:0037735,sebaceous gland cancer,"['malignant tumour of sebaceous gland', 'malignant tumor of the sebaceous gland', 'malignant neoplasm of sebaceous gland', 'malignant neoplasm of the sebaceous gland', 'malignant sebaceous neoplasm', 'malignant sebaceous tumour', 'malignant tumor of sebaceous gland', 'malignant sebaceous gland neoplasm', 'malignant sebaceous tumor', 'malignant sebaceous gland tumour', 'cancer of sebaceous gland', 'malignant sebaceous gland tumor', 'malignant tumour of the sebaceous gland']",,,,C1382026,,C8409,,,,,,
mondo:0037736,infratentorial neoplasm,"['infratentorial tumour', 'infratentorial tumor', 'infratentorial tumors', 'infratentorial neoplasm', 'infratentorial tumours', 'neoplasms, infratentorial', 'brain neoplasms, infratentorial', 'infratentorial neoplasms']",,,,,,C3139,,,,,,
mondo:0037737,peritoneal solitary fibrous tumor,['peritoneal solitary fibrous tumor'],,,,C4288403,,C126357,,,,,,
mondo:0037738,cauda equina cancer,"['malignant cauda equina neoplasm', 'malignant neoplasm of cauda equina', 'cancer of cauda equina']",,,,C0349017,,,,,,,,
mondo:0037739,benign neoplasm of cauda equina,,,,,C0686404,,,,,,,,
mondo:0037740,"malignant central nervous system mesenchymal, non-meningothelial neoplasm","['malignant soft tissue neoplasm of central nervous system', 'malignant central nervous system soft tissue neoplasm', 'malignant CNS soft tissue tumor', 'malignant soft tissue tumor of CNS', 'malignant soft tissue neoplasm of CNS', 'malignant central nervous system mesenchymal, non-meningothelial neoplasm', 'malignant soft tissue tumor of central nervous system', 'malignant soft tissue tumor of the CNS', 'malignant central nervous system mesenchymal non-meningothelial tumour', 'malignant central nervous system mesenchymal, non-meningothelial tumour', 'malignant soft tissue tumour of the CNS', 'malignant central nervous system soft tissue tumour', 'malignant CNS soft tissue neoplasm', 'soft tissue cancer of central nervous system', 'malignant central nervous system soft tissue tumor', 'central nervous system mesenchymal non-meningothelial tumor, malignant', 'soft tissue cancer of the central nervous system', 'malignant soft tissue neoplasm of the central nervous system', 'malignant soft tissue neoplasm of the CNS', 'malignant soft tissue tumour of the central nervous system', 'malignant CNS soft tissue tumour', 'malignant central nervous system mesenchymal, non-meningothelial tumor', 'malignant soft tissue tumor of the central nervous system', 'malignant soft tissue tumour of central nervous system', 'malignant soft tissue tumour of CNS']",,,,C1334571,,C6758,,,,,,
mondo:0037742,endometrioid stromal and related neoplasms,"['endometrioid stromal and related tumors', 'endometrioid stromal and related neoplasms', 'endometrioid stromal and related tumours']",,,,C4287868,,C8384,,,,,,
mondo:0037743,mediastinal soft tissue cancer,"['malignant mediastinal soft tissue neoplasm', 'malignant soft tissue tumour of the mediastinum', 'mediastinal mesenchymal tumor, malignant', 'malignant mediastinal soft tissue tumor', 'malignant mediastinal soft tissue tumour', 'malignant soft tissue neoplasm of the mediastinum', 'malignant soft tissue tumor of mediastinum', 'malignant soft tissue tumor of the mediastinum', 'malignant soft tissue tumour of mediastinum', 'malignant mediastinal mesenchymal tumour', 'malignant soft tissue neoplasm of mediastinum']",,,,C1334599,,C6642,,,,,,
mondo:0037744,neoplasm of retromolar area,['tumour of retromolar area'],,,,C0345590,,,,,,,,
mondo:0037745,fibromyxoid tumor,"['fibromyxoid neoplasm', 'fibromyxoid tumor', 'fibromyxoma', 'fibromyxoma, benign']",,,,,,C66760,,,,,,
mondo:0037746,malignant vaginal mixed epithelial and mesenchymal neoplasm,"['malignant vaginal mixed epithelial and mesenchymal neoplasm', 'malignant vaginal mixed epithelial and mesenchymal tumor', 'malignant vaginal mixed epithelial and mesenchymal tumour']",,,,C1512974,,C40276,,,,,,
mondo:0037747,spinal injury,['vertebral column injury'],,,,,,,,D013124,,,,
mondo:0037748,hyperlipoproteinemia,['hyperlipoproteinemia'],,,,C0020476,,C34709,,D006951,,,,0010980
mondo:0037792,carbohydrate metabolism disease,"['carbohydrate metabolic process disease', 'disorder of carbohydrate metabolic process']",,,,,,,,,,,,
mondo:0037807,glycerol metabolism disease,"['glycerol metabolic process disease', 'disorder of glycerol metabolic process']",,,,C0342762,,,,,,,,
mondo:0037821,porphyrin metabolism disease,"['porphyrin-containing compound metabolic process disease', 'disorder of porphyrin-containing compound metabolic process']",,,,,,,,,,,,
mondo:0037829,purine metabolism disease,"['disorder of purine nucleobase metabolic process', 'purine nucleobase metabolic process disease']",,,,C0268104,,,,,,,,
mondo:0037847,vertebral joint disorder,"['disorder of intervertebral joint', 'disease of intervertebral joint', 'intervertebral joint disease or disorder', 'intervertebral joint disease']",,,,,,,,,,,,
mondo:0037858,inherited fatty acid metabolism disorder,['fatty acid metabolism disorder'],,,,,,C117115,,,,,,
mondo:0037870,valine metabolism disease,"['valine metabolic process disease', 'disorder of valine metabolic process']",,,,C2919304,,,,,,,,
mondo:0037871,amino acid metabolism disease,"['cellular amino acid metabolic process disease', 'disorder of cellular amino acid metabolic process', 'amino acid metabolism disorder']",,,,,,C97090,,,,,,
mondo:0037872,bordetellosis,"['Bordetella Infection', 'INFECT BORDETELLA', 'Infections, Bordetella', 'Bordetella Infections', 'Bordetellosis', 'Bordetella caused disease or disorder', 'Infection, Bordetella', 'Bordetella infection']",,,,C0006015,,,1001275,D001885,041.85,,,
mondo:0037937,pyrimidine metabolism disease,"['disorder of pyrimidine nucleobase metabolic process', 'pyrimidine nucleobase metabolic process disease']",,,,C0268127,,,,,,,,
mondo:0037938,inborn disorder of aspartate family metabolism,"['inborn error of aspartate family amino acid metabolic process', 'rare inborn error of aspartate family amino acid metabolic process']",,,,,,,,,,,,
mondo:0037939,porphyria,,,,,,,,,,,,,
mondo:0037940,inherited auditory system disease,['hereditary auditory system disease'],,,,C1285174,,,,,,,,
mondo:0038268,autoimmune neurological channelopathy,,,,98750,,,,,,,,,
mondo:0040500,glycosylphosphatidylinositol biosynthesis defect 16,"['GPIBD16', 'mental retardation, autosomal recessive 62', 'intellectual disability, autosomal recessive 62', 'glycosylphosphatidylinositol biosynthesis defect 16']",0081223,617816,,,"['-0.0749', '0.0512', '0.005623', '-0.03123', '0.0482', '-0.07526', '0.00759', '0.05173', '-0.05774', '-0.04498', '-0.01561', '0.0083', '0.01599', '0.007126', '-0.01743', '-0.02058', '-0.0002975', '-0.0293', '-0.04236', '-0.11444', '-0.01671', '-0.02249', '0.04965', '-0.02383', '0.01964', '-0.007008', '-0.010605', '-0.00667', '0.01443', '-0.0365', '0.03897', '0.0172', '0.0731', '0.02634', '0.00115', '-0.03345', '0.01522', '-0.01817', '-0.002459', '-0.0619', '0.02728', '-0.05936', '0.02516', '-0.02487', '-0.01516', '-0.0527', '0.0008745', '0.02803', '0.012375', '0.0264', '-0.01863', '-0.02429', '-0.011734', '0.00937', '-0.03824', '-0.03387', '0.0736', '-0.02425', '-0.05692', '0.00635', '0.04266', '0.0321', '0.03017', '0.00877', '0.001179', '-0.00706', '0.08527', '0.04578', '-0.05447', '0.03824', '-0.05273', '0.02159', '0.0158', '-0.01563', '0.02876', '0.05786', '0.00782', '-0.00898', '-0.05026', '-0.04086', '-0.003113', '0.01035', '0.00431', '0.03302', '0.005238', '0.002377', '0.02519', '0.06476', '0.0645', '0.000574', '0.03876', '0.04694', '-0.001694', '-0.006508', '0.1415', '0.03714', '0.07166', '-0.0958', '0.0065', '0.02028']",,,,,,,
mondo:0040501,"ehlers-danlos syndrome, arthrochalasia type, 2","['EDS 7B', 'EDSARTH2', 'Ehlers-Danlos syndrome, arthrochalasia type, 2', 'Ehlers-Danlos syndrome, type VIIb, Autosomal dominant']",0080728,617821,,,,,,,,,,
mondo:0040502,glucocorticoid deficiency 5,"['GCCD5', 'glucocorticoid deficiency 5']",,617825,,,,,,,,,,
mondo:0040503,blepharocheilodontic syndrome 2,"['BCDS2', 'BLEPHAROCHEILODONTIC syndrome 2', 'CTNND1 blepharo-cheilo-odontic syndrome']",0080346,617681,,C4540127,,,,,,,,
mondo:0040566,inherited glutathione metabolism disease,"['rare inborn error of glutathione metabolic process', 'disorder of glutathione metabolism', 'inborn error of glutathione metabolic process']",,,,C0268518,,,,,,,,
mondo:0040653,autosomal recessive ocular albinism,"['AROA', 'ocular albinism (disease), autosomal recessive']",,,,,,,,,,,,
mondo:0040654,autosomal dominant oculocutaneous albinism,"['oculocutaneous albinism, autosomal dominant']",,,,,,,,,,,,
mondo:0040671,class V glucose-6-phosphate dehydrogenase deficiency,"['favism', 'G6PD deficiency', 'G6PD class V variant anaemia', 'glucose-6-phosphate dehydrogenase deficiency class V variant anaemia']",,,362,C0272060,,,,,,,,
mondo:0040673,malignant peritoneal germ cell tumor,['malignant peritoneal germ cell tumor'],,,,C4526657,,C136410,,,,,,
mondo:0040674,orgasm disorder,,,,,,,,,,,F52.3,,
mondo:0040675,myofibroblastoma,['myofibroblastoma'],,,,,,C49012,,,,,,
mondo:0040676,great vessel cancer,"['malignant great vessel tumor', 'malignant great vessel of heart neoplasm', 'great vessel cancer', 'malignant neoplasm of great vessel of heart', 'cancer of great vessel of heart', 'malignant great vessel tumour', 'malignant great vessel neoplasm']",,,,C3665405,,C4575,,,,,,
mondo:0040677,invasive carcinoma,['invasive carcinoma'],,,,C1334274,,C9480,,,,,,
mondo:0040678,infiltrating urothelial carcinoma,"['infiltrating urothelial carcinoma', 'infiltrating transitional cell carcinoma of the urinary tract']",,,,C1512751,,C39853,,,,,,
mondo:0040679,urothelial carcinoma,"['transitional cell car. -uroth.', 'urothelial carcinoma', 'Uroepithelial carcinoma', 'transitional cell carcinoma of the urothelial tract', 'transitional cell carcinoma of the urinary tract']",,,,C2145472,,C4030,0008528,,,,,
mondo:0040698,subacute bursitis,,,,,C1290159,,,,,,,,
mondo:0040699,necrotizing scleritis,,,,,,,,,,379.09,,,
mondo:0040700,orbital dermoid cyst,"['dermoid cyst of the orbit', 'orbit dermoid cyst', 'epidermal dermoid cyst', 'dermoid cyst of orbit']",,,,C0346356,,C4548,,,,,,
mondo:0040728,Campylobacter fetus infectious disease,"['infection by Campylobacter foetus', 'infection by vibrio foetus', 'infection caused by Campylobacter foetus', 'infection caused by vibrio foetus']",,,,C0275979,,,,,,,,
mondo:0040732,Pseudomonas aeruginosa infectious disease,,,,,C0276075,,,,,,,,
mondo:0040753,latent tuberculosis infection,"['inactive TB', 'inactive tuberculosis', 'LTBI']",,,,C1609538,,,,D055985,,,,
mondo:0040870,primary polydipsia,,,,,,,,,,,,,
mondo:0040871,psychogenic polydipsia,,,,,,,,,,,,,
mondo:0040872,non-psychogenic polydipsia,,,,,,,,,,,,,
mondo:0040922,latent early syphilis,,,,,C0275842,,,,,,,,
mondo:0040923,late latent syphilis,,,,,C1260915,,C128371,,,,,,
mondo:0040925,latent yaws,,,,,C0153240,,,,,,,,
mondo:0040998,Pasteurella multocida infectious disease,,,,,C1260911,,,,,,,,
mondo:0041052,postherpetic neuralgia,,,,466673,C0032768,,,,,,,,
mondo:0041086,mixed anxiety and depressive disorder,,,,,,,,,,,,,
mondo:0041093,central retinal vein occlusion with macular edema,,,,,,,,,,,,,
mondo:0041095,malignant otitis externa caused by Pseudomonas aeruginosa,['Pseudomonas aeruginosa caused malignant otitis externa'],,,,C0395818,,,,,,,,
mondo:0041114,peripheral ischemia,['peripheral ischaemic vascular disease'],,,,,,,,,,,,
mondo:0041154,disorder of neck of urinary bladder,,,,,,,,,,,,,
mondo:0041167,carcinoid crisis,,,,,C0342569,,,,,,,,
mondo:0041182,polymorphic light eruption,,,,,C0031736,,,,,,,,
mondo:0041186,Rowell syndrome,,,,,C0406637,,,,,,,,
mondo:0041259,diphtheritic myocarditis,['Corynebacterium diphtheriae caused myocarditis'],,,,C0152952,,,,,,,,
mondo:0041261,disorder of acid-base balance,,,,,C0268029,,,,,,,,
mondo:0041284,primary motor cortex epilepsy,"['epilepsy of primary motor cortex', 'primary motor cortex epilepsy']",,,,C0234978,,,,,,,,
mondo:0041295,acute papillary necrosis,"['kidney papillary necrosis, acute', 'acute kidney papillary necrosis']",,,,,,,,,,,,
mondo:0041366,acute epiglottitis,"['epiglottitis, acute']",,,,,,,,,,,,
mondo:0041403,toxic amblyopia,['nutritional optic neuropathy'],,,,,,,,,,,,
mondo:0041447,metastatic malignant neoplasm in the colon,"['metastatic malignant neoplasm in the colon', 'metastatic malignant neoplasm to the colon', 'metastatic neoplasm to the colon', 'metastatic tumour to the colon', 'metastatic tumor to the colon']",,,,C0346974,,C8411,,,,,,
mondo:0041448,metastasis from malignant tumor of colon,,,,,C1282500,,,,,,,,
mondo:0041526,pregnancy disorder with abortive outcome,,,,,,,,,,,O00-O08,,
mondo:0041535,mesenteric lymphadenitis due to Yersinia infection,['Yersinia pseudotuberculosis caused mesenteric lymphadenitis'],,,,C0275758,,,,,,,,
mondo:0041536,Far-East scarlet-like fever,"['Izumi fever', 'FESLF']",,,,C0277513,,,,,,,,
mondo:0041656,ST-elevation myocardial infarction,['STEMI'],,,,,,,0008585,D000072657,,,,
mondo:0041751,multibacillary leprosy,['lepromatous leprosy'],,,,,,,,D056006,,,,
mondo:0041752,paucibacillary leprosy,['tuberculoid leprosy'],,,,,,,,D056005,,,,
mondo:0041755,twin reversal arterial perfusion syndrome,,,,,C1562817,,,,,,,,
mondo:0041775,intraoperative floppy iris syndrome,,,,,C1688637,,,,,,,,
mondo:0041806,drug-resistant tuberculosis,,,,,,,,,,,,,
mondo:0041825,bacterial meningitis caused by gram-negative bacteria,['meningitis with gramme negative bacteria'],,,,C0854215,,,,,,,,
mondo:0041850,pneumonia caused by gram negative bacteria,"['pneumonia due to gramme negative bacteria', 'gramme negative pneumonia']",,,,C0854248,,,,,,,,
mondo:0041879,staphylococcus aureus pneumonia,['Staphylococcus aureus caused pneumonia'],,,,,,,,,,,,
mondo:0041903,gonococcal infection of joint,,,,,C0153216,,,,,,,,
mondo:0041959,fibrosis of bile duct,,,,,C0520571,,,,,,,,
mondo:0041996,thallium poisoning,,,,,,,,,,,,,
mondo:0042233,disseminated candidiasis,['systemic candida infections'],,,,,,C116812,,,,,,
mondo:0042370,Yersinia enterocolitica infectious disease,,,,,,,,,,,,,
mondo:0042433,mycotic endocarditis,['Fungi caused endocarditis (disease)'],,,,C0276648,,,,,,,,
mondo:0042451,endomyometritis,,,,,,,,,,,,,
mondo:0042452,tertiary lesion of yaws,,,,,C0343833,,,,,,,,
mondo:0042458,Trichinella spiralis infectious disease,['Trichinella spiralis caused disease or disorder'],,,,C3887668,,,,,,,,
mondo:0042484,disseminated sporotrichosis,,,,,C0276725,,,,,,,,
mondo:0042485,infective arthritis,"['septic arthritis', 'infective arthritis']",,,,,,C26700,,,,,,
mondo:0042486,"polyposis syndrome, hereditary mixed, 1","['colorectal adenoma and carcinoma 1', 'polyposis syndrome, hereditary mixed, 1', 'HMPS1', 'polyposis syndrome, hereditary mixed 1', 'colorectal cancer, susceptibility to, 4', 'colorectal cancer, susceptibility to, on chromosome 15', 'chromosome 15Q13-q14 Duplication syndrome, 40-Kb']",0111685,601228,,,,,,,,,,
mondo:0042487,uterine cervix carcinoma in situ,"['cervical carcinoma in situ aJCC v6', 'cervix uteri intraepithelial neoplasia grade 3 aJCC v6', 'CIN grade 3 aJCC v6', 'FIGO stage 0 cervix carcinoma', 'carcinoma in situ of the cervix uteri aJCC v6', 'carcinoma in situ of cervix uteri aJCC v6', 'FIGO stage 0 carcinoma of the cervix', 'cervical intraepithelial neoplasia grade III with severe dysplasia', 'carcinoma in situ of cervix', 'cervix Severe dysplasia aJCC v6', 'severe dysplasia of the cervix uteri aJCC v6', 'squamous intraepithelial neoplasia, grade III', 'stage 0 cervical cancer', 'stage 0 uterine cervix carcinoma', 'FIGO stage 0 uterine cervix carcinoma', 'cervical cancer stage 0 aJCC v6', 'intraepithelial neoplasia of uterine cervix grade 3 aJCC v6', 'severe dysplasia of cervix uteri aJCC v6', 'carcinoma of cervix stage 0', 'FIGO stage 0 carcinoma of the uterine cervix', 'cervix Ca in situ', 'severe cervical dysplasia aJCC v6', 'grade 3 cervical intraepithelial neoplasia aJCC v6', 'severe dysplasia of cervix aJCC v6', 'carcinoma in situ of cervix aJCC v6', 'CIN III - carcinoma in situ of cervix', 'intraepithelial neoplasia of the cervix uteri grade 3 aJCC v6', 'uterine cervix intraepithelial neoplasia grade 3 aJCC v6', 'carcinoma in situ of the uterine cervix aJCC v6', 'cervix uteri carcinoma in situ', 'FIGO stage 0 carcinoma of cervix', 'severe dysplasia of the cervix aJCC v6', 'FIGO stage 0 cervical carcinoma', 'CIN 3 aJCC v6', 'uterine cervix Severe dysplasia aJCC v6', 'cervical Severe dysplasia aJCC v6', 'cervix uteri Severe dysplasia aJCC v6', 'severe dysplasia of uterine cervix aJCC v6', 'cervical intraepithelial neoplasia grade 3 aJCC v6', 'intraepithelial neoplasia of the cervix grade 3 aJCC v6', 'CIN III - severe dyskaryosis', 'carcinoma in situ of uterine cervix', 'FIGO stage 0 carcinoma of uterine cervix', 'intraepithelial neoplasia of the uterine cervix grade 3 aJCC v6', 'carcinoma in situ of uterine cervix aJCC v6', 'uterine cervix carcinoma in situ aJCC v6', 'cervix intraepithelial neoplasia grade 3 aJCC v6', 'severe dysplasia of cervix', 'FIGO stage 0 carcinoma of cervix uteri', 'CIN III', 'severe dysplasia of the uterine cervix aJCC v6', 'intraepithelial neoplasia of cervix grade 3 aJCC v6', 'cervix uteri carcinoma in situ aJCC v6', 'FIGO stage 0 carcinoma of the cervix uteri', 'FIGO stage 0 cervix uteri carcinoma', 'intraepithelial neoplasia of cervix uteri grade 3 aJCC v6', 'stage 0 cervical cancer aJCC v6', 'carcinoma in situ of the cervix aJCC v6', 'cervix carcinoma in situ aJCC v6']",8991,,,C0851140,,C4000,,D018290,233.1,,,
mondo:0042488,Cestode infectious disease,"['Bertielliases', 'Coenuriasis', 'Dipylidiasis', 'Raillietiniasis', 'Cenuriases', 'tapeworm infection', 'infection, cestode', 'infections, tapeworm', 'infection, tapeworm', 'Cestoda caused disease or disorder', 'infections, cestode', 'cestode infection', 'Bertielliasis', 'Cenuriasis', 'Raillietiniases', 'Dipylidiases', 'Coenuriases', 'tapeworm infections']",,,,,,,1001287,D002590,123.9,,,
mondo:0042489,disease susceptibility,"['susceptibilities, disease', 'disease susceptibilities', 'diatheses', 'diathesis', 'susceptibility, disease']",,,,,,,,D004198,,,,
mondo:0042490,"neutropenia, severe congenital, 1, autosomal dominant","['neutropenia, severe congenital 1, autosomal dominant', 'neutropenia, severe congenital, 1, autosomal dominant', 'SCN1']",0080625,202700,,,,,,C565969,,,,
mondo:0042491,cervical squamous intraepithelial neoplasia,"['squamous intraepithelial lesion of cervix uteri', 'cervical sil', 'squamous intraepithelial lesion of the cervix', 'uterine cervix squamous intraepithelial lesion', 'CIN', 'cervix squamous intraepithelial lesion', 'squamous intraepithelial lesion of cervix', 'cervical squamous intraepithelial neoplasia', 'cervical squamous intraepithelial lesion', 'squamous intraepithelial lesion of the cervix uteri', 'squamous intraepithelial lesion of uterine cervix', 'cervix uteri squamous intraepithelial lesion', 'uterine cervix sil', 'cervix uteri sil', 'squamous intraepithelial lesion of the uterine cervix']",,,,,,C7346,,D065310,,,,
mondo:0042493,gastric non-hodgkin lymphoma,"['gastric non-Hodgkin^s lymphoma', 'non-Hodgkin^s lymphoma of stomach', 'non-Hodgkin lymphoma of stomach', 'primary gastric non-Hodgkin^s lymphoma', 'stomach lymphoma, non-Hodgkins type', 'non-Hodgkins gastric lymphoma', 'gastric non-Hodgkin lymphoma', 'non-Hodgkin^s lymphoma of the stomach', 'stomach non-Hodgkin lymphoma', 'lymphoma, gastric non Hodgkins type']",,,,C1333784,,C27235,,,,,,
mondo:0042494,childhood malignant melanoma,"['melanoma (disease) of childhood', 'paediatric melanoma (disease)', 'malignant melanoma, childhood', 'childhood melanoma', 'pediatric melanoma (disease)']",,,,C4329660,,C131506,,,,,,
mondo:0042495,arteriosclerotic retinopathy,"['arteriosclerosis, retina', 'retinopathy, arteriosclerotic', 'retina arteriosclerosis disorder', 'arteriosclerosis disorder of retina']",,,,C0339478,,,,,440.8,,,
mondo:0042496,ergotism,"['poisonings, ergot', 'Saint Anthonys fire', 'ergot poisoning', 'Saint Anthony fire', 'St. Anthony fire', 'Saint Anthony^s fire', 'ergot poisonings', 'St. Anthony^s fire', 'St Anthony^s fire', 'fire, St. Anthonys', 'ergotisms', 'poisoning, ergot', 'St. Anthonys fire', 'ergotism']",,,,,,,,D004881,988.2,,,
mondo:0042497,mycotoxicosis,"['fungus poisoning', 'fungus Poisonings', 'Fungi caused poisoning', 'Mycotoxicoses', 'poisoning, fungus', 'Poisonings, fungus']",,,,,,,,D015651,,,,
mondo:0042498,Ruzicka-Goerz-Anton syndrome,"['ichthyosis congenita, neurosensory deafness, oligophrenia, dental aplasia, brachydactyly, clinodactyly, accessory cervical ribs and thyroid carcinoma', 'Ruzicka Goerz Anton syndrome', 'ichthyosis deafness intellectual disability skeletal anomalies', 'ichthyosis deafness mental retardation skeletal anomalies']",,,,C2931438,,,,C537192,,,,
mondo:0042499,benign familial neonatal-infantile seizures 1,"['BFIC1', 'convulsions, benign familial infantile, 1', 'benign familial infantile convulsions syndrome', 'seizures, benign familial infantile, 1', 'BFIS1', 'benign infantile familial convulsions']",0081114,601764,,,,,,,,,,
mondo:0042600,Sammartino-Decreccio syndrome,"['superficial annular corneal dystrophy, ichthyosis nigrans, microcephaly and mild mental subnormality', 'Sammartino Decreccio syndrome']",,,,,,,,,,,,
mondo:0042601,Samson-Gardner syndrome,"['Samson Gardner syndrome', 'craniosynostosis, microcephaly, hydrancephaly, humero-radial synostosis, and thumb aplasia']",,,,C2931448,,,,C537230,,,,
mondo:0042602,Samson-Viljoen syndrome,"['lateral facial cleft, cleft lip and palate, anophthalmia, microtia, clavicular agenesis and asternia', 'Samson Viljoen syndrome']",,,,C2931449,,,,C537231,,,,
mondo:0042603,Sanderson-Fraser syndrome,"['proptosis, Robin association, clenched hands, and multiple abnormalities', 'Sanderson Fraser syndrome']",,,,C2931450,,,,C537232,,,,
mondo:0042604,Sandhaus-Ben-Ami syndrome,"['Sandhaus Ben-Ami syndrome', 'patella hypoplasia skeletal malformations']",,,,C2931451,,,,C537233,,,,
mondo:0042605,Y chromosome infertility due to DAZ1 deletion,"['Y chromosome infertility', 'male sterility due to Y-chromosome deletions', 'Y chromosome microdeletions', 'deleted in azoospermia', 'DAZ']",,,,,,,,,,,,
mondo:0042705,prostatic malacoplakia associated with prostatic abscess,['prostatic malacoplakia with prostatic and seminal vesicle abscess'],,,,C2931457,,,,C537244,,,,
mondo:0042717,Saul-Wilkes-Stevenson syndrome,['Saul Wilkes Stevenson syndrome'],,,,C2931266,,,,C536617,,,,
mondo:0042724,"macrocephaly, intellectual disability, short stature, spastic paraplegia and cns malformations",['Volcke Soekarman syndrome'],,,,,,,,,,,,
mondo:0042726,"macrogyria, pseudobulbar palsy and intellectual disability",['Kuzniecky Andermann syndrome'],,,,C2931598,,,,C537722,,,,
mondo:0042727,sacrococcygeal teratoma,"['presacral teratoma', 'pre-sacral teratoma', 'sacrococcygeal teratoma']",,,494421,C0559459,,C99055,,,,,,0030736
mondo:0042902,Say-Carpenter syndrome,"['metaphyseal dysplasia hypertelorism hypospadias', 'Say Carpenter syndrome']",,,,,,,,,,,,
mondo:0042911,Schwartz-Cohen-addad-Lambert syndrome,"['congenital melanocytosis with myelomeningocele and hydrocephalus', 'Schwartz Cohen-Addad Lambert syndrome']",,,,C2931036,,,,C535835,,,,
mondo:0042912,Schlegelberger-Grote syndrome,"['syndrome with triphalangia of thumbs, thrombasthenia Glanzmann and deafness of internal ear', 'triphalangeal thumbs thrombocytopathy deafness', 'Schlegelberger Grote syndrome']",,,,C2931273,,,,C536635,,,,
mondo:0042913,Schrander-stumpel-Theunissen-Hulsmans syndrome,"['vitiligo, psychomotor retardation, cleft palate and facial dysmorphism', 'Schrander-Stumpel Theunissen Hulsmans syndrome', 'vitiligo vulgaris, cleft palate, somatic and psychomotor retardation and facial dysmorphism']",,,,C2931275,,,,C536639,,,,
mondo:0042924,Vagneur-Triolle-Ripert syndrome,"['Vagneur Triolle Ripert syndrome', 'hypertelorism, short midface, arachnodactyly, coloboma of iris and delayed bone age']",,,,,,,,,,,,
mondo:0042956,Saal-Bulas syndrome,"['Saal Bulas syndrome', 'ectrodactyly, diaphragmatic hernia, congenital heart defect, and agenesis of the corpus callosum']",,,,C2931439,,,,C537193,,,,
mondo:0042960,Sackey-Sakati-Aur syndrome,"['multiple dysmorphic features and pancytopenia', 'Aur syndrome', 'Sackey Sakati Aur syndrome', 'pancytopenia multiple congenital anomalies']",,,,C2931442,,,,C537219,,,,
mondo:0042961,sacral hemangiomas multiple congenital abnormalities,,,,,C2931443,,,,C537222,,,,
mondo:0042962,Slti-Salem syndrome,"['hypogonadotropic hypogonadism alopecia', 'hypogonadism and frontoparietal alopecia', 'Slti Salem syndrome']",,,,C2931284,,,,C536673,,,,
mondo:0042963,wandering spleen,"['spleens, displaced', 'spleens, drifting', 'floating spleens', 'drifting spleen', 'spleens, wandering', 'drifting spleens', 'floating spleen', 'displaced spleens', 'spleen, displaced', 'spleens, floating', 'spleen, drifting', 'spleen, wandering', 'ptosis, splenic', 'wandering spleens', 'wandering spleen', 'splenoptosis', 'splenic Ptoses', 'splenic ptosis', 'spleen, floating', 'displaced spleen', 'Splenoptoses', 'Ptoses, splenic']",,,,C0272414,,C85224,,D050805,,,,
mondo:0042964,Machado-Joseph disease type 4,,,,,C0686352,,,,,334.3,,,
mondo:0042965,Machado-Joseph disease type 5,,,,,,,,,,334.3,,,
mondo:0042966,inherited mitral valve disease,['hereditary mitral valve disease'],,,,,,,,,,,,
mondo:0042967,rheumatic disease of mitral valve,"['mitral valve rheumatologic disorder', 'rheumatologic disorder of mitral valve']",,,,C0264765,,,,,,,,
mondo:0042968,partial duplication of chromosome 12,,,,,,,,,,,,,
mondo:0042969,partial duplication of the long arm of chromosome 12,"['chromosome 12q duplication', 'trisomy 12q', 'Duplication 12q', 'partial trisomy 12q', '12q trisomy', '12q duplication']",,,,C0795846,,,,C538300,,,,
mondo:0042970,disorder of glutamate decarboxylase,"['glutamate decarboxylase deficiency', 'disorder of glutamate decarboxylase activity', 'glutamate decarboxylase activity disease', 'deficiency of glutamate decarboxylase']",,,,C1291560,,,,,277.6,,,
mondo:0042971,congenital herpes virus infection,['Herpesviridae caused infectious embryofetopathy'],,,,C4275250,,,,,,,,
mondo:0042972,meningococcemia,,,,,C0025306,,,,,036.2,,,
mondo:0042973,familial osteosclerosis,['hereditary osteosclerosis'],,,,,,,,,,,,
mondo:0042974,parainfluenza virus type 3 infectious disease,"['infection caused by parainfluenza virus 3', 'PIV3', 'human parainfluenza virus type 3', 'infection caused by human parainfluenza virus 3', 'infection due to parainfluenza virus 3', 'human respirovirus 3 caused disease or disorder', 'infection due to human parainfluenza virus 3']",,,,C0276324,,,,,079.89,,,
mondo:0042975,pseudoachondroplastic dysplasia 2,"['spondyloepiphyseal dysplasia pseudoachondroplastic 2', 'recessive pseudoachondroplasia', 'pseudoachondroplastic dysplasia 2']",,264150,,C2931030,,,,C535820,,,,
mondo:0042976,vitamin B deficiency,"['deficiencies, vitamin B', 'vitamin B deficiencies', 'deficiency, vitamin B']",,,,C0042850,,C35129,,D014804,,,,
mondo:0042977,"trichoepithelioma, multiple familial, 1","['MFT1', 'Brooke-Fordyce Trichoepitheliomas', 'epithelioma adenoides cysticum of Brooke', 'epithelioma, hereditary multiple benign cystic', 'trichoepithelioma multiple familial 1', 'multiple familial trichoepithelioma 1', 'trichoepithelioma, multiple familial, 1']",,601606,,,,,,,,,,
mondo:0042979,"hypokalemic periodic paralysis, type 1","['HOKPP1', 'hypokalemic periodic paralysis, type 1']",,170400,,C3714580,,,,,,,,
mondo:0042980,Westphal disease,"['Westphal variant of Huntington^s disease', 'HD- Westphal variant', 'Westphal disease']",,,,C1279186,,,,C536694,,,,
mondo:0042981,aortic valve stenosis,"['AS', 'valvular aortic stenosis', 'rheumatic aortic stenosis', 'rheumatic aortic valve stenosis', 'aortic stenosis']",1712,,,C0155567,"['-0.269', '0.1324', '0.1836', '0.2007', '0.10547', '-0.0734', '0.2798', '0.1869', '-0.09357', '-0.1243', '-0.197', '-0.377', '0.003206', '0.2817', '-0.08594', '-0.2559', '-0.0889', '-0.02167', '-0.1672', '-0.2117', '-0.002596', '-0.07404', '0.2744', '-0.0697', '0.1417', '0.0467', '0.0997', '0.217', '0.10876', '0.253', '0.3953', '-0.01639', '0.2454', '0.1785', '0.013145', '-0.46', '0.2106', '0.0684', '0.1868', '-0.3125', '0.1166', '-0.03099', '0.2225', '-0.06683', '-0.0653', '-0.0005035', '0.07074', '0.01883', '-0.01707', '0.1361', '-0.0797', '-0.04355', '0.03812', '-0.013824', '-0.1813', '-0.0976', '0.08594', '-0.0523', '-0.02155', '-0.1024', '0.1288', '0.3076', '0.0405', '-0.1184', '0.03053', '-0.04507', '0.3281', '0.1329', '-0.4258', '-0.07764', '-0.1727', '0.0345', '0.09503', '-0.31', '-0.0775', '0.1567', '0.11426', '0.0894', '-0.1937', '-0.2654', '-0.1301', '-0.0847', '0.0974', '0.11755', '-0.07227', '-0.02829', '0.0638', '0.0648', '0.1669', '-0.1582', '-0.0885', '0.1081', '-0.1671', '0.02286', '0.538', '-0.02933', '0.1924', '-0.2361', '-0.1145', '0.262']",C50462,0000266,D001024,746.3,I06.0,,0001650
mondo:0042982,GATA2 deficiency with susceptibility to MDS/AML,"['GATA2 deficiency/MonoMac syndrome', 'GATA2 deficiency']",,,,,,C126349,,,,,,
mondo:0042983,neurocutaneous syndrome,"['neurocutaneous syndrome', 'neurocutaneous disorder', 'phakomatosis', 'syndromes, neurocutaneous', 'neurocutaneous disorders', 'Phakomatoses', 'syndromes, neuroectodermal dysplasia', 'syndrome, neurocutaneous', 'syndrome, neuroectodermal dysplasia', 'Phacomatosis', 'neuroectodermal dysplasia syndromes', 'Phacomatoses', 'neuroectodermal dysplasia syndrome']",,,,C0265316,,C84348,,D020752,,,,
mondo:0043003,familial acanthosis nigricans,"['hereditary acanthosis nigricans (disease)', 'acanthosis nigricans']",,100600,,C2930792,,,,C531598,,,,
mondo:0043004,Weil^s disease,"['jaundice, spirochetal', 'spirochetal jaundice', 'Icterohemorrhagic leptospirosis', 'disease, Weil', 'leptospirosis, icterohemorrhagic', 'Weil^s disease', 'disease, Weil^s', 'Weils disease']",,,,,,,,D014895,,,,
mondo:0043009,hereditary lethal multiple congenital anomalies/dysmorphic syndrome,['genetic lethal multiple congenital anomalies/dysmorphic syndrome'],,,471383,,,,,,,,,
mondo:0043069,Zerres Rietschel Majewski syndrome,"['postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and intellectual disability', 'postnatal short stature, microcephaly, severe syndactyly of hands and feet, dysmorphic face, and mental retardation']",,,,C2931301,,,,C536724,,,,
mondo:0043071,Zazam Sheriff Phillips syndrome,"['aniridia, lens luxation, mental retardation', 'aniridia, lens luxation, intellectual disability', 'aniridia, ectopia lentis, abnormal upper incisors and mental retardation', 'aniridia, ectopia lentis, abnormal upper incisors and intellectual disability']",,,,C2931300,,,,C536723,,,,
mondo:0043073,Zadik-Barak-Levin syndrome,"['dermoid cysts, hypothyroidism, cleft palate, and hypodontia', 'dermoid cysts, hypothyroidism, cleft palate and hypodontia']",,,,C2931298,,,,C536721,,,,
mondo:0043075,neuroaxonal dystrophy renal tubular acidosis,"['CNS disorder characterized by severe behavioral retardation, hypotonia, inability to talk, marked tremors, gait disturbances and inability to concentr', 'CNS disorder characterised by severe behavioural retardation, hypotonia, inability to talk, marked tremors, gait disturbances and inability to concentr', 'Maccario Mena weir syndrome']",,,,C2931479,,,,C537386,,,,
mondo:0043077,weinstein kliman scully syndrome,"['cardiomyopathy, hypogonadism and metabolic anomalies', 'primary testicular insufficiency with normal virilization, blindness, deafness and metabolic abnormalities']",,,,C2931289,,,,C536688,,,,
mondo:0043079,acute articular rheumatism,['acute rheumatism'],,,,,,,,,,,,
mondo:0043083,"coronal synostosis, syndactyly and jejunal atresia","['asymmetrical coronal synostosis, cutaneous syndactyly of the fingers and toes, and jejunal atresia']",,,,C2931194,,,,C536445,,,,
mondo:0043085,"chromosome 1, uniparental disomy 1q12 q21","['Mosaic trisomy 1q12 q21', 'uniparental disomy 1q12 q21']",,,,CN035970,,,,C538085,,,,
mondo:0043087,thickened earlobes with conductive deafness from incus-stapes abnormalities,"['Schweitzer Kemink Graham syndrome', 'conductive hearing loss, middle ear ossicular anomalies, malformed thickened lop auricles, and micrognathia', 'thickened earlobes with conductive deafness from incus-stapes abnormalities']",,,,C2931222,,,,C536511,,,,
mondo:0043089,acute posterior multifocal placoid pigment epitheliopathy,"['AMPPE', 'acute placoid pigment epitheliopathy', 'APMPPE', 'multifocal placoid pigment epitheliopathy', 'epitheliopathy, acute posterior multifocal placoid pigment', 'acute multifocal placoid pigment epitheliopathy']",,,,C0154884,,,,,,,,
mondo:0043094,"ichthyosis, follicular",['follicular ichthyosis'],,,,,,,,,,,,
mondo:0043096,holoacardius amorphus,['foetus anideus'],,,2161,,,,,,,,,
mondo:0043099,Hordnes Engebretsen Knudtson syndrome,"['acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and intellectual disability', 'acrobrachycephaly, ventriculomegaly, pulmonary stenosis, ectopic anus and mental retardation']",,,,C2931100,,,,C536067,,,,
mondo:0043101,hypothalamic dysfunction,,,,,,,,,,,,,
mondo:0043103,hypothyroidism due to iodide transport defect,['iodide Transport defect'],,,,C0271826,,C121747,,,,,,
mondo:0043106,ichthyosis linearis circumflexa,,,,,,,,,,,,,
mondo:0043108,infantile striato thalamic degeneration,,,,1575,,,,,,,,,
mondo:0043110,jones hersh yusk syndrome,"['aplasia cutis cleft palate epidermolysis', 'ptosis, ectropion, thin skin, beaked nose', 'aplasia cutis congenita, cleft palate, epidermolysis bullosa, and ectrodactyly']",,,,C2931054,,,,C535885,,,,
mondo:0043112,lachiewicz sibley syndrome,['hereditary renal disease and preauricular pits'],,,,C2931742,,,,C538131,,,,
mondo:0043114,Landy-Donnai syndrome,"['hydrops, ectrodactyly, syndactyly, duplication of the great toes']",,,,C2931460,,,,C537266,,,,
mondo:0043116,Iida Kannari syndrome,"['craniosynostosis with joint contractures, ear deformity, cleft palate, scoliosis, and other features']",,,,C2931159,,,,C536284,,,,
mondo:0043120,male pseudohermaphroditism due to defective lh molecule,,,,,C1835303,,,,C535692,,,,
mondo:0043123,massa casaer ceulemans syndrome,['arthrogryposis multiplex congenita associated with lissencephaly'],,,,C2931090,,,,C536031,,,,
mondo:0043125,mcpherson robertson cammarano syndrome,"['dominantly inherited ptosis, strabismus and ectopic pupils']",,,,C2931751,,,,C538161,,,,
mondo:0043127,mehta lewis patton syndrome,"['congenital heart disease, ptosis, hypodontia, and craniosynostosis']",,,,C2931120,,,,C536147,,,,
mondo:0043129,merlob grunebaum reisner syndrome,['familial opposable triphalangeal thumbs associated with duplication of the big toes'],,,,C2931499,,,,C537461,,,,
mondo:0043131,Michels Caskey syndrome,"['Mullerian aplasia with unilateral hypoplasia of the thumbs and skeletal spine deformities', 'Mullerian aplasia with hypoplastic thumbs']",,,,C2931537,,,,C537576,,,,
mondo:0043133,microcephaly micropenis convulsions,"['microcephaly micropenis convulsions', 'microcephaly seizures genital hypoplasia', 'microcephaly micropenis seizures']",,,,C2931525,,,,C537540,,,,
mondo:0043135,microcephaly microphthalmos blindness,,,,,C2931526,,,,C537541,,,,
mondo:0043137,isolated microcephaly,"['nonsyndromic microcephaly', 'Nonsyndromal microcephaly']",,,,,,,,C537542,,,,
mondo:0043139,microcephaly sparse hair intellectual disability seizures,,,,,C2931530,,,,C537545,,,,
mondo:0043141,microdontia hypodontia short stature,"['microdontia, hypodontia, short bulbous roots and root canals with strabismus, short stature, and borderline mentality']",,,,C2931532,,,,C537553,,,,
mondo:0043143,microphthalmia microtia fetal akinesia,"['microphthalmia-microtia-fetal akinesia', 'Thomas Jewett Raines syndrome', 'fetal akinesia with characteristic facial appearance, severe microphthalmia, microtia, and truncus arteriosus', 'Thomas-Jewett-Raines syndrome', 'foetal akinesia with characteristic facial appearance, severe microphthalmia, microtia, and truncus arteriosus']",,,2547,C2931224,,,,C536513,,,,
mondo:0043152,negative rheumatoid factor polyarthritis,"['rheumatoid factor negative erosive chronic polyarthritis', 'RF-ve CP', 'rheumatoid factor-negative polyarthritis']",,,,C2931825,,,,C538347,,,,
mondo:0043154,neonatal ovarian cyst,"['fetal ovarian cyst', 'foetal ovarian cyst']",,,,C2931186,,,,C536396,,,,
mondo:0043156,nephrotic syndrome ocular anomalies,"['familial infantile nephrotic syndrome with ocular abnormalities', 'Glastre Cochat Bouvier syndrome']",,,,C2931188,,,,C536403,,,,
mondo:0043162,pagon stephan syndrome,['septo-optic dysplasia with digital anomalies'],,,,C2931733,,,,C538100,,,,
mondo:0043164,palmer pagon syndrome,"['hydrocephaly - low insertion umbilicus', 'familial hydrocephalus with a low-insertion umbilicus']",,,2184,C2931734,,,,C538107,,,,
mondo:0043166,pancreatic lipomatosis duodenal stenosis,['pancreatic lipomatosis and duodenal atresia'],,,,C2931040,,,,C535839,,,,
mondo:0043168,panostotic fibrous dysplasia,"['unusual facial appearance, bone fragility, hyperphosphatasemia, and hypophosphatemia']",,,,C2931430,,,,C537164,,,,
mondo:0043170,Pavone Fiumara Rizzo syndrome,"['syndactyly type 1 with cataracts and mental retardation', 'syndactyly type 1 with cataracts and intellectual disability', 'Pavone Fiumara Rizzo syndrome']",,,,C2931172,,,,C536313,,,,
mondo:0043172,pfeiffer rockelein syndrome,"['asymmetrical coronal synostosis, cutaneous syndactyly of fingers and toes, and jejunal atresia']",,,,C2931656,,,,C537890,,,,
mondo:0043174,Pfeiffer Tietze Welte syndrome,"['sagittal craniostenosis, bilateral coloboma of the iris, craniofacial dysmorphy, asymmetrical split hand malformation, bilateral syndactyly of 2nd-4th']",,,,C2931657,,,,C537891,,,,
mondo:0043176,phosphoribosylpyrophosphate synthetase deficiency,"['deafness hyperuricemia neurologic ataxia', 'PRPP synthetase deficiency']",,,,C2931079,,,,C537897,,,,
mondo:0043179,piepkorn karp hickok syndrome,"['short ribs, polysyndactyly, cranial synostosis, cleft palate cardiovascular and urogenital anomalies and severe ossification defect']",,,,C2931016,,,,C535774,,,,
mondo:0043183,podder-tolmie syndrome,"['meningoencephalocele, arthrogryposis and hypoplastic thumbs']",,,,C2931519,,,,C537518,,,,
mondo:0043185,pointer syndrome,"['skeletal abnormalities, camptodactyly, facial anomalies, and feeding difficulties']",,,,C0796118,,,,C536323,,,,
mondo:0043187,pulmonary artery agenesis,,,,,,,,,,,,,
mondo:0043191,radial defect robin sequence,"['Bruce winship syndrome', 'bilateral radial defects, club foot deformity, micrognathia and cleft palate', 'Bruce Winship syndrome', 'bilateral radial defects club foot deformity micrognathia and cleft palate']",,,,C2931143,,,,C536261,,,,
mondo:0043193,richieri-costa guion-almeida cohen syndrome,"['Richieri Costa Guion-Almeida dwarfism', 'overgrowth - craniosynostosis - arthrogryposis', 'Richieri-costa Guion-Almeida Cohen syndrome', 'acrofacial dysostosis Richieri Costa Guion-Almeida type']",,,,C2930979,,,,C535676,,,,
mondo:0043195,Rubinstein Taybi like syndrome,"['Broad terminal phalanges of the thumbs and great toes, antimongoloid slant of the palpebral fissures, and characteristic beaked noses']",,180850,,C2931052,,,,C535877,,,,
mondo:0043197,ruvalcaba churesigaew myhre syndrome,"['onset of senility in the early teens, atrophic skin, hypogonadism, retinal and vascular sclerosis']",,,,C2931437,,,,C537190,,,,
mondo:0043199,short limb dwarf lethal colavita kozlowski type,['Colavita Kozlowski syndrome'],,,,C2931544,,,,C537597,,,,
mondo:0043206,trichostasis spinulosa,['elevated dark spiny papules on the face or trunk'],,,,C0263487,,,,C536558,,,,
mondo:0043207,urethral obstruction sequence,"['EUOS', 'early urethral obstruction sequence', 'renal dysplasia or hydronephrosis, oligohydramnios and subsequent lung hypoplasia due to urethral obstruction']",,,,C0265363,,,,C536477,,,,
mondo:0043209,albinism,['albinism'],,,,C0001916,,C84543,,D000417,,E70.3,,
mondo:0043218,neurovascular disorder,"['neurovascular disorder', 'nervous system disorder of vasculature', 'vasculature nervous system disorder']",,,,C3898144,,C117007,,,,,,
mondo:0043219,migraine with brainstem aura,"['basilar artery migraine with aura', 'vertebrobasilar migraine', 'brainstem migraine', 'Bickerstaff migraine', 'basilar-type migraine', 'basilar artery migraine', 'MBA']",,,,,,C117013,,,,,,
mondo:0043224,multi-infarct dementia,"['multi-infarct, dementia', 'Multiinfarct Dementias', 'multi infarct dementia', 'Dementias, multi-infarct', 'dementia, Multiinfarct', 'Multiinfarct dementia', 'dementia, multi infarct', 'multi-infarct dementia', 'dementia multi-infarcts', 'dementia multi infarct', 'multi-infarct Dementias', 'lacunar Dementias', 'Binswanger disease', 'Binswanger^s disease', 'dementia, lacunar', 'Dementias, lacunar', 'lacunar dementia', 'dementia multi-infarct', 'multi-infarcts, dementia', 'Dementias, Multiinfarct']",,,,,,C34522,,D015161,,,,
mondo:0043226,postpartum amenorrhea-galactorrhea syndrome,"['disease, Frommel^s', 'Frommel disease', 'syndrome, Chiari-Frommel', 'disease, Frommel', 'Chiari Frommel syndrome', 'Frommel^s disease']",,,,,,,1001291,D002640,,,,
mondo:0043230,ciguatera fish poisoning,"['Poisonings, ciguatera fish', 'ciguatera fish poisoning', 'ciguatera fish Poisonings', 'ciguatera poisoning', 'Poisonings, ciguatera', 'poisoning, ciguatera fish', 'ciguatera', 'poisoning, ciguatera', 'ciguatera Poisonings']",,,,,,,,D036841,,,,
mondo:0043233,exfoliative dermatitis,"['Erythrodermas', 'exfoliative Dermatitides', 'dermatitis exfoliativa', 'Dermatitides, exfoliative', 'erythroderma', 'exfoliative dermatitis']",,,,C0011606,,C39646,,D003873,,,,
mondo:0043237,glossodynia,"['glossopyrosis', 'glossodynia', 'Glossopyroses', 'Glossodynias', 'Glossalgias']",,,,,,,,D005926,,,,
mondo:0043240,hemophilic arthropathy,"['arthropathy in haemophilia', 'hemophilic arthritis']",,,,C0263725,,C27039,,,,,,
mondo:0043243,leukoplakia,"['lesions, leukoplakic', 'leukoplakia', 'leukoplakias', 'leukokeratoses', 'leukoplakic lesion', 'leukoplakic lesions', 'lesion, leukoplakic', 'keratotic plaque', 'leukokeratosis']",,,,C0023531,,C3186,,D007971,,,,
mondo:0043247,Mallory-Weiss syndrome,"['gastroesophageal laceration-hemorrhages', 'Mallory-Weiss syndrome', 'gastroesophageal laceration-hemorrhage', 'Mallory Weiss tear', 'Mallory-Weiss tear', 'syndrome, Mallory-Weiss', 'mucosal Lacerations-gastroesophageal junctions', 'gastroesophageal laceration haemorrhage', 'Mallory-Weiss laceration', 'laceration-hemorrhage, gastroesophageal', 'junctions, mucosal Lacerations-gastroesophageal', 'mucosal Lacerations-gastroesophageal junction', 'laceration-hemorrhages, gastroesophageal', 'Mallory Weiss syndrome', 'junction, mucosal Lacerations-gastroesophageal', 'laceration, Mallory-Weiss', 'mucosal Lacerations gastroesophageal junction', 'Lacerations-gastroesophageal junctions, mucosal', 'gastroesophageal laceration hemorrhage', 'mucosal lacerations - gastroesophageal junction', 'Lacerations-gastroesophageal junction, mucosal', 'Mallory Weiss laceration']",,,,C0024633,,C84881,,D008309,,,,
mondo:0043251,odontoma,"['ameloblastic fibro-odontoma', 'ameloblastic fibro-odontomas', 'fibroodontomas', 'odontoma, compound', 'odontoma', 'odontoma, benign', 'fibro odontoma, ameloblastic', 'fibro odontoma', 'fibro-odontomas, ameloblastic', 'compound odontomas', 'fibro-odontomas', 'fibro-odontoma', 'odontomas', 'compound odontoma', 'odontomas, compound', 'fibroodontoma', 'fibro-odontoma, ameloblastic']",,,,,,C3287,,D009810,,,,
mondo:0043254,papular urticaria,['bullous papular urticaria - type'],,,,,,,,C537169,,,,
mondo:0043257,pemphigus and fogo selvagem,"['endemic pemphigus foliaceus', 'FS', 'South American pemphigus', 'Brazilian pemphigus foliaceus', 'Brazilian pemphigus']",,,636955,C0263314,,,,C535551,,,,
mondo:0043264,post-traumatic epilepsy,"['late post-traumatic seizure', 'seizure disorder, post-traumatic', 'late post-traumatic seizures', 'disorders, post-traumatic seizure', 'post-traumatic seizures, late', 'seizures, late post-traumatic', 'late post traumatic seizures', 'post-traumatic Epilepsies', 'disorder, post-traumatic seizure', 'traumatic epilepsy', 'impact seizures', 'Epilepsies, traumatic', 'post-traumatic seizures, early', 'traumatic Epilepsies', 'convulsions, concussive', 'early post-traumatic seizure', 'epilepsy, traumatic', 'impact seizure', 'early post traumatic seizures', 'post-traumatic epilepsy', 'epilepsy, post traumatic', 'post traumatic seizure disorder', 'concussive convulsions', 'Epilepsies, post-traumatic', 'convulsion, concussive', 'post-traumatic seizure disorders', 'early post-traumatic seizures', 'seizure, late post-traumatic', 'seizure disorder, post traumatic', 'concussive convulsion', 'seizure, early post-traumatic', 'seizures, early post-traumatic', 'post-traumatic seizure, early', 'post-traumatic seizure, late', 'post-traumatic seizure disorder', 'seizure disorders, post-traumatic']",,,,C0751126,,,,D004834,,,,
mondo:0043267,rheumatoid vasculitis,"['vasculitis, rheumatoid', 'rheumatoid Vasculitides', 'Vasculitides, rheumatoid']",,,,C0240903,,,,D056653,,,,
mondo:0043275,TORCH syndrome,"['TORCH infection', 'toxoplasmosis, Other infections, Rubella, Cytomegalovirus, and Herpes simplex Virus (TORCH) syndrome', 'TORCH syndrome']",0080835,,,C0270173,,C98609,,,,,,
mondo:0043277,mosaic trisomy 6,"['trisomy 6', 'trisomy 6 mosaicism']",,,,,,C36475,,,,,,
mondo:0043280,Wallerian degeneration,"['Wallerian Degeneration', 'Degeneration, Wallerian', 'Wallerian degeneration of the pyramidal tract']",,,,,,C85223,,D014855,,,,
mondo:0043283,silicosiderosis,"['hematite pneumoconiosis', 'iron miners lung']",,,,C0018929,,,1001855,C537337,,,,
mondo:0043287,superior vena cava syndrome,"['superior vena cava syndrome', 'SVC syndrome', 'SVCS', 'superior vena cava obstruction', 'superior vena cava thrombosis', 'SVC obstruction']",,,,,,C3396,,D013479,,,,
mondo:0043291,Rokitansky-Aschoff sinuses of the gallbladder,"['intramural diverticulosis of the gallbladder', 'Rokitansky-Aschoff sinuses']",,,,C0267892,,,,C535869,,,,
mondo:0043294,linear scleroderma,"['Scleroderma, linear', 'en coup de sabre', 'en coup de saber', 'linear Scleroderma']",,,,,,C116780,,,,,,
mondo:0043297,vibrio vulnificus infectious disease,['Vibrio vulnificus caused disease or disorder'],,,,C1274377,,,,C536348,,,,
mondo:0043300,actinic cheilitis,['actinic cheilosis'],,,,C0267026,,C183562,,C535669,,,,
mondo:0043303,hyperacusis,"['perception disturbance, loudness', 'auditory Hyperesthesias', 'hyperacusia', 'disturbances, loudness perception', 'loudness perception disturbances', 'hyperacusias', 'hyperacuses', 'auditory hyperesthesia', 'loudness recruitment', 'hyperesthesia, auditory', 'low tolerance to sound', 'perception disturbances, loudness', 'Phonophobias', 'loudness perception disturbance', 'phonophobia', 'hyperacusis', 'disturbance, loudness perception', 'recruitment, loudness', 'hyperesthesias, auditory', 'loudness Recruitments']",,,,,,C116366,,D012001,,,,
mondo:0043310,amaurosis fugax,"['monocular blindness, transient', 'blindness, monocular, transient', 'transient monocular blindness', 'amaurosis fugax', 'blindness, transient monocular']",,,,,,C84550,,D020757,,,,
mondo:0043314,aquarium granuloma,"['Mycobacterium marinum infection', 'M. marinum', 'fish tank granuloma', 'Mycobacterium marinum caused skin disease']",,,,C0275708,,,,C535526,,,,
mondo:0043317,amyopathic dermatomyositis,"['dermatomyositis sine myositis', 'amyopathic dermatomyositis', 'ADM']",,,645617,C0406645,,,,C538250,,,,
mondo:0043320,piriformis syndrome,"['piriformis syndrome', 'syndrome, piriformis', 'piriformis syndromes', 'muscle syndromes, piriformis', 'syndrome, piriformis muscle', 'deep gluteal syndrome', 'piriformis muscle syndromes', 'Pseudosciatica', 'hip socket neuropathy', 'wallet sciatica', 'syndromes, piriformis', 'syndromes, piriformis muscle', 'pyriformis syndrome', 'muscle syndrome, piriformis', 'piriformis muscle syndrome']",,,,C0458224,,C85012,,D055958,,,,
mondo:0043327,cerebrospinal fluid leak,"['cerebrospinal fluid leak, post traumatic', 'cerebrospinal fluid leakage, post-traumatic', 'CSF otorrhea', 'cerebrospinal fluid leak, post-traumatic', 'CSF leak', 'cerebrospinal fluid drainage, spontaneous', 'cerebrospinal fluid Drainages', 'leak, cerebrospinal fluid', 'fluid Drainages, cerebrospinal', 'fluid leakage, cerebrospinal', 'fluid Leakages, cerebrospinal', 'spinal cerebrospinal fluid leak, post-traumatic', 'cerebrospinal fluid leakage', 'Drainages, cerebrospinal fluid', 'CSF rhinorrhea', 'cerebrospinal fluid leakage, spontaneous', 'cerebrospinal fluid drainage, traumatic', 'leakage, cerebrospinal fluid', 'Leakages, cerebrospinal fluid', 'cerebrospinal fluid Leaks', 'cerebrospinal fluid leak, traumatic', 'drainage, cerebrospinal fluid', 'cerebrospinal fluid leak, spontaneous', 'fluid leak, cerebrospinal', 'spinal cerebrospinal fluid leak, post traumatic', 'cerebrospinal fluid drainage', 'fluid Leaks, cerebrospinal', 'fluid drainage, cerebrospinal', 'spinal CSF leak', 'Leaks, cerebrospinal fluid', 'cerebrospinal fluid drainage, post traumatic', 'cerebrospinal fluid Leakages', 'spinal cerebrospinal fluid leak', 'cerebrospinal fluid leakage, post traumatic', 'spinal cerebrospinal fluid leak, spontaneous', 'cerebrospinal fluid leakage, traumatic', 'spinal cerebrospinal fluid leak, traumatic', 'cerebrospinal fluid drainage, post-traumatic']",,,,,,,,D065634,,,,
mondo:0043330,Mirizzi syndrome,"['syndrome, Mirizzi', 'syndrome, Mirizzi^s', 'Mirizzis syndrome', 'Mirizzi^s syndrome']",,,521219,C0267878,,,1001860,D057792,,,,
mondo:0043339,lathyrism,['Neurolathyrism'],,,,,,,1001776,D007842,,,,
mondo:0043343,Chilaiditi syndrome,"['Chilaiditi^s anomaly', 'syndrome, Chilaiditi^s', 'Chilaiditi anomaly', 'Chilaiditi^s syndrome', 'Chilaiditis anomaly', 'anomaly, Chilaiditi', 'Chilaiditis syndrome', 'anomaly, Chilaiditi^s', 'syndrome, Chilaiditi']",,,,,,,,D059269,,,,
mondo:0043346,progressive transformation of germinal centers,"['progressive transformation of Germinal centers', 'PTGC', 'progressive transformation of Germinal centres']",,,,,,C38408,,C548085,,,,
mondo:0043349,intravascular papillary endothelial hyperplasia,"['Masson^s pseudosarcoma', 'Masson pseudotumor', 'papillary endothelial hyperplasia', 'Masson^s pseudoangiosarcoma', 'intravascular papillary endothelial hyperplasia', 'Masson^s tumour', 'Masson lesion', 'Masson^s tumor', 'Masson^s vegetant hemangioma', 'Masson^s vegetant intravascular hemangio-endothelioma', 'Masson^s pseudotumor']",,,,C0343083,,C4391,,,,,,
mondo:0043352,fournier gangrene,"['Fourniers disease', 'gangrene, Fournier^s', 'gangrene, Fournier', 'Fournier^s gangrene', 'Fournier disease', 'Fournier^s disease', 'Fourniers gangrene']",,,,C0238419,,,,D018934,,,,
mondo:0043355,collagenous gastritis,['collagenous gastritis'],,,,C4040043,,C122082,,,,,,
mondo:0043358,engraftment syndrome,['engraftment syndrome'],,,,C0919746,,C63324,,,,,,
mondo:0043361,May-Thurner syndrome,"['Iliac vein compression syndrome', 'compression syndromes, Iliocaval', 'Iliocaval compression syndromes', 'May Thurner syndrome', 'compression syndrome, Iliocaval', 'syndromes, Iliocaval compression', 'syndrome, Iliocaval compression', 'Iliocaval compression syndrome', 'Cockett syndrome', 'syndrome, May-Thurner', 'syndrome, Cockett']",,,,C3165062,,,,D062108,,,,
mondo:0043364,eosinophil peroxidase deficiency,"['Presentey anomaly', 'eosinophil peroxidase deficiency', 'EPXD', 'peroxidase and phospholipid deficiency in eosinophils', 'eosinophil peroxidase deficiency, Partial', 'eosinophil peroxidase deficiency, partial']",,261500,,C1850000,"['-0.0936', '0.0738', '0.005524', '-0.01021', '0.035', '-0.08307', '-0.004364', '0.06088', '-0.02995', '-0.0308', '0.004036', '-0.00639', '-0.01614', '-0.01695', '-0.038', '-0.0218', '-0.00804', '-0.02203', '-0.0686', '-0.1649', '-0.02467', '-0.03784', '0.10315', '-0.00893', '0.012665', '-0.02051', '0.01057', '-0.02666', '0.004314', '-0.04987', '0.0667', '0.00257', '0.09247', '0.0669', '0.0196', '-0.06714', '-0.0006776', '-0.0389', '-0.012054', '-0.1004', '0.01874', '-0.0837', '0.0447', '-0.01111', '-0.0268', '-0.0834', '0.00717', '0.0714', '0.02971', '0.05432', '0.00937', '-0.02701', '0.02222', '0.04477', '-0.0707', '-0.02274', '0.10754', '-0.04538', '-0.1136', '0.01868', '0.03574', '0.05792', '0.001906', '-0.00664', '0.01251', '-0.01561', '0.0856', '0.06946', '-0.0992', '0.0662', '-0.08356', '0.0045', '0.01682', '-0.0631', '0.02962', '0.04044', '0.008736', '0.001511', '-0.0518', '-0.03043', '-0.00513', '-0.013374', '-0.013794', '0.05', '0.01996', '-0.01034', '0.02667', '0.0783', '0.1113', '-0.008446', '0.04395', '0.0785', '-0.00426', '0.002596', '0.1508', '0.0788', '0.0805', '-0.11383', '-0.01633', '0.05316']",,,C564893,,,,
mondo:0043370,secondary adrenal insufficiency,"['central Hypoadrenalism', 'secondary adrenal insufficiency', 'central adrenal insufficiency']",,,,C0948387,,C62602,,,,,,
mondo:0043373,sudden sensorineural hearing loss,"['deafness, sudden', 'acute sensorineural hearing loss by acute acoustic trauma or sudden deafness or surgery induced acoustic trauma', 'sudden deafness', 'sudden hearing loss']",,,90059,C4275242,,,,D003639,,,,
mondo:0043377,juvenile spondyloarthropathy,"['JSpA', 'juvenile spondyloarthropathy', 'juvenile Spondyloarthritis']",,,,C0409676,,C114347,,,,,,
mondo:0043424,digestive system infectious disorder,"['digestive system infection', 'gastrointestinal system infection', 'gastrointestinal infection']",,,,,,C35503,,,,,,
mondo:0043452,"chromosome 8, trisomy","['chromosome 8 duplication', 'trisomy 8']",,,,,,C36396,,C537942,,,,
mondo:0043455,humoral hypercalcemia of malignancy,['hypercalcemia of malignancy'],,,,C0149911,,C3496,,C562390,,,,
mondo:0043458,radiation injury,"['injury, radiation', 'sickness, radiation', 'radiation syndrome', 'syndrome, radiation', 'radiation Sicknesses', 'radiation syndromes', 'radiation injury', 'syndromes, radiation', 'Injuries, radiation', 'radiation sickness', 'Sicknesses, radiation']",,,,C0034535,,,,D011832,,,,
mondo:0043459,radiation-induced disorder,"['radiation-induced abnormalities', 'radiation-induced Abnormality', 'radiation induced abnormalities', 'abnormalities, radiation induced', 'radiation-induced disorder', 'Abnormality, radiation-induced']",,,521132,C1527225,,C26684,,D000016,,,,
mondo:0043465,achlorhydria,"['hypochlorhydria', 'achlorhydria', 'achylia gastrica']",,,,,,C2850,,D000126,,,,
mondo:0043468,acne keloid,"['nuchal keloid acne', 'folliculitis Keloidalis', 'lichen Keloidalis nuchae', 'keloid, acne', 'folliculitis Keloidalis nuchae', 'dermatitis papillaris Capillitius', 'papillaris Capillitii, dermatitis', 'papillaris Capillitius, dermatitis', 'nuchae, folliculitis Keloidalis', 'Keloidalis nuchae, lichen', 'dermatitis papillaris Capillitii', 'Keloidalis nuchae, folliculitis', 'keloidal folliculitis', 'acne keloids', 'Acnes, nuchal keloid', 'nuchal keloid Acnes', 'nuchae, lichen Keloidalis', 'Capillitius, dermatitis papillaris', 'keloid acne, nuchal', 'keloid Acnes, nuchal', 'keloidal acne', 'keloidal Acnes', 'acne, keloidal', 'acne, nuchal keloid', 'keloids, acne', 'acne keloid', 'Capillitii, dermatitis papillaris', 'acne Keloidalis']",,,,C0001145,,C34346,1001256,D000153,,,,
mondo:0043472,ectopic ACTH secretion syndrome,"['syndromes, ectopic ACTH', 'ectopic ACTH secretion', 'syndrome, ectopic ACTH', 'ectopic ACTH syndrome', 'ectopic ACTH syndromes', 'ectopic ACTH secretion syndrome', 'hypercortisolism due to nonpituitary tumour', 'ACTH syndromes, ectopic']",,,,C0001231,,C4387,,D000182,,,,
mondo:0043475,Adams-Stokes syndrome,"['Adam Stokes attacks', 'Stokes Adams attacks', 'syndrome, Adams-Stokes', 'Stokes Adams syndrome', 'Stokes-Adams syndrome', 'Stokes-Adams attacks', 'attacks, Adam-Stokes', 'syndrome, Stokes-Adams', 'Adams Stokes syndrome', 'attacks, Stokes-Adams', 'Adam-Stokes attacks']",,,,C0001396,,C79765,1001259,D000219,,,,
mondo:0043479,adenoviridae infectious disease,"['Adenoviridae infection', 'adenovirus infections', 'infection, Adenoviridae', 'infection, adenovirus', 'adenovirus infection', 'Adenoviridae caused disease or disorder', 'infections, Adenoviridae', 'infections, adenovirus']",,,,C0001486,,C115149,,D000257,,,,
mondo:0043494,arteritis,"['artery inflammation', 'Inflammation, arterial', 'Arteritides', 'arteritis', 'arterial Inflammation']",,,,,,C34399,0009011,D001167,,,,0012089
mondo:0043510,brain injury,"['brain Traumas', 'brain injury', 'brain trauma']",,,90056,,,,,D001930,,,,
mondo:0043512,traumatic encephalopathy,['traumatic encephalopathy'],,,,,,C35542,1001277,,,,,
mondo:0043519,burn,"['burn', 'Burn(s)', 'Burn']",,,,,,C34441,1001768,D002056,,T20-T25,,
mondo:0043523,cadmium poisoning,"['cadmium Poisonings', 'Itai Itai', 'poisoning, cadmium', 'Itai-Itai', 'Poisonings, cadmium']",,,,,,,,D002105,,,,
mondo:0043529,carcinoid heart disease,"['carcinoid heart diseases', 'heart diseases, carcinoid', 'heart disease, carcinoid']",,,,C0007093,,,1001775,D002275,,,,
mondo:0043537,cluster headache syndrome,"['red migraine', 'headache syndromes, cluster', 'cluster headache', 'cluster headaches, chronic', 'syndromes, cluster headache', 'headaches, chronic cluster', 'syndrome, Horton', 'erythroprosopalgia of bing', 'cluster headache, episodic', 'ciliary neuralgias', 'cluster headache, chronic', 'headaches, episodic cluster', 'Horton^s syndrome', 'migraines, neuralgic', 'episodic cluster headaches', 'chronic cluster headache', 'histamine headache', 'atypical cluster headaches', 'atypical cluster headache', 'episodic cluster headache', 'headache, cluster', 'syndrome, cluster headache', 'cluster headache, atypical', 'cluster headache syndromes', 'cluster headaches', 'neuralgia, ciliary', 'headache, chronic cluster', 'headaches, atypical cluster', 'cluster headache syndrome', 'histamine cephalgia', 'migraine, neuralgic', 'cluster headaches, atypical', 'headache, atypical cluster', 'Hortons syndrome', 'beuralgias, ciliary', 'Horton syndrome', 'chronic cluster headaches', 'headache syndrome, cluster', 'syndrome, Horton^s', 'migrainous neuralgia', 'ciliary neuralgia', 'Horton headache', 'neuralgic migraines', 'headaches, cluster', 'erythromelalgia of the head', 'neuralgic migraine', 'Cephalgia, histamine', 'headache, episodic cluster', 'cluster headaches, episodic', 'histamine cephalgias', 'Cephalgias, histamine', 'cluster migraine']",,,1002,,,C117077,0008571,D003027,,,,
mondo:0043541,viral conjunctivitis,"['Conjunctivitides, viral', 'viral Conjunctivitides', 'Viruses caused conjunctivitis (disease)', 'viral conjunctivitis']",,,,C0009774,,C34509,,D003236,,,,
mondo:0043543,iatrogenic disease,"['disease, iatrogenic', 'conditions, hospital-acquired', 'hospital-acquired conditions', 'iatrogenic diseases', 'hospital acquired condition', 'condition, hospital-acquired', 'hospital-acquired condition', 'diseases, iatrogenic']",,,,C0020732,,,,D007049,799.9,T80-T88,,
mondo:0043544,nosocomial infection,"['hospital-onset infection', 'Healthcare-associated infection', 'associated infections, Healthcare', 'infections, nosocomial', 'health care associated infections', 'infections, Cross', 'infections, hospital', 'health care associated infection', 'hospital-acquired infection', 'Healthcare associated infection', 'infections, Healthcare associated', 'infection, nosocomial', 'hospital infection', 'infection, Healthcare associated', 'Healthcare associated infections', 'nosocomial infections', 'associated infection, Healthcare', 'infection, hospital', 'nosocomial infection', 'Cross infections', 'infection, Cross', 'hospital infections', 'HAI']",,,,C0205721,,C115164,1001299,D003428,,,,
mondo:0043549,crush syndrome,"['syndrome, crush', 'syndromes, crush', 'ischaemic muscular necrosis syndrome', 'crush syndromes']",,,,,,,,D003444,,,,
mondo:0043555,infantile diarrhea,"['infantile onset diarrheal disease', 'toddler diarrhoea', 'infantile Diarrheas', 'infantile diarrhea', 'Diarrheas, infantile', 'diarrheal disease of infancy', 'infantile diarrheal disease']",,,,C0473132,,,,D003968,,,,
mondo:0043576,endarteritis,"['Endarteritides', 'endarteritis', 'tunica intima of artery inflammation']",,,,C0014100,,C34581,0009084,D004692,,,,
mondo:0043579,enteritis,"['enteritis', 'small intestine inflammation', 'Enteritides']",,,,C0014335,,C26765,,D004751,,,,
mondo:0043589,femoral neck fracture,"['femoral neck fracture', 'bone fracture of neck of femur', 'femur neck fractures', 'femur neck fracture', 'neck of femur bone fracture']",,,,,,,1001792,D005265,,,,
mondo:0043653,herpes labialis,"['cold sore', 'Herpes simplex, labial', 'fever blisters', 'blisters, fever', 'Sores, cold', 'labial Herpes simplex', 'Sore, cold', 'blister, fever', 'fever blister', 'cold sores']",,,,C0019345,,C34695,1001347,D006560,,,,
mondo:0043678,chromosome inversion disorder,"['chromosomal Inversions', 'Inversions, chromosomal', 'inv', 'inversion, chromosomal', 'chromosomal inversion', 'Inversions, chromosome', 'inversion', 'chromosome Inversions', 'inverted chromosome', 'inversion, chromosome']",,,,,,C6827,,D007446,,,,
mondo:0043683,Leriche syndrome,"['syndrome, Leriche', 'Leriches syndrome', 'Leriche syndrome', 'syndrome, Leriche^s', 'Leriche^s syndrome']",,,,C0023370,,C34773,,D007925,,,,
mondo:0043693,alcoholic liver diseases,"['alcoholic liver diseases', 'liver disease, alcoholic', 'alcoholic liver disease']",,,,,,C34783,0008573,D008108,,,,
mondo:0043723,Monteggia^s fracture,"['fracture, Monteggia^s', 'Monteggia fracture', 'Monteggias fracture']",,,,,,,1001373,D009011,,,,
mondo:0043726,multiple organ dysfunction syndrome,"['multiple organ dysfunction syndrome', 'organ failure, multiple', 'failure, multiple organ', 'MODS', 'organ dysfunction syndrome, multiple', 'multiple organ failures']",,,,,,C179648,,D009102,,,,
mondo:0043731,lytic metastatic bone lesion,"['Osteolyses', 'lytic metastatic bone lesion', 'osteolytic lesion']",,,,,,C35371,1001821,D010014,,,,
mondo:0043735,osteoradionecrosis,['Osteoradionecroses'],,,,,,C63707,,D010025,,,,
mondo:0043759,abdominal ectopic pregnancy,"['abdominal pregnancy', 'abdomen ectopic pregnancy', 'intra-abdominal pregnancy', 'Pregnancies, abdominal', 'ectopic pregnancy of abdomen', 'abdominal Pregnancies']",,,,,,C92921,,D011269,,,,
mondo:0043762,tubal pregnancy,"['Pregnancies, tubal', 'tubal Pregnancies', 'tubal pregnancy', 'fallopian tube ectopic pregnancy', 'ectopic pregnancy of fallopian tube']",,,,,,C92946,,D011274,,,,
mondo:0043765,presbycusis,"['presbycusis', 'Presbycuses']",,,,,,C116367,,D011304,,,,
mondo:0043768,thrombocytopenic purpura,"['purpuras, thrombopenic', 'thrombocytopenic purpura', 'purpuras, thrombocytopenic', 'thrombopenic purpuras', 'purpura, thrombopenic', 'thrombocytopenic purpuras', 'thrombopenic purpura']",,,,C0857305,,C26870,,D011696,,,,
mondo:0043771,radiodermatitis,"['dermatitis, radiation-induced', 'dermatitis, radiation induced', 'Dermatitides, radiation recall', 'radiation recall reactions', 'reactions, radiation recall', 'Radiodermatitides', 'dermatitis, radiation recall', 'Dermatitides, radiation-induced', 'recall reactions, radiation', 'radiation dermatitis', 'dermatitis radiation', 'radiation-induced Dermatitides', 'reaction, radiation recall', 'radiation recall dermatitis', 'radiodermatitis', 'recall reaction, radiation', 'radiation recall reaction', 'radiation induced dermatitis', 'radiation recall Dermatitides', 'radiation-induced dermatitis']",,,,,,C3349,1001840,D011855,,,,
mondo:0043775,respiratory paralysis,"['muscle paralyzes, respiratory', 'paralysis, respiratory', 'respiratory muscle paralysis', 'muscle paralysis, respiratory', 'paralysis, diaphragmatic', 'paralysis, respiratory muscle', 'diaphragmatic paralysis']",,,,,,,,D012133,,,,
mondo:0043777,rhinophyma,"['rhinophyma', 'Rhinophymas']",,,,C0035466,,C34989,,D012224,,,,
mondo:0043783,sclerema neonatorum,['sclerema neonatorum'],,,,,,C35009,,D012593,,,,
mondo:0043786,serositis,"['serous membrane inflammation', 'serositis', 'Serositides']",,,,,,C70428,,D012700,,,,
mondo:0043789,serum sickness,"['sickness, serum', 'serum sickness', 'serum Sicknesses', 'Sicknesses, serum']",,,,C0036830,,C79718,1001845,D012713,,,,
mondo:0043797,spinal cord injury,"['post traumatic myelopathy', 'spinal cord Contusions', 'spinal cord Traumas', 'cord transection, spinal', 'cord Transections, spinal', 'cord contusion, spinal', 'Contusions, spinal cord', 'spinal cord transection', 'laceration, spinal cord', 'myelopathy, traumatic', 'Myelopathies, traumatic', 'cord injury, spinal', 'spinal cord Transections', 'cord Traumas, spinal', 'traumatic Myelopathies', 'post-traumatic myelopathy', 'spinal cord laceration', 'injury of spinal cord', 'spinal cord trauma', 'transection, spinal cord', 'cord Injuries, spinal', 'Injuries, spinal cord', 'spinal cord injury', 'contusion, spinal cord', 'Transections, spinal cord', 'post-traumatic Myelopathies', 'Lacerations, spinal cord', 'Traumas, spinal cord', 'Myelopathies, post-traumatic', 'traumatic myelopathy', 'injury, spinal cord', 'cord Contusions, spinal', 'spinal cord contusion', 'trauma, spinal cord', 'spinal cord Lacerations', 'cord laceration, spinal', 'cord trauma, spinal', 'myelopathy, post-traumatic', 'cord Lacerations, spinal']",,,90058,,,,1001919,D013119,,,,
mondo:0043836,"tuberculosis, spinal","['disease, pott', 'Potts disease', 'disease, pott^s', 'pott disease', 'spinal Tuberculoses', 'Tuberculoses, spinal', 'spinal tuberculosis', 'pott^s disease', 'pott^s paraplegia']",,,,,,C35087,,D014399,,,,
mondo:0043839,ulcer disease,"['ulcer', 'ulcers']",,,,C0041582,"['-0.01697', '0.011604', '4.125e-05', '-0.005795', '0.01721', '-0.04025', '-0.003056', '0.01813', '-0.0194', '0.00842', '0.011696', '0.00449', '0.014984', '0.02368', '-0.02368', '-0.03162', '-0.01819', '0.000107', '-0.00387', '-0.05563', '-0.0012245', '-0.01575', '0.0216', '-0.009964', '0.02171', '-0.02052', '0.001731', '0.006027', '-0.003626', '-0.009', '0.02328', '-0.00010014', '0.01744', '-0.001156', '0.006805', '-0.01471', '-0.01435', '-0.01607', '0.005737', '-0.02992', '-0.02325', '-0.02736', '0.014366', '-0.01782', '-0.001873', '-0.03111', '0.003407', '0.00852', '0.01779', '-0.00951', '-0.0059', '0.005306', '0.01799', '0.01165', '0.0006104', '-0.0171', '0.0406', '-0.00874', '-0.0429', '-0.010925', '0.02908', '0.00938', '-0.0003407', '-0.006313', '-0.00885', '0.001777', '0.05225', '0.0212', '-0.02193', '0.02933', '-0.02911', '-0.01593', '0.00774', '-0.03513', '0.01723', '0.0215', '0.02946', '-0.007214', '-0.005947', '-0.01802', '0.003784', '0.005146', '-0.01042', '0.00912', '-0.01492', '0.00010884', '0.01628', '0.01735', '0.0367', '0.01232', '0.01596', '0.02884', '0.007442', '0.01611', '0.0556', '0.02242', '0.0226', '-0.01552', '-0.002344', '0.003334']",C3426,,D014456,,,,
mondo:0043862,voice disorders,['voice disorder'],,,,,,C3441,,D014832,,,,
mondo:0043875,tumor lysis syndrome,"['syndrome, tumour lysis', 'tumor lysis syndrome', 'syndromes, tumor lysis', 'syndrome, tumor lysis', 'syndromes, tumour lysis']",,,,C0041364,,C3425,1001479,D015275,,,,
mondo:0043878,hereditary optic atrophy,"['hereditary optic Atrophies', 'Atrophies, hereditary optic', 'hereditary optic atrophy', 'atrophy, hereditary optic', 'optic atrophy, hereditary']",,,,C0029125,,C34864,,D015418,,,,
mondo:0043885,eye infectious disorder,"['infection, ocular', 'infections, eye', 'eye infection', 'ocular infections', 'ocular infection', 'infections, ocular', 'infection, eye']",,,,C0015403,,C45372,,D015817,,,,
mondo:0043892,prosthesis-related infectious disease,"['prosthesis related infections', 'infections, prosthesis-related', 'device related infection', 'prosthesis-related infection']",,,,,,C79705,1002021,D016459,,,,
mondo:0043895,ankle injury,"['ankle sprain', 'ankle Sprains', 'Sprains, ankle', 'Injuries, ankle', 'injury, syndesmotic', 'syndesmotic Injuries', 'ankle injury', 'injury, ankle', 'tarsal region injury', 'syndesmotic injury', 'sprain, ankle', 'Injuries, syndesmotic']",,,,,,,1001832,D016512,,,,
mondo:0043904,"leishmaniasis, diffuse cutaneous","['diffuse cutaneous Leishmaniases', 'cutaneous leishmaniasis, diffuse', 'cutaneous Leishmaniases, diffuse', 'Leishmaniases, diffuse cutaneous']",,,,,,,,D016774,,,,
mondo:0043905,pneumonitis,"['lung parenchyma inflammation', 'pneumonitis']",,,,,,C113159,,,,,,
mondo:0043919,radiation pneumonitis,"['fibrosis, radiation', 'radiation fibrosis', 'radiation Pneumonias', 'radiation Pneumonitides', 'pneumonia, radiation', 'pneumonitis, radiation', 'Pneumonias, radiation', 'radiation pneumonia', 'Pneumonitides, radiation']",,,,,,,0008517,D017564,,,,
mondo:0043923,"lichen planus, oral",['oral lichen planus'],,,,C0206139,,C7406,1001415,D017676,,,,
mondo:0043953,burkholderia infectious disease,"['Burkholderia infection', 'Burkholderia caused disease or disorder', 'infection, Burkholderia', 'infections, Burkholderia']",,,,,,,1001280,D019121,,,,
mondo:0043959,pseudolymphoma,"['pseudolymphoma', 'lymphocytomas', 'hyperplasia, reactive lymphoid', 'lymphoid Hyperplasias, reactive', 'reactive lymphoid hyperplasia', 'lymphocytoma', 'pseudolymphomas', 'reactive lymphoid Hyperplasias', 'lymphoid hyperplasia, reactive', 'hyperplasias, reactive lymphoid']",,,,C0221269,,C3825,1001414,D019310,,,,
mondo:0043969,nocturnal paroxysmal dystonia,"['hypnogenic paroxysmal dystonias', 'paroxysmal dystonias, nocturnal', 'dystonias, sleep-related', 'hypnogenic paroxysmal dystonia', 'dystonia, nocturnal, paroxysmal', 'dystonia, sleep-related', 'nocturnal paroxysmal dystonias', 'dystonias, nocturnal paroxysmal', 'paroxysmal dystonia, nocturnal', 'dystonias, hypnogenic paroxysmal', 'paroxysmal dystonias, hypnogenic', 'sleep related dystonia', 'sleep-related dystonia', 'dystonia, nocturnal paroxysmal', 'paroxysmal dystonia, hypnogenic', 'sleep-related dystonias', 'dystonia, hypnogenic paroxysmal']",,,,C0393777,,,1001772,D020183,,,,
mondo:0043975,autonomic dysreflexia,"['autonomic Dysreflexias, spinal', 'autonomic Dysreflexias', 'Dysreflexias, spinal autonomic', 'Dysreflexia, spinal autonomic', 'Dysreflexias, autonomic', 'autonomic Hyperreflexias', 'hyperreflexias, autonomic', 'hyperreflexia, autonomic', 'autonomic Dysreflexia, spinal', 'Dysreflexia, autonomic', 'spinal autonomic Dysreflexia', 'spinal autonomic Dysreflexias', 'autonomic hyperreflexia']",,,,C0238015,,,1001762,D020211,,,,
mondo:0043982,cubital tunnel syndrome,"['cubital tunnel syndromes', 'ulnar nerve entrapment, elbow', 'tunnel syndrome, cubital', 'syndrome, cubital tunnel', 'syndromes, cubital tunnel', 'tunnel syndromes, cubital', 'ulnar nerve compression, cubital tunnel']",,,,,,,1001363,D020430,,,,
mondo:0043985,central nervous system lupus,"['CNS lupus', 'central nervous system lupus vasculitis', 'central nervous system lupus', 'systemic lupus Erythematosis, central nervous system', 'Meningoencephalitides, lupus', 'central nervous system systemic lupus Erythematosis', 'lupus meningoencephalitis', 'meningoencephalitis, lupus', 'lupus Meningoencephalitides', 'neuropsychiatric systemic lupus erythematosus']",,,,,,C116919,1001453,D020945,,,,
mondo:0043988,zoster sine herpete,['Zoster sine Eruptione'],,,,C1135841,,,1001827,D031368,,,,
mondo:0043994,acute cholecystitis,['acute cholecystitis'],,,,,,C35152,,D041881,,,,
mondo:0044001,"hearing loss, mixed conductive-sensorineural","['Losses, mixed hearing', 'mixed hearing loss', 'hearing loss, mixed conductive sensorineural', 'mixed conductive and sensorineural hearing loss', 'hearing loss, mixed', 'mixed conductive and sensorineural deafness', 'loss, mixed hearing']",,,,C0155552,,C26974,1001803,D046089,,,,
mondo:0044013,puerperal disorder,"['puerperal disorder', 'disorders, puerperal', 'disorder, puerperal']",,,,C0034040,,,,D011644,,,,
mondo:0044014,postpartum thyroiditis,"['thyroiditis, post-partum', 'thyroiditides, post-partum', 'thyroiditis, postpartum', 'post-partum thyroiditis', 'thyroiditides, postpartum', 'postpartum thyroiditis', 'postpartum thyroiditides', 'post partum thyroiditis', 'post-partum thyroiditides']",,,,C0271815,,C114389,,D050032,,,,
mondo:0044033,posterior leukoencephalopathy syndrome,"['RPLE', 'reversible Posterior cerebral edema syndrome', 'PRES', 'leukoencephalopathy syndromes, Posterior', 'Posterior reversible encephalopathy syndrome', 'syndrome, Posterior leukoencephalopathy', 'syndromes, Posterior leukoencephalopathy', 'reversible Posterior cerebral oedema syndrome', 'reversible Posterior leukoencephalopathy syndrome', 'reversible occipital parietal encephalopathy', 'leukoencephalopathy syndrome, Posterior', 'reversible posterior leukoencephalopathy syndrome']",,,,,,C78598,1001804,D054038,,,,
mondo:0044037,livedo reticularis,,,,,C0085642,,,,D054068,,,,
mondo:0044067,"candidiasis, invasive","['invasive candidiases', 'invasive candidiasis', 'candidiases, invasive']",,,636945,,,C116813,1001282,D058365,,,,
mondo:0044070,candidemia,['Candidemias'],,,,C0877445,,,1001311,D058387,,,,
mondo:0044079,cardio-renal syndrome,"['syndrome, Reno-Cardiac', 'cardio-renal syndromes', 'syndrome, Renocardiac', 'syndrome, cardiorenal', 'syndromes, Renocardiac', 'syndromes, cardiorenal', 'cardio renal syndrome', 'syndromes, cardio-renal', 'Renocardiac syndromes', 'syndrome, cardio-renal', 'Renocardiac syndrome', 'Reno-Cardiac syndrome', 'Reno Cardiac syndrome', 'cardiorenal syndrome', 'cardiorenal syndromes', 'syndromes, Reno-Cardiac', 'Reno-Cardiac syndromes']",,,,C2242703,,C123225,1001262,D059347,,,,
mondo:0044083,alternariosis,"['Alternarioses', 'dermal Alternariosis', 'Alternarioses, cutaneous', 'dermal Alternarioses', 'Alternariosis, dermal', 'subcutaneous Alternariosis', 'cutaneous Alternariosis', 'Alternarioses, dermal', 'Alternariosis, subcutaneous', 'subcutaneous Alternarioses', 'Alternariosis, cutaneous', 'Alternarioses, subcutaneous', 'cutaneous Alternarioses']",,,,,,,1001893,D060487,,,,
mondo:0044092,collagenous sprue,"['sprue, collagenous', 'collagenous sprue', 'collagenous Sprues', 'Sprues, collagenous']",,,,C0341299,,C45426,,D064068,,,,
mondo:0044098,ovarian ectopic pregnancy,"['ectopic pregnancy of ovary', 'Pregnancies, ovarian', 'ovary ectopic pregnancy', 'ovarian pregnancy', 'ovarian Pregnancies']",,,,,,C92945,,D065172,,,,
mondo:0044101,"pregnancy, cornual","['ectopic pregnancy of uterine horn', 'uterine horn ectopic pregnancy', 'cornual pregnancy', 'Pregnancies, cornual', 'cornual Pregnancies']",,,,,,C92761,,D065173,,,,
mondo:0044113,bullous systemic lupus erythematosus,"['bullous systemic lupus erythematosus', 'BSLE']",,,46489,C0409977,,C117104,0008619,,,,,
mondo:0044137,vitreous body disorder,"['vitreous body disease or disorder', 'disease of vitreous body', 'vitreous body disease', 'vitreous body disorder', 'disorder of vitreous body']",,,,C0155365,,C45256,0008624,,379.29,,,
mondo:0044138,hyalitis,"['Vitritis', 'hyaloiditis', 'hyalitis', 'Vitreitis']",,,,C0235812,,C50587,1001907,,,,,
mondo:0044141,panic disorder without agoraphobia,['panic disorder without agoraphobia'],,,,,,C97193,1001906,,,,,
mondo:0044144,panic disorder with agoraphobia,['panic disorder with agoraphobia'],,,,,,C97194,,,,,,
mondo:0044200,T-B+ severe combined immunodeficiency,['T-B+ SCID'],,,317416,,,,,,,,,
mondo:0044201,T+ B+ severe combined immunodeficiency,,,,397802,,,,,,,,,
mondo:0044202,episodic kinesigenic dyskinesia,"['familial PKD', 'paroxysmal kinesigenic choreathetosis', 'EKD', 'familial paroxysmal kinesigenic dyskinesia']",,,98809,,,,,,,,,
mondo:0044203,foveal hypoplasia,['FVH'],,,,,,,,,,,,
mondo:0044204,Shwachman-Diamond syndrome 1,"['pancreatic insufficiency and bone marrow dysfunction', 'Shwachman-Diamond syndrome', 'SDS1', 'lipomatosis of pancreas, congenital', 'Shwachman-Bodian syndrome', 'Shwachman-Diamond syndrome 1']",,260400,,,,,,,,,,
mondo:0044205,Shwachman-Diamond syndrome 2,"['Shwachman-Diamond syndrome 2', 'SDS2']",,617941,,CN244554,,,,,,,,
mondo:0044206,"otospondylomegaepiphyseal dysplasia, autosomal recessive","['Nance-Sweeney chondrodysplasia', 'Nance-Insley syndrome', 'Weissenbacher-Zweymuller syndrome, formerly', 'OSMEDB', 'OSMED', 'otospondylomegaepiphyseal dysplasia, autosomal recessive', 'chondrodystrophy with sensorineural deafness', 'Weissenbacher-Zweymuller syndrome']",,215150,,,,,,,,,,
mondo:0044207,specific granule deficiency 1,"['CEBPE specific granule deficiency', 'specific granule deficiency caused by mutation in CEBPE', 'specific granule deficiency 1', 'lactoferrin-deficient neutrophils', 'neutrophil lactoferrin deficiency', 'specific granule deficiency', 'SGD1']",,245480,,,,,,,,,,
mondo:0044208,specific granule deficiency 2,"['SGD2', 'specific granule deficiency 2']",,617475,,C4479548,,,,,,,,
mondo:0044209,disorder of lectin complement activation pathway,"['disorder of complement activation, lectin pathway']",,,,,,,,,,,,
mondo:0044210,thalassemia minor,['beta thalassemia trait'],0080774,,,,,,,,,D56.3,10054662,
mondo:0044211,idiopathic urticaria,,,,,C0157741,,,,,708.1,L50.1,,
mondo:0044212,chronic idiopathic urticaria,"['idiopathic urticaria, chronic']",,,,C0578870,,,,,,,,
mondo:0044213,acute idiopathic urticaria,"['idiopathic urticaria, acute']",,,,C0578869,,,,,,,,
mondo:0044299,"myasthenic syndrome, congenital, 22","['Prepl deficiency', 'CMS22', 'myasthenic syndrome, congenital, 22']",0080587,616224,,C4479088,,,,,,,,
mondo:0044300,familial adenomatous polyposis 4,"['FAP4', 'familial adenomatous polyposis 4', 'familial adenomatous polyposis type 4']",0080412,617100,480536,,,,,,,,,
mondo:0044301,"aortic aneurysm, familial thoracic 11, susceptibility to","['AAT11', 'aortic aneurysm, familial thoracic 11, susceptibility to']",,617349,,,,,,,,,,
mondo:0044302,"congenital heart defects, dysmorphic facial features, and intellectual developmental disorder","['congenital heart defects, dysmorphic FACIAL features, and intellectual developmental disorder', 'CHDFIDD', 'CDK13-related congenital heart defects-intellectual disability-facial dysmorphism syndrome']",0112247,617360,646278,C4479246,"['-0.04147', '0.06235', '0.03653', '-0.0353', '0.03119', '-0.0889', '0.0172', '0.1266', '-0.0714', '-0.06903', '-0.03111', '-0.02283', '0.00573', '0.006496', '-0.05405', '-0.02472', '-0.02461', '-0.02982', '-0.06064', '-0.1608', '0.003868', '0.00703', '0.0715', '-0.01727', '0.03894', '-0.02162', '-0.023', '-0.01581', '0.05222', '-0.0465', '0.071', '-0.00443', '0.1056', '0.0651', '0.01339', '-0.02701', '-0.02484', '-0.02423', '-0.006844', '-0.08795', '0.0429', '-0.06464', '0.01685', '-0.01776', '-0.00477', '-0.0716', '-0.003002', '0.0758', '-0.01935', '0.02863', '-0.06775', '-0.00989', '0.02107', '-0.01106', '-0.04303', '-0.0511', '0.04547', '-0.005802', '-0.0847', '0.02104', '0.03323', '0.01854', '-0.00586', '0.005962', '-0.007084', '0.011856', '0.0809', '0.1043', '-0.09937', '0.098', '-0.07166', '0.01834', '0.01121', '-0.05405', '0.01964', '0.03494', '0.05377', '-0.03244', '-0.07166', '-0.04694', '0.007305', '-0.01591', '-0.03415', '0.0864', '0.00547', '0.01851', '0.00953', '0.0865', '0.10754', '0.04398', '0.01726', '0.09686', '0.006386', '0.049', '0.1476', '0.0429', '0.08704', '-0.0956', '0.03268', '0.06107']",,,,,,,
mondo:0044303,congenital heart defects and ectodermal dysplasia,"['CHDED', 'congenital heart defects and ectodermal dysplasia']",,617364,,C4479250,"['-0.02614', '0.02524', '0.02475', '-0.008995', '0.04953', '-0.0339', '0.0001987', '0.04782', '-0.03296', '-0.04065', '-0.01243', '-0.02374', '0.004383', '0.01286', '-0.0196', '-0.01421', '-0.007515', '-0.019', '-0.04608', '-0.0877', '0.002125', '0.00565', '0.0507', '-0.01895', '0.02563', '-0.010475', '0.0004237', '-0.00489', '0.0206', '-0.03238', '0.0476', '-0.003', '0.03976', '0.02275', '0.02861', '-0.0161', '-0.013115', '-0.00553', '-0.003082', '-0.04175', '0.02454', '-0.0364', '0.00677', '-0.01402', '-0.01035', '-0.04407', '-0.013535', '0.04517', '0.00476', '0.01894', '-0.01335', '-0.01822', '0.03485', '0.01178', '-0.02727', '-0.02638', '0.047', '-0.00594', '-0.06018', '-0.0006504', '0.02888', '0.02963', '-0.005383', '0.006577', '0.0001576', '-0.00736', '0.05646', '0.05542', '-0.05957', '0.04608', '-0.02585', '-0.004173', '0.012314', '-0.02055', '0.0262', '0.01776', '0.004185', '-0.003124', '-0.01653', '-0.02803', '-0.01694', '0.01212', '-0.0182', '0.0483', '-0.01372', '0.002584', '0.024', '0.03857', '0.05304', '0.01675', '0.01071', '0.05', '0.002031', '0.0249', '0.10254', '0.015076', '0.04675', '-0.05496', '0.00458', '0.0363']",,,,,,,
mondo:0044304,hyperphenylalaninemia due to DNAJC12 deficiency,"['hyperphenylalaninemia, mild, non-BH4-deficient', 'HPANBH4']",,617384,508523,C4479270,"['-0.02565', '0.029', '0.005142', '-0.004158', '0.0003734', '-0.02942', '0.011826', '0.0419', '-0.0233', '-0.00924', '-0.00596', '-0.008125', '-0.001447', '0.01136', '-0.00921', '-0.00971', '-0.00977', '-0.01958', '-0.0209', '-0.0604', '-0.01729', '-0.01994', '0.0423', '-0.01432', '-0.005', '-0.00913', '0.0008593', '-0.00949', '-0.0008745', '-0.01213', '0.02235', '0.003218', '0.02174', '0.02505', '0.003548', '-0.01967', '0.005554', '-0.01079', '-0.001787', '-0.03683', '0.00539', '-0.0327', '0.01825', '-0.00851', '-0.01314', '-0.02174', '0.00885', '0.014885', '0.01435', '0.01624', '-0.000882', '-0.00446', '0.00817', '-0.0023', '-0.01799', '0.00259', '0.0327', '-0.00862', '-0.0463', '0.00795', '0.02689', '0.00686', '0.00872', '-0.005287', '0.006012', '0.002432', '0.03406', '0.0301', '-0.03516', '0.03256', '-0.02026', '0.00316', '-0.00395', '-0.03305', '0.02312', '0.01828', '0.0206', '-0.001769', '-0.02203', '-0.00731', '-0.00985', '-0.003258', '-0.00869', '0.03073', '0.006306', '0.0106', '0.00408', '0.02795', '0.04584', '0.00823', '0.01762', '0.02809', '-0.01069', '0.005356', '0.0687', '0.0187', '0.02106', '-0.0377', '-0.005222', '0.02423']",,,,,,,
mondo:0008368,autosomal dominant distal renal tubular acidosis,"['RTA, classic type', 'distal renal tubular acidosis (disease), autosomal dominant', 'RTA, gradient type', 'RTA, distal type, autosomal dominant', 'renal tubular acidosis, distal, autosomal dominant', 'distal renal tubular acidosis 1', 'AD dRTA', 'autosomal dominant SLC4A1-associated distal renal tubular acidosis', 'renal tubular acidosis 1']",,179800,93608,,"['-0.2476', '-0.04626', '-0.01724', '-0.2769', '-0.002634', '-0.3508', '-0.4065', '0.7334', '-0.01313', '0.0203', '-0.4395', '-0.1699', '-0.4907', '0.624', '-0.3767', '-0.1528', '0.2498', '0.02203', '-0.05737', '-1.068', '-0.0913', '-0.597', '0.4387', '0.2554', '0.4917', '-0.2742', '-0.101', '-0.03464', '0.1002', '-0.0415', '0.3625', '-0.2242', '0.1395', '-0.02931', '-0.529', '-0.7603', '-0.3184', '-0.2358', '-0.1332', '0.1622', '-0.2998', '-0.3162', '0.415', '-0.0651', '0.0815', '-0.525', '-0.2688', '-0.1011', '0.1036', '0.3247', '0.3262', '0.002563', '0.3142', '-0.3882', '0.05374', '-0.7896', '0.4414', '-0.1326', '-0.5615', '0.2947', '0.596', '-0.06445', '-0.01685', '-0.6396', '-0.3518', '-0.3054', '0.0372', '0.898', '-0.32', '0.2135', '-0.389', '-0.4905', '0.3264', '-0.10986', '0.2886', '0.293', '0.1356', '0.341', '0.03348', '0.1979', '0.1453', '0.1461', '0.4321', '-0.173', '0.3052', '0.6167', '0.2302', '-0.266', '0.4133', '0.1996', '0.1946', '0.168', '-0.04245', '-0.2285', '0.1807', '0.3254', '0.6777', '-0.306', '-0.462', '0.484']",,,,,,,
mondo:0008369,proximal renal tubular acidosis,"['RTA, proximal type', 'RTA, rate type', 'renal tubular acidosis 2', 'renal tubular acidosis, proximal', 'pRTA', 'Type 2 renal tubular acidosis', 'Type 2 RTA', 'renal tubular acidosis type 2']",,179830,47159,,"['-0.523', '-0.1776', '0.1615', '-0.3545', '-0.2725', '0.1984', '-0.2491', '0.764', '-0.3115', '-0.051', '-0.0826', '-0.008064', '0.013626', '0.6685', '0.02507', '-0.591', '-0.00994', '-0.1045', '0.3696', '-1.194', '-0.003757', '-0.2524', '0.4226', '0.0935', '0.1906', '0.08875', '-0.3887', '-0.4766', '0.1304', '-0.004566', '-0.0837', '-0.1373', '0.537', '-0.01935', '-0.3643', '-0.582', '-0.0676', '-0.1896', '0.1709', '0.0837', '-0.1901', '-0.4534', '0.4138', '-0.2261', '-0.11816', '-0.4663', '-0.1427', '-0.1472', '0.7227', '0.1567', '0.3657', '-0.04236', '-0.07733', '-0.845', '-0.2', '-0.0864', '0.799', '0.04626', '-0.5933', '0.5776', '0.2554', '-0.2322', '-0.16', '-0.8394', '-0.02243', '0.0694', '0.3647', '0.393', '-0.2008', '-0.3633', '-0.03857', '-0.1048', '0.506', '0.0918', '0.3142', '0.2075', '0.54', '-0.815', '0.1907', '0.3777', '0.2191', '0.3628', '-0.05865', '0.4263', '-0.447', '0.1942', '0.2417', '-0.5625', '0.8784', '0.6016', '0.3608', '0.01351', '-0.0209', '0.004173', '0.313', '0.05945', '0.6035', '-0.311', '-0.4573', '0.5137']",,,,588.89,,10037080,
mondo:0008371,Dowling-Degos disease,"['reticular pigment anomaly of flexures', 'DDD1', 'Dowling-Degos Kitamura disease', 'Dowling-Degos disease type 1', 'Dowling-Degos disease 1', 'dark dot disease']",0060256,,79145,,"['-0.1857', '0.2578', '0.10236', '-0.1305', '0.2172', '-0.3367', '-0.279', '-0.02664', '-0.3953', '0.0859', '-0.02892', '0.1367', '-0.2898', '-0.1982', '-0.2333', '0.1715', '0.4087', '-0.1393', '0.11176', '-0.5947', '-0.1683', '-0.1252', '0.2487', '-0.00344', '-0.1597', '0.1858', '-0.0759', '-0.03897', '-0.0974', '-0.081', '0.444', '-0.2715', '0.1157', '-0.0807', '0.3682', '0.389', '-0.273', '0.2039', '0.02666', '-0.4402', '0.05008', '-0.4001', '-0.005764', '0.01753', '-0.1864', '-0.2776', '-0.183', '0.1624', '0.2072', '0.07196', '-0.1743', '0.154', '0.2463', '0.079', '-0.4502', '-0.3013', '0.2135', '-0.0737', '-0.4983', '-0.251', '-0.05515', '-0.0635', '-0.2578', '0.11115', '-0.0595', '0.1776', '0.3525', '0.4148', '0.07117', '0.621', '-0.3691', '-0.1251', '0.2793', '0.1378', '-0.2179', '-0.1171', '-0.1656', '-0.0534', '0.1897', '-0.3843', '-0.08276', '-0.438', '0.1215', '0.2181', '0.0297', '-0.2323', '-0.2996', '0.2803', '0.295', '0.1913', '0.3198', '0.2048', '0.1039', '0.3538', '0.3528', '-0.1377', '0.4001', '-0.1191', '0.1062', '0.2512']",,,C562924,,,10068651,
mondo:0008372,retinal aplasia,"['amaurosis congenita', 'retinal aplasia']",,179900,,C1867331,,,,C566720,,,,
mondo:0008373,retinal arterial tortuosity,"['retinal haemorrhage with vascular tortuosity', 'retinal hemorrhage with vascular tortuosity', 'retinal arteriolar tortuosity', 'retinal arterial tortuosity (disease)', 'RATOR', 'retinal arterial tortuosity', 'tortuosity of retinal arteries', 'retinal arteries, tortuosity OF']",0111547,180000,75326,,"['-0.1205', '0.0894', '0.00915', '-0.04236', '0.05475', '-0.1682', '-0.01593', '0.1214', '-0.07086', '-0.0459', '-0.1284', '-0.0911', '0.01144', '0.004993', '-0.08325', '-0.0676', '-0.02602', '0.02281', '-0.01967', '-0.2585', '-0.04608', '-0.04227', '0.08276', '-0.006763', '-0.02238', '0.03088', '-0.0346', '-0.01831', '0.09656', '-0.03117', '0.1682', '0.0002763', '0.2112', '0.0538', '0.0743', '-0.07697', '0.01712', '-0.1332', '0.04095', '-0.2172', '0.0954', '-0.10657', '0.08746', '-0.0881', '-0.03598', '-0.05798', '-0.03458', '0.1384', '-0.009384', '0.02563', '-0.005898', '0.01828', '0.07935', '-0.00662', '-0.09467', '-0.03235', '0.1554', '-0.0563', '-0.183', '0.026', '0.1426', '0.0869', '-0.03207', '-0.02692', '0.01044', '-0.05823', '0.1718', '0.1403', '-0.12445', '0.1823', '-0.1643', '-0.02359', '-0.02788', '-0.1075', '0.01941', '-0.00801', '0.05667', '-0.01274', '-0.07355', '-0.0605', '-0.0283', '0.02339', '-0.044', '0.1624', '-0.04346', '0.003141', '0.05817', '0.1346', '0.1265', '-0.04', '0.105', '0.0903', '-0.02914', '0.04593', '0.2808', '0.05026', '0.208', '-0.144', '-0.03525', '0.09607']",,,,,,,0001136
mondo:0008374,retinal cone dystrophy type 1,"['RCD1', 'retinal cone Degeneration', 'cone dystrophy, autosomal dominant', 'cone dystrophy autosomal dominant', 'retinal cone dystrophy 1', 'retinal cone dystrophy-1']",0081024,180020,,,,,,C566719,,,,
mondo:0008375,retinal detachment,"['retina, detached', 'retinal detachment', 'detached retina']",5327,312530,,C0035305,,C26874,0005773,D012163,362.40,,,
mondo:0008376,retinal venous beading,['retinal venous beading'],,180080,,,,,,,,,,
mondo:0008377,retinitis pigmentosa 1,"['retinitis pigmentosa 1', 'RP1', 'RP', 'retinitis pigmentosa caused by mutation in RP1', 'retinitis pigmentosa type 1', 'retinitis pigmentosa', 'RP1 retinitis pigmentosa']",0110390,180100,,C0220701,,,,C538365,,H35.5,,
mondo:0008378,retinitis pigmentosa 9,"['RP 9', 'retinitis pigmentosa caused by mutation in RP9', 'retinitis pigmentosa 9', 'RP9 retinitis pigmentosa', 'RP9', 'retinitis pigmentosa type 9']",0110387,180104,,C1867300,,,,C566716,,H35.5,,
mondo:0008379,retinitis pigmentosa 10,"['retinitis pigmentosa type 10', 'retinitis pigmentosa caused by mutation in IMPDH1', 'IMPDH1 retinitis pigmentosa', 'retinitis pigmentosa 10', 'RP10']",0110388,180105,,C1867299,,,,C566715,,H35.5,,
mondo:0008380,retinoblastoma,"['RB - retinoblastoma', 'RB', 'Rb', 'RB1', 'eye cancer, retinoblastoma', 'retinoblastoma, malignant', 'retinoblastoma']",768,,790,C0035335,"['0.3748', '-0.065', '-0.0524', '0.676', '-0.2979', '-0.1455', '0.1871', '0.6724', '-0.08594', '-0.7246', '0.3708', '0.24', '-0.1642', '0.4746', '-0.311', '-0.3516', '-0.618', '-0.3025', '0.07623', '-0.74', '-0.5337', '-0.4094', '-0.2278', '-0.3315', '0.0004003', '0.526', '-0.04156', '0.431', '0.3564', '0.2888', '0.245', '-0.2164', '0.792', '-0.412', '-0.1304', '0.3777', '-0.6865', '-0.2084', '-0.1478', '-0.59', '0.5728', '-0.2098', '0.2915', '-0.936', '0.2191', '-0.0397', '-0.471', '-0.608', '0.2098', '-0.3845', '0.3977', '-0.01412', '0.159', '-0.1976', '0.3044', '-0.509', '-0.1433', '0.4692', '-0.491', '0.04907', '0.5166', '-0.05527', '0.4', '0.1633', '-0.047', '0.352', '0.6763', '0.538', '0.3137', '0.669', '0.3037', '0.2834', '-0.06287', '-0.2233', '0.5234', '0.02795', '-0.4827', '-0.1332', '-0.4702', '-0.079', '-0.1571', '0.1514', '0.3328', '0.4814', '-0.9663', '-1.157', '0.4595', '0.2678', '-0.0404', '0.4302', '-0.2048', '-0.08105', '-0.3452', '0.2676', '0.9053', '-0.1201', '0.2544', '-0.4348', '0.4253', '-0.5845']",C7541,,D012175,,,10038916,
mondo:0008381,dominant pericentral pigmentary retinopathy,"['retinopathy, pericentral pigmentary, dominant']",0110420,180210,,C1867261,,,,C566713,,H35.5,,
mondo:0008382,"retinoschisis, autosomal dominant","['retinoschisis autosomal dominant', 'retinoschisis, autosomal dominant']",,180270,,C1867235,,,,C000598640,,,,
mondo:0008383,rheumatoid arthritis,"['rheumatoid arthritis, progression of', 'arthritis, rheumatoid', 'atrophic arthritis', 'RA', 'rheumatoid arthritis', 'arthritis or polyarthritis, rheumatic', 'rheumatoid arthritis, susceptibility to']",7148,180300,284130,C0003873,"['0.05527', '0.1956', '-0.0298', '0.2668', '-0.07025', '-0.2152', '0.4348', '0.0999', '-0.626', '-0.02078', '0.555', '0.256', '-0.2852', '0.752', '0.0624', '-0.4663', '0.11676', '0.5005', '-0.1184', '-0.7446', '0.1477', '-0.1365', '0.4646', '-0.3706', '-0.074', '0.279', '-0.2457', '0.659', '-0.2137', '0.228', '0.2786', '-0.4197', '0.5327', '-0.163', '0.3396', '0.10077', '-1.28', '-0.288', '0.3062', '-0.747', '-0.2094', '-0.1923', '-0.3472', '0.0743', '-0.03754', '-0.02556', '0.0677', '0.1094', '0.357', '0.474', '-0.51', '0.1802', '0.6934', '0.383', '-0.3176', '-0.3347', '-0.4849', '0.2192', '-0.14', '-0.8105', '0.06604', '0.146', '-0.2825', '0.1486', '-0.2744', '0.3533', '0.1719', '1.061', '-0.1318', '0.7573', '0.1083', '-0.09424', '0.11865', '-0.284', '-0.2175', '0.5483', '-0.3127', '1.239', '-0.084', '-0.6562', '-0.629', '-0.1428', '-0.0812', '-0.5586', '-0.212', '0.0805', '-0.09625', '0.2783', '-0.274', '0.1982', '0.09186', '0.1368', '0.276', '0.3586', '0.6475', '-0.01913', '-0.0248', '-0.3704', '-0.7383', '-0.4832']",C2884,0000685,D001172,714.0,,,0001370
mondo:0008384,rheumatoid nodulosis,"['rheumatoid nodulosis', 'accelerated rheumatoid nodulosis']",,180350,,C1304215,,,,D012218,,,,
mondo:0008385,rhiny,"['craniorhiny', 'rhiny']",,180360,,,,,,C566708,,,,
mondo:0008386,Axenfeld-Rieger syndrome type 1,"['Rgs', 'Rieger syndrome type 1', 'Axenfeld-Rieger syndrome, type 1', 'RIEG1', 'Rieg', 'Rieger syndrome, type 1', 'PITX2 Axenfeld-Rieger syndrome', 'Axenfeld-Rieger syndrome caused by mutation in PITX2']",0110120,180500,,C3714873,,C75015,,,,,,
mondo:0008387,ring dermoid of cornea,"['ring dermoid of cornea', 'RING dermoid of cornea', 'bilateral, annular limbal dermoids with corneal and conjunctival extension', 'RDC', 'Ring dermoid syndrome']",0111548,180550,91481,C1867155,"['-0.02585', '0.04807', '0.001553', '0.003147', '-0.0004838', '-0.03723', '0.007183', '0.05673', '-0.0636', '-0.01423', '-0.02179', '-0.01449', '0.007133', '0.02426', '-0.04922', '-0.02017', '0.01091', '-0.0393', '-0.01306', '-0.08435', '-0.00955', '-0.010025', '0.05096', '0.00195', '0.0211', '-0.0277', '-0.01256', '0.01741', '0.01475', '-0.01457', '0.03464', '-0.010376', '0.03897', '0.01852', '0.04556', '-0.01447', '-0.01599', '-0.005325', '0.002714', '-0.07983', '0.0313', '-0.04767', '0.03436', '-0.01724', '-0.015045', '-0.0346', '-0.00477', '0.04147', '0.0249', '0.02919', '-0.01423', '-0.03397', '0.0289', '0.00596', '-0.03778', '-0.007515', '0.05447', '-0.0282', '-0.08264', '-0.010414', '0.03613', '0.01348', '-0.0376', '0.007076', '0.01081', '-0.000621', '0.0739', '0.04086', '-0.02872', '0.057', '-0.03696', '0.02005', '0.02988', '-0.05377', '-0.006237', '0.04947', '0.01634', '0.005867', '-0.03983', '-0.05115', '-0.0182', '-0.01403', '-0.03032', '0.0703', '-0.0286', '-0.01466', '-0.00207', '0.03458', '0.05902', '0.00928', '0.02252', '0.03845', '-0.006832', '0.013435', '0.0839', '-0.00833', '0.0409', '-0.0913', '-0.03018', '0.00946']",,,C535684,,,,
mondo:0008388,ringed hair disease,"['ringed hair', 'pili annulati']",,180600,169,C0263489,,,,C537187,,,,
mondo:0008389,autosomal dominant Robinow syndrome,"['Robinow syndrome, autosomal dominant type', 'autosomal dominant Robinow syndrome', 'Robinow syndrome, autosomal dominant']",,,3107,CN203673,"['-0.0706', '0.3633', '0.1321', '-0.89', '0.2861', '-0.3208', '0.0258', '0.7744', '-0.932', '-0.6606', '-0.2654', '0.2258', '0.04587', '0.2432', '0.1735', '0.436', '0.699', '-0.206', '0.1951', '-0.3184', '-0.3018', '0.2783', '0.5303', '-0.2294', '0.1304', '0.07355', '-0.1556', '-0.1026', '0.532', '-0.2715', '0.265', '-0.2408', '-0.004604', '-0.5933', '-0.1487', '-0.3833', '-0.3442', '-0.4126', '-0.3591', '-0.19', '0.4062', '-0.3652', '0.04178', '-0.0695', '0.1131', '-0.4038', '-0.2373', '0.4956', '0.1675', '-0.1545', '0.2686', '-0.2686', '-0.5186', '-0.1969', '-0.5312', '-0.4272', '0.1892', '-0.3357', '0.0956', '0.394', '0.2644', '0.01637', '-0.2262', '0.324', '0.03308', '-0.08746', '-0.10895', '0.2477', '-0.03882', '0.2852', '-0.557', '0.831', '0.31', '-0.2505', '0.06445', '0.656', '-0.0588', '-0.3845', '-0.517', '-0.3884', '0.3442', '0.2', '-0.01343', '0.362', '-0.10834', '0.6196', '-0.1633', '0.1539', '0.08124', '0.2218', '-0.1918', '0.4536', '0.11127', '0.02103', '0.6626', '0.2322', '0.53', '-0.694', '-0.07635', '0.0645']",,,,759.89,,,
mondo:0008390,Rombo syndrome,"['Rombo syndrome', 'vermiculate atrophoderma, milia, hypotrichosis, trichoepitheliomas, basal cell carcinomas and peripheral vasodilation with cyanosis']",,180730,3110,C1867147,,,,C535870,,,,
mondo:0008391,Robinow-Sorauf syndrome,"['Robinow-Sorauf syndrome', 'acrocephalosyndactyly, Robinow-Sorauf type', 'craniosynostosis-bifid hallux syndrome']",,180750,3106,CN203672,,,,C537183,,,,
mondo:0008392,Roussy-Levy syndrome,"['Roussy levy hereditary areflexic dystasia', 'hereditary motor sensory neuropathy I', 'hereditary areflexic dystasia', 'Roussy-levy syndrome', 'Charcot-Marie-Tooth disease (variant)', 'hereditary areflexic dystasia, Roussy-levy type', 'Roussy-Lévy syndrome', 'Roussy-levy hereditary areflexic dystasia', 'Charcot-Marie-Tooth-Roussy-levy disease', 'Roussy-levy disease', 'hereditary areflexic dystasia, Roussy-Lévy type', 'HMSN I', 'Roussy levy syndrome']",,180800,3115,,"['-0.276', '0.3308', '0.2253', '-0.0782', '-0.0879', '-0.4395', '0.1396', '0.4653', '-0.555', '0.1475', '-0.1877', '0.09235', '-0.325', '-0.01703', '0.2382', '0.05777', '-0.02122', '-0.04208', '-0.1437', '-0.518', '0.2559', '-0.0584', '-0.0607', '0.453', '-0.00949', '-0.0501', '0.08813', '-0.06256', '-0.3762', '-0.1604', '0.2927', '-0.08057', '0.11554', '0.013725', '0.08575', '-0.2964', '-0.2471', '-0.2078', '-0.12006', '-0.042', '-0.318', '-0.4075', '0.04926', '0.3704', '-0.02068', '-0.486', '-0.1959', '0.2491', '-0.09576', '0.0703', '0.0496', '0.354', '-0.2844', '-0.1768', '0.1177', '-0.325', '0.01804', '-0.01755', '-0.328', '-0.0893', '0.05017', '-0.2698', '0.2854', '0.3533', '-0.593', '0.331', '0.2407', '0.7144', '-0.04074', '0.4832', '-0.2725', '-0.0117', '0.3286', '-0.3645', '0.4993', '0.0731', '-0.02414', '0.411', '0.01878', '-0.3904', '-0.06866', '-0.4084', '0.2277', '0.7065', '-0.01506', '0.1799', '-0.167', '0.02602', '0.05447', '-0.05856', '0.293', '0.1671', '0.1398', '0.1735', '0.539', '0.07837', '0.4958', '-0.1416', '0.2026', '0.4343']",,,,334.3,,,
mondo:0008393,Rubinstein-Taybi syndrome due to CREBBP mutations,"['Rubinstein-Taybi syndrome 1', 'Rubinstein syndrome', 'broad thumbs and great toes, characteristic facies, and mental retardation', 'broad thumbs and great toes, characteristic facies, and intellectual disability', 'Rubinstein-Taybi syndrome type 1', 'broad thumb-hallux syndrome', 'RSTS', 'RSTS1', 'CREBBP Rubinstein-Taybi syndrome']",,180849,353277,,"['-0.4966', '0.1963', '0.3252', '-0.4502', '0.054', '-0.423', '0.09344', '0.2001', '-0.5107', '-0.3047', '-0.00925', '-0.1068', '0.04337', '-0.2908', '0.003202', '-0.07153', '0.1588', '0.1059', '-0.2306', '-0.2145', '0.1399', '0.2333', '0.1704', '-0.2379', '0.2517', '0.05777', '0.08734', '0.4243', '0.3767', '-0.212', '0.2258', '-0.2163', '0.304', '-0.09106', '0.3037', '-0.1802', '0.1368', '-0.137', '0.1719', '-0.489', '0.0974', '-0.0787', '0.06885', '0.003159', '0.000807', '-0.481', '0.0191', '0.535', '0.0862', '-0.06128', '-0.3025', '0.1697', '-0.2428', '0.1967', '-0.25', '-0.6514', '0.05362', '-0.00646', '-0.1469', '0.004765', '-0.036', '0.1477', '0.006714', '0.0388', '-0.01964', '0.0993', '0.2725', '0.0472', '-0.3079', '0.315', '-0.6064', '0.215', '0.2988', '-0.1616', '-0.2', '0.08124', '0.0432', '0.071', '-0.1713', '0.1456', '-0.1935', '0.1821', '0.3176', '0.1072', '0.05692', '-0.1624', '0.1533', '0.758', '0.01874', '0.1062', '-0.4207', '0.0985', '-0.0347', '0.04895', '0.639', '-0.2488', '0.462', '-0.4517', '0.2013', '0.2433']",C153290,,,,,,
mondo:0008394,Silver-Russell syndrome,"['Silver Russell syndrome', 'Russell-Silver dwarfism', 'Silver Russell dwarfism', 'Russell-Silver syndrome', 'Silver-Russell syndrome', 'Russell Silver syndrome', 'Silver-Russell dwarfism', 'SRS']",14681,,813,C0175693,"['-0.8315', '0.0755', '-0.06152', '0.0749', '0.3938', '0.0229', '0.05405', '0.925', '-0.816', '-0.5776', '-0.04095', '0.3293', '0.533', '-0.0876', '0.1812', '-0.01582', '0.6807', '-0.261', '-0.2668', '-0.4792', '0.2458', '-0.0737', '0.5806', '-0.351', '0.2213', '-0.1938', '0.08795', '-0.2563', '0.0812', '0.577', '0.7456', '-0.3096', '0.07495', '-0.2179', '-0.09076', '0.2776', '0.4084', '0.4897', '0.0787', '-0.2274', '0.2333', '0.1219', '-0.2576', '0.03912', '0.535', '-0.5376', '0.06082', '0.05005', '-0.131', '-0.2769', '0.0186', '-0.2297', '-0.6216', '0.5083', '-0.4382', '-0.5454', '-0.1509', '-0.3638', '0.05072', '0.1366', '-0.02338', '0.0908', '-0.1884', '-0.1945', '0.356', '-0.07', '0.2471', '0.008354', '0.04346', '0.2554', '-0.256', '0.1984', '-0.06024', '-0.01875', '0.0762', '0.831', '-0.0412', '-0.03455', '-0.678', '-0.543', '0.3206', '0.02452', '0.3916', '0.2472', '0.0857', '0.1702', '-0.7534', '0.1537', '0.5713', '0.141', '0.284', '0.3', '-0.4233', '-0.3623', '0.8096', '-0.2888', '0.10443', '-0.793', '0.856', '-0.0908']",C85068,,D056730,759.89,,10062282,
mondo:0008395,Ruvalcaba syndrome,['Ruvalcaba syndrome'],,180870,3121,C0265248,,,,C579395,759.89,,,
mondo:0008396,"oculodental syndrome, Rutherfurd type","['gingival Hypertrophy with corneal dystrophy', 'gingival hypertrophy corneal dystrophy', 'gingival hypertrophy-corneal dystrophy', 'corneal dystrophy with gum hypertrophy', 'corneal dystrophy with gum Hypertrophy', 'Rutherfurd syndrome']",,180900,2709,C0796140,,,,C537732,759.89,,,
mondo:0008397,aplasia of lacrimal and salivary glands,"['salivary glands, absence of', 'ALSG', 'parotid aplasia or hypoplasia', 'salivary glands, absence of, include', 'aplasia of lacrimal and salivary glands', 'congenital absence of lacrimal puncta and salivary glands']",0111549,180920,86815,,"['-0.1912', '0.2554', '0.418', '-0.4392', '-0.1007', '0.0868', '0.2742', '0.0599', '0.04803', '-0.12067', '-0.283', '-0.2183', '-0.798', '0.10864', '-0.2383', '0.11993', '0.2532', '0.1622', '-0.1345', '-0.6216', '-0.3633', '-0.625', '0.1536', '-0.3667', '0.03763', '0.0849', '-0.6357', '0.3828', '0.6494', '-0.857', '-0.1068', '0.225', '-0.03644', '0.3767', '0.05966', '0.1018', '-0.4197', '-0.279', '-0.05597', '-0.1816', '0.2186', '-0.01297', '0.3835', '-0.446', '-0.2734', '-0.792', '0.1881', '-0.1786', '-0.2788', '0.3962', '-0.266', '0.2966', '0.459', '0.2118', '-0.161', '-0.613', '0.08026', '-0.00484', '-0.601', '-0.3574', '-0.01073', '0.1571', '-0.4355', '-0.1854', '0.507', '0.04507', '0.82', '0.482', '-0.2472', '0.5425', '-0.4458', '-0.1364', '0.236', '-0.4949', '0.1725', '0.06213', '0.3718', '-0.1688', '0.2451', '0.06', '-0.2035', '-0.000555', '0.3247', '0.513', '-0.1437', '-0.2003', '0.2292', '0.07117', '0.0959', '-0.281', '-0.1241', '0.824', '0.3552', '0.1092', '0.952', '-0.0588', '0.1486', '-0.1884', '0.186', '0.2195']",,,,,,,
mondo:0008398,"salivary substance, Clostridium botulinum type","['salivary substance, Clostridium botulinum type']",,180950,,C1867056,,,,,,,,
mondo:0008399,"sarcoidosis, susceptibility to, 1","['SS1', 'sarcoidosis', 'sarcoidosis, susceptibility to, 1', 'sarcoidosis, susceptibility to, type 1', 'sarcoidosis caused by mutation in HLA-DRB1', 'Boeck sarcoid', 'susceptibility to sarcoidosis 1', 'HLA-DRB1 sarcoidosis']",,181000,,,,,,,135,,,
mondo:0008400,salivary duct calculi,"['submandibular duct calculi', 'parotid duct calculi', 'salivary duct calculi']",,181010,,,,,,D012465,,,,
mondo:0008401,pleomorphic adenoma,"['Psa', 'tumor, mixed, benign', 'pleomorphic adenoma', 'pleomorphic salivary gland adenoma', 'salivary gland adenoma, pleomorphic', 'mixed tumour of the salivary gland', 'pleomorphic adenoma (morphologic abnormality)', 'adenomas, salivary gland pleomorphic, somatic', 'mixed tumor of the salivary gland', 'Sgpa']",452,181030,454821,,,C8602,1000384,D008949,,D11.0,,
mondo:0008402,cleft palate-large ears-small head syndrome,"['cleft palate, microcephaly, large ears, and short stature', 'Say-Barber-Hobbs syndrome', 'Say Barber Hobbs syndrome', 'SAY syndrome', 'cleft palate large ears small head']",,181180,2013,C1867023,,,,C536621,,,,
mondo:0008403,scalp defects-postaxial polydactyly syndrome,"['scalp defects postaxial polydactyly', 'congenital scalp defects associated with postaxial polydactyly', 'scalp defects and postaxial polydactyly']",,181250,1003,C1867021,,,,C536622,,,,
mondo:0008404,scalp-ear-nipple syndrome,"['scalp-ear-nipple syndrome', 'hereditary syndrome of lumpy scalp, odd ears and rudimentary nipples', 'Finlay-Marks syndrome', 'scalp-EAR-nipple syndrome', 'Sen syndrome', 'scalp ear nipple syndrome', 'SENS']",0111550,181270,2036,,"['0.1992', '0.0481', '0.431', '-0.08813', '-0.0632', '-0.2169', '-0.527', '0.4917', '-0.2356', '-0.3716', '-0.28', '-0.10333', '-0.4604', '0.2189', '-0.1455', '0.4734', '0.2598', '0.01567', '-0.2375', '-0.6943', '-0.448', '0.2698', '0.2411', '-0.3884', '0.4805', '0.05304', '-0.533', '-0.1465', '0.478', '-0.4353', '0.578', '-0.418', '0.01533', '0.1532', '0.0923', '0.0402', '-0.414', '-0.1857', '-0.1633', '0.1924', '-0.12286', '0.0291', '0.09125', '0.005554', '0.1799', '-0.7207', '-0.1989', '0.267', '-0.2622', '-0.1656', '-0.4575', '-0.0379', '-0.1011', '0.0747', '-0.7964', '-0.2566', '0.4165', '0.1792', '-0.2499', '-0.28', '0.2334', '-0.141', '-0.5522', '0.02115', '0.3562', '0.1637', '0.289', '0.866', '-0.1469', '0.5396', '-0.509', '0.1896', '-0.12317', '0.0767', '0.4019', '-0.2452', '0.06076', '-0.04013', '-0.277', '0.0787', '-0.0763', '0.1287', '0.5425', '0.2866', '0.3972', '-0.0562', '-0.2693', '0.5234', '0.1595', '0.0667', '0.2883', '0.9155', '0.1395', '0.112', '0.5625', '-0.04648', '0.284', '-0.063', '0.4087', '0.3801']",,,C536623,,,,
mondo:0008406,autosomal recessive Emery-Dreifuss muscular dystrophy,"['Emery-Dreifuss muscular dystrophy, autosomal recessive', 'EDMD3']",,,98855,,"['-0.0143', '-0.8164', '-0.5854', '-0.12476', '0.666', '-1.31', '0.1837', '0.4795', '-1.943', '-0.8174', '0.07416', '0.444', '-0.2427', '0.9907', '0.2411', '0.3245', '-0.6333', '-0.3972', '-0.2632', '-0.636', '-0.0611', '0.2683', '0.1874', '0.4937', '0.2842', '-0.1375', '0.02177', '-1.098', '0.3987', '-0.3843', '0.7866', '-0.282', '0.5083', '0.07837', '0.3467', '0.0429', '-0.606', '0.428', '0.1359', '-0.5454', '0.1666', '-0.4124', '-0.556', '0.455', '-0.2196', '-0.0625', '0.0323', '0.7715', '-0.06195', '0.697', '0.32', '-0.4124', '0.1764', '-0.8174', '0.21', '-0.565', '0.4773', '1.039', '-0.4202', '-0.0767', '0.0505', '-0.03824', '-0.1456', '-0.106', '0.0802', '0.1552', '0.2219', '0.4492', '-0.347', '-0.08887', '-0.1412', '0.3286', '0.1248', '-0.2883', '0.784', '0.6216', '-0.2123', '0.6953', '-0.03635', '0.0584', '0.1027', '0.1208', '-0.2096', '0.11176', '-0.1229', '-0.012344', '-0.2732', '-0.4321', '1.016', '0.279', '-0.3728', '0.1573', '0.42', '0.9683', '-0.1832', '0.0696', '0.333', '-0.4595', '-0.2299', '-0.04614']",,,,,,,
mondo:0008407,"neurogenic scapuloperoneal syndrome, Kaeser type","['stark-Kaeser syndrome', 'scapuloperoneal syndrome, neurogenic, Kaeser type', 'scapuloperoneal syndrome, neurogenic type, of Kaeser', 'SCPNK', 'Kaeser syndrome']",0111551,181400,85146,C1867005,"['-0.433', '-0.003195', '0.10394', '-0.3103', '-0.0686', '-0.2822', '0.06216', '0.4033', '-0.4736', '0.01677', '-0.1771', '-0.01865', '-0.1584', '-0.1053', '0.11633', '0.1439', '0.01199', '0.010925', '-0.2559', '-0.5957', '0.174', '-0.1655', '0.1416', '0.1589', '0.0391', '0.10736', '0.1306', '-0.2754', '-0.1907', '-0.1833', '0.262', '0.1231', '0.3481', '0.05173', '0.0634', '-0.2192', '-0.2126', '-0.08734', '0.03174', '-0.3093', '-0.1274', '-0.3674', '-0.0006175', '0.1696', '-0.04095', '-0.1025', '0.01485', '0.2546', '-0.1967', '0.1339', '-0.1216', '0.12006', '-0.0763', '-0.2274', '-0.1794', '-0.1835', '0.218', '-0.2622', '-0.1691', '0.0373', '0.2646', '0.0562', '-0.02899', '-0.006134', '-0.4282', '-0.03885', '0.1641', '0.376', '-0.2189', '0.05972', '-0.1931', '0.05322', '0.04956', '0.0783', '0.1586', '-0.0593', '0.0633', '-0.00971', '-0.05624', '-0.2258', '0.2725', '-0.02847', '0.2295', '0.363', '-0.2034', '0.1841', '-0.189', '0.2546', '0.3992', '-0.1438', '0.4553', '0.2081', '0.1578', '0.1137', '0.3423', '0.166', '0.3884', '-0.03366', '-0.03412', '0.1935']",,,C566695,,,,
mondo:0008408,"scapuloperoneal spinal muscular atrophy, autosomal dominant","['scapuloperoneal neuronopathy', 'neurogenic scapuloperoneal amyotrophy, New England type', 'scapuloperoneal spinal muscular atrophy', 'SPSMA', 'amyotrophy, neurogenic scapuloperoneal, New England type']",0111552,181405,431255,,"['-0.3484', '0.0428', '0.0637', '-0.359', '0.1594', '-0.8', '0.0415', '0.8086', '-0.5234', '-0.511', '-0.0535', '0.0981', '-0.3652', '0.1462', '0.3628', '0.4124', '0.1065', '-0.5713', '-0.445', '-0.762', '-0.064', '-0.0781', '0.3809', '-0.011215', '0.06274', '-0.1577', '0.04285', '-0.08154', '-0.174', '-0.0374', '0.1947', '-0.09863', '-0.008514', '0.1302', '0.3467', '-0.5967', '-0.1493', '-0.3506', '0.10864', '-0.2167', '-0.651', '-0.537', '-0.371', '0.2715', '0.2494', '0.04614', '-0.2308', '0.2468', '-0.1003', '-0.1148', '0.539', '0.003311', '-0.1321', '-0.0696', '-0.3652', '-0.3044', '0.144', '-0.3452', '0.1848', '0.3174', '0.3247', '-0.1311', '-0.009674', '0.3528', '-0.739', '0.0588', '0.1288', '0.9966', '-0.1462', '-0.1741', '-0.173', '-0.0874', '-0.114', '0.017', '0.724', '0.1271', '0.3062', '-0.02629', '0.007698', '-0.1298', '0.4814', '-0.3286', '0.5376', '1.126', '-0.311', '0.4346', '-0.1749', '0.009445', '0.8125', '-0.02324', '0.0802', '0.0773', '0.06137', '0.4275', '0.6987', '0.0394', '0.765', '0.05283', '0.303', '0.1321']",,1001992,,335.19,,,
mondo:0008409,"congenital myopathy 7A, myosin storage, autosomal dominant","['SPMM', 'myopathy, myosin storage, autosomal dominant', 'myopathy with lysis of type 1 myofibrils', 'MYH7-related late-onset SPMD', 'MYH7-related late-onset scapuloperoneal syndrome', 'scapuloperoneal muscular dystrophy', 'SPMD', 'MYH7-related scapuloperoneal myopathy', 'scapuloperoneal myopathy, MYH7-related', 'MSMA', 'autosomal dominant myosin storage myopathy', 'MYH7-related late-onset scapuloperoneal muscular dystrophy', 'myopathy, hyaline body, autosomal dominant', 'scapuloperoneal syndrome, myopathic type']",0111269,608358,636965,C4759774,"['-0.03696', '0.0444', '0.01701', '-0.03232', '0.04187', '-0.1412', '0.01382', '0.0877', '-0.112', '-0.03928', '-0.04044', '-0.03087', '-0.03102', '0.03256', '0.02068', '-0.04254', '0.01054', '-0.07166', '-0.02986', '-0.1283', '-0.01994', '-0.04355', '0.0371', '0.03134', '-0.009796', '-0.05234', '-0.005276', '-0.0759', '-0.03375', '-0.05112', '0.05124', '0.02858', '0.058', '0.03882', '0.009865', '-0.001949', '-0.01924', '-0.02322', '-0.002277', '-0.0968', '0.01322', '-0.0837', '0.0072', '0.04758', '-0.001182', '-0.02438', '-0.02003', '0.05743', '0.0178', '0.01244', '0.00896', '-0.005096', '0.01901', '-0.007072', '-0.007286', '-0.05368', '0.09674', '-0.05478', '-0.0953', '0.02458', '0.0606', '0.00958', '0.0414', '0.04993', '-0.00807', '-0.00944', '0.10785', '0.1044', '-0.1019', '0.04123', '-0.057', '-0.0007825', '0.0326', '-0.055', '0.0783', '0.02155', '0.02042', '-0.04642', '-0.04102', '-0.02554', '0.03406', '-0.0003362', '-0.04123', '0.0669', '-0.04843', '0.01326', '0.0002677', '0.0678', '0.067', '0.007557', '0.04352', '0.04727', '0.03186', '0.0639', '0.1383', '0.05527', '0.10736', '-0.04337', '-0.02621', '0.01056']",,,C564253,359.89,,,
mondo:0008410,Scheuermann disease,"['juvenile kyphosis', 'familial spinal osteochondrosis', 'juvenile osteochondrosis of spine', 'spinal Osteochondrosis', 'Scheuermann^s kyphosis', 'juvenile osteochondritis of the spine', 'familial Scheuermann disease', 'Sherman^s disease', 'Scheuermann kyphosis', 'juvenile osteochondrosis of Scheurermann', 'Scheuermann^s disease', 'Calve^s disease', 'Scheuermann disease', 'Scheuermann juvenile kyphosis', 'familial Scheuermann juvenile kyphosis']",13300,181440,3135,C0036310,,C34999,0008576,D012544,732.0,,,
mondo:0008411,ulnar-mammary syndrome,"['ulnar-mammary syndrome', 'ulnar-mammary syndrome of Pallister', 'Schinzel syndrome', 'ums', 'Pallister ulnar-mammary syndrome']",0060614,181450,3138,C1866994,"['-0.6997', '-0.4536', '0.3694', '-0.518', '-0.2559', '-0.1279', '0.1166', '0.6997', '-0.205', '-0.5728', '-0.0776', '0.1364', '-0.443', '-0.0385', '-0.2375', '0.2563', '0.2185', '-0.2465', '-1.048', '-0.5767', '0.1349', '-0.0313', '0.522', '-0.3635', '0.419', '-0.3289', '-0.4438', '-0.1023', '0.5615', '-0.6533', '1.052', '-0.3254', '-0.3196', '0.366', '0.10187', '-0.1921', '0.0162', '0.1193', '0.0929', '0.1365', '0.1987', '0.2976', '-0.0866', '-0.1361', '0.472', '-0.1219', '0.5513', '0.643', '-0.10956', '0.013374', '-0.0641', '-0.1893', '-0.4072', '0.643', '-0.908', '-0.2615', '0.3137', '-0.491', '-0.2185', '0.102', '-0.005554', '-0.135', '0.009384', '-0.2734', '-0.467', '0.2396', '0.3064', '0.6885', '-0.5522', '0.0396', '-0.63', '0.4333', '0.08655', '-0.07355', '0.1278', '0.2812', '0.1804', '-0.4937', '-0.3015', '-0.3528', '0.001165', '0.04916', '0.68', '0.138', '0.1664', '0.03754', '-0.5225', '-0.1757', '0.389', '-0.571', '0.05585', '0.654', '0.372', '-0.3372', '0.7046', '-0.2482', '0.643', '-0.1526', '0.1848', '0.433']",,,C536937,759.89,,,
mondo:0008412,intestinal schistosomiasis,"['Schistosoma mansoni infection, susceptibility/resistance to', 'Schistosoma mansoni, intensity of infection by', 'Katayama fever', 'schistosomiasis japonica']",0050597,,,C0276932,,C35364,1001419,D012555,120.2,,,
mondo:0008414,schizophrenia 1,"['schizophrenia susceptibility locus, chromosome 5-related', 'schizophrenia 1', 'SCZD1', 'schizophrenia 1 with or without an affective disorder']",0070077,181510,,,,,,,,,,
mondo:0008416,palmoplantar keratoderma-sclerodactyly syndrome,"['HRZ', 'atrophic fibrosis of the skin of the limbs, hypoplasia of nails, and keratodermia of the palms and soles', 'Huriez syndrome', 'palmoplantar hyperkeratosis-sclerodactyly syndrome', 'SCLEROTYLOSIS', 'Scleroatrophic syndrome', 'Scleroatrophic and keratotic dermatosis of limbs', 'Sclerotylosis', 'Tys', 'HURIEZ syndrome']",,181600,384,,"['-0.1494', '0.04962', '0.1526', '-0.238', '0.1615', '-0.2856', '-0.084', '0.11945', '-0.05457', '-0.1062', '-0.03323', '-0.000582', '-0.2783', '-0.12384', '-0.3162', '0.0657', '0.361', '-0.276', '0.04276', '-0.3865', '-0.1656', '-0.0909', '0.3792', '-0.1107', '0.1638', '0.301', '-0.191', '0.1237', '-0.06256', '-0.3833', '0.2551', '-0.0649', '0.2856', '0.09784', '0.183', '0.0496', '-0.339', '-0.10425', '-0.0801', '-0.3247', '-0.1362', '-0.2803', '0.04434', '-0.1065', '-0.01599', '-0.2173', '-0.1299', '0.1462', '0.0316', '-0.2625', '-0.202', '0.02307', '0.2389', '0.06506', '-0.364', '-0.153', '0.1404', '-0.0918', '-0.2874', '-0.362', '0.106', '0.1079', '-0.2583', '-0.0195', '0.03262', '0.1437', '0.3137', '0.4688', '0.07007', '0.4993', '-0.3237', '-0.01611', '0.0495', '0.126', '0.05048', '-0.1394', '0.02606', '-0.1686', '0.02856', '-0.2544', '-0.079', '0.00789', '0.04523', '0.278', '0.0689', '-0.08746', '-0.05652', '0.3784', '0.2966', '-0.02081', '0.1594', '0.3357', '0.2568', '0.2183', '0.3154', '0.004353', '0.3645', '-0.286', '0.1675', '0.1678']",,,C537526,757.39,,,
mondo:0008417,"sclerocornea, autosomal dominant","['sclerocornea, autosomal dominant']",,181700,,,,,,C566692,,,,
mondo:0008418,"scleroderma, familial progressive","['systemic sclerosis, susceptibility to', 'Crest syndrome', 'scleroderma, familial progressive']",,181750,90290,C1866983,,,,,,,,
mondo:0008419,"scoliosis, isolated, susceptibility to, 1","['scoliosis, idiopathic 1', 'IS1', 'scoliosis, isolated, susceptibility to, 1', 'adolescent idiopathic scoliosis', 'adolescent isolated scoliosis']",,181800,,,,,,,,,,
mondo:0008420,seborrheic keratosis,"['keratosis Seborrheica', 'keratosis, seborrheic, somatic', 'basal cell papilloma', 'keratosis, seborrheic']",6498,182000,,C0022603,"['-0.2725', '0.3433', '0.05536', '0.3298', '0.3855', '-0.02028', '0.1821', '0.3733', '-0.3318', '-0.274', '0.9536', '1.138', '-0.6284', '0.4211', '-0.1381', '0.499', '0.4167', '-0.1126', '0.3557', '-0.2429', '-0.1366', '0.568', '0.2686', '-0.3608', '0.411', '0.1558', '-0.03134', '-0.2281', '0.1987', '-0.1101', '0.3645', '-1.154', '0.5654', '-0.006767', '0.4795', '0.2979', '-0.7803', '-0.5835', '0.1857', '-0.396', '0.4697', '-0.2834', '-0.2052', '-0.04337', '-0.1652', '-0.324', '-0.549', '0.319', '0.5137', '-0.1116', '0.133', '-0.291', '0.2084', '0.2522', '-0.4062', '0.125', '-0.3335', '0.1251', '-0.822', '-0.2988', '-0.2', '-0.0001312', '-0.186', '0.389', '0.3447', '0.7573', '0.685', '1.001', '0.1054', '0.9985', '0.2603', '-0.1304', '0.1332', '-0.03702', '-0.4153', '0.0639', '-0.548', '0.5615', '0.458', '-0.861', '0.571', '0.01094', '-0.006428', '-0.1824', '0.3486', '-0.1792', '0.182', '0.1306', '0.4966', '0.7334', '0.1181', '0.2072', '-0.241', '0.3987', '1.093', '0.1946', '-0.2593', '-0.363', '0.1466', '0.1582']",C9006,0005584,D017492,702.1,L82,,
mondo:0008421,flat face-microstomia-ear anomaly syndrome,"['Simosa-Penchaszadeh-Bustos syndrome', 'Simosa cranio facial syndrome', 'SIMOSA craniofacial syndrome', 'blepharophimosis-telecanthus-microstomia syndrome']",,182150,1968,C1866962,,,,C537339,,,,
mondo:0008422,autosomal dominant sideroblastic anemia,"['anemia, sideroblastic, 4', 'SIDBA4', 'anemia, sideroblastic, autosomal dominant', 'sideroblastic anemia, autosomal dominant']",0060335,182170,,C2674249,,,,C567160,,,,
mondo:0008423,sinus node disease and myopia,"['Sss-myopia syndrome', 'sick sinus syndrome and myopia', 'sinus node disease and myopia']",,182190,,C1866960,,,,C566690,,,,
mondo:0008424,"sella turcica, bridged","['sella turcica, bridged']",,182200,,,,,,C566689,,,,
mondo:0008425,"omphalocele syndrome, Shprintzen-Goldberg type","['Shprintzen omphalocele syndrome', 'omphalocele with hypoplasia of pharynx and larynx, learning disability, dysmorphic facies, and scoliosis', 'Shprintzen-Goldberg omphalocele syndrome', 'omphalocele, laryngeal and pharyngeal hypoplasia, learning disabilities, dysmorphic facies and spinal anomalies', 'pharynx and larynx hypoplasia with omphalocele', 'laryngeal and pharyngeal hypoplasia with omphalocele']",,182210,3164,C1866958,,,,C537329,,,,
mondo:0008426,Shprintzen-Goldberg syndrome,"['craniosynostosis with arachnodactyly and abdominal hernias', 'Shprintzen-Goldberg craniosynostosis syndrome', 'Shprintzen-Goldberg marfanoid syndrome', 'SGS', 'Marfanoid craniosynostosis syndrome', 'Marfanoid disorder with craniosynostosis type 1', 'Marfanoid disorder with craniosynostosis, type 1', 'Marfanoid-craniosynostosis syndrome']",,182212,2462,C1321551,"['-0.2761', '0.05557', '0.3633', '-0.1924', '0.1531', '-0.3345', '-0.1068', '0.5566', '-0.2617', '-0.10986', '-0.1699', '-0.11224', '0.1655', '0.03117', '-0.2112', '0.04318', '0.10443', '0.00803', '-0.318', '-0.581', '0.1051', '0.1382', '0.238', '-0.3777', '0.3123', '0.1488', '0.02322', '0.0615', '0.5303', '-0.1616', '0.1772', '-0.1119', '0.499', '0.3303', '0.006298', '0.09595', '-0.0997', '-0.2341', '-0.1836', '-0.4604', '0.08826', '-0.1234', '0.1146', '-0.2388', '0.305', '-0.1611', '-0.03836', '0.2546', '-0.2148', '-0.1338', '-0.2076', '0.1196', '-0.125', '-0.0834', '-0.2325', '-0.08307', '-0.08453', '0.10266', '-0.0796', '0.2705', '0.4966', '-0.11505', '-0.1257', '0.006474', '0.11285', '-0.0612', '0.1436', '0.08307', '-0.338', '0.2174', '-0.4998', '0.074', '0.03778', '-0.06055', '-0.3127', '0.109', '0.0837', '-0.0665', '-0.302', '-0.3147', '0.1991', '-0.005096', '-0.3381', '0.3555', '0.0427', '0.05106', '-0.02586', '0.416', '0.2507', '0.163', '-0.1058', '0.3262', '0.156', '0.2202', '0.4539', '-0.00944', '0.458', '-0.1632', '0.458', '0.1357']",C124840,,,,,,
mondo:0008427,"sister chromatid exchange, frequency of","['SCE, frequency of', 'sister chromatid exchange, frequency of']",,182220,,,,,,,,,,
mondo:0008428,septooptic dysplasia,"['hypopituitarism and septooptic ^dysplasia^', 'pituitary hormone deficiency, combined, 5', 'septo-optic dysplasia sequence', 'septo-optic dysplasia with growth hormone deficiency', 'SOD', 'septooptic dysplasia', 'septo-optic dysplasia spectrum', 'Growth hormone deficiency with pituitary anomalies', 'septo-optic dysplasia', 'De Morsier syndrome']",0060857,182230,3157,C0338503,"['-0.0661', '0.1747', '0.4395', '-0.3005', '0.4148', '0.486', '0.3647', '0.9023', '-0.1885', '-0.7144', '-0.2644', '-0.7', '-0.03638', '0.3496', '-0.06085', '-0.6533', '0.0756', '-0.321', '-0.4944', '-0.4436', '0.0672', '-0.2053', '0.5483', '-0.3474', '-0.1696', '-0.2969', '-0.2023', '-0.2576', '0.3745', '0.02867', '0.648', '-0.06537', '0.6646', '0.5986', '-0.1793', '0.1256', '0.1887', '-0.498', '-0.378', '0.04724', '0.1631', '0.2039', '0.3586', '-0.10956', '0.3794', '-0.351', '-0.01371', '0.1244', '0.02277', '0.3713', '0.47', '-0.004166', '-0.5117', '-0.09564', '0.013916', '0.3984', '0.2035', '-0.6094', '-0.0317', '0.4666', '-0.0779', '0.3604', '0.2128', '0.05264', '-0.7354', '0.3018', '0.1083', '0.4312', '-0.2944', '0.0379', '0.09076', '0.4202', '-0.1749', '0.1503', '0.6294', '-0.375', '0.4192', '-0.328', '-0.3818', '-0.2737', '0.2988', '-0.06134', '-0.1584', '0.623', '-0.3062', '-0.02898', '0.176', '0.4348', '0.3762', '0.1958', '0.631', '0.3801', '-0.02731', '-0.3062', '0.682', '-0.7515', '0.3613', '-0.0412', '0.2866', '0.5117']",C85063,,D025962,,,10067159,
mondo:0008429,Singleton-Merten dysplasia,"['singleton Merten syndrome', 'syndrome of widened medullary cavities of the metacarpals and phalanges, aortic calcification and abnormal dentition', 'Merten-Singleton syndrome', 'SGMRT1', 'widened medullary cavities of bone, aortic calcification, abnormal dentition, and muscular weakness', 'Singleton-Merten syndrome', 'SM syndrome']",,,85191,C0432254,"['-0.3386', '0.1124', '0.0991', '-0.2568', '0.2029', '-0.4136', '-0.1346', '0.4324', '-0.184', '-0.04013', '-0.233', '-0.1824', '-0.0458', '0.002308', '0.07434', '0.0914', '-0.1176', '0.05273', '-0.3472', '-0.2274', '0.0506', '0.04697', '0.2351', '-0.3406', '0.03897', '-0.0894', '-0.1699', '0.1832', '-0.04562', '-0.2551', '0.2339', '-0.321', '0.1901', '-0.1506', '0.2332', '-0.271', '-0.1858', '-0.213', '-0.1648', '-0.272', '0.1069', '-0.2869', '-0.04703', '-0.1818', '-0.0982', '-0.01741', '-0.2441', '0.2732', '-0.3135', '-0.2617', '-0.1493', '-0.01677', '0.329', '0.5474', '-0.12054', '-0.55', '0.3145', '-0.127', '-0.1704', '-0.0803', '0.3748', '-0.0647', '-0.2041', '0.011856', '-0.2532', '-0.2386', '0.2915', '0.3792', '-0.2976', '0.4001', '-0.02771', '-0.2281', '0.045', '0.02689', '-0.248', '0.1039', '-0.2966', '0.1185', '0.04327', '-0.3528', '0.1621', '0.3354', '0.2393', '0.1034', '-0.2278', '0.248', '0.12134', '0.3076', '0.00512', '-0.3174', '-0.0642', '0.2302', '0.1893', '0.11096', '0.603', '-0.04785', '0.4006', '-0.08', '-0.05093', '-0.04263']",,,C537343,733.29,,,
mondo:0008430,skeletal dysplasia with delayed epiphyseal and carpal bone ossification,['skeletal dysplasia with delayed epiphyseal and carpal bone ossification'],,182255,,C1866939,,,,C566687,,,,
mondo:0008431,slipped femoral capital epiphyses,"['epiphysiolysis capitis femoris', 'slipped femoral capital epiphyses']",,182260,,C0149887,,,,D060048,,,,
mondo:0008433,small cell lung carcinoma,"['lung small cell carcinoma', 'oat cell lung carcinoma', 'small-cell cancer of lung', 'SCLC', 'small cell carcinoma of lung', 'small cell neuroendocrine carcinoma of the lung', 'lung small cell neuroendocrine carcinoma', 'poorly differentiated endocrine neoplasm', 'lung oat cell carcinoma', 'SCLC1', 'small cell cancer of the lung', 'small cell cancer of the lung, somatic', 'oat cell carcinoma (morphologic abnormality)', 'oat cell carcinoma', 'small cell carcinoma of the lung', 'small cell lung cancer', 'oat cell carcinoma of the lung', 'small cell neuroendocrine carcinoma of lung', 'oat cell carcinoma of lung']",5411,182280,70573,CN244903,,C4917,0000702,D055752,162.9,,,
mondo:0008434,Smith-Magenis syndrome,"['Smith-Magenis chromosome region', 'chromosome 17p11.2 deletion syndrome', 'Smith-Magenis syndrome', 'Smith-Magenis syndrome chromosome region', 'SMS', '17p11.2 microdeletion syndrome', 'SMITH-Magenis syndrome', 'Smith-Magenis syndrome, Isolated cases', 'chromosome 17P11.2 deletion syndrome']",0060768,182290,819,C0795864,"['-0.04626', '0.289', '0.1302', '-0.001866', '-0.4895', '-0.088', '0.6094', '0.8677', '-0.3464', '-0.2527', '0.11816', '-0.2166', '0.1932', '0.1125', '0.1305', '0.1884', '-0.02509', '-0.1936', '-0.586', '-0.2825', '0.2097', '0.293', '0.421', '0.4497', '-0.0165', '-0.4604', '-0.002094', '0.04922', '0.3945', '-0.1415', '0.994', '-0.3245', '0.9106', '0.09674', '0.1072', '-0.3376', '-0.4504', '-0.613', '-0.04352', '-0.784', '0.5923', '0.2156', '0.1902', '0.11755', '0.83', '-0.3901', '0.1492', '-0.1707', '-0.1299', '0.6714', '-0.5586', '0.732', '-0.6104', '-0.086', '-0.1885', '-0.3296', '0.0941', '-0.639', '-0.03555', '-0.1288', '0.3062', '-0.1493', '-0.11786', '-0.0669', '-0.058', '0.0509', '-0.1638', '0.101', '-0.355', '-0.11566', '-0.7', '-0.1146', '-0.709', '0.2927', '-0.0682', '-0.1566', '0.2515', '-0.2489', '-0.2368', '-0.323', '0.271', '-0.4893', '0.2795', '1.1', '0.287', '0.523', '-0.3525', '-0.12476', '-0.03177', '0.439', '0.06107', '0.5513', '-0.669', '-0.13', '0.693', '-0.1251', '0.431', '-0.8027', '0.3213', '0.511']",C75469,,D058496,758.33,,,
mondo:0008435,"Somatomedin, embryonic","['Somatomedin, embryonic']",,182400,,,,,,,,,,
mondo:0008436,Sneddon syndrome,"['livedo racemosa and cerebrovascular accidents', 'livedo reticularis and cerebrovascular accidents', 'Sneddon^s syndrome', 'Ehrmann-Sneddon syndrome', 'Sneddon syndrome', 'livedo reticularis-cerebrovascular accident syndrome', 'livedo racemosa-cerebrovascular accident syndrome', 'idiopathic livedo reticularis with systemic involvement', 'cerebro-vascular lesions and livedo reticularis']",13096,182410,820,C0282492,"['-0.004772', '-0.1696', '-0.304', '-0.4094', '-0.0487', '-0.3333', '0.63', '0.10626', '-0.3706', '0.11694', '-0.2108', '0.0916', '-0.08246', '-0.212', '0.1757', '-0.2554', '-0.3135', '-0.119', '0.2416', '-0.0914', '-0.3315', '-0.3425', '-0.5034', '-0.4856', '-0.703', '-0.5586', '-0.175', '0.1857', '-0.128', '-0.1234', '0.791', '-0.1987', '0.94', '0.2815', '0.6274', '-0.2861', '0.0711', '-0.3127', '0.3738', '-0.3535', '0.3389', '-0.324', '0.942', '-0.279', '0.531', '0.3833', '-0.2172', '0.04437', '-0.0417', '0.2935', '-0.00874', '0.3513', '0.0639', '0.2844', '-0.09467', '0.308', '0.6724', '-0.618', '-0.5977', '0.011894', '-0.1088', '0.3752', '0.06247', '-0.3696', '-0.0714', '-0.1671', '0.01533', '0.4197', '0.2184', '0.4448', '-0.2668', '-0.6523', '-0.356', '0.1045', '0.4832', '0.4968', '0.57', '0.522', '0.05655', '-0.4792', '0.264', '0.1007', '0.358', '0.1644', '0.3381', '0.459', '0.3306', '0.505', '0.2344', '0.0559', '0.547', '0.03983', '-0.00494', '-0.2834', '0.5024', '-0.3186', '0.392', '-0.3428', '-0.1203', '-0.03986']",,1001186,D018860,,,10053841,
mondo:0008437,hereditary spastic paraplegia 3A,"['Spg3', 'hereditary spastic paraplegia caused by mutation in ATL1', 'spastic paraplegia 3, autosomal dominant', 'autosomal dominant familial spastic paraplegia 1', 'autosomal dominant spastic paraplegia 3', 'strumpell disease', 'ATL1 hereditary spastic paraplegia', 'SPG3A', 'Strumpell disease', 'familial spastic paraplegia, autosomal dominant, 1', 'hereditary spastic paraplegia type 3A', 'spastic paraplegia 3a, autosomal dominant', 'spastic paraplegia 3', 'Strümpell disease', 'spastic Paraplegia 3A', 'autosomal dominant spastic paraplegia type 3', 'FSP1']",0110791,182600,100984,C2931355,"['-0.1293', '0.2173', '0.216', '-0.4573', '-0.1841', '-0.5713', '-0.2998', '0.2241', '-0.882', '-0.01145', '-0.03076', '0.04547', '-0.1335', '-0.0265', '0.33', '-0.0689', '0.00973', '-0.1716', '0.0133', '-0.5283', '0.1581', '-0.006428', '-0.1349', '0.2137', '0.1879', '0.2013', '0.04373', '-0.005062', '-0.1159', '-0.286', '0.06097', '-0.08734', '-0.05518', '0.2474', '-0.1772', '-0.5005', '-0.2369', '0.02983', '-0.2502', '-0.1973', '0.2196', '-0.313', '-0.1742', '0.1549', '-0.04956', '-0.4424', '-0.1831', '0.05966', '-0.049', '0.2172', '-0.0972', '0.1992', '-0.2163', '-0.4897', '0.0343', '-0.279', '0.336', '-0.1715', '-0.3918', '0.1173', '-0.072', '-0.004642', '0.5684', '0.2715', '-0.2222', '0.5103', '0.2676', '0.5005', '-0.3076', '0.2417', '-0.4177', '0.2664', '0.1465', '-0.2842', '0.5664', '0.02922', '0.0905', '0.2856', '0.082', '-0.2666', '0.05704', '-0.254', '0.4897', '0.6963', '-0.193', '0.18', '-0.11084', '0.3196', '0.0876', '0.1838', '0.1362', '0.2279', '0.1868', '-0.1556', '0.778', '0.1838', '0.6465', '0.004375', '0.04984', '0.2605']",C142893,,C536864,,,,
mondo:0008438,hereditary spastic paraplegia 4,"['familial spastic paraplegia, autosomal dominant, 2', 'spastic paraplegia 4, autosomal dominant', 'familial spastic paraplegia autosomal dominant 2', 'spastic paraplegia 4', 'autosomal dominant spastic paraplegia type 4', 'hereditary spastic paraplegia caused by mutation in SPAST', 'autosomal dominant spastic paraplegia 4', 'SPG4', 'hereditary spastic paraplegia type 4', 'FSP2', 'SPAST hereditary spastic paraplegia']",0110792,182601,100985,C4510079,"['-0.0949', '-0.11035', '-0.1824', '0.1', '-0.557', '-0.9897', '-0.2651', '1.132', '-0.9443', '-0.791', '0.03705', '0.1917', '-0.3765', '0.1942', '0.4897', '-0.3794', '-0.1917', '-0.4543', '0.3213', '-0.5566', '0.2112', '-0.0924', '0.0828', '0.0489', '0.4165', '0.3105', '-0.014206', '0.04062', '-0.1117', '-0.05756', '0.0723', '-0.2769', '0.1425', '0.4314', '-0.09674', '-0.4182', '-0.529', '0.00412', '-0.07385', '-0.128', '-0.156', '-0.9077', '0.6333', '0.04715', '0.1538', '-0.704', '-0.1691', '-0.11755', '0.014305', '-0.006134', '0.371', '1.081', '-0.701', '-0.3506', '-0.1143', '-0.216', '0.653', '-0.6255', '0.2676', '-0.1299', '0.0005007', '0.0725', '0.3274', '-0.1626', '-0.3135', '0.2534', '0.172', '0.772', '0.02931', '0.1383', '-0.011925', '0.4204', '0.2803', '0.221', '0.7725', '0.2976', '0.00823', '-0.1483', '-0.0698', '0.2524', '-0.3542', '0.02873', '0.5225', '0.8223', '0.1803', '0.07825', '-0.1354', '0.1037', '0.48', '-0.1307', '0.507', '0.5044', '0.3462', '-0.2578', '0.8677', '0.67', '0.965', '-0.119', '-0.0718', '-0.403']",C129981,,C536865,,,,
mondo:0008439,spastic paraplegia-epilepsy-intellectual disability syndrome,"['spastic paraplegia, epilepsy, and mental retardation', 'spemr', 'spastic paraplegia, epilepsy, and intellectual disability', 'spastic paraplegia epilepsy intellectual disability', 'SPEMR', 'spastic paraplegia epilepsy mental retardation']",,182610,2816,C1866854,,,,C536869,,,,
mondo:0008440,spastic paraplegia-nephritis-deafness syndrome,"['spastic paraplegia - nephritis - deafness', 'spastic paraplegia, sensorineural deafness, mental retardation, and progressive nephropathy', 'spastic paraplegia, bilateral sensorineural deafness, intellectual retardation, and progressive nephropathy', 'Fitzsimmons Walson Mellor syndrome', 'Fitzsimmons-Walson-Mellor syndrome', 'spastic paraplegia, sensorineural deafness, intellectual disability, and progressive nephropathy']",,182690,2820,C2931667,,,,C537937,,,,
mondo:0008441,spastic paraplegia with associated extrapyramidal signs,['spastic paraplegia with associated extrapyramidal signs'],,182800,,C1866852,,,,C566681,,,,
mondo:0008442,spastic paraplegia-neuropathy-poikiloderma syndrome,"['spastic paraplegia with neuropathy and poikiloderma', 'familial spastic paraplegia with neuropathy and poikiloderma', 'Antinolo-Nieto-Borrego syndrome', 'spastic paraplegia neuropathy poikiloderma']",,182815,2821,C1866851,,,,C536870,,,,
mondo:0008443,spastic paraplegia-precocious puberty syndrome,"['familial spastic paraplegia, intellectual disability, and precocious puberty', 'spastic paraplegia with precocious puberty', 'familial spastic paraplegia, mental retardation, and precocious puberty', 'precocious puberty with spastic paraplegia']",,182820,2826,C1866850,,,,C536874,,,,
mondo:0008444,"spastic paraplegia, optic atrophy, and dementia","['spastic paraplegia, optic atrophy, and dementia']",,182830,,C1866849,,,,C566679,,,,
mondo:0008445,delayed speech-facial asymmetry-strabismus-ear lobe creases syndrome,"['Mehes syndrome', 'speech development, delayed, with facial asymmetry, strabismus, and transverse earlobe CREASE', 'delayed speech development, facial asymmetry, strabismus, and transverse ear lobe creases']",,182875,3038,C2931119,,,,,,,,
mondo:0008446,sperm protamine P4,"['sperm protamine P4', 'PRM4']",,182882,,,,,,,,,,
mondo:0008447,hereditary spherocytosis type 1,"['HS1', 'spherocytosis, hereditary, 1', 'hereditary spherocytosis caused by mutation in ANK1', 'hereditary spherocytosis 1', 'SPH1', 'Sph', 'spherocytosis, type 1', 'ANK1 hereditary spherocytosis']",0110916,182900,,C2674218,,,,,,,,
mondo:0008449,spina bifida,"['spina bifida (disease)', 'spinal myelomeningocele', 'NTD', 'rachischisis', 'spina bifida', 'neural tube defects, susceptibility to', 'spinal myelocele', 'spinal meningocele']",0080016,,,,"['-0.005154', '0.02933', '-0.0911', '-0.0411', '0.608', '-0.161', '-0.332', '0.531', '-0.932', '0.1316', '-0.0831', '-0.0747', '-0.406', '0.8857', '-0.53', '-0.358', '-0.603', '-0.4968', '-0.283', '-0.7837', '-0.2612', '-0.5127', '0.0554', '0.2324', '-0.4028', '-0.6455', '0.04373', '-0.1109', '0.2722', '0.1772', '0.2534', '-0.5337', '0.4595', '-0.1037', '-0.1431', '0.10345', '0.1866', '0.3293', '0.746', '-0.3152', '0.11835', '-0.1302', '0.0714', '0.1597', '-0.502', '-0.2583', '0.1846', '-0.2922', '-0.311', '-0.003666', '-0.5527', '-0.3184', '-0.01617', '-0.6636', '-0.967', '0.4502', '-0.362', '0.6406', '0.2408', '0.02249', '-0.4048', '-0.186', '-0.2976', '0.619', '0.09845', '0.7036', '0.4617', '0.256', '-0.00679', '1.078', '0.095', '0.5312', '-0.5244', '-0.769', '-0.2544', '0.2676', '0.1915', '0.05045', '0.3564', '0.1278', '-0.7627', '0.0674', '-0.1996', '0.2822', '0.3923', '0.5073', '-0.2563', '0.06866', '0.487', '0.2394', '-0.3345', '0.5073', '0.07776', '0.3005', '0.5874', '-0.1327', '0.2656', '-0.2964', '0.09033', '0.08514']",C101214,0003105,D016135,741,,,0002414
mondo:0008450,spinal arachnoiditis,"['spinal arachnoiditis', 'arachnoiditis, spinal']",,182950,,C1710146,,C50749,,C531624,,,,
mondo:0008451,"neuronopathy, distal hereditary motor, type 1","['neuronopathy, distal hereditary motor, type I', 'dHMN1', 'HMN1', 'autosomal dominant distal juvenile spinal muscular atrophy type 1', 'neuropathy, distal hereditary motor, type 1', 'HMN 1', 'distal hereditary motor neuronopathy type I', 'Charcot-Marie-Tooth disease, spinal, 1', 'Charcot-Marie-Tooth disease, spinal, I', 'spinal muscular atrophy, distal, juvenile, autosomal dominant, 1']",0111200,182960,139518,C1866784,,C132826,,C566675,,,,
mondo:0008452,"spinal muscular atrophy, facioscapulohumeral type","['spinal muscular atrophy, facioscapulohumeral type', 'Fshsma']",,182970,,C1866783,,,,C566674,,,,
mondo:0008453,"adult-onset proximal spinal muscular atrophy, autosomal dominant","['autosomal dominant adult-onset proximal SMA', 'Finkel disease', 'autosomal dominant late-onset spinal muscular atrophy, Finkel type', 'spinal muscular atrophy, proximal, adult, autosomal dominant', 'spinal muscular atrophy, late-onset, FINKEL type', 'autosomal dominant adult-onset proximal spinal muscular atrophy', 'Finkel late-adult type Sma', 'SMAFK']",0111194,182980,209335,CN200940,"['-0.22', '0.1172', '0.1829', '-0.307', '-0.06235', '-0.428', '0.0599', '0.4', '-0.5527', '0.01343', '-0.1304', '-0.02342', '-0.2654', '-0.0707', '0.2915', '-0.02351', '0.05228', '-0.2384', '-0.0399', '-0.5376', '-0.01894', '-0.1697', '0.04462', '0.2042', '-0.07446', '0.02559', '0.1588', '-0.2134', '-0.3616', '-0.1837', '0.01909', '0.162', '0.1898', '0.00885', '0.01409', '-0.1497', '-0.2593', '0.05814', '0.053', '-0.2101', '-0.1597', '-0.3762', '-0.0911', '0.3176', '-0.1794', '-0.1554', '-0.1833', '0.2766', '-0.0632', '0.1279', '-0.07935', '0.2029', '-0.08136', '-0.2018', '0.005592', '-0.4087', '0.2544', '-0.1582', '-0.3428', '-0.0426', '0.1164', '0.02342', '0.07904', '0.0254', '-0.354', '0.0429', '0.282', '0.3984', '-0.137', '0.1484', '-0.284', '-0.12103', '0.1302', '-0.2019', '0.4028', '0.0983', '-0.01636', '0.1075', '-0.06058', '-0.154', '0.07446', '-0.1649', '0.162', '0.4336', '-0.08997', '0.1656', '-0.0511', '0.2428', '0.2103', '-0.1412', '0.2196', '0.1779', '0.1757', '0.2407', '0.3894', '0.08685', '0.505', '0.008934', '-0.1226', '0.2408']",,,,,,,
mondo:0008454,spinal intradural arachnoid cysts,"['spinal intradural arachnoid cysts', 'arachnoid cysts, spinal intradural']",,182990,,,,,,C536878,,,,
mondo:0008455,"spinal muscular atrophy, segmental","['spinal muscular atrophy, segmental']",,183020,,C1866774,,,,C566670,,,,
mondo:0008456,spinocerebellar ataxia with rigidity and peripheral neuropathy,['spinocerebellar ataxia with rigidity and peripheral neuropathy'],,183050,,C1866770,,,,C566669,,,,
mondo:0008457,spinocerebellar ataxia type 6,"['spinocerebellar ataxia type 6', 'spinocerebellar ataxia 6', 'SCA6', 'autosomal dominant cerebellar ataxia type III caused by mutation in CACNA1A', 'CACNA1A autosomal dominant cerebellar ataxia type III']",0050956,183086,98758,C0752124,"['0.000769', '-0.1416', '-0.0321', '0.0941', '0.05865', '-0.6353', '0.4285', '0.3965', '-0.635', '-0.7593', '0.08997', '0.2888', '-0.2283', '0.2468', '0.6973', '-0.4612', '-0.2284', '-0.3083', '0.1366', '-0.8647', '-0.2208', '-0.4324', '0.03308', '-0.3892', '-0.0363', '-0.6655', '-0.2115', '0.133', '0.09174', '-0.7773', '0.1986', '0.2551', '-0.3533', '-0.2063', '0.2603', '0.089', '0.0456', '0.168', '0.4163', '0.4302', '0.4714', '0.11566', '-0.2308', '0.545', '0.5283', '-0.6934', '-0.05957', '0.2395', '0.4314', '-0.1377', '-0.2108', '0.04654', '-0.02632', '-0.4924', '-0.10016', '-0.4807', '0.49', '0.5894', '-0.1616', '0.3682', '-0.3918', '0.3608', '0.1697', '-0.1908', '-0.348', '0.4465', '0.2668', '0.3306', '-0.636', '0.4014', '0.602', '0.3506', '-0.2343', '-0.862', '0.774', '0.2637', '0.2798', '0.08997', '0.0956', '0.3967', '-0.1661', '-0.9844', '0.4707', '0.648', '-0.11096', '-0.5815', '0.1022', '-0.03099', '0.6724', '0.3037', '0.2097', '0.3772', '-0.0711', '-0.1586', '0.8975', '1.025', '0.3943', '0.576', '-0.2888', '-0.0919']",C142838,,,,,,
mondo:0008458,spinocerebellar ataxia type 2,"['SCA2', 'spinocerebellar ataxia Cuban type', 'Wadia swami syndrome', 'spinocerebellar ataxia with slow eye movements', 'amyotrophic lateral sclerosis, susceptibility to, 13', 'ATXN2 autosomal dominant cerebellar ataxia type I', 'spinocerebellar ataxia 2', 'OPCA2', 'SCA 2', 'Wadia-swami syndrome', 'amyotrophic lateral sclerosis 13', 'spinocerebellar atrophy 2', 'cerebellar Degeneration with slow eye movements', 'olivopontocerebellar atrophy, Holguin type', 'amyotrophic lateral sclerosis type 13', 'olivopontocerebellar atrophy 2', 'ALS13', 'spinocerebellar Degeneration with slow eye movements', 'spinocerebellar ataxia type 2', 'spinocerebellar ataxia, Cuban type', 'autosomal dominant cerebellar ataxia type I caused by mutation in ATXN2', 'olivopontocerebellar atrophy Holguin type']",0060204,183090,98756,C0752121,"['-0.0955', '-0.1576', '-0.04794', '0.1', '-0.1772', '-0.886', '0.1244', '0.1478', '-0.3992', '-0.9116', '0.02058', '0.2793', '-0.1403', '0.06555', '0.68', '-0.2466', '-0.21', '-0.2183', '0.3494', '-0.8584', '-0.11993', '-0.4988', '0.3384', '-0.388', '0.2278', '-0.225', '-0.3074', '0.0627', '-0.03647', '-0.9976', '0.1238', '0.2292', '-0.532', '-0.0798', '0.3093', '0.0716', '-0.06097', '0.2302', '0.5093', '0.444', '0.3818', '0.1957', '-0.259', '0.3975', '0.4136', '-0.589', '0.1978', '0.4893', '0.44', '-0.1022', '-0.02948', '0.1837', '-0.1191', '-0.4985', '0.05222', '-0.545', '0.3801', '0.6206', '-0.05978', '0.2898', '-0.4783', '0.294', '0.2551', '-0.05753', '-0.2644', '0.4207', '0.0143', '0.4124', '-0.4968', '0.2805', '0.8423', '0.4392', '-0.02559', '-0.8486', '0.6265', '0.2068', '0.3333', '0.3362', '-0.0439', '0.2194', '-0.1183', '-0.9473', '0.338', '0.6445', '-0.2167', '-0.6', '0.3008', '-0.04712', '0.7456', '0.414', '0.3936', '0.463', '0.1619', '0.01971', '1.063', '0.886', '0.4077', '0.3542', '-0.158', '0.0703']",C148315,,,,,,
mondo:0008459,spinocerebellar atrophy with pupillary paralysis,['spinocerebellar atrophy with pupillary paralysis'],,183100,,C1866746,,,,C566668,,,,
mondo:0008460,splenogonadal fusion-limb defects-micrognathia syndrome,"['splenogonadal fusion limb defect syndrome', 'splenogonadal fusion limb defects micrognatia', 'SGFLD syndrome', 'splenogonadal fusion limb defects syndrome', 'splenogonadal fusion with limb defects and micrognathia', 'Sgfld syndrome']",,183300,2063,C1866745,,,,C537318,,,,
mondo:0008461,splenomegaly syndrome with splenic Germinal center hypoplasia and reduced circulating T helper cells,['splenomegaly syndrome with splenic Germinal center hypoplasia and reduced circulating T helper cells'],,183350,,C1866744,,,,C566666,,,,
mondo:0008462,split lower lip,"['split lower lip', 'split Lower type lip']",,183400,,,,,,,,,,
mondo:0008463,split-hand and split-foot with hypodontia,['split-hand and split-foot with hypodontia'],,183500,,C1866742,,,,C566665,,,,
mondo:0008464,split hand-foot malformation 1,"['ectrodactyly', 'split-hand deformity', 'split-hand/foot deformity 1', 'split-hand/foot malformation 1 with or without deafness', 'split hand/foot malformation 1', 'SHFM1', 'split-hand/foot malformation type 1', 'split-hand/foot malformation 1', 'SHFD1', 'split hand-foot malformation type 1']",0090021,183600,,C2931019,,C75045,,,,,,
mondo:0008465,Patterson-Stevenson-Fontaine syndrome,"['Patterson-Stevenson-Fontaine syndrome', 'Patterson-Stevenson syndrome', 'split-foot deformity with mandibulofacial dysostosis', 'split foot deformity-mandibulofacial dysostosis syndrome', 'Patterson Stevenson Fontaine syndrome', 'split-foot deformity with ectrodactyly and mandibulofacial dysostosis']",,183700,2439,C1866741,,,,,,,,
mondo:0008466,Karsch-Neugebauer syndrome,"['Karsch-Neugebauer syndrome', 'split-hand with congenital NYSTAGMUS, fundal changes, and cataracts', 'split hand nystagmus syndrome', 'split hand split foot nystagmus', 'KNS', 'Nystagmus-split hand syndrome', 'split hand/split foot-nystagmus syndrome']",,183800,2329,C1866740,,,,C537319,,,,
mondo:0008467,Czeizel-Losonci syndrome,"['split hand urinary anomalies spina bifida', 'split hand-urinary anomalies-spina bifida syndrome', 'split hand with obstructive uropathy, spina bifida and diaphragmatic defects', 'split-hand with obstructive uropathy, spina bifida, and diaphragmatic defects']",,183802,2437,C1866739,,,,C566662,,,,
mondo:0008468,"spondyloarthropathy, susceptibility to, 2","['SPDA2', 'spondyloarthropathy, susceptibility to, 2']",0080604,183840,,C1866738,,,,,,,,
mondo:0008469,spondyloepimetaphyseal dysplasia-hypotrichosis syndrome,"['Whyte syndrome', 'Whyte Petersen McAlister syndrome', 'spondyloepimetaphyseal dysplasia with hypotrichosis']",,183849,168443,C1866728,,,,C535783,,,,
mondo:0008470,spondyloepiphyseal dysplasia with punctate corneal dystrophy,"['spondyloepiphyseal dysplasia with punctate corneal dystrophy', 'spondyloepiphyseal dysplasia, Byers type']",0112286,183850,163673,C1866727,,,,C566660,,,,
mondo:0008471,spondyloepiphyseal dysplasia congenita,"['spondyloepiphyseal dysplasia congenita', 'SEDC', 'spondyloepiphyseal dysplasia, congenital type', 'Spranger-Wiedemann disease', 'SED congenita', 'congenital spondyloepiphyseal dysplasia']",14789,183900,94068,,"['-0.6743', '0.3633', '-0.0725', '-0.2905', '0.2546', '-0.13', '0.02379', '0.952', '-0.443', '-0.2852', '0.2307', '-0.11993', '-0.07825', '0.3071', '0.01508', '0.2347', '0.572', '-0.01159', '-0.2607', '-0.4155', '-0.5444', '-0.0952', '0.527', '0.07605', '0.08997', '0.2177', '-0.1901', '-0.1359', '0.2488', '0.1666', '0.3984', '-0.572', '0.29', '0.1636', '-0.01152', '0.36', '0.07355', '-0.582', '-0.01588', '0.03049', '0.088', '0.0512', '-0.2349', '0.03943', '-0.0004954', '-0.0413', '-0.02434', '0.3582', '0.2148', '-0.03632', '0.0879', '0.01733', '-0.05145', '-0.185', '-0.1871', '-0.4521', '0.1321', '-0.663', '0.03976', '-0.1951', '0.4688', '-0.1478', '-0.5435', '0.523', '-0.1268', '-0.1359', '0.456', '0.4365', '-0.0888', '0.5283', '-0.298', '0.148', '-0.0787', '-0.3804', '-0.1203', '0.2617', '-0.3215', '-0.1372', '-0.441', '-0.3684', '0.05103', '-0.2308', '0.1353', '0.4358', '-0.4255', '0.1464', '-0.01178', '0.04285', '0.1807', '0.432', '-0.2396', '-0.01208', '0.08075', '0.3474', '0.4836', '-0.06934', '0.6445', '0.06946', '0.11957', '0.1094']",,,C535788,756.9,Q77.7,10062920,
mondo:0008472,"spondyloepiphyseal dysplasia, MacDermot type","['spondyloepiphyseal dysplasia, myopia, and sensorineural deafness', 'spondyloepiphyseal dysplasia-myopia-sensorineural deafness syndrome']",,184000,163668,C1866719,,,,C566659,,,,
mondo:0008473,"spondyloepimetaphyseal dysplasia, Maroteaux type","['pseudo-Morquio syndrome type 2', 'spondyloepiphyseal dysplasia Maroteaux type', 'SED, Maroteaux type', 'spondyloepiphyseal dysplasia, Maroteaux type', 'brachyolmia Maroteaux type', 'spondyloepimetaphyseal dysplasia, Maroteaux type', 'pseudo-Morquio syndrome, type 2']",0111553,184095,263482,CN202294,"['-0.573', '0.5444', '0.1777', '-0.419', '0.3662', '-0.5967', '-0.297', '0.96', '-0.393', '-0.504', '0.02335', '-0.03995', '-0.445', '0.0167', '-0.1622', '0.3005', '0.9224', '-0.07477', '0.0748', '-0.4011', '-0.2734', '-0.238', '0.3818', '-0.2451', '-0.225', '0.3142', '0.0864', '-0.1738', '0.297', '-0.3003', '0.01733', '-0.3735', '0.299', '0.4114', '0.05737', '-0.438', '-0.521', '-0.5396', '-0.0159', '0.0714', '-0.2556', '-0.3364', '-0.02402', '0.1029', '-0.1833', '-0.3289', '-0.3066', '0.8613', '0.271', '-0.3584', '0.3594', '0.129', '-0.1632', '0.2808', '-0.5166', '-0.793', '-0.2126', '-0.586', '0.1091', '0.019', '0.4446', '0.282', '-0.563', '-0.01377', '-0.3015', '0.03613', '0.423', '0.753', '-0.5957', '0.343', '0.08997', '-0.06323', '0.2888', '-0.2178', '-0.1844', '0.642', '-1.102', '0.4036', '-0.3794', '-0.08203', '-0.06506', '0.1309', '0.2494', '-0.2798', '0.001228', '0.3647', '0.0206', '0.07465', '0.779', '-0.05978', '-0.03757', '0.2019', '-0.2793', '0.213', '0.9404', '0.2803', '0.3826', '-0.3918', '0.4077', '0.2563']",,,,,,,
mondo:0008474,"spondyloepiphyseal dysplasia tarda, autosomal dominant","['spondyloepiphyseal dysplasia tarda, autosomal dominant']",0112285,184100,,C1866717,,,,C566658,,,,
mondo:0008475,spondylolisthesis,"['spondylolisthesis', 'spondylolisthesis (disease)']",6682,184200,,C0038016,,C35033,0007493,D013168,,,,0003302
mondo:0008476,"spondyloepimetaphyseal dysplasia, Strudwick type","['SEMD, Strudwick type', 'SMED type 1', 'SmD', 'Strudwick syndrome', 'spondylometaphyseal dysplasia', 'spondyloepimetaphyseal dysplasia congenita, Strudwick type', 'spondylometaepiphyseal dysplasia congenita, Strudwick type', 'SEMDSTWK', 'SMED Strudwick type', 'Smed, Strudwick type', 'dappled metaphysis syndrome', 'spondyloepimetaphyseal dysplasia, Strudwick type', 'Semdc', 'spondyloepimetaphyseal dysplasia Strudwick type', 'Smed, type 1']",0080028,184250,93346,,"['-0.3752', '0.1929', '-0.03802', '-0.01743', '0.4194', '-0.8', '-0.2228', '0.4343', '-0.694', '-0.3457', '-0.362', '-0.0632', '-0.0509', '0.1346', '0.04166', '0.1646', '0.3677', '-0.03912', '-0.2267', '-0.5947', '-0.1152', '0.2654', '0.344', '-0.1681', '-0.05032', '0.2605', '-0.05356', '-0.02328', '0.2812', '-0.0749', '0.1528', '-0.4224', '0.0802', '0.353', '0.4316', '0.2206', '-0.2261', '-0.6416', '-0.0825', '0.2347', '-0.09033', '-0.2367', '-0.11694', '0.3445', '0.0516', '0.02931', '-0.343', '0.503', '0.1377', '-0.1451', '0.4426', '0.0792', '-0.0658', '0.0946', '0.088', '-0.765', '-0.2178', '-0.2942', '0.0854', '0.1743', '0.4412', '-0.08954', '-0.5464', '0.31', '-0.3904', '-0.2922', '0.4285', '0.5664', '-0.3862', '0.4788', '0.1046', '-0.1633', '-0.01675', '-0.2961', '0.1768', '0.0417', '-0.3743', '0.102', '-0.1449', '-0.3083', '-0.028', '0.2722', '0.11115', '0.7183', '-0.2866', '0.2428', '0.0756', '0.4265', '0.1144', '0.4949', '-0.087', '0.01822', '0.1122', '0.3088', '0.624', '0.1769', '0.837', '-0.262', '0.3662', '0.1543']",,,,758.89,,,
mondo:0008477,"spondylometaphyseal dysplasia, Kozlowski type","['spondylometaphyseal dysplasia, Kozlowski type', 'SmD Kozlowski type', 'SmD, Kozlowski type', 'skeletal dysplasia Jequier-Kozlowski type', 'Jequier Kozlowski skeletal dysplasia', 'SMDK', 'Dysmorphism arthrogryposis skeletal maturation advanced', 'Jequier-Kozlowski syndrome']",0111554,184252,93314,,"['-0.295', '0.4094', '0.1316', '-0.504', '0.4668', '-0.414', '0.1404', '0.674', '-0.786', '-0.325', '0.2598', '0.07306', '-0.1626', '-0.2146', '0.317', '0.4983', '0.598', '-0.3682', '-0.7104', '-0.4412', '-0.615', '0.2935', '0.4976', '-0.0727', '0.3015', '0.11597', '-0.0783', '-0.8726', '-0.008675', '0.287', '0.2698', '-0.3196', '0.035', '-0.05063', '0.336', '-0.1365', '0.01419', '-0.818', '0.135', '-0.3337', '-0.2527', '-0.4863', '-0.4673', '0.1581', '-0.1571', '0.0837', '-0.2205', '0.3367', '0.4111', '-0.5063', '0.5503', '-0.2229', '-0.1001', '-0.01025', '-0.1469', '-0.535', '0.2676', '-0.1375', '-0.02783', '0.0706', '0.5605', '0.1836', '-0.1241', '0.1514', '-0.155', '-0.11755', '0.1095', '-0.04828', '-0.641', '0.02722', '-0.3503', '0.321', '0.0928', '-0.4705', '-0.2551', '0.4229', '-0.07336', '0.4663', '-0.5405', '-0.3914', '0.10675', '0.324', '0.1256', '0.1505', '-0.3733', '-0.298', '0.0944', '0.5005', '0.3105', '0.3796', '-0.535', '0.1725', '-0.0321', '-0.02048', '0.8916', '0.02078', '0.8564', '-0.476', '-0.09344', '-0.2505']",,,C535797,,,,
mondo:0008478,"spondylometaphyseal dysplasia, Schmidt type","['spondylometaphyseal dysplasia Algerian type', 'spondylometaphyseal dysplasia with severe genu valgum', 'Schmid metaphyseal dysostosis', 'spondylometaphyseal dysplasia, Schmidt type', 'spondylometaphyseal dysplasia Schmidt type', 'spondylometaphyseal dysplasia, Algerian type']",0112296,184253,93316,,,,,C535794,,,,
mondo:0008479,"spondylometaphyseal dysplasia, ^corner fracture^ type","['spondylometaphyseal dysplasia Sutcliffe type', 'spondylometaphyseal dysplasia corner fracture type', 'SMDCF', 'spondylometaphyseal dysplasia, corner fracture type', 'Sutcliffe SmD', 'spondylometaphyseal dysplasia, Sutcliffe type', 'Sutcliffe type of spondylometaphyseal dysplasia']",0112297,184255,93315,C0432221,"['-0.4094', '0.0951', '0.2573', '-0.03275', '0.3982', '-0.1757', '0.1049', '0.5986', '-0.265', '-0.2964', '-0.2915', '-0.0729', '-0.1951', '-0.1153', '-0.1731', '0.0716', '0.0286', '0.1236', '-0.2566', '-0.3137', '0.1592', '0.0365', '0.377', '-0.1674', '0.0831', '0.04797', '-0.2861', '-0.285', '0.2139', '0.001976', '0.2444', '-0.258', '0.328', '0.1862', '0.52', '-0.5347', '-0.1606', '-0.538', '0.08575', '-0.3718', '-0.08', '-0.3772', '-0.03983', '-0.10034', '0.02567', '-0.03165', '-0.1405', '0.52', '-0.2163', '-0.1395', '0.0809', '0.0555', '0.196', '0.1793', '-0.6787', '-0.625', '-0.1841', '-0.2236', '0.03732', '0.1648', '0.7085', '-0.1676', '-0.5015', '-0.286', '-0.1921', '-0.3643', '0.1575', '0.4136', '-0.606', '0.1941', '0.1067', '0.0406', '0.1526', '-0.2927', '-0.3188', '0.2098', '-0.4792', '0.08905', '-0.3252', '-0.379', '0.1597', '0.2642', '0.2087', '0.3245', '-0.1794', '0.05057', '-0.0821', '0.1747', '0.1487', '0.004852', '-0.1464', '0.04922', '-0.04443', '0.1445', '0.7573', '0.1289', '0.705', '-0.433', '0.1808', '0.1126']",,,C535793,,,,
mondo:0008481,"spondylosis, cervical","['spondylosis, cervical']",,184300,,C1384641,,,,,,,,
mondo:0008482,Sprengel deformity,"['Sprengel deformity (disease)', 'congenital elevation of the scapula', 'Sprengel^s deformity', 'high scapula', 'Sprengel deformity', 'Sprengel^s shoulder', 'congenital upward displacement of the scapula']",,184400,3181,,,,,C535802,,,10010455,0000912
mondo:0008483,"stuttering, familial persistent, 1","['STUT1', 'stuttering, familial persistent, 1', 'stammering']",,184450,,,,,,,,,,
mondo:0008484,stapes ankylosis with broad thumbs and toes,"['ankylosis of stapes, hyperopia, Broad thumbs, Broad first toes, and syndactyly', 'stapes ankylosis with BROAD thumb and toes', 'stapes ankylosis syndrome without symphalangism', 'Teunissen-Cremers syndrome']",,184460,140917,C1866656,"['-0.3044', '-0.001325', '0.3335', '0.1415', '0.391', '-0.3044', '0.04037', '0.5054', '-0.2634', '-0.3813', '-0.0758', '-0.2296', '-0.1808', '-0.1193', '0.02031', '0.1992', '0.605', '-0.2783', '-0.1343', '-0.4717', '0.0715', '0.198', '0.2142', '-0.2876', '0.5186', '0.2203', '-0.314', '0.109', '0.323', '-0.3381', '0.2676', '-0.4282', '-0.0645', '0.36', '0.1913', '-0.55', '-0.02386', '-0.27', '0.1516', '-0.1119', '-0.1566', '-0.3748', '0.0747', '-0.42', '0.1092', '-0.4377', '0.0944', '0.527', '-0.1831', '-0.1263', '-0.1047', '-0.2659', '-0.0446', '-0.08636', '-0.1777', '-0.602', '0.11884', '0.02003', '-0.0545', '0.2598', '0.1411', '-0.03503', '-0.0317', '-0.0521', '-0.2932', '0.003063', '-0.06323', '0.577', '-0.5195', '0.1797', '-0.3765', '0.1141', '0.1231', '-0.1364', '0.3855', '0.1271', '-0.0506', '-0.09827', '-0.2227', '-0.05417', '0.0665', '0.2646', '0.348', '0.846', '-0.067', '-0.11676', '-0.1332', '0.4712', '-0.1005', '0.2269', '-0.2324', '0.3572', '0.2617', '0.1426', '0.6685', '0.05878', '0.6016', '-0.929', '0.2366', '0.377']",,,,,,,
mondo:0008485,sebocystomatosis,"['multiple sebaceous cysts', 'sebaceous cysts, multiple', 'multiplex steatocystoma', 'Steatocystoma multiplex', 'STEATOCYSTOMA multiplex']",0111556,184500,841,C3671377,"['0.08777', '0.2108', '-0.5205', '0.1584', '0.1329', '-0.4612', '0.093', '0.4878', '-0.3142', '-0.2131', '-0.02438', '0.2091', '0.1344', '0.1625', '0.0516', '0.1316', '0.03488', '-0.1871', '0.09955', '-0.1636', '-0.3613', '0.03088', '0.5664', '-0.3027', '0.1864', '-0.04364', '-0.418', '-0.1399', '-0.1459', '0.05594', '0.617', '-0.324', '-0.0349', '-0.269', '0.1327', '0.0371', '-0.083', '-0.115', '0.01258', '0.1254', '0.0174', '-0.3406', '-0.1487', '-0.321', '0.2012', '0.2052', '-0.3188', '0.3027', '-0.4165', '-0.0699', '-0.2235', '-0.003765', '-0.02013', '-0.01907', '-0.1676', '0.0911', '0.6216', '-0.05774', '-0.2252', '0.04904', '0.2634', '0.0195', '0.0509', '0.05487', '-0.2328', '0.05017', '0.418', '0.6675', '-0.2183', '0.278', '0.3606', '0.02802', '0.2076', '0.06168', '0.2137', '0.2756', '0.05658', '0.2496', '-0.3008', '-0.1486', '-0.1351', '0.001379', '0.6226', '0.01907', '0.0665', '-0.05283', '-0.2222', '0.3235', '-0.01637', '-0.1935', '-0.03998', '0.1904', '0.1329', '0.02368', '0.6147', '-0.0531', '0.3423', '-0.657', '0.0427', '-0.2383']",,,,,,,
mondo:0008486,steatocystoma multiplex-natal teeth syndrome,"['Natal teeth and steatocystoma multiplex', 'STEATOCYSTOMA multiplex with NATAL teeth']",,184510,3184,C1866650,,,,C537487,,,,
mondo:0008487,polycystic ovary syndrome,"['Stein-Leventhal syndrome', 'PCO1', 'polycystic ovarian disease', 'Stein-Leventhal synd.', 'multicystic ovaries', 'PCOS1', 'PCOS', 'polycystic ovary', 'polycystic ovary syndrome 1', 'polycystic ovary syndrome', 'polycystic ovaries', 'hyperandrogenemia']",11612,184700,3185,C0032460,,C26862,0000660,D011085,256.4,,,
mondo:0008488,holoprosencephaly-radial heart renal anomalies syndrome,"['holoprosencephaly radial heart renal anomalies', 'STEINFELD syndrome', 'Steinfeld syndrome']",,184705,3186,C1866649,,,,C566655,,,,
mondo:0008489,"sternum, premature obliteration of sutures of","['sternum, premature obliteration of sutures of']",,184800,,,,,,,,,,
mondo:0008490,"otospondylomegaepiphyseal dysplasia, autosomal dominant","['Stickler syndrome, non-ocular type', 'heterozygous OSMED', 'Pierre Robin syndrome with fetal chondrodysplasia', 'Stickler syndrome nonocular type', 'Stickler syndrome, type III, formerly', 'Pierre Robin malformation', 'STL3', 'Piere-Robin syndrome', 'Pierre Robin syndrome with foetal chondrodysplasia Stickler syndrome, Nonocular type, formerly', 'Weissenbacher-Zweymuller syndrome', 'Weissenbacher-Zweymüller syndrome', 'heterozygous otospondylomegaepiphyseal dysplasia', 'OSMED, heterozygous', 'OSMEDA', 'STICKLER syndrome, type III', 'Stickler syndrome caused by mutation in COL11A2', 'Pierre Robin syndrome with foetal chondrodysplasia', 'Pierre Robin syndrome-fetal chondrodysplasia syndrome', 'otospondylomegaepiphyseal dysplasia, autosomal dominant', 'WZS', 'Stickler syndrome, Nonocular type', 'Stickler syndrome, type 3', 'Pierre Robin sequence-fetal chondrodysplasia syndrome', 'Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type', 'COL11A2 Stickler syndrome', 'Pierre Robin syndrome with foetal chondrodysplasia Stickler syndrome, Nonocular type', 'Weissenbacher- Zweymuller syndrome', 'Pierre Robin syndrome with fetal chondrodysplasia Stickler syndrome, Nonocular type, formerly']",4258,277610,3450,,"['0.625', '0.1305', '-0.3481', '0.2573', '0.385', '-0.7437', '0.02731', '1.12', '-1.154', '-0.6543', '0.5815', '-0.6353', '0.06647', '0.6133', '0.05667', '0.010605', '-0.3142', '0.5063', '-0.684', '-0.0722', '-0.1604', '0.316', '0.6', '0.288', '0.1064', '0.2935', '-1.023', '0.3794', '0.8394', '0.5713', '0.2275', '-0.06244', '-0.374', '0.2612', '-0.4275', '-0.04828', '-0.214', '-0.02151', '-0.1534', '-0.2137', '0.7515', '0.3503', '-0.5337', '-0.2722', '-0.3066', '-0.6064', '-0.0926', '0.1576', '0.2163', '-0.11664', '-0.4214', '0.4546', '0.7915', '-0.4172', '0.10956', '-0.4446', '-0.6006', '-0.0484', '-0.1482', '-0.2756', '0.9165', '0.04312', '-0.2695', '0.2059', '-0.4304', '0.1375', '0.667', '0.0947', '-0.3572', '0.5273', '0.365', '0.4475', '0.03003', '-0.5884', '-0.02776', '0.1622', '0.4658', '0.1868', '0.42', '0.6587', '0.10565', '-0.46', '0.01091', '1.024', '-0.594', '-0.05814', '0.1727', '0.6636', '0.0742', '0.3325', '-0.5664', '0.7334', '0.3013', '0.2883', '0.5186', '-0.01718', '0.7197', '-0.3267', '-0.2252', '0.22']",,,C537494,,,,
mondo:0008491,stiff-person syndrome,"['Morsch Woltman syndrome', 'SPS', 'stiff-person syndrome', 'Stiff man syndrome', 'stiff man syndrome', 'Stiff Person syndrome', 'SMS', 'Stiff-Man syndrome', 'Stiff-trunk syndrome', 'Moersch-Woltman syndrome', 'progressive encephalomyelitis with rigidity', 'Stiff-man syndrome', 'STIFF-PERSON syndrome', 'Stiff person syndrome and related disorders']",13366,184850,3198,C0085292,,C85170,0007498,D016750,333.91,,10042044,
mondo:0008492,stiff skin syndrome,"['stiff skin syndrome', 'STIFF skin syndrome', 'SSKS']",0111561,184900,2833,C1861456,"['-0.10876', '0.1432', '0.1254', '-0.001636', '0.4546', '-0.7207', '-0.1616', '0.2328', '-0.765', '-0.1367', '-0.398', '-0.06305', '-0.214', '0.4456', '0.1759', '0.4272', '0.01291', '-0.456', '-0.515', '-1.019', '0.3296', '-0.08307', '0.1823', '0.1266', '-0.0794', '-0.09906', '-0.2485', '-0.2167', '0.1251', '0.1317', '1.04', '-0.2203', '0.1095', '-0.2378', '0.08325', '-0.264', '-0.3804', '0.3357', '0.4788', '-0.0826', '0.1014', '-0.6816', '0.1505', '0.4448', '0.663', '0.01854', '-0.19', '-0.2233', '0.2012', '-0.672', '-0.114', '0.6167', '0.771', '0.5586', '0.02011', '-0.3645', '0.05466', '0.2275', '-0.0807', '-0.452', '0.1263', '0.1569', '-0.4075', '-0.2283', '-0.2773', '-0.0663', '-0.2212', '0.764', '0.0257', '0.3857', '-1.02', '0.2505', '0.095', '-0.001564', '0.192', '0.0732', '-0.2637', '-0.1257', '0.0817', '-0.662', '-0.08746', '0.1293', '0.1448', '0.302', '-0.4338', '0.697', '0.00679', '0.8057', '0.526', '0.0593', '-0.04727', '-0.003428', '0.1833', '0.1942', '0.10046', '-0.01232', '0.6924', '0.07855', '0.2144', '0.294']",C118636,,C566112,,,,
mondo:0008493,overhydrated hereditary stomatocytosis,"['Potassium sodium disorder of erythrocyte', 'OHS', 'OHST', 'stomatocytosis 1', 'overhydrated hereditary stomatocytosis', 'stomatocytosis I', 'Potassium-sodium disorder of erythrocyte', 'OVERHYDRATED hereditary stomatocytosis']",0111562,185000,3203,C1861455,"['-0.8145', '0.05615', '-0.3882', '0.3823', '-0.0894', '-0.02275', '-0.6885', '0.5645', '0.1489', '0.0264', '-0.504', '-0.1583', '0.0887', '-0.2069', '-0.258', '-0.08057', '-0.1289', '-0.0985', '-0.1483', '-1.026', '-0.3308', '0.05878', '0.6978', '0.2264', '-0.2656', '0.2421', '-0.1671', '0.4575', '0.1797', '-0.3237', '-0.2249', '-0.1716', '0.2966', '0.724', '-0.2817', '-0.9644', '-0.1937', '-0.3179', '0.2651', '-0.08777', '-0.3572', '0.174', '0.374', '0.01236', '0.10754', '-0.7734', '-0.8574', '-0.4666', '0.1318', '-0.1995', '0.2698', '-0.4941', '0.533', '1.087', '0.647', '-0.2622', '0.351', '0.3647', '-0.3213', '0.2347', '0.157', '0.1405', '0.6963', '-0.3594', '0.1287', '-0.1943', '0.418', '0.7397', '-0.5234', '0.765', '-0.1637', '-0.5454', '-0.2478', '0.6216', '0.5005', '0.1357', '0.209', '0.1863', '0.1191', '0.1094', '-0.0698', '-0.147', '-0.2205', '0.1389', '0.04047', '0.1556', '0.1088', '0.667', '0.405', '-0.6216', '1.195', '-0.0268', '0.1345', '-0.03873', '1.061', '0.725', '0.2517', '-0.6724', '0.382', '-0.5234']",,,C566111,,,,
mondo:0008494,cryohydrocytosis,"['hereditary cryohydrocytosis with normal stomatin', 'stomatocytosis, cold-sensitive', 'pseudohyperkalemia Cardiff', 'CHC', 'cryohydrocytosis']",,185020,398088,C1861453,"['-0.8477', '0.4397', '-0.02338', '0.1302', '0.1017', '-0.01755', '-0.588', '0.4238', '0.082', '-0.0375', '0.0764', '0.529', '0.0587', '-0.01778', '-0.1813', '-0.1954', '-0.1753', '0.056', '0.4172', '-0.5254', '-0.0194', '-0.1737', '0.5527', '0.4338', '0.2998', '0.09766', '-0.0968', '-0.0285', '-0.3699', '-0.02635', '-0.1263', '-0.04865', '0.317', '0.4888', '-0.3784', '-0.497', '-0.0474', '0.3704', '0.1111', '-0.3694', '-0.3867', '-0.297', '0.1349', '-0.1847', '-0.4104', '-0.3064', '-0.2028', '0.0695', '0.4746', '-0.4624', '-0.05103', '0.1886', '0.4917', '0.1506', '0.04434', '-0.12225', '0.208', '0.065', '-0.2878', '0.05554', '-0.1628', '-0.131', '0.2457', '-0.487', '0.1941', '-0.1509', '0.4778', '0.692', '-0.6426', '0.2426', '0.178', '-0.1337', '0.03354', '0.0996', '0.09503', '0.01284', '0.1515', '0.334', '-0.2412', '-0.1346', '-0.03415', '-0.5015', '-0.0542', '0.0512', '0.1127', '-0.541', '-0.1018', '0.187', '0.5957', '-0.1096', '0.5854', '0.2013', '0.2974', '-0.2057', '0.962', '0.717', '-0.05548', '-0.4785', '-0.2253', '0.2229']",,,C535827,,,,
mondo:0008495,platelet storage pool deficiency,"['dense body defect', 'storage pool platelet disease', 'alpha dense granule deficiency', 'platelet storage pool defect', 'combined alpha-delta platelet storage pool deficiency', 'platelet storage pool diseases', 'platelet dense granule deficiency', 'alpha delta granule deficiency']",2223,185050,734,,,,1001112,D010981,,,,
mondo:0008496,storm syndrome,"['storm syndrome', 'pleiotropic, autosomal dominant disorder affecting connective tissue']",,185069,,C1861452,,,,C566109,,,,
mondo:0008497,Stormorken syndrome,"['Stormorken syndrome', 'Thrombocytopathy, asplenia, and miosis', 'Thrombocytopathy-asplenia-miosis syndrome', 'york Platelet syndrome', 'Thrombocytopathy asplenia miosis', 'thrombocytopathy, asplenia and miosis', 'STRMK', 'Stormorken-Sjaastad-Langslet syndrome']",0060354,185070,3204,C1861451,"['-0.00419', '0.1542', '0.01788', '-0.04868', '0.08105', '-0.4387', '-0.093', '0.1881', '0.0707', '-0.2515', '-0.1511', '0.049', '-0.08075', '-0.0659', '0.08545', '0.132', '-0.06915', '-0.002375', '-0.1565', '-0.3875', '0.05542', '0.06064', '0.03067', '-0.2668', '-0.0538', '-0.1483', '-0.08936', '-0.1322', '0.04602', '-0.2131', '0.2136', '-0.2166', '0.07166', '-0.0397', '-0.06903', '-0.05804', '-0.2198', '-0.2122', '0.05026', '-0.1744', '0.1469', '-0.1967', '-0.02974', '-0.1721', '0.05847', '-0.2517', '-0.2332', '0.1483', '-0.2126', '-0.04837', '-0.07056', '-0.04514', '0.01338', '-0.06223', '0.3367', '-0.341', '0.3596', '0.05814', '-0.2988', '0.04736', '0.0791', '-0.1135', '0.0828', '-0.03555', '-0.1808', '-0.02754', '0.2092', '0.2076', '-0.37', '0.2644', '-0.295', '-0.05432', '-0.0999', '-0.1716', '0.1019', '0.281', '-0.11316', '0.1569', '-0.0009737', '-0.05124', '0.206', '0.324', '0.03015', '0.2605', '0.2957', '-0.02359', '0.1788', '0.3938', '0.10406', '0.2087', '0.0322', '0.2925', '0.06476', '0.1227', '0.611', '0.1786', '0.08124', '-0.347', '-0.149', '-0.0672']",,,C566108,759.89,,,
mondo:0008498,"strabismus, susceptibility to","['strabismus, susceptibility to', 'strabismus, susceptibility to, 1']",,185100,,C1861449,,,,,,,,
mondo:0008499,short stature-wormian bones-dextrocardia syndrome,"['Stratton-Parker syndrome', 'short stature wormian bones dextrocardia', 'STRATTON-PARKER syndrome', 'Growth hormone deficiency with Wormian bones, Cardiac anomaly, and Brachycamptodactyly', 'Stratton Parker syndrome']",,185120,2863,C1861448,,,,C566105,,,,
mondo:0008500,"striae distensae, familial","['striae distensae, familial']",,185200,,C1861447,,,,C566104,,,,
mondo:0008501,Sturge-Weber syndrome,"['Sturge-Weber syndrome', 'Sturge-Weber-Dimitri syndrome', 'Encephalofacial angiomatosis', 'Encephalotrigeminal angiomatosis', 'Sturge-Weber-Krabbe syndrome', 'Sturge Weber syndrome', 'leptomeningeal angiomatosis', 'fourth phacomatosis', 'Sturge-Weber disease', 'SWS type III - isolated leptomeningeal angiomas', 'Sturge-Weber syndrome, somatic, mosaic', 'Encephalotrigeminal syndrome', 'Sturge-Weber-Krabbe angiomatosis', 'SWS type I - Facial and leptomeningeal angiomas', 'SWS type II - Facial angioma alone, no CNS involvement', 'STURGE-WEBER syndrome', 'meningeal capillary angiomatosis', 'SWS']",0111563,185300,3205,CN204001,"['0.1721', '0.646', '-0.3203', '-0.4268', '0.02838', '0.03934', '0.8247', '0.3745', '-1.143', '-0.767', '-0.7695', '-0.2686', '1.093', '0.1218', '-0.3984', '-0.0643', '0.1483', '-0.2401', '-0.2133', '-0.479', '0.1396', '0.3325', '0.2229', '-0.0379', '-0.259', '-0.721', '0.1611', '0.00785', '0.275', '0.1324', '0.713', '0.1633', '-0.02261', '0.06616', '-0.348', '0.9014', '0.3257', '-0.07043', '-0.1721', '0.03084', '0.0967', '-0.2842', '0.5674', '-0.3389', '0.696', '0.01508', '0.01576', '0.09827', '0.12366', '0.4104', '-0.3237', '0.8716', '-0.3982', '-0.0401', '0.1896', '0.4395', '0.6157', '0.2079', '-0.5703', '0.2426', '-0.0438', '-0.1041', '0.1885', '0.0635', '-0.1439', '-0.03873', '0.565', '0.521', '-0.2935', '0.4731', '0.1755', '0.3306', '-0.3005', '0.2278', '0.3708', '0.12445', '0.6562', '-0.4663', '0.2034', '-0.4636', '-0.4148', '-0.03592', '-0.2129', '0.5317', '0.1816', '-0.061', '-0.328', '0.0973', '-0.01497', '-0.10297', '0.221', '0.02477', '-0.2795', '0.06604', '0.4312', '-0.4114', '0.7925', '-0.2642', '0.01061', '-0.0966']",C3391,,D013341,759.6,,10057653,
mondo:0008502,"sulfhemoglobinemia, congenital","['sulfhemoglobinemia, congenital']",,185460,,C1861437,,,,C566102,,,,
mondo:0008503,Worster-Drought syndrome,"['suprabulbar paresis, congenital', 'congenital suprabulbar paresis', 'suprabulbar paresis congenital', 'Worster Drought syndrome', 'Worster-Drought syndrome']",,185480,3465,C0796204,,,,C536747,,,,
mondo:0008504,supravalvular aortic stenosis,"['supravalvular aortic stenosis (disease)', 'supravalvar aortic stenosis', 'supravalvar aortic stenosis, Eisenberg type', 'supra-valvular aortic stenosis', 'SVAS', 'aortic supravalvular stenosis', 'supravalvular aortic stenosis']",1929,185500,3193,C0003499,"['-0.4265', '-0.0379', '-0.602', '0.1824', '0.2288', '-0.535', '0.56', '1.167', '-0.3318', '-0.3718', '-0.3882', '-0.2029', '0.2546', '0.4907', '-0.682', '-0.3203', '-0.588', '-0.53', '-0.4294', '-0.3943', '-0.08167', '0.09125', '0.9175', '-0.1975', '-0.1405', '0.0614', '0.7583', '0.8525', '0.7017', '0.3147', '0.522', '0.36', '0.4265', '0.1471', '-0.3198', '-0.01564', '0.04675', '0.0925', '0.4248', '-0.2314', '1.059', '0.04208', '0.799', '-0.04282', '-0.003328', '0.661', '-0.1935', '0.1768', '-0.10913', '-0.4487', '0.1299', '0.1361', '0.00894', '-0.08716', '0.09155', '-0.3528', '-0.07336', '0.05005', '-0.4834', '-0.2683', '-0.07794', '0.7505', '0.12427', '-0.3528', '0.007324', '0.3938', '0.6816', '-0.1143', '-0.51', '0.0886', '-0.2756', '0.2253', '0.126', '-0.1676', '-0.1881', '0.3093', '0.1719', '-0.2856', '-0.4138', '-0.4453', '-0.1608', '-0.4062', '0.1797', '0.2502', '0.1521', '0.1276', '0.5806', '0.321', '-0.1892', '-0.903', '0.1036', '-0.1127', '-0.2927', '0.2313', '1.03', '-0.2756', '0.539', '-0.082', '-0.709', '0.4885']",C85176,,,,,10042598,0004381
mondo:0008505,"surface antigen, glycoprotein 75","['surface glycoprotein 75', 'surface antigen, glycoprotein 75', 'surface antigen, glycoprotein type 75']",,185540,,,,,,,,,,
mondo:0008506,symphalangism of toes,['symphalangism of toes'],,185600,,C1861418,,,,C566101,,,,
mondo:0008507,"surface polypeptides, anonymous","['surface polypeptides, anonymous', 'Spa5', 'Spa2']",,185610,,,,,,,,,,
mondo:0008508,"symphalangism, C. S. Lewis type","['thumbs, stiff', 'symphalangism, C. S. Lewis type']",,185650,,C1861404,,,,C566100,,,,
mondo:0008509,distal symphalangism,"['Sym2', 'symphalangism, distal', 'distal symphalangism', 'distal symphalangism (disease)']",,185700,3248,C1861401,,,,C566099,,,,0100263
mondo:0008510,symphalangism with multiple anomalies of hands and feet,"['Learman syndrome', 'symphalangism with multiple anomalies of hands and feet']",,185750,3246,C1861391,,,,C566098,,,,
mondo:0008511,proximal symphalangism,"['vessel’s syndrome', 'hereditary absence of the proximal interphalangeal joints', 'hereditary absence of proximal interphalangeal joints', 'proximal symphalangism', 'Cushing^s symphalangism', 'Strasburger-Hawkins-Eldridge syndrome', 'Strasburger-Hawkins-Eldridge-Hargrave-McKusick syndrome', 'proximal symphalangism (disease)', 'symphalangism, Cushing type']",0050788,,3250,C1861385,"['-0.05203', '-0.1989', '0.2627', '-0.04376', '0.2522', '0.012474', '0.0989', '0.2438', '-0.2429', '0.0751', '0.03424', '-0.1986', '-0.15', '0.317', '0.00713', '-0.3633', '0.2861', '-0.3586', '0.10236', '-0.46', '-0.026', '0.238', '0.5146', '0.1254', '0.5474', '0.3347', '0.02243', '0.06915', '-0.0625', '0.194', '0.03256', '-0.4111', '0.0438', '0.3362', '0.08167', '-0.3445', '0.1404', '-0.1656', '-0.01682', '-0.532', '-0.07916', '-0.3484', '0.02998', '-0.12036', '0.2236', '-0.4597', '-0.05762', '0.4175', '0.1698', '0.1647', '-0.02254', '-0.335', '0.0772', '0.43', '-0.5596', '-0.2319', '0.0892', '0.0927', '-0.269', '-0.2947', '0.0491', '-0.1123', '-0.10455', '0.0723', '-0.3237', '0.0357', '0.1335', '0.4478', '-0.2336', '0.3342', '-0.231', '-0.1622', '0.2593', '-0.3408', '0.1826', '0.0264', '0.0383', '0.1556', '-0.1659', '-0.5874', '-0.1547', '0.2391', '0.493', '0.4336', '0.059', '-0.08093', '-0.5063', '0.243', '-0.04294', '0.01724', '-0.04462', '0.5874', '0.2495', '0.2179', '0.47', '-0.0325', '0.52', '-0.4766', '0.351', '0.2042']",,,C536223,,,,0100264
mondo:0008512,syndactyly type 1,"['Sd1', 'SDTY1', 'chromosome 2q35 DUPLICATION syndrome', 'syndactyly, type 1', 'Zygodactyly', 'craniosynostosis, Philadelphia type', 'syndactyly, type 1, with or without craniosynostosis']",0111816,185900,93402,C4275033,,,,,,,,
mondo:0008513,synpolydactyly type 1,"['SPD, Vordingborg type', 'synpolydactyly, Vordingborg type', 'synpolydactyly type 1', 'non-syndromic synpolydactyly caused by mutation in HOXD13', 'synpolydactyly 1', 'SD2a', 'SD2, Vordingborg type', 'HOXD13 non-syndromic synpolydactyly', 'syndactyly, type 2', 'SPD1', 'synpolydactyly with foot anomalies']",,186000,295195,CN203278,"['-0.3647', '-0.1057', '0.137', '0.06183', '0.1702', '-0.403', '-0.1449', '0.0793', '-0.4995', '-0.10626', '-0.08905', '-0.0706', '-0.1113', '-0.093', '-0.04886', '-0.1364', '0.1982', '-0.1888', '0.02245', '-0.294', '-0.00612', '0.1355', '0.3284', '-0.0789', '0.3018', '0.1932', '0.0993', '0.1447', '0.08887', '-0.2137', '0.0943', '-0.2507', '0.1708', '0.10486', '0.209', '-0.2094', '-0.00979', '-0.1449', '0.03635', '-0.3547', '-0.02899', '-0.2195', '0.08453', '0.039', '0.06155', '-0.3748', '0.1298', '0.2805', '0.106', '-0.2151', '-0.1819', '-0.128', '0.02847', '-0.0725', '-0.3735', '-0.41', '0.1682', '0.1646', '-0.3374', '0.01454', '0.0668', '0.03665', '-0.00822', '0.0554', '-0.0965', '0.2737', '0.1306', '0.05157', '-0.2184', '0.081', '-0.319', '0.09564', '0.0929', '-0.09644', '0.1283', '0.1901', '0.02052', '0.1521', '-0.2551', '-0.12445', '-0.1798', '-0.1089', '0.11273', '0.07434', '0.0689', '-0.267', '-0.00934', '0.4348', '0.08', '-0.01964', '-0.1765', '0.0646', '-0.006462', '-0.1227', '0.385', '0.05072', '0.4185', '-0.6064', '0.1337', '0.1456']",,,,,,,
mondo:0008514,syndactyly type 3,"['non-syndromic syndactyly caused by mutation in GJA1', 'Ring and Little finger syndactyly', 'GJA1 non-syndromic syndactyly', 'SD3', 'syndactyly of fingers 4 and 5', 'Sdty3', 'syndactyly, type 3', 'syndactyly of the ring and little finger', 'syndactyly of fingers four and five', 'syndactyly, type III']",0111817,186100,93404,C1861366,"['0.1602', '-0.02956', '0.3381', '0.2228', '0.516', '-0.2693', '-0.0858', '0.2993', '-0.3638', '-0.611', '-0.2607', '0.1061', '-0.27', '0.3455', '-0.1472', '-0.2537', '0.3054', '-0.3123', '0.05246', '-0.5435', '-0.26', '0.2225', '0.597', '-0.12', '0.4717', '0.143', '-0.1659', '0.11', '0.177', '0.0665', '-0.00447', '-0.627', '-0.1736', '0.0931', '0.1754', '-0.262', '0.12164', '-0.03375', '0.004097', '-0.559', '0.1565', '-0.2942', '0.2896', '0.014206', '0.5034', '-0.426', '-0.212', '0.4563', '0.0662', '0.00949', '0.349', '-0.11224', '0.173', '0.02463', '-0.4448', '-0.5366', '-0.03848', '-0.04745', '-0.32', '0.0709', '0.3687', '0.0685', '0.0522', '0.2856', '-0.2213', '0.1349', '0.2219', '0.2744', '-0.1048', '0.1495', '-0.1998', '0.0636', '0.3022', '-0.286', '0.2333', '0.1888', '-0.1498', '0.144', '-0.5747', '-0.919', '-0.4277', '-0.1879', '0.573', '0.43', '0.2451', '-0.2705', '-0.542', '0.2166', '-0.1295', '-0.4229', '0.04907', '0.524', '0.2043', '-0.02704', '0.5522', '-0.03763', '0.3816', '-1.21', '0.3118', '0.01974']",,,C538154,,,,
mondo:0008515,syndactyly type 4,"['non-syndromic syndactyly caused by mutation in LMBR1', 'SDTY4', 'Sd4', 'polysyndactyly type Haas', 'Haas type syndactyly', 'syndactyly, type IV', 'syndactyly, type 4', 'LMBR1 non-syndromic syndactyly', 'polysyndactyly, Haas type']",0111818,186200,93405,C1861355,"['0.02043', '-0.0832', '0.1335', '-0.0009193', '0.5703', '-0.1506', '-0.066', '0.3281', '-0.2578', '-0.4475', '-0.426', '0.1996', '-0.1514', '0.0342', '-0.198', '-0.10443', '0.523', '-0.1508', '-0.00876', '-0.608', '-0.08765', '0.3616', '0.58', '-0.2922', '0.282', '0.1576', '-0.1671', '-0.12195', '0.1506', '-0.109', '0.24', '-0.189', '0.01822', '-0.02905', '0.2085', '-0.391', '-0.1486', '-0.2278', '-0.2487', '-0.04657', '0.02182', '-0.3877', '0.1118', '-0.327', '0.1775', '-0.2502', '-0.4292', '0.509', '0.1459', '-0.1137', '0.03436', '-0.2345', '0.01293', '-0.208', '-0.561', '-0.3845', '0.05276', '-0.1691', '-0.2495', '-0.0654', '0.1731', '-0.004246', '0.2141', '0.1742', '-0.452', '0.0708', '0.1542', '0.3992', '0.01102', '0.0968', '-0.0912', '0.1786', '0.11945', '-0.3337', '0.2189', '-0.1128', '0.0513', '-0.124', '-0.438', '-0.599', '-0.2756', '0.2192', '0.6353', '0.369', '0.1736', '-0.1888', '-0.11334', '0.5186', '0.0898', '-0.1556', '0.0525', '0.4136', '0.1892', '-0.01541', '0.5405', '-0.03592', '0.4492', '-0.813', '0.1301', '0.3904']",,,C566092,,,,
mondo:0008516,syndactyly type 5,"['syndactyly with associated metacarpal and metatarsal fusion', 'SDTY5', 'SD5', 'postaxial syndactyly with metacarpal synostosis', 'syndactyly, type 5', 'syndactyly, type V', 'syndactyly with metacarpal and metatarsal fusion']",0111819,186300,93406,,"['-0.1344', '-0.010086', '0.2957', '0.11676', '0.319', '-0.504', '-0.0898', '0.3372', '-0.3413', '-0.727', '-0.3398', '0.1927', '-0.10254', '0.1731', '-0.2123', '-0.1956', '0.4163', '-0.2374', '0.003702', '-0.6113', '-0.2229', '0.293', '0.531', '-0.313', '0.399', '0.3528', '-0.1705', '0.1985', '0.1115', '-0.0818', '0.04517', '-0.7227', '-0.2067', '0.1011', '0.424', '-0.2727', '0.1039', '-0.112', '-0.02931', '-0.6626', '0.01077', '-0.492', '0.2722', '0.01008', '0.4856', '-0.4795', '-0.2426', '0.66', '0.03873', '-0.05884', '0.2261', '-0.01363', '0.1838', '0.03955', '-0.4731', '-0.595', '-0.01611', '-0.02882', '-0.1267', '0.03766', '0.287', '0.2285', '-0.2478', '0.3655', '-0.3167', '0.124', '0.1837', '0.3062', '-0.2998', '0.08014', '-0.3674', '0.01005', '0.3142', '-0.553', '0.374', '0.1599', '-0.3462', '-0.00812', '-0.529', '-0.6523', '-0.4463', '-0.1115', '0.599', '0.386', '0.323', '-0.247', '-0.7393', '0.3408', '-0.2512', '-0.7', '-0.06226', '0.3599', '0.1519', '-0.1324', '0.566', '0.06647', '0.5854', '-1.109', '0.548', '0.2169']",,,C538155,,,,
mondo:0008517,syndactyly-polydactyly-ear lobe syndrome,"['hallux syndactyly ulnar polydactyly abnormal ear lobes', 'syndactyly-polydactyly-earlobe syndrome', 'Spel syndrome']",,186350,3259,C1861347,,,,C566091,,,,
mondo:0008518,calcaneonavicular coalition,"['multiple synostosis syndrome', 'calcaneonavicular coalition', 'synostoses, tarsal, carpal, and digital', 'synostoses, tarsal, carpal and digital']",14762,186400,,C0175700,,,,C538156,755.8,,,
mondo:0008519,multiple synostoses syndrome 1,"['synostoses multiple with brachydactyly', 'symphalangism brachydactyly syndrome', 'Wl syndrome', 'facioaudiosymphalangism syndrome', 'nog multiple synostoses syndrome', 'NOG multiple synostoses syndrome', 'SYNS1', 'symphalangism-brachydactyly syndrome', 'multiple synostoses syndrome 1', 'multiple synostoses syndrome caused by mutation in nog', 'synostoses, multiple, with brachydactyly', 'multiple synostoses syndrome type 1', 'deafness-symphalangism syndrome of Herrmann']",0081317,186500,,C0342282,,,,,,,,
mondo:0008520,brachydactyly-elbow wrist dysplasia syndrome,"['brachydactyly-joint dysplasia syndrome', 'brachydactyly with joint dysplasia', 'brachydactyly with Joint dysplasia', 'synostosis, carpal, with dysplastic elbow joints and brachydactyly', 'LIEBENBERG syndrome', 'carpal synostosis with dysplastic elbow joints and brachydactyly', 'LBNBG', 'Liebenberg syndrome', 'brachydactyly elbow wrist dysplasia']",,186550,1275,C1861313,"['-0.0782', '0.1554', '0.08527', '0.014366', '0.1985', '-0.3943', '0.04745', '0.61', '-0.4324', '-0.3809', '-0.221', '0.1725', '-0.1227', '0.456', '0.393', '0.202', '0.1343', '0.26', '-0.4119', '-0.5776', '-0.2312', '0.321', '0.335', '-0.0628', '0.4846', '0.2012', '-0.3088', '0.473', '-0.02696', '0.2101', '0.1664', '-0.2573', '-0.3877', '0.492', '0.1667', '-0.2388', '0.2292', '-0.317', '0.3179', '-0.358', '-0.10236', '-0.3062', '-0.358', '0.0786', '0.2837', '-0.4624', '-0.1271', '0.3972', '0.681', '0.137', '0.06323', '-0.262', '0.06', '0.08984', '-0.1938', '-0.4314', '-0.03964', '-0.1073', '0.0901', '0.0223', '0.2964', '0.298', '-0.4634', '-0.09894', '-0.4055', '-0.14', '0.0653', '0.686', '-0.1558', '-0.0006924', '-0.545', '0.2156', '0.0327', '-0.216', '0.1038', '0.1775', '-0.4695', '0.4275', '-0.3596', '-0.641', '-0.0341', '-0.001149', '0.4604', '0.2134', '-0.155', '0.2227', '-0.0822', '0.598', '0.09955', '-0.0375', '-0.2798', '0.3005', '-0.2142', '0.2247', '0.2517', '0.10846', '0.5957', '-0.7446', '0.1927', '0.3306']",,,C566090,,,,
mondo:0008521,tarsal-carpal coalition syndrome,"['tarsal carpal coalition syndrome', 'TCC', 'tarsal-carpal coalition syndrome', 'synostosis of talus and calcaneus with short stature']",0050789,186570,1412,C1861305,"['-0.1973', '0.1228', '0.001416', '0.04156', '0.1378', '-0.626', '-0.0409', '0.559', '-0.3894', '-0.4453', '-0.1995', '0.127', '-0.04697', '0.1093', '0.1142', '0.0994', '0.4224', '-0.1866', '-0.01587', '-0.4392', '-0.157', '0.1624', '0.2625', '-0.3125', '0.523', '0.4546', '0.0756', '0.06033', '0.0234', '0.1467', '0.09174', '-0.4614', '-0.0343', '0.3086', '0.3823', '-0.2952', '0.1063', '-0.3025', '-0.03134', '0.05325', '-0.2305', '-0.4287', '0.11584', '0.01692', '0.0971', '0.044', '-0.1599', '0.2377', '-0.2656', '-0.2969', '0.0273', '-0.04276', '-0.05814', '0.169', '-0.283', '-0.3887', '0.1294', '-0.1092', '-0.02423', '-0.0893', '0.5684', '0.1564', '-0.24', '0.1127', '-0.1943', '-0.3174', '0.27', '0.4155', '-0.1487', '-0.0663', '-0.3445', '0.1792', '0.2979', '-0.295', '0.0742', '0.2378', '-0.2532', '0.10974', '-0.266', '-0.2144', '0.18', '0.2915', '0.2185', '0.544', '0.08826', '0.0922', '-0.2424', '0.401', '0.04388', '-0.2466', '0.02776', '0.1559', '0.066', '0.124', '0.6543', '0.0773', '0.5527', '-0.7295', '0.4087', '0.2495']",,0008965,,756.9,,,
mondo:0008522,"synovial chondromatosis, familial, with dwarfism","['synovial chondromatosis, familial, with dwarfism', 'synovial chondromatosis, familial with dwarfism']",,186575,,C1861304,,,,C566087,,,,
mondo:0008523,Blau syndrome,"['BLAUS', 'granulomatosis, familial juvenile systemic', 'granulomatous inflammatory arthritis, dermatitis, and uveitis, familial', 'EOS', 'Jabs syndrome', 'arthrocutaneouveal granulomatosis', 'sarcoidosis, early-onset', 'synovitis granulomatous with uveitis and cranial neuropathies', 'synovitis, granulomatous, with uveitis and cranial neuropathies', 'ACUG', 'pediatric granulomatous arthritis', 'paediatric granulomatous arthritis', 'early-onset sarcoidosis', 'Blau syndrome', 'granulomatosis, familial, Blau type']",0050678,609464,90341,C1861303,"['0.354', '0.2472', '-0.3943', '0.2837', '0.02556', '-0.3792', '0.2786', '0.2576', '-0.5435', '0.2225', '-0.4543', '0.2185', '0.369', '0.00673', '-0.04132', '-0.02951', '0.3215', '-0.02141', '0.59', '-1.076', '-0.1807', '-0.292', '0.6562', '-0.2377', '-0.1438', '0.4817', '-0.3816', '0.9316', '-0.1743', '0.6255', '0.6865', '-0.3342', '0.2566', '-0.005264', '-0.2354', '-0.00593', '-0.1234', '-0.853', '0.10156', '-0.2064', '-0.3235', '-0.627', '0.2761', '0.09845', '1.086', '0.8276', '-0.4055', '0.2499', '0.5103', '0.3806', '-0.3164', '0.4053', '0.2566', '0.09076', '0.1936', '-0.371', '0.7163', '-0.2583', '-0.5903', '-0.2012', '-0.2308', '-0.10065', '-0.4683', '-0.279', '0.3157', '-0.161', '0.565', '0.314', '0.0461', '0.2856', '0.2035', '-0.3813', '0.1047', '-0.00651', '0.2292', '0.1604', '-0.00885', '0.1732', '0.1788', '-0.03128', '-0.2319', '0.1182', '-0.2441', '0.0381', '-0.0963', '0.01234', '0.283', '0.6304', '0.1716', '0.557', '0.6006', '0.05887', '-0.0853', '-0.4062', '0.757', '-0.1753', '0.1996', '-0.3015', '-0.04453', '-0.5337']",C116794,,C538157,714.89,,10071755,
mondo:0008524,"syringomas, multiple","['syringomas, multiple']",,186600,,C1861302,,,,C566085,,,,
mondo:0008525,"syringomyelia, isolated","['syringomyelia, noncommunicating isolated', 'syringomyelia, isolated']",,186700,,,,,,C566084,,,,
mondo:0008526,talonavicular coalition,['talonavicular coalition'],,186750,,,,,,C536895,,,,
mondo:0008527,tarsal coalition,"['tarsal coalition', 'tarsal fusion']",,186850,,,,,,D000070604,755.67,,,
mondo:0008528,"tear protein, anodal","['tear protein, anodal']",,186890,,C1861283,,,,,,,,
mondo:0008529,"T-cell Subgroups, non-HLA-linked","['T-cell Subgroups, non-HLA-linked']",,186950,,,,,,,,,,
mondo:0008530,"teeth, odd shapes of","['Lobodontia', 'teeth, odd shapes of', 'conical teeth, multiple']",,187000,,C1861274,,,,C566076,,,,
mondo:0008532,teeth present at birth,"['teeth present at birth', 'teeth present at birth (disease)', 'teeth present AT birth', 'Natal teeth']",,187050,,,,,,,,,,0000695
mondo:0008533,"teeth, supernumerary","['teeth, supernumerary']",,187100,,,,,,D014096,,K00.1,,
mondo:0008534,generalized essential telangiectasia,"['telangiectasia, hereditary benign', 'Hbt', 'telangiectasia, generalised essential', 'telangiectasia, generalized essential', 'GET']",,187260,280774,C0473555,,,,,,,,
mondo:0008535,"telangiectasia, hereditary hemorrhagic, type 1","['ORW disease', 'telangiectasia, hereditary hemorrhagic, type 1', 'hereditary hemorrhagic telangiectasia type 1', 'ENG-related Hereditary hemorrhagic telangiectasia', 'HHT', 'Osler Weber Rendu syndrome type 1', 'telangiectasia, hereditary hemorrhagic, of Rendu, Osler, and Weber', 'Osler-Rendu-Weber disease', 'telangiectasia, hereditary hemorrhagic, of RENDU, Osler, and WEBER', 'HHT1']",,187300,,CN034812,,,,,,,,
mondo:0008536,temperature-sensitive lethal mutation,['temperature-sensitive lethal mutation'],,187340,,,,,,,,,,
mondo:0008537,telecanthus,['telecanthus'],,187350,98575,,,,,C562941,,,,
mondo:0008538,temporal arteritis,"['Horton’s disease', 'polymyalgia rheumatica', 'Horton^s arteritis', 'Horton^s giant cell arteritis', 'cranial arteritis', 'arteritis cranialis', 'giant cell arteritis', 'Horton^s disease', 'temporal artery inflammation', 'Horton disease', 'temporal arteritis', 'GCA', 'arteritis temporalis', 'Horton’s syndrome', 'Horton^s temporal arteritis']",13375,187360,397,C1956391,,C35065,1001209,,446.5,,10043207,
mondo:0008540,extensor tendons of finger anomalies,"['anomalous insertion of extensor tendons of fingers', 'tendons, extensor, of fingers, anomalous insertion OF', 'Hapnes Boman Skeie syndrome', 'Hapnes-Boman-Skeie syndrome']",,187390,3294,C2931376,,,,C566068,,,,
mondo:0008541,spermatic cord torsion,"['torsion of testicular cord', 'torsion of testicle', 'torsion of testis', 'testicular torsion']",11996,187400,,C0037856,,C26885,,D013086,608.20,,,
mondo:0008542,tetralogy of fallot,"['TOF', 'Fallot tetralogy', 'tetralogy of fallot', 'ventricular septal defect with pulmonary stenosis or atresia, dextraposition of aorta, and hypertrophy of right ventricle', 'tetralogy of FALLOT']",6419,187500,3303,C0039685,,C84505,,D013771,745.2,Q21.3,10016193,
mondo:0008543,tetralogy of fallot and glaucoma,"['familial tetralogy of fallot and glaucoma', 'tetralogy of fallot and glaucoma']",,187501,,C1861234,,,,C536501,,,,
mondo:0008544,tetramelic monodactyly,"['Sommer Hines syndrome', 'Sommer-Hines syndrome', 'tetramelic monodactyly with autosomal dominant inheritance', 'tetramelic monodactyly']",,187510,2564,C1861233,,,,C566066,,,,
mondo:0008545,"thalassemia, beta+, silent allele","['thalassemia, beta+, silent allele']",,187550,,C1861232,,,,C566065,,,,
mondo:0008546,thanatophoric dysplasia type 1,"['thanatophoric dysplasia, type I', 'TD1', 'Platyspondylic lethal skeletal dysplasia, San Diego type', 'lethal short-limbed Platyspondylic dwarfism, San Diego type', 'thanatophoric dwarfism type 1', 'type 1 thanatophoric dysplasia', 'thanatophoric dwarfism', 'thanatophoric dwarfism 1', 'thanatophoric dysplasia type I', 'PLSD San Diego type', 'thanatophoric dysplasia, type 1', 'thanatophoric dysplasia']",,270230,1860,C1868678,"['-0.11224', '0.3438', '0.06635', '-0.2722', '0.2383', '-0.4111', '0.1771', '0.851', '-0.694', '-0.5244', '-0.2311', '0.10516', '0.002806', '-0.00968', '-0.4187', '-0.1932', '0.2251', '-0.1428', '0.2103', '-0.884', '-0.0732', '-0.06235', '0.9243', '-0.1318', '-0.1305', '0.05203', '-0.2369', '-0.06555', '0.3384', '-0.1556', '-0.02272', '0.1948', '-0.05695', '-0.02214', '0.02963', '-0.005165', '-0.4053', '-0.222', '0.0506', '0.0249', '-0.07556', '-0.3765', '0.0846', '0.1804', '-0.2246', '0.3276', '-0.05582', '0.6763', '0.3376', '-0.1953', '0.72', '-0.57', '-0.4094', '-0.0853', '-0.2832', '-0.7095', '-0.3225', '-0.571', '0.5933', '0.7163', '-0.0509', '0.4443', '-0.329', '-0.1558', '0.01059', '-0.1964', '0.379', '0.04578', '-0.545', '0.5015', '0.302', '0.1497', '0.8237', '-0.1737', '-0.3923', '0.4375', '-0.2494', '0.2393', '-0.663', '-0.4917', '-0.011566', '0.3652', '-0.1704', '-0.066', '-0.37', '0.494', '0.3018', '0.1276', '0.9883', '-0.2423', '0.1602', '0.2252', '0.3083', '-0.03156', '0.765', '0.1488', '0.6084', '-0.4905', '0.2893', '0.1567']",C98583,,,,,,
mondo:0008547,thanatophoric dysplasia type 2,"['type 2 thanatophoric dysplasia', 'thanatophoric dysplasia with Kleeblattschaedel', 'thanatophoric dysplasia type II', 'cloverleaf skull-micromelic bone dysplasia syndrome', 'cloverleaf skull with thanatophoric dwarfism', 'thanatophoric dwarfism type 2', 'thanatophoric dysplasia with straight femurs and cloverleaf skull', 'thanatophoric dysplasia, type 2', 'thanatophoric dysplasia, type II', 'TD2', 'thanatophoric dwarfism - cloverleaf skull', 'thanatophoric dwarfism-cloverleaf skull syndrome']",,187601,93274,CN206542,"['-0.235', '0.1718', '0.3035', '-0.4434', '0.1852', '-0.5522', '0.05933', '0.6123', '-0.885', '-0.6045', '0.03111', '0.0853', '-0.02122', '-0.0674', '-0.2578', '-0.2607', '0.1748', '-0.5854', '0.1161', '-0.689', '-0.01401', '0.0447', '0.823', '-0.082', '-0.0319', '0.009155', '-0.305', '-0.1278', '0.396', '-0.2727', '-0.0876', '0.1555', '-0.0741', '0.1509', '-0.0457', '-0.00517', '-0.05164', '-0.2932', '0.1467', '-0.2607', '-0.02739', '-0.2368', '0.2389', '0.2142', '-0.2593', '0.0926', '0.014244', '0.591', '0.3936', '-0.1664', '0.8286', '-0.4917', '-0.2311', '-0.2898', '-0.273', '-0.63', '-0.09784', '0.01062', '0.5415', '0.487', '0.028', '0.3303', '-0.4707', '-0.3171', '0.0398', '-0.364', '0.285', '0.3457', '-0.6406', '0.4019', '0.1072', '0.1272', '0.725', '-0.11163', '-0.4526', '0.683', '-0.0564', '0.1587', '-0.8174', '-0.463', '-0.2277', '0.133', '-0.1125', '0.2238', '-0.4187', '0.4958', '0.3733', '0.0357', '0.958', '-0.1189', '-0.4358', '0.2976', '0.4563', '0.0783', '0.351', '0.425', '0.744', '-0.3525', '0.361', '0.0818']",C98584,,C536508,742.59,,,
mondo:0008549,"thoracic dysostosis, isolated","['thoracic dysostosis, isolated']",,187750,,C1861204,,,,C566063,,,,
mondo:0008551,thoracolaryngopelvic dysplasia,"['thoracopelvic dysostosis', 'TLPD', 'autosomal dominant thoracolaryngopelvic dysplasia', 'Barnes syndrome', 'thoracolaryngopelvic dysplasia']",,187770,3317,C1861197,,,,C536517,,,,
mondo:0008552,platelet-type bleeding disorder 16,"['autosomal dominant thrombasthenia of Glanzmann and Naegeli', 'BDPLT16', 'thrombasthenia of Glanzmann and Naegeli, autosomal dominant', 'bleeding disorder, platelet-type, 16, autosomal dominant', 'Glanzmann thrombasthenia, autosomal dominant', 'bleeding disorder, platelet-type, 16', 'autosomal dominant Glanzmann thrombasthenia']",0060691,187800,140957,C1861195,"['-0.2546', '0.2961', '-0.1414', '-0.383', '0.352', '-0.3147', '-0.1091', '0.3423', '0.2255', '-0.8145', '-0.01423', '-0.0459', '-0.05408', '-0.518', '-0.04153', '0.1986', '-0.03915', '0.11383', '0.0672', '-0.4983', '-0.138', '-0.09686', '0.3457', '-0.319', '0.3955', '0.2325', '-0.384', '-0.08026', '0.4407', '-0.0895', '0.1427', '-0.02698', '0.2715', '0.2332', '-0.2834', '-0.8774', '-0.2954', '-0.1411', '-0.3127', '-0.2578', '0.1405', '-0.1398', '-0.127', '-0.0318', '-0.3955', '-0.707', '-0.1692', '0.1385', '0.5356', '-0.549', '0.1754', '-0.465', '0.3035', '0.02855', '-0.216', '-0.1995', '0.7437', '-0.02325', '-0.4917', '0.2472', '0.1808', '0.09326', '0.10504', '-0.1759', '-0.2256', '-0.7075', '-0.0556', '0.2478', '-0.606', '0.2937', '0.003738', '0.0393', '-0.09094', '0.02116', '0.6914', '0.6445', '0.0848', '0.2725', '-0.2297', '0.08673', '0.00473', '0.06216', '0.345', '-0.12067', '-0.319', '0.11566', '0.4424', '0.9214', '-0.1328', '0.03017', '-0.1665', '0.3464', '-0.05295', '-0.1583', '0.5947', '0.6763', '0.5176', '-0.558', '-0.1455', '0.2393']",,,C566061,,,,
mondo:0008553,platelet-type bleeding disorder 17,"['bleeding disorder, platelet-type, 17', 'GFI1B inherited bleeding disorder, platelet-type', 'thrombasthenia-thrombocytopenia, hereditary', 'hereditary thrombasthenia-thrombocytopenia', 'bleeding disorder, platelet-type 17', 'inherited bleeding disorder, platelet-type caused by mutation in GFI1B', 'BDPLT17']",0111049,187900,,,,C142084,,C566060,,,,
mondo:0008554,thrombocythemia 1,"['thrombocythemia, somatic', 'thrombocytosis 1', 'THCYT1', 'thrombocythemia type 1', 'thrombocythemia 1']",,187950,71493,C3277671,,,,,,,,
mondo:0008555,thrombocytopenia 2,"['thrombocytopenia autosomal dominant 2', 'thrombocytopenia, autosomal dominant, 2', 'THC2', 'thrombocytopenia 2', 'thrombocytopenia type 2']",,188000,,,,C129035,,C536519,,,,
mondo:0008556,"thrombocytopenia, cyclic","['cyclic thrombocytopenia', 'thrombocytopenia, cyclic', 'thrombocytopenia cyclic']",,188020,,C0272282,,,,C536899,287.39,,,
mondo:0008557,Paris-Trousseau thrombocytopenia,"['thrombocytopenia Paris-Trousseau type', 'Paris-Trousseau syndrome', 'chromosome 11q23 deletion syndrome', 'TCPT', 'thrombocytopenia, Paris-Trousseau type, Isolated cases', 'thrombocytopenia, Paris-TROUSSEAU type']",,188025,851,C1956093,,,,,,,,
mondo:0008558,autoimmune thrombocytopenic purpura,"['ITP', 'idiopathic purpura', 'ideopath thrombocytopenic pur', 'immune thrombocytopenic purpura', 'idiopathic thrombocytopenia', 'thrombocytopenic purpura autoimmune', 'AITP', 'thrombocytopenic purpura, autoimmune', 'immune thrombocytopenia', 'primary thrombocytopenic purpura', 'idiopathic thrombocytopenia purpura', 'Werlhof^s disease', 'idiopathic thrombocytopenic purpura', 'autoimmune thrombocytopenic purpura']",8924,188030,3002,,,C3446,0007160,,287.31,,10021245,
mondo:0008559,thrombophilia due to thrombin defect,"['thromboembolism, susceptibility to', 'THPH1', 'thrombophilia due to thrombin defect', 'hyperprothrombinemia', 'venous thrombosis, protection against', 'thrombophilia due to factor 2 defect', 'factor II-related thrombophilia', 'thrombosis, protection against', 'venous thrombosis', 'prothrombin-related thrombophilia', 'prothrombin thrombophilia', 'prothrombin 20210G>A thrombophilia', 'prothrombin G20210A thrombophilia', 'Venous thromboembolism', 'thrombophilia 1 due to thrombin defect', 'venous thromboembolism, susceptibility to']",0111907,188050,,,,,,,453.9,,,
mondo:0008560,thrombophilia due to activated protein C resistance,"['Activated Protein C resistance', 'thrombophilia 5', 'Pccf deficiency', 'thrombophilia 2 due to activated protein C resistance', 'THPH2', 'thrombophilia due to Factor 5 Leiden', 'APC resistance', 'thrombophilia due to ACTIVATED PROTEIN C resistance', 'thrombophilia due to activated protein C resistance', 'thrombophilia, susceptibility to, due to factor V Leiden', 'resistance, APC', 'thrombophilia due to deficiency of Activated Protein C cofactor', 'Proc cofactor deficiency']",0111902,188055,,C1861171,,,,D020016,289.81,,,
mondo:0008561,thumb deformity,"['thumb hypoplastic', 'thumb absent or hypoplastic', 'thumb deformity', 'thumb deformity (disease)']",,188100,,,,,,C536903,,,,0001172
mondo:0008562,thumb deformity-alopecia-pigmentation anomaly syndrome,"['congenital deformity of the thumb and congenital alopecia', 'hypotrichosis associated with congenital hypoplasia of the thumb', 'thumb deformity and alopecia', 'thumb deformity, alopecia, pigmentation anomaly', 'sparse hair, short stature, hypoplastic thumbs, single upper central incisor and abnormal skin pigmentation']",,188150,2251,C2931366,,,,C566054,,,,
mondo:0008563,thumb stiffness-brachydactyly-intellectual disability syndrome,"['thumbs, STIFF, with brachydactyly type A1 and developmental delay', 'Thumb ankylosis with intellectual disability', 'thumb stiff brachydactyly mental retardation', 'Thumb ankylosis with mental retardation', 'thumb stiff brachydactyly intellectual disability', 'Piussan-Lenaerts-Mathieu syndrome']",,188201,1078,,,,,,,,,
mondo:0008564,DiGeorge syndrome,"['Shprintzen syndrome', 'DGS1', 'Catch22', 'hypoplasia of thymus and parathyroids', 'Takao VCF syndrome', '22q deletion syndrome(s)', 'DiGeorge syndrome', '22q11.2 Deletion syndrome', 'velocardiofacial syndrome', 'DGS', 'DiGeorge syndrome chromosome region', 'DiGeorge^s syndrome', 'Sphrintzen', 'VCF', 'third and fourth pharyngeal pouch syndrome', 'DiGeorge anomaly', 'chromosome 22Q11.2 deletion syndrome', 'pharyngeal pouch syndrome', 'Di-George syndrome', 'DiGeorge syndrome type 1', 'velo-cardio-facial syndrome']",11198,188400,,CN734570,,C2989,,D004062,279.11,,,
mondo:0008565,familial thyroglossal duct cyst,"['thyroglossal duct cysts', 'thyroglossal duct cysts familial', 'thyroglossal duct cyst, familial', 'hereditary thyroglossal duct cysts', 'hereditary thyroglossal duct cyst']",,188455,93953,C3495590,,,,C536909,,,,
mondo:0008566,"thyroid cancer, nonmedullary, 2","['thyroid cancer, nonmedullary, type 2', 'thyroid cancer, nonmedullary, 2, autosomal dominant, somatic mutation', 'thyroid cancer, nonmedullary, 2', 'FTC', 'thyroid carcinoma, follicular, autosomal dominant, somatic mutation', 'thyroid carcinoma, follicular', 'thyroid cancer, follicular', 'NMTC2', 'thyroid carcinoma, follicular, somatic']",,188470,,,,,,C572845,,,,
mondo:0008567,"thyroid cancer, nonmedullary, 1","['thyroid cancer, nonmedullary, 1', 'nonmedullary thyroid carcinoma, papillary', 'thyroid cancer, nonmedullary, type 1', 'papillary carcinoma of thyroid', 'familial nonmedullary thyroid cancer, papillary', 'NMTC1']",,188550,319487,,,,,,,,,
mondo:0008568,thyroid hormone plasma membrane transport defect,"['hyperthyroxinemia, Eumetabolic, due to T4 plasma Membrane Transport', 'defect', 'thyroid hormone resistance due to T4 plasma Membrane Transport defect', 'thyroid hormone plasma membrane transport defect']",,188560,,C1861101,,,,C536916,,,,
mondo:0008569,"thyroid hormone resistance, generalized, autosomal dominant","['GRTH', 'thyroid hormone resistance', 'hyperthyroxinemia, familial euthyroid, secondary to pituitary and peripheral resistance to thyroid hormones', 'thyroid hormone resistance, generalized, autosomal dominant', 'Gthr', 'thyroid hormone unresponsiveness']",,188570,,C2937288,,,,C567934,,,,
mondo:0008570,"thyrotoxic periodic paralysis, susceptibility to, 1","['thyrotoxic periodic paralysis, susceptibility to, 1', 'TTPP1', 'thyrotoxic periodic paralysis, susceptibility to, type 1', 'thyrotoxic periodic paralysis caused by mutation in CACNA1S', 'CACNA1S thyrotoxic periodic paralysis']",,188580,,,,,,,,,,
mondo:0008571,"Blount disease, infantile","['Osteochondrosis deformans tibiae, infantile', 'tibia vara, infantile', 'Blount disease, infantile']",,188700,,C3150037,,,,,,,,
mondo:0008572,"tibia, hypoplasia or aplasia of, with polydactyly","['polydactyly with absent tibia', 'THYP', 'hypoplastic or aplastic tibia with polydactyly', 'absence of tibia with polydactyly', 'tibia, hypoplasia or aplasia of, with polydactyly', 'Werner mesomelic syndrome', 'hypoplastic tibiae-postaxial polydactyly syndrome', 'tibial hemimelia-polysyndactyly-triphalangeal thumb syndrome', 'absent tibia-polydactyly syndrome', 'tibial hemimelia-polydactyly-triphalangeal thumbs with fibular dimelia']",0111564,188740,988,CN204341,"['-0.06113', '0.05786', '0.04944', '-0.06122', '0.06464', '-0.08386', '-0.007633', '0.1157', '-0.1063', '-0.106', '-0.05814', '-0.04108', '-0.03928', '0.02995', '-0.06976', '-0.0296', '0.0373', '-0.084', '-0.03177', '-0.1779', '-0.02257', '-0.03079', '0.1445', '-0.03406', '0.0822', '-0.002203', '-0.02797', '0.004177', '0.0389', '-0.08826', '0.0806', '-0.04642', '0.07574', '0.03757', '0.10706', '-0.0778', '-0.002087', '-0.02643', '-0.0159', '-0.0903', '0.02379', '-0.05835', '-0.001028', '-0.05753', '0.0081', '-0.0956', '-0.0002947', '0.1216', '0.01391', '0.013214', '-0.0314', '-0.0447', '-0.000492', '-0.0037', '-0.099', '-0.081', '0.0322', '-0.06274', '-0.10144', '0.01498', '0.06006', '0.03976', '-0.0515', '0.03995', '-0.04605', '-0.02995', '0.0687', '0.08124', '-0.0869', '0.08997', '-0.05435', '0.05823', '0.0753', '-0.04678', '0.0645', '0.0323', '0.01796', '-0.06076', '-0.09424', '-0.10535', '-0.0814', '-0.02278', '0.02617', '0.1107', '-0.02638', '-0.00886', '-0.03436', '0.1151', '0.07043', '-0.04437', '-0.02367', '0.0925', '0.02948', '0.01561', '0.2203', '-0.051', '0.12', '-0.1511', '0.03763', '0.04138']",,,C566046,,,,
mondo:0008573,"tibial torsion, bilateral medial","['tibial torsion, bilateral medial']",,188800,,C1861097,,,,C566045,,,,
mondo:0008575,nicotine dependence,"['nicotine addiction', 'tobacco use disorder']",0050742,,,,,C54203,0003768,D014029,305.1,F17,,
mondo:0008576,"toe, fifth, number of phalanges 1N","['toe, fifth, number of phalanges type 1N', 'toe, fifth, number of phalanges IN']",,189000,,,,,,,,,,
mondo:0008577,"toe, misshapen","['toe, misshapen']",,189100,,,,,,,,,,
mondo:0008578,"toe, rotated fifth","['toe, rotated fifth']",,189150,,,,,,,,,,
mondo:0008579,"toes, relative length of first and second","['toes, relative length of first and second']",,189200,,,,,,,,,,
mondo:0008580,"toes, space between first and second","['toes, space between first and second']",,189230,,,,,,,,,,
mondo:0008581,malposition of teeth with or without hypodontia/oligodontia,"['ectopic eruption of teeth', 'malposition of teeth with or without hypodontia/oligodontia']",,189490,,,,,,,,,,
mondo:0008582,tooth and nail syndrome,"['hypoplastic enamel-onycholysis-hypohidrosis syndrome', 'WITKOP syndrome', 'hypodontia and nail dysplasia', 'HND', 'tooth and nail syndrome', 'tooth-and-nail syndrome', 'dysplasia of nails with hypodontia', 'hypodontia-nail dysgenesis syndrome', 'hypodontia with nail dysplasia', 'hypodontia-nail dysplasia', 'Witkop^s syndrome', 'nail dysplasia with hypodontia', 'Witkop syndrome', 'TNS', 'hypodontia - dysplasia of nails', 'ectodermal dysplasia 3, Witkop type', 'ectodermal dysplasia 3, Tooth/nail type', 'hypodontia-dysplasia of nails syndrome']",6678,189500,2228,C0406735,"['0.0802', '0.11237', '-0.1798', '-0.2255', '0.5293', '-0.238', '-0.19', '0.6284', '-0.253', '-0.3638', '-0.392', '-0.4307', '-0.3726', '-0.251', '0.2211', '0.4006', '0.1825', '-0.28', '-0.6523', '-0.5664', '-0.527', '-0.3276', '0.64', '-0.2954', '0.701', '-0.03986', '-0.4995', '0.2424', '-0.0491', '-0.4556', '0.728', '-0.1431', '-0.5884', '0.05225', '0.182', '0.427', '-0.09204', '-0.2869', '0.0757', '-0.2175', '-0.0672', '-0.05573', '-0.15', '-0.538', '-0.2063', '-0.208', '0.0671', '-0.2537', '0.275', '-0.6255', '0.05847', '-0.1454', '0.044', '0.3108', '-0.5063', '-0.2625', '0.4084', '-0.5293', '-0.0794', '-0.4248', '0.1182', '0.1843', '-0.1493', '-0.254', '0.01078', '0.2249', '0.3123', '0.5605', '0.0649', '0.9634', '-0.4705', '-0.287', '-0.04147', '0.2603', '0.1766', '0.2517', '-0.2147', '-0.1794', '0.004517', '-0.262', '0.1729', '0.46', '0.11127', '0.307', '-0.2512', '0.4507', '-0.01591', '-0.05176', '0.149', '0.536', '-0.376', '0.3105', '-0.0008492', '0.801', '0.3984', '-0.3914', '0.1758', '-0.822', '-0.1198', '0.2913']",C40553,,C536736,,,,
mondo:0008583,inherited torticollis,"['inherited torticollis (disease)', 'torticollis, familial', 'familial torticollis', 'familial spasmodic torticollis', 'fibromatosis colli', 'congenital muscular torticollis', 'torticollis, congenital', 'torticollis']",,189600,,,,C4811,,C535425,723.5,,,0000473
mondo:0008584,torus palatinus and torus mandibularis,['torus palatinus and torus mandibularis'],,189700,,C1861044,,,,C566043,,,,
mondo:0008585,HELLP syndrome,"['hemolysis, elevated liver enzymes, low platelets in pregnancy', 'hemolysis, elevated liver enzymes, and low platelet count', 'hypertension, pregnancy-induced', 'PREG1', 'PEE1', 'hemolysis, elevated liver enzymes, lowered platelets', 'toxemia of pregnancy', 'hemolysis-elevated liver enzymes-low platelet count syndrome', 'toxaemia of pregnancy', 'PREECLAMPSIA/eclampsia 1', 'hemolysis-elevated liver enzymes-low platelets syndrome']",13133,,244242,C0162739,,C84750,0007297,D017359,,,10049058,
mondo:0008586,esophageal atresia/tracheoesophageal fistula,"['te fistula', 'tracheoesophageal fistula', 'tracheoesophageal fistula with or without esophageal atresia', 'TEF', 'esophageal atresia with or without tracheoesophageal fistula', 'esophageal atresia and/or tracheoesophageal fistula', 'tracheoesophageal fistula with or without esohageal atresia']",0080171,189960,1199,,,,,D004933,,,10030146,
mondo:0008587,tracheobronchopathia osteochondroplastica,"['tracheopathia osteoplastica', 'tracheobronchopathia osteoplastica', 'cartilaginous or bony projections into the tracheobronchial lumen', 'tracheobronchopathia osteochondroplastica']",,189961,3348,CN204359,,,,C536977,,,,
mondo:0008588,hereditary geniospasm,"['trembling Chin', 'GSM1', 'geniospasm', 'geniospasm 1', 'GSM 1', 'hereditary chin myoclonus', 'familial trembling of the chin', 'hereditary chin-trembling', 'hereditary chin tremor/myoclonus']",,190100,53372,C2931589,,,,C537682,,,,
mondo:0008589,"tremor of intention, ataxia, and lipofuscinosis","['tremor of intention, ataxia, and lipofuscinosis']",,190200,,C1860872,,,,C566038,,,,
mondo:0008590,"tremor, hereditary essential, 1","['FET1', 'tremor hereditary essential, 1', 'tremor, hereditary essential, 1', 'tremor, familial essential, 1', 'tremor, hereditary essential, type 1', 'tremor familial essential, 1', 'DRD3 essential tremor', 'essential tremor, hereditary, 1', 'ETM1', 'essential tremor caused by mutation in DRD3']",0111428,190300,,C1860861,,,,C536545,,,,
mondo:0008591,tremor-nystagmus-duodenal ulcer syndrome,"['tremor, NYSTAGMUS, and duodenal ulcer', 'Neuhauser Daly Magnelli syndrome', 'tremor nystagmus duodenal ulcer', 'Neuhauser-Daly-Magnelli syndrome']",,190310,3350,C1860860,,,,C536406,,,,
mondo:0008592,tricho-dento-osseous syndrome,"['TRICHODENTOOSSEOUS syndrome', 'Tricho-dento-osseous syndrome 1', 'TDO syndrome', 'TDO syndrome 1', 'TDO', 'enamel hypoplasia and hypocalcification with associated strikingly curly hair', 'trichodontoosseous syndrome', 'kinky or curly hair, dolichocephaly, enamel hypoplasia, increased dental caries, radial dense bones, and brittle nails']",0111565,190320,3352,,"['0.10016', '0.1559', '-0.1138', '-0.144', '0.2278', '0.1372', '0.2673', '1.124', '-0.2379', '-0.229', '-0.524', '-0.02757', '-0.1443', '0.00816', '0.4324', '0.04092', '0.6606', '-0.001663', '-0.3594', '-0.861', '0.2019', '-0.02634', '0.598', '-0.3813', '-0.04028', '0.04172', '-0.5107', '0.2573', '0.313', '-0.2822', '0.6216', '-0.5176', '-0.1941', '0.3464', '0.5815', '-0.03336', '-0.5522', '-0.391', '0.05814', '-0.2893', '0.11707', '-0.03119', '0.1481', '-0.7407', '-0.3108', '-0.3677', '0.6626', '0.10645', '-0.1063', '-0.1826', '0.2162', '-0.2338', '0.1276', '-0.00217', '-0.625', '-0.7144', '0.1423', '-0.2646', '0.283', '-0.3257', '0.1587', '0.1357', '-0.685', '-0.2646', '0.2175', '0.289', '0.1459', '0.629', '-0.63', '0.6636', '0.2075', '-0.01904', '0.0945', '0.004143', '0.293', '-0.307', '-0.2216', '-0.4058', '-0.0869', '-0.4727', '-0.04376', '0.02461', '0.3762', '0.4421', '-0.2815', '0.06555', '0.1108', '0.1365', '0.481', '-0.4812', '-0.465', '0.12366', '-0.196', '0.2168', '0.1981', '0.04785', '0.5156', '-0.05267', '0.1578', '-0.648']",,,C536549,759.89,,,
mondo:0008593,trichomegaly,"['trichomegaly', 'eyelashes, long', 'TCMGLY']",,190330,,,"['-0.01596', '0.03038', '0.0141', '-0.012825', '0.0005355', '-0.03262', '0.014114', '0.02184', '-0.02505', '-0.01343', '-0.01575', '-0.01343', '-0.01692', '0.01508', '-0.00827', '-0.02542', '-0.002182', '-0.01868', '-0.01938', '-0.0598', '0.003597', '-0.02089', '0.0276', '-0.01117', '0.01297', '-0.01653', '-0.02309', '-0.002035', '0.01535', '-0.02469', '0.02568', '-0.01312', '0.02382', '0.01411', '0.000623', '-0.0357', '-0.01715', '-0.002653', '-0.004086', '-0.03314', '0.0005603', '-0.02014', '0.00596', '-0.01316', '-0.01112', '-0.0435', '0.01057', '0.02216', '0.00569', '0.00939', '-0.01785', '-0.0034', '-0.01181', '0.004265', '-0.0208', '-0.00872', '0.03662', '-0.02023', '-0.05325', '0.00753', '0.00974', '0.01521', '-0.01819', '0.01826', '0.006916', '-0.013054', '0.0327', '0.02344', '-0.02333', '0.03372', '-0.03598', '0.007168', '0.01427', '-0.03458', '0.001102', '0.01018', '-0.005375', '-0.0052', '-0.01235', '-0.01189', '-0.00881', '-0.005802', '0.004864', '0.03096', '-0.007473', '-0.01402', '0.008', '0.02194', '0.03958', '0.008575', '0.01277', '0.02187', '-0.00975', '0.01086', '0.07935', '0.03473', '0.0377', '-0.0535', '-0.000783', '0.01994']",,,,,,,
mondo:0008594,familial multiple discoid fibromas,"['hereditary multiple trichodiscomas', 'small benign fibrovascular tumour of the dermal part of the hair disc', 'trichodiscomas, familial multiple', 'FMDF', 'discoid fibromas, familial multiple', 'small benign fibrovascular tumor of the dermal part of the hair disk', 'familial multiple trichodiscomas']",,190340,538756,C1860850,,,,C536847,,,,
mondo:0008595,"trichoepitheliomas, multiple desmoplastic","['trichoepitheliomas, multiple desmoplastic']",,190345,,C1860849,,,,C566034,,,,
mondo:0008596,trichorhinophalangeal syndrome type I,"['trichorhinophalangeal syndrome, type I', 'type I trichorhinophalangeal syndrome', 'Sugio-Kajii syndrome', 'trichorhinophalangeal dysplasia type I', 'Giedion syndrome', 'TRPS1', 'trichorhinophalangeal syndrome type 1', 'TRPS 1', 'trichorhinophalangeal syndrome, type 1', 'type III trichorhinophalangeal syndrome']",14743,190350,,,"['-0.00947', '0.0448', '0.004105', '-0.003214', '0.02443', '-0.04477', '-0.005707', '0.05484', '-0.04144', '-0.02315', '-0.02322', '-0.0112', '0.006123', '0.01598', '-0.04004', '-0.02655', '0.01197', '-0.01566', '-0.013374', '-0.09125', '-0.00706', '-0.01327', '0.0702', '-0.00793', '0.01348', '0.001782', '-0.0215', '-0.01697', '0.015274', '-0.03378', '0.02826', '0.00243', '0.04883', '0.02486', '-0.007603', '-0.027', '-0.008766', '-0.03766', '0.002611', '-0.05762', '0.01746', '-0.0449', '0.01372', '-0.015236', '-0.006157', '-0.04932', '0.000755', '0.0419', '0.0242', '0.01833', '-0.000729', '-0.02472', '0.0001876', '-0.010925', '-0.02504', '-0.01712', '0.0345', '-0.013664', '-0.04785', '0.010284', '0.01439', '0.019', '0.01072', '0.003635', '-0.013504', '0.003252', '0.04517', '0.0464', '-0.05725', '0.0633', '-0.04117', '-0.00347', '0.01816', '-0.03696', '0.02574', '0.04413', '-0.01906', '-0.006866', '-0.03574', '-0.01084', '-0.002642', '-0.002905', '-0.03458', '0.03134', '-0.02463', '0.0051', '0.03204', '0.06976', '0.071', '0.01194', '0.012665', '0.04514', '0.007607', '0.01813', '0.0926', '0.04068', '0.0502', '-0.07623', '-0.001195', '0.01002']",C75109,,C536820,759.89,,,
mondo:0008597,"trichorhinophalangeal syndrome, type III","['trichorhinophalangeal syndrome, type 3', 'TRPS 3', 'Sugio-Kajii syndrome', 'trichorhinophalangeal syndrome type 3', 'TRPS3', 'trichorhinophalangeal syndrome, type III']",0080376,190351,,C1860823,,,,C566033,,,,
mondo:0008598,trichodysplasia-xeroderma syndrome,"['trichodysplasia-xeroderma', 'trichodysplasia xeroderma']",,190360,3361,C1860822,,,,C566032,,,,
mondo:0008599,trigeminal neuralgia,"['trigeminal neuralgia', 'trifacial neuralgia', 'neuralgia of trigeminal nerve', 'trifocal neuralgia', 'trigeminal nerve neuralgia', 'Tic douloureux']",12098,190400,221091,C0040997,,,1001219,D014277,350.1,G50.0,10044652,
mondo:0008600,trigger thumb,"['trigger thumb', 'congenital trigger thumb (type)', 'bilateral trigger thumb (type)', 'recurrent trigger thumb (type)']",,190410,,C0158328,,,,D052582,,,,
mondo:0008601,"triglyceride storage disease, type 1","['triglyceride storage disease, type I']",,190420,,C1860821,,,,C566031,,,,
mondo:0008602,"triglyceride storage disease, type 2","['triglyceride storage disease, type II']",,190430,,C1860820,,,,C566030,,,,
mondo:0008603,trigonocephaly 1,"['trigonocephaly 1', 'FGFR1 isolated trigonocephaly', 'trigonocephaly type 1', 'isolated trigonocephaly caused by mutation in FGFR1', 'TRIGNO1', 'craniosynostosis, metopic']",,190440,,,,,,,,,,
mondo:0008604,triphalangeal thumb with double phalanges,['triphalangeal thumb with double phalanges'],,190500,,C1860807,,,,C566028,,,,
mondo:0008605,"triphalangeal thumb, Nonopposable","['triphalangeal thumb non opposable', 'triphalangeal thumb, Nonopposable', 'TPT', 'non-opposable triphalangeal thumb']",,190600,,C2931238,,,,C536562,,,,
mondo:0008606,Say-field-Coldwell syndrome,"['polydactyly with triphalangeal thumbs, brachydactyly, camptodactyly, congenital dislocation of the patellas, short stature and borderline intelligence', 'triphalangeal thumbs-dislocation of patella syndrome', 'triphalangeal thumbs and dislocation of patella']",,190650,3133,C1860805,,,,C536619,,,,
mondo:0008607,triphalangeal thumbs-brachyectrodactyly syndrome,"['Carnevale-Hernández-del Castillo syndrome', 'triphalangeal thumb and brachyectrodactyly syndrome', 'triphalangeal thumbs brachyectrodactyly', 'triphalangeal thumb and brachy-ectrodactyly syndrome', 'triphalangeal thumbs with brachyectrodactyly']",,190680,2947,C1860804,,,,C536564,,,,
mondo:0008608,Down syndrome,"['transient myeloproliferative disorder of Down syndrome', 'Downs syndrome', 'trisomy 21', 'complete trisomy 21 syndrome', 'trisomy 21 (Down syndrome)', 'trisomy 21 syndrome', 'Down syndrome, Isolated cases', 'Down syndrome', 'Down syndrome chromosome region', 'leukemia, megakaryoblastic, of Down syndrome', 'G trisomy', 'Down syndrome critical region', 'Down^s syndrome - trisomy 21', 'leukemia, megakaryoblastic, with or without Down syndrome, somatic', 'Down^s syndrome']",14250,190685,870,C0013080,,C2993,0001064,D004314,758.0,,10044688,
mondo:0008609,Tristichiasis,"['eyelashes, three rows of', 'Tristichiasis']",,190800,,,,,,,,,,
mondo:0008610,blue color blindness,"['congenital tritanopia', 'tritanopia', 'blue colorblindness', 'tritan color blindness', 'colorblindness, tritan', 'blue color blindness', 'colorblindness, tritanopic', 'tritan defect', 'tritan colour blindness']",11661,190900,88629,C0155017,"['-0.179', '-0.522', '0.6963', '0.1354', '-0.0701', '0.1328', '-0.2253', '-0.015015', '-0.749', '-0.3645', '0.851', '-0.1508', '-0.444', '0.273', '0.429', '-0.535', '0.10333', '0.446', '-0.5674', '-0.08905', '-0.8965', '-0.10864', '-0.0605', '-0.1785', '0.05878', '-0.4875', '-0.264', '-0.0811', '0.0432', '0.2837', '0.464', '-0.1378', '0.514', '0.7563', '-0.2272', '-0.179', '-0.2737', '-0.728', '0.2888', '-0.6743', '0.4597', '-0.474', '-0.1925', '-0.3657', '0.0636', '-0.1936', '0.10547', '-0.1989', '0.985', '0.2869', '0.4204', '0.379', '0.661', '-0.4846', '0.04703', '0.148', '0.1854', '0.1775', '-0.6294', '0.002197', '-0.4448', '-0.133', '0.9976', '0.951', '0.1459', '-0.0129', '0.8384', '0.831', '-0.2485', '0.5645', '0.1638', '0.2603', '-0.1696', '-0.5825', '-0.1192', '0.381', '0.3145', '0.22', '0.2072', '-0.2297', '0.4653', '-0.2725', '0.2155', '0.868', '0.1719', '-0.4116', '0.4727', '-0.4712', '0.7075', '0.6416', '0.1236', '0.3079', '0.01639', '0.2278', '0.7163', '0.3508', '-0.5073', '-0.4016', '0.01122', '-0.3247']",,,,368.53,,,
mondo:0008611,humerus trochlea aplasia,"['trochlea of the HUMERUS, aplasia OF', 'trochlea of the humerus aplasia of', 'aplasia of trochlea of the humerus']",,191000,3383,C1860773,,,,C566022,,,,
mondo:0008612,tuberous sclerosis 1,"['tuberous sclerosis, type 1', 'TSC1', 'tuberose sclerosis', 'TSC1 tuberous sclerosis', 'tuberous sclerosis Complex', 'tuberous sclerosis caused by mutation in TSC1', 'tuberous sclerosis-1', 'tuberous sclerosis type 1', 'tuberous sclerosis 1']",0080324,191100,,,,C75122,,C565346,,,,
mondo:0008613,Tuftsin deficiency,['Tuftsin deficiency'],,191150,,C0398741,,,,C562872,279.03,,,
mondo:0008614,suppressor of tumorigenicity 3,"['tumor-suppressor Gene, Hela cell type', 'suppressor of tumorigenicity 3', 'cervical carcinoma', 'cervical carcinoma, tumor-suppressor Gene involved 1N', 'ST3']",,191181,,C1860658,,,,,,,,
mondo:0008615,tune deafness,"['tone deafness', 'Dysmelodia', 'amusia, congenital', 'tune deafness']",,191200,,C1860646,,,,C566019,389.8,,,
mondo:0008617,inflammatory bowel disease 11,"['inflammatory bowel disease type 11', 'inflammatory bowel disease 11', 'IBD11']",0110894,191390,,C2674051,,,,C567154,,,,
mondo:0008618,"mesomelic dwarfism, Reinhardt-Pfeiffer type","['Reinhardt-Pfeiffer mesomelic dysplasia', 'mesomelic dwarfism of hypoplastic ulna and fibula type', 'hypoplasia of ulna and fibula', 'ulna and fibula, hypoplasia OF', 'Reinhardt-Pfeiffer syndrome', 'mesomelic dysplasia Reinhardt-Pfeiffer type']",,191400,2634,C1860616,,,,C537349,,,,
mondo:0008619,ulna metaphyseal dysplasia syndrome,"['Rosenberg-Lohr syndrome', 'metaphyseal chondroplasia Rosenberg type', 'metaphyseal chondrodysplasia, Rosenberg type', 'Rosenberg Lohr syndrome', 'hereditary bone dysplasia with characteristic bowing and thickening of the distal ulna', 'ulna metaphyseal dysplasia syndrome']",,191420,1837,C1860615,,,,C536935,,,,
mondo:0008620,upper limb mesomelic dysplasia,"['upper limb mesomelic dysplasia', 'ulna hypoplasia', 'Fryns-Hofkens-Fabry syndrome', 'Fryns Hofkens Fabry syndrome', 'ulnar hypoplasia']",,191440,2497,,,,,C538069,,,,
mondo:0008621,uncombable hair syndrome,"['cheveux incoiffables', 'spun glass hair', 'uncombable hair syndrome', 'pili trianguli et canaliculi', 'unmanageable hair syndrome']",,,1410,C0432347,"['0.0097', '-0.2474', '-0.2333', '0.5186', '0.447', '-0.283', '-0.1451', '0.3977', '0.1881', '0.1306', '-0.4282', '0.2961', '-0.1802', '-0.1436', '-0.04477', '0.006813', '0.2097', '-0.4695', '-0.1674', '-0.751', '-0.1765', '0.03976', '-0.05487', '-0.311', '0.2372', '-0.02808', '-0.793', '-0.013466', '-0.2391', '-0.1458', '0.3647', '-0.1349', '-0.1725', '0.1489', '0.1593', '0.4014', '0.01982', '-0.2036', '-0.03333', '-0.4043', '0.3782', '0.08734', '-0.0821', '-0.5864', '0.03876', '-0.1891', '-0.2825', '0.3176', '-0.194', '-0.4739', '0.0346', '0.02885', '0.446', '0.1289', '0.2499', '0.04233', '0.3345', '-0.251', '-0.5957', '-0.1257', '0.024', '-0.1449', '-0.1693', '-0.163', '0.2874', '-0.2244', '0.759', '0.3079', '-0.02414', '0.5854', '-0.2346', '-0.2817', '-0.1348', '0.06714', '0.03323', '-0.2374', '-0.3657', '-0.5776', '-0.2715', '-0.607', '0.3596', '0.08673', '-0.01602', '0.1018', '0.003609', '0.08813', '-0.0624', '0.5254', '0.6855', '0.1083', '-0.038', '0.4114', '-0.10425', '0.7266', '0.4084', '-0.3313', '0.2286', '-0.266', '0.3328', '0.2905']",,,C536939,,,,
mondo:0008622,tricho-retino-dento-digital syndrome,"['Bork syndrome', 'uncombable hair, retinal pigmentary dystrophy, dental anomalies, and brachydactyly', 'uncombable hair-retinal pigmentary dystrophy-dental anomalies-brachydactyly syndrome', 'Bork Stender Schmidt syndrome']",,191482,1264,C1860605,,,,C536576,,,,
mondo:0008623,Undritz anomaly,"['hypersegmentation of nuclei of polymorphonuclear leukocytes', 'Undritz anomaly']",,191500,,C1860604,,,,C566014,,,,
mondo:0008624,Upington disease,"['Upington disease', 'Perthes-like hip disease, enchondromata, and Ecchondromata', 'familial dyschondroplasia', 'hip dysplasia-enchondromata-ecchondroma syndrome']",,191520,3408,C1860596,,,,C536472,,,,
mondo:0008626,"ureter, bifid or double","['ureter, bifid or double']",,191550,,C1860586,,,,C566012,,,,
mondo:0008627,ureter cancer,"['ureter, cancer OF', 'malignant tumor of the ureter', 'cancer of ureter', 'ureter cancer', 'malignant tumour of the ureter', 'malignant ureter tumor', 'malignant neoplasm of ureter', 'malignant ureteral tumour', 'malignant tumour of ureter', 'malignant ureteral tumor', 'malignant tumor of ureter', 'malignant ureter neoplasm', 'malignant neoplasm of the ureter', 'malignant ureter tumour', 'malignant ureteral neoplasm']",11819,191600,,C0153619,,C7543,,D014516,189.2,C66,,
mondo:0008628,ureterocele,"['ureterocele (disease)', 'ureterocele']",4022,191650,,,,C123159,1001227,D014518,593.89,,10056433,0000070
mondo:0008629,"urolithiasis, uric acid, autosomal dominant","['urolithiasis, uric acid, autosomal dominant', 'nephrolithiasis, uric acid, autosomal dominant']",0080654,191700,,,,,,,,,,
mondo:0008630,"urinary bladder, atony of","['atony of urinary bladder', 'bladder dysfunction, autonomic, with impaired pupillary reflex and secondary CAKUT', 'urinary bladder, atony of']",,191800,,,,,,,,,,
mondo:0008632,"urticaria, aquagenic","['aquagenic urticaria', 'urticaria, aquagenic']",,191850,,C0263334,,,,C562481,708.8,,,
mondo:0008633,Muckle-Wells syndrome,"['MUCKLE-Wells syndrome', 'Uda syndrome', 'Muckle-Wells syndrome', 'urticaria, deafness and amyloidosis', 'neutrophilic urticaria', 'Cryopyrin-associated periodic syndrome 2', 'urticaria-deafness-amyloidosis syndrome', 'MWS', 'Muckle Wells syndrome']",0050854,191900,575,C1304205,"['0.339', '0.1412', '-0.2395', '0.2515', '0.01413', '-0.4397', '-0.03174', '0.62', '0.00645', '0.04538', '-0.6997', '0.2495', '-0.3052', '0.1954', '-0.7563', '0.09064', '0.5166', '0.347', '0.4475', '-0.501', '0.33', '-0.391', '0.2461', '-0.2734', '0.1711', '0.2612', '-0.1376', '0.2864', '-0.1595', '0.07153', '0.0824', '-0.05692', '0.517', '0.321', '-0.1158', '-0.03723', '-0.461', '-0.358', '-0.4607', '0.4246', '0.03275', '-0.501', '0.3557', '0.0747', '0.1383', '0.4258', '-0.4453', '0.08813', '0.8633', '0.7124', '-0.10767', '0.379', '0.1909', '-0.522', '0.301', '-0.2158', '0.5986', '-0.4324', '-0.2932', '-0.2393', '0.08417', '0.529', '-0.3281', '-0.2097', '0.2098', '0.2004', '0.00988', '0.9565', '0.1316', '0.3242', '-0.09863', '0.1161', '0.06506', '-0.00934', '0.2396', '0.2006', '0.3435', '0.4197', '0.00882', '0.0686', '-0.001381', '-0.1863', '-0.2266', '0.2432', '0.532', '-0.04202', '0.3364', '0.86', '-0.2717', '0.2751', '0.542', '0.283', '0.5776', '0.2383', '0.961', '0.0258', '0.388', '-0.2406', '0.1613', '-0.2898']",C119054,,,708.8,,10064569,
mondo:0008634,"urticaria, familial localized heat","['urticaria, familial localized heat']",,191950,,C1860551,,,,C566011,,,,
mondo:0008635,uterine anomalies,['uterine anomalies'],,192000,,,,,,C562565,,,,
mondo:0008636,double uterus-hemivagina-renal agenesis syndrome,"['OHVIRA syndrome', 'uterus BICORNIS BICOLLIS with partial vaginal septum and unilateral HEMATOCOLPOS with ipsilateral renal agenesis', 'Wunderlich syndrome', 'Double uterus and obstructed hemivagina syndrome', 'Herlyn-Werner syndrome', 'obstructed hemivagina and ipsilateral renal anomaly']",,192050,3411,,,,,C566010,,,,
mondo:0008637,bifid uvula,"['uvular cleft', 'bifidity of the uvula', 'uvula, cleft', 'uvula, bifid']",,192100,99771,,,,,,,,,
mondo:0008638,varicose disease,"['varix', 'varices', 'varicose veins', 'Venous varices', 'Venous ectasia']",799,192200,,C0042345,,C35114,,D014648,456.8,,,
mondo:0008639,vascular helix of umbilical cord,['vascular helix of umbilical cord'],,192300,,,,,,,,,,
mondo:0008640,"vasculitis, lymphocytic, nodular","['vasculitis lymphocytic, nodular', 'vasculitis, lymphocytic, nodular', 'lymphocytic vasculitis']",,192310,,C1860519,,,,C566008,,,,
mondo:0008641,retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations,"['HVR', 'ADRVCL', 'grand Kaine fulling syndrome', 'grand-Kaine-fulling syndrome', 'retinal vasculopathy with cerebral leukodystrophy', 'vasculopathy, retinal, with cerebral leukoencephalopathy and systemic manifestations', 'CRV', 'autosomal dominant retinal vasculopathy with cerebral leukodystrophy', 'cerebroretinal vasculopathy, hereditary', 'RVCL', 'hereditary vascular retinopathy', 'retinal vasculopathy and cerebral leukoencephalopathy', 'RVCL-S', 'cerebroretinal vasculopathy', 'retinopathy, vascular, with cerebral and renal involvement and Raynaud and migraine phenomena', 'vasculopathy, retinal, with cerebral leukodystrophy']",0111567,192315,247691,C1860518,"['0.129', '0.0422', '0.3425', '-0.4006', '-0.1427', '-0.4133', '-0.1166', '-0.10876', '-0.1121', '0.11255', '-0.03047', '-0.6978', '0.0236', '-0.095', '-0.1478', '-0.774', '-0.0868', '-0.0215', '0.4465', '-0.2708', '0.3518', '-0.2566', '0.2484', '0.2198', '0.0398', '0.1493', '-0.2423', '-0.1388', '0.1707', '0.2455', '0.08685', '0.0626', '0.691', '0.2406', '0.4836', '-0.0701', '-0.0754', '-0.1018', '-0.4004', '-0.7637', '0.1501', '-0.935', '0.4548', '-0.501', '0.3677', '-0.2798', '-0.04663', '0.4197', '0.2676', '0.2302', '0.8853', '1.094', '-0.1151', '-0.582', '0.11475', '-0.1153', '0.6147', '-0.06226', '-0.739', '0.3118', '-0.3323', '0.0815', '0.268', '-0.03125', '-0.06213', '-0.2205', '0.2168', '0.831', '-0.309', '0.594', '-0.1995', '0.117', '0.3445', '-0.2096', '0.345', '0.2898', '0.397', '0.2253', '-0.5015', '-0.04092', '-0.452', '-0.07495', '-0.227', '0.603', '-0.3208', '-0.3767', '0.3262', '0.007442', '0.339', '-0.3862', '0.7285', '0.2319', '0.09686', '0.2124', '0.263', '0.1942', '0.4395', '0.0652', '-0.04044', '0.4075']",,,C566007,,,,
mondo:0008642,VACTERL/vater association,"['vertebral abnormalities, anal atresia, Cardiac abnormalities, tracheo-esophageal fistula, renal anomalies, limb defects syndrome', 'VATER/VACTERL association', 'VATER association', 'VACTERL association', 'VATER syndrome']",14679,192350,887,CN206312,"['0.4263', '-0.1815', '-0.1532', '-0.542', '0.1364', '-0.48', '0.2386', '0.932', '-0.7725', '-0.5586', '-0.1979', '-0.12024', '-0.0409', '0.441', '-0.5083', '-0.1245', '-0.4126', '-0.4185', '-0.796', '-0.5845', '0.768', '0.3684', '1.031', '0.04483', '0.5195', '-0.149', '-0.364', '0.5996', '0.3848', '-0.2773', '0.553', '-0.6514', '0.0119', '0.2654', '0.4136', '-0.06155', '-0.1337', '-0.29', '-0.3706', '0.381', '0.165', '-0.2544', '0.2966', '-0.754', '0.582', '-0.3481', '0.2898', '0.1926', '-0.594', '0.09143', '-0.5176', '-0.4', '0.1459', '-0.9097', '-0.652', '-0.3174', '0.4487', '0.1901', '-0.826', '-0.0761', '-0.001202', '-0.1533', '0.01507', '-0.02292', '-0.0895', '-0.3362', '0.4006', '-0.1846', '-0.738', '0.1971', '-0.0788', '0.0917', '-0.2505', '0.04077', '0.2036', '-0.1414', '0.3176', '-0.307', '-0.4268', '0.03302', '0.05527', '0.1925', '0.149', '0.2502', '-0.4888', '-0.1906', '0.6304', '0.3506', '-0.3005', '-0.5317', '0.28', '-0.3162', '0.1691', '-0.02405', '0.676', '-0.336', '0.3323', '-0.4126', '-0.1332', '-0.2964']",C99105,,,759.89,,10066022,
mondo:0008643,"veins, pattern of, on anterior thorax","['veins, pattern of, on anterior thorax']",,192400,,,,,,,,,,
mondo:0008644,velocardiofacial syndrome,"['VCF syndrome', 'Shprintzen syndrome', 'VCF-velocardiofacial syndrome', 'deletion 22q11.2 syndrome', 'velocardiofacial syndrome', 'Shprintzen VCF syndrome', 'chromosome 22Q11.2 deletion syndrome', '22q11 deletion syndrome']",12583,192430,,CN205308,,,,D004062,758.32,,,
mondo:0008645,ventricular extrasystoles with syncopal episodes-perodactyly-robin sequence syndrome,"['ventricular extrasystoles perodactyly Robin sequence', 'ventricular extrasystoles with syncopal episodes - perodactyly - Robin sequence', 'Stoll-Kieny-Dott syndrome', 'ventricular extrasystoles with syncope, perodactyly, and ROBIN sequence']",,192445,3201,,,,,C537497,,,,
mondo:0008647,hypertrophic cardiomyopathy 1,"['CMH1', 'MYH7 hypertrophic cardiomyopathy', 'cardiomyopathy, familial hypertrophic, 1', 'hypertrophic cardiomyopathy type 1', 'Cmh', 'hypertrophic subaortic stenosis, idiopathic', 'ventricular Hypertrophy, hereditary', 'cardiomyopathy, hypertrophic, 1, Autosomal dominant, Digenic dominant', 'asymmetric septal Hypertrophy', 'cardiomyopathy, familial hypertrophic, Autosomal dominant, Digenic dominant', 'cardiomyopathy, familial hypertrophic, type 1', 'hypertrophic cardiomyopathy caused by mutation in MYH7', 'cardiomyopathy, familial hypertrophic 1', 'cardiomyopathy, hypertrophic, 1, digenic, Autosomal dominant, Digenic dominant']",0110307,192600,,,,,,,,,,
mondo:0008648,"ventricular tachycardia, familial","['hereditary ventricular tachycardia', 'ventricular tachycardia, idiopathic', 'familial ventricular tachycardia', 'ventricular tachycardia, familial polymorphic', 'ventricular tachycardia, familial']",,192605,,,,,,,,,,
mondo:0008649,"venular insufficiency, systemic","['venular insufficiency, systemic']",,192700,,C1860465,,,,C566004,,,,
mondo:0008650,posterior fusion of lumbosacral vertebrae-blepharoptosis syndrome,"['Faulk Epstein Jones syndrome', 'Faulk-Epstein-Jones syndrome', 'congenital ptosis and posterior fusion of lumbosacral vertebrae', 'familial posterior lumbosacral vertebral fusion and eyelid ptosis', 'vertebral fusion, POSTERIOR lumbosacral, with blepharoptosis', 'vertebral fusion posterior lumbosacral blepharoptosis']",,192800,2064,C1860464,,,,C536344,,,,
mondo:0008651,vertebral hypoplasia with lumbar kyphosis,['vertebral hypoplasia with lumbar kyphosis'],,192900,,C1860463,,,,C566002,,,,
mondo:0008652,congenital vertical talus,"['CVT', 'pes valgus, congenital convex', 'rocker bottom foot', 'rocker-bottom foot deformity', 'Charcot-Marie-Tooth disease, foot deformity of', 'vertical talus', 'congenital convex pes valgus', 'rocker-bottom foot', 'vertical talus, congenital', 'congenital rocker-bottom foot', 'congenital convex foot']",0111568,192950,178382,,"['-0.383', '-0.2306', '-0.2042', '0.127', '0.5703', '-0.299', '0.1247', '0.4133', '-0.5815', '-0.4941', '0.06824', '0.1802', '0.1335', '0.243', '-0.2925', '0.1444', '0.3596', '-0.1915', '-0.1559', '-0.4917', '-0.3298', '0.2554', '0.4265', '-0.1823', '0.1683', '0.1309', '-0.4004', '-0.09906', '0.0479', '-0.04498', '-0.09314', '-0.1603', '0.0712', '0.289', '0.08813', '-0.2727', '-0.01342', '-0.3364', '-0.01238', '-0.2494', '0.0724', '-0.266', '-0.05325', '0.127', '-0.0443', '0.0861', '-0.1137', '0.2769', '0.1054', '-0.1083', '0.12463', '-0.4363', '0.01416', '-0.02582', '-0.47', '-0.3152', '0.4006', '-0.1831', '-0.1212', '-0.215', '0.607', '0.03262', '-0.1677', '0.4888', '-0.1945', '0.1465', '0.2283', '0.2399', '-0.07916', '0.04932', '-0.00151', '0.2052', '0.2108', '-0.07245', '0.07074', '-0.04324', '0.03117', '0.11835', '-0.379', '-0.3926', '-0.307', '-0.266', '0.2338', '0.7593', '-0.1736', '0.1344', '-0.1512', '0.1545', '0.2847', '0.02869', '-0.2263', '0.3347', '-0.0903', '0.3333', '0.563', '-0.0334', '0.398', '-0.4304', '0.3394', '0.063']",,,C536345,755.67,,10066242,
mondo:0008653,vesicoureteral reflux 1,"['Vesicoureteral reflux', 'vesicoureteral reflux 1', 'VUR', 'VUR1']",,193000,,CN032731,,,,,,,,
mondo:0008654,"nystagmus 4, congenital, autosomal dominant","['vestibulocerebellar disorder with predominant ocular signs', 'NYS4', 'NYSTAGMUS 4, congenital, autosomal dominant']",,193003,,,,,,C537856,,,,
mondo:0008655,"vestibulocochlear dysfunction, progressive","['familial progressive vestibulocochlear dysfunction', 'vestibulocochlear dysfunction, progressive']",,193005,,C2931176,,,,C536346,,,,
mondo:0008659,transcobalamin I deficiency,"['transcobalamin 1 deficiency', 'transcobalamin-1 deficiency', 'transcobalamin I deficiency', 'cobalamin Pseudodeficiency due to transcobalamin deficiency', 'cobalamin R Binder Protein deficiency', 'Tcn1 deficiency', 'R Binder deficiency with lactoferrin deficiency', 'Haptocorrin deficiency', 'transcobalamin 1 deficiency with lactoferrin deficiency', 'TCI deficiency']",,193090,2967,C0342700,,,,C562798,,,,
mondo:0008660,autosomal dominant hypophosphatemic rickets,"['vitamin D-resistant rickets, autosomal dominant', 'ADHR', 'autosomal dominant hereditary hypophosphatemic rickets', 'hypophosphatemia, autosomal dominant', 'hereditary hypophosphatemic rickets, autosomal dominant', 'hypophosphatemic rickets, autosomal dominant', 'autosomal dominant hypophosphatemia']",0050948,193100,89937,C0342642,"['0.659', '-0.1338', '0.2267', '-0.1051', '-0.03665', '-0.1982', '-1.093', '1.325', '-0.4128', '-0.0311', '0.4292', '0.627', '-0.7183', '1.09', '-0.4834', '0.1841', '-0.1552', '0.2096', '-0.8125', '-0.8735', '-0.2339', '-1.08', '0.3264', '-0.4023', '0.0763', '-0.372', '0.07935', '-0.41', '0.1152', '-0.1276', '0.12396', '-0.4343', '-0.4277', '0.3079', '-0.09033', '-0.2251', '-0.09235', '-0.06195', '0.67', '0.1337', '-0.1526', '-0.0863', '-0.578', '-0.274', '0.233', '-0.328', '0.2908', '-0.1002', '0.1862', '0.5103', '-0.2184', '-0.76', '0.1866', '0.1098', '-0.4578', '-0.519', '-0.3345', '-0.01139', '-0.916', '0.009995', '0.593', '-0.2496', '-0.616', '0.5103', '0.3208', '0.7954', '1.093', '1.291', '-0.484', '-0.669', '0.6187', '-0.1595', '0.4177', '-0.4731', '0.2515', '0.908', '0.014114', '-0.808', '0.6577', '0.04346', '0.213', '0.252', '0.5825', '-0.1995', '-0.0771', '0.1696', '0.368', '0.08673', '0.752', '0.653', '0.4944', '-0.2191', '-0.5513', '-0.0841', '-0.3535', '0.2751', '0.8975', '-0.09625', '-0.4614', '-0.3076']",,,C562791,,E83.3,,
mondo:0008661,vitiligo,,12306,,247871,C0042900,"['0.2732', '0.1982', '0.2013', '0.3706', '0.1169', '-0.3728', '0.1582', '0.1317', '-0.9995', '-0.0873', '0.04398', '0.1686', '-0.2634', '-0.007935', '0.004017', '0.2268', '0.2776', '-0.6694', '0.05222', '-0.481', '-0.3735', '-0.3955', '0.518', '-0.4265', '0.303', '0.0547', '-0.336', '0.1381', '-0.2413', '0.66', '0.2103', '-0.2261', '-0.09564', '-0.455', '0.544', '0.5376', '-0.943', '0.1306', '0.05542', '0.1161', '0.3196', '0.01974', '-0.03192', '-0.1785', '0.1044', '-0.2278', '-0.107', '-0.2344', '0.3425', '-0.204', '0.04718', '-0.0891', '0.8047', '-0.1357', '-0.1793', '0.2019', '0.1947', '0.02136', '-0.7544', '-0.763', '-0.2479', '-0.45', '-0.01875', '0.08246', '-0.1709', '0.579', '0.6343', '0.9194', '0.11774', '0.9365', '0.2024', '0.408', '-0.3447', '-0.2715', '-0.2722', '0.5264', '-0.1635', '0.3547', '-0.09155', '-0.435', '0.3103', '-0.128', '-0.1738', '-0.2247', '-0.10626', '-0.712', '-0.1548', '0.1798', '0.6514', '0.3997', '0.261', '0.234', '0.369', '0.5845', '0.4866', '-0.1115', '-0.7935', '-0.6035', '0.297', '0.3936']",C26915,0004208,D014820,709.01,L80,,
mondo:0008662,autosomal dominant vitreoretinochoroidopathy,"['vitreoretinochoroidopathy, autosomal dominant, with nanophthalmos', 'vitreoretinochoroidopathy, autosomal dominant', 'VRCP', 'vitreoretinochoroidopathy with microcornea, glaucoma, and cataract', 'vitreoretinochoroidopathy', 'ADVIRC', 'VRCP autosomal dominant', 'vitreoretinochoroidopathy dominant', 'microcornea, Rod-cone dystrophy, cataract, and posterior staphyloma']",0111569,193220,3086,C3888099,"['-0.013336', '-0.8247', '-0.552', '-0.2424', '0.283', '0.2153', '-0.00596', '0.695', '-0.5884', '-0.1621', '-0.3142', '-0.553', '-0.174', '-0.1227', '-0.03647', '-0.0635', '0.04523', '-0.616', '0.557', '-0.785', '0.00784', '0.1405', '-0.05743', '0.01662', '0.02762', '0.1179', '0.0115', '0.2133', '0.429', '0.2524', '0.486', '-0.1365', '0.823', '0.5205', '-0.5005', '0.3413', '0.4824', '-0.3835', '0.786', '-0.776', '0.2856', '0.1128', '0.2478', '0.254', '-0.10266', '0.1884', '-0.12036', '0.1118', '-0.05515', '-0.1656', '0.547', '0.1964', '0.2659', '-0.3413', '0.2815', '-0.02702', '0.535', '0.0549', '-0.82', '0.09625', '-0.04904', '0.01234', '-0.01703', '0.01245', '-0.1693', '-0.013176', '0.5054', '0.3308', '-0.1493', '0.5063', '-0.413', '-0.05258', '-0.2112', '0.4421', '0.339', '-0.589', '0.171', '-0.11096', '-0.1106', '0.0275', '0.0735', '0.178', '-0.06604', '0.771', '0.0905', '-0.1144', '0.1696', '0.282', '0.1699', '0.4436', '0.00868', '0.2668', '0.0578', '0.3687', '0.928', '-0.3574', '0.919', '-0.0358', '-0.065', '0.1096']",,,C536352,,H35.5,,
mondo:0008663,snowflake vitreoretinal degeneration,"['snowflake vitreoretinal degeneration', 'SVD', 'vitreoretinal degeneration, snowflake type', 'snowflake degeneration in hereditary vitreoretinal degeneration']",0111570,193230,91496,C1860405,"['-0.4548', '-0.005028', '-0.005054', '0.0926', '0.3223', '-0.4487', '-0.2377', '0.10675', '-0.1711', '-0.3262', '-0.3306', '-0.2421', '-0.2429', '-0.2551', '0.2255', '-0.03015', '0.11414', '-0.002588', '-0.09863', '-0.4927', '-0.04898', '-0.1373', '0.02905', '0.1942', '0.1024', '0.1951', '-0.3582', '-0.03534', '-0.04855', '0.2147', '0.55', '-0.05194', '-0.10223', '-0.1365', '0.1044', '0.2123', '0.1654', '-0.2832', '0.08014', '-0.382', '0.2961', '-0.5684', '0.0804', '-0.1427', '-0.1619', '-0.1476', '0.1586', '0.00727', '0.04468', '-0.4014', '0.411', '-0.03632', '0.003119', '-0.01942', '-0.1143', '-0.4124', '0.7783', '0.06015', '-0.6577', '0.159', '0.1768', '-0.08575', '0.0619', '0.2053', '0.1505', '-0.10425', '0.3643', '0.509', '-0.285', '0.391', '-0.484', '-0.321', '-0.03784', '0.1451', '0.06177', '0.3125', '-0.2014', '0.2961', '-0.3796', '0.095', '0.2324', '0.1263', '-0.10626', '0.6377', '-0.1531', '-0.3162', '0.256', '0.525', '0.2064', '-0.001103', '-0.091', '0.369', '-0.02797', '-0.04803', '0.648', '-0.05762', '0.3257', '-0.4304', '-0.1418', '0.183']",,,C536677,,H35.5,,
mondo:0008665,ptosis-vocal cord paralysis syndrome,"['tucker syndrome', 'vocal cord paralysis and ptosis', 'ptosis vocal cord paralysis', 'congenital bilateral recurrent nerve paralysis and ptosis']",,193240,2997,C1860403,,,,C536923,,,,
mondo:0008666,volvulus of midgut,"['intestinal malrotation, familial', 'volvulus of midgut', 'congenital malrotation of intestine', 'intestinal malrotation']",,193250,,,,C98961,,C562456,,,,
mondo:0008667,von Hippel-Lindau disease,"['VHL syndrome', 'Von Hippel-Lindau syndrome, Modifiers of', 'Lindau disease', 'VHL', 'von Hippel-Lindau syndrome, modifier of', 'Von Hippel-Lindau syndrome (VHL)', 'familial cerebelloretinal angiomatosis', 'Hippel Lindau syndrome', 'cerebroretinal angiomatosis', 'Von Hippel Lindau disease', 'Von Hippel-Lindau syndrome', 'von Hippel-Lindau syndrome']",14175,193300,892,C0019562,"['0.1628', '0.6646', '-0.3264', '-0.3384', '-0.3113', '0.353', '0.3364', '0.835', '-0.5', '-0.1696', '-0.03293', '-0.1871', '-0.3162', '-0.0558', '0.1509', '-0.528', '-0.1008', '-0.398', '0.05457', '-0.06076', '-0.1106', '-0.6846', '0.2883', '-0.010925', '0.2546', '-0.5044', '0.1511', '-0.07904', '0.4175', '0.0555', '0.9663', '-0.1194', '0.8545', '-0.534', '-0.401', '0.2041', '-0.3184', '0.0885', '-0.0652', '0.1986', '-0.00822', '-0.2339', '1.107', '-0.579', '0.3726', '-0.397', '-0.515', '-0.0783', '0.4485', '-0.3647', '0.3164', '-0.02211', '-0.6553', '-0.3174', '-0.463', '0.03625', '0.798', '0.4075', '-0.1576', '0.521', '0.3474', '0.0506', '-0.1522', '0.06256', '-0.6455', '0.2262', '0.0507', '0.624', '0.04333', '0.6294', '0.0639', '-0.005096', '-0.432', '-0.411', '0.5415', '-0.624', '-0.205', '0.1423', '-0.3044', '0.01884', '-0.4683', '0.10504', '0.091', '0.0972', '-0.3862', '-0.6636', '0.7783', '-0.02785', '0.3767', '-0.157', '0.01701', '0.01773', '-0.0633', '-0.2128', '1.047', '-0.302', '0.352', '-0.0678', '0.4683', '0.2666']",C3105,,D006623,759.6,,10047716,
mondo:0008668,von Willebrand disease 1,"['von Willebrand disease type I', 'VON WILLEBRAND disease, type 1', 'Von Willebrand disease, type 1', 'VWD1', 'von Willebrand^s disease type 1', 'von willebrand^s disease 1', 'von Willebrand disease type 1', 'VWD, type 1', 'VWD type 1']",0060573,193400,166078,C1264039,"['-0.4065', '0.41', '-0.633', '0.1981', '-0.2625', '0.1425', '0.1265', '0.309', '-0.337', '-0.842', '0.1519', '0.6455', '0.4553', '0.934', '-0.174', '-0.8657', '0.3025', '0.10333', '-0.3318', '-0.637', '-0.343', '-0.619', '1.039', '-0.02786', '-0.3074', '-0.2954', '-0.3215', '-0.01901', '1.043', '0.2026', '0.755', '0.0968', '-0.0885', '0.2068', '0.0957', '-0.524', '-0.3357', '-0.02763', '0.1698', '-0.1552', '0.8584', '-0.0851', '0.3179', '-0.5947', '0.582', '-0.4827', '-0.9946', '0.0678', '0.11975', '-0.0924', '0.779', '-0.1056', '0.1236', '-0.06143', '-0.2554', '-0.3616', '-0.741', '0.8936', '-0.759', '-0.0665', '-0.4832', '0.2406', '0.538', '-0.902', '0.429', '-0.003193', '-0.002647', '-0.9487', '-0.7163', '0.3413', '-0.299', '0.24', '-0.4226', '-0.621', '0.586', '0.6978', '0.916', '0.2964', '0.487', '-0.10455', '-0.73', '-0.2827', '0.466', '-0.287', '-0.2683', '0.386', '-0.1077', '0.2303', '0.02931', '0.1503', '-0.549', '0.64', '-0.1156', '-0.02509', '1.2', '0.6426', '-0.013084', '-0.926', '-0.4392', '0.2375']",C131685,,D056725,,,,
mondo:0008669,"vulvovaginitis, allergic seminal","['vulvovaginitis, allergic seminal']",,193450,,C1860357,,,,C565993,,,,
mondo:0008670,Waardenburg syndrome type 1,"['Waardenburg^s syndrome type 1', 'Waardenburg syndrome with dystopia canthorum', 'Waardenburg syndrome, type 1', 'WS1', 'Waardenburg syndrome type I']",0110948,193500,894,C1847800,"['0.4272', '-0.03033', '-0.2234', '-0.0721', '0.7485', '-0.0855', '0.2021', '0.5483', '-0.5244', '-0.047', '-0.354', '-0.4946', '-0.04596', '0.1615', '-0.2448', '-0.4087', '0.3904', '-0.3284', '-0.547', '-0.4436', '-0.5103', '-0.443', '0.5557', '-0.4001', '-0.3313', '-0.3447', '-0.2751', '0.251', '0.4792', '-0.3616', '0.9014', '0.12274', '-0.36', '0.1538', '-0.1959', '0.2231', '0.010155', '-0.6587', '-0.2295', '-0.1732', '1.133', '-0.4417', '0.1818', '-0.3494', '-0.05563', '-0.6016', '0.5767', '0.3286', '-0.01892', '0.0803', '0.0231', '-0.608', '-0.0569', '-0.8438', '-0.4937', '-0.0779', '-0.1693', '0.0437', '-0.3599', '-0.2568', '-0.794', '-0.6523', '-0.02383', '-0.03488', '-0.3147', '-0.03455', '0.2382', '0.357', '-0.3867', '0.401', '-0.1692', '-0.1326', '-0.733', '0.07153', '0.2666', '-0.1987', '0.3364', '-0.901', '-0.2162', '-0.6724', '0.542', '-0.85', '-0.0731', '0.576', '-0.2106', '-0.3132', '0.0767', '0.543', '0.05893', '0.2305', '0.446', '1.062', '0.2866', '0.2776', '0.4526', '-0.6655', '0.2632', '-0.444', '-0.2454', '-0.2786']",C75008,,,,E70.3,,
mondo:0008671,Waardenburg syndrome type 2A,"['Waardenburg syndrome type IIA', 'WS2A', 'MITF Waardenburg syndrome type 2', 'Ws2', 'Waardenburg syndrome type 2 caused by mutation in MITF', 'Waardenburg syndrome without dystopia canthorum', 'Waardenburg syndrome, type 2A']",0110950,193510,,,,C75011,,C536464,,,,
mondo:0008672,Watson syndrome,"['pulmonic stenosis with cafe-Au-lait Spots', 'cafe-Au-lait Spots with pulmonic stenosis', 'Watson syndrome', 'WTSN']",,193520,3444,CN204429,"['-0.01152', '0.0693', '-0.004166', '-0.00891', '0.02985', '-0.0839', '-0.00483', '0.06366', '-0.0473', '-0.03038', '-0.01804', '-0.000702', '0.00568', '0.01567', '-0.009', '-0.02435', '-0.003906', '-0.01087', '-0.01426', '-0.0877', '-0.01564', '-0.02165', '0.04898', '-0.01119', '0.02127', '-0.004467', '-0.02573', '-0.02676', '0.02269', '-0.03638', '0.0667', '-0.0389', '0.0886', '0.02359', '0.02834', '-0.04028', '0.007065', '-0.0378', '0.0004485', '-0.0774', '0.0323', '-0.0784', '0.02144', '-0.0359', '0.01442', '-0.06064', '-0.02957', '0.04498', '0.01448', '-0.02022', '0.001816', '-0.02324', '0.0105', '0.02925', '-0.0309', '-0.0179', '0.06915', '-0.02501', '-0.06433', '-0.002348', '0.03516', '0.003872', '0.00505', '0.02296', '0.00814', '0.014755', '0.0692', '0.0366', '-0.0684', '0.0723', '-0.07135', '-0.00796', '0.00798', '-0.03778', '0.02208', '0.02985', '-0.013535', '0.006298', '-0.05933', '-0.0256', '0.02089', '0.0325', '-0.02243', '0.0472', '-0.03632', '-0.007797', '0.0499', '0.082', '0.05472', '0.00785', '0.01671', '0.064', '0.00425', '0.01542', '0.1442', '0.01965', '0.05005', '-0.11383', '-0.01796', '0.012184']",,,,709.8,,,
mondo:0008673,"acrofacial dysostosis, Weyers type","['curry-Hall syndrome', 'acrofacial dysostosis of Weyers', 'curry Hall syndrome', 'Weyers acrodental dysostosis', 'acrodental dysostosis of Weyers', 'Weyers acrofacial dysostosis', 'wad']",0111571,193530,952,C0457013,"['0.2339', '0.311', '0.609', '-0.4639', '0.548', '-0.4016', '0.0431', '0.4233', '-0.3088', '-0.4314', '0.1998', '-0.2764', '0.159', '0.1022', '-0.1048', '0.0628', '0.1713', '-0.3096', '-0.3958', '-0.7275', '-0.038', '-0.5044', '0.6426', '-0.2783', '0.0809', '0.4531', '-0.02693', '-0.134', '0.6245', '-0.05984', '0.2217', '0.2878', '-0.01765', '0.11084', '-0.1793', '-0.3342', '0.1733', '-0.3818', '-0.1284', '-0.1348', '0.07495', '-0.4436', '-0.095', '-0.1263', '-0.2164', '-0.391', '-0.1278', '0.514', '0.02318', '-0.1107', '0.3088', '0.0174', '0.02565', '-0.3179', '-0.3674', '-0.4504', '-0.1968', '-0.3818', '-0.3982', '0.1012', '-0.123', '0.1919', '-0.0761', '-0.562', '0.00977', '-0.263', '-0.02605', '0.03568', '-0.2201', '-0.01886', '-0.7603', '-0.523', '0.3157', '-0.31', '0.3345', '0.0829', '-0.4038', '0.0616', '-0.2654', '-0.624', '0.01828', '0.4487', '0.4211', '0.499', '-0.2883', '0.03247', '-0.1998', '-0.07153', '0.2166', '0.65', '-0.214', '0.3586', '0.3743', '0.683', '0.4058', '0.2476', '0.1664', '-0.8037', '0.0625', '0.2102']",,,C536695,520.8,,,
mondo:0008675,Freeman-Sheldon syndrome,"['FSS', 'craniocarpotarsal dystrophy', 'cranio-carpo-tarsal syndrome', 'distal arthrogryposis type 2A', 'whistling face syndrome', 'Craniocarpotarsal dysplasia', 'craniocarpotarsal dysplasia', 'windmill-vane-hand syndrome', 'arthrogryposis, distal, type 2A (Freeman-Sheldon)', 'Freeman-Sheldon syndrome', 'Craniocarpotarsal dystrophy', 'DA2A', 'arthrogryposis, distal, type 2A', 'whistling face-windmill vane hand syndrome', 'whistling-face syndrome', 'arthrogryposis distal type 2A', 'Freeman Sheldon syndrome']",0111605,193700,2053,C0265224,"['-0.3423', '-0.4468', '-0.2563', '-0.4546', '0.3765', '-0.753', '0.516', '1.26', '-1.033', '-0.814', '0.2094', '-0.01772', '-0.1635', '0.2072', '-0.1421', '0.6455', '0.4587', '-0.1722', '0.14', '-0.6895', '0.0798', '-0.5664', '0.04868', '0.1691', '-0.2261', '0.13', '-0.9204', '0.1946', '0.462', '-0.449', '0.3867', '-0.0549', '0.0228', '0.3806', '0.1395', '-0.4495', '0.1715', '-0.2455', '0.3555', '0.1449', '-0.04013', '-0.1628', '0.06', '-0.4302', '0.236', '0.03537', '0.1993', '0.5923', '-0.1109', '0.3628', '-1.006', '-0.0636', '0.005898', '-0.2644', '-0.4958', '-0.0739', '-0.2844', '-0.625', '0.3298', '-0.57', '0.3228', '0.02306', '-0.6973', '0.1251', '0.2537', '0.26', '0.3652', '-0.1373', '0.1931', '0.803', '0.0167', '-0.04105', '0.09875', '-0.1006', '-0.171', '0.1938', '0.2189', '-0.512', '-0.2727', '0.577', '0.06445', '-0.5864', '-0.04123', '1.105', '-0.3364', '-0.1321', '-0.172', '-0.142', '0.286', '-0.257', '0.04932', '-0.002682', '0.2825', '0.5796', '0.327', '0.3142', '0.6636', '-0.4136', '0.522', '0.01761']",C98931,,C535483,,,,
mondo:0008676,white sponge nevus 1,"['White sponge Nevus of Cannon', 'WSN1', 'leukokeratosis, hereditary mucosal', 'KRT4 hereditary mucosal leukokeratosis', 'hereditary mucosal leukokeratosis caused by mutation in KRT4', 'white sponge nevus 1', 'White sponge Nevus type 1', 'WHITE sponge NEVUS 1']",0081287,193900,,C4011926,,,,,,,,
mondo:0008678,Williams syndrome,"['Williams-Beuren syndrome (WBS)', 'Williams syndrome', 'monosomy 7q11.23', 'Williams-Beuren syndrome', 'chromosome 7Q11.23 deletion syndrome, 1.5- to 1.8-Mb', 'WBS', 'Fanconi Schlesinger syndrome', 'WMS', 'deletion 7q11.23']",1928,194050,904,C0175702,"['0.2032', '-0.0207', '0.545', '-0.2438', '-0.05185', '-0.2162', '0.6396', '1.507', '-0.7686', '0.3018', '-0.1215', '-0.0285', '0.3967', '0.1554', '0.003271', '-0.005573', '-0.001684', '0.1987', '-0.3513', '-0.02483', '-0.004967', '0.0837', '-0.1046', '-0.135', '-0.3', '-0.1829', '0.09576', '-0.1855', '0.346', '-0.05597', '0.2656', '-0.1987', '0.5835', '-0.3901', '-0.3105', '0.2249', '-0.284', '-0.235', '0.1279', '-0.5205', '0.2395', '0.08093', '0.296', '0.1831', '0.6323', '-0.2095', '0.366', '0.527', '-0.2074', '0.114', '-0.5605', '0.7886', '-0.4675', '0.1276', '-0.0977', '0.02484', '0.1632', '0.03687', '0.2878', '0.1656', '0.69', '0.822', '-0.5103', '-0.07025', '0.2668', '0.07275', '0.03662', '0.07367', '-0.129', '0.2379', '-0.04462', '-0.1892', '-0.454', '-0.1678', '-0.0135', '-0.2025', '0.3218', '-0.03708', '-0.691', '0.06714', '0.2668', '-0.693', '-0.1556', '0.419', '-0.2197', '0.4407', '0.03041', '0.1891', '0.4211', '-0.02242', '0.2313', '0.4863', '-0.4468', '-0.1688', '0.8857', '-0.298', '0.4824', '-0.3777', '-0.0649', '0.4287']",C85232,,D018980,759.89,,10049644,
mondo:0008679,Wilms tumor 1,"['Wilms^ tumour', 'Wilms tumor, somatic', 'WT1', 'nephroblastoma', 'Wilms tumour type 1', 'Wilms^ tumor', 'renal Wilms tumour', 'renal Wilms tumor', 'Wilms tumor, autosomal dominant, somatic mutation', 'Wilms tumor 1', 'Wilms tumor, type 1, autosomal dominant, somatic mutation', 'Wilms tumor type 1']",,194070,,CN033288,,C6180,,,,,,
mondo:0008680,Wilms tumor 2,"['FWT2', 'Wilms tumor 2, autosomal dominant, somatic mutation', 'familial Wilms tumor 2', 'familial Wilms tumour 2', 'WT2', 'Wilms tumor type 2', 'Wilms tumor 2', 'Wilms tumour 2, autosomal dominant, somatic mutation', 'Wilms tumour type 2']",,605982,,,,,,C536853,,,,
mondo:0008681,WAGR syndrome,"['Wilms tumor, aniridia, genitourinary anomalies and developmental delay syndrome', 'chromosome 11P13 deletion syndrome', 'Wilms tumor-aniridia-genitourinary anomalies-intellectual disability syndrome', 'Wilms tumor-aniridia-gonadoblastoma-intellectual disability syndrome', 'AGR triad', 'partial monosomy 11p', 'Del(11)(p13)', 'WAGR', 'deletion 11p13', 'chromosome 11p deletion', 'Wilms tumor, aniridia, genitourinary anomalies and mental retardation syndrome, autosomal dominant, somatic mutation', 'chromosome 11p deletion syndrome', 'Wilms tumor, aniridia, genitourinary anomalies, mental retardation syndrome', 'WAGR 11p13 deletion syndrome', '11p deletion syndrome', 'WAGR Complex', 'monosomy 11p', 'WAGR syndrome', 'Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome', '11p deletion', 'chromosome 11p13 deletion syndrome', 'Wilms tumor, aniridia, genitourinary anomalies, intellectual disability syndrome', 'Wilms tumor-aniridia-gonadoblastoma-mental retardation syndrome', '11p partial monosomy syndrome', 'Wilms tumor, aniridia, genitourinary anomalies, and mental retardation syndrome', 'monosomy 11p13', 'deletion 11p', 'Wilms tumor, aniridia, genitourinary anomalies, and intellectual disability syndrome', '11p monosomy']",14515,194072,893,C2931803,,C3718,,D017624,,,,
mondo:0008682,Denys-Drash syndrome,"['Denys-Drash syndrome, autosomal dominant, somatic mutation', 'Drash syndrome', 'pseudohermaphroditism, nephron disorder and Wilms^ tumour', 'nephropathy, Wilms tumor, and genital anomalies', 'Wilms tumor and pseudohermaphroditism', 'Denys Drash syndrome', 'Denys-Drash syndrome', 'DDS', 'nephrotic syndrome type 4', 'Wilms tumor and pseudo- or true hermaphroditism', 'Wilms tumour and pseudo- or true hermaphroditism', 'nephropathy associated with male pseudohermaphroditism and Wilms^ tumor', 'Wilms tumour and pseudohermaphroditism', 'nephropathy associated with male pseudohermaphroditism and Wilms^ tumour', 'pseudohermaphroditism, nephron disorder and Wilms^ tumor']",3764,194080,220,C3151568,"['0.669', '-0.327', '-0.545', '-0.1381', '-0.1901', '-0.6807', '0.6245', '0.7466', '-0.4812', '-0.5845', '0.2231', '-0.1981', '-0.1555', '0.509', '0.10016', '-0.6147', '0.1265', '-0.1752', '0.2378', '-0.4602', '0.1183', '0.45', '0.5337', '-0.734', '0.607', '-0.3953', '-0.1433', '0.3962', '-0.05453', '-0.9014', '0.9546', '0.086', '0.8164', '-0.01382', '0.011765', '-1.04', '-0.3413', '0.2554', '-0.6187', '0.07056', '-0.1506', '0.2993', '0.1902', '-0.6934', '0.2368', '0.02913', '-0.4272', '-0.6104', '-0.1167', '0.539', '-0.2698', '0.326', '0.1059', '-0.4062', '-0.3074', '0.03943', '0.2264', '-0.2456', '-0.827', '0.6133', '0.5884', '0.2842', '0.1829', '0.554', '0.0277', '-0.1562', '0.6367', '0.4414', '-0.1565', '0.0863', '0.0918', '0.2957', '-0.3135', '0.4414', '0.2573', '-0.2262', '0.3093', '0.2179', '-0.7056', '0.06256', '0.0824', '0.838', '0.2932', '0.57', '-0.5366', '-0.301', '0.2063', '-0.1417', '-0.4622', '0.1517', '0.2932', '0.655', '-0.3923', '0.08325', '0.388', '-0.3542', '0.533', '-0.5674', '-0.5654', '0.2225']",C84668,,D030321,189.0,,10070179,
mondo:0008683,Wilms tumor 3,"['Wilms tumor 3', 'WT3', 'Wilms tumor, type 3']",,194090,,C1860265,,,,C565991,,,,
mondo:0008684,Wolf-Hirschhorn syndrome,"['Wolf-Hirschhorn syndrome', 'Wolf syndrome', 'distal monosomy 4p', 'Pitt-Rogers-Danks syndrome', 'telomeric deletion 4p', 'chromosome 4P16.3 deletion syndrome', 'chromosome 4p syndrome', 'distal deletion 4p', 'WHS', 'Wolf-Hirschhorn syndrome, Isolated cases', '4p syndrome', '4p deletion syndrome', '4p- syndrome', 'chromosome 4p16.3 deletion syndrome', 'Pitt syndrome', 'Wittwer syndrome', 'microcephaly, IUGR, hypertelorism, ptosis, iris coloboma, hooked nose, external ear dysplasia, psychomotor retardation']",0050460,194190,280,CN207113,,C35528,,D054877,,Q93.3,10050361,
mondo:0008685,Wolff-Parkinson-White syndrome,"['anomalous A-V excitation', 'WPW', 'Wolff-Parkinson-White pattern (finding)', 'ventricular familial preexcitation syndrome', 'Wolff-Parkinson-White pattern', 'preexcitation syndrome', 'Wolff-Parkinson-White syndrome', 'anomalous atrioventricular excitation', 'Wpw syndrome', 'Wolff-Parkinson-white syndrome (disease)', 'accessory atrioventricular pathways']",384,194200,907,,"['-0.1393', '0.3127', '0.1855', '0.204', '-0.4563', '-0.338', '0.4429', '0.676', '-0.04315', '-0.2268', '0.4624', '-0.09106', '-0.1116', '0.26', '-0.1749', '0.2252', '-1.017', '0.03964', '-0.6694', '-0.392', '0.508', '0.5015', '0.806', '-0.2686', '0.3489', '-0.6675', '0.1277', '-0.2642', '0.4424', '0.6733', '0.2031', '0.251', '0.1901', '-0.06158', '-0.5396', '-0.2024', '0.3894', '0.4697', '0.2404', '-0.2294', '0.2167', '0.5005', '-0.2162', '0.0828', '0.3237', '0.1127', '-0.6216', '0.3247', '0.398', '0.3372', '-0.168', '0.0956', '-0.746', '-0.2192', '-0.3887', '-0.1923', '-0.05444', '0.3738', '-0.3833', '-0.023', '-0.486', '0.292', '0.0558', '-0.4104', '-0.5894', '-0.1421', '0.6035', '0.8926', '-0.5513', '0.581', '-0.598', '0.814', '0.3862', '-0.6597', '-0.387', '0.835', '-0.1285', '0.2766', '-0.7026', '-0.11615', '0.08655', '-0.2183', '0.253', '-0.1549', '0.4', '-0.3364', '0.6035', '-0.1522', '0.5103', '0.1531', '0.1562', '-0.0492', '0.08875', '-0.00913', '0.6807', '0.4475', '-0.1302', '-1.15', '-0.655', '0.635']",C35132,1001450,D014927,426.7,,,0001716
mondo:0008686,isolated familial wooly hair disorder,"['wooly hair syndrome', 'familial wooly hair (autosomal recessive)', 'woolly hair syndrome', 'hereditary woolly hair syndrome', 'familial wooly hair syndrome', 'wooly hair', 'woolly hair', 'familial woolly hair syndrome', 'ADWH', 'hereditary woolly hair (autosomal dominant)', 'hereditary wooly hair (autosomal dominant)', 'woolly hair, autosomal dominant', 'familial woolly hair (autosomal recessive)', 'hereditary wooly hair syndrome', 'wooly hair, autosomal dominant']",0111572,,170,CN200245,"['-0.3835', '0.138', '-0.2954', '-0.02414', '0.7207', '-0.285', '0.4773', '0.5366', '0.1346', '-0.6265', '0.1605', '-0.2244', '-0.07983', '0.617', '-0.0729', '0.2136', '0.1705', '-0.389', '0.02864', '-1.099', '0.256', '0.0845', '0.875', '-0.319', '0.2052', '0.0849', '0.1821', '0.4204', '0.2957', '0.3535', '0.869', '-0.03925', '0.01874', '0.04318', '-0.361', '0.4998', '-0.297', '-0.153', '0.3591', '0.1926', '0.4966', '0.03088', '0.0483', '-0.1437', '0.2415', '-0.03925', '-0.2467', '-0.11884', '-0.055', '-0.4446', '-0.007393', '0.1716', '0.2035', '0.1823', '-0.3638', '-0.0005627', '0.4263', '-0.1986', '-0.5557', '-0.4956', '0.2299', '0.128', '-0.1438', '-0.241', '0.1031', '0.545', '0.4805', '-0.11926', '-0.1501', '0.4106', '-0.558', '-0.076', '0.441', '0.02292', '-0.01482', '-0.2625', '0.168', '-0.1865', '-0.1368', '-0.6416', '0.2668', '0.2195', '0.05597', '-0.10175', '0.5137', '-0.3215', '0.315', '0.088', '0.2783', '0.679', '0.6357', '0.07306', '0.12054', '0.675', '0.0617', '-0.1688', '0.2842', '-0.2429', '0.0362', '0.1388']",,,C536745,,,10048017,0002224
mondo:0008687,Woronets trait,['Woronets trait'],,194320,,,,,,,,,,
mondo:0008688,WT limb-blood syndrome,"['WT limb-blood syndrome', 'radial-ulnar hypoplasia with bone marrow failure and/or leukaemia', 'WTsyndrome', 'radial-ulnar hypoplasia with bone marrow failure and/or leukemia', 'WT limb blood syndrome']",,194350,3466,C1327917,,,,C536751,,,,
mondo:0008689,dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema,"['pseudohyperkalemia, familial, 1, due to Red cell leak', 'DEHYDRATED hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal oedema', 'dehydrated hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema', 'DEHYDRATED hereditary stomatocytosis 1 with or without pseudohyperkalemia and/OR perinatal oedema', 'DEHYDRATED hereditary stomatocytosis 1 with or without pseudohyperkalemia and/OR perinatal edema', 'DHS', 'Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/Or perinatal edema', 'Dehydrated hereditary stomatocytosis pseudohyperkalemia and perinatal edema', 'Desiccytosis, hereditary', 'dehydrated hereditary stomatocytosis', 'pseudohyperkalemia Edinburgh', 'xerocytosis, hereditary', 'Dehydrated hereditary stomatocytosis pseudohyperkalemia and perinatal oedema', 'Dehydrated hereditary stomatocytosis 1 with or without pseudohyperkalemia and/Or perinatal oedema', 'DHS1', 'DEHYDRATED hereditary stomatocytosis with or without pseudohyperkalemia and/or perinatal edema']",0111576,194380,,,,,,,,,,
mondo:0008690,"xeroderma pigmentosum, autosomal dominant, mild","['xeroderma pigmentosum, autosomal dominant, mild']",,194400,,C1860231,,,,C565989,,,,
mondo:0008691,"zinc, elevated plasma","['albumin binding of zinc, elevated', 'hyperzincemia and hypercalprotectinemia', 'zinc, elevated plasma', 'hyperzincemia, familial Dysalbuminemic']",,194470,,,,,,,,,,
mondo:0008692,abetalipoproteinemia,"['congenital betalipoprotein deficiency syndrome', 'ABL', 'microsomal triglyceride transfer protein deficiency disease', 'Betalipoprotein deficiency disease', 'homozygous familial hypobetalipoproteinemia', 'abetalipoproteinemia neuropathy', 'apolipoprotein B deficiency', 'abetalipoproteinemia', 'familial hypobetalipoproteinemia', 'MTP deficiency', 'Bassen-Kornzweig syndrome', 'acanthocytosis', 'Bassen-Kornzweig disease', 'microsomal triglyceride transfer Protein deficiency', 'Bassen Kornzweig syndrome']",1386,200100,14,C0000744,"['-0.11676', '0.4946', '0.06116', '-0.2032', '0.1697', '-0.126', '-0.37', '0.7153', '-0.391', '-0.1768', '-0.273', '0.1011', '0.322', '-0.1962', '-0.0211', '-0.6353', '0.4006', '0.1838', '-0.1484', '-0.745', '0.1426', '-0.5337', '0.3757', '0.4785', '-0.02043', '0.4768', '0.09546', '-0.2021', '-0.3389', '-0.705', '1.01', '0.2524', '0.518', '0.3203', '-0.7534', '0.3474', '-0.4487', '0.0512', '-0.391', '-0.358', '-0.4631', '0.11365', '0.2686', '0.02884', '-0.2375', '-0.391', '0.2488', '0.1823', '-0.5186', '-0.1945', '-0.2244', '0.389', '-0.1688', '-0.2725', '-0.1098', '-0.03638', '0.3967', '-0.296', '-0.577', '0.3657', '0.2625', '0.5444', '0.1909', '-0.452', '-0.1572', '0.03044', '-0.03238', '0.2247', '-0.4766', '-0.3147', '-0.722', '-0.00894', '0.1672', '0.1385', '0.4978', '-0.02498', '0.001306', '-0.07434', '-0.0694', '0.3928', '0.068', '-0.139', '-0.9805', '-0.02766', '0.1556', '-0.0413', '0.0831', '-0.3113', '0.4834', '0.0951', '0.1577', '-0.0665', '-0.2744', '-0.2084', '0.2412', '0.68', '0.617', '-0.903', '-0.3513', '0.0424']",C84525,,D000012,,,,
mondo:0008693,ablepharon macrostomia syndrome,"['congenital ablepharon, absent eyelashes/eyebrows, macrostomia, auricular, nasal, genital and other systemic anomalies', 'AMS', 'ablepharon-macrostomia syndrome']",0060550,200110,920,C1860224,"['-0.1865', '-0.2861', '0.09595', '-0.6973', '0.497', '-0.811', '0.1877', '0.3984', '-0.3665', '-0.5244', '0.2983', '-0.1493', '-0.4568', '0.174', '-0.352', '0.2593', '0.4683', '-0.07684', '-0.3228', '-0.6953', '-0.1517', '-0.3933', '-0.05237', '-0.7324', '0.3655', '0.05026', '-0.6826', '0.503', '0.593', '-1.033', '0.601', '-0.2676', '0.03864', '0.6367', '-0.1226', '-0.0986', '-0.4265', '0.1033', '-0.3496', '-0.1948', '0.4802', '-0.1838', '-0.0828', '-0.6875', '0.8174', '-0.52', '-0.005035', '0.734', '-0.486', '-0.4358', '-0.3774', '0.4504', '-0.2383', '0.1826', '-0.514', '-0.09534', '-0.01424', '-0.3953', '-0.6445', '-0.1335', '-0.08563', '-0.03998', '-0.2566', '0.175', '0.2024', '0.02179', '-0.03516', '-0.08356', '-0.3452', '0.492', '-0.752', '0.2413', '0.10004', '0.3264', '-0.1271', '0.0601', '0.627', '0.007145', '-0.3767', '-0.4392', '-0.1305', '-0.2302', '0.1536', '0.0945', '0.586', '-0.2097', '-0.1158', '0.4956', '0.03964', '0.1501', '0.3425', '0.9897', '0.3264', '0.1581', '0.6343', '0.0775', '0.1487', '-0.5317', '0.3438', '0.2744']",,,C535557,,,,
mondo:0008694,pseudoprogeria syndrome,"['mental retardation, absence of eyebrows and eyelashes, progressive spastic quadriplegia, microcephaly, glaucoma, and small, beaked nose', 'intellectual disability, absence of eyebrows and eyelashes, progressive spastic quadriplegia, microcephaly, glaucoma, and small, beaked nose', 'absent eyebrows and eyelashes-intellectual disability syndrome', 'absent eyebrows and eyelashes with mental retardation', 'eyebrows and eyelashes absence-intellectual disability syndrome', 'Hal-Berg-Rudolph syndrome', 'pseudoprogeria syndrome', 'absent eyebrows and eyelashes with intellectual disability']",,200130,2985,C0796125,,,,C563111,,,,
mondo:0008695,chorea-acanthocytosis,"['CHOREOACANTHOCYTOSIS', 'Chac', 'acanthocytosis with neurologic disorder', 'choreoacanthocytosis', 'neuroacanthocytosis', 'chorea-acanthocytosis', 'Levine-Critchley syndrome', 'choreo-acanthocytosis', 'chorea acanthocytosis', 'choreaacanthocytosis']",0050766,200150,2388,,"['-0.0659', '0.3032', '-0.2396', '-0.1095', '-0.207', '-0.796', '-0.0206', '0.589', '-0.3206', '-0.254', '0.3367', '-0.06', '-0.2888', '-0.0681', '0.4011', '0.305', '0.05838', '-0.504', '-0.2185', '-0.767', '0.02103', '-0.04153', '0.555', '0.09467', '-0.07007', '0.09503', '-0.378', '-0.2362', '-0.2491', '-0.33', '0.5063', '-0.1288', '0.2241', '-0.2334', '-0.02141', '0.00998', '0.3137', '-0.3865', '-0.2305', '0.1754', '0.3577', '-0.6196', '0.2028', '-0.0986', '0.8877', '-0.2988', '-0.1871', '0.11224', '0.0917', '0.53', '-0.01418', '0.6797', '-0.317', '-0.4163', '0.595', '0.1074', '1.013', '-0.2732', '-0.0914', '0.136', '-0.4092', '-0.1492', '0.3894', '-0.344', '-0.6465', '0.2054', '0.11505', '0.2417', '0.1791', '0.4912', '-0.01743', '-0.3464', '0.3638', '0.589', '0.29', '0.2253', '0.2087', '0.2191', '-0.2512', '-0.6123', '0.6333', '-1.129', '-0.0675', '0.5396', '0.273', '-0.0806', '0.1146', '0.0808', '0.5703', '-0.0948', '0.2491', '-0.01114', '0.1647', '0.303', '0.3257', '0.5176', '-0.01321', '0.127', '0.05762', '0.08545']",,,,333.0,,,
mondo:0008696,acanthosis nigricans-insulin resistance-muscle cramps-acral enlargement syndrome,"['acanthosis nigricans with muscle cramps and acral enlargement', 'familial insulin resistance with acanthosis nigricans, acral hypertrophy and muscle cramps', 'acanthosis nigricans muscle cramps acral enlargement']",,200170,90301,C1860215,,,,C536000,,,,
mondo:0008698,achalasia,"['esophageal achalasia', 'lack of reflex relaxation of lower oesophageal sphincter', 'achalasia', 'hypertensive lower esophageal sphincter', 'cardiospasm', 'achalasia of esophagus', 'achalasia of oesophagus', 'achalasia (disease)', 'achalasia of cardia']",9164,,,C2939435,,,,,530.0,,,0002571
mondo:0008699,achalasia microcephaly syndrome,"['achalasia microcephaly', 'achalasia-microcephaly syndrome']",0050796,200450,929,C1860212,,,,C536010,,,,
mondo:0008700,acheiropody,"['acheiropodia', 'acheiropody, Brazilian type', 'acheiropody', 'ACHP', 'horn-Kolb syndrome']",0050603,200500,931,,"['-0.4595', '0.1348', '-0.003424', '-0.589', '0.4446', '-0.61', '-0.1425', '0.4236', '-0.3035', '-0.644', '-0.189', '-0.1741', '-0.09894', '0.12335', '-0.2656', '0.115', '0.3955', '0.3167', '-0.1868', '-0.3655', '-0.1399', '-0.1539', '0.2222', '-0.2964', '0.3367', '0.3142', '-0.01573', '0.2542', '0.4055', '-0.0696', '0.1256', '-0.4504', '-0.0724', '0.593', '0.05637', '-0.1815', '0.1582', '-0.3838', '0.1454', '-0.344', '-0.702', '-0.621', '0.2216', '-0.3225', '0.2583', '-0.315', '-0.306', '0.3687', '-0.014595', '-0.02138', '0.2035', '0.1504', '0.1937', '-0.1019', '-0.556', '-0.6196', '0.43', '0.02312', '-0.597', '-0.3777', '0.3894', '0.01299', '-0.1317', '-0.0933', '-0.11646', '0.00829', '0.0369', '0.4663', '-0.1076', '0.4229', '-0.01773', '-0.314', '0.0713', '-0.1206', '0.3984', '0.1454', '-0.193', '0.4822', '-0.3677', '-0.3545', '-0.616', '0.1786', '0.8867', '0.545', '-0.0823', '0.1721', '-0.5195', '0.4807', '-0.2866', '-0.3162', '-0.0773', '0.0503', '-0.2908', '-0.01182', '0.751', '-0.23', '0.901', '-0.5444', '0.1503', '0.0839']",,,C536014,,,,
mondo:0008701,achondrogenesis type IA,"['Houston-Harris achondrogenesis', 'achondrogenesis Houston-Harris type', 'ACG1A', 'achondrogenesis, Houston-Harris type', 'achondrogenesis type 1A', 'achondrogenesis, type 1A', 'achondrogenesis, type IA']",0080054,200600,93299,,"['-0.5254', '0.1166', '0.1292', '-0.1572', '0.3975', '-0.2439', '-0.2241', '0.298', '-0.471', '-0.002237', '-0.1282', '0.134', '0.3318', '0.086', '-0.421', '0.03091', '0.2808', '0.187', '-0.1935', '-0.719', '0.0864', '0.1667', '0.873', '-0.02852', '-0.1338', '-0.04755', '-0.111', '-0.32', '0.4407', '-0.2246', '-0.00892', '-0.0794', '0.2262', '0.315', '0.0314', '-0.1644', '-0.1368', '0.0627', '-0.1986', '-0.6387', '-0.01643', '-0.621', '-0.0202', '-0.1572', '-0.078', '-0.3125', '-0.011986', '0.8037', '0.657', '-0.10126', '0.1935', '-0.2408', '-0.02306', '0.12036', '-0.5186', '-0.8506', '-0.5073', '0.11804', '0.05978', '-0.09265', '0.4126', '-0.0353', '-0.2732', '0.1261', '-0.27', '0.02722', '0.02', '0.2944', '-0.3752', '0.4717', '0.0703', '-0.143', '0.4763', '-0.192', '-0.0828', '0.2527', '-0.4563', '0.3606', '-0.378', '-0.694', '-0.02759', '-0.2311', '-0.267', '0.1312', '-0.1912', '0.2908', '0.1447', '0.2441', '0.4502', '-0.05298', '-0.151', '0.0997', '0.1863', '0.3171', '0.419', '0.358', '0.2998', '-0.3606', '0.2477', '0.1343']",,,C536015,756.9,,,
mondo:0008702,achondrogenesis type II,"['achondrogenesis, type IB, formerly', 'hypochondrogenesis', 'ACG2', 'achondrogenesis, Langer-Saldino type', 'achondrogenesis, type IB', 'chondrogenesis imperfecta', 'achondrogenesis, type II or hypochondrogenesis', 'achondrogenesis, type II', 'achondrogenesis type 2', 'achondrogenesis, type 2']",0080056,200610,93297,,"['0.009796', '0.0739', '0.1979', '-0.3413', '0.3965', '-0.503', '-0.02472', '0.2356', '-0.9653', '-0.563', '0.06647', '0.003925', '0.1935', '-0.2163', '-0.3728', '0.02528', '0.05222', '-0.05676', '-0.1342', '-0.2788', '-0.00806', '-0.0497', '0.857', '-0.1818', '0.29', '0.0853', '-0.05334', '-0.06305', '0.3647', '-0.294', '0.2429', '-0.1425', '0.4014', '0.245', '0.1903', '-0.0576', '-0.3975', '0.1489', '0.1171', '-0.5425', '-0.1343', '-0.3877', '-0.3816', '0.001103', '-0.6543', '-0.4033', '0.1754', '0.6978', '0.848', '0.00872', '0.08545', '-0.279', '-0.2007', '0.3047', '-0.2249', '-0.869', '-0.3618', '0.2052', '0.296', '0.04974', '0.1932', '0.2573', '-0.3203', '0.1628', '-0.2817', '-0.0726', '0.1317', '-0.0908', '-0.5317', '0.352', '0.06287', '0.2428', '0.428', '0.2815', '-0.2778', '0.3586', '-0.1594', '0.3472', '-0.4739', '-0.2314', '-0.501', '0.0068', '-0.358', '0.002352', '-0.628', '-0.0719', '0.085', '0.2776', '0.38', '-0.1982', '-0.3174', '0.1203', '0.487', '0.1824', '0.6772', '0.3054', '0.00809', '-0.2255', '0.4827', '0.1366']",,,C536017,,,,
mondo:0008703,acromesomelic dysplasia 2A,"['hypochondrogenesis', 'Langer-Saldino achondrogenesis', 'GREBE chondrodysplasia', 'achondrogenesis, Brazilian', 'acromesomelic dysplasia 2A', 'Grebe chondrodysplasia', 'achondrogenesis, type II, formerly', 'acromesomelic dysplasia, Grebe type', 'Grebe syndrome', 'achondrogenesis type II (formerly)', 'chondrodysplasia, Grebe type', 'Brazilian achondrogenesis', 'achondrogenesis, type II', 'AMDG', 'type II achondrogenesis', 'Grebe dysplasia']",0080052,200700,2098,C0265260,"['-0.181', '0.2798', '0.355', '-0.2212', '0.5938', '-0.52', '-0.3875', '0.495', '-0.637', '-0.669', '-0.04504', '0.1415', '-0.3196', '-0.0625', '-0.291', '0.1373', '0.545', '-0.05975', '-0.4785', '-0.771', '-0.187', '0.11646', '1.01', '0.1216', '0.2588', '0.07965', '0.12103', '0.0899', '0.4172', '0.1709', '-0.06128', '-0.2346', '-0.149', '0.387', '0.3022', '-0.3374', '-0.2014', '-0.2644', '0.1423', '-0.2483', '-0.3738', '-0.4668', '-0.09503', '0.2006', '-0.4465', '-0.4702', '-0.27', '0.522', '0.947', '-0.01958', '0.4648', '-0.433', '-0.04254', '-0.1185', '-0.3083', '-0.8633', '-0.2827', '0.0465', '0.08765', '0.129', '0.1929', '0.4553', '-0.2157', '0.3765', '-0.1742', '-0.3545', '0.11365', '0.3762', '-0.5166', '0.3184', '-0.285', '0.158', '0.322', '-0.2279', '-0.2128', '0.2961', '-0.2878', '0.5034', '-0.489', '-0.3914', '-0.4915', '0.1109', '-0.0528', '-0.1729', '-0.5044', '0.0552', '-0.182', '0.3052', '0.1787', '0.1348', '-0.3984', '0.3037', '0.3262', '0.1564', '0.3713', '0.5874', '0.5796', '-0.679', '0.6025', '0.2133']",C3816,,,,,,
mondo:0008704,short-limb skeletal dysplasia with severe combined immunodeficiency,"['achondroplasia, so-called, and severe combined immunodeficiency', 'short limb skeletal dysplasia with SCID', 'achondroplasia-SCID syndrome', 'achondroplasia-severe combined immunodeficiency syndrome', 'short-limb skeletal dysplasia with severe combined immunodeficiency', 'achondroplasia and Swiss type agammaglobulinemia', 'achondroplasia and severe combined immunodeficiency', 'SLSD with SCID', 'achondroplasia and Swiss-type agammaglobulinemia', 'Slsd with SCID', 'achondroplasia-Swiss type agammaglobulinemia syndrome', 'immunodeficiency-short limb dwarfism syndrome', 'achondroplasia so-called and severe combined immunodeficiency', 'agammaglobulinemia and achondroplasia']",,200900,935,C1860168,,,,C565984,,,,
mondo:0008705,lysosomal acid phosphatase deficiency,"['acid phosphatase deficiency', 'lysosomal acid phosphatase deficiency']",,200950,35121,C0268410,,,,C562645,277.6,E83.3,,
mondo:0008706,Ackerman syndrome,"['glaucoma, juvenile, with unusual upper lip and dental roots', 'molar roots, pyramidal, with juvenile glaucoma and unusual upper lip', 'juvenile glaucoma with unusual upper lip and dental roots', 'pyramidal molar-glaucoma-upper abnormal lip syndrome', 'Ackerman syndrome', 'Ackerman fused molar rooth syndrome', 'pyramidal molars, glaucoma, abnormal upper lip']",,200970,2561,C1860167,,,,C538170,,,,
mondo:0008707,acro-renal-mandibular syndrome,"['acrorenal-uterine-mandibular syndrome', 'split hand/split foot-mandibular hypoplasia syndrome', 'acrorenal-mandibular syndrome', 'split hand split foot mandibular hypoplasia', 'acrorenal mandibular syndrome', 'acro-renal-uterine-mandibular syndrome', 'split-hand and split-foot with mandibular hypoplasia']",,200980,958,C1860166,,,,C535665,,,,
mondo:0008708,acrocallosal syndrome,"['ACLS', 'Schinzel syndrome 1', 'ACS', 'absence of corpus callosum with unusual facial appearance, mental deficiency, duplication of the halluces and polydactyly', 'hallux Duplication, postaxial polydactyly, and absence of corpus callosum', 'acrocallosal syndrome, Schinzel type', 'Schinzel acrocallosal syndrome', 'Joubert syndrome 12', 'Joubert syndrome 12/15, digenic', 'acrocallosal syndrome']",9250,200990,36,C0796147,"['-0.06433', '0.02931', '0.5054', '-0.605', '-0.02037', '-0.3855', '-0.1322', '1.046', '-0.777', '-0.897', '-0.3657', '-0.869', '0.2424', '0.2505', '-0.3508', '-0.3147', '0.3877', '-0.587', '-0.1903', '-0.6226', '0.02763', '0.14', '0.321', '-0.4817', '0.2147', '0.02533', '-0.1307', '0.2712', '0.742', '-0.3416', '0.4382', '-0.544', '0.1526', '-0.4683', '0.03021', '0.2245', '-0.2737', '-0.2258', '-0.2108', '-0.05072', '0.1765', '-0.2668', '0.10126', '-0.3367', '0.713', '-0.3633', '0.1102', '0.5522', '-0.5396', '-0.2156', '0.2458', '-0.04712', '-0.863', '-0.218', '-0.8726', '-0.628', '-0.08673', '-0.1233', '-0.2413', '0.739', '0.057', '-0.3823', '-0.2996', '0.01062', '-0.3413', '-0.1648', '0.1926', '0.0988', '-0.6143', '0.179', '-0.1482', '0.1895', '0.116', '-0.02571', '-0.2644', '0.7715', '0.511', '-0.1199', '-0.325', '0.0691', '0.0748', '0.1017', '0.3943', '0.343', '-0.01474', '-0.1395', '0.1647', '0.704', '-0.2742', '-0.1643', '0.3062', '0.2847', '0.3687', '0.1635', '0.7427', '-0.3618', '0.3726', '-0.6143', '0.7456', '0.2239']",C84531,,D055673,,,,
mondo:0008709,acrocephalopolydactyly,"['acrocephalopolydactylous dysplasia', 'Elejalde syndrome']",,200995,221054,CN201238,,,,C573722,,,,
mondo:0008710,RAB23-related Carpenter syndrome,"['acrocephalopolysyndactyly type 2', 'RAB23 Carpenter syndrome', 'Carpenter syndrome caused by mutation in RAB23', 'Carpenter syndrome 1', 'Carpenter syndrome type 1', 'CARPENTER syndrome 1', 'Carpenter syndrome', 'CRPT1', 'ACPS 2']",,201000,,,,,,,,,,
mondo:0008711,Goodman syndrome,"['ACPS4', 'acrocephalopolysyndactyly type IV', 'Goodman syndrome', 'ACPS 4', 'acrocephalopolysyndactyly type 4', 'Goodman camptodactyly']",,201020,65798,,,,,C537287,,,,
mondo:0008712,acrocraniofacial dysostosis,"['Kaplan Plauchu Fitch syndrome', 'acrocraniofacial dysostosis', 'Kaplan-Plauchu-Fitch syndrome']",,201050,949,C1860145,,,,C536892,,,,
mondo:0008713,acrodermatitis enteropathica,"['acrodermatitis enteropathica zinc deficiency type', 'enteropathica', 'Danbolt-Cross syndrome', 'acrodermatitis enteropathica, zinc-deficiency type', 'ae', 'Brandt syndrome', 'acrodermatitis enteropathica, zinc deficiency type', 'inherited zinc deficiency', 'AEZ']",0050605,201100,37,C0221036,"['-0.1719', '0.3013', '-0.8184', '0.1569', '-0.1026', '-0.2837', '-0.1982', '0.1859', '-0.535', '0.4263', '-0.0004573', '0.452', '-0.7036', '-0.379', '-0.9756', '0.2135', '-0.04346', '-0.1417', '-0.742', '-0.7793', '-0.949', '-0.4465', '0.3171', '-0.4841', '0.294', '-0.0463', '-0.253', '0.0702', '0.2244', '-0.716', '0.05695', '0.06683', '0.213', '0.1414', '0.2402', '0.0818', '-0.2327', '0.3535', '-0.1859', '0.2356', '0.1015', '-0.2144', '-0.3364', '0.4932', '-0.2349', '-0.2252', '-0.02051', '-0.3926', '0.8394', '0.1532', '-0.545', '-0.5737', '0.2966', '0.04517', '-0.2228', '0.2206', '0.401', '0.699', '-0.8994', '-0.7065', '-0.0652', '0.7593', '-0.00592', '-0.05362', '0.6353', '-0.1205', '0.448', '0.4814', '0.04605', '0.959', '0.0943', '-0.572', '-0.0983', '-0.4895', '-0.0477', '0.2795', '-0.1929', '-0.2272', '0.283', '0.2256', '0.5723', '-0.4177', '-0.1173', '-0.2258', '0.914', '0.2091', '-0.3904', '0.109', '0.267', '0.9443', '0.2664', '-0.01622', '-0.68', '-0.02164', '0.4329', '0.03119', '-0.435', '-0.4995', '0.3516', '-0.184']",C128802,,C538178,686.8,,,
mondo:0008714,acrofacial dysostosis Rodriguez type,"['Rodriguez lethal acrofacial dysostosis syndrome', 'acrofacial dysostosis syndrome of Rodriguez', 'acrofacial dysostosis, Rodríguez type', 'acrofacial dysostosis, syndrome of Rodriguez']",0060383,201170,1788,C1860119,,,,C538183,,,,
mondo:0008715,acrofrontofacionasal dysostosis,"['cleft Lip/palate with frontonasal dysostosis and postaxial polysyndactyly', 'acrofrontofacionasal dysostosis type 1', 'acrofrontofacionasal dysostosis 1', 'Richieri-Costa-Colletto syndrome', 'AFFN dysostosis', 'acro fronto facio nasal dysostosis', 'polysyndactyly, postaxial, frontonasal dysostosis and cleft lip/palate', 'acrofrontofacionasal dysostosis syndrome', 'polysyndactyly, postaxial, frontonasal dysostosis, and cleft Lip/palate', 'Affn dysostosis 1']",0060226,,1784,C1860118,,,,,,,,
mondo:0008716,acrogeria,"['Metageria', 'acrogeria, Gottron type', 'Gottron syndrome', 'familial acrogeria', 'acrometageria']",,201200,2500,C0406584,,,,C538187,259.8,,,
mondo:0008717,"acromesomelic dysplasia 2C, Hunter-Thompson type","['AMDH', 'acromesomelic dwarfism', 'acromesomelic dysplasia, Hunter-Thompson type', 'acromesomelic dysplasia Hunter Thompson type', 'acromesomelic dysplasia 2C, Hunter-Thompson type']",0080051,201250,968,,"['-0.1873', '0.3887', '0.184', '-0.3179', '0.476', '-0.6064', '0.1421', '0.864', '-0.486', '-0.4568', '-0.0671', '-0.02824', '-0.2363', '0.2717', '-0.1456', '0.0991', '0.5938', '0.1675', '-0.3052', '-0.3699', '-0.4412', '0.0825', '0.9795', '-0.04788', '0.255', '0.2754', '-0.0748', '-0.4155', '0.493', '0.0222', '-0.10785', '-0.3296', '-0.0328', '-0.00907', '0.3877', '-0.306', '-0.3408', '-0.4219', '-0.12177', '-0.3262', '-0.3145', '-0.771', '-0.1788', '0.0925', '-0.07654', '-0.3416', '-0.504', '0.372', '0.4858', '-0.2479', '0.1437', '-0.2045', '-0.2532', '-0.0483', '-0.5527', '-0.7144', '-0.137', '-0.7676', '-0.1777', '-0.0624', '0.3901', '0.306', '-0.2325', '0.3604', '-0.4514', '-0.3313', '-0.10767', '0.1882', '0.006203', '0.1261', '-0.1581', '0.06027', '0.1606', '-0.4966', '0.02098', '0.617', '-0.472', '0.191', '-0.4512', '-0.523', '-0.3027', '-0.1361', '0.4517', '0.281', '-0.1807', '0.4543', '-0.0423', '0.389', '0.2673', '-0.08', '-0.2255', '0.2737', '-0.02588', '0.1499', '0.525', '0.2568', '0.5366', '-0.7544', '0.04498', '0.2112']",,,,,,,
mondo:0008718,Morvan syndrome,"['Morvan^s fibrillary chorea', 'limbic encephalitis-neuromyotonia-hyperhidrosis-polyneuropathy syndrome']",,,83467,C0751540,,,1001897,,,,,
mondo:0008719,"acrorenal syndrome, autosomal recessive","['acrorenal syndrome, autosomal recessive', 'Curran syndrome', 'acrorenal syndrome recessive', 'autosomal recessive acrorenal syndrome', 'acrorenal syndrome autosomal recessive']",,201310,,C0796290,,,,C535666,,,,
mondo:0008720,congenital isolated adrenocorticotropic hormone deficiency,"['ACTH deficiency, isolated', 'isolated ACTH deficiency', 'adrenocorticotropic hormone deficiency', 'congenital isolated adrenocorticotropic hormone deficiency (disease)', 'isolated adrenocorticotropic hormone deficiency', 'IAD', 'congenital isolated ACTH deficiency']",0080150,201400,199296,C0342388,"['-0.61', '0.0836', '0.2477', '-0.1627', '0.1997', '0.3918', '0.04425', '0.2416', '-0.2078', '-0.3953', '-0.1766', '-0.1826', '0.08966', '0.1761', '-0.2693', '-0.227', '0.2651', '0.01735', '-0.3306', '-0.5605', '0.12244', '-0.4167', '0.353', '-0.1307', '0.269', '-0.1154', '-0.0927', '-0.2522', '0.0451', '-0.0624', '0.3103', '0.11615', '0.3716', '0.5547', '-0.2786', '-0.138', '-0.12085', '0.3083', '-0.1335', '-0.1215', '0.0941', '-0.01195', '0.1334', '-0.1969', '0.1164', '-0.5195', '0.2698', '-0.04233', '0.25', '0.516', '-0.05316', '0.0962', '0.2119', '0.2009', '-0.6177', '0.2583', '0.09924', '-0.3665', '-0.3394', '0.2272', '-0.0175', '0.1656', '0.2416', '-0.3652', '-0.2517', '0.145', '0.4688', '0.3142', '-0.5137', '0.006214', '-0.0699', '0.2996', '0.3552', '-0.1205', '-0.0567', '0.02861', '0.3887', '-0.0954', '-0.03714', '-0.088', '-0.0781', '0.2883', '-0.0951', '-0.2812', '-0.0216', '-0.0913', '0.2113', '-0.1045', '0.6997', '-0.02907', '0.3047', '0.4385', '0.05496', '-0.328', '0.452', '0.1643', '-0.04977', '-0.264', '0.006855', '0.613']",,1001979,C535668,255.41,,,0011748
mondo:0008721,medium chain acyl-CoA dehydrogenase deficiency,"['Mcadh deficiency', 'ACADM deficiency', 'Acyl-CoA dehydrogenase, medium chain, deficiency of', 'acyl-CoA dehydrogenase medium chain deficiency of', 'MCADD', 'Carnitine deficiency secondary to medium-chain acyl-CoA dehydrogenase deficiency', 'medium chain acyl CoA dehydrogenase deficiency', 'medium-chain acyl-Coenzyme A dehydrogenase deficiency', 'medium-chain acyl-CoA dehydrogenase deficiency', 'MCAD deficiency', 'Carnitine deficiency secondary to medium-chain acyl-Coa dehydrogenase deficiency', 'MCAD', 'ACADMD', 'medium chain acyl-coenzyme A dehydrogenase deficiency', 'acyl-CoA dehydrogenase, medium-chain deficiency', 'acyl-CoA dehydrogenase, medium-chain, deficiency OF']",0080153,201450,42,C0220710,"['0.4285', '0.367', '-0.7925', '0.09485', '-0.1715', '-0.1958', '0.04138', '0.8804', '0.2253', '-0.2042', '0.2322', '-0.1486', '0.357', '0.2488', '-0.155', '-0.1586', '-0.04736', '-0.4243', '-0.1978', '-0.6606', '0.1265', '-0.278', '1.07', '-0.2402', '-0.5137', '-0.7163', '-0.734', '0.2169', '-0.1362', '-0.4722', '0.634', '0.323', '0.226', '0.2366', '-0.8594', '-0.065', '0.03114', '0.2316', '-0.356', '-0.01791', '-0.0629', '-0.9053', '0.6553', '-0.1375', '-0.11053', '0.0479', '0.10333', '0.0589', '-0.1132', '0.86', '-0.365', '-0.0914', '0.055', '-0.4368', '0.6406', '-0.3242', '0.1936', '0.0607', '0.4895', '0.63', '-0.3022', '0.2983', '0.6885', '-0.2316', '-0.003765', '0.2267', '0.814', '0.01373', '-0.4224', '0.2754', '-0.3328', '0.2404', '-0.6646', '-0.3477', '-0.009155', '0.2842', '0.601', '-0.2355', '-0.4766', '-0.06775', '0.08594', '-0.562', '-0.275', '-0.4163', '0.439', '0.6416', '-0.3474', '-0.4255', '0.746', '-0.08813', '0.3098', '-0.11523', '0.02507', '-0.02339', '0.3584', '0.499', '0.2258', '-0.3923', '-0.2544', '-0.06934']",C84538,,C536038,277.85,E71.311,,
mondo:0008722,short chain acyl-CoA dehydrogenase deficiency,"['Acads deficiency', 'acyl-CoA dehydrogenase, short-chain, deficiency OF', 'acyl-CoA dehydrogenase, short-chain deficiency', 'SCAD deficiency', 'Scadh deficiency', 'short-chain acyl-Coenzyme A dehydrogenase deficiency (SCAD)', 'short-chain acyl-CoA dehydrogenase deficiency', 'short-chain acyl-CoA dehydrogenase deficiency (SCAD)', 'lipid-storage myopathy secondary to short-chain acyl-Coa dehydrogenase deficiency', 'ACADS deficiency', 'Scad deficiency', 'SCADD', 'short-chain acyl-coenzyme A dehydrogenase deficiency', 'SCAD', 'ACADSD']",0080154,201470,26792,,"['0.1796', '0.3367', '0.0914', '0.0899', '0.2637', '-0.3457', '-0.05933', '0.5454', '-0.2766', '-0.348', '-0.2905', '-0.4194', '0.5386', '0.5513', '-0.2551', '-0.2566', '-0.1438', '-0.2089', '-0.562', '-0.9155', '-0.3699', '-0.0868', '0.6904', '0.1318', '-0.10114', '-0.5874', '-0.2096', '-0.1951', '0.1814', '-0.3274', '0.5947', '0.1772', '0.557', '0.082', '-0.789', '0.10846', '-0.3438', '-0.4194', '-0.3086', '0.2374', '-0.3542', '-0.527', '0.2421', '-0.1554', '-0.2979', '-0.1549', '0.2593', '-0.3164', '0.3088', '0.4019', '-0.2208', '-0.4626', '0.2318', '-0.1366', '0.1406', '-0.4658', '0.3533', '-0.316', '-0.2135', '0.4917', '0.1335', '-0.188', '0.4062', '0.1248', '-0.2369', '0.3926', '0.12427', '0.2847', '-0.598', '0.0868', '0.0912', '0.4792', '-0.2238', '-0.1602', '0.2527', '0.47', '0.2411', '-1.053', '-0.1663', '0.2383', '0.6274', '0.4065', '-0.1649', '0.0592', '0.4302', '1.002', '-0.1238', '-0.07007', '0.6187', '-0.1864', '0.3486', '0.3535', '-0.7036', '-0.0888', '0.01933', '0.6484', '0.2527', '0.3328', '-0.0999', '-0.1189']",C84539,,C537596,,E71.312,,
mondo:0008723,very long chain acyl-CoA dehydrogenase deficiency,"['acyl-CoA dehydrogenase, very long-chain, deficiency OF', 'very long-chain acyl-CoA dehydrogenase deficiency', 'acyl-CoA dehydrogenase, very long-chain deficiency', 'VLCADD', 'VLCAD', 'VLCAD deficiency', 'ACADVLD', 'very long-chain acyl-Coenzyme A dehydrogenase deficiency']",0080155,201475,26793,C3887523,"['0.124', '0.2908', '-1.079', '0.5215', '-0.004185', '-0.4785', '0.0792', '0.5884', '-0.00436', '-0.2191', '0.3235', '-0.1674', '-0.04013', '-0.02962', '-0.7676', '0.1552', '-0.445', '-0.7163', '-0.7017', '-0.7095', '0.02272', '-0.74', '0.592', '0.03812', '-0.373', '-0.07355', '-0.3462', '-0.093', '0.03', '-0.4614', '1.136', '0.4324', '0.512', '0.2952', '-0.689', '-0.3574', '-0.569', '-0.02196', '-0.1244', '0.32', '-0.1079', '-0.751', '0.8755', '0.3423', '-0.01686', '-0.2234', '-0.3464', '0.1064', '-0.3093', '0.4138', '-0.493', '0.0224', '0.1783', '0.1051', '0.3132', '-0.8877', '0.2328', '0.1321', '0.736', '0.3506', '0.3403', '0.3083', '0.2852', '-0.6133', '-0.3833', '0.465', '0.6646', '0.2896', '-0.6445', '0.0486', '-0.302', '0.3357', '0.02455', '-0.1432', '0.5024', '0.10974', '0.06995', '-0.344', '0.149', '-0.01991', '0.2656', '-0.1869', '-0.224', '-0.04474', '0.508', '1.062', '-0.3413', '-0.448', '0.755', '-0.1288', '0.4648', '0.0827', '-0.367', '0.2815', '0.266', '0.5938', '0.5537', '-0.2145', '-0.67', '-1.063']",C98647,,,,E71.310,,
mondo:0008724,"adducted thumbs-arthrogryposis syndrome, Christian type",['adducted thumbs syndrome'],,201550,2952,,,,,,,,,
mondo:0008725,congenital lipoid adrenal hyperplasia due to STAR deficency,"['congenital adrenal hyperplasia lipoid', 'lipoid adrenal hyperplasia', 'CLAH', 'lipoid congenital adrenal hyperplasia', 'adrenal hyperplasia 1', 'LCAH', 'lipoid hyperplasia, congenital, of adrenal cortex with Male pseudohermaphroditism']",,201710,90790,C0342474,"['-0.675', '0.2192', '-0.5063', '-0.041', '0.2249', '-0.4258', '-0.1606', '0.3164', '-0.43', '-0.562', '0.003944', '-0.309', '-0.3228', '0.514', '-0.0321', '-0.3894', '-0.02133', '0.3809', '-0.5264', '-0.821', '-0.4822', '-0.2328', '0.8696', '0.03946', '0.5273', '-0.4907', '0.1246', '0.0399', '0.343', '-1.078', '0.5757', '0.105', '0.6157', '0.05823', '-0.4211', '0.1043', '0.07446', '0.14', '-0.6494', '0.2319', '0.2732', '-0.1744', '0.0869', '-0.0844', '0.04236', '0.004063', '-0.11', '-0.1593', '-0.1927', '0.7456', '0.445', '-0.11035', '0.03087', '-0.3008', '-0.57', '-0.1943', '0.4912', '-0.086', '0.0884', '0.52', '0.2336', '0.1164', '0.4475', '0.318', '0.1271', '-0.09784', '0.258', '0.6255', '-0.05487', '0.02034', '-0.198', '0.3052', '0.2834', '0.1195', '-0.172', '-0.2722', '0.3848', '0.2123', '-0.3313', '-0.1409', '-0.1361', '0.2137', '-0.2847', '-0.3545', '0.5503', '0.0829', '-0.004135', '-0.4043', '0.2065', '-0.3162', '0.1079', '0.7134', '-0.08325', '-0.5825', '0.4944', '-0.008545', '0.333', '-0.7427', '-0.3608', '-0.1823']",,,,,,,
mondo:0008726,Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis,"['Antley-Bixler syndrome with genital anomalies and disordered steroidogenesis', 'ABS1', 'Antley-Bixler syndrome with genital anomaly and disorder of steroidogenesis']",,201750,63269,C3150099,,C178415,,,,,,
mondo:0008727,congenital adrenal hyperplasia due to 3-beta-hydroxysteroid dehydrogenase deficiency,"['adrenal hyperplasia, congenital, due to 3-BETA-hydroxysteroid dehydrogenase 2 deficiency', '3-BETA-hydroxysteroid dehydrogenase, type II, deficiency OF', '3-Beta-HSD deficiency', '3-beta HSD deficiency', 'CAH due to 3-beta-hydroxysteroid dehydrogenase deficiency', '3b-hydroxysteroid dehydrogenase deficiency', 'adrenal hyperplasia II', 'type II 3-beta-hydroxysteroid dehydrogenase deficiency', 'adrenal hyperplasia, congenital, due to 3-Beta-hydroxysteroid dehydrogenase 2 deficiency', 'HSD3B deficiency', '3-Beta-hydroxysteroid dehydrogenase deficiency', 'adrenal hyperplasia 2']",,201810,90791,,"['-1.165', '0.5938', '-0.8555', '-0.149', '0.378', '-0.28', '-0.9604', '1.516', '-0.3567', '-0.831', '0.58', '-0.12427', '0.1345', '1.91', '-0.4282', '0.12244', '0.165', '0.3196', '-0.5776', '-0.4744', '-0.2047', '0.1917', '0.1195', '0.252', '0.5166', '0.143', '-0.0716', '0.1587', '0.9688', '-0.847', '0.4492', '0.1375', '0.544', '0.0976', '-0.01938', '0.434', '0.005646', '0.2355', '-0.02309', '-0.4436', '0.2257', '-0.2944', '0.05554', '-0.4568', '0.00823', '-1.165', '-0.07745', '-0.01889', '0.4116', '0.768', '0.2534', '-0.546', '0.02173', '-0.7266', '-0.2139', '-0.2925', '-0.0968', '-0.8384', '-0.0474', '0.3633', '-0.2532', '0.04788', '0.9634', '-0.1555', '0.678', '1.168', '0.3677', '0.436', '-0.1373', '0.1797', '-0.6343', '0.8735', '-0.162', '-0.1636', '-0.02992', '-0.651', '-0.3726', '-0.1134', '-0.4824', '-0.147', '0.251', '0.08514', '0.0695', '-0.656', '0.9067', '0.4985', '0.06223', '-1.022', '0.7095', '0.1461', '0.3306', '0.2314', '-0.07', '-0.1233', '0.4778', '0.403', '0.08984', '-0.351', '0.1423', '0.04672']",C131088,,C538236,,,,
mondo:0008728,classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency,"['adrenal hyperplasia, congenital, due to 21-hydroxylase deficiency', 'hyperandrogenism, Nonclassic type, due to 21-Hydroxylase deficiency', 'congenital adrenal hyperplasia 1', '21-hydroxylase deficiency', 'congenital adrenal hyperplasia due to 21-hydroxylase deficiency', 'CYP21 deficiency', '21 hydroxylase deficiency', 'adrenal hyperplasia, congenital, due to 21-HYDROXYLASE deficiency', 'adrenal hyperplasia 3', '21-OHD', 'classic 21-OHD CAH']",,201910,90794,C4273964,"['-0.672', '0.573', '-0.8145', '-0.1499', '0.06555', '-0.1534', '-0.5166', '1.607', '-0.276', '-0.6797', '0.1043', '-0.03406', '-0.2098', '2.354', '-0.617', '0.3218', '-0.0875', '0.3691', '-0.3696', '-0.4175', '0.05304', '0.12067', '0.404', '-0.1346', '0.319', '0.2983', '-0.04898', '0.25', '1.151', '-0.7524', '0.572', '0.1074', '0.4468', '0.1565', '0.2064', '0.962', '-0.01578', '0.1412', '-0.07574', '-0.2856', '0.2617', '-0.1621', '-0.02263', '-0.379', '0.2155', '-0.9033', '-0.1599', '0.2375', '0.04984', '0.543', '-0.01239', '-0.5786', '0.3777', '-0.627', '0.00899', '-0.02812', '-0.1847', '-0.629', '-0.2722', '0.3118', '-0.1963', '0.3096', '0.8843', '-0.1542', '0.5493', '0.6904', '0.3357', '0.212', '-0.4495', '0.314', '-0.1255', '0.3838', '0.395', '-0.704', '0.1849', '-0.7876', '-0.571', '-0.2487', '-0.4365', '-0.2764', '0.4534', '0.1919', '-0.02705', '-0.782', '0.4294', '0.2384', '0.2808', '-0.8867', '0.539', '0.4736', '-0.03226', '0.527', '-0.1064', '-0.013855', '0.2559', '0.1796', '0.355', '-0.335', '0.04315', '0.281']",C131087,,C535979,,,,
mondo:0008729,congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency,"['adrenal hyperplasia 4', 'CAH due to 11-beta-hydroxylase deficiency', 'adrenal hyperplasia, hypertensive form', 'steroid 11-Beta-Hydroxylase deficiency', 'P450C11B1 deficiency', 'adrenal hyperplasia, congenital, due to steroid 11-BETA-HYDROXYLASE deficiency', 'adrenal hyperplasia hypertensive form', 'adrenal hyperplasia, congenital, due to 11-beta-hydroxylase deficiency', '11-Beta-Hydroxylase deficiency', 'adrenal hyperplasia IV', 'CYP11B1 deficiency']",,202010,90795,C0268292,"['-0.9634', '0.48', '-0.945', '-0.3225', '0.1462', '-0.2122', '-0.912', '1.584', '-0.4675', '-1.145', '0.465', '0.0919', '0.04468', '1.889', '-0.5483', '0.2291', '0.09454', '0.216', '-0.509', '-0.4094', '-0.095', '-0.06665', '0.08575', '-0.11316', '0.37', '0.3076', '-0.05444', '-0.111', '1.285', '-0.56', '0.3628', '0.13', '0.5913', '0.1527', '-0.05807', '0.4927', '-0.3074', '0.2247', '0.181', '-0.425', '0.3179', '-0.2365', '0.1221', '-0.3857', '0.007225', '-0.799', '0.00724', '0.02003', '0.5586', '0.635', '0.1926', '-0.495', '-0.01895', '-0.6143', '0.1146', '-0.1891', '-0.1948', '-0.7407', '-0.1273', '0.3892', '-0.0927', '0.356', '0.9023', '-0.359', '0.687', '1.125', '0.2307', '0.1832', '-0.4917', '0.2434', '-0.7056', '0.4976', '-0.1959', '-0.04132', '0.0233', '-0.5737', '-0.5273', '-0.2634', '-0.5967', '-0.1836', '0.303', '0.03378', '0.1271', '-0.8555', '0.609', '0.387', '0.3235', '-0.4272', '0.724', '0.2754', '0.371', '0.371', '-0.313', '0.1089', '0.525', '0.205', '0.368', '-0.4749', '0.2262', '0.00419']",C131085,,C535978,277.6,,10000002,
mondo:0008730,congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency,"['17,20-lyase deficiency, isolated', 'CAH due to 17-alpha-hydroxylase deficiency', '17-Alpha-Hydroxylase/17,20-lyase deficiency, combined partial', '17-Alpha-Hydroxylase deficiency', 'adrenal hyperplasia, congenital, due to 17-ALPHA-HYDROXYLASE deficiency', '17-Alpha-Hydroxylase/17,20-lyase deficiency, combined complete', 'congenital adrenal hyperplasia type 5', 'combined 17-hydroxylase/17,20-lyase deficiency', 'adrenal hyperplasia 5', '17-alpha-hydroxylase/17,20-lyase deficiency']",,202110,90793,,"['-0.9453', '0.4434', '-0.968', '-0.4753', '0.158', '-0.2336', '-0.871', '1.52', '-0.335', '-0.944', '0.3716', '-0.0673', '0.00658', '1.922', '-0.3853', '0.06647', '0.13', '0.508', '-0.3755', '-0.7314', '-0.0925', '-0.10126', '0.04663', '-0.2593', '0.4421', '0.3052', '-0.1002', '-0.01785', '1.156', '-0.4487', '0.4382', '0.1068', '0.4265', '0.0859', '0.03397', '0.623', '-0.11', '0.2306', '0.2961', '-0.4568', '0.4539', '-0.05185', '0.03143', '-0.5', '0.01185', '-0.8276', '-0.02782', '-0.003149', '0.5444', '0.6577', '0.2617', '-0.533', '-0.0445', '-0.472', '-0.10205', '0.01165', '-0.06714', '-0.575', '-0.04648', '0.353', '-0.1113', '0.2036', '1.018', '-0.474', '0.4797', '1.206', '0.338', '0.3857', '-0.4482', '0.3645', '-0.7197', '0.5454', '-0.1035', '-0.291', '-0.01862', '-0.5503', '-0.495', '-0.289', '-0.3872', '-0.238', '0.4656', '-0.06186', '0.1873', '-0.9854', '0.7017', '0.1981', '-0.04782', '-0.6553', '0.754', '0.4873', '0.4912', '0.3416', '-0.05173', '0.1067', '0.71', '0.11316', '0.172', '-0.46', '0.0897', '0.1093']",,,,277.6,,,
mondo:0008731,familial adrenal hypoplasia with absent pituitary luteinizing hormone,"['adrenal hypoplasia, congenital, with absent pituitary luteinizing hormone', 'familial adrenal hypoplasia with absent pituitary LH', 'familial adrenal hypoplasia, miniature type']",,202150,95700,C1859978,,,,C565976,,,,
mondo:0008732,"adrenal hypoplasia, cytomegalic type","['adrenal hypoplasia, cytomegalic type']",,202155,,C1859977,,,,,,,,
mondo:0008733,familial glucocorticoid deficiency,"['glucocorticoid deficiency', 'GCCD']",0080620,,361,CN204661,"['0.1362', '-0.087', '0.165', '-0.213', '0.1958', '-0.2208', '-0.2507', '0.6235', '-0.2097', '-0.00955', '0.00525', '0.0972', '-0.1737', '0.0893', '-0.2952', '0.11127', '-0.02203', '-0.2698', '-0.1315', '-0.5938', '0.3962', '-0.3718', '0.2742', '-0.1726', '0.04926', '0.1627', '-0.3418', '0.1875', '-0.05453', '-0.409', '0.07715', '-0.161', '0.2305', '0.2607', '-0.4485', '0.2491', '-0.1399', '0.1233', '-0.4844', '0.4055', '-0.00764', '-0.2015', '0.2712', '0.05743', '0.306', '-0.01755', '-0.5396', '-0.1359', '-0.2227', '1.306', '0.2421', '-0.003416', '0.2166', '-0.1332', '0.1124', '0.193', '0.4463', '-0.1718', '-0.4678', '1.044', '-0.1103', '0.5615', '0.363', '-0.588', '0.1771', '0.4888', '0.2479', '0.05692', '-0.5522', '0.007153', '-0.1647', '-0.2394', '-0.05563', '-0.38', '0.1664', '0.03317', '0.2573', '-0.3298', '0.1649', '0.01576', '0.1182', '-0.0573', '-0.3418', '-0.1414', '0.0937', '0.4253', '0.3074', '-0.02084', '0.792', '-0.03494', '0.2489', '-0.03069', '0.305', '-0.292', '0.471', '0.279', '0.3574', '-0.651', '0.2208', '-0.05276']",C120446,,C565974,,,,
mondo:0008734,"adrenocortical carcinoma, hereditary","['adrenocortical carcinoma, pediatric', 'adrenocortical carcinoma, hereditary', 'adrenocortical carcinoma, paediatric', 'ADCC', 'hereditary adrenal cortex carcinoma']",,202300,,C1859972,"['-0.006992', '0.03128', '-0.00968', '-0.01552', '0.005642', '-0.04807', '-0.01984', '0.0552', '-0.0348', '0.009514', '0.001233', '-0.02307', '-0.008965', '0.02621', '-0.04028', '-0.0499', '0.01419', '-0.02563', '-0.010284', '-0.0865', '-0.02124', '-0.03308', '0.06616', '-0.02179', '0.03029', '0.006084', '0.003777', '-0.022', '0.00922', '-0.05966', '0.0474', '-0.01735', '0.06192', '0.01332', '0.01316', '-0.01912', '-0.02443', '-0.01776', '-0.01053', '-0.02611', '0.0162', '-0.0727', '0.04266', '-0.04523', '0.01585', '-0.04257', '-0.01796', '0.0165', '0.0201', '0.01262', '-0.0047', '0.00809', '0.011154', '0.006405', '-0.05847', '-0.001047', '0.05362', '-0.02478', '-0.0834', '-0.007175', '0.04404', '0.01496', '0.02617', '0.005005', '0.007294', '0.0191', '0.08624', '0.0669', '-0.04922', '0.07367', '-0.02678', '-0.003008', '0.02306', '-0.0276', '0.0467', '0.01642', '-0.005947', '0.00724', '-0.03598', '-0.04437', '-0.02292', '0.012146', '-0.0396', '0.02507', '-0.01852', '-0.01872', '0.02495', '0.0212', '0.06134', '-0.006664', '0.0406', '0.03305', '0.01184', '0.00884', '0.11273', '0.01236', '0.0557', '-0.0704', '-0.02544', '0.0352']",,,C565972,,,,
mondo:0008735,adrenocortical unresponsiveness to ACTH with postreceptor defect,"['adrenocortical unresponsiveness to ACTH with postreceptor defect', 'familial glucocorticoid deficiency due to defect distal to ACTH receptor']",,202355,,C1859971,,,,C565971,,,,
mondo:0008736,peroxisome biogenesis disorder 2B,"['PBD2B', 'peroxisome biogenesis disorder 2B', 'peroxisome biogenesis disorder type 2B']",0080622,202370,,C3550234,,C155751,,,,,,
mondo:0008737,congenital afibrinogenemia,"['hypofibrinogenemia, congenital', 'afibrinogenemia, congenital', 'factor I deficiency', 'familial afibrinogenemia', 'fibrinogen deficiency', 'afibrinogenemia', 'afibrinogenemia congenital']",2236,202400,98880,,"['-0.2756', '0.02992', '-0.3198', '-0.6343', '-0.1526', '0.1289', '0.1205', '0.2189', '-0.0753', '0.3086', '-0.1855', '0.001344', '-0.1427', '0.04147', '-0.02998', '-0.0999', '0.2233', '-0.011055', '-0.00942', '-0.6973', '-0.372', '-0.1378', '0.485', '-0.2888', '-0.03702', '-0.0646', '0.1837', '0.06476', '0.1036', '0.000333', '0.1705', '0.08307', '0.4395', '0.4683', '-0.292', '-0.0917', '-0.1349', '-0.3066', '0.1156', '-0.241', '-0.0328', '-0.1311', '0.369', '-0.12415', '0.2343', '-0.06573', '-0.1748', '0.1116', '0.2917', '0.2178', '0.5557', '-0.1416', '0.1066', '-0.04565', '-0.3086', '0.0004365', '0.2634', '-0.03445', '-0.4697', '-0.09735', '-0.1823', '0.282', '0.272', '-0.4204', '0.1864', '0.1504', '0.298', '-0.02733', '-0.3767', '0.24', '-0.478', '-0.00925', '-0.421', '-0.614', '0.2825', '0.2217', '1.065', '0.1787', '-0.005173', '-0.2175', '-0.6025', '0.05096', '0.0637', '0.1052', '0.2402', '-0.002432', '0.3203', '0.4575', '0.1685', '-0.55', '0.154', '0.705', '0.1426', '-0.328', '0.727', '0.273', '0.574', '-0.2744', '-0.1239', '0.2532']",C98130,,D000347,,,,
mondo:0008738,"aganglionosis, total intestinal","['aganglionosis, total intestinal', 'total intestinal aganglionosis']",,202550,,,,C101074,,C538058,,,,
mondo:0008739,agenesis of cerebral white matter,['agenesis of cerebral white matter'],,202600,,,,,,,,,,
mondo:0008740,agnathia-otocephaly complex,"['agnathia-holoprosencephaly', 'agnathia-holoprosencephaly-situs inversus syndrome', 'AGOTC', 'agnathia-otocephaly complex', 'otocephaly', 'Dysgnathia Complex agnathia-holoprosencephaly', 'holoprosencephaly-agnathia', 'dysgnathia complex agnathia-holoprosencephaly']",0060341,202650,990,CN207252,"['-0.0633', '0.1316', '0.5107', '-0.4387', '0.1697', '-0.0746', '-0.1754', '0.002964', '-0.5957', '-0.2903', '-0.545', '-0.4424', '0.00475', '-0.06964', '-0.311', '-0.0259', '0.0805', '-0.2625', '-0.359', '-0.253', '-0.11017', '-0.0949', '0.4033', '-0.321', '0.2416', '-0.006496', '-0.03041', '0.4104', '0.628', '-0.3877', '-0.04745', '0.4094', '0.535', '0.2228', '0.4033', '-0.01851', '0.3628', '-0.3125', '-0.4495', '-0.7856', '-0.1732', '-0.181', '-0.148', '-0.678', '-0.1202', '-0.324', '0.1921', '0.645', '-0.2218', '0.1627', '-0.002134', '-0.3916', '-0.2046', '-0.07745', '-1.169', '-0.05753', '0.04874', '-0.06793', '-0.4905', '0.639', '-0.369', '0.2825', '-0.2156', '0.09094', '-0.537', '-0.0771', '0.562', '0.0812', '-0.6987', '0.2852', '-0.2411', '0.353', '0.2234', '0.03162', '0.03049', '0.1803', '0.315', '0.03882', '-0.4956', '-0.196', '-0.0685', '-0.10114', '0.347', '0.509', '0.0467', '-0.5547', '-0.067', '0.583', '0.2617', '-0.3252', '-0.0338', '0.4314', '0.722', '-0.04764', '0.3103', '-0.0675', '0.458', '-0.39', '0.1235', '0.4287']",C124568,,,759.89,,,
mondo:0008741,PAGOD syndrome,"['pulmonary hypoplasia-agonadism-dextrocardia-diaphragmatic hernia syndrome', 'PAGOD syndrome', 'agonadism with multiple internal malformations', 'Kennerknecht sorgo Oberhoffer syndrome', 'pulmonary hypoplasia, hypoplasia of the pulmonary artery, agonadism, omphalocele-diaphragmatic defect, and dextrocardia']",,202660,991,C1859967,,,,C537018,,,,
mondo:0008742,autosomal dominant severe congenital neutropenia,"['severe congenital neutropenia, autosomal dominant', 'severe congenital neutropenia autosomal dominant']",0112130,,486,C1859966,"['-0.1584', '0.1204', '-0.1143', '-0.03087', '0.2776', '-0.2426', '0.01399', '0.2793', '-0.02808', '-0.2502', '-0.1942', '-0.0478', '0.2908', '-0.1614', '0.301', '0.0576', '0.0824', '0.4053', '0.01353', '-0.4868', '-0.1461', '0.0405', '0.3342', '-0.4663', '0.2196', '-0.1202', '-0.2183', '-0.2054', '-0.301', '-0.367', '0.172', '0.2798', '0.2998', '0.1205', '-0.387', '0.1716', '-0.3657', '-0.4126', '-0.2225', '-0.183', '-0.1597', '-0.02963', '0.0717', '-0.2085', '-0.082', '-0.3718', '-0.4004', '0.08246', '0.1853', '0.01439', '0.0738', '-0.1672', '0.11774', '0.01508', '-0.0998', '-0.0626', '0.2396', '0.0547', '-0.2063', '0.1031', '-0.08435', '0.2146', '0.05646', '-0.1625', '0.11664', '-0.2423', '0.1204', '0.3513', '-0.4365', '0.2352', '-0.2373', '-0.08844', '-0.02495', '-0.2756', '0.2668', '-0.2764', '0.1508', '0.11487', '0.0782', '0.04996', '-0.3547', '-0.02098', '-0.11505', '-0.01566', '0.2075', '0.12164', '0.4124', '0.3462', '0.0778', '0.0468', '0.02003', '0.3782', '-0.1632', '0.03586', '0.6694', '0.5127', '0.5156', '-0.4194', '-0.2186', '0.02754']",C166155,,,,,,
mondo:0008743,Stimmler syndrome,"['Alaninuria with microcephaly, dwarfism, enamel hypoplasia and diabetes mellitus', 'ALANINURIA with microcephaly, dwarfism, enamel hypoplasia, and diabetes mellitus', 'Stimmler syndrome']",,202900,3199,C1859965,,,,C565968,,,,
mondo:0008744,alar cartilages hypoplasia-coloboma-telecanthus syndrome,"['coloboma of alar-nasal cartilages with telecanthus', 'alar-nasal cartilages, coloboma of, with telecanthus', 'frontonasal dysplasia with alar clefts']",,203000,2007,C1859964,,,,C535967,,,,
mondo:0008745,oculocutaneous albinism type 1A,"['oculocutaneous albinism caused by mutation in Tyr', 'OCA1A', 'albinism, oculocutaneous, type IA', 'albinism 1', 'oculocutaneous albinism, type 1', 'Tyr oculocutaneous albinism', 'oculocutaneous albinism type IA', 'oculocutaneous albinism, tyrosinase-negative', 'tyrosinase-negative oculocutaneous albinism', 'albinism, oculocutaneous, type 1A', 'TYR oculocutaneous albinism']",0070094,203100,79431,,"['0.3057', '0.10864', '-0.3186', '0.00157', '0.494', '-0.08484', '-0.2546', '0.4768', '0.03192', '-0.6006', '0.4346', '-0.2029', '0.2434', '0.8477', '-0.5376', '0.398', '0.4463', '-0.2505', '0.4526', '-0.7295', '-0.8013', '0.1947', '0.76', '-0.511', '-0.1288', '-0.1945', '-0.595', '-0.10175', '0.6206', '0.2158', '0.482', '0.2498', '0.307', '0.6084', '0.1335', '0.402', '-0.943', '-0.577', '0.4172', '-0.1381', '1.233', '0.05884', '-0.3315', '0.02113', '-0.2123', '-0.6646', '0.573', '-1.019', '0.8594', '0.171', '0.02501', '-0.5474', '0.05914', '-0.228', '0.3445', '0.3372', '0.2642', '1.068', '0.01455', '-0.8667', '-0.1831', '0.4404', '0.6104', '0.561', '0.06216', '0.2773', '0.3828', '0.6274', '-0.195', '0.636', '-0.02419', '0.3406', '0.0449', '-0.2026', '0.6465', '0.2578', '-0.03041', '-0.3176', '-0.02618', '-0.372', '0.7593', '-0.535', '0.257', '0.4663', '-0.4893', '-1.518', '0.5024', '0.7812', '0.8833', '0.3396', '-0.00494', '0.8496', '-0.2054', '-0.1428', '0.548', '0.2917', '-0.3608', '-0.3489', '0.4302', '0.4104']",C168731,,,270.2,,,
mondo:0008746,oculocutaneous albinism type 2,"['albinism, oculocutaneous, type II, modifier of', 'Albinoidism', 'oculocutaneous albinism tyrosinase positive', 'tyrosinase-positive oculocutaneous albinism', 'Brown oculocutaneous albinism', 'oculocutaneous albinism, tyrosinase-positive', 'albinism, oculocutaneous, type II', 'albinism 2', 'albinism, oculocutaneous, type 2', 'oculocutaneous albinism, type 2', 'OCA2', 'oculocutaneous albinism type II', 'albinism, Brown oculocutaneous']",0070096,203200,79432,C0268495,"['0.2856', '-0.02063', '-0.357', '0.2438', '0.5337', '-0.004543', '-0.2651', '0.489', '-0.1456', '-0.4626', '0.611', '-0.2434', '0.0665', '0.5986', '-0.2854', '0.3364', '0.6235', '-0.1702', '0.4658', '-0.7676', '-0.797', '0.0564', '0.665', '-0.5938', '-0.26', '-0.4412', '-0.635', '0.0466', '0.584', '0.1921', '0.4353', '-0.01314', '0.441', '0.5903', '-0.0851', '0.327', '-0.4946', '-0.81', '0.3877', '-0.2369', '1.481', '-0.1635', '-0.3157', '-0.1583', '-0.3035', '-0.741', '0.6523', '-0.8774', '0.7827', '0.3462', '-0.2108', '-0.4146', '0.0496', '-0.3342', '0.4658', '0.37', '0.10803', '1.084', '-0.00842', '-0.815', '-0.2112', '0.1192', '0.4412', '0.3591', '-0.1852', '0.3472', '0.596', '0.58', '-0.03323', '0.693', '-0.015015', '0.4775', '0.126', '-0.2427', '0.6836', '0.2932', '-0.08984', '-0.3193', '0.1364', '-0.467', '0.8843', '-0.654', '0.178', '0.518', '-0.3042', '-1.349', '0.397', '0.5015', '0.891', '0.3843', '0.1829', '1.028', '-0.2383', '-0.02818', '0.3215', '0.4312', '-0.3643', '-0.252', '0.2947', '0.3892']",,,C537730,,,,
mondo:0008747,oculocutaneous albinism type 3,"['albinism, oculocutaneous, type III', 'Red oculocutaneous albinism', 'albinism, oculocutaneous, type 3', 'rufous oculocutaneous albinism', 'xanthous oculocutaneous albinism', 'TYRP1 oculocutaneous albinism', 'ROCA', 'oculocutaneous albinism type III', 'albinism 3', 'rufous OCA', 'Xanthism', 'oculocutaneous albinism, type 3', 'oculocutaneous albinism caused by mutation in TYRP1', 'OCA3']",0070097,278400,79433,,"['0.3208', '-0.0743', '-0.4922', '0.088', '0.5146', '0.1489', '-0.324', '0.509', '-0.208', '-0.5576', '0.5664', '-0.2827', '0.06757', '0.9717', '-0.3682', '0.4673', '0.4048', '-0.1948', '0.3376', '-0.5923', '-0.6914', '0.08606', '0.6846', '-0.6025', '-0.3188', '-0.3508', '-0.9404', '-0.0786', '0.587', '0.09674', '0.231', '-0.11237', '0.2134', '0.3738', '0.04132', '0.2627', '-0.679', '-0.805', '0.2986', '-0.4517', '1.452', '-0.1526', '-0.4204', '-0.06232', '-0.1255', '-0.554', '0.439', '-0.9277', '0.715', '0.1841', '-0.04077', '-0.544', '0.01744', '-0.1544', '0.402', '0.2222', '0.477', '0.8833', '-0.1444', '-0.801', '-0.2471', '0.33', '0.774', '0.4998', '0.07', '0.4993', '0.3086', '0.541', '-0.05756', '0.5063', '-0.2256', '0.332', '0.04694', '-0.011696', '0.7075', '0.4458', '0.1716', '-0.315', '0.2294', '-0.1732', '0.7935', '-0.62', '0.3591', '0.775', '-0.3875', '-1.346', '0.7783', '0.759', '1.036', '0.3494', '0.1835', '1.362', '-0.3127', '-0.08307', '0.6694', '0.2808', '-0.3796', '-0.1844', '0.4106', '0.1731']",,,C537731,270.2,,,
mondo:0008748,Hermansky-Pudlak syndrome 1,"['Hermansky-Pudlak syndrome caused by mutation in HPS1', 'HPS1', 'albinism with hemorrhagic diathesis and pigmented reticuloendothelial cells', 'Hermansky-Pudlak syndrome 1', 'HPS1 Hermansky-Pudlak syndrome', 'Delta storage pool disease', 'Hermansky-Pudlak syndrome type 1']",0060539,203300,,C2931875,,C150367,,C538539,,,,
mondo:0008749,pseudohypoparathyroidism type 2,"['PHP II', 'pseudohypoparathyroidism, type II', 'PHP2', 'Php 2']",,203330,94090,CN206737,,,,C548077,275.49,,,
mondo:0008750,microcephaly-albinism-digital anomalies syndrome,"['microcephaly-albinism-digital anomalies syndrome', 'Castro Gago-Pombo-Novo syndrome', 'albinism-microcephaly digital anomalies syndrome', 'albinism-microcephaly-digital anomalies syndrome']",,203340,2513,C1859910,,,,C537322,,,,
mondo:0008751,corticosterone methyloxidase type 1 deficiency,"['18-Hydroxylase deficiency', 'hyperreninemic hypoaldosteronism, familial, 1', 'aldosterone deficiency due to defect in steroid 18-Hydroxylase', 'corticosterone methyloxidase type I deficiency', '18 alpha hydroxylase deficiency', 'corticosterone methyloxidase type 1 deficiency', 'aldosterone deficiency 1', 'steroid 18-hydroxylase deficiency', '18 Hydroxylase deficiency', 'CMO 1 deficiency', 'aldosterone deficiency due to defect in 18 hydroxylase', 'hypoaldosteronism, congenital, due to cmo i deficiency']",0080626,203400,,CN074214,,,,,,,,
mondo:0008752,Alexander disease,"['megalencephaly in infancy accompanied by progressive spasticity and dementia', 'ALXDRD', 'AxD', 'alexanders leukodystrophy', 'Alexander^s disease', 'Alexander disease']",4252,203450,58,C0270726,"['-0.1661', '0.4668', '-0.2126', '0.00724', '-0.1321', '-0.787', '0.08856', '0.4734', '-0.6196', '0.6436', '-0.466', '-0.2476', '0.2166', '-0.1547', '0.7524', '-0.1301', '-0.2625', '-0.6475', '-0.1191', '-0.4265', '0.2114', '-0.10675', '0.6133', '0.1583', '0.514', '0.003332', '-0.1892', '-0.2303', '-0.628', '-0.03778', '0.485', '0.534', '0.3472', '-0.06555', '0.2732', '-0.0854', '-0.2756', '-0.06775', '-0.2129', '-0.3284', '0.1688', '-0.437', '-0.02768', '0.3198', '0.3354', '-0.324', '-0.06183', '-0.0502', '-0.6934', '-0.4385', '0.568', '0.311', '-0.6475', '-0.671', '-0.08276', '-0.09607', '0.8276', '-0.0761', '-0.2673', '0.4048', '-0.2573', '0.2435', '0.497', '0.02464', '-0.355', '0.3982', '0.547', '0.1289', '-0.3152', '0.4792', '0.174', '0.359', '0.4263', '0.1578', '0.4163', '-0.09375', '-0.1868', '-0.1492', '-0.191', '-0.283', '0.01671', '-0.05237', '-0.2032', '0.1365', '0.1482', '0.05087', '0.1522', '0.1967', '0.6875', '-0.405', '0.12317', '0.00856', '0.0769', '-0.02646', '0.288', '0.553', '0.5234', '-0.0821', '-0.06006', '0.0691']",C84545,,D038261,,,,
mondo:0008753,alkaptonuria,"['homogentisic acidura', 'homogentisic acid oxidase deficiency', 'alkaptonuria', 'hereditary ochronosis', 'ochronosis, hereditary', 'alkaptonuric ochronosis', 'homogentisate 1,2-dioxygenase deficiency', 'alcaptonuria', 'deficiency of homogentisicase', 'aku']",9270,203500,56,C2931645,"['-0.2052', '0.1559', '-0.008865', '0.509', '0.422', '-0.2583', '-0.1993', '0.81', '-0.4807', '0.32', '-0.5728', '0.0353', '0.0335', '0.952', '-0.6284', '0.2651', '-0.2883', '-0.2715', '-0.1923', '-0.917', '-0.1791', '-0.468', '0.6465', '-0.2805', '-0.881', '-0.2109', '-0.0845', '0.709', '-0.2954', '-0.05942', '0.5854', '-0.11554', '-0.10956', '0.2588', '0.01222', '-0.4426', '0.07654', '-0.3547', '0.3906', '-0.174', '-0.1847', '-0.5386', '0.5283', '0.0872', '0.2184', '-0.05954', '0.837', '0.1212', '-0.02043', '0.4023', '-0.03574', '-0.02954', '0.5254', '-0.6753', '0.2289', '-0.3826', '0.263', '0.214', '0.1703', '-0.263', '0.9106', '0.09894', '-0.659', '0.514', '0.04648', '-0.1174', '0.992', '0.641', '0.474', '-0.189', '-0.239', '-0.242', '-0.6836', '-0.01799', '-0.0877', '0.807', '0.1152', '0.1578', '0.1381', '-0.6196', '0.0613', '0.001948', '0.3115', '0.508', '-0.527', '0.036', '-0.2119', '-0.2417', '0.01599', '0.06323', '0.405', '0.3154', '-0.15', '-0.01643', '-0.1202', '0.0036', '0.302', '-0.1069', '0.089', '0.1115']",C84546,,D000474,270.2,,10001689,
mondo:0008754,alopecia - contractures - dwarfism - intellectual disability syndrome,"['ACD mental retardation syndrome', 'alopecia-contractures-dwarfism mental retardation syndrome', 'alopecia-contractures-dwarfism intellectual disability syndrome', 'ACD-intellectual disability syndrome', 'ACD intellectual disability syndrome']",,203550,1005,C0795895,,,,C537051,,,,
mondo:0008755,Moynahan syndrome,"['alopecia epilepsy oligophrenia syndrome of Moynahan', 'alopecia-epilepsy-oligophrenia syndrome of Moynahan', 'Moynahan alopecia syndrome', 'alopecia-epilepsy-intellectual disability syndrome, Moynahan type']",,203600,2574,,,,,C537052,,,,
mondo:0008756,alopecia - intellectual disability syndrome,"['alopecia with severe intellectual deficit', 'Perniola-Krajewska-Carnevale syndrome', 'Amr syndrome', 'alopecia-intellectual disability syndrome', 'AMR syndrome 1', 'alopecia intellectual disbility syndrome 1', 'alopecia-mental retardation syndrome']",0080627,,2850,,"['0.4253', '-0.00752', '0.4573', '-0.3289', '0.4907', '-0.309', '0.333', '0.634', '-0.1515', '-0.4414', '-0.2166', '-0.4138', '-0.2192', '-0.1672', '0.0693', '-0.11505', '0.805', '-0.2424', '-0.1137', '-0.9434', '0.10034', '-0.1676', '0.04007', '-0.561', '0.3406', '0.12225', '-0.4348', '-0.04623', '0.231', '-0.1299', '0.4666', '-0.335', '0.114', '0.4468', '-0.3125', '-0.0237', '-0.28', '-0.2057', '-0.1737', '0.0824', '-0.02638', '0.1569', '-0.02931', '-0.6094', '0.384', '-0.4893', '-0.084', '0.09784', '-0.4995', '0.2751', '-0.1989', '0.251', '0.03012', '-0.1722', '0.00758', '-0.1355', '0.1179', '-0.524', '-0.3289', '0.04575', '-0.05475', '0.2389', '0.4087', '-0.03564', '-0.1191', '-0.12335', '0.1478', '0.2104', '-0.3533', '0.2352', '-0.2832', '0.4854', '0.2795', '-0.818', '0.225', '0.0781', '0.3167', '0.11847', '-0.1017', '0.2764', '0.211', '0.25', '0.378', '0.7896', '0.473', '0.06696', '0.1573', '0.7656', '0.0836', '0.689', '0.617', '0.704', '-0.1813', '0.3552', '0.6016', '0.4597', '0.4932', '-0.3726', '0.5537', '0.3335']",,,,,,,
mondo:0008757,alopecia universalis congenita,"['AU', 'atrichia, generalized', 'alopecia universalis congenita', 'atrichia, generalised', 'alopecia universalis', 'alopecia areata universalis', 'ALUNC']",0050634,203655,701,C0263505,,,,C537055,704.09,,10001767,
mondo:0008758,mitochondrial DNA depletion syndrome 4a,"['Alper^s syndrome', 'Alper^s disease', 'PNDC', 'MTDPS4A', 'Poliodystrophia cerebri progressiva', 'Alpers progressive infantile poliodystrophy', 'progressive cerebral poliodystrophy', 'Alpers Huttenlocher disease', 'diffuse cerebral degeneration in infancy', 'Alpers diffuse Degeneration of cerebral Grey matter with hepatic cirrhosis', 'Alpers disease', 'Alpers diffuse Degeneration of cerebral Gray matter with hepatic cirrhosis', 'mitochondrial DNA depletion syndrome type 4a', 'Alpers syndrome', 'Alper syndrome', 'Alpers-Huttenlocher syndrome', 'AHS', 'mitochondrial DNA depletion syndrome 4A', 'mitochondrial DNA depletion syndrome 4A (Alpers type)', 'infantile poliodystrophy', 'Alpers^ disease or gray-matter degeneration', 'progressive neuronal degeneration of childhood with liver disease', 'Alpers Huttenlocher syndrome', 'neuronal Degeneration of childhood with liver disease, progressive', 'AHD', 'Alpers progressive sclerosing poliodystrophy', 'progressive sclerosing poliodystrophy']",1442,203700,726,C0205710,"['0.3572', '0.293', '0.1816', '-0.04355', '-0.3357', '-0.3748', '0.732', '0.926', '-0.2678', '0.2104', '-0.3328', '-0.3176', '-0.4365', '0.3645', '0.3052', '-0.5654', '-0.1292', '-0.831', '0.1202', '-0.9224', '-0.2837', '-0.706', '0.08887', '-0.06186', '-0.0995', '-0.376', '-0.2384', '0.1978', '-0.2229', '0.2167', '0.2468', '0.02702', '0.4644', '-0.332', '0.0431', '0.01688', '-0.4453', '-0.3474', '-0.5', '0.427', '-0.381', '-0.549', '0.2032', '0.574', '0.0967', '-0.347', '-0.6377', '-0.757', '0.0664', '0.8467', '-0.2725', '0.6475', '-0.1732', '-0.3582', '0.391', '0.00485', '0.418', '0.2003', '-0.619', '-0.05386', '0.2778', '0.1445', '0.845', '-0.1302', '-0.1073', '-0.4219', '0.5283', '-0.229', '0.1178', '0.4658', '0.01283', '-0.04068', '-0.5273', '-0.0333', '0.00243', '-0.3035', '0.4258', '-0.15', '-0.2725', '0.1858', '-0.468', '-0.1858', '-0.4182', '0.11017', '-0.3179', '0.3035', '0.3433', '0.2595', '0.5034', '0.4956', '0.3835', '0.3909', '-0.3838', '-0.04028', '-0.1504', '0.1648', '0.5137', '-0.263', '0.2175', '0.1162']",C35257,,,330.8,,10062943,
mondo:0008759,oxoglutaricaciduria,"['Alpha KGD deficiency', '2-ketoglutarate dehydrogenase deficiency', 'ALPHA-ketoglutarate dehydrogenase deficiency', 'Alpha-Kgd deficiency', 'oxoglutarate dehydrogenase deficiency', 'Oxoglutaric aciduria', 'Alpha-ketoglutarate dehydrogenase deficiency', '2 alpha ketoglutarate dehydrogenase deficiency']",0081326,203740,31,C2752074,,,,C536582,,,,
mondo:0008760,beta-ketothiolase deficiency,"['Alpha-methyl-acetoacetyl-CoA thiolase deficiency', 'peroxisomal thiolase deficiency', 'mitochondrial acetoacetyl-Coa thiolase deficiency', 'alpha-methylacetoaceticaciduria', '2-Methyl-3-hydroxybutyric acidemia', 'Mat deficiency', 'mitochondrial acetoacetyl-CoA thiolase deficiency', 'Beta ketothiolase deficiency', '3-Ktd deficiency', '3-oxothiolase deficiency', 'beta-ketothiolase deficiency', 'mitochondrial acetoacetyl-coenzyme A thiolase deficiency', 'Alpha methylacetoacetic aciduria', 'ALPHA-methylacetoacetic aciduria', '3-ketothiolase deficiency', '2-methyl-3-hydroxybutyricacidemia', 'T2 deficiency', 'BKT']",14723,203750,134,C1533628,"['0.2075', '0.1941', '-0.83', '0.0961', '0.0807', '-0.303', '0.10724', '0.512', '-0.501', '-0.2043', '-0.4607', '-0.3184', '0.499', '0.1438', '-0.1655', '0.1321', '-0.11194', '-0.7427', '-0.2227', '-0.777', '-0.3472', '-0.426', '0.583', '0.05313', '-0.2295', '-0.4592', '-0.2798', '-0.339', '-0.134', '0.01243', '0.1993', '0.47', '0.2886', '0.10767', '-1.001', '0.1443', '-0.2812', '-0.005985', '0.0702', '-0.2385', '-0.002512', '-0.1553', '0.6445', '0.1268', '-0.3604', '-0.1791', '0.07654', '0.02707', '0.3496', '1.058', '-0.4443', '0.06824', '0.02872', '-0.456', '0.69', '0.1077', '0.437', '0.1449', '-0.1282', '0.5664', '0.3005', '0.578', '0.705', '-0.5576', '-0.0858', '-0.1708', '0.332', '0.553', '-0.64', '0.2086', '-0.5483', '0.04028', '-0.2239', '-0.2488', '0.4785', '0.366', '0.2422', '-0.0692', '-0.05893', '-0.2964', '0.2125', '-0.519', '0.4055', '-0.2742', '0.5205', '0.4712', '-0.3435', '0.02727', '0.526', '0.4524', '0.6104', '0.287', '-0.24', '0.00262', '-0.2922', '0.6396', '0.23', '-0.318', '-0.5283', '0.1454']",C98841,,C535434,,,,
mondo:0008762,autosomal recessive Alport syndrome,"['Alport syndrome autosomal recessive', 'Alport syndrome recessive type', 'Alport syndrome 2, autosomal recessive', 'Alport syndrome, autosomal recessive', 'nephropathy and deafness']",0110033,203780,88919,,"['0.3135', '0.04944', '-0.1985', '-0.1592', '-0.004673', '-0.4504', '-0.2308', '0.1653', '-0.4197', '-0.3064', '-0.12317', '-0.245', '-0.3076', '0.3772', '-0.0699', '-0.359', '-0.1342', '-0.1973', '0.2678', '-0.2532', '-0.09894', '-0.2258', '0.2316', '0.2205', '0.493', '-0.2754', '-0.2595', '-0.1669', '0.1414', '0.366', '0.3022', '0.01726', '0.3687', '-0.1561', '0.113', '-0.2085', '0.02008', '-0.02745', '0.1438', '0.0813', '-0.2925', '0.02405', '0.04236', '0.2107', '-0.282', '-0.4185', '-0.316', '-0.3735', '0.2435', '0.1136', '0.1425', '-0.05896', '0.4402', '-0.58', '0.4028', '-0.4587', '0.3423', '0.2284', '-0.4028', '0.01483', '0.1844', '-0.3853', '0.2688', '0.1785', '-0.1473', '-0.287', '0.2383', '0.539', '-0.318', '0.2986', '-0.301', '-0.1721', '0.1995', '0.1667', '0.4905', '-0.001248', '0.1438', '0.5366', '-0.0883', '0.1815', '0.2756', '-0.1236', '0.0211', '0.5415', '-0.4602', '-0.1832', '0.473', '0.04834', '0.0316', '0.6562', '-0.1058', '0.2021', '-0.09', '0.3', '0.6187', '0.2114', '0.3687', '-0.4358', '-0.07886', '0.367']",,,,,,10001843,
mondo:0008763,Alstrom syndrome,"['Alstrom^s syndrome', 'ALSS', 'ALMS', 'Alström syndrome', 'Alstrom syndrome']",0050473,203800,64,C0268425,"['-0.286', '-0.3223', '-0.05038', '0.35', '-0.0367', '-0.8403', '0.1478', '0.7505', '-0.1661', '-0.6416', '0.0829', '-0.2368', '-0.5713', '-0.09424', '-0.5327', '-0.5547', '0.1536', '0.0969', '0.4146', '-0.1902', '-0.03583', '-0.403', '0.1732', '-0.1026', '0.1076', '-0.1882', '-0.33', '0.442', '0.3071', '-0.3667', '1.822', '-0.1981', '0.274', '-0.06024', '-0.3464', '0.16', '-0.04538', '-0.2369', '-0.3179', '-0.3938', '-0.1812', '0.2406', '0.85', '0.2102', '-0.4578', '-0.1642', '0.1225', '0.01707', '-0.334', '0.1453', '-0.751', '0.612', '0.331', '0.07635', '-0.03604', '-0.2725', '0.2314', '-0.566', '-0.1465', '-0.1516', '-0.2869', '0.1586', '-0.1383', '-0.0762', '-0.41', '0.02812', '-0.12494', '0.3267', '0.03134', '-0.1155', '-0.7114', '-0.399', '0.3638', '0.0736', '0.648', '0.1185', '0.2693', '-0.5522', '-0.292', '0.2448', '0.3452', '-0.029', '-0.843', '-0.1469', '-0.4233', '0.8774', '0.7334', '-0.2068', '0.2408', '0.587', '0.1305', '0.3845', '0.05145', '0.1414', '0.2133', '-0.1451', '0.314', '-0.7837', '0.002867', '-0.00946']",C84549,,D056769,759.89,,10068783,
mondo:0008764,Leber congenital amaurosis 1,"['Leber congenital amaurosis caused by mutation in GUCY2D', 'amaurosis congenita of Leber I', 'amaurosis congenita of Leber, type 1', 'LCA1', 'amaurosis congenita of Leber 1', 'Leber congenital amaurosis type 1', 'LCA', 'retinal blindness, congenital', 'GUCY2D Leber congenital amaurosis', 'CRB', 'Leber congenital amaurosis 1']",0110078,204000,,,,,,,,H35.5,,
mondo:0008765,Leber congenital amaurosis 2,"['RPE65 Leber congenital amaurosis', 'amaurosis congenita of Leber II', 'Leber congenital amaurosis 2', 'LCA2', 'Leber congenital amaurosis type 2', 'amaurosis congenita of Leber 2', 'amaurosis congenita of Leber, type 2', 'Leber congenital amaurosis caused by mutation in RPE65']",0110016,204100,,C1859844,,,,C536601,,H35.5,,
mondo:0008766,amaurosis-hypertrichosis syndrome,"['amaurosis congenita cone-rod type with congenital hypertrichosis', 'amaurosis congenita, cone-rod type, with congenital hypertrichosis']",,204110,1021,,,,,C536604,,H35.5,,
mondo:0008767,neuronal ceroid lipofuscinosis 3,"['CLN3 disease, juvenile', 'CLN3 neuronal ceroid lipofuscinosis', 'ceroid lipofuscinosis, neuronal, type 3', 'batten disease', 'Spielmeyer Sjogren disease', 'Spielmeyer-Sjogren disease', 'ceroid lipofuscinosis, neuronal, 3', 'CLN3 disease', 'neuronal ceroid lipofuscinosis caused by mutation in CLN3', 'neuronal ceroid lipofuscinosis type 3', 'Vogt Spielmeyer disease', 'Vogt-Spielmeyer disease', 'neuronal ceroid lipofuscinosis, juvenile', 'CLN3']",0110731,204200,228346,,"['0.2294', '0.64', '-0.2856', '0.1112', '0.4785', '-1.188', '0.002958', '0.3462', '-0.2411', '0.1917', '-0.6797', '-0.0848', '0.01563', '-0.08496', '0.4878', '-0.6265', '-0.1823', '-0.4902', '0.265', '-0.1566', '0.2817', '-0.2937', '0.014824', '-0.2245', '0.0991', '-0.2961', '-0.469', '-0.2642', '-0.6963', '0.2534', '0.986', '-0.3394', '0.593', '-0.2595', '0.608', '0.1418', '-0.9336', '0.4126', '-0.5044', '0.01898', '-0.1602', '-0.2281', '0.994', '-0.07117', '0.0673', '-0.99', '-0.2021', '0.02777', '0.1448', '0.2385', '0.741', '0.4817', '-0.9565', '-0.03662', '0.6636', '-1.402', '0.9814', '-0.3484', '-0.369', '0.02266', '0.2507', '0.02702', '0.354', '-0.0762', '0.6924', '-0.2856', '0.7827', '0.00954', '-0.29', '0.4055', '-0.2131', '0.2996', '-0.0242', '-0.7944', '0.283', '0.3816', '0.10266', '0.2115', '-0.771', '-0.0333', '0.6006', '0.411', '-0.649', '0.1765', '0.5244', '-0.4512', '0.1731', '0.969', '-0.179', '0.1624', '0.11176', '0.253', '-0.6387', '0.07764', '0.335', '0.1577', '0.5195', '-0.11487', '0.5493', '-0.2122']",C61258,,,,,,
mondo:0008768,"ceroid lipofuscinosis, neuronal, 6B (Kufs type)","['Kuf^s disease, autosomal recessive', 'CLN6 neuronal ceroid lipofuscinosis', 'neuronal ceroid lipofuscinosis caused by mutation in CLN6', 'Kuf^s disease type A', 'neuronal ceroid lipofuscinosis 4A', 'autosomal recessive neuronal ceroid lipofuscinosis 4A', 'neuronal ceroid lipofuscinosis type 4A', 'ceroid lipofuscinosis, neuronal, 4A, autosomal recessive', 'CLN4A disease', 'adult neuronal ceroid lipofuscinosis 4A', 'CLN4A']",0110730,204300,228340,,"['-0.1901', '0.2778', '0.2362', '0.016', '-0.08014', '-0.2805', '-0.1621', '0.012024', '-0.2472', '-0.00708', '-0.3743', '-0.2223', '-0.2181', '0.01295', '0.1979', '-0.343', '-0.357', '0.02069', '-0.14', '-0.3542', '0.1898', '-0.297', '0.1525', '0.06915', '-0.01915', '-0.0794', '-0.0969', '0.147', '-0.2345', '0.09283', '0.1719', '0.2015', '0.349', '-0.1393', '0.2415', '0.0632', '-0.2378', '-0.001058', '0.02524', '-0.1803', '-0.03345', '-0.3904', '0.1207', '0.2058', '0.000584', '-0.455', '0.1917', '0.1163', '0.08997', '0.1908', '0.2205', '0.3914', '-0.1305', '-0.04327', '0.1037', '-0.552', '0.317', '0.0918', '-0.4224', '0.05948', '0.1643', '0.01659', '0.314', '0.002598', '-0.07385', '0.0163', '0.1666', '0.2379', '-0.271', '0.0642', '-0.2988', '-0.04132', '0.0184', '-0.1027', '0.26', '0.1034', '-0.002705', '0.2644', '-0.1255', '-0.0888', '-0.1439', '-0.492', '-0.07745', '0.2522', '0.0607', '-0.2622', '0.2734', '0.02693', '0.09827', '-0.0342', '0.2593', '0.0325', '-0.03516', '-0.0121', '0.551', '0.3682', '0.3445', '-0.2035', '0.0722', '0.2286']",,,,,,,
mondo:0008769,neuronal ceroid lipofuscinosis 2,"['CLN2', 'neuronal ceroid lipofuscinosis, late infantile', 'ceroid lipofuscinosis, neuronal, type 2', 'TPP1 neuronal ceroid lipofuscinosis', 'CLN2 disease', 'Jansky-Bielschowsky disease', 'ceroid lipofuscinosis, neuronal, 2, variable Age at onset', 'CLN2 disease, juvenile (subtype)', 'late infantile neuronal ceroid lipofuscinosis', 'CLN2 disease, late infantile (subtype)', 'neuronal ceroid lipofuscinosis caused by mutation in TPP1', 'neuronal ceroid lipofuscinosis 2 variable age at onset', 'ceroid lipofuscinosis, neuronal, 2', 'neuronal ceroid lipofuscinosis type 2']",0110726,204500,228349,,"['-0.2974', '0.4705', '-0.05963', '-0.01431', '0.2822', '-0.4446', '-0.1957', '-0.112', '-0.335', '-0.2218', '0.03928', '0.05032', '0.1766', '-0.2544', '0.1611', '-0.12115', '-0.06604', '-0.1785', '-0.0751', '-0.625', '0.1492', '-0.06174', '0.5234', '0.02629', '0.01186', '-0.004433', '0.0878', '-0.05423', '-0.02826', '-0.1958', '0.2247', '0.1853', '0.2205', '0.031', '0.1063', '-0.1858', '-0.0792', '-0.04553', '-0.3538', '-0.4802', '0.0388', '-0.3801', '0.1064', '0.10706', '-0.01978', '-0.5166', '0.07135', '0.0543', '0.5176', '0.2395', '0.0315', '0.10016', '-0.1775', '-0.1654', '0.081', '-0.7603', '0.4392', '0.234', '-0.2896', '0.2244', '0.2058', '0.1844', '0.3748', '-0.008545', '0.05032', '0.181', '0.1676', '0.07196', '-0.557', '0.01654', '-0.2461', '-0.1649', '0.09235', '0.2428', '0.2898', '0.3171', '0.2186', '0.4766', '-0.3364', '-0.1249', '0.1826', '-0.1725', '-0.09534', '0.207', '-0.0869', '-0.3374', '0.1785', '0.2654', '0.2615', '-0.1029', '0.2632', '0.07965', '-0.188', '-0.2598', '0.5576', '0.2338', '0.3123', '-0.2898', '-0.1472', '0.106']",C85864,,,,,,
mondo:0008770,amelogenesis imperfecta type 1C,"['amelogenesis imperfecta, local hypoplastic type, autosomal recessive', 'amelogenesis imperfecta, type 1C', 'amelogenesis imperfecta, type IC', 'autosomal recessive amelogenesis imperfecta hypoplastic with or without openbite malocclusion', 'autosomal recessive amelogenesis imperfecta local hypoplastic type', 'amelogenesis imperfecta, hypoplastic, with or without Openbite malocclusion, autosomal recessive', 'AI1C', 'amelogenesis imperfecta type IC']",0110056,204650,,C2673923,,,,C567147,,,,
mondo:0008771,amelogenesis imperfecta type 1G,"['enamel-renal-gingival syndrome', 'absent enamel, nephrocalcinosis and apparently normal calcium metabolism', 'generalized enamel hypoplasia and renal dysfunction', 'amelogenesis imperfecta type IG', 'amelogenesis imperfecta hypoplastic type, IG', 'amelogenesis imperfecta, hypoplastic, with nephrocalcinosis', 'generalised enamel hypoplasia and renal dysfunction', 'AI1G', 'enamel renal syndrome', 'amelogenesis imperfecta hypoplastic with nephrocalcinosis', 'amelogenesis imperfecta and nephrocalcinosis', 'amelogenesis imperfecta nephrocalcinosis', 'amelogenesis imperfecta, type IG (enamel-renal syndrome)', 'amelogenesis imperfecta, type IG', 'ers', 'enamel-renal syndrome', 'FAM20A amelogenesis imperfecta', 'amelogenesis imperfecta-gingival hyperplasia syndrome', 'amelogenesis imperfecta caused by mutation in FAM20A', 'amelogenesis imperfecta and gingival fibromatosis syndrome', 'AIGFS', 'amelogenesis imperfecta-nephrocalcinosis syndrome']",0110066,614253,171836,CN200302,"['0.1508', '-0.1171', '0.5015', '-0.3667', '-0.1249', '0.01984', '-0.444', '0.6606', '-0.06366', '0.1825', '-0.6514', '-0.5063', '-0.82', '0.3894', '-0.1792', '-0.1866', '-0.002943', '-0.1749', '0.04346', '-0.861', '-0.2039', '-0.2368', '0.4727', '-0.10986', '0.47', '-0.08', '-0.6006', '0.0918', '-8.7e-05', '-0.445', '-0.0781', '0.0891', '0.12415', '0.3286', '0.2036', '-0.1589', '0.0563', '-0.2245', '-0.04337', '-0.0749', '0.1768', '0.1401', '0.4321', '-0.194', '-0.3315', '-0.186', '-0.1854', '0.2402', '0.1036', '0.0753', '0.3953', '0.1062', '0.6406', '-0.2659', '-0.4424', '-0.327', '0.4238', '-0.4177', '-0.5938', '0.269', '0.4514', '-0.0587', '-0.1111', '-0.559', '0.431', '-0.5474', '0.672', '0.619', '-0.02707', '0.3303', '-0.4373', '-0.1937', '0.2998', '-0.3167', '0.3513', '-0.4802', '0.02473', '0.1654', '0.02905', '0.02734', '-0.3606', '-0.0261', '0.1875', '0.1862', '0.1348', '0.1626', '0.03342', '-0.621', '0.78', '0.3228', '0.1847', '0.8276', '-0.11804', '0.1628', '0.1207', '0.05405', '0.5293', '-0.1864', '-0.07117', '0.4536']",,,C538241,520.5,,,
mondo:0008772,amelogenesis imperfecta type 2A1,"['amelogenesis imperfecta caused by mutation in KLK4', 'KLK4 amelogenesis imperfecta', 'amelogenesis imperfecta type IIA1', 'amelogenesis imperfecta, type IIA1', 'amelogenesis imperfecta pigmented hypomaturation type 1', 'amelogenesis imperfecta, hypomaturation type, IIA1', 'amelogenesis imperfecta, pigmented hypomaturation type, 1', 'AI2A1', 'amelogenesis imperfecta pigmented hypomaturation type']",0110057,204700,,,,,,C567146,,,,
mondo:0008773,"amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis, and acidosis","['amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis, and acidosis', 'amino aciduria with mental deficiency, dwarfism, muscular dystrophy, osteoporosis and acidosis']",,204730,,C1859818,,,,C565960,,,,
mondo:0008774,2-aminoadipic 2-oxoadipic aciduria,"['Ketoadipicaciduria', 'alpha-aminoadipic aciduria', '2-aminoadipic 2-oxoadipic aciduria', 'AMOXAD', 'alpha-aminoadipic and alpha-ketoadipic aciduria']",0111453,245130,79154,C1855626,"['-0.1287', '0.0758', '-0.0763', '-0.1437', '-0.04486', '-0.3618', '0.003056', '0.2715', '-0.3994', '0.002491', '-0.315', '-0.1752', '0.0927', '-0.1852', '0.1262', '-0.148', '0.012375', '-0.11383', '-0.3484', '-0.513', '-0.009575', '-0.012405', '0.1627', '-0.2207', '0.1103', '-0.11566', '-0.09766', '-0.1877', '0.12476', '-0.1149', '0.02971', '0.03824', '0.3877', '0.2966', '-0.2458', '-0.0926', '-0.3525', '-0.3257', '-0.2913', '-0.1328', '0.3394', '-0.3687', '0.06085', '-0.04343', '-0.0333', '-0.3928', '0.01614', '0.0524', '-0.1392', '0.233', '-0.2303', '0.3042', '-0.0917', '-0.138', '0.0384', '0.1648', '0.0987', '-0.1998', '-0.1234', '0.1569', '0.3503', '0.02945', '0.354', '0.1403', '-0.1207', '0.04175', '0.1855', '0.2617', '-0.1263', '0.2847', '-0.1364', '0.182', '-0.2607', '-0.0143', '-0.03455', '0.1968', '0.2515', '-0.2527', '-0.07355', '-0.1087', '0.1228', '-0.1442', '-0.252', '0.384', '0.2747', '0.3176', '-0.0864', '0.1573', '0.3645', '0.1349', '0.2192', '0.4514', '-0.1921', '-0.07495', '0.5146', '0.2725', '0.2673', '-0.2615', '0.346', '0.2786']",,,C565453,,,,
mondo:0008775,"Amobarbital, deficient N-hydroxylation of","['Amobarbital, deficient N-hydroxylation of']",,204800,,C1859816,,,,C565959,,,,
mondo:0008776,"amyloidosis of gingiva and conjunctiva, with intellectual disability","['amyloidosis of gingiva and conjunctiva with intellectual disability', 'amyloidosis of gingiva and conjunctiva, with mental retardation', 'amyloidosis of gingiva and conjunctiva with mental retardation', 'Hornova Dlushosova syndrome', 'amyloidosis of gingiva and conjunctiva, with intellectual disability']",,204850,,C1859815,,,,C565958,,,,
mondo:0008777,gelatinous drop-like corneal dystrophy,"['corneal dystrophy, gelatinous drop-like', 'corneal amyloidosis', 'amyloid corneal dystrophy, Japanese type', 'CDGDL', 'amyloidosis corneal', 'lattice corneal dystrophy type 3', 'gelatinous drop-like corneal dystrophy', 'subepithelial amyloidosis of the cornea', 'Cdgdl', 'primary familial amyloidosis of the cornea', 'GDLD', 'lattice corneal dystrophy, type 3', 'amyloidosis, corneal', 'corneal dystrophy, lattice type 3', 'GDCD']",0060449,204870,98957,C0339273,"['-0.498', '-0.1177', '-0.4734', '0.4177', '0.4248', '-0.446', '-0.4697', '0.3164', '-0.1637', '-0.5137', '-0.1774', '-0.389', '-0.115', '0.4104', '-0.2192', '-0.39', '-0.07196', '-0.577', '0.0759', '-0.572', '-0.561', '-0.1315', '0.2413', '0.2153', '-0.371', '0.3303', '-0.6685', '-0.1792', '-0.6265', '0.167', '1.089', '0.0698', '-0.12476', '-0.1299', '0.1376', '0.01276', '-0.3267', '-0.2166', '0.438', '-0.0765', '0.1915', '-0.6787', '0.04865', '0.0971', '0.02982', '0.73', '0.2996', '-0.4275', '-0.426', '0.687', '0.454', '0.4897', '0.314', '-0.2422', '-0.1573', '0.06152', '0.3755', '-0.06586', '-0.519', '-0.2356', '0.401', '-0.5054', '-0.1129', '0.4153', '-0.01098', '0.12115', '0.8076', '0.765', '-0.3271', '0.478', '-0.348', '-0.662', '0.3003', '0.0812', '0.516', '0.7124', '0.1545', '-0.01307', '-0.0288', '-0.2063', '0.1389', '-0.1991', '-0.08514', '0.4185', '-0.1981', '-0.629', '-0.3564', '0.3838', '-0.1486', '-0.1514', '0.251', '0.441', '0.1118', '0.0846', '0.1693', '-0.0617', '0.3435', '-0.4834', '0.2896', '0.4016']",C142805,,C535480,,,,
mondo:0008778,"amyloidosis, cutaneous bullous","['amyloidosis, cutaneous bullous']",,204900,,C0268399,,,,C562644,277.39,,,
mondo:0008779,arthrogryposis,"['Arthrogryposes, congenital multiple', 'congenital multiple Arthrogryposes', 'congenital multiple arthrogryposis']",,,,C0003886,,C84572,0003857,D001176,,,,
mondo:0008780,"amyotrophic lateral sclerosis type 2, juvenile","['amyotrophic lateral sclerosis caused by mutation in ALS2', 'ALS, juvenile', 'ALS2', 'ALS2 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis 2', 'amyotrophic lateral sclerosis 2, juvenile']",0060194,205100,,,,,,C565957,,,,
mondo:0008781,juvenile amyotrophic lateral sclerosis with dementia,"['ALS-dementia Complex', 'amyotrophic lateral sclerosis, juvenile, with dementia', 'ALS-dementia complex']",0110067,205200,,C1859806,,,,C565956,,,,
mondo:0008782,amyotrophic lateral sclerosis with polyglucosan bodies,['amyotrophic lateral sclerosis with polyglucosan bodies'],,205250,,C1859805,,,,C565955,,,,
mondo:0008783,Tangier disease,"['Alpha high density lipoprotein deficiency disease', 'familial high density lipoprotein deficiency', 'A-alphalipoprotein neuropathy', 'cholesterol thesaurismosis', 'high density lipoprotein deficiency, Tangier type', 'high density lipoprotein deficiency, type 1', 'ATP-binding cassette transporter A1 deficiency', 'Analphalipo-proteinemia', 'defective adenosine triphosphate-binding cassette transporter A1', 'HDLDT1', 'familial high density lipoprotein deficiency disease', 'Analphalipoproteinemia', 'familial Hypoalphalipo-proteinemia', 'HDL lipoprotein deficiency disease', 'familial alpha-lipoprotein deficiency', 'tgd', 'Tangier disease']",1388,205400,31150,C0039292,"['0.1592', '0.275', '-0.4216', '-0.3667', '0.04596', '-0.359', '-0.3826', '0.4314', '0.4612', '0.07776', '-0.3457', '-0.006622', '0.2175', '0.187', '-0.234', '-0.2174', '-0.0002005', '-0.05084', '-0.2534', '-0.5547', '0.0727', '-0.3838', '0.2688', '-0.1853', '-0.02046', '0.3625', '0.2412', '0.767', '0.008095', '-0.2483', '1.273', '0.3862', '-0.2642', '-0.0677', '-0.4175', '-0.4983', '0.072', '0.1611', '0.0709', '-0.724', '-0.2827', '-0.3906', '0.5005', '-0.4395', '-0.1448', '-0.03555', '0.379', '-0.1807', '-0.10657', '0.233', '0.0662', '0.02148', '-0.331', '0.1616', '-0.1694', '-0.461', '0.0634', '-0.531', '-0.3333', '0.1095', '-0.341', '0.362', '-0.1683', '-0.8247', '-0.4128', '-0.07025', '0.2216', '1.063', '0.3452', '0.11224', '-0.3376', '-0.5713', '-1.046', '0.3408', '0.4016', '0.1552', '-0.1631', '0.2832', '0.3733', '-0.7886', '-1.084', '-0.507', '-0.295', '0.557', '-0.2471', '0.003496', '-0.0624', '0.12476', '0.3518', '0.10297', '0.24', '0.3774', '0.2462', '0.1687', '1.066', '0.1017', '0.11206', '0.02277', '-0.07526', '-0.4812']",C85182,,D013631,,,10051875,
mondo:0008785,sideroblastic anemia 2,"['SIDBA2', 'pyridoxine refractory sideroblastic anaemia', 'pyridoxine refractory sideroblastic anemia', 'anemia, sideroblastic, 2, pyridoxine-refractory', 'sideroblastic anemia pyridoxine-refractory autosomal recessive', 'sideroblastic anaemia pyridoxine-refractory autosomal recessive', 'anemia, sideroblastic, pyridoxine-refractory, autosomal recessive']",0060065,205950,,,,,,C567145,,,,
mondo:0008786,pyridoxine-responsive sideroblastic anemia,"['sideroblastic anaemia pyridoxine-responsive autosomal recessive', 'anemia congenital sideroblastic B6-responsive', 'anaemia congenital sideroblastic B6-responsive', 'B6-responsive sideroblastic anemia', 'anemia, sideroblastic, pyridoxine-responsive, autosomal recessive', 'anemia, congenital sideroblastic, B6-responsive', 'B6-responsive sideroblastic anaemia', 'sideroblastic anemia pyridoxine-responsive autosomal recessive']",0060066,206000,,C1859787,,,,C565954,,,,
mondo:0008787,microcytic anemia with liver iron overload,"['microcytic anemia and hepatic iron overload', 'anemia, hypochromic microcytic, with iron overload 1', 'hypochromic microcytic anaemia with iron overload', 'anemia, hypochromic microcytic, with iron overload type 1', 'hypochromic microcytic anemia with iron overload', 'microcytic anaemia and hepatic iron overload', 'AHMIO1']",,206100,83642,,"['-0.3594', '0.282', '0.01796', '0.4045', '0.774', '0.1277', '-0.3235', '0.488', '-0.2612', '-0.2913', '0.6973', '-0.1793', '0.1622', '0.579', '-1.292', '0.02254', '-0.6636', '0.2983', '-0.7017', '-0.691', '-3.11e-05', '-0.6978', '0.2805', '-0.2277', '0.625', '-0.4065', '0.05948', '-0.35', '0.6343', '-0.03653', '0.1687', '0.2378', '0.4553', '0.4636', '0.1422', '-0.476', '-0.9526', '-0.613', '0.5903', '-0.11', '-0.779', '0.2505', '0.0905', '-0.3376', '-0.7295', '-0.8667', '0.2761', '0.10724', '0.3457', '-0.2295', '0.5176', '0.579', '0.968', '-0.0765', '0.4329', '-0.8135', '0.1519', '0.2703', '-0.9824', '0.2054', '-0.07306', '0.3962', '-0.274', '-0.2424', '-0.1038', '0.1973', '0.174', '0.8716', '-0.68', '0.8047', '0.8926', '-0.11285', '-0.528', '-0.687', '0.2043', '0.888', '0.1467', '0.1759', '0.2822', '0.4429', '0.09766', '0.00531', '-0.01805', '0.0831', '0.4133', '-0.2861', '-0.501', '0.2966', '0.8726', '-0.2498', '0.745', '0.229', '-0.2646', '-0.1663', '0.768', '1.068', '0.0143', '-0.10895', '0.3108', '-0.5977']",,,,,,,
mondo:0008788,IRIDA syndrome,"['iron-handling disorder, hereditary', 'pseudo-iron-deficiency Anemia', 'IRIDA', 'pseudo-iron-deficiency Anaemia', 'iron-refractory iron deficiency anaemia', 'iron-refractory iron deficiency anemia', 'anemia, hypochromic microcytic, with defect in iron metabolism']",,206200,209981,,"['-0.3503', '0.579', '-0.268', '-0.1035', '0.3474', '-0.05817', '-0.6865', '0.814', '0.01912', '-0.218', '-0.557', '0.1649', '0.1653', '0.1552', '0.141', '0.543', '0.1423', '0.1063', '-0.4807', '-0.6973', '-0.2023', '-0.729', '0.74', '0.1324', '-0.05493', '-0.1415', '0.334', '-0.327', '0.04974', '-0.4028', '0.2109', '-0.1943', '0.2052', '0.605', '-0.3123', '-0.3665', '-0.3752', '-0.4297', '0.2615', '0.258', '0.2634', '0.4197', '0.3196', '-0.1478', '-0.02701', '-1.048', '-0.0835', '-0.1658', '-0.289', '-0.0576', '0.09125', '-0.673', '-0.05865', '0.325', '0.615', '0.03082', '0.1897', '-0.10095', '-0.4978', '0.6895', '0.08484', '0.2441', '0.242', '-0.865', '-0.4248', '-0.3315', '0.0741', '0.5635', '-0.566', '0.3462', '0.076', '-0.1698', '-0.4956', '0.2283', '0.2693', '0.1967', '-0.3108', '0.3242', '-0.1716', '0.2362', '0.705', '-0.4485', '0.2854', '-0.09143', '0.05444', '0.3398', '0.02344', '0.03314', '0.534', '-0.0471', '0.7314', '0.3066', '-0.2272', '-0.303', '1.132', '0.6274', '-0.2333', '-0.6646', '0.02588', '-0.35']",,,C562385,,,,
mondo:0008789,"anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane","['anemia, nonspherocytic hemolytic, associated with abnormality of red cell membrane']",,206300,,C1859786,,,,C565953,,,,
mondo:0008790,"anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism","['anemia, nonspherocytic hemolytic, possibly due to defect in porphyrin metabolism']",,206400,,C1859785,,,,C565952,,,,
mondo:0008791,anencephaly 1,"['anencephaly 1', 'isolated anencephaly/exencephaly', 'ANPH', 'absence of a large part of the brain and the skull', 'anencephaly']",,206500,1048,,"['-0.02803', '-0.05328', '-0.0815', '0.5435', '0.5366', '-0.2903', '-0.102', '0.6733', '0.01149', '-0.3596', '-0.5366', '-0.1493', '-0.04984', '0.1027', '-0.542', '-0.3713', '0.588', '-0.607', '-0.4731', '-0.1915', '-0.05063', '-0.418', '0.5947', '0.02962', '0.1416', '-0.3052', '0.0793', '0.1556', '-0.2546', '0.0658', '0.832', '-0.05856', '0.1641', '0.1573', '-0.0312', '-0.01013', '0.303', '-0.207', '-0.0652', '0.1415', '-0.3018', '-0.479', '0.1046', '-0.699', '-0.6553', '-0.0132', '0.02927', '-0.03436', '-0.11444', '0.04456', '-0.1675', '-1.111', '-0.708', '-0.08215', '-0.615', '0.598', '-0.1316', '-0.0643', '-0.0891', '0.1656', '-0.2683', '-0.10925', '0.4521', '0.152', '-0.4116', '0.4653', '0.524', '-0.1357', '-0.6187', '0.4128', '0.316', '0.10406', '-0.141', '-0.5054', '-0.02654', '0.3818', '0.521', '-0.2054', '-0.1877', '-0.493', '-0.3057', '0.04803', '-0.08093', '0.1991', '-0.2969', '0.05914', '0.476', '0.0701', '0.08185', '-0.3179', '0.0644', '0.4941', '0.5244', '0.6675', '0.3237', '-0.2441', '-0.1221', '-0.5854', '0.1628', '-0.5767']",,,,740.0,,,
mondo:0008792,familial angiolipomatosis,"['angiolipomatosis, familial', 'angiolipoma Microthromboticum']",,206550,199279,C1859784,,,,C565951,,,,
mondo:0008793,"angiomatosis, diffuse Corticomeningeal, of Divry and van Bogaert","['Corticomeningeal angiomatosis, myelination of the white substance of the centrum ovale, hemianopsia and marbled skin', 'angiomatosis, diffuse Corticomeningeal, of Divry and van Bogaert', 'Divry-Van Bogaert syndrome']",,206570,,C1859783,,,,C536367,,,,
mondo:0008794,"anhidrosis, familial generalized, with abnormal or absent sweat glands","['anhidrosis, familial generalized, with abnormal or absent sweat glands']",,206600,,C4225670,,,,,,,,
mondo:0008795,aniridia-cerebellar ataxia-intellectual disability syndrome,"['aniridia, cerebellar ataxia and mental deficiency', 'GLSP', 'aniridia, cerebellar ataxia, and intellectual disability', 'aniridia, cerebellar ataxia, and mental retardation', 'Gillespie syndrome', 'GILLESPIE syndrome']",0111578,206700,1065,C0431401,"['-0.116', '-0.324', '0.01848', '0.0592', '-0.11554', '-0.508', '0.02425', '0.10846', '-0.549', '-0.9653', '0.0731', '0.1514', '0.02258', '0.1241', '0.4412', '-0.1295', '-0.02287', '-0.05914', '0.09326', '-0.978', '-0.1089', '-0.0477', '0.01088', '-0.3474', '0.1844', '-0.4946', '-0.1676', '0.11176', '0.01505', '-0.9194', '0.2498', '0.2861', '-0.393', '-0.1486', '0.4302', '0.1571', '-0.0759', '0.06506', '0.3467', '0.5605', '0.4758', '0.10156', '-0.3245', '0.4312', '0.4602', '-0.4521', '0.1866', '0.443', '0.2263', '-0.2437', '-0.1166', '0.2269', '0.03232', '-0.4219', '-0.1223', '-0.6665', '0.2311', '0.3755', '-0.01252', '0.3782', '-0.396', '0.2357', '0.2137', '-0.06866', '-0.3857', '0.3293', '0.12366', '0.582', '-0.398', '0.4912', '0.7275', '0.7744', '-0.01467', '-0.7007', '0.5044', '0.0721', '0.621', '-0.0722', '0.0329', '0.687', '-0.0968', '-0.7886', '0.2484', '0.8623', '-0.1486', '-0.5757', '0.07025', '0.08716', '0.3574', '0.685', '0.4663', '0.6714', '0.157', '0.11926', '1.06', '0.4202', '0.4644', '0.331', '0.08734', '-0.02249']",,,C536370,759.89,,,
mondo:0008796,aniridia-renal agenesis-psychomotor retardation syndrome,"['Sommer-Rathbun-Battles syndrome', 'aniridia renal agenesis psychomotor retardation', 'aniridia, partial, with unilateral renal agenesis and psychomotor retardation', 'Sommer Rathbun Battles syndrome', 'aniridia partial with unilateral renal agenesis and psychomotor retardation']",,206750,1064,C1859782,,,,C000598722,,,,
mondo:0008797,anodontia,"['developmental absence of tooth', 'teeth, permanent, absence of', 'anodontia of permanent dentition', 'absence of permanent teeth', 'total anodontia of permanent and deciduous teeth', 'complete absence of teeth']",13714,206780,99797,,,,,D000848,520.0,K00.0,10002583,
mondo:0008798,nonsyndromic congenital nail disorder 4,"['RSPO4 isolated congenital anonychia', 'isolated congenital anonychia caused by mutation in RSPO4', 'nail disorder, nonsyndromic congenital, type 4', 'anonychia congenita', 'NDNC4', 'anonychia/hyponychia congenita', 'nonsyndromic congenital nail disorder type 4', 'nail disorder, nonsyndromic congenital, 4', 'HYPONYCHIA congenita', 'anonychia congenita totalis', 'anonychia totalis']",0080082,206800,94150,,"['-0.284', '0.1571', '-0.002254', '-0.0932', '0.1549', '-0.2292', '-0.06207', '0.01576', '-0.282', '-0.2418', '-0.098', '-0.0371', '-0.1519', '0.02525', '0.07056', '-0.02289', '0.041', '-0.0898', '-0.1373', '-0.3442', '-0.01266', '0.00212', '0.1606', '-0.06024', '0.1642', '0.11255', '-0.04968', '0.0355', '0.1223', '-0.1655', '0.156', '0.00996', '0.0801', '0.08167', '0.1809', '-0.112', '0.02942', '-0.09076', '0.0716', '-0.1519', '-0.05286', '-0.1605', '0.11975', '-0.08716', '-0.1027', '-0.2484', '0.03552', '0.1304', '0.127', '-0.0336', '0.004375', '-0.1172', '0.04135', '0.01497', '-0.3008', '-0.2161', '0.3774', '0.06586', '-0.2405', '0.0538', '0.1089', '0.0648', '0.0717', '-0.005463', '0.07227', '0.11993', '0.1798', '0.0762', '-0.2162', '0.1295', '-0.2822', '0.02135', '0.0939', '-0.1886', '0.08374', '0.01179', '0.08813', '-0.003792', '-0.1444', '-0.0841', '-0.06042', '0.02498', '0.0369', '0.0587', '0.0402', '-0.2039', '0.06', '0.3086', '0.10223', '0.11237', '-0.04105', '0.04398', '0.09125', '-0.09247', '0.447', '-0.003366', '0.2686', '-0.3625', '0.09125', '0.003145']",,,C536377,,,,
mondo:0008799,anophthalmia/microphthalmia-esophageal atresia syndrome,"['Aeg syndrome', 'anophthalmia clinical with associated anomalies', 'microphthalmia and esophageal atresia syndrome', 'microphthalmia, syndromic 3', 'SOX2 anophthalmia syndrome', 'SOX2-related eye disorders', 'MCOPS3', 'optic nerve hypoplasia and abnormalities of the central nervous system', 'syndromic microphthalmia, type 3', 'microphthalmia, syndromic type 3', 'syndromic microphthalmia type 3', 'anophthalmia microphthalmia esophageal atresia', 'anophthalmia, clinical, with associated anomalies', 'anophthalmia-esophageal-genital syndrome', 'anophthalmia esophageal genital syndrome']",0111801,206900,77298,,"['-0.0964', '-0.3645', '0.1682', '-0.2688', '0.3816', '-0.2737', '0.517', '0.604', '-0.1819', '-0.8164', '-0.1722', '-0.767', '-0.572', '-0.1311', '-0.497', '-0.2507', '0.4165', '-0.4065', '-0.4675', '-0.9023', '0.3032', '0.1101', '-0.03464', '-0.3616', '0.1921', '-0.2455', '-0.512', '0.12134', '0.643', '-0.2805', '0.3196', '-0.1157', '0.2605', '-0.106', '0.1456', '-0.1942', '-0.3362', '-0.548', '-0.414', '0.2496', '0.3804', '0.06116', '0.0843', '-0.512', '0.0602', '-0.2013', '0.1804', '-0.16', '-0.432', '0.0745', '-0.07874', '0.0935', '-0.02676', '0.05396', '-0.333', '-0.07666', '0.09534', '-0.1586', '-0.3713', '0.3958', '0.331', '0.03464', '0.1394', '0.07214', '-0.3938', '-0.05585', '0.03195', '0.6963', '-0.8237', '0.0686', '-0.6143', '0.4243', '0.2483', '0.1818', '0.322', '-0.2036', '0.0708', '-0.0487', '-0.399', '0.02321', '0.07367', '0.459', '0.3044', '0.666', '-0.1603', '-0.2328', '0.2788', '0.126', '-0.2471', '-0.325', '0.3203', '0.512', '0.3845', '-0.1785', '0.6978', '-0.005733', '0.3848', '-0.687', '0.281', '0.2284']",,,,758.5,,,
mondo:0008800,microphthalmia with limb anomalies,"['MLA', 'Waardenburg anophthalmia syndrome', 'ophthalmoacromelic syndrome', 'microphthalmia with limb anomalies', 'Ophthalmoacromelic syndrome', 'anophthalmos-syndactyly', 'anophthalmia-syndactyly syndrome', 'anophthalmos with limb anomalies', 'anophthalmia Waardenburg syndrome', 'anophthalmia-syndactyly', 'OAS']",0060861,206920,1106,,"['0.5244', '-0.5347', '-0.0896', '-0.1593', '-0.05038', '-0.01312', '0.10004', '0.8657', '-0.576', '-1.041', '-0.04202', '-0.4136', '-0.1155', '0.4536', '-0.507', '-0.3987', '0.528', '-0.4949', '0.04788', '-1.156', '0.167', '-0.07855', '0.309', '-0.483', '0.0711', '0.1847', '-0.656', '0.2603', '0.6016', '0.285', '0.07294', '-0.2903', '-0.2896', '0.0763', '-0.01014', '-0.2084', '0.4114', '-1.05', '-0.11884', '0.2319', '0.352', '-0.2197', '0.3376', '-0.4517', '0.5117', '-0.1112', '-0.2177', '0.09143', '-0.1191', '0.10925', '-0.1898', '-0.488', '0.2247', '-0.0873', '-0.284', '-0.4685', '-0.2406', '-0.221', '-0.1685', '0.07886', '0.1598', '-0.34', '0.01685', '0.2864', '-0.512', '0.1678', '0.4128', '0.3171', '-0.425', '0.1606', '-0.3396', '0.183', '-0.006016', '-0.0886', '0.3828', '0.1996', '0.2874', '-0.4595', '-0.3022', '-0.2292', '0.2288', '0.2642', '0.3008', '1.146', '-0.6333', '0.6567', '-0.4475', '-0.12415', '0.3755', '0.04837', '-0.01573', '0.4866', '0.05917', '0.2568', '0.1816', '-0.165', '-0.1855', '-0.6177', '0.842', '-0.1466']",,,C537769,755.8,,,
mondo:0008801,anosmia for isobutyric acid,['anosmia for isobutyric acid'],,207000,,,,,,,,,,
mondo:0008802,"antithrombin, familial hemorrhagic diathesis due to","['antithrombin, familial hemorrhagic diathesis due to']",,207300,,C1859761,,,,C565947,,,,
mondo:0008803,Antley-Bixler syndrome,"['trapezoidocephaly-synostosis syndrome', 'osteodysgenesis, multisynostotic with fractures', 'osteodysgenesis, multisynostotic, with fractures', 'Antley Bixler syndrome', 'trapezoidocephaly synostosis syndrome', 'multisynostotic osteodysgenesis with long bone fractures']",0081289,,83,,"['0.0665', '-0.11725', '-0.00814', '-0.593', '0.334', '-0.3179', '0.3308', '0.9644', '-0.5376', '-0.3547', '0.1353', '-0.5693', '-0.3525', '0.2944', '-0.1771', '0.2336', '0.1678', '-0.11426', '-0.2249', '-0.9844', '-0.08386', '0.03522', '0.7954', '-0.11237', '0.214', '0.3481', '0.0725', '-0.3733', '0.913', '-0.552', '0.2144', '-0.6025', '0.075', '0.3047', '0.03766', '-0.52', '0.202', '-0.331', '-0.41', '-0.4583', '0.1842', '-0.0941', '0.3997', '-0.5083', '0.7485', '-0.4414', '-0.1217', '0.4263', '0.01127', '-0.1558', '-0.2198', '-0.4421', '0.4038', '-0.04718', '-0.405', '-0.3342', '-0.213', '0.3892', '0.404', '0.2847', '0.1475', '0.1732', '-0.6924', '-0.2374', '-0.09375', '-0.2554', '0.1273', '0.28', '-0.5474', '0.2822', '-0.399', '0.132', '0.31', '0.0987', '-0.4927', '0.29', '0.1832', '-0.275', '-0.1543', '0.3535', '0.04202', '0.8633', '-0.1508', '0.612', '-0.4207', '0.0818', '0.319', '0.1642', '-0.1909', '-0.4536', '-0.2086', '0.611', '-0.6294', '-0.1299', '0.3574', '0.4788', '0.6885', '-0.4304', '0.35', '-0.342']",,,,,,,
mondo:0008806,Aphalangy-hemivertebrae-urogenital-intestinal dysgenesis syndrome,"['Johnson Munson syndrome', 'Aphalangy of the hands and feet, hemivertebrae, and visceral malformations', 'APHALANGY with hemivertebrae', 'Johnson-Munson syndrome']",,207620,1112,C1859754,,,,C535881,,,,
mondo:0008807,"apnea, central sleep","['sleep apnea, lethal central', 'apnea, central sleep']",,207720,,C0520680,,,,,,,,
mondo:0008808,aplasia cutis congenita-intestinal lymphangiectasia syndrome,"['ACC with intestinal lymphangiectasia', 'aplasia cutis congenita intestinal lymphangiectasia', 'aplasia cutis congenita with intestinal lymphangiectasia', 'Bronspiegel-Zelnick syndrome', 'autosomal recessive aplasia cutis']",,207731,1116,,,,,C537788,,,,
mondo:0008809,polyneuropathy-hand defect syndrome,"['Hamanishi-Ueba-Tsuji syndrome', 'congenital aplasia of the extensor muscles of the fingers and thumb associated with generalised polyneuropathy', 'congenital aplasia of the extensor muscles of the fingers and thumb associated with generalized polyneuropathy', 'polyneuropathy, hand defect', 'Hamanishi Ueba Tsuji syndrome', 'aplasia of extensor muscles of fingers, unilateral, with generalised polyneuropathy', 'aplasia of extensor muscles of fingers, unilateral, with generalized polyneuropathy', 'digital extensor muscle aplasia-polyneuropathy']",,207740,2926,C2930955,,,,C535624,,,,
mondo:0008810,familial apolipoprotein C-II deficiency,"['C-II Anapolipoproteinemia', 'hyperlipoproteinemia, type IB', 'hyperlipoproteinemia, type 1B', 'apolipoprotein C-II deficiency', 'Apoc2 deficiency', 'familial apoC-II deficiency']",0111418,207750,309020,C1720779,"['-0.1532', '0.191', '-0.006416', '-0.0241', '0.2225', '-0.194', '-0.2084', '0.1376', '-0.0946', '-0.0646', '-0.04773', '0.00109', '0.11926', '-0.2047', '-0.0669', '-0.1794', '0.1855', '0.05804', '-0.1936', '-0.3552', '0.08685', '-0.2362', '0.2283', '0.05136', '0.08624', '0.1294', '0.1965', '-0.1309', '-0.09216', '-0.254', '0.2479', '0.0378', '0.2825', '0.0387', '-0.04236', '-0.2251', '0.05188', '0.02275', '0.0434', '-0.5522', '0.05896', '-0.2491', '0.1683', '-0.2295', '-0.3108', '-0.3625', '0.2383', '0.2384', '0.2585', '0.05005', '-0.05807', '-0.1249', '0.0439', '-0.05505', '-0.1765', '-0.08203', '0.248', '-0.03397', '-0.3892', '0.09955', '0.00535', '0.1842', '0.3281', '-0.2664', '0.1342', '0.038', '0.0828', '0.1364', '-0.3838', '0.02847', '-0.1982', '-0.1008', '-0.000888', '0.2383', '0.1051', '0.2201', '0.0217', '0.29', '-0.2019', '-0.09076', '0.0627', '0.03114', '-0.10187', '0.0648', '0.02225', '0.02042', '0.10956', '0.1566', '0.3054', '0.04105', '0.01938', '0.0992', '-0.2218', '-0.1759', '0.43', '0.4258', '0.159', '-0.4368', '-0.3484', '0.04868']",,,,,,,
mondo:0008811,XK aprosencephaly,"['XK-aprosencephaly syndrome', 'Xk syndrome', 'atelencephaly', 'XK-aprosencephaly', 'aprosencephaly-atelencephaly syndrome', 'aprosencephaly syndrome', 'Garcia-Lurie syndrome', 'XK aprosencephaly syndrome']",,207770,3469,C0795952,,,,C536767,,,,
mondo:0008812,AREDYLD syndrome,"['acral renal ectodermal dysplasia lipoatrophic diabetes', 'acrorenal Field defect, ectodermal dysplasia, and lipoatrophic diabetes', 'AREDYLD', 'acrorenal defect-ectodermal dysplasia-diabetes syndrome']",,207780,1133,C0342280,,,,C537427,753.3,,,
mondo:0008813,arachnoid cyst,['arachnoid cysts'],,,2356,C0078981,,C3455,,D016080,,,10049005,
mondo:0008814,hyperargininemia,"['argininemia', 'deficiency of canavanase', 'Arg1 deficiency', 'hyperargininemia', 'arginase deficiency']",9278,207800,90,C0268548,"['0.277', '0.3787', '-0.06586', '0.3123', '0.3403', '-0.605', '0.1423', '0.2551', '-0.1353', '0.1648', '-0.4631', '-0.1025', '0.2012', '0.296', '0.01054', '-0.2332', '0.11664', '0.359', '-0.1918', '-0.646', '0.03003', '-0.3494', '0.3704', '-0.3682', '0.181', '0.011765', '0.1139', '0.1588', '-0.1528', '-0.306', '0.564', '0.3071', '0.3215', '0.64', '-0.6216', '-0.1238', '-0.002924', '-0.04932', '-0.5967', '-0.02698', '-0.02135', '-0.7886', '0.0691', '0.1724', '-0.263', '-0.2869', '0.0611', '-0.1924', '0.2522', '0.7646', '-0.1931', '0.05154', '-0.298', '-0.5806', '0.2864', '-0.252', '0.03867', '0.155', '-0.2407', '-0.10876', '-0.0549', '0.1631', '0.585', '-0.4277', '-0.409', '0.2668', '0.1687', '0.2408', '-0.511', '-0.0272', '0.2595', '0.148', '-0.173', '-0.3796', '0.5806', '-0.002314', '0.3474', '-0.10065', '-0.3643', '-0.2147', '0.2524', '-0.05435', '-0.2175', '0.1443', '0.432', '0.1765', '0.2808', '0.04425', '0.3772', '-0.0322', '0.0781', '0.598', '-0.354', '-0.235', '0.1853', '0.548', '0.371', '-0.11334', '0.1636', '0.1361']",C84568,,D020162,,,10062695,
mondo:0008815,argininosuccinic aciduria,"['argininosuccinic acid lyase deficiency', 'ASA deficiency', 'argininosuccinase deficiency', 'arginosuccinase deficiency', 'argininosuccinatelyase deficiency', 'ASL deficiency', 'deficiency of argininosuccinate lyase', 'inborn error of urea synthesis, arginino succinic type', 'argininosuccinicaciduria', 'argininosuccinate lyase deficiency', 'arginino succinase deficiency', 'urea cycle disorder, arginino succinase type', 'argininosuccinate acidemia', 'argininosuccinic acidemia', 'argininosuccinic aciduria']",14755,207900,23,C0268547,"['-0.04102', '-0.2986', '-0.1256', '0.0765', '0.04642', '-0.4949', '-0.03012', '0.81', '-0.8623', '0.2152', '-0.5796', '-0.547', '0.2876', '0.2384', '-0.5405', '-0.283', '0.1671', '-0.1301', '0.2844', '-1.134', '0.1713', '-0.2435', '0.807', '-0.4495', '0.03723', '-0.2727', '-0.2194', '-0.4438', '0.003048', '-0.286', '0.3809', '0.2935', '0.2072', '0.4326', '-0.58', '-0.0711', '-0.4912', '0.05115', '0.366', '-0.0961', '0.734', '-0.1606', '0.6577', '0.227', '-0.2495', '-0.007595', '-0.4492', '-0.193', '-0.1572', '1.021', '-0.4016', '0.0686', '0.2498', '-0.342', '0.4463', '0.4675', '0.6313', '-0.4346', '-0.2152', '0.2869', '0.3416', '0.275', '0.7275', '-0.2651', '-0.2786', '0.3096', '0.458', '0.2742', '-0.414', '0.417', '-0.2021', '0.26', '-0.3914', '-0.03687', '0.2896', '0.03842', '0.509', '-0.3901', '-0.3901', '-0.2289', '0.0117', '-0.207', '-0.4607', '-0.852', '0.663', '0.8706', '0.1263', '0.3298', '0.2754', '0.1353', '0.2622', '0.2952', '0.1488', '-0.2605', '0.05188', '0.4797', '0.06128', '-0.01365', '-0.02185', '-0.1426']",C84569,,D056807,,,10058299,
mondo:0008816,Chiari malformation type II,"['Chiari malformation type 2', 'Arnold-Chiari malformation type 2', 'Chiari type II malformation', 'Cm2', 'Arnold-Chiari malformation', 'Chiari malformation type II', 'Arnold-Chiari malformation type II', 'Arnold Chiari malformation type II']",,207950,1136,,,,,,,,10056945,
mondo:0008817,"arterial calcification, generalized, of infancy, 1","['arterial calcification, generalized, of infancy, 1', 'generalized arterial calcification of infancy 1', 'arterial calcification of infancy caused by mutation in ENPP1', 'GACI1', 'idiopathic infantile arterial calcification', 'generalised arterial calcification of infancy 1', 'Gaci', 'arteriopathy, occlusive infantile', 'arterial calcification, idiopathic infantile', 'ENPP1 arterial calcification of infancy', 'arterial calcification, generalized, of infancy, type 1', 'coronary sclerosis, medial, of infancy']",,208000,,,,C128805,,,,,,
mondo:0008818,arterial tortuosity syndrome,"['ATS', 'arterial tortuosity', 'arterial tortuosity syndrome']",0050645,208050,3342,C1859726,"['-0.1888', '-0.0889', '-0.74', '-0.508', '0.587', '-0.5205', '0.4602', '0.724', '-0.5757', '-0.1399', '-0.6104', '-0.05154', '0.6094', '0.2852', '-0.4412', '0.394', '0.2764', '0.1583', '0.2095', '-0.2122', '0.1451', '0.2087', '0.3984', '-0.1757', '-0.2179', '0.0465', '0.1517', '0.547', '0.765', '-0.356', '0.68', '0.3486', '0.627', '-0.1705', '-0.01048', '-0.1772', '-0.04904', '-0.2405', '0.2394', '-0.8647', '0.3577', '-0.266', '0.4773', '0.0649', '0.3677', '0.1388', '-0.132', '0.629', '-0.2206', '-0.601', '-0.02226', '0.3408', '0.5254', '0.4795', '-0.0758', '-0.525', '0.1539', '0.4827', '-0.1589', '-0.05945', '0.1503', '0.567', '-0.4124', '0.0681', '0.2452', '-0.001552', '0.2266', '0.4333', '-0.3457', '0.4434', '-0.4688', '-0.136', '-0.1387', '0.2285', '-0.212', '0.1064', '0.3918', '0.02263', '-0.0364', '-0.3152', '0.1687', '-0.09894', '-0.12134', '0.5776', '-0.2173', '0.5244', '0.233', '0.01385', '-0.1241', '-0.4187', '0.433', '0.489', '-0.319', '0.4868', '0.7964', '-0.1548', '0.972', '0.01309', '-0.1533', '0.0954']",,,C565942,,Q87.82,,
mondo:0008819,"arteriosclerosis, severe juvenile","['arteriosclerosis, severe juvenile']",,208060,,C1859725,,,,C565941,,,,
mondo:0008821,"arthrogryposis, distal, with intellectual disability and characteristic facies","['arthrogryposis, distal, with mental retardation and characteristic facies', 'arthrogryposis, distal, with intellectual disability and characteristic facies']",,208081,,C1859723,,,,C565940,,,,
mondo:0008822,"arthrogryposis, renal dysfunction, and cholestasis 1","['arthrogryposis, renal dysfunction, and cholestasis type 1', 'Arc syndrome', 'ARCS1', 'arthrogryposis, renal dysfunction, and cholestasis 1', 'arthrogryposis-renal dysfunction-cholestasis syndrome caused by mutation in VPS33B', 'VPS33B arthrogryposis-renal dysfunction-cholestasis syndrome']",0111353,208085,,,,,,,,,,
mondo:0008823,"arthrogryposis multiplex congenita 2, neurogenic type","['AMCN', 'arthrogryposis multiplex congenita neurogenic type', 'neurogenic arthrogryposis multiplex congenita', 'AMC neurogenic type', 'arthrogryposis multiplex congenita, neurogenic type', 'neurogenic type of AMC', 'AMC, neurogenic type']",0090124,208100,1143,C1859721,"['-0.6646', '0.2283', '0.0892', '-0.209', '-0.02731', '-0.4639', '0.0611', '0.1741', '-0.5723', '-0.1359', '-0.00241', '0.06024', '-0.1967', '-0.03296', '0.0498', '0.1542', '0.1566', '0.010124', '0.0174', '-0.8276', '-0.03555', '-0.179', '0.2261', '0.10535', '-0.00712', '0.08417', '0.1642', '-0.1052', '-0.001945', '-0.05472', '-0.03223', '0.05762', '0.3198', '0.1261', '0.145', '-0.1841', '-0.07086', '-0.00486', '-0.05435', '-0.1439', '-0.249', '-0.584', '0.0316', '0.324', '0.01385', '-0.0977', '-0.07996', '0.2472', '0.2125', '0.11115', '-0.12146', '0.1737', '0.08704', '-0.1722', '-0.276', '-0.514', '0.1159', '-0.262', '-0.01686', '-0.126', '0.387', '-0.1365', '-0.1432', '0.00878', '-0.1815', '-0.02666', '0.4163', '0.3208', '-0.3616', '-0.03973', '-0.4385', '0.01602', '0.1804', '-0.2034', '-0.001312', '0.0558', '-0.04633', '0.125', '-0.3867', '-0.22', '0.1891', '0.2576', '-0.0842', '0.413', '-0.09204', '0.2157', '-0.1576', '-0.01913', '0.1831', '-0.1267', '0.1376', '0.03827', '0.2556', '0.1931', '0.3086', '0.1418', '0.4512', '-0.2017', '0.1653', '0.2299']",,,C536614,,,,
mondo:0008824,fetal akinesia deformation sequence,"['fetal akinesia deformation sequence', 'arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome', 'foetal akinesia sequence', 'fetal akinesia sequence', 'arthrogryposis multiplex congenita with pulmonary hypoplasia', 'FADS']",0111375,,,,,C129071,,C536647,754.89,,,
mondo:0008825,arthrogryposis multiplex congenita-whistling face syndrome,"['arthrogryposis multiplex congenita whistling face', 'ILLUM syndrome', 'arthrogryposis, whistling face, and developintellectual disability', 'arthrogryposis, whistling face, and developmental retardation', 'lethal autosomal recessive arthrogryposis multiplex congenita with whistling face and calcifications of the nervous system', 'Illum syndrome']",,208155,1150,C1859711,,,,C538401,,,,
mondo:0008826,"arthrogryposis-hyperkeratosis syndrome, lethal form","['Johnston Aarons Schelley syndrome', 'Joint contractures, hyperkeratosis, and severe hypoplasia of the posterior columns', 'Johnston-Aarons-Schelley syndrome', 'arthrogryposis with hyperkeratosis']",,208158,1485,C1859710,,,,C535883,,,,
mondo:0008827,progressive pseudorheumatoid arthropathy of childhood,"['SEDT-PA', 'progressive pseudorheumatoid arthropathy of childhood', 'PPAC', 'progressive pseudorheumatoid dysplasia', 'spondyloepiphyseal dysplasia tarda - progressive arthropathy', 'PPD', 'progressive pseudorheumatoid chondrodysplasia', 'spondyloepiphyseal dysplasia tarda with progressive arthropathy', 'arthropathy, progressive pseudorheumatoid, of childhood', 'spondyloepiphyseal dysplasia tarda-progressive arthropathy syndrome']",0090004,208230,1159,,"['-0.3376', '0.11444', '-0.03693', '0.01727', '-0.0479', '-0.9497', '0.04086', '1.083', '-0.381', '-0.03592', '-0.1711', '0.3389', '-0.3274', '0.63', '0.2666', '0.1422', '-0.0705', '-0.0839', '-0.1357', '-0.4458', '-0.1741', '-0.4531', '0.505', '-0.2151', '-0.0333', '0.2208', '0.3098', '0.10913', '-0.3025', '0.2094', '0.3313', '-0.277', '-0.2426', '0.2156', '0.227', '-0.7812', '-0.5083', '-0.33', '0.571', '0.1798', '-0.3691', '-0.4666', '0.0617', '-0.11615', '0.2023', '0.00861', '-0.299', '0.126', '-0.4077', '-0.2374', '0.302', '0.1672', '0.3506', '-0.09', '0.2527', '-0.5117', '-0.21', '-0.4968', '-0.1758', '-0.1054', '0.3623', '0.1295', '-0.5317', '0.009476', '-0.2725', '0.0405', '0.3584', '0.0773', '0.2443', '0.3784', '-0.624', '-0.3962', '0.0848', '-0.3198', '0.2239', '0.5693', '-0.5015', '0.2338', '-0.0751', '-0.662', '0.1305', '-0.07965', '-0.2225', '0.3767', '-0.2957', '0.4377', '0.1608', '0.1565', '0.0827', '-0.10065', '-0.1907', '-0.01098', '0.05115', '-0.3933', '0.487', '0.02031', '0.864', '-0.3384', '0.00811', '-0.3901']",,,C535387,756.9,,,
mondo:0008828,camptodactyly-arthropathy-coxa vara-pericarditis syndrome,"['congenital familial hypertrophic synovitis', 'camptodactyly-arthropathy-coxa vara-pericarditis syndrome', 'hypertrophic synovitis, congenital familial', 'pericarditis arthropathy camptodactyly syndrome', 'camptodactyly arthropathy pericarditis syndrome', 'CACP syndrome', 'pericarditis-arthropathy-camptodactyly syndrome', 'CACP', 'PAC syndrome', 'familial fibrosing serositis', 'arthropathy camptodactyly syndrome', 'fibrosing serositis, familial', 'camptodactyly-arthropathy-coxa-vara-pericarditis syndrome', 'Jacobs syndrome', 'arthropathy-camptodactyly syndrome', 'camptodactyly arthropathy coxa vara pericarditis syndrome', 'camptodactyly-arthropathy-pericarditis syndrome']",0090127,208250,2848,,"['0.03976', '-0.3804', '-0.362', '0.6543', '0.4082', '-0.2507', '0.426', '0.52', '-0.687', '-0.1434', '0.1192', '0.1333', '-0.04236', '0.4817', '-0.4805', '-0.1426', '-0.4812', '0.0972', '0.03867', '-0.8223', '0.3784', '0.9375', '-0.09814', '-0.74', '0.0278', '-0.282', '0.1295', '0.3167', '0.4531', '0.1678', '0.3467', '0.2688', '0.239', '0.10535', '0.1515', '-0.08264', '-0.839', '0.1768', '0.4175', '-0.1478', '-0.515', '-0.3616', '-0.0942', '0.0754', '0.964', '0.2908', '-0.775', '0.3481', '-0.0541', '0.08026', '0.1086', '0.256', '0.6377', '0.2131', '-0.4019', '-0.2012', '-0.4524', '-0.004543', '-0.1648', '-0.1484', '0.2095', '0.5376', '-0.29', '-0.09784', '-0.5117', '0.0616', '0.4583', '0.589', '-0.1338', '0.3816', '-0.758', '0.0763', '0.3826', '-0.6885', '-0.508', '-0.10956', '0.22', '1.199', '0.122', '0.12384', '-0.2054', '0.1926', '-0.10645', '-0.0409', '0.4104', '0.3909', '0.658', '0.7314', '0.4492', '0.1908', '-0.2354', '-0.1501', '-0.4253', '0.1876', '0.5356', '0.2937', '0.1492', '-0.3987', '0.06012', '-0.1465']",,0009028,C537560,,,,
mondo:0008829,chylous ascites,"['congenital chylous ascites', 'ascites, chylous']",,208300,1160,C0008732,,C34482,,D002915,457.8,,10003446,
mondo:0008830,aspartylglucosaminuria,"['Aspartylglucosamidase (AGA) deficiency', 'aspartylglucosaminidase deficiency', 'aspartylglycosaminuria', 'Glycoasparaginase', 'aspartylglucosaminuria', 'glycosylasparaginase deficiency', 'AGU', 'Aga deficiency']",0050461,208400,93,C0268225,"['-0.2576', '0.566', '-0.05652', '-0.3962', '0.01624', '-0.608', '-0.4355', '0.4077', '-0.4592', '-0.03156', '-0.1932', '-0.1553', '0.00115', '0.04175', '-0.0539', '0.2517', '-0.592', '-0.04004', '-0.4783', '-0.1516', '0.0358', '-0.0864', '0.4067', '-0.0558', '-0.2656', '-0.1888', '-0.285', '-0.2852', '-0.4736', '-0.1879', '0.0689', '0.2412', '0.09735', '0.142', '0.1432', '-0.3167', '-0.0913', '-0.6157', '-0.1034', '-0.2258', '-0.1272', '-0.862', '0.04672', '0.3025', '-0.2637', '-0.2245', '0.3164', '0.03647', '0.1345', '-0.16', '0.6177', '-0.1522', '0.00651', '0.4004', '0.3987', '-0.826', '0.3962', '-0.1659', '-0.2029', '-0.1131', '0.09546', '-0.1818', '-0.1212', '-0.1421', '0.06', '-0.3123', '0.571', '-0.0409', '-0.2585', '0.1948', '-0.5312', '-0.02962', '-0.243', '0.2234', '0.4614', '0.4475', '-0.3855', '0.167', '-0.498', '0.01608', '-0.3174', '-0.1598', '0.0888', '0.4534', '0.08795', '-7.945e-05', '0.1153', '0.1224', '0.2964', '-0.02216', '0.4075', '0.2922', '-0.1603', '-0.1387', '0.4883', '0.3254', '-0.2322', '-0.3606', '0.5366', '-0.271']",C61273,,D054880,,,10068220,
mondo:0008831,asphyxiating thoracic dystrophy 1,"['ATD1', 'short-rib thoracic dysplasia 1 with or without polydactyly', 'asphyxiating thoracic dystrophy type 1', 'thoracic-pelvic-phalangeal dystrophy', 'SRTD1', 'asphyxiating thoracic dystrophy 1', 'Jeune syndrome']",0110085,208500,,CN119532,,,,,,,,
mondo:0008832,right atrial isomerism,"['right atrial isomerism (disease)', 'splenic agenesis syndrome', 'bilateral right-sidedness sequence', 'Ivemark syndrome', 'polysplenia syndrome', 'Polyasplenia', 'RAI', 'asplenia with cardiovascular anomalies', 'right isomerism', 'asplenia syndrome', 'Vah, autosomal recessive', 'right atrial isomerism', 'heterotaxy, Visceroatrial, autosomal recessive', 'right atrial isomerism (ivemark)']",0060856,208530,97548,,"['-0.4482', '-0.3484', '0.279', '-0.1808', '0.643', '-0.157', '0.10406', '0.2377', '-0.633', '-0.241', '-0.6504', '-0.699', '0.126', '0.3638', '-0.5654', '-0.0943', '-0.3398', '-0.1324', '-0.2734', '-0.5166', '0.02217', '0.4663', '0.788', '-0.1467', '0.395', '-0.2527', '0.0564', '0.579', '0.3213', '0.2534', '0.744', '0.1993', '0.4238', '0.27', '0.10223', '-0.513', '-0.10516', '0.2817', '0.0825', '-0.4717', '-0.01936', '0.1261', '0.3171', '0.2764', '-0.1069', '0.1004', '-0.2461', '0.3718', '-0.2573', '0.324', '-0.1293', '-0.1359', '0.01758', '0.0871', '-0.4963', '-0.1184', '0.3237', '0.3264', '-0.09393', '0.1312', '0.03394', '0.4126', '0.2769', '0.2678', '-0.2458', '-0.3823', '0.601', '0.623', '-0.1648', '0.3223', '-0.3328', '0.3696', '0.1649', '0.05023', '-0.325', '-0.1653', '0.0946', '0.3015', '-0.4175', '-0.3628', '-0.0509', '0.0199', '-0.02354', '0.09485', '-0.2213', '-0.479', '0.3042', '0.2764', '-0.4055', '-0.3328', '-0.2095', '-0.2168', '-0.01875', '-0.2126', '1.145', '-0.1179', '0.4592', '-0.453', '-0.0702', '0.1794']",,,,,,10068335,0011536
mondo:0008833,renal-hepatic-pancreatic dysplasia 1,"['renal-hepatic-pancreatic dysplasia caused by mutation in NPHP3', 'renal-hepatic-pancreatic dysplasia type 1', 'renal-hepatic-pancreatic dysplasia 1', 'Rhpd', 'RHPD1', 'NPHP3 renal-hepatic-pancreatic dysplasia']",,208540,,C3715199,,,,,,,,
mondo:0008834,"asthma, nasal polyps, and aspirin intolerance","['Asa triad', 'asthma, nasal polyps, and aspirin intolerance', 'asthma, aspirin-induced, susceptibility to', 'asthma and nasal polyps']",0111579,208550,,C1859648,,,,,,,,
mondo:0008835,"asthma, short stature, and elevated IgA","['asthma, short stature, and elevated IgA']",,208600,,C1859647,,,,C565934,,,,
mondo:0008836,ataxia with myoclonic epilepsy and presenile dementia,['ataxia with myoclonic epilepsy and presenile dementia'],,208700,,C1859646,,,,C565933,,,,
mondo:0008837,"ataxia, deafness, and cardiomyopathy","['ataxia, deafness, and cardiomyopathy']",,208750,,C1859645,,,,C565932,,,,
mondo:0008838,ataxia - deafness - intellectual disability syndrome,"['ataxia-hearing loss-intellectual disability syndrome', 'Reardon-Baraitser syndrome', 'Reardon Wilson Cavanagh syndrome', 'familial ataxia, deafness, and developmental delay', 'ataxia-deafness-retardation syndrome', 'ataxia, hearing loss, and intellectual disability', 'Adr syndrome', 'ataxia, hearing loss, and mental retardation']",,208850,1188,,,,,C535295,,,,
mondo:0008839,ataxia-microcephaly-cataract syndrome,"['ataxia-microcephaly-cataract syndrome', 'AMC syndrome']",,208870,,C0796056,,,,C563086,,,,
mondo:0008840,ataxia telangiectasia,"['Louis Bar syndrome', 'ataxia - telangiectasia', 'cerebello-oculocutaneous telangiectasia', 'AT1', 'ataxia - telangiectasia variant', 'ataxia-telangiectasia', 'AT, complementation group C', 'AT, complementation group A', 'AT, complementation group D', 'Louis-Bar syndrome', 'AT, complementation group E', 'immunodeficiency with ataxia telangiectasia', 'boder-Sedgwick syndrome', 'AT', 'ataxia telangiectasia syndrome', 'ataxia telangiectasia']",12704,208900,100,C1876175,"['-0.044', '-0.1976', '-0.0638', '0.02357', '-0.0668', '-0.6196', '0.5205', '0.1475', '-0.6562', '-0.7334', '0.00732', '0.4258', '-0.1082', '0.11804', '0.638', '-0.3113', '-0.0844', '-0.4116', '0.267', '-0.879', '-0.132', '-0.2452', '0.2532', '-0.6914', '0.2172', '-0.5146', '-0.1595', '-0.06165', '-0.008514', '-0.9927', '0.07166', '0.4048', '-0.2937', '0.004272', '0.2465', '0.008705', '0.0727', '0.162', '0.4338', '0.484', '0.3623', '-0.03162', '-0.3167', '0.4275', '0.3918', '-0.64', '0.04205', '0.04834', '0.3972', '-0.0773', '-0.3533', '0.2203', '0.077', '-0.251', '-0.1073', '-0.4438', '0.1562', '0.3716', '-0.2678', '0.3926', '-0.6143', '0.3057', '-0.003937', '0.002222', '-0.31', '0.1945', '0.3203', '0.2876', '-0.5723', '0.2886', '0.554', '0.5894', '-0.1604', '-0.8936', '0.604', '0.2988', '0.1876', '0.22', '0.222', '0.5117', '-0.1821', '-0.7905', '0.2485', '0.6274', '-0.362', '-0.6753', '0.262', '-0.00947', '0.2913', '0.4624', '0.2273', '0.4458', '0.1797', '-0.1653', '0.783', '0.964', '0.4888', '0.2205', '-0.2915', '0.1736']",C2887,,D001260,334.8,,10003594,
mondo:0008841,ataxia-telangiectasia with generalized skin pigmentation and early death,['ataxia-telangiectasia with generalized skin pigmentation and early death'],,208910,,C1859615,,,,C565930,,,,
mondo:0008842,"ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia","['APTX oculomotor apraxia or related oculomotor disease', 'EAOH', 'ataxia-oculomotor apraxia 1', 'ataxia-oculomotor apraxia type 1', 'ataxia, early-onset, with oculomotor apraxia and hypoalbuminemia', 'cerebellar ataxia, early-onset, with hypoalbuminemia', 'ataxia-telangiectasia-like syndrome', 'EOCA-HA', 'early-onset ataxia with oculomotor apraxia and hypoalbuminemia', 'early-onset cerebellar ataxia with hypoalbuminemia', 'ataxia-oculomotor apraxia syndrome', 'oculomotor apraxia or related oculomotor disease caused by mutation in APTX', 'AOA1', 'ataxia with oculomotor apraxia type 1', 'ataxia, adult-onset, with oculomotor apraxia']",0050754,208920,1168,C1859598,"['0.03084', '0.0595', '-0.0463', '-0.10297', '-0.4045', '-0.6577', '0.4265', '0.593', '-0.808', '-0.901', '0.11566', '0.5293', '0.0637', '-0.00894', '0.58', '-0.3337', '-0.1211', '-0.5073', '0.4307', '-0.794', '0.011345', '-0.2156', '0.01941', '-0.3372', '0.5654', '-0.3381', '-0.283', '-0.05447', '-0.1599', '-0.823', '0.153', '0.6494', '-0.4583', '-0.2161', '0.2292', '-0.1353', '-0.2281', '0.1995', '0.1873', '0.3435', '0.5415', '0.08936', '-0.4841', '0.219', '0.641', '-0.496', '-0.0335', '0.4727', '0.081', '-0.006256', '-0.149', '0.262', '-0.1976', '-0.66', '0.178', '-0.7026', '0.5015', '0.23', '-0.05576', '0.3633', '-0.3318', '0.1919', '0.3494', '-0.238', '-0.51', '0.4587', '0.4814', '0.48', '-0.2336', '0.3955', '0.496', '0.4666', '-0.4224', '-0.532', '1.023', '0.1595', '0.04544', '-0.1382', '0.01903', '0.4714', '-0.1434', '-1.065', '0.482', '0.804', '-0.0698', '-0.4304', '0.02866', '0.02524', '0.2489', '0.2261', '0.4666', '0.371', '0.00928', '-0.4016', '1.088', '0.704', '0.3647', '0.2725', '-0.0978', '0.1787']",,,C538013,,,,
mondo:0008843,atherosclerosis-deafness-diabetes-epilepsy-nephropathy syndrome,"['Feigenbaum-Bergeron-Richardson syndrome', 'atherosclerosis, premature, with deafness, nephropathy, diabetes mellitus, photomyoclonus, and degenerative neurologic disease', 'premature atherosclerosis with photomyoclonic epilepsy, deafness, diabetes mellitus, nephropathy, and neurodegenerative disorder', 'Feigenbaum Bergeron Richardson syndrome']",,209010,1192,,,,,C565928,,,,
mondo:0008844,"Athrombia, essential","['Athrombia, essential']",,209050,,C1859595,,,,C565927,,,,
mondo:0008845,atonic-astatic syndrome of Foerster,['atonic-astatic syndrome of Foerster'],,209100,,C1859594,,,,C565926,,,,
mondo:0008846,atransferrinemia,"['congenital hypotransferrinemia', 'atransferrinemia', 'familial hypotransferrinemia', 'congenital atransferrinemia', 'transferrin serum level quantitative trait locus 1', 'hereditary atransferrinemia', 'hypotransferrinemia, familial']",0050649,209300,1195,C0521802,"['0.0406', '-0.3364', '-0.422', '-0.01656', '0.4514', '-0.5474', '-0.2157', '0.666', '0.1407', '0.1938', '-0.457', '0.2607', '0.11615', '0.195', '-0.3516', '-0.00542', '-0.3691', '-0.1901', '-0.4456', '-0.9473', '-0.11346', '-0.2573', '0.3972', '-0.3914', '0.2247', '-0.273', '-0.1216', '-0.1554', '0.3467', '0.1611', '0.3098', '0.2222', '0.0803', '-0.08856', '-0.3823', '-0.536', '-0.2695', '-0.4026', '0.3994', '0.2029', '0.0241', '0.2184', '0.587', '-0.1727', '-0.2983', '0.0704', '-0.1577', '-0.054', '-0.66', '-0.119', '-0.2861', '-0.10254', '0.4382', '0.2405', '0.3794', '-0.0759', '0.503', '-0.1971', '-0.4583', '0.403', '0.2427', '0.252', '-0.005707', '-1.091', '0.0907', '-0.4082', '0.4387', '0.4954', '-0.5654', '-0.2534', '-0.196', '0.0881', '-0.2367', '-0.4023', '0.2455', '-0.6416', '-0.09705', '-0.3013', '-0.458', '0.2827', '0.2118', '-0.2473', '-0.2024', '-0.2325', '0.2125', '-0.07574', '0.505', '0.237', '0.509', '-0.309', '0.3743', '0.566', '-0.1628', '-0.143', '0.926', '0.8535', '0.2051', '-0.0324', '0.2756', '-0.2598']",C125693,,C538259,,,,
mondo:0008847,atrichia with papular lesions,"['papular atrichia', 'APL', 'atrichia with papular lesions']",0060689,209500,86819,C1859592,"['-0.0725', '0.11523', '-0.178', '-0.07153', '0.4915', '-0.689', '-0.473', '0.2435', '-0.354', '-0.083', '-0.553', '0.02089', '0.2478', '0.3384', '-0.3564', '0.1406', '0.2568', '-0.2534', '0.005672', '-0.657', '-0.3455', '-0.1091', '0.6475', '-0.0621', '0.3313', '0.2505', '-0.3848', '0.00803', '-0.474', '0.131', '0.6074', '-0.1895', '0.02965', '-0.03784', '0.1842', '0.4033', '-0.2269', '0.12024', '-0.00432', '0.141', '0.1293', '-0.08167', '-0.12494', '0.02864', '0.02724', '-0.219', '-0.2316', '-0.05408', '0.1505', '0.0657', '-0.3403', '0.05', '0.252', '0.2251', '-0.778', '-0.2961', '0.3643', '-0.0627', '-0.2961', '-0.2637', '0.11804', '0.02534', '0.12274', '0.1876', '-0.425', '0.206', '0.3845', '0.546', '0.0841', '0.578', '0.2433', '-0.1282', '0.3328', '0.04025', '0.0686', '0.0625', '-0.142', '0.00488', '-0.2588', '-0.511', '-0.00681', '-0.36', '0.426', '-0.1641', '0.0661', '-0.465', '-0.2118', '0.2925', '0.1862', '0.509', '0.6045', '0.3535', '-0.176', '0.6274', '0.05246', '0.05865', '0.3733', '-0.559', '0.4001', '0.4727']",,,C565924,,,,
mondo:0008848,atrioventricular dissociation,"['atrioventricular dissociation', 'atrioventricular dissociation (disease)', 'A-V dissociation']",,209600,,,,,,D006327,426.89,,,0011709
mondo:0008849,atrophoderma vermiculata,"['Atrophodermia reticulata symmetrica faciei', 'ava', 'Atrophodermia vermiculata', 'folliculitis ulerythematosa', 'folliculitis ulerythematosa reticulata', 'atrophoderma vermiculata', 'honeycomb atrophy', 'Atrophodermia reticulata', 'atrophoderma vermiculatum', 'folliculitis ulerythematosa reticulate']",0080756,209700,79100,,,,,,701.8,,,
mondo:0008850,Cooper-Jabs syndrome,"['aural atresia, multiple congenital anomalies, and intellectual disability', 'aural atresia-multiple congenital anomalies-intellectual disability syndrome', 'aural atresia, multiple congenital anomalies, and mental retardation']",,209770,1488,,,,,C565923,,,,
mondo:0008853,Barber-Say syndrome,"['hypertrichosis-atrophic skin-ectropion-macrostomia syndrome', 'hypertrichosis, atrophic skin, ectropion, and macrostomia', 'Barber-Say syndrome', 'BARBER-SAY syndrome', 'BBRSAY', 'hypertrichosis atrophic skin ectropion macrostomia', 'Barber Say syndrome', 'Bss']",0060549,209885,1231,C1319466,"['-7.11e-05', '0.004402', '0.4343', '-0.3665', '0.3418', '-0.03488', '-0.1628', '0.4746', '-0.1897', '-0.11835', '-0.587', '-0.2988', '-0.1156', '-0.1552', '-0.1467', '0.4272', '0.6377', '-0.2874', '-0.4065', '-0.674', '-0.3062', '0.0918', '0.2041', '-0.1876', '0.556', '-0.1293', '-0.4282', '0.1343', '0.5737', '-0.2263', '0.321', '0.09143', '-0.08734', '0.4395', '0.2905', '0.001171', '-0.1821', '-0.12195', '-0.2915', '-0.5234', '0.1282', '-0.07184', '-0.2844', '-0.2732', '0.0771', '-0.1633', '-0.1514', '0.4148', '-0.385', '-0.011086', '-0.1242', '0.0705', '0.0347', '0.2214', '-0.653', '-0.4937', '0.055', '-0.253', '-0.1433', '-0.00894', '0.2573', '0.2272', '-0.3738', '-0.005642', '0.137', '-0.425', '0.491', '0.4841', '-0.2544', '0.4636', '-0.4578', '0.2382', '0.424', '-0.161', '-0.2346', '0.0003667', '0.2057', '-0.3647', '-0.0167', '-0.267', '0.3618', '0.0858', '0.04785', '0.3674', '-0.06195', '0.03586', '-0.3005', '0.4983', '0.3206', '0.3164', '0.2004', '0.847', '0.2482', '0.475', '0.6895', '0.1592', '0.2908', '-0.2737', '0.5166', '0.3723']",,,C537908,,,,
mondo:0008854,Bardet-Biedl syndrome 1,"['BBS1', 'Bardet-Biedl syndrome type 1', 'Bardet-Biedl syndrome 1, modifier of', 'Bardet-Biedl syndrome 1']",0110123,209900,,C3806174,"['-0.2734', '0.0892', '-0.01245', '0.02383', '0.2659', '-0.3564', '-0.1952', '0.2183', '-0.2493', '-0.09296', '-0.04517', '-0.04443', '0.1973', '-0.0732', '0.1821', '-0.05457', '-0.1187', '-0.1278', '-0.0611', '-0.2976', '0.1506', '-0.05084', '0.1371', '-0.03882', '0.1654', '0.00873', '-0.1333', '0.0541', '0.05643', '-0.06946', '0.2625', '0.1227', '0.1427', '0.01449', '0.1523', '-0.1584', '-0.05356', '-0.1444', '0.06647', '-0.2289', '0.1807', '-0.2347', '0.04257', '-0.0493', '-0.0686', '-0.202', '-0.011856', '0.06274', '0.1531', '-0.1217', '-0.09546', '-0.06323', '-0.00804', '0.1809', '-0.09015', '-0.2167', '0.3936', '0.02966', '-0.263', '0.1309', '0.1318', '0.1204', '0.1268', '-0.0116', '0.0697', '0.1561', '0.1621', '0.0517', '-0.279', '0.2242', '-0.3247', '-0.0747', '0.004654', '-0.0753', '0.159', '0.04672', '-0.02718', '0.1222', '-0.12115', '-0.07025', '0.1054', '0.09186', '-0.1003', '0.1065', '-0.1421', '-0.09296', '0.228', '0.4314', '0.1478', '0.1282', '-0.00874', '0.05438', '0.03452', '-0.1533', '0.4355', '0.02483', '0.2053', '-0.3782', '0.09216', '-0.02473']",,0009021,C537909,,,,
mondo:0008855,MHC class II deficiency,"['Bare lymphocyte syndrome, type II, complementation group D', 'BARE lymphocyte syndrome, type II, complementation group B, included', 'Bare lymphocyte syndrome 2', 'bare lymphocyte syndrome type II', 'Bare lymphocyte syndrome, type II, complementation group B', 'SCID, HLA CLASS II-NEGATIVE BARE lymphocyte syndrome, type II, complementation group A, included', 'HLA class 2-negative severe combined immunodeficiency', 'BLSII', 'BLS, type II', 'Bare lymphocyte syndrome, type II', 'severe combined immunodeficiency, HLA class ii-negative', 'BARE lymphocyte syndrome, type II', 'Bare lymphocyte syndrome, type II, complementation group C', 'major histocompatibility complex class II expression deficiency', 'BARE lymphocyte syndrome, type II, complementation group C, included', 'SCID, HLA Class 2-negative', 'BARE lymphocyte syndrome', 'BARE lymphocyte syndrome, type II, complementation group D, included', 'BLS', 'BARE lymphocyte syndrome, type II, complementation group E, included', 'BLS type II', 'Bare lymphocyte syndrome', 'Bls, type 2', 'Bare lymphocyte syndrome, type II, complementation group A', 'BLS 2', 'Bare lymphocyte syndrome, type II, complementation group E', 'severe combined immunodeficiency, HLA Class II-negative', 'SCID due to absent class II HLA antigens', 'MHC class II deficiency, complementation group B', 'Bare lymphocyte syndrome type 2', 'HLA class 2-negative SCID', 'immunodeficiency by defective expression of HLA class 2', 'immunodeficiency by defective expression of HLA class type 2', 'MHC class II expression deficiency', 'Bare lymphocyte syndrome, type 2', 'SCID, HLA Class II-negative']",5812,209920,572,CN239286,"['-0.3955', '0.03595', '0.166', '-0.296', '0.08875', '-0.3875', '0.1534', '0.02531', '-0.1548', '0.2001', '-0.1123', '0.1727', '0.1488', '-0.1377', '-0.01116', '-0.1968', '0.1799', '0.1812', '-0.1981', '-0.6836', '-0.158', '-0.4153', '1.014', '-0.1348', '0.2346', '0.05362', '-0.1996', '-0.1047', '-0.4114', '-0.5063', '0.05542', '0.6865', '0.457', '0.3945', '0.1932', '0.01884', '-0.5063', '0.521', '-0.4507', '-0.3606', '-0.1683', '-0.04306', '0.1993', '-0.1095', '-0.43', '-0.517', '-0.0647', '-0.6035', '0.02611', '0.601', '0.12366', '-0.2155', '0.3572', '0.02515', '-0.322', '-0.4795', '-0.1071', '-0.2676', '-0.2328', '0.1847', '-0.0698', '0.2637', '0.3777', '0.495', '0.477', '-0.2032', '0.6333', '0.397', '-0.2153', '0.1381', '0.1139', '-0.283', '0.0681', '0.01985', '0.3267', '0.0715', '0.334', '0.409', '0.0999', '-0.0906', '-0.2896', '-0.2036', '0.171', '0.29', '-0.2761', '-0.391', '0.5127', '0.1642', '0.4993', '-0.1937', '0.294', '0.4536', '0.0474', '-0.08014', '0.4768', '0.8843', '0.2416', '-0.644', '0.00187', '0.2668']",C3895,,D016511,,,,
mondo:0008856,immunodeficiency 27A,"['IMD27A', 'immunodeficiency 27A', 'atypical mycobacterial infection, familial disseminated', 'immunodeficiency 27A, mycobacteriosis, AR', 'IFNGR1 deficiency, autosomal recessive', 'atypical mycobacterial infection, disseminated', 'immunodeficiency 27A, Mycobacteriosis, autosomal recessive', 'atypical mycobacteriosis, familial', 'mycobacterial disease, Mendelian susceptibility to', 'immunodeficiency type 27A']",0111955,209950,99898,C4011949,"['-0.0369', '0.04297', '0.010025', '-0.0171', '0.01628', '-0.02718', '0.01384', '0.0196', '-0.03244', '-0.01933', '-0.02443', '0.0006437', '-0.003506', '0.01098', '-0.007523', '-0.04526', '0.006428', '-0.00887', '-0.0336', '-0.0972', '-0.0136', '-0.007774', '0.06018', '-0.005756', '0.01525', '-0.02335', '-0.005775', '0.012276', '-0.00919', '-0.04318', '0.04535', '0.03403', '0.07513', '0.005516', '0.006786', '0.000753', '-0.02055', '-0.00563', '-0.02106', '-0.07336', '0.01904', '-0.0313', '0.0189', '-0.03207', '-0.0282', '-0.0642', '-0.03818', '0.002827', '0.02408', '0.00335', '-0.01514', '-0.01749', '0.0524', '0.01875', '-0.05075', '-0.02591', '0.02592', '-0.05017', '-0.03528', '-0.001461', '0.0329', '0.0312', '0.01186', '0.015114', '0.0389', '-0.01031', '0.03333', '0.03833', '-0.04227', '0.04764', '-0.063', '0.002628', '0.007717', '-0.01584', '0.02635', '0.011375', '0.02287', '0.009315', '0.02339', '-0.00789', '-0.007557', '0.0003526', '-0.003792', '0.0334', '-0.03604', '0.002222', '0.04907', '0.05493', '0.0473', '0.01073', '0.03552', '0.04837', '0.00211', '0.004375', '0.1196', '0.04785', '0.03247', '-0.076', '-0.004646', '0.02727']",C176806,,,,,,
mondo:0008857,Beemer-Ertbruggen syndrome,"['hydrocephalus, Cardiac malformation, dense bones, etc.', 'hydrocephalus, cardiac malformation, dense bones, etc', 'Beemer lethal malformation syndrome', 'Beemer Ertbruggen syndrome', 'lethal hydrocephalus-cardiac malformation-dense bones syndrome', 'peculiar facial appearance, hydrocephalus, double-outlet right ventricle, genital anomalies and dense bones with lethal outcome']",,209970,1237,C1859526,,,,C537668,,,,
mondo:0008858,Behr syndrome,"['optic atrophy, infantile hereditary, Behr complicated form of', 'optic atrophy, infantile hereditary, with neurologic abnormalities', 'optic atrophy in early childhood, associated with ataxia, spasticity, intellectual disability, and posterior column sensory loss', 'BEHRS', 'Behr syndrome', 'optic atrophy in early childhood, associated with ataxia, spasticity, mental retardation, and posterior column sensory loss']",0111580,210000,1239,C0221061,"['-0.1571', '0.4353', '-0.3003', '-0.04935', '-0.00644', '-0.4958', '-0.2458', '-0.014465', '-0.556', '-0.2048', '-0.191', '-0.1613', '-0.01697', '0.004898', '0.3535', '-0.1191', '-0.2559', '-0.1072', '-0.2186', '-0.526', '-0.2443', '0.006935', '0.02983', '0.03375', '0.1048', '-0.02106', '-0.11176', '0.009224', '0.1332', '0.03296', '0.2428', '0.05453', '0.3767', '-0.1466', '-0.04108', '0.02487', '-0.352', '-0.07733', '-0.1885', '-0.1082', '0.0709', '-0.2603', '-0.008194', '0.092', '0.1703', '-0.4807', '0.01572', '-0.0411', '0.1366', '-0.4634', '0.10754', '0.3772', '-0.2482', '-0.334', '0.343', '-0.109', '0.242', '0.1089', '-0.286', '0.2443', '-0.04233', '0.00389', '0.1277', '0.2449', '-0.3547', '0.3933', '0.1178', '0.2454', '-0.2095', '0.3281', '-0.554', '-0.1179', '0.05505', '-0.1322', '0.4197', '0.2842', '0.3145', '-0.0799', '0.3005', '0.0258', '0.2435', '-0.0697', '-0.2212', '0.5903', '-0.151', '0.1869', '0.0786', '0.3394', '0.3015', '0.4985', '-0.1829', '0.187', '-0.1818', '-0.05948', '0.516', '0.42', '0.2445', '0.05005', '0.224', '0.3342']",C177251,,C537669,,H35.5,,
mondo:0008859,"berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification","['berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification', 'cerebral aneurysm-cirrhosis syndrome']",,210050,,C1859519,,,,C565905,,,,
mondo:0008860,"beta-aminoisobutyric acid, urinary excretion of","['hyper-Beta-aminoisobutyric aciduria', 'BETA-aminoisobutyric aciduria', 'BAIBA', 'beta-aminoisobutyric acid, urinary excretion of', 'Baib urinary excretion', 'Beta-aminoisobutyric aciduria']",,210100,,C1859518,,,,C565904,,,,
mondo:0008861,3-methylcrotonyl-CoA carboxylase 1 deficiency,"['3-MCC deficiency', '3-Methylcrotonyl-Coa carboxylase 1 deficiency', 'Bmcc deficiency', '3-methylcrotonyl-CoA carboxylase 1 deficiency', 'MCCD type 1', 'MCC 1 deficiency', '3-Methylcrotonyl-Coenzyme A carboxylase deficiency', '3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC1', 'deficiency of methylcrotonoyl-Coa carboxylase', '3 alpha methylcrotonylglycinuria 1', 'MCC1D', 'Mccd type 1', '3-METHYLCROTONYL-CoA carboxylase 1 deficiency', 'methylcrotonoyl-CoA carboxylase 1 deficiency', '3-methylcrotonylglycinuria I', '3-Methylcrotonyl-Coa carboxylase deficiency', '3-methylcrotonylglycinuria 1', 'MCC1 deficiency', '3 methylcrotonylglycinuria', 'Methylcrotonyl-Coa carboxylase deficiency', '3 Methylcrotonyl-CoA carboxylase deficiency', '3 Alpha methylcrotonylglycinuria 1', 'methylcrotonylglycinuria type I', 'methylcrotonylglycinuria type 1', 'Mcc1 deficiency', '3 Methylcrotonyl-CoA carboxylase 1 deficiency', '3-methylcrotonylglycinuria', 'MCCC1 3-methylcrotonyl-CoA carboxylase deficiency', 'MCC deficiency']",0080579,210200,,CN028786,,,,C535308,,,,
mondo:0008862,3-methylcrotonyl-CoA carboxylase 2 deficiency,"['MCC2 deficiency', '3-methylcrotonyl-CoA carboxylase deficiency caused by mutation in MCCC2', 'MCCC2 3-methylcrotonyl-CoA carboxylase deficiency', 'methylcrotonylglycinuria, type 2', '3 alpha methylcrotonylglycinuria 2', '3 alpha methylcrotonyl-CoA carboxylase 2 deficiency', 'methylcrotonylglycinuria type 2', 'MCC 2 deficiency', 'MCC2D', '3-Methylcrotonyl-CoA carboxylase 2 deficiency', '3-methylcrotonylglycinuria 2', '3-METHYLCROTONYL-CoA carboxylase 2 deficiency']",0080580,210210,,,,,,C535309,,,,
mondo:0008863,sitosterolemia,"['sitosterolemia', 'phytosterolemia', 'plant sterol storage disease', 'macrothrombocytopenia/stomatocytosis, Mediterranean', 'retention of dietary cholesterol and abnormal retention of non-cholesterol sterols in the body', 'STSL']",0090019,,2882,C0342907,"['-0.4177', '0.2898', '-0.1063', '-0.14', '0.5864', '-0.3743', '-0.593', '-0.2788', '-0.06433', '-0.0772', '-0.1807', '-0.1323', '0.2998', '-0.03', '-0.4077', '0.01549', '-0.03125', '-0.1165', '-0.285', '-0.299', '0.0528', '-0.367', '0.39', '-0.03955', '0.01811', '0.2842', '-0.0457', '0.289', '0.10956', '-0.444', '0.211', '0.0735', '0.473', '0.1838', '0.1065', '-0.3562', '-0.2379', '0.04684', '-0.07513', '-0.792', '-0.3071', '0.02362', '0.3625', '-0.0388', '-0.2496', '-0.4705', '0.3167', '0.03656', '0.467', '-0.1975', '0.1306', '-0.0614', '0.256', '0.3457', '-0.1985', '-0.529', '0.564', '0.194', '-0.704', '0.1029', '0.02185', '0.176', '0.0684', '-0.00465', '0.09375', '-0.2727', '0.2214', '0.2937', '-0.389', '-0.2144', '-0.3938', '-0.2559', '0.04337', '0.4912', '-0.1547', '0.6206', '0.35', '0.3708', '-0.10077', '-0.3604', '0.0632', '-0.3442', '-0.0922', '0.1155', '0.154', '0.5117', '0.3037', '0.4744', '0.0796', '0.0891', '0.1093', '0.1981', '-0.1923', '-0.1216', '0.668', '0.6294', '0.4604', '-0.03357', '-0.2195', '0.282']",C125694,,C537345,,,10063985,
mondo:0008864,Biemond syndrome type 2,"['BIEMOND syndrome II', 'Biemond syndrome type 2', 'hypogonadism-short stature-coloboma-preaxial polydactyly syndrome', 'BS2', 'Biemond syndrome 2', 'iris coloboma, mental retardation, obesity, hypogenitalism, and postaxial polydactyly', 'iris coloboma, intellectual disability, obesity, hypogenitalism, and postaxial polydactyly']",,210350,141333,C1859487,,,,C565902,,,,
mondo:0008865,Bietti crystalline corneoretinal dystrophy,"['Bietti crystalline corneoretinal dystrophy', 'Bietti^s crystalline dystrophy', 'Bietti crystalline retinopathy', 'Bietti crystalline dystrophy', 'Bietti tapetoretinal Degeneration with marginal corneal dystrophy', 'BCD']",0050664,210370,41751,C1859486,"['-0.445', '0.02472', '0.08606', '-0.05365', '0.0998', '-0.3645', '0.011765', '0.1439', '-0.2236', '-0.233', '-0.1168', '-0.0663', '-0.1766', '0.1225', '0.05377', '-0.4744', '0.174', '0.00856', '0.2952', '-0.388', '-0.2167', '-0.2632', '0.0003014', '0.252', '-0.04102', '0.2073', '-0.0682', '0.1533', '-0.2201', '0.2852', '0.2515', '0.01749', '0.0677', '0.2456', '0.0882', '0.185', '0.1906', '-0.01843', '0.0882', '-0.4065', '0.1594', '-0.1112', '0.1361', '0.06226', '-0.1472', '0.05936', '-0.00935', '-0.1256', '0.0679', '0.02522', '0.2416', '0.348', '0.1719', '-0.1958', '-0.0669', '-0.282', '0.5107', '-0.03076', '-0.5938', '-0.007774', '0.04886', '0.02107', '-0.1304', '0.35', '0.0678', '-0.09717', '0.5723', '0.398', '-0.05267', '0.2615', '-0.1976', '-0.165', '0.2532', '-0.1301', '0.1898', '-0.0816', '-0.0858', '0.01196', '-0.2155', '0.02612', '0.2352', '-0.0981', '-0.03558', '0.59', '-0.1091', '-0.4307', '0.06976', '-0.04944', '0.249', '-0.11444', '0.1827', '0.4136', '0.1193', '0.2129', '0.4424', '-0.02571', '0.3572', '-0.1418', '-0.0405', '0.2157']",C179299,,C535440,,,,
mondo:0008866,"bifid nose, autosomal recessive","['Nose, Median cleft of', 'median fissure of Nose', 'autosomal recessive bifid nose', 'bifid nose, autosomal recessive']",,210400,,,,,,,,,,
mondo:0008867,biliary atresia,"['congenital biliary atresia', 'atresia of bile ducts', 'atresia of bile duct', 'isolated atresia of bile ducts', 'non-syndromic biliary atresia', 'biliary atresia, congenital', 'isolated biliary atresia']",13608,,30391,C0005411,,C34421,,D001656,751.61,,10003650,
mondo:0008868,biliary malformation with renal tubular insufficiency,"['cholestatic jaundice and renal tubular insufficiency', 'biliary malformation with renal tubular insufficiency']",,210550,,C0400972,,,,C537726,,,,
mondo:0008869,Seckel syndrome 1,"['microcephalic primordial dwarfism I', 'nanocephalic dwarfism', 'Seckel syndrome caused by mutation in ATR', 'Seckel-type dwarfism', 'Seckel syndrome type 1', 'Seckel syndrome 3', 'Bird-headed dwarfism', 'Seckel syndrome 1', 'ATR Seckel syndrome', 'SCKL1', 'Sckl', 'microcephalic primordial dwarfism 1']",0070007,210600,,CN033164,,,,,,,,
mondo:0008870,"bird headed-dwarfism, Montreal type","['premature senility, premature graying and loss of scalp hair and wrinkled skin of the palms', 'Bird-headed dwarfism, Montreal type', 'premature senility, premature greying and loss of scalp hair and wrinkled skin of the palms', 'microcephalic primordial dwarfism, Montreal type', 'Bird-headed dwarfism with features of premature senility']",,210700,2617,C1859468,,,,C535448,,,,
mondo:0008871,microcephalic osteodysplastic primordial dwarfism type I,"['osteodysplastic primordial dwarfism type I', 'Brachymelic primordial dwarfism', 'MOPD 1', 'Cephaloskeletal dysplasia', 'microcephalic osteodysplastic primordial dwarfism, type 1', 'microcephalic osteodysplastic primordial dwarfism, type I', 'MOPD1', 'osteodysplastic primordial dwarfism, type 1', 'Taybi-Linder syndrome', 'brachymelic primordial dwarfism', 'low-birth-weight dwarfism with skeletal dysplasia', 'cephaloskeletal dysplasia']",0060608,210710,,,,,,,,,,
mondo:0008872,microcephalic osteodysplastic primordial dwarfism type II,"['Mopd 2', 'microcephalic osteodysplastic primordial dwarfism with tooth abnormalities', 'MOPD II', 'microcephalic osteodysplastic primordial dwarfism type 2', 'osteodysplastic primordial dwarfism type II', 'osteodysplastic primordial dwarfism, type 2', 'microcephalic osteodysplastic primordial dwarfism, type II', 'Majewski osteodysplastic primordial dwarfism type II', 'microcephalic osteodysplastic primordial dwarfism, type 2', 'MOPD2', 'osteodysplastic primordial dwarfism type 2', 'MOPD type II']",0060609,210720,2637,,"['0.1705', '0.5425', '-0.2612', '-0.00568', '0.7773', '0.00724', '-0.0709', '1.073', '-0.7554', '-0.7827', '-0.0626', '-0.2167', '0.2515', '0.2666', '-0.2415', '-0.622', '0.6543', '0.05228', '-0.2559', '-0.7397', '-0.873', '0.087', '0.9355', '0.0796', '-0.1074', '-0.2854', '-0.12286', '-0.2428', '0.5977', '-0.11237', '0.3867', '-0.22', '-0.1353', '-0.002241', '-0.436', '0.0747', '-0.1184', '0.2651', '0.1527', '-0.4202', '0.04672', '0.1969', '-0.5405', '-0.1477', '0.3313', '-0.02153', '-0.0429', '0.0915', '0.1823', '-0.2522', '-0.04257', '0.02206', '-0.755', '-0.002672', '-0.0687', '-0.484', '-0.3887', '-0.455', '0.637', '0.1099', '-0.2416', '0.3608', '-0.3428', '0.313', '-0.1425', '0.9976', '-0.04904', '0.1743', '-0.2822', '0.4045', '0.05133', '-0.1061', '0.1744', '-0.852', '0.04013', '-0.0203', '-0.2554', '0.2576', '-0.3352', '0.04147', '-0.7183', '0.1725', '-0.0428', '0.0727', '-0.1876', '-0.10443', '0.4375', '0.1006', '1.049', '0.439', '0.1132', '-0.09424', '-0.5327', '-0.681', '0.4395', '-0.4634', '0.263', '0.2559', '0.874', '-0.0468']",,,C565898,,,,
mondo:0008873,"microcephalic osteodysplastic primordial dwarfism, type 3","['microcephalic osteodysplastic primordial dwarfism, type III', 'microcephalic osteodysplastic primordial dwarfism, Caroline Crachami type', 'Mopd, Caroline Crachami type', 'Mopd, Sicilian fairy type', 'microcephalic osteodysplastic primordial dwarfism, Sicilian fairy type', 'osteodysplastic primordial dwarfism, type 3', 'Mopd 3']",,210730,,C1859439,,,,C537320,,,,
mondo:0008874,Bangstad syndrome,"['Bangstad syndrome', 'Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goitre and primary gonadal insufficiency', 'Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter and primary gonadal insufficiency', 'Bird-headed dwarfism with progressive ataxia, insulin-resistant diabetes, goiter, and primary gonadal insufficiency', 'ataxia-diabetes-goiter-gonadal insufficiency syndrome']",,210740,1227,C0342284,,,,C537902,759.89,,,
mondo:0008875,blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome,"['blepharophimosis with ptosis, syndactyly, and short stature', 'Frydman-Cohen-Karmon syndrome', 'blepharophimosis - ptosis - esotropia - syndactyly - short stature', 'Frydman Cohen Karmon syndrome']",,210745,2057,,,,,C536235,,,,
mondo:0008876,Bloom syndrome,"['MGRISCE1', 'BLS', 'congenital telangiectatic erythema', 'growth deficiency, sun-sensitive, telangiectatic, hypo and hyperpigmented skin, predisposition to malignancy and chromosomal instability', 'BS', 'Bloom-Torre-Machacek syndrome', 'BLM', 'microcephaly, growth restriction, and increased sister chromatid exchange 1', 'BSyn', 'congenital telangiectatic erythema syndrome', 'Bloom syndrome']",2717,210900,125,C0005859,"['0.1471', '0.2252', '-0.3867', '0.0544', '0.5015', '-0.4006', '0.6553', '0.8525', '-0.547', '-0.6055', '0.3416', '0.8184', '0.53', '-0.2783', '-0.3894', '0.1995', '0.617', '0.5615', '-1.066', '-0.2996', '-0.1648', '-0.4944', '0.4314', '0.081', '0.1521', '0.0701', '-0.6123', '-0.313', '-0.689', '-0.5596', '0.9365', '-0.387', '0.783', '0.00915', '0.2269', '0.522', '-0.3198', '-0.382', '-0.717', '0.3643', '-0.371', '-0.1761', '-0.02318', '-0.7163', '0.1254', '-0.0733', '0.04126', '0.3708', '0.665', '-0.2878', '-0.4841', '-0.3977', '0.00497', '0.0426', '-0.4402', '0.6177', '0.4307', '-0.3152', '-0.2274', '0.2231', '0.267', '0.4758', '-0.9243', '-0.2913', '0.2954', '0.4373', '-0.176', '0.191', '0.522', '0.5796', '0.08344', '-0.1407', '-0.2126', '-0.03787', '0.179', '-0.1592', '-0.02916', '-0.217', '-0.2493', '-0.2627', '0.05948', '-0.01865', '-0.332', '0.2642', '-0.2834', '-0.2559', '0.0675', '0.2328', '0.6387', '-0.1232', '0.329', '-0.008', '-0.3015', '0.1019', '0.05807', '-0.02277', '0.1342', '-0.2438', '-0.1136', '0.1003']",C2903,,D001816,757.39,Q82.2,,
mondo:0008877,blue diaper syndrome,"['familial hypercalcemia-nephrocalcinosis-indicanuria syndrome', 'hypercalcemia, familial, with nephrocalcinosis and indicanuria', 'blue diaper syndrome', 'Drummond syndrome']",,211000,94086,C0268478,,,,C536239,,,,
mondo:0008878,"bone dysplasia, lethal Holmgren type","['autosomal recessive lethal chondrodysplasia, round femoral inferior epiphysis type', 'bone dysplasia, lethal, Holmgren type', 'bone dysplasia lethal Holmgren type']",,211120,1842,C1859407,,,,C565896,,,,
mondo:0008879,Bowen-Conradi syndrome,"['Bowen syndrome, Hutterite type', 'Bowen Hutterite syndrome (formerly)', 'Bowen Hutterite syndrome, formerly', 'Bowen-Conradi syndrome', 'Bowen-Conradi Hutterite syndrome', 'Bowen Hutterite syndrome', 'BWCNS']",0050684,211180,1270,C1859405,"['-0.453', '-0.1177', '-0.3848', '-0.01859', '0.3057', '-1.122', '0.2467', '1.0625', '-0.4312', '-0.888', '0.0649', '-0.1958', '-0.1087', '-0.05588', '-0.07874', '0.4792', '0.3528', '-0.7056', '-0.3499', '-0.2417', '-0.0368', '0.2325', '0.621', '-0.1558', '-0.0315', '-0.2168', '0.1484', '0.2205', '0.3398', '-0.0464', '0.1791', '0.04083', '0.0503', '0.6167', '-0.1573', '0.2239', '0.1494', '-0.2524', '-0.1262', '-0.01049', '-0.4937', '-0.4062', '-0.3796', '-0.282', '0.1515', '-0.03564', '-0.3167', '0.0979', '-0.3718', '0.1804', '-0.5674', '-0.533', '-0.0788', '-0.1163', '-0.3164', '0.04996', '0.02226', '-0.0942', '-0.03455', '0.11774', '0.1263', '-0.07825', '-0.256', '0.2544', '0.219', '0.236', '-0.1884', '0.03125', '-0.7173', '0.1727', '-0.487', '0.4172', '-0.09625', '0.1653', '-0.425', '0.4248', '0.1057', '-0.4788', '-0.816', '0.1743', '-0.1064', '-0.04544', '-0.4995', '0.6855', '-0.08936', '-0.002375', '0.4485', '0.3755', '0.3245', '0.1891', '0.529', '0.0664', '0.12445', '0.2152', '0.1043', '-0.05734', '0.3943', '-0.67', '0.4453', '0.295']",,,C537081,759.89,,,
mondo:0008880,Bowen syndrome of multiple malformations,"['Bowen syndrome of multiple malformations', 'Bowen syndrome']",,211200,1271,C1859404,,,,C538164,,,,
mondo:0008881,kyphomelic dysplasia,"['kyphomelic dysplasia', 'congenital bowing with short bones', 'bowing, congenital, with short bones']",,211350,1801,C0432239,,,,C538128,733.29,,,
mondo:0008882,congenital bowing of long bones,"['bowing of long bones, asymmetric and symmetric', 'bowing of long bones congenital']",,211355,2292,,,,,,,,10054064,
mondo:0008883,"brachydactyly, type A2, with microcephaly","['brachydactyly, type A2, with microcephaly']",,211369,,C1859393,,,,C565894,,,,
mondo:0008884,oculoosteocutaneous syndrome,"['oculoosteocutaneous syndrome', 'BRACHYMETAPODY-anodontia-hypotrichosis-ALBINOIDISM', 'anodontia-hypotrichosis syndrome', 'brachymetapody anodontia hypotrichosis albinoidism']",,211370,2713,C1859385,,,,C565893,,,,
mondo:0008885,Elsahy-Waters syndrome,"['hypospadias, hypertelorism, upper lid coloboma, and mixed-type hearing loss', 'hypospadias-hypertelorism-coloboma and deafness syndrome', 'ELSAHY-Waters syndrome', 'branchio-skeleto-genital syndrome', 'ESWS', 'Elsahy-Waters syndrome', 'brachioskeletogenital syndrome', 'BSG syndrome', 'hypospadias, hypertelorism, upper 51D coloboma, and mixed-type hearing loss']",0080631,603463,157788,C1863870,"['-0.2499', '-0.05157', '0.4941', '-0.4248', '0.3281', '-0.3452', '-0.0762', '0.4805', '-0.5317', '-0.2979', '-0.2505', '-0.271', '0.027', '-0.325', '-0.3645', '-0.05106', '0.2118', '-0.1458', '-0.5645', '-0.319', '-0.02007', '0.06073', '0.4358', '-0.3833', '0.3853', '-0.1387', '-0.345', '-0.1267', '0.622', '-0.432', '0.05893', '-0.34', '-0.06076', '0.1111', '0.3752', '-0.2773', '-0.2394', '-0.2301', '-0.1901', '-0.441', '0.3735', '0.206', '0.01164', '-0.6963', '0.1454', '-0.4263', '0.0358', '0.2583', '-0.4165', '-0.012726', '-0.2128', '-0.04562', '0.132', '0.1979', '-0.4165', '-0.525', '-0.002035', '-0.3494', '-0.2803', '0.11597', '0.2878', '-0.0217', '-0.3152', '0.07544', '-0.0759', '-0.1318', '0.2915', '0.4065', '-0.2559', '0.2292', '-0.3953', '0.2646', '0.07465', '-0.334', '-0.1572', '-0.2498', '0.2286', '-0.1372', '-0.3518', '0.10394', '0.11475', '0.161', '-0.095', '0.877', '-0.075', '-0.05887', '-0.10364', '0.1906', '-0.005444', '0.1738', '-0.5293', '0.719', '0.3796', '0.4077', '0.7793', '-0.3533', '0.4846', '-0.6357', '0.555', '0.07416']",,,C566373,,,,
mondo:0008886,Sabinas brittle hair syndrome,"['Sabinas brittle hair syndrome', 'Sabinas syndrome', 'brittle hair and mental Deficit', 'brittle hair syndrome, Sabinas type']",0111874,211390,3123,C0796271,,,,C536320,,,,
mondo:0008887,bronchiectasis with or without elevated sweat chloride 1,"['BESC1', 'bronchiectasis with or without elevated sweat chloride type 1', 'bronchiectasis with or without elevated sweat chloride 1, modifier of', 'bronchiectasis with or without elevated sweat chloride 1', 'cystic fibrosis-like syndrome']",0080526,211400,,C2749757,,,,C567618,,,,
mondo:0008888,Williams-Campbell syndrome,"['Williams-Campbell syndrome', 'tracheobronchomalacia', 'BRONCHOMALACIA']",,211450,411501,,,,,,748.3,,,
mondo:0008889,thromboangiitis obliterans,"['inflammatory occlusive peripheral vascular disease', 'TAO', 'occlusive peripheral vascular disease', 'Buerger^s disease', 'thromboangiitis obliterans', 'thromboangiitis obliterans [Buerger^s disease]', 'presenile gangrene', 'BUERGER disease']",12918,211480,36258,C0040021,,C35070,1001211,D013919,443.1,,10043540,
mondo:0008890,progressive bulbar palsy,"['progressive bulbar atrophy', 'Fazio-Londe disease', 'bulbar palsy, progressive, of childhood']",681,,,C0030442,"['-0.2101', '0.2334', '0.0929', '-0.413', '-0.2908', '-0.2009', '0.3071', '0.013626', '-0.874', '-0.0381', '-0.01363', '-0.3252', '-0.1011', '0.1594', '0.32', '-0.2205', '-0.1864', '-0.598', '-0.1659', '-0.1696', '0.1757', '-0.37', '-0.09247', '0.285', '-0.1531', '-0.2184', '0.3196', '-0.08545', '-0.317', '0.6875', '-0.3213', '0.002588', '0.1376', '-0.212', '0.5684', '-0.2128', '0.05463', '0.2874', '0.06696', '-0.766', '-0.1368', '-0.3972', '-0.0757', '0.01929', '0.2236', '0.02676', '-0.3184', '-0.03366', '-0.0891', '0.457', '-0.0181', '0.1709', '-0.02632', '-0.10956', '-0.0759', '-0.3413', '-0.13', '-0.11163', '-0.2751', '0.2644', '-0.11084', '0.1595', '0.3232', '0.3264', '-0.4453', '0.2241', '0.2537', '0.1808', '-0.2646', '0.737', '-0.2157', '0.0901', '0.12494', '-0.2986', '0.3896', '0.2974', '0.06183', '0.271', '-0.0447', '-0.1663', '-0.01203', '-0.5347', '0.22', '0.477', '-0.4434', '0.2115', '-0.2524', '0.3455', '0.6523', '-0.1432', '-0.1244', '-0.1625', '0.1396', '0.077', '0.3984', '0.00551', '-0.05548', '-0.01965', '-0.04156', '0.5264']",C85026,0003783,D010244,335.22,G12.22,,
mondo:0008891,riboflavin transporter deficiency,"['BVVLS', 'disorder of riboflavin transmembrane transporter activity', 'Fazio-Londe syndrome', 'Brown-Vialetto-Van Laere syndrome 1', 'pontobulbar palsy and neurosensory deafness', 'progressive bulbar palsy with sensorineural deafness', 'BVVLS1', 'riboflavin transmembrane transporter activity disease', 'Brown-Vialetto-van Laere syndrome', 'sensorineural hearing loss-pontobulbar palsy syndrome']",0050694,,97229,,"['-0.614', '-0.3123', '-0.2479', '0.314', '0.12036', '-0.1093', '0.1252', '1.107', '-0.973', '-0.3542', '-0.11646', '-0.55', '-0.7153', '0.4868', '0.3037', '-0.1855', '-0.5405', '-0.6943', '-0.364', '-0.562', '0.486', '-0.9697', '0.3704', '0.2942', '-0.5405', '0.1388', '-0.2284', '-0.05487', '-0.1833', '0.2502', '0.2642', '0.302', '0.1464', '-0.3347', '-0.6724', '-0.3696', '-0.03082', '-0.6567', '-0.05707', '-0.0008235', '-0.2527', '-0.1515', '0.5605', '0.4858', '-0.1644', '-0.1963', '-0.53', '-0.489', '-0.1936', '0.7417', '-0.4875', '-0.4446', '-0.0659', '-0.4507', '0.427', '-0.8105', '0.2803', '-0.214', '0.1742', '0.553', '0.3105', '0.5254', '0.04056', '0.3252', '-0.477', '0.3804', '-0.0828', '0.4768', '0.1139', '0.0824', '0.1411', '-0.1805', '-0.4653', '-0.3716', '0.378', '-0.11365', '0.638', '0.2537', '0.003815', '0.2197', '0.296', '0.04636', '-0.307', '1.31', '-0.4517', '0.2441', '0.3083', '0.2422', '0.956', '0.1533', '0.3772', '0.3025', '0.1735', '-0.2837', '0.548', '-0.3093', '0.3', '-0.11523', '-0.267', '0.3357']",,,C537111,,,,
mondo:0008892,progressive familial intrahepatic cholestasis type 1,"['cholestasis, progressive familial intrahepatic 1', 'cholestasis, progressive familial intrahepatic, type 1', 'severe ATP8B1 deficiency', 'PFIC1', 'FIC1 deficiency', 'Byler disease', 'cholestasis, fatal intrahepatic', 'Byler^s disease', 'cholestasis, progressive familial intrahepatic, 1', 'progressive familial intrahepatic cholestasis']",0070226,211600,79306,CN205891,"['0.2421', '0.158', '0.0777', '-0.01875', '-0.1146', '-0.3638', '-0.222', '0.4111', '0.2349', '0.1655', '-0.3225', '-0.03885', '-0.3958', '0.263', '-0.59', '-0.256', '0.2031', '-0.4775', '0.09283', '-1.026', '-0.2966', '-0.29', '0.4504', '-0.1779', '-0.1533', '-0.1669', '0.1548', '0.593', '-0.1729', '-0.163', '0.4958', '0.142', '0.1372', '0.4421', '-0.3567', '-0.601', '-0.175', '0.1212', '-0.01021', '0.5674', '-0.06885', '-0.0614', '0.585', '0.3433', '-0.0659', '0.1647', '0.1606', '-0.2075', '0.010025', '-0.3389', '0.010994', '0.0783', '0.457', '-0.745', '0.1515', '-0.1095', '0.07733', '-0.1964', '-0.4973', '0.361', '0.866', '-0.05597', '0.7285', '0.0852', '0.576', '-0.1287', '0.8525', '0.3237', '-0.1045', '0.688', '0.1548', '-0.07007', '0.1547', '-0.6694', '0.596', '0.2542', '0.0872', '0.01478', '-0.10846', '0.0777', '0.38', '-0.1142', '-0.9287', '-0.12195', '-0.687', '0.116', '0.3281', '-0.3152', '0.213', '-0.0985', '0.852', '0.1743', '-0.3232', '0.5586', '0.498', '0.2057', '0.3289', '-0.864', '-0.02489', '-0.3188']",,,,,,,
mondo:0008893,C syndrome,"['C syndrome', 'Opitz trigonocephaly C syndrome', 'trigonocephaly C syndrome', 'trigonocephaly syndrome', 'OTCS', 'Opitz trigonocephaly syndrome', 'Opitz C trigonocephaly']",0111581,211750,1308,C0796095,"['0.02202', '0.1493', '-0.0506', '-0.63', '-0.08563', '-0.1603', '0.2462', '0.4895', '-0.583', '-0.6724', '0.0995', '-0.5264', '-0.3062', '-0.3572', '-0.5757', '0.01513', '0.010574', '-0.477', '-0.3848', '-0.4888', '0.02142', '0.5166', '0.47', '0.1786', '0.24', '-0.1902', '-0.2168', '0.201', '1.221', '0.06604', '0.407', '-0.503', '0.65', '0.176', '0.04343', '-0.5986', '-0.4053', '-0.1154', '-0.3335', '0.07227', '0.2517', '-0.2522', '-0.04373', '-0.1073', '0.3684', '-0.0765', '0.1897', '0.847', '-0.534', '-0.1307', '-0.3062', '0.1986', '-0.1239', '0.2693', '-1.22', '-0.033', '-0.1318', '-0.04633', '-0.2625', '0.3232', '-0.1439', '-0.1182', '-0.0978', '0.3894', '0.3745', '-0.4775', '0.5894', '0.6846', '-0.995', '0.3137', '-0.371', '0.2026', '-0.0886', '0.1622', '-0.3044', '0.659', '0.1334', '-0.216', '-0.4773', '-0.1613', '0.05862', '0.708', '0.08514', '0.2336', '0.2869', '0.11993', '0.2423', '0.3445', '-0.2344', '0.2886', '-0.3716', '0.2178', '0.1364', '0.5615', '0.5977', '0.1893', '0.525', '-0.2961', '0.4407', '-0.05756']",,,C537418,,,,
mondo:0008894,cataract-hypertrichosis-intellectual disability syndrome,"['cataract, hypertrichosis, mental retardation syndrome', 'cataract, hypertrichosis, intellectual disability syndrome', 'CAHMR syndrome']",,211770,1375,C0796282,,,,C537959,,,,
mondo:0008895,hereditary arterial and articular multiple calcification syndrome,"['CALJA', 'arterial calcification due to deficiency of Cd73', 'arterial calcification and distal joint calcification', 'calcification of joints and arteries', 'arterial calcification due to CD73 deficiency', 'ACDC']",0111582,211800,289601,C4305347,"['-0.1886', '-0.1132', '-0.08527', '-0.208', '0.2395', '-0.791', '-0.2115', '0.506', '-0.5356', '-0.3035', '-0.3462', '-0.02324', '-0.05807', '0.2147', '0.10614', '0.0937', '0.2345', '0.1302', '0.5347', '-0.4963', '-0.137', '-0.101', '0.3186', '-0.2842', '-0.1037', '0.75', '0.2747', '0.506', '0.1024', '0.07416', '0.3413', '-0.1082', '0.183', '0.2418', '0.1772', '-0.2412', '-0.2391', '-0.12115', '0.4236', '-0.12036', '-0.1327', '-0.687', '0.2354', '0.1616', '0.501', '-0.28', '-0.4124', '0.5415', '-0.007755', '-0.2712', '0.161', '0.461', '0.08057', '-0.12476', '-0.2805', '-0.7085', '0.303', '-0.1587', '0.1794', '-0.572', '0.4192', '0.253', '-0.3188', '-0.261', '-0.1816', '0.1577', '0.1317', '0.6924', '-0.1335', '0.1846', '-0.1527', '-0.1694', '0.0843', '-0.0695', '0.0914', '0.541', '-0.2155', '0.561', '-0.3237', '-0.2174', '-0.4832', '0.04782', '0.438', '0.202', '0.2498', '0.2825', '-0.0583', '0.2485', '-0.1945', '-0.2455', '0.4487', '0.3584', '0.0758', '0.2352', '0.9253', '0.089', '0.883', '-0.2795', '-0.2465', '-0.2598']",,,C565891,,,,
mondo:0008896,"campomelia, Cumming type","['campomelia, Cumming type', 'campomelia, cervical lymphocele, polysplenia, and multicystic dysplastic kidneys', 'Cumming syndrome', 'campomelia Cumming type', 'cervical lymphocele with bowed long bones']",,211890,1318,C1859371,,,,C537966,,,,
mondo:0008898,"camptodactyly syndrome, Guadalajara type 1","['faciothoracoskeletal syndrome', 'GCS1', 'GCS 1', 'FTSS', 'camptodactyly syndrome, Guadalajara, type I', 'camptodactyly syndrome Guadalajara type 1', 'camptodactyly syndrome, Guadalajara, type 1']",,211910,1327,C1859359,,,,C537970,,,,
mondo:0008899,"camptodactyly syndrome, Guadalajara type 2","['camptodactyly syndrome, Guadalajara, type II', 'camptodactyly syndrome Guadalajara type 2', 'Guadalajara camptodactyly syndrome type II', 'camptodactyly syndrome, Guadalajara, type 2']",,211920,1326,,,,,C567138,,,,
mondo:0008900,camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia,"['camptodactyly with fibrous tissue hyperplasia and skeletal dysplasia', 'camptodactyly, fibrous tissue hyperplasia, and skeletal dysplasia']",,211930,1321,,,,,C537974,,,,
mondo:0008901,Tel Hashomer camptodactyly syndrome,"['Tel Hashomer camptodactyly syndrome', 'camptodactyly with muscular hypoplasia, skeletal dysplasia, and abnormal palmar creases']",,211960,3292,C1859356,,,,C536953,,,,
mondo:0008902,camptodactyly-ichthyosis syndrome,"['camptodactyly ichthyosis syndrome', 'camptodactyly-ichthyosis syndrome']",,211965,,C1859355,,,,C537976,,,,
mondo:0008903,lung cancer,"['lung cancer, protection against', 'malignant lung tumour', 'alveolar cell carcinoma', 'lung neoplasm', 'nonsmall cell lung cancer, susceptibility to, autosomal dominant, somatic mutation', 'Nonsmall cell lung cancer', 'lung cancer, resistance to, autosomal dominant, somatic mutation', 'malignant tumour of the lung', 'lung cancer, somatic', 'nonsmall cell lung cancer, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation', 'malignant lung neoplasm', 'cancer of lung', 'lung cancer, susceptibility to, autosomal dominant, somatic mutation', 'adenocarcinoma of lung, somatic', 'malignant lung tumor', 'malignant tumor of the lung', 'malignant neoplasm of the lung', 'adenocarcinoma of lung, response to tyrosine kinase inhibitor in, autosomal dominant, somatic mutation', 'lung cancer, protection against, autosomal dominant, somatic mutation', 'malignant tumor of lung', 'malignant neoplasm of lung', 'lung cancer', 'malignant tumour of lung', 'nonsmall cell lung cancer, somatic']",1324,211980,,,"['0.011154', '0.03973', '-0.02153', '-0.001952', '0.003057', '-0.05786', '0.02255', '0.02971', '-0.03662', '-0.04236', '0.002787', '0.005524', '-0.000327', '0.001718', '-0.0321', '-0.0433', '-0.00697', '-0.00685', '-0.01233', '-0.071', '-0.02129', '-0.01587', '0.02916', '-0.0241', '0.03888', '-0.03592', '-0.01443', '0.006477', '0.005264', '-0.0429', '0.04385', '0.000996', '0.04938', '-0.008', '0.01694', '-0.0236', '-0.02733', '-0.02179', '0.00691', '-0.006905', '0.02155', '-0.04245', '0.00946', '-0.03687', '-0.004753', '-0.007565', '-0.01877', '0.03482', '0.019', '0.01901', '-0.01089', '-0.005108', '0.01936', '0.01588', '-0.02892', '-0.00849', '0.01897', '-0.02083', '-0.079', '-0.02097', '0.0261', '0.01672', '0.01112', '0.002335', '-0.01232', '0.004017', '0.05167', '0.03033', '-0.03885', '0.03064', '-0.01851', '0.0016775', '0.01492', '-0.01874', '0.03552', '0.003845', '-0.005314', '-0.0143', '-0.01683', '-0.0349', '-0.03004', '0.003477', '-0.01666', '0.02296', '-0.03143', '-0.02039', '0.02246', '0.02826', '0.0619', '-6e-08', '0.01689', '0.0333', '-0.01808', '-0.00374', '0.0805', '0.0454', '0.02507', '-0.03162', '-0.01826', '0.00958']",C7377,,,162.9,,,
mondo:0008904,"camptomelic syndrome, long-limb type","['campomelic syndrome, long-limb type', 'campomelic syndrome long limb type', 'Camptomelic syndrome long limb type', 'camptomelic syndrome, long-limb type']",,211990,,C1859354,,,,C537977,,,,
mondo:0008905,predisposition to invasive fungal disease due to CARD9 deficiency,"['CARD9 immunodeficiency', 'invasive candidiasis-deep dermatophytosis syndrome', 'candidiasis, familial, 2, autosomal recessive', 'candidiasis, familial, 2', 'CANDF2', 'CARD9 deficiency', 'candidiasis familial chronic mucocutaneous, autosomal recessive', 'candidiasis, familial chronic mucocutaneous, autosomal recessive', 'candidiasis, familial, type 2']",,212050,457088,C1859353,,,,,,,,
mondo:0008907,PMM2-congenital disorder of glycosylation,"['PMM2-CDG', 'PMM2-CDG (CDG-Ia)', 'Jaeken syndrome', 'CDG-IA', 'carbohydrate deficient glycoprotein syndrome type Ia', 'phosphomannomutase 2 deficiency', 'congenital disorder of glycosylation type Ia', 'carbohydrate-deficient glycoprotein syndrome type 1A', 'congenital disorder of glycosylation type 1a', 'carbohydrate-deficient glycoprotein syndrome, type Ia, formerly', 'congenital disorder of glycosylation, type Ia', 'carbohydrate-deficient glycoprotein syndrome, type Ia', 'carbohydrate-deficient glycoprotein syndrome type 1A (formerly)', 'CDG 1A', 'CDG syndrome type Ia', 'CDG1A']",0080552,212065,79318,C0349653,"['-0.5083', '0.25', '0.12177', '-0.1079', '0.2632', '-0.8296', '-0.1528', '0.325', '-0.1609', '0.2183', '0.07007', '-0.2037', '-0.131', '0.00413', '-0.3044', '-0.0988', '0.3726', '-0.1381', '-0.2598', '-0.11816', '-0.00529', '-0.594', '0.2969', '-0.1669', '0.159', '-0.4395', '-0.09076', '-0.2522', '0.3582', '-0.443', '0.8496', '-0.04346', '0.521', '0.1192', '0.04965', '0.1128', '-0.3005', '0.05225', '-0.4124', '-0.03302', '0.0115', '-0.511', '-0.3386', '0.4368', '-0.2007', '0.0772', '0.2576', '0.0794', '-0.1627', '0.03543', '-0.093', '-0.00726', '0.1755', '0.03204', '-0.1884', '-0.3352', '0.03702', '-0.2866', '-0.347', '0.255', '0.1516', '-0.255', '-0.2876', '0.1067', '0.01199', '-0.503', '0.404', '-0.0732', '0.1044', '0.02159', '0.03363', '0.284', '0.1965', '-0.0501', '-0.05548', '-0.2274', '0.12384', '-0.26', '-0.2524', '0.0551', '-0.1366', '-0.54', '-0.0735', '-0.0349', '-0.2264', '-0.1508', '-0.1459', '0.005898', '0.3157', '0.4482', '0.3462', '0.4712', '0.4253', '-0.0402', '0.525', '0.0596', '0.2491', '-0.3135', '0.5986', '0.2634']",C126868,,C535739,,,,
mondo:0008908,MGAT2-congenital disorder of glycosylation,"['CDG IIa', 'intellectual disability, Growth retardation, prominent columella, and open mouth', 'congenital disorder of glycosylation type 2a', 'CDG syndrome type IIa', 'carbohydrate deficient glycoprotein syndrome type IIa', 'CDGS2', 'carbohydrate-deficient glycoprotein syndrome, type II, formerly', 'CDG 2A', 'N-acetylglucosaminyltransferase 2 deficiency', 'congenital disorder of glycosylation type IIa', 'congenital disorder of glycosylation, type IIa', 'carbohydrate-deficient glycoprotein syndrome, type II, formerly; CDGS2, formerly', 'Alkuraya syndrome', 'mental retardation, Growth retardation, prominent columella, and open mouth', 'carbohydrate-deficient glycoprotein syndrome, type II', 'MGAT2-CDG', 'CDG2A', 'MGAT2-CDG (CDG-IIa)', 'CDG-IIa', 'carbohydrate-deficient glycoprotein syndrome type 2']",0070253,212066,79329,C2931008,"['-0.6646', '0.1833', '0.495', '-0.1425', '0.2097', '0.08405', '-0.2377', '0.002245', '-0.597', '0.1178', '-0.191', '-0.2032', '0.3044', '-0.539', '-0.02542', '0.218', '0.2462', '-0.1417', '0.03195', '-0.7876', '0.2117', '0.0009503', '0.1774', '-0.2515', '0.575', '-0.3184', '-0.42', '-0.08923', '0.5024', '-0.181', '-0.1923', '0.08435', '0.3494', '0.3867', '-0.0899', '-0.3945', '0.0685', '0.1404', '-0.2595', '-0.549', '0.02127', '-0.3506', '-0.2773', '-0.0787', '-0.2134', '-0.1199', '0.2307', '0.1722', '0.2644', '0.2346', '-0.3933', '-0.02776', '-0.06073', '0.554', '-0.317', '-0.4568', '0.213', '0.10425', '-0.12256', '0.4233', '-0.1063', '-0.1296', '-0.1017', '-0.425', '-0.0809', '-0.1519', '0.09564', '-0.0175', '-0.6577', '0.3125', '-0.3777', '0.304', '0.3506', '0.224', '0.11285', '0.1582', '0.7124', '0.06964', '-0.3035', '0.2301', '-0.1372', '-0.4504', '0.1121', '0.4404', '-0.1472', '0.11633', '-0.2434', '0.441', '0.4922', '0.04666', '-0.4065', '0.903', '0.4097', '-0.04773', '0.5044', '0.6104', '0.1956', '-0.4185', '0.3499', '0.1802']",,,C535752,,,,
mondo:0008909,"congenital disorder of glycosylation, type i/IIx","['congenital disorder of glycosylation, type i/IIx', 'congenital disorder of glycosylation type I/IIX', 'CDG-X', 'CDG X']",,212067,,C0349655,,,,C562844,,,,
mondo:0008910,carboxypeptidase N deficiency,['carboxypeptidase N deficiency'],0111583,212070,,C0398782,,C132196,,C562876,279.8,,,
mondo:0008911,"cardiac lipidosis, familial","['cardiac lipidosis, familial']",,212080,,C1859332,,,,C565884,,,,
mondo:0008912,cardiac septal defects with coarctation of the aorta,['cardiac septal defects with coarctation of the aorta'],,212090,,C1859331,,,,C565883,,,,
mondo:0008913,"cardiac valvular defect, developmental","['CARDIAC valvular defect, developmental', 'CVDD', 'cardiac valvular defect, developmental']",0080633,212093,,C1859330,"['-0.02757', '0.04312', '0.01959', '-0.02498', '0.02109', '-0.06012', '0.009186', '0.07855', '-0.04742', '-0.02753', '-0.02315', '-0.0353', '0.01231', '0.0174', '-0.02864', '-0.0315', '-0.02388', '-0.01657', '-0.03384', '-0.1023', '0.0166', '0.001483', '0.05273', '-0.02037', '0.01736', '-0.03044', '-0.001957', '0.0089', '0.0253', '-0.03345', '0.05432', '0.004044', '0.08496', '0.02827', '0.00946', '-0.01234', '0.003654', '-0.02194', '-0.01588', '-0.05643', '0.04562', '-0.03955', '0.022', '0.0051', '-0.01534', '-0.03815', '-0.003077', '0.05045', '-0.009346', '0.02881', '-0.0228', '-0.005936', '0.012085', '0.003202', '-0.03006', '-0.03522', '0.02687', '-0.00509', '-0.04395', '-0.000211', '0.03354', '0.02332', '0.007286', '0.004467', '-0.01143', '0.004417', '0.063', '0.05518', '-0.06174', '0.0521', '-0.0427', '0.0202', '-0.00607', '-0.0235', '0.007576', '0.01787', '0.03326', '-0.01894', '-0.06134', '-0.03815', '-0.01416', '-0.00206', '-0.0003812', '0.04843', '-0.01053', '0.000456', '0.02779', '0.05145', '0.05527', '0.01518', '0.02153', '0.0422', '0.001111', '0.0208', '0.123', '0.02016', '0.0644', '-0.0802', '-0.00574', '0.02414']",,,C565882,,,,
mondo:0008914,cardioauditory syndrome of Sanchez Cascos,"['Sanchez Cascos cardioauditory syndrome', 'cardioauditory syndrome of Sanchez Cascos']",,212100,,C1859329,,,,C535577,,,,
mondo:0008915,dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome,"['dilated cardiomyopathy with hypergonadotropic hypogonadism', 'cardiomyopathy, dilated, with hypergonadotropic hypogonadism', 'genital anomaly with cardiomyopathy', 'Malouf syndrome', 'cardiogenital syndrome', 'cardiomyopathy with primary testicular failure', 'cardiomyopathy, dilated, with premature ovarian failure', 'cardiomyopathy, congestive, with hypergonadotropic hypogonadism', 'Najjar syndrome']",0111584,212112,2229,C0796083,"['0.2837', '-0.5234', '-0.1595', '0.3523', '-0.1178', '-0.575', '0.5737', '0.8774', '-0.273', '-0.5767', '0.3591', '-0.528', '-0.1631', '0.1186', '-0.7134', '0.3674', '-0.5854', '0.1118', '-0.7773', '-0.7134', '0.352', '0.57', '0.57', '-0.2458', '0.525', '-0.3257', '0.1353', '0.3896', '-0.0656', '-0.5435', '0.766', '-0.2542', '0.6187', '0.322', '0.3286', '-0.7617', '-0.11554', '-0.678', '0.79', '-0.509', '0.2142', '0.7124', '-0.1242', '0.3984', '0.63', '0.4128', '0.496', '0.8135', '0.386', '-0.696', '-0.3416', '0.1554', '0.4827', '-0.1777', '0.562', '-0.5044', '-0.5386', '0.2253', '-0.645', '0.103', '-0.1333', '0.4841', '0.3098', '-1.054', '-0.978', '0.0849', '-0.11066', '0.5596', '-0.8125', '-0.2025', '-0.5425', '0.52', '0.09235', '-0.1718', '-0.02888', '0.6255', '-0.1982', '-0.3086', '-0.2778', '0.3708', '0.0913', '-0.3274', '-0.263', '-0.2468', '1.176', '-0.1956', '0.2217', '-0.00831', '0.5874', '0.303', '0.3652', '0.2083', '0.046', '0.3865', '1.102', '0.769', '0.03363', '-0.518', '-0.1774', '-0.4854']",C174217,,,,,,
mondo:0008916,cardiomyopathy associated with myopathy and sudden death,['cardiomyopathy associated with myopathy and sudden death'],,212130,,C1859328,,,,C565881,,,,
mondo:0008917,heart defects-limb shortening syndrome,"['cardioskeletal syndrome, KUWAITI type', 'heart defects and limb shortening']",,212135,1354,C1859327,,,,C535850,,,,
mondo:0008918,carnitine-acylcarnitine translocase deficiency,"['Cact deficiency', 'CACT deficiency', 'CARNITINE-acylcarnitine translocase deficiency', 'carnitine-acylcarnitine translocase deficiency', 'CACTD']",0111585,212138,159,C0342791,"['0.0627', '0.1831', '-0.445', '0.1287', '-0.2299', '-0.4368', '0.1793', '0.4355', '-0.084', '-0.4175', '-0.2922', '-0.3352', '0.278', '0.10895', '-0.75', '-0.4995', '-0.3938', '0.1859', '-0.588', '-1.2705', '0.4395', '-0.338', '0.6675', '-0.2108', '-0.555', '-0.6694', '-0.297', '-0.3096', '-0.01888', '-0.4172', '0.7188', '0.0557', '0.05573', '0.1787', '-0.9307', '-0.2783', '-0.2126', '-0.2429', '-0.532', '0.1514', '-0.03108', '-0.782', '0.1345', '0.11505', '-0.2883', '-0.1531', '-0.1797', '0.01022', '-0.2054', '0.64', '-0.07916', '0.03745', '0.1917', '-0.0909', '0.3381', '-0.4136', '0.7075', '0.0998', '0.2292', '0.7056', '0.2328', '0.3477', '0.3892', '-0.0625', '-0.4343', '0.1833', '0.02869', '0.4172', '-0.9375', '-0.4187', '-0.1708', '0.4077', '0.2715', '0.1012', '0.0337', '0.647', '-0.0645', '-0.3728', '-0.0865', '0.1293', '0.4602', '0.2578', '0.1108', '-0.2524', '0.2827', '0.902', '-0.2715', '0.001299', '0.796', '-0.5493', '0.343', '0.3857', '-0.2052', '-0.03087', '-0.0546', '0.85', '0.4656', '-0.01119', '-0.3252', '0.04404']",C133086,,C562812,,,,
mondo:0008919,systemic primary carnitine deficiency disease,"['carnitine uptake defect', 'CDSP', 'Carnitine deficiency, systemic, due to defect in renal reabsorption of carnitine', 'Carnitine transporter defect', 'deficiency of plasma-membrane carnitine transporter', 'carnitine transporter deficiency', 'Carnitine deficiency, primary', 'Carnitine deficiency', 'systemic Carnitine deficiency', 'CARNITINE deficiency, systemic primary', 'Carnitine uptake deficiency', 'renal carnitine transport defect', 'Carnitine deficiency, systemic, due to defect in renal reabsorption of Carnitine', 'primary carnitine deficiency', 'Carnitine plasma-membrane transporter deficiency', 'cud', 'SPCD', 'systemic primary carnitine deficiency', 'Carnitine transporter, plasma-Membrane, deficiency of', 'Carnitine uptake defect']",14365,212140,158,C0342788,"['0.05173', '-0.0862', '-0.3372', '-0.2283', '0.1736', '-0.3362', '0.2152', '0.6924', '0.225', '-0.02394', '-0.6787', '-0.27', '0.0734', '0.02242', '-0.3552', '0.099', '-0.5654', '-0.4343', '-0.8213', '-0.731', '-0.216', '-0.8486', '0.7554', '-0.5093', '-0.1812', '-0.3335', '-0.08484', '0.1848', '-0.4421', '-0.1688', '0.5557', '0.04996', '0.358', '-0.2517', '-0.611', '0.3247', '0.01924', '0.1018', '-0.2588', '0.1191', '0.06247', '-0.281', '0.4446', '-0.02782', '-0.01804', '-0.5293', '0.03662', '-0.3792', '0.1995', '0.6797', '-0.02397', '-0.06683', '0.3904', '-0.3623', '0.595', '-0.262', '0.292', '0.12177', '-0.2432', '0.1948', '-0.1423', '0.1649', '0.2527', '-0.2896', '-0.29', '-0.339', '0.4202', '0.296', '-0.7427', '0.1199', '-0.2573', '-0.3167', '-0.3086', '0.2961', '-0.1628', '0.2029', '0.2769', '0.1394', '0.0882', '-0.2352', '0.592', '-0.11896', '-0.1375', '-0.534', '0.6973', '0.1211', '0.1685', '-0.1685', '0.7236', '-0.1172', '0.1367', '0.1512', '0.1672', '-0.3103', '0.5034', '0.5444', '0.2625', '-0.1743', '-0.611', '-0.383']",C98864,,C536778,277.82,,,
mondo:0008920,"carnitine deficiency, myopathic","['carnitine deficiency, myopathic', 'myopathic carnitine deficiency']",,212160,,C1859318,,,,C536100,,,,
mondo:0008921,carnosinemia,"['Carnosinase deficiency', 'carnosinemia', 'homocarnosinosis']",,212200,1361,C3495555,,C125661,,,,,,
mondo:0008922,Sengers syndrome,"['cardiomyopathy and cataract', 'mitochondrial DNA depletion syndrome 10 (Cardiomyopathic type)', 'cardiomyopathic mitochondrial DNA depletion syndrome 10', 'Sengers syndrome', 'congenital cataract-hypertrophic cardiomyopathy-mitochondrial myopathy syndrome', 'mitochondrial DNA depletion syndrome 10', 'cataract and cardiomyopathy']",0080132,212350,1369,C1859317,"['-0.6377', '0.4424', '-0.3494', '-0.1395', '-0.001623', '-0.4592', '0.1427', '1.708', '-0.849', '-0.06506', '-0.10077', '-0.6104', '0.01671', '-0.1137', '-0.274', '0.1996', '0.3618', '-0.1677', '-0.851', '-1.121', '-0.2917', '-0.12286', '0.0219', '0.2157', '0.0703', '-0.158', '-0.8027', '0.5537', '-0.158', '-0.0701', '0.4863', '0.1718', '1.229', '0.162', '0.241', '-0.3845', '-0.09546', '-0.666', '-0.006878', '0.4944', '-0.2769', '-0.04202', '0.5146', '0.595', '-0.2329', '0.7446', '-0.3289', '-0.2559', '0.4697', '0.1917', '-0.206', '-0.4612', '0.02773', '-0.1224', '-0.039', '-1.081', '0.2944', '-0.41', '0.023', '0.2512', '0.3916', '-0.4446', '0.6772', '0.5957', '-0.599', '-0.0806', '0.8223', '0.599', '-0.1777', '0.44', '-0.0844', '-0.07336', '0.318', '-0.2256', '0.712', '-0.046', '0.1608', '-0.4263', '-0.725', '1.27', '0.2607', '-0.09753', '0.03717', '-0.1925', '-0.0627', '0.2598', '0.586', '0.1384', '0.295', '0.313', '0.6064', '-0.08673', '0.0229', '0.395', '0.2764', '0.2084', '0.4236', '-0.2101', '-0.02354', '-0.445']",,,C538280,,,,
mondo:0008923,autosomal recessive palmoplantar keratoderma and congenital alopecia,"['autosomal recessive palmoplantar hyperkeratosis and congenital alopecia', 'PPK-CA, Wallis type', 'PPKCA2', 'cataract, alopecia, sclerodactyly', 'cass', 'palmoplantar keratoderma and congenital alopecia 2', 'palmoplantar keratoderma and congenital alopecia, Wallis type', 'Ppkca, Wallis type', 'cataract, alopecia, sclerodactyly syndrome', 'palmoplantar keratoderma and congenital alopecia type 2', 'cataract-alopecia-sclerodactyly syndrome']",0111245,212360,1366,C1859316,,,,C535336,,,,
mondo:0008924,congenital cataract-ichthyosis syndrome,"['cataract and congenital ichthyosis', 'Syndermotic cataract and congenital ichthyosis']",,212400,1376,C1859315,,,,C538281,,,,
mondo:0008925,cataract 46 juvenile-onset,"['CTRCT46', 'cataract, congenital or juvenile', 'early-onset non-syndromic cataract caused by mutation in LEMD2', 'cataract Hutterite type', 'cataract, juvenile, Hutterite type', 'LEMD2 early-onset non-syndromic cataract', 'cataract 46, juvenile-onset', 'juvenilae cataract Hutterite type']",0110243,212500,98987,,"['-0.3022', '0.1298', '-0.04785', '0.2986', '0.07336', '-0.2976', '-0.06476', '0.4316', '-0.384', '-0.2368', '-0.03162', '-0.2244', '-0.1708', '0.2383', '-0.03001', '-0.2411', '0.08716', '-0.11755', '0.0803', '-0.468', '0.10895', '-0.03363', '0.0727', '-0.11664', '0.0809', '0.0592', '-0.01516', '0.1383', '-0.002655', '0.1969', '0.1221', '-0.1742', '0.1509', '0.26', '0.07526', '0.03326', '0.1747', '-0.1997', '-0.04395', '-0.2515', '0.3203', '-0.2015', '-0.010605', '0.197', '-0.1616', '-0.2622', '0.0779', '-0.1141', '0.2257', '-0.01984', '0.22', '-0.04962', '0.12164', '0.0345', '-0.06195', '-0.3118', '0.57', '0.02286', '-0.2847', '-0.00833', '0.2184', '-0.0724', '0.1495', '0.06058', '-0.1621', '0.2754', '0.3699', '0.253', '0.006485', '0.10504', '-0.3687', '0.14', '0.1936', '0.01672', '0.04666', '0.08246', '0.06155', '0.1182', '-0.3462', '0.04303', '-0.1703', '0.1028', '-0.164', '0.1592', '0.1111', '-0.3438', '0.2698', '0.2812', '0.1879', '0.2864', '0.2166', '0.2112', '0.091', '-0.1361', '0.322', '-0.1549', '0.4011', '-0.332', '0.1313', '-0.05856']",,,C538286,,,,
mondo:0008926,COFS syndrome,"['Pena-Shokeir syndrome type 2', 'cerebrooculofacioskeletal syndrome', 'cerebro-oculo-facio-skeletal syndrome', 'COFS']",0080910,,1466,C0220722,"['-0.2703', '0.5317', '-0.01884', '-0.1769', '0.2944', '-0.5117', '0.5127', '0.3943', '-0.618', '-0.158', '0.3215', '-0.1699', '-0.187', '-0.1847', '-0.11536', '0.6113', '-0.014534', '-0.05634', '0.0693', '-0.564', '0.4438', '-0.03723', '0.03017', '-0.471', '-0.3594', '0.585', '-0.0875', '0.303', '-0.0638', '0.08563', '0.1918', '0.534', '0.43', '0.0268', '-0.1242', '0.3003', '-0.1392', '-0.3867', '-0.6045', '-0.1011', '0.384', '-0.4016', '0.1241', '-0.1761', '-0.0961', '-0.6245', '-0.02693', '0.03098', '0.2474', '-0.1501', '-0.2026', '-0.5176', '-0.2788', '-0.4846', '0.006466', '-0.4', '0.4558', '0.1544', '-0.04977', '0.0923', '0.008865', '-0.2252', '0.476', '0.3123', '-0.1002', '-0.198', '0.1895', '0.51', '-0.316', '0.3044', '-0.4902', '0.5596', '-0.05402', '0.363', '0.3262', '0.4834', '0.02281', '0.11334', '-0.3826', '-0.225', '-0.1599', '0.2065', '-0.5356', '0.7495', '-0.2026', '0.0929', '0.889', '0.489', '-0.1848', '-0.1699', '0.881', '0.1598', '-0.07184', '0.3079', '0.3203', '0.27', '0.1034', '-0.409', '0.7065', '0.0591']",C3817,,,,,,
mondo:0008927,colobomatous optic disc-macular atrophy-chorioretinopathy syndrome,"['ODRMD', 'optic DISC anomalies with retinal and/or macular dystrophy']",0080635,212550,435930,CN237578,,,,C565876,,,,
mondo:0008928,cataract-ataxia-deafness syndrome,"['cataract-ataxia-deafness-retardation syndrome', 'polyneuropathy-cataract-deafness syndrome', 'cataract ataxia deafness', 'Begeer syndrome', 'cataract ataxia deafness syndrome', 'polyneuropathy, cataract, deafness syndrome']",,212710,1368,C0796123,,,,C538283,,,,
mondo:0008930,"celiac disease, susceptibility to, 1","['celiac sprue, susceptibility to, 1', 'CELIAC1', 'gluten-sensitive enteropathy, susceptibility to, 1', 'coeliac disease, susceptibility to, type 1', 'celiac disease, susceptibility to', 'coeliac disease, susceptibility to', 'celiac disease, susceptibility to, 1', 'coeliac sprue, susceptibility to, 1', 'susceptibility to celiac disease 1', 'susceptibility to coeliac disease 1', 'celiac disease, susceptibility to, type 1']",,212750,,,,,,,,,,
mondo:0008931,Cenani-Lenz syndactyly syndrome,"['Cenani-Lenz type syndactyly', 'syndactyly, type 7', 'Cenani syndactylism', 'CLSS', 'Cenani syndactyly', 'Cenani-Lenz syndactyly syndrome', 'syndactyly Cenani Lenz type', 'Cenani-Lenz syndactyly', 'Cenani-Lenz syndrome', 'syndactyly type 7']",0090015,212780,3258,C1859309,"['-0.328', '-0.12445', '0.004032', '-0.3853', '0.1315', '-0.0235', '0.1797', '0.709', '-0.4805', '-0.6606', '0.3208', '-0.4585', '0.2107', '0.465', '-0.03079', '0.08435', '0.4133', '-0.1466', '-0.346', '-0.0699', '-0.0637', '0.36', '0.5806', '-0.291', '0.011185', '0.0863', '-0.1298', '0.06125', '0.2957', '0.0485', '0.082', '-0.2169', '0.1586', '0.1534', '0.3584', '-0.45', '-0.00495', '-0.2673', '-0.1499', '-0.1401', '0.271', '-0.5864', '0.285', '-0.565', '0.694', '-0.3206', '-0.1676', '0.536', '-0.6157', '-0.264', '0.07227', '-0.4526', '-0.0702', '0.4033', '-1.021', '-0.5806', '-0.2861', '-0.1587', '0.03278', '-0.05505', '0.238', '-0.1198', '0.1293', '0.2177', '-0.5054', '-0.1282', '0.0256', '0.2089', '-0.2903', '0.6855', '-0.3013', '0.2568', '0.7896', '0.01651', '-0.0704', '0.793', '0.1278', '-0.1311', '-0.1858', '-0.13', '-0.2588', '-0.0398', '0.5054', '1.102', '0.2042', '0.5146', '-0.2766', '0.623', '0.03035', '-0.305', '-0.2241', '0.006966', '-0.204', '0.1182', '0.3657', '-0.1952', '0.3582', '-1.173', '0.5044', '0.5044']",,,C538150,,,,
mondo:0008932,premature centromere division,"['PCD', 'premature centromere division', 'X-chromosome centromere peculiarity']",,212790,,C1859308,,,,,,,,
mondo:0008933,cephalin lipidosis,['cephalin lipidosis'],,212800,,C1859307,,,,C565872,,,,
mondo:0008934,cerebellar ataxia-ectodermal dysplasia syndrome,"['cerebellar ataxia ectodermal dysplasia', 'cerebellar ataxia - ectodermal dysplasia', 'ectodermal dysplasia and cerebellar ataxia', 'cerebellar ataxia and ectodermal dysplasia']",,212835,1174,C1859306,,,,C535350,,,,
mondo:0008935,cerebellar ataxia-hypogonadism syndrome,"['Gordon-Holmes syndrome', 'luteinizing hormone-releasing hormone, deficiency of, with ataxia', 'cerebellar ataxia and hypogonadotropic hypogonadism', 'luteinizing hormone releasing hormone, deficiency of with ataxia', 'luteinizing hormone-releasing hormone deficiency with ataxia', 'Gordon Holmes syndrome', 'LHRH deficiency and ataxia', 'GDHS', 'cerebellar ataxia - hypogonadism']",0111587,212840,1173,C1859305,"['-0.2942', '-0.4175', '-0.00926', '-0.00852', '-0.1405', '-0.86', '0.0712', '-0.0866', '-0.488', '-0.841', '-0.04105', '0.1061', '-0.2173', '0.2313', '0.5674', '-0.3955', '-0.03342', '-0.1318', '-0.1069', '-1.047', '-0.1138', '-0.3174', '0.2363', '-0.7676', '0.4775', '-0.2688', '-0.2347', '0.1586', '0.065', '-1.051', '-0.003714', '0.4524', '-0.642', '-0.185', '0.299', '0.1958', '-0.1119', '0.2123', '0.2131', '0.1809', '0.207', '0.2097', '-0.4067', '0.4868', '0.6484', '-0.7754', '-0.00924', '0.418', '0.3115', '0.1035', '0.1487', '0.22', '-0.313', '-0.4893', '0.01345', '-0.923', '0.3867', '0.3328', '-0.07294', '0.582', '-0.51', '0.4475', '0.3687', '-0.0695', '-0.3616', '0.662', '0.354', '0.832', '-0.6304', '0.3586', '0.7085', '0.431', '0.1521', '-0.4958', '1.08', '0.2462', '0.2095', '0.0936', '0.009605', '0.3997', '-0.1573', '-0.8125', '0.10614', '0.891', '-0.3174', '-0.665', '0.2317', '-0.0919', '0.3977', '0.5337', '0.3667', '0.3723', '0.1741', '0.1171', '0.8433', '0.758', '0.297', '0.3726', '-0.3503', '0.0725']",,,C565870,,,,
mondo:0008936,cerebellar ataxia and neurosensory deafness,['cerebellar ataxia and neurosensory deafness'],,212850,,C1859304,,,,C565869,,,,
mondo:0008937,"cerebellar ataxia, benign, with thermoanalgesia","['cerebellar ataxia with loss of pain and temperature sensation', 'cerebellar ataxia, benign, with thermoanalgesia']",,212890,,C1859303,,,,C565868,,,,
mondo:0008938,early-onset cerebellar ataxia with retained tendon reflexes,"['EOCARR', 'cerebellar ataxia, early-onset, with retained tendon reflexes', 'EOCA', 'ataxia, harding type', 'cerebellar ataxia early onset with retained tendon reflex', 'Harding ataxia']",,212895,1177,C0393520,,,,C535633,334.3,,,
mondo:0008939,isolated cerebellar hypoplasia/agenesis,"['cerebellar hypoplasia', 'cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay', 'near total absence of cerebellum', 'congenital cerebellar Hypoplasia', 'isolated cerebellar agenesis', 'Chiari IV malformation', 'Chiari 4 malformation', 'subtotal absence of cerebellum']",0070338,213000,2246,,,C98890,,C562568,,,10008033,
mondo:0008941,hepatic fibrosis-renal cysts-intellectual disability syndrome,"['Thompson-Baraitser syndrome', 'cerebellar vermis aplasia with associated features suggesting SMITH-Lemli-Opitz syndrome and Meckel syndrome', 'Thompson Baraitser syndrome']",,213010,2031,,,,,C565867,,,,
mondo:0008943,autosomal recessive spinocerebellar ataxia 2,"['spinocerebellar ataxia, autosomal recessive 2', 'cerebelloparenchymal disorder 3', 'CPD 3', 'PMPCA autosomal recessive congenital cerebellar ataxia', 'cerebellar granular cell hypoplasia and intellectual disability, congenital', 'SCAR2', 'autosomal recessive congenital cerebellar ataxia caused by mutation in PMPCA', 'autosomal recessive spinocerebellar ataxia type 2', 'cerebellar hypoplasia, nonprogressive Norman type', 'CPDIII', 'autosomal recessive cerebelloparenchymal disorder type 3', 'cerebellar granular cell hypoplasia and mental retardation, congenital', 'CPD3']",0080061,213200,1170,C1859298,"['-0.1531', '-0.276', '-0.01721', '0.1174', '-0.1252', '-0.8076', '0.1147', '-0.03745', '-0.4656', '-0.793', '-0.1902', '0.08203', '0.0971', '-0.04156', '0.5537', '-0.2433', '-0.0634', '-0.1621', '0.05243', '-0.9644', '0.01987', '-0.3132', '0.3389', '-0.684', '0.4517', '-0.45', '-0.3433', '0.252', '-0.0846', '-0.872', '0.1559', '0.4463', '-0.5127', '-0.2089', '0.2996', '0.05554', '-0.09283', '0.05637', '0.436', '0.1807', '0.1543', '0.07764', '-0.382', '0.3635', '0.673', '-0.5625', '0.1401', '0.3325', '0.1812', '-0.1323', '-0.1151', '0.06647', '-0.2417', '-0.28', '0.01988', '-0.7344', '0.2046', '0.4487', '-0.01933', '0.4426', '-0.359', '0.1223', '0.272', '-0.0317', '-0.4402', '0.3657', '0.3389', '0.5117', '-0.402', '0.3933', '0.681', '0.492', '-0.09753', '-0.5654', '0.5396', '0.2898', '0.3508', '0.1407', '0.0967', '0.4739', '-0.3499', '-0.5703', '0.1995', '0.606', '-0.4426', '-0.502', '0.2225', '0.09076', '0.4075', '0.3896', '0.3496', '0.4856', '-0.0684', '0.072', '0.863', '0.676', '0.406', '0.3', '-0.10895', '0.05734']",,,C565865,,,,
mondo:0008944,Joubert syndrome 1,"['Joubert syndrome type 1', 'CORS1', 'Joubert syndrome 1', 'CPD4', 'cerebellooculorenal syndrome 1', 'Joubert-Boltshauser syndrome', 'cerebelloparenchymal disorder 4', 'Cerebellooculorenal syndrome 1', 'INPP5E Joubert syndrome', 'JBTS1', 'Joubert syndrome', 'Joubert syndrome caused by mutation in INPP5E']",0110980,213300,,CN119531,,,,,,,,
mondo:0008945,myoclonic cerebellar dyssynergia,"['cerebelloparenchymal disorder 5', 'dentatorubral atrophy', 'Ramsay Hunt syndrome type 1 (formerly)', 'dentate cerebellar ataxia', 'Ramsay Hunt syndrome', 'progressive cerebellar tremor', 'CPD5', 'Ramsay Hunt syndrome type 1', 'Spinodentate atrophy', 'dyssynergia cerebellaris progressiva', 'cerebelloparenchymal disorder type 5', 'primary dentatum atrophy', 'progressive myoclonus ataxia', 'cerebelloparenchymal disorder V', 'dyssynergia cerebellaris myoclonica of Hunt', 'myoclonus and ataxia', 'dyssynergia cerebellaris myoclonica', 'Ramsay Hunt cerebellar syndrome']",12707,213400,,C1834580,,,1001053,D002527,,,,
mondo:0008946,"cerebral angiopathy, dysphoric","['cerebral angiopathy, dysphoric']",,213500,,C1859283,,,,C565864,,,,
mondo:0008947,bilateral striopallidodentate calcinosis,"['Fahr disease', 'cerebrovascular ferrocalcinosis', 'PFBC', 'idiopathic basal ganglia calcification', 'BSPDC', 'primary familial brain calcification', 'basal ganglia calcification', 'basal ganglia calcification, idiopathic']",0060230,,1980,CN852731,"['-0.3174', '0.503', '-0.04523', '-0.3608', '-0.1993', '-0.816', '-0.152', '0.223', '-0.802', '0.347', '-0.2134', '-0.4353', '-0.2654', '-0.2103', '0.648', '0.436', '0.02798', '-0.3699', '-0.2096', '-0.3643', '-0.1131', '-0.462', '-0.02548', '-0.1716', '0.4482', '0.1151', '0.2888', '-0.0636', '-0.464', '-0.1523', '0.347', '-0.2874', '0.1312', '-0.512', '-0.103', '0.216', '0.166', '-0.5625', '0.1401', '0.09955', '0.509', '-0.731', '0.2932', '0.297', '1.186', '-0.739', '-0.0907', '0.0733', '-0.2084', '0.487', '0.0673', '0.3066', '-0.1643', '-0.137', '0.173', '0.1387', '0.616', '-0.2825', '-0.3162', '0.0706', '0.04178', '0.1969', '-0.03662', '-0.544', '-0.4607', '0.02983', '0.04272', '0.2883', '-0.3176', '0.4517', '-0.0752', '-0.4246', '-0.2166', '-0.0913', '-0.01619', '0.2703', '0.3477', '0.1798', '-0.108', '0.1223', '0.3787', '-0.464', '0.5454', '0.1599', '0.0724', '0.007534', '0.0662', '-0.001116', '0.2952', '-0.1482', '-0.1447', '0.037', '0.1262', '0.00823', '0.534', '0.0727', '0.3977', '-0.0986', '-0.0675', '0.01883']",,,C536275,348.89,,10059626,0002135
mondo:0008948,cerebrotendinous xanthomatosis,"['cerebrotendinous xanthomatosis', 'cerebral cholesterinosis', 'sterol 27-hydroxylase deficiency', 'CTx', 'cholestanol storage disease']",4810,213700,909,C0238052,"['-0.2169', '0.1531', '-0.1202', '-0.523', '-0.3357', '-0.004997', '-0.1622', '0.765', '-0.9097', '0.05167', '-0.5547', '0.04526', '-0.1098', '0.328', '-0.03165', '-0.7095', '-0.2212', '-0.758', '-0.355', '-0.5596', '-0.04486', '-0.09283', '0.03625', '0.2043', '0.2135', '-0.1937', '0.1161', '-0.0885', '-0.4055', '-0.3157', '0.2961', '-0.4011', '0.201', '-0.1744', '-0.2595', '-0.1527', '-0.3608', '-0.5156', '-0.03568', '0.5356', '0.3792', '-0.259', '-0.0819', '0.727', '0.10974', '0.03256', '0.4497', '-0.05307', '-0.1984', '-0.1631', '0.1418', '0.7217', '-0.00514', '-0.584', '-0.1918', '0.1545', '1.217', '-0.3008', '-0.3616', '0.1699', '0.3054', '0.5557', '0.3215', '-0.395', '0.02438', '0.594', '0.4226', '0.01729', '0.1633', '-0.03165', '-0.4263', '0.00967', '-0.633', '0.1914', '0.4392', '0.509', '-0.015594', '-0.2444', '-0.631', '0.06415', '0.07306', '-0.181', '-0.01179', '0.2098', '0.1669', '0.5986', '-0.215', '-0.0049', '0.1827', '-0.2012', '0.1216', '0.637', '0.0851', '0.335', '0.4312', '-0.2874', '0.3958', '0.074', '-0.03882', '0.3882']",C84628,,D019294,,,,
mondo:0008949,"cerebral malformation, seizures, hypertrichosis, and overlapping fingers","['cerebral malformation, seizures, hypertrichosis, and overlapping fingers', 'Muller Barth Menger syndrome']",,213820,,C1859259,,,,C537370,,,,
mondo:0008950,cerebral sclerosis similar to Pelizaeus-Merzbacher disease,['cerebral sclerosis similar to Pelizaeus-Merzbacher disease'],,213900,,,,,,C536318,,,,
mondo:0008951,cerebrocortical degeneration of infancy,['cerebrocortical degeneration of infancy'],,213950,,C1859257,,,,C565863,,,,
mondo:0008953,peroxisome biogenesis disorder 1A (Zellweger),"['peroxisome biogenesis disorder, complementation group E', 'peroxisome biogenesis disorder 1A (Zellweger)', 'Zs', 'peroxisome biogenesis disorder, complementation group 1', 'PBD1A', 'Cerebrohepatorenal syndrome']",0080476,214100,,,,,,,,,,
mondo:0008954,peroxisome biogenesis disorder 2A (Zellweger),"['peroxisome biogenesis disorder, complementation group 2', 'PBD2A', 'peroxisome biogenesis disorder 2A (Zellweger)']",0080477,214110,,C3550273,,,,,,,,
mondo:0008955,cerebrooculofacioskeletal syndrome 1,"['ERCC6 COFS syndrome', 'COFS1', 'cerebrooculofacioskeletal syndrome 1', 'cerebrooculofacioskeletal syndrome type 1', 'COFS syndrome', 'COFS syndrome caused by mutation in ERCC6', 'Pena-Shokeir syndrome, type 2']",0080911,214150,,,,C173085,,,,,,
mondo:0008957,"cervical vertebrae, agenesis of","['cervical vertebrae, agenesis of']",,214290,,,,,,C562952,,,,
mondo:0008958,"Klippel-Feil syndrome 2, autosomal recessive","['Klippel-Feil syndrome 2, autosomal recessive', 'Kfs, autosomal recessive', 'MEOX1 isolated Klippel-Feil syndrome', 'KFS2', 'cervical vertebral fusion, autosomal recessive', 'isolated Klippel-Feil syndrome caused by mutation in MEOX1', 'Klippel-FEIL syndrome 2, autosomal recessive']",0080590,214300,,C1859209,,,,C536888,,,,
mondo:0008959,CHAND syndrome,"['CHAND syndrome', 'curly hair-ankyloblepharon-nail dysplasia syndrome', 'CHANDS']",,214350,1401,CN199447,"['-0.01035', '0.02147', '-0.00656', '0.001991', '-0.00411', '-0.01839', '-0.011154', '0.02525', '-0.01656', '-0.01668', '0.007313', '-0.007645', '-0.001808', '0.001957', '-0.0004182', '0.0002239', '-0.00895', '-0.007156', '0.001713', '-0.02014', '-0.007416', '-0.0114', '0.0127', '-0.01811', '0.01107', '-0.003773', '-0.01828', '-0.010056', '0.0126', '-0.013306', '0.01591', '-0.00852', '0.02652', '0.011185', '-0.004135', '-0.01124', '0.004032', '-0.00284', '-0.00493', '-0.013756', '0.012146', '-0.02213', '-0.00652', '-0.001073', '-0.005516', '-0.01479', '-0.004322', '0.01005', '0.007133', '0.009865', '-0.002708', '0.005714', '0.006794', '0.00217', '-0.001531', '-0.006638', '0.012726', '-0.008705', '-0.007458', '0.00553', '0.01602', '-0.001813', '0.005085', '-0.005024', '-0.00592', '0.01012', '0.003595', '-0.001143', '-0.01994', '0.01631', '-0.02588', '0.000615', '0.00738', '-0.0178', '0.007736', '0.01483', '-0.01011', '-0.005', '-0.01932', '-0.01306', '0.00593', '0.00624', '-0.01417', '0.01633', '0.004944', '0.004887', '-0.003551', '0.02364', '0.01507', '-0.0073', '0.00565', '0.00493', '0.0002716', '0.006256', '0.02536', '0.002968', '0.003603', '-0.02919', '0.005695', '0.01244']",,,C538074,,,,
mondo:0008960,Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome,"['hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibers', 'Charcot-Marie-Tooth disease and deafness', 'Charcot-Marie-Tooth disease-hearing loss-intellectual disability syndrome', 'hereditary motor and sensory neuropathy with deafness, intellectual disability and absent sensory large myelinated fibres', 'neuropathy, hereditary motor and sensory, with deafness, intellectual disability, and absent sensory large myelinated fibres', 'Charcot-Marie-tooth disease-deafness-intellectual disability syndrome', 'deafness with Charcot-Marie-Tooth disease', 'neuropathy, hereditary motor and sensory, with deafness, intellectual disability, and absent sensory large myelinated fibers', 'neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibres', 'neuropathy, hereditary motor and sensory, with deafness, mental retardation, and absent sensory large myelinated fibers']",,214370,90103,,,,,,,,,
mondo:0008961,Charcot-Marie-Tooth disease type 4A,"['Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4A', 'Charcot-Marie-Tooth neuropathy, type 4A', 'autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4A', 'CMT4A', 'GDAP1 Charcot-Marie-Tooth disease type 4', 'Charcot-Marie-Tooth neuropathy type 4A', 'Charcot Marie Tooth disease type 4A', 'Charcot-Marie-Tooth disease, demyelinating, autosomal recessive', 'Charcot-Marie-Tooth disease type 4 caused by mutation in GDAP1', 'Charcot-Marie-Tooth disease, type 4A']",0110185,214400,99948,C1859198,"['0.00576', '0.473', '0.0878', '0.06274', '-0.03662', '-0.2673', '-0.1495', '0.6484', '-0.9233', '0.07135', '0.04886', '0.2976', '-0.33', '0.2144', '-0.3105', '-0.3838', '0.01546', '-0.4011', '-0.2106', '-0.574', '0.1233', '0.1691', '0.4165', '0.438', '0.3052', '0.5947', '-0.07184', '0.1783', '0.1276', '-0.2478', '-0.1378', '-0.5312', '-0.02628', '0.2747', '0.1472', '-0.756', '-0.5093', '-0.193', '0.4', '-0.2815', '-1.669', '-0.1682', '-0.4814', '0.8613', '-0.3442', '-0.3918', '0.0151', '0.0234', '-0.00634', '0.04926', '0.05624', '0.2727', '-0.496', '-0.9004', '0.2141', '-0.402', '-0.0494', '0.2515', '-0.3923', '0.011826', '-0.4443', '0.1365', '0.8315', '1.038', '-1.012', '1.012', '0.153', '1.029', '-0.6846', '0.625', '-0.7993', '0.0763', '0.4426', '-0.1472', '1.186', '0.3572', '-0.502', '0.5576', '0.1431', '-0.675', '-0.2786', '-0.117', '0.6895', '0.6006', '-0.1124', '-0.1284', '0.0802', '0.4695', '1.069', '0.2329', '0.332', '-0.11304', '0.1932', '0.528', '0.3184', '0.663', '0.636', '-0.4778', '-0.0498', '0.4717']",,,C535419,,,,
mondo:0008962,Griscelli syndrome type 1,"['Griscelli syndrome, type 1', 'Griscelli syndrome, cutaneous and neurologic type', 'Griscelli disease type 1', 'Griscelli syndrome with neurological impairment', 'Griscelli-PruniC)ras syndrome type 1', 'pigmentary dilution of the skin and hair, the presence of large clumps of pigment in hair shafts', 'Griscelli syndrome, cutaneous and neurological type', 'partial albinism and primary neurologic disease without hemophagocytic syndrome', 'Griscelli-Pruniéras syndrome type 1', 'GS1', 'hypopigmentation-neurologic impairment syndrome', 'Griscelli syndrome with neurologic impairment']",0060832,214450,79476,C1859194,"['-0.2174', '0.06885', '-0.04205', '0.0759', '0.516', '-0.2925', '-0.3538', '0.0869', '-0.301', '0.0664', '0.02866', '-0.0776', '-0.11383', '-0.0361', '0.03008', '-0.0871', '0.2622', '-0.1542', '-0.1598', '-0.476', '-0.05484', '-0.2034', '0.1825', '-0.03964', '0.01145', '0.01063', '-0.163', '0.1442', '-0.02718', '0.04953', '0.4995', '0.129', '0.0824', '-0.11743', '0.176', '0.04407', '-0.1708', '-0.0771', '0.0637', '-0.4016', '0.389', '-0.399', '0.01514', '-0.11127', '-0.2861', '-0.3237', '0.10986', '0.02237', '0.2964', '-0.11975', '-0.1837', '-0.1298', '0.2603', '0.2742', '-0.10986', '-0.1536', '0.4067', '0.0651', '-0.3254', '-0.1923', '-0.08594', '0.07916', '0.2861', '-0.03625', '0.2258', '0.163', '0.1842', '0.0738', '-0.4053', '0.34', '-0.5312', '-0.3', '-0.02803', '0.05045', '0.03745', '-0.205', '-0.006527', '0.1741', '0.0346', '-0.0737', '0.3606', '-0.3398', '-0.05783', '0.0555', '-0.1469', '-0.3198', '0.3196', '0.675', '0.3198', '0.3972', '0.1403', '0.3445', '0.2023', '-0.03108', '0.5146', '0.1428', '0.02657', '-0.4426', '0.12384', '0.291']",,,C537301,,E70.3,,
mondo:0008963,Chediak-Higashi syndrome,"['Chediak - Steinbrinck anomaly', 'ChC)diak-Higashi-Steinbrink syndrome', 'Chediak-Higashi syndrome', 'Chédiak-Higashi disease', 'Chédiak-Higashi-Steinbrink syndrome', 'Chediak Higashi syndrome', 'Chédiak-Higashi syndrome', 'CHS', 'ChC)diak-Higashi disease']",2935,214500,167,C0007965,"['0.1597', '0.4504', '-0.2274', '-0.4163', '0.04794', '0.1262', '-0.09564', '0.554', '0.424', '0.1216', '0.3206', '-0.1417', '-0.1373', '0.3901', '0.2144', '-0.2537', '0.5986', '-0.1771', '0.514', '-0.7583', '-0.2776', '-0.331', '0.6074', '-0.3672', '-0.2625', '0.07135', '-0.04803', '0.386', '-0.1802', '-0.1354', '-0.001403', '0.1175', '0.5054', '-0.05124', '0.1478', '0.1006', '-0.3577', '-0.7295', '0.1963', '-0.004196', '0.7075', '-0.573', '0.192', '-0.3442', '0.2847', '-0.3362', '-0.3547', '-0.4905', '0.1738', '-0.2122', '0.2913', '0.3086', '0.529', '0.202', '0.415', '0.1495', '0.5635', '-0.2107', '-0.2064', '0.1853', '-0.04425', '-0.03177', '0.282', '0.05005', '0.3577', '0.04263', '-0.1489', '-0.03506', '0.6343', '1.222', '-0.2896', '-0.5654', '0.0726', '-0.301', '0.5874', '-0.02316', '0.4175', '-0.3752', '0.427', '-0.0574', '-0.3635', '-0.1954', '0.1498', '0.6284', '-0.4565', '0.3843', '0.4377', '0.0674', '0.822', '0.2028', '0.92', '0.2085', '0.0562', '0.564', '0.4211', '0.4631', '0.04507', '-0.2062', '0.1296', '0.3433']",C2941,,D002609,,E70.330,10008415,
mondo:0008964,congenital secretory chloride diarrhea 1,"['congenital chloride diarrhoea', 'secretory diarrhoea caused by mutation in SLC26A3', 'chloride diarrhea, congenital, Finnish type', 'diarrhoea 1, secretory chloride, congenital', 'congenital chloride diarrhea', 'congenital secretory chloride diarrhea type 1', 'congenital chloride diarrhoea Finnish type', 'CLD', 'DIAR1', 'familial chloride diarrhoea', 'familial chloride diarrhea', 'congenital secretory chloride diarrhoea type 1', 'SLC26A3 secretory diarrhoea', 'SLC26A3 secretory diarrhea', 'congenital chloride diarrhea Finnish type', 'secretory diarrhea caused by mutation in SLC26A3', 'diarrhea 1, secretory chloride, congenital', 'Darrow-gamble disease', 'congenital chloridorrhea', 'Chloridorrhea, congenital']",0060296,214700,53689,,"['0.2615', '0.0745', '0.3848', '0.2515', '-0.507', '-0.9214', '-1.014', '0.3333', '-0.147', '0.0638', '0.635', '0.6333', '0.4854', '0.635', '-1.096', '0.0873', '-0.4749', '0.2487', '-0.612', '-0.8047', '-0.01607', '-0.0775', '-0.07477', '-0.037', '0.2245', '-0.7256', '-0.7124', '0.6255', '0.502', '-0.806', '-0.358', '-0.6147', '-0.05704', '0.4377', '0.83', '0.455', '-0.345', '0.5225', '0.2239', '-0.1993', '-0.7124', '-0.498', '-0.2378', '-0.612', '0.3657', '-0.1294', '-0.0564', '0.249', '0.1154', '1.28', '-0.753', '-0.141', '0.0892', '-0.2634', '-0.04788', '-0.4678', '-0.1749', '0.1512', '-0.4902', '0.0521', '0.376', '0.777', '0.4495', '-0.3381', '0.1114', '-0.08765', '0.2976', '-0.2632', '-0.002438', '0.9927', '-0.4036', '0.7915', '0.315', '-0.879', '0.646', '0.1411', '-0.6465', '0.009155', '-0.2205', '0.667', '-0.2124', '-0.614', '-0.1321', '0.1959', '0.4177', '0.3235', '0.574', '-0.03056', '0.08527', '-0.2527', '-0.09656', '-0.3184', '-0.307', '-0.4387', '0.606', '0.7236', '0.375', '-1.745', '-0.2559', '-0.2634']",,,C536210,579.8,,,
mondo:0008965,CHARGE syndrome,"['Hall-Hittner syndrome', 'coloboma, heart anomaly, choanal atresia, retardation, genital and ear anomalies', 'coloboma, heart defects, choanal atresia, retardation of Growth and development, genital abnormalities, and Ear anomalies association', 'coloboma, heart malformation, choanal atresia, retardation of Growth and development, genital abnormalities, and Ear malformations (CHARGE) association', 'CHARGE association', 'coloboma-heart defects-atresia choanae-retardation of growth and development-genitourinary problems-ear abnormalities syndrome', 'Charge association--coloboma, heart anomaly, choanal atresia, retardation, genital and Ear anomalies', 'CHARGE syndrome']",0050834,214800,138,C0265354,"['-0.2084', '0.684', '0.5054', '-0.734', '0.1597', '0.1177', '0.604', '0.804', '-0.76', '0.04672', '-0.10547', '-0.9385', '-0.3167', '-0.2015', '-0.304', '-0.1771', '-0.344', '-0.03372', '-0.904', '-0.1599', '0.226', '-0.2313', '0.3948', '0.04327', '-0.291', '0.0919', '-0.4453', '-0.1674', '0.6104', '-0.0796', '-0.00955', '0.454', '0.3713', '-0.1931', '-0.09705', '-0.3838', '0.0902', '-0.6436', '-0.8013', '-0.387', '-0.00179', '0.02013', '-0.02298', '0.2063', '0.6787', '-0.2252', '0.2133', '0.166', '-0.3232', '0.65', '-0.1868', '0.0769', '0.1263', '-0.4204', '-0.624', '0.1746', '0.11896', '-0.1332', '0.00394', '0.0893', '-0.5957', '0.468', '-0.0459', '0.684', '0.3708', '0.5254', '0.2173', '0.3662', '-0.2607', '0.1354', '0.2107', '-0.10034', '-0.1669', '-0.011734', '-0.09485', '-0.407', '0.4985', '-0.561', '-0.4495', '-0.3083', '0.1039', '-0.6895', '0.02151', '0.8', '-0.1862', '-0.4702', '0.6426', '0.3665', '0.2167', '0.372', '-0.1442', '0.46', '-0.04962', '0.1984', '0.4556', '-0.05707', '-0.05975', '-0.4014', '0.487', '0.3513']",C75100,,D058747,759.89,,10064063,
mondo:0008966,Aagenaes syndrome,"['lymphedema cholestasis syndrome', 'cholestasis lymphedema syndrome', 'LCS1', 'LCS', 'Aagenaes syndrome', 'cholestasis-lymphedema syndrome', 'lymphedema-cholestasis syndrome', 'Chls', 'cholestasis-edema syndrome, Norwegian type']",6691,214900,1414,C0268314,,C35709,,C535330,576.8,Q82.0,,
mondo:0008967,congenital bile acid synthesis defect 4,"['CBAS4', 'congenital bile acid synthesis defect 4', 'cholestasis, intrahepatic, with defective conversion of', '2-methylacyl-CoA racemase deficiency', 'Trihydroxycoprostanic acid to cholic acid', 'trihydroxycoprostanic acid in bile', 'bile acid synthesis defect, congenital, type 4', 'AMACR deficiency', 'bile acid synthesis defect, congenital, 4', 'cholestasis, intrahepatic, with defective conversion of Trihydroxycoprostanic acid to cholic acid', 'congenital bile acid synthesis defect type 4', 'Alpha-methyl-acyl-CoA racemase deficiency', 'BAS defect type 4', 'Trihydroxycoprostanic acid in bile', 'liver disease-retinitis pigmentosa-polyneuropathy-epilepsy syndrome', 'intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid', 'BASD4']",0111068,214950,79095,,"['0.12036', '0.0678', '-0.2253', '0.02084', '0.3008', '-0.1465', '-0.614', '0.3591', '-0.123', '0.1575', '-0.401', '-0.4568', '0.2244', '0.6216', '-0.5913', '-0.8027', '-0.11176', '-0.2585', '-0.3037', '-0.6646', '-0.2277', '-0.434', '1.087', '-0.05942', '-0.03818', '-0.347', '-0.1738', '0.2144', '-0.3225', '-0.6167', '0.419', '0.3088', '0.4133', '0.4067', '-0.3545', '-0.4863', '-0.513', '-0.4126', '-0.1428', '0.6523', '0.2466', '-0.604', '0.1255', '0.0757', '-0.2349', '-0.3845', '0.2825', '-0.0375', '-0.4316', '-0.5073', '-0.1508', '-0.1099', '0.1037', '-0.562', '-0.4878', '-0.4653', '-0.02184', '0.1161', '-0.285', '0.3503', '0.531', '0.1456', '0.683', '-0.2455', '0.3367', '0.5283', '0.245', '-0.2107', '-0.599', '-0.227', '0.1757', '0.105', '0.1199', '-0.11615', '0.256', '-0.2313', '0.1633', '-0.341', '-0.2443', '0.5854', '-0.11865', '-0.0895', '-0.4514', '0.11053', '-0.00525', '0.1877', '-0.1831', '0.1553', '0.764', '0.1101', '0.4104', '0.3909', '0.1697', '-0.2238', '0.8506', '0.3088', '0.3418', '-0.491', '-0.07275', '-0.0627']",,,C535444,,,,
mondo:0008968,"cholestasis with gallstone, ataxia, and visual disturbance","['cholestasis with gallstone, ataxia, and visual disturbance']",,214980,,C1859161,,,,C565856,,,,
mondo:0008969,cholesterol pneumonia,"['familiaere cholesterin-Pneumonie', 'cholesterol pneumonia']",,215030,,C0549472,,,,C535937,516.8,,,
mondo:0008970,chondrodysplasia Blomstrand type,"['Blomstrand type chondrodysplasia', 'chondrodysplasia, Blomstrand type', 'Blomstrand lethal osteochondrodysplasia', 'Blomstrand osteochondrodysplasia', 'Blomstrand lethal chondrodysplasia', 'Blomstrand^s lethal chondrodysplasia', 'Blomstrand chondrodysplasia', 'BOCD', 'BLC']",0060387,215045,50945,C1859148,"['-0.7446', '0.03873', '0.04984', '-0.1797', '0.2058', '0.1271', '-0.374', '0.698', '-0.7476', '-0.523', '-0.2854', '-0.09644', '-0.06198', '-0.3076', '-0.3652', '0.02142', '0.2954', '-0.0906', '-0.435', '-0.4062', '0.04398', '0.1547', '1.026', '-0.5396', '-0.267', '0.04727', '-0.02', '0.2327', '0.576', '-0.3608', '-0.2363', '0.05823', '0.08514', '-0.1697', '0.4097', '0.1383', '-0.0561', '-0.1931', '-0.11664', '-0.01749', '-0.1667', '-0.3223', '-0.01973', '-0.11896', '-0.0153', '-0.7153', '-0.05063', '0.9194', '0.4685', '0.1948', '0.353', '-0.528', '-0.1907', '-0.0981', '-0.806', '-0.913', '-0.05222', '-0.3743', '0.2656', '0.4365', '-0.1306', '0.1058', '-0.5415', '-0.3416', '0.3328', '-0.1287', '0.3142', '0.2866', '-0.5557', '0.1965', '-0.3086', '-0.04904', '0.482', '-0.3247', '-0.3555', '0.3118', '-0.09235', '0.2595', '0.1799', '0.05664', '0.2001', '0.2378', '0.2173', '-0.2098', '0.003944', '0.6406', '0.2219', '0.11237', '0.691', '0.2034', '-0.1871', '0.03357', '0.2391', '-0.0821', '1.114', '0.4094', '0.422', '-0.295', '0.396', '0.1776']",C131420,,C537914,,,,
mondo:0008971,chondrodysplasia calcificans Metaphysealis,['chondrodysplasia calcificans Metaphysealis'],,215050,,C1859147,,,,C565855,,,,
mondo:0008972,rhizomelic chondrodysplasia punctata type 1,"['Rcdp1', 'peroxisome biogenesis disorder 9', 'chondrodystrophia calcificans punctata', 'rhizomelic chondrodysplasia punctata caused by mutation in PEX7', 'rhizomelic chondrodysplasia punctata type 1', 'chondrodysplasia punctata, rhizomelic form', 'RCDP1', 'rhizomelic chondrodysplasia punctata, type 1', 'PEX7 rhizomelic chondrodysplasia punctata', 'Pbd9']",0110851,215100,309789,C1859133,"['-0.3438', '0.2386', '0.05356', '-0.7197', '0.2294', '-0.2358', '-0.2825', '0.2778', '-0.763', '-0.2744', '-0.03607', '-0.002876', '0.02414', '0.1147', '0.248', '-0.01461', '0.1501', '0.02475', '-0.4688', '-0.6353', '0.02657', '0.3206', '0.894', '0.06525', '0.3228', '0.1151', '-0.003805', '-0.4849', '0.1783', '-0.0427', '0.01027', '-0.04556', '0.05054', '0.36', '0.465', '0.0927', '-0.112', '0.0681', '-0.1382', '-0.2152', '0.0326', '-0.3806', '-0.1295', '0.3826', '-0.2998', '-0.593', '-0.07367', '-0.002796', '0.1948', '-0.1102', '0.1526', '-0.32', '0.0983', '-0.2189', '-0.1648', '-0.749', '0.2001', '0.0835', '0.2546', '0.2793', '0.1805', '-0.1967', '0.2218', '0.2942', '0.018', '-0.07697', '-0.066', '0.1737', '-0.443', '0.4492', '-0.1017', '0.01886', '-0.01723', '-0.11554', '0.2087', '0.4712', '-0.08276', '0.2864', '-0.448', '-0.3606', '0.01311', '0.00991', '0.2001', '0.3232', '-0.3894', '-0.0777', '0.1471', '0.1832', '0.304', '0.2222', '-0.1727', '-0.00869', '-0.004436', '0.0712', '0.4514', '0.6406', '0.2588', '-0.4849', '0.339', '0.04413']",,,,,,,
mondo:0008973,"chondrodysplasia punctata, Toriello type","['chondrodysplasia punctata syndrome', 'Toriello-Higgins-Miller syndrome']",,215105,79347,,,,,C565853,,,,
mondo:0008974,Greenberg dysplasia,"['hem skeletal dysplasia', 'hydrops-ectopic calcification-moth-eaten skeletal dysplasia', 'Greenberg dysplasia', 'hydrops-ectopic calcification-motheaten syndrome', 'hydrops, ectopic calcification, moth-eaten skeletal dysplasia', 'Greenberg skeletal dysplasia', 'GRBGD', 'hem', 'chondrodystrophy, hydropic and prenatally lethal type', 'autosomal recessive lethal chondrodystrophy with congenital hydrops', 'hem dysplasia', 'moth-eaten skeletal dysplasia', 'skeletal dysplasia, Greenberg type', 'hem/Greenberg dysplasia']",0111588,215140,1426,CN199524,"['-0.691', '0.262', '0.01444', '-0.4668', '0.1721', '-0.362', '-0.2018', '0.4424', '-0.3843', '-0.4353', '-0.3354', '-0.02454', '-0.09863', '0.1809', '-0.0674', '0.1559', '0.03268', '0.3923', '-0.489', '-1.065', '-0.2162', '0.1306', '1.12', '-0.7056', '0.000251', '-0.2021', '0.11505', '-0.011955', '0.724', '-0.3196', '-0.05383', '-0.2091', '0.2832', '0.267', '0.2341', '0.2001', '-0.3962', '-0.3193', '-0.00882', '0.2196', '-0.1923', '-0.2673', '0.1917', '0.11383', '-0.1798', '-0.3723', '-0.4832', '0.1124', '0.1804', '0.01688', '0.6626', '-0.3967', '0.1588', '0.4788', '-0.3196', '-1.047', '-0.0597', '-0.2219', '0.3052', '0.2015', '0.3906', '0.354', '-0.09125', '0.2118', '-0.2915', '-0.559', '0.329', '0.181', '-0.507', '0.229', '-0.314', '0.05548', '0.488', '0.0515', '-0.1814', '0.1567', '0.164', '0.1909', '-0.567', '-0.2964', '-0.04907', '0.4458', '0.4402', '0.4426', '0.0925', '0.329', '0.3086', '0.3152', '-0.05237', '-0.05527', '0.349', '0.01199', '0.05304', '0.2869', '0.6123', '0.4905', '0.824', '-0.3826', '0.514', '0.1466']",,,C535858,,,,
mondo:0008975,otospondylomegaepiphyseal dysplasia,"['Nance-Sweeney chondrodysplasia', 'Nance-Insley syndrome', 'Nance Sweeney chondrodysplasia', 'otospondylmegaepiphyseal dysplasia', 'Insley-Astley syndrome', 'OSMED syndrome', 'OSMED', 'chondrodystrophy with sensorineural deafness', 'otospondylomegaepiphyseal dysplasia', 'oto-spondylo-mega-epiphyseal dysplasia']",0080026,,1427,,"['-0.154', '-0.09357', '-0.1268', '0.1532', '0.4849', '-0.6235', '0.3171', '0.8354', '-0.534', '-0.297', '-0.273', '-0.1471', '0.2094', '-0.007263', '-0.472', '0.03072', '0.6016', '-0.1676', '-0.502', '-0.393', '-0.10254', '-0.2377', '0.2957', '-0.067', '0.0896', '0.1699', '-0.1604', '0.1364', '0.2439', '0.2251', '0.1159', '-0.12195', '-0.188', '-0.0512', '0.2471', '-0.2754', '0.2091', '-0.4165', '0.11786', '0.03186', '0.2898', '-0.2025', '0.137', '-0.02126', '-0.2109', '-0.0115', '0.0837', '0.3535', '-0.14', '-0.2957', '-0.1028', '-0.0637', '0.3337', '0.262', '0.1628', '-0.8335', '-0.01354', '-0.1962', '0.2421', '-0.2057', '0.364', '0.05838', '-0.4348', '-0.1316', '-0.144', '-0.117', '0.1682', '0.567', '-0.2654', '0.0812', '-0.2428', '0.03665', '0.2361', '-0.3503', '0.06525', '0.686', '-0.0981', '0.05066', '0.088', '0.02313', '0.2913', '-0.05374', '0.3027', '0.833', '-0.1497', '0.4497', '-0.366', '0.4216', '-0.05743', '0.1644', '0.2184', '0.511', '0.2742', '0.2024', '0.713', '0.1692', '0.5845', '-0.758', '0.6797', '0.2417']",,,,759.89,,,
mondo:0008976,"chondroitin-6-sulfaturia, defective cellular immunity, nephrotic syndrome","['chondroitin-6-Sulfaturia, defective cellular immunity, nephrotic syndrome']",,215250,,C1859104,,,,C565852,,,,
mondo:0008977,chondrosarcoma,"['chondrosarcoma, somatic mutation', 'chondrosarcoma (disease)', 'chondrosarcoma of bone', 'primary chondrosarcoma of the bone', 'chondrosarcoma, malignant', 'chondrosarcoma']",3371,215300,55880,C0008479,"['-0.2795', '-0.1125', '0.2925', '-0.1539', '0.2988', '-0.4495', '0.926', '0.08496', '-0.2369', '-0.4165', '0.2141', '0.571', '-0.387', '0.523', '-0.564', '0.01935', '-0.28', '-0.5854', '-0.04205', '-0.5137', '0.000889', '-0.3418', '0.4304', '-0.2324', '0.3025', '-0.3428', '0.302', '-0.5127', '-0.5835', '0.1315', '0.5073', '-0.1807', '0.4998', '-0.4019', '0.2185', '0.02301', '-0.7305', '0.5327', '-0.014496', '-0.272', '0.01401', '-0.3176', '-0.288', '-0.1106', '0.4836', '-0.07965', '-0.2483', '-0.0945', '0.9663', '-0.5537', '0.1741', '-0.2465', '0.2239', '0.083', '0.1126', '-0.539', '-0.592', '0.789', '-0.133', '-0.05652', '0.567', '0.2178', '-0.3708', '-0.1604', '-0.555', '0.3364', '0.607', '0.3037', '0.3823', '0.688', '-0.3533', '0.503', '-0.08966', '0.1338', '0.3477', '0.3032', '-0.1276', '0.583', '0.1161', '-0.721', '-1.14', '0.2164', '-0.19', '0.06012', '-0.9727', '-0.4531', '0.4558', '-0.0888', '0.2927', '-0.04547', '-0.2289', '-0.1609', '-0.4204', '-0.0824', '0.5337', '0.1393', '0.4897', '-0.659', '-0.2915', '-0.6885']",C2946,0000333,D002813,170.9,,10008734,0006765
mondo:0008978,chordoma,"['chordoma, susceptibility to', 'notochordal sarcoma', 'notochordoma', 'chordoma', 'susceptibility to chordoma', 'chordoma, malignant', 'chordoma (disease)', 'CHDM']",3302,215400,178,C0008487,"['-0.03436', '0.02013', '0.1298', '-0.34', '-0.3086', '0.3289', '0.6865', '0.4546', '-0.687', '0.02852', '-0.457', '0.1415', '-0.1969', '0.1362', '-0.12494', '0.4844', '-0.4456', '-0.2032', '-0.0612', '-0.604', '-0.2737', '-0.4712', '0.7065', '-0.223', '-0.1908', '-0.05417', '0.1844', '0.0646', '-0.3167', '0.1473', '0.1665', '0.05374', '-0.08124', '-0.43', '-0.2172', '0.12036', '-0.04935', '-0.0737', '0.0711', '-0.1692', '0.03976', '-0.2257', '0.2834', '-0.64', '0.6313', '0.04465', '-0.3047', '-0.1764', '0.02321', '0.1412', '0.1569', '0.2275', '0.002453', '-0.0943', '-0.10876', '0.02957', '0.245', '0.1787', '-0.379', '-0.00492', '0.1671', '0.5205', '-0.2842', '0.1218', '-0.746', '0.4155', '0.4106', '0.358', '0.2656', '0.4263', '0.05264', '0.06174', '-0.1647', '-0.3965', '0.1836', '0.03284', '-0.255', '0.134', '-0.2343', '-0.751', '-0.6963', '0.1197', '0.635', '0.2908', '-0.41', '-0.2235', '0.4153', '0.1622', '0.282', '-0.535', '-0.1694', '-0.2507', '-0.3293', '-0.2075', '0.9917', '-0.2983', '0.3584', '-0.2908', '0.0995', '0.3188']",C2947,,D002817,,,10008747,0010762
mondo:0008979,"chorea, benign familial","['chorea familial benign', 'benign hereditary chorea', 'chorea, benign familial']",,215450,,C1859098,,,,C565851,,,,
mondo:0008980,ataxia-hypogonadism-choroidal dystrophy syndrome,"['BNHS', 'spinocerebellar ataxia, hypogonadotropic hypogonadism, and chorioretinal dystrophy', 'Boucher-Neuhäuser syndrome', 'chorioretinal dystrophy, spinocerebellar ataxia and hypogonadotropic hypogonadism', 'ataxia - hypogonadism - choroidal dystrophy', 'Boucher-Neuhauser syndrome', 'Boucher-Neuhchäuser syndrome']",0111265,215470,1180,C1859093,"['-0.234', '-0.529', '0.0844', '4.5e-06', '-0.11743', '-0.837', '0.2751', '-0.0942', '-0.627', '-0.8833', '0.1204', '-0.1349', '-0.3567', '0.198', '0.584', '-0.4883', '0.129', '-0.1858', '0.1554', '-0.889', '-0.22', '-0.3542', '0.2367', '-0.512', '0.557', '-0.3638', '-0.36', '0.1846', '-0.1497', '-0.8657', '0.02638', '0.3887', '-0.565', '-0.1947', '0.3845', '0.3477', '0.01878', '0.06744', '0.2642', '0.2485', '0.3423', '0.1852', '-0.573', '0.5767', '0.5156', '-0.555', '0.1565', '0.481', '0.286', '0.0375', '0.0544', '0.0663', '0.07166', '-0.5215', '0.0222', '-0.791', '0.3806', '0.295', '-0.3777', '0.364', '-0.3425', '0.2744', '0.2656', '-0.1852', '-0.2898', '0.631', '0.4558', '0.882', '-0.608', '0.339', '0.6665', '0.6147', '0.005917', '-0.5337', '1.007', '0.2152', '0.275', '0.2644', '0.08246', '0.2201', '-0.2903', '-0.614', '0.2137', '0.748', '-0.06137', '-0.669', '0.3643', '-0.06088', '0.5786', '0.4663', '0.4749', '0.374', '0.1309', '-0.02014', '1.037', '0.791', '0.1813', '0.429', '-0.3413', '0.04733']",,,C565850,,,,
mondo:0008981,infantile choroidocerebral calcification syndrome,"['choroid plexus calcification with mental retardation', 'Choroido-cerebral calcification syndrome with retardation', 'choroid plexus calcification and mental retardation', 'choroid plexus calcification with intellectual disability', 'choroid plexus calcification and intellectual disability']",,215480,1313,C1859092,,,,C535357,,,,
mondo:0008982,central areolar choroidal dystrophy,"['choroidal dystrophy', 'areolar atrophy of the macula', 'choroidal dystrophy, central areolar, 1', 'choroidal dystrophy central areolar', 'CACD1', 'CACD', 'central areolar choroidal sclerosis']",,,75377,,"['-0.5776', '-0.02979', '0.004642', '-0.0829', '0.2556', '-0.1207', '-0.0521', '0.1593', '-0.484', '0.04926', '-0.1115', '-0.02708', '-0.324', '-0.1687', '-0.1398', '-0.3418', '0.2466', '-0.1683', '-0.1498', '-0.4705', '-0.3267', '-0.2361', '-0.02489', '0.1769', '-0.02238', '0.008286', '-0.0648', '0.003149', '-0.3022', '0.2144', '0.3442', '-0.08453', '0.0612', '0.02315', '0.0854', '0.3206', '0.09045', '-0.0705', '0.02647', '-0.3333', '0.2913', '-0.4792', '0.12396', '0.0054', '-0.1683', '0.1296', '0.1075', '-0.01337', '0.05777', '0.2412', '0.322', '0.1334', '0.05078', '-0.1307', '-0.0661', '-0.02307', '0.716', '0.1505', '-0.6655', '-0.00776', '0.0924', '-0.05115', '0.10236', '0.11664', '-0.01962', '-0.05807', '0.6216', '0.3394', '-0.2087', '0.0984', '-0.01058', '0.0453', '0.1533', '-0.11774', '0.2264', '-0.10095', '0.0599', '-0.03018', '-0.1584', '-0.2479', '0.207', '-0.1829', '0.1371', '0.483', '-0.1512', '-0.5103', '-0.1063', '0.1359', '0.3247', '-0.1252', '-0.0714', '0.374', '0.2217', '0.1334', '0.4485', '-0.1631', '0.3042', '-0.1636', '-0.1593', '0.2402']",,,C535358,363.54,,,
mondo:0008983,chromosomal instability with tissue-specific radiosensitivity,['chromosomal instability with tissue-specific radiosensitivity'],,215510,,,,,,C565848,,,,
mondo:0008984,ciliary discoordination due to random ciliary orientation,"['ciliary discoordination, due to random ciliary orientation', 'Rutland ciliary disorientation syndrome', 'ciliary discoordination due to random ciliary orientation']",,215518,,C0340038,,,,C562757,759.89,,,
mondo:0008985,ciliary dyskinesia with transposition of ciliary microtubules,"['ciliary dyskinesia with transposition of ciliary microtubules', 'ciliary dyskinesia, due to transposition of ciliary microtubules']",,215520,,C2673817,,,,C567137,,,,
mondo:0008986,circumvallate placenta syndrome,['circumvallate placenta syndrome'],,215550,,C1859089,,,,C565847,,,,
mondo:0008988,citrullinemia type I,"['argininosuccinic acid synthase deficiency', 'CTLN1', 'ASS deficiency', 'CTNL1', 'citrullinemia, classic', 'citrullinemia 1', 'citrullinemia type 1', 'Citrullinuria', 'citrullinemia', 'citrullinemia, type 1', 'argininosuccinate synthetase deficiency', 'classic citrullinemia', 'argininosuccinic acid synthetase deficiency', 'argininosuccinate synthase deficiency']",0070340,215700,247525,,"['-0.5376', '0.5576', '-0.1732', '0.01991', '0.1482', '-0.5522', '-0.4746', '-0.1593', '-0.2705', '0.2252', '-0.735', '-0.5547', '0.235', '0.161', '-0.3347', '-0.3103', '0.1702', '-0.184', '0.04968', '-1.128', '-0.3958', '-0.2231', '0.7275', '-0.3643', '-0.222', '0.1255', '0.0402', '-0.4272', '-0.1669', '-0.4434', '-0.142', '0.7974', '0.4348', '0.2517', '-0.45', '0.1576', '-0.07806', '0.2332', '-0.3042', '-0.2042', '0.44', '-0.4756', '0.2242', '0.3318', '-0.511', '-0.356', '-0.1399', '0.0958', '0.2303', '0.4834', '-0.003645', '-0.3384', '0.01933', '-0.642', '0.06274', '-0.7754', '0.5386', '-0.0996', '-0.5493', '0.3867', '0.1467', '0.1803', '0.5737', '-0.1611', '-0.12134', '0.02676', '0.4211', '-0.06946', '-0.3486', '0.2341', '-0.1177', '-0.11523', '-0.0454', '-0.4373', '0.2211', '0.4082', '-0.06204', '0.1849', '-0.4973', '0.1776', '0.1561', '-0.1658', '-0.3628', '-0.1724', '0.544', '0.4133', '0.2483', '0.273', '0.58', '-0.06494', '0.01029', '0.5547', '0.06445', '0.007282', '0.6797', '0.51', '0.2554', '-0.1812', '0.1849', '0.2434']",C150601,,,,,10058298,
mondo:0008989,citrulline transport defect,['citrulline transport defect'],,215720,,C1859084,,,,C536207,,,,
mondo:0008990,"cleft larynx, posterior","['laryngotracheoesophageal cleft pulmonary hypoplasia', 'cleft larynx, posterior', 'stridor, congenital', 'Novak syndrome']",,215800,93940,,,,,,,,,
mondo:0008991,Verloove Vanhorick-Brubakk syndrome,"['Clh syndrome', 'cleft-limb-heart malformation syndrome', 'cleft-limb-heart malformation syndrome syndrome', 'Verloove Vanhorick Brubakk syndrome', 'cleft limb heart malformation syndrome', 'cleft lip-limb and heart malformations syndrome']",,215850,3429,C1859082,,,,C536541,,,,
mondo:0008992,Juberg-Hayward syndrome,"['cleft lip/palate-abnormal thumbs-microcephaly syndrome', 'cleft LIP/palate with abnormal thumbs and microcephaly', 'Juberg-Hayward syndrome', 'JHS', 'Orocraniodigital syndrome']",,216100,2319,C0796099,,,,C537690,,,,
mondo:0008993,cleft palate-stapes fixation-oligodontia syndrome,"['cleft palate stapes fixation oligodontia', 'cleft palate, deafness, and oligodontia']",,216300,2010,C1859081,,,,C565844,,,,
mondo:0008994,"cleidocranial dysplasia, recessive form","['autosomal recessive form of cleidocranial dysostosis', 'cleidocranial dysplasia, recessive form', 'cleidocranial dysplasia recessive form']",,216330,,C1859080,,,,C565843,,,,
mondo:0008995,Yunis-Varon syndrome,"['cleidocranial dysplasia with micrognathia, absent thumbs, and distal Aphalangia', 'YVS', 'cleidocranial dysplasia-micrognathia-absent thumbs syndrome', 'cleidocranial dysplasia with micrognathia, absent thumbs, and distal aphalangia', 'Yunis Varon syndrome', 'Yunis-Varón syndrome', 'cleidocranial dysplasia, micrognathia, absent thumbs, & distal aphalangia', 'Yunis-Varon syndrome']",0060589,216340,3472,C1857663,"['-0.09106', '0.2203', '0.1448', '-0.346', '0.3328', '-0.3706', '-0.2605', '0.2515', '-0.9243', '-0.5747', '0.001096', '-0.3174', '-0.1395', '0.3306', '0.1151', '0.5312', '-0.0138', '-0.3115', '-0.4502', '-0.5195', '-0.1537', '0.1259', '0.4626', '-0.0657', '0.5215', '-0.05234', '0.04205', '0.05188', '0.3982', '-0.10486', '0.542', '-0.1788', '0.2678', '0.1139', '0.6084', '-0.0396', '0.03345', '0.03577', '0.0426', '-0.263', '-0.10645', '-0.0383', '-0.457', '0.03998', '-0.2031', '-0.232', '0.06683', '0.424', '0.03494', '0.010574', '-0.341', '-0.1356', '-0.2622', '-0.1078', '-0.1713', '-0.2842', '-0.3528', '0.544', '0.2103', '-0.00502', '-0.001635', '0.449', '0.0596', '-0.1897', '-0.4263', '0.42', '0.2246', '0.3716', '-0.4856', '0.208', '-0.4272', '0.117', '-0.1792', '-0.2451', '-0.0523', '0.2556', '0.358', '-0.2524', '-0.04718', '-0.05664', '0.1335', '-0.36', '0.3652', '0.442', '-0.0832', '0.04575', '-0.324', '0.3635', '0.274', '0.2893', '-0.4944', '0.2483', '0.4087', '0.395', '0.44', '0.2428', '0.2847', '-0.1195', '0.501', '0.299']",,,C536719,,,,
mondo:0008998,Cockayne syndrome type 3,"['Cockayne syndrome type 3', 'Cockayne syndrome, type III', 'Cockayne syndrome type C', 'Cockayne syndrome type III']",,216411,90324,,"['-0.2961', '0.3577', '0.1285', '0.01182', '0.228', '-0.3667', '-0.10376', '-0.00913', '-0.356', '-0.31', '0.03036', '0.1882', '0.287', '-0.1821', '-0.1439', '-0.178', '-0.1967', '-0.3125', '-0.000576', '-0.2607', '0.1392', '-0.2083', '0.2527', '0.04868', '0.1954', '0.1503', '-0.08746', '0.132', '0.1166', '-0.0677', '-0.02974', '0.2379', '0.4204', '-0.08514', '0.139', '-0.257', '0.0757', '-0.07855', '-0.04376', '-0.4802', '0.2566', '-0.4272', '0.1725', '0.0908', '-0.1722', '-0.435', '-0.0817', '0.07745', '0.578', '-0.1381', '-0.1433', '-0.3418', '-0.1337', '0.1993', '-0.1445', '-0.2202', '0.5527', '0.04333', '-0.4778', '0.275', '0.273', '0.209', '0.04944', '0.03452', '0.2297', '0.00712', '0.292', '-0.10583', '-0.1527', '0.1882', '-0.4312', '-0.01613', '0.023', '0.0251', '0.1148', '0.1561', '0.0434', '0.1183', '-0.361', '-0.06186', '0.171', '0.11816', '-0.3286', '0.1112', '-0.2537', '-0.0008893', '0.3694', '0.595', '0.2578', '0.1499', '0.11456', '0.0931', '-0.071', '-0.3054', '0.4524', '0.1301', '0.319', '-0.614', '0.01965', '0.0954']",,,,,,,
mondo:0008999,Cohen syndrome,"['Cohen syndrome', 'Coh', 'pepper syndrome', 'Chs1', 'cutis verticis gyrata, retinitis pigmentosa, and sensorineural deafness', 'Chs1, formerly', 'COH1', 'hypotonia, obesity, and prominent incisors']",0111590,216550,193,C1854061,"['0.2974', '0.12225', '-0.01968', '-0.04187', '0.1338', '-0.3933', '0.005665', '1.111', '-0.6987', '-0.752', '0.00979', '-0.005096', '-0.02061', '0.203', '0.2374', '-0.1131', '0.5977', '0.1747', '0.1063', '-0.843', '-0.1004', '-0.2396', '0.01918', '0.0822', '-0.6245', '-0.2094', '-0.3918', '0.3865', '0.0735', '0.1311', '0.597', '-0.3203', '0.5913', '0.565', '-0.0367', '0.254', '-0.0785', '-0.316', '0.0708', '-0.10046', '0.3992', '-0.1037', '-0.5205', '0.2817', '-0.1074', '0.474', '0.4111', '0.1573', '-0.1115', '-0.2391', '-0.434', '0.4226', '-0.283', '-0.0824', '0.10657', '0.03622', '0.0835', '-0.2363', '0.0631', '-0.0506', '0.2086', '0.39', '0.02225', '0.5327', '-0.1735', '-0.1268', '0.1864', '0.4495', '-0.02391', '0.846', '0.04813', '-0.3823', '-0.2151', '0.193', '0.2367', '0.1516', '-0.007397', '-0.3782', '-0.226', '-0.04886', '0.067', '-0.1564', '-0.1296', '0.9453', '-0.1439', '0.3167', '-0.1602', '0.1001', '0.762', '0.4666', '0.4849', '0.3613', '-0.5586', '0.2944', '-0.014404', '-0.00979', '-0.297', '-0.07745', '0.184', '-0.10785']",,,C536438,759.89,,10049066,
mondo:0009000,familial reactive perforating collagenosis,"['collagenosis, familial reactive perforating', 'RPC', 'inherited reactive perforating collagenosis']",,216700,79147,C1857624,,,,C565687,,,,
mondo:0009001,macular coloboma-cleft palate-hallux valgus syndrome,['coloboma of macula and skeletal anomalies'],,216800,91494,C1857619,,,,C565686,,,,
mondo:0009002,"coloboma, ocular, autosomal recessive","['coloboma, ocular, autosomal recessive']",,216820,,C4011974,,,,,,,,
mondo:0009003,achromatopsia 2,"['colorblindness, total', 'achromatopsia caused by mutation in CNGA3', 'achromatopsia 2', 'RMCH2', 'CNGA3 achromatopsia', 'rod monochromatism 2', 'rod monochromacy 2', 'ACHM2', 'Rod monochromatism 2', 'Rod monochromacy 2', 'achromatopsia type 2']",0110007,216900,,C1857618,,C168757,,C536128,,,,
mondo:0009005,complement component C1r/C1s deficiency,"['complement component C1r/C1s deficiency', 'C1r/C1s deficiency']",,216950,,C3150274,,C119991,,,,,,
mondo:0009006,complement component 2 deficiency,"['C2D', 'complement component 2 deficiency', 'complement deficiency caused by mutation in C2', 'C2 deficiency', 'C2 complement deficiency']",0060295,217000,,C3150275,,C119992,,,,,,
mondo:0009007,Jalili syndrome,"['cone-rod dystrophy amelogenesis imperfecta', 'cone rod dystrophy-amelogenesis imperfecta syndrome', 'Jalili syndrome', 'cone-rod dystrophy and amelogenesis imperfecta', 'cone-rod dystrophy with amelogenesis imperfecta']",0111404,217080,1873,CN200616,"['-0.0389', '-0.1855', '-0.1192', '-0.4092', '0.03815', '-0.3213', '-0.1517', '0.4263', '-0.4175', '-0.5063', '-0.0963', '-0.271', '-0.3435', '0.2201', '0.07745', '-0.5586', '0.2483', '-0.2598', '0.00947', '-0.4348', '-0.1558', '-0.1625', '0.0657', '-0.02248', '-0.1765', '-0.006683', '-0.438', '-0.06445', '-0.05124', '0.1257', '0.12213', '0.554', '-0.002935', '-0.10583', '0.09796', '0.0622', '0.05704', '-0.4585', '-0.12054', '-0.3672', '0.2708', '-0.344', '0.1067', '-0.606', '-0.6055', '0.3484', '0.2654', '0.1593', '0.3254', '0.211', '0.776', '0.1908', '0.2411', '-0.6206', '-0.02151', '-0.575', '0.873', '-0.1038', '-0.1538', '-0.1364', '0.268', '-0.4338', '0.11884', '-0.232', '0.2329', '-0.2319', '0.2085', '0.4148', '-0.308', '0.2563', '-0.4229', '-0.005875', '-0.1156', '-0.2966', '0.831', '-0.03093', '0.1254', '0.1871', '-0.2338', '-0.1315', '0.0797', '-0.0762', '0.07214', '0.9863', '-0.2131', '-0.4563', '0.2043', '0.0659', '0.7114', '-0.3125', '0.02467', '0.6455', '0.41', '0.489', '0.431', '-0.1348', '0.1447', '-0.4421', '0.4492', '0.1465']",,,C000596385,520.5,H35.5,,
mondo:0009008,heart defect - tongue hamartoma - polysyndactyly syndrome,"['Ostravik-Lindemann-Solberg syndrome', 'CHDTHP', 'heart defect, tongue hamartoma and polysyndactyly', 'Orstavik Lindemann Solberg syndrome', 'congenital heart defects, hamartomas of tongue, and polysyndactyly']",0111591,217085,1338,C2931046,"['-0.2258', '-0.3552', '0.262', '-0.1107', '0.535', '-0.4268', '0.002563', '0.262', '-0.3416', '-0.4546', '-0.04767', '-0.3064', '0.01456', '-0.2279', '-0.2423', '-0.1635', '-0.10175', '-0.3306', '-0.471', '-0.4517', '0.2947', '0.3093', '0.1735', '-0.07294', '0.304', '0.03528', '-0.1727', '0.2625', '0.635', '-0.1614', '0.2227', '0.01755', '0.1556', '0.06244', '0.335', '-0.436', '0.2406', '0.00512', '0.02676', '-0.47', '0.1384', '0.0435', '0.0757', '0.0335', '0.2167', '-0.3596', '-0.2147', '0.723', '-0.1313', '0.1483', '-0.524', '-0.078', '0.12476', '-0.0827', '-0.5254', '-0.3533', '0.1973', '0.2091', '-0.2734', '-0.03854', '0.1411', '0.394', '0.08923', '-0.1025', '-0.2856', '0.1571', '0.1528', '0.152', '-0.5337', '0.2954', '-0.4092', '-0.1716', '0.1536', '-0.04315', '0.1536', '-0.301', '0.10034', '0.0632', '-0.4368', '-0.2218', '0.03552', '-0.00295', '0.5093', '0.2559', '-0.0346', '-0.1875', '-0.0555', '0.754', '-0.1538', '0.2698', '-0.087', '0.1287', '0.3423', '-0.0507', '0.782', '-0.07983', '0.4954', '-0.583', '0.03888', '0.386']",,,C535849,,,,
mondo:0009009,hypoplasminogenemia,"['ligneous conjunctivitis', 'plasminogen deficiency type 1', 'type 1 plasminogen deficiency', 'plasminogen deficiency, type 1', 'plasminogen deficiency, type I', 'Dysplasminogenemia', 'plasminogen deficiency, type 2']",0111592,217090,97231,C1968804,"['0.004917', '-0.03183', '-0.00933', '-0.2646', '0.06113', '-0.2441', '0.1184', '-0.02277', '-0.2347', '0.0654', '-0.274', '0.09143', '-0.10486', '-0.0935', '-0.2693', '-0.02945', '0.1362', '-0.251', '-0.00295', '-0.3962', '-0.03052', '-0.1763', '0.3318', '-0.06903', '0.01854', '0.1766', '-0.188', '0.131', '0.09595', '-0.1678', '0.03244', '0.0937', '0.1362', '0.1204', '0.1941', '0.02614', '-0.3403', '-0.023', '-0.05222', '-0.0903', '0.03635', '-0.3293', '0.1654', '-0.08813', '0.02127', '-0.01489', '-0.118', '0.1648', '0.0964', '0.1871', '-0.1152', '0.08984', '0.1927', '-0.12195', '-0.2479', '-0.1074', '0.093', '-0.3025', '-0.3582', '-0.08057', '0.1917', '0.4333', '-0.1696', '-0.01534', '0.3723', '-0.11365', '0.3447', '0.1978', '0.09326', '0.258', '-0.1169', '0.0848', '0.10376', '0.005642', '-0.05536', '0.06256', '0.2307', '-0.0684', '-0.0589', '-0.2129', '-0.015495', '-0.2393', '-0.1236', '0.1189', '0.006077', '0.07007', '0.0726', '0.405', '0.0893', '-0.0363', '0.0964', '0.2632', '0.1487', '0.1562', '0.625', '0.04944', '0.2722', '-0.3904', '0.0863', '-0.1332']",,,C580017,,,,
mondo:0009010,aortic arch interruption,,,,2299,,,,,,745.11,Q25.21,10022599,
mondo:0009012,multiple pterygium-malignant hyperthermia syndrome,"['froster-Iskenius-Waterson syndrome', 'contractures, congenital, torticollis, and malignant hyperthermia', 'malignant hyperthermia - arthrogryposis - torticollis', 'froster-Iskenius-Waterson-Hall syndrome', 'malignant hyperthermia arthrogryposis torticollis', 'malignant hyperthermia-arthrogryposis-torticollis syndrome']",,217150,2215,C1857576,,,,C565679,,,,
mondo:0009013,"convulsive disorder, familial, with prenatal or early onset","['convulsive disorder, familial, with prenatal or early onset']",,217200,,C1857575,,,,C565678,,,,
mondo:0009014,cornea plana 2,"['CNA2', 'cornea plana 2, autosomal recessive', 'cornea plana caused by mutation in KERA', 'KERA cornea plana', 'cornea plana 2', 'cornea plana type 2']",,217300,,C1857574,,,,C565677,,,,
mondo:0009015,corneal dystrophy-perceptive deafness syndrome,"['corneal endothelial dystrophy and perceptive deafness', 'corneal dystrophy with progressive deafness', 'CDPD', 'corneal dystrophy and sensorineural deafness', 'congenital corneal dystrophy, progressive sensorineural deafness', 'corneal dystrophy and perceptive deafness', 'Harboyan syndrome', 'Cdpd1']",0111620,217400,1490,C1857572,"['-0.1813', '-0.2145', '-0.535', '0.3384', '0.3643', '-0.8174', '-0.38', '1.025', '-0.06757', '-0.4343', '-0.1964', '-0.4001', '-0.2974', '0.1313', '-0.1349', '-0.2296', '0.4739', '-0.535', '0.05667', '-0.4114', '-0.1699', '-0.457', '0.00899', '0.133', '-0.2318', '-0.3342', '-0.756', '0.03717', '-0.3542', '-0.4', '0.6235', '0.1406', '0.185', '0.554', '-0.1451', '-0.3396', '0.17', '-0.5425', '-0.0217', '0.2593', '0.704', '-0.336', '0.4963', '-0.479', '0.365', '0.2006', '-0.2754', '-0.485', '-0.2408', '-0.154', '0.3542', '-0.376', '-0.2722', '-0.567', '0.4731', '-0.0303', '0.8496', '-0.126', '-0.308', '0.386', '0.2651', '-0.533', '-0.3247', '0.2842', '-0.4644', '-0.3372', '0.3733', '0.919', '-0.2227', '0.52', '0.201', '-0.4478', '0.0914', '-0.2352', '0.7505', '-0.2634', '0.2404', '0.5293', '-0.3882', '-0.1348', '0.2338', '-0.2057', '-0.6587', '0.944', '-0.4553', '-0.2188', '0.5723', '0.3435', '-0.2498', '0.814', '0.4507', '0.4822', '0.3777', '0.272', '0.4841', '-0.4004', '0.3682', '-0.4036', '0.01831', '-0.1514']",,,C535473,,,,
mondo:0009016,band keratopathy,"['band-shaped keratopathy', 'band keratopathy', 'corneal dystrophy, band-SHAPED']",11164,217500,,C0155120,,C118765,,C562399,371.43,,,
mondo:0009017,"corneal degeneration, band-shaped spheroid","['corneal degeneration, band-shaped spheroid']",,217520,,,,,,,,,,
mondo:0009018,central cloudy dystrophy of François,"['central cloudy corneal dystrophy of François', 'central cloudy dystrophy of Francois', 'CCDF', 'corneal dystrophy, central type', 'central cloudy dystrophy of François']",,217600,98972,C1622427,,,,C563262,,,,
mondo:0009019,congenital hereditary endothelial dystrophy of cornea,"['autosomal recessive CHED', 'corneal endothelial dystrophy type 2', 'corneal dystrophy, congenital hereditary endothelial', 'congenital hereditary endothelial dystrophy of the cornea', 'CHED2', 'congenital hereditary endothelial dystrophy type 2', 'corneal endothelial dystrophy 2, autosomal recessive, formerly', 'autosomal recessive congenital hereditary endothelial dystrophy', 'CHED2, formerly', 'corneal endothelial dystrophy 2, autosomal recessive', 'corneal endothelial dystrophy', 'congenital hereditary endothelial dystrophy type II', 'CHEDII', 'corneal endothelial dystrophy 2', 'infantile hereditary endothelial dystrophy', 'CHED', 'corneal endothelial dystrophy, autosomal recessive', 'congenital hereditary endothelial dystrophy of cornea']",0060649,217700,293603,,"['-0.568', '-0.2654', '-0.3784', '0.3606', '0.04843', '-0.3088', '-0.3894', '0.2131', '-0.06238', '0.3418', '0.1854', '-0.1957', '-0.0918', '0.2131', '-0.5244', '-0.2996', '0.3752', '-0.749', '0.3357', '-0.799', '-0.4663', '-0.07434', '0.283', '0.3818', '-0.5166', '0.1061', '-0.8135', '0.12463', '-0.0878', '0.1299', '0.3657', '0.2467', '0.02032', '-0.1548', '-0.1203', '-0.504', '-0.3857', '-0.183', '0.3848', '-0.26', '0.3567', '-0.6387', '-0.3813', '0.0554', '-0.3984', '0.8145', '-0.05557', '-0.05646', '0.1798', '0.5845', '0.6587', '-0.4297', '0.1674', '-0.4102', '0.02412', '-0.09216', '0.4805', '0.1312', '-0.5737', '0.02704', '-0.1486', '-0.4573', '0.01682', '0.345', '0.0412', '-0.06573', '0.695', '0.7236', '-0.3572', '0.6025', '-0.3914', '-0.1102', '0.3586', '-0.2333', '0.43', '0.1758', '-0.05692', '-0.1344', '0.1582', '0.03793', '-0.1313', '-0.04755', '-0.2347', '0.483', '-0.5874', '-0.5347', '0.0553', '0.2603', '0.156', '0.1609', '0.0192', '0.507', '0.382', '0.5015', '0.472', '-0.12134', '0.4243', '-0.6895', '0.2961', '0.1488']",,,C536439,,,,
mondo:0009020,macular corneal dystrophy,"['Mcdc1', 'Groenouw type 2 corneal dystrophy', 'Mcdc1, formerly', 'macular dystrophy, corneal', 'macular corneal dystrophy, type 2', 'corneal dystrophy, macular type', 'Fehr corneal dystrophy', 'macular corneal dystrophy type 1', 'macular dystrophy, corneal type 1', 'macular corneal dystrophy, type 1', 'MCD', 'Groenouw type II corneal dystrophy', 'corneal dystrophy Groenouw type II', 'macular dystrophy, corneal, 1']",2565,217800,98969,C0024439,"['-0.4597', '-0.2014', '-0.3796', '0.431', '0.5137', '-0.6113', '-0.2118', '0.2598', '-0.1521', '-0.811', '0.10315', '-0.493', '-0.2253', '0.514', '-0.2969', '-0.723', '-0.00915', '-0.7153', '0.0632', '-0.7554', '-0.4827', '-0.09247', '0.4814', '0.005756', '-0.3772', '0.1328', '-0.4507', '0.0958', '-0.7446', '0.5747', '0.7363', '0.2542', '-0.16', '-0.0692', '0.2449', '0.1548', '-0.1906', '-0.6636', '0.4038', '-0.07007', '0.4358', '-0.4631', '0.207', '0.3088', '0.04764', '0.907', '-0.0598', '-0.4373', '-0.03738', '0.1116', '0.729', '0.2001', '0.756', '-0.3953', '0.3276', '0.1128', '0.4644', '-0.097', '-0.738', '0.163', '0.2183', '-0.7676', '0.0921', '0.4404', '-0.0867', '-0.2727', '1.151', '0.979', '-0.1893', '0.5786', '-0.2174', '-0.3655', '0.0969', '0.166', '0.604', '0.3796', '-0.1671', '-0.01947', '-0.1655', '-0.129', '-0.0725', '-0.2854', '-0.0412', '0.55', '0.1556', '-0.7935', '-0.52', '-0.08417', '0.02483', '0.1393', '0.49', '0.9204', '-0.07935', '0.371', '0.1101', '-0.01979', '0.4756', '-0.8853', '0.0693', '0.0626']",C34793,,C537834,371.55,H18.55,10025406,
mondo:0009021,Toriello-Carey syndrome,"['corpus callosum agenesis-blepharophimosis-Robin sequence syndrome', 'corpus callosum, agenesis of, with facial anomalies and ROBIN sequence', 'corpus callosum agenesis facial anomalies Robin sequence', 'agenesis of corpus callosum with facial anomalies and Robin sequence', 'Toriello-Carey syndrome']",,217980,3338,C0796184,,,,C563127,,,,
mondo:0009022,"corpus callosum, agenesis of","['corpus callosum agenesis', 'agenesis of corpus callosum', 'isolated corpus callosum agenesis', 'agenesis of the corpus callosum', 'ACC', 'corpus callosum, agenesis of']",,217990,,,,C98905,,D061085,,,,
mondo:0009024,cortical blindness-intellectual disability-polydactyly syndrome,"['cortical blindness, retardation, and postaxial polydactyly']",,218010,1389,C1857568,,,,C565674,,,,
mondo:0009025,apparent mineralocorticoid excess,"['Ame1', 'Ulick syndrome', 'cortisol 11-Beta-ketoreductase deficiency', 'apparent mineralocorticoid EXCESS', '11 Beta-hydroxysteroid dehydrogenase type 2 deficiency', 'apparent mineralocorticoid excess', 'AME', 'APE', '11-beta-hydroxysteroid dehydrogenase deficiency type 2', 'cortisol 11-beta-ketoreductase deficiency', 'apparent mineralocorticoid excess syndrome', 'AME 1', 'syndrome of apparent mineralocorticoid Excess']",4367,218030,320,CN203981,"['-0.1858', '-0.10126', '-0.465', '0.5723', '0.09735', '-0.0949', '-0.2969', '0.876', '-0.874', '-0.1611', '-0.6377', '0.1004', '0.2102', '-0.03952', '-0.3955', '-0.5317', '-0.011696', '0.3428', '0.2059', '-0.545', '0.04086', '-0.278', '0.2087', '-0.3103', '-0.05716', '0.2598', '-0.4255', '0.1315', '0.3857', '0.2391', '0.613', '0.147', '0.4475', '0.1389', '-0.718', '-0.1151', '0.009514', '0.1025', '0.4114', '0.206', '0.294', '-0.746', '0.8926', '-0.914', '0.2341', '0.01842', '0.1294', '-0.0805', '-0.136', '0.1897', '-0.00652', '0.05972', '0.1252', '-0.5566', '-0.4048', '0.941', '-0.03262', '-0.4272', '-0.3125', '0.6353', '0.10297', '0.7554', '-0.1204', '-0.74', '-6.52e-05', '-0.2378', '-0.248', '0.7783', '-0.6177', '0.1577', '0.2534', '-0.1797', '0.709', '0.307', '0.599', '0.1442', '-0.1617', '0.1183', '-0.1272', '0.1305', '-0.1155', '0.3142', '-0.326', '0.541', '-0.00669', '0.2969', '0.2815', '-0.1653', '0.7705', '0.4648', '0.406', '0.2517', '0.1681', '-0.2751', '0.42', '0.4275', '0.5625', '-0.574', '-0.6016', '-0.0808']",C131083,1000817,D043204,255.3,,,
mondo:0009026,Costello syndrome,"['Costello syndrome', 'CSTLO', 'faciocutaneoskeletal syndrome', 'FCS syndrome', 'myopathy, congenital, with excess of muscle spindles', 'congenital myopathy with excess of muscle spindles']",0050469,218040,3071,C0587248,"['0.1472', '0.1105', '0.26', '-0.727', '0.3325', '-0.3938', '0.3574', '0.9976', '-0.63', '-0.2153', '0.1393', '0.4568', '0.05176', '-0.303', '-0.2456', '0.2834', '-0.1444', '-0.5596', '0.04572', '-0.201', '0.00409', '0.02438', '0.3596', '-0.578', '0.3118', '-0.653', '0.3616', '0.6074', '0.2275', '-0.508', '0.74', '-0.04233', '0.7046', '0.06866', '-0.3535', '-0.1355', '0.07825', '-0.0664', '-0.2913', '-0.4663', '-0.4907', '0.0927', '0.4885', '0.3164', '0.05228', '0.368', '-0.1417', '0.2517', '0.558', '-0.2306', '-0.58', '0.603', '-0.087', '-0.0339', '-0.2998', '-0.1304', '0.014336', '0.2137', '-0.11426', '0.2034', '0.3413', '-0.2025', '-0.7334', '-0.05457', '0.271', '0.733', '0.1798', '0.4146', '-0.0709', '1.133', '-0.3806', '-0.315', '-0.467', '-0.0706', '0.000394', '-0.2937', '-0.03882', '-0.2323', '-0.141', '-0.235', '0.02174', '0.1913', '-0.3103', '0.2028', '-0.6113', '0.4373', '0.08923', '0.1364', '0.5107', '-0.3618', '-0.10736', '-0.0816', '-0.34', '-0.04037', '0.1232', '-0.07776', '0.756', '-0.2015', '0.5093', '0.2257']",C84652,,D056685,799.89,,10067380,
mondo:0009027,"cramps, familial adolescent","['cramps, familial adolescent']",,218050,,,,,,,,,,
mondo:0009028,Crane-Heise syndrome,"['Crane-Heise syndrome', 'cleft Lip/palate, agenesis of clavicles and cervical vertebrae, and talipes equinovarus']",,218090,1512,C1857532,,,,C536452,,,,
mondo:0009029,"cranial nerves, congenital paresis of","['cranial nerves, congenital paresis of']",,218100,,C1857531,,,,C565673,,,,
mondo:0009030,"cranial nerves, recurrent paresis of","['cranial nerves, recurrent paresis of']",,218200,,C1857530,,,,C565672,,,,
mondo:0009031,craniodiaphyseal dysplasia,"['CDD', 'craniodiaphyseal dysplasia', 'Lionitis']",0080032,218300,1513,C0410539,"['-0.317', '0.1724', '0.2666', '-0.303', '0.0791', '-0.2625', '0.06384', '0.3389', '-0.2056', '-0.0989', '-0.2178', '0.1334', '0.05392', '-0.001982', '-0.03046', '-0.0993', '0.1599', '-0.06305', '-0.1542', '-0.5244', '0.0429', '0.03976', '0.508', '-0.0901', '0.1995', '0.10754', '-0.0823', '0.00591', '0.0852', '0.1001', '-0.05786', '-0.0358', '0.08606', '0.2128', '0.1276', '-0.2205', '-0.232', '-0.2505', '-0.0971', '-0.3684', '-0.08704', '-0.11005', '0.0468', '-0.42', '-0.010994', '-0.3152', '-0.01665', '0.2493', '0.1104', '-0.0562', '-0.001318', '0.1619', '0.359', '0.01744', '-0.3577', '-0.59', '-0.1274', '0.0741', '-0.05225', '-0.05893', '0.3242', '-0.05743', '-0.341', '0.0546', '-0.10406', '0.04935', '0.3328', '0.2825', '-0.3293', '0.1216', '-0.1116', '0.001034', '0.246', '-0.10706', '-0.1747', '0.1357', '0.06152', '0.1107', '0.03223', '-0.411', '-0.2861', '0.10455', '-0.0642', '0.2798', '-0.11975', '0.1179', '-0.2119', '0.1288', '0.222', '0.04004', '-0.01614', '0.1748', '0.0925', '0.09454', '0.2622', '0.2854', '0.429', '-0.2769', '0.3708', '0.02519']",C131429,,C562940,756.59,,,
mondo:0009032,cranioectodermal dysplasia,"['Sensenbrenner syndrome', 'CED', 'cranioectodermal dysplasia', 'Levin syndrome']",0050577,,1515,CN119432,"['0.3643', '-0.4365', '0.5684', '-0.2544', '0.3958', '-0.2368', '-0.3062', '0.906', '-0.545', '-0.6997', '-0.4119', '-0.532', '-0.3418', '0.04477', '-0.4924', '-0.4526', '0.348', '0.01913', '-0.2522', '-0.845', '0.05353', '-0.0714', '0.2788', '-0.06305', '0.1329', '-0.3362', '-0.4636', '0.1278', '0.333', '-0.7466', '0.1727', '0.1653', '0.02707', '-0.1654', '0.6836', '-0.2542', '-0.4746', '-0.5806', '0.1117', '-0.1926', '-0.0877', '-0.0697', '-0.3164', '0.068', '-0.353', '0.2157', '0.0818', '0.2812', '-0.2717', '-0.316', '-0.3577', '0.638', '0.374', '0.2451', '0.01619', '-0.715', '0.2172', '0.1148', '-0.3635', '0.2174', '0.525', '-0.169', '-0.3086', '-0.2778', '-0.4143', '-0.9053', '0.2842', '0.5356', '-0.3962', '0.02052', '-0.4028', '-0.1793', '0.049', '0.5557', '-0.08124', '-0.4514', '0.4907', '-0.2073', '-0.11304', '-0.0711', '-0.03168', '-0.06647', '0.3572', '0.02695', '-0.508', '0.1686', '-0.0729', '0.2612', '-0.2593', '0.4138', '-0.2688', '0.2031', '-0.006954', '-0.02959', '0.6665', '0.2542', '0.503', '-0.3262', '-0.1175', '0.4307']",C129305,,,756.9,,,
mondo:0009033,temtamy syndrome,"['Temtamy-Shalash syndrome', 'TEMTAMY syndrome', 'craniofacial dysmorphism-coloboma-corpus callosum agenesis syndrome', 'TEMTYS', 'intellectual disability with or without craniofacial Dysmorphism, ocular coloboma, or abnormal corpus callosum', 'craniofacial dysmorphism with ocular coloboma absent corpus callosum and aortic dilatation', 'mental retardation with or without craniofacial Dysmorphism, ocular coloboma, or abnormal corpus callosum', 'temtamy syndrome', 'Dysmorphism, corpus callosum agenesis and colobomas']",0111621,218340,1777,C1857512,"['-0.1349', '0.267', '0.2062', '0.01973', '0.2142', '-0.605', '-0.2329', '0.8174', '-0.4275', '-0.4658', '-0.2091', '-0.504', '-0.08734', '-0.01505', '-0.2197', '0.01246', '-0.03177', '-0.4707', '0.01537', '-0.4863', '0.05945', '0.1252', '0.2347', '-0.2986', '0.1644', '-0.0792', '-0.4653', '-0.11084', '0.3198', '-0.4746', '0.8306', '-0.654', '0.3755', '0.1716', '0.3435', '-0.31', '-0.522', '-0.5244', '-0.2291', '-0.0626', '0.03036', '-0.2012', '0.00852', '0.0966', '0.308', '-0.1826', '-0.10077', '0.09766', '-0.2983', '-0.2306', '-0.0766', '0.4792', '-0.8013', '0.2336', '-0.2319', '-0.3616', '0.2957', '-0.2954', '0.2603', '0.1771', '0.1173', '-0.694', '0.5854', '0.466', '-0.7256', '0.5303', '-0.07745', '0.2407', '-0.1562', '0.361', '-0.2205', '0.2563', '-0.4631', '0.863', '0.1068', '0.08295', '0.2993', '-0.178', '-0.7295', '0.2913', '0.3357', '0.05066', '0.2554', '0.8413', '0.05423', '0.139', '0.2817', '0.3467', '0.4746', '0.601', '0.006245', '0.8154', '-0.2825', '-0.1202', '0.8013', '0.4272', '0.6055', '-0.354', '0.8525', '0.0735']",C148371,,C536959,,,,
mondo:0009034,craniofacial dyssynostosis,"['bilateral lambdoid and sagittal synostosis', 'craniofacial dyssynostosis and short stature', 'craniofacial dyssynostosis with short stature', 'craniosynostosis-craniofacial dysostosis syndrome']",,218350,1516,C1857511,,,,C536455,,,,
mondo:0009035,"craniometaphyseal dysplasia, autosomal recessive","['autosomal recessive craniometaphyseal dysplasia', 'CMDR', 'craniometaphyseal dysplasia, autosomal recessive', 'craniometaphyseal dysplasia, autosomal recessive type']",0080802,218400,,,,,,C536570,,,,
mondo:0009036,"cardiocranial syndrome, Pfeiffer type","['Cardiocranial syndrome', 'craniosynostosis-congenital heart disease-intellectual disability syndrome', 'Pfeiffer Cardiocranial syndrome', 'craniostenosis, sagittal, with congenital heart disease, mental deficiency, and mandibular ankylosis', 'Pfeiffer-type cardiocranial syndrome', 'Pfeiffer Singer Zschiesche syndrome', 'Pfeiffer-Singer-Zschiesche syndrome', 'sagittal craniostenosis with congenital heart disease, mental deficiency and mandibular ankylosis']",,218450,2872,C1857495,,,,C535578,,,,
mondo:0009037,craniosynostosis with anomalies of the cranial base and digits,['craniosynostosis with anomalies of the cranial base and digits'],,218530,,C1857493,,,,C565666,,,,
mondo:0009038,craniosynostosis-fibular aplasia syndrome,"['Lowry syndrome', 'craniosynostosis with fibular aplasia']",,218550,1533,C1857492,,,,C565665,,,,
mondo:0009039,Baller-Gerold syndrome,"['BGS', 'Baller-Gerold syndrome', 'craniosynostosis-radial aplasia syndrome', 'BALLER-Gerold syndrome', 'craniosynostosis with radial defects']",0050654,218600,1225,C0265308,"['0.7295', '-0.01079', '-0.363', '-0.299', '0.131', '-0.2874', '0.5156', '0.6914', '-0.4128', '-0.745', '-0.1622', '0.69', '0.1865', '0.2764', '-0.2566', '0.3267', '0.903', '-0.2717', '-0.517', '-0.7935', '-0.1354', '-0.0583', '0.1221', '-0.4329', '0.729', '0.2164', '-0.255', '0.05707', '0.514', '-0.2355', '0.2225', '-0.0817', '0.05795', '0.1392', '-0.0431', '0.2112', '0.2491', '-0.7905', '-0.3752', '0.08264', '0.0716', '0.183', '0.068', '-0.7783', '-0.05103', '0.0893', '0.00999', '0.532', '0.2021', '-0.256', '-0.2917', '-0.401', '0.1935', '0.274', '-0.644', '-0.05362', '-0.2242', '0.1819', '-0.1968', '0.05695', '0.7964', '0.01149', '-0.0848', '-0.008354', '0.02464', '0.11865', '0.3154', '0.6123', '-0.006332', '0.3135', '-0.1282', '0.446', '0.02246', '-0.3318', '0.4219', '0.1332', '0.414', '-0.5938', '-0.1395', '-0.74', '-0.0656', '0.266', '-0.0383', '0.48', '-0.4875', '-0.4658', '-0.4165', '0.2474', '0.1957', '-0.2272', '0.1204', '0.3694', '0.2329', '0.02927', '0.02206', '-0.0926', '0.9346', '-0.753', '0.1307', '-0.01614']",,,C536788,,,,
mondo:0009040,craniosynostosis-intellectual disability syndrome of 51N and Gettig,"['craniosynostosis-mental retardation syndrome of Lin and Gettig', 'craniosynostosis-intellectual disability syndrome of Lin and Gettig', 'Lin-Gettig syndrome']",,218649,,C1857473,,,,C565664,,,,
mondo:0009041,craniosynostosis-intellectual disability-clefting syndrome,"['Baraitser Rodeck garner syndrome', 'craniosynostosis-intellectual disability-clefting syndrome', 'craniosynostosis, mental retardation, seizures, choroidal coloboma, dysplastic kidneys, bat ears, cleft lip and palate, and beaked nose', 'craniosynostosis mental retardation clefting syndrome', 'craniosynostosis-mental retardation-clefting syndrome', 'craniosynostosis intellectual disability clefting syndrome', 'craniosynostosis, intellectual disability, seizures, choroidal coloboma, dysplastic kidneys, bat ears, cleft lip and palate, and beaked nose']",,218650,,C2931663,,,,C565663,,,,
mondo:0009042,craniotelencephalic dysplasia,"['craniotelencephalic dysplasia', 'Complex of anomalies involving the cranium and brain']",,218670,1528,C1857471,,,,C535597,,,,
mondo:0009043,generalized resistance to thyroid hormone,"['Refetoff syndrome', 'deafness-thyroid hormone resistance syndrome', 'GRTH']",,,3221,,"['-0.1759', '0.4033', '0.1251', '0.01152', '0.2124', '0.00728', '-0.0945', '0.1976', '-0.1092', '-0.519', '-0.11084', '0.03802', '0.1871', '0.01575', '-0.0008984', '-0.305', '-0.2152', '0.0776', '-0.2318', '-0.296', '0.04044', '-0.3438', '0.296', '-0.10675', '0.2275', '0.2898', '0.1482', '-0.2834', '0.27', '-0.2399', '0.2705', '0.2024', '0.03986', '-0.1777', '-0.3667', '-0.07306', '-0.05615', '0.1494', '-0.06274', '-0.378', '-0.00796', '-0.02667', '0.3398', '0.10474', '0.0241', '-0.3813', '0.4243', '-0.009926', '0.603', '-0.03009', '0.10095', '-0.04962', '0.2988', '0.0729', '-0.3386', '0.1597', '0.6934', '-0.2644', '-0.3538', '0.305', '0.317', '0.03473', '0.01242', '-0.1375', '-0.1799', '0.05963', '0.2349', '0.412', '-0.4612', '-0.0564', '-0.1678', '0.01617', '0.10767', '-0.0544', '0.4182', '0.371', '-0.008606', '0.2498', '-0.2028', '-0.00743', '-0.1278', '0.1595', '-0.0979', '-0.2754', '-0.2467', '-0.03008', '0.269', '0.02116', '0.5234', '0.0531', '0.2795', '0.322', '-0.1229', '-0.324', '0.684', '0.0652', '-0.009796', '-0.2979', '-0.4019', '0.3508']",,,,,,,
mondo:0009044,Crigler-Najjar syndrome,"['Crigler Najjar syndrome', 'UGT deficiency', 'hereditary unconjugated hyperbilirubinemia', 'bilirubin-UGT deficiency', 'bilirubin UDP glucuronyl transferase deficiency', 'Crigler-Najjar syndrome', 'bilirubin uridinediphosphate glucuronosyltransferase deficiency']",3803,,205,CN119421,"['0.2432', '0.1808', '-0.3198', '-0.2983', '0.4272', '-0.6387', '-0.3516', '0.8857', '-0.1775', '0.010796', '-0.2056', '-0.405', '0.03397', '0.3103', '-0.4062', '-0.323', '0.03555', '-0.07404', '-0.3145', '-0.9326', '-0.1628', '-0.1256', '0.694', '-0.091', '-0.1666', '-0.06824', '0.108', '-0.3252', '-0.3337', '-0.02779', '0.05945', '0.5005', '-0.167', '0.2106', '-0.793', '-0.1046', '0.4897', '-0.615', '0.0694', '0.2224', '0.2546', '-0.5215', '-0.2532', '0.1671', '-0.1711', '0.3008', '-0.3733', '0.1948', '-0.3062', '-0.1716', '0.1926', '-0.2495', '-0.0551', '-0.4314', '-0.1055', '0.4365', '0.844', '0.1947', '-1.175', '0.4453', '-0.1636', '0.0466', '1.0205', '-0.0891', '-0.02576', '-0.4915', '0.378', '-0.05124', '-0.334', '-0.002573', '0.4163', '0.3105', '0.081', '-0.0601', '0.592', '0.763', '0.661', '-0.1646', '-0.4146', '0.2012', '0.11926', '0.4075', '-0.1858', '0.4507', '0.3628', '0.02736', '0.4678', '0.398', '0.06042', '0.3042', '1.206', '0.429', '0.458', '-0.4915', '0.5254', '0.3228', '-0.01081', '-0.9414', '0.1583', '-0.02338']",C84656,,D003414,,E80.5,10011386,
mondo:0009045,cataract-nephropathy-encephalopathy syndrome,"['crome syndrome', 'congenital cataracts, renal tubular necrosis and encephalopathy in two sisters']",,218900,1380,C0795914,,,,C536216,,,,
mondo:0009046,Fraser syndrome,"['cryptophthalmos with other malformations', 'cryptophthalmos-syndactyly syndrome', 'Meyer-Schwickerath^s syndrome', 'Ulrich-Feichtiger syndrome', 'cryptophthalmos syndrome', 'Fraser syndrome', 'cyclopism', 'cryptophthalmos with Other malformations', 'Fraser-Francois syndrome']",0090001,,2052,C0265233,"['0.2527', '-0.3044', '0.08167', '-0.2847', '0.05283', '0.07556', '0.2896', '0.09784', '-0.5654', '-0.793', '0.1469', '-0.6523', '0.1509', '0.5635', '-0.4883', '0.4084', '-0.1235', '-0.344', '-0.4678', '-0.964', '-0.45', '-0.1399', '0.2482', '-0.08923', '-0.3542', '-0.2727', '-0.3162', '0.422', '1.169', '-0.676', '0.4053', '-0.1788', '0.1354', '0.1564', '-0.0217', '-0.4463', '0.3184', '-0.3704', '-0.34', '0.3564', '-0.467', '0.10767', '0.7124', '-0.3574', '0.01504', '-0.4016', '-0.4858', '0.1989', '-0.2137', '0.663', '-0.7646', '-0.2864', '0.1506', '-0.7495', '-0.2844', '-0.265', '-0.011154', '0.4949', '-0.6343', '-0.1771', '0.3213', '0.1007', '0.1866', '0.699', '0.1765', '0.1176', '0.45', '0.2864', '-0.278', '0.316', '-0.5874', '-0.1832', '-0.1223', '0.602', '-0.3394', '0.0963', '0.0875', '-0.11285', '-0.4583', '-0.1519', '-0.1776', '-0.00561', '0.5938', '0.6807', '-0.2935', '-0.000662', '0.2404', '-0.2141', '-0.3079', '-0.1653', '-0.4568', '0.1483', '-0.077', '0.2979', '0.7485', '0.04886', '0.564', '-0.5767', '0.0798', '0.423']",C118436,,D058497,,,,
mondo:0009047,cryptorchidism,"['cryptorchism', 'undescended testicles', 'undescended testis', 'cryptorchidism', 'cryptorchidism, unilateral or bilateral', 'cryptorchidism (disease)', 'undescended testes', 'undescended testicle']",11383,219050,,,"['-0.05475', '-0.1421', '-0.01545', '-0.005478', '0.2717', '-0.7295', '-0.367', '1.011', '0.164', '-0.8604', '0.283', '0.582', '-0.3804', '1.003', '-0.1141', '-0.098', '-0.1195', '0.3713', '-0.2346', '-0.448', '-0.2927', '0.06274', '0.04727', '-0.4912', '0.4722', '-0.222', '0.558', '0.52', '-0.2124', '-0.152', '0.4507', '-0.3687', '0.2198', '-0.2413', '-0.6416', '0.388', '0.04092', '-0.1814', '0.612', '-0.6216', '-0.10913', '0.887', '-0.2308', '0.1681', '0.2776', '-0.2666', '0.1892', '-0.3', '0.3894', '0.4905', '-0.3862', '-0.5425', '-0.03427', '0.0416', '-0.367', '0.339', '-0.3362', '0.5283', '-0.4365', '0.2163', '-0.00463', '0.2976', '0.2101', '0.3506', '-0.3328', '0.325', '0.511', '0.4292', '-0.2808', '0.9893', '0.06244', '0.2703', '0.516', '-0.4463', '-0.1868', '-0.1436', '0.0823', '0.8086', '-0.358', '-0.5913', '0.07385', '0.6016', '0.3064', '-0.0824', '0.09235', '-0.2183', '0.04837', '0.02478', '0.751', '-0.4492', '-0.8506', '0.5728', '-0.5215', '0.283', '0.347', '0.1909', '-0.1059', '-0.7407', '-0.324', '0.03558']",C12326,0004562,D003456,752.51,,,0000028
mondo:0009048,curved nail of fourth toe,"['curved nail of fourth toe', 'claw-like fingers and toes']",,219070,,,,,,,,,,
mondo:0009049,Cushing syndrome due to macronodular adrenal hyperplasia,"['corticotropin-independent macronodular adrenal hyperplasia', 'primary macronodular adrenal hyperplasia', 'massive macronodular adrenocortical disease', 'MMAD', 'AIMAH', 'ACTH-independent macronodular adrenocortical hyperplasia', 'adrenocorticotropic hormone-independent macronodular adrenal hyperplasia', 'primary bilateral macronodular adrenal hyperplasia', 'ACTH-independent Cushing syndrome']",0111622,,189427,CN200644,,,,C565662,,,,
mondo:0009050,Cushing disease due to pituitary adenoma,"['pituitary adenoma 4, ACTH-secreting, somatic', 'corticotroph adenoma', 'ACTH-secreting pituitary adenoma', 'ACTH producing pituitary adenoma', 'Corticotropinoma', 'pituitary adenoma, ACTH-secreting', 'pituitary-dependent Cushing syndrome', 'Cushing disease', 'corticotroph pituitary adenoma', 'pituitary corticotroph micro-adenoma', 'Cushing^s disease', 'pituitary adenoma 4, ACTH-secreting', 'Cushing disease, pituitary', 'PITA4', 'pituitary dependent Cushing syndrome']",7004,219090,96253,C1306214,,C7462,,D049913,,E24.0,10035109,
mondo:0009051,cutaneous photosensitivity-lethal colitis syndrome,"['early cutaneous photosensitivity and severe colitis', 'cutaneous photosensitivity and colitis, lethal']",,219095,2881,C1857449,,,,C536224,,,,
mondo:0009052,"cutis laxa, autosomal recessive, type 1A","['cutis laxa, autosomal recessive, type IA', 'autosomal recessive cutis laxa type IA', 'cutis laxa, autosomal recessive', 'ARCL1', 'ARCL1A']",0070135,219100,,CN033664,,,,C562628,,,,
mondo:0009053,ALDH18A1-related de Barsy syndrome,"['cutis laxa, corneal clouding, and intellectual disability', 'P5CS deficiency', 'Delta-1-pyrroline 5-carboxylate synthetase deficiency', 'cutis laxa, corneal clouding, and mental retardation', 'ARCL3A', 'neurocutaneous syndrome, Bicknell type', 'autosomal recessive cutis laxa type IIIA', 'progeroid syndrome of De Barsy', 'cutis laxa, autosomal recessive, type 3A', 'De Barsy syndrome a', 'De Barsy syndrome A', 'cutis laxa, autosomal recessive, type IIIA']",0070132,219150,35664,,"['-0.7173', '0.2642', '0.4077', '-0.322', '0.3232', '-0.6675', '-0.1874', '0.5703', '-0.4956', '-0.03998', '-0.2375', '-0.1235', '0.1846', '0.00572', '-0.1417', '0.1401', '0.5024', '-0.02553', '0.1631', '-0.6875', '0.2695', '0.03476', '-0.3623', '-0.2281', '-0.08856', '0.198', '-0.474', '-0.03017', '0.27', '0.0345', '0.1738', '-0.01267', '0.564', '0.5337', '-0.007256', '-0.0985', '-0.06757', '-0.187', '-0.2512', '-0.2766', '0.1503', '-0.3315', '-0.1575', '0.2487', '0.0996', '-0.295', '0.0711', '0.3152', '-0.1655', '-0.0899', '-0.2466', '0.2339', '0.144', '0.1976', '-0.1422', '-0.1443', '0.1248', '-0.1621', '-0.1879', '0.0282', '0.2502', '-0.3386', '-0.4614', '-0.0408', '0.1027', '-0.2703', '0.5127', '0.4707', '-0.11646', '0.3394', '-0.5107', '0.2888', '0.1871', '-0.183', '-0.2244', '-0.1037', '-0.0435', '-0.3125', '-0.1989', '0.1334', '0.1774', '0.3154', '-0.617', '0.614', '-0.1652', '0.0944', '0.2069', '0.6025', '0.457', '0.4475', '0.3762', '0.7217', '0.2255', '0.3162', '0.2351', '0.2488', '0.305', '-0.306', '0.9976', '0.3242']",,,,371.89,,,
mondo:0009054,"autosomal recessive cutis laxa type 2, classic type","['ARCL2A', 'Arcl2', 'autosomal recessive cutis laxa type II classic type', 'ARCL2, Debré type', 'ADCL2', 'autosomal recessive cutis laxa type 2, Debre type', 'ARCL2, classic type', 'autosomal recessive cutis laxa type 2, Debré type', 'ARCL2, Debre type']",0070141,,357074,CN204606,"['0.00839', '0.1832', '0.05865', '-0.1158', '0.1521', '-0.2927', '-0.1061', '0.089', '-0.16', '-0.00915', '-0.153', '-0.0617', '0.03802', '0.005688', '-0.02039', '-0.01496', '0.0662', '-0.04037', '0.0372', '-0.2654', '-0.08014', '-0.1277', '0.1859', '-0.01846', '0.002426', '0.0529', '-0.0907', '-0.09827', '0.1069', '-0.1476', '0.1742', '0.04578', '0.1726', '0.0702', '0.006428', '-0.132', '-0.0647', '-0.11206', '-0.002956', '-0.1597', '0.04483', '-0.249', '0.05234', '0.0413', '-0.0252', '-0.188', '-0.03564', '0.1312', '0.000597', '0.02528', '0.0406', '-0.0681', '0.02441', '-0.0761', '-0.1697', '-0.1309', '0.04572', '-0.03406', '-0.1378', '0.01125', '0.09393', '0.04138', '0.04486', '0.02962', '0.0923', '0.003845', '0.1423', '0.02588', '-0.1733', '0.1968', '-0.2374', '-0.0321', '0.04056', '-0.209', '0.1674', '0.09735', '-0.1257', '-0.05374', '-0.1398', '-0.1754', '0.006386', '-0.01449', '-0.07465', '0.11084', '-0.02873', '0.1128', '0.0721', '0.176', '0.125', '0.02634', '0.1052', '0.1753', '0.11523', '-0.03113', '0.3103', '0.1061', '0.1748', '-0.2172', '0.0834', '0.0764']",,,C562632,,,,
mondo:0009055,cutis marmorata telangiectatica congenita,"['hereditary cutis marmorata telangiectatica congenita', 'cutis marmorata telangiectatica congenita (disease)', 'cutis marmorata telangiectatica congenita', 'CMTC', 'Van Lohuizen syndrome']",,219250,1556,,,,,C536226,757.8,,,0025107
mondo:0009056,cutis verticis gyrata and intellectual disability,"['cutis verticis gyrata and mental retardation', 'cutis verticis gyrata and intellectual disability', 'cutis verticis gyrata-intellectual disability syndrome', 'CVG/MR']",,219300,1557,C1857444,,,,,,,,
mondo:0009057,cyanosis and hepatic disease,['cyanosis and hepatic disease'],,219400,,C1857443,,,,C565660,,,,
mondo:0009058,cystathioninuria,"['cystathionase deficiency', 'cystathioninuria (disease)', 'cystathioninuria', 'Cystathione gamma-lyase deficiency syndrome', 'cystathione gamma-lyase deficiency syndrome', 'gamma-cystathionase deficiency']",0090142,219500,212,C3495552,"['-0.416', '0.3682', '-0.259', '-0.279', '0.1016', '-0.2273', '-0.2512', '0.3284', '-0.015236', '-0.1466', '-0.1355', '0.012375', '0.0688', '-0.3025', '0.06683', '0.04907', '0.2445', '-0.0531', '-0.1584', '-0.891', '-0.1021', '-0.3167', '0.552', '-0.1488', '0.00783', '0.04242', '0.4905', '-0.1547', '-0.05588', '-0.01375', '0.3237', '-0.0878', '-0.0695', '-0.0611', '-0.482', '-0.0723', '0.2218', '-0.498', '0.2708', '-0.3457', '-0.04913', '-0.5557', '0.675', '-0.3083', '-0.274', '-0.3972', '0.1973', '-0.214', '0.02432', '0.34', '0.1364', '-0.001626', '-0.0993', '-0.1715', '-0.00159', '-0.12195', '0.4004', '-0.01965', '-0.517', '0.501', '0.322', '-0.1637', '0.399', '-0.332', '0.1526', '0.06964', '0.08496', '0.014465', '-0.459', '0.2107', '-0.2627', '-0.1676', '-0.289', '0.2668', '0.0297', '0.4153', '0.158', '0.395', '-0.2546', '-0.0495', '0.297', '0.2988', '0.4343', '0.2876', '0.04318', '0.2279', '-0.05658', '0.07776', '0.1912', '0.3865', '0.306', '0.2886', '-0.4565', '-0.2969', '0.7407', '0.4172', '0.2379', '-0.766', '0.0429', '-0.04593']",C129070,,,,,,0003153
mondo:0009059,cysteine Peptiduria,['cysteine Peptiduria'],,219550,,C1857438,,,,C565659,,,,
mondo:0009060,cystic disease of lung,['cystic disease of lung'],,219600,,C1384901,,,,C563237,,,,
mondo:0009061,cystic fibrosis,"['CF', 'cystic fibrosis', 'pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis', 'cystic fibrosis lung disease, modifier of', 'mucoviscidosis']",1485,219700,586,C0010674,"['-0.1688', '0.11383', '-0.1588', '0.2583', '0.1484', '-0.28', '0.526', '0.4458', '-0.3137', '-0.1516', '-0.2532', '-0.424', '-0.4473', '0.735', '-0.02414', '-0.3752', '-0.2617', '0.3125', '-0.3733', '-0.09247', '-0.1967', '-0.602', '0.6387', '-0.1417', '0.1763', '-0.3762', '0.3887', '0.3372', '1.094', '-0.5215', '0.6973', '-0.744', '-0.2096', '-0.1725', '0.3452', '-0.1372', '-0.4856', '-0.0616', '0.5137', '0.293', '-0.391', '0.3767', '-0.1132', '-0.01453', '-0.3381', '-0.1517', '0.03528', '-0.26', '0.4724', '0.641', '-0.4531', '-0.0879', '0.1669', '-0.05453', '0.1667', '-0.1691', '-0.2664', '0.10516', '0.003414', '0.1396', '0.3665', '1.442', '0.531', '0.2083', '-0.10284', '0.1368', '0.4692', '0.4575', '0.0125', '0.248', '0.03482', '0.09283', '0.1935', '-0.4717', '-0.01613', '0.0601', '0.4011', '-0.003248', '0.12164', '0.1304', '0.0866', '-0.0738', '-0.485', '-0.144', '-0.3086', '0.0544', '0.2299', '-0.0683', '0.4138', '-0.1271', '0.1294', '-0.00849', '-0.504', '-0.0539', '0.656', '-0.1748', '-0.262', '-0.821', '-0.428', '0.6133']",C2975,,D003550,277.0,E84,10011762,
mondo:0009062,cystic fibrosis-gastritis-megaloblastic anemia syndrome,"['cystic fibrosis with Helicobacter pylori gastritis, megaloblastic anemia, and intellectual disability', 'cystic fibrosis gastritis megaloblastic anemia', 'cystic fibrosis, Helicobacter pylori gastritis, megaloblastic anemia, subnormal mentality and minor anomalies', 'cystic fibrosis with Helicobacter pylori gastritis, megaloblastic anemia, and mental retardation', 'cystic fibrosis gastritis megaloblastic anaemia', 'Lubani Al Saleh Teebi syndrome', 'Lubani-Al Saleh-Teebi syndrome']",,219721,2575,,,,,C537039,,,,
mondo:0009063,ventriculomegaly-cystic kidney disease,"['congenital nephrosis-cerebral ventriculomegaly syndrome', 'ventriculomegaly with cystic kidney disease', 'VMCKD']",0111625,219730,443988,C1857423,"['-0.003782', '0.01955', '0.004635', '-0.001445', '0.0066', '-0.0331', '0.004818', '0.03001', '-0.0287', '-0.014755', '-0.002888', '-0.006737', '-0.00912', '0.02965', '-0.02815', '-0.02103', '0.005604', '-0.01746', '-0.011406', '-0.05832', '0.00445', '-0.02655', '0.00825', '-0.007362', '0.005726', '-0.02182', '0.004166', '0.006012', '0.00792', '-0.0087', '0.0236', '-0.01391', '0.02783', '-0.003292', '0.01906', '-0.00881', '-0.01741', '-0.007523', '-0.00246', '-0.02345', '0.000382', '-0.01004', '0.01152', '-0.01359', '0.008766', '-0.02618', '-0.001195', '0.01124', '0.01393', '0.01425', '-0.00185', '-0.001559', '0.011086', '-0.004894', '-0.01598', '-0.02705', '0.024', '-0.01619', '-0.03732', '-0.008224', '0.01248', '0.01662', '-0.00837', '0.00505', '0.0005445', '0.00188', '0.0349', '0.03592', '-0.02722', '0.02826', '-0.007004', '0.00904', '0.01794', '-0.0117', '0.005253', '0.02547', '0.01214', '0.00678', '-0.00772', '-0.01213', '-0.01006', '0.002438', '-0.003395', '0.02461', '-0.002157', '-0.01772', '0.004593', '0.004524', '0.03735', '0.01773', '-0.00284', '0.01721', '-0.012085', '0.01575', '0.0497', '0.02388', '0.006783', '-0.01345', '-0.01513', '0.01573']",,,,,,,
mondo:0009064,ocular cystinosis,"['adult-onset cystinosis', 'cystinosis, ocular Nonnephropathic', 'non-nephropathic cystinosis', 'cystinosis, ADULT NONNEPHROPATHIC', 'cystinosis, benign Nonnephropathic']",,219750,411641,C2931013,,,,C535765,,,,
mondo:0009066,juvenile nephropathic cystinosis,"['cystinosis, late-onset juvenile or adolescent nephropathic type', 'juvenile cystinosis', 'intermediate cystinosis', 'cystinosis, intermediate', 'cystinosis, late-onset juvenile or adolescent nephropathic']",,219900,411634,C0268626,"['0.1344', '0.2222', '0.1497', '0.1354', '0.06616', '-0.3052', '-0.4648', '0.0836', '-0.4932', '-0.01677', '-0.5664', '0.1108', '-0.2996', '0.369', '-0.10394', '-0.3838', '-0.01254', '-0.02678', '0.10614', '-0.2756', '-0.004417', '-0.1782', '0.3281', '0.1924', '-0.2301', '-0.1332', '-0.1757', '0.11896', '-0.11584', '-0.224', '0.3777', '0.0991', '0.2659', '0.302', '0.3', '0.1334', '-0.463', '0.1534', '-0.202', '0.03116', '-0.0487', '-0.427', '0.139', '0.06604', '-0.1516', '0.05154', '0.2075', '0.2634', '-0.09784', '0.04678', '-0.0009046', '0.3604', '0.1661', '-0.3286', '0.02605', '-0.515', '0.4233', '0.10614', '-0.3684', '-0.06976', '-0.1666', '-0.2184', '0.1123', '-0.1377', '0.1255', '-0.4253', '0.2551', '0.475', '-0.3848', '-0.2177', '0.00821', '-0.1611', '0.2471', '-0.02728', '0.0421', '0.181', '-0.03552', '0.3494', '-0.0404', '-0.1024', '-0.2429', '-0.3687', '-0.3188', '0.1732', '0.1279', '-0.01156', '0.1547', '-0.1406', '0.3596', '-0.3086', '0.2142', '0.364', '0.01486', '-0.2175', '0.4785', '0.2324', '0.4922', '-0.162', '-0.2002', '0.02817']",,0009049,C562683,,,,
mondo:0009067,cystinuria,"['cystinuria-lysinuria syndrome', 'cystinuria, type A/B', 'cystinuria (disease)', 'cystinuria-lysinuria', 'cystinuria, type non-I', 'cystinuria, type I, formerly', 'cystinuria, type I', 'CSNU', 'cystinuria, type II', 'cystinuria, type III, formerly', 'cystinuria, type a', 'cystinuria, type B', 'cystinuria, type non-I, formerly', 'cystinuria', 'cystinuria, type II, formerly', 'cystinuria, type III']",9266,220100,214,C0010691,"['-0.0847', '0.1511', '-0.02629', '0.0721', '0.06226', '-0.3933', '0.1892', '1.055', '-0.3767', '-0.428', '0.2456', '0.3098', '-0.1403', '0.263', '-0.4617', '-0.1538', '-0.0751', '-0.2096', '0.01814', '-0.767', '-0.6226', '0.03622', '0.4185', '0.2532', '-0.2432', '-0.2593', '-0.08685', '0.1631', '-0.393', '-0.2404', '0.9385', '-0.11', '-0.2318', '0.2292', '-0.8228', '-0.254', '0.2189', '0.2947', '-0.3853', '-0.01558', '-0.4443', '-0.4949', '0.3184', '-0.293', '0.09875', '-0.339', '0.1394', '-0.521', '0.005775', '0.1545', '-0.3188', '0.3096', '-0.0643', '-0.5464', '-0.4736', '-0.1267', '0.675', '0.3115', '-0.517', '0.1396', '0.5444', '0.1903', '-0.0953', '-0.546', '0.3994', '-0.4905', '0.696', '-0.1891', '-0.515', '-0.2954', '0.9287', '-0.3042', '-0.2761', '0.6753', '0.3604', '0.1859', '0.1964', '-0.2886', '-0.328', '-0.1836', '-0.5083', '0.0372', '-0.05203', '0.0888', '0.2069', '0.2888', '-0.0486', '-0.7397', '0.4788', '0.02466', '0.1779', '0.2114', '-0.6646', '-0.5415', '0.6216', '0.3315', '0.2498', '-0.5186', '-0.6416', '0.1798']",C84664,,D003555,,,10011778,0003131
mondo:0009068,cytochrome-c oxidase deficiency disease,"['Complex IV deficiency', 'isolated cytochrome C oxidase deficiency', 'deficiency of mitochondrial respiratory chain complex4', 'isolated COX deficiency', 'mitochondrial complex IV deficiency, nuclear type 1', 'cytochrome C oxidase deficiency', 'isolated mitochondrial respiratory chain complex IV deficiency', 'COX deficiency', 'cytochrome-C oxidase deficiency', 'Complex 4 mitochondrial respiratory chain deficiency', 'mitochondrial Complex 4 deficiency', 'Cox deficiency', 'mitochondrial complex IV deficiency']",3762,220110,254905,C0268237,"['-0.529', '0.226', '0.1514', '0.0676', '-0.0725', '-0.2744', '0.0923', '-0.0846', '-0.4062', '-0.02344', '-0.2299', '-0.314', '-0.1802', '0.2144', '-0.0684', '-0.308', '-0.6367', '-0.3748', '-0.5347', '-0.9536', '0.4583', '-0.3914', '0.7524', '-0.004593', '0.0008926', '-0.2874', '0.136', '-0.02159', '0.158', '0.1554', '0.2106', '0.3682', '0.4126', '0.351', '0.111', '-0.611', '-0.0991', '0.1009', '-0.1406', '0.009155', '-0.2211', '-0.6', '-0.01314', '0.4475', '-0.03433', '-0.4895', '-0.07764', '0.09106', '0.11584', '0.0925', '-0.1434', '0.1218', '0.1444', '-0.1516', '0.0742', '-0.578', '0.477', '0.08405', '-0.265', '0.1666', '-0.2368', '0.1356', '0.8066', '-0.335', '-0.776', '0.0961', '0.3647', '0.4246', '-0.471', '0.3228', '-0.4856', '-0.328', '0.2068', '0.4336', '-0.3308', '0.08966', '0.2537', '0.35', '0.1081', '0.484', '-0.0199', '0.2502', '-0.02335', '0.08746', '0.271', '-0.06177', '0.518', '0.1698', '0.337', '0.1678', '0.3132', '0.379', '0.1707', '-0.1578', '0.3938', '0.4624', '0.6455', '-0.1098', '-0.04108', '-0.3826']",C98910,,D030401,,,,
mondo:0009069,"congenital lactic acidosis, Saguenay-Lac-Saint-Jean type","['Cox deficiency, Saguenay-Lac-Saint-Jean type', 'Leigh syndrome, French-Canadian type', 'COX deficiency, French-Canadian type', 'Leigh syndrome, Saguenay-Lac-Saint-Jean type', 'Cox deficiency, Saguenay Lac saint Jean type', 'cytochrome oxidase deficiency, Saguenay-Lac-Saint-Jean type', 'SLSJ-COX deficiency', 'Leigh syndrome, French Canadian type', 'Leigh syndrome, Saguenay Lac saint Jean type', 'LSFC', 'cytochrome C oxidase deficiency, French Canadian type', 'Cox deficiency, French Canadian type', 'cytochrome C oxidase deficiency, French-Canadian type', 'mitochondrial complex IV deficiency, nuclear type 5, (French-Canadian)']",0111180,220111,70472,,"['-0.09973', '0.3875', '-0.1638', '0.2805', '0.05963', '-0.878', '-0.10645', '0.4602', '-0.2316', '-0.0218', '-0.02588', '-0.3425', '0.7666', '0.099', '0.3972', '0.2903', '0.7095', '0.2917', '-0.3318', '-0.732', '0.1897', '-0.1107', '0.3708', '-0.1153', '-0.0524', '-0.04767', '-0.4294', '-0.06146', '0.3281', '-0.254', '0.4949', '0.258', '0.2102', '-0.05072', '-0.541', '0.172', '-0.3015', '0.5312', '0.3076', '-0.001976', '-0.0685', '-0.5913', '0.2795', '0.254', '0.44', '0.03302', '-0.1018', '-0.0669', '-0.2352', '-0.02919', '-0.7573', '-0.7056', '-0.3452', '-0.4617', '0.5063', '-0.12', '0.5117', '-0.2109', '0.05023', '0.2664', '-0.421', '0.04993', '0.3987', '-0.5273', '-0.0549', '0.536', '0.2235', '-0.1398', '-0.4963', '0.6606', '-0.08246', '0.0793', '0.7983', '0.2861', '-0.3281', '0.715', '0.647', '-0.4243', '-0.6147', '0.2852', '-0.2352', '-0.7954', '-0.5103', '0.5146', '0.2954', '0.5664', '-0.2289', '0.0715', '0.4778', '0.3757', '0.2776', '0.1081', '0.1594', '0.1523', '0.598', '0.2527', '0.387', '-0.2001', '-0.1655', '-0.5254']",,,C537004,,,,
mondo:0009070,D-glyceric aciduria,"['d-glyceric aciduria', 'D-glycericacidemia', 'D-glycerate kinase deficiency', 'non ketotic hyperglycinemia syndrome', 'glycerate kinase deficiency', 'D-glyceric acidemia']",0111626,220120,941,C1291386,"['-0.4746', '0.10504', '0.008194', '-0.2764', '-0.1646', '-0.537', '-0.4238', '0.638', '-0.313', '-0.03552', '-0.2435', '-0.2793', '0.11053', '-0.01845', '-0.04016', '0.02994', '0.2097', '-0.0383', '-0.3938', '-0.8003', '0.1854', '-0.2253', '0.3267', '-0.252', '0.3525', '-0.5586', '0.065', '-0.000484', '-0.09674', '-0.1876', '0.483', '-0.09485', '0.3223', '0.1608', '-0.4907', '-0.345', '-0.2467', '-0.2852', '-0.1663', '-0.06476', '0.1407', '-0.5454', '0.2058', '0.00907', '-0.3936', '-0.5186', '0.2448', '-0.4143', '-0.1002', '0.3574', '-0.1186', '0.1293', '-0.4192', '0.1299', '0.3826', '-0.3472', '0.321', '-0.12463', '-0.265', '0.5215', '0.1672', '-0.11237', '0.303', '-0.0808', '0.01555', '-0.05814', '0.2157', '0.3682', '-0.4502', '0.03342', '-0.2817', '0.09326', '-0.3396', '0.3633', '0.0648', '0.3533', '0.5146', '-0.1722', '-0.1215', '0.3894', '0.4343', '0.3865', '0.1581', '0.2932', '0.2773', '0.3728', '-0.02097', '0.236', '0.4463', '0.3186', '0.251', '0.5728', '-0.265', '-0.2485', '0.5947', '0.868', '0.09094', '-0.1774', '0.3425', '-0.1871']",C128804,,C535767,,,,
mondo:0009071,hereditary renal hypouricemia,"['Dalmatian hypouricemia', 'renal hypouricemia', 'hypouricemia, renal']",,,94088,,"['0.2847', '-0.5117', '-0.7363', '0.2325', '0.1508', '-0.4043', '-0.1896', '0.525', '0.1274', '-0.2695', '-0.1617', '0.12396', '-0.0938', '0.692', '-0.2112', '0.2905', '-0.2793', '0.05856', '0.1624', '-0.5005', '-0.09814', '-0.5693', '0.78', '0.2742', '0.1292', '-0.1221', '0.4148', '-0.2825', '0.11273', '-0.355', '0.2052', '-0.4102', '0.2612', '0.2798', '-0.4153', '-0.656', '0.1725', '-0.02869', '-0.071', '-0.4644', '-0.5386', '-0.4753', '0.8813', '-0.3699', '0.12146', '-0.3955', '-0.3054', '-0.1641', '0.2012', '0.689', '0.0416', '-0.1931', '0.01305', '-0.7583', '-0.2083', '0.1478', '0.6914', '0.1029', '-1.194', '0.0403', '0.5425', '-0.1407', '-0.1472', '-0.282', '-0.04068', '0.08496', '0.4329', '0.643', '0.05295', '0.2737', '-0.1406', '-0.3037', '-0.2773', '0.2052', '0.3096', '0.4773', '0.1987', '0.1985', '-0.1373', '-0.072', '0.1262', '0.3638', '0.10834', '0.4658', '-0.00712', '0.2693', '0.1698', '-0.8584', '0.0719', '-0.37', '0.611', '-0.03412', '-0.5767', '-0.04718', '0.496', '0.3423', '0.773', '-0.02274', '-0.9277', '-0.4268']",,,C537757,790.6,,,
mondo:0009072,Dandy-Walker syndrome,"['atresia of foramina of Magendie and Luschka', 'Dandy-Walker syndrome', 'mega cisterna magna (type of DW complex)', 'Dandy-Walker complex', 'Dandy-Walker malformation', 'Dandy-Walker variant (type of DW complex)', 'Dandy-Walker syndrome or malformation (type of DW complex)', 'isolated Dandy-Walker malformation', 'DW complex', 'DWS', 'Dandy-Walker syndrome, Isolated cases']",2785,220200,217,C0010964,,C75012,1000890,D003616,,,10048411,
mondo:0009073,Ritscher-Schinzel syndrome 1,"['Ritscher-Schinzel syndrome type 1', 'Dandy-Walker-like malformation with atrioventricular septal defect', '3C syndrome', 'RTSC1', 'Ritscher-Schinzel syndrome', 'WASHC5 Ritscher-Schinzel syndrome', 'Ritscher-Schinzel syndrome 1', 'Ritscher-Schinzel syndrome caused by mutation in WASHC5', 'RTSC', 'Craniocerebellocardiac dysplasia']",0060571,220210,,,,,,,,,,
mondo:0009074,facial dysmorphism-macrocephaly-myopia-Dandy-Walker malformation syndrome,"['Dandy-Walker malformation with mental retardation, macrocephaly, myopia, and BRACHYTELEPHALANGY', 'Dandy-Walker malformation with intellectual disability, macrocephaly, myopia, and BRACHYTELEPHALANGY']",,220219,1970,C1857352,,,,C535985,,,,
mondo:0009075,Dandy-Walker malformation-postaxial polydactyly syndrome,"['Dandy-Walker malformation with postaxial polydactyly', 'Pierquin syndrome', 'DWM with postaxial polydactyly']",,220220,1566,C1857351,,,,C535771,,,,
mondo:0009076,autosomal recessive nonsyndromic hearing loss 1A,"['DFNB1A', 'deafness, digenic, GJB2/GJB3', 'deafness, digenic, GJB2/GJB3, Autosomal recessive, Digenic dominant', 'DFNB1', 'deafness, autosomal recessive 1A', 'deafness, autosomal recessive type 1A', 'autosomal recessive deafness 1A', 'autosomal recessive nonsyndromic deafness 1A', 'connexin 26 deafness', 'deafness nonsyndromic, connexin 26 linked', 'deafness, digenic, GJB2/GJB6', 'autosomal recessive nonsyndromic deafness type 1A', 'deafness, autosomal recessive 1a, autosomal recessive, digenic dominant', 'GJB2-related deafness', 'deafness, digenic GJB2/GJB6, Autosomal recessive, Digenic dominant']",0110475,220290,,,,C129022,,C567134,,,,
mondo:0009077,"deafness, congenital, and familial myoclonic epilepsy","['deafness, congenital, and familial myoclonic epilepsy']",,220300,,C1857348,,,,C565649,,,,
mondo:0009079,DOORS syndrome,"['Eronen syndrome', 'deafness onychodystrophy osteodystrophy and mental retardation syndrome', 'brachydactyly due to absence of distal phalanges', 'deafness-onychodystrophy-osteodystrophy-intellectual disability-seizures syndrome', 'DOORS syndrome', 'Digitorenocerebral syndrome', 'deafness-onychodystrophy-osteodystrophy-intellectual disability syndrome', 'door syndrome', 'drc syndrome', 'deafness, onychodystrophy, osteodystrophy, intellectual disability, and seizures syndrome', 'deafness-onychoosteodystrophy-intellectual disability syndrome', 'DOORS', 'autosomal recessive deafness-onychodystrophy syndrome', 'deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures syndrome', 'deafness onychodystrophy osteodystrophy and intellectual disability syndrome']",0111627,220500,79500,,"['0.418', '0.316', '0.0728', '0.0903', '0.1799', '-0.1644', '-0.2908', '0.877', '-0.4548', '-0.7754', '-0.1444', '-0.6006', '0.05908', '0.304', '-0.3052', '0.3142', '0.2156', '-0.4019', '-0.01506', '-0.5356', '0.3364', '-0.08844', '-0.04385', '0.09235', '0.1649', '-0.3845', '-0.77', '0.2744', '0.4941', '-0.0419', '0.6562', '0.007267', '-0.2021', '0.09357', '-0.2861', '-0.5864', '-0.2009', '-0.7295', '-0.3838', '0.1355', '0.2573', '-0.3955', '0.2825', '0.07855', '-0.01736', '-0.588', '0.1381', '0.12054', '0.1162', '0.511', '-0.06335', '0.1097', '-0.39', '-0.07446', '-0.3306', '-0.2366', '-0.0357', '0.04578', '-0.099', '0.194', '-0.1504', '-0.0737', '-0.01101', '0.0686', '-0.518', '0.1757', '0.2534', '0.817', '-0.3618', '0.1288', '-0.1565', '0.234', '-0.3333', '0.1743', '0.03119', '0.2015', '0.7295', '-0.4185', '0.1477', '0.496', '0.0821', '0.57', '0.1543', '0.2686', '-0.3318', '0.09247', '-0.4153', '-0.0002198', '0.1163', '0.9243', '0.0551', '0.5776', '0.1609', '0.211', '0.05875', '0.1354', '0.231', '-0.4136', '0.7324', '0.5347']",,,C563052,,,,
mondo:0009080,split hand-foot malformation 1 with sensorineural hearing loss,"['SHFM1D', 'deafness, congenital, with split hands and feet', 'split-hand/foot malformation 1 with sensorineural hearing loss, autosomal recessive', 'split-hand/foot malformation 1 with sensorineural hearing loss', 'congenital deafness with split hands and feet', 'split hand-split foot-deafness syndrome']",0090024,220600,71271,C1857344,"['0.891', '-0.2222', '0.4663', '0.6753', '-0.445', '-0.04617', '0.8965', '0.9844', '-0.1065', '-1.125', '0.3052', '0.03745', '-0.2642', '0.3562', '-0.4592', '-0.581', '-0.547', '-0.0562', '-0.5444', '-0.2883', '0.12476', '0.4568', '-0.6685', '0.3586', '0.843', '0.443', '-1.105', '0.05008', '-0.4116', '-0.152', '-0.1417', '-0.0847', '0.2944', '-0.04532', '-0.4082', '-0.3079', '-0.37', '-0.4863', '-0.1819', '-0.8774', '0.1681', '-0.04883', '-0.3215', '-0.662', '0.2517', '-0.373', '-0.0303', '0.578', '0.3394', '-0.3992', '-0.00902', '-0.487', '-0.3528', '-0.149', '0.252', '0.578', '-0.12305', '-0.2041', '-0.3098', '0.5845', '-0.1022', '0.8364', '-0.3567', '0.0841', '-0.625', '0.3176', '-0.6343', '0.825', '-0.4841', '-0.2505', '0.02017', '0.675', '1.041', '-0.8076', '0.606', '-0.02495', '0.7773', '0.3237', '0.1981', '-0.1399', '0.1211', '-0.7563', '-0.2512', '0.835', '0.4111', '-0.317', '-0.0002097', '1.518', '0.05707', '0.8506', '0.3018', '0.3494', '-0.2291', '0.666', '0.7246', '0.0732', '0.1587', '-1.279', '-0.06', '-0.09753']",,,C565647,,,,
mondo:0009081,"deafness, congenital, with total albinism","['deafness, congenital, with total albinism']",,220900,,C1857343,,,,C565646,,,,
mondo:0009082,high myopia-sensorineural deafness syndrome,"['deafness and myopia', 'DFNMYP', 'deafness and myopia syndrome']",0111628,221200,363396,CN204687,"['0.09454', '0.257', '0.0565', '0.1559', '0.08875', '-0.12317', '0.4253', '0.1726', '0.1407', '-0.11176', '-0.3247', '-0.01839', '-0.3164', '0.2117', '-0.2917', '-0.402', '0.1796', '-0.1232', '0.08044', '-0.06082', '0.0588', '-0.2242', '-0.05182', '0.1449', '0.3125', '0.2307', '-0.39', '0.1638', '-0.0618', '0.0823', '0.237', '0.0774', '0.3503', '0.399', '0.1691', '-0.4832', '-0.2188', '-0.1707', '-0.2189', '-0.4177', '-0.1007', '-0.0275', '0.001294', '-0.1702', '0.0764', '0.06052', '0.1646', '-0.1443', '0.2123', '-0.1473', '0.1902', '-0.12463', '0.1261', '0.05728', '-0.3696', '-0.05112', '0.08405', '0.001327', '-0.1395', '-0.1179', '0.06244', '-0.07544', '-0.284', '0.06854', '-0.3325', '-0.04184', '0.11896', '0.649', '-0.2435', '0.561', '-0.143', '0.4739', '0.1102', '-0.2961', '-0.04163', '-0.04953', '0.2695', '0.4229', '-0.09045', '-0.0796', '0.05368', '-0.5005', '0.078', '0.658', '-0.1449', '-0.1478', '0.1288', '0.3481', '0.0756', '0.4116', '0.218', '0.7', '-0.0968', '0.1768', '0.5283', '-0.187', '0.382', '-0.2264', '-0.06647', '0.4011']",,,,,,,
mondo:0009083,conductive deafness-malformed external ear syndrome,"['conductive deafness with malformed external ear', 'conductive hearing loss-malformed external ear syndrome', 'deafness, conductive, with malformed external EAR', 'Mengel-Konigsmark syndrome', 'Ear deformity and conductive hearing loss', 'familial congenital moderate neural hearing loss', 'conductive hearing loss and malformed low-set ears', 'conductive deafness - malformed external ear']",,221300,3216,C1857341,,,,C565644,,,,
mondo:0009084,conductive deafness-ptosis-skeletal anomalies syndrome,"['deafness conductive ptosis skeletal anomalies', 'deafness, conductive, with ptosis and skeletal anomalies', 'Jackson Barr syndrome', 'Jackson-Barr syndrome']",,221320,3236,C1857340,,,,C535993,,,,
mondo:0009085,deafness-vitiligo-achalasia syndrome,"['congenital deafness with vitiligo and achalasia', 'deafness, congenital, with vitiligo and achalasia', 'deafness vitiligo achalasia']",,221350,3239,C1857339,,,,C565642,,,,
mondo:0009086,deafness-small bowel diverticulosis-neuropathy syndrome,"['deafness, nerve type, with mesenteric diverticula of small bowel and progressive sensory neuropathy', 'nerve type deafness with mesenteric diverticula of small bowel and progressive sensory neuropathy', 'Groll Hirschowitz syndrome', 'Groll-Hirschowitz syndrome']",,221400,3217,C1857338,,,,C537305,,,,
mondo:0009087,"deafness, neural, congenital moderate","['deafness, neural, congenital moderate']",,221500,,C1857337,,,,C565640,,,,
mondo:0009088,"deafness, neural, with atypical atopic dermatitis","['deafness, neural, with atypical atopic dermatitis']",,221700,,C1857334,,,,C565639,,,,
mondo:0009089,deafness-oligodontia syndrome,"['congenital profound sensorineural deafness and oligodontia', 'deafness oligodontia syndrome', 'deafness-oligodontia syndrome', 'autosomal recessive sensorineural hearing impairment, dizziness, and hypodontia']",,221740,3230,C1857333,,,,C538049,,,,
mondo:0009090,"hearing loss, sensorineural, autosomal-mitochondrial type","['deafness, sensorineural, autosomal-mitochondrial type']",0111752,221745,,,,,,C565637,,,,
mondo:0009091,non-acquired combined pituitary hormone deficiency with spine abnormalities,"['deafness, sensorineural, with pituitary dwarfism', 'Pituitary hormone deficiency, combined with rigid cervical spine', 'CPHD3', 'Deafness, sensorineural with pituitary dwarfism', 'Winkelmann-Bethge-Pfeiffer syndrome', 'pituitary hormone deficiency, combined, type 3', 'non-acquired combined pituitary hormone deficiency-sensorineural hearing loss-spine abnormalities syndrome', 'non-acquired combined pituitary hormone deficiency-deafness-rigid cervical spine syndrome', 'pituitary hormone deficiency, combined, 3', 'pituitary hormone deficiency, combined, with rigid cervical spine']",,221750,231720,C3489787,"['-0.709', '0.0917', '0.5645', '-0.4907', '0.39', '0.1392', '0.3445', '0.3733', '-0.484', '-0.3672', '-0.1267', '-0.0392', '0.00605', '-0.05008', '-0.1289', '-0.2385', '0.1105', '-0.216', '-0.7764', '-0.4827', '-0.1119', '-0.1396', '0.2383', '-0.04892', '0.1552', '0.08484', '-0.04575', '-0.3462', '0.1724', '-0.1771', '0.2251', '0.1375', '0.2627', '0.04733', '-0.1171', '-0.2512', '-0.0361', '-0.4011', '-0.1516', '-0.2142', '0.10187', '0.1317', '0.2551', '-0.00654', '0.0687', '-0.2505', '0.0536', '-0.0873', '-0.02693', '0.3079', '-0.11975', '0.2202', '0.326', '0.1438', '-0.4988', '0.1788', '0.0003495', '-0.1576', '0.0984', '0.3596', '0.1676', '0.01525', '-0.2993', '-0.02893', '-0.3225', '0.0912', '0.2213', '0.5176', '-0.2202', '0.0327', '-0.2998', '0.184', '0.2656', '-0.3037', '0.00809', '-0.04523', '0.03348', '-0.1798', '-0.0721', '0.003447', '-0.1467', '0.1589', '0.1316', '0.3674', '0.0167', '-0.00457', '0.005077', '0.11884', '0.712', '0.2607', '0.1691', '0.388', '0.234', '-0.03055', '0.675', '-0.075', '0.3735', '-0.3076', '0.3447', '0.4534']",,,C536710,,,,
mondo:0009092,polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly,"['dementia, progressive, with lipomembranous polycystic osteodysplasia', 'dementia, prefrontal, with bone cysts', 'polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy', 'PLO-SL', 'polycystic lipomembranous osteodysplasia with sclerosing leukoencephaly', 'brain-bone-fat disease', 'NHD', 'PLOSL', 'progressive dementia with lipomembranous polycystic osteodysplasia; brain-bone-fat disease', 'presenile dementia with bone cysts', 'Nasu-Hakola disease']",0090112,,2770,C1857316,"['0.02791', '0.2266', '0.1842', '-0.1476', '-0.2499', '-0.666', '0.0824', '0.9297', '-0.2563', '0.3804', '-0.954', '0.2106', '-0.1681', '0.1306', '0.623', '-0.2236', '-0.1805', '0.02623', '-0.3022', '0.00657', '-0.1283', '-0.3767', '0.2322', '-0.136', '-0.0745', '-0.6304', '0.03041', '0.11273', '-0.4353', '0.2379', '0.2349', '-0.3037', '-0.3042', '0.1231', '0.63', '-0.1349', '-0.3894', '-0.6294', '-0.581', '0.1508', '0.2607', '-0.1144', '0.5356', '-0.4329', '0.5327', '0.1364', '-0.6577', '-0.04974', '-0.3384', '0.588', '0.07275', '0.2546', '0.0206', '-0.1365', '0.03616', '-0.4172', '0.1758', '-0.6216', '-0.4443', '-0.1307', '0.2163', '-0.04437', '-0.2175', '0.08136', '-0.4321', '-0.0637', '0.476', '0.497', '-0.0945', '0.3518', '-0.04166', '-0.4172', '0.01411', '-0.1277', '0.08795', '0.23', '-0.09235', '0.06903', '0.07587', '-0.01242', '1.55e-05', '-0.429', '0.2135', '0.52', '0.3098', '0.2412', '0.2057', '-0.01403', '0.4573', '0.0764', '0.33', '0.3567', '-0.3103', '0.3354', '0.05396', '-0.1135', '0.1418', '-0.474', '-0.04733', '-0.1769']",,,,758.89,,,
mondo:0009093,dermatoleukodystrophy,['Dermatoleukodystrophy'],,221790,1659,C1857314,,,,C538220,,,,
mondo:0009094,dermochondrocorneal dystrophy,"['dermochondrocorneal dystrophy', 'FranC^ois syndrome', 'Francois syndrome', 'Dermochondrocorneal dystrophy of François', 'DCCD', 'François syndrome']",,221800,79149,C0432288,,,,C535375,379.99,,,
mondo:0009095,"dermatoosteolysis, Kirghizian type","['autosomal recessive syndrome of skin ulceration, arthroosteolysis with pseudoacromegaly, keratitis, and oligodontia', 'Dermatoosteolysis Kirghizian type', 'Kirghizian Dermatoosteolysis', 'dermatoosteolysis, Kirghizian type']",,221810,1657,C1857301,,,,C535373,,,,
mondo:0009097,"persistent hyperplastic primary vitreous, autosomal recessive","['autosomal recessive persistent hyperplastic primary vitreous', 'PHPVAR', 'persistent foetal vasculature', 'persistent fetal vasculature', 'persistent hyperplastic primary vitreous, autosomal recessive', 'retinal nonattachment and falciform detachment', 'retinal nonattachment, nonsyndromic congenital']",,221900,300337,C1969783,"['-0.3582', '0.0813', '0.1553', '-0.0545', '0.2103', '-0.005856', '-0.02043', '0.02826', '-0.3066', '-0.0396', '-0.1656', '-0.1078', '-0.1026', '-0.02237', '-0.2279', '-0.138', '0.02101', '-0.0795', '0.2106', '-0.4736', '-0.1001', '-0.0465', '0.01935', '-0.1556', '-0.014915', '0.1398', '-0.1602', '0.0259', '0.1002', '0.2311', '0.127', '0.01776', '0.259', '0.1456', '0.012665', '0.1788', '0.02141', '-0.16', '-0.1443', '-0.3564', '0.2109', '-0.0711', '0.2041', '-0.09406', '-0.2235', '-0.00527', '0.003304', '-0.04504', '0.1707', '0.10547', '0.1764', '-0.07367', '0.1866', '-0.2073', '-0.2345', '-0.275', '0.3926', '-0.07904', '-0.4348', '-0.09644', '0.265', '-0.04645', '0.04306', '-0.0641', '0.10266', '-0.1713', '0.441', '0.3416', '-0.2153', '0.2544', '-0.2803', '0.09546', '0.1217', '-0.2351', '-0.03357', '-0.1109', '-0.0834', '0.0917', '-0.1786', '-0.1824', '-0.03445', '0.1104', '0.0783', '0.3806', '-0.136', '-0.2018', '0.1105', '0.1676', '0.1153', '0.12305', '0.1351', '0.4673', '0.1189', '0.1567', '0.521', '-0.08234', '0.4153', '-0.3699', '0.0689', '0.2178']",,,,,,,
mondo:0009098,dextrocardia with unusual facies and microphthalmia,"['dextrocardia with unusual facies and microphthalmia', 'dextrocardia, microphthalmia, cleft palate, choreoathetosis and intellectual disability', 'dextrocardia, microphthalmia, cleft palate, choreoathetosis and mental retardation', 'Aughton syndrome']",,221950,,C1857298,,,,C538269,,,,
mondo:0009099,nephrogenic diabetes insipidus-intracranial calcification syndrome,"['diabetes insipidus nephrogenic mental retardation and intracerebral calcification', 'diabetes insipidus, nephrogenic, with intellectual disability and intracerebral calcification', 'diabetes insipidus, nephrogenic, with mental retardation and intracerebral calcification', 'Schofer Beetz Bohl syndrome', 'Schofer-Beetz-Bohl syndrome', 'diabetes insipidus nephrogenic intellectual disability and intracerebral calcification']",,221995,3145,,,,,,,,,
mondo:0009100,type 1 diabetes mellitus 1,"['juvenile-onset diabetes', 'diabetes, type 1, susceptibility to', 'diabetes mellitus, insulin-dependent-1', 'diabetes mellitus, insulin-dependent', 'insulin-dependent diabetes mellitus 1', 'type 1 diabetes mellitus', 'IDDM1', 'diabetes mellitus, type 1', 'diabetes mellitus, insulin-dependent, 1', 'IDDM']",,,,,,,,,,,,
mondo:0009101,Wolfram syndrome 1,"['Wfs', 'WFS1 Wolfram syndrome', 'Wolfram syndrome type 1', 'Wolfram syndrome caused by mutation in WFS1', 'diabetes insipidus and mellitus with optic atrophy and deafness', 'WFS1', 'WOLFRAM syndrome 1', 'Wolfram syndrome 1']",0110629,222300,,,,,,,,,,
mondo:0009102,diaminopentanuria,"['Diaminopentanuria', 'cystine-lysinuria']",,222350,,C1857285,,,,C565630,,,,
mondo:0009103,diaphragmatic hernia 2,"['hernia, congenital diaphragmatic 2', 'diaphragmatic hernia 2', 'DIH2']",,222400,,,,,,C565629,,,,
mondo:0009104,Donnai-Barrow syndrome,"['diaphragmatic hernia-exomphalos-hypertelorism syndrome', 'diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and proteinuria', 'syndrome of ocular and facial anomalies, telecanthus and deafness', 'Holmes-Schepens syndrome', 'DBS/FOAR syndrome', 'diaphragmatic hernia-hypertelorism-myopia-deafness syndrome', 'faciooculoacousticorenal syndrome', 'FOAR syndrome', 'facio-oculo-acoustico-renal syndrome', 'diaphragmatic hernia, exomphalos, absent corpus callosum, hypertelorism, myopia, sensorineural deafness, and Proteinuria', 'Donnai-Barrow syndrome', 'diaphragmatic hernia exomphalos absent corpus callosum hypertelorism myopia sensorineural deafness and proteinuria']",0090144,222448,2143,C1857277,"['0.449', '0.1306', '0.2118', '-0.303', '0.02817', '0.002005', '0.3782', '1.166', '-0.5474', '-0.0934', '0.3801', '-0.2043', '0.05582', '0.2627', '-0.3438', '0.03372', '0.1149', '0.1106', '0.288', '-0.2695', '0.2335', '0.097', '0.3938', '0.4392', '0.2407', '-0.2316', '-0.9585', '-0.05774', '0.6465', '0.595', '0.409', '-0.823', '0.8105', '-0.3833', '-0.287', '-0.3528', '-0.2251', '-0.1318', '0.2717', '-0.1458', '-0.0899', '0.11035', '0.3484', '-0.58', '0.5933', '-0.1835', '-0.09247', '-0.2477', '-0.392', '-0.1719', '-0.0977', '0.10034', '-0.225', '-0.704', '-0.4304', '-0.1929', '0.2803', '-0.5938', '-0.4233', '0.1572', '0.00596', '-0.271', '0.00973', '0.3618', '-0.2333', '-0.1779', '0.2444', '0.602', '-0.4968', '0.296', '0.03117', '0.3547', '-0.04498', '-0.3108', '0.2827', '0.03195', '0.5815', '-0.3477', '-0.461', '-0.05075', '0.3118', '0.5967', '0.2173', '1.081', '-0.314', '0.32', '0.05017', '0.273', '0.1118', '0.4543', '0.4497', '0.6206', '-0.06775', '0.2559', '0.9624', '-0.609', '0.374', '-0.2827', '0.9175', '0.5967']",,,C536390,759.89,,,
mondo:0009105,trichohepatoenteric syndrome,"['Trichohepatoenteric syndrome type 1', 'syndromic diarrhea/Tricho-hepato-enteric syndrome', 'THES1', 'phenotypic diarrhoea', 'syndromic diarrhea', 'Syndromatic diarrhoea', 'SD/THE', 'Trichohepatoenteric syndrome', 'Syndromatic diarrhea', 'Tricho-hepato-enteric syndrome', 'phenotypic diarrhea', 'syndromic diarrhoea']",0111414,,84064,C1857276,"['0.07477', '0.4253', '0.1442', '-0.325', '0.3674', '-0.4045', '0.04065', '0.597', '-0.433', '-0.471', '0.295', '0.02118', '0.0792', '-0.08466', '-0.4219', '-0.07056', '0.6562', '0.3088', '-0.1805', '-0.633', '0.01619', '-0.645', '0.67', '-0.64', '0.2343', '-0.1589', '-0.8247', '-0.2169', '-0.02446', '-0.915', '0.747', '-0.1735', '0.0881', '0.2328', '0.02435', '0.2395', '-0.1122', '0.2026', '-0.3325', '0.536', '-0.2554', '0.5034', '-0.0022', '-0.2773', '-0.2026', '0.2229', '-0.2515', '-0.1808', '-0.3926', '0.03424', '-0.3936', '0.2241', '0.1685', '0.3164', '-0.2583', '0.687', '0.12054', '-0.663', '-0.001062', '0.4993', '0.8994', '0.461', '-0.4673', '-0.0684', '0.0828', '-0.3157', '0.3503', '0.5166', '-0.2214', '0.6646', '0.3486', '0.198', '0.396', '0.4194', '0.01097', '-6.33e-05', '0.5693', '-0.2607', '-0.4065', '0.2754', '-0.1516', '0.00933', '-0.3364', '0.0791', '0.0774', '0.2229', '-0.121', '0.505', '0.621', '0.318', '0.815', '0.1365', '0.01089', '0.309', '0.4385', '0.555', '-0.3958', '-0.803', '0.784', '0.08875']",,,,,,,
mondo:0009106,diastematomyelia,"['Dimyelia', 'diastematomyelia', 'diplomyelia', 'SCM type 1', 'split cord malformation type 1', 'split cord malformation', 'split spinal cord malformation', 'SSCM', 'Pseudodiplomyelia']",,222500,1671,C0011999,,C98913,,,742.51,Q06.2,10012750,
mondo:0009107,diastrophic dysplasia,"['DTD', 'diastrophic dysplasia', 'DD', 'diastrophic dwarfism', 'diastrophic dysplasia, Broad bone-Platyspondylic variant']",14687,222600,628,,"['-0.434', '0.471', '-0.02351', '-0.2634', '0.7075', '-0.8955', '-0.01884', '1.037', '-0.7476', '-0.5884', '0.1156', '0.704', '0.3098', '0.2155', '0.2051', '-0.00402', '0.2366', '0.09503', '-0.2705', '-0.514', '-0.473', '0.07227', '0.631', '-0.1929', '0.05328', '0.4395', '-0.10645', '0.4114', '0.4954', '-0.205', '0.1022', '-0.3718', '-0.07465', '0.3545', '-0.3103', '-0.127', '-0.0834', '-0.3457', '-0.1052', '0.08264', '-0.0783', '-0.0726', '0.288', '0.4832', '0.5576', '-0.3594', '-0.2964', '0.2976', '0.494', '0.2063', '-0.4016', '-0.10297', '0.3887', '-0.3696', '0.1332', '-0.9272', '0.1788', '-0.1522', '-0.3667', '0.2834', '0.10504', '0.1959', '-0.3809', '0.4692', '-0.1425', '0.08453', '0.3533', '0.1991', '-0.04068', '-0.3962', '0.01892', '-0.3657', '0.3333', '-0.09064', '0.1146', '-0.101', '0.10065', '0.1355', '-0.067', '-0.796', '-0.02731', '-0.10645', '0.211', '0.6084', '-0.3608', '0.4358', '-0.2822', '0.1787', '-0.0662', '0.2607', '-0.333', '0.503', '-0.414', '-0.1182', '0.1814', '0.01026', '0.905', '-0.422', '0.6353', '0.241']",C156311,,C536170,756.89,Q77.5,,
mondo:0009108,hyperdibasic aminoaciduria type 1,"['dibasic amino aciduria I', 'dibasic amino aciduria type 1', 'dibasic aminoaciduria 1', 'dibasic amino aciduria 1']",,222690,1032,C2673736,,,,C567132,,,,
mondo:0009109,lysinuric protein intolerance,"['LPI', 'hyperdibasic aminoaciduria', 'Dibasicamino aciduria II', 'lysinuric protein intolerance', 'lysinuric PROTEIN intolerance', 'dibasic aminoaciduria 2', 'dibasic amino aciduria II', 'hyperdibasic aminoaciduria type 2', 'dibasic amino aciduria 2']",0060439,222700,470,C0268647,"['-0.4785', '0.4387', '-0.1409', '-0.1625', '0.09546', '-0.6143', '-0.1671', '0.1558', '-0.003723', '0.325', '-0.1083', '0.2179', '0.10846', '-0.2085', '-0.3906', '-0.3513', '-0.239', '0.1029', '-1.005', '-0.633', '0.12286', '-0.822', '0.2197', '-0.772', '0.001299', '-0.5566', '-0.3215', '0.4482', '0.1666', '-0.1111', '0.5513', '0.0808', '0.2776', '-0.327', '0.1605', '-0.3423', '-0.1912', '0.14', '0.337', '0.0982', '-0.3682', '-0.4446', '0.4004', '-0.01492', '-0.437', '-0.01657', '0.4836', '-0.3665', '0.6694', '0.318', '-0.4019', '0.0554', '0.3457', '-0.3218', '0.0905', '-0.415', '0.633', '-0.1964', '-0.3928', '0.0267', '0.5063', '0.306', '0.06143', '-0.4016', '0.293', '-0.4932', '0.609', '-0.1411', '-0.78', '-0.2498', '-0.3914', '-0.11707', '-0.1527', '0.4194', '-0.1846', '0.2546', '0.3894', '-0.603', '0.1882', '-0.0199', '0.11743', '-0.4426', '-0.02238', '0.1971', '-0.3784', '0.4138', '-0.002907', '0.0737', '0.1137', '-0.0758', '-0.05322', '0.2129', '-0.3179', '-0.417', '0.384', '0.832', '0.289', '-0.559', '-0.125', '0.00798']",C121563,,C562687,270.8,,10058300,
mondo:0009110,dicarboxylic aminoaciduria,"['glutamate-aspartate Transport defect', 'Dicarboxylicaminoaciduria', 'DCBXA', 'glutamate-aspartate transport defect', 'dicarboxylic aminoaciduria']",0060650,222730,2195,C1857253,"['-0.1132', '-0.02792', '0.06046', '-0.2869', '-0.1708', '-0.2284', '-0.1791', '0.4568', '-0.1292', '-0.4978', '-0.2927', '-0.4475', '-0.2181', '-0.05664', '-0.1254', '-0.02132', '-0.0618', '0.1726', '-0.4165', '-0.4116', '0.303', '-0.2239', '0.11945', '-0.34', '0.1482', '-0.2827', '-0.3345', '-0.2108', '0.04773', '-0.3008', '0.004562', '-0.2786', '0.11444', '0.3196', '0.01747', '-0.1931', '-0.05048', '0.04105', '-0.02498', '0.1525', '0.1665', '-0.3235', '-0.1975', '-0.2078', '-0.1292', '-0.3977', '0.26', '-0.1547', '-0.31', '-0.02942', '-0.3118', '-0.1433', '-0.0971', '-0.1368', '-0.1593', '0.09973', '0.4856', '-0.1473', '-0.3933', '0.3777', '0.2893', '-0.03625', '0.254', '-0.281', '-0.08203', '-0.1886', '0.1917', '0.336', '-0.6978', '0.2346', '0.02814', '0.2334', '-0.236', '0.1016', '0.0525', '0.492', '0.2244', '0.02275', '-0.1779', '0.252', '0.504', '0.1504', '0.2961', '0.00978', '0.04865', '0.194', '0.1527', '0.3484', '-0.01758', '0.0596', '0.249', '-0.01248', '-0.1992', '-0.1874', '0.5713', '0.344', '0.2913', '-0.4507', '-0.03494', '-0.00674']",,,C536171,,,,
mondo:0009111,dihydropyrimidinuria,"['DPYSD', 'Dph deficiency', 'dihydropyrimidinuria', 'Dpys deficiency', 'dihydropyrimidinase deficiency']",0111629,222748,38874,,"['-0.2964', '0.141', '0.1197', '-0.251', '-0.007088', '-0.2257', '-0.0768', '0.2446', '-0.1283', '-0.09143', '-0.2399', '-0.1406', '-0.2366', '-0.0992', '-0.1876', '-0.04358', '0.0914', '-0.0173', '-0.3997', '-0.5137', '0.1577', '-0.2041', '0.1053', '-0.3074', '0.0465', '-0.0701', '-0.00771', '-0.1267', '0.1809', '-0.4365', '0.1533', '-0.01121', '0.432', '0.2837', '-0.03674', '-0.02269', '-0.05124', '-0.197', '-0.2191', '0.09064', '0.1033', '-0.2542', '0.00843', '-0.0754', '-0.1565', '-0.4226', '0.243', '-0.02206', '-0.2744', '0.285', '-0.405', '0.1879', '-0.1138', '-0.1964', '-0.081', '0.1654', '-0.04617', '0.0516', '-0.1691', '0.293', '0.2216', '0.1383', '0.1719', '-0.18', '0.1848', '-0.013855', '0.2299', '0.3657', '-0.2457', '0.3125', '-0.02557', '0.1716', '-0.1075', '-0.07324', '-0.03757', '0.02667', '0.2556', '-0.453', '0.127', '0.10455', '0.05536', '0.1199', '-0.11633', '0.2267', '0.2208', '0.201', '0.1252', '0.03458', '0.423', '0.1445', '0.4', '0.2126', '-0.0846', '-0.0633', '0.4573', '0.5576', '0.3477', '0.0428', '0.3206', '-0.01465']",,,,277.2,,,
mondo:0009112,rhizomelic chondrodysplasia punctata type 2,"['peroxisomal dihydroxyacetonephosphate acyltransferase deficiency', 'rhizomelic chondrodysplasia punctata, type 2', 'chondrodysplasia punctata, rhizomelic, due to Dihydroxyacetonephosphate acyltransferase deficiency', 'rhizomelic chondrodysplasia punctata caused by mutation in GNPAT', 'Dihydroxyacetonephosphate acyltransferase deficiency', 'type 2 rhizomelic chondrodysplasia punctata', 'RCDP2', 'Gnpat deficiency', 'Glyceronephosphate O-acyltransferase deficiency', 'GNPAT rhizomelic chondrodysplasia punctata', 'Dhapat deficiency', 'chondrodysplasia punctata, rhizomelic, due to dihydroxyacetonephosphate', 'rhizomelic chondrodysplasia punctata type 2', 'Rcdp2']",0110852,222765,309796,C1857242,"['-0.418', '0.3572', '0.1857', '-0.2834', '0.2654', '-0.4246', '-0.1123', '0.0703', '-0.5903', '-0.1011', '-0.1394', '0.2795', '0.1077', '-0.1087', '0.1624', '-0.05066', '0.1324', '0.00276', '-0.1898', '-0.4473', '0.0398', '0.1127', '0.4077', '-0.2257', '-0.065', '0.2551', '0.04666', '-0.10394', '0.1334', '-0.01519', '-0.08923', '-0.01785', '0.154', '0.11786', '0.1209', '0.1301', '0.0337', '-0.1976', '-0.05356', '-0.2253', '0.132', '-0.4536', '-0.09436', '0.1376', '-0.2457', '-0.149', '-0.02342', '0.1987', '0.2737', '-0.0617', '-0.00514', '-0.1844', '0.1356', '-0.04242', '-0.209', '-0.54', '0.2908', '0.09894', '-0.0755', '0.09265', '0.2395', '-0.0835', '0.02544', '0.04565', '0.07434', '0.05286', '0.299', '0.1313', '-0.4104', '0.0869', '-0.2756', '-0.08527', '0.07996', '-0.27', '-0.12177', '0.008125', '-0.00645', '0.18', '-0.2407', '-0.1797', '-0.02635', '0.01232', '-0.146', '0.183', '-0.1181', '-0.216', '0.07355', '0.4988', '0.1539', '0.08777', '-0.03552', '0.1992', '0.1782', '0.09607', '0.3406', '0.03595', '0.43', '-0.4272', '0.2766', '-0.01956']",,,C537607,,,,
mondo:0009113,hemolytic anemia due to diphosphoglycerate mutase deficiency,"['bisphosphoglycerate mutase deficiency', 'DPGM deficiency', 'diphosphoglycerate phosphatase deficiency', 'diphosphoglycerate mutase deficiency of erythrocyte', 'BPGM deficiency', 'bisphosphoglyceromutase deficiency', 'erythrocytosis, familial, 8']",0111630,222800,714,C1291620,"['-0.398', '0.2947', '-0.0656', '0.2905', '0.63', '-0.0625', '-0.3308', '0.4634', '-0.291', '-0.4592', '0.8027', '0.0003386', '0.2175', '0.45', '-1.234', '-0.07324', '-0.575', '0.1946', '-0.3752', '-0.5723', '-0.07935', '-0.5586', '0.2465', '-0.35', '0.7144', '-0.5903', '-0.0957', '-0.3718', '0.735', '-0.00928', '0.091', '0.2257', '0.3423', '0.779', '0.4246', '-0.2258', '-0.8784', '-0.4993', '0.4404', '-0.3767', '-0.805', '0.273', '0.04224', '-0.379', '-0.848', '-0.98', '0.281', '0.1051', '0.6274', '-0.1793', '0.409', '0.2578', '0.704', '-0.05316', '0.4846', '-0.8237', '0.12286', '0.4038', '-0.954', '0.1927', '-0.1259', '0.4028', '-0.0643', '-0.3018', '-0.0417', '0.3923', '0.3933', '0.805', '-0.4915', '0.9043', '0.782', '-0.2783', '-0.536', '-0.6475', '0.4502', '1.217', '0.2407', '0.3933', '0.11597', '0.3826', '0.2117', '-0.03096', '-0.07837', '0.0719', '0.6187', '-0.582', '-0.522', '0.3735', '0.8286', '-0.09705', '0.5', '0.3303', '-0.1519', '-0.1263', '0.586', '1.075', '0.1643', '-0.2717', '0.03912', '-0.437']",C131638,,,,,,
mondo:0009114,congenital sucrase-isomaltase deficiency,"['sucrose-isomaltase malabsorption, congenital', 'sucrose isomaltose enzyme deficiency', 'SI deficiency', 'congenital sucrose-isomaltase malabsorption', 'genetic sucrase-isomaltose malabsorption', 'CSID', 'sucrase-isomaltase deficiency, congenital', 'sucrose intolerance, congenital', 'sucrose-isomaltose malabsorption, congenital', 'disaccharide intolerance', 'congenital sucrose intolerance', 'sucrose intolerance congenital', 'disaccharide intolerance, 1', 'congenital sucrase-isomaltose malabsorption', 'disaccharide intolerance 1']",0111633,222900,35122,C1283620,"['-0.432', '0.0514', '-0.2593', '0.5703', '0.1853', '-0.3252', '-0.7793', '0.655', '-0.214', '-0.0696', '-0.1794', '0.1882', '0.3203', '0.4187', '-0.387', '0.4355', '-0.221', '-0.2145', '-0.3967', '-0.688', '-0.2822', '-0.607', '0.794', '0.01467', '0.1847', '-0.358', '-0.3403', '0.4407', '0.39', '-0.3943', '0.5635', '-0.1382', '0.1542', '0.4646', '-0.3628', '-0.1736', '-0.4934', '0.0941', '0.1129', '0.1616', '-0.366', '-0.4963', '-0.2202', '0.1962', '0.2428', '-0.296', '0.015236', '-0.485', '0.3774', '0.68', '-0.01042', '-0.2805', '-0.007446', '-0.3037', '-0.2283', '0.2427', '0.2712', '-0.3164', '-0.486', '0.1028', '0.055', '0.5913', '0.65', '-0.573', '0.511', '0.545', '0.8354', '-0.11865', '0.5947', '-0.3623', '-0.2404', '-0.1742', '-0.3198', '0.0929', '0.4739', '0.4407', '0.677', '-0.4026', '-0.4912', '-0.3691', '0.168', '-0.1564', '0.2742', '-0.002546', '0.02611', '0.627', '0.2888', '-0.326', '0.868', '-0.4268', '0.2137', '0.2976', '-0.0546', '-0.1757', '0.1782', '0.3586', '-0.3901', '-0.6084', '0.0691', '0.11316']",C128190,,C538139,271.3,,10066387,
mondo:0009115,congenital lactase deficiency,"['lactase deficiency, congenital', 'Alactasia, congenital', 'disaccharide intolerance 2']",0111646,223000,53690,,"['-0.2406', '0.07544', '0.03555', '0.0916', '0.1495', '-0.1859', '-0.2644', '0.17', '-0.0976', '-0.0922', '-0.09735', '0.006992', '-0.03033', '0.08813', '-0.1846', '0.0432', '-9.62e-05', '0.02342', '-0.2917', '-0.469', '-0.1447', '-0.3188', '0.2266', '-0.075', '0.00598', '-0.1233', '-0.1761', '0.04315', '0.1256', '-0.375', '0.04968', '-0.02869', '0.2029', '0.1951', '-0.121', '0.1156', '-0.1349', '0.01634', '-0.0689', '0.04388', '-0.1311', '-0.2386', '0.1293', '-0.1776', '-0.1578', '-0.07806', '0.00182', '0.1547', '0.04236', '0.2603', '-0.2546', '-0.1398', '0.01563', '0.001329', '-0.1963', '-0.002481', '0.1864', '-0.0801', '-0.2507', '0.08167', '0.2856', '0.1405', '0.1447', '-0.1451', '0.2423', '-0.0152', '0.3396', '0.148', '-0.2678', '0.1855', '-0.1494', '0.0353', '-0.0658', '-0.11017', '-0.0419', '0.03583', '0.1963', '-0.1909', '-0.09174', '0.04343', '-0.1105', '-0.1119', '-0.0596', '0.09644', '0.0663', '0.1586', '0.1342', '0.06125', '0.4104', '-0.1675', '0.04065', '0.1471', '0.05188', '0.0166', '0.37', '0.1422', '0.184', '-0.4353', '0.02457', '0.0787']",,,C562600,271.3,E73.0,,
mondo:0009118,disseminated sclerosis with narcolepsy,['disseminated sclerosis with narcolepsy'],,223300,,C1857229,,,,C565621,,,,
mondo:0009119,"diverticulosis, small-intestinal","['diverticulosis, small-intestinal']",,223320,,C1857228,,,,C565620,,,,
mondo:0009120,"diverticulosis of bowel, hernia, and retinal detachment","['marfanoid syndrome, De Silva type', 'diverticulosis of bowel, hernia, and retinal detachment', 'Marphanoid syndrome type De Silva']",,223330,2464,C1857227,,,,C565619,,,,
mondo:0009121,von Voss-Cherstvoy syndrome,"['phocomelia thrombocytopenia encephalocele and urogenital malformations', 'phocomelia, thrombocytopenia, encephalocele, urogenital malformations', 'DK phocomelia syndrome', 'von Voss-Cherstvoy syndrome', 'phocomelia-thrombocytopenia-encephalocele-urogenital malformations syndrome', 'Von Voss Cherstvoy syndrome']",,223340,3439,C1857226,,,,C565618,,,,
mondo:0009122,Dohle bodies and leukemia,['Dohle bodies and leukemia'],,223350,,C1857225,,,,C565617,,,,
mondo:0009123,orthostatic hypotension 1,"['norepinephrine deficiency', 'dopamine BETA-HYDROXYLASE deficiency, congenital', 'orthostatic hypotension 1, due to DBH deficiency', 'congenital dopamine beta-hydroxylase deficiency', 'dopamine beta hydroxylase deficiency', 'noradrenaline deficiency']",0090145,223360,230,C0342687,"['-0.4082', '0.04745', '-0.457', '0.4277', '-0.4324', '-0.309', '0.1696', '0.868', '-0.4768', '0.01567', '-0.1023', '0.255', '0.179', '-0.04837', '0.0916', '0.06305', '0.1829', '0.73', '-0.3865', '-0.6655', '0.2883', '0.00307', '0.4392', '0.1774', '-0.3213', '-0.05945', '-0.5854', '0.07715', '-0.8184', '-0.3635', '0.607', '0.1732', '0.352', '0.4832', '-0.5806', '-0.2141', '0.281', '-0.557', '-0.03705', '0.2683', '0.329', '-0.1222', '0.3757', '0.0746', '0.1337', '0.1208', '0.1057', '0.275', '0.05225', '0.5386', '-0.2583', '0.4412', '0.05893', '0.10406', '-0.1069', '0.2805', '0.2544', '-0.2627', '-0.3677', '0.07947', '0.3374', '0.785', '0.4026', '-0.3425', '0.06976', '-0.3367', '0.503', '0.558', '-0.4211', '0.1305', '-0.269', '0.06494', '0.1676', '0.1768', '-0.06125', '0.4917', '0.1338', '0.4033', '-0.3538', '0.608', '-0.1433', '-0.3445', '0.1733', '0.5884', '0.544', '0.549', '0.02112', '-0.1715', '0.793', '-0.3735', '0.319', '0.0761', '0.001135', '-0.05533', '0.1531', '0.2798', '0.5615', '-0.0843', '-0.3987', '0.535']",,,C535600,270.8,,,
mondo:0009124,Dubowitz syndrome,"['Dubowitz syndrome', 'intrauterine growth retardation, short stature, microcephaly, mild mental retardation with behaviour problems, eczema, and unusual and distinctive faci', 'intrauterine growth retardation, short stature, microcephaly, mild intellectual disability with behaviour problems, eczema, and unusual and distinctive faci', 'Dubowitz^s syndrome', 'dwarfism-eczema-peculiar facies syndrome', 'intrauterine growth retardation, short stature, microcephaly, mild intellectual disability with behavior problems, eczema, and unusual and distinctive faci', 'intrauterine growth retardation, short stature, microcephaly, mild mental retardation with behavior problems, eczema, and unusual and distinctive faci']",14796,223370,235,C0175691,,C125591,,C535718,742.8,,10059589,
mondo:0009126,duodenal atresia,"['duodenal atresia', 'duodenal atresia (disease)', 'duodenal stenosis', 'atresia of duodenum', 'congenital duodenal atresia', 'congenital atresia of duodenum']",0080216,223400,1203,C0266174,,C101025,,C535720,751.1,,10013812,0002247
mondo:0009127,"dwarfism, low-birth-weight type, with unresponsiveness to growth hormone","['dwarfism, low-birth-weight type with unresponsiveness to growth hormone', 'dwarfism, low-birth-weight type, with unresponsiveness to growth hormone']",,223500,,C1857197,,,,C565615,,,,
mondo:0009128,"dwarfism, intellectual disability, and eye abnormality","['dwarfism, intellectual disability, and eye abnormality', 'Mollica syndrome', 'dwarfism, mental retardation, and eye abnormality']",,223540,2650,C0796076,,,,C535809,,,,
mondo:0009129,"dwarfism, proportionate, with hip dislocation","['dwarfism, proportionate, with hip dislocation', 'dwarfism, proportionate with hip dislocation']",,223550,,C1857196,,,,C565614,,,,
mondo:0009130,Dyggve-Melchior-Clausen disease,"['Dyggve-Melchior-Clausen disease', 'DMC syndrome', 'Dyggve-Melchior-Clausen syndrome', 'DMC', 'DMC disease', 'pseudo-Morquio disease type I']",0111167,223800,239,C0265286,"['-0.2013', '-0.02948', '0.3293', '-0.3755', '0.3745', '-0.522', '-0.04205', '1.087', '-0.8105', '-0.9155', '-0.4368', '0.522', '0.152', '0.186', '0.1992', '0.2605', '0.3801', '0.242', '-0.3171', '-0.718', '-0.4648', '0.4634', '0.7197', '0.1263', '-0.1079', '-0.2236', '0.02322', '0.05167', '0.0483', '-0.0686', '0.522', '-0.1467', '-0.1619', '0.4434', '-0.0944', '0.04532', '-0.1698', '-0.714', '0.4185', '-0.0436', '0.0862', '-0.01424', '0.1396', '0.1732', '0.1393', '-0.3528', '-0.4084', '0.193', '0.2727', '-0.4253', '0.1807', '-0.02861', '-0.2695', '0.176', '-0.1987', '-1.017', '-0.2041', '0.1603', '-0.01357', '0.10724', '0.1708', '0.083', '-0.9717', '0.12476', '-0.541', '-0.06793', '0.823', '0.249', '-0.084', '-0.03616', '-0.259', '-0.708', '0.3284', '-0.02351', '-0.1744', '0.2261', '-0.441', '-0.328', '-0.904', '-0.2382', '-0.264', '0.342', '-0.587', '0.4993', '0.05786', '0.2107', '0.112', '0.00913', '0.4465', '0.329', '0.1053', '0.1466', '-0.5977', '0.4583', '0.187', '-0.10974', '0.83', '-0.3499', '0.1558', '0.3555']",C124844,,,,,,
mondo:0009131,Riley-Day syndrome,"['familial autonomic nervous dysfunction', 'neuropathy, hereditary sensory and autonomic, type 3', 'hereditary sensory and autonomic neuropathy type III', 'hereditary sensory and autonomic neuropathy 3', 'hereditary sensory and autonomic neuropathy type 3', 'neuropathy, hereditary sensory and autonomic, type III', 'dysautonomia, familial', 'HSAN III', 'Riley-Day syndrome', 'HSAN 3', 'familial dysautonomia', 'hereditary sensory neuropathy type 3', 'HSN 3', 'HSAN3', 'Riley Day syndrome']",11589,223900,1764,C0013364,"['0.01526', '0.3135', '-0.13', '0.04343', '0.0691', '-0.5386', '-0.2852', '1.075', '-0.02483', '0.3928', '0.505', '-0.03934', '-0.1989', '0.4019', '0.2322', '0.653', '0.316', '-0.0556', '-0.3196', '-0.559', '0.0856', '-0.651', '0.1364', '0.1511', '0.02136', '-0.0965', '0.1934', '0.1357', '-0.1405', '0.04846', '0.5205', '0.1528', '-0.0892', '0.1476', '-0.3984', '-0.0782', '-0.1378', '-0.09534', '-0.1337', '0.05792', '-0.09906', '-0.09247', '-0.2483', '0.0565', '0.1924', '0.0942', '0.071', '0.0664', '0.5', '0.934', '-0.002676', '0.5522', '-0.2275', '-0.2426', '0.3726', '0.1855', '0.42', '0.04712', '0.1218', '-0.2158', '0.2325', '0.656', '0.384', '0.3918', '-0.282', '-0.4495', '0.807', '0.57', '-0.0819', '0.532', '-0.414', '-0.1254', '0.1951', '-0.07654', '0.01383', '-0.1953', '1.021', '-0.10065', '-0.1732', '-0.52', '0.0995', '-1.06', '0.3901', '0.796', '-0.3308', '-0.00439', '0.1459', '0.1914', '0.0134', '-0.561', '0.1058', '-0.2332', '-0.1118', '-0.7397', '0.5674', '0.0806', '0.2559', '-0.326', '-0.1232', '0.7065']",C84706,,D004402,,,10039179,
mondo:0009132,dysautonomia-like disorder,"['dysautonomia like disorder', 'dysautonomia-like disorder']",,224000,,C1857153,,,,C535728,,,,
mondo:0009133,"cerebellar ataxia, intellectual disability, and dysequilibrium","['dialysis dysequilibrium syndrome', 'cerebellar ataxia, mental retardation, and dysequilibrium', 'cerebellar hypoplasia, VLDLR associated', 'dysequilibrium syndrome', 'CAMRQ syndrome', 'cerebellar disorder, nonprogressive, with mental retardation', 'DES', 'VLDLRCH', 'CAMRQ', 'cerebellar ataxia, mental retardation and dysequlibrium syndrome', 'cerebellar ataxia-intellectual disability-dysequilibrium syndrome syndrome', 'non-progressive cerebellar ataxia-intellectual disability syndrome']",0050997,,1766,,"['-0.9805', '-0.2148', '-0.0851', '-0.3193', '-0.231', '-0.2925', '-0.06934', '0.935', '-0.3691', '-0.1259', '0.04663', '0.12225', '-0.1247', '-0.478', '0.4968', '-0.3083', '0.4114', '0.1519', '0.1637', '-0.5986', '0.2058', '-0.06396', '-0.2306', '-0.479', '0.191', '-0.05136', '-0.1981', '-0.1299', '-0.02055', '-0.2231', '-0.05234', '-0.02147', '0.4685', '0.2135', '-0.2961', '0.06915', '0.08105', '-0.1818', '-0.459', '-0.2559', '-0.04532', '0.0748', '-0.0717', '-0.1486', '-1.365e-05', '-0.1509', '0.048', '0.389', '-0.00644', '-0.00351', '0.0446', '0.10864', '0.0956', '-0.257', '0.0583', '0.068', '0.3481', '-0.554', '-0.4302', '0.1511', '-0.08966', '0.3457', '0.512', '-0.312', '-0.4895', '-0.10266', '-0.1321', '0.2379', '-0.2124', '0.1266', '-0.4253', '0.5444', '0.010826', '-0.714', '0.5366', '0.1714', '0.7437', '0.007725', '-0.1361', '0.1643', '0.04886', '-0.08545', '0.1754', '0.603', '0.4927', '0.632', '-0.01895', '0.461', '0.1376', '0.163', '-0.10443', '0.4849', '-0.4897', '0.0978', '0.418', '0.303', '0.431', '0.05194', '0.3652', '0.4646']",C114781,,C535731,,,10013140,
mondo:0009134,congenital dyserythropoietic anemia type 2,"['CDA type II', 'hempas anemia', 'anemia, congenital dyserythropoietic, type II', 'Cda 2', 'hempas anaemia', 'anemia, dyserythropoietic, congenital type 2', 'CDA II', 'CDA type 2', 'dyserythropoietic anemia, congenital, type II', 'anemia, congenital dyserythropoietic, type 2', 'dyserythropoietic Anemia, congenital, type 2', 'dyserythropoietic Anemia, hempas type', 'congenital dyserythropoietic anemia type 2', 'hereditary erythroblastic multinuclearity with a positive acidified-serum test (hempas)', 'hereditary erythroblastic multinuclearity with Positive acidified-serum test', 'SEC23B-CDG', 'CDAN2']",0111401,224100,98873,,"['-0.4597', '0.4106', '-0.329', '0.3735', '0.307', '0.304', '-0.4834', '0.4375', '-0.205', '-0.6', '0.1687', '0.1222', '0.3523', '0.2201', '-1.05', '0.002125', '-0.745', '-0.01101', '-0.4163', '-0.5757', '-0.01139', '-0.601', '0.6094', '-0.0892', '0.589', '-0.2717', '-0.1278', '-0.263', '0.535', '0.2761', '0.0713', '0.09595', '0.4797', '0.6196', '0.3672', '-0.3425', '-0.9365', '-0.7', '0.7056', '-0.131', '-0.718', '0.251', '0.2303', '-0.45', '-0.4478', '-0.5654', '-0.000577', '0.2512', '0.4624', '-0.1764', '0.627', '0.5806', '0.9067', '-0.338', '0.4834', '-0.427', '0.1288', '0.1886', '-1.113', '0.10944', '0.1737', '0.336', '-0.0996', '-0.4827', '0.1824', '0.3325', '0.2524', '0.793', '-0.321', '1.0', '0.797', '-0.2458', '-0.514', '-0.5796', '0.258', '0.9233', '0.1359', '0.01299', '0.1017', '0.2307', '0.157', '0.015015', '-0.09735', '-0.02385', '0.1683', '-0.4568', '-0.602', '0.377', '0.6333', '-0.353', '0.436', '0.22', '-0.2583', '-0.1309', '0.7373', '0.9644', '0.0949', '0.4346', '0.4585', '-0.643']",,,,285.8,,,
mondo:0009135,"anemia, congenital dyserythropoietic, type 1a","['CDAN1A', 'anemia, congenital dyserythropoietic, type Ia', 'anemia, congenital dyserythropoietic, type 1', 'dyserythropoietic Anemia, congenital, type Ia', 'CDA Ia']",0111398,224120,,,,,,,,,,
mondo:0009136,"dyskeratosis congenita, autosomal recessive 1","['dyskeratosis congenita autosomal recessive', 'autosomal recessive dyskeratosis congenita', 'autosomal recessive dyskeratosis congenita 1', 'DKCB1', 'DKCB', 'dyskeratosis congenita, autosomal recessive 1', 'dyskeratosis congenita, autosomal recessive type 1']",0070015,224230,,C1857144,,C176925,,C565611,,,,
mondo:0009137,dysmyelination with jaundice,['dysmyelination with jaundice'],,224250,,C1857143,,,,C565610,,,,
mondo:0009138,dysosteosclerosis,['dysosteosclerosis'],,224300,1782,C0432262,,,,C562973,756.9,,,
mondo:0009139,"dyssegmental dysplasia, Rolland-Desbuquois type","['dyssegmental dwarfism, Rolland-Desbuquois type', 'dyssegmental dwarfism Rolland-Desbuquois type', 'Anisospondylic Camptomicromelic dwarfism, Rolland-Desbuquois type', 'dyssegmental dysplasia, Rolland-Desbuquois type', 'Ddrd', 'Anisospondylic camptomicromelic dwarfism Rolland-Desbuquois type', 'dyssegmental dysplasia Rolland-Desbuquois type']",,224400,156731,C0432209,,,,C537999,756.59,,,
mondo:0009140,Silverman-Handmaker type dyssegmental dysplasia,"['dyssegmental dwarfism, Silverman-Handmaker type', 'Anisospondylic camptomicromelic dwarfism Silverman-Handmaker type', 'DDSH', 'dyssegmental dysplasia, Silverman-Handmaker type', 'Anisospondylic Camptomicromelic dwarfism, Silverman-Handmaker type', 'dyssegmental dwarfism Silverman-Handmaker type', 'dyssegmental dysplasia Silverman-Handmaker type']",0090032,224410,1865,,"['-0.414', '-0.03363', '0.4058', '-0.7104', '0.00843', '-0.2133', '0.1192', '0.5264', '-0.638', '0.06696', '-0.5967', '0.02095', '-0.002264', '0.2544', '-0.426', '0.125', '0.2996', '0.01079', '-0.6064', '-0.728', '0.1093', '0.2455', '0.738', '-0.002073', '-0.1542', '0.1531', '-0.1433', '-0.18', '0.7256', '-0.724', '0.3325', '-0.1722', '0.5825', '0.369', '0.3557', '-0.1466', '-0.556', '-0.4514', '-0.1904', '-0.554', '-0.1034', '-0.1421', '0.1863', '0.2678', '-0.04645', '-0.4614', '0.11676', '0.7983', '-0.0257', '-0.11633', '-0.1217', '0.01347', '-0.1726', '-0.0206', '-1.004', '-0.84', '-0.5205', '-0.486', '0.1976', '-0.1055', '0.393', '-0.02733', '-0.569', '0.184', '-0.3218', '-0.02364', '0.4417', '0.2262', '-0.11804', '0.2524', '-0.3816', '0.1693', '0.3318', '-0.2712', '-0.3386', '-0.01846', '-0.2776', '0.1554', '-0.3613', '-0.454', '-0.06903', '0.1898', '-0.0834', '0.513', '-0.2478', '0.433', '0.1214', '0.4558', '0.7935', '0.1769', '0.03165', '0.01541', '0.0964', '0.4084', '0.672', '0.533', '1.099', '-0.076', '0.4817', '0.548']",,,C537998,759.89,,,
mondo:0009141,torsion dystonia 2,"['dystonia musculorum deformans 2', 'primary dystonia, DYT2 type', 'HPCA dystonic disorder', 'dystonia musculorum deformans type 2', 'DYT2', 'dystonia 2, torsion, autosomal recessive', 'dystonic disorder caused by mutation in HPCA', 'torsion dystonia type 2', 'autosomal recessive torsion dystonia 2', 'torsion dystonia 2, autosomal recessive type']",0090038,224500,99657,C1857093,"['0.5615', '0.07666', '-0.05438', '-0.3074', '-0.04773', '-1.278', '0.616', '0.2467', '-0.587', '-0.2218', '1.001', '0.7275', '-0.2793', '0.4304', '0.5283', '0.6895', '-0.0432', '-0.801', '-0.4375', '-1.113', '-0.572', '-0.244', '0.2101', '-0.2073', '-0.3503', '0.1821', '-0.3018', '0.3442', '-0.333', '0.01081', '0.4053', '0.08856', '0.8525', '-0.04468', '0.506', '0.06903', '0.7593', '-0.1578', '0.3958', '-0.3977', '0.3154', '0.01863', '-0.3735', '0.1744', '0.4846', '-0.1616', '-0.325', '0.11383', '0.5723', '0.4272', '-0.05255', '0.2197', '0.656', '0.01276', '0.5273', '-0.2795', '0.12213', '0.7847', '0.1698', '-0.3694', '-0.633', '-0.3704', '0.1581', '-0.566', '-0.973', '0.8438', '0.3118', '0.2493', '-0.2299', '0.3896', '-0.4673', '-0.3535', '0.2314', '-0.013855', '0.2883', '0.683', '0.962', '0.1053', '0.1804', '-0.2935', '-0.1384', '0.1067', '0.403', '0.4492', '0.9463', '-0.02507', '0.3606', '0.175', '1.512', '-0.0371', '0.3918', '-0.0543', '0.3633', '0.2242', '0.901', '0.01952', '-0.1703', '0.1628', '0.4841', '-0.1371']",C123415,,C538006,,,,
mondo:0009142,dystonia with Ringbinden,['dystonia with Ringbinden'],,224550,,C1857089,,,,C565608,,,,
mondo:0009143,Meier-Gorlin syndrome 1,"['microtia, absent patellae, micrognathia syndrome', 'ORC1 Meier-Gorlin syndrome', 'Meier-Gorlin syndrome 1', 'Meier-Gorlin syndrome', 'MGORS1', 'Ear, patella, short stature syndrome', 'Meier-Gorlin syndrome caused by mutation in ORC1', 'Meier-GORLIN syndrome 1', 'Meier-Gorlin syndrome type 1']",0080512,224690,,CN030358,,,,,759.89,,,
mondo:0009144,Ebstein anomaly,"['Ebstein anomaly (disease)', 'Ebstein^s anomaly of common atrioventricular valve', 'Ebstein anomaly of the tricuspid valve', 'Ebstein^s malformation', 'Ebstein^s anomaly (disorder) [ambiguous]', 'Ebstein^s anomaly of tricuspid valve', 'Ebstein malformation', 'Ebstein^s anomaly', 'Ebstein anomaly', 'Ebstein^s anomaly of right atrioventricular valve']",14289,224700,1880,C0013481,,C84681,0007244,D004437,746.2,,10014075,
mondo:0009145,SchC6pf-Schulz-Passarge syndrome,"['SChöPF-Schulz-Passarge syndrome', 'palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome', 'keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis', 'keratosis palmoplantaris-cystic eyelids-hypodontia-hypotrichosis syndrome', 'eccrine tumours with ectodermal dysplasia', 'palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypotrichosis syndrome', 'SSPS', 'SCHOPF-Schulz-Passarge syndrome', 'eccrine tumors-ectodermal dysplasia', 'eccrine tumors with ectodermal dysplasia']",0111647,224750,50944,C1857069,"['0.01994', '0.0591', '-0.05322', '-0.381', '0.1037', '-0.631', '0.1708', '0.144', '-0.2249', '-0.689', '-0.0846', '-0.0426', '-0.5933', '-0.3193', '-0.228', '0.2773', '0.07776', '-0.541', '0.0377', '-0.5083', '-0.632', '0.1043', '0.4387', '-0.0787', '0.2383', '0.4368', '-0.7935', '-0.1344', '-0.2074', '-0.6196', '0.588', '-0.391', '0.1747', '0.381', '0.3337', '0.01591', '-0.5215', '-0.2495', '-0.0338', '-0.3052', '0.1154', '-0.1892', '0.08264', '-0.0431', '0.579', '-0.3835', '-0.2041', '0.1494', '-0.2238', '-0.7397', '0.5234', '0.6953', '-0.3218', '0.587', '-0.105', '-0.4807', '0.7227', '-0.1478', '-0.4062', '-0.1694', '0.518', '-0.02368', '-0.096', '0.286', '0.0639', '0.03204', '0.648', '0.7524', '0.2482', '0.554', '-0.2411', '-0.2009', '0.1699', '0.2742', '0.4622', '-0.1008', '-0.2477', '-0.002213', '0.1726', '-0.2793', '0.1302', '0.6074', '-0.3667', '0.55', '-0.05243', '-0.5015', '-0.04095', '0.06073', '0.1721', '-0.0018215', '0.437', '0.1355', '0.3672', '0.2247', '0.78', '-0.1852', '0.5693', '-0.3584', '0.3887', '-0.06555']",,,C565607,758.89,,,
mondo:0009146,ectodermal dysplasia-sensorineural deafness syndrome,"['hidrotic ectodermal dysplasia, sensorineural hearing loss and contracture of the fifth fingers', 'ectodermal dysplasia and neurosensory deafness', 'ectodermal dysplasia-sensorineural hearing loss syndrome', 'congenital ectodermal dysplasia with hearing loss', 'Mikaelian syndrome']",,224800,1883,C1857068,,,,C565606,,,,
mondo:0009147,"ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive","['ectodermal dysplasia, hypohidrotic', 'ECTD10B', 'ectodermal dysplasia 10B, hypohidrotic/hair/tooth type, autosomal recessive', 'ectodermal dysplasia, anhidrotic']",0111665,224900,,C3887494,,,,,,,,
mondo:0009148,Rosselli-Gulienetti syndrome,['Rosselli-Gulienetti syndrome'],,225000,90339,C0796139,,,,C563117,,,,
mondo:0009149,ectodermal dysplasia-intellectual disability-central nervous system malformation syndrome,"['ectodermal dysplasia, hypohidrotic, with hypothyroidism and agenesis of the corpus callosum']",,225040,1812,C1857053,,,,C565605,,,,
mondo:0009150,hypohidrotic ectodermal dysplasia-hypothyroidism-ciliary dyskinesia syndrome,"['another syndrome', 'ectodermal dysplasia hypohidrotic with hypothyroidism and ciliary dyskinesia', 'hypohidrotic ectodermal dysplasia with hypothyroidism and ciliary dyskinesia', 'ectodermal dysplasia, hypohidrotic, with hypothyroidism and ciliary dyskinesia', 'hypohidrotic ectodermal dysplasia with hypothyroidism', 'HEDH syndrome', 'hypohidrotic ectodermal dysplasia - hypothyroidism - ciliary dyskinesia']",,225050,1882,,,,,C565604,,,,
mondo:0009151,cleft lip/palate-ectodermal dysplasia syndrome,"['CLPED1', 'Zlotogora-Zilberman-Tenenbaum syndrome', 'cleft lip/palate-ectodermal dysplasia syndrome', 'cleft lip/palate-syndactyly-pili torti syndrome', 'ectodermal dysplasia type 4', 'ectodermal dysplasia, margarita Island type', 'ectodermal dysplasia, cleft lip and palate, mental retardation, and syndactyly', 'ectodermal dysplasia margarita island type', 'autosomal recessive ectodermal dysplasia', 'CLEPD', 'syndactyly-ectodermal dysplasia-cleft/lip palate', 'cleft lip with or without cleft palate, nonsyndromic, 7', 'Zlotogora syndrome', 'cleft lip-palate-ectodermal dysplasia syndrome', 'orofacial cleft 7', 'cleft lip/palate-syndactyly-pili torti', 'Bustos Simosa pinto Cisternas syndrome', 'ectodermal dysplasia, type 4', 'ED4', 'margarita type of ectodermal dysplasia', 'Zlotogora-Ogur syndrome', 'ectodermal dysplasia, cleft lip and palate, intellectual disability, and syndactyly']",0060773,225060,3253,CN229116,"['0.0964', '-0.148', '0.3213', '-0.5083', '0.5557', '-0.3386', '0.2686', '0.4507', '-0.0912', '-0.5933', '0.11127', '-0.202', '-0.5186', '0.03616', '-0.3394', '0.423', '0.4185', '-0.2123', '-0.12134', '-0.588', '0.05234', '0.0808', '0.3171', '-0.2942', '0.3923', '0.1478', '-0.5845', '0.10706', '0.2413', '-0.6416', '0.698', '-0.4456', '-0.0956', '-0.06247', '0.0878', '0.0866', '0.1736', '-0.114', '0.08777', '-0.3655', '0.3098', '-0.1432', '-0.2048', '-0.2083', '0.08905', '-0.289', '0.11255', '0.2573', '0.1367', '-0.1779', '-0.09283', '-0.3528', '-0.07104', '0.4517', '-0.889', '0.0919', '0.631', '-0.502', '-0.3066', '-0.00978', '0.328', '0.3542', '-0.463', '-0.2979', '0.4258', '-0.1855', '-0.2512', '0.2369', '-0.1631', '0.4282', '-0.4978', '-0.2119', '-0.010574', '0.1377', '-0.0657', '0.3577', '0.08203', '-0.1702', '-0.1211', '0.2534', '-0.0281', '-0.00821', '0.5034', '0.3176', '0.10693', '-0.04495', '-0.281', '0.8887', '-0.0248', '0.6084', '-0.2158', '0.3665', '0.3333', '0.3179', '0.9507', '-0.1329', '0.57', '-0.657', '0.4639', '0.3328']",C122656,,,,,,
mondo:0009152,"ectopia lentis 2, isolated, autosomal recessive","['autosomal recessive isolated ectopia lentis 2', 'ectopia lentis, isolated autosomal recessive', 'ectopia lentis, isolated, autosomal recessive', 'ECTOL2', 'autosomal recessive isolated ectopia lentis', 'ectopia lentis 2, isolated, autosomal recessive']",0111149,225100,,C3541474,,,,,,,,
mondo:0009153,ectopia lentis et pupillae,"['ectopia lentis with ectopia of pupil', 'ectopia lentis et pupillae']",0111648,225200,,C1644196,,,,C563268,,,,
mondo:0009154,"hypothyroidism, congenital, nongoitrous, 5","['hypothyroidism, congenital, nongoitrous, 5', 'hypothyroidism, congenital, nongoitrous, type 5', 'hypothyroidism, congenital nongoitrous, 5', 'CHNG5', 'congenital nongoitrous hypothryoidism 5', 'NKX2-5 hypothyroidism, congenital, nongoitrous', 'congenital nongoitrous hypothyroidism 5', 'hypothyroidism, congenital, nongoitrous caused by mutation in NKX2-5']",0070125,225250,90673,C2673630,,,,C567123,,,,
mondo:0009155,EEM syndrome,"['EEM syndrome', 'ectodermal dysplasia, ectrodactyly, and macular dystrophy syndrome', 'EEMS', 'ectodermal dysplasia, ectrodactyly, and macular dystrophy', 'ectodermal dysplasia-ectrodactyly-macular dystrophy syndrome']",0111649,225280,1897,,"['-0.163', '-0.1427', '0.10065', '-0.2676', '0.613', '-0.326', '-0.2937', '0.343', '-0.0634', '-1.008', '-0.07874', '-0.1774', '-0.655', '-0.311', '-0.1798', '0.1632', '0.5786', '-0.4185', '-0.3687', '-0.479', '-0.2012', '-0.02399', '0.2198', '0.08356', '0.06464', '0.2272', '-0.2426', '0.113', '0.5024', '0.10547', '0.6016', '-0.629', '-0.3787', '0.0677', '0.3728', '0.2893', '0.04413', '-0.4128', '0.0007424', '-0.2551', '-0.06104', '-0.4497', '0.03934', '-0.434', '-0.06247', '-0.2512', '0.00516', '0.0997', '-0.04495', '-0.6577', '0.11725', '-0.1489', '0.1958', '0.2732', '-0.00234', '-0.443', '0.7686', '-0.11163', '-0.6704', '-0.231', '-0.3384', '0.1774', '0.2009', '0.339', '-0.1656', '-0.00858', '0.4026', '0.7173', '-0.2478', '0.2267', '-0.2448', '-0.2223', '-0.006866', '0.2085', '0.138', '0.1056', '-0.01326', '0.00498', '0.0637', '-0.342', '0.4749', '0.2299', '0.716', '0.9604', '-0.12213', '-0.205', '-0.12006', '0.4236', '0.2554', '0.4143', '-0.03064', '0.617', '0.6025', '0.374', '0.867', '-0.1757', '0.2441', '-0.2795', '-0.04086', '0.1971']",,,C536190,,,,
mondo:0009156,ectrodactyly-polydactyly syndrome,"['ectrodactyly-polydactyly', 'ectrodactyly polydactyly']",,225290,1892,C1857040,,,,C565601,,,,
mondo:0009157,split hand-foot malformation 6,"['ectrodactyly, autosomal recessive', 'split hand-foot malformation caused by mutation in WNT10B', 'split hand-foot malformation type 6', 'split-hand/foot malformation 6', 'WNT10B split hand-foot malformation', 'SHFM6', 'split-hand/foot malformation type 6']",0090026,225300,,C2749665,,,,C567616,,,,
mondo:0009158,"Ehlers-Danlos syndrome, fibronectinemic type","['Ehlers-Danlos syndrome, type 10', 'EDS 10', 'EDS10 (formerly)', 'Ehlers-Danlos syndrome with platelet dysfunction from fibronectin abnormality', 'Ehlers-Danlos syndrome, type X (formerly)', 'Ehlers-Danlos syndrome, fibronectin-deficient', 'Ehlers-Danlos syndrome, dysfibronectinemic type', 'Ehlers-Danlos syndrome type 10 (formerly)', 'FN Abnormality', 'EDS X', 'Ehlers-Danlos syndrome type 10']",,225310,75501,,,,,C565600,,,,
mondo:0009159,"Ehlers-Danlos syndrome, cardiac valvular type","['Cardiac valvular form of Ehlers-Danlos syndrome', 'EDS, cardiac valvular type', 'Ehlers-Danlos syndrome, arthrochalasis type', 'cvEDS', 'Cardiac-valvular EDS', 'Ehlers-Danlos syndrome, CARDIAC valvular type', 'Ehlers-Danlos syndrome, autosomal recessive, CARDIAC valvular form', 'Ehlers-Danlos syndrome, autosomal recessive, Cardiac valvular form', 'EDSCV', 'Cardiac-valvular Ehlers-Danlos syndrome', 'Cardiac valvular form of autosomal recessive Ehlers-Danlos syndrome']",0080730,225320,230851,,"['0.2769', '-0.03079', '-0.5195', '-0.1365', '0.337', '-0.652', '0.1829', '0.4714', '-0.7373', '0.7173', '0.09283', '-0.2368', '0.1843', '1.009', '-0.5684', '0.1921', '-0.7603', '0.4688', '-0.1401', '-0.3958', '0.1306', '1.105', '0.5396', '0.2769', '-0.4033', '0.3386', '0.1465', '0.03378', '1.395', '0.4475', '1.06', '-0.1774', '0.0944', '0.0398', '0.01549', '-0.07965', '-0.4773', '0.03111', '0.312', '-1.251', '1.024', '-0.3755', '-0.742', '0.1155', '-0.0327', '-0.4485', '-0.4324', '0.725', '0.8076', '-0.3582', '0.1672', '-0.432', '0.8013', '-0.02026', '0.105', '-0.585', '-0.3916', '0.825', '0.2147', '-0.00965', '0.1278', '0.6133', '0.1975', '-0.1931', '0.08923', '0.01875', '-0.2793', '0.99', '-0.3853', '1.005', '-0.895', '-0.0202', '-0.5376', '-0.309', '-0.12274', '-0.348', '-0.3206', '-0.03854', '-0.00741', '-0.10815', '-0.2374', '-0.5273', '0.3333', '0.631', '-0.7397', '0.02522', '0.02109', '0.812', '-0.05594', '-0.0853', '0.7715', '0.2285', '-0.3726', '0.584', '0.921', '0.07965', '0.9287', '-0.2698', '0.3093', '-0.01029']",,,C536200,,,,
mondo:0009161,"Ehlers-Danlos syndrome, dermatosparaxis type","['Ehlers-Danlos syndrome, type VII, autosomal recessive', 'EDSDERMS', 'dermatosparaxis Ehlers-Danlos syndrome', 'Ehlers-Danlos syndrome type 7C', 'Ehlers-Danlos syndrome type 7C (formerly)', 'dermatosparaxis', 'dermatosparaxis EDS', 'EDS7C', 'Ehlers-Danlos syndrome, dermatosparaxis type', 'dEDS', 'EDS VIIC', 'EDS 7C']",0080733,225410,1901,,"['0.341', '0.2051', '-0.4883', '0.03174', '0.292', '-0.7817', '-0.02806', '0.3735', '-0.925', '0.605', '0.0754', '-0.159', '0.2847', '1.149', '-0.565', '0.3757', '-0.634', '0.579', '0.05084', '-0.622', '-0.00457', '0.913', '0.477', '-0.04446', '-0.4329', '0.2283', '0.1586', '-0.11475', '1.463', '0.387', '1.262', '-0.502', '0.212', '-0.04736', '0.04828', '0.10657', '-0.4658', '-0.10474', '0.2347', '-1.072', '0.7104', '-0.5107', '-0.685', '-0.07263', '0.2627', '-0.4238', '-0.1964', '0.7197', '0.927', '-0.4277', '0.1611', '-0.3796', '0.7427', '-0.01242', '0.06076', '-0.4053', '-0.5347', '0.719', '0.318', '0.06073', '0.23', '0.441', '0.1383', '-0.2952', '0.003117', '0.1577', '-0.2786', '0.7607', '-0.2864', '1.118', '-0.628', '0.2485', '-0.594', '-0.4062', '-0.23', '-0.1973', '-0.4094', '0.1581', '0.1694', '-0.221', '-0.3562', '-0.4487', '0.3284', '0.7515', '-0.6353', '-0.184', '0.0673', '0.8423', '0.2798', '0.01213', '0.684', '0.49', '-0.5576', '0.5664', '0.881', '-0.04248', '0.578', '-0.4512', '0.1587', '-0.01631']",,,C567527,,,,
mondo:0009162,Ellis-van Creveld syndrome,"['EVC', 'Mesoectodermal dysplasia', 'Chondroectodermal dysplasia', 'Ellis-VAN Creveld syndrome', 'Ellis-van Creveld syndrome', 'mesodermic dysplasia', 'Ellis Van Creveld syndrome']",12714,225500,289,CN239258,"['0.0752', '0.2001', '0.48', '-0.2976', '0.4583', '-0.3281', '0.322', '1.375', '-0.1438', '-0.4504', '-0.315', '-0.09595', '0.2026', '0.2688', '-0.1543', '0.1843', '0.261', '0.02254', '-0.6587', '-0.7524', '0.04968', '0.3352', '0.4717', '-0.5425', '-0.2556', '-0.587', '-0.5283', '0.2961', '0.693', '-0.4006', '0.3838', '-0.1257', '-0.295', '-0.2683', '0.1078', '-0.0898', '0.3508', '-0.538', '0.09845', '0.1298', '0.2327', '0.2344', '0.5366', '-0.2473', '-0.1615', '-0.3389', '-0.1925', '0.621', '0.09094', '-0.1433', '-0.01686', '0.04343', '-0.0668', '-0.1096', '-0.4814', '-0.4624', '-0.1736', '-0.04462', '0.04904', '-0.2078', '0.1534', '0.2222', '-0.2585', '0.2815', '-0.2007', '-0.0468', '-0.0721', '0.594', '-0.63', '0.2072', '-0.1912', '-0.3608', '0.1401', '0.0993', '-0.02779', '0.1287', '0.1359', '-0.4395', '-0.5405', '-0.326', '0.15', '-0.09357', '-0.2163', '0.2362', '0.02335', '0.3352', '0.709', '0.04065', '-0.05118', '0.2234', '0.2542', '-0.2737', '-0.0842', '0.462', '0.3513', '-0.1915', '0.4128', '-0.4802', '0.2773', '0.02022']",C84684,,D004613,756.55,,10008724,
mondo:0009163,"encephalomalacia, multilocular","['encephalomalacia, multilocular']",,225700,,C1856991,,,,C565597,,,,
mondo:0009164,"encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts","['Lyon syndrome', 'encephalopathy, axonal, with necrotizing myopathy, cardiomyopathy, and cataracts']",,225740,,C1856990,,,,C565596,,,,
mondo:0009165,Aicardi-Goutieres syndrome 1,"['Aicardi-Goutieres syndrome caused by mutation in TREX1', 'Aicardi-Goutieres syndrome type 1', 'Cree encephalitis', 'TREX1 Aicardi-Goutieres syndrome', 'Aicardi-Goutieres syndrome 1, autosomal dominant', 'Pseudotoxoplasmosis syndrome', 'AGS1', 'Aicardi-Goutieres syndrome 1', 'Aicardi-Goutieres syndrome 1, dominant and recessive', 'Ags', 'encephalopathy, familial infantile, with intracranial calcification and chronic cerebrospinal fluid lymphocytosis']",,225750,,C0796126,,C165501,,,,,,
mondo:0009166,pontocerebellar hypoplasia type 4,"['encephalopathy, fatal infantile, with olivopontocerebellar Hypoplasia', 'olivopontocerebellar hypoplasia', 'fatal infantile encephalopathy with olivopontocerebellar hypoplasia', 'encephalopathy fatal infantile with olivopontocerebellar hypoplasia', 'PCH4', 'pontocerebellar hypoplasia, type 4']",0060273,225753,166063,C1856974,"['-0.2467', '0.279', '-0.612', '-0.04892', '0.4988', '-0.783', '0.0569', '0.7646', '-1.276', '-0.348', '-0.3853', '-0.199', '-0.3574', '-0.759', '0.01686', '-0.453', '0.5513', '-0.207', '-0.2129', '-0.8354', '0.02388', '-0.495', '0.3174', '-0.633', '0.0928', '0.3643', '-0.79', '0.185', '0.2346', '-0.21', '0.1087', '0.601', '0.4385', '-0.1755', '-0.1353', '-0.3374', '0.221', '-0.01985', '0.1334', '0.1831', '-0.2834', '-0.03152', '0.3218', '-0.263', '-0.5557', '0.0337', '-0.4788', '0.2346', '0.1378', '0.1859', '0.2064', '-0.7065', '-0.4111', '-0.003729', '-0.1763', '-0.6553', '0.2751', '0.05383', '0.2142', '0.6665', '0.1134', '0.1824', '0.3145', '0.4224', '-0.0166', '-0.562', '0.3645', '0.268', '-0.7793', '0.1492', '-0.03833', '0.1327', '0.5957', '0.349', '0.1627', '-0.1759', '0.2373', '-0.4343', '-1.049', '-0.09686', '-0.1604', '0.4082', '0.1968', '0.73', '0.1581', '0.575', '0.4592', '0.314', '0.5366', '-0.1484', '0.0943', '0.1202', '-0.0941', '0.26', '0.2869', '0.517', '1.107', '-0.4932', '1.3', '0.3743']",,,C536716,,,,
mondo:0009167,Bonnemann-Meinecke-Reich syndrome,"['encephalopathy intracranial calcification growth hormone deficiency microcephaly retinal degeneration', 'encephalopathy-intracerebral calcification-retinal degeneration syndrome', 'encephalopathy with intracranial calcification, growth hormone deficiency, microcephaly, and retinal degeneration', 'Bonnemann Meinecke Reich syndrome']",,225755,1261,C1856973,,,,C565594,,,,
mondo:0009168,Fowler syndrome,"['hydranencephaly, fowler type', 'cerebral proliferative glomeruloid vasculopathy', 'proliferative vasculopathy and hydranencephaly/hydrocephaly', 'PVHH', 'hydrocephaly/hydranencephaly due to cerebral vasculopathy', 'Encephaloclastic proliferative vasculopathy', 'proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome']",0111666,225790,221126,,"['-0.3477', '0.1164', '0.0648', '-0.3367', '-0.298', '-0.1996', '-0.0882', '0.3555', '-0.2588', '0.0527', '-0.27', '-0.1997', '-0.01535', '-0.06287', '-0.1296', '-0.263', '0.1926', '0.3672', '-0.2433', '-0.509', '-0.001754', '-0.1583', '0.28', '-0.2878', '-0.02455', '-0.0708', '-0.1348', '0.04703', '0.1195', '-0.02628', '0.3103', '-0.2207', '0.6743', '0.258', '0.0432', '0.03003', '0.00963', '-0.2417', '-0.11', '0.1277', '0.2021', '-0.04242', '-0.05026', '-0.1087', '-0.2144', '-0.1981', '-0.09106', '0.0547', '-0.0856', '0.3906', '-0.1619', '0.2786', '-0.0947', '-0.10803', '-0.2737', '-0.01061', '0.2284', '-0.3894', '0.1757', '0.10547', '0.3286', '0.04974', '0.1813', '-0.01483', '-0.2085', '-0.107', '0.1875', '0.3162', '-0.4163', '0.235', '0.05304', '0.1398', '-0.1564', '0.2267', '-0.1594', '-0.2396', '0.2976', '0.2394', '-0.392', '0.0448', '-0.0612', '0.2083', '0.1471', '0.341', '-0.00997', '-0.1367', '0.3354', '0.2615', '0.12494', '0.0348', '0.2102', '0.412', '0.1897', '0.0762', '0.546', '0.084', '0.3457', '-0.446', '0.3862', '-0.0671']",,,C565593,596.59,,10071718,
mondo:0009169,endocardial fibroelastosis,"['endocardial fibroelastosis', 'Elastomyofibrosis', 'EFE', 'endomyocardial fibroelastosis']",12929,226000,2022,C0014117,,C98922,0007251,D004695,425.3,I42.4,10014663,
mondo:0009170,endocardial fibroelastosis and coarctation of abdominal aorta,['endocardial fibroelastosis and coarctation of abdominal aorta'],,226100,,C1856971,,,,C565592,,,,
mondo:0009171,"endothelial dystrophy, congenital hereditary, with nail hypoplasia","['endothelial dystrophy, congenital hereditary, with nail hypoplasia']",,226110,,C1856970,,,,C565591,,,,
mondo:0009172,enterocolitis,"['enterocolitis (disease)', 'enterocolitis']",,226150,,C0014356,,C79573,1001481,D004760,558.9,,,0004387
mondo:0009173,congenital enteropathy due to enteropeptidase deficiency,"['congenital enterokinase deficiency', 'enterokinase deficiency', 'enteropeptidase deficiency']",0111667,226200,168601,C0268416,"['-0.357', '0.1526', '0.103', '-0.11456', '0.1315', '-0.075', '-0.0895', '0.1348', '-0.05383', '0.05243', '0.1339', '0.02939', '-0.04868', '-0.02017', '-0.4568', '-0.1732', '0.1499', '0.1516', '-0.3015', '-0.705', '0.0753', '-0.3462', '0.2834', '-0.058', '-0.01709', '-0.06635', '-0.00172', '0.0788', '0.1627', '-0.3274', '0.1576', '0.10547', '0.4019', '0.3577', '-0.02522', '-0.1447', '-0.319', '0.1476', '-0.06027', '0.004288', '-0.236', '-0.09937', '0.1371', '-0.0526', '-0.1453', '-0.2471', '0.0679', '0.0204', '0.1707', '0.2164', '-0.2651', '0.05237', '0.2328', '-0.1562', '-0.2524', '0.0372', '0.01256', '-0.363', '-0.3806', '0.002014', '0.295', '0.1638', '-0.02185', '-0.3254', '0.2783', '0.02856', '0.2527', '0.0729', '-0.2219', '0.1719', '-0.2162', '-0.02481', '0.03967', '-0.2125', '0.02939', '-0.1636', '0.3396', '-0.0477', '-0.05884', '0.2358', '-0.2262', '-0.1637', '-0.08234', '0.07336', '0.1954', '-0.0614', '0.08246', '0.0149', '0.265', '-0.06082', '0.2627', '0.1932', '-0.08484', '0.03397', '0.4482', '0.3328', '0.194', '-0.2456', '0.119', '0.2676']",,,C562649,277.89,,,
mondo:0009174,protein-losing enteropathy,"['protein-losing enteropathy', 'complement hyperactivation, ANGIOPATHIC thrombosis, and PROTEIN-losing enteropathy', 'CHAPLE', 'exudative enteropathy', 'enteropathy, exudative', 'complement hyperactivation, Angiopathic thrombosis, and Protein-losing enteropathy', 'enteropathy, PROTEIN-losing', 'protein-losing enteropathy (disease)']",10611,226300,566175,C0033680,,,,D011504,579.8,,,0002243
mondo:0009175,eosinophilic fasciitis,"['diffuse fasciitis with eosinophilia', 'EF', 'eosinophilic fasciitis (disease)', 'Shulman syndrome', 'eosinophilic fasciitis']",,226350,3165,C0264005,,C112116,,C562487,728.89,,10014954,0045029
mondo:0009176,epidermodysplasia verruciformis,"['epidermodysplasia verruciformis', 'Lewandowsky-Lutz dysplasia', 'ever', 'Lewandowsky-Lutz syndrome', 'Lutz-Lewandowsky epidermodysplasia verruciformis', 'EV']",13777,,302,C0014522,"['0.5107', '0.06757', '-0.4058', '-0.2708', '0.2844', '-0.3699', '0.1387', '0.006393', '-0.2603', '-0.2563', '-0.1931', '0.3208', '-0.00441', '0.1824', '-0.4646', '0.058', '0.459', '-0.4263', '0.002998', '-0.2225', '-0.599', '-0.313', '0.2822', '-0.704', '-0.06683', '0.267', '-0.06976', '0.02403', '-0.2487', '-0.482', '0.5054', '-0.1002', '0.1317', '-0.213', '0.02063', '0.0567', '-0.03442', '-0.4143', '-0.1292', '0.1681', '-0.1809', '-0.3064', '0.7627', '-0.27', '0.3643', '-0.2017', '-0.2827', '0.1112', '0.1418', '-0.2666', '-0.2883', '-0.1503', '-0.09186', '0.4329', '-0.747', '0.3015', '0.645', '-0.2854', '-0.7026', '-0.2573', '0.01624', '0.3062', '-0.7593', '0.1046', '0.03864', '0.55', '0.46', '0.55', '0.4587', '0.7446', '-0.05484', '-0.569', '-0.02368', '0.4185', '0.667', '0.4495', '-0.3608', '-0.3975', '-0.2986', '0.03522', '-0.10266', '-0.2455', '0.125', '-0.05768', '-0.01857', '-0.509', '0.0002315', '0.2463', '0.2842', '0.2123', '0.1553', '0.04312', '-0.2281', '-0.0715', '0.5806', '-0.0661', '0.6973', '-0.5786', '-0.1421', '-0.4048']",C126877,,D004819,757.8,,10052339,
mondo:0009177,late-onset localized junctional epidermolysis bullosa-intellectual disability syndrome,"['epidermolysis bullosa simplex localisata associated with anodontia, hair and nail disorders', 'epidermolysis bullosa, late-onset localised junctional, with intellectual disability', 'epidermolysis bullosa, late-onset localized junctional, with intellectual disability', 'epidermolysis bullosa, late-onset localized junctional, with mental retardation', 'epidermolysis bullosa, late-onset localised junctional, with mental retardation']",,226440,231556,C1856969,,,,C535492,,,,
mondo:0009178,epidermolysis bullosa dystrophica Neurotrophica,"['epidermolysis bullosa dystrophica Neurotrophica', 'epidermolysis bullosa with congenital deafness', 'epidermolysis bullosa progressiva, recessive']",,226500,,,,,,C562637,757.39,,,
mondo:0009179,recessive dystrophic epidermolysis bullosa,"['epidermolysis bullosa dystrophica, Hallopeau-Siemens type', 'severe generalised recessive dystrophic epidermolysis bullosa', 'autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type', 'recessive dystrophic epidermolysis bullosa, severe generalised', 'RDEB, severe generalized', 'epidermolysis bullosa dystrophica inversa, autosomal recessive', 'autosomal recessive dystrophic epidermolysis bullosa generalisata gravis', 'epidermolysis bullosa dystrophica, generalized severe, autosomal recessive', 'RDEB, severe generalised', 'severe generalized RDEB', 'dystrophic epidermolysis bullosa, autosomal recessive', 'RDEB-sev gen', 'severe generalised RDEB', 'RDEB, Hallopeau-Siemens type', 'epidermolysis bullosa dystrophica, autosomal recessive', 'epidermolysis bullosa dystrophica, autosomal recessive, Localisata variant', 'epidermolysis bullosa dystrophica, autosomal recessive, modifier of', 'autosomal recessive dystrophic epidermolysis bullosa, Hallopeau-Siemens type (formerly)', 'recessive dystrophic epidermolysis bullosa, severe generalized', 'epidermolysis bullosa dystrophica, generalised severe, autosomal recessive', 'RDEB', 'severe generalized recessive dystrophic epidermolysis bullosa', 'RDEB generalisata gravis', 'epidermolysis bullosa dystrophica, AR', 'EBD inversa']",0060642,226600,79408,,"['0.003252', '0.03754', '-0.02448', '0.01495', '0.02675', '-0.05496', '-0.005787', '0.01964', '-0.001538', '-0.00894', '-0.03674', '-0.006172', '-0.0241', '0.01675', '-0.02306', '-0.01081', '0.02696', '-0.04282', '-0.01584', '-0.0855', '-0.008354', '-0.007484', '0.02882', '-0.001532', '0.0351', '0.001347', '-0.002592', '0.013115', '-0.0016985', '-0.04926', '0.003757', '-0.02736', '0.02567', '0.04144', '-0.005157', '-0.0012245', '-0.02904', '0.005215', '0.001868', '-0.05072', '0.01299', '-0.073', '0.009796', '-0.01683', '-0.03232', '-0.0514', '-0.02567', '0.02957', '-0.001514', '0.01118', '0.005074', '-0.02577', '0.02841', '0.007305', '-0.03476', '-0.01988', '0.0558', '0.01772', '-0.03072', '-0.01674', '0.0344', '-0.00915', '-0.002287', '-0.00492', '0.01944', '-0.02545', '0.05008', '0.02272', '-0.04266', '0.03955', '-0.03918', '-0.014496', '0.007732', '-0.00684', '0.01134', '0.003613', '0.02548', '-0.01043', '-0.006493', '-0.00705', '-0.007835', '0.01029', '-0.0139', '0.010895', '-0.02118', '0.002583', '-0.01491', '0.0377', '0.0103', '-0.00885', '0.00203', '0.05566', '0.014824', '0.01184', '0.08075', '0.02528', '0.03436', '-0.05972', '0.00276', '0.00847']",,,,757.39,,,
mondo:0009180,"junctional epidermolysis bullosa, non-Herlitz type","['epidermolysis bullosa, generalized atrophic benign', 'epidermolysis bullosa Junctionalis, Disentis type', 'JEB-I', 'epidermolysis bullosa Junctionalis, non-Herlitz type', 'JEB-nH', 'epidermolysis bullosa Junctionalis, progressive', 'epidermolysis bullosa, generalised atrophic benign', 'epidermolysis bullosa, junctional, Localisata variant', 'junctional epidermolysis bullosa inversa', 'epidermolysis bullosa, junctional, non-Herlitz type', 'epidermolysis bullosa Junctionalis, severe Nonlethal', 'JEN-nH']",,226650,89840,C2673610,"['0.608', '-0.3184', '-0.207', '-0.03552', '-0.03857', '-0.6025', '-0.521', '0.508', '-0.1439', '-0.682', '0.4707', '-0.4788', '-0.9204', '0.3599', '-0.6787', '0.01999', '0.2495', '-1.013', '-0.351', '-0.959', '-0.2488', '-0.23', '0.6704', '0.607', '0.5093', '0.295', '-1.117', '0.7583', '-0.2181', '-1.106', '0.2402', '-0.04446', '-0.3975', '-0.02818', '-0.0383', '0.1063', '-1.176', '0.1735', '1.252', '-0.6914', '0.1404', '-0.792', '0.1694', '0.04312', '0.1694', '-0.233', '-0.4634', '0.0952', '0.6', '-0.08966', '-0.509', '-0.7563', '0.668', '-0.01234', '-0.0897', '-0.5396', '-0.1654', '1.105', '-0.931', '-0.2983', '-0.02841', '0.4724', '-0.11945', '0.3835', '0.879', '0.8823', '0.258', '0.1448', '-0.824', '0.2766', '-0.1713', '-0.02582', '-0.4487', '0.01242', '0.0455', '-0.01622', '-0.12006', '0.2223', '0.02795', '-0.2012', '-1.002', '-0.09607', '-0.3027', '-0.1514', '0.2081', '0.229', '-1.215', '0.7812', '1.122', '0.3948', '-0.3801', '0.4502', '-0.02028', '0.5024', '-0.0894', '0.837', '0.2798', '-0.708', '0.8', '0.04276']",,,,757.39,,,
mondo:0009181,"epidermolysis bullosa simplex 5B, with muscular dystrophy","['Epidermolysa bullosa simplex and limb girdle muscular dystrophy', 'MD-EBS', 'Epidermolysa bullosa simplex with muscular dystrophy', 'EBS-MD', 'epidermolysis bullosa simplex with muscular dystrophy', 'limb-girdle muscular dystrophy with epidermolysis bullosa simplex', 'epidermolysis bullosa simplex - limb girdle muscular dystrophy', 'MDEBS', 'epidermolysis bullosa simplex and limb-girdle muscular dystrophy', 'EBSMD', 'epidermolysis bullosa simplex 5B, with muscular dystrophy']",0090017,226670,257,C2931072,"['0.7417', '-0.12067', '-0.3374', '-0.08154', '-0.2048', '-0.7837', '-0.527', '0.6274', '-0.063', '-0.7573', '0.2798', '-0.6006', '-0.7847', '0.2098', '-0.544', '0.2905', '0.2283', '-0.9727', '-0.4685', '-0.983', '-0.2035', '-0.3076', '0.2365', '0.721', '0.271', '0.0134', '-1.0205', '0.7847', '-0.5034', '-0.7095', '-0.1081', '-0.2852', '-0.4026', '0.02512', '0.0553', '0.03372', '-1.151', '0.2281', '1.066', '-0.7617', '0.3083', '-0.3958', '0.2202', '0.1526', '-0.00593', '-0.209', '-0.4487', '0.31', '0.2489', '-0.2499', '-0.3184', '-0.456', '0.635', '-0.03745', '0.1875', '-0.5405', '-0.1605', '0.9663', '-0.6465', '-0.1864', '0.0421', '0.4487', '-0.0762', '0.288', '0.905', '0.5913', '0.164', '0.3706', '-0.6387', '0.2031', '-0.1142', '-0.05103', '-0.04742', '0.01993', '0.1913', '0.05896', '0.0711', '0.16', '0.0362', '-0.208', '-0.759', '0.2507', '-0.2223', '-0.1884', '0.292', '0.3528', '-0.906', '0.723', '0.9956', '0.11163', '-0.4675', '0.235', '0.1741', '0.665', '-0.09436', '0.8184', '0.5054', '-0.3452', '0.718', '0.03818']",,,C535955,,,,
mondo:0009182,junctional epidermolysis bullosa Herlitz type,"['junctional epidermolysis bullosa, Herlitz type', 'epidermolysis bullosa, junctional, Herlitz-Pearson type', 'junctional epidermolysis bullosa, Herlitz-Pearson type', 'junctional epidermolysis bullosa, generalised severe', 'junctional epidermolysis bullosa, generalized severe', 'epidermolysis bullosa Junctionalis, Herlitz type', 'JEB-H', 'JEB-Herlitz type', 'junctional epidermolysis bullosa generalisata gravis', 'epidermolysis bullosa, junctional, Herlitz type', 'Herlitz-Pearson type epidermolysis bullosa', 'JEB, generalised severe', 'Herlitz-Pearson-type epidermolysis bullosa', 'Herlitz type epidermolysis bullosa junctionalis', 'JEB, generalized severe', 'epidermolysis bullosa letalis']",0060737,226700,79404,,"['0.811', '0.1946', '-0.4978', '0.1453', '0.10675', '-0.443', '-0.3125', '0.615', '-0.2632', '-0.7017', '0.1791', '-0.2332', '-0.828', '0.3884', '-0.71', '0.04584', '-0.1952', '-1.045', '-0.2103', '-0.63', '-0.2041', '-0.1219', '0.5425', '0.499', '0.1764', '0.5034', '-0.79', '0.719', '-0.2208', '-0.767', '0.3125', '-0.2556', '-0.3267', '-0.10254', '0.02946', '0.0881', '-1.102', '0.1915', '1.038', '-0.5435', '0.2698', '-0.61', '0.0493', '-0.1334', '-0.0505', '-0.0847', '-0.2595', '0.03049', '0.3782', '-0.02875', '-0.647', '-0.752', '0.595', '-0.2096', '0.00286', '-0.4202', '-0.2505', '1.157', '-0.7056', '-0.184', '-0.2534', '0.3792', '-0.2534', '0.513', '1.151', '0.6187', '0.4583', '0.1809', '-0.704', '0.295', '-0.0629', '0.04892', '-0.4592', '-0.1897', '-0.136', '0.11584', '0.2242', '0.1221', '-0.1414', '-0.487', '-0.755', '-0.1976', '-0.01158', '-0.2406', '0.2708', '0.2683', '-0.853', '0.5854', '0.722', '-0.277', '-0.3523', '0.414', '-0.144', '0.645', '0.07117', '0.6567', '0.0527', '-0.5674', '0.8896', '0.0812']",,,,,,,
mondo:0009183,junctional epidermolysis bullosa with pyloric atresia,"['junctional epidermolysis bullosa - pyloric atresia', 'epidermolysis bullosa, junctional, with pyloric atresia', 'junctional epidermolysis bullosa-pyloric atresia syndrome', 'junctional epidermolysis bullosa with pyloric atresia', 'JEB-PA', 'epidermolysis bullosa, junctional, with pyloric atresia and aplasia cutis congenita', 'aplasia cutis congenita with gastrointestinal atresia', 'EB-Pa-ACC', 'epidermolysis bullosa JUNCTIONALIS with pyloric atresia', 'epidermolysis bullosa junctionalis with pyloric atresia', 'epidermolysis bullosa with pyloric atresia', 'epidermolysis bullosa, junctional, with pyloric stenosis', 'JEB-Pa', 'Carmi syndrome']",0060733,226730,79403,C1856934,"['0.631', '-0.014786', '-0.4792', '-0.2423', '0.1749', '-0.4001', '-0.587', '0.529', '-0.1499', '-0.7935', '0.2133', '-0.6616', '-1.142', '0.335', '-0.6772', '0.1475', '0.00478', '-0.974', '-0.246', '-0.7993', '-0.576', '-0.1044', '0.0809', '0.702', '0.2223', '0.2135', '-1.23', '0.6587', '-0.2942', '-0.801', '0.1635', '-0.2405', '-0.3865', '0.006393', '0.2434', '-0.0896', '-1.244', '0.2964', '1.13', '-0.268', '0.1175', '-0.5566', '0.04797', '0.00798', '0.1503', '-0.003853', '-0.408', '0.16', '0.2314', '-0.1797', '-0.874', '-1.025', '0.4678', '-0.2698', '-0.1676', '-0.4385', '-0.269', '1.171', '-0.7505', '-0.3384', '-0.0377', '0.6343', '-0.08936', '0.2952', '0.976', '0.4602', '0.1696', '-0.00849', '-0.7456', '0.2708', '-0.07245', '0.222', '-0.4404', '-0.38', '0.1891', '-0.1759', '0.1133', '-0.1414', '-0.3027', '-0.3337', '-0.904', '0.1487', '-0.2124', '-0.3396', '0.2191', '0.4932', '-0.722', '0.6895', '0.7935', '-0.12006', '-0.5464', '0.2366', '-0.3428', '0.6084', '0.2206', '0.7876', '0.3647', '-0.3687', '0.675', '0.1268']",,,C535377,,,,
mondo:0009184,epidermolysis bullosa with diaphragmatic hernia,['epidermolysis bullosa with diaphragmatic hernia'],,226735,,,,,,C565588,,,,
mondo:0009185,amelocerebrohypohidrotic syndrome,"['Kohlschutter Tonz syndrome', 'KOHLSCHUTTER-Tonz syndrome', 'Kohlschutter syndrome', 'epilepsy-dementia-amelogenesis imperfecta syndrome', 'Kohlschutter-Tonz syndrome', 'KTZS', 'epilepsy, dementia, and amelogenesis imperfecta', 'epilepsy dementia amelogenesis imperfecta', 'epilepsy and Yellow teeth']",0111668,226750,1946,C0406740,"['0.1378', '0.353', '0.3333', '-0.3342', '0.04462', '-0.67', '0.1515', '0.2651', '-0.1582', '-0.2445', '-0.5933', '-0.2075', '0.01436', '-0.49', '0.431', '-0.1471', '0.2083', '-0.1844', '0.004227', '-0.492', '0.1613', '0.0856', '-0.02522', '-0.1765', '0.1425', '0.00813', '-0.1305', '-0.3186', '-0.006863', '-0.11536', '0.03558', '0.1769', '0.3271', '0.3494', '0.1289', '-0.01985', '-0.2218', '-0.4438', '-0.5723', '-0.4463', '0.1433', '-0.5205', '0.221', '-0.0719', '-0.166', '-0.4978', '-0.161', '0.2593', '-0.0895', '0.2776', '0.252', '0.389', '0.002735', '-0.256', '0.1938', '-0.4768', '0.138', '-0.2593', '-0.2837', '0.32', '0.251', '-0.0758', '0.4504', '-0.1993', '-0.04547', '-0.0815', '0.2456', '0.1289', '-0.3843', '0.174', '-0.2089', '-0.05188', '0.01297', '0.05502', '0.1559', '0.1577', '0.238', '0.0275', '-0.536', '-0.10614', '0.1061', '0.4258', '-0.4485', '0.3826', '0.2617', '-0.01139', '0.1247', '0.469', '0.31', '0.04932', '0.3223', '0.5073', '0.005733', '0.1461', '0.305', '0.1964', '0.5645', '-0.287', '0.3704', '0.282']",,,C537213,,,,
mondo:0009186,"epilepsy, photogenic, with spastic diplegia and intellectual disability","['epilepsy, photogenic, with spastic diplegia and mental retardation', 'epilepsy, photogenic, with spastic diplegia and intellectual disability']",,226800,,C1856931,,,,C565587,,,,
mondo:0009187,celiac disease-epilepsy-cerebral calcification syndrome,"['bilateral occipital calcifications with epilepsy', 'epilepsy with bilateral occipital calcifications', 'celiac disease, epilepsy, and cerebral calcification syndrome', 'celiac disease epilepsy occipital calcifications', 'coeliac disease epilepsy occipital calcifications', 'coeliac disease, epilepsy, and cerebral calcification syndrome', 'epilepsy occipital calcifications', 'familial unilateral and bilateral occipital calcifications and epilepsy', 'CEC']",,226810,1459,C1856930,,,,C535496,,,,
mondo:0009188,epilepsy-telangiectasia syndrome,"['mental retardation, epilepsy, palpebral conjunctival telangiectasias and IgA deficiency', 'intellectual disability, epilepsy, palpebral conjunctival telangiectasias and IgA deficiency', 'epilepsy-telangiectasia', 'epilepsy telangiectasia']",,226850,1951,C1856929,,,,C535497,,,,
mondo:0009189,multiple epiphyseal dysplasia type 4,"['epiphyseal dysplasia, multiple, type 4', 'multiple epiphyseal dysplasia with double-layered patella', 'multiple epiphyseal dysplasia, autosomal recessive', 'MED4', 'autosomal recessive multiple epiphyseal dysplasia', 'epiphyseal dysplasia, multiple, 4', 'SLC26A2 multiple epiphyseal dysplasia (disease)', 'rMED', 'EDM4', 'multiple epiphyseal dysplasia with Bilayered patellae', 'multiple epiphyseal dysplasia with clubfoot', 'Polyepiphyseal dysplasia type 4', 'epiphyseal dysplasia multiple 4', 'multiple epiphyseal dysplasia 4']",0070300,226900,93307,C1847593,"['-0.239', '0.3752', '0.283', '-0.1604', '0.651', '-0.836', '-0.291', '0.829', '-0.7056', '-0.3494', '-0.163', '0.3376', '-0.00852', '0.0658', '0.01729', '0.3804', '0.365', '-0.07574', '-0.0475', '-0.4924', '-0.2769', '-0.28', '0.697', '-0.0128', '0.1598', '0.6416', '0.0432', '0.1681', '-0.1276', '-0.2103', '-0.2432', '-0.3875', '0.04007', '0.4556', '0.2507', '-0.707', '-0.09735', '-0.2751', '0.0377', '-0.1284', '-0.3403', '-0.4941', '-0.05624', '0.05325', '0.1981', '-0.4287', '-0.3027', '0.539', '0.00726', '-0.1377', '-0.01666', '-0.236', '-0.1118', '-0.04327', '-0.07654', '-0.9746', '-0.1991', '-0.296', '-0.2133', '-0.4692', '0.473', '-0.02034', '-0.3987', '0.1216', '-0.3142', '0.2468', '0.554', '0.361', '0.113', '-0.2764', '-0.181', '-0.3474', '0.16', '-0.395', '0.3516', '0.4106', '-0.3572', '0.4924', '-0.4724', '-0.1583', '-0.1884', '0.332', '-0.05383', '0.4734', '0.0703', '0.3662', '0.01836', '0.3445', '0.1466', '0.1107', '-0.2754', '0.2954', '0.2386', '0.1882', '0.5625', '0.4795', '0.321', '-0.1984', '0.2607', '0.0605']",,,C535504,,Q77.3,,
mondo:0009190,"epiphyseal dysplasia of femoral head, myopia, and deafness","['epiphyseal dysplasia of femoral head, myopia, and deafness']",,226950,,C1856918,,,,C565585,,,,
mondo:0009191,Lowry-Wood syndrome,"['Lowry-Wood syndrome', 'Lowry Wood syndrome', 'epiphyseal dysplasia, microcephaly, and NYSTAGMUS', 'LWS', 'epiphyseal dysplasia, microcephaly and nystagmus', 'epiphyseal dysplasia-microcephaly-nystagmus syndrome']",,226960,1824,C0796021,,,,C537038,,,10062600,
mondo:0009192,Wolcott-Rallison syndrome,"['epiphyseal dysplasia, multiple, with early-onset diabetes mellitus', 'Iddm-Med syndrome', 'WRS', 'Wolcott Rallison syndrome', 'epiphyseal dysplasia multiple with early-onset diabetes mellitus', 'Med-Iddm syndrome', 'Wolcott-Rallison syndrome', 'MED-IDDM syndrome', 'IDDM-MED syndrome', 'early-onset diabetes mellitus with multiple epiphyseal dysplasia']",0090060,226980,1667,C0432217,"['0.2269', '0.2837', '-0.2515', '0.1672', '0.2366', '0.003363', '0.6045', '0.6855', '-0.09753', '-0.4636', '-0.7554', '0.4758', '0.09467', '0.6885', '-0.5757', '0.1549', '0.381', '0.274', '-0.06323', '-1.088', '0.0676', '0.009995', '0.6157', '-0.4673', '-0.1337', '0.11456', '-0.07733', '0.4614', '0.0445', '-0.321', '0.3896', '-0.5254', '0.1039', '0.1619', '-0.18', '0.4194', '0.11456', '-0.7993', '-0.36', '0.466', '-0.1865', '-0.1426', '0.668', '-0.11005', '-0.1884', '-0.269', '0.3225', '-0.1942', '-0.2284', '0.00879', '0.1373', '0.5303', '0.411', '0.1514', '-0.1267', '-0.5415', '-0.3914', '-0.507', '0.3308', '-0.006035', '0.4763', '0.3123', '-0.2109', '-0.4', '-0.1132', '-0.16', '0.3784', '0.709', '0.0689', '-0.4', '0.0401', '-0.4402', '-0.1584', '-0.5117', '-0.01773', '0.1288', '0.497', '0.2537', '0.3474', '0.03653', '-0.2886', '0.156', '-0.515', '0.04495', '0.0358', '0.451', '-0.019', '0.04498', '0.5645', '-0.2896', '0.3223', '0.2433', '-0.008804', '0.014946', '0.435', '0.4814', '0.6187', '-0.3508', '-0.0785', '0.2397']",C131007,,C536739,,,,
mondo:0009193,"epithelial squamous dysplasia, keratinizing desquamative, of urinary tract","['epithelial squamous dysplasia, keratinizing desquamative, of urinary tract']",,226985,,C1856902,,,,C565584,,,,
mondo:0009194,immunodeficiency 32B,"['IMD32B', 'CAEBV syndrome', 'CAEBV infection', 'IRF8 deficiency, autosomal recessive', 'monocyte and dendritic cell deficiency, autosomal recessive', 'immunodeficiency 32B', 'chronic active Epstein-Barr virus infection', 'chronic EBV infection syndrome', 'CEBV', 'chronic Epstein-Barr virus infection syndrome', 'immunodeficiency 32B, monocyte, Dendritic cell, and natural Killer cell deficiency, autosomal recessive', 'Epstein-Barr VIRUS, susceptibility to chronic infection by', 'chronic active Epstein-Barr disease', 'immunodeficiency 32B, monocyte and dendritic cell deficiency, autosomal recessive']",0111985,614894,2566,,,,,,,,,
mondo:0009195,erythema of acral regions,['erythema of acral regions'],,227000,,,,,,,,,,
mondo:0009196,ermine phenotype,"['black locks with albinism and deafness syndrome', 'ermine phenotype', 'pigmentary disorder with hearing loss', 'BADS', 'BADS syndrome', 'O^Doherty syndrome']",,227010,999,C1856899,,,,C562663,270.2,E70.3,,
mondo:0009197,transient erythroblastopenia of childhood,"['familial transient erythroblastopenia of childhood', 'erythroblastopenia, transient', 'transient erythroblastopenia of childhood', 'tec', 'transient acquired pure red cell aplasia']",,227050,98871,C0451688,,C131683,,C536980,284.81,,,
mondo:0009198,congenital lethal erythroderma,"['congenital exfoliative erythroderma resistant to treatment', 'lethal congenital erythroderma', 'erythroderma, lethal congenital', 'erythroderma lethal congenital']",,227090,1954,,,,,C535513,,,,
mondo:0009199,ethanolaminosis,"['ethanolaminosis', 'ethanolamine kinase deficiency']",,227150,,C0268423,,,,C562651,270.8,,,
mondo:0009200,eyebrow duplication-syndactyly syndrome,"['eyebrows duplication of, with stretchable skin and syndactyly', 'eyebrows, DUPLICATION of, with stretchable skin and syndactyly']",,227210,3172,C1856896,,,,C536383,,,,
mondo:0009201,"facial abnormalities, kyphoscoliosis, and intellectual disability","['facial abnormalities, kyphoscoliosis, and mental retardation', 'facial abnormalities, kyphoscoliosis, and intellectual disability']",,227250,,C1856893,,,,C565580,,,,
mondo:0009202,Thakker-Donnai syndrome,"['facial dysmorphism with multiple malformations', 'dysmorphic facial features and multiple structural abnormalities', 'Dysmorphism multiple structural anomalies', 'Dysmorphism-multiple structural anomalies syndrome']",,227255,1780,C2931219,,,,C536503,,,,
mondo:0009203,focal facial dermal dysplasia type III,"['focal facial dermal dysplasia type 2', 'FFDD type 2', 'FFDD type III', 'Setleis syndrome', 'focal Facial dermal dysplasia, type II', 'focal Facial dermal dysplasia, type II, formerly', 'focal facial dermal dysplasia 3, Setleis type', 'facial ectodermal dysplasia', 'FFDD3', 'bitemporal forceps marks syndrome', 'bitemporal forceps Marks syndrome']",,227260,1807,,"['0.2289', '0.0795', '0.1351', '-0.6807', '-0.171', '0.5044', '0.4326', '0.82', '-0.307', '-0.5264', '0.131', '-0.1282', '0.2345', '-0.1484', '-0.4084', '0.652', '0.968', '-1.042', '-0.0705', '-0.749', '-0.1304', '0.4348', '0.7407', '0.547', '0.11017', '-0.423', '-0.1106', '0.2695', '0.502', '0.0702', '0.2957', '0.07666', '0.2198', '0.266', '0.0994', '0.02396', '-0.766', '-0.352', '-0.03354', '-0.5083', '-0.0527', '-0.3271', '-0.655', '-0.01761', '0.3137', '-0.489', '0.7305', '0.3604', '-0.2101', '-0.2235', '0.1473', '-0.02081', '-0.003778', '0.3044', '-0.576', '-0.2815', '0.1969', '-0.5674', '-0.4475', '0.2976', '-0.1561', '0.0743', '-0.468', '-0.127', '0.0709', '0.3936', '0.361', '0.08356', '-0.329', '0.5186', '-0.1523', '0.3035', '0.1002', '-0.1277', '-0.1026', '0.05124', '-0.207', '-0.5195', '-0.304', '-0.2642', '0.11664', '-0.1936', '0.5913', '0.6997', '0.1017', '-0.2146', '-0.1212', '0.75', '0.599', '0.802', '0.2634', '0.3457', '0.2776', '0.3706', '0.975', '0.0551', '-0.2588', '0.05194', '0.3735', '0.4304']",,,,,,,
mondo:0009204,lethal faciocardiomelic dysplasia,"['faciocardiomelic dysplasia lethal', 'faciocardiomelic dysplasia, lethal']",,227270,1972,C1856891,,,,C565578,,,,
mondo:0009205,faciocardiorenal syndrome,"['Eastman-Bixler syndrome', 'faciocardiorenal syndrome', 'Eastman Bixler syndrome']",,227280,1973,C0795936,,,,C536388,,,,
mondo:0009206,"factor V and factor VIII, combined deficiency of, type 1","['F5F8D1', 'multiple coagulation Factor deficiency 1', 'factor 5 and Factor VIII, combined deficiency of, 1', 'FMFD 1', 'familial multiple coagulation Factor deficiency 1', 'combined deficiency of factor V and factor VIII caused by mutation in LMAN1', 'combined factor V and VIII deficiency', 'LMAN1 combined deficiency of factor V and factor VIII', 'factor V and factor VIII, combined deficiency of, 1']",,227300,,,,,,,,,,
mondo:0009207,"factor V and factor VIII, combined deficiency of, with normal protein C and protein C inhibitor","['factor 5 and Factor VIII, combined deficiency Of, with normal Protein C and Protein C inhibitor', 'factor V and Factor VIII, combined deficiency of, with normal protein c and Protein C inhibitor']",,227310,,C1856882,,,,,,,,
mondo:0009208,faciothoracogenital syndrome,"['facio thoraco genital syndrome', 'faciothoracogenital syndrome', 'congenital anomalies, involving mainly the face, thorax, and genitalia']",,227320,,C2931184,,,,C536387,,,,
mondo:0009209,autosomal recessive faciodigitogenital syndrome,"['facio-digito-genital syndrome, Kuwait type', 'faciodigitogenital syndrome, autosomal recessive', 'Aarskog-like syndrome', 'Kuwait type faciodigitogenital syndrome', 'Teebi-Naguib-Alawadi syndrome']",,227330,1974,,,,,,,,,
mondo:0009210,congenital factor V deficiency,"['labile factor deficiency', 'Owren disease', 'hereditary hypoproaccelerinaemia', 'labile Factor deficiency', 'Parahemophilia', 'hereditary factor V deficiency', 'Owren Parahemophilia', 'deficiency, labile', 'hereditary Factor V deficiency', 'Proaccelerin deficiency', 'factor V deficiency', 'factor 5 deficiency']",2216,227400,326,C0015499,"['-0.1448', '-0.0664', '-0.819', '-0.3333', '0.1812', '0.009514', '-0.0894', '0.536', '-0.4077', '0.02391', '0.00748', '0.4595', '0.1755', '0.3003', '0.1658', '-0.153', '0.0741', '0.1987', '-0.3694', '-0.79', '-0.3577', '-0.1986', '0.746', '-0.01971', '0.1035', '-0.1181', '0.1729', '0.471', '0.365', '0.03558', '0.4463', '-0.1934', '0.5547', '0.5195', '-0.4268', '-0.3274', '-0.1976', '-0.3662', '0.0781', '-0.01094', '-0.1416', '-0.02983', '0.435', '-0.1348', '0.3547', '-0.05795', '0.04675', '0.0834', '0.4604', '0.3472', '0.5522', '-0.8667', '0.1802', '-0.114', '-0.3853', '0.238', '-0.2281', '0.2196', '-0.4893', '0.2189', '-0.4065', '-0.0687', '0.1975', '-0.0662', '0.2854', '0.404', '0.1853', '-0.002172', '-0.2449', '-0.0706', '-0.611', '-0.3855', '-0.4324', '-0.7144', '0.8364', '-0.1115', '1.067', '-0.0605', '0.3474', '-0.2151', '-0.761', '-0.256', '-0.07404', '0.283', '0.222', '0.2766', '0.1864', '0.1912', '0.4292', '-0.6865', '0.2808', '0.7246', '0.2776', '-0.1523', '0.695', '0.688', '0.3523', '-0.569', '0.03117', '-0.1478']",C98938,,,,,10048930,
mondo:0009211,congenital factor VII deficiency,"['factor VII deficiency', 'hypoproconvertinemia', 'congenital proconvertin deficiency', 'factor 7 deficiency', 'F7 deficiency']",2215,227500,327,C1394919,"['-0.3374', '-0.1456', '-0.9883', '0.3013', '-0.511', '0.1375', '0.05673', '0.363', '-0.328', '0.2483', '0.01378', '0.1284', '0.2883', '-0.298', '0.1436', '-0.0749', '0.1236', '-0.002487', '-0.0687', '-0.815', '-0.4138', '-0.177', '0.767', '-0.1277', '0.178', '0.3215', '0.2203', '0.2446', '0.2158', '-0.1015', '0.5376', '-0.2917', '-0.09454', '0.728', '-0.72', '-0.4138', '-0.02818', '-0.226', '0.083', '-0.3457', '0.2036', '-0.2734', '0.2179', '-0.4148', '0.514', '-0.02359', '0.1719', '-0.2664', '0.3752', '0.7593', '0.1318', '-0.6665', '0.159', '0.168', '-0.02583', '0.6455', '0.2605', '-0.662', '-0.3', '0.164', '-0.3179', '-0.00429', '0.641', '-0.2886', '0.4126', '0.02026', '0.835', '-0.1797', '-0.6963', '0.05255', '-0.1266', '-0.554', '0.0013485', '-0.04095', '0.5386', '0.1792', '0.8184', '-0.1593', '0.3176', '-0.636', '-0.367', '-0.06635', '-0.1644', '0.5283', '0.0426', '0.08734', '-0.1371', '0.703', '0.4377', '-0.563', '0.12445', '0.915', '-0.2015', '0.11346', '0.645', '0.3625', '0.04642', '-0.827', '-0.1469', '-0.2235']",C131631,,,,,10016079,
mondo:0009212,congenital factor X deficiency,"['F10 deficiency', 'Stuart-Prower factor deficiency', 'hereditary Factor X deficiency', 'factor X deficiency, congenital', 'factor X deficiency', 'Stuart factor deficiency, congenital', 'Stuart-Prower Factor deficiency', 'factor 10 deficiency', 'disease, Stuart-Prower', 'congenital Stuart factor deficiency']",2222,227600,328,,"['-0.343', '-0.1698', '-0.6187', '-0.7407', '-0.0636', '0.08167', '0.1837', '0.609', '-0.01855', '0.0162', '-0.1389', '0.1251', '0.586', '0.2484', '-0.0175', '0.1765', '0.1129', '0.1492', '-0.345', '-0.5444', '-0.3926', '-0.1621', '0.9805', '-0.0889', '0.05908', '-0.0726', '0.4146', '0.1364', '0.3025', '0.08405', '0.02101', '0.1777', '0.5815', '0.5312', '-0.8203', '-0.218', '-0.01251', '-0.5283', '0.1516', '-0.0003843', '0.43', '-0.4905', '0.107', '0.06445', '0.5396', '0.3145', '-0.1985', '0.1056', '0.5215', '0.534', '0.6465', '-0.742', '0.03008', '-0.217', '-0.223', '0.3284', '0.2952', '0.04617', '-0.45', '-0.11884', '-0.1971', '-0.4937', '0.318', '-0.05325', '0.2002', '0.269', '0.471', '0.05307', '-0.1909', '0.1387', '-0.4766', '-0.4563', '-0.573', '-0.8613', '0.899', '0.06366', '0.9604', '0.0599', '0.2026', '-0.0968', '-0.4958', '0.1956', '0.5083', '0.2037', '-0.04266', '-0.008804', '0.3809', '0.4', '0.0908', '-0.4287', '0.0816', '1.266', '0.5444', '0.1548', '0.5713', '0.2979', '0.2942', '-0.9917', '0.3306', '0.1602']",C98940,,,286.3,,,
mondo:0009213,Fanconi anemia complementation group C,"['Fanconi anemia, complementation group C', 'Fanconi Anemia, complementation group type C', 'Fanconi pancytopenia, type 3', 'FA3', 'FANCC', 'Fanconi anemia complementation group type C', 'Fanconi pancytopenia type 3', 'Fanconi anaemia complementation group type C', 'FACC', 'facc']",0111087,227645,,C3468041,,C125704,,,,,,
mondo:0009214,Fanconi anemia complementation group D2,"['FANCD2', 'FA4', 'Fanconi anemia, complementation group D2', 'FAD2', 'Fanconi pancytopenia, type 4', 'Fad2', 'Fanconi pancytopenia type 4', 'Fanconi Anemia, complementation group D']",0111083,227646,,C3160738,,C125706,,,,,,
mondo:0009215,Fanconi anemia complementation group A,"['Estren-Dameshek variant of Fanconi Anemia', 'Fanconi anaemia caused by mutation in FANCA', 'Fanconi anemia caused by mutation in FANCA', 'Fanconi Anemia', 'FANCA', 'Fanconi anemia, complementation group A', 'Estren-Dameshek variant of Fanconi pancytopenia', 'Fanconi Anemia, complementation group type a', 'FANCA Fanconi anemia', 'Fanconi anaemia complementation group type A', 'Estren-Dameshek variant of Fanconi Anaemia', 'Fanconi Anemia, Estren-Dameshek variant', 'FANCA Fanconi anaemia', 'Fanconi anemia complementation group type A', 'Fanconi Anaemia']",0111095,227650,,CN653908,"['-0.3357', '0.2634', '0.00644', '0.403', '0.663', '0.1103', '-0.3757', '0.413', '-0.2922', '-0.57', '0.791', '-0.02931', '0.2092', '0.6245', '-1.073', '0.1719', '-0.487', '0.344', '-0.527', '-0.3223', '-0.2827', '-0.551', '0.318', '-0.247', '0.93', '-0.533', '0.0732', '-0.3252', '0.571', '0.0481', '0.2025', '0.2407', '0.3403', '0.4387', '0.6606', '-0.343', '-0.8003', '-0.4724', '0.4207', '-0.2722', '-0.737', '0.09845', '0.2025', '-0.4236', '-0.673', '-0.908', '0.2493', '0.05914', '0.6494', '-0.1832', '0.501', '0.1847', '0.7173', '-0.2556', '0.3647', '-0.8135', '0.2479', '0.635', '-1.003', '-0.04895', '-0.09216', '0.304', '-0.4285', '-0.3096', '0.09357', '0.2411', '0.318', '0.8887', '-0.535', '1.038', '0.867', '-0.2866', '-0.4917', '-0.591', '0.3516', '0.9536', '0.1882', '0.3557', '-0.0386', '0.261', '0.2583', '-0.2', '0.0639', '0.07275', '0.399', '-0.424', '-0.651', '0.4604', '0.965', '-0.1561', '0.501', '0.2656', '-0.333', '-0.12067', '0.567', '1.097', '0.2067', '-0.1613', '0.1647', '-0.6357']",C125702,0009044,,,,,
mondo:0009216,glycogen storage disease due to GLUT2 deficiency,"['glycogenosis Fanconi EXACT', 'glycogen storage disease 11', 'GSD due to GLUT2 deficiency', 'Fanconi Bickel syndrome', 'hepatic glycogenosis with Fanconi nephropathy', 'Fanconi syndrome with intestinal malabsorption and galactose intolerance', 'Fanconi-Bickel disease', 'hepatorenal glycogenosis with renal fanconi syndrome', 'Fanconi-Bickel syndrome', 'glycogen storage disease type 11', 'glycogen storage disease type XI', 'GSD type 11', 'GLUT2 deficiency', 'FBS', 'glycogen storage disease XI', 'glycogen storage disease due to GLUT2 deficiency', 'pseudo-phlorizin diabetes', 'Bickel-Fanconi glycogenosis', 'hepatic glycogenosis with amino aciduria and glucosuria', 'GSD type XI', 'glycogenosis, Fanconi type', 'hepatorenal glycogenosis with renal Fanconi syndrome', 'glycogenosis due to GLUT2 deficiency']",,227810,2088,,"['-0.2998', '-0.01996', '0.0289', '0.406', '0.09344', '-0.839', '-0.6436', '1.236', '-0.1898', '0.0705', '0.04053', '0.1642', '0.01811', '0.21', '-0.1808', '-0.221', '0.2812', '0.3582', '-0.2228', '-0.3054', '0.5923', '-0.727', '0.6187', '-0.09454', '-0.1956', '-0.2544', '0.05698', '-0.03287', '-0.315', '-0.02339', '0.4998', '-0.6636', '-0.1971', '0.00578', '-0.619', '-0.2864', '-0.1943', '0.084', '-0.00934', '0.2417', '-0.3345', '-0.09784', '0.4773', '0.5044', '-0.4692', '-0.6514', '0.0002111', '-0.3708', '-0.625', '0.3704', '-0.1534', '-0.2107', '0.531', '0.02173', '0.1051', '-0.7446', '0.6333', '-0.2986', '-0.7827', '0.3213', '0.3433', '0.2253', '0.1142', '-0.5273', '0.1952', '-0.09', '0.2817', '0.2015', '-0.5405', '-0.3264', '-0.55', '-0.4846', '0.197', '-0.0311', '0.1582', '-0.02087', '-0.1324', '0.01907', '-0.4963', '0.499', '0.1948', '-0.0593', '0.1909', '0.0783', '0.002254', '0.624', '0.214', '0.10706', '0.979', '0.3396', '0.662', '0.5723', '-0.513', '-0.0897', '0.1753', '0.291', '0.4182', '-0.5464', '0.292', '0.009544']",,,,,,,
mondo:0009217,Fanconi-like syndrome,['Fanconi-like syndrome'],0090066,227850,,C0151638,,,,C536855,,,,
mondo:0009218,Farber lipogranulomatosis,"['FRBRL', 'N-Laurylsphingosine deacylase deficiency', 'N-LAURYLSPHINGOSINE deacylase deficiency', 'AC deficiency', 'Farber^s disease', 'Farber disease', 'ceramidase deficiency', 'acid ceramidase deficiency', 'Farber lipogranulomatosis']",0050464,228000,333,CN204335,"['-0.1858', '-0.2568', '-0.0757', '-0.08014', '0.1735', '-0.755', '-0.2744', '0.2563', '-0.3018', '-0.3005', '-0.4185', '-0.2042', '-0.596', '-0.001027', '0.04663', '-0.2156', '0.003582', '-0.3374', '0.0641', '-0.825', '-0.1649', '-0.46', '0.796', '-0.404', '-0.651', '-0.416', '0.2896', '0.1733', '-0.2705', '-0.2744', '0.4888', '0.256', '0.4558', '0.1484', '0.1823', '-0.4893', '-0.7256', '0.3184', '0.7524', '0.004223', '-0.06476', '-0.864', '0.2078', '0.1443', '0.3503', '0.09564', '-0.2866', '-0.149', '-0.0637', '0.02661', '-0.1483', '0.4956', '0.4116', '0.625', '0.382', '-0.1953', '0.3066', '0.473', '0.3213', '-0.05585', '-0.06204', '-0.2218', '-0.3508', '-0.273', '-0.12134', '-0.2544', '0.1925', '0.6377', '-0.358', '0.2874', '-0.4521', '-0.5635', '-0.1672', '0.3728', '0.4014', '-0.01875', '0.6055', '-0.4255', '-0.5415', '-0.3', '-0.4963', '-0.1478', '-0.2336', '0.1896', '0.1284', '0.65', '-0.2808', '0.4124', '0.2954', '-0.0925', '0.4448', '0.0147', '-0.1964', '0.0726', '0.3552', '0.3135', '0.6763', '0.05292', '0.8', '-0.000751']",C84710,,D055577,272.8,,,
mondo:0009219,"fascial dystrophy, congenital","['fascial dystrophy, congenital']",,228020,,,,,,C563219,709.8,,,
mondo:0009220,"visceral steatosis, congenital","['visceral steatosis, congenital', 'fatty liver disease, congenital', 'White liver disease', 'fatal neonatal hepatic steatosis', 'fatty metamorphosis of viscera', 'visceral steatosis', 'steatosis of liver']",,228100,,,,,,C536351,571.8,,,
mondo:0009221,femur-fibula-ulna complex,"['FFU complex', 'femur fibula ulna syndrome', 'femur-fibula-ulna dysostosis', 'PFFD', 'femur-fibula-ulna syndrome', 'Ffu syndrome']",,228200,2019,C1856790,,,,C537918,,,10068448,
mondo:0009222,Gollop-Wolfgang complex,"['Gollop-Wolfgang complex', 'bifid femur-monodactylous ectrodactyly syndrome', 'femur bifid with monodactylous ectrodactyly', 'GWC', 'femur, unilateral bifid, with monodactylous ectrodactyly']",,228250,1986,C1856789,,,,C537917,,,,
mondo:0009223,hypogonadotropic hypogonadism 23 with or without anosmia,"['LHB hypogonadotropic hypogonadism', 'fertile eunuch syndrome', 'Pasqualini syndrome', '46,XY disorder of sex development due to LHB deficiency', 'Leydig cell hypoplasia due to LHB deficiency', 'eunuchoidism with spermatogenesis, normal FSH and low or normal interstitial cell-stimulating hormone (ICSH)', 'HH23', 'hypogonadotropic hypogonadism caused by mutation in LHB', '46,XY DSD due to luteinizing hormone subunit beta deficiency', 'Leydig cell hypoplasia due to luteinizing hormone subunit beta deficiency', '46,XY disorder of sex development due to luteinizing hormone subunit beta deficiency', '46,XY DSD due to LHB deficiency', 'hypogonadotropic hypogonadism 23 without anosmia']",0090091,228300,325448,C0271582,"['-0.369', '0.1382', '0.1063', '0.0208', '0.0909', '-0.2058', '-0.05063', '0.1757', '-0.2173', '-0.2218', '0.0587', '-0.07007', '-0.1355', '-0.02559', '0.03293', '-0.1664', '0.000578', '-0.03372', '-0.1688', '-0.29', '0.03293', '-0.1589', '0.1539', '-0.0455', '0.1775', '0.02167', '0.004982', '0.0228', '0.001278', '-0.139', '0.1274', '0.09814', '0.2646', '0.01985', '0.08575', '-0.1527', '0.02428', '-0.11804', '-0.00846', '-0.1925', '0.1416', '-0.09314', '0.07947', '0.0151', '-0.1131', '-0.2366', '0.12335', '-0.03644', '0.05295', '-0.005432', '0.08954', '-0.1113', '0.0741', '0.0699', '-0.1595', '-0.0684', '0.3025', '-0.01707', '-0.274', '0.1451', '0.0168', '0.1445', '0.1338', '0.03342', '0.1024', '0.1605', '0.1445', '0.1465', '-0.172', '0.1459', '-0.1917', '0.00968', '0.1001', '-0.1505', '0.1476', '-0.0788', '0.05463', '-0.0352', '-0.1211', '0.03137', '-0.06216', '0.04425', '-0.04477', '0.0872', '0.00533', '-0.2118', '0.1473', '0.2135', '0.3372', '0.0885', '0.0526', '0.1058', '-0.002762', '-0.2286', '0.4578', '0.1495', '0.133', '-0.2947', '0.02812', '0.0647']",,,C537919,253.4,,,
mondo:0009224,fetal iodine syndrome,"['fetal iodine deficiency disorder', 'foetal iodine deficiency disorder', 'endemic cretinism', 'FIDD']",,228355,1910,C4273860,,,,,,,,
mondo:0009225,"fever, familial lifelong persistent","['fever, familial lifelong persistent']",,228400,,C1856788,,,,C565569,,,,
mondo:0009226,fibrochondrogenesis 1,"['fibrochondrogenesis 1', 'FBCG1', 'fibrochondrogenesis caused by mutation in COL11A1', 'fibrochondrogenesis type 1', 'COL11A1 fibrochondrogenesis']",0080672,228520,,C3278138,,,,,,,,
mondo:0009227,"myofibromatosis, infantile, 1","['myofibromatosis caused by mutation in PDGFRB', 'IMF1', 'myofibromatosis, infantile, 1', 'myofibromatosis, infantile, type 1', 'fibromatosis, congenital generalised', 'myofibromatosis, juvenile', 'fibromatosis, congenital generalized', 'PDGFRB myofibromatosis']",,228550,,,,,,C562978,756.9,,,
mondo:0009228,gingival fibromatosis-facial dysmorphism syndrome,"['fibromatosis, gingival, with distinctive facies', 'gingival fibromatosis with distinctive facies', 'gingival fibromatosis with craniofacial dysmorphism']",,228560,2025,C1856761,,,,C565567,,,,
mondo:0009229,hyaline fibromatosis syndrome,"['hyalinosis, systemic', 'inherited systemic hyalinosis', 'juvenile hyaline fibromatosis (former subtype)', 'hyaline fibromatosis syndrome', 'HFS', 'infantile systemic hyalinosis (former subtype)']",0111669,228600,498474,C2745948,"['-0.0873', '0.0916', '0.04962', '-0.01877', '0.04095', '-0.0982', '-0.00875', '0.04932', '-0.0707', '-0.02576', '-0.02388', '0.03674', '0.00996', '-0.02016', '-0.02942', '-0.006874', '0.02519', '-0.04788', '-0.02295', '-0.1361', '0.00866', '-0.02068', '0.07635', '-0.03955', '0.02515', '0.015175', '-0.02565', '-0.02289', '0.01749', '-0.05258', '0.04053', '0.004757', '0.0565', '0.03586', '0.04272', '-0.008705', '-0.02196', '-0.0252', '-0.01677', '-0.1071', '0.01846', '-0.109', '0.00825', '-0.02214', '0.009', '-0.0802', '-0.03033', '0.0767', '0.02269', '0.0172', '-0.02518', '0.00441', '0.02715', '0.04358', '-0.0809', '-0.086', '0.07', '-0.02634', '-0.104', '0.003765', '0.0665', '0.02417', '-0.03305', '0.00971', '0.0053', '-0.02356', '0.1142', '0.04187', '-0.04938', '0.0905', '-0.0815', '-0.01848', '0.02878', '-0.02614', '-0.008835', '0.02077', '0.001634', '0.03564', '-0.0703', '-0.05878', '0.00836', '-0.00901', '-0.01427', '0.0806', '-0.0186', '-0.02243', '0.00863', '0.101', '0.0431', '-0.002487', '0.06104', '0.0981', '0.0309', '0.04785', '0.1359', '-0.01536', '0.0882', '-0.119', '0.02612', '0.0501']",,,,,,,
mondo:0009230,"fibrosclerosis, multifocal","['multifocal fibrosclerosis', 'mediastinal fibrosis, familial', 'fibrosclerosis, multifocal', 'retroperitoneal fibrosis, familial']",,228800,,,,,,C537375,710.8,M35.5,,
mondo:0009231,acromesomelic dysplasia 2B,"['fibular hypoplasia and complex brachydactyly', 'Du Pan syndrome', 'fibular aplasia-complex brachydactyly syndrome', 'acromesomelic dysplasia 2B']",0050790,228900,2639,C1856738,"['-0.3467', '0.1438', '0.006176', '-0.09875', '0.2412', '-0.3342', '-0.1003', '0.2012', '-0.1375', '-0.602', '-0.1497', '-0.04605', '-0.099', '-0.3015', '0.0788', '0.03735', '0.3037', '-0.00742', '-0.284', '-0.2842', '-0.0403', '-0.03452', '0.09625', '-0.1121', '0.2905', '0.1915', '-0.07416', '-0.08655', '0.4243', '-0.1066', '0.1643', '0.0413', '0.1415', '0.0894', '0.3237', '-0.429', '0.1121', '-0.4688', '0.1278', '-0.2844', '-0.1086', '-0.613', '0.05777', '-0.1459', '-0.03146', '-0.4224', '-0.2202', '0.3362', '0.2786', '-0.1328', '0.10236', '-0.2188', '-0.181', '0.2365', '-0.3396', '-0.4224', '0.4695', '-0.054', '-0.4407', '0.1641', '0.0369', '0.274', '0.253', '-0.02425', '-0.06354', '-0.1014', '-0.0391', '0.212', '-0.4856', '-0.1428', '-0.431', '0.0837', '0.02522', '0.07275', '0.4644', '0.402', '0.05038', '0.09576', '-0.1953', '0.02658', '0.1615', '0.2494', '0.4365', '0.2961', '0.0838', '0.1266', '0.1544', '0.734', '0.03137', '0.05173', '-0.1372', '0.4211', '-0.003008', '-0.08014', '0.7124', '0.1', '0.612', '-0.886', '0.01551', '-0.000567']",,,C537931,,,,
mondo:0009232,Fuhrmann syndrome,"['fibular hypoplasia or aplasia-femoral bowing-oligodactyly syndrome', 'fibular aplasia or hypoplasia, femoral bowing and poly-, syn-, and oligodactyly', 'Fuhrmann syndrome', 'bowing of the femurs, aplasia or hypoplasia of the fibula, and digital anomalies', 'Fuhrmann-Rieger-de Sousa syndrome']",0090067,228930,2854,C1856728,"['-0.4004', '-0.3657', '0.1012', '-0.1865', '0.3408', '-0.5337', '-0.294', '0.8486', '-0.3357', '-0.614', '-0.4875', '-0.4966', '-0.4255', '0.0721', '-0.1747', '-0.022', '0.674', '-0.2793', '-0.1947', '-0.6353', '-0.1685', '-0.1277', '0.4402', '-0.319', '0.5317', '0.10986', '-0.1329', '0.0507', '0.1903', '-0.546', '0.652', '-0.507', '-0.02219', '0.2766', '0.511', '-0.2717', '0.2502', '-0.692', '0.2603', '-0.1521', '-0.1284', '-0.3513', '0.1543', '-0.1771', '0.11664', '-0.5874', '-0.1531', '0.189', '-0.2303', '0.04028', '-0.0218', '-0.4607', '0.57', '0.3467', '-0.941', '-0.839', '-0.2225', '0.06616', '-0.339', '0.1035', '0.10614', '-0.2927', '-0.04163', '-0.01088', '-0.395', '0.02486', '-0.2747', '0.0882', '-0.917', '0.2413', '0.0882', '-0.217', '-0.0797', '-0.1791', '-0.0877', '0.1637', '-0.3855', '0.04306', '-0.2659', '0.2627', '-0.2988', '0.4548', '0.462', '0.4028', '-0.0631', '-0.2019', '-0.552', '0.498', '-0.0662', '-0.4106', '-0.5093', '0.434', '0.2507', '-0.07245', '0.7715', '0.0624', '0.648', '-1.073', '0.6094', '-0.3962']",,,C538189,,,,
mondo:0009233,Fibulo-ulnar hypoplasia-renal anomalies syndrome,"['FIBULOULNAR aplasia or hypoplasia with renal abnormalities', 'Saito Kuba Tsuruta syndrome', 'Fibulo ulnar hypoplasia renal anomalies', 'Saito-Kuba-Tsuruta syndrome']",,228940,2256,C1856727,,,,C537226,,,,
mondo:0009234,congenital high-molecular-weight kininogen deficiency,"['Flaujeac factor deficiency', 'Fitzgerald trait', 'Flaujeac trait', 'kininogen deficiency, total', 'HMWK', 'HMWK deficiency', 'Flaujeac trait, included', 'kininogen deficiency', 'Williams trait', 'Williams trait, included', 'kininogen deficiency, high molecular weight and Low molecular weight', 'high-molecular-weight kininogen deficiency, congenital', 'kininogen deficiency, high molecular weight', 'kininogen deficiency, high molecular weight and LOW molecular weight, included', 'Fitzgerald trait kininogen deficiency, total, included', 'high molecular weight kininogen deficiency']",0111676,228960,483,,"['-0.4805', '0.04468', '-0.0676', '0.1237', '-0.2046', '0.12067', '-0.2605', '0.02043', '0.1462', '-0.0764', '0.00959', '0.1179', '0.2416', '-0.0576', '0.02573', '-0.1472', '0.1844', '0.02544', '-0.1603', '-0.704', '0.1157', '0.03427', '0.5317', '-0.06476', '0.02022', '0.08466', '0.1738', '-0.06757', '-0.1844', '0.008995', '0.4175', '0.07153', '0.2454', '0.483', '-0.2162', '-0.15', '0.02756', '-0.09894', '0.08923', '-0.3623', '0.1465', '-0.0985', '0.0951', '-0.1827', '-0.3025', '-0.37', '-0.2164', '-0.1154', '0.3816', '0.3774', '0.1561', '-0.1051', '0.2083', '0.1313', '-0.461', '-0.02274', '0.159', '-0.005844', '-0.7017', '0.1774', '-0.0254', '0.1484', '0.3098', '-0.2296', '0.0831', '0.08295', '0.21', '-0.04715', '-0.1755', '0.337', '-0.0665', '-0.1448', '-0.2448', '-0.1736', '0.5146', '0.07825', '0.4424', '-0.05615', '0.2134', '-0.12384', '-0.3672', '-0.2313', '0.2688', '0.1492', '-0.1051', '0.212', '0.2064', '0.43', '0.419', '0.02617', '0.2546', '0.5376', '-0.1921', '-0.1346', '0.4446', '0.448', '0.04913', '-0.379', '-0.2375', '0.4316']",C98946,,C537060,286.9,,,
mondo:0009235,familial benign flecked retina,"['FRFB', 'fleck retina, familial benign', 'FLECK retina, familial benign']",0111677,228980,363989,C1856718,"['-0.426', '0.1183', '0.02158', '0.07776', '0.169', '-0.1888', '-0.00855', '0.10925', '-0.2042', '0.04913', '-0.19', '-0.2397', '-0.2751', '-0.1729', '-0.03217', '-0.09814', '0.1847', '-0.122', '0.2466', '-0.4915', '-0.2683', '-0.06168', '0.2375', '0.2096', '-0.134', '0.2418', '-0.02817', '-0.155', '-0.097', '0.264', '0.4778', '-0.02808', '0.0628', '0.1576', '-0.0833', '0.05737', '0.11993', '-0.1091', '0.015076', '-0.3826', '0.3367', '-0.4958', '0.06216', '-0.1349', '-0.0945', '0.1877', '-0.1448', '-0.07184', '0.0986', '0.002115', '0.3665', '0.0848', '0.06604', '-0.01968', '-0.08514', '-0.2798', '0.594', '-0.1724', '-0.4954', '0.01608', '0.2395', '-0.05872', '0.1484', '0.141', '0.01784', '0.02936', '0.515', '0.523', '-0.2568', '0.3306', '-0.1676', '-0.2137', '0.2057', '0.09985', '0.268', '0.0398', '0.05826', '0.11505', '-0.04126', '-0.4102', '-0.02397', '0.2125', '-0.0002162', '0.3665', '-0.12177', '-0.3281', '0.12213', '0.2081', '0.2734', '0.0768', '0.2864', '0.405', '0.1968', '0.06195', '0.5327', '-0.1692', '0.3564', '-0.3086', '4.85e-05', '0.2612']",,,C565564,,H35.5,,
mondo:0009236,Kandori fleck retina,['FLECK retina of KANDORI'],,228990,99179,C0271257,,,,C562701,,H35.5,,
mondo:0009237,focal epithelial hyperplasia,"['heck^s disease', 'focal epithelial hyperplasia, oral', 'FEH, oral', 'heck disease', 'multifocal epithelial hyperplasia']",5362,229045,,C0206067,,C97083,0007275,D017573,528.79,,,
mondo:0009238,hereditary folate malabsorption,"['folic acid transport defect', 'congenital defect of folate absorption', 'folate malabsorption, hereditary', 'congenital folate malabsorption']",0111678,229050,90045,C0342705,"['0.1652', '0.1482', '0.02255', '-0.269', '-0.2052', '-0.05975', '-0.5586', '0.5957', '-0.4287', '0.05417', '-0.1982', '-0.11847', '0.1735', '0.2294', '-0.1383', '-0.05884', '-0.00858', '-0.12024', '-0.5596', '-1.032', '0.2812', '-0.1328', '0.2515', '0.3875', '-0.0551', '-0.11096', '-0.2732', '0.4028', '-0.2002', '-0.56', '0.3464', '0.1042', '0.1709', '0.466', '-0.1722', '0.2439', '-0.614', '-0.2637', '-0.4004', '0.534', '0.00948', '-0.11694', '0.5747', '-0.2179', '-0.6914', '-0.3645', '0.1366', '-0.3665', '-0.11316', '-0.1305', '0.1838', '0.2272', '0.2578', '0.1709', '0.2659', '0.728', '0.248', '-0.009155', '-0.8047', '0.517', '-0.01247', '0.3313', '0.6807', '-0.2163', '0.39', '-0.08966', '0.6475', '0.272', '-0.4421', '0.452', '0.1353', '-0.132', '-0.7227', '-0.1114', '0.07825', '0.1836', '0.678', '-0.1848', '0.4072', '0.1531', '0.06186', '0.01657', '0.06396', '0.2345', '0.506', '0.0744', '-0.2328', '-0.2157', '0.3008', '0.0894', '0.32', '0.0864', '-0.01685', '-0.3333', '0.3484', '1.034', '0.2206', '-0.421', '0.241', '0.1439']",C156424,,C562799,,,,
mondo:0009239,hypogonadotropic hypogonadism 24 without anosmia,"['HH24', 'hypogonadotropic hypogonadism caused by mutation in FSHB', 'hypogonadotropic hypogonadism 24 without anosmia', 'FSHB hypogonadotropic hypogonadism', 'isolated follicle-stimulating hormone deficiency', 'isolated follicle stimulating hormone deficiency', 'follicle-stimulating hormone deficiency, isolated', 'isolated follicle-stimulating hormone (FSH) deficiency', 'isolated FSH deficiency']",0090088,229070,52901,C1856716,"['-0.806', '0.10547', '0.1782', '-0.2593', '0.2108', '0.04935', '-0.04852', '0.1252', '-0.3347', '-0.2742', '0.1235', '0.2502', '-0.0378', '0.1724', '0.2052', '-0.1768', '0.2255', '0.2422', '-0.554', '-0.451', '-0.1309', '-0.2507', '0.1576', '-0.196', '0.2052', '0.0774', '0.1832', '-0.3047', '0.08887', '-0.3599', '0.4783', '0.2368', '0.5034', '-0.0008583', '0.01741', '-0.273', '0.1722', '-0.11804', '-0.06146', '-0.252', '0.622', '0.0756', '0.211', '-0.1036', '0.02682', '-0.549', '0.0881', '0.004883', '0.014465', '0.568', '0.09985', '-0.2031', '-0.1526', '0.3728', '-0.553', '0.422', '0.3665', '-0.6436', '-0.517', '0.1211', '0.2424', '0.458', '0.1396', '-0.117', '0.0938', '0.296', '0.1781', '0.208', '-0.1602', '-0.10114', '-0.2805', '-0.0816', '0.1659', '-0.255', '0.1716', '-0.1235', '0.2375', '0.011734', '-0.258', '0.2047', '0.05493', '0.2357', '0.02972', '-0.1823', '0.0229', '-0.1533', '0.1526', '-0.1622', '0.571', '-0.0227', '0.0806', '0.4868', '-0.2443', '-0.2095', '0.8257', '-0.0014305', '0.06058', '-0.2676', '-0.1194', '0.2126']",,,C537070,,,,
mondo:0009240,formiminoglutamic aciduria,"['Formiminoglutamicaciduria (FIGLU-Uria)', 'FTCD deficiency', 'Arakawa syndrome 1', 'formiminotransferase deficiency syndrome', 'formiminoglutamic aciduria', 'formiminoglutamic acidemia', 'formiminotransferase deficiency', 'glutamate formiminotransferase deficiency', 'formiminotransferase cyclodeaminase deficiency', 'Figlu-Uria']",0111679,229100,51208,C0268609,"['-0.4463', '0.0759', '0.0697', '-0.1611', '0.255', '0.02039', '-0.4937', '0.4756', '-0.05426', '-0.1163', '-0.581', '-0.1272', '0.2622', '-0.1401', '-0.2935', '-0.1533', '0.1654', '-0.06158', '-0.52', '-0.6772', '0.2072', '-0.06366', '0.4097', '-0.3362', '0.02605', '-0.2834', '0.1477', '-0.02087', '-0.007645', '-0.1665', '0.3755', '-0.2113', '0.3516', '0.523', '-0.2935', '-0.2805', '-0.4502', '-0.39', '-0.3357', '-0.1544', '0.2008', '-0.5557', '0.213', '-0.3442', '-0.3215', '-0.3157', '0.2698', '-0.1511', '-0.3792', '-0.0829', '-0.1658', '-0.06195', '0.0653', '-0.1368', '0.2954', '-0.03265', '0.2079', '-0.3015', '-0.2062', '0.3933', '-0.1721', '-0.1666', '0.4746', '-0.1957', '0.1442', '-0.0174', '0.1663', '0.291', '-0.693', '0.1351', '0.0816', '0.1532', '-0.4746', '-0.1189', '-0.0999', '0.2292', '0.224', '-0.1486', '0.039', '-0.2742', '0.4763', '0.06046', '0.11816', '0.451', '0.398', '0.3557', '-0.257', '0.3853', '0.524', '0.2162', '0.3284', '0.5537', '-0.3699', '-0.308', '0.4368', '0.383', '0.00452', '-0.4116', '0.0713', '0.1215']",,,C537425,270.8,,,
mondo:0009241,fountain syndrome,"['fountain syndrome', 'intellectual disability, deafness, skeletal abnormalities, coarse face with full lips', 'deafness-skeletal dysplasia-lip granuloma syndrome', 'deafness-skeletal dysplasia-coarse face with full lips syndrome', 'deafness, skeletal dysplasia, lip granuloma', 'intellectual disability, sensorineural deafness, skeletal abnormalities, and coarse face with full lips', 'mental retardation, sensorineural deafness, skeletal abnormalities, and coarse face with full lips']",,229120,3219,C0795944,,,,C537270,,,,
mondo:0009242,brittle cornea syndrome,"['Ehlers-Danlos syndrome type 6B (formerly)', 'type VIB Ehlers-Danlos syndrome', 'BCS1', 'brittle cornea syndrome 1', 'EDS VIB (formerly)', 'brittle cornea syndrome type 1', 'brittle cornea syndrome 2', 'kyphoscoliosis type']",14775,,90354,C0268342,"['-0.3113', '-0.2856', '-0.04572', '-0.2568', '0.3242', '-0.4011', '0.0666', '0.53', '-0.3079', '0.1759', '-0.3447', '-0.247', '-0.3418', '0.137', '-0.1711', '0.0809', '0.3665', '0.4214', '0.0708', '-0.9106', '-0.00367', '0.2357', '0.4111', '-0.05954', '-0.2517', '0.398', '0.046', '0.2078', '0.2888', '0.2488', '0.1552', '0.1287', '0.268', '0.565', '-0.0959', '-0.0234', '0.2185', '-0.4011', '-0.418', '-0.3025', '0.3687', '-0.4429', '0.09576', '0.3765', '-0.11847', '-0.05157', '-0.009544', '0.1984', '0.3875', '0.005184', '0.01782', '-0.04572', '0.712', '-0.02335', '-0.2361', '-0.3093', '0.0763', '-0.1805', '0.0517', '-0.1797', '0.03793', '-0.2659', '-0.333', '-0.004852', '-0.01146', '0.04227', '0.03894', '0.8877', '-0.4502', '0.59', '-0.4966', '0.1296', '-0.002333', '-0.1921', '-0.1581', '-0.55', '0.3057', '0.2118', '0.0339', '-0.1255', '-0.2966', '-0.2462', '-0.5063', '0.6533', '-0.1244', '-0.2208', '0.162', '0.65', '0.2725', '-0.02145', '0.4062', '0.6035', '0.2021', '0.2888', '0.3901', '0.03098', '0.691', '-0.2096', '0.2234', '0.4004']",,,C536198,,,,
mondo:0009243,Fraser-like syndrome,"['Fraser-like syndrome', 'Fused eyelids, airway anomalies, ovarian cysts, and digital anomalies']",,229230,2051,CN200837,,,,C565562,,,,
mondo:0009244,"Freesia Flowers, inability to smell","['Freesia Flowers, inability to smell']",,229250,,,,,,,,,,
mondo:0009246,Friedreich ataxia and congenital glaucoma,['Friedreich ataxia and congenital glaucoma'],,229310,,C1856688,,,,C538061,,,,
mondo:0009247,frontofacionasal dysplasia,"['Frontofacionasal dysostosis', 'Gollop syndrome', 'Ffnd', 'frontofacionasal dysplasia', 'fronto-facio-nasal dysostosis', 'fronto-facio-nasal dyplasia']",,229400,1791,C2931720,,,,C538063,,,,
mondo:0009248,fructose and galactose intolerance,['fructose and galactose intolerance'],,229500,,C1856686,,,,C565558,,,,
mondo:0009249,hereditary fructose intolerance,"['hereditary fructose intolerance syndrome', 'hereditary fructosemia', 'aldolase B deficiency', 'hereditary fructose-1-phosphate aldolase deficiency', 'fructose intolerance', 'fructose-1-phosphate aldolase deficiency', 'fructosemia', 'fructose intolerance, hereditary', 'fructose-1,6-bisphosphate aldolase B deficiency', 'Fructosaemia', 'Aldob deficiency']",9869,229600,469,C0016751,"['-0.001017', '0.688', '-0.309', '-0.07355', '-0.437', '-0.4182', '0.0712', '0.8022', '0.0633', '0.7056', '0.2805', '0.0721', '0.1985', '-0.10205', '-0.852', '0.0816', '-0.598', '-0.805', '-0.547', '-0.8545', '-0.2878', '-0.1492', '0.4492', '-0.5635', '-0.485', '0.1109', '-0.05374', '-0.2917', '-0.1006', '-0.4587', '0.201', '-0.1694', '-0.472', '0.281', '-0.5825', '0.008644', '-0.3708', '-0.522', '0.0387', '0.2734', '-0.1094', '-0.516', '0.3833', '-0.0444', '-0.4214', '0.02335', '-0.3374', '-0.5386', '0.1687', '0.837', '0.06635', '0.719', '0.5894', '-0.0939', '-0.1414', '-0.371', '0.5566', '0.1837', '-0.8022', '0.4927', '0.1122', '-0.2637', '0.2216', '-0.4065', '0.4436', '0.8447', '1.19', '0.05313', '0.04788', '0.0891', '-0.06235', '0.1946', '0.114', '-0.2532', '0.2896', '0.593', '-0.03827', '-0.2086', '0.1322', '0.2837', '-0.1614', '-0.3672', '-0.336', '-0.0739', '0.5444', '0.732', '0.33', '-0.6455', '1.121', '-0.8', '-0.1053', '-0.3003', '-0.447', '-0.08545', '0.2976', '0.4595', '0.2056', '-0.4062', '-0.2205', '0.1434']",C84720,,,271.2,E74.12,10019878,
mondo:0009251,"fructose-1,6-bisphosphatase deficiency","['baker-Winegrad disease', 'FBP1D', 'fructose 1 phosphate aldolase deficiency', 'fructose 1,6 diphosphatase deficiency', 'fructose-1,6-bisphosphatase deficiency', 'fructose-1,6-diphosphatase deficiency']",5204,229700,348,C0016756,"['0.1164', '0.06683', '-0.7935', '-0.1412', '0.328', '-0.4595', '-0.3352', '0.838', '0.358', '0.3384', '0.0963', '0.1273', '0.1877', '0.05518', '-0.3352', '0.3872', '-0.10175', '-0.4207', '-0.1984', '-0.6265', '-0.2266', '-0.7217', '0.546', '-0.423', '-0.4875', '-0.4346', '-0.6084', '-0.4001', '-0.148', '-0.706', '-0.0829', '0.1349', '-0.0982', '0.53', '-0.549', '0.1495', '-0.07623', '-0.0578', '-0.4873', '0.326', '-0.2048', '-0.4463', '0.375', '0.276', '-0.2034', '-0.2563', '-0.3313', '0.1354', '-0.06384', '0.9443', '-0.4854', '-0.1823', '0.4224', '-0.0858', '0.6494', '-0.01038', '0.8193', '-0.3247', '-0.3552', '0.2744', '-0.05936', '0.8887', '0.646', '-0.234', '0.3582', '0.091', '0.78', '0.3125', '-0.488', '0.535', '0.2262', '0.2113', '-0.1192', '-0.3213', '-0.1685', '0.03577', '-0.1962', '-0.1466', '-0.4436', '-0.1185', '0.192', '0.03998', '0.06152', '0.03842', '0.8184', '0.6826', '0.1792', '-0.1609', '0.6377', '-0.2974', '0.662', '0.2634', '-0.3528', '-0.2201', '0.4646', '0.4312', '0.3398', '-0.5234', '-0.4297', '-0.4717']",C128119,,,,,,
mondo:0009252,essential fructosuria,"['hepatic fructokinase deficiency', 'ketohexokinase deficiency', 'fructosuria, essential', 'fructokinase deficiency']",0111680,229800,2056,C0268160,"['-0.2262', '0.244', '-0.0652', '-0.1343', '-0.1625', '-0.2935', '-0.408', '0.06946', '0.04514', '-0.0443', '0.07904', '-0.03038', '0.4478', '-0.095', '-0.3452', '0.3838', '-0.1371', '-0.1108', '-0.3499', '-0.8525', '-0.1929', '-0.3062', '0.6626', '0.2834', '-0.247', '0.08026', '-0.1788', '-0.4775', '-0.0819', '-0.3923', '-0.1548', '0.1122', '0.0428', '0.1276', '-0.5464', '-0.0272', '-0.026', '0.0951', '0.01869', '-0.3975', '0.4536', '-0.453', '0.7603', '-0.00661', '0.08044', '-0.3257', '0.000806', '0.2002', '0.461', '0.3718', '-0.00352', '-0.298', '0.2869', '-0.04764', '-0.0947', '0.05798', '0.5747', '-0.3645', '-0.6777', '0.0726', '0.4634', '0.356', '0.1975', '-0.4922', '0.256', '0.149', '0.5703', '-0.1759', '-0.2493', '0.2673', '-0.343', '-0.11926', '0.1182', '0.0734', '0.243', '0.653', '-0.235', '0.0675', '-0.3025', '0.04437', '0.1655', '0.02766', '-0.0268', '-0.0912', '0.2678', '0.4487', '0.1322', '-0.1643', '0.5967', '-0.0705', '-0.1432', '0.2462', '-0.261', '-0.04642', '0.2544', '0.3577', '0.09674', '-0.5166', '-0.10004', '0.1545']",,,C538068,,E74.11,10015487,
mondo:0009253,Fryns syndrome,"['FRNS', 'diaphragmatic hernia, abnormal face, and distal limb anomalies', 'Moerman Van den Berghe Fryns syndrome', 'diaphragmatic hernia-abnormal face-distal limb anomalies syndrome', 'Fryns syndrome']",,229850,2059,C0220730,,C98932,,C538070,759.89,,,
mondo:0009254,fucosidosis,"['Alpha-L-fucosidase deficiency', 'A-fucosidase deficiency', 'fucosidosis', 'alpha fucosidase deficiency', 'lysosomal storage disease caused by defective alpha-L-fucosidase with accumulation of fucose in the tissues']",14500,230000,349,C0016788,"['-0.2225', '0.4307', '0.4478', '-0.5303', '-0.00826', '-0.3276', '0.1606', '0.1094', '-0.1597', '0.03032', '-0.3484', '0.1688', '-0.005455', '-0.02768', '-0.1946', '0.1179', '0.2177', '0.05643', '-0.5615', '-0.374', '0.03586', '-0.2139', '0.4814', '0.04037', '-0.03583', '-0.144', '0.03195', '-0.0573', '0.01839', '-0.1147', '0.2468', '0.2462', '0.356', '0.1418', '-0.03366', '-0.2207', '-0.4941', '-0.1791', '-0.295', '-0.1265', '-0.1138', '-0.2318', '0.3728', '0.1736', '-0.1075', '-0.4285', '0.1315', '-0.0585', '-0.2317', '0.1268', '-0.1422', '0.4534', '-0.063', '-0.0751', '0.1559', '-0.7505', '-0.07996', '-0.2524', '-0.1764', '-0.1031', '0.181', '0.1554', '-0.06195', '-0.06854', '0.213', '-0.1477', '0.4138', '0.0511', '-0.1884', '0.0731', '-0.5537', '-0.1234', '-0.05453', '0.008415', '0.1697', '0.02731', '0.474', '-0.02519', '-0.02783', '-0.0774', '0.115', '-0.1277', '-0.2334', '0.3599', '0.1757', '0.03638', '0.2411', '0.2917', '0.3628', '0.1277', '0.3198', '0.6357', '-0.05673', '0.1342', '0.654', '0.793', '0.2281', '-0.1735', '0.2703', '0.07874']",C61274,,D005645,271.8,,,
mondo:0009255,galactokinase deficiency,"['GALK deficiency', 'GALK-D', 'galactokinase deficiency', 'Galk deficiency', 'galactosemia II', 'galactokinase deficiency with cataracts', 'hereditary galactokinase deficiency', 'galactosemia 2', 'galactokinase deficiency galactosemia', 'galactosemia type 2']",14695,230200,79237,C0268155,"['-0.608', '0.2124', '0.04376', '0.218', '0.4077', '-0.475', '-0.4082', '0.996', '-0.0316', '-0.04315', '-0.4263', '-0.3025', '-0.1367', '0.3403', '-0.04932', '0.2324', '0.646', '0.2186', '-0.2683', '-0.8823', '-0.269', '-0.31', '0.4543', '-0.05035', '0.135', '0.2157', '-0.04706', '0.1729', '-0.06195', '0.435', '0.7954', '0.10913', '0.422', '0.4182', '-0.921', '0.6987', '-0.2448', '-0.1733', '-0.3708', '0.002562', '0.1022', '-0.1185', '0.253', '0.3933', '0.007027', '-0.1494', '-0.0059', '-0.298', '0.5635', '0.253', '0.2411', '-0.3193', '-0.178', '-0.699', '0.06415', '-0.1097', '0.6577', '-0.1561', '-0.323', '0.2383', '-0.01405', '-0.05176', '0.2234', '-0.3237', '0.4421', '0.2092', '0.55', '0.0787', '-0.1758', '0.3447', '-0.2241', '0.2213', '0.243', '-0.2384', '0.255', '0.1884', '0.1545', '0.1779', '-0.08954', '0.134', '-0.327', '-0.2532', '0.1343', '-0.0973', '0.1509', '0.5566', '0.1293', '-0.1353', '0.7417', '0.3425', '0.1884', '1.043', '-0.0944', '-0.00908', '0.1934', '0.4219', '0.1147', '-0.0915', '0.05902', '-0.01113']",C114767,,,,,,
mondo:0009256,galactorrhea,"['galactorrhea', 'galactorrhea (disease)']",,230300,,,,C113343,,D005687,611.6,,,0100829
mondo:0009257,galactose epimerase deficiency,"['GALE-D', 'uridine diphosphate galactose-4-epimerase deficiency', 'UDP-galactose-4-epimerase deficiency', 'Gale deficiency', 'GALE deficiency', 'galactose epimerase deficiency', 'galactosemia 3', 'epimerase deficiency galactosemia', 'galactosemia type 3']",0111458,230350,79238,,"['-0.0895', '0.2269', '0.299', '0.05865', '0.2102', '-0.2244', '-0.4316', '0.4646', '0.1877', '0.1868', '-0.1015', '-0.0871', '-0.357', '0.06573', '0.04135', '-0.1896', '0.1376', '-0.1895', '-0.4001', '-0.8135', '-0.2268', '-0.2786', '0.714', '-0.03043', '-0.1539', '-0.07605', '0.0607', '-0.1877', '0.312', '0.1614', '0.2754', '-0.1123', '0.1305', '0.2191', '-0.3013', '0.02528', '-0.4893', '-0.02513', '-0.1349', '0.3281', '-0.2625', '-0.366', '0.04062', '-0.0326', '-0.2869', '-0.1021', '0.1663', '-0.1753', '0.2634', '0.3027', '0.1813', '0.1823', '0.03638', '-0.2261', '-0.2062', '0.2837', '0.09607', '-0.4336', '-0.4805', '0.389', '-0.103', '-0.2123', '0.342', '-0.1974', '0.349', '0.3398', '0.0697', '0.08344', '-0.3193', '0.4702', '-0.3325', '0.1907', '-0.05954', '-0.3098', '0.2834', '0.2788', '0.2854', '-0.663', '-0.1581', '-0.0873', '-0.3992', '-0.4204', '-0.2566', '-0.02534', '0.358', '0.3044', '-0.0468', '-0.06168', '0.6763', '0.318', '0.4246', '0.505', '-0.511', '0.1326', '0.159', '0.552', '0.05414', '-0.2153', '0.425', '0.2402']",,,,,,,
mondo:0009258,classic galactosemia,"['galactosemia', 'galactosemia, classic', 'Galt deficiency', 'galactosemia, Duarte variant', 'galactose-1-phosphate uridylyltransferase deficiency', 'galactosemia type 1', 'GALT deficiency', 'galactose-1-phosphate uridyltransferase deficiency', 'transferase deficiency']",0111459,230400,79239,,"['0.1669', '-0.0813', '0.0737', '0.01797', '0.4148', '-0.1687', '-0.482', '0.842', '0.1477', '-0.2278', '-0.2294', '-0.619', '-0.524', '0.3481', '0.04443', '0.02794', '0.002731', '0.126', '-0.4993', '-0.947', '-0.316', '-0.7236', '0.506', '-0.2825', '0.2185', '-0.528', '-0.6025', '0.3677', '-0.2944', '-0.2783', '0.7007', '-0.3633', '0.517', '-0.298', '-0.3909', '0.3188', '-0.01593', '-0.635', '0.2301', '0.1399', '-0.5044', '0.2559', '-0.06113', '-0.09393', '0.0721', '-0.3633', '0.1993', '-0.1256', '-0.0882', '0.631', '0.1608', '0.1494', '0.04004', '-0.1923', '-0.5273', '0.0896', '0.2976', '-0.0207', '-0.5273', '0.1885', '0.4954', '0.1508', '0.473', '-0.11914', '0.2368', '0.3523', '-0.0946', '0.03555', '-0.4302', '-0.10974', '0.0495', '-0.04013', '-0.2147', '-0.269', '-0.1855', '-0.208', '0.541', '-0.508', '0.10986', '-0.348', '-0.02478', '-0.3022', '-0.651', '0.1678', '0.006893', '0.6606', '-0.01147', '-0.714', '1.319', '0.05396', '0.1947', '0.3635', '-0.2605', '-0.0801', '0.1737', '0.517', '0.3628', '0.337', '0.1785', '0.1532']",,,,,,,
mondo:0009259,gamma-glutamylcysteine synthetase deficiency,"['rare inborn error of glutamate-cysteine ligase activity', 'hemolytic anemia due to gamma-glutamylcysteine synthetase deficiency', 'inborn glutamate-cysteine ligase activity disorder', 'hemolytic anaemia due to gamma-glutamylcysteine synthetase deficiency', 'gamma-glutamylcysteine synthetase deficiency, hemolytic anemia due to', 'glutamate-cysteine ligase deficiency', 'inborn error of glutamate-cysteine ligase activity', 'gamma-glutamylcysteine synthetase deficiency, hemolytic anaemia due to']",0111681,230450,33574,,"['-0.4675', '0.1432', '-0.3074', '0.2084', '0.3618', '-0.5566', '-0.571', '0.3862', '0.42', '-0.03995', '0.1486', '0.03354', '0.2644', '0.0715', '0.0547', '-0.1383', '-0.3125', '-0.4094', '-0.24', '-0.8', '0.1707', '-0.1486', '0.757', '-0.2583', '-0.1301', '-0.6255', '-0.4565', '-0.02745', '-0.08716', '-0.5703', '0.24', '-0.05856', '-0.1774', '0.3276', '-0.1063', '-0.616', '-0.2556', '-0.688', '-0.1169', '-0.0404', '0.2106', '-0.6113', '0.0497', '-0.2374', '0.242', '-0.09296', '-0.011345', '-0.1935', '-0.0556', '-0.0767', '-0.2114', '-0.26', '0.1002', '0.3323', '0.1349', '0.061', '0.36', '-0.0557', '-0.481', '0.5386', '0.2104', '0.2086', '0.5894', '-0.18', '-0.0924', '0.0777', '0.2908', '0.3733', '-0.04483', '0.273', '-0.2468', '-0.396', '-0.4229', '-0.1652', '0.02603', '0.3882', '0.02437', '-0.4302', '0.0722', '0.0378', '0.29', '0.0781', '0.1653', '0.1646', '0.11475', '0.1098', '-0.0767', '0.1693', '0.4167', '0.1318', '0.791', '0.1236', '0.06506', '-0.6104', '0.3389', '0.725', '0.1426', '-0.6934', '0.1498', '-0.3105']",,,C565557,270.8,,,
mondo:0009260,GM1 gangliosidosis type 1,"['gangliosidosis, generalized GM1, type 1', 'Glb1 deficiency', 'infantile GM1 gangliosidosis', 'GM1-gangliosidosis, type I, with Cardiac involvement', 'gangliosidosis, generalised GM1, type 1', 'Beta galactosidase deficiency type 1', 'gangliosidosis, generalised GM1, type I, with Cardiac involvement', 'GM1-gangliosidosis, type I', 'GLB deficiency type 1', 'Beta-galactosidase-1 deficiency', 'gangliosidosis generalised GM1 infantile form', 'Norman-Landing disease', 'gangliosidosis generalized GM1 type 1', 'GM1-gangliosidosis, type 1', 'gangliosidosis, generalized GM1, infantile form', 'gangliosidosis generalized GM1 infantile form', 'gangliosidosis generalised GM1 type 1', 'gangliosidosis, generalised GM1, infantile form', 'gangliosidosis, generalized GM1, type I, with Cardiac involvement']",0080502,230500,79255,,"['0.06274', '0.8306', '-0.0555', '-0.0766', '0.077', '-0.736', '0.2976', '0.4387', '-0.2842', '-0.1687', '-0.639', '0.04575', '-0.1953', '0.1501', '0.1936', '-0.08014', '0.5845', '-0.1539', '-0.4583', '-0.657', '0.1381', '-0.218', '0.852', '-0.5776', '-0.0748', '0.045', '0.2996', '-0.0553', '0.01135', '0.3208', '0.8516', '0.3936', '0.6836', '0.09485', '0.0739', '0.02493', '-0.5547', '-0.3833', '-0.6045', '0.693', '0.1836', '-0.596', '0.2698', '0.04654', '0.4236', '-0.03616', '0.5093', '0.05054', '0.0187', '0.1593', '-0.08936', '0.1542', '-0.2847', '-0.3179', '0.1616', '-0.4912', '0.2', '-0.4966', '-0.3835', '-0.0929', '-0.2122', '-0.2212', '0.412', '-0.3235', '0.00832', '-0.1862', '0.693', '-0.3262', '-0.524', '0.187', '-0.3135', '-0.2316', '0.2559', '-0.2042', '-0.1707', '0.335', '0.1578', '-0.193', '-0.705', '0.071', '0.3635', '-0.3462', '-0.5684', '0.278', '0.0727', '-0.219', '-0.02322', '0.3367', '0.466', '0.1445', '0.328', '0.794', '0.173', '-0.1322', '0.306', '0.464', '0.3982', '-0.0002351', '0.6025', '-0.09717']",,,,,,,
mondo:0009261,GM1 gangliosidosis type 2,"['late-infantile GM1 gangliosidosis', 'juvenile GM1 gangliosidosis', 'gangliosidosis generalized GM1 juvenile type', 'gangliosidosis generalized GM1 type 2', 'gangliosidosis, generalized GM1, juvenile type', 'gangliosidosis, generalized GM1, type 2', 'GM1-gangliosidosis, type II', 'gangliosidosis, generalized GM1, late-infantile type', 'GM1-gangliosidosis, type 2', 'gangliosidosis, generalised GM1, juvenile type', 'gangliosidosis, generalised GM1, late-infantile type', 'gangliosidosis generalised GM1 type 2', 'gangliosidosis generalised GM1 juvenile type', 'gangliosidosis, generalised GM1, type 2']",0080501,230600,79256,,"['0.08234', '0.751', '-0.00602', '-0.0395', '0.1003', '-1.041', '0.2026', '0.924', '-0.606', '0.1133', '-0.10297', '0.4695', '-0.2103', '0.1736', '0.63', '0.1947', '0.6577', '-0.2108', '-0.503', '-0.3906', '-0.2426', '-0.2012', '0.7573', '-0.02533', '0.2544', '-0.449', '0.2502', '0.2688', '-0.673', '-0.02243', '0.579', '0.0803', '0.555', '-0.1993', '-0.2751', '-0.0917', '-0.5327', '-0.1236', '-0.653', '0.6016', '-0.1284', '-0.31', '-0.5083', '-0.01993', '-0.03995', '0.258', '0.295', '0.0903', '-0.3394', '-0.2023', '0.1487', '0.0678', '-0.08777', '-0.4224', '0.148', '-0.1753', '0.3054', '-0.1722', '-0.4717', '-0.2058', '-0.514', '-0.0452', '0.7544', '0.0778', '-0.2278', '-0.3418', '0.4346', '-0.11633', '-0.681', '0.324', '0.014565', '-0.1272', '0.282', '0.0418', '0.507', '0.549', '-0.1815', '0.0963', '-0.7397', '0.04028', '0.3022', '-0.6577', '-0.1564', '0.1295', '0.02296', '0.1211', '0.1454', '0.2263', '0.5835', '-0.1792', '0.321', '0.768', '-0.04233', '0.02487', '0.1512', '0.534', '-0.0262', '-0.198', '0.4119', '0.425']",,,,,,,
mondo:0009262,GM1 gangliosidosis type 3,"['gangliosidosis, generalised GM1, chronic type', 'gangliosidosis generalized GM1 chronic type', 'GM1-gangliosidosis, type III', 'gangliosidosis, generalised GM1, type 3', 'adult-onset GM1 gangliosidosis', 'gangliosidosis, generalised GM1, adult type', 'gangliosidosis, generalized GM1, adult type', 'Beta-galactosidase deficiency type 3', 'gangliosidosis, generalized GM1, type 3', 'adult GM1 gangliosidosis', 'gangliosidosis GM1 type 3', 'gangliosidosis, generalized GM1, chronic type', 'GM1-gangliosidosis, type 3', 'gangliosidosis generalised GM1 chronic type']",0080489,230650,79257,,"['0.2947', '0.628', '-0.327', '0.1532', '0.418', '-0.7114', '-0.06903', '0.878', '-0.2695', '-0.4377', '0.06165', '0.448', '-0.2008', '0.12103', '0.757', '-0.278', '0.4531', '-0.4927', '-0.656', '-0.3723', '-0.2607', '-0.076', '0.7227', '-0.2234', '-0.05627', '-0.1373', '0.2944', '-0.1469', '-0.6743', '0.4287', '0.4856', '-0.1152', '0.4368', '0.3455', '-0.002728', '-0.1962', '-0.3164', '-0.4985', '-0.4038', '0.4077', '0.2866', '-0.4136', '0.01743', '0.1903', '-0.1133', '0.1322', '0.3735', '0.4763', '0.003002', '-0.5054', '0.638', '0.3691', '-0.286', '-0.3706', '0.1415', '-0.0329', '0.2173', '-0.769', '-0.05847', '0.2053', '0.1315', '0.1439', '0.2937', '-0.2354', '-0.03336', '-0.08026', '-0.03058', '0.2488', '-0.2126', '0.2935', '-0.2019', '0.1818', '0.387', '-0.1277', '0.226', '0.5464', '-0.362', '-0.010895', '-0.631', '0.393', '-0.0807', '-0.646', '-0.663', '0.7563', '0.2786', '0.201', '-0.0701', '0.03186', '0.907', '0.0385', '0.3833', '0.617', '-0.4346', '-0.1068', '0.2566', '-0.1011', '0.787', '-0.10535', '0.0775', '0.3347']",,,,,,,
mondo:0009263,GAPO syndrome,"['Growth retardation, alopecia, pseudoanodontia, and optic atrophy', 'gapo syndrome', 'Growth delay-alopecia-pseudoanodontia-optic atrophy syndrome', 'Growth retardation, alopecia, pseudoanodontia and optic atrophy']",0112249,230740,2067,,"['-0.337', '-0.4783', '-0.03775', '-0.2385', '0.1549', '-0.2903', '0.1406', '1.375', '-0.4773', '-0.0367', '-0.0931', '-0.2869', '0.00635', '-0.0936', '-0.4998', '0.2452', '0.6353', '0.01573', '-0.3516', '-0.7007', '-0.1046', '-0.1582', '-0.2296', '0.1602', '0.4797', '0.1069', '-0.4746', '0.921', '0.3308', '0.00435', '1.029', '0.0802', '0.1371', '0.00663', '0.0659', '-0.02646', '0.3423', '-0.03046', '-0.2969', '0.5527', '0.499', '-0.286', '0.4563', '0.1921', '0.3604', '-0.11475', '0.1619', '-0.013596', '-0.0543', '-0.694', '-0.3271', '0.02942', '0.117', '0.591', '-0.4023', '-0.08435', '0.491', '-0.1774', '-0.0886', '-0.04422', '0.09686', '0.5176', '-0.2279', '-0.1417', '-0.165', '-0.2542', '0.1897', '0.4575', '-0.2627', '0.7236', '-0.3184', '-0.1071', '0.10114', '-0.4858', '-0.0982', '-0.3167', '0.518', '0.1901', '-0.3027', '0.6597', '0.3306', '-0.2279', '0.11127', '0.2258', '-0.1711', '0.1865', '0.07153', '0.8887', '-0.06836', '0.1812', '0.2646', '0.09875', '0.4304', '0.2725', '1.141', '-0.10156', '0.552', '-0.03958', '0.891', '0.4087']",,,C535642,,,,
mondo:0009264,gastroschisis,"['eventration', 'gastroschisis', 'abdominal wall defects', 'laparoschisis', 'congenital fissure of the abdominal cavity']",11044,230750,2368,C0265706,,C84725,1000949,D020139,756.73,Q79.3,10018046,
mondo:0009265,Gaucher disease type I,"['Gba deficiency', 'non-cerebral juvenile Gaucher disease', 'Gd 1', 'Gaucher disease type 1', 'acid Beta-glucosidase deficiency', 'Gaucher disease, type 1', 'Gaucher disease, type I', 'Gaucher^s disease type I', 'GD I', 'Gaucher disease, noncerebral juvenile']",0110957,230800,77259,,"['0.06665', '0.673', '-0.07745', '-1.146', '-0.05286', '-0.2491', '-0.02577', '0.8975', '-1.146', '-0.3103', '-0.1528', '-0.068', '-0.242', '0.897', '-0.05804', '-0.4888', '0.00945', '-0.0351', '-0.4824', '-0.389', '-0.3303', '-0.614', '0.541', '-0.643', '-0.11426', '-0.03912', '0.2032', '0.3796', '0.1879', '-0.3474', '0.4185', '0.06085', '0.278', '0.2124', '0.2961', '-0.0832', '-0.4595', '-0.4556', '0.1261', '-0.2046', '0.384', '-0.2074', '0.161', '-0.551', '-0.2632', '0.3384', '-0.3176', '-0.401', '-0.1417', '0.1179', '0.5586', '0.0931', '0.829', '-0.4978', '0.668', '-0.575', '-0.2004', '0.04208', '0.0428', '0.149', '-0.1306', '0.001999', '-0.02362', '-1.027', '0.1624', '0.3633', '-0.1542', '0.1132', '-0.4504', '-0.373', '0.1433', '0.11066', '-0.02362', '-0.1323', '0.7026', '0.1464', '-0.2273', '-0.099', '-0.1671', '-0.6133', '-0.1589', '-0.998', '0.1971', '-0.4185', '-0.8374', '-0.4465', '0.799', '0.0964', '0.1777', '0.1626', '0.2316', '-0.535', '-0.3518', '-0.03525', '0.9863', '1.285', '-0.2133', '-0.2795', '0.5225', '-0.8887']",,,,,,,
mondo:0009266,Gaucher disease type II,"['Gaucher disease, type 2', 'Gaucher disease, infantile cerebral', 'Gd 2', 'GD II', 'Gaucher^s disease type II', 'Gaucher disease, type II', 'infantile cerebral Gaucher disease', 'Gaucher disease type 2', 'Gaucher disease, acute neuronopathic type', 'acute neuronopathic Gaucher disease']",0110958,230900,77260,,"['-0.05756', '0.8457', '0.07355', '-0.7124', '-0.263', '-0.6396', '0.0682', '0.933', '-1.268', '-0.3838', '-0.1907', '-0.07', '-0.10803', '0.7554', '0.378', '-0.4229', '0.10455', '0.2485', '-0.2089', '-0.855', '-0.5435', '-0.753', '0.3945', '-0.3665', '0.11774', '0.0572', '0.2383', '0.5815', '0.3225', '-0.146', '0.4744', '0.11566', '0.5557', '-0.0512', '0.02557', '0.2098', '-0.4568', '-0.5103', '0.3123', '-0.0865', '0.4705', '-0.538', '-0.0877', '-0.4119', '-0.532', '0.07544', '-0.4841', '-0.178', '-0.2988', '-0.1616', '0.3264', '0.6113', '0.677', '-0.578', '0.3523', '-0.04825', '-0.07074', '0.2401', '0.3118', '-0.2129', '0.05838', '-0.4763', '0.3772', '-0.8306', '-0.0998', '0.3367', '0.012665', '-0.1071', '-0.633', '0.1059', '0.2593', '0.3564', '0.1853', '-0.2944', '0.7373', '0.0608', '0.0644', '0.3396', '-0.03955', '-0.367', '-0.4048', '-1.032', '-0.03275', '-0.2668', '-0.3818', '-0.6772', '0.727', '0.2169', '0.4265', '0.0816', '-0.1423', '-0.3738', '0.11145', '0.1418', '0.2717', '1.375', '-0.2305', '-0.0381', '0.6777', '-0.959']",,,,,,,
mondo:0009267,Gaucher disease type III,"['Gaucher disease, type III', 'Gaucher disease, juvenile and adult, cerebral', 'Gaucher disease, Norrbottnian type', 'Gaucher disease, type 3', 'Gaucher disease, Subacute neuronopathic type', 'Gd 3', 'Gaucher disease, chronic neuronopathic type', 'Gaucher disease, subacute neuronopathic type', 'Gaucher disease, type 3B', 'chronic neuronopathic Gaucher disease', 'Gaucher disease type 3', 'Gaucher disease, type 3A', 'GD III', 'cerebral juvenile and adult form of Gaucher disease', 'Gaucher^s disease type III']",0110959,231000,77261,,"['0.0122', '0.79', '-0.1035', '-0.7524', '-0.1572', '-0.4045', '-0.1304', '0.7373', '-1.257', '-0.467', '-0.467', '0.07825', '-0.1992', '0.714', '0.1588', '-0.6367', '0.3157', '-0.03543', '-0.1885', '-0.5645', '-0.358', '-0.6504', '0.2444', '-0.713', '-0.2025', '0.2013', '0.2023', '0.3027', '0.34', '-0.2235', '0.511', '0.0741', '0.4978', '0.0461', '0.06046', '-0.04855', '-0.7256', '-0.5405', '-0.2076', '-0.2401', '0.504', '-0.343', '-0.07764', '-0.3186', '-0.2505', '0.2256', '-0.3213', '-0.1833', '-0.3865', '0.0001155', '0.697', '0.5957', '0.993', '-0.2732', '0.6406', '-0.4543', '-0.192', '-0.0764', '0.1267', '0.01942', '-0.2365', '0.0678', '0.419', '-1.065', '-0.0796', '0.277', '-0.09894', '0.02896', '-0.5703', '-0.1245', '0.1959', '0.3767', '0.1962', '-0.2305', '0.6416', '0.1487', '-0.3232', '-0.01831', '0.0917', '-0.8223', '-0.3542', '-1.168', '-0.06775', '-0.1621', '-0.6636', '-0.599', '1.017', '0.0638', '0.3413', '0.02623', '0.1161', '-0.547', '-0.3208', '0.1268', '0.848', '1.533', '-0.04474', '0.0805', '0.7983', '-1.044']",,,,,,,
mondo:0009268,Gaucher disease-ophthalmoplegia-cardiovascular calcification syndrome,"['Gaucher disease, type 3C', 'cardiovascular Gaucher disease', 'pseudo Gaucher disease', 'Gaucher-like disease', 'Gaucher disease, type IIIC', 'Gaucher disease - ophthalmoplegia - cardiovascular calcification', 'Gaucher disease type 3C']",0112250,231005,2072,C2931585,"['-0.4646', '0.6865', '-0.2703', '-0.7427', '-0.2832', '-0.1709', '0.1776', '0.8296', '-1.042', '-0.3977', '-0.6147', '-0.3074', '0.1882', '1.048', '-0.03586', '-0.6274', '-0.159', '0.358', '-0.5435', '-0.6777', '-0.3481', '-0.7993', '0.1234', '-0.2299', '-0.0657', '-0.2737', '0.0499', '0.596', '0.8105', '-0.2815', '0.704', '0.2445', '0.3052', '0.2101', '0.4026', '-0.1841', '-0.4695', '-0.8613', '0.2644', '-0.439', '0.58', '-0.2042', '0.00724', '0.10895', '-0.5356', '0.4133', '-0.3677', '-0.203', '-0.2544', '-0.09564', '0.503', '0.3137', '1.013', '-0.1537', '0.3567', '-0.8467', '-0.228', '0.2178', '0.3125', '-0.11255', '0.0967', '-0.2377', '0.253', '-1.085', '0.05267', '0.115', '-0.1521', '-6.58e-05', '-0.9683', '-0.188', '0.1165', '0.05606', '-0.1035', '0.01662', '0.2986', '0.10815', '-0.2322', '0.005447', '-0.0804', '-0.4841', '-0.531', '-0.564', '-0.02954', '-0.1678', '-0.691', '-0.272', '0.763', '0.00914', '0.2705', '0.03336', '-0.04163', '-0.296', '0.1804', '0.5366', '0.688', '0.971', '0.02261', '-0.10205', '0.3657', '-0.8335']",,,C565553,,,,
mondo:0009269,geleophysic dysplasia 1,"['Geleophysic dysplasia type 1', 'geleophysic dysplasia 1', 'GPHYSD1', 'geleophysic dysplasia caused by mutation in ADAMTSL2', 'GELEOPHYSIC dysplasia 1', 'ADAMTSL2 geleophysic dysplasia']",0111725,231050,,C3278147,,,,,,,,
mondo:0009270,genito-palato-cardiac syndrome,"['Gardner-Silengo-Wachtel syndrome', 'GENITOPALATOCARDIAC syndrome', 'Male pseudohermaphroditism with micrognathia, cleft palate, and conotruncal Cardiac defect', 'genito palato cardiac syndrome']",,231060,2075,C1856466,,,,C537683,,,,
mondo:0009271,geroderma osteodysplastica,"['Walt Disney dwarfism', 'GERODERMA OSTEODYSPLASTICUM', 'GO', 'Geroderma osteodysplasticum', 'Gerodermia osteodysplastica']",0111266,231070,2078,C0432255,"['-0.3794', '-0.1943', '0.3103', '-0.1649', '0.204', '-0.3066', '-0.2047', '0.6953', '-0.3245', '-0.1277', '-0.3257', '0.0913', '0.2302', '0.1471', '-0.3193', '0.3174', '0.2827', '0.2341', '-0.2488', '-0.5244', '0.1047', '0.104', '0.508', '-0.261', '0.03168', '0.3054', '0.0979', '0.01787', '0.2734', '0.095', '0.05576', '-0.2668', '0.1711', '0.4314', '0.007668', '-0.109', '0.0457', '-0.6855', '0.07355', '-0.4653', '0.2242', '-0.4497', '-0.11365', '-0.05185', '0.071', '-0.02753', '-0.1946', '0.5933', '-0.1179', '-0.04474', '-0.3315', '0.1968', '0.302', '0.1028', '-0.4832', '0.1231', '-0.2708', '-0.0736', '-0.28', '-0.04675', '0.2032', '-0.1857', '-0.7344', '-0.3206', '-0.1409', '0.07733', '0.01284', '0.634', '0.07446', '0.2168', '-0.4043', '-0.2184', '0.0586', '-0.323', '-0.2489', '0.02538', '0.03207', '-0.2314', '0.1715', '-0.1274', '-0.3286', '-0.04626', '-0.1632', '0.2612', '-0.04706', '0.4243', '-0.0863', '0.3896', '0.2615', '0.1022', '0.2468', '0.3816', '-0.156', '0.004753', '0.3408', '0.2399', '0.1941', '-0.649', '0.4045', '0.02696']",,,C537799,759.89,,,
mondo:0009272,German syndrome,['German syndrome'],,231080,2077,C3887495,,,,C562543,,,,
mondo:0009273,"hydatidiform mole, recurrent, 1","['hydatidiform MOLE, recurrent, 1', 'HYDM1', 'hydatidiform mole, recurrent, 1', 'complete hydatidiform mole caused by mutation in NLRP7', 'NLRP7 complete hydatidiform mole', 'hydatidiform mole', 'hydatidiform Mole, complete', 'gestational trophoblastic disease', 'hydatidiform Mole, recurrent, type 1']",,231090,,C3463897,,,,,,,,
mondo:0009274,ghosal hematodiaphyseal dysplasia,"['Ghosal hematodiaphyseal syndrome', 'GHDD', 'diaphyseal dysplasia-anemia syndrome', 'ghosal hematodiaphyseal dysplasia', 'GHOSAL hematodiaphyseal dysplasia', 'Ghosal hematodiaphyseal dysplasia syndrome', 'Ghosal syndrome']",0112251,231095,1802,,"['-0.09656', '0.131', '0.05008', '-0.0785', '0.3037', '-0.2947', '-0.1354', '0.6636', '0.195', '-0.06683', '0.0302', '-0.03134', '-0.03105', '-0.1443', '0.142', '0.0832', '0.2467', '-0.06854', '-0.2153', '-0.2622', '-0.00119', '-0.1847', '0.607', '-0.2773', '-0.026', '0.02032', '-0.1923', '-0.168', '0.04797', '-0.1848', '0.3645', '-0.2145', '0.1241', '0.1549', '-0.04376', '-0.2328', '0.04803', '-0.5815', '-0.05798', '-0.2408', '-0.01299', '-0.2372', '0.1197', '-0.3523', '-0.1505', '-0.2031', '-0.00891', '0.3032', '-0.02063', '-0.3025', '0.04257', '-0.2014', '0.01312', '0.0836', '-0.1252', '-0.1376', '0.1047', '-0.286', '-0.311', '0.01477', '0.2861', '0.0972', '-0.076', '-0.351', '0.08014', '-0.04987', '0.117', '0.3225', '-0.376', '0.4514', '-0.169', '-0.2927', '-0.02113', '0.1353', '-0.166', '0.2006', '-0.1244', '0.1754', '-0.1818', '-0.1427', '0.00732', '0.03004', '-0.01974', '0.3', '-0.01092', '0.1455', '0.213', '0.3313', '0.2957', '-0.2832', '0.1103', '0.0616', '0.013115', '-0.1587', '0.61', '0.04886', '0.4165', '-0.4702', '0.00667', '-0.1702']",,,C565551,756.59,,,
mondo:0009275,neonatal hemochromatosis,"['hemochromatosis, neonatal', 'neonatal Hepatitis', 'Nhc', 'Nh', 'giant cell Hepatitis, formerly', 'neonatal hepatitis (formerly)', 'giant cell Hepatitis', 'alloimmune Hepatitis, congenital', 'hemochromatosis neonatal', 'giant cell Hepatitis (formerly)', 'neonatal Hepatitis, formerly', 'idiopathic neonatal hemochromatosis']",,231100,446,C0268059,,C129980,,C536394,,,,
mondo:0009276,Bernard-Soulier syndrome,"['Bernard-Soulier syndrome, type C', 'Bernard Soulier syndrome', 'glycoprotein Ib, Platelet, deficiency of', 'deficiency of platelet glycoprotein 1b', 'Hemorrhagiparous thrombocytic dystrophy', 'BSS', 'Von Willebrand Factor receptor deficiency', 'Platelet glycoprotein Ib deficiency', 'bleeding disorder, Platelet-type, 1', 'Bernard-Soulier syndrome, type A1', 'Bernard-Soulier syndrome, type B', 'Bernard-Soulier syndrome, type A1 (recessive)', 'Bernard-Soulier syndrome', 'hemorrhagic dystrophic thrombocytopenia', 'Platelet glycoprotein 1b, deficiency of', 'thrombopathy, Bernard-Soulier', 'macrothrombocytopenia, familial Bernard-Soulier type', 'giant platelet disease', 'Bernard - Soulier thrombopathy', 'giant platelet disorder, isolated', 'giant platelet syndrome']",2217,231200,274,C0005129,"['-0.729', '-0.10187', '0.1141', '-0.2222', '0.1272', '-0.03937', '-0.2673', '0.05545', '0.000685', '-0.07007', '0.2249', '0.0583', '0.10516', '-0.3218', '-0.0623', '-0.1625', '0.1511', '0.2292', '0.0431', '-0.7725', '-0.1005', '-0.1163', '0.5264', '-0.3083', '0.3198', '0.010315', '-0.07587', '0.0188', '0.1655', '0.03366', '0.08496', '0.2113', '0.2175', '0.456', '-0.3232', '-0.2668', '-0.306', '-0.2534', '-0.01616', '-0.4688', '0.2095', '-0.115', '-0.03001', '-0.3267', '-0.199', '-0.422', '-0.3076', '0.157', '0.4934', '-0.05078', '0.1893', '-0.02', '0.142', '0.1777', '-0.4526', '-0.04996', '0.279', '0.05487', '-0.7734', '0.11383', '-0.1307', '0.05493', '0.22', '-0.2488', '0.0867', '-0.01337', '0.1288', '-0.1345', '-0.3948', '0.518', '-0.4', '-0.2832', '-0.1617', '-0.1672', '0.307', '0.06323', '0.586', '0.05658', '0.266', '-0.11395', '-0.4553', '-0.3484', '0.0875', '0.2098', '0.01772', '0.1592', '0.11554', '0.573', '0.2177', '-0.2391', '-0.03827', '0.681', '0.099', '-0.11536', '0.5625', '0.4639', '0.332', '-0.6147', '0.03632', '0.3']",C84595,,D001606,,,10057473,
mondo:0009277,glaucoma 3A,"['glaucoma, congenital', 'GLC3A', 'Primary Congenital glaucoma 3A', 'glaucoma 3, primary congenital, type a', 'glaucoma 3, primary congenital, A', 'glaucoma, primary open angle, adult-onset', 'glaucoma, primary open angle, juvenile-onset', 'simple buphthalmos', 'buphthalmos', 'glaucoma 3A, primary open angle, congenital, juvenile, or adult onset']",11211,231300,98977,,"['0.3394', '-0.2986', '-0.8296', '1.073', '-0.303', '0.06287', '0.02019', '0.933', '-0.3389', '-0.791', '0.4797', '-0.11206', '-0.01238', '0.8633', '-0.969', '-0.3093', '-0.1619', '-0.0866', '0.2732', '-0.514', '0.2556', '0.267', '0.007023', '-0.2146', '-0.0413', '-0.2241', '-0.02043', '0.331', '-0.1903', '0.253', '0.2947', '-0.194', '0.4097', '0.1792', '-0.293', '0.1376', '0.04855', '-0.5513', '0.4426', '-0.593', '0.769', '-0.58', '0.842', '-0.4775', '-0.2542', '1.039', '0.1715', '-0.0578', '0.8394', '-0.1554', '-0.0953', '0.01239', '-0.261', '-1.466', '0.632', '-0.1425', '0.3796', '0.692', '-1.504', '-0.3572', '-0.3604', '-0.09705', '0.1305', '0.4802', '-0.39', '-0.3845', '0.456', '0.743', '-0.2102', '0.773', '0.2458', '0.698', '0.549', '-0.607', '-0.1533', '0.10706', '0.6235', '0.826', '-0.1627', '0.1647', '0.3271', '-0.2656', '-0.376', '0.809', '0.2988', '0.2362', '0.3257', '-0.3071', '0.5527', '0.5737', '-0.04755', '0.3303', '-0.7373', '0.12286', '1.257', '-0.43', '-0.2517', '-0.04318', '-0.1436', '-0.539']",C148260,,,743.21,,,
mondo:0009279,triple-A syndrome,"['quaternary A syndrome', 'Addisonian-achalasia syndrome', '3A syndrome', 'triple-a syndrome', 'glucocorticoid deficiency and achalasia', 'achalasia-alacrima syndrome', 'alacrima-achalasia-adrenal insufficiency neurologic disorder', 'Allgrove syndrome', 'AAAS', 'Double A syndrome', 'AAA syndrome', 'achalasia addisonianism alacrimia syndrome', '4A syndrome', '2A syndrome', 'hypoadrenalism with achalasia', 'ACTH-resistant adrenal insufficiency, achalasia and alacrima', 'achalasia alacrima syndrome', 'AAA', 'Addisonian achalasia syndrome', 'achalasia-addisonianism-alacrima syndrome', 'triple A syndrome', 'adrenal insufficiency-achalasia-alacrima syndrome', 'achalasia-addisonianism-alacrimia syndrome', 'alacrima-achalasia-addisonianism']",0050602,231550,869,,"['-0.295', '0.53', '-0.2076', '-0.1101', '-0.493', '-0.6436', '-0.09094', '0.438', '-0.559', '-0.94', '0.0739', '-0.1411', '-0.439', '0.4688', '-0.1086', '-0.1741', '0.0789', '0.05307', '-0.1166', '-0.5317', '0.379', '-0.142', '0.3328', '0.0955', '0.2686', '0.1316', '0.0422', '0.1741', '0.267', '0.02162', '0.5986', '0.02274', '0.04504', '-0.47', '0.02834', '0.3098', '0.531', '-0.2302', '-0.94', '0.222', '0.2603', '-0.1225', '0.11334', '0.299', '0.1344', '-0.527', '-0.386', '0.0635', '-0.3376', '0.6294', '-0.08997', '0.8022', '-0.4875', '-0.207', '-0.10297', '-0.1814', '0.877', '-0.1598', '0.0128', '0.809', '-0.1466', '0.66', '0.2822', '-0.494', '-0.0941', '0.01328', '0.4468', '0.287', '-0.2742', '0.2673', '-0.9077', '0.114', '0.2961', '0.3381', '0.3733', '-0.413', '0.08594', '0.1356', '0.459', '0.2062', '0.0931', '-0.801', '0.3608', '0.2998', '0.3206', '0.07086', '0.2515', '-0.2064', '0.7817', '-0.6953', '0.1265', '-0.3862', '-0.03543', '-0.6143', '0.6436', '0.319', '0.639', '-0.64', '0.03934', '0.6255']",C131005,1001997,C536008,255.41,,,
mondo:0009280,monosodium glutamate sensitivity,"['Chinese restaurant syndrome', 'monosodium glutamate sensitivity']",,231630,,C0008127,,,,C562377,989.89,,,
mondo:0009281,glutaryl-CoA dehydrogenase deficiency,"['glutaric acidemia type 1', 'GA1', 'glutaryl-coenzyme A dehydrogenase deficiency', 'glutaryl-CoA dehydrogenase deficiency', 'Ga 1', 'glutaric acidemia 1', 'glutaricaciduria, type I', 'glutaric acidemia type I', 'glutaric acidemia I', 'glutaric aciduria 1', 'GCDHD', 'glutaric aciduria, type 1', 'glutaric aciduria type 1']",0111254,231670,25,C0268595,"['0.3677', '0.338', '-0.3828', '0.223', '-0.2625', '-0.346', '-0.03595', '0.4807', '-0.2205', '0.2603', '-0.07135', '0.2297', '0.6514', '-0.2338', '0.03256', '-0.1705', '-0.1385', '-0.1326', '-0.4094', '-0.549', '-0.1421', '-0.8506', '0.0439', '-0.2664', '-0.4495', '-0.6743', '-0.2651', '-0.04715', '-0.442', '-0.04492', '-0.1584', '0.3857', '0.313', '-0.01804', '-0.5757', '0.656', '0.4111', '-0.1461', '-0.07935', '-0.2369', '-0.0357', '-0.814', '0.538', '-0.1713', '0.1406', '-0.251', '-0.416', '-0.0607', '-0.1241', '0.668', '0.2817', '-0.0524', '-0.2164', '-0.7056', '0.512', '-0.2903', '0.5713', '-0.4153', '-0.731', '0.5', '0.1945', '0.503', '0.002403', '-0.2803', '-0.5654', '0.1505', '0.3008', '-0.2874', '-0.4053', '0.0671', '-0.3926', '0.561', '-0.417', '-0.2339', '0.1447', '-0.404', '0.402', '-0.1145', '-0.4094', '-0.1412', '0.03622', '-0.5435', '-0.2357', '0.3757', '0.5244', '0.5127', '-0.3018', '-0.3457', '0.3682', '-0.04974', '0.707', '0.5996', '-0.01072', '-0.541', '0.6797', '-0.00535', '-0.05655', '-0.2961', '0.0684', '-0.288']",C99101,,C536833,,E72.3,,
mondo:0009282,multiple acyl-CoA dehydrogenase deficiency,"['MADD', 'glutaric acidemia 2A', 'glutaric acidemia IIC', 'glutaric acidemia IIB', 'Ga 2', 'multiple acyl Coenzyme A dehydrogenase deficiency', 'EMA', 'glutaric aciduria 2', 'Etfa deficiency', 'glutaric acidemia 2', 'Etfdh deficiency', 'glutaric acidemia 2C', 'glutaric acidemia type II', 'glutaric aciduria type 2', 'glutaric acidemia type 2', 'glutaric aciduria, type 2', 'MAD deficiency', 'Etfb deficiency', 'glutaric acidemia IIA', 'electron transfer flavoprotein deficiency', 'glutaric acidemia 2B', 'electron transfer flavoprotein ubiquinone oxidoreductase deficiency', 'ethylmalonic-Adipicaciduria', 'multiple acyl-CoA dehydrogenase deficiency']",0060358,231680,26791,C0268596,"['0.05582', '0.427', '-0.77', '0.493', '0.4644', '-0.8086', '0.195', '0.497', '-0.2439', '-0.4744', '-0.0333', '-0.4937', '0.742', '0.12305', '-1.205', '-0.1915', '-0.2766', '0.106', '-0.1462', '-0.6626', '0.0136', '-0.359', '1.244', '0.1929', '-0.2988', '-0.08685', '0.02876', '0.0742', '0.11145', '-0.3357', '0.1022', '0.2235', '0.1335', '0.0812', '-0.4443', '-0.2998', '-0.64', '0.07825', '-0.408', '0.433', '-0.2375', '-0.67', '0.2769', '0.04068', '0.3237', '-0.2786', '-0.00964', '0.2798', '0.041', '0.4705', '-0.449', '-0.2383', '0.05682', '0.00115', '0.4158', '-0.908', '-0.0883', '0.00574', '-0.09406', '0.6646', '0.241', '-0.02318', '0.3062', '-0.1875', '-0.487', '0.01546', '0.4673', '0.279', '-0.6704', '0.10736', '0.2676', '0.207', '0.2534', '0.3254', '0.2097', '0.6777', '0.3567', '-0.3926', '-0.2007', '-0.1592', '0.437', '0.192', '-0.2993', '-0.2007', '0.003294', '0.801', '-0.3467', '-0.1489', '0.3608', '-0.1449', '0.3281', '0.558', '0.10834', '0.1644', '-0.0881', '0.4397', '0.0783', '-0.1132', '-0.2266', '0.1035']",C84907,,,,,,
mondo:0009283,glutaric acidemia type 3,"['glutaric acidemia type III', 'glutaryl-Coa oxidase deficiency', 'glutaric aciduria 3', 'SUGCT glutaric aciduria (disease)', 'GA3', 'Ga 3', 'glutaric aciduria III', 'glutaryl-CoA oxidase deficiency', 'GA III', 'glutaric aciduria type III', 'glutaric aciduria type 3']",0112246,231690,35706,C0342873,"['-0.2375', '0.2079', '-0.10004', '0.02957', '0.1356', '-0.4624', '-0.1643', '0.1915', '-0.19', '0.1748', '-0.02946', '-0.2052', '-0.0629', '-0.3293', '0.08954', '0.1741', '0.1477', '-0.05576', '-0.3918', '-0.512', '-0.1412', '-0.312', '0.5776', '-0.1191', '0.0901', '0.1517', '-0.0512', '-0.1309', '0.1428', '-0.02074', '0.2455', '0.1209', '-0.08765', '0.2385', '-0.269', '-0.259', '0.1705', '-0.06525', '0.1189', '-0.2024', '0.1497', '-0.6724', '0.1989', '-0.3235', '-0.1747', '-0.4475', '0.2313', '-0.00974', '-0.0772', '0.1354', '-0.06287', '-0.2303', '-0.09204', '-0.1274', '-0.1569', '-0.2142', '0.4375', '-0.2156', '-0.2844', '0.3274', '0.1628', '-0.1908', '0.3308', '-0.2114', '0.2607', '0.0552', '0.2932', '0.03323', '-0.4219', '0.1619', '-0.33', '-0.0596', '-0.239', '0.1823', '0.1407', '0.3894', '0.1031', '-0.2396', '-0.1836', '0.08685', '0.2947', '0.0872', '-0.23', '0.3176', '0.1613', '0.2568', '0.0003493', '0.01071', '0.4932', '0.2218', '0.3584', '0.09814', '-0.2168', '-0.3176', '0.6655', '0.1943', '0.3274', '-0.514', '0.00651', '-0.097']",,,C562818,270.2,E72.3,,
mondo:0009284,glutathione synthetase deficiency without 5-oxoprolinuria,"['hemolytic anemia due to glutathione synthetase deficiency', 'glutathione synthetase deficiency of erythrocytes, hemolytic anemia due to', 'GSSDE', 'hemolytic anaemia due to glutathione synthetase deficiency', 'glutathione synthetase deficiency of erythrocytes, hemolytic anaemia due to']",0112252,231900,289849,C1856399,"['-0.1669', '0.1096', '-0.07965', '0.003624', '0.09595', '-0.0809', '-0.04962', '0.0721', '-0.03973', '-0.005733', '-0.08276', '-0.04153', '0.03586', '-0.0375', '-0.00971', '-0.0841', '-0.01793', '-0.08997', '-0.11633', '-0.2556', '-0.013405', '-0.05804', '0.1345', '-0.01411', '0.0216', '-0.03168', '0.01994', '-0.01596', '-0.04617', '-0.0584', '0.0856', '0.04474', '0.1254', '0.1096', '-0.0081', '-0.09503', '-0.03726', '-0.09863', '-0.04028', '-0.0626', '0.0439', '-0.1487', '0.06683', '-0.04126', '-0.1161', '-0.09076', '0.02756', '0.03427', '0.0002371', '0.10455', '-0.03114', '-0.0978', '0.0655', '0.02121', '-0.01663', '-0.0439', '0.1742', '-0.0905', '-0.1425', '0.1', '0.102', '0.07623', '0.0691', '-0.00943', '0.03876', '-0.01997', '0.1505', '0.0527', '-0.1304', '0.1343', '-0.0806', '-3.994e-05', '-0.02975', '-0.0945', '0.04718', '0.0648', '0.0384', '-0.02068', '-0.0338', '-0.0257', '0.002373', '-0.03195', '0.01158', '0.05817', '0.0799', '0.03806', '0.01418', '0.0773', '0.1881', '0.02533', '0.11194', '0.0788', '-0.0538', '-0.05402', '0.2384', '0.2028', '0.07916', '-0.2146', '-0.02551', '0.0776']",,,C565545,,,,
mondo:0009285,gamma-glutamyl transpeptidase deficiency,"['rare inborn error of glutathione hydrolase activity', 'gamma-glutamyltranspeptidase deficiency', 'glutathionuria', 'GTG deficiency', 'glutathioninuria', 'GGT1 deficiency', 'gamma-glutamyltransferase deficiency', 'inborn error of glutathione hydrolase activity', 'GGT deficiency']",0111257,231950,33573,C0268524,"['-0.53', '0.2151', '-0.6694', '0.1938', '-0.04407', '-0.01168', '-0.413', '0.5474', '-0.1588', '-0.05002', '-0.2473', '-0.108', '0.07263', '-0.2693', '-0.05914', '0.2603', '0.217', '-0.1865', '-0.5347', '-0.402', '0.1103', '-0.3062', '0.2532', '-0.0853', '-0.2041', '-0.3645', '0.10846', '-0.0357', '-0.0912', '-0.108', '0.4978', '0.1257', '0.2698', '0.2125', '-0.11774', '-0.216', '0.02892', '-0.47', '-0.07086', '-0.096', '0.1671', '-0.4802', '0.3965', '-0.873', '-0.368', '-0.10187', '0.1595', '-0.2495', '-0.2583', '0.09125', '-0.1031', '-0.2068', '0.1162', '-0.0619', '-0.1725', '-0.0464', '0.3218', '-0.2625', '-0.4614', '0.3103', '0.2031', '-0.1047', '0.1495', '-0.1952', '-0.144', '-0.03955', '0.3416', '0.0163', '-0.96', '0.212', '0.04636', '-0.01843', '-0.497', '-0.2129', '0.2822', '0.2084', '0.11786', '0.309', '-0.007336', '-0.005974', '0.2686', '-0.04202', '0.2773', '0.47', '0.1946', '-0.00499', '0.2296', '0.1411', '0.0735', '-0.1071', '0.4377', '0.259', '-0.3225', '-0.3862', '0.782', '0.438', '-0.1995', '-0.5977', '-0.1685', '0.1288']",,,C536836,270.8,,,
mondo:0009286,"gluteal muscles, absence of","['congenital absence of gluteal muscles', 'gluteal muscle, absence of', 'absence of gluteal muscle', 'gluteal muscles, absence of']",,231970,,,,,,C535561,,,,
mondo:0009287,glycogen storage disease due to glucose-6-phosphatase deficiency type IA,"['glycogen storage disease type 1a', 'glucose-6-phosphatase deficiency glycogen storage disease', 'glycogenosis type Ia', 'GSD type 1a', 'GSDIa', 'glycogen storage disease due to G6P deficiency type Ia', 'hepatorenal form of glycogen storage disease', 'glycogenosis due to glucose-6-phosphatase deficiency type 1a', 'glycogen storage disease Ia', 'hepatorenal glycogenosis', 'glucose-6-phosphatase deficiency', 'glycogen storage disease 1', 'GSD due to G6P deficiency type Ia', 'G6P deficiency type 1a', 'G6PC glycogen storage disease', 'glycogen storage disease 1A', 'glycogen storage disease caused by mutation in G6PC', 'GSD due to G6P deficiency type 1a', 'GSD Ia', 'Von Gierke disease', 'GSD1', 'GSD1A', 'glycogenosis due to glucose-6-phosphatase deficiency type Ia', 'glycogen storage disease type Ia']",2749,232200,79258,CN205860,"['0.3018', '-0.08606', '0.03647', '-0.3901', '0.8555', '-0.1006', '0.2335', '0.9434', '-0.2308', '0.05194', '-0.0662', '-0.4348', '-0.1526', '0.07446', '-0.575', '-0.2019', '0.2405', '-0.377', '-0.2474', '-0.1895', '0.545', '-0.08356', '0.844', '-0.381', '-0.5884', '0.03053', '-0.1719', '-0.2134', '-0.00954', '0.303', '0.3037', '-0.04404', '0.1627', '0.0437', '0.1565', '-0.3782', '-0.337', '0.303', '-0.6147', '0.4585', '-0.5957', '-0.163', '0.2368', '0.6465', '-0.1156', '0.2292', '0.05078', '0.04446', '-0.2598', '0.4163', '0.2974', '0.2783', '-0.1687', '-0.01226', '-0.3762', '-0.362', '-0.03937', '-0.3127', '-0.772', '0.1721', '0.4707', '0.02274', '-0.02069', '-0.4045', '-0.0819', '0.0822', '0.364', '0.002947', '-0.5386', '0.647', '-0.2734', '-0.06744', '0.4077', '-0.1951', '0.065', '0.1692', '-0.1055', '-0.4663', '-0.4128', '-0.1414', '-0.1381', '-0.01502', '-0.3057', '-0.3533', '0.0433', '0.4443', '0.4978', '-0.1681', '0.8984', '-0.7026', '0.4417', '0.228', '-0.0788', '-0.383', '0.3643', '0.8916', '-0.12036', '-0.5024', '0.4597', '0.4753']",,,C538655,,,,
mondo:0009288,glycogen storage disease Ib,"['glycogen storage disease Ic', 'GSD1C', 'glycogenosis due to glucose-6-phosphatase transport defect type IB', 'glycogen storage disease type IB', 'G6P deficiency type IB', 'GSD Ic', 'G6P translocase deficiency', 'GSD type IB', 'GSD type 1 non a', 'glycogenosis type IB', 'GSD due to G6PT deficiency', 'GSD Ib', 'glycogenosis due to glucose-6-phosphatase deficiency type 1B', 'GSD type 1b', 'glycogen storage disease type Ic', 'Gsd1C', 'glycogen storage disease Ib', 'glycogen storage disease type 1b', 'glycogen storage disease due to G6P deficiency type IB', 'glucose-6-phosphate transport defect', 'G6PT deficiency', 'GSD1B', 'GSD due to G6P deficiency type IB', 'glycogenosis type 1b', 'GSDIb', 'glycogen storage disease type I non-a']",0081331,232240,79259,C0342749,"['-0.1632', '0.01999', '-0.036', '0.1715', '0.632', '0.11554', '0.2776', '0.5293', '-0.145', '0.147', '0.161', '-0.1702', '-0.2905', '0.4375', '-0.1898', '-0.05835', '0.05698', '0.01987', '-0.3877', '-0.6025', '0.263', '-0.3623', '0.9546', '-0.3494', '-0.7695', '-0.0748', '-0.012436', '-0.08746', '0.1768', '-0.00694', '0.3982', '0.5684', '0.252', '0.4236', '0.257', '-0.5474', '-0.521', '-0.015205', '-0.1947', '-0.107', '-0.4258', '-0.1791', '0.1805', '0.149', '-0.5215', '0.1768', '0.0669', '0.1874', '0.26', '0.519', '0.2678', '-0.4678', '0.7593', '-0.69', '-0.4702', '-0.3904', '0.697', '-0.2915', '-0.9287', '-0.2019', '0.0239', '0.05014', '0.341', '0.01231', '0.2354', '0.3442', '0.2289', '-0.4587', '-0.671', '-0.0596', '-0.352', '-0.6953', '-0.1272', '-0.2114', '0.5464', '0.000948', '0.1672', '-0.0362', '-0.4634', '-0.1147', '-0.4253', '-0.3828', '-0.161', '-0.2334', '-0.3232', '0.0946', '0.806', '0.29', '0.4902', '-0.4265', '0.4868', '0.1511', '-0.10913', '0.0772', '0.6836', '0.795', '-0.09143', '-0.408', '0.01358', '0.11676']",C122661,,C562594,,,,
mondo:0009290,glycogen storage disease II,"['deficiency of maltase', 'GSD II', 'deficiency of glucoamylase', 'acid maltase deficiency', 'generalised glycogenosis', 'glycogen storage disease II', 'Cardiomegalia Glycogenica diffusa', 'glycogen storage disease type II', 'glycogen storage disease type 2', 'GAA glycogen storage disease', 'glycogenosis, type 2', 'glycogenosis due to acid maltase deficiency', 'glycogen storage disease caused by mutation in GAA', 'Alpha-1,4-glucosidase acid deficiency', 'lysosomal alpha-1,4-glucosidase deficiency', 'GSD 2', 'GSD type II', 'acid maltase deficiency disease', 'deficiency of alpha-glucosidase', 'glycogen storage disease, type II', 'glycogenosis, generalized, Cardiac form', 'glycogen storage disease due to acid maltase deficiency', 'deficiency of lysosomal alpha-glucosidase', 'GSD2', 'glycogenosis type 2', 'generalized glycogenosis', 'glucosidase acid-1,4-alpha deficiency', 'Aglucosidase alfa', 'glycogen storage disease 2', 'Pompe disease', 'GSD due to acid maltase deficiency', 'Pompe^s disease', 'glycogenosis type II', 'GSD type 2', 'Alpha-1,4-glucosidase deficiency', 'GAA deficiency']",2752,232300,365,C1968741,"['-0.3564', '0.4224', '0.3962', '-0.1498', '0.3088', '-0.739', '0.2179', '0.3625', '-0.606', '0.1282', '-0.5034', '0.1', '-0.3872', '0.0856', '0.05957', '-0.0948', '-0.8057', '-0.0835', '-0.8555', '-0.767', '0.1279', '-0.25', '0.8975', '-0.2727', '-0.484', '-0.3542', '0.3967', '0.006126', '0.05173', '-0.004986', '0.2114', '0.1742', '0.4675', '0.2417', '-0.05072', '-0.1903', '-0.555', '0.449', '-0.0562', '0.1959', '-0.3909', '-0.625', '0.4915', '0.4502', '-0.3975', '-0.08514', '0.01775', '0.02217', '-0.1039', '0.5356', '-0.11694', '0.136', '0.1711', '-0.254', '-0.05634', '-1.039', '0.0426', '0.08276', '0.02875', '-0.1059', '0.2761', '-0.1344', '0.1943', '0.14', '-0.10455', '-0.06573', '0.551', '0.2354', '-0.3215', '-0.279', '0.07184', '0.123', '0.144', '0.2274', '0.3542', '0.2595', '0.1881', '0.1278', '-0.4004', '0.11383', '-0.031', '-0.07477', '-0.1615', '0.2008', '0.3252', '0.2822', '0.3313', '-0.2079', '0.54', '-0.2815', '0.4023', '0.2847', '0.0191', '-0.2493', '0.5283', '0.8853', '0.3706', '-0.1096', '-0.061', '-0.0386']",C84734,,,,,10053185,
mondo:0009291,glycogen storage disease III,"['glycogen storage disease III', 'glycogen storage disease type III', 'glycogenosis due to glycogen debranching enzyme deficiency', 'GDE deficiency', 'Cori disease', 'Agl deficiency', 'deficiency of dextrin', 'glycogen storage disease IIID', 'GSD type 3', 'GSDIII', 'glycogen storage disease 3', 'amylo-1,6-glucosidase deficiency', 'glycogen storage disease IIIC', 'glycogenosis type III', 'Cori-Forbes disease', 'Gde deficiency', 'glycogen storage disease, type III', 'glycogen storage disease caused by mutation in AGL', 'amylo 1,6 glucosidase deficiency', 'GSD due to glycogen debranching enzyme deficiency', 'AGL glycogen storage disease', 'glycogenosis type 3', 'glycogen Debrancher deficiency', 'deficiency of debranching enzyme', 'GSD3', 'glycogen storage disease due to glycogen debranching enzyme deficiency', 'glycogen storage disease IIIa', 'glycogen storage disease type 3', 'glycogen storage disease IIIb', 'limit dextrinosis', 'Forbes disease']",2748,232400,366,CN204781,"['0.1958', '0.08386', '-0.5273', '-0.3218', '0.497', '-0.6987', '0.0309', '0.751', '-0.27', '0.0788', '-0.1066', '-0.1614', '0.0864', '0.2637', '-0.5674', '0.1611', '-0.1442', '-0.6094', '-0.674', '-0.1364', '0.1461', '-0.549', '0.7837', '0.3914', '-0.5723', '-0.07043', '-0.2002', '-0.3748', '-0.4922', '0.0571', '0.5728', '-0.0764', '0.399', '0.4536', '-0.4453', '-0.2913', '-0.584', '-0.056', '-0.0229', '0.05814', '-0.2666', '-0.2499', '0.01878', '0.838', '-0.303', '0.2375', '0.224', '0.053', '-0.484', '0.8403', '-0.3367', '0.02081', '0.2512', '-0.08276', '0.01537', '-0.4998', '0.2474', '-0.2217', '-0.31', '0.251', '0.5093', '0.0181', '0.679', '-0.1065', '-0.6665', '0.36', '0.3271', '0.0965', '-0.3357', '0.371', '-0.5137', '-0.0183', '0.1979', '0.158', '0.793', '0.0476', '-0.04333', '-0.3518', '-0.587', '0.1727', '0.142', '-0.452', '-0.5093', '-0.2273', '0.0916', '0.3918', '0.2534', '0.01389', '0.7324', '-0.1057', '0.403', '-0.2336', '-0.2', '-0.0342', '0.2832', '0.3118', '0.2407', '-0.2964', '-0.0809', '0.1169']",C84736,,D006010,,,10053250,
mondo:0009292,glycogen storage disease due to glycogen branching enzyme deficiency,"['glycogen storage disease 4', 'GSD due to glycogen branching enzyme deficiency', 'glycogen storage disease caused by mutation in GBE1', 'glycogenosis type 4', 'GSD IV, classic hepatic', 'GSD IV, neuromuscular form, adult, with isolated myopathy', 'GSD 4', 'GSD type 4', 'branching-transferase deficiency glycogenosis', 'brancher deficiency', 'brancher deficiency glycogenosis', 'GSD IV, nonprogressive hepatic', 'glycogenosis due to glycogen branching enzyme deficiency', 'glycogenosis type IV', 'GSD IV, neuromuscular form, congenital', 'cirrhosis, familial, with deposition of abnormal glycogen', 'glycogen storage disease type IV', 'GSD type IV', 'GSD IV, neuromuscular form, fatal perinatal', 'Gbe1 deficiency', 'glycogen storage disease IV', 'GBE1 glycogen storage disease', 'glycogen storage disease, type IV', 'amylopectinosis', 'GSD IV, neuromuscular form, childhood', 'glycogen branching enzyme deficiency', 'Andersen disease', 'deficiency of 1,4-alpha-glucan branching enzyme', 'GSD4', 'glycogenosis 4', 'GSD IV', 'glycogen storage disease type 4']",2750,232500,367,CN204783,"['-0.11145', '0.08417', '0.124', '0.003284', '0.19', '-0.566', '0.0639', '0.452', '-0.3962', '-0.387', '-0.02486', '-0.299', '-0.2625', '0.4346', '-0.01468', '-0.5903', '-0.4814', '-0.412', '-0.306', '-0.6377', '0.2408', '-0.3638', '0.893', '-0.6416', '-0.4128', '-0.07117', '0.07306', '0.3716', '-0.2878', '0.389', '0.574', '0.3367', '0.522', '0.02037', '0.0785', '-0.4863', '-0.692', '0.3577', '-0.224', '0.5166', '-0.0835', '-0.535', '-0.12006', '0.0788', '-0.659', '0.3672', '0.03558', '0.06885', '-0.2112', '0.608', '-0.0479', '0.1803', '0.1919', '-0.1643', '-0.365', '-1.0', '-0.1337', '-0.3027', '-0.2372', '0.1652', '-0.0717', '-0.01819', '0.1486', '-0.1613', '-0.302', '-0.0492', '0.523', '0.3813', '-0.5566', '-0.2239', '-0.0998', '0.0315', '0.4343', '0.0773', '0.4202', '0.1212', '-0.2212', '-0.1653', '-0.7197', '0.3535', '-0.3718', '-0.3418', '0.0605', '0.0996', '0.2896', '-0.126', '0.4995', '-0.1365', '0.2247', '0.0647', '0.7646', '0.128', '0.1447', '0.1588', '0.481', '0.517', '0.253', '-0.09784', '0.1633', '-0.2196']",C84737,,,277.6,,10053249,
mondo:0009293,glycogen storage disease V,"['McArdle^s disease', 'GSD 5', 'glycogen storage disease caused by mutation in PYGM', 'glycogen storage disease type 5', 'Pygm deficiency', 'glycogenosis type V', 'glycogen storage disease 5', 'glycogenosis type 5', 'McArdle type glycogen storage disease', 'GSD due to muscle glycogen phosphorylase deficiency', 'GSD type V', 'PYGM glycogen storage disease', 'glycogen storage disease type V', 'glycogenosis due to muscle glycogen phosphorylase deficiency', 'McArdle disease', 'glycogen storage disease V', 'GSD5', 'glycogen storage disease, type V', 'muscle glycogen phosphorylase deficiency', 'GSD type 5', 'glycogen storage disease due to muscle glycogen phosphorylase deficiency', 'Mcardle disease', 'myophosphorylase deficiency']",2746,232600,368,C0017924,"['-0.176', '0.1924', '-0.4045', '0.0836', '0.0004146', '-0.68', '0.0723', '0.829', '-0.3674', '0.3271', '-0.155', '0.6094', '0.10315', '-0.0571', '-0.2128', '-0.006905', '-0.3628', '-0.2261', '-0.11816', '-0.54', '0.2325', '-0.5415', '0.426', '0.11755', '-0.4114', '-0.2456', '-0.1362', '-0.402', '-0.577', '-0.0897', '0.3035', '0.075', '0.48', '0.04724', '0.02301', '-0.624', '-0.129', '0.556', '-0.00782', '0.06042', '-0.1594', '-0.7935', '0.4797', '0.158', '-0.4001', '0.3442', '-0.4495', '0.0838', '-0.086', '0.722', '-0.11395', '-0.0493', '0.473', '-0.256', '-0.2861', '-0.709', '0.2598', '-0.3682', '0.3262', '-0.1926', '0.2695', '0.0594', '0.095', '-0.7476', '-0.2327', '0.405', '0.2241', '0.4531', '-0.5103', '0.1162', '0.214', '-0.1075', '0.2203', '0.1399', '0.441', '0.7153', '-0.2047', '-0.2756', '-0.439', '0.1428', '0.4573', '-0.528', '-0.008095', '-0.1705', '0.77', '0.5234', '0.10333', '0.1487', '0.958', '0.247', '0.62', '0.169', '-0.1628', '0.0453', '0.7334', '0.4893', '-0.09625', '0.0823', '-0.1327', '-0.2903']",C84738,,D006012,,,10018462,
mondo:0009294,glycogen storage disease VI,"['PYGL glycogen storage disease', 'hepatic glycogen phosphorylase deficiency', 'GSD type VI', 'hepatophosphorylase deficiency glycogenosis', 'glycogen storage disease type VI', 'glycogen storage disease due to liver glycogen phosphorylase deficiency', 'liver glycogen phosphorylase deficiency', 'GSD6', 'glycogen storage disease type 6', 'glycogenosis due to liver glycogen phosphorylase deficiency', 'hers disease', 'hers^ disease', 'GSD due to liver glycogen phosphorylase deficiency', 'glycogen storage disease VI', 'phosphorylase deficiency glycogen-storage disease of liver', 'hepatic phosphorylase deficiency', 'glycogenosis type VI', 'GSD type 6', 'GSD 6', 'glycogenosis type 6', 'glycogen storage disease 6', 'glycogen storage disease caused by mutation in PYGL']",2754,232700,369,C0017925,"['-0.144', '0.1667', '-0.1381', '-0.05505', '0.264', '-0.5225', '0.003178', '0.5635', '-0.2207', '0.0728', '-0.4844', '0.3745', '0.162', '-0.01062', '-0.02692', '0.04413', '0.0447', '-0.2913', '-0.6357', '-0.665', '0.11725', '-0.7046', '0.4727', '0.3374', '-0.185', '-0.2603', '-0.02962', '-0.1752', '-0.05267', '-0.0937', '0.447', '0.385', '0.1578', '0.2903', '-0.2244', '-0.2925', '-0.3237', '0.1337', '0.02754', '-0.01912', '-0.1727', '-0.05914', '0.2524', '0.615', '-0.476', '0.05106', '-0.088', '-0.0719', '0.1305', '0.4434', '-0.1473', '0.0413', '0.04636', '0.10016', '-0.1726', '-0.5864', '0.1901', '-0.139', '-0.3457', '0.3042', '0.3257', '0.2021', '0.3677', '-0.606', '0.0435', '0.1447', '0.208', '0.0874', '-0.363', '-0.01639', '-0.04755', '0.0721', '0.0353', '0.187', '0.3982', '0.2051', '0.0355', '0.1434', '-0.3792', '0.1625', '-0.1415', '-0.003275', '-0.2783', '-0.325', '0.1814', '0.2837', '0.298', '-0.428', '0.846', '0.4246', '0.386', '0.3833', '-0.316', '-0.2211', '0.557', '0.323', '0.2433', '-0.4373', '0.01933', '-0.03372']",C126875,,D006013,,,10053240,
mondo:0009295,glycogen storage disease VII,"['GSDVII', 'GSD type VII', 'Pfkm deficiency', 'glycogen storage disease due to muscle phosphofructokinase deficiency', 'glycogen storage disease caused by mutation in PFKM', 'glycogen storage disease type 7', 'glycogen storage disease 7', 'glycogen storage disease VII', 'PFKM glycogen storage disease', 'glycogenosis due to muscle phosphofructokinase deficiency', 'GSD due to muscle phosphofructokinase deficiency', 'glycogen storage disease type VII', 'glycogenosis type VII', 'glycogen storage disease, type VII', 'GSD type 7', 'muscle phosphofructokinase deficiency', 'Tarui disease', 'phosphofructokinase deficiency', 'glycogenosis type 7', 'GSD 7', 'GSD7', 'phosphofructokinase myopathy']",11721,232800,371,C0017926,"['-0.34', '0.4788', '-0.4854', '-0.2727', '0.3237', '-0.706', '-0.6025', '0.9526', '0.1869', '-0.0781', '0.2773', '-0.1156', '-0.0973', '0.3245', '-0.06354', '-0.3704', '-0.431', '-0.1987', '-0.3882', '-0.2489', '0.4946', '-0.4248', '0.3008', '0.1462', '-0.4136', '0.1808', '0.2069', '-0.4048', '-0.1382', '-0.0856', '-0.1096', '0.1606', '0.3057', '0.0795', '-0.535', '-0.4534', '-0.7383', '-0.289', '-0.1486', '0.096', '0.06384', '-0.751', '-0.001487', '0.144', '-0.3816', '0.3938', '0.08875', '-0.1047', '0.0988', '0.2505', '-0.2336', '-0.428', '0.2808', '0.00479', '-0.1938', '-0.387', '0.4424', '0.10876', '-0.1686', '0.0449', '0.3591', '0.1371', '0.2292', '-0.6753', '-0.4165', '0.0978', '0.3884', '0.06323', '-0.4255', '-0.1128', '-0.1984', '-0.2747', '-0.1278', '0.03732', '0.7466', '0.579', '-0.4597', '0.1846', '-0.1295', '0.05792', '0.221', '-0.2942', '0.01013', '-0.2162', '0.5596', '0.605', '0.1842', '0.317', '0.8115', '-0.1215', '0.392', '-0.281', '0.1135', '-0.00938', '0.62', '0.859', '0.00823', '-0.38', '-0.3628', '-0.0489']",C118437,,D006014,,,10053241,
mondo:0009296,glycoprotein storage disease,['glycoprotein storage disease'],,232900,,C1856275,,,,C565538,,,,
mondo:0009297,familial renal glucosuria,"['renal glucosuria', 'renal diabetes', 'SGLT2 deficiency', 'Glys1', 'GLYS', 'familial renal glucosuria', 'glycosuria, renal', 'renal glycosuria']",9432,233100,69076,C3245525,"['-0.5596', '-0.226', '0.2108', '-0.254', '0.05435', '-0.5493', '-0.1294', '1.15', '0.02359', '-0.03096', '-0.541', '-0.2012', '-0.04694', '0.3696', '-0.2466', '0.003323', '0.2527', '0.1658', '-0.134', '-0.5205', '0.03378', '-0.1952', '0.1733', '-0.3857', '0.2534', '0.045', '0.11505', '-0.1061', '0.1555', '-0.00083', '0.3652', '-0.2678', '0.2498', '-0.02777', '-0.2905', '0.11957', '-0.3088', '0.0922', '-0.2148', '0.2113', '-0.3142', '0.1954', '0.4436', '-0.2717', '-0.2163', '-0.2747', '-0.275', '-0.1853', '-0.11414', '0.4604', '-0.2051', '0.03574', '-0.0688', '-0.12213', '0.11194', '-0.053', '0.465', '-0.508', '-0.4482', '0.5674', '0.5405', '0.1537', '0.6465', '-0.2808', '0.1442', '-0.2815', '0.196', '0.1106', '-0.202', '0.2983', '0.1343', '-0.3066', '-0.1148', '0.35', '0.08704', '0.3472', '0.3076', '-0.1508', '-0.332', '0.208', '0.05624', '0.3853', '0.6255', '-0.4055', '-0.04053', '0.388', '0.3235', '0.0662', '0.424', '0.04163', '0.486', '0.5015', '-0.1162', '-0.167', '0.4634', '0.3655', '0.8467', '-0.8857', '-0.0749', '0.1879']",,1001151,D006030,271.4,,10038457,
mondo:0009298,GOMBO syndrome,"['Growth retardation, ocular abnormalities, microcephaly, brachydactyly, and oligophrenia', 'GOMBO syndrome']",,233270,,C1856274,,,,C537284,,,,
mondo:0009299,46 XX gonadal dysgenesis,"['46,XX complete gonadal dysgenesis', 'XX female gonadal dysgenesis', '46,XX pure gonadal dysgenesis', 'XX gonadal dysgenesis', 'XX-GD', 'hypergonadotropic ovarian dysgenesis', 'ovarian dysgenesis', 'follicular stimulating hormone-resistant ovaries', '46,XX ovarian dysgenesis', 'FSH-RO', '46,XX gonadal dysgenesis']",14450,,243,C0949595,"['-0.0496', '0.0151', '-0.2343', '-0.1737', '0.0333', '-0.2445', '-0.513', '0.5244', '-0.1716', '-0.5957', '0.3948', '-0.666', '-0.6113', '0.5566', '0.5015', '-0.5693', '0.3613', '-0.00622', '0.0843', '-0.921', '-0.1525', '-0.789', '0.7856', '-0.6885', '0.4646', '0.4326', '-0.02022', '-0.2983', '0.6313', '-0.2479', '0.8223', '-0.0004501', '0.3618', '-0.485', '-0.6836', '-0.3684', '0.2399', '-0.548', '-0.3203', '-0.2832', '0.7495', '0.1976', '0.4575', '0.147', '0.1321', '-0.492', '-0.0718', '-0.2559', '0.1274', '0.5015', '0.363', '-0.5947', '-0.04498', '-0.2089', '-0.4504', '-0.1722', '0.7305', '-0.8525', '-0.3367', '1.029', '0.2542', '0.335', '0.1786', '0.162', '-0.1937', '-0.098', '0.4902', '-0.001208', '-0.4558', '0.2517', '-0.1404', '0.2703', '0.3687', '-0.295', '0.09973', '-0.1454', '0.4824', '0.2169', '-0.2898', '0.10913', '-0.03513', '0.7744', '0.1613', '-0.1959', '-0.256', '-0.3425', '0.271', '-0.2917', '0.516', '0.5034', '0.2286', '0.5586', '-0.5166', '-0.07855', '0.516', '-0.28', '0.1675', '0.4949', '0.05594', '-0.07605']",C120197,,D023961,,,,
mondo:0009300,Perrault syndrome 1,"['PRLTS1', 'HSD17B4 Perrault syndrome', 'Perrault syndrome 1', 'Perrault syndrome caused by mutation in HSD17B4', 'ovarian dysgenesis with sensorineural deafness', 'Perrault syndrome type 1', 'gonadal dysgenesis, 20 type, with deafness']",,233400,642945,,,,,,,,,
mondo:0009301,"46,XY sex reversal 7","['46,XY gonadal dysgenesis, partial or complete, Dhh-related', '46,XY sex reversal 7', '46,XY SEX reversal 7', 'SRXY7', 'gonadal dysgenesis, XY, Male-limited', '46XY sex reversal 7', '46,XY Sex reversal, partial or complete, Dhh-related', '46,XY Sex reversal type 7']",0111774,233420,,,,,,C565537,,,,
mondo:0009302,XY type gonadal dysgenesis-associated anomalies syndrome,"['gonadal dysgenesis, XY type, with associated anomalies', 'gonadal dysgenesis, 10Y type, with associated anomalies', 'gonadal dysgenesis XY type associated anomalies']",,233430,1770,C1856272,,,,C565536,,,,
mondo:0009303,anti-glomerular basement membrane disease,"['glomerulonephritis - pulmonary haemorrhage', 'anti-glomerular basement membrane disease', 'pulmonary renal syndrome', 'anti-glomerular basement membrane antibody disease', 'rapidly progressive glomerulonephritis with pulmonary hemorrhage', 'rapidly progressive glomerulonephritis with pulmonary haemorrhage', 'Goodpasture syndrome', 'anti-GBM syndrome', 'glomerulonephritis - pulmonary hemorrhage']",9808,233450,375,C0403529,,C84566,0007290,D019867,446.21,,10018620,
mondo:0009305,granulocytopenia with immunoglobulin abnormality,"['immunodeficiency 59 and hypoglycemia', 'granulocytopenia with immunoglobulin abnormality']",0111974,233600,,C1856263,"['0.001808', '0.01923', '0.008385', '-0.0123', '0.004784', '-0.006184', '0.002104', '0.003027', '-0.0114', '-0.00917', '-0.001553', '-0.00602', '-0.0049', '0.01505', '-0.01387', '-0.00758', '0.00952', '-0.001273', '-0.00835', '-0.02847', '0.004856', '-0.01147', '0.007996', '0.003508', '0.001295', '0.003326', '0.007835', '0.002169', '0.007782', '-0.01181', '0.0097', '-0.006737', '0.010124', '-0.002016', '-0.003178', '-0.005127', '-0.0005827', '-0.00736', '0.004524', '-0.011795', '0.01267', '-0.01897', '0.012985', '-0.011986', '-0.0009136', '-0.00495', '-0.002735', '0.0073', '0.002733', '-0.00209', '-0.00431', '0.0018835', '-0.004196', '-0.001966', '-0.003012', '-0.004055', '0.01826', '-0.001191', '-0.006954', '-0.00315', '0.007393', '0.01113', '-0.00864', '0.01157', '-0.00844', '0.00464', '0.01158', '0.01639', '-0.013626', '0.01121', '-0.00879', '-0.000985', '-0.006187', '0.0004187', '-0.003794', '0.006035', '0.00772', '-0.0067', '-0.01026', '-0.0158', '0.002178', '0.0008245', '0.001602', '0.0118', '-0.0008235', '-0.0014715', '-0.007607', '0.0164', '0.006985', '0.01009', '0.01223', '0.00909', '-0.00972', '0.00593', '0.01505', '0.00636', '0.007217', '-0.01293', '0.0003078', '0.001883']",,,C565535,,,,
mondo:0009306,combined immunodeficiency with skin granulomas,"['combined cellular and humoral immune defects with granulomas', 'CCHIDG', 'combined immunodeficiency due to RAG 1/2 deficiency', 'CID due to RAG 1/2 deficiency']",0112253,233650,157949,C2673536,"['-0.1641', '0.275', '0.2568', '-0.597', '0.01384', '-0.104', '0.197', '-0.2732', '-0.1366', '0.0484', '-0.03918', '0.1815', '-0.1562', '-0.02855', '-0.1383', '0.08124', '0.1065', '0.0787', '-0.33', '-0.513', '-0.06152', '-0.243', '0.549', '-0.1609', '-0.1583', '-0.1511', '-0.1816', '0.0724', '-0.1227', '-0.5664', '0.1698', '0.297', '0.522', '0.1409', '0.373', '0.1251', '-0.3325', '0.1721', '-0.2212', '-0.3381', '0.03903', '-0.1018', '0.03967', '-0.1063', '-0.128', '-0.4084', '-0.1443', '0.04413', '0.02548', '0.2374', '-0.2043', '0.1213', '0.5713', '0.08453', '-0.2117', '0.1542', '0.1473', '-0.3079', '-0.316', '-0.06647', '0.0666', '0.2026', '-0.1997', '0.1666', '0.464', '-0.1738', '0.2864', '0.1918', '-0.03104', '0.452', '-0.1531', '-0.2983', '-0.08026', '-0.05347', '-0.134', '-0.1161', '0.1733', '0.264', '0.06067', '0.0372', '-0.2153', '-0.1556', '-0.04266', '-0.01458', '-0.1771', '-0.1753', '0.1368', '0.2595', '0.2269', '0.03354', '0.3652', '0.2113', '-0.0397', '-0.0936', '0.609', '0.4407', '0.2542', '-0.1576', '0.0653', '0.01246']",,,C567115,,,,
mondo:0009307,granulomatous disease with defect in neutrophil chemotaxis,['granulomatous disease with defect in neutrophil chemotaxis'],,233670,,C1856261,,,,C565534,,,,
mondo:0009308,"granulomatous disease, chronic, autosomal recessive, cytochrome b-negative","['Cyba deficiency', 'chronic granulomatous disease 4, autosomal recessive', 'CGD due to deficiency of the Alpha Subunit of cytochrome B', 'granulomatous disease, chronic, autosomal recessive, cytochrome b-negative', 'CGD, autosomal recessive cytochrome B-negative']",0070193,233690,,C1856255,,,,C565533,,,,
mondo:0009309,"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 1","['granulomatous disease, chronic, due to Ncf1 deficiency', 'CGD, autosomal recessive cytochrome B-positive, type 1', 'CDG1', 'granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type I', 'NCF1 chronic granulomatous disease', 'chronic granulomatous disease caused by mutation in NCF1', 'neutrophil cytosol Factor 1, deficiency of', 'Soc2, deficiency of', 'chronic granulomatous disease 1, autosomal recessive', 'Ncf1, deficiency of', 'p47-PHOX, deficiency of', 'soluble oxidase component II, deficiency of']",0070192,233700,,C1856251,,,,C565532,,,,
mondo:0009310,"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 2","['NCF2 chronic granulomatous disease', 'granulomatous disease, chronic, due to Ncf2 deficiency', 'CDG2', 'CGD, autosomal recessive cytochrome B-positive, type 2', 'Ncf2, deficiency of', 'chronic granulomatous disease caused by mutation in NCF2', 'P67-PHOX, deficiency of', 'chronic granulomatous disease 2, autosomal recessive', 'granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type II', 'neutrophil cytosol Factor 2, deficiency of']",0070191,233710,,C1856245,,,,C565531,,,,
mondo:0009311,grouped pigmentation of the retina,"['grouped pigmentation of retinal pigment epithelium', 'grouped pigmentation of the retina', 'grouped pigmentation of the macula']",,233800,,C1856244,,,,C565530,,,,
mondo:0009312,lipodystrophy due to peptidic growth factors deficiency,"['peptidic growth factors deficiency', 'Werner-like syndrome due to combined growth factor deficiency', 'combined insulin, insulin-like growth factor 1 (IGF1) and epidermal growth factor (EGF) deficiency', 'Hoepffner Dreyer Reimers syndrome', 'growth factors, combined defect OF', 'Hoepffner-Dreyer-Reimers syndrome', 'insulin, insulin-like Growth Factor I, and Epidermal Growth Factor deficiency', 'peptide growth factors deficiency', 'Werner-like syndrome due to combined Growth Factor deficiency']",,233805,1979,C2931279,,,,C565529,,,,
mondo:0009313,Grubben-de Cock-Borghgraef syndrome,"['growth retardation, small and puffy hands and feet, and eczema', 'developmental delay-hypotonia-extremities hypertrophy syndrome', 'severe growth retardation, developmental delay with hypotonia, hypotrophy of the distal extremities, dental anomalies, and eczematous skin', 'developmental delay - hypotonia - extremities hypertrophy', 'Grubben de Cock Borghgraef syndrome']",,233810,2101,C2931551,,,,C537621,,,,
mondo:0009315,congenital factor XII deficiency,"['F12 deficiency', 'factor XII deficiency disease', 'Hageman Factor deficiency', 'congenital Hageman factor deficiency', 'Haf deficiency', 'factor 12 deficiency', 'factor XII deficiency', 'coagulation factor 12 deficiency', 'deficiency, Hageman']",2231,234000,330,C0015526,"['-0.1593', '0.1677', '-0.4656', '0.01855', '-0.1455', '0.11523', '0.12146', '-0.2175', '0.1975', '-0.1567', '0.2389', '0.225', '0.2211', '-0.2864', '-0.2279', '0.056', '0.31', '0.1066', '-0.1683', '-0.883', '0.1573', '0.1062', '0.497', '-0.1508', '-0.03604', '0.09125', '0.337', '-0.1244', '0.03464', '-0.2262', '0.494', '0.309', '0.1656', '0.3809', '-0.5234', '-0.3596', '0.3137', '-0.11694', '-0.1714', '-0.7627', '0.1787', '0.2808', '0.0954', '-0.1449', '-0.1114', '-0.3457', '-0.2281', '-0.0759', '0.332', '0.789', '0.0521', '-0.246', '0.12244', '-0.1194', '-0.6455', '0.0317', '0.1464', '-0.001266', '-1.141', '0.2205', '0.055', '0.2927', '0.7847', '-0.0179', '0.2225', '0.273', '0.01048', '0.001386', '-0.51', '0.4312', '-0.08466', '-0.0403', '-0.0729', '-0.1986', '0.582', '-0.1797', '0.516', '0.344', '0.267', '-0.03323', '-0.732', '-0.2607', '0.03564', '-0.073', '0.05322', '0.09106', '0.00767', '0.5693', '0.387', '-0.324', '0.0968', '0.536', '-0.1669', '-0.366', '0.546', '0.3503', '0.307', '-0.627', '-0.6094', '0.2317']",C131740,,D005175,286.3,,,
mondo:0009318,Hallermann-Streiff syndrome,"['oculomandibulofacial syndrome', 'François dyscephalic syndrome', 'Francois dyscephalic syndrome', 'FranC^ois dyscephalic syndrome', 'Hallermann-Streiff syndrome', 'HSS', 'Hallermann^s syndrome', 'Hallermann Streiff Francois syndrome', 'Hallerman - Streiff syndrome', 'Hallermann Streiff syndrome', 'Hallermann syndrome']",4534,234100,2108,C0018522,"['-0.06204', '-0.09485', '0.6914', '-0.5044', '0.1262', '-0.00859', '0.1854', '0.604', '-0.4287', '-0.231', '-0.3057', '-0.0784', '-0.127', '0.01833', '-0.528', '0.013054', '0.667', '-0.3', '-0.4827', '-0.6074', '-0.1993', '0.03506', '0.10614', '-0.1686', '-0.00977', '-0.0859', '-0.402', '0.0436', '0.3806', '-0.2145', '0.2118', '-0.1301', '0.2927', '-0.01764', '0.3755', '0.1863', '0.084', '-0.3496', '-0.1221', '-0.5884', '0.252', '-0.3389', '-0.09125', '-0.2847', '0.3503', '-0.4028', '0.2456', '0.514', '0.1234', '-0.2915', '-0.1847', '0.3904', '0.0643', '0.1333', '-0.3433', '-0.2642', '0.2388', '-0.1747', '-0.1948', '-0.1453', '0.0206', '-0.1301', '-0.3508', '0.07764', '0.01993', '0.0885', '0.2145', '0.4832', '-0.0846', '0.3228', '-0.502', '0.3857', '0.325', '-0.0673', '-0.12244', '-0.12354', '0.3152', '-0.5337', '-0.03004', '-0.11694', '0.07935', '0.0699', '-0.00753', '0.2905', '-0.1333', '-0.167', '0.006535', '0.1865', '0.2927', '0.0924', '-0.01049', '0.5283', '0.2932', '0.1555', '0.5005', '0.08746', '0.3542', '-0.1979', '0.522', '0.07324']",C84746,,D006210,,,,
mondo:0009319,pantothenate kinase-associated neurodegeneration,"['neurodegeneration with brain iron accumulation type 1', 'NBIA1', 'PKAN', 'neurodegeneration with brain iron accumulation 1', 'Hallervorden-Spatz syndrome', 'pigmentary pallidal degeneration', 'brain iron accumulation type I syndrome', 'neuroaxonal dystrophy, late infantile', 'Hallervorden-Spatz disease', 'Pkan neuroaxonal dystrophy, juvenile-onset', 'pantothenate kinase-associated neurodegeneration']",3981,234200,157850,C0018523,"['0.4268', '0.508', '-0.1027', '-0.295', '0.05475', '-0.4673', '-0.068', '0.812', '-0.3525', '0.4048', '-0.6035', '-0.0909', '0.3787', '0.2998', '-0.006157', '-0.822', '-0.0957', '-0.45', '-0.0841', '-0.8574', '-0.1455', '-0.7925', '-0.03714', '0.1989', '-0.3928', '-0.1604', '0.1277', '-0.766', '-0.601', '0.2676', '0.2084', '-0.07837', '-0.05994', '-0.1053', '0.1624', '-0.08856', '-0.3435', '-0.3096', '-0.0666', '0.1892', '0.3445', '-0.3582', '-0.1406', '0.3425', '0.5967', '0.5483', '-0.1692', '-0.3281', '-0.874', '0.4446', '0.2886', '0.6523', '-0.628', '-0.4578', '-0.07983', '0.1919', '0.01509', '0.2744', '-0.1445', '-0.1004', '0.472', '0.08344', '0.04938', '-0.4832', '-0.3435', '-0.002647', '0.784', '0.3005', '-0.554', '0.2974', '-0.0765', '-0.151', '-0.256', '-0.6655', '0.4443', '-0.0606', '-0.00907', '-0.0378', '-0.4348', '-0.355', '0.2368', '-1.041', '0.03693', '0.908', '0.2059', '0.2122', '-0.2708', '-0.04227', '0.3838', '-0.206', '0.4006', '0.6934', '0.1044', '0.7324', '0.283', '0.4468', '-0.04752', '0.4644', '-0.10645', '0.1694']",C84988,,D006211,333.0,,,
mondo:0009320,Hall-Riggs syndrome,"['HALL-Riggs intellectual disability syndrome', 'Hall Riggs intellectual disability syndrome', 'HALL-Riggs mental retardation syndrome', 'Hall Riggs mental retardation syndrome']",,234250,2107,C1856198,,,,C535623,,,,
mondo:0009321,hallux varus-preaxial polysyndactyly syndrome,"['hallux varus and preaxial polysyndactyly', 'Kleiner-Holmes syndrome', 'Kleiner Holmes syndrome']",,234280,2110,C1856197,,,,C536885,,,,
mondo:0009323,Halothane hepatitis,['Halothane hepatitis'],,234350,,C0241913,,,,C562477,,,,
mondo:0009324,Hartnup disease,"['Hartnup disease', 'neutral amino acid transport defect', 'deficiency of tryptophan oxygenase', 'HND', 'aminoaciduria, Hartnup type', 'Hartnup disorder']",1060,234500,2116,C0018609,"['0.33', '0.3403', '-0.3557', '-0.2433', '-0.05582', '0.05847', '-0.4167', '0.3284', '0.2251', '-0.1604', '-0.1792', '-0.005955', '0.288', '0.3257', '-0.0427', '0.414', '0.4443', '-0.2336', '-0.623', '-0.4382', '0.04608', '-0.3413', '0.2195', '-0.166', '-0.4841', '-1.057', '0.02835', '-0.11163', '0.02185', '-0.1605', '0.487', '0.05328', '0.424', '-0.0281', '-0.3345', '0.2222', '-0.486', '-0.2913', '-0.1759', '0.6353', '0.633', '-0.325', '0.8306', '-0.0797', '-0.4106', '-0.797', '0.1831', '0.06198', '0.243', '0.527', '-0.345', '0.1093', '-0.5854', '-0.2659', '0.1089', '-0.4604', '0.7534', '-0.07635', '-0.5444', '0.1559', '0.3', '0.337', '0.2136', '0.3276', '-0.3242', '0.012344', '1.139', '-0.00624', '0.1282', '0.4487', '-0.6094', '-0.1304', '-0.05478', '0.4395', '0.2448', '0.5894', '0.2783', '-0.8784', '0.3052', '-0.1597', '0.2388', '-0.947', '0.3218', '0.03375', '0.671', '0.6045', '0.1705', '-0.000514', '0.2', '0.4412', '0.3257', '0.743', '-0.1111', '-0.3464', '0.02455', '0.5254', '0.1766', '-0.3252', '0.1371', '0.285']",C84748,,D006250,,,10019165,
mondo:0009326,congenital heart block,"['heart block, congenital', 'congenital atrioventricular block']",990,234700,60041,C0149530,,,,C535758,746.86,Q24.6,10019263,
mondo:0009327,"heart, malformation of","['heart, malformation of']",,234750,,,,,,,,,,
mondo:0009328,"hemangiomatosis, cutaneous, with associated features","['hemangiomatosis, cutaneous, with associated features']",,234800,,C0220738,,,,C562438,,,,
mondo:0009329,pulmonary venoocclusive disease 2,"['PVOD2', 'pulmonary capillary hemangiomatosis', 'pulmonary venoocclusive disease 2, autosomal recessive', 'hemangiomatosis, familial pulmonary capillary', 'familial pulmonary capillary hemangiomatosis']",0081269,234810,199241,C0340548,"['-0.2275', '-0.02704', '0.002453', '-0.2505', '0.0348', '-0.3303', '0.1696', '-0.004154', '-0.1782', '0.02223', '-0.1871', '-0.332', '-0.2172', '-0.2136', '-0.2079', '-0.5034', '-0.0983', '0.03102', '0.1548', '-0.5347', '0.077', '-0.0665', '0.442', '-0.2476', '0.0146', '0.1981', '0.1617', '0.345', '0.2432', '-0.12256', '0.4712', '0.1523', '0.3726', '0.02376', '0.01211', '-0.10956', '0.003645', '0.1506', '0.1106', '-0.4983', '0.06433', '-0.315', '0.4111', '-0.02347', '-0.1687', '0.0358', '-0.1193', '0.2155', '-0.0268', '-0.05875', '0.148', '0.1659', '0.4163', '0.0531', '-0.4407', '-0.3293', '0.0556', '-0.06696', '-0.393', '-0.01382', '0.00254', '0.1669', '0.096', '-0.2937', '0.2142', '-0.3328', '0.3506', '0.2067', '-0.4343', '0.4292', '-0.4016', '-0.05145', '0.2703', '0.1663', '-0.156', '-0.1758', '-0.01845', '-0.0188', '-0.1696', '-0.1493', '-0.2394', '0.07745', '-0.02927', '0.05783', '-0.0627', '-0.1716', '0.4136', '0.03506', '-0.06125', '-0.199', '0.11896', '-0.01912', '-0.1609', '0.0369', '0.6543', '0.1897', '0.6406', '-0.3247', '-0.2698', '0.1595']",,,C535861,416.8,,,
mondo:0009330,"hemangiopericytoma, malignant","['malignant hemangiopericytoma', 'hemangiopericytoma, malignant']",,234820,,C0334542,,C4301,,C562740,,,,
mondo:0009331,isolated hemihyperplasia,"['isolated hemihypertrophy', 'IH', 'hemihypertrophy', 'hemi 3 syndrome', 'hemihypertrophy, isolated', 'hemihyperplasia, isolated', 'hemi-3 syndrome', 'hemihyperplasia', 'Hemicorporal hypertrophy']",,235000,2128,C1856184,,,,C565524,,,10019463,
mondo:0009332,congenital hematological disorder,"['congenital hematological system disease', 'congenital hematological disorder', 'congenital haematological system disease']",,,,,,C104003,,,,,,
mondo:0009333,mullerian derivatives-lymphangiectasia-polydactyly syndrome,"['Müllerian derivatives-lymphangiectasia-polydactyly syndrome', 'Urioste syndrome', 'persistence of mullerian derivatives with lymphangiectasia and postaxial polydactyly', 'MULLERIAN derivatives, persistence of, with lymphangiectasia and postaxial polydactyly', 'renal and craniofacial anomalies with persistence of mullerian derivatives, lymphangiectasis, hepatic failure, postaxial polydactyly']",,235255,1655,C1856159,,,,C536478,,,,
mondo:0009334,hemolytic anemia with thermal sensitivity of red cells,['hemolytic anemia with thermal sensitivity of red cells'],,235370,,C1856158,,,,C565522,,,,
mondo:0009335,"hemolytic uremic syndrome, atypical, susceptibility to, 1","['AHUS1', 'hemolytic uremic syndrome, atypical, susceptibility to, type 1', 'hemolytic uremic syndrome, typical', 'susceptibility to atypical hemolytic uremic syndrome 1', 'hemolytic uremic syndrome, atypical, susceptibility to', 'hemolytic uremic syndrome, atypical, susceptibility to, 1', 'Ahus, susceptibility to, 1']",,235400,,,"['-0.06244', '0.1046', '-0.0008354', '-0.04587', '0.0893', '-0.149', '-0.001114', '0.064', '-0.01069', '-0.0663', '0.02666', '0.00936', '0.04428', '-0.02278', '-0.03857', '-0.0885', '-0.04892', '-0.0641', '-0.01309', '-0.2019', '0.05045', '-0.07513', '0.1317', '-0.05023', '0.02095', '-0.03708', '-0.0212', '-0.03226', '-0.02762', '-0.0998', '0.1029', '-0.02472', '0.1688', '0.07745', '0.01735', '-0.08', '-0.10785', '-0.06775', '-0.0587', '-0.0843', '0.003994', '-0.10706', '0.0528', '-0.0659', '-0.02696', '-0.12366', '-0.03918', '0.0658', '0.02777', '0.0539', '-0.03568', '-0.005756', '0.0715', '0.001075', '-0.05566', '-0.02869', '0.08844', '-0.0981', '-0.135', '0.0721', '0.08685', '0.053', '0.03683', '0.03046', '0.0327', '0.05136', '0.1484', '0.1041', '-0.0935', '0.2028', '-0.05176', '-0.04504', '-0.00602', '-0.07965', '0.06885', '0.0675', '0.01406', '-0.018', '-0.00918', '-0.06683', '-0.01548', '-0.01817', '-0.01895', '0.096', '-0.0492', '-0.001073', '0.0828', '0.1058', '0.139', '-0.0462', '0.1332', '0.0813', '0.03925', '-0.06506', '0.2396', '0.1561', '0.1305', '-0.1531', '-0.0471', '0.0231']",,,,,,,
mondo:0009336,"hemosiderosis, pulmonary, with deficiency of gamma-a globulin","['hemosiderosis, pulmonary, with deficiency of gamma-a globulin']",,235500,,,,,,,,,,
mondo:0009337,Hennekam lymphangiectasia-lymphedema syndrome 1,"['lymphatic dysplasia, generalized', 'lymphatic dysplasia, generalised', 'Hennekam lymphangiectasia-lymphedema syndrome type 1', 'HKLLS1', 'Hennekam lymphangiectasia-lymphedema syndrome 1', 'Hennekam syndrome caused by mutation in CCBE1', 'CCBE1 Hennekam syndrome', 'Hennekam lymphangiectasia-lymphedema syndrome']",,235510,,C4012050,,,,,,,,
mondo:0009338,hepatic veno-occlusive disease-immunodeficiency syndrome,"['VODI', 'veno-occlusive disease and immunodeficiency syndrome', 'hepatic venoocclusive disease with immunodeficiency', 'VODI syndrome', 'hepatic veno-occlusive disease with immunodeficiency', 'familial veno-occlusive disease with immunodeficiency']",0112254,235550,79124,C1856128,"['-0.5317', '0.2247', '0.09', '-0.2942', '-0.2844', '-0.01776', '0.04678', '0.0747', '0.00985', '-0.00537', '-0.4763', '-0.2031', '-0.234', '-0.02538', '-0.1382', '-0.4119', '-0.083', '0.08026', '-0.2296', '-0.724', '0.10736', '-0.5264', '0.7783', '-0.1292', '0.3484', '-0.1437', '-0.11743', '0.421', '0.00531', '-0.2383', '0.464', '0.855', '0.4597', '0.04166', '0.1416', '-0.2156', '-0.07', '-0.3135', '0.02106', '-0.2568', '-0.5337', '0.05713', '-0.2058', '-0.2206', '-0.3584', '-0.0804', '-0.2588', '-0.4026', '0.2554', '-0.5015', '0.1793', '-0.1199', '0.1863', '0.115', '-0.5903', '0.0658', '0.01151', '-0.4426', '-0.59', '0.3372', '-0.1142', '-0.0467', '0.2157', '-0.379', '0.0329', '-0.3486', '0.1008', '0.2489', '-0.3032', '0.59', '-0.462', '0.04938', '-0.02391', '-0.1055', '0.2012', '-0.1843', '0.3367', '0.3462', '0.41', '-0.2048', '-0.4094', '-0.2133', '-0.2325', '0.3213', '-0.553', '-0.2651', '0.665', '0.13', '0.1368', '-0.04248', '0.736', '0.5186', '-0.323', '-0.2048', '0.755', '0.402', '0.1725', '-0.6636', '-0.2786', '0.144']",,,C537257,,,,
mondo:0009339,congenital bile acid synthesis defect 2,"['congenital bile acid synthesis defect type 2', 'AKR1D1 congenital bile acid synthesis defect', 'bile acid synthesis defect, congenital, 2', 'congenital bile acid synthesis defect caused by mutation in AKR1D1', 'bile acid synthesis defect, congenital, type 2', 'congenital bile acid synthesis defect, type 2', 'CBAS2', 'cholestasis with Delta(4)-3-oxosteroid 5-Beta-reductase deficiency', 'cholestasis with delta(4)-3-oxosteroid 5-beta-reductase deficiency', 'BASD2']",0111069,235555,79303,C1856127,"['-0.0753', '0.3633', '-0.003933', '0.2715', '0.3', '-0.05157', '-0.1461', '0.561', '-0.1956', '0.1904', '-0.593', '-0.3281', '0.3896', '0.4995', '-0.877', '-0.873', '-0.1599', '-0.3335', '-0.1265', '-0.961', '0.10876', '-0.7437', '0.81', '-0.03583', '0.4937', '-0.3005', '0.1508', '0.01895', '-0.4873', '0.0671', '0.4597', '0.5', '0.3035', '0.7993', '-0.06287', '-0.5273', '-0.5327', '-0.1641', '0.553', '0.1833', '0.253', '-0.07666', '0.252', '0.5317', '-0.526', '-0.2935', '0.5796', '-0.294', '0.248', '-0.3376', '0.03326', '-0.02753', '-0.0984', '-0.94', '-0.5337', '0.1261', '-0.1417', '0.04895', '-0.5713', '0.2108', '0.5034', '0.4807', '0.429', '-0.4841', '0.4873', '0.1227', '0.8813', '0.1017', '-0.1766', '0.05902', '0.1454', '0.258', '0.2532', '-0.00804', '0.4888', '-0.1455', '-0.1891', '-0.2908', '-0.1162', '-0.2189', '0.001273', '-0.128', '-0.8965', '-0.424', '-0.4314', '-0.2566', '0.1995', '-0.09906', '0.5093', '-0.053', '0.662', '0.2937', '-0.03735', '0.0315', '0.515', '0.1569', '0.1746', '-0.617', '-0.1085', '0.10803']",,,C535443,,,,
mondo:0009340,non-spherocytic hemolytic anemia due to hexokinase deficiency,"['hexokinase deficiency hemolytic anaemia', 'nonspherocytic hemolytic anaemia due to hexokinase deficiency', 'nonspherocytic hemolytic anemia due to hexokinase deficiency', 'hemolytic anaemia due to hexokinase deficiency', 'hexokinase deficiency hemolytic anemia', 'hemolytic anemia, nonspherocytic, due to hexokinase deficiency', 'hemolytic anemia due to hexokinase deficiency']",,235700,90031,,"['-0.4443', '0.0991', '-0.2333', '0.2585', '0.4395', '-0.01993', '-0.4575', '0.5103', '-0.2418', '-0.53', '0.6343', '0.12396', '0.2488', '0.388', '-1.056', '0.002836', '-0.5127', '0.04657', '-0.607', '-0.362', '-0.17', '-0.4746', '0.1893', '-0.314', '0.6685', '-0.3582', '-0.0637', '-0.2905', '0.515', '0.0775', '0.3186', '0.10736', '0.3857', '0.474', '0.4868', '-0.2201', '-0.869', '-0.6357', '0.51', '0.009056', '-0.8794', '0.1007', '0.04617', '-0.4985', '-0.6733', '-0.774', '0.2476', '0.04956', '0.5845', '-0.463', '0.5537', '0.2861', '0.98', '-0.191', '0.63', '-0.5376', '0.10077', '0.3362', '-0.9478', '0.0524', '0.0995', '0.3228', '-0.2245', '-0.3503', '-0.006786', '0.3', '0.3826', '0.9155', '-0.6724', '0.8184', '0.7783', '-0.4536', '-0.4333', '-0.4128', '0.324', '1.194', '0.1471', '0.5312', '0.1554', '0.6035', '0.2522', '0.107', '0.0735', '0.08203', '0.5073', '-0.4373', '-0.288', '0.405', '0.8784', '-0.1476', '0.52', '0.2783', '-0.3367', '-0.11395', '0.6553', '1.2', '0.1387', '-0.0863', '0.4402', '-0.654']",,,C562995,,,,
mondo:0009341,Mowat-Wilson syndrome,"['Hirschsprung disease intellectual disability syndrome', 'Hirschsprung disease-mental retardation syndrome', 'microcephaly, mental retardation, and distinct facial featrues, with or without Hirschprung disease', 'MOWS', 'intellectual disability, microcephaly, and distinct facial features with or without Hirschsprung disease', 'microcephaly, intellectual disability, and distinct Facial features, with or without Hirschsprung disease', 'microcephaly, mental retardation, and distinct Facial features, with or without Hirschsprung disease', 'Hirschsprung disease-intellectual disability syndrome', 'microcephaly, intellectual disability, and distinct facial featrues, with or without Hirschprung disease', 'Hirschsprung disease mental retardation syndrome', 'Mowat-Wilson syndrome', 'mental retardation, microcephaly, and distinct facial features with or without Hirschsprung disease']",0060485,235730,2152,C1856113,"['-0.04343', '-0.0777', '0.35', '-0.366', '-0.4287', '-0.2893', '0.5425', '1.086', '-0.6113', '-0.855', '-0.286', '-0.2347', '0.1654', '-0.003199', '-0.4082', '0.2117', '0.0696', '-0.522', '-0.292', '-0.4348', '0.1642', '0.2255', '0.2439', '-0.0765', '0.1637', '-0.1178', '-0.1941', '0.0888', '0.544', '-0.4011', '0.2001', '-0.729', '0.2128', '0.2305', '-0.0669', '-0.3015', '-0.3623', '-0.1399', '-0.2603', '0.609', '0.12317', '0.0398', '0.1871', '0.02985', '0.557', '0.3984', '-0.2659', '0.3784', '-0.565', '-0.09784', '-0.2219', '0.4402', '-0.2527', '-0.2146', '-0.2166', '-0.0799', '-0.199', '0.1332', '-0.1991', '-0.359', '-0.2593', '0.479', '0.3342', '-0.07947', '0.369', '0.2296', '0.8477', '-0.10236', '-0.2246', '0.573', '0.1765', '0.1059', '-0.1096', '0.542', '0.009735', '0.3506', '0.2913', '-0.3733', '-0.7744', '-0.1442', '-0.1326', '-0.04974', '-0.2483', '1.0', '-0.092', '-0.02939', '0.4663', '0.3489', '-0.004856', '0.709', '-0.1343', '0.7637', '0.4712', '0.303', '0.6553', '-0.1376', '0.1992', '-0.489', '0.1827', '0.178']",C74999,,C536990,759.89,,,
mondo:0009342,Hirschsprung disease-hearing loss-polydactyly syndrome,"['Santos-Mateus-Leal syndrome', 'Santos Mateus Leal syndrome', 'Hirschsprung disease-deafness-polydactyly syndrome', 'Hirschsprung disease with polydactyly, renal agenesis, and deafness', 'Hirschsprung disease associated with polydactyly, unilateral renal agenesis, hypertelorism, and congenital deafness', 'Hirschsprung disease, deafness and polydactyly']",,235740,2155,,,,,C565518,,,,
mondo:0009343,"Hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect","['Hirschsprung disease polydactyly heart disease', 'Hirschsprung disease with ulnar polydactyly, polysyndactyly of big toes, and ventricular septal defect']",,235750,,C1856111,,,,C565517,,,,
mondo:0009344,Hirschsprung disease-nail hypoplasia-dysmorphism syndrome,"['Al-Gazali-Donnai-Mueller syndrome', 'Hirschsprung^s disease, hypoplastic nails, and minor dysmorphic features', 'Al Gazali-Donnai-Muller syndrome', 'Hirschsprung disease with hypoplastic nails and dysmorphic facial features']",,235760,2153,,,,,C535615,,,,
mondo:0009345,histidinemia,"['histidine ammonia-lyase deficiency', 'Histidinuria', 'histidinuria', 'Hal deficiency', 'HIS deficiency', 'histidinemia', 'histidase deficiency', 'hyperhistidinemia']",0060168,235800,2157,C0220992,"['-0.4414', '0.267', '0.06067', '0.1482', '-0.1426', '-0.1395', '-0.257', '0.5356', '-0.3862', '0.1691', '-0.1133', '-0.2496', '0.4202', '0.1181', '0.1294', '0.2125', '0.07245', '-0.0723', '-0.6475', '-0.618', '0.1833', '-0.6777', '0.792', '0.0876', '0.268', '-0.7876', '0.1249', '0.1978', '-0.0853', '0.1803', '1.141', '-0.4238', '0.091', '0.02766', '-0.484', '-0.1346', '0.1681', '-0.04617', '0.4517', '-0.1965', '0.4353', '-0.2856', '0.3584', '-0.6445', '-0.1525', '-0.4172', '0.2935', '-0.3335', '0.312', '0.2825', '0.0676', '0.3044', '-0.574', '-0.537', '0.1527', '0.2228', '-0.2008', '-0.4648', '-0.2001', '0.5225', '0.04205', '-0.2556', '0.1517', '-0.288', '0.09576', '0.265', '0.5337', '-0.003592', '-0.4316', '-0.0955', '-0.1533', '0.2155', '0.05917', '0.1471', '-0.0774', '0.3108', '0.7095', '0.2073', '0.1765', '0.2421', '0.02794', '0.006565', '-0.0884', '0.4717', '0.0899', '0.297', '-0.11346', '-1.034', '0.6465', '0.1516', '0.401', '0.2976', '-0.2761', '-0.558', '0.971', '0.4421', '0.02371', '-0.4963', '0.1477', '0.1758']",,,C538320,,E70.41,,
mondo:0009346,histidinuria due to a renal tubular defect,"['histidinuria due to a renal tubular defect', 'histidinuria-renal tubular defect syndrome']",,235830,2158,C0268642,,,,C538321,,,,
mondo:0009347,familial lipochrome histiocytosis,"['histiocytosis, familial lipochrome']",,235900,,C0334125,,,,C562738,,,,
mondo:0009348,classic Hodgkin lymphoma,"['Chl', 'classical Hodgkin lymphoma', 'Hodgkin disease', 'Hodgkin lymphoma, susceptibility to', 'classical Hodgkin^s lymphoma', 'classic Hodgkin disease', 'lymphoma, Hodgkin, classic']",,236000,391,CN204952,"['-0.0082', '0.04736', '-0.00083', '-0.01182', '0.003038', '-0.05826', '-0.00401', '0.04517', '-0.01904', '-0.02354', '-0.004955', '-0.006058', '-0.01337', '-0.000662', '0.00707', '-0.0389', '-0.0152', '-0.0291', '0.001321', '-0.0785', '-0.0199', '-0.03903', '0.0679', '-0.003052', '0.02742', '-0.02483', '-0.004177', '-0.01165', '-0.006214', '-0.03906', '0.04178', '0.00957', '0.05078', '0.007187', '0.03065', '-0.003338', '-0.03918', '0.00691', '-0.005737', '-0.03622', '0.01389', '-0.05936', '0.01604', '-0.03632', '0.01224', '-0.03522', '-0.02997', '0.03485', '0.00967', '0.03586', '-0.0184', '-0.01133', '0.00311', '-0.00223', '-0.04337', '-0.02248', '0.02603', '-0.02843', '-0.04022', '-0.01266', '0.03114', '0.01012', '-7.59e-05', '0.00772', '0.01003', '0.007107', '0.04816', '0.0441', '-0.03232', '0.0935', '-0.02197', '0.01487', '0.007313', '-0.0206', '0.03516', '0.0351', '-0.001051', '-0.00885', '-0.0234', '-0.05145', '-0.01547', '-0.02051', '-0.03714', '0.03677', '-0.05005', '-0.01598', '0.02768', '-0.00826', '0.05582', '-0.01052', '0.01695', '0.01915', '0.015076', '0.01552', '0.10565', '0.0419', '0.03818', '-0.0419', '-0.03105', '-0.00245']",C7164,,,,,,
mondo:0009349,holoprosencephaly 1,"['holoprosencephaly, familial Alobar', 'HPE1', 'cyclopia', 'holoprosencephaly type 1', 'holoprosencephaly 1, isolated cases', 'isolated arhinencephaly', 'holoprosencephaly 1', 'arhinencephaly', 'Hpe, familial', 'Demyer sequence']",0110881,236100,268936,,,C75476,,,,,,
mondo:0009350,Holzgreve-Wagner-Rehder syndrome,"['cleft palate-Potter sequence-congenital heart anomalies-mesoaxial polydactyly-multiple malformations syndrome', 'Holzgreve Wagner Rehder syndrome', 'Complex congenital heart defect, renal agenesis and cleft lip and palate', 'Holzgreve syndrome']",0060566,236110,2167,C1856095,,,,C535327,,,,
mondo:0009351,homocarnosinosis,"['homocarnosinosis', 'Homocarnosinase deficiency']",0060177,236130,2168,C3495554,,,,C535328,277.89,,,
mondo:0009352,classic homocystinuria,"['homocystinuria due to cystathionine beta-synthase deficiency', 'homocystinuria with or without response to pyridoxine', 'CBS deficiency', 'homocystinuria due to CBS deficiency', 'cystathionine beta-synthase deficiency', 'hyperhomocysteinemia, thrombotic, CBS-related', 'homocystinuria, B6-responsive and nonresponsive types', 'thrombosis, hyperhomocysteinemic']",,236200,394,C0751202,"['0.2998', '0.1699', '-0.0371', '0.265', '0.3691', '-0.3586', '-0.1351', '0.544', '-0.4346', '-0.1409', '-0.1514', '-0.2109', '0.10614', '-0.00541', '-0.505', '-0.1676', '-0.2046', '-0.2651', '-0.333', '-0.1968', '0.007137', '-0.3472', '0.355', '-0.2441', '-0.01261', '0.3423', '0.1394', '0.1597', '-0.333', '0.0983', '0.574', '-0.1586', '-0.446', '0.2319', '-0.3118', '-0.1414', '0.0334', '-0.5522', '0.1906', '0.03848', '-0.0833', '-0.1967', '1.159', '-0.3281', '-0.0709', '-0.3298', '0.5063', '0.1497', '-0.6543', '0.08984', '-0.06464', '0.1649', '0.11176', '-0.1261', '0.0493', '0.1375', '0.4458', '-0.5303', '-0.3267', '0.2148', '0.221', '0.003492', '-0.1792', '0.11816', '-0.201', '0.734', '0.285', '0.02403', '-0.05417', '0.352', '0.3865', '-0.166', '-0.259', '-0.2252', '-0.08356', '0.393', '0.04703', '-0.6123', '-0.1398', '-0.4197', '0.01468', '-0.2424', '-0.1304', '0.4824', '-0.278', '0.5527', '0.0464', '-0.1411', '0.293', '-0.496', '-0.0869', '0.2876', '-0.2313', '-0.1342', '0.383', '0.602', '0.278', '-0.3025', '0.1602', '-0.1824']",,,,,,10071093,
mondo:0009353,homocystinuria due to methylene tetrahydrofolate reductase deficiency,"['5,10-alpha-methylenetetrahydro-folate reductase deficiency', 'MTHFR deficiency, thermolabile type', 'Methylenetetrahydro-folate reductase deficiency', 'homocystinuria due to MTHFR deficiency', 'MTHFR deficiency', 'homocystinuria due to deficiency of N(5,10)-methylenetetrahydrofolate reductase activity', 'Homocysteinemia due to methylenetetrahydro-folate reductase deficiency', 'methylene tetrahydrofolate reductase deficiency', 'methylenetetrahydrofolate reductase deficiency', 'Homocysteinuria due to methylenetetrahydro-folate reductase deficiency', '5,10 alpha methylenetetrahydro-folate reductase deficiency']",,236250,395,,"['-0.2262', '0.1587', '-0.27', '-0.0648', '-0.1307', '-0.6377', '0.1116', '0.4036', '-0.4895', '0.08923', '-0.9062', '0.2402', '-0.0709', '0.01038', '-0.05844', '-0.1929', '0.0823', '-0.2969', '-0.6865', '-0.5005', '0.06366', '-0.3298', '0.32', '-0.569', '-0.04645', '-0.02417', '0.2776', '-0.2588', '-0.3704', '0.01837', '0.2708', '0.0417', '-0.2395', '0.543', '-0.193', '0.08307', '-0.1836', '-0.3618', '-0.356', '0.289', '0.11096', '-0.3672', '0.3687', '0.0826', '-0.324', '-0.425', '0.309', '0.0306', '-0.1598', '0.2505', '0.00409', '0.0949', '0.0662', '-0.1844', '0.2241', '-0.1073', '0.5425', '-0.351', '-0.2227', '0.301', '0.0394', '0.08734', '0.5425', '0.0822', '0.03934', '0.492', '0.4116', '0.1533', '-0.1123', '0.4556', '0.09125', '-0.2195', '-0.569', '-0.298', '0.04843', '0.524', '0.6333', '-0.175', '0.11273', '0.2588', '0.3547', '-0.09875', '-0.5786', '0.2808', '0.673', '0.04535', '-0.273', '0.2461', '0.8086', '-0.0476', '0.3967', '0.2805', '-0.06854', '-0.4333', '0.1736', '0.1592', '0.3015', '-0.0921', '0.1134', '-0.1741']",,,C537357,,,,
mondo:0009354,methylcobalamin deficiency type cblE,"['HMAE', 'homocystinuria-megaloblastic anemia, cbl e type', 'methylmalonic aciduria and homocystinuria type cblE', 'vitamin B12-responsive homocystinuria, cblE type', 'homocystinuria due to defect in methylation Cbl e', 'homocystinuria-megaloblastic Anemia due to defect in cobalamin metabolism, cblE complementation type', 'methylcobalamin deficiency, cblE type', 'homocystinuria-megaloblastic anemia, cblE complementation type', 'functional methionine synthase deficiency type cblE', 'homocystinuria-megaloblastic Anaemia due to defect in cobalamin metabolism, cblE complementation type']",0112255,236270,2169,C1856057,"['-0.288', '0.4543', '0.05597', '-0.1628', '0.3066', '-0.4646', '-0.3503', '0.04123', '-0.1307', '-0.3171', '-0.1766', '0.1465', '0.1287', '-0.291', '0.04202', '-0.2197', '-0.008896', '-0.2302', '-0.2554', '-0.562', '0.2155', '-0.272', '0.2117', '-0.05145', '0.1267', '0.09247', '0.2389', '-0.03087', '0.06256', '-0.1373', '-0.01787', '0.2256', '0.1423', '0.1964', '-0.04175', '-0.1014', '-0.014084', '-0.53', '-0.1282', '-0.2426', '-0.07983', '-0.4202', '0.2734', '0.01883', '-0.3574', '-0.453', '0.0894', '0.08307', '0.2231', '0.0709', '-0.09937', '-0.2144', '-0.06165', '-0.01973', '0.06146', '-0.2186', '0.4587', '0.153', '-0.633', '0.383', '0.2083', '0.2338', '0.3997', '-0.2585', '0.2805', '-0.01682', '0.2343', '0.05402', '-0.3745', '0.1383', '-0.284', '-0.3762', '-0.3013', '-0.08185', '0.06903', '0.3171', '0.2213', '-0.03552', '-0.1285', '0.08514', '0.2937', '0.02681', '-0.0467', '0.066', '0.3777', '0.165', '0.09985', '0.4387', '0.5713', '0.2153', '0.2072', '0.1042', '0.1062', '-0.461', '0.711', '0.612', '0.2852', '-0.4736', '0.07324', '0.07513']",C142173,0005568,C565510,,,,
mondo:0009355,Hooft disease,"['Hooft disease', 'delayed physical development, erythematosquamous eruption, opaque leukonychia, intellectual disability, and low serum lipids']",,236300,,C0268479,,,,C535329,,,,
mondo:0009356,autosomal recessive humeroradial synostosis,"['humeroradial/multiple synostosis syndrome', 'humeroradial synostosis (disease), autosomal recessive', 'humeroradial synostosis']",,236400,,,,,,,,,,
mondo:0009357,humeroradial synostosis with craniofacial anomalies,['humeroradial synostosis with craniofacial anomalies'],,236410,,C1968717,,,,C566888,,,,
mondo:0009358,Hutterite cerebroosteonephrodysplasia syndrome,"['cond', 'Hutterite cerebroosteonephrodysplasia syndrome', 'cerebroosteonephosis syndrome']",,236450,,C1856054,,,,C536074,,,,
mondo:0009359,multinucleated neurons-anhydramnios-renal dysplasia-cerebellar hypoplasia-hydranencephaly syndrome,"['MARCH syndrome', 'hydranencephaly with renal aplasia-dysplasia', 'MARCH', 'multinucleated neurons, anhydramnios, renal dysplasia, cerebellar hypoplasia, and hydranencephaly', 'multinucleated neurons, anhydramnios, renal dysplasia, cerebellar Hypoplasia, and hydranencephaly']",0080327,236500,500135,C1856053,,,,C565507,,,,
mondo:0009360,"hydrocephalus, nonsyndromic, autosomal recessive 1","['hydrocephalus, congenital, 1', 'hydrocephalus, nonsyndromic, autosomal recessive 1', 'ventriculomegaly', 'CCDC88C congenital hydrocephalus', 'hydrocephalus, nonsyndromic, autosomal recessive type 1', 'hydrocephaly', 'congenital hydrocephalus caused by mutation in CCDC88C', 'HYC1']",,236600,,C3887608,,,,,,,,
mondo:0009361,autosomal recessive hydrocephalus due to congenital stenosis of aqueduct of Sylvius,"['aqueductal stenosis', 'hydrocephalus due to congenital stenosis of aqueduct of Sylvius']",,236635,,CN074258,,,,,,,,
mondo:0009362,growth delay-hydrocephaly-lung hypoplasia syndrome,"['retarded growth, hydrocephalus, micrognathia, intestinal malrotation, omphalocele, short lower limbs and foot deformities', 'game-Friedman-Paradice syndrome', 'game Friedman Paradice syndrome', 'hydrocephalus with associated malformations']",,236640,3035,C1856052,,,,C535406,,,,
mondo:0009363,hydrocephaly-tall stature-joint laxity syndrome,"['hydrocephalus, tall stature, joint laxity and kyphoscoliosis', 'Daish-Hardman-Lamont syndrome', 'hydrocephalus, tall stature, JOINT laxity, and kyphoscoliosis', 'hydrocephaly - tall stature - joint laxity', 'Daish Hardman Lamont syndrome']",,236660,2181,C1856051,,,,C535770,,,,
mondo:0009364,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A1","['MDDGA1', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 1', 'hard syndrome', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 1', 'hydrocephalus, agyria, and retinal dysplasia', 'cerebroocular dysplasia-muscular dystrophy syndrome', 'Walker-Warburg syndrome or muscle-eye-brain disease, Pomt1-related', 'cod-MD syndrome', 'muscle-eye-brain-POMT1 related']",0111237,236670,899,CN033898,"['-0.0887', '-0.0419', '-0.06976', '0.2272', '0.1628', '-0.452', '0.02602', '0.04895', '-0.6978', '-0.716', '-0.2347', '-0.6377', '-0.1246', '0.2515', '-0.013275', '0.05908', '-0.0584', '-0.2634', '-0.594', '-0.7095', '0.022', '0.03946', '0.3157', '0.1395', '0.09753', '-0.46', '-0.4033', '0.06525', '0.1017', '0.3682', '0.226', '0.1458', '0.4468', '0.128', '0.1523', '-0.0619', '0.02975', '-0.1073', '0.02374', '-0.11444', '0.2886', '-0.3042', '-0.3516', '0.0951', '0.2334', '-0.0377', '0.1494', '0.2642', '0.3555', '-0.1781', '0.1614', '0.1648', '-0.04752', '-0.3542', '0.177', '0.04288', '-0.2262', '0.2666', '-0.001976', '0.09436', '-0.04727', '-0.506', '0.1421', '0.3958', '-0.6016', '0.04236', '-0.01158', '0.5684', '-0.5996', '0.1339', '-0.3828', '0.1742', '0.02483', '0.2261', '0.3816', '-0.1737', '0.3855', '-0.4229', '-0.3267', '-0.06714', '0.4958', '0.16', '-0.7793', '0.8457', '-0.583', '-0.1417', '0.4285', '0.487', '0.4006', '0.4993', '-0.2532', '0.2747', '-0.1273', '0.1849', '0.3442', '0.1594', '0.3809', '0.1996', '0.2277', '0.08105']",C128118,,,,,,
mondo:0009365,hydrolethalus syndrome 1,"['HYLS1 hydrolethalus syndrome', 'hydrolethalus syndrome caused by mutation in HYLS1', 'hydrolethalus syndrome type 1', 'HLS1', 'hydrolethalus syndrome', 'hydrolethalus syndrome 1']",0111355,236680,,C1856016,,,,C565504,,,,
mondo:0009366,normal pressure hydrocephalus,"['chronic adult hydrocephalus', 'hydrocephalus, normal-pressure', 'NPH', 'low pressure hydrocephalus', 'hydrocephalus, normal pressure, 1']",1572,236690,314928,C0020258,"['-0.2815', '-0.05197', '0.04724', '0.591', '-0.3196', '-0.2452', '0.0119', '0.5396', '-0.566', '0.865', '-0.2185', '-0.9136', '-0.593', '0.2576', '0.452', '-0.281', '-0.3606', '-0.00312', '-0.6343', '-1.284', '-0.10785', '-0.1936', '0.385', '-0.3054', '-0.1732', '-0.522', '-0.724', '0.9604', '-0.558', '0.517', '-0.6426', '-1.069', '0.434', '0.02556', '-0.3477', '0.5337', '-0.3655', '0.1602', '-0.05606', '-0.5967', '0.8955', '0.3862', '0.168', '-0.6475', '0.8335', '-0.3103', '0.5527', '-0.697', '0.332', '0.4995', '0.4607', '0.2537', '-0.2996', '-0.9785', '0.4016', '-0.2124', '0.0449', '0.1663', '-0.02284', '0.3157', '-0.2559', '0.73', '-0.466', '-0.0854', '0.0779', '0.4355', '0.1812', '-0.0238', '-0.8506', '0.2273', '-0.04004', '1.038', '0.0638', '-0.955', '0.2693', '0.693', '0.182', '1.006', '-0.1616', '-0.982', '-0.328', '-0.06055', '-0.3616', '0.544', '0.3591', '0.894', '0.6465', '-0.0256', '0.5977', '-0.3086', '-0.1606', '0.906', '0.2258', '0.1758', '0.6763', '0.505', '0.455', '-0.2505', '-0.11957', '0.1481']",,1001065,D006850,331.5,,10029773,
mondo:0009367,McKusick-Kaufman syndrome,"['hydrometrocolpos-postaxial polydactyly syndrome', 'McKusick Kaufman syndrome', 'MKKS', 'MCKUSICK-Kaufman syndrome', 'hydrometrocolpos syndrome', 'hydrometrocolpos, postaxial polydactyly, and congenital heart malformation', 'Kaufman-Mckusick syndrome', 'Kaufman McKusick syndrome', 'McKusick-Kaufman syndrome', 'HMCS']",0111255,236700,2473,C0948368,"['-0.436', '-0.0792', '-0.07715', '-0.3704', '0.1355', '-0.3486', '0.02257', '0.352', '-0.08636', '-0.4478', '0.11383', '-0.4182', '-0.2695', '0.3933', '-0.2534', '-0.3303', '-0.2454', '-0.1725', '-0.4263', '-0.389', '0.1681', '-0.04007', '0.5576', '-0.1918', '0.0707', '0.02782', '-0.3008', '0.0629', '0.629', '-0.1624', '0.3645', '-0.2908', '0.144', '0.4128', '0.3235', '-0.2969', '-0.1627', '-0.1835', '-0.207', '0.2583', '-0.143', '0.268', '0.1287', '-0.372', '0.198', '-0.3154', '-0.09674', '0.1844', '-0.3809', '0.1622', '-0.1508', '0.004658', '-0.0729', '-0.1755', '-0.4062', '-0.1511', '0.0762', '0.03912', '-0.2544', '0.352', '0.317', '0.2253', '0.0663', '0.0947', '-0.1389', '0.2131', '0.1293', '0.1123', '-0.3079', '0.471', '-0.5513', '-0.05447', '0.2517', '0.0802', '0.08716', '-0.2245', '0.1522', '-0.1752', '-0.4485', '-0.2861', '-0.2112', '0.2407', '0.0737', '0.344', '0.11536', '0.0826', '0.1783', '-0.1377', '0.0695', '-0.1703', '0.01493', '0.059', '0.439', '0.0363', '0.6426', '-0.3264', '0.6074', '-0.2876', '0.3293', '0.193']",,,C538159,758.89,,10052312,
mondo:0009368,urofacial syndrome type 1,"['urofacial syndrome 1', 'inverted smile and occult neuropathic bladder', 'UFS1', 'hydronephrosis with peculiar Facial expression', 'Ochoa syndrome', 'urofacial syndrome type 1', 'facial palsy, partial, with urinary abnormalities', 'urofacial syndrome']",,236730,,,,,,,,,,
mondo:0009369,non-immune hydrops fetalis,"['non-immune HF', 'Haemoglobin H hydrops fetalis syndrome', 'non-immune foetal hydrops', 'non-immune fetal edema', 'hydrops fetalis, Alpha-thalassemia-related', 'non-immune foetal oedema', 'Hemoglobin H hydrops fetalis syndrome', 'hydrops fetalis, nonimmune', 'non-immune fetal hydrops', 'NIHF']",,236750,363999,C0455988,,C111905,0009051,,778.0,,,
mondo:0009370,L-2-hydroxyglutaric aciduria,"['L-2-hydroxyglutaric aciduria', 'L-2-HGA', 'L-2-hydroxyglutaric acidemia', 'L2HGA']",0050574,236792,79314,C3888081,"['-0.0412', '0.1333', '-0.04587', '-0.374', '-0.274', '-0.87', '-0.0193', '1.119', '-0.745', '-0.1702', '-0.5703', '-0.08484', '-0.0678', '-0.0364', '0.649', '0.0372', '0.2734', '-0.2966', '-0.344', '-0.6816', '0.3877', '-0.3247', '-0.0666', '-0.42', '0.1992', '-0.2751', '-0.1327', '0.0716', '-0.6', '0.1644', '0.259', '0.1886', '0.01778', '-0.4604', '-0.1231', '0.4207', '-0.4458', '-0.6123', '-0.259', '0.0707', '-0.01063', '-0.6523', '0.2537', '-0.228', '0.2622', '-0.531', '0.5366', '-0.1713', '-0.1824', '-0.0891', '0.1508', '0.567', '-0.5757', '-0.3894', '0.387', '-0.09033', '0.127', '-0.145', '-0.608', '0.7656', '-0.01418', '-0.2588', '0.3691', '-0.2827', '-0.01819', '0.3958', '0.271', '-0.1176', '-0.7114', '0.7173', '-0.1959', '-0.0654', '-0.4307', '-0.2119', '0.157', '0.3064', '0.365', '-0.2479', '-0.141', '0.4177', '0.06934', '-0.3486', '-0.3586', '0.4368', '0.1014', '0.2217', '-0.003157', '0.08325', '0.724', '-0.1443', '0.4158', '0.3167', '-0.4717', '0.07416', '0.088', '0.3535', '0.541', '0.10956', '0.4143', '-0.269']",,,,,,,
mondo:0009371,3-hydroxyisobutyric aciduria,"['disorder of valine metabolism', '3-hydroxyisobutyric aciduria']",,236795,939,C0342737,,,,C535312,791.9,,,
mondo:0009372,encephalopathy due to hydroxykynureninuria,"['hydroxykynureninuria', 'kynureninase deficiency, partial', 'Xanthurenic aciduria', 'kynureninase deficiency']",0112257,236800,79155,C0268474,"['-0.3762', '0.1511', '-0.1036', '-0.3948', '0.2228', '-0.4502', '-0.2473', '0.422', '-0.2427', '0.02776', '-0.386', '-0.2094', '-0.07294', '-0.1552', '-0.03815', '-0.1031', '0.3599', '-0.05823', '-0.4', '-0.7017', '0.1359', '-0.1456', '0.1073', '-0.4355', '0.02643', '-0.2466', '0.1001', '-0.268', '0.0431', '-0.0363', '0.189', '0.231', '0.2998', '0.2323', '-0.5825', '-0.08545', '-0.3367', '-0.03802', '-0.2605', '-0.1803', '-0.02208', '-0.319', '0.00128', '-0.1268', '-0.2622', '-0.274', '0.1787', '0.08875', '-0.2507', '0.0923', '-0.10596', '0.2151', '-0.2917', '-0.3796', '0.0893', '-0.0368', '0.4414', '-0.2329', '-0.4272', '0.2998', '0.0893', '0.08905', '0.2224', '-0.2915', '0.0838', '-0.2532', '0.2896', '0.4595', '-0.3145', '-0.1157', '-0.2698', '0.552', '-0.0938', '-0.00278', '0.2517', '0.3574', '0.422', '-0.2272', '-0.10876', '0.227', '0.1448', '0.2202', '0.1862', '0.2654', '0.3733', '0.4011', '-0.0752', '0.1523', '0.1431', '0.1989', '0.3499', '0.5845', '-0.1392', '-0.2256', '0.4727', '0.619', '0.2395', '-0.3633', '0.115', '0.02107']",,,C536081,270.2,,,
mondo:0009373,seizures-intellectual disability due to hydroxylysinuria syndrome,['hydroxylysinuria'],,236900,79156,C1855986,,,,C565502,,,,
mondo:0009374,hydroxyprolinemia,"['Hydroxyprolinemia', '4 alpha hydroxy-L-proline oxidase deficiency', 'hydroxyprolinemia (disease)', 'HYDROXYPROLINEMIA', '4-hydroxy-L-proline oxidase deficiency']",,237000,,C0268531,,,,C562669,270.8,,,0003260
mondo:0009375,"hymen, imperforate","['hymen, imperforate']",,237100,,,,,,C562397,752.42,Q52.3,,
mondo:0009376,carbamoyl phosphate synthetase I deficiency disease,"['deficiency disease', 'hyperammonemia due to carbamoyl phosphate synthetase 1 deficiency', 'CPS 1 deficiency', 'carbamoyl phosphate synthetase I deficiency, hyperammonemia due to', 'carbamoyl phosphate synthetase 1 deficiency', 'carbamoyl-phosphate synthetase 1 deficiency', 'carbamyl phosphate synthetase (CPS) deficiency', 'CPS1 deficiency', 'carbamoyl-phosphate synthase', 'CPS I deficiency', 'carbamoyl phosphate synthetase deficiency', 'carbamoyl-phosphate synthetase deficiency', 'carbamoylphosphate synthetase I deficiency', 'carbamoyl phosphate synthetase 1 deficiency, hyperammonemia due to', 'carbamoyl-phosphate synthetase I deficiency', 'CPS1D']",9280,237300,147,,"['-0.010414', '0.5503', '-0.3555', '-0.1791', '0.02481', '-0.0807', '-0.2155', '0.484', '-0.708', '-0.2983', '-0.4731', '-0.4138', '0.1501', '0.2732', '-0.342', '-0.0744', '-0.3042', '-0.376', '-0.3257', '-0.863', '-0.2578', '-0.1982', '0.6694', '-0.00229', '-0.1691', '-0.7783', '-0.2925', '-0.2512', '0.05072', '0.01945', '0.3418', '0.3281', '0.3572', '0.8164', '-0.629', '0.3848', '0.04843', '-0.1813', '0.04306', '-0.06158', '0.2063', '-0.7803', '0.646', '0.2861', '-0.4849', '-0.2744', '-0.6025', '-0.633', '0.02374', '0.9795', '-0.4084', '-0.01678', '0.008804', '-0.9673', '0.3188', '0.4626', '0.6323', '0.3452', '-0.1337', '0.1818', '0.12427', '0.1128', '0.5415', '-0.2703', '-0.102', '0.927', '1.023', '0.11633', '-0.5386', '-0.01405', '-0.2776', '0.5728', '-0.3442', '-0.06824', '0.465', '0.2219', '0.4424', '-0.4358', '-0.866', '-0.3547', '-0.04684', '-0.0771', '-0.695', '-0.8027', '1.051', '0.904', '0.323', '0.2312', '0.8784', '-0.1826', '0.2279', '0.4197', '-0.4067', '-0.1268', '-0.4724', '0.4363', '0.1678', '-0.1517', '-0.06934', '0.1205']",C84612,0007193,D020165,,,10058297,
mondo:0009377,hyperammonemia due to N-acetylglutamate synthase deficiency,"['NAGSD', 'N-acetyl glutamate synthetase deficiency', 'NAGS deficiency', 'N-acetylglutamate synthase deficiency', 'NAG synthetase deficiency', 'N-acetylglutamate synthetase deficiency', 'Nags deficiency', 'hyperammonemia due to N-acetylglutamate synthetase deficiency']",0112258,237310,927,,"['-0.479', '0.3206', '-0.2668', '0.11975', '-0.0337', '-0.3884', '0.5605', '0.2615', '-0.1426', '0.228', '-0.3364', '-0.2085', '-0.11584', '-0.11127', '-0.17', '0.11835', '-0.1152', '-0.1947', '-0.637', '-0.928', '-0.3958', '-0.2415', '0.5356', '-0.5073', '-0.09534', '-0.3152', '0.1124', '-0.1326', '-0.01581', '0.0806', '0.3647', '0.518', '0.09216', '0.36', '-0.4866', '-0.13', '0.1938', '-0.2996', '-0.0552', '0.1858', '0.227', '-0.3557', '0.2024', '0.1732', '-0.1578', '-0.2542', '0.05426', '-0.3384', '-0.08624', '0.7456', '-0.2272', '-0.03766', '-0.0839', '-0.2158', '0.314', '-0.04486', '0.4683', '0.1324', '-0.3208', '0.2532', '0.334', '0.6006', '0.2632', '-0.1632', '0.3142', '0.04083', '0.4373', '-0.09985', '-0.5454', '0.01147', '-0.4336', '-0.03082', '-0.1626', '-0.05557', '0.1875', '0.2313', '0.3826', '-0.5503', '-0.2156', '0.01282', '0.2355', '0.219', '-0.4856', '0.002163', '0.5576', '0.535', '0.1611', '0.1661', '0.5986', '0.02792', '0.217', '0.56', '-0.2905', '-0.3596', '0.2018', '0.5464', '0.067', '-0.549', '0.472', '-0.3164']",C129307,,C536109,,,,
mondo:0009378,hyper-beta-alaninemia,"['hyperalaninemia', 'hyperbetaalaninemia', 'hyper-beta-alaninemia']",,237400,309147,C0268630,,,,C562684,270.8,,,
mondo:0009379,Rotor syndrome,"['Rotor-type hyperbilirubinemia', 'hyperbilirubinemia, rotor type, digenic', 'HBLRR', 'hyperbilirubinemia, ROTOR type', 'hyperbilirubinemia, Rotor type', 'Rotor syndrome']",,237450,3111,C0220991,"['0.0672', '-0.03003', '-0.2118', '-0.0317', '0.03864', '-0.11774', '-0.0614', '0.7827', '0.3184', '0.4463', '0.212', '0.1852', '-0.03717', '-0.07745', '-0.2632', '0.04434', '0.078', '-0.03357', '-0.01852', '-0.6816', '-0.06042', '-0.341', '0.811', '-0.1309', '-0.01953', '-0.0984', '-0.1632', '-0.3965', '0.206', '-0.2742', '0.2445', '-0.2068', '-0.1152', '0.0659', '-0.5806', '-0.358', '-0.616', '-0.6553', '0.2086', '0.1103', '-0.2512', '-0.406', '0.3079', '-0.328', '0.3806', '-0.01738', '-0.0652', '-0.10254', '0.06415', '0.1935', '-0.3005', '0.1993', '-0.2827', '-0.0652', '0.1694', '0.01566', '0.2795', '-0.2847', '-0.5527', '0.0729', '0.5073', '0.3022', '0.3286', '-0.3352', '-0.088', '-0.4717', '0.08386', '0.1958', '-0.1987', '0.2251', '-0.2812', '-0.193', '-0.09656', '0.12146', '0.3716', '0.1065', '0.349', '-0.2803', '0.3896', '-0.03894', '0.1519', '0.4507', '-0.1632', '-0.1521', '-0.2043', '-0.001285', '0.19', '-0.1089', '0.43', '-0.2455', '0.5547', '0.1466', '0.35', '-0.2986', '1.101', '0.2761', '-0.00099', '-0.9727', '-0.3557', '-0.07983']",,,,,,10039234,
mondo:0009380,Dubin-Johnson syndrome,"['Dubin-Johnson syndrome', 'hyperbilirubinemia 2', 'hyperbilirubinemia type 2', 'Dubin Johnson syndrome', 'Dubin-Sprinz disease', 'conjugated hyperbilirubinemia', 'hyperbilirubinemia, Dubin-Johnson type', 'chronic idiopathic jaundice', 'Sprinz-Nelson syndrome', 'DJS']",12308,237500,234,C0022350,"['-0.1985', '-0.3394', '-0.335', '-0.3687', '0.1893', '0.247', '0.03738', '0.3074', '0.2927', '0.383', '-0.07', '0.3901', '-0.276', '0.089', '-0.4875', '-0.2808', '0.4019', '-0.1622', '-0.1603', '-0.542', '0.09106', '-0.8135', '0.741', '-0.07385', '-0.5957', '-0.1743', '-0.298', '0.3103', '-0.404', '-0.311', '0.5083', '-0.4397', '-0.02872', '-0.01204', '-0.423', '-0.1774', '-0.5664', '-0.299', '0.2827', '0.1827', '-0.0546', '-0.6553', '0.1428', '-0.1317', '-0.1232', '0.2634', '0.2993', '0.1733', '0.07245', '0.1704', '0.223', '0.10785', '-0.1942', '-0.261', '0.1595', '0.2065', '0.6216', '-0.2023', '-0.792', '0.176', '0.635', '0.365', '0.4792', '-0.515', '-0.625', '-0.2021', '0.414', '0.0473', '-0.3936', '0.2241', '-0.06415', '-0.2537', '0.06006', '0.5234', '0.423', '0.1431', '0.727', '0.148', '0.144', '-0.2104', '0.3047', '0.01788', '0.37', '0.1125', '-0.4053', '0.0423', '-0.1531', '0.428', '0.3489', '-0.1841', '0.6914', '0.2734', '-0.09033', '-0.2377', '1.035', '0.334', '-0.3052', '-0.777', '-0.4546', '-0.1335']",C34741,,D007566,,,10013800,
mondo:0009381,"hyperbilirubinemia, conjugated, type 3","['hyperbilirubinemia, conjugated, type III']",,237550,,C0400964,,,,C562885,,,,
mondo:0009382,"hyperbilirubinemia, shunt, primary","['hyperbilirubinemia, shunt, primary', 'PSHB']",,237800,,,,,,,,,,
mondo:0009383,transient familial neonatal hyperbilirubinemia,"['HBLRTFN', 'hyperbilirubinemia, familial transient neonatal', 'Lucey-Driscoll syndrome', 'hyperbilirubinemia transient familial neonatal', 'hyperbilirubinemia, transient familial neonatal', 'breast milk jaundice', 'transient familial hyperbilirubinemia']",,237900,2312,C0270210,"['0.0616', '0.3232', '-0.4082', '0.1472', '-0.10815', '-0.365', '-0.1142', '0.3794', '-0.0846', '0.1459', '0.2094', '-0.1398', '-0.1628', '0.1035', '-0.4524', '0.03137', '0.1377', '-0.03516', '0.0655', '-0.5903', '-0.1332', '-0.1748', '0.2191', '-0.12384', '0.2952', '-0.2194', '-0.05893', '0.3005', '-0.1625', '-0.083', '0.2343', '-0.279', '-0.05408', '0.0737', '-0.5425', '0.426', '-0.1473', '-0.1448', '-0.1875', '0.094', '0.15', '-0.09015', '-0.104', '-0.11835', '-0.3267', '-0.02536', '-0.378', '-0.06158', '-0.1981', '0.2583', '-0.1686', '-0.1442', '0.0729', '0.05527', '-0.0485', '0.1078', '0.168', '-0.2742', '-0.0678', '0.06573', '0.07513', '0.1342', '0.1368', '0.0795', '-0.0714', '-0.05496', '0.4482', '0.3313', '-0.369', '0.448', '-0.05682', '0.4158', '0.2256', '-0.1976', '-0.03372', '0.10156', '0.4004', '0.1123', '-0.0314', '-0.02557', '-0.1055', '-0.2136', '-0.12445', '-0.4822', '0.4854', '0.2458', '0.05798', '0.11053', '0.231', '0.138', '0.316', '0.4143', '0.06805', '0.2201', '0.4775', '0.319', '-0.1389', '-0.4817', '0.2406', '0.0816']",,,C562692,,,,
mondo:0009384,"Leydig cell hypoplasia, type 1","['hypergonadotropic hypogonadism, Male, due to Lhcgr defect', 'Leydig cell hypoplasia, partial', 'leydig cell hypoplasia with pseudohermaphroditism', 'Leydig cell Hypoplasia, type 2', 'Leydig cell hypoplasia caused by mutation in LHCGR', 'Leydig cell hypoplasia, complete', 'Leydig cell hypoplasia with male pseudohermaphroditism', 'Leydig cell hypoplasia, type I', 'luteinizing hormone resistance, female', 'leydig cell hypoplasia with hypergonadotropic hypogonadism', 'LHCGR Leydig cell hypoplasia', 'Leydig cell agenesis']",,238320,,,"['-0.0858', '0.11505', '0.0787', '-0.01907', '0.07324', '-0.10175', '0.0399', '0.11084', '-0.0934', '-0.0904', '-0.0378', '-0.0424', '-0.00674', '-0.02321', '-0.05743', '-0.07574', '0.03967', '-0.0704', '0.01273', '-0.1664', '-0.03857', '-0.1034', '0.1262', '-0.04703', '0.055', '-0.02478', '-0.03336', '-0.0456', '0.001387', '-0.07605', '0.1165', '0.02849', '0.1879', '0.03876', '0.0321', '-0.05963', '-0.04105', '-0.04648', '0.001963', '-0.12115', '0.04907', '-0.0916', '0.03894', '-0.01145', '-0.0838', '-0.1425', '-0.01996', '0.04303', '0.05472', '-0.001115', '0.003763', '-0.02441', '0.02415', '0.004463', '-0.09125', '-0.03308', '0.0769', '-0.0722', '-0.1458', '0.02773', '0.002972', '0.0469', '-0.009995', '0.03784', '0.048', '0.01266', '0.1206', '0.05142', '-0.0912', '0.1672', '-0.0729', '0.03114', '0.02681', '-0.1179', '0.06042', '0.0467', '-0.01729', '-0.03406', '-0.1217', '-0.0857', '-0.01109', '0.0359', '-0.05264', '0.0863', '-0.07245', '-0.01459', '0.03041', '0.1547', '0.1775', '-0.0276', '0.01633', '0.08636', '0.04266', '-0.0665', '0.2114', '0.04062', '0.0845', '-0.2004', '0.0125', '0.0737']",,,,,,,
mondo:0009385,hyperleucine-Isoleucinemia,['hyperleucine-Isoleucinemia'],,238340,,C0268574,,,,C562674,,,,
mondo:0009386,hyperlexia,"['compulsive reading', 'precocious reading', 'hyperlexia']",,238350,,,,,,C565500,,,,
mondo:0009387,familial lipoprotein lipase deficiency,"['familial LPL deficiency', 'familial fat-induced hypertriglyceridemia', 'LPL deficiency', 'hypercholesterinaemic xanthomatosis', 'familial lipoprotein lipase deficiency with type I phenotype', 'chylomicronemia, familial', 'familial chylomiconemia syndrome', 'Fredrickson type I hyperlipoproteinemia', 'lipd deficiency', 'hyperlipoproteinemia, type I', 'hyperchylomicronemia', 'hyperlipoproteinemia, type 1A', 'lipase D deficiency', 'hyperlipemia, idiopathic, Burger-Grutz type', 'mixed hyperglyceridemia', 'familial hyperchylomicronemia', 'familial hyperlipoproteinemia type I', 'hyperlipoproteinemia, type 1', 'hyperlipoproteinemia type I', 'hyperchylomicronemia, familial', 'lipoprotein lipase deficiency', 'type I hyperlipoproteinemia', 'hyperlipemia, essential familial', 'endogenous hypertriglyceridaemia', 'high density lipoprotein cholesterol level QTL 11', 'familial lipoprotein lipase deficiency (disorder) [ambiguous]', 'Burger-Grutz syndrome', 'Fredrickson type I lipaemia', 'lipoprotein lipase deficiency, familial']",14118,238600,309015,,"['-0.3142', '0.3462', '0.02551', '0.1482', '-0.143', '-0.1599', '-0.2556', '-0.0777', '0.1978', '0.2778', '-0.2041', '-0.3186', '0.4292', '0.411', '-0.6562', '-0.10175', '0.0361', '0.1493', '-0.2457', '-0.3694', '0.04886', '-0.441', '0.1849', '-0.1223', '0.0006742', '0.294', '0.368', '0.10297', '-0.08984', '-0.429', '0.3804', '0.3962', '0.02908', '-0.2423', '-0.2068', '-0.2', '0.0994', '0.262', '0.3572', '-0.3862', '-0.2048', '-0.374', '0.412', '-0.01363', '-0.1487', '-0.3481', '0.35', '-0.2196', '0.2062', '0.2756', '0.10834', '-0.1332', '0.4712', '-0.2705', '-0.2825', '0.05862', '0.04984', '-0.2496', '-0.506', '-0.1603', '0.10657', '0.368', '0.4563', '-0.705', '0.1384', '0.3765', '0.3638', '-0.1407', '-0.5303', '-0.1802', '-0.552', '0.1136', '-0.0544', '0.1226', '0.3545', '0.4263', '0.11743', '0.2563', '-0.006084', '-0.56', '-0.1705', '-0.21', '0.004326', '-0.0866', '0.0241', '0.1985', '0.3682', '0.01012', '0.507', '0.03964', '-0.2145', '0.1617', '-0.4539', '-0.146', '0.714', '0.5527', '0.08307', '-0.6284', '-0.2583', '0.03836']",C84771,,D008072,272.3,,,
mondo:0009388,hyperlysinemia,"['lysine:Alpha-ketoglutarate reductase deficiency', 'hyperlysinemia, type I', 'Alpha-aminoadipic semialdehyde synthase deficiency', 'L-lysine:NAD-oxido-reductase deficiency', 'lysine alpha-ketoglutarate reductase deficiency', 'hyperlysinemia', 'hyperlysinemia (disease)', 'hyperlysinemia, type 1', 'lysine intolerance', 'hyperlysinemia type I', 'L-lysine NAD-oxido-reductase deficiency']",9274,238700,2203,C0268553,"['-0.3499', '0.11005', '-0.3384', '-0.0468', '0.02228', '-0.212', '-0.5684', '0.3713', '-0.1729', '-0.116', '0.03632', '-0.2036', '0.6733', '0.1227', '-0.007275', '-0.2255', '0.3115', '0.359', '-0.3398', '-0.8584', '0.02522', '0.01531', '0.502', '-0.04453', '0.5576', '-0.1274', '-0.1276', '-0.0778', '0.0014715', '-0.1528', '0.3796', '-0.4756', '-0.11035', '0.3716', '-0.6367', '-0.1561', '0.5493', '-0.1475', '0.292', '-0.11774', '0.0848', '-0.0004692', '0.454', '-0.1852', '-0.2566', '-0.601', '0.438', '-0.3413', '0.0618', '-0.01816', '-0.0742', '-0.5747', '-0.0585', '-0.361', '0.2676', '0.508', '0.5376', '-0.10736', '-0.0501', '0.237', '0.2335', '-0.04178', '0.657', '-0.0882', '0.2876', '0.3848', '-0.00782', '0.351', '-0.5415', '0.2256', '-0.272', '0.4092', '-0.0373', '-0.0491', '-0.04938', '0.299', '0.2118', '0.1173', '-0.1166', '0.00738', '0.0777', '0.10754', '0.10834', '0.1212', '0.2161', '0.352', '-0.2219', '-0.02899', '0.3682', '0.4321', '0.1697', '0.3984', '-0.3225', '-0.2228', '0.4353', '0.3298', '0.2448', '-0.687', '0.1204', '-0.318']",C123433,,,270.7,,,0002161
mondo:0009389,hyperlysinemia due to defect in lysine transport into mitochondria,['hyperlysinemia due to defect in lysine TRANSPORT into mitochondria'],,238710,,C1855927,,,,C565499,,,,
mondo:0009390,hyperlysinuria with hyperammonemia,"['hyperlysinemia, periodic', 'hyperlysinuria with hyperammonemia']",,238750,,C0268555,,,,,270.7,,,
mondo:0009391,hypermetabolism due to defect in mitochondria,"['hypermetabolism due to defect in mitochondria', 'hypermetabolism due to uncoupled mitochondrial oxidative phosphorylation 1']",,238800,,C1855926,,,,C565498,,,,
mondo:0009392,"hyperopia, high","['hyperopia, high']",,238950,,,,,,C565497,,,,
mondo:0009393,ornithine translocase deficiency,"['ornithine translocase deficiency', 'hyperornithinemia-hyperammonemia-homocitrullinuria (HHH) syndrome', 'HHHS', 'HHH syndrome', 'hyperornithinemia-hyperammonemia-homocitrullinuria syndrome', 'HHH', 'ornithine carrier deficiency', 'Hhh syndrome', 'triple H syndrome', 'ornithine translocase deficiency syndrome', 'ORNT1 deficiency', 'hyperornithinemia-hyperammonemia-homocitrullinemia syndrome']",0050720,238970,415,C0268540,"['0.0868', '0.0842', '-0.634', '-0.406', '-0.0745', '-0.1029', '-0.3953', '0.7036', '-0.5566', '-0.4114', '-0.3628', '-0.1211', '0.00573', '-0.2588', '-0.2133', '-0.258', '0.0644', '-0.3613', '-0.2532', '-0.5103', '-0.1567', '-0.584', '0.2505', '-0.5024', '-0.2507', '-0.3765', '-0.06287', '0.1835', '0.1505', '-1.143', '0.3333', '-0.0411', '0.804', '0.321', '-0.6304', '-0.0398', '-0.3708', '0.0775', '0.007015', '0.0956', '-0.215', '-0.2317', '-0.004288', '-0.187', '-0.2664', '-0.1538', '-0.5425', '-0.5195', '0.2178', '0.527', '-0.3635', '0.2142', '0.1814', '-0.3525', '0.679', '0.3042', '0.9097', '-0.1766', '-0.0879', '0.4612', '0.2186', '0.5815', '0.777', '-0.349', '-0.196', '0.429', '0.4568', '0.1048', '-0.729', '-0.125', '-0.2191', '0.5664', '-0.2155', '0.006916', '0.0637', '0.3623', '0.845', '-0.244', '-0.1035', '0.09247', '-0.1267', '-0.02747', '-0.6997', '-0.011955', '0.691', '0.983', '0.3396', '0.154', '0.4456', '0.1973', '0.2373', '0.253', '-0.505', '0.1324', '-0.04388', '-0.115', '0.2808', '0.1561', '0.1127', '0.3079']",C129029,,C538380,,,,
mondo:0009394,juvenile Paget disease,"['familial osteoectasia', 'hyperphosphatasemia, chronic congenital idiopathic', 'JPD', 'PDB5', 'hyperostosis corticalis deformans juvenilis', 'JPG', 'Paget disease juvenile type', 'hyperostosid corticalis deformans juvenilis', 'juvenile Pagets disease', 'juvenile Paget disease', 'Paget disease of bone 5, juvenile-onset', 'juvenile Paget^s disease', 'familial hyperphosphatasia', 'osteoectasia, familial', 'hyperphosphatasia, familial idiopathic', 'hereditary hyperphosphatasia']",0081368,239000,2801,,"['0.288', '-0.0619', '0.2788', '0.10205', '0.0771', '-0.1434', '0.11816', '0.756', '-0.784', '-0.00427', '0.1543', '0.162', '-0.12146', '1.1045', '-0.00914', '-0.3047', '0.10187', '0.1292', '-0.638', '-0.05933', '0.593', '-0.303', '-0.2363', '-0.3486', '-0.1349', '-0.0702', '-0.11505', '-0.0658', '0.1301', '0.4797', '-0.1711', '-0.36', '0.103', '0.1367', '0.0623', '-0.2274', '-0.0755', '-0.5933', '0.882', '-0.0998', '0.1893', '0.05624', '0.4634', '-0.1985', '0.5005', '-0.2888', '0.04083', '0.0714', '0.373', '-0.1537', '-0.04446', '-0.2316', '0.8096', '-0.02974', '-0.2306', '-0.4353', '-0.4595', '0.6714', '-0.578', '-0.09686', '0.359', '-0.1045', '-0.1741', '-0.209', '-0.481', '0.428', '-0.03143', '0.6826', '0.0818', '0.6675', '0.2424', '-0.007496', '0.1829', '-0.857', '-0.09186', '0.8145', '-0.4011', '0.789', '-0.1016', '-0.283', '-0.5913', '-0.4', '-0.4688', '0.4783', '-0.489', '0.159', '0.672', '-0.6245', '0.832', '0.61', '0.1603', '-0.397', '-0.713', '0.4167', '0.3545', '0.5527', '0.1833', '-0.0847', '-0.04517', '-0.05832']",C131861,,C537701,,,,
mondo:0009395,hyperostosis corticalis generalisata,"['VAN Buchem disease', 'endosteal hyperostosis', 'hyperphosphatasemia tarda', 'endosteal hyperostosis, autosomal recessive', 'endosteal hyperostosis autosomal recessive', 'van Buchem disease', 'SOST-related sclerosing bone dysplasia', 'van Buchem disease type 1', 'hyperostosis corticalis generalisata', 'Van Buchem disease', 'VBCH']",0080036,239100,3416,,"['-0.4653', '0.232', '0.602', '-0.1488', '0.0756', '-0.06506', '-0.11523', '0.4097', '-0.24', '-0.04288', '-0.488', '-0.03075', '0.04462', '0.1776', '-0.0245', '-0.2036', '0.4338', '-0.0591', '-0.0321', '-0.573', '0.217', '-0.2115', '0.4397', '-0.06805', '0.2366', '0.0648', '-0.0791', '0.0328', '0.2307', '0.2246', '-0.00809', '0.02342', '-0.09753', '0.1832', '0.4246', '-0.4714', '-0.08734', '-0.495', '0.0407', '-0.583', '-0.4019', '-0.3533', '0.1694', '-0.3188', '0.2324', '-0.591', '0.1432', '0.3638', '0.0679', '-0.09424', '0.04263', '0.1362', '-0.1313', '0.1164', '-0.5327', '-0.4424', '0.01063', '0.1857', '-0.286', '0.1054', '0.03372', '-0.0603', '-0.5415', '-0.02531', '-0.07526', '-0.06586', '-0.0752', '0.5757', '-0.02773', '0.4656', '-0.1427', '0.1355', '0.3743', '-0.1552', '-0.3323', '0.2786', '0.0787', '0.1993', '-0.05142', '-0.549', '-0.2479', '-0.11633', '0.2075', '0.371', '-0.1584', '-0.06433', '-0.08875', '0.2224', '0.298', '-0.09625', '-0.1254', '0.0942', '-0.02112', '-0.0545', '0.3645', '0.3425', '0.4658', '-0.2747', '0.2101', '-0.001428']",C131812,,,,,,
mondo:0009396,"hyperparathyroidism, neonatal self-limited primary, with hypercalciuria","['hyperparathyroidism, neonatal self-limited primary, with hypercalciuria']",,239199,,C1855924,,,,C565496,,,,
mondo:0009397,neonatal severe primary hyperparathyroidism,"['neonatal severe hyperparathyroidism', 'hyperparathyroidism, neonatal severe primary', 'NSHPT', 'hyperparathyroidism, neonatal', 'Nsph', 'hyperparathyroidism, neonatal severe']",,239200,417,C1832615,"['0.2979', '-0.3127', '-0.5024', '0.3533', '-0.1925', '0.7393', '-0.3975', '0.6274', '-0.5176', '-0.00495', '0.1134', '-0.0717', '-0.265', '0.557', '-0.5576', '-0.292', '-0.7715', '0.12115', '-0.7236', '-1.031', '0.05463', '-0.6494', '0.574', '-0.3098', '0.4568', '-0.1965', '-0.0445', '-0.5703', '0.2451', '0.1548', '0.404', '0.303', '0.1641', '0.01886', '-0.8013', '-0.4844', '-0.00569', '0.3904', '0.4924', '0.1226', '0.2194', '-0.516', '0.466', '-0.732', '0.5815', '-0.605', '-0.1842', '-0.1667', '0.4446', '-0.03326', '-0.0667', '0.04416', '0.661', '-0.1152', '-0.7573', '0.1448', '-0.683', '0.1285', '-0.2874', '0.01767', '0.311', '0.002325', '-0.386', '0.03787', '-0.4866', '0.4705', '0.1165', '0.9023', '-0.608', '-0.01923', '0.4626', '-0.093', '0.548', '-0.2349', '-0.2499', '0.2842', '-0.1041', '0.864', '0.661', '0.359', '-0.132', '0.02013', '-0.01689', '0.2722', '0.06128', '-0.09216', '0.2332', '-0.3262', '1.002', '0.368', '-0.01121', '0.156', '-0.3784', '-0.4858', '0.8257', '0.0579', '-0.3086', '-0.4146', '-0.07446', '0.1813']",C131853,,C563375,,,,
mondo:0009398,hyperphosphatasia with intellectual disability syndrome 1,"['hyperphosphatasia with mental retardation syndrome 1', 'PIGV hyperphosphatasia-intellectual disability syndrome', 'Mabry syndrome', 'hyperphosphatasia with intellectual disability syndrome type 1', 'hyperphosphatasia with intellectual disability syndrome 1', 'hyperphosphatasia with mental retardation syndrome type 1', 'hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGV', 'HPMRS1', 'glycosylphosphatidylinositol biosynthesis defect 2']",,239300,,CN030519,,,,,,,,
mondo:0009399,"hyperphosphatemia, polyuria, and seizures","['hyperphosphatemia, polyuria, and seizures']",,239350,,C1855922,,,,C565494,,,,
mondo:0009400,hyperprolinemia type 1,"['hyperprolinemia caused by mutation in PRODH', 'PRODH hyperprolinemia', 'HYRPRO1', 'proline oxidase deficiency', 'hyperprolinemia, type 1', 'HPI', 'hyperprolinemia, type I']",0080542,239500,419,,"['-0.1829', '0.3015', '0.1873', '-0.249', '0.02643', '-0.414', '0.03897', '0.1572', '-0.0814', '-0.1384', '-0.2069', '-0.3093', '0.1298', '0.03044', '0.0963', '0.32', '0.01363', '0.03812', '-0.121', '-0.6846', '-0.04358', '-0.2312', '0.6855', '-0.08167', '0.2637', '-0.2688', '0.01758', '-0.2472', '-0.00976', '-0.1588', '0.412', '-0.1239', '0.3264', '0.2727', '-0.5103', '-0.4219', '-0.2118', '-0.1569', '-0.0874', '-0.2668', '0.1439', '-0.657', '0.4001', '-0.1836', '-0.0744', '-0.4363', '0.4204', '-0.0379', '-0.10187', '0.1499', '-0.013794', '0.2593', '-0.3005', '-0.3347', '0.10376', '0.0837', '0.4448', '-0.4097', '-0.515', '0.2783', '0.064', '-0.0954', '0.3848', '-0.1235', '0.199', '-0.0059', '0.2015', '0.0746', '-0.3616', '-0.04745', '-0.4458', '0.03732', '-0.2291', '0.2668', '0.07214', '0.4045', '0.388', '-0.2019', '0.06125', '-0.02997', '0.3677', '0.299', '-0.04092', '0.266', '0.3044', '0.342', '0.003036', '0.2308', '0.3542', '0.2893', '0.2498', '0.5303', '-0.134', '-0.296', '0.3567', '0.587', '0.2664', '-0.2356', '0.172', '0.11896']",,,,270.8,,10058513,
mondo:0009401,hyperprolinemia type 2,"['hyperprolinemia, type 2', '1 alpha pyrroline-5-carboxylate dehydrogenase deficiency', 'hyperprolinemia, type II', 'type 2 hyperprolinemia', 'HPII', 'delta1-pyrroline-5-carboxylate dehydrogenase deficiency', 'hyperprolinemia caused by mutation in ALDH4A1', '1-pyrroline-5-carboxylate dehydrogenase deficiency', 'HYRPRO2', 'ALDH4A1 hyperprolinemia']",0080543,239510,79101,C2931835,"['-0.2546', '0.3577', '0.04456', '-0.3384', '-0.009315', '-0.3215', '-0.1018', '0.225', '-0.2312', '-0.0841', '-0.1859', '-0.07275', '-0.04483', '-0.0656', '0.1884', '0.1499', '-0.014534', '-0.0528', '-0.0302', '-0.672', '-0.06476', '-0.1252', '0.4954', '0.1245', '0.1567', '-0.2062', '0.1505', '-0.10046', '0.0762', '-0.11505', '0.1691', '0.07947', '0.2852', '0.3606', '-0.3572', '-0.1156', '-0.1165', '-0.2898', '-0.1316', '-0.06366', '0.1754', '-0.416', '0.1433', '0.2666', '-0.1722', '-0.3953', '0.3157', '0.03696', '-0.0776', '0.1339', '0.1473', '0.142', '-0.263', '-0.358', '0.01348', '-0.03647', '0.151', '-0.105', '-0.1407', '0.345', '0.07855', '-0.1998', '0.381', '-0.0424', '0.02695', '0.0785', '0.1846', '0.2345', '-0.446', '0.1941', '-0.386', '-0.0493', '-0.07245', '-0.2979', '0.2573', '0.4233', '0.1932', '-0.2184', '-0.08057', '-0.1142', '0.1907', '0.24', '-0.2128', '0.1537', '0.3867', '0.3303', '0.003918', '0.1736', '0.5225', '0.2764', '0.3281', '0.589', '-0.00987', '-0.339', '0.581', '0.4563', '0.2498', '-0.335', '0.1909', '0.1543']",,,C538385,,,10058514,
mondo:0009402,acrofrontofacionasal dysostosis 2,"['acrofrontofacionasal syndrome type 2', 'acrofrontofacionasal dysostosis with genitourinary anomalies', 'Naguib-Richieri-Costa syndrome', 'acrofrontofacionasal dysostosis 2', 'Naguib syndrome', 'hypertelorism-hypospadias-polysyndactyly syndrome', 'acrofrontofacionasal dysostosis type 2', 'AFFN dysostosis 2', 'hypertelorism hypospadias polysyndactyly syndrome', 'hypertelorism, hypospadias, and polysyndactyly syndrome', 'acrofrontofacionasal dysostosis, severe']",,239710,2211,,,,,C538332,,,,
mondo:0009403,hypertelorism and tetralogy of fallot,['hypertelorism and tetralogy of fallot'],,239711,,C1855903,,,,C538386,,,,
mondo:0009404,"hypertelorism, microtia, facial clefting syndrome","['hypertelorism-microtia-facial clefting syndrome', 'Bixler-Christian-Gorlin syndrome', 'Bixler syndrome', 'hypertelorism, microtia, facial clefting syndrome', 'Bixler Christian Gorlin syndrome', 'hypertelorism microtia facial clefting syndrome', 'hypertelorism-microtia-clefting syndrome', 'HMC syndrome']",14670,239800,2213,C0220742,,,,C537632,,,,
mondo:0009405,cervical hypertrichosis-peripheral neuropathy syndrome,"['cervical hypertrichosis peripheral neuropathy', 'hypertrichosis, congenital anterior cervical, with peripheral sensory and motor neuropathy']",,239840,2218,C2931676,,,,C565492,,,,
mondo:0009406,hypertrichotic osteochondrodysplasia Cantu type,"['Craniofaciocardioskeletal syndrome', 'hypertrichotic osteochondrodysplasia (Cantu syndrome)', 'hypertrichotic osteochondrodysplasia', 'Cantu syndrome', 'hypertrichotic osteochondrodysplasia, Cantu type']",0060569,239850,1517,C0795905,"['-0.4587', '0.3086', '0.2375', '-0.3708', '0.508', '-0.4841', '-0.387', '0.649', '-0.391', '0.08386', '-0.1483', '-0.1868', '0.03604', '-0.4954', '-0.4888', '0.324', '0.8223', '-0.05682', '-0.472', '-0.5244', '0.1569', '-0.06192', '0.4402', '-0.676', '0.3108', '-0.1555', '-0.3364', '0.06726', '0.4534', '0.07837', '0.636', '-0.2319', '0.11365', '0.2478', '0.3743', '-0.168', '-0.514', '-0.1134', '-0.006287', '-0.00912', '0.326', '-0.4768', '-0.1359', '-0.1809', '-0.1744', '-0.2717', '0.2305', '0.39', '-0.3252', '-0.4302', '-0.2439', '0.05725', '-0.129', '0.4944', '-0.757', '-0.5225', '-0.209', '-0.3223', '0.1324', '0.1128', '0.3442', '0.1249', '-0.5376', '-0.1622', '-0.183', '-0.241', '0.1766', '0.5044', '-0.3447', '0.6606', '-0.2081', '0.1847', '0.1569', '-0.11554', '-0.604', '0.568', '0.1006', '-0.4607', '-0.1719', '0.1781', '0.4739', '-0.05142', '0.3188', '-0.00208', '0.03845', '0.3088', '-0.3955', '0.4639', '0.1699', '0.3376', '0.1576', '0.6455', '0.2104', '0.3247', '0.9023', '0.2817', '0.3103', '-0.4797', '0.5244', '0.07294']",,,C535572,,,,
mondo:0009407,hypertrophic neuropathy and cataract,['hypertrophic neuropathy and cataract'],,239900,,C1855885,,,,C565490,,,,
mondo:0009408,"hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase","['hyperuricemia, infantile, with abnormal behavior and normal hypoxanthine guanine phosphoribosyltransferase']",,240000,,C1855884,,,,C565489,,,,
mondo:0009409,"hypervitaminosis a, susceptibility to","['hypervitaminosis a, susceptibility to']",,240150,,,,,,,,,,
mondo:0009411,autoimmune polyendocrine syndrome type 1,"['Whitaker syndrom', 'autoimmune hypoparathyroidism-chronic candidiasis-Addison disease syndrome', 'autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy', 'multiple endocrine deficiency-Addison disease-candidiasis syndrome', 'autoimmune polyendocrinopathy caused by mutation in aire', 'autoimmune polyglandular syndrome type 1', 'autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED)', 'autoimmune polyglandular syndrome I', 'polyglandular autoimmune syndrome, type 1', 'polyglandular autoimmune syndrome type 1', 'ham syndrome', 'autoimmune polyendocrinopathy type 1', 'APECED syndrome', 'hypoadrenocorticism with hypoparathyroidism and superficial Moniliasis', 'autoimmune polyendocrine syndrome, type I, with or without reversible metaphyseal dysplasia', 'autoimmune polyendocrinopathy syndrome , type I, with or without reversible metaphyseal dysplasia', 'polyglandular deficiency syndrome, Persian-Jewish type', 'APS type 1', 'autoimmune polyglandular syndrome, type 1', 'autoimmune polyendocrinopathy syndrome type 1', 'MEDAC syndrome', 'APS 1', 'Whitaker syndrome', 'APS1', 'PGA 1', 'autoimmune polyendocrine syndrome type 1', 'AIRE autoimmune polyendocrinopathy', 'autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome', 'aire autoimmune polyendocrinopathy', 'hypoparathyroidism-Addison disease-mucocutaneous candidiasis syndrome', 'autoimmune polyendocrinopathy syndrome, type I, autosomal dominant']",0050167,240300,3453,C0085859,"['0.3738', '0.2056', '-0.2996', '0.02025', '0.2676', '-0.3384', '0.0935', '0.1527', '-0.9336', '-0.575', '-0.1455', '0.1686', '-0.2278', '0.277', '-0.10394', '0.02419', '0.02472', '-0.1185', '-0.0974', '-0.6924', '0.08295', '-0.8013', '0.61', '-0.1871', '-0.2284', '0.1691', '-0.744', '-0.3894', '0.2751', '-1.073', '0.907', '-0.145', '-0.2068', '0.6177', '0.1736', '-0.3975', '-0.4097', '0.2522', '-0.672', '0.3315', '-0.525', '0.7363', '0.5166', '-0.3462', '0.0255', '0.03406', '0.1658', '-0.04025', '0.2944', '-0.3757', '-0.1716', '0.5083', '0.513', '-0.0739', '-0.7896', '0.1174', '0.4536', '-0.617', '-0.2727', '0.1367', '0.2847', '0.561', '0.5454', '0.0964', '0.7515', '0.5107', '0.397', '0.451', '-0.2856', '0.2268', '-0.1736', '-0.618', '0.3823', '-0.01298', '0.1613', '-0.1241', '0.4128', '0.10004', '0.273', '-0.2262', '0.03256', '-0.1113', '-0.4739', '-0.4644', '-0.4072', '0.2189', '0.1002', '0.02092', '0.2617', '0.07837', '-0.2341', '-0.0936', '0.343', '-0.5986', '0.7075', '0.0877', '0.5938', '-0.2106', '0.4265', '-0.1936']",C129727,,,258.8,,,
mondo:0009412,scurvy,"['L-gulonolactone oxidase, nonfunctional', 'scurvy', 'hypoascorbemia', 'vitamin C deficiency', 'vitamin C, inability to synthesise', 'ascorbic acid deficiency', 'L-gulonolactone oxidase pseudogene', 'vitamin C, inability to synthesize', 'deficiency of vitamin C', 'Gulo, nonfunctional', 'scorbutus']",13724,240400,,C0036474,,C35010,1001169,D012614,267,E54,10047623,
mondo:0009413,"immunodeficiency, common variable, 2","['CVID2', 'hypogammaglobulinemia due to TACI deficiency', 'immunodeficiency, common variable, 2', 'antibody deficiency due to TACI defect', 'immunodeficiency, common variable, type 2']",0081145,240500,,C3150354,,,,,,,,
mondo:0009414,glycogen storage disorder due to hepatic glycogen synthase deficiency,"['GSD0A', 'liver glycogen storage disease 0', 'liver GSD 0', 'glycogen storage disease type 0, liver', 'glycogen storage disease due to glycogen synthase deficiency of liver', 'GSD type 0a', 'glycogen storage disease due to liver glycogen synthase deficiency', 'glycogenosis type 0a', 'GSD 0A', 'liver glycogen storage disease due to glycogen synthase deficiency', 'liver glycogen synthase deficiency', 'glycogen storage disease 0, liver', 'hepatic glycogen synthase deficiency', 'glycogen storage disease type 0a', 'GSD due to hepatic glycogen synthase deficiency', 'hypoglycemia with deficiency of glycogen synthetase in the liver']",,240600,2089,C1855861,"['0.09735', '0.0845', '-0.5884', '0.1758', '0.193', '-0.275', '-0.1346', '0.5923', '-0.1096', '-0.10114', '-0.1877', '-0.001891', '0.0717', '0.06104', '-0.6777', '0.0842', '-0.1688', '-0.2339', '-0.5713', '-0.3718', '0.3794', '-0.513', '0.5645', '0.123', '-0.582', '0.373', '-0.0685', '-0.3782', '0.1869', '0.1301', '0.283', '0.06305', '0.3193', '0.6074', '-0.1096', '-0.45', '-0.04654', '-0.1299', '-0.3186', '-0.163', '-0.2793', '-0.5327', '0.117', '0.337', '-0.3347', '0.3364', '0.2252', '0.1864', '-0.5317', '1.039', '-0.03592', '-0.2103', '0.03583', '0.0975', '0.224', '-0.5815', '0.1043', '-0.0254', '-0.1862', '-0.1043', '0.6445', '0.1472', '0.531', '-0.4827', '-0.5273', '0.1371', '0.12036', '0.06198', '-0.2925', '0.0964', '-0.4626', '-0.03412', '0.309', '0.587', '0.7305', '0.7134', '-0.0762', '0.03415', '-0.563', '0.3994', '-0.1366', '-0.1046', '0.1941', '0.236', '0.7837', '0.1175', '-0.11945', '0.1431', '0.984', '-0.1243', '1.055', '0.05505', '0.1224', '0.1338', '0.5107', '0.5747', '-0.1156', '-0.8594', '0.0655', '0.0773']",,,C565485,,,,
mondo:0009415,"hypoglycemia, leucine-induced","['LIH', 'leucine-sensitive hypoglycemia of infancy', 'hypoglycemia leucine induced', 'familial infantile hypoglycemia precipitated by leucine', 'hypoglycemia leucine-induced', 'hypoglycemia of infancy, leucine-sensitive', 'hypoglycemia, leucine-induced']",0112262,240800,,C0271714,"['0.391', '0.1925', '0.0306', '0.7754', '-0.521', '-0.06616', '0.03928', '0.887', '0.1316', '-0.1332', '0.1469', '-0.075', '0.1389', '1.255', '-0.778', '-0.10645', '-0.2258', '0.0798', '-0.5493', '-0.14', '-0.1956', '-0.3088', '-0.2186', '0.268', '-0.8364', '-0.8154', '-0.576', '-0.772', '0.2076', '-0.395', '0.645', '0.1614', '-0.0455', '0.163', '-0.641', '0.5156', '-0.5967', '0.3574', '0.1304', '-0.541', '0.1847', '-0.2302', '-0.3901', '0.3218', '-0.0305', '-0.4143', '0.1125', '-0.132', '-0.1097', '0.69', '0.4612', '0.4954', '0.4426', '0.3733', '-0.3406', '0.2045', '-0.1373', '0.08435', '-1.0625', '0.4558', '-0.3132', '0.539', '0.2273', '-0.7935', '-0.663', '-0.04297', '0.05707', '0.312', '-0.945', '0.1344', '0.2874', '0.6235', '0.1477', '-0.839', '0.0406', '0.7983', '-0.1338', '0.4175', '-0.0958', '0.0643', '-0.2917', '0.4333', '-0.788', '0.2805', '0.1853', '-0.0977', '-0.3384', '-0.2693', '1.146', '0.1796', '0.2822', '-0.1569', '0.1299', '0.1467', '0.818', '0.3992', '-0.269', '-0.8374', '-0.11566', '0.995']",,0006856,C537150,,,,
mondo:0009416,hypoinsulinemic hypoglycemia and body hemihypertrophy,"['hypoinsulinemic hypoglycemia with hemihypertrophy', 'HIHGHH']",0112263,240900,293964,CN203155,"['0.38', '0.0807', '0.1001', '0.8237', '-0.547', '0.0159', '-0.02855', '0.8115', '-0.004272', '-0.095', '0.1892', '-0.001619', '0.2605', '1.261', '-0.7896', '-0.09436', '-0.3767', '0.1726', '-0.5566', '0.01548', '-0.1188', '-0.3157', '-0.364', '0.1398', '-0.635', '-0.7466', '-0.546', '-0.917', '0.1621', '-0.568', '0.648', '0.293', '-0.08246', '0.02373', '-0.688', '0.521', '-0.5063', '0.3972', '-0.00818', '-0.3403', '0.3179', '-0.244', '-0.517', '0.1498', '0.0644', '-0.47', '-0.077', '-0.1459', '-0.02605', '0.6235', '0.5195', '0.4172', '0.5576', '0.169', '-0.3054', '0.3064', '-0.1904', '0.004795', '-1.055', '0.612', '-0.209', '0.5083', '0.29', '-0.78', '-0.8047', '0.0711', '0.3586', '0.2517', '-0.8047', '0.1881', '0.2009', '0.6587', '0.238', '-0.4836', '-0.0956', '0.6587', '-0.1464', '0.652', '-0.2401', '0.04446', '-0.2301', '0.4966', '-0.669', '0.3098', '0.1948', '-0.00758', '-0.2817', '-0.2986', '1.383', '0.223', '0.337', '0.04907', '0.2115', '0.1941', '0.9126', '0.2588', '-0.1151', '-0.785', '-0.1144', '0.8276']",,,,,,,
mondo:0009417,hypergonadotropic hypogonadism-cataract syndrome,"['hypogonadism-cataract syndrome', 'cataracts and testicular failure', 'Lubinsky syndrome', 'hypogonadism cataract syndrome']",,240950,2410,C1855859,,,,C543092,,,,
mondo:0009418,hypogonadism with low-grade mental deficiency and microcephaly,['hypogonadism with low-grade mental deficiency and microcephaly'],,241000,,C1855858,,,,C565482,,,,
mondo:0009419,Woodhouse-Sakati syndrome,"['hypogonadism, alopecia, diabetes mellitus, intellectual disability, deafness, and extrapyramidal syndrome', 'hypogonadism, alopecia, diabetes mellitus, mental retardation, deafness, and extrapyramidal syndrome', 'diabetes-hypogonadism-deafness-intellectual disability syndrome', 'extrapyramidal disorder, progressive, with primary hypogonadism, intellectual disability, and alopecia', 'hypogonadism, diabetes mellitus, alopecia, intellectual disability, and electrocardiographic abnormalities', 'hypogonadism, diabetes mellitus, alopecia, mental retardation, and electrocardiographic abnormalities', 'woodhouse-Sakati syndrome', 'woodhouse Sakati syndrome', 'extrapyramidal disorder, progressive, with primary hypogonadism, mental retardation, and alopecia']",0112264,241080,3464,C0342286,"['-0.1737', '0.9634', '-0.1942', '-0.2554', '0.3315', '-0.6553', '0.09576', '0.512', '-0.1582', '-0.05927', '-0.3835', '-0.1908', '0.274', '-0.359', '-0.1602', '0.4775', '0.4866', '-0.03647', '0.0402', '0.02429', '-0.03647', '-0.4207', '-0.2382', '0.338', '0.2443', '0.1958', '-0.0978', '-0.06415', '0.08905', '-0.498', '0.4568', '0.0867', '0.6274', '-0.1343', '0.3806', '-0.3164', '-0.26', '-0.6416', '-0.2534', '-0.372', '-0.153', '0.4016', '-0.1268', '0.4226', '0.3284', '-0.6675', '-0.0635', '0.4626', '-0.705', '-0.512', '-0.58', '0.3916', '-0.3333', '0.0804', '0.3882', '-0.4153', '0.604', '-0.6733', '-0.05362', '0.012405', '0.0436', '0.002544', '0.37', '-0.12225', '-0.531', '0.3384', '0.1498', '0.6406', '-0.5513', '0.338', '-0.5146', '0.4453', '0.0967', '0.2722', '-0.1974', '0.265', '0.2603', '0.3357', '0.03604', '0.154', '0.323', '-0.08075', '0.1028', '0.595', '0.2413', '0.3386', '0.2236', '0.778', '-0.1382', '0.775', '-0.02452', '0.0941', '0.593', '-0.0001634', '0.879', '-0.1522', '0.3516', '-0.4827', '-0.0996', '-0.291']",,,C536742,759.89,,,
mondo:0009420,primary hypergonadotropic hypogonadism-partial alopecia syndrome,"['hypergonadotropic hypogonadism and partial alopecia', 'Al Awadi-Farag-Teebi syndrome']",,241090,2232,,,,,C567109,,E28.3,,
mondo:0009421,"hypogonadism, male","['hypogonadism and testicular atrophy', 'hypogonadism, male']",,241100,,,,,,,257.2,,,
mondo:0009422,hypohidrosis with abnormal palmar dermal Ridges,"['sweat gland hypoplasia', 'hypohidrosis with abnormal palmar dermal Ridges']",,241120,,C1855856,,,,C565481,,,,
mondo:0009423,"hypokalemic alkalosis, familial, with specific renal tubulopathy","['hypokalemic alkalosis, familial, with specific renal tubulopathy', 'hypokalemia, familial', 'Gullner syndrome']",,241150,,C0268444,,,,C562654,,,,
mondo:0009424,Bartter disease type 2,"['hypokalemic alkalosis with hypercalciuria antenatal 2', 'hyperprostaglandin E syndrome 2', 'Bartter syndrome type 2 antenatal', 'Bartter syndrome type 2', 'Bartter syndrome, type 2, antenatal', 'Bartter syndrome antenatal type 2', 'BARTS2', 'hypokalemic alkalosis with hypercalciuria 2, antenatal', 'Bartter syndrome, type 2', 'hypokalemic alkalosis with hypercalciuria 2 antenatal', 'Bartter syndrome caused by mutation in KCNJ1', 'KCNJ1 Bartter syndrome', 'hypokalemic alkalosis with hypercalciuria, antenatal, 2', 'Bartter syndrome, antenatal, type 2']",0110143,241200,93604,,"['-0.05286', '0.4907', '-0.2935', '-0.1147', '-0.2069', '-0.4983', '-0.03113', '0.8525', '-0.2947', '-0.2664', '-0.4697', '-0.249', '0.2776', '0.2742', '-0.2052', '-0.316', '0.2065', '0.303', '0.795', '-0.732', '-0.277', '-0.3135', '0.7856', '-0.1378', '0.3262', '0.4368', '0.07227', '0.1542', '0.0853', '0.2255', '0.4539', '-0.1329', '0.546', '0.773', '-0.2089', '0.1965', '-0.004143', '0.2341', '-0.3984', '-0.1266', '-0.448', '-0.11914', '0.4275', '-0.337', '0.10583', '0.257', '-0.3342', '0.3994', '0.0346', '0.006573', '0.1571', '-0.3135', '0.04797', '-0.7646', '-0.3345', '0.438', '0.1866', '-0.643', '0.381', '0.732', '0.2554', '0.04587', '0.1088', '-0.2744', '-0.2174', '-0.3376', '0.2394', '0.2394', '-0.5503', '0.8105', '0.0777', '-0.07306', '0.4133', '-0.3203', '0.1142', '-0.000344', '-0.1316', '0.00245', '-0.4592', '-0.1516', '-0.04675', '0.3323', '-0.2922', '-0.4297', '-0.0175', '0.3728', '-0.01614', '0.0422', '0.6187', '-0.2161', '0.7246', '-0.02515', '-0.05258', '-0.2482', '0.4526', '0.304', '0.1234', '-0.7246', '-0.2467', '-0.02211']",,,C537651,,,,
mondo:0009425,hypomandibular faciocranial dysostosis,['hypomandibular faciocranial dysostosis'],,241310,1790,,,,,C537154,,,,
mondo:0009426,hypoparathyroidism-retardation-dysmorphism syndrome,"['HRD syndrome', 'hypoparathyroidism-intellectual disability-dysmorphism syndrome', 'Sanjad-Sakati syndrome', 'HRDS', 'hypoparathyroidism with short stature, mental retardation, and seizures', 'hypoparathyroidism with short stature, intellectual disability, and seizures', 'HRD', 'hypoparathyroidism-retardation-dysmorphism syndrome', 'hypoparathyroidism-short stature-intellectual disability-seizures syndrome', 'hypoparathyroidism with short stature, intellectual disability and seizures', 'SSS', 'hypoparathyroidism, congenital, associated with Dysmorphism, Growth retardation, and developmental delay', 'hypoparathyroidism, congenital, associated with dysmorphism, growth retardation and developmental delay', 'hypoparathyroidism with short stature, mental retardation and seizures', 'Richardson-Kirk syndrome']",0060348,241410,2323,C1855840,"['-0.529', '-0.1821', '-0.304', '-0.5947', '-0.4775', '0.6924', '-0.4187', '0.72', '-1.298', '-1.152', '-0.1918', '-0.07666', '0.1586', '0.5366', '-0.6772', '0.563', '0.29', '-0.6567', '0.12463', '-0.4575', '0.3718', '-0.3203', '-0.3447', '-0.2335', '-0.003712', '0.1384', '-0.3713', '-0.2456', '0.8853', '-0.7935', '-0.04752', '0.11536', '-0.2257', '-0.1376', '-0.158', '-0.4243', '0.11414', '0.0516', '0.4795', '0.1265', '0.4324', '-0.2954', '0.5405', '-0.6543', '0.4194', '-0.1683', '0.892', '0.5967', '-0.1071', '-0.0484', '0.1826', '0.2163', '0.612', '-0.2637', '-0.784', '-0.8833', '-0.1512', '-0.604', '-0.06586', '-0.2512', '-0.3977', '-0.2428', '-0.0748', '-0.11115', '-0.1134', '0.6455', '-0.02518', '0.898', '-0.6143', '0.3633', '-0.4358', '-0.1185', '0.4065', '-0.01291', '0.0702', '0.82', '0.3198', '-0.3325', '0.1886', '0.7017', '0.2852', '0.504', '-0.174', '-0.5127', '-0.04477', '-0.5645', '-0.06165', '0.219', '0.3184', '0.3643', '-0.2532', '0.9736', '-0.00742', '-0.1197', '0.007202', '0.1423', '0.3677', '-0.9536', '0.1422', '0.10736']",C133727,,C537157,,,,
mondo:0009429,"hypophosphatemia, renal, with intracerebral calcifications","['hypophosphatemia, renal, with intracerebral calcifications']",,241519,,C1855809,,,,C565478,,,,
mondo:0009430,"hypophosphatemic rickets, autosomal recessive, 1","['Arhr', 'ARHR1', 'hypophosphatemia, autosomal recessive', 'DMP1 autosomal recessive hypophosphatemic rickets', 'hypophosphatemic rickets, AR', 'hypophosphatemic rickets, autosomal recessive, 1', 'hypophosphatemic rickets, autosomal recessive, type 1', 'autosomal recessive hypophosphatemic rickets caused by mutation in DMP1']",,241520,,C0342643,,,,C562792,,,,
mondo:0009431,hereditary hypophosphatemic rickets with hypercalciuria,"['hypercalciuric rickets', 'hypophosphatemic rickets with hypercalciuria', 'hypophosphatemic rickets with hypercalciuria, hereditary', 'hypophosphatemic hypercalciuric rickets', 'HHRH', 'hypercalciuric hypophosphatemic rickets']",0050947,241530,157215,C1853271,"['0.3506', '-0.05838', '0.425', '-0.235', '-0.0618', '-0.04965', '-0.997', '1.348', '-0.253', '-0.02841', '0.5386', '0.8394', '-0.6973', '0.7505', '-0.5464', '-0.1929', '-0.2433', '0.10626', '-0.6543', '-1.169', '-0.11975', '-0.9673', '0.5', '-0.3586', '0.2412', '-0.4946', '0.0876', '-0.7134', '0.076', '-0.0643', '0.1533', '-0.421', '-0.2678', '0.1072', '-0.03287', '-0.1849', '-0.181', '0.0336', '0.574', '0.2229', '-0.3914', '-0.4016', '-0.459', '-0.1798', '0.2373', '-0.2097', '0.6597', '0.2585', '0.04898', '0.4373', '-0.2367', '-0.5874', '0.3105', '0.2656', '-0.5195', '-0.3665', '0.0281', '0.0284', '-1.103', '0.1153', '0.6265', '-0.2006', '-0.2876', '0.519', '0.3306', '0.6562', '0.7256', '1.202', '-0.77', '-0.666', '0.56', '0.02487', '0.4587', '-0.566', '0.05286', '1.264', '0.0433', '-0.805', '0.15', '0.4365', '0.268', '0.3887', '0.3804', '0.04294', '-0.2062', '-0.09625', '0.253', '0.393', '0.615', '0.2212', '0.5645', '-0.1628', '-0.5273', '0.1615', '-0.5435', '0.1825', '0.55', '-0.42', '-0.5723', '-0.1451']",C131450,,C562793,,E83.3,,
mondo:0009432,"hypopituitarism, congenital, with central diabetes insipidus","['hypopituitarism, congenital, with central diabetes insipidus']",,241540,,C1855800,,,,C565477,,,,
mondo:0009433,hypoplastic left heart syndrome 1,"['GJA1 hypoplastic left heart syndrome', 'hypoplastic left heart syndrome type 1', 'hypoplastic left heart syndrome 1', 'HLHS', 'hypoplastic left heart syndrome caused by mutation in GJA1', 'HLHS1']",,241550,,CN031062,,,,,,,,
mondo:0009434,"hypoproteinemia, hypercatabolic","['Beta-2-microglobulin deficiency', 'B2M deficiency', 'hypoproteinemia, hypercatabolic', 'immunodeficiency 43', 'IMD43']",0111981,241600,,C1855796,,,,C565476,,,,
mondo:0009435,"hypospadias-intellectual disability, Goldblatt type syndrome","['hypospadias intellectual deficit Goldblatt type', 'hypospadias mental retardation Goldblatt type', 'hypospadias-intellectual disability syndrome', 'Goldblatt-Wallis syndrome', 'Goldblatt Wallis syndrome', 'hypospadias intellectual disability syndrome', 'hypospadias intellectual disability Goldblatt type', 'hypospadias-mental retardation syndrome', 'hypospadias mental retardation syndrome']",,241760,2261,,,,,C563067,,,,
mondo:0009436,congenital hypothalamic hamartoma syndrome,"['congenital hypothalamic hamartoma syndrome', 'hamartoma of hypothalamus', 'hypothalamic hamartomas', 'hamartoma of the hypothalamus', 'hypothalamic hamartoma', 'Pallister-Hall-like syndrome']",,241800,2113,,,C4385,,C537158,759.6,,,
mondo:0009437,Bamforth-Lazarus syndrome,"['hypothyroidism, thyroidal or ATHYROIDAL, with spiky hair and cleft palate', 'Bamforth syndrome', 'Bamforth-Lazarus syndrome', 'Athyroidal hypothyroidism-spiky hair-cleft palate syndrome', 'hypothyroidism-cleft palate syndrome', 'hypothyroidism, ATHYROIDAL, with spiky hair and cleft palate', 'hypothyroidism cleft palate hypothyroidism, athyroidal, with spiky hair and cleft palate']",0050655,241850,1226,,"['0.04813', '0.1333', '-0.0752', '0.2115', '0.1332', '0.2986', '-0.195', '0.286', '-0.5635', '-0.7056', '0.0221', '-0.1542', '0.063', '-0.0749', '-0.326', '0.4136', '0.2937', '-0.328', '-0.4797', '-1.266', '0.03198', '-0.561', '0.3943', '-0.6533', '-0.11426', '0.1299', '-0.4873', '0.4976', '1.317', '-0.5537', '0.4111', '0.04645', '0.07526', '-0.09534', '-0.6094', '0.08716', '0.1641', '-0.10266', '-0.04538', '0.335', '0.4033', '0.2463', '0.6733', '-0.4224', '-0.1782', '-0.0736', '0.3665', '0.0373', '-0.1044', '-0.427', '-0.521', '-0.566', '0.2325', '0.1838', '-0.3733', '-0.10376', '0.5923', '-0.481', '-0.2073', '0.4033', '0.5547', '0.7866', '-0.0506', '-0.1871', '-0.5083', '0.1145', '0.8496', '-0.3613', '-0.402', '0.4998', '-0.527', '0.543', '0.3423', '-0.143', '0.06946', '0.1462', '0.604', '-0.5464', '-0.7515', '0.5933', '0.2957', '0.1615', '-0.1147', '0.2258', '-0.1404', '1.061', '0.2229', '0.956', '0.2913', '0.1925', '-0.01491', '0.4053', '0.1786', '-0.2284', '1.487', '-0.3347', '-0.8013', '-0.2164', '0.8643', '-0.609']",,,C537901,,,,
mondo:0009438,"hypouricemia, hypercalcinuria, and decreased bone density","['hypouricemia, hypercalcinuria, and decreased bone density']",,242050,,C1855793,,,,C565475,,,,
mondo:0009439,autosomal recessive congenital ichthyosis 2,"['ichthyosiform erythroderma, Brocq congenital, nonbullous form', 'Brocq congenital ichthyosiform erythroderma nonbullous form', 'NCIE', 'ARCI2', 'ichthyosiform erythroderma, nonbullous congenital, 1, formerly', 'ichthyosis, congenital, autosomal recessive type 2', 'autosomal recessive congenital ichthyosis type 2', 'collodion baby, self-healing', 'ichthyosiform erythroderma, congenital, nonbullous, 1', 'ichthyosiform erythroderma, Brocq congenital, nonbullous form, formerly', 'ichthyosis, congenital, autosomal recessive 2', 'nonbullous congenital ichthyosiform erythroderma 1', 'NBCIE', 'NCIE1', 'ichthyosiform erythroderma, nonbullous congenital, 1']",0060710,242100,,,,C132827,,,,,,
mondo:0014487,congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome,"['SIFD', 'sideroblastic anaemia with B-cell immunodeficiency, periodic fevers, and developmental delay', 'sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay', 'SIFD syndrome']",0080209,616084,369861,C4015172,"['-0.5386', '0.436', '-0.161', '0.2213', '0.5557', '0.1677', '-0.409', '0.5874', '-0.2496', '-0.3542', '0.4658', '-0.02032', '0.4363', '0.2217', '-1.204', '-0.1841', '-0.724', '0.006344', '-0.4976', '-0.636', '-0.02026', '-0.584', '0.248', '-0.3142', '0.704', '-0.375', '-0.3044', '-0.5757', '0.646', '-0.153', '0.1869', '0.4836', '0.497', '0.645', '0.3481', '-0.1277', '-0.92', '-0.4778', '0.303', '-0.1189', '-0.652', '0.2725', '-0.164', '-0.6284', '-0.5757', '-0.7734', '-0.01161', '0.0353', '0.2327', '-0.2245', '0.3835', '0.3755', '0.772', '-0.1389', '0.709', '-0.4004', '-0.1455', '0.1284', '-0.966', '0.1448', '-0.0533', '0.4673', '-0.331', '-0.1255', '0.1289', '0.1669', '0.1855', '0.936', '-0.538', '1.052', '0.938', '-0.362', '-0.5605', '-0.6353', '0.2083', '0.82', '0.3987', '0.1936', '0.11835', '0.3643', '0.2186', '0.07275', '0.1117', '0.2196', '0.3723', '-0.1727', '-0.4543', '0.2128', '0.7207', '-0.2368', '1.05', '0.4307', '-0.221', '-0.224', '0.5454', '0.8237', '0.1643', '0.10925', '0.3823', '-0.3943']",,,,,,,
mondo:0014488,"diabetes mellitus, noninsulin-dependent, 5","['NIDDM5', 'diabetes mellitus, noninsulin-dependent, 5', 'TBC1D4 type 2 diabetes mellitus', 'type 2 diabetes mellitus caused by mutation in TBC1D4', 'diabetes mellitus, noninsulin-dependent, type 5']",,616087,,C4015183,,,,,,,,
mondo:0014489,limb-girdle muscular dystrophy due to POMK deficiency,"['MDDGC12', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 12', 'muscular dystrophy-dystroglycanopathy, limb-girdle, POMK-related', 'LGMD due to POMK deficiency']",0112381,616094,445110,C4015184,,,,,,,,
mondo:0014490,ketoacidosis due to monocarboxylate transporter-1 deficiency,"['MCT1D', 'monocarboxylate transporter 1 deficiency']",,616095,438075,C4015186,,,,,,,,
mondo:0014491,immunodeficiency 37,"['immunodeficiency 37', 'primary immunodeficiency disease caused by mutation in BCL10', 'BCL10 primary immunodeficiency disease', 'combined immunodeficiency due to BCL10 deficiency', 'immunodeficiency type 37', 'IMD37']",0111939,616098,,C4015195,,,,,,,,
mondo:0014492,wooly hair-palmoplantar keratoderma syndrome,"['palmoplantar keratoderma and woolly hair', 'palmoplantar keratoderma and wooly hair', 'woolly hair-palmoplantar hyperkeratosis syndrome', 'keratoderma with wooly hair type IV', 'KWWH type IV', 'PPKWH', 'wooly hair-palmoplantar hyperkeratosis syndrome', 'keratoderma with woolly hair type IV']",,616099,420686,C4015202,,,,,,,,
mondo:0014493,autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency,"['autoimmune lymphoproliferative syndrome, type V', 'ALPS due to CTLA4 haploinsuffiency', 'ALPS type V', 'ALPS type 5', 'CTLA4 haploinsufficiency with autoimmune infiltration', 'CTLA4 haploinsufficiency', 'autoimmune lymphoproliferative syndrome, type 5', 'immune dysregulation with autoimmunity, immunodeficiency, and lymphoproliferation', 'autoimmune lymphoproliferative syndrome type V', 'chai', 'ALPS5', 'CTLA-4 haploinsufficiency with autoimmune infiltration disease', 'autoimmune lymphoproliferative syndrome type 5']",,616100,436159,C4015214,,C126341,,,,,,
mondo:0014494,"psoriasis 15, pustular, susceptibility to","['generalized pustular psoriasis caused by mutation in AP1S3', 'AP1S3 generalized pustular psoriasis', 'psoriasis 15, pustular, susceptibility to', 'susceptibility to pustular psoriasis 15', 'generalised pustular psoriasis caused by mutation in AP1S3', 'PSORS15', 'AP1S3 generalised pustular psoriasis']",0111281,616106,,,,,,,,,,
mondo:0014495,retinitis pigmentosa-juvenile cataract-short stature-intellectual disability syndrome,"['retinal dystrophy-juvenile cataract-short stature syndrome', 'retinal dystrophy, juvenile cataracts, and short stature syndrome', 'RDJCSS']",,616108,436245,C4015242,,,,,,,,
mondo:0014496,mitochondrial complex III deficiency nuclear type 9,"['mitochondrial Complex 3 deficiency, nuclear type 9', 'UQCC3 mitochondrial complex III deficiency', 'MC3DN9', 'mitochondrial complex III deficiency caused by mutation in UQCC3', 'mitochondrial complex III deficiency, nuclear type 9']",0080118,616111,,C4015253,,,,,,,,
mondo:0014497,polyendocrine-polyneuropathy syndrome,"['PEPNS', 'polyendocrine-polyneuropathy syndrome']",,616113,453533,C4015261,"['-0.002365', '0.03546', '-0.001054', '-0.00704', '0.00604', '-0.0448', '0.003794', '0.042', '-0.04034', '-0.02203', '-0.01131', '-0.006985', '-0.007904', '-0.006077', '-0.003443', '-0.01852', '0.00983', '-0.01888', '-0.01046', '-0.0577', '0.000897', '-0.00993', '0.02017', '-0.01646', '0.0138', '-0.003016', '-0.00803', '-0.00825', '0.0319', '-0.01587', '0.0356', '0.0001317', '0.03226', '0.0175', '0.0003443', '-0.00361', '-0.014435', '-0.0096', '-0.01061', '-0.03784', '0.011696', '-0.0222', '0.003212', '-0.0181', '-0.005707', '-0.02606', '-0.011', '0.03604', '0.00854', '0.0077', '-0.01124', '-0.0004447', '-0.007195', '-0.01631', '-0.02084', '-0.01309', '0.02045', '-0.012146', '-0.03848', '0.004658', '0.02423', '0.0105', '-0.0069', '-0.010315', '0.001502', '-0.01159', '0.03123', '0.01006', '-0.0384', '0.04614', '-0.03906', '0.013275', '-0.00889', '-0.02136', '0.02498', '0.01878', '0.00899', '-0.001963', '-0.026', '-0.01602', '0.006126', '0.0009217', '-0.00653', '0.02298', '0.001133', '-0.01123', '0.003864', '0.03305', '0.03488', '0.01427', '0.01955', '0.0388', '0.01174', '0.003124', '0.05475', '0.02014', '0.0357', '-0.03967', '0.00841', '0.001686']",,,,,,,
mondo:0014498,familial cold autoinflammatory syndrome 4,"['familial cold autoinflammatory syndrome type 4', 'familial cold autoinflammatory syndrome caused by mutation in NLRC4', 'familial cold autoinflammatory syndrome 4', 'FCAS4', 'NLRC4 familial cold autoinflammatory syndrome', 'NLRC4-related familial cold autoinflammatory syndrome']",0090065,616115,576349,C4015276,,,,,,,,
mondo:0014499,"intellectual disability, autosomal recessive 46","['NDST1 autosomal recessive non-syndromic intellectual disability', 'intellectual disability, autosomal recessive 46', 'MRT46', 'intellectual disability, autosomal recessive type 46', 'mental retardation, autosomal recessive type 46', 'mental retardation, autosomal recessive 46', 'autosomal recessive non-syndromic intellectual disability caused by mutation in NDST1']",0081210,616116,,C4015283,,,,,,,,
mondo:0014500,atrial conduction disease,"['CCDD', 'CARDIAC conduction disease with or without dilated cardiomyopathy', 'familial atrial tachyarrhythmia-infra-Hisian cardiac conduction disease']",,616117,436242,C4015285,"['-0.1267', '0.2224', '0.07263', '0.08856', '-0.00802', '-0.2573', '0.4377', '0.309', '-0.1306', '0.1125', '-0.2073', '-0.1528', '-0.316', '-0.1305', '-0.07336', '-0.3171', '-0.4312', '-0.2487', '-0.1365', '-0.407', '0.3394', '0.236', '0.2462', '0.002308', '0.02634', '-0.2471', '0.2534', '0.1284', '0.2773', '0.11957', '0.3464', '0.366', '0.391', '0.2668', '-0.01622', '-0.52', '0.12494', '-0.005157', '0.04684', '-0.4106', '0.1401', '-0.02391', '0.3171', '0.1818', '0.01562', '-0.07104', '-0.1708', '0.4922', '-0.2012', '0.3252', '-0.06235', '0.2937', '-0.2156', '-0.0491', '-0.0662', '-0.1975', '0.2664', '0.00551', '-0.2396', '0.03055', '0.1316', '0.1653', '0.2415', '-0.2051', '0.0331', '-0.1327', '0.567', '0.6743', '-0.2927', '0.0792', '-0.3127', '0.0678', '0.2646', '-0.0737', '0.00815', '-0.10297', '0.0646', '0.1296', '-0.2507', '-0.2878', '0.1674', '-0.00909', '0.217', '0.1274', '0.3672', '-0.2499', '0.3264', '-0.0543', '0.054', '0.03223', '0.1649', '0.1829', '0.0857', '0.02094', '0.7114', '0.0905', '0.602', '-0.1531', '-0.4438', '0.1904']",,0005304,,,,,
mondo:0014501,"macular degeneration, early-onset","['macular degeneration, early-onset', 'EOMD']",,616118,,C4015286,,,,,,,,
mondo:0014502,Mendelian susceptibility to mycobacterial diseases due to complete ISG15 deficiency,"['ISG15 deficiency, autosomal recessive', 'ISG15 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency', 'immunodeficiency 38 with basal ganglia calcification', 'IMD38', 'immunodeficiency 38, Mycobacteriosis, autosomal recessive', 'MSMD due to complete ISG15 deficiency', 'immunodeficiency 38']",0111934,616126,319563,C4015293,"['0.2942', '0.1517', '0.02715', '-0.1445', '0.2534', '-0.42', '0.474', '-0.1431', '0.4282', '-0.343', '0.304', '0.0409', '-0.1724', '0.2274', '0.4211', '-0.2075', '0.3276', '-0.1525', '-0.306', '-0.435', '-0.1895', '-0.02461', '0.5435', '-0.4875', '-0.3286', '-0.04892', '-0.678', '0.2847', '0.03333', '-0.786', '-0.1265', '0.137', '0.524', '0.1061', '0.2467', '-0.6494', '-0.3054', '-0.4482', '-0.3704', '0.01343', '0.2773', '-0.49', '0.2205', '-0.453', '-0.1797', '0.0831', '0.03308', '-0.1869', '-0.1294', '0.09796', '0.02226', '-0.6333', '0.4324', '0.0751', '-0.04214', '0.2515', '0.4238', '-0.1654', '0.10425', '0.4424', '0.28', '0.513', '0.4333', '-0.01536', '0.639', '0.1501', '0.2455', '0.168', '-0.5127', '0.7485', '0.2152', '-0.05365', '-0.1442', '-0.3025', '0.5493', '0.3647', '0.10693', '-0.0993', '-0.4678', '0.3704', '-0.1647', '0.3887', '-0.05185', '0.3838', '-0.2913', '0.03372', '0.394', '0.6772', '0.617', '-0.2003', '0.5825', '0.4043', '-0.4368', '-0.0927', '0.8013', '0.585', '0.1544', '-0.523', '-0.04196', '-0.4016']",,,,,,,
mondo:0014503,autosomal recessive spinocerebellar ataxia 17,"['spinocerebellar ataxia autosomal recessive type 17', 'CWF19L1 autosomal recessive congenital cerebellar ataxia', 'spinocerebellar ataxia, autosomal recessive type 17', 'SCAR17', 'autosomal recessive cerebellar ataxia due to CWF19L1 deficiency', 'spinocerebellar ataxia, autosomal recessive 17', 'autosomal recessive congenital cerebellar ataxia caused by mutation in CWF19L1', 'autosomal recessive spinocerebellar ataxia type 17']",0080064,616127,453521,C4015301,,,,,,,,
mondo:0014504,Perrault syndrome 5,"['PRLTS5', 'TWNK Perrault syndrome', 'Perrault syndrome caused by mutation in TWNK', 'Perrault syndrome type 5', 'Perrault syndrome 5']",,616138,,C4015307,,,,,,,,
mondo:0014505,"developmental and epileptic encephalopathy, 27","['epileptic encephalopathy, early infantile, type 27', 'DEE27', 'GRIN2B early infantile epileptic encephalopathy', 'EIEE27', 'early infantile epileptic encephalopathy caused by mutation in GRIN2B', 'developmental and epileptic encephalopathy 27', 'epileptic encephalopathy, early infantile, 27']",0080444,616139,,C4015316,,,,,,,,
mondo:0014506,hypomyelinating leukodystrophy 9,"['leukodystrophy caused by mutation in RARS', 'leukodystrophy, hypomyelinating, 9', 'RARS-related autosomal recessive hypomyelinating leukodystrophy', 'hypomyelinating leukodystrophy type 9', 'RARS leukodystrophy', 'leukodystrophy, hypomyelinating, type 9', 'HLD9']",0060791,616140,438114,C4015323,"['-0.03177', '0.0543', '0.014786', '-0.0003524', '0.02672', '-0.05414', '-0.002052', '0.05035', '-0.03513', '0.007095', '-0.0245', '-0.0003803', '0.00684', '-0.0238', '0.00745', '-0.02061', '0.01614', '-0.03162', '-0.009674', '-0.0708', '0.001669', '-0.01779', '0.01118', '-0.0007954', '0.02286', '-0.02478', '-0.008446', '0.001055', '-0.002811', '-0.02661', '0.01717', '-0.0057', '0.0545', '0.012314', '0.010735', '-0.02441', '-0.005966', '-0.02307', '0.00908', '-0.0298', '0.01435', '-0.0461', '0.012054', '-0.01437', '-0.0004504', '-0.04462', '0.0008507', '0.02628', '0.002853', '0.012856', '-0.001889', '-0.01102', '-0.018', '-0.01306', '-0.01145', '-0.01921', '0.03714', '-0.02573', '-0.05197', '0.01408', '0.03177', '0.0245', '0.0146', '0.00927', '-0.006435', '0.00577', '0.04718', '0.03986', '-0.0351', '0.04858', '-0.01458', '0.02573', '0.002228', '-0.0337', '0.02707', '0.03084', '0.00736', '0.002468', '-0.03348', '-0.04285', '-0.002766', '-0.00625', '-0.007137', '0.03204', '-0.01341', '0.01308', '0.02', '0.0464', '0.04352', '0.01753', '0.03284', '0.03925', '0.011284', '0.01729', '0.08105', '0.01486', '0.0429', '-0.04196', '0.004467', '0.015']",,,,,,,
mondo:0014507,Catel-Manzke syndrome,"['Catel Manzke syndrome', 'Catel-Manzke syndrome', 'index finger anomaly-Pierre Robin syndrome', 'hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome', 'Pierre Robin sequence-hyperphalangy-clinodactyly syndrome', 'Palatodigital syndrome, Catel-Manzke type', 'index finger anomaly with Pierre Robin syndrome', 'Pierre Robin syndrome-hyperphalangy-clinodactyly syndrome', 'Pierre Robin syndrome with hyperphalangy and clinodactyly', 'CATMANS', 'micrognathia digital syndrome', 'Palatodigital syndrome Catel-Manzke type']",0081122,616145,1388,C1844887,"['0.09344', '-0.4138', '0.2278', '0.1375', '0.3323', '-0.4165', '0.2817', '0.9863', '-0.972', '-1.178', '-0.524', '-0.446', '0.377', '0.3208', '-0.11993', '-0.1334', '-0.014725', '-0.4626', '-0.341', '-0.4897', '0.11444', '0.338', '0.02621', '-0.2637', '0.05746', '0.02484', '-0.5513', '0.163', '1.117', '-0.1034', '-0.1288', '0.3123', '0.2135', '0.1932', '0.2384', '-0.3674', '0.1681', '-0.784', '-0.3855', '-0.5107', '-0.2428', '0.4097', '0.3457', '0.0845', '0.1875', '-0.08014', '-0.05902', '0.6304', '0.02783', '0.1888', '-0.5747', '-0.2356', '0.2046', '-0.1388', '-0.3098', '-0.86', '-0.0972', '0.2179', '-0.1849', '0.3977', '0.2903', '0.3638', '0.2593', '-0.11194', '0.10645', '-0.7397', '0.664', '-0.03696', '-0.1372', '-0.05945', '-0.08124', '0.648', '-0.2766', '-0.1967', '0.2505', '0.1179', '0.4558', '-0.4065', '-0.844', '0.2695', '0.4363', '-0.1237', '0.548', '0.793', '-0.1942', '0.505', '0.1594', '0.1622', '-0.3582', '0.378', '-0.02797', '0.255', '-0.1058', '0.711', '0.4917', '-0.2407', '0.77', '-0.847', '0.03787', '0.182']",,,C535347,,,,
mondo:0014508,vitelliform macular dystrophy 4,"['vitelliform macular dystrophy caused by mutation in IMPG1', 'macular dystrophy, vitelliform, 4', 'IMPG1 vitelliform macular dystrophy', 'VMD4', 'macular dystrophy, vitelliform, type 4']",,616151,,C4015342,,,,,,,,
mondo:0014509,vitelliform macular dystrophy 5,"['macular dystrophy, vitelliform, 5', 'macular dystrophy, vitelliform, type 5', 'VMD5', 'vitelliform macular dystrophy caused by mutation in IMPG2', 'IMPG2 vitelliform macular dystrophy']",,616152,,C4015343,,,,,,,,
mondo:0014510,fatty acyl-CoA reductase 1 deficiency,"['fatty acyl-CoA reductase 1 deficiency', 'severe intellectual disability-epilepsy-cataract syndrome due to FAR1 deficiency', 'fatty acyl-CoA reductase 1 disorder', 'FAR1 deficiency', 'PFCRD', 'fatty acyl-CoA reductase 1 disorder or fatty acyl-CoA reductase 1 deficiency', 'peroxisomal fatty acyl-CoA reductase 1 disorder', 'severe intellectual disability-epilepsy-cataract syndrome due to peroxisomal disorder', 'rhizomelic chondrodysplasia punctata type 4']",0081243,616154,438178,C4015344,,,,,,,,
mondo:0014511,Charcot-Marie-Tooth disease axonal type 2S,"['IGHMBP2 Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2S', 'Charcot-Marie-Tooth neuropathy, type 2S', 'Charcot-Marie-Tooth disease, axonal, type 2S', 'Charcot-Marie-Tooth disease type 2S', 'Charcot-Marie-Tooth neuropathy type 2S', 'autosomal recessive axonal Charcot-Marie-Tooth type 2S', 'CMT2S', 'Charcot-Marie-Tooth disease caused by mutation in IGHMBP2']",0110171,616155,443073,C4015349,,,,,,,,
mondo:0014512,PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome due to a point mutation,"['mental retardation, autosomal dominant type 31', 'MRD31', 'intellectual disability, autosomal dominant type 31', 'neurodevelopmental disorder with neonatal respiratory insufficiency, hypotonia, and feeding difficulties', 'autosomal dominant non-syndromic intellectual disability 31', 'intellectual disability, autosomal dominant 31', 'autosomal dominant mental retardation 31', 'mental retardation, autosomal dominant 31', 'autosomal dominant intellectual disability 31']",0070061,616158,438216,CN237609,"['-0.06757', '0.0991', '0.02069', '0.04242', '0.0481', '-0.1528', '-0.00982', '0.1593', '-0.0945', '-0.0835', '0.002262', '-0.00446', '0.000377', '0.0228', '-0.02553', '-0.04758', '-0.02289', '-0.02455', '-0.05447', '-0.1775', '-0.0005436', '-0.03748', '0.11255', '-0.0313', '0.04538', '-0.01043', '-0.00443', '0.01401', '0.03748', '-0.0356', '0.1067', '0.01548', '0.1267', '0.06775', '-0.00943', '-0.0734', '-0.02403', '-0.063', '-0.007996', '-0.1334', '0.0355', '-0.1229', '0.01715', '-0.05243', '-0.02277', '-0.08545', '-0.03114', '0.03577', '0.05933', '0.071', '-0.0523', '-0.04523', '0.0105', '0.0103', '-0.05', '-0.0484', '0.121', '-0.03568', '-0.0889', '0.03235', '0.0664', '0.04514', '0.001982', '0.01088', '0.0325', '0.04147', '0.12225', '0.0914', '-0.10846', '0.11615', '-0.09454', '0.002537', '0.02928', '-0.0814', '0.04907', '0.0732', '0.0546', '0.02855', '-0.0716', '-0.00802', '-0.02168', '0.01154', '-0.06775', '0.077', '0.012314', '0.005474', '0.04514', '0.1057', '0.1802', '0.02301', '0.06714', '0.08984', '-0.04', '-0.0087', '0.2279', '0.06824', '0.0968', '-0.1771', '0.0186', '0.02124']",,,,,,,
mondo:0014513,nemaline myopathy 10,"['nemaline myopathy caused by mutation in LMOD3', 'nemaline myopathy type 10', 'LMOD3 nemaline myopathy', 'NEM10', 'nemaline myopathy 10']",0110931,616165,,C4015360,,,,,,,,
mondo:0014514,"aortic aneurysm, familial thoracic 9","['aortic aneurysm, familial thoracic 9', 'aortic aneurysm, thoracic, with or without aortic dissection', 'AAT9', 'aortic aneurysm, familial thoracic type 9', 'familial thoracic aortic aneurysm and aortic dissection caused by mutation in MFAP5', 'MFAP5 familial thoracic aortic aneurysm and aortic dissection']",,616166,,C4015368,,,,,,,,
mondo:0014515,macular dystrophy with central cone involvement,"['macular dystrophy with central cone involvement', 'CCMD']",,616170,,C4015371,,,,,,,,
mondo:0014516,microcephaly and chorioretinopathy 2,"['MCCRP2', 'microcephaly and chorioretinopathy caused by mutation in PLK4', 'microcephaly and chorioretinopathy, autosomal recessive, type 2', 'microcephaly and chorioretinopathy, autosomal recessive, 2', 'PLK4 microcephaly and chorioretinopathy', 'microcephaly and chorioretinopathy type 2']",0080106,616171,,C4015388,,,,,,,,
mondo:0014517,"generalized epilepsy with febrile seizures plus, type 9","['generalised epilepsy with febrile seizures plus caused by mutation in STX1B', 'STX1B generalised epilepsy with febrile seizures plus', 'generalised epilepsy with febrile seizures plus caused by mutation in STX1b', 'generalized epilepsy with febrile seizures plus, type 9', 'generalized epilepsy with febrile seizures plus caused by mutation in STX1b', 'STX1b generalised epilepsy with febrile seizures plus', 'GEFSP9', 'STX1b generalized epilepsy with febrile seizures plus', 'Gefs+, type 9', 'STX1B generalized epilepsy with febrile seizures plus']",0111301,616172,,C4015395,,,,,,,,
mondo:0014518,platelet-type bleeding disorder 19,"['PRKACG isolated hereditary giant platelet disorder', 'BDPLT19', 'isolated hereditary giant platelet disorder caused by mutation in PRKACG', 'severe autosomal recessive macrothrombocytopenia', 'bleeding disorder, platelet-type, 19']",0111048,616176,438207,C4015405,"['-0.04', '0.03586', '-0.01234', '-0.02037', '0.01165', '-0.06122', '-0.001596', '0.05823', '-0.0359', '-0.012764', '-0.01793', '0.01316', '-0.001125', '-0.006184', '-0.00974', '-0.02861', '0.003214', '-0.01388', '-0.01491', '-0.08997', '-0.01518', '0.001773', '0.0498', '-0.02986', '0.02074', '-0.02664', '0.001611', '-0.005814', '-0.00467', '-0.0447', '0.01125', '-0.01145', '0.0449', '0.02577', '0.02443', '-0.011215', '-0.0218', '-0.01933', '0.01335', '-0.05936', '0.02498', '-0.0447', '0.0104', '-0.03766', '0.002945', '-0.0521', '-0.02441', '0.03482', '0.00617', '0.02892', '0.01029', '-0.01825', '0.007187', '0.006737', '-0.02779', '-0.002146', '0.05133', '-0.01321', '-0.0514', '-0.002224', '0.02235', '0.0383', '0.01843', '-0.00903', '-0.003006', '0.01749', '0.05032', '0.02954', '-0.0536', '0.04846', '-0.02567', '-0.00345', '0.00409', '-0.04294', '0.03574', '0.02092', '0.03473', '-0.002335', '-0.02272', '-0.0201', '-0.0182', '-0.00864', '-0.004047', '0.04572', '-0.0002372', '0.02292', '0.01935', '0.07056', '0.06775', '-0.01624', '0.02657', '0.05862', '-0.00989', '0.01173', '0.10516', '0.04266', '0.04544', '-0.0665', '-0.006332', '0.02376']",,,,,,,
mondo:0014519,"chronic mountain sickness, susceptibility to","['chronic mountain sickness, susceptibility to', 'Monge disease']",,616182,,C0274294,,,,,,,,
mondo:0014520,"46,XX ovarian dysgenesis-short stature syndrome","['ovarian dysgenesis 4', 'ODG4', 'ovarian dysgenesis type 4']",0080496,616185,444048,C4015409,,,,,,,,
mondo:0014521,progressive myoclonic epilepsy type 7,"['meak', 'EPM7', 'PME type 7', 'epilepsy, progressive myoclonic 7', 'progressive myoclonus epilepsy type 7', 'KCNC1 progressive myoclonic epilepsy', 'progressive myoclonic epilepsy due to KV3.1 deficiency', 'myoclonus epilepsy and ataxia due to potassium channel mutation', 'epilepsy, progressive myoclonic type 7', 'progressive myoclonic epilepsy caused by mutation in KCNC1']",0111447,616187,435438,C4015420,,C142804,,,,,,
mondo:0014522,retinal dystrophy and obesity,"['RDOB', 'retinal dystrophy and obesity']",,616188,,C4015424,,,,,,,,
mondo:0014523,juvenile-onset diabetes mellitus-central and peripheral neurodegeneration syndrome,"['ACPHD', 'combined cerebellar and peripheral ataxia-hearing loss-diabetes mellitus syndrome', 'ataxia, combined cerebellar and peripheral, with hearing loss and diabetes mellitus']",,616192,445062,C4015436,,,,,,,,
mondo:0014524,"intellectual disability, autosomal recessive 47","['FMN2 autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive type 47', 'MRT47', 'intellectual developmental disorder, autosomal recessive 47', 'autosomal recessive non-syndromic intellectual disability caused by mutation in FMN2', 'intellectual disability, autosomal recessive 47', 'mental retardation, autosomal recessive 47', 'intellectual disability, autosomal recessive type 47']",0081211,616193,,C4015444,,,,,,,,
mondo:0014525,combined oxidative phosphorylation defect type 23,"['GTPBP3 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 23', 'COXPD23', 'combined oxidative phosphorylation deficiency type 23', 'combined oxidative phosphorylation deficiency caused by mutation in GTPBP3']",0111500,616198,444013,C4015447,"['-0.4666', '0.3015', '0.0545', '-0.1296', '-0.04205', '-0.2372', '0.1581', '0.4304', '-0.3896', '0.1406', '-0.4055', '-0.4268', '0.09174', '-0.329', '0.2343', '-0.2285', '-0.0759', '-0.4875', '-0.458', '-0.6426', '0.2107', '-0.2284', '0.3857', '0.2356', '0.2515', '-0.1648', '0.2542', '0.2615', '-0.282', '-0.06396', '0.119', '0.2172', '0.7236', '0.1985', '0.02927', '-0.1763', '-0.05484', '-0.175', '0.1346', '-0.0661', '0.11646', '-0.2239', '0.1066', '0.489', '-0.3562', '-0.2482', '0.0971', '0.03134', '-0.2095', '-0.2294', '0.069', '-0.04105', '-0.04437', '-0.0504', '-0.2043', '-0.09235', '0.278', '0.1943', '-0.1177', '0.315', '-0.05246', '0.00152', '0.5063', '0.0325', '-0.572', '0.267', '0.378', '0.4224', '-0.4375', '0.2883', '-0.2196', '0.2274', '-0.02676', '0.04266', '0.1461', '-0.0734', '0.2388', '-0.2152', '-0.1287', '0.1969', '0.08655', '-0.0474', '0.08966', '0.257', '0.12274', '-0.227', '0.283', '0.5317', '0.573', '0.1326', '0.528', '0.2194', '0.04428', '-0.08405', '0.6064', '0.513', '0.3264', '-0.1001', '0.2268', '-0.03738']",,0009033,,,,,
mondo:0014526,polyglucosan body myopathy type 2,"['GYG1 polyglucosan body myopathy', 'polyglucosan body myopathy caused by mutation in GYG1', 'polyglucosan body myopathy type 2', 'polyglucosan body myopathy 2', 'PGBM2']",,616199,456369,C4015452,,,,,,,,
mondo:0014527,progeroid features-hepatocellular carcinoma predisposition syndrome,"['RUIJS-Aalfs syndrome', 'RJALS', 'Ruijs-Aalfs syndrome']",0111264,616200,435953,C4015461,"['0.00249', '0.01219', '0.00971', '-9.39e-05', '0.002483', '-0.01546', '-0.003405', '0.01857', '-0.01001', '-0.01475', '-0.00393', '-0.002638', '0.00442', '0.0006127', '-0.00432', '-0.008896', '-0.004086', '0.0005064', '-0.010574', '-0.02136', '0.00535', '0.000659', '0.01639', '-0.01205', '0.005142', '-0.004223', '-0.00578', '0.003513', '-0.001071', '-0.003637', '0.012985', '-0.002407', '0.02171', '0.01098', '0.011', '-0.002424', '-0.0010805', '-0.007534', '-0.00406', '-0.013145', '-0.004314', '-0.01843', '0.01308', '-0.00515', '0.001759', '-0.01258', '-0.003593', '0.003841', '0.00397', '0.005775', '-0.012314', '-0.008484', '-0.001854', '0.003294', '-0.00543', '-0.01148', '0.002838', '-0.01079', '-0.02716', '-0.003004', '0.01041', '0.004486', '-0.00573', '-0.006443', '0.00357', '-0.0003765', '0.01979', '0.02333', '-0.00654', '0.01666', '-0.01894', '0.002113', '0.01061', '-0.00337', '0.0002314', '0.00931', '0.00541', '-0.002958', '-0.01625', '-0.01958', '0.001206', '0.00672', '-0.001987', '0.002789', '-2.14e-05', '-0.00823', '0.00685', '0.00942', '0.02037', '-0.001439', '0.00772', '0.01646', '0.006924', '0.00762', '0.03442', '0.0161', '0.0189', '-0.01698', '-0.01049', '0.0024']",,,,,,,
mondo:0014528,chronic atrial and intestinal dysrhythmia,"['Cohesinopathy affecting heart and gut rhythm', 'caid', 'chronic atrial and intestinal dysrhythmia', 'caid syndrome', 'chronic atrial intestinal dysrhythmia syndrome', 'chronic atrial and intestinal dysrhythmia syndrome', 'chronic atrial dysrhythmia-intestinal motility disorder']",0060339,616201,435988,C4015474,"['-0.0154', '0.03317', '0.01342', '-0.01918', '0.01697', '-0.02583', '0.00889', '0.06152', '-0.01566', '-0.0266', '-0.012695', '-0.01552', '-0.006157', '0.02388', '-0.04587', '-0.03613', '0.0003498', '-0.01231', '-0.03625', '-0.1026', '0.005035', '-0.01892', '0.03625', '-0.03558', '0.0319', '-0.03983', '0.0077', '0.010376', '0.02843', '-0.01095', '0.0381', '-0.0121', '0.06195', '0.0184', '0.02211', '-0.02875', '-0.01276', '-0.00753', '-0.01694', '-0.04193', '-0.000989', '-0.03494', '0.0393', '-0.01978', '-0.002071', '-0.05185', '-0.02359', '0.05557', '0.01616', '0.02458', '-0.02199', '0.01264', '0.02122', '0.01041', '-0.0372', '-0.01657', '0.0383', '-0.03452', '-0.06915', '-0.004772', '0.05154', '0.02475', '0.01764', '-0.00564', '0.01261', '-0.0002973', '0.07684', '0.0736', '-0.0638', '0.0621', '-0.0332', '-0.00857', '0.004997', '-0.02707', '-0.00487', '0.02663', '0.01733', '-0.00803', '-0.0295', '-0.03726', '-0.01674', '-0.01845', '-0.01539', '0.02673', '-0.01892', '0.005367', '0.02988', '0.01811', '0.04645', '-0.01837', '0.01448', '0.02513', '0.002886', '0.00854', '0.0991', '0.04437', '0.0596', '-0.06125', '-0.01955', '0.0393']",,,,,,,
mondo:0014529,cerebellar-facial-dental syndrome,"['Cerebellofaciodental syndrome', 'cerebellar-facial-dental syndrome', 'CEREBELLOFACIODENTAL syndrome', 'CFDS']",0080898,616202,444072,CN221667,"['-0.10706', '-0.03308', '0.2467', '-0.2305', '0.3645', '-0.10034', '0.186', '1.21', '-0.5146', '-0.7407', '-0.3694', '-0.2568', '0.1519', '-0.1464', '0.3323', '-0.2917', '-0.03775', '-0.3018', '-0.453', '-0.4185', '0.4954', '0.1346', '0.03607', '-0.315', '0.4285', '-0.1439', '-0.3862', '0.1769', '0.2362', '0.1869', '0.2455', '0.2034', '0.665', '-0.10266', '0.0336', '0.06506', '-0.0625', '-0.3057', '-0.1421', '-0.127', '0.05368', '0.03897', '0.3616', '-0.1186', '0.0566', '-0.3867', '-0.1047', '0.1171', '-0.612', '-0.436', '0.1032', '0.0914', '-0.5234', '-0.02124', '-0.5576', '-0.262', '-0.0849', '0.0655', '-0.1743', '0.095', '0.2026', '0.0892', '-0.2751', '0.2273', '-0.358', '-0.3203', '0.1991', '0.2507', '-0.1503', '0.008995', '-0.296', '0.6353', '-0.02136', '-0.4478', '0.04712', '-0.05545', '0.3652', '-0.1897', '-0.591', '-0.2161', '0.1326', '0.006798', '-0.306', '0.5464', '-0.1093', '0.2004', '0.2256', '0.646', '-0.0849', '0.2063', '0.3962', '0.376', '-0.5376', '0.1216', '0.5967', '-0.02461', '0.5396', '-0.3896', '0.834', '0.3066']",,0009030,,,,,
mondo:0014530,autosomal recessive spinocerebellar ataxia 18,"['SCAR18', 'GRID2 autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome', 'GRID2 autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome', 'autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency', 'spinocerebellar ataxia, autosomal recessive 18', 'autosomal recessive congenital cerebellar ataxia due to ionotropic glutamate receptor delta-2 subunit deficiency', 'autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome caused by mutation in GRID2', 'spinocerebellar ataxia, autosomal recessive type 18', 'autosomal recessive spinocerebellar ataxia type 18']",0080042,616204,363432,C4015505,"['-0.253', '-0.2037', '0.06134', '0.005894', '-0.2141', '-1.076', '0.2708', '0.1412', '-0.73', '-0.664', '0.2153', '0.202', '-0.11194', '-0.003204', '0.544', '-0.3914', '-0.0841', '-0.2898', '-0.1207', '-1.023', '-0.146', '-0.2893', '0.1777', '-0.3904', '0.483', '-0.3484', '-0.371', '0.1808', '-0.1346', '-0.7793', '0.01912', '0.4375', '-0.3726', '-0.1866', '0.2908', '0.11273', '-0.2148', '0.000978', '0.51', '0.299', '0.4429', '0.1882', '-0.4226', '0.5596', '0.3586', '-0.5845', '0.1843', '0.5425', '0.33', '-0.02167', '-0.318', '0.3723', '-0.08826', '-0.6143', '0.02051', '-0.9395', '0.4163', '0.5415', '-0.1896', '0.599', '-0.541', '0.1472', '0.386', '-0.232', '-0.5083', '0.4724', '0.1796', '0.585', '-0.4253', '0.3662', '0.8184', '0.6235', '-0.2075', '-0.5605', '0.769', '0.2269', '0.3633', '0.4204', '0.1781', '0.4', '-0.4907', '-0.803', '0.3354', '1.046', '-0.2493', '-0.532', '0.1891', '0.1003', '0.573', '0.65', '0.6167', '0.6113', '0.0004876', '0.0607', '0.856', '1.173', '0.4675', '0.4897', '-0.243', '-0.04465']",,,,,,,
mondo:0014531,amyotrophic lateral sclerosis type 22,"['amyotrophic lateral sclerosis caused by mutation in TUBA4A', 'ALS 22', 'ALS22', 'amyotrophic lateral sclerosis 22 with or without frontotemporal dementia', 'amyotrophic lateral sclerosis type 22', 'amyotrophic lateral sclerosis 22', 'TUBA4A amyotrophic lateral sclerosis']",0060355,616208,,C4015512,,,,,,,,
mondo:0014532,autosomal dominant mitochondrial myopathy with exercise intolerance,"['myopathy, isolated mitochondrial, autosomal dominant', 'IMMD']",0081357,616209,457050,C4015513,,,,,,,,
mondo:0014533,"developmental and epileptic encephalopathy, 28","['early infantile epileptic encephalopathy caused by mutation in WWOX', 'WWOX early infantile epileptic encephalopathy', 'EIEE28', 'developmental and epileptic encephalopathy 28', 'WWOX-related epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 28', 'epileptic encephalopathy, early infantile, type 28', 'WOREE syndrome', 'DEE28']",0080452,616211,,C4015519,,,,,,,,
mondo:0014534,lissencephaly 6 with microcephaly,"['KATNB1 Microlissencephaly', 'lissencephaly 6 with microcephaly', 'KATNB1 microlissencephaly', 'Microlissencephaly caused by mutation in KATNB1', 'lissencephaly 6, with microcephaly', 'LIS6']",0112236,616212,,,,,,,,,,
mondo:0014535,hyperproinsulinemia,['hyperproinsulinemia'],,616214,,C0342283,,,,C562776,250.80,,,
mondo:0014536,thrombocytopenia 5,"['ETV6 thrombocytopenia', 'THC5', 'thrombocytopenia caused by mutation in ETV6', 'thrombocytopenia type 5', 'thrombocytopenia, autosomal dominant, 5', 'thrombocytopenia 5', 'thrombocytopenia 5 with increased susceptibility to malignancy']",,616216,,C4015537,,,,,,,,
mondo:0014537,nephronophthisis 19,"['nephronophthisis type 19', 'nephronophthisis 19', 'DCDC2 nephronophthisis (disease)', 'NPHP19']",0111126,616217,,C4015542,,,,,,,,
mondo:0014538,"fibrosis of extraocular muscles, congenital, 5","['fibrosis of extraocular muscles, congenital, 5', 'congenital fibrosis of extraocular muscles caused by mutation in COL25A1', 'COL25A1 congenital fibrosis of extraocular muscles', 'fibrosis of extraocular muscles, congenital, type 5', 'CFEOM5']",0081020,616219,,C4015552,,,,,,,,
mondo:0014539,focal segmental glomerulosclerosis 9,"['focal segmental glomerulosclerosis type 9', 'glomerulosclerosis, focal segmental, 9', 'CRB2 focal segmental glomerulosclerosis', 'focal segmental glomerulosclerosis caused by mutation in CRB2', 'FSGS9', 'focal segmental glomerulosclerosis 9']",0111134,616220,,C4015555,,,,,,,,
mondo:0014540,amelogenesis imperfecta type 1H,"['AI1H', 'ITGB6 amelogenesis imperfecta', 'amelogenesis imperfecta, type 1H', 'amelogenesis imperfecta caused by mutation in ITGB6', 'amelogenesis imperfecta, type IH', 'amelogenesis imperfecta type IH']",0110064,616221,,C4015557,,,,,,,,
mondo:0014541,motor developmental delay due to 14q32.2 paternally expressed gene defect,"['maternal uniparental disomy chromosome 14 syndrome', 'uniparental disomy, maternal, chromosome 14', 'mUPD14 syndrome', 'TEMPLE syndrome']",0111713,616222,254516,C4015558,,C120409,,,,,,
mondo:0014542,congenital myasthenic syndrome 15,"['myasthenic syndrome, congenital, type 15', 'myasthenic syndrome, congenital, 15, without tubular aggregates', 'congenital myasthenic syndrome type 15', 'ALG14 congenital myasthenic syndrome', 'myasthenic syndrome, congenital, 15', 'congenital myasthenic syndrome 15 without tubular aggregates', 'myasthenic syndrome, congenital, without tubular aggregates', 'CMS15', 'congenital myasthenic syndrome caused by mutation in ALG14']",0110658,616227,,C4015596,,,,,,,,
mondo:0014543,congenital myasthenic syndrome 14,"['ALG2 congenital myasthenic syndromes with glycosylation defect', 'congenital myasthenic syndrome 14, with tubular aggregates', 'myasthenic syndrome, congenital, type 14', 'congenital myasthenic syndromes with glycosylation defect caused by mutation in ALG2', 'myasthenic syndrome, congenital, 14, with tubular aggregates', 'CMSTA3', 'myasthenic syndrome, congenital, 14', 'myasthenic syndrome, congenital, with tubular aggregates 3', 'CMS14', 'congenital myasthenic syndrome type 14', 'congenital myasthenic syndrome with tubular aggregates 3']",0110669,616228,,C4015597,,,,,,,,
mondo:0014544,osteogenesis imperfecta type 16,"['chromosome 11P11.2 deletion syndrome, 91.3-Kb', 'OI, type 16', 'osteogenesis imperfecta, type XVI', 'OI16', 'osteogenesis imperfecta, type 16', 'chromosome 11p11.2 deletion syndrome 91.3-KB', 'osteogenesis imperfecta type XVI']",0110345,616229,216812,C4015610,,,,,,,,
mondo:0014545,progressive myoclonic epilepsy type 8,"['CERS1 progressive myoclonic epilepsy', 'progressive myoclonic epilepsy caused by mutation in CERS1', 'EPM8', 'progressive myoclonus epilepsy type 8', 'epilepsy, progressive myoclonic, type 8', 'epilepsy, progressive myoclonic, 8', 'progressive myoclonic epilepsy due to CERS1 deficiency', 'PME type 8']",0111451,616230,424027,C4015619,,,,,,,,
mondo:0014546,myopathy due to calsequestrin and SERCA1 protein overload,"['VMCQA', 'myopathy, vacuolar, with CASQ1 aggregates']",,616231,88635,C4510368,"['-0.517', '0.0662', '-0.05942', '-0.2944', '0.1103', '-0.1521', '-0.1656', '0.435', '-0.2644', '-0.02869', '-0.1714', '0.02417', '0.1934', '0.04868', '-0.1375', '-0.066', '-0.23', '0.1462', '-0.3943', '-0.633', '0.1653', '-0.1182', '0.259', '0.3928', '0.05804', '0.01837', '0.1203', '-0.2517', '-0.02727', '-0.10065', '0.2339', '0.1494', '0.3975', '0.08514', '-0.2793', '-0.451', '-0.2018', '-0.1887', '0.11456', '-0.474', '-0.1716', '-0.2051', '0.1421', '0.1466', '-0.2344', '-0.102', '0.00816', '0.1409', '0.05484', '-0.138', '-0.1178', '-0.0267', '0.4087', '-0.11945', '-0.0395', '-0.07684', '0.264', '-0.4497', '-0.2107', '0.1788', '0.289', '0.1864', '0.2942', '-0.4224', '-0.2432', '0.011314', '0.2708', '0.4004', '-0.5786', '0.05807', '-0.2651', '0.0607', '-0.0301', '0.06445', '0.2812', '0.007343', '0.2201', '0.10004', '0.118', '0.06158', '0.0626', '-0.02087', '-0.0884', '-0.0466', '-0.01558', '0.12054', '-0.04037', '0.4531', '0.4114', '-0.08154', '0.4133', '0.2654', '-0.1621', '-0.2444', '0.4358', '0.528', '0.1289', '-0.4067', '-0.266', '0.1313']",,,,,,,
mondo:0014547,combined oxidative phosphorylation defect type 24,"['combined oxidative phosphorylation deficiency type 24', 'NARS2 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 24', 'COXPD24', 'combined oxidative phosphorylation deficiency caused by mutation in NARS2']",0111485,616239,444458,C4015643,"['-0.569', '0.1351', '0.02884', '-0.05515', '-0.05252', '-0.614', '0.1418', '0.425', '-0.374', '0.05624', '-0.2462', '-0.3447', '0.0662', '-0.2986', '0.104', '-0.1917', '0.2091', '-0.1531', '-0.268', '-0.708', '0.2386', '-0.2382', '0.2646', '0.0967', '0.172', '-0.1142', '0.002754', '0.1586', '-0.2776', '-0.06354', '0.082', '0.381', '0.5728', '0.3428', '-0.02289', '-0.2576', '-0.0676', '-0.2302', '-0.1087', '0.012695', '0.2235', '-0.3313', '-0.0798', '0.3306', '-0.307', '-0.3247', '0.0162', '-0.01984', '-0.0876', '0.00847', '-0.125', '-0.1293', '0.1393', '-0.3137', '-0.02612', '-0.1792', '0.2145', '0.04688', '0.01753', '0.2964', '-0.1003', '-0.0556', '0.613', '-0.01324', '-0.2112', '0.1497', '0.16', '0.2932', '-0.4292', '0.2', '-0.02254', '0.243', '-0.1193', '-0.2563', '0.1121', '0.0746', '0.2637', '-0.11774', '-0.1549', '0.3354', '0.1953', '0.00962', '-0.1097', '0.409', '0.0872', '-0.2817', '0.1259', '0.4927', '0.2095', '0.375', '0.6895', '0.1738', '0.09155', '-0.0975', '0.641', '0.479', '0.378', '-0.3706', '0.355', '0.1666']",,0009034,,,,,
mondo:0014548,long QT syndrome 14,"['long QT syndrome 14', 'LQT14', 'long QT syndrome type 14', 'CALM1 long QT syndrome', 'long QT syndrome caused by mutation in CALM1']",0110655,616247,101016,C4015671,"['-0.0335', '0.07715', '0.0347', '-0.007633', '0.03069', '-0.1449', '0.05276', '0.1367', '-0.05856', '-0.0796', '0.02193', '0.03093', '0.0825', '0.005436', '-0.0726', '-0.07886', '0.03029', '-0.04263', '0.03', '-0.1581', '0.06064', '-0.006176', '0.05685', '-0.0419', '0.0407', '-0.07104', '0.02153', '0.0006194', '0.02263', '-0.0547', '0.1239', '-0.00895', '0.11365', '0.04245', '0.008484', '-0.1032', '-0.014206', '-0.0718', '-0.01542', '-0.0947', '0.0701', '-0.1148', '0.0713', '-0.06964', '0.008125', '-0.0731', '-0.0724', '0.1378', '0.01015', '0.0307', '-0.067', '-0.05524', '-0.0613', '0.0384', '-0.046', '-0.07007', '0.07965', '-0.03128', '-0.06635', '0.035', '0.1059', '0.02557', '-0.03598', '0.004143', '-0.0438', '0.01075', '0.0754', '0.0356', '-0.12024', '0.1381', '-0.1022', '0.01409', '0.04337', '-0.1135', '-0.01514', '0.07855', '0.02403', '-0.02579', '-0.0882', '-0.0399', '0.01295', '0.0413', '-0.03223', '0.05783', '-0.01308', '0.0491', '-0.02487', '0.1299', '0.08466', '0.014244', '-0.0151', '0.0821', '0.0359', '0.05502', '0.2229', '0.05496', '0.1147', '-0.2124', '-0.00969', '0.02328']",C177534,,,,,,
mondo:0014549,lethal congenital contracture syndrome 6,"['lethal congenital contracture syndrome type 6', 'lethal congenital contracture syndrome 6', 'ZBTB42 lethal congenital contracture syndrome', 'LCCS6', 'lethal congenital contracture syndrome caused by mutation in ZBTB42']",,616248,,C4015686,,,,,,,,
mondo:0014550,long QT syndrome 15,"['LQT15', 'long QT syndrome caused by mutation in CALM2', 'long QT syndrome 15', 'CALM2 long QT syndrome', 'long QT syndrome type 15']",0110656,616249,101016,C4015695,,,,,,,,
mondo:0014551,short stature with nonspecific skeletal abnormalities,"['short stature with nonspecific skeletal abnormalities', 'SNSK']",,616255,,C4225399,,,,,,,,
mondo:0014552,lethal fetal cerebrorenogenitourinary agenesis/hypoplasia syndrome,"['MKS12', 'Meckel syndrome type 12', 'Meckel syndrome 12']",,616258,439897,C4015701,,,,,,,,
mondo:0014553,Tenorio syndrome,"['TNORS', 'Tenorio syndrome', 'TENORIO syndrome', 'overgrowth, macrocephaly, and intellectual disability syndrome']",,616260,,C4015710,"['0.007504', '-0.00564', '0.00815', '0.00779', '0.002974', '-0.00769', '-0.00888', '0.00453', '-0.0002599', '-0.00962', '-0.009445', '0.00571', '0.00114', '0.00938', '-0.00055', '0.00738', '-0.003408', '0.000254', '-0.01177', '-0.000539', '-0.002222', '-0.00851', '-0.0002806', '0.002314', '-0.00471', '0.001805', '-0.010635', '-0.001816', '0.00283', '-0.00607', '0.010864', '-0.007084', '0.002832', '0.010735', '0.0004997', '0.00886', '0.005188', '-0.00826', '-0.00637', '-0.0116', '-0.001869', '-0.0094', '-0.006035', '-0.00508', '-0.002697', '0.002594', '-0.00475', '0.003176', '0.002441', '-0.003284', '0.003357', '-0.00915', '0.003218', '0.002031', '0.004654', '-3.01e-05', '-0.003563', '-0.0009246', '0.003994', '0.003544', '-0.005943', '0.002628', '0.006905', '-0.00558', '-0.00879', '0.0054', '-0.001778', '-0.004635', '0.005714', '0.002995', '-0.00909', '-0.004883', '0.008575', '0.001735', '-0.00331', '-0.007656', '-0.0004435', '0.00217', '0.006725', '0.00156', '-0.0005736', '0.0013275', '0.00837', '-0.00459', '-0.001952', '6.04e-05', '0.00538', '-0.001199', '-0.004166', '0.002373', '0.003551', '-0.001151', '-0.004375', '-0.00932', '0.00933', '0.00742', '0.0008087', '-0.015495', '0.007324', '-0.00108']",,,,,,,
mondo:0014555,peeling skin syndrome type A,"['PSS type A', 'non-inflammatory peeling skin syndrome type A', 'non-inflammatory generalised peeling skin syndrome type A.', 'generalised deciduous skin type A', 'non-inflammatory generalized peeling skin syndrome type A.', 'generalised peeling skin syndrome type A', 'peeling skin syndrome 3', 'generalized deciduous skin type A', 'peeling skin syndrome type 3', 'PSS3', 'generalized peeling skin syndrome type A']",,616265,263548,C4015729,"['0.5703', '-0.09784', '-0.477', '-0.3271', '-0.05362', '-0.505', '-0.143', '0.0645', '-0.2925', '-0.1849', '-0.3467', '0.05695', '-0.5454', '-0.337', '-0.1796', '0.4783', '0.551', '-0.2852', '-0.01538', '-0.455', '-0.4285', '-0.1594', '0.533', '-0.6416', '-0.2042', '0.1482', '-0.4705', '0.0895', '-0.3237', '0.0468', '0.1825', '0.0718', '-0.01654', '0.1277', '0.3496', '0.1372', '-0.5894', '-0.5527', '0.1417', '0.0455', '0.2644', '-0.719', '-0.204', '-0.1857', '-0.0698', '0.2344', '-0.5137', '0.3794', '0.4062', '-0.0628', '-0.1167', '-0.2139', '0.6353', '0.0731', '-0.583', '-0.08716', '0.0388', '-0.14', '-0.6245', '-0.578', '-0.1445', '0.11646', '-0.04407', '-0.2319', '0.05988', '0.432', '0.4907', '0.3652', '-0.2727', '0.9546', '-0.232', '-0.502', '-0.323', '-0.0525', '0.062', '0.1602', '-0.2563', '-0.2386', '-0.09924', '-0.2051', '0.05093', '-0.2732', '-0.3115', '0.0316', '-0.05643', '-0.1759', '-0.1461', '0.4944', '0.2544', '0.1434', '0.5874', '0.0818', '0.1555', '0.8384', '0.589', '0.1179', '0.2065', '-0.432', '-0.1066', '-0.2496']",,,,,,,
mondo:0014556,"congenital contractures of the limbs and face, hypotonia, and developmental delay","['CLIFAHDD', 'congenital limbs-face contractures-hypotonia-developmental delay syndrome', 'congenital contractures of the limbs and face, hypotonia, and developmental delay', 'CLIFAHDD syndrome']",0081048,616266,562528,C4225398,"['-0.1243', '0.1187', '0.06012', '-0.1185', '0.08997', '-0.2004', '0.10095', '0.279', '-0.3079', '-0.1064', '-0.1118', '0.002522', '0.07184', '0.0436', '-0.0878', '0.02628', '0.008995', '-0.1124', '-0.11743', '-0.2754', '-0.04297', '-0.03099', '0.1208', '-0.03873', '0.0453', '-0.06134', '-0.0532', '0.008385', '0.02785', '-0.0897', '0.0816', '-0.07043', '0.2335', '0.06226', '0.01256', '-0.01327', '-0.028', '-0.04178', '-0.04977', '-0.1263', '0.02415', '-0.1853', '-0.056', '0.0448', '-0.01529', '-0.06744', '-0.04538', '0.2059', '0.04282', '0.04837', '-0.238', '-0.007324', '0.07086', '-0.00254', '-0.0742', '-0.07074', '0.03693', '-0.05127', '-0.1182', '-0.00427', '-0.00481', '-0.00939', '-0.06573', '0.02011', '-0.0742', '-0.02164', '0.09045', '0.2015', '-0.1598', '0.1613', '-0.1143', '0.1172', '0.103', '-0.0847', '0.01181', '0.0794', '0.0376', '-0.0745', '-0.10315', '-0.0983', '-0.01942', '-0.011925', '0.02333', '0.11273', '-0.0004337', '0.08905', '-0.002474', '0.1407', '0.2255', '0.07623', '0.09656', '0.214', '0.01155', '0.085', '0.178', '0.0944', '0.197', '-0.192', '0.1124', '0.1098']",,1001868,,,,,
mondo:0014557,ataxia - oculomotor apraxia type 4,"['ataxia - oculomotor apraxia type 4', 'oculomotor apraxia or related oculomotor disease caused by mutation in PNKP', 'AOA4', 'ataxia-oculomotor apraxia-4', 'PNKP oculomotor apraxia or related oculomotor disease', 'ataxia-oculomotor apraxia 4']",,616267,459033,C4225397,"['-0.1824', '-0.2352', '-0.04187', '0.1301', '-0.1985', '-0.977', '0.2969', '0.08496', '-0.6006', '-0.9307', '0.2424', '0.2119', '-0.2615', '0.1829', '0.3647', '-0.3757', '-0.1242', '-0.3782', '0.1222', '-0.9976', '-0.129', '-0.3599', '0.188', '-0.555', '0.502', '-0.503', '-0.2046', '0.2078', '-0.10693', '-0.694', '-0.0196', '0.4773', '-0.4434', '-0.1935', '0.3923', '0.0596', '-0.233', '0.1793', '0.4124', '0.4163', '0.2964', '0.136', '-0.4207', '0.55', '0.518', '-0.572', '0.2128', '0.4272', '0.3193', '-0.0774', '-0.1829', '0.1716', '-0.1425', '-0.352', '0.05035', '-0.7554', '0.379', '0.4512', '-0.01341', '0.522', '-0.6484', '0.1593', '0.2399', '-0.1498', '-0.4521', '0.632', '0.2637', '0.5186', '-0.474', '0.5083', '0.9253', '0.56', '-0.0871', '-0.7876', '0.8604', '0.3923', '0.1682', '0.3867', '0.1395', '0.348', '-0.3452', '-0.766', '0.379', '0.7036', '-0.2793', '-0.6743', '0.2527', '-0.1221', '0.5547', '0.578', '0.3354', '0.4116', '0.10956', '0.09186', '0.966', '0.98', '0.3057', '0.1929', '-0.4685', '-0.00984']",,0009016,,,,,
mondo:0014558,autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome,"['autosomal dominant non-syndromic intellectual disability 32', 'KAT6A Syndrome', 'intellectual disability, autosomal dominant 32', 'intellectual disability, autosomal dominant type 32', 'mental retardation, autosomal dominant type 32', 'autosomal dominant intellectual disability 32', 'autosomal dominant mental retardation 32', 'Arboleda-Tham syndrome', 'mental retardation, autosomal dominant 32', 'MRD32']",0070062,616268,457193,,,,,,,,,
mondo:0014559,progressive essential tremor-speech impairment-facial dysmorphism-intellectual disability-abnormal behavior syndrome,"['intellectual disability, autosomal recessive 48', 'MRT48', 'intellectual disability, autosomal recessive type 48', 'mental retardation, autosomal recessive type 48', 'mental retardation, autosomal recessive 48']",0081212,616269,457212,C4225395,,,,,,,,
mondo:0014560,amelogenesis imperfecta type 1F,"['amelogenesis imperfecta, type 1F', 'amelogenesis imperfecta, hypoplastic type 1F', 'amelogenesis imperfecta caused by mutation in AMBN', 'amelogenesis imperfecta hypoplastic type IF', 'amelogenesis imperfecta, type IF', 'amelogenesis imperfecta type IF', 'AI1F', 'AMBN amelogenesis imperfecta']",0110065,616270,,C4225394,,,,,,,,
mondo:0014561,"3-methylglutaconic aciduria, type VIIB","['3-methylglutaconic aciduria with cataracts, neurologic involvement and neutropenia', '3-methylglutaconic aciduria-cataract-neurologic involvement-neutropenia syndrome', 'MEGCANN', '3-Methylglutaconic aciduria, type 7', 'MGCA7', '3-METHYLGLUTACONIC aciduria with cataracts, neurologic involvement, and neutropenia', 'CLPB 3-methylglutaconic aciduria', '3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropenia', 'MGA7', '3-methylglutaconic aciduria type VII', '3-methylglutaconic aciduria type 7']",0110003,616271,445038,C4225393,,,0009014,,,,,
mondo:0014562,neonatal encephalomyopathy-cardiomyopathy-respiratory distress syndrome,"['COQ10D7', 'primary coenzyme Q10 deficiency 7', 'coenzyme Q10 deficiency, primary, 7', 'coenzyme Q10 deficiency, primary, type 7', 'COQ4-related neonatal encephalomyopathy']",0070244,616276,457185,C4225392,,,,,,,,
mondo:0014563,mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency,"['ECHS1D', 'mitochondrial short-chain Enoyl-Coa hydratase 1 deficiency', 'mitochondrial short-chain ENOYL-CoA hydratase 1 deficiency', 'short-chain enoyl-CoA hydratase deficiency']",,616277,,C4225391,,,,,,,,
mondo:0014564,congenital bile acid synthesis defect 5,"['ABCD3 congenital bile acid synthesis defect', 'bile acid synthesis defect, congenital, 5', 'bile acid synthesis defect, congenital, type 5', 'CBAS5', 'congenital bile acid synthesis defect caused by mutation in ABCD3', 'congenital bile acid synthesis defect type 5']",0111066,616278,,,,,,,,,,
mondo:0014565,cataract 43,"['cataract 43', 'CTRCT43', 'cataract type 43', 'early-onset non-syndromic cataract caused by mutation in UNC45B', 'UNC45B early-onset non-syndromic cataract']",0110259,616279,98991,C4225389,,,,,,,,
mondo:0014566,Charcot-Marie-Tooth disease axonal type 2U,"['CMT2U', 'autosomal dominant Charcot-Marie-Tooth disease type 2U', 'autosomal dominant Charcot-Marie-Tooth disease type 2 due to MARS mutation', 'Charcot-Marie-Tooth disease type 2 caused by mutation in MARS', 'Charcot-Marie-Tooth disease, axonal, type 2U', 'MARS Charcot-Marie-Tooth disease type 2', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2U', 'Charcot-Marie-Tooth neuropathy type 2U', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2U', 'Charcot-Marie-Tooth neuropathy, type 2U']",0110173,616280,397735,C4084821,"['0.0937', '0.11273', '0.2257', '-0.01421', '0.001408', '-0.2983', '0.1086', '0.7944', '-0.6357', '-0.3342', '0.0076', '0.589', '-0.66', '0.3694', '-0.02126', '-0.3054', '-0.4995', '-0.442', '-0.668', '-0.506', '0.1436', '0.298', '0.244', '0.5767', '0.1693', '0.3938', '0.02197', '0.2445', '0.1562', '-0.07306', '0.516', '-0.42', '-0.08325', '0.02687', '0.288', '-0.7417', '-0.5293', '-0.1572', '0.5747', '-0.0787', '-1.034', '-0.444', '-0.457', '0.586', '-0.5757', '-0.2651', '0.2145', '-0.007786', '0.02481', '-0.01153', '0.1123', '0.533', '-0.3782', '-1.037', '0.2347', '0.002441', '-0.1484', '0.1375', '-0.8857', '-0.1722', '-0.5137', '0.011055', '0.6694', '0.2786', '-0.9424', '0.8784', '-0.02544', '0.6704', '-0.8145', '0.4001', '-0.7637', '0.008896', '0.674', '-0.1443', '1.478', '0.5386', '-0.3982', '0.497', '0.11224', '-0.5796', '-0.2188', '-0.2498', '1.124', '0.512', '0.1616', '0.1186', '0.2534', '0.609', '0.707', '0.03708', '0.0713', '-0.0871', '-0.06885', '0.262', '0.4895', '0.0523', '0.7476', '-0.539', '-0.2004', '0.8525']",,,,,,,
mondo:0014567,glutamate pyruvate transaminase 2 deficiency,"['GPT2 deficiency', 'MRT49', 'mental retardation, autosomal recessive type 49', 'mental retardation, autosomal recessive 49', 'postnatal microcephaly-infantile hypotonia-spastic diplegia-dysarthria-intellectual disability syndrome', 'neurodevelopmental disorder with microcephaly and spastic paraplegia']",,616281,477673,,,,,,,,,
mondo:0014568,hereditary spastic paraplegia 73,"['CPT1C autosomal dominant pure spastic paraplegia', 'hereditary spastic paraplegia type 73', 'autosomal dominant spastic paraplegia 73', 'autosomal dominant spastic paraplegia type 73', 'SPG73', 'spastic paraplegia 73, autosomal dominant', 'autosomal dominant pure spastic paraplegia caused by mutation in CPT1C']",0110818,616282,444099,C4225387,,,,,,,,
mondo:0014569,lethal congenital contracture syndrome 7,"['LCCS7', 'lethal congenital contracture syndrome type 7', 'CNTNAP1 lethal congenital contracture syndrome', 'lethal congenital contracture syndrome caused by mutation in CNTNAP1', 'lethal congenital contracture syndrome 7']",,616286,,C4225386,,,,,,,,
mondo:0014570,lethal congenital contracture syndrome 8,"['lethal congenital contracture syndrome 8', 'lethal congenital contracture syndrome caused by mutation in ADCY6', 'LCCS8', 'lethal congenital contracture syndrome type 8', 'ADCY6 lethal congenital contracture syndrome']",,616287,,C4225385,,,,,,,,
mondo:0014571,optic atrophy 9,"['autosomal recessive isolated optic atrophy caused by mutation in ACO2', 'ACO2 autosomal recessive isolated optic atrophy', 'OPA9', 'optic atrophy 9']",0111442,616289,,C4085249,,,,,,,,
mondo:0014572,Lichtenstein-Knorr syndrome,"['progressive autosomal recessive ataxia-deafness syndrome', 'spinocerebellar ataxia, autosomal recessive 19', 'autosomal recessive spinocerebellar ataxia 19', 'autosomal recessive spinocerebellar ataxia type 19', 'Lichtenstein-Knorr syndrome', 'progressive autosomal recessive ataxia-sensorineural hearing loss syndrome', 'SCAR19', 'LIKNS']",0080065,616291,448251,C4225383,"['-0.009285', '0.001913', '-0.003967', '0.002619', '0.00947', '-0.003664', '-0.00429', '0.01633', '-0.014565', '-0.00519', '0.00456', '0.009125', '-0.0006', '0.0007763', '-0.00847', '-0.010925', '-0.00747', '0.00267', '-0.005226', '-0.01651', '0.004967', '-0.007835', '0.001732', '-0.0122', '-0.001289', '-0.00475', '-0.00424', '-0.011604', '-0.004692', '0.000541', '0.00498', '0.001281', '0.002512', '0.01204', '-0.00734', '-0.00834', '-3.976e-05', '-0.01002', '-0.00998', '-0.01236', '0.00809', '-0.01546', '0.01075', '-0.00799', '-0.003885', '-0.01703', '-0.00873', '0.01324', '-0.0004897', '0.01071', '0.001726', '-0.007355', '-0.00348', '0.0076', '-0.004948', '-0.013855', '0.004158', '0.002644', '-0.01636', '0.003729', '0.01101', '0.010826', '0.004063', '0.00876', '0.00862', '0.01051', '0.00807', '0.01371', '-0.01094', '0.003782', '-0.002232', '0.00069', '0.0056', '-0.00992', '0.01458', '-0.002584', '-0.006683', '0.002354', '-0.0126', '-0.00873', '-0.0007954', '0.003345', '-0.004295', '0.006714', '-0.009415', '-0.00992', '0.0123', '0.0125', '0.01952', '-0.003767', '0.000956', '0.01633', '0.00505', '-0.004093', '0.00853', '0.007565', '0.000497', '-0.00444', '-0.008354', '-0.004883']",,,,,,,
mondo:0014573,Cole-Carpenter syndrome 2,"['Cole-Carpenter syndrome caused by mutation in SEC24D', 'CLCRP2', 'COLE-CARPENTER syndrome 2', 'Cole-Carpenter syndrome type 2', 'Cole-Carpenter syndrome 2', 'SEC24D Cole-Carpenter syndrome']",,616294,,C4225382,,,,,,,,
mondo:0014574,peeling skin-leukonuchia-acral punctate keratoses-cheilitis-knuckle pads syndrome,"['peeling skin with leukonychia, acral punctate keratoses, cheilitis, and knuckle pads', 'plack', 'plack syndrome', 'peeling skin-leukonychia-acral punctate keratoses-cheilitis-knuckle pads syndrome']",,616295,444138,C4225381,,,,,,,,
mondo:0014575,Singleton-Merten syndrome 2,"['DDX58 singleton-Merten dysplasia', 'singleton-Merten dysplasia caused by mutation in DDX58', 'SGMRT2', 'singleton-Merten syndrome type 2', 'singleton-Merten syndrome 2']",,616298,,C4225380,,,,,,,,
mondo:0014576,lipoyl transferase 1 deficiency,"['lipoyltransferase 1 deficiency', 'LIPT1D']",,616299,401862,C4225379,"['-0.3667', '0.3792', '0.1482', '-0.429', '-0.2303', '-0.316', '-0.02144', '0.4182', '-0.4749', '0.2607', '-0.4702', '-0.2059', '0.02396', '-0.1478', '0.08453', '0.1098', '0.1407', '-0.03076', '-0.04065', '-0.8677', '0.0685', '-0.2012', '0.2251', '0.1272', '-0.05643', '0.02258', '0.2834', '0.127', '-0.2393', '-0.205', '-0.0535', '0.2869', '0.56', '0.2491', '-0.2686', '-0.1152', '-0.28', '-0.0907', '-0.146', '0.01578', '-0.02411', '-0.3757', '-0.0747', '0.2876', '-0.288', '-0.0719', '0.04593', '0.11255', '-0.2634', '0.503', '-0.3616', '0.369', '-0.0682', '-0.323', '-0.02403', '-0.1035', '0.1501', '-0.2318', '-0.05402', '0.09973', '-0.01532', '0.1871', '0.2253', '-0.0678', '-0.3708', '-0.1682', '0.4536', '0.3105', '-0.4944', '0.1947', '-0.2313', '0.2966', '-0.1339', '-0.2913', '0.1227', '0.09406', '0.3315', '-0.04114', '0.08264', '0.0739', '0.1995', '-0.2042', '0.2476', '0.1271', '0.242', '0.3213', '-0.0576', '0.3767', '0.3972', '0.06964', '0.491', '0.3303', '0.0317', '0.07306', '0.5366', '0.651', '0.1776', '0.09247', '0.1917', '0.4573']",,,,,,,
mondo:0014577,short-rib thoracic dysplasia 13 with or without polydactyly,"['SRTD13', 'short-rib thoracic dysplasia 13 with or without polydactyly']",0110093,616300,,C4225378,,,,,,,,
mondo:0014578,congenital myasthenic syndrome 17,"['CMS17', 'congenital myasthenic syndrome caused by mutation in LRP4', 'LRP4 congenital myasthenic syndrome', 'congenital myasthenic syndrome type 17', 'myasthenic syndrome, congenital, type 17', 'myasthenic syndrome, congenital, 17']",0110674,616304,,C4225377,,,,,,,,
mondo:0014579,Senior-Loken syndrome 8,"['Senior-Loken syndrome type 8', 'WDR19 Senior-Loken syndrome', 'SENIOR-Loken syndrome 8', 'SLSN8', 'Senior-Loken syndrome 8', 'Senior-Loken syndrome caused by mutation in WDR19']",,616307,,C4225376,,,,,,,,
mondo:0014580,"intellectual disability, autosomal dominant 33","['mental retardation, autosomal dominant type 33', 'MRD33', 'autosomal dominant mental retardation 33', 'autosomal dominant intellectual disability 33', 'DPP6 autosomal dominant non-syndromic intellectual disability', 'autosomal dominant non-syndromic intellectual disability caused by mutation in DPP6', 'mental retardation, autosomal dominant 33', 'autosomal dominant non-syndromic intellectual disability 33', 'intellectual disability, autosomal dominant 33', 'intellectual disability, autosomal dominant type 33']",0070063,616311,2514,,,,,,,,,
mondo:0014581,congenital myasthenic syndrome 2A,"['myasthenic syndrome, congenital, slow-channel', 'congenital myasthenic syndrome 2A slow-channel', 'CMS IIa', 'myasthenic syndrome, congenital, 2A, slow-channel', 'myasthenic syndrome, congenital, postsynaptic slow-channel', 'slow channel congenital myasthenic syndrome', 'CMS2A', 'SCCMS', 'myasthenic syndrome, congenital, type IIa', 'congenital myasthenic syndrome type 2A']",0110681,616313,,C4225374,,,,,,,,
mondo:0014582,congenital myasthenic syndrome 2C,"['myasthenic syndrome, congenital, 2C, associated with acetylcholine receptor deficiency', 'congenital myasthenic syndrome 2C associated with acetylcholine receptor deficiency', 'congenital myasthenic syndrome type 2C', 'CMS2C']",0110680,616314,,C4225373,,,,,,,,
mondo:0014583,congenital myasthenic syndrome 3A,"['congenital myasthenic syndrome 3A, slow-channel', 'congenital myasthenic syndrome type 3A', 'CMS3A', 'myasthenic syndrome, congenital, 3A, slow-channel']",0110666,616321,,C4225372,,,,,,,,
mondo:0014584,congenital myasthenic syndrome 3B,"['CMS3B', 'congenital myasthenic syndrome type 3B', 'myasthenic syndrome, congenital, 3B, FAST-channel', 'congenital myasthenic syndrome 3B, fast-channel']",0110665,616322,,C4225371,,,,,,,,
mondo:0014585,congenital myasthenic syndrome 3C,"['congenital myasthenic syndrome 3C associated with acetylcholine receptor deficiency', 'myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency', 'congenital myasthenic syndrome type 3C', 'CMS3C']",0110664,616323,,C4225370,,,,,,,,
mondo:0014586,congenital myasthenic syndrome 4B,"['congenital myasthenic syndrome type 4B', 'CMS4B', 'congenital myasthenic syndrome 4B fast-channel', 'myasthenic syndrome, congenital, 4B, FAST-channel']",0110677,616324,,C4225369,,,,,,,,
mondo:0014587,congenital myasthenic syndrome 9,"['congenital myasthenic syndrome 9, associated with acetylcholine receptor deficiency', 'congenital myasthenic syndrome type 9', 'MUSK congenital myasthenic syndrome', 'congenital myasthenic syndrome caused by mutation in MUSK', 'myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency', 'CMS9']",0110670,616325,,C4225368,,,,,,,,
mondo:0014588,congenital myasthenic syndrome 11,"['congenital myasthenic syndrome 11 associated with acetylcholine receptor deficiency', 'Cms Ie, formerly', 'CMS11', 'CMS1E', 'congenital myasthenic syndrome caused by mutation in RAPSN', 'myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency', 'Cms Ie', 'CMS Ie', 'RAPSN congenital myasthenic syndrome', 'congenital myasthenic syndrome type 11', 'congenital myasthenic syndrome 1e', 'myasthenic syndrome, congenital, Ie', 'myasthenic syndrome, congenital, Ie, formerly']",0110675,616326,,,,,,C563831,,,,
mondo:0014589,maturity-onset diabetes of the young type 13,"['maturity-onset diabetes of the young, type 13', 'KCNJ11 maturity-onset diabetes of the young (disease)', 'MODY13', 'MODY type 13', 'MODY, type 13']",0111110,616329,,C4225365,,,,,,,,
mondo:0014590,congenital myasthenic syndrome 18,"['congenital myasthenic syndrome caused by mutation in SNAP25', 'myasthenic syndrome, congenital, 18', 'congenital myasthenic syndrome type 18', 'myasthenic syndrome, congenital, type 18', 'CMS18', 'myasthenic syndrome, congenital, 18, with intellectual disability and ataxia', 'SNAP25 congenital myasthenic syndrome']",0110683,616330,,C4225364,,,,,,,,
mondo:0014591,autosomal dominant Robinow syndrome 2,"['autosomal dominant Robinow syndrome caused by mutation in DVL1', 'DVL1 autosomal dominant Robinow syndrome', 'DRS2', 'Robinow syndrome, autosomal dominant type 2', 'autosomal dominant Robinow syndrome type 2', 'Robinow syndrome, autosomal dominant 2']",0060765,616331,,C4225363,,,,,,,,
mondo:0014592,microcephaly and chorioretinopathy 3,"['microcephaly and chorioretinopathy, autosomal recessive, type 3', 'microcephaly and chorioretinopathy type 3', 'microcephaly and chorioretinopathy, autosomal recessive, 3', 'TUBGCP4 microcephaly and chorioretinopathy', 'MCCRP3', 'microcephaly and chorioretinopathy caused by mutation in TUBGCP4']",0080107,616335,,C4225362,,,,,,,,
mondo:0014593,"developmental and epileptic encephalopathy, 29","['EIEE29', 'early infantile epileptic encephalopathy caused by mutation in AARS', 'developmental and epileptic encephalopathy 29', 'epileptic encephalopathy, early infantile, 29', 'epileptic encephalopathy, early infantile, type 29', 'DEE29', 'AARS early infantile epileptic encephalopathy']",0080451,616339,,C4225361,,,,,,,,
mondo:0014594,autosomal dominant nonsyndromic hearing loss 67,"['autosomal dominant deafness 67', 'OSBPL2 autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness 67', 'autosomal dominant nonsyndromic deafness caused by mutation in OSBPL2', 'deafness, autosomal dominant 67', 'DFNA67', 'autosomal dominant nonsyndromic deafness type 67', 'deafness, autosomal dominant type 67']",0110588,616340,,C4084712,,,,,,,,
mondo:0014595,"developmental and epileptic encephalopathy, 30","['SIK1 early infantile epileptic encephalopathy', 'early infantile epileptic encephalopathy caused by mutation in SIK1', 'epileptic encephalopathy, early infantile, 30', 'DEE30', 'epileptic encephalopathy, early infantile, type 30', 'developmental and epileptic encephalopathy 30', 'EIEE30']",0080465,616341,,C4225360,,,,,,,,
mondo:0014596,lissencephaly 7 with cerebellar hypoplasia,"['lissencephaly 7 with cerebellar hypoplasia', 'LIS7']",0112231,616342,,C4225359,,,,,,,,
mondo:0014597,immunodeficiency 39,"['primary immunodeficiency disease caused by mutation in IRF7', 'immunodeficiency 39', 'immunodeficiency type 39', 'IRF7 primary immunodeficiency disease', 'IMD39']",0111969,616345,,C4225358,,,,,,,,
mondo:0014598,"developmental and epileptic encephalopathy, 31","['early infantile epileptic encephalopathy caused by mutation in DNM1', 'DNM1 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 31', 'epileptic encephalopathy, early infantile, type 31', 'developmental and epileptic encephalopathy 31', 'DEE31', 'EIEE31']",0080437,616346,,C4225357,,,,,,,,
mondo:0014599,"intellectual disability, autosomal dominant 34","['autosomal dominant non-syndromic intellectual disability 34', 'autosomal dominant intellectual disability 34', 'autosomal dominant non-syndromic intellectual disability caused by mutation in COL4A3BP', 'COL4A3BP autosomal dominant non-syndromic intellectual disability', 'mental retardation, autosomal dominant 34', 'MRD34', 'intellectual disability, autosomal dominant type 34', 'mental retardation, autosomal dominant type 34', 'autosomal dominant mental retardation 34', 'intellectual disability, autosomal dominant 34', 'intellectual developmental disorder, autosomal dominant 34']",0070064,616351,,,,,,,,,,
mondo:0014600,"dyskeratosis congenita, autosomal recessive 6","['PARN dyskeratosis congenita', 'dyskeratosis congenita, autosomal recessive 6', 'dyskeratosis congenita, autosomal recessive type 6', 'autosomal recessive dyskeratosis congenita 6', 'DKCB6', 'dyskeratosis congenita caused by mutation in PARN']",0070024,616353,3322,C4225356,,C176929,,,,,,
mondo:0014601,autosomal recessive spinocerebellar ataxia 20,"['intellectual disability-coarse face-macrocephaly-cerebellar hypotrophy syndrome', 'autosomal recessive cerebellar ataxia caused by mutation in SNX14', 'spinocerebellar ataxia, autosomal recessive 20', 'SNX14 autosomal recessive cerebellar ataxia', 'autosomal recessive spinocerebellar ataxia type 20', 'spinocerebellar ataxia, autosomal recessive type 20', 'intellectual disability-coarse face-macrocephaly-cerebellar hypoplasia syndrome', 'SCAR20']",0080066,616354,397709,C4225355,"['-0.1092', '-0.3394', '0.10205', '0.03093', '-0.1166', '-0.9053', '0.1965', '0.0613', '-0.641', '-0.8545', '0.0915', '0.1815', '-0.1498', '0.10126', '0.513', '-0.3271', '-0.0734', '-0.1371', '0.08264', '-0.897', '-0.06415', '-0.2031', '0.1144', '-0.6787', '0.492', '-0.575', '-0.2069', '0.1433', '-0.1614', '-0.729', '0.03079', '0.3772', '-0.4019', '-0.09076', '0.4246', '0.10614', '-0.2915', '0.00322', '0.4585', '0.426', '0.3184', '0.09186', '-0.3225', '0.5396', '0.585', '-0.5522', '0.2966', '0.461', '0.4087', '-0.03818', '-0.3171', '0.1597', '-0.00976', '-0.3474', '-0.1044', '-0.812', '0.2192', '0.464', '-0.05643', '0.623', '-0.566', '0.2382', '0.2433', '-0.2406', '-0.4587', '0.5425', '0.2546', '0.5522', '-0.5903', '0.5264', '0.841', '0.654', '0.06027', '-0.798', '0.608', '0.2954', '0.359', '0.304', '0.1705', '0.4365', '-0.3896', '-0.659', '0.1895', '0.707', '-0.1548', '-0.633', '0.2422', '-0.06433', '0.4067', '0.603', '0.3906', '0.4998', '0.10815', '0.09796', '1.002', '1.007', '0.3403', '0.1625', '-0.3577', '0.00931']",,,,,,,
mondo:0014602,intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome,"['mental retardation, autosomal dominant type 35', 'autosomal dominant non-syndromic intellectual disability 35', 'intellectual disability, autosomal dominant type 35', 'mental retardation, autosomal dominant 35', 'intellectual disability, autosomal dominant 35', 'MRD35', 'autosomal dominant intellectual disability 35', 'autosomal dominant mental retardation 35']",0070065,616355,457279,C4225354,,,,,,,,
mondo:0014603,autosomal dominant nonsyndromic hearing loss 40,"['deafness, autosomal dominant 40', 'autosomal dominant nonsyndromic deafness caused by mutation in CRYM', 'autosomal dominant nonsyndromic deafness 40', 'autosomal dominant deafness 40', 'autosomal dominant nonsyndromic deafness type 40', 'deafness, autosomal dominant type 40', 'CRYM autosomal dominant nonsyndromic deafness', 'DFNA40']",0110566,616357,,C4084708,,,,,,,,
mondo:0014604,Parkinson disease 21,"['Parkinson disease type 21', 'hereditary late onset Parkinson disease caused by mutation in DNAJC13', 'Parkinson disease 21', 'PARK21', 'DNAJC13 hereditary late onset Parkinson disease']",0111251,616361,,C4225353,,,,,,,,
mondo:0014605,microcephaly-corpus callosum hypoplasia-intellectual disability-facial dysmorphism syndrome,"['mental retardation, autosomal dominant 36', 'intellectual disability, autosomal dominant type 36', 'mental retardation, autosomal dominant type 36', 'MRD36', 'autosomal dominant non-syndromic intellectual disability 36', 'intellectual disability, autosomal dominant 36', 'autosomal dominant mental retardation 36', 'autosomal dominant intellectual disability 36']",0070066,616362,457284,,,,,,,,,
mondo:0014606,intellectual disability-microcephaly-strabismus-behavioral abnormalities syndrome,"['intellectual disability, autosomal dominant 37', 'mental retardation, autosomal dominant 37', 'mental retardation, autosomal dominant type 37', 'White-Sutton syndrome', 'autosomal dominant intellectual disability 37', 'MRD37', 'autosomal dominant mental retardation 37', 'intellectual disability, autosomal dominant type 37', 'WHITE-Sutton syndrome', 'WHSUS']",0070067,616364,468678,,,,0009079,,,,,
mondo:0014607,"developmental and epileptic encephalopathy, 32","['early infantile epileptic encephalopathy caused by mutation in KCNA2', 'epileptic encephalopathy, early infantile, type 32', 'KCNA2 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 32', 'developmental and epileptic encephalopathy 32', 'DEE32', 'EIEE32']",0080416,616366,,C4225350,,,,,,,,
mondo:0014608,mandibulofacial dysostosis with alopecia,"['MFDA', 'mandibulofacial dysostosis with alopecia']",0060365,616367,443995,C4225349,"['-0.04437', '0.063', '0.04498', '-0.0249', '0.0402', '-0.0562', '0.02028', '0.06177', '-0.0506', '-0.04297', '-0.02145', '-0.003695', '-0.0234', '-0.005653', '-0.02756', '-0.01898', '0.0307', '-0.02353', '-0.02458', '-0.12427', '-0.03085', '0.006138', '0.04654', '-0.031', '0.02304', '9.92e-05', '-0.02583', '-0.01683', '0.01724', '-0.0288', '0.04892', '-0.007225', '0.0529', '0.02165', '0.00849', '-0.03268', '-0.01101', '-0.01732', '-0.03546', '-0.0791', '0.02005', '-0.05746', '0.0342', '-0.03925', '0.004944', '-0.0563', '-0.02786', '0.0538', '-0.01114', '0.01138', '-0.03482', '0.000601', '0.02296', '0.0243', '-0.0379', '-0.0473', '0.02228', '-0.04654', '-0.08575', '0.01717', '0.04642', '0.01764', '-0.004025', '0.02518', '0.01474', '0.000784', '0.07074', '0.0485', '-0.05112', '0.06586', '-0.0775', '-0.007275', '0.03873', '-0.04068', '0.01639', '0.0424', '0.02534', '-0.031', '-0.03488', '-0.02856', '0.00894', '0.002487', '-0.00924', '0.0916', '0.003042', '0.00778', '-0.00217', '0.06223', '0.06274', '0.0338', '0.0365', '0.05768', '0.003246', '0.00952', '0.1219', '0.00903', '0.0674', '-0.0973', '0.05295', '0.03137']",,,,,,,
mondo:0014609,cognitive impairment - coarse facies - heart defects - obesity - pulmonary involvement - short stature - skeletal dysplasia syndrome,"['CHOPS syndrome', 'CHOPS', 'cognitive impairment, coarse facies, heart defects, obesity, pulmonary involvement, short stature, and skeletal dysplasia']",,616368,444077,C4085597,"['-0.2311', '0.435', '0.1824', '0.784', '-0.1437', '-0.5044', '0.1769', '0.5625', '-0.2313', '-0.5146', '0.005978', '0.4502', '0.0696', '0.3203', '-0.994', '-0.1522', '-0.2654', '0.9277', '-0.5894', '-0.5796', '0.11395', '-0.0908', '0.08514', '-0.1311', '0.2014', '0.1775', '-0.4868', '-0.3274', '0.3376', '-0.305', '0.3552', '-0.667', '0.462', '-0.1279', '0.03775', '-0.3833', '-0.673', '-0.05338', '0.3948', '0.000741', '0.3142', '0.0499', '-0.711', '0.357', '0.002485', '-0.7207', '0.7812', '0.2712', '0.3064', '0.08746', '-0.6445', '-0.2075', '0.3396', '-0.317', '-0.2896', '0.341', '-0.5117', '-0.0935', '0.1328', '-0.359', '0.4993', '0.3965', '-0.306', '-0.536', '-0.05734', '0.691', '-0.3623', '0.4636', '0.3184', '0.726', '0.09656', '0.663', '0.1802', '-0.1951', '0.2201', '-0.4812', '0.04495', '-0.3403', '-1.35', '0.4268', '0.0482', '0.8726', '-0.0672', '0.193', '0.5874', '0.8354', '0.02641', '0.194', '0.701', '0.7104', '-0.05954', '0.448', '-0.08575', '0.6035', '0.811', '0.1842', '0.2233', '-0.3936', '-0.2795', '-0.05298']",,0009031,,,,,
mondo:0014611,multiple mitochondrial dysfunctions syndrome 4,"['multiple mitochondrial dysfunctions syndrome type 4', 'multiple mitochondrial dysfunctions syndrome 4', 'fatal multiple mitochondrial dysfunctions syndrome caused by mutation in ISCA2', 'ISCA2 fatal multiple mitochondrial dysfunctions syndrome', 'MMDS4']",0080136,616370,457406,C4225348,"['-0.03885', '0.04962', '0.002567', '-0.00481', '0.01494', '-0.05426', '0.01741', '0.0715', '-0.0703', '-0.02547', '-0.004158', '-0.00916', '0.006145', '-0.002386', '-0.02235', '-0.0557', '-0.01415', '-0.014595', '-0.02638', '-0.1016', '0.003645', '-0.0298', '0.0648', '-0.02577', '0.01233', '-0.00468', '-0.02107', '-0.011375', '-0.003819', '-0.02577', '0.0627', '-0.0004194', '0.07556', '0.01582', '0.01151', '-0.05084', '-0.01749', '-0.01021', '-0.01585', '-0.02592', '0.02238', '-0.0858', '0.02469', '-0.01804', '-0.005535', '-0.0696', '-0.02017', '0.0492', '0.01401', '0.008804', '-0.0413', '-0.01287', '0.00646', '-0.0135', '-0.0287', '-0.04138', '0.0564', '-0.00942', '-0.056', '-0.0010805', '0.0491', '0.01076', '0.007526', '0.01602', '-0.00953', '-0.0037', '0.067', '0.06573', '-0.05267', '0.05283', '-0.02748', '0.001763', '0.01246', '-0.0384', '0.012566', '0.03903', '0.004105', '0.003044', '-0.04156', '-0.01616', '-0.00506', '0.00864', '-0.015', '0.03793', '-0.004135', '0.002869', '0.04214', '0.05728', '0.076', '0.0003693', '0.02885', '0.03275', '0.00923', '-0.00981', '0.1192', '0.03778', '0.05307', '-0.077', '-0.007553', '0.0129']",,,,,,,
mondo:0014612,"pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4","['pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 4', 'PARN pulmonary fibrosis and/or bone marrow failure, Telomere-related', 'PFBMFT4', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related, 4', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in PARN', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 4']",,616371,,C4225347,,,,,,,,
mondo:0014613,"pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3","['RTEL1 pulmonary fibrosis and/or bone marrow failure, Telomere-related', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in RTEL1', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related, 3', 'pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 3', 'PFBMFT3', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 3']",,616373,,C4225346,,,,,,,,
mondo:0014614,congenital stationary night blindness 1G,"['congenital stationary night blindness type 1G', 'night blindness, congenital stationary, type 1G', 'CSNB1G']",0110714,616389,,C4225345,,,,,,,,
mondo:0014615,"trichothiodystrophy 2, photosensitive","['trichothiodystrophy 2, photosensitive', 'TTD2']",0111869,616390,,C4225344,,C173103,,,,,,
mondo:0014617,"intellectual disability, autosomal dominant 38","['autosomal dominant intellectual disability 38', 'EEF1A2 autosomal dominant non-syndromic intellectual disability', 'intellectual disability, autosomal dominant 38', 'psychomotor retardation, epilepsy, and language disability syndrome', 'intellectual disability, autosomal dominant type 38', 'PRELDS', 'MRD38', 'autosomal dominant mental retardation 38', 'mental retardation, autosomal dominant 38', 'autosomal dominant non-syndromic intellectual disability caused by mutation in EEF1A2', 'mental retardation, autosomal dominant type 38', 'autosomal dominant non-syndromic intellectual disability 38']",0070068,616393,,C4225343,,,,,,,,
mondo:0014618,retinitis pigmentosa 71,"['IFT172 retinitis pigmentosa', 'retinitis pigmentosa type 71', 'retinitis pigmentosa 71', 'retinitis pigmentosa caused by mutation in IFT172', 'RP71']",0110363,616394,,C4225342,,,,,,H35.5,,
mondo:0014619,"trichothiodystrophy 3, photosensitive","['trichothiodystrophy 3, photosensitive', 'trichothiodystrophy, complementation group A', 'TTD3']",0111871,616395,,C4017171,,C173099,,,,,,
mondo:0014620,myoclonic dystonia 26,"['KCTD17 myoclonus-dystonia syndrome', 'myoclonic dystonia type 26', 'dystonia 26, myoclonic', 'myoclonus-dystonia syndrome caused by mutation in KCTD17', 'DYT26']",0090036,616398,,C4225341,,,,,,,,
mondo:0014621,Brugada syndrome 9,"['KCND3 Brugada syndrome', 'BRGDA9', 'Brugada syndrome caused by mutation in KCND3', 'Brugada syndrome 9', 'Brugada syndrome type 9']",0110226,616399,,C4225340,,,,,,,,
mondo:0014622,isolated focal non-epidermolytic palmoplantar keratoderma,"['palmoplantar keratoderma, nonepidermolytic, focal 2', 'FNEPPK2', 'palmoplantar keratoderma, nonepidermolytic, focal type 2']",0111711,616400,448264,C4225339,,,,,,,,
mondo:0014623,"microcephaly 14, primary, autosomal recessive","['microcephaly 14, primary, autosomal recessive', 'autosomal recessive primary microcephaly caused by mutation in SASS6', 'MCPH14', 'SASS6 autosomal recessive primary microcephaly']",0070279,616402,,C4225338,,,,,,,,
mondo:0014624,Brown syndrome,"['tendon sheath adherence, Superior oblique', 'Brown^s tendon sheath syndrome', 'Brown tendon sheath syndrome', 'BRWNS', 'Brown syndrome', 'superior oblique tendon sheath syndrome', 'Brown^s (tendon) sheath syndrome', 'Brown^s sheath syndrome']",10235,616407,,C0155339,,,,,378.61,,,
mondo:0014625,"developmental and epileptic encephalopathy, 33","['EEF1A2 early infantile epileptic encephalopathy', 'developmental and epileptic encephalopathy 33', 'epileptic encephalopathy, early infantile, 33', 'epileptic encephalopathy, early infantile, type 33', 'EIEE33', 'DEE33', 'early infantile epileptic encephalopathy caused by mutation in EEF1A2']",0080463,616409,,C4225337,,,,,,,,
mondo:0014626,spinocerebellar ataxia type 41,"['spinocerebellar ataxia 41', 'SCA41', 'spinocerebellar ataxia type 41']",0111744,616410,458798,C4225158,"['-0.169', '-0.2612', '0.0002176', '0.2007', '-0.1354', '-1.026', '0.1953', '0.001668', '-0.6733', '-0.7466', '0.121', '0.2585', '-0.2067', '0.03458', '0.617', '-0.3591', '-0.265', '-0.266', '0.0704', '-0.9326', '-0.1296', '-0.3464', '0.1338', '-0.5186', '0.501', '-0.4946', '-0.3828', '0.1788', '-0.1764', '-0.824', '-0.05347', '0.4321', '-0.4844', '-0.2101', '0.3635', '0.2333', '-0.1896', '0.05283', '0.6514', '0.2776', '0.2035', '0.2107', '-0.482', '0.4807', '0.568', '-0.6387', '0.1261', '0.5513', '0.4028', '0.013214', '-0.1641', '0.203', '-0.02972', '-0.477', '-0.005665', '-0.912', '0.3667', '0.5605', '-0.1553', '0.52', '-0.5615', '0.298', '0.2472', '-0.2844', '-0.5386', '0.5654', '0.2712', '0.5166', '-0.6177', '0.5625', '0.9126', '0.588', '-0.0907', '-0.7744', '0.7134', '0.5635', '0.278', '0.3555', '0.2141', '0.4702', '-0.4558', '-0.8003', '0.2935', '0.8687', '-0.2996', '-0.601', '0.2756', '-0.08246', '0.482', '0.5693', '0.3252', '0.3638', '0.1302', '0.06696', '0.9854', '1.185', '0.3755', '0.3323', '-0.4058', '0.003506']",,0009058,,,,,
mondo:0014627,dystonia 27,"['dystonia 27', 'dystonia type 27', 'primary dystonia, DYT27 type', 'dystonic disorder caused by mutation in COL6A3', 'COL6A3 dystonic disorder', 'DYT27']",0090050,616411,464440,C4225336,,,,,,,,
mondo:0014628,"basal ganglia calcification, idiopathic, 6","['bilateral striopallidodentate calcinosis caused by mutation in XPR1', 'basal ganglia calcification, idiopathic, 6', 'XPR1 bilateral striopallidodentate calcinosis', 'basal ganglia calcification, idiopathic, type 6', 'IBGC6']",,616413,,C4225335,,,,,,,,
mondo:0014629,autoimmune interstitial lung disease-arthritis syndrome,"['copa defect', 'autoimmune interstitial lung, joint, and kidney disease', 'copa syndrome', 'AILJK']",0081242,616414,444092,C4225334,,,,,,,,
mondo:0014630,familial adenomatous polyposis 3,"['NTHL1-related AFAP', 'familial adenomatous polyposis type 3', 'FAP3', 'NTHL1-related attenuated FAP', 'NTHL1-related attenuated familial adenomatous polyposis', 'familial adenomatous polyposis 3']",0080411,616415,454840,C4225157,,,,,,,,
mondo:0014631,"hypomagnesemia, seizures, and intellectual disability","['hypomagnesemia, seizures, and mental retardation', 'hypomagnesemia, seizures, and intellectual disability', 'HOMGSMR']",,,,C4225333,,,,,,,,
mondo:0014632,hypomyelinating leukodystrophy 10,"['PYCR2 leukodystrophy', 'leukodystrophy, hypomyelinating, 10', 'hypomyelinating leukodystrophy type 10', 'HLD10', 'leukodystrophy, hypomyelinating, type 10', 'leukodystrophy caused by mutation in PYCR2']",0060788,616420,,C4225332,"['-0.05096', '0.09656', '0.0217', '-0.0227', '0.05838', '-0.0872', '-0.04507', '0.12', '-0.1037', '-0.01897', '-0.04025', '0.01484', '-0.0381', '-0.04163', '-0.001053', '-0.06476', '0.03833', '-0.08105', '-0.04517', '-0.1288', '0.00975', '-0.07715', '0.04453', '-0.0555', '0.03268', '-0.012024', '-0.04507', '-0.011795', '-0.00528', '-0.02956', '0.04758', '0.003344', '0.0877', '0.022', '0.0315', '-0.04468', '-0.053', '-0.0528', '-0.010315', '-0.0538', '0.0461', '-0.1326', '0.03128', '-0.04306', '-0.03555', '-0.07074', '-0.00968', '0.06836', '0.000789', '-0.00902', '0.05023', '-0.003536', '-0.05713', '-0.024', '-0.02702', '-0.034', '0.1213', '-0.06287', '-0.11554', '0.002623', '0.03017', '0.03558', '0.03812', '0.01715', '-0.04037', '-0.03644', '0.0856', '0.07666', '-0.09216', '0.0897', '-0.0717', '0.03995', '0.04178', '-0.0705', '0.05573', '0.04272', '0.01965', '0.03525', '-0.0626', '-0.0685', '0.01503', '-0.0284', '0.02481', '0.0849', '0.010376', '0.005856', '0.0226', '0.10455', '0.0681', '0.01137', '0.03427', '0.1048', '0.00565', '0.03894', '0.1737', '0.071', '0.07587', '-0.1162', '0.0224', '0.04468']",,,,,,,
mondo:0014633,myoclonic-atonic epilepsy,"['myoclonic-atonic epilepsy', 'mae']",0060475,616421,,C4085238,,,,,,,,
mondo:0014634,"46,XY sex reversal 10","['46XY sex reversal 10', '46,XY Sex reversal type 10', '46,XY sex reversal 10', 'SRXY10', 'chromosome 17Q24 deletion syndrome', '46,XY SEX reversal 10']",0111775,616425,,C4225331,,,,,,,,
mondo:0014635,"microphthalmia, isolated, with coloboma 10","['microphthalmia, isolated, with coloboma caused by mutation in RBP4', 'microphthalmia, isolated, with coloboma 10', 'MCOPCB10', 'RBP4 microphthalmia, isolated, with coloboma', 'microphthalmia, isolated, with coloboma type 10']",,616428,,C4225330,,,,,,,,
mondo:0014636,combined oxidative phosphorylation defect type 25,"['MARS2 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency caused by mutation in MARS2', 'combined oxidative phosphorylation deficiency 25', 'COXPD25', 'combined oxidative phosphorylation deficiency type 25']",0111468,616430,447954,C4225329,,,0009035,,,,,
mondo:0014637,DOCK2 deficiency,"['immunodeficiency 40', 'IMD40', 'immunodeficiency type 40']",0111951,616433,447737,C4225328,,,,,,,,
mondo:0014638,Fanconi anemia complementation group T,"['Fanconi anemia, complementation group T', 'UBE2T Fanconi anemia', 'Fanconi Anemia, complementation group type T', 'Fanconi anaemia complementation group type T', 'Fanconi anemia caused by mutation in UBE2T', 'FANCT', 'Fanconi anaemia caused by mutation in UBE2T', 'Fanconi anemia complementation group type T', 'UBE2T Fanconi anaemia']",0111081,616435,,C4084840,,,,,,,,
mondo:0014639,familial temporal lobe epilepsy 7,"['epilepsy, familial temporal lobe, 7', 'epilepsy, familial temporal lobe, type 7', 'familial temporal lobe epilepsy type 7', 'ETL7']",0060751,616436,,C4225327,,,,,,,,
mondo:0014640,frontotemporal dementia and/or amyotrophic lateral sclerosis 3,"['FTDALS3', 'frontotemporal dementia and/or amyotrophic lateral sclerosis type 3', 'frontotemporal dementia and/or amyotrophic lateral sclerosis 3']",0110068,616437,803,C4225326,,,,,,,,
mondo:0014641,frontotemporal dementia and/or amyotrophic lateral sclerosis 4,"['frontotemporal dementia and/or amyotrophic lateral sclerosis type 4', 'frontotemporal dementia and/or amyotrophic lateral sclerosis 4', 'FTDALS4']",0110069,616439,,C4225325,,,,,,,,
mondo:0014642,"candidiasis, familial, 9","['candidiasis, familial, type 9', 'candidiasis, familial, 9', 'CANDF9', 'IL17RC chronic mucocutaneous candidiasis (disease)']",,616445,,C4225324,,,,,,,,
mondo:0014643,congenital cataract-microcephaly-nevus flammeus simplex-severe intellectual disability syndrome,"['Basel-Vanagait-Smirin-Yosef syndrome', 'BASEL-Vanagaite-SMIRIN-YOSEF syndrome', 'BVSYS']",,616449,464738,C4225323,,,,,,,,
mondo:0014644,hereditary spastic paraplegia 74,"['IBA57 hereditary spastic paraplegia', 'SPG74', 'hereditary spastic paraplegia caused by mutation in IBA57', 'autosomal recessive spastic paraplegia 74', 'spastic paraplegia 74, autosomal recessive', 'autosomal recessive spastic paraplegia type 74', 'hereditary spastic paraplegia type 74']",0110819,616451,468661,C4225322,,,,,,,,
mondo:0014645,BENTA disease,"['BENTA', 'B-cell expansion with NFKB and T-cell anergy', 'B-cell expansion with NF-kB and T-cell anergy disease']",,616452,464336,CN242071,,,,,,,,
mondo:0014646,Zimmermann-Laband syndrome 2,"['ATP6V1B2 Zimmermann-Laband syndrome', 'Zimmermann-Laband syndrome caused by mutation in ATP6V1B2', 'Zimmermann-Laband syndrome type 2', 'Zimmermann-Laband syndrome 2', 'ZLS2']",,616455,,C4225321,,,,,,,,
mondo:0014647,"developmental and epileptic encephalopathy, 50","['epileptic encephalopathy, early infantile, 50', 'congenital disorder of glycosylation type 1z', 'congenital disorder of glycosylation, type Iz', 'EIEE50', 'CDG syndrome type Iz', 'DEE50', 'congenital disorder of glycosylation, type Iz, formerly', 'carbohydrate deficient glycoprotein syndrome type Iz', 'CAD-CDG', 'CDG1Z', 'CDG-Iz', 'developmental and epileptic encephalopathy 50']",0080419,616457,448010,C4225320,,,,,,,,
mondo:0014648,Al-Raqad syndrome,"['Al-Raqad syndrome', 'AL-RAQAD syndrome', 'ARS']",,616459,,C4085595,,,,,,,,
mondo:0014649,"intellectual disability, autosomal recessive 50","['intellectual disability, autosomal recessive 50', 'EDC3 autosomal recessive non-syndromic intellectual disability', 'MRT50', 'mental retardation, autosomal recessive 50', 'mental retardation, autosomal recessive type 50', 'autosomal recessive non-syndromic intellectual disability caused by mutation in EDC3', 'intellectual developmental disorder, autosomal recessive 50', 'intellectual disability, autosomal recessive type 50']",0081213,616460,,,,,,,,,,
mondo:0014650,familial temporal lobe epilepsy 8,"['familial temporal lobe epilepsy type 8', 'epilepsy, familial temporal lobe, type 8', 'ETL8', 'epilepsy, familial temporal lobe, 8']",0060754,616461,,C4225318,,,,,,,,
mondo:0014651,acrofacial dysostosis Cincinnati type,"['POLR1A acrofacial dysostosis', 'acrofacial dysostosis, Cincinnati type', 'AFDCIN', 'acrofacial dysostosis caused by mutation in POLR1A']",0060353,616462,,C4225317,,,,,,,,
mondo:0014652,exudative vitreoretinopathy 6,"['exudative vitreoretinopathy caused by mutation in ZNF408', 'exudative vitreoretinopathy 6', 'ZNF408 exudative vitreoretinopathy', 'EVR6', 'exudative vitreoretinopathy type 6']",0111410,616468,,C4225316,,,,,,,,
mondo:0014653,retinitis pigmentosa 72,"['retinitis pigmentosa type 72', 'retinitis pigmentosa 72', 'RP72', 'retinitis pigmentosa caused by mutation in ZNF408', 'ZNF408 retinitis pigmentosa']",0110395,616469,,C4225315,,,,,,H35.5,,
mondo:0014654,Ullrich congenital muscular dystrophy 2,"['Ullrich congenital muscular dystrophy caused by mutation in COL12A1', 'UCMD2', 'Ullrich congenital muscular dystrophy type 2', 'COL12A1 Ullrich congenital muscular dystrophy', 'Ullrich congenital muscular dystrophy 2']",,616470,,C4225314,,,,,,,,
mondo:0014656,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2","['progressive external ophthalmoplegia, autosomal recessive 2', 'progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RNASEH1', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 2', 'PEOB2', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 2', 'RNASEH1 progressive external ophthalmoplegia with mitochondrial DNA deletions']",0111515,616479,,C4225312,,,,,,,,
mondo:0014657,primary ciliary dyskinesia 32,"['ciliary dyskinesia, primary, type 32', 'primary ciliary dyskinesia type 32', 'RSPH3 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 32, without situs inversus', 'primary ciliary dyskinesia 32 without situs inversus', 'ciliary dyskinesia, primary, 32', 'CILD32', 'primary ciliary dyskinesia caused by mutation in RSPH3']",0110603,616481,,C4225311,,,,,,,,
mondo:0014658,severe achondroplasia-developmental delay-acanthosis nigricans syndrome,"['SADDAN dysplasia', 'severe achondroplasia with developmental delay and acanthosis nigricans', 'SADDAN', 'achondroplasia, severe, with developmental delay and acanthosis nigricans']",0111158,616482,85165,,"['0.09607', '0.3774', '0.1209', '-0.35', '0.2151', '-0.2803', '-0.47', '0.3972', '-0.49', '-0.974', '-0.0819', '0.7153', '-0.4412', '-0.10144', '-0.1335', '-0.0955', '0.0585', '0.1366', '-0.5884', '-0.3928', '0.6387', '-0.581', '-0.316', '-0.4626', '0.1725', '0.2227', '-0.1769', '-0.594', '0.4878', '-0.851', '0.6924', '-0.2598', '0.4316', '-0.638', '0.3193', '0.4167', '-0.5386', '0.0565', '0.1492', '-0.05457', '0.2135', '-0.666', '-0.3657', '0.3137', '-0.2036', '0.03165', '-0.0626', '0.0521', '0.202', '0.03723', '0.1464', '0.1744', '0.2637', '0.3254', '-0.1588', '0.3247', '-0.2417', '0.03378', '-0.493', '-0.08234', '0.1443', '-0.2502', '-0.4207', '-0.0877', '-0.3333', '0.3137', '0.1052', '-0.00416', '-0.9375', '0.648', '-0.03864', '0.5493', '0.3018', '0.1694', '-0.303', '0.029', '-0.1012', '0.529', '0.309', '-0.381', '0.2058', '0.3447', '-0.00971', '-0.6436', '-0.871', '0.518', '-0.02196', '0.347', '0.0788', '0.571', '0.377', '-0.0363', '0.2756', '-0.6353', '0.668', '-0.2272', '0.2148', '-0.523', '0.11224', '-0.03091']",,,,783.40,Q77.4,,
mondo:0014659,infantile liver failure syndrome 2,"['infantile liver failure syndrome 2', 'NBAS infantile liver failure', 'infantile liver failure caused by mutation in NBAS', 'infantile liver failure syndrome type 2', 'ILFS2']",,616483,,CN232144,"['-0.0368', '0.0953', '0.01093', '0.01851', '0.02216', '-0.1191', '0.00938', '0.1156', '-0.1029', '-0.0076', '-0.06824', '-0.05362', '0.002323', '0.01799', '-0.05777', '-0.0807', '-0.02954', '-0.03583', '-0.02264', '-0.186', '0.006058', '-0.08374', '0.1096', '-0.068', '0.01978', '-0.06104', '-0.005646', '-0.01215', '-0.02155', '-0.0532', '0.0673', '0.02498', '0.1415', '0.02841', '0.02695', '-0.003729', '-0.05328', '-0.03793', '-0.02434', '-0.0664', '-0.01408', '-0.0926', '0.0474', '0.01118', '-0.03796', '-0.0654', '-0.04666', '0.05835', '0.002642', '0.06415', '-0.03418', '0.02338', '0.03534', '0.004974', '-0.04443', '-0.07043', '0.0956', '-0.04922', '-0.1553', '0.01758', '0.05075', '0.0341', '0.01738', '-0.02364', '0.007774', '-0.0251', '0.12177', '0.09424', '-0.0957', '0.0947', '-0.08124', '0.0299', '0.02864', '-0.05783', '0.0335', '0.03079', '0.04892', '-0.02423', '-0.0504', '-0.03723', '0.003263', '0.006264', '-0.1107', '0.06073', '0.01666', '0.00363', '0.06836', '0.0919', '0.1251', '0.02467', '0.0849', '0.05615', '-0.03595', '0.01171', '0.1836', '0.094', '0.0937', '-0.1293', '0.0074', '0.0319']",C158135,,,,,,
mondo:0014660,"microcephaly 15, primary, autosomal recessive","['MCPH15', 'microcephaly 15, primary, autosomal recessive', 'neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities']",0070277,616486,,C4225310,,,,,,,,
mondo:0014661,epidermolysis bullosa simplex with nail dystrophy,"['epidermolysis bullosa simplex 5D, generalized intermediate, autosomal recessive', 'epidermolysis bullosa simplex 5D, generalised intermediate, autosomal recessive', 'EBSND', 'epidermolysis bullosa simplex with nail dystrophy']",,616487,,C4225309,,,,,,,,
mondo:0014662,congenital insensitivity to pain-hypohidrosis syndrome,"['hereditary sensory and autonomic neuropathy type VIII', 'neuropathy, hereditary sensory and autonomic, type VIII', 'HSAN8', 'neuropathy, hereditary sensory and autonomic, type 8', 'HSAN 8', 'CIP-hypohidrosis syndrome', 'hereditary sensory and autonomic neuropathy type 8']",0070153,616488,478664,C4225308,,,,,,,,
mondo:0014663,Silver-Russell syndrome 3,"['growth restriction, severe, with distinctive facies', 'GRDF', 'SRS3']",,616489,,C4225307,,,,,,,,
mondo:0014664,Joubert syndrome 23,"['Joubert syndrome caused by mutation in KIAA0586', 'JBTS23', 'Joubert syndrome 23', 'KIAA0586 Joubert syndrome', 'Joubert syndrome type 23']",0110992,616490,,C4084822,,,,,,,,
mondo:0014665,Charcot-Marie-Tooth disease axonal type 2V,"['autosomal dominant Charcot-Marie-Tooth disease type 2 due to NAGLU mutation', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2V', 'hereditary adult-onset painful axonal polyneuropathy', 'Charcot-Marie-Tooth neuropathy, type 2V', 'CMT2V', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2V', 'NAGLU Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth neuropathy type 2V', 'Charcot-Marie-Tooth disease, axonal, type 2V', 'autosomal dominant Charcot-Marie-Tooth disease type 2V', 'Charcot-Marie-Tooth disease caused by mutation in NAGLU']",0110178,616491,447964,C4225306,"['-0.00858', '0.06128', '0.02821', '-0.006195', '0.007416', '-0.0563', '-0.003498', '0.06165', '-0.05765', '-0.01654', '-0.01787', '0.01121', '-0.0001134', '0.01441', '-0.01486', '-0.0544', '0.001422', '-0.01727', '-0.004467', '-0.0864', '0.01119', '-0.01839', '0.02', '0.00591', '0.000431', '-0.00609', '-0.00239', '-0.004723', '0.004852', '-0.02754', '0.04556', '-0.01427', '0.0634', '0.007767', '0.043', '-0.0337', '-0.01993', '-0.01886', '0.006363', '-0.04144', '-0.03119', '-0.05667', '0.01747', '-0.00369', '-0.01706', '-0.04254', '-0.02702', '0.03433', '0.01013', '0.0186', '0.006435', '0.001264', '0.001247', '-0.02103', '-0.01761', '-0.04315', '0.0435', '-0.02083', '-0.0647', '-0.0004199', '0.02545', '-0.01387', '0.02411', '0.02684', '-0.00784', '0.02673', '0.04144', '0.03915', '-0.03885', '0.03108', '-0.04095', '-0.00218', '0.00863', '-0.03326', '0.04813', '0.0339', '-0.02025', '0.00609', '-0.02931', '-0.04486', '-0.013855', '-0.02016', '-0.013725', '0.04214', '-0.003366', '0.01028', '0.01413', '0.04132', '0.05133', '0.01366', '0.015564', '0.02293', '0.0373', '0.01256', '0.08405', '0.046', '0.03204', '-0.05014', '-0.03455', '0.01421']",,,,,,,
mondo:0014666,hypomyelinating leukodystrophy 11,"['leukodystrophy, hypomyelinating, 11', 'leukodystrophy, hypomyelinating, type 11', 'HLD11', 'hypomyelinating leukodystrophy type 11', 'POLR1C leukodystrophy', 'leukodystrophy caused by mutation in POLR1C']",0060792,616494,,C4225305,,,,,,,,
mondo:0014667,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3","['COA5 fatal infantile encephalocardiomyopathy', 'fatal infantile encephalocardiomyopathy caused by mutation in COA5', 'cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 3', 'CEMCOX3', 'mitochondrial complex IV, deficiency, nuclear type 9', 'cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 3']",0080359,616500,,C4225154,,,,,,,,
mondo:0014668,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4","['COA6 fatal infantile encephalocardiomyopathy', 'mitochondrial complex IV deficiency, nuclear type 13', 'cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 4', 'cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 4', 'CEMCOX4', 'fatal infantile encephalocardiomyopathy caused by mutation in COA6']",0080360,616501,,C4225304,,,,,,,,
mondo:0014669,cone-rod dystrophy 21,"['cone-rod dystrophy caused by mutation in DRAM2', 'CORD21', 'DRAM2 cone-rod dystrophy', 'retinal dystrophy with early macular involvement', 'cone-rod dystrophy 21', 'cone-rod dystrophy type 21']",,616502,,CN231743,,,,,,,,
mondo:0014670,lethal congenital contracture syndrome 9,"['LCCS9', 'lethal congenital contracture syndrome caused by mutation in ADGRG6', 'lethal congenital contracture syndrome 9', 'lethal congenital contracture syndrome type 9', 'ADGRG6 lethal congenital contracture syndrome']",,616503,,C4225303,,,,,,,,
mondo:0014671,"neuropathy, hereditary motor and sensory, type 6B","['HMSN 6B', 'neuropathy, hereditary motor and sensory, type VIB', 'SLC25A46 hereditary motor and sensory neuropathy type 6', 'CMT6B', 'Charcot-Marie-Tooth disease, type 6B', 'hereditary motor and sensory neuropathy type 6 caused by mutation in SLC25A46', 'HMSN6B']",,616505,,C4225302,"['-0.01402', '0.2021', '0.0949', '0.11237', '-0.0904', '-0.3198', '-0.1238', '0.249', '-0.383', '0.1306', '-0.0735', '0.04016', '-0.04242', '0.02002', '0.1719', '-0.1418', '-0.0942', '-0.0848', '0.0325', '-0.3335', '0.1598', '-0.12146', '0.02809', '0.1965', '0.0293', '0.06198', '0.0346', '-0.01471', '-0.1062', '-0.11774', '0.09015', '0.04807', '0.1968', '0.0143', '0.11725', '-0.2421', '-0.005665', '-0.193', '-0.04736', '-0.235', '-0.03772', '-0.254', '0.03235', '0.1997', '-0.10657', '-0.2922', '-0.04587', '0.1656', '0.0819', '0.04504', '-0.1006', '0.02283', '-0.1284', '0.01765', '-0.0341', '-0.143', '0.3286', '-0.04874', '-0.2373', '0.05563', '-0.0203', '-0.00817', '0.3425', '0.1162', '-0.04074', '0.29', '0.195', '0.314', '-0.1819', '0.132', '-0.2155', '0.0488', '0.0393', '-0.3345', '0.3647', '0.1023', '-0.06256', '0.175', '-0.10114', '-0.03888', '-0.0903', '-0.1356', '-0.03616', '0.3354', '-0.07117', '-0.1272', '0.10913', '0.2896', '0.2146', '0.1087', '0.1727', '-0.01898', '0.2036', '-0.1329', '0.463', '0.1687', '0.2478', '-0.2145', '-0.04385', '0.02342']",,0009075,,,,,
mondo:0014672,osteogenesis imperfecta type 17,"['osteogenesis imperfecta type XVII', 'osteogenesis imperfecta, type 17', 'OI17', 'osteogenesis imperfecta caused by mutation in SPARC', 'osteogenesis imperfecta, type XVII', 'SPARC osteogenesis imperfecta']",0110338,616507,216820,C4225301,,,,,,,,
mondo:0014673,cataract 44,"['cataract 44', 'LSS early-onset non-syndromic cataract', 'total early-onset cataract', 'CTRCT44', 'cataract type 44', 'early-onset non-syndromic cataract caused by mutation in LSS']",0110267,616509,98994,C4225300,,,,,,,,
mondo:0014674,maturity-onset diabetes of the young type 14,"['maturity-onset diabetes of the young, type 14', 'APPL1 maturity-onset diabetes of the young (disease)', 'MODY14']",0111111,616511,,C4225299,,,,,,,,
mondo:0014675,autosomal recessive nonsyndromic hearing loss 104,"['autosomal recessive deafness 104', 'autosomal recessive nonsyndromic deafness 104', 'deafness, autosomal recessive type 104', 'DFNB104', 'autosomal recessive nonsyndromic deafness type 104', 'deafness, autosomal recessive 104', 'RIPOR2 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness caused by mutation in RIPOR2']",0110465,616515,,C4225298,,,,,,,,
mondo:0014676,"Emery-Dreifuss muscular dystrophy 3, autosomal recessive","['EDMD3', 'Emery-Dreifuss muscular dystrophy 3, autosomal recessive', 'autosomal recessive Emery-Dreifuss muscular dystrophy caused by mutation in LMNA', 'EMERY-Dreifuss muscular dystrophy 3, autosomal recessive', 'LMNA autosomal recessive Emery-Dreifuss muscular dystrophy']",0070248,616516,,C2750035,,,,C567633,,,,
mondo:0014677,achromatopsia 7,"['achromatopsia type 7', 'ACHM7', 'achromatopsia 7', 'ATF6 achromatopsia', 'achromatopsia caused by mutation in ATF6']",0110009,616517,,C4225297,,,,,,,,
mondo:0014678,"intellectual disability, autosomal dominant 39","['autosomal dominant intellectual disability 39', 'mental retardation, autosomal dominant type 39', 'autosomal dominant mental retardation 39', 'MYT1L autosomal dominant non-syndromic intellectual disability', 'intellectual disability, autosomal dominant type 39', 'MRD39', 'chromosome 2P25.3 deletion syndrome', 'autosomal dominant non-syndromic intellectual disability 39', 'chromosome 2P25.3 Duplication syndrome', 'intellectual developmental disorder, autosomal dominant 39', 'intellectual disability, autosomal dominant 39', 'autosomal dominant non-syndromic intellectual disability caused by mutation in MYT1L', 'mental retardation, autosomal dominant 39']",0070069,616521,,C4225296,,,,,,,,
mondo:0014679,"polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis","['PMGYCHA', 'polymicrogyria, perisylvian, with cerebellar hypoplasia and arthrogryposis']",,616531,,C4225295,,,,,,,,
mondo:0014680,"herpes simplex encephalitis, susceptibility to, 7","['IRF3 herpes simplex encephalitis', 'herpes simplex encephalitis caused by mutation in IRF3', 'herpes simplex encephalitis, susceptibility to, 7', 'Herpes simplex encephalitis, susceptibility to, 5', 'encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 7', 'Herpes simplex encephalitis, susceptibility to, type 7', 'IIAE7', 'encephalopathy, acute, infection-induced, susceptibility to, 7', 'encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 7']",,616532,,,,,,,,,,
mondo:0014681,"thyroid cancer, nonmedullary, 4","['thyroid cancer, nonmedullary, 4', 'FOXE1 thyroid cancer, nonmedullary', 'thyroid cancer, nonmedullary, type 4', 'thyroid cancer, nonmedullary caused by mutation in FOXE1', 'NMTC4']",,616534,,C4225293,,,,,,,,
mondo:0014682,"thyroid cancer, nonmedullary, 5","['thyroid cancer, nonmedullary, 5', 'HABP2 thyroid cancer, nonmedullary', 'thyroid cancer, nonmedullary, type 5', 'NMTC5', 'thyroid cancer, nonmedullary caused by mutation in HABP2']",,616535,,C4225292,,,,,,,,
mondo:0014683,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A9","['MDDGA9', 'Walker-Warburg syndrome or muscle-eye brain disease, Dag1-related', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 9']",0111232,616538,899,C4225291,,,,,,,,
mondo:0014684,combined oxidative phosphorylation defect type 26,"['combined oxidative phosphorylation deficiency caused by mutation in TRMT5', 'combined oxidative phosphorylation deficiency type 26', 'combined oxidative phosphorylation deficiency 26', 'TRMT5 combined oxidative phosphorylation deficiency', 'COXPD26']",0111490,616539,477684,C4225290,"['-0.6685', '0.165', '0.005795', '-0.1809', '-0.2286', '-0.4016', '0.1932', '0.6343', '-0.4602', '0.014175', '-0.10565', '-0.263', '-0.0539', '-0.1827', '-0.01689', '0.01047', '-0.0519', '-0.1547', '-0.532', '-0.647', '0.725', '-0.2302', '0.3315', '0.2905', '0.05145', '0.04782', '0.1881', '0.006943', '-0.1399', '-0.2019', '0.2605', '0.1757', '0.703', '0.1925', '-0.1327', '-0.4102', '-0.1982', '-0.1006', '0.02274', '-0.0999', '0.1913', '-0.3152', '-0.11523', '0.656', '-0.4536', '-0.2051', '0.1392', '0.134', '-0.3782', '0.1323', '-0.289', '-0.04593', '0.0701', '-0.05917', '-0.06274', '-0.305', '0.331', '-0.02109', '0.01338', '0.1946', '-0.1442', '0.06714', '0.3196', '-0.06247', '-0.3535', '0.1384', '0.1442', '0.5664', '-0.361', '0.3162', '-0.2551', '0.373', '0.2134', '0.02567', '0.1733', '-0.08', '0.2257', '-0.3079', '0.03102', '0.359', '0.2708', '0.1317', '0.1274', '0.3025', '0.03482', '0.07794', '0.1448', '0.448', '0.5493', '0.1991', '0.595', '-0.01241', '0.1448', '-0.05353', '0.7363', '0.544', '0.2546', '0.03226', '0.1859', '-0.0875']",,0009036,,,,,
mondo:0014685,progressive myoclonic epilepsy type 9,"['PME type 9', 'epilepsy, progressive myoclonic, 9', 'progressive myoclonic epilepsy due to LMNB2 deficiency', 'EPM9', 'progressive myoclonic epilepsy caused by mutation in LMNB2', 'LMNB2 progressive myoclonic epilepsy', 'progressive myoclonus epilepsy type 9', 'epilepsy, progressive myoclonic, type 9']",0111450,616540,457265,C4225289,,,,,,,,
mondo:0014686,"short stature, microcephaly, and endocrine dysfunction","['short stature, microcephaly, and endocrine dysfunction', 'SSMED']",,616541,,C4225288,,,,,,,,
mondo:0014687,retinitis pigmentosa 73,"['HGSNAT retinitis pigmentosa', 'RP73', 'retinitis pigmentosa caused by mutation in HGSNAT', 'retinitis pigmentosa type 73', 'retinitis pigmentosa 73']",0110389,616544,,C4225287,,,,,,H35.5,,
mondo:0014688,short-rib thoracic dysplasia 14 with polydactyly,"['SRTD14', 'short-rib thoracic dysplasia 14 with polydactyly']",0110096,616546,,C4225286,,,,,,,,
mondo:0014689,Klippel-Feil anomaly-myopathy-facial dysmorphism syndrome,"['Klippel-Feil syndrome 4, autosomal recessive, with myopathy and facial dysmorphism', 'KFS4', 'Klippel-Feil syndrome 4, autosomal recessive, with nemaline myopathy and facial dysmorphism']",0080592,616549,447974,C4225285,,,,,,,,
mondo:0014690,"dyskeratosis congenita, autosomal dominant 6","['autosomal dominant dyskeratosis congenita 6', 'DKCA6', 'dyskeratosis congenita, autosomal recessive 7', 'dyskeratosis congenita, autosomal dominant type 6', 'dyskeratosis congenita, autosomal dominant 6']",0070023,616553,3322,C4225284,,C176924,,,,,,
mondo:0014691,Noonan syndrome 9,"['SOS2 Noonan syndrome', 'Noonan syndrome type 9', 'NS9', 'Noonan syndrome caused by mutation in SOS2', 'Noonan syndrome 9']",0060587,616559,,C4225282,,C176937,,,,,,
mondo:0014692,retinitis pigmentosa 74,"['retinitis pigmentosa caused by mutation in BBS2', 'retinitis pigmentosa 74', 'BBS2 retinitis pigmentosa', 'retinitis pigmentosa type 74', 'RP74']",0110401,616562,,C4225281,,,,,,H35.5,,
mondo:0014693,Noonan syndrome 10,"['LZTR1 Noonan syndrome', 'NS10', 'Noonan syndrome 10', 'Noonan syndrome type 10', 'Noonan syndrome caused by mutation in LZTR1']",0060588,616564,,C4225280,,C176938,,,,,,
mondo:0014694,"spondylocostal dysostosis 6, autosomal recessive","['autosomal recessive spondylocostal dysostosis caused by mutation in RIPPLY2', 'spondylocostal dysostosis 6', 'SCDO6', 'RIPPLY2 autosomal recessive spondylocostal dysostosis', 'spondylocostal dysostosis 6, autosomal recessive']",0112360,616566,,C4225279,,,,,,,,
mondo:0014695,glioma susceptibility 9,"['GLM9', 'malignant glioma caused by mutation in Pot1', 'POT1 malignant glioma', 'Pot1 malignant glioma', 'glioma susceptibility type 9', 'glioma susceptibility 9']",,616568,251630,,,,,,,,,
mondo:0014696,cerebrooculofacioskeletal syndrome 3,"['cerebrooculofacioskeletal syndrome type 3', 'COFS3', 'cerebrooculofacioskeletal syndrome 3']",0080913,616570,,C1851443,,,,C565035,,,,
mondo:0014697,"immunodeficiency, common variable, 12","['common variable immunodeficiency caused by mutation in NFKB1', 'NFKB1 deficiency', 'immunodeficiency, common variable, type 12', 'immunodeficiency, common variable, 12', 'NFKB1 common variable immunodeficiency', 'CVID12']",0081154,616576,,C4225277,,,,,,,,
mondo:0014698,microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome,"['EHLMRS', 'neurodevelopmental disorder with hearing loss, seizures, and brain abnormalities', 'microcephaly-intellectual disability-sensorineural deafness-epilepsy-abnormal muscle tone syndrome', 'epilepsy, hearing loss, and mental retardation syndrome', 'epilepsy, hearing loss, and intellectual disability syndrome']",,616577,457351,C4225276,,,,,,,,
mondo:0014699,"intellectual disability, autosomal dominant 40","['intellectual disability, autosomal dominant 40', 'intellectual disability, autosomal dominant type 40', 'MRD40', 'autosomal dominant non-syndromic intellectual disability caused by mutation in CHAMP1', 'mental retardation, autosomal dominant type 40', 'mental retardation, autosomal dominant 40', 'CHAMP1 autosomal dominant non-syndromic intellectual disability', 'autosomal dominant intellectual disability 40', 'autosomal dominant non-syndromic intellectual disability 40', 'autosomal dominant mental retardation 40']",0070070,616579,,C4225275,,,,,,,,
mondo:0014700,neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to a point mutation,"['AUKS', 'AU-Kline syndrome', 'Au-Kline syndrome']",,616580,453504,CN237748,"['-0.09', '0.0934', '0.05966', '-0.013306', '0.0702', '-0.1387', '0.002096', '0.1439', '-0.0933', '-0.1014', '0.006737', '6.115e-05', '0.004673', '0.0111', '-0.01286', '-0.05', '-0.01141', '-0.01163', '-0.05896', '-0.1924', '-0.000459', '-0.00564', '0.1119', '-0.05502', '0.04086', '-0.02342', '-0.01226', '-0.00983', '0.05978', '-0.04843', '0.0678', '0.00108', '0.1255', '0.0486', '0.01175', '-0.06824', '-0.0052', '-0.05814', '-0.0098', '-0.1267', '0.0547', '-0.1106', '0.02252', '-0.05905', '-0.03555', '-0.09485', '-0.0188', '0.04227', '0.0728', '0.04044', '-0.04144', '-0.0391', '0.005875', '0.0166', '-0.05923', '-0.04968', '0.1151', '-0.02599', '-0.1113', '0.02953', '0.0852', '0.0701', '0.02385', '0.01633', '0.01973', '0.0178', '0.1279', '0.05457', '-0.10315', '0.0922', '-0.1113', '-0.01048', '0.011024', '-0.0771', '0.05167', '0.06433', '0.03015', '0.001323', '-0.07495', '-0.01941', '-0.002693', '0.0367', '-0.03114', '0.11005', '-0.01881', '-0.01526', '0.04776', '0.1173', '0.1498', '0.0293', '0.02133', '0.074', '-0.01619', '0.005486', '0.204', '0.0523', '0.1178', '-0.1832', '0.01717', '0.0417']",,,,,,,
mondo:0014701,"spondyloepiphyseal dysplasia, Stanescu type","['spondyloepiphyseal dysplasia, Stanescu type', 'SEDSTN', 'SED, Stanescu type']",0112281,616583,459051,C4225273,"['0.0008483', '0.01563', '-0.00238', '-0.01616', '0.01982', '-0.009476', '0.008995', '0.007484', '-0.01686', '-0.00599', '-0.005413', '0.000944', '0.005695', '-0.00543', '0.005684', '-0.01039', '0.003986', '-0.01047', '-0.007626', '-0.02148', '0.003311', '-0.004425', '0.01851', '0.003513', '-0.0013485', '0.0086', '-0.00228', '-0.00764', '-0.002567', '-0.01455', '0.001438', '0.000902', '0.01633', '0.01095', '0.005253', '-0.003717', '0.0005813', '-0.00856', '0.009834', '-0.01068', '0.00834', '-0.02032', '0.007256', '0.001418', '0.00603', '-0.01231', '-0.00518', '0.02019', '0.003267', '-0.00226', '0.00542', '-0.00888', '-0.003386', '-0.001005', '-0.005753', '-0.01909', '0.01021', '-0.01491', '-0.01525', '0.007687', '0.002537', '0.01004', '-0.001323', '0.001631', '-0.006916', '-0.00837', '0.01762', '0.01371', '-0.006203', '0.01645', '-0.00649', '0.01131', '-0.001281', '-0.003714', '0.01304', '0.001339', '-0.00951', '0.00815', '-0.0165', '0.0006146', '-0.00802', '-0.007812', '-0.004345', '0.01921', '0.00456', '0.00957', '0.00609', '0.01395', '0.02142', '0.003738', '0.003271', '0.0043', '-0.0006204', '0.00861', '0.03375', '0.001952', '0.012955', '-0.0217', '0.007576', '0.0003252']",,,,,,,
mondo:0014702,autosomal recessive complex spastic paraplegia type 9B,"['hereditary spastic paraplegia type 9B', 'ALDH18A1 autosomal recessive complex spastic paraplegia', 'AR-SPG9B', 'autosomal recessive complex spastic paraplegia caused by mutation in ALDH18A1', 'autosomal recessive complex spastic paraplegia type 9B', 'spastic paraplegia 9B, autosomal recessive', 'autosomal recessive spastic paraplegia 9B', 'hereditary spastic paraplegia 9B', 'SPG9B']",0110825,616586,447760,C4225272,,,,,,,,
mondo:0014703,Adams-Oliver syndrome 6,"['Adams-Oliver syndrome caused by mutation in DLL4', 'AOS6', 'DLL4 Adams-Oliver syndrome', 'Adams-Oliver syndrome type 6', 'Adams-Oliver syndrome 6']",,616589,,C4225271,,,,,,,,
mondo:0014704,skeletal overgrowth-craniofacial dysmorphism-hyperelastic skin-white matter lesions syndrome,"['skeletal overgrowth with Facial Dysmorphism, hyperelastic skin, White matter lesions, and neurologic deterioration', 'KOGS', 'Kosaki overgrowth syndrome']",,616592,477831,C4225270,,,,,,,,
mondo:0014705,craniosynostosis 6,"['craniosynostosis 6', 'CRS6', 'craniosynostosis type 6', 'ZIC1 craniosynostosis', 'craniosynostosis caused by mutation in ZIC1']",,616602,,C4225269,,,,,,,,
mondo:0014706,"cutis laxa, autosomal dominant 3","['ADCL3', 'cutis laxa, autosomal dominant type 3', 'cutis laxa, autosomal dominant 3', 'autosomal dominant cutis laxa 3']",0070131,616603,,C4225268,,,,,,,,
mondo:0014707,14q32 duplication syndrome,"['trisomy 14q32', 'chromosome 14q32 DUPLICATION syndrome, 700-KB', 'predisposition to adult-onset myeloproliferative neoplasm due to 14q32 duplication', 'myeloproliferative neoplasms, familial, susceptibility to', 'dup(14)q(32)']",,616604,488280,C4225449,,,,,,,,
mondo:0014708,ring chromosome 14,"['chromosome 14 ring', 'Ring chromosome type 14', 'ring chromosome 14 syndrome, isolated cases', 'Ring 14', 'RING chromosome 14 syndrome']",,616606,1440,CN233170,,,,C535487,758.89,,,
mondo:0014710,autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency,"['autosomal recessive primary immunodeficiency due to RORC mutation', 'RORC autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency', 'IMD42', 'immunodeficiency type 42', 'autosomal recessive MSMD due to complete RORgamma receptor defiency', 'immunodeficiency 42']",0111940,616622,477857,C4225266,,,,,,,,
mondo:0014711,autosomal dominant Charcot-Marie-Tooth disease type 2W,"['Charcot-Marie-Tooth disease, axonal, type 2W', 'Charcot-Marie-Tooth disease, axonal type 2W', 'Charcot-Marie-Tooth disease type 2 caused by mutation in HARS', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2W', 'Charcot-Marie-Tooth neuropathy, type 2W', 'Charcot-Marie-Tooth disease, axonal, type 2w', 'HARS Charcot-Marie-Tooth disease type 2', 'CMT2W', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2W', 'Charcot-Marie-Tooth neuropathy type 2W', 'autosomal dominant Charcot-Marie-Tooth disease type 2 due to HARS mutation']",0110162,616625,488333,C4225265,,,,,,,,
mondo:0014712,Senior-Loken syndrome 9,"['Senior-Loken syndrome type 9', 'TRAF3IP1 Senior-Loken syndrome', 'Senior-Loken syndrome caused by mutation in TRAF3IP1', 'Senior-Loken syndrome 9', 'SLSN9']",,616629,,C4225263,,,,,,,,
mondo:0014713,"porokeratosis 9, multiple types","['FDPS porokeratosis (disease)', 'porokeratosis 9, multiple types', 'POROK9']",,616631,,C4225262,,,,,,,,
mondo:0014714,progressive microcephaly-seizures-cortical blindness-developmental delay syndrome,"['seizures, cortical blindness, microcephaly syndrome', 'seizures, cortical blindness, and microcephaly syndrome', 'SCBMS']",,616632,477814,C4225261,,,,,,,,
mondo:0014715,primary immunodeficiency with post-measles-mumps-rubella vaccine viral infection,"['primary immunodeficiency with post-MMR vaccine viral infection', 'immunodeficiency 44', 'IMD44', 'immunodeficiency type 44']",0111975,616636,431166,C4225260,,,,,,,,
mondo:0014716,macrocephaly-intellectual disability-neurodevelopmental disorder-small thorax syndrome,"['SKS', 'macrocephaly, seizures, mental retardation, umbilical hernia, and Facial Dysmorphism', 'MINDS syndrome', 'Smith-Kingsmore syndrome', 'macrocephaly, seizures, intellectual disability, umbilical hernia, and Facial Dysmorphism', 'SMITH-Kingsmore syndrome']",,616638,457485,C4225259,"['-0.1738', '0.1823', '0.421', '-0.4304', '0.0575', '-0.3179', '0.10425', '0.415', '-0.4683', '-0.1581', '0.04395', '-0.0904', '0.1252', '-0.1109', '-0.1421', '0.1724', '0.2979', '-0.0559', '-0.1573', '-0.4446', '0.05283', '0.18', '0.1677', '-0.1536', '0.2903', '-0.2332', '-0.175', '-0.11847', '0.2433', '-0.2817', '0.3916', '-0.3186', '0.681', '0.3066', '0.1868', '-0.05392', '-0.2952', '-0.1912', '-0.2988', '-0.4456', '0.2607', '-0.3176', '-0.1969', '-0.1458', '0.1016', '-0.1985', '0.1909', '0.515', '-0.2773', '0.04776', '-0.3286', '0.2064', '-0.234', '0.09045', '-0.02132', '-0.0245', '-0.09467', '-0.1399', '-0.1041', '0.218', '0.1963', '-0.0217', '-0.2747', '0.2477', '-0.0656', '-0.1411', '0.2168', '0.3813', '-0.1797', '0.3567', '-0.4263', '0.2367', '0.1868', '-0.05975', '-0.2673', '-0.003746', '0.3052', '-0.25', '-0.4429', '-0.0708', '0.1716', '0.1125', '-0.4053', '0.4712', '0.10547', '0.1045', '-0.1719', '0.3364', '0.255', '0.168', '0.0847', '0.3696', '0.3447', '0.2085', '0.592', '0.0446', '0.3005', '-0.10944', '0.4536', '0.374']",,0009050,,,,,
mondo:0014717,early-onset Lafora body disease,"['epilepsy, progressive myoclonic, 10', 'EPM10', 'epilepsy, progressive myoclonic, type 10']",0111445,616640,324290,C4518574,"['-0.4001', '0.3804', '-0.61', '-0.257', '-0.2493', '-0.8223', '0.1699', '0.1962', '-1.066', '-0.02466', '-0.582', '-0.0435', '0.105', '-0.257', '0.6313', '-0.1833', '0.2288', '-0.04193', '-0.425', '-0.62', '0.3875', '-0.4065', '-0.54', '-0.0371', '0.348', '-0.1293', '-0.1045', '-0.1472', '-0.5493', '0.3616', '0.4932', '0.245', '0.2313', '0.114', '0.3516', '0.1654', '-0.5103', '-0.2656', '-0.225', '-0.3296', '0.3367', '-0.6685', '0.2289', '-0.1405', '0.5083', '-0.289', '-0.428', '-0.01545', '0.04605', '0.5747', '-0.07745', '0.9673', '-0.6406', '-0.007576', '0.0393', '-0.215', '0.4875', '-0.4082', '-0.188', '-0.3376', '0.3535', '-0.1324', '0.494', '-0.2761', '-0.3484', '0.068', '0.744', '0.1802', '-0.2317', '0.6685', '-0.3325', '-0.2751', '0.4048', '-0.0269', '0.1575', '0.02783', '0.09546', '0.567', '0.05112', '-0.1686', '0.1519', '-0.4336', '-0.1543', '0.154', '0.4763', '0.1486', '-0.00418', '0.286', '0.563', '0.3105', '0.4116', '0.005466', '-0.08716', '0.1343', '-0.177', '0.564', '0.678', '-0.003761', '0.0937', '0.06995']",,,,,,,
mondo:0014718,"developmental and epileptic encephalopathy, 34","['epileptic encephalopathy, early infantile, 34', 'epileptic encephalopathy, early infantile, type 34', 'DEE34', 'EIEE34', 'developmental and epileptic encephalopathy 34', 'SLC12A5 early infantile epileptic encephalopathy', 'early infantile epileptic encephalopathy caused by mutation in SLC12A5']",0080460,616645,,C4225257,,,,,,,,
mondo:0014719,"developmental and epileptic encephalopathy, 35","['ITPA-related encephalopathy', 'epileptic encephalopathy, early infantile, 35', 'DEE35', 'developmental and epileptic encephalopathy 35', 'epileptic encephalopathy, early infantile, type 35', 'EIEE35']",0080458,616647,457375,C4225256,,,,,,,,
mondo:0014720,autosomal dominant optic atrophy plus syndrome,"['DOA+', 'optic atrophy type 8', 'optic atrophy-deafness-polyneuropathy-myopathy syndrome', 'dominant optic atrophy, deafness, ptosis, ophthalmoplegia, dystaxia, and myopathy', 'Treft-Sanborn-Carey syndrome', 'optic atrophy - deafness- polyneuropathy - myopathy']",0111340,,1215,C4275164,"['-0.01556', '0.1919', '-0.2869', '-0.04303', '0.1813', '-0.643', '0.11487', '0.675', '-0.272', '-0.9443', '-0.03897', '-0.6523', '-0.08124', '0.459', '-0.1917', '-0.7617', '-0.01091', '0.2075', '0.09766', '-0.4668', '-0.3923', '-0.9146', '-0.4636', '-0.4214', '-0.2883', '-0.1954', '-0.6533', '-0.1318', '-0.1866', '-0.3193', '0.3335', '0.02153', '0.3486', '-0.3162', '-0.1707', '-0.858', '-0.05762', '-0.6304', '-0.4436', '-0.1116', '-0.1763', '-0.2905', '0.371', '0.1484', '0.287', '-0.305', '-0.3784', '-0.3257', '-0.1957', '0.2185', '0.1247', '0.6475', '0.0152', '-0.1827', '1.21', '-0.5015', '0.7227', '-0.6426', '-0.4128', '0.1323', '0.1638', '0.0672', '0.6577', '0.6377', '-0.651', '0.525', '0.686', '0.7925', '0.2861', '1.05', '-0.198', '-0.1968', '0.4146', '0.05692', '0.907', '-0.1569', '0.2903', '0.115', '-0.11536', '-0.02905', '0.524', '0.1891', '0.3286', '1.044', '-0.1364', '0.1858', '0.00515', '-0.07825', '-0.02588', '0.2405', '0.734', '0.1531', '0.1301', '0.06494', '0.2278', '-0.149', '0.5303', '0.02475', '-0.2402', '-0.1465']",,,,,,,
mondo:0014722,Roifman syndrome,"['ROIFMAN syndrome', 'spondyloepiphyseal dysplasia-retinal dystrophy-immunodeficiency syndrome', 'RFMN', 'spondyloepiphyseal dysplasia, retinal dystrophy, and antibody deficiency', 'spondyloepiphseal dysplasia, retinal dystrophy and antibody deficiency', 'Roifman syndrome']",,616651,353298,C1846059,,,,C535866,,,,
mondo:0014723,PMP22-RAI1 contiguous gene duplication syndrome,"['YUAN-Harel-Lupski syndrome', 'Yuan-Harel-Lupski syndrome', 'trisomy 17p11.2p12', 'trisomy 17p11.2-p12', 'dup(17)(p11.2p12)', '17p11.2p12 microduplication syndrome', 'YUHAL']",,616652,477817,C4225255,,,,,,,,
mondo:0014724,Joubert syndrome 24,"['TCTN2 Joubert syndrome', 'JBTS24', 'Joubert syndrome 24', 'Joubert syndrome caused by mutation in TCTN2', 'Joubert syndrome type 24']",0110993,616654,,C4084841,,,,,,,,
mondo:0014725,spastic tetraplegia-thin corpus callosum-progressive postnatal microcephaly syndrome,"['spastic tetraplegia, thin corpus callosum, and progressive microcephaly', 'ASCT1 deficiency', 'spastic quadriplegia-thin corpus callosum-progressive postnatal microcephaly syndrome', 'SPATCCM']",,616657,447997,C4225254,"['-0.0758', '0.1455', '0.06152', '-0.11633', '0.02673', '-0.10535', '-0.01895', '0.1945', '-0.181', '-0.0753', '-0.05936', '-0.0341', '0.01625', '-0.03897', '0.000655', '-0.0999', '0.031', '-0.0143', '-0.01448', '-0.2141', '0.0659', '-0.04047', '0.03357', '-0.06726', '0.03546', '-0.00636', '-0.0216', '0.01345', '-0.01065', '-0.0932', '0.0665', '-0.035', '0.2014', '0.0376', '0.0009537', '-0.01515', '-0.051', '-0.0499', '-0.07556', '-0.03592', '0.0454', '-0.11646', '-0.00711', '-0.00646', '-0.006145', '-0.1631', '-0.006855', '0.05493', '0.001648', '-0.001737', '-0.0588', '-0.00254', '-0.0715', '-0.005577', '-0.0564', '-0.05194', '0.0603', '-0.06616', '-0.09937', '0.0708', '0.01787', '0.03632', '0.02866', '0.07745', '-0.03336', '0.012794', '0.10846', '0.10065', '-0.1431', '0.1156', '-0.1317', '0.10596', '0.0764', '-0.0788', '0.03336', '0.00534', '0.0419', '-0.0641', '-0.0725', '-0.0649', '-0.01947', '0.0645', '-0.08765', '0.132', '-0.02982', '0.00765', '0.02655', '0.1283', '0.12115', '0.02893', '0.02773', '0.158', '0.02202', '0.04776', '0.1919', '0.03577', '0.13', '-0.1128', '0.10443', '0.0819']",,,,,,,
mondo:0014726,Charcot-Marie-Tooth disease axonal type 2X,"['autosomal recessive Charcot Marie Tooth disease type 2X', 'Charcot-Marie-Tooth neuropathy, type 2X', 'autosomal recessive Charcot-Marie-Tooth disease type 2X', 'Charcot-Marie-Tooth neuropathy type 2X', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2X', 'ARCMT2X', 'Charcot-Marie-Tooth disease caused by mutation in SPG11', 'autosomal recessive axonal Charcot-Marie-Tooth disease type 2X', 'CMT2X', 'Charcot-Marie-Tooth disease, axonal, type 2x', 'autosomal recessive Charcot-Marie-Tooth disease type 2 due to SPG11 mutation', 'SPG11 Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth disease, axonal, type 2X']",0110176,616668,466775,C4225253,"['0.261', '0.11884', '0.0962', '0.0555', '0.05963', '-0.4036', '-0.007416', '0.7354', '-0.8516', '-0.2203', '0.076', '0.445', '-0.5435', '0.733', '-0.1595', '-0.08105', '-0.1888', '-0.647', '-0.7065', '-0.3667', '0.01976', '0.2407', '0.1356', '0.782', '0.2308', '0.4172', '-0.05527', '0.10657', '0.1815', '-0.1021', '0.2129', '-0.797', '0.06055', '0.1912', '0.5073', '-0.6367', '-0.3792', '-0.3154', '0.4905', '0.1309', '-1.169', '-0.3362', '-0.5947', '0.645', '-0.2532', '-0.2219', '0.1333', '-0.08905', '-0.26', '0.00893', '0.01765', '0.39', '-0.2646', '-0.7876', '0.2646', '-0.1448', '0.119', '0.1317', '-0.6924', '-0.2957', '-0.1375', '0.1936', '0.5693', '0.3125', '-0.646', '1.088', '-0.07404', '0.5957', '-0.4192', '0.2969', '-0.886', '0.2119', '0.1565', '-0.2175', '0.929', '0.508', '-0.2896', '0.2922', '0.07214', '-0.7124', '-0.1672', '0.01764', '0.752', '0.4658', '0.0189', '-0.1533', '0.2428', '0.4272', '0.7236', '0.4634', '0.05295', '0.0327', '0.05972', '0.2725', '0.4531', '0.603', '0.727', '-0.5767', '0.0684', '0.5977']",,1001983,,,,,
mondo:0014727,immunodeficiency 45,"['immunodeficiency type 45', 'immunodeficiency 45', 'IMD45']",0111994,616669,,C4225252,,,,,,,,
mondo:0014728,combined oxidative phosphorylation defect type 27,"['combined oxidative phosphorylation deficiency type 27', 'CARS2 combined oxidative phosphorylation deficiency', 'COXPD27', 'combined oxidative phosphorylation deficiency 27', 'combined oxidative phosphorylation deficiency caused by mutation in CARS2']",0111489,616672,477774,C4225251,"['-0.4517', '0.0658', '0.0721', '-0.04688', '-0.0496', '-0.5107', '0.1682', '0.3115', '-0.595', '-0.04123', '-0.3896', '-0.4377', '-0.1903', '-0.346', '0.3977', '-0.4458', '0.0979', '-0.256', '-0.3945', '-0.643', '0.2822', '-0.2832', '0.1194', '0.0118', '0.1844', '-0.08887', '0.07227', '0.1', '-0.37', '-0.0295', '0.0652', '0.4226', '0.543', '0.1815', '0.1656', '-0.0535', '-0.1836', '-0.165', '0.0232', '-0.1582', '0.309', '-0.4897', '0.0932', '0.3035', '-0.3657', '-0.5527', '-0.004772', '-0.05878', '-0.1671', '0.06445', '-0.04407', '0.385', '-0.0793', '-0.1334', '-0.08386', '-0.0964', '0.2185', '-0.1594', '0.003668', '0.277', '-0.05463', '0.0697', '0.4958', '-0.2031', '-0.2408', '0.2245', '0.3887', '0.4658', '-0.3435', '0.2395', '-0.0576', '0.3328', '-0.1357', '-0.04663', '0.08923', '-0.1525', '0.3164', '-0.1509', '0.06805', '0.2487', '-0.03363', '0.03726', '-0.1257', '0.4822', '0.03088', '-0.1691', '0.2446', '0.4102', '0.521', '0.2556', '0.4814', '0.2878', '0.0395', '-0.01749', '0.539', '0.4387', '0.397', '-0.048', '0.4736', '0.06396']",,0009037,,,,,
mondo:0014729,hereditary spastic paraplegia 75,"['autosomal recessive spastic paraplegia 75', 'autosomal recessive spastic paraplegia type 75', 'hereditary spastic paraplegia type 75', 'hereditary spastic paraplegia caused by mutation in MAG', 'spastic paraplegia 75, autosomal recessive', 'MAG hereditary spastic paraplegia', 'SPG75']",0110820,616680,459056,C4225250,"['-0.1648', '0.1423', '-0.1598', '-0.386', '-0.268', '-0.7524', '-0.294', '0.06604', '-0.518', '-0.5537', '0.00578', '-0.05862', '-0.2625', '0.221', '0.5327', '-0.04898', '-0.24', '-0.1765', '0.321', '-0.2585', '0.2451', '-0.1606', '0.0161', '0.3123', '0.3062', '0.0974', '0.2283', '-0.01033', '-0.1567', '-0.01701', '0.2874', '0.2014', '0.123', '0.3552', '0.07837', '-0.5264', '-0.3293', '-0.4832', '-0.2852', '-0.3435', '0.2415', '-0.538', '0.02768', '0.2441', '-0.1827', '-0.4258', '-0.1509', '0.2065', '0.06647', '-0.1121', '0.1663', '0.3044', '-0.4658', '-0.4878', '0.1302', '-0.6304', '0.8145', '-0.1046', '-0.4182', '0.3557', '-0.208', '-0.1351', '0.2542', '0.3638', '-0.534', '0.1895', '0.1785', '0.9316', '0.02994', '0.511', '-0.486', '0.063', '0.0173', '-0.6587', '1.009', '0.336', '0.03384', '-1.127e-05', '-0.0981', '-0.0111', '0.0745', '-0.3647', '0.4138', '1.084', '-0.0403', '-0.1483', '0.01366', '0.2556', '0.0698', '0.1248', '0.6494', '0.05493', '-0.04675', '0.2297', '0.978', '0.4504', '0.5044', '0.0232', '0.2039', '0.01499']",,0009018,,,,,
mondo:0014730,"microcephaly 16, primary, autosomal recessive","['microcephaly 16, primary, autosomal recessive', 'MCPH16']",0070289,616681,,C4225249,,,,,,,,
mondo:0014731,seizures-scoliosis-macrocephaly syndrome,"['SSM syndrome', 'seizures, scoliosis, and macrocephaly syndrome', 'SSMS']",,616682,466926,C4225248,"['-0.0083', '0.007404', '-0.0008807', '0.0003', '-0.00832', '0.002573', '-0.001082', '-0.002726', '-0.00929', '-0.01073', '-0.00376', '-0.0096', '0.00812', '0.007576', '-0.005005', '0.004417', '0.004044', '0.001736', '0.004528', '-0.005478', '0.006817', '-0.005', '0.000525', '-0.001187', '0.001171', '0.001789', '-0.00629', '-0.001348', '0.005146', '0.005234', '0.0009694', '-0.0014105', '0.0129', '0.004734', '-0.00537', '0.001875', '-0.001605', '-0.003216', '-0.0009313', '-0.004154', '-0.007412', '-0.011765', '-0.005856', '-0.003075', '0.00885', '-0.002335', '0.002071', '0.00965', '0.0003889', '-0.00471', '-0.01018', '0.006104', '0.003202', '-0.00825', '0.004566', '0.003937', '0.01164', '-0.00964', '-0.014626', '0.00346', '0.0002409', '0.010155', '0.00010145', '-0.006584', '0.004063', '0.007267', '0.00918', '0.003466', '-0.007404', '0.01406', '-0.00823', '-0.0002167', '-0.00792', '-0.011086', '0.00168', '0.01281', '0.003502', '-0.000534', '0.0003452', '0.003216', '0.005516', '-0.007595', '-0.004597', '0.01288', '-0.006374', '0.00653', '0.011765', '0.01488', '-0.001136', '-0.00528', '0.00942', '0.00678', '0.003014', '-0.0036', '0.00828', '0.01074', '-0.0008516', '-0.01461', '0.003052', '0.006664']",,,,,,,
mondo:0014732,hypomyelinating leukodystrophy 12,"['VPS11-related autosomal recessive hypomyelinating leukodystrophy', 'leukodystrophy, hypomyelinating, 12', 'hypomyelinating leukodystrophy type 12', 'leukodystrophy caused by mutation in VPS11', 'VPS11 leukodystrophy', 'leukodystrophy, hypomyelinating, type 12', 'VPS11-related autosomal recessive hypomyelinating leukoencephalopathy', 'HLD12']",0060796,616683,466934,C4225247,"['-0.02557', '0.04248', '0.004604', '-0.00256', '-0.003479', '-0.05106', '-0.007343', '0.0454', '-0.04034', '-0.00808', '-0.03137', '-0.01746', '0.003239', '0.005936', '0.003736', '-0.02605', '0.00916', '-0.02171', '-0.006065', '-0.06152', '-0.0075', '-0.01482', '0.03104', '-0.02464', '0.02777', '-0.02838', '-0.00557', '-0.00887', '-0.0008187', '-0.01672', '0.02536', '0.01668', '0.03592', '0.005238', '0.01442', '-0.009155', '-0.021', '-0.01421', '-0.0176', '-0.04413', '0.02428', '-0.0663', '0.01315', '-0.02235', '0.006855', '-0.0345', '0.0007286', '0.03568', '0.01014', '0.00501', '0.00888', '-0.0003147', '-0.03058', '-0.01735', '-0.0171', '-0.01051', '0.04553', '-0.0195', '-0.05884', '0.02399', '0.01915', '0.011375', '0.02365', '0.01631', '-0.01128', '-0.012405', '0.05002', '0.0326', '-0.04218', '0.04437', '-0.0374', '0.01294', '0.02162', '-0.02786', '0.01383', '0.01813', '0.012665', '-0.00822', '-0.0287', '-0.03317', '-0.00528', '-0.01761', '-0.01651', '0.02809', '-0.004005', '-0.005802', '0.011856', '0.03613', '0.05237', '0.007904', '0.01181', '0.04056', '-0.004147', '0.01834', '0.08704', '0.01006', '0.04654', '-0.064', '-0.003435', '0.01804']",,,,,,,
mondo:0014733,Charcot-Marie-Tooth disease type 4K,"['SURF1 Charcot-Marie-Tooth disease type 4', 'CMT4K', 'SURF1-related severe demyelinating Charcot-Marie-Tooth disease', 'autosomal recessive demyelinating Charcot-Marie-Tooth neuropathy type 4K', 'SURF1-related Charcot-Marie-Tooth disease type 4', 'Charcot-Marie-Tooth neuropathy, demyelinating, autosomal recessive, type 4K', 'Charcot-Marie-Tooth disease type 4K', 'Charcot-Marie-Tooth disease, type 4K', 'SURF1-related CMT4', 'Charcot-Marie-Tooth disease type 4 caused by mutation in SURF1', 'Charcot-Marie-Tooth disease, type 4k', 'autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4K', 'Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4K']",0110187,616684,391351,C4225246,"['-0.0846', '0.1432', '-0.2424', '0.2568', '0.152', '-0.2878', '-0.07837', '1.1455', '-0.9297', '0.1906', '-0.1997', '0.01026', '-0.806', '0.04968', '-0.292', '-0.7446', '-0.1683', '-0.9614', '-0.6016', '-0.549', '-0.01242', '0.2446', '-0.1299', '0.402', '0.428', '0.365', '0.0603', '0.3765', '0.0831', '-0.0822', '-0.05792', '-0.1691', '0.129', '0.0971', '0.4512', '-0.595', '-0.4907', '-0.4648', '-0.01761', '0.1334', '-1.485', '-0.3267', '-0.5835', '0.4895', '-0.429', '-0.3967', '-0.0558', '0.18', '-0.1775', '-0.2144', '-0.06274', '-0.1853', '-0.671', '-1.318', '0.497', '0.04144', '-0.1163', '0.1798', '-0.7124', '0.007065', '-0.3452', '0.4333', '0.74', '0.7134', '-0.9863', '1.123', '-0.1802', '0.9775', '-0.3125', '0.3562', '-0.4321', '0.4307', '0.324', '-0.3818', '0.974', '0.2312', '-0.2122', '-0.04404', '0.01066', '-0.2484', '-0.1711', '-0.3633', '0.91', '0.633', '0.03833', '-0.0541', '0.425', '0.7246', '0.9526', '0.3416', '0.4958', '-0.01628', '-0.09717', '0.0938', '0.4233', '0.604', '0.6294', '-0.01463', '-0.0868', '0.7617']",,,,,,,
mondo:0014734,"epilepsy, idiopathic generalized, susceptibility to, 14","['susceptibility to idiopathic generalised epilepsy 14', 'EIG14', 'susceptibility to idiopathic generalized epilepsy 14', 'epilepsy, idiopathic generalized, susceptibility to, type 14', 'epilepsy, idiopathic generalized, susceptibility to, 14']",0111315,616685,,,,,,,,,,
mondo:0014735,Charcot-Marie-Tooth disease type 2Y,"['Charcot-Marie-Tooth disease type 2 caused by mutation in VCP', 'Charcot-Marie-Tooth neuropathy type 2Y', 'Charcot-Marie-Tooth disease, axonal, type 2Y', 'Charcot-Marie-Tooth disease, type 2Y', 'CMT2 due to VCP mutation', 'CMT2Y', 'Charcot-Marie-Tooth neuropathy, type 2Y', 'autosomal dominant Charcot-Marie-Tooth disease type 2Y', 'Charcot-Marie-Tooth disease, axonal, type 2y', 'autosomal dominant Charcot-Marie-Tooth disease type 2 due to VCP mutation', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2Y', 'VCP Charcot-Marie-Tooth disease type 2', 'autosomal dominant axonal Charcot-Marie-Tooth type 2Y']",0110168,616687,435387,C4225244,,C168974,,,,,,
mondo:0014736,Charcot-Marie-Tooth disease axonal type 2Z,"['MORC2 Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth neuropathy type 2Z', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2Z', 'Charcot-Marie-Tooth disease, axonal, type 2Z', 'Charcot-Marie-Tooth disease caused by mutation in MORC2', 'autosomal dominant Charcot-Marie-Tooth disease type 2 due to MORC2 mutation', 'CMT2Z', 'Charcot-Marie-Tooth neuropathy, type 2Z', 'autosomal dominant Charcot-Marie-Tooth disease type 2Z', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2Z', 'Charcot-Marie-Tooth disease, axonal, type 2z']",0110181,616688,466768,C4225243,,,,,,,,
mondo:0014737,dehydrated hereditary stomatocytosis 2,"['Desiccytosis Gardos', 'Dehydrated hereditary stomatocytosis 2', 'xerocytosis Gardos', 'dehydrated hereditary stomatocytosis caused by mutation in KCNN4', 'DHS2', 'KCNN4 dehydrated hereditary stomatocytosis', 'Dehydrated hereditary stomatocytosis type 2']",0111577,616689,,C4225242,,,,,,,,
mondo:0014738,autosomal dominant nonsyndromic hearing loss 69,"['DFNA69', 'deafness, autosomal dominant 69, unilateral or asymmetric', 'KITLG autosomal dominant nonsyndromic deafness', 'DCUA', 'autosomal dominant nonsyndromic deafness type 69', 'autosomal dominant nonsyndromic deafness 69', 'autosomal dominant deafness 69', 'autosomal dominant nonsyndromic deafness caused by mutation in KITLG', 'unilateral or asymmetric congenital deafness', 'deafness, congenital, unilateral or asymmetric', 'deafness, autosomal dominant 69']",0110590,616697,,C4225241,,,,,,,,
mondo:0014739,autosomal recessive nonsyndromic hearing loss 97,"['autosomal recessive nonsyndromic deafness caused by mutation in MET', 'DFNB97', 'autosomal recessive deafness 97', 'deafness, autosomal recessive type 97', 'autosomal recessive nonsyndromic deafness type 97', 'autosomal recessive nonsyndromic deafness 97', 'deafness, autosomal recessive 97', 'MET autosomal recessive nonsyndromic deafness']",0110539,616705,,C4084709,,,,,,,,
mondo:0014740,autosomal dominant nonsyndromic hearing loss 68,"['autosomal dominant deafness 68', 'autosomal dominant nonsyndromic deafness 68', 'deafness, autosomal dominant 68', 'deafness, autosomal dominant type 68', 'HOMER2 autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness type 68', 'DFNA68', 'autosomal dominant nonsyndromic deafness caused by mutation in HOMER2']",0110589,616707,,C4225240,,,,,,,,
mondo:0014741,DeSanto-Shinawi syndrome due to WAC point mutation,"['chromosome 10P12-p11 deletion syndrome', 'DESANTO-SHINAWI syndrome', 'DESSH', 'developmental delay, behavioral abnormalities, Facial Dysmorphism, and ocular abnormalities', 'facial dysmorphism-developmental delay-behavioral abnormalities syndrome due to WAC point mutation', 'Desanto-Shinawi syndrome', 'developmental delay, behavioural abnormalities, Facial Dysmorphism, and ocular abnormalities']",,616708,466950,CN242167,"['-0.02199', '0.02751', '0.007095', '-0.004276', '0.00926', '-0.02069', '-0.00242', '0.02565', '-0.02379', '-0.01605', '-0.003248', '0.003672', '0.006073', '0.01562', '-0.003298', '-0.004658', '-0.004402', '-0.00894', '-0.01032', '-0.04044', '-0.008385', '-0.004066', '0.03323', '-0.01084', '0.00782', '-0.003387', '-0.007305', '0.006752', '0.01118', '-0.00842', '0.02983', '0.003998', '0.02713', '0.01301', '0.00796', '-0.01048', '0.002953', '-0.01634', '-0.01053', '-0.02138', '0.0183', '-0.02663', '0.0071', '-0.01425', '-0.002153', '-0.01255', '-0.01068', '0.01037', '0.00537', '0.0007467', '-0.006718', '-0.00811', '0.000977', '-0.00505', '-0.01817', '-0.005978', '0.02904', '0.0005956', '-0.02818', '0.003918', '0.02034', '0.00414', '-0.00573', '0.00524', '-0.006424', '-0.002878', '0.02982', '0.03023', '-0.0278', '0.01901', '-0.03568', '-0.00554', '0.0004766', '-0.02351', '0.007656', '0.01588', '0.01428', '-0.000765', '-0.011314', '-0.01408', '-0.002981', '-0.00187', '-0.00875', '0.03078', '-0.008286', '-0.0008597', '0.00787', '0.02625', '0.02986', '0.01298', '0.01405', '0.02411', '-0.01458', '5e-05', '0.05353', '0.01697', '0.01323', '-0.03183', '0.0006375', '0.011665']",,,,,,,
mondo:0014742,"Parkinson disease 22, autosomal dominant","['CHCHD2 Parkinson disease', 'PARK22', 'Parkinson disease caused by mutation in CHCHD2', 'Parkinson disease 22, autosomal dominant']",0080504,616710,,C4225238,,,,,,,,
mondo:0014743,rhizomelic chondrodysplasia punctata type 5,"['RCDP5', 'Rcdp5', 'rhizomelic chondrodysplasia punctata type 5', 'rhizomelic chondrodysplasia punctata, type 5', 'rhizomelic chondrodysplasia punctata caused by mutation in PEX5', 'PEX5 rhizomelic chondrodysplasia punctata']",0110854,616716,468717,C4225237,,,,,,,,
mondo:0014744,acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome,"['autosomal recessive spinocerebellar ataxia 21', 'autosomal recessive spinocerebellar ataxia 21 with hepatopathy', 'spinocerebellar ataxia, autosomal recessive 21', 'acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome', 'autosomal recessive spinocerebellar ataxia type 21', 'SCAR21', 'spinocerebellar ataxia, autosomal recessive 21, with hepatopathy', 'spinocerebellar ataxia, autosomal recessive type 21']",0111155,616719,466794,C4225236,,,,,,,,
mondo:0014745,congenital myasthenic syndrome 19,"['congenital myasthenic syndrome type 19', 'CMS19', 'COL13A1 congenital myasthenic syndrome', 'myasthenic syndrome, congenital, 19', 'congenital myasthenic syndrome caused by mutation in COL13A1', 'myasthenic syndrome, congenital, type 19']",0110673,616720,,C4225235,,,,,,,,
mondo:0014746,SLC39A8-CDG,"['congenital disorder of glycosylation, type IIn', 'congenital disorder of glycosylation type 2n', 'CDG-IIn', 'carbohydrate deficient glycoprotein syndrome type IIn', 'CDG IIn', 'congenital disorder of glycosylation type IIn', 'CDG2N', 'CDG syndrome type IIn', 'SLC39A8 deficiency']",0070266,616721,468699,CN234734,"['-0.00632', '0.00952', '-0.009094', '-0.01137', '-0.006454', '-0.011734', '-0.002928', '0.01006', '-0.011154', '0.004883', '-0.00295', '-0.006767', '-0.00805', '0.008705', '-0.00878', '0.001494', '0.001416', '-0.01334', '-0.004234', '-0.008514', '-0.01048', '0.00263', '0.001042', '-0.001461', '0.006187', '-0.004616', '-0.01009', '-0.00486', '-0.001756', '-0.008995', '0.01007', '-0.00355', '0.01368', '0.010574', '-0.005554', '-0.003042', '-0.01133', '-0.007706', '-0.01023', '0.0002854', '0.00954', '0.005283', '0.001823', '0.007404', '-0.00894', '-0.001328', '-0.01118', '0.012955', '-0.001987', '0.004078', '0.0002245', '0.00391', '-0.003513', '0.006813', '-0.0094', '-0.01307', '0.00883', '0.007698', '0.001117', '0.004585', '0.00934', '-0.000126', '0.01023', '-0.00978', '0.0017185', '-0.00488', '0.00906', '0.01997', '-0.01386', '0.003075', '-0.01344', '0.007866', '-0.00389', '-0.00672', '0.01002', '6.646e-05', '0.003544', '0.001327', '0.00587', '-0.006924', '-0.01171', '0.0099', '0.003557', '-0.00268', '0.00922', '0.001241', '-0.002062', '0.01677', '0.01303', '-0.003223', '0.005676', '-0.002901', '0.006687', '0.005314', '0.013725', '0.01071', '-0.001474', '-0.00321', '-0.006298', '0.012566']",,,,,,,
mondo:0014747,familial progressive retinal dystrophy-iris coloboma-congenital cataract syndrome,"['retinal dystrophy and iris coloboma with or without congenital cataract', 'RDICC', 'retinal dystrophy and iris coloboma with or without cataract']",,616722,488197,C4225233,,,,,,,,
mondo:0014748,progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome,"['spondyloepimetaphyseal dysplasia, faden-Alkuraya type', 'spondyloepimetaphyseal dysplasia, faden-ALKURAYA type', 'SEMDFA', 'spondyloepimetaphyseal dysplasia, progressive, with short stature, Facial Dysmorphism, short fourth metatarsals, and mental retardation, with or without craniosynostosis', 'spondyloepimetaphyseal dysplasia, progressive, with short stature, Facial Dysmorphism, short fourth metatarsals, and intellectual disability, with or without craniosynostosis']",,616723,457395,C4225232,,,,,,,,
mondo:0014749,"tooth agenesis, selective, 7","['tooth agenesis, selective, type 7', 'tooth agenesis caused by mutation in LRP6', 'LRP6 tooth agenesis', 'tooth agenesis, selective, 7', 'STHAG7']",,616724,,C4225231,,,,,,,,
mondo:0014750,primary ciliary dyskinesia 33,"['ciliary dyskinesia, primary, 33', 'primary ciliary dyskinesia caused by mutation in GAS8', 'ciliary dyskinesia, primary, 33, without situs inversus', 'CILD33', 'GAS8 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, type 33', 'primary ciliary dyskinesia 33 without situs inversus', 'primary ciliary dyskinesia type 33']",0110619,616726,,C4225230,,,,,,,,
mondo:0014751,palatal anomalies-widely spaced teeth-facial dysmorphism-developmental delay syndrome,"['palatal anomalies-multiple diastemata-facial dysmorphism-developmental delay syndrome', 'CPRF', 'cleft palate, psychomotor retardation, and distinctive FACIAL features', 'cleft palate, psychomotor retardation, and distinctive Facial features']",,616728,477993,C4225229,,,,,,,,
mondo:0014752,"nephrotic syndrome, type 11","['NPHS11', 'NUP107 familial nephrotic syndrome', 'nephrotic syndrome, type 11', 'Nup107 familial nephrotic syndrome', 'familial nephrotic syndrome caused by mutation in Nup107']",0080385,616730,,C4225228,,,,,,,,
mondo:0014753,autosomal recessive optic atrophy,"['autosomal recessive nonsyndromic optic atrophy', 'autosomal recessive isolated optic atrophy']",,,98676,CN229293,"['-0.264', '-0.1198', '-0.1003', '-0.2612', '-0.2761', '0.02037', '0.2688', '-0.009125', '-0.1895', '-0.09393', '0.07715', '-0.2559', '-0.3499', '0.04318', '-0.01311', '-0.3853', '-0.02036', '-0.1151', '0.0778', '-0.534', '-0.089', '-0.2295', '-0.2162', '0.2705', '0.1849', '0.1826', '-0.1882', '0.098', '-0.3228', '-0.0293', '0.2002', '0.1455', '0.5176', '0.3767', '-0.1536', '-0.0807', '-0.1981', '-0.3037', '0.02722', '-0.2012', '0.006523', '-0.207', '0.008995', '0.0506', '0.1884', '-0.2185', '0.13', '-0.0983', '-0.01682', '-0.04208', '0.3022', '0.362', '0.1222', '-0.2275', '0.1873', '-0.1131', '0.605', '0.0727', '-0.5366', '0.01383', '0.05078', '-0.04428', '0.1615', '0.3425', '-0.5537', '0.1805', '0.4016', '0.8403', '-0.003637', '0.641', '-0.4531', '0.1118', '0.0748', '-0.2062', '0.1685', '-0.1552', '0.2563', '0.3953', '0.02405', '-0.2654', '0.08453', '-0.02469', '0.233', '0.8276', '-0.0965', '-0.1552', '0.2898', '0.03412', '0.2329', '0.06165', '0.3638', '0.2219', '0.04385', '0.0512', '0.6226', '0.1816', '0.268', '0.12274', '0.1709', '0.3447']",,,,,,,
mondo:0014754,primary coenzyme Q10 deficiency 8,"['COQ7 coenzyme Q10 deficiency', 'primary coenzyme Q10 deficiency 8', 'coenzyme Q10 deficiency, primary, type 8', 'coenzyme Q10 deficiency, primary, 8', 'coenzyme Q10 deficiency caused by mutation in COQ7', 'COQ10D8']",0070245,616733,,C4225226,,,,,,,,
mondo:0014755,"skin creases, congenital symmetric circumferential, 2","['skin creases, congenital symmetric circumferential, type 2', 'symmetric circumferential skin creases, congenital, 2', 'MAPRE2 multiple benign circumferential skin creases on limbs', 'CSCSC2', 'multiple benign circumferential skin creases on limbs caused by mutation in MAPRE2', 'skin creases, congenital symmetric circumferential, 2']",0112243,616734,,,,,,,,,,
mondo:0014756,"tremor, hereditary essential, 5","['tremor, hereditary essential, 5', 'tremor, hereditary essential, type 5', 'ETM5', 'essential tremor caused by mutation in TENM4', 'essential tremor, hereditary, 5', 'TENM4 essential tremor']",0111432,616736,,C4225223,,,,,,,,
mondo:0014757,macrothrombocytopenia-lymphedema-developmental delay-facial dysmorphism-camptodactyly syndrome,"['TAKENOUCHI-Kosaki syndrome', 'TKS', 'Takenouchi-Kosaki syndrome', 'macrothrombocytopenia and mental retardation syndrome', 'macrothrombocytopenia and intellectual disability syndrome']",,616737,487796,C4225222,"['-0.01131', '0.01877', '0.006218', '-0.0182', '0.002533', '-0.01707', '0.012184', '0.03235', '-0.01572', '-0.0097', '-0.0069', '-0.01126', '-0.00429', '0.01405', '0.001667', '-0.01593', '-0.011536', '0.006527', '-0.015015', '-0.03476', '0.0001762', '-0.004578', '0.01613', '-0.00613', '0.009026', '-0.00896', '-0.009056', '-0.00801', '0.002281', '-0.025', '0.0124', '-0.0069', '0.02478', '0.02188', '0.013535', '-0.01103', '-0.00849', '-0.01109', '-0.00427', '-0.01907', '0.003195', '-0.00949', '-0.004833', '-0.005516', '0.00548', '-0.03348', '-0.003714', '0.01548', '0.01229', '0.01238', '-0.001248', '-0.01377', '0.00526', '0.01294', '-0.009125', '-0.000775', '0.01947', '0.004234', '-0.02255', '0.001319', '0.00876', '0.0094', '0.002619', '0.005787', '-0.00982', '-0.01016', '0.01642', '0.00785', '-0.022', '0.03326', '-0.03366', '0.003763', '-0.002174', '-0.01968', '0.009056', '0.01195', '0.007053', '-0.008835', '-0.00985', '-0.004513', '0.007835', '0.01202', '-0.02208', '0.03003', '0.003597', '0.00751', '-0.001078', '0.0364', '0.0351', '-0.00218', '0.01052', '0.02628', '0.00821', '0.01473', '0.04404', '0.0145', '0.0151', '-0.03284', '-0.003593', '0.001014']",,,,,,,
mondo:0014758,radioulnar synostosis with amegakaryocytic thrombocytopenia 2,"['radioulnar synostosis with amegakaryocytic thrombocytopenia type 2', 'RUSAT2', 'radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome caused by mutation in MECOM', 'MECOM radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome', 'radioulnar synostosis with amegakaryocytic thrombocytopenia 2']",,616738,,C4225221,,,,,,,,
mondo:0014759,"intellectual disability, autosomal recessive 51","['intellectual disability, autosomal recessive 51', 'HNMT autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive 51', 'mental retardation, autosomal recessive type 51', 'intellectual developmental disorder, autosomal recessive 51', 'MRT51', 'autosomal recessive non-syndromic intellectual disability caused by mutation in HNMT', 'intellectual disability, autosomal recessive type 51']",0081214,616739,,C4225220,,,,,,,,
mondo:0014760,TFRC-related combined immunodeficiency,"['CID due to TFRC deficiency', 'immunodeficiency type 46', 'combined immunodeficiency due to TFRC deficiency', 'IMD46', 'immunodeficiency 46']",0111948,616740,476113,C4225219,,,,,,,,
mondo:0014762,"heterotaxy, visceral, 7, autosomal","['visceral heterotaxy caused by mutation in MMP21', 'HTX7', 'heterotaxy, visceral, 7, autosomal', 'MMP21 visceral heterotaxy']",,616749,,C4225217,,,,,,,,
mondo:0014764,spastic paraplegia-severe developmental delay-epilepsy syndrome,"['SPPRS', 'spastic paraplegia-psychomotor retardation-seizures syndrome', 'SPPRS syndrome', 'spastic paraplegia and psychomotor retardation with or without seizures']",,616756,464282,C4225215,"['-0.02711', '0.10077', '0.0252', '-0.03775', '0.01098', '-0.10754', '-0.0313', '0.11163', '-0.1042', '-0.04834', '-0.03662', '-0.01692', '0.01518', '-0.003952', '0.01727', '-0.07086', '0.01017', '-0.00784', '0.010765', '-0.1761', '0.01187', '-0.03574', '0.0359', '-0.03653', '0.0494', '-0.02527', '-0.01965', '0.01816', '0.015526', '-0.044', '0.0556', '-0.02617', '0.116', '0.035', '-0.007256', '-0.0205', '-0.02554', '-0.04388', '-0.0435', '-0.07135', '0.02345', '-0.0876', '-0.001155', '-0.009865', '0.00618', '-0.0771', '-0.04712', '0.06055', '0.03087', '0.008026', '-0.0679', '0.02214', '-0.02223', '-0.003595', '-0.01987', '-0.045', '0.05695', '-0.00997', '-0.0767', '0.04407', '0.04303', '0.0264', '0.0705', '0.02467', '-0.02025', '0.02347', '0.08496', '0.08344', '-0.1108', '0.09796', '-0.08936', '0.0416', '0.02719', '-0.063', '0.05603', '0.04605', '0.03613', '0.005238', '-0.03177', '-0.03595', '-0.01019', '0.01246', '-0.04074', '0.1116', '0.00108', '-0.0014715', '-0.00858', '0.07635', '0.1071', '0.0279', '0.0564', '0.10785', '0.013565', '0.01822', '0.1346', '0.0354', '0.0733', '-0.0912', '0.0207', '0.06137']",,,,,,,
mondo:0014765,"wooly hair, autosomal recessive 3","['ARWH3', 'KRT25 wooly hair (disease)', 'woolly hair, autosomal recessive type 3', 'woolly hair (disease) caused by mutation in KRT25', 'woolly hair, autosomal recessive 3, with hypotrichosis', 'KRT25 woolly hair (disease)', 'wooly hair, autosomal recessive type 3', 'wooly hair, autosomal recessive 3', 'wooly hair, autosomal recessive 3, with hypotrichosis']",0111574,616760,,C4225214,,,,,,,,
mondo:0014766,leukodystrophy and acquired microcephaly with or without dystonia;,"['leukodystrophy and acquired microcephaly with or without dystonia', 'LDAMD']",,616763,,C4225213,,,,,,,,
mondo:0014767,Seckel syndrome 9,"['Seckel syndrome type 9', 'TRAIP Seckel syndrome', 'Seckel syndrome caused by mutation in TRAIP', 'Seckel syndrome 9', 'SCKL9']",0070005,616777,,C4225212,,,,,,,,
mondo:0014768,"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2","['CADASIL caused by mutation in HTRA1', 'CADASIL type 2', 'HTRA1 CADASIL', 'autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 2', 'CADASIL 2', 'cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2', 'CADASIL2']",0111036,616779,,C4225211,,,,,,,,
mondo:0014769,inherited oocyte maturation defect,"['oocyte maturation defect', 'OOMD']",,,,CN238505,"['-0.094', '0.04684', '0.02052', '-0.05646', '0.0718', '-0.0881', '-0.01362', '0.1333', '-0.0567', '-0.0393', '-0.01689', '-0.06287', '0.02357', '0.02202', '-0.02795', '-0.0472', '0.005028', '-0.01409', '-0.06696', '-0.1957', '-0.002584', '-0.04572', '0.1058', '-0.02821', '0.03925', '-0.02611', '-0.002954', '-0.006565', '0.02797', '-0.0729', '0.09576', '0.003159', '0.09406', '0.06396', '-0.0132', '-0.01622', '0.04474', '-0.04538', '-0.01826', '-0.0944', '0.04507', '-0.0631', '0.0248', '-0.01846', '-0.008255', '-0.1213', '-0.01855', '0.02173', '0.05255', '0.063', '0.002893', '-0.0525', '-0.01498', '0.03314', '-0.05438', '-0.04178', '0.09283', '-0.01715', '-0.1068', '0.0093', '0.0491', '0.06635', '0.02069', '0.00599', '0.0239', '0.02586', '0.1011', '0.05002', '-0.0968', '0.075', '-0.09393', '0.002964', '0.03946', '-0.02417', '0.0324', '0.04617', '0.03586', '-0.02855', '-0.069', '-0.0166', '-0.01555', '0.02681', '0.001485', '0.03632', '-0.0186', '-0.02965', '0.07684', '0.0542', '0.07776', '0.01442', '-0.00011605', '0.057', '-0.002243', '0.02605', '0.1616', '0.05658', '0.1382', '-0.1508', '0.0192', '0.0195']",,,,,,,
mondo:0014770,Joubert syndrome 25,"['Joubert syndrome caused by mutation in CEP104', 'JBTS25', 'Joubert syndrome 25', 'CEP104 Joubert syndrome', 'Joubert syndrome type 25']",0110994,616781,,C4084842,,,,,,,,
mondo:0014771,Joubert syndrome 26,"['Joubert syndrome caused by mutation in KIAA0556', 'Joubert syndrome type 26', 'Joubert syndrome 26', 'KIAA0556 Joubert syndrome', 'JBTS26']",0110995,616784,,C4084843,,,,,,,,
mondo:0014772,orofacial cleft 15,"['orofacial cleft type 15', 'cleft lip/palate caused by mutation in DLX4', 'DLX4 cleft lip/palate', 'OFC15', 'orofacial cleft 15']",0080408,616788,,,,,,,,,,
mondo:0014773,cardiac anomalies - developmental delay - facial dysmorphism syndrome,"['intellectual disability and distinctive FACIAL features with or without CARDIAC defects', 'impaired intellectual development and distinctive facial features with or without cardiac defects', 'mental retardation and distinctive FACIAL features with or without CARDIAC defects', 'cardiac anomalies - developmental delay - facial dysmorphism syndrome', 'intellectual disability and distinctive Facial features with or without Cardiac defects', 'mental retardation and distinctive Facial features with or without Cardiac defects', 'MED13L haploinsufficiency syndrome', 'MRFACD', 'intellectual disability and distinctive facial features with or without cardiac defects', 'MED13L syndrome']",,616789,369891,C4225208,"['-0.2944', '-0.0504', '0.2306', '-0.2842', '0.079', '-0.11725', '0.4014', '0.8115', '-0.843', '-0.06964', '-0.1814', '-0.5264', '0.4268', '-0.1045', '0.08496', '0.05484', '0.00613', '-0.4573', '-0.3093', '-0.3867', '0.3745', '0.3406', '-0.2125', '-0.12415', '-0.00501', '-0.6387', '-0.1234', '0.1619', '0.4407', '-0.3691', '0.263', '-0.0879', '0.5654', '0.2537', '0.009834', '-0.241', '-0.2656', '-0.2418', '-0.54', '-0.699', '0.3096', '0.02007', '-0.07367', '-0.169', '-0.3289', '-0.3506', '-0.12115', '0.4468', '-0.528', '0.02885', '-0.276', '-0.01567', '-0.2026', '0.0321', '-0.4646', '-0.04724', '-0.2339', '0.1213', '0.02902', '-0.03864', '-0.0732', '0.2156', '-0.2152', '0.1544', '-0.0812', '-0.2788', '0.3518', '0.3374', '0.04886', '0.2756', '-0.1548', '0.1921', '-0.2084', '0.0425', '0.0474', '0.17', '0.4666', '-1.107', '-0.2808', '0.1527', '0.4207', '0.0622', '-0.1915', '0.8467', '0.1573', '0.512', '-0.1031', '0.2854', '0.2155', '0.4302', '0.2832', '0.3203', '-0.0871', '0.2338', '0.9775', '0.06024', '0.1951', '-0.2273', '0.5493', '0.4407']",,,,,,,
mondo:0014774,"neuroblastoma, susceptibility to, 7","['neuroblastoma, susceptibility to, type 7', 'neuroblastoma, susceptibility to, 7', 'NBLST7']",,616792,,,,,,,,,,
mondo:0014775,combined oxidative phosphorylation deficiency 28,"['neonatal severe cardiopulmonary failure due to mitochondrial methylation defect', 'COXPD28', 'combined oxidative phosphorylation deficiency type 28', 'combined oxidative phosphorylation defect type 28', 'combined oxidative phosphorylation deficiency 28', 'SLC25A26 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency caused by mutation in SLC25A26']",0111470,616794,466784,C4225206,,,,,,,,
mondo:0014776,spinocerebellar ataxia type 42,"['SCA42', 'spinocerebellar ataxia 42', 'spinocerebellar ataxia type 42']",0111742,616795,458803,C4225205,"['-0.02275', '0.079', '-0.06064', '-0.0193', '-0.01654', '-0.1394', '-0.02336', '0.07007', '-0.1289', '-0.04764', '-0.03748', '-0.01773', '-0.05087', '-0.00452', '0.06305', '-0.07214', '0.003416', '-0.04498', '0.013794', '-0.131', '-0.03757', '-0.04544', '-0.005684', '-0.0469', '0.02443', '-0.011246', '-0.01833', '-0.07666', '0.01106', '-0.0454', '0.01598', '0.03302', '0.1145', '0.02492', '-0.0049', '-0.0891', '-0.0143', '-0.06616', '-0.0832', '-0.04895', '0.0003333', '-0.08295', '0.01251', '0.01307', '-0.0128', '-0.1317', '-0.03522', '0.09424', '0.01098', '-0.066', '-0.00503', '0.03214', '-0.04144', '-0.03656', '-0.059', '-0.06464', '0.10815', '-0.05637', '-0.1225', '-0.0008373', '0.06058', '0.01063', '0.008255', '0.04453', '-0.05182', '0.0001073', '0.10645', '0.0441', '-0.10065', '0.127', '-0.00787', '0.03033', '0.007347', '-0.1154', '0.09985', '0.0872', '-0.02321', '-0.01637', '-0.03094', '0.009315', '-0.01848', '-0.02165', '-0.03418', '0.0575', '-0.010185', '0.002663', '0.03084', '0.0794', '0.11163', '0.010544', '0.0419', '0.07745', '0.0323', '-0.00223', '0.2224', '0.0753', '0.05945', '-0.0475', '0.0158', '0.0501']",C171269,0009059,,,,,
mondo:0014777,"hypotonia, infantile, with psychomotor retardation and characteristic facies 2","['IHPRF2', 'hypotonia, infantile, with psychomotor retardation and characteristic facies caused by mutation in UNC80', 'hypotonia, infantile, with psychomotor retardation and characteristic facies type 2', 'UNC80 hypotonia, infantile, with psychomotor retardation and characteristic facies', 'hypotonia, infantile, with psychomotor retardation and characteristic facies 2']",,616801,,C4225203,,,,,,,,
mondo:0014778,Lamb-Shaffer syndrome,"['LAMSHF', 'Lamb-Shaffer syndrome']",,616803,530983,C4225202,,,,,,,,
mondo:0014779,Wilms tumor 6,"['Wilms tumor 6', 'Wilms tumor 6, susceptibility to', 'WT6', 'Wilms tumour 6; WT6', 'Wilms tumour 6, susceptibility to', 'Wilms tumor type 6', 'Wilms tumour type 6']",,616806,,,,,,,,,,
mondo:0014780,hyperphosphatasia with intellectual disability syndrome 6,"['hyperphosphatasia with intellectual disability syndrome type 6', 'glycosylphosphatidylinositol biosynthesis defect 12', 'hyperphosphatasia with intellectual disability syndrome 6', 'hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGY', 'PIGY hyperphosphatasia-intellectual disability syndrome', 'hyperphosphatasia with mental retardation syndrome 6', 'hyperphosphatasia with mental retardation syndrome type 6', 'HPMRS6']",,616809,,C4225201,,,,,,,,
mondo:0014781,combined oxidative phosphorylation deficiency 29,"['combined oxidative phosphorylation deficiency caused by mutation in TXN2', 'TXN2 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency type 29', 'COXPD29', 'combined oxidative phosphorylation deficiency 29']",0111501,616811,478029,C4225200,,,,,,,,
mondo:0014782,autosomal recessive limb-girdle muscular dystrophy type 2X,"['BVES autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, limb-girdle, type 2x', 'muscular dystrophy, limb-girdle, autosomal recessive 25', 'autosomal recessive limb-girdle muscular dystrophy-cardiac arrhythmia syndrome', 'LGMD2X', 'muscular dystrophy, limb-girdle, type 2X', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in BVES']",0110290,616812,476084,C4225199,,,,,,,,
mondo:0014784,severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome,"['hypotonia, infantile, with psychomotor retardation', 'IHPMR']",,616816,467176,C4225196,,,,,,,,
mondo:0014785,"microcephaly, short stature, and impaired glucose metabolism 2","['microcephaly, short stature, and impaired glucose metabolism type 2', 'PPP1R15B microcephaly, short stature, and impaired glucose metabolism', 'MSSGM2', 'microcephaly, short stature, and impaired glucose metabolism caused by mutation in PPP1R15B', 'microcephaly, short stature, and impaired glucose metabolism 2']",,616817,,C4225195,,,,,,,,
mondo:0014786,"IgA nephropathy, susceptibility to, 3","['SPRY2 IgA glomerulonephritis', 'IGAN3', 'susceptibility to IgA nephropathy 3', 'IgA glomerulonephritis caused by mutation in SPRY2', 'IgA nephropathy, susceptibility to, 3', 'IgA nephropathy, susceptibility to, type 3']",,616818,,,,,,,,,,
mondo:0014787,severe intellectual disability-corpus callosum agenesis-facial dysmorphism-cerebellar ataxia syndrome,"['Birk-Flusser syndrome', 'corpus callosum, agenesis OF, with FACIAL anomalies and cerebellar ataxia', 'CCAFCA', 'corpus callosum, agenesis of, with Facial anomalies and cerebellar ataxia']",,616819,466688,C4225193,,,,,,,,
mondo:0014788,autosomal recessive limb-girdle muscular dystrophy type 2W,"['autosomal recessive limb-girdle muscular dystrophy caused by mutation in LIMS2', 'LIMS2 autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, autosomal recessive, with cardiomyopathy and triangular tongue', 'LGMD2W', 'muscular dystrophy, limb-girdle, type 2W', 'muscular dystrophy, limb-girdle, type 2w']",0110288,616827,466801,C4225192,,,,,,,,
mondo:0014789,CCDC115-CDG,"['CDG syndrome type IIo', 'CDG2O', 'congenital disorder of glycosylation type IIo', 'congenital disorder of glycosylation, type IIo', 'CDG-IIo', 'carbohydrate deficient glycoprotein syndrome type IIo', 'CDG IIo', 'congenital disorder of glycosylation type 2o']",0070267,616828,468684,,,,,,,,,
mondo:0014790,TMEM199-CDG,"['congenital disorder of glycosylation type IIp', 'carbohydrate deficient glycoprotein syndrome type IIp', 'CDG IIp', 'congenital disorder of glycosylation, type IIp', 'congenital disorder of glycosylation type 2p', 'CDG-IIp', 'CDG2P', 'CDG syndrome type IIp']",0070268,616829,466703,C4225190,,,,,,,,
mondo:0014791,Luscan-Lumish syndrome,"['LLs', 'SETD2-related overgrowth syndrome', 'Luscan-Lumish syndrome']",,616831,597738,C4085873,"['-0.01646', '0.03488', '0.00953', '-0.006176', '0.006256', '-0.0483', '-7.415e-05', '0.04343', '-0.03894', '-0.02461', '-0.01294', '-0.01611', '-0.010826', '0.01743', '-0.01096', '-0.01689', '-0.001348', '-0.01282', '-0.01608', '-0.0717', '-0.0068', '-0.02463', '0.03119', '-0.02063', '0.01311', '-0.015', '-0.02509', '-0.003294', '0.014114', '-0.0187', '0.02164', '-0.01252', '0.03455', '0.01392', '0.001608', '-0.00914', '0.0001404', '-0.0329', '0.0006976', '-0.04327', '0.01511', '-0.03125', '0.00531', '-0.0316', '0.001307', '-0.03537', '-0.02214', '0.00893', '0.00851', '0.01059', '-0.00924', '-0.00863', '0.00924', '-0.0091', '-0.0212', '-0.00656', '0.01636', '-0.01345', '-0.0385', '-0.003191', '0.01863', '0.011635', '-0.005486', '0.013954', '-0.005657', '0.013084', '0.0369', '0.01421', '-0.04147', '0.0429', '-0.03928', '0.00405', '0.003653', '-0.01547', '0.0087', '0.01973', '0.0122', '0.00905', '-0.0192', '-0.01651', '0.00816', '0.01311', '-0.006313', '0.02188', '0.007236', '0.008545', '0.02266', '0.05096', '0.04413', '0.02397', '-0.001005', '0.03586', '0.0004306', '0.01277', '0.06445', '0.002375', '0.03168', '-0.05322', '-0.000749', '0.01358']",,,,,,,
mondo:0014792,Paget disease of bone 6,"['Paget disease of bone type 6', 'Paget disease of bone 6', 'PDB6']",0081369,616833,,C4085250,,,,,,,,
mondo:0014793,microcephaly-congenital cataract-psoriasiform dermatitis syndrome,"['MCCPD', 'sterol-C4-methyl oxidase deficiency', 'smo deficiency', 'Sc4Mol deficiency', 'microcephaly, congenital cataract, and psoriasiform dermatitis']",,616834,488168,C4225189,,,,,,,,
mondo:0014794,Meier-Gorlin syndrome 6,"['Meier-GORLIN syndrome 6', 'Meier-Gorlin syndrome 6', 'MGORS6', 'Meier-Gorlin syndrome type 6', 'Meier-Gorlin syndrome caused by mutation in GMNN', 'GMNN Meier-Gorlin syndrome']",0080517,616835,,C4225188,,,,,,,,
mondo:0014795,"exercise intolerance, riboflavin-responsive","['exercise intolerance, riboflavin-responsive', 'RREI']",,616839,,C4225187,"['-0.03186', '0.0667', '-0.001427', '0.01468', '0.001528', '-0.0931', '0.0219', '0.1213', '-0.0708', '-0.02213', '-0.01587', '0.0198', '0.00845', '0.04932', '-0.02867', '-0.02342', '-0.01584', '-0.02148', '-0.0826', '-0.1192', '0.01709', '-0.03647', '0.0127', '0.008934', '0.001248', '-0.0376', '-0.01794', '-0.03186', '-0.00634', '-0.0493', '0.05286', '-0.014404', '0.08', '0.00916', '0.002222', '-0.02957', '-0.03857', '-0.01805', '0.001422', '-0.04758', '0.0329', '-0.0728', '0.0414', '0.012985', '0.00678', '-0.03314', '0.00668', '0.04343', '0.0177', '0.0676', '-0.04492', '0.00201', '0.03983', '0.006298', '-0.03378', '-0.02234', '0.0883', '-0.0399', '-0.0705', '-0.03038', '0.06824', '0.01534', '0.01134', '-0.0308', '-0.01442', '0.0148', '0.0954', '0.075', '-0.03827', '0.05743', '-0.0468', '0.056', '0.00912', '-0.02928', '0.0398', '0.0713', '-0.004925', '-0.02309', '-0.02382', '0.01883', '-0.015465', '-0.02411', '-0.00759', '0.0348', '0.013145', '0.03894', '0.03452', '0.01662', '0.11957', '0.00682', '0.02873', '0.02646', '-0.02534', '0.006805', '0.1361', '0.05814', '0.02573', '-0.0541', '-0.04648', '0.00348']",,,,,,,
mondo:0014796,autosomal recessive early-onset Parkinson disease 23,"['autosomal recessive early-onset Parksinson disease type 23', 'young-onset Parkinson disease caused by mutation in VPS13C', 'Parkinson disease 23, autosomal recessive, early onset', 'VPS13C young-onset Parkinson disease', 'Parkinson disease 23, autosomal recessive early-onset', 'autosomal recessive early-onset Parkinson disease 23', 'PARK23', 'autosomal recessive early-onset Parkinson^s disease 23']",0060896,616840,,C4225186,,,,,,,,
mondo:0014797,lymphatic malformation 6,"['lymphedema, hereditary, type III', 'generalised lymphatic dysplasia of Fotiou', 'generalized lymphatic dysplasia of Fotiou', 'lymphedema, hereditary, 3', 'lymphedema, hereditary, III', 'LMPH3']",,616843,,C4225184,"['0.5923', '-0.273', '-0.324', '0.1674', '-0.2993', '-1.014', '0.3098', '0.12335', '-0.332', '-0.3127', '0.368', '1.439', '-0.015526', '1.077', '-0.2583', '0.0966', '-0.3284', '-0.2095', '-0.4783', '-0.327', '0.10565', '-0.03754', '0.1783', '0.235', '0.013985', '-0.0632', '-0.3477', '0.7256', '0.5967', '0.06946', '-0.556', '0.293', '0.5205', '-0.2517', '0.1948', '0.38', '-0.3584', '0.01762', '0.8486', '-0.677', '0.1833', '0.4368', '0.7144', '0.06', '0.166', '-0.0629', '-0.469', '-0.7407', '1.054', '-0.2822', '-0.1393', '-0.3706', '0.7124', '0.386', '-0.8267', '-0.1498', '0.1624', '-0.784', '-0.8726', '-0.74', '-0.1704', '0.3992', '-0.393', '-0.0393', '-0.577', '0.7036', '0.6885', '0.9487', '-1.014', '-0.3706', '-0.729', '0.2347', '-0.2039', '-0.753', '0.4229', '0.07135', '-0.695', '0.909', '0.1241', '-0.4138', '-0.2817', '0.758', '-0.274', '0.4468', '0.738', '-0.2272', '-0.4517', '-0.657', '0.08813', '-0.1289', '-0.1987', '0.6963', '-0.503', '0.541', '1.421', '0.4478', '0.516', '-0.217', '-0.10114', '0.1243']",,0009153,,,,,
mondo:0014798,brachydactyly type A1D,"['brachydactyly, type A1, D', 'BMPR1B brachydactyly type A1', 'brachydactyly type A1 caused by mutation in BMPR1B', 'BDA1D']",0110978,616849,,C4225183,,,,,,,,
mondo:0014799,cataract 45,"['cataract 45', 'SIPA1L3 early-onset non-syndromic cataract', 'cataract type 45', 'CTRCT45', 'early-onset non-syndromic cataract caused by mutation in SIPA1L3']",0110262,616851,,C4225182,,,,,,,,
mondo:0014800,progressive scapulohumeroperoneal distal myopathy,"['myopathy, scapulohumeroperoneal', 'SHPM']",,616852,447977,C4225181,,,,,,,,
mondo:0014801,even-plus syndrome,"['epiphysial-vertebral-ear dysplasia-nose-plus associated findings syndrome', 'even-plus syndrome', 'EVPLS', 'epiphyseal and vertebral dysplasia, microtia, and flat Nose, plus associated malformations']",,616854,496751,C4225180,"['-0.01048', '0.02434', '-0.006363', '-0.002481', '0.013954', '-0.0335', '0.001277', '0.04468', '-0.02089', '-0.01167', '-0.0131', '-0.0004096', '0.004112', '0.01227', '-0.0206', '-0.01444', '0.00829', '-0.014946', '-0.02634', '-0.048', '-0.006546', '-0.006706', '0.03244', '-0.01155', '0.01662', '-0.0134', '-0.01478', '-0.012596', '0.005875', '-0.01852', '0.0315', '-0.013214', '0.02191', '0.02895', '0.003788', '-0.010376', '-0.01097', '-0.0265', '-0.0044', '-0.04337', '0.01988', '-0.02052', '0.008675', '-0.01947', '0.006832', '-0.02086', '-0.02553', '0.01726', '0.0002153', '0.01054', '-0.01642', '-0.005844', '0.00898', '0.0008483', '-0.01926', '-0.009125', '0.0276', '-0.009155', '-0.0406', '0.00857', '0.01753', '0.01625', '-0.007168', '-0.0003211', '0.003614', '-0.004524', '0.03027', '0.01288', '-0.02536', '0.03403', '-0.03735', '0.01132', '0.015045', '-0.01511', '0.01706', '0.0173', '-0.01125', '-0.004215', '-0.02878', '-0.02231', '0.01758', '0.01089', '-0.01938', '0.0294', '0.00428', '0.004784', '-0.0006633', '0.03564', '0.0417', '-0.004257', '0.01521', '0.02585', '-0.0001897', '0.01436', '0.06207', '0.02077', '0.0376', '-0.04425', '-0.0002682', '0.01277']",,,,,,,
mondo:0014802,Cowden syndrome 7,"['SEC23B Cowden disease', 'CWS7', 'Cowden disease caused by mutation in SEC23B', 'Cowden syndrome 7', 'Cowden syndrome type 7']",0081003,616858,,C4225179,,,,,,,,
mondo:0014803,spasticity-ataxia-gait anomalies syndrome,"['childhood-onset spasticity with variant non-ketotic hyperglycinemia', 'spasticity, childhood-onset, with hyperglycinemia', 'SPAHGC', 'childhood-onset spasticity with hyperglycinemia']",,616859,401866,C4225178,"['-0.3594', '-0.224', '-0.137', '0.004906', '-0.3127', '-0.99', '0.01329', '-0.0904', '-0.766', '-0.8774', '0.0631', '0.1488', '-0.1625', '0.1875', '0.5864', '-0.3135', '0.01602', '-0.331', '0.06232', '-0.984', '-0.04108', '-0.3276', '0.2054', '-0.4697', '0.4802', '-0.4155', '-0.3315', '0.4075', '-0.1593', '-0.918', '0.1678', '0.5293', '-0.5786', '-0.034', '0.3264', '0.09296', '-0.2356', '0.2866', '0.6426', '0.3489', '0.4023', '0.1915', '-0.4907', '0.4763', '0.5337', '-0.506', '0.0588', '0.3755', '0.4983', '0.1134', '-0.3801', '0.2148', '-0.1685', '-0.346', '-0.05667', '-0.83', '0.4067', '0.5737', '-0.12115', '0.612', '-0.6353', '0.2988', '0.3035', '-0.09644', '-0.4768', '0.739', '0.298', '0.599', '-0.6147', '0.518', '0.7793', '0.65', '-0.0755', '-0.632', '0.7935', '0.2578', '0.2466', '0.326', '0.1392', '0.561', '-0.3274', '-0.71', '0.602', '1.082', '-0.2379', '-0.5034', '0.4207', '-0.1467', '0.494', '0.597', '0.501', '0.4219', '0.228', '0.0224', '1.102', '1.067', '0.4707', '0.6436', '-0.4622', '0.01055']",,,,,,,
mondo:0014804,sideroblastic anemia 3,"['GLRX5-related sideroblastic anaemia', 'adult-onset autosomal recessive sideroblastic anaemia', 'adult-onset autosomal recessive sideroblastic anemia', 'SIDBA3', 'anemia, sideroblastic, 3, pyridoxine-refractory', 'GLRX5-related sideroblastic anemia']",0080343,616860,255132,,"['-0.3591', '0.405', '-0.1114', '0.1353', '0.6484', '0.1416', '-0.3718', '0.4038', '-0.2554', '-0.5054', '0.7695', '-0.03192', '0.2068', '0.4746', '-1.1', '0.02676', '-0.666', '0.1488', '-0.4614', '-0.5845', '-0.2898', '-0.5317', '0.33', '-0.471', '0.7153', '-0.3894', '-0.1259', '-0.3342', '0.579', '-0.06964', '0.1862', '0.3572', '0.4558', '0.5513', '0.5093', '-0.196', '-0.9346', '-0.529', '0.671', '-0.1338', '-0.716', '0.264', '-0.1012', '-0.4077', '-0.8125', '-1.016', '0.10785', '0.1361', '0.388', '-0.3342', '0.4995', '0.3208', '0.776', '-0.1656', '0.5376', '-0.7686', '0.1444', '0.358', '-1.017', '0.01584', '-0.0449', '0.3523', '-0.2079', '-0.3', '-0.2263', '0.2905', '0.3738', '0.716', '-0.5576', '0.864', '0.8496', '-0.2258', '-0.551', '-0.6494', '0.335', '1.0205', '0.3086', '0.2537', '0.0905', '0.3188', '0.002514', '-0.05594', '0.02817', '0.1357', '0.691', '-0.4272', '-0.575', '0.396', '0.543', '-0.1338', '0.6436', '0.306', '-0.2091', '-0.2113', '0.644', '1.047', '0.2974', '-0.0751', '0.11707', '-0.5415']",,,,,,,
mondo:0014805,Hao-Fountain syndrome,"['HAFOUS', 'USP7-related neurodevelopmental disorder']",,616863,643549,C4225667,,,,,,,,
mondo:0014806,spinal muscular atrophy with congenital bone fractures 1,"['SMA1 with congenital bone fractures', 'TRIP4 prenatal-onset spinal muscular atrophy with congenital bone fractures', 'SMABF1', 'spinal muscular atrophy with congenital bone fractures 1', 'spinal muscular atrophy with congenital bone fractures type 1', 'prenatal-onset spinal muscular atrophy with congenital bone fractures caused by mutation in TRIP4', 'spinal muscular atrophy, type I, with congenital bone fractures', 'spinal muscular atrophy type 1 with congenital bone fractures']",,616866,,C4225177,"['-0.0719', '0.0928', '0.0826', '-0.0607', '0.0786', '-0.1204', '0.00981', '0.1981', '-0.1719', '-0.05905', '-0.03897', '-0.03235', '-0.03616', '0.01918', '0.007797', '-0.0599', '0.00155', '-0.0664', '-0.05484', '-0.1995', '-0.003149', '-0.09174', '0.09393', '-0.0638', '-0.01619', '-0.06506', '0.01756', '-0.05942', '-0.0557', '-0.0493', '0.05136', '-0.011314', '0.1224', '0.0569', '-0.00997', '-0.015205', '0.005802', '-0.03662', '-0.006535', '-0.11414', '-0.00915', '-0.129', '0.001405', '-0.02013', '-0.07465', '-0.0782', '0.008934', '0.10455', '0.05264', '0.02917', '-0.04886', '-0.01869', '0.06396', '-0.001352', '-0.04895', '-0.0845', '0.08417', '-0.0363', '-0.0835', '-0.01128', '0.0658', '0.04156', '-0.031', '0.002213', '-0.0809', '0.04034', '0.1122', '0.1779', '-0.10724', '0.0825', '-0.05167', '0.006535', '0.0347', '-0.143', '0.0757', '0.0533', '0.02774', '-0.013435', '-0.0798', '-0.0718', '-0.03638', '-0.02301', '-0.015434', '0.1676', '-0.1193', '0.02544', '0.0728', '0.1048', '0.1504', '-0.0203', '0.028', '0.10046', '0.0326', '0.04913', '0.2098', '0.06186', '0.1731', '-0.0894', '0.00972', '0.02702']",,,C564805,,,,
mondo:0014807,spinal muscular atrophy with congenital bone fractures 2,"['spinal muscular atrophy with congenital bone fractures type 2', 'spinal muscular atrophy with congenital bone fractures 2', 'ASCC1 prenatal-onset spinal muscular atrophy with congenital bone fractures', 'prenatal-onset spinal muscular atrophy with congenital bone fractures caused by mutation in ASCC1', 'SMABF2']",,616867,,C4225176,"['-0.04538', '0.0629', '0.03506', '-0.0375', '0.02858', '-0.10284', '0.00909', '0.11774', '-0.1072', '-0.02974', '-0.032', '-0.006405', '-0.01564', '0.0249', '-0.02148', '-0.05453', '-0.00592', '-0.027', '-0.0328', '-0.14', '0.01057', '-0.04178', '0.06586', '-0.02391', '0.0157', '-0.02399', '0.01198', '-0.03137', '-0.02869', '-0.02704', '0.04416', '-0.013016', '0.08826', '0.03598', '0.00817', '-0.02777', '-0.0199', '-0.03235', '-0.01473', '-0.0816', '0.01278', '-0.09155', '0.0003989', '-0.002422', '-0.01866', '-0.05283', '0.002773', '0.07025', '0.02481', '0.02675', '-0.0192', '-0.01689', '0.03665', '0.00143', '-0.0445', '-0.0603', '0.0639', '-0.03622', '-0.0632', '-0.01304', '0.05142', '0.01936', '-0.01611', '0.000588', '-0.039', '0.01504', '0.0785', '0.09705', '-0.0788', '0.0707', '-0.04538', '0.01666', '0.02937', '-0.08966', '0.05545', '0.02425', '0.01013', '0.00707', '-0.0439', '-0.0555', '-0.005817', '-0.006287', '-0.00813', '0.0987', '-0.0682', '0.01619', '0.03696', '0.06616', '0.1005', '-0.01619', '0.028', '0.0668', '0.02571', '0.02988', '0.1304', '0.04776', '0.09717', '-0.0817', '-0.002487', '0.01807']",,,,,,,
mondo:0014808,congenital secretory sodium diarrhea 8,"['SLC9A3 secretory diarrhea', 'congenital secretory sodium diarrhoea type 8', 'diarrhea, congenital sodium', 'SLC9A3 secretory diarrhoea', 'diarrhoea 8, secretory sodium, congenital', 'secretory diarrhea caused by mutation in SLC9A3', 'secretory diarrhoea caused by mutation in SLC9A3', 'DIAR8', 'diarrhea 8, secretory sodium, congenital', 'congenital secretory sodium diarrhea type 8']",0060777,616868,,CN515063,,,,,,,,
mondo:0014809,DDX41-related hematologic malignancy predisposition syndrome,"['susceptibility to familial (multiple types) myeloproliferative/lymphoproliferative neoplasms', 'DDX41 hereditary neoplastic syndrome', 'myeloproliferative/lymphoproliferative neoplasms, familial (multiple types), susceptibility to', 'hereditary neoplastic syndrome caused by mutation in DDX41', 'MPLPF']",,616871,488647,,,,,,,,,
mondo:0014810,pancytopenia due to IKZF1 mutations,"['Cid due to IKAROS deficiency', 'immunodeficiency, common variable, type 13', 'IKZF1 syndrome with combined immunodeficiency', 'combined immunodeficiency due to IKAROS deficiency', 'immunodeficiency, common variable, 13', 'syndrome with combined immunodeficiency caused by mutation in IKZF1', 'CVID13']",0081155,616873,317473,C4225173,"['-0.3223', '0.2373', '-0.0733', '0.06934', '0.152', '-0.2673', '0.1422', '0.01446', '-0.176', '-0.09845', '-0.09924', '-0.01451', '-0.1735', '0.0677', '0.01013', '-0.259', '-0.2039', '0.1164', '-0.2617', '-0.3687', '0.01968', '-0.1941', '0.426', '-0.0884', '0.2026', '0.0733', '-0.1709', '0.00863', '-0.2502', '-0.2323', '0.2443', '0.2238', '0.4128', '0.1497', '-0.06415', '-0.221', '-0.2328', '-0.0752', '-0.2734', '-0.1246', '-0.0339', '-0.1996', '0.12415', '-0.1917', '-0.4282', '-0.193', '-0.1874', '-0.312', '0.2057', '0.004128', '-0.04733', '-0.151', '0.2905', '-0.0656', '-0.0365', '-0.1011', '0.1431', '-0.1747', '-0.0702', '0.12286', '0.0578', '0.2637', '0.2844', '-0.0772', '0.2966', '0.1879', '0.204', '0.396', '-0.4229', '0.3027', '-0.3188', '-0.07385', '-0.007618', '-0.01797', '0.26', '-0.3037', '0.3696', '0.1231', '0.1704', '0.04965', '-0.0939', '-0.02438', '0.001555', '0.0285', '-0.01114', '-0.01607', '0.262', '0.3103', '0.3657', '0.0691', '0.3438', '0.2854', '-0.1276', '-0.2375', '0.622', '0.4915', '0.319', '-0.4944', '0.009605', '0.15']",,,,,,,
mondo:0014811,"cerebellar atrophy, visual impairment, and psychomotor retardation;","['CAVIPMR', 'cerebellar atrophy, visual impairment, and psychomotor retardation']",0081276,616875,,C4225172,,,,,,,,
mondo:0014813,hypomyelinating leukodystrophy 13,"['HLD13', 'leukodystrophy caused by mutation in hikeshi', 'hypomyelinating leukodystrophy type 13', 'hikeshi leukodystrophy', 'leukodystrophy, hypomyelinating, 13', 'leukodystrophy, hypomyelinating, type 13', 'HIKESHI leukodystrophy']",0060795,616881,,C4225170,"['0.002169', '0.0141', '-0.00799', '0.00555', '0.00847', '-0.006542', '-0.006187', '0.02405', '-0.01862', '-0.01289', '-0.00713', '-0.00789', '-0.00754', '-0.001608', '0.006092', '-0.01736', '0.002277', '-0.01481', '0.003414', '-0.0264', '0.002592', '-0.008064', '0.007755', '-0.00661', '-0.000418', '-0.01479', '-0.002134', '0.002163', '0.00434', '-0.006805', '0.0144', '-0.008606', '0.007584', '0.001874', '-0.003366', '-0.001439', '0.00595', '-0.00915', '0.002316', '-0.003323', '0.014885', '-0.0119', '0.00655', '-0.01322', '-0.00659', '-0.010994', '-0.001036', '0.0002102', '-0.01011', '-0.004658', '0.007786', '0.003202', '0.002096', '0.003698', '-0.005024', '-0.01186', '0.00531', '0.002735', '-0.01326', '0.00593', '0.004726', '0.01236', '-0.002125', '-0.003326', '0.004105', '0.006317', '0.00706', '0.003689', '-0.02238', '0.011696', '-0.01913', '-0.000631', '0.01025', '-0.0127', '0.01206', '0.01137', '-0.0007153', '-0.0007277', '-0.01527', '-0.01172', '0.00647', '0.00663', '-0.001387', '0.01517', '-0.01095', '-0.0004005', '0.00766', '0.004063', '0.013504', '0.00996', '0.003784', '0.01657', '0.007664', '0.013435', '0.03174', '0.014145', '0.01028', '-0.01273', '0.008484', '0.01306']",,,,,,,
mondo:0014814,advanced sleep phase syndrome 3,"['PER3 advanced sleep phase syndrome', 'familial advanced sleep phase syndrome 3', 'advanced sleep phase syndrome type 3', 'advanced sleep phase syndrome caused by mutation in PER3', 'FASPS3', 'advanced sleep phase syndrome, familial, 3', 'advanced sleep phase syndrome, familial, type 3']",0110013,616882,,C4225169,,,,,,,,
mondo:0014815,"intellectual disability, autosomal recessive 52","['LMAN2L autosomal recessive non-syndromic intellectual disability', 'intellectual developmental disorder, autosomal recessive 52', 'intellectual disability, autosomal recessive type 52', 'autosomal recessive non-syndromic intellectual disability caused by mutation in LMAN2L', 'intellectual disability, autosomal recessive 52', 'mental retardation, autosomal recessive 52', 'mental retardation, autosomal recessive type 52', 'MRT52']",0081215,616887,,C4225168,,,,,,,,
mondo:0014816,split-foot malformation-mesoaxial polydactyly syndrome,"['split-foot malformation with mesoaxial polydactyly', 'split-foot malformation-mesoaxial polydactyly-nail abnormalities-sensorineural hearing loss syndrome', 'SFMMP']",,616890,488232,C4225167,,,,,,,,
mondo:0014817,"nephrotic syndrome, type 12","['familial nephrotic syndrome caused by mutation in NUP93', 'nephrotic syndrome, type 12', 'NPHS12', 'NUP93 familial nephrotic syndrome']",0080387,616892,,C4225166,,,,,,,,
mondo:0014818,"nephrotic syndrome, type 13","['nephrotic syndrome, type 13', 'familial nephrotic syndrome caused by mutation in NUP205', 'NPHS13', 'NUP205 familial nephrotic syndrome']",0080381,616893,,C4225165,,,,,,,,
mondo:0014819,autosomal dominant Robinow syndrome 3,"['Robinow syndrome, autosomal dominant 3', 'autosomal dominant Robinow syndrome type 3', 'DVL3 Robinow syndrome', 'DRS3', 'Robinow syndrome caused by mutation in DVL3', 'Robinow syndrome, autosomal dominant type 3']",0060767,616894,,C4225164,,,,,,,,
mondo:0014820,mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type),"['mitochondrial DNA depletion syndrome caused by mutation in OPA1', 'mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type)', 'MTDPS14', 'mitochondrial DNA depletion syndrome 14 (cardioencephalomyopathic type)', 'OPA1 mitochondrial DNA depletion syndrome']",0080336,616896,,C4225163,"['-0.1172', '0.1246', '0.03998', '0.03314', '0.06573', '-0.1779', '0.007206', '0.1263', '-0.10864', '-0.0653', '0.00288', '-0.0174', '0.0717', '0.002178', '-0.04855', '-0.10223', '-0.03473', '-0.05856', '-0.0419', '-0.2023', '-0.002728', '-0.0809', '0.1046', '-0.04282', '0.0541', '0.01682', '-0.04697', '-0.00834', '-0.02072', '-0.035', '0.08185', '0.05182', '0.1732', '0.01863', '-0.02914', '-0.08527', '-0.0679', '-0.1078', '-0.03885', '-0.1028', '0.07324', '-0.1559', '-0.00223', '0.006226', '-0.0498', '-0.1007', '-0.01756', '0.03476', '0.0779', '-0.01065', '-0.07324', '-0.0609', '-0.0298', '-0.0216', '-0.02943', '-0.091', '0.1316', '-0.0609', '-0.1222', '0.06137', '0.0984', '-0.001206', '0.03857', '-0.012924', '-0.03476', '0.01279', '0.1265', '0.07416', '-0.1818', '0.1582', '-0.09406', '0.002045', '0.013245', '-0.0291', '0.067', '0.09686', '-0.0442', '0.01622', '-0.1497', '-0.0346', '0.001398', '0.02347', '-0.05103', '0.0804', '-0.014786', '0.01828', '0.10266', '0.165', '0.1531', '0.03192', '0.12415', '0.1111', '-0.02527', '-0.0333', '0.219', '0.1494', '0.0931', '-0.2045', '0.009674', '0.0217']",,,,,,,
mondo:0014821,complex lethal osteochondrodysplasia,"['osteochondrodysplasia, COMPLEX lethal, Symoens-Barnes-Gistelinck type', 'Complex lethal osteochondrodysplasia, Symoens-Barnes-Gistelinck type', 'osteochondrodysplasia, Complex lethal, Symoens-Barnes-Gistelinck type', 'OCLSBG']",,616897,457378,C4225162,,,,,,,,
mondo:0014822,15q14 microdeletion syndrome,"['monosomy 15q14', 'chromosome 15q14 deletion syndrome', 'Del(15)(q14)']",,616898,261190,C4305230,,,,,,,,
mondo:0014823,"hypotonia, infantile, with psychomotor retardation and characteristic facies 3","['IHPRF3', 'TBCK-related intellectual disability syndrome', 'hypotonia, infantile, with psychomotor retardation and characteristic facies type 3', 'hypotonia, infantile, with psychomotor retardation and characteristic facies 3']",,616900,488632,C4225161,,,,,,,,
mondo:0014825,"chromosome 11p13 deletion syndrome, distal",,,616902,,C4311047,,,,,,,,
mondo:0014827,autosomal recessive spastic paraplegia type 76,"['SPG76', 'spastic paraplegia 76, autosomal recessive', 'hereditary spastic paraplegia type 76', 'hereditary spastic paraplegia 76', 'autosomal recessive spastic paraplegia 76', 'autosomal recessive complex spastic paraplegia caused by mutation in CAPN1', 'CAPN1 autosomal recessive complex spastic paraplegia']",0110821,616907,488594,C4310800,"['-0.2246', '0.0193', '0.1631', '-0.446', '-0.2861', '-0.4907', '-0.1522', '0.4512', '-0.6', '-0.0845', '-0.219', '0.1231', '-0.1797', '0.1014', '0.411', '-0.152', '0.1345', '-0.341', '0.0524', '-0.3545', '-0.0204', '-0.04922', '-0.1652', '0.10175', '0.2269', '0.255', '-0.1602', '0.01096', '-0.0895', '-0.1854', '-0.01924', '0.0689', '0.2012', '0.1794', '-0.03342', '-0.4363', '-0.348', '-0.2932', '-0.1615', '-0.2524', '-0.014404', '-0.4307', '-0.1569', '0.4749', '-0.1337', '-0.51', '-0.3733', '0.1943', '0.02014', '0.04407', '-0.17', '0.562', '-0.342', '-0.2717', '-0.1796', '-0.2617', '0.4072', '-0.2786', '-0.2015', '0.0961', '-0.014915', '0.06186', '0.1902', '0.354', '-0.584', '0.06616', '0.3933', '0.4307', '-0.2115', '0.2644', '-0.2925', '0.3784', '0.04697', '-0.4395', '0.553', '0.2103', '0.01083', '0.1757', '0.1965', '-0.2825', '-0.1852', '-0.2937', '0.527', '0.6616', '0.04675', '0.455', '-0.1111', '0.1646', '0.1632', '0.06915', '0.255', '0.3547', '0.1311', '0.1691', '0.699', '0.4297', '0.557', '-0.0736', '0.02272', '0.4128']",,0009019,,,,,
mondo:0014828,immunodeficiency-centromeric instability-facial anomalies syndrome 3,"['CDCA7 immunodeficiency-centromeric instability-facial anomalies syndrome', 'ICF syndrome 3', 'immunodeficiency-centromeric instability-FACIAL anomalies syndrome 3', 'ICF3', 'immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in CDCA7', 'immunodeficiency-centromeric instability-Facial anomalies syndrome 3', 'immunodeficiency-centromeric instability-facial anomalies syndrome type 3', 'immunodeficiency-centromeric instability-Facial anomalies syndrome type 3']",0090010,616910,,C4310799,,,,,,,,
mondo:0014829,immunodeficiency-centromeric instability-facial anomalies syndrome 4,"['HELLS immunodeficiency-centromeric instability-facial anomalies syndrome', 'immunodeficiency-centromeric instability-facial anomalies syndrome type 4', 'immunodeficiency-centromeric instability-FACIAL anomalies syndrome 4', 'immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in HELLS', 'ICF syndrome 4', 'immunodeficiency-centromeric instability-Facial anomalies syndrome type 4', 'immunodeficiency-centromeric instability-Facial anomalies syndrome 4', 'ICF4']",0090011,616911,,C4310798,,,,,,,,
mondo:0014830,platelet-type bleeding disorder 20,"['bleeding disorder, platelet-type, 20', 'SLFN14 inherited bleeding disorder, platelet-type', 'BDPLT20', 'inherited bleeding disorder, platelet-type caused by mutation in SLFN14', 'autosomal dominant thrombocytopenia with platelet secretion defect']",0111055,616913,466806,C4310797,,,,,,,,
mondo:0014831,progeroid and marfanoid aspect-lipodystrophy syndrome,"['Marfan lipodystrophy syndrome', 'MFLS', 'Marfanoid-progeroid syndrome', 'Marfan-progeroid-lipodystrophy syndrome']",,616914,300382,C4310796,"['-0.1943', '0.2705', '0.253', '-0.2412', '0.1908', '-0.4604', '0.012314', '0.2761', '-0.2084', '-0.0499', '-0.1791', '-0.11505', '0.1759', '0.07324', '-0.3694', '0.1871', '0.4302', '0.01028', '-0.1968', '-0.4333', '-0.23', '-0.1548', '0.3374', '0.02086', '0.2524', '0.1445', '-0.00725', '-0.069', '0.414', '-0.0504', '0.3887', '0.02945', '0.5303', '0.3513', '0.1919', '-0.0908', '-0.205', '-0.0985', '-0.2305', '-0.4678', '0.2627', '-0.0901', '-0.3193', '-0.00934', '0.2742', '-0.0444', '0.1136', '0.5366', '0.02435', '0.04333', '-0.0607', '0.1246', '0.1434', '0.1504', '-0.256', '-0.2617', '-0.03894', '-0.3035', '-0.03848', '-0.0883', '0.431', '0.1442', '-0.3901', '0.09717', '0.0768', '0.01851', '0.2109', '0.03748', '-0.1181', '0.416', '-0.5044', '0.2207', '0.1688', '-0.12286', '-0.2355', '-0.1775', '0.2172', '-0.2305', '-0.2764', '-0.2332', '-0.00411', '-0.1522', '-0.09393', '0.271', '0.00329', '0.08325', '-0.1405', '0.313', '0.3408', '0.002346', '0.179', '0.3738', '0.2607', '0.0873', '0.2725', '-0.0782', '0.3752', '-0.0661', '0.2131', '0.3171']",,,,,,,
mondo:0014832,"intellectual disability, autosomal recessive 53","['intellectual disability, autosomal recessive type 53', 'congenital disorder of glycosylation due to PIGG deficiency', 'intellectual disability, autosomal recessive 53', 'GPIBD13', 'glycosylphosphatidylinositol biosynthesis defect 13', 'MRT53', 'mental retardation, autosomal recessive 53', 'PIGG-CDG', 'mental retardation, autosomal recessive type 53', 'intellectual developmental disorder, autosomal recessive 53']",,616917,488635,C4310794,,,,,,,,
mondo:0014833,heart and brain malformation syndrome,"['heart and brain malformation syndrome', 'HBMS']",,616920,,C4310793,,,,,,,,
mondo:0014835,"striatal degeneration, autosomal dominant 2","['striatal degeneration, autosomal dominant caused by mutation in PDE10A', 'striatal Degeneration, autosomal dominant type 2', 'PDE10A striatal degeneration, autosomal dominant', 'ADSD2', 'striatal Degeneration, autosomal dominant 2', 'striatal degeneration, autosomal dominant']",,616922,,C4310791,,,,,,,,
mondo:0014836,Charcot-Marie-Tooth disease axonal type 2CC,"['Charcot-Marie-Tooth disease, axonal, type 2CC', 'CMT2CC', 'Charcot-Marie-Tooth disease caused by mutation in NEFH', 'NEFH Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth neuropathy type 2CC', 'Charcot-Marie-Tooth neuropathy, type 2Cc', 'Charcot-Marie-Tooth disease, axonal, type 2cc']",0110180,616924,,C4310790,,,,,,,,
mondo:0014837,thrombocytopenia 6,"['hereditary thrombocytopenia with early-onset myelofibrosis', 'THC6', 'thrombocytopenia 6', 'thrombocytopenia type 6', 'thrombocytopenia, autosomal dominant, 6']",,616937,480851,C4310789,,,,,,,,
mondo:0014838,Coffin-Siris syndrome 5,"['COFFIN-SIRIS syndrome 5', 'Coffin-Siris syndrome 5', 'Coffin-Siris syndrome type 5', 'SMARCE1 Coffin-Siris syndrome', 'CSS5', 'Coffin-Siris syndrome caused by mutation in SMARCE1']",0112368,616938,,C4310788,,,,,,,,
mondo:0014839,"chorea, childhood-onset, with psychomotor retardation","['COCPMR', 'chorea, childhood-onset, with psychomotor retardation']",,616939,,C4310787,"['-0.03708', '0.0747', '0.01397', '-0.0372', '-0.000497', '-0.10364', '0.001449', '0.11005', '-0.07806', '-0.0508', '-0.02817', '0.005836', '0.0002033', '0.01034', '-0.00869', '-0.02397', '0.005123', '-0.03836', '-0.0542', '-0.148', '0.003664', '-0.02773', '0.05893', '-0.0337', '0.0425', '-0.01117', '-0.0077', '-0.004898', '-0.01778', '-0.02061', '0.06174', '0.00343', '0.095', '0.01209', '-0.003345', '-0.02167', '-0.02597', '-0.01726', '-0.02486', '-0.0508', '0.03842', '-0.0753', '0.0007496', '-0.009094', '-0.01394', '-0.0552', '-0.02354', '0.0545', '-0.00631', '0.01842', '-0.02129', '0.02618', '-0.006794', '-0.02724', '-0.00945', '-0.05035', '0.06537', '-0.0366', '-0.06183', '0.02095', '0.01804', '0.012924', '0.02081', '0.014175', '0.0128', '-3.654e-05', '0.0791', '0.0812', '-0.0887', '0.06525', '-0.05807', '-0.001533', '0.0143', '-0.0411', '0.0255', '0.04343', '0.03348', '-0.01845', '-0.04465', '-0.0297', '0.0145', '-0.003479', '-0.01346', '0.08234', '-0.007416', '0.0204', '0.00746', '0.06058', '0.1012', '0.015465', '0.05447', '0.08527', '-0.005947', '0.02228', '0.10974', '0.04364', '0.05057', '-0.05405', '0.04785', '0.03687']",,,,,,,
mondo:0014840,"agammaglobulinemia 8, autosomal dominant","['autosomal agammaglobulinemia caused by mutation in TCF3', 'TCF3 autosomal agammaglobulinemia', 'AGM8', 'agammaglobulinemia 8, autosomal dominant', 'agammaglobulinemia, autosomal dominant, due to TCF3 defect']",0081140,616941,,C4310786,,,,,,,,
mondo:0014841,"trichothiodystrophy 6, nonphotosensitive","['nonphotosensitive trichothiodystrophy caused by mutation in GTF2E2', 'TTD6', 'trichothiodystrophy 6, nonphotosensitive', 'GTF2E2 nonphotosensitive trichothiodystrophy']",0111872,616943,,C4310785,,,,,,,,
mondo:0014842,"intellectual disability, autosomal dominant 41","['autosomal dominant intellectual disability 41', 'intellectual disability, autosomal dominant 41', 'mental retardation, autosomal dominant 41', 'TBL1XR1 autosomal dominant non-syndromic intellectual disability', 'autosomal dominant non-syndromic intellectual disability 41', 'autosomal dominant mental retardation 41', 'MRD41', 'intellectual disability, autosomal dominant type 41', 'autosomal dominant non-syndromic intellectual disability caused by mutation in TBL1XR1', 'mental retardation, autosomal dominant type 41']",0070071,616944,,C4310784,"['-0.04065', '0.10754', '0.0534', '-0.11224', '0.05225', '-0.1705', '0.004585', '0.143', '-0.10785', '-0.10535', '-0.05603', '-0.002897', '0.014244', '-0.03983', '0.01121', '-0.01195', '-0.01836', '-0.05588', '-0.05347', '-0.2426', '-0.03317', '0.02081', '0.0369', '-0.03403', '0.05496', '-0.00948', '-0.0147', '-0.01881', '0.01326', '-0.1002', '0.07697', '-0.03284', '0.1565', '0.05084', '0.0256', '-0.05203', '-0.0365', '-0.08966', '-0.0256', '-0.1122', '0.07605', '-0.1326', '0.04544', '-0.0335', '-0.01449', '-0.176', '-0.04993', '0.0782', '0.01915', '0.01947', '0.014', '0.005424', '-0.00945', '-0.05728', '-0.03857', '-0.05978', '0.10645', '-0.0245', '-0.12445', '0.04727', '0.083', '0.011406', '0.02498', '0.01272', '-0.005047', '0.02606', '0.0959', '0.09985', '-0.1042', '0.1099', '-0.10547', '-0.02328', '0.01569', '-0.11456', '0.09436', '0.05566', '0.0409', '-0.03029', '-0.0936', '-0.04883', '-0.02737', '-0.005962', '-0.0324', '0.155', '0.01825', '0.0701', '0.04434', '0.1174', '0.11053', '0.12', '0.04935', '0.139', '0.006264', '0.02354', '0.2673', '0.0776', '0.1273', '-0.147', '0.05368', '0.0847']",,,,,,,
mondo:0014843,premature ovarian failure 11,"['primary ovarian failure caused by mutation in ERCC6', 'premature ovarian failure type 11', 'ERCC6 primary ovarian failure', 'premature ovarian failure 11', 'POF11']",0080869,616946,,C4310783,,,,,,,,
mondo:0017773,hypoalphalipoproteinemia,,,,31153,C0473527,,C84774,,D052456,,,10065156,
mondo:0017774,hypobetalipoproteinemia,['hypo-beta-lipoproteinemia'],1390,,31154,C0020597,"['0.296', '0.425', '-0.07764', '-0.572', '0.3684', '-0.1444', '-0.523', '0.605', '-0.3977', '-0.1103', '-0.3738', '-0.2229', '0.1826', '0.2023', '-0.3193', '-0.5054', '0.4087', '0.08954', '-0.03445', '-0.3735', '0.1266', '-0.726', '0.619', '0.361', '0.2238', '0.4927', '0.01688', '-0.2411', '-0.32', '-0.74', '0.624', '-0.0677', '0.2666', '0.3696', '-0.4302', '0.0969', '-0.5894', '0.0552', '-0.1339', '-0.4922', '-0.2003', '-0.663', '0.0543', '-0.2238', '0.0685', '-0.7188', '0.1669', '0.5503', '-0.00411', '-0.2559', '0.3315', '0.09216', '0.003683', '-0.3787', '-0.1997', '-0.4814', '0.3237', '-0.414', '-0.616', '0.518', '0.00965', '0.0744', '0.2937', '-0.5835', '0.01408', '0.5522', '-0.2705', '0.1006', '0.1086', '-0.2756', '0.158', '-0.0409', '0.5244', '-0.4392', '0.8164', '0.275', '0.04407', '-0.0427', '0.126', '0.1764', '-0.4438', '-0.05045', '-0.4797', '-0.1674', '0.2206', '0.1763', '0.005272', '-0.833', '0.361', '0.2391', '0.5215', '-0.1698', '-0.11', '-0.2402', '0.2367', '0.559', '0.148', '-0.9624', '-0.2756', '0.04803']",,,D006995,,,,
mondo:0017775,melioidosis,"['Burkholderia pseudomallei infection', 'pseudoglanders', 'acute and fulminating melioidosis', 'Whitmore^s disease', 'Burkholderia pseudomallei caused disease or disorder', 'subacute and chronic melioidosis', 'B pseudomallei infection', 'Whitmore disease', 'Nightcliff gardener^s disease']",5052,,31202,C0348971,,C128336,,D008554,025,,10069748,
mondo:0017776,nocardiosis,"['Nocardia caused disease or disorder', 'lung nocardiosis', 'Nocardia infectious disease', 'Nocardia infection']",2312,,31204,,,C171147,0007397,D009617,,A43,10029444,
mondo:0017778,lamellar ichthyosis,"['congenital lamellar ichthyosis', 'classic lamellar ichthyosis', 'LI']",,,313,,,C84805,,,,,10023686,
mondo:0017779,alpha-N-acetylgalactosaminidase deficiency,"['alpha-N-acetylgalactosaminidase activity disease', 'NAGA deficiency', 'disorder of alpha-N-acetylgalactosaminidase activity', 'Schindler disease']",0112317,,3137,,"['-0.0182', '-0.4243', '0.1821', '0.02556', '0.1371', '-0.6323', '0.6304', '0.0864', '-0.6406', '-0.11365', '-0.526', '-0.2146', '-0.10834', '0.07306', '0.5044', '0.1539', '0.01107', '-0.1182', '-0.07104', '-0.5884', '0.04272', '-0.2295', '0.2416', '-0.2957', '-1.012', '-0.04645', '-0.0735', '-0.3398', '-0.1908', '-0.61', '0.585', '0.0224', '0.3396', '0.1274', '-0.0232', '-0.516', '0.4285', '-0.4346', '-0.1698', '-0.1005', '0.2903', '-0.815', '0.3643', '0.01682', '0.2917', '-0.3403', '0.2598', '0.05026', '-0.371', '0.4666', '-0.491', '-0.1989', '0.255', '0.007744', '0.1925', '0.06287', '-0.2908', '-0.3638', '-0.2019', '0.0943', '-0.1725', '-0.06082', '0.8535', '0.07043', '0.2098', '-0.09064', '0.01944', '-0.2725', '-0.642', '-0.01732', '-0.4583', '0.001718', '-0.3425', '-0.03763', '0.793', '0.727', '-0.277', '-0.155', '-0.2483', '-0.1809', '0.0598', '0.196', '-0.3027', '0.9053', '0.2242', '0.5293', '0.4866', '0.293', '0.8003', '-0.297', '0.637', '0.1971', '0.01302', '0.0754', '0.04135', '0.4446', '-0.01525', '-0.138', '0.3113', '-0.02992']",,,,277.89,,,
mondo:0017780,20p13 microdeletion syndrome,"['monosomy 20p13', 'Del(20)(p13)', '20p subtelomeric deletion syndrome']",,,313781,CN203720,,,,,,,,
mondo:0017781,12p12.1 microdeletion syndrome,"['Del(12)(p12.1)', 'monosomy 12p12.1']",,,313884,CN203731,,,,,,,,
mondo:0017782,developmental and speech delay due to SOX5 deficiency,,,,313892,,"['-0.4612', '0.1372', '0.821', '-0.3206', '-0.0599', '0.04874', '0.2246', '0.3955', '-0.3945', '-0.1085', '-0.2092', '-0.12256', '-0.03613', '-0.1307', '-0.04764', '0.10077', '0.1982', '-0.199', '-0.2866', '-0.56', '0.0831', '0.05704', '0.0814', '0.03558', '0.1671', '-0.035', '-0.1251', '-0.02176', '0.295', '-0.1995', '0.0006485', '0.003145', '0.5503', '0.3691', '0.1403', '-0.2708', '-0.06757', '-0.1062', '-0.175', '-0.704', '0.1257', '-0.0654', '-0.1802', '-0.005257', '-0.0383', '-0.1385', '0.3628', '0.3523', '-0.07306', '0.009415', '-0.3838', '0.0524', '-0.197', '0.01422', '-0.1599', '-0.116', '-0.08966', '-0.0979', '-0.10016', '0.1416', '0.0803', '-0.07477', '-0.2157', '0.10046', '-0.1107', '-0.08765', '0.11896', '0.404', '-0.173', '0.2886', '-0.3489', '0.367', '0.05353', '-0.0777', '-0.2117', '0.04855', '0.545', '-0.2686', '-0.4094', '-0.129', '0.03008', '-0.1164', '-0.0623', '0.684', '0.08185', '0.2169', '-0.05765', '0.4348', '0.594', '0.556', '0.1528', '0.588', '-0.09015', '0.04608', '0.6304', '0.2054', '0.357', '-0.03098', '0.472', '0.4045']",,,,,,,
mondo:0017783,congenital pancreatic cyst,"['true congenital pancreatic cyst', 'neonatal congenital pancreatic cyst']",,,313906,,,,,,,Q45.2,,
mondo:0017784,Epstein-Barr virus-associated gastric carcinoma,"['EBV-associated gastric carcinoma', 'EBVaGC']",,,313920,CN203734,,,,,,,,
mondo:0017785,PENS syndrome,['papular epidermal nevi with skyline basal cell layers syndrome'],,,313936,CN203735,,,,,,,,
mondo:0017786,2q23.1 microduplication syndrome,"['trisomy 2q23.1', 'dup(2)(q23.1)']",,,313947,CN203736,,,,,,,,
mondo:0017787,erythroderma desquamativum,"['generalized erythroderma, diarrhea, and failure to thrive', 'Leiner-Moussous desquamative erythroderma', 'erythroderma desquamativum of infancy', 'Leiner disease', 'generalised erythroderma, diarrhea, and failure to thrive', 'erythroderma desquamativa of Leiner']",,,314,CN203737,,,,C535512,,,,
mondo:0017788,contractures - webbed neck - micrognathia - hypoplastic nipples syndrome,['Dinno syndrome'],,,314002,CN203738,,,,,,,,
mondo:0017789,idiopathic linear interstitial keratitis,,,,314017,,,,,,,,,
mondo:0017790,gastric adenocarcinoma and proximal polyposis of the stomach,"['polyposis, gastric', 'polyposis, gastric, Dos Santos and de Magalhaes 1980', 'GAPPS', 'fundic gland polyposis', 'familial fundic gland polyposis with gastric cancer']",,619182,314022,CN203740,"['0.0971', '0.1447', '-0.2267', '-0.3162', '0.06573', '-0.2161', '0.1433', '0.2817', '-0.2465', '0.2954', '0.1042', '0.2124', '0.0946', '-0.401', '-0.2522', '-0.3489', '0.01531', '-0.06647', '0.257', '-0.4', '-0.1255', '-0.2333', '0.3389', '-0.4316', '0.5195', '0.02477', '0.068', '-0.10406', '0.3198', '-0.4087', '0.4458', '-0.3235', '0.1946', '-0.09717', '0.2072', '-0.0689', '-0.4749', '-0.19', '0.001509', '-0.1351', '0.187', '-0.265', '0.1914', '-0.2422', '0.1464', '0.01469', '-0.2472', '0.2617', '0.1003', '0.0627', '-0.04086', '0.0735', '-0.2253', '-0.1542', '-0.307', '-0.1936', '-0.09', '-0.1598', '-0.5967', '-0.0953', '0.6885', '0.2957', '0.10754', '-0.06464', '0.09534', '0.3882', '0.5186', '0.1173', '-0.2056', '0.565', '0.01958', '0.0709', '0.1294', '0.02658', '-0.02367', '-0.2175', '-0.11383', '0.0773', '-0.1266', '-0.3062', '-0.1349', '0.1941', '-0.02681', '0.07947', '-0.3796', '-0.3916', '-0.007034', '0.1797', '0.0913', '-0.3784', '0.1488', '0.1534', '0.1222', '-0.0431', '0.4514', '-0.2345', '0.446', '-0.591', '-0.5566', '-0.06226']",C172989,,,,,,
mondo:0017791,high bone mass osteogenesis imperfecta,['high bone mass OI'],,,314029,CN203741,,,,,,Q78.0,,
mondo:0017792,7p22.1 microduplication syndrome,"['trisomy 7p22.1', 'dup(7)(p22.1)']",,,314034,CN203742,,,,,,,,
mondo:0017793,marfanoid habitus-inguinal hernia-advanced bone age syndrome,,,,314041,CN203743,,,,,,,,
mondo:0017794,Xq12-q13.3 duplication syndrome,['dup(X)(q12-q13.3)'],,,314389,CN203749,,,,,,,,
mondo:0017795,ameloblastoma,"['aot', 'adamantinoma', 'adenomatoid odontogenic tumour', 'Adenoameloblastoma', 'ameloblastoma of jaw', 'adenomatoid odontogenic tumor', 'ameloblastoma']",0050894,,314419,C0563212,,C4313,,D000564,,,10066796,
mondo:0017798,Spigelian hernia-cryptorchidism syndrome,,,,314432,CN203757,,,,,,,,
mondo:0017799,Meigs syndrome,"['Demons-Meigs syndrome', 'Meigs^ syndrome']",,,314451,C0025184,,C3223,,D008539,629.89,,10027139,
mondo:0017800,pseudo-Meigs syndrome,['pseudo-Demons-Meigs syndrome'],,,314459,CN203759,,,,,,,,
mondo:0017801,atypical Meigs syndrome,"['atypical Demons-Meigs syndrome', 'incomplete Meigs syndrome']",,,314466,CN203760,,,,,,,,
mondo:0017802,ovarian fibrothecoma,,,,314478,CN203762,,,,,,,,
mondo:0017803,primary progressive apraxia of speech,['PPAOS'],,,314566,CN203766,,,,,,,,
mondo:0017804,autosomal recessive leukoencephalopathy-ischemic stroke-retinitis pigmentosa syndrome,,,,314572,CN203767,,,,,,,,
mondo:0017805,intellectual disability-hypotonia-brachycephaly-pyloric stenosis-cryptorchidism syndrome,,,,314575,CN203768,,,,,,,,
mondo:0017806,15q overgrowth syndrome,['15q26 overgrowth syndrome'],,,314585,CN203769,,,,,,,,
mondo:0017807,growing teratoma syndrome,['GTS'],,,314613,CN203773,,C118370,,,,,,
mondo:0017808,duplication of the pituitary gland,"['hypophyseal duplication', 'DPG-plus syndrome', 'Duplication of the pituitary gland-plus syndrome']",,,314621,CN203774,,,,,,,,
mondo:0017809,parkinsonism due to ATP13A2 deficiency,['CLN12 disease'],,,314632,CN203776,"['-0.5786', '0.3892', '0.2024', '-0.1249', '-0.1603', '-0.4456', '-0.01264', '-0.10693', '-0.5337', '0.0694', '-0.3496', '0.05304', '-0.164', '-0.3674', '0.435', '-0.2031', '0.1705', '-0.2192', '-0.1974', '-0.499', '0.3281', '-0.2974', '0.00999', '-0.09344', '-0.0462', '0.02402', '0.07825', '-0.2429', '-0.5786', '0.0742', '0.0166', '0.261', '0.3984', '-0.004192', '0.3127', '0.01904', '-0.0353', '-0.148', '-0.2495', '-0.3447', '0.1665', '-0.565', '0.02505', '0.3513', '-0.03168', '-0.509', '-0.06207', '0.3206', '0.00642', '0.0882', '0.1594', '0.3508', '-0.2498', '-0.0645', '0.1009', '-0.5635', '0.5474', '-0.281', '-0.5146', '0.2024', '0.2502', '0.0481', '-0.1101', '0.10895', '-0.3462', '-0.0821', '0.5454', '0.1995', '-0.2156', '0.2659', '-0.1521', '-0.10504', '0.01412', '-0.2578', '0.08075', '0.0344', '-0.02344', '0.2297', '-0.0957', '-0.0741', '0.1913', '-0.5527', '0.0812', '0.6865', '-0.1182', '-0.1337', '0.0557', '0.2476', '0.3567', '-0.07367', '0.4917', '0.2135', '0.0722', '0.08057', '0.2054', '0.3086', '0.3462', '0.1892', '0.17', '0.2593']",,,,,,,
mondo:0017810,variant ABeta2M amyloidosis,['autosomal dominant beta2-microglobulinic amyloidosis'],0080929,,314652,CN203779,,,,,,,,
mondo:0017811,severe neonatal hypotonia-seizures-encephalopathy syndrome due to 5q31.3 microdeletion,"['Del(5)(q31.3)', 'monosomy 5q31.3', '5q31.3 microdeletion syndrome']",,,314655,CN203780,,,,,,,,
mondo:0017812,segmental progressive overgrowth syndrome with fibroadipose hyperplasia,,,,314662,CN203781,,,,,,,,
mondo:0017813,van Maldergem syndrome,"['Van Maldergem syndrome', 'cerebro-facio-articular syndrome', 'cerebro-facio-articular syndrome of Van Maldergem', 'Van Maldergem Wetzburger Verloes syndrome']",0060238,,314679,CN203783,"['-0.2208', '-0.02167', '0.1582', '-0.438', '0.1309', '-0.518', '-0.1414', '0.3796', '-0.6377', '-0.1718', '-0.2546', '-0.2527', '-0.286', '0.1531', '-0.2277', '0.1287', '0.1515', '0.07275', '-0.2483', '-0.6733', '0.1335', '-0.04504', '0.5767', '-0.2898', '0.214', '-0.02444', '0.02847', '-0.03378', '0.5073', '-0.2136', '0.01306', '-0.255', '0.4856', '0.285', '0.3535', '-0.2856', '-0.2578', '-0.3564', '-0.2021', '-0.3545', '0.03543', '-0.4937', '-0.1196', '0.1525', '-0.04343', '-0.2756', '-0.1437', '0.2595', '-0.0504', '0.04227', '-0.4255', '0.2388', '0.0546', '-0.1293', '-0.4841', '-0.1438', '0.2177', '-0.06366', '0.1526', '-0.0813', '0.4048', '0.2256', '-0.665', '0.2131', '-0.03632', '-0.358', '0.2406', '0.603', '0.02539', '0.1239', '-0.574', '0.2705', '-0.1987', '-0.06836', '-0.5166', '-0.552', '0.4226', '-0.0498', '-0.491', '-0.275', '-0.0809', '-0.05185', '0.1274', '0.606', '-0.1775', '0.3503', '-0.07904', '0.523', '0.1805', '0.0004742', '0.3264', '0.6567', '0.3318', '0.09503', '0.574', '0.2299', '0.5596', '-0.1766', '0.746', '0.2744']",,,,,,,
mondo:0017814,primary bone lymphoma,"['lymphoma of bone', 'bone lymphoma', 'primary lymphoma of bone', 'lymphoma of the bone', 'primary lymphoma of the bone', 'lymphoma of bone tissue', 'bone tissue lymphoma']",6759,,314684,C1332582,,C6620,,,,,,
mondo:0017815,acquired porencephaly,['acquired porencephaly'],,,314697,C0151860,,,,,,,,
mondo:0017816,primary systemic amyloidosis,"['systemic Immunoglobulin Light chain amyloidosis', 'systemic AL amyloidosis', 'systemic amyloidosis']",,,314701,C0281479,,C8299,,,,,,
mondo:0017817,primary localized amyloidosis,"['localized AL amyloidosis', 'localised AL amyloidosis']",,,314709,,"['0.318', '-0.6436', '-0.4011', '0.1619', '0.4524', '-0.177', '-0.6177', '0.1615', '-1.437', '0.0939', '-0.01146', '0.1205', '-1.224', '0.3176', '-0.982', '0.02196', '0.01843', '-0.4897', '0.04227', '-0.6562', '0.426', '-0.2145', '0.895', '-0.3428', '0.3096', '0.5005', '-0.648', '-0.2673', '0.3933', '0.2489', '0.2133', '-0.1805', '0.9727', '-0.85', '0.2751', '-0.8447', '-0.4482', '0.4492', '0.2944', '-0.07184', '0.2263', '-0.234', '-0.06323', '0.09174', '0.3186', '-0.7407', '-0.544', '0.2976', '0.4067', '1.181', '0.02582', '0.46', '0.311', '-0.3818', '-0.533', '-0.0678', '0.3906', '-0.0916', '-0.527', '-0.829', '-0.381', '0.4817', '0.3726', '-0.887', '0.06226', '-0.2335', '0.604', '1.248', '-0.407', '0.3782', '-0.2998', '0.4907', '-0.703', '-0.005882', '0.352', '0.676', '-0.483', '1.225', '-0.3035', '-0.9053', '-0.393', '-0.1868', '-0.04327', '0.08606', '-0.1179', '-0.681', '0.007866', '-0.2827', '0.4976', '-0.1818', '0.501', '-0.2886', '-0.398', '-0.6094', '0.7793', '0.601', '-0.675', '-0.2532', '0.10443', '0.2651']",,,,,,,
mondo:0017818,lethal arteriopathy syndrome due to fibulin-4 deficiency,,,,314718,CN203788,,,,,,,,
mondo:0017819,atypical dentin dysplasia due to SMOC2 deficiency,['dentin dysplasia type 1 with microdontia and shape anomalies'],,,314721,CN203789,"['-0.237', '-0.002165', '0.3564', '-0.2185', '0.1718', '0.02501', '0.1171', '0.1913', '-0.0333', '0.000762', '-0.1587', '-0.3213', '-0.1505', '-0.02835', '-0.3572', '-0.02794', '0.185', '-0.388', '-0.2231', '-0.6094', '-0.12305', '0.1487', '0.404', '-0.04388', '0.1454', '0.006756', '-0.3242', '0.04642', '0.2028', '-0.252', '0.16', '0.2085', '0.138', '0.1506', '0.1625', '-0.0576', '0.0665', '-0.296', '0.08124', '-0.673', '0.2996', '-0.1161', '-0.0956', '-0.2415', '-0.2522', '-0.332', '0.08966', '0.2195', '0.2075', '-0.02579', '0.1214', '0.05725', '0.1823', '0.06433', '-0.4126', '-0.2815', '0.1808', '-0.2668', '-0.2222', '-0.0983', '0.1566', '0.1177', '-0.3345', '1.305e-05', '0.1837', '-0.01361', '0.3948', '0.236', '0.02374', '0.267', '-0.3203', '0.10913', '0.2329', '-0.2554', '-0.0189', '-0.001236', '0.0818', '-0.2133', '-0.014366', '-0.12225', '-0.04828', '0.0337', '0.05002', '0.221', '0.05847', '-0.05447', '-0.08057', '0.1096', '0.3135', '-0.03946', '-0.19', '0.32', '0.1335', '0.306', '0.483', '0.05563', '0.3396', '-0.2725', '0.31', '0.0981']",,,,,,,
mondo:0017822,mixed functioning pituitary adenoma,['mixed secreting pituitary adenoma'],,,314759,C0346305,,,,,,,,
mondo:0017823,somatomammotropinoma,"['GH and PRL cosecreting pituitary adenoma', 'Somatolactotropinoma', 'Growth hormone and prolactin cosecreting pituitary adenoma', 'Somatoprolactinoma']",,,314769,CN203793,,,,,,D35.2,,
mondo:0017824,familial isolated pituitary adenoma,['FIPA'],,,314777,CN244420,,,,,,D35.2,,
mondo:0017825,silent pituitary adenoma,,,,314786,CN203795,,,,,,D35.2,,
mondo:0017826,null pituitary adenoma,,,,314790,CN203796,,,,,,D35.2,,
mondo:0017827,malignant peripheral nerve sheath tumor,"['malignant neoplasm of the peripheral nerve sheath', 'malignant tumour of peripheral nerve sheath', 'malignant neurofibroma', 'Malig. periph. nerve sheath tum.', 'malignant schwannoma', 'malignant neurilemmoma', 'malignant peripheral nerve sheath neoplasm', 'malignant neurilemoma', 'malignant peripheral nerve sheath tumor', 'malignant neoplasm of peripheral nerve sheath', 'malignant peripheral nerve sheath tumour [dup] (morphologic abnormality)', 'neurofibrosarcoma, malignant', 'MPNST', 'malignant peripheral nerve sheath tumor [dup] (morphologic abnormality)', 'malignant peripheral nerve sheath tumour (morphologic abnormality)', 'malignant peripheral nerve sheath tumor (morphologic abnormality)', 'neurogenic sarcoma', 'malignant tumor of peripheral nerve sheath', 'malignant tumour of the peripheral nerve sheath', 'malignant tumor of the peripheral nerve sheath', 'schwannoma, malignant', 'neurofibrosarcoma']",5940,,3148,C0751690,,C3798,,,171.9,,10029236,
mondo:0017828,primary renal tubular acidosis,,,,314822,,,,,,,,,
mondo:0017829,autosomal dominant proximal renal tubular acidosis,"['AD pRTA', 'proximal renal tubular acidosis, autosomal dominant']",,,314889,CN203801,,,,,,,,
mondo:0017830,severe Canavan disease,"['neonatal Canavan disease', 'infantile Canavan disease']",,,314911,CN203803,,,,,,,,
mondo:0017831,mild Canavan disease,['juvenile Canavan disease'],,,314918,,,,,,,,,
mondo:0017832,mycobacterium xenopi infection,"['Mycobacterium xenopi', 'Mycobacterium xenopi caused disease or disorder', 'M. xenopi']",,,314946,C0275715,,,,,,,,
mondo:0017833,primary hypereosinophilic syndrome,"['neoplastic hypereosinophilic syndrome', 'primary HES', 'clonal hypereosinophilic syndrome', 'HES-N', 'HES-M']",,,314950,CN203808,,,,,,,,
mondo:0017834,secondary hypereosinophilic syndrome,"['reactive hypereosinophilic syndrome', 'secondary HES', 'HES-R']",,,314962,CN203809,,,,,,,,
mondo:0017835,lymphocytic hypereosinophilic syndrome,"['lymphoid HES', 'lymphocytic variant HES', 'HES-L']",,,314970,CN203810,,,,,,,,
mondo:0017836,erythrokeratoderma en cocardes,"['Degos ^en cocarde^ erythrokeratoderma', 'Degos genodermatosis ""en cocardes""', 'erythrokeratoderma ^en cocardes^', 'erythrokeratoderma ""en cocardes""', 'Degos genodermatosis', 'erythrokeratoderma ^^en cocardes^^', 'Degos genodermatosis ^en cocardes^']",,,315,CN203813,,,,,447.8,,,
mondo:0017837,multiple sclerosis-ichthyosis-factor VIII deficiency syndrome,,,,3151,CN203814,,,,,,,,
mondo:0017838,sclerosteosis,"['cortical hyperostosis-syndactyly syndrome', 'cortical hyperostosis with syndactyly']",0060251,,3152,C0265301,"['-0.3613', '0.189', '0.297', '-0.10443', '-0.01431', '0.06085', '-0.02301', '0.2417', '-0.2593', '0.073', '-0.2072', '0.02551', '0.2134', '-0.11365', '-0.2104', '-0.3027', '0.1709', '0.1644', '-0.164', '-0.5527', '0.1608', '-0.2009', '0.2708', '-0.04605', '0.2135', '0.2742', '-0.1204', '-0.05472', '0.2039', '-0.01414', '-0.00438', '0.0995', '0.2842', '0.2482', '-0.01048', '0.04865', '0.07666', '-0.3064', '-0.01044', '-0.505', '-0.02815', '-0.2175', '0.1428', '-0.2423', '-0.0539', '-0.186', '0.006092', '0.1759', '0.2493', '-0.1896', '-0.0884', '0.03937', '0.06915', '-0.04816', '-0.473', '-0.4072', '-0.2285', '0.04004', '-0.1102', '-0.009476', '0.156', '-0.1522', '-0.223', '0.01567', '-0.3599', '-0.02304', '0.01551', '0.5117', '-0.4646', '0.3774', '-0.1678', '0.2634', '0.2766', '0.1464', '-0.2605', '-0.1549', '0.0957', '0.0988', '-0.2296', '-0.3801', '-0.362', '-0.2413', '-0.1282', '0.5303', '-0.137', '0.111', '0.1192', '0.293', '0.1871', '-0.2014', '-0.177', '0.1865', '0.05994', '-0.01092', '0.4065', '-0.02866', '0.707', '-0.0959', '0.1293', '0.2017']",C131133,,C537525,756.59,,,
mondo:0017839,"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, salt wasting form","['classic 21-OHD CAH, salt wasting form']",,,315306,,,,,,,,,
mondo:0017840,"classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency, simple virilizing form","['classic 21-OHD CAH, simple virilizing form']",,,315311,,,,,,,,,
mondo:0017842,Senior-Loken syndrome,"['SLSN', 'nephronophthisis with retinal dystrophy', 'Senior Loken syndrome', 'renal dysplasia retinal aplasia', 'renal dysplasia-retinal aplasia syndrome', 'renal-retinal syndrome', 'Loken Senior syndrome']",0050576,,3156,CN117960,"['-0.4639', '-0.09094', '-0.2766', '0.3914', '0.3933', '-0.5454', '-0.3262', '0.5405', '-0.2268', '-0.10144', '-0.4814', '-0.4314', '-0.1382', '0.383', '0.056', '-0.1315', '0.309', '0.01094', '0.3496', '-1.149', '-0.4546', '-0.01973', '0.1561', '0.3042', '0.05743', '-0.4275', '-0.03577', '0.04727', '-0.0163', '0.03937', '0.746', '-0.251', '-0.1056', '0.7017', '0.1508', '-0.00842', '-0.182', '-0.2935', '0.0673', '-0.0649', '-0.2412', '0.1515', '0.9214', '0.0715', '0.2913', '-0.2668', '-0.2937', '-0.3074', '-0.306', '-0.2534', '0.1407', '0.537', '0.3496', '-0.999', '0.0918', '-0.3481', '0.4146', '0.1472', '-1.096', '-0.3186', '0.3052', '0.07526', '0.3064', '-0.1357', '0.353', '-0.613', '0.3882', '0.135', '-0.2637', '-0.1814', '-0.7007', '-0.935', '0.124', '0.3645', '0.669', '-0.902', '0.4558', '-0.03824', '-0.005756', '0.1327', '0.3713', '0.1781', '-0.0779', '0.832', '0.2212', '0.2408', '0.3486', '-0.1357', '0.2676', '0.642', '0.6074', '0.323', '-0.672', '0.2617', '0.58', '0.0743', '0.2024', '-0.3975', '-0.506', '0.506']",C168588,,C537580,,,,
mondo:0017843,congenital pulmonary sequestration,"['sequestered lobe (pulmonary sequestration)', 'bronchopulmonary sequestration', 'pulmonary sequestration', 'congenital sequestration of lung', 'congenital bronchopulmonary sequestration']",,,3161,C4020703,,C97124,,D001998,,,,
mondo:0017844,Sezary syndrome,"['cutaneous T-cell lymphoma/Sezary syndrome', 'Sezary^s disease', 'Sezary disease', 'Sezary syndrome', 'Sezary^s lymphoma', 'CTCL / Sezary syndrome', 'Sezary lymphoma', 'SS', 'Sézary lymphoma', 'SC)zary syndrome', 'Sézary syndrome']",8541,,3162,C0036920,,C3366,1000785,D012751,202.2,,10040500,
mondo:0017845,spastic ataxia,['SPAX'],0050952,,316226,C1849156,,,,C564815,,G11.4,,
mondo:0017846,autosomal dominant spastic ataxia,"['spastic ataxia, autosomal dominant', 'AD-SPAX']",,,316235,CN229111,,,,,,G11.4,,
mondo:0017847,autosomal recessive spastic ataxia,"['spastic ataxia, autosomal recessive', 'AR-SPAX']",,,316240,CN229112,"['-0.0479', '-0.1962', '-0.05334', '0.1898', '-0.1148', '-1.026', '0.2578', '-0.03183', '-0.552', '-0.8213', '0.1763', '0.1469', '-0.4172', '0.3518', '0.3757', '-0.3552', '-0.3032', '-0.3225', '0.0907', '-1.034', '-0.08673', '-0.392', '0.1787', '-0.7017', '0.4932', '-0.601', '-0.3118', '0.1348', '0.001886', '-0.817', '0.0402', '0.2654', '-0.5356', '-0.1958', '0.3613', '0.1987', '-0.194', '0.1503', '0.5073', '0.2448', '0.26', '0.276', '-0.4216', '0.4033', '0.6167', '-0.7397', '0.1726', '0.5103', '0.5093', '0.008606', '-0.0624', '0.1786', '-0.1311', '-0.217', '-0.0652', '-0.874', '0.4412', '0.6626', '-0.2323', '0.312', '-0.612', '0.2446', '0.2123', '-0.03598', '-0.4138', '0.6826', '0.37', '0.613', '-0.625', '0.477', '1.086', '0.3667', '-0.1187', '-0.8853', '0.851', '0.3154', '0.2734', '0.3835', '0.2605', '0.5957', '-0.368', '-0.886', '0.1779', '0.7603', '-0.2717', '-0.666', '0.2505', '-0.1362', '0.3918', '0.446', '0.317', '0.4963', '0.01257', '0.1393', '0.97', '1.132', '0.2174', '0.351', '-0.487', '0.0611']",,,,,,,
mondo:0017849,Siegler-Brewer-Carey syndrome,"['Siegler Brewer Carey syndrome', 'fatal multisystem syndrome involving the eyes, ears, lungs, intestines, and kidneys']",,,3167,C2931473,,,,C537335,,,,
mondo:0017850,sirenomelia,"['mermaid malformation', 'sirenomelia sequence', 'Sirenomelus', 'symmelia', 'mermaid syndrome', 'Fused legs and feet']",,,3169,C0037205,"['-0.3406', '-0.3843', '0.0969', '-0.2532', '-0.1592', '-0.4602', '-0.0654', '0.4407', '-0.4246', '-0.3723', '-0.509', '-0.4033', '-0.1329', '0.2355', '-0.3809', '-0.1964', '0.0971', '-0.2396', '-0.219', '-0.5537', '0.06586', '0.081', '0.6', '-0.2769', '-0.03177', '-0.2695', '-0.05856', '0.4707', '0.2803', '-0.145', '0.1646', '-0.02228', '0.2048', '0.3438', '0.4067', '-0.05252', '-0.1262', '-0.0722', '-0.0982', '0.1316', '0.073', '0.207', '0.118', '-0.04346', '-0.1837', '-0.354', '-0.0238', '0.2084', '0.1628', '0.3699', '-0.187', '-0.002188', '-0.1093', '-0.0347', '-0.617', '-0.0631', '-0.3374', '-0.309', '0.0282', '0.1685', '0.09814', '0.2588', '-0.012535', '0.265', '-0.3962', '0.3037', '0.444', '0.555', '-0.3398', '0.356', '0.003063', '0.1799', '-0.098', '0.0353', '-0.09174', '-0.0533', '0.3735', '-0.0567', '-0.525', '-0.3499', '-0.444', '0.0573', '0.662', '0.1824', '-0.10004', '-0.1433', '0.1475', '0.05948', '-0.0763', '-0.2603', '0.2451', '0.2079', '0.3865', '-0.00971', '0.3987', '-0.05994', '0.5786', '-0.266', '0.10297', '0.4873']",C118455,,,,,10049216,
mondo:0017851,erythrokeratodermia variabilis,"['Darier-Gottron disease', 'erythrokeratodermia variabilis ET progressiva', 'keratosis palmoplantaris transgrediens et progrediens', 'erythrokeratodermia, progressive symmetric', 'EKV', 'erythrokeratodermia variabilis', 'erythrokeratodermia variabilis, Mendes da Costa type', 'progressive symmetric erythrokeratodermia, Gottron type', 'erythrokeratodermia figurata, congenital familial, in plaques', 'erythrokeratodermia variabilis with erythema gyratum repens', 'erythrokeratodermia progressiva symmetrica', 'Greither^s disease', 'keratoderma palmoplantaris transgrediens', 'keratosis extremitatum hereditaria progrediens', 'keratosis palmoplantaris transgrediens Et progrediens', 'EKVP', 'erythrokeratodermia Figurata, congenital familial, in plaques', 'erythrokeratodermia Figurata variabilis', 'progressive symmetric erythrokeratodermia', 'erythrokeratodermia variabilis with erythema Gyratum Repens']",0050467,,317,C0265961,"['-0.1177', '0.0845', '-0.01231', '-0.08875', '0.1364', '-0.3787', '-0.0377', '0.05228', '-0.0979', '-0.1306', '-0.09174', '-0.0328', '-0.1332', '-0.1345', '0.04904', '0.07306', '0.1511', '-0.1544', '-0.0765', '-0.3672', '-0.03638', '-0.0489', '0.0929', '-0.03806', '0.0837', '0.0401', '-0.0944', '-0.0824', '-0.1517', '-0.3345', '0.1243', '0.000495', '0.04922', '0.1814', '0.1265', '-0.1732', '-0.07965', '-0.09796', '-0.0259', '-0.1643', '0.01782', '-0.416', '0.08575', '-0.0657', '0.02568', '-0.2478', '-0.2125', '0.1149', '0.067', '-0.0642', '-0.1522', '-0.05975', '0.03232', '0.0802', '-0.02206', '-0.0977', '0.388', '-0.013885', '-0.3662', '0.0492', '0.0637', '0.0518', '-0.05368', '0.004475', '0.06183', '0.01524', '0.1554', '0.288', '-0.03378', '0.451', '-0.2373', '-0.1853', '0.06866', '0.1656', '0.0999', '0.217', '0.011665', '0.09937', '-0.09', '0.006134', '0.10736', '0.1316', '-0.01843', '0.1835', '-0.02194', '0.09595', '0.067', '0.4114', '0.04764', '0.02141', '0.1958', '0.1768', '-0.0687', '0.0359', '0.3918', '0.06', '0.3276', '-0.2607', '-0.06647', '0.0349']",C84696,,D056266,,,10049048,
mondo:0017852,infantile spasms-broad thumbs syndrome,"['Tsao-Ellingson syndrome', 'infantile spasms broad thumbs', 'Tsao Ellingson syndrome']",,,3173,CN203849,,,,,,,,
mondo:0017853,hypersensitivity pneumonitis,"['allergic interstitial pneumonitis', 'extrinsic allergic pneumonia hypersensitivity pneumonitis', 'exogen allergic alveolitis', 'alveolitis, extrinsic allergic', 'HP', 'hypersensitivity pneumonitis', 'allergic pneumonitis', 'extrinsic allergic alveolitis', 'alveolitis', 'allergic form of pneumonitis']",841,,31740,,,C34369,,D000542,495.9,J67.2,10001890,
mondo:0017855,T-B- severe combined immunodeficiency,['T-B- SCID'],,,317419,,,,,,,,,
mondo:0017856,X-linked spasticity-intellectual disability-epilepsy syndrome,,,,3175,CN203866,"['0.9355', '0.127', '-0.421', '-0.10944', '-0.4517', '-0.512', '0.783', '0.2869', '-0.545', '-0.445', '-0.0876', '-0.3445', '-0.4146', '0.3708', '0.1334', '-0.06366', '-0.3726', '-0.4746', '-0.609', '-0.6816', '-0.2074', '0.7495', '0.05716', '-0.493', '-0.1879', '0.04916', '-0.1002', '-0.1399', '-0.4397', '0.3726', '0.2734', '-0.6846', '0.396', '0.2617', '0.859', '0.3816', '-0.12195', '-0.02806', '-0.09186', '-0.5728', '-0.2013', '-0.4104', '0.05847', '-0.2361', '-0.646', '-0.6978', '-0.3342', '0.2451', '0.4844', '0.5894', '-0.2444', '0.1925', '0.05798', '-0.5845', '-0.0425', '-0.2979', '-0.05325', '0.005817', '-0.133', '0.3792', '-1.028', '0.5693', '0.9155', '-0.256', '-0.3792', '1.413', '-0.05798', '-0.02028', '-1.003', '0.7144', '1.025', '1.029', '-0.03888', '-0.4302', '-0.01305', '0.759', '0.9546', '0.461', '-0.4011', '0.2668', '-0.1678', '0.908', '0.4585', '0.4292', '0.5728', '0.1676', '0.02196', '0.721', '0.871', '0.4668', '0.0996', '0.02742', '-0.0944', '0.3652', '0.0586', '0.2186', '0.3215', '-0.4766', '0.1804', '0.2827']",,,,,,,
mondo:0017857,spina bifida-hypospadias syndrome,,,,3176,CN203872,,,,,,,,
mondo:0017858,acute erythroid leukemia,"['acute erythroleukemia M6a subtype', 'erythroblastic leukemia', 'acute myeloid leukemia M6', 'Di Guglielmo^s syndrome', 'leukemia, erythroid, malignant', 'erythroblastic leukaemia', 'acute erythroleukemia M6b subtype', 'acute erythroblastic leukaemia', 'Erythroleukemia', 'acute myeloid leukemia FAB-M6', 'AML-M6', 'FAB M6', 'acute myeloid leukaemia M6', 'acute erythroid leukemia', 'M6 acute myeloid leukaemia', 'AEL', 'Di Guglielmo syndrome', 'M6 acute myeloid leukemia', 'AML M6', 'acute myeloid leukaemia FAB-M6', 'acute erythroleukemia', 'acute erythroblastic leukemia']",0080780,,318,C0023440,,C8923,,D004915,207.00,,,
mondo:0017859,colchicine poisoning,,,,31824,CN203894,,,,,974.7,,,
mondo:0017860,methanol poisoning,,,,31825,CN203895,,,,,,,,
mondo:0017861,ethylene glycol poisoning,,,,31826,,,,,,982.8,,,
mondo:0017862,paraquat poisoning,,,,31827,CN227212,,,,,,,,
mondo:0017863,digitalis poisoning,,,,31828,CN203897,,,,,,,,
mondo:0017864,congenital pulmonary veins atresia or stenosis,"['pulmonary vein stenosis', 'pulmonary veins stenosis']",,,3188,C0340756,,,,,,,,
mondo:0017865,congenital pulmonary valve stenosis,"['valvate pulmonary stenosis', 'heart valve pulmonary stenosis', 'valvular pulmonary stenosis', 'valvar pulmonary stenosis']",,,3189,,,,,D011666,,Q22.1,10037451,
mondo:0017866,subpulmonary stenosis,,,,3190,C3165028,,,,,,,,
mondo:0017867,distal 17p13.1 microdeletion syndrome,['distal del(17)(p13.1)'],,,319171,CN203914,,,,,,,,
mondo:0017868,diencephalic-mesencephalic junction dysplasia,['diencephalic-mesencephalic junction dysplasia syndrome'],,,319192,,"['-0.3108', '0.2084', '0.299', '-0.3606', '-0.04117', '-0.149', '-0.03503', '0.4404', '-0.5615', '-0.0929', '-0.3647', '-0.3596', '-0.0626', '-0.5645', '0.0992', '-0.0472', '0.1055', '-0.2338', '-0.04187', '-0.553', '0.3152', '0.2156', '0.2559', '-0.0663', '0.1606', '-0.06137', '-0.04633', '0.02388', '0.2742', '-0.1033', '0.1799', '-0.152', '0.489', '0.04468', '0.2673', '0.1813', '-0.1578', '-0.12067', '-0.1199', '-0.3303', '0.2222', '-0.2391', '-0.126', '-0.02637', '-0.1261', '-0.2637', '-0.0361', '0.563', '-0.2905', '-0.2483', '0.01371', '0.2747', '-0.3958', '-0.01548', '-0.3516', '-0.1919', '0.04398', '-0.1532', '-0.1621', '0.3843', '0.1486', '0.1663', '-0.2213', '0.1284', '-0.3723', '-0.2048', '0.3542', '0.377', '-0.2568', '0.5913', '-0.2339', '0.4543', '0.09045', '-0.2556', '-0.3633', '0.006855', '0.2622', '-0.3254', '-0.05765', '-0.08527', '0.04312', '0.1818', '-0.05493', '0.5537', '-0.0677', '-0.0778', '-0.08734', '0.4854', '0.1532', '0.1802', '-0.09143', '0.10565', '0.1274', '0.323', '0.5957', '-0.004982', '0.4932', '-0.0713', '0.4153', '0.1962']",,,,,,,
mondo:0017869,chondroectodermal dysplasia with night blindness,,,,319195,,,,,,,,,
mondo:0017870,supravalvular pulmonary stenosis,['pulmonary supravalvular stenosis'],,,3192,,,,,,,,,
mondo:0017871,bilateral massive adrenal hemorrhage,"['BMAH', 'bilateral adrenal haemorrhage', 'bilateral adrenal hemorrhage']",,,319205,CN203920,,,,,,,,
mondo:0017872,Lujo hemorrhagic fever,['Zambian hemorrhagic fever'],0050202,,319213,CN203921,,,,,,,,
mondo:0017874,Argentine hemorrhagic fever,"['Argentinian hemorrhagic fever', 'Junin hemorrhagic fever']",0050194,,319223,C0019097,,,,,,,,
mondo:0017875,Bolivian hemorrhagic fever,['Machupo hemorrhagic fever'],0050195,,319229,C0282192,,,,,,,10005932,
mondo:0017876,Venezuelan hemorrhagic fever,['Guanarito hemorrhagic fever'],0050196,,319234,C0042470,,,,,,,,
mondo:0017877,Brazilian hemorrhagic fever,['Sabia hemorrhagic fever'],0050197,,319239,C0343633,,,,,,,,
mondo:0017878,Chapare hemorrhagic fever,,0050198,,319244,CN203927,,,,,,,,
mondo:0017879,hantavirus pulmonary syndrome,"['Hantavirus', 'Hantavirus-associated respiratory distress syndrome', 'HARDS', 'four corners hantavirus']",14472,,319247,C0243025,,C84747,0007296,D018804,480.8,,10019143,
mondo:0017880,Rift valley fever,['RVF'],1328,,319251,C0035613,,C128419,,D012295,,A92.4,10039143,
mondo:0017881,Kyasanur forest disease,"['KFD virus', 'monkey disease', 'Kyasanur hemorrhagic fever', 'monkey fever', 'Kyasanur forest disease virus caused disease or disorder', 'KFD']",11320,,319254,C0022810,,,,D007733,065.2,A98.2,10023505,
mondo:0017882,Omsk hemorrhagic fever,,992,,319266,C0019103,,,,D006481,065.1,A98.1,10030310,
mondo:0017884,papillary renal cell carcinoma,"['chromophil carcinoma of kidney', 'renal adenocarcinoma', 'papillary renal cell carcinoma, familial - (subtype)', 'papillary renal cell carcinoma, bilateral - (subtype)', 'RCCP1', 'HPRCC', 'chromophil carcinoma of the kidney', 'papillary (chromophil) renal cell carcinoma', 'papillary kidney carcinoma', 'papillary renal cell cancer', 'papillary renal cell adenocarcinoma', 'sporadic papillary renal cell carcinoma', 'renal cell carcinoma, papillary, type 1', 'RCCP', 'renal cell carcinoma, papillary, 1', 'papillary renal cell carcinoma', 'papillary renal carcinoma, malignant - (subtype)', 'papillary renal cell carcinoma, multiple - (subtype)', 'chromophil renal cell carcinoma', 'chromophil RCC', 'papillary renal cell carcinoma, sporadic - (subtype)']",4465,,319298,CN205129,"['0.0976', '-0.1973', '0.1562', '0.2334', '0.006054', '-0.2122', '0.222', '0.6934', '-0.1754', '0.0333', '-0.1173', '0.28', '-0.2151', '0.1339', '-0.4658', '-0.05838', '0.02354', '-0.715', '0.809', '-0.4988', '0.00074', '-0.5283', '0.474', '-0.2134', '0.4917', '0.07904', '0.355', '-0.01883', '-0.1418', '0.06647', '0.6045', '-0.04358', '0.5195', '-0.2913', '-0.3037', '-0.2', '-0.34', '-0.0667', '0.10876', '0.445', '-0.1792', '-0.001482', '0.3665', '-0.534', '0.3892', '-0.455', '-0.7437', '-0.435', '0.0631', '-0.0821', '0.2', '0.4197', '-0.232', '-0.4468', '-0.3518', '-0.1464', '0.1742', '-0.2013', '-0.849', '-0.1376', '0.2374', '0.08044', '-0.323', '-0.2307', '0.1538', '0.3757', '0.7407', '0.0859', '0.02597', '0.825', '-0.2104', '0.02141', '-0.3352', '-0.2185', '0.674', '-0.138', '-0.1948', '-0.06042', '0.1915', '-0.4736', '-0.2764', '0.1142', '-0.0838', '-0.1326', '-0.723', '-0.527', '0.577', '0.1312', '-0.11676', '-0.0795', '0.1862', '-0.01297', '-0.05917', '-0.3435', '0.6113', '0.05466', '0.399', '-0.6094', '-0.2231', '-0.07947']",C6975,0000640,,,,,
mondo:0017885,chromophobe renal cell carcinoma,"['chromophobe renal cell carcinoma', 'chromophobe carcinoma of the kidney', 'CHRCC', 'chromophobe cell carcinoma of the kidney', 'kidney chromophobe', 'renal cell carcinoma, chromophobe type', 'chromophobe carcinoma', 'chromophobe cell carcinoma of kidney', 'CRCC', 'ChRCC', 'chromophobe renal cell adenocarcinoma', 'chromophobe renal cell cancer', 'renal cell carcinoma, chromophobe cell', 'chromophobe carcinoma of kidney', 'chromophobe adenocarcinoma']",4471,,319303,C3887514,,C4146,0000335,,,,,
mondo:0017886,MIT family translocation renal cell carcinoma,"['translocation renal cell carcinoma', 'carcinoma associated with MITF/TFE translocation']",,,319308,C4518356,,,,,,,,
mondo:0017887,renal cell carcinoma associated with neuroblastoma,"['renal cell cancer associated with neuroblastoma', 'renal cell carcinoma after neuroblastoma', 'renal cell carcinoma associated with neuroblastoma']",,,319314,C3272295,,C100051,,,,,,
mondo:0017890,tubulocystic renal cell carcinoma,['Tubulocystic renal cell cancer'],,,319325,C4288091,,C126303,,,,,,
mondo:0017891,inherited renal cancer-predisposing syndrome,,,,319328,CN203941,,,,,,,,
mondo:0017892,autosomal recessive myogenic arthrogryposis multiplex congenita,"['autosomal recessive myogenic AMC', 'SYNE1-related arthrogryposis multiplex congenita', 'SYNE1-related AMC']",,,319332,CN203942,"['-0.723', '0.1484', '0.0585', '-0.0701', '0.0918', '-0.6597', '0.1433', '1.092', '-0.949', '-0.2258', '-0.2947', '-0.06757', '0.1095', '0.3706', '0.2988', '0.294', '0.345', '-0.4368', '-0.2583', '-1.023', '-0.1392', '-0.1385', '0.1428', '0.1311', '-0.06696', '0.218', '0.09564', '0.6543', '-0.2808', '0.1973', '0.1857', '0.3442', '0.1329', '0.53', '-0.10803', '-0.1992', '-0.03995', '-0.1088', '-0.1137', '0.07684', '-0.9497', '-0.1571', '-0.2756', '0.7593', '-0.3147', '-0.1724', '-0.4902', '0.283', '0.05997', '0.1904', '0.04294', '0.2678', '-0.319', '-0.3047', '0.1948', '-0.582', '-0.0758', '-0.515', '-0.187', '0.2141', '-0.2147', '-0.4102', '0.3838', '0.535', '-0.837', '-0.12225', '0.6177', '0.4746', '-0.195', '0.36', '-0.225', '0.2192', '0.508', '-0.1172', '0.5396', '-0.3364', '0.5054', '0.7266', '-0.4788', '-0.4626', '-0.4219', '-0.11584', '0.862', '0.6562', '-0.1292', '0.1057', '0.01862', '0.2152', '0.1365', '-0.03195', '0.2007', '0.6025', '0.3394', '0.501', '0.3376', '0.618', '0.5444', '-0.3164', '0.5366', '0.388']",,,,,,,
mondo:0017893,inherited acute myeloid leukemia,"['familial AML', 'Pure familial acute myeloid leukaemia', 'hereditary acute myeloid leukemia', 'Pure familial acute myeloid leukemia', 'inherited AML', 'Pure familial AML', 'hereditary acute myeloid leukaemia']",,,319465,CN203946,,,,,,,,
mondo:0017894,acute myeloid leukemia with CEBPA somatic mutations,"['AML with CEBPA somatic mutations', 'acute myeloid Leukaemia with mutated CEBPA', 'non-familial acute myeloid leukaemia with mutated CEBPA', 'acute myeloid Leukemia with non-germline mutated CEBPA', 'non-familial acute myeloid leukemia with mutated CEBPA', 'acute myeloid Leukemia with mutated CEBPA', 'acute myeloid Leukaemia with non-germline mutated CEBPA', 'AML with mutated CEBPA']",0081095,,319480,C2826178,,C82433,,,,,,
mondo:0017895,familial papillary or follicular thyroid carcinoma,"['familial nonmedullary thyroid gland carcinoma', 'FNMTC', 'familial pure nonmedullary thyroid carcinoma']",,,319487,CN227215,,C118829,,,,,,
mondo:0017896,familial nonmedullary thyroid carcinoma,"['thyroid cancer, nonmedullary']",,,319494,CN227216,,,,,,,,
mondo:0017900,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to complete IFNgammaR2 deficiency,"['MSMD due to complete IFNgammaR2 deficiency', 'Mendelian susceptibility to mycobacterial diseases due to complete interferon gamma receptor 2 deficiency', 'MSMD due to complete interferon gamma receptor 2 deficiency', 'IFNGR2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency']",,,319547,CN203956,"['0.1337', '0.1844', '0.1821', '-0.4204', '0.3633', '-0.613', '0.672', '-0.1534', '0.1736', '-0.5864', '0.1329', '0.3196', '-0.682', '0.1671', '0.2542', '-0.1389', '-0.1216', '-0.005836', '-0.301', '-0.36', '-0.3005', '-0.687', '0.7466', '-0.4106', '-0.625', '0.4263', '-0.3184', '0.1438', '-0.3674', '0.0401', '0.1135', '0.1511', '0.604', '0.3306', '-0.188', '-0.602', '-0.773', '-0.0873', '-0.3455', '-0.0298', '0.2119', '-0.3286', '0.6', '-0.385', '-0.2354', '-0.3599', '-0.3567', '-0.12256', '0.4104', '0.2347', '0.5435', '-0.689', '0.7007', '0.2324', '-0.2124', '0.1293', '0.3171', '-0.559', '0.004177', '0.358', '0.2008', '0.2029', '-0.00797', '-0.2421', '0.4624', '-0.11774', '0.579', '0.0926', '0.334', '0.7974', '0.1283', '-0.533', '-0.4434', '-0.4722', '0.2847', '0.3113', '0.08887', '-0.1763', '-0.295', '-0.278', '-0.7417', '0.544', '-0.154', '0.327', '-0.2219', '0.1517', '0.5103', '0.482', '0.9556', '-0.2201', '0.758', '0.7046', '-0.6313', '-0.6304', '0.743', '0.534', '0.1903', '-0.4268', '0.3389', '0.07043']",,,,,,,
mondo:0017901,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency,"['autosomal recessive MSMD due to partial IFNgammaR1 deficiency', 'autosomal recessive MSMD due to partial interferon gamma receptor 1 deficiency', 'autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency', 'IFNGR1 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency']",,,319569,CN203960,"['0.05948', '0.3528', '0.0459', '-0.3164', '0.3223', '-0.6733', '0.4946', '-0.159', '0.6484', '-0.5513', '0.3184', '0.08905', '-0.2764', '0.2622', '0.4846', '-0.04596', '0.03036', '-0.12054', '-0.2322', '-0.6333', '-0.1777', '-0.2384', '0.5674', '-0.1071', '-0.7554', '0.4893', '-0.824', '-0.0916', '-0.1637', '-0.796', '0.06085', '-0.01559', '0.4666', '0.309', '0.04138', '-0.807', '-0.42', '-0.2499', '-0.6123', '-0.4336', '-0.01457', '-0.3477', '0.361', '-0.11615', '-0.1976', '-0.204', '-0.05234', '-0.4167', '-0.05685', '0.4946', '0.2007', '-0.4944', '0.1299', '-0.0909', '-0.223', '0.3223', '0.6704', '-0.4377', '-0.2424', '0.7583', '0.00705', '0.693', '0.2864', '0.283', '0.679', '0.478', '0.1655', '0.03833', '-0.251', '0.4211', '0.06464', '-0.28', '-0.006466', '-0.4807', '0.546', '0.912', '0.4006', '-0.2993', '-0.2069', '0.3376', '-0.529', '0.56', '0.3818', '0.7485', '-0.05478', '0.1116', '0.616', '0.437', '0.6206', '-0.05338', '0.689', '0.3503', '-0.5386', '-0.2786', '0.7734', '0.9385', '0.4438', '-0.4602', '0.1567', '-0.2874']",,,,,,,
mondo:0017902,autosomal recessive Mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency,"['IFNGR2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency', 'autosomal recessive MSMD due to partial interferon gamma receptor 2 deficiency', 'autosomal recessive MSMD due to partial IFNgammaR2 deficiency', 'autosomal recessive mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency']",,,319574,CN203961,"['-0.0827', '0.2196', '0.1783', '-0.3018', '0.1425', '-0.6113', '0.4546', '-0.348', '0.4219', '-0.573', '0.2542', '-0.1233', '-0.3003', '-0.03488', '0.3816', '-0.10364', '0.2275', '-0.2474', '-0.397', '-0.8135', '-0.337', '0.02791', '0.7056', '-0.321', '-0.6514', '0.466', '-0.7256', '-0.03543', '-0.3357', '-0.6504', '-0.06696', '0.0718', '0.5854', '0.0625', '-0.1371', '-0.6357', '-0.4324', '-0.262', '-0.4924', '-0.4788', '0.1226', '-0.1841', '0.3752', '-0.1636', '-0.4094', '-0.471', '0.0618', '-0.2651', '0.0863', '0.5474', '0.239', '-0.456', '0.3923', '-0.0635', '-0.2273', '-0.14', '0.489', '-0.3325', '-0.2478', '0.4543', '0.1685', '0.502', '0.3767', '0.2303', '0.6074', '0.2072', '0.2413', '0.10974', '-0.3494', '0.536', '-0.08246', '-0.0742', '0.1915', '-0.10114', '0.318', '0.702', '0.4573', '0.0252', '-0.2932', '0.3296', '-0.4563', '0.2913', '0.0351', '0.69', '0.1031', '0.3384', '0.3633', '0.3264', '0.6475', '-0.1018', '0.725', '0.465', '-0.3665', '-0.2957', '0.9', '0.947', '0.3303', '-0.4697', '0.04346', '0.0373']",,,,,,,
mondo:0017903,autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR2 deficiency,"['IFNGR2 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency', 'autosomal dominant MSMD due to partial interferon gamma receptor 2 deficiency', 'autosomal dominant MSMD due to partial IFNgammaR2 deficiency', 'autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 2 deficiency']",,,319589,CN203963,,,,,,,,
mondo:0017904,steroid dehydrogenase deficiency-dental anomalies syndrome,"['severe dental aberrations in familial steroid dehydrogenase deficiency', 'Lyngstadaas syndrome', 'steroid dehydrogenase deficiency dental anomalies']",,,3196,C2931508,,,,C537490,,,,
mondo:0017905,X-linked Mendelian susceptibility to mycobacterial diseases,"['X-linked MSMD', 'mendelian susceptibility to mycobacterial diseases, X-linked']",,,319605,CN203967,"['-0.1683', '0.2734', '-0.2256', '-0.7754', '0.3608', '-0.03555', '0.5674', '0.1317', '0.614', '-0.7817', '-0.0958', '0.2406', '-0.473', '0.457', '0.6694', '0.794', '-0.5977', '-0.4155', '-0.3857', '-0.5786', '0.02199', '-0.455', '0.7817', '0.1471', '-0.4321', '-0.337', '-1.266', '-0.3267', '-0.0903', '-0.4302', '0.1937', '0.8193', '0.623', '0.07635', '0.4727', '-0.2434', '0.3428', '-0.4768', '-0.288', '-0.5425', '0.665', '-0.3535', '0.00924', '-0.3289', '-0.28', '-0.2637', '-0.3198', '-0.6416', '1.126', '0.3914', '-0.06934', '-0.5435', '0.4907', '0.3804', '-0.1414', '0.10156', '1.117', '-0.5757', '0.7593', '0.531', '0.0318', '0.2068', '-0.01021', '0.3596', '-0.05228', '0.0702', '0.695', '0.4565', '0.307', '0.4304', '-0.1187', '-0.566', '-0.03342', '0.3162', '0.5503', '0.1372', '0.2598', '0.0733', '-0.05496', '0.3992', '-0.3276', '0.2262', '-0.10486', '0.09955', '-0.511', '-0.251', '0.5547', '0.7314', '0.9546', '-0.4019', '0.4832', '0.6875', '-0.7725', '-0.2169', '0.9077', '0.68', '-0.3862', '-0.7896', '-0.2605', '-0.039']",,,,,,,
mondo:0017906,amyloidosis cutis dyschromia,['amyloidosis cutis dyschromica'],0080932,,319635,,"['0.4878', '-0.6646', '-0.3645', '-0.1245', '0.2903', '-0.4053', '-0.5894', '0.286', '-1.309', '0.09344', '-0.2737', '0.011475', '-0.8994', '0.01063', '-0.77', '0.0635', '0.2397', '-0.3909', '0.11017', '-0.792', '0.4111', '0.0701', '0.5796', '0.0088', '0.1471', '0.437', '-0.641', '-0.5566', '0.1593', '0.114', '0.847', '-0.4924', '1.04', '-0.7026', '0.4875', '-0.707', '-0.3428', '-0.11896', '0.3015', '0.3843', '0.1825', '-0.3252', '-0.3374', '0.5493', '0.499', '-0.2043', '-0.789', '0.3318', '0.1707', '0.636', '-0.2192', '0.6743', '0.332', '-0.2886', '-0.816', '-0.1067', '0.49', '-0.00864', '-0.6436', '-0.7764', '-0.2163', '0.4016', '0.6396', '-0.7144', '-0.08813', '-0.1487', '0.6816', '1.218', '-0.4077', '0.612', '-0.4397', '0.4666', '-0.2114', '-0.1403', '0.08875', '0.5566', '-0.3271', '0.9824', '-0.3147', '-1.094', '-0.2786', '-0.1975', '0.139', '-0.1153', '0.2487', '-0.7705', '-0.2', '-0.2323', '0.4797', '-0.1406', '0.82', '-0.1637', '-0.326', '-0.2932', '0.577', '0.3352', '-0.751', '-0.1714', '0.1592', '0.26']",,,,,,,
mondo:0017907,primary lymphoma of the conjunctiva,"['primary lymphoid conjunctival tumour', 'primary lymphoid conjunctival tumor', 'primary organ-specific lymphoma of conjunctiva', 'conjunctiva lymphoma', 'conjunctiva primary organ-specific lymphoma']",,,319667,CN203974,,,,,,,,
mondo:0017909,inherited glutathione synthetase deficiency,"['pyroglutamicaciduria', 'inborn error of glutathione synthase activity', 'rare inborn error of glutathione synthase activity', 'oxoprolinase deficiency', '5-oxoprolinuria', 'pyroglutamic aciduria', 'glutathione synthetase deficiency', 'GSSD']",0080699,,32,C0398746,"['-0.6562', '0.1006', '-0.4583', '0.3115', '0.1901', '-0.3306', '-0.1222', '0.3196', '-0.12286', '0.008766', '-0.1593', '-0.3022', '0.1147', '0.009895', '-0.1381', '-0.2534', '-0.0392', '0.2017', '-0.4895', '-0.5693', '0.115', '-0.1816', '0.6885', '-0.02077', '0.00606', '-0.5566', '-0.2515', '-0.01316', '-0.532', '-0.3306', '-0.0777', '0.612', '0.2456', '0.5903', '0.0149', '-0.4297', '-0.3901', '-0.4753', '-0.2842', '0.1198', '-0.1582', '-0.4026', '0.3147', '-0.11993', '-0.359', '-0.251', '-0.1656', '-0.1588', '-0.0452', '0.03955', '-0.3967', '-0.34', '0.544', '-0.1131', '-0.0134', '-0.03323', '0.722', '-0.509', '-0.3315', '0.4336', '-0.1252', '0.528', '0.4802', '-0.11615', '0.01697', '-0.1554', '0.069', '0.2421', '-0.28', '0.0898', '0.2207', '-0.1564', '-0.3577', '-0.2452', '0.4895', '0.1073', '0.5356', '-0.0758', '0.0798', '0.3145', '-0.11224', '-0.5767', '-0.0141', '0.4182', '0.722', '0.3857', '-0.2434', '0.0002407', '0.3599', '0.007538', '0.6255', '0.2046', '-0.0946', '-0.764', '0.602', '1.27', '0.2834', '-0.7046', '-0.4685', '-0.1926']",C128193,,C536835,,,,
mondo:0017910,dehydrated hereditary stomatocytosis,"['Desiccytosis hereditary', 'xerocytosis hereditary', 'hereditary xerocytosis']",0111575,,3202,,"['-0.551', '-0.04364', '-0.0555', '-0.2803', '0.1425', '-0.3184', '-0.3416', '1.062', '0.667', '-0.3074', '-0.572', '0.2135', '0.1765', '-0.125', '-0.51', '-0.2316', '-0.3977', '-0.4111', '0.501', '-0.994', '-0.09973', '-0.3003', '0.542', '0.057', '-0.2167', '0.658', '0.1775', '0.2279', '0.07263', '-0.04355', '-0.02194', '-0.323', '0.7036', '0.2668', '-1.099', '0.0989', '-0.3381', '-0.1764', '0.6846', '-0.01616', '-0.02663', '-0.1348', '0.754', '-0.5264', '-0.0585', '-0.3103', '-0.516', '-0.2532', '0.1432', '-0.2761', '0.1554', '0.1166', '0.5723', '-0.02847', '0.01863', '0.3413', '0.5493', '-0.02483', '-0.1444', '0.2712', '0.238', '-0.2095', '0.369', '-0.7183', '-0.1766', '0.0931', '0.533', '0.3997', '-0.3745', '0.838', '0.1876', '0.3718', '-0.758', '-0.1304', '0.5337', '0.011246', '0.07404', '-0.1809', '-0.05933', '0.1628', '-0.2156', '0.2051', '0.2356', '-0.0262', '0.33', '0.11334', '0.3467', '0.3215', '0.1969', '-0.6597', '0.5938', '-0.1476', '-0.06012', '-0.0793', '0.684', '0.796', '0.519', '-0.3953', '-0.0256', '-0.1635']",,,,,,,
mondo:0017912,X-linked pure spastic paraplegia,,,,320332,,,,,,,,,
mondo:0017913,pure or complex hereditary spastic paraplegia,"['Pure or complicated hereditary spastic paraplegia', 'Pure or complicated familial spastic paraplegia', 'Pure or complex familial spastic paraplegia']",,,320335,CN227219,,,,,,,,
mondo:0017914,pure or complex autosomal dominant spastic paraplegia,['Pure or complicated autosomal dominant spastic paraplegia'],,,320342,,,,,,,,,
mondo:0017915,pure or complex autosomal recessive spastic paraplegia,['Pure or complicated autosomal recessive spastic paraplegia'],,,320346,,,,,,,,,
mondo:0017916,pure or complex X-linked spastic paraplegia,['Pure or complicated X-linked spastic paraplegia'],,,320350,,,,,,,,,
mondo:0017917,maternally-inherited spastic paraplegia,"['maternally-inherited SPG', 'MT-ATP6-related mitochondrial spastic paraplegia']",,,320360,,,,,,,,,
mondo:0017918,white matter hypoplasia-corpus callosum agenesis-intellectual disability syndrome,"['Curatolo-Cilio-Pessagno syndrome', 'Curatolo Cilio Pessagno syndrome', 'familial white matter hypoplasia, agenesis of the corpus callosum, intellectual disability and growth deficiency']",,,3207,C2931292,,,,C536701,,,,
mondo:0017919,exstrophy-epispadias complex,"['OEIS complex', 'OEIS syndrome', 'bladder exstrophy-epispadias-cloacal extrophy complex', 'BEEC', 'EEC']",0080173,258040,322,C1850321,,C99142,,,,,,
mondo:0017920,deafness-genital anomalies-metacarpal and metatarsal synostosis syndrome,"['sensorineural deafness, hypospadias, and synostosis of metacarpals and metatarsals 4 and 5', 'short stature, intellectual disability and multiple dysmorphisms', 'Pfeiffer-Kapferer syndrome', 'Pfeiffer Kapferer syndrome', 'short stature, mental retardation and multiple dysmorphisms']",,,3224,C2931654,,,,C537887,,,,
mondo:0017921,hearing loss-familial salivary gland insensitivity to aldosterone syndrome,"['hearing loss and familial salivary gland insensitivity to aldosterone', 'Tunglang savage Bellman syndrome', 'hearing loss insensitivity to aldosterone', 'Tungland-Bellman syndrome']",,,3225,,,,,C536927,,,,
mondo:0017922,deafness-onychodystrophy syndrome,,,,3231,CN204041,"['-0.0129', '0.0972', '0.419', '-0.3003', '0.1027', '-0.4014', '0.0447', '0.3152', '-0.176', '-0.4587', '-0.3054', '-0.2964', '0.0936', '0.11676', '-0.1', '0.1643', '0.175', '-0.11127', '0.0582', '-0.4944', '0.2443', '0.1621', '0.2234', '-0.0649', '0.2046', '0.1317', '-0.32', '-0.06885', '0.3071', '-0.2976', '0.07214', '0.05978', '0.3477', '0.454', '0.1049', '-0.2122', '-0.00526', '-0.339', '-0.3086', '-0.382', '0.08905', '-0.2343', '0.02922', '0.04254', '0.186', '-0.3718', '0.18', '0.4172', '0.0338', '0.1261', '-0.1942', '0.1534', '-0.02187', '-0.1234', '-0.2479', '-0.3743', '-0.1304', '0.02884', '-0.10065', '0.1592', '0.1351', '-0.0007954', '-0.1073', '0.1317', '-0.1313', '0.013794', '-0.03976', '0.2219', '-0.2808', '0.2664', '-0.4023', '0.1177', '0.1927', '0.0376', '0.1753', '0.0565', '0.3083', '-0.1653', '-0.4316', '-0.03604', '0.10077', '0.1622', '-0.1014', '0.5107', '0.01434', '-0.2006', '0.005444', '0.4434', '0.1416', '-0.00999', '0.3467', '0.4697', '0.173', '0.1192', '0.2472', '0.0717', '0.3516', '-0.3677', '0.3467', '0.3809']",,,,,,,
mondo:0017923,multiple synostoses syndrome,"['WL syndrome', 'facio-audio-symphalangism', 'symphalangism-brachydactyly syndrome', 'deafness-Hermann type symphalangism syndrome']",0050794,,3237,CN204052,"['-0.2754', '-0.10925', '0.2915', '-0.1757', '0.1929', '-0.4126', '-0.02121', '0.3914', '-0.4602', '-0.1426', '-0.1099', '0.0648', '-0.0914', '-0.01106', '-0.0649', '-0.1197', '0.1713', '-0.1056', '0.05933', '-0.4456', '-0.05032', '0.03537', '0.3296', '-0.1626', '0.1653', '0.2191', '0.064', '0.03616', '0.0617', '-0.08777', '-0.02246', '-0.2115', '0.1818', '0.1433', '0.2576', '-0.264', '0.1154', '-0.2815', '-0.01608', '-0.3203', '-0.01212', '-0.333', '0.03476', '-0.0384', '0.2245', '-0.3013', '-0.1963', '0.488', '0.06082', '0.0758', '-0.1123', '-0.01428', '0.2686', '0.076', '-0.4023', '-0.305', '-0.004646', '0.02702', '-0.1395', '-0.0747', '0.4053', '0.04224', '-0.241', '-0.04694', '-0.153', '-0.0862', '0.1732', '0.3755', '-0.1412', '0.10284', '-0.3682', '0.00925', '0.05643', '-0.2217', '0.01003', '0.08685', '-0.1045', '0.1404', '-0.3394', '-0.2637', '-0.2086', '0.2245', '0.1124', '0.3518', '-0.00994', '-0.0506', '-0.2725', '0.2228', '0.1522', '-0.2166', '-0.06076', '0.1187', '0.1545', '0.0005665', '0.2004', '-0.004337', '0.5986', '-0.4634', '0.3855', '0.1407']",,,,,,,
mondo:0017924,central nervous system calcification-deafness-tubular acidosis-anemia syndrome,['Yoshimura-Takeshita syndrome'],,,3240,CN204056,,,,,,,,
mondo:0017925,T-cell immunodeficiency with epidermodysplasia verruciformis,['T-cell immunodeficiency due to RHOH deficiency'],,,324294,CN714013,,,,,,,,
mondo:0017926,multiple paragangliomas associated with polycythemia,"['paraganglioma-somatostatinoma-polycythemia syndrome', 'multiple paragangliomas associated with erythrocytosis']",,,324299,CN204064,,,,,,,,
mondo:0017927,severe lateral tibial bowing with short stature,,,,324307,CN204066,,,,,,,,
mondo:0017928,9p13 microdeletion syndrome,"['monosomy 9p13', 'Del(9)(p13)']",,,324313,CN204067,,,,,,,,
mondo:0017929,congenital achiasma,,,,324353,,,,,,,H47.4,,
mondo:0017930,mixed sclerosing bone dystrophy with extra-skeletal manifestations,,,,324364,,,,,,,,,
mondo:0017931,hereditary inclusion body myopathy type 4,['HIBM4'],,,324381,CN227223,,,,,,,,
mondo:0017932,muscular hypertrophy-hepatomegaly-polyhydramnios syndrome,,,,324416,CN204070,,,,,,,,
mondo:0017933,hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation,['hypertrophic cardiomyopathy and renal tubular disease due to mtDNA mutation'],,,324525,CN204073,,,,,,,,
mondo:0017934,aphonia-deafness-retinal dystrophy-bifid halluces-intellectual disability syndrome,"['aphonia-deafness-retinal dystrophy-duplicated halluces-intellectual disability syndrome', 'aphonia-hearing loss-retinal dystrophy-duplicated halluces-intellectual disability syndrome']",,,324540,CN204076,,,,,,,,
mondo:0017935,hyperinsulinism due to HNF1A deficiency,['hyperinsulinemic hypoglycemia due to HNF1A deficiency'],,,324575,C4303475,,,,,,,,
mondo:0017936,benign Samaritan congenital myopathy,,,,324581,,,,,,,,,
mondo:0017937,autosomal dominant intermediate Charcot-Marie-Tooth disease with neuropathic pain,,,,324585,CN204081,,,,,,,,
mondo:0017939,minicore myopathy,"['classic multiminicore disease', 'classic multiminicore myopathy', 'classic MmD']",,,324604,CN204085,"['-0.1148', '0.0885', '-0.006', '-0.0562', '0.0465', '-0.1427', '-0.03278', '0.1108', '-0.0681', '-0.01447', '-0.062', '-0.0345', '0.01729', '0.0419', '-0.012405', '-0.04642', '-0.04446', '-0.03848', '-0.03854', '-0.2135', '-0.006012', '-0.06775', '0.0917', '0.02357', '0.03558', '-0.01024', '-0.01143', '-0.05222', '-0.01631', '-0.04993', '0.09393', '0.010185', '0.0729', '0.07996', '0.01167', '-0.031', '-0.04736', '-0.05475', '-0.02454', '-0.11316', '0.001712', '-0.1421', '0.00947', '0.00736', '0.0339', '-0.08405', '-0.02995', '0.08203', '-0.01133', '0.0668', '-0.04803', '-0.006504', '0.05374', '-0.02913', '-0.05048', '-0.08887', '0.1118', '-0.06445', '-0.05453', '0.01985', '0.0829', '0.02672', '0.00918', '0.03198', '0.01501', '0.01707', '0.0922', '0.0772', '-0.11554', '0.11176', '-0.12115', '-0.008224', '0.05084', '-0.03412', '0.04266', '0.02379', '-0.01317', '-0.0321', '-0.0529', '-0.05466', '0.0473', '-0.00745', '-0.05005', '0.08777', '0.0153', '0.0666', '0.02116', '0.05658', '0.07996', '-0.01672', '0.0795', '0.065', '0.04562', '0.03348', '0.1802', '0.0395', '0.0866', '-0.10706', '-0.01369', '-7.01e-05']",,,,,,,
mondo:0017940,autosomal dominant Charcot-Marie-Tooth disease type 2 due to KIF5A mutation,['CMT2 due to KIF5A mutation'],,,324611,CN204086,,,,,,,,
mondo:0017941,chikungunya,"['Chikungunya virus infection', 'CHIK', 'arbovirus A Chikungunya type', 'Chikungunya fever', 'Chikungunya virus caused disease or disorder', 'CHIKV infection', 'CK']",0050012,,324625,C0008055,,C128422,,D065632,,,,
mondo:0017942,Hendra virus infection,['Hendra henipavirus caused disease or disorder'],,,324632,,,,,,,,,
mondo:0017943,autoerythrocyte sensitization syndrome,"['psychogenic purpura', 'GDS', 'Autoerythrocyte sensitization purpura', 'Autoerythrocyte sensitization', 'Gardner-Diamond syndrome', 'painful bruising syndrome']",,,324636,C0301928,,,,C535645,287.2,,,
mondo:0017944,invasive non-typhoidal salmonellosis,"['iNTS disease', 'invasive non-typhoidal salmonella disease']",,,324648,,,,,,,,,
mondo:0017945,ABetaL34V amyloidosis,"['ABetaL34V-related amyloidosis', 'HCHWA, Piedmont type', 'hereditary cerebral hemorrhage with amyloidosis, Piedmont type', 'hereditary cerebral haemorrhage with amyloidosis, Piedmont type', 'ABeta amyloidosis, Piedmont type']",,,324703,,"['0.5264', '-0.6323', '-0.696', '0.10657', '-0.0004656', '-0.286', '-0.655', '0.63', '-1.543', '-0.02704', '-0.3623', '0.06006', '-1.016', '-0.04227', '-0.4248', '-0.4087', '0.0408', '-0.2173', '0.05914', '-0.7075', '0.4414', '0.04056', '0.4282', '-0.0289', '0.2234', '0.5957', '-0.7627', '0.03293', '0.6216', '0.3562', '0.2499', '-0.4875', '1.0205', '-0.9673', '0.665', '-0.585', '-0.471', '0.3462', '0.2502', '-0.007557', '0.2247', '-0.3484', '-0.2124', '0.2444', '0.501', '-0.59', '-0.5605', '0.4644', '0.2783', '0.868', '0.2344', '0.73', '0.2522', '-0.2654', '-0.5015', '0.01317', '0.732', '-0.03256', '-0.2832', '-0.727', '-0.632', '0.426', '0.6084', '-0.93', '0.3896', '-0.428', '0.4238', '0.851', '-0.609', '0.382', '-0.185', '0.4612', '-0.5264', '-0.0886', '0.3545', '0.8105', '-0.361', '1.415', '-0.36', '-0.757', '-0.453', '-0.4924', '-0.004673', '-0.142', '0.2175', '-0.728', '-0.12415', '0.08044', '0.1815', '-0.2274', '0.6147', '-0.2673', '-0.514', '-0.4702', '0.507', '0.7944', '-0.3718', '-0.3096', '0.0946', '0.11194']",,,,,,,
mondo:0017946,"ABeta amyloidosis, Iowa type","['hereditary cerebral hemorrhage with amyloidosis, Iowa type', 'HCHWA, Iowa type', 'hereditary cerebral haemorrhage with amyloidosis, Iowa type', 'ABetaD23N amyloidosis', 'cerebral amyloid angiopathy, APP-related, Iowa variant']",,,324708,,"['0.3345', '-0.455', '-0.5854', '0.11194', '0.0166', '-0.454', '-0.6904', '0.553', '-1.543', '-0.04218', '-0.3154', '-0.0531', '-1.142', '0.1414', '-0.2854', '-0.2773', '0.1249', '-0.3098', '0.0859', '-0.594', '0.4897', '0.2034', '0.05878', '0.1205', '0.4062', '0.5923', '-0.504', '-0.04333', '0.5483', '0.217', '0.2903', '-0.4812', '1.23', '-1.0205', '0.7925', '-0.642', '-0.609', '0.322', '0.2183', '-0.1714', '0.5044', '-0.4678', '-0.1608', '0.372', '0.466', '-0.296', '-0.4602', '0.54', '0.388', '0.8486', '0.2123', '1.036', '0.2031', '-0.3423', '-0.3792', '0.0614', '0.4849', '-0.081', '-0.384', '-0.642', '-0.621', '0.4517', '0.8237', '-0.948', '0.379', '-0.442', '0.4011', '0.821', '-0.5913', '0.2258', '0.004684', '0.5303', '-0.4822', '0.04224', '0.3784', '0.7505', '-0.2578', '1.144', '-0.4187', '-0.9062', '-0.4333', '-0.6543', '0.1774', '-0.3013', '0.2299', '-0.7256', '-0.232', '0.1313', '0.3123', '-0.0956', '0.532', '-0.2869', '-0.452', '-0.546', '0.4329', '0.651', '-0.3462', '-0.0695', '0.1262', '0.3613']",,,,,,,
mondo:0017947,"ABeta amyloidosis, Italian type","['HCHWA, Italian type', 'cerebral amyloid angiopathy, APP-related, Italian variant', 'ABetaE22K amyloidosis', 'hereditary cerebral haemorrhage with amyloidosis, Italian type', 'hereditary cerebral hemorrhage with amyloidosis, Italian type']",,,324713,,"['0.357', '-0.685', '-0.628', '0.2241', '-0.002512', '-0.369', '-0.645', '0.4583', '-1.505', '-0.07007', '-0.2113', '-0.01724', '-1.072', '0.1231', '-0.33', '-0.3533', '0.012596', '-0.3289', '0.0708', '-0.582', '0.376', '-0.03268', '0.29', '-0.02509', '0.02322', '0.4775', '-0.4963', '-0.1896', '0.672', '0.4607', '0.3735', '-0.499', '0.9355', '-0.886', '0.716', '-0.5684', '-0.655', '0.2068', '0.1213', '-0.03992', '0.3943', '-0.316', '-0.3083', '0.3289', '0.4543', '-0.5117', '-0.456', '0.573', '0.504', '0.7275', '0.349', '0.6206', '0.2156', '-0.355', '-0.5596', '-0.0637', '0.6216', '0.07635', '-0.4165', '-0.799', '-0.5684', '0.5615', '0.6724', '-1.027', '0.3887', '-0.3132', '0.3467', '0.811', '-0.712', '0.4695', '-0.258', '0.4067', '-0.4678', '-0.1597', '0.3591', '0.8833', '-0.549', '1.299', '-0.4424', '-0.7026', '-0.5757', '-0.403', '-0.02316', '-0.1604', '0.2588', '-0.5273', '-0.0873', '0.0508', '0.2952', '-0.2917', '0.5786', '-0.4014', '-0.447', '-0.3713', '0.7725', '0.4749', '-0.3794', '-0.2037', '0.06204', '0.1521']",,,,,,,
mondo:0017948,ABetaA21G amyloidosis,"['ABetaA21G-related amyloidosis', 'HCHWA, Flemish type', 'ABeta amyloidosis, Flemish type', 'cerebral amyloid angiopathy, APP-related, Flemish variant', 'hereditary cerebral haemorrhage with amyloidosis, Flemish type', 'hereditary cerebral hemorrhage with amyloidosis, Flemish type']",,,324718,,"['0.2883', '-0.6914', '-0.5854', '0.1295', '0.03238', '-0.54', '-0.7373', '0.508', '-1.432', '-0.08966', '-0.1975', '0.08405', '-1.04', '0.11975', '-0.391', '-0.521', '0.07245', '-0.2319', '0.03026', '-0.5938', '0.531', '-0.0963', '0.2976', '0.1685', '0.1037', '0.6475', '-0.4436', '-0.02557', '0.608', '0.2874', '0.449', '-0.4822', '0.911', '-0.7065', '0.6655', '-0.697', '-0.6045', '0.2393', '0.1913', '-0.0355', '0.325', '-0.4985', '-0.1884', '0.2783', '0.4553', '-0.4724', '-0.4617', '0.4402', '0.503', '0.6255', '0.2832', '0.776', '0.1652', '-0.4302', '-0.483', '-0.1049', '0.6123', '0.004818', '-0.556', '-0.748', '-0.5854', '0.4963', '0.626', '-0.884', '0.3022', '-0.2', '0.5454', '0.9497', '-0.7407', '0.497', '-0.3308', '0.3813', '-0.3562', '-0.1656', '0.3354', '0.9067', '-0.4885', '1.216', '-0.4148', '-0.884', '-0.5522', '-0.3303', '-0.014915', '-0.11835', '0.3555', '-0.532', '-0.1423', '-0.05838', '0.3657', '-0.356', '0.374', '-0.4016', '-0.517', '-0.45', '0.685', '0.68', '-0.3733', '0.05493', '-0.0321', '0.1653']",,,,,,,
mondo:0017949,"ABeta amyloidosis, Arctic type","['cerebral amyloid angiopathy, APP-related, Arctic variant', 'hereditary cerebral hemorrhage with amyloidosis, Arctic type', 'HCHWA, Arctic type', 'hereditary cerebral haemorrhage with amyloidosis, Arctic type', 'ABetaE22G amyloidosis']",,,324723,,"['0.382', '-0.6865', '-0.533', '0.1852', '0.10803', '-0.4214', '-0.7437', '0.525', '-1.498', '0.00229', '-0.1962', '0.1278', '-0.9624', '0.131', '-0.4683', '-0.5503', '0.075', '-0.1946', '-0.1353', '-0.6216', '0.4028', '-0.18', '0.409', '0.0492', '0.1292', '0.614', '-0.4436', '-0.1989', '0.5605', '0.45', '0.2454', '-0.528', '0.817', '-0.733', '0.626', '-0.528', '-0.5557', '0.3013', '0.165', '-0.0961', '0.265', '-0.4363', '-0.2515', '0.3489', '0.358', '-0.503', '-0.562', '0.374', '0.465', '0.8584', '0.275', '0.6665', '0.3247', '-0.4614', '-0.4258', '-0.2072', '0.5', '0.0507', '-0.5156', '-0.7207', '-0.5312', '0.4836', '0.727', '-0.973', '0.1951', '-0.1472', '0.4482', '0.8687', '-0.6987', '0.3733', '-0.341', '0.3584', '-0.4429', '-0.2583', '0.242', '0.912', '-0.4153', '1.327', '-0.5', '-0.8594', '-0.7075', '-0.3174', '-0.05032', '-0.1321', '0.2034', '-0.435', '-0.03238', '0.134', '0.3982', '-0.1842', '0.4368', '-0.3547', '-0.5425', '-0.3748', '0.6426', '0.5566', '-0.37', '-0.2279', '-0.02951', '0.0857']",,,,,,,
mondo:0017950,microcephalic primordial dwarfism,,,,324761,CN437676,,,,,,,,
mondo:0017951,trichorhinophalangeal syndrome,['TRPS'],,,324764,C0265255,,,,,759.89,,,
mondo:0017953,hereditary periodic fever syndrome,['hereditary periodic fever syndrome'],,,324924,CN204099,,,,D056660,,,,
mondo:0017954,pyogenic autoinflammatory syndrome,,,,324927,CN204100,,,,,,,,
mondo:0017955,granulomatous autoinflammatory syndrome,,,,324930,CN204101,,,,,,,,
mondo:0017958,magic syndrome,['mouth and genital ulcers with inflamed cartilage'],,,324972,CN204105,,,,,,,,
mondo:0017961,"46,XX disorder of gonadal development",,,,325055,CN227225,,,,,,,,
mondo:0017962,"46,XX disorder of sex development induced by fetoplacental androgens excess","['46,XX DSD induced by fetoplacental androgens excess']",,,325061,CN227226,,,,,,,,
mondo:0017963,"46,XX disorder of sex development induced by endogenous maternal-derived androgen","['46,XX DSD induced by endogenous maternal-derived androgen']",,,325093,CN227227,,,,,,,,
mondo:0017964,"46,XX disorder of sex development induced by exogenous maternal-derived androgen","['46,XX DSD induced by exogenous maternal-derived androgen']",,,325099,CN227228,,,,,,,,
mondo:0017966,"46,XY disorder of gonadal development",,,,325118,CN227229,,,,,,,,
mondo:0017967,testicular agenesis,"['congenital absence of testes', 'bilateral anorchia', 'absence of testes', 'empty scrotum', 'anorchia']",,,325124,,,,,,,,,
mondo:0017968,"46,XY ovotesticular disorder of sex development","['46,XY ovotesticular DSD']",,,325345,CN227231,,,,,,,,
mondo:0017969,"46,XY disorder of sex development of endocrine origin","['46,XY DSD of endocrine origin']",,,325351,CN227232,,,,,,,,
mondo:0017972,classic congenital lipoid adrenal hyperplasia due to STAR deficency,['classic CLAH'],,,325524,,,,,,,,,
mondo:0017973,non-classic congenital lipoid adrenal hyperplasia due to STAR deficency,,,,325529,,,,,,,,,
mondo:0017974,"46,XY disorder of sex development induced by maternal-exposure to endocrine disruptors","['46,XY DSD induced by maternal-exposure to endocrine disruptors']",,,325537,CN227235,,,,,,,,
mondo:0017975,sex chromosome disorder of sex development,['Sex chromosome DSD'],,,325546,,,,,D058533,,,,
mondo:0017979,autoimmune lymphoproliferative syndrome,"['FAS deficiency', 'autoimmune lymphoproliferative syndrome type 1, autosomal dominant', 'ALPS (autoimmune lymphoproliferative syndrome)', 'ALPS', 'Canale-Smith syndrome']",6688,,3261,C1328840,"['0.2744', '0.0648', '-0.5244', '-0.661', '0.1368', '-0.06586', '-0.1261', '0.312', '-0.0565', '-0.0179', '-0.08484', '-0.02235', '0.2311', '-0.06158', '0.3025', '0.2808', '-0.317', '-0.05927', '-0.3538', '-0.999', '-0.2537', '-0.4053', '0.976', '-0.2932', '0.1279', '0.2637', '-0.008804', '0.234', '-0.1581', '-0.7017', '0.582', '-0.1703', '0.5845', '0.4146', '0.303', '-0.1643', '-0.9185', '-0.147', '-0.4016', '0.01646', '-0.505', '0.2474', '0.5103', '-0.4219', '0.0595', '-0.3547', '-0.1707', '-0.2942', '0.11053', '-0.1103', '-0.07935', '0.2257', '0.2255', '0.06506', '-0.1648', '-0.0224', '-0.5474', '0.1299', '-0.7456', '0.05994', '0.2852', '0.2476', '0.392', '0.00533', '0.1776', '-0.00885', '0.438', '0.4854', '-0.5684', '1.017', '-0.1512', '-0.62', '-0.1294', '0.376', '0.6797', '0.311', '-0.217', '0.10895', '-0.04947', '-0.1248', '0.01758', '-0.05942', '0.001842', '0.0673', '-0.369', '-0.035', '0.764', '0.0473', '0.07623', '-0.2742', '0.7427', '-0.2507', '0.007786', '-0.2412', '0.394', '0.619', '0.2357', '0.2218', '-0.1487', '-0.3809']",C37864,,D056735,279.41,,10069521,
mondo:0017980,syngnathia multiple anomalies,"['syngnathia-multiple anomalies syndrome', 'dobrow syndrome']",,,3262,,,,,,,,,
mondo:0017981,syngnathia-cleft palate syndrome,['syngnathia cleft palate'],,,3263,CN204137,,,,,,,,
mondo:0017983,humero-radio-ulnar synostosis,['humero-radio-ulnar fusion'],,,3266,,,,,,,,,
mondo:0017985,congenital radioulnar synostosis,"['proximal, smooth fusion of 2-6 CM between the radius and ulna and absent head of the radius', 'radio-ulnar synostosis', 'radioulnar synostosis', 'radioulnar synostosis (disease)', 'radio-ulnar synostosis type 1', 'radial-ulnar synostosis', 'radioulnar fusion']",9827,,3269,,,,,C562408,755.53,,,0002974
mondo:0017986,disorder of plasmalogens biosynthesis,['disorder of plasmalogens biosynthesis'],,,3276,CN237437,,,,,,,,
mondo:0017987,syringomyelia,['hydromyelia'],327,,3280,C0039144,,C85179,,D013595,,,10042928,
mondo:0017988,multifocal atrial tachycardia,"['MAT', 'multifocal atrial tachycardia', 'chaotic atrial tachycardia', 'multifocal atrial tachycardia (disease)']",,,3282,C0221158,,,,,427.89,,,0011701
mondo:0017989,His bundle tachycardia,"['JET', 'junctional ectopic tachycardia']",,,3283,C0039235,,C111646,,D013613,427.89,,,
mondo:0017990,catecholaminergic polymorphic ventricular tachycardia,"['stress-induced polymorphic ventricular tachycardia', 'polymorphic catecholergic ventricular tachycardia', 'bidirectional tachycardia induced by catecholamine', 'syncopal paroxysmal tachycardia', 'ventricular tachycardia, catecholaminergic polymorphic', 'CPVT', 'catecholamine-induced polymorphic ventricular tachycardia', 'double tachycardia induced by catecholamines', 'malignant paroxysmal ventricular tachycardia', 'familial polymorphic ventricular tachycardia', 'multifocal ventricular premature beats']",0060674,,3286,C1631597,"['0.7065', '0.612', '0.02159', '0.4175', '-0.364', '-0.6685', '0.3596', '0.9863', '0.3137', '-0.4285', '0.4336', '-0.0865', '0.4668', '0.4106', '-0.1512', '0.01292', '-0.8564', '0.3242', '-0.672', '-0.04678', '0.581', '0.355', '0.8457', '0.05765', '-0.2861', '-0.882', '-0.1919', '0.241', '0.1594', '-0.2124', '0.526', '0.2712', '0.235', '-0.3555', '0.1238', '-0.278', '0.3516', '0.3782', '0.431', '-0.783', '0.2377', '0.3613', '0.5806', '-0.2812', '0.6963', '-0.2048', '-0.902', '-0.06506', '0.1815', '0.2617', '0.1093', '0.3804', '0.04852', '-0.1678', '-0.1924', '0.2397', '-0.1359', '0.4336', '-0.699', '-0.7847', '-0.286', '0.8877', '0.4763', '-0.78', '-0.4553', '0.647', '0.4514', '0.753', '-0.1536', '-0.0342', '-0.1273', '0.6963', '0.1678', '-0.875', '0.3953', '0.555', '0.2429', '-0.1569', '-1.018', '-0.11896', '0.2428', '-0.10065', '0.3303', '-0.08704', '0.1749', '-0.00818', '0.1376', '-0.2069', '1.066', '0.143', '0.02618', '-0.5327', '-0.1704', '0.256', '0.5957', '0.2478', '-0.1418', '-0.359', '-0.9165', '-0.05292']",,,C536334,,I47.2,,
mondo:0017991,Takayasu arteritis,"['aortic arch arteritis', 'aortic arch syndrome', 'Takayasu arteritis', 'Takayasu^s arteritis', 'TA', 'Young female arteritis', 'Takayasu disease', 'Takayasu^s disease', 'pulseless disease', 'idiopathic aortitis', 'cervical aortic arch', 'pharyngeal arch artery syndromic disease']",2508,207600,99079,C0039263,,C35062,1001857,D013625,446.7,,10043097,
mondo:0017992,autoinflammatory syndrome with pyogenic bacterial infection and amylopectinosis,,,,329173,CN237438,,,,,,,,
mondo:0017993,cerebral sinovenous thrombosis,['CSVT'],,,329217,,,,,,,,,
mondo:0017994,severe early-onset obesity-insulin resistance syndrome due to SH2B1 deficiency,,,,329249,CN204200,,,,,,,,
mondo:0017995,spondylocostal dysostosis-hypospadias-intellectual disability syndrome,,,,329252,CN204201,,,,,,,,
mondo:0017997,telecanthus-hypertelorism-strabismus-pes cavus syndrome,,,,3293,CN204205,,,,,,,,
mondo:0017998,PLA2G6-associated neurodegeneration,"['PLA2G6 neurodegeneration with brain iron accumulation', 'PLAN']",,,329303,,,,,,,,,
mondo:0017999,fatty acid hydroxylase-associated neurodegeneration,['FAHN'],,,329308,,,,,C580102,,,,
mondo:0018000,hereditary thrombocytosis with transverse limb defect,"['familial thrombocytosis with transverse limb defect', 'thrombocythemia with distal limb defects']",,,329319,CN204208,,,,,,,,
mondo:0018001,inverse Klippel-Trenaunay syndrome,"['inverse Klippel-Trénaunay syndrome', 'cutaneous hemangioma with muscle or bone atrophy']",,,329324,CN204209,,,,,,,,
mondo:0018002,adult-onset chronic progressive external ophthalmoplegia with mitochondrial myopathy,['adult-onset CPEO with mitochondrial myopathy'],,,329336,C4511138,"['-0.4377', '-0.04138', '-0.16', '-0.4155', '-0.3816', '-0.813', '0.2783', '0.924', '-0.616', '-0.01999', '-0.08234', '-0.1929', '-0.2212', '0.2113', '0.2563', '-0.1713', '-0.02856', '0.03168', '-0.5293', '-0.4648', '0.1722', '-0.3955', '-0.3472', '-0.02278', '-0.139', '-0.1616', '-0.2886', '-0.3118', '-0.1522', '-0.4578', '0.1559', '0.3813', '0.595', '-0.1501', '0.0313', '-0.846', '-0.2957', '-0.223', '-0.3857', '0.1345', '0.0718', '-0.4604', '-0.2527', '0.4949', '-0.1755', '-0.3386', '-0.2139', '0.1112', '-0.083', '0.0886', '-0.2043', '0.5396', '-0.1516', '0.1132', '0.06088', '-0.5986', '0.656', '-0.7227', '-0.2673', '-0.00928', '0.5796', '0.1049', '0.2133', '0.167', '-0.6836', '0.05652', '0.2896', '0.764', '-0.1294', '0.548', '0.0947', '0.2822', '-0.02473', '-0.1423', '0.618', '0.347', '-0.001866', '0.1517', '-0.0857', '0.3213', '0.1678', '0.005447', '0.2312', '0.717', '0.3281', '0.3035', '0.2766', '0.10144', '0.413', '-0.1848', '0.5396', '0.2595', '0.0849', '-0.02179', '0.698', '0.3452', '0.4348', '0.2896', '-0.396', '-0.1366']",,,,,,,
mondo:0018003,limbic encephalitis with DPP6 antibodies,"['limbic encephalitis with dipeptidyl-peptidase 6 antibodies', 'limbic encephalitis with DPPX antibodies']",,,329341,,,,,,,,,
mondo:0018004,acute megakaryoblastic leukemia without down syndrome,['non-DS-AMKL'],,,329469,CN204216,,,,,,,,
mondo:0018005,spastic paraplegia-Paget disease of bone syndrome,,,,329475,CN204217,,,,,,,,
mondo:0018006,adult-onset distal myopathy due to VCP mutation,,,,329478,CN204218,,,,,,,,
mondo:0018007,mosaic genome-wide paternal uniparental disomy,"['genome-wide paternal uniparental disomy mosaicism', 'androgenetic/biparental mosaicism', 'Mosaic genome-wide paternal UPD']",,,329813,CN230278,,,,,,,,
mondo:0018008,idiopathic giant cell myocarditis,['IGCM'],,,329874,,,,,,,,,
mondo:0018009,non-hypoproteinemic hypertrophic gastropathy,['hypertrophic gastropathy without hypoproteinemia'],,,329883,,,,,,,,,
mondo:0018010,juvenile idiopathic inflammatory myopathy,['JIIM'],,,329888,,,,,,,,,
mondo:0018011,juvenile overlap myositis,,,,329894,,,,,,,,,
mondo:0018013,non-immunoglobulin-mediated membranoproliferative glomerulonephritis,"['non-Ig-mediated MPGN', 'C3 glomerulopathy', 'non-immunoglobulin-mediated MPGN', 'non-Ig-mediated membranoproliferative glomerulonephritis']",,,329918,,"['0.9453', '0.3157', '-0.4827', '0.5728', '-0.03009', '-0.606', '0.1951', '-0.02313', '-0.5527', '-0.1967', '0.1764', '-0.1016', '-0.3606', '1.195', '-0.2352', '-0.4207', '-0.3225', '0.599', '0.6274', '-0.1233', '-0.3147', '-0.916', '0.675', '-0.1654', '0.566', '-0.4019', '-0.6953', '0.9053', '0.2568', '-0.1378', '0.1276', '0.2281', '0.771', '0.05298', '-0.0195', '-0.1971', '-0.4607', '0.7393', '0.495', '-0.6904', '-0.6016', '-0.2957', '-0.0696', '-0.4055', '0.318', '-0.2666', '-0.3674', '-0.2411', '-0.2216', '-0.014435', '0.1921', '0.03775', '1.067', '-0.3828', '-0.646', '-0.1289', '-0.000912', '-0.012856', '-0.712', '-0.4707', '-0.884', '0.386', '-0.1841', '-0.04156', '-0.3433', '-0.2421', '0.303', '0.293', '-0.879', '0.583', '-0.8413', '0.1115', '0.369', '-0.343', '-0.0798', '0.2947', '0.578', '1.099', '0.03073', '0.4802', '-0.4248', '0.10144', '-0.01828', '0.002953', '0.312', '-0.0598', '0.2428', '-0.1688', '-0.01187', '1.161', '0.4695', '0.3281', '-0.4634', '0.2352', '0.709', '0.728', '-0.4763', '-0.673', '-0.759', '0.0418']",,,,,,,
mondo:0018014,transient neonatal multiple acyl-CoA dehydrogenase deficiency,"['transient neonatal glutaric aciduria type 2', 'transient neonatal MADD', 'transient neonatal MAD deficiency', 'transient neonatal glutaric acidemia type 2']",,,329942,CN204228,"['-0.505', '0.4436', '-0.2986', '0.1858', '-0.206', '-0.614', '-0.339', '-0.3403', '0.1775', '-0.466', '0.04135', '-0.5654', '0.2084', '0.4612', '-0.4358', '-0.0656', '-0.0775', '-0.2126', '-0.446', '-1.095', '0.3206', '-0.119', '0.4392', '-0.3164', '-0.291', '-0.05063', '-0.5864', '-0.1934', '-0.03418', '-0.4204', '0.5767', '0.3647', '-0.655', '0.4333', '-0.536', '-0.2095', '-0.08215', '-0.2583', '-0.755', '-0.1427', '0.3062', '-0.418', '-0.348', '-0.2457', '0.3901', '-0.6274', '0.2424', '-0.1979', '-0.0828', '0.682', '-0.144', '-0.417', '0.1', '-0.005924', '-0.3552', '-0.7134', '0.437', '0.03018', '-0.2283', '0.4888', '0.662', '0.3572', '0.1504', '0.566', '0.279', '0.4138', '0.479', '-0.275', '-0.8223', '0.455', '0.0014', '-0.3691', '0.3545', '0.11414', '-0.2091', '0.809', '0.001505', '0.05066', '-0.16', '0.12305', '-0.2205', '0.2407', '-0.4731', '-0.11597', '0.6025', '0.663', '-0.1985', '-0.0738', '0.8696', '-0.2482', '0.2678', '0.561', '-0.0761', '-0.3594', '0.287', '0.588', '-0.1382', '0.1209', '0.1006', '-0.1656']",,,,,,,
mondo:0018015,intermittent hydrarthrosis,,,,329967,C0149910,,,,,,M12.4,,
mondo:0018016,classic neuroendocrine tumor of appendix,"['classic appendix neuroendocrine tumor', 'classic appendix neuroendocrine tumour', 'classic appendiceal neuroendocrine tumor', 'classic appendiceal neuroendocrine tumour']",,,329977,CN204231,,,,,,,,
mondo:0018017,goblet cell carcinoma,"['appendix goblet cell carcinoid', 'goblet cell carcinoid', 'mucinous carcinoid tumor', 'goblet cell carcinoma', 'goblet cell tumor', 'mucinous carcinoid', 'appendix goblet cell carcinoid tumour', 'carcinoma of goblet cell', 'goblet cell adenocarcinoid', 'goblet cell carcinoid tumor', 'goblet cell carcinoid tumour', 'appendix adenocarcinoid tumor', 'appendix mixed carcinoid-adenocarcinoma', 'goblet cell tumour', 'appendix goblet cell carcinoid tumor', 'appendix adenocarcinoid tumour', 'GCC', 'mucinous carcinoid tumour']",,,329984,,,C3689,1000090,,,,,
mondo:0018018,wild type ATTR amyloidosis,"['SSA', 'ATTRwt amyloidosis', 'Senile systemic amyloidosis', 'wild type ATTR-related amyloidosis', 'ATTRwt-related amyloidosis']",0080937,,330001,CN204235,,,,,277.39,,,
mondo:0018019,lead poisoning,"['plumbism', 'saturnism', 'Lead intoxication']",,,330015,,,,,D007855,984.9,,,
mondo:0018020,mercury poisoning,"['Mercury toxicity', 'hydrargyria', 'mercurialism', 'Mercury intoxication']",,,330021,,,,1001810,D008630,985.0,,,
mondo:0018021,hypotrichosis-deafness syndrome,,,,330029,CN204237,,,,,,,,
mondo:0018022,hemoglobin Lepore-beta-thalassemia syndrome,"['Lepore-beta-thalassemia syndrome', 'HbLepore-beta-thalassemia syndrome']",,,330032,CN227251,,,,,,,,
mondo:0018023,hemoglobin M disease,"['hereditary methemoglobinemia due to hemoglobin mutation', 'M hemoglobinopathy', 'autosomal dominant methemoglobinemia', 'methemoglobinemia, beta-globin type', 'methemoglobinemia, beta type', 'hereditary methemoglobinemia due to haemoglobin mutation', 'blue baby syndrome']",,617971,330041,CN204238,,,,C581942,,,,
mondo:0018024,hydroa vacciniforme,['hV'],,,330058,C0020241,,C84766,,D006837,,,,
mondo:0018025,chronic actinic dermatitis,"['actinic reticuloid', 'chronic photosensitivity dermatitis']",,,330064,C1510437,,,,,692.73,,,
mondo:0018026,tetraploidy syndrome,,,,3305,C0795884,,,,D057891,,,,
mondo:0018027,duplication/inversion 15q11,"['duplication/inversion 15q11', 'Inv dup(15)', 'Isodicentric 15 chromosome', 'non-distal tetrasomy 15q', 'non-telomeric tetrasomy 15q', 'Invdup(15)', 'inverted duplication 15', 'Isodicentric chromosome 15 syndrome', 'Duplication/inversion type 15q11', 'tetrasomy 15q', 'idic(15)', 'chromosome 15q tetrasomy']",,,3306,,,,,C580205,,,,
mondo:0018028,tetrasomy 5p,"['Isochromosome 5p', 'tetrasomy type 5p']",,,3309,,,,,,,,,
mondo:0018029,congenital factor XIII deficiency,"['factor XIII deficiency disease', 'hereditary factor XIII deficiency disease', 'deficiency, Laki-Lorand factor', 'fibrin-stabilizing factor deficiency', 'fibrin stabilising factor deficiency', 'fibrin stabilizing factor deficiency', 'factor XIII deficiency']",2211,,331,,"['0.358', '-0.399', '-0.8047', '-0.286', '0.099', '0.2683', '-0.08984', '0.6743', '-0.2751', '-0.1337', '-0.1091', '-0.1866', '-0.06223', '-0.08545', '0.1189', '-0.1209', '0.1372', '-0.1342', '-0.468', '-1.178', '-0.2524', '-0.417', '1.1045', '-0.166', '0.02803', '-0.2153', '-0.3064', '0.1918', '0.5825', '0.05652', '0.0599', '0.2369', '0.6597', '0.3838', '-0.1057', '-0.1719', '0.2054', '-0.523', '0.2499', '-0.0847', '0.3481', '0.1075', '-0.0567', '-0.2461', '0.707', '0.4182', '-0.1301', '0.1597', '0.4214', '0.5903', '0.5103', '-0.3618', '0.2734', '0.127', '-0.395', '-0.1194', '0.1669', '-0.3286', '-0.632', '0.394', '-0.3516', '0.2815', '0.413', '-0.2032', '0.444', '-0.169', '0.2236', '0.3047', '0.1007', '0.1112', '-0.7407', '-0.1831', '-0.8228', '-0.917', '0.9277', '-0.2615', '0.935', '0.0418', '-0.05615', '-0.1295', '-0.7754', '-0.0871', '-0.02293', '-0.2283', '-0.1978', '-0.0895', '0.458', '0.3132', '-0.05295', '-0.6147', '-0.00733', '0.8237', '-0.006298', '-0.05264', '0.6367', '0.917', '-0.02866', '-0.6836', '0.1709', '-0.2776']",C131633,,,286.3,,,
mondo:0018030,tetrasomy 9p,"['Isochromosome 9p', 'tetrasomy type 9p', 'tetrasomy of short arm of chromosome 9', 'Mosaic tetrasomy 9p', 'chromosome 9p tetrasomy']",,,3310,C0795832,,,,C538027,,,,
mondo:0018031,granulomatous slack skin disease,,,,33111,C0376407,,C35464,,,,C84.0,,
mondo:0018034,thalidomide embryopathy,"['thalidomide embryopathy syndrome', 'foetal thalidomide syndrome', 'fetal thalidomide syndrome', 'thalidomide-induced birth defect']",,,3312,C0432365,,C99082,,,759.89,,10071249,
mondo:0018037,hyper-IgE syndrome,"['HIES', 'hyperimmunoglobulin E syndrome', 'hyper-IgE recurrent infection syndrome']",0080545,,331223,CN204280,"['0.06744', '0.03787', '-0.0994', '-0.277', '-0.02289', '-0.44', '0.1606', '-0.1288', '-0.09766', '0.0719', '0.03928', '0.11194', '-0.2386', '-0.10077', '-0.1006', '0.0831', '-0.0547', '0.2131', '-0.05957', '-0.6865', '-0.1052', '-0.1831', '0.3696', '0.08057', '0.1196', '0.0106', '-0.1129', '-0.1298', '0.1118', '-0.4307', '0.304', '0.2206', '0.03925', '0.197', '0.0861', '0.01932', '-0.234', '-0.09784', '0.0332', '-0.2194', '0.2325', '-0.407', '0.0922', '0.0428', '0.0547', '-0.1741', '-0.0986', '0.1322', '0.08105', '-0.184', '-0.10474', '-0.04163', '0.1532', '0.01209', '-0.2927', '-0.2413', '0.08105', '-0.1697', '0.04144', '0.06964', '0.4617', '0.02458', '0.04553', '-0.076', '0.3665', '-0.08826', '0.2272', '0.04938', '-0.3516', '0.3047', '-0.2461', '-0.2079', '-0.2422', '-0.1033', '0.2434', '0.128', '0.1594', '0.1975', '0.1671', '0.02823', '-0.126', '-0.042', '-0.05884', '0.1885', '-0.07355', '0.10474', '0.11896', '0.11414', '0.09015', '0.08673', '0.1884', '0.3303', '0.06946', '-0.0923', '0.585', '0.4197', '0.4954', '-0.382', '-0.2311', '-0.0668']",C3144,,,,,,
mondo:0018039,selective IgM deficiency,"['selective immunoglobulin M deficiency', 'selective IgM deficiency disease', 'SIgMD']",0050222,,331235,,,,,,279.02,,,
mondo:0018043,Thomas syndrome,['Potter sequence-cleft lip/palate-cardiopathy syndrome'],,,3316,C2931225,,,,C536514,,,,
mondo:0018044,idiopathic hypersomnia,"['primary hypersomnia', 'idiopathic hypersomnolence']",,,33208,C0751757,,C116343,,D020177,,,,
mondo:0018045,Hoyeraal-Hreidarsson syndrome,"['progressive pancytopenia-immunodeficiency-cerebellar hypoplasia syndrome', 'Hoyeraal Hreidarsson syndrome', 'Growth retardation prenatal with progressive pancytopenia and cerebellar hypoplasia']",,,3322,C1846142,,,,C536068,,,,
mondo:0018046,thrombocytopenia-Robin sequence syndrome,"['congenital thrombocytopenia, Robin sequence, agenesis of the corpus callosum, distinctive facies and developmental delay', 'thrombocytopenia Robin sequence', 'Braddock Carey syndrome']",,,3323,C2931364,,,,C536898,,,,
mondo:0018047,familial thrombomodulin anomalies,"['thrombomodulin anomalies, familial']",,,3324,C2931365,,,,C536900,,,,
mondo:0018048,heparin-induced thrombocytopenia,"['HAT', 'heparin-induced thrombocytopenia', 'heparin-induced thrombocytopenia (disease)', 'heparin-induced thrombocytopenia type 2', 'HIT', 'heparin-associated thrombocytopenia']",,,3325,C0272285,,,,,289.84,,10062506,0011874
mondo:0018050,tibial aplasia-ectrodactyly syndrome,"['tibial hemimelia-ectrodactyly syndrome', 'ectrodactyly with aplasia of long bones', 'TH-SHFM', 'aplasia of tibia with ectrodactyly', 'split-hand/foot malformation with long bone deficiency', 'split hand/foot malformation with long bone deficiency', 'tibial hemimelia with split hand/foot malformation', 'SHFM associated with aplasia of long bones', 'aplasia of tibia with split-hand/split-foot deformity', 'split-hand/foot malformation associated with aplasia of long bones', 'SHFLD syndrome', 'SHFLD', 'tibial aplasia with split-hand/split-foot deformity']",,,3329,,"['-0.0878', '0.1862', '0.3474', '-0.398', '0.1185', '-0.2905', '0.11523', '0.4868', '-0.4597', '-0.507', '-0.3367', '0.1311', '-0.2136', '-0.2316', '0.0417', '-0.06476', '0.0946', '-0.3904', '0.1475', '-0.512', '-0.0438', '0.08563', '0.6885', '-0.0856', '0.2712', '0.2191', '-0.1321', '0.1387', '0.652', '-0.4033', '0.5537', '-0.1718', '-0.08923', '0.3486', '0.2576', '-0.2377', '-0.11914', '-0.4006', '-0.08276', '-0.3862', '-0.2854', '-0.1663', '-0.0445', '-0.2411', '-0.1445', '-0.2522', '-0.0872', '0.303', '-0.06052', '-0.11707', '-0.1046', '-0.2479', '-0.3176', '-0.3955', '-0.5444', '-0.1777', '0.0962', '-0.315', '-0.3582', '-0.12445', '-0.1559', '-0.006294', '-0.277', '0.331', '-0.1791', '0.224', '0.223', '0.293', '-0.4412', '0.1081', '-0.4248', '0.04257', '0.2428', '-0.2532', '0.3286', '0.00223', '0.1451', '-0.1663', '-0.1315', '-0.8545', '-0.03745', '-0.1423', '0.3687', '0.526', '0.02876', '-0.01701', '-0.5986', '0.3677', '-0.09717', '-0.3154', '0.08746', '0.3113', '0.3328', '0.0701', '0.513', '-0.441', '0.4575', '-0.5713', '0.03473', '0.1553']",,,,,,,
mondo:0018051,Jessner lymphocytic infiltration of the skin,"['Jessner disease', 'benign chronic T-cell infiltrative disorder', 'Jessner-Kanof lymphocytic infiltration of the skin', 'Jessner-Kanof syndrome', 'lymphocytic infiltrate of Jessner', 'benign lymphocytic infiltration']",,,33314,C0580181,,,,,,,,
mondo:0018053,trichothiodystrophy,['trichothiodystrophy syndrome'],0111866,,33364,C1955934,"['-0.2457', '0.2747', '0.0367', '-0.336', '0.818', '-0.4336', '-0.3455', '0.11804', '-0.375', '-0.2703', '0.3838', '0.1512', '-0.007637', '0.1853', '0.273', '0.396', '0.4326', '-0.263', '-0.5303', '-0.735', '-0.1184', '-0.1958', '0.7695', '0.03802', '0.5737', '0.1277', '-0.5864', '-0.4058', '0.1512', '-0.558', '0.3484', '0.02592', '-0.0711', '0.1848', '-0.010925', '-0.03018', '-0.3987', '-0.1711', '-0.4978', '-0.1931', '0.488', '-0.2803', '-0.03415', '0.11304', '0.3613', '-1.012', '0.4731', '0.03217', '0.4893', '-0.4475', '-0.2194', '-0.285', '0.1569', '0.06128', '-0.2617', '-0.258', '0.2468', '-0.004795', '-0.545', '0.3455', '0.0875', '-0.3843', '0.3308', '0.04776', '0.399', '0.0641', '0.05942', '-0.0289', '-0.525', '0.3037', '-0.6445', '-0.01741', '-0.0484', '0.2827', '0.4243', '-0.092', '0.004795', '-0.0758', '-0.02887', '-0.2484', '0.398', '-0.149', '-0.4546', '-0.2369', '-0.586', '-0.4792', '-0.05905', '0.4312', '0.2954', '0.4187', '0.0846', '0.2363', '-0.3882', '-0.2347', '0.1609', '0.02666', '0.10895', '-0.3218', '0.06885', '0.2162']",C4924,,,,,10044628,
mondo:0018054,familial atrial fibrillation,"['autosomal dominant atrial fibrillation', 'atrial fibrillation, familial', 'atrial fibrillation autosomal dominant', 'hereditary atrial fibrillation (disease)', 'ATFB']",0050650,,334,CN204347,,,,,,,,
mondo:0018055,pediatric hepatocellular carcinoma,"['childhood carcinoma of liver cell', 'paediatric hepatoma', 'childhood-onset hepatocellular carcinoma', 'Pediatric carcinoma of the liver cell', 'paediatric HCC', 'childhood liver cell carcinoma', 'paediatric liver cell carcinoma', 'childhood hepatoma', 'paediatric carcinoma of liver cell', 'pediatric carcinoma of liver cell', 'pediatric hepatoma', 'pediatric HCC', 'hepatocellular cancer', 'Paediatric carcinoma of the liver cell', 'pediatric liver cell carcinoma', 'childhood hepatocellular carcinoma', 'childhood-onset HCC', 'childhood carcinoma of the liver cell']",0070322,,33402,CN204349,,C7955,,,,,,
mondo:0018056,bullous lichen planus,,,,33408,C0023648,,C34778,,,,L43.1,10056960,
mondo:0018058,tracheal agenesis,"['congenital tracheal agenesis', 'tracheal absence', 'congenital absence of trachea']",,,3346,C1261567,,C35376,,C536975,,,,
mondo:0018059,meningococcal meningitis,,0080176,,33475,C0025294,,,1001040,D008585,036.0,A39.0,10027276,
mondo:0018060,congenital fibrinogen deficiency,"['fibrinogen deficiency, congenital']",,,335,,"['-0.282', '-0.1318', '-0.8477', '-0.3254', '0.1117', '0.2952', '0.3845', '0.3982', '-0.2935', '-0.00787', '-0.5615', '0.2605', '-0.222', '0.717', '-0.1475', '-0.4287', '-0.4375', '-0.2131', '-0.5103', '-0.6875', '-0.8804', '0.4402', '0.9014', '-0.3914', '0.2053', '-0.0503', '0.1952', '-0.2896', '-0.1974', '0.10657', '-0.2294', '0.3313', '0.8604', '0.8364', '-0.1209', '-0.4087', '-0.5127', '-0.8477', '-0.2097', '-0.08014', '0.419', '0.00787', '0.2229', '-0.4688', '0.4348', '0.12335', '-0.1747', '0.4841', '0.2974', '0.6226', '0.7954', '-0.5205', '0.06964', '-0.349', '-0.847', '0.878', '0.3665', '-0.2358', '-0.126', '0.3699', '-0.5938', '0.22', '0.2559', '-0.2637', '0.03134', '0.2861', '0.259', '0.193', '-0.05927', '0.3433', '0.10266', '-0.04932', '-0.849', '-0.707', '1.016', '0.00488', '1.211', '-0.4514', '-0.0747', '-0.07477', '-0.4497', '-0.1694', '-0.02644', '-0.008644', '0.104', '0.1462', '-0.01672', '0.4783', '0.4158', '-0.6543', '0.5283', '0.9707', '0.07056', '0.2732', '0.6694', '0.1014', '0.634', '-0.657', '-0.106', '0.726']",,,,,,,
mondo:0018061,trichodermodysplasia-dental alterations syndrome,"['Pinheiro-Freire Maia-Miranda syndrome', 'Trichodermodysplasia with dental alterations', 'Pinheiro Freire-Maia Miranda syndrome']",,,3353,C2931485,,,,C537402,,,,
mondo:0018062,autosomal dominant trichoodontoonychodysplasia-syndactyly,"['ectodermal dysplasia with corkscrew hairs', 'Tricho-odonto-onychodysplasia with syndactyly', 'Trueb Burg Bottani syndrome', 'Trueb-Burg-Bottani syndrome']",,,3357,C2931239,,,,C536565,,,,
mondo:0018063,nodular non-suppurative panniculitis,"['Weber-Christian panniculitis', 'Weber - Christian disease', 'WCD', 'nodular non-suppurative febrile panniculitis', 'Pfeiffer-Weber-Christian syndrome', 'idiopathic nodular panniculitis', 'panniculitis nodular nonsuppurative', 'Relapsing febrile nodular panniculitis', 'Relapsing febrile nodular nonsuppurative panniculitis', 'nodular nonsuppurative panniculitis', 'idiopathic lobular panniculitis', 'Weber Christian disease', 'Weber-Christian disease']",1525,,33577,C0030328,,,1000742,D010201,,,10047883,
mondo:0018064,trigonocephaly-broad thumbs syndrome,"['Hunter-Rudd-Hoffmann syndrome', 'Hunter Rudd Hoffmann syndrome']",,,3365,,,,,,,,,
mondo:0018065,isolated trigonocephaly,"['non-syndromic metopic craniosynostosis', 'nonsyndromic trigonocephaly']",,,3366,CN239481,"['-0.06244', '-0.06915', '-0.2451', '-0.2905', '0.3735', '0.0003405', '0.3677', '0.667', '-1.118', '-0.159', '0.05402', '0.08276', '0.3298', '-0.1991', '0.005093', '-0.1268', '0.497', '-0.1885', '-0.4263', '-0.2827', '-0.3652', '-0.1024', '1.063', '-0.374', '0.6675', '-0.03592', '-0.0756', '-0.1559', '-0.2264', '0.2118', '0.295', '0.0806', '0.3428', '0.12225', '0.2383', '-0.02696', '0.1836', '-0.3765', '0.05164', '-0.619', '0.4834', '-0.1333', '0.3152', '-0.616', '0.1688', '-0.0982', '-0.2986', '0.0316', '-0.2183', '-0.04053', '0.537', '-1.0625', '0.1943', '0.2423', '-0.4614', '0.318', '0.3677', '0.00262', '0.2097', '0.04816', '0.128', '0.01752', '0.01965', '0.2023', '-0.2024', '-0.4636', '0.4124', '0.4133', '-0.294', '0.136', '0.03745', '0.4062', '0.3247', '-0.2903', '-0.744', '0.404', '0.1131', '-0.1832', '-0.7017', '-0.585', '-0.1121', '-0.005405', '-0.3557', '0.6753', '-0.1255', '0.02621', '-0.3892', '-0.3677', '0.10333', '-0.276', '-0.1947', '0.194', '-0.233', '0.522', '0.7437', '-0.0383', '0.562', '-0.564', '0.2844', '-0.6533']",,,,,,,
mondo:0018066,trisomy X,"['XXX syndrome', '47 XXX syndrome', 'triple-X chromosome syndrome', '47,XXX syndrome', 'Triplo-X syndrome', 'trisomy type X', 'triple-X female', 'trisomy X', '47,XXX', 'triple X syndrome', 'Triplo X syndrome']",,,3375,C0221033,,C129718,,C535318,,,,
mondo:0018067,triploidy,"['triploid syndrome', 'chromosome triploidy syndrome', 'triploidy syndrome']",,,3376,C0333693,,C85204,,D057885,758.89,,,
mondo:0018068,trisomy 13,"['trisomy type 13', 'trisomy 13', 'Patau^s syndrome', 'D1 trisomy', 'Patau syndrome', 'D trisomy syndrome (formerly)', 'chromosome 13, trisomy 13 complete']",11665,,3378,CN204386,,C36529,,C536305,758.1,,10044686,
mondo:0018069,distal trisomy 17q,"['trisomy 17qter', 'telomeric duplication 17q', 'distal trisomy type 17q', 'distal duplication 17q']",,,3379,,,,,,,,,
mondo:0018070,familial multiple fibrofolliculoma,['multiple fibrofolliculoma familial'],,,338,CN204388,,,,,,,,
mondo:0018071,trisomy 18,"['chromosome 18 duplication', 'complete trisomy 18 syndrome', '18 trisomy', 'trisomy type 18', 'chromosome 18 trisomy', 'Edwards syndrome', 'E3 trisomy', 'trisomy 18', 'trisomy E (formerly)', 'trisomy 16-18 (formerly)']",1085,,3380,C0152096,,C36626,,C580500,758.2,,10053884,
mondo:0018072,persistent truncus arteriosus,"['persistent truncus arteriosus', 'common truncus arteriosus', 'truncus arteriosus', 'common arterial trunk', 'persistent truncus arteriosus (disease)', 'TAC', 'common aorticopulmonary trunk']",,,3384,,,C98880,,D014339,,,,
mondo:0018075,neural tube defect,"['spinal dysraphism', 'NTD']",0080074,,3388,,,C84923,,D009436,742.8,,,
mondo:0018076,tuberculosis,"['Kochs disease', 'TB', 'active tuberculosis', 'tuberculosis disease']",399,,3389,C0151332,"['0.744', '0.4297', '-0.4226', '0.3357', '-0.03723', '-0.05978', '0.535', '0.4465', '0.02554', '-0.2222', '-0.353', '0.298', '-0.472', '0.67', '-0.548', '-0.2072', '-1.164', '0.05527', '-0.806', '-0.5347', '-0.303', '-0.5664', '0.6987', '-0.1527', '-0.1451', '-0.1603', '-0.3425', '0.298', '0.23', '0.1619', '0.6826', '-0.1919', '0.1315', '0.13', '0.2976', '-0.09894', '-0.6343', '-0.12036', '0.4954', '-0.2588', '-0.4739', '-0.2263', '0.1877', '-0.61', '0.1464', '0.3093', '-0.1534', '-0.2346', '0.1317', '1.028', '-0.0524', '-0.0487', '0.5776', '-0.2023', '-0.02028', '0.3281', '-0.01851', '0.565', '-0.36', '-0.5093', '-0.0932', '0.2617', '-0.5444', '0.2688', '-0.396', '-0.0388', '0.374', '-0.0495', '-0.858', '0.8984', '-0.032', '-0.144', '0.2864', '-0.288', '0.4287', '0.539', '-0.3826', '0.3804', '0.2993', '0.2505', '-0.8164', '-0.25', '-0.1274', '0.523', '0.272', '0.4392', '0.726', '0.295', '0.0919', '0.3225', '0.597', '-0.434', '-0.01845', '-0.002338', '0.623', '0.867', '-0.5737', '-0.4666', '0.0765', '-0.637']",C3423,,D014376,017.96,A15-A19,10044755,
mondo:0018077,tularemia,"['Pahvant Valley plague', 'Ohara disease', 'lemming fever', 'Deerfly fever', 'rabbit fever', 'Yatobyo (Japan)', 'Francisella tularensis caused disease or disorder', 'Francisella tularensis infection']",2123,,3392,C0041351,,C85208,1001444,D014406,021.9,A21,10045146,
mondo:0018078,soft tissue sarcoma,"['malignant mesenchymal tumour', 'non-Rhabdo. soft tissue sarcoma', 'malignant soft tissue tumor', 'malignant mesenchymal tumor', 'malignant soft tissue tumour', 'connective tissue sarcoma', 'sarcoma of soft tissue', 'soft part sarcoma', 'sarcoma of the soft tissue', 'soft tissue sarcoma']",,,3394,CN204398,,C9306,1001968,,,,,
mondo:0018079,thymic epithelial neoplasm,"['Thymus epithelial tumour', 'thymic epithelium neoplasm', 'thymoma, adult', 'epithelial tumour of the Thymus', 'thymus epithelial neoplasm', 'epithelial tumor of the Thymus', 'epithelial neoplasm of Thymus', 'Thymus epithelial tumor', 'epithelial tumor of Thymus', 'thymic epithelial tumor', 'Tet', 'thymic epithelial tumour', 'Thymus epithelial neoplasm', 'epithelial tumour of Thymus', 'epithelial neoplasm of the Thymus', 'TEN']",,,3398,C1266101,,C6450,,C536905,,D15.0,,
mondo:0018081,hemorrhagic fever-renal syndrome,"['Hantavirus fever', 'Hantavirosis']",,,340,CN204401,,,,C535630,,,10023484,
mondo:0018082,aorto-ventricular tunnel,"['aorto-ventricular tunnel (disease)', 'aorto-ventricular tunnel']",,,3400,CN225932,,,,D000082903,,,,0011627
mondo:0018083,transient tyrosinemia of the newborn,"['transient tyrosinemia of the neonate', 'tyrosine-oxidase temporary deficiency', 'transient neonatal tyrosinemia']",,,3402,CN204402,,,,,,,,
mondo:0018084,Uhl anomaly,"['parchment right ventricle', 'Uhl^s anomaly']",,,3403,,,,,C536932,,,10048951,
mondo:0018085,umbilical cord ulceration-intestinal atresia syndrome,"['umbilical cord ulcer with intestinal atresia', 'umbilical cord ulceration and intestinal atresia', 'umbilical ulceration and intestinal atresia']",,,3405,C2931371,,,,C536938,,,,
mondo:0018086,ulerythema ophryogenesis,"['type of genodermatosis', 'keratosis pilaris affecting the follicles of the eyebrow hairs']",,,3406,,"['0.2507', '0.05972', '-0.2471', '-0.0526', '0.1469', '-0.3914', '0.1573', '0.3484', '-0.3274', '0.162', '0.2291', '0.0713', '-0.1497', '0.2391', '0.2183', '0.2056', '0.453', '-0.4604', '-0.10626', '-0.2279', '-0.3223', '-0.345', '0.2358', '-0.1315', '0.2145', '0.00085', '-0.5903', '0.153', '-0.3965', '0.002598', '0.4355', '-0.4028', '-0.06128', '-0.3', '0.3372', '0.2201', '-0.05753', '-0.3745', '0.05438', '0.01365', '0.2418', '-0.1941', '0.0808', '-0.227', '0.1034', '-0.1149', '-0.1385', '0.1797', '-3.207e-05', '0.1119', '-0.04807', '-0.2532', '0.2415', '0.2756', '-0.2812', '-0.001532', '0.4067', '0.1335', '-0.375', '-0.0818', '0.006287', '0.09656', '-0.2532', '-0.2119', '0.04498', '0.226', '0.2272', '0.6104', '0.428', '0.653', '-0.3218', '-0.304', '0.3008', '-0.1543', '-0.0594', '0.2228', '-0.1036', '-0.257', '0.2109', '-0.4233', '0.0954', '-0.3738', '0.2355', '0.1575', '-0.06805', '-0.08295', '-0.3867', '0.2793', '0.11865', '0.383', '0.1842', '0.246', '-0.0796', '0.1755', '0.4587', '-0.0687', '0.5454', '-0.4385', '0.173', '-0.0947']",,,,,,,
mondo:0018087,viral hemorrhagic fever,"['viral haemorrhagic fever', 'haemorrhagic fever', 'VHFs', 'VHF', 'hemorrhagic fevers', 'hemorrhagic fever', 'haemorrhagic fevers, viral']",,,341,CN204409,,C36170,,D006482,,,,
mondo:0018088,familial Mediterranean fever,"['familial paroxysmal polyserositis', 'FMF', 'benign paroxysmal peritonitis', 'periodic disease', 'benign recurrent polyserositis']",2987,,342,C0031069,"['0.1536', '-0.003704', '-1.102', '-0.3276', '-0.10004', '-0.3447', '-0.2003', '0.519', '-0.602', '-0.5933', '-0.3306', '0.518', '-0.2795', '0.7173', '-0.8555', '-0.1675', '-0.5986', '0.05228', '0.4368', '-0.5137', '0.2537', '0.03964', '0.455', '-0.4128', '-0.1084', '0.2786', '0.04852', '0.1082', '0.1495', '-0.64', '0.7236', '-0.6157', '0.4395', '-0.3022', '0.11786', '-0.447', '-0.3572', '-0.1873', '0.1989', '-0.1279', '0.1979', '-0.616', '0.3206', '-0.121', '0.2168', '-0.08594', '-0.2705', '-0.02208', '0.2017', '0.531', '-0.678', '0.1439', '0.557', '0.2109', '0.5776', '-0.10095', '0.456', '0.327', '0.1476', '-0.1965', '0.2477', '0.3389', '-0.0366', '-0.4075', '0.4385', '-0.1143', '-0.0638', '0.2236', '-0.3025', '0.2401', '0.05606', '0.1041', '-0.1924', '-0.2712', '-0.1583', '0.851', '0.0265', '0.6167', '0.2358', '0.0006013', '0.003849', '-0.2893', '-0.04297', '-0.653', '0.465', '-0.1858', '0.4202', '0.4114', '-0.0926', '0.26', '0.2983', '0.02696', '-0.1904', '-0.2402', '0.324', '0.2194', '-0.2588', '-0.3809', '-0.3003', '-0.371']",C84707,,D010505,277.31,,10016207,
mondo:0018089,double outlet right ventricle,"['Dextrotransposition of aorta', 'double outlet right ventricle', 'DORV']",6406,,3426,C0013069,"['-0.7764', '-0.2708', '0.05966', '0.4204', '0.913', '-0.4077', '0.4775', '0.1498', '-0.3137', '0.1425', '-0.579', '-0.8413', '0.10004', '0.59', '-0.0387', '-0.2062', '-0.766', '-0.752', '-0.3643', '-0.7007', '-0.04926', '1.144', '1.254', '-0.3901', '0.2935', '-0.06335', '0.0772', '0.4087', '0.3833', '0.1486', '0.81', '0.1742', '0.0827', '0.03528', '0.10596', '0.08594', '0.012215', '0.4368', '0.1882', '0.1152', '0.669', '0.47', '0.7837', '0.2173', '0.4246', '0.1045', '-0.4683', '0.11505', '-0.3098', '-0.2463', '-0.2421', '-0.215', '-0.1593', '-0.5747', '-0.632', '0.03406', '0.2383', '0.1495', '-0.4932', '-0.0371', '-0.282', '0.362', '0.3774', '0.2795', '0.1309', '0.10266', '0.8037', '0.1705', '0.0902', '0.59', '-0.182', '0.0708', '0.2686', '-0.3726', '0.2966', '0.2281', '0.1663', '-0.5205', '-0.4978', '-0.527', '0.0958', '0.226', '0.4382', '0.2688', '0.1131', '0.1093', '0.661', '0.397', '-0.1505', '-0.4514', '-0.4758', '0.0903', '-0.3777', '-0.08856', '1.023', '0.1893', '0.4124', '-0.642', '-0.2522', '-0.1667']",C98916,,D004310,,Q20.1,10013611,
mondo:0018090,double outlet left ventricle,"['DOLV', 'double outlet left ventricle (disease)', 'Double outlet left ventricle']",,,3427,,,,,,745.19,,,0011581
mondo:0018091,microcephaly-brachydactyly-kyphoscoliosis syndrome,"['microcephaly brachydactyly kyphoscoliosis', 'microcephaly, short stature, brachydactyly type D, flattened occiput, low-set large ears, prominent nose, kyphoscoliosis and intellectual disability', 'Viljoen Kallis Voges syndrome', 'Viljoen-Kallis-Voges syndrome']",,,3433,C2931177,,,,C536349,,,,
mondo:0018092,Vogt-Koyanagi-Harada disease,"['uveomeningoencephalitic syndrome', 'VKH disease', 'Uveomenigitic syndrome', 'Harada^s disease', 'Vogt-Koyanagi syndrome', 'Vogt-Koyanagi-Harada syndrome', 'VKH syndrome']",12297,,3437,C0042170,,C85218,,D014607,364.24,,,
mondo:0018093,arbovirus fever,"['Arbovirosis', 'arbovirus fever']",,,344,CN227261,,,,,,,,
mondo:0018094,Waardenburg syndrome,"['Waardenburg, types I and/or II', 'van der Hoeve Halbertsona Waardenburg syndrome', 'Waardenburg syndrome', 'Waardenburg^s syndrome', 'Van der Hoeve Halbertsma Waardenburg Gualdi syndrome', 'Waardenburg Shah syndrome', 'Mende syndrome']",9258,,3440,,"['0.699', '0.137', '-0.2363', '0.2092', '0.7085', '-0.2252', '0.2151', '0.4604', '-0.1792', '0.0849', '-0.2544', '-0.3928', '-0.2617', '0.1635', '-0.3196', '0.1777', '0.2074', '-0.4836', '-0.1936', '-0.0748', '-0.4028', '0.04684', '0.9336', '-0.5186', '0.2507', '-0.05276', '-0.1215', '0.2896', '0.9766', '-0.558', '1.043', '0.02669', '-0.1074', '0.4739', '0.2091', '0.0597', '-0.9126', '0.04874', '-0.3474', '0.09985', '0.543', '-0.4844', '0.494', '-0.3708', '-0.1307', '-0.852', '0.391', '0.529', '-0.2418', '-0.467', '0.2463', '-0.652', '-0.5303', '-0.3313', '0.03418', '-0.5737', '0.24', '-0.05496', '-0.3179', '-0.3892', '-0.784', '-0.568', '0.02982', '0.331', '-0.3127', '0.1682', '0.2441', '0.5386', '-0.6494', '0.4485', '-0.234', '0.1117', '0.2015', '-0.02171', '0.653', '0.04407', '-0.241', '-0.4448', '-0.1702', '-0.4119', '0.565', '-0.3245', '-0.2625', '0.4902', '-0.02782', '-0.483', '0.5', '0.807', '0.1946', '-0.2073', '0.2546', '1.186', '0.483', '0.3584', '0.865', '-0.818', '0.1672', '-0.4683', '-0.6055', '0.01654']",C85222,,D014849,,E70.3,10069203,
mondo:0018095,Weaver-Williams syndrome,,,,3448,CN204431,,,,,,,,
mondo:0018096,Weill-Marchesani syndrome,"['spherophakia brachymorphia syndrome', 'mesodermal Dysmorphodystrophy, congenital', 'mesodermal dysmorphodystrophy congenital', 'congenital mesodermal dystrophy', 'WM syndrome', 'spherophakia-brachymorphia syndrome', 'Marchesani-Weill syndrome', 'WMS']",0050475,,3449,C0265313,"['-0.2756', '-0.02077', '0.318', '-0.393', '0.405', '-0.4106', '0.2612', '0.908', '-0.4614', '-0.588', '-0.342', '-0.3943', '-0.04834', '0.2401', '-0.2854', '-0.1458', '0.3599', '-0.258', '0.08905', '-0.54', '-0.132', '0.535', '0.2267', '0.19', '-0.07526', '0.2489', '0.013214', '0.473', '0.4675', '0.1685', '0.4521', '-0.3083', '0.6455', '0.2578', '-0.2288', '-0.2986', '0.1096', '-0.277', '-0.005657', '-0.2051', '0.2375', '0.04398', '0.596', '0.4963', '0.1589', '0.6284', '0.11743', '0.406', '-0.1562', '-0.2056', '0.03802', '0.1653', '-0.1974', '-0.3186', '-0.0449', '-0.659', '0.1957', '0.08185', '0.0839', '0.04034', '0.839', '0.02364', '-0.497', '0.214', '0.05682', '-0.2406', '0.0778', '0.3137', '-0.4973', '-0.3376', '-0.678', '0.06464', '-0.1079', '-0.3997', '0.337', '0.1277', '-0.0952', '-0.4758', '-0.4316', '0.1471', '0.1609', '-0.0504', '-0.3394', '0.2542', '-0.517', '0.2487', '0.3503', '0.5884', '0.02713', '0.3801', '-0.1584', '-0.1208', '-0.3936', '-0.2118', '1.279', '0.052', '0.59', '-0.2432', '0.04965', '-0.05685']",C85226,,D056846,759.89,,10064963,
mondo:0018097,West syndrome,"['West^s syndrome', 'Infantile spasms syndrome', 'infantile spasms', 'tonic spasms with clustering, arrest of psychomotor development and hypsarrhythmia on EEG', 'X-linked infantile spasms', 'intellectual disability-hypsarrhythmia syndrome', 'X-linked infantile spasm syndrome']",0050562,,3451,C0037769,"['0.7534', '0.1865', '-0.42', '-0.5605', '-0.10956', '-0.925', '1.181', '0.75', '-0.6675', '-0.3315', '-0.1465', '0.1461', '-0.09485', '0.4016', '0.09296', '0.2817', '-0.1626', '-0.4763', '-0.1401', '-0.7954', '0.292', '-0.4766', '0.473', '-0.3945', '0.02902', '-0.2688', '-0.05673', '-0.3398', '-0.1763', '0.4583', '0.2229', '0.536', '0.11383', '-0.2979', '-0.3428', '0.6685', '0.4028', '-0.3574', '-0.1055', '0.1827', '0.304', '-0.595', '-0.4666', '0.0889', '0.7764', '0.08484', '-0.9146', '0.5986', '-0.03806', '0.2302', '0.3308', '-0.1438', '-0.1943', '-0.7524', '-0.03256', '-0.2101', '0.653', '-0.5537', '-0.3833', '0.1989', '-0.1895', '0.01141', '0.2527', '-0.2477', '-0.1597', '-0.4631', '0.3835', '0.1128', '0.255', '-0.4695', '-0.044', '1.018', '0.1825', '-0.3396', '-0.1906', '0.649', '0.02086', '-0.04092', '-0.6284', '-0.605', '0.3525', '0.2144', '-0.05038', '-0.0142', '-0.1194', '0.0925', '0.10333', '0.964', '0.68', '0.4595', '-0.386', '0.3906', '-0.274', '0.4749', '-0.0807', '-0.2426', '0.5483', '-1.156', '0.6187', '-0.1984']",C84788,,,348.89,,10021750,
mondo:0018098,autosomal dominant limb-girdle muscular dystrophy type 1E (DES),"['limb-girdle muscular dystrophy type 1E', 'LGMD1E']",0110305,,34517,C3148763,,,,,,,,
mondo:0018100,familial primary hypomagnesemia,"['familial primary hypomagnesemia', 'primary familial hypomagnesemia', 'HOMG', 'hypomagnesemia']",0060879,,34526,,"['-0.08923', '-0.1434', '0.04346', '-0.3752', '0.253', '0.0635', '-0.4333', '0.578', '-0.1056', '0.353', '-0.528', '-0.433', '-0.06604', '0.548', '0.05396', '0.2837', '-0.5454', '-0.4453', '-0.00438', '-0.7695', '0.2756', '-0.8545', '0.2313', '0.2664', '0.1664', '0.4683', '-0.02693', '-0.1703', '0.1755', '-0.4038', '-0.556', '0.05112', '0.778', '0.2031', '-0.1575', '-0.09735', '-0.3909', '0.1575', '-0.569', '0.03333', '0.3193', '-0.1045', '0.2698', '-0.5386', '0.0962', '-1.019', '-0.1593', '0.3157', '-0.268', '0.8213', '-0.01412', '0.3352', '0.4783', '-0.789', '-0.2097', '-0.2119', '0.3662', '-0.05984', '-0.189', '-0.00861', '0.07324', '0.3516', '-0.1315', '-0.823', '-0.1648', '0.233', '0.4338', '0.645', '-0.306', '-0.2983', '0.187', '-0.137', '0.133', '0.2798', '0.1084', '0.7866', '0.3557', '0.0762', '-0.004322', '-0.3196', '0.49', '0.509', '0.2686', '0.4617', '0.2328', '0.5576', '0.3945', '-0.0897', '-0.01354', '-0.1467', '0.3235', '-0.5312', '0.4731', '-0.2742', '0.751', '0.271', '0.7207', '-0.589', '-0.4685', '0.3818']",C123263,,,,,,
mondo:0018101,familial primary hypomagnesemia with normocalciuria and normocalcemia,,,,34527,CN204443,"['-0.09894', '0.013565', '0.1901', '-0.706', '0.44', '-0.04358', '-0.0799', '1.211', '-0.9863', '-0.085', '-0.4692', '-0.1317', '-0.3079', '0.2622', '0.3853', '0.6377', '0.2118', '-0.3926', '0.2151', '-0.682', '0.425', '-0.1721', '0.2047', '0.4333', '0.553', '-0.4243', '-0.3682', '-0.00857', '-0.1412', '0.1692', '-0.1186', '0.1617', '0.4907', '-0.4636', '-0.1333', '-0.3489', '-0.6016', '0.2854', '-0.3054', '0.2438', '0.2369', '-0.8745', '0.3044', '-0.6626', '-0.07294', '-0.4395', '-0.8657', '0.1127', '-0.03114', '0.0705', '-0.3262', '0.4011', '-0.2214', '-0.4126', '-0.3992', '0.386', '0.4785', '-1.024', '-0.4312', '0.329', '-0.09717', '0.187', '0.2185', '-0.3044', '-0.5396', '-0.2347', '-0.1241', '0.5815', '-0.304', '-0.4502', '-0.04593', '0.0674', '0.4836', '0.0696', '0.62', '1.019', '0.526', '0.3845', '-0.2074', '-0.1038', '0.4712', '0.7056', '0.3066', '-0.09766', '0.2211', '0.735', '-0.16', '0.04922', '0.312', '0.1162', '0.1794', '0.294', '-0.1605', '-0.4016', '0.519', '0.9424', '0.517', '-0.9487', '-0.2607', '0.4705']",,,,,,,
mondo:0018102,corneal dystrophy,"['corneal dystrophy', 'corneal dystrophy (disease)']",2566,,34533,C0010036,,C34513,,D003317,371.50,,10011005,0001131
mondo:0018103,Quinquaud^s folliculitis decalvans,"['Quinquaud’s disease', 'Quinquaud^s decalvans folliculitis', 'folliculitis decalvans', 'Quinquaud^s disease']",,,346,CN227263,,,,,704.09,,,
mondo:0018105,Wolfram syndrome,"['diabetes insipidus-diabetes mellitus-optic atrophy-deafness syndrome', 'WFS', 'DIDMOAD', 'diabetes insipidus, diabetes mellitus, optic atrophy, and deafness syndrome', 'diabetes mellitus and insipidus with optic atrophy and deafness', 'DIDMOAD syndrome']",10632,,3463,CN184630,"['0.666', '0.0892', '-0.2152', '-0.2457', '-0.2169', '-0.2163', '0.1819', '0.677', '-0.6963', '0.3577', '-0.5283', '-1.137', '-0.5703', '0.4014', '-0.0948', '-0.346', '0.503', '0.4827', '0.0812', '-0.4573', '0.02011', '-0.3088', '0.0434', '-0.068', '-0.1197', '0.5137', '0.10284', '-0.6943', '0.5176', '-0.2693', '0.771', '0.1015', '0.2842', '-0.11743', '-0.1836', '-0.1688', '-0.1965', '0.01874', '-0.3635', '0.2634', '0.0427', '-0.4932', '0.9536', '0.099', '0.1459', '-0.8467', '0.4773', '0.1631', '-0.2485', '0.1653', '-0.0318', '0.7334', '-0.1531', '-1.261', '-0.1187', '0.3472', '0.5537', '-0.59', '-0.5728', '-0.228', '0.309', '0.0754', '0.2852', '0.3855', '-0.1343', '0.594', '0.11505', '-0.07623', '-0.744', '0.9917', '-0.0553', '-0.602', '0.1006', '-0.2373', '0.725', '-0.2725', '0.4404', '-0.489', '0.03165', '0.3198', '0.3616', '-0.653', '0.0204', '0.6523', '-0.371', '0.03714', '-0.188', '0.1414', '0.923', '-0.04825', '0.5693', '0.615', '0.06555', '-0.3123', '0.2998', '0.0771', '0.234', '-0.04654', '-0.3787', '0.739']",C35133,,D014929,250.80,,,
mondo:0018106,hereditary xanthinuria,"['hereditary xanthinuria', 'xanthine dehydrogenase deficiency', 'xanthic urolithiasis', 'xanthinuria', 'xanthine stone disease', 'classic xanthinuria']",0060236,,3467,,"['-0.2593', '0.04272', '-0.895', '0.1345', '-0.2788', '-0.1508', '-0.1869', '0.7544', '-0.1698', '0.4', '0.608', '-0.2198', '-0.4055', '0.3953', '-0.194', '0.1434', '0.2512', '0.1523', '-0.06836', '-0.4731', '-0.3987', '-0.274', '0.782', '-0.147', '0.1598', '0.05692', '0.1277', '0.2998', '0.3318', '0.07666', '0.4912', '-0.138', '-0.003407', '0.302', '-0.2263', '-0.508', '-0.3337', '-0.1821', '-0.0201', '-0.07025', '-0.542', '-0.31', '0.98', '-0.4104', '-0.434', '-0.4019', '0.03912', '-0.1279', '0.01791', '0.386', '0.3926', '-0.012054', '0.3472', '-0.335', '-0.3276', '-0.1621', '0.485', '-0.5415', '-0.6885', '-0.1068', '0.4324', '-0.1837', '0.05853', '-0.3523', '0.3125', '-0.1965', '0.7686', '0.5405', '-0.5527', '0.02744', '-0.2173', '0.0875', '-0.563', '0.07825', '0.4404', '0.5435', '0.2288', '-0.5317', '-0.0296', '0.2603', '-0.10974', '-0.278', '0.219', '0.7026', '0.538', '0.3306', '-0.2206', '-0.6836', '-0.02248', '-0.013214', '0.9585', '0.2063', '-0.4338', '-0.3665', '0.8735', '1.118', '0.4917', '-0.2622', '-0.436', '0.136']",,,,277.2,,,0010934
mondo:0018107,idiopathic recurrent and disabling cutaneous herpes,,,,35061,CN204468,,,,,,,,
mondo:0018108,idiopathic disseminated cytomegalovirus infection,['idiopathic disseminated CMV infection'],,,35062,CN204469,,,,,,,,
mondo:0018109,fulminant viral hepatitis,,,,35063,,,,,,,,10019772,
mondo:0018110,lethal idiopathic viral infection,,,,35064,CN776879,,,,,,,,
mondo:0018111,idiopathic severe pneumococcemia,,,,35065,,,,,,,,,
mondo:0018112,isolated scaphocephaly,"['isolated dolichocephaly', 'non-syndromic sagittal synostosis']",,,35093,,,,,,,,,
mondo:0018113,isolated plagiocephaly,"['non-syndromic unicoronal synostosis', 'synostotic plagiocephaly']",,,35098,,"['-0.256', '0.01051', '0.0935', '-0.08246', '-0.04047', '-0.03253', '0.29', '0.7134', '-0.4753', '-0.1357', '-0.0657', '-0.3196', '0.1315', '0.137', '-0.09235', '-0.1626', '0.5107', '-0.7686', '-0.479', '-0.6006', '-0.3018', '0.12067', '0.161', '-0.1827', '0.08514', '-0.1355', '-0.4622', '-0.2932', '0.4856', '0.5576', '0.1081', '-0.08386', '0.2042', '0.02629', '0.153', '0.1315', '0.1862', '-0.6562', '0.0002145', '-0.1401', '0.3079', '-0.01947', '0.503', '-0.896', '-0.249', '0.2401', '-0.041', '-0.3066', '-0.10364', '0.3657', '0.2612', '-0.3157', '-0.0618', '-0.2734', '-0.2233', '-0.301', '0.1436', '-0.145', '-0.0471', '0.1227', '0.1707', '-0.4614', '-0.2008', '0.102', '-0.1431', '0.0824', '0.1858', '0.2659', '-0.4417', '0.5254', '0.243', '0.7188', '0.2798', '-0.4507', '0.05017', '0.4546', '0.541', '-0.5117', '-0.776', '-0.4348', '-0.04416', '-0.0188', '0.2834', '0.814', '-0.039', '-0.2087', '-0.1328', '0.07336', '0.1677', '0.2112', '-0.342', '0.3564', '0.5293', '0.3586', '0.6646', '-0.1624', '0.5327', '-0.4727', '0.6035', '0.0438']",,,,,,,
mondo:0018114,isolated brachycephaly,['non-syndromic bicoronal synostosis'],,,35099,,"['-0.3042', '-0.03864', '-0.0579', '-0.0971', '0.1525', '0.2019', '0.1586', '0.9126', '-0.5625', '0.239', '-0.2233', '0.02751', '0.1266', '0.2969', '-0.4443', '-0.3127', '0.2883', '-0.278', '-0.2966', '-0.585', '-0.5317', '0.04532', '0.3286', '-0.3376', '0.7305', '0.4229', '-0.003925', '0.1873', '0.1554', '0.1555', '0.1572', '0.08057', '0.2393', '0.2834', '-0.2273', '-0.01425', '0.3926', '-0.442', '0.2378', '-0.619', '0.1184', '0.2094', '0.36', '-0.4915', '0.2192', '-0.002039', '0.3174', '0.01566', '-0.1625', '0.10913', '0.3416', '-0.5415', '0.1411', '-0.2764', '-0.321', '0.0245', '-0.011604', '-0.009674', '-0.02008', '0.3005', '-0.2213', '-0.0678', '-0.1396', '5.17e-05', '-0.1261', '-0.08344', '0.4307', '0.5874', '-0.516', '0.4539', '0.1', '0.716', '0.2969', '-0.696', '-0.4543', '-0.2812', '0.2512', '-0.3452', '-0.318', '-0.6353', '0.05124', '-0.135', '-0.367', '0.5723', '0.3162', '0.00634', '-0.10394', '-0.1155', '0.161', '-0.012794', '-0.506', '0.06525', '-0.2712', '0.3438', '0.3865', '0.06433', '0.971', '-0.2445', '0.591', '0.1268']",,,,,,,
mondo:0018115,epidermal nevus syndrome,['Epidermal hamartoma syndrome'],,,35125,,,,,,,,10014985,
mondo:0018116,galactosemia,"['galactosemia', 'galactosaemia', 'galactose intolerance']",9870,,352,C0016952,"['-0.999', '0.279', '0.2703', '0.4255', '0.552', '-0.2678', '-0.2817', '1.097', '-0.006187', '0.2324', '-0.11346', '-0.5596', '-0.6045', '0.5825', '0.004093', '0.0315', '0.1599', '-0.1626', '-0.36', '-0.924', '0.02805', '0.2495', '0.8926', '0.1367', '-0.589', '0.173', '-0.6055', '-0.1587', '0.3', '-0.1343', '0.7188', '0.03677', '0.1844', '0.8433', '-0.4573', '0.4956', '-0.757', '0.11084', '-0.594', '-0.05353', '-0.2947', '-0.2302', '-0.03363', '-0.1826', '-0.2347', '-0.1578', '0.4827', '-0.02583', '0.398', '0.5303', '0.1996', '0.05508', '0.2136', '-1.297', '-0.3188', '-0.2277', '0.2686', '-0.1377', '-0.3289', '-0.08093', '-0.2517', '-0.004524', '0.509', '-0.05685', '0.2008', '0.273', '-0.1914', '-0.09076', '-0.6084', '0.2256', '-0.6743', '0.1655', '0.139', '0.0907', '0.0678', '0.1808', '0.3206', '-0.1758', '-0.2644', '-0.3655', '-0.7207', '-0.711', '-0.5435', '0.2324', '0.687', '0.4534', '0.4756', '0.02882', '0.5747', '0.1332', '0.526', '0.1501', '0.02174', '-0.046', '0.5415', '0.342', '0.2673', '-0.03622', '0.407', '0.4092']",C84723,,D005693,271.1,,10017604,
mondo:0018117,"disorder of phospholipids, sphingolipids and fatty acids biosynthesis",,,,352301,CN227264,,,,,,,,
mondo:0018121,mitochondrial DNA maintenance syndrome,"['inborn error of mitochondrial genome maintenance', 'rare inborn error of mitochondrial genome maintenance', 'mtDNA maintenance syndrome']",,,352456,CN204491,,,,,,,,
mondo:0018122,digital anomalies-intellectual disability-short stature syndrome,,,,352487,CN204494,,,,,,,,
mondo:0018123,intellectual disability-obesity-brain malformations-facial dysmorphism syndrome,['autosomal recessive intellectual disability due to TRAPPC9 deficiency'],,,352530,CN204496,,,,,,,,
mondo:0018124,Oncogenic osteomalacia,"['OO', 'tumor-induced osteomalacia', 'Oncogenic hypophosphatemic osteomalacia', 'OOM', 'TIO']",,,352540,C1274103,,C67235,,C537751,,,,
mondo:0018125,focal epilepsy-intellectual disability-cerebro-cerebellar malformation,['focal epilepsy-intellectual disability-dysarthria-ataxia syndrome'],,,352587,CN204502,,,,,,,,
mondo:0018126,progressive myoclonic epilepsy with dystonia,"['PMED', 'progressive myoclonus epilepsy with dystonia']",,,352596,,,,,,,,,
mondo:0018127,16q24.1 microdeletion syndrome,"['Del(16)(q24.1)', 'monosomy 16q24.1']",,,352629,CN204505,,,,,,,,
mondo:0018128,phalangeal microgeodic syndrome,['phalangeal osteolysis'],,,352636,CN204506,,,,,,,,
mondo:0018129,autosomal recessive cerebellar ataxia with late-onset spasticity,['autosomal recessive cerebellar ataxia due to GBA2 deficiency'],,,352641,CN204507,,,,,,,,
mondo:0018130,brain dopamine-serotonin vesicular transport disease,,,,352649,CN204508,,,,,,,,
mondo:0018131,neurodevelopmental disorder-craniofacial dysmorphism-cardiac defect-hip dysplasia syndrome due to 9q21 microdeletion,"['9q21 microdeletion syndrome', 'Del(9)(q21)']",,,352665,CN204512,,,,,,,,
mondo:0018133,attenuated Chédiak-Higashi syndrome,"['atypical Chédiak-Higashi syndrome', 'attenuated Chediak-Higashi syndrome', 'atypical Chediak-Higashi syndrome']",,,352723,CN204519,,,,,,E70.3,,
mondo:0018134,disorder of melanin metabolism,,,,352728,CN227269,,,,,,,,
mondo:0018135,oculocutaneous albinism type 1,"['oculocutaneous albinism, tyrosinase negative', 'OCA1', 'ATN']",,,352731,CN119529,"['0.4243', '0.10266', '-0.29', '0.0524', '0.3884', '-0.1444', '-0.316', '0.2087', '-0.4443', '-0.4656', '0.4934', '-0.1742', '0.0815', '0.9355', '-0.1326', '0.4604', '0.581', '-0.0466', '0.412', '-0.4717', '-0.8057', '0.06183', '0.6074', '-0.359', '-0.1644', '0.068', '-0.6963', '-0.1681', '0.4468', '0.2032', '0.4475', '0.1328', '0.1223', '0.5303', '-0.03107', '0.2495', '-0.897', '-0.4404', '-0.1613', '-0.479', '1.367', '-0.3684', '-0.1406', '-0.263', '-0.5054', '-0.7407', '0.609', '-1.01', '1.056', '0.512', '0.12115', '-0.607', '0.3662', '-0.344', '0.659', '0.4094', '0.4185', '0.745', '0.03195', '-0.829', '-0.4119', '0.2123', '0.6855', '0.4697', '-0.1926', '0.1566', '0.1919', '0.256', '-0.3533', '0.5825', '-0.2715', '0.3816', '-0.2069', '0.02971', '0.811', '0.0451', '0.2289', '-0.1644', '0.02844', '-0.07666', '0.565', '-0.4438', '0.4114', '0.5596', '-0.3394', '-1.459', '0.547', '0.721', '0.9624', '0.475', '0.1938', '1.007', '0.0922', '-0.2698', '0.8164', '0.4187', '-0.4583', '-0.3389', '0.3047', '0.5215']",,,C537728,,,,
mondo:0018136,minimal pigment oculocutaneous albinism type 1,"['OCA1-MP', 'MP OCA type 1']",,,352734,CN204521,,,,,270.2,,,
mondo:0018137,temperature-sensitive oculocutaneous albinism type 1,"['TS OCA type 1', 'OCA1-TS']",,,352737,C1847132,,,,,,,,
mondo:0018141,"pyruvate carboxylase deficiency, infantile form","['pyruvate carboxylase deficiency type A', 'pyruvate carboxylase deficiency, infantile type']",,,353308,CN204538,,,,,,,,
mondo:0018142,"pyruvate carboxylase deficiency, severe neonatal type",['pyruvate carboxylase deficiency type B'],,,353314,CN204539,,,,,,,,
mondo:0018143,"pyruvate carboxylase deficiency, benign type",['pyruvate carboxylase deficiency type C'],,,353320,CN204540,,,,,,,,
mondo:0018144,congenital myasthenic syndromes with glycosylation defect,,,,353327,,"['-0.1265', '0.07544', '0.05212', '-0.00724', '0.0695', '-0.1375', '-0.02158', '0.1002', '-0.052', '-0.10583', '-0.01637', '-0.09314', '0.04492', '0.04996', '-0.0874', '-0.0317', '-0.00751', '-0.0759', '-0.00815', '-0.3066', '0.01813', '0.03598', '0.1508', '-0.05157', '0.02046', '-0.00508', '-0.0642', '-0.0934', '0.0709', '-0.1181', '0.1105', '0.1225', '0.1544', '0.1233', '-0.02289', '-0.03336', '0.02888', '-0.0183', '-0.1377', '-0.1156', '0.06793', '-0.1442', '-0.02707', '-0.02248', '-0.004456', '-0.1514', '0.005547', '0.1184', '0.1086', '0.071', '-0.1044', '-0.01268', '0.00761', '0.02412', '-0.1525', '-0.0888', '0.1135', '0.01889', '-0.11945', '0.06714', '0.1172', '0.0224', '0.07666', '0.06726', '-0.0175', '-0.0224', '0.11786', '0.07294', '-0.1909', '0.1383', '-0.11', '0.09644', '0.05203', '-0.01677', '0.09937', '0.0376', '0.0663', '-0.0344', '-0.1584', '-0.03235', '-0.03394', '0.00508', '-0.039', '0.0802', '-0.01483', '-0.0657', '0.0668', '0.13', '0.08795', '0.01929', '0.0997', '0.11285', '0.05188', '0.03677', '0.1714', '0.1019', '0.1499', '-0.2058', '0.00429', '0.09656']",,,,,,,
mondo:0018145,congenital retinal arteriovenous communication,"['congenital arteriovenous communication of the retina', 'congenital retinal arteriovenous anastomoses', 'congenital arteriovenous anastomoses of the retina']",,,353334,,,,,,,,,
mondo:0018146,idiopathic macular telangiectasia type 1,"['aneurysmal telangiectasia', 'visible and exudative idiopathic juxtafoveolar retinal telangiectasis']",,,353344,CN204544,,,,,,H35.5,,
mondo:0018147,idiopathic macular telangiectasia type 3,['occlusive idiopathic juxtafoveolar retinal telangiectasis'],,,353351,CN204545,,,,,,H35.5,,
mondo:0018148,vasoproliferative tumor of retina,"['retinal vasoproliferative tumor', 'vasoproliferative tumor of the ocular fundus', 'VPTR', 'vasoproliferative tumour of the retina', 'vasoproliferative tumor of the retina', 'vasoproliferative tumour of ocular fundus', 'retinal vasoproliferative tumour', 'vasoproliferative tumor of ocular fundus', 'vasoproliferative tumour of the ocular fundus']",,,353356,CN204546,,,,,,,,
mondo:0018149,GM1 gangliosidosis,"['GM>1< gangliosidosis', 'Landing syndrome', 'gangliosidosis GM1', 'Beta-galactosidase deficiency', 'beta-galactosidase deficiency', 'Beta galactosidase 1 deficiency', 'GLB 1 deficiency', 'Beta-galactosidase-1 deficiency', 'Beta-galactosidosis', 'GLB1 deficiency', 'deficiency of beta-galactosidase', 'Landing disease']",3322,,354,C0085131,"['-0.10565', '0.6226', '-0.2847', '0.2224', '0.12476', '-0.872', '0.0985', '0.873', '-0.8164', '0.525', '-0.2502', '0.5312', '0.10156', '0.12146', '0.571', '0.1306', '0.4626', '-0.458', '-0.4949', '-0.281', '0.04236', '-0.303', '0.624', '0.02602', '0.0614', '-0.3096', '-0.06128', '0.268', '-0.7627', '-0.09094', '0.5283', '0.2905', '0.358', '-0.09467', '-0.1803', '-0.2712', '-0.5625', '-0.137', '-0.266', '0.1096', '0.0346', '-0.492', '-0.0192', '0.04816', '0.5615', '-0.03238', '0.1389', '0.176', '-0.12396', '-0.0818', '-0.08124', '-0.3252', '-0.0213', '-0.4878', '0.1648', '-0.3872', '0.412', '-0.1659', '-0.456', '-0.1367', '-0.303', '-0.1382', '0.7886', '0.1874', '-0.0397', '-0.11395', '0.6343', '-0.2274', '-0.2683', '0.1138', '0.01494', '0.01854', '0.0841', '0.04077', '0.6333', '0.6377', '0.1378', '-0.0334', '-0.5493', '-0.1001', '0.1887', '-0.5386', '-0.2256', '0.2698', '0.125', '0.02818', '0.0701', '-0.0008655', '0.3635', '-0.0583', '0.294', '0.563', '0.04614', '-0.1112', '-0.04153', '0.472', '-0.0408', '0.01256', '0.2903', '0.1071']",C84739,,D016537,277.6,,,
mondo:0018150,Gaucher disease,"['glocucerebrosidase deficiency', 'glucosyl cerebroside lipidosis', 'lipoid histiocytosis (kerasin type)', 'glucosylceramide beta-glucosidase deficiency', 'acute cerebral Gaucher disease', 'Gaucher disease', 'sphingolipidosis 1', 'glucocerebrosidase deficiency', 'kerasin thesaurismosis', 'Gaucher^s disease', 'acid beta-glucosidase deficiency']",1926,,355,C0017205,"['-0.1924', '0.716', '0.10913', '-0.8286', '-0.2615', '-0.4587', '0.1534', '1.121', '-1.334', '-0.505', '-0.3323', '-0.0977', '-0.2042', '0.8486', '0.2517', '-0.9517', '-0.0887', '0.2421', '-0.643', '-0.5713', '-0.578', '-0.5894', '0.4158', '-0.4968', '-0.2095', '-0.1459', '0.2627', '0.8564', '0.5425', '-0.2323', '0.627', '0.2452', '0.5347', '0.2', '0.11334', '0.239', '-0.4185', '-0.2206', '-0.03986', '-0.1418', '0.387', '-0.4626', '-0.0553', '-0.389', '-0.2834', '-0.01488', '-0.10486', '-0.2145', '-0.277', '-0.2048', '0.6025', '0.4377', '0.9556', '-0.566', '0.4692', '-0.5273', '-0.03275', '0.1774', '0.2245', '-0.4922', '0.06055', '-0.06934', '0.7007', '-0.7656', '-0.2283', '0.2417', '-0.0609', '-0.2947', '-0.6055', '-0.376', '0.1858', '0.0855', '-0.1766', '-0.002155', '0.5015', '0.304', '0.03084', '0.298', '-0.3171', '-0.7246', '-0.4077', '-0.8735', '-0.0826', '-0.3284', '-0.7183', '-0.4478', '1.108', '0.1707', '0.314', '0.02226', '-0.1991', '-0.4116', '0.04434', '0.135', '0.6816', '1.18', '-0.1986', '0.01356', '0.557', '-1.121']",C61268,,D005776,,E75.22,10018048,
mondo:0018151,coenzyme Q10 deficiency,"['CoQ10 deficiency, primary', 'coenzyme Q10 deficiency, primary', 'coenzyme Q10 deficiency disease', 'CoQ10 deficiency']",0050730,,35656,CN229570,"['-0.2314', '0.2003', '-0.04575', '0.0484', '0.145', '-0.1245', '-0.00848', '-0.003271', '-0.1003', '-0.1886', '-0.0478', '0.05554', '0.0574', '-0.0897', '0.0951', '-0.007706', '-0.15', '0.00925', '-0.09674', '-0.464', '-0.0505', '-0.1696', '0.169', '0.1149', '-0.0013485', '-0.122', '0.04724', '-0.1604', '0.02815', '-0.1771', '0.2266', '0.1664', '0.09924', '0.1516', '-0.04913', '-0.1406', '0.0986', '-0.1476', '-0.02998', '-0.2917', '0.02454', '-0.3083', '0.1571', '0.0222', '-0.01637', '-0.346', '0.009895', '0.0965', '0.1812', '0.1274', '0.1515', '-0.1227', '-0.0723', '-0.0713', '-0.04865', '-0.3599', '0.2242', '0.03802', '-0.304', '0.1396', '0.1203', '0.0692', '0.1425', '-0.0774', '0.05954', '0.0376', '0.1989', '0.087', '-0.261', '0.11865', '-0.2036', '-0.249', '-0.0765', '-0.01499', '0.2051', '0.2227', '0.09875', '0.05832', '-0.1742', '0.02954', '0.1566', '-0.0348', '0.00377', '0.2217', '0.05328', '0.002445', '0.08563', '0.0632', '0.1951', '0.05585', '0.2416', '0.1583', '-0.11597', '-0.06464', '0.4536', '0.271', '0.2283', '-0.2422', '-0.10876', '0.0449']",C142083,,C564403,,,,
mondo:0018152,serpiginous choroiditis,"['serpiginous choroidopathy', 'peripapillary choriopathy', 'geographic helicoid peripapillary choroidopathy', 'geographic serpiginous choroiditis', 'geographic choroiditis', 'geographic helicoid peripapillary choroidopathy (GHPC)']",,,35686,C0729842,,,,,363.8,,,
mondo:0018153,Erdheim-Chester disease,"['ECD', 'Erdheim-Chester disease', 'lipogranulomatosis', 'polyostotic sclerosing histiocytosis', 'lipoid granulomatosis', 'Erdheim Chester disease']",4329,,35687,C0878675,,C53972,1000926,D031249,277.89,,10060801,
mondo:0018154,Madelung deformity,,,,35688,,"['-0.6694', '0.11176', '0.3628', '-0.1891', '0.3147', '-0.234', '0.2114', '0.609', '-0.616', '-0.1439', '-0.0435', '0.04895', '0.1747', '0.1979', '-0.1326', '-0.2094', '0.2515', '-0.11884', '-0.01688', '-0.6616', '0.07886', '0.0103', '0.256', '-0.1423', '0.3997', '0.2396', '-0.003384', '0.0923', '-0.1818', '0.03616', '-0.02872', '-0.0525', '-0.1222', '0.2698', '0.1754', '-0.2886', '0.3398', '-0.0988', '-0.2217', '-0.0918', '-0.2109', '-0.3362', '0.0626', '0.10266', '0.1477', '-0.1259', '0.05273', '0.2522', '0.142', '0.05493', '-0.03647', '-0.3523', '0.0953', '0.1407', '-0.5337', '-0.4514', '0.1163', '-0.05798', '-0.355', '-0.0559', '0.1376', '-0.006683', '-0.422', '-0.03766', '-0.093', '0.0561', '0.09393', '0.149', '-0.1071', '0.07983', '0.05563', '0.2683', '0.4163', '-0.2456', '-0.1062', '0.09564', '-0.06177', '-0.00973', '-0.4907', '-0.326', '-0.1436', '-0.03635', '0.2076', '0.421', '-0.2147', '0.0005107', '-0.1771', '0.02007', '0.2102', '-0.2703', '-0.1937', '0.0685', '0.04407', '0.2815', '0.3542', '0.0537', '0.432', '-0.507', '0.1364', '0.1495']",,,C562398,755.54,,10007700,
mondo:0018155,lateral sclerosis,"['PLS', 'adult-onset PLS', 'adult-onset primary lateral sclerosis', 'primary lateral sclerosis']",230,,35689,C0154682,,C129933,,,335.24,,10036704,
mondo:0018156,3q26q27 microdeletion syndrome,"['monosomy 3q26q27', 'Del(3)(q26q27)', 'monosomy 3q26-q27', '3q26-q27microdeletion syndrome']",,,356947,CN204590,,,,,,,,
mondo:0018158,mitochondrial DNA depletion syndrome,['mtDNA depletion syndrome'],0070329,,35698,CN239350,"['-0.4683', '0.15', '0.2695', '-0.2004', '-0.0535', '-0.4795', '-0.1849', '0.1089', '-0.5757', '0.10864', '-0.3384', '-0.4817', '0.1326', '-0.0687', '-0.01547', '-0.1659', '-0.435', '-0.2515', '-0.1818', '-0.5947', '0.1616', '-0.1534', '0.3142', '-0.2095', '0.2373', '0.104', '-0.1692', '-0.1346', '0.013016', '-0.2605', '0.10345', '0.258', '0.502', '0.05664', '0.04156', '-0.3015', '-0.611', '0.1521', '-0.6396', '-0.2615', '0.04828', '-0.598', '-0.1968', '0.2532', '0.1353', '-0.3733', '-0.4128', '0.06964', '0.11255', '0.1626', '-0.403', '0.1721', '0.01804', '-0.0005374', '0.1235', '-0.3826', '0.3176', '-0.04617', '-0.1606', '0.4927', '0.1904', '0.02069', '0.3035', '0.3115', '-0.6216', '-0.1514', '-0.03262', '0.01897', '-0.265', '0.4097', '-0.1725', '-0.03745', '0.1266', '0.2969', '0.2264', '0.1365', '0.08026', '-0.02502', '-0.2856', '-0.03818', '0.294', '-0.0327', '-0.1276', '0.0586', '0.04175', '0.3042', '0.2725', '0.346', '0.3347', '-0.3398', '0.505', '0.1057', '0.0754', '-0.378', '0.2827', '0.3445', '0.364', '0.05603', '-0.169', '0.4485']",,,,,,10059396,
mondo:0018159,atypical hemolytic-uremic syndrome with DGKE deficiency,"['D-HUS with DGKE deficiency', 'hemolytic-uremic syndrome without diarrhea with DGKE deficiency', 'hemolytic-uremic syndrome without diarrhoea with DGKE deficiency', 'atypical HUS with DGKE deficiency', 'aHUS with DGKE deficiency']",0080388,,357008,CN204596,"['-0.07965', '0.1427', '-0.01996', '0.003735', '0.03604', '-0.1632', '0.001415', '0.1021', '-0.046', '-0.05753', '-0.02553', '-0.0421', '0.02385', '-0.02487', '-0.0409', '-0.0886', '-0.03522', '-0.02768', '-0.09875', '-0.272', '-0.01167', '-0.086', '0.1229', '-0.0998', '0.0618', '-0.012985', '-0.1003', '-0.07306', '0.03763', '-0.08167', '0.1306', '0.0486', '0.219', '0.11774', '0.03723', '-0.1307', '0.002975', '-0.1225', '-0.02507', '-0.1938', '0.0499', '-0.1736', '0.0302', '-0.0753', '-0.01122', '-0.1627', '-0.03638', '0.1066', '0.002043', '0.05655', '-0.03403', '-0.03104', '-0.01776', '0.04095', '-0.1317', '-0.02274', '0.1613', '-0.05103', '-0.1976', '0.0831', '0.117', '0.07086', '0.04837', '0.0151', '0.0339', '0.00938', '0.205', '0.0608', '-0.1431', '0.1611', '-0.1487', '-0.007336', '0.01892', '-0.1323', '0.05032', '0.03244', '0.01243', '0.00808', '-0.0777', '-0.0228', '0.0314', '0.04846', '-0.05136', '0.1205', '-0.01636', '-0.0664', '0.0749', '0.1677', '0.194', '0.00955', '0.1765', '0.12164', '0.001876', '0.009735', '0.2817', '0.13', '0.1532', '-0.246', '0.007587', '0.0687']",,,,,,,
mondo:0018160,hereditary retinoblastoma,"['retinoblastoma, autosomal dominant, somatic mutation', 'retinoblastoma, trilateral, autosomal dominant, somatic mutation', 'hereditary retinoblastoma', 'RB1', 'familial retinoblastoma']",4648,180200,357027,,,C8495,,,,,,
mondo:0018161,non-hereditary retinoblastoma,,,,357034,CN204600,,,,,,,,
mondo:0018162,neurometabolic disorder due to serine deficiency,['serine deficiency'],,,35705,CN227274,,,,,,,,
mondo:0018163,autosomal recessive cutis laxa type 2A,"['cutis laxa with growth and developmental delay', 'ARCL2A', 'cutis laxa, autosomal recessive, type 2A', 'cutis laxa, autosomal recessive, type IIA', 'cutis laxa with congenital disorder of glycosylation', 'autosomal recessive cutis laxa type IIA', 'cutis laxa with bone dystrophy', 'cutis laxa, debre type', 'cutis laxa with Joint laxity and retarded development', 'cutis laxa, autosomal recessive type 2A']",0070134,219200,357058,,"['-0.1613', '0.1333', '0.286', '-0.4104', '0.726', '-0.377', '-0.4966', '0.2656', '-0.7007', '0.01672', '-0.2188', '-0.06232', '0.2465', '-0.1626', '-0.05154', '0.382', '0.2913', '-0.4114', '-0.04767', '-0.453', '0.03973', '-0.02075', '0.0392', '0.0693', '0.1865', '0.00668', '-0.1604', '0.02748', '0.4297', '-0.2651', '0.543', '0.0596', '0.421', '0.0708', '0.06433', '-0.2329', '-0.393', '-0.1148', '-0.0873', '-0.4924', '0.2554', '-0.5166', '-0.03787', '0.2427', '-0.007008', '-0.09247', '0.0634', '0.3525', '-0.1107', '-0.1702', '-0.03934', '-0.1396', '0.06158', '0.371', '-0.3232', '-0.3376', '-0.06665', '0.287', '-0.10504', '0.1748', '-0.0213', '0.0585', '-0.4136', '0.0858', '0.2498', '0.014595', '0.283', '0.4094', '-0.3943', '0.3687', '-0.4612', '0.0886', '0.1769', '-0.1997', '-0.04465', '-0.0369', '0.1571', '-0.2769', '-0.0005064', '-0.12103', '0.1528', '0.007416', '-0.185', '0.253', '-0.1917', '0.3503', '-0.2505', '0.5137', '0.06805', '0.2896', '-0.05347', '0.5767', '0.3594', '0.04626', '0.681', '0.08386', '0.3186', '-0.1317', '0.5806', '0.0686']",,,,,,,
mondo:0018164,arterial thoracic outlet syndrome,"['arterial cervical rib syndrome', 'arterial hyperabduction syndrome', 'arterial costoclavicular syndrome', 'arterial scalenus anticus syndrome', 'ATOS', 'arterial thoracic outlet compression syndrome', 'arterial TOS']",,,357107,C1956395,,,,,,,,
mondo:0018165,venous thoracic outlet syndrome,"['Venous scalenus anticus syndrome', 'Venous TOS', 'Venous thoracic outlet compression syndrome', 'Paget-Schrotter disease', 'effort subclavian vein thrombosis', 'Venous cervical rib syndrome', 'VTOS', 'Venous hyperabduction syndrome', 'Venous costoclavicular syndrome']",,,357131,C1956396,,,,,,,,
mondo:0018166,oral submucous fibrosis,"['oral cavity submucous fibrosis', 'OSMF', 'oral submucosal fibrosis', 'oral submucosal fibrosis, including of tongue']",5773,,357154,C0029172,,C34866,1001818,D009914,528.8,K13.5,,
mondo:0018167,primary essential cutis verticis gyrata,,,,357220,CN204615,,,,,,,,
mondo:0018168,primary non-essential cutis verticis gyrata,,,,357225,CN204616,,,,,,,,
mondo:0018169,morning glory syndrome,"['Volubilis syndrome', 'Ectasic coloboma']",,,35737,C0549307,"['0.0444', '-0.1471', '-0.446', '0.343', '-0.04224', '0.11755', '0.1097', '0.5576', '-0.356', '-0.3845', '0.2078', '-0.722', '-0.357', '0.08575', '-0.3525', '-0.1669', '0.00764', '-0.2554', '0.3547', '-0.4688', '-0.202', '-0.2291', '0.2072', '-0.2874', '0.03723', '0.2439', '-0.6333', '0.1841', '0.4873', '0.4143', '0.3032', '-0.6147', '0.6567', '0.3228', '0.01294', '0.077', '0.1661', '-0.6006', '-0.4097', '-0.5654', '0.2', '0.6533', '0.265', '-0.414', '0.2335', '0.4775', '0.1594', '0.3704', '-0.4895', '-0.0849', '0.8853', '0.3215', '-0.02908', '-0.657', '0.06012', '0.3015', '0.1572', '-0.6577', '-0.7773', '-0.01333', '-0.03836', '0.2313', '0.332', '0.1346', '-0.3884', '-0.0624', '0.392', '0.586', '0.03552', '0.2808', '-0.2766', '0.3228', '-0.243', '-0.3542', '0.04504', '-0.419', '0.4175', '-0.0779', '-0.7217', '-0.6743', '-0.0639', '0.1604', '0.3318', '1.15', '-0.38', '-0.2925', '0.339', '0.3796', '0.392', '0.2491', '0.3867', '0.1137', '0.2712', '-0.07526', '0.7593', '-0.4292', '0.3962', '-0.4924', '-0.3274', '0.5444']",,,,,,10027974,
mondo:0018170,idiopathic nephrotic syndrome,,,,357502,C3496337,,C122796,,,,,,
mondo:0018171,malignant germ cell tumor of ovary,"['malignant germ cell neoplasm of the ovary', 'malignant ovarian germ cell neoplasm', 'malignant germ cell neoplasm of ovary', 'malignant ovarian germ cell tumour', 'MOGCT', 'ovary malignant germ cell tumor', 'ovarian germ cell cancer', 'ovary malignant germ cell tumour', 'malignant germ cell tumor of ovary', 'malignant germ cell tumor of the ovary', 'malignant ovarian germ cell tumor', 'malignant germ cell tumour of the ovary']",2155,,35807,C0346180,,C4514,,,,,,
mondo:0018172,malignant sex cord stromal tumor of ovary,"['malignant Sex cord-stromal tumour of ovary', 'malignant ovarian SCST', 'malignant ovarian Sex cord-stromal tumor', 'ovarian sex cord-stromal tumor, malignant', 'malignant Sex cord-stromal tumour of the ovary', 'malignant ovarian Sex cord-stromal neoplasm', 'malignant Sex cord-stromal tumor of ovary', 'malignant ovarian Sex cord-stromal tumour', 'malignant ovarian sex cord-stromal tumour', 'malignant ovarian sex cord-stromal tumor', 'malignant Sex cord-stromal tumor of the ovary']",,,35808,CN204631,,C8053,,,,,,
mondo:0018173,acute opioid poisoning,,,,35889,CN227277,,,,,,,,
mondo:0018174,hereditary glaucoma,"['hereditary glaucoma (disease)', 'glaucoma, hereditary']",,,359,CN227278,,,,C580055,,,,
mondo:0018175,combined deficiency of factor V and factor VIII,"['combined deficiency of factor V and factor type VIII', 'FV and FVIII combined deficiency', 'F5F8D', 'familial multiple coagulation factor deficiency']",,,35909,C1856883,"['-0.2556', '0.002058', '-0.522', '-0.6235', '0.01964', '0.2898', '-0.02611', '0.6377', '-0.465', '0.00144', '-0.397', '0.521', '0.2876', '0.03534', '0.2397', '-0.2388', '0.4106', '0.1891', '-0.585', '-0.7124', '-0.6587', '-0.7046', '1.011', '0.425', '0.000297', '0.05426', '0.3267', '0.09033', '0.2107', '0.049', '0.399', '-0.202', '0.315', '0.1566', '-0.01663', '-0.2996', '-0.299', '-0.3718', '0.2084', '-0.4116', '-0.3374', '-0.541', '0.61', '0.2124', '0.303', '0.08496', '-0.4163', '0.05746', '0.49', '0.3315', '0.515', '-0.51', '0.1622', '-0.2207', '-0.205', '0.2834', '0.4414', '0.2382', '-0.6016', '-0.07214', '-0.3242', '0.257', '0.5684', '-0.0505', '0.3186', '0.5396', '0.0613', '-0.3547', '-0.332', '-0.3384', '-0.5474', '-0.2449', '-0.2734', '-0.2761', '1.195', '0.2842', '1.094', '0.1489', '0.4807', '-0.05402', '-0.3357', '-0.481', '-0.2559', '-0.005802', '0.06247', '0.0706', '-0.02203', '0.917', '0.2927', '-0.478', '-0.3162', '0.5054', '0.252', '-0.4038', '0.83', '0.884', '0.06976', '-0.808', '-0.1947', '-0.0731']",,,,,,,
mondo:0018177,glioblastoma,"['giant cell glioblastoma (histologic variant)', 'glioblastoma multiforme (disease)', 'glioblastoma (disease)', 'spongioblastoma multiforme', 'grade IV astrocytic neoplasm', 'GBM (glioblastoma)', 'gliosarcoma (histologic variant)', 'primary glioblastoma multiforme', 'grade IV adult astrocytic tumor', 'WHO grade IV glioma', 'glioblastoma', 'grade IV astrocytic tumor', 'grade IV astrocytic tumour', 'grade IV astrocytoma', 'GBM', 'glioblastoma multiforme', 'grade IV adult astrocytic tumour']",3068,,360,CN227279,,C3058,0000519,D005909,,,10018337,0100843
mondo:0018178,intestinal lymphangiectasia,"['intestinal lymphangiectasia', 'intestinal lymphangiectasia (disease)']",,,36204,,,,,,457.1,,10025213,0002593
mondo:0018180,staphylococcal scarlet fever,,,,36235,CN204670,,,,,,A38,,
mondo:0018181,staphylococcal scalded skin syndrome,"['Ritter^s disease', 'Ritter disease', 'SSSS', 'scalded skin syndrome', 'staphylococcal scalded skin syndrome', 'generalised exfoliative disease', 'toxic epidermal necrolysis, subcorneal type', 'generalized exfoliative disease', 'pemphigus neonatorum', 'dermatitis exfoliativa neonatorum']",9063,,36236,C0678185,,C85077,0007473,D013206,695.81,L00,10041929,
mondo:0018182,bullous impetigo,,,,36237,C0021100,,,,,,L01.03,10006563,
mondo:0018183,staphylococcal necrotizing pneumonia,,,,36238,,,,,,,,,
mondo:0018184,gastric linitis plastica,"['Borrmann gastric cancer type 4', 'linitis plastica of the stomach']",,,36273,CN204677,,,,,,,,
mondo:0018185,congenital anomaly of the great veins,,,,363189,,,,,,,,,
mondo:0018187,hereditary syndromic Pierre Robin syndrome,['genetic syndromic Pierre Robin syndrome'],,,363294,CN204685,,,,,,,,
mondo:0018188,hereditary intestinal polyposis,"['genetic intestinal polyposis', 'familial intestinal polyposis']",,,363314,C2713443,,,,,,,,
mondo:0018189,autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome,,,,363429,CN204693,"['-0.1226', '-0.2288', '0.097', '-0.0694', '-0.2715', '-0.973', '0.0999', '0.0345', '-0.786', '-0.794', '0.0812', '0.1727', '-0.2231', '0.2288', '0.455', '-0.2847', '-0.10486', '-0.2974', '0.2354', '-0.747', '-0.178', '-0.237', '0.2496', '-0.4883', '0.563', '-0.3994', '-0.2915', '0.2744', '-0.1753', '-0.8115', '-0.04214', '0.4204', '-0.409', '-0.112', '0.3936', '0.04654', '-0.2964', '-0.00511', '0.4614', '0.335', '0.4077', '0.3242', '-0.483', '0.3835', '0.503', '-0.405', '0.2551', '0.549', '0.272', '-0.09406', '-0.2615', '0.2351', '-0.1032', '-0.5586', '0.01218', '-0.586', '0.3367', '0.5664', '-0.1304', '0.582', '-0.4614', '0.3916', '0.26', '-0.04092', '-0.4087', '0.536', '0.3462', '0.4883', '-0.4326', '0.5234', '0.872', '0.582', '-0.0903', '-0.5386', '0.6353', '0.2654', '0.3572', '0.319', '0.2119', '0.3706', '-0.2491', '-0.742', '0.3018', '0.983', '-0.3257', '-0.5303', '0.05203', '0.0428', '0.4634', '0.7007', '0.514', '0.5933', '-0.04474', '0.1039', '0.9893', '1.02', '0.4668', '0.398', '-0.2656', '0.02708']",,,,,,,
mondo:0018190,autosomal dominant childhood-onset proximal spinal muscular atrophy,"['lower extremity-predominant autosomal dominant proximal spinal muscular atrophy', 'spinal muscular atrophy, lower extremity-predominant', 'SMALED']",0070348,,363447,CN227282,"['-0.2303', '0.0909', '-2.164e-05', '-0.2659', '0.2059', '-0.552', '-0.01863', '0.4465', '-0.563', '0.002268', '-0.1799', '0.04785', '-0.2922', '0.1111', '0.3252', '-0.0459', '-0.005833', '-0.196', '-0.1447', '-0.486', '-0.04388', '-0.10626', '0.369', '-0.00606', '-0.0922', '-0.00574', '-0.0347', '-0.1528', '-0.1646', '-0.2399', '0.2028', '0.2101', '0.328', '0.1365', '-0.11285', '-0.2383', '-0.1532', '0.01715', '0.04343', '-0.153', '-0.112', '-0.3728', '-0.1117', '0.1738', '-0.2136', '-0.0792', '-0.1461', '0.1562', '0.02855', '0.04858', '0.04733', '-0.02106', '0.03452', '-0.199', '-0.0487', '-0.365', '0.2517', '-0.08014', '-0.01253', '-0.03226', '0.0949', '-0.06525', '0.1239', '0.102', '-0.3186', '0.0635', '0.3215', '0.6196', '-0.255', '-0.1503', '-0.4775', '-0.12225', '0.2046', '0.08496', '0.3557', '0.01962', '0.1025', '-0.0938', '-0.0705', '-0.247', '0.09', '0.01718', '0.09906', '0.5303', '-0.01351', '0.3884', '0.03726', '0.0845', '0.203', '-0.0631', '0.2358', '0.2502', '0.2065', '0.1287', '0.4683', '0.0787', '0.6523', '-0.0336', '0.05878', '0.07855']",,,,,,,
mondo:0018191,tumor of testis and paratestis,"['testicular and paratesticular tumor', 'testicular and paratesticular tumour']",,,363472,CN204698,,,,,,,,
mondo:0018192,paratesticular adenocarcinoma,"['adenocarcinoma of the paratestis', 'adenocarcinoma of paratestis']",,,363478,,,,,,,,,
mondo:0018193,testicular teratoma,"['teratoma of the testis', 'teratoma of testis', 'testicular teratoma', 'testicular teratoma (disease)']",,,363483,,,C3877,1000573,,,,,0100616
mondo:0018197,"mitochondrial DNA depletion syndrome, hepatocerebrorenal form","['mtDNA depletion syndrome, hepatocerebrorenal form']",,,363534,CN204706,,,,,,,,
mondo:0018198,acute encephalopathy with biphasic seizures and late reduced diffusion,"['acute infantile encephalopathy predominantly affecting the frontal lobes', 'AIEF', 'AESD']",,,363549,,,,,,,,,
mondo:0018199,new-onset refractory status epilepticus,"['De novo cryptogenic refractory multifocal febrile status epilepticus', 'New onset refractory status epilepticus', 'Norse']",,,363558,,,,,,,,,
mondo:0018201,extragonadal germ cell tumor,"['primary extragonadal germ cell tumor', 'tumor of extragonadal germ cell', 'primary extragonadal germ cell tumour', 'neoplasm of extragonadal germ cell', 'extragonadal germ cell tumor', 'tumour of the extragonadal germ cell', 'extragonadal germ cell neoplasms', 'neoplasm of the extragonadal germ cell', 'extragonadal germ cell neoplasm', 'tumour of extragonadal germ cell', 'tumor of the extragonadal germ cell']",,,363579,CN204711,,C3918,,,,,,
mondo:0018202,gonadal germ cell tumor,,,,363582,CN204712,,,,,,,,
mondo:0018203,LMNA-related cardiocutaneous progeria syndrome,['LCPS'],,,363618,CN204714,,,,,,,,
mondo:0018204,20q11.2 microduplication syndrome,['dup(20)(q11.2)'],,,363659,CN204718,,,,,,,,
mondo:0018205,distal monosomy 1q,"['distal monosomy type 1q', 'monosomy 1qter', 'distal deletion 1q', 'telomeric deletion 1q']",,,36367,C4273897,,,,,,,,
mondo:0018206,childhood-onset autosomal recessive myopathy with external ophthalmoplegia,,,,363677,,,,,,,,,
mondo:0018207,2p13.2 microdeletion syndrome,['Del(2)(p13.2)'],,,363680,CN204723,,,,,,,,
mondo:0018208,neurofibromatosis type 1 due to NF1 mutation or intragenic deletion,['Von Recklinghausen disease due to NF1 mutation or intragenic deletion'],,,363700,CN204726,"['0.3335', '0.501', '0.2347', '-0.4897', '0.7207', '-0.1782', '-0.10846', '0.819', '-1.0205', '-0.1707', '-0.05585', '0.11414', '0.259', '0.503', '0.001548', '-0.1032', '0.2852', '0.408', '-0.3687', '0.04684', '-0.4302', '-0.553', '-0.042', '0.26', '-0.231', '-0.4116', '-0.3135', '-0.707', '0.4802', '0.4067', '0.4827', '-0.8687', '0.174', '0.0882', '-0.6333', '-0.2029', '-0.6934', '0.16', '0.2227', '-0.2289', '0.2913', '0.3518', '0.1863', '-0.0792', '0.4875', '-0.06573', '-0.196', '0.1215', '1.25', '-0.2175', '0.07446', '0.559', '-0.01127', '0.0867', '0.3896', '0.4211', '0.01851', '0.4543', '-0.394', '-0.07776', '-0.6562', '-0.1478', '-0.3274', '-0.2654', '-0.1678', '1.003', '0.2551', '0.8496', '-0.5366', '0.9805', '0.6177', '0.1632', '0.03833', '-0.9966', '0.591', '-0.343', '-0.3718', '1.045', '0.1492', '-0.1877', '-0.1002', '0.1266', '0.478', '0.2402', '-0.5713', '-0.817', '0.537', '0.663', '0.6006', '0.5303', '-0.887', '0.4202', '-0.5483', '-0.959', '0.669', '0.0765', '0.5054', '-0.324', '0.0538', '0.569']",,,,,,,
mondo:0018209,Alexander disease type I,['AxD type I'],,,363717,CN204729,,,,,,,,
mondo:0018210,Alexander disease type II,['AxD type II'],,,363722,CN204730,,,,,,,,
mondo:0018211,Balint syndrome,"['psychic paralysis of visual fixation', 'Balint-Holmes syndrome', 'optic ataxia-gaze apraxia-simultanagnosia syndrome']",,,363746,C0270706,,,,,,,,
mondo:0018212,familial cervical artery dissection,"['hereditary cervical artery dissection', 'familial CAD', 'hereditary CAD']",,,36382,CN204734,,,,,,,,
mondo:0018213,hereditary sensory and autonomic neuropathy type 1,"['neuropathy hereditary sensory and autonomic type 1', 'HSN1', 'HSAN1', 'neuropathy hereditary sensory radicular, autosomal dominant', 'HSAN 1', 'hereditary sensory and autonomic neuropathy type I', 'hereditary sensory neuropathy type 1']",0070162,,36386,,"['0.847', '-0.01104', '-0.3145', '0.608', '-0.10815', '-0.4438', '-0.1152', '0.4658', '-0.585', '0.09125', '-0.02408', '0.5845', '0.1962', '0.778', '-0.8022', '0.367', '-0.1703', '0.805', '-0.504', '-0.7695', '0.253', '0.04526', '-0.1886', '0.662', '0.3171', '0.1143', '-0.5293', '0.0774', '-0.316', '-0.3752', '0.4863', '-0.038', '0.04022', '-0.1597', '-0.2153', '-0.5835', '0.2888', '0.0402', '-0.01611', '-0.1769', '-0.817', '-0.2866', '-0.000749', '-0.3066', '0.507', '-0.5645', '0.2474', '0.08417', '0.3455', '0.2742', '-0.2595', '0.88', '0.142', '-0.9907', '-0.005157', '0.1945', '0.52', '0.1137', '-0.1593', '-0.5894', '0.4263', '0.4329', '0.253', '0.3008', '-0.303', '0.655', '0.4788', '0.605', '0.007256', '0.11206', '-0.8613', '-0.1261', '-0.1764', '-0.0019245', '0.9004', '0.3245', '0.3582', '0.6396', '-0.4023', '0.5854', '0.01098', '-0.8145', '0.3323', '0.2252', '0.07007', '0.305', '0.5225', '-0.083', '0.4329', '-0.3848', '0.2698', '0.05847', '0.5215', '-0.1603', '0.915', '0.742', '-0.01758', '-0.1035', '0.5166', '0.1501']",,,,,,,
mondo:0018214,generalized epilepsy with febrile seizures plus,"['generalized epilepsy with febrile seizures-plus', 'genetic epilepsy with febrile seizures-plus', 'GEFS+', 'generalised epilepsy with febrile seizures-plus', 'genetic epilepsy with febrile seizures plus', 'epilepsy, generalized, with febrile seizures plus']",0060170,,36387,C3502809,"['0.677', '0.2198', '-0.663', '-0.10754', '-0.655', '-0.3394', '0.9707', '0.5195', '-0.277', '-0.4846', '0.1755', '0.709', '-0.0726', '0.2325', '-0.5576', '-0.126', '-0.2659', '-0.3047', '-0.2546', '-0.661', '0.4214', '-0.02563', '0.06223', '-0.02255', '-0.1148', '0.0786', '-0.8706', '-0.2067', '-0.4482', '-0.0841', '0.4075', '-0.6646', '-0.06235', '0.668', '-0.643', '0.2135', '-0.511', '-0.2032', '-0.06696', '-0.617', '0.4338', '-0.5728', '0.4033', '-0.3027', '0.3845', '-0.2188', '-0.757', '-0.1891', '-0.2261', '0.4446', '-0.567', '0.03992', '-0.05847', '0.2751', '0.1686', '-0.1052', '-0.2163', '0.589', '0.03772', '0.6255', '-0.509', '0.527', '0.9634', '0.4302', '-0.1178', '0.578', '0.7173', '-0.1309', '-0.719', '0.569', '0.521', '0.5645', '0.375', '-0.299', '0.1752', '1.052', '0.1681', '-0.4172', '0.507', '-0.04514', '0.1753', '0.552', '-0.5425', '0.1688', '0.1669', '0.2808', '0.1552', '0.2069', '-0.1459', '0.655', '0.2301', '0.951', '-0.01642', '-0.1938', '0.385', '0.425', '0.746', '-0.3748', '0.2563', '-0.719']",C122811,,C565808,,,,
mondo:0018215,paraneoplastic neurologic syndrome,"['PNS', 'paraneoplastic syndrome of nervous system', 'nervous system paraneoplastic syndrome', 'paraneoplastic cerebellar degeneration', 'PCD']",,,36388,,,,,,331.89,,10072106,
mondo:0018216,Koolen-de Vries syndrome due to 17q21.31 microdeletion syndrome,"['17q21.31 recurrent microdeletion syndrome', 'monosomy 17q21.31', 'Del(17)(q21.31)']",0070076,,363958,CN204740,,,,C566476,,,,
mondo:0018217,Koolen-de Vries syndrome due to a point mutation,,,,363965,CN204741,,,,,,,,
mondo:0018218,autosomal recessive cerebral atrophy,,,,363969,CN204742,,,,,,,,
mondo:0018221,immune hydrops fetalis,"['immune fetal hydrops', 'IHF', 'immune foetal hydrops', 'immune fetal edema', 'immune foetal oedema', 'immune HF']",,,364013,C0455990,,C111904,,,773.3,,,
mondo:0018222,X-linked intellectual disability due to GRIA3 anomalies,,,,364028,,"['-0.3948', '-0.1017', '0.722', '-0.383', '0.02834', '-0.3103', '-0.02869', '0.4233', '-0.4084', '-0.127', '-0.1621', '-0.0711', '0.1604', '-0.1693', '-0.1548', '0.1686', '0.37', '-0.099', '-0.2246', '-0.539', '0.1488', '0.1613', '0.1852', '-0.1818', '0.06113', '-0.2256', '-0.1733', '-0.246', '0.3528', '-0.2039', '0.1438', '-0.002558', '0.4563', '0.4111', '0.09393', '-0.1934', '-0.3286', '-0.1957', '-0.00997', '-0.4155', '0.1766', '-0.1823', '-0.2247', '0.0968', '-0.01582', '-0.5386', '0.1713', '0.0804', '-0.3228', '0.2585', '-0.3018', '0.3552', '-0.3665', '-0.01912', '0.05145', '-0.1688', '-0.03001', '-0.1823', '-0.11804', '-0.1615', '0.0022', '0.1371', '-0.4146', '0.2524', '0.091', '-0.007965', '0.1031', '0.4517', '-0.1943', '0.3699', '-0.5127', '0.2329', '0.006157', '-0.2167', '-0.1656', '0.03336', '0.3206', '-0.1667', '-0.289', '-0.1442', '-0.03357', '0.0673', '-0.1226', '0.517', '0.1853', '0.3103', '-0.2043', '0.1912', '0.1565', '0.1969', '-9.72e-05', '0.4382', '-0.086', '0.10834', '0.2974', '0.251', '0.1355', '-0.3154', '0.5386', '0.4314']",,,,,,,
mondo:0018223,systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood,"['systemic EBV-positive T-cell lymphoproliferative disease of childhood', 'EBV-positive T-cell lymphoproliferative disorder of childhood', 'systemic EBV-positive T-cell lymphoma of childhood', 'systemic EBV-positive T-cell lymphoproliferative disorder of childhood', 'systemic EBV+ T-cell LPD of childhood']",0070324,,364033,CN204753,,C80374,,,,,,
mondo:0018224,hydroa vacciniforme-like lymphoma,"['angiocentric cutaneous T-cell lymphoma of childhood', 'hydroa vacciniforme-like cutaneous T-cell lymphoma', 'hydroa vacciniforme-like lymphoma', 'hV-like lymphoma', 'HVLL', 'hydroa vacciniforme-like lymphoproliferative disorder', 'hydroa-like cutaneous T-cell lymphoma']",,,364039,C1708397,,C45327,,,,,,
mondo:0018225,ALK-positive large B-cell lymphoma,"['ALK+ LBCL', 'ALK+ large B-cell lymphoma', 'ALK-DLBCL', 'ALK-positive large B-cell lymphoma', 'diffuse large B-cell lymphoma with expression of full-length anaplastic lymphoma kinase', 'diffuse large B-cell lymphoma with expression of full-length ALK']",,,364043,C1333294,,C7225,,,,,,
mondo:0018226,infantile epileptic-dyskinetic encephalopathy,,,,364063,,"['0.1881', '0.651', '0.2385', '-0.2357', '-0.2983', '-0.8594', '0.4797', '0.4639', '-0.2483', '-0.2101', '-0.5503', '0.1732', '0.0783', '-0.2827', '0.0788', '-0.11005', '0.1421', '-0.3994', '-0.0451', '-0.7886', '0.00975', '0.04745', '0.0778', '-0.0235', '0.1126', '-0.1029', '0.1896', '-0.06696', '-0.4832', '0.03091', '0.001318', '0.1516', '0.431', '0.02419', '-0.02681', '0.4326', '-0.1349', '-0.1903', '-0.541', '0.09766', '0.1165', '-0.531', '0.1345', '0.08813', '-0.1399', '-0.03012', '-0.4238', '0.1047', '-0.11316', '0.3975', '-0.2427', '0.3103', '0.03021', '-0.1716', '0.2361', '-0.011055', '0.2001', '-0.0443', '-0.0662', '0.2307', '0.0628', '0.0044', '0.2043', '-0.1549', '-0.07184', '0.02959', '0.4385', '0.11664', '-0.3083', '0.1838', '0.1353', '-0.0502', '0.1732', '-0.2468', '-0.1097', '-0.04102', '0.537', '0.01915', '-0.4956', '0.02582', '-0.0619', '0.2834', '-0.375', '0.1434', '0.4653', '0.08716', '-0.1483', '0.5444', '0.604', '0.3523', '0.3943', '0.5', '-0.02422', '0.1148', '0.2754', '0.4124', '0.353', '-0.3987', '0.3557', '0.1426']",,,C567924,,,,
mondo:0018227,hypocomplementemic urticarial vasculitis,"['McDuffie hypocomplementemic urticarial vasculitis', 'Mac Duffie syndrome', 'McDuffie syndrome', 'Mac Duffie hypocomplementemic urticarial vasculitis', 'anti-C1q vasculitis']",,,36412,CN204757,,,,,,,,
mondo:0018228,bipartite talus,,,,364198,CN227287,,,,,,,,
mondo:0018229,Stevens-Johnson syndrome,"['Stevens Johnson syndrome', 'erythema multiforme major', 'severe cutaneous adverse reaction, susceptibility to', 'toxic Epidermal necrolysis, susceptibility to', 'hypersensitivity syndrome, carbamazepine-induced, susceptibility to', 'Stevens-Johnson syndrome, susceptibility to', 'Dermatostomatitis, Stevens Johnson type']",0050426,608579,36426,C0038325,"['0.2888', '0.4258', '-0.4753', '0.1501', '-0.2323', '0.37', '-0.286', '0.5454', '-0.539', '-0.4504', '0.5044', '-0.1648', '-0.3977', '0.3367', '-0.8994', '-0.2913', '0.07007', '0.069', '0.1396', '-0.378', '-0.11005', '0.4707', '0.2103', '-0.794', '0.03564', '-0.4023', '-0.1821', '0.2747', '0.1407', '-0.4854', '0.3037', '-0.206', '0.1417', '-0.373', '-0.2744', '0.565', '-0.3862', '-0.5996', '0.01808', '-0.003513', '-0.2306', '-0.408', '0.27', '-0.1111', '0.184', '-0.1263', '-0.01624', '-0.517', '0.3652', '0.548', '-0.3848', '-0.3557', '0.778', '-0.2695', '0.1268', '-0.3472', '0.3728', '0.643', '-0.2517', '-1.003', '0.1334', '-0.09155', '-0.3052', '0.4436', '0.337', '0.2118', '0.5024', '0.1327', '-0.3604', '0.791', '-0.2944', '0.01813', '0.1052', '-0.2734', '0.2783', '0.1514', '0.2517', '0.4678', '0.542', '-0.02728', '-0.4985', '-0.1486', '0.138', '-0.2251', '0.306', '-0.3232', '-0.1539', '0.10693', '0.3367', '0.6294', '0.873', '0.1926', '0.1907', '0.4194', '0.2766', '0.3315', '-0.45', '-0.65', '-0.372', '0.2216']",C79484,0004276,D013262,695.15,L51.1,10042033,
mondo:0018230,skeletal dysplasia,"['primary osteodysplasia', 'primary skeletal dysplasia', 'primary bone dysplasia', 'Mendelian skeletal dysplasia']",,,364526,,,,,,,,,
mondo:0018233,otopalatodigital syndrome spectrum disorder,"['OPD spectrum disorder', 'OPSD']",0111782,,364541,C2748918,,,,,,,,
mondo:0018234,dysostosis,['dysostosis'],1934,,364559,C0013393,,C34560,,D004413,756.9,,,
mondo:0018237,acrofacial dysostosis,,0060379,,364574,C1332140,"['-0.05075', '0.08795', '0.04788', '0.011665', '0.03806', '-0.0614', '0.00249', '0.0796', '-0.04456', '-0.05917', '-0.01237', '-0.012436', '-0.02216', '-0.003304', '-0.01802', '-0.004543', '0.00476', '-0.03198', '-0.0345', '-0.1302', '-0.0007253', '-0.01628', '0.0756', '-0.015236', '0.03888', '-0.01901', '-0.02336', '-0.0369', '0.008156', '-0.0245', '0.0623', '0.007187', '0.0426', '0.00955', '0.05032', '-0.05582', '-0.004677', '-0.04205', '-0.01591', '-0.09515', '-0.006973', '-0.131', '0.0375', '-0.0348', '0.000736', '-0.05765', '-0.0597', '0.1035', '-0.01066', '0.015366', '-0.01591', '0.01242', '0.002443', '0.0003917', '-0.0382', '-0.04364', '0.03107', '-0.01845', '-0.05753', '0.0096', '0.0313', '0.0313', '-0.02054', '0.01653', '-0.0001662', '-0.02364', '0.06174', '0.0719', '-0.05316', '0.03967', '-0.06836', '0.00426', '0.04718', '-0.0437', '0.014015', '0.0661', '0.0009103', '-0.03522', '-0.0612', '-0.05667', '0.00814', '-0.03111', '-0.02238', '0.1075', '0.0024', '-0.001523', '-0.01356', '0.07574', '0.0573', '0.01826', '0.00441', '0.06146', '0.00912', '0.04364', '0.1459', '0.05106', '0.06033', '-0.1242', '0.02377', '0.02213']",C35795,,,,,,
mondo:0018239,aggrecan-related bone disorder,,,,364817,CN227289,,,,,,,,
mondo:0018240,TRPV4-related bone disorder,,,,364820,CN227290,,,,,,,,
mondo:0018241,primary short bowel syndrome,,,,365563,CN204780,,,,,,,,
mondo:0018242,autoimmune hypoparathyroidism,"['autoimmune hypoparathyroidism (disease)', 'autoimmune hypoparathyroidism']",,,36913,C0271865,,,,,,,,0011771
mondo:0018243,intellectual disability-hyperkinetic movement-truncal ataxia syndrome,,,,369847,CN204803,"['-0.2793', '-0.434', '0.2218', '0.0189', '-0.03732', '-0.919', '0.3032', '-0.04337', '-0.5205', '-0.864', '0.08997', '0.2367', '-0.10913', '0.165', '0.409', '-0.3723', '-0.1301', '-0.3345', '0.012726', '-1.003', '-0.0666', '-0.2374', '0.2134', '-0.2432', '0.4844', '-0.7544', '-0.1936', '0.06946', '-0.1156', '-0.7354', '0.0666', '0.485', '-0.5034', '-0.2109', '0.3533', '0.1431', '-0.3394', '0.05402', '0.3103', '0.1819', '0.2471', '0.1672', '-0.4644', '0.4832', '0.513', '-0.4062', '0.31', '0.4683', '0.1466', '-0.03735', '-0.2527', '0.0677', '0.1937', '-0.4531', '-0.1254', '-0.6978', '0.19', '0.539', '0.0823', '0.576', '-0.244', '0.1824', '0.3452', '-0.2413', '-0.4617', '0.56', '0.228', '0.564', '-0.6772', '0.4114', '0.828', '0.507', '0.1112', '-0.514', '0.786', '0.4019', '0.3457', '0.2524', '0.2391', '0.3792', '-0.2', '-0.5806', '0.1001', '0.6753', '-0.32', '-0.386', '0.1426', '-0.1681', '0.3823', '0.6875', '0.295', '0.531', '-0.002575', '0.2468', '0.9736', '0.953', '0.3945', '0.3281', '-0.312', '-0.1726']",,,,,G71.0,,
mondo:0018244,obesity due to SIM1 deficiency,,,,369873,,,,,,,,,
mondo:0018245,2p21 microdeletion syndrome without cystinuria,['Del(2)(p21) without cystinuria'],,,369881,CN204807,,,,,,,,
mondo:0018246,homozygous 2p21 microdeletion syndrome,['2p21 contiguous gene deletion syndrome'],,,369886,CN204808,,,,,,,,
mondo:0018247,CADDS,"['Zellweger-like contiguous gene deletion syndrome', 'CADDS', 'contiguous ABCD1 DXS1357E deletion syndrome']",,,369942,CN180200,"['-0.3342', '0.0513', '0.3208', '-0.279', '0.10895', '-0.1873', '0.003838', '0.561', '-0.2225', '0.1165', '-0.3628', '-0.3584', '-0.00664', '-0.11707', '-0.4148', '-0.3057', '0.252', '-0.0628', '-0.2864', '-0.4827', '0.08673', '-0.2827', '0.2106', '-0.0663', '0.01582', '-0.2328', '-0.0742', '0.1111', '-0.0499', '-0.3142', '0.3386', '0.2874', '0.48', '0.09705', '-0.1906', '-0.1311', '-0.3254', '-0.225', '-0.1842', '-0.1797', '0.1925', '-0.2048', '0.08997', '0.10736', '-0.2703', '-0.1192', '0.2168', '0.0905', '-0.035', '0.2642', '0.04453', '0.09393', '0.0332', '-0.2085', '-0.2352', '-0.0714', '0.1052', '-0.06793', '-0.1932', '0.4045', '0.09973', '-0.02875', '0.02235', '-0.00796', '-0.03683', '-0.1436', '0.3115', '0.256', '-0.5156', '0.1813', '-0.231', '0.43', '0.0906', '0.0355', '-0.1593', '-0.06775', '0.5576', '-0.3147', '-0.1268', '0.0941', '0.1113', '0.084', '-0.2954', '0.1842', '-0.06964', '0.1959', '0.10126', '0.1313', '0.4778', '0.1421', '0.33', '0.3848', '-0.1376', '0.2012', '0.2439', '0.4438', '0.2837', '-0.0754', '0.316', '0.1991']",,,,,,,
mondo:0018248,intellectual disability-seizures-macrocephaly-obesity syndrome,['Der(8)t(8;12)'],,,369950,CN204818,"['-0.2607', '0.588', '0.0791', '0.6284', '-0.2935', '-0.794', '0.2832', '0.6646', '-0.2844', '-0.5645', '0.00955', '0.2211', '0.2423', '0.10736', '-0.765', '-0.4194', '-0.2695', '0.994', '-0.5874', '-0.834', '0.1092', '-0.1387', '0.142', '-0.2854', '0.2043', '0.2434', '-0.4226', '-0.5063', '0.2573', '-0.447', '0.374', '-0.588', '0.531', '-0.00962', '-0.1417', '-0.3706', '-0.815', '0.1005', '0.4624', '-0.0285', '0.1853', '-0.1338', '-0.9434', '0.4417', '0.2207', '-0.4968', '0.776', '0.0823', '0.419', '-0.0449', '-0.4873', '0.06058', '0.3364', '-0.2825', '-0.2285', '0.2832', '-0.5205', '-0.131', '-0.03787', '-0.364', '0.2252', '0.3906', '-0.2046', '-0.583', '-0.00933', '0.534', '-0.4014', '0.3352', '0.4663', '0.6167', '0.1743', '0.6953', '0.0915', '0.02156', '0.3975', '-0.605', '0.09235', '-0.324', '-1.368', '0.458', '-0.0665', '0.9663', '-0.02739', '0.09454', '1.02', '0.747', '0.11993', '0.1901', '0.9507', '0.447', '-0.3477', '0.5312', '-0.2057', '0.8096', '0.651', '-0.01575', '-0.02213', '-0.366', '-0.1309', '0.02313']",,,,,,,
mondo:0018249,finger hyperphalangy - toe anomalies - severe pectus excavatum syndrome,,,,369979,CN204822,,,,,,,,
mondo:0018250,diffuse palmoplantar keratoderma with painful fissures,,,,369999,CN204824,,,,,,,,
mondo:0018252,focal palmoplantar keratoderma with joint keratoses,,,,370002,CN204827,,,,,,,,
mondo:0018253,intellectual disability-facial dysmorphism-hand anomalies syndrome,,,,370010,CN204829,"['-0.2318', '0.1351', '0.3914', '-0.4023', '-0.02428', '-0.3347', '0.1733', '0.3457', '-0.3323', '-0.3118', '0.014656', '0.03128', '0.2336', '-0.1108', '-0.1792', '0.06107', '0.299', '-0.02168', '-0.2418', '-0.55', '0.077', '0.1923', '0.2155', '-0.07166', '0.3357', '-0.1395', '-0.2028', '0.04355', '0.287', '-0.3052', '0.2537', '-0.04538', '0.3403', '0.3804', '0.297', '-0.1918', '-0.0706', '-0.294', '-0.1316', '-0.552', '0.2449', '-0.2764', '-0.1318', '-0.07556', '0.1749', '-0.3628', '0.05307', '0.4688', '-0.1985', '-0.2219', '-0.4456', '0.1952', '-0.2073', '0.0958', '-0.2622', '-0.2146', '-0.1111', '-0.1794', '-0.147', '0.1119', '0.0899', '0.02437', '-0.3018', '0.2104', '-0.1638', '0.01648', '0.0486', '0.2142', '-0.11383', '0.252', '-0.4333', '0.1821', '0.1525', '-0.11536', '-0.1714', '0.03366', '0.1274', '-0.4536', '-0.1879', '0.02367', '0.1012', '0.0631', '0.0555', '0.6724', '0.1536', '0.297', '-0.2676', '0.379', '0.301', '0.1752', '-0.0009575', '0.3647', '0.1659', '0.1831', '0.6606', '-0.0943', '0.2922', '-0.3804', '0.368', '0.2812']",,,,,,,
mondo:0018254,"spondyloepimetaphyseal dysplasia, Isidor type",,,,370015,,,,,,,,,
mondo:0018255,"spondylometaphyseal dysplasia, Czarny-Ratajczak type",,,,370019,,,,,,,,,
mondo:0018256,acute myeloid leukemia with t(8;16)(p11;p13) translocation,['AML with t(8;16)(p11;p13) translocation'],,,370026,CN204831,,,,,,,,
mondo:0018257,familial syringomyelia,['hereditary syringomyelia'],,,370034,CN204832,,,,,,,,
mondo:0018258,Angora hair nevus,['Schauder syndrome'],,,370039,CN204833,,,,,,,,
mondo:0018259,didymosis aplasticosebacea,['aplasia cutis congenita-nevus sebaceus syndrome'],,,370046,CN204834,,,,,,,,
mondo:0018260,scalp syndrome,"['sebaceous nevus-CNS malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome', 'sebaceous nevus-central nervous system malformations-aplasia cutis congenital-limbal dermoid-pigmented nevus syndrome']",,,370052,,,,,,,,,
mondo:0018261,Nevada syndrome,['Nevus epidermicus verrucosus with angiodysplasia and aneurysms'],,,370059,CN204836,,,,,,,,
mondo:0018262,fetal anticonvulsant syndrome,"['fetal AEDS', 'foetal antiepileptic drug syndrome', 'foetal AEDS', 'fetal antiepileptic drug syndrome', 'FACS']",,,370068,C1739111,,,,,,,,
mondo:0018263,fetal carbamazepine syndrome,,,,370076,CN204839,,,,,760.8,,,
mondo:0018264,oculocutaneous albinism type 6,"['OCA6', 'albinism, oculocutaneous, type VI', 'skin/hair/eye pigmentation 4, fair/dark skin']",0080614,113750,370097,C3805375,"['0.3047', '0.1318', '-0.1987', '0.3828', '0.6064', '-0.1766', '-0.535', '0.4255', '-0.5933', '-0.674', '0.535', '-0.3645', '-0.03738', '1.021', '-0.1636', '0.4487', '0.5337', '0.02771', '0.2263', '-0.6445', '-1.129', '0.2476', '0.6436', '-0.5273', '-0.11206', '-0.1478', '-0.8867', '-0.03854', '0.721', '0.04214', '0.4336', '0.1759', '0.3057', '0.6094', '0.0237', '0.5', '-0.9595', '-0.7334', '0.1109', '-0.3489', '1.401', '-0.2079', '-0.3594', '-0.1962', '-0.4387', '-0.726', '0.6997', '-1.034', '0.891', '0.384', '-0.0588', '-0.4814', '0.415', '-0.1526', '0.5684', '0.323', '0.2368', '0.9106', '0.03113', '-0.7783', '-0.2817', '0.2081', '0.6094', '0.609', '-0.3767', '0.1149', '0.377', '0.5737', '-0.352', '0.638', '-0.164', '0.4436', '-0.12415', '-0.05597', '0.779', '0.02232', '0.0796', '-0.1715', '0.3125', '0.07446', '0.663', '-0.3877', '0.4683', '0.8877', '-0.2458', '-1.575', '0.7056', '0.6626', '0.909', '0.423', '0.05', '1.152', '0.143', '-0.1738', '0.635', '0.358', '-0.3809', '-0.3108', '0.2737', '0.4546']",,,,,,,
mondo:0018266,ataxia - telangiectasia variant,['v-AT'],,,370109,C1876175,,,,,,,,
mondo:0018267,combined cervical dystonia,,,,370114,,,,,,,,,
mondo:0018268,Medich giant platelet syndrome,['Medich macrothrombocytopenia'],,,370127,CN204847,,,,,,,,
mondo:0018269,white platelet syndrome,['platelet granule deficiency disorder'],,,370131,C2931293,,,,C536702,,,,
mondo:0018270,extraskeletal Ewing sarcoma,"['extraosseous Ewing tumour', 'extraskeletal Ewing tumor', 'EOE', 'extraskeletal Ewing sarcoma', 'extraosseous Ewing^s tumor', 'Extra-osseous Ewing^s sarcoma', 'extraskeletal Ewing tumour', 'extraosseous Ewing sarcoma', 'extraskeletal Ewing^s sarcoma', 'extraosseous Ewing tumor', 'extraosseous Ewing^s sarcoma', 'extraosseous Ewing^s sarcoma/peripheral primitive neuroectodermal tumour', 'extraosseous Ewing^s tumour']",4232,,370334,CN204849,,C7135,,,,,,
mondo:0018271,peripheral primitive neuroectodermal tumor,"['PPNET', 'peripheral PNET', 'pPNET', 'peripheral neuroectodermal tumor', 'peripheral neuroepithelioma', 'peripheral primitive neuroectodermal tumor', 'peripheral neuroectodermal tumour', 'peripheral primitive neuroectodermal neoplasm', 'peripheral neuroectodermal neoplasm']",,,370348,C3489398,,C9341,,,,,,
mondo:0018273,XYLT1-congenital disorder of glycosylation,"['XYLT18-CDG', 'XYLT1-CDG - xylosyltransferase 1 congenital disorder of glycosylation']",,,370930,CN204859,,,,,,,,
mondo:0018274,GM3 synthase deficiency,"['ST3GAL5-CDG', 'infantile-onset symptomatic epilepsy syndrome-developmental stagnation-blindness syndrome', 'infantile-onset symptomatic epilepsy syndrome - developmental stagnation - blindness', 'salt and pepper mental retardation syndrome', 'epilepsy syndrome, infantile-onset symptomatic', 'Amish infantile epilepsy syndrome', 'SPDRS', 'salt & pepper syndrome', 'disorder of lactosylceramide alpha-2,3-sialyltransferase activity', 'salt and pepper developmental regression syndrome', 'salt-and-pepper syndrome', 'lactosylceramide alpha-2,3-sialyltransferase activity disease']",0060470,609056,370938,CN204860,"['-0.2307', '0.7056', '-0.1731', '-0.04846', '-0.0993', '-0.6523', '0.0006695', '0.289', '-0.265', '-0.5376', '-0.03937', '-0.0697', '0.1721', '0.1973', '0.2201', '-0.05194', '0.3855', '0.05923', '-0.4238', '-0.3572', '0.3347', '0.04688', '0.05737', '-0.13', '0.306', '-0.2087', '0.0255', '-0.2186', '-0.6924', '0.4836', '0.2864', '-0.1667', '-0.001312', '0.01813', '-0.1249', '0.3293', '0.106', '0.2174', '-0.06934', '0.3364', '0.1522', '-0.7275', '-0.3772', '0.475', '-0.4236', '0.1923', '0.0526', '-0.3591', '0.1531', '0.652', '-0.0707', '-0.01558', '0.3494', '-0.01548', '-0.04883', '0.46', '0.321', '0.2053', '-0.433', '0.532', '-0.05942', '0.03001', '0.04428', '0.02309', '-0.1365', '-0.1567', '0.6074', '-0.1043', '-0.2517', '0.583', '0.2854', '0.6733', '-0.2773', '-0.2283', '0.1073', '-0.1764', '0.274', '-0.2122', '-0.2075', '0.11206', '0.0002016', '-0.08453', '-0.01755', '-0.1621', '-0.2355', '-0.3098', '0.356', '0.728', '0.655', '0.6597', '0.238', '0.2769', '-0.11896', '0.02867', '-0.0252', '0.4407', '0.1362', '-0.4805', '0.5586', '0.2294']",,,,,,,
mondo:0018276,muscular dystrophy-dystroglycanopathy,"['CMD due to dystroglycanopathy', 'congenital muscular dystrophy due to dystroglycanopathy']",0112374,,370953,CN229783,,,,,,,,
mondo:0018277,congenital muscular dystrophy with cerebellar involvement,"['CMD with cerebellar involvement', 'CMD-CRB']",,,370959,,,,,,,,,
mondo:0018278,congenital muscular dystrophy with intellectual disability,"['CMD with intellectual disability', 'CMD-MR']",,,370968,,,,,,,,,
mondo:0018279,congenital muscular dystrophy without intellectual disability,"['CMD without intellectual disability', 'CMD-no MR', 'congenital muscular dystrophy-dystroglycanopathy without intellectual disability']",,,370980,,,,,,,,,
mondo:0018280,muscle-eye-brain disease with bilateral multicystic leucodystrophy,['MEB disease with bilateral multicystic leucodystrophy'],,,370997,,,,,,,,,
mondo:0018281,congenital muscular dystrophy with hyperlaxity,['CMDH'],,,371007,,,,,,,,,
mondo:0018282,qualitative or quantitative defects of alpha-dystroglycan,"['alpha-dystroglycanopathy', 'dystroglycanopathy']",,,371024,,,,,,,,,
mondo:0018283,primary qualitative or quantitative defects of alpha-dystroglycan,"['primary dystroglycanopathy', 'primary alpha-dystroglycanopathy']",,,371040,,,,,,,,,
mondo:0018292,congenital disorder of glycosylation-related bone disorder,['CDG-related bone disorder'],,,371195,,,,,,,,,
mondo:0018298,multicentric osteolysis-nodulosis-arthropathy spectrum,['mona spectrum'],,,371428,CN227313,,,,,,,,
mondo:0018301,interstitial cystitis,"['chronic interstitial cystitis', 'interstitial cystitis/bladder pain syndrome', 'IC/BPS', 'IC/PBS', 'interstitial cystitis/painful bladder syndrome', 'ulcerative cystitis', 'interstitial cystitis, chronic', 'painful bladder syndrome', 'bladder pain syndrome']",1678,,37202,CN204884,,C27189,1000869,D018856,595.1,,10011796,
mondo:0018302,acquired kinky hair syndrome,,,,37559,CN204889,,,,,,,,
mondo:0018304,Schnitzler syndrome,"['chronic urticaria with gammopathy', 'chronic urticaria with gammapathy', 'chronic urticaria with macroglobulinemia']",4371,,37748,C0524988,,,1001165,D019873,708.8,,10062908,
mondo:0018305,chronic granulomatous disease,"['chronic septic granulomatosis', 'congenital dysphagocytosis', 'CGD', 'granulomatous disease, chronic', 'Quie syndrome', 'Bridges-Good syndrome']",3265,,379,C0018203,"['0.2473', '0.2039', '-0.2812', '-0.1902', '0.3564', '0.006172', '0.2494', '0.1638', '-0.3618', '0.0193', '0.2299', '-0.3032', '-0.637', '0.6177', '-0.3892', '0.06287', '-0.7393', '-0.0667', '-0.704', '-0.5225', '-0.3962', '-0.424', '0.5117', '-0.3127', '-0.1598', '-0.0726', '-0.28', '0.1592', '0.01146', '-0.5303', '0.058', '-0.0271', '0.0788', '-0.10065', '0.3848', '0.3176', '-0.675', '-0.07104', '0.32', '-0.1173', '0.3462', '-0.1482', '0.1509', '-0.4316', '-0.2776', '0.1588', '-0.6357', '-0.775', '0.398', '0.8013', '0.2339', '-0.2047', '0.9814', '-0.2283', '0.03174', '0.01843', '-0.2527', '0.42', '-0.03894', '-0.1284', '0.07495', '0.546', '-0.3145', '0.4316', '0.6475', '0.02534', '0.626', '0.332', '0.02792', '0.6704', '-0.09937', '-0.3323', '-0.0955', '0.03061', '0.537', '0.4626', '0.2325', '-0.03516', '0.4668', '0.2423', '-0.3125', '-0.4944', '0.5186', '-0.4731', '-0.2822', '0.0933', '1.099', '0.2817', '0.1016', '-0.1053', '0.1576', '0.4934', '-0.2343', '-0.4106', '0.648', '0.4883', '-0.3457', '-0.803', '0.1493', '-0.181']",C26788,,D006105,,,10008906,
mondo:0018306,Griscelli syndrome,"['Griscelli disease', 'Griscelli-PruniC)ras syndrome', 'Griscelli-Pruniéras syndrome', 'partial albinism-immunodeficiency syndrome', 'Ch��diak-Higashi-like syndrome', 'ChC)diak-Higashi-like syndrome', 'Griscelli-Pruni��ras syndrome', 'Chédiak-Higashi-like syndrome']",0060831,,381,CN204933,"['0.276', '0.1946', '-0.03848', '-0.2908', '0.04196', '-0.3381', '0.1152', '0.2465', '-0.4258', '0.2705', '-0.2183', '-0.2585', '-0.4094', '0.07074', '-0.05545', '-0.5356', '0.3223', '0.1074', '-0.0575', '-0.7314', '0.1372', '-0.2761', '0.994', '-0.276', '0.03647', '-0.01138', '-0.2458', '0.3423', '-0.6123', '-0.063', '1.1455', '0.2281', '0.3708', '0.08276', '0.3147', '-0.1981', '-0.2917', '0.1974', '0.1349', '0.05344', '0.603', '-0.353', '-0.1186', '-0.2306', '-0.822', '-0.05798', '-0.2102', '-0.2715', '0.1499', '-0.7734', '0.1863', '-0.282', '0.6284', '0.254', '-0.2281', '0.6885', '0.77', '-0.7534', '-0.1758', '0.3308', '-0.4023', '-0.10333', '0.1775', '-0.2053', '0.01784', '0.05563', '-0.3142', '0.2255', '0.02124', '0.6475', '-0.553', '-0.2267', '-0.7207', '0.2874', '0.2522', '-0.2163', '-0.3984', '0.07184', '-0.4333', '0.0734', '0.006557', '-0.74', '-0.07214', '0.2417', '-0.2416', '-0.6074', '0.6357', '1.006', '0.5317', '0.5024', '0.506', '0.669', '0.11194', '-0.35', '0.6475', '0.086', '-0.2595', '-0.5635', '0.4822', '0.162']",,,,270.2,E70.3,,
mondo:0018307,neurodegeneration with brain iron accumulation,['NBIA'],0110734,,385,,"['-0.288', '0.529', '0.2847', '-0.323', '0.11707', '-0.711', '0.011986', '0.2954', '0.1087', '0.2313', '-0.545', '-0.4973', '-0.3835', '0.06415', '0.3374', '-0.448', '-0.1876', '-1.037', '-0.5327', '-0.7095', '0.11865', '-0.3303', '0.305', '0.141', '-0.06635', '0.0753', '0.2128', '-0.61', '-0.7764', '0.1338', '0.2471', '0.2925', '0.2229', '-0.339', '0.1904', '0.05743', '-0.3135', '-0.675', '0.15', '0.2264', '0.7363', '-0.513', '0.05264', '0.1567', '0.831', '-0.3718', '0.1278', '0.01689', '0.2417', '-0.09357', '0.6274', '0.5903', '-0.4011', '-0.4443', '-0.3096', '-0.237', '0.3328', '0.47', '-0.5464', '0.1263', '-0.0289', '0.1552', '0.5776', '-0.2455', '-0.3174', '0.2312', '0.494', '0.1964', '-0.3171', '0.2261', '-0.128', '-0.5244', '0.08215', '0.04874', '0.6924', '0.652', '-0.1062', '-0.134', '-0.413', '-0.3276', '0.445', '-0.735', '-0.659', '0.2935', '0.4333', '-0.5635', '0.54', '0.1985', '0.235', '-0.1393', '0.2524', '-0.0791', '-0.0219', '0.2145', '0.2203', '0.775', '0.5312', '0.2207', '0.1455', '-0.01929']",,,C538421,,,,
mondo:0018308,liver mesenchymal hamartoma,"['mesenchymal hamartoma of liver', 'Von Meyenburg complexes disease', 'biliary hamartoma', 'VMC', 'MHL', 'mesenchymal hamartoma of the liver', 'liver mesenchymal hamartoma', 'liver MH', 'hepatic mesenchymal hamartoma', 'hepatic cystic hamartoma']",,,386,C1333971,,C5751,,,,,,
mondo:0018309,Hirschsprung disease,"['HSCR', 'congenital intestinal aganglionosis', 'congenital megacolon', 'aganglionic megacolon', 'Hirschsprung disease', 'macrocolon', 'Hirschsprung disease susceptibility', 'Hirschsprung^s disease', 'pelvirectal achalasia']",10487,,388,C3661523,"['-0.6343', '0.1755', '0.0903', '-0.0755', '-0.08734', '-0.5625', '-0.2847', '0.2896', '-0.0873', '-0.4998', '0.7173', '-0.2238', '-0.2983', '0.4893', '-0.5557', '-0.1333', '-0.5254', '-0.4697', '-0.04495', '-0.681', '0.2896', '-0.4243', '0.0392', '-0.525', '0.448', '0.001283', '0.0484', '0.2573', '0.858', '0.1906', '0.4163', '-0.4653', '-0.03047', '0.02365', '-0.4639', '0.2551', '-0.522', '0.2742', '-0.4485', '0.6753', '-0.2803', '0.2075', '0.0637', '-0.338', '0.4578', '-0.2461', '-0.4314', '-0.543', '-0.3687', '0.12067', '-0.506', '-0.04498', '0.4995', '-1.198', '0.08215', '-0.394', '-0.3096', '0.00916', '-0.421', '0.073', '0.1164', '0.1628', '0.4841', '0.02843', '0.3145', '0.38', '0.9634', '0.3604', '-0.5107', '0.3926', '-0.4358', '0.1384', '0.5728', '-0.2292', '0.04474', '-0.1576', '-0.0213', '0.12256', '0.3113', '-0.4614', '0.2335', '-0.3848', '0.1208', '-0.0651', '-0.396', '0.1509', '0.6895', '0.3948', '0.06125', '-0.6504', '-0.4294', '0.3215', '0.3406', '0.1016', '0.506', '0.01923', '0.1432', '-0.369', '0.1538', '0.2477']",C34700,,D006627,,,10010539,
mondo:0018310,Langerhans cell histiocytosis,"['letterer-Siwe disease of lymph nodes of axilla and upper limb', 'Langerhans-cell histiocytosis', 'letterer-Siwe disease of intrathoracic lymph nodes', 'letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb', 'letterer-Siwe disease of lymph nodes of head, face and neck', 'letterer-Siwe disease involving lymph nodes of inguinal region and lower limb', 'letterer-Siwe disease of lymph nodes of axilla and/or upper limb', 'letterer-Siwe disease of lymph nodes of head, face and/or neck', 'letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb', 'Lch', 'Langerhans cell histiocytosis, NOS', 'letterer-Siwe disease involving intrathoracic lymph nodes', 'letterer-Siwe disease of lymph nodes of multiple sites', 'letterer-Siwe disease involving intra-abdominal lymph nodes', 'histiocytosis X', 'Langerhans cell histiocytosis, Not otherwise specified', 'Langerhans cell granulomatosis', 'LCH', 'letterer-Siwe disease involving lymph nodes of head, face, and neck', 'Langerhan^s cell histiocytosis', 'letterer-Siwe disease involving lymph nodes of axilla and upper limb', 'letterer-Siwe disease involving spleen', 'letterer-Siwe disease of intrapelvic lymph nodes', 'letterer-Siwe disease of intra-abdominal lymph nodes', 'letterer-Siwe disease involving lymph nodes of multiple sites', 'letterer-Siwe disease of spleen', 'letterer-Siwe disease involving lymph nodes of head, face and neck', 'letterer-Siwe disease of lymph nodes of inguinal region and lower limb', 'Langerhans cell histiocytosis', 'letterer-Siwe disease involving intrapelvic lymph nodes']",2571,604856,389,C0432554,,C3107,1000318,,277.89,,10069698,
mondo:0018311,acromelanosis,['progressive acromelanosis'],,,39,,,,,,709.09,,,
mondo:0018312,histoplasmosis,"['darling disease', 'Histoplasma caused disease or disorder']",1731,,390,C0035288,,C77201,0007310,D006660,115.99,B39,10021808,
mondo:0018314,infantile-onset mesial temporal lobe epilepsy with severe cognitive regression,,,,391316,CN204956,,,,,,,,
mondo:0018315,X-linked osteoporosis with fractures,,,300910,391330,,"['0.2627', '-0.2769', '0.001913', '0.558', '0.1766', '-0.4702', '-0.7354', '0.8555', '-0.7056', '-0.3997', '0.46', '0.5137', '-0.086', '0.613', '-0.3882', '-0.2578', '-0.1849', '0.483', '-0.878', '-0.198', '-0.02667', '-0.434', '0.3162', '-0.473', '0.428', '-0.3035', '0.1901', '-0.9697', '-0.627', '-0.2637', '0.704', '-0.603', '-0.321', '-0.3735', '-0.05643', '-0.2595', '0.0293', '-0.8813', '0.3286', '-0.5986', '-0.00543', '0.0759', '0.1436', '-0.4702', '0.6167', '-0.6567', '0.1152', '0.04025', '0.3596', '0.7773', '0.661', '0.2374', '0.369', '-0.1812', '-0.546', '-0.623', '-0.3044', '0.3594', '-0.431', '0.04095', '0.422', '0.0814', '-0.943', '-0.629', '0.075', '0.839', '0.5312', '0.75', '-0.2698', '-0.51', '0.6294', '-0.1835', '-0.07764', '-0.4758', '0.599', '0.4348', '-0.1774', '0.587', '-0.10834', '0.2122', '-0.0876', '-0.4036', '0.4539', '0.585', '-0.7617', '0.604', '0.2686', '-0.08295', '1.262', '0.1826', '-0.351', '-0.1093', '-0.9824', '-0.0709', '0.5425', '-0.1707', '0.059', '-0.4275', '-0.0925', '-0.4243']",,,,,,,
mondo:0018316,fatal post-viral neurodegenerative disorder,,,,391343,CN204961,,,,,,,,
mondo:0018317,growth retardation-mild developmental delay-chronic hepatitis syndrome,,,,391366,CN204964,,,,,,,,
mondo:0018318,disorder of asparagine metabolism,,,,391381,CN227320,,,,,,,,
mondo:0018319,familial episodic pain syndrome,['FEPS'],0111728,,391384,CN228162,"['-0.1566', '-0.09015', '-0.3467', '-0.0649', '-0.0236', '-0.4148', '0.3323', '0.405', '-0.1787', '0.0696', '-0.1848', '0.1803', '0.0425', '0.2161', '-0.02855', '0.1439', '0.1333', '-0.10706', '0.02058', '-0.4717', '0.0823', '-0.053', '-0.00754', '-0.175', '-0.3975', '0.04178', '0.2286', '-0.073', '0.0808', '-0.1638', '0.2476', '0.0654', '0.05524', '0.138', '-0.004562', '-0.1774', '-0.4143', '-0.1304', '-0.02538', '-0.1189', '0.1682', '-0.0681', '0.05374', '0.372', '0.287', '-0.1797', '-0.498', '0.2795', '0.1821', '0.52', '-0.601', '0.306', '0.2395', '0.0643', '0.2429', '0.1292', '0.099', '-0.2104', '-0.1779', '-0.347', '0.03784', '0.1926', '-0.002943', '-0.2847', '-0.1432', '0.448', '0.3838', '0.4863', '0.093', '0.507', '-0.3877', '0.0332', '-0.09515', '-0.18', '0.01654', '0.3374', '0.2158', '0.274', '0.208', '-0.1168', '-0.00577', '-0.0001241', '0.463', '0.09705', '0.3774', '0.01724', '0.05536', '0.537', '0.4065', '0.09503', '0.3281', '-0.0643', '0.302', '0.2262', '0.4265', '0.2944', '0.4045', '-0.07654', '-0.3901', '0.27']",,,,,,,
mondo:0018320,primary microcephaly-mild intellectual disability-young-onset diabetes syndrome,,,,391408,CN204971,"['0.6895', '-0.2268', '0.3743', '0.5503', '-0.4475', '-0.7856', '-0.3794', '1.093', '0.1353', '-0.627', '0.1918', '-0.10785', '0.411', '-0.03427', '-0.711', '-0.2361', '0.434', '0.1489', '-0.1809', '-0.6123', '0.2996', '-0.01659', '0.00487', '-0.02104', '-0.6045', '-0.539', '0.06396', '-0.1466', '0.4756', '-0.4492', '0.9697', '-0.5186', '0.1646', '-0.3235', '-0.1692', '0.678', '-0.6987', '0.3562', '0.12213', '-0.1365', '0.2278', '0.4983', '0.0533', '0.5664', '-0.4915', '-0.3816', '0.4224', '-0.2445', '-0.007366', '0.10205', '0.2554', '-0.2761', '0.638', '-0.9497', '-0.06046', '0.3293', '-0.1525', '-1.018', '-0.824', '0.5757', '-0.4685', '0.409', '-0.06396', '0.09546', '-0.1411', '0.644', '-0.4302', '0.6777', '-1.057', '0.1157', '0.2289', '0.3523', '0.1722', '-0.1987', '0.4724', '0.3818', '-0.5405', '1.031', '-0.2391', '-0.1935', '0.04514', '0.374', '-0.11975', '-0.3906', '0.2563', '0.2603', '-0.1821', '0.4626', '0.6997', '0.2122', '0.719', '0.6045', '0.05713', '-0.1974', '1.183', '0.1521', '-0.09625', '-0.1235', '-0.1074', '0.09515']",,,,,,,
mondo:0018321,atypical juvenile parkinsonism,,,,391411,CN204972,,,,,,,,
mondo:0018322,"HSD10 disease, infantile type","['2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, infantile type', 'MHBD deficiency, infantile type', '2-methyl-3-hydroxybutyric aciduria, infantile type', 'MHBD deficiency, classic type', 'HSD10 deficiency, infantile type', '2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, classic type', 'HSD10 disease, classic type', '2-methyl-3-hydroxybutyric aciduria, classic type', 'HSD10 deficiency, classic type']",,,391428,CN204974,,,,,,,,
mondo:0018323,"HSD10 disease, neonatal type","['MHBD deficiency, neonatal type', 'HSD10 deficiency, neonatal type', '2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency, neonatal type', '2-methyl-3-hydroxybutyric aciduria, neonatal type']",,,391457,CN204975,,,,,,,,
mondo:0018324,adult-onset myasthenia gravis,"['adult-onset autoimmune myasthenia gravis', 'adult-onset acquired myasthenia']",,,391490,,,,,,,,,
mondo:0018325,juvenile myasthenia gravis,"['pediatric myasthenia gravis', 'juvenile acquired myasthenia', 'childhood myasthenia gravis', 'juvenile autoimmune myasthenia gravis', 'paediatric myasthenia gravis', 'myasthenia gravis of childhood']",,,391497,,,,,,,,,
mondo:0018326,transient neonatal myasthenia gravis,"['NMG', 'neonatal myasthenia gravis', 'transient neonatal acquired myasthenia', 'transient neonatal autoimmune myasthenia gravis']",,,391504,C0495465,,C117308,,,,P94.0,,
mondo:0018327,glomus tumor,"['glomus neoplasm', 'glomus tumor']",2431,,391651,C0017653,,C3060,,D005918,239.7,,,
mondo:0018328,homozygous familial hypercholesterolemia,['HoFH'],,,391665,,"['0.02988', '0.334', '-0.5063', '0.3262', '0.2444', '-0.6577', '-0.5176', '-0.173', '-0.3518', '-0.2756', '-0.0948', '-0.3489', '0.1394', '0.5405', '0.1445', '-1.107', '0.179', '0.2805', '-0.1182', '-0.6587', '-0.1453', '0.2566', '0.905', '0.0551', '0.2091', '0.2369', '0.02664', '0.199', '0.3916', '-0.28', '0.9946', '-0.646', '0.7046', '-0.1519', '-0.162', '0.0802', '0.4766', '0.353', '0.7056', '-1.414', '0.2625', '-0.0777', '-0.05164', '0.1537', '-0.1257', '0.03038', '0.2913', '-0.2886', '0.0754', '0.02522', '0.156', '-0.02527', '0.333', '-0.1742', '-0.4324', '-0.525', '0.11414', '0.168', '0.236', '-0.1924', '-0.248', '0.3032', '0.4377', '-0.2476', '0.2487', '0.535', '-0.1396', '0.6274', '-0.4714', '-0.1632', '-0.2766', '0.2595', '0.443', '0.1957', '-0.04205', '0.564', '-0.304', '0.711', '-0.1875', '-0.0614', '-0.7007', '0.1698', '0.0909', '0.02759', '0.3264', '0.000527', '0.5103', '-0.2432', '0.4949', '0.5557', '-0.5615', '-0.1643', '-0.2396', '0.575', '0.584', '0.4343', '0.5317', '-0.2969', '-0.523', '-0.6113']",,,D000090542,,,,
mondo:0018329,persistent combined dystonia,,,,391711,,,,,,,,,
mondo:0018330,mucinous adenocarcinoma of the appendix,"['appendix mucinous adenocarcinoma', 'appendiceal mucinous adenocarcinoma', 'vermiform appendix mucinous adenocarcinoma']",,,391723,C1706832,,C43558,,,,,,
mondo:0018332,"multiple acyl-CoA dehydrogenase deficiency, severe neonatal type","['MADD, severe neonatal type', 'glutaric aciduria type 2, severe neonatal type', 'MAD deficiency, severe neonatal type']",,,394529,CN205004,,,,,,,,
mondo:0018333,"multiple acyl-CoA dehydrogenase deficiency, mild type","['MADD, mild type', 'MAD deficiency, mild type', 'glutaric aciduria type 2, mild type']",,,394532,CN205005,,,,,,,,
mondo:0018334,chronic hiccup,"['Hiccups, intractable', 'persistent hiccups', 'intractable hiccups', 'intractable singultus', 'chronic hiccups']",,,396,CN205022,,,,,,,,0100247
mondo:0018337,severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency,,,,397593,,"['-0.381', '0.2137', '-0.09644', '-0.02217', '-0.2407', '-0.3528', '-0.05045', '0.369', '-0.166', '0.1943', '-0.2463', '-0.3262', '0.09564', '-0.0797', '-0.1083', '-0.011665', '0.0725', '-0.0432', '-0.281', '-0.6514', '-0.0693', '-0.2078', '0.6104', '0.10406', '0.08075', '0.02611', '0.086', '0.03516', '0.009735', '-0.3132', '0.10724', '0.4045', '0.702', '0.2974', '-0.3203', '-0.1892', '-0.1394', '-0.0413', '-0.3684', '0.006065', '-0.0615', '-0.4038', '0.0911', '0.267', '-0.1754', '-0.1633', '-0.03235', '0.081', '-0.1145', '0.4758', '-0.383', '-0.11676', '0.1227', '-0.2178', '-0.231', '-0.12396', '-0.03046', '-0.00947', '-0.09705', '0.3308', '0.1947', '0.09436', '0.3943', '0.003483', '-0.0991', '-0.04413', '0.4707', '0.428', '-0.4392', '0.3828', '-0.06525', '0.1595', '0.02127', '-0.1804', '-0.06525', '0.0886', '0.2517', '-0.09955', '-0.01191', '0.3735', '0.002983', '0.128', '-0.2974', '0.01242', '0.2622', '0.187', '0.2178', '0.2236', '0.4707', '-0.04974', '0.3828', '0.1698', '-0.05618', '0.04288', '0.4607', '0.746', '0.2954', '-0.2113', '0.3376', '0.1884']",,,,,,,
mondo:0018338,activated PI3K-delta syndrome,"['senescent T-cells-lymphadenopathy-immunodeficiency syndrome due to p110delta-activating mutation', 'APDS']",,,397596,C3714976,"['-0.08453', '0.264', '0.2507', '-0.5713', '-0.0741', '-0.1372', '0.1655', '-0.166', '0.1687', '0.1685', '-0.1321', '0.06076', '-0.0954', '-0.1407', '-0.0579', '-0.05176', '0.11584', '0.1637', '-0.0928', '-0.4912', '-0.003769', '-0.4128', '0.542', '-0.11896', '0.1681', '-0.02023', '-0.011116', '-0.00345', '-0.2363', '-0.4243', '0.2825', '0.2852', '0.7036', '0.06396', '0.1732', '-0.02567', '-0.705', '0.11053', '-0.3428', '-0.414', '-0.3948', '-0.2406', '0.05997', '-0.3125', '-0.1879', '-0.4434', '-0.0988', '-0.0618', '0.057', '0.162', '0.0723', '0.09784', '0.3237', '-0.006554', '-0.3767', '0.03525', '-0.03056', '-0.595', '-0.3945', '0.0719', '0.1326', '0.3425', '-0.2593', '0.0408', '0.449', '0.09955', '0.4988', '0.2913', '-0.184', '0.4055', '-0.163', '-0.3113', '0.09705', '-0.1274', '0.1207', '-0.4565', '0.2683', '0.2162', '0.2281', '-0.1436', '-0.283', '-0.03192', '0.003296', '0.1111', '-0.1539', '-0.2222', '0.316', '0.273', '0.2401', '0.01628', '0.4119', '0.385', '-0.01575', '0.1289', '0.7656', '0.7134', '0.3997', '-0.285', '-0.3438', '-0.1575']",,,C585640,279.8,,,
mondo:0018339,PrP systemic amyloidosis,"['chronic diarrhea with hereditary sensory and autonomic neuropathy', 'prion protein systemic amyloidosis', 'chronic diarrhoea with HSAN', 'chronic diarrhoea with hereditary sensory and autonomic neuropathy', 'chronic diarrhea with HSAN']",,,397606,C4518776,,,,,,,,
mondo:0018340,hereditary isolated aplastic anemia,,,,397692,,,,,,,,,
mondo:0018341,3q27.3 microdeletion syndrome,['Del(3)(q27.3)'],,,397695,CN225942,,,,,,,,
mondo:0018342,Joubert syndrome with Jeune asphyxiating thoracic dystrophy,"['Joubert syndrome with JATD', 'JBTS with JATD']",,,397715,CN225944,"['-0.8794', '0.03458', '0.632', '-0.6826', '0.005363', '-0.681', '-0.0994', '0.462', '-0.451', '-0.3186', '-0.136', '-0.865', '-0.3098', '-0.05927', '0.2499', '-0.5205', '0.2715', '0.1578', '-0.3635', '-1.217', '0.2006', '0.009735', '0.588', '-0.1831', '-0.2028', '0.2832', '-0.2769', '-0.1172', '0.2505', '-0.05573', '0.1476', '0.1682', '0.3567', '0.1536', '0.2812', '0.449', '0.2035', '0.00971', '-0.251', '-0.4827', '0.1741', '-0.411', '0.03687', '0.03418', '0.04547', '-0.2712', '0.1355', '0.33', '0.1604', '0.2114', '-0.383', '0.813', '0.263', '-0.3318', '-0.3982', '-0.6797', '0.01033', '0.0924', '0.08875', '-0.2898', '0.5586', '-0.1794', '-0.1915', '0.3164', '-0.4229', '-0.6826', '0.1777', '0.5674', '-0.3396', '0.2773', '-0.3828', '0.3752', '0.4563', '0.295', '-0.04626', '-0.1262', '0.2827', '-0.0478', '-0.10834', '0.02362', '-0.2864', '-0.04886', '-0.1503', '0.1815', '-0.245', '-0.2913', '0.3777', '0.1344', '0.2144', '0.2854', '-0.0747', '-0.3003', '-0.04523', '0.486', '0.4438', '0.3733', '0.7817', '-0.0871', '0.1538', '0.5884']",,,,,,,
mondo:0018343,periodic paralysis with later-onset distal motor neuropathy,,,,397750,,,,,,,,,
mondo:0018346,ferro-cerebro-cutaneous syndrome,"['FCCS', 'cerebro-cutaneous syndrome with iron overload']",,301072,397922,CN226080,,,,,,,,
mondo:0018347,severe intellectual disability-progressive postnatal microcephaly- midline stereotypic hand movements syndrome,"['IQSEC2-related syndromic intellectual disability', 'severe intellectual disability-progressive postnatal microcephaly-midline stereotypic hand movements syndrome']",,,397933,CN226082,,,,,,,,
mondo:0018349,MAN1B1-congenital disorder of glycosylation,"['congenital disorder of glycosylation type 2 due to MAN1B1 deficiency', 'congenital disorder of glycosylation type II due to MAN1B1 deficiency', 'carbohydrate deficient glycoprotein syndrome type II due to MAN1B1 deficiency', 'MAN1B1-congenital disorder of glycosylation', 'MAN1B1-CDG', 'intellectual disability-truncal obesity syndrome']",,,397941,C4518783,,,,,,,,
mondo:0018352,squamous cell carcinoma of penis,"['penile epidermoid cell carcinoma', 'penile epidermoid carcinoma', 'squamous cell carcinoma of penis', 'squamous cell carcinoma of the penis', 'PSCC', 'epidermoid carcinoma of penis', 'epidermoid carcinoma of the penis', 'epidermoid cell carcinoma of penis', 'epidermoid cell carcinoma of the penis', 'penile squamous car.(epidermoid)', 'penis squamous cell carcinoma', 'penile squamous cell carcinoma', 'penile squamous carcinoma (epidermoid)', 'penile squamous cell cancer']",5518,,398058,C0238348,,C7729,,,,,,
mondo:0018353,refractory celiac disease,"['refractory CD', 'refractory sprue', 'intractable celiac sprue', 'intractable coeliac sprue', 'type I refractory sprue', 'type II refractory sprue']",,,398063,CN226092,,,0009266,,,K90.0,,
mondo:0018354,Prader-Willi-like syndrome,['PWS-like'],,,398073,CN226094,,,,,,,,
mondo:0018355,SIM1-related Prader-Willi-like syndrome,"['Prader-Willi-like syndrome due to a point mutation', 'SIM1-related PWLS', 'PWS-like due to a point mutation', 'PWS-like due to point mutation']",,,398079,CN226095,,,,,,,,
mondo:0018356,secondary neonatal autoimmune disease,['Transplacentally acquired neonatal autoimmune disease'],,,398091,CN226097,,,,,,,,
mondo:0018357,neonatal antiphospholipid syndrome,"['neonatal antiphospholipid antibody syndrome', 'neonatal Hughes syndrome']",,,398097,CN226098,,,,,,,,
mondo:0018358,neonatal autoimmune hemolytic anemia,"['neonatal AIHA', 'neonatal AHA']",,,398109,,,,,,,,,
mondo:0018359,neonatal dermatomyositis,['neonatal DM'],,,398117,,,,,,,,,
mondo:0018360,neonatal lupus erythematosus,"['neonatal lupus', 'neonatal lupus syndrome', 'neonatal systemic lupus erythematosus', 'congenital lupus', 'congenital lupus erythematosus', 'neonatal SLE']",,,398124,C0409979,,C99236,0004537,C536397,,,,
mondo:0018361,neonatal scleroderma,,,,398127,,,,,,,,,
mondo:0018362,persistent idiopathic facial pain,"['PIFP', 'AFP', 'atypical facial pain']",,,398147,,,,,,,,,
mondo:0018363,focal facial dermal dysplasia,['FFDD'],,,398166,,"['0.509', '0.645', '-0.002453', '-0.329', '-0.1641', '0.005386', '0.2', '0.237', '-0.1234', '0.2444', '-0.2231', '-0.2478', '0.2343', '-0.04962', '-0.6436', '0.3547', '0.2406', '-0.675', '-0.1432', '-0.535', '-0.1699', '0.4575', '1.227', '0.24', '0.6587', '0.2507', '-0.3103', '-0.195', '0.537', '0.01634', '0.02644', '0.09814', '0.154', '0.3315', '0.501', '-0.3433', '-0.4463', '-0.02313', '-0.3828', '-0.8896', '-0.2695', '-0.3242', '-0.2057', '-0.1473', '0.2311', '-0.3381', '0.0787', '1.073', '-0.259', '-0.3936', '-0.1932', '-0.154', '0.2157', '-0.1327', '-0.2756', '-0.731', '0.2432', '-0.49', '-0.5444', '0.0786', '-0.07764', '0.1234', '-0.2299', '0.3267', '-0.4807', '-0.04053', '0.8765', '0.1693', '0.05966', '0.7803', '0.1724', '-0.11896', '0.1321', '-0.4143', '-0.1875', '0.2153', '0.0948', '-0.618', '-0.2245', '0.0795', '0.548', '0.2382', '0.1932', '0.4412', '-0.01347', '-0.5205', '-0.2869', '0.916', '0.563', '0.1925', '0.284', '0.4905', '0.5244', '0.3672', '0.964', '0.3467', '0.1383', '0.1906', '0.3315', '0.3472']",,,C537068,,,,
mondo:0018364,malignant epithelial tumor of ovary,"['epithelial cancer of ovary', 'malignant ovarian epithelial tumour', 'ovarian stromal cancer', 'ovarian malignant epithelial tumor', 'ovarian epithelial cancer', 'malignant ovarian surface epithelial-stromal neoplasm', 'ovarian malignant epithelial tumour', 'malignant ovarian surface epithelial-stromal tumour', 'ovarian epithelial tumor, malignant', 'malignant ovarian epithelial tumor', 'malignant ovarian surface epithelial-stromal tumor']",2151,,398934,,,C40026,,C538090,,,,
mondo:0018365,malignant non-epithelial tumor of ovary,"['ovarian malignant non-epithelial tumor', 'ovarian non-epithelial cancer', 'ovarian malignant non-epithelial tumour', 'non-epithelial cancer of ovary']",,,398940,CN205032,,,,,,,,
mondo:0018368,primary peritoneal serous/papillary carcinoma,"['primary peritoneal serous papillary carcinoma', 'primary peritoneal serous papillary adenocarcinoma', 'PPSPC', 'peritoneal serous papillary adenocarcinoma', 'primary serous papillary carcinoma of peritoneum']",6228,,398980,CN205035,,C7695,,,,,,
mondo:0018369,immature ovarian teratoma,"['immature teratoma of the ovary', 'malignant germ cell teratoma of the ovary', 'malignant teratoma of the ovary', 'ovary malignant teratoma', 'malignant germ cell teratoma of ovary', 'immature germ cell teratoma of ovary', 'ovarian immature germ cell teratoma', 'malignant ovarian teratoma', 'ovarian malignant teratoma', 'malignant ovarian germ cell teratoma', 'ovarian germ cell immature teratoma', 'immature teratoma', 'immature germ cell teratoma of the ovary', 'ovarian immature teratoma', 'malignant teratoma of ovary', 'immature teratoma of ovary', 'immature ovarian teratoma']",6331,,398987,CN205036,,C8111,,,,,,
mondo:0018370,KLHL9-related early-onset distal myopathy,,,,399081,,,,,,,,,
mondo:0018371,nebulin-related early-onset distal myopathy,['distal nebulin myopathy'],,,399103,,,,,,,,,
mondo:0018373,avascular necrosis,"['avascular necrosis of bone', 'AVN']",,,399164,,,C34841,,,,,,
mondo:0018374,secondary avascular necrosis,['secondary AVN'],,,399169,,,,,,,,,
mondo:0018375,traumatic avascular necrosis,['traumatic AVN'],,,399175,,,,,,,,,
mondo:0018376,secondary non-traumatic avascular necrosis,['secondary non-traumatic AVN'],,,399180,,,,,,,,,
mondo:0018378,osteonecrosis of the jaw,"['jaw osteonecrosis', 'ONJ', 'osteonecrosis of jaw']",,,399293,C2711248,,C63924,,,733.45,,,
mondo:0018379,primary avascular necrosis,['primary AVN'],,,399302,,,,,,,,,
mondo:0018380,idiopathic avascular necrosis,['idiopathic AVN'],,,399307,,,,,,,,,
mondo:0018381,osteochondrosis,"['epiphyseal necrosis', 'osteochondrosis not specified as adult or juvenile, of unspecified site', 'osteochondritis juvenilis', 'apophysitis', 'osteochondritis', 'epiphysitis']",8125,,399319,C0029429,,C34879,0008575,D055034,732.6,M42,,
mondo:0018382,epiphysiolysis of the hip,"['slipped upper femoral epiphysis', 'SufE', 'femoral head epiphysiolysis', 'epiphysiolysis of the upper femur', 'SCFE', 'slipped capital femoral epiphysis']",,,399329,,,,1001317,,,,,
mondo:0018383,osteonecrosis of genetic origin,"['genetic osteonecrosis', 'bone necrosis of genetic origin']",,,399380,,,,,,,,,
mondo:0018384,avascular necrosis of genetic origin,['genetic avascular necrosis'],,,399388,,,,,,,,,
mondo:0018385,osteochondrosis of genetic origin,['genetic osteochondrosis'],,,399391,,,,,,,,,
mondo:0018393,male infertility with azoospermia or oligozoospermia due to single gene mutation,,,,399805,CN225947,"['-0.517', '-0.534', '0.09906', '-0.6035', '-0.04715', '-0.315', '-0.0707', '0.503', '-0.4307', '-0.4192', '1.556', '-0.014755', '-0.2463', '1.085', '0.1047', '-0.1538', '0.039', '0.5327', '-0.4482', '-1.051', '-0.3438', '0.1719', '0.3474', '-0.2322', '0.4348', '-0.7144', '0.2', '-0.04788', '-0.588', '-0.4507', '0.6265', '-0.02328', '-0.3926', '-0.182', '0.177', '-0.03683', '-0.2664', '-0.07086', '0.2734', '-0.1726', '0.00884', '0.167', '0.0406', '-0.3083', '0.6807', '-0.669', '0.3254', '-0.7954', '0.7637', '0.522', '-0.6196', '-0.1273', '-0.1001', '0.674', '-0.1031', '0.6636', '0.4133', '0.1311', '-0.7505', '0.2568', '0.1465', '0.902', '0.01147', '0.02858', '-0.2494', '0.4312', '-0.03265', '0.4814', '-1.039', '0.577', '-0.3762', '0.2445', '0.00391', '-0.1841', '0.05832', '0.5195', '0.6978', '0.422', '-0.332', '0.2893', '-0.0571', '0.253', '0.1409', '-0.6836', '-0.01383', '-0.7075', '0.1627', '0.1932', '0.4348', '-0.5044', '-0.5327', '0.4011', '-0.6787', '1.053', '0.54', '-0.4001', '0.31', '-0.4639', '-0.636', '0.01443']",,,,,,,
mondo:0018394,male infertility with teratozoospermia due to single gene mutation,,,,399808,CN252642,"['-0.5303', '-0.5264', '0.1697', '-0.581', '-0.2632', '-0.3394', '0.1423', '0.654', '-0.5522', '-0.3665', '1.601', '-0.0635', '-0.234', '1.149', '-0.001904', '-0.2079', '0.1073', '0.526', '-0.5166', '-1.263', '-0.3206', '0.1091', '0.3271', '-0.2593', '0.3188', '-0.7344', '0.2366', '0.04602', '-0.7383', '-0.5054', '0.5835', '-0.0816', '-0.3506', '-0.2462', '0.01425', '0.08', '-0.2361', '-0.0054', '0.1365', '-0.09814', '0.1991', '0.1079', '0.197', '-0.2491', '0.884', '-0.7393', '0.4155', '-0.8174', '0.8076', '0.4106', '-0.8394', '-0.02559', '-0.003143', '0.731', '0.1613', '0.6035', '0.2246', '0.2524', '-0.74', '0.2118', '0.385', '1.049', '-0.1351', '0.1613', '-0.1692', '0.589', '-0.010994', '0.6235', '-1.192', '0.6675', '-0.3086', '0.314', '-0.02371', '-0.1638', '0.2391', '0.753', '0.5557', '0.4158', '-0.38', '0.369', '-0.07855', '0.3828', '0.08405', '-0.6533', '0.044', '-0.616', '0.1626', '0.006695', '0.3855', '-0.7373', '-0.503', '0.3196', '-0.7153', '1.157', '0.533', '-0.3257', '0.2563', '-0.2961', '-0.6733', '0.00504']",,,,,,,
mondo:0018408,cystic echinococcosis,"['Hydatidosis', 'liver echinococcus granulosus', 'echinococcus granulosus', 'unilocular hydatid disease', 'echinococcus granulosus infectious disease of liver', 'lung echinococcus granulosus', 'hydatid disease', 'Echinococcus granulosus infection of lung', 'unilocular echinococcosis', 'echinococcus granulosus infectious disease of thyroid', 'Echinococcus granulosus infection', 'Echinococcus granulosus infectious disease of liver', 'Echinococcus granulosus infection of thyroid', 'thyroid echinococcus granulosus']",1495,,400,C4303092,,,,,122.4,,10014096,
mondo:0018416,autosomal recessive spastic paraplegia type 59,['SPG59'],,,401795,CN226121,,,,,,,,
mondo:0018417,autosomal recessive spastic paraplegia type 60,['SPG60'],,,401800,CN226122,,,,,,,,
mondo:0018418,autosomal recessive spastic paraplegia type 66,['SPG66'],,,401815,CN226125,,,,,,,,
mondo:0018419,autosomal recessive spastic paraplegia type 67,['SPG67'],,,401820,CN226126,,,,,,,,
mondo:0018420,autosomal recessive spastic paraplegia type 68,['SPG68'],,,401825,CN226127,,,,,,,,
mondo:0018421,autosomal recessive spastic paraplegia type 69,['SPG69'],,,401830,CN226128,,,,,,,,
mondo:0018422,autosomal recessive spastic paraplegia type 70,['SPG70'],,,401835,CN226129,,,,,,,,
mondo:0018423,autosomal recessive spastic paraplegia type 71,['SPG71'],,,401840,CN226130,,,,,,,,
mondo:0018424,inherited lipoic acid biosynthesis defect,"['lipoic acid biosynthesis defect', 'rare inborn error of lipoate biosynthetic process', 'lipoic acid biosynthesis defects', 'inborn error of lipoate biosynthetic process', 'lipoate biosynthesis defect']",,,401854,,,,,,,,,
mondo:0018425,Huntington disease-like syndrome due to C9ORF72 expansions,"['Huntington disease phenocopy due to C9ORF72 expansions', 'C9ORF72-related Huntington disease-like syndrome', 'C9ORF72-related Huntington disease phenocopy']",,,401901,CN226138,,,,,,,,
mondo:0014844,premature ovarian failure 12,"['POF12', 'premature ovarian failure type 12', 'primary ovarian failure caused by mutation in SYCE1', 'premature ovarian failure 12', 'SYCE1 primary ovarian failure']",,616947,,C4310782,,,,,,,,
mondo:0014845,"spinocerebellar ataxia, autosomal recessive 22","['spinocerebellar ataxia, autosomal recessive type 22', 'VWA3B autosomal recessive cerebellar ataxia', 'autosomal recessive cerebellar ataxia caused by mutation in VWA3B', 'spinocerebellar ataxia, autosomal recessive 22', 'SCAR22']",0111614,616948,,C4310781,,,,,,,,
mondo:0014846,"spinocerebellar ataxia, autosomal recessive 23","['spinocerebellar ataxia, autosomal recessive 23', 'SCAR23', 'spinocerebellar ataxia, autosomal recessive type 23', 'autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to TUD deficiency', 'spinocerebellar ataxia autosomal recessive type 23']",0111613,616949,404493,C4310780,"['0.993', '0.1153', '-0.2261', '0.0413', '-0.312', '-0.4482', '0.6978', '0.2961', '-0.6216', '-0.4268', '0.0807', '-0.1169', '-0.5015', '0.4194', '0.00698', '0.0647', '-0.255', '-0.4607', '-0.612', '-0.625', '-0.269', '0.6895', '-0.0423', '-0.609', '-0.3154', '-0.1075', '-0.03125', '-0.1318', '-0.4277', '0.4248', '0.1244', '-0.5977', '0.2452', '0.02333', '0.7886', '0.4595', '-0.0646', '-0.02435', '-0.0703', '-0.49', '-0.1685', '-0.304', '0.003834', '-0.2421', '-0.5337', '-0.8857', '-0.1571', '0.2832', '0.683', '0.5703', '-0.1107', '0.1476', '-0.0719', '-0.3865', '-0.015236', '-0.2137', '-0.07184', '0.228', '-0.2113', '0.3687', '-0.706', '0.6787', '0.762', '-0.1307', '-0.333', '1.403', '0.2391', '0.003723', '-0.865', '0.6914', '0.933', '0.968', '0.0787', '-0.5186', '0.2162', '0.723', '0.9927', '0.503', '-0.3167', '0.3994', '-0.1208', '0.863', '0.4873', '0.3108', '0.4404', '0.0653', '0.155', '0.7383', '0.8496', '0.3125', '-0.056', '0.1087', '-0.2812', '0.2179', '0.11035', '0.332', '0.2778', '-0.5635', '0.3423', '0.3335']",,,,,,,
mondo:0014847,spermatogenic failure 15,"['SYCE1 azoospermia', 'azoospermia caused by mutation in SYCE1', 'spermatogenic failure type 15', 'spermatogenic failure 15', 'SPGF15']",0070172,616950,,C4310779,,,,,,,,
mondo:0014848,TELO2-related intellectual disability-neurodevelopmental disorder,"['YHFS', 'you-Hoover-Fong syndrome']",,616954,488642,C4310778,"['-0.2495', '0.02243', '0.4229', '-0.3005', '0.0699', '-0.2168', '0.1934', '0.5747', '-0.4504', '-0.04318', '-0.0809', '-0.2369', '-0.1741', '-0.1892', '-0.04327', '-0.012314', '0.1946', '0.04205', '-0.2125', '-0.5645', '0.2014', '0.2576', '0.1007', '-0.02745', '0.2462', '-0.0876', '-0.0835', '-0.013115', '0.1', '-0.1895', '0.1938', '-0.0953', '0.613', '0.271', '0.10974', '-0.11395', '-0.1599', '-0.2817', '-0.2428', '-0.2052', '0.2114', '-0.1736', '-0.1923', '0.08344', '0.1605', '-0.3015', '-0.05087', '0.2842', '-0.212', '0.336', '-0.2313', '0.2566', '0.05255', '-0.3262', '0.00968', '-0.11646', '-0.1587', '-0.0001422', '-0.04572', '-0.057', '0.2059', '-0.01366', '0.000985', '0.1741', '-0.4043', '-0.01131', '0.1881', '0.3486', '-0.326', '0.05014', '-0.4639', '0.3533', '-0.03842', '-0.1793', '0.1383', '-0.07025', '0.267', '0.1139', '-0.3242', '0.01087', '0.197', '0.02054', '-0.08124', '0.4746', '0.06903', '0.01412', '-0.0684', '0.333', '0.2644', '0.4448', '0.1008', '0.504', '0.005016', '0.0762', '0.3657', '0.147', '0.4224', '-0.2308', '0.5225', '0.4165']",,0009061,,,,,
mondo:0014850,retinitis pigmentosa and erythrocytic microcytosis,"['RPEM', 'retinitis pigmentosa and erythrocytic microcytosis']",,616959,,C4310776,"['-0.04904', '0.05682', '0.005196', '-0.01517', '0.01199', '-0.0718', '-0.012985', '0.04105', '-0.038', '-0.009056', '-0.02075', '-0.013435', '0.01084', '-0.01554', '-0.0395', '-0.05008', '-0.0135', '-0.01776', '-0.00695', '-0.10657', '-0.003487', '-0.02257', '0.02368', '-0.013535', '0.02614', '-0.00848', '-0.0237', '0.006718', '-0.02005', '-0.02943', '0.02979', '-0.01328', '0.0464', '0.02594', '0.01066', '-0.0426', '-0.01527', '-0.03226', '-0.02519', '-0.0635', '-0.004444', '-0.03357', '-0.004112', '-0.005753', '-0.00806', '-0.039', '-0.01186', '0.03732', '0.02063', '0.01582', '0.01181', '0.006996', '0.01178', '-0.01324', '0.00926', '-0.0364', '0.0846', '-0.02133', '-0.07367', '0.02737', '0.02367', '0.02417', '0.00078', '0.014404', '-0.01383', '-0.003794', '0.05737', '0.0686', '-0.0505', '0.05', '-0.0589', '-0.003384', '0.01224', '-0.0553', '0.02054', '0.01802', '0.0005765', '-0.01936', '0.01297', '-0.02411', '-0.0008926', '-0.01764', '-0.01578', '0.05414', '-0.00868', '0.00957', '0.01631', '0.04712', '0.04233', '0.02856', '0.011696', '0.03574', '0.01932', '0.0244', '0.09534', '0.02464', '0.0527', '-0.06152', '-0.01906', '0.009575']",,,,,,,
mondo:0014851,"hypercalcemia, infantile, 2","['hypercalcemia, infantile, 2', 'hypercalcemia, infantile, type 2', 'SLC34A1 autosomal recessive infantile hypercalcemia', 'HCINF2', 'autosomal recessive infantile hypercalcemia caused by mutation in SLC34A1']",,616963,,CN847585,,,,,,,,
mondo:0014853,autosomal dominant nonsyndromic hearing loss 70,"['DFNA70', 'autosomal dominant nonsyndromic deafness type 70', 'autosomal dominant nonsyndromic deafness 70', 'MCM2 autosomal dominant nonsyndromic deafness', 'deafness, autosomal dominant 70', 'autosomal dominant deafness 70', 'autosomal dominant nonsyndromic deafness caused by mutation in MCM2', 'deafness, autosomal dominant type 70']",0110592,616968,,C4310775,,,,,,,,
mondo:0014854,autosomal dominant nonsyndromic hearing loss 66,"['autosomal dominant deafness 66', 'autosomal dominant nonsyndromic deafness type 66', 'deafness, autosomal dominant type 66', 'DFNA66', 'autosomal dominant nonsyndromic deafness 66', 'CD164 autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness caused by mutation in CD164', 'deafness, autosomal dominant 66']",0110587,616969,,C4283893,,,,,,,,
mondo:0014855,"intellectual disability, autosomal dominant 42","['autosomal dominant non-syndromic intellectual disability caused by mutation in Gnb1', 'mental retardation, autosomal dominant 42', 'Gnb1 autosomal dominant non-syndromic intellectual disability', 'mental retardation, autosomal dominant type 42', 'autosomal dominant non-syndromic intellectual disability 42', 'intellectual disability, autosomal dominant type 42', 'GNB1 autosomal dominant non-syndromic intellectual disability', 'intellectual developmental disorder, autosomal dominant 42', 'autosomal dominant intellectual disability 42', 'MRD42', 'intellectual disability, autosomal dominant 42', 'autosomal dominant mental retardation 42']",0070072,616973,,C4310774,,,,,,,,
mondo:0014856,combined oxidative phosphorylation defect type 30,"['TRMT10C combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency caused by mutation in TRMT10C', 'combined oxidative phosphorylation deficiency 30', 'COXPD30', 'combined oxidative phosphorylation deficiency type 30']",0111471,616974,478042,C4310773,"['-0.4407', '0.1103', '-0.1279', '-0.0941', '-0.0194', '-0.569', '0.05115', '0.616', '-0.2844', '0.0687', '-0.3328', '-0.1993', '0.0479', '-0.08905', '0.09766', '-0.0529', '-0.02277', '-0.10455', '-0.5737', '-0.513', '0.2267', '-0.3706', '0.5107', '-0.00414', '0.087', '-0.03708', '0.254', '0.0805', '-0.2167', '-0.12036', '0.2632', '0.3013', '0.657', '0.11755', '-0.1318', '-0.3691', '-0.00813', '-0.2502', '0.06586', '-0.1787', '0.02414', '-0.2556', '0.01011', '0.3882', '-0.514', '-0.1456', '0.03262', '0.02824', '-0.1544', '0.1086', '-0.3335', '-0.1855', '0.1863', '-0.1072', '-0.1021', '-0.2224', '0.1521', '-0.014885', '0.01671', '0.2644', '0.1844', '0.12134', '0.3274', '-0.114', '-0.176', '0.1566', '0.1769', '0.3745', '-0.47', '0.183', '-0.1885', '0.10626', '0.007774', '0.001', '0.2144', '-0.1561', '0.09064', '-0.03967', '0.01746', '0.3997', '0.1182', '0.09314', '0.0696', '0.115', '-0.1037', '0.0361', '0.386', '0.3928', '0.5547', '0.008224', '0.3596', '0.00835', '-0.0647', '-0.0942', '0.5625', '0.5293', '0.3699', '-0.2966', '0.09235', '-0.0873']",,0009038,,,,,
mondo:0014857,"neurodevelopmental disorder with or without anomalies of the brain, eye, or heart","['NEDBEH', 'rere-related neurodevelopmental syndrome', 'neurodevelopmental disorder with or without anomalies of the brain, eye, or heart']",,616975,494344,C4310772,,,,,,,,
mondo:0014858,"intellectual disability, autosomal dominant 43","['HIVEP2 autosomal dominant non-syndromic intellectual disability', 'autosomal dominant intellectual disability 43', 'autosomal dominant mental retardation 43', 'autosomal dominant non-syndromic intellectual disability 43', 'intellectual disability, autosomal dominant type 43', 'mental retardation, autosomal dominant 43', 'autosomal dominant non-syndromic intellectual disability caused by mutation in HIVEP2', 'MRD43', 'autosomal dominant intellectual disability-43', 'HIVEP2-related intellectual disability', 'mental retardation, autosomal dominant type 43', 'intellectual disability, autosomal dominant 43']",0070073,616977,,C4310771,,,,,,,,
mondo:0014859,"developmental and epileptic encephalopathy, 37","['early infantile epileptic encephalopathy caused by mutation in FRRS1L', 'FRRS1L early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 37', 'epileptic encephalopathy, early infantile, type 37', 'EIEE37', 'DEE37', 'developmental and epileptic encephalopathy 37']",0080435,616981,,C4310770,,,,,,,,
mondo:0014860,polycystic liver disease 2,"['polycystic liver disease type 2', 'PCLD2', 'polycystic liver disease 2 with or without kidney cysts', 'polycystic liver disease 2']",,617004,,C4310769,,,,,,,,
mondo:0014861,"autoimmune disease, multisystem, infantile-onset, 2","['autoimmune disease, multisystem, infantile-onset caused by mutation in ZAP70', 'autoimmune disease, multisystem, infantile-onset, 2', 'autoimmune disease, multisystem, infantile-onset, type 2', 'ZAP70 autoimmune disease, multisystem, infantile-onset', 'ADMIO2']",,617006,,C4310768,,,,,,,,
mondo:0014862,"cerebral palsy, spastic quadriplegic, 3","['spastic quadriplegia caused by mutation in ADD3', 'cerebral palsy, spastic quadriplegic, 3', 'ADD3 spastic quadriplegia', 'cerebral palsy, spastic quadriplegic, type 3', 'CPSQ3']",0081361,617008,,C4310767,,,,,,,,
mondo:0014863,"macrocephaly, dysmorphic facies, and psychomotor retardation","['macrocephaly, dysmorphic facies, and psychomotor retardation', 'MDFPMR']",,617011,,C4310766,"['-0.02812', '0.04025', '0.02623', '-0.03976', '0.01197', '-0.05103', '-0.004906', '0.07837', '-0.05063', '-0.01784', '-0.01447', '-0.00375', '-0.0009265', '-0.003323', '-0.03616', '-0.007435', '0.01432', '-0.03108', '-0.03842', '-0.0836', '0.013985', '-0.00831', '0.04645', '-0.02707', '0.01924', '-0.008896', '-0.01077', '-0.004875', '-0.007023', '-0.01816', '0.0544', '-0.00875', '0.06635', '0.01164', '0.013214', '-0.01298', '-0.02615', '-0.013435', '-0.00207', '-0.05222', '0.0157', '-0.04492', '0.012535', '-0.01109', '-0.003187', '-0.04666', '-0.002949', '0.0303', '-0.00665', '0.01097', '-0.02962', '0.0009437', '0.004906', '-0.007236', '-0.02164', '-0.02293', '0.01102', '-0.02374', '-0.04636', '0.02263', '0.00504', '0.01895', '-0.00433', '0.00844', '0.00455', '0.003878', '0.0325', '0.0461', '-0.05746', '0.05548', '-0.03635', '0.02417', '0.03348', '-0.02377', '-0.00295', '0.03436', '0.02122', '-0.011795', '-0.04083', '-0.02052', '0.005993', '8.41e-05', '-0.02971', '0.04486', '-0.001911', '0.01476', '0.002747', '0.0422', '0.0651', '0.009186', '0.011246', '0.04385', '-0.005608', '0.01883', '0.0778', '0.02245', '0.03012', '-0.04074', '0.03906', '0.01636']",,,,,,,
mondo:0014864,hypermanganesemia with dystonia 2,"['SLC39A14 hypermanganesemia with dystonia', 'hypermanganesemia with dystonia caused by mutation in SLC39A14', 'hypermanganesemia with dystonia type 2', 'HMNDYT2', 'hypermanganesemia with dystonia 2']",0080537,617013,521406,C4310765,,,,,,,,
mondo:0014865,autosomal recessive severe congenital neutropenia due to CSF3R deficiency,"['neutropenia, Severe congenital, 7, autosomal recessive', 'SCN7', 'neutropenia, severe congenital, 7, autosomal recessive']",0112129,617014,420702,C4310764,,,,,,,,
mondo:0014866,Charcot-Marie-Tooth disease axonal type 2T,"['CMT2T', 'Charcot-Marie-Tooth disease, axonal, type 2T', 'DNAJB2-related CMT2', 'autosomal recessive axonal Charcot-Marie-Tooth disease type 2T', 'AR-CMT2T', 'DNAJB2-related Charcot-Marie-Tooth disease type 2', 'Charcot-Marie-Tooth neuropathy, type 2T', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2T', 'Charcot-Marie-Tooth neuropathy type 2T']",0110160,617017,443950,C4015635,,,,,,,,
mondo:0014867,spinocerebellar ataxia 43,"['autosomal dominant cerebellar ataxia caused by mutation in MME', 'spinocerebellar ataxia 43', 'spinocerebellar ataxia type 43', 'MME autosomal dominant cerebellar ataxia', 'SCA43']",0111745,617018,497764,C4310763,"['-0.07025', '-0.3833', '0.02379', '0.1583', '-0.2744', '-1.008', '0.1475', '0.0513', '-0.733', '-0.8467', '0.3303', '0.2676', '-0.2952', '0.2668', '0.3804', '-0.4985', '-0.1681', '-0.3005', '0.003336', '-1.067', '-0.1841', '-0.3384', '0.106', '-0.5366', '0.6226', '-0.4094', '-0.2893', '0.2542', '-0.1627', '-0.699', '0.05304', '0.4646', '-0.506', '-0.2228', '0.2566', '0.233', '-0.1978', '0.08777', '0.4807', '0.2778', '0.3472', '0.19', '-0.512', '0.514', '0.532', '-0.4648', '0.2183', '0.5586', '0.378', '-0.06757', '-0.18', '0.1737', '-0.0835', '-0.4116', '-0.00759', '-0.8193', '0.4219', '0.4639', '-0.2076', '0.385', '-0.5425', '0.3342', '0.2578', '-0.2004', '-0.4868', '0.715', '0.3984', '0.586', '-0.6836', '0.4395', '0.86', '0.5234', '-0.1571', '-0.725', '0.8345', '0.1902', '0.1876', '0.3894', '0.2695', '0.4138', '-0.4612', '-0.7866', '0.3936', '0.782', '-0.229', '-0.616', '0.1915', '-0.11115', '0.52', '0.5356', '0.331', '0.43', '0.2119', '0.01578', '0.962', '1.196', '0.419', '0.4934', '-0.426', '0.0699']",,0009060,,,,,
mondo:0014868,"developmental and epileptic encephalopathy, 38","['early infantile epileptic encephalopathy caused by mutation in ARV1', 'DEE38', 'epileptic encephalopathy, early infantile, type 38', 'EIEE38', 'developmental and epileptic encephalopathy 38', 'ARV1 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 38']",0080417,617020,,C4310762,,,,,,,,
mondo:0014869,hydrops-lactic acidosis-sideroblastic anemia-multisystemic failure syndrome,"['hydrops, lactic acidosis, and sideroblastic anemia', 'hydrops, lactic acidosis, and sideroblastic anaemia', 'HLASA']",,617021,528091,C4310761,,,,,,,,
mondo:0014870,NEK9-related lethal skeletal dysplasia,"['lethal congenital contracture syndrome 10', 'lethal congenital contracture syndrome type 10', 'LCCS10', 'lethal skeletal dysplasia-fetal akinesia-contractures-thoracic dysplasia-pulmonary hypoplasia syndrome']",,617022,464366,C4310760,,,,,,,,
mondo:0014871,retinitis pigmentosa 75,"['retinitis pigmentosa 75', 'RP75', 'AGBL5 retinitis pigmentosa', 'retinitis pigmentosa type 75', 'retinitis pigmentosa caused by mutation in AGBL5']",0110361,617023,,C4310759,,,,,,H35.5,,
mondo:0014872,congenital stationary night blindness 1H,"['GNB3 congenital stationary night blindness', 'congenital stationary night blindness type 1H', 'night blindness, congenital stationary, type 1H', 'CSNB1H', 'congenital stationary night blindness caused by mutation in GNB3']",0110866,617024,,C4310758,,,,,,,,
mondo:0014873,nevus comedonicus syndrome,"['Nevus comedonicus', 'NC', 'nevus comedonicus, somatic', 'comedo Nevus', 'acneiform Nevus', 'NEVUS comedonicus', 'acne Nevus', 'pilosebaceous nevoid disorder']",,617025,64754,C0265987,"['-0.3137', '-0.0502', '0.2527', '-0.4646', '0.3599', '-0.01602', '-0.01266', '0.192', '-0.7705', '-0.1848', '-0.2059', '0.247', '-0.006714', '-0.01616', '-0.3958', '0.3665', '0.3533', '-0.4812', '-0.01124', '-0.746', '-0.04767', '0.04794', '0.2437', '-0.10016', '-0.1131', '-0.0832', '0.1005', '0.2351', '-0.10815', '-0.11383', '0.4917', '-0.2874', '0.2428', '0.01741', '0.1316', '0.3054', '-0.1664', '-0.1578', '-0.2074', '-0.1013', '0.2362', '-0.0328', '0.1876', '0.0485', '-0.0825', '-0.12256', '-0.09436', '0.3254', '-0.03845', '0.1353', '-0.0857', '0.287', '0.1853', '0.0692', '-0.5977', '0.1059', '-0.007423', '0.0199', '-0.554', '-0.06494', '-0.05676', '-0.09674', '-0.3345', '0.2341', '-0.2406', '0.1906', '0.567', '0.601', '-0.1626', '0.25', '-0.2476', '0.2737', '0.0911', '0.1714', '-0.1508', '-0.03836', '0.1407', '0.1056', '-0.1685', '-0.603', '-0.1298', '0.112', '0.3452', '0.2098', '0.06003', '-0.3953', '-0.2455', '0.1312', '0.02716', '0.3203', '0.10693', '0.4724', '0.3035', '0.0925', '0.558', '-0.1637', '0.1241', '-0.0896', '0.496', '0.1426']",C3946,,,,,,
mondo:0014874,"pontocerebellar hypoplasia, type 2F","['non-syndromic pontocerebellar hypoplasia caused by mutation in TSEN15', 'TSEN15 non-syndromic pontocerebellar hypoplasia', 'pontocerebellar hypoplasia, type 2F', 'PCH2F']",0112329,617026,,C4310757,,,,,,,,
mondo:0014875,"hyperaldosteronism, familial, type IV","['FH 4', 'hyperaldosteronism, familial, type 4', 'hyperaldosteronism, familial, type IV', 'HALD4', 'aldosteronism, primary, and hypertension', 'familial hyperaldosteronism type IV']",,617027,642671,C4310756,,,,,,,,
mondo:0014876,"intellectual disability, autosomal recessive 54","['autosomal recessive non-syndromic intellectual disability caused by mutation in TNIK', 'MRT54', 'mental retardation, autosomal recessive 54', 'intellectual disability, autosomal recessive type 54', 'TNIK autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive type 54', 'intellectual developmental disorder 54', 'intellectual disability, autosomal recessive 54']",0081216,617028,,C4310755,,,,,,,,
mondo:0014877,"myopathy, distal, 5","['adenylosuccinate synthetase-like 1-related distal myopathy', 'myopathy, distal, type 5', 'distal myopathy caused by mutation in ADSSL1', 'ADSSL1 distal myopathy', 'ADSSL1-related distal myopathy', 'MPD5']",,617030,482601,C4310754,,,,,,,,
mondo:0014878,patent ductus arteriosus 2,"['patent ductus arteriosus type 2', 'PDA2', 'patent ductus arteriosus 2']",,617035,,C4284595,,,,,,,,
mondo:0014880,Duane retraction syndrome 3 with or without deafness,"['MAFB Duane retraction syndrome', 'Duane syndrome type 3', 'Duane retraction syndrome 3 with or without deafness', 'DURS3', 'Duane retraction syndrome 3', 'Duane retraction syndrome caused by mutation in MAFB']",,617041,,C4310752,,,,,,,,
mondo:0014881,transketolase deficiency,"['TKT deficiency', 'short stature, developmental delay, and congenital heart defects', 'SDDHD', 'short stature-developmental delay-congenital heart defect syndrome']",,617044,488618,C4310751,,,,,,,,
mondo:0014882,hereditary spastic paraplegia 77,"['hereditary spastic paraplegia type 77', 'autosomal recessive spastic paraplegia type 77', 'FARS2 hereditary spastic paraplegia', 'spastic paraplegia 77, autosomal recessive', 'autosomal recessive spastic paraplegia 77', 'hereditary spastic paraplegia caused by mutation in FARS2', 'SPG77']",0110822,617046,466722,C4310750,,,,,,,,
mondo:0014883,hypertrophic cardiomyopathy 26,"['hypertrophic cardiomyopathy type 26', 'cardiomyopathy, familial restrictive, 5', 'cardiomyopathy, familial restrictive 5', 'hypertrophic cardiomyopathy caused by mutation in FLNC', 'CMH26', 'FLNC hypertrophic cardiomyopathy', 'cardiomyopathy, familial hypertrophic, 26', 'cardiomyopathy, familial hypertrophic, type 26', 'cardiomyopathy familial hypertrophic 26']",0110327,617047,,C4310749,,,,,,,,
mondo:0014884,"cholestasis, progressive familial intrahepatic, 5","['NR1H4 progressive familial intrahepatic cholestasis', 'NR1H4 deficiency', 'cholestasis, progressive familial intrahepatic, type 5', 'PFIC5', 'cholestasis, progressive familial intrahepatic, 5', 'progressive familial intrahepatic cholestasis caused by mutation in NR1H4']",0070225,617049,480476,CN776839,,,,,,,,
mondo:0014885,Hermansky-Pudlak syndrome 10,"['Hermansky-Pudlak syndrome 10', 'Hermansky-Pudlak syndrome type 10', 'AP3D1 Hermansky-Pudlak syndrome', 'Hermansky-Pudlak syndrome caused by mutation in AP3D1', 'HPS10']",,617050,,C4310746,,,,,,,,
mondo:0014886,severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome,"['MRT55', 'intellectual disability, autosomal recessive type 55', 'mental retardation, autosomal recessive 55', 'neurodevelopmental disorder with microcephaly and gray sclerae', 'neurodevelopmental disorder with microcephaly and grey sclerae', 'mental retardation, autosomal recessive type 55', 'intellectual disability, autosomal recessive 55']",,617051,488627,C4310745,,,,,,,,
mondo:0014887,bone marrow failure syndrome 3,"['BMFS3', 'bone marrow failure syndrome type 3', 'bone marrow failure syndrome 3', 'bone marrow failure syndrome caused by mutation in DNAJC21', 'DNAJC21 bone marrow failure syndrome']",,617052,,C4310744,,,,,,,,
mondo:0014888,MIRAGE syndrome,"['myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital anomalies-enteropathy syndrome', 'myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital phenotypes-enteropathy syndrome', 'mirage syndrome', 'mirage', 'myelodysplasia, infection, restriction of Growth, adrenal Hypoplasia, genital phenotypes, and enteropathy']",,617053,494433,C4284088,"['-0.01161', '0.01456', '-0.0015135', '0.003275', '0.005806', '-0.03017', '0.00939', '0.01886', '-0.03108', '-0.01653', '0.001712', '0.0011215', '-0.006603', '0.01036', '-0.00756', '-0.01086', '-0.000152', '0.00446', '-0.011826', '-0.03717', '-0.004276', '-0.01967', '0.01245', '-0.004036', '0.001403', '0.001381', '-0.01921', '-0.010475', '0.01443', '-0.008125', '0.01576', '-0.000764', '0.02655', '0.006443', '-0.003883', '-0.01814', '0.0061', '-0.01001', '0.00797', '-0.03647', '0.003502', '-0.01656', '0.00328', '-0.0208', '0.012566', '-0.01561', '-0.007214', '0.01065', '0.002275', '0.004883', '-0.00554', '0.0001642', '0.01287', '0.003456', '-0.00945', '-0.00377', '0.01756', '0.002888', '-0.02286', '-0.004047', '0.00856', '0.007324', '-0.003609', '-0.00474', '0.007736', '-0.004288', '0.01772', '0.02257', '-0.01826', '0.011284', '-0.01266', '0.00459', '0.00824', '-0.00939', '-0.000754', '0.009766', '0.008484', '0.002668', '-0.01442', '-0.010796', '0.004852', '0.0002234', '-0.00494', '0.03372', '0.0001882', '0.00425', '0.001743', '0.01958', '0.02429', '0.006313', '0.013405', '0.02457', '0.001319', '0.00989', '0.03516', '0.005207', '0.0298', '-0.02682', '-0.01289', '0.00447']",C147530,,,,,,
mondo:0014889,"striatonigral degeneration, childhood-onset","['striatonigral Degeneration, childhood-onset', 'childhood-onset basal ganglia degeneration syndrome', 'Lenk-Ploski syndrome', 'SNDC']",,617054,497906,C4310743,"['-0.03424', '0.0319', '0.02316', '-0.02904', '-0.0018835', '-0.10486', '0.03494', '0.1', '-0.04602', '-0.04843', '-0.04617', '0.02133', '-0.04425', '0.02248', '-0.005783', '-0.0354', '-0.00762', '-0.0226', '-0.0197', '-0.1412', '0.00892', '-0.00435', '0.02734', '0.005116', '0.01441', '-0.0002837', '-0.01047', '-0.02374', '-0.03995', '-0.02226', '0.05228', '-0.0275', '0.05637', '0.03583', '0.03677', '-0.001744', '-0.0213', '-0.000985', '-0.0202', '-0.05655', '0.00337', '-0.08484', '-0.008766', '-0.004112', '-0.00093', '-0.04495', '0.001148', '0.04034', '0.008316', '-0.00536', '0.01796', '0.00838', '-0.00322', '-0.0482', '-0.01539', '-0.03613', '0.02707', '-0.03038', '-0.0633', '0.01395', '0.02469', '0.02415', '0.01231', '0.01083', '-0.00946', '0.01855', '0.06064', '0.06604', '-0.04028', '0.05362', '-0.04184', '0.01352', '0.00699', '-0.02153', '0.03662', '0.03568', '0.003103', '0.01017', '-0.03592', '0.005405', '0.0085', '-0.0002201', '-0.014046', '0.0961', '-0.013794', '-0.006866', '0.02655', '0.026', '0.0763', '-0.001643', '0.0364', '0.07874', '-0.0325', '0.04404', '0.10223', '0.04077', '0.07385', '-0.05466', '-0.01464', '0.0181']",,,,,,,
mondo:0014890,PERCHING syndrome,"['Postural and Palatal abnormalities; Exophthalmos and Enteral-tube dependency/feeding issues; Respiratory distress and Retinitis pigmentosa; Contractures and Camptodactyly; Hypertelorism and Hirsutism; Intrauterine growth retardation (IUGR)/growth failure and Intellectual disability/developmental delay; Nevus flammeus and Neurologic malformations;and facial Gestalt/grimacing and Genitourinary abnormalities', 'cold-induced sweating syndrome 3', 'Crisponi/cold-induced sweating syndrome 3', 'cold-induced sweating syndrome type 3', 'cold-induced sweating syndrome caused by mutation in KLHL7', 'CRISPONI/cold-induced sweating syndrome 3', 'PERCHING', 'CISS3', 'KLHL7-related bohring-opitz-like/cold-induced sweating-like overlap syndrome', 'KLHL7 cold-induced sweating syndrome']",0080331,617055,603684,C4310742,,,,,,,,
mondo:0014891,"hyperuricemic nephropathy, familial juvenile type 4","['HNFJ4', 'hyperuricemic NEPHROPATHY, familial juvenile, 4', 'SEC61A1-related autosomal dominant tubulointerstitial kidney disease', 'familial juvenile hyperuricemic nephropathy caused by mutation in SEC61A1', 'ADTKD-SEC61A1', 'tubulointerstitial kidney disease, autosomal dominant, 5', 'hyperuricemic nephropathy, familial juvenile, type 4', 'SEC61A1 familial juvenile hyperuricemic nephropathy', 'hyperuricemic nephropathy, familial juvenile, 4']",,617056,,C4310741,,,,,,,,
mondo:0014892,micrognathia-recurrent infections-behavioral abnormalities-mild intellectual disability syndrome,"['mercer-Ba syndrome', 'mental retardation, autosomal dominant 44', 'autosomal dominant mental retardation 44', 'autosomal dominant non-syndromic intellectual disability 44', 'intellectual disability, autosomal dominant 44', 'intellectual developmental disorder, autosomal dominant 44, with microcephaly', 'MEBAS', 'autosomal dominant intellectual disability 44', 'MRD44']",0070074,617061,476126,C4310740,,,,,,,,
mondo:0014893,Okur-Chung neurodevelopmental syndrome,"['OCNDS', 'Okur-Chung neurodevelopmental syndrome']",,617062,,C4310739,"['-0.02292', '0.05438', '0.01319', '-0.01863', '0.02594', '-0.06137', '-0.004208', '0.0574', '-0.04355', '-0.03864', '-0.013084', '-0.01825', '0.00959', '0.003843', '-0.010284', '-0.0285', '-0.00643', '-0.00765', '-0.02742', '-0.0918', '0.002964', '-0.01611', '0.04282', '-0.0321', '0.0273', '-0.03207', '-0.001471', '-0.002937', '0.03143', '-0.04672', '0.04263', '-0.005383', '0.05405', '0.02118', '0.00558', '-0.02528', '0.005695', '-0.02077', '-0.0142', '-0.06573', '0.02965', '-0.05676', '0.009415', '-0.02081', '-0.00010985', '-0.0634', '-0.02766', '0.0334', '0.003849', '0.00942', '-0.02997', '-0.001301', '-0.01016', '-0.002148', '-0.02196', '-0.00858', '0.04208', '-0.02116', '-0.05035', '0.01518', '0.04166', '0.01315', '0.015175', '0.02177', '0.004143', '0.005238', '0.05832', '0.01642', '-0.05142', '0.068', '-0.07367', '0.0191', '0.00793', '-0.01336', '0.0111', '0.01044', '0.00879', '-0.004604', '-0.0535', '-0.02122', '0.02055', '0.02403', '-0.0337', '0.0833', '0.001827', '0.01894', '0.01119', '0.04474', '0.05994', '0.03041', '0.0307', '0.05734', '-0.001921', '0.01631', '0.0849', '0.010506', '0.05655', '-0.0734', '-0.01154', '0.01114']",,,,,,,
mondo:0014894,Meier-Gorlin syndrome 7,"['CDC45 Meier-Gorlin syndrome', 'Meier-Gorlin syndrome type 7', 'MGORS7', 'Meier-Gorlin syndrome caused by mutation in CDC45', 'Meier-Gorlin syndrome 7']",0080518,617063,,C4310738,,,,,,,,
mondo:0014895,"developmental and epileptic encephalopathy, 40","['early infantile epileptic encephalopathy caused by mutation in GUF1', 'DEE40', 'EIEE40', 'GUF1 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 40', 'epileptic encephalopathy, early infantile, type 40', 'developmental and epileptic encephalopathy 40']",0080427,617065,,C4310737,,,,,,,,
mondo:0014896,congenital muscular dystrophy-respiratory failure-skin abnormalities-joint hyperlaxity syndrome,"['congenital muscular dystrophy, Davignon-Chauveau type', 'MDCDC', 'muscular dystrophy, congenital, Davignon-Chauveau type']",,617066,486815,C4310736,,,,,,,,
mondo:0014898,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3","['PEOB3', 'progressive external ophthalmoplegia, autosomal recessive 3', 'TK2 autosomal recessive progressive external ophthalmoplegia', 'autosomal recessive progressive external ophthalmoplegia caused by mutation in TK2', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 3', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 3']",0111523,617069,,C4310734,,,,,,,,
mondo:0014899,adult-onset multiple mitochondrial DNA deletion syndrome due to DGUOK deficiency,"['progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 4', 'adult-onset multiple mtDNA deletion syndrome due to DGUOK deficiency', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 4', 'progressive external ophthalmoplegia, autosomal recessive 4', 'PEOB4']",0111516,617070,329314,C4310733,"['-1.157', '0.3228', '0.1361', '-0.504', '-0.389', '-0.6074', '0.2656', '0.8306', '-0.59', '0.1643', '0.2478', '0.0478', '0.1237', '-0.3672', '0.3032', '-0.2117', '-0.1259', '0.1149', '-0.546', '-0.741', '0.545', '-0.4263', '-0.0823', '0.04623', '0.1613', '0.3564', '-0.0702', '-0.06946', '-0.3801', '-0.2556', '0.2351', '0.588', '0.6587', '0.10034', '-0.1998', '-0.8574', '-0.502', '-0.0583', '-0.6973', '-0.1953', '0.1456', '-0.581', '-0.1334', '0.444', '0.1409', '-0.588', '-0.02592', '-0.07477', '0.002493', '-0.253', '-0.5405', '0.4238', '-0.4456', '0.03882', '-0.2822', '-0.4202', '0.5894', '-0.6353', '-0.3516', '-0.2837', '0.3928', '0.02419', '0.3188', '0.3352', '-0.547', '0.3877', '0.3357', '0.508', '-0.03632', '0.2488', '-0.515', '-0.1012', '0.0667', '0.1721', '0.521', '-0.1405', '0.3662', '0.2325', '0.06464', '-0.2092', '0.3628', '0.3098', '0.0883', '0.776', '0.09485', '0.3555', '0.1996', '0.538', '0.4907', '-0.0615', '0.6675', '0.5405', '0.2244', '-0.53', '0.7715', '0.714', '0.269', '0.3135', '-0.1555', '0.0994']",,,,,,,
mondo:0014900,autosomal recessive limb-girdle muscular dystrophy type 2Y,"['TOR1AIP1 autosomal recessive limb-girdle muscular dystrophy', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in TOR1AIP1', 'muscular dystrophy, limb-girdle, type 2Y', 'autosomal recessive muscular dystrophy due to LAP1B deficiency', 'LGMD2Y', 'muscular dystrophy, autosomal recessive, with rigid spine and distal joint contractures', 'autosomal recessive muscular dystrophy due to Torsin-1A-interacting protein 1 deficiency', 'muscular dystrophy with progressive weakness, distal contractures and rigid spine', 'muscular dystrophy, limb-girdle, type 2y']",0110289,617072,424261,C4310731,,C181000,,,,,,
mondo:0014901,"tooth agenesis, selective, 8","['tooth agenesis, selective, 8', 'WNT10B tooth agenesis', 'STHAG8', 'tooth agenesis caused by mutation in WNT10B', 'tooth agenesis, selective, type 8']",,617073,,C4310730,,,,,,,,
mondo:0014902,"nasopharyngeal carcinoma, susceptibility to, 3","['nasopharyngeal carcinoma, susceptibility to, type 3', 'nasopharyngeal carcinoma caused by mutation in MST1R', 'MST1R nasopharyngeal carcinoma', 'nasopharyngeal carcinoma, susceptibility to, 3', 'NPCA3', 'susceptibility to nasopharyngeal carcinoma 3']",,617075,,,,,,,,,,
mondo:0014903,"seizures, benign familial infantile, 5","['seizures, benign familial infantile, 5', 'seizures, benign familial infantile, type 5', 'benign familial infantile epilepsy caused by mutation in SCN8A', 'SCN8A benign familial infantile epilepsy', 'convulsions, benign familial infantile, 5', 'BFIS5']",0081118,617080,,C4310728,,,,,,,,
mondo:0014904,"congenital disorder of glycosylation, type IAA","['CDG1AA', 'congenital disorder of glycosylation, type 1aa', 'congenital disorder of glycosylation, type IAA']",0080553,617082,,C4310727,,,,,,,,
mondo:0014905,encephalopathy due to defective mitochondrial and peroxisomal fission 2,"['encephalopathy due to defective mitochondrial and peroxisomal fission type 2', 'EMPF2', 'MFF-associated encephalopathy due to peroxisomal and mitochondrial fission defect', 'Leigh-like basal ganglia disease-optic atrophy-peripheral neuropathy syndrome', 'encephalopathy due to defective mitochondrial and peroxisomal fission 2']",,617086,485421,C4310726,,,,,,,,
mondo:0014906,"Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2a2b;","['CMT2A2B', 'Charcot-Marie-Tooth disease type 2A2B', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2A2B', 'Charcot-Marie-Tooth disease, axonal, type 2A2B']",0111557,617087,,C4310725,,C150647,,,,,,
mondo:0014907,short-rib thoracic dysplasia 15 with polydactyly,"['SRTD15', 'short-rib thoracic dysplasia 15 with polydactyly']",,617088,,C4310724,,,,,,,,
mondo:0014908,"microcephaly 17, primary, autosomal recessive","['autosomal recessive primary microcephaly caused by mutation in cit', 'cit autosomal recessive primary microcephaly', 'CIT autosomal recessive primary microcephaly', 'MCPH17', 'microcephaly 17, primary, autosomal recessive']",0070288,617090,,C4310723,,,,,,,,
mondo:0014909,primary ciliary dyskinesia 34,"['ciliary dyskinesia, primary, type 34', 'ciliary dyskinesia, primary, 34, without situs inversus', 'CILD34', 'primary ciliary dyskinesia caused by mutation in DNAJB13', 'primary ciliary dyskinesia type 34', 'primary ciliary dyskinesia 34 without situs inversus', 'ciliary dyskinesia, primary, 34', 'DNAJB13 primary ciliary dyskinesia']",0110610,617091,,C4310722,,,,,,,,
mondo:0014910,primary ciliary dyskinesia 35,"['ciliary dyskinesia, primary, type 35', 'primary ciliary dyskinesia type 35', 'CILD35', 'ciliary dyskinesia, primary, 35', 'ciliary dyskinesia, primary, 35, with or without situs inversus', 'primary ciliary dyskinesia caused by mutation in TTC25', 'primary ciliary dyskinesia 35 with or without situs inversus', 'TTC25 primary ciliary dyskinesia']",0110620,617092,,C4310721,,,,,,,,
mondo:0014911,"growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy","['Growth retardation, intellectual developmental disorder, hypotonia, and hepatopathy', 'GRIDHH', 'growth retardation, impaired intellectual development, hypotonia, and hepatopathy']",,617093,541423,C4310720,"['-0.265', '0.10364', '0.4773', '-0.4958', '0.324', '-0.4778', '0.2338', '0.4146', '-0.1438', '0.1262', '-0.2896', '-0.06793', '-0.1744', '-0.04318', '-0.351', '-0.2812', '0.3928', '0.03943', '-0.3499', '-0.6455', '0.1619', '-0.403', '0.06384', '-0.0189', '-0.01575', '0.01938', '0.0759', '-0.10333', '0.09375', '-0.3606', '0.08417', '-0.01054', '0.4429', '0.418', '-0.1603', '-0.1053', '-0.3398', '-0.2603', '-0.3062', '0.002703', '-0.2374', '-0.0548', '0.1691', '0.3953', '-0.3528', '-0.3054', '0.1559', '0.01761', '-0.3066', '-0.02254', '-0.515', '0.1316', '0.3599', '0.072', '-0.06854', '0.04727', '-0.013145', '-0.3376', '-0.3103', '0.01753', '0.2102', '-0.0188', '-0.05734', '-0.2063', '0.1128', '-0.1497', '0.2203', '0.539', '-0.3162', '0.10504', '-0.4546', '0.04425', '0.06537', '-0.2598', '-0.05472', '-0.2448', '0.4536', '-0.21', '-0.01912', '0.1532', '-0.07605', '0.05133', '-0.4949', '0.2401', '-0.04752', '0.3538', '0.1882', '0.3237', '0.3274', '0.4412', '0.609', '0.477', '-0.2156', '0.05737', '0.3357', '0.3035', '0.2056', '-0.336', '0.4148', '0.2876']",,0009155,,,,,
mondo:0014912,infantile-onset periodic fever-panniculitis-dermatosis syndrome,"['otulin-related autoinflammatory syndrome', 'otulipenia', 'autoinflammation, panniculitis and dermatosis syndrome', 'Autoinflammation, panniculitis, and dermatosis syndrome', 'AUTOINFLAMMATION, panniculitis, and dermatosis syndrome', 'AIPDS', 'ORAS', 'otulin deficiency']",0080163,617099,500062,C4310614,,,,,,,,
mondo:0014914,Dias-Logan syndrome,"['intellectual developmental disorder with persistence of foetal HEMOGLOBIN', 'intellectual developmental disorder with persistence of fetal Hemoglobin', 'intellectual developmental disorder with hereditary persistence of fetal Hemoglobin', 'DILOS', 'intellectual developmental disorder with hereditary persistence of foetal Haemoglobin', 'intellectual developmental disorder with persistence of fetal HEMOGLOBIN', 'Dias-Logan syndrome', 'BCL11A-related intellectual developmental disorder with persistence of fetal hemoglobin', 'BCL11A-related intellectual developmental disorder with persistence of foetal haemoglobin', 'BCL11A-related BAFopathy', 'intellectual developmental disorder with persistence of foetal Haemoglobin']",,617101,,C4310833,"['-0.005398', '-0.000114', '-0.0029', '0.002407', '-0.006836', '-0.00828', '-0.006443', '0.00183', '-0.01081', '0.0002916', '0.000834', '-0.00642', '0.00628', '-0.00545', '0.00653', '-0.002264', '-0.01133', '-0.004974', '-0.008995', '-0.01444', '-0.000308', '0.000531', '0.013504', '-0.0033', '-0.001634', '0.003405', '0.00395', '-0.001507', '0.005493', '-0.00851', '0.007275', '-0.0003047', '0.005478', '0.001684', '-0.003128', '-0.0005045', '-0.011375', '-0.0004053', '-0.008804', '-0.005104', '0.000419', '-0.01761', '0.01205', '-0.008385', '0.0053', '-0.01765', '-0.0009418', '0.01379', '-0.002302', '0.00879', '-0.00786', '0.0089', '0.002037', '0.002087', '-0.008064', '0.001259', '0.0007806', '-0.001742', '-0.014824', '0.00963', '0.003824', '-0.005836', '0.004223', '0.005745', '0.006027', '0.003292', '0.00548', '-0.003775', '-0.01633', '0.02007', '-0.01182', '0.004505', '-0.007168', '-0.0003488', '0.01099', '0.005707', '6.914e-05', '-0.0103', '-0.005123', '-0.002378', '-0.003319', '0.004642', '-0.00204', '0.01764', '0.00777', '-0.010506', '0.00823', '0.01563', '0.012146', '-0.002234', '-0.002068', '0.014915', '-0.00809', '0.00596', '0.02632', '-0.00248', '-0.0008345', '-0.01979', '-0.000924', '0.00585']",,,,,,,
mondo:0014915,short-rib thoracic dysplasia 16 with or without polydactyly,"['short-rib thoracic dysplasia 16 with or without polydactyly', 'SRTD16']",,617102,,C4310718,,,,,,,,
mondo:0014916,"developmental and epileptic encephalopathy, 41","['EIEE41', 'SLC1A2 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, type 41', 'early infantile epileptic encephalopathy caused by mutation in SLC1A2', 'developmental and epileptic encephalopathy 41', 'DEE41', 'epileptic encephalopathy, early infantile, 41']",0080442,617105,,C4310717,,,,,,,,
mondo:0014917,"developmental and epileptic encephalopathy, 42","['early infantile epileptic encephalopathy caused by mutation in CACNA1A', 'epileptic encephalopathy, early infantile, type 42', 'epileptic encephalopathy, early infantile, 42', 'developmental and epileptic encephalopathy 42', 'EIEE42', 'CACNA1A early infantile epileptic encephalopathy', 'DEE42']",0080454,617106,,C4310716,,,,,,,,
mondo:0014918,tall stature-intellectual disability-renal anomalies syndrome,"['TROFAS', 'Thauvin-robinet-Faivre syndrome', 'THAUVIN-robinet-Faivre syndrome']",,617107,500095,C4310715,,,,,,,,
mondo:0014919,sessile serrated polyposis cancer syndrome,"['sessile serrated polyposis cancer syndrome', 'SSPCS']",,617108,,C4310714,,,,,,,,
mondo:0014920,patterned macular dystrophy 3,"['MDPT3', 'patterned macular dystrophy type 3', 'patterned macular dystrophy caused by mutation in MAPKAPK3', 'Martinique crinkled retinal pigment epitheliopathy', 'macular dystrophy, patterned, type 3', 'MAPKAPK3 patterned macular dystrophy', 'macular dystrophy, patterned, 3', 'MCRPE']",0060865,617111,466718,C4310713,,,,,,H35.5,,
mondo:0014921,"developmental and epileptic encephalopathy, 43","['early infantile epileptic encephalopathy caused by mutation in GABRB3', 'EIEE43', 'developmental and epileptic encephalopathy 43', 'DEE43', 'epileptic encephalopathy, early infantile, type 43', 'GABRB3 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 43']",0080447,617113,,C4310712,,,,,,,,
mondo:0014922,myofibrillar myopathy 7,"['KY myofibrillar myopathy (disease)', 'alpha-b crystalin-related fatal infantile hypertonic myofibrillar myopathy', 'myopathy, myofibrillar, type 7', 'myopathy, myofibrillar, 7', 'MFM7']",0080098,617114,,C4310711,,,,,,,,
mondo:0014923,peeling skin syndrome 5,"['peeling skin syndrome caused by mutation in SERPINB8', 'PSS5', 'SERPINB8 peeling skin syndrome', 'peeling skin syndrome type 5', 'peeling skin syndrome 5']",,617115,,C4310710,,,,,,,,
mondo:0014924,"epilepsy, familial focal, with variable foci 2","['epilepsy, familial focal, with variable foci caused by mutation in NPRL2', 'NPRL2 epilepsy, familial focal, with variable foci', 'FFEVF2', 'epilepsy, familial focal, with variable foci type 2', 'epilepsy, familial focal, with variable foci 2']",,617116,,C4310709,,,,,,,,
mondo:0014925,"epilepsy, familial focal, with variable foci 3","['epilepsy, familial focal, with variable foci caused by mutation in NPRL3', 'NPRL3 epilepsy, familial focal, with variable foci', 'epilepsy, familial focal, with variable foci 3', 'epilepsy, familial focal, with variable foci type 3', 'FFEVF3']",,617118,,C4310708,,,,,,,,
mondo:0014926,Bardet-Biedl syndrome 22,"['BBS20', 'Bardet-Biedl syndrome type 20', 'Bardet-Biedl syndrome caused by mutation in IFT74', 'IFT74 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome 20; BBS20']",0081011,617119,,C4310707,,,,,,,,
mondo:0014927,Joubert syndrome 27,"['Joubert syndrome caused by mutation in B9D1', 'Joubert syndrome 27', 'B9D1 Joubert syndrome', 'JBTS27', 'Joubert syndrome type 27']",0110996,617120,,C4310706,,,,,,,,
mondo:0014928,Joubert syndrome 28,"['Joubert syndrome 28', 'Joubert syndrome type 28', 'MKS1 Joubert syndrome', 'Joubert syndrome caused by mutation in MKS1', 'JBTS28']",0110997,617121,,C4310705,,,,,,,,
mondo:0014929,retinitis pigmentosa 76,"['retinitis pigmentosa type 76', 'RP76', 'POMGNT1 retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in POMGNT1', 'retinitis pigmentosa 76']",,617123,,C4310704,,,,,,,,
mondo:0014930,"intellectual disability, autosomal recessive 56","['autosomal recessive non-syndromic intellectual disability caused by mutation in ZC3H14', 'intellectual developmental disorder, autosomal recessive 56', 'ZC3H14 autosomal recessive non-syndromic intellectual disability', 'intellectual disability, autosomal recessive type 56', 'intellectual disability, autosomal recessive 56', 'MRT56', 'mental retardation, autosomal recessive 56', 'mental retardation, autosomal recessive type 56']",0081217,617125,,C4310703,,,,,,,,
mondo:0014931,Alazami-Yuan syndrome,"['Alazami-Yuan syndrome', 'ALYUS']",,617126,,C4310702,"['-0.00842', '0.02168', '0.005512', '0.006092', '0.01349', '-0.02411', '0.00266', '0.02103', '-0.0269', '-0.02078', '-0.00973', '-0.01006', '0.006115', '0.01857', '-0.01439', '-0.006588', '-0.011246', '-0.01111', '-0.01915', '-0.03708', '0.00516', '-0.01504', '0.00676', '-0.00799', '0.00515', '-0.005592', '-0.00964', '-0.01381', '0.01139', '-0.00963', '0.01185', '0.003008', '0.02393', '0.01533', '0.01637', '-0.01689', '0.00435', '-0.01672', '-0.001349', '-0.015305', '0.009', '-0.01657', '0.01188', '-0.008125', '-0.0005884', '-0.02284', '-0.00598', '0.01729', '0.00235', '-0.005894', '-0.01355', '0.00832', '0.004105', '-0.00804', '-0.00207', '0.001621', '0.02562', '0.01061', '-0.03314', '-0.008156', '0.01274', '0.00228', '-0.004303', '-0.00346', '0.003632', '0.00849', '0.0279', '0.02213', '-0.02725', '0.02773', '-0.02596', '-0.004528', '-0.002542', '-0.02011', '-0.000738', '0.004227', '0.008415', '-0.007336', '-0.012856', '-0.001572', '0.005116', '0.00956', '-0.007206', '0.014145', '0.004707', '-0.00791', '0.010086', '0.01744', '0.02925', '-0.001398', '0.009346', '0.014946', '0.006245', '0.01077', '0.03488', '0.01002', '0.01659', '-0.02678', '-0.0082', '0.01325']",,,,,,,
mondo:0014932,orofaciodigital syndrome XV,"['oral-Facial-digital syndrome, type 15', 'Ofds 15', 'orofaciodigital syndrome 15', 'orofaciodigital syndrome type XV', 'OFD15', 'orofaciodigital syndrome XV']",,617127,,C4310701,,,,,,,,
mondo:0014933,"developmental and epileptic encephalopathy, 44","['epileptic encephalopathy, early infantile, 44', 'early infantile epileptic encephalopathy caused by mutation in UBA5', 'DEE44', 'epileptic encephalopathy, early infantile, type 44', 'UBA5 early infantile epileptic encephalopathy', 'EIEE44', 'developmental and epileptic encephalopathy 44']",0080424,617132,,C4310700,,,,,,,,
mondo:0014934,"spinocerebellar ataxia, autosomal recessive 24","['autosomal dominant cerebellar ataxia caused by mutation in UBA5', 'spinocerebellar ataxia, autosomal recessive type 24', 'SCAR24', 'spinocerebellar ataxia, autosomal recessive 24', 'UBA5 autosomal dominant cerebellar ataxia']",0111615,617133,,C4310699,,,,,,,,
mondo:0014935,frontometaphyseal dysplasia 2,"['MAP3K7 frontometaphyseal dysplasia', 'frontometaphyseal dysplasia caused by mutation in MAP3K7', 'Frontometaphyseal dysplasia type 2', 'Frontometaphyseal dysplasia 2', 'FMD2']",0111787,617137,,C4310697,,,,,,,,
mondo:0014936,ZTTK syndrome,"['brain malformations-musculoskeletal abnormalities-facial dysmorphism-intellectual disability syndrome', 'ZTTK multiple congenital anomalies-intellectual disability syndrome', 'Zhu-Tokita-Takenouchi-Kim syndrome', 'ZTTK multiple congenital anomalies-mental retardation syndrome', 'Tokita-Kim syndrome', 'TOKIMS', 'ZTTKS', 'ZTTK syndrome']",,617140,500150,C4310696,,,,,,,,
mondo:0014937,aniridia 2,"['aniridia 2', 'AN2', 'aniridia type 2']",,617141,,,,,,C536372,,,,
mondo:0014938,aniridia 3,"['aniridia 3', 'TRIM44 isolated aniridia', 'isolated aniridia caused by mutation in TRIM44', 'aniridia type 3', 'AN3']",,617142,,,,,,,,,,
mondo:0014939,congenital myasthenic syndrome 20,"['congenital myasthenic syndrome type 20', 'CMS20', 'congenital myasthenic syndrome 20 presynaptic', 'SLC5A7 congenital myasthenic syndrome', 'myasthenic syndrome, congenital, 20, presynaptic', 'congenital myasthenic syndrome caused by mutation in SLC5A7']",0110661,617143,,C4310694,,,,,,,,
mondo:0014940,"neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset","['neurodegeneration with ataxia, dystonia, and gaze palsy, childhood-onset', 'NADGP']",0081364,617145,,C4310693,"['-0.0798', '0.1693', '0.03192', '-0.10345', '-0.01727', '-0.2214', '0.04355', '0.119', '-0.171', '-0.03494', '-0.07074', '-0.05127', '-0.05487', '-0.0676', '0.0836', '-0.1412', '-0.01839', '-0.1652', '-0.0942', '-0.2756', '0.0324', '-0.066', '-0.0243', '-0.01537', '0.001765', '-0.07355', '0.066', '-0.067', '-0.0589', '0.02016', '0.02048', '0.10144', '0.1566', '0.04996', '0.001208', '-0.003778', '-0.05365', '-0.0759', '-0.11664', '-0.09515', '0.0479', '-0.1996', '-0.03955', '0.03114', '0.04153', '-0.1743', '-0.05856', '0.1398', '0.02176', '0.006428', '-0.0006113', '0.09576', '-0.04953', '-0.05002', '0.05127', '-0.0869', '0.11206', '-0.0745', '-0.11505', '0.0563', '0.0381', '0.0584', '0.0697', '0.03418', '-0.14', '-0.00196', '0.1088', '0.10645', '-0.06757', '0.1554', '-0.0595', '0.01492', '-0.01814', '-0.1276', '0.05264', '0.05405', '0.12415', '0.0096', '-0.08484', '-0.03644', '0.012695', '-0.08936', '-0.0205', '0.1848', '-0.003473', '-0.01522', '-0.075', '0.05228', '0.1581', '-0.005806', '0.1334', '0.1158', '0.04785', '0.05643', '0.192', '0.1178', '0.1257', '-0.002064', '0.0767', '0.0665']",,,,,,,
mondo:0014941,"arthrogryposis, distal, with impaired proprioception and touch","['DAIPT', 'arthrogryposis, distal, with impaired proprioception and touch']",,617146,,C4310692,,,,,,,,
mondo:0014942,"developmental and epileptic encephalopathy, 45","['epileptic encephalopathy, early infantile, type 45', 'EIEE45', 'epileptic encephalopathy, early infantile, 45', 'developmental and epileptic encephalopathy 45', 'GABRB1 early infantile epileptic encephalopathy', 'early infantile epileptic encephalopathy caused by mutation in GABRB1', 'DEE45']",0080428,617153,,C4310691,,,,,,,,
mondo:0014943,mitochondrial DNA depletion syndrome 15 (hepatocerebral type),"['MTDPS15', 'TFAM mitochondrial DNA depletion syndrome', 'mitochondrial DNA depletion syndrome 15 (hepatocerebral type)', 'mitochondrial DNA depletion syndrome caused by mutation in TFAM']",0080337,617156,,C4310690,,,,,,,,
mondo:0014944,short stature-brachydactyly-obesity-global developmental delay syndrome,"['SBIDDS', 'short stature, brachydactyly, intellectual developmental disability, and seizures']",,617157,464288,C4310689,"['-0.03806', '0.04776', '0.04337', '-0.0427', '0.03812', '-0.07166', '0.01221', '0.10254', '-0.06854', '-0.05505', '-0.0251', '-0.02103', '0.01531', '0.02441', '-0.03214', '-0.02252', '0.01363', '-0.04642', '-0.03683', '-0.1494', '0.00827', '-0.001711', '0.0417', '-0.0468', '0.02063', '-0.01648', '-0.00607', '-0.007133', '0.01569', '-0.03806', '0.04718', '-0.02574', '0.0983', '0.0461', '0.002844', '-0.02367', '-0.01718', '-0.03986', '-0.02798', '-0.07007', '0.03494', '-0.0686', '0.02174', '-0.01306', '-0.01979', '-0.0662', '-0.02324', '0.04703', '0.0181', '0.01654', '-0.03406', '-0.00845', '0.005135', '-0.002928', '-0.0223', '-0.03934', '0.0193', '-0.02444', '-0.07416', '0.03198', '0.03986', '0.01029', '-0.01599', '0.009796', '0.005184', '-0.007713', '0.05386', '0.06018', '-0.0788', '0.0688', '-0.066', '0.0269', '0.0323', '-0.05215', '0.006092', '0.02559', '0.03577', '-0.02289', '-0.0489', '-0.04306', '-0.002222', '0.002247', '-0.03583', '0.08734', '-0.0006747', '0.0251', '-0.002178', '0.05942', '0.1171', '0.03574', '0.03123', '0.0915', '-0.006294', '0.02777', '0.1263', '0.01427', '0.0663', '-0.08905', '0.02896', '0.04938']",,,,,,,
mondo:0014945,"myopathy, distal, with rimmed vacuoles","['myopathy, distal, with rimmed vacuoles', 'DMRV']",0081363,617158,,CN239822,,,,,,,,
mondo:0014946,Sifrim-Hitz-Weiss syndrome,"['Sifrim-Hitz-Weiss syndrome', 'SIHIWES', 'Sifrim-Hitz-Weiss multiple congenital anomalies-mental retardation syndrome', 'Sifrim-Hitz-Weiss multiple congenital anomalies-intellectual disability syndrome']",,617159,,C4310688,"['-0.02095', '0.02069', '0.010124', '-0.014755', '0.01029', '-0.06165', '0.001653', '0.0371', '-0.0464', '-0.0456', '-0.0102', '-0.00452', '0.005253', '0.0106', '-0.02338', '-0.02203', '0.011894', '-0.00205', '-0.01944', '-0.06415', '-0.002712', '-0.011795', '0.02937', '-0.02534', '0.02095', '-0.01536', '-0.02524', '-0.0145', '0.02902', '-0.03323', '0.02977', '-0.01424', '0.03714', '0.02586', '0.004333', '-0.02168', '-0.01401', '-0.03076', '0.001213', '-0.03766', '0.02356', '-0.03638', '0.0004358', '-0.0252', '0.013916', '-0.0457', '-0.02612', '0.02795', '0.01494', '0.006832', '-0.002241', '-0.00794', '0.009926', '-0.01584', '-0.02196', '-0.0343', '0.03506', '-0.01872', '-0.03467', '0.004513', '0.01733', '0.004066', '0.003548', '-0.003914', '-0.003735', '-0.00823', '0.05328', '0.02542', '-0.0342', '0.04733', '-0.0437', '-0.003687', '0.009674', '-0.02531', '0.02565', '0.0187', '0.013794', '0.00454', '-0.03635', '-0.02058', '-0.001315', '0.006718', '-0.00986', '0.03348', '-0.01495', '-0.005123', '0.002203', '0.05533', '0.0448', '0.01743', '0.0178', '0.04227', '0.00969', '0.008865', '0.08026', '0.00959', '0.0426', '-0.0714', '-0.003819', '0.02681']",,,,,,,
mondo:0014947,"developmental and epileptic encephalopathy, 46","['developmental and epileptic encephalopathy 46', 'epileptic encephalopathy, early infantile, 46', 'EIEE46', 'epileptic encephalopathy, early infantile, type 46', 'early infantile epileptic encephalopathy caused by mutation in GRIN2D', 'GRIN2D early infantile epileptic encephalopathy', 'DEE46']",0080456,617162,,C4310687,,,,,,,,
mondo:0014948,"short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay","['short stature, rhizomelic, with microcephaly, micrognathia, and developmental delay', 'SRMMD']",,617164,,C4310686,"['-0.1131', '0.12225', '0.0997', '-0.11664', '0.0642', '-0.1078', '0.02516', '0.22', '-0.1736', '-0.08527', '-0.00905', '0.00896', '-0.00224', '0.00673', '-0.0452', '-0.01668', '0.06055', '-0.05603', '-0.10376', '-0.2448', '0.006435', '-0.002419', '0.0969', '-0.06216', '0.05847', '-0.0374', '-0.01826', '-0.003515', '0.00512', '-0.0535', '0.05215', '-0.05072', '0.1619', '0.09717', '0.06107', '0.003183', '-0.01344', '-0.05896', '-0.02806', '-0.1169', '0.0506', '-0.1405', '-0.00403', '-0.01307', '-0.0683', '-0.113', '0.0003107', '0.1254', '0.00992', '0.0247', '-0.07117', '-0.03644', '-0.00718', '0.03314', '-0.04782', '-0.1086', '-0.01562', '-0.0761', '-0.0874', '0.05783', '0.0447', '0.04968', '-0.06537', '0.0578', '0.005', '-0.02246', '0.08563', '0.1348', '-0.1431', '0.146', '-0.1179', '0.07635', '0.0817', '-0.09705', '-0.02052', '0.0397', '0.04993', '-0.1105', '-0.06866', '-0.05347', '0.00988', '0.02365', '-0.0691', '0.1342', '-0.005154', '0.06058', '-0.01724', '0.1212', '0.1844', '0.0705', '0.01675', '0.1282', '-0.01206', '0.02391', '0.2283', '0.05087', '0.1279', '-0.1287', '0.0986', '0.082']",,,,,,,
mondo:0014949,"developmental and epileptic encephalopathy, 47","['FGF12 early infantile epileptic encephalopathy', 'developmental and epileptic encephalopathy 47', 'early infantile epileptic encephalopathy caused by mutation in FGF12', 'DEE47', 'EIEE47', 'epileptic encephalopathy, early infantile, 47', 'epileptic encephalopathy, early infantile, type 47']",0080425,617166,,C4310685,,,,,,,,
mondo:0014950,"aortic aneurysm, familial thoracic 10","['AAT10', 'aortic aneurysm, familial thoracic type 10', 'familial thoracic aortic aneurysm and aortic dissection caused by mutation in LOX', 'aortic aneurysm, familial thoracic 10', 'LOX familial thoracic aortic aneurysm and aortic dissection']",,617168,,C4284414,,,,,,,,
mondo:0014951,"intellectual developmental disorder, autosomal recessive 74","['intellectual developmental disorder, autosomal recessive 74', 'Sotos syndrome caused by mutation in APC2', 'Sotos syndrome type 3', 'APC2 Sotos syndrome', 'SOTOS3', 'Sotos syndrome 3']",0112104,617169,,C4310684,,,,,,,,
mondo:0014952,intellectual disability-epilepsy-extrapyramidal syndrome,"['DYSEIDD', 'neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures', 'dyskinesia, seizures, and intellectual developmental disorder']",,617171,468620,C4310683,,,,,,,,
mondo:0014953,gnb5-related intellectual disability-cardiac arrhythmia syndrome,"['intellectual developmental disorder with cardiac arrhythmia', 'IDDCA']",0081008,617173,542306,C4310682,"['-0.02872', '0.04355', '0.04398', '-0.0326', '0.03076', '-0.08606', '0.01558', '0.11523', '-0.0459', '-0.0488', '-0.03952', '-0.02608', '0.008606', '0.006603', '-0.02713', '-0.03156', '-0.0366', '-0.0176', '-0.05328', '-0.1459', '0.01877', '-0.005424', '0.04987', '-0.01984', '0.0266', '-0.04233', '-0.02255', '-0.00969', '0.022', '-0.0381', '0.0659', '-0.02432', '0.0911', '0.03854', '0.009285', '-0.03864', '0.008385', '-0.0249', '-0.0218', '-0.05884', '0.03001', '-0.0677', '0.02155', '-0.01376', '0.005558', '-0.0571', '-0.0284', '0.05383', '0.00479', '0.02278', '-0.04263', '0.03882', '0.014145', '-0.00795', '-0.04083', '-0.02', '0.0467', '-0.0223', '-0.06885', '0.007217', '0.05203', '0.0163', '0.002846', '-0.000142', '-0.01217', '0.01537', '0.0411', '0.0854', '-0.07574', '0.06354', '-0.07367', '0.001048', '0.00804', '-0.04807', '0.004658', '0.0492', '0.0336', '-0.01971', '-0.04697', '-0.01782', '0.01331', '-0.001379', '-0.04453', '0.07983', '0.001512', '0.0241', '0.01689', '0.0755', '0.0803', '0.05814', '0.02823', '0.0538', '-0.00364', '0.03113', '0.1339', '0.05875', '0.07153', '-0.0937', '-0.00977', '0.03995']",,,,,,,
mondo:0014954,"Ehlers-Danlos syndrome, periodontal type 2","['EDSPD2', 'Ehlers-Danlos syndrome, periodontal type, 2']",0080987,617174,,,,,,,,,,
mondo:0014955,RCBTB1-related retinopathy,"['RCBTB1-related retinopathy', 'retinal dystrophy with or without extraocular anomalies', 'RDEOA']",,617175,,C4310680,,,,,,,,
mondo:0014956,Chitayat syndrome,"['Chitayat syndrome', 'CHYTS']",,617180,,C4310679,"['0.0007324', '0.00946', '0.00798', '0.002535', '0.00923', '-0.012596', '0.0004845', '0.02206', '-0.01857', '-0.004124', '-0.005253', '0.006794', '-0.001581', '-0.004932', '0.002', '-0.01862', '0.003456', '-0.001242', '-0.005497', '-0.02649', '-2.193e-05', '-0.001937', '0.01846', '-0.002316', '-0.002712', '-0.002249', '-0.01363', '0.0003054', '0.004307', '-0.01843', '0.00642', '0.006443', '0.0172', '0.015114', '-0.005356', '-0.00924', '0.000866', '-0.006557', '-0.002256', '-0.01819', '0.00809', '-0.008575', '0.007343', '-0.00438', '0.0091', '-0.02019', '-0.01494', '0.003698', '0.00886', '-0.00551', '-0.01534', '0.002758', '0.002308', '0.01194', '-0.004543', '-0.01099', '0.01888', '0.000674', '-0.02548', '-0.00683', '0.00795', '0.0021', '0.00483', '-0.003855', '0.001203', '0.0083', '0.02579', '0.005333', '-0.01701', '0.00901', '-0.02023', '0.003881', '-0.001492', '-0.01695', '0.0069', '0.01376', '-0.004925', '0.00942', '-0.01845', '-0.007145', '-0.003937', '0.006264', '-0.01304', '0.01065', '0.005074', '0.006813', '0.005173', '0.0124', '0.02138', '0.006004', '-0.0001071', '0.01587', '-0.001959', '0.000756', '0.0292', '0.004658', '0.02254', '-0.01953', '-0.002766', '0.00547']",,,,,,,
mondo:0014957,language delay and attention deficit-hyperactivity disorder/cognitive impairment with or without cardiac arrhythmia,"['language delay and attention Deficit-hyperactivity disorder/cognitive impairment with or without Cardiac arrhythmia', 'LADCI', 'language delay and ADHD/cognitive impairment with or without cardiac arrhythmia']",,617182,,C4310678,"['-0.0694', '0.0891', '0.09906', '-0.1071', '0.002516', '-0.139', '0.0838', '0.2397', '-0.1469', '-0.05206', '-0.1201', '-0.11115', '0.02309', '0.03497', '-0.009094', '-0.06232', '-0.0918', '-0.0996', '-0.1373', '-0.2695', '0.04196', '0.03235', '0.03726', '-0.00922', '0.0797', '-0.0926', '0.01136', '-0.02658', '0.015366', '-0.06125', '0.0645', '-0.0397', '0.1833', '0.0695', '-0.012', '-0.0511', '-0.0383', '-0.0812', '-0.04663', '-0.1512', '0.0866', '-0.133', '0.0679', '0.0002627', '0.02051', '-0.06744', '-0.04745', '0.09875', '-0.10486', '0.1404', '-0.0946', '0.1283', '-0.01147', '0.0444', '0.000542', '0.0003493', '0.06464', '-0.06198', '-0.1647', '0.04797', '0.1088', '0.05997', '0.0183', '0.02208', '-0.0215', '0.01344', '0.08704', '0.1567', '-0.10156', '0.1257', '-0.12006', '0.05655', '-0.02705', '-0.0864', '0.02542', '0.0433', '0.0827', '-0.08777', '-0.12476', '-0.0876', '0.05884', '-0.02757', '-0.07684', '0.1835', '0.006165', '0.0753', '-0.02136', '0.1283', '0.1741', '0.0838', '0.0986', '0.1132', '-0.02892', '0.06125', '0.2235', '0.09155', '0.1123', '-0.1598', '0.03177', '0.1343']",,,,,,,
mondo:0014958,Harel-Yoon syndrome,"['HAYOS', 'optic atrophy-peripheral neuropathy-developmental delay syndrome', 'Harel-Yoon syndrome']",,617183,496790,C4310677,"['-0.00798', '-0.001621', '0.003452', '0.00778', '-0.008415', '-0.0006657', '0.009155', '0.0013685', '-0.01341', '-0.00878', '-0.00425', '-0.00861', '-0.002798', '-0.004646', '-0.0001569', '-0.01067', '-0.002329', '0.006634', '-0.0009623', '-0.01235', '-0.003983', '0.0006857', '-0.003967', '0.003555', '0.00719', '-0.00463', '0.001193', '-0.001588', '-0.00246', '0.006256', '0.01023', '-0.007084', '0.014984', '0.0004525', '-0.00438', '0.002888', '0.006355', '-0.000489', '-0.0015545', '-0.002983', '0.009926', '-0.01245', '-0.000271', '0.0001007', '0.002588', '-0.007793', '0.004414', '-0.00801', '0.002438', '0.005733', '-0.00826', '0.008415', '0.01045', '-0.00755', '-0.007275', '0.002829', '0.001374', '-0.00196', '0.0005326', '-0.00886', '0.00269', '-0.00885', '0.00554', '0.008934', '-0.00882', '0.00127', '0.00866', '0.00426', '0.000716', '0.007683', '-0.002558', '-0.003376', '-0.006935', '0.003084', '-0.007442', '-0.001682', '-0.0028', '-0.0094', '0.001658', '-0.002197', '0.005856', '-0.0046', '-0.006264', '0.001557', '-0.005264', '0.001518', '-0.00813', '0.01069', '-0.002586', '-0.0004265', '-0.001208', '-0.005665', '0.00866', '-0.0039', '0.00556', '0.01079', '-0.00519', '-0.01006', '-0.004894', '0.00977']",,,,,,,
mondo:0014959,"mitochondrial DNA depletion syndrome 12A (cardiomyopathic type), autosomal dominant","['mitochondrial DNA depletion syndrome 12A (cardiomyopathic type) AD', 'mitochondrial DNA depletion syndrome 12a (cardiomyopathic type), autosomal dominant', 'MTDPS12A']",0080130,617184,,C4310676,,,,,,,,
mondo:0014960,"encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy","['encephalopathy, progressive, early-onset, with brain oedema and/or leukoencephalopathy; PEBEL', 'encephalopathy, progressive, early-onset, with brain edema and/or leukoencephalopathy', 'PEBEL']",,,,C4310675,,,,,,,,
mondo:0014961,spermatogenic failure 16,"['azoospermia caused by mutation in SUN5', 'SUN5 azoospermia', 'spermatogenic failure type 16', 'spermatogenic failure 16', 'acephalic spermatozoa syndrome', 'SPGF16']",0070184,617187,,C4310674,,,,,,,,
mondo:0014962,"intellectual disability, autosomal recessive 57","['mental retardation, autosomal recessive 57', 'intellectual disability, autosomal recessive 57', 'MBOAT7 autosomal recessive non-syndromic intellectual disability', 'autosomal recessive non-syndromic intellectual disability caused by mutation in MBOAT7', 'intellectual developmental disorder, autosomal recessive 57', 'mental retardation, autosomal recessive type 57', 'MRT57', 'intellectual disability, autosomal recessive type 57']",0081219,617188,,C4310673,,,,,,,,
mondo:0014963,Shashi-Pena syndrome,"['SHAPNS', 'Shashi-Pena syndrome']",,617190,,C4310672,"['-0.00877', '0.00914', '0.0096', '-0.003078', '0.00782', '9.555e-05', '-0.005142', '0.01256', '-0.0001956', '-0.01087', '-0.00686', '-0.002302', '0.00669', '0.00994', '-0.006176', '-0.008064', '0.007713', '-0.00895', '-0.0008283', '-0.02304', '-0.00833', '-0.008514', '0.013374', '-0.01114', '0.00291', '-0.001397', '-0.01128', '0.00672', '-0.004864', '0.002502', '-0.001733', '-0.007587', '0.012085', '0.005634', '0.00919', '-0.01216', '-0.004314', '-0.001613', '0.00886', '-0.004623', '-0.004894', '0.002901', '0.003178', '-0.01252', '-0.002188', '-0.002695', '-0.002567', '0.006016', '-0.00493', '-0.00393', '-0.0107', '-0.003695', '-0.00508', '0.003551', '-0.003952', '0.00457', '0.01462', '-0.006226', '0.002787', '-0.0071', '0.004704', '-0.00337', '0.007767', '-0.002869', '0.007866', '-0.003117', '0.01665', '0.01474', '0.00064', '0.008766', '-0.01309', '0.00939', '0.007275', '-0.0008907', '-0.002182', '-0.001004', '0.00928', '0.005722', '-0.001484', '-0.003223', '0.002007', '-0.00224', '-0.000662', '0.00451', '0.0052', '-0.004093', '-0.003115', '0.01176', '0.000951', '0.01185', '0.01023', '0.0006976', '0.004574', '-0.001561', '0.01129', '0.00622', '-2.533e-05', '-0.01875', '-0.00212', '0.010574']",,,,,,,
mondo:0014965,lethal congenital contracture syndrome 11,"['lethal congenital contracture syndrome type 11', 'GLDN lethal congenital contracture syndrome', 'LCCS11', 'lethal congenital contracture arthrogryposis-11', 'lethal congenital contracture syndrome 11', 'lethal congenital contracture syndrome caused by mutation in GLDN']",,617194,,C4310670,,,,,,,,
mondo:0014966,periventricular nodular heterotopia 7,"['periventricular nodular heterotopia type 7', 'NEDD4L periventricular nodular heterotopia', 'periventricular nodular heterotopia 7', 'PVNH7', 'periventricular nodular heterotopia caused by mutation in NEDD4L']",,617201,,C4310669,,,,,,,,
mondo:0014967,"heterotaxy, visceral, 8, autosomal","['visceral heterotaxy caused by mutation in PKD1L1', 'PKD1L1 visceral heterotaxy', 'heterotaxy, visceral, 8, autosomal', 'HTX8']",,617205,,C4310668,,,,,,,,
mondo:0014968,"encephalopathy, progressive, with amyotrophy and optic atrophy","['PEAMO', 'encephalopathy, progressive, with amyotrophy and optic atrophy']",,617207,,C4310667,"['-0.02802', '0.05246', '0.01651', '-0.01698', '0.00653', '-0.06122', '0.002678', '0.069', '-0.0704', '-0.01622', '-0.02176', '-0.02461', '-0.00865', '0.0004287', '-0.01437', '-0.0366', '0.01247', '-0.0117', '-0.01079', '-0.0883', '0.002861', '-0.03918', '0.02725', '-0.003082', '0.004486', '-0.01366', '0.0006647', '-0.01426', '-0.01515', '-0.01424', '0.03738', '0.004147', '0.04172', '0.01698', '0.0144', '-0.007244', '-0.013885', '-0.02142', '-0.004642', '-0.03305', '0.01787', '-0.064', '0.007336', '0.005135', '-0.004208', '-0.04523', '-0.002872', '0.03035', '-0.001233', '0.0174', '-0.0242', '0.008675', '-0.0002062', '-0.000861', '-0.01421', '-0.010376', '0.05338', '-0.0183', '-0.0709', '0.02528', '0.003618', '0.01784', '0.001047', '0.02507', '-0.0347', '0.007183', '0.05505', '0.07294', '-0.02725', '0.071', '-0.04507', '0.02438', '0.02539', '-0.03244', '0.014755', '0.0236', '0.00747', '-0.0003297', '-0.02507', '-0.02626', '0.00629', '-0.00051', '-0.00483', '0.0513', '-0.01326', '0.0006785', '0.014206', '0.04388', '0.0578', '0.00526', '0.02382', '0.0477', '0.0004606', '0.00564', '0.08777', '0.0332', '0.04932', '-0.03053', '-0.003426', '0.02422']",,,,,,,
mondo:0014969,isolated sedoheptulokinase deficiency,"['isolated SHPK deficiency', 'SHPKD', 'sedoheptulokinase deficiency']",,617213,440713,C1291373,,,,,277.6,,,
mondo:0014970,spermatogenic failure 17,"['spermatogenic failure type 17', 'SPGF17', 'Male infertility due to oocyte Activation failure', 'PLCZ1 azoospermia', 'spermatogenic failure 17', 'azoospermia caused by mutation in PLCZ1']",0070174,617214,,C4310666,,,,,,,,
mondo:0014971,"amelogenesis imperfecta, hypomaturation type, IIa6","['AI2A6', 'amelogenesis imperfecta, hypomaturation type, IIa6']",0080960,617217,,C4310665,,,,,,,,
mondo:0014972,"chromosome 19q13.11 deletion syndrome, proximal",,,617219,,C4311046,,,,,,,,
mondo:0014973,"sudden cardiac failure, infantile","['SCFI', 'sudden Cardiac failure, infantile']",,617222,,C4310664,,,,,,,,
mondo:0014974,"sudden cardiac failure, alcohol-induced","['sudden Cardiac failure, alcohol-induced', 'SCFAI']",,617223,,C4310663,,,,,,,,
mondo:0014975,autosomal recessive spastic paraplegia type 78,"['hereditary spastic paraplegia caused by mutation in ATP13A2', 'spastic paraplegia 78, autosomal recessive', 'ATP13A2 hereditary spastic paraplegia', 'SPG78']",0112348,617225,513436,C4310662,,,,,,,,
mondo:0014976,lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome,"['COXPD31', 'combined oxidative phosphorylation deficiency type 31', 'combined oxidative phosphorylation deficiency caused by mutation in MIPEP', 'MIPEP combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 31']",0111488,617228,478049,C4310661,,,,,,,,
mondo:0014977,autosomal recessive limb-girdle muscular dystrophy type 2R1,"['limb-girdle muscular dystrophy type 2Z', 'muscular dystrophy, limb-girdle, autosomal recessive 21', 'LGMD2Z', 'POGLUT1 autosomal recessive limb-girdle muscular dystrophy', 'autosomal recessive limb-girdle muscular dystrophy type 2Z', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in POGLUT1', 'muscular dystrophy, limb-girdle, type 2Z']",0080762,617232,480682,CN776834,,C142082,,,,,,
mondo:0014979,"myoclonus, intractable, neonatal","['NEIMY', 'myoclonus, intractable, neonatal']",,617235,,C4310658,,,,,,,,
mondo:0014980,cone-rod dystrophy and hearing loss,"['cone-rod dystrophy and hearing loss', 'CRDHL']",,,,C4310657,"['0.7686', '0.128', '0.3767', '0.784', '-0.518', '0.0511', '0.996', '0.7954', '-0.1721', '-0.723', '0.1731', '0.2056', '-0.708', '0.4226', '-0.3684', '-0.8223', '-0.591', '0.2164', '-0.4385', '-0.301', '0.0654', '0.1788', '-0.688', '0.3245', '0.95', '0.0661', '-0.9385', '0.02245', '-0.7896', '-0.0707', '0.04233', '-0.2744', '0.02705', '-0.2307', '-0.3833', '-0.3684', '-0.5586', '-0.617', '-0.1166', '-1.046', '-0.05725', '0.01346', '0.00753', '-0.2457', '0.0798', '-0.768', '0.02376', '0.2705', '0.2173', '-0.1763', '-0.07874', '-0.4375', '-0.2411', '0.16', '0.3218', '0.8076', '0.285', '0.2844', '-0.4292', '0.4314', '-0.2479', '1.091', '-0.2366', '0.3826', '-0.4539', '0.3203', '-0.5483', '0.907', '-0.4827', '-0.2922', '0.1066', '0.709', '1.1', '-1.042', '0.4282', '0.05536', '0.8887', '0.5522', '0.1785', '-0.3042', '0.0758', '-0.8745', '-0.7275', '0.8135', '0.118', '-0.3772', '-0.1885', '1.49', '0.2026', '0.7007', '0.2551', '0.1863', '-0.04456', '0.708', '0.4834', '0.02502', '-0.3198', '-1.297', '-0.5347', '-0.08856']",,0009151,,,,,
mondo:0014981,immunodeficiency 49,"['primary immunodeficiency disease caused by mutation in BCL11B', 'immunodeficiency 49', 'SCID, T cell-Negative, B cell-Positive, Nk cell-Positive, with intellectual disability, spasticity, and craniofacial abnormalities', 'immunodeficiency type 49', 'BCL11B primary immunodeficiency disease', 'severe combined immunodeficiency, T cell-Negative, B cell-Positive, Nk cell-Positive, with intellectual disability, spasticity, and craniofacial abnormalities', 'IMD49']",0111979,617237,,C4310656,,,,,,,,
mondo:0014982,"myopia 25, autosomal dominant","['MYP25', 'P4HA2 myopia (disease)', 'myopia 25, autosomal dominant']",,617238,,C4310655,,,,,,,,
mondo:0014983,congenital myasthenic syndrome 21,"['myasthenic syndrome, congenital, 21, presynaptic', 'SLC18A3 congenital myasthenic syndrome', 'congenital myasthenic syndrome caused by mutation in SLC18A3', 'congenital myasthenic syndrome type 21', 'congenital myasthenic syndrome 21, presynaptic', 'CMS21']",0110672,617239,,C4310654,,,,,,,,
mondo:0014984,"lung disease, immunodeficiency, and chromosome breakage syndrome;","['lung disease, immunodeficiency, and chromosome breakage syndrome', 'LICS']",,617241,,C4310653,,,,,,,,
mondo:0014985,Fanconi anemia complementation group V,"['Fanconi Anemia, complementation group type V', 'FANCV', 'MAD2L2 Fanconi anaemia', 'Fanconi anemia, complementation GROUP V', 'Fanconi anaemia complementation group type V', 'Fanconi anemia caused by mutation in MAD2L2', 'MAD2L2 Fanconi anemia', 'Fanconi anemia complementation group type V', 'Fanconi Anemia, complementation Group 5', 'Fanconi anaemia caused by mutation in MAD2L2', 'Fanconi Anemia, complementation group V']",0111080,617243,,C4310652,,,,,,,,
mondo:0014986,Fanconi anemia complementation group R,"['Fanconi anemia complementation group type R', 'Fanconi Anemia, complementation group R', 'Fanconi anemia caused by mutation in RAD51', 'RAD51 Fanconi anaemia', 'Fanconi anaemia complementation group type R', 'Fanconi Anemia, complementation group type R', 'RAD51 Fanconi anemia', 'Fanconi anemia, complementation GROUP R', 'Fanconi anaemia caused by mutation in RAD51', 'FANCR']",0111090,617244,,C4284093,,,,,,,,
mondo:0014987,Fanconi anemia complementation group U,"['Fanconi anaemia complementation group type U', 'Fanconi anemia complementation group type U', 'Fanconi anemia caused by mutation in XRCC2', 'Fanconi Anemia, complementation group U', 'XRCC2 Fanconi anaemia', 'Fanconi anemia, complementation GROUP U', 'Fanconi Anemia, complementation group type U', 'FANCU', 'Fanconi anaemia caused by mutation in XRCC2', 'XRCC2 Fanconi anemia']",0111085,617247,,C4310651,,,,,,,,
mondo:0014989,uncombable hair syndrome 2,"['uncombable hair syndrome type 2', 'uncombable hair syndrome caused by mutation in TGM3', 'UHS2', 'uncombable hair syndrome 2', 'TGM3 uncombable hair syndrome']",,617251,,C4310649,,,,,,,,
mondo:0014990,uncombable hair syndrome 3,"['uncombable hair syndrome type 3', 'UHS3', 'uncombable hair syndrome 3', 'TCHH uncombable hair syndrome', 'uncombable hair syndrome caused by mutation in TCHH']",,617252,,C4310648,,,,,,,,
mondo:0014991,Seckel syndrome 10,"['Seckel syndrome 10', 'Seckel syndrome caused by mutation in NSMCE2', 'Seckel syndrome type 10', 'SCKL10', 'NSMCE2 Seckel syndrome']",0070008,617253,,C4310647,,,,,,,,
mondo:0014992,lissencephaly 8,"['lissencephaly 8', 'TMTC3 lissencephaly (disease)', 'lissencephaly type 8', 'LIS8']",0112233,617255,,C4310646,,,,,,,,
mondo:0014993,myofibrillar myopathy 8,"['MFM8', 'myopathy, myofibrillar, 8', 'PYROXD1 myofibrillar myopathy (disease)', 'myopathy, myofibrillar, type 8']",0080308,617258,,C4310645,,,,,,,,
mondo:0014994,"global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies","['GDACCF', 'global developmental delay, absent or hypoplastic corpus callosum, and dysmorphic facies']",,617260,,C4310644,"['-0.1543', '0.1263', '0.172', '-0.1777', '0.0691', '-0.0855', '-0.01442', '0.3003', '-0.1968', '-0.1315', '-0.1399', '-0.1022', '0.002151', '-0.0683', '-0.10004', '-0.007336', '0.02048', '-0.1171', '-0.1041', '-0.3235', '0.0757', '0.0119', '0.1506', '-0.0773', '0.0933', '-0.03973', '-0.0161', '0.0632', '0.05862', '-0.1394', '0.1788', '-0.02916', '0.246', '0.0939', '0.08435', '-0.0388', '-0.104', '-0.10876', '-0.03546', '-0.1525', '0.1046', '-0.1238', '-0.02725', '0.0343', '-0.0449', '-0.1704', '-0.01531', '0.106', '-0.056', '0.01484', '-0.0789', '0.01177', '-0.1011', '-0.01359', '-0.1147', '-0.02222', '-0.02086', '-0.1477', '-0.2191', '0.09906', '-0.02939', '0.0683', '-0.04495', '0.0768', '-0.05746', '-0.0329', '0.1267', '0.2085', '-0.1931', '0.2004', '-0.1243', '0.1124', '0.05927', '-0.0547', '-0.0339', '0.0497', '0.2245', '-0.124', '-0.1672', '-0.10596', '0.03796', '-0.007656', '-0.0332', '0.18', '-0.00938', '0.0542', '-0.04608', '0.2155', '0.1974', '0.04105', '0.1141', '0.3071', '0.02791', '0.0703', '0.2964', '0.03084', '0.1705', '-0.1238', '0.2064', '0.1776']",,,,,,,
mondo:0014995,"neurodevelopmental disorder with hypotonia, seizures, and absent language","['neurodevelopmental disorder with hypotonia, seizures, and absent language', 'NDHSAL']",,617268,,C4310643,"['-0.0844', '0.1073', '0.08264', '-0.0984', '-0.01294', '-0.1425', '0.03006', '0.1959', '-0.1381', '-0.04074', '-0.06836', '-0.06445', '0.00956', '-0.01682', '-0.005695', '-0.01933', '0.0408', '-0.08325', '-0.099', '-0.2617', '0.002268', '-0.04938', '0.0875', '-0.05707', '0.10266', '-0.0768', '-0.00904', '-0.02164', '0.000681', '-0.081', '0.05096', '-0.0101', '0.1501', '0.0955', '-0.000214', '-0.02052', '-0.04382', '-0.04697', '-0.05792', '-0.1247', '0.08093', '-0.1224', '-0.01364', '-0.00931', '-0.006287', '-0.1298', '-0.04175', '0.09064', '-0.03375', '0.11273', '-0.1104', '0.03592', '-0.02206', '0.04544', '-0.01685', '0.02963', '0.0693', '-0.05182', '-0.136', '0.07605', '0.04303', '0.0549', '0.04755', '0.04855', '-0.01779', '0.005466', '0.1506', '0.1158', '-0.11584', '0.1327', '-0.1279', '0.0564', '-0.01327', '-0.0761', '0.0222', '0.0328', '0.09436', '-0.06158', '-0.128', '-0.0646', '0.05014', '0.01022', '-0.05014', '0.1383', '0.007732', '0.04727', '-0.02756', '0.11536', '0.1533', '0.07825', '0.03714', '0.1993', '-0.03613', '0.05893', '0.198', '0.101', '0.1017', '-0.1583', '0.05295', '0.0807']",,,,,,,
mondo:0014996,"intellectual disability, autosomal recessive 58","['mental retardation, autosomal recessive 58', 'intellectual disability, autosomal recessive type 58', 'ELP2 autosomal recessive non-syndromic intellectual disability', 'ELP2-related disorder', 'MRT58', 'intellectual disability, autosomal recessive 58', 'autosomal recessive non-syndromic intellectual disability caused by mutation in ELP2', 'intellectual developmental disorder, autosomal recessive 58', 'autosomal recessive intellectual disability 58', 'mental retardation, autosomal recessive type 58']",0081220,617270,,C4310641,,,,,,,,
mondo:0014997,nephronophthisis 20,"['nephronophthisis 20', 'NPHP20', 'MAPKBP1 nephronophthisis (disease)', 'nephronophthisis type 20']",0111127,617271,,C4310640,,,,,,,,
mondo:0014998,"glaucoma 3, primary congenital, E","['glaucoma 3, primary congenital, E', 'glaucoma 3, primary congenital, type E', 'GLC3E']",,617272,,C4310639,,,,,,,,
mondo:0014999,"tooth agenesis, selective, 9","['tooth agenesis caused by mutation in GREM2', 'STHAG9', 'tooth agenesis, selective, type 9', 'tooth agenesis, selective, 9', 'GREM2 tooth agenesis']",,617275,,,,,,,,,,
mondo:0015000,"developmental and epileptic encephalopathy, 48","['early infantile epileptic encephalopathy caused by mutation in AP3B2', 'AP3B2 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 48', 'DEE48', 'developmental and epileptic encephalopathy 48', 'epileptic encephalopathy, early infantile, type 48', 'EIEE48']",0080448,617276,,C4310637,,,,,,,,
mondo:0015001,"atrial fibrillation, familial, 18","['familial atrial fibrillation caused by mutation in MYL4', 'atrial fibrillation, familial, type 18', 'MYL4 familial atrial fibrillation', 'atrial fibrillation, familial, 18', 'ATFB18']",,617280,,C4310636,,,,,,,,
mondo:0015002,"developmental and epileptic encephalopathy, 49","['DENND5A early infantile epileptic encephalopathy', 'EIEE49', 'epileptic encephalopathy, early infantile, type 49', 'developmental and epileptic encephalopathy 49', 'epileptic encephalopathy, early infantile, 49', 'early infantile epileptic encephalopathy caused by mutation in DENND5A', 'DEE49']",0080441,617281,,C4310635,,,,,,,,
mondo:0015003,"dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities","['dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities', 'dystonia 29, childhood-onset', 'DYTOABG']",,617282,508093,C4310634,"['-0.0367', '0.04337', '0.007507', '-0.02486', '0.00715', '-0.05423', '0.009995', '0.0628', '-0.0515', '-0.00755', '-0.010056', '-0.01918', '-0.02232', '0.00238', '-0.01994', '-0.03918', '0.003664', '-0.0363', '-0.01765', '-0.0958', '-0.01528', '-0.02435', '0.02235', '0.0001705', '0.01245', '-0.00615', '0.000979', '0.0004842', '-0.009315', '-0.0307', '0.02594', '-0.001509', '0.0552', '0.01704', '0.003208', '-0.00788', '-0.01428', '-0.01616', '0.00743', '-0.0449', '0.01637', '-0.0597', '0.006634', '0.004246', '0.01549', '-0.0472', '-0.01536', '0.0183', '0.009605', '0.001976', '-0.001187', '-0.0005903', '-0.006477', '-0.005272', '-0.0162', '0.003826', '0.0527', '-0.0128', '-0.05106', '0.002975', '0.01075', '0.003044', '0.01003', '0.003143', '-0.0367', '0.01118', '0.06094', '0.05762', '-0.03775', '0.05612', '-0.03625', '0.01591', '0.007233', '-0.02457', '0.01817', '0.021', '0.00875', '-0.00615', '-0.03041', '-0.02629', '-0.006187', '-0.00241', '-0.001774', '0.04654', '-0.01732', '0.01121', '0.01036', '0.0428', '0.04462', '0.01591', '0.02711', '0.04037', '0.01389', '0.009575', '0.0964', '0.02657', '0.05466', '-0.03885', '0.004486', '0.005264']",,,,,,,
mondo:0015004,"dystonia 28, childhood-onset","['DYT28', 'KMT2B dystonic disorder', 'dystonic disorder caused by mutation in KMT2B', 'dystonia 28, childhood-onset']",,617284,589618,C4310633,,,,,,,,
mondo:0015005,"epilepsy, early-onset, vitamin B6-dependent","['epilepsy, early-onset, vitamin B6-dependent', 'EPVB6D']",0080769,617290,,C4310632,,,,,,,,
mondo:0015006,"epidermolysis bullosa simplex 6, generalized, with scarring and hair loss","['generalized basal epidermolysis bullosa simplex with skin atrophy, scarring and hair loss', 'epidermolysis bullosa simplex, generalized, with scarring and hair loss', 'epidermolysis bullosa simplex 6, generalized, with scarring and hair loss', 'EBSSH', 'generalised basal epidermolysis bullosa simplex with skin atrophy, scarring and hair loss']",,617294,508529,C4310631,,,,,,,,
mondo:0015007,"spastic paraplegia, intellectual disability, nystagmus, and obesity;","['SINO', 'spastic paraplegia, intellectual disability, nystagmus, and obesity']",,617296,521390,C4284592,,,,,,,,
mondo:0015008,"amelogenesis imperfecta, type 1J","['AI1J', 'amelogenesis imperfecta, type Ij', 'amelogenesis imperfecta, type 1J']",0080953,617297,,,,,,,,,,
mondo:0015009,lymphatic malformation 7,"['hydrops fetalis, nonimmune, and/or atrial septal defect, susceptibility to', 'HFASD']",,617300,,,"['-0.1185', '0.073', '0.0976', '-0.1486', '0.0532', '-0.1277', '0.05493', '0.14', '-0.04367', '-0.0715', '-0.08417', '-0.0625', '0.04935', '0.0231', '-0.1759', '-0.11884', '-0.122', '-0.10614', '-0.04022', '-0.2109', '0.10004', '-0.004456', '0.253', '-0.0313', '-0.004246', '-0.05112', '0.02623', '0.10596', '0.1406', '-0.1062', '0.06995', '0.01778', '0.2158', '0.09216', '0.07806', '-0.1362', '-0.001818', '-0.0217', '-0.0567', '-0.1143', '0.0525', '-0.05453', '0.0869', '-0.0564', '-0.0632', '-0.1072', '-0.06366', '0.1757', '-0.0494', '0.059', '-0.05392', '-0.0215', '0.06158', '-0.02074', '-0.1428', '-0.08624', '0.02965', '-0.07', '-0.11884', '0.05585', '0.10724', '0.1147', '-0.02635', '0.0354', '0.046', '-0.02562', '0.2485', '0.1633', '-0.1752', '0.1482', '-0.064', '0.03888', '0.01162', '-0.05392', '-0.02853', '0.0789', '0.08374', '-0.1692', '-0.12024', '-0.0597', '-0.04388', '0.02272', '0.042', '0.09686', '-0.051', '0.007195', '0.0871', '0.0808', '0.09015', '-0.02457', '0.09296', '0.11176', '0.06647', '-0.01941', '0.3293', '0.10266', '0.2537', '-0.133', '-0.03848', '0.00832']",,,,,,,
mondo:0015010,atypical glycine encephalopathy,"['Glycine encephalopathy with normal serum Glycine', 'atypical non-ketotic hyperglycinemia', 'GLYCINE encephalopathy with normal serum GLYCINE', 'atypical NKA']",,617301,289863,C4310943,"['0.05423', '0.3335', '-0.5015', '0.09235', '-0.2815', '-0.665', '-0.1295', '0.3103', '-0.2161', '0.2896', '-0.435', '-0.2664', '-0.2659', '0.314', '0.5874', '-0.2451', '-0.3452', '-0.3274', '0.12134', '-0.774', '0.1515', '-0.1731', '0.3743', '0.059', '0.003815', '-0.1065', '-0.288', '-0.289', '-0.1715', '0.1014', '0.3906', '0.1215', '0.5474', '0.522', '0.1234', '-0.06235', '-0.774', '-0.497', '-0.1886', '0.1296', '0.0996', '-0.7847', '0.10425', '-0.002821', '0.1826', '-0.0449', '-0.4976', '0.0941', '-0.589', '0.5225', '0.1305', '0.57', '-0.6494', '-0.1522', '-0.1896', '-0.2491', '0.3574', '-0.2157', '-0.2524', '0.5405', '0.1315', '-0.1001', '0.594', '0.1798', '-0.1438', '0.3418', '0.3677', '0.5317', '-0.04938', '0.4468', '-0.333', '0.08563', '0.1808', '0.3215', '0.3726', '0.5757', '0.3232', '-0.1991', '-0.02396', '0.1927', '0.00876', '0.2664', '-0.4836', '0.1285', '0.5635', '0.1411', '0.3044', '0.06464', '0.654', '0.1978', '0.771', '0.3574', '0.00929', '0.2311', '0.3672', '0.4802', '0.4016', '-0.02913', '0.2786', '-0.01857']",,,,,,,
mondo:0015011,optic atrophy 11,"['OPA11', 'optic atrophy 11', 'YME1L1 autosomal recessive isolated optic atrophy', 'optic atrophy type 11', 'autosomal recessive isolated optic atrophy caused by mutation in YME1L1']",0111436,617302,,CN230145,,,,,,,,
mondo:0015012,mucopolysaccharidosis-like syndrome with congenital heart defects and hematopoietic disorders,"['mucopolysaccharidosis-like plus disease', 'MPSPS', 'mucopolysaccharidosis-plus syndrome']",,617303,505248,C4310627,,,,,,,,
mondo:0015013,retinitis pigmentosa 77,"['RP77', 'REEP6 retinitis pigmentosa', 'retinitis pigmentosa 77', 'retinitis pigmentosa type 77', 'retinitis pigmentosa caused by mutation in REEP6']",0080350,617304,,C4310626,,,,,,,,
mondo:0015014,"coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness","['coloboma, osteopetrosis, microphthalmia, macrocephaly, albinism, and deafness', 'COMMAD', 'COMMAD syndrome']",,617306,603494,C4310625,"['-0.05902', '0.0912', '0.08673', '-0.0849', '0.1023', '-0.0918', '-0.01041', '0.1636', '-0.03696', '-0.006294', '-0.03735', '-0.0957', '-0.01366', '-0.0478', '-0.10614', '-0.0636', '0.1268', '-0.0756', '0.04865', '-0.2595', '-0.01101', '-0.05704', '0.112', '-0.05786', '0.05353', '0.04312', '-0.0755', '-0.00912', '0.0407', '-0.04355', '0.0592', '0.007446', '0.1638', '0.0587', '0.0481', '-0.02129', '-0.06635', '-0.1406', '-0.10693', '-0.1702', '0.0951', '-0.09656', '0.053', '-0.1059', '-0.02234', '-0.1727', '0.02895', '0.1251', '0.05307', '-0.06128', '-0.04684', '0.00351', '0.002218', '-0.034', '-0.04605', '-0.07416', '0.08405', '-0.0636', '-0.142', '0.00742', '0.0353', '-0.009995', '0.04855', '0.10876', '-0.0428', '-0.02022', '0.1299', '0.118', '-0.12335', '0.1884', '-0.12085', '0.04517', '0.006252', '-0.1035', '0.0449', '-0.06635', '0.07983', '-0.1278', '-0.04926', '-0.0642', '0.04767', '0.001038', '-0.07935', '0.2318', '-0.0805', '-0.065', '-0.008095', '0.2096', '0.0727', '0.05035', '0.0506', '0.1919', '0.05554', '0.03555', '0.2642', '-0.02946', '0.1522', '-0.1163', '0.0727', '0.0601']",,,,,,,
mondo:0015015,congenital bile acid synthesis defect 6,"['CBAS6', 'congenital bile acid synthesis defect caused by mutation in ACOX2', 'bile acid synthesis defect, congenital, type 6', 'bile acid synthesis defect, congenital, 6', 'congenital bile acid synthesis defect type 6', 'ACOX2 congenital bile acid synthesis defect']",0111067,617308,,C4310624,,,,,,,,
mondo:0015016,anterior segment dysgenesis 6,"['anterior segment dysgenesis type 6', 'anterior segment dysgenesis 6', 'anterior segment dysgenesis 6, multiple subtypes', 'ASGD6']",0080611,617315,,C4310623,,,,,,,,
mondo:0015017,anterior segment dysgenesis 8,"['ASGD8', 'anterior segment dysgenesis 8', 'anterior segment dysgenesis caused by mutation in CPAMD8', 'CPAMD8-related anterior segment dysgenesis', 'CPAMD8 anterior segment dysgenesis', 'anterior segment dysgenesis type 8']",0080613,617319,519388,C4310622,,,,,,,,
mondo:0015018,"ichthyosis, congenital, autosomal recessive 12","['ichthyosis, congenital, autosomal recessive type 12', 'ichthyosis, congenital, autosomal recessive 12', 'ARCI12']",,617320,,C4310621,,,,,,,,
mondo:0015019,Yao syndrome,"['YAOS', 'Yao syndrome']",,617321,,C4310620,,,,,,,,
mondo:0015020,"intellectual disability, autosomal recessive 59","['IMPA1 autosomal recessive non-syndromic intellectual disability', 'intellectual disability, autosomal recessive type 59', 'MRT59', 'mental retardation, autosomal recessive 59', 'autosomal recessive non-syndromic intellectual disability caused by mutation in IMPA1', 'mental retardation, autosomal recessive type 59', 'intellectual disability, autosomal recessive 59']",0081221,617323,,C4310619,,,,,,,,
mondo:0015021,"hypotonia, ataxia, and delayed development syndrome","['HADDS', 'hypotonia, ataxia, and delayed development syndrome']",0081176,617330,,C4310618,,,,,,,,
mondo:0015022,intellectual developmental disorder with dysmorphic facies and ptosis,"['IDDDFP', 'intellectual developmental disorder with dysmorphic facies and ptosis']",,617333,,C4310617,"['-0.10626', '0.11096', '0.07086', '-0.1415', '0.0263', '-0.1558', '0.0314', '0.2308', '-0.2089', '-0.0772', '-0.04993', '-0.02177', '0.05103', '-0.03076', '-0.089', '-0.001705', '0.039', '-0.04697', '-0.131', '-0.3032', '0.002663', '0.00477', '0.1266', '-0.03537', '0.06012', '-0.0304', '-0.0541', '-0.02637', '0.05206', '-0.0917', '0.10254', '-0.01978', '0.2251', '0.10956', '0.04367', '-0.02782', '-0.0713', '-0.1062', '-0.0429', '-0.1571', '0.1071', '-0.1328', '0.00828', '0.02924', '-0.01692', '-0.1372', '0.003956', '0.1608', '-0.05527', '0.01717', '-0.1333', '0.0641', '-0.0176', '-0.02094', '-0.01276', '-0.06204', '0.05316', '-0.0927', '-0.1259', '0.0656', '0.0733', '0.000408', '0.002598', '0.0631', '0.00989', '-0.01324', '0.12427', '0.1989', '-0.1455', '0.1953', '-0.1749', '0.0637', '0.10187', '-0.0547', '-0.01337', '0.06866', '0.11884', '-0.0997', '-0.1466', '-0.0685', '0.0959', '-0.02438', '-0.0588', '0.2434', '0.0101', '0.0605', '-0.02873', '0.1504', '0.1985', '0.08234', '0.07825', '0.186', '0.0341', '0.0635', '0.2683', '0.06757', '0.1283', '-0.1439', '0.1333', '0.1282']",,0009070,,,,,
mondo:0015023,MYPN-related myopathy,"['NEM11', 'nemaline myopathy type 11', 'nemaline myopathy 11', 'nemaline myopathy caused by mutation in MYPN', 'nemaline myopathy 11, autosomal recessive', 'MYPN nemaline myopathy']",0110933,617336,,CN240509,,,,,,,,
mondo:0015024,"ectodermal dysplasia 12, hypohidrotic/hair/tooth/nail type","['ectodermal dysplasia syndrome caused by mutation in KDF1', 'KDF1 ectodermal dysplasia syndrome', 'ectodermal dysplasia 12, hypohidrotic/hair/Tooth/nail type', 'ECTD12']",0111652,617337,,C4310616,,,,,,,,
mondo:0015025,"developmental and epileptic encephalopathy, 51","['early infantile epileptic encephalopathy caused by mutation in MDH2', 'MDH2 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, type 51', 'developmental and epileptic encephalopathy 51', 'DEE51', 'epileptic encephalopathy, early infantile, 51', 'EIEE51']",0080433,617339,,CN240510,,,,,,,,
mondo:0015026,cerebroretinal microangiopathy with calcifications and cysts 2,"['CRMCC2', 'cerebroretinal microangiopathy with calcifications and cysts 2', 'Coats plus syndrome caused by mutation in STN1', 'cerebroretinal microangiopathy with calcifications and cysts type 2', 'STN1 Coats plus syndrome']",,617341,,CN240513,,,,,,,,
mondo:0015027,familial isolated hyperparathyroidism,"['familial isolated hyperparathyroidism', 'FIHPT', 'FIHP']",,,99879,CN207422,"['0.495', '-0.4822', '-0.3901', '0.2153', '-0.2081', '0.942', '-0.521', '0.444', '-0.5103', '0.03607', '0.11017', '-0.152', '-0.514', '0.479', '-0.2678', '-0.02388', '-0.354', '0.0916', '-0.854', '-1.127', '-0.06854', '-0.6724', '0.3289', '-0.28', '0.5737', '-0.07587', '-0.2157', '-0.728', '0.31', '-0.008766', '0.8994', '0.2979', '0.1603', '0.0674', '-0.898', '-0.6333', '-0.0243', '0.146', '0.527', '0.263', '0.3352', '-0.439', '0.3892', '-0.736', '0.7803', '-0.5376', '-0.05228', '-0.04868', '0.579', '0.0703', '0.1282', '0.2803', '0.6714', '0.093', '-0.774', '-0.0577', '-0.448', '0.02495', '-0.748', '0.0495', '0.5635', '-0.03354', '-0.2507', '-0.253', '-0.5317', '0.6', '0.006275', '0.8433', '-0.358', '0.07306', '0.416', '0.2094', '0.889', '-0.2122', '-0.0781', '0.1348', '0.1256', '0.8374', '0.65', '0.5117', '-0.1304', '0.1208', '0.02974', '0.04675', '-0.1244', '-0.2703', '0.07184', '-0.1968', '1.085', '0.5156', '-0.03577', '0.3113', '-0.3677', '-0.6875', '0.9487', '-0.05728', '-0.1528', '-0.553', '-0.1776', '0.2102']",C94830,,,,,,
mondo:0015028,"48,XXYY syndrome","['48,XXYY variant of Klinefelter^s syndrome', 'XXYY syndrome', '48,XXYY Klinefelter syndrome', '48, XXYY syndrome']",,,10,C2936741,,C89801,,,758.81,,10048230,
mondo:0015029,reticular perineurioma,,,,100000,CN197319,,,,,,,,
mondo:0015030,sclerosing perineurioma,,,,100001,CN197320,,,,,,,,
mondo:0015031,extraneural perineurioma,['soft tissue perineurioma'],,,100002,CN197321,,,,,,,,
mondo:0015032,intraneural perineurioma,"['intraneural perineurioma', 'intraneural perineurioma (WHO grade I)']",4696,,100003,C1370658,,C6911,,,,,,
mondo:0015033,"ABeta amyloidosis, dutch type","['hereditary cerebral hemorrhage with amyloidosis, Dutch type', 'HCHWA, Dutch type', 'hereditary cerebral haemorrhage with amyloidosis, Dutch type', 'HCHWA-D', 'ABetaE22Q amyloidosis', 'cerebral amyloid angiopathy, APP-related, Dutch variant']",,,100006,,"['0.527', '-0.5825', '-0.9487', '0.1948', '0.00635', '-0.3313', '-0.4497', '0.44', '-1.151', '0.1818', '-0.2954', '-0.04953', '-0.504', '-0.08905', '-0.516', '-0.3833', '-0.1707', '-0.639', '-0.0576', '-0.4192', '0.3079', '-0.0773', '0.602', '-0.1081', '-0.2147', '0.1914', '-0.6777', '0.03702', '0.497', '0.306', '0.0955', '-0.4922', '1.254', '-0.4504', '0.3232', '-0.7065', '-0.3325', '0.2634', '0.04895', '0.08167', '0.3872', '-0.4612', '0.05536', '0.2103', '0.64', '-0.1188', '-0.7036', '0.209', '0.1844', '0.862', '0.3748', '0.7075', '0.3584', '-0.504', '-0.4036', '0.2913', '0.359', '0.1543', '-0.1321', '-0.761', '-0.673', '0.29', '0.3923', '-0.8154', '0.21', '-0.11755', '-0.02675', '0.8857', '-1.035', '0.463', '0.03635', '0.2349', '-0.2229', '0.1354', '0.638', '0.7407', '-0.3662', '1.047', '-0.4634', '-0.6323', '-0.3596', '-0.4211', '-0.01024', '0.07635', '0.297', '-0.4106', '-0.04453', '-0.0558', '0.07153', '-0.08057', '0.573', '-0.2502', '-0.599', '-0.10046', '0.3728', '0.507', '-0.4365', '-0.3516', '0.195', '0.1534']",,,,277.39,,,
mondo:0015034,lissencephaly with cerebellar hypoplasia type A,,,,100011,CN228900,,,,,,,,
mondo:0015035,lissencephaly with cerebellar hypoplasia type B,,,,100012,CN228901,,,,,,,,
mondo:0015036,lissencephaly with cerebellar hypoplasia type C,,,,100013,CN228902,,,,,,,,
mondo:0015037,lissencephaly with cerebellar hypoplasia type D,,,,100014,CN228903,,,,,,,,
mondo:0015038,lissencephaly with cerebellar hypoplasia type E,,,,100015,CN228904,,,,,,,,
mondo:0015039,lissencephaly with cerebellar hypoplasia type F,,,,100016,CN228905,,,,,,,,
mondo:0015040,myelodysplastic syndrome with excess blasts-1,"['refractory anaemia with excess blasts type 1', 'refractory anemia with excess blasts type 1', 'RAEB-1', 'RAEB-I', 'myelodysplastic syndrome with Excess blasts-1', 'MDS-EB-1']",,,100019,C1318550,,C7167,,,,,,
mondo:0015041,myelodysplastic syndrome with excess blasts-2,"['refractory anemia with excess blasts type 2', 'refractory anaemia with excess blasts type 2', 'RAEB-2', 'myelodysplastic syndrome with Excess blasts-2', 'MDS-EB-2', 'RAEB-II']",,,100020,C1318551,,C7168,,,,,,
mondo:0015042,primary plasmacytoma of the bone,,,,100021,CN197327,,,,,,,,
mondo:0015043,extramedullary soft tissue plasmacytoma,,,,100022,CN197328,,,,,,C90.2,,
mondo:0015044,mu-heavy chain disease,"['mu heavy chain disease', 'mu-HCD', 'mu chain disease']",0060128,,100024,,,C3892,,,273.2,,,
mondo:0015045,alpha-heavy chain disease,"['Immunoproliferative small intestinal disease', 'Mediterraneanl lymphoma', 'Mediterranean lymphoma', 'IPSID', 'Seligmann^s disease', 'Mediterranean abdominal lymphoma', 'Alpha-HCD', 'Alpha heavy chain disease', 'alpha chain disease']",0060126,,100025,C0021071,,C3132,1001798,D007161,,,,
mondo:0015046,gamma-heavy chain disease,"['Franklin disease', 'gamma-HCD', 'Franklin^s disease', 'gamma heavy chain disease']",0060127,,100026,,,C3083,,,273.2,,,
mondo:0015047,amelogenesis imperfecta type 1,['hypoplastic amelogenesis imperfecta'],,,100031,,"['-0.04657', '0.0485', '0.1045', '-0.0609', '0.08203', '-0.0671', '0.003983', '0.1395', '-0.0766', '-0.07635', '-0.0757', '-0.0515', '-0.04333', '-0.02115', '-0.03128', '-0.06573', '0.02615', '-0.03912', '-0.02144', '-0.182', '0.00526', '-0.02438', '0.1409', '-0.05612', '0.03635', '0.0152', '-0.04022', '-0.01913', '0.04224', '-0.0614', '0.02448', '0.01588', '0.05984', '0.07745', '0.1012', '-0.0628', '-0.005363', '-0.09766', '-0.01965', '-0.1357', '0.0197', '-0.1014', '0.0258', '-0.0762', '-0.06836', '-0.06177', '0.002626', '0.12305', '0.02643', '0.01216', '0.0616', '-0.0435', '0.0778', '-0.0421', '-0.09424', '-0.0712', '0.04062', '-0.09845', '-0.11005', '0.04822', '0.0648', '0.04172', '-0.01839', '-0.02798', '0.001282', '-0.0273', '0.08276', '0.0865', '-0.08264', '0.0903', '-0.0813', '0.02914', '0.04907', '-0.0872', '0.03105', '0.02771', '-0.006607', '-0.02885', '-0.0745', '-0.0769', '0.004295', '0.03857', '-0.03952', '0.0907', '-0.02534', '0.01174', '-0.0308', '0.1102', '0.1451', '-0.02272', '-0.02185', '0.10376', '0.02507', '0.08716', '0.185', '0.011116', '0.1047', '-0.1388', '0.02882', '0.03262']",,,,520.5,,,
mondo:0015048,amelogenesis imperfecta type 2,"['hypomaturation amelogenesis imperfecta', 'amelogenesis imperfecta hypomaturation type']",,,100033,,"['-0.012314', '0.0743', '0.0682', '-0.007774', '0.03577', '-0.03867', '0.02136', '0.0775', '-0.012825', '-0.02411', '-0.04218', '-0.03093', '-0.04266', '-0.03577', '0.02089', '-0.06433', '0.02362', '-0.04456', '-0.006924', '-0.12415', '0.011406', '-0.01552', '0.0918', '-0.03598', '0.035', '0.02544', '-0.035', '-0.013405', '0.00578', '-0.03433', '-0.00806', '0.03574', '0.0588', '0.04587', '0.07294', '-0.0357', '0.01237', '-0.0679', '-0.04315', '-0.12067', '0.0006776', '-0.1043', '0.01877', '-0.05817', '-0.04037', '-0.03543', '0.004333', '0.11523', '0.05255', '0.0196', '0.05743', '-0.0579', '0.0573', '-0.000939', '-0.05344', '-0.067', '0.0594', '-0.0756', '-0.079', '0.03854', '0.05914', '0.02356', '0.01343', '-0.02072', '-0.00228', '0.00279', '0.0775', '0.05222', '-0.07214', '0.0669', '-0.0662', '-0.00615', '0.014824', '-0.08026', '0.05267', '0.01833', '0.007175', '-0.02197', '-0.04773', '-0.0693', '-0.006542', '0.02309', '-0.03864', '0.0793', '-0.0457', '-0.003157', '0.005108', '0.0762', '0.12115', '-0.004726', '-0.002924', '0.06976', '0.002047', '0.0458', '0.1409', '0.0203', '0.0747', '-0.0965', '0.04022', '0.005333']",,,C536606,520.5,,,
mondo:0015049,solitary necrotic nodule of the liver,['hepatic solitary necrotic nodule'],,,100035,CN197336,,,,,,,,
mondo:0015050,esophageal duplication cyst,,,,100047,,,,,,,,,
mondo:0015051,tubular duplication of the esophagus,,,,100048,,,,,,,,,
mondo:0015053,hereditary angioedema type 1,"['hereditary angioneurotic edema type 1', 'HAE 1', 'hereditary angioneurotic oedema type 1', 'HAE-I']",,,100050,,"['0.2439', '0.6885', '-0.7935', '0.1859', '-0.4136', '0.3652', '0.8145', '-0.5684', '-0.04007', '-0.3691', '-0.454', '0.524', '0.0816', '0.2142', '-0.0771', '0.11053', '-0.3743', '-0.1514', '-0.4673', '-0.592', '-0.0664', '-0.295', '1.311', '-0.2196', '-0.11707', '0.2253', '0.114', '-0.388', '-0.0825', '-0.639', '0.124', '0.992', '0.367', '0.4136', '-0.0821', '0.2622', '-0.1664', '0.116', '-0.4556', '0.454', '0.3755', '0.1418', '0.12305', '0.03085', '0.3135', '-0.1131', '0.1219', '0.0971', '0.562', '0.6206', '-0.02647', '-0.2184', '0.281', '-0.3606', '-0.2969', '0.1934', '0.6553', '-0.339', '0.1533', '0.2935', '-0.2085', '0.4546', '0.1128', '-0.003332', '0.322', '0.2944', '0.368', '0.2961', '0.005306', '0.548', '-0.754', '-0.11993', '-0.010666', '-0.4534', '0.637', '0.3481', '0.2274', '0.2192', '-0.614', '-0.433', '0.0775', '-0.2319', '0.6343', '0.4028', '0.01391', '0.1467', '0.401', '-0.08844', '-0.03796', '-0.1234', '0.3545', '0.08887', '0.5547', '0.09467', '0.6567', '0.512', '0.2463', '-0.8457', '-0.541', '0.3062']",,,,279.8,,,
mondo:0015054,hereditary angioedema type 2,"['HAE 2', 'HAE-II', 'hereditary angioneurotic edema type 2', 'hereditary angioneurotic oedema type 2']",,,100051,C1862892,"['0.744', '0.03925', '-0.338', '-0.3462', '-0.2291', '0.01619', '0.2416', '-0.06235', '-0.4253', '0.1054', '-0.3506', '0.718', '0.2233', '0.2737', '-0.1613', '-0.00199', '-0.01974', '-0.1857', '-0.1226', '-0.0586', '0.11536', '-0.3022', '1.233', '-0.1114', '-0.3494', '0.242', '0.0489', '-0.4446', '-0.0876', '-0.4448', '0.0338', '0.7085', '0.5317', '-0.07367', '-0.08276', '-0.008286', '-0.1583', '0.1383', '-0.11255', '0.153', '0.4885', '-0.0726', '0.1498', '0.0699', '0.3115', '0.1131', '0.0849', '0.0743', '0.1947', '0.3696', '0.05127', '-0.43', '0.2148', '-0.4753', '-0.352', '0.558', '0.783', '-0.8335', '-0.3674', '-0.2362', '-0.2664', '0.6084', '0.1501', '-0.2915', '0.394', '0.299', '0.1749', '0.3884', '-0.3809', '0.4607', '-0.00796', '-0.02597', '0.0896', '-0.5957', '0.4824', '0.2104', '0.157', '0.2808', '-0.52', '-0.2996', '-0.201', '-0.2908', '0.1603', '0.04233', '-0.1306', '0.3552', '0.241', '0.3044', '0.4153', '-0.2104', '0.3552', '0.1371', '0.4878', '0.2189', '0.7734', '0.0671', '0.388', '-0.3538', '-0.834', '0.2786']",,,,,,,
mondo:0015055,acquired angioedema type 2,"['acquired angioneurotic oedema type 2', 'acquired angioneurotic edema type 2', 'AAE II', 'AAE 2']",,,100055,CN197347,,,,,,,,
mondo:0015056,acquired angioedema type 1,"['acquired angioneurotic oedema type 1', 'acquired angioneurotic edema type 1']",,,100056,CN197348,,,,,,,,
mondo:0015057,renin-angiotensin-aldosterone system-blocker-induced angioedema,"['Raas-blocker-induced angioneurotic edema', 'angioedema induced by ACE inhibitors, susceptibility to', 'AEACEI', 'RAE', 'susceptibility to angioedema induced by ace inhibitors', 'Raas-blocker-induced angioneurotic oedema', 'reactive angioendotheliomatosis', 'renin-angiotensin-aldosterone system-blocker-induced angioneurotic edema', 'Raas-blocker-induced angioedema', 'renin-angiotensin-aldosterone system-blocker-induced angioneurotic oedema']",,,100057,C1304495,,,,C535293,,,,
mondo:0015059,progressive non-fluent aphasia,"['non-fluent variant PPA', 'non-fluent primary progressive aphasia', 'Agramatic variant of primary progressive aphasia', 'Primary Progressive Nonfluent aphasia', 'Agramatic variant of PPA']",,,100070,,"['-0.1759', '0.297', '0.2922', '0.2347', '-0.7036', '0.1769', '0.301', '-0.01352', '-0.623', '-0.661', '0.5947', '0.01434', '0.02525', '0.04276', '0.2058', '-0.7197', '-0.3', '-0.538', '-0.1519', '-0.7993', '-0.277', '0.537', '-0.4912', '0.1517', '0.639', '0.2073', '-0.1848', '-0.7144', '-0.4636', '0.3584', '-0.0874', '0.25', '0.702', '0.278', '-0.1076', '0.1406', '0.09827', '-0.01715', '-0.1578', '-0.9424', '0.999', '-1.132', '0.01374', '0.07715', '0.5645', '0.4968', '-0.742', '-0.2444', '-0.02048', '0.10974', '0.55', '0.4246', '-0.01717', '0.11127', '0.476', '0.534', '-0.739', '0.4482', '0.01322', '0.3047', '-0.5576', '0.331', '0.2471', '-0.0823', '-0.4875', '0.1222', '-0.0734', '0.4766', '-0.739', '0.5645', '0.03687', '-0.504', '0.03262', '-0.717', '-0.05338', '0.2008', '0.2313', '0.867', '-0.1558', '-0.06555', '-0.02242', '-0.2275', '-0.3877', '0.653', '-0.09894', '-0.02202', '0.03976', '-0.0913', '0.7373', '-0.00491', '-0.3188', '0.4998', '-0.145', '0.927', '0.9146', '0.6265', '0.086', '-0.06287', '0.10596', '0.3782']",C85025,,D057178,,,10029542,
mondo:0015060,mosaic trisomy 3,"['trisomy 3 mosaicism', 'Mosaic trisomy chromosome 3', 'Mosaic trisomy type 3']",,,100071,CN073992,,,,,,,,
mondo:0015061,neurogenic thoracic outlet syndrome,"['neurogenic TOS', 'neurogenic costoclavicular syndrome', 'neurogenic thoracic outlet compression syndrome', 'NTOS', 'neurogenic cervical rib syndrome']",,,100073,C0751549,,,,,,,,
mondo:0015062,"gastric neuroendocrine tumor, well differentiated, low or intermediate grade","['gastric well differentiated endocrine tumor', 'gastric well differentiated endocrine tumour', 'well-differentiated neuroendocrine tumours of the stomach', 'well-differentiated neuroendocrine tumors of the stomach', 'gastric well differentiated endocrine tumor/carcinoma', 'gastric neuroendocrine tumour', 'GNET', 'gastric NET G1/2', 'gastric neuroendocrine tumor', 'gastric NET']",,,,CN197355,,C95871,,,,,,
mondo:0044305,"ectodermal dysplasia 13, hair/tooth type","['ectodermal dysplasia 13, hair/tooth type', 'ECTD13']",0111650,617392,,C4479322,,,,,,,,
mondo:0044306,"neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination","['neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination', 'severe neurodevelopmental disorder with feeding difficulties-stereotypic hand movement-bilateral cataract', 'NECFM']",,617393,500545,C4479333,"['-0.0962', '0.1227', '0.0833', '-0.1344', '0.05127', '-0.1821', '0.01805', '0.3123', '-0.2744', '-0.03763', '-0.1478', '-0.1587', '-0.0004156', '-0.02489', '0.03937', '-0.06635', '0.07007', '-0.08264', '-0.1964', '-0.3135', '0.0358', '-0.0797', '0.03564', '-0.03107', '0.02214', '-0.1373', '0.006996', '0.02965', '0.04657', '-0.142', '0.02646', '-0.000672', '0.2288', '0.06366', '-0.03406', '0.064', '-0.0096', '-0.0729', '-0.0951', '-0.14', '0.1346', '-0.1004', '0.02931', '0.0905', '-0.04745', '-0.1456', '-0.02101', '0.119', '-0.0646', '0.1534', '-0.0651', '0.0941', '-0.0906', '0.01613', '-0.04922', '0.05234', '0.1092', '-0.01464', '-0.12067', '0.1059', '0.0889', '0.066', '0.075', '0.04135', '-0.01607', '0.03397', '0.1986', '0.1494', '-0.129', '0.2017', '-0.1284', '0.1462', '0.02107', '-0.0967', '0.00539', '0.02834', '0.1218', '-0.1327', '-0.10315', '-0.02254', '0.02675', '0.00562', '-0.0598', '0.27', '-0.0268', '0.1035', '0.02284', '0.11597', '0.2424', '0.05194', '0.006638', '0.1956', '0.002968', '0.0654', '0.1947', '0.1472', '0.1366', '-0.05655', '0.09827', '0.09625']",,,,,,,
mondo:0044308,bardet-biedl syndrome 21,"['Bardet-Biedl syndrome 21', 'BBS21']",0081010,617406,,C4319932,,,,,,,,
mondo:0044309,Diamond-Blackfan anemia 16,"['DBA16', 'Diamond-Blackfan anemia 16']",0111893,617408,,C4479424,,,,,,,,
mondo:0044310,Diamond-Blackfan anemia 17,"['Diamond-Blackfan anemia 17', 'DBA17']",0111880,617409,,C4479428,,,,,,,,
mondo:0044311,"brachycephaly, trichomegaly, and developmental delay","['Macinnes syndrome', 'brachycephaly, trichomegaly, and developmental delay', 'BTDD']",0070415,617412,,C4479431,,,,,,,,
mondo:0044312,immunoskeletal dysplasia with neurodevelopmental abnormalities,"['ISDNA', 'IMMUNOSKELETAL dysplasia with neurodevelopmental abnormalities']",,617425,,C4479452,"['-0.02473', '0.014595', '0.0126', '-0.02011', '0.016', '-0.02481', '0.01301', '0.04126', '-0.02277', '-0.02744', '-0.01595', '-0.005085', '0.002117', '0.01155', '-0.00961', '-0.01761', '-0.000539', '-0.013145', '-0.01912', '-0.067', '0.0002575', '-0.003572', '0.02962', '-0.00585', '0.00867', '-0.02158', '-0.006725', '-0.0004973', '0.01653', '-0.01366', '0.02316', '-0.011345', '0.03305', '0.00579', '0.01446', '-0.00584', '-0.02132', '-0.02487', '-0.00683', '-0.02138', '0.0173', '-0.01707', '0.01648', '-0.011185', '-0.003107', '-0.0343', '-0.01787', '0.02168', '0.006413', '0.00118', '-0.001609', '0.00122', '0.00746', '0.001492', '-0.0215', '-0.011505', '0.02158', '-0.01942', '-0.0378', '0.01889', '0.01884', '0.00439', '0.002684', '0.007084', '-0.00997', '-0.005447', '0.03024', '0.0171', '-0.02579', '0.0377', '-0.02896', '0.00424', '-0.00848', '-0.00878', '0.01147', '0.01348', '0.01859', '-0.003176', '-0.02312', '-0.01338', '-0.00468', '0.0009394', '-0.002861', '0.04037', '-0.01608', '0.007298', '0.01587', '0.03004', '0.04352', '0.02612', '0.01', '0.02145', '0.002117', '0.01072', '0.0682', '0.0228', '0.0338', '-0.04364', '0.01446', '0.00837']",,,,,,,
mondo:0044313,"intellectual disability, autosomal recessive 60","['mental retardation, autosomal recessive 60', 'intellectual disability, autosomal recessive 60', 'MRT60']",0081222,617432,,,,,,,,,,
mondo:0044314,retinitis pigmentosa 78,"['retinitis pigmentosa 78', 'RP78']",,617433,,C4479481,,,,,,,,
mondo:0044315,craniosynostosis 7,"['CRS7', 'Crs7, digenic', 'craniosynostosis 7', 'craniosynostosis 7, susceptibility to', 'craniosynostosis 7, digenic']",,617439,,C4479496,,,,,,,,
mondo:0044316,"thrombocytopenia, anemia, and myelofibrosis","['thrombocytopenia, anemia, and myelofibrosis', 'THAMY']",,617441,,C4479504,,,,,,,,
mondo:0044317,premature ovarian failure 13,"['POF13', 'premature ovarian failure 13']",0080870,617442,,C4479510,,,,,,,,
mondo:0044318,intellectual developmental disorder with gastrointestinal difficulties and high pain threshold,"['Jansen de Vries syndrome', 'intellectual developmental disorder with gastrointestinal difficulties and high pain threshold', 'IDDGIP']",,617450,,C4479517,"['-0.04303', '0.04474', '0.01735', '-0.0381', '0.006496', '-0.0956', '0.02875', '0.1464', '-0.0842', '-0.0414', '-0.0397', '-0.02419', '0.01513', '0.0134', '-0.0661', '-0.0358', '-0.00678', '-0.02715', '-0.0543', '-0.1854', '-0.01226', '-0.02733', '0.0675', '-0.0359', '0.0353', '-0.013306', '-0.003193', '-0.01234', '-0.008736', '-0.04803', '0.04517', '-0.02216', '0.09595', '0.05374', '0.00637', '-0.014626', '-0.02293', '-0.02913', '-0.00888', '-0.0863', '0.01947', '-0.096', '0.02377', '-0.03009', '0.0093', '-0.0711', '-0.02153', '0.0469', '0.0226', '0.07556', '-0.0769', '0.01499', '0.004272', '0.0001303', '-0.03644', '0.01602', '0.05243', '-0.02364', '-0.1035', '0.006702', '0.04907', '0.06335', '0.001553', '0.0083', '-0.0042', '0.02913', '0.079', '0.0889', '-0.09656', '0.1033', '-0.06232', '0.03888', '0.002123', '-0.0641', '0.01994', '0.0647', '0.06354', '-0.00718', '-0.04324', '-0.04865', '-0.0284', '-0.00702', '-0.01762', '0.1025', '-0.001616', '0.04208', '0.0166', '0.0815', '0.12164', '0.03244', '0.0215', '0.0756', '-0.02803', '0.01869', '0.1614', '0.0521', '0.06976', '-0.0964', '-0.00964', '0.06464']",,,,,,,
mondo:0044319,"intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies","['intellectual developmental disorder with dysmorphic facies, seizures, and distal limb anomalies', 'IDDFSDA']",,617452,505237,C4479520,"['-0.05777', '0.06137', '0.0692', '-0.065', '0.03497', '-0.0975', '0.01084', '0.1377', '-0.11096', '-0.0677', '-0.03032', '-0.02031', '0.02019', '0.011116', '-0.03099', '-0.01718', '0.01566', '-0.05136', '-0.0699', '-0.1874', '0.01537', '-0.01689', '0.0721', '-0.01947', '0.05954', '-0.02428', '-0.02353', '-0.00164', '0.01958', '-0.06525', '0.07135', '-0.02066', '0.10345', '0.04218', '0.0262', '-0.02625', '-0.0321', '-0.0427', '-0.0446', '-0.0717', '0.05704', '-0.11926', '-0.00863', '-0.001743', '-0.003395', '-0.09265', '-0.02641', '0.0848', '-0.00976', '0.03323', '-0.065', '0.002176', '-0.00889', '-0.00783', '-0.03894', '-0.05853', '0.0431', '-0.04877', '-0.0975', '0.02106', '0.0471', '-0.003477', '0.001497', '0.02065', '-0.02238', '0.01312', '0.0956', '0.10223', '-0.097', '0.08636', '-0.0972', '0.03378', '0.04327', '-0.0486', '0.02417', '0.04578', '0.05673', '-0.03455', '-0.071', '-0.05353', '-0.00411', '0.00902', '-0.00873', '0.1289', '0.00487', '0.03464', '-0.01112', '0.09863', '0.12177', '0.01344', '0.0436', '0.1055', '0.00682', '0.0401', '0.1718', '0.03763', '0.0917', '-0.1056', '0.04675', '0.0614']",,,,,,,
mondo:0044320,retinitis pigmentosa 79,"['retinitis pigmentosa 79', 'RP79']",,617460,,C4479526,,,,,,,,
mondo:0044321,structural heart defects and renal anomalies syndrome,"['SHDRA', 'structural heart defects and renal anomalies syndrome']",,617478,,C4479549,,,,,,,,
mondo:0044322,intellectual developmental disorder with neuropsychiatric features,"['IDDNPF', 'intellectual developmental disorder with neuropsychiatric features']",,617532,,C4479636,"['-0.0783', '0.08264', '0.04712', '-0.08954', '0.0298', '-0.1384', '-0.001726', '0.181', '-0.1394', '-0.0403', '-0.05768', '-0.04385', '0.004887', '-0.00841', '-0.04385', '-0.01976', '-0.0002245', '-0.04807', '-0.0995', '-0.2532', '-0.02592', '-0.02565', '0.10974', '-0.04364', '0.054', '-0.0307', '-0.01897', '-0.02728', '0.00601', '-0.0847', '0.10583', '-0.02238', '0.2047', '0.0883', '0.00864', '-0.02724', '-0.0677', '-0.07916', '-0.04724', '-0.118', '0.0902', '-0.129', '0.008644', '-0.006752', '0.02219', '-0.1136', '-0.007603', '0.07605', '-0.006306', '0.0527', '-0.0799', '0.0394', '-0.00491', '0.001372', '-0.01576', '-0.02452', '0.07654', '-0.05215', '-0.11755', '0.02995', '0.0586', '0.04663', '0.009285', '0.02075', '-0.00193', '0.0478', '0.1019', '0.1451', '-0.133', '0.1273', '-0.1204', '0.003017', '0.0189', '-0.05234', '0.04572', '0.05637', '0.0745', '-0.04028', '-0.07465', '-0.0653', '0.0336', '-0.031', '-0.0425', '0.1753', '0.0001502', '0.03967', '0.01385', '0.1501', '0.1643', '0.05023', '0.0725', '0.1309', '-0.02647', '0.02695', '0.2319', '0.04822', '0.1104', '-0.12415', '0.07074', '0.0863']",,,,,,,
mondo:0044323,Rahman syndrome,"['RMNS', 'Rahman syndrome', 'autosomal dominant intellectual disability-craniofacial dysmorphism-macrocephaly-hypotonia syndrome due to H1-4 mutation']",,617537,642763,C4479637,,,,,,,,
mondo:0044324,Al Kaissi syndrome,"['Growth retardation, spine malformation, dysmorphic facies, and developmental delay', 'ALKAS', 'AL KAISSI syndrome']",,617694,,CN502749,"['0.01028', '0.01984', '-0.01202', '-0.00825', '0.002607', '-0.02335', '-0.005592', '0.02344', '-0.03427', '-0.01575', '-0.03128', '0.007442', '-0.00567', '0.02446', '-0.00858', '-0.02576', '-0.02138', '-0.002493', '-0.009834', '-0.0657', '-0.00633', '-0.0174', '0.02875', '0.008575', '0.0065', '0.003433', '-0.02054', '-0.01218', '-0.006184', '-0.01526', '0.04712', '-0.03363', '0.05338', '-0.01461', '0.02023', '-0.001564', '-0.006546', '-0.01114', '-0.000586', '-0.03992', '0.021', '-0.03026', '-0.00823', '-0.01348', '0.02228', '-0.04132', '0.0002344', '0.02495', '0.01956', '0.01582', '-0.01402', '-0.02379', '0.01947', '0.011795', '-0.02647', '-0.011', '0.012115', '-0.00919', '-0.03073', '0.001295', '0.02573', '-0.004402', '0.00793', '-0.006577', '0.01366', '-0.003805', '0.02817', '0.04', '-0.05362', '0.04205', '-0.05124', '0.00474', '-0.00232', '-0.003075', '0.01326', '0.02914', '-0.013596', '0.0214', '-0.008255', '-0.03156', '0.0001779', '-0.012764', '-0.0363', '0.0257', '-0.005447', '-0.02594', '0.02068', '0.02748', '0.0492', '0.005207', '-0.007458', '0.02908', '0.01421', '0.004726', '0.0985', '0.02826', '0.01915', '-0.05957', '0.004406', '0.02202']",,,,,,,
mondo:0044325,"Fanconi anemia, complementation group W","['FANCW', 'Fanconi anemia, complementation group W']",,617784,,CN653907,"['-0.02177', '0.133', '0.019', '-0.01353', '0.1395', '-0.1332', '-0.0784', '0.0912', '-0.0381', '-0.07367', '-0.03366', '0.0306', '0.004852', '0.02222', '-0.01246', '-0.0941', '-0.05695', '-0.06232', '-0.01224', '-0.1858', '0.04187', '-0.04788', '0.11426', '0.0146', '0.03806', '-0.0935', '-0.007034', '-0.05273', '-0.004475', '0.002277', '0.02591', '-0.02069', '0.1268', '0.11017', '0.04712', '-0.03143', '-0.1254', '-0.1284', '-0.10077', '-0.1307', '-0.02815', '-0.1355', '0.0612', '-0.0499', '-0.02985', '-0.1873', '-0.03738', '0.10754', '0.1079', '0.02063', '0.01582', '-0.03513', '0.03806', '0.0468', '0.001018', '-0.1065', '0.04953', '0.0491', '-0.203', '0.04285', '0.0921', '0.0206', '-0.001652', '-0.007786', '0.02496', '-0.02744', '0.10175', '0.1328', '-0.08704', '0.1404', '-0.0717', '-0.08325', '-0.01653', '-0.07574', '0.06476', '0.04092', '0.01291', '-0.0311', '-0.08563', '-0.0659', '0.03122', '-0.03622', '-0.03038', '0.03061', '-0.008766', '-0.00972', '0.05725', '0.1328', '0.158', '-0.03207', '0.1398', '0.04895', '0.01991', '-0.04788', '0.1959', '0.1848', '0.06995', '-0.1175', '-0.0018015', '0.08887']",,,,,,,
mondo:0044326,developmental delay and seizures with or without movement abnormalities,"['DEDSM', 'developmental delay and seizures with or without movement abnormalities']",0080473,617836,442835,CN769090,"['-0.0087', '0.03047', '0.008316', '-0.008354', '0.0008445', '-0.03778', '0.01553', '0.03708', '-0.02176', '-0.02167', '-0.01283', '-0.01153', '-0.001672', '0.008354', '-0.00169', '-0.01093', '-0.006626', '-0.02377', '-0.02214', '-0.04877', '-0.01258', '-0.010216', '0.01588', '-0.010345', '0.02292', '-0.00938', '-0.013306', '-0.00010735', '-0.002218', '-0.004173', '0.0226', '-0.001827', '0.02548', '0.005363', '0.00554', '-0.0002449', '-0.00783', '-0.008156', '-0.007328', '-0.03018', '0.00664', '-0.02786', '0.007664', '-0.00801', '0.003561', '-0.02266', '-0.005302', '0.014404', '0.00759', '0.01256', '-0.02177', '0.00397', '0.00699', '0.00994', '0.001146', '-0.01104', '0.01472', '-0.01563', '-0.04437', '0.003885', '0.01362', '0.004673', '0.003607', '0.0001785', '-0.003378', '0.00697', '0.02478', '0.01881', '-0.03323', '0.03784', '-0.01863', '0.01375', '0.006004', '-0.011955', '0.012146', '0.01567', '0.00957', '0.0008907', '-0.00803', '-0.01941', '0.01189', '-0.003145', '-0.006733', '0.02956', '0.005928', '0.01096', '-0.001918', '0.01965', '0.04718', '0.01886', '0.010025', '0.03056', '-0.00933', '0.004772', '0.04004', '0.0281', '0.01752', '-0.0387', '-0.00913', '0.011826']",,,,,,,
mondo:0044327,polycystic liver disease 4 with or without kidney cysts,"['polycystic liver disease 4 with or without kidney cysts', 'PCLD4']",,617875,,CN818987,"['0.01697', '0.11523', '0.01013', '-0.02802', '0.0562', '-0.1211', '-0.03903', '0.1418', '-0.0669', '-0.03915', '-0.0634', '-0.0388', '-0.01027', '0.0601', '-0.1332', '-0.1665', '-0.01604', '-0.03662', '-0.02098', '-0.2085', '0.02785', '-0.07385', '0.09814', '-0.0529', '0.03168', '-0.0876', '-0.007267', '-0.0009127', '0.06186', '-0.05597', '0.1414', '-0.05637', '0.1425', '-0.00925', '0.04016', '-0.10205', '-0.05847', '-0.05222', '0.00888', '-0.0592', '0.00892', '-0.07574', '0.074', '-0.02374', '-0.05112', '-0.11554', '-0.03824', '0.0705', '-0.02905', '0.04083', '-0.04114', '0.02325', '0.06525', '0.01662', '-0.04486', '-0.07294', '0.12024', '-0.0725', '-0.2249', '-0.03616', '0.1296', '0.08655', '0.001738', '0.00989', '-0.01854', '-0.05936', '0.1231', '0.1355', '-0.1133', '0.1219', '-0.04694', '-0.01554', '0.0587', '-0.09564', '0.04593', '0.02031', '-0.00689', '0.04654', '-0.11194', '-0.0561', '-0.04337', '0.010345', '-0.01591', '0.04327', '-0.04257', '-0.03836', '0.0862', '0.09314', '0.11584', '0.03964', '0.04404', '0.0891', '-0.01868', '0.0337', '0.2903', '0.04004', '0.0816', '-0.1738', '-0.05664', '0.0691']",,,,,,,
mondo:0044328,short-rib thoracic dysplasia 20 with polydactyly,"['short-rib thoracic dysplasia 20 with polydactyly', 'SRTD20']",,617925,,CN902090,,,,,,,,
mondo:0044329,"osteogenesis imperfecta, type 18","['OI18', 'osteogenesis imperfecta, type XVIII']",0111848,617952,,CN244563,,,,,,,,
mondo:0044330,hyperekplexia 4,"['hyperekplexia 4', 'HKPX4']",0080581,618011,,CN248518,,,,,,,,
mondo:0044332,childhood-onset benign chorea with striatal involvement,,,,494541,,,,,,,,,
mondo:0044333,alcohol-induced Wernicke-Korsakoff^s syndrome,"['alcoholic Korsakoff^s psychosis', 'alcohol-induced amnestic syndrome', 'alcohol-induced Wernicke-Korsakoff^s syndrome']",,,,,,C34366,,,,,,
mondo:0044334,connective and soft tissue neoplasm,"['neoplasm of skeletal and soft tissue', 'musculoskeletal and soft tissue tumor', 'tumour of soft tissue and bone', 'soft tissue and bone tumour', 'tumour of skeletal and soft tissue', 'connective and soft tissue tumor', 'tumor of skeletal and soft tissue', 'neoplasm of soft tissue and bone', 'musculoskeletal and soft tissue neoplasm', 'soft tissue and bone tumor', 'skeletal and soft tissue neoplasm', 'skeletal and soft tissue tumour', 'connective and soft tissue neoplasm', 'tumour of soft tissue and skeleton', 'neoplasm of soft tissue and skeleton', 'soft tissue and bone neoplasm', 'tumor of soft tissue and bone', 'tumor of soft tissue and skeleton', 'connective and soft tissue tumour', 'musculoskeletal and soft tissue tumour', 'skeletal and soft tissue tumor']",,,,,,C3810,,,,,,
mondo:0044335,benign soft tissue neoplasm,"['benign neoplasm of soft tissue', 'benign neoplasm of the soft tissue', 'benign soft tissue tumour', 'soft tissue neoplasm, benign', 'benign soft tissue neoplasm', 'benign tumor of soft tissue', 'benign soft tissue tumor', 'benign tumor of the soft tissue', 'benign tumour of soft tissue', 'benign tumour of the soft tissue']",,,,C0334450,,C4242,,,,,,
mondo:0044336,colorectal signet ring cell carcinoma,['colorectal signet Ring cell carcinoma'],,,,C1707440,,C43586,,,,,,
mondo:0044337,stromal sarcoma,"['stromal tumor, malignant', 'stromal sarcoma', 'stromal sarcoma, malignant']",,,,C1370723,,C6926,,,,,,
mondo:0044338,autoimmune primary ovarian failure,,,,,C0342508,,,,,279.49,,,
mondo:0044339,lumbar disk degenerative disorder,"['lumbar disk disease', 'degenerative disc disorder', 'degenerative disk disorder', 'lumbar disk degeneration, susceptibility to', 'lumbar Disc Degeneration', 'lumbar disc disease, susceptibility to', 'intervertebral disc disease, susceptibility to', 'lumbar disk herniation, susceptibility to', 'intervertebral disk degenerative disorder of lumbar region of vertebral column', 'IDD', 'degenerative disk disease', 'intervertebral disk disease', 'lumbar Disc degenerative disease', 'lumbar disk disease, susceptibility to', 'intervertebral disc disease', 'lumbar disc degeneration, susceptibility to', 'intervertebral DISC disease', 'degenerative disc disease', 'lumbar region of vertebral column intervertebral disc degenerative disorder', 'lumbar disc herniation, susceptibility to', 'intervertebral disc degenerative disorder of lumbar region of vertebral column', 'intervertebral disk disease, susceptibility to', 'degeneration of lumbar intervertebral disc', 'lumbar Disc degenerative disorder', 'lumbar region of vertebral column intervertebral disk degenerative disorder', 'lumbar disc disease']",,,,,"['-0.274', '0.1118', '0.106', '-0.04056', '0.0978', '-0.1396', '0.04315', '0.306', '-0.3508', '-0.10596', '-0.04996', '-0.06714', '-0.09015', '0.0773', '0.0316', '-0.0884', '-0.102', '-0.0726', '-0.1906', '-0.2998', '0.004757', '-0.00776', '0.2123', '0.01875', '0.01639', '0.1229', '0.0714', '-0.1282', '-0.0744', '0.02887', '-0.02678', '-0.185', '0.0731', '0.0818', '0.1625', '0.0314', '-0.02213', '-0.2354', '-0.0502', '-0.2018', '0.06198', '-0.1399', '-0.00874', '-0.0151', '0.06256', '-0.1776', '0.03915', '0.1475', '-0.01729', '-0.009674', '0.04565', '0.0626', '0.0858', '0.0789', '-0.1251', '-0.3047', '0.1743', '-0.0848', '-0.2019', '-0.0383', '0.2167', '0.001142', '-0.1406', '0.1558', '-0.22', '-0.011604', '0.2817', '0.3452', '-0.03613', '0.1427', '-0.1375', '0.06433', '0.037', '-0.1432', '-0.000613', '0.1865', '-0.00487', '0.1156', '-0.1976', '-0.1962', '-0.1775', '-0.04666', '-0.0567', '0.356', '-0.02293', '-0.10864', '0.1078', '0.02179', '0.1031', '0.004417', '-0.0572', '0.00879', '-0.0323', '0.0932', '0.2156', '-0.005367', '0.3542', '-0.1285', '-0.11597', '0.1395']",C27154,0004994,C535531,,,,
mondo:0044342,thoracic disk degenerative disorder,"['thoracic Disc Degeneration', 'thoracic region of vertebral column intervertebral disk degenerative disorder', 'thoracic Disc degenerative disease', 'intervertebral disk degenerative disorder of thoracic region of vertebral column', 'degeneration of thoracic intervertebral disc', 'thoracic Disc degenerative disorder', 'intervertebral disc degenerative disorder of thoracic region of vertebral column', 'thoracic region of vertebral column intervertebral disc degenerative disorder']",,,,C0263872,,C27155,,,,,,
mondo:0044343,cervical disk degenerative disorder,"['cervical Disc degenerative disorder', 'intervertebral disk degenerative disorder of cervical region of vertebral column', 'cervical region of vertebral column intervertebral disc degenerative disorder', 'cervical region of vertebral column intervertebral disk degenerative disorder', 'degeneration of cervical intervertebral disc', 'intervertebral disc degenerative disorder of cervical region of vertebral column', 'cervical Disc Degeneration', 'cervical Disc degenerative disease']",,,,C0410606,,C27156,,,,,,
mondo:0044344,Schistosoma japonicum infectious disease,"['Schistosoma japonicum caused disease or disorder', 'Schistosoma japonicum infection', 'schistosomiasis japonicum']",,,,,,C35001,,D012554,,,,
mondo:0044345,Schistosoma mansoni infectious disease,"['Schistosoma mansoni infection', 'Schistosoma mansoni caused disease or disorder']",,,,,,C35002,,D012555,,,,
mondo:0044346,echinococcus granulosus infectious disease,['Echinococcus granulosus caused disease or disorder'],,,,C0152068,,,,,122.4,,,
mondo:0044347,erythrocyte disorder,"['disease of erythrocyte', 'erythrocyte disease or disorder', 'disorder of erythrocyte', 'erythrocyte disease']",,,,C0221016,,,,,289.9,,,
mondo:0044348,hemoglobinopathy,"['haemoglobin disease', 'haemoglobin disorder']",,,,,,,,,282.7,,,
mondo:0044349,acquired hemoglobinopathy,['acquired hemoglobinopathy'],,,,C1263995,,,,,,,,
mondo:0044350,"hyperparathyroidism, primary, caused by water clear cell hyperplasia","['hyperparathyroidism, primary, caused by water clear cell hyperplasia']",,600166,,,,,,C563982,,,,
mondo:0044351,Schistosoma intercalatum infectious disease,"['Schistosoma intercalatum caused disease or disorder', 'infection by Schistosoma intercalatum']",,,,C0276932,,C35364,,,120.8,,,
mondo:0044355,isolated sternocostoclavicular hyperostosis,['isolated SCCH'],,,178311,C0020499,,,,,,,,
mondo:0044406,arthrogryposis-ectodermal dysplasia-other anomalies syndrome,['Stoll-Alembik-Finck syndrome'],,,3200,,,,,,,,,
mondo:0044617,X-linked keloid scarring-reduced joint mobility-increased optic cup-to-disc ratio syndrome,,,,482606,,,,,,,,,
mondo:0044619,propylthiouracil embryofetopathy,"['propylthiouracil embryopathy', 'PTU embryofetopathy', 'PTU embryopathy']",,,485358,,,,,,,,,
mondo:0044621,16p12.1p12.3 triplication syndrome,"['trip(16)(p12.1p12.3)', 'tetrasomy 16p12.1-p12.3', 'tetrasomy 16p12.1p12.3']",,,485405,,,,,,,,,
mondo:0044622,EMILIN-1-related connective tissue disease,,,,485418,,,,,,,,,
mondo:0044624,pediatric collagenous gastritis,['childhood-onset collagenous gastritis'],,,487809,,,,,,,,,
mondo:0044625,autosomal dominant charcot-marie-tooth disease type 2 due to DGAT2 mutation,['CMT2 due to DGAT2 mutation'],,,487814,,,,,,,,,
mondo:0044626,female infertility due to oocyte meiotic arrest,,,,488191,,"['-0.6616', '-0.8735', '0.107', '-0.7764', '-0.3455', '-0.4314', '-0.02571', '0.4714', '-0.4023', '-0.2578', '1.315', '-0.04724', '-0.04254', '1.372', '0.1871', '-0.1251', '-0.05948', '0.618', '-0.718', '-1.082', '-0.1354', '0.0449', '0.5215', '-0.6577', '0.4712', '-0.778', '0.1738', '0.03784', '-0.6274', '-0.1589', '0.4126', '-0.1747', '-0.3003', '-0.0068', '0.05634', '0.03256', '0.04172', '0.000716', '0.05685', '-0.2864', '0.1798', '0.467', '0.3638', '-0.2148', '0.6216', '-0.75', '0.3591', '-0.7114', '0.737', '0.3108', '-0.9272', '-0.0944', '0.1598', '0.5557', '-0.1608', '0.509', '0.4631', '0.2488', '-0.719', '0.4346', '0.1451', '0.9165', '-0.10913', '0.5166', '-0.455', '0.369', '-0.2085', '0.6323', '-1.327', '0.683', '-0.493', '0.2238', '-0.09296', '-0.3267', '0.1367', '0.6484', '0.4666', '0.3364', '-0.301', '0.3813', '-0.01733', '0.492', '0.04446', '-0.6553', '0.11804', '-0.536', '0.0451', '-0.2654', '0.3884', '-0.6875', '-0.49', '0.3552', '-0.3381', '1.1045', '0.5864', '-0.3325', '0.1979', '-0.2615', '-0.7925', '0.2305']",,,,,,,
mondo:0044627,acute macular neuroretinopathy,['AMNR'],,,488239,,,,,,,,,
mondo:0044628,six2-related frontonasal dysplasia,['SIX2-related FND'],,,488437,,,,,,,,,
mondo:0044629,congenital amyoplasia,['amyoplasia congenita'],,,488586,,,,,,,,,
mondo:0044631,early-onset familial noncirrhotic portal hypertension,,,,494348,,,,,,,,,
mondo:0044632,extracranial carotid artery aneurysm,"['Ecca', 'ECAA']",,,494424,,,,,,,,,
mondo:0044633,idiopathic pleuroparenchymal fibroelastosis,"['idiopathic pleuropulmonary fibroelastosis', 'IPPFE']",,,494428,,,,,,,,,
mondo:0044634,retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome,"['retinitis pigmentosa-deafness-premature aging-short stature-facial dysmorphism syndrome', 'short stature, hearing loss, retinitis pigmentosa, and distinctive facies']",0081175,617763,494439,C4540367,,,,,,,,
mondo:0044635,DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome,['DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome'],,,494444,,,,,,,,,
mondo:0044637,infantile-onset generalized dyskinesia with orofacial involvement,"['dyskinesia, limb and orofacial, infantile-onset', 'IOLOD', 'infantile-onset orofacial-trunk-limbs dyskinesia']",,616921,494526,C5567464,,,,,,,,
mondo:0044638,hypopharynx squamous cell carcinoma,"['hypopharyngeal squamous cell carcinoma', 'epidermoid carcinoma of the hypopharynx', 'squamous cell carcinoma of hypopharynx', 'hypopharyngeal epidermoid carcinoma', 'hypopharyngeal throat squamous cell cancer', 'epidermoid carcinoma of hypopharynx', 'squamous cell carcinoma of the hypopharynx']",,,494547,,,C4043,1001960,,,,,
mondo:0044640,Charcot-Marie-Tooth disease type 2T,"['CMT2T', 'AR-CMT2T', 'autosomal recessive axonal Charcot-Marie-Tooth disease type 2T']",,,495274,CN237675,,,,,,,,
mondo:0044641,9q33.3q34.11 microdeletion syndrome,"['Del(9)(q33.3q34.11)', 'monosomy 9q33.3q34.11', '9q33.3-q34.11 microdeletion syndrome', 'monosomy 9q33.3-q34.11', 'deletion 9q33.3q34.11']",,,495818,,,,,,,,,
mondo:0044642,c11orf73-related autosomal recessive hypomyelinating leukodystrophy,"['hypomyelinating leukodystrophy due to hikeshi deficiency', 'C11ORF73-related autosomal recessive hypomyelinating leukoencephalopathy']",,,495844,,,,,,,,,
mondo:0044643,congenital labioscrotal agenesis-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome,['congenital agenesis of labia majora or scrotum-cerebellar malformation-corneal dystrophy-facial dysmorphism syndrome'],,,495875,,,,,,,,,
mondo:0044644,congenital agenesis of the scrotum,"['congenital scrotal agenesis', 'congenital absence of the scrotum', 'congenital scrotal absence']",,,495879,,,,,,,,,
mondo:0044645,familial monosomy 7 syndrome,"['monosomy 7 myelodysplasia and leukaemia syndrome', 'monosomy 7 myelodysplasia and leukemia syndrome']",,,495930,,,,,,,,,
mondo:0044646,early-onset progressive diffuse brain atrophy-microcephaly-muscle weakness-optic atrophy syndrome,"['PEBAT', 'encephalopathy, progressive, early-onset, with brain atrophy and thin corpus callosum']",0070423,617193,496641,C4310671,,,,,,,,
mondo:0044647,kyphosis-lateral tongue atrophy-myofibrillar myopathy syndrome,,,,496686,,,,,,,,,
mondo:0044648,kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome,['kyphoscoliosis-lateral tongue atrophy-HSP syndrome'],,,496689,,,,,,,,,
mondo:0044649,omphalocele-diaphragmatic hernia-cardiovascular anomalies-radial ray defect syndrome,['Gershoni-Baruch syndrome'],,,496693,,,,,,,,,
mondo:0044651,early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome,,,,496756,,,,,,,,,
mondo:0044655,c12orf65-related combined oxidative phosphorylation defect,['C12ORF65-related COXPD'],,,497623,,,,,,,,,
mondo:0044656,epidermolytic nevus,"['epidermolytic epidermal nevus', 'epidermolytic verrucous epidermal nevus', 'Epidermal nevus with epidermolytic hyperkeratosis']",,,497737,C1302848,,,,,,,,
mondo:0044657,MME-related autosomal dominant Charcot Marie Tooth disease type 2,"['MME-related autosomal dominant CMT2', 'MME-related autosomal dominant hereditary motor and sensory neuropathy type 2']",,,497757,,,,,,,,,
mondo:0044660,menstrual cycle-dependent periodic fever,"['periodic fever, menstrual cycle dependent', 'luteal-phase-dependent periodic fever', 'menstrual cycle-dependent febrile episode', 'luteal-phase-dependent febrile episode', 'periodic fever, menstrual cycle-dependent']",,614674,498251,C3553418,,,,,,,,
mondo:0044663,aquagenic palmoplantar keratoderma,"['Transient reactive papulotranslucent acrokeratoderma', 'aquagenic wrinkling of the hands', 'aquagenic wrinkling of the palms', 'transient reactive papulotranslucent acrokeratoderma', 'aquagenic palmoplantar keratoderma', 'aquagenic keratoderma', 'aquagenic syringeal acrokeratoderma']",,,498359,,,,,,,,,
mondo:0044675,LRP5-related primary osteoporosis,,,,498481,,,,,,,,,
mondo:0044682,MYBPC1-related autosomal recessive non-lethal arthrogryposis multiplex congenita syndrome,['MYBPC1-related autosomal recessive non-lethal AMC syndrome'],,,498693,,,,,,,,,
mondo:0044685,autoimmune/inflammatory optic neuropathy,,,,499047,,,,,,,,,
mondo:0044687,chronic relapsing inflammatory optic neuropathy,"['chronic recurrent isolated optic neuritis', 'CRION']",,,499085,,,,,,,,,
mondo:0044688,isolated optic neuritis,['ion'],,,499096,,,,,,,,,
mondo:0044689,recurrent idiopathic neuroretinitis,['RINR'],,,499103,,,,,,,,,
mondo:0044690,optic perineuritis,['OPN'],,,499107,C4076165,,,,,,,,
mondo:0044696,early-onset progressive encephalopathy-hearing loss-pons hypoplasia-brain atrophy syndrome,"['encephalopathy, progressive, early-onset, with brain atrophy and spasticity', 'PEBAS']",,617669,500144,CN474476,,,,,,,,
mondo:0044699,SIN3A-related intellectual disability syndrome,,,,500163,,,,,,,,,
mondo:0044700,SIN3A-related intellectual disability syndrome due to a point mutation,,,,500166,,,,,,,,,
mondo:0044701,childhood-onset motor and cognitive regression syndrome with extrapyramidal movement disorder,"['neurodegeneration, childhood-onset, with brain atrophy', 'CONDBA', 'UBTF-related disorder']",,617672,500180,CN469330,,,,,,,,
mondo:0044702,X-linked external auditory canal atresia-dilated internal auditory canal-facial dysmorphism syndrome,"['DFNX7', 'deafness, X-linked 7, X-linked recessive', 'deafness, X-linked 7']",0111738,301018,500188,,,,,,,,,
mondo:0044704,oropharynx squamous cell carcinoma,"['oropharyngeal throat squamous cell cancer', 'oropharyngeal epidermoid carcinoma', 'epidermoid carcinoma of the oropharynx', 'epidermoid carcinoma of oropharynx', 'squamous cell carcinoma of the oropharynx', 'squamous cell carcinoma of oropharynx', 'oropharyngeal squamous cell carcinoma']",,,500478,,,C8181,,,,,,
mondo:0044705,paranasal sinus squamous cell carcinoma,"['epidermoid carcinoma of the paranasal sinus', 'squamous cell carcinoma of the nasal cavity and sinuses', 'paranasal sinus epidermoid carcinoma', 'squamous cell carcinoma of the paranasal sinus', 'paranasal sinus squamous cell carcinoma', 'squamous cell carcinoma of the nasal cavity and paranasal sinuses', 'squamous cell carcinoma of paranasal sinus', 'epidermoid carcinoma of paranasal sinus']",,,500464,C0280334,,C8193,,,,,,
mondo:0044709,cochleovestibular dysplasia,,,,502305,,,,,,,,,
mondo:0044710,lip and oral cavity squamous cell carcinoma,"['lip and oral cavity squamous cell cancer', 'lip and oral cavity squamous cell carcinoma', 'squamous cell carcinoma of oral cavity and lip', 'lip/oral cavity squam. cell car.']",,,502369,C0280297,,C42690,,,,,,
mondo:0044714,mitochondrial myopathy-cerebellar ataxia-pigmentary retinopathy syndrome,"['mitochondrial myopathy-cerebellar atrophy-pigmentary retinopathy syndrome', 'myopathy, mitochondrial, and ataxia', 'MMYAT']",,617675,502423,CN484737,,,,,,,,
mondo:0044715,metopic ridging-ptosis-facial dysmorphism syndrome,,,,502430,,,,,,,,,
mondo:0044717,4q25 proximal deletion syndrome,"['proximal monosomy 4q25', 'proximal del(4)(q25)']",,,502437,,,,,,,,,
mondo:0044718,alkaline ceramidase 3 deficiency,"['leukodystrophy due to alkaline ceramidase 3 deficiency', 'leukodystrophy, progressive, early childhood-onset', 'PLDECO', 'ACER3-related early childhood-onset progressive leukodystrophy']",,617762,502444,CN603947,"['-0.4521', '0.2017', '0.482', '-0.10455', '-0.04178', '-0.08136', '-0.03024', '0.5166', '-0.5405', '0.3357', '-0.1406', '-0.2021', '-0.01564', '-0.2568', '0.3298', '0.06305', '0.3132', '-0.2864', '-0.307', '-0.313', '0.04782', '-0.2343', '0.0224', '0.09595', '0.2229', '0.0408', '0.2319', '0.1725', '-0.0947', '-0.09436', '0.1691', '0.1582', '0.4478', '0.2256', '-0.0538', '0.1089', '-0.03323', '-0.1385', '0.0829', '-0.5596', '0.2156', '-0.3086', '-0.1324', '0.5376', '-0.01768', '-0.3513', '0.1228', '0.36', '-0.338', '-0.02078', '-0.2668', '0.108', '-0.2983', '-0.05997', '-0.2477', '-0.2898', '0.2318', '-0.4216', '-0.0915', '0.06946', '-0.1619', '0.2211', '-0.179', '0.3083', '-0.3633', '0.000298', '0.4822', '0.5757', '-0.01929', '0.6265', '-0.2805', '0.4585', '0.1451', '-0.0954', '-0.176', '-0.18', '0.297', '0.03287', '-0.3003', '-0.2344', '0.2627', '-0.255', '0.05237', '0.66', '-0.0636', '0.1573', '-0.03894', '0.2078', '0.3826', '0.00129', '0.292', '0.4607', '0.1964', '0.291', '0.4292', '0.183', '0.1567', '0.06903', '0.48', '0.277']",,,,,,,
mondo:0044719,erythema multiforme major,"['erythema exsudativum multiforme majus', 'erythema multiforme majus']",,,502499,,,C3385,,,,,,
mondo:0044720,cerebellar ataxia with neuropathy and bilateral vestibular areflexia syndrome,"['CABV syndrome', 'CANVAS', 'cerebellar ataxia, neuropathy, and vestibular areflexia syndrome', 'cerebellar ataxia with bilateral vestibulopathy syndrome']",,614575,504476,C3281223,,,,,,,,
mondo:0044721,severe combined immunodeficiency due to LAT deficiency,"['immunodeficiency 52', 'SCID due to LAT deficiency', 'IMD52']",0111983,617514,504523,C4479588,,,,,,,,
mondo:0044723,3-methylglutaconic aciduria type 8,"['MGCA8', '3-methylglutaconic aciduria, type VIII', '3-methylglutaconic aciduria type VIII', '3-methylglutaconic aciduria type VIII, MGCA8', 'MGA8', '3-Methylglutaconic aciduria, type 8']",0070000,617248,505208,C4310650,,,,,,,,
mondo:0044724,3-methylglutaconic aciduria type 9,"['MGCA9', '3-methylglutaconic aciduria-epilepsy-spasticity-severe intellectual disability syndrome', '3-Methylglutaconic aciduria, type 9', '3-methylglutaconic acuduria type IX, MGCA9', 'MGA9', '3-METHYLGLUTACONIC aciduria, type IX', '3-methylglutaconic acuduria type IX']",0070002,617698,505216,CN510468,"['-0.02538', '0.138', '-0.03116', '0.00725', '0.0652', '-0.1499', '-0.03174', '0.127', '-0.09863', '0.01315', '-0.07263', '0.00762', '0.02568', '-0.05627', '-0.01319', '-0.0636', '0.04385', '-0.0188', '-0.00526', '-0.1743', '-0.00516', '-0.08887', '0.07837', '-0.02692', '0.02669', '-0.03317', '-0.02896', '-0.05963', '-0.02762', '-0.03326', '0.101', '0.02159', '0.1036', '0.05124', '0.009026', '-0.01517', '-0.05087', '-0.0622', '-0.05197', '-0.04675', '0.03842', '-0.1598', '0.02261', '0.000794', '-0.04974', '-0.1003', '0.02654', '0.0662', '0.01492', '-0.0168', '-0.05002', '-0.07104', '-0.04636', '-0.0627', '-0.02467', '-0.01354', '0.1263', '-0.06384', '-0.09686', '0.0883', '0.08026', '0.003292', '0.0773', '-0.003101', '-0.00973', '0.0103', '0.1212', '0.03555', '-0.1484', '0.1532', '-0.05408', '0.02121', '-0.02153', '-0.079', '0.072', '0.0785', '-0.01636', '-0.00668', '-0.05338', '-0.06097', '0.0456', '-0.002312', '-0.04623', '0.05545', '0.012146', '0.04053', '0.0361', '0.184', '0.1377', '0.02011', '0.1008', '0.08984', '0.014465', '-0.003252', '0.2249', '0.1103', '0.0774', '-0.1295', '0.00045', '0.0242']",,,,,,,
mondo:0044725,combined immunodeficiency due to GINS1 deficiency,"['IMD55', 'immunodeficiency 55', 'combined immunodeficiency with intrauterine growth retardation-NK cell deficiency-neutropenia', 'combined immunodeficiency with intrauterine growth retardation-natural killer cell deficiency-neutropenia', 'CID due to GINS1 deficiency']",0111993,617827,505227,CN737162,"['-0.0298', '0.02684', '0.00548', '-0.00855', '0.02112', '-0.0266', '0.01598', '0.03226', '-0.01778', '-0.02841', '0.0002038', '-0.013374', '-0.00931', '0.002504', '-0.01123', '-0.02289', '-0.01352', '-0.001854', '-0.02655', '-0.0521', '-0.006683', '-0.015175', '0.03708', '-0.01776', '0.01015', '-0.005634', '-0.00368', '-0.01168', '-0.003181', '-0.03128', '0.02744', '0.00893', '0.03836', '0.006466', '0.00941', '-0.01517', '-0.006577', '-0.01207', '-0.001892', '-0.03198', '0.011505', '-0.02094', '0.011345', '-0.01166', '-0.01342', '-0.026', '-0.010544', '-0.00309', '0.00839', '0.02509', '3.56e-05', '-0.00878', '0.01074', '0.01302', '-0.01665', '0.006073', '0.02585', '-0.01379', '-0.04236', '0.01162', '0.02548', '0.01335', '-0.001624', '-0.003248', '0.010956', '0.0069', '0.0362', '0.0282', '-0.0407', '0.03833', '-0.0222', '0.005558', '0.000819', '-0.02466', '0.01423', '0.01527', '0.01341', '0.003899', '-0.01909', '-0.00725', '0.005943', '-0.00659', '-0.00865', '0.01104', '-0.001561', '-0.003895', '0.01429', '0.01651', '0.0577', '0.007366', '0.02367', '0.02322', '-0.008736', '-8.553e-05', '0.06464', '0.02768', '0.011696', '-0.03622', '0.002277', '0.00643']",,,,,,,
mondo:0044726,psychomotor regression-oculomotor apraxia-movement disorder-nephropathy syndrome,"['Cerebrorenal syndrome, Perez type', 'Birk-Landau-Perez syndrome', 'BILAPES']",,617595,505242,CN353477,,,,,,,,
mondo:0044727,pancreatic carcinoma with mixed differentiation,"['pancreatic MiNEN', 'MiNEN of pancreas', 'mixed exocrine-endocrine carcinoma of the pancreas', 'mixed neuroendocrine-nonneuroendocrine neoplasm of pancreas', 'pancreatic carcinoma with mixed differentiation', 'pancreatic mixed neuroendocrine-nonneuroendocrine neoplasm']",,,506112,C1709050,,C45843,,,,,,
mondo:0044737,autosomal recessive complex spastic paraplegia due to kennedy pathway dysfunction,['autosomal recessive complex SPG due to Kennedy pathway dysfunction'],0112349,,506353,,,,,,,,,
mondo:0044738,Gabriele de Vries syndrome,"['Gabriele-De Vries syndrome', 'GADEVS', 'YY1 haploinsufficiency syndrome', 'Gabriele-de Vries syndrome']",,617557,506358,C4479652,"['-0.05576', '0.05496', '0.033', '-0.0406', '0.006042', '-0.0842', '0.01746', '0.0901', '-0.0705', '-0.0339', '-0.03943', '-0.01903', '0.002224', '0.01099', '-0.014534', '-0.01857', '-0.00234', '-0.06824', '-0.01799', '-0.1328', '0.01143', '0.003744', '0.0718', '-0.04407', '0.0409', '-0.01865', '-0.02202', '-0.0167', '0.03094', '-0.02695', '0.05573', '-0.001308', '0.0877', '0.05624', '0.02061', '-0.05264', '0.006603', '-0.03604', '-0.02843', '-0.0854', '0.03119', '-0.0867', '0.01921', '-0.01949', '0.003593', '-0.06125', '-0.04095', '0.04453', '-0.02359', '0.0226', '-0.0211', '0.001689', '0.0009465', '0.02954', '-0.04523', '-0.02097', '0.1003', '-0.0432', '-0.0703', '0.02696', '0.02605', '0.02228', '-0.0323', '0.002155', '0.007835', '0.014885', '0.0724', '0.06573', '-0.053', '0.0878', '-0.1015', '0.01063', '0.01069', '-0.02263', '0.02513', '0.01692', '0.01033', '-0.03162', '-0.07465', '-0.0307', '0.0356', '0.01903', '-0.0291', '0.06067', '-0.00978', '0.00197', '0.00827', '0.10834', '0.0824', '0.0219', '0.03754', '0.067', '0.01953', '0.00525', '0.1567', '0.009674', '0.126', '-0.1443', '-0.000512', '0.03687']",,,,,,,
mondo:0044739,Stevens-Johnson syndrome/toxic epidermal necrolysis overlap syndrome,"['SJS/TEN overlap syndrome', 'Stevens-Johnson/TEN overlap syndrome', 'Stevens-Johnson/toxic epidermal necrolysis overlap syndrome']",,,506784,,,,,,,,,
mondo:0044740,salivary gland squamous cell carcinoma,"['epidermoid carcinoma of salivary gland', 'salivary gland squamous cell carcinoma', 'epidermoid carcinoma of the salivary gland', 'salivary gland SCC', 'squamous cell carcinoma of salivary glands', 'SCC of salivary gland', 'squamous cell carcinoma of the salivary gland', 'salivary gland epidermoid carcinoma', 'squamous cell carcinoma of salivary gland', 'salivary gland squamous cell cancer', 'SCC of the salivary gland']",,,500481,C0279697,,C7991,1001967,,,,,
mondo:0044742,autosomal recessive epidermolytic ichthyosis,['AREI'],,,512103,,,,,,,,,
mondo:0044743,major salivary gland cancer,"['cancer of major salivary gland', 'malignant neoplasm of major salivary gland', 'malignant tumor of the major salivary gland', 'malignant tumor of major salivary gland', 'malignant major salivary gland neoplasm', 'malignant major salivary gland tumor', 'malignant neoplasm of the major salivary gland', 'malignant major salivary gland tumour', 'malignant tumour of major salivary gland', 'malignant tumour of the major salivary gland']",,,,C0496763,,C4762,,,,,,
mondo:0044744,prekallikrein deficiency,['prekallikrein deficiency'],,,,,,C99022,,,,,,
mondo:0044745,nervous system injury,"['nervous system Injuries', 'nervous system Traumas', 'nervous system trauma', 'Injuries, craniocervical', 'nervous system injury', 'craniocervical injury', 'injury, craniocervical', 'Injuries, nervous system', 'injury, nervous system', 'craniocervical Injuries', 'injury of nervous system']",,,,,,,,D020196,,,,
mondo:0044748,anaplasmosis in cattle,['Anaplasmoses'],,,,,,,,,,,,
mondo:0044749,X-linked congenital stationary night blindness,"['X-linked CSNB', 'XLCSNB', 'congenital stationary night blindness, X-linked']",,,215,CN043584,"['-0.313', '-0.0697', '0.265', '0.1805', '0.4094', '-0.10657', '-0.3076', '0.1857', '-0.10846', '0.0961', '-0.09393', '0.1453', '-0.1865', '-0.1427', '-0.197', '-0.2573', '0.4001', '-0.0625', '0.1941', '-0.3372', '-0.2238', '-0.03134', '-0.06866', '0.06396', '-0.0819', '0.02885', '-0.3745', '-0.2372', '-0.2343', '0.243', '0.1615', '0.09155', '0.3296', '0.363', '-0.1951', '0.01408', '0.08636', '-0.1224', '-0.3665', '-0.4995', '0.2134', '-0.2566', '0.1497', '-0.3528', '-0.4912', '-0.1477', '0.08466', '0.1763', '-0.015114', '0.5034', '0.1863', '0.0677', '0.02733', '-0.2472', '0.03198', '-0.2617', '0.536', '-0.2197', '-0.389', '-0.05664', '0.0804', '-0.0417', '-0.0006785', '0.3037', '-0.0175', '0.03235', '0.712', '0.5566', '-0.04413', '0.3904', '-0.147', '0.3171', '0.3604', '-0.4514', '0.4397', '-0.1146', '0.0819', '-0.5327', '-0.02846', '0.0541', '0.0787', '-0.398', '0.007236', '0.717', '-0.0765', '0.010796', '-0.2229', '0.01993', '0.702', '0.002184', '0.2339', '0.491', '-0.1339', '-0.10724', '0.00905', '0.06076', '-0.1702', '-0.1675', '-0.12335', '0.3113']",,,,,,,
mondo:0044750,lassa virus infectious disease,,,,,C1617072,,,,,,,,
mondo:0044751,chronic diarrheal disease,"['chronic diarrhoea', 'diarrheal disease, chronic']",,,,C0401151,,,,,,,,
mondo:0044753,lumbar spinal stenosis,['lumbar region of vertebral column spinal stenosis'],,,,C0158288,,C177445,,,724.02,,,0004610
mondo:0044762,diarrheal disease secondary to increased bowel motility,"['motility-related diarrhoea', 'diarrhoea from increased bowel motility', 'motility-related diarrhea']",0050131,,,,,,,,,,,
mondo:0044763,diarrheal disease secondary to decreased bowel motility,['diarrhoea from decreased bowel motility'],,,,,,,,,,,,
mondo:0044764,benign choroid plexus neoplasm,"['benign tumor of choroid plexus', 'benign choroid plexus tumor', 'benign choroid plexus tumour', 'benign neoplasm of the choroid plexus', 'benign tumour of the choroid plexus', 'benign choroid plexus neoplasms', 'benign tumor of the choroid plexus', 'benign neoplasm of choroid plexus', 'benign choroid plexus tumours', 'benign tumour of choroid plexus', 'benign choroid plexus neoplasm', 'benign choroid plexus tumors']",,,,C0346290,,C8405,,,,,,
mondo:0044765,steroid-resistant nephrotic syndrome,"['nephrotic syndrome of childhood - steroid resistant', 'nephrotic syndrome, idiopathic, steroid-resistant', 'nephrotic syndrome-steroid-resistant', 'steroid-resistant nephrotic syndrome', 'NPHS2', 'nephrotic syndrome, steroid-resistant, autosomal recessive']",,,,CN034406,,C122798,,,,,,
mondo:0044767,childhood adrenal gland pheochromocytoma,"['malignant childhood adrenal gland pheochromocytoma', 'childhood adrenal gland pheochromocytoma', 'pheochromocytoma, childhood']",0070325,,,CN036354,,C118822,,,,,,
mondo:0044768,vagus nerve paraganglioma,"['paraganglioma of the vagus nerve', 'vagal body paraganglioma', 'vagus nerve paraganglioma', 'vagal paraganglioma', 'paraganglioma of vagus nerve', 'paraganglioma of the vagal body', 'paraganglioma of vagal body']",,,,CN036786,,C8427,1000621,,,,,
mondo:0044776,premature ovarian failure 10,"['Pof10', 'premature ovarian failure 10', 'menopause, natural, Age At, quantitative trait locus 3']",0080867,612885,,,,,,,,,,
mondo:0044777,premature ovarian failure 14,"['premature ovarian failure 14', 'GDF9-related primary ovarian insufficiency', 'POF14']",0080871,618014,,CN757793,,,,,,,,
mondo:0044778,nodular lymphocyte predominant Hodgkin lymphoma,"['NLPHL', 'nodular lymphocyte predominant Hodgkin lymphoma', 'Hodgkin lymphoma nodular LP, NOS', 'nodular lymphocyte-predominant Hodgkin lymphoma', 'nodular lymphocyte predominant Hodgkin^s lymphoma', 'Hodgkin lymphoma nodular lymphocyte predominant type, NOS']",,,86893,C1334968,,C7258,,,,,,
mondo:0044781,nephrotic syndrome of childhood - steroid sensitive,"['nephrotic syndrome of childhood - steroid sensitive', 'steroid-responsive nephrotic syndrome', 'steroid-sensitive nephrotic syndrome']",,,,C0403396,,C122797,,,,,,
mondo:0044782,esophageal ulcer,"['oesophagus ulcer disease', 'oesophagus ulcer', 'ulcer disease of esophagus', 'esophageal ulcer', 'ulcer disease of oesophagus', 'esophagus ulcer disease']",,,,,,C26950,,,,,,0004791
mondo:0044783,solid papillary breast carcinoma,"['solid Papillary carcinoma of the breast', 'solid Papillary breast carcinoma']",,,,,,C6870,,,,,,
mondo:0044784,myxoma,"['MYXOMA, BENIGN', 'Myxoma']",,,,,,C6577,,D009232,,,,
mondo:0044785,desmoplastic melanoma,"['desmoplastic cutaneous (skin) melanoma', 'desmoplastic melanoma']",,,,,,C37257,,,,,,
mondo:0044786,solid pseudopapillary neoplasm of the pancreas,"['Frantz tumour', 'solid pseudopapillary tumor of the pancreas', 'solid pseudopapillary tumour of the pancreas', 'solid pseudopapillary neoplasm of the pancreas', 'Frantz tumor']",,,,,,C37212,,,,,,
mondo:0044787,nasal cavity and paranasal sinus squamous cell carcinoma,"['nasal cavity and paranasal sinus squamous cell carcinoma', 'nasal cavity and paranasal sinus squamous cell cancer']",,,,C0280332,,C68611,,,,,,
mondo:0044788,perihilar intrahepatic cholangiocarcinoma,"['perihilar bile duct carcinoma', 'perihilar intrahepatic cholangiocarcinoma', 'perihilar ICC', 'perihilar cholangiocarcinoma']",,,,,,C96804,,,,,,
mondo:0012164,Meacham syndrome,"['Meacham syndrome', 'Meacham Winn Culler syndrome', 'Double vagina, cardiac, pulmonary, and other genital malformations with 46,XY karyotype', 'Rhabdomyomatous dysplasia-cardiopathy-genital anomalies syndrome', 'Meacham-Winn-Culler syndrome']",,608978,3097,C1837026,"['-0.408', '-0.507', '-0.506', '-0.661', '0.508', '-0.5146', '0.1697', '0.8574', '-0.3257', '-0.798', '-0.135', '-0.875', '-0.4814', '0.105', '-0.421', '0.02014', '-0.02917', '-0.1699', '-0.8916', '-0.457', '-0.369', '0.656', '0.5874', '-0.5786', '0.4265', '-0.3308', '-0.09576', '0.4846', '0.3982', '-0.0978', '1.098', '-0.1265', '0.598', '0.09827', '0.02086', '-0.803', '-0.0495', '-0.1294', '-0.1749', '-0.000131', '0.4465', '0.09705', '-0.1749', '-0.3271', '-0.1654', '-0.3557', '-0.4287', '-0.01551', '-0.3572', '0.04254', '0.1249', '-0.2395', '0.4258', '0.1755', '-0.634', '0.08307', '0.3079', '-0.2258', '0.1329', '-0.2515', '-0.1426', '0.4993', '0.2808', '0.692', '-0.595', '-0.126', '0.4514', '0.1511', '-0.9824', '0.4133', '-0.3235', '0.714', '-0.1029', '0.361', '0.1453', '-0.3687', '0.094', '-0.042', '-0.3018', '-0.1416', '0.299', '1.068', '0.8345', '0.1537', '-0.257', '-0.2139', '0.581', '0.3235', '-0.425', '-0.537', '-0.09845', '0.644', '-0.0651', '0.0929', '1.005', '-0.1137', '0.1415', '-0.4375', '-0.1483', '0.4077']",,,C538162,,,,
mondo:0012165,BNAR syndrome,"['bifid NOSE with or without anorectal and renal anomalies', 'bifid nose with or without anorectal and renal anomalies', 'BNAR']",,608980,217266,C4303547,"['-0.314', '-0.1536', '0.3418', '-0.331', '0.03314', '-0.2087', '0.07446', '0.2296', '-0.05417', '-0.1525', '0.1732', '-0.5815', '-0.175', '-0.3809', '-0.6406', '-0.2267', '-0.04947', '-0.4578', '0.02635', '-1.203', '-0.0564', '0.564', '0.5664', '-0.02684', '0.2969', '0.3442', '-0.51', '0.174', '1.16', '-0.333', '0.0751', '-0.4194', '0.2473', '0.3418', '0.3193', '-0.5957', '-0.672', '-0.2866', '-0.38', '-0.4478', '0.596', '-0.1504', '0.1617', '-0.6714', '0.0669', '-0.3445', '0.01417', '0.631', '-0.2073', '0.315', '-0.3127', '-0.3232', '0.04053', '-0.1398', '-0.839', '-0.0156', '-0.03958', '-0.002308', '-0.645', '0.4648', '0.6196', '0.1991', '0.03876', '0.08057', '0.1901', '-0.03038', '0.1709', '-0.1528', '-0.7725', '0.906', '-0.2394', '-0.05777', '0.3167', '0.02252', '-0.0512', '0.0781', '-0.09204', '-0.5522', '-0.476', '0.06604', '-0.05368', '0.4583', '-0.01231', '0.4204', '-0.09424', '-0.3972', '0.0703', '0.547', '-0.01826', '0.0728', '-0.2024', '0.501', '0.6167', '0.2136', '0.584', '-0.2861', '0.2294', '-0.588', '-0.06168', '0.8286']",,,C567672,,,,
mondo:0012166,autosomal dominant sensory ataxia 1,"['ADSA', 'ataxia, sensory, 1, autosomal dominant', 'Adsa', 'SNAX1', 'RNF170 hereditary ataxia', 'hereditary ataxia caused by mutation in RNF170']",0111170,608984,,C1837015,,,,,,,,
mondo:0012167,"atrial fibrillation, familial, 2","['atrial fibrillation, familial, 2', 'ATFB2']",,608988,,C1837812,,,,C563903,,,,
mondo:0012168,"dyslexia, susceptibility to, 8","['DYX8', 'dyslexia, susceptibility to, 8, multifactorial', 'dyslexia, susceptibility to, 8']",,608995,,,,,,,,,,
mondo:0012169,premature ovarian failure 3,"['premature ovarian failure 3', 'premature ovarian failure type 3', 'Pof3']",0080860,608996,,C1837008,,,,C563816,,,,
mondo:0012170,autosomal recessive nonsyndromic hearing loss 36,"['autosomal recessive nonsyndromic deafness type 36', 'DFNB36', 'autosomal recessive nonsyndromic deafness caused by mutation in ESPN', 'deafness, autosomal recessive 36, with or without vestibular involvement', 'autosomal recessive nonsyndromic deafness 36', 'deafness, autosomal dominant, without vestibular involvement', 'autosomal recessive deafness 36', 'deafness, autosomal recessive 36', 'ESPN autosomal recessive nonsyndromic deafness']",0110494,609006,,,,,,C563815,,,,
mondo:0012171,marfanoid habitus with situs inversus,['marfanoid habitus with situs inversus'],,609008,,C1836994,,,,C563814,,,,
mondo:0012172,mitochondrial trifunctional protein deficiency,"['trifunctional Protein deficiency with myopathy and neuropathy', 'mitochondrial trifunctional protein deficiency', 'trifunctional Protein deficiency', 'TFPD', 'TFP deficiency', 'mitochondrial trifunctional PROTEIN deficiency', 'MTPD']",0111277,609015,746,,"['0.2666', '0.216', '-0.3289', '0.1975', '0.2507', '-0.46', '-0.0698', '0.4746', '0.1829', '-0.01245', '0.1236', '0.02496', '0.05737', '0.1866', '-0.3215', '-0.1982', '0.0941', '-0.27', '-0.2693', '-0.673', '0.3755', '-0.85', '0.2998', '-0.2473', '-0.4922', '-0.01362', '-0.1802', '-0.341', '0.1398', '-0.302', '0.5205', '0.2927', '0.3057', '0.139', '-0.503', '-0.448', '-0.6084', '-0.3694', '-0.2751', '-0.0825', '-0.1572', '-0.9424', '0.911', '0.5063', '-0.144', '-0.7896', '-0.416', '-0.1813', '0.2269', '0.7534', '-0.5703', '0.247', '0.07715', '0.12134', '0.659', '-0.7437', '0.433', '-0.01862', '0.2632', '0.512', '0.2241', '-0.03732', '0.65', '0.1866', '-0.545', '0.6196', '0.406', '1.121', '-0.3325', '-0.003176', '0.04846', '0.3953', '0.1375', '0.6865', '0.1517', '0.6523', '0.4167', '-0.0775', '0.3074', '0.09296', '0.0749', '-0.606', '-0.3174', '-0.3171', '0.2805', '1.049', '-0.1996', '0.3228', '0.6753', '0.2822', '1.009', '-0.08356', '0.01569', '0.3682', '0.264', '0.442', '0.6333', '-0.363', '-0.06494', '-0.3298']",C98991,,C566945,277.85,,,
mondo:0012173,long chain 3-hydroxyacyl-CoA dehydrogenase deficiency,"['LCHADD', 'long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency', 'fatty liver, acute, of pregnancy', 'LCHAD deficiency', 'long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency', 'long-chain 3-OH acyl-CoA dehydrogenase deficiency', 'long-chain 3-hydroxy acyl CoA dehydrogenase deficiency', 'trifunctional protein deficiency type 1', 'HELLP syndrome, maternal, of pregnancy', '3-hydroxyacyl-CoA dehydrogenase long chain deficiency']",,609016,5,CN239369,"['0.6914', '0.2957', '-0.5195', '0.048', '0.2039', '-0.4634', '0.05624', '0.868', '0.005894', '-0.6304', '-0.1903', '-0.09906', '-0.07086', '0.11945', '-0.4973', '-0.10834', '-0.2035', '-0.623', '-0.4844', '-0.7124', '-0.1613', '-0.665', '0.5356', '-0.2917', '-0.577', '-0.1617', '0.259', '-0.32', '0.2393', '-0.346', '0.5957', '0.3335', '0.5923', '0.2646', '-0.624', '-0.3667', '-0.04636', '-0.3572', '-0.594', '0.2947', '-0.235', '-0.4824', '0.5796', '-0.02956', '-0.4934', '-0.255', '-0.04272', '0.318', '0.362', '0.7363', '-0.4539', '0.0853', '0.097', '-0.3538', '0.4055', '-0.4893', '0.4463', '0.1071', '0.2983', '0.2947', '0.349', '0.2466', '0.788', '0.0399', '-0.431', '0.4653', '0.575', '0.7173', '-0.498', '-0.4448', '-0.5015', '0.6', '-0.2666', '0.2666', '-0.3022', '0.4028', '0.65', '0.000195', '0.1421', '-0.31', '0.4714', '-0.3877', '-0.467', '-0.534', '0.01514', '0.604', '-0.1621', '-0.3376', '0.703', '-0.2708', '0.4338', '-0.00173', '-0.082', '0.7417', '0.06305', '-0.05908', '0.313', '-0.1602', '-0.4202', '-0.335']",C129929,,,,,,
mondo:0012174,peripheral cone dystrophy,['peripheral cone dystrophy'],,609021,,C1836946,,,,C563813,,,,
mondo:0012175,cataract 28,"['age-related cortical cataract 1', 'cataract, age-related cortical, 1', 'cataract type 28', 'cataract 28, age-related cortical, susceptibility to', 'cataract 28', 'ARCC1', 'CTRCT28']",0110244,609026,,C1836942,,,,C563812,,,,
mondo:0012176,Emanuel syndrome,"['supernumerary der(22) syndrome', 'Ehlers-Danlos syndrome, classic-like, 1', 'Der(22)t(11;22) syndrome', 'supernumerary Der(22)T(11', 'Emanuel syndrome', 'supernumerary der(22),t(11;22) syndrome']",,609029,96170,C1836929,,,,C535733,758.5,,,
mondo:0012177,posterior column ataxia-retinitis pigmentosa syndrome,"['autosomal recessive posterior column ataxia and retinitis pigmentosa', 'Pcarp', 'AXPC1', 'POSTERIOR column ataxia with retinitis pigmentosa', 'ataxia, posterior column, with retinitis pigmentosa', 'PCARP']",,609033,88628,C4510304,"['-0.1766', '-0.01663', '-0.1139', '0.0428', '-0.3179', '-0.7837', '0.256', '0.2268', '-0.7964', '-1.164', '-0.04684', '0.1819', '-0.06964', '0.0904', '0.4768', '-0.5493', '0.10895', '0.02075', '0.1996', '-0.909', '-0.0929', '-0.4236', '0.02626', '-0.4524', '0.472', '-0.289', '-0.3909', '0.149', '-0.1924', '-0.741', '0.244', '0.2766', '-0.999', '-0.4985', '0.71', '0.0664', '-0.0465', '0.005974', '0.4548', '0.6973', '0.4236', '0.03177', '-0.418', '0.1107', '0.663', '-0.4077', '0.2854', '0.5117', '0.2522', '0.00204', '-0.2262', '0.1033', '0.02144', '-0.3767', '0.06125', '-0.9717', '0.518', '0.478', '-0.1592', '0.5483', '-0.4646', '0.1154', '0.32', '-0.1821', '-0.3052', '0.4338', '0.4045', '0.748', '-0.5117', '0.474', '0.4692', '0.5464', '-0.0926', '-0.6655', '0.713', '0.063', '0.4958', '0.1456', '0.297', '0.627', '-0.1853', '-0.8145', '0.3108', '0.8696', '-0.0746', '-0.6', '0.451', '-0.057', '0.4355', '0.254', '0.4915', '0.43', '0.3135', '0.0875', '0.955', '0.5635', '0.504', '0.4143', '-0.259', '-0.03186']",,,C536343,,,,
mondo:0012178,"intellectual disability with optic atrophy, facial dysmorphism, microcephaly, and short stature","['mental retardation with optic atrophy, facial dysmorphism, microcephaly, and short stature', 'intellectual disability with optic atrophy, facial dysmorphism, microcephaly, and short stature']",,609037,,C1836915,,,,C563810,,,,
mondo:0012179,narcolepsy 3,"['narcolepsy 3', 'NRCLP3']",,609039,,C1836907,,,,,,,,
mondo:0012180,arrhythmogenic right ventricular dysplasia 9,"['arrhythmogenic right ventricular cardiomyopathy 9', 'familial arrhythmogenic right ventricular dysplasia 9', 'arrhythmogenic right ventricular dysplasia, familial, type 9', 'ARVC9', 'PKP2 familial isolated arrhythmogenic right ventricular dysplasia', 'familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in PKP2', 'ARVD9', 'arrhythmogenic right ventricular dysplasia, familial, 9', 'arrhythmogenic right ventricular dysplasia type 9']",0110077,609040,,C1836906,,,,C563808,,,,
mondo:0012181,hereditary spastic paraplegia 27,"['spastic paraplegia 27, autosomal recessive', 'hereditary spastic paraplegia type 27', 'SPG27', 'autosomal recessive spastic paraplegia type 27', 'autosomal recessive spastic paraplegia 27']",0110778,609041,101007,C1836899,,,,C563807,,,,
mondo:0012182,"skeletal dysplasia, rhizomelic, with retinitis pigmentosa","['skeletal dysplasia, rhizomelic, with retinitis pigmentosa']",,609047,,C1836898,,,,C563806,,,,
mondo:0012183,"melanoma, cutaneous malignant, susceptibility to, 3","['melanoma, cutaneous malignant, susceptibility to, 3', 'melanoma, cutaneous malignant, susceptibility to, type 3', 'melanoma, cutaneous malignant, 3', 'CMM3', 'susceptibility to cutaneous malignant melanoma 3']",,609048,,,,,,,,,,
mondo:0012184,Pierson syndrome,"['microcoria-congenital nephrosis syndrome', 'Pierson syndrome', 'microcoria - congenital nephrotic syndrome', 'microcoria - congenital nephrosis', 'microcoria-congenital nephrotic syndrome']",0060852,609049,2670,C1836876,"['-0.02583', '-0.2524', '-0.3455', '-0.285', '-0.0863', '-0.005184', '-0.6763', '0.6074', '-0.7793', '-0.4927', '-0.275', '-0.4006', '0.02791', '0.268', '-0.2644', '0.000692', '-0.1587', '0.1423', '0.467', '-1.032', '0.3733', '-0.07666', '0.3125', '0.1074', '-0.0749', '-0.4985', '-0.6787', '1.187', '-0.1023', '0.1669', '0.6187', '0.003857', '0.2091', '0.1604', '0.02342', '-0.6055', '0.08057', '-0.3176', '0.1273', '0.0821', '-0.03111', '-0.3389', '0.4875', '0.01666', '0.2086', '-0.4167', '-0.06573', '-0.459', '0.2788', '-0.2869', '0.10626', '0.2925', '0.1611', '-0.43', '0.3333', '-0.4707', '0.809', '-0.1443', '-0.6', '0.11', '-0.1627', '-0.2847', '-0.2517', '-0.1931', '-0.2178', '-0.912', '0.56', '0.5083', '-0.4744', '-0.03146', '-0.01631', '0.2074', '-0.002848', '0.5264', '0.5225', '-0.7183', '0.526', '0.2415', '-0.142', '0.3154', '0.5645', '0.6587', '0.1095', '0.7925', '-0.5044', '0.397', '0.4214', '0.1771', '0.3386', '0.7437', '0.03906', '0.59', '-0.247', '0.5215', '0.253', '-0.04025', '0.3445', '-0.3872', '0.1309', '0.06122']",C128145,,C537185,,,,
mondo:0012185,"spondylometaphyseal dysplasia, A4 type","['spondylometaphyseal dysplasia type A4', 'spondylometaphyseal dysplasia, type A4', 'spondylometaphyseal dysplasia A4 type']",0112301,609052,168555,C1836862,,,,C563803,,,,
mondo:0012186,Fanconi anemia complementation group I,"['FANCI', 'Fanconi anaemia complementation group type I', 'Fanconi Anemia, complementation Group 1', 'Fanconi Anemia, complementation group type 1', 'Fanconi anemia, complementation group I', 'Fanconi anemia complementation group type I']",0111091,609053,,C1836861,,C129026,,C563802,,,,
mondo:0012187,Fanconi anemia complementation group J,"['Fanconi anaemia complementation group type J', 'Fanconi anemia, complementation group J', 'Fanconi Anemia, complementation group type J', 'Fanconi anemia complementation group type J', 'FANCJ']",0111097,609054,,C1836860,,C129027,,C563801,,,,
mondo:0012188,neuronal ceroid lipofuscinosis 9,"['CLN9 disease', 'neuronal ceroid lipofuscinosis type 9', 'CLN9', 'ceroid lipofuscinosis, neuronal, 9', 'CLN 9']",0110733,609055,228357,,,,,C537953,,,,
mondo:0012190,nephrotic syndrome - deafness - pretibial epidermolysis bullosa syndrome,"['nephropathy with pretibial epidermolysis bullosa and deafness', 'epidermolysis bullosa simplex 7, with nephropathy and deafness', 'nephrotic syndrome-hearing loss-pretibial epidermolysis bullosa syndrome']",,609057,300333,C1836823,"['0.8066', '0.05865', '-0.1567', '-0.0829', '0.01807', '-0.576', '-0.664', '0.611', '-0.02483', '-0.852', '0.353', '-0.4275', '-0.8457', '0.5537', '-0.6914', '-0.0909', '-0.01242', '-0.8438', '-0.1678', '-0.7183', '-0.1427', '-0.1581', '0.1886', '0.6777', '0.4504', '0.076', '-0.8677', '0.6816', '-0.1569', '-0.874', '0.241', '-0.08575', '-0.05252', '-0.1694', '-0.00903', '-0.1973', '-1.163', '0.378', '1.091', '-0.4873', '0.2542', '-0.4536', '0.3674', '0.0451', '0.03476', '-0.3608', '-0.47', '0.1552', '0.3828', '-0.2852', '-0.5713', '-0.51', '0.5576', '0.00491', '-0.2496', '-0.531', '-0.1337', '1.002', '-0.868', '-0.2404', '0.01542', '0.301', '-0.02582', '0.323', '0.8955', '0.5073', '0.145', '0.1909', '-0.749', '0.2324', '-0.07544', '0.1219', '-0.444', '-0.178', '-0.03027', '-0.1049', '0.02795', '0.1803', '0.05087', '-0.09094', '-1.083', '0.345', '-0.09393', '-0.1122', '0.2118', '0.224', '-0.9277', '0.746', '0.826', '0.515', '-0.4434', '0.4653', '0.00782', '0.4167', '-0.1354', '0.63', '0.3025', '-0.5684', '0.699', '0.249']",,,C563798,,,,
mondo:0012191,hepatoencephalopathy due to combined oxidative phosphorylation defect type 1,"['Hepatoencephalopathy due to COXPD1', 'combined oxidative phosphorylation deficiency caused by mutation in GFM1', 'combined oxidative phosphorylation deficiency type 1', 'Hepatoencephalopathy, early fatal progressive', 'COXPD1', 'GFM1 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 1']",0111474,609060,137681,C1836797,"['-0.9707', '-0.07434', '0.4067', '-0.4858', '-0.03156', '-0.6304', '0.1926', '0.4204', '-0.451', '0.335', '-0.59', '-0.723', '-0.1326', '-0.3435', '-0.1981', '-0.3972', '0.4067', '-0.37', '-0.3992', '-0.833', '0.1908', '-0.8774', '0.2386', '-0.1328', '-0.4253', '-0.2798', '0.1719', '0.2402', '-0.0271', '-0.1306', '0.1019', '0.7676', '0.824', '0.083', '-0.3176', '0.0788', '0.03705', '-0.07166', '-0.1617', '0.0947', '0.3809', '-0.0421', '0.0431', '0.6484', '-0.74', '-0.0769', '0.0725', '-0.1572', '-0.001492', '0.1204', '-0.463', '0.1176', '-0.07056', '-0.11884', '-0.438', '-0.1683', '-0.0633', '-0.2935', '-0.316', '0.3745', '-0.02965', '-0.10864', '0.3928', '-0.0754', '-0.5303', '-0.0965', '0.7007', '0.536', '-0.708', '0.3472', '-0.6914', '0.703', '-0.4333', '-0.1594', '0.02917', '-0.05902', '0.6133', '-0.2128', '0.0668', '0.2336', '0.0435', '-0.000801', '-0.4287', '0.1832', '0.0823', '0.1172', '0.461', '0.536', '0.263', '-0.0806', '0.653', '0.2438', '-0.2489', '0.278', '0.5776', '0.92', '0.0897', '-0.1895', '0.5015', '0.2822']",C125663,,C563797,,,,
mondo:0012192,permanent neonatal diabetes mellitus-pancreatic and cerebellar agenesis syndrome,"['diabetes mellitus, permanent neonatal, with cerebellar agenesis', 'pancreatic and cerebellar agenesis', 'paca']",,609069,65288,C1836780,"['0.7764', '-0.10876', '0.04138', '0.828', '-0.4382', '-0.9717', '-0.2886', '0.9683', '0.03006', '-0.5938', '0.2325', '-0.407', '0.386', '-0.006653', '-0.8857', '-0.4402', '0.592', '0.3071', '-0.1819', '-0.5874', '0.2546', '-0.0775', '0.0112', '0.1112', '-0.697', '-0.328', '0.1241', '0.05093', '0.6616', '-0.5605', '0.917', '-0.704', '0.1908', '-0.324', '-0.11835', '0.557', '-0.683', '0.4128', '0.0476', '-0.2615', '-0.03105', '0.3228', '0.1088', '0.567', '-0.4402', '-0.4858', '0.4727', '-0.1768', '0.1234', '0.1667', '0.2717', '-0.3152', '0.791', '-0.767', '-0.08575', '0.10736', '-0.1531', '-0.8457', '-1.074', '0.6807', '-0.4983', '0.543', '-0.1475', '0.08746', '-0.326', '0.8384', '-0.4912', '0.587', '-0.963', '0.2583', '0.3848', '0.3984', '0.1597', '-0.1884', '0.407', '0.4285', '-0.59', '1.036', '-0.2747', '-0.1185', '0.1603', '0.3518', '-0.2013', '-0.4236', '0.1367', '0.3225', '-0.02135', '0.597', '0.7656', '0.1859', '0.6157', '0.5312', '0.1709', '-0.2124', '1.228', '0.2175', '-0.2583', '-0.05215', '-0.4316', '0.176']",,,C563796,,,,
mondo:0012193,autosomal dominant limb-girdle muscular dystrophy type 1G,"['autosomal dominant limb-girdle muscular dystrophy caused by mutation in HNRNPDL', 'muscular dystrophy, limb-girdle, autosomal dominant 3', 'HNRNPDL autosomal dominant limb-girdle muscular dystrophy', 'limb-girdle muscular dystrophy type 1G', 'muscular dystrophy limb-girdle type 1G', 'limb-girdle muscular dystrophy, type 1G', 'LGMD1G']",0110306,609115,55596,,"['0.249', '-0.56', '-0.512', '-0.4084', '0.703', '-1.244', '0.3223', '0.7876', '-1.747', '-0.803', '-0.01964', '0.2194', '-0.264', '0.8496', '0.1931', '0.2656', '-0.6953', '-0.4937', '-0.731', '-0.8716', '0.073', '0.1538', '0.1414', '0.524', '0.3179', '0.1923', '-0.1743', '-0.9478', '0.2477', '-0.6455', '0.8325', '-0.03522', '0.3809', '0.1703', '-0.02776', '-0.2076', '-0.4585', '0.2178', '0.216', '-0.4487', '0.1486', '-0.5757', '-0.561', '0.2507', '-0.5674', '0.0723', '0.0977', '0.6733', '0.03372', '0.5073', '0.3994', '-0.2837', '0.4321', '-0.86', '0.0543', '-0.649', '0.286', '0.502', '-0.0709', '0.0378', '0.353', '0.16', '-0.1349', '-0.2383', '-0.1794', '0.1433', '0.06433', '0.664', '-0.474', '-0.3938', '-0.2399', '0.6807', '0.4805', '-0.1567', '0.6553', '0.8237', '0.11926', '0.5327', '-0.11255', '0.0385', '-0.0498', '0.2468', '-0.0506', '-0.2126', '-0.2021', '0.1832', '-0.4116', '-0.1969', '0.7095', '0.06915', '-0.3774', '0.04913', '0.1758', '1.018', '-0.2852', '0.3276', '0.3655', '-0.434', '-0.3633', '0.2998']",,,C563794,,,,
mondo:0012194,"aneurysm, intracranial berry, 3","['ANIB3', 'aneurysm, intracranial BERRY, 3']",0080966,609122,,C1836757,,,,C563792,,,,
mondo:0012195,arthrogryposis-severe scoliosis syndrome,"['arthrogryposis with Severe scoliosis', 'arthrogryposis, distal, type 2D', 'distal arthrogryposis type IID', 'distal arthrogryposis type 4', 'arthrogryposis, distal, type 4', 'DA4']",0111610,609128,65720,C1836756,,,,C563791,,,,
mondo:0012196,autosomal dominant auditory neuropathy 1,"['NSDAN', 'autosomal dominant auditory neuropathy type 1', 'auditory neuropathy, autosomal dominant, type 1', 'auditory neuropathy, autosomal dominant, 1', 'nonsyndromic dominant auditory neuropathy', 'DIAPH3 auditory neuropathy', 'auditory neuropathy, nonsyndromic dominant', 'AUNA1', 'auditory neuropathy caused by mutation in DIAPH3']",0060690,609129,,C1836743,,,,C563790,,,,
mondo:0012197,idiopathic aplastic anemia,"['secondary aplastic anemia', 'aplastic Anemia, susceptibility to', 'aplastic anemia', 'aplastic anemia idiopathic', 'anemia aplastic', 'anaemia aplastic', 'secondary aplastic anaemia', 'idiopathic aplastic aplasia', 'idiopathic bone marrow failure', 'aplastic anaemia', 'aplastic anaemia idiopathic']",,609135,88,C0348890,"['0.002813', '-0.0003831', '0.006584', '-0.00175', '0.01567', '-0.02252', '0.00991', '0.02092', '-0.01421', '0.001615', '0.003052', '-0.00787', '0.001259', '0.004623', '0.002058', '-0.007324', '-0.009895', '-0.00779', '-0.013374', '-0.02574', '0.002645', '-0.01328', '0.00496', '-0.01009', '-0.003725', '0.001006', '0.00861', '-0.012474', '-0.001965', '-0.0066', '0.01476', '-0.013054', '0.01183', '0.01191', '0.01053', '-0.01023', '-0.014626', '-0.01735', '-0.0004444', '-0.01386', '-0.0002978', '-0.002565', '-0.001521', '-0.01258', '0.004635', '-0.0106', '-0.00895', '0.002962', '0.003338', '-8.3e-05', '-0.0004807', '-0.000746', '0.00872', '-0.001715', '-0.01096', '-0.01095', '-0.002577', '0.002337', '-0.004154', '-0.003843', '0.00856', '0.001079', '0.01126', '-0.0012455', '-0.001658', '0.00616', '0.01483', '0.00828', '-0.01761', '0.01682', '0.002485', '0.005302', '-0.004436', '-0.01468', '-0.00404', '-0.00389', '-0.00722', '0.00477', '-0.006733', '-0.004486', '-0.001602', '0.007294', '-0.005108', '-0.001593', '-0.001734', '-0.00838', '0.00242', '0.004738', '0.004913', '0.01223', '-0.001337', '0.00937', '0.00999', '0.003458', '0.03075', '0.00509', '0.00523', '-0.01238', '0.0059', '0.01264']",C61230,,C538494,,D61.3,,
mondo:0012198,PCWH syndrome,"['peripheral demyelinating neuropathy, central dysmyelination, Waardenburg syndrome, and Hirschsprung disease', 'peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Waardenburg syndrome-Hirschsprung disease', 'peripheral demyelinating neuropathy-central dysmyelinating leukodystrophy-Hirschsprung disease-Waardenburg syndrome', 'neurologic Waardenburg-Shah syndrome', 'PCWH', 'WS4 plus', 'Waardenburg-Shah syndrome, neurologic variant']",0090111,609136,163746,CN239463,"['0.3113', '0.6084', '-0.1163', '-0.1102', '0.1641', '-0.4421', '-0.01339', '0.01805', '0.05515', '0.2664', '-0.5054', '-0.4702', '-0.2832', '-0.1602', '0.1445', '-0.1826', '0.4468', '-0.4707', '-0.5986', '-0.586', '0.3574', '-0.2443', '-0.1506', '-0.01733', '-0.0958', '0.1681', '0.0711', '0.2294', '0.698', '0.1205', '0.447', '-0.04108', '0.2418', '0.2181', '0.0495', '-0.2223', '-0.08636', '-0.6445', '-0.393', '0.0098', '0.2352', '-0.3052', '0.459', '-0.01286', '-0.03748', '-1.052', '0.1472', '0.1616', '-0.7715', '-0.0971', '0.197', '0.3687', '-0.2225', '-0.2993', '0.0704', '0.4695', '0.5615', '0.1039', '-0.2438', '0.2211', '-0.0986', '0.2986', '0.3035', '0.5034', '-0.479', '0.481', '-0.0993', '0.9214', '-0.2493', '0.6387', '-0.698', '0.04486', '0.258', '0.2351', '0.3894', '-0.4219', '0.582', '-0.2092', '0.1954', '-0.3345', '0.2615', '-0.515', '-0.516', '0.72', '-0.0477', '0.1915', '0.09705', '0.8115', '0.3447', '0.1378', '1.159', '0.276', '0.3296', '-0.05948', '0.5728', '-0.1332', '0.4207', '-0.254', '0.3699', '0.341']",,,C563789,,,,
mondo:0012199,posterior polymorphous corneal dystrophy 2,"['corneal dystrophy, posterior polymorphous 2', 'corneal dystrophy, POSTERIOR polymorphous, 2', 'Ppcd2', 'corneal dystrophy, posterior polymorphous, type 2', 'posterior polymorphous corneal dystrophy caused by mutation in COL8A2', 'PPCD2', 'COL8A2 posterior polymorphous corneal dystrophy', 'posterior polymorphous corneal dystrophy type 2']",0110856,609140,,C1852795,,,,C565176,,,,
mondo:0012200,posterior polymorphous corneal dystrophy 3,"['posterior polymorphous corneal dystrophy type 3', 'PPCD3', 'corneal dystrophy, POSTERIOR polymorphous, 3', 'Ppcd3', 'corneal dystrophy, posterior polymorphous, type 3', 'ZEB1 posterior polymorphous corneal dystrophy', 'posterior polymorphous corneal dystrophy caused by mutation in ZEB1']",0110857,609141,,C1836724,,,,C563788,,,,
mondo:0012202,"malaria, mild, susceptibility to","['susceptibility to mild malaria', 'malaria, mild, susceptibility to', 'Mals']",,609148,,,,,,,,,,
mondo:0012203,familial hyperthyroidism due to mutations in TSH receptor,"['hyperthyroidism, congenital Nonautoimmune', 'Nonautoimmune hyperthyroidism', 'resistance to thyroid stimulating hormone', 'familial non-immune hyperthyroidism', 'toxic thyroid hyperplasia, autosomal dominant', 'hyperthyroidism, NONAUTOIMMUNE', 'hyperthyroidism, Nonautoimmune, autosomal dominant']",0081101,609152,424,C1836706,"['-0.3323', '-0.04233', '-0.362', '-0.05783', '-0.03265', '-0.2766', '0.3606', '0.2952', '-0.2913', '-0.1255', '0.06198', '0.01756', '0.03387', '-0.1088', '-0.07806', '0.1065', '-0.05164', '-0.05396', '-0.036', '-0.1975', '0.02454', '0.1224', '0.3892', '-0.1776', '0.1121', '0.2554', '0.2522', '-0.19', '-0.0798', '-0.3647', '0.3816', '0.364', '0.273', '0.12177', '-0.2686', '-0.2825', '-0.2751', '-0.2118', '-0.1884', '-0.1588', '0.3923', '0.00524', '0.329', '-0.0891', '0.1265', '-0.312', '-0.2184', '0.1505', '-0.05615', '0.3984', '-0.02032', '-0.0468', '0.3208', '-0.2646', '-0.406', '0.1255', '0.1735', '-0.3381', '-0.323', '-0.04788', '0.1854', '0.1356', '0.1252', '-0.509', '0.1189', '0.3252', '0.08014', '0.322', '-0.4133', '0.386', '-0.03183', '-0.1349', '-0.1626', '-0.09314', '0.186', '-0.01593', '0.2339', '-0.0723', '0.1221', '0.07544', '-0.251', '0.1254', '-0.3435', '-0.0713', '0.0673', '-0.1324', '0.2328', '0.4773', '0.198', '0.0263', '-0.00772', '0.1725', '-0.1309', '-0.1681', '0.5454', '-0.0946', '0.3174', '-0.624', '-0.09973', '0.2961']",,,C563786,,,,
mondo:0012204,familial pseudohyperkalemia,"['cryohydrocytosis, mild', 'pseudohyperkalemia Falkirk', 'pseudohyperkalemia, familial, 2, due to red cell leak', 'pseudohyperkalemia Chiswick', 'pseudohyperkalemia East London', 'PSHK2', 'pseudohyperkalemia Lille']",,609153,90044,C4273970,"['-0.5503', '-0.1127', '-0.5947', '0.4006', '-0.3447', '0.0766', '-0.6445', '0.6714', '-0.3494', '-0.7725', '0.3914', '0.2169', '0.0625', '0.1436', '-0.5005', '0.1781', '-0.2607', '-0.1263', '0.2352', '-0.4167', '-0.1943', '0.01855', '0.2957', '0.2654', '0.7207', '0.253', '-0.3018', '-0.2563', '0.05978', '0.05423', '0.2415', '-0.5635', '0.3152', '0.9404', '-0.4897', '-0.494', '-0.05566', '0.1735', '0.7314', '-0.4436', '-0.07544', '-0.5806', '0.5215', '-0.6587', '0.4375', '-0.534', '-0.598', '-0.553', '0.02402', '-0.3513', '0.1211', '-0.4214', '-0.316', '0.08484', '0.2688', '0.7974', '0.396', '-0.314', '0.0683', '0.26', '0.07654', '-0.09326', '0.4473', '-0.0821', '0.01016', '-0.1372', '0.1788', '0.1847', '-0.3435', '0.4329', '0.1423', '0.729', '-0.569', '0.705', '0.3916', '0.2191', '0.237', '0.1006', '0.034', '-1.127', '0.1891', '0.562', '0.4', '-0.1611', '-0.5137', '0.1384', '-0.2365', '0.2117', '0.1605', '-0.002445', '0.5396', '0.1943', '0.2783', '-0.1442', '1.012', '1.178', '0.4036', '-1.457', '-0.2301', '0.3132']",,,C563785,,,,
mondo:0012205,autosomal dominant striatal neurodegeneration type 1,"['striatal Degeneration, autosomal dominant 1', 'ADSD', 'striatal degeneration, autosomal dominant 1', 'autosomal dominant striatal neurodegeneration', 'PDE8B striatal degeneration, autosomal dominant', 'striatal degeneration, autosomal dominant', 'striatal degeneration, autosomal dominant caused by mutation in PDE8B', 'ADSD1']",,609161,,,,,,,,,,
mondo:0012206,"Czech dysplasia, metatarsal type","['Czech dysplasia', 'spondyloepiphyseal dysplasia with precocious osteoarthritis', 'pseudorheumatoid dysplasia, progressive, with hypoplastic toes', 'Czech dysplasia, metatarsal type', 'Czech dysplasia metatarsal type', 'pseudorheumatoid dysplasia progressive, with hypoplastic toes']",,609162,137678,,,,,C535766,,,,
mondo:0012207,"umbilicus, familial flat","['flat umbilicus familial', 'flat umbilicus, autosomal dominant', 'umbilicus, familial flat', 'flat umbilicus autosomal dominant']",,609164,,C1836682,,,,C537059,,,,
mondo:0012208,congenital reticular ichthyosiform erythroderma,"['erythroderma, ichthyosiform, congenital reticular', 'ichthyosis with confetti', 'CRIE', 'erythrokeratoderma, reticular', 'Aarau disease', 'ichthyosis variegata', 'IWC']",,609165,281190,C3665704,"['-0.09155', '0.1431', '-0.008705', '-0.04233', '0.11694', '-0.1974', '-0.0629', '0.07794', '-0.08655', '-0.063', '-0.0348', '-0.04276', '-0.0631', '-0.003393', '-0.052', '-0.01767', '0.0672', '-0.0689', '-0.02956', '-0.3218', '-0.0566', '-0.00846', '0.0918', '-0.0594', '0.014595', '0.02371', '-0.1471', '0.01418', '0.0215', '-0.0913', '0.11127', '0.03232', '0.1475', '0.1389', '0.0757', '-0.00474', '-0.00909', '-0.1263', '-0.01617', '-0.09546', '0.05298', '-0.1388', '-0.00867', '-0.02025', '-0.03357', '-0.0754', '-0.10474', '0.151', '-0.0323', '0.0554', '-0.07574', '-0.0753', '0.0911', '-0.02621', '-0.1316', '-0.002567', '0.1736', '-0.001323', '-0.1991', '-0.0282', '0.09784', '0.0523', '-0.03595', '0.03143', '0.02542', '-0.0464', '0.2476', '0.1455', '-0.0958', '0.188', '-0.1461', '-0.0283', '0.02916', '-0.089', '0.02238', '-0.0528', '0.0646', '-0.0405', '-0.01166', '-0.0233', '-0.005123', '-0.005386', '-0.04263', '0.1218', '-0.014786', '-0.0378', '0.04706', '0.2034', '0.07416', '0.05133', '0.1777', '0.1423', '0.05212', '0.08344', '0.2141', '0.0371', '0.1659', '-0.2096', '0.0694', '0.0721']",,,C563781,,,,
mondo:0012209,branchiogenic deafness syndrome,"['BRANCHIOGENIC-deafness syndrome', 'MC)garbanC)-Loiselet syndrome', 'Mégarbané-Loiselet syndrome']",,609166,50815,C1836673,,,,C563780,,,,
mondo:0012210,"migraine with aura, susceptibility to, 7","['migraine with aura, susceptibility to, 7', 'migraine with aura, susceptibility to, type 7', 'Mgr7']",,609179,,C1836670,,,,,,,,
mondo:0012211,MPDU1-congenital disorder of glycosylation,"['carbohydrate-deficient glycoprotein syndrome type 1F', 'CDG If', 'CDG syndrome type If', 'CDG-If', 'carbohydrate deficient glycoprotein syndrome type If', 'CDG1F', 'congenital disorder of glycosylation type 1f', 'CDG 1F', 'congenital disorder of glycosylation type If', 'MPDU1-CDG', 'MPDU1-CDG (CDG-If)', 'CDGIf', 'congenital disorder of glycosylation, type If']",0080558,609180,79323,C1836669,"['-0.1598', '0.0733', '0.1877', '-0.1138', '0.3389', '-0.3906', '-0.2402', '0.3706', '-0.2795', '-0.1864', '-0.1652', '-0.256', '0.1132', '-0.2588', '-0.0689', '0.2036', '-0.03726', '-0.0404', '-0.2627', '-0.4504', '0.1989', '0.04416', '0.3525', '-0.255', '0.2063', '0.00839', '-0.3198', '-0.2253', '0.198', '-0.3577', '0.2795', '0.356', '0.3347', '0.0906', '-0.2527', '-0.10205', '0.001763', '-0.2327', '-0.4727', '-0.1716', '0.0738', '-0.407', '-0.1168', '-0.01825', '-0.081', '-0.3079', '0.0003448', '0.1863', '0.2498', '0.08545', '-0.2365', '0.2157', '0.05273', '0.0775', '-0.2886', '-0.6226', '0.1755', '0.2032', '-0.4197', '0.42', '0.3652', '-0.001314', '0.541', '0.01012', '0.07745', '-0.1576', '0.02016', '0.1453', '-0.7275', '-0.06384', '-0.4368', '0.2625', '-0.07025', '0.1451', '0.1766', '0.2688', '0.1919', '0.04816', '-0.0903', '0.221', '0.2568', '0.1461', '-0.1349', '0.1451', '0.09937', '-0.2421', '0.386', '0.509', '0.0698', '0.0901', '0.1516', '0.362', '-0.02834', '-0.2047', '0.408', '0.4502', '0.4272', '-0.4626', '0.1186', '0.2468']",C126872,,C535744,,,,
mondo:0012212,Loeys-Dietz syndrome 1,"['TGFBR1 Loeys-Dietz syndrome', 'Loeys-Dietz syndrome caused by mutation in TGFBR1', 'Loeys-Dietz aortic aneurysm syndrome', 'Loeys-Dietz syndrome 1', 'LDS1', 'Furlong syndrome', 'Loeys-Dietz syndrome type 1', 'aortic aneurysm, familial thoracic 5']",0070235,609192,97295,C2697933,,C75119,,,,,,
mondo:0012213,hereditary spastic paraplegia 26,"['autosomal recessive spastic paraplegia type 26', 'SPG26', 'spastic paraplegia 26', 'GM2 synthase deficiency', 'spastic paraplegia 26, autosomal recessive', 'hereditary spastic paraplegia type 26', 'autosomal recessive spastic paraplegia 26']",0110777,609195,101006,C4511959,"['-0.04617', '0.09753', '0.382', '-0.4712', '-0.067', '-0.7754', '-0.06216', '0.504', '-1.099', '-0.1959', '-0.4072', '0.2542', '-0.499', '-0.2029', '0.2372', '-0.10315', '0.2288', '-0.7324', '-0.2338', '-0.1498', '-0.1823', '-0.13', '-0.5117', '0.07153', '0.173', '0.2886', '-0.1927', '-0.2063', '0.3857', '-0.0748', '-0.2566', '0.365', '0.831', '0.1825', '0.2622', '-0.4673', '-0.3457', '-0.3945', '-0.4653', '-0.1356', '0.3542', '-0.685', '0.3665', '0.699', '0.325', '-0.7637', '-0.168', '0.2742', '0.3792', '0.098', '-0.2092', '0.9697', '-0.754', '-0.5425', '0.1866', '0.197', '0.7715', '-0.1893', '-0.4285', '0.461', '0.3738', '0.4663', '0.593', '0.442', '-0.601', '0.0932', '-0.1611', '0.405', '-0.361', '0.1464', '-0.3135', '0.536', '0.01423', '-0.1973', '0.7827', '0.1019', '0.02036', '0.181', '-0.1992', '0.10394', '0.1305', '-0.3428', '0.1832', '0.4326', '0.2305', '0.301', '0.1438', '0.828', '0.8174', '0.04453', '-0.02817', '0.564', '0.0981', '-0.3203', '0.9175', '0.4944', '0.8804', '-0.07623', '0.083', '0.0238']",,,C536862,,,,
mondo:0012214,glucocorticoid deficiency 3,"['glucocorticoid deficiency 3', 'familial glucocorticoid deficiency 3', 'glucocorticoid deficiency 2', 'GCCD3', 'glucocorticoid deficiency 2, formerly']",,609197,,C1836621,,,,C563776,,,,
mondo:0012215,myofibrillar myopathy 3,"['myotilinopathy', 'MYOT autosomal dominant limb-girdle muscular dystrophy', 'MFM3', 'LGMD1', 'muscular dystrophy, limb-girdle, type 1A', 'muscular dystrophy limb-girdle type 1A', 'distal myotilinopathy', 'spheroid body myopathy', 'LGMD1A', 'autosomal dominant distal myopathy caused by mutation in MYOT', 'muscular dystrophy, proximal, type 1A', 'myopathy, spheroid body', 'myofibrillar myopathy type 3', 'autosomal dominant spheroid body myopathy', 'autosomal dominant limb-girdle muscular dystrophy type 1A', 'limb-girdle muscular dystrophy due to myotilin deficiency', 'MYOT autosomal dominant distal myopathy', 'myopathy, myofibrillar, 3', 'proximal muscular dystrophy type 1A', 'myopathy, myofibrillar, type 3', 'limb-girdle muscular dystrophy type 1A', 'myopathy, myofibrillar, myotilin-related', 'autosomal dominant limb-girdle muscular dystrophy caused by mutation in MYOT']",0110300,609200,98911,C1866785,"['-0.8994', '0.316', '0.01927', '-0.02518', '0.337', '-0.354', '-0.0619', '0.1466', '-0.503', '0.10266', '-0.3418', '0.193', '0.2195', '0.3162', '0.12067', '0.09985', '-0.4028', '-0.2522', '-0.2062', '-0.8228', '0.3792', '-0.00553', '0.5425', '0.1368', '0.0906', '-0.03084', '-0.0805', '-0.1918', '-0.5586', '0.03204', '0.4949', '0.1523', '0.07074', '0.3186', '0.02127', '-0.116', '-0.534', '0.2754', '0.0502', '-0.4885', '-0.1681', '-0.2617', '-0.2186', '0.3958', '-0.325', '0.08105', '-0.2737', '-0.01735', '0.04712', '0.2576', '-0.0795', '0.09576', '0.1578', '0.05756', '0.1602', '-0.6875', '0.54', '-0.5923', '-0.3994', '-0.1189', '0.2168', '0.0588', '0.00775', '0.08044', '-0.685', '0.293', '0.4114', '0.741', '-0.3933', '-0.0069', '-0.1549', '0.0928', '0.109', '0.11475', '0.2103', '0.0997', '-0.0824', '0.46', '-0.02475', '-0.598', '-0.09125', '-0.0416', '0.618', '0.2537', '-0.05353', '0.4368', '-0.4348', '0.1981', '0.1503', '-0.2612', '0.4124', '0.1982', '0.03818', '0.07196', '0.2695', '0.2065', '0.687', '-0.1175', '-0.06177', '0.3442']",,,C563775,,,,
mondo:0012216,foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome,"['foveal hypoplasia type 2', 'foveal hypoplasia 2, with or without optic nerve misrouting and/or anterior segment dysgenesis', 'foveal hypoplasia 2 with optic nerve decussation defects and anterior segment dysgenesis without albinism', 'foveal hypoplasia 2 with or without optic nerve misrouting and/or anterior segment dysgenesis', 'foveal hypoplasia 2', 'FVH2', 'FHONDA syndrome']",,609218,397618,,"['-0.597', '0.1062', '0.2698', '0.01036', '0.1879', '0.10034', '-0.0842', '0.0846', '-0.2043', '-0.1947', '-0.08795', '-0.3704', '-0.2161', '-0.2313', '-0.2167', '-0.4045', '0.339', '-0.1245', '0.2588', '-0.701', '-0.01223', '-0.1013', '0.0362', '-0.05978', '0.1439', '0.1946', '-0.2161', '0.2283', '0.2412', '0.2566', '0.328', '0.1412', '0.3787', '0.2808', '0.0971', '-0.03705', '0.2297', '-0.2499', '-0.01295', '-0.515', '0.3142', '-0.012566', '0.0842', '-0.1058', '-0.2423', '-0.2048', '0.2346', '0.0269', '0.3098', '-0.0931', '0.01982', '0.03714', '-0.2244', '-0.282', '-0.10114', '0.08466', '0.714', '0.03665', '-0.4465', '-0.0804', '0.05237', '-0.0334', '0.003662', '0.4248', '-0.2205', '-0.0593', '0.4727', '0.532', '-0.1294', '0.4258', '-0.2842', '0.356', '0.1059', '-0.124', '0.1431', '-0.2688', '0.227', '-0.2495', '-0.3381', '-0.2013', '0.2263', '0.06183', '0.0602', '0.7554', '-0.5024', '-0.3489', '0.06226', '0.423', '0.11584', '0.10504', '0.1681', '0.332', '0.0582', '-0.02145', '0.7217', '-0.1815', '0.2267', '-0.012764', '0.004128', '0.3115']",,,C563774,,,,
mondo:0012217,Bruck syndrome 2,"['Bruck syndrome 2', 'BRKS2', 'Bruck syndrome type 2', 'PLOD2 Bruck syndrome', 'Bruck syndrome caused by mutation in PLOD2', 'osteogenesis imperfecta with congenital Joint contractures']",,609220,,C1836602,,,,C537407,,,,
mondo:0012218,"dandy-walker malformation with occipital cephalocele, autosomal dominant","['ADDWOC', 'Dandy-Walker malformation with occipital cephalocele, autosomal dominant']",,609222,,C2674987,,,,C567185,,,,
mondo:0012219,"spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type","['spondyloepiphyseal dysplasia tarda, autosomal recessive, Leroy-Spranger type']",0112291,609223,,C1836584,,,,C563772,,,,
mondo:0012220,Griscelli syndrome type 3,"['Griscelli-Pruni��ras syndrome type 3', 'Griscelli-PruniC)ras syndrome type 3', 'GS3', 'Griscelli syndrome, type 3', 'Griscelli-Pruniéras syndrome type 3', 'hypomelanosis with no immunologic or neurologic manifestations', 'Griscelli disease type 3']",0060834,609227,79478,C1836573,"['-0.261', '0.0968', '0.03165', '0.09106', '0.6934', '-0.256', '-0.42', '0.0944', '-0.283', '-0.05075', '0.04065', '-0.1512', '-0.12006', '-0.1829', '-0.11816', '-0.11346', '0.3113', '0.03812', '-0.2145', '-0.4958', '-0.103', '-0.166', '0.226', '-0.1282', '-0.05725', '0.01831', '-0.1114', '0.07556', '0.02477', '0.006428', '0.4016', '0.01452', '-0.00306', '-0.01913', '0.02174', '0.11707', '-0.1365', '0.01646', '-0.08704', '-0.3071', '0.528', '-0.523', '-0.06445', '-0.3', '-0.3718', '-0.3923', '0.2422', '0.1407', '0.437', '-0.0779', '-0.1595', '-0.275', '0.221', '0.0851', '-0.12494', '-0.237', '0.33', '0.2081', '-0.4146', '-0.1904', '-0.1238', '-0.04633', '0.309', '-0.1843', '0.10315', '0.2329', '0.324', '0.0802', '-0.341', '0.3464', '-0.3389', '-0.3164', '-0.1622', '0.02136', '0.1049', '0.0246', '0.0458', '-0.00988', '-0.1266', '-0.1625', '0.3398', '-0.3005', '-0.098', '0.06256', '-0.1095', '-0.302', '0.1946', '0.5054', '0.1506', '0.1918', '0.2299', '0.2124', '-0.0618', '-0.1287', '0.5303', '0.1661', '-0.001982', '-0.346', '0.03568', '0.3113']",,,C537303,,E70.3,,
mondo:0012221,alpha-N-acetylgalactosaminidase deficiency type 1,"['N-acetyl-alpha-D-galactosaminidase deficiency type III', 'Schindler disease, type III', 'Alpha-N-acetylgalactosaminidase deficiency, type 3', 'Schindler disease, type 3', 'NAGA deficiency, type 1', 'Schindler disease, type I', 'NAGA deficiency type 1', 'neuroaxonal dystrophy, Schindler type', 'Schindler disease, type 1', 'Schindler disease type 1', 'Schindler disease type I', 'NAGA deficiency, type 3', 'alpha-N-acetylgalactosaminidase deficiency, type 1', 'Alpha-N-acetylgalactosaminidase deficiency, type 1']",0112318,609241,79281,C1836545,"['0.0716', '0.1434', '0.0963', '0.3833', '0.363', '-0.796', '0.3545', '0.5093', '-0.4397', '-0.2114', '-0.06616', '-0.06903', '-0.619', '-0.5396', '0.3171', '-0.0766', '0.859', '-0.1183', '-0.1979', '-0.5044', '-0.3406', '-0.59', '-0.0993', '-0.02591', '-0.521', '0.03622', '-0.2218', '-0.03998', '-0.2605', '0.2473', '0.507', '0.3125', '0.4575', '0.349', '-0.02705', '0.1793', '-0.2678', '-0.2441', '-0.1687', '0.1876', '0.1628', '-0.65', '0.036', '0.2418', '0.0981', '0.1188', '0.1798', '0.3884', '-0.2251', '0.0163', '0.1733', '0.03738', '-0.174', '-0.205', '-0.1342', '-0.01479', '0.1506', '-0.3916', '-0.3042', '0.4355', '-0.1917', '-0.2876', '0.3606', '-0.1302', '-0.4207', '-0.3008', '0.465', '0.3274', '-0.783', '0.2886', '-0.1267', '0.10065', '-0.0702', '-0.3008', '0.6685', '0.2966', '-0.01222', '-0.4902', '-0.2756', '-0.0914', '0.4788', '0.09546', '-0.367', '0.3794', '0.418', '0.00915', '-0.12225', '0.578', '0.548', '0.328', '0.609', '0.549', '0.2367', '-0.01833', '0.3613', '0.33', '0.513', '-0.3416', '0.401', '0.006016']",,,,,,,
mondo:0012222,alpha-N-acetylgalactosaminidase deficiency type 2,"['KANZAKI disease', 'Alpha-N-acetylgalactosaminidase deficiency adult onset', 'Alpha-N-acetylgalactosaminidase deficiency, adult-onset', 'Kanzaki disease', 'Schindler disease, type 2', 'adult-onset Alpha-N-acetylgalactosaminidase deficiency', 'NAGA deficiency type 2', 'Naga deficiency, type 2', 'Schindler disease type 2', 'Alpha-N-acetylgalactosaminidase deficiency, type 2']",0112319,609242,79280,C1836522,"['-0.422', '0.0343', '0.3823', '0.194', '-0.1488', '-0.2593', '0.2896', '0.2312', '-0.069', '0.1708', '0.03876', '-0.2484', '0.01103', '-0.4978', '-0.1669', '0.0753', '0.06604', '-0.07556', '-0.2368', '-0.2004', '0.1816', '-0.3254', '0.161', '0.4304', '-0.0724', '0.02902', '-0.2554', '-0.01353', '0.1409', '0.0502', '0.5513', '0.4688', '0.2245', '0.2834', '0.275', '-0.0331', '-0.4053', '0.107', '0.1357', '-0.2632', '0.26', '-0.819', '-0.06946', '-0.1274', '-0.01276', '0.2034', '0.1181', '0.3184', '-0.02774', '-0.3828', '0.3936', '0.4983', '-0.0695', '0.3333', '-0.59', '-0.1469', '0.02783', '-0.961', '0.07196', '0.296', '0.1109', '-0.3562', '-0.11285', '-0.2834', '-0.36', '-0.3982', '-0.12384', '0.5103', '-0.4016', '0.4333', '0.00693', '-0.03111', '0.1736', '-0.1852', '0.0727', '0.4792', '-0.04727', '0.245', '-0.1064', '0.03406', '-0.1087', '-0.4307', '-0.152', '0.5854', '-0.1103', '-0.242', '-0.2778', '-0.12384', '0.243', '-0.1958', '0.8667', '0.4937', '0.5728', '-0.003489', '1.491', '0.2793', '-0.2542', '-0.3555', '0.1655', '0.6836']",,,,,,,
mondo:0012223,"hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate","['Marie Unna-like scalp hypotrichosis', 'hypotrichosis, progressive patterned scalp, with wiry hair, onycholysis, and cleft lip/palate']",,609250,,C1836521,,,,C563765,,,,
mondo:0012224,"febrile seizures, familial, 6","['FEB6', 'convulsions, familial febrile, 6', 'febrile seizures, familial, 6']",0111309,609253,,C1836518,,,,C563764,,,,
mondo:0012225,Senior-Loken syndrome 5,"['SLSN5', 'Senior-Loken syndrome caused by mutation in IQCB1', 'Senior-Loken syndrome 5', 'SENIOR-Loken syndrome 5', 'IQCB1 Senior-Loken syndrome', 'Senior-Loken syndrome type 5']",,609254,,C1836517,,,,C563763,,,,
mondo:0012226,"febrile seizures, familial, 5","['FEB5', 'convulsions, familial febrile, 5', 'febrile seizures, familial, 5']",0111306,609255,,C1836507,,,,C563762,,,,
mondo:0012227,myopia 7,"['myopia 7', 'MYP7']",,609256,,C1836506,,,,C563761,,,,
mondo:0012228,myopia 8,"['myopia 8', 'MYP8']",,609257,,C1836505,,,,C563760,,,,
mondo:0012229,myopia 9,"['myopia 9', 'MYP9']",,609258,,C1836504,,,,C563759,,,,
mondo:0012230,myopia 10,"['myopia 10', 'MYP10']",,609259,,C1836503,,,,C563758,,,,
mondo:0012231,Charcot-Marie-Tooth disease type 2A2,"['Charcot-Marie-Tooth neuropathy type 2A2', 'Charcot-Marie-Tooth disease type 2 caused by mutation in MFN2', 'Charcot-Marie-Tooth disease, neuronal, type 2A2', 'Charcot-Marie-Tooth neuronal type 2A2', 'CMT2A2', 'Charcot-Marie-Tooth neuropathy, type 2A2', 'MFN2 Charcot-Marie-Tooth disease type 2', 'hereditary motor and sensory neuropathy IIA2', 'HMSN IIA2', 'HMSN2A2', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2A2', 'HMSN IIa2', 'autosomal dominant Charcot-Marie-Tooth disease type 2A2', 'Charcot-Marie-Tooth disease, axonal, type 2A2A', 'CMT2A2A', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2A2', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2A2A', 'Charcot-Marie-Tooth disease, axonal, type 2A2', 'hereditary motor and sensory neuropathy IIa2', 'Charcot-Marie-Tooth disease type 2A2A']",0110155,609260,99947,C1836485,"['0.3823', '0.439', '0.0966', '-0.3032', '0.01683', '-0.5605', '0.02628', '1.081', '-0.5615', '-0.6187', '0.04663', '0.0337', '-0.969', '0.367', '-0.177', '-0.4773', '-0.2192', '-0.7637', '-0.5728', '-0.416', '0.0005026', '-0.2028', '0.01096', '0.6455', '0.1564', '0.494', '0.2227', '0.225', '-0.1254', '0.02888', '-0.3384', '-0.528', '0.022', '-0.0952', '0.3037', '-0.7236', '-0.4583', '-0.5356', '0.514', '0.1826', '-1.142', '-0.271', '-0.3752', '0.2316', '-0.2603', '-0.1412', '0.1876', '0.01944', '-0.0709', '-0.2642', '-0.00747', '0.271', '-0.4011', '-1.097', '0.36', '0.1296', '-0.2089', '0.4563', '-0.305', '-0.1978', '-0.3972', '0.1613', '0.265', '0.5864', '-0.687', '1.026', '-0.2847', '0.6787', '-0.8154', '0.502', '-0.8784', '0.2673', '0.105', '-0.3066', '1.077', '0.6567', '-0.2783', '0.3162', '-0.1348', '-0.783', '-0.1323', '-0.09814', '0.762', '0.748', '-0.2537', '0.4014', '0.1642', '1.04', '0.7876', '0.2632', '0.1918', '-0.3035', '0.2917', '0.3257', '0.47', '0.4207', '0.912', '-0.311', '-0.01152', '0.5977']",C150646,,C563757,,,,
mondo:0012232,"stuttering, familial persistent, 2","['stuttering, familial persistent, 2', 'STUT2']",,609261,,C1836484,,,,C563756,,,,
mondo:0012235,autosomal recessive spinocerebellar ataxia 7,"['spinocerebellar ataxia autosomal recessive 7', 'childhood-onset autosomal recessive slowly progressive spinocerebellar ataxia', 'SCAR7', 'spinocerebellar ataxia, autosomal recessive 7', 'autosomal recessive spinocerebellar ataxia type 7', 'spinocerebellar ataxia, autosomal recessive type 7', 'childhood onset autosomal recessive slowly progressive spinocerebellar ataxia']",0080059,609270,284324,C1836474,"['-0.1927', '-0.2247', '0.0293', '-0.11206', '-0.1131', '-0.9185', '0.0828', '0.07556', '-0.6855', '-0.868', '0.1359', '0.2338', '-0.1526', '0.1432', '0.443', '-0.3027', '-0.2668', '-0.3154', '0.08136', '-0.777', '-0.1024', '-0.1997', '0.0522', '-0.462', '0.6216', '-0.4585', '-0.3525', '0.1559', '-0.1597', '-0.6475', '0.09424', '0.2607', '-0.4585', '-0.1543', '0.3186', '0.1919', '-0.2158', '-0.01148', '0.541', '0.2944', '0.3137', '0.1137', '-0.4128', '0.3872', '0.4338', '-0.4763', '0.208', '0.2874', '0.2231', '-0.0345', '-0.2007', '0.1215', '-0.11414', '-0.4138', '-0.06146', '-0.76', '0.25', '0.4421', '-0.175', '0.4316', '-0.5127', '0.295', '0.2347', '-0.1593', '-0.566', '0.551', '0.3416', '0.5044', '-0.4695', '0.4993', '0.894', '0.4727', '-0.1125', '-0.646', '0.642', '0.344', '0.2369', '0.2754', '0.1504', '0.324', '-0.4023', '-0.7183', '0.4614', '0.6206', '-0.3706', '-0.607', '0.2522', '-0.1185', '0.518', '0.4487', '0.334', '0.4485', '-0.01426', '0.04962', '1.013', '1.128', '0.4365', '0.527', '-0.2683', '0.0425']",,,C563753,,,,
mondo:0012236,keratoconus 4,"['keratoconus 4', 'KTCN4']",,609271,,C1836473,,,,C563752,,,,
mondo:0012237,nemaline myopathy 6,"['nemaline myopathy caused by mutation in KBTBD13', 'KBTBD13 nemaline myopathy', 'NEM6', 'nemaline myopathy 6, autosomal dominant', 'nemaline myopathy type 6', 'nemaline myopathy 6']",0110935,609273,,C1836472,,,,C538398,,,,
mondo:0012238,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2","['progressive external ophthalmoplegia, autosomal dominant 2', 'PEOA2', 'SLC25A4 progressive external ophthalmoplegia with mitochondrial DNA deletions', 'progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in SLC25A4', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 2']",0111517,609283,,C1836460,,,,C563750,,,,
mondo:0012239,"congenital myopathy 4B, autosomal recessive","['nemaline myopathy 1, autosomal dominant or recessive', 'Nem1', 'nemaline myopathy type 1', 'nemaline myopathy caused by mutation in TPM3', 'TPM3 nemaline myopathy', 'nemaline myopathy 1', 'NEM1']",0110926,609284,171881,C1836448,,,,C538348,,,,
mondo:0012240,nemaline myopathy 4,"['TPM2 nemaline myopathy', 'nemaline myopathy 4, autosomal dominant', 'nemaline myopathy 4', 'nemaline myopathy type 4', 'NEM4', 'nemaline myopathy caused by mutation in TPM2', 'Cap myopathy 2']",0110932,609285,171881,C1836447,"['-0.3374', '0.0926', '-0.0834', '-0.1372', '-0.11926', '-0.56', '0.1147', '0.3088', '-0.4883', '-0.38', '-0.07495', '0.2109', '0.04642', '0.347', '-0.0518', '-0.01622', '-0.1107', '-0.06976', '-0.04953', '-0.7017', '0.0357', '0.05826', '0.267', '-0.01675', '0.07056', '-0.1553', '0.1919', '-0.1145', '-0.1299', '0.1438', '0.014114', '0.03763', '0.0007973', '0.2', '-0.1301', '-0.2993', '0.08545', '-0.0996', '0.09033', '0.02263', '-0.1711', '-0.3577', '-0.010124', '0.2578', '-0.07086', '-0.0764', '-0.2242', '0.3035', '0.05173', '-0.0559', '-0.2295', '0.03162', '0.1682', '-0.3604', '-0.1431', '-0.5176', '0.1466', '-0.10376', '0.2212', '-0.1305', '0.2255', '-0.007095', '-0.2246', '0.001816', '-0.1813', '0.02788', '0.2471', '0.626', '-0.263', '0.2153', '-0.1455', '-0.01333', '0.1003', '-0.032', '0.3254', '0.04526', '-0.3186', '-0.0688', '0.1223', '-0.1956', '-0.1273', '0.03848', '0.1221', '0.2698', '-0.0754', '0.1214', '-0.1357', '0.1833', '0.4011', '0.05362', '0.4065', '0.04456', '0.0491', '0.2174', '0.3025', '0.2607', '0.445', '-0.11346', '-0.004116', '0.04233']",C164225,,C538351,,,,
mondo:0012241,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3","['progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 3', 'progressive external ophthalmoplegia, autosomal dominant 3', 'progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in TWNK', 'PEOA3', 'TWNK progressive external ophthalmoplegia with mitochondrial DNA deletions', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 3']",0111520,609286,,C1836439,,,,C563747,,,,
mondo:0012242,"syncope, familial vasovagal","['syncope, familial VASOVAGAL', 'syncope, familial Neurocardiogenic', 'VVS', 'syncope familial neurocardiogenic', 'familial vasovagal syncope', 'familial neurocardiogenic syncope']",,609289,,C1836438,,,,C536849,,,,
mondo:0012243,"B-cell immunodeficiency, distal limb anomalies, and urogenital malformations","['Hoffman syndrome', 'B-cell immunodeficiency, distal limb anomalies, and urogenital malformations', 'Bilu syndrome']",,609296,,C1836437,,,,C563745,,,,
mondo:0012244,"prostate cancer, hereditary, 5","['prostate cancer, hereditary, type 5', 'HPC5', 'prostate cancer, hereditary, 5']",,609299,,C1836436,,,,C563744,,,,
mondo:0012245,"developmental and epileptic encephalopathy, 3","['epileptic encephalopathy, early infantile, type 3', 'developmental and epileptic encephalopathy 3', 'DEE3', 'early infantile epileptic encephalopathy caused by mutation in SLC25A22', 'SLC25A22 early infantile epileptic encephalopathy', 'EIEE3', 'epileptic encephalopathy, early infantile, 3']",0080440,609304,,,,,,,,,,
mondo:0012246,spinocerebellar ataxia type 26,"['spinocerebellar ataxia type 26', 'SCA26', 'spinocerebellar ataxia 26']",0050975,609306,101112,C1836395,"['-0.1014', '-0.2397', '-0.2025', '0.1901', '-0.05417', '-0.7207', '0.1743', '0.293', '-0.6323', '-0.876', '-0.04565', '0.2937', '-0.1348', '0.04916', '0.5693', '-0.4307', '-0.1098', '-0.4045', '0.1892', '-0.845', '-0.2878', '-0.2081', '0.08356', '-0.7085', '0.2323', '-0.4998', '-0.2534', '0.2332', '0.02458', '-0.981', '0.0244', '0.4214', '-0.2463', '-0.1787', '0.399', '-0.0765', '0.0849', '0.237', '0.4954', '0.4207', '0.2534', '0.047', '-0.2776', '0.5605', '0.6313', '-0.6577', '-0.05734', '0.2174', '0.3118', '-0.1825', '-0.2395', '0.2166', '-0.1268', '-0.4453', '-0.014', '-0.7666', '0.2037', '0.4626', '-0.1554', '0.6396', '-0.5576', '0.3726', '0.2311', '0.089', '-0.525', '0.325', '0.1809', '0.4673', '-0.692', '0.3667', '0.615', '0.454', '-0.09454', '-0.7515', '0.763', '0.4685', '0.1815', '0.1407', '0.04044', '0.597', '-0.2072', '-0.9126', '0.3293', '0.6743', '-0.357', '-0.759', '0.2966', '0.2365', '0.49', '0.267', '0.347', '0.3635', '0.1881', '0.01128', '0.97', '0.967', '0.4531', '0.4265', '-0.1937', '0.06244']",,,C537203,,,,
mondo:0012247,spinocerebellar ataxia type 27,"['SCA27', 'cerebellar ataxia autosomal dominant FGF14-related', 'spinocerebellar ataxia type 27', 'cerebellar ataxia, autosomal dominant, Fgf14-related', 'spinocerebellar ataxia 27']",0050976,609307,98764,C4304846,"['-0.079', '-0.165', '0.00619', '0.0811', '-0.3147', '-0.982', '0.3047', '0.1782', '-0.7695', '-0.967', '0.12445', '0.1274', '-0.1543', '0.1908', '0.739', '-0.46', '-0.02553', '-0.3503', '0.11957', '-0.957', '-0.0768', '-0.3025', '0.1849', '-0.6665', '0.501', '-0.5464', '-0.3145', '0.1547', '-0.209', '-0.9062', '0.01982', '0.567', '-0.521', '-0.2322', '0.3906', '0.149', '-0.2213', '0.1797', '0.5513', '0.589', '0.3804', '0.15', '-0.5166', '0.2664', '0.5093', '-0.665', '0.1097', '0.4773', '0.4438', '-0.0854', '-0.11115', '0.09534', '-0.18', '-0.3877', '-0.05826', '-0.7363', '0.2654', '0.4587', '0.06216', '0.5664', '-0.5605', '0.2686', '0.2361', '-0.196', '-0.4817', '0.426', '0.1295', '0.4412', '-0.581', '0.371', '0.7627', '0.404', '0.0442', '-0.753', '0.75', '0.502', '0.01453', '0.1377', '0.1812', '0.5645', '-0.3936', '-0.954', '0.391', '0.6216', '-0.2783', '-0.711', '0.1362', '0.06415', '0.595', '0.4573', '0.2876', '0.546', '-0.04486', '0.04932', '1.137', '1.13', '0.4646', '0.3801', '-0.2279', '-0.2151']",,,C537204,,,,
mondo:0012248,autosomal recessive limb-girdle muscular dystrophy type 2K,"['LGMD2K', 'limb-girdle muscular dystrophy-intellectual disability syndrome', 'LGMD-POMT1 related', 'muscular dystrophy-dystroglycanopathy (limb-girdle) type C 1', 'muscular dystrophy-dystroglycanopathy (Limb-girdle) type C, 1', 'MDDGC1', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 1', 'muscular dystrophy limb-girdle type 2K', 'POMT1 autosomal recessive limb-girdle muscular dystrophy', 'limb-girdle muscular dystrophy - intellectual disability', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT1', 'muscular dystrophy, limb-girdle, type 2K', 'limb-girdle muscular dystrophy type 2K']",0110297,609308,86812,,"['0.0915', '-0.591', '-0.3523', '-0.4065', '0.6167', '-1.032', '0.1786', '1.065', '-1.809', '-0.708', '-0.1547', '0.5815', '-0.291', '0.77', '0.2272', '0.245', '-0.9424', '-0.6514', '-0.5093', '-0.509', '0.1256', '0.2482', '0.1293', '0.49', '-0.0375', '-0.003952', '-0.00617', '-0.8047', '0.1404', '-0.2335', '0.6367', '-0.3616', '0.646', '0.3052', '0.10986', '0.258', '-0.683', '0.2976', '0.05133', '-0.294', '0.2296', '-0.3604', '-0.619', '0.1307', '-0.2188', '0.1398', '0.2766', '0.6313', '-0.3271', '0.403', '0.2471', '-0.2256', '0.3608', '-0.645', '0.4268', '-0.664', '0.356', '0.77', '-0.064', '0.2081', '0.1001', '-0.2185', '-0.1434', '-0.2925', '-0.02223', '0.02286', '-0.12036', '0.3506', '-0.6646', '-0.2585', '-0.201', '0.504', '-0.0473', '-0.1118', '0.8438', '0.6733', '0.2217', '0.4006', '-0.06335', '0.186', '0.1294', '-0.02303', '-0.0206', '0.1605', '0.02199', '-0.04276', '-0.2852', '-0.1981', '0.6963', '0.3357', '-0.3018', '0.427', '0.1012', '1.037', '0.0808', '0.1783', '0.3914', '-0.5205', '0.1455', '-0.149']",C133730,0009145,,,,,
mondo:0012249,Lynch syndrome 2,"['colorectal cancer, hereditary nonpolyposis, type 2', 'Hereditary nonpolyposis colorectal cancer type 2', 'colon cancer, familial nonpolyposis, type 2', 'Lynch 2 syndrome', 'COCA2', 'familial non-polyposis colon cancer type 2', 'Hereditary non-polyposis colon cancer type 2', 'HNPCC2']",0070274,609310,,,,C6726,,D055847,,,,
mondo:0012250,Charcot-Marie-Tooth disease type 4H,"['CMT4H', 'Charcot-Marie-Tooth neuropathy type 4H', 'autosomal recessive Charcot-Marie-Tooth disease type 4H', 'Charcot-Marie-Tooth neuropathy, type 4H', 'autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4H', 'Charcot-Marie-Tooth disease type 4 caused by mutation in FGD4', 'FGD4 Charcot-Marie-Tooth disease type 4', 'Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4H', 'Charcot-Marie-Tooth disease, type 4H', 'Charcot-Marie-Tooth disease, autosomal recessive, type 4H']",0110192,609311,99954,C1836336,"['0.1943', '0.3633', '0.2966', '-0.0157', '0.1294', '-0.05972', '-0.2013', '0.4749', '-0.967', '-0.02194', '0.0941', '0.2961', '-0.3003', '-0.1625', '-0.08875', '-0.483', '-0.01414', '-0.3853', '-0.4016', '-0.5977', '0.1172', '0.463', '0.445', '0.3044', '0.2047', '0.599', '0.1453', '0.1343', '0.06323', '-0.2878', '0.05603', '-0.5723', '0.278', '0.185', '0.437', '-0.732', '-0.4058', '-0.0756', '0.311', '-0.3135', '-1.576', '-0.477', '-0.57', '0.6167', '-0.1869', '-0.1439', '0.0212', '0.373', '-0.261', '0.04816', '0.1359', '0.2067', '-0.363', '-0.9717', '0.4175', '-0.3525', '-0.3936', '0.1936', '-0.623', '0.1803', '-0.3418', '0.1608', '0.6787', '0.757', '-0.974', '0.932', '0.136', '0.7456', '-0.5337', '0.4358', '-0.7085', '0.226', '0.617', '-0.3481', '1.197', '0.2913', '-0.4075', '0.396', '0.1136', '-0.4138', '-0.2566', '0.05103', '0.539', '0.513', '-0.00181', '0.02226', '0.0679', '0.5635', '0.9795', '0.292', '0.039', '-0.0852', '0.4453', '0.53', '0.2676', '0.464', '0.634', '-0.4834', '-0.06604', '0.272']",,,C563740,,,,
mondo:0012251,MEDNIK syndrome,"['mental retardation, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma', 'erythrokeratodermia variabilis, Kamouraska type', 'erythrokeratodermia variabilis 3', 'mental retardation, enteropathy, deafness, neuropathy, ichthyosis, keratodermia', 'intellectual disability, enteropathy, deafness, neuropathy, ichthyosis, keratodermia', 'intellectual disability, enteropathy, deafness, peripheral neuropathy, ichthyosis, and keratoderma', 'MEDNIK', 'intellectual disability-enteropathy-deafness-peripheral neuropathy-ichthyosis-keratodermia syndrome']",0060483,609313,171851,CN229776,"['0.02481', '0.4043', '0.5435', '0.3423', '0.361', '-0.8433', '-0.3257', '0.2443', '0.1927', '0.1147', '0.003332', '-0.26', '-0.2499', '-0.284', '0.1868', '0.0327', '-0.0835', '-0.1268', '0.3174', '-0.2573', '0.2399', '-0.2251', '-0.1537', '-0.4004', '0.2032', '0.3103', '-0.6357', '-0.0537', '-0.0985', '-0.492', '0.084', '-0.159', '-0.11', '0.1142', '-0.1111', '-0.706', '0.0539', '-0.557', '-0.2122', '-0.1572', '-0.473', '-0.966', '0.325', '-0.0808', '0.1719', '-0.3704', '0.00952', '0.2156', '-0.1727', '-0.0821', '-0.2935', '0.2161', '-0.2207', '-0.1527', '-0.0643', '-0.3064', '0.5938', '-0.3435', '-0.487', '0.2961', '-0.3042', '-0.1145', '0.3281', '0.3774', '-0.204', '0.0448', '-0.06824', '0.3357', '-0.1926', '0.33', '-0.6553', '0.1328', '0.06165', '-0.3179', '0.1415', '0.3645', '-0.21', '-0.01395', '-0.0962', '0.5117', '0.1357', '-0.1461', '-0.6255', '0.8413', '0.04758', '-0.2925', '0.3713', '1.178', '-0.004753', '0.0922', '0.2732', '0.4783', '0.1813', '-0.3464', '0.87', '-0.1177', '0.2194', '-0.853', '0.4124', '-0.03754']",,,C563739,,,,
mondo:0012252,rhabdoid tumor predisposition syndrome 1,"['At/RT', 'familial rhabdoid tumour caused by mutation in SMARCB1', 'rhabdoid tumor predisposition syndrome type 1', 'SMARCB1 familial rhabdoid tumour', 'brain tumor, posterior fossa, of infancy, familial', 'teratoid tumor, atypical', 'rhabdoid tumour predisposition syndrome type 1', 'SMARCB1 familial rhabdoid tumor', 'rhabdoid tumors, somatic', 'malignant rhabdoid tumor, somatic', 'RTPS1', 'familial rhabdoid tumor caused by mutation in SMARCB1', 'rhabdoid tumor predisposition syndrome 1']",,609322,99966,C1266184,,C178393,,C563738,,,,
mondo:0012253,"multiple epiphyseal dysplasia, with severe proximal femoral dysplasia","['epiphyseal dysplasia, multiple, with severe proximal femoral dysplasia']",,609324,166029,C1836315,,,,C563736,,Q77.3,,
mondo:0012254,"multiple epiphyseal dysplasia, with miniepiphyses","['epiphyseal dysplasia, multiple, with miniepiphyses']",,609325,166032,C1836307,,,,C563735,,Q77.3,,
mondo:0012255,chromosome 18 pericentric inversion,['chromosome 18 pericentric inversion'],,609334,,C1836305,,,,C563734,,,,
mondo:0012256,hereditary spastic paraplegia 28,"['hereditary spastic paraplegia type 28', 'SPG28', 'autosomal recessive pure spastic paraplegia caused by mutation in DDHD1', 'autosomal recessive spastic paraplegia type 28', 'spastic paraplegia 28, autosomal recessive', 'DDHD1 autosomal recessive pure spastic paraplegia', 'autosomal recessive spastic paraplegia 28']",0110779,609340,101008,C1836295,"['-0.19', '0.1726', '-0.004284', '-0.751', '-0.2737', '-0.8105', '-0.6187', '0.4285', '-0.7812', '-0.454', '-0.1765', '0.2434', '-0.5645', '0.1774', '0.1425', '-0.2426', '0.3325', '-0.4937', '0.3276', '-0.497', '-0.2167', '-0.0951', '-0.292', '0.02594', '-0.003601', '0.02623', '-0.06094', '-0.03632', '-0.3635', '-0.1276', '0.01378', '-0.05582', '-0.05075', '0.4585', '0.1654', '-0.4104', '-0.658', '-0.139', '-0.1014', '-0.1963', '0.2544', '-0.341', '-0.255', '0.4473', '-0.08954', '-0.324', '-0.2227', '0.4224', '0.01493', '0.273', '0.073', '0.2573', '-0.622', '-0.2365', '0.2668', '-0.68', '0.485', '-0.2812', '-0.1477', '0.1482', '0.02637', '0.302', '0.3413', '0.1471', '-0.5586', '0.3499', '0.356', '0.838', '-0.5044', '0.24', '-0.0787', '0.606', '0.0982', '-0.577', '0.728', '0.4065', '-0.2961', '0.372', '0.3577', '-0.010925', '0.1328', '-0.3247', '0.72', '0.843', '0.05362', '0.3079', '0.1498', '0.1664', '0.3481', '0.272', '0.2522', '0.3567', '0.2598', '0.10126', '0.945', '0.6304', '0.511', '0.221', '-0.0402', '0.1517']",,,C563732,,,,
mondo:0012257,Cerebrorenodigital syndrome,['CEREBRORENODIGITAL syndrome with limb malformations and triradiate acetabula'],,609345,1396,C1836287,,,,C563731,,,,
mondo:0012258,"epidermolysis bullosa simplex 2E, with migratory circinate erythema","['epidermolysis bullosa simplex 2E, with migratory circinate erythema', 'EBS-migr', 'epidermolysis bullosa simplex with migratory circinate erythema']",,609352,158681,C1836284,"['0.7495', '0.11743', '-0.5693', '-0.1488', '-0.02005', '-0.708', '-0.611', '0.2773', '-0.1965', '-0.857', '0.39', '-0.3425', '-0.8525', '0.0728', '-0.4102', '0.3198', '0.2006', '-0.846', '-0.1647', '-0.8325', '-0.3752', '-0.2467', '0.4854', '0.5664', '0.571', '0.214', '-1.119', '0.7637', '-0.4685', '-0.825', '0.3418', '-0.2554', '-0.559', '-0.2174', '0.1261', '0.2161', '-1.177', '0.0804', '1.254', '-0.4763', '0.2588', '-0.6953', '0.01368', '-0.0948', '0.05063', '-0.3994', '-0.254', '0.03473', '0.5605', '-0.2147', '-0.3557', '-0.809', '0.4985', '-0.1085', '-0.1384', '-0.705', '-0.06946', '1.079', '-0.8643', '-0.458', '-0.1113', '0.298', '-0.0233', '0.2327', '0.95', '0.835', '0.5234', '0.3542', '-0.6924', '0.2253', '-0.11664', '0.07904', '-0.512', '-0.1521', '-0.1505', '-0.03616', '-0.0845', '0.03552', '-0.2263', '-0.1963', '-0.9243', '0.001034', '-0.1931', '-0.1337', '0.1924', '0.2803', '-0.9775', '0.4607', '1.059', '0.283', '-0.4524', '0.4458', '0.07794', '0.6743', '-0.0291', '0.7734', '0.2261', '-0.6763', '0.972', '0.0643']",,,C563730,,,,
mondo:0012259,colloid cysts of third ventricle,"['neuroepithelial cysts of third ventricle', 'colloid cysts of third ventricle']",,609363,,,,,,C535966,,,,
mondo:0012260,cataract 35,"['autosomal recessive congenital nuclear cataract 1', 'CATCN1', 'cataract 35, congenital nuclear', 'CTRCT35', 'cataract, congenital nuclear, autosomal recessive 1', 'cataract type 35', 'cataract 35']",0110261,609376,,C1836272,,,,C563728,,,,
mondo:0012261,"autism, susceptibility to, 6","['AUTS6', 'autism, susceptibility to, 6', 'autism susceptibility 6']",,609378,,C1836271,,,,,,,,
mondo:0012262,"fibrosis of extraocular muscles, congenital, 3c","['fibrosis of extraocular muscles, congenital, 3C', 'Feom4 locus', 'CFEOM3C']",0081019,609384,,C2750404,,,,C567666,,,,
mondo:0012263,"autoimmune disease, susceptibility to, 4","['autoimmune disease, susceptibility to, 4', 'AIS4', 'vitiligo-associated multiple autoimmune disease susceptibility 5', 'autoimmune disease susceptibility locus, chromosome 4-related']",,609400,,,,,,,,,,
mondo:0012264,preeclampsia/eclampsia 2,"['PREECLAMPSIA/eclampsia 2', 'PEE2']",,609402,,C1836257,,,,,,,,
mondo:0012265,preeclampsia/eclampsia 3,"['PEE3', 'PREECLAMPSIA/eclampsia 3']",,609403,,C1836256,,,,,,,,
mondo:0012266,preeclampsia/eclampsia 4,"['PREECLAMPSIA/eclampsia 4', 'preeclampsia caused by mutation in STOX1', 'preeclampsia/eclampsia 4', 'STOX1 preeclampsia', 'Preeclampsia/eclampsia type 4', 'PEE4']",,609404,,C1836255,,,,C563724,,,,
mondo:0012267,holoprosencephaly 8,"['holoprosencephaly type 8', 'HPE8', 'holoprosencephaly 8']",0110879,609408,,C1836254,,,,C563723,,,,
mondo:0012268,AIDS,"['acquired immune deficiency', 'AIDS', 'acquired immunodeficiency syndrome, AIDS', 'acquired immune deficiency syndrome', 'acquired immunodeficiency syndrome', 'acquired immunodeficiency disease', 'AIDS, acquired immunodeficiency syndrome']",635,,,,,C2851,0000765,D000163,,,,
mondo:0012269,chromosome 3q29 microdeletion syndrome,"['3q29 microdeletion syndrome', 'chromosome 3q29 microdeletion syndrome, isolated cases', 'microdeletion 3Q29 syndrome', '3q29 deletion', 'chromosome 3q29 deletion syndrome', '3q subtelomere deletion syndrome', 'monosomy 3q29', '3q29 deletion syndrome', 'monosomy 3qter', '3qter deletion', 'Del(3)(q29)']",0060419,609425,65286,C2674949,,,,C567184,,,,
mondo:0012270,Tukel syndrome,"['fibrosis of extraocular muscles, congenital, with ulnar hand anomalies', 'fibrosis of extraocular muscles, congenital, 4', 'congenital extraocular muscle fibrosis with ulnar hand anomalies', 'Cfeom-U', 'Tukel syndrome']",0081021,609428,,C1836217,,,,C536925,,,,
mondo:0012271,mesoaxial synostotic syndactyly with phalangeal reduction,"['syndactyly type 9', 'syndactyly, type 9', 'syndactyly, Malik-Percin type', 'syndactyly, mesoaxial synostotic, with phalangeal reduction', 'MSSD', 'syndactyly Malik-Percin type', 'syndactyly mesoaxial synostotic with phalangeal reduction']",,609432,157801,C1836206,"['-0.2056', '-0.2091', '0.5244', '0.124', '0.335', '-0.4448', '-0.07214', '0.3022', '-0.354', '-0.797', '-0.4114', '-0.08124', '-0.1943', '0.10297', '-0.128', '-0.223', '0.6104', '-0.2422', '-0.05154', '-0.63', '-0.3242', '0.4214', '0.5703', '-0.464', '0.66', '0.453', '-0.03757', '0.2512', '0.0638', '-0.3062', '0.308', '-0.67', '0.015', '0.2109', '0.4485', '-0.3557', '-0.04913', '-0.2186', '-0.11633', '-0.869', '-0.01839', '-0.6973', '0.3713', '-0.2296', '0.373', '-0.5293', '-0.2261', '0.262', '-0.2805', '0.07916', '0.2551', '0.1927', '0.2289', '0.347', '-0.4126', '-0.607', '0.06915', '-0.01573', '-0.3223', '0.024', '0.1857', '0.10834', '0.0491', '0.377', '-0.2505', '0.2218', '0.1837', '0.1613', '-0.186', '-0.01503', '-0.1973', '-0.00269', '0.442', '-0.2651', '0.4001', '0.2051', '-0.1461', '-0.0729', '-0.604', '-0.632', '-0.2917', '0.2487', '0.551', '0.4749', '0.3274', '-0.3755', '-0.9507', '0.481', '-0.2135', '-0.7505', '-0.2461', '0.4805', '0.02003', '-0.2238', '0.664', '-0.1605', '0.2979', '-1.148', '0.542', '0.2715']",,,C563721,,,,
mondo:0012272,"intellectual disability, keratoconus, febrile seizures, and sinoatrial block","['intellectual disability, keratoconus, febrile seizures, and sinoatrial block', 'mental retardation, keratoconus, febrile seizures, and sinoatrial block']",,609438,,C1836202,,,,C537452,,,,
mondo:0012273,autosomal recessive nonsyndromic hearing loss 48,"['deafness, autosomal recessive type 48', 'autosomal recessive nonsyndromic deafness 48', 'deafness, autosomal recessive 48', 'CIB2 autosomal recessive nonsyndromic deafness', 'autosomal recessive deafness 48', 'autosomal recessive nonsyndromic deafness caused by mutation in CIB2', 'DFNB48', 'autosomal recessive nonsyndromic deafness type 48']",0110505,609439,,C1836199,,,,C563720,,,,
mondo:0012274,acromesomelic dysplasia 3,"['acromesomelic dysplasia 3', 'AMDD', 'chondrodysplasia, acromesomelic, with or without genital anomalies', 'acromesomelic dysplasia, Demirhan type', 'chondrodysplasia acromesomelic with genital anomalies']",0081237,609441,,,"['-0.02695', '0.0324', '0.01881', '-0.014755', '0.03918', '-0.06146', '-0.003775', '0.04175', '-0.04636', '-0.02351', '-0.01836', '-0.006203', '-0.00915', '-0.003157', '-0.01456', '-0.007465', '0.0255', '-0.014084', '-0.010956', '-0.0703', '-0.008606', '-0.007122', '0.06964', '0.003124', '-0.0001164', '-0.01165', '-0.0123', '-0.03464', '0.002323', '-0.02664', '0.03616', '-0.00377', '0.0444', '0.01767', '0.01386', '-0.0232', '-0.02483', '-0.03265', '-0.00724', '-0.0578', '0.01124', '-0.05316', '-0.000997', '-0.003769', '-0.02823', '-0.04257', '-0.0254', '0.04272', '0.02246', '-0.003107', '0.008865', '-0.00632', '-0.002756', '-0.01061', '-0.02235', '-0.0295', '0.02573', '-0.02791', '-0.05292', '0.01642', '0.02826', '0.02072', '-0.003967', '-0.006184', '0.004704', '0.001535', '0.0353', '0.03094', '-0.0408', '0.04852', '-0.0476', '-0.001806', '0.001073', '-0.04514', '0.01347', '0.0326', '-0.01648', '-0.002647', '-0.03635', '-0.03836', '0.001819', '0.01532', '-0.02455', '0.05026', '-0.0142', '0.014366', '0.00796', '0.0453', '0.04956', '0.009575', '0.02238', '0.04446', '0.0042', '0.01915', '0.08093', '0.01707', '0.06396', '-0.0689', '-0.00515', '0.02821']",,,C537913,,,,
mondo:0012275,fetal valproate syndrome,"['valproate embryopathy, susceptibility to', 'foetal valproic acid syndrome', 'susceptibility to valproate embryopathy', 'fetal valproic acid syndrome', 'fetal valproate syndrome', 'FVS', 'valproic acid embryopathy']",0060471,609442,1906,C0236026,,C98930,,C536525,759.89,,10016524,
mondo:0012276,generalized epilepsy-paroxysmal dyskinesia syndrome,"['epilepsy, generalized, with paroxysmal dyskinesia', 'paroxysmal nonkinesigenic dyskinesia, 3, with or without generalised epilepsy', 'generalized epilepsy and paroxysmal dyskinesia', 'generalised epilepsy and paroxysmal dyskinesia', 'GEPD', 'PNKD3', 'paroxysmal nonkinesigenic dyskinesia, 3, with or without generalized epilepsy']",,609446,79137,C1836173,"['0.9253', '0.1869', '-0.2395', '-0.03035', '-0.4766', '-0.4502', '0.913', '0.3237', '-0.603', '-0.45', '-0.05624', '-0.1846', '-0.3533', '0.3154', '0.1256', '0.12213', '-0.2668', '-0.3923', '-0.596', '-0.511', '-0.1929', '0.732', '0.1263', '-0.4922', '-0.251', '-0.0724', '-0.06885', '-0.02242', '-0.3547', '0.362', '0.3262', '-0.5464', '0.183', '0.03004', '0.6577', '0.3755', '0.01642', '-0.09625', '-0.1968', '-0.49', '-0.1509', '-0.3826', '0.1874', '-0.09894', '-0.493', '-0.7544', '-0.256', '0.2206', '0.799', '0.711', '-0.2413', '0.09296', '0.04718', '-0.446', '0.0818', '-0.0893', '-0.01074', '0.1216', '-0.2443', '0.397', '-0.89', '0.578', '0.843', '-0.1837', '-0.3726', '1.487', '0.11755', '-0.01624', '-0.9785', '0.755', '0.9727', '1.023', '-0.0971', '-0.386', '0.1383', '0.7656', '0.8887', '0.6353', '-0.4192', '0.4326', '-0.2196', '0.9023', '0.5503', '0.335', '0.3237', '0.068', '0.1643', '0.776', '0.793', '0.4219', '-0.204', '-0.03412', '-0.333', '0.07367', '0.09894', '0.2443', '0.457', '-0.7227', '0.0569', '0.3105']",,,C563719,,,,
mondo:0012277,myofibrillar myopathy 4,"['late-onset distal myopathy, Markesbery-Griggs type', 'myofibrillar myopathy type 4', 'zaspopathy', 'myopathy, myofibrillar, type 4', 'MFM4', 'myopathy, myofibrillar, 4', 'LDB3 myofibrillar myopathy (disease)', 'ZASP-related myofibrillar myopathy']",0080095,609452,98912,C1836155,"['-0.769', '-0.4785', '-0.4534', '-0.2347', '0.03806', '-1.097', '0.03336', '0.898', '-1.242', '-0.02011', '-0.425', '0.253', '0.03096', '-0.1969', '0.2408', '-0.1406', '-0.23', '-0.6104', '-0.277', '-0.873', '0.4346', '-0.1011', '0.09894', '0.03079', '0.3499', '0.292', '-0.05487', '-0.1934', '-0.3904', '0.001664', '0.283', '0.1853', '-0.199', '-0.3064', '0.0144', '-0.544', '-0.0397', '-0.0915', '0.392', '-0.1296', '-0.128', '-0.2046', '0.3564', '0.8237', '-0.1094', '0.2328', '-0.7275', '0.2612', '0.05746', '0.10535', '-0.3706', '-0.02646', '-0.1644', '0.2234', '-0.3809', '-0.439', '0.917', '-0.4753', '-0.0546', '-0.07874', '0.667', '0.1329', '0.1549', '-0.3608', '-0.627', '0.518', '0.2012', '0.8335', '-0.5635', '0.239', '-0.3533', '0.04996', '0.04813', '0.2118', '0.4902', '0.12006', '-0.4985', '-0.0095', '-0.5664', '-0.292', '0.431', '-0.0689', '0.836', '0.5664', '0.11163', '0.346', '-0.4023', '0.6807', '0.259', '-0.4456', '0.4968', '0.10455', '0.2385', '-0.010155', '0.924', '-0.1427', '0.8228', '-0.4355', '-0.1954', '0.0847']",,,C563718,,,,
mondo:0012278,"supranuclear palsy, progressive, 2","['supranuclear palsy, progressive, 2', 'PSNP2']",,609454,,C1836148,,,,C563717,,,,
mondo:0012280,Goldberg-Shprintzen megacolon syndrome,"['GOSHS', 'Goldberg-Shprintzen syndrome', 'Goldberg-Shprintzen megacolon syndrome', 'megacolon-microcephaly syndrome']",0060481,609460,66629,C1836123,"['-0.106', '-0.01558', '0.11896', '-0.4946', '0.6816', '-0.3372', '0.1249', '0.867', '-0.91', '-0.9897', '0.1552', '-0.608', '0.01106', '-0.1849', '-0.1718', '0.05753', '-0.4907', '-0.7354', '-0.3713', '-0.4912', '-0.02017', '0.006447', '-0.05664', '0.03494', '0.5063', '-0.27', '-0.2399', '0.672', '0.555', '-0.1098', '0.356', '-0.442', '0.2144', '0.06213', '-0.08655', '0.1313', '-0.563', '-0.4954', '-0.4065', '-0.0694', '-0.4053', '-0.2622', '0.2043', '-0.0362', '0.478', '-0.2515', '0.4292', '0.62', '-0.4382', '-0.275', '-0.3323', '0.5366', '-0.3872', '-0.02788', '-0.3657', '-0.07245', '-0.543', '0.1896', '-0.3298', '0.08716', '0.3372', '0.2251', '0.07227', '0.2155', '0.01619', '0.10706', '0.812', '0.4482', '-0.9785', '-0.05643', '-0.0577', '-0.2637', '-0.0915', '0.406', '-0.6377', '-0.1439', '0.383', '-0.555', '-0.2627', '0.2876', '0.214', '0.1664', '-0.05264', '0.6714', '0.1321', '0.3652', '-0.3901', '0.06366', '-0.09314', '0.737', '-0.06964', '0.4067', '-0.1214', '0.1499', '0.5522', '-0.1353', '0.298', '-0.145', '0.3472', '0.2903']",,,C537279,,,,
mondo:0012282,Al-Gazali syndrome,"['eye defects arachnodactyly cardiopathy', 'Al Gazali syndrome', 'Al-Gazali syndrome', 'Al Gazali Al Talabani syndrome']",,609465,2725,C1836121,,,,C536817,,,,
mondo:0012283,"cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss","['cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss']",,609466,,C1836120,,,,C536427,,,,
mondo:0012284,"nephropathy, progressive, with deafness","['Alport/focal segmental glomerulosclerosis-like syndrome', 'nephropathy, progressive, with deafness', 'Nede']",,609469,,C1836119,,,,C563713,,,,
mondo:0012285,left ventricular noncompaction 2,"['left ventricular noncompaction 2', 'LVNC2']",,609470,,C1836118,,,,,,,,
mondo:0012286,"myopathy, autophagic vacuolar, infantile-onset","['myopathy, autophagic vacuolar, infantile-onset']",,609500,,,,,,,,,,
mondo:0012287,"Stickler syndrome, type I, nonsyndromic ocular","['Stickler syndrome, atypical', 'Stickler syndrome, type i, nonsyndromic ocular', 'rhegmatogenous retinal detachment, autosomal dominant', 'Stickler syndrome, type I, predominantly ocular']",,609508,,C1836080,"['-0.00488', '0.02069', '0.00995', '-0.00814', '0.002092', '-0.01875', '-0.002201', '0.03052', '-0.03035', '-0.01945', '-0.00818', '-0.00726', '0.00941', '0.01458', '-0.004154', '-0.01776', '0.0097', '-0.01768', '-0.01344', '-0.04395', '0.000262', '-0.01714', '0.02963', '-0.006454', '0.01441', '-0.003624', '-0.00519', '-0.00844', '0.01598', '-0.01076', '0.01985', '0.00199', '0.02557', '0.001841', '0.01165', '-0.01461', '-0.007637', '-0.01898', '0.00423', '-0.0309', '0.005943', '-0.0239', '0.00936', '-0.000909', '-0.00937', '-0.02856', '-0.004784', '0.02026', '0.013115', '0.0135', '-0.004185', '-0.002623', '0.006454', '-0.01576', '-0.0193', '-0.0191', '0.015175', '-0.01628', '-0.02573', '0.012726', '0.0179', '0.005974', '-0.001223', '0.005127', '0.00628', '0.003956', '0.02313', '0.0213', '-0.0334', '0.01968', '-0.02582', '0.002844', '-0.003294', '-0.0167', '0.008316', '0.01636', '0.01098', '-0.00985', '-0.012825', '-0.00991', '-0.006073', '-0.01047', '-0.0117', '0.02846', '-0.009865', '-0.004555', '-0.0003173', '0.03845', '0.02927', '0.01202', '0.006626', '0.02959', '-0.003601', '0.004448', '0.0418', '0.01378', '0.01785', '-0.02858', '0.001045', '-9.096e-05']",,,C563709,,,,
mondo:0012288,iridogoniodysgenesis and skeletal anomalies,['iridogoniodysgenesis and skeletal anomalies'],,609515,,C1836074,,,,C535534,,,,
mondo:0012289,myofibrillar myopathy 5,"['MFM5', 'myofibrillar myopathy type 5', 'myopathy, myofibrillar, 5', 'myopathy, myofibrillar, type 5', 'myopathy, myofibrillar, filamin C-related', 'filaminopathy, autosomal dominant', 'FLNC myofibrillar myopathy (disease)', 'filaminopathy', 'muscle filaminopathy']",0080096,609524,171445,,"['-0.5103', '-0.153', '0.1635', '-0.2009', '-0.2715', '-0.513', '0.2651', '0.721', '-0.6055', '0.0608', '-0.1215', '0.001608', '-0.02203', '0.1829', '-0.0627', '-0.04178', '-0.3738', '-0.0709', '-0.1015', '-0.538', '0.1515', '0.1647', '0.2478', '0.1304', '0.02151', '-0.1536', '0.3025', '-0.133', '-0.3828', '0.1548', '0.0975', '-0.03937', '0.074', '-0.10516', '0.00903', '-0.4485', '0.03114', '-0.000609', '0.2874', '-0.01484', '0.06464', '-0.3616', '-0.1868', '0.4749', '-0.06256', '0.2896', '-0.4932', '0.4912', '-0.1218', '0.1757', '-0.2717', '0.2057', '-0.04196', '0.1387', '-0.0671', '-0.4058', '0.2256', '-0.171', '-0.04678', '-0.1782', '0.204', '0.208', '-0.2428', '-0.1158', '-0.3496', '-0.1415', '0.286', '0.814', '-0.1547', '0.0632', '-0.1548', '0.2466', '0.2471', '0.09143', '0.242', '0.2502', '-0.0883', '-0.1573', '-0.01505', '-0.1687', '0.2377', '-0.2368', '0.4583', '0.4238', '0.07574', '0.3267', '-0.10333', '0.215', '0.2932', '-0.3608', '0.2347', '-0.06094', '0.0803', '0.3496', '0.738', '0.1633', '0.5786', '-0.2319', '-0.286', '0.08997']",,,C537932,,,,
mondo:0012290,CEDNIK syndrome,"['CEDNIK syndrome', 'cerebral dysgenesis, neuropathy, ichthyosis and keratoderma syndrome', 'cerebral dysgenesis, neuropathy, ichthyosis, and palmoplantar keratoderma syndrome', 'cerebral dysgenesis-neuropathy-ichthyosis-palmoplantar keratoderma syndrome']",0060337,609528,66631,C1836033,"['-0.2754', '0.5957', '0.1041', '-0.02333', '0.01253', '-0.5015', '-0.6147', '-0.1902', '-0.2893', '-0.2085', '-0.342', '-0.4033', '-0.32', '-0.2986', '-0.04816', '0.266', '0.0342', '-0.502', '-0.4285', '-0.638', '0.3022', '0.1498', '0.7056', '-0.4038', '0.1927', '0.2445', '0.301', '0.2998', '0.0348', '-0.539', '0.3557', '0.069', '0.4685', '0.0012245', '-0.013176', '0.2295', '-0.2084', '0.02612', '-0.4082', '0.04138', '0.2166', '-0.3848', '0.1548', '-0.2', '-0.1159', '-0.2861', '0.09955', '-0.2151', '0.01525', '-0.659', '-0.05737', '-0.1054', '-0.3381', '0.0905', '-0.2375', '-0.439', '0.4316', '0.3992', '-0.34', '0.1399', '0.1791', '-0.3723', '0.1692', '0.2976', '-0.0866', '0.10486', '0.2532', '0.537', '-0.6577', '0.3972', '-0.653', '0.184', '-0.0318', '0.4646', '-0.02585', '0.2566', '0.1418', '0.528', '0.101', '-0.2228', '0.302', '0.3606', '-0.01865', '0.512', '0.05377', '-0.2454', '-0.02048', '0.3271', '-0.3127', '0.0681', '0.4001', '0.3677', '0.2585', '-0.1109', '0.6733', '0.2494', '0.2954', '-0.6743', '0.2257', '0.0698']",,,C537943,,,,
mondo:0012291,immunoglobulin A deficiency 2,"['immunoglobulin a deficiency 2', 'selective IgA deficiency disease caused by mutation in TNFRSF13B', 'IGAD2', 'IgA, selective deficiency of, TACI-related', 'Immunoglobulin A, selective deficiency of, TACI related', 'Immunoglobulin a deficiency type 2', 'TNFRSF13B selective IgA deficiency disease', 'Immunoglobulin A, selective deficiency of, TACI-related', 'IMMUNOGLOBULIN A deficiency 2', 'IgA, selective deficiency of, TACI related']",,609529,,C1836032,,,,C536291,,,,
mondo:0012292,"hepatitis C virus, susceptibility to","['Hepatitis C Virus infection, response to therapy of', 'Hepatitis C Virus, resistance to', 'hepatitis C virus, response to therapy of', 'HCV, resistance to', 'HCV, susceptibility to', 'hepatitis C virus, susceptibility to']",,609532,,C2750389,,,,,,,,
mondo:0012293,autosomal recessive nonsyndromic hearing loss 23,"['autosomal recessive nonsyndromic deafness caused by mutation in PCDH15', 'deafness, autosomal recessive 23', 'autosomal recessive nonsyndromic deafness type 23', 'autosomal recessive nonsyndromic deafness 23', 'DFNB23', 'PCDH15 autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive type 23', 'autosomal recessive deafness 23']",0110481,609533,,C1836027,,,,C563705,,,,
mondo:0012295,complement component 5 deficiency,"['complement deficiency caused by mutation in C5', 'C5D', 'complement component 5 deficiency', 'C5 deficiency', 'C5 complement deficiency', 'dysfunction of the fifth component of complement (C5)']",8158,609536,,C0343047,,C9469,,,,,,
mondo:0012296,lipomyelomeningocele,"['lipomyelomeningocele', 'familial lipomyelomeningocele']",,609537,268835,C1836022,,,,C537030,214.8,,,
mondo:0012297,SPOAN syndrome,"['spastic paraplegia-optic atrophy-neuropathy syndrome', 'spastic paraplegia, optic atropy, and neuropathy syndrome', 'SPOAN', 'spastic paraplegia, optic atrophy, and neuropathy', 'spastic paraplegia, optic atropy, and neuropathy']",0060491,609541,320406,C1836010,"['-0.4143', '0.1768', '0.06903', '-0.1781', '-0.03378', '-0.946', '-0.1675', '0.146', '-0.5835', '-0.4001', '0.1687', '0.2473', '-0.1776', '-0.0922', '0.4624', '-0.00383', '-0.0953', '-0.3071', '0.2208', '-0.1813', '0.1968', '-0.4666', '0.3252', '0.1954', '-0.05283', '0.3223', '0.1088', '-0.00921', '-0.1483', '-0.1394', '0.3933', '0.05106', '0.4226', '0.557', '-0.00972', '-0.702', '-0.0672', '-0.4417', '-0.4956', '-0.471', '0.2764', '-0.7427', '-0.02179', '0.7485', '-0.4888', '-0.2207', '-0.3765', '0.3975', '0.3323', '0.2832', '-0.2556', '-0.0915', '-0.06757', '-0.3696', '0.5005', '-0.673', '1.008', '0.0894', '-0.2487', '0.519', '-0.0206', '0.02351', '0.363', '0.4817', '-0.4773', '-0.0802', '0.2429', '0.9365', '-0.007053', '0.5244', '-0.5063', '-0.1467', '0.3235', '-0.2157', '0.7354', '0.2576', '-0.2427', '0.3853', '-0.2893', '0.044', '0.212', '-0.04922', '0.2783', '1.072', '-0.326', '-0.0443', '0.1122', '0.3782', '0.1602', '0.07214', '0.4172', '0.2156', '0.1732', '0.03497', '0.517', '0.2136', '0.8145', '-0.1024', '-0.007935', '-0.0378']",,,C563702,,,,
mondo:0012298,"omphalocele, diaphragmatic hernia, and radial ray defects","['omphalocele, diaphragmatic hernia, and radial ray defects', 'Gershoni-Baruch syndrome']",,609545,,C1836007,,,,C563701,,,,
mondo:0012299,nanophthalmos 2,"['nanophthalmos 2', 'MFRP nanophthalmia', 'nanophthalmos, autosomal recessive', 'nanophthalmos type 2', 'nanophthalmia caused by mutation in MFRP', 'NNO2', 'Nanophthalmia 2']",,609549,,C1836006,,,,C563700,,,,
mondo:0012300,"prostate cancer, hereditary, 6","['HPC6', 'prostate cancer, hereditary, 6', 'prostate cancer, susceptibility to', 'prostate cancer, hereditary, type 6']",,609558,,C1836005,,,,C563699,,,,
mondo:0012301,"mitochondrial DNA depletion syndrome, myopathic form","['mitochondrial DNA depletion myopathy, Tk2-related', 'mtDNA depletion syndrome, myopathic form', 'mitochondrial DNA depletion syndrome type 2', 'mitochondrial DNA depletion syndrome 2 (myopathic type)', 'MTDPS2', 'mitochondrial DNA depletion syndrome 2']",0080120,609560,254875,C3501891,"['-0.3843', '0.1973', '0.2815', '0.1228', '0.08276', '-0.752', '0.1171', '0.4202', '-0.6025', '-0.138', '-0.015305', '-0.2695', '0.1024', '-0.02798', '-0.11957', '-0.04645', '-0.4575', '-0.2795', '-0.0655', '-0.789', '0.05624', '-0.1768', '0.5103', '0.1991', '0.3323', '0.1241', '-0.2134', '-0.09247', '-0.1335', '0.01511', '-0.1534', '0.1628', '0.5', '0.1763', '-0.04617', '-0.1957', '-0.4312', '0.1753', '-0.3486', '-0.0846', '0.2335', '-0.6475', '-0.3403', '-0.03268', '0.1616', '-0.0133', '-0.3403', '0.1293', '0.271', '0.1664', '-0.3345', '-0.08136', '-0.02878', '0.009575', '-0.2382', '-0.9863', '-0.001734', '0.01846', '0.02406', '0.3733', '0.1967', '-0.4792', '0.2246', '0.1043', '-0.432', '-0.2603', '0.3313', '0.2361', '-0.377', '0.297', '-0.2312', '0.07904', '0.44', '0.3513', '0.02971', '0.4578', '0.01788', '-0.1447', '-0.2295', '0.03177', '0.557', '0.085', '-0.4731', '0.0747', '-0.1029', '0.2627', '0.2437', '0.1823', '0.4016', '-0.1637', '0.4917', '0.1538', '0.2227', '-0.0618', '0.2373', '0.5586', '0.2769', '-0.4402', '0.1399', '-0.07446']",,,C563698,359.89,,,
mondo:0012302,parietal foramina 3,"['parietal foramina 3', 'PFM3']",,609566,,C1835980,,,,C563697,,,,
mondo:0012303,"migraine with or without aura, susceptibility to, 8","['Mgr8', 'migraine with or without aura, susceptibility to, type 8', 'migraine with or without aura, susceptibility to, 8', 'migraine, susceptibility to, 8']",,609570,,,,,,,,,,
mondo:0012304,photoparoxysmal response 2,"['PPR2', 'photoparoxysmal response with or without idiopathic generalized epilepsy', 'photoparoxysmal response 2', 'photoparoxysmal response with or without idiopathic generalised epilepsy']",,609572,,C1835967,,,,,,,,
mondo:0012305,photoparoxysmal response 3,"['PPR3', 'photoparoxysmal response 3', 'photoparoxysmal response with or without myoclonic epilepsy']",,609573,,C1835966,,,,C563695,,,,
mondo:0012306,"cardiomyopathy, familial restrictive, 2","['RCM2', 'cardiomyopathy, familial restrictive, 2']",0111426,609578,,C1865071,,,,C566512,,,,
mondo:0012307,"familial scaphocephaly syndrome, McGillivray type","['scaphocephaly, maxillary retrusion, and mental retardation', 'scaphocephaly, maxillary retrusion, and intellectual disability', 'scaphocephaly-macrocephaly-maxillary retrusion-intellectual disability syndrome']",,609579,168624,C1865070,"['-0.07684', '0.1322', '0.02524', '-0.3564', '0.02339', '-0.4705', '-0.1631', '0.6353', '-0.333', '-0.1671', '0.04742', '-0.1178', '0.1289', '-0.4753', '-0.2026', '-0.2493', '0.515', '-0.1859', '0.1192', '-0.3772', '0.0879', '0.2522', '0.43', '-0.484', '0.423', '0.1553', '-0.1726', '-0.4585', '0.584', '-0.5703', '0.2722', '0.0476', '0.5293', '0.1478', '0.1567', '-0.3745', '-0.4333', '-0.704', '-0.2832', '-0.501', '0.4104', '-0.3174', '0.05112', '-0.4702', '0.02538', '-0.00899', '-0.07886', '0.1288', '-0.1752', '-0.35', '0.0757', '-0.1814', '-3.004e-05', '0.0947', '-0.51', '-0.3455', '-0.365', '-0.3298', '0.10364', '0.3982', '-0.01326', '-0.1543', '0.1984', '-0.05878', '-0.10986', '0.1342', '-0.02258', '0.4128', '-0.917', '0.3306', '0.0327', '0.369', '0.0823', '0.05325', '-0.4219', '0.3953', '0.04675', '-0.02544', '-0.3997', '0.00626', '-0.00771', '0.4905', '-0.4568', '0.6006', '0.2937', '0.269', '-0.296', '0.1355', '0.3599', '0.1361', '-0.196', '0.6494', '0.3987', '0.162', '1.008', '0.04773', '0.2727', '-0.536', '0.4011', '0.09393']",,,C566511,,,,
mondo:0012308,Joubert syndrome with renal defect,"['Joubert syndrome 4', 'JS-R', 'Joubert syndrome type 4', 'JBTS4', 'Joubert syndrome with renal anomalies']",0110999,609583,220497,,,C74997,,C536296,,,,
mondo:0012309,parietal foramina 2,"['parietal foramina 2', 'PFM2', 'ALX4 parietal foramina', 'parietal foramina type 2', 'parietal foramina caused by mutation in ALX4']",,609597,,C1865044,,,,C566510,,,,
mondo:0012310,"fibrosis of extraocular muscles, congenital, with synergistic divergence","['external ophthalmoplegia, synergistic divergence, jaw winking, and oculocutaneous hypopigmentation', 'fibrosis of extraocular muscles, congenital, with synergistic divergence', 'external ophthalmoplegia with synergistic divergence', 'congenital fibrosis syndrome with synergistic divergence']",,609612,,C1865040,,,,C566508,,,,
mondo:0012311,"spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness","['spondylomegaepiphyseal dysplasia with upper limb mesomelia, punctate calcifications, and deafness']",,609616,,C1865022,,,,C566507,,,,
mondo:0012312,short QT syndrome type 1,"['short QT syndrome type 1', 'SQTS', 'KCNH2 short QT syndrome', 'SQT1', 'short QT syndrome caused by mutation in KCNH2', 'short QT syndrome 1']",,609620,,C1865020,,,,C566506,,,,
mondo:0012313,short QT syndrome type 2,"['SQT2', 'short QT syndrome 2', 'short QT syndrome type 2', 'short QT syndrome caused by mutation in KCNQ1', 'KCNQ1 short QT syndrome']",,609621,,C1865019,,,,C566505,,,,
mondo:0012314,short QT syndrome type 3,"['SQT3', 'short QT syndrome 3', 'KCNJ2 short QT syndrome', 'short QT syndrome type 3', 'short QT syndrome caused by mutation in KCNJ2']",,609622,,C1865018,,,,C566504,,,,
mondo:0012315,distal 10q deletion syndrome,"['distal deletion 10q', 'telomeric deletion 10q', 'distal monosomy 10q', 'distal monosomy type 10q', '10q monosomy', 'chromosome 10q deletion', 'terminal chromosome 10Q26 deletion syndrome', '10q deletion', 'chromosome 10q26 deletion syndrome', 'partial monosomy 10q', 'terminal chromosome 10q26 deletion syndrome', 'deletion 10q', 'monosomy 10qter', 'monosomy 10q']",0060390,609625,96148,C4305277,,,,C567182,,,,
mondo:0012316,Majeed syndrome,"['MAJEED syndrome', 'CDA and CRMO', 'chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic Anemia, and neutrophilic dermatosis', 'MJDS', 'chronic recurrent multifocal osteomyelitis-congenital dyserythropoietic anemia-neutrophilic dermatosis syndrome', 'chronic recurrent multifocal osteomyelitis, congenital', 'congenital dyserythropoietic anaemia and chronic recurrent multifocal osteomyelitis', 'congenital dyserythropoietic anemia and chronic recurrent multifocal osteomyelitis', 'dyserythropoietic anemia, and neutrophilic dermatosis', 'Majeed syndrome']",,609628,77297,C1864997,"['-0.0939', '0.297', '-0.7607', '-0.4448', '0.6396', '-0.3894', '-0.04443', '0.907', '-0.1483', '0.06018', '0.01111', '0.062', '0.548', '0.518', '-0.3508', '-0.6055', '0.10065', '-0.0329', '-0.397', '-1.31', '0.2078', '0.1387', '0.1613', '-0.8623', '0.3484', '0.1571', '0.2856', '-0.1615', '-0.3496', '-0.7383', '0.1484', '-0.6016', '-0.1996', '0.7866', '-0.2078', '-0.573', '-0.3906', '-0.7305', '-0.5957', '0.4968', '-0.3867', '-0.3481', '0.0878', '-0.04797', '0.1671', '-0.151', '-0.3687', '-0.4604', '-0.11896', '-0.284', '-0.2727', '0.3743', '0.2395', '0.6357', '0.2874', '-0.3315', '-0.3594', '0.3057', '-0.03088', '0.3171', '0.2451', '0.666', '-0.327', '-0.942', '0.2715', '-0.4624', '0.1068', '0.4524', '0.0466', '0.76', '0.0706', '-0.551', '0.716', '0.0891', '0.3108', '0.1098', '-0.2086', '0.2393', '0.0367', '-0.2433', '0.3892', '0.1583', '-0.12286', '0.3381', '-0.1857', '0.5103', '0.4197', '1.255', '-0.283', '0.7686', '0.2805', '0.004738', '-0.3179', '-0.09283', '0.313', '0.6377', '0.1993', '-0.798', '-0.2507', '-0.1814']",C119058,,C537839,759.89,,10072223,
mondo:0012317,"visceral neuropathy, familial, 3, autosomal dominant","['pseudoobstruction, chronic intestinal, neuropathic', 'visceral neuropathy, familial, autosomal dominant', 'pseudoobstruction, idiopathic intestinal', 'enteric neuropathy, familial']",0080682,609629,,C1864996,,,,,,,,
mondo:0012318,"leukemia, chronic lymphocytic, susceptibility to, 1","['leukemia, chronic lymphocytic, susceptibility to, 1', 'leukemia, chronic lymphocytic, susceptibility to, type 1', 'Clls1']",,609630,,,,,,,,,,
mondo:0012319,major affective disorder 3,"['major affective disorder 3, early onset', 'bipolar affective disorder, early-onset', 'major affective disorder 3', 'MAFD3', 'MAJOR affective disorder 3']",,609633,,C1864994,,,,C566501,,,,
mondo:0012320,"migraine, familial hemiplegic, 3","['migraine, familial hemiplegic, type 3', 'familial or sporadic hemiplegic migraine caused by mutation in SCN1A', 'FHM3', 'SCN1A familial or sporadic hemiplegic migraine', 'migraine, familial hemiplegic, 3']",0111183,609634,,C1864987,,,,C566500,,,,
mondo:0012321,Alzheimer disease 10,"['Alzheimer disease 10', 'Alzheimer disease, familial, 10', 'Alzheimer disease familial 10', 'Ad10', 'Alzheimer disease-10', 'Alzheimer^s disease type 10', 'Alzheimer disease type 10', 'Alzheimer^s disease 10', 'AD10']",0110043,609636,,C1864828,,,,C566465,,,,
mondo:0012322,holoprosencephaly 5,"['holoprosencephaly 5', 'HPE5', 'holoprosencephaly type 5', 'holoprosencephaly caused by mutation in ZIC2', 'ZIC2 holoprosencephaly']",0110878,609637,,C1864827,,C75460,,C566464,,,,
mondo:0012323,lethal acantholytic epidermolysis bullosa,"['epidermolysis bullosa, lethal acantholytic', 'EBLA', 'lethal acantholytic epidermolysis bullosa', 'LAEB']",,609638,158687,C1864826,"['0.784', '-0.1582', '-0.5186', '0.0715', '-0.0733', '-0.7017', '-0.501', '0.575', '-0.03476', '-0.5605', '0.2898', '-0.5483', '-0.9253', '0.4033', '-0.6724', '0.3176', '0.1636', '-1.25', '-0.487', '-0.9346', '-0.3684', '-0.06', '0.4712', '0.574', '0.1426', '0.2399', '-1.108', '0.77', '-0.2803', '-0.895', '0.1582', '-0.07764', '-0.4065', '-0.2001', '0.0919', '-0.0637', '-1.121', '0.2266', '1.193', '-0.6753', '0.1908', '-0.4668', '0.1516', '-0.05655', '0.008446', '-0.243', '-0.39', '0.1368', '0.4302', '-0.1936', '-0.6426', '-0.7056', '0.577', '-0.1837', '-0.1873', '-0.591', '-0.2612', '1.141', '-0.861', '-0.3188', '0.06604', '0.4382', '0.1279', '0.4688', '0.863', '0.708', '0.2207', '0.2052', '-0.6724', '0.1349', '-0.06177', '-0.052', '-0.532', '-0.1362', '-0.03044', '0.1232', '-0.09546', '0.2241', '0.0651', '-0.02812', '-1.16', '0.2168', '-0.313', '-0.2185', '0.3066', '0.2568', '-1.021', '0.7812', '1.026', '0.2238', '-0.4243', '0.3406', '-0.1531', '0.6724', '0.0652', '1.027', '0.341', '-0.5063', '0.713', '0.08606']",,,C535493,,,,
mondo:0012324,Frias syndrome,"['monosomy 14q22q23', 'Growth deficiency, Facial anomalies, and brachydactyly', '14q22q23 microdeletion syndrome', 'Frias syndrome', 'chromosome 14Q22 deletion syndrome', '14q22-q23 microdeletion syndrome', 'Del(14)(q22q23)', 'monosomy 14q22-q23']",,609640,264200,C1864825,,,,C535639,,,,
mondo:0012325,Nguyen syndrome,"['MCA/Mr with hypocholesterolemia due to familial hypobetalipoproteinemia', 'MCA/MR syndrome with hypocholesterolemia due to familial hypobetalipoproteinemia', 'Nguyen syndrome']",,609643,,C1864823,,,,C536115,,,,
mondo:0012326,autosomal recessive nonsyndromic hearing loss 42,"['deafness, autosomal recessive type 42', 'autosomal recessive nonsyndromic deafness caused by mutation in ILDR1', 'DFNB42', 'autosomal recessive deafness 42', 'deafness, autosomal recessive 42', 'autosomal recessive nonsyndromic deafness 42', 'autosomal recessive nonsyndromic deafness type 42', 'ILDR1 autosomal recessive nonsyndromic deafness']",0110500,609646,,C1864818,,,,C566460,,,,
mondo:0012327,autosomal recessive nonsyndromic hearing loss 46,"['autosomal recessive deafness 46', 'DFNB46', 'autosomal recessive nonsyndromic deafness type 46', 'autosomal recessive nonsyndromic deafness 46', 'deafness, autosomal recessive 46']",0110503,609647,,C1864815,,,,C566459,,,,
mondo:0012328,trichilemmal cyst,"['TRICY1', 'Tricholemmal cyst', 'Pilar cyst', 'trichilemmal cyst 1']",,609649,,C2266788,,,,,,,,
mondo:0012329,short stature and Facioauriculothoracic malformations,['short stature and Facioauriculothoracic malformations'],,609654,,C1864791,,,,C566457,,,,
mondo:0012330,talo-patello-scaphoid osteolysis,"['talo-patello-scaphoid osteolysis, synovitis, and short fourth metacarpals', 'singh-Williams-McAlister syndrome']",,609655,50809,C1864784,,,,C536894,,,,
mondo:0012331,"migraine with aura, susceptibility to, 9","['Mgr9', 'migraine with aura, susceptibility to, type 9', 'migraine with aura, susceptibility to, 9']",,609670,,,,,,,,,,
mondo:0012333,autosomal recessive nonsyndromic hearing loss 53,"['deafness, autosomal recessive 53', 'autosomal recessive deafness 53', 'deafness, autosomal recessive type 53', 'COL11A2 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness 53', 'autosomal recessive nonsyndromic deafness type 53', 'autosomal recessive nonsyndromic deafness caused by mutation in COL11A2', 'DFNB53']",0110509,609706,,C1864746,,,,C566453,,,,
mondo:0012334,hereditary spastic paraplegia 29,"['SPG29', 'spastic paraplegia 29', 'hereditary spastic paraplegia type 29', 'autosomal dominant spastic paraplegia 29', 'autosomal dominant spastic paraplegia type 29', 'spastic paraplegia 29, autosomal dominant']",0110780,609727,101009,C1857855,,,,C536863,,,,
mondo:0012335,obesity due to pro-opiomelanocortin deficiency,"['obesity, adrenal insufficiency, and red hair due to POMC deficiency', 'PROOPIOMELANOCORTIN deficiency', 'obesity, early-onset, with adrenal insufficiency and Red hair', 'obesity, early-onset, with adrenal insufficiency and RED hair', 'obesity, early-onset, adrenal insufficiency, and Red hair', 'POMC deficiency', 'OBAIRH']",,609734,71526,C1857854,"['-0.323', '0.4927', '-0.395', '0.931', '-0.3235', '-0.874', '0.2122', '0.5854', '-0.2487', '-0.664', '-0.1935', '0.4055', '0.02429', '0.1135', '-0.789', '-0.63', '-0.2201', '0.976', '-0.766', '-0.825', '-0.002144', '-0.5273', '0.3474', '-0.3608', '0.223', '0.1505', '-0.2957', '-0.424', '0.0681', '-0.1266', '0.433', '-0.385', '0.4744', '0.1254', '-0.303', '-0.4077', '-0.7334', '0.1809', '0.3154', '0.10565', '0.0894', '-0.1567', '-0.764', '0.308', '0.03952', '-0.5503', '0.3635', '0.1371', '0.2368', '0.00724', '-0.5435', '0.0915', '0.6304', '-0.2502', '-0.286', '0.871', '-0.06976', '-0.2052', '-0.1077', '-0.4255', '0.4612', '0.2646', '-0.3445', '-0.518', '-0.0808', '0.7607', '-0.4216', '0.3748', '0.3955', '0.3962', '0.3547', '0.2195', '-0.0945', '-0.2808', '0.4512', '-0.6743', '-0.2578', '-0.1741', '-1.215', '0.5356', '0.08606', '0.886', '0.10144', '-0.0726', '0.9717', '0.5337', '0.2756', '0.1213', '0.813', '0.2708', '-0.09766', '0.2498', '-0.281', '0.6885', '0.58', '0.204', '0.00938', '-0.1455', '-0.1688', '-0.2917']",,,C565726,255.5,,,
mondo:0012336,cataract 22 multiple types,"['CTRCT22', 'cataract 22', 'CRYBB3 early-onset non-syndromic cataract', 'cataract 22, multiple types', 'autosomal recessive congenital nuclear cataract 2', 'cataract, congenital nuclear, autosomal recessive 2', 'CATCN2', 'early-onset non-syndromic cataract caused by mutation in CRYBB3']",0110268,609741,98991,C1857853,,,,C565725,,,,
mondo:0012338,"epilepsy, idiopathic generalized, susceptibility to, 4","['epilepsy, idiopathic generalized, susceptibility to, 4', 'epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 10', 'EIG4', 'epilepsy, idiopathic generalized, susceptibility to 4']",0111319,609750,,,,,,,,,,
mondo:0012339,"celiac disease, susceptibility to, 4","['celiac disease caused by mutation in MYO9B', 'celiac disease, susceptibility to, type 4', 'celiac disease, susceptibility to, 4', 'coeliac disease caused by mutation in MYO9B', 'CELIAC4', 'gluten-sensitive enteropathy, susceptibility to, 4', 'susceptibility to coeliac disease 4', 'susceptibility to celiac disease 4', 'MYO9B celiac disease', 'MYO9B coeliac disease', 'coeliac disease, susceptibility to, type 4']",,609753,,,,,,,,,,
mondo:0012340,"celiac disease, susceptibility to, 2","['celiac disease, susceptibility to, 2', 'CELIAC2', 'gluten-sensitive enteropathy, susceptibility to, 2']",,609754,,,,,,,,,,
mondo:0012341,"celiac disease, susceptibility to, 3","['susceptibility to coeliac disease 3', 'celiac disease, susceptibility to, type 3', 'CTLA4 coeliac disease', 'coeliac disease, susceptibility to, type 3', 'celiac disease, susceptibility to, 3', 'CTLA4 celiac disease', 'celiac disease caused by mutation in CTLA4', 'gluten-sensitive enteropathy, susceptibility to, 3', 'susceptibility to celiac disease 3', 'coeliac disease caused by mutation in CTLA4', 'CELIAC3']",,609755,,,,,,,,,,
mondo:0012342,7q11.23 microduplication syndrome,"['Wbs triplication syndrome', 'Somerville-Van Der Aa syndrome', 'chromosome 7Q11.23 Duplication syndrome', 'trisomy 7q11.23', 'dup(7)(q11.23)', 'Williams-Beuren region DUPLICATION syndrome', 'chromosome 7Q11.23 triplication syndrome', 'Wbs Duplication syndrome', '7q11.23 duplication syndrome']",0080926,609757,96121,C4512054,,,,C565723,,,,
mondo:0012343,"aortic aneurysm, familial abdominal, 2","['aortic aneurysm, familial abdominal, 2', 'aortic aneurysm, familial abdominal 2', 'AAA2']",,609782,,C1853364,,,,C565229,,,,
mondo:0012344,Alzheimer disease 11,"['Alzheimer^s disease 11', 'AD11', 'Alzheimer disease-11', 'Alzheimer^s disease type 11', 'Alzheimer disease 11', 'Alzheimer disease, familial, 11', 'Ad11', 'Alzheimer disease type 11']",0110044,609790,,C1853360,,,,C565228,,,,
mondo:0012345,acral peeling skin syndrome,"['acral peeling skin syndrome', 'peeling skin syndrome 2', 'localised PSS', 'localized PSS', 'acral deciduous skin', 'localized deciduous skin', 'peeling skin syndrome, acral type', 'PSS2', 'peeling skin syndrome type 2', 'acral PSS', 'localised deciduous skin']",,609796,263534,C1853354,"['0.1521', '-0.1521', '-0.399', '-0.212', '0.3403', '-0.432', '-0.1626', '-0.2283', '-0.01593', '-0.3174', '-0.146', '0.2979', '-0.1741', '0.08954', '0.0227', '0.71', '0.4019', '-0.3005', '0.0823', '-0.8438', '-0.87', '-0.3225', '0.462', '-0.3096', '-0.2145', '-0.04395', '-0.609', '0.2874', '-0.2241', '-0.4934', '-0.1676', '-0.2683', '-0.366', '0.3313', '0.2081', '-0.0998', '-0.1561', '-0.3042', '0.3425', '0.0492', '-0.02505', '-0.482', '0.2913', '-0.2654', '0.2598', '-0.2352', '-0.527', '0.2489', '0.06586', '-0.002249', '-0.2686', '-0.448', '0.707', '0.3901', '-0.5137', '0.1826', '0.3826', '-0.03104', '-0.6396', '-0.318', '0.2117', '0.587', '-0.3867', '0.003887', '-0.1292', '0.4675', '0.3142', '0.645', '0.06934', '0.6035', '-0.2231', '-0.596', '0.0653', '0.1971', '0.5083', '-0.03345', '-0.2107', '0.0405', '0.1375', '-0.11316', '0.05774', '-0.3433', '0.3223', '-0.05286', '-0.0765', '0.131', '-0.187', '0.5405', '0.4412', '-0.2588', '0.5664', '0.4497', '-0.1205', '0.567', '0.21', '0.2302', '0.5312', '-0.8027', '-0.1677', '0.3325']",,,C536316,,,,
mondo:0012346,"generalized epilepsy with febrile seizures plus, type 4","['Gefs+, type 4', 'generalized epilepsy with febrile seizures plus, type 4', 'GEFSP4']",0111293,609800,,C1853345,,,,C565227,,,,
mondo:0012347,"hamartoma, Precalcaneal congenital fibrolipomatous","['Pcfh', 'hamartoma, Precalcaneal congenital fibrolipomatous']",,609808,,C1853298,,,,C565226,,,,
mondo:0012348,maturity-onset diabetes of the young type 8,"['maturity-onset diabetes of the young, type 8', 'maturity-onset diabetes of the young type 8 with exocrine dysfunction', 'CEL maturity-onset diabetes of the young (disease)', 'diabetes-pancreatic exocrine dysfunction syndrome', 'diabetes mellitus MODY type 8', 'MODY8', 'MODY type 8', 'maturity-onset diabetes of the young, type 8, with exocrine dysfunction', 'diabetes and pancreatic exocrine', 'type 8 maturity-onset diabetes of the young', 'maturity-onset diabetes of the young, type VIII', 'DPED', 'diabetes and pancreatic exocrine dysfunction']",0111105,609812,,,,,,C565225,,,,
mondo:0012349,"spondylocostal dysostosis 3, autosomal recessive","['spondylocostal dysostosis 3, autosomal recessive', 'spondylocostal dysostosis 3', 'SCOD3', 'LFNG autosomal recessive spondylocostal dysostosis', 'SCDO3']",0112361,609813,,C1853296,,,,,,,,
mondo:0012350,complement factor H deficiency,"['CFHD', 'Cfh deficiency', 'complement factor H deficiency', 'factor H deficiency']",,609814,93571,,"['-0.03378', '0.05478', '-0.01073', '-0.001086', '0.007446', '-0.0384', '0.002766', '0.04776', '-0.03555', '-0.04596', '-0.01689', '0.005096', '0.00924', '-0.01123', '-0.0154', '-0.0345', '-0.01497', '-0.01721', '-0.0693', '-0.1226', '-0.01062', '-0.05338', '0.0746', '-0.00861', '0.04276', '-0.01686', '-0.003067', '-0.007504', '-0.0071', '-0.03748', '0.0604', '0.005535', '0.0655', '0.03183', '-0.01019', '-0.04608', '-0.02382', '-0.01978', '-0.01825', '-0.07245', '0.02284', '-0.05142', '0.01947', '-0.02307', '0.01651', '-0.05304', '0.001214', '0.01958', '0.02322', '0.0479', '-0.02393', '-0.03714', '0.01252', '0.02115', '-0.04315', '-0.006878', '0.0537', '-0.04056', '-0.0769', '0.02797', '0.04373', '0.03012', '0.01236', '0.009224', '0.0309', '0.01443', '0.05722', '0.03192', '-0.06165', '0.0764', '-0.05106', '-0.00529', '-0.003271', '-0.0459', '0.0411', '0.01863', '0.01616', '-0.01064', '-0.0167', '-0.02615', '-0.02188', '-0.01357', '-0.0253', '0.03503', '-0.004177', '-0.013824', '0.02689', '0.0557', '0.08026', '0.007484', '0.0465', '0.05658', '-0.01105', '0.00565', '0.1329', '0.04907', '0.02914', '-0.10956', '-0.01724', '0.03117']",,,C562875,279.8,,,
mondo:0012351,zygodactyly type 1,"['ZYGODACTYLY 1', 'Zd1', 'SD1, Weidenreich type', 'Zygodactyly, Weidenreich type', 'syndactyly type 1a', 'zygodactyly type 1', 'SD1a', 'syndactyly type 1, Weidenreich type']",0111820,609815,295187,C1853294,,,,C565223,,,,
mondo:0012352,"vasculitis, lymphocytic, cutaneous small vessel","['vasculitis, lymphocytic, cutaneous small vessel']",,609817,,C1853293,,,,C565222,,,,
mondo:0012353,"erythrocytosis, familial, 3","['familial polycythemia caused by mutation in EGLN1', 'ECYT3', 'EGLN1 familial polycythemia', 'erythrocytosis, familial, 3', 'erythrocytosis, familial, type 3']",0080338,609820,,C1853286,,,,C565221,,,,
mondo:0012354,platelet-type bleeding disorder 8,"['bleeding disorder due to P2Ry12 defect', 'P2Y12 defect', 'ADP platelet receptor P2Y12 defect', 'bleeding disorder, platelet-type, 8', 'bleeding disorder due to P2Rx1 defect, somatic', 'BDPLT8', 'bleeding disorder, platelet-type 8']",0060692,609821,36355,C1853278,"['-0.926', '-0.4358', '-0.2148', '-0.4287', '-0.1669', '0.0797', '-0.3794', '0.2644', '-0.134', '-0.0481', '0.07635', '0.1332', '0.2705', '0.064', '-0.159', '-0.05246', '0.2732', '0.1624', '0.0314', '-0.6255', '-0.1083', '0.03613', '0.3513', '-0.5303', '-0.1195', '-0.10565', '-0.07184', '0.3062', '0.2156', '-0.2585', '-0.0685', '0.05917', '0.3516', '0.39', '-0.3813', '-0.397', '-0.1448', '-0.4705', '-0.165', '-0.2068', '0.6304', '-0.434', '0.083', '-0.4836', '-0.3933', '-0.2869', '-0.2883', '-0.3533', '0.316', '0.1366', '0.3162', '-0.2646', '0.3162', '0.624', '-0.3352', '0.2496', '0.699', '0.3955', '-0.643', '-0.002367', '-0.10614', '0.1993', '-0.0284', '-0.3801', '0.338', '-0.11224', '-0.049', '0.02892', '-0.5', '0.1733', '-0.505', '-0.12256', '-0.3982', '-0.09875', '0.625', '0.3481', '0.7773', '0.0917', '0.4006', '0.2576', '-0.6187', '-0.2656', '0.5386', '0.4548', '-0.1365', '0.4412', '0.3418', '0.745', '0.3037', '-0.642', '0.2695', '0.9326', '0.235', '-0.163', '0.918', '0.6724', '0.4832', '-0.7085', '0.1098', '0.6104']",,,C565220,,,,
mondo:0012355,autosomal recessive nonsyndromic hearing loss 28,"['DFNB28', 'autosomal recessive nonsyndromic deafness caused by mutation in TRIOBP', 'TRIOBP autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 28', 'autosomal recessive deafness 28', 'deafness, autosomal recessive type 28', 'autosomal recessive nonsyndromic deafness 28', 'deafness, autosomal recessive 28']",0110486,609823,,C1853276,,C129023,,C565218,,,,
mondo:0012358,"leprosy, susceptibility to, 1","['leprosy, susceptibility to, 1', 'LPRS1', 'leprosy, Paucibacillary type, susceptibility to, 1', 'leprosy, paucibacillary type, susceptibility to']",,609888,,,,,,,,,,
mondo:0012359,combined immunodeficiency due to partial RAG1 deficiency,"['CID due to partial RAG1 deficiency', 'CID with expansion of gamma delta T cells', 'alpha/beta T-cell lymphopenia with gamma/DELTA T-cell expansion, severe CYTOMEGALOVIRUS infection, and autoimmunity', 'combined immunodeficiency with expansion of gamma delta T cells']",,609889,231154,C4510944,"['-0.1681', '0.493', '-0.2184', '-0.517', '-0.1658', '-0.1887', '0.2002', '-0.04654', '-0.06323', '-0.5356', '-0.1615', '-0.1382', '-0.00445', '-0.00985', '0.5757', '-0.2312', '-0.3914', '-0.8853', '-0.4333', '-0.9136', '-0.318', '-0.4558', '0.742', '-0.534', '0.1707', '0.09424', '-0.6387', '0.1656', '-0.189', '-0.6533', '-0.09674', '0.653', '0.919', '-0.1298', '0.1464', '0.05463', '-0.3865', '-0.3', '-0.722', '-0.2876', '-0.2505', '0.08124', '0.5522', '-0.437', '-0.5176', '-0.2294', '-0.161', '-0.9585', '0.2424', '0.3296', '0.4805', '-0.5356', '0.91', '0.3389', '-0.4954', '0.2262', '0.1995', '-0.2656', '-0.0708', '0.4268', '0.01648', '0.2288', '-0.1247', '-0.4187', '0.7944', '-0.2379', '0.9443', '0.2505', '-0.3047', '0.861', '0.2551', '-0.1009', '-0.2089', '-0.4197', '0.7417', '-0.234', '-0.11163', '-0.01842', '0.352', '0.9136', '-0.2389', '-0.1494', '-0.1168', '-0.1326', '0.2249', '-0.2734', '0.9595', '0.8306', '0.321', '0.2069', '0.4775', '0.12115', '0.1893', '0.068', '0.7573', '0.7114', '-0.01041', '-0.5913', '0.3516', '-0.2712']",,,C563691,,,,
mondo:0012360,congenital nongoitrous hypothryoidism 3,"['resistance to thyrotropin', 'hypothyroidism, congenital, nongoitrous, 3', 'CHNG3', 'congenital nongoitrous hypothyroidism 3', 'thyrotropin resistance']",0070127,609893,,C2940785,,,,C567935,,,,
mondo:0012361,"systemic lupus erythematosus, susceptibility to, 5","['systemic lupus erythematosus, susceptibility to, 5', 'SLEB5']",,609903,,,,,,,,,,
mondo:0012362,dilated cardiomyopathy 1P,"['cardiomyopathy, dilated, type 1P', 'CMD1P', 'PLN familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 1P', 'familial isolated dilated cardiomyopathy caused by mutation in PLN', 'cardiomyopathy, dilated, 1P']",0110439,609909,,C1835928,,,,C563690,,,,
mondo:0012363,retinitis pigmentosa 32,"['retinitis pigmentosa 32', 'retinitis pigmentosa type 32', 'RP32']",0110355,609913,,C1835927,,,,C563689,,H35.5,,
mondo:0012364,dilated cardiomyopathy 1Q,"['cardiomyopathy, dilated, 1Q', 'dilated cardiomyopathy type 1Q', 'CMD1Q']",0110442,609915,,C1835926,,,,C563688,,,,
mondo:0012365,gallbladder disease 2,"['gallbladder disease 2', 'GBD2']",,609918,,C1835925,,,,C563687,,,,
mondo:0012366,gallbladder disease 3,"['GBD3', 'gallbladder disease 3']",,609919,,C1835924,,,,C563686,,,,
mondo:0012367,retinitis pigmentosa 31,"['retinitis pigmentosa type 31', 'TOPORS retinitis pigmentosa', 'RP 31', 'RP31', 'retinitis pigmentosa 31', 'retinitis pigmentosa caused by mutation in TOPORS']",0110391,609923,,C1835923,,,,C563685,,H35.5,,
mondo:0012368,aminoacylase 1 deficiency,"['ACY1 deficiency', 'ACY1D', 'N-acyl-L-amino acid amidohydrolase deficiency', 'aminoacylase 1 deficiency', 'neurological conditions associated with aminoacylase 1 deficiency', 'deficiency of the aminoacylase-1 enzyme']",,609924,137754,C1835922,"['-0.007866', '0.4648', '-0.1584', '0.1055', '0.284', '-0.2932', '-0.225', '1.085', '-0.6846', '0.2527', '-0.226', '-0.3582', '0.11475', '-0.3552', '0.2466', '0.171', '0.2795', '0.343', '-0.552', '-0.7686', '-0.1283', '-0.2852', '0.366', '0.05215', '0.09845', '-0.3193', '0.05606', '-0.1455', '0.3245', '0.3755', '0.357', '-0.344', '0.3108', '0.07715', '-0.2109', '-0.0619', '-0.38', '-0.2773', '0.005302', '0.313', '0.448', '-0.893', '0.3032', '-0.4758', '-0.2057', '-0.4111', '-0.0007644', '-0.2737', '-0.1996', '0.255', '-0.1589', '-0.1179', '-0.4497', '-0.11633', '-0.02946', '-0.1698', '0.1219', '-0.2822', '-0.424', '0.01952', '0.4148', '-0.1509', '0.8486', '-0.05765', '0.3105', '-0.07776', '0.06', '0.1857', '-0.2224', '0.2289', '-0.3823', '0.00889', '-0.3916', '0.2029', '0.2274', '0.45', '0.1831', '-0.2094', '-0.211', '-0.0717', '0.621', '0.3801', '0.0607', '0.528', '0.1355', '0.365', '0.02502', '0.2563', '0.3545', '0.4226', '0.7534', '0.2515', '-0.3474', '-0.467', '0.6206', '0.7876', '0.3176', '-0.791', '0.1809', '0.0609']",,1001981,C538246,270.8,,,
mondo:0012369,"systemic lupus erythematosus, susceptibility to, 6","['SLEB6', 'systemic lupus erythematosus, susceptibility to, 6']",,609939,,,,,,,,,,
mondo:0012370,autosomal recessive nonsyndromic hearing loss 51,"['autosomal recessive nonsyndromic deafness 51', 'deafness, autosomal recessive 51', 'autosomal recessive nonsyndromic deafness type 51', 'DFNB51', 'autosomal recessive deafness 51']",0110508,609941,,,,,,C538202,,,,
mondo:0012371,Noonan syndrome 3,"['Noonan syndrome caused by mutation in KRAS', 'NS3', 'KRAS Noonan syndrome', 'Noonan syndrome type 3', 'KRAS gene related Noonan syndrome', 'Noonan syndrome 3']",0060581,609942,,C1860991,,C176931,,C537847,,,,
mondo:0012373,"ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features","['ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features']",,609944,,C1864966,,,,C536182,,,,
mondo:0012374,"brachyphalangy, polydactyly, and tibial aplasia/hypoplasia","['brachyphalangy, polydactyly and absent tibiae', 'brachyphalangy, polydactyly, and tibial aplasia/hypoplasia']",,609945,,C1864965,,,,C537100,,,,
mondo:0012375,autosomal recessive nonsyndromic hearing loss 47,"['autosomal recessive nonsyndromic deafness 47', 'deafness, autosomal recessive 47', 'DFNB47', 'autosomal recessive nonsyndromic deafness type 47', 'autosomal recessive deafness 47', 'deafness, neurosensory, autosomal recessive 47']",0110504,609946,,C1864964,,,,C566498,,,,
mondo:0012376,autosomal recessive nonsyndromic hearing loss 55,"['autosomal recessive nonsyndromic deafness 55', 'autosomal recessive deafness 55', 'DFNB55', 'autosomal recessive nonsyndromic deafness type 55', 'deafness, autosomal recessive 55']",0110510,609952,,,,,,C538203,,,,
mondo:0012377,"asperger syndrome, susceptibility to, 4","['ASPG4', 'ASPERGER syndrome, susceptibility to, 4', 'Asperger syndrome susceptibility 4']",,609954,,,,,,,,,,
mondo:0012378,"fibromatosis, gingival, 3","['HGF3', 'hereditary gingival fibromatosis, 3', 'fibromatosis, gingival, 3', 'GINGF3', 'fibromatosis, gingival, hereditary, 3', 'gingival fibromatosis, 3', 'GGF3', 'fibromatosis gingival, hereditary, 3']",,609955,,,,,,C537928,,,,
mondo:0012379,"asthma-related traits, susceptibility to, 3","['ASRT3', 'asthma-related traits, susceptibility to, type 3', 'asthma-related traits, susceptibility to, 3']",,609958,,,,,,,,,,
mondo:0012380,autosomal dominant nonsyndromic hearing loss 53,"['autosomal dominant nonsyndromic deafness type 53', 'deafness, autosomal dominant nonsyndromic sensorineural 53', 'autosomal dominant nonsyndromic deafness 53', 'autosomal dominant deafness 53', 'DFNA53', 'deafness, autosomal dominant 53']",0110579,609965,,C1864957,,,,C566495,,,,
mondo:0012381,hyperinsulinism due to INSR deficiency,"['hyperinsulinemic hypoglycemia due to insulin receptor deficiency', 'hyperinsulinemic hypoglycemia due to INSR deficiency', 'hyperinsulinemic hypoglycemia, familial, 5', 'HHF5', 'hyperinsulinemic hypoglycemia, familial, type 5']",0070220,609968,263458,C1864952,"['-0.41', '0.323', '-0.4495', '0.1344', '-0.05148', '-0.2439', '-0.04462', '0.298', '-0.0909', '-0.1293', '-0.0759', '0.3704', '-0.01311', '-0.334', '-0.03845', '0.1589', '0.0775', '0.1469', '-0.1246', '-0.519', '0.1362', '-0.11334', '0.1854', '0.0457', '-0.2727', '0.2452', '0.1251', '-0.3635', '-0.0799', '-0.7324', '0.633', '0.224', '0.3735', '0.133', '-0.4312', '-0.00855', '-0.323', '-0.1104', '-0.212', '-0.2158', '-0.002823', '-0.5933', '0.5903', '-0.097', '-0.2703', '-0.318', '-0.2035', '0.2361', '-0.11743', '0.4124', '0.10474', '-0.05124', '-0.043', '-0.11053', '-0.094', '-0.1831', '0.3604', '-0.3127', '-0.4275', '0.2444', '0.2241', '-0.01417', '0.3872', '-0.63', '0.204', '-0.0403', '0.2356', '0.3572', '-0.7153', '0.1617', '-0.1525', '0.1222', '0.216', '-0.03452', '0.4626', '0.2876', '-0.0722', '0.0599', '-0.0838', '0.02919', '0.10504', '0.517', '-0.2627', '-0.1786', '0.6387', '0.3823', '0.08716', '-0.004574', '0.7153', '0.0557', '0.2235', '0.319', '-0.03955', '-0.2842', '0.782', '0.0919', '0.546', '-0.6094', '-0.378', '0.0679']",,,C566494,,,,
mondo:0012382,"hyperinsulinemic hypoglycemia, familial, 4","['M-SCHAD deficiency', 'HHF4', '3-alpha hydroxyacyl-CoA dehydrogenase deficiency', '3-Alpha-hydroxyacyl-Coenzyme A dehydrogenase deficiency', 'SCHAD deficiency, formerly', 'hyperinsulinemic hypoglycemia due to HADH deficiency', 'HADH deficiency', 'M/SCHAD', '3-hydroxyacyl-Coenzyme A dehydrogenase deficiency', 'HADH hyperinsulinemic hypoglycemia (disease)', 'hyperinsulinemic hypoglycemia, familial, 4', '3-hydroxyacyl-CoA dehydrogenase deficiency', 'SCHAD deficiency', 'hyperinsulinism due to SCHAD deficiency', 'hyperinsulinism due to glutamodehydrogenase deficiency', 'HADHSC deficiency', '3-hydroxylacyl-CoA dehydrogenase deficiency', 'had deficiency', 'L-3-Alpha-hydroxyacyl-CoA dehydrogenase, short chain, deficiency', 'medium and short chain 3-hydroxyacyl-CoA dehydrogenase deficiency', 'hyperinsulinemic hypoglycemia due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency', 'hyperinsulinemic hypoglycemia, familial, type 4', 'hyperinsulinism due to short chain 3-hydroxylacyl-CoA dehydrogenase deficiency']",0070215,609975,71212,C4303473,"['0.178', '0.0746', '0.07794', '0.628', '-0.4182', '-0.06665', '-0.3071', '0.571', '0.1384', '-0.2676', '0.0645', '0.01531', '0.2593', '0.8213', '-0.6064', '0.03482', '-0.2468', '-0.014534', '-0.497', '0.09064', '0.05676', '-0.374', '-0.4346', '0.10596', '-0.635', '-0.5737', '-0.6416', '-0.4766', '0.1007', '-0.5986', '0.665', '0.2747', '-0.0899', '-0.154', '-0.7427', '0.389', '-0.354', '0.2734', '0.139', '-0.26', '0.1747', '-0.4177', '-0.4763', '0.2573', '-0.092', '-0.4321', '-0.0009527', '-0.2996', '-0.1517', '0.7026', '0.497', '0.3142', '0.432', '0.09955', '-0.0366', '0.1323', '0.1583', '0.1154', '-0.866', '0.571', '-0.02318', '0.5605', '0.519', '-0.7563', '-0.6904', '-0.1219', '0.05295', '0.1371', '-0.7915', '0.2064', '-0.1407', '0.73', '0.293', '-0.5557', '-0.1913', '0.924', '0.00817', '0.5083', '-0.03014', '0.385', '-0.0918', '0.5747', '-0.659', '0.2178', '0.1061', '-0.0174', '-0.0723', '-0.2239', '1.223', '0.1554', '0.1783', '-0.0736', '0.03827', '0.03812', '0.862', '0.4512', '-0.01118', '-0.8823', '-0.06433', '0.8423']",,,C566493,,,,
mondo:0012383,primary immunodeficiency with natural-killer cell deficiency and adrenal insufficiency,"['NKGCD', 'mini-chromosome maintenance 4', 'IMD54', 'natural Killer cell deficiency, familial isolated', 'natural KILLER cell and glucocorticoid deficiency with DNA repair defect', 'immunodeficiency 54', 'primary immunodeficiency due to MCM4 deficiency']",0111967,609981,75391,C1864947,"['-0.2747', '0.0691', '0.02649', '0.4185', '0.782', '0.2053', '0.3884', '0.00267', '-0.02414', '-0.03262', '0.2546', '0.01875', '-0.3245', '0.3184', '0.492', '0.3225', '-0.2908', '0.6113', '-1.086', '-0.4595', '0.443', '0.4023', '0.2046', '-0.2157', '0.271', '-0.633', '-0.827', '-0.395', '0.11914', '-0.7876', '0.237', '0.5415', '0.1155', '-0.53', '-0.2352', '0.341', '-0.583', '-0.1307', '-0.2214', '-0.07654', '0.2842', '0.1537', '-0.165', '-0.3945', '-0.1467', '-0.863', '-0.0826', '-0.02481', '0.2925', '0.02188', '-0.3235', '-0.2338', '0.31', '-0.1005', '-0.3965', '0.02611', '-0.796', '0.0583', '-0.2461', '-0.2274', '-0.0515', '0.604', '0.0799', '0.3945', '0.639', '0.2583', '0.0368', '0.829', '-0.3257', '0.6074', '0.0191', '0.0622', '-0.1998', '-0.2786', '0.2467', '-0.010475', '-0.317', '-0.002705', '0.359', '0.57', '-0.2349', '0.3745', '0.06216', '0.261', '-0.0195', '0.1642', '0.5957', '0.6313', '0.896', '0.3257', '-0.1829', '0.4844', '-0.2957', '-0.3335', '0.524', '1.162', '-0.1197', '-0.962', '-0.08875', '0.03708']",C123729,,C566492,,,,
mondo:0012384,panic disorder 3,"['panic disorder susceptibility locus, chromosome 4Q-related', 'Pand3', 'panic disorder 3', 'panic disorder type 3']",,609985,,C1864946,,,,,,,,
mondo:0012385,"metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands","['cupped metaphyses and cone-Shaped epiphyses without alopecia or brachydactyly', 'metaphyseal chondrodysplasia with cone-shaped epiphyses, normal hair, and normal hands']",,609989,,C1864944,,,,C537354,,,,
mondo:0012386,trichoscyphodysplasia,"['metaphyseal chondrodysplasia with ectodermal dysplasia', 'Trichoscyphodysplasia', 'cupped metaphyses and cone-Shaped epiphyses with alopecia', 'metaphyseal chondrodysplasia with cone-Shaped epiphyses and alopecia']",,609990,,C1864943,,,,C536557,,,,
mondo:0012387,osteosclerosis-ichthyosis-premature ovarian failure syndrome,"['osteosclerosis with ichthyosis and premature ovarian failure', 'sclerosing dysplasia of bone-ichthyosis-premature ovarian failure syndrome', 'osteosclerosis with ichthyosis and POF', 'sclerosing dysplasia of bone with ichthyosis and premature ovarian failure']",,609993,75325,,,,,C536064,,,,
mondo:0012388,"myopia 11, autosomal dominant","['myopia 11, autosomal dominant', 'MYP11', 'myopia 11']",,609994,,C1864941,,,,C566490,,,,
mondo:0012389,"myopia 12, autosomal dominant","['myopia 12, autosomal dominant', 'myopia 12', 'MYP12']",,609995,,C1864940,,,,C566489,,,,
mondo:0012390,"arthrogryposis multiplex with deafness, inguinal hernias, and early death","['arthrogryposis multiplex with deafness, inguinal hernias, and early death']",,610001,,C1864939,,,,C535381,,,,
mondo:0012391,neuronal ceroid lipofuscinosis 8 northern epilepsy variant,"['NCL, Northern epilepsy variant', 'progressive epilepsy with mental retardation, northern epilepsy', 'CLN8 disease, EPMR (subtype)', 'neuronal ceroid lipofuscinosis 8', 'epilepsy mental deterioration Finnish type', 'CLN8 disease, Northern epilepsy variant', 'ceroid lipofuscinosis, neuronal, 8, NORTHERN epilepsy variant', 'CLN8 disease, late infantile (subtype)', 'progressive epilepsy - intellectual disability, Finnish type', 'CLN8', 'epilepsy, progressive, with mental retardation', 'neuronal ceroid lipofuscinosis, Northern epilepsy variant', 'Northern epilepsy', 'progressive epilepsy-intellectual disability syndrome, Finnish type', 'EPMR', 'progressive epilepsy with intellectual disability, northern epilepsy', 'northern epilepsy variant, neuronal ceroid lipofuscinosis, Northern epilepsy variant', 'ceroid lipofuscinosis neuronal 8', 'epilepsy, progressive, with intellectual disability']",0110724,610003,1947,,"['0.791', '0.1715', '-0.448', '-0.1084', '-0.4326', '-0.505', '0.403', '0.009', '-0.3308', '-0.3623', '-0.2568', '-0.1559', '-0.1449', '0.256', '0.2269', '-0.1704', '-0.3733', '-0.524', '-0.317', '-0.177', '-0.06116', '0.2656', '-0.3054', '-0.3064', '-0.3218', '-0.0652', '-0.1478', '-0.3303', '-0.8706', '0.5903', '0.3374', '-0.7417', '0.3901', '0.1138', '0.8535', '0.2778', '-0.1838', '0.4038', '0.01735', '-0.2386', '-0.3206', '-0.5996', '0.1974', '-0.2241', '-0.4001', '-0.8525', '-0.1055', '0.11395', '0.3384', '0.535', '0.2026', '0.1432', '-0.129', '-0.312', '0.0951', '-0.644', '0.002958', '0.1809', '-0.4648', '0.25', '-0.566', '0.2983', '0.4417', '-0.372', '0.1427', '1.254', '0.469', '0.1724', '-0.7827', '0.3018', '0.4834', '0.6997', '-0.04462', '-0.651', '0.2578', '0.4336', '0.782', '0.10767', '-0.675', '0.4387', '0.3271', '0.559', '0.01675', '0.2026', '0.555', '0.02992', '0.2734', '0.715', '0.062', '0.76', '0.0007267', '0.1752', '-0.3066', '0.2081', '0.226', '0.10474', '0.4504', '-0.3958', '0.7363', '0.1995']",,,,,,,
mondo:0012392,2-methylbutyryl-CoA dehydrogenase deficiency,"['2-methylbutyryl Glycinuria', 'butyryl-CoA dehydrogenase deficiency', 'short/branched-chain acyl-coA dehydrogenase deficiency', 'short branched-chain acyl-CoA dehydrogenase deficiency', 'short/branched-chain acyl-Coa dehydrogenase deficiency', '2-methylbutyrylglycinuria', '2-methylbutyric aciduria', 'SBCAD deficiency', 'developmental delay due to 2-methylbutyryl-CoA dehydrogenase deficiency', '2-methylbutyryl-CoA dehydrogenase deficiency']",,610006,79157,C1864912,"['-0.2317', '0.1815', '-0.0759', '-0.2686', '0.03378', '-0.1251', '-0.3867', '0.534', '-0.2173', '0.1263', '-0.1829', '-0.1372', '0.2072', '-0.2035', '-0.05414', '0.1451', '0.03656', '0.04092', '-0.3262', '-0.4863', '0.1498', '-0.2595', '0.2874', '0.1368', '0.1708', '-0.3076', '-0.004333', '-0.11365', '-0.2206', '-0.0944', '0.511', '-0.1309', '0.3926', '0.1954', '-0.2585', '-0.0629', '-0.10504', '-0.274', '-0.2361', '-0.4355', '-0.107', '-0.4724', '0.165', '-0.0387', '-0.585', '-0.05295', '0.01155', '-0.05295', '-0.07965', '0.4622', '-0.307', '-0.01694', '-0.08386', '-0.2715', '-0.198', '0.3274', '0.1868', '-0.407', '-0.359', '0.337', '0.2258', '-0.087', '0.1722', '-0.03897', '-0.01619', '-0.0816', '0.2915', '0.2356', '-0.5386', '0.1228', '-0.2786', '0.09814', '-0.316', '0.264', '0.2458', '0.06946', '0.1245', '-0.08575', '-0.2422', '-0.0209', '0.1903', '0.0825', '-0.0539', '0.05353', '0.239', '0.4456', '-0.324', '-0.02745', '0.4595', '-0.004063', '0.3315', '0.2417', '-0.2373', '-0.2338', '0.4912', '0.547', '0.02641', '-0.09595', '-0.3088', '-0.04407']",C98863,,C566487,,,,
mondo:0012393,congenital brain dysgenesis due to glutamine synthetase deficiency,"['glutamine synthetase deficiency, congenital systemic', 'inherited glutamine synthetase deficiency', 'glutamine deficiency, congenital', 'congenital glutamine deficiency', 'glutamine synthase deficiency, congenital systemic', 'inherited GS deficiency']",,610015,71278,C1864910,"['-0.2456', '0.2219', '-0.0609', '-0.2115', '0.2742', '-0.1105', '-0.1404', '0.2507', '-0.2913', '0.1021', '-0.3235', '-0.373', '-0.03613', '-0.2385', '-0.1322', '-0.1532', '0.1547', '-0.1094', '-0.4258', '-0.5195', '0.1748', '-0.1716', '0.3167', '-0.2234', '0.1979', '-0.2827', '0.06915', '0.2228', '-0.1533', '-0.1598', '0.3496', '0.206', '0.632', '0.263', '-0.0084', '0.2496', '-0.2603', '0.1122', '-0.1432', '-0.076', '0.10693', '-0.348', '-0.02112', '0.188', '-0.169', '-0.2394', '0.12115', '0.1785', '-0.12445', '0.1362', '0.1475', '0.00839', '0.0918', '-0.1738', '-0.4092', '-0.1439', '0.1311', '-0.2864', '-0.1896', '0.2542', '-0.0377', '0.0887', '0.0444', '-0.05347', '-0.3062', '-0.0771', '0.5874', '0.349', '-0.434', '0.119', '-0.3015', '0.3499', '-0.093', '0.06604', '-0.3083', '-0.1263', '0.453', '-0.1393', '-0.1412', '-0.06525', '-0.05557', '0.11456', '-0.02753', '0.2003', '0.10944', '-0.0349', '-0.10254', '0.2642', '0.3071', '0.01428', '0.4397', '0.505', '0.05304', '0.1859', '-0.0457', '0.5225', '0.2625', '-0.0667', '0.5156', '0.405']",,,C536832,,,,
mondo:0012394,multiple synostoses syndrome 2,"['SYNS2', 'multiple synostoses syndrome type 2', 'multiple synostoses syndrome caused by mutation in GDF5', 'GDF5 multiple synostoses syndrome', 'multiple synostoses syndrome 2']",0081318,610017,,C1832708,,,,C537380,,,,
mondo:0012395,cataract 18,"['cataract 18 autosomal recessive', 'cataract 18', 'CTRCT18', 'cataract type 18', 'CATC2', 'cataract 18, autosomal recessive', 'autosomal recessive congenital cataract 2', 'FYCO1 cataract (disease)', 'cataract, autosomal recessive congenital 2']",0110238,610019,,,,,,C535337,,,,
mondo:0012396,exercise-induced hyperinsulinism,"['hyperinsulinism due to monocarboxylate transporter 1 deficiency', 'hyperinsulinemic hypoglycemia familial 7', 'exercise-induced hyperinsulinemic hypoglycemia', 'MCT1 hyperinsulinism', 'hyperinsulinism due to SLC16A1 deficiency', 'monocarboxylate transporter 1 hyperinsulinism', 'hyperinsulinemic hypoglycemia, exercise-induced', 'exercise induced hyperinsulinemic hypoglycemia', 'hyperinsulinemic hypoglycemia, familial, type 7', 'EIHI', 'hyperinsulinemic hypoglycemia, familial, 7', 'hyperinsulinemic hypoglycemia exercise-induced', 'HHF7']",0070214,610021,165991,C1864904,"['-0.6265', '0.6553', '-0.4849', '0.3174', '-0.02687', '-0.3853', '0.3906', '0.445', '0.1644', '-0.4685', '-0.05664', '0.2063', '0.1328', '-0.6533', '-0.10486', '0.149', '0.3171', '-0.2107', '-0.3508', '-0.375', '0.4355', '-0.1285', '0.4744', '0.0457', '-0.1109', '0.0538', '0.1881', '-0.2266', '-0.1985', '-0.144', '0.4565', '0.5', '0.0786', '-0.002657', '-0.485', '-0.09454', '-0.1998', '-0.01886', '-0.257', '0.004738', '0.11', '-0.5786', '0.2583', '0.04956', '-0.4724', '0.06854', '-0.1312', '-0.271', '0.695', '0.6787', '-0.1772', '-0.62', '-0.0937', '0.1174', '-0.02158', '-0.0381', '0.7163', '-0.6367', '-0.0905', '0.1583', '0.2299', '0.35', '0.1152', '-0.2319', '-0.004345', '0.07556', '0.10297', '0.3296', '-0.6265', '0.1938', '-0.03114', '0.2244', '0.1306', '0.11755', '0.272', '0.364', '0.2014', '0.1255', '-0.2668', '0.000998', '-0.1852', '0.01466', '0.03394', '-0.3142', '0.1427', '0.04468', '-0.2057', '0.0806', '0.6196', '0.00532', '0.572', '0.0435', '-0.0518', '-0.3948', '0.6094', '0.089', '0.11884', '-0.7373', '-0.4722', '0.3323']",C131839,,C538376,,,,
mondo:0012397,"brachydactyly, coloboma, and anterior segment dysgenesis","['brachydactyly, coloboma, and anterior segment dysgenesis']",,610023,,C1864901,,,,C566484,,,,
mondo:0012398,retinal cone dystrophy 3A,"['retinal cone dystrophy 3A', 'cone dystrophy with night blindness and supernormal rod responses PDE6H-related', 'retinal cone dystrophy 3', 'retinal cone dystrophy type 3A', 'cone dystrophy with night blindness and supernormal Rod responses, Pde6H-related', 'RCD3A', 'achromatopsia 6']",0081025,610024,,C1864900,,,,C566483,,,,
mondo:0012399,complex cortical dysplasia with other brain malformations 7,"['polymicrogyria, symmetric or asymmetric', 'cortical dysplasia, COMPLEX, with OTHER brain malformations 7', 'cortical dysplasia, Complex, with Other brain malformations 7', 'complex cortical dysplasia with other brain malformations caused by mutation in TUBB2B', 'polymicrogyria due to TUBB2B mutation', 'CDCBM7', 'TUBB2B complex cortical dysplasia with other brain malformations', 'PMGYSA', 'complex cortical dysplasia with other brain malformations type 7']",0090132,610031,300573,CN203403,"['-0.3132', '0.3323', '0.1449', '-0.3599', '-0.1396', '-0.264', '0.01918', '0.286', '-0.584', '-0.1938', '-0.3855', '-0.4546', '-0.1876', '-0.3179', '0.2686', '-0.10657', '0.1245', '-0.347', '-0.2861', '-0.4153', '0.184', '0.1318', '0.1771', '-0.0047', '0.2034', '-0.0609', '-0.0655', '0.157', '0.07166', '-0.0423', '0.1852', '0.01843', '0.6733', '0.0588', '0.1597', '0.0797', '-0.2098', '-0.2311', '-0.2292', '-0.2869', '0.2664', '-0.3308', '0.01616', '0.1858', '-0.03018', '-0.3145', '0.0936', '0.1923', '-0.04123', '-0.1311', '0.05026', '0.2196', '-0.1606', '0.05505', '-0.1798', '-0.1506', '0.3274', '0.1448', '-0.3674', '0.3652', '0.07355', '-0.01304', '0.4075', '0.1656', '-0.456', '0.2659', '0.4314', '0.2125', '-0.4883', '0.2944', '-0.324', '0.3875', '0.2142', '-0.07684', '-0.2189', '-0.1423', '0.6', '-0.1313', '-0.1109', '0.04843', '0.00728', '0.3088', '0.1404', '0.4927', '0.05667', '-0.3484', '0.05746', '0.625', '0.2878', '0.391', '0.2465', '0.4626', '0.12274', '-0.10706', '0.48', '0.1969', '0.595', '0.2083', '0.5312', '0.2039']",,,,,,,
mondo:0012400,cortical dysplasia-focal epilepsy syndrome,"['Pitt-Hopkins like syndrome 1', 'cortical dysplasia-focal epilepsy syndrome', 'Pitt-Hopkins-like syndrome 1', 'PTHSL1', 'CDFES', 'CDFE syndrome']",0090130,610042,163681,C1864887,"['0.861', '-0.0158', '-0.254', '-0.346', '-0.4333', '-0.3025', '0.767', '0.4377', '-0.6772', '-0.2893', '0.1599', '-0.10675', '-0.2705', '0.3032', '0.1857', '0.1305', '-0.1381', '-0.5444', '-0.4624', '-0.652', '-0.1522', '0.628', '0.268', '-0.4275', '0.005856', '-0.0735', '-0.10626', '-0.1257', '-0.7256', '0.1794', '0.367', '-0.7017', '0.2869', '0.3945', '0.7627', '0.5327', '-0.004326', '-0.1547', '-0.0962', '-0.2776', '-0.1238', '-0.439', '-0.02637', '-0.1407', '-0.4075', '-0.897', '-0.233', '0.2194', '0.4795', '0.556', '-0.134', '0.2266', '-0.167', '-0.5273', '0.4329', '-0.2197', '-0.1538', '-0.10956', '-0.1655', '0.617', '-0.7124', '0.499', '0.742', '-0.4482', '-0.3684', '1.231', '0.1464', '0.0002997', '-0.824', '0.6597', '0.798', '1.02', '-0.0906', '-0.1987', '0.0734', '0.68', '1.064', '0.2186', '-0.563', '0.2607', '-0.1211', '0.7627', '0.507', '0.2952', '0.10535', '0.259', '0.02737', '0.5244', '0.5938', '0.4932', '-0.1716', '0.3782', '-0.392', '-0.0382', '-0.02957', '0.1487', '0.653', '-0.434', '0.6406', '0.4114']",C133743,,C567657,,,,
mondo:0012401,congenital stromal corneal dystrophy,"['CSCD', 'congenital stromal corneal dystrophy', 'corneal dystrophy, congenital stromal', 'congenital hereditary stromal dystrophy', 'Witschel dystrophy']",0060445,610048,101068,C1864738,"['-0.3682', '-0.4792', '-0.4717', '0.3667', '0.4917', '-0.557', '-0.2708', '0.4968', '-0.1519', '-0.5713', '0.03445', '-0.2568', '-0.0163', '0.3057', '-0.3484', '-0.5073', '0.613', '-0.6094', '0.2041', '-0.7725', '-0.4304', '0.1714', '-0.10486', '0.1093', '-0.338', '0.3157', '-0.515', '0.1395', '-0.4302', '0.1744', '0.8843', '0.3953', '0.1794', '0.009964', '0.002407', '-0.3354', '-0.2476', '-0.6655', '0.1473', '0.06616', '0.5728', '-0.6597', '0.1427', '-0.1278', '-0.0811', '0.525', '-0.06964', '0.0788', '0.1344', '-0.0316', '0.6924', '-0.0945', '0.07947', '-0.406', '-0.1198', '0.2052', '0.3967', '-0.005863', '-0.982', '-0.2172', '0.1819', '-0.8394', '0.0897', '0.11554', '-0.0645', '-0.3484', '0.4048', '0.5894', '-0.578', '0.3716', '0.07104', '-0.3264', '0.3828', '0.07434', '0.762', '0.04944', '-0.1305', '0.2185', '-0.1775', '0.04974', '0.1283', '-0.1448', '-0.3704', '0.659', '0.03778', '-0.542', '-0.06525', '0.3003', '0.1288', '0.127', '0.06107', '0.5166', '0.0815', '0.3833', '0.2439', '0.07745', '0.3225', '-0.612', '0.3503', '0.1555']",,,C566452,371.56,,,
mondo:0012402,"opioid dependence, susceptibility to, 1","['Ods1', 'opioid dependence, susceptibility to, 1', 'opioid dependence, susceptibility to, type 1']",,610064,,,,,,,,,,
mondo:0012403,"systemic lupus erythematosus, susceptibility to, 7","['systemic lupus erythematosus, susceptibility to, 7', 'SLEB7']",,610065,,,,,,,,,,
mondo:0012404,"systemic lupus erythematosus, susceptibility to, 8","['systemic lupus erythematosus, susceptibility to, 8', 'SLEB8']",,610066,,,,,,,,,,
mondo:0012405,"polyposis syndrome, hereditary mixed, 2","['hereditary mixed polyposis syndrome caused by mutation in BMPR1A', 'polyposis syndrome, hereditary mixed, 2', 'HMPS2', 'polyposis syndrome, hereditary mixed, type 2', 'BMPR1A hereditary mixed polyposis syndrome']",0111686,610069,,C1864730,,,,C566451,,,,
mondo:0012406,hyperparathyroidism 3,"['hyperparathyroidism 3', 'HRPT3', 'hyperparathyroidism, familial isolated']",,610071,,C1864729,,,,C566450,,,,
mondo:0012407,pyridoxal phosphate-responsive seizures,"['pyridoxamine 5-prime-phosphate oxidase deficiency', 'pyridoxine-5^-phosphate oxidase deficiency', 'PNPOD', 'PNPO deficiency', 'pyridoxal phosphate-dependent seizures', 'pyridoxamine 5^-oxidase deficiency', 'epileptic encephalopathy, neonatal, Pnpo-related', 'pyridoxal 5^-phosphate-dependent epilepsy', 'Pnpo deficiency', 'pyridoxamine 5^-phosphate oxidase deficiency', 'seizures, pyridoxine-resistant, PLP-sensitive', 'PNPO-related neonatal epileptic encephalopathy', 'pyridoxine 5^ phosphate oxidase deficiency']",0111329,610090,79096,C1864723,"['0.0659', '-0.063', '-0.2404', '0.3372', '-0.618', '-0.5034', '0.7505', '0.2773', '-0.254', '-0.4736', '-0.2852', '-0.1919', '-0.1207', '0.6685', '-0.4424', '0.1632', '-0.05063', '-0.2954', '-0.1693', '-0.534', '-0.198', '0.5684', '-0.003027', '-0.3281', '0.0806', '-0.05753', '-0.07434', '-0.06143', '-0.3413', '0.597', '-0.1274', '-0.1141', '0.1487', '0.3943', '0.5127', '0.539', '-0.04703', '-0.3484', '-0.08856', '-0.4568', '-0.2045', '-0.3203', '-0.2874', '-0.49', '0.1835', '-0.605', '-0.1514', '0.4229', '0.2019', '1.0205', '0.0315', '0.02202', '0.2125', '-0.53', '0.1484', '0.2292', '0.04443', '0.0792', '-0.2365', '-0.1814', '-0.2595', '0.262', '0.5537', '-0.07104', '-0.7603', '1.175', '0.3472', '-0.2032', '-0.79', '0.816', '0.505', '0.4973', '0.12244', '-0.567', '0.5015', '0.8', '0.5835', '0.3545', '0.0132', '-0.1884', '0.0393', '0.917', '0.3223', '0.2256', '0.3828', '-0.1924', '0.03552', '0.949', '0.769', '1.058', '0.125', '0.3254', '0.06', '0.1274', '-0.07715', '0.1962', '0.05444', '-0.3083', '0.1687', '0.4668']",,,C566449,,,,
mondo:0012408,"microphthalmia, isolated, with coloboma 3","['microphthalmia, isolated, with coloboma 3', 'microphthalmia, colobomatous, isolated 3', 'microphthalmia, cataracts, and iris abnormalities', 'microphthalmia, isolated, with coloboma type 3', 'VSX2 microphthalmia, isolated, with coloboma', 'MCOPCB3', 'microphthalmia, isolated, with coloboma caused by mutation in VSX2', 'microphthalmia with coloboma 3']",,610092,,C1864721,,,,C566447,,,,
mondo:0012409,isolated microphthalmia 2,"['isolated microphthalmia type 2', 'VSX2 isolated microphthalmia', 'anophthalmia, clinical, isolated', 'MCOP2', 'microphthalmia, isolated 2', 'microphthalmia, isolated type 2', 'isolated microphthalmia caused by mutation in VSX2']",0060839,610093,,C1864720,,,,C566446,,,,
mondo:0012410,Finnish upper limb-onset distal myopathy,"['distal myopathy type 3', 'myopathy, distal, 3', 'MPD3']",0111189,610099,399086,C1864706,,,,,,,,
mondo:0012411,giant axonal neuropathy 2,"['DCAF8 giant axonal neuropathy', 'autosomal dominant Charcot-Marie-Tooth disease type 2 with giant axons', 'giant axonal neuropathy 2, autosomal dominant', 'CMT2 with giant axons', 'giant axonal neuropathy caused by mutation in DCAF8', 'GAN2', 'HMSN2 with giant axons', 'giant axonal neuropathy type 2', 'autosomal dominant hereditary motor and sensory neuropathy type 2 with giant axons']",0090069,610100,401964,CN226146,"['-0.4014', '0.4087', '0.1932', '-0.2141', '-0.329', '-0.3806', '-0.355', '0.1436', '-0.683', '0.5664', '-0.1943', '0.1251', '-0.08685', '-0.3215', '0.0755', '-0.2124', '-0.4165', '-0.05777', '0.1708', '-0.925', '0.132', '-0.2488', '0.2262', '0.702', '-0.08374', '0.464', '0.083', '0.2404', '-0.2365', '-0.2734', '0.2007', '-0.0505', '0.551', '0.2502', '0.262', '-0.626', '-0.3438', '-0.1594', '0.12305', '-0.727', '-0.9116', '-0.3516', '0.05185', '0.672', '-0.006744', '-0.4265', '0.07684', '0.2024', '-0.04254', '0.265', '0.1414', '0.2216', '-0.02205', '-0.2947', '0.1492', '-0.6973', '0.3835', '0.09753', '-0.2595', '0.06055', '-0.04837', '-0.11993', '0.3254', '0.5854', '-0.7954', '0.393', '0.1976', '0.6216', '-0.2769', '0.3877', '-0.779', '-0.06012', '0.2646', '-0.194', '0.916', '-0.1538', '-0.09985', '0.4883', '0.2886', '-0.3306', '0.1584', '-0.2457', '0.4424', '0.495', '-0.10547', '-0.1863', '0.02826', '0.6226', '0.4683', '-0.12067', '0.1658', '-0.2109', '0.356', '0.1571', '0.7275', '0.5796', '0.6045', '-0.0328', '-0.1746', '0.2229']",,,,,,,
mondo:0012412,complement component 7 deficiency,"['complement component 7 deficiency', 'classic complement early component deficiency caused by mutation in C7', 'C7D', 'C7 classic complement early component deficiency', 'C7 deficiency']",0060300,610102,,C1864694,,,,C566443,,,,
mondo:0012413,syndromic microphthalmia type 5,"['OTX2 syndromic microphthalmia', 'OTX2-related eye disorders', 'microphthalmia syndromic 5', 'retinal dystrophy, early-onset, with or without pituitary dysfunction', 'microphthalmia, syndromic type 5', 'microphthalmia, syndromic 5', 'MCOPS5', 'syndromic microphthalmia caused by mutation in OTX2', 'syndromic microphthalmia/anophthalmia due to OTX2 mutation']",0111806,610125,178364,C4305151,"['-0.4717', '-0.1039', '-0.04626', '0.2542', '0.3416', '0.0831', '0.2778', '0.3215', '-0.433', '-0.4043', '-0.1769', '-0.2886', '-0.2349', '-0.295', '-0.0906', '-0.1836', '0.469', '-0.1754', '-0.4585', '-0.2551', '0.3682', '0.2296', '0.03912', '-0.2507', '-0.01663', '-0.03934', '-0.2698', '0.1045', '0.2664', '0.04532', '0.689', '-0.305', '0.4368', '0.2292', '-0.0564', '-0.1798', '-0.2406', '-0.522', '-0.3953', '-0.105', '0.5093', '0.00233', '0.1426', '-0.3118', '-0.09906', '0.0837', '0.453', '-0.1969', '-0.2054', '-0.3875', '0.1227', '0.04584', '-0.4192', '0.0707', '-0.3655', '0.2998', '0.11804', '-0.4138', '-0.3428', '0.4216', '0.05093', '-0.411', '0.155', '0.303', '-0.542', '-0.0662', '0.1301', '1.165', '-0.6133', '-0.2546', '-0.3806', '0.4697', '-0.02142', '0.077', '0.3901', '-0.1991', '0.1332', '-0.06076', '0.001714', '-0.2357', '-0.01132', '0.49', '0.01042', '0.753', '-0.07306', '-0.3198', '0.2769', '0.4456', '0.5137', '0.0977', '0.2551', '0.6245', '0.1876', '-0.286', '0.9985', '0.08344', '0.3284', '-0.3972', '0.4194', '0.4563']",,,C566441,,,,
mondo:0012414,neuronal ceroid lipofuscinosis 10,"['CLN10 disease, juvenile (subtype)', 'neuronal ceroid lipofuscinosis due to Cathepsin D deficiency', 'CTSD neuronal ceroid lipofuscinosis', 'neuronal ceroid lipofuscinosis type 10', 'neuronal ceroid lipofuscinosis caused by mutation in CTSD', 'CLN10 disease', 'Cathepsin D deficiency', 'CLN10-NCL', 'ceroid lipofuscinosis neuronal Cathepsin D-deficient', 'CLN10 disease, congenital (subtype)', 'neuronal ceroid lipofuscinosis cathepsin D-deficient', 'CLN10', 'ceroid lipofuscinosis, neuronal, type 10', 'ceroid lipofuscinosis, neuronal, 10', 'CLN10 disease, late infantile (subtype)', 'neuronal ceroid lipofuscinosis, congenital', 'ceroid lipofuscinosis, neuronal, Cathepsin D-deficient', 'CLN10 disease, adult (subtype)', 'neuronal ceroid lipofuscinosis due to cathepsin D deficiency']",0110725,610127,228337,,"['-0.0565', '0.587', '-0.2136', '-0.11615', '-0.1194', '-0.5713', '-0.1517', '0.351', '-0.4343', '-0.467', '-0.2278', '0.11743', '-0.329', '0.01772', '0.3066', '0.0654', '-0.00919', '-0.158', '-0.1903', '-0.2737', '0.237', '-0.4429', '-0.2773', '-0.1533', '-0.013016', '-0.1204', '0.03094', '0.1577', '-0.3765', '0.1759', '0.06256', '0.05307', '0.03622', '0.126', '0.0788', '0.0691', '0.1991', '-0.1984', '-0.03735', '0.4531', '-0.0708', '-0.4275', '0.2487', '-0.09674', '-0.1947', '-0.1495', '-0.04837', '-0.04025', '0.1855', '0.168', '0.4148', '-0.1139', '-0.382', '-0.0704', '0.212', '-0.6343', '0.255', '-0.06027', '0.05685', '-0.1494', '0.0772', '0.3496', '0.428', '0.1317', '-0.10284', '0.3735', '0.401', '0.2708', '-0.4514', '0.02698', '-0.254', '0.2465', '0.07196', '-0.1786', '0.4338', '0.438', '0.04193', '0.2062', '-0.2922', '0.0007396', '0.12177', '0.11957', '-0.2727', '0.3596', '0.04117', '0.324', '0.3142', '0.02188', '0.3203', '0.2396', '-0.00886', '-0.0424', '-0.2866', '0.2527', '0.278', '0.3762', '0.4414', '-0.4958', '0.3052', '0.03918']",,,C566438,,,,
mondo:0012415,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4","['PEOA4', 'POLG2 progressive external ophthalmoplegia with mitochondrial DNA deletions', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 4', 'progressive external ophthalmoplegia, autosomal dominant 4', 'progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in POLG2', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 4']",0111525,610131,,C1864668,,,,C566437,,,,
mondo:0012416,Devriendt syndrome,"['severe short stature, hyperphalangy of the index fingers, mental retardation and facial dysmorphism', 'Devriendt syndrome', 'severe short stature, hyperphalangy of the index fingers, intellectual disability and facial dysmorphism']",,610136,,C1857830,,,,C535947,,,,
mondo:0012417,"heart-hand syndrome, Slovenian type","['atriodigital dysplasia, Slovenian type', 'Cardiac conduction disease-dilated cardiomyopathy-brachydactyly syndrome', 'heart-hand syndrome, Slovenian type']",,610140,168796,C1857829,"['-0.2778', '-0.1678', '-0.3784', '0.2598', '-0.1633', '-1.127', '0.1672', '0.667', '-0.127', '-0.6206', '-0.2803', '-0.309', '-0.486', '-0.2323', '-0.4395', '0.3064', '-0.3005', '0.1161', '0.04996', '-0.2903', '0.2922', '0.362', '0.000494', '-0.4844', '0.3494', '0.1744', '-0.1758', '0.284', '0.453', '-0.164', '0.336', '-0.3228', '0.0924', '0.2876', '0.111', '-0.832', '0.045', '-0.4346', '-0.1232', '-0.01494', '-0.1605', '-0.4434', '0.1564', '0.283', '0.152', '-0.04037', '-0.551', '0.6104', '-0.1299', '-0.319', '0.278', '0.08954', '-0.2125', '0.02654', '-0.1759', '-1.022', '0.06537', '-0.3186', '-0.1521', '0.2441', '0.11414', '-0.1974', '0.1599', '-0.1232', '-0.8525', '-0.10516', '0.1577', '0.925', '-0.7373', '-0.2301', '-0.09', '0.199', '0.2257', '-0.396', '0.6357', '0.311', '-0.432', '0.1311', '-0.3032', '0.10956', '0.577', '-0.246', '0.2747', '0.297', '0.5576', '0.1632', '-0.1503', '-0.0718', '0.4412', '-0.3289', '0.0676', '0.1498', '0.2837', '0.5728', '0.7144', '0.868', '0.7666', '-0.5825', '-0.4314', '0.143']",,,C535852,,,,
mondo:0012418,autosomal recessive nonsyndromic hearing loss 62,"['autosomal recessive nonsyndromic deafness type 62', 'DFNB62', 'autosomal recessive nonsyndromic deafness 62', 'deafness, autosomal recessive 62', 'autosomal recessive deafness 62']",0110514,610143,,C1857820,,,,C565719,,,,
mondo:0012419,age related macular degeneration 7,"['age related macular degeneration type 7', 'macular Degeneration, age-related, neovascular type, susceptibility to', 'HTRA1 age-related macular degeneration', 'macular degeneration, age-related, neovascular type', 'macular Degeneration, age-related, wet type, susceptibility to', 'macular degeneration, age-related, 7', 'age-related macular degeneration caused by mutation in HTRA1', 'macular Degeneration, age-related, type 7', 'ARMD7']",0110019,610149,,C1857813,,,,C565718,,,,
mondo:0012420,autosomal recessive nonsyndromic hearing loss 49,"['deafness, autosomal recessive 49', 'DFNB49', 'autosomal recessive nonsyndromic deafness 49', 'autosomal recessive deafness 49', 'autosomal recessive nonsyndromic deafness type 49', 'autosomal recessive nonsyndromic deafness caused by mutation in MARVELD2', 'MARVELD2 autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive type 49']",0110506,610153,,C1857811,,C129024,,C565717,,,,
mondo:0012421,autosomal recessive nonsyndromic hearing loss 44,"['DFNB44', 'deafness, autosomal recessive type 44', 'deafness, autosomal recessive 44', 'autosomal recessive nonsyndromic deafness 44', 'autosomal recessive nonsyndromic deafness type 44', 'autosomal recessive deafness 44', 'ADCY1 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness caused by mutation in ADCY1']",0110501,610154,,C1857809,,,,C565716,,,,
mondo:0012422,type 1 diabetes mellitus 19,"['IDDM19', 'insulin-dependent diabetes mellitus 19', 'diabetes mellitus, insulin-dependent, 19']",0110756,610155,,C1857808,,,,C565715,,,,
mondo:0012423,MORM syndrome,"['mental retardation, truncal obesity, retinal dystrophy, and micropenis syndrome', 'MORM syndrome', 'intellectual disability, truncal obesity, retinal dystrophy, and micropenis syndrome', 'MORMS', 'mental retardation-truncal obesity-retinal dystrophy-micropenis syndrome', 'intellectual disability, truncal obesity, retinal dystrophy and micropenis', 'mental retardation, truncal obesity, retinal dystrophy and micropenis', 'mental retardation, truncal obesity, retinal dystrophy, and micropenis', 'intellectual disability-truncal obesity-retinal dystrophy-micropenis syndrome']",,610156,75858,C1857802,"['-0.495', '0.1549', '-0.1104', '-0.1243', '0.2832', '-1.123', '0.07697', '0.6963', '-0.03598', '-0.6724', '-0.0759', '0.00989', '0.04672', '-0.2035', '0.2151', '-0.293', '0.4758', '0.04678', '-0.398', '-0.5854', '-0.173', '0.1444', '-0.1646', '0.000829', '0.1409', '-0.106', '-0.2341', '-0.1171', '0.01008', '-0.04288', '0.9365', '-0.2242', '-0.0549', '0.1445', '-0.03918', '0.03223', '0.1456', '-0.4622', '-0.11176', '-0.3298', '0.353', '0.2532', '-0.1862', '-0.01407', '-0.04654', '0.0904', '0.1276', '-0.1122', '-0.315', '-0.2369', '-0.001563', '0.2025', '-0.256', '-0.204', '0.544', '-0.1095', '0.8203', '-0.04996', '-0.3364', '0.1499', '0.112', '-0.2001', '0.337', '0.3801', '0.04858', '0.3374', '0.00885', '0.5913', '-0.5674', '0.2429', '-0.6104', '0.0697', '-0.00949', '-0.0892', '0.5234', '-0.1547', '0.00955', '-0.0558', '-0.2052', '0.2279', '0.2537', '0.4192', '0.0394', '0.6777', '0.0763', '0.1975', '-0.1403', '0.4368', '0.3958', '0.06946', '-0.2368', '1.033', '0.1605', '-0.0287', '0.7544', '-0.2915', '0.02148', '-0.5845', '0.3064', '-0.05374']",,,C536984,,,,
mondo:0012425,"corneal dystrophy, fuchs endothelial, 2","['Fcd1 locus', 'FECD2', 'corneal dystrophy, Fuchs endothelial, 2', 'corneal dystrophy, Fuchs endothelial, late-onset']",,610158,,C1857800,,,,C535479,,,,
mondo:0012426,immunodeficiency 25,"['CD3zeta deficiency', 'IMD25', 'immunodeficiency due to defect in CD3-zeta', 'immunodeficiency 25', 'CD247 severe combined immunodeficiency (disease)', 'immunodeficiency type 25']",0111942,610163,,C1857798,,,,C565712,,,,
mondo:0012427,Loeys-Dietz syndrome 2,"['TGFBR2 Loeys-Dietz syndrome', 'Loeys-Dietz syndrome 2', 'Marfan syndrome, type II', 'Loeys-Dietz syndrome type 2', 'aortic aneurysm, familial thoracic 3', 'Loeys-Dietz syndrome type II', 'Loeys-Dietz syndrome caused by mutation in TGFBR2', 'Marfan syndrome, type II, formerly', 'LDS2']",0070234,610168,91387,,,C114768,,C537783,,,,
mondo:0012428,kyphoscoliosis 1,"['kyphoscoliosis 1', 'KYPSC1']",,610170,,C1857795,,,,C565711,,,,
mondo:0012429,Aicardi-Goutieres syndrome 2,"['RNASEH2B-related Aicardi-Goutieres syndrome', 'Aicardi-Goutieres syndrome caused by mutation in RNASEH2B', 'RNASEH2B Aicardi-Goutieres syndrome', 'Aicardi-Goutieres syndrome type 2', 'AGS2', 'Aicardi-Goutieres syndrome 2']",,610181,,C3489724,,C165673,,,,,,
mondo:0012430,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2","['WDR81 dysequilibrium syndrome', 'cerebellar ataxia, mental retardation, and dysequilibrium syndrome 2', 'cerebellar ataxia and mental retardation with or without quadrupedal locomotion 2', 'CAMRQ2', 'cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 2', 'cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 2', 'cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 2', 'cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 2', 'dysequilibrium syndrome caused by mutation in WDR81']",,610185,,C2750234,,,,C567656,,,,
mondo:0012431,diaphragmatic hernia 3,"['congenital diaphragmatic hernia caused by mutation in ZFPM2', 'diaphragmatic hernia 3', 'DIH3', 'ZFPM2 congenital diaphragmatic hernia', 'diaphragmatic hernia type 3']",,610187,,,"['-0.03375', '0.0369', '0.03305', '-0.036', '0.065', '-0.0848', '-0.002449', '0.1356', '-0.0936', '-0.02989', '-0.0216', '-0.012596', '-0.0181', '0.014175', '-0.0753', '-0.004967', '-0.01932', '-0.0583', '-0.01129', '-0.1259', '-0.01942', '-0.011284', '0.07764', '-0.01917', '0.0212', '-0.004738', '0.004524', '0.02133', '0.07886', '-0.073', '0.09393', '-0.01892', '0.1252', '0.0483', '0.00802', '-0.06714', '-0.02219', '-0.03458', '0.01165', '-0.0881', '0.02837', '-0.0713', '0.01799', '-0.01956', '0.003016', '-0.02365', '-0.02489', '0.0669', '-0.05576', '0.02623', '-0.04657', '-0.01237', '-0.00608', '-0.00934', '-0.049', '-0.00935', '0.03946', '-0.0815', '-0.12244', '0.03102', '0.05783', '0.05545', '-0.02788', '0.0405', '0.0003877', '-0.02556', '0.09283', '0.0826', '-0.0626', '0.0948', '-0.081', '0.0408', '0.02345', '-0.07227', '0.03226', '-0.01556', '0.0654', '-0.002642', '-0.07605', '-0.0762', '-0.02122', '-0.007774', '0.02104', '0.0696', '-0.05408', '0.03293', '0.0239', '0.1113', '0.05276', '-0.03087', '0.0451', '0.0792', '0.03903', '0.02582', '0.2047', '0.00531', '0.0703', '-0.1005', '0.01607', '0.037']",,,C565710,,,,
mondo:0012432,Joubert syndrome 5,"['JBTS5', 'Joubert syndrome 5', 'CEP290 Joubert syndrome', 'Joubert syndrome caused by mutation in CEP290', 'Joubert syndrome type 5']",0111000,610188,,C1857780,,,,C537688,,,,
mondo:0012433,Senior-Loken syndrome 6,"['SLSN6', 'Senior-Loken syndrome type 6', 'CEP290 Senior-Loken syndrome', 'Senior-Loken syndrome caused by mutation in CEP290', 'Senior-Loken syndrome 6', 'SENIOR-Loken syndrome 6']",,610189,,C1857779,,,,C565708,,,,
mondo:0012434,arrhythmogenic right ventricular dysplasia 10,"['arrhythmogenic right ventricular cardiomyopathy caused by mutation in DSG2', 'ARVC10', 'familial arrhythmogenic right ventricular dysplasia 10', 'ARVD10', 'arrhythmogenic right ventricular dysplasia type 10', 'arrhythmogenic right ventricular cardiomyopathy 10', 'DSG2 arrhythmogenic right ventricular cardiomyopathy', 'arrhythmogenic right ventricular dysplasia, familial, 10', 'arrhythmogenic right ventricular dysplasia, familial, type 10']",0110081,610193,,C1857777,,,,C565707,,,,
mondo:0012435,3-methylglutaconic aciduria type 5,"['MGA5', 'dilated cardiomyopathy with ataxia', 'DCMA', 'cardiomyopathy, dilated, with ataxia', '3-methylglutaconic aciduria type 5', '3-METHYLGLUTACONIC aciduria, type V', 'DCMA syndrome', '3 alpha methylglutaconic aciduria type V', 'MGA 5', '3-methylglutaconic aciduria type V', 'Mga, type 5', '3-methylglutaconic aciduria caused by mutation in DNAJC19', '3 methylglutaconic aciduria type V', '3-Methylglutaconic aciduria, type 5', 'MGA V', 'MGCA5', 'DNAJC19 3-methylglutaconic aciduria']",0110000,610198,66634,C4039473,"['-0.4473', '0.0545', '-0.06006', '-0.1018', '0.467', '-0.6084', '-0.2576', '0.6807', '-0.1403', '-0.1711', '0.03458', '0.1772', '-0.2786', '-0.3845', '-0.0812', '-0.3733', '-0.3054', '-0.0882', '-0.3984', '-0.163', '0.0703', '0.2424', '0.0763', '-0.11536', '0.1713', '-0.1396', '0.418', '0.5127', '0.11053', '-0.564', '0.3557', '-0.1234', '0.4775', '0.02165', '-0.4062', '-0.357', '-0.2559', '-0.2377', '-0.6655', '0.05457', '-0.1893', '-0.3872', '0.6274', '0.17', '-0.2468', '-0.2793', '0.1562', '0.2224', '0.04977', '-0.1158', '-0.01559', '-0.2903', '-0.6416', '-0.02509', '0.061', '0.0713', '0.645', '-0.1595', '-0.3027', '0.2112', '0.0525', '-0.2019', '0.6045', '0.2261', '-0.3904', '-0.07697', '0.2578', '0.45', '-0.3313', '0.1337', '-0.12067', '0.394', '0.321', '0.1696', '-0.2203', '0.04623', '0.856', '-0.4897', '0.035', '0.2491', '0.2059', '0.05197', '-0.2966', '0.01866', '0.2257', '0.2445', '0.2102', '0.4236', '0.1327', '-0.317', '0.2637', '0.587', '-0.01345', '-0.1344', '0.6646', '0.11053', '0.6665', '-0.1105', '0.05847', '0.1406']",C173146,,C565706,,,,
mondo:0012436,neonatal diabetes mellitus with congenital hypothyroidism,"['Ndh syndrome', 'neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome', 'NDH syndrome', 'NDH', 'diabetes mellitus, neonatal, with congenital hypothyroidism']",0060638,610199,79118,C1857775,"['0.825', '-0.2202', '0.2219', '0.767', '-0.38', '-0.7974', '-0.3848', '0.997', '0.05423', '-0.6577', '0.204', '-0.1956', '0.2361', '0.1355', '-1.013', '-0.3933', '0.484', '0.328', '-0.1375', '-0.657', '0.3464', '-0.0531', '0.01617', '0.0725', '-0.703', '-0.3708', '0.1412', '0.1014', '0.58', '-0.41', '0.957', '-0.3787', '0.1732', '-0.2384', '-0.1262', '0.4763', '-0.7964', '0.3792', '-0.005814', '-0.1533', '0.1672', '0.567', '0.1295', '0.4731', '-0.4932', '-0.4392', '0.541', '-0.0959', '-0.07513', '0.264', '0.298', '-0.3242', '0.803', '-0.768', '-0.0663', '0.1724', '-0.0965', '-0.7905', '-1.031', '0.5874', '-0.318', '0.4238', '-0.09875', '0.1934', '-0.1256', '0.696', '-0.3843', '0.7505', '-0.9976', '0.28', '0.4124', '0.418', '0.1416', '-0.0766', '0.5137', '0.295', '-0.5527', '0.9067', '-0.2974', '-0.1758', '0.08', '0.1248', '-0.196', '-0.507', '0.1917', '0.2507', '-0.0785', '0.5674', '0.775', '0.1198', '0.6494', '0.506', '0.03387', '-0.1804', '1.344', '0.1464', '-0.2329', '-0.175', '-0.3137', '0.0849']",,,C565705,,,,
mondo:0012437,cataract 21 multiple types,"['CCA4', 'cataract 21 multiple types with or without microcornea', 'cataract, congenital, cerulean type, 4', 'cataract, pulverulent, juvenile-onset', 'congenital cataract cerulean type 4', 'CTRCT21', 'cataract 21, multiple types', 'cataract 21, multiple types, with or without microcornea', 'MAF early-onset non-syndromic cataract', 'early-onset non-syndromic cataract caused by mutation in MAF']",0110256,610202,98989,,,,,C565703,,,,
mondo:0012438,pontocerebellar hypoplasia type 5,"['olivopontocerebellar hypoplasia, fetal-onset', 'PCH5', 'olivopontocerebellar hypoplasia fetal-onset', 'pontocerebellar hypoplasia, type 5', 'fetal-onset olivopontocerebellar hypoplasia']",0060274,610204,166068,C1857762,"['-0.1504', '0.2034', '-0.369', '0.0611', '0.517', '-0.696', '-0.0853', '0.764', '-0.7437', '0.05457', '-0.2323', '-0.1263', '-0.1896', '-0.361', '0.1581', '-0.3237', '0.1963', '-0.1309', '0.015335', '-0.3892', '-0.3857', '-0.12494', '0.368', '-0.375', '0.2761', '0.3777', '-0.1738', '0.3066', '0.03152', '0.0003593', '0.1857', '0.2805', '0.2769', '0.2168', '0.1222', '-0.2275', '-0.04297', '0.155', '-0.109', '-0.132', '0.1267', '-0.431', '0.224', '0.0689', '-0.4036', '-0.2917', '-0.1973', '0.2673', '0.10895', '-0.1122', '0.2773', '-0.7373', '-0.5293', '0.1437', '0.1885', '-0.4504', '0.3748', '-0.3252', '-0.0175', '0.4421', '-0.1387', '0.1587', '0.515', '0.3306', '0.03717', '-0.056', '0.353', '0.05447', '-0.3223', '0.2362', '0.1742', '0.268', '0.3462', '0.011375', '0.3896', '-0.005253', '0.286', '-0.3337', '-0.479', '0.04935', '0.1812', '0.5664', '-0.2434', '0.1912', '0.01065', '0.05017', '0.1989', '0.5254', '0.6147', '-0.2356', '0.0383', '0.36', '-0.3057', '0.04688', '0.4036', '0.2842', '0.6826', '-0.3572', '0.549', '-0.2032']",,,C537745,,,,
mondo:0012439,Alagille syndrome due to a NOTCH2 point mutation,"['Alagille syndrome 2', 'syndromic bile duct paucity due to a NOTCH2 point mutation', 'ALGS2', 'Alagille syndrome type 2', 'Alagille-Watson syndrome due to a NOTCH2 point mutation', 'Arteriohepatic dysplasia due to a NOTCH2 point mutation']",,610205,261629,C1857761,"['-0.1279', '0.1407', '0.0753', '0.04495', '0.08673', '-0.1741', '0.006603', '0.1434', '-0.1059', '-0.1064', '0.0475', '0.00375', '-0.001222', '0.0095', '0.00893', '-0.05847', '-0.05093', '-0.02554', '-0.01356', '-0.2118', '0.01593', '-0.0082', '0.0857', '-0.045', '0.03174', '-0.007812', '-0.0242', '0.00795', '0.0962', '-0.0183', '0.1354', '0.02068', '0.1343', '0.05002', '-0.0167', '-0.1094', '0.03018', '-0.04712', '0.00849', '-0.2124', '0.0417', '-0.10583', '0.03177', '-0.0728', '-0.05875', '-0.1335', '0.001802', '0.03595', '0.1037', '0.05286', '-0.0468', '-0.03607', '-0.01134', '0.04562', '-0.0775', '-0.03552', '0.1718', '-0.03424', '-0.1523', '0.01776', '0.099', '0.0834', '0.00939', '0.02545', '0.02481', '0.05414', '0.1669', '0.08527', '-0.1348', '0.0853', '-0.1674', '-0.01485', '0.04538', '-0.1175', '0.04156', '0.09814', '0.01735', '0.02806', '-0.10815', '-0.01845', '-0.00687', '0.056', '-0.05878', '0.1375', '-0.01886', '-0.05066', '0.0948', '0.1825', '0.1707', '0.03867', '0.04318', '0.0761', '-0.07764', '-0.04965', '0.2651', '0.065', '0.13', '-0.2135', '0.01076', '0.01797']",,,,,,,
mondo:0012440,"migraine with or without aura, susceptibility to, 10","['migraine with or without aura, susceptibility to, 10', 'migraine with pulsation', 'migraine with or without aura, susceptibility to, type 10', 'Mgr10']",,610208,,,,,,,,,,
mondo:0012441,"migraine with or without aura, susceptibility to, 11","['migraine with or without aura, susceptibility to, 11', 'migraine with or without aura, susceptibility to, type 11', 'Mgr11']",,610209,,,,,,,,,,
mondo:0012442,autosomal recessive nonsyndromic hearing loss 66,"['autosomal recessive nonsyndromic deafness 66', 'DCDC2 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 66', 'deafness, autosomal recessive 66', 'autosomal recessive nonsyndromic deafness caused by mutation in DCDC2', 'DFNB66', 'deafness, autosomal recessive type 66', 'autosomal recessive deafness 66']",0110517,610212,,C1857750,,,,C565701,,,,
mondo:0012443,"aneurysm, intracranial berry, 4","['ANIB4', 'aneurysm, intracranial BERRY, 4']",0080967,610213,,C1857749,,,,C565700,,,,
mondo:0012444,neurodegeneration with brain iron accumulation 2B,"['neurodegeneration with brain iron accumulation 2B', 'neuroaxonal dystrophy, atypical', 'neurodegeneration with brain iron accumulation, Pla2g6-related', 'neurodegeneration with brain iron accumulation, Pla2G6-related', 'early-onset progressive cerebellar ataxia dystonia spasticity and intellectual decline', 'atypical neuroaxonal dystrophy', 'NBIA2B', 'neurodegeneration with brain iron accumulation type 2B', 'NBIA2b', 'neurodegeneration with brain iron accumulation type 2b', 'Karak syndrome']",0110736,610217,,,,,,,,,,
mondo:0012445,autosomal recessive nonsyndromic hearing loss 59,"['deafness, autosomal recessive type 59', 'PJVK autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness caused by mutation in PJVK', 'autosomal recessive nonsyndromic deafness type 59', 'autosomal recessive deafness 59', 'DFNB59', 'deafness, autosomal recessive 59', 'autosomal recessive nonsyndromic deafness 59']",0110511,610220,,C1857744,,,,C565698,,,,
mondo:0012446,seborrhea-like dermatitis with psoriasiform elements,['seborrhea-like dermatitis with psoriasiform elements'],,610227,168606,C1853258,"['-0.0232', '0.4487', '-0.8696', '0.622', '-0.295', '-0.356', '-0.2362', '0.0219', '-0.8223', '0.3936', '0.06573', '0.275', '-0.4414', '-0.312', '-0.7', '0.2242', '-0.08887', '0.02464', '-0.53', '-0.808', '-0.824', '0.0384', '0.383', '-0.311', '0.2708', '-0.05026', '-0.4417', '0.4824', '-0.2422', '-0.5522', '0.257', '-0.001474', '0.3435', '0.0942', '0.5737', '-0.281', '-0.739', '-0.1656', '0.0549', '-0.3696', '0.1885', '-0.292', '-0.7563', '0.494', '0.2263', '-0.137', '-0.1241', '-0.05197', '1.458', '-0.2576', '-0.755', '-0.1364', '0.3308', '0.6772', '-0.304', '0.01189', '0.2932', '0.306', '-0.3982', '-1.018', '-0.331', '0.8164', '0.01921', '0.04584', '0.3298', '0.3328', '0.406', '0.602', '-0.247', '1.184', '-0.1049', '-0.05402', '0.053', '-0.4917', '0.012634', '0.1428', '-0.1063', '0.234', '0.561', '0.213', '0.5225', '-0.1572', '-0.4348', '-0.2385', '0.9243', '-0.2344', '-0.7754', '0.5576', '0.601', '0.9604', '0.3225', '-0.2085', '-0.485', '0.3306', '0.4033', '-0.4885', '-0.2118', '-0.4229', '-0.0678', '-0.4128']",,,C565217,,,,
mondo:0012447,synpolydactyly type 3,"['SD2, Malik type', 'SPD3', 'synpolydactyly, Malik type', 'SD2c', 'synpolydactyly 3', 'SPD, Malik type']",,610234,295199,C1853255,,,,C565216,,,,
mondo:0012448,hereditary spastic paraplegia 33,"['autosomal dominant spastic paraplegia 33', 'ZFYVE27 hereditary spastic paraplegia', 'hereditary spastic paraplegia type 33', 'spastic paraplegia 33, autosomal dominant', 'SPG33', 'hereditary spastic paraplegia caused by mutation in ZFYVE27']",0110784,610244,,C1853251,,,,C565214,,,,
mondo:0012449,spinocerebellar ataxia type 23,"['spinocerebellar ataxia 23', 'spinocerebellar ataxia type 23', 'SCA23']",0050973,610245,101108,C4305146,"['-0.1312', '-0.2128', '-0.1143', '0.08923', '-0.2421', '-0.86', '0.11475', '0.1473', '-0.672', '-1.005', '0.1588', '0.2607', '-0.1318', '0.1512', '0.6753', '-0.406', '-0.2272', '-0.4722', '0.1965', '-0.8994', '-0.2341', '-0.2678', '0.1451', '-0.5205', '0.4985', '-0.3574', '-0.4075', '0.1054', '-0.2656', '-0.8965', '0.306', '0.4556', '-0.47', '-0.1522', '0.4556', '0.1512', '-0.102', '0.1714', '0.3918', '0.508', '0.3943', '0.1755', '-0.495', '0.3923', '0.7524', '-0.6167', '0.0541', '0.4688', '0.2166', '-0.004868', '-0.1906', '-0.01883', '-0.1361', '-0.3848', '0.0629', '-0.743', '0.424', '0.5347', '-0.01768', '0.469', '-0.581', '0.1442', '0.2153', '-0.08905', '-0.393', '0.5596', '0.2737', '0.611', '-0.5483', '0.35', '0.852', '0.4343', '-0.098', '-0.7534', '0.674', '0.3013', '0.275', '0.2532', '0.2083', '0.5327', '-0.4414', '-0.9116', '0.3599', '0.6885', '-0.3435', '-0.6143', '0.317', '0.10425', '0.7676', '0.4578', '0.33', '0.553', '-0.02286', '0.0712', '1.053', '0.9727', '0.3997', '0.525', '-0.2401', '-0.02196']",,,C537201,,,,
mondo:0012450,spinocerebellar ataxia type 28,"['SCA28', 'spinocerebellar ataxia type 28', 'spinocerebellar ataxia 28']",0050977,610246,101109,C4274988,"['-0.25', '-0.3206', '-0.09955', '0.1183', '-0.371', '-0.905', '0.141', '0.225', '-0.716', '-0.9727', '0.1473', '0.222', '-0.08923', '0.2341', '0.667', '-0.2769', '-0.1908', '-0.453', '0.0851', '-0.6626', '-0.1018', '-0.2101', '0.1538', '-0.762', '0.578', '-0.481', '-0.3252', '0.3271', '-0.2942', '-0.9126', '0.059', '0.4211', '-0.376', '-0.1306', '0.3438', '0.06088', '-0.1635', '0.1891', '0.3425', '0.654', '0.3862', '0.1903', '-0.297', '0.4338', '0.5474', '-0.6133', '0.02766', '0.3486', '0.3408', '-0.10406', '-0.0401', '0.2002', '-0.3384', '-0.4053', '0.1617', '-0.7534', '0.4712', '0.5503', '0.04782', '0.5044', '-0.555', '0.1837', '0.2301', '-0.1553', '-0.428', '0.2734', '0.3474', '0.58', '-0.3823', '0.4546', '0.7314', '0.3757', '-0.1924', '-0.6743', '0.8447', '0.2401', '0.0921', '0.204', '0.1841', '0.552', '-0.2346', '-1.037', '0.309', '0.576', '-0.1823', '-0.7656', '0.2944', '-0.03244', '0.562', '0.4417', '0.4272', '0.57', '-0.03574', '-0.0507', '1.012', '1.066', '0.469', '0.3462', '-0.1582', '0.02644']",,,C537205,,,,
mondo:0012451,"esophagitis, eosinophilic, 1","['esophagitis, eosinophilic', 'esophagitis, eosinophilic, 1', 'EOE1']",,610247,,,,,,,,,,
mondo:0012452,autosomal recessive nonsyndromic hearing loss 65,"['autosomal recessive nonsyndromic deafness type 65', 'autosomal recessive nonsyndromic deafness 65', 'DFNB65', 'autosomal recessive deafness 65', 'deafness, autosomal recessive 65']",0110516,610248,,C1853248,,,,C565211,,,,
mondo:0012453,hereditary spastic paraplegia 31,"['hereditary spastic paraplegia caused by mutation in REEP1', 'spastic paraplegia 31', 'hereditary spastic paraplegia type 31', 'spastic paraplegia 31, autosomal dominant', 'autosomal dominant spastic paraplegia type 31', 'autosomal dominant spastic paraplegia 31', 'REEP1 hereditary spastic paraplegia', 'SPG31']",0110782,610250,101011,C1853247,"['-0.0319', '0.253', '-0.2478', '-0.3047', '-0.1901', '-0.6978', '-0.2047', '0.0811', '-0.3777', '-0.4846', '0.01682', '-0.03918', '0.04135', '0.3896', '0.7866', '0.0879', '-0.28', '-0.67', '0.2927', '-0.429', '0.1917', '-0.2181', '0.3203', '0.137', '0.0887', '-0.0911', '0.1', '-0.1866', '-0.139', '-0.2773', '0.322', '0.09436', '0.04813', '0.3496', '0.1752', '-0.3984', '-0.2947', '-0.227', '-0.2559', '-0.1691', '0.06247', '-0.515', '-0.09717', '0.269', '0.0729', '-0.374', '-0.545', '0.4426', '0.02924', '0.1971', '0.05676', '0.205', '-0.443', '-0.227', '0.1598', '-0.6416', '0.7715', '-0.08417', '-0.3054', '0.3618', '-0.0437', '-0.1084', '0.3904', '0.1621', '-0.5425', '0.2191', '0.2678', '0.634', '-0.1669', '0.5225', '-0.068', '-0.0777', '0.1326', '-0.4849', '1.073', '0.4116', '-0.2395', '0.02158', '-0.2179', '-0.1836', '-0.015236', '-0.3145', '0.863', '0.98', '-0.004536', '0.1633', '-0.06223', '0.08453', '0.1365', '-0.1698', '0.5312', '0.03033', '0.101', '0.2883', '0.7075', '0.407', '0.5293', '0.0916', '-0.3237', '0.03848']",,,C565210,,,,
mondo:0012454,"alcohol sensitivity, acute","['Hangover, susceptibility to', 'acute alcohol sensitivity', 'alcohol intolerance', 'alcohol sensitivity, acute']",,610251,,,,,,,,,,
mondo:0012455,Kleefstra syndrome,"['9Q- syndrome', 'Kleefstra syndrome', '9q34.3 microdeletion syndrome', '9Q subtelomeric deletion syndrome', 'chromosome 9q deletion syndrome', 'chromosome 9Q34.3 deletion syndrome', '9q34 deletion syndrome', '9q-syndrome']",0080597,,261494,,"['0.3616', '0.0373', '0.37', '-0.264', '-0.03152', '-0.2028', '0.6304', '1.201', '-0.4465', '-0.265', '-0.324', '-0.4688', '0.1832', '0.208', '0.01145', '-0.0429', '-0.3118', '0.1125', '-0.4727', '-0.597', '0.3584', '0.02255', '0.1277', '-0.288', '0.1307', '-0.4731', '0.06094', '0.1018', '0.7856', '-0.2455', '0.3022', '0.03345', '0.539', '0.3164', '0.0727', '-0.3086', '-0.3074', '0.03683', '-0.01411', '-0.3564', '0.7036', '-0.07776', '-0.2345', '0.0618', '0.09796', '-0.3167', '-0.2085', '0.2812', '-0.5254', '0.1362', '-0.626', '0.6953', '-0.4028', '-0.2825', '-0.4065', '0.2224', '-0.003725', '-0.255', '0.09485', '0.0003629', '0.05066', '0.1746', '0.2081', '-0.06934', '0.589', '0.0525', '0.1785', '0.08624', '-0.1727', '0.3425', '-0.1783', '-0.06354', '-0.4165', '-0.01888', '0.1698', '-0.4133', '0.0651', '-0.314', '-0.5825', '-0.407', '0.0437', '-0.003456', '-0.3088', '0.5693', '0.0752', '0.3694', '-0.03903', '-0.353', '0.4539', '0.3457', '0.07385', '0.1384', '-0.2935', '0.06696', '0.4514', '-0.3198', '0.2322', '-0.3914', '0.367', '0.3184']",,,,,,,
mondo:0012456,congenital primary aphakia,"['aphakia, congenital primary', 'ASGD2', 'CPA', 'congenital aphakia', 'anterior segment dysgenesis 2, multiple subtypes', 'congenital absence of lens', 'anterior segment dysgenesis 2']",11367,610256,83461,,"['-0.2202', '-0.1907', '-0.0441', '0.06195', '0.05148', '-0.0003347', '0.4263', '0.3835', '-0.486', '-0.46', '-0.10834', '-0.681', '0.3708', '0.565', '-0.2866', '-0.09326', '-0.0877', '0.1076', '-0.1088', '-1.346', '-0.0143', '0.3113', '0.956', '-0.599', '0.0857', '-0.2441', '-0.37', '0.6978', '0.1163', '-0.01326', '0.1902', '-0.21', '-0.00519', '0.2522', '-0.421', '0.3508', '0.5117', '-0.666', '-0.07214', '-0.6523', '0.589', '-0.1494', '0.512', '0.1097', '-0.0839', '-0.2817', '0.2976', '-0.7686', '0.2917', '-0.02686', '-0.05295', '-0.504', '0.6846', '-0.5913', '0.1516', '-0.5664', '0.6255', '0.214', '-0.1903', '-0.263', '-0.1683', '-0.2168', '0.2844', '0.363', '0.04477', '0.1707', '0.58', '0.8306', '-0.47', '-0.287', '-0.1326', '0.448', '-0.4253', '0.2015', '0.162', '-0.5483', '0.4424', '-0.393', '-0.2189', '0.3955', '0.2856', '0.8247', '-0.5303', '0.911', '-0.3052', '-0.4365', '0.7026', '0.2129', '0.04242', '0.382', '0.038', '0.2289', '-0.3284', '0.2905', '0.6636', '-0.657', '0.627', '-0.3203', '-0.0962', '-0.361']",C35172,,C537786,743.35,Q12.3,10002947,
mondo:0012457,"pyloric stenosis, infantile hypertrophic, 2","['IHPS2', 'pyloric stenosis, infantile hypertrophic, 2']",,610260,,C1853228,,,,C565208,,,,
mondo:0012458,"hypertension, essential, susceptibility to, 5","['Hyt5', 'hypertension, essential, susceptibility to, 5', 'hypertension, essential, body Mass-related', 'hypertension, essential, susceptibility to, type 5']",,610261,,,,,,,,,,
mondo:0012459,"hypertension, essential, susceptibility to, 6","['hypertension, essential, susceptibility to, 6', 'Hyt6', 'hypertension, essential, kidney function-related', 'hypertension, essential, susceptibility to, type 6']",,610262,,,,,,,,,,
mondo:0012460,autosomal recessive nonsyndromic hearing loss 67,"['LHFPL5 autosomal recessive nonsyndromic deafness', 'DFNB67', 'deafness, autosomal recessive 67', 'autosomal recessive nonsyndromic deafness caused by mutation in LHFPL5', 'autosomal recessive nonsyndromic deafness type 67', 'autosomal recessive nonsyndromic deafness 67', 'autosomal recessive deafness 67', 'deafness, autosomal recessive type 67']",0110518,610265,,C1853223,,,,C565207,,,,
mondo:0012462,autosomal recessive frontotemporal pachygyria,"['pachygyria, frontotemporal']",,610279,329329,C1853215,,,,C538092,,,,
mondo:0012463,retinitis pigmentosa 35,"['retinitis pigmentosa 35', 'SEMA4A retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in SEMA4A', 'RP 35', 'retinitis pigmentosa type 35', 'RP35']",0110357,610282,,C1853214,,,,C565206,,H35.5,,
mondo:0012464,cone-rod dystrophy 10,"['SEMA4A cone-rod dystrophy', 'CORD10', 'cone-rod dystrophy 10', 'cone-rod dystrophy caused by mutation in SEMA4A', 'cone-rod dystrophy type 10']",0111017,610283,,C1846529,,,,C564597,,,,
mondo:0012465,hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency,"['glycosylphosphatidylinositol deficiency', 'congenital disorder of glycosylation due to PIGM deficiency', 'PIGM-CDG', 'glycosylphosphatidylinositol biosynthesis defect 1', 'GPID', 'GPI deficiency']",,610293,83639,C4510605,"['-0.623', '-0.00274', '0.1835', '0.0064', '0.1456', '-0.365', '0.2527', '-0.059', '0.245', '-0.349', '-0.277', '-0.4983', '-0.1135', '-0.289', '0.1648', '-0.0653', '-0.1908', '-0.4395', '-0.12415', '-0.5576', '-0.0878', '-0.0585', '0.3748', '-0.4524', '0.2617', '0.01807', '0.464', '0.635', '0.08575', '0.3506', '0.4207', '0.1448', '0.3633', '0.1603', '-0.4048', '-0.2773', '0.02309', '-0.07007', '-0.1633', '-0.5547', '0.4888', '-0.3071', '0.3765', '0.2477', '-0.2056', '-0.1263', '0.2698', '0.03845', '-0.05548', '-0.4885', '0.2344', '-0.0596', '0.2094', '0.3936', '-0.2256', '-0.0329', '0.698', '0.4385', '-0.699', '0.6562', '-0.3745', '0.03613', '0.03363', '-0.3218', '-0.2432', '-0.1814', '-0.1067', '0.3699', '-0.3677', '0.4058', '-0.4375', '0.531', '0.01715', '-0.0849', '0.0584', '0.4158', '0.4954', '-0.332', '-0.01316', '0.2498', '-0.1967', '0.2913', '0.02412', '0.382', '0.5503', '-0.04074', '0.2932', '0.5205', '0.1788', '-0.536', '0.1642', '0.616', '-0.5205', '-0.4346', '0.774', '0.4805', '0.361', '-0.4023', '0.2397', '-0.2666']",,,,,,,
mondo:0012466,"Parkinson disease 13, autosomal dominant, susceptibility to","['Parkinson disease 13', 'PARK13', 'young-onset Parkinson disease caused by mutation in HTRA2', 'HTRA2 young-onset Parkinson disease', 'Parkinson disease 13, autosomal dominant, susceptibility to', 'susceptibility to autosomal dominant Parkinson disease 13']",,610297,,,,,,C565204,,,,
mondo:0012467,cold-induced sweating syndrome 2,"['Crisponi/cold-induced sweating syndrome 2', 'cold-induced sweating syndrome type 2', 'CISS2', 'CRISPONI/cold-induced sweating syndrome 2', 'cold-induced sweating syndrome 2', 'CLCF1 cold-induced sweating syndrome', 'cold-induced sweating syndrome caused by mutation in CLCF1']",0080330,610313,,C1853198,,,,C564791,,,,
mondo:0012468,"rhizomelic dysplasia, scoliosis, and retinitis pigmentosa","['rhizomelic dysplasia, scoliosis, and retinitis pigmentosa']",,610319,,C1853197,,,,C537610,,,,
mondo:0012469,myopia 14,"['MYP14', 'myopia 14']",,610320,,C1853196,,,,C565202,,,,
mondo:0012470,"prostate cancer, hereditary, 7","['HPC7', 'prostate cancer, hereditary, 7', 'prostate cancer aggressiveness']",,610321,,C1853195,,,,C565201,,,,
mondo:0012471,Aicardi-Goutieres syndrome 3,"['RNASEH2C Aicardi-Goutieres syndrome', 'Aicardi-Goutieres syndrome type 3', 'Aicardi-Goutieres syndrome 3', 'RNASEH2C -related Aicardi-Goutieres syndrome', 'Aicardi-Goutieres syndrome caused by mutation in RNASEH2C', 'AGS3']",,610329,,C1835916,,,,C563683,,,,
mondo:0012472,Aicardi-Goutieres syndrome 4,"['Aicardi-Goutieres syndrome type 4', 'Aicardi-Goutieres syndrome 4', 'RNASEH2A Aicardi-Goutieres syndrome', 'RNASEH2A-related Aicardi-Goutieres syndrome', 'Aicardi-Goutieres syndrome caused by mutation in RNASEH2A', 'AGS4']",,610333,,C1835912,,,,C563681,,,,
mondo:0012473,"right pulmonary artery, anomalous origin of, familial","['familial ARPA', 'familial anomalous origin of right pulmonary artery', 'ARPA familial', 'Arpa, familial', 'right pulmonary artery, anomalous origin of, familial', 'anomalous origin of right pulmonary artery familial', 'right pulmonary artery, anomalous origin of, with ventricular septal defect, patent Foramen ovale, and patent ductus arteriosus']",,610338,,C1835910,,,,C535681,,,,
mondo:0012474,autosomal dominant nocturnal frontal lobe epilepsy 4,"['autosomal dominant nocturnal frontal lobe epilepsy type 4', 'epilepsy, familial, with nocturnal wandering and Ictal fear', 'epilepsy, nocturnal frontal lobe, type 4', 'seizures, benign familial infantile, 6', 'nocturnal frontal lobe epilepsy 4', 'CHRNA2 autosomal dominant nocturnal frontal lobe epilepsy', 'epilepsy, nocturnal frontal lobe, 4', 'convulsions, benign familial infantile, 6', 'autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA2', 'ENFL4']",0081119,610353,,C1835905,,,,C563679,,,,
mondo:0012475,cone dystrophy with supernormal rod response,"['cone dystrophy with supernormal rod ERG', 'retinal cone dystrophy type 3B', 'cone dystrophy with night blindness and supernormal rod responses KCNV2 related', 'retinal cone dystrophy 3B', 'cone dystrophy with supernormal Rod responses', 'cone dystrophy with supernormal scotopic electroretinogram', 'cone dystrophy with night blindness and supernormal Rod responses, Kcnv2-related', 'cone dystrophy with supernormal rod electroretinogram', 'RCD3B']",0081022,610356,209932,C4304714,"['-0.6826', '0.10834', '-0.1431', '0.0854', '0.0827', '-0.5107', '-0.1378', '0.2866', '-0.1581', '-0.31', '-0.0937', '0.1758', '-0.331', '-0.00838', '-0.1776', '-0.3147', '0.3374', '-0.1335', '-0.1009', '-0.7847', '-0.2556', '-0.332', '-0.0693', '0.2815', '-0.235', '0.0591', '-0.1958', '-0.03638', '-0.419', '0.2067', '0.6353', '0.301', '0.00836', '0.277', '-0.1895', '0.3962', '-0.004555', '0.08185', '-0.1641', '-0.11664', '0.2207', '0.0439', '0.1705', '0.11664', '-0.3467', '0.3591', '0.02405', '-0.1002', '0.2086', '0.605', '0.5034', '0.3123', '-0.0532', '-0.1738', '0.0883', '-0.1624', '0.595', '-0.2026', '-0.3848', '0.1658', '0.1233', '0.1375', '0.311', '0.368', '-0.0921', '0.04553', '0.685', '0.605', '-0.1035', '0.5557', '-0.38', '0.004852', '0.281', '-0.1707', '0.566', '-0.01027', '0.1951', '-0.1462', '0.03915', '-0.1566', '-0.003672', '-0.289', '0.1711', '0.4536', '-0.1171', '-0.2673', '-0.1652', '-0.0937', '0.4065', '0.1477', '0.234', '0.335', '0.1984', '0.339', '0.1342', '0.2974', '0.05435', '-0.3523', '-0.014244', '0.04858']",,,C563678,,,,
mondo:0012476,hereditary spastic paraplegia 30,"['spastic paraplegia 30, autosomal recessive', 'hereditary spastic paraplegia caused by mutation in KIF1A', 'hereditary spastic paraplegia type 30', 'autosomal spastic paraplegia type 30', 'KIF1A hereditary spastic paraplegia', 'SPG30', 'autosomal recessive spastic paraplegia 30', 'spastic paraplegia 30, autosomal dominant']",0110781,610357,101010,C1835896,"['-0.527', '0.553', '-0.3586', '-0.1995', '-0.183', '-1.004', '-0.3257', '0.2808', '-0.7944', '-0.4248', '-0.3696', '0.2087', '-0.04163', '0.0944', '0.4016', '-0.364', '0.546', '-0.7188', '0.7305', '-0.87', '0.1849', '0.0907', '-0.05634', '0.021', '0.504', '0.06082', '-0.183', '-0.03009', '0.07086', '-0.2108', '0.098', '0.2239', '0.1932', '0.1863', '0.05426', '-0.5215', '-0.8696', '-0.503', '-0.7163', '-0.1593', '0.2544', '-0.613', '0.2502', '0.4429', '0.1443', '-0.1986', '-0.7686', '0.2107', '-0.11816', '0.139', '-0.01133', '0.5967', '-0.3228', '-0.6943', '-0.04132', '-0.588', '0.534', '-0.1465', '-0.3054', '0.093', '0.1329', '0.27', '0.319', '0.2489', '-0.3765', '0.4775', '0.7026', '0.6685', '-0.1279', '0.1342', '0.04517', '0.3596', '0.7534', '-0.6406', '0.7656', '0.1273', '0.2499', '0.04324', '0.3628', '0.0703', '-0.3948', '-0.2295', '0.513', '0.7007', '-0.1313', '0.09406', '-0.3108', '0.514', '0.2688', '0.07275', '0.242', '0.535', '0.793', '0.1443', '0.7725', '0.618', '0.3684', '0.0901', '-0.2615', '0.65']",,,C563677,,,,
mondo:0012477,retinitis pigmentosa 33,"['SNRNP200 retinitis pigmentosa', 'retinitis pigmentosa 33', 'retinitis pigmentosa caused by mutation in SNRNP200', 'RP 33', 'retinitis pigmentosa type 33', 'RP33']",0110366,610359,,C1835895,,,,C563676,,H35.5,,
mondo:0012478,orofacial cleft 9,"['orofacial cleft 9', 'cleft lip with or without cleft palate, nonsyndromic, 9', 'OFC9']",0080402,610361,,C1835894,,,,C563675,,,,
mondo:0012479,congenital malabsorptive diarrhea 4,"['congenital diarrhea caused by mutation in NEUROG3', 'congenital malabsorptive diarrhea due to paucity of enteroendocrine cells', 'congenital diarrhoea caused by mutation in NEUROG3', 'NEUROG3 congenital diarrhea', 'NEUROG3 congenital diarrhoea', 'congenital malabsorptive diarrhoea type 4', 'enteric anendocrinosis', 'congenital malabsorptive diarrhoea due to paucity of enteroendocrine cells', 'DIAR4', 'diarrhea 4, malabsorptive, congenital', 'congenital malabsorptive diarrhea type 4', 'diarrhoea 4, malabsorptive, congenital']",0060779,610370,83620,C1835888,"['0.1843', '0.04086', '0.541', '0.481', '-0.5444', '-0.667', '-0.9546', '0.4197', '0.1058', '-0.1332', '0.709', '0.4734', '0.299', '0.654', '-0.9897', '-0.10315', '-0.3008', '-0.02078', '-0.5996', '-0.6025', '-0.01068', '-0.2876', '-0.2998', '0.2064', '0.02046', '-0.4297', '-0.756', '0.6377', '0.4392', '-1.256', '-0.2247', '-0.0912', '-0.03442', '0.2686', '0.8193', '0.69', '-0.2974', '0.1926', '0.01398', '0.1283', '-0.6357', '-0.3923', '-0.4004', '-0.591', '0.3623', '0.11536', '0.10504', '0.246', '-0.07623', '0.7944', '-0.7603', '-0.284', '0.144', '-0.4585', '0.2302', '-0.1241', '-0.2375', '-0.2566', '-0.5947', '0.05484', '0.521', '0.8315', '0.3752', '-0.5977', '0.2399', '-0.3162', '0.3083', '-0.1543', '0.1759', '0.9844', '-0.457', '0.4077', '0.2332', '-0.5176', '0.932', '0.2544', '-0.775', '0.3599', '0.05185', '0.92', '-0.10126', '-0.8926', '-0.1409', '0.12463', '0.1934', '0.3052', '0.4397', '0.2864', '0.2113', '-0.4504', '0.012825', '-0.1539', '-0.2834', '-0.4946', '0.4324', '0.4912', '0.2091', '-1.544', '0.006653', '0.0721']",,,C563673,,,,
mondo:0012480,"diabetes mellitus, transient neonatal, 2","['ABCC8 transient neonatal diabetes mellitus (disease)', 'diabetes mellitus, transient neonatal, 2', 'Tndm2', 'diabetes mellitus, transient neonatal, type 2', 'diabetes mellitus, transient neonatal 2']",,610374,,C1835887,,,,C563672,,,,
mondo:0012481,mevalonic aciduria,"['HIDS', 'hyperimmunoglobulin D with periodic fever syndrome', 'Mevalonicaciduria', 'mevalonic aciduria', 'MEVA', 'MVA', 'MKD', 'complete mevalonate kinase deficiency']",0050452,610377,29,C1959626,"['-0.857', '-0.1488', '-0.9243', '-0.4636', '0.1506', '-0.5356', '-0.0228', '0.841', '-0.7007', '-0.05347', '0.1663', '-0.3281', '0.04227', '-0.1205', '-0.3665', '0.0664', '0.2189', '-0.2087', '0.2244', '-0.905', '0.3765', '-0.5786', '-0.1741', '-0.664', '0.06506', '0.2104', '-0.4902', '-0.3618', '-0.1294', '-0.07074', '0.0572', '-0.1519', '0.523', '0.1096', '0.1753', '0.445', '0.1217', '-0.7896', '-0.5195', '0.0919', '-0.2155', '-0.822', '0.2678', '0.349', '-0.2072', '0.1909', '-0.3628', '-0.004543', '-0.0807', '0.4075', '0.0749', '-0.083', '0.207', '0.843', '-0.2455', '-0.1094', '-0.4683', '-0.808', '0.2417', '0.6167', '-0.5244', '-0.1323', '-0.3865', '0.197', '0.427', '-0.5913', '0.62', '0.7593', '-0.1483', '0.9272', '-0.05963', '-0.2964', '-0.2164', '0.4185', '-0.2142', '0.607', '0.5903', '-0.787', '0.3154', '0.388', '0.438', '-0.3406', '-0.3745', '0.2505', '0.05786', '0.2041', '-0.09', '0.3667', '1.001', '0.394', '1.007', '-0.1515', '0.1095', '-0.009445', '0.381', '0.6885', '0.3135', '-0.1058', '0.04745', '0.05212']",C84890,,,,,10072219,
mondo:0012482,"West Nile virus, susceptibility to","['West Nile virus, susceptibility to', 'WNV, susceptibility to']",,610379,,,,,,,,,,
mondo:0012483,cone-rod dystrophy 11,"['CORD11', 'RAX2 cone-rod dystrophy', 'cone-rod dystrophy type 11', 'cone-rod dystrophy caused by mutation in RAX2', 'cone-rod dystrophy 11']",0111018,610381,,C1835865,,,,C563671,,,,
mondo:0012484,"prosopagnosia, hereditary","['prosopagnosia, congenital', 'prosopagnosia, hereditary', 'hereditary prosopagnosia', 'congenital prosopagnosia', 'hereditary prosopagnosia (disease)', 'developmental prosopagnosia', 'prosopagnosia, developmental', 'face blindness']",,610382,,C2931455,,,,C537242,,,,
mondo:0012485,autosomal recessive nonsyndromic hearing loss 68,"['autosomal recessive nonsyndromic deafness caused by mutation in S1PR2', 'autosomal recessive deafness 68', 'DFNB68', 'autosomal recessive nonsyndromic deafness 68', 'S1PR2 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 68', 'deafness, autosomal recessive 68']",0110519,610419,,C1835854,,,,C563669,,,,
mondo:0012486,"preauricular tag, isolated, autosomal dominant, 1","['preauricular tag, isolated, autosomal dominant, 1', 'preauricular Tag, isolated, autosomal dominant, type 1']",,610420,,C1968893,,,,C566904,,,,
mondo:0012487,alopecia-intellectual disability syndrome 2,"['AMR syndrome 2', 'alopecia with mild to moderate intellectual deficit', 'alopecia intellectual disability syndrome 2', 'alopecia-mental retardation syndrome 2', 'APMR2', 'alopecia-intellectual disability syndrome 2']",0080629,610422,,C1835852,,,,C563668,,,,
mondo:0012488,"hepatitis B virus, susceptibility to","['HBV, susceptibility to', 'HBV, resistance to', 'hepatitis b virus, susceptibility to', 'Hepatitis B Virus, resistance to', 'hepatitis B virus infection, susceptibility to']",,610424,,C3552304,,,,,,,,
mondo:0012489,cataract 23,"['early-onset non-syndromic cataract caused by mutation in CRYBA4', 'cataract type 23', 'CTRCT23', 'lamellar cataract 23', 'cataract 23, multiple types', 'CRYBA4 early-onset non-syndromic cataract', 'cataract 23, multiple types, with or without microcornea', 'cataract 23, lamellar', 'cataract 23']",0110271,610425,98995,C3808012,,,,,,,,
mondo:0012490,"cone-rod synaptic disorder, congenital nonprogressive","['night blindness, congenital stationary, type 2B, formerly', 'night blindness, congenital stationary, type 2B', 'night blindness, congenital stationary, incomplete, autosomal recessive', 'night blindness, congenital stationary, incomplete, autosomal recessive, formerly', 'cone-rod synaptic disorder, congenital nonprogressive', 'CRSD']",,610427,,C1864877,,,,,,,,
mondo:0012491,"macroglobulinemia, Waldenstrom, 2","['macroglobulinemia, WALDENSTROM, susceptibility to, 2', 'WM2']",,610430,,,,,,,,,,
mondo:0012492,"restless legs syndrome, susceptibility to, 3","['restless legs syndrome 3', 'RLS3', 'restless legs syndrome, susceptibility to, 3']",,610438,,,,,,,,,,
mondo:0012493,"restless legs syndrome, susceptibility to, 4","['restless legs syndrome 4', 'restless legs syndrome, susceptibility to, 4', 'RLS 4', 'RLS4']",,610439,,,,,,,,,,
mondo:0012494,testicular microlithiasis,"['testicular microlithiasis (disease)', 'testicular microlithiasis']",,610441,,C1864873,,,,C566478,,,,0012215
mondo:0012495,"spondyloepimetaphyseal dysplasia, Genevieve type","['spondyloepimetaphyseal dysplasia, Genevieve type', 'SEMDG', 'spondyloepimetaphyseal dysplasia, Geneviève type', 'SEMD, Geneviève type', 'SEMD, Genevieve type', 'SEMD Genevieve type', 'spondyloepimetaphyseal dysplasia Genevieve type', 'Nans deficiency', 'spondyloepimetaphyseal dysplasia, Camera-Genevieve type']",0080576,610442,168454,C1864872,"['-0.3801', '-0.0989', '0.5317', '-0.3328', '0.44', '-0.3015', '-0.1304', '0.717', '-0.91', '-0.1394', '-0.035', '0.04086', '0.5225', '-0.4038', '-0.06976', '0.05472', '0.419', '-0.192', '-0.5474', '-0.613', '0.2708', '0.1786', '0.4607', '-0.132', '0.4858', '-0.10504', '0.01502', '-0.2106', '0.4146', '0.02766', '0.1422', '-0.05536', '0.2708', '0.1724', '0.4685', '-0.3733', '-0.3796', '-0.4807', '0.053', '-0.911', '0.2517', '-0.48', '-0.1613', '-0.00821', '-0.3562', '-0.4915', '0.10834', '0.5103', '0.10706', '-0.197', '-0.0921', '0.1868', '-0.02017', '0.397', '-0.3762', '-0.4133', '-0.10223', '-0.2048', '0.1278', '0.1437', '0.059', '0.3516', '-0.4841', '-0.1528', '0.1344', '0.1298', '-0.0342', '0.4136', '-0.198', '0.2693', '-0.381', '0.01855', '0.1249', '-0.2218', '-0.6533', '0.2043', '0.3623', '-0.03677', '-0.2893', '0.288', '-0.04428', '0.1293', '-0.261', '0.465', '-0.0365', '0.165', '-0.1554', '0.53', '0.595', '0.2788', '-0.263', '0.262', '0.3247', '0.0926', '0.856', '0.2842', '0.4866', '-0.4917', '0.684', '0.2827']",,,C535785,,,,
mondo:0012496,Koolen-de Vries syndrome,"['17q21.31 deletion syndrome', 'chromosome 17Q21.31 deletion syndrome', 'KANSL1-related intellectual disability syndrome', 'microdeletion 17Q21.31 syndrome', 'Koolen-De Vries syndrome', 'chromosome 17q21.31 deletion syndrome', 'KDVS', 'KdVS', 'chromosome 17q21.31 microdeletion syndrome', 'Koolen-DE Vries syndrome', 'microdeletion 17q21.31 syndrome']",,610443,96169,CN776874,"['-0.05212', '0.02878', '0.0956', '-0.3406', '0.013275', '-0.4944', '0.219', '1.032', '-0.904', '-0.6436', '0.03806', '-0.03677', '0.5103', '0.2903', '-0.1442', '0.3914', '-0.2307', '-0.1713', '-0.2001', '-0.819', '-0.04468', '0.5083', '0.5913', '-0.2379', '0.3245', '-0.3137', '-0.1792', '0.2827', '0.4468', '-0.3665', '0.3936', '-0.2354', '0.5312', '0.2096', '-0.2009', '0.0414', '0.2462', '-0.3', '-0.3008', '0.03796', '0.4229', '0.1355', '0.4858', '0.2336', '0.1416', '-0.1619', '0.1692', '0.4072', '-0.3987', '-0.3918', '-0.7812', '0.1196', '-0.4612', '0.5303', '-0.2952', '-0.088', '0.3872', '0.4512', '0.1146', '-0.01312', '0.00315', '-0.02711', '0.1217', '0.2428', '0.3408', '-0.4531', '0.1843', '0.4937', '-0.3184', '0.0269', '-0.06036', '0.1694', '-0.811', '-0.2042', '-0.05316', '0.1877', '0.1418', '-0.4902', '-0.95', '0.4294', '0.2126', '0.0857', '0.08264', '0.5044', '-0.0971', '0.1273', '-0.4426', '-0.1909', '0.3284', '0.3025', '-0.11816', '0.2927', '-0.4702', '0.3848', '0.1387', '-0.3442', '0.9834', '-0.2546', '0.1516', '0.518']",,,,,,,
mondo:0012497,congenital stationary night blindness autosomal dominant 3,"['Nougaret type congenital stationary night blindness', 'night blindness, congenital stationary, autosomal dominant 3', 'congenital stationary night blindness autosomal dominant type 3', 'CSNBAD3', 'night blindness, congenital stationary, autosomal dominant type 3', 'night blindness, congenital stationary, Nougaret type']",0110715,610444,,C1864870,,,,C566475,,,,
mondo:0012498,congenital stationary night blindness autosomal dominant 1,"['RHO congenital stationary night blindness', 'night blindness, congenital stationary, autosomal dominant 1', 'CSNBAD1', 'night blindness, congenital stationary, autosomal dominant type 1', 'night blindness, congenital stationary, rhodopsin-related', 'congenital stationary night blindness autosomal dominant type 1', 'congenital stationary night blindness caused by mutation in RHO', 'rhodopsin-related congenital stationary night blindness']",0110862,610445,,C1864869,,,,C566474,,,,
mondo:0012499,"Buruli ulcer, susceptibility to","['Buruli ulcer, susceptibility to', 'BUD', 'Mycobacterium ulcerans, susceptibility to']",,610446,,,,,,,,,,
mondo:0012500,chilblain lupus 1,"['chilblain lupus', 'chilblain lupus caused by mutation in TREX1', 'chilblain lupus 1', 'TREX1 chilblain lupus', 'chilblain lupus type 1', 'CHBL1']",,610448,,,,,,,,,,
mondo:0012502,normophosphatemic familial tumoral calcinosis,"['familial normophosphatemic tumoral calcinosis', 'tumoral calcinosis, normophosphatemic, familial', 'calcinosis, tumoral, with Normophosphatemia', 'tumoral calcinosis, familial, normophosphatemic', 'NFTC']",0080170,610455,306658,,"['-0.05084', '0.1166', '0.01429', '-0.01323', '0.02763', '-0.08936', '-0.04773', '0.069', '-0.05307', '0.05695', '-0.0523', '0.02306', '-0.007668', '-0.0217', '-0.03833', '-0.02936', '-0.0228', '-0.01926', '-0.009865', '-0.133', '-0.02536', '-0.04108', '0.0992', '-0.07184', '0.0423', '0.0326', '-0.01098', '-0.04437', '-0.03555', '-0.1102', '0.0734', '-0.04593', '0.09143', '0.035', '0.01692', '-0.03806', '-0.01074', '-0.0374', '-0.01252', '-0.1239', '0.02902', '-0.1652', '0.0709', '-0.087', '0.02773', '-0.09485', '-0.02489', '0.0724', '-0.03485', '0.02037', '0.0214', '-0.02852', '-0.001404', '0.05362', '-0.11017', '-0.08014', '0.09845', '-0.05872', '-0.1366', '0.05634', '0.0701', '0.05597', '-0.0671', '0.0008965', '0.013084', '-0.01476', '0.09186', '0.0838', '-0.0989', '0.0979', '-0.0769', '0.0244', '0.05893', '-0.05844', '0.04834', '0.0894', '-0.05374', '0.01064', '-0.0581', '-0.0552', '-0.00885', '0.03406', '-0.0005755', '0.0784', '-0.013824', '-0.01534', '0.02463', '0.07587', '0.0682', '-0.01261', '0.05737', '0.0875', '0.03223', '-0.00992', '0.2173', '0.0166', '0.1248', '-0.1792', '-0.05997', '-0.01976']",,,C566473,,,,
mondo:0012503,thiopurine S-methyltransferase deficiency,"['Thiopurines, poor metabolism of', '6-mercaptopurine sensitivity', 'inborn error of thiopurine S-methyltransferase activity', 'Thiopurines, poor metabolism of, 1', 'TPMT deficiency', 'poor metabolism of thiopurines-1', 'thiopurine S-methyltransferase deficiency', 'THPM1', 'thiopurine methyltransferase deficiency', 'rare inborn error of thiopurine S-methyltransferase activity', 'thiopurines, poor metabolism of, 1', 'thiopurine S methyltranferase deficiency']",0080172,610460,3315,,"['-0.3594', '0.1613', '-0.002146', '-0.001409', '0.1027', '-0.1838', '-0.03442', '0.0968', '-0.12115', '0.03058', '-0.0569', '-0.05493', '0.082', '-0.10223', '-0.05945', '-0.05118', '-0.0649', '-0.0829', '-0.2191', '-0.341', '0.1315', '-0.0842', '0.1251', '-0.06445', '0.0724', '-0.11127', '0.03552', '-0.0712', '-0.08075', '-0.05157', '0.2197', '0.1404', '0.1807', '0.147', '0.04034', '-0.1592', '0.03735', '-0.0832', '0.02762', '-0.2734', '0.1069', '-0.2115', '0.07324', '-0.005424', '-0.08594', '-0.2307', '0.1168', '0.03882', '0.1163', '0.05423', '-0.01554', '-0.0651', '0.01768', '0.145', '-0.0997', '-0.1514', '0.2976', '-0.086', '-0.2766', '0.05542', '0.05652', '0.09424', '0.1602', '-0.027', '0.09656', '0.1237', '0.1649', '-0.01142', '-0.1788', '0.1115', '-0.2244', '0.01246', '0.02478', '-0.1229', '0.08923', '0.0958', '-0.01521', '0.03656', '-0.13', '-0.1747', '0.1515', '0.1477', '-0.0708', '0.09247', '0.03647', '0.01819', '0.1284', '0.1571', '0.1764', '0.00415', '0.0416', '0.1521', '-0.015366', '-0.05127', '0.3052', '0.2482', '0.10767', '-0.371', '-0.0454', '-0.01259']",C4389,,C536512,,,,
mondo:0012504,camptodactyly-tall stature-scoliosis-hearing loss syndrome,"['CATSHLS', 'CATSHL syndrome', 'camptodactyly, tall stature, and hearing loss syndrome']",0111160,610474,85164,C1864852,"['0.4788', '0.2155', '0.4592', '0.4368', '-0.645', '-0.11444', '1.124', '0.92', '-0.1345', '-0.898', '0.3909', '0.1748', '-0.3782', '0.2803', '-0.2764', '-0.5654', '-0.549', '0.0899', '-0.6123', '-0.1888', '0.144', '0.3564', '-0.711', '0.3677', '1.095', '0.3174', '-1.2', '0.1197', '-0.668', '-0.08795', '0.336', '-0.3047', '0.2822', '-0.3599', '-0.272', '-0.5605', '-0.3362', '-0.6797', '0.0727', '-0.7056', '0.1525', '0.04614', '-0.01607', '-0.2615', '0.0918', '-0.794', '0.1683', '0.2795', '0.1148', '-0.2349', '-0.191', '-0.5713', '-0.165', '0.2346', '0.549', '0.4465', '0.1946', '0.2698', '-0.3096', '0.6123', '-0.2578', '0.997', '-0.441', '0.10645', '-0.4614', '0.2361', '-0.7397', '1.016', '-0.5796', '-0.564', '-0.0404', '0.8594', '1.013', '-1.093', '0.348', '-0.07776', '0.8086', '0.661', '0.2612', '-0.0422', '0.2026', '-0.6885', '-0.5605', '0.686', '-0.013245', '-0.3694', '0.02122', '1.491', '0.0987', '0.698', '0.1548', '0.416', '-0.1414', '0.4512', '0.729', '-0.0611', '-0.1448', '-1.358', '-0.1661', '-0.05753']",,,C537975,,,,
mondo:0012505,"pigmented nodular adrenocortical disease, primary, 2","['pigmented nodular adrenocortical disease, primary, type 2', 'PDE11A primary pigmented nodular adrenocortical disease', 'pigmented nodular adrenocortical disease, primary, 2', 'Cushing syndrome, adrenal, due to PPNAD2', 'pigmented micronodular adrenocortical disease, primary, 2', 'PPNAD2', 'primary pigmented nodular adrenocortical disease caused by mutation in PDE11A']",,610475,,C1864851,,,,C566472,,,,
mondo:0012506,arrhythmogenic right ventricular dysplasia 11,"['arrhythmogenic right ventricular dysplasia, familial, 11, and mild palmoplantar keratoderma with or without wooly hair', 'ARVD11', 'arrhythmogenic right ventricular dysplasia, familial, 11, and mild palmoplantar keratoderma with or without woolly hair', 'arrhythmogenic right ventricular dysplasia type 11', 'arrhythmogenic right ventricular dysplasia, familial, 11', 'DSC2 familial isolated arrhythmogenic right ventricular dysplasia', 'ARVC11', 'arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and woolly hair', 'arrhythmogenic right ventricular cardiomyopathy 11', 'arrhythmogenic right ventricular dysplasia 11 with mild palmoplantar keratoderma and wooly hair', 'familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in DSC2', 'arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and woolly hair', 'arrhythmogenic right ventricular dysplasia, familial, 11, with mild palmoplantar keratoderma and wooly hair', 'arrhythmogenic right ventricular dysplasia, familial, type 11', 'familial arrhythmogenic right ventricular dysplasia 11']",0110082,610476,,,,,,C566471,,,,
mondo:0012507,retinal cone dystrophy 4,"['retinal cone dystrophy 4', 'CACNA2D4 cone dystrophy', 'retinal cone dystrophy type 4', 'RCD4', 'cone dystrophy caused by mutation in CACNA2D4']",0081023,610478,,C1864849,,,,C566470,,,,
mondo:0012508,agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome,"['agammaglobulinemia, microcephaly, and severe dermatitis']",,610483,83617,C1864848,,,,C538055,,,,
mondo:0012509,"pigmented nodular adrenocortical disease, primary, 1","['primary pigmented nodular adrenocortical disease caused by mutation in PRKAR1A', 'Cushing syndrome, adrenal, due to PPNAD1', 'PPNAD1', 'pigmented micronodular adrenocortical disease, primary, 1', 'pigmented nodular adrenocortical disease, primary, type 1', 'pigmented nodular adrenocortical disease, primary, 1', 'PRKAR1A primary pigmented nodular adrenocortical disease', 'adrenocortical nodular dysplasia, primary']",,610489,,,,,,C566469,,,,
mondo:0012510,combined oxidative phosphorylation defect type 2,"['MRPS16 combined oxidative phosphorylation deficiency', 'corpus callosum, agenesis of, with Dysmorphism and fatal lactic acidosis', 'combined oxidative phosphorylation deficiency 2', 'combined oxidative phosphorylation deficiency caused by mutation in MRPS16', 'combined oxidative phosphorylation deficiency type 2', 'COXPD2']",0111483,610498,254920,C1864843,"['-0.4514', '0.2625', '0.4858', '-0.2095', '0.009415', '-0.3926', '-0.0914', '0.4336', '-0.3113', '0.1442', '-0.4976', '-0.1953', '0.5884', '-0.3398', '-0.4136', '0.5244', '0.3987', '-0.1542', '-0.2886', '-0.7886', '0.3843', '-0.3796', '0.7354', '0.2157', '-0.1324', '-0.1667', '0.1189', '0.3022', '-0.1017', '-0.2178', '0.3364', '0.5522', '0.9663', '0.2566', '-0.3735', '-0.2427', '0.01659', '0.1069', '-0.06525', '-0.2382', '-0.184', '-0.3083', '-0.12445', '0.618', '-0.5337', '-0.428', '0.00917', '0.6143', '-0.1459', '-0.09924', '-0.4016', '-0.4758', '0.2634', '0.1344', '-0.8105', '-0.0771', '-0.314', '-0.178', '-0.2766', '0.5615', '-0.5303', '-0.2913', '0.02055', '-0.1832', '-0.661', '0.1759', '0.7617', '0.324', '-0.736', '0.4973', '-0.3086', '0.3835', '0.04498', '0.145', '0.2059', '0.0862', '0.142', '-0.3064', '-0.1283', '0.333', '-0.08167', '0.3254', '-0.12256', '0.02855', '-0.1805', '-0.03748', '0.1172', '0.916', '0.5747', '-0.1567', '0.38', '0.4912', '0.6733', '0.02354', '0.6006', '0.523', '-0.08746', '-0.2698', '0.7314', '0.2412']",,,C566468,,,,
mondo:0012511,preterm premature rupture of the membranes,"['PPROM', 'preterm premature rupture of the membranes, susceptibility to', 'preterm premature rupture of the membranes']",0111144,610504,,,"['-0.02695', '0.033', '-0.004818', '-0.01138', '0.03026', '-0.05148', '0.0056', '0.06125', '-0.04355', '-0.0465', '-0.02441', '-0.02658', '0.007454', '0.04034', '-0.0626', '-0.0646', '0.005146', '-0.000316', '-0.01775', '-0.1106', '0.00309', '-0.02826', '0.0465', '-0.02184', '0.02727', '-0.003885', '0.01169', '0.01128', '0.005142', '-0.01874', '0.0624', '-0.03162', '0.05988', '0.0242', '0.004745', '0.01229', '-0.005497', '-0.01204', '0.002726', '-0.0762', '0.03093', '-0.03888', '0.03064', '-0.03558', '0.00039', '-0.0667', '-0.01924', '0.0191', '0.0148', '0.03076', '-0.00616', '-0.0537', '0.0377', '0.009636', '-0.03696', '-0.01984', '0.0727', '-0.03253', '-0.08167', '-0.011765', '0.0218', '0.03958', '-0.02588', '0.006687', '2.66e-05', '0.01303', '0.06696', '0.0919', '-0.08307', '0.09143', '-0.03293', '0.02542', '0.03577', '-0.04825', '-0.00515', '0.03873', '0.03833', '0.0181', '-0.02097', '-0.05505', '-0.03323', '0.02066', '-0.01698', '0.0156', '0.01099', '-0.001286', '0.02065', '0.04672', '0.06396', '-0.003952', '0.01784', '0.0597', '0.001224', '0.0401', '0.0831', '0.02489', '0.03955', '-0.0651', '-0.004723', '-0.004124']",C92862,,C563032,,,,
mondo:0012512,fatal mitochondrial disease due to combined oxidative phosphorylation defect type 3,"['fatal mitochondrial disease due to COXPD3', 'concentric cardiomyopathy, hypotonia, and lactic acidosis', 'TSFM combined oxidative phosphorylation deficiency', 'encephalomyopathy, respiratory failure, and lactic acidosis', 'combined oxidative phosphorylation deficiency caused by mutation in TSFM', 'COXPD3', 'combined oxidative phosphorylation deficiency 3', 'combined oxidative phosphorylation deficiency type 3']",0111486,610505,168566,,"['-0.4907', '0.3787', '-0.07214', '0.1711', '0.05142', '-0.4617', '-0.06152', '0.615', '-0.2656', '0.1907', '-0.305', '-0.1727', '0.01098', '-0.247', '0.1434', '-0.1324', '0.000222', '-0.0696', '-0.2335', '-0.553', '0.07605', '-0.2169', '0.4375', '-0.1322', '-0.1019', '-0.04056', '0.0892', '0.1923', '0.0786', '-0.2351', '0.4456', '0.428', '0.75', '0.4543', '-0.2157', '-0.558', '-0.3281', '-0.2286', '-0.2338', '0.1223', '-0.11224', '-0.3105', '0.2095', '0.1161', '-0.3647', '0.0351', '-0.02403', '0.2988', '-0.2708', '-0.0653', '-0.0664', '-0.005684', '-0.006622', '-0.168', '-0.06305', '-0.563', '0.1776', '-0.1688', '-0.2932', '0.2354', '0.3762', '0.11115', '0.686', '-0.11456', '-0.2472', '-0.1619', '0.554', '0.555', '-0.572', '0.2323', '-0.2092', '-0.1458', '0.1473', '-0.303', '0.369', '0.1224', '-0.2642', '-0.2094', '-0.1426', '0.393', '0.4097', '0.04944', '0.003057', '0.001138', '0.2817', '0.04968', '0.3057', '0.2947', '0.437', '-0.251', '0.675', '0.1409', '-0.272', '-0.0282', '0.666', '0.3943', '0.3884', '-0.2025', '-0.00402', '-0.0747']",,,C566467,,,,
mondo:0012513,maturity-onset diabetes of the young type 7,"['diabetes mellitus MODY type 7', 'type 7 maturity-onset diabetes of the young', 'MODY type 7', 'KLF11 maturity-onset diabetes of the young (disease)', 'maturity-onset diabetes of the young, type VII', 'MODY KLF11 related', 'maturity-onset diabetes of the young, type 7', 'MODY7']",0111106,610508,,C1864839,,,,C566466,,,,
mondo:0012514,hypomyelinating leukodystrophy 5,"['leukodystrophy caused by mutation in FAM126A', 'FAM126A leukodystrophy', 'hypomyelination-congenital cataract syndrome', 'hypomyelination - congenital cataract', 'hypomyelination and congenital cataract', 'leukodystrophy, hypomyelinating, 5', 'HLD5', 'leukodystrophy, hypomyelinating, type 5', 'hypomyelination and congenital cataract: HCC', 'hypomyelinating leukodystrophy type 5']",0060793,610532,85163,C1864663,"['-0.3076', '0.05777', '-0.1945', '0.11865', '0.01381', '-0.4556', '-0.134', '0.9595', '-0.592', '-0.1605', '-0.424', '0.0867', '0.11096', '0.1006', '0.2413', '-0.0878', '0.2952', '-0.2212', '-0.256', '-0.505', '-0.04846', '0.2155', '0.1157', '-0.3215', '0.2438', '-0.10406', '-0.09235', '0.10986', '-0.1805', '0.01385', '0.3882', '0.003395', '-0.1505', '0.1846', '-0.1179', '0.1776', '-0.12225', '-0.3386', '-0.09546', '0.3171', '0.1759', '-0.219', '-0.1462', '0.05', '-0.06085', '0.182', '-0.0929', '0.232', '-0.267', '-0.2239', '-0.1694', '-0.06204', '-0.011116', '-0.1488', '-0.1332', '-0.4514', '0.4197', '0.02882', '0.02594', '0.335', '-0.0961', '-0.279', '0.2168', '0.1699', '-0.348', '-0.006042', '0.2925', '0.643', '-0.4436', '0.04047', '0.0954', '0.12213', '0.2399', '-0.256', '0.3706', '-0.001439', '-0.0581', '0.1002', '-0.2412', '0.1412', '0.02335', '0.1727', '0.2898', '0.4111', '0.1569', '0.1177', '0.1477', '0.4866', '0.2443', '0.143', '0.2275', '0.748', '0.12177', '0.01349', '0.4944', '0.04593', '0.3782', '-0.4592', '0.10284', '-0.02408']",,,C567166,341.8,,,
mondo:0012515,"glaucoma 1, open angle, M","['JOAG1M', 'GLC1M', 'glaucoma 1, open angle, M']",,610535,,C1864653,,,,C566436,,,,
mondo:0012516,mandibulofacial dysostosis-microcephaly syndrome,"['Growth delay-intellectual disability-mandibulofacial dysostosis-microcephaly-cleft palate syndrome', 'MFDGA', 'mandibulofacial dysostosis, Guion-Almeida type', 'mandibulofacial dysostosis with microcephaly', 'MFDM syndrome', 'Growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palate', 'Growth and intellectual disability, mandibulofacial dysostosis, microcephaly, and cleft palate', 'Growth delay - intellectual disability - mandibulofacial dysostosis - microcephaly - cleft palate', 'MFDM']",0080196,610536,79113,C1864652,"['0.5103', '0.4102', '0.527', '-0.4116', '0.6753', '0.1523', '0.9023', '0.749', '-0.7656', '-0.0822', '0.5317', '-0.419', '0.499', '0.4534', '0.0502', '-0.594', '0.0792', '-0.3599', '-0.6104', '-0.556', '0.1935', '0.1713', '0.22', '-0.0673', '0.402', '0.4497', '-0.6406', '0.2893', '0.5977', '-0.2837', '-0.06384', '-0.3464', '0.4612', '-0.0929', '0.00576', '0.1965', '-0.8066', '-0.11035', '-0.558', '-0.1556', '0.1849', '0.2954', '-0.3315', '-0.655', '0.02773', '-0.0651', '0.5205', '0.382', '-0.5117', '0.07916', '-0.0432', '-0.881', '-0.0907', '-0.174', '-0.516', '0.010086', '-0.8013', '0.3604', '-0.01154', '0.1948', '0.3174', '0.5933', '-0.05554', '-0.011475', '-0.03323', '-0.2524', '0.0695', '0.0816', '-0.74', '0.1719', '-0.732', '1.0', '0.0386', '-0.645', '0.0997', '0.1697', '0.5806', '-0.8066', '-0.675', '-0.211', '-0.4084', '0.382', '0.3105', '0.4475', '-0.038', '-0.4316', '0.1046', '-0.02551', '0.529', '0.652', '0.04968', '0.0584', '-0.2145', '0.2935', '0.2869', '-0.2384', '1.059', '-0.641', '0.836', '-0.638']",,,C537405,,,,
mondo:0012517,Gaucher disease due to saposin C deficiency,"['Gaucher disease, atypical', 'Gaucher disease, atypical, due to saposin C deficiency', 'atypical Gaucher disease due to saposin C deficiency', 'Gaucher disease caused by mutation in PSAP', 'atypical Gaucher^s disease due to saposin c deficiency', 'PSAP Gaucher disease']",0110961,610539,309252,C1864651,"['-0.2742', '0.625', '0.06274', '-0.6416', '-0.203', '-0.1927', '-0.1501', '0.571', '-1.241', '-0.0791', '-0.0824', '0.1731', '-0.2773', '0.699', '0.4153', '-0.5425', '-0.1552', '0.543', '-0.681', '-0.4087', '-0.3835', '-0.5767', '0.2163', '-0.2664', '0.0604', '-0.1625', '0.04016', '0.2227', '0.44', '-0.259', '0.507', '-0.1276', '0.519', '0.0792', '0.1603', '0.09375', '-0.4446', '-0.467', '0.1812', '-0.3035', '0.2812', '-0.367', '-0.3674', '-0.2424', '-0.652', '-0.1865', '-0.1924', '-0.3499', '0.2343', '0.1737', '0.6055', '0.2722', '0.767', '0.032', '0.3716', '-0.512', '-0.1915', '0.4038', '0.2366', '-0.1526', '-0.2656', '-0.2251', '0.1902', '-0.7515', '-0.1317', '0.4219', '-0.1572', '0.06824', '-0.697', '0.03958', '0.1658', '0.06696', '-0.08496', '-0.1766', '0.5024', '-0.1089', '-0.1976', '0.5386', '0.05997', '-0.523', '-0.3914', '-0.5996', '-0.00803', '-0.4612', '-0.4158', '-0.54', '0.7754', '0.0741', '0.576', '0.06445', '-0.51', '-0.34', '0.1171', '0.469', '0.7407', '1.537', '-0.301', '-0.238', '0.1718', '-0.777']",,,C566435,,,,
mondo:0012518,congenital myasthenic syndrome 12,"['congenital myasthenic syndromes with glycosylation defect caused by mutation in GFPT1', 'congenital myasthenic syndrome type 12', 'congenital myasthenia 12 with tubular aggregates', 'myasthenia, congenital, 12, with tubular aggregates', 'GFPT1 congenital myasthenic syndromes with glycosylation defect', 'myasthenic syndrome, congenital, type 12', 'myasthenic syndrome, congenital, with tubular aggregates 1', 'CMS12', 'myasthenic syndrome, congenital, 12']",0110660,610542,,,,C168997,,,,,,
mondo:0012519,Rubinstein-Taybi syndrome due to 16p13.3 microdeletion,"['16p13.3 deletion syndrome', 'Rubinstein-Taybi deletion syndrome', 'Rsts deletion syndrome', 'chromosome 16p13.3 deletion syndrome', 'chromosome 16p13.3 deletion syndrome, proximal']",,610543,353281,C1864648,,,,,,,,
mondo:0012520,insulin-resistance syndrome type A,"['diabetes mellitus, insulin-resistant, with acanthosis nigricans, type a', 'type A insulin resistance syndrome', 'insulin-resistant acanthosis nigricans, type A', 'insulin resistant diabetes mellitus with acanthosis nigricans and hyperandrogenism', 'insulin receptor, defect in, with insulin-resistant diabetes mellitus and acanthosis nigricans', 'Iran, type a', 'diabetes mellitus, insulin-resistant, with acanthosis nigricans']",,610549,2297,,"['0.1649', '0.2338', '0.06476', '-0.267', '0.2021', '-0.883', '0.355', '0.05246', '-0.214', '-0.776', '-0.0968', '-0.215', '0.02249', '-0.013794', '-0.63', '-0.2411', '0.0823', '0.4495', '-0.2291', '-0.6074', '0.1135', '-0.2664', '0.8047', '-0.307', '0.0709', '0.6147', '0.2446', '-0.5244', '0.5483', '-0.747', '0.952', '-0.1007', '0.4226', '0.03522', '0.008', '0.393', '-0.5405', '0.0746', '-0.6377', '0.0082', '0.2455', '-0.2544', '-0.0861', '0.3623', '0.608', '-0.2815', '0.4048', '0.1338', '0.4277', '0.563', '-0.01557', '0.1729', '0.457', '-0.1925', '-0.1818', '-0.02295', '0.0908', '-0.3628', '-0.5303', '0.1816', '0.2844', '0.2788', '0.4116', '-0.519', '-0.11237', '0.3528', '-0.3787', '-0.11743', '-0.6035', '0.3809', '-0.4177', '-0.07385', '0.5522', '0.2196', '0.876', '-0.1832', '-0.618', '-0.0355', '0.2837', '-0.10406', '0.1531', '-0.05673', '-0.2229', '-0.343', '-0.5645', '0.0838', '0.286', '0.3186', '0.623', '0.195', '0.5063', '0.252', '0.536', '-0.05228', '0.1393', '-0.532', '0.105', '-0.427', '-0.6035', '0.278']",C131836,1001503,C562710,,,,
mondo:0012521,herpes simplex encephalitis,"['herpetic encephalitis', 'Herpes simplex virus encephalitis', 'HSE', 'HSV encephalitis', 'Herpes simplex neuroinvasion', 'HSVE', 'Simplexvirus caused infectious encephalitis', 'Herpes simplex meningo-encephalitis']",,,1930,,"['0.3357', '0.717', '-0.1931', '0.1295', '-0.619', '0.0056', '0.512', '-0.456', '-0.1028', '-0.1973', '-0.2017', '0.266', '0.1332', '0.1296', '-0.1505', '0.5786', '-0.8174', '0.1079', '-0.742', '-0.501', '-0.1652', '-0.836', '0.4128', '0.1204', '0.1973', '-0.8945', '-0.371', '0.519', '-0.1299', '-0.1656', '-0.1648', '-0.397', '0.332', '-0.0805', '0.2401', '0.4792', '-0.652', '-0.1765', '0.085', '-0.18', '0.4211', '-0.4358', '0.562', '-0.2401', '-0.0475', '0.516', '-0.2388', '-0.014084', '-0.129', '1.029', '-0.1409', '-0.318', '-0.1836', '0.291', '-0.000725', '-0.0585', '-0.1776', '-0.0497', '-0.3596', '-0.2979', '-0.756', '0.09076', '-0.74', '0.2603', '-0.003494', '0.007904', '0.12164', '0.3052', '-0.5054', '0.517', '-0.2815', '0.4236', '0.4375', '-0.4731', '0.1299', '0.4727', '0.2269', '-0.1073', '-0.10406', '-0.1294', '0.4485', '-0.3643', '-0.311', '0.0092', '0.4443', '-0.2542', '0.549', '0.7217', '0.2278', '0.318', '0.3215', '0.3718', '-0.01749', '-0.06793', '0.1813', '0.472', '0.2869', '-0.328', '0.1263', '-0.7466']",C84762,,D020803,,,,
mondo:0012522,"diabetes mellitus, transient neonatal, 3","['Tndm3', 'KCNJ11 transient neonatal diabetes mellitus (disease)', 'diabetes mellitus, transient neonatal, 3', 'diabetes mellitus, transient neonatal, type 3', 'diabetes mellitus, transient neonatal 3', 'diabetes mellitus, type II, autosomal dominant']",,610582,,,,,,C566432,,,,
mondo:0012523,retinitis pigmentosa 36,"['RP 36', 'retinitis pigmentosa type 36', 'retinitis pigmentosa 36', 'retinitis pigmentosa caused by mutation in PRCD', 'RP36', 'PRCD retinitis pigmentosa']",0110405,610599,,C1864621,,,,C566431,,H35.5,,
mondo:0012524,corticosterone methyloxidase type 2 deficiency,"['steroid 18-oxidase deficiency', 'hyperreninemic hypoaldosteronism, familial, 1', 'Cmo 2 deficiency', 'corticosterone methyloxidase type II deficiency', '18-oxidase deficiency', 'aldosterone deficiency due to deficiency of steroid 18-oxidase', 'hypoaldosteronism, congenital, due to CMO II deficiency', 'aldosterone deficiency 2']",,610600,,C3463917,,,,,,,,
mondo:0012525,Leber congenital amaurosis 12,"['LCA12', 'Leber congenital amaurosis caused by mutation in RD3', 'RD3 Leber congenital amaurosis', 'amaurosis congenita of Leber, type 12', 'Leber congenital amaurosis 12', 'Leber congenital amaurosis type 12']",0110080,610612,,,,,,C565697,,H35.5,,
mondo:0012526,hereditary angioedema type 3,"['HAE 3', 'inherited estrogen-associated angioedema', 'hereditary angioneurotic oedema type 3', 'estrogen-related Hae', 'hereditary angioneurotic edema type 3', 'angioedema, hereditary, type III', 'estrogen-sensitive Hae', 'inherited estrogen-associated angioneurotic edema', 'inherited estrogen-associated angioneurotic oedema', 'Hae with normal C1 inhibitor concentration and function', 'hereditary angioedema with normal C1 inhibitor activity', 'F12 hereditary angioedema', 'Hae 3', 'inherited estrogen-dependent angioedema', 'angioedema, hereditary, 3', 'angioedema, hereditary, type 3', 'HAE-III', 'HAE3', 'angioneurotic edema, hereditary, with normal C1 inhibitor concentration and function', 'inherited estrogen-dependent angioneurotic oedema', 'hereditary angioedema caused by mutation in F12', 'inherited estrogen-dependent angioneurotic edema']",0080940,610618,100054,,"['0.5596', '-0.2678', '-0.4382', '-0.1823', '-0.0631', '-0.1748', '-0.2042', '0.2448', '-0.726', '0.3877', '-0.3645', '0.2377', '0.285', '0.02907', '-0.432', '-0.0836', '0.2905', '0.1008', '-0.1471', '-0.0697', '0.1069', '-0.4412', '1.213', '-0.402', '-0.4714', '0.1428', '-0.1653', '-0.353', '0.03065', '-0.2568', '0.3328', '0.4436', '0.2386', '-0.1887', '-0.1683', '-0.1373', '-0.0267', '0.228', '-0.06335', '0.233', '0.4', '-0.3057', '-0.1829', '-0.3032', '0.04547', '-0.11176', '0.01149', '0.1848', '-0.02365', '0.1265', '-0.01176', '-0.4277', '0.2502', '-0.2847', '-0.3416', '0.5195', '0.4429', '-1.12', '-0.5806', '-0.1055', '0.1608', '0.4424', '0.336', '-0.3982', '0.1957', '0.02437', '0.468', '0.08765', '-0.545', '0.662', '0.1986', '-0.2693', '-0.4827', '-0.4048', '0.3135', '0.247', '0.325', '0.0816', '-0.5093', '-0.053', '-0.014854', '0.01041', '0.2705', '0.32', '-0.371', '0.3218', '0.295', '0.3171', '0.1514', '-0.0788', '0.3528', '-0.1086', '0.2847', '0.06915', '0.836', '0.2583', '0.4148', '-0.0888', '-1.006', '-0.12415']",,,D056828,277.6,,,
mondo:0012527,cataract 11 multiple types,"['posterior polar cataract 4', 'cataract 11, multiple types', 'CPP4', 'PITX3 early-onset non-syndromic cataract', 'early-onset non-syndromic cataract caused by mutation in PITX3', 'cataract, posterior polar, 4', 'cataract 11 with microphthalmia and neurodevelopmental abnormalities', 'CTPP4', 'Posterior polar cataract, 4', 'Cpp4', 'cataract 11, syndromic, autosomal recessive', 'CTRCT11']",0110249,610623,98993,,,,,C535344,,,,
mondo:0012528,hypogonadotropic hypogonadism 4 with or without anosmia,"['hypogonadotropic hypogonadism 4 with or without anosmia', 'Kallman syndrome 4', 'Kallmann syndrome 4', 'PROK2 hypogonadotropic hypogonadism', 'KAL4', 'hypogonadotropic hypogonadism caused by mutation in PROK2', 'HH4']",0090077,610628,,C3552343,,,,C565696,,E23.0,,
mondo:0012529,Diamond-Blackfan anemia 3,"['RPS24 Diamond-Blackfan anaemia', 'anemia Diamond-Blackfan 3', 'DBA3', 'RPS24 Diamond-Blackfan anemia', 'Diamond-Blackfan Anaemia type 3', 'Diamond-Blackfan anemia 3', 'anaemia Diamond-Blackfan 3', 'Diamond-Blackfan anemia caused by mutation in RPS24', 'Diamond-Blackfan anaemia caused by mutation in RPS24', 'Diamond-Blackfan Anemia type 3']",0111887,610629,,C1857719,,C176912,,C536355,,,,
mondo:0012530,palmoplantar keratoderma-XX sex reversal-predisposition to squamous cell carcinoma syndrome,"['palmoplantar hyperkeratosis-XX sex reversal-predisposition to squamous cell carcinoma syndrome', 'palmoplantar hyperkeratosis with squamous cell carcinoma of skin and 46,XX SEX reversal', 'palmoplantar hyperkeratosis and true hermaphroditism', 'palmoplantar hyperkeratosis with squamous cell carcinoma of skin and sex reversal']",,610644,85112,,"['-0.02762', '0.2361', '-0.2869', '-0.0854', '0.2893', '-0.4893', '-0.03458', '0.285', '0.0378', '-0.4746', '0.13', '-0.2996', '-0.2318', '-0.1512', '0.0274', '-0.1111', '0.4355', '-0.0786', '-0.03146', '-0.3997', '-0.387', '0.0338', '0.3804', '-0.4978', '0.5024', '0.04202', '-0.3215', '0.1979', '-0.03053', '-0.5225', '0.4114', '-0.2019', '0.4438', '-0.307', '0.02226', '-0.1714', '0.1483', '-0.551', '-0.3037', '-0.02887', '0.0875', '-0.344', '-0.24', '-0.39', '-0.0388', '-0.1984', '-0.3765', '-0.08246', '-0.2917', '-0.23', '0.02657', '-0.1603', '-0.06015', '0.2411', '-0.3706', '0.06744', '0.457', '-0.1186', '-0.4172', '-0.03824', '0.3235', '0.1344', '-0.068', '0.091', '0.2494', '0.06174', '0.3103', '0.301', '-0.3428', '0.3445', '-0.2219', '-0.03055', '-0.005985', '0.1635', '0.1492', '-0.1532', '-0.2157', '-0.109', '-0.1954', '-0.1356', '-0.01512', '0.773', '-0.122', '-0.03375', '-0.03702', '-0.0916', '0.1471', '0.2225', '0.3696', '-0.1515', '0.1733', '0.298', '0.1241', '-0.1348', '0.5273', '-0.05856', '0.2722', '-0.5444', '-0.0207', '-0.1073']",,,C567165,,,,
mondo:0012531,xeroderma pigmentosum group B,"['ERCC3 xeroderma pigmentosum', 'xeroderma pigmentosum, type 2', 'XPB', 'XPB/CS', 'XP, Group B', 'xeroderma pigmentosum caused by mutation in ERCC3', 'xeroderma pigmentosum B/Cockayne syndrome', 'xeroderma pigmentosum, complementation group B', 'xeroderma pigmentosum, complementation group type B', 'xeroderma pigmentosum, group B', 'XP group B', 'XPBC', 'xeroderma pigmentosum group type B', 'XP-B']",0110850,610651,276252,C0268136,"['-0.266', '0.311', '-0.11176', '0.1969', '0.2793', '-0.2996', '-0.01501', '-0.2517', '-0.03143', '-0.2708', '0.0239', '0.165', '-0.0729', '0.06506', '-0.0992', '-0.0981', '-0.0405', '-0.1247', '0.04883', '-0.3625', '0.002586', '-0.12256', '0.08276', '0.0395', '-0.02553', '0.1229', '0.01407', '0.1729', '-0.01537', '0.01111', '0.1365', '0.1081', '0.156', '0.0677', '0.2048', '-0.03137', '0.1956', '-0.3042', '-0.1387', '-0.58', '0.1536', '-0.5425', '0.096', '0.03156', '-0.3647', '-0.589', '0.1191', '-0.0741', '0.5063', '-0.03043', '0.2903', '-0.318', '0.0975', '0.1621', '-0.11725', '-0.4114', '0.5786', '0.229', '-0.4968', '-0.10565', '0.1704', '-0.0158', '-0.015305', '0.1864', '0.2145', '0.2472', '0.3574', '0.01307', '-0.06793', '0.1691', '-0.6123', '-0.00572', '0.257', '-0.0055', '0.2468', '0.096', '0.06665', '0.0535', '-0.0647', '-0.1812', '-0.04346', '0.044', '-0.115', '0.1871', '0.01269', '-0.2217', '0.389', '0.4277', '0.2424', '0.09296', '0.3555', '0.1893', '-0.02707', '-0.24', '0.269', '0.2251', '0.2847', '-0.4673', '-0.02565', '0.0506']",C3966,,C562590,,,,
mondo:0012532,hereditary hemorrhagic telangiectasia type 4,"['telangiectasia, hereditary hemorrhagic, type 4', 'HHT4']",,610655,,,,,,C565691,,,,
mondo:0012533,"autism, susceptibility to, 7","['autism susceptibility 7', 'AUTS7', 'autism, susceptibility to, 7']",,610676,,,,,,,,,,
mondo:0012534,combined oxidative phosphorylation defect type 4,"['combined oxidative phosphorylation deficiency 4', 'combined oxidative phosphorylation deficiency type 4', 'combined oxidative phosphorylation deficiency caused by mutation in TUFM', 'COXPD4', 'TUFM combined oxidative phosphorylation deficiency']",0111494,610678,254925,C1857682,"['-0.797', '-0.01093', '-0.036', '-0.1476', '0.00771', '-0.357', '0.006226', '0.3147', '-0.2039', '0.614', '-0.5127', '-0.6157', '0.3936', '-0.4517', '0.1506', '-0.02438', '0.2108', '-0.1636', '-0.347', '-0.957', '0.241', '-0.4666', '0.5527', '-0.2224', '0.05435', '-0.349', '0.2573', '0.4014', '-0.4368', '-0.1266', '-0.03812', '0.532', '1.125', '0.1593', '0.03836', '-0.2219', '-0.1184', '-0.10767', '0.0895', '-0.2311', '0.2184', '-0.4927', '-0.06122', '0.56', '-0.3699', '-0.4404', '-0.0546', '0.239', '-0.1327', '-0.1399', '-0.4102', '-0.1772', '-0.1039', '-0.08734', '-0.2327', '-0.0909', '0.276', '-0.5356', '-0.1344', '0.1791', '0.1261', '-0.204', '0.5977', '0.08167', '-1.192', '-0.0411', '0.9775', '0.609', '-0.448', '0.1974', '0.08044', '0.5063', '-0.3108', '-0.01727', '0.1511', '-0.1349', '0.5405', '0.004795', '-0.362', '0.3745', '-0.1542', '0.1885', '0.3079', '0.3645', '-0.3557', '-0.1846', '0.2354', '0.5215', '0.184', '-0.1803', '0.6177', '0.3135', '0.2417', '0.3254', '0.44', '0.685', '0.194', '-0.1274', '0.2847', '0.3315']",,,C565690,,,,
mondo:0012535,"holoprosencephaly, recurrent infections, and monocytosis","['holoprosencephaly, recurrent infections, and monocytosis']",,610680,,C1853187,,,,C538328,,,,
mondo:0012536,osteogenesis imperfecta type 7,"['OI type VII', 'osteogenesis imperfecta caused by mutation in CRTAP', 'OI, type 7', 'osteogenesis imperfecta, type VII', 'OI7', 'osteogenesis imperfecta, type IIb', 'CRTAP osteogenesis imperfecta', 'osteogenesis imperfecta type VII', 'osteogenesis imperfecta, type IIb, formerly', 'osteogenesis imperfecta, type 7', 'OI type 7']",0110337,610682,216820,C1853162,,,,,,,,
mondo:0012537,split-hand/foot malformation with long bone deficiency 2,"['split-hand/foot malformation with long bone deficiency 2', 'SHFLD2']",,610685,,C1853156,,,,C565199,,,,
mondo:0012538,nemaline myopathy 7,"['nemaline myopathy 7, autosomal recessive', 'CFL2 nemaline myopathy', 'NEM7', 'nemaline myopathy 7', 'nemaline myopathy type 7', 'nemaline myopathy caused by mutation in CFL2']",0110934,610687,,C1853154,,,,C565198,,,,
mondo:0012539,Joubert syndrome 6,"['TMEM67 Joubert syndrome', 'Joubert syndrome caused by mutation in TMEM67', 'JBTS6', 'Joubert syndrome type 6', 'Joubert syndrome 6']",0111001,610688,,C1853153,,,,C537689,,,,
mondo:0012540,age related macular degeneration 4,"['age related macular degeneration type 4', 'ARMD4', 'macular Degeneration, age-related, type 4', 'macular degeneration, age-related, 4', 'CFH age-related macular degeneration', 'age-related macular degeneration caused by mutation in CFH']",0110017,610698,,C1853147,,,,C565196,,,,
mondo:0012541,"deafness with labyrinthine aplasia, microtia, and microdontia","['deafness with labyrinthine aplasia microtia and microdontia (LAMM)', 'LAMM syndrome', 'deafness, congenital with inner ear agenesis, microtia, and microdontia', 'congenital deafness with inner ear agenesis microtia and microdontia', 'deafness, congenital, with labyrinthine aplasia, microtia, and microdontia', 'deafness congenital with inner ear agenesis microtia and microdontia', 'deafness, congenital, with inner EAR agenesis, microtia, and microdontia', 'deafness with Lamm', 'microdontia-type I microtia-deafness syndrome']",,610706,90024,C1853144,"['-0.007587', '0.2983', '0.04797', '0.05835', '0.618', '-0.3804', '0.2347', '0.4492', '-0.1893', '-0.219', '-0.4753', '-0.7275', '-0.00636', '-0.271', '0.05594', '-0.111', '0.4014', '-0.0511', '-0.2712', '-0.1166', '-0.3137', '0.1619', '0.2306', '-0.1296', '0.695', '0.2576', '-0.693', '0.3286', '0.1904', '-0.7456', '0.3394', '0.5596', '-0.0371', '-0.0323', '-0.02246', '-1.109', '-0.03223', '-0.1707', '-0.358', '-0.7354', '0.004627', '-0.02376', '-0.04504', '-0.5776', '-0.3516', '-0.9126', '0.07886', '0.4067', '0.02934', '-0.3882', '-0.0987', '-0.584', '-0.04636', '-0.338', '-0.06793', '-0.3237', '0.668', '0.1954', '-0.1006', '0.2883', '-0.2664', '0.02802', '0.03894', '0.1089', '-0.348', '-0.3862', '-0.07666', '0.537', '-0.1741', '0.5825', '-0.292', '-0.03494', '0.2966', '-0.3271', '0.1608', '-0.3198', '0.258', '0.05826', '-0.1169', '0.2316', '0.437', '0.2316', '-0.1932', '0.602', '-0.2803', '-0.2008', '0.1405', '1.165', '0.0737', '0.3362', '-0.626', '0.7476', '-0.1686', '-0.01191', '0.9307', '-0.12085', '0.3965', '-0.781', '0.0667', '0.198']",,,C565195,759.89,,,
mondo:0012542,"psoriasis 8, susceptibility to","['psoriasis susceptibility 8', 'PSORS8', 'psoriasis 8, susceptibility to']",0111288,610707,,,,,,,,,,
mondo:0012543,optic atrophy 5,"['OPA5', 'optic atrophy 5']",0111438,610708,,C1853139,,,,C537126,,,,
mondo:0012544,brachydactyly-syndactyly syndrome,"['brachydactyly-syndactyly syndrome', 'Bdsd', 'BDSD', 'brachydactyly-syndactyly, Zhao type', 'brachydactyly-syndactyly-oligodactyly syndrome']",0050689,610713,93409,C1853137,"['-0.0382', '0.113', '0.02002', '-0.02048', '0.1382', '-0.3208', '-0.0813', '0.645', '-0.3054', '-0.4346', '-0.3333', '-0.1776', '-0.1685', '-0.0187', '-0.145', '-0.127', '0.4092', '-0.1262', '-0.01046', '-0.3442', '-0.24', '-0.03082', '0.3413', '-0.253', '0.4258', '0.212', '-0.2559', '0.2358', '0.0932', '-0.349', '0.4216', '-0.4473', '-0.0608', '0.12024', '0.4104', '-0.3428', '0.0654', '-0.3464', '-0.02315', '-0.1231', '-0.09955', '-0.3826', '0.144', '0.03244', '0.288', '-0.1421', '-0.00794', '0.594', '-0.04388', '-0.2903', '0.1714', '-0.11', '-0.09906', '-0.1436', '-0.35', '-0.526', '0.08966', '-0.233', '-0.03226', '0.02696', '0.0898', '-0.02765', '-0.01066', '0.0963', '-0.1581', '0.11584', '0.1619', '0.1204', '-0.2546', '0.1506', '-0.3154', '0.1537', '0.1754', '-0.2076', '0.3274', '0.3113', '-0.279', '-0.0722', '-0.4128', '-0.05493', '-0.13', '0.2705', '-0.007664', '0.2979', '0.1555', '-0.1268', '-0.1833', '0.6035', '0.2283', '-0.3848', '-0.1442', '0.4773', '0.2793', '-0.1207', '0.607', '-0.1079', '0.2461', '-0.818', '0.2296', '0.1226']",,,C565193,,,,
mondo:0012545,neutral lipid storage myopathy,"['neutral lipid storage disease with myopathy', 'triglyceride deposit cardiomyovasculopathy', 'neutral lipid storage disease without ichthyosis', 'NLSDM', 'neutral lipid storage disease with myopathy without ichthyosis']",,610717,98908,,"['-0.2651', '0.3506', '0.07794', '-0.2607', '-0.04056', '-0.423', '-0.1567', '0.2406', '-0.298', '0.1473', '-0.391', '0.08887', '0.1026', '0.1667', '-0.1837', '-0.1935', '-0.289', '-0.00898', '-0.1974', '-0.3845', '0.2147', '-0.3643', '0.3962', '0.351', '0.010086', '0.12177', '0.0721', '0.03192', '-0.2588', '-0.1571', '0.6245', '0.009285', '0.3901', '0.278', '0.1323', '-0.15', '-0.4775', '0.1564', '0.00561', '-0.5244', '-0.519', '-0.3118', '0.0747', '0.523', '-0.2822', '0.05392', '0.04395', '0.2673', '-0.2554', '0.06714', '-0.155', '0.4636', '0.1346', '-0.0865', '-0.0944', '-0.4453', '0.1476', '-0.3494', '-0.3142', '0.03903', '0.255', '-0.02353', '-0.008896', '-0.2158', '-0.3704', '-0.2942', '0.3066', '0.3394', '-0.1426', '-0.02051', '-0.4055', '-0.098', '0.152', '0.2925', '0.2854', '-0.03192', '-0.0718', '0.1962', '-0.00763', '-0.324', '-0.04556', '-0.04175', '0.05182', '0.1257', '0.00825', '0.3467', '0.04965', '0.04492', '0.334', '-0.1731', '0.647', '0.156', '-0.07495', '-0.02066', '0.5728', '0.2365', '0.3696', '-0.0802', '-0.2837', '0.1544']",,,,,,,
mondo:0012546,"nephrotic syndrome, type 3","['nephrotic syndrome, early-onset, type 3', 'PLCE1 nephrotic syndrome', 'nephrotic syndrome, type 3', 'NPHS3', 'nephrotic syndrome caused by mutation in PLCE1']",0080382,610725,,C1853124,,,,,,,,
mondo:0012547,Noonan syndrome 4,"['Noonan syndrome type 4', 'SOS1 Noonan syndrome', 'Noonan syndrome 4', 'SOS1 gene related Noonan syndrome', 'Noonan syndrome caused by mutation in SOS1', 'NS4']",0060582,610733,,C1853120,,C176932,,C548082,,,,
mondo:0012548,Kostmann syndrome,"['infantile agranulocytosis', 'Kostmann disease', 'neutropenia, severe congenital 3, autosomal recessive', 'agranulocytosis infantile', 'SCN3', 'severe congenital neutropenia autosomal recessive 3', 'neutropenia, severe congenital, 3, autosomal recessive', 'agranulocytosis, infantile', 'severe congenital neutropenia type 3']",0112133,610738,99749,CN032247,"['-0.11554', '-0.0894', '0.3203', '-0.5396', '-0.01418', '-0.2388', '0.2874', '0.3142', '0.0465', '-0.3367', '-0.05722', '-0.428', '-0.3594', '-0.1443', '0.10834', '-0.1842', '-0.1844', '0.3806', '-0.1934', '-0.352', '0.1089', '-0.1898', '0.3496', '-0.5005', '0.04477', '-0.1708', '-0.216', '-0.2646', '-0.1888', '-0.312', '0.02603', '0.1821', '0.2203', '0.2322', '0.0932', '-0.0957', '-0.549', '-0.4858', '-0.1989', '-0.2764', '-0.0692', '-0.2964', '0.0704', '-0.2998', '-0.273', '-0.453', '-0.1919', '0.1223', '-0.004845', '0.2607', '-0.05154', '0.4285', '0.109', '0.10236', '0.0365', '0.314', '0.2007', '-0.509', '-0.306', '-0.0625', '0.0389', '0.4973', '-0.251', '-0.3354', '0.3726', '-0.3875', '0.2096', '0.1465', '-0.2341', '0.3335', '-0.275', '-0.05487', '-0.3208', '-0.1471', '0.07245', '-0.07697', '0.4087', '-0.0884', '0.2445', '0.00864', '-0.3042', '-0.1877', '0.0447', '0.39', '-0.1527', '0.007595', '0.1079', '0.2986', '0.1133', '-0.2441', '0.354', '0.1749', '-0.0991', '0.11816', '0.562', '0.708', '0.4585', '-0.2455', '-0.1135', '0.001118']",,,,,,,
mondo:0012549,"autosomal recessive ataxia, Beauce type","['ataxia, recessive, of Beauce', 'spinocerebellar ataxia, autosomal recessive type 8', 'cerebellar ataxia, autosomal recessive, type 1', 'autosomal recessive spinocerebellar ataxia 8', 'SCAR8', 'recessive ataxia of Beauce', 'autosomal recessive ataxia Beauce type', 'spinocerebellar ataxia autosomal recessive 8', 'spinocerebellar ataxia, autosomal recessive 8', 'ARCA1', 'autosomal recessive cerebellar ataxia type 1', 'SYNE1-related autosomal recessive cerebellar ataxia']",0111618,610743,88644,C3683483,"['-0.143', '-0.3376', '-0.002792', '0.1407', '-0.1626', '-1.042', '0.219', '-0.0546', '-0.577', '-0.927', '0.09283', '0.126', '-0.2952', '0.07184', '0.569', '-0.2494', '-0.1365', '-0.2644', '-0.0759', '-1.034', '-0.1052', '-0.3362', '0.2329', '-0.688', '0.5923', '-0.538', '-0.3965', '0.2325', '-0.172', '-0.908', '0.0748', '0.4846', '-0.6333', '-0.04236', '0.4753', '0.0349', '-0.2181', '0.05756', '0.5625', '0.3767', '0.2764', '0.2135', '-0.3545', '0.4155', '0.7', '-0.6826', '0.2126', '0.4622', '0.471', '-0.1328', '-0.1301', '0.21', '-0.05444', '-0.4094', '-0.10175', '-0.8', '0.4512', '0.5967', '-0.04477', '0.4644', '-0.589', '0.2072', '0.3086', '-0.1418', '-0.5894', '0.5425', '0.3057', '0.614', '-0.622', '0.3933', '0.8804', '0.4353', '-0.0545', '-0.7056', '0.7544', '0.398', '0.2786', '0.4023', '0.2478', '0.4924', '-0.4355', '-0.7134', '0.3804', '0.8354', '-0.255', '-0.7163', '0.2793', '0.0785', '0.4958', '0.4912', '0.3005', '0.5176', '0.0812', '0.0852', '1.054', '1.157', '0.3066', '0.3845', '-0.4724', '0.00935']",,,,,,,
mondo:0012550,iris pattern,['iris pattern'],,610744,,C1853115,,,,,,,,
mondo:0012551,alopecia areata 2,"['AA2', 'alopecia areata 2']",,610753,701,C1853104,,,,C565186,,,,
mondo:0012552,multiple endocrine neoplasia type 4,"['CDKN1B multiple endocrine neoplasia', 'multiple endocrine neoplasia, type IV', 'MEN4', 'multiple endocrine neoplasia caused by mutation in CDKN1B', 'multiple endocrine neoplasia, type 4']",0080137,610755,276152,C4274947,"['0.0679', '0.2678', '-0.4136', '-0.4158', '-0.07336', '-0.1423', '0.3071', '0.1658', '-0.315', '-0.6025', '0.1731', '0.01341', '-0.2842', '0.4236', '-0.3586', '-0.9624', '-0.1077', '-0.05557', '-0.05005', '-0.2656', '-0.1283', '-0.4485', '0.4287', '-0.605', '0.2715', '0.446', '-0.53', '-0.4692', '0.1768', '-0.505', '0.425', '-0.09875', '0.4177', '-0.557', '0.07214', '-0.2966', '-0.69', '-0.0989', '-0.2515', '0.2625', '0.08246', '-0.4421', '0.5566', '-0.4678', '0.7617', '-0.2291', '0.1627', '0.2473', '0.1677', '-0.2783', '0.4507', '0.4507', '-0.01561', '-0.272', '-0.642', '-0.1029', '0.3323', '-0.1902', '-0.3176', '0.4163', '0.5654', '0.2019', '-0.234', '-0.036', '0.04834', '0.2109', '0.1766', '0.7964', '-0.7314', '0.4268', '0.1886', '0.0874', '0.5293', '0.02428', '0.6655', '0.544', '-0.8584', '0.1783', '-0.558', '-0.02187', '-0.06506', '0.6533', '0.2103', '-0.0752', '0.0009356', '-0.3894', '0.4678', '-0.336', '0.3914', '-0.635', '0.4033', '-0.05353', '0.3477', '-0.5537', '0.8735', '-0.0376', '0.3965', '-0.199', '0.005886', '0.1931']",C157449,,C567059,,,,
mondo:0012553,cerebrooculofacioskeletal syndrome 2,"['ERCC2 COFS syndrome', 'COFS2', 'cerebrooculofacioskeletal syndrome type 2', 'COFS syndrome caused by mutation in ERCC2', 'cerebrooculofacioskeletal syndrome 2']",0080912,610756,,C1853102,,,,C565185,,,,
mondo:0012554,cerebrooculofacioskeletal syndrome 4,"['COFS4', 'COFS syndrome caused by mutation in ERCC1', 'cerebrooculofacioskeletal syndrome 4', 'cerebrooculofacioskeletal syndrome type 4', 'ERCC1 COFS syndrome']",0080914,610758,,C1853100,,C173104,,C565184,,,,
mondo:0012555,Cornelia de Lange syndrome 3,"['Cornelia de Lange syndrome caused by mutation in Smc3', 'Cornelia DE Lange syndrome 3', 'CDLS3', 'Smc3 Cornelia de Lange syndrome', 'Cornelia De Lange syndrome type 3', 'SMC3 Cornelia de Lange syndrome', 'Cornelia de Lange syndrome 3']",0080507,610759,,C1853099,,,,,,,,
mondo:0012556,DK1-congenital disorder of glycosylation,"['CDG1M', 'DOLK-CDG (CDG-Im)', 'dolichol kinase deficiency', 'Dk1 deficiency', 'congenital disorder of glycosylation, type Im', 'congenital disorder of glycosylation type Im', 'DK1-CDG', 'CDGIm', 'CDG Im', 'CDG syndrome type Im', 'CDG-Im', 'hypotonia and ichthyosis due to dolichol phosphate deficiency', 'congenital disorder of glycosylation type 1m', 'carbohydrate deficient glycoprotein syndrome type Im']",0080565,610768,91131,,"['-0.2812', '0.3342', '-0.3203', '-0.1931', '0.455', '-0.5967', '-0.0911', '0.739', '-0.3298', '-0.2039', '-0.2482', '0.1471', '0.05072', '-0.1438', '0.06506', '-0.006306', '-0.3352', '-0.437', '-0.683', '-0.2935', '0.0699', '-0.4026', '0.554', '-0.4578', '0.2424', '0.03778', '0.09906', '-0.1084', '-0.10803', '-0.2466', '0.3171', '-0.064', '0.1334', '0.07196', '-0.5825', '-0.1647', '0.3408', '-0.001763', '-0.3533', '-0.05124', '0.1537', '-0.3777', '-0.01683', '0.0397', '-0.3062', '0.1632', '0.1099', '0.2954', '0.05072', '-0.1938', '-0.3833', '-0.4805', '-0.1406', '0.2534', '0.0664', '-0.662', '1.092', '0.03506', '-0.1926', '0.3125', '0.12427', '-0.06995', '0.3503', '0.355', '-0.2201', '0.2014', '0.25', '0.272', '-0.4233', '-0.4607', '-0.347', '0.1473', '-0.087', '0.1738', '0.4358', '0.1268', '-0.1148', '-0.3381', '-0.1715', '0.2432', '0.566', '0.543', '0.1735', '-0.1108', '-0.089', '0.0149', '0.4133', '0.535', '0.1763', '-0.04196', '0.006382', '0.4714', '-0.2402', '-0.2114', '1.076', '0.3228', '0.2384', '-0.743', '-0.1324', '-0.592']",,,C563666,,,,
mondo:0012557,cardiomyopathy-hypotonia-lactic acidosis syndrome,"['Mpcd', 'mitochondrial phosphate carrier deficiency']",,610773,91130,C4305259,"['-0.09454', '-0.738', '-0.061', '0.582', '0.1711', '-0.678', '0.3206', '0.7383', '-0.193', '-0.372', '0.4766', '-0.4287', '-0.169', '0.2384', '-0.549', '0.2512', '-0.5645', '-0.1505', '-0.7246', '-0.751', '0.3076', '0.5522', '0.6167', '0.1938', '0.3518', '-0.3638', '0.074', '0.6265', '-0.05896', '-0.2524', '1.113', '-0.001757', '0.613', '0.3147', '0.03275', '-0.5024', '-0.0769', '-0.502', '0.657', '-0.4211', '-0.0939', '0.4902', '-0.2817', '0.5776', '0.2878', '0.5293', '0.2101', '0.5684', '0.4812', '-0.556', '-0.788', '-0.1742', '0.671', '-0.01278', '0.7783', '-0.5117', '-0.131', '0.5186', '-0.4604', '0.2727', '-0.0917', '0.506', '0.2076', '-0.991', '-0.933', '0.1802', '0.1471', '0.6426', '-1.051', '-0.1886', '-0.4868', '0.1804', '-0.03513', '-0.3367', '-0.1158', '0.7188', '-0.271', '0.1864', '-0.683', '0.718', '0.1703', '-0.0809', '-0.1602', '-0.4692', '1.198', '-0.2094', '0.5317', '0.1884', '0.5425', '0.04282', '0.3418', '0.03864', '0.1127', '-0.0862', '1.003', '0.877', '0.3103', '-0.6357', '-0.4104', '-0.6187']",,,C563665,,,,
mondo:0012558,"epiphyseal dysplasia, Baumann type","['epiphyseal dysplasia, Baumann type']",,610797,,C1835830,,,,C563664,,,,
mondo:0012559,primary immunodeficiency syndrome due to p14 deficiency,"['immunodeficiency due to defect in MAPBP-interacting PROTEIN', 'primary immunodeficiency syndrome with short stature', 'primary immunodeficiency syndrome due to LAMTOR2 deficiency', 'immunodeficiency due to defect in Mapbp-interacting Protein']",,610798,90023,C4305256,"['-0.0992', '0.0444', '0.02394', '0.573', '0.6934', '0.1967', '0.2852', '-0.10706', '0.02478', '-0.033', '-0.01051', '0.1536', '-0.4185', '0.37', '0.563', '0.3865', '-0.1853', '0.495', '-1.342', '-0.332', '0.4631', '0.673', '0.3584', '-0.4722', '0.4119', '-0.4124', '-0.8784', '-0.4004', '0.04538', '-0.731', '0.292', '0.494', '-0.10474', '-0.3762', '0.1118', '-0.03418', '-0.5454', '-0.1503', '-0.1573', '-0.05252', '0.544', '0.2695', '0.06274', '-0.5522', '-0.11365', '-0.594', '-0.0255', '0.1434', '0.441', '0.0636', '-0.602', '-0.2478', '0.466', '-0.1102', '-0.5483', '-0.1053', '-0.784', '-0.01929', '-0.2045', '-0.4333', '-0.2123', '0.5776', '0.02087', '0.4797', '0.5576', '0.2463', '-0.00845', '0.7744', '-0.3271', '0.604', '-0.2666', '-0.12', '-0.2021', '-0.2676', '0.06525', '0.03038', '0.011215', '0.1107', '0.3745', '0.5215', '0.2438', '-0.1133', '0.12085', '0.509', '0.1997', '0.1713', '0.4329', '0.6484', '0.958', '0.04398', '-0.3699', '0.3093', '-0.2222', '-0.0806', '0.4724', '1.021', '-0.2998', '-1.108', '0.03918', '0.2023']",,,C563663,,,,
mondo:0012561,congenital anomalies of kidney and urinary tract 1,"['congenital anomalies of kidney and urinary tract 1', 'renal hypodysplasia, nonsyndromic, 1', 'congenital anomaly of kidney and urinary tract caused by mutation in DSTYK', 'DSTYK congenital anomaly of kidney and urinary tract', 'CAKUT1']",0080206,610805,,C1835826,"['-0.02036', '0.04797', '0.01417', '-0.01955', '0.02722', '-0.04678', '0.01117', '0.071', '-0.04565', '-0.03403', '-0.01657', '-0.02509', '-0.02264', '0.01584', '-0.04395', '-0.036', '-0.01418', '-0.02519', '-0.02608', '-0.1145', '0.00876', '-0.02095', '0.06042', '-0.0218', '0.014465', '-0.0288', '-0.01755', '0.00516', '-0.003187', '-0.02951', '0.0675', '-0.012924', '0.05655', '0.014915', '0.01012', '-0.02245', '-0.03497', '-0.0103', '-0.00991', '-0.0568', '0.02898', '-0.0573', '0.03256', '-0.02705', '-0.01458', '-0.0552', '-0.01392', '0.0331', '0.01796', '0.01987', '-0.02713', '-0.01688', '0.03055', '-0.02626', '-0.03024', '-0.01892', '0.04895', '-0.02266', '-0.0702', '0.007225', '0.04352', '0.01985', '-0.01477', '0.0154', '0.02278', '0.006405', '0.0699', '0.06866', '-0.06354', '0.0699', '-0.0346', '0.005386', '0.01289', '-0.03287', '0.01828', '0.03069', '0.01874', '-0.003117', '-0.04285', '-0.03845', '-0.01251', '-0.003609', '0.00394', '0.0705', '-0.01517', '0.00922', '0.02843', '0.0266', '0.0652', '0.00761', '0.02525', '0.0639', '-0.01617', '0.01316', '0.1328', '0.04846', '0.06683', '-0.08545', '-0.02686', '0.02461']",,,C563661,,,,
mondo:0012562,holoprosencephaly 7,"['PTCH1 holoprosencephaly', 'holoprosencephaly 7', 'holoprosencephaly type 7', 'HPE7', 'holoprosencephaly caused by mutation in PTCH1']",0110876,610828,,C1835820,,,,C563660,,,,
mondo:0012563,holoprosencephaly 9,"['holoprosencephaly with microphthalmia and first branchial arch anomalies', 'holoprosencephaly type 9', 'GLI2 holoprosencephaly', 'holoprosencephaly caused by mutation in GLI2', 'HPE9', 'holoprosencephaly with microphthalmia and first branchial Arch anomalies', 'holoprosencephaly 9', 'pituitary anomalies with holoprosencephaly-like features']",0110873,610829,,C1835819,,,,,,,,
mondo:0012564,Polyosteolysis-hyperostosis syndrome,"['Polyosteolysis/hyperostosis syndrome', 'Polyosteolysis-hyperostosis syndrome']",,610830,,C1835818,,,,C563658,,,,
mondo:0012565,Fanconi anemia complementation group N,"['Fanconi anemia complementation group type N', 'Fanconi Anemia, complementation group type N', 'PALB2 Fanconi anaemia', 'Fanconi anemia caused by mutation in PALB2', 'PALB2 Fanconi anemia', 'Fanconi anemia, complementation group N', 'Fanconi anaemia caused by mutation in PALB2', 'Fanconi anaemia complementation group type N', 'FANCN']",0111094,610832,,C1835817,,,,C563657,,,,
mondo:0012566,"autism, susceptibility to, 11","['AUTS11', 'autism susceptibility 11', 'autism, susceptibility to, 11']",,610836,,,,,,,,,,
mondo:0012567,"autism, susceptibility to, 12","['autism, susceptibility to, 12', 'AUTS12', 'autism susceptibility 12']",,610838,,,,,,,,,,
mondo:0012568,osteoarthritis susceptibility 4,"['osteoarthritis, generalized, without dysplasia', 'OS4', 'osteoarthritis susceptibility 4']",,610839,,C1835815,,,,,,,,
mondo:0012569,"mitral valve prolapse, myxomatous 3","['mitral valve prolapse, myxomatous 3', 'myxomatous mitral valve prolapse 3', 'MVP3', 'MMVP3', 'mitral valve prolapse 3']",,610840,,C1835814,,,,C563655,,,,
mondo:0012570,body skin hyperlaxity due to vitamin K-dependent coagulation factor deficiency,"['PXE-like syndrome', 'pseudoxanthoma elasticum-like syndrome', 'PXE-like disorder with multiple coagulation Factor deficiency', 'pseudoxanthoma elasticum-like disorder with multiple coagulation factor deficiency']",,610842,91135,C4049241,"['-0.0553', '0.3865', '-0.0608', '-0.0929', '0.3372', '0.06366', '-0.1797', '-0.349', '-0.1996', '-0.1709', '-0.2363', '0.05267', '-0.01325', '-0.154', '-0.00818', '0.06305', '0.2286', '-0.005764', '-0.738', '-0.5747', '0.337', '-0.459', '0.402', '-0.2876', '-0.326', '0.2233', '-0.2267', '-0.0186', '0.00339', '-0.3418', '0.567', '0.1293', '-0.009254', '0.2181', '0.1411', '-0.5103', '0.02953', '-0.2434', '0.138', '0.00718', '0.278', '-0.701', '-0.0407', '0.0812', '0.2063', '-0.5083', '0.3286', '0.165', '0.3503', '-0.02773', '-0.285', '-0.6396', '0.7056', '0.6694', '-0.777', '-0.4229', '0.1769', '-0.1409', '-0.2115', '-0.05447', '-0.05957', '-0.2883', '0.1775', '-0.2825', '0.2822', '0.02495', '-0.0749', '0.2244', '-0.581', '0.3896', '-0.562', '-0.2905', '-0.2756', '-0.1174', '-0.0141', '0.257', '-0.0285', '0.1755', '0.4138', '-0.3582', '-0.07733', '0.3032', '0.1127', '0.433', '0.0245', '0.0673', '-0.3328', '0.4873', '0.491', '-0.1443', '0.482', '0.4248', '0.01288', '-0.3396', '0.3464', '0.365', '0.1357', '-0.485', '0.3342', '0.1967']",,,C563654,,,,
mondo:0012571,primary ciliary dyskinesia 6,"['NME8 primary ciliary dyskinesia', 'primary ciliary dyskinesia type 6', 'primary ciliary dyskinesia caused by mutation in NME8', 'ciliary dyskinesia, primary, type 6', 'ciliary dyskinesia, primary, 6', 'CILD6']",0110606,610852,,C1970506,,,,C567057,,,,
mondo:0012572,Sakoda complex,"['Sakoda complex', 'Sakoda spectrum', 'sphenoethmoidal encephalomeningocele, agenesis of the corpus callosum, and cleft Lip/palate', 'sphenoethmoidal encephalomeningocele agenesis of the corpus callosum and cleft lip/palate']",,610871,,C1970485,,,,C567055,,,,
mondo:0012573,vesicoureteral reflux 2,"['ROBO2 vesicoureteral reflux (disease)', 'VUR2', 'vesicoureteral reflux 2', 'vesicoureteral reflux type 2']",,610878,,C1970483,,,,C567053,,,,
mondo:0012574,Potocki-Lupski syndrome,"['Potocki-Lupski syndrome', '17p11.2 microduplication syndrome', 'PTLS', 'trisomy 17p11.2', 'chromosome 17P11.2 Duplication syndrome', 'Potocki-Lupski syndrome (dup(17)(p11.2p11.2))', '17p11.2 Duplication syndrome', 'Duplication 17p11.2 syndrome', 'Potocki-Lupski syndrome, Isolated cases', 'chromosome 17p11.2 duplication syndrome']",0060853,610883,1713,C2931246,,C124846,,,,,,
mondo:0012575,branchiootorenal syndrome 2,"['SIX5 branchio-oto-renal syndrome', 'branchiootorenal syndrome type 2', 'branchiootorenal syndrome 2', 'BOR2', 'branchio-oto-renal syndrome caused by mutation in SIX5']",0111424,610896,,C1970479,,,,,,,,
mondo:0012576,"supranuclear palsy, progressive, 3","['PSNP3', 'supranuclear palsy, progressive, 3']",,610898,,C1970476,,,,C567050,,,,
mondo:0012577,"asthma-related traits, susceptibility to, 4","['asthma-related traits, susceptibility to, 4', 'asthma-related traits, susceptibility to, type 4', 'asthma and allergic rhinitis, susceptibility to', 'ASRT4']",,610906,,,,,,,,,,
mondo:0012578,"autism, susceptibility to, 13","['autism susceptibility 13', 'AUTS13', 'autism, susceptibility to, 13']",,610908,,,,,,,,,,
mondo:0012579,autoimmune pulmonary alveolar proteinosis,"['pulmonary alveolar proteinosis, acquired', 'APAP', 'iPAP', 'acquired pulmonary alveolar proteinosis', 'pulmonary alveolar lipoproteinosis, acquired', 'Pap, acquired', 'idiopathic PAP', 'pulmonary alveolar lipoproteinosis acquired', 'autoimmune PAP', 'PAP', 'pulmonary alveolar proteinosis, autoimmune', 'PAP acquired', 'pulmonary alveolar proteinosis acquired', 'idiopathic pulmonary alveolar proteinosis', 'pulmonary alveolar proteinosis autoimmune']",,610910,747,C1970472,,,,C567049,,,,
mondo:0012580,hereditary pulmonary alveolar proteinosis,"['sufactant metabolism dysfunction, pulmonary', 'inborn error of pulmonary surfactant metabolism', 'congenital pulmonary alveolar proteinosis', 'pulmonary alveolar proteinosis, congenital', 'congenital PAP', 'hereditary pulmonary alveolar proteinosis']",,,264675,C2931035,"['-0.625', '0.0377', '-0.586', '0.0854', '0.1329', '-0.62', '0.2554', '0.4333', '0.1321', '-0.005417', '0.08765', '0.1832', '-0.373', '0.149', '-0.0974', '0.0276', '-0.3044', '0.0701', '0.0297', '-0.4814', '0.1532', '-0.4626', '0.497', '-0.1351', '0.2595', '0.2974', '0.1792', '0.3623', '-0.4011', '-0.1235', '0.838', '-0.001997', '0.5293', '-0.2532', '-0.0569', '-0.8496', '-0.587', '0.11194', '-0.1013', '-0.0875', '-0.1362', '0.4988', '0.1722', '0.2303', '-0.3298', '0.304', '-0.3298', '-0.4443', '-0.118', '0.7334', '-0.04666', '-0.2327', '-0.4604', '0.1897', '-0.4016', '-0.3276', '0.04395', '-0.3093', '-0.1885', '-0.014', '-0.2428', '0.626', '-0.3193', '-0.2585', '0.1373', '-0.893', '0.7236', '0.1992', '-0.4456', '0.283', '-0.2045', '-0.3447', '0.08356', '0.4268', '0.7285', '-0.03253', '0.6875', '-0.2656', '-0.05704', '-0.2167', '-0.5728', '-0.0419', '0.2822', '-0.0866', '-0.005688', '0.277', '0.2341', '0.864', '-0.06204', '0.05807', '-0.03867', '0.8223', '-1.077', '-0.0498', '0.9604', '0.458', '0.7173', '-0.2766', '-0.54', '-0.3723']",,,C535832,,,,
mondo:0012581,osteogenesis imperfecta type 8,"['osteogenesis imperfecta caused by mutation in P3H1', 'osteogenesis imperfecta type VIII', 'osteogenesis imperfecta, type 8', 'OI type VIII', 'osteogenesis imperfecta, type VIII', 'OI8', 'P3H1 osteogenesis imperfecta', 'OI, type 8']",0110336,610915,216812,,,,,C536049,,,,
mondo:0012582,interstitial lung disease due to ABCA3 deficiency,"['surfactant metabolism dysfunction, pulmonary, 3', 'pulmonary alveolar proteinosis, congenital, 3', 'interstitial lung disease due to ABCA3 deficiency', 'SMDP3', 'surfactant metabolism dysfunction, pulmonary, type 3', 'interstitial lung disease due to ATP-binding cassette subfamily A member 3 deficiency']",,610921,440402,C1970456,,,,C567046,,,,
mondo:0012583,"tooth agenesis, selective, 5","['STHAG5', 'he-Zhao deficiency', 'tooth agenesis, selective, 5', 'hypodontia/oligodontia 5']",,610926,,C1858210,,,,C565757,,,,
mondo:0012584,"systemic lupus erythematosus, susceptibility to, 9","['susceptibility to systemic lupus erythematosus 9', 'systemic lupus erythematosus, susceptibility to, type 9', 'systemic lupus erythematosus, susceptibility to, 9', 'SLEB9', 'CR2 systemic lupus erythematosus (disease)']",,610927,,,,,,,,,,
mondo:0012585,"coronary heart disease, susceptibility to, 7","['coronary heart disease, susceptibility to, 7', 'susceptibility to coronary heart disease 7', 'coronary heart disease, susceptibility to, type 7', 'coronary artery disease caused by mutation in CD36', 'CHDS7', 'CD36 coronary artery disease']",,610938,,,,,,,,,,
mondo:0012586,"coronary artery disease, autosomal dominant 2","['coronary artery disease, autosomal dominant, 2', 'LRP6 coronary artery disease', 'coronary artery disease, autosomal dominant type 2', 'ADCAD2', 'coronary artery disease caused by mutation in LRP6', 'coronary artery disease, autosomal dominant 2']",,610947,,C1970440,"['-0.02246', '0.0786', '0.00902', '-0.01476', '0.06226', '-0.1565', '0.0569', '0.11285', '-0.06805', '-0.0706', '-0.05328', '-0.08154', '0.02568', '0.01468', '-0.01886', '-0.09064', '-0.02411', '0.00258', '-0.05142', '-0.1781', '-0.0274', '-0.04703', '0.0741', '-0.02861', '0.02773', '-0.02007', '-0.004833', '-0.00475', '0.0762', '-0.0652', '0.1415', '0.009415', '0.11237', '0.01787', '0.005993', '-0.05392', '0.01048', '-0.01157', '0.067', '-0.1512', '0.0398', '-0.05438', '0.11487', '0.0256', '0.003849', '-0.10504', '-0.00525', '0.08344', '0.012886', '0.005295', '0.02643', '-0.01515', '0.0458', '-0.004387', '-0.02904', '-0.10364', '0.1014', '-0.03122', '-0.1247', '-0.04263', '0.05374', '0.06042', '0.01823', '-0.02971', '0.04745', '0.00886', '0.0839', '0.0999', '-0.1133', '0.1373', '-0.09607', '-0.03314', '0.02191', '-0.0997', '0.07153', '0.0851', '-0.00478', '0.0131', '-0.1311', '-0.0788', '-0.07776', '-0.02763', '-0.011246', '0.0775', '-0.00428', '0.04398', '0.10626', '0.1259', '0.1156', '0.04953', '0.04358', '0.0905', '0.06934', '0.04352', '0.2712', '0.0831', '0.1009', '-0.1233', '-0.07996', '0.01694']",,,C567045,,,,
mondo:0012587,"hypertension, essential, susceptibility to, 7","['hypertension, essential, susceptibility to, type 7', 'Hyt7', 'hypertension, essential, susceptibility to, 7']",,610948,,,,,,,,,,
mondo:0012588,neuronal ceroid lipofuscinosis 7,"['ceroid lipofuscinosis, neuronal, 7', 'CLN7 disease, late infantile', 'ceroid lipofuscinosis, neuronal, type 7', 'CLN7 disease', 'CLN7', 'neuronal ceroid lipofuscinosis type 7', 'neuronal ceroid lipofuscinosis caused by mutation in MFSD8', 'MFSD8 neuronal ceroid lipofuscinosis']",0110722,610951,228366,,"['0.1013', '0.711', '-0.1688', '-0.02498', '0.246', '-1.11', '-0.04593', '0.3567', '-0.1737', '0.010864', '-0.6665', '-0.03687', '-0.04565', '0.0112', '0.3909', '-0.4497', '-0.1904', '-0.559', '0.1218', '-0.2654', '0.1437', '-0.4263', '-0.2224', '-0.2324', '0.09753', '-0.4287', '-0.4456', '-0.26', '-0.795', '0.4175', '1.097', '-0.2312', '0.5024', '-0.3296', '0.6343', '0.11633', '-0.8433', '0.4595', '-0.3074', '0.005882', '-0.2346', '-0.3264', '1.048', '-0.0927', '0.3271', '-0.8184', '-0.1823', '0.01032', '0.2489', '0.214', '0.7163', '0.405', '-0.928', '-0.1503', '0.5864', '-1.246', '0.727', '-0.2468', '-0.6416', '0.0826', '0.2494', '0.12335', '0.362', '-0.0319', '0.305', '-0.10834', '0.799', '-0.09247', '-0.3403', '0.3818', '-0.1716', '0.2236', '-0.2607', '-0.768', '0.4478', '0.3423', '0.067', '0.1088', '-0.8306', '-0.0753', '0.882', '0.2898', '-0.5005', '0.2031', '0.4702', '-0.391', '0.277', '0.9185', '-0.07324', '0.5244', '-0.1451', '0.3647', '-0.5923', '-0.03775', '0.336', '0.05408', '0.711', '-0.1958', '0.7256', '-0.2676']",,,C563989,,,,
mondo:0012589,Pitt-Hopkins syndrome,"['encephalopathy, Severe epileptic, with autonomic dysfunction', 'intellectual disability, Syndromal, with intermittent hyperventilation', 'intellectual disability, wide mouth, distinctive facial features, and intermittent hyperventilation followed by apnea', 'Pitt Hopkins syndrome', 'mental retardation, Syndromal, with intermittent hyperventilation', 'PTHS', 'Pitt-Hopkins syndrome']",0060488,610954,2896,C1970431,"['0.4531', '-0.0003285', '-0.2236', '-0.2274', '0.1399', '0.1742', '0.1288', '0.7754', '-0.918', '-0.2585', '-0.3386', '0.0599', '0.4775', '-0.343', '0.1119', '-0.1012', '0.3489', '-0.0615', '-0.6426', '-0.71', '-0.552', '0.722', '0.4014', '-0.1517', '0.471', '-0.2627', '-0.3833', '-0.1581', '0.3801', '-0.3748', '0.2717', '-0.66', '0.415', '-0.588', '0.1918', '-0.4165', '0.1318', '-0.4355', '-0.1156', '0.0787', '0.6895', '0.363', '-0.12445', '-0.11127', '0.2488', '-0.286', '-0.2493', '0.1306', '0.04214', '0.388', '-0.4375', '-0.1599', '-0.2134', '-0.494', '0.0736', '-0.02608', '0.4075', '0.7227', '-0.2612', '0.11145', '0.133', '0.643', '0.1508', '0.3953', '0.1176', '-0.01662', '0.1257', '0.006557', '-0.2062', '0.7524', '-0.0998', '0.2267', '0.04926', '0.1451', '-0.2822', '-0.02301', '0.4006', '-0.2047', '-0.725', '0.11536', '0.4138', '-0.5874', '0.2369', '0.613', '0.6035', '0.1146', '-0.483', '0.2546', '-0.0831', '0.1599', '-0.415', '0.2', '-0.2484', '0.06155', '0.0942', '0.07324', '-0.02629', '-0.7197', '0.5103', '0.3213']",C129872,,C537403,758.5,,,
mondo:0012590,XFE progeroid syndrome,"['XPF-ERCC1 progeroid syndrome', 'XFEPS', 'XFE progeroid syndrome']",0060590,610965,,C1970416,"['-0.03275', '0.0315', '0.018', '-0.004326', '0.00818', '-0.05322', '0.00912', '0.05484', '-0.038', '-0.0094', '-0.00954', '0.00792', '-0.001296', '0.007687', '-0.02637', '-0.01375', '0.003082', '0.002779', '-0.01689', '-0.072', '-0.002167', '0.002468', '0.03812', '-0.00399', '0.01938', '-0.006363', '-0.02005', '-0.0129', '0.007427', '-0.01851', '0.03745', '-0.003023', '0.0551', '0.01619', '0.01956', '-0.0145', '0.002335', '-0.01913', '-0.01608', '-0.04816', '0.01993', '-0.02997', '0.000207', '-0.02011', '0.01281', '-0.0501', '-0.01017', '0.02711', '0.00599', '0.006626', '-0.0282', '0.01516', '0.02176', '0.01214', '-0.02135', '-0.01585', '0.011604', '-0.011894', '-0.03973', '0.001755', '0.02298', '0.003136', '-0.005207', '-0.005287', '0.008736', '0.01273', '0.03177', '0.01959', '-0.02278', '0.0649', '-0.03247', '0.0001653', '0.02066', '-0.01836', '0.005856', '-0.003336', '0.00456', '-0.02664', '-0.03473', '-0.02051', '0.002144', '-0.00414', '-0.02853', '0.0415', '0.006336', '-0.002708', '0.0279', '0.03992', '0.05447', '0.02267', '0.01982', '0.02998', '-0.004112', '0.02374', '0.0633', '0.01317', '0.03348', '-0.05637', '-0.004494', '0.00662']",C173111,,C567043,,,,
mondo:0012591,osteogenesis imperfecta type 5,"['IFITM5 osteogenesis imperfecta', 'osteogenesis imperfecta, type 5', 'OI5', 'OI, type 5', 'OI type 5', 'OI type V', 'OI with calcification in interosseous membranes', 'osteogenesis imperfecta, type V', 'osteogenesis imperfecta type V', 'type V OI', 'osteogenesis imperfecta caused by mutation in IFITM5']",0110344,610967,216828,C1970414,"['-0.3884', '-0.1198', '0.0182', '-0.3645', '0.6465', '-0.1954', '-0.143', '0.7134', '-0.3677', '0.1033', '-0.08936', '0.3425', '0.1948', '-0.1448', '-0.02141', '-0.03638', '0.813', '-0.04617', '0.1633', '-0.4333', '0.1388', '0.0354', '0.7886', '-0.1077', '-0.1705', '0.4636', '0.000987', '0.01581', '-0.3662', '0.1927', '-0.1998', '-0.04227', '0.062', '0.3733', '-0.3066', '0.1086', '-0.4988', '-0.338', '-0.2888', '-0.685', '-0.1235', '-0.2275', '0.1251', '-0.2313', '-0.4912', '-0.956', '0.2615', '0.506', '0.789', '-0.11725', '0.4824', '-0.7646', '0.3767', '-0.3096', '-0.00999', '-0.5117', '-0.2441', '-0.1744', '-0.1736', '-0.184', '-0.04947', '-0.10205', '-0.08234', '-0.3074', '-0.3477', '0.1324', '-0.06586', '0.7656', '-0.59', '0.321', '0.11615', '-0.2108', '0.1064', '-0.5693', '0.2583', '0.02895', '-0.2325', '0.3657', '0.2844', '-0.3552', '-0.3245', '-0.2825', '-0.1749', '0.2478', '-0.4558', '0.4263', '0.2382', '0.3733', '0.675', '-0.242', '-0.03958', '0.3164', '0.1348', '0.283', '0.5737', '0.401', '0.4075', '-0.585', '0.48', '-0.1875']",,,C567042,,,,
mondo:0012592,osteogenesis imperfecta type 11,"['OI type XI', 'osteogenesis imperfecta, type XI', 'osteogenesis imperfecta type XI', 'FKBP10 osteogenesis imperfecta', 'osteogenesis imperfecta caused by mutation in FKBP10', 'OI type 11', 'OI11', 'OI, type 11', 'osteogenesis imperfecta, type 11']",0110351,610968,216820,C3151218,,,,,,,,
mondo:0012593,brain-lung-thyroid syndrome,"['brain-lung-thyroid syndrome', 'choreoathetosis and congenital hypothyroidism with or without pulmonary dysfunction', 'choreoathetosis-hypothyroidism-neonatal respiratory distress', 'BLT syndrome', 'choreoathetosis-hypothyroidism-neonatal respiratory distress syndrome', 'CAHTP', 'choreoathetosis, hypothyroidism, and neonatal respiratory distress']",,610978,209905,,"['0.2181', '0.7344', '-0.598', '0.2003', '0.1348', '-0.408', '0.2659', '0.4897', '-0.6616', '-0.0502', '-0.189', '0.1615', '0.1608', '0.2301', '0.703', '-0.404', '0.3342', '-0.2603', '-0.2069', '-0.752', '0.0933', '0.1405', '1.035', '-0.879', '0.4033', '0.2683', '-0.1086', '0.6274', '0.7197', '-0.6196', '-0.02754', '0.2908', '0.4006', '-0.10504', '-0.4346', '-0.7505', '-0.5703', '-0.283', '0.154', '0.9326', '0.293', '-0.1759', '0.469', '-0.0705', '0.48', '0.159', '0.373', '-0.2167', '0.0751', '0.1243', '-0.2793', '0.434', '-0.5894', '-0.08594', '-0.7275', '-0.1222', '0.4597', '0.0834', '0.06696', '0.4138', '0.3733', '-0.00642', '0.277', '-0.0811', '0.03592', '0.09467', '0.673', '0.01038', '-0.8823', '-0.2776', '0.0995', '-0.0741', '0.713', '-0.2253', '0.3796', '-0.1761', '0.322', '-0.683', '-0.2625', '0.2942', '-0.4138', '-0.11505', '-0.2505', '0.312', '-0.00349', '0.04187', '0.2986', '0.6875', '0.482', '0.06226', '0.4495', '0.1979', '-0.282', '-0.2627', '0.727', '0.0864', '0.2976', '-0.363', '0.4146', '0.1737']",,,C567034,,,,
mondo:0012594,complement factor I deficiency,"['complement Factor 1 deficiency', 'complement component 3 inactivator deficiency', 'complement factor I deficiency', 'C3 inactivator deficiency', 'CFID', 'immunodeficiency with factor I anomaly']",0050419,610984,200418,C3463916,"['-0.131', '0.0782', '-0.1287', '-0.446', '-0.04385', '0.114', '0.2166', '-0.2603', '0.04318', '0.2355', '0.01591', '0.2198', '-0.000594', '-0.10095', '-0.1484', '-0.341', '-0.0005593', '0.2107', '-0.0831', '-0.5576', '0.08105', '-0.504', '0.7373', '-0.1427', '0.2795', '0.1875', '-0.10956', '0.02306', '-0.1266', '-0.3406', '0.2399', '0.3013', '0.6064', '0.2467', '-0.0938', '-0.1948', '-0.387', '0.04153', '-0.1609', '-0.651', '-0.413', '0.3174', '0.00992', '-0.2161', '-0.04977', '-0.292', '-0.0978', '0.1907', '-0.0636', '0.6147', '-0.1126', '-0.04898', '0.4944', '-0.3254', '-0.4204', '0.124', '0.05533', '-0.546', '-0.5254', '0.191', '0.072', '0.3628', '0.03044', '0.04037', '0.274', '0.1213', '0.413', '0.1926', '-0.3306', '0.3281', '-0.4463', '-0.1833', '-0.165', '-0.2467', '0.1963', '-0.4546', '0.5854', '0.1692', '0.352', '0.112', '-0.2913', '-0.3364', '0.1821', '0.322', '-0.3667', '-0.07635', '0.1444', '0.527', '0.3088', '-0.2798', '0.5127', '0.537', '0.0285', '-0.01094', '0.6987', '0.8984', '0.338', '-0.2527', '-0.4783', '0.232']",,,C572568,,,,
mondo:0012595,"leprosy, susceptibility to, 4","['leprosy, susceptibility to, type 4', 'LTA leprosy', 'leprosy, early-onset, susceptibility to', 'leprosy, susceptibility to, 4', 'leprosy caused by mutation in LTA', 'susceptibility to leprosy 4', 'LPRS4']",,610988,,,,,,,,,,
mondo:0012596,PSAT deficiency,"['PSATD', 'phosphoserine aminotransferase deficiency', 'PSAT deficiency']",0050723,610992,284417,C1970253,"['-0.434', '0.3323', '0.1682', '-0.2961', '-0.03876', '-0.4087', '-0.1483', '0.3933', '-0.1615', '-0.1044', '-0.2732', '-0.1174', '-0.1139', '-0.3862', '0.01187', '0.0433', '0.26', '-0.0004177', '-0.326', '-0.8555', '0.00532', '-0.284', '0.2438', '-0.574', '0.267', '0.07135', '-0.129', '-0.1985', '0.03162', '-0.4727', '0.08795', '0.2482', '0.5', '0.3794', '-0.3896', '0.07733', '-0.0951', '-0.1804', '-0.2617', '-0.004482', '0.01022', '-0.6187', '0.01775', '-0.4285', '-0.102', '-0.0803', '0.1082', '0.1915', '-0.2593', '0.1989', '-0.0319', '-0.1409', '-0.3542', '0.0958', '-0.3843', '-0.3623', '0.1431', '-0.1959', '-0.4785', '0.494', '0.1799', '-0.1495', '0.2861', '-0.1661', '-0.0552', '-0.2656', '0.2034', '-0.0974', '-0.717', '-0.0825', '-0.4263', '0.4177', '0.12463', '-0.2822', '0.01778', '0.2043', '0.2394', '-0.321', '-0.4514', '0.1462', '0.4897', '0.3113', '-0.1592', '0.09344', '0.6704', '0.03653', '0.1803', '0.3318', '0.587', '0.2019', '0.592', '0.7627', '0.03098', '0.05872', '0.6577', '0.796', '0.2222', '-0.626', '0.4646', '-0.1755']",,,C567032,,,,
mondo:0012597,"prostate cancer, hereditary, 9","['HPC9', 'prostate cancer, hereditary, 9', 'prostate cancer, hereditary, type 9']",,610997,,C1970250,,,,C567031,,,,
mondo:0012598,"fibromatosis, gingival, 4","['gingival fibromatosis, 4', 'GGF4', 'HGF4', 'hereditary gingival fibromatosis, 4', 'fibromatosis gingival, hereditary, 4', 'fibromatosis, gingival, hereditary, 4', 'fibromatosis, gingival, 4', 'GINGF4']",,611010,,,,,,C567028,,,,
mondo:0012599,"hypertension, essential, susceptibility to, 8","['hypertension, essential, susceptibility to, 8', 'HYT8']",,611014,,,,,,,,,,
mondo:0012600,"autism, susceptibility to, 9","['autism, susceptibility to, 9', 'AUTS9']",,611015,,,,,,,,,,
mondo:0012601,"autism, susceptibility to, 10","['autism, susceptibility to, 10', 'AUTS10']",,611016,,,,,,,,,,
mondo:0012602,autosomal recessive nonsyndromic hearing loss 24,"['DFNB24', 'RDX autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive 24', 'autosomal recessive nonsyndromic deafness type 24', 'autosomal recessive nonsyndromic deafness caused by mutation in RDX', 'autosomal recessive nonsyndromic deafness 24', 'autosomal recessive deafness 24', 'deafness, autosomal recessive type 24']",0110482,611022,,C1970239,,,,C567027,,,,
mondo:0012603,episodic kinesigenic dyskinesia 2,"['dystonia 19', 'episodic kinesigenic dyskinesia 2', 'episodic kinesigenic dyskinesia type 2', 'EKD2']",0090054,611031,98809,C1970238,"['-0.0869', '0.2139', '-0.091', '-0.1032', '0.0812', '-0.4055', '0.1984', '0.0675', '-0.1172', '-0.0835', '-0.11084', '0.02388', '0.01514', '-0.0989', '0.2512', '0.1814', '-0.03598', '-0.2286', '0.0531', '-0.4683', '0.0918', '0.06177', '-0.0743', '-0.1943', '-0.02092', '-0.03152', '-0.1843', '-0.142', '-0.1431', '-0.1002', '0.132', '0.2152', '0.03824', '-0.125', '-0.00792', '0.0601', '0.04156', '-0.186', '-0.1016', '-0.2307', '0.2408', '-0.372', '-0.0308', '0.004734', '0.12366', '-0.2118', '-0.1742', '0.1328', '0.2048', '0.338', '-0.3027', '-0.03864', '-0.0486', '0.07654', '0.1469', '-0.3574', '0.3467', '-0.09607', '-0.009605', '-0.0395', '-0.003925', '0.1033', '0.197', '-0.1232', '-0.2537', '0.1338', '0.3516', '0.2695', '-0.1954', '0.2406', '-0.188', '0.025', '0.005737', '-0.09814', '0.1236', '0.1542', '0.1134', '0.1897', '-0.08325', '-0.05563', '0.1306', '0.0471', '0.10504', '0.06445', '-0.0284', '-0.10925', '0.1177', '0.333', '0.1252', '0.2517', '-0.1131', '0.1876', '0.102', '0.1733', '0.4922', '0.139', '0.2091', '-0.1305', '-0.02672', '0.03232']",,,C567026,,,,
mondo:0012604,isolated microphthalmia 3,"['microphthalmia, isolated type 3', 'isolated microphthalmia caused by mutation in rax', 'isolated microphthalmia type 3', 'RAX isolated microphthalmia', 'rax isolated microphthalmia', 'microphthalmia, isolated 3', 'MCOP3']",0060842,611038,,C1970237,,,,C567025,,,,
mondo:0012605,isolated microphthalmia 5,"['MCOP5', 'microphthalmia-retinitis pigmentosa-foveoschisis-optic disk drusen syndrome', 'microphthalmia-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome', 'microphthalmia, isolated type 5', 'isolated microphthalmia caused by mutation in MFRP', 'posterior microphthalmia with retinitis pigmentosa, foveoschisis and optic disc drusen', 'microphthalmia, isolated 5', 'microphthalmia, posterior, with retinitis pigmentosa, foveoschisis, and optic Disc drusen', 'isolated microphthalmia type 5', 'Nanophtalmos-retinitis pigmentosa-foveoschisis-optic disc drusen syndrome', 'MFRP isolated microphthalmia', 'posterior microphthalmia with retinitis pigmentosa, foveoschisis and optic disk drusen', 'Nanophtalmos-retinitis pigmentosa-foveoschisis-optic disk drusen syndrome']",0060837,611040,251279,C1970236,"['-0.5283', '0.03583', '-0.1439', '-0.012886', '-0.01208', '-0.3452', '-0.0827', '0.161', '-0.4468', '-0.2386', '-0.1866', '-0.2603', '-0.3196', '-0.2228', '-0.0743', '-0.4119', '0.305', '-0.09796', '0.206', '-0.6973', '-0.10565', '-0.12177', '-0.09973', '0.0969', '0.1525', '0.3174', '-0.3352', '0.1954', '-0.02454', '0.2141', '0.2532', '0.1675', '0.2617', '0.379', '0.2244', '-0.05902', '0.1527', '-0.3755', '0.1033', '-0.5034', '0.1414', '-0.06744', '0.03537', '-0.1781', '-0.2195', '-0.02112', '0.0696', '0.1023', '0.1766', '-0.1812', '0.1525', '0.1875', '0.01814', '-0.3484', '-0.07526', '-0.1617', '0.772', '0.1344', '-0.4888', '0.1923', '0.1121', '0.0847', '0.3484', '0.04776', '-0.3154', '0.0841', '0.4778', '0.591', '-0.1776', '0.2244', '-0.395', '0.01558', '0.1226', '-0.1655', '0.1658', '-0.4966', '0.1766', '-0.10223', '-0.1333', '-0.06384', '0.02888', '0.0403', '-0.0633', '0.647', '-0.1755', '-0.442', '0.04498', '0.3054', '0.08844', '0.292', '0.1738', '0.1903', '0.3054', '-0.01351', '0.6743', '-0.2769', '0.503', '-0.1731', '-0.08716', '0.1772']",,,C567024,,,,
mondo:0012606,"mycobacterium tuberculosis, susceptibility to, 2","['MTBS2', 'Mycobacterium tuberculosis, susceptibility to, type 2', 'mycobacterium tuberculosis, susceptibility to, 2']",,611046,,,,,,,,,,
mondo:0012607,"asthma-related traits, susceptibility to, 5","['asthma susceptibility 5', 'asthma-related traits, susceptibility to, type 5', 'inherited susceptibility to asthma caused by mutation in IRAK3', 'IRAK3 inherited susceptibility to asthma', 'asthma-related traits, susceptibility to, 5', 'ASRT5']",,611064,,,,,,,,,,
mondo:0012608,autosomal recessive lower motor neuron disease with childhood onset,"['distal spinal muscular atrophy type 4', 'spinal muscular atrophy, distal, autosomal recessive, 4', 'autosomal recessive distal spinal muscular atrophy type 4', 'spinal muscular atrophy, distal, autosomal recessive, type 4', 'DSMA4', 'dSMA4']",0111213,611067,206580,C1970211,"['-0.588', '-0.1882', '0.02501', '-0.3474', '-0.4639', '-0.7036', '0.1962', '1.245', '-0.899', '-0.3298', '-0.1313', '0.0112', '-0.3374', '0.1958', '0.8086', '-0.0008836', '0.1859', '-0.101', '-0.547', '-0.5674', '0.5435', '0.1971', '0.5825', '0.2368', '0.168', '-0.1407', '0.1575', '-0.3289', '-0.8657', '0.02028', '0.2502', '0.2937', '0.1283', '0.2158', '-0.4587', '-0.2935', '-0.2238', '0.03555', '-0.2988', '-0.233', '-0.324', '-0.05704', '-0.09265', '0.5938', '-0.3342', '-0.305', '-0.602', '0.04733', '-0.2957', '0.6025', '0.3066', '0.3508', '0.2083', '-0.3206', '-0.1626', '-0.6875', '0.3535', '0.178', '-0.1772', '0.08905', '-0.0851', '-0.1688', '0.0886', '0.3555', '-0.229', '0.3347', '0.2607', '0.4976', '-0.02383', '0.536', '-0.4785', '0.07477', '0.406', '-0.0903', '0.4968', '0.0654', '-0.1633', '0.6064', '-0.397', '-0.416', '-0.1329', '0.01129', '0.629', '0.5815', '-0.06216', '0.462', '0.02693', '-0.06335', '0.4434', '0.0184', '0.10895', '0.3186', '-0.01938', '0.6284', '0.2224', '0.7173', '0.5483', '-0.262', '0.01933', '0.5923']",,,C567023,,,,
mondo:0012609,Alzheimer disease 12,"['Alzheimer disease 12', 'Alzheimer disease familial 12', 'AD12', 'Alzheimer disease type 12', 'Alzheimer^s disease 12', 'Alzheimer disease, familial, 12', 'Ad12', 'Alzheimer^s disease type 12']",0110045,611073,,C1970209,,,,C567022,,,,
mondo:0012610,inflammatory bowel disease 10,"['inflammatory bowel disease type 10', 'ATG16L1 inflammatory bowel disease', 'IBD10', 'inflammatory bowel disease caused by mutation in ATG16L1', 'inflammatory bowel disease (Crohn disease) 10', 'inflammatory bowel disease 10']",0110885,611081,,C1970207,,,,C567021,,,,
mondo:0012611,"polyhydramnios, megalencephaly, and symptomatic epilepsy","['polyhydramnios, megalencephaly, and symptomatic epilepsy', 'polyhydramnios-megalencephaly-symptomatic epilepsy syndrome', 'polyhydramnios, megalencephaly, and symptomatic epilepsy syndrome', 'PMSE', 'PMSE syndrome', 'pretzel syndrome']",,611087,500533,C1970203,"['-0.0108', '0.05774', '0.0094', '-0.03867', '0.01058', '-0.07025', '0.012726', '0.0637', '-0.0709', '-0.0262', '-0.0433', '-0.00915', '-0.000718', '-0.00554', '-0.0007157', '-0.03238', '0.00774', '-0.02968', '-0.01072', '-0.09296', '0.006542', '-0.0376', '0.0446', '-0.01625', '0.02562', '-0.0352', '-0.015175', '0.0155', '-0.00188', '-0.02872', '0.0464', '0.001054', '0.06964', '0.02972', '0.00591', '-0.01785', '-0.00903', '-0.02026', '-0.01953', '-0.04688', '0.03543', '-0.0578', '0.0335', '-0.01633', '0.00667', '-0.042', '-0.02158', '0.03662', '-0.00971', '0.02144', '0.006947', '-0.001624', '0.01127', '-0.00397', '-0.012474', '-0.01718', '0.05484', '-0.03415', '-0.0494', '0.02588', '0.02376', '0.013535', '-0.00948', '0.00866', '-0.001108', '-0.002867', '0.0737', '0.0429', '-0.05643', '0.0627', '-0.03647', '0.01761', '0.00907', '-0.02066', '-0.00661', '0.01732', '0.03757', '-0.00862', '-0.03583', '-0.03494', '-0.0008245', '0.01008', '-0.02211', '0.06003', '-0.014366', '0.005974', '0.004253', '0.03912', '0.0663', '0.003824', '0.03708', '0.05026', '0.004566', '0.01326', '0.1024', '0.03934', '0.0719', '-0.07117', '0.0201', '0.01469']",,,C567020,,,,
mondo:0012612,"intellectual disability, autosomal recessive 12","['intellectual disability, autosomal recessive type 12', 'intellectual disability, autosomal recessive 12', 'mental retardation, autosomal recessive 12', 'mental retardation, autosomal recessive type 12', 'intellectual developmental disorder, autosomal recessive 12', 'MRT12']",0081180,611090,,C1970200,,,,C567019,,,,
mondo:0012613,"intellectual disability, autosomal recessive 5","['intellectual disability, autosomal recessive type 5', 'MRT5', 'mental retardation, autosomal recessive 5', 'mental retardation, autosomal recessive type 5', 'autosomal recessive non-syndromic intellectual disability caused by mutation in NSUN2', 'NSUN2 autosomal recessive non-syndromic intellectual disability', 'intellectual disability, autosomal recessive 5']",0081181,611091,,C1970199,,,,C567018,,,,
mondo:0012614,"intellectual disability, autosomal recessive 6","['mental retardation, autosomal recessive type 6', 'autosomal recessive non-syndromic intellectual disability caused by mutation in GRIK2', 'intellectual developmental disorder, autosomal recessive 6', 'GRIK2 autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive 6', 'MRT6', 'intellectual disability, autosomal recessive 6', 'intellectual disability, autosomal recessive type 6']",0081182,611092,,C1970198,,,,C567017,,,,
mondo:0012615,"intellectual disability, autosomal recessive 7","['intellectual disability, autosomal recessive 22', 'mental retardation, autosomal recessive 7', 'mental retardation, autosomal recessive type 7', 'intellectual disability, autosomal recessive type 7', 'MRT7', 'autosomal recessive non-syndromic intellectual disability caused by mutation in TUSC3', 'mental retardation, autosomal recessive 22', 'intellectual disability, autosomal recessive 7', 'TUSC3 autosomal recessive non-syndromic intellectual disability']",0081183,611093,,C1970197,,,,C567016,,,,
mondo:0012617,"intellectual disability, autosomal recessive 9","['mental retardation, autosomal recessive 9', 'MRT9', 'intellectual disability, autosomal recessive 26', 'mental retardation, autosomal recessive, 9/26', 'mental retardation, autosomal recessive 26', 'intellectual disability, autosomal recessive 9']",0081184,611095,,C1970195,,,,C567014,,,,
mondo:0012618,"intellectual disability, autosomal recessive 10","['mental retardation, autosomal recessive 10/20', 'mental retardation, autosomal recessive 20', 'mental retardation, autosomal recessive 10', 'MRT10', 'intellectual disability, autosomal recessive 20', 'intellectual disability, autosomal recessive 10']",0081185,611096,,C1970194,,,,C567013,,,,
mondo:0012619,"intellectual disability, autosomal recessive 11","['mental retardation, autosomal recessive, 11', 'mental retardation, autosomal recessive 11', 'intellectual disability, autosomal recessive 11', 'MRT11']",0081186,611097,,C1970193,,,,C567012,,,,
mondo:0012620,"prostate cancer, hereditary, 10","['prostate cancer, hereditary, 10', 'HPC10']",,611100,,C1970192,,,,C567011,,,,
mondo:0012621,deafness-infertility syndrome,"['deafness-infertility syndrome', 'chromosome 15Q15.3 deletion syndrome', 'deafness and male infertility', 'dis', 'deafness, sensorineural, and Male infertility', 'sensorineural deafness and male infertility']",,611102,94064,,"['0.2815', '-0.3206', '-0.2734', '-0.0722', '0.727', '-0.3965', '-0.2502', '0.9727', '-0.2169', '-0.3606', '0.06915', '0.2375', '-0.2073', '0.9785', '-0.02066', '-0.6187', '-0.2494', '0.6', '-0.5054', '-0.3928', '-0.05463', '-0.0506', '-0.458', '-0.6934', '0.1764', '-0.294', '-0.3074', '-0.2551', '0.005283', '-0.427', '0.7495', '-0.3184', '0.09', '0.132', '0.01392', '-0.3545', '-0.527', '-0.5044', '0.1992', '0.3357', '0.756', '0.3176', '0.5654', '-0.06854', '0.2766', '-0.4485', '-0.3406', '-0.00952', '0.74', '0.3035', '-0.287', '-0.1693', '0.1766', '0.4355', '-0.1831', '0.6523', '0.1461', '-0.23', '-0.3618', '-0.11884', '0.1602', '1.095', '0.201', '0.1897', '-0.5195', '0.4995', '-0.0441', '0.01836', '-0.7866', '0.763', '-0.3574', '-0.1809', '0.1114', '-0.41', '0.3635', '0.2292', '0.2468', '0.3674', '-0.329', '0.5215', '-0.3733', '0.1322', '0.2161', '-0.606', '-0.010895', '-0.2522', '0.1503', '-0.295', '0.525', '-0.442', '-0.3528', '0.06744', '-0.2505', '0.892', '0.3953', '-0.0154', '-0.04053', '-0.315', '-0.288', '-0.332']",,,C567010,758.39,,,
mondo:0012622,leukoencephalopathy with brain stem and spinal cord involvement-high lactate syndrome,"['leukoencephalopathy with brain stem and spinal cord involvement-lactate elevation syndrome', 'leukoencephalopathy with brain stem and spinal cord involvement and lactate elevation', 'leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation', 'LBSL', 'mitochondrial aspartyl-tRNA synthetase deficiency', 'leukoencephalopathy with brain stem and spinal cord involvement - lactate elevation', 'leukoencephalopathy with brain stem and spinal cord involvement - high lactate']",,611105,137898,,"['-0.03604', '0.1117', '-0.10126', '-0.4385', '-0.11615', '-0.3977', '-0.04388', '0.736', '-0.3523', '-0.2263', '-0.628', '-0.2484', '-0.3477', '-0.3494', '0.4202', '-0.22', '0.01859', '-0.165', '-0.3303', '-0.2421', '0.236', '-0.4805', '-0.1536', '-0.3547', '0.03445', '-0.0962', '-0.0566', '-0.05765', '-0.229', '-0.1853', '0.01616', '0.1556', '0.3625', '-0.05597', '0.2524', '-0.1292', '-0.2798', '-0.2394', '0.2969', '-0.0866', '0.005676', '-0.458', '0.06274', '0.003363', '-0.2598', '-0.12', '0.0643', '0.06366', '-0.3657', '-0.4353', '0.2222', '0.45', '-0.2054', '-0.11456', '-0.0976', '-0.00428', '0.4072', '-0.1654', '0.013985', '0.3506', '0.1058', '0.1521', '-0.007423', '-0.0418', '-0.517', '0.01513', '0.1755', '0.76', '-0.4634', '0.3027', '-0.0727', '0.558', '-0.2426', '0.02863', '0.07367', '0.02107', '0.216', '0.2067', '-0.09174', '0.0956', '-0.1777', '0.010704', '0.0301', '0.7104', '-0.0874', '0.018', '0.2142', '0.398', '0.369', '0.0528', '0.29', '0.3425', '0.04428', '0.1425', '0.67', '0.1951', '0.512', '-0.10767', '0.311', '0.04315']",,,C567009,,,,
mondo:0012623,"intellectual disability, autosomal recessive 4","['intellectual disability, autosomal recessive 4', 'mental retardation, autosomal recessive 4', 'mental retardation, autosomal recessive, 4', 'MRT4']",0081187,611107,,C1970179,,,,C567008,,,,
mondo:0012624,acyl-CoA dehydrogenase 9 deficiency,"['mitochondrial complex I deficiency due to ACAD9 deficiency', 'mitochondrial complex I deficiency, nuclear type 20', 'ACAD9 deficiency', 'acyl-CoA dehydrogenase 9 deficiency']",0112072,611126,99901,C1970173,"['-0.506', '0.3862', '-0.009796', '0.1302', '0.02426', '-0.5244', '0.2654', '0.08514', '-0.08344', '0.05246', '0.06775', '-0.1576', '-0.01752', '-0.0485', '-0.3364', '-0.629', '0.0972', '0.11127', '-0.5293', '-0.8433', '-0.05203', '-0.1377', '1.079', '-0.1381', '-0.259', '-0.04556', '0.104', '-0.06934', '-0.1533', '-0.28', '0.3252', '0.442', '0.3958', '0.02383', '-0.529', '-0.652', '-0.2236', '-0.164', '-0.3906', '-0.0808', '-0.1967', '-0.2656', '0.3455', '0.4417', '-0.1823', '-0.1333', '0.392', '-0.10254', '0.1621', '0.5347', '-0.2554', '-0.00458', '0.1384', '-0.00574', '-0.1566', '-0.545', '0.5747', '0.01126', '-0.2448', '0.2776', '0.4521', '0.0185', '0.493', '0.1272', '0.02748', '-0.034', '0.3474', '0.1127', '-0.918', '-0.06775', '-0.2124', '-0.0407', '0.3142', '0.1613', '0.1654', '0.4978', '0.2454', '-0.3572', '-0.04977', '0.4866', '0.344', '-0.09705', '-0.0905', '-0.1854', '0.5747', '0.3413', '0.1082', '0.0251', '0.96', '-0.3093', '0.2996', '0.305', '-0.5054', '0.17', '0.4468', '0.657', '0.2605', '0.0794', '0.02736', '0.227']",,,C567006,,,,
mondo:0012625,retinitis pigmentosa 37,"['NR2E3 retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in NR2E3', 'RP37', 'retinitis pigmentosa type 37', 'retinitis pigmentosa 37']",0110399,611131,,C1970163,,,,C567005,,H35.5,,
mondo:0012626,"Meckel syndrome, type 4","['MKS4', 'CEP290 Meckel syndrome', 'Meckel syndrome caused by mutation in CEP290', 'Meckel-Gruber syndrome, type 4', 'Meckel-like Cerebrorenodigital syndrome', 'Meckel syndrome, type 4', 'Meckel syndrome 4']",0070118,611134,,C1970161,,,,,,,,
mondo:0012627,"epilepsy, idiopathic generalized, susceptibility to, 13","['EIG13', 'epilepsy, juvenile myoclonic, susceptibility to, 5', 'epilepsy, idiopathic generalized, susceptibility to, 13', 'epilepsy, childhood absence, susceptibility to, 4', 'susceptibility to idiopathic generalized epilepsy 13', 'epilepsy, idiopathic generalized, susceptibility to, type 13', 'juvenile myoclonic epilepsy caused by mutation in GABRA1', 'susceptibility to idiopathic generalised epilepsy 13', 'GABRA1 juvenile myoclonic epilepsy']",0111314,611136,64280,,,,,C567002,,,,
mondo:0012628,"coronary heart disease, susceptibility to, 8","['CHDS8', 'coronary heart disease, susceptibility to, 8']",,611139,,,,,,,,,,
mondo:0012629,paroxysmal nonkinesigenic dyskinesia 2,"['PNKD2', 'dystonia 20', 'paroxysmal nonkinesigenic dyskinesia type 2', 'paroxysmal nonkinesigenic dyskinesia 2']",0090047,611147,,C1970149,,,,C567001,,,,
mondo:0012630,Alzheimer disease 13,"['AD13', 'Alzheimer^s disease type 13', 'Alzheimer disease 13', 'Alzheimer disease-13', 'Alzheimer^s disease 13']",0110046,611152,,C1970147,,,,C567000,,,,
mondo:0012631,Alzheimer disease 14,"['Alzheimer disease 14', 'Alzheimer disease-14', 'AD14', 'Alzheimer^s disease type 14', 'Alzheimer^s disease 14']",0110047,611154,,C1970144,,,,C566999,,,,
mondo:0012634,craniofacial dysplasia - osteopenia syndrome,"['HAMAMY syndrome', 'Hamamy syndrome', 'HMMS', 'hypertelorism, Severe, with midface prominence, myopia, intellectual disability, and bone fragility', 'hypertelorism, Severe, with midface prominence, myopia, mental retardation, and bone fragility']",,611174,314555,C1970027,"['-0.405', '-0.1749', '0.3687', '-0.341', '0.3035', '-0.569', '0.019', '0.767', '-0.7573', '0.3022', '-0.01091', '-0.2158', '0.09863', '-0.4602', '-0.1798', '-0.07135', '0.4797', '-0.1962', '-0.3245', '-0.2856', '0.4211', '0.03195', '0.2429', '-0.1364', '0.3584', '0.06226', '-0.3184', '0.07904', '0.2654', '-0.09', '0.05154', '-0.1877', '0.3801', '0.3523', '0.301', '-0.4583', '-0.1445', '-0.4614', '-0.2551', '-0.7837', '0.2983', '0.1797', '-0.1996', '-0.3323', '-0.446', '-0.3416', '0.09174', '0.506', '0.1143', '0.4336', '-0.3845', '-0.244', '0.1007', '0.2461', '-0.3213', '-0.4421', '-0.0783', '-0.1377', '0.10583', '0.1279', '0.1388', '0.1528', '-0.4243', '-0.08527', '-0.1114', '0.3154', '0.2029', '0.6514', '-0.2222', '0.481', '-0.0967', '0.1553', '0.02782', '0.02617', '-0.382', '-0.00631', '0.597', '-0.3044', '-0.06757', '0.08594', '0.1005', '-0.11365', '0.04666', '0.6714', '-0.2086', '-0.001607', '-0.4023', '0.5547', '0.4065', '0.716', '-0.1156', '0.4858', '0.1954', '0.3513', '0.472', '-0.11725', '0.543', '-0.619', '0.6064', '0.2822']",,,C566988,,,,
mondo:0012635,COG8-congenital disorder of glycosylation,"['COG8-CDG', 'CDG2H', 'carbohydrate deficient glycoprotein syndrome type IIh', 'congenital disorder of glycosylation type 2h', 'congenital disorder of glycosylation type IIh', 'CDG syndrome type IIh', 'COG8-CDG (CDG-IIh)', 'congenital disorder of glycosylation, type IIh', 'CDG-IIh', 'CDG IIh']",0070260,611182,95428,C1970021,"['-0.409', '0.1196', '0.145', '0.1577', '0.04044', '-0.578', '-0.6', '-0.03001', '-0.3828', '-0.2264', '-0.1768', '-0.2103', '0.03363', '-0.0592', '-0.1101', '0.3672', '-0.1123', '0.2294', '-0.5776', '-0.2233', '0.06934', '-0.001372', '0.05435', '-0.3342', '0.3225', '-0.1028', '-0.0831', '-0.4158', '0.3416', '-0.3628', '0.1896', '0.3325', '0.3171', '0.272', '0.3193', '-0.2908', '0.164', '-0.05505', '-0.3135', '0.3323', '-0.1727', '-0.683', '-0.09045', '-0.09296', '-0.3196', '-0.606', '0.0986', '-0.0692', '0.1836', '0.1382', '-0.3396', '-0.00994', '0.01187', '0.686', '-0.2546', '-0.63', '0.4092', '0.2109', '-0.3662', '0.4333', '0.195', '-0.112', '0.05307', '-0.272', '0.1906', '-0.5615', '0.2338', '0.3335', '-0.779', '-0.1499', '-0.327', '0.1451', '-0.02678', '0.2015', '0.2238', '0.5483', '-0.0709', '0.2238', '-0.1138', '0.861', '0.2192', '0.08', '-0.07263', '0.3228', '0.188', '-0.1354', '0.3718', '0.2935', '0.423', '-0.0293', '0.03069', '0.322', '-0.4229', '-0.1732', '0.647', '0.781', '0.2179', '-0.812', '0.1677', '-0.05618']",,,C566987,,,,
mondo:0012636,"restless legs syndrome, susceptibility to, 6","['RLS6', 'restless legs syndrome 6', 'periodic limb movements in sleep', 'restless legs syndrome, susceptibility to, 6']",,611185,,,,,,,,,,
mondo:0012637,COG1-congenital disorder of glycosylation,"['CDG syndrome type IIg', 'carbohydrate deficient glycoprotein syndrome type IIg', 'CDG IIg', 'congenital disorder of glycosylation type IIg', 'Cdgii/Cog1 Cerebrocostomandibular-like syndrome', 'CDG2G', 'CDG-IIg', 'COG1-CDG', 'congenital disorder of glycosylation type 2g', 'CDG 2G', 'COG1-CDG (CDG-IIg)', 'congenital disorder of glycosylation, type IIg']",0070259,611209,263508,,"['-0.486', '0.2969', '0.2104', '-0.2327', '0.1267', '-0.498', '-0.2255', '0.4758', '-0.447', '-0.4812', '-0.2341', '0.1852', '0.1372', '-0.06946', '-0.1688', '0.1433', '0.2732', '0.03023', '-0.441', '-0.65', '0.0727', '0.1743', '0.1819', '-0.5454', '0.0643', '0.04025', '-0.3225', '-0.246', '0.2703', '-0.2463', '0.1064', '0.2032', '0.5747', '0.10767', '-0.4263', '0.1876', '-0.5347', '-0.001905', '-0.2688', '0.07874', '0.2367', '-0.3225', '0.1772', '-0.5737', '0.1458', '-0.1914', '0.2009', '0.1324', '-0.1831', '-0.268', '-0.1338', '0.075', '-0.291', '-0.01119', '-0.086', '-0.5166', '-0.0836', '-0.202', '-0.2664', '0.4604', '0.1567', '-0.232', '0.158', '-0.1783', '-0.00971', '-0.0537', '0.2861', '0.27', '-0.6704', '0.2605', '-0.4888', '0.315', '0.1345', '0.005005', '0.1735', '0.3328', '0.1084', '-0.2747', '-0.3757', '0.3123', '0.228', '-0.04645', '-0.3086', '0.2338', '0.3435', '0.2788', '0.2115', '0.2097', '0.443', '0.05624', '0.4849', '0.674', '-0.006424', '0.3381', '0.666', '0.5547', '0.1335', '-0.533', '0.516', '0.1448']",,,C535756,,,,
mondo:0012638,microphthalmia-brain atrophy syndrome,"['MOBA', 'microphthalmia syndromic 10', 'syndromic microphthalmia type 10', 'MCOPS10', 'MOBA syndrome', 'microphthalmia, syndromic 10', 'microphthalmia and brain atrophy']",0111812,611222,77299,,,,,C566985,,,,
mondo:0012639,hereditary spastic paraplegia 18,"['intellectual disability, motor dysfunction, and Joint contractures', 'spastic paraplegia 18, autosomal recessive', 'autosomal recessive spastic paraplegia type 18', 'SPG18', 'ERLIN2 autosomal recessive complex spastic paraplegia', 'hereditary spastic paraplegia type 18', 'intellectual disability, motor dysfunction and joint contractures', 'autosomal recessive spastic paraplegia 18', 'autosomal recessive complex spastic paraplegia caused by mutation in ERLIN2', 'spastic paraplegia 18']",0110771,611225,209951,,"['-0.4958', '0.1364', '-0.004646', '-0.5234', '0.358', '-0.854', '-0.4797', '0.6367', '-1.263', '-0.07666', '-0.585', '0.2715', '0.5107', '-0.605', '0.3557', '-0.278', '0.03207', '-0.3748', '-0.2079', '-0.4338', '0.3577', '-0.538', '0.354', '0.12494', '0.2773', '0.1755', '0.02797', '0.09106', '0.01974', '-0.46', '0.2035', '0.10095', '0.8325', '-0.1274', '-0.0944', '-0.015366', '0.2164', '-0.285', '0.02965', '-0.02739', '0.534', '-0.539', '-0.1415', '0.399', '-0.1318', '-0.2119', '-0.358', '0.3022', '0.463', '-0.03445', '0.2032', '0.063', '-0.4043', '-0.08844', '-0.5986', '-0.342', '0.08453', '-0.02826', '-0.1091', '0.7793', '-0.0986', '0.2029', '0.4963', '0.1365', '-0.1462', '0.273', '0.1569', '0.66', '-0.5347', '0.296', '-0.06244', '0.1305', '-0.0479', '-0.125', '0.2646', '-0.02533', '0.1426', '0.4048', '-0.2227', '-0.1096', '0.0488', '-0.1659', '0.359', '0.853', '-0.4285', '-0.014595', '0.1019', '0.6636', '0.4275', '0.2477', '0.1151', '0.5894', '0.4297', '0.1508', '0.406', '0.5493', '0.692', '-0.1602', '0.5947', '0.0651']",,,C567628,,,,
mondo:0012640,Charcot-Marie-Tooth disease type 4J,"['FIG4 Charcot-Marie-Tooth disease type 4', 'autosomal recessive Charcot-Marie-Tooth disease type 4J', 'Charcot-Marie-Tooth disease, type 4J', 'Charcot-Marie-Tooth disease, autosomal recessive, type 4J', 'CMT4J', 'Charcot-Marie-Tooth disease type 4 caused by mutation in FIG4']",0110184,611228,139515,C1970011,"['0.1666', '0.291', '0.2379', '0.1527', '-0.02116', '-0.125', '0.12427', '0.6646', '-0.9307', '0.04248', '0.07697', '0.3015', '-0.2957', '0.05054', '-0.01733', '-0.536', '-0.147', '-0.3152', '-0.3875', '-0.563', '0.0947', '0.2222', '0.5356', '0.4724', '0.2281', '0.47', '0.007233', '0.1791', '0.11017', '-0.2507', '-0.1086', '-0.6323', '0.09705', '0.1975', '0.2172', '-0.8477', '-0.5806', '-0.0734', '0.333', '-0.388', '-1.647', '-0.4775', '-0.3914', '0.7134', '-0.2242', '-0.3271', '-0.04556', '-0.0771', '-0.04367', '0.1376', '0.1874', '0.1572', '-0.1526', '-1.173', '0.259', '-0.3613', '-0.1659', '0.3247', '-0.5874', '0.10455', '-0.514', '0.5576', '0.899', '0.901', '-1.018', '0.901', '-0.138', '1.06', '-0.6514', '0.4565', '-1.0205', '0.1941', '0.459', '-0.3008', '1.14', '0.589', '-0.3206', '0.3489', '0.311', '-0.368', '-0.1174', '-0.1736', '0.8135', '0.6846', '0.1038', '-0.1063', '-0.02934', '0.67', '0.5503', '0.2607', '0.6055', '-0.1122', '0.02309', '0.6313', '0.4507', '0.652', '0.5024', '-0.516', '-0.02003', '0.4065']",C134954,,C566984,,,,
mondo:0012641,"restless legs syndrome, susceptibility to, 5","['restless legs syndrome 5', 'RLS5', 'RLS 5', 'restless legs syndrome, susceptibility to, 5']",,611242,,,,,,,,,,
mondo:0012642,major affective disorder 4,"['MAJOR affective disorder 4', 'major affective disorder 4', 'bipolar affective disorder', 'MAFD4']",,611247,,,,,,C567073,,,,
mondo:0012643,hereditary spastic paraplegia 32,"['hereditary spastic paraplegia type 32', 'autosomal recessive spastic paraplegia 32', 'autosomal recessive spastic paraplegia type 32', 'spastic paraplegia 32, autosomal recessive', 'SPG32', 'spastic paraplegia 32']",0110783,611252,171622,C4511958,,,,C566983,,,,
mondo:0012644,asphyxiating thoracic dystrophy 2,"['ATD2', 'asphyxiating thoracic dystrophy 2', 'SRTD2', 'short-rib thoracic dysplasia 2 with or without polydactyly', 'asphyxiating thoracic dystrophy type 2', 'Jeune syndrome caused by mutation in IFT80', 'IFT80 Jeune syndrome']",0110086,611263,,C1970005,,,,C566982,,,,
mondo:0012645,"glaucoma 1, open angle, N","['glaucoma 1, open angle, N', 'JOAG1N', 'GLC1N']",,611274,,C1969812,,,,C566977,,,,
mondo:0012648,isobutyryl-CoA dehydrogenase deficiency,"['Acad8 deficiency', 'acyl-CoaA dehydrogenase family, member 8, deficiency of', 'isobutyryl-CoA dehydrogenase deficiency', 'acyl-Coa dehydrogenase family, member 8, deficiency of', 'isobutyric aciduria', 'IBD deficiency']",,611283,79159,C1969809,"['-0.3604', '0.0837', '-0.253', '0.2732', '0.2318', '-0.383', '-0.3486', '0.578', '0.01263', '-0.02977', '0.1251', '-0.1913', '0.2257', '-0.359', '-0.3462', '-0.0168', '-0.1483', '-0.08795', '-0.481', '-0.434', '0.1519', '-0.3428', '0.229', '0.01828', '0.1598', '-0.1031', '0.1893', '0.11194', '-0.013565', '-0.05487', '0.3354', '0.0006633', '0.4028', '0.0706', '-0.4243', '-0.3584', '0.08014', '-0.4116', '0.05127', '-0.001685', '0.02022', '-0.3945', '0.4763', '-0.1453', '-0.2695', '-0.1392', '0.01909', '0.06854', '0.08386', '-0.1521', '-0.06152', '-0.3167', '-0.08057', '0.08', '-0.04022', '0.03818', '0.5195', '0.01877', '-0.551', '0.2014', '0.099', '0.1274', '0.554', '-0.2742', '-0.0917', '0.01011', '0.2612', '0.2822', '-0.4624', '0.01098', '-0.1602', '-0.01475', '-0.222', '0.2632', '0.1119', '0.308', '-0.1028', '-0.2186', '-0.058', '0.1362', '0.4707', '0.332', '0.04752', '0.0382', '0.437', '0.3833', '0.1959', '0.1025', '0.5366', '0.03223', '0.2854', '-0.01717', '-0.2605', '-0.3735', '0.5864', '0.57', '0.0753', '-0.5264', '-0.2014', '-0.2988']",C129975,,C535541,,,,
mondo:0012650,Cernunnos-XLF deficiency,"['SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with microcephaly, Growth retardation, and sensitivity to ionising radiation', 'SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, and sensitivity to ionizing radiation due to Nhej1 deficiency', 'Cernunnos XLFD', 'severe combined immunodeficiency with sensitivity to ionising radiation due to Nhej1 deficiency', 'combined immunodeficiency-microcephaly-growth retardation-sensitivity to ionizing radiation syndrome', 'Nhej1 syndrome', 'Cernunnos deficiency', 'SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, and sensitivity to ionising radiation due to Nhej1 deficiency', 'combined immunodeficiency-microcephaly-growth retardation-sensitivity to ionising radiation syndrome', 'NHEJ1 deficiency', 'severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionising radiation', 'severe combined immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation', 'SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with microcephaly, Growth retardation, and sensitivity to ionizing radiation', 'severe combined immunodeficiency with sensitivity to ionizing radiation due to Nhej1 deficiency']",,611291,169079,C1969799,"['-0.0672', '0.2832', '0.365', '-0.6934', '0.2026', '-0.0368', '0.3982', '0.09344', '0.006107', '-0.883', '-0.03055', '0.3303', '0.407', '-0.12085', '-0.3284', '0.1665', '0.06683', '-0.0169', '-0.4297', '-0.3796', '0.1462', '-0.2583', '0.704', '-0.2632', '0.2534', '0.3591', '-0.717', '-0.199', '-0.2498', '-0.4065', '0.2974', '0.483', '0.9844', '0.3777', '0.508', '0.2925', '-0.2191', '-0.4028', '-0.3726', '-0.314', '0.1306', '0.0976', '0.1696', '-0.1975', '-0.01767', '-0.846', '-0.0925', '-0.3535', '-0.4988', '-0.522', '-0.03424', '-0.8286', '0.3276', '0.612', '-0.06726', '0.12396', '0.1017', '-0.0653', '0.07654', '0.4463', '-0.2351', '0.05157', '-0.1991', '0.2059', '0.556', '0.1738', '0.549', '0.05414', '-0.44', '0.5723', '-0.2186', '-0.177', '0.0458', '0.5083', '0.579', '-0.03564', '0.1964', '-0.4211', '-0.2795', '0.12177', '0.07794', '0.0838', '-0.03485', '0.5845', '-0.3442', '-0.1797', '0.7686', '0.3552', '0.4236', '0.233', '0.5845', '0.05667', '-0.00868', '0.1368', '0.604', '1.182', '0.05365', '-0.62', '0.6514', '-0.0601']",,,C566970,,,,
mondo:0012651,spastic ataxia 2,"['SPG58', 'autosomal recessive spastic ataxia type 2', 'spastic ataxia type 2', 'SPAX2', 'KIF1C spastic ataxia', 'autosomal recessive spastic paraplegia type 58', 'spastic ataxia caused by mutation in KIF1C', 'spastic ataxia 2, autosomal recessive']",0050941,611302,397946,C1969796,"['-0.1327', '-0.1013', '-0.03653', '-0.0929', '-0.3284', '-1.107', '0.0185', '-0.2227', '-0.7427', '-0.863', '0.1299', '0.1879', '-0.0384', '0.235', '0.5005', '-0.2766', '-0.1884', '-0.3176', '0.1327', '-0.782', '0.05096', '-0.2769', '0.377', '-0.4424', '0.5923', '-0.261', '-0.3157', '0.2148', '0.11554', '-0.8696', '0.0886', '0.35', '-0.573', '0.04926', '0.4192', '0.02937', '-0.1018', '0.2275', '0.5356', '0.4673', '0.4067', '-0.00952', '-0.5015', '0.5796', '0.4402', '-0.563', '0.003', '0.437', '0.4053', '-0.02974', '-0.2021', '0.2166', '-0.2478', '-0.3767', '-0.1116', '-0.88', '0.282', '0.542', '-0.2189', '0.5605', '-0.58', '0.3657', '0.2798', '-0.1666', '-0.5303', '0.5737', '0.2301', '0.4993', '-0.624', '0.576', '0.8228', '0.555', '0.0225', '-0.7935', '0.89', '0.328', '0.2297', '0.215', '0.2035', '0.385', '-0.3838', '-0.8003', '0.7207', '0.715', '-0.3752', '-0.8384', '0.1102', '-0.1602', '0.5405', '0.3376', '0.4756', '0.4412', '0.171', '0.1366', '1.121', '1.092', '0.5405', '0.5703', '-0.514', '0.06052']",,,C566969,,,,
mondo:0012652,autosomal recessive limb-girdle muscular dystrophy type 2L,"['autosomal recessive limb-girdle muscular dystrophy caused by mutation in ANO5', 'limb-girdle muscular dystrophy type 2L', 'ANO5 autosomal recessive limb-girdle muscular dystrophy', 'LGMD2L', 'muscular dystrophy, limb-girdle, autosomal recessive 12', 'muscular dystrophy, limb-girdle, type 2L']",0110284,611307,206549,C1969785,"['0.2135', '-0.771', '-0.735', '-0.1628', '0.427', '-1.261', '-0.0808', '0.874', '-1.873', '-1.047', '0.2502', '0.4038', '-0.3918', '1.192', '0.4246', '0.00215', '-0.925', '-0.7363', '-0.3762', '-0.907', '-0.1335', '0.01863', '0.4297', '0.4685', '0.251', '-0.0812', '-0.1119', '-0.8154', '0.254', '-0.29', '0.9956', '-0.03976', '0.2642', '-0.05475', '0.2178', '0.08093', '-0.524', '0.5215', '0.1715', '-0.4104', '0.0868', '-0.678', '-0.599', '0.4387', '-0.1514', '0.363', '-0.10657', '0.4695', '0.05023', '0.6543', '0.1543', '-0.0649', '0.04208', '-0.7734', '0.3088', '-0.7676', '0.708', '0.681', '-0.0668', '0.01013', '0.02156', '-0.07996', '-0.1267', '-0.0912', '-0.10065', '-0.013466', '0.0984', '0.567', '-0.5186', '-0.41', '-0.1453', '0.2314', '0.2156', '-0.11414', '0.6895', '0.6304', '-0.1785', '0.1915', '0.2544', '0.1147', '0.0828', '-0.03098', '0.1947', '0.2893', '0.0879', '0.362', '-0.247', '-0.4426', '1.1', '-0.10236', '-0.5107', '0.0647', '0.5273', '0.8823', '0.2333', '-0.0738', '0.2722', '-0.2158', '-0.0785', '-0.1431']",,,C566968,,,,
mondo:0012653,"persistent hyperplastic primary vitreous, autosomal dominant","['PHPVAD', 'persistent hyperplastic primary vitreous, autosomal dominant']",,611308,,C1969784,,,,,,,,
mondo:0012654,atrial septal defect 4,"['atrial heart septal defect type 4', 'ASD4', 'atrial septal defect type 4', 'atrial septal defect 4', 'TBX20 atrial heart septal defect', 'atrial heart septal defect caused by mutation in TBX20']",0110109,611363,,C1969657,,,,C566963,,,,
mondo:0012655,"myoclonic epilepsy, juvenile, susceptibility to, 4","['myoclonic epilepsy, juvenile, 4', 'EJM4', 'myoclonic epilepsy, juvenile, susceptibility to, 4']",0111327,611364,,C1969656,,,,,,,,
mondo:0012656,lethal congenital contracture syndrome 3,"['PIP5K1C lethal congenital contracture syndrome', 'lethal congenital contractural syndrome 3', 'multiple contracture syndrome, Israeli Bedouin type B', 'lethal congenital contracture syndrome 3', 'LCCS3', 'lethal congenital contracture syndrome type 3', 'lethal congenital contracture syndrome caused by mutation in PIP5K1C', 'Israeli Bedouin type B multiple contracture syndrome']",0060653,611369,137783,C4275144,,,,C566961,,,,
mondo:0012657,Mungan syndrome,"['pseudoobstruction chronic idiopathic intestinal with Barrett esophagus and cardiac abnormalities', 'visceral neuromyopathy familial with pseudoobstruction megaduodenum Barrett esophagus and cardiac abnormalities', 'visceral neuromyopathy familial with pseudoobstruction megaduodenum Barrett oesophagus and cardiac abnormalities', 'pseudoobstruction, chronic idiopathic intestinal, with Barrett esophagus and Cardiac abnormalities', 'visceral Neuromyopathy, familial, with pseudoobstruction, Megaduodenum, Barrett esophagus, and Cardiac abnormalities', 'pseudoobstruction, chronic idiopathic intestinal, with Barrett oesophagus and Cardiac abnormalities', 'MUNGAN syndrome', 'MGS', 'pseudoobstruction chronic idiopathic intestinal with Barrett oesophagus and cardiac abnormalities']",,611376,,,"['-0.00979', '0.02667', '0.01009', '-0.002728', '0.002167', '-0.03029', '-0.01028', '0.0159', '-0.01637', '-0.02127', '-0.00565', '-0.007523', '-0.00909', '0.010025', '-0.00863', '-0.01706', '0.004723', '0.005486', '-0.01056', '-0.0352', '0.00787', '-0.00811', '0.0093', '-0.007805', '0.002436', '0.004097', '-0.005028', '-0.01104', '0.02026', '-0.00856', '0.02115', '-0.01006', '0.0351', '0.0232', '0.0075', '-0.01123', '0.002335', '-0.01018', '-0.002817', '-0.0287', '0.0219', '-0.02374', '0.007088', '-0.01967', '0.01317', '-0.02893', '-0.01278', '0.0219', '0.01034', '0.00869', '-0.01335', '-0.01046', '0.003769', '0.003342', '-0.002684', '-0.0004954', '0.01743', '0.00445', '-0.02353', '0.002876', '0.00295', '0.01436', '-0.005146', '0.00957', '0.008545', '-0.008896', '0.01775', '0.0104', '-0.02252', '0.02748', '-0.02388', '0.01001', '0.01288', '-0.01198', '0.003645', '0.0183', '0.006496', '-0.00877', '-0.02621', '-0.01337', '0.010025', '-0.003298', '-0.003242', '0.02495', '0.002327', '-0.00673', '0.002985', '0.0203', '0.03165', '0.01345', '0.008415', '0.02898', '-0.006863', '-0.00286', '0.0398', '0.01692', '0.0176', '-0.03732', '-0.001399', '0.01476']",,,C548078,,,,
mondo:0012658,brachydactyly type B2,"['BDB2', 'brachydactyly, type B2']",0110975,611377,140908,C1969652,"['-0.3755', '-0.2778', '0.5625', '-0.2927', '0.3787', '-0.4766', '-0.0377', '0.563', '-0.3623', '-0.4072', '-0.4324', '-0.3193', '-0.4438', '0.208', '-0.3467', '-0.18', '0.492', '-0.504', '-0.0915', '-0.2168', '0.2477', '-0.1675', '0.4006', '0.0788', '0.812', '0.454', '0.03482', '0.1436', '0.05948', '-0.1636', '0.2085', '-0.1703', '0.1436', '0.1464', '0.1599', '-0.7866', '-0.189', '-0.1686', '-0.4854', '-0.4966', '-0.1229', '-0.4355', '0.4377', '0.04764', '0.1649', '-0.441', '-0.2622', '0.2886', '0.02834', '0.2113', '0.02528', '-0.2778', '0.1632', '-0.0791', '-0.6426', '-0.684', '0.1242', '-0.1088', '-0.3923', '-0.2544', '0.099', '-0.1908', '-0.02347', '-0.178', '-0.11884', '-0.03038', '-0.0189', '0.4397', '-0.1512', '0.01651', '-0.84', '0.162', '0.2944', '-0.0723', '0.698', '0.4014', '0.2428', '-0.03735', '-0.1449', '-0.0201', '-0.1279', '-0.0943', '0.3416', '0.6143', '-0.2168', '0.2041', '-0.0802', '0.566', '-0.02432', '-0.1772', '-0.02602', '0.5186', '0.2722', '0.358', '0.3657', '-0.3425', '0.624', '-0.945', '0.4832', '0.3965']",,,,,,,
mondo:0012659,age related macular degeneration 9,"['age related macular degeneration type 9', 'C3 age-related macular degeneration', 'age-related macular degeneration caused by mutation in C3', 'macular Degeneration, age-related, type 9', 'macular degeneration, age-related, 9', 'ARMD9']",0110021,611378,,C1969651,,,,C566958,,,,
mondo:0012660,"susceptibility to visceral leishmaniasis, 2","['KAZA2', 'kala-AZAR, susceptibility to, 2', 'leishmaniasis, visceral, susceptibility to, 2']",,611381,,,,,,,,,,
mondo:0012661,"susceptibility to visceral leishmaniasis, 3","['leishmaniasis, visceral, susceptibility to, 3', 'KAZA3', 'kala-AZAR, susceptibility to, 3']",,611382,,,,,,,,,,
mondo:0012662,Usher syndrome type 2D,"['Usher syndrome type IID', 'Usher syndrome caused by mutation in WHRN', 'Usher syndrome, type 2D', 'USH2D', 'USHER syndrome, type IID', 'WHRN Usher syndrome']",0110840,611383,,,,,,,,H35.5,,
mondo:0012664,spastic ataxia 3,"['spastic ataxia type 3', 'autosomal recessive spastic ataxia with leukoencephalopathy', 'MARS2 autosomal recessive spastic ataxia', 'spastic ataxia 3, autosomal recessive', 'autosomal recessive spastic ataxia type 3', 'ARSAL', 'autosomal recessive spastic ataxia caused by mutation in MARS2', 'SPAX3']",0050942,611390,314603,CN230089,"['-0.1088', '-0.351', '0.04205', '0.06866', '-0.3257', '-1.059', '0.1605', '-0.006588', '-0.828', '-1.056', '0.09485', '0.1575', '-0.286', '0.3003', '0.633', '-0.369', '-0.0996', '-0.03876', '0.04596', '-0.8906', '-0.09625', '-0.3425', '0.173', '-0.7993', '0.5176', '-0.4915', '-0.516', '0.3335', '-0.1959', '-0.93', '0.1434', '0.475', '-0.688', '-0.1434', '0.6274', '0.1148', '-0.2114', '0.1792', '0.544', '0.4353', '0.2305', '0.2546', '-0.419', '0.4387', '0.6147', '-0.6597', '0.224', '0.3877', '0.441', '-0.1621', '0.02614', '0.2551', '-0.0658', '-0.3467', '-0.1957', '-0.937', '0.3499', '0.6743', '-0.0665', '0.569', '-0.5596', '0.2063', '0.3496', '-0.1846', '-0.6084', '0.487', '0.3044', '0.5356', '-0.4922', '0.4827', '0.811', '0.594', '-0.0508', '-0.908', '0.725', '0.3887', '0.2301', '0.3252', '0.0206', '0.614', '-0.3135', '-0.8687', '0.2097', '0.931', '-0.273', '-0.8857', '0.256', '0.0185', '0.653', '0.493', '0.4253', '0.4785', '0.2186', '0.1609', '1.156', '1.118', '0.3552', '0.4758', '-0.5356', '-0.2101']",,,C566956,,G11.4,,
mondo:0012665,cataract 33,"['cataract type 33', 'CTRCT33', 'cataract 33', 'cataract 33, multiple types', 'cortical cataract 33', 'BFSP1 early-onset non-syndromic cataract', 'early-onset non-syndromic cataract caused by mutation in BFSP1', 'cataract 33, cortical']",0110264,611391,217052,C3808107,"['-0.3423', '0.1562', '0.00606', '0.1693', '0.00417', '-0.2583', '-0.0663', '0.398', '-0.381', '-0.273', '-0.0337', '-0.154', '-0.1871', '0.164', '0.02287', '-0.2106', '0.0891', '-0.0791', '0.0631', '-0.502', '0.12476', '-0.010345', '0.00896', '-0.08374', '0.0716', '0.09796', '-0.02232', '0.0711', '-0.05768', '0.1442', '0.0961', '-0.1189', '0.2087', '0.2395', '0.0616', '0.0395', '0.11017', '-0.1699', '-0.0473', '-0.2659', '0.3066', '-0.252', '-0.00804', '0.2168', '-0.1388', '-0.362', '0.069', '-0.11487', '0.25', '-0.02715', '0.289', '0.03836', '0.08716', '0.0127', '-0.0373', '-0.333', '0.502', '0.04703', '-0.274', '0.04883', '0.1781', '-0.0501', '0.1798', '-0.02728', '-0.177', '0.2703', '0.3877', '0.3064', '0.04654', '0.08655', '-0.3782', '0.1125', '0.27', '0.0624', '0.0913', '0.03854', '0.0891', '0.1499', '-0.316', '0.0839', '-0.1548', '0.1266', '-0.01996', '0.1902', '0.1451', '-0.327', '0.2347', '0.2394', '0.1375', '0.2778', '0.259', '0.2445', '0.07117', '-0.12', '0.3462', '-0.11346', '0.4841', '-0.2695', '0.1583', '-0.009926']",,,C566955,,,,
mondo:0012666,"asthma-related traits, susceptibility to, 6","['asthma-related traits, susceptibility to, 6', 'ASRT6', 'asthma-related traits, susceptibility to, type 6']",,611403,,,,,,,,,,
mondo:0012667,dilated cardiomyopathy 1W,"['cardiomyopathy, dilated, type 1W', 'VCL familial isolated dilated cardiomyopathy', 'familial isolated dilated cardiomyopathy caused by mutation in VCL', 'dilated cardiomyopathy type 1W', 'CMD1W', 'cardiomyopathy, dilated, 1W']",0110446,611407,,C1969639,,,,C566954,,,,
mondo:0012668,Tented eyebrows,['Tented eyebrows'],,611426,,,,,,,,,,
mondo:0012669,Legius syndrome,"['neurofibromatosis type 1-like syndrome', 'neurofibromatosis 1-like syndrome', 'neurofibromatosis type 1 like syndrome', 'NF1-like syndrome', 'Legius syndrome']",,611431,137605,C1969623,"['0.2756', '0.0454', '0.2324', '-0.473', '0.639', '-0.1225', '0.06143', '0.48', '-0.5547', '-0.4666', '0.37', '-0.06226', '-0.1727', '0.1993', '0.569', '0.444', '0.3108', '-0.11755', '-0.0454', '-0.588', '-0.0257', '-0.2017', '0.3398', '-0.6567', '-0.584', '0.527', '0.014084', '-0.57', '0.3936', '-0.05487', '0.7217', '-0.525', '0.3298', '0.4146', '-0.1884', '0.03424', '-0.473', '-0.2646', '0.00848', '-0.2483', '0.696', '-0.3652', '0.1759', '0.06995', '0.781', '-0.254', '0.3083', '0.4092', '0.2054', '0.1957', '-0.1978', '0.2708', '-0.3496', '-0.0757', '-0.0871', '0.471', '0.0736', '-0.3718', '-0.5493', '0.1904', '0.2852', '0.1794', '-0.1614', '-0.4114', '0.4563', '0.4365', '0.1427', '0.2394', '-0.3975', '0.9185', '0.01445', '-0.335', '-0.3948', '-0.1459', '0.2023', '0.01063', '-0.5117', '-0.403', '-0.754', '-0.65', '0.6147', '0.2151', '0.05075', '0.3481', '-0.452', '-0.2091', '0.3357', '0.5825', '0.593', '0.3987', '0.4958', '0.4392', '-0.3555', '-0.2969', '0.444', '-0.585', '0.4426', '0.2086', '0.513', '0.1478']",C176941,,C548032,709.09,,,
mondo:0012670,autosomal recessive nonsyndromic hearing loss 63,"['autosomal recessive nonsyndromic deafness 63', 'deafness, autosomal recessive type 63', 'autosomal recessive nonsyndromic deafness caused by mutation in LRTOMT', 'autosomal recessive deafness 63', 'deafness, autosomal recessive 63', 'LRTOMT autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 63', 'DFNB63']",0110515,611451,,C1969621,,,,C566951,,,,
mondo:0012671,"tremor, hereditary essential, 3","['tremor, hereditary essential, 3', 'essential tremor, hereditary, 3', 'ETM3']",0111430,611456,,C1969617,,,,C566949,,,,
mondo:0012672,cholelithiasis,"['gallbladder disease 4', 'gallbladder disease type 4', 'gallstones', 'GBD4']",10211,611465,,C0947622,"['-0.1454', '0.09424', '0.10046', '-0.03717', '0.02971', '-0.1144', '-0.04816', '0.12213', '-0.07495', '0.01895', '-0.0594', '-0.0423', '0.04193', '0.04956', '-0.09595', '-0.08795', '-0.00708', '-0.01645', '-0.0885', '-0.2588', '0.03683', '-0.1267', '0.05893', '-0.0719', '0.07983', '-0.07404', '0.051', '0.00778', '0.06128', '-0.1357', '0.1239', '-0.06696', '0.1262', '0.0314', '0.04745', '-0.06143', '-0.0665', '-0.001762', '-0.001164', '-0.0903', '0.03177', '-0.12054', '0.1306', '-0.01767', '-0.09174', '-0.11456', '-0.0089', '0.0287', '0.02293', '0.1378', '-0.0835', '-0.01886', '0.03072', '0.02043', '-0.077', '-0.014305', '0.1045', '-0.0962', '-0.1947', '0.0454', '0.1724', '0.07355', '-0.0639', '-0.03455', '-0.000413', '-0.007156', '0.1566', '0.1337', '-0.04773', '0.1461', '-0.082', '0.005817', '0.0318', '-0.09564', '0.008484', '-0.02351', '0.05304', '-0.001699', '-0.1079', '-0.07263', '-0.0851', '-0.01184', '-0.005276', '0.08386', '-0.05905', '-0.006546', '0.03528', '0.0771', '0.1321', '-0.05185', '0.03574', '0.0704', '-0.0719', '0.02396', '0.2228', '-0.001914', '0.0946', '-0.2163', '-0.0585', '0.07245']",C122822,0004799,D002769,574.5,,,
mondo:0012673,"colorectal cancer, susceptibility to, 2","['colorectal cancer, susceptibility to, on chromosome 8Q24', 'colorectal cancer, susceptibility to, 2', 'CRCS2']",,611469,,,,,,,,,,
mondo:0012674,age related macular degeneration 10,"['macular Degeneration, age-related, type 10', 'TLR4 age-related macular degeneration', 'macular degeneration, age-related, 10', 'ARMD10', 'age related macular degeneration type 10', 'age-related macular degeneration caused by mutation in TLR4']",0110022,611488,,C1969108,,,,C566935,,,,
mondo:0012675,corticosteroid-binding globulin deficiency,"['Cbg deficiency', 'CBG deficiency', 'corticosteroid-binding globulin deficiency', 'Transcortin deficiency', 'corticosteroid-binding globulin, elevated', 'transcortin deficiency']",0090030,611489,199247,C1852529,"['-0.7983', '-0.08466', '-0.5254', '-0.01799', '0.1918', '-0.1287', '-0.6587', '0.0582', '-0.3315', '-0.01276', '-0.3052', '-0.07544', '0.4214', '0.5874', '0.2617', '0.1592', '0.2922', '0.5093', '-0.464', '-0.5376', '0.05276', '-0.323', '0.6533', '-0.1772', '-0.184', '0.09827', '-0.001376', '0.02902', '0.349', '0.01662', '0.728', '0.1132', '0.468', '-0.3018', '-0.05133', '-0.5054', '-0.1825', '0.2428', '0.65', '-0.2524', '-0.2524', '-0.01646', '0.02774', '-0.5884', '-0.1456', '-0.6274', '-0.3457', '-0.4824', '0.3047', '0.5923', '0.00931', '-0.08954', '0.256', '-0.00851', '-0.06165', '0.4053', '0.179', '-0.578', '-0.2474', '0.4285', '-0.006966', '0.2318', '0.2961', '-0.5806', '-0.5635', '0.0417', '0.1855', '0.5747', '-0.0814', '-0.02525', '-0.6123', '-0.1881', '-0.2089', '-0.0646', '0.49', '0.2194', '0.2632', '0.4817', '0.0779', '0.01505', '0.128', '-0.5366', '0.2075', '0.09576', '-0.2003', '0.2668', '0.331', '-0.1271', '0.6504', '0.3948', '0.1799', '-0.2103', '-0.4182', '-0.1896', '0.928', '0.258', '-0.3076', '-0.3706', '-0.4377', '0.3667']",,,,,,,
mondo:0012676,autosomal recessive osteopetrosis 4,"['osteopetrosis autosomal recessive 4', 'OPTB4', 'infantile malignant osteopetrosis 2', 'autosomal recessive malignant osteopetrosis caused by mutation in CLCN7', 'autosomal recessive osteopetrosis type 4', 'osteopetrosis, infantile malignant 2', 'CLCN7 autosomal recessive malignant osteopetrosis', 'osteopetrosis infantile malignant 2', 'CLCN7 autosomal recessive osteopetrosis', 'osteopetrosis, autosomal recessive 4', 'osteopetrosis, autosomal recessive type 4']",0110944,611490,,,,,,C566933,,,,
mondo:0012677,"atrial fibrillation, familial, 4","['KCNE2 familial atrial fibrillation', 'familial atrial fibrillation caused by mutation in KCNE2', 'atrial fibrillation, familial, 4', 'ATFB4', 'atrial fibrillation, familial, type 4']",,611493,,C1862394,,,,C566244,,,,
mondo:0012678,"atrial fibrillation, familial, 5","['atrial fibrillation, familial, 5', 'ATFB5']",,611494,,C1969099,,,,C566932,,,,
mondo:0012679,autosomal recessive osteopetrosis 6,"['OPTB6', 'autosomal recessive osteopetrosis intermediate form', 'osteopetrosis autosomal recessive 6', 'intermediate osteopetrosis', 'osteopetrosis autosomal recessive intermediate form', 'osteopetrosis, autosomal recessive, Intermediate form', 'PLEKHM1 osteopetrosis (disease)', 'autosomal recessive intermediate osteopetrosis', 'osteopetrosis, autosomal recessive type 6', 'autosomal recessive osteopetrosis type 6', 'osteopetrosis, autosomal recessive 6']",0110945,611497,210110,C1969093,"['-0.3071', '0.1412', '0.4636', '-0.3684', '0.02138', '-0.01755', '-0.2319', '0.565', '0.156', '-0.1414', '-0.2698', '0.01733', '-0.00281', '-0.0097', '0.226', '-0.2585', '0.2174', '-0.1329', '-0.00784', '-0.4326', '0.4153', '-0.1991', '0.5674', '-0.03564', '-4.166e-05', '0.0659', '0.06055', '0.0733', '-0.1539', '-0.0902', '-0.1505', '0.06866', '0.2678', '0.1794', '0.0504', '-0.11316', '0.01889', '-0.7993', '-0.142', '-0.4858', '0.09406', '-0.0636', '0.2798', '-0.4631', '-0.08966', '-0.5337', '0.06067', '0.003777', '0.1523', '-0.1753', '0.3215', '-0.1395', '0.1871', '0.2372', '0.05368', '-0.5845', '0.1046', '0.1981', '-0.251', '-0.09717', '0.004677', '-0.1754', '-0.4941', '-0.4692', '0.01953', '0.03326', '0.4133', '0.5747', '-0.177', '0.2996', '-0.2301', '-0.1823', '0.0681', '-0.4324', '-0.04773', '-0.0981', '-0.0876', '0.365', '0.2612', '-0.2585', '-0.336', '-0.2957', '-0.00841', '0.435', '-0.4016', '0.04785', '0.3223', '0.2605', '0.3264', '-8.95e-05', '0.004604', '0.03119', '-0.02527', '-0.00966', '0.5547', '0.3198', '0.431', '0.1249', '0.1375', '-0.04297']",,,C566931,,,,
mondo:0012680,nephronophthisis 7,"['nephronophthisis type 7', 'nephronophthisis 7', 'NPHP7', 'GLIS2 nephronophthisis (disease)']",0111116,611498,,C1969092,,,,C566930,,,,
mondo:0012681,"febrile seizures, familial, 7","['febrile seizures, familial, 7', 'FEB7', 'febrile convulsions, familial, 7']",0111311,611515,,C1969087,,,,C566929,,,,
mondo:0012682,immunodeficiency 35,"['immunodeficiency 35', 'hyper-IgE syndrome with atypical Mycobacteriosis, autosomal recessive', 'immunodeficiency type 35', 'HIES with atypical Mycobacteriosis, autosomal recessive', 'autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency caused by mutation in TYK2', 'TYK2 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a partial deficiency', 'IMD35', 'autosomal recessive hyper-IgE syndrome due to TYK2 deficiency', 'tyrosine kinase 2 deficiency', 'TYK2 deficiency']",0111989,611521,331226,C1969086,"['0.03772', '-0.02168', '-0.344', '-0.377', '0.104', '-0.4211', '0.407', '-0.6294', '-0.1361', '-0.0885', '-0.207', '0.0661', '-0.58', '0.02187', '0.1929', '0.08136', '-0.1923', '0.3474', '-0.278', '-0.6626', '0.00866', '-0.1328', '0.4463', '-0.03235', '-0.0764', '0.2764', '-0.2524', '0.1818', '0.1294', '-0.3652', '0.2944', '0.2942', '0.12305', '0.2151', '0.1041', '-0.2097', '-0.3994', '-0.08417', '0.00925', '-0.4053', '0.2384', '-0.2222', '0.484', '0.1584', '-0.1401', '-0.482', '0.2673', '0.02904', '0.1755', '-0.0626', '-0.0638', '-0.0689', '0.2214', '0.01198', '-0.4958', '-0.1212', '0.1339', '-0.1757', '-0.159', '0.03864', '0.501', '0.3584', '-0.06805', '0.02917', '0.6353', '0.1176', '0.1827', '0.05157', '-0.3374', '0.4236', '-0.2343', '-0.02417', '-0.313', '-0.435', '0.464', '-0.01035', '0.5522', '0.232', '0.2876', '-0.003119', '-0.7544', '-0.007168', '0.0811', '0.3', '-0.0086', '0.1504', '0.2908', '0.3335', '0.0799', '-0.02737', '0.1569', '0.285', '-0.11487', '-0.406', '0.872', '0.747', '0.7393', '-0.3384', '-0.1137', '-0.2224']",,,C566928,,,,
mondo:0012683,pontocerebellar hypoplasia type 6,"['PCH6', 'encephalopathy, fatal infantile, with mitochondrial respiratory chain defects', 'encephalopathy fatal infantile with mitochondrial respiratory chain defects', 'non-syndromic pontocerebellar hypoplasia caused by mutation in RARS2', 'pontocerebellar hypoplasia, type 6', 'RARS2 non-syndromic pontocerebellar hypoplasia', 'fatal infantile encephalopathy with mitochondrial respiratory chain defects']",0060275,611523,166073,C1969084,"['-0.389', '0.777', '-0.0163', '0.03096', '0.3162', '-0.9854', '0.05566', '0.8716', '-0.8745', '-0.472', '-0.7085', '-0.4854', '-0.6465', '-0.7085', '0.5005', '0.3394', '0.4768', '-0.6865', '0.09106', '-1.273', '-0.1439', '-0.3296', '0.3103', '-0.1483', '-0.1257', '0.0347', '-0.05447', '-0.07654', '-0.2216', '0.2406', '-0.05222', '0.5273', '0.4321', '0.1453', '-0.1226', '0.06494', '-0.1552', '0.3533', '-0.3086', '0.5127', '0.3188', '-0.5264', '0.02414', '0.322', '-0.4153', '0.04788', '-0.1475', '-0.1082', '0.2336', '-0.4146', '0.02289', '-0.5156', '-0.406', '-0.185', '0.01683', '-0.04654', '0.5684', '-0.1199', '0.1659', '0.6333', '-0.09937', '0.257', '1.048', '0.2336', '-0.3508', '-0.12256', '0.4712', '0.4312', '-1.169', '0.5386', '0.2', '0.525', '-0.00124', '0.07776', '0.2603', '0.319', '0.1104', '0.03122', '-0.6616', '0.491', '-0.04166', '0.2479', '0.354', '0.295', '0.3245', '0.2103', '-0.2167', '0.653', '0.4624', '-0.2993', '0.09436', '0.491', '-0.0785', '-0.4111', '0.5986', '0.4407', '0.667', '-0.349', '0.608', '-0.04602']",,,C548074,,,,
mondo:0012684,arrhythmogenic right ventricular dysplasia 12,"['arrhythmogenic right ventricular dysplasia, familial, type 12', 'ARVC12', 'JUP familial isolated arrhythmogenic right ventricular dysplasia', 'arrhythmogenic right ventricular dysplasia type 12', 'familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in JUP', 'familial arrhythmogenic right ventricular dysplasia 12', 'ARVD12', 'arrhythmogenic right ventricular cardiomyopathy 12', 'arrhythmogenic right ventricular dysplasia, familial, 12']",0110083,611528,,C1969081,,,,C566925,,,,
mondo:0012685,major affective disorder 5,"['MAFD5', 'major affective disorder 5', 'bipolar affective disorder', 'MAJOR affective disorder 5']",,611535,,,,,,C567074,,,,
mondo:0012686,major affective disorder 6,"['MAFD6', 'MAJOR affective disorder 6', 'bipolar affective disorder', 'major affective disorder 6']",,611536,,,,,,C567075,,,,
mondo:0012687,familial cavitary optic disk anomaly,"['CODA', 'familial CODA', 'cavitary optic DISC anomalies']",,611543,464760,C1969063,,,,C566924,,,,
mondo:0012688,cataract 17 multiple types,"['early-onset non-syndromic cataract caused by mutation in CRYBB1', 'CTRCT17', 'cataract, congenital nuclear, autosomal recessive 3', 'CATCN3', 'autosomal recessive congenital nuclear cataract 3', 'cataract 17, multiple types', 'CRYBB1 early-onset non-syndromic cataract', 'cataract 17, multiple types, with or without microcornea']",0110270,611544,98991,C1969062,,,,C566923,,,,
mondo:0012689,premature ovarian failure 5,"['primary ovarian failure caused by mutation in NOBOX', 'premature ovarian failure 5', 'NOBOX primary ovarian failure', 'premature ovarian failure type 5', 'Pof5']",0080862,611548,,C1969060,,,,C566921,,,,
mondo:0012690,Noonan syndrome 5,"['Noonan syndrome caused by mutation in RAF1', 'RAF1 Noonan syndrome', 'Noonan syndrome type 5', 'Noonan syndrome 5', 'NS5', 'RAF1 gene related Noonan syndrome']",0060583,611553,,C1969057,,C176933,,C548083,,,,
mondo:0012691,LEOPARD syndrome 2,"['leopard syndrome 2', 'Leopard syndrome type 2', 'LEOPARD syndrome 2', 'LPRD2']",0080549,611554,,C1969056,,,,C537117,,,,
mondo:0012692,"renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies","['renal tubular acidosis, distal, with nephrocalcinosis, short stature, mental retardation, and distinctive facies', 'renal tubular acidosis, distal, with nephrocalcinosis, short stature, intellectual disability, and distinctive facies']",,611555,,C1969055,,,,C566918,,,,
mondo:0012693,glycogen storage disease due to muscle and heart glycogen synthase deficiency,"['glycogen storage disease 0, muscle', 'muscle glycogen synthase deficiency', 'GSD due to muscle and heart glycogen synthase deficiency', 'glycogenosis type 0b', 'glycogen storage disease type 0, muscle', 'glycogen storage disease due to glycogen synthase deficiency of heart', 'glycogen storage disease type 0b', 'GSD 0B', 'GSD0B', 'GSD type 0b', 'heart glycogen storage disease due to glycogen synthase deficiency', 'glycogenosis due to muscle and heart glycogen synthase deficiency', 'muscle glycogen storage disease 0']",,611556,137625,C1969054,"['-0.3655', '0.03818', '-0.3215', '0.635', '0.295', '-0.84', '0.1923', '1.347', '-0.3262', '-0.2206', '-0.04672', '-0.3394', '-0.0762', '-0.2566', '0.3247', '0.0555', '-0.5146', '-0.03912', '-0.683', '-0.278', '0.6304', '-0.4758', '0.3723', '-0.1252', '0.2805', '-0.1142', '-0.004433', '0.7505', '-0.2285', '-0.1707', '0.9307', '0.01662', '0.4202', '-0.0533', '-0.334', '-0.5977', '0.2678', '-0.2092', '0.2391', '-0.493', '0.1023', '-0.04333', '0.5356', '0.239', '0.00734', '0.4072', '-0.00888', '0.4358', '-0.1344', '-0.02873', '-0.1537', '-0.3635', '0.10156', '0.3357', '0.4167', '-0.982', '0.2347', '0.1118', '-0.1862', '0.05066', '-0.0817', '0.3167', '0.3184', '-0.2966', '-0.6836', '-0.003218', '0.192', '0.568', '-0.984', '-0.3303', '-0.08844', '0.5713', '0.2188', '0.2023', '0.3418', '0.1508', '-0.4187', '0.4895', '-0.5356', '0.591', '-0.094', '0.1907', '-0.01585', '-0.1853', '0.316', '-0.01761', '0.7114', '0.4373', '0.6143', '0.1466', '0.318', '-0.007473', '0.03418', '-0.2698', '0.7944', '0.4543', '0.05716', '-0.0819', '-0.2397', '-0.3777']",,,C566917,,,,
mondo:0012694,Joubert syndrome 7,"['JBTS7', 'Joubert syndrome type 7', 'Joubert syndrome caused by mutation in RPGRIP1L', 'Joubert syndrome 7', 'RPGRIP1L Joubert syndrome']",0111002,611560,220497,C1969053,,C159653,,C566916,,,,
mondo:0012695,"Meckel syndrome, type 5","['Meckel syndrome, type 5', 'Meckel-Gruber syndrome, type 5', 'Meckel syndrome 5', 'MKS5', 'RPGRIP1L Meckel syndrome', 'Meckel syndrome caused by mutation in RPGRIP1L']",0070119,611561,,C1969052,,,,C566915,,,,
mondo:0012696,otosclerosis 4,"['otosclerosis 4', 'OTSC4']",,611571,,C1969046,,,,C566914,,,,
mondo:0012697,otosclerosis 7,"['otosclerosis 7', 'OTSC7']",,611572,,C1969044,,,,C566913,,,,
mondo:0012698,Waardenburg syndrome type 2E,"['SOX10 Waardenburg syndrome type 2', 'Waardenburg syndrome type 2E with or without neurologic involvement', 'Waardenburg syndrome type 2 caused by mutation in SOX10', 'hypogonadotropic hypogonadism with anosmia and deafness, with or without hypopigmentation', 'Waardenburg syndrome type IIE', 'WS2E with or without neurological involvement', 'hypogonadotropic hypogonadism with anosmia and deafness with or without hypopigmentation', 'Waardenburg syndrome, type 2E', 'WS2E', 'Waardenburg syndrome, type 2E, with or without neurologic involvement', 'Ws2E, with or without neurologic involvement']",0110956,611584,,C2700405,,,,,,,,
mondo:0012699,autosomal recessive limb-girdle muscular dystrophy type 2M,"['limb-girdle muscular dystrophy type 2M', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 4', 'muscular dystrophy, limb-girdle, type 2M', 'LGMD2M', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in FKTN', 'FKTN autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy-dystroglycanopathy (limb-girdle) type C 4', 'LGMD-FKTN related', 'MDDGC4']",0110296,611588,206554,C1969040,"['-0.02856', '-0.5825', '-0.69', '-0.3325', '0.535', '-1.247', '0.1195', '0.9272', '-1.531', '-0.9233', '0.03558', '0.4507', '-0.3008', '0.913', '-0.015236', '0.4478', '-0.7954', '-0.424', '-0.3713', '-0.4854', '0.07043', '0.1449', '0.292', '0.469', '0.1702', '-0.0233', '-0.1328', '-0.964', '0.1704', '-0.2227', '0.701', '-0.1381', '0.6387', '0.03647', '0.0987', '0.05927', '-0.7324', '0.303', '-0.0525', '-0.177', '0.1683', '-0.5254', '-0.5234', '0.185', '-0.1531', '0.252', '0.0009713', '0.746', '-0.06445', '0.529', '0.1929', '-0.256', '0.2312', '-0.7437', '0.2742', '-0.5576', '0.288', '0.973', '-0.201', '0.10046', '0.1624', '0.01048', '0.08136', '-0.00755', '0.08466', '-0.0808', '0.0274', '0.577', '-0.292', '-0.3455', '-0.3125', '0.548', '0.00268', '-0.05316', '0.6577', '0.831', '0.04398', '0.343', '-0.0429', '0.03204', '-0.2737', '0.255', '0.00628', '0.0402', '-0.06155', '0.2822', '-0.041', '-0.4402', '0.7925', '0.2527', '-0.2428', '0.2184', '0.4172', '1.066', '0.01306', '0.2961', '0.4546', '-0.6035', '-0.1315', '-0.207']",,,C566912,,,,
mondo:0012700,"renal tubular acidosis, distal, 4, with hemolytic anemia","['RTA, distal, autosomal recessive, with hemolytic Anemia', 'renal tubular acidosis, distal, with hemolytic anemia', 'dRTA with anemia', 'distal renal tubular acidosis with anemia', 'renal tubular acidosis, distal, with normal Red cell morphology', 'renal tubular acidosis, distal, with hemolytic anaemia', 'distal renal tubular acidosis with anaemia', 'distal renal tubular acidosis 4 with hemolytic anemia', 'dRTA with anaemia', 'distal renal tubular acidosis 4 with hemolytic anaemia', 'RTA, distal, autosomal recessive, with hemolytic Anaemia']",,611590,93610,C1969038,"['-0.4832', '0.2404', '-0.02663', '0.4246', '0.4001', '0.2379', '-0.4167', '0.6343', '-0.3196', '-0.431', '0.9463', '-0.2847', '0.2147', '0.512', '-1.086', '-0.1365', '-0.4565', '0.13', '-0.2128', '-0.6274', '-0.03812', '-0.541', '0.3347', '-0.04834', '0.8174', '-0.5254', '0.02785', '-0.3518', '0.6567', '0.075', '0.0701', '0.10547', '0.5474', '0.4', '0.451', '-0.261', '-0.9', '-0.604', '0.375', '-0.2091', '-0.8467', '0.1697', '0.0312', '-0.59', '-0.673', '-1.026', '0.001877', '0.3882', '0.5835', '-0.4368', '0.3982', '0.339', '0.8193', '-0.4324', '0.472', '-0.8047', '5.865e-05', '0.3296', '-1.109', '0.1276', '0.2218', '0.1713', '-0.0728', '-0.3809', '-0.1602', '0.1925', '0.3652', '0.774', '-0.6426', '0.962', '1.053', '-0.422', '-0.4307', '-0.55', '0.272', '0.996', '0.2935', '0.3638', '0.1586', '0.4927', '-0.001708', '-0.03354', '0.2444', '0.03262', '0.4675', '-0.369', '-0.5903', '0.1013', '0.7954', '-0.3855', '0.8066', '0.3167', '0.006153', '-0.036', '0.5254', '0.7446', '0.6147', '0.1323', '0.1477', '-0.5737']",,,,,,,
mondo:0012701,cataract 12 multiple types,"['cataract 12, multiple types', 'CTRCT12']",0110239,611597,98992,,"['-0.0743', '0.1321', '0.0295', '0.05234', '0.12024', '-0.1422', '-0.04648', '0.2397', '-0.1769', '-0.12463', '-0.02386', '-0.0646', '-0.0009737', '0.0674', '-0.0797', '-0.02147', '0.0256', '-0.11707', '-0.0324', '-0.3684', '-0.05856', '-0.003899', '0.1041', '0.007374', '0.0519', '-0.04068', '-0.06335', '0.02136', '-0.00869', '-0.01439', '0.1462', '-0.06683', '0.128', '0.212', '-0.02226', '-0.04016', '0.0474', '-0.05453', '-0.04034', '-0.06033', '0.07886', '-0.0643', '0.0754', '0.03287', '-0.02138', '-0.0887', '-0.01576', '0.1329', '0.04834', '0.04758', '0.002146', '-0.1505', '0.06757', '-0.07745', '-0.06555', '-0.03564', '0.2666', '-0.05695', '-0.1426', '-0.07666', '0.0866', '0.006905', '0.0598', '0.06665', '-0.01573', '0.05853', '0.2527', '0.2272', '-0.108', '0.1503', '-0.08765', '0.11084', '0.1094', '-0.1809', '0.11487', '-0.02756', '0.06537', '-0.05634', '-0.1373', '-0.04028', '-0.0696', '0.04123', '-0.04324', '0.1316', '-0.0312', '-0.04324', '0.0692', '0.11206', '0.155', '0.0617', '0.09064', '0.207', '0.0859', '0.0329', '0.2917', '-0.04343', '0.1536', '-0.1936', '0.03375', '0.02681']",,,C566909,,,,
mondo:0012702,"celiac disease, susceptibility to, 6","['autoimmune disease, susceptibility to, 5', 'gluten-sensitive enteropathy, susceptibility to, 6', 'celiac disease, susceptibility to, 6', 'CELIAC6']",,611598,,,,,,,,,,
mondo:0012703,lissencephaly due to TUBA1A mutation,"['LIS3', 'lissencephaly 3']",,611603,171680,CN200289,"['-0.3203', '0.455', '0.353', '-0.3657', '0.2347', '-0.363', '0.10187', '0.2656', '-0.425', '-0.1414', '-0.634', '-0.3403', '-0.0594', '-0.329', '0.4907', '-0.2815', '-0.2356', '-0.03683', '-0.15', '-0.5938', '0.0961', '-0.08746', '0.3438', '-0.2328', '0.0882', '0.0481', '-0.015335', '0.2646', '0.0841', '-0.1436', '0.2302', '0.12317', '0.59', '-0.04956', '-0.2257', '-0.1212', '0.005943', '-0.0761', '-0.1661', '-0.09906', '0.04156', '-0.2192', '-0.03354', '0.1367', '-0.3188', '-0.3225', '0.244', '0.05627', '0.1247', '0.1182', '0.4568', '-0.3376', '-0.2485', '-0.1148', '-0.1318', '-0.05746', '0.2634', '0.148', '-0.05032', '0.3882', '-0.0689', '0.04504', '0.3557', '0.2252', '-0.0954', '0.1084', '0.1726', '0.171', '-0.4158', '0.1236', '0.1016', '0.4238', '-0.002853', '0.0496', '-0.04474', '0.1785', '0.601', '0.01653', '-0.307', '-0.11426', '-0.3845', '0.3557', '-0.0674', '0.2195', '-0.2335', '-0.1263', '0.1375', '0.572', '0.2573', '-0.2352', '0.2135', '0.3398', '-0.1682', '-0.368', '0.631', '0.1059', '0.4424', '-0.2659', '0.535', '0.03687']",C148461,,C566908,,,,
mondo:0012704,dilated cardiomyopathy 1X,"['cardiomyopathy, dilated, with mild or No proximal muscle weakness', 'familial isolated dilated cardiomyopathy caused by mutation in FKTN', 'FKTN familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 1X', 'CMD1X', 'cardiomyopathy, dilated, 1X', 'cardiomyopathy, dilated, type 1X', 'dilated cardiomyopathy with mild or no proximal muscle weakness']",0110444,611615,,C1969024,,,,C566907,,,,
mondo:0012705,familial temporal lobe epilepsy 3,"['familial mesial temporal lobe epilepsy', 'ETL3', 'familial temporal lobe epilepsy type 3', 'epilepsy, familial mesial temporal lobe', 'epilepsy, familial temporal lobe, 3', 'FMTLE']",0060750,611630,,C1968848,,,,C566903,,,,
mondo:0012706,familial temporal lobe epilepsy 4,"['ETL4', 'occipitotemporal lobe epilepsy and migraine with aura', 'EPOLM', 'familial temporal lobe epilepsy type 4', 'epilepsy, familial temporal lobe, 4', 'epilepsy, occipitotemporal lobe, and migraine with aura']",0060753,611631,,C1968847,,,,C566902,,,,
mondo:0012707,familial febrile seizures 9,"['febrile seizures, familial, 9', 'febrile convulsions, familial, 9', 'FEB9']",0111303,611634,,C1968846,,,,C566901,,,,
mondo:0012708,"primary lateral sclerosis, adult, 1","['PLSA1', 'Pls, adult', 'primary lateral sclerosis, ADULT, 1']",,611637,,,,,,C566900,,,,
mondo:0012709,"microphthalmia, isolated, with coloboma 5","['microphthalmia, isolated, with coloboma 5', 'MCOPCB5', 'microphthalmia, isolated, with coloboma caused by mutation in Shh', 'microphthalmia with coloboma 5', 'Shh microphthalmia, isolated, with coloboma', 'microphthalmia, isolated, with coloboma type 5', 'SHH microphthalmia, isolated, with coloboma']",,611638,,C1968843,,,,C566899,,,,
mondo:0012710,"Hirschsprung disease, susceptibility to, 9","['HSCR9', 'Hirschsprung disease, susceptibility to, 9']",,611644,,,,,,,,,,
mondo:0012711,"peripapillary atrophy, beta type","['peripapillary atrophy, BETA type', 'peripapillary atrophy, beta type', 'PPAB', 'peripapillary chorioretinal atrophy, Beta type', 'Beta-PPA']",,611650,,C1968838,,,,C566898,,,,
mondo:0012712,dystonia with cerebellar atrophy,"['DYTCA', 'dystonia with cerebellar atrophy']",,611694,,C2673697,,,,C567131,,,,
mondo:0012713,"spondylometaphyseal dysplasia, East African type","['spondylometaphyseal dysplasia, East African type', 'spondylometaphyseal dysplasia East-African type']",0112302,611702,,C2673686,,,,C535796,,,,
mondo:0012714,early-onset myopathy with fatal cardiomyopathy,"['Salih myopathy', 'myopathy, early-onset, with fatal cardiomyopathy', 'EOMFC', 'SALMY']",0081341,611705,289377,C2673677,,,,C567129,,,,
mondo:0012715,"migraine with or without aura, susceptibility to, 12","['MGR12', 'migraine with or without aura, susceptibility to, 12', 'migraine, with or without aura, susceptibility to, 12']",,611706,,,,,,,,,,
mondo:0012716,"spondyloepiphyseal dysplasia, Cantu type","['fantasy Island syndrome', 'spondyloepiphyseal dysplasia-brachydactyly-speech disorder syndrome', 'Tatoo dysplasia', 'spondyloepiphyseal dysplasia-brachydactyly and distinctive speech', 'tattoo dysplasia', 'SED-BDS', 'Sed-BDS']",0112287,611717,163654,C2673649,,,,C567128,,,,
mondo:0012717,renal hypomagnesemia 4,"['EGF primary hypomagnesemia', 'HOMG4', 'hypomagnesemia 4, renal', 'EGF familial primary hypomagnesemia', 'primary hypomagnesemia caused by mutation in EGF', 'renal hypomagnesemia type 4', 'hypomagnesemia, renal, Normocalciuric']",0060882,611718,,C2673648,,,,C567127,,,,
mondo:0012718,hypotonia with lactic acidemia and hyperammonemia,"['combined oxidative phosphorylation deficiency caused by mutation in MRPS22', 'combined oxidative phosphorylation defect type 5', 'MRPS22 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 5', 'COXPD5', 'combined oxidative phosphorylation deficiency type 5']",0111473,611719,137908,C4510567,"['-0.7075', '0.573', '0.008575', '0.435', '-0.10297', '-0.8496', '-0.336', '0.871', '-0.2185', '-0.0691', '-0.714', '-0.594', '0.6953', '-0.03918', '0.00527', '0.04193', '-0.0145', '0.2008', '-0.5757', '-0.621', '-0.0764', '-0.06995', '0.742', '-0.02428', '0.0761', '0.1511', '-0.2524', '0.5425', '-0.05487', '-0.4546', '0.341', '0.1548', '0.563', '-0.2979', '-0.3577', '0.1459', '0.2328', '-0.1667', '0.0956', '0.1917', '-0.2488', '-0.523', '0.05975', '0.5093', '-0.4387', '0.1904', '-0.1809', '-0.05597', '0.1301', '0.1301', '-0.826', '-0.5527', '0.1754', '0.0539', '0.1879', '-0.879', '0.8823', '0.1553', '0.2491', '0.3555', '0.2167', '-0.01971', '0.525', '0.584', '-0.3245', '0.1498', '-0.0324', '0.635', '-0.7104', '0.0889', '0.6797', '0.5415', '0.011696', '0.0711', '-0.05524', '-0.00738', '0.451', '-0.007427', '-0.292', '0.656', '0.2362', '0.5596', '-0.10175', '0.03656', '0.02116', '0.2001', '0.3506', '1.052', '0.614', '0.1169', '0.3901', '0.1947', '0.1263', '0.141', '0.311', '0.2028', '-0.1512', '-1.054', '0.00324', '-0.328']",,,C567126,,,,
mondo:0012719,combined PSAP deficiency,"['prosaposin deficiency', 'combined prosaposin deficiency', 'combined SAP deficiency', 'combined saposin deficiency', 'combined Sap deficiency', 'encephalopathy due to prosaposin deficiency', 'PSAPD']",0111330,611721,139406,C4303785,"['-0.1477', '0.765', '-0.4368', '-0.125', '0.1846', '-0.8994', '0.5737', '0.1829', '0.01444', '-0.02733', '-0.0931', '0.1183', '-0.868', '-0.1294', '-0.00855', '0.4255', '-0.03656', '-0.04016', '-0.3726', '-0.852', '0.0489', '0.3115', '0.4375', '-0.0973', '-0.711', '-0.09784', '-0.3418', '0.2072', '-0.4019', '0.4175', '0.1561', '0.0664', '0.505', '0.22', '0.02791', '-0.0662', '-0.0894', '-0.0865', '-0.1527', '0.6323', '-0.3098', '-0.502', '0.6934', '-0.10803', '0.2454', '-0.01031', '-0.4731', '-0.08307', '-0.4146', '0.2961', '0.03546', '-0.0003033', '0.2363', '-0.0644', '0.376', '-0.7603', '-0.10126', '-0.03806', '0.5825', '0.1691', '-0.3652', '0.1519', '0.4956', '-0.4104', '-0.1132', '-0.1531', '0.7617', '0.4683', '-1.182', '0.1351', '-0.4382', '-0.0827', '-0.05838', '0.3684', '0.1398', '0.771', '0.4883', '0.34', '-0.12103', '0.1677', '-0.3445', '0.0212', '0.1063', '0.10834', '0.462', '0.2615', '0.553', '0.8306', '1.003', '0.615', '0.3933', '-0.0853', '0.13', '0.3', '0.6304', '1.183', '0.2396', '-0.4575', '0.586', '-0.33']",,,C567125,,,,
mondo:0012720,Krabbe disease due to saposin A deficiency,"['saposin A deficiency', 'Krabbe disease, atypical due to saposin A deficiency', 'Krabbe disease, atypical', 'Krabbe disease, atypical, due to saposin A deficiency']",,611722,,C2673266,,,,C567097,,,,
mondo:0012721,progressive myoclonic epilepsy type 3,"['PME type 3', 'EPM3', 'epilepsy, progressive myoclonic, 3, with or without intracellular inclusions', 'ceroid lipofuscinosis, neuronal, 14', 'KCTD7 progressive myoclonic epilepsy', 'progressive myoclonic epilepsy 3', 'EPM 3', 'progressive myoclonus epilepsy type 3', 'epilepsy progressive myoclonic type 3', 'epilepsy, progressive myoclonic 3, with or without intracellular inclusions', 'progressive myoclonic epilepsy caused by mutation in KCTD7', 'progressive myoclonic epilepsy due to KCTD7 deficiency']",0111446,611726,263516,C2673257,"['0.974', '0.11334', '-0.2783', '-0.1783', '-0.4165', '-0.5366', '0.704', '0.2666', '-0.738', '-0.4136', '0.0295', '-0.2191', '-0.3833', '0.4233', '-0.06046', '0.03665', '-0.2217', '-0.5347', '-0.4963', '-0.5366', '-0.2251', '0.5737', '-0.00683', '-0.4119', '-0.3374', '-0.089', '-0.10565', '-0.066', '-0.633', '0.4548', '0.3933', '-0.699', '0.3154', '0.1562', '0.8257', '0.479', '0.012344', '-0.0727', '0.03494', '-0.4666', '-0.0634', '-0.5283', '-0.08777', '-0.3022', '-0.4663', '-0.752', '-0.2634', '0.2114', '0.6396', '0.676', '-0.09937', '0.0678', '-0.02109', '-0.472', '0.12494', '-0.296', '-0.1732', '0.01173', '-0.2212', '0.286', '-0.734', '0.5483', '0.7246', '-0.31', '-0.3396', '1.45', '0.4058', '0.1356', '-0.9434', '0.719', '1.132', '0.9175', '-0.04434', '-0.4563', '-0.10406', '0.5835', '1.022', '0.4465', '-0.4773', '0.3027', '-0.1349', '0.771', '0.4033', '0.308', '0.3381', '0.1305', '0.2247', '0.6924', '0.7646', '0.207', '0.001083', '-0.04626', '-0.4082', '0.05072', '0.0278', '0.144', '0.2507', '-0.6504', '0.2405', '0.3665']",,,C567095,,,,
mondo:0012722,Dauwerse-Peters syndrome,"['short stature, facial dysmorphism, severe brachydactyly and syndactyly', 'Dauwerse-Peters syndrome', 'short stature, Facial Dysmorphism, Severe brachydactyly, and syndactyly']",,611733,,C2673203,,,,C567093,,,,
mondo:0012723,Leber congenital amaurosis 10,"['LCA10', 'Leber congenital amaurosis type 10', 'Leber congenital amaurosis caused by mutation in CEP290', 'amaurosis congenita of Leber, type 10', 'CEP290 Leber congenital amaurosis', 'Leber congenital amaurosis 10']",0110291,611755,,,,,,C565720,,H35.5,,
mondo:0012724,familial cold autoinflammatory syndrome 2,"['FCAS2', 'NLRP12 familial cold autoinflammatory syndrome', 'NAPS12', 'NALP12-associated hereditary periodic fever syndrome', 'familial cold autoinflammatory syndrome type 2', 'NLRP12-associated hereditary periodic fever syndrome', 'familial cold autoinflammatory syndrome caused by mutation in NLRP12', 'familial cold autoinflammatory syndrome 2']",0090063,611762,247868,C3897034,"['0.00774', '-0.04404', '-0.4714', '-0.1628', '-0.07965', '-0.4866', '0.1844', '0.2612', '-0.2576', '0.1943', '0.02873', '0.66', '0.1746', '0.1296', '-0.2395', '0.353', '0.2407', '0.02452', '-0.1427', '-0.6245', '0.0804', '-0.3225', '0.01227', '-0.09064', '0.00218', '0.273', '-0.02087', '-0.1539', '-0.05966', '-0.1968', '-0.1028', '-0.191', '0.3508', '0.1526', '-0.1528', '0.3467', '-0.3882', '-0.174', '-0.04745', '0.07837', '-0.013', '-0.4846', '0.2056', '0.0746', '0.5366', '-0.11835', '-0.509', '0.229', '0.2947', '0.3591', '-0.659', '0.1197', '0.3792', '0.356', '0.1459', '0.1302', '0.3704', '-0.2258', '-0.3313', '-0.12006', '-0.0939', '0.5996', '0.07367', '-0.0406', '0.4763', '0.2133', '0.4045', '0.3958', '-0.2466', '0.6865', '-0.2605', '0.06137', '-0.2307', '-0.2092', '0.1622', '0.6025', '0.3757', '0.8184', '0.2893', '0.557', '0.2722', '-0.3042', '0.04736', '-0.2905', '0.2196', '-0.2201', '0.5854', '0.992', '0.01631', '0.3477', '0.328', '0.0532', '0.1554', '0.05182', '0.4983', '0.3352', '0.526', '-0.408', '-0.421', '-0.01032']",C119043,,C567090,,,,
mondo:0012725,lipoprotein glomerulopathy,"['lipoprotein glomerulopathy', 'LPG']",,611771,329481,C2673196,"['-0.05466', '-0.01258', '0.0558', '-0.04944', '0.03638', '-0.274', '-0.2576', '0.2394', '-0.04346', '0.12274', '-0.3523', '-0.1769', '0.006496', '-0.1057', '-0.1914', '-0.2815', '0.131', '0.08545', '0.07764', '-0.619', '0.0809', '-0.251', '0.289', '0.2123', '0.1738', '0.05838', '0.2073', '0.2935', '-0.0946', '-0.229', '0.621', '0.03186', '0.637', '0.010574', '-0.004555', '-0.451', '-0.0289', '0.0736', '0.0801', '-0.529', '-0.1311', '-0.03418', '0.518', '0.00435', '-0.0858', '-0.2297', '0.1113', '0.0524', '-0.1504', '-0.0672', '0.10046', '0.1132', '0.2998', '-0.1245', '-0.1725', '-0.01485', '0.2401', '-0.1473', '-0.455', '0.05978', '0.254', '0.1483', '0.1013', '-0.2277', '0.1719', '-0.1512', '0.3704', '0.2084', '-0.2874', '-0.02022', '-0.3489', '-0.1215', '0.03714', '0.3333', '0.1825', '-0.2327', '0.3848', '0.1587', '0.0337', '-0.09015', '-0.05118', '0.0445', '-0.12115', '0.1624', '-0.1318', '-0.10925', '0.2886', '-0.01036', '0.2465', '-0.0832', '0.4075', '-0.01246', '-0.4976', '0.08185', '0.3982', '0.4226', '0.3123', '-0.1388', '-0.1774', '0.2201']",,,C567089,593.89,,,
mondo:0012726,autosomal dominant familial hematuria-retinal arteriolar tortuosity-contractures syndrome,"['angiopathy, hereditary, with nephropathy, aneurysms, and muscle cramps', 'hereditary angiopathy with nephropathy, aneurysms, and muscle cramps syndrome', 'HANAC', 'hereditary angiopathy-nephropathy-aneurysms-muscle cramps syndrome', 'HANAC syndrome']",,611773,73229,C2673195,"['-0.377', '-0.2135', '-0.2383', '-0.06946', '0.1365', '-0.168', '0.12354', '0.4446', '-0.5347', '0.0829', '-0.477', '-0.4385', '0.1813', '-0.2072', '0.004612', '0.592', '0.01892', '-0.1284', '0.01458', '-0.6313', '-0.0656', '0.1755', '-0.04312', '-0.06586', '0.02702', '-0.0699', '0.04443', '0.232', '0.01636', '0.345', '0.2231', '0.013565', '0.7764', '-0.01906', '-0.1063', '-0.07745', '-0.2278', '-0.05923', '0.3792', '-0.4224', '0.2578', '-0.5825', '0.6963', '-0.6333', '0.678', '0.1185', '0.2595', '0.2776', '-0.3398', '-0.4575', '0.12177', '0.5293', '0.474', '-0.6597', '-0.1733', '-0.1445', '0.4512', '0.124', '-0.929', '-0.10156', '0.456', '-0.26', '-0.2394', '-0.881', '-0.6523', '-0.4136', '0.4998', '0.641', '-0.7324', '0.2445', '-0.2354', '-0.12115', '-0.1548', '0.086', '0.8345', '-0.0858', '0.0458', '-0.2551', '-0.1456', '0.1065', '0.3687', '0.622', '0.2742', '0.6963', '-0.2411', '0.0778', '0.5825', '0.3162', '-0.4355', '-0.4673', '0.0332', '0.1722', '-0.1009', '0.0983', '0.676', '0.04245', '0.774', '0.156', '-0.6567', '0.3918']",,,C567088,758.89,,,
mondo:0012727,mucocutaneous lymph node syndrome,"['Kawasaki disease', 'mucocutaneous lymph node syndrome', 'Kd', 'infantile polyarteritis', 'infantile polyarteritis nodosa', 'MLNS', 'Kawasaki syndrome', 'acute febrile mucocutaneous lymph node syndrome', 'Kawasaki^s disease', 'acute febrile MCLS', 'acute febrile mucocutaneous lymph node syndrome [MCLS]']",13378,611775,2331,C0026691,,C34825,0004246,D009080,446.1,,10023320,
mondo:0012728,Brugada syndrome 2,"['Brugada syndrome type 2', 'BRGDA2', 'GPD1L Brugada syndrome', 'Brugada syndrome 2', 'Brugada syndrome caused by mutation in GPD1L']",0110219,611777,,C2673193,,,,C567087,,,,
mondo:0012729,"erythrocytosis, familial, 4","['erythrocytosis, familial, type 4', 'ECYT4', 'familial polycythemia caused by mutation in EPAS1', 'EPAS1 familial polycythemia', 'erythrocytosis, familial, 4']",0080339,611783,,C2673187,,,,C567086,,,,
mondo:0012730,"aortic aneurysm, familial thoracic 6","['ACTA2 familial thoracic aortic aneurysm and aortic dissection', 'familial thoracic aortic aneurysm and aortic dissection caused by mutation in ACTA2', 'familial thoracic aortic aneurysm with livedo reticularis and iris flocculi', 'AAT6', 'aortic aneurysm, familial thoracic type 6', 'aortic aneurysm, familial thoracic 6']",,611788,,C2673186,,,,C567085,,,,
mondo:0012731,elliptocytosis 1,"['EPB41 hereditary elliptocytosis', 'EL1', 'elliptocytosis 1', '4.1- trait', 'hereditary elliptocytosis caused by mutation in EPB41', 'elliptocytosis, Rhesus-linked type', 'elliptocytosis-1', '4.1-minus trait', 'elliptocytosis type 1', 'Protein 4.1 of erythrocyte Membrane, defect of']",,611804,,C2678497,,,,C567520,,,,
mondo:0012732,"tremor, hereditary essential, and idiopathic normal pressure hydrocephalus","['ETINPH', 'tremor, hereditary essential, and idiopathic normal pressure hydrocephalus']",,611808,,C2678494,,,,C567519,,,,
mondo:0012733,autosomal recessive bestrophinopathy,"['bestrophinopathy, autosomal recessive', 'ARB', 'bestrophinopathy', 'retinopathy, Burgess-Black type']",0050662,611809,139455,C3888198,"['-0.451', '-0.4355', '-0.10596', '0.04715', '0.05606', '-0.2208', '0.09827', '0.9946', '-0.3857', '-0.7095', '-0.38', '-0.04593', '0.01968', '0.1768', '-0.7', '-0.10864', '0.5566', '-0.3733', '0.332', '-0.8667', '-0.4219', '-0.137', '-0.338', '0.04028', '-0.3274', '0.2654', '-0.4604', '0.4128', '-0.1798', '0.2034', '0.9395', '0.1078', '0.03918', '-0.0457', '-0.4727', '0.3142', '0.2283', '-0.7163', '-0.1505', '-0.1108', '0.2864', '-0.234', '0.3413', '-0.3984', '-0.2449', '0.2769', '-0.0963', '-0.338', '-0.2017', '0.2625', '0.7397', '-0.234', '0.09515', '-0.564', '0.0942', '-0.06647', '0.5327', '0.1918', '-0.3804', '-0.1888', '-0.2142', '0.1907', '0.2396', '0.09717', '-0.2793', '-0.4165', '0.576', '0.501', '-0.00935', '0.41', '-0.169', '-0.11884', '0.12256', '-0.2366', '1.181', '0.04388', '0.0773', '-0.4917', '0.2524', '-0.09155', '0.6025', '0.133', '0.2168', '1.265', '-0.3796', '0.3315', '0.0636', '0.08514', '0.2151', '0.1844', '0.04977', '0.673', '0.1489', '0.02014', '1.008', '-0.3167', '0.10095', '-0.705', '-0.11505', '-0.2222']",,,C567518,,H35.5,,
mondo:0012734,SERKAL syndrome,"['SERKAL syndrome', '46,XX SEX reversal with dysgenesis of kidneys, ADRENALS, and lungs', 'Sex reversion-kidneys, adrenal and lung dysgenesis syndrome', '46,XX Sex reversal with dysgenesis of kidneys Adrenals and lungs', 'SERKAL']",,611812,139466,C2678492,"['-0.4524', '0.2441', '0.10736', '-0.2676', '0.3792', '-0.3145', '-0.3005', '0.02449', '-0.3345', '-0.7026', '0.00646', '-0.2004', '-0.2942', '-0.06335', '0.0949', '-0.328', '0.155', '0.5513', '-0.2152', '-0.492', '-0.1265', '-0.136', '0.389', '-0.548', '0.1875', '-0.2401', '-0.2659', '0.2397', '0.5522', '-0.5254', '0.3801', '0.0981', '0.4788', '-0.3206', '-0.08417', '-0.3506', '-0.0994', '-0.2263', '-0.1068', '-7.09e-05', '0.0502', '-0.2235', '0.11487', '-0.321', '-0.0407', '-0.4045', '-0.0977', '0.0001222', '0.1058', '0.1561', '0.01794', '0.03687', '0.12494', '0.2368', '-0.4724', '-0.2197', '0.3767', '0.1068', '-0.2131', '0.03293', '0.3965', '0.2147', '0.258', '0.06027', '0.1703', '-0.399', '0.1561', '0.4905', '-0.769', '-0.2175', '-0.4065', '0.081', '0.12006', '0.2384', '-0.2268', '-0.1521', '-0.09', '0.1648', '-0.1626', '-0.09515', '-0.00941', '0.5327', '-0.0928', '0.0847', '-0.074', '0.02902', '0.386', '-0.023', '0.02962', '-0.01666', '-0.012566', '0.4155', '-0.12036', '-0.368', '0.8267', '-0.0976', '0.2925', '-0.3447', '-0.02066', '0.2356']",C123726,,C567517,,,,
mondo:0012735,Temple-Baraitser syndrome,"['TMBTS', 'mental retardation, severe, and absent nails of hallux and pollex', 'Temple-Baraitser syndrome', 'severe mental retardation and absent nails of hallux and pollex', 'severe intellectual disability and absent nails of hallux and pollex', 'intellectual disability, severe, and absent nails of hallux and pollex', 'severe intellectual disability-aplasia/hypoplasia of thumb and hallux syndrome']",,611816,420561,C2678486,"['0.1597', '-0.571', '0.01755', '-0.5894', '-0.006252', '-0.1699', '0.104', '1.18', '-0.9976', '-0.931', '-0.6553', '-0.2397', '0.461', '-0.2585', '-0.1484', '-0.2238', '0.55', '-0.674', '-0.5854', '-0.8403', '-0.11053', '-0.2184', '0.672', '0.7163', '0.2263', '-0.3013', '-0.1735', '-0.1371', '-0.1558', '-0.735', '1.104', '0.06067', '0.03625', '0.3015', '0.3013', '0.2761', '-0.858', '-0.1246', '-0.368', '-0.28', '0.315', '-0.492', '-0.3538', '-0.2377', '-0.01591', '-0.2769', '-0.10205', '0.66', '-0.2754', '0.0391', '-0.8994', '0.1681', '-0.6587', '0.1987', '-0.248', '-0.0714', '-0.3628', '-0.0749', '-0.003332', '0.2847', '-0.0718', '-0.05252', '-0.04736', '0.224', '-0.03464', '0.427', '0.03635', '0.1687', '-0.4224', '0.302', '-0.0786', '0.1099', '-0.1409', '0.1613', '-0.3794', '0.3135', '0.4065', '-0.9155', '-0.02097', '0.2404', '0.6626', '0.145', '-0.08636', '1.105', '0.2578', '0.04874', '-0.864', '0.7764', '-0.07574', '0.441', '0.0831', '-0.0003948', '0.2754', '0.194', '0.627', '-0.1879', '0.1262', '-0.7964', '0.2607', '0.296']",,0009062,C567516,,,,
mondo:0012736,long QT syndrome 9,"['CAV3 long QT syndrome', 'long QT syndrome 2/9, digenic', 'long QT syndrome 9, acquired, susceptibility to', 'long QT syndrome caused by mutation in CAV3', 'long QT syndrome type 9', 'long QT syndrome 9', 'LQT9']",0110650,611818,101016,,,,,C567515,,,,
mondo:0012737,long QT syndrome 10,"['long QT syndrome 10', 'LQT10', 'atrial fibrillation, familial, 17', 'long QT syndrome caused by mutation in SCN4B', 'long QT syndrome type 10', 'SCN4B long QT syndrome']",0110651,611819,334,C2678484,"['-0.00867', '0.0804', '0.0212', '-0.004383', '0.02165', '-0.08124', '0.0579', '0.168', '-0.0811', '-0.0892', '0.015205', '0.02237', '0.0408', '0.0341', '-0.077', '-0.07983', '0.03967', '-0.03784', '-0.00425', '-0.1473', '0.04904', '-0.0614', '0.0572', '-0.07355', '0.0505', '-0.07776', '-0.007732', '-0.01616', '0.02084', '-0.0596', '0.09106', '-0.01118', '0.10266', '0.0486', '0.01724', '-0.0777', '-0.00848', '-0.06137', '-0.02318', '-0.0843', '0.08417', '-0.1125', '0.0762', '-0.06573', '0.007378', '-0.07587', '-0.10565', '0.1328', '0.00961', '0.04553', '-0.01505', '-0.03113', '-0.02303', '0.04282', '-0.0761', '-0.0642', '0.05774', '-0.01366', '-0.0757', '0.0006094', '0.1096', '0.03625', '-0.00856', '0.00495', '0.001717', '-0.01197', '0.0851', '0.05804', '-0.10236', '0.1373', '-0.0951', '0.04752', '0.07996', '-0.1252', '0.002619', '0.07263', '0.011185', '-0.00517', '-0.06555', '-0.05145', '0.03105', '0.03522', '-0.02039', '0.06506', '-0.0204', '0.0377', '0.009766', '0.09467', '0.1041', '0.04187', '0.01744', '0.05026', '-0.013145', '0.055', '0.1868', '0.05148', '0.0905', '-0.2008', '-0.0451', '0.02591']",,,C567514,,,,
mondo:0012738,long QT syndrome 11,"['AKAP9 long QT syndrome', 'long QT syndrome 11', 'long QT syndrome caused by mutation in AKAP9', 'LQT11', 'long QT syndrome type 11']",0110652,611820,101016,C2678483,"['-0.01566', '0.0943', '0.0169', '-0.0285', '0.0018015', '-0.11383', '0.0446', '0.16', '-0.0686', '-0.05142', '-0.02054', '-0.000694', '0.07715', '-0.01139', '-0.0464', '-0.0699', '0.02345', '-0.0422', '0.0001545', '-0.1471', '0.03403', '-0.012566', '0.06573', '-0.05685', '0.0421', '-0.0765', '-0.02078', '-0.00586', '0.04507', '-0.07837', '0.1377', '-0.02661', '0.11896', '0.01366', '0.026', '-0.0931', '-0.002954', '-0.07715', '-0.01648', '-0.1256', '0.0719', '-0.1616', '0.05444', '-0.10516', '0.0254', '-0.08453', '-0.083', '0.1436', '-0.013756', '0.02434', '-0.02127', '-0.03482', '-0.01602', '0.0422', '-0.06635', '-0.05826', '0.05075', '-0.02072', '-0.06088', '0.0637', '0.09155', '0.0432', '-0.005016', '-0.01016', '0.00737', '0.02495', '0.06384', '0.0691', '-0.1042', '0.1461', '-0.1085', '0.012764', '0.05936', '-0.1003', '-0.03235', '0.066', '-0.00211', '-0.01973', '-0.06155', '-0.0385', '0.04773', '0.0496', '-0.03345', '0.05875', '0.0254', '0.0335', '-0.01686', '0.10754', '0.1287', '-0.01482', '0.003624', '0.03668', '-0.000605', '0.03494', '0.193', '0.04858', '0.1365', '-0.2251', '-0.046', '0.002617']",,,C567513,,,,
mondo:0012739,microtia-eye coloboma-imperforation of the nasolacrimal duct syndrome,"['microtia eye coloboma and imperforation of the nasolacrimal duct', 'microtia with nasolacrimal duct imperforation and eye coloboma', 'Balikova-Vermeesch syndrome']",,611863,139450,C2678482,,,,C567512,,,,
mondo:0012740,"chromosome 22q11.2 deletion syndrome, distal","['distal 22q11.2 microdeletion syndrome', 'chromosome 22q11.2 deletion syndrome, distal', 'distal del(22)(q11.2)', 'distal chromosome 22Q11.2 deletion syndrome', 'distal monosomy 22q11.2']",0060413,611867,261330,C4518343,,,,C567511,,,,
mondo:0012741,"prostate cancer, hereditary, 12","['EHBP1 familial prostate cancer', 'prostate cancer, hereditary, type 12', 'HPC12', 'prostate cancer, hereditary, 12', 'familial prostate cancer caused by mutation in EHBP1']",,611868,,C2678479,,,,C567510,,,,
mondo:0012742,Brugada syndrome 3,"['CACNA1C Brugada syndrome', 'Brugada syndrome caused by mutation in CACNA1C', 'Brugada syndrome type 3', 'BRGDA3', 'Brugada syndrome 3']",0110220,611875,,C2678478,,,,C567509,,,,
mondo:0012743,Brugada syndrome 4,"['Brugada syndrome 4', 'Brugada syndrome caused by mutation in CACNB2', 'Brugada syndrome type 4', 'CACNB2 Brugada syndrome', 'BRGDA4']",0110221,611876,,C2678477,,,,C567508,,,,
mondo:0012744,dilated cardiomyopathy 1Y,"['familial isolated dilated cardiomyopathy caused by mutation in TPM1', 'cardiomyopathy, dilated, type 1Y', 'CMD1Y', 'cardiomyopathy, dilated, 1Y', 'left ventricular noncompaction 9', 'TPM1 familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 1Y']",0110457,611878,,,,,,C567507,,,,
mondo:0012745,dilated cardiomyopathy 1Z,"['CMD1Z', 'cardiomyopathy, dilated, type 1Z', 'cardiomyopathy, dilated, 1Z', 'TNNC1 familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 1Z', 'familial isolated dilated cardiomyopathy caused by mutation in TNNC1']",0110434,611879,,C2678475,,,,C567506,,,,
mondo:0012746,dilated cardiomyopathy 2A,"['dilated cardiomyopathy type 2A', 'cardiomyopathy, dilated, autosomal recessive', 'CMD2A', 'cardiomyopathy, dilated, 2A', 'cardiomyopathy, congestive, autosomal recessive', 'cardiomyopathy, dilated, type 2A']",0110460,611880,,C2678474,,,,,,,,
mondo:0012747,glycogen storage disease due to aldolase A deficiency,"['Aldoa deficiency', 'Red cell aldolase deficiency', 'GSD 12', 'glycogen storage disease 12', 'glycogenosis type 12', 'glycogenosis type XII', 'aldolase deficiency red cell', 'glycogen storage disease type 12', 'aldolase deficiency, Red cell', 'GSD12', 'GSD due to aldolase A deficiency', 'GSD type XII', 'aldolase a deficiency', 'GSD type 12', 'glycogen storage disease XII', 'glycogenosis due to aldolase A deficiency', 'glycogen storage disease type XII']",,611881,57,C0272066,"['-0.564', '-0.01599', '-0.5415', '-0.0339', '0.3027', '-0.566', '-0.4373', '0.1909', '0.3145', '-0.298', '0.1268', '-0.1937', '-0.001446', '-0.03265', '-0.4282', '-0.3394', '-0.4111', '-0.386', '-0.6304', '-0.2625', '0.556', '-0.1065', '0.3176', '-0.07245', '-0.2942', '-0.2568', '0.02159', '-0.2386', '0.1819', '-0.1842', '-0.00805', '-0.0415', '0.039', '0.3513', '-0.4087', '-0.4863', '-0.434', '-0.2423', '-0.1394', '-0.2583', '0.1946', '-0.2908', '0.03885', '0.2316', '-0.3079', '0.1271', '0.03687', '0.03345', '-0.02313', '0.2102', '-0.0662', '0.03833', '0.8813', '0.3752', '0.3262', '-0.6787', '0.1085', '-0.1737', '-0.57', '0.2386', '0.4949', '-0.1935', '0.579', '-0.34', '-0.3699', '0.469', '0.273', '0.10077', '-0.5356', '0.0955', '0.07477', '-0.1323', '-0.283', '-0.1002', '0.03452', '0.5605', '0.448', '0.01562', '-0.4133', '0.3662', '-0.2742', '0.2065', '0.2264', '0.2151', '0.7837', '0.2102', '0.1334', '0.538', '0.4321', '0.2217', '0.4163', '0.2057', '0.2361', '-0.2094', '0.7944', '0.7983', '0.1848', '-0.1499', '-0.044', '0.0811']",,,C562718,282.3,,,
mondo:0012748,primary ciliary dyskinesia 7,"['ciliary dyskinesia, primary, type 7', 'primary ciliary dyskinesia caused by mutation in DNAH11', 'DNAH11 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 7, with or without situs inversus', 'CILD7', 'primary ciliary dyskinesia 7 with or without situs inversus', 'primary ciliary dyskinesia type 7', 'ciliary dyskinesia, primary, 7']",0110605,611884,,C2678473,,,,C567504,,,,
mondo:0012749,"mesomelic dysplasia, camera type","['mesomelic dysplasia, camera type']",,611886,,C2678472,,,,C567503,,,,
mondo:0012750,lethal arthrogryposis-anterior horn cell disease syndrome,"['LAAHD', 'congenital arthrogryposis with anterior horn cell disease', 'lethal arthrogryposis with anterior horn cell disease', 'Vuopala disease']",,611890,53696,C2678471,"['-0.4216', '0.1632', '0.4832', '-0.402', '-0.321', '-0.4043', '0.1794', '0.6733', '-0.563', '-0.3691', '-0.2118', '-0.2141', '-0.2097', '0.1083', '0.2217', '-0.028', '0.02151', '-0.1382', '0.03864', '-0.529', '0.1389', '-0.453', '0.0669', '-0.0937', '0.05203', '0.154', '-0.2258', '0.1143', '-0.1738', '-0.05618', '0.10547', '0.1908', '0.4329', '0.2263', '0.10547', '-0.0906', '-0.05658', '-0.02599', '0.00998', '-0.1718', '-0.4663', '-0.3242', '-0.3884', '0.2822', '-0.219', '-0.1831', '0.05353', '0.1803', '-0.0559', '0.06323', '-0.3784', '0.00853', '-0.1132', '0.04987', '-0.1372', '-0.4426', '-0.12054', '-0.1703', '0.1626', '0.1427', '0.04385', '0.05765', '-0.454', '0.1065', '-0.3933', '-0.0812', '0.4326', '0.194', '-0.2323', '0.4023', '-0.1951', '0.2017', '0.049', '-0.004425', '-0.09827', '0.005264', '0.0862', '0.0795', '-0.2578', '0.0743', '0.04318', '0.1592', '0.08514', '0.52', '-0.1505', '-0.162', '0.01634', '0.2198', '0.3896', '-0.00729', '0.1902', '0.4478', '0.3738', '0.2903', '0.475', '0.223', '0.08453', '0.02458', '0.4856', '0.253']",,,C567502,,,,
mondo:0012751,"aortic aneurysm, familial abdominal, 3","['aneurysm, familial abdominal 3', 'AAA3', 'aortic aneurysm, familial abdominal, 3']",,611891,,C2678470,,,,C567501,,,,
mondo:0012752,"aneurysm, intracranial berry, 6","['aneurysm, intracranial BERRY, 6', 'ANIB6']",0080969,611892,,C2678469,,,,C567500,,,,
mondo:0012753,amyotrophic lateral sclerosis type 9,"['ANG amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis caused by mutation in ANG', 'ALS9', 'amyotrophic lateral sclerosis 9', 'amyotrophic lateral sclerosis type 9']",0060200,611895,,C2678468,,,,C567499,,,,
mondo:0012754,nanophthalmos 3,"['Nanophthalmia 3', 'NNO3', 'nanophthalmos 3']",,611897,,C2678467,,,,C567498,,,,
mondo:0012755,episodic ataxia type 7,"['episodic ataxia, type 7', 'EA7']",0050995,611907,209970,C2677843,,,,C567459,,,,
mondo:0012756,proximal 16p11.2 microdeletion syndrome,"['autism susceptibility 14A', 'chromosome 16p11.2 deletion syndrome, 593kb', 'monosomy 16p11.2', 'proximal del(16)(p11.2)', 'chromosome 16p11.2 deletion syndrome, 593-KB', 'chromosome 16p11.2 deletion syndrome', 'microdeletion 16p11.2', 'autism, susceptibility to, 14A', 'Del(16)(p11.2)', '16p11.2 deletion syndrome', 'proximal monosomy 16p11.2']",,611913,261197,CN202166,,C120408,,C579850,758.39,,,
mondo:0012757,"lung fibrosis-immunodeficiency-46,XX gonadal dysgenesis syndrome","['immunodeficiency, ovarian dysgenesis, and pulmonary fibrosis']",,611926,137631,C3150156,,,,,,,,
mondo:0012758,"prostate cancer, hereditary, 13","['MSMB familial prostate cancer', 'prostate cancer, hereditary, type 13', 'prostate cancer, hereditary, 13', 'familial prostate cancer caused by mutation in MSMB', 'HPC13']",,611928,,C2677821,,,,C567456,,,,
mondo:0012759,"camptodactyly syndrome, Guadalajara type 3","['camptodactyly syndrome Guadalajara type 3', 'camptodactyly syndrome, Guadalajara, type 3', 'camptodactyly syndrome, Guadalajara, type III']",,611929,488434,C2677809,,,,C567455,,,,
mondo:0012760,"epilepsy, idiopathic generalized, susceptibility to, 5","['epilepsy, idiopathic generalized, susceptibility to, 5', 'EIG5', 'epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 10']",0111320,611934,,,,,,,,,,
mondo:0012761,chromosome 3q29 microduplication syndrome,"['trisomy 3q29', '3q29 microduplication', 'chromosome 3q29 DUPLICATION syndrome', 'microduplication 3Q29 syndrome', '3q29 microduplication syndrome']",0060459,611936,251038,C2749873,,,,C567626,,,,
mondo:0012762,catecholaminergic polymorphic ventricular tachycardia 2,"['ventricular tachycardia, stress-induced polymorphic', 'CASQ2 catecholaminergic polymorphic ventricular tachycardia', 'CVPT2', 'catecholaminergic polymorphic ventricular tachycardia type 2', 'ventricular tachycardia, catecholaminergic polymorphic, type 2', 'CPVT2', 'ventricular tachycardia, catecholaminergic polymorphic, 2', 'catecholaminergic polymorphic ventricular tachycardia caused by mutation in CASQ2']",0060676,611938,,C2677794,,C148368,,,,I47.2,,
mondo:0012763,"epilepsy, childhood absence, susceptibility to, 6","['epilepsy, childhood absence, susceptibility to, type 6', 'epilepsy, childhood absence, susceptibility to, 6', 'epilepsy, idiopathic generalized, susceptibility to, 6', 'CACNA1H childhood absence epilepsy', 'childhood absence epilepsy caused by mutation in CACNA1H', 'susceptibility to childhood absence epilepsy 6', 'ECA6']",,611942,,,,,,,,,,
mondo:0012764,RIDDLE syndrome,"['RNF168 deficiency', 'RIDDLE syndrome', 'radiosensitivity, immunodeficiency, dysmorphic features, and learning difficulties', 'radiosensitivity-immunodeficiency-dysmorphic features-learning difficulties syndrome']",0090113,611943,420741,C2677792,"['-0.4238', '0.01391', '0.308', '-0.6313', '0.488', '-0.3464', '-0.4204', '0.5005', '-0.574', '0.0536', '0.1721', '0.0387', '0.2039', '-0.2197', '0.5117', '0.2394', '0.1982', '-0.11676', '-0.4614', '-0.532', '0.3025', '-0.1393', '0.2522', '-0.07556', '0.2432', '0.1627', '-0.184', '-0.352', '0.1251', '-0.298', '0.286', '0.404', '0.48', '-0.000554', '-0.0331', '-0.2834', '-0.3577', '-0.243', '-0.1809', '-0.558', '0.1504', '-0.1293', '0.167', '-0.1917', '-0.34', '-0.5005', '0.0599', '-0.02367', '0.1791', '0.198', '-0.461', '0.137', '-0.2168', '0.295', '-0.2107', '-0.1765', '-0.11163', '-0.1777', '-0.2405', '0.266', '0.259', '0.1844', '0.169', '0.04514', '0.4097', '0.2974', '0.03894', '0.1553', '-0.5674', '0.3347', '-0.527', '-0.1853', '-0.148', '-0.07275', '0.179', '-0.02919', '0.3357', '0.001771', '0.08746', '0.1329', '0.2435', '0.0472', '0.04', '0.3457', '-0.377', '0.2006', '0.1736', '0.418', '0.613', '0.4465', '-0.1731', '0.2035', '-0.0382', '-0.162', '0.6157', '0.4644', '0.3135', '-0.0923', '0.325', '0.1737']",,0009055,C567453,,,,
mondo:0012765,lymphatic malformation 2,"['LMPH1B', 'lymphedema, hereditary, 1B']",0070211,611944,,C2677787,,,,C567452,,,,
mondo:0012766,hereditary spastic paraplegia 37,"['autosomal dominant spastic paraplegia type 37', 'hereditary spastic paraplegia type 37', 'autosomal dominant spastic paraplegia 37', 'SPG37', 'spastic paraplegia 37, autosomal dominant']",0110788,611945,171612,C2936880,,,,C567931,,,,
mondo:0012767,age related macular degeneration 11,"['age related macular degeneration type 11', 'macular degeneration, age-related, 11', 'macular Degeneration, age-related, type 11', 'ARMD11', 'age-related macular degeneration caused by mutation in CST3', 'CST3 age-related macular degeneration']",0110023,611953,,C2677774,,,,C567450,,,,
mondo:0012768,"prostate cancer, hereditary, 11","['prostate cancer, hereditary, 11', 'HPC11']",,611955,,C2677773,,,,C567449,,,,
mondo:0012769,"prostate cancer, hereditary, 14","['prostate cancer, hereditary, 14', 'HPC14']",,611958,,C2677772,,,,C567448,,,,
mondo:0012770,"prostate cancer, hereditary, 15","['prostate cancer, hereditary, 15', 'HPC15']",,611959,,C2677771,,,,C567447,,,,
mondo:0012771,"asthma-related traits, susceptibility to, 7","['inherited susceptibility to asthma caused by mutation in CHI3L1', 'asthma-RELATED traits, susceptibility to, 7', 'asthma-related traits, susceptibility to, 7', 'ASRT7', 'CHI3L1 inherited susceptibility to asthma', 'asthma-related traits, susceptibility to, type 7']",,611960,,,,,,,,,,
mondo:0012772,Stevenson-Carey syndrome,['Stevenson-Carey syndrome'],,611961,,C2677763,,,,C567446,,,,
mondo:0012773,Hunter-Macdonald syndrome,['Hunter-Macdonald syndrome'],,611962,,C2677745,,,,C567445,,,,
mondo:0012774,chromosome 15q13.3 microdeletion syndrome,"['monosomy 15q13.3', '15q13.3 microdeletion syndrome', 'Del(15)(q13.3)', 'microdeletion 15q13.3 syndrome', '15q13.3 microdeletion', 'chromosome 15q13.3 deletion syndrome', 'chromosome 15q13.3 microdeletion syndrome']",0060394,612001,199318,,,,,C567439,,,,
mondo:0012775,thrombocytopenia 4,"['THC4', 'thrombocytopenia 4', 'thrombocytopenia type 4', 'thrombocytopenia caused by mutation in CYCS', 'thrombocytopenia, autosomal dominant, 4', 'CYCS thrombocytopenia']",,612004,,C2677608,,,,C567438,,,,
mondo:0012776,"celiac disease, susceptibility to, 7","['CELIAC7', 'celiac disease, susceptibility to, 7', 'gluten-sensitive enteropathy, susceptibility to, 7']",,612005,,,,,,,,,,
mondo:0012777,"celiac disease, susceptibility to, 8","['celiac disease, susceptibility to, 8', 'CELIAC8', 'gluten-sensitive enteropathy, susceptibility to, 8']",,612006,,,,,,,,,,
mondo:0012778,"celiac disease, susceptibility to, 9","['celiac disease, susceptibility to, 9', 'CELIAC9', 'gluten-sensitive enteropathy, susceptibility to, 9']",,612007,,,,,,,,,,
mondo:0012779,"celiac disease, susceptibility to, 10","['CELIAC10', 'celiac disease, susceptibility to, 10', 'gluten-sensitive enteropathy, susceptibility to, 10']",,612008,,,,,,,,,,
mondo:0012780,"celiac disease, susceptibility to, 11","['CELIAC11', 'celiac disease, susceptibility to, 11', 'gluten-sensitive enteropathy, susceptibility to, 11']",,612009,,,,,,,,,,
mondo:0012781,"celiac disease, susceptibility to, 12","['celiac disease, susceptibility to, 12', 'gluten-sensitive enteropathy, susceptibility to, 12', 'CELIAC12']",,612010,,,,,,,,,,
mondo:0012782,"celiac disease, susceptibility to, 13","['celiac disease, susceptibility to, 13', 'CELIAC13', 'gluten-sensitive enteropathy, susceptibility to, 13']",,612011,,,,,,,,,,
mondo:0012783,RFT1-congenital disorder of glycosylation,"['carbohydrate deficient glycoprotein syndrome type In', 'CDG in', 'CDG syndrome type In', 'RFT1-CDG (CDG-In)', 'congenital disorder of glycosylation type In', 'CDG-In', 'CDG1N', 'Man5GlcNAc2-PP-Dol flippase deficiency', 'congenital disorder of glycosylation, type In', 'CDGIN', 'RFT1-CDG', 'congenital disorder of glycosylation type 1n']",0080566,612015,244310,C2677590,"['-0.2107', '0.1659', '0.4817', '-0.2457', '-0.4695', '-0.7114', '0.08026', '0.1433', '-0.4246', '-0.4119', '-0.2952', '-0.2264', '-0.07135', '-0.1377', '-0.616', '0.1566', '0.506', '-0.4834', '0.0398', '-0.4062', '0.3018', '-0.3655', '-0.2058', '0.01642', '0.4539', '0.2725', '-0.04437', '0.32', '-0.1388', '-0.1456', '0.257', '0.6284', '0.4285', '0.3652', '-0.2303', '-0.1437', '0.09454', '-0.2339', '-0.277', '-0.3896', '-0.3018', '0.1848', '-0.09717', '0.1102', '-0.000768', '-0.2452', '0.2632', '0.418', '0.144', '0.917', '-0.324', '0.04794', '-0.11414', '-0.0838', '-0.2494', '-0.11255', '0.1278', '0.1725', '-0.292', '0.4756', '-0.2644', '0.07025', '0.3975', '0.1346', '-0.2703', '-0.1522', '0.479', '0.01645', '-0.787', '0.1313', '-0.5415', '0.06445', '0.0736', '-0.1506', '0.2778', '-0.01662', '0.8857', '-0.00318', '0.2427', '0.000509', '0.2179', '-0.4114', '-0.0954', '0.1904', '0.1445', '-0.1713', '-0.158', '0.5054', '0.5728', '0.5244', '-0.1556', '0.552', '0.1522', '0.363', '0.0908', '0.742', '0.2156', '-0.2659', '0.567', '0.7153']",,,C567437,,,,
mondo:0012784,autosomal recessive ataxia due to ubiquinone deficiency,"['spinocerebellar ataxia, autosomal recessive 9', 'coenzyme Q10 deficiency, primary, type 4', 'autosomal recessive spinocerebellar ataxia 9', 'coenzyme Q10 deficiency, primary, 4', 'COQ10D4', 'autosomal recessive spinocerebellar ataxia type 9', 'autosomal recessive ataxia due to coenzyme Q10 deficiency', 'autosomal recessive cerebellar ataxia type 2', 'SCAR9', 'ARCA2']",0070241,612016,139485,C4511089,"['-0.10156', '-0.1635', '-0.03476', '0.1511', '-0.2634', '-0.921', '0.1415', '0.2356', '-0.4158', '-0.968', '0.1609', '0.3608', '-0.1338', '0.1549', '0.462', '-0.2074', '0.05292', '-0.0741', '0.06726', '-1.025', '-0.01118', '-0.4583', '0.2045', '-0.7095', '0.4255', '-0.5005', '-0.3323', '0.1857', '-0.0742', '-0.761', '0.10754', '0.364', '-0.6235', '-0.2732', '0.179', '-0.0395', '-0.1389', '0.1412', '0.4922', '0.588', '0.2081', '0.01793', '-0.396', '0.5474', '0.699', '-0.583', '0.441', '0.4263', '0.3545', '0.01193', '-0.2783', '0.0619', '0.027', '-0.3635', '-0.0936', '-0.6714', '0.1699', '0.4438', '0.02242', '0.537', '-0.7534', '0.2668', '0.2097', '-0.1907', '-0.2352', '0.623', '0.3198', '0.709', '-0.6304', '0.3962', '0.6753', '0.587', '-0.05853', '-0.7407', '0.5767', '0.3667', '0.4429', '0.4001', '0.0793', '0.6797', '-0.3145', '-0.7944', '0.3025', '0.8164', '-0.1346', '-0.543', '0.3157', '-0.05396', '0.4414', '0.7466', '0.592', '0.5586', '-0.006855', '-0.04364', '1.098', '0.8833', '0.2278', '0.3333', '-0.279', '-0.0768']",,,C567436,,,,
mondo:0012785,"pyloric stenosis, infantile hypertrophic, 3","['pyloric stenosis, infantile hypertrophic, 3', 'IHPS3']",,612017,,C2677588,,,,C567435,,,,
mondo:0012786,juvenile cataract-microcornea-renal glucosuria syndrome,"['cataract, juvenile, with microcornea and glucosuria', 'cataract 47, juvenile, with microcornea', 'CTRCT47', 'CJMG', 'cataract, juvenile, with microcornea and glucosuria, formerly', 'cataract 47', 'cataract, juvenile, with microcornea']",0070353,612018,247794,C2677587,"['-0.1711', '0.03613', '0.02483', '0.1228', '0.02913', '-0.1602', '-0.07306', '0.3628', '-0.2496', '-0.1755', '-0.193', '-0.359', '-0.2427', '-0.1765', '-0.1815', '-0.04684', '0.11584', '-0.022', '-0.02928', '-0.7773', '-0.207', '0.176', '-0.08136', '-0.2378', '0.3484', '0.2158', '-0.1123', '0.2698', '0.3787', '-0.1265', '0.4885', '-0.1779', '0.385', '0.2327', '0.4224', '-0.2742', '-0.4963', '-0.5728', '-0.2822', '-0.315', '-0.02324', '-0.3247', '0.4846', '-0.2532', '0.2081', '-0.2905', '-0.1262', '0.06824', '-0.459', '-0.2014', '0.1847', '0.1648', '0.01547', '-0.4248', '-0.0919', '-0.8975', '0.5645', '-0.00773', '-0.919', '0.0854', '0.579', '-0.4348', '0.3997', '-0.1797', '-0.0609', '-0.1958', '0.608', '0.3828', '-0.3518', '0.2932', '-0.3816', '-0.1962', '0.2166', '-0.02832', '0.1805', '-0.2812', '0.1393', '-0.0314', '-0.2487', '0.1471', '0.1821', '0.4937', '0.10986', '0.65', '0.1466', '-0.06476', '0.1373', '0.2336', '-0.01775', '0.05475', '0.1927', '0.3132', '0.1018', '-0.1292', '0.9014', '-0.2089', '0.784', '-0.4558', '-0.11957', '0.3384']",,,C567434,,,,
mondo:0012787,hereditary spastic paraplegia 39,"['NTE related motor neuron disorder', 'PNPLA6 hereditary spastic paraplegia', 'autosomal recessive spastic paraplegia type 39', 'hereditary spastic paraplegia caused by mutation in PNPLA6', 'spastic paraplegia due to neuropathy target esterase mutation', 'SPG39', 'spastic paraplegia 39', 'autosomal recessive spastic paraplegia 39', 'spastic paraplegia due to NTE mutation', 'spastic paraplegia 39, autosomal recessive', 'NTEMND', 'hereditary spastic paraplegia type 39', 'NTE-related motor neuron disorder']",0110790,612020,139480,C4304963,"['-0.2847', '0.4333', '0.00843', '0.05756', '0.2144', '-0.603', '-0.4465', '0.46', '-0.4033', '-0.3108', '-0.1708', '-0.1686', '0.0404', '-0.2625', '0.422', '0.03198', '0.00244', '-0.00609', '-0.1852', '-0.295', '0.2268', '-0.0879', '0.01822', '0.2783', '0.1787', '0.1411', '-0.0395', '-0.0291', '0.04333', '-0.4434', '0.306', '-0.0957', '0.2318', '-0.05927', '0.04132', '-0.5674', '0.1224', '-0.0961', '0.0968', '-0.08685', '-0.1567', '-0.8325', '-0.1382', '0.07214', '-0.169', '-0.3032', '-0.0751', '-0.05527', '-0.09534', '-0.597', '-0.2416', '-0.09143', '-0.09283', '0.04028', '0.069', '-0.525', '0.592', '0.0767', '-0.2233', '0.3105', '0.05142', '-0.1414', '0.4036', '0.1519', '-0.4612', '0.0278', '0.03004', '0.539', '-0.3923', '0.03058', '-0.381', '-0.1313', '-0.263', '-0.10614', '0.3809', '0.2317', '-0.3733', '0.5884', '-0.07574', '-0.0327', '0.3896', '0.495', '0.2603', '0.6045', '-0.1743', '0.04694', '0.1287', '0.2046', '0.1862', '-0.07477', '0.1874', '0.2135', '0.2646', '-0.1862', '0.803', '0.10144', '0.1544', '-0.6787', '-0.2563', '0.0696']",,,C567433,,,,
mondo:0012788,"coronary heart disease, susceptibility to, 9","['CHDS9', 'coronary heart disease, susceptibility to, 9']",,612030,,,,,,,,,,
mondo:0012789,dystonia 16,"['PRKRA dystonic disorder', 'dystonic disorder caused by mutation in PRKRA', 'dystonia type 16', 'dystonia 16', 'Young-onset dystonia-(parkinsonism)', 'DYT-PRKRA', 'DYT16', 'early-onset dystonia parkinsonism']",0090048,612067,210571,C2677567,"['0.4434', '0.334', '-0.01011', '-0.28', '-0.2676', '-1.13', '0.3005', '0.1827', '-0.62', '-0.2109', '0.7837', '0.6436', '-0.2196', '0.296', '0.311', '0.375', '-0.417', '-0.8794', '-0.4392', '-0.9727', '-0.4883', '-0.0983', '0.343', '-0.2465', '-0.4148', '0.02032', '-0.39', '0.282', '-0.141', '-0.3599', '0.2734', '0.446', '0.7417', '0.2676', '0.5527', '-0.0599', '0.5635', '-0.1833', '0.172', '-0.28', '0.4087', '-0.2181', '-0.561', '0.3828', '0.3972', '0.0307', '-0.1725', '0.11053', '0.323', '0.386', '0.2048', '0.05264', '0.6084', '0.2554', '0.6597', '-0.5806', '-0.07623', '0.693', '0.2764', '-0.0997', '-0.869', '-0.3767', '0.2258', '-0.2194', '-1.017', '0.512', '0.07916', '-0.05243', '-0.4915', '0.5728', '-0.5425', '-0.1829', '0.0154', '0.2051', '0.3625', '0.511', '0.6426', '0.1554', '0.0909', '-0.4502', '0.10126', '0.4094', '0.4146', '0.4526', '0.9395', '0.2632', '0.1924', '0.5747', '1.819', '0.2395', '0.4644', '0.3882', '0.3638', '-0.08044', '1.03', '-0.1214', '-0.5684', '0.05795', '0.628', '-0.54']",C168729,,C567430,,,,
mondo:0012790,amyotrophic lateral sclerosis type 10,"['amyotrophic lateral sclerosis caused by mutation in TARDBP', 'frontotemporal lobar Degeneration with Tdp43 inclusions, Tardbp-related', 'frontotemporal lobar degeneration, TARDBP-related', 'amyotrophic lateral sclerosis 10, with or without frontotemporal dementia', 'amyotrophic lateral sclerosis 10', 'ALS10', 'frontotemporal dementia with Tdp43 inclusions, Tardbp-related', 'amyotrophic lateral sclerosis 10 with or without frontotemporal dementia', 'amyotrophic lateral sclerosis 10, with or without FTD', 'Ftld-TDP, Tardbp-related', 'TARDBP amyotrophic lateral sclerosis', 'TARDBP-related frontotemporal lobar degeneration with Tdp43 inclusions']",0060201,612069,,C3502417,,,,C567429,,,,
mondo:0012791,"mitochondrial DNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria","['booth-Haworth-Dilling syndrome', 'mitochondrial dna depletion syndrome, encephalomyopathic form with methylmalonic aciduria, autosomal recessive', 'mitochondrial encephalomyopathy aminoacidopathy', 'mitochondrial encephalomyopathy-aminoacidopathy syndrome', 'mtDNA depletion syndrome, encephalomyopathic form with methylmalonic aciduria', 'mitochondrial DNA depletion syndrome 5', 'MTDPS5', 'mitochondrial DNA depletion syndrome 5 (encephalomyopathic with or without methylmalonic aciduria)', 'mitochondrial DNA depletion syndrome, encephalomyopathic form, with or without methylmalonic aciduria, autosomal recessive, Sucla2-related', 'encephalomyopathy', 'mitochondrial DNA depletion syndrome type 5']",0080124,612073,1933,,"['-0.4866', '0.2808', '-0.012184', '-0.05255', '-0.0636', '-0.4744', '-0.3403', '0.6616', '-0.01804', '0.3137', '-0.3242', '-0.5537', '0.07214', '-0.3608', '-0.003649', '-0.1306', '-0.0209', '-0.03677', '-0.615', '-0.733', '0.2876', '-0.4429', '0.1808', '-0.1744', '0.403', '-0.164', '-0.1893', '0.03302', '-0.15', '-0.01819', '0.05487', '0.1245', '0.527', '-0.3025', '-0.0745', '-0.1395', '-0.5186', '-0.2355', '-0.09717', '-0.0931', '0.2517', '-0.5933', '-0.008575', '0.2394', '-0.2161', '-0.359', '-0.2175', '-0.1653', '-0.2449', '-0.2375', '-0.2607', '0.1221', '-0.03635', '-0.1022', '0.1262', '-0.2322', '0.4907', '-0.2433', '-0.4863', '0.5566', '0.2725', '-0.2708', '0.489', '-0.04385', '-0.7407', '0.04453', '0.2344', '0.407', '-0.5234', '0.611', '-0.2472', '0.527', '0.11566', '0.3416', '-0.11017', '0.08295', '0.2352', '-0.1008', '-0.191', '0.3853', '0.5044', '0.2185', '0.000761', '0.2008', '0.09015', '0.2751', '0.2585', '0.4575', '0.2812', '0.2372', '0.759', '0.1549', '-0.1698', '0.00769', '0.1312', '0.3555', '0.2542', '-0.11743', '-0.1508', '-0.1458']",,,C567624,,,,
mondo:0012792,mitochondrial DNA depletion syndrome 8a,"['mitochondrial DNA depletion syndrome, encephalomyopathic, with renal tubulopathy, autosomal recessive', 'mitochondrial neurogastrointestinal encephalopathy syndrome, Rrm2B-related', 'encephalomyopathic type with renal tubulopathy', 'mitochondrial DNA depletion syndrome caused by mutation in RRM2B', 'RRM2B mitochondrial DNA depletion syndrome', 'mtDNA depletion syndrome, encephalomyopathic form with renal tubulopathy', 'mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)', 'mitochondrial DNA depletion syndrome 8B (Mngie type)', 'mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy', 'mitochondrial DNA depletion syndrome type 8a', 'Mngie, Rrm2B-related', 'MTDPS8A', 'RRM2B-related mitochondrial DNA depletion syndrome']",0080127,612075,298,,"['-0.559', '0.2183', '-0.01076', '0.2842', '-0.1655', '-0.5703', '-0.03516', '0.3477', '-0.3643', '-0.06995', '-0.2133', '-0.4624', '-0.211', '0.2241', '-0.1954', '-0.2167', '-0.09674', '-0.02626', '-0.0825', '-0.7676', '0.2126', '-0.3608', '0.02443', '0.1438', '0.501', '0.1088', '-0.3503', '0.172', '-0.2035', '0.3755', '0.00812', '-0.04938', '0.5093', '0.004', '0.1877', '-0.3833', '-0.1833', '-0.10175', '-0.4226', '0.1298', '-0.2751', '-0.01808', '-0.1105', '0.2307', '-0.655', '-0.3198', '-0.2666', '-0.664', '0.2683', '0.506', '-0.49', '0.04144', '0.005848', '-0.05322', '0.202', '-0.4348', '0.2408', '0.616', '-0.1567', '0.2474', '0.0578', '0.2522', '0.35', '-0.04617', '0.03857', '0.1472', '-0.008705', '0.4473', '-0.48', '0.4004', '-0.462', '0.2004', '-0.01987', '0.276', '0.0785', '-0.05554', '0.4236', '-0.304', '-0.1443', '0.285', '0.1907', '0.236', '-0.2191', '0.1646', '0.2268', '0.1289', '0.5044', '0.257', '0.503', '0.629', '0.4414', '0.04123', '-0.3062', '-0.04175', '0.1416', '0.742', '0.2847', '-0.414', '0.4092', '0.2017']",,,,,,,
mondo:0012793,"hypouricemia, renal, 2","['uric acid concentration, serum, quantitative trait locus 2', 'gout susceptibility 2', 'hypouricemia, renal, type 2', 'hypouricemia, renal, 2', 'uric acid concentration, serum, QTL 2', 'RHUC2']",,612076,,C2677549,,,,C567426,,,,
mondo:0012794,ANE syndrome,"['ANE syndrome', 'anes', 'alopecia-progressive neurological defect-endocrinopathy syndrome', 'alopecia, neurologic defects, and endocrinopathy syndrome']",0112244,612079,157954,C2677535,"['-1.454', '0.0935', '0.3154', '-0.5737', '0.4094', '-0.3115', '-0.1667', '0.2876', '-1.033', '0.013626', '-0.293', '0.0647', '-0.2666', '-0.1467', '-0.04803', '-0.3486', '0.634', '-0.1392', '-0.7305', '-0.8823', '0.1816', '-0.194', '0.1597', '-0.176', '0.3035', '0.2732', '-0.1364', '-0.3643', '-0.10956', '-0.782', '0.4207', '0.3333', '0.342', '0.1116', '0.04932', '-0.3948', '-0.813', '-0.0892', '-0.3389', '-0.1417', '0.467', '0.455', '-0.11334', '0.711', '0.2588', '-0.8174', '0.3135', '-0.10425', '-0.006153', '-0.03925', '0.1122', '-0.007607', '-0.1642', '0.4695', '-0.7246', '0.1862', '0.296', '-0.4744', '-0.1603', '0.2191', '0.3262', '0.1049', '0.1368', '0.04083', '-0.06836', '0.547', '0.4294', '1.104', '-0.1351', '-0.0222', '-0.6743', '-0.1895', '0.581', '-0.1803', '-0.1565', '-0.4082', '0.06076', '0.08264', '0.1307', '-0.0835', '0.2045', '-0.3572', '-0.4702', '0.2404', '0.10284', '-0.0882', '-0.0835', '0.1125', '0.889', '0.173', '0.451', '0.6025', '0.1761', '-0.5317', '1.15', '-0.2937', '0.7007', '-0.005066', '0.8394', '0.2426']",,,C567425,,,,
mondo:0012795,hypophosphatemic rickets and hyperparathyroidism,['hypophosphatemic rickets and hyperparathyroidism'],,612089,,C2677524,,,,C567423,,,,
mondo:0012796,retinitis pigmentosa 41,"['retinitis pigmentosa caused by mutation in PROM1', 'retinitis pigmentosa 41', 'RP 41', 'retinitis pigmentosa type 41', 'PROM1 retinitis pigmentosa', 'retinal Degeneration, autosomal recessive, prominin-related', 'RP41']",0110376,612095,,C2677516,,,,C567422,,H35.5,,
mondo:0012797,otosclerosis 8,"['OTSC8', 'otosclerosis 8']",,612096,,C2677515,,,,C567421,,,,
mondo:0012798,"deafness, unilateral, with delayed endolymphatic hydrops","['deafness, unilateral, with delayed endolymphatic hydrops']",,612097,,C2677512,,,,C567420,,,,
mondo:0012799,hypertrophic cardiomyopathy 11,"['cardiomyopathy, familial hypertrophic, 11', 'CMH11', 'cardiomyopathy, familial hypertrophic, type 11', 'cardiomyopathy, hypertrophic, 11', 'cardiomyopathy familial hypertrophic 11', 'hypertrophic cardiomyopathy caused by mutation in ACTC1', 'ACTC1 hypertrophic cardiomyopathy', 'hypertrophic cardiomyopathy type 11']",0110317,612098,,C2677506,,,,C567419,,,,
mondo:0012800,"trichoepithelioma, multiple familial, 2","['trichoepithelioma, multiple familial, type 2', 'trichoepithelioma multiple familial 2', 'Mft2', 'multiple familial trichoepithelioma 2', 'trichoepithelioma, multiple familial, 2']",,612099,,C2677505,,,,C567418,,,,
mondo:0012801,"autism, susceptibility to, 15","['autism, susceptibility to, 15', 'autism susceptibility 15', 'AUTS15', 'autism, susceptibility to, type 15', 'susceptibility to autism 15']",,612100,,,,,,,,,,
mondo:0012802,oculoauricular syndrome,"['oculoauricular syndrome', 'OCACS', 'oculoauricular syndrome, Schorderet type', 'microphthalmia, microcornea, anterior segment dysgenesis, cataract, ocular coloboma, retinal pigment epithelium abnormalities, Rod-cone dystrophy, and anomalies of the external Ear', 'Schorderet-Munier-Franceschetti syndrome']",0060482,612109,157962,C2677500,"['-0.2415', '-0.0673', '0.5703', '-0.2642', '0.2603', '-0.61', '0.1603', '0.2703', '-0.549', '-0.05682', '-0.4258', '-0.502', '0.1721', '-0.1037', '-0.675', '-0.2194', '0.562', '-0.3042', '0.04962', '-0.6143', '-0.1006', '0.05902', '0.10974', '-0.013756', '0.05283', '-0.1982', '-0.516', '0.1523', '0.3115', '-0.4614', '0.3892', '0.3467', '0.5015', '0.119', '0.3794', '-0.1598', '0.2922', '0.0698', '-0.2126', '-1.037', '0.394', '0.1497', '0.0442', '0.1681', '-0.31', '-0.4194', '0.466', '0.5884', '0.1918', '-0.0939', '-0.2106', '0.0044', '-0.099', '-0.2014', '-0.2976', '-0.4866', '0.435', '0.03087', '-0.353', '0.095', '-0.0622', '0.05707', '-0.0966', '0.509', '0.01735', '-0.0706', '0.6606', '0.565', '-0.1304', '0.1791', '-0.1782', '0.5', '0.3398', '0.139', '-0.1531', '-0.1348', '-0.003433', '-0.2039', '-0.883', '0.1525', '0.1951', '0.2437', '-0.2322', '0.605', '-0.0764', '-0.4275', '-0.0669', '0.463', '0.02957', '0.1666', '0.004444', '0.523', '0.4404', '0.2668', '0.567', '-0.506', '0.809', '-0.2625', '-0.0432', '0.1547']",,,C567416,,,,
mondo:0012803,diarrhea-vomiting due to trehalase deficiency,"['trehalose intolerance', 'trehalase deficiency', 'isolated trehalose intolerance']",,612119,103909,C0268187,"['0.215', '-0.01089', '0.6147', '0.4143', '-0.4827', '-0.8203', '-0.8467', '0.4453', '-0.01174', '-0.00822', '0.6167', '0.8394', '0.2449', '0.669', '-1.0', '0.1686', '-0.4177', '0.09204', '-0.7085', '-0.878', '0.05438', '-0.359', '-0.1432', '-0.236', '-0.008644', '-0.699', '-0.8687', '0.3542', '0.4116', '-0.9014', '-0.4324', '-0.531', '-0.1785', '0.493', '0.8867', '0.4575', '-0.4607', '0.4724', '0.184', '-0.0964', '-0.575', '-0.6206', '-0.2842', '-0.6636', '0.4365', '-0.003784', '0.1393', '0.1722', '0.2023', '1.052', '-0.754', '-0.0287', '0.04572', '-0.1172', '0.0743', '-0.3147', '-0.1709', '0.11084', '-0.796', '-0.1143', '0.4873', '0.743', '0.516', '-0.3752', '0.122', '-0.03088', '0.3032', '-0.363', '0.2573', '1.098', '-0.3691', '0.7593', '0.2056', '-0.787', '0.714', '0.457', '-0.7686', '0.3293', '0.03204', '0.565', '-0.243', '-0.7075', '-0.2429', '-0.0453', '0.356', '0.3218', '0.552', '0.05118', '0.1605', '-0.3135', '-0.2195', '-0.313', '-0.265', '-0.2935', '0.706', '0.74', '0.2712', '-1.966', '-0.1255', '-0.4758']",,,C562603,271.8,,,
mondo:0012804,hypertrophic cardiomyopathy 12,"['cardiomyopathy, hypertrophic, 12', 'cardiomyopathy, familial hypertrophic, 12', 'hypertrophic cardiomyopathy type 12', 'cardiomyopathy familial hypertrophic 12', 'CMH12', 'CSRP3 hypertrophic cardiomyopathy', 'cardiomyopathy, familial hypertrophic, type 12', 'hypertrophic cardiomyopathy caused by mutation in CSRP3']",0110318,612124,,C2677491,,,,,,,,
mondo:0012805,childhood onset GLUT1 deficiency syndrome 2,"['paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anaemia', 'DYT18', 'PxMD-SLC2A1', 'GLUT1 deficiency syndrome 2', 'dystonia 18', 'GLUT1DS2', 'paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic Anemia', 'ped with or without epilepsy and/or hemolytic Anaemia', 'DYT-SLC2A1', 'ped with or without epilepsy and/or hemolytic Anemia', 'GLUT1 deficiency syndrome type 2', 'GLUT1 deficiency syndrome 2, childhood onset', 'paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anemia', 'ped', 'paroxysmal exertion-induced dyskinesia', 'paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic Anaemia', 'paroxysmal exercise-induced dystonia', 'childhood onset GLUT1 deficiency syndrome type 2']",0090045,612126,98811,C1842534,"['0.4038', '0.328', '-0.5874', '-0.28', '-0.11694', '-0.8965', '0.887', '0.389', '-0.4766', '-0.229', '-0.4028', '0.10144', '-0.2119', '-0.1519', '0.751', '0.679', '0.2256', '-0.2693', '-0.2299', '-0.803', '0.1592', '-0.012276', '0.02255', '-0.284', '-0.3242', '0.176', '-0.5396', '0.03052', '-0.23', '-0.2091', '0.0818', '0.529', '0.542', '-0.07513', '-0.3254', '-0.4917', '-0.2286', '-0.383', '-0.11896', '0.2451', '0.9004', '-0.976', '0.349', '-0.11847', '0.5986', '-0.105', '-0.5312', '0.517', '0.342', '0.847', '-0.3726', '0.0956', '-0.02594', '-0.179', '0.0667', '-0.06354', '0.79', '-0.8345', '-0.1998', '0.2815', '-0.2908', '-0.006866', '0.06305', '-0.4143', '-0.3496', '0.201', '0.2402', '0.3003', '-0.006874', '0.5186', '0.1223', '0.2366', '0.1971', '-0.6055', '0.645', '1.065', '0.1503', '0.2556', '-0.402', '0.2625', '0.4282', '0.39', '0.5815', '0.0708', '0.522', '0.3552', '-0.3718', '0.422', '0.2314', '0.7603', '0.805', '0.03632', '-0.003534', '0.1558', '0.3105', '0.2035', '0.561', '-0.444', '-0.4116', '-0.5835']",,,C564288,,,,
mondo:0012806,ectodermal dysplasia and immunodeficiency 2,"['ectodermal dysplasia, anhidrotic, with T-cell immunodeficiency, autosomal dominant', 'EPAID2']",0081079,612132,,C2677481,,C176826,,C567411,,,,
mondo:0012807,"epidermolysis bullosa simplex 5C, with pyloric atresia","['epidermolysis bullosa simplex 5C, with pyloric atresia', 'epidermolysis bullosa simplex with pyloric atresia', 'EBSPA', 'EBS with pyloric atresia', 'EBS-PA']",,612138,158684,C2677349,"['0.6763', '-0.3076', '-0.2644', '-0.1415', '-0.0698', '-0.7153', '-0.599', '0.4514', '-0.0656', '-0.5835', '0.2979', '-0.56', '-1.027', '0.404', '-0.9165', '0.3289', '0.10297', '-1.039', '-0.4104', '-0.9526', '-0.1534', '-0.183', '0.4497', '0.436', '0.5264', '0.1048', '-0.9116', '0.837', '-0.1837', '-0.7124', '0.2048', '0.01497', '-0.0585', '0.1001', '0.03387', '0.1357', '-1.082', '0.2144', '1.084', '-0.5195', '0.1941', '-0.637', '0.1272', '0.0447', '0.04666', '-0.3145', '-0.382', '0.06635', '0.461', '-0.1418', '-0.717', '-0.775', '0.5435', '-0.07214', '-0.02626', '-0.607', '-0.3582', '1.244', '-0.65', '-0.2214', '-0.1862', '0.5083', '0.12463', '0.3884', '0.9277', '0.8403', '0.3955', '0.2593', '-0.641', '0.2607', '-0.1186', '0.0915', '-0.386', '-0.10956', '-0.09827', '-0.1888', '0.10974', '-0.001078', '-0.01324', '-0.3606', '-0.97', '0.06586', '-0.355', '-0.2537', '0.10077', '0.3132', '-1.009', '0.694', '1.103', '0.1947', '-0.4578', '0.4941', '-0.0719', '0.4875', '-0.0732', '0.7344', '0.1719', '-0.5977', '0.918', '0.1549']",,,C567408,,,,
mondo:0012808,dilated cardiomyopathy 1AA,"['familial isolated dilated cardiomyopathy caused by mutation in ACTN2', 'cardiomyopathy, dilated, 1AA, with or without left ventricular noncompaction', 'dilated cardiomyopathy 1AA with or without left ventricular noncompaction', 'cardiomyopathy, hypertrophic, 23, with or without LVNC', 'CMD1AA', 'cardiomyopathy, familial hypertrophic, 23, with or without ventricular noncompaction', 'cardiomyopathy, dilated, 1AA, with or without LVNC', 'dilated cardiomyopathy type 1AA', 'ACTN2 familial isolated dilated cardiomyopathy']",0110428,612158,,C2677338,,,,C567407,,,,
mondo:0012809,"histiocytoma, Angiomatoid fibrous","['angiomatoid fibrous histiocytoma', 'angiomatoid malignant fibrous histiocytoma', 'AFH', 'histiocytoma, Angiomatoid fibrous', 'histiocytoma, angiomatoid fibrous, somatic']",,612160,569164,C1266127,,C6494,,C563181,,,,
mondo:0012810,"aneurysm, intracranial berry, 7","['ANIB7', 'aneurysm, intracranial BERRY, 7']",0080970,612161,,C2677337,,,,C567406,,,,
mondo:0012811,"aneurysm, intracranial berry, 8","['aneurysm, intracranial BERRY, 8', 'ANIB8']",0080971,612162,,C2677336,,,,C567405,,,,
mondo:0012812,"developmental and epileptic encephalopathy, 4","['STXBP1-related early-onset encephalopathy', 'STXBP1-related encephalopathy', 'early infantile epileptic encephalopathy caused by mutation in STXBP1', 'epileptic encephalopathy, early infantile, type 4', 'EIEE4', 'DEE4', 'developmental and epileptic encephalopathy 4', 'STXBP1 early infantile epileptic encephalopathy', 'early infantile epileptic encephalopathy 4', 'epileptic encephalopathy, early infantile, 4']",0080436,612164,599373,C2677326,"['0.7676', '-0.06903', '-0.2', '0.1355', '-0.92', '-0.2578', '0.8916', '0.931', '-0.2024', '-0.08276', '-0.749', '0.01915', '0.4856', '0.305', '0.2605', '-0.3945', '-0.05072', '-0.7427', '0.2003', '-1.027', '0.3718', '0.2', '0.3083', '0.10596', '0.11115', '-0.00225', '-0.2043', '-0.335', '-0.9175', '0.00789', '0.5503', '0.3325', '0.1223', '0.1481', '-0.01668', '0.1611', '0.0924', '-0.2037', '-0.22', '-0.3652', '0.0787', '-0.6807', '0.519', '-0.01503', '-0.02315', '-0.0317', '-0.4602', '-0.0036', '0.2019', '0.7485', '-0.4546', '0.04565', '-0.1339', '-0.2407', '0.2184', '0.04877', '0.495', '0.2006', '-0.2915', '0.1329', '-0.334', '0.417', '0.317', '-0.10803', '0.1699', '0.3105', '0.0806', '0.0005183', '0.4624', '0.679', '0.01297', '0.6665', '0.2896', '0.00363', '-0.3735', '0.05817', '0.3206', '-0.3877', '-0.573', '-0.1114', '0.3384', '0.5396', '-0.2642', '0.6016', '-0.1051', '-0.0225', '0.2363', '0.2905', '0.6973', '0.4138', '0.05368', '0.2426', '0.0619', '0.1447', '-0.1475', '0.1265', '0.7124', '-0.378', '0.07574', '-0.4722']",C162472,,C567404,,,,
mondo:0012813,retinitis pigmentosa 29,"['RP29', 'RP 29', 'retinitis pigmentosa type 29', 'retinitis pigmentosa 29']",0110378,612165,,C2677325,,,,C567403,,H35.5,,
mondo:0012814,diastasis recti and weakness of the linea alba,['diastasis recti and weakness of the linea alba'],,612198,,C2677303,,,,C567402,,,,
mondo:0012815,Coats plus syndrome,"['cerebroretinal microangiopathy with calcfications and cysts', 'cerebroretinal microangiopathy with calcifications and cysts', 'CRMCC']",,,313838,CN282828,"['-0.2141', '0.1125', '0.185', '-0.3557', '0.1296', '-0.3306', '0.0183', '0.02658', '-0.1298', '0.0393', '-0.1959', '-0.004864', '0.0653', '-0.267', '0.010086', '-0.3816', '-0.09216', '0.2927', '0.04822', '-0.3284', '-0.0972', '-0.3044', '0.0804', '-0.3213', '0.015045', '-0.1399', '-0.0806', '-0.1004', '0.1292', '-0.1603', '0.02487', '0.1754', '0.081', '-0.0543', '0.0752', '-0.07947', '-0.0679', '-0.2148', '0.02724', '-0.525', '-0.033', '-0.1361', '0.386', '-0.1547', '0.104', '-0.3362', '-0.1718', '0.1624', '0.079', '-0.345', '0.0097', '0.2151', '0.1627', '0.1371', '-0.01458', '-0.2188', '0.2761', '-0.002352', '-0.3477', '0.3003', '0.3923', '0.1937', '0.073', '-0.1744', '0.0803', '-0.2067', '0.3289', '0.282', '-0.2732', '0.5024', '-0.1605', '-0.1975', '-0.01095', '-0.0689', '-0.1968', '-0.1405', '0.1439', '0.1456', '0.1758', '-0.1498', '-0.1307', '0.0787', '-0.00978', '0.3157', '-0.34', '0.08575', '0.4749', '0.1462', '-0.1715', '-0.04657', '0.1729', '0.399', '-0.0453', '0.02522', '0.5996', '0.4746', '0.6914', '-0.2408', '0.0646', '0.02638']",,,C567401,348.89,,,
mondo:0012816,"atrial fibrillation, familial, 6","['NPPA familial atrial fibrillation', 'ATFB6', 'familial atrial fibrillation caused by mutation in NPPA', 'atrial fibrillation, familial, 6', 'atrial fibrillation, familial, type 6']",,612201,,C2677294,,,,C567400,,,,
mondo:0012817,Ewing sarcoma,"['ES', 'Ewing tumor', 'localised Ewing sarcoma', 'localized Ewing sarcoma', 'Ewing^s tumor', 'Ewing sarcoma', 'localised Ewing^s sarcoma/peripheral primitive neuroectodermal tumour', 'localized Ewing^s tumor', 'localized Ewing^s sarcoma', 'neuroepithelioma', 'Ewings sarcoma-primitive neuroectodermal tumor', 'localised peripheral primitive neuroectodermal tumour', 'peripheral primitive neuroectodermal tumour', 'sarcoma, Ewing^s', 'Ewing^s tumour', 'localised Ewing^s tumour', 'localized peripheral primitive neuroectodermal tumor', 'localized Ewing^s sarcoma/peripheral primitive neuroectodermal tumor', 'PNET of Thoracopulmonary region', 'Ewing^s sarcoma', 'Ewing^s sarcoma/peripheral primitive neuroectodermal tumour', 'neuroepithelioma, peripheral', 'localised Ewing^s sarcoma', 'Ewing tumour', 'Ewing^s family localized tumor', 'Ewings sarcoma-primitive neuroectodermal tumour', 'Ewings sarcoma', 'Ewing^s family localised tumour']",3369,612219,319,C3489398,"['-0.02788', '0.282', '0.1913', '-0.0716', '0.432', '-0.317', '0.334', '0.686', '-0.5938', '-0.578', '0.0361', '0.4524', '0.1251', '0.4536', '-0.0787', '-0.09515', '-0.567', '-0.7183', '-0.2101', '-0.676', '0.2062', '-0.3274', '0.8726', '-0.389', '-0.1418', '-0.1444', '-0.1735', '0.2517', '-0.599', '-0.0681', '-0.00398', '-0.108', '0.7856', '-0.506', '0.1179', '-0.1964', '-1.038', '-0.3794', '-0.2003', '-0.2327', '0.3025', '-0.02242', '0.1775', '-0.568', '0.8223', '0.396', '-0.942', '-0.36', '0.859', '0.02895', '0.486', '-0.5586', '0.3274', '-0.009094', '0.1351', '0.0416', '-0.8525', '0.4502', '-0.11176', '-0.1672', '0.3816', '0.4263', '-0.586', '-0.1233', '-0.3716', '0.3987', '0.02025', '-0.1381', '0.02406', '1.073', '0.4836', '0.4565', '0.3335', '-0.04807', '0.5044', '0.2808', '-0.3806', '0.02489', '-0.193', '-1.206', '-0.1581', '-0.328', '0.0839', '0.1016', '-0.3608', '-0.8184', '0.3643', '0.4214', '0.136', '-0.3022', '0.0004337', '-0.663', '-0.615', '-0.4553', '0.622', '-0.2235', '-0.003986', '-0.7383', '0.1749', '-0.3674']",C9341,0000174,D012512,,C40.3,10015560,
mondo:0012818,maturity-onset diabetes of the young type 9,"['MODY9', 'PAX4 maturity-onset diabetes of the young (disease)', 'diabetes mellitus MODY type 9', 'MODY type 9', 'maturity-onset diabetes of the young, type IX', 'maturity-onset diabetes of the young, type 9', 'MODY PAX4 related', 'type 9 maturity-onset diabetes of the young']",0111107,612225,,C2677132,,,,C567393,,,,
mondo:0012819,diabetic ketoacidosis,"['ketosis-prone diabetes mellitus', 'KPD']",1837,,,C0011880,"['0.08997', '0.2673', '-0.2712', '0.4194', '-0.1572', '-0.3447', '0.1829', '0.9814', '-0.4844', '-0.1332', '-0.1454', '-0.145', '0.409', '1.058', '-0.618', '-0.04553', '-0.163', '0.267', '-0.11053', '-0.6377', '0.05093', '-0.000612', '0.264', '-0.0712', '-0.692', '-0.6455', '-0.1056', '0.1171', '0.1033', '-0.2173', '0.1482', '0.02103', '-0.04596', '-0.156', '-0.4165', '0.5713', '-0.527', '0.9272', '0.4717', '-0.3135', '-0.09973', '-0.541', '0.1123', '-0.2979', '0.2822', '-0.08014', '-0.2483', '-0.09705', '-0.3079', '0.461', '-0.11664', '0.02426', '0.9155', '-0.6743', '-0.1647', '0.68', '0.2053', '-0.5386', '-0.7583', '0.1576', '-0.472', '0.2654', '-0.2181', '-0.4058', '-0.5474', '0.4866', '0.1226', '-0.4636', '-1.007', '0.1045', '0.0085', '0.3796', '-0.321', '-0.7017', '0.2349', '0.6846', '0.29', '0.556', '0.2164', '0.05777', '0.3293', '-0.1218', '-0.506', '0.1617', '0.08594', '0.2888', '-0.3584', '-0.2161', '0.54', '0.1511', '0.1863', '0.1646', '-0.165', '-0.0728', '0.2717', '0.822', '-0.3225', '-0.4902', '-0.9746', '0.484']",,1000897,D016883,250.10,,10012671,
mondo:0012820,"colorectal cancer, susceptibility to, 3","['colorectal cancer caused by mutation in SMAD7', 'SMAD7 colorectal cancer', 'colorectal cancer, susceptibility to, on chromosome 18', 'colorectal cancer, susceptibility to, 3', 'susceptibility to colorectal cancer 3', 'CRCS3', 'colorectal cancer, susceptibility to, type 3']",,612229,,,,,,,,,,
mondo:0012821,"colorectal cancer, susceptibility to, 5","['colorectal cancer, susceptibility to, 5', 'CRCS5', 'colorectal cancer, susceptibility to, on chromosome 10']",,612230,,,,,,,,,,
mondo:0012822,"colorectal cancer, susceptibility to, 6","['colorectal cancer, susceptibility to, on chromosome 8Q23', 'colorectal cancer, susceptibility to, 6', 'CRCS6']",,612231,,,,,,,,,,
mondo:0012823,"colorectal cancer, susceptibility to, 7","['colorectal cancer, susceptibility to, on chromosome 11', 'colorectal cancer, susceptibility to, 7', 'CRCS7']",,612232,,,,,,,,,,
mondo:0012824,hypomyelinating leukodystrophy 4,"['MitCHAP60 disease', 'leukodystrophy, hypomyelinating, type 4', 'leukodystrophy caused by mutation in HSPD1', 'hypomyelinating leukodystrophy type 4', 'Mitchap60 disease', 'Pelizaeus-Merzbacher-like disease due to HSPD1 mutation', 'leukodystrophy, hypomyelinating, 4', 'mitochondrial Hsp60 chaperonopathy', 'HSPD1 leukodystrophy', 'mitochondrial HSP60 chaperonopathy', 'HLD4']",0060789,612233,280288,C2677109,"['-0.2588', '0.2253', '0.002428', '0.02094', '0.0594', '-0.2944', '-0.1154', '0.125', '-0.327', '-0.04977', '-0.0419', '0.01718', '-0.06204', '-0.04352', '0.2087', '-0.1963', '-0.067', '-0.097', '-0.10016', '-0.2441', '0.1477', '-0.1224', '0.0621', '-0.00633', '0.1138', '-0.02916', '-0.01527', '0.0517', '0.01999', '-0.0553', '0.07684', '0.0628', '0.2083', '0.02644', '0.1635', '-0.1404', '0.004696', '-0.0551', '0.07623', '-0.207', '0.1072', '-0.185', '0.09753', '0.02287', '-0.1267', '-0.226', '0.03595', '0.0678', '0.139', '-0.013', '0.0308', '-0.06195', '-0.009926', '0.0077', '-0.1129', '-0.1676', '0.342', '0.06146', '-0.2615', '0.1279', '0.0464', '0.1554', '0.1799', '-0.00931', '0.0939', '0.1642', '0.1697', '0.0589', '-0.173', '0.1182', '-0.2245', '0.02156', '0.07166', '-0.1752', '0.10297', '0.03714', '0.0755', '0.1046', '-0.1421', '0.01084', '-0.05487', '-0.061', '-0.09', '0.1099', '-0.01692', '-0.1484', '0.179', '0.2866', '0.2345', '0.1549', '0.0625', '0.001685', '-0.006924', '-0.1109', '0.4216', '0.1578', '0.2515', '-0.2935', '0.0004435', '-0.01261']",,,C567390,,,,
mondo:0012825,extraskeletal myxoid chondrosarcoma,"['extraskeletal chondrosarcoma', 'myxoid extraosseous chondrosarcoma', 'EMC', 'chondrosarcoma, extraskeletal myxoid', 'extraosseous chondrosarcoma', 'myxoid extraskeletal chondrosarcoma']",6496,612237,209916,C1275278,,C27502,,C563195,171.9,,,
mondo:0012826,"scoliosis, isolated, susceptibility to, 4","['scoliosis, idiopathic, susceptibility to, 4', 'IS4', 'scoliosis, isolated, susceptibility to, 4']",,612238,,,,,,,,,,
mondo:0012827,"scoliosis, isolated, susceptibility to, 5","['IS5', 'scoliosis, idiopathic, susceptibility to, 5', 'scoliosis, isolated, susceptibility to, 5']",,612239,,,,,,,,,,
mondo:0012828,"atrial fibrillation, familial, 7","['atrial fibrillation, familial, type 7', 'KCNA5 familial atrial fibrillation', 'familial atrial fibrillation caused by mutation in KCNA5', 'ATFB7', 'atrial fibrillation, familial, 7']",,612240,,C2677106,,,,C567389,,,,
mondo:0012829,inflammatory bowel disease 12,"['inflammatory bowel disease type 12', 'IBD12', 'inflammatory bowel disease 12']",0110887,612241,,C2677105,,,,C567388,,,,
mondo:0012830,chromosome 10q23 deletion syndrome,"['chromosome 10q23 deletion syndrome', 'juvenile polyposis, infantile', '10q22.3q23.3 microdeletion syndrome', '10q22.3q23 microdeletion syndrome', 'juvenile polyposis of infancy', 'chromosome 10Q22.3-q23.2 deletion syndrome', 'deletion 10q22.3q23.3', 'Del(10)(q22.3q23.3)', 'monosomy 10q22.3q23.3', 'chromosome 10q22.3-q23.2 deletion syndrome']",0060389,612242,79076,CN202618,"['0.02415', '0.09155', '-0.5156', '-0.0787', '-0.1942', '-0.1729', '0.05127', '0.7495', '-0.821', '0.1021', '-0.3752', '0.0951', '-0.3682', '0.0529', '-0.4644', '-0.08496', '-0.403', '-0.3804', '-0.2744', '-0.3928', '0.3657', '0.1868', '0.814', '-0.64', '0.353', '0.569', '0.2803', '0.2917', '0.299', '-0.4685', '0.506', '-0.3848', '-0.02596', '-0.1123', '0.2585', '0.5073', '-0.806', '-0.2937', '-0.4631', '0.4934', '0.377', '-0.632', '0.4463', '-0.567', '0.3757', '0.1516', '-0.46', '-0.1521', '-0.09375', '0.0159', '-0.3118', '-0.1564', '-0.2197', '-0.435', '-0.246', '-0.1945', '-0.2029', '0.3823', '-0.7163', '-0.2186', '0.1906', '0.122', '0.1459', '0.01473', '0.2473', '0.3525', '0.7344', '-0.1498', '-0.04147', '0.2612', '0.1534', '-0.214', '-0.2878', '-0.3306', '0.03745', '-0.2537', '0.4072', '-0.05646', '0.2922', '-0.1848', '-0.1857', '-0.00855', '-0.11444', '0.0751', '0.183', '-0.1631', '0.391', '0.1464', '0.3523', '-0.588', '0.01952', '-0.1624', '-0.3435', '-0.173', '0.7935', '-0.1084', '0.356', '-0.418', '-0.436', '0.07367']",,,C567385,,,,
mondo:0012831,inflammatory bowel disease 13,"['ABCB1 inflammatory bowel disease', 'inflammatory bowel disease caused by mutation in ABCB1', 'inflammatory bowel disease 13', 'inflammatory bowel disease type 13', 'IBD13']",0110893,612244,,C2677101,,,,C567384,,,,
mondo:0012832,inflammatory bowel disease 14,"['inflammatory bowel disease type 14', 'inflammatory bowel disease 14', 'IRF5 inflammatory bowel disease', 'IBD14', 'inflammatory bowel disease caused by mutation in IRF5']",0110895,612245,,C2677100,,,,C567383,,,,
mondo:0012833,Crouzon syndrome-acanthosis nigricans syndrome,"['can', 'Crouzon syndrome with acanthosis nigricans', 'Crouzon-dermoskeletal syndrome', 'Crouzonodermoskeletal syndrome', 'CAN', 'Chronic kidney allograft nephropathy', 'chronic allograft nephropathy']",0111161,612247,93262,,"['0.4517', '0.4412', '-0.2411', '-0.1887', '0.336', '-0.5254', '-0.616', '0.3486', '-0.3965', '-0.844', '-0.1786', '0.12274', '-0.7324', '-0.11346', '-0.3354', '-0.3242', '-0.3286', '-0.0926', '-0.03757', '-0.7783', '0.287', '-0.4934', '-0.305', '-0.4236', '0.3933', '0.5767', '-0.3992', '-0.3315', '0.9067', '-0.4954', '0.9155', '-0.2278', '0.3325', '-0.763', '0.3162', '0.3872', '-0.6724', '0.2766', '0.05652', '-0.1638', '0.1061', '-0.0562', '-0.02972', '-0.5757', '0.0647', '-0.12354', '-0.1444', '0.01261', '-0.2815', '-0.0107', '0.09314', '0.4346', '0.465', '-0.0946', '-0.0858', '0.2073', '-0.3025', '0.01854', '-0.0946', '-0.2693', '0.2269', '-0.348', '-0.4287', '-0.04453', '-0.2634', '-0.1741', '0.2842', '0.156', '-0.566', '0.9253', '0.03558', '0.4746', '0.3806', '-0.1676', '-0.1334', '0.4', '0.1643', '0.03964', '-0.3625', '-0.6514', '0.3604', '0.2883', '0.01952', '-0.4817', '-0.7007', '0.5522', '-0.00777', '-0.2404', '0.3682', '0.178', '0.2379', '0.127', '0.473', '0.1649', '0.3613', '-0.604', '0.3508', '0.2988', '0.0638', '0.1603']",C38145,,C567382,,,,
mondo:0012834,"systemic lupus erythematosus, susceptibility to, 10","['susceptibility to systemic lupus erythematosus 10', 'SLEB10', 'systemic lupus erythematosus, susceptibility to, 10', 'systemic lupus erythematosus, susceptibility to, type 10', 'IRF5 systemic lupus erythematosus (disease)']",,612251,,,,,,,,,,
mondo:0012835,"systemic lupus erythematosus, susceptibility to, 11","['systemic lupus erythematosus, susceptibility to, 11', 'SLEB11', 'susceptibility to systemic lupus erythematosus 11', 'systemic lupus erythematosus, susceptibility to, type 11', 'STAT4 systemic lupus erythematosus (disease)']",,612253,,,,,,,,,,
mondo:0012836,"systemic lupus erythematosus, susceptibility to, 12","['systemic lupus erythematosus, susceptibility to, 12', 'SLEB12']",,612254,,,,,,,,,,
mondo:0012837,inflammatory bowel disease 15,"['inflammatory bowel disease 15', 'inflammatory bowel disease type 15', 'IBD15']",0110897,612255,,C2677094,,,,C567381,,,,
mondo:0012838,inflammatory bowel disease 16,"['inflammatory bowel disease type 16', 'inflammatory bowel disease 16', 'IBD16']",0110896,612259,,C2677093,,,,C567380,,,,
mondo:0012839,pyogenic bacterial infections due to MyD88 deficiency,"['recurrent pyogenic bacterial infections due to MyD88 deficiency', 'immunodeficiency 68', 'MYD88D', 'MyD88 deficiency', 'pyogenic bacterial infections, recurrent, due to MyD88 deficiency']",,612260,183713,C2677092,"['0.3823', '-0.1195', '-0.3472', '0.1355', '-0.419', '-0.1372', '0.3916', '0.3281', '0.3972', '-0.7896', '-0.2505', '0.3745', '-0.1979', '0.352', '-0.1393', '0.2795', '-0.2568', '-0.387', '-0.221', '-0.7886', '0.04996', '-0.1924', '0.591', '-0.3542', '-0.0692', '-0.02733', '-0.539', '0.2625', '-0.4995', '-0.1873', '0.02934', '0.5835', '0.1316', '0.124', '0.007282', '0.189', '-0.3247', '-0.4878', '-0.1951', '0.0868', '-0.1836', '0.1586', '0.4785', '-0.571', '-0.3438', '0.02486', '-0.4895', '-0.3445', '-0.2683', '0.4036', '-0.4055', '-0.0878', '0.2705', '0.1373', '-0.1372', '0.4036', '0.2378', '-0.3853', '-0.6055', '0.284', '0.0878', '0.835', '-0.201', '0.2495', '0.5234', '0.1403', '0.3906', '-0.05392', '-0.333', '0.4585', '0.1123', '-0.2769', '-0.2291', '-0.1683', '0.396', '0.1755', '0.4805', '-0.03079', '0.3252', '0.1222', '-0.2329', '0.2115', '0.1108', '0.1455', '0.01808', '0.334', '0.1973', '0.2603', '0.1405', '0.2527', '0.7036', '-0.0439', '-0.3887', '0.3418', '0.872', '0.7925', '0.02194', '-0.71', '-0.2412', '-0.1189']",,,C567379,,,,
mondo:0012840,inflammatory bowel disease 17,"['inflammatory bowel disease 17', 'inflammatory bowel disease caused by mutation in IL23R', 'inflammatory bowel disease type 17', 'IL23R inflammatory bowel disease', 'IBD17', 'inflammatory bowel disease 17, protection against']",0110883,612261,,C2677091,,,,C567378,,,,
mondo:0012841,inflammatory bowel disease 18,"['IBD18', 'inflammatory bowel disease 18', 'inflammatory bowel disease type 18']",0110888,612262,,C2677090,,,,C567377,,,,
mondo:0012842,"melanoma, cutaneous malignant, susceptibility to, 7","['melanoma, cutaneous malignant, 7', 'melanoma, cutaneous malignant, susceptibility to, 7', 'CMM7']",,612263,,,,,,,,,,
mondo:0012843,"epilepsy, childhood absence, susceptibility to, 5","['childhood absence epilepsy caused by mutation in GABRB3', 'epilepsy, childhood absence, susceptibility to, 5', 'ECA5', 'susceptibility to childhood absence epilepsy 5', 'epilepsy, childhood absence, susceptibility to, type 5', 'GABRB3 childhood absence epilepsy']",,612269,,,,,,,,,,
mondo:0012844,primary ciliary dyskinesia 8,"['ciliary dyskinesia, primary, 8, with or without situs inversus', 'primary ciliary dyskinesia type 8', 'primary ciliary dyskinesia 8 with or without situs inversus', 'ciliary dyskinesia, primary, 8', 'CILD8']",0110616,612274,,C2677085,,,,C567373,,,,
mondo:0012845,inflammatory bowel disease 19,"['inflammatory bowel disease (Crohn disease) 19', 'inflammatory bowel disease caused by mutation in IRGM', 'inflammatory bowel disease type 19', 'IRGM inflammatory bowel disease', 'IBD19', 'inflammatory bowel disease 19']",0110890,612278,,C2677079,,,,C567372,,,,
mondo:0012846,"generalized epilepsy with febrile seizures plus, type 6","['Gefs+, type 6', 'generalized epilepsy with febrile seizures plus, type 6', 'GEFSP6']",0111300,612279,,C2677078,,,,C567371,,,,
mondo:0012847,autosomal recessive congenital ichthyosis 6,"['ARCI6', 'ichthyosis, congenital, autosomal recessive, Nipal4-related', 'ichthyosis, congenital, autosomal recessive type 6', 'ichthyosis, congenital, autosomal recessive 6', 'autosomal recessive congenital ichthyosis type 6']",0060715,612281,,C2677065,,,,,,,,
mondo:0012848,"Meckel syndrome, type 6","['Meckel-Gruber syndrome, type 6', 'Meckel syndrome 6', 'CC2D2A Meckel syndrome', 'MKS6', 'Meckel syndrome, type 6', 'Meckel syndrome caused by mutation in CC2D2A']",0070120,612284,,C2676790,,,,C567365,,,,
mondo:0012849,Joubert syndrome 9,"['Joubert syndrome type 9', 'CC2D2A Joubert syndrome', 'Joubert syndrome 9', 'Joubert syndrome caused by mutation in CC2D2A', 'Joubert syndrome 9/15, digenic', 'JBTS9']",0111004,612285,,C2676788,,C181002,,C567364,,,,
mondo:0012850,hypophosphatemic nephrolithiasis/osteoporosis 1,"['nephrolithiasis/osteoporosis, hypophosphatemic, type 1', 'NPHLOP1', 'hypophosphatemic nephrolithiasis/osteoporosis type 1', 'nephrolithiasis/osteoporosis, hypophosphatemic, 1']",0080077,612286,,C2676786,,,,C567363,,,,
mondo:0012851,hypophosphatemic nephrolithiasis/osteoporosis 2,"['hypophosphatemic nephrolithiasis/osteoporosis type 2', 'nephrolithiasis/osteoporosis, hypophosphatemic, type 2', 'NPHLOP2', 'nephrolithiasis/osteoporosis, hypophosphatemic, 2']",0080078,612287,,C2676782,,,,C567362,,,,
mondo:0012852,inflammatory bowel disease 20,"['inflammatory bowel disease 20', 'IBD20', 'inflammatory bowel disease type 20']",0110898,612288,,C2676781,,,,C567361,,,,
mondo:0012853,Fontaine progeroid syndrome,"['Fontaine progeroid syndrome', 'dental and eye anomalies, patent ductus arteriosus, and normal intelligence', 'progeroid syndrome, Petty type', 'progeroid syndrome Petty type', 'craniofacial dysostosis, hypertrichosis, Hypoplasia of labia majora, dental and eye anomalies, patent ductus arteriosus, and normal intelligence', 'craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of labia majora, dental and eye anomalies', 'progeroid syndrome congenital Petty type', 'dental and eye anomalies-patent ductus arteriosus-normal intelligence syndrome', 'GCM syndrome', 'FPS', 'Petty-Laxova-Wiedemann syndrome', 'cranofacial dysostosis-hypertrichosis-hypoplasia of labia majora syndrome', 'Gorlin-Chaudhry-Moss syndrome', 'GCMS', 'Petty syndrome', 'Gorlin Chaudhry Moss syndrome', 'progeroid syndrome, congenital, Petty type', 'Petty Laxova Wiedemann syndrome', 'craniofacial dysostosis, hypertrichosis, hypoplasia of labia majora', 'craniofacial dysostosis-genital, dental, cardiac anomalies syndrome']",,612289,2963,C2931653,"['-0.11993', '-0.1257', '0.08344', '-0.6436', '0.926', '-0.3955', '-0.3188', '0.932', '-0.2013', '-0.2795', '-0.5527', '-0.2468', '-0.04144', '0.2346', '-0.453', '-0.01643', '0.868', '-0.269', '-0.03217', '-1.01', '0.005142', '-0.3433', '0.1362', '0.05374', '0.2766', '0.5435', '-0.6577', '0.1467', '0.9243', '-0.0943', '0.6445', '0.1131', '-0.05884', '0.08765', '0.13', '-0.363', '-0.4114', '-0.1229', '0.09015', '-0.778', '0.1384', '-0.5776', '-0.42', '-0.2026', '0.295', '-0.845', '0.3071', '0.581', '-0.2915', '-0.1395', '-0.2063', '0.378', '-0.015396', '-0.1749', '-1.0625', '-0.5264', '-0.0013895', '-0.3455', '0.1918', '0.234', '0.01657', '-0.04053', '-0.3757', '-0.1625', '-0.04816', '-0.06335', '-0.12195', '0.5693', '-0.5127', '0.4573', '-0.4268', '0.5884', '0.2722', '-0.03607', '-0.3093', '0.04297', '-0.08875', '-0.512', '-0.492', '-0.4287', '0.2224', '0.5806', '-0.02739', '0.563', '-0.1819', '-0.3484', '-0.05838', '0.2104', '-0.01607', '0.2437', '0.3308', '0.8765', '0.3298', '0.765', '0.6826', '-0.06274', '-0.1614', '0.00972', '0.5767', '0.1661']",,,C537290,759.89,,,
mondo:0012854,bilateral microtia-deafness-cleft palate syndrome,"['microtia with or without hearing impairment', 'microtia with or without hearing impairment (AD)', 'microtia, hearing impairment, and cleft palate (AR)', 'microtia, hearing impairment, and cleft palate']",,612290,140963,C2676772,"['-0.01073', '0.2074', '-0.0199', '-0.09155', '0.2502', '-0.3103', '0.07227', '0.4507', '-0.1891', '-0.4114', '-0.1345', '-0.2527', '-0.07355', '-0.1338', '-0.1083', '-0.0882', '0.12085', '-0.2008', '-0.2537', '-0.1912', '-0.0179', '0.038', '0.2162', '-0.2367', '0.1973', '0.10724', '-0.3428', '-0.04074', '0.365', '-0.2747', '0.1989', '0.02577', '0.1869', '0.03598', '-0.008835', '-0.3645', '-0.06555', '-0.4832', '-0.1982', '-0.2883', '0.1382', '-0.12225', '-0.02016', '-0.386', '-0.1721', '0.023', '0.03073', '0.1514', '-0.2678', '-0.02794', '-0.1403', '-0.215', '0.0863', '-0.2155', '-0.03638', '-0.243', '0.2341', '-0.2383', '-0.278', '0.25', '0.1251', '-0.0388', '-0.009254', '0.1378', '-0.3306', '-0.0992', '-0.01478', '0.3762', '-0.4736', '0.1797', '-0.2922', '0.1809', '0.1425', '-0.11395', '0.002993', '-0.037', '0.1146', '-0.09656', '-0.1512', '0.03123', '0.1277', '0.1708', '0.01277', '0.5786', '-0.0952', '0.003616', '-0.046', '0.525', '-0.02122', '0.1333', '0.08795', '0.5127', '0.1902', '0.0709', '0.773', '-0.1575', '0.3132', '-0.6567', '0.1613', '0.1638']",,,C567359,,,,
mondo:0012855,Joubert syndrome 8,"['Joubert syndrome 8', 'Joubert syndrome caused by mutation in ARL13B', 'Joubert syndrome type 8', 'ARL13B Joubert syndrome', 'JBTS8']",0111003,612291,,C2676771,,,,C567358,,,,
mondo:0012856,Birk-Barel syndrome,"['mental retardation with hypotonia and Facial Dysmorphism', 'intellectual disability-hypotonia-facial dysmorphism syndrome', 'intellectual disability, Birk-Barel type', 'BIRK-Barel mental retardation dysmorphism syndrome', 'Birk Barel mental retardation dysmorphism syndrome', 'Birk-Barel syndrome', 'BIRK-Barel intellectual disability dysmorphism syndrome', 'intellectual disability with hypotonia and Facial Dysmorphism', 'Birk Barel intellectual disability dysmorphism syndrome']",0050675,612292,166108,C2676770,"['-0.2617', '0.1674', '-0.0993', '-0.071', '-0.1449', '-0.7485', '0.05203', '0.4429', '-0.7603', '-0.4568', '0.1586', '-0.1771', '0.1642', '-0.1007', '-0.2505', '0.2966', '0.1512', '-0.2218', '-0.3818', '-0.5327', '0.2878', '0.3274', '-0.06128', '-0.11334', '0.4202', '-0.175', '0.2612', '0.1681', '-0.2876', '0.1001', '0.387', '-0.03497', '0.1738', '0.1404', '-0.0834', '0.0876', '0.1783', '-0.07355', '-0.2917', '-0.4517', '0.4944', '-0.02908', '-0.391', '0.3', '-0.3445', '-0.0767', '-0.189', '0.006947', '0.321', '0.487', '-0.6494', '-0.04068', '-0.4587', '-0.1559', '-0.3396', '-0.7617', '0.03638', '0.4187', '0.4402', '0.536', '0.2264', '-0.02025', '0.1318', '-0.2893', '-0.497', '0.0819', '0.01189', '0.477', '-0.705', '0.206', '-0.2546', '0.2927', '0.1646', '-0.06168', '-0.3218', '0.08936', '0.0882', '0.315', '-0.338', '0.3604', '0.3079', '-0.167', '0.271', '-0.10077', '0.2058', '0.738', '-0.3372', '0.1289', '0.279', '0.9517', '-0.309', '0.04694', '-0.747', '0.2727', '0.8687', '0.00825', '0.3694', '-0.4004', '0.491', '0.3455']",,,C567357,,,,
mondo:0012857,"porokeratosis 5, disseminated superficial actinic type","['porokeratosis, disseminated superficial actinic, 3', 'POROK5', 'porokeratosis 5, disseminated superficial actinic type', 'porokeratosis 5, disseminated superficial actinic']",,612293,,C2676769,,,,C567356,,,,
mondo:0012858,primary CD59 deficiency,"['hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy', 'HACD59', 'CD59 deficiency']",,612300,169464,C2676767,"['-0.3877', '0.007668', '-0.05814', '-0.108', '0.2156', '-0.03653', '-0.2554', '-0.1128', '-0.2908', '0.3438', '-0.1714', '0.2396', '0.223', '0.021', '-0.02182', '-0.34', '0.04172', '0.04742', '-0.10913', '-0.5913', '0.3315', '-0.3318', '0.3767', '-0.07434', '0.1609', '0.2715', '0.0334', '-0.16', '-0.06445', '-0.06058', '0.236', '0.3057', '0.4019', '-0.07086', '0.1929', '-0.3257', '-0.1893', '-0.0974', '-0.1301', '-0.5244', '-0.2174', '0.0565', '0.0905', '-0.1045', '-0.1736', '-0.1521', '-0.11774', '-0.1841', '-0.02538', '0.3179', '0.02069', '0.1095', '0.149', '-0.2327', '-0.1925', '-0.02325', '0.426', '-0.5464', '-0.3271', '0.04922', '0.05872', '0.3057', '0.07306', '0.06464', '0.1821', '0.301', '0.2747', '0.4597', '-0.2793', '0.2026', '-0.2247', '-0.1567', '-0.08813', '-0.11346', '-0.01247', '-0.378', '0.2578', '0.2666', '0.1708', '-0.07605', '-0.1572', '-0.3484', '0.1798', '0.325', '-0.1475', '-0.286', '0.249', '0.1897', '0.243', '-0.0887', '0.4177', '-0.07104', '0.11505', '-0.0481', '0.6133', '0.3835', '0.3652', '-0.02884', '-0.3604', '0.02014']",,,C567355,,,,
mondo:0012859,autosomal recessive osteopetrosis 7,"['TNFRSF11A osteopetrosis (disease)', 'osteopetrosis-hypogammaglobulinemia syndrome', 'osteopetrosis, osteoclast-poor, with hypogammaglobulinemia', 'autosomal recessive osteopetrosis type 7', 'osteoclast-poor osteopetrosis with hypogammaglobulinemia', 'osteopetrosis, autosomal recessive type 7', 'osteopetrosis autosomal recessive 7', 'osteopetrosis osteoclast-poor with hypogammaglobulinemia', 'OPTB7', 'osteopetrosis, autosomal recessive 7', 'autosomal recessive osteoclast-poor osteopetrosis with hypogammaglobulinemia']",0110946,612301,178389,C2676766,"['-0.3843', '0.2397', '0.6553', '-0.8203', '0.4077', '-0.2874', '-0.01793', '0.5347', '-0.04263', '-0.281', '0.0671', '0.0685', '-0.438', '-0.3079', '0.1084', '-0.02911', '0.1925', '-0.1344', '-0.2715', '-0.679', '0.03348', '-0.4648', '0.3784', '-0.2727', '0.2007', '0.08374', '0.2023', '-0.2072', '-0.3945', '-0.32', '-0.003345', '0.1956', '0.2783', '0.1247', '0.00596', '-0.1436', '-0.1586', '-0.4375', '-0.3462', '-0.554', '-0.1638', '0.1244', '0.3918', '-0.1846', '-0.626', '-0.622', '-0.2795', '-0.1554', '0.3508', '-0.0462', '0.2727', '-0.002876', '0.408', '-0.05478', '0.1459', '-0.547', '0.1658', '0.2463', '-0.2842', '0.06006', '0.1377', '0.1176', '0.02565', '-0.3115', '-0.01869', '-0.0592', '0.508', '0.57', '-0.1311', '0.2192', '-0.282', '-0.2185', '-0.2727', '0.1768', '0.2598', '-0.3347', '0.19', '0.3882', '0.2764', '0.06445', '-0.2954', '-0.253', '0.4353', '0.206', '-0.484', '-0.1737', '0.536', '0.2302', '0.2576', '0.1782', '0.0976', '0.01073', '-0.4744', '-0.3047', '0.6865', '1.0205', '0.3152', '-0.3865', '0.00546', '-0.1837']",,,C567354,,,,
mondo:0012860,"thrombophilia due to protein C deficiency, autosomal recessive","['hereditary thrombophilia due to congenital protein C deficiency', 'Proc deficiency, autosomal recessive', 'autosomal recessive protein C deficiency', 'thrombophilia 3 due to protein C deficiency, autosomal recessive', 'thrombophilia due to PROTEIN C deficiency, autosomal recessive', 'thrombophilia due to protein C deficiency, autosomal recessive', 'hereditary thrombophilia due to PC deficiency', 'THPH4', 'autosomal recessive hereditary thrombophilia due to protein C deficiency', 'Protein C deficiency, autosomal recessive']",0111904,612304,,C2676759,,,,C567353,,,,
mondo:0012861,premature ovarian failure 6,"['FIGLA primary ovarian failure', 'premature ovarian failure 6', 'Pof6', 'primary ovarian failure caused by mutation in FIGLA', 'premature ovarian failure type 6']",0080863,612310,,C2676742,,,,C567351,,,,
mondo:0012862,"attention deficit-hyperactivity disorder, susceptibility to, 5","['attention Deficit-hyperactivity disorder, susceptibility to, type 5', 'ADHD5', 'attention deficit-hyperactivity disorder, susceptibility to, 5', 'motor timing quantitative trait locus']",,612311,,,,,,,,,,
mondo:0012863,"attention deficit-hyperactivity disorder, susceptibility to, 6","['ADHD6', 'attention Deficit-hyperactivity disorder, susceptibility to, type 6', 'attention deficit-hyperactivity disorder, susceptibility to, 6', 'digit span quantitative trait locus']",,612312,,,,,,,,,,
mondo:0012864,chromosome 2q32-q33 deletion syndrome,"['monosomy 2q32-q33', 'glass', '2q32q33 microdeletion syndrome', 'monosomy 2q32q33', 'glass syndrome', 'monosomy 2q32', 'SAS', 'Del(2)(q32)', 'Del(2)(q32q33)', 'SATB2-associated syndrome', 'SATB2 syndrome', '2q32-q33 microdeletion syndrome', '2q32q33 microdeletion syndromes', 'chromosome 2q32-q33 deletion syndrome']",0060428,612313,576283,C4304531,,,,C567350,,,,
mondo:0012865,Pseudofolliculitis barbae,"['PFB', 'ingrown hairs', 'pili Incarnati', 'pseudofolliculitis barbae, susceptibility to', 'Pseudofolliculitis barbae']",,612318,,C0549150,,,,C563016,,L73.1,,
mondo:0012866,hereditary spastic paraplegia 35,"['leukodystrophy, dysmyelinating and spastic paraparesis with or without dystonia', 'autosomal recessive spastic paraplegia type 35', 'hereditary spastic paraplegia caused by mutation in FA2H', 'autosomal recessive spastic paraplegia 35', 'FA2H hereditary spastic paraplegia', 'hereditary spastic paraplegia type 35', 'leukodystrophy, dysmyelinating, and spastic paraparesis with or without dystonia', 'spastic paraplegia 35, autosomal recessive', 'SPG35']",0110786,612319,171629,C3496228,"['-0.0858', '0.3384', '-0.02196', '-0.5737', '-0.096', '-0.605', '-0.5483', '0.1868', '-0.543', '0.2054', '-0.5767', '-0.0695', '-0.1108', '-0.414', '0.4973', '-0.3625', '0.04956', '-0.5127', '-0.2742', '-0.2961', '-0.10406', '-0.375', '0.0756', '0.2898', '0.11273', '0.07227', '-0.2844', '-0.1578', '-0.4233', '-0.305', '0.04108', '0.006195', '0.54', '0.02295', '0.1412', '0.0674', '-0.4614', '-0.311', '-0.015335', '-0.2289', '0.589', '-0.854', '0.1376', '0.404', '0.04932', '-0.4883', '-0.2098', '0.05508', '-0.2952', '-0.3616', '0.3003', '0.6846', '-0.5635', '0.01403', '-0.1903', '-0.11505', '0.4263', '-0.1392', '-0.313', '0.2522', '-0.1232', '-0.1063', '0.334', '-0.153', '-0.822', '0.3276', '0.6465', '0.569', '-0.3503', '0.545', '-0.2267', '0.3196', '0.0921', '-0.234', '0.591', '0.05298', '-0.0784', '-0.0545', '-0.0495', '-0.3293', '-0.2301', '-0.326', '0.5327', '0.929', '0.288', '0.1416', '-0.03564', '0.4495', '0.503', '-0.169', '0.572', '0.4873', '0.2303', '0.246', '0.815', '0.5605', '0.4229', '0.3652', '0.05566', '0.0585']",,,C567311,,,,
mondo:0012867,hereditary spastic paraplegia 38,"['autosomal dominant spastic paraplegia type 38', 'SPG38', 'hereditary spastic paraplegia type 38', 'autosomal dominant spastic paraplegia 38', 'spastic paraplegia 38, autosomal dominant']",0110789,612335,171617,C2676732,,,,C567349,,,,
mondo:0012868,"thrombophilia due to protein S deficiency, autosomal dominant","['hereditary thrombophilia due to congenital protein S deficiency, autosomal dominant', 'autosomal dominant hereditary thrombophilia due to congenital protein S deficiency', 'thrombophilia 5 due to protein S deficiency, autosomal dominant', 'protein S acquired deficiency', 'thrombophilia due to protein S deficiency, autosomal dominant', 'THPH5']",0111900,612336,26349,C3278211,,,,C567077,,,10068370,
mondo:0012869,"intellectual disability, autosomal dominant 22","['autosomal dominant non-syndromic intellectual disability 22', 'autosomal dominant mental retardation 22', 'chromosome 1Qter deletion syndrome', 'autosomal dominant non-syndromic intellectual disability caused by mutation in ZBTB18', 'intellectual disability, autosomal dominant 22', 'MRD22', 'autosomal dominant intellectual disability 22', 'intellectual disability, autosomal dominant type 22', 'ZBTB18 autosomal dominant non-syndromic intellectual disability', 'mental retardation, autosomal dominant 22', 'mental retardation, autosomal dominant type 22', 'chromosome 1Q43-q44 deletion syndrome']",0070052,612337,36367,C3808184,"['-0.533', '0.05124', '0.588', '-0.4204', '0.2422', '-0.11615', '0.2458', '0.485', '-0.4119', '-0.2441', '-0.2169', '-0.2522', '0.2335', '-0.12177', '-0.2231', '-0.07294', '0.01884', '-0.01552', '-0.539', '-0.5117', '0.3127', '0.2411', '0.2244', '0.01551', '0.174', '-0.2302', '0.02495', '-0.1611', '0.11615', '-0.1873', '0.3406', '-0.2045', '0.537', '0.287', '0.004673', '0.1908', '-0.2197', '0.01361', '-0.2454', '-0.144', '0.143', '-0.2013', '0.11456', '0.05615', '0.163', '-0.6616', '0.344', '0.0898', '-0.3281', '-0.1495', '-0.3337', '0.0316', '-0.1034', '-0.02321', '-0.2029', '-0.1786', '0.1316', '-0.0686', '-0.3748', '0.254', '-0.0176', '-0.1821', '0.01291', '0.2786', '-0.058', '0.04807', '0.3083', '0.242', '-0.542', '0.3125', '-0.2253', '0.02548', '-0.01726', '-0.007008', '-0.3206', '-0.2001', '0.427', '-0.2766', '-0.36', '0.0573', '0.1665', '0.267', '-0.0468', '0.494', '0.0882', '-0.1202', '0.2023', '0.3694', '0.2183', '0.06384', '0.1519', '0.6777', '0.1371', '0.1526', '0.71', '-0.02696', '0.6074', '-0.1998', '0.3086', '0.4258']",,,C567346,,,,
mondo:0012870,chromosome 2q31.2 deletion syndrome,['chromosome 2q31.2 deletion syndrome'],0060416,612345,,C2676724,,,,C567344,,,,
mondo:0012871,Jervell and Lange-Nielsen syndrome 2,"['Jervell and Lange-Nielsen syndrome caused by mutation in KCNE1', 'KCNE1 Jervell and Lange-Nielsen syndrome', 'Jervell and Lange-Nielsen syndrome type 2', 'JLNS2', 'Jervell and Lange-Nielsen syndrome 2']",,612347,,,,,,C567343,,,,
mondo:0012872,"thrombophilia, familial, due to decreased release of tissue plasminogen activator","['hyperfibrinolysis, familial, due to increased release of tissue plasminogen activator', 'thrombophilia, familial, due to decreased release of tissue plasminogen activator', 'thrombophilia, familial, due to decreased release of PLAT', 'THPH9', 'hyperfibrinolysis, familial, due to increased release of plat']",0111906,612348,,,,,,C567341,,,,
mondo:0012873,"Ehlers-Danlos syndrome, spondylocheirodysplastic type","['EDS, spondylocheirodysplastic type', 'SCD-EDS', 'spondylocheirodysplasia, Ehlers-Danlos syndrome-like', 'EDSSPD3', 'Ehlers-Danlos syndrome, spondylodysplastic type, 3']",0080739,612350,157965,C2676510,"['-0.1802', '-0.10535', '-0.0966', '-0.1628', '0.11035', '-0.4543', '-0.251', '1.079', '-0.6206', '0.4587', '-0.06146', '-0.3162', '0.121', '0.762', '-0.2773', '0.291', '-0.3003', '0.3354', '-0.2035', '-0.4722', '0.2717', '0.731', '0.6313', '0.2637', '-0.3162', '0.2365', '-0.2407', '0.4263', '1.039', '0.1655', '1.169', '-0.716', '0.06354', '-0.07275', '0.1711', '0.1896', '-0.1829', '-0.218', '0.2542', '-0.8394', '0.8374', '-0.4517', '-0.8696', '0.1586', '0.04996', '-0.2198', '-0.2954', '0.8184', '0.3018', '-0.9077', '0.1744', '-0.624', '0.5044', '0.05032', '-0.02852', '-0.6934', '-0.659', '-0.01341', '0.4663', '-0.12006', '-0.2152', '0.1991', '-0.1934', '-0.1251', '0.010925', '0.4106', '-0.7607', '0.901', '0.2524', '0.518', '-0.6753', '0.1423', '-0.4812', '-0.1226', '0.04788', '0.05844', '-0.1035', '-0.4333', '0.2352', '0.01903', '-0.04166', '-0.01263', '0.1948', '0.5747', '-0.836', '0.1686', '-0.3628', '0.6333', '0.1698', '-0.2761', '0.4639', '0.3755', '-0.687', '0.2335', '0.675', '0.226', '0.806', '-0.375', '-0.003855', '0.1008']",,,C567340,,,,
mondo:0012874,"porokeratosis 6, disseminated superficial actinic type","['porokeratosis, disseminated superficial actinic, 4', 'porokeratosis 6, disseminated superficial actinic type', 'porokeratosis 6, disseminated superficial', 'POROK6', 'porokeratosis 6, multiple types']",,612353,,C2676508,,,,C567339,,,,
mondo:0012875,inflammatory bowel disease 21,"['IBD21', 'inflammatory bowel disease type 21', 'inflammatory bowel disease 21']",0110906,612354,,C2676507,,,,C567338,,,,
mondo:0012876,heparin cofactor 2 deficiency,"['Hcf2 deficiency', 'heparin cofactor II deficiency', 'thrombophilia 10 due to heparin cofactor II deficiency', 'thrombophilia due to heparin cofactor 2 deficiency', 'Hcf 2 deficiency']",0111901,612356,,C0398626,,,,C562865,286.3,,,
mondo:0012877,major affective disorder 8,"['MAFD8', 'bipolar affective disorder', 'major affective disorder 8', 'MAJOR affective disorder 8', 'major affective disorder-8, susceptibility to']",,612357,,,,,,C567530,,,,
mondo:0012878,Cowden syndrome 2,"['Cowden syndrome 2', 'CWS2', 'SDHB Cowden disease', 'Cowden syndrome type 2', 'Cowden disease caused by mutation in SDHB']",,612359,,C3552552,,,,C567337,,,,
mondo:0012879,schizophrenia 14,"['schizophrenia type 14', 'schizophrenia 14', 'SCZD14', 'schizophrenia, susceptibility to, 14', 'schizophrenia susceptibility locus, chromosome 2Q32-related', 'Sczd14']",0070090,612361,,C2677614,,,,,,,,
mondo:0012880,hypogonadotropic hypogonadism 5 with or without anosmia,"['Kallmann syndrome 5', 'KAL5', 'hypogonadotropic hypogonadism caused by mutation in CHD7', 'hypogonadotropic hypogonadism 5 with or without anosmia', 'HH5', 'CHD7 hypogonadotropic hypogonadism']",0090084,612370,,C3552553,,,,C567220,,E23.0,,
mondo:0012881,major affective disorder 7,"['major affective disorder type 7', 'bipolar affective disorder', 'major affective disorder 7', 'major affective disorder-7, susceptibility to', 'MAFD7']",,612371,,,,,,C567529,,,,
mondo:0012882,major affective disorder 9,"['bipolar affective disorder', 'major affective disorder-9, susceptibility to', 'MAJOR affective disorder 9', 'major affective disorder 9', 'MAFD9']",,612372,,,,,,C567531,,,,
mondo:0012883,acute promyelocytic leukemia,"['FAB M3', 'acute myeloid leukaemia with t(15;17)(q22;q12);(PML/RARalpha) and variants', 'acute promyelocytic leukemia with PML-rara', 'AML M3', 'promyelocytic leukaemia', 'APL', 'leukemia, acute promyelocytic, somatic', 'APML', 'AML with t(15;17)(q22;q12);(PML/RARalpha) and variants', 'promyelocytic leukemia', 'acute promyelocytic leukemia', 'acute promyelocytic leukemia with t(15;17)(q22;q12); PML/rara', 'acute myeloblastic leukemia type 3', 'AML with t(15;17)(q22;q12)', 'leukemia, acute promyelocytic', 'acute myeloblastic leukaemia 3', 'acute myeloid leukemia M3', 'acute promyelocytic leukaemia with t(15;17)(q22;q12); PML-rara', 'acute myeloid leukemia with t(15;17)(q22;q12);(PML/RARalpha) and variants', 'acute myeloblastic leukaemia type 3', 'acute myeloblastic leukemia 3', 'acute myeloid leukaemia M3', 'APML - acute promyelocytic leukemia', 'acute promyelocytic leukaemia with t(15;17)(q22;q12); PML/rara', 'APML - acute promyelocytic leukaemia', 'acute promyelocytic leukaemia with PML-rara', 'acute promyelocytic leukemia with t(15;17)(q22;q12); PML-rara']",0081081,612376,520,C0023487,"['0.229', '-0.3936', '-0.1592', '0.01543', '-0.4253', '-0.492', '0.597', '1.402', '-0.007614', '-0.351', '0.1652', '0.3313', '0.0848', '0.2622', '-0.1663', '0.2094', '-0.0665', '-0.506', '-0.08716', '-0.1846', '-0.318', '-0.413', '0.737', '-0.908', '0.276', '-0.386', '0.0435', '-0.694', '-0.5674', '0.3276', '0.8086', '0.8735', '1.05', '-0.07385', '0.2067', '0.1667', '-1.361', '0.4956', '0.2212', '-0.4346', '0.332', '0.2202', '0.016', '-0.746', '-0.2588', '-0.1761', '-0.3958', '-0.2253', '0.2896', '-0.421', '0.5986', '-0.3018', '0.3577', '-0.3496', '0.9023', '0.3008', '-0.7427', '-0.0628', '-0.7886', '-0.0925', '0.03049', '0.2252', '0.2413', '-0.7905', '-0.354', '0.05307', '0.0576', '-0.2595', '0.0799', '1.295', '-0.1793', '-0.2032', '-0.2998', '-0.2744', '0.692', '0.0857', '0.456', '0.638', '0.0799', '-0.313', '-0.816', '-0.504', '0.07806', '-0.1404', '-0.289', '-0.584', '0.796', '0.599', '0.4177', '0.008934', '0.1351', '-0.00515', '-0.6714', '0.2224', '0.7573', '0.9897', '-0.0952', '-0.5483', '-0.3455', '-0.02689']",C3182,0000224,D015473,,,10001019,
mondo:0012884,"systemic lupus erythematosus, susceptibility to, 13","['systemic lupus erythematosus, susceptibility to, 13', 'SLEB13']",,612378,,,,,,,,,,
mondo:0012885,SRD5A3-congenital disorder of glycosylation,"['SRD5A3-CDG (CDG-Iq)', 'congenital disorder of glycosylation type 1q', 'congenital disorder of glycosylation type Iq', 'SRD5A3-CDG', 'CDGIq', 'congenital disorder of glycosylation, type Iq', 'coloboma, ocular, with ichthyosis, brain malformations, and endocrine abnormalities', 'CDG1Q', 'CDG syndrome type Iq', 'CDG-Iq', 'congenital disorder of glycosylation due to steroid 5alpha-reductase type 3 deficiency', 'CDG Iq']",0080568,612379,324737,C4317224,"['-0.5815', '-0.259', '0.006523', '-0.0915', '0.611', '-0.4001', '0.231', '0.1814', '-0.761', '-0.2495', '-0.4', '0.1382', '0.02403', '-0.18', '-0.3066', '-0.4072', '0.3555', '-0.2336', '0.0823', '-0.6636', '0.1903', '-0.05054', '0.3396', '-0.0724', '0.0734', '-0.12024', '-0.3933', '0.11206', '0.3499', '-0.1849', '0.645', '0.545', '0.6006', '0.629', '-0.434', '-0.937', '-0.1616', '-0.4878', '-0.51', '-0.2208', '0.1294', '-0.364', '0.00478', '0.5117', '0.005867', '-0.3152', '0.3186', '0.4626', '-0.1238', '0.0699', '0.0173', '0.519', '0.2432', '-0.3516', '-0.05612', '0.11786', '1.122', '0.3674', '-0.436', '0.0621', '-0.3418', '0.361', '-0.02812', '0.468', '-0.2664', '-0.1761', '0.4246', '0.608', '0.2598', '-0.1517', '-0.5615', '0.1384', '-0.10736', '-0.2397', '0.1947', '-0.12494', '0.7085', '-0.559', '-0.1226', '-0.0799', '-0.2925', '-0.12177', '0.05164', '0.512', '-0.214', '-0.2725', '0.421', '0.986', '0.2225', '0.6387', '0.1982', '0.626', '0.581', '-0.4753', '1.102', '0.1292', '0.519', '0.574', '0.3582', '0.278']",,,,,,,
mondo:0012886,inflammatory bowel disease 22,"['inflammatory bowel disease type 22', 'IBD22', 'inflammatory bowel disease 22']",0110905,612380,,C2676485,,,,C567327,,,,
mondo:0012887,inflammatory bowel disease 23,"['IBD23', 'inflammatory bowel disease type 23', 'inflammatory bowel disease 23']",0110884,612381,,C2676484,,,,C567326,,,,
mondo:0012888,"sarcoidosis, susceptibility to, 2","['BTNL2 sarcoidosis', 'SS2', 'susceptibility to sarcoidosis 2', 'sarcoidosis, susceptibility to, type 2', 'sarcoidosis, susceptibility to, 2', 'sarcoidosis caused by mutation in BTNL2']",,612387,,,,,,,,,,
mondo:0012889,"sarcoidosis, susceptibility to, 3","['SS3', 'sarcoidosis, susceptibility to, 3']",,612388,,,,,,,,,,
mondo:0012890,pontocerebellar hypoplasia type 2B,"['PCH2B', 'pontocerebellar hypoplasia, type 2B', 'non-syndromic pontocerebellar hypoplasia caused by mutation in TSEN2', 'TSEN2 non-syndromic pontocerebellar hypoplasia']",0060268,612389,,C2676466,,,,C567325,,,,
mondo:0012891,pontocerebellar hypoplasia type 2C,"['TSEN34 non-syndromic pontocerebellar hypoplasia', 'PCH2C', 'pontocerebellar hypoplasia, type 2C', 'non-syndromic pontocerebellar hypoplasia caused by mutation in TSEN34']",0060269,612390,,C2676465,,,,C567324,,,,
mondo:0012892,"bone fragility with contractures, arterial rupture, and deafness","['lysyl Hydroxylase 3 deficiency', 'bone fragility with contractures, arterial rupture, and deafness', 'LH3 deficiency', 'bone fragility-contractures-arterial rupture-deafness syndrome', 'connective tissue disorder due to LH3 deficiency', 'connective tissue disorder due to lysyl hydroxylase-3 deficiency']",,612394,300284,C2676285,"['-0.553', '-0.2063', '0.1925', '-0.3237', '0.4124', '-0.4395', '-0.3032', '0.5405', '-0.5454', '0.0834', '-0.175', '-0.3186', '-0.2129', '-0.456', '-0.6167', '0.3164', '0.5664', '-0.0977', '-0.82', '-0.542', '0.6406', '-0.274', '0.458', '-0.1942', '0.06647', '0.2433', '0.085', '0.00963', '0.354', '-0.1183', '0.4353', '-0.1209', '0.482', '0.8027', '0.2478', '-0.173', '0.0718', '0.282', '-0.1357', '-0.5083', '0.4006', '-0.1362', '-0.276', '0.4014', '-0.06287', '-0.3325', '0.347', '0.4302', '0.1277', '0.001124', '-0.521', '-0.4', '0.7065', '0.5854', '-0.4155', '-0.3564', '0.4758', '-0.3074', '0.00905', '-0.0364', '0.0128', '-0.1737', '-0.821', '-0.1489', '0.251', '0.12256', '0.176', '0.52', '-0.506', '0.413', '-0.8115', '0.1381', '-0.0641', '0.2551', '-0.3884', '-0.2573', '0.4224', '0.365', '-0.2566', '0.014084', '-0.0361', '-0.4136', '0.11066', '0.317', '-0.0592', '-0.3977', '-0.3115', '0.4814', '0.2013', '0.03662', '0.6025', '0.6504', '0.2734', '-0.0972', '0.5522', '0.5513', '0.4087', '0.1571', '0.4172', '0.2566']",,,C567320,,,,
mondo:0012893,osteoarthritis susceptibility 5,"['osteoarthritis caused by mutation in GDF5', 'osteoarthritis susceptibility 5', 'osteoarthritis of hip', 'osteoarthritis-5', 'osteoarthritis susceptibility type 5', 'GDF5 osteoarthritis', 'OS5']",,612400,,C0029410,,,,,,,,
mondo:0012894,osteoarthritis susceptibility 6,"['osteoarthritis susceptibility 6', 'OS6', 'osteoarthritis of knee']",,612401,,C0409959,,,,,715.96,,,
mondo:0012895,torsion dystonia 17,"['primary dystonia, DYT17 type', 'dystonia 17, torsion, autosomal recessive', 'torsion dystonia type 17', 'DYT17', 'dystonia-17, primary torsion']",0090042,612406,370103,C2676281,,,,C567319,,,,
mondo:0012896,"psoriasis 10, susceptibility to","['psoriasis susceptibility 10', 'PSORS10', 'psoriasis 10, susceptibility to']",0111289,612410,,,,,,,,,,
mondo:0012897,congenital factor XI deficiency,"['Rosenthal^s disease', 'factor XI deficiency, autosomal dominant', 'hereditary factor XI deficiency', 'Rosenthal factor deficiency', 'factor 11 deficiency', 'PTA deficiency', 'congenital factor XI deficiency', 'hereditary Factor XI deficiency', 'factor XI deficiency, autosomal recessive', 'plasma thromboplastin antecedent deficiency', 'hereditary factor XI deficiency disease', 'factor XI deficiency', 'haemophilia C', 'hemophilia C', 'Rosenthal syndrome', 'F11 deficiency']",2229,612416,329,C0015523,"['-0.1736', '-0.1192', '-1.058', '-0.5073', '-0.326', '0.4856', '-0.2487', '0.5684', '0.02422', '0.1267', '-0.1182', '0.513', '0.4011', '0.3374', '-0.435', '-0.1643', '0.05557', '-0.1469', '-0.513', '-0.3706', '-0.3105', '-0.4104', '0.8984', '0.174', '-0.213', '-0.3005', '-0.1617', '-0.2445', '0.1769', '0.2407', '0.2585', '-0.2698', '0.357', '0.5874', '-0.04843', '-0.273', '0.05536', '-0.5474', '0.12146', '0.04028', '0.1796', '-0.3', '0.1009', '-0.2502', '0.3381', '0.2854', '-0.1602', '-0.02992', '0.3438', '0.3303', '0.487', '-0.597', '0.4219', '-0.1512', '-0.701', '0.4705', '0.4148', '-0.1932', '-0.5464', '0.1741', '-0.1215', '-0.0289', '0.5244', '-0.1615', '0.1293', '0.663', '0.5815', '0.1411', '-0.3284', '-0.1517', '-0.1978', '-0.2095', '-0.1895', '-0.3804', '0.4858', '0.1344', '0.8887', '0.01289', '0.02222', '0.06854', '-0.688', '-0.2386', '0.1023', '0.0324', '-0.1117', '0.1733', '0.3813', '0.3274', '0.4634', '-0.36', '0.1493', '0.7544', '0.3079', '0.2734', '0.705', '0.4695', '0.1882', '-0.722', '-0.0833', '-0.0709']",C84705,,,286.2,,,
mondo:0012898,"narcolepsy 4, susceptibility to","['narcolepsy 4', 'narcolepsy 4, susceptibility to', 'NRCLP4']",,612417,,C2676275,,,,,,,,
mondo:0012899,"alopecia, androgenetic, 3","['AGA3', 'alopecia, androgenetic, 3']",,612421,,C2676272,,,,C567317,,,,
mondo:0012900,"cardiomyopathy, familial restrictive, 3","['cardiomyopathy, familial restrictive, type 3', 'cardiomyopathy, familial restrictive, 3', 'RCM3', 'TNNT2 familial isolated restrictive cardiomyopathy', 'familial isolated restrictive cardiomyopathy caused by mutation in TNNT2']",0111427,612422,,C2676271,,,,C567316,,,,
mondo:0012901,inherited prekallikrein deficiency,"['PKK deficiency', 'hereditary prekallikrein deficiency', 'fletcher factor (prekallikrein) deficiency', 'congenital prekallikrein deficiency', 'prekallikrein deficiency, congenital', 'Fletcher Factor deficiency', 'prekallikrein deficiency']",,612423,749,,"['-0.2183', '-0.277', '-0.3093', '0.0956', '-0.1061', '-0.0499', '0.2482', '-0.3096', '0.3967', '-0.2734', '0.4849', '-0.08435', '0.245', '-0.3787', '-0.1487', '-0.3386', '-0.163', '0.1354', '-0.00792', '-0.892', '0.11456', '0.01671', '0.651', '-0.1412', '0.2006', '-0.2113', '0.138', '-0.01416', '0.2433', '0.0841', '0.4783', '-0.1976', '0.347', '0.1984', '-0.315', '-0.0755', '0.07513', '-0.12354', '0.1088', '-0.2913', '0.1423', '0.06274', '0.3245', '-0.10315', '-0.00412', '0.02647', '-0.1793', '-0.08246', '0.3552', '0.1516', '0.2234', '0.2341', '0.01639', '0.1547', '-0.4062', '-0.1594', '0.1677', '-0.214', '-0.7236', '0.2878', '-0.06134', '0.3591', '0.3477', '-0.266', '0.2253', '0.0826', '-0.0344', '0.3066', '-0.3057', '0.5786', '-0.402', '-0.0514', '0.0803', '0.1469', '0.241', '0.1061', '0.3433', '0.08276', '-0.2375', '-0.1027', '-0.641', '0.1926', '0.1663', '0.10504', '0.1992', '-0.05035', '0.3137', '0.006508', '0.4702', '-0.3237', '0.2422', '0.4065', '0.11676', '-0.1788', '0.527', '0.4448', '0.337', '-0.4526', '-0.388', '0.1915']",,,C562725,286.9,,,
mondo:0012902,autosomal dominant nonsyndromic hearing loss 27,"['autosomal dominant deafness 27', 'DFNA27', 'autosomal dominant nonsyndromic deafness type 27', 'deafness, autosomal dominant 27', 'autosomal dominant nonsyndromic deafness 27']",0110556,612431,,,,,,,,,,
mondo:0012903,autosomal recessive nonsyndromic hearing loss 45,"['deafness, autosomal recessive 45', 'DFNB45', 'autosomal recessive nonsyndromic deafness 45', 'autosomal recessive nonsyndromic deafness type 45', 'autosomal recessive deafness 45']",0110502,612433,,,,,,,,,,
mondo:0012904,"epilepsy, progressive myoclonic, 1B","['epilepsy, progressive myoclonic, 1B', 'epilepsy, progressive myoclonic, type 1B', 'progressive myoclonic epilepsy caused by mutation in PRICKLE1', 'epilepsy, progressive myoclonic 1B', 'EPM1B', 'PRICKLE1 progressive myoclonic epilepsy']",0111448,612437,,C2676254,,,,C580388,345.10,,,
mondo:0012905,hypomyelinating leukodystrophy 6,"['HLD6', 'leukodystrophy, hypomyelinating, with atrophy of the basal ganglia and cerebellum', 'hypomyelinating leukodystrophy with atrophy of the basal ganglia and cerebellum', 'leukodystrophy, hypomyelinating, type 6', 'HABC', 'leukodystrophy, hypomyelinating, 6', 'hypomyelinating leukodystrophy type 6', 'H-ABC', 'hypomyelination with atrophy of basal ganglia and cerebellum']",0060798,612438,139441,C2676244,"['-0.4727', '0.2898', '-0.01921', '-0.4072', '0.2937', '-0.7046', '-0.2993', '0.5527', '-0.6606', '-0.04047', '-0.4143', '-0.0865', '-0.2922', '-0.3718', '0.7896', '-0.06586', '0.176', '-0.2242', '-0.295', '-0.607', '-0.2344', '-0.312', '-0.0879', '-0.524', '-0.09326', '-0.1333', '-0.2659', '-0.0705', '-0.02806', '-0.344', '-0.1553', '0.2935', '0.5933', '0.0269', '0.1964', '-0.267', '-0.406', '-0.283', '-0.011', '0.3474', '0.3882', '-0.872', '-0.419', '0.2285', '0.08295', '-0.231', '-0.11694', '0.4368', '-0.02687', '-0.3672', '0.2432', '0.517', '-0.4822', '0.01837', '0.371', '0.1412', '0.903', '4.73e-05', '-0.192', '0.2148', '-0.12396', '0.3257', '0.9033', '0.1307', '-0.797', '-0.08563', '-0.04666', '1.009', '-0.44', '0.3923', '-0.2239', '0.3054', '-0.10175', '-0.1171', '0.3657', '0.186', '0.006424', '0.5786', '-0.0843', '-0.2296', '0.07306', '-0.1676', '0.212', '0.4668', '0.276', '-0.3098', '-0.1324', '0.2925', '0.3096', '-0.07825', '0.3542', '0.4402', '-0.01791', '0.05994', '0.4033', '0.069', '0.666', '-0.4617', '0.6265', '-0.0737']",,,C567314,,,,
mondo:0012906,primary ciliary dyskinesia 9,"['primary ciliary dyskinesia type 9', 'ciliary dyskinesia, primary, 9', 'ciliary dyskinesia, primary, 9, with or without situs inversus', 'ciliary dyskinesia, primary, type 9', 'primary ciliary dyskinesia caused by mutation in DNAI2', 'primary ciliary dyskinesia 9 with or without situs inversus', 'DNAI2 primary ciliary dyskinesia', 'CILD9']",0110622,612444,,C2676235,,,,C567310,,,,
mondo:0012907,blindness - scoliosis - arachnodactyly syndrome,"['scoliosis, arachnodactyly, and blindness']",,612445,171844,C2676234,,,,C567309,,,,
mondo:0012908,complement component 6 deficiency,"['C6D', 'complement component 6 deficiency', 'classic complement early component deficiency caused by mutation in C6', 'complement component 6 deficiency, subtotal', 'C6 classic complement early component deficiency', 'C6 deficiency, subtotal', 'C6 deficiency']",0060299,612446,,C2676232,,,,,,,,
mondo:0012909,"skeletal defects, genital hypoplasia, and intellectual disability","['skeletal defects, genital hypoplasia, and intellectual disability', 'skeletal defects, genital hypoplasia, and mental retardation']",,612447,,C2676231,"['-0.02725', '0.02234', '0.01643', '-0.02881', '0.02074', '-0.0445', '0.01035', '0.05673', '-0.04233', '-0.0376', '-0.02275', '-0.006477', '-0.00823', '0.02089', '-0.03165', '-0.02399', '-0.00079', '-0.013626', '-0.04218', '-0.076', '0.00831', '-0.007347', '0.03455', '-0.02159', '0.0165', '-0.02359', '-0.007195', '0.001657', '0.00864', '-0.02805', '0.032', '-0.003565', '0.05237', '0.007492', '0.02083', '-0.02394', '-0.02138', '-0.02371', '-0.01584', '-0.03836', '0.02287', '-0.04205', '0.005215', '-0.00894', '-0.00371', '-0.04794', '0.000991', '0.02089', '-0.006683', '0.007545', '-0.02171', '-0.005142', '0.01418', '0.00946', '-0.01746', '-0.0161', '0.02127', '-0.01987', '-0.04932', '0.003368', '0.00866', '0.002903', '-0.01063', '0.001157', '-0.01377', '0.004925', '0.04013', '0.03775', '-0.04523', '0.033', '-0.03525', '0.0038', '0.01712', '-0.02946', '0.01253', '0.00512', '0.02295', '-0.00728', '-0.0339', '-0.0234', '0.004868', '0.001773', '-0.006866', '0.03928', '-0.003216', '-0.003561', '0.01634', '0.03226', '0.05167', '0.00356', '0.011696', '0.04904', '-0.0007343', '0.02092', '0.07983', '0.01804', '0.03363', '-0.05847', '0.002584', '0.02194']",,,C567306,,,,
mondo:0012910,age-related hearing impairment 1,"['presbycusis 1', 'ARHI1', 'age-related hearing impairment 1']",,612448,,C2676230,,,,C567305,,,,
mondo:0012911,pseudohypoparathyroidism type 1C,"['pseudohypoparathyroidism Ic', 'pseudohypoparathyroidism, type 1C', 'pseudohypoparathyroidism, type IC', 'Php 1C', 'PHP1C']",,612462,79444,C2932716,"['-0.2479', '-0.1436', '-0.158', '-0.1681', '-0.571', '0.729', '0.1351', '0.755', '-0.9614', '-1.266', '-0.2238', '-0.05328', '-0.1807', '1.017', '-0.4617', '0.3606', '-0.0491', '-0.547', '-0.1318', '-0.4497', '0.564', '-0.3733', '0.5923', '-0.0148', '0.273', '0.012596', '-0.206', '-0.5586', '0.3704', '-0.7983', '-0.2537', '0.1865', '-0.4976', '0.10657', '-0.11566', '-0.943', '0.2803', '0.3909', '0.404', '0.1967', '0.563', '-0.2042', '0.784', '-0.453', '0.522', '-0.604', '0.89', '0.3704', '0.1353', '0.3076', '0.1462', '0.4202', '0.8433', '-0.3303', '-0.857', '-0.8286', '-0.2346', '-0.772', '-0.506', '-0.3857', '-0.2996', '-0.119', '0.1715', '-0.2211', '-0.57', '1.115', '0.4128', '0.876', '-0.641', '0.1001', '-0.04462', '-0.01463', '0.4094', '-0.2058', '0.5786', '0.671', '9.39e-05', '0.011345', '-0.07104', '0.5454', '0.582', '0.69', '-0.2756', '-0.826', '-0.2693', '-0.542', '-0.02151', '0.4265', '0.73', '0.0781', '0.1117', '0.591', '-0.2605', '-0.2238', '0.1433', '0.2361', '-0.11414', '-0.668', '0.0957', '0.4883']",,,C548076,,,,
mondo:0012912,pseudopseudohypoparathyroidism,"['Albright hereditary osteodystrophy without multiple hormone resistance', 'Albright Hereditary osteodystrophy with multiple hormone resistance', 'aho-PPHP syndrome', 'Pseudopseudo-hypoparathyroidism', 'pseudopseudohypoparathyroidism', 'Albright hereditary osteodystrophy-PPHP syndrome', 'pseudo-pseudohypoparathyroidism', 'Normocalcemic pseudohypoparathyroidism', 'PPHP', 'Normocalcemic pseudohypoparathyroidism (disorder) [ambiguous]']",4183,612463,79445,C0033835,"['-0.11237', '-0.03004', '-0.3054', '-0.08105', '-0.6226', '0.688', '0.138', '0.7676', '-1.127', '-1.089', '-0.2362', '0.0566', '-0.49', '0.94', '-0.4382', '0.3484', '0.11694', '-0.601', '-0.635', '-0.6733', '0.3176', '-0.1522', '0.545', '-0.2957', '0.2852', '0.0246', '-0.1509', '-0.3042', '0.2795', '-0.7373', '-0.3154', '0.0817', '-0.3088', '0.2456', '-0.1716', '-0.6284', '0.1506', '0.138', '0.573', '0.4653', '0.4958', '0.0183', '0.4304', '-0.526', '0.779', '-0.4385', '0.7104', '0.4429', '-0.003761', '0.4849', '0.1383', '0.5825', '0.6646', '0.1389', '-0.74', '-0.7104', '-0.36', '-0.6733', '-0.5977', '-0.5522', '-0.0744', '-0.4067', '0.2546', '-0.3303', '-0.4434', '0.849', '0.4973', '1.125', '-0.545', '0.1439', '0.2152', '-0.04953', '0.496', '-0.306', '0.4944', '0.5225', '0.1918', '0.12415', '0.005108', '0.3938', '0.4065', '0.4226', '-0.2202', '-0.847', '-0.241', '-0.2778', '-0.2993', '0.1653', '0.687', '0.1351', '0.1755', '0.591', '-0.5977', '-0.2695', '0.218', '-0.0345', '0.03564', '-0.823', '0.06866', '0.3665']",C129722,,D011556,275.49,,,
mondo:0012913,"Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome","['chromosome 11P13-p12 deletion syndrome', 'Wilms tumor, aniridia, genitourinary anomalies, mental retardation, and obesity syndrome', 'WAGRO', 'Wilms tumor, aniridia, genitourinary anomalies, intellectual disability, and obesity syndrome', 'Wilms tumor-aniridia-genitourinary anomalies-intellectual disability-obesity syndrome', 'Wagro syndrome', 'Wilms tumor-aniridia-genitourinary anomalies-mental retardation-obesity syndrome', 'WAGR syndrome with obesity']",,612469,,C2675904,,C122804,,C567292,,,,
mondo:0012914,chromosome 1q21.1 deletion syndrome,"['chromosome 1q21.1 deletion syndrome, 1.35-MB', 'Del(1)(q21)', '1q21.1 recurrent microdeletion (susceptibility locus for neurodevelopmental disorders)', 'monosomy 1q21.1', '1q21.1 microdeletion syndrome', 'chromosome 1q21.1 microdeletion syndrome', 'chromosome 1q21.1 deletion syndrome, isolated cases', '1q21.1 microdeletion']",0060411,612474,250989,,,,,,758.33,,,
mondo:0012915,chromosome 1q21.1 duplication syndrome,"['trisomy 1q21.1', '1q21.1 recurrent microduplication (possible susceptibility locus for neurodevelopmental disorders)', 'dup(1)(q21.1)', 'chromosome 1q21.1 duplication syndrome', 'chromosome 1q21.1 duplication syndrome, isolated cases', '1q21.1 microduplication syndrome']",0060435,612475,250994,C2675891,,,,C567290,,,,
mondo:0012916,chromosome 2p16.1-p15 deletion syndrome,"['2p15p16.1 microdeletion syndrome', 'monosomy 2p15-p16.1', '2p15-p16.1 microdeletion syndrome', 'monosomy 2p15p16.1', 'chromosome 2p16.1-p15 deletion syndrome', 'Del(2)(p15p16.1)', 'chromosome 2p16.1-p15 deletion syndrome, isolated cases']",0060415,612513,261349,C4304538,,,,C567289,,,,
mondo:0012917,specific language impairment 4,"['specific language impairment 4', 'SLI4']",,612514,,C2675874,,,,C567288,,,,
mondo:0012918,primary ciliary dyskinesia 10,"['CILD10', 'primary ciliary dyskinesia 10 with or without situs inversus', 'DNAAF2 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 10, with or without situs inversus', 'ciliary dyskinesia, primary, type 10', 'primary ciliary dyskinesia type 10', 'ciliary dyskinesia, primary, 10', 'primary ciliary dyskinesia caused by mutation in DNAAF2']",0110612,612518,,C2675867,,,,C567287,,,,
mondo:0012919,type 1 diabetes mellitus 20,"['diabetes mellitus, insulin-dependent, type 20', 'diabetes mellitus, insulin-dependent, 20', 'IDDM20', 'type 1 diabetes mellitus caused by mutation in HNF1A', 'insulin-dependent diabetes mellitus 20', 'HNF1A type 1 diabetes mellitus']",0110757,612520,,C2675866,,,,C567286,,,,
mondo:0012920,type 1 diabetes mellitus 21,"['IDDM21', 'diabetes mellitus, insulin-dependent, 21', 'insulin-dependent diabetes mellitus 21']",0110758,612521,,C2675865,,,,C567285,,,,
mondo:0012921,type 1 diabetes mellitus 22,"['type 1 diabetes mellitus caused by mutation in CCR5', 'IDDM22', 'diabetes mellitus, insulin-dependent, 22', 'diabetes mellitus, insulin-dependent, type 22', 'CCR5 type 1 diabetes mellitus', 'insulin-dependent diabetes mellitus 22']",0110759,612522,,C2675864,,,,C567284,,,,
mondo:0012922,"pyloric stenosis, infantile hypertrophic, 5","['IHPS5', 'infantile hypertrophic pyloric stenosis type 5', 'pyloric stenosis, infantile hypertrophic, 5']",,612525,,C2675862,,,,C567283,,,,
mondo:0012923,congenital generalized lipodystrophy type 3,"['type 3 Berardinelli-Seip congenital lipodystrophy', 'CAV1 congenital generalised lipodystrophy (disease)', 'lipodystrophy, Berardinelli-Seip congenital, type 3', 'Berardinelli-Seip congenital lipodystrophy type 3', 'BSCL3', 'lipodystrophy, congenital generalized, type 3', 'CGL3', 'congenital generalised lipodystrophy (disease) caused by mutation in CAV1', 'CAV1 congenital generalized lipodystrophy (disease)', 'Berardinelli-Seip congenital lipodystrophy, type 3']",0111137,612526,,C2675861,,,,C567282,,,,
mondo:0012924,Diamond-Blackfan anemia 4,"['Diamond-Blackfan Anaemia type 4', 'Diamond-Blackfan Anemia type 4', 'Diamond-Blackfan anaemia caused by mutation in RPS17', 'Diamond-Blackfan anemia caused by mutation in RPS17', 'DBA4', 'Diamond-Blackfan anemia 4', 'RPS17 Diamond-Blackfan anemia', 'RPS17 Diamond-Blackfan anaemia']",0111890,612527,,C2675860,,C176913,,C567281,,,,
mondo:0012925,Diamond-Blackfan anemia 5,"['Diamond-Blackfan Anemia type 5', 'DBA5', 'Diamond-Blackfan anemia caused by mutation in RPL35A', 'RPL35A Diamond-Blackfan anemia', 'Diamond-Blackfan anaemia caused by mutation in RPL35A', 'Diamond-Blackfan anemia 5', 'RPL35A Diamond-Blackfan anaemia', 'Diamond-Blackfan Anaemia type 5']",0111883,612528,,C2675859,,C176914,,C567280,,,,
mondo:0012926,amelogenesis imperfecta hypomaturation type 2A2,"['amelogenesis imperfecta type IIA2', 'amelogenesis imperfecta, type IIA2', 'MMP20 amelogenesis imperfecta', 'amelogenesis imperfecta, hypomaturation type, IIA2', 'amelogenesis imperfecta caused by mutation in MMP20', 'amelogenesis imperfecta pigmented hypomaturation type 2', 'amelogenesis imperfecta, pigmented hypomaturation type, 2', 'amelogenesis imperfecta hypomaturation type IIA2', 'AI2A2']",0110060,612529,,C2675858,,,,C567279,,,,
mondo:0012927,chromosome 1q41-q42 deletion syndrome,"['monosomy 1q41-q42', 'chromosome 1q41-q42 deletion syndrome, isolated cases', '1q41q42 microdeletion syndrome', 'chromosome 1q41-q42 deletion syndrome', 'monosomy 1q41q42', 'deletion 1q41-q42', '1q41-q42 deletion syndrome', '1q41-q42 microdeletion syndrome', 'Del(1)(q41q42)', 'holoprosencephaly 10']",0060412,612530,250999,C4274528,,,,,,,,
mondo:0012928,hereditary spastic paraplegia 42,"['hereditary spastic paraplegia type 42', 'SPG42', 'autosomal dominant spastic paraplegia 42', 'SLC33A1 autosomal dominant pure spastic paraplegia', 'autosomal dominant spastic paraplegia type 42', 'spastic paraplegia 42, autosomal dominant', 'autosomal dominant pure spastic paraplegia caused by mutation in SLC33A1']",0110794,612539,171863,C2675528,"['-0.2717', '0.2274', '-0.456', '-0.1752', '-0.1017', '-0.887', '-0.4155', '0.11096', '-0.7573', '-0.4639', '-0.0903', '0.3047', '-0.10547', '0.2126', '0.911', '0.1973', '-0.2452', '-0.4048', '0.1526', '-0.5205', '0.1231', '-0.2957', '0.6104', '-0.1654', '-0.1655', '0.03029', '0.11884', '-0.11676', '-0.1417', '-0.2343', '0.382', '0.1553', '0.0862', '0.1028', '0.09906', '-0.2502', '-0.453', '-0.2175', '-0.00949', '-0.3313', '0.014046', '-0.7793', '-0.07336', '0.2365', '-0.1614', '-0.1896', '-0.351', '0.3633', '0.02559', '0.2186', '0.1465', '0.1759', '-0.7495', '-0.2637', '-0.3237', '-0.622', '0.5186', '-0.038', '-0.2595', '0.688', '-0.09686', '-0.3315', '0.1837', '0.2435', '-0.805', '0.36', '0.3884', '0.9517', '-0.302', '0.6675', '0.08496', '-0.0246', '0.09106', '-0.3054', '1.27', '0.2054', '-0.1138', '-0.1108', '-0.00318', '-0.605', '-0.2905', '-0.311', '0.9766', '1.085', '-0.1681', '0.1268', '-0.07684', '0.1576', '0.404', '-0.0777', '0.604', '0.1243', '-0.03653', '0.3882', '0.5615', '0.797', '0.7676', '0.4377', '-0.331', '-0.1381']",,,C567262,,,,
mondo:0012929,Compton-North congenital myopathy,"['myopathy, congenital, Compton-NORTH', 'MYPCN', 'congenital lethal myopathy, Compton-North type']",0080101,612540,210163,C2675527,"['-0.6807', '-0.01189', '0.02667', '-0.3894', '0.1256', '-0.451', '0.02283', '0.4058', '-0.4956', '-0.1444', '-0.4111', '0.1353', '0.05298', '-0.1062', '-0.1971', '0.148', '0.08234', '0.006756', '-0.2864', '-0.7744', '0.1573', '-0.1854', '0.4062', '0.1265', '0.0925', '-0.0743', '0.064', '-0.2102', '-0.0901', '-0.2827', '0.1154', '0.1969', '0.3372', '0.4014', '-0.10394', '-0.1753', '-0.1722', '0.004486', '-0.03775', '-0.1337', '-0.2037', '-0.2289', '-0.1377', '0.256', '-0.2325', '-0.1364', '-0.1724', '0.3086', '0.02084', '0.11743', '-0.2115', '-0.3528', '0.1937', '-0.2313', '-0.2944', '-0.3303', '0.2747', '-0.2556', '0.2036', '0.131', '0.2744', '-0.00901', '-0.1323', '-0.01776', '-0.366', '-0.12054', '0.322', '0.3467', '-0.5205', '0.019', '-0.0868', '0.1991', '0.0806', '-0.0132', '0.004063', '-0.2396', '0.04062', '0.001528', '-0.2013', '-0.01003', '0.1576', '0.3115', '-0.014084', '0.1678', '-0.1725', '0.2576', '0.01103', '0.47', '0.3318', '-0.2141', '0.3455', '0.3564', '0.2622', '0.1332', '0.1945', '0.3108', '0.5723', '-0.358', '0.2139', '0.1437']",,,C567261,,,,
mondo:0012930,autosomal recessive severe congenital neutropenia due to G6PC3 deficiency,"['SCN4', 'Dursun syndrome', 'neutropenia, severe congenital 4, autosomal recessive', 'severe congenital neutropenia-pulmonary hypertension-superficial venous angiectasis syndrome', 'severe congenital neutropenia type 4', 'neutropenia, severe congenital, 4, autosomal recessive', 'pulmonary arterial hypertension, leukopenia, and atrial septal defect']",0112136,612541,331176,C2675526,"['-0.4595', '0.0757', '0.5063', '-0.6323', '0.3699', '0.079', '0.2908', '0.06964', '-0.1665', '-0.2393', '0.0687', '-0.0708', '0.11383', '-0.3135', '-0.4436', '0.08264', '-0.207', '0.2426', '-0.332', '-0.502', '0.03464', '0.2952', '0.305', '-0.0927', '-0.1576', '-0.0674', '-0.03543', '0.04688', '0.379', '-0.4294', '0.077', '0.1577', '0.506', '0.313', '0.0764', '-0.27', '-0.1168', '-0.2896', '-0.345', '-0.5815', '-0.0989', '0.05292', '0.1484', '-0.1367', '-0.4875', '-0.09406', '0.1539', '0.3662', '0.1761', '0.1163', '-0.06033', '0.0713', '0.2742', '-0.01921', '-0.3696', '-0.2119', '-0.0256', '0.1658', '-0.1875', '0.279', '-0.0908', '0.2722', '-0.0742', '-0.1086', '0.315', '-0.343', '0.3428', '0.487', '-0.3901', '0.409', '-0.4543', '0.0916', '-0.0737', '0.1896', '-0.0809', '-0.0542', '0.473', '-0.2913', '-0.001008', '0.02177', '-0.243', '-0.1451', '0.1587', '0.2747', '-0.2433', '0.1925', '0.2817', '0.3086', '-0.0313', '-0.003326', '0.02847', '0.482', '0.162', '-0.02628', '0.8633', '0.6343', '0.7603', '-0.3484', '0.07196', '0.2585']",,,,,,,
mondo:0012931,"focal segmental glomerulosclerosis 4, susceptibility to","['focal segmental glomerulosclerosis caused by mutation in APOL1', 'FSGS4', 'susceptibility to focal segmental glomerulosclerosis 4', 'APOL1 focal segmental glomerulosclerosis', 'focal segmental glomerulosclerosis 4, susceptibility to', 'end-stage renal disease, nondiabetic, susceptibility to', 'glomerulosclerosis, focal segmental, 4, susceptibility to']",,612551,,,,,,,,,,
mondo:0012932,"myopia 16, autosomal dominant","['myopia 16, autosomal dominant', 'MYP16', 'myopia 16']",,612554,,C2675523,,,,C567259,,,,
mondo:0012933,"breast-ovarian cancer, familial, susceptibility to, 2","['breast-ovarian cancer, familial, susceptibility to, 2', 'hereditary breast ovarian cancer syndrome caused by mutation in BRCA2', 'ovarian cancer, familial, susceptibility to, 2', 'breast-ovarian cancer, familial, 2', 'breast cancer, familial, susceptibility to, 2', 'BRCA2 hereditary breast ovarian cancer syndrome', 'breast-ovarian cancer, familial, susceptibility to, type 2', 'susceptibility to familial breast-ovarian cancer 2', 'BROVCA2']",,612555,,,,,,,,,,
mondo:0012934,"leukemia, chronic lymphocytic, susceptibility to, 3","['leukemia, chronic lymphocytic, susceptibility to, type 3', 'leukemia, chronic lymphocytic, susceptibility to, 3', 'Clls3']",,612557,,,,,,,,,,
mondo:0012935,"leukemia, chronic lymphocytic, susceptibility to, 4","['leukemia, chronic lymphocytic, susceptibility to, 4', 'leukemia, chronic lymphocytic susceptibility to, 4', 'leukemia, chronic lymphocytic, susceptibility to, type 4', 'Clls4']",,612558,,,,,,,,,,
mondo:0012936,"leukemia, chronic lymphocytic, susceptibility to, 5","['Clls5', 'leukemia, chronic lymphocytic, susceptibility to, 5', 'leukemia, chronic lymphocytic, susceptibility to, type 5', 'leukemia, chronic lymphocytic susceptibility to, 5']",,612559,,,,,,,,,,
mondo:0012937,Diamond-Blackfan anemia 6,"['DBA6', 'RPL5 Diamond-Blackfan anaemia', 'RPL5 Diamond-Blackfan anemia', 'Diamond-Blackfan Anaemia type 6', 'Diamond-Blackfan anaemia caused by mutation in RPL5', 'Diamond-Blackfan anemia caused by mutation in RPL5', 'Aase-Smith syndrome 2', 'Diamond-Blackfan anemia 6', 'Diamond-Blackfan Anemia type 6']",0111879,612561,,,,C176915,,,,,,
mondo:0012938,Diamond-Blackfan anemia 7,"['Diamond-Blackfan Anaemia type 7', 'RPL11 Diamond-Blackfan anaemia', 'Diamond-Blackfan anemia caused by mutation in RPL11', 'Diamond-Blackfan anaemia caused by mutation in RPL11', 'Diamond-Blackfan Anemia type 7', 'RPL11 Diamond-Blackfan anemia', 'Diamond-Blackfan anemia 7', 'DBA7']",0111878,612562,,C2675512,,C176916,,C567254,,,,
mondo:0012939,Diamond-Blackfan anemia 8,"['Diamond-Blackfan anemia caused by mutation in RPS7', 'Diamond-Blackfan Anaemia type 8', 'Diamond-Blackfan anemia 8', 'RPS7 Diamond-Blackfan anaemia', 'DBA8', 'Diamond-Blackfan Anemia type 8', 'RPS7 Diamond-Blackfan anemia', 'Diamond-Blackfan anaemia caused by mutation in RPS7']",0111881,612563,,C2675511,,C176917,,C567253,,,,
mondo:0012940,inflammatory bowel disease 24,"['inflammatory bowel disease type 24', 'IBD24', 'inflammatory bowel disease 24']",0110908,612566,,C2675509,,,,C567252,,,,
mondo:0012941,inflammatory bowel disease 25,"['inflammatory bowel disease caused by mutation in IL10RB', 'early onset autosomal recessive inflammatory bowel disease 25', 'IBD25', 'inflammatory bowel disease type 25', 'inflammatory bowel disease 25, early onset, autosomal recessive', 'inflammatory bowel disease 25, autosomal recessive', 'inflammatory bowel disease, early-onset, autosomal recessive', 'IL10RB inflammatory bowel disease']",0110909,612567,,C2675508,,,,C567251,,,,
mondo:0012942,lung cancer susceptibility 3,"['lung cancer susceptibility 3', 'adenocarcinoma of lung, susceptibility to', 'LNCR3']",,612571,,C2675497,,,,,,,,
mondo:0012943,retinitis pigmentosa 46,"['retinitis pigmentosa 46', 'IDH3B retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in IDH3B', 'RP46', 'retinitis pigmentosa type 46', 'retinitis pigmentosa, autosomal recessive, Idh3B-related']",0110409,612572,,C2675496,,,,C567249,,H35.5,,
mondo:0012944,"chromosome 17P13.3, telomeric, duplication syndrome","['split-hand/foot malformation with long bone deficiency 3', 'chromosome 17P13.3, telomeric, duplication syndrome']",,612576,,C2675492,"['-0.0639', '0.0633', '0.01009', '-0.0351', '0.0844', '-0.1163', '-0.02182', '0.0917', '-0.094', '-0.0697', '-0.0345', '-0.00979', '0.03232', '0.01653', '-0.0224', '-0.04578', '0.00799', '-0.03662', '-0.0431', '-0.15', '0.02179', '-6e-06', '0.0893', '-0.03845', '0.0566', '-0.0293', '-0.0523', '0.01016', '0.05054', '-0.0641', '0.1023', '-0.01482', '0.1107', '0.02171', '0.06445', '-0.0589', '-0.02618', '-0.06824', '-0.01412', '-0.10333', '0.0334', '-0.07056', '0.002588', '-0.04462', '0.02287', '-0.1284', '-0.07837', '0.06744', '0.0563', '0.00993', '-0.0661', '-0.03568', '-0.04266', '0.0201', '-0.057', '-0.0362', '0.11414', '-0.02124', '-0.1227', '0.03087', '0.0346', '0.04056', '0.02516', '0.0419', '-0.0275', '0.01866', '0.0873', '0.06494', '-0.11816', '0.1077', '-0.12274', '0.02026', '0.05185', '-0.0636', '0.03076', '0.06616', '0.01662', '0.01083', '-0.0823', '-0.04587', '0.04196', '0.0603', '0.001856', '0.0703', '-0.02177', '-0.00853', '0.02383', '0.1415', '0.10974', '0.06058', '0.02165', '0.09845', '0.03232', '-0.01851', '0.2239', '0.00305', '0.08374', '-0.1736', '0.01904', '0.0562']",,,C567245,,,,
mondo:0012945,amyotrophic lateral sclerosis type 11,"['amyotrophic lateral sclerosis type 11', 'amyotrophic lateral sclerosis caused by mutation in FIG4', 'ALS11', 'FIG4 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis 11']",0060202,612577,,C2675491,,,,C567244,,,,
mondo:0012946,"intellectual disability, autosomal dominant 3","['mental retardation, autosomal dominant type 3', 'intellectual disability, autosomal dominant type 3', 'autosomal dominant non-syndromic intellectual disability 3', 'autosomal dominant non-syndromic intellectual disability caused by mutation in CDH15', 'autosomal dominant intellectual disability 3', 'autosomal dominant mental retardation 3', 'CDH15 autosomal dominant non-syndromic intellectual disability', 'mental retardation, autosomal dominant 3', 'MRD3', 'intellectual disability, autosomal dominant 3']",0070033,612580,,C2675488,,,,C567241,,,,
mondo:0012947,"intellectual disability, autosomal dominant 4","['autosomal dominant intellectual disability 4', 'KIRREL3 autosomal dominant non-syndromic intellectual disability', 'MRD4', 'intellectual disability, autosomal dominant 4', 'autosomal dominant non-syndromic intellectual disability 4', 'mental retardation, autosomal dominant type 4', 'autosomal dominant non-syndromic intellectual disability caused by mutation in KIRREL3', 'autosomal dominant mental retardation 4', 'mental retardation, autosomal dominant 4', 'intellectual disability, autosomal dominant type 4']",0070034,612581,,C2675487,,,,C567240,,,,
mondo:0012948,chromosome 6pter-p24 deletion syndrome,"['chromosome 6pter-p24 deletion syndrome', '6p25 microdeletion syndrome', 'chromosome 6pter-p24 deletion syndrome, isolated cases', 'distal monosomy type 6p', '6p subtelomeric deletion syndrome', 'distal deletion 6p', 'monosomy 6p25', 'distal monosomy 6p']",0060422,612582,96125,C4305276,,,,C567239,,,,
mondo:0012949,"aneurysm, intracranial berry, 9","['ANIB9', 'aneurysm, intracranial BERRY, 9']",0080972,612586,,C2675485,,,,C567238,,,,
mondo:0012950,"aneurysm, intracranial berry, 10","['aneurysm, intracranial BERRY, 10', 'ANIB10']",0080973,612587,,C2675484,,,,C567237,,,,
mondo:0012951,"colorectal cancer, susceptibility to, 8","['colorectal cancer, susceptibility to, 8', 'CRCS8', 'colorectal cancer, susceptibility to, on chromosome 14Q']",,612589,,,,,,,,,,
mondo:0012952,"colorectal cancer, susceptibility to, 9","['colorectal cancer, susceptibility to, on chromosome 16Q', 'colorectal cancer, susceptibility to, 9', 'CRCS9']",,612590,,,,,,,,,,
mondo:0012953,"colorectal cancer, susceptibility to, 10","['colorectal cancer, susceptibility to, 10', 'susceptibility to colorectal cancer 10', 'CRCS10', 'colorectal cancer, susceptibility to, type 10', 'colorectal cancer caused by mutation in POLD1', 'colorectal cancer, susceptibility to, on chromosome 19Q', 'POLD1 colorectal cancer']",,612591,,,,,,,,,,
mondo:0012954,"colorectal cancer, susceptibility to, 11","['colorectal cancer, susceptibility to, 11', 'colorectal cancer, susceptibility to, on chromosome 20P', 'CRCS11']",,612592,,,,,,,,,,
mondo:0012955,lung cancer susceptibility 4,"['LNCR4', 'lung cancer susceptibility 4']",,612593,,C2675479,,,,,,,,
mondo:0012956,"multiple sclerosis, susceptibility to, 2","['MS2', 'multiple sclerosis, susceptibility to, 2']",,612594,,,,,,,,,,
mondo:0012957,"multiple sclerosis, susceptibility to, 3","['multiple sclerosis, susceptibility to, 3', 'MS3']",,612595,,,,,,,,,,
mondo:0012958,"multiple sclerosis, susceptibility to, 4","['multiple sclerosis, susceptibility to, 4', 'MS4']",,612596,,,,,,,,,,
mondo:0012959,"psoriasis 11, susceptibility to","['psoriasis susceptibility 11', 'psoriasis 11, susceptibility to', 'PSORS11']",0111285,612599,,,,,,,,,,
mondo:0012960,"intellectual disability, autosomal dominant 5","['MRD5', 'intellectual disability, autosomal dominant type 5', 'autosomal dominant mental retardation 5', 'SYNGAP1-related non-syndromic intellectual disability', 'intellectual disability, autosomal dominant 5', 'autosomal dominant non-syndromic intellectual disability caused by mutation in SYNGAP1', 'SYNGAP1 autosomal dominant non-syndromic intellectual disability', 'SYNGAP1 Gene mutation linked to intellectual disability, schizophrenia and autism', 'autosomal dominant non-syndromic intellectual disability 5', 'mental retardation, autosomal dominant 5', 'SYNGAP1-related NSID', 'SYNGAP1 syndrome', 'autosomal dominant intellectual disability 5', 'mental retardation, autosomal dominant type 5']",0070035,612621,,C2675473,,,,C567234,,,,
mondo:0012961,type 1 diabetes mellitus 23,"['IDDM23', 'diabetes mellitus, insulin-dependent, 23', 'insulin-dependent diabetes mellitus 23']",0110760,612622,,C2675472,,,,C567233,,,,
mondo:0012962,"microvascular complications of diabetes, susceptibility to, 2","['microvascular complications of diabetes, susceptibility to, 2', 'MVCD2', 'microvascular complications of diabetes 2', 'microvascular complications of diabetes, susceptibility to, type 2', 'proliferative retinopathy, diabetic, susceptibility to', 'end-stage renal disease, diabetic, susceptibility to', 'EPO microvascular complications of diabetes, susceptibility', 'microvascular complications of diabetes, susceptibility caused by mutation in EPO']",,612623,,,,,,,,,,
mondo:0012963,"microvascular complications of diabetes, susceptibility to, 3","['microvascular complications of diabetes, susceptibility to, type 3', 'MVCD3', 'nephropathy, diabetic, susceptibility to', 'end-stage renal disease, diabetic, susceptibility to', 'microvascular complications of diabetes, susceptibility caused by mutation in ACE', 'microvascular complications of diabetes, susceptibility to, 3', 'ACE microvascular complications of diabetes, susceptibility', 'microvascular complications of diabetes 3']",,612624,,,,,,,,,,
mondo:0012964,chromosome 15q26-qter deletion syndrome,"['distal 15q deletion syndrome', 'distal monosomy 15q', 'distal monosomy type 15q', 'chromosome 15q26-qter deletion syndrome', '15q26 deletion syndrome', 'telomeric 15q deletion syndrome', 'Drayer syndrome', 'chromosome 15q26-qter deletion syndrome, isolated cases', 'monosomy 15q26']",0060397,612626,1596,C2675463,,,,C567232,,,,
mondo:0012965,"seizures, benign familial infantile, 4","['BFIS4', 'convulsions, benign familial infantile, 4', 'seizures, benign familial infantile, 4']",0081117,612627,,C2675462,,,,C567231,,,,
mondo:0012966,"microvascular complications of diabetes, susceptibility to, 4","['IL1RN microvascular complications of diabetes, susceptibility', 'microvascular complications of diabetes, susceptibility caused by mutation in IL1RN', 'microvascular complications of diabetes, susceptibility to, type 4', 'nephropathy, diabetic, susceptibility to', 'microvascular complications of diabetes 4', 'MVCD4', 'microvascular complications of diabetes, susceptibility to, 4']",,612628,,,,,,,,,,
mondo:0012967,hemolytic anemia due to adenylate kinase deficiency,"['ADENYLATE KINASE deficiency, hemolytic anaemia due to', 'ADENYLATE KINASE deficiency, hemolytic anemia due to']",,612631,86817,C2675459,"['-0.553', '0.3352', '-0.1432', '0.524', '0.611', '0.2239', '-0.3247', '0.4314', '-0.2988', '-0.3975', '0.825', '0.03458', '0.03613', '0.595', '-1.199', '0.1968', '-0.6353', '0.3206', '-0.7095', '-0.58', '-0.1952', '-0.4504', '0.3723', '-0.214', '0.6885', '-0.2795', '-0.007', '-0.3396', '0.65', '-0.01604', '0.1913', '0.05035', '0.503', '0.4912', '0.3552', '-0.4707', '-0.8203', '-0.591', '0.6367', '-0.4304', '-0.649', '0.2625', '0.05298', '-0.1315', '-0.6675', '-0.883', '0.1843', '0.1409', '0.2793', '-0.1986', '0.3574', '0.4624', '0.757', '-0.0906', '0.38', '-0.7095', '0.010895', '0.4832', '-1.012', '0.2708', '0.0352', '0.1758', '-0.428', '-0.2211', '-0.1512', '0.2795', '0.2162', '0.9907', '-0.6016', '0.778', '0.8535', '-0.2627', '-0.673', '-0.564', '0.2544', '1.105', '0.3616', '0.2893', '0.06464', '0.248', '0.1498', '-0.2153', '0.09033', '0.12415', '0.5015', '-0.279', '-0.5166', '0.363', '0.815', '-0.3113', '0.6416', '0.2573', '-0.3188', '-0.1241', '0.6553', '1.213', '0.1218', '-0.0469', '0.2888', '-0.4802']",,,C567228,,,,
mondo:0012968,Usher syndrome type 1H,"['Usher syndrome type IH', 'USH1H', 'USHER syndrome, type IH', 'Usher syndrome, type 1H']",0110835,612632,,C2675458,,,,C567227,,H35.5,,
mondo:0012969,"microvascular complications of diabetes, susceptibility to, 5","['PON1 microvascular complications of diabetes, susceptibility', 'microvascular complications of diabetes, susceptibility caused by mutation in PON1', 'microvascular complications of diabetes 5', 'MVCD5', 'retinopathy, diabetic, susceptibility to', 'microvascular complications of diabetes, susceptibility to, 5', 'microvascular complications of diabetes, susceptibility to, type 5']",,612633,,,,,,,,,,
mondo:0012970,"microvascular complications of diabetes, susceptibility to, 6","['microvascular complications of diabetes, susceptibility caused by mutation in SOD2', 'microvascular complications of diabetes, susceptibility to, type 6', 'nephropathy, diabetic, susceptibility to', 'microvascular complications of diabetes 6', 'MVCD6', 'microvascular complications of diabetes, susceptibility to, 6', 'SOD2 microvascular complications of diabetes, susceptibility']",,612634,,,,,,,,,,
mondo:0012971,"microvascular complications of diabetes, susceptibility to, 7","['microvascular complications of diabetes, susceptibility to, type 7', 'proliferative retinopathy, diabetic, susceptibility to', 'nephropathy, diabetic, susceptibility to', 'HFE microvascular complications of diabetes, susceptibility', 'nonproliferative retinopathy, diabetic, susceptibility to', 'microvascular complications of diabetes 7', 'MVCD7', 'microvascular complications of diabetes, susceptibility caused by mutation in HFE', 'microvascular complications of diabetes, susceptibility to, 7']",,612635,,,,,,,,,,
mondo:0012972,"febrile seizures, familial, 10","['convulsions, familial febrile, 10', 'FEB10', 'febrile seizures, familial, 10']",0111304,612637,,C2675251,,,,C567218,,,,
mondo:0012973,inflammatory bowel disease 26,"['IBD26', 'inflammatory bowel disease type 26', 'inflammatory bowel disease 26']",0110901,612639,,C2675249,,,,C567217,,,,
mondo:0012974,autosomal dominant nonsyndromic hearing loss 59,"['autosomal dominant nonsyndromic deafness type 59', 'DFNA59', 'autosomal dominant deafness 59', 'autosomal dominant nonsyndromic deafness 59', 'deafness, autosomal dominant 59']",0110583,612642,,C2675238,,,,C567216,,,,
mondo:0012975,autosomal dominant nonsyndromic hearing loss 3B,"['deafness, autosomal dominant type 3B', 'GJB6 autosomal dominant nonsyndromic deafness', 'DFNA3B', 'deafness, autosomal dominant 3b', 'autosomal dominant deafness 3B', 'autosomal dominant nonsyndromic deafness type 3B', 'autosomal dominant nonsyndromic deafness 3B', 'autosomal dominant nonsyndromic deafness caused by mutation in GJB6', 'deafness, autosomal dominant 3B']",0110565,612643,,C2675237,,,,C567215,,,,
mondo:0012976,autosomal dominant nonsyndromic hearing loss 2B,"['autosomal dominant deafness 2B', 'deafness, autosomal dominant type 2B', 'autosomal dominant nonsyndromic deafness type 2B', 'autosomal dominant nonsyndromic deafness caused by mutation in GJB3', 'deafness, autosomal dominant 2B', 'DFNA2B', 'deafness, autosomal dominant 2b', 'autosomal dominant nonsyndromic deafness 2B', 'GJB3 autosomal dominant nonsyndromic deafness']",0110559,612644,,C2675236,,,,C567214,,,,
mondo:0012977,autosomal recessive nonsyndromic hearing loss 1B,"['deafness, autosomal recessive type 1B', 'GJB6 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 1B', 'DFNB1B', 'autosomal recessive deafness 1B', 'deafness, autosomal recessive 1B', 'deafness, autosomal recessive 1b', 'autosomal recessive nonsyndromic deafness caused by mutation in GJB6', 'Autosomal recessive deafness type 1B', 'autosomal recessive nonsyndromic deafness 1B']",0110476,612645,,CN674504,,,,C567213,,,,
mondo:0012978,primary ciliary dyskinesia 11,"['primary ciliary dyskinesia caused by mutation in RSPH4A', 'ciliary dyskinesia, primary, 11, without situs inversus', 'CILD11', 'ciliary dyskinesia, primary, type 11', 'primary ciliary dyskinesia 11 without situs inversus', 'RSPH4A primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 11', 'primary ciliary dyskinesia type 11']",0110602,612649,,C2675229,,,,C567212,,,,
mondo:0012979,primary ciliary dyskinesia 12,"['primary ciliary dyskinesia 12 without situs inversus', 'primary ciliary dyskinesia type 12', 'primary ciliary dyskinesia caused by mutation in RSPH9', 'RSPH9 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 12, without situs inversus', 'ciliary dyskinesia, primary, type 12', 'ciliary dyskinesia, primary, 12', 'CILD12']",0110601,612650,,C2675228,,,,C567211,,,,
mondo:0012980,endocrine-cerebro-osteodysplasia syndrome,"['ECO syndrome', 'endocrine-CEREBROOSTEODYSPLASIA', 'ECO']",0060641,612651,199332,C4509819,"['-0.1978', '0.2191', '0.2345', '-0.1578', '0.1653', '0.09644', '-0.3374', '0.1814', '-0.2993', '-0.912', '-0.767', '-0.3242', '-0.2585', '0.1127', '-0.4033', '0.2583', '0.1731', '-0.1332', '-0.8716', '-0.2947', '0.1776', '-0.335', '0.4565', '-0.398', '0.3906', '-0.2094', '-0.4243', '-0.218', '0.7407', '-0.7476', '0.4468', '0.02136', '0.157', '-0.4006', '0.332', '-0.05737', '-0.2751', '-0.3408', '-0.1993', '-0.3494', '-0.2607', '-0.397', '-0.10175', '-0.4172', '0.3657', '-0.6167', '0.4905', '0.4817', '-0.2625', '-0.1644', '-0.3123', '-0.2722', '-0.1112', '0.3296', '-0.3506', '-0.8696', '0.04465', '-0.07776', '0.528', '0.6006', '0.2397', '-0.1653', '-0.2231', '-0.161', '-0.2507', '0.2664', '0.101', '0.7905', '-0.7754', '-0.0626', '-0.3176', '0.2903', '0.1504', '0.4045', '-0.4614', '0.4067', '0.0877', '0.1016', '0.04453', '0.1135', '-0.223', '0.3433', '0.5317', '0.531', '0.2944', '0.10333', '0.2338', '0.618', '0.3843', '-0.3516', '-0.3137', '0.2598', '0.2025', '-0.679', '0.694', '0.3953', '0.6777', '-0.4636', '0.1692', '0.4336']",,,C567210,,,,
mondo:0012981,hereditary spherocytosis type 4,"['HS4', 'hereditary spherocytosis caused by mutation in SLC4A1', 'SLC4A1 hereditary spherocytosis', 'SPH4', 'hereditary spherocytosis 4', 'spherocytosis, type 4', 'spherocytosis, hereditary, 4']",0110919,612653,,C2675212,,,,C567208,,,,
mondo:0012982,episodic ataxia type 6,"['hereditary episodic ataxia caused by mutation in SLC1A3', 'SLC1A3 hereditary episodic ataxia', 'EA6', 'episodic ataxia, type 6']",0050994,612656,209967,C2675211,"['-0.226', '-0.1735', '-0.00527', '0.0521', '-0.2496', '-0.608', '0.1769', '-0.10645', '-0.7065', '-0.857', '0.09393', '0.2163', '-0.2306', '0.3142', '0.4644', '-0.3186', '-0.0938', '-0.2554', '0.0408', '-0.7173', '-0.1755', '-0.2493', '0.1964', '-0.723', '0.5854', '-0.57', '-0.3013', '0.05777', '-0.1006', '-0.946', '-0.0966', '0.4692', '-0.4202', '-0.2886', '0.3472', '0.1853', '-0.1863', '0.08673', '0.2979', '0.37', '0.3267', '-0.02402', '-0.4055', '0.4817', '0.421', '-0.55', '0.11816', '0.2367', '0.2646', '0.0993', '-0.2822', '0.218', '-0.1836', '-0.4675', '-0.1941', '-0.6494', '0.0869', '0.501', '-0.0989', '0.469', '-0.6455', '0.16', '0.31', '-0.2118', '-0.3884', '0.568', '0.2693', '0.3926', '-0.4858', '0.58', '0.87', '0.719', '-0.0629', '-1.021', '0.849', '0.4204', '0.4438', '0.375', '0.1417', '0.4458', '-0.265', '-0.928', '0.3662', '0.7695', '0.01651', '-0.956', '0.2291', '0.04752', '0.5547', '0.413', '0.316', '0.502', '0.248', '0.1713', '1.119', '1.056', '0.4185', '0.3403', '-0.2776', '-0.06885']",,,C567207,,,,
mondo:0012983,cone-rod dystrophy 12,"['cone-rod dystrophy caused by mutation in PROM1', 'cone-rod dystrophy type 12', 'PROM1 cone-rod dystrophy', 'CORD12', 'cone-rod dystrophy 12']",0111019,612657,,C2675210,,,,C567206,,,,
mondo:0012984,PHARC syndrome,"['polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract', 'PHARC syndrome', 'polyneuropathy-hearing loss-ataxia-retinitis pigmentosa-cataract syndrome', 'PHARC', 'peripheral neuropathy, Fiskerstrand type', 'polyneyropathy, hearing loss, ataxia, retinitis pigmentosa, and cataract']",0080181,612674,171848,C2675204,"['-0.7617', '0.695', '0.1602', '0.03397', '0.04092', '-1.171', '-0.962', '1.165', '-0.487', '-0.0904', '-0.708', '0.1742', '0.348', '0.04205', '0.3313', '-0.3687', '-0.1604', '0.2006', '0.1247', '-0.254', '-0.02953', '-0.4153', '0.1398', '0.058', '-0.00892', '0.1575', '-0.5654', '0.4067', '-0.4172', '-0.2605', '0.2727', '-0.1945', '-0.2764', '0.3042', '-0.4348', '-0.6997', '-0.2118', '-0.5054', '-0.03864', '-0.2496', '-0.365', '-0.05994', '0.2405', '0.624', '-0.03735', '-0.3184', '0.06915', '0.1404', '-0.5103', '-0.02747', '0.167', '0.5713', '0.1265', '-0.2979', '0.5996', '-0.777', '1.129', '-0.3782', '-0.06885', '0.0867', '-0.01167', '0.07935', '0.833', '0.537', '-0.5977', '0.513', '0.4185', '0.4175', '-0.417', '-0.1757', '-0.2515', '0.451', '-0.194', '-0.3289', '0.4246', '-0.1381', '0.0004594', '0.04373', '0.2003', '0.1823', '-0.101', '0.7197', '0.0809', '0.3582', '-0.0358', '0.04855', '0.1464', '0.1887', '0.115', '0.12256', '0.6514', '0.569', '0.10114', '0.03177', '0.362', '-0.0694', '0.2141', '-0.479', '-0.1722', '0.2896']",,,C567203,,,,
mondo:0012985,hereditary spherocytosis type 5,"['spherocytosis, type 5', 'hereditary spherocytosis caused by mutation in EPB42', 'hereditary spherocytosis 5', 'EPB42 hereditary spherocytosis', 'spherocytosis, hereditary, 5', 'SPH5', 'HS5']",0110920,612690,,C2675192,,,,C567202,,,,
mondo:0012986,bilateral parasagittal parieto-occipital polymicrogyria,"['polymicrogyria, bilateral temporooccipital', 'BTOP']",0080923,612691,208441,C2675191,"['-0.05728', '0.06854', '0.03986', '-0.01654', '0.0322', '-0.07526', '0.012634', '0.0595', '-0.0769', '-0.0529', '-0.06058', '-0.0474', '-0.03177', '-0.01567', '-0.03342', '-0.01126', '0.0264', '-0.08417', '-0.0358', '-0.1432', '-0.009605', '-0.03238', '0.06445', '-0.02425', '0.02731', '-0.03137', '-0.01235', '0.02512', '0.003485', '-0.0333', '0.04626', '-0.01524', '0.1013', '0.02197', '0.04257', '-0.01441', '-0.01214', '-0.014595', '-0.005577', '-0.0858', '0.0404', '-0.0625', '-0.00457', '-0.04596', '0.003176', '-0.04547', '-0.02719', '0.0804', '-0.011', '0.04233', '-0.01453', '-0.014786', '0.002363', '-0.01219', '-0.0759', '0.010864', '0.057', '-0.0577', '-0.111', '0.02008', '0.0516', '-0.001001', '-0.00784', '0.03693', '-0.0455', '-0.012245', '0.1038', '0.07294', '-0.0777', '0.0846', '-0.0686', '0.04596', '0.0659', '-0.01987', '0.01721', '0.02411', '0.04752', '-0.01558', '-0.0462', '-0.06647', '-0.03122', '-0.0002103', '0.0222', '0.0885', '-0.02133', '-0.0361', '-0.02173', '0.0867', '0.03516', '0.02406', '-0.004074', '0.1099', '0.0312', '0.03992', '0.1602', '-0.000267', '0.09064', '-0.0952', '0.02162', '0.04706']",,,C567201,,,,
mondo:0012987,"agammaglobulinemia 6, autosomal recessive","['autosomal agammaglobulinemia caused by mutation in CD79B', 'AGM6', 'agammaglobulinemia 6, autosomal recessive', 'CD79B autosomal agammaglobulinemia', 'agammaglobulinemia, autosomal recessive, due to Cd79B defect']",0081138,612692,,C3150207,,,,,,,,
mondo:0012988,hypogonadotropic hypogonadism 6 with or without anosmia,"['hypogonadotropic hypogonadism caused by mutation in FGF8', 'hypogonadotropic hypogonadism 6 with or without anosmia', 'FGF8 hypogonadotropic hypogonadism', 'Kallmann syndrome 6', 'HH6', 'KAL6']",0090086,612702,,C3552574,,,,C567199,,E23.0,,
mondo:0012989,"microcephaly 7, primary, autosomal recessive","['autosomal recessive primary microcephaly caused by mutation in STIL', 'microcephaly 7, primary, autosomal recessive', 'MCPH7', 'STIL autosomal recessive primary microcephaly']",0070278,612703,,C2675187,,,,C567198,,,,
mondo:0012990,Leber congenital amaurosis 13,"['retinitis pigmentosa 53', 'Leber congenital amaurosis type 13', 'RDH12 Leber congenital amaurosis', 'Leber congenital amaurosis caused by mutation in RDH12', 'LCA13', 'Leber congenital amaurosis 13']",0110330,612712,,C2675186,,,,C567197,,H35.5,,
mondo:0012991,Kahrizi syndrome,"['mental retardation, cataract, coloboma, and kyphosis, autosomal recessive', 'intellectual disability, cataract, coloboma, and kyphosis, autosomal recessive', 'KHRZ', 'Kahrizi syndrome']",0050807,612713,168972,CN200191,"['0.00343', '0.01235', '0.001908', '0.001771', '0.00953', '-0.02533', '-0.003654', '0.02264', '-0.006706', '-0.01522', '-0.005238', '0.002682', '0.011665', '-0.003824', '0.004528', '-0.01523', '-0.005672', '0.002663', '7.23e-05', '-0.0168', '0.006718', '-0.0001996', '0.01482', '-0.00582', '0.01144', '-0.006046', '-0.007523', '-0.00558', '-0.0002217', '-0.01272', '0.02167', '-0.00459', '0.0253', '0.01208', '0.01006', '-0.01092', '0.00212', '-0.003235', '-0.01213', '-0.013016', '0.00691', '-0.005203', '-0.004295', '0.001298', '0.01456', '-0.01132', '0.0003908', '0.001974', '-0.0006423', '-0.001826', '-0.0006537', '-0.00929', '-0.00557', '-0.00922', '-0.006767', '-0.01305', '0.002039', '-6.91e-05', '-0.01735', '0.002518', '0.011894', '-0.002857', '-0.00865', '0.000914', '-0.00909', '-0.003828', '0.01958', '0.01116', '-0.01949', '0.01619', '-0.007027', '0.00311', '0.005356', '-0.0086', '0.013145', '0.01289', '0.002752', '-0.00565', '-0.008865', '-0.00976', '0.004326', '-0.0009007', '-0.01313', '0.02475', '-0.010056', '-0.004', '-0.00384', '0.02423', '0.02141', '0.002922', '0.002857', '0.01678', '0.01585', '0.01172', '0.03114', '0.01295', '0.001859', '-0.01997', '-0.01313', '-0.003557']",,,C567196,,,,
mondo:0012992,pancreatic insufficiency-anemia-hyperostosis syndrome,"['exocrine pancreatic insufficiency, dyserythropoietic anemia, and calvarial hyperostosis']",,612714,199337,C4302747,"['-0.318', '0.3901', '-0.1707', '0.3823', '0.938', '0.11865', '-0.2488', '0.532', '-0.3867', '-0.594', '0.851', '-0.1233', '0.1615', '0.4932', '-1.076', '0.06073', '-0.695', '0.4116', '-0.706', '-0.3389', '-0.2954', '-0.3591', '0.257', '-0.1488', '0.6133', '-0.3523', '-0.07324', '-0.1644', '0.6777', '-0.0822', '0.1931', '0.236', '0.6543', '0.3232', '0.1758', '-0.3904', '-0.933', '-0.762', '0.3467', '-0.312', '-0.8936', '0.2612', '-0.02269', '-0.565', '-0.691', '-1.093', '0.4602', '0.1609', '0.4163', '-0.4517', '0.4885', '0.3738', '0.8726', '-0.06665', '0.48', '-1.161', '0.1763', '0.5273', '-1.074', '0.315', '-0.0712', '0.3252', '-0.2084', '-0.2593', '-0.2937', '0.2612', '0.1548', '0.7793', '-0.563', '0.6772', '0.753', '-0.3188', '-0.3928', '-0.503', '0.1667', '1.028', '0.00944', '0.3643', '0.0817', '0.8647', '0.1026', '0.04877', '-0.002165', '0.0721', '0.506', '-0.3113', '-0.4475', '0.5337', '0.8916', '-0.2103', '0.4905', '0.4153', '-0.1014', '-0.03812', '0.8364', '0.8535', '0.1498', '-0.1605', '0.226', '-0.659']",,,C567195,,,,
mondo:0012993,dyschromatosis universalis hereditaria 2,"['DUH2', 'dyschromatosis universalis hereditaria 2']",,612715,,C2675183,,,,C567194,,,,
mondo:0012994,dopa-responsive dystonia due to sepiapterin reductase deficiency,"['dopa-responsive dystonia due to sepiapterin reductase deficiency', 'sepiapterin reductase deficiency', 'SRD', 'SPR deficiency', 'dystonia, DOPA-responsive, due to sepiapterin reductase deficiency', 'DYT-SPR', 'autosomal recessive sepiapterin reductase-deficient DRD', 'DRD due to SRD']",0111168,612716,70594,C0268468,"['0.4688', '0.139', '0.02823', '-0.416', '-0.3462', '-0.6934', '-0.00895', '0.396', '-0.7812', '-0.2605', '0.5845', '0.974', '0.006046', '0.5825', '0.279', '0.7124', '-0.1398', '-0.7544', '-0.633', '-1.081', '-0.526', '-0.2294', '0.02243', '-0.02812', '-0.5996', '0.291', '-0.04922', '0.0786', '-0.328', '-0.004936', '0.08813', '0.3508', '0.941', '0.4207', '0.10205', '0.1914', '0.515', '-0.1747', '0.1947', '-0.2595', '0.4329', '-0.1277', '-0.3003', '0.3792', '0.4412', '0.01987', '-0.3281', '0.335', '0.05298', '0.7485', '0.1621', '0.0186', '0.4531', '-0.0868', '0.6064', '0.1595', '0.09186', '0.3164', '0.005882', '0.0816', '-0.7344', '-0.345', '-0.01258', '-0.651', '-0.6694', '0.1903', '0.09656', '0.3364', '-0.1764', '0.4543', '-0.4316', '-0.1302', '-0.1299', '-0.2217', '0.4844', '0.3655', '0.7905', '-0.5566', '-0.05585', '-0.3518', '-0.01663', '0.0673', '0.0657', '0.7266', '1.061', '0.0668', '0.01017', '0.2234', '1.61', '-0.00861', '0.7227', '0.2146', '0.0959', '0.07916', '0.65', '-0.01872', '-0.3933', '0.04144', '1.03', '-0.3538']",,,C562657,277.89,,,
mondo:0012995,"myopia 15, autosomal dominant","['MYP15', 'myopia 15, autosomal dominant']",,612717,,C2675180,,,,C567193,,,,
mondo:0012996,AGAT deficiency,"['disorder of glycine amidinotransferase activity', 'glycine amidinotransferase activity disease', 'cerebral creatine deficiency syndrome type 3', 'AGAT deficiency', 'L-arginine:glycine amidinotransferase deficiency', 'cerebral creatine deficiency syndrome 3', 'creatine deficiency syndrome due to AGAT deficiency', 'GATM deficiency', 'CCDS3', 'arginine:glycine amidinotransferase deficiency']",0050712,612718,35704,C2675179,"['-0.17', '-0.1284', '0.1412', '-0.2559', '-0.01427', '-0.404', '0.01814', '0.5576', '-0.2837', '-0.4316', '-0.2451', '-0.07367', '0.0828', '0.0453', '0.03482', '-0.0893', '-0.12036', '-0.02467', '-0.444', '-0.7495', '0.2446', '-0.11847', '0.01611', '0.08276', '0.183', '-0.2355', '-0.02135', '-0.394', '-0.2927', '-0.2126', '0.289', '-0.1991', '0.3323', '0.405', '-0.222', '-0.09485', '-0.2185', '-0.5', '0.08136', '0.2017', '0.2517', '-0.581', '0.0525', '0.1189', '-0.01123', '-0.1512', '-0.0469', '0.149', '-0.3118', '0.1333', '-0.1234', '-0.03043', '0.0917', '0.1298', '0.1184', '0.0804', '0.1632', '-0.4104', '-0.0271', '0.521', '-0.01506', '0.1149', '0.3206', '-0.2106', '0.0455', '-0.03662', '-0.04303', '0.5186', '-0.4553', '-0.0743', '0.00672', '0.2534', '-0.453', '-0.3591', '0.2301', '0.334', '0.02551', '-0.4126', '-0.1962', '0.2085', '0.5947', '0.3196', '0.1059', '0.2627', '0.4307', '0.2825', '-0.2656', '0.134', '0.7466', '0.1887', '0.5996', '0.3127', '-0.2339', '0.009575', '0.4175', '0.655', '0.1642', '-0.02322', '0.381', '-0.01675']",,,C567192,270.8,,,
mondo:0012997,cholestasis-pigmentary retinopathy-cleft palate syndrome,"['HARDIKAR syndrome', 'Hardikar syndrome']",,612726,1415,C0795969,,,,C535632,,,,
mondo:0012998,faciocardiomelic syndrome,['faciocardiomelic syndrome'],,612731,,C2674798,,,,C567176,,,,
mondo:0012999,guanidinoacetate methyltransferase deficiency,"['CCDS2', 'guanidinoacetate methyltransferase deficiency', 'GAMT deficiency', 'guanidinoacetate N-methyltransferase activity disease', 'disorder of guanidinoacetate N-methyltransferase activity', 'cerebral creatine deficiency syndrome 2', 'creatine deficiency syndrome due to GAMT deficiency', 'cerebral creatine deficiency syndrome type 2']",0050799,612736,382,C0574080,"['0.5874', '0.0485', '-0.2085', '-0.2129', '0.4685', '-0.3872', '0.1046', '0.4434', '-0.8965', '-0.1792', '-0.501', '0.272', '0.563', '-0.10175', '-0.01216', '0.0841', '0.139', '-0.4634', '-0.9595', '-0.763', '0.312', '-0.3342', '0.04657', '-0.01703', '0.4805', '-0.1703', '-0.2435', '-0.531', '-0.4612', '-0.06573', '0.291', '0.213', '0.601', '0.2612', '-0.1007', '-0.3035', '-0.0703', '-0.2876', '-0.10583', '0.286', '0.1251', '-0.713', '0.1853', '0.10876', '0.4587', '-0.6235', '0.4238', '0.2137', '-0.1577', '0.3665', '-0.5146', '0.3367', '-0.07135', '-0.2266', '0.2444', '0.1241', '0.1636', '-0.04742', '-0.1593', '0.805', '0.0254', '0.4434', '0.6694', '-0.2439', '-0.4626', '-0.2003', '0.1512', '-0.0857', '-0.2703', '-0.3545', '0.1037', '0.4246', '-0.589', '0.0671', '0.1832', '0.4404', '0.3152', '-0.479', '-0.3606', '-0.1815', '0.2355', '-0.0373', '0.05548', '0.5454', '0.2932', '0.2285', '-0.2152', '0.1981', '0.64', '0.42', '0.1371', '0.858', '-0.2433', '-0.5967', '0.02153', '0.576', '0.11816', '-0.4617', '0.473', '0.134']",,,C537622,277.6,,,
mondo:0013000,porphyria due to ALA dehydratase deficiency,"['ALA dehydratase deficiency pophyria', 'porphyria, ALAD', 'ALAD porphyria', 'porphyria due to delta-aminolevulinate dehydratase deficiency', 'porphyria due to ALAD deficiency', 'ALAD deficiency', 'acute hepatic porphyria', 'porphobilinogen synthase deficiency', 'porphyria of Doss', 'Doss porphyria', 'Lead poisoning, susceptibility to', 'aminolevulinate dehydratase deficiency porphyria', '5-aminolevulinic acid dehydratase deficiency porphyria', 'porphyria, acute hepatic', 'Delta-aminolevulinate dehydratase deficiency']",,612740,100924,,"['0.02798', '-0.4302', '-0.8447', '-0.443', '-0.1768', '-0.3662', '0.03387', '-0.03029', '-0.773', '-0.1875', '-0.2776', '0.352', '-0.0266', '1.425', '-0.7896', '-0.1859', '0.5537', '0.2211', '-0.603', '-0.635', '-0.2397', '-0.3445', '-0.12115', '-0.4258', '0.1373', '-0.8657', '-0.234', '-0.1083', '0.4856', '-0.853', '-0.1581', '-0.548', '0.863', '-0.9805', '-0.1317', '-0.6035', '-0.508', '0.0714', '0.11664', '-0.0083', '0.12085', '-0.4834', '-0.1937', '-0.3826', '-0.06537', '-0.6235', '0.4307', '-0.592', '1.018', '0.1114', '-0.1102', '0.4856', '0.942', '0.065', '-0.244', '-0.1593', '-0.07916', '0.0878', '0.001293', '-0.2428', '0.09973', '-0.2219', '1.137', '-0.11945', '-0.4333', '0.703', '-0.0828', '0.6284', '0.4226', '-0.0744', '-0.795', '-0.1143', '0.2269', '-0.806', '0.4028', '0.9155', '0.3823', '0.175', '0.1267', '-0.4036', '0.2369', '-0.4558', '0.1285', '-0.481', '0.7476', '0.612', '1.163', '0.3098', '-0.00974', '0.2079', '0.7754', '-0.05002', '-0.7056', '0.6084', '0.4746', '1.193', '0.02052', '-0.7217', '0.2913', '0.3628']",C133887,,C562618,,,,
mondo:0013002,cone-rod dystrophy 9,"['CORD9', 'ADAM9 cone-rod dystrophy', 'cone-rod dystrophy type 9', 'cone-rod dystrophy 9', 'cone-rod dystrophy caused by mutation in ADAM9']",0111020,612775,,C1423873,,,,,,,,
mondo:0013003,isolated congenital hypoglossia/aglossia,"['hypoglossia with situs inversus', 'hypoglossia, isolated']",,612776,141152,C2748587,,,,,,,,
mondo:0013004,"hypotonia, seizures, and precocious puberty","['hypotonia, seizures, and precocious puberty']",,612777,,C2748586,,,,C567566,,,,
mondo:0013005,EAST syndrome,"['seizures, sensorineural deafness, ataxia, mental retardation and electrolyte imbalance', 'SESAMES', 'sesame syndrome', 'seizures-sensorineural deafness-ataxia-intellectual disability-electrolyte imbalance syndrome', 'EAST syndrome', 'seizures, sensorineural deafness, ataxia, intellectual disability, and electrolyte imbalance', 'seizures - sensorineural deafness - ataxia - intellectual disability - electrolyte imbalance', 'epilepsy, ataxia, sensorineural deafness, and tubulopathy', 'epilepsy, ataxia, sensorineural deafness and tubulopathy', 'seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance', 'seizures, sensorineural deafness, ataxia, intellectual disability and electrolyte imbalance']",0060484,612780,199343,C2748572,"['-0.278', '0.1667', '-0.06616', '-0.611', '-0.2568', '-0.3716', '-0.2129', '0.7456', '-0.371', '-0.2715', '-0.6045', '-0.3645', '-0.2319', '-0.1952', '0.4592', '-0.1267', '0.08044', '-0.2542', '-0.1934', '-0.347', '0.4001', '-0.2637', '-0.1373', '-0.1263', '0.6226', '-0.09326', '-0.1344', '-0.0119', '-0.11566', '-0.1804', '-0.1554', '0.1425', '0.2205', '-0.0853', '-0.617', '-0.4492', '-0.2808', '-0.2856', '-0.3616', '-0.2223', '-0.51', '-0.0509', '0.481', '0.02496', '0.0791', '-0.286', '-0.159', '0.2461', '-0.1796', '0.02007', '-0.362', '0.3696', '-0.1124', '-0.2181', '0.3245', '0.1483', '0.7476', '-0.2766', '-0.274', '0.3015', '0.31', '0.1512', '-0.0577', '0.2046', '-0.643', '-0.05502', '-0.1724', '0.3628', '-0.3367', '0.428', '-0.55', '0.375', '0.2769', '0.02864', '0.2147', '0.2603', '0.904', '0.306', '0.1979', '0.1656', '0.2499', '0.1667', '0.264', '0.4385', '0.015175', '0.3567', '0.3606', '0.504', '0.04846', '0.3245', '0.2683', '0.508', '0.0316', '-0.1748', '0.7026', '0.2915', '0.5576', '-0.1567', '-0.06964', '0.515']",,,C557674,,,,
mondo:0013006,isolated growth hormone deficiency type IB,"['congenital isolated GH deficiency type IB', 'isolated growth hormone deficiency, type IB', 'isolated growth hormone deficiency type 1B', 'growth hormone deficiency, isolated, type IB', 'IGHD IB', 'IGHD1B', 'dwarfism of Sindh', 'congenital IGHD type IB', 'congenital isolated growth hormone deficiency type IB', 'IGHD 1B', 'isolated Growth hormone deficiency, type 1B']",0060874,612781,231671,C2748571,"['-0.6533', '0.11597', '0.01177', '-0.0355', '0.7036', '0.00703', '0.01689', '0.289', '-0.2622', '-0.2148', '-0.01956', '-0.00494', '0.3096', '-0.03424', '0.2246', '0.0957', '0.2498', '0.0542', '-0.4355', '-0.526', '-0.05405', '-0.2156', '0.1544', '-0.2588', '0.2131', '0.0194', '-0.1072', '-0.1809', '-0.2311', '-0.3794', '0.5093', '0.1315', '0.0742', '-0.0733', '-0.1544', '-0.03943', '-0.10425', '0.01405', '-0.1958', '-0.2512', '0.364', '-0.0505', '0.1586', '-0.08026', '-0.1407', '-0.3552', '0.228', '0.02104', '0.02373', '0.03262', '0.0917', '-0.4417', '-0.1254', '0.3347', '-0.21', '-0.084', '0.2585', '-0.2827', '-0.2461', '0.2678', '0.1925', '0.1019', '-0.04132', '-0.2455', '-0.06854', '0.1471', '0.1608', '0.1356', '-0.4092', '0.01772', '-0.209', '-0.0486', '0.1595', '-0.2443', '0.2998', '0.1172', '-0.0921', '-0.1155', '-0.03111', '-0.11743', '0.0725', '0.3003', '-0.1361', '-0.0474', '-0.1542', '0.1799', '0.2615', '0.0725', '0.3328', '0.3108', '-0.03488', '0.1831', '-0.2805', '-0.4355', '0.5205', '0.1815', '0.03195', '-0.357', '-0.04272', '0.1268']",,,C567564,,,,
mondo:0013007,combined immunodeficiency due to ORAI1 deficiency,"['IMD9', 'immunodeficiency 9', 'immune dysfunction with T-cell inactivation due to calcium entry defect 1', 'CID due to ORAI1 deficiency', 'immunodeficiency type 9']",0111976,612782,317428,C2748568,"['-0.1438', '0.2058', '0.3218', '-0.5923', '0.2773', '-0.2036', '0.1382', '0.3398', '0.1925', '-0.543', '-0.12256', '0.2678', '-0.844', '-0.0578', '0.3193', '-0.05597', '0.05505', '-0.1108', '-0.3262', '-0.6533', '0.326', '-0.1918', '0.5474', '-0.2717', '-0.3809', '0.1831', '-0.678', '-0.2705', '-0.334', '-0.6494', '-0.4946', '0.5757', '-0.1181', '0.1361', '-0.2742', '-0.3303', '-0.08673', '0.2443', '-0.5737', '-0.1935', '-0.4138', '-0.2316', '0.05167', '-0.3242', '-0.4744', '0.354', '0.04752', '0.3726', '0.4578', '0.452', '-0.2847', '-0.2502', '0.7227', '0.1545', '-0.1322', '-0.3467', '0.471', '-0.3262', '0.2054', '0.3174', '0.4475', '0.4385', '-0.03912', '-0.08655', '0.4353', '-0.12103', '0.2394', '0.3374', '-0.3726', '0.2202', '-0.3926', '-0.03827', '0.3518', '-0.637', '0.1571', '-0.2014', '0.4072', '-0.02026', '-0.02187', '0.3584', '-0.01185', '0.0969', '0.2668', '0.3818', '-0.1407', '0.5845', '0.5493', '0.4084', '0.9014', '0.06232', '0.2046', '0.6597', '0.1813', '0.361', '0.725', '0.917', '0.2554', '-0.12396', '0.1128', '0.1581']",,,C557826,,,,
mondo:0013008,combined immunodeficiency due to STIM1 deficiency,"['STIM1 deficiency', 'immune dysfunction with T-cell inactivation due to calcium entry defect 2', 'CID due to STIM1 deficiency', 'IMD10', 'immunodeficiency type 10', 'immunodeficiency 10']",0111970,612783,317430,C2748557,"['-0.04654', '0.4792', '0.578', '-0.7876', '0.4614', '-0.05905', '0.183', '0.1021', '0.3008', '-0.5176', '-0.2296', '0.03387', '-0.898', '-0.03915', '0.2542', '-0.1771', '-0.3032', '-0.1709', '-0.2837', '-0.7046', '0.06213', '-0.2325', '0.85', '-0.2546', '-0.3867', '0.2008', '-0.4587', '-0.2274', '-0.02747', '-0.4585', '-0.5234', '0.3384', '0.2712', '0.207', '-0.1231', '-0.4473', '-0.3872', '0.1621', '-0.535', '-0.3213', '-0.6973', '-0.2383', '0.1442', '-0.358', '-0.4456', '0.226', '0.4885', '0.406', '0.3547', '-0.058', '-0.2627', '-0.1257', '0.8306', '0.2311', '-0.08954', '-0.2499', '0.3926', '-0.2448', '0.04373', '0.402', '0.3508', '0.1171', '-0.1854', '0.01088', '0.3677', '-0.11743', '0.381', '0.627', '-0.3613', '0.2426', '-0.304', '-0.4258', '0.1644', '-0.3958', '0.133', '-0.33', '0.643', '-0.012634', '0.04776', '0.632', '-0.1769', '0.2269', '0.1832', '0.36', '0.0868', '0.4692', '0.5635', '0.2456', '0.874', '0.05783', '0.4773', '0.6353', '0.2245', '0.1384', '0.8813', '0.797', '0.3098', '-0.05157', '-0.01567', '-0.0501']",,,C557827,,,,
mondo:0013009,Megarbane-Jalkh syndrome,"['developmental delay, dysmorphic features, neonatal spontaneous fractures, wrinkled skin, and hepatic failure', 'developmental delay dysmorphic features neonatal spontaneous fractures wrinkled skin and hepatic failure', 'Megarbane Jalkh syndrome', 'Megarbane-Jalkh syndrome']",,612785,,C2748555,,,,C548071,,,,
mondo:0013010,autosomal recessive nonsyndromic hearing loss 71,"['autosomal recessive deafness 71', 'autosomal recessive nonsyndromic deafness type 71', 'deafness, autosomal recessive 71', 'DFNB71', 'autosomal recessive nonsyndromic deafness 71']",0110522,612789,,C2748554,,,,C567562,,,,
mondo:0013011,atrial septal defect 5,"['atrial heart septal defect type 5', 'atrial heart septal defect caused by mutation in ACTC1', 'atrial septal defect 5', 'ASD5', 'atrial septal defect type 5', 'ACTC1 atrial heart septal defect']",0110110,612794,,C2748552,,,,C567561,,,,
mondo:0013012,inflammatory bowel disease 27,"['IBD27', 'inflammatory bowel disease type 27', 'inflammatory bowel disease 27']",0110902,612796,,C2748550,,,,C567559,,,,
mondo:0013013,"question mark ears, isolated","['Cosman deformity of the auricle', 'QME', 'ears, prominent and constricted', 'question mark ears, isolated', 'question MARK ears, isolated', 'auricular cleft, congenital']",,612798,,,,,,,,,,
mondo:0013014,"spondyloepimetaphyseal dysplasia, aggrecan type","['SEMDAG', 'spondyloepimetaphyseal dysplasia, aggrecan type', 'SEMD, aggrecan type']",,612813,171866,C2748544,"['-0.6714', '0.4126', '0.279', '-0.1577', '0.438', '-0.2788', '-0.1544', '0.561', '-0.3552', '-0.3718', '-0.2832', '0.2883', '0.04028', '0.07605', '0.2659', '0.5464', '0.2544', '0.2036', '-0.10077', '-0.1731', '0.03033', '0.2042', '0.897', '-0.4712', '0.3513', '0.2788', '-0.4075', '-0.384', '0.3972', '-0.26', '0.5376', '-0.073', '0.02744', '0.11383', '0.4487', '-0.2092', '-0.7017', '-0.3982', '-0.3408', '-0.516', '0.1425', '-0.4077', '-0.1394', '-0.1338', '-0.128', '-0.3838', '0.0664', '0.00953', '-0.0783', '-0.6187', '0.352', '-0.10406', '-0.04276', '0.5234', '-0.174', '-1.174', '0.0966', '-0.04044', '0.04053', '0.1633', '0.3706', '-0.03494', '-0.1823', '-0.07587', '-0.21', '0.04987', '0.2156', '0.434', '-0.3533', '0.02625', '-0.2861', '0.1488', '-0.005592', '-0.1786', '-0.4692', '0.5107', '-0.3193', '0.1296', '-0.3027', '-0.02922', '0.1067', '0.0445', '0.111', '0.2942', '-0.343', '0.3804', '0.12067', '0.8574', '0.4973', '0.1538', '-0.5166', '0.332', '-0.011024', '0.10583', '1.002', '0.2231', '0.3284', '-0.621', '0.594', '0.2491']",,,C567558,,,,
mondo:0013015,Brugada syndrome 5,"['Brugada syndrome caused by mutation in SCN1B', 'BRGDA5', 'Brugada syndrome 5', 'Brugada syndrome type 5', 'Cardiac conduction defect, nonspecific', 'SCN1B Brugada syndrome']",0110222,612838,871,C2748541,"['-0.2179', '-0.493', '-0.3848', '0.6846', '0.08405', '-0.2201', '0.152', '0.8', '0.1304', '-0.07416', '0.03546', '-0.4338', '-0.1265', '0.3762', '-0.4045', '0.00579', '-0.781', '-0.409', '-0.2029', '-0.61', '0.6714', '0.682', '0.486', '-0.636', '0.0868', '-0.3018', '0.2036', '0.4229', '0.386', '-0.1401', '0.6504', '0.401', '0.4175', '0.2205', '-0.3232', '-0.9585', '0.379', '-0.4282', '0.05396', '0.0638', '0.3428', '-0.0362', '0.72', '-0.3364', '-0.3367', '0.1614', '-1.163', '-0.1849', '-0.5034', '0.4827', '0.2673', '0.3347', '0.2295', '-0.10645', '0.547', '-0.486', '0.4668', '0.06076', '-0.4053', '-0.3877', '-0.224', '0.3623', '0.7705', '-0.08374', '-0.3284', '0.4788', '0.8315', '1.059', '-0.1587', '-0.491', '-0.04245', '0.258', '0.194', '-0.0711', '0.6353', '0.4731', '-0.1081', '0.1475', '-0.4365', '-0.469', '-0.2637', '0.2537', '0.297', '0.1301', '0.4675', '0.2186', '0.6904', '-0.2031', '-0.105', '-0.2727', '0.3862', '0.0685', '0.04984', '0.3606', '0.8584', '0.6206', '0.9077', '-0.679', '-0.5254', '0.3867']",,,,,,,
mondo:0013016,leukocyte adhesion deficiency 3,"['leukocyte adhesion deficiency 1 variant', 'leukocyte adhesion deficiency caused by mutation in FERMT3', 'integrin activation deficiency disease', 'lad-1 variant', 'leukocyte adhesion deficiency, type 3', 'leukocyte adhesion deficiency type 3', 'LAD1 variant', 'leukocyte adhesion deficiency, type III', 'LAD3', 'IADD', 'lad-III', 'FERMT3 leukocyte adhesion deficiency', 'leukocyte adhesion deficiency 3', 'leukocyte adhesion deficiency-1 variant', 'LAD1V', 'integrin Activation deficiency disease', 'leukocyte adhesion deficiency type III']",0110912,612840,99844,C2748536,"['0.01224', '-0.04483', '-0.2047', '-0.1821', '-0.06082', '-0.5044', '0.06024', '0.1687', '0.1292', '0.10394', '-0.4727', '-0.1448', '0.122', '0.1722', '-0.3677', '0.03134', '-0.05994', '-0.0651', '-0.262', '-0.5786', '-0.743', '-0.2482', '0.8013', '0.07544', '-0.1903', '0.03433', '-0.1857', '0.057', '0.2285', '-0.4832', '-0.309', '0.629', '0.52', '0.02347', '0.05856', '0.0381', '-0.3079', '-0.4731', '-0.01074', '-0.05176', '-0.1777', '-0.2625', '0.012634', '-0.4102', '-0.1392', '0.1696', '-0.5337', '0.09033', '-0.1514', '-0.3887', '0.3884', '-0.4768', '0.604', '0.1122', '-0.2964', '0.05176', '0.1881', '0.1931', '-0.262', '0.2202', '-0.2365', '0.3552', '0.2927', '-0.2238', '0.397', '0.1514', '0.2106', '0.06116', '-0.4968', '0.4177', '-0.0914', '-0.4858', '-0.316', '-0.3735', '0.838', '0.2056', '0.2007', '-0.01695', '0.2279', '0.1453', '-0.4243', '-0.1061', '-0.4268', '0.3018', '0.1509', '-0.167', '0.348', '0.398', '0.7075', '0.0572', '0.1836', '0.389', '0.1687', '-0.04654', '0.646', '1.141', '0.1403', '-0.5957', '0.6377', '0.10443']",,,C567555,,,,
mondo:0013017,hypotrichosis 5,"['hypotrichosis 5', 'HYPT5', 'Muhh2', 'hypt5', 'hypotrichosis type 5', 'Marie Unna hereditary hypotrichosis 2']",0110702,612841,,C2748535,,,,C567554,,,,
mondo:0013018,"keratosis follicularis spinulosa decalvans, autosomal dominant","['keratosis follicularis SPINULOSA decalvans, autosomal dominant', 'keratosis follicularis spinulosa decalvans, autosomal dominant', 'KFSD']",0080755,612843,,C2748527,,,,C567553,,,,
mondo:0013020,"narcolepsy 5, susceptibility to","['NRCLP5', 'narcolepsy 5, susceptibility to', 'narcolepsy 5']",,612851,,C2748508,,,,,,,,
mondo:0013021,sterile multifocal osteomyelitis with periostitis and pustulosis,"['autoinflammatory disease due to interleukin-1 receptor antagonist deficiency', 'osteomyelitis, STERILE multifocal, with periostitis and pustulosis', 'Interleukin-1 receptor antagonist deficiency', 'deficiency of interleukin-1 receptor antagonist', 'deficiency of the Interleukin-1 receptor antagonist', 'DIRA', 'Interleukin 1 receptor antagonist deficiency', 'OMPP']",,612852,210115,C2748507,"['0.0591', '-0.1273', '-0.445', '0.1117', '-0.2042', '-0.03485', '-0.4282', '0.073', '-0.468', '-0.441', '-0.2013', '0.3333', '0.04535', '0.2844', '-0.607', '0.0003183', '-0.277', '0.1792', '-0.4446', '-0.568', '0.2708', '-0.02002', '0.0264', '-0.2898', '-0.04056', '-0.2072', '-0.278', '-0.009384', '-0.2083', '0.2258', '0.1371', '-0.07227', '0.01317', '-0.3604', '0.498', '0.515', '-0.6187', '-0.1036', '0.09375', '-0.5996', '-0.4895', '-0.5522', '0.2361', '-0.2725', '0.1344', '0.3086', '-0.5767', '-0.548', '0.10254', '0.2383', '-0.0379', '-0.2683', '0.3442', '0.138', '-0.2612', '-0.3083', '-0.4644', '0.3242', '-0.5684', '-0.02008', '0.2454', '0.2512', '-0.992', '0.2764', '0.1049', '0.4417', '0.1334', '0.6704', '-0.505', '0.8345', '0.05524', '0.177', '-0.1805', '-0.43', '-0.3071', '0.1074', '-0.04828', '0.4429', '0.4912', '-0.04034', '-0.7866', '0.1029', '0.2357', '0.5737', '-0.4167', '0.1458', '0.0509', '0.1652', '-0.0739', '0.248', '0.2345', '0.1898', '-0.1833', '0.3142', '0.1914', '0.427', '0.5503', '-0.8745', '-0.006554', '-0.2556']",C119056,,C557815,,,,
mondo:0013022,"restless legs syndrome, susceptibility to, 7","['restless legs syndrome 7', 'restless legs syndrome, susceptibility to, 7', 'RLS7']",,612853,,,,,,,,,,
mondo:0013023,orofacial cleft 12,"['OFC12', 'cleft lip with or without cleft palate, nonsyndromic, 12', 'orofacial cleft 12']",0080405,612858,,C2748505,,,,C567548,,,,
mondo:0013024,chronic thromboembolic pulmonary hypertension,"['Cteph, Dvt-negative, susceptibility to', 'CTEPH', 'pulmonary hypertension, chronic thromboembolic, without deep vein thrombosis, susceptibility to']",,612862,70591,C2363973,,,,,416.8,,10068739,
mondo:0013025,chromosome 6q24-q25 deletion syndrome,"['del(6q25)', 'monosomy 6q25', 'deletion 6q25', '6q25 microdeletion syndrome', 'chromosome 6q25 microdeletion syndrome', 'chromosome 6q24-q25 deletion syndrome', 'chromosome 6q25-q25 deletion syndrome', 'Del(6)(q25)']",0060424,612863,251056,C4304527,,C36470,,,,,,
mondo:0013026,subepithelial mucinous corneal dystrophy,"['corneal dystrophy, subepithelial mucinous', 'subepithelial mucinous corneal dystrophy', 'SMCD']",0060454,612867,98959,C2748503,,,,C567547,,,,
mondo:0013027,posterior amorphous corneal dystrophy,"['PACD', 'posterior amorphous stromal dystrophy', 'corneal dystrophy, POSTERIOR amorphous', 'chromosome 12Q21.33 deletion syndrome', 'posterior amorphous corneal dystrophy']",0060452,612868,98971,C2748502,,,,C567546,,,,
mondo:0013028,adenosine monophosphate deaminase deficiency,"['AMP deaminase deficiency', 'myoadenylate deaminase deficiency']",,,45,,"['-0.964', '-0.04282', '-0.2502', '-0.1573', '0.2598', '-0.9053', '-0.1648', '0.8286', '-0.468', '-0.2886', '-0.03406', '-0.1781', '-0.1029', '0.4634', '0.2091', '0.2446', '0.1465', '-0.1448', '-0.9507', '-0.502', '-0.01787', '-0.622', '0.8535', '-0.4258', '-0.10425', '-0.132', '0.7773', '-0.3167', '-0.4695', '-0.2446', '0.2305', '-0.2484', '0.0356', '0.1322', '-0.4077', '0.1254', '0.04932', '0.04636', '0.01941', '0.3076', '0.4102', '-0.3774', '-0.07935', '-0.4602', '0.448', '0.1028', '0.014435', '0.0186', '-0.1362', '0.62', '0.2793', '-0.2047', '0.4353', '-0.008675', '0.6567', '-0.2856', '0.5796', '-0.2725', '-0.2734', '0.6064', '0.04233', '0.11865', '0.4653', '-0.823', '-0.5063', '0.1019', '0.0636', '0.4895', '-0.4949', '-0.3816', '0.02182', '-0.1882', '-0.5713', '0.06494', '1.057', '0.4055', '-0.003433', '-0.0955', '-0.02058', '0.2556', '0.266', '-0.3962', '0.4797', '0.08685', '0.0627', '0.3384', '-0.131', '-0.0624', '0.422', '-0.03802', '0.3616', '-0.1816', '-0.2466', '-0.1897', '0.75', '0.1934', '-0.3838', '-0.759', '-0.1947', '-0.2854']",,,C538234,277.2,,,
mondo:0013029,cerebellar ataxia type 9,"['cerebellar ataxia type 9', 'SCA9', 'spinocerebellar ataxia 9', 'spinocerebellar ataxia type 9']",0111747,612876,,C3887996,,,,,,,,
mondo:0013030,dilated cardiomyopathy 1BB,"['cardiomyopathy, dilated, type 1Bb', 'CMD1BB', 'cardiomyopathy, dilated, 1BB', 'dilated cardiomyopathy type 1BB', 'familial isolated dilated cardiomyopathy caused by mutation in DSG2', 'DSG2 familial isolated dilated cardiomyopathy']",0110458,612877,,C2752072,,,,C567877,,,,
mondo:0013031,"chromosome 5Q14.3 deletion syndrome, distal","['periventricular nodular heterotopia 5', 'heterotopia, periventricular, associated with chromosome 5Q deletion', 'chromosome 5Q14.3 deletion syndrome, distal']",,612881,,C2752071,,,,C567876,,,,
mondo:0013032,"epilepsy, idiopathic generalized, susceptibility to, 8","['susceptibility to idiopathic generalised epilepsy 8', 'epilepsy idiopathic generalized, susceptibility to, 8', 'susceptibility to idiopathic generalized epilepsy 8', 'epilepsy, idiopathic generalized, susceptibility to, type 8', 'CASR generalised epilepsy', 'generalized epilepsy caused by mutation in CASR', 'epilepsy, idiopathic generalized, susceptibility to, 8', 'EIG8', 'generalised epilepsy caused by mutation in CASR', 'CASR generalized epilepsy']",0111322,612899,,,,,,,,,,
mondo:0013033,"cerebral palsy, spastic quadriplegic, 2","['spastic quadriplegia caused by mutation in KANK1', 'cerebral palsy, spastic quadriplegic, type 2', 'KANK1 spastic quadriplegia', 'CPSQ2', 'cerebral palsy, spastic quadriplegic, 2']",0081360,612900,,C2752061,,,,C567867,,,,
mondo:0013034,keratosis palmoplantaris striata 2,"['PPKS2', 'DSP striate palmoplantar keratoderma', 'keratosis palmoplantaris striata II', 'keratoderma, palmoplantar, striate form 2', 'striate palmoplantar keratoderma 2', 'keratosis palmoplantaris striata type 2', 'striate palmoplantar keratoderma caused by mutation in DSP']",0081109,612908,,C1852127,,,,C565102,,,,
mondo:0013035,orofaciodigital syndrome XI,"['orofaciodigital syndrome type XI', 'oral-facial-digital syndrome type 11', 'oral facial digital syndrome 11', 'orofaciodigital syndrome 11', 'OFD11', 'oral facial digital syndrome type 11', 'oral-facial-digital syndrome, Gabrielli type', 'Gabrielli syndrome', 'Ofds 11', 'oral-Facial-digital syndrome with skeletal anomalies', 'oral-Facial-digital syndrome, type 11', 'orofaciodigital syndrome XI', 'orofaciodigital syndrome type 11', 'OFD syndrome 11', 'orofaciodigital syndrome, Gabrielli type']",0060381,612913,141000,,,,,C557821,,,,
mondo:0013036,Zechi-Ceide syndrome,"['occipital atretic cephalocele, unusual facies, and large feet', 'occipital atretic cephalocele, unusual facies and large feet', 'Zechi Ceide syndrome', 'occipital atretic cephalocele-unusual facies-large feet syndrome', 'Zechi-Ceide syndrome']",,612916,217017,C2752047,,,,C567865,,,,
mondo:0013037,Giacheti syndrome,"['Giacheti syndrome', 'Marfanoid habitus and specific language and learning disabilities']",,612917,,C2752043,,,,C567864,,,,
mondo:0013038,CLOVES syndrome,"['congenital lipomatous overgrowth-vascular malformation-epidermal nevi-spinal anomaly syndrome', 'congenital lipomatous overgrowth, vascular malformations, and EPIDERMAL nevi', 'CLOVE syndrome, somatic', 'congenital lipomatous overgrowth - vascular malformation - epidermal nevi', 'CLOVE syndrome', 'congenital lipomatous overgrowth-vascular malformation-epidermal nevi-skeletal anomaly syndrome', 'CLOVES syndrome', 'congenital lipomatous overgrowth, vascular malformations, Epidermal nevi, and skeletal/spinal abnormalities', 'congenital lipomatous overgrowth, vascular malformations, and epidermal nevi']",0080351,612918,140944,C2752042,"['-0.1927', '0.508', '-0.1697', '-0.7085', '0.2426', '-0.1357', '-0.04977', '-0.058', '-0.1476', '-0.4175', '-0.156', '-0.3867', '0.05872', '-0.239', '0.1908', '-0.2805', '0.1572', '-0.2651', '-0.7446', '-0.53', '0.283', '0.04562', '0.676', '-0.575', '-0.1211', '0.3323', '-0.1582', '-0.0879', '0.347', '0.4473', '0.514', '-0.2324', '0.488', '0.5117', '0.1381', '-0.161', '-0.101', '-0.2278', '-0.284', '0.2289', '0.2434', '-0.742', '0.3623', '0.1565', '0.267', '-0.4092', '-0.11005', '-0.2115', '-0.3403', '-0.3713', '0.139', '0.04916', '0.0589', '0.3086', '-0.6562', '-0.1256', '0.0776', '-0.3455', '-0.06104', '0.11096', '0.5303', '-0.452', '-0.01709', '0.2001', '-0.351', '0.0743', '0.4785', '0.5884', '-0.9453', '0.606', '-0.0912', '0.0553', '0.02133', '-0.4397', '-0.4573', '-0.1476', '-0.2261', '0.3413', '-0.332', '-0.6475', '0.3218', '0.218', '-0.04047', '0.8706', '-0.2642', '0.003546', '-0.1603', '0.3813', '-0.268', '-0.2062', '0.3262', '0.2482', '-0.0909', '0.606', '0.693', '-0.4856', '0.773', '-0.2186', '0.3525', '0.03452']",,,C567863,,,,
mondo:0013039,3M syndrome 2,"['three M syndrome type 2', '3M syndrome 2', 'three M syndrome 2', '3M2', 'OBSL1 3-M syndrome', '3-M syndrome caused by mutation in OBSL1', '3-M syndrome 2']",,612921,,C2752041,,,,C567862,,,,
mondo:0013040,atypical hemolytic-uremic syndrome with MCP/CD46 anomaly,"['hemolytic uremic syndrome, atypical, susceptibility to, type 2', 'aHUS2', 'aHUS with MCP/CD46 anomaly', 'atypical HUS with MCP/CD46 anomaly', 'hemolytic-uremic syndrome without diarrhea with MCP/CD46 anomaly', 'AHUS, susceptibility to, 2', 'AHUS2', 'susceptibility to atypical hemolytic uremic syndrome 2', 'D-HUS with MCP/CD46 anomaly', 'hemolytic uremic syndrome, atypical, susceptibility to, 2', 'hemolytic-uremic syndrome without diarrhoea with MCP/CD46 anomaly']",,612922,93576,,"['-0.09235', '0.11835', '0.02571', '-0.02496', '0.06128', '-0.0924', '-0.00964', '0.08374', '-0.0439', '-0.02184', '-0.002172', '-0.03217', '0.047', '0.006737', '-0.0684', '-0.08246', '-0.0461', '-0.0653', '0.00485', '-0.2075', '0.01187', '-0.01563', '0.1078', '-0.0474', '0.0841', '0.02168', '-0.0587', '-0.0651', '0.03076', '-0.05185', '0.11694', '0.043', '0.1626', '0.0989', '0.03745', '-0.06714', '-0.02965', '-0.04272', '-0.02382', '-0.12225', '0.04892', '-0.1117', '0.03366', '-0.08136', '0.037', '-0.11804', '-0.05762', '0.07874', '-0.0128', '0.0232', '-0.01441', '-0.0098', '-0.0203', '-0.006283', '-0.1061', '-0.0686', '0.0923', '-0.06384', '-0.1683', '0.0387', '0.07794', '0.03992', '0.013756', '0.00361', '0.04117', '0.014244', '0.1735', '0.0465', '-0.1071', '0.1404', '-0.1231', '0.007095', '0.034', '-0.05313', '0.06204', '0.03845', '0.01522', '-0.02438', '-0.06027', '-0.04486', '0.009315', '0.05334', '-0.04446', '0.08234', '-0.05652', '-0.07825', '0.0733', '0.09845', '0.102', '0.004356', '0.1099', '0.11346', '0.02943', '0.0216', '0.2198', '0.05582', '0.1372', '-0.1923', '-0.02568', '0.04703']",,,,,,,
mondo:0013041,atypical hemolytic-uremic syndrome with I factor anomaly,"['D-HUS with I factor anomaly', 'hemolytic-uremic syndrome without diarrhea with I factor anomaly', 'hemolytic uremic syndrome, atypical, susceptibility to, type 3', 'aHUS, susceptibility to, 3', 'AHUS3', 'hemolytic uremic syndrome, atypical, susceptibility to, 3', 'aHUS with I factor anomaly', 'aHUS3', 'hemolytic-uremic syndrome without diarrhoea with I factor anomaly', 'atypical HUS with I factor anomaly', 'susceptibility to atypical hemolytic uremic syndrome 3']",,612923,93580,,"['-0.1008', '0.1251', '0.02905', '-0.03317', '0.0765', '-0.0796', '-0.00863', '0.0819', '-0.05966', '-0.02696', '-0.02982', '-0.02246', '0.0988', '-0.01246', '-0.1219', '-0.1225', '-0.002604', '-0.0737', '-0.02695', '-0.2622', '0.01111', '-0.06207', '0.2179', '-0.02658', '0.11926', '0.0643', '-0.0417', '-0.0683', '0.01191', '-0.07825', '0.12366', '0.04272', '0.192', '0.09454', '-0.02057', '-0.1378', '-0.02034', '-0.05154', '-0.05432', '-0.203', '0.03056', '-0.1361', '0.04114', '-0.06046', '0.04593', '-0.1616', '-0.01712', '0.11914', '-0.01151', '0.05026', '-0.02615', '-0.0799', '-0.0726', '-0.04108', '-0.1438', '-0.0547', '0.1208', '-0.12317', '-0.2156', '0.07605', '0.0708', '0.05447', '0.04944', '0.038', '0.03001', '0.04572', '0.1791', '0.063', '-0.1642', '0.1771', '-0.1642', '-0.002094', '0.0582', '-0.06305', '0.09247', '0.04773', '-0.015205', '-0.0336', '-0.0645', '-0.02765', '0.001238', '0.0444', '-0.05997', '0.10596', '-0.0679', '-0.06494', '0.0635', '0.1908', '0.1606', '-0.0505', '0.08936', '0.1658', '0.04593', '0.03552', '0.293', '0.0933', '0.1222', '-0.2139', '-0.01157', '0.071']",,,,,,,
mondo:0013042,atypical hemolytic-uremic syndrome with B factor anomaly,"['hemolytic uremic syndrome, atypical, susceptibility to, 4', 'susceptibility to atypical hemolytic uremic syndrome 4', 'aHUS4', 'AHUS4', 'D-HUS with B factor anomaly', 'aHUS with B factor anomaly', 'aHUS, susceptibility to, 4', 'hemolytic-uremic syndrome without diarrhea with B factor anomaly', 'hemolytic-uremic syndrome without diarrhoea with B factor anomaly', 'atypical HUS with B factor anomaly', 'hemolytic uremic syndrome, atypical, susceptibility to, type 4']",,612924,93578,,"['-0.0778', '0.1278', '0.02974', '-0.04626', '0.07385', '-0.09686', '-0.0265', '0.0566', '-0.02908', '-0.041', '-0.02127', '0.004986', '0.0454', '0.0056', '-0.1285', '-0.1372', '-0.02394', '-0.04764', '-0.0497', '-0.2446', '0.02501', '-0.1057', '0.1632', '-0.04538', '0.1065', '-0.002743', '-0.03378', '-0.05136', '0.005344', '-0.08545', '0.1562', '0.06155', '0.2037', '0.1233', '0.02806', '-0.08655', '-0.0514', '-0.055', '-0.07556', '-0.1813', '0.02594', '-0.1506', '0.0228', '-0.11115', '0.02158', '-0.1442', '-0.06055', '0.09894', '0.007286', '0.05542', '0.02084', '-0.0692', '-0.0387', '-0.004242', '-0.1753', '-0.022', '0.11426', '-0.11505', '-0.2218', '0.04083', '0.05844', '0.0399', '0.0763', '0.02203', '0.0793', '0.06033', '0.1985', '0.04703', '-0.1603', '0.1705', '-0.1893', '-0.01457', '0.0566', '-0.05063', '0.11334', '-0.0008926', '0.00584', '-0.03137', '-0.08167', '-0.0428', '-0.03668', '0.0302', '-0.03613', '0.10406', '-0.08905', '-0.0854', '0.07983', '0.1437', '0.1676', '-0.05804', '0.1384', '0.1486', '0.04135', '0.0273', '0.221', '0.096', '0.09796', '-0.277', '-0.02893', '0.03452']",,,,,,,
mondo:0013043,atypical hemolytic-uremic syndrome with C3 anomaly,"['susceptibility to atypical hemolytic uremic syndrome 5', 'hemolytic-uremic syndrome without diarrhoea with C3 anomaly', 'hemolytic uremic syndrome, atypical, susceptibility to, 5', 'hemolytic uremic syndrome, atypical, susceptibility to, type 5', 'AHUS5', 'D-HUS with C3 anomaly', 'aHUS with C3 anomaly', 'atypical HUS with C3 anomaly', 'Ahus, susceptibility to, 5', 'hemolytic-uremic syndrome without diarrhea with C3 anomaly']",,612925,93575,,"['-0.11365', '0.12445', '0.01843', '-0.04077', '0.04733', '-0.0726', '-0.008224', '0.04916', '-0.04968', '0.01014', '-0.04193', '-0.01315', '0.03952', '0.01823', '-0.0885', '-0.0901', '-0.05002', '-0.0726', '-0.02194', '-0.2169', '0.03375', '-0.0444', '0.1605', '-0.05225', '0.1019', '0.019', '-0.05087', '-0.04813', '-0.005043', '-0.04752', '0.1155', '0.02463', '0.167', '0.11975', '0.03577', '-0.0923', '0.007587', '0.01104', '-0.0326', '-0.1453', '0.015015', '-0.1039', '0.01747', '-0.09064', '0.03528', '-0.1392', '-0.0407', '0.0759', '0.002195', '0.0691', '-0.00906', '-0.03598', '-0.0174', '-0.02289', '-0.1498', '-0.04343', '0.09674', '-0.11145', '-0.1765', '0.0672', '0.05685', '0.0657', '0.01804', '0.00691', '0.05203', '0.0293', '0.1813', '0.04282', '-0.11145', '0.1495', '-0.1555', '0.02994', '0.05472', '-0.06805', '0.0588', '0.0419', '-0.002245', '-0.001604', '-0.0699', '-0.05206', '-0.00394', '0.03043', '-0.03522', '0.10504', '-0.05783', '-0.0647', '0.03445', '0.09485', '0.1302', '-0.04095', '0.1365', '0.1268', '0.04053', '0.0186', '0.2252', '0.1004', '0.1073', '-0.2451', '-0.0664', '0.06885']",,,,,,,
mondo:0013044,atypical hemolytic-uremic syndrome with thrombomodulin anomaly,"['atypical HUS with thrombomodulin anomaly', 'Ahus, susceptibility to, 6', 'hemolytic-uremic syndrome without diarrhea with thrombomodulin anomaly', 'aHUS with thrombomodulin anomaly', 'hemolytic-uremic syndrome without diarrhoea with thrombomodulin anomaly', 'AHUS6', 'D-HUS with thrombomodulin anomaly', 'hemolytic uremic syndrome, atypical, susceptibility to, 6', 'susceptibility to atypical hemolytic uremic syndrome 6', 'hemolytic uremic syndrome, atypical, susceptibility to, type 6']",,612926,217023,,"['-0.0864', '0.10614', '0.014145', '-0.01949', '0.05548', '-0.1184', '-0.02495', '0.1115', '-0.0639', '0.005775', '-0.02933', '-0.00584', '0.04477', '0.00968', '-0.07605', '-0.0898', '-0.0358', '-0.07983', '0.001538', '-0.2086', '0.01959', '-0.03256', '0.1328', '-0.04852', '0.0869', '0.01335', '-0.0586', '-0.07666', '0.02296', '-0.05637', '0.1062', '0.00501', '0.1581', '0.12146', '0.02585', '-0.06143', '-0.02153', '-0.03995', '-0.04535', '-0.12463', '0.0267', '-0.11127', '0.04047', '-0.09357', '0.02055', '-0.0876', '-0.08856', '0.0964', '-0.02182', '0.0623', '0.000849', '-0.01566', '-0.0395', '-0.0237', '-0.1149', '-0.06836', '0.1089', '-0.0819', '-0.1746', '0.04016', '0.08746', '0.04388', '0.01325', '0.014565', '0.02373', '0.00833', '0.1841', '0.06506', '-0.11633', '0.1597', '-0.1251', '0.00965', '0.07336', '-0.05185', '0.0722', '0.0376', '-0.001751', '-0.0418', '-0.082', '-0.04208', '0.014404', '0.03745', '-0.0233', '0.1153', '-0.0401', '-0.05655', '0.04266', '0.121', '0.1164', '0.002584', '0.1433', '0.1125', '0.02756', '0.03674', '0.2422', '0.05362', '0.1273', '-0.1964', '-0.0251', '0.05066']",,,,,,,
mondo:0013045,"mycobacterium tuberculosis, susceptibility to, 3","['MTBS3', 'Mycobacterium tuberculosis, susceptibility to, type 3', 'mycobacterium tuberculosis, susceptibility to, 3']",,612929,,,,,,,,,,
mondo:0013046,glycogen storage disease due to muscle beta-enolase deficiency,"['glycogen storage disease XIII', 'glycogenosis due to muscle beta-enolase deficiency', 'GSDXIII', 'GSD13', 'glycogenosis type 13', 'glycogen storage disease 13', 'muscular enolase deficiency', 'GSD due to muscle beta-enolase deficiency', 'GSD 13', 'enolase 3 deficiency', 'muscle enolase deficiency', 'glycogen storage disease type 13', 'enolase-Beta deficiency']",,612932,99849,C2752027,"['-0.556', '-0.00689', '-0.10114', '0.2279', '0.3716', '-0.41', '-0.2747', '0.4243', '-0.0574', '0.1025', '0.07367', '-0.023', '-0.04532', '0.001464', '-0.1277', '-0.01384', '-0.1631', '-0.1311', '-0.7173', '-0.5576', '0.3162', '-0.1765', '0.4492', '-0.1052', '-0.1943', '-0.387', '0.083', '-0.2479', '-0.1213', '-0.181', '0.153', '0.1262', '0.2076', '0.178', '-0.2236', '-0.3452', '-0.23', '0.1841', '-0.04843', '-0.2812', '0.2065', '-0.2192', '0.00537', '0.09296', '-0.3242', '-0.005127', '-0.04465', '0.208', '-0.05118', '0.4036', '0.0001655', '-0.4104', '0.518', '0.00708', '-0.1508', '-0.6733', '0.488', '0.11285', '-0.4155', '-0.02386', '0.1526', '-0.0426', '0.4092', '-0.1954', '-0.4817', '0.216', '0.2119', '0.1809', '-0.52', '-0.2416', '-0.2573', '0.02106', '0.04703', '0.1257', '0.1566', '0.2412', '0.2423', '0.2097', '-0.3806', '0.1261', '-0.2098', '0.05618', '0.1316', '0.04282', '0.3218', '0.2235', '0.4187', '0.1993', '0.3354', '0.0427', '0.1538', '0.2874', '-0.1003', '-0.1392', '0.727', '0.3564', '0.1666', '-0.3062', '-0.1203', '0.2234']",,,C567861,,,,
mondo:0013047,glycogen storage disease due to lactate dehydrogenase M-subunit deficiency,"['GSD 11', 'glycogen storage disease type 11', 'glycogenosis due to lactate dehydrogenase M-subunit deficiency', 'lactate dehydrogenase deficiency type A', 'LDHA glycogen storage disease', 'GSD type 11', 'GSD11', 'GSD XI', 'glycogen storage disease caused by mutation in LDHA', 'LDH-M subunit deficiency', 'glycogenosis type 11', 'GSD due to lactate dehydrogenase M-subunit deficiency', 'glycogen storage disease XI', 'lactate dehydrogenase A deficiency']",,612933,284426,,"['-0.06384', '0.3462', '-0.4175', '-0.1174', '0.0374', '-0.4458', '-0.3123', '-0.05493', '-0.1558', '0.1003', '0.05872', '0.3755', '0.08527', '0.2013', '-0.5957', '0.1805', '-0.1729', '-0.05035', '-0.57', '-0.2869', '0.4797', '-0.147', '0.348', '0.1012', '-0.4854', '0.03473', '0.1755', '0.2319', '-0.1682', '0.3613', '0.531', '-0.416', '0.3667', '-0.0983', '0.02063', '-0.1566', '-0.2375', '0.1655', '0.04193', '0.045', '-0.158', '-0.4707', '-0.2263', '0.479', '-0.4766', '-0.05377', '0.1559', '0.1439', '0.248', '0.607', '-0.0254', '-0.04135', '0.4944', '0.1158', '0.2705', '-0.3457', '0.2686', '0.08234', '-0.3818', '-0.258', '0.607', '0.08777', '-0.05838', '-0.3474', '-0.5283', '0.1598', '0.1015', '0.2412', '-0.2386', '0.1863', '-0.2744', '-0.2996', '0.1758', '0.1775', '0.312', '0.5254', '0.2744', '0.712', '0.1655', '-0.0807', '-0.01536', '-0.3801', '0.411', '-0.1086', '-0.0717', '0.28', '-0.1671', '0.06683', '0.7607', '0.08325', '0.7026', '-0.097', '-0.02492', '0.12354', '0.8677', '0.6533', '0.0444', '0.06366', '-0.0747', '0.09296']",,,C538133,271.8,,,
mondo:0013048,hereditary spastic paraplegia 50,"['cerebral palsy, spastic quadriplegic, 3', 'hereditary spastic paraplegia type 50', 'AP4M1 hereditary spastic paraplegia', 'hereditary spastic paraplegia caused by mutation in AP4M1', 'cerebral palsy, spastic quadriplegic, 3, formerly', 'spastic paraplegia 50, autosomal recessive', 'SPG50', 'autosomal recessive spastic paraplegia 50']",0110802,612936,,C2752008,,,,C567858,,,,
mondo:0013049,DPM3-congenital disorder of glycosylation,"['DPM3-CDG', 'congenital disorder of glycosylation type 1o', 'carbohydrate deficient glycoprotein syndrome type Io', 'congenital disorder of glycosylation type Io', 'Cdg1(Dpm3)', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 15', 'CDG Io', 'congenital disorder of glycosylation, type Io', 'CDGIo', 'CDG-Io', 'CDG1O', 'DG1O', 'DPM3-CDG (CDG-Io)', 'CDG syndrome type Io']",,612937,263494,C2752007,"['-0.7666', '-0.0181', '0.0741', '-0.00994', '0.3643', '-0.7188', '-0.4753', '0.4094', '-0.3838', '-0.0747', '-0.03668', '0.08545', '0.1499', '-0.4968', '-0.05652', '-0.01461', '-0.1562', '-0.2668', '-0.1526', '-0.927', '0.2413', '0.2026', '0.1733', '-0.2142', '0.01738', '0.2515', '0.1569', '0.11194', '0.219', '-0.502', '0.0907', '0.389', '0.3743', '-0.1819', '-0.6636', '-0.4248', '-0.261', '-0.1757', '-0.09125', '-0.2583', '0.168', '-0.621', '0.02899', '-0.08026', '0.2617', '0.4995', '-0.1743', '0.4277', '0.2031', '0.0682', '-0.3127', '0.0851', '-0.1669', '0.2686', '-0.12427', '-0.892', '0.4941', '-0.074', '-0.549', '0.0446', '0.3157', '-0.001437', '0.2268', '-0.2664', '-0.3945', '-0.0366', '0.3174', '0.3743', '-0.863', '-0.1906', '-0.506', '0.05786', '0.1791', '0.0842', '0.3489', '0.195', '-0.11993', '0.1459', '-0.10254', '0.1062', '0.5825', '0.006493', '-0.1836', '0.2461', '0.3447', '0.1703', '0.11127', '0.2128', '0.4404', '-0.2499', '-0.1705', '0.387', '0.2195', '0.2198', '0.8877', '0.2993', '0.571', '-0.2225', '-0.08057', '-0.10175']",,,C567857,,,,
mondo:0013050,"lethal polymalformative syndrome, Boissel type","['GDFD', 'growth retardation, developmental delay, facial dysmorphism', 'growth retardation, developmental delay, and facial dysmorphism']",,612938,210144,,"['-0.02509', '0.08875', '0.5034', '-0.2976', '-0.0769', '-0.2988', '0.07263', '0.4062', '-0.5195', '-0.0673', '-0.1919', '-0.2446', '-0.05127', '-0.219', '-0.436', '-0.05887', '0.2015', '-0.06445', '-0.1095', '-0.511', '-0.05017', '-0.02946', '0.3572', '-0.2372', '0.2004', '-0.1992', '-0.255', '-0.1233', '0.5713', '-0.284', '0.1815', '0.0862', '0.578', '0.1761', '0.1937', '-0.0901', '-0.3235', '-0.255', '-0.2289', '-0.3052', '0.06616', '-0.3535', '-0.026', '0.00848', '-0.0387', '-0.1976', '-0.05725', '0.4438', '-0.051', '-0.003345', '-0.1398', '0.02786', '-0.03473', '-0.1975', '-0.4326', '-0.2798', '-0.3062', '-0.0456', '-0.01177', '0.1221', '-0.0321', '0.1361', '-0.3848', '0.04382', '-0.1586', '-0.1755', '0.2463', '0.1511', '-0.3445', '0.3894', '-0.455', '0.3186', '0.1246', '-0.03723', '-0.3218', '-0.2074', '0.2603', '-0.3723', '-0.2451', '-0.0607', '0.1813', '0.12476', '-0.2073', '0.516', '-0.00676', '0.010544', '0.079', '0.4993', '0.2032', '0.03894', '0.1685', '0.4915', '0.322', '0.1676', '0.4214', '0.2852', '0.4937', '-0.2435', '0.425', '0.245']",,,C567856,,,,
mondo:0013051,autosomal recessive cutis laxa type 2B,"['autosomal recessive cutis laxa type 2 caused by mutation in PYCR1', 'ARCL2B', 'cutis laxa with progeroid features', 'PYCR1 autosomal recessive cutis laxa type 2', 'autosomal recessive cutis laxa type IIB', 'ARCL2, progeroid type', 'autosomal recessive cutis laxa type 2, progeroid type', 'cutis laxa, autosomal recessive, type IIB', 'cutis laxa, autosomal recessive, type 2B', 'cutis laxa, autosomal recessive type 2B']",0070137,612940,357064,C2751987,"['-0.3474', '-0.08044', '0.2905', '-0.4932', '0.4204', '-0.7085', '-0.3628', '0.539', '-0.4685', '-0.1503', '-0.6445', '-0.0966', '0.1925', '0.2886', '-0.2366', '0.3442', '0.5054', '0.03705', '-0.1758', '-0.699', '-0.003813', '-0.2114', '0.1732', '0.3071', '0.0468', '0.1777', '-0.1918', '0.01016', '0.4329', '-0.2063', '0.1958', '-0.2262', '0.4756', '0.6377', '-0.05286', '-0.3103', '-0.1875', '-0.0777', '-0.1981', '0.01599', '-0.07526', '-0.502', '-0.1792', '0.488', '0.1055', '-0.2268', '0.207', '0.4895', '0.05676', '-0.3176', '-0.1411', '-0.02385', '0.4866', '0.11395', '-0.7876', '-0.2817', '-0.07275', '0.2898', '-0.3232', '-0.1522', '0.3762', '-0.3384', '-0.4565', '0.04224', '0.2115', '-0.0392', '0.0787', '0.549', '-0.1835', '0.06384', '-0.3406', '-0.04065', '-0.12213', '-0.01333', '0.2153', '0.10455', '-0.084', '-0.146', '-0.0956', '-0.1208', '-0.2437', '-0.1704', '-0.4238', '0.4902', '-0.2664', '0.3755', '0.138', '0.546', '0.004383', '0.1393', '0.4263', '0.503', '0.1683', '0.04758', '0.386', '0.2756', '0.671', '-0.401', '0.4075', '0.2074']",,,C567855,,,,
mondo:0013052,retinitis pigmentosa 42,"['retinitis pigmentosa caused by mutation in KLHL7', 'retinitis pigmentosa 42', 'RP42', 'KLHL7 retinitis pigmentosa', 'retinitis pigmentosa type 42']",0110386,612943,,C2751986,,,,C567854,,H35.5,,
mondo:0013053,"microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type","['Hadziselimovic syndrome', 'microcephaly-faciocardioskeletal syndrome']",,612946,217026,C2751878,,,,C567850,,,,
mondo:0013054,"microcephaly, growth retardation, cataract, hearing loss, and unusual appearance","['microcephaly, growth retardation, cataract, hearing loss, and unusual appearance']",,612947,,C2751870,,,,C567849,,,,
mondo:0013055,"Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features","['Stargardt macular degeneration, absent or hypoplastic corpus callosum, intellectual disability, and dysmorphic features', 'Stargardt macular degeneration absent or hypoplastic corpus callosum intellectual disability and dysmorphic features', 'Stargardt macular degeneration absent or hypoplastic corpus callosum mental retardation and dysmorphic features', 'Stargardt macular degeneration, absent or hypoplastic corpus callosum, mental retardation, and dysmorphic features']",,612948,,C2751864,,,,C548086,,,,
mondo:0013056,"developmental and epileptic encephalopathy, 39","['EIEE39', 'AGC1 deficiency', 'mitochondrial aspartate-glutamate carrier 1 deficiency', 'epileptic encephalopathy with global cerebral demyelination', 'epileptic encephalopathy, early infantile, 39', 'early infantile epileptic encephalopathy caused by mutation in SLC25A12', 'hypomyelination, global cerebral', 'developmental and epileptic encephalopathy 39', 'aspartate-glutamate carrier 1 deficiency', 'SLC25A12 early infantile epileptic encephalopathy', 'DEE39']",0080349,612949,353217,C4512050,"['-0.42', '0.2776', '-0.03473', '-0.2313', '-0.1406', '-0.5815', '0.007355', '0.9883', '-0.8193', '-0.1844', '-0.557', '-0.3394', '0.1991', '-0.269', '0.2751', '-0.2047', '0.1382', '-0.2769', '-0.4836', '-0.6353', '0.0883', '-0.3755', '0.3135', '-0.01408', '0.1174', '-0.05798', '-0.0733', '-0.1562', '-0.3025', '-0.07825', '0.3545', '0.3086', '0.3406', '0.0927', '-0.1809', '0.6426', '-0.2185', '-0.281', '-0.1295', '0.1248', '0.0947', '-0.563', '-0.2124', '0.252', '-0.0854', '0.155', '-0.02788', '0.1418', '-0.2305', '0.1656', '-0.0316', '0.2384', '-0.301', '0.07715', '0.138', '-0.2145', '0.2062', '-0.1582', '-0.12274', '0.7246', '0.05588', '0.2239', '0.4604', '0.2032', '-0.2343', '-0.0332', '0.385', '0.2876', '-0.5117', '0.2395', '-0.1093', '-0.0269', '-0.212', '0.01714', '0.02946', '0.1356', '0.07776', '-0.11444', '-0.5', '0.182', '0.12177', '-0.013466', '-0.1343', '0.598', '0.0707', '-0.05975', '-0.1119', '0.393', '0.3503', '0.2642', '0.4487', '0.22', '0.398', '0.2162', '0.1256', '0.3804', '0.1978', '-0.4023', '0.4617', '-0.02655']",,,C567847,,,,
mondo:0013057,"psoriasis 12, susceptibility to","['psoriasis 12, susceptibility to', 'psoriasis susceptibility 12', 'PSORS12']",0111291,612950,,,,,,,,,,
mondo:0013058,cystic leukoencephalopathy without megalencephaly,"['RNAse T2-deficient leukoencephalopathy', 'leukoencephalopathy, cystic, without megalencephaly', 'CLWM']",0081007,612951,85136,C2751843,"['-0.131', '0.03662', '-0.1392', '-0.1047', '0.2189', '-0.0676', '-0.1624', '0.3513', '-0.4846', '-0.3054', '-0.5713', '-0.708', '-0.4233', '-0.375', '0.3467', '-0.1427', '0.05542', '-0.10657', '-0.2166', '-0.267', '-0.07837', '-0.1259', '-0.05508', '-0.4006', '0.3027', '-0.052', '-0.1592', '-0.0642', '0.3518', '0.1031', '0.1672', '-0.2235', '0.4292', '-0.1575', '0.4563', '0.0898', '-0.5034', '-0.3372', '-0.00524', '-0.086', '0.4778', '-0.1785', '-0.08', '-0.3982', '0.004635', '-0.05594', '-0.2479', '0.08514', '-0.3513', '-0.5283', '0.5293', '0.01329', '0.02988', '0.109', '-0.1311', '0.03802', '0.3376', '-0.2517', '-0.2502', '0.3455', '0.113', '0.1486', '0.1747', '-0.1116', '-0.4077', '-0.2712', '0.2827', '0.639', '-0.6235', '0.1947', '0.0989', '0.3752', '0.1056', '0.0418', '-0.0576', '0.2627', '0.39', '0.293', '-0.26', '-0.11615', '0.07416', '0.1426', '0.1901', '0.813', '-0.2227', '0.06726', '0.16', '0.397', '0.01869', '0.2019', '0.3794', '0.5913', '0.1122', '0.1212', '1.089', '-0.0726', '0.5283', '-0.568', '0.2703', '0.09644']",,,C567845,,,,
mondo:0013059,Aicardi-Goutieres syndrome 5,"['SAMHD1-related Aicardi-Goutieres syndrome', 'Aicardi-Goutieres syndrome 5', 'AGS5', 'Aicardi-Goutieres syndrome caused by mutation in SAMHD1', 'Aicardi-Goutieres syndrome type 5', 'SAMHD1 Aicardi-Goutieres syndrome']",,612952,,,,C168564,,C535608,,,,
mondo:0013060,autosomal recessive Parkinson disease 14,"['PARK14', 'dystonia-parkinsonism, Paisan-Ruiz type', 'dystonia-Parkinsonism, adult-onset', 'hereditary late onset Parkinson disease caused by mutation in PLA2G6', 'adult-onset dystonia - parkinsonism', 'PLA2G6-related dystonia-parkinsonism', 'autosomal recessive Parkinson disease type 14', 'dystonia-Parkinsonism Adult-onset', 'Parkinson disease 14, autosomal recessive', 'PLA2G6 hereditary late onset Parkinson disease', 'autosomal recessive Parkinson^s disease 14']",0060900,612953,199351,C2751842,"['-0.007042', '0.594', '-0.4275', '-0.3145', '-0.4175', '-0.615', '0.1346', '0.551', '-0.3682', '-0.5654', '0.05853', '0.2194', '-0.1035', '-0.2632', '0.827', '-0.0986', '0.03766', '-0.591', '-0.3462', '-0.74', '-0.3171', '-0.2556', '-0.1876', '-0.2874', '0.0763', '-0.4893', '-0.252', '0.1203', '0.003181', '0.1443', '0.1326', '0.3062', '0.433', '-0.4836', '0.5337', '-0.11066', '0.061', '-0.6504', '0.1511', '0.2063', '0.8486', '-0.292', '0.00732', '0.0372', '0.268', '-0.5864', '-0.4316', '0.004387', '0.1512', '0.0451', '0.2324', '0.6733', '-1.003', '-0.1252', '0.5537', '-0.446', '0.5874', '-0.3665', '-0.1344', '0.1609', '0.2632', '0.2167', '-0.0673', '-0.682', '-0.5874', '0.10443', '0.4365', '0.4414', '0.004757', '0.2214', '-0.694', '-0.0683', '0.06287', '0.225', '0.415', '0.3293', '-0.06396', '0.1768', '-0.4104', '-0.2139', '0.1815', '-0.45', '0.599', '0.4805', '-0.0442', '0.1907', '0.2776', '0.429', '0.648', '-0.0538', '0.2922', '0.3513', '0.5024', '0.3198', '0.4043', '0.3179', '0.1958', '-0.1595', '0.0901', '-0.07495']",,,C567844,,,,
mondo:0013061,myofibrillar myopathy 6,"['MFM6', 'myofibrillar myopathy type 6', 'BAG3 myofibrillar myopathy (disease)', 'myopathy, myofibrillar, 6', 'muscular dystrophy, Selcen type', 'BAG3-related myofibrillar myopathy', 'myopathy, myofibrillar, Bag3-related', 'myopathy, myofibrillar, type 6']",0080097,612954,199340,,"['-0.55', '0.0602', '0.08044', '-0.1637', '0.17', '-0.6787', '0.00956', '0.3147', '-0.4097', '-0.07916', '-0.3047', '-0.1083', '0.1031', '0.0659', '0.3162', '-0.08746', '-0.07556', '-0.1514', '-0.0862', '-0.333', '0.0811', '-0.2329', '0.2334', '0.1493', '-0.122', '0.04324', '0.1738', '-0.0935', '-0.3704', '0.1069', '0.2651', '0.1464', '0.1796', '0.09534', '0.0815', '-0.0737', '-0.1389', '-0.1459', '0.05148', '-0.3555', '-0.3213', '-0.3525', '-0.1432', '0.25', '-0.552', '0.3086', '-0.2081', '0.04883', '-0.2883', '-0.06464', '0.148', '0.08813', '0.2788', '0.1277', '-0.06012', '-0.693', '0.5215', '-0.1157', '-0.0869', '0.1852', '0.1595', '-0.165', '-0.0373', '-0.026', '-0.4404', '-0.3462', '0.3545', '0.825', '-0.3442', '0.0824', '-0.2089', '-0.005405', '0.2401', '0.09845', '0.2974', '0.01358', '-0.34', '0.2324', '-0.10944', '0.0764', '-0.02077', '0.11926', '0.0313', '0.3062', '-0.00784', '-0.06113', '0.2429', '0.3357', '0.372', '-0.2734', '0.472', '-0.10223', '0.2092', '0.382', '0.5444', '0.0107', '0.45', '-0.4634', '-0.1072', '0.1056']",,,C567843,,,,
mondo:0013062,long QT syndrome 12,"['long QT syndrome 12', 'long QT syndrome caused by mutation in SNTA1', 'LQT12', 'SNTA1 long QT syndrome', 'long QT syndrome type 12']",0110653,612955,101016,C2751830,"['-0.01378', '0.02745', '0.008224', '0.00457', '0.012405', '-0.05075', '0.01572', '0.0475', '-0.03204', '-0.03047', '0.007084', '0.00402', '0.003044', '0.002724', '-0.01674', '-0.02168', '0.00899', '-0.01256', '-0.002935', '-0.05588', '-0.00689', '-0.007782', '0.02876', '-0.0048', '0.01878', '-0.01988', '-0.002853', '0.003635', '0.01146', '-0.03062', '0.03806', '-0.015495', '0.02832', '0.01508', '0.002205', '-0.01591', '-0.01974', '-0.01308', '-0.01773', '-0.03912', '0.01174', '-0.0387', '0.02824', '-0.03041', '0.02275', '-0.02226', '-0.02202', '0.04205', '-0.005444', '0.01605', '-0.01026', '-0.0112', '0.001744', '0.006847', '-0.02896', '-0.01407', '0.01927', '0.003708', '-0.0413', '0.005756', '0.0228', '0.01717', '0.001433', '0.009514', '0.0001502', '-0.00973', '0.04044', '0.0255', '-0.03082', '0.03934', '-0.02606', '0.005917', '0.02623', '-0.02806', '0.006092', '0.014275', '0.002102', '-0.01336', '-0.02437', '-0.02362', '-0.003544', '0.002768', '-0.01304', '0.01907', '-0.00593', '0.006542', '0.002024', '0.02902', '0.0345', '0.009964', '0.01435', '0.02065', '0.002432', '0.01346', '0.06207', '0.02245', '0.04318', '-0.0645', '-0.003103', '-0.0002515']",,,C567842,,,,
mondo:0013063,"ventricular fibrillation, paroxysmal familial, 2","['VF2', 'ventricular fibrillation, paroxysmal familial, 2', 'DPP6 ventricular fibrillation (disease)', 'ventricular fibrillation, paroxysmal familial, type 2']",,612956,,C2751829,,,,C567841,,,,
mondo:0013064,multiple synostoses syndrome 3,"['multiple synostoses syndrome type 3', 'FGF9 multiple synostoses syndrome', 'multiple synostoses syndrome 3', 'multiple synostoses syndrome caused by mutation in FGF9', 'SYNS3']",0081319,612961,,C2751826,,,,C567839,,,,
mondo:0013065,premature ovarian failure 7,"['premature ovarian failure type 7', 'primary ovarian failure caused by mutation in NR5A1', 'adrenocortical insufficiency', 'premature ovarian failure 7', 'adrenal insufficiency, Nr5A1-related', 'Pof7', 'NR5A1 primary ovarian failure']",0080864,612964,,C2751825,,,,C567838,,,,
mondo:0013066,"46,XY sex reversal 3","['46,XY SEX reversal 3', '46,XY Sex reversal, partial or complete, Nr5A1-related', 'Sex reversal, XY, with or without adrenal failure', 'SRXY3', 'disorder of Sex development, 46,XY, Nr5A1-related', '46,XY Sex reversal type 3', '46,XY gonadal dysgenesis, partial or complete, with or without adrenal failure', '46XY sex reversal 3', '46,XY sex reversal 3']",0111772,612965,,,,,,,,,,
mondo:0013067,cataract 34 multiple types,"['cataract 34 multiple types with or without microcornea', 'cataract 34, multiple types, with or without microcornea', 'FOXE3 cataract (disease)', 'CTRCT34', 'CATC3', 'autosomal recessive congenital cataract 3', 'cataract 34, multiple types', 'cataract, autosomal recessive congenital 3']",0110230,612968,98993,C2751822,,,,C567835,,,,
mondo:0013068,age-related hearing impairment 2,"['ARHI2', 'age-related hearing impairment 2', 'presbycusis 2']",,612976,,C2751814,,,,C567834,,,,
mondo:0013069,"autosomal recessive optic atrophy, OPA7 type","['optic atrophy 7 with or without auditory neuropathy', 'optic atrophy 7', 'OPA7']",0111437,612989,227976,C2751812,"['-0.294', '0.1692', '0.0824', '-0.1895', '-0.1096', '-0.02611', '0.1458', '0.0967', '-0.2313', '0.06146', '0.1149', '-0.3997', '-0.4072', '-0.279', '-0.2532', '-0.642', '0.001796', '0.006996', '0.0782', '-0.5234', '0.305', '-0.4985', '-0.03726', '0.3203', '0.1736', '0.351', '-0.08435', '0.04517', '0.0488', '-0.1622', '0.04904', '0.2722', '0.6455', '0.277', '-0.02086', '-0.396', '-0.1121', '-0.5405', '0.0131', '-0.4424', '-0.02422', '-0.1832', '0.01459', '0.1382', '-0.1261', '-0.071', '0.1128', '-0.1571', '0.3901', '-0.0709', '0.1974', '0.1887', '-0.05072', '-0.6636', '0.1034', '-0.02216', '0.6973', '0.2466', '-0.4905', '0.2142', '-0.3381', '-0.05264', '0.10754', '0.2485', '-0.65', '0.1584', '0.1072', '1.111', '-0.1372', '0.5884', '-0.2443', '-0.10254', '0.2825', '-0.5044', '-0.1414', '-0.065', '0.2773', '0.4355', '-0.0683', '-0.1744', '0.10486', '-0.2817', '-0.1505', '0.603', '-0.1451', '-0.268', '0.2788', '0.3433', '0.002247', '0.2471', '0.3838', '-0.01703', '0.2252', '0.127', '0.986', '0.2157', '0.4465', '0.3398', '-0.0866', '0.1646']",,,C567833,,,,
mondo:0013070,spermatogenic failure 7,"['spermatogenic failure type 7', 'Male infertility, nonsyndromic, autosomal recessive', 'SPGF7', 'spermatogenic failure 7']",0070173,612997,,C2751811,,,,C567832,,,,
mondo:0013071,"Emery-Dreifuss muscular dystrophy 4, autosomal dominant","['SYNE1 autosomal dominant Emery-Dreifuss muscular dystrophy', 'autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in SYNE1', 'EMERY-Dreifuss muscular dystrophy 4, autosomal dominant', 'Emery-Dreifuss muscular dystrophy 4 with variable features', 'Emery-Dreifuss muscular dystrophy 4, autosomal dominant', 'EDMD4']",0070249,612998,,C2751807,,,,C567831,,,,
mondo:0013072,"Emery-Dreifuss muscular dystrophy 5, autosomal dominant","['autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in SYNE2', 'Emery-Dreifuss muscular dystrophy 5, autosomal dominant', 'SYNE2 autosomal dominant Emery-Dreifuss muscular dystrophy', 'EMERY-Dreifuss muscular dystrophy 5, autosomal dominant', 'EDMD5']",0070250,612999,,C2751805,,,,,,,,
mondo:0013073,"palmoplantar keratoderma, nonepidermolytic, focal 1","['nonepidermolytic palmoplantar keratoderma caused by mutation in KRT16', 'keratoderma, focal nonepidermolytic palmoplantar', 'palmoplantar keratoderma, nonepidermolytic, focal type 1', 'KRT16 nonepidermolytic palmoplantar keratoderma', 'palmoplantar keratoderma, nonepidermolytic, focal 1', 'focal nonepidermolytic palmoplantar keratoderma', 'Ppkfne', 'FNEPPK1', 'palmoplantar keratoderma, nonepidermolytic, focal']",0111709,613000,,,,,,,,,,
mondo:0013074,encephalocraniocutaneous lipomatosis,"['encephalocraniocutaneous lipomatosis, somatic mosaic', 'encephalocraniocutaneous lipomatosis', 'Haberland syndrome', 'ECCL', 'Fishman syndrome']",,613001,2396,C0406612,"['0.10297', '-0.04852', '0.1355', '-0.1907', '0.148', '-0.3987', '0.3135', '0.371', '-0.595', '-0.337', '-0.081', '0.164', '-0.722', '-0.3035', '-0.202', '0.2021', '0.1498', '0.0829', '0.231', '-0.1252', '-0.02261', '0.0983', '-0.1142', '0.2383', '-0.2622', '0.002432', '-0.307', '0.00899', '0.3801', '-0.1509', '0.8965', '-1.058', '0.927', '-0.6235', '-0.3538', '0.52', '-0.4958', '-0.2399', '0.0715', '-0.08453', '0.561', '-0.5103', '-0.04675', '-0.513', '0.6084', '-0.1002', '0.1035', '0.02745', '0.0862', '-0.332', '0.1781', '0.2695', '0.10693', '-0.1959', '-0.842', '0.1895', '-0.436', '0.5454', '-0.725', '0.27', '0.295', '-0.3718', '-0.4858', '0.4695', '-0.3992', '-0.1843', '0.09906', '1.159', '-0.2925', '0.59', '-0.253', '0.3079', '0.1527', '-0.1764', '0.085', '-0.02354', '0.1537', '0.85', '-0.3386', '-0.8066', '-0.00807', '0.3796', '0.7075', '0.12286', '0.772', '-0.389', '-0.0573', '0.2524', '-0.1141', '0.3767', '0.2341', '0.596', '0.1486', '0.2776', '0.582', '-0.1886', '0.2493', '-0.1772', '0.11145', '0.1165']",C4701,,C535736,757.8,,,
mondo:0013075,"herpes simplex encephalitis, susceptibility to, 2","['Herpes simplex encephalitis, susceptibility to, type 2', 'encephalopathy, acute, infection-induced, susceptibility to, 2', 'IIAE2', 'herpes simplex encephalitis, susceptibility to, 2', 'encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 2', 'encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 2']",,,,,,,,,,,,
mondo:0013076,"attention deficit-hyperactivity disorder, susceptibility to, 7","['attention deficit-hyperactivity disorder, susceptibility to, 7', 'attention Deficit-hyperactivity disorder, susceptibility to, type 7', 'susceptibility to attention deficit-hyperactivity disorder 7', 'ADHD7']",,613003,,,,,,,,,,
mondo:0013077,Santos syndrome,"['Santos syndrome', 'fibular agenesis/hypoplasia, oligodactylous clubfeet, and anonychia/nail hypoplasia syndrome']",,613005,,C2751698,,,,C567819,,,,
mondo:0013078,type 1 diabetes mellitus 24,"['diabetes mellitus, insulin-dependent, 24', 'insulin-dependent diabetes mellitus 24', 'IDDM24']",0110761,613006,,C2751697,,,,C567818,,,,
mondo:0013079,primary biliary cholangitis 2,"['biliary cirrhosis, primary, 2', 'PBC2']",0070359,613007,,C2751696,,,,C567817,,,,
mondo:0013080,primary biliary cholangitis 3,"['biliary cirrhosis, primary, 3', 'PBC3']",0070360,613008,,C2751695,,,,C567816,,,,
mondo:0013081,lymphoproliferative syndrome 1,"['LPFS1', 'ITK deficiency', 'lymphoproliferative syndrome 1', 'ITK lymphoproliferative syndrome', 'lymphoproliferative syndrome type 1', 'lymphoproliferative syndrome caused by mutation in ITK']",0060707,613011,538963,C3552634,,C126344,,C567815,,,,
mondo:0013082,Hirschsprung disease-ganglioneuroblastoma syndrome,"['neuroblastoma with Hirschsprung disease', 'Hirschsprung disease ganglioneuroblastoma']",,,635,C2751683,"['-0.6543', '0.2167', '0.718', '-0.08246', '-0.1109', '-0.078', '0.1589', '0.04425', '-0.4854', '-0.1571', '0.09766', '-0.3064', '-0.4702', '0.54', '-0.11365', '0.566', '-0.526', '-0.246', '0.3147', '-0.556', '0.2454', '-0.7173', '-0.2993', '-0.4658', '-0.08136', '-0.1495', '-0.1077', '0.2773', '0.4636', '-0.07227', '0.2637', '-0.216', '0.6055', '-0.3623', '-0.06885', '0.4404', '-1.03', '0.1565', '-0.10583', '-0.05746', '0.1982', '0.2103', '0.0010395', '-0.2449', '-0.6016', '0.0689', '-0.05447', '-0.04065', '0.4146', '0.0509', '0.1565', '0.11865', '0.02774', '0.04492', '-0.4502', '0.10944', '-0.639', '-0.1261', '-0.1917', '-0.271', '0.4702', '0.1604', '-0.278', '0.063', '-0.2783', '0.645', '0.536', '0.0958', '0.1895', '0.77', '-0.1853', '0.5557', '0.1876', '-0.1302', '0.1471', '0.4358', '0.1599', '1.018', '0.1512', '-0.5933', '-0.2222', '-0.3298', '0.01096', '-0.1703', '-0.152', '-0.4097', '1.13', '0.1292', '0.2644', '0.314', '-0.1261', '-0.4028', '-0.275', '0.601', '0.95', '-0.2195', '0.3872', '-0.59', '0.2905', '0.4285']",,,C538119,,,,
mondo:0013083,"neuroblastoma, susceptibility to, 3","['neuroblastoma, susceptibility to, type 3', 'neuroblastoma caused by mutation in ALK', 'NBLST3', 'susceptibility to neuroblastoma 3', 'ALK neuroblastoma', 'neuroblastoma, susceptibility to, 3']",,613014,635,,,,,,,,,
mondo:0013084,"neuroblastoma, susceptibility to, 4","['neuroblastoma, susceptibility to, 4', 'NBLST4']",,613015,635,,,,,,,,,
mondo:0013085,"neuroblastoma, susceptibility to, 5","['NBLST5', 'neuroblastoma, susceptibility to, 5']",,613016,635,,,,,,,,,
mondo:0013086,"neuroblastoma, susceptibility to, 6","['neuroblastoma, susceptibility to, 6', 'NBLST6']",,613017,635,,,,,,,,,
mondo:0013087,bronchiectasis with or without elevated sweat chloride 2,"['bronchiectasis with or without elevated sweat chloride 2', 'SCNN1A bronchiectasis', 'bronchiectasis caused by mutation in SCNN1A', 'bronchiectasis with or without elevated sweat chloride type 2', 'cystic fibrosis-like syndrome', 'BESC2']",0080527,613021,,C2751666,,,,C567813,,,,
mondo:0013088,"follicular lymphoma, susceptibility to, 1","['FL1', 'follicular lymphoma, susceptibility to, 1']",,613024,,,,,,,,,,
mondo:0013089,schizophrenia 13,"['schizophrenia 13', 'schizophrenia susceptibility locus, chromosome 15Q13-q14-related', 'schizophrenia, susceptibility to, 13', 'SCZD13', 'schizophrenia, Neurophysiologic defect 1N']",0070089,613025,,C2751663,,,,,,,,
mondo:0013090,chromosome 19q13.11 deletion syndrome,"['monosomy 19q13.11', 'chromosome 19q13.11 deletion syndrome, distal', '19q13.11 microdeletion syndrome', 'chromosome 19Q13.11 deletion syndrome, distal', 'Del(19)(q13.11)']",0060408,,217346,C4304577,,,,C567810,,,,
mondo:0013091,glycogen storage disease IXc,"['GSD type IXc', 'GSD type 9C', 'GSD9C', 'GSD IXc', 'PHKG2 glycogen storage disease', 'glycogen storage disease IXc', 'PHKG2-related glycogen storage disease type IX', 'glycogen storage disease type IXc', 'glycogen storage disease caused by mutation in PHKG2']",0111043,613027,,C2751643,,,,C567809,,,,
mondo:0013092,glioma susceptibility 2,"['glioma susceptibility 2', 'malignant glioma caused by mutation in PTEN', 'PTEN malignant glioma', 'glioma susceptibility type 2', 'GLM2']",,613028,,,"['0.0008097', '0.02286', '0.01499', '-0.009895', '0.0202', '-0.04544', '0.01718', '0.04086', '-0.0317', '-0.03796', '-0.01648', '0.006714', '-0.00459', '0.01072', '-0.01573', '-0.0222', '0.001929', '-0.01773', '-0.00789', '-0.06854', '0.00996', '-0.02278', '0.05103', '-0.01535', '-0.000586', '-0.0046', '-0.01051', '0.00592', '-0.001339', '-0.02599', '0.0486', '-0.0145', '0.04117', '0.003937', '0.01761', '-0.02089', '-0.03061', '-0.01807', '0.0006065', '-0.04526', '0.03604', '-0.03195', '0.02127', '-0.011894', '-0.0003352', '-0.04755', '0.005', '0.03644', '0.002947', '0.000977', '0.001938', '-0.01688', '0.01153', '-0.00841', '-0.02524', '-0.01692', '0.02739', '-0.01775', '-0.04718', '-0.001147', '0.03192', '0.00906', '-0.00782', '0.02547', '-0.006634', '0.0222', '0.04486', '0.04532', '-0.04932', '0.05502', '-0.012726', '0.00334', '0.01039', '-0.0341', '0.03647', '0.02199', '-0.01301', '0.01537', '-0.03406', '-0.03754', '-0.01797', '0.010124', '-0.01331', '0.0577', '-0.02478', '-0.001948', '0.02777', '0.02689', '0.0568', '-0.007034', '0.02077', '0.03546', '-0.002563', '-0.01225', '0.10376', '0.02455', '0.04642', '-0.04767', '-0.0222', '0.01138']",,,,,,,
mondo:0013093,glioma susceptibility 3,"['malignant glioma caused by mutation in BRCA2', 'GLM3', 'glioblastoma 3', 'glioma susceptibility type 3', 'BRCA2 malignant glioma', 'glioma susceptibility 3']",,613029,360,,"['-0.005447', '0.06494', '0.02231', '-0.00955', '0.06168', '-0.0996', '0.02289', '0.0654', '-0.04498', '-0.06274', '-0.01949', '0.02614', '-0.03302', '0.009766', '-0.03004', '-0.05383', '0.01729', '-0.04218', '-0.006737', '-0.11426', '-0.00763', '-0.04794', '0.0794', '-0.01683', '-0.01458', '-0.011765', '-0.02792', '0.003862', '-0.02824', '-0.03754', '0.07416', '-0.0195', '0.07227', '0.01202', '0.0056', '-0.04584', '-0.03836', '-0.0422', '-0.02107', '-0.0652', '0.04922', '-0.05075', '0.03836', '-0.05838', '-0.0138', '-0.0658', '0.0251', '0.05496', '0.007442', '0.001736', '-0.04047', '-0.011696', '0.0399', '-0.01614', '-0.03348', '-0.01384', '0.03522', '-0.04205', '-0.08875', '0.01535', '0.0679', '0.03934', '0.01904', '0.0484', '0.0083', '0.05447', '0.08264', '0.08435', '-0.0743', '0.1117', '-0.04294', '0.005493', '0.03378', '-0.0649', '0.04623', '0.0339', '-0.02188', '0.01825', '-0.03174', '-0.05972', '-0.00857', '-0.00443', '-0.02594', '0.0987', '-0.0513', '-0.0312', '0.07104', '0.07416', '0.09735', '0.000295', '0.02118', '0.0728', '-0.006573', '-0.015274', '0.1863', '0.05057', '0.086', '-0.0661', '-0.05246', '0.009125']",,,,,,,
mondo:0013094,glioma susceptibility 5,"['GLM5', 'glioma susceptibility 5']",,613030,,,,,,,,,,
mondo:0013095,glioma susceptibility 6,"['GLM6', 'glioma susceptibility 6']",,613031,,C2751639,,,,,,,,
mondo:0013096,glioma susceptibility 7,"['GLM7', 'glioma susceptibility 7']",,613032,,,,,,,,,,
mondo:0013097,glioma susceptibility 8,"['GLM8', 'glioma susceptibility 8']",,613033,,C2751637,,,,,,,,
mondo:0013098,noise induced hearing loss,"['noise-induced hearing loss', 'NIHL', 'hearing loss, noise-induced, susceptibility to']",,,,,,C34664,1001254,D006317,388.12,,,
mondo:0013099,"combined pituitary hormone deficiencies, genetic form","['familial congenital hypopituitarism', 'combined pituitary hormone deficiencies, genetic forms', 'genetic hypopituitarism', 'familial hypopituitarism', 'multiple pituitary hormone deficiencies, genetic forms', 'pituitary hormone deficiency, combined']",,,95494,,,,,,,E23.0,,
mondo:0013100,"atrial fibrillation, familial, 8","['atrial fibrillation, familial, 8', 'ATFB8']",,613055,,C2751607,,,,C567802,,,,
mondo:0013101,"basal cell carcinoma, susceptibility to, 2","['basal cell carcinoma, susceptibility to, 2', 'BCC2']",,613058,,C2751606,,,,,,,,
mondo:0013102,"basal cell carcinoma, susceptibility to, 3","['BCC3', 'basal cell carcinoma, susceptibility to, 3']",,613059,,C2751605,,,,,,,,
mondo:0013103,"epilepsy, idiopathic generalized, susceptibility to, 10","['GEFSP5, susceptibility to', 'epilepsy, juvenile myoclonic, susceptibility to', 'GEFS+, type 5, susceptibility to', 'generalized epilepsy with febrile seizures plus, type 5, susceptibility to', 'EIG10', 'susceptibility to idiopathic generalised epilepsy 10', 'epilepsy, juvenile myoclonic, susceptibility to, 7', 'epilepsy, idiopathic generalized, susceptibility to, 10', 'epilepsy, idiopathic generalized, 10', 'generalised epilepsy with febrile seizures plus, type 5, susceptibility to', 'susceptibility to idiopathic generalized epilepsy 10', 'GEFS+5, susceptibility to', 'epilepsy, idiopathic generalized, susceptibility to, type 10']",0111292,613060,,,,,,,,,,
mondo:0013104,"basal cell carcinoma, susceptibility to, 4","['BCC4', 'basal cell carcinoma, susceptibility to, 4']",,613061,,C2751602,,,,,,,,
mondo:0013105,"basal cell carcinoma, susceptibility to, 5","['basal cell carcinoma, susceptibility to, 5', 'BCC5']",,613062,,C2751601,,,,,,,,
mondo:0013106,"basal cell carcinoma, susceptibility to, 6","['basal cell carcinoma, susceptibility to, 6', 'BCC6']",,613063,,C2751600,,,,,,,,
mondo:0013107,"dermatitis, atopic, 7","['dermatitis, atopic, susceptibility to, 7', 'dermatitis, ATOPIC, 7', 'atopic dermatitis type 7', 'ATOD7']",0110103,613064,,C2751599,,,,C567796,,,,
mondo:0013108,"leukemia, acute lymphocytic, susceptibility to, 1","['T-cell acute lymphoblastic leukemia, somatic', 'leukemia, B-cell acute lymphoblastic, susceptibility to', 'leukemia, T-cell acute lymphoblastic, susceptibility to', 'leukemia, acute lymphoblastic', 'leukemia, T-cell acute lymphoblastic, somatic', 'leukemia, acute lymphocytic, susceptibility to, 1', 'leukemia, acute lymphocytic, Philadelphia chromosome positive, somatic', 'ALL', 'leukemia, acute lymphoblastic, somatic', 'leukemia, T-cell acute lymphocytic, somatic', 'leukemia, acute lymphoblastic, B-Hyperdiploid, susceptibility to', 'All1', 'leukemia, acute lymphoblastic, susceptibility to, 1']",,613065,,C2751595,,,,,,,,
mondo:0013109,"leukemia, acute lymphocytic, susceptibility to, 2","['ALL2', 'leukemia, acute lymphoblastic, susceptibility to, 2', 'leukemia, acute lymphocytic, susceptibility to, 2']",,613067,,C2751593,,,,,,,,
mondo:0013110,neurodegenerative syndrome due to cerebral folate transport deficiency,"['neurodegeneration due to cerebral folate TRANSPORT deficiency', 'cerebral folate deficiency syndrome', 'cerebral folate transport deficiency']",0050719,613068,217382,,"['-0.1377', '0.1428', '0.1267', '-0.007835', '0.06946', '-0.1301', '-0.1516', '0.086', '-0.07654', '-0.07935', '-0.12317', '-0.1141', '0.0162', '-0.0681', '0.03015', '-0.1519', '-0.0642', '0.04044', '-0.2006', '-0.3528', '-0.04904', '-0.1023', '0.1028', '0.01878', '-0.03574', '-0.10144', '0.006832', '-0.04398', '0.07904', '-0.08575', '0.07715', '0.04453', '0.2373', '0.1014', '0.01884', '-0.10443', '-0.01968', '-0.1302', '-0.03876', '-0.2106', '0.1101', '-0.2302', '0.03726', '-0.07227', '-0.1339', '-0.196', '0.0638', '0.09033', '0.0047', '0.01692', '0.01006', '-0.021', '0.0737', '0.0437', '-0.1383', '-0.02017', '0.1942', '-0.004932', '-0.1572', '0.0861', '0.112', '0.08136', '0.1323', '-0.0548', '0.0863', '-0.0008245', '0.2258', '0.0993', '-0.2349', '0.189', '-0.0912', '-0.0653', '-0.1681', '-0.0784', '-0.03955', '0.12054', '0.1504', '0.0629', '-0.0962', '-0.05222', '0.01924', '-0.02567', '-0.06354', '0.1906', '0.0632', '-0.02509', '0.01123', '0.0808', '0.2742', '-0.04138', '0.2023', '0.1387', '-0.10144', '-0.05963', '0.2388', '0.1354', '0.1257', '-0.1799', '0.001276', '0.1671']",,,C567791,266.2,,,
mondo:0013111,acute infantile liver failure due to synthesis defect of mtDNA-encoded proteins,"['acute infantile liver failure', 'TRMU infantile liver failure', 'transient infantile liver failure', 'acute infantile liver failure due to synthesis defect of mitochondrial DNA-encoded proteins', 'liver failure, infantile, transient', 'liver failure, transient infantile', 'infantile liver failure caused by mutation in TRMU', 'LFIT']",0080778,613070,217371,C3278664,"['-0.3325', '0.095', '-0.05804', '0.2089', '0.0504', '-0.2822', '-0.09485', '0.7334', '0.0172', '0.11066', '-0.11865', '-0.563', '-0.28', '0.12494', '-0.3555', '-0.1512', '0.073', '0.02354', '-0.0221', '-0.699', '0.1095', '-0.506', '0.7026', '-0.0887', '-0.06964', '-0.4404', '0.1287', '-0.04996', '-0.05722', '-0.5054', '-0.002535', '0.2583', '0.3418', '0.1089', '-0.177', '-0.1613', '-0.2861', '-0.313', '-0.1132', '0.0208', '-0.2065', '-0.5537', '0.07367', '0.1953', '-0.6367', '-0.009514', '-0.10016', '-0.02484', '-0.2037', '0.3208', '-0.1573', '-0.188', '0.03592', '-0.2712', '-0.1948', '-0.3818', '0.479', '-0.1257', '-0.1032', '0.2634', '0.376', '0.2852', '0.44', '-0.3174', '-0.1118', '-0.4036', '0.2046', '0.5063', '-0.695', '0.2993', '0.2258', '0.203', '-0.1036', '0.0913', '-0.07385', '0.3523', '0.4868', '-0.0702', '-0.11786', '0.2898', '-0.2313', '-0.2091', '-0.4722', '-0.35', '0.317', '0.1305', '0.2559', '0.1359', '0.3823', '-0.3457', '0.7324', '-0.0666', '-0.2961', '-0.1273', '0.753', '0.6323', '0.09735', '-0.5703', '0.1013', '-0.04553']",,,,,,,
mondo:0013112,bronchiectasis with or without elevated sweat chloride 3,"['bronchiectasis with or without elevated sweat chloride type 3', 'cystic fibrosis-like syndrome', 'bronchiectasis caused by mutation in SCNN1G', 'bronchiectasis with or without elevated sweat chloride 3', 'SCNN1G bronchiectasis', 'BESC3']",0080528,613071,,C2751324,,,,C567772,,,,
mondo:0013113,metaphyseal anadysplasia 2,"['MMP9 metaphyseal anadysplasia', 'metaphyseal anadysplasia caused by mutation in MMP9', 'MANDP2', 'metaphyseal anadysplasia type 2', 'metaphyseal anadysplasia 2']",,613073,,C2751322,,,,C567771,,,,
mondo:0013114,autosomal dominant nonsyndromic hearing loss 50,"['autosomal dominant nonsyndromic deafness type 50', 'deafness, autosomal dominant 50', 'autosomal dominant deafness 50', 'autosomal dominant nonsyndromic deafness 50', 'DFNA50', 'deafness, autosomal dominant type 50']",0110576,613074,,,,,,,,,,
mondo:0013115,RIN2 syndrome,"['MACS syndrome', 'tall forehead-sparse hair-skin hyperextensibility-scoliosis syndrome', 'RIN2 deficiency', 'tall forehead, sparse hair, skin hyperextensibility, and scoliosis', 'macrocephaly, alopecia, cutis laxa, and scoliosis', 'macrocephaly-alopecia-cutis laxa-scoliosis syndrome']",,613075,217335,C2751321,"['0.04953', '-0.02481', '-0.179', '-0.555', '0.1466', '-0.956', '-0.3167', '0.5425', '-0.2142', '0.456', '0.452', '-0.6074', '-0.2957', '0.1675', '-0.252', '0.259', '0.7075', '-0.11554', '-0.2808', '-0.5835', '-0.05643', '-0.02707', '0.3618', '0.04935', '0.1771', '0.01823', '-0.412', '-0.10425', '0.668', '-0.4236', '0.6094', '0.0526', '0.10626', '0.1225', '0.3772', '-0.41', '-0.506', '-0.44', '0.4023', '-0.924', '0.486', '-0.734', '-0.6274', '0.52', '0.5166', '-0.525', '-0.01274', '0.668', '0.2576', '-0.269', '0.2073', '0.2854', '0.1787', '0.7373', '-0.3435', '-0.485', '0.02995', '-0.1997', '-0.04178', '-0.1102', '0.2124', '0.5415', '-0.4119', '-0.1272', '0.4133', '-0.004467', '0.274', '0.32', '-0.3801', '0.837', '-1.149', '-0.00744', '-0.1738', '-0.1192', '-0.5605', '0.05615', '-0.1534', '0.02353', '-0.5312', '0.05167', '0.10846', '-0.1886', '0.0904', '0.33', '-0.0844', '0.1267', '-0.2947', '0.0419', '0.12115', '0.05667', '0.04504', '0.5405', '0.5605', '0.5513', '1.067', '-0.08923', '0.4126', '0.3484', '0.3574', '0.1548']",,,C567770,,,,
mondo:0013116,congenital cataract-progressive muscular hypotonia-hearing loss-developmental delay syndrome,"['myopathy, mitochondrial progressive, with congenital cataract and developmental delay', 'congenital cataract-progressive muscular hypotonia-deafness-developmental delay syndrome', 'mitochondrial Complex deficiency, combined', 'myopathy with cataract and combined respiratory chain deficiency', 'myopathy with cataract and combined respiratory-chain deficiency', 'myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay']",,613076,330054,C2751320,"['0.5195', '0.193', '0.4524', '0.6484', '-0.4346', '0.1322', '1.036', '0.999', '-0.362', '-0.743', '0.1969', '-0.02452', '-0.4814', '0.1547', '-0.49', '-0.6685', '-0.656', '0.00703', '-0.6357', '-0.3176', '-0.05768', '0.0644', '-0.4878', '0.7075', '0.9487', '0.1141', '-1.245', '-0.011826', '-0.9243', '-0.1996', '-0.1385', '-0.0402', '0.1353', '-0.03244', '-0.4336', '-0.1895', '-0.3774', '-0.688', '0.001031', '-0.679', '-0.01793', '-0.05524', '-0.3276', '0.07654', '-0.0173', '-0.4448', '0.02965', '0.7075', '0.1143', '-0.2668', '-0.296', '-0.4844', '-0.1693', '-0.01967', '0.4673', '0.5835', '-0.0788', '0.10297', '-0.4016', '0.5083', '-0.3347', '0.791', '-0.172', '0.342', '-0.392', '0.2296', '-0.602', '1.212', '-0.5117', '-0.2676', '0.05353', '0.5493', '1.162', '-0.9824', '0.708', '-0.2517', '1.029', '0.3171', '0.2335', '0.09204', '-0.03044', '-0.4956', '-0.5444', '0.6562', '0.3052', '-0.2305', '-0.08215', '1.375', '0.2274', '0.6714', '0.1599', '0.2903', '-0.2057', '0.6987', '0.732', '-0.04407', '-0.0885', '-1.074', '-0.4204', '-0.1224']",,,C567769,,,,
mondo:0013117,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5","['progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 5', 'progressive external ophthalmoplegia, autosomal dominant 5', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5', 'RRM2B progressive external ophthalmoplegia with mitochondrial DNA deletions', 'progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RRM2B', 'PEOA5']",0111518,613077,,C2751319,,,,C567768,,,,
mondo:0013118,Nijmegen breakage syndrome-like disorder,"['NBs-like disorder', 'Nijmegen breakage syndrome-like disorder', 'Rad50 deficiency', 'RAD50 deficiency', 'microcephaly and chromosomal instability without immunodeficiency', 'NBSLD', 'microcephaly and spontaneous chromosome instability without immunodeficiency']",,613078,240760,C2751318,"['-0.7227', '0.01142', '0.2175', '-0.684', '0.1118', '-0.2264', '0.5996', '0.1694', '-0.707', '-0.02101', '0.512', '0.3757', '0.2747', '-0.295', '-0.1577', '-0.04068', '0.4749', '0.002956', '-0.1604', '-0.303', '0.01352', '-0.04877', '0.202', '-0.6', '0.5854', '-0.0435', '-0.0204', '0.1357', '0.1942', '-0.305', '0.2915', '0.226', '0.7397', '0.2216', '-0.0313', '-0.1743', '-0.66', '-0.3787', '-0.59', '-0.4014', '0.226', '-0.1065', '-0.544', '-0.1544', '-0.1472', '-0.6963', '0.247', '0.4915', '0.0499', '-0.646', '-0.566', '0.0643', '-0.2676', '0.471', '-0.668', '0.0417', '-0.2568', '-0.3987', '-0.5723', '0.12054', '0.2042', '-0.1477', '-0.3232', '0.3796', '-0.2793', '0.1705', '0.6055', '0.1857', '-0.2101', '0.3894', '-0.5845', '0.1044', '0.0252', '0.01694', '-0.1796', '-0.1674', '0.1825', '-0.546', '0.1722', '-0.04395', '0.02509', '0.2083', '-0.3486', '0.3567', '-0.377', '-0.3135', '0.2445', '0.4758', '0.3865', '0.345', '0.278', '0.975', '-0.135', '-0.2252', '0.818', '0.4148', '0.666', '0.1296', '0.3203', '0.685']",C153178,,C567767,,,,
mondo:0013119,autosomal recessive nonsyndromic hearing loss 77,"['LOXHD1 autosomal recessive nonsyndromic deafness', 'autosomal recessive deafness 77', 'autosomal recessive nonsyndromic deafness type 77', 'deafness, autosomal recessive 77', 'DFNB77', 'autosomal recessive nonsyndromic deafness caused by mutation in LOXHD1', 'deafness, autosomal recessive type 77', 'autosomal recessive nonsyndromic deafness 77']",0110525,613079,,C2746083,,,,C567543,,,,
mondo:0013120,"46,XY sex reversal 5","['46,XY sex reversal 5', '46XY sex reversal 5', 'Sex reversal, XY, Cbx2-related', 'SRXY5', '46,XY SEX reversal 5', '46,XY Sex reversal, Cbx2-related', '46,XY gonadal dysgenesis, complete, Cbx2-related', '46,XY Sex reversal type 5', 'disorder of Sex development, 46,XY, Cbx2-related']",0111776,613080,,C2751317,,,,C567766,,,,
mondo:0013121,"glaucoma 3, primary congenital, C","['glaucoma 3, primary congenital, C', 'GLC3C']",,613085,,,,,,,,,,
mondo:0013122,"glaucoma 3, primary congenital, D","['glaucoma 3, primary congenital, D', 'glaucoma 3, primary congenital, type D', 'GLC3D']",,613086,,C2751316,,,,C567765,,,,
mondo:0013123,atrial septal defect 6,"['atrial heart septal defect type 6', 'TLL1 atrial heart septal defect', 'atrial heart septal defect caused by mutation in TLL1', 'atrial septal defect 6', 'ASD6', 'atrial septal defect type 6']",0110111,613087,,C2751315,,,,C567764,,,,
mondo:0013124,"pelvic organ prolapse, susceptibility to, 2","['pelvic organ prolapse, susceptibility to, type 2', 'Pvop2', 'pelvic organ prolapse, susceptibility to, 2']",,613088,,,,,,,,,,
mondo:0013125,CLAPO syndrome,"['CLAPO syndrome, somatic', 'capillary malformation of the LOWER LIP, lymphatic malformation of face and neck, asymmetry of face and limbs, and partial/generalized overgrowth', 'Clapo', 'Lopez-Gutierrez syndrome']",,613089,168984,C2751313,"['0.3157', '0.4565', '-0.256', '-0.3396', '-0.1359', '-0.6665', '0.1421', '0.1589', '-0.4602', '-0.444', '-0.02396', '-0.2277', '0.12335', '0.28', '-0.1567', '0.1963', '0.05792', '-0.727', '-0.465', '-0.1418', '-0.05518', '0.02316', '0.8857', '-0.5845', '0.2275', '0.1359', '-0.3247', '-0.0479', '0.2786', '-0.05554', '0.826', '-0.04648', '0.0768', '-0.03494', '0.3335', '0.2524', '0.0642', '-0.0714', '-0.3662', '-0.1982', '0.115', '-0.373', '-0.05765', '-0.2566', '0.299', '0.00775', '-0.1438', '0.705', '-0.09033', '-0.3154', '-0.2695', '-0.1349', '0.308', '0.1953', '-1.213', '-0.392', '0.1786', '-0.4019', '-0.1353', '-0.02386', '-0.1371', '-0.4116', '0.3542', '0.10913', '-0.4775', '0.08124', '0.4792', '-0.1355', '-0.4634', '0.2129', '-0.1074', '0.562', '0.4946', '0.3164', '-0.3333', '0.4834', '-0.05518', '0.115', '-0.0595', '-0.2212', '-0.621', '0.2634', '0.686', '0.4238', '0.118', '-0.2378', '0.1487', '0.374', '0.1917', '0.04276', '-0.1191', '0.6875', '0.066', '0.0459', '0.612', '-0.1367', '0.07715', '-0.676', '0.05215', '0.093']",,,C567763,,,,
mondo:0013127,asphyxiating thoracic dystrophy 3,"['SRTD3', 'short rib-polydactyly syndrome Saldino-Noonan type', 'short rib polydactyly syndrome Verma Naumoff type', 'polydactyly with neonatal chondrodystrophy type III', 'short rib-polydactyly syndrome type 1', 'polydactyly with neonatal chondrodystrophy, type I', 'Verma-Naumoff syndrome', 'SRPS1', 'SRPS type 1', 'short-rib thoracic dysplasia 3 with or without polydactyly', 'polydactyly with neonatal chondrodystrophy, type 3', 'short rib-polydactyly syndrome, type 2B', 'SRPS type 3', 'polydactyly with neonatal chondrodystrophy type 1', 'ATD3', 'asphyxiating thoracic dystrophy 3', 'short rib-polydactyly syndrome type 3', 'SRPS3', 'short rib-polydactyly syndrome type III', 'type I short rib polydactyly syndrome', 'short rib-polydactyly syndrome, type IIB', 'Saldino-Noonan syndrome', 'SRPS2B', 'asphyxiating thoracic dystrophy type 3']",0110087,613091,93271,C0432197,"['-0.631', '-0.2019', '0.101', '-0.4136', '0.594', '-0.552', '-0.538', '0.271', '-0.4287', '-0.4495', '-0.3394', '-0.226', '0.1284', '0.2386', '-0.4143', '-0.1203', '0.1151', '0.1622', '-0.2812', '-0.5415', '0.363', '-0.04074', '0.649', '-0.1528', '0.05887', '-0.0653', '-0.1033', '0.4797', '0.8345', '-0.2437', '0.8364', '-0.0806', '0.007477', '0.2183', '0.5312', '0.0316', '-0.2413', '-0.1549', '0.03998', '0.06116', '-0.2012', '-0.2384', '0.242', '-0.1849', '-0.1495', '-0.1871', '0.03955', '0.4678', '0.1512', '-0.1572', '0.001596', '0.2834', '-0.04816', '0.1736', '-0.3838', '-0.6904', '0.06647', '-0.066', '0.1621', '0.3457', '0.2651', '0.2157', '-0.3687', '0.1385', '-0.057', '-0.2361', '-0.093', '0.8413', '-0.551', '0.3792', '-0.1365', '-0.1337', '0.1605', '-0.06976', '-0.0919', '-0.03123', '-0.322', '0.316', '-0.1656', '-0.2544', '-0.5073', '0.05005', '0.02748', '0.09546', '-0.1427', '0.003256', '0.1843', '0.00973', '-0.13', '-0.1235', '-0.15', '-0.1737', '0.2944', '-0.0936', '0.763', '0.1597', '0.597', '-0.3242', '0.2534', '0.28']",C163755,,C537602,759.89,,,
mondo:0013128,familial juvenile hyperuricemic nephropathy type 2,"['familial juvenile hyperuricemic nephropathy caused by mutation in REN', 'autosomal dominant tubulointerstitial kidney disease due to mutations in REN', 'REN-associated FJHN', 'HNFJ2', 'ADTKD-REN', 'hyperuricemic nephropathy, familial juvenile, 2', 'REN-associated familial juvenile hyperuricemic nephropathy', 'early-onset hyperuricemia, Anemia, and progressive kidney failure', 'REN-associated kidney disease', 'familial juvenile hyperuricemic nephropathy type 2', 'hyperuricemic nephropathy, familial juvenile, type 2', 'tubulointerstitial kidney disease, autosomal dominant, 4', 'REN-related autosomal dominant tubulointerstitial kidney disease', 'FJHN type 2', 'REN familial juvenile hyperuricemic nephropathy']",,613092,217330,,"['-0.0747', '0.3662', '0.10565', '-0.1548', '-0.1398', '-0.627', '-0.1738', '0.0333', '-0.066', '-0.02693', '-0.00626', '-0.07465', '-0.4146', '-0.2861', '-0.0479', '-0.3765', '-0.0696', '0.09827', '0.1481', '-0.596', '0.0943', '-0.2455', '0.03586', '-0.1052', '-0.03506', '-0.2069', '-0.0272', '-0.241', '-0.1816', '-0.2932', '0.313', '0.2715', '0.306', '0.3943', '0.1786', '-0.3406', '-0.304', '-0.07623', '-0.2465', '-0.1185', '-0.1993', '-0.3928', '0.549', '0.02501', '-0.308', '-0.3782', '-0.1973', '-0.01108', '0.05774', '-0.1161', '0.04456', '0.3547', '0.2147', '-0.2595', '-0.1735', '-0.2852', '0.2452', '-0.04053', '-0.654', '0.2172', '0.3882', '0.1556', '0.2306', '-0.1917', '0.1062', '-0.423', '0.5757', '0.4402', '-0.3806', '0.08826', '-0.2295', '-0.2869', '0.0485', '-0.05698', '0.2218', '-0.2301', '-0.02983', '0.3926', '-0.2329', '0.0853', '-0.3142', '0.11115', '-0.04544', '0.2646', '0.208', '0.03062', '0.3628', '-0.03278', '0.001078', '0.11694', '0.538', '0.0444', '0.0284', '-0.3384', '0.4482', '0.4954', '0.565', '-0.3909', '-0.2031', '0.5034']",,,C567760,,,,
mondo:0013129,cone dystrophy 4,"['PDE6C cone dystrophy', 'achromatopsia 5', 'cone dystrophy type 4', 'cone dystrophy caused by mutation in PDE6C', 'cone dystrophy 4', 'COD4']",,613093,49382,,"['-0.3652', '-0.3396', '0.171', '0.0909', '0.2279', '-0.04532', '-0.1683', '0.6074', '-0.4087', '-0.6445', '0.0892', '-0.2172', '-0.6426', '0.2316', '0.3352', '-0.05588', '0.6406', '0.003626', '0.1476', '-0.537', '-0.8545', '-0.1342', '0.39', '0.1703', '-0.2249', '0.1786', '-0.3577', '0.476', '-0.1702', '0.376', '0.7065', '0.2622', '0.2211', '0.3699', '0.1904', '-0.3066', '-0.253', '-0.6377', '0.1847', '-0.2075', '0.7534', '-0.4087', '0.3577', '-0.275', '-0.327', '-0.5522', '-0.1114', '-0.549', '0.2722', '0.145', '0.4663', '-0.07697', '0.12476', '-0.4792', '-0.0706', '0.07214', '0.7363', '-0.1549', '-0.777', '-0.3257', '-0.3625', '0.11334', '0.5737', '0.2448', '0.0684', '-0.1218', '0.433', '0.3728', '-0.1169', '0.2808', '-0.2815', '0.01619', '-0.3079', '-0.502', '0.8223', '0.1815', '0.7383', '-0.6387', '0.0507', '0.2389', '0.6284', '-0.529', '-0.004265', '1.118', '-0.063', '0.00982', '-0.0728', '-0.0996', '0.2966', '-0.26', '0.19', '0.2081', '-0.617', '0.367', '0.559', '0.1032', '-0.2668', '-0.515', '0.1982', '0.782']",C164226,,C567758,,,,
mondo:0013130,isolated microphthalmia 4,"['isolated microphthalmia caused by mutation in GDF6', 'MCOP4', 'GDF6 isolated microphthalmia', 'microphthalmia, isolated 4', 'microphthalmia, isolated type 4', 'isolated microphthalmia type 4']",0060836,613094,,C2751307,,,,C567757,,,,
mondo:0013131,polycystic kidney disease 2,"['polycystic kidney disease 2 with or without polycystic liver disease', 'PKD2 autosomal dominant polycystic kidney disease', 'polycystic kidney disease, adult, type II', 'polycystic kidney disease type 2', 'polycystic kidney disease, adult, type 2', 'APKD2', 'autosomal dominant polycystic kidney disease caused by mutation in PKD2', 'PKD2', 'Autosomal dominant polycystic kidney disease type 2', 'polycystic kidney disease 2']",0110859,613095,,C2751306,,C123166,,,,,,
mondo:0013132,hereditary spastic paraplegia 36,"['spastic paraplegia 36, autosomal dominant', 'hereditary spastic paraplegia type 36', 'autosomal dominant spastic paraplegia 36', 'SPG36', 'autosomal dominant spastic paraplegia type 36']",0110787,613096,320365,C4510078,,,,C567930,,,,
mondo:0013133,"melanoma, cutaneous malignant, susceptibility to, 5","['melanoma, cutaneous malignant, susceptibility to, 5', 'melanoma, cutaneous malignant, susceptibility to, type 5', 'melanoma, cutaneous malignant, 5', 'susceptibility to cutaneous malignant melanoma 5', 'CMM5']",,613099,,,,,,,,,,
mondo:0013134,"glaucoma 1, open angle, O","['glaucoma 1, open angle, O', 'open-angle glaucoma caused by mutation in NTF4', 'GLC1O', 'NTF4 open-angle glaucoma', 'glaucoma 1, open angle, 1O', 'glaucoma 1, open angle, type O']",,613100,,C2751294,,,,C567753,,,,
mondo:0013135,familial hemophagocytic lymphohistiocytosis 5,"['STXBP2 genetic hemophagocytic lymphohistiocytosis', 'familial hemophagocytic lymphohistiocytosis type 5', 'hemophagocytic lymphohistiocytosis, familial, 5, with or without microvillus inclusion disease', 'genetic hemophagocytic lymphohistiocytosis caused by mutation in STXBP2', 'HLH5', 'HPLH5', 'hemophagocytic lymphohistiocytosis, familial, type 5', 'hemophagocytic lymphohistiocytosis, familial, 5', 'FHL5']",0110925,613101,540,C2751293,,,,C567752,,,,
mondo:0013136,hereditary hypotrichosis with recurrent skin vesicles,['hypotrichosis and recurrent skin vesicles'],,613102,217407,C2751292,"['-0.2666', '0.03146', '-0.2025', '-0.10956', '0.576', '-0.1624', '-0.3792', '0.02144', '-0.2161', '0.237', '0.01403', '0.2062', '0.1947', '-0.3074', '-0.3306', '0.2393', '0.553', '0.1575', '-0.3813', '-0.4602', '-0.2106', '-0.2482', '0.2827', '0.198', '0.2089', '0.4194', '-0.2673', '0.3083', '-0.2898', '-0.1815', '0.4106', '-0.04263', '-0.2507', '0.05725', '0.2283', '0.07245', '-0.3455', '0.3486', '0.2573', '-0.593', '0.4727', '-0.0475', '0.2925', '-0.387', '0.2805', '-0.754', '0.1277', '0.1323', '0.52', '-0.1951', '-0.8438', '-0.10254', '0.4011', '-0.04742', '-0.431', '-0.148', '0.3025', '-0.07025', '-0.1704', '-0.2218', '0.0957', '0.2062', '0.2544', '-0.3618', '0.073', '0.3245', '0.419', '0.3984', '-0.6885', '0.5693', '0.0677', '-0.0516', '-0.2172', '0.1361', '-0.441', '0.0324', '0.2489', '0.6226', '0.2384', '0.03754', '0.0946', '-0.4004', '0.2935', '0.1206', '0.0748', '-0.3342', '-0.3293', '0.404', '-0.0637', '0.412', '-0.01353', '0.4092', '0.04153', '0.2888', '0.763', '0.34', '0.4739', '-0.6357', '0.2915', '0.2708']",,,C567751,,,,
mondo:0013137,"choroidal dystrophy, central areolar 2","['choroidal dystrophy, central areolar 2', 'central areolar choroidal dystrophy caused by mutation in PRPH2', 'choroidal dystrophy, central areolar type 2', 'CACD2', 'macular dystrophy, progressive', 'PRPH2 central areolar choroidal dystrophy']",,613105,,C2751290,,,,C567750,,,,
mondo:0013138,"vertigo, benign recurrent, 2","['BRV2', 'vertigo, benign recurrent, 2']",,613106,,C2751289,,,,C567749,,,,
mondo:0013139,"neutropenia, severe congenital, 2, autosomal dominant","['SCN2', 'autosomal dominant severe congenital neutropenia caused by mutation in GFI1', 'neutropenia, severe congenital 2, autosomal dominant', 'GFI1 autosomal dominant severe congenital neutropenia', 'neutropenia, severe congenital, 2, autosomal dominant']",0112131,613107,,C2751288,,,,C567748,,,,
mondo:0013140,"candidiasis, familial, 4","['candidiasis, familial, type 4', 'candidiasis, familial chronic mucocutaneous', 'familial chronic mucocutaneous candidiasis caused by mutation in CLEC7A', 'CLEC7A familial chronic mucocutaneous candidiasis', 'candidiasis, familial, 4, autosomal recessive', 'CANDF4', 'candidiasis, familial, 4']",,613108,,C0341024,,,,,,,,
mondo:0013142,"neuropathy, hereditary sensory and autonomic, type 2B","['hereditary sensory and autonomic neuropathy type IIB', 'RETREG1 hereditary sensory and autonomic neuropathy type 2', 'hereditary sensory and autonomic neuropathy type 2B', 'HSAN2B', 'neuropathy, hereditary sensory and autonomic, type IIB', 'hereditary sensory and autonomic neuropathy type 2 caused by mutation in RETREG1']",0070150,613115,,C2751092,,,,,,,,
mondo:0013143,hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency,"['THPH11', 'hereditary thrombophilia due to congenital HRG deficiency', 'thrombophilia due to histidine-rich glycoprotein deficiency', 'thrombophilia 11 due to HRG deficiency', 'thrombophilia due to elevated histidine-rich glycoprotein']",0111903,613116,217467,,"['-0.526', '-0.1235', '-0.0007453', '-0.2632', '0.05066', '0.01678', '-0.1476', '-0.09436', '-0.2299', '0.3044', '0.07947', '0.2301', '0.0738', '0.0588', '-0.1781', '0.1782', '0.1616', '0.03087', '0.01323', '-0.4592', '-0.03497', '-0.01602', '0.3481', '0.1716', '0.02856', '0.1669', '0.181', '0.1167', '0.1718', '-0.1997', '0.1169', '0.0753', '0.4436', '0.2416', '-0.2422', '-0.2903', '-0.3428', '-0.0968', '-0.1484', '-0.11035', '0.03088', '-0.2369', '0.1439', '0.04395', '-0.0757', '-0.1696', '0.013794', '0.1545', '0.1254', '0.2172', '-0.169', '0.0455', '0.1422', '-0.0925', '-0.4592', '0.1588', '0.1954', '-0.04974', '-0.6123', '-0.0813', '-0.07745', '0.02477', '0.01154', '-0.06903', '0.07556', '0.143', '0.31', '0.454', '-0.2238', '0.2202', '-0.2954', '0.00848', '-0.1884', '-0.212', '0.435', '0.10474', '0.374', '0.0005507', '0.2527', '-0.1957', '-0.2098', '-0.1998', '-0.05338', '0.19', '0.0584', '0.0738', '-0.01921', '0.2289', '0.3064', '-0.3674', '0.167', '0.157', '0.0452', '-0.1293', '0.6187', '0.2256', '0.32', '-0.013985', '-0.0889', '0.284']",,,C567737,,,,
mondo:0013144,hereditary antithrombin deficiency,"['AT3D', 'hereditary antithrombin deficiency', 'hereditary thrombophilia due to congenital antithrombin deficiency', 'thrombophilia 7 due to antithrombin III deficiency', 'thrombophilia due to antithrombin III deficiency', 'antithrombin 3 deficiency', 'thrombophilia due to antithrombin 3 deficiency', 'congenital antithrombin III deficiency', 'hereditary thrombophilia due to congenital antithrombin 3 deficiency', 'congenital AT-III deficiency', 'AT III deficiency', 'antithrombin III deficiency', 'inherited antithrombin deficiency']",3755,613118,82,C0272375,"['-0.3467', '-0.09485', '-0.2932', '-0.4338', '-0.279', '-0.07117', '0.1652', '-0.0968', '0.0715', '-0.08734', '-0.1426', '0.1009', '0.2068', '-0.3328', '-0.459', '-0.2551', '0.2384', '0.0871', '0.02129', '-0.6147', '-0.12024', '-0.04816', '0.3965', '0.2527', '-0.07916', '0.02078', '0.2456', '0.404', '-0.0491', '-0.1166', '0.3833', '-0.05087', '0.2954', '0.02995', '-0.4553', '-0.1879', '0.1567', '0.03235', '0.2666', '-0.696', '-0.2986', '0.05664', '0.4653', '0.01888', '-0.08466', '-0.352', '0.1489', '0.484', '0.2479', '0.00587', '0.0889', '0.0642', '0.2588', '-0.3098', '-0.621', '-0.2249', '0.2212', '-0.00843', '-0.854', '0.3706', '-0.38', '0.1227', '0.4338', '-0.0859', '0.0945', '0.00921', '0.2296', '0.4368', '-0.5576', '0.2365', '-0.199', '0.1346', '-0.0947', '-0.1005', '0.4639', '-0.03099', '0.246', '0.0435', '0.1344', '-0.1017', '-0.3286', '-0.1653', '0.597', '0.1746', '-0.1654', '-0.2468', '0.00574', '-0.03635', '0.02052', '-0.316', '0.056', '0.1298', '-0.3943', '-0.1659', '0.5107', '0.8096', '0.661', '-0.3723', '-0.5566', '0.2239']",,,D020152,286.9,,,
mondo:0013145,Brugada syndrome 6,"['Brugada syndrome caused by mutation in KCNE3', 'Brugada syndrome 6', 'BRGDA6', 'Brugada syndrome type 6', 'KCNE3 Brugada syndrome']",0110223,613119,,C2751089,,,,C567735,,,,
mondo:0013146,Brugada syndrome 7,"['SCN3B Brugada syndrome', 'atrial fibrillation, familial, 16', 'Brugada syndrome caused by mutation in SCN3B', 'BRGDA7', 'Brugada syndrome 7', 'Brugada syndrome type 7']",0110224,613120,334,C2751088,"['0.2954', '0.5547', '-0.497', '0.009', '0.10876', '-0.11865', '0.569', '0.409', '0.4434', '-0.5605', '0.6235', '-0.2338', '0.2893', '0.428', '-0.2219', '-0.1898', '-0.878', '-0.10565', '-0.5757', '-0.4175', '0.2866', '0.665', '0.1691', '0.1157', '0.0582', '-0.629', '0.2483', '-0.0802', '0.7793', '-0.01539', '0.8394', '0.587', '0.3994', '0.5', '-0.2507', '-0.316', '-0.2415', '0.648', '0.75', '-0.625', '0.482', '0.1633', '0.2183', '0.443', '0.3713', '0.002333', '-0.2388', '-0.1366', '0.5146', '0.517', '0.1013', '0.5195', '-0.4124', '-0.4473', '0.04156', '-0.327', '-0.4224', '0.2783', '-0.7803', '-0.1355', '-0.226', '0.984', '0.011215', '-0.4397', '-0.298', '0.08276', '0.757', '0.923', '-0.5063', '0.1543', '0.1693', '0.8354', '0.267', '0.00258', '0.06647', '0.4016', '0.2153', '0.1478', '-0.5845', '-0.2405', '-0.1332', '-0.02574', '0.10126', '0.0641', '0.7646', '0.06003', '0.7266', '-0.07837', '0.2783', '0.2043', '0.111', '-0.1678', '-0.3408', '0.325', '0.834', '0.324', '0.1666', '-0.2979', '-0.973', '-0.1927']",,,C567734,,,,
mondo:0013147,dilated cardiomyopathy 1CC,"['cardiomyopathy, dilated, type 1Cc', 'dilated cardiomyopathy type 1CC', 'familial isolated dilated cardiomyopathy caused by mutation in NEXN', 'cardiomyopathy, dilated, 1CC', 'NEXN familial isolated dilated cardiomyopathy', 'CMD1CC']",0110424,613122,,C2751084,,,,C567733,,,,
mondo:0013148,Brugada syndrome 8,"['Brugada syndrome 8', 'Brugada syndrome type 8', 'BRGDA8', 'HCN4 Brugada syndrome', 'Brugada syndrome caused by mutation in HCN4']",0110225,613123,,C2751083,,,,C567732,,,,
mondo:0013149,"hydrops fetalis, nonimmune, with gracile bones and dysmorphic features","['hydrops fetalis, nonimmune, with gracile bones and dysmorphic features']",,613124,,C2751073,,,,C567731,,,,
mondo:0013150,"parkinsonism-dystonia, infantile","['IPD', 'Parkinsonism-dystonia infantile', 'dopamine transporter deficiency syndrome', 'PKDYS', 'PARKINSONISM-dystonia, infantile', 'infantile Parkinsonism-dystonia']",,,238455,C2751067,"['0.51', '0.1517', '-0.02113', '-0.5083', '-0.10535', '-1.178', '0.0679', '0.3572', '-0.807', '-0.03784', '1.019', '0.686', '-0.2869', '0.2344', '0.38', '0.7104', '-0.3706', '-1.019', '-0.6997', '-0.9062', '-0.3755', '-0.1417', '-0.1609', '-0.1539', '-0.2408', '0.11285', '-0.216', '0.245', '-0.4438', '-0.002886', '0.3025', '0.6387', '0.9985', '-0.2008', '0.4158', '0.3606', '0.5815', '-0.0926', '0.2433', '-0.1617', '0.4932', '-0.2423', '-0.5684', '0.308', '0.2466', '0.0426', '-0.2374', '-0.0404', '0.3674', '0.4023', '0.04913', '0.1431', '0.362', '0.03018', '0.6553', '-0.331', '-0.01877', '0.3994', '0.2505', '0.006916', '-0.5776', '-0.373', '0.03415', '-0.793', '-0.6924', '0.4695', '0.2423', '0.1775', '-0.2368', '0.5464', '-0.3232', '-0.4548', '-0.03867', '-0.06055', '0.04855', '0.763', '0.7734', '0.02338', '0.0609', '-0.1975', '0.279', '0.2986', '0.3604', '0.5312', '1.021', '0.4573', '0.2954', '0.323', '1.445', '-0.0766', '0.722', '0.2275', '0.361', '0.0908', '1.02', '0.2069', '-0.1682', '0.0232', '0.9214', '-0.4043']",C129866,,C567730,,,,
mondo:0013151,"choroidal dystrophy, central areolar, 3","['choroidal dystrophy, central areolar, 3', 'choroidal dystrophy, central areolar, with or without drusen', 'CACD3']",,613144,,C2751055,,,,C567729,,,,
mondo:0013152,"systemic lupus erythematosus, susceptibility to, 14","['SLEB14', 'systemic lupus erythematosus, susceptibility to, 14']",,613145,,,,,,,,,,
mondo:0013153,inflammatory bowel disease 28,"['inflammatory bowel disease 28, early onset, autosomal recessive', 'inflammatory bowel disease 28, autosomal recessive', 'early onset autosomal recessive inflammatory bowel disease 28', 'inflammatory bowel disease type 28', 'inflammatory bowel disease caused by mutation in IL10RA', 'IBD28', 'IL10RA inflammatory bowel disease', 'inflammatory bowel disease, early-onset, autosomal recessive']",0110899,613148,,C2751053,,C164676,,C567728,,,,
mondo:0013154,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2","['Walker-Warburg syndrome or muscle-eye-brain disease, Pomt2-related', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 2', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 2', 'muscle-eye-brain-POMT2 related', 'MDDGA2']",0111240,613150,899,C3150411,,C126742,,,,,,
mondo:0013155,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3","['muscular dystrophy, congenital, POMGNT1-related', 'muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 3', 'congenital muscular dystrophy-POMGNT1 related', 'muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 3', 'MDDGB3']",0112378,613151,,C3150412,,,,,,,,
mondo:0013156,"muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B4","['muscular dystrophy-dystroglycanopathy (congenital without intellectual disability), type B, 4', 'MDDGB4', 'congenital muscular dystrophy-FKTN related', 'muscular dystrophy-dystroglycanopathy (congenital without mental retardation), type B, 4', 'muscular dystrophy, congenital, Fktn-related']",0112379,613152,,C2751052,,,,,,,,
mondo:0013157,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5","['muscle-eye-brain-FKRP related', 'Walker-Warburg syndrome or muscle-eye-brain disease, FKRP-related', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 5', 'MDDGA5']",0111241,613153,899,C3150413,,,,,,,,
mondo:0013158,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A6","['muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 6', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 6', 'MDDGA6', 'Walker-Warburg syndrome or muscle-eye-brain disease, large-related']",0111242,613154,899,C3150414,,C126743,,,,,,
mondo:0013159,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B1","['muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 1', 'muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 1', 'muscular dystrophy, congenital, Pomt1-related', 'MDDGB1', 'congenital muscular dystrophy-POMT1 related']",0050588,613155,370968,C3150415,,,,,,,,
mondo:0013160,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2","['muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 2', 'MDDGB2', 'muscular dystrophy, congenital, Pomt2-related', 'congenital muscular dystrophy-dystroglycanopathy with intellectual disability type B2', 'congenital muscular dystrophy-dystroglycanopathy with mental retardation type B2', 'congenital muscular dystrophy-POMT2 related', 'muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 2']",0112380,613156,370968,C3150416,,C126690,,,,,,
mondo:0013161,autosomal recessive limb-girdle muscular dystrophy type 2O,"['LGMD2O', 'LGMD-POMGNT1 related', 'muscular dystrophy, limb-girdle, type 2O', 'POMGNT1 autosomal recessive limb-girdle muscular dystrophy', 'MDDGC3', 'muscular dystrophy-dystroglycanopathy, limb-girdle, POMGNT1-related', 'muscular dystrophy-dystroglycanopathy (limb-girdle) type C3', 'limb-girdle muscular dystrophy type 2O', 'muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMGNT1', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 3']",0110292,613157,206564,C3150417,"['-0.1744', '-0.831', '-0.2423', '-0.363', '0.4504', '-1.231', '0.1086', '0.7627', '-1.759', '-0.9375', '0.2186', '0.4475', '-0.2842', '0.9863', '0.2443', '0.1857', '-0.7886', '-0.5273', '-0.472', '-0.905', '0.08417', '0.364', '0.2808', '0.684', '0.0444', '0.09924', '-0.3328', '-0.9497', '0.1407', '-0.277', '0.8115', '-0.1523', '0.4724', '0.02478', '0.2646', '0.01291', '-0.8374', '0.1103', '0.0746', '-0.4812', '0.2825', '-0.1382', '-0.5337', '0.1157', '-0.0344', '0.529', '0.2527', '0.7627', '-0.2651', '0.6514', '0.3945', '-0.37', '0.534', '-0.8716', '0.1005', '-0.7573', '0.521', '1.112', '-0.2299', '-0.1746', '0.2812', '-0.0634', '0.0453', '-0.1074', '-0.0923', '0.2576', '0.3557', '0.512', '-0.2247', '-0.0688', '-0.3323', '0.344', '0.2207', '-0.1405', '0.5454', '0.5015', '-0.2443', '0.3574', '-0.02225', '-0.10944', '0.187', '-0.005302', '0.01055', '0.2932', '-0.2576', '0.1065', '-0.1649', '-0.6816', '0.994', '0.308', '-0.3386', '0.1599', '0.4338', '1.024', '-0.0629', '-0.00252', '0.5073', '-0.5376', '-0.132', '-0.0807']",,,,,,,
mondo:0013162,autosomal recessive limb-girdle muscular dystrophy type 2N,"['muscular dystrophy-dystroglycanopathy limb-girdle POMT2-related', 'limb-girdle muscular dystrophy type 2N', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in POMT2', 'muscular dystrophy, limb-girdle, type 2N', 'POMT2 autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy-dystroglycanopathy, limb-girdle, Pomt2-related', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 2', 'LGMD2N', 'muscular dystrophy-dystroglycanopathy (limb-girdle) type C 2', 'MDDGC2', 'LGMD-POMT2 related']",0110298,613158,206559,C3150418,"['-0.0469', '-0.4033', '-0.4333', '-0.5444', '0.672', '-1.252', '0.04742', '0.818', '-1.702', '-0.7363', '0.11633', '0.534', '-0.1323', '0.9253', '0.02617', '0.4412', '-0.7354', '-0.6997', '-0.513', '-0.898', '-0.001098', '0.2544', '0.4602', '0.66', '0.3809', '-0.03452', '-0.09436', '-0.8726', '0.3408', '-0.5093', '0.6655', '-0.2012', '0.6865', '0.1869', '0.02623', '-0.0578', '-0.677', '0.3967', '0.06464', '-0.6387', '0.2947', '-0.346', '-0.673', '0.2139', '-0.365', '0.1405', '-0.091', '0.4873', '0.01509', '0.4124', '0.3792', '-0.3145', '0.315', '-0.946', '0.4312', '-0.822', '0.3223', '0.9097', '-0.1142', '-0.06027', '0.2637', '0.1754', '-0.2712', '-0.0843', '0.03195', '0.1608', '-0.04147', '0.6973', '-0.2966', '-0.3323', '-0.2162', '0.3274', '0.07245', '-0.0643', '0.605', '0.536', '0.05536', '0.4412', '-0.03003', '0.04163', '-0.1879', '0.3357', '0.003798', '0.2036', '-0.2664', '0.1709', '-0.2026', '-0.4312', '0.9263', '0.143', '-0.3193', '0.09906', '0.288', '0.9033', '-0.1809', '-0.00863', '0.4067', '-0.5654', '0.0153', '0.0306']",,,,,,,
mondo:0013163,nephronophthisis-like nephropathy 1,"['XPNPEP3 nephronophthisis (disease)', 'NPHPL1', 'NPHP-XPNPEP3', 'nephronophthisis-like nephropathy type 1', 'nephronophthisis-like nephropathy 1']",0111117,613159,,C3150419,,,,,,,,
mondo:0013164,beta-ureidopropionase deficiency,"['UPB1D', 'beta-ureidopropionase deficiency', 'BETA-ureidopropionase deficiency', 'Beta-alanine synthase deficiency']",,613161,65287,C1291512,"['-0.2089', '0.258', '-0.05795', '-0.0777', '0.1611', '-0.1888', '-0.0497', '0.3125', '-0.05853', '-0.111', '0.04742', '-0.06384', '0.005054', '-0.2778', '0.1063', '-0.02174', '0.04907', '0.0472', '-0.2212', '-0.3638', '-0.04468', '-0.05774', '0.3818', '-0.4463', '0.01095', '-0.09845', '-0.1175', '-0.10156', '0.1247', '-0.2177', '0.1467', '-0.0673', '0.3364', '0.28', '-0.1388', '-0.256', '-0.1614', '-0.3333', '-0.323', '-0.00688', '0.1353', '-0.4219', '-0.03662', '-0.3997', '-0.1619', '-0.2394', '0.0507', '0.2443', '-0.0816', '0.07495', '-0.042', '0.1599', '-0.2727', '0.11383', '-0.1543', '-0.0332', '0.05017', '-0.2347', '-0.1317', '0.1572', '0.2676', '0.03842', '0.2274', '0.003454', '0.1605', '-0.01182', '0.1714', '0.2356', '-0.442', '0.1556', '-0.00802', '-0.00106', '-0.0246', '0.08264', '0.1223', '0.277', '0.1906', '-0.22', '-0.02394', '-0.1559', '0.04172', '0.0876', '-0.006157', '0.2937', '0.3035', '0.215', '-0.01051', '0.2029', '0.369', '-0.136', '0.2428', '0.3137', '-0.32', '-0.1447', '0.4053', '0.3328', '0.3745', '-0.3042', '0.1414', '0.259']",,,C563210,277.6,,,
mondo:0013165,hereditary spastic paraplegia 45,"['autosomal recessive spastic paraplegia type 45', 'NT5C2 autosomal recessive complex spastic paraplegia', 'autosomal recessive complex spastic paraplegia caused by mutation in NT5C2', 'autosomal recessive spastic paraplegia 45', 'autosomal recessive spastic paraplegia type 65', 'SPG65', 'hereditary spastic paraplegia type 45', 'spastic paraplegia 45, autosomal recessive', 'SPG45']",0110797,613162,320396,CN203996,"['-0.3115', '-0.0506', '-0.04666', '-0.6597', '0.1611', '-0.7495', '-0.3225', '0.541', '-0.757', '-0.415', '-0.154', '0.1236', '-0.08264', '-0.0988', '0.594', '-0.00852', '0.2134', '-0.506', '-0.11847', '-0.725', '0.2384', '0.04352', '0.0445', '0.208', '0.2734', '0.5024', '0.02457', '0.364', '-0.06976', '-0.2722', '0.247', '-0.01854', '0.2551', '0.2659', '0.04105', '-0.2578', '-0.4128', '-0.4553', '0.257', '-0.3982', '0.0898', '-0.536', '-0.1514', '0.4731', '-0.1655', '-0.3628', '-0.2323', '0.08844', '0.04007', '-0.02652', '-0.1898', '0.3792', '-0.468', '-0.1575', '-0.2983', '-0.262', '0.3855', '-0.3826', '-0.2917', '0.3577', '-0.3398', '0.002726', '0.3757', '0.3608', '-0.5073', '0.4387', '0.4153', '0.6714', '-0.1425', '0.5024', '-0.377', '0.4275', '0.1251', '-0.31', '0.567', '0.4202', '0.03152', '0.3967', '0.1465', '-0.11096', '-0.159', '0.2345', '0.7734', '0.6704', '-0.1481', '0.1279', '-0.2357', '0.407', '0.03745', '0.1799', '0.2196', '0.182', '0.312', '0.1772', '0.6704', '0.4634', '0.656', '0.268', '-0.0777', '0.0421']",,,,,,,
mondo:0013166,GABA aminotransaminase deficiency,"['GABA transaminase deficiency', 'gamma aminobutyrate transaminase deficiency', '4 alpha aminobutyrate transaminase deficiency', 'GABAT', 'gamma aminobutyric acid transaminase deficiency', 'ABAT', 'GABA-transaminase deficiency', 'gamma-amino butyric acid transaminase deficiency', 'gamma-aminobutyric acid transaminase deficiency']",0060174,613163,2066,C0342708,"['-0.395', '0.4521', '-0.03102', '-0.3735', '0.01331', '-0.54', '-0.1945', '0.4175', '-0.2333', '-0.508', '-0.405', '-0.2788', '-0.04163', '-0.1587', '0.0645', '0.1392', '0.282', '-0.3367', '-0.287', '-0.5903', '-0.2206', '-0.02054', '0.2053', '-0.2876', '0.2006', '-0.1765', '-0.1516', '-0.2222', '-0.2164', '-0.2313', '-0.03387', '0.0833', '0.617', '0.2322', '-0.3523', '0.1483', '-0.3901', '-0.4219', '-0.4878', '0.02533', '0.1582', '-0.6445', '-0.11926', '-0.0988', '0.002874', '-0.1592', '0.1587', '-0.0755', '-0.4763', '0.3584', '0.003162', '0.069', '-0.2325', '0.1143', '-0.0517', '0.0276', '0.2354', '-0.2861', '-0.2125', '0.72', '-0.005993', '0.0394', '0.2012', '0.1317', '0.07227', '-0.039', '0.385', '-0.0356', '-0.1943', '0.2578', '-0.02908', '0.289', '-0.2927', '0.1342', '0.0378', '0.4492', '0.0958', '-0.1742', '-0.1791', '0.01845', '0.554', '0.5244', '-0.2683', '0.011826', '0.858', '0.4258', '0.05994', '0.1164', '0.7583', '0.2942', '0.4072', '0.6416', '0.00472', '0.3022', '0.466', '0.746', '0.1385', '-0.11017', '0.531', '0.07153']",,,C535407,,,,
mondo:0013167,parkinson disease 16,"['Parkinson disease 16', 'PARK16']",,613164,,C2751012,,,,C567726,,,,
mondo:0013168,dilated cardiomyopathy 1DD,"['dilated cardiomyopathy type 1DD', 'CMD1DD', 'RBM20 familial isolated dilated cardiomyopathy', 'familial isolated dilated cardiomyopathy caused by mutation in RBM20', 'cardiomyopathy, dilated, type 1Dd', 'cardiomyopathy, dilated, 1DD']",0110447,613172,,C2750995,,,,C567725,,,,
mondo:0013169,chromosome 5p13 duplication syndrome,"['chromosome 5p13 duplication syndrome', '5p13 microduplication syndrome', 'chromosome 5p13 duplication syndrome, isolated cases', 'trisomy 5p13', 'dup(5)(p13)']",0060460,613174,329802,C2750805,,,,C567717,,,,
mondo:0013170,"cutis laxa with severe pulmonary, gastrointestinal and urinary anomalies","['ARCL1C', 'autosomal recessive cutis laxa type IC', 'cutis laxa, autosomal recessive, type 1C', 'cutis laxa, autosomal recessive, type IC', 'autosomal recessive cutis laxa type 1C', 'cutis laxa with Severe pulmonary, gastrointestinal, and urinary abnormalities', 'Urban-Rifkin-Davis syndrome']",0070139,613177,221145,C2750804,"['-0.2637', '-0.2412', '0.0676', '-0.556', '0.557', '-0.605', '-0.1782', '0.1758', '-0.7085', '0.3533', '-0.5913', '-0.429', '-0.006344', '-0.3745', '-0.1649', '0.05692', '-0.002895', '-0.2805', '-0.3582', '-0.696', '0.1846', '-0.05313', '0.5215', '0.00155', '-0.2014', '0.1754', '-0.04608', '0.1577', '0.5347', '-0.2505', '0.4875', '0.2339', '0.2788', '-0.2406', '0.2727', '-0.819', '-0.5083', '-0.2299', '0.3428', '-0.4998', '-0.02383', '-0.4146', '0.2583', '0.4731', '0.08215', '0.1205', '-0.1417', '0.03253', '0.179', '-0.0487', '-0.2727', '0.2825', '0.4346', '0.2483', '-0.606', '-0.2798', '0.00409', '0.3596', '-0.129', '-0.002804', '0.1038', '0.4824', '0.1678', '0.1371', '0.3716', '0.05902', '0.473', '0.1465', '-0.509', '0.4343', '-0.7', '-0.5083', '-0.1627', '-0.06415', '0.0837', '-0.3516', '0.25', '0.3826', '0.01411', '-0.334', '-0.4055', '-0.12317', '0.1536', '0.1553', '-0.3472', '0.1619', '0.1283', '0.8003', '0.1473', '-0.146', '0.0444', '0.2043', '0.1316', '-0.3242', '0.706', '0.0642', '0.584', '-0.2666', '0.1506', '0.1876']",,,C567716,,,,
mondo:0013171,purine nucleoside phosphorylase deficiency,"['immunodeficiency due to purine nucleoside phosphorylase deficiency', 'purine-nucleoside phosphorylase deficiency', 'nucleoside phosphorylase deficiency', 'deficiency of inosine phosphorylase', 'PNPase deficiency', 'purine nucleoside phosphorylase deficiency', 'PNP deficiency']",5813,613179,760,C0268125,"['0.0981', '0.1581', '0.02103', '0.02884', '0.1268', '-0.4912', '0.475', '0.3218', '0.1143', '-0.5957', '-0.7017', '-0.24', '-0.3335', '0.257', '-0.03186', '-0.9307', '-0.1738', '0.2057', '-0.6304', '-0.5396', '-0.1519', '-0.6675', '0.3596', '-0.1305', '-0.5054', '-0.2905', '-0.518', '0.0534', '-0.705', '-0.1285', '0.10345', '0.41', '0.566', '-0.02211', '-0.267', '-0.2954', '-0.5005', '-0.2212', '-0.2905', '0.2069', '-0.3933', '-0.1737', '0.2874', '-0.1097', '0.1571', '-0.4617', '-0.1799', '-0.7876', '-0.381', '0.534', '0.2805', '0.2496', '0.08746', '0.5234', '-0.01636', '0.00714', '-0.0683', '-0.624', '0.1614', '0.077', '0.3337', '0.6167', '-0.2424', '0.825', '0.7124', '0.002382', '0.316', '0.3264', '-0.456', '0.0699', '-0.1213', '-0.575', '-0.694', '0.1742', '0.747', '0.1087', '0.2201', '-0.1368', '0.1436', '0.364', '-0.09644', '-0.4814', '0.1384', '0.5327', '0.2961', '0.5396', '-0.1487', '0.2035', '0.6523', '0.082', '0.865', '0.565', '-0.2966', '-0.3997', '0.7417', '0.9414', '0.1766', '0.04993', '0.2878', '-0.1948']",C3963,,C562587,277.2,,,
mondo:0013172,polymicrogyria with optic nerve hypoplasia,"['CDCBM8', 'cortical dysplasia, Complex, with Other brain malformations 8', 'polymicrogyria with optic nerve hypoplasia', 'cortical dysplasia, complex, with other brain malformations 8']",,613180,250972,C2750798,"['-0.3293', '0.1063', '0.4946', '-0.1632', '0.3442', '-0.08716', '-0.07214', '0.3298', '-0.536', '-0.2369', '-0.4604', '-0.874', '-0.286', '-0.635', '0.02917', '0.08466', '0.31', '-0.575', '-0.3562', '-0.4182', '0.497', '-0.1705', '0.2798', '0.02101', '0.238', '-0.3154', '-0.1418', '0.1921', '0.1625', '-0.1263', '0.4932', '0.302', '0.4146', '0.10876', '0.2842', '-0.0599', '-0.2272', '0.1024', '-0.0934', '-0.3552', '0.11145', '-0.238', '0.02365', '-0.184', '0.01426', '-0.339', '0.2396', '0.04666', '0.1772', '0.127', '-0.1891', '0.3826', '-0.2072', '0.1819', '-0.5723', '-0.03494', '-0.0461', '-0.03394', '-0.3745', '0.31', '-0.011696', '-0.1625', '0.0861', '0.4302', '-0.466', '0.1484', '0.3916', '0.563', '-0.698', '0.4917', '-0.1519', '0.3484', '0.2883', '0.06064', '-0.10657', '-0.404', '0.685', '0.644', '-0.41', '-0.1361', '0.1394', '-0.006763', '-0.04654', '0.617', '-0.12103', '-0.566', '0.04788', '0.4436', '-0.009605', '0.2827', '0.239', '0.4255', '0.1349', '-0.02625', '0.6885', '0.02458', '0.5146', '-0.4048', '0.551', '0.4268']",,,C567715,,,,
mondo:0013173,"intellectual disability, autosomal recessive 13","['mental retardation, autosomal recessive 13', 'TRAPPC9 autosomal recessive non-syndromic intellectual disability', 'intellectual disability, autosomal recessive 13', 'autosomal recessive non-syndromic intellectual disability caused by mutation in TRAPPC9', 'MRT13', 'intellectual disability, autosomal recessive type 13', 'mental retardation, autosomal recessive type 13']",0081098,613192,,C2750791,,,,C567714,,,,
mondo:0013174,primary ciliary dyskinesia 13,"['ciliary dyskinesia, primary, 13, with or without situs inversus', 'primary ciliary dyskinesia type 13', 'ciliary dyskinesia, primary, 13', 'DNAAF1 primary ciliary dyskinesia', 'CILD13', 'ciliary dyskinesia, primary, type 13', 'primary ciliary dyskinesia caused by mutation in DNAAF1', 'primary ciliary dyskinesia 13 with or without situs inversus']",0110618,613193,,C2750790,,,,C567713,,,,
mondo:0013175,retinitis pigmentosa 50,"['retinitis pigmentosa-50', 'RP50', 'BEST1 retinitis pigmentosa', 'retinitis pigmentosa type 50', 'retinitis pigmentosa 50', 'retinitis pigmentosa caused by mutation in BEST1', 'retinitis pigmentosa, concentric']",0110396,613194,,,,,,C567712,,H35.5,,
mondo:0013176,"Weill-Marchesani 4 syndrome, recessive","['15q26.3 microdeletion syndrome', 'ichthyosis-short stature-brachydactyly-microspherophakia syndrome', 'Weill-Marchesani syndrome 4', 'Weill-Marchesani-like syndrome', 'WMS4']",,613195,363992,C2750787,"['-0.3381', '0.1324', '0.1945', '-0.128', '0.306', '-0.3464', '-6.57e-05', '0.3323', '-0.128', '-0.3083', '-0.07605', '-0.01628', '-0.09064', '-0.0935', '-0.3174', '0.03897', '0.1406', '-0.06287', '-0.0842', '-0.503', '-0.0755', '0.294', '0.2223', '-0.02094', '-0.05295', '0.1559', '-0.01527', '0.0878', '0.1809', '0.03668', '0.11145', '-0.0758', '0.2499', '0.295', '-0.00806', '-0.09314', '0.1054', '-0.2208', '0.004', '-0.3232', '0.0761', '-0.1432', '0.0432', '0.1788', '-0.04303', '0.1467', '-0.0958', '0.3745', '0.148', '-0.183', '-0.09106', '-0.097', '0.1553', '-0.1417', '-0.11505', '-0.331', '0.1771', '-0.1427', '-0.0741', '-0.149', '0.3774', '0.07996', '-0.3433', '0.0821', '0.05814', '-0.1879', '0.3862', '0.3052', '-0.2795', '0.2603', '-0.3425', '-0.01283', '0.05234', '-0.2573', '-0.2083', '-0.12225', '0.087', '-0.03084', '-0.1635', '-0.04752', '-0.001805', '0.10724', '-0.2715', '0.2285', '-0.096', '0.09955', '0.0663', '0.315', '0.005054', '0.10944', '0.10693', '0.294', '0.2401', '0.2344', '0.52', '-0.03787', '0.3176', '-0.2136', '0.204', '0.10077']",,,C567710,,,,
mondo:0013177,congenital muscular dystrophy due to integrin alpha-7 deficiency,"['muscular dystrophy, congenital, due to integrin ALPHA-7 deficiency', 'congenital muscular dystrophy with ITGA7 deficiency', 'congenital muscular dystrophy with integrin alpha-7 deficiency', 'congenital myopathy due to integrin alpha-7 deficiency', 'ITGA7 congenital muscular dystrophy', 'muscular dystrophy, congenital, due to ITGA7 deficiency', 'congenital muscular dystrophy caused by mutation in ITGA7', 'myopathy, congenital, due to integrin Alpha-7 deficiency']",0110639,613204,34520,C2750786,"['-0.433', '-0.66', '-0.3728', '-0.2428', '0.6543', '-1.179', '0.1348', '0.596', '-1.8', '-0.5537', '0.2018', '0.544', '-0.3252', '0.62', '0.4463', '0.09174', '-0.8467', '-0.2554', '-0.479', '-0.7666', '0.447', '0.1532', '0.352', '0.7285', '0.342', '0.02931', '-0.2908', '-0.786', '0.05124', '-0.2842', '0.888', '0.2065', '0.5894', '-0.1711', '0.0396', '-0.5166', '-0.2927', '0.4607', '0.3623', '-0.5005', '0.08856', '-0.2338', '-0.527', '0.538', '-0.3906', '0.3738', '0.001264', '0.629', '-0.2218', '0.4788', '0.1819', '-0.4258', '0.1283', '-0.5605', '0.0325', '-0.7666', '0.3186', '0.571', '-0.4907', '0.1847', '-0.1103', '0.1054', '-0.0167', '-0.11163', '0.2986', '0.1545', '0.1871', '1.021', '-0.2227', '-0.1587', '-0.261', '0.377', '0.2268', '-0.0944', '0.5874', '0.3467', '0.293', '0.614', '0.1227', '0.4585', '0.2908', '0.1416', '0.08673', '0.2234', '-0.3555', '-0.06177', '-0.2489', '-0.3513', '1.155', '0.3472', '-0.3157', '0.4634', '0.286', '0.8633', '-0.2751', '-0.0218', '0.4602', '-0.5605', '-0.2188', '0.003933']",,,C567709,,,,
mondo:0013178,congenital muscular dystrophy due to LMNA mutation,"['LMNA congenital muscular dystrophy', 'muscular dystrophy Congenital, LMNA-related', 'L-CMD', 'MDCL', 'muscular dystrophy, congenital, LMNA-related', 'congenital muscular dystrophy caused by mutation in LMNA', 'LMNA-related congenital muscular dystrophy', 'muscular dystrophy, congenital', 'congenital muscular dystrophy LMNA-related']",0110640,613205,157973,C2750785,"['-0.0802', '-0.85', '-0.8735', '-0.3452', '0.3955', '-0.9824', '0.6963', '1.066', '-1.521', '-0.8057', '-0.03638', '0.4578', '-0.1278', '0.9683', '0.0956', '0.5522', '-0.787', '-0.3071', '-0.152', '-0.869', '0.2384', '0.05054', '0.2673', '0.3213', '0.1825', '-0.262', '0.014915', '-0.275', '0.23', '-0.1027', '0.9614', '0.3914', '0.679', '-0.2169', '-0.005764', '-0.2207', '-0.09357', '0.1837', '0.1969', '-0.282', '0.0463', '-0.4612', '-0.2343', '0.5527', '-0.4092', '0.291', '-0.462', '0.4697', '-0.189', '0.1854', '0.1967', '-0.3472', '-0.3206', '-0.3867', '0.0729', '-0.2957', '0.3354', '0.4678', '-0.1022', '0.2198', '-0.01904', '0.257', '-0.2174', '0.11926', '-0.1833', '-0.0884', '-0.307', '0.846', '-0.409', '-0.293', '-0.281', '0.472', '0.0294', '-0.1388', '0.6475', '0.621', '-0.02808', '0.1624', '0.1293', '0.2993', '0.5605', '-0.003424', '0.16', '0.04852', '-0.3967', '0.11786', '0.1422', '-0.09314', '0.805', '0.09076', '-0.2825', '-0.1307', '0.02402', '1.018', '-0.1841', '0.2173', '0.3489', '-0.4658', '-0.01764', '0.03857']",C148369,,C567708,,,,
mondo:0013179,hereditary spastic paraplegia 44,"['SPG44', 'autosomal recessive complex spastic paraplegia caused by mutation in GJC2', 'autosomal recessive spastic paraplegia 44', 'hereditary spastic paraplegia type 44', 'spastic paraplegia 44, autosomal recessive', 'autosomal recessive spastic paraplegia type 44', 'GJC2 autosomal recessive complex spastic paraplegia']",0110796,613206,320401,C2750784,"['-0.645', '-0.04236', '0.1328', '-0.7485', '-0.1509', '-0.6714', '-0.4407', '0.6846', '-0.882', '-0.1875', '-0.4592', '0.03793', '-0.3303', '-0.505', '0.4016', '-0.2107', '0.03854', '-0.804', '-0.03378', '-0.5176', '0.606', '-0.1558', '0.2466', '0.1367', '0.7007', '0.1151', '0.06226', '0.10144', '0.184', '0.08826', '-0.0966', '0.338', '-0.05606', '-0.3257', '0.010864', '-0.4617', '-0.1796', '0.04492', '-0.00248', '-0.2664', '0.687', '-0.845', '0.09924', '0.3994', '-0.4038', '-0.4165', '-0.3848', '0.12244', '0.721', '-0.2593', '0.3054', '0.06885', '-0.8135', '-0.1324', '-0.1818', '-0.3845', '0.703', '-0.727', '-0.608', '0.5522', '0.01932', '0.2046', '0.4097', '0.5283', '-0.815', '-0.4072', '0.309', '0.2612', '-0.088', '0.3303', '-0.4788', '0.683', '0.04706', '-0.1642', '0.4697', '0.3318', '0.2074', '0.3362', '-0.2715', '-0.1228', '0.0659', '-0.5107', '0.7314', '0.229', '-0.2961', '-0.3389', '-0.4512', '0.6123', '0.09015', '0.2144', '0.2057', '0.7773', '0.09784', '0.3079', '0.866', '0.506', '0.3447', '-0.6704', '0.3286', '0.4927']",,,C567707,,,,
mondo:0013180,"asthma-related traits, susceptibility to, 8","['Rhinoconjunctivitis, susceptibility to', 'asthma-related traits, susceptibility to, 8', 'ASRT8', 'asthma-RELATED traits, susceptibility to, 8']",,613207,,,,,,,,,,
mondo:0013181,amelogenesis imperfecta hypomaturation type 2A3,"['WDR72 amelogenesis imperfecta', 'amelogenesis imperfecta, type IIA3', 'amelogenesis imperfecta hypomaturation type IIA3', 'amelogenesis imperfecta caused by mutation in WDR72', 'amelogenesis imperfecta type IIA3', 'AI2A3', 'amelogenesis imperfecta, hypomaturation type, IIA3']",0110061,613211,,C2750771,,,,C567706,,,,
mondo:0013182,chromosome 17p13.3 duplication syndrome,"['chromosome 17p13.3 centromeric duplication syndrome', 'trisomy 17p13.3', 'chromosome 17p13.3, centromeric, DUPLICATION syndrome', 'dup(17)(p13.3)', '17p13.3 duplication syndrome', '17p13.3 microduplication syndrome']",0060432,613215,217385,C4304641,,,,C567705,,,,
mondo:0013183,congenital stationary night blindness 1C,"['congenital stationary night blindness type 1C', 'TRPM1 congenital stationary night blindness', 'congenital stationary night blindness 1C autosomal recessive', 'night blindness, congenital stationary (complete), 1C, autosomal recessive', 'congenital stationary night blindness caused by mutation in TRPM1', 'CSNB, complete, autosomal recessive', 'night blindness, congenital stationary, type 1C', 'CSNB1C']",0110867,613216,,C2750747,,,,C567704,,,,
mondo:0013184,congenital diarrhea 5 with tufting enteropathy,"['EPCAM secretory diarrhoea', 'congenital familial intractable diarrhoea with epithelial or epithelium abnormalities', 'congenital familial intractable diarrhoea with enterocytes assembly abnormalities', 'tufting enteropathy', 'IED', 'congenital enteropathy', 'DIAR5', 'secretory diarrhea caused by mutation in EPCAM', 'enteropathy, congenital tufting', 'congenital familial intractable diarrhea with enterocytes assembly abnormalities', 'congenital familial intractable diarrhea with epithelial or epithelium abnormalities', 'diarrhoea 5, with tufting enteropathy, congenital', 'EPCAM secretory diarrhea', 'intestinal epithelial dysplasia', 'intestinal epithelial cell dysplasia', 'congenital tufting enteropathy', 'secretory diarrhoea caused by mutation in EPCAM', 'diarrhea 5, with tufting enteropathy, congenital']",0060776,613217,92050,C4275062,"['0.4133', '0.359', '0.549', '0.4243', '-0.3948', '-0.783', '-0.82', '0.5454', '-0.0831', '-0.2266', '0.602', '0.4375', '0.3193', '0.525', '-0.9985', '0.2852', '-0.4734', '0.2153', '-0.563', '-0.931', '-0.0851', '-0.09564', '-0.1471', '0.02374', '0.1644', '-0.3914', '-0.699', '0.5454', '0.462', '-1.06', '-0.033', '-0.572', '-0.003332', '0.2913', '1.078', '0.571', '-0.2778', '0.1451', '0.35', '0.2384', '-0.595', '-0.338', '-0.314', '-0.6973', '0.385', '0.2341', '-0.2455', '-0.04837', '-0.3767', '1.045', '-0.8394', '-0.328', '0.3262', '-0.673', '0.00415', '-0.1792', '-0.3157', '-0.02776', '-0.6016', '-0.1158', '0.613', '0.4607', '0.2339', '-0.63', '0.0558', '-0.1627', '0.3923', '-0.1875', '0.2778', '0.7905', '-0.2898', '0.6406', '0.257', '-0.657', '0.6655', '0.25', '-0.2185', '-0.001953', '0.0629', '0.6157', '-0.10425', '-0.605', '0.006638', '0.1199', '0.11053', '0.503', '0.4612', '0.1581', '-0.006245', '-0.2374', '-0.3672', '-0.3306', '-0.4282', '-0.353', '0.609', '0.4658', '0.4326', '-1.31', '-0.002249', '-0.1697']",,,C567703,,,,
mondo:0013185,"leprosy, susceptibility to, 5","['leprosy caused by mutation in TLR1', 'leprosy, protection against', 'leprosy, susceptibility to, 5', 'LPRS5', 'susceptibility to leprosy 5', 'leprosy, susceptibility to, type 5', 'TLR1 leprosy']",,613223,,,,,,,,,,
mondo:0013186,Noonan syndrome 6,"['NS6', 'NRAS gene related Noonan syndrome', 'NRAS Noonan syndrome', 'Noonan syndrome caused by mutation in NRAS', 'Noonan syndrome 6', 'Noonan syndrome type 6']",0060584,613224,,C2750732,,C176934,,C548084,,,,
mondo:0013187,"factor XIII, A subunit, deficiency of","['factor XIII, A subunit, deficiency of', 'factor XIIIA deficiency']",,613225,,C2584877,,,,C567691,,,,
mondo:0013188,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3","['cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 3', 'cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 3', 'CA8 dysequilibrium syndrome', 'dysequilibrium syndrome caused by mutation in CA8', 'cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3', 'CAMRQ3', 'cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 3', 'cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3', 'cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 3']",,613227,,C2750509,,,,C567690,,,,
mondo:0013189,trichotillomania,"['TTM', 'trichotillomania', 'trichotillomania, multifactorial']",0050587,613229,,,,C94336,,D014256,312.39,F63.3,,
mondo:0013190,"factor XIII, b subunit, deficiency of","['factor XIII, b subunit, deficiency of', 'factor XIIIB deficiency']",,613235,,,,,,C567688,,,,
mondo:0013191,focal segmental glomerulosclerosis 5,"['glomerulosclerosis, focal segmental, 5', 'focal segmental glomerulosclerosis type 5', 'INF2 focal segmental glomerulosclerosis', 'focal segmental glomerulosclerosis 5', 'focal segmental glomerulosclerosis caused by mutation in INF2', 'FSGS5']",0111130,613237,,C2750475,,,,C567687,,,,
mondo:0013192,"spondyloarthropathy, susceptibility to, 3","['SPDA3', 'spondyloarthropathy, susceptibility to, 3']",0080605,613238,,,,,,,,,,
mondo:0013193,"thyrotoxic periodic paralysis, susceptibility to, 2","['thyrotoxic periodic paralysis caused by mutation in KCNJ18', 'TTPP2', 'KCNJ18 thyrotoxic periodic paralysis', 'thyrotoxic periodic paralysis, susceptibility to, type 2', 'thyrotoxic periodic paralysis, susceptibility to, 2']",,613239,,,,,,,,,,
mondo:0013194,Pseudopili annulati,['Pseudopili annulati'],,613241,,,,,,,,,,
mondo:0013195,hypertrophic cardiomyopathy 13,"['TNNC1 hypertrophic cardiomyopathy', 'cardiomyopathy familial hypertrophic 13', 'cardiomyopathy, familial hypertrophic, 13', 'hypertrophic cardiomyopathy type 13', 'cardiomyopathy, hypertrophic, 13', 'CMH13', 'cardiomyopathy, familial hypertrophic, type 13', 'hypertrophic cardiomyopathy caused by mutation in TNNC1']",0110319,613243,,C2750472,,,,C567686,,,,
mondo:0013196,Lynch syndrome 8,"['hereditary nonpolyposis colon cancer caused by mutation in EPCAM', 'colorectal cancer, hereditary nonpolyposis, type 8', 'HNPCC8', 'EPCAM hereditary nonpolyposis colon cancer']",0070270,613244,,C2750471,,,,C567685,,,,
mondo:0013197,hypertrophic cardiomyopathy 14,"['hypertrophic cardiomyopathy caused by mutation in MYH6', 'cardiomyopathy, hypertrophic, 14', 'cardiomyopathy familial hypertrophic 14', 'cardiomyopathy, familial hypertrophic, 14', 'cardiomyopathy, familial hypertrophic, type 14', 'CMH14', 'hypertrophic cardiomyopathy type 14', 'MYH6 hypertrophic cardiomyopathy']",0110320,613251,,C2750467,,,,C567684,,,,
mondo:0013198,dilated cardiomyopathy 1EE,"['familial isolated dilated cardiomyopathy caused by mutation in MYH6', 'CMD1EE', 'cardiomyopathy, dilated, type 1Ee', 'dilated cardiomyopathy type 1EE', 'MYH6 familial isolated dilated cardiomyopathy', 'cardiomyopathy, dilated, 1EE']",0110453,613252,,C2750466,,,,C567683,,,,
mondo:0013199,tuberous sclerosis 2,"['tuberous sclerosis, type 2', 'TSC2', 'tuberous sclerosis-2', 'tuberous sclerosis type 2', 'tuberous sclerosis 2', 'TSC2 Angiomyolipomas, renal, modifier of']",0080325,613254,,,,C75331,,C566021,,,,
mondo:0013200,hypertrophic cardiomyopathy 15,"['hypertrophic cardiomyopathy type 15', 'cardiomyopathy familial hypertrophic 15', 'cardiomyopathy, familial hypertrophic, 15', 'cardiomyopathy, familial hypertrophic, type 15', 'cardiomyopathy, hypertrophic, 15', 'CMH15', 'VCL hypertrophic cardiomyopathy', 'hypertrophic cardiomyopathy caused by mutation in VCL']",0110321,613255,,C2750459,,,,C567681,,,,
mondo:0013201,Waardenburg syndrome type 4B,"['EDN3 Waardenburg syndrome', 'Waardenburg syndrome, type 4B, with Hirschsprung disease', 'WS4B', 'Waardenburg syndrome, type 4B', 'Waardenburg syndrome caused by mutation in EDN3', 'Waardenburg syndrome type IVB', 'Waardenburg syndrome with Hirschsprung disease type 4B']",0110954,613265,,C2750457,,,,C567680,,,,
mondo:0013202,Waardenburg syndrome type 4C,"['WS4C', 'Waardenburg syndrome type IVC', 'Waardenburg syndrome with Hirschsprung disease type 4C', 'Waardenburg syndrome, type 4C', 'Waardenburg syndrome with Hirschsprung disease, type 4C']",0110955,613266,,C2750452,,,,C567679,,,,
mondo:0013203,"corneal dystrophy, Fuchs endothelial, 3","['Fcd2 locus', 'FECD3', 'corneal dystrophy, Fuchs endothelial, type 3', 'corneal dystrophy, Fuchs endothelial, 3', 'TCF4 Fuchs^ endothelial dystrophy', 'corneal dystrophy, Fuchs endothelial, late-onset', 'Fuchs^ endothelial dystrophy caused by mutation in TCF4']",,613267,,C2750451,,,,C567678,,,,
mondo:0013204,"corneal dystrophy, Fuchs endothelial, 4","['corneal dystrophy, Fuchs endothelial, type 4', 'corneal dystrophy, Fuchs endothelial, 4', 'corneal dystrophy, Fuchs endothelial, late-onset', 'FECD4', 'Fuchs^ endothelial dystrophy caused by mutation in SLC4A11', 'SLC4A11 Fuchs^ endothelial dystrophy']",,613268,,C2750450,,,,C567677,,,,
mondo:0013205,"corneal dystrophy, fuchs endothelial, 5","['corneal dystrophy, Fuchs endothelial, 5', 'Fcd3 locus', 'corneal dystrophy, Fuchs endothelial, late-onset', 'FECD5']",,613269,,C2750449,,,,C567676,,,,
mondo:0013206,"corneal dystrophy, Fuchs endothelial, 6","['Fuchs^ endothelial dystrophy caused by mutation in ZEB1', 'FECD6', 'corneal dystrophy, Fuchs endothelial, late-onset', 'corneal dystrophy, Fuchs endothelial, 6', 'corneal dystrophy, Fuchs endothelial, type 6', 'ZEB1 Fuchs^ endothelial dystrophy']",,613270,,C2750448,,,,C567675,,,,
mondo:0013207,"corneal dystrophy, fuchs endothelial, 7","['Fcd4 locus', 'corneal dystrophy, Fuchs endothelial, 7', 'FECD7', 'corneal dystrophy, Fuchs endothelial, late-onset']",,613271,,C2750447,,,,C567674,,,,
mondo:0013208,cirrhosis - dystonia - polycythemia - hypermanganesemia syndrome,"['hypermanganesemia with dystonia 1', 'HMDPC', 'hypermanganesemia with dystonia, polycythemia, and cirrhosis', 'hypermanganesemia with dystonia polycythemia and cirrhosis', 'HMNDYT1']",0080536,613280,309854,CN035550,"['0.00808', '0.2957', '0.6406', '-0.3005', '-0.4238', '-0.2361', '-0.4102', '0.0494', '-0.02533', '0.2025', '0.3882', '-0.2852', '-0.1304', '-0.01625', '-0.3816', '-0.9106', '0.0743', '0.2212', '-0.0825', '-0.4685', '-0.3933', '-0.188', '0.0967', '0.1365', '-0.2242', '-0.05588', '0.0956', '0.4998', '-0.287', '-0.218', '0.6636', '-0.661', '0.285', '-0.3054', '0.05902', '0.0689', '-0.644', '0.328', '0.2128', '-0.4817', '0.0775', '0.12415', '-0.1272', '0.4485', '0.0545', '-0.01475', '0.2451', '-0.5366', '0.4822', '-0.5464', '-0.1982', '0.2498', '0.1326', '0.0696', '-0.384', '0.05734', '-0.08', '-0.2454', '-0.7856', '-0.4727', '0.387', '0.0721', '0.2637', '-0.6343', '-0.5166', '0.0809', '-0.10175', '0.586', '-0.673', '0.5405', '-0.0981', '0.704', '-0.2192', '-0.4907', '0.3337', '0.1376', '0.3613', '0.6377', '0.5757', '0.1725', '-0.2239', '-0.1522', '-0.4312', '-0.1401', '-0.03397', '0.2369', '-0.10803', '-0.393', '1.056', '-0.607', '0.578', '0.781', '-0.5938', '0.558', '0.378', '0.61', '-0.4407', '-0.1273', '0.257', '-0.164']",,,C548016,277.89,,,
mondo:0013209,non-alcoholic fatty liver disease,"['fatty liver disease, nonalcoholic, susceptibility to, 1', 'NAFLD', 'liver disease, alcoholic, susceptibility to, 1', 'NAFLD - nonalcoholic fatty liver disease', 'NAFLD1', 'non-alcoholic fatty liver disease', 'nonalcoholic fatty liver disease', 'non-alcoholic fatty liver', 'fatty liver disease, nonalcoholic']",0080546,,33271,,"['0.2126', '-0.1696', '0.00912', '-0.2104', '0.465', '-0.1298', '-0.355', '-0.1119', '-0.304', '0.6797', '0.674', '0.1721', '-0.1318', '0.6245', '-0.7114', '-0.5728', '-0.01811', '0.002932', '-0.77', '-0.298', '-0.5728', '-0.276', '0.00814', '0.07776', '-0.227', '-0.76', '-0.29', '0.625', '-0.3228', '-0.6265', '0.242', '0.1345', '0.3447', '-0.1549', '0.4263', '-0.2242', '-1.443', '-0.06616', '0.633', '-0.3574', '-0.3171', '-0.09326', '0.2043', '-0.4102', '-0.0285', '-0.328', '0.3237', '-0.299', '0.07886', '0.1454', '-0.1042', '-0.1903', '0.4614', '0.2039', '-0.1824', '-0.3772', '-0.002985', '0.4104', '-0.688', '-0.5977', '0.2673', '0.416', '0.108', '0.0201', '0.1398', '0.3953', '0.4014', '0.382', '-0.2913', '-0.06244', '-0.04346', '0.3066', '0.3027', '-0.879', '0.7505', '0.5195', '0.41', '0.397', '0.001891', '0.512', '-0.3735', '-0.415', '-0.6255', '-0.414', '0.4492', '0.03607', '0.2502', '-0.3125', '0.58', '0.2343', '0.6636', '0.1467', '-0.3389', '0.445', '0.711', '-0.04935', '-0.7354', '-0.6304', '-0.3445', '-0.0154']",C84444,1001248,D065626,571.8,,10029530,
mondo:0013210,autosomal recessive nonsyndromic hearing loss 25,"['DFNB25', 'deafness, autosomal recessive type 25', 'GRXCR1 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness 25', 'autosomal recessive nonsyndromic deafness type 25', 'autosomal recessive deafness 25', 'deafness, autosomal recessive 25', 'autosomal recessive nonsyndromic deafness caused by mutation in GRXCR1']",0110483,613285,,C1414017,,,,,,,,
mondo:0013211,dilated cardiomyopathy 1FF,"['CMD1FF', 'cardiomyopathy, dilated, 1FF', 'cardiomyopathy, dilated, type 1Ff', 'dilated cardiomyopathy type 1FF']",0110459,613286,,C2750091,,,,C567654,,,,
mondo:0013212,Charcot-Marie-Tooth disease axonal type 2N,"['Charcot-Marie-Tooth neuropathy axonal type 2N', 'Charcot-Marie-Tooth disease type 2 caused by mutation in AARS', 'Charcot-Marie-Tooth disease type 2N', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2N', 'autosomal dominant Charcot-Marie-Tooth disease type 2N', 'Charcot-Marie-Tooth neuropathy, axonal, type 2N', 'Charcot-Marie-Tooth disease, axonal, type 2N', 'AARS Charcot-Marie-Tooth disease type 2', 'CMT2N', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2N']",0110177,613287,228174,C4304671,"['0.3684', '0.304', '0.1713', '-0.3696', '0.1342', '-0.4226', '-0.0391', '0.5947', '-0.7363', '-0.2944', '-0.239', '0.4583', '-0.414', '0.4768', '-0.1938', '0.0535', '-0.07916', '-0.5854', '-0.5713', '-0.685', '0.11273', '0.4956', '0.2544', '0.6235', '0.3843', '0.2734', '0.3044', '0.2476', '0.1389', '-0.00695', '-0.03665', '-0.669', '-0.01941', '0.1283', '0.1888', '-0.8423', '-0.433', '-0.2969', '0.591', '-0.24', '-1.401', '-0.5386', '-0.2856', '0.2888', '-0.2412', '-0.1809', '0.1829', '-0.1499', '0.0338', '-0.292', '0.1521', '0.2644', '-0.05603', '-1.082', '0.1431', '-0.2186', '0.1582', '0.3506', '-0.9233', '-0.4456', '-0.2883', '-0.004356', '0.7417', '0.426', '-0.8066', '0.8735', '-0.1604', '0.457', '-0.592', '0.2119', '-0.6714', '-0.15', '0.014175', '-0.4604', '1.3', '0.742', '-0.2235', '0.4985', '0.0756', '-0.492', '-0.2483', '-0.322', '0.857', '0.4944', '-0.0724', '0.0497', '-0.05862', '0.8325', '0.758', '0.6646', '0.1234', '-0.1725', '0.08777', '0.5723', '0.3376', '0.744', '0.7114', '-0.5005', '-0.08105', '0.4348']",,,C567653,,,,
mondo:0013213,"hearing loss, cisplatin-induced, susceptibility to","['CIHL', 'hearing loss, cisplatin-induced, susceptibility to']",,613290,,,,,,,,,,
mondo:0013214,"bile acid malabsorption, primary, 1","['bile acid malabsorption, primary', 'Bile acid malabsorption, primary, 1', 'PBAM']",,613291,449262,C2750087,,,,C567652,,,,
mondo:0013215,autosomal recessive nonsyndromic hearing loss 79,"['autosomal recessive nonsyndromic deafness type 79', 'deafness, autosomal recessive type 79', 'autosomal recessive deafness 79', 'deafness, autosomal recessive 79', 'autosomal recessive nonsyndromic deafness caused by mutation in TPRN', 'autosomal recessive nonsyndromic deafness 79', 'TPRN autosomal recessive nonsyndromic deafness', 'DFNB79']",0110526,613307,,C2750082,,,,C567651,,,,
mondo:0013216,Diamond-Blackfan anemia 9,"['Diamond-Blackfan anemia caused by mutation in RPS10', 'RPS10 Diamond-Blackfan anaemia', 'Diamond-Blackfan Anemia type 9', 'Diamond-Blackfan anemia 9', 'Diamond-Blackfan anaemia caused by mutation in RPS10', 'DBA9', 'RPS10 Diamond-Blackfan anemia', 'Diamond-Blackfan Anaemia type 9']",0111884,613308,,C2750081,,C176918,,C567650,,,,
mondo:0013217,Diamond-Blackfan anemia 10,"['RPS26 Diamond-Blackfan anaemia', 'RPS26 Diamond-Blackfan anemia', 'Diamond-Blackfan Anemia type 10', 'DBA10', 'Diamond-Blackfan anemia caused by mutation in RPS26', 'Diamond-Blackfan anemia 10', 'Diamond-Blackfan anaemia caused by mutation in RPS26', 'Diamond-Blackfan Anaemia type 10']",0111888,613309,,C2750080,,C176919,,C567649,,,,
mondo:0013218,exudative vitreoretinopathy 5,"['TSPAN12 exudative vitreoretinopathy', 'exudative vitreoretinopathy 5', 'EVR5', 'exudative vitreoretinopathy type 5', 'exudative vitreoretinopathy caused by mutation in TSPAN12']",0111408,613310,,C2750079,,,,C567648,,,,
mondo:0013219,"hypophosphatemic rickets, autosomal recessive, 2","['hypophosphatemic rickets, autosomal recessive, 2', 'hypophosphatemic rickets, autosomal recessive, type 2', 'ARHR2', 'autosomal recessive hypophosphatemic rickets caused by mutation in ENPP1', 'ENPP1 autosomal recessive hypophosphatemic rickets']",,613312,,C2750078,,,,C567647,,,,
mondo:0013220,hemochromatosis type 2B,"['HFE2B', 'hemochromatosis, type 2B', 'HAMP hemochromatosis type 2', 'hemochromatosis type 2 caused by mutation in HAMP']",0111032,613313,,C1865616,,,,C566557,,,,
mondo:0013221,Miyoshi muscular dystrophy 2,"['Miyoshi muscular dystrophy 2', 'MIYOSHI muscular dystrophy 2', 'Miyoshi myopathy 2', 'MMD2']",0070200,613318,,C2750077,,,,C567646,,,,
mondo:0013222,Miyoshi muscular dystrophy 3,"['MMD3', 'distal anoctaminopathy', 'Miyoshi myopathy 3', 'Miyoshi muscular dystrophy type 3', 'Miyoshi muscular dystrophy 3']",0070201,613319,399096,C2750076,"['-0.2769', '-0.6494', '-0.804', '0.1753', '0.4983', '-0.833', '0.2133', '1.188', '-1.423', '-0.939', '-0.03467', '0.3657', '-0.3787', '0.798', '0.2915', '0.3352', '-0.7954', '-0.491', '-0.07355', '-0.7324', '0.071', '-0.1766', '0.05164', '0.4197', '0.1163', '-0.05823', '-0.1445', '-0.7974', '-0.05295', '-0.2471', '0.8457', '0.1405', '0.3997', '-0.03174', '0.0534', '-0.2119', '-0.7163', '0.2009', '0.1231', '-0.2441', '0.2374', '-0.693', '-0.1516', '0.512', '0.1087', '0.4995', '-0.08057', '0.302', '-0.2568', '0.6514', '0.1818', '-0.2937', '0.253', '-0.7603', '0.08606', '-0.3308', '0.3276', '0.4863', '-0.07495', '-0.1265', '0.1399', '0.073', '-0.1885', '-0.05844', '-0.10565', '0.273', '-0.01927', '0.5005', '-0.26', '-0.04358', '-0.3003', '-0.0213', '0.1306', '0.2068', '0.9043', '0.555', '-0.408', '0.1926', '0.255', '0.1853', '0.2546', '-0.1942', '0.1821', '0.1461', '-0.08356', '0.6113', '-0.3906', '-0.2878', '0.6816', '0.0377', '-0.246', '-0.0917', '0.03198', '0.9214', '0.2546', '-0.0404', '0.327', '-0.2861', '-0.0819', '-0.0995']",,,C567645,,,,
mondo:0013223,"autosomal recessive spondylometaphyseal dysplasia, Megarbane type","['spondylometaphyseal dysplasia, Megarbane-Dagher-Melike type', 'autosomal recessive spondylometaphyseal dysplasia, Mégarbané type', 'spondylometaphyseal dysplasia, MEGARBANE-DAGHER-MELKI type', 'chondrodysplasia, Megarbane-Dagher-Melki type', 'PAM16 spondylodysplastic dysplasia', 'SMDMDM']",0112304,613320,401979,C2750075,"['-0.5366', '0.2004', '0.3796', '-0.4758', '0.3818', '-0.3457', '-0.1026', '0.5615', '-0.5317', '-0.393', '-0.1656', '0.07446', '0.0825', '-0.1302', '0.2244', '0.268', '0.3833', '0.0464', '-0.511', '-0.534', '0.04874', '0.1909', '0.1929', '-0.2477', '0.2021', '-0.002111', '-0.07733', '-0.115', '0.239', '-0.0772', '0.2281', '-0.2284', '0.2664', '0.1542', '0.359', '-0.0661', '-0.05518', '-0.3232', '0.01787', '-0.1454', '0.1247', '-0.3218', '0.002804', '0.04962', '-0.2198', '-0.3735', '-0.08276', '0.365', '0.06616', '-0.329', '0.2041', '-0.0518', '-0.09814', '0.3152', '-0.276', '-0.6763', '-0.1588', '-0.11945', '-0.04733', '0.3418', '0.2642', '-0.005444', '-0.3352', '-0.083', '-0.03165', '-0.2124', '0.1458', '0.4282', '-0.258', '0.3235', '-0.3132', '0.144', '0.2703', '-0.3936', '-0.1087', '0.03973', '-0.2356', '-0.06113', '-0.252', '0.0812', '0.00664', '0.2097', '0.01724', '0.2178', '-0.261', '0.181', '0.01059', '0.3552', '0.2783', '0.1781', '-0.0939', '0.03305', '9.93e-05', '0.03513', '0.7197', '0.356', '0.505', '-0.3696', '0.581', '-0.02063']",,,C567644,,,,
mondo:0013224,rhabdoid tumor predisposition syndrome 2,"['SMARCA4 familial rhabdoid tumor', 'SMARCA4 familial rhabdoid tumour', 'familial rhabdoid tumor caused by mutation in SMARCA4', 'familial rhabdoid tumour caused by mutation in SMARCA4', 'RTPS2', 'rhabdoid tumor predisposition syndrome type 2', 'rhabdoid tumor predisposition syndrome 2', 'rhabdoid tumour predisposition syndrome type 2']",,613325,,C2750074,,C178394,,C567643,,,,
mondo:0013225,congenital generalized lipodystrophy type 4,"['congenital generalised lipodystrophy (disease) caused by mutation in CAVIN1', 'Berardinelli-Seip congenital lipodystrophy, type 4, with muscular dystrophy', 'Berardinelli-Seip congenital lipodystrophy type 4 with muscular dystrophy', 'lipodystrophy, Berardinelli-Seip congenital, type 4, with muscular dystrophy', 'generalized congenital lipodystrophy with myopathy', 'BSCL4', 'GCL4', 'CAVIN1 congenital generalized lipodystrophy (disease)', 'CGL4', 'lipodystrophy, congenital generalized, type 4', 'generalised congenital lipodystrophy type 4', 'CAVIN1 congenital generalised lipodystrophy (disease)', 'generalized congenital lipodystrophy type 4', 'generalised congenital lipodystrophy with myopathy']",0111138,613327,228429,C2750069,"['-0.1893', '0.1459', '0.04752', '-0.03204', '0.0884', '-0.3372', '0.0489', '0.1941', '-0.296', '-0.1254', '-0.1405', '-0.04913', '-0.0712', '0.0596', '-0.02635', '0.002289', '0.02924', '-0.0699', '-0.1594', '-0.3655', '0.11395', '-0.04654', '0.1818', '0.0384', '0.09515', '0.02719', '0.02284', '-0.04462', '-0.0303', '-0.09973', '0.1895', '0.02234', '0.2189', '0.0843', '0.1062', '-0.05295', '-0.03387', '-0.1012', '-0.05402', '-0.1184', '0.0002192', '-0.2683', '-0.01234', '0.1794', '0.01205', '-0.1487', '-0.05243', '0.1763', '0.1449', '0.02728', '-0.0606', '-0.01026', '0.267', '-0.02087', '-0.1656', '-0.1763', '0.2458', '-0.02611', '-0.2103', '-0.0726', '0.1549', '0.04486', '0.1626', '-0.000961', '-0.01837', '0.1718', '0.17', '0.05902', '-0.1626', '0.1266', '-0.2161', '-0.04932', '0.1558', '-0.1002', '0.1409', '-0.02528', '0.1098', '-0.0083', '-0.08026', '-0.02325', '-0.03552', '0.00956', '-0.002394', '0.0749', '0.00433', '-0.11115', '0.11975', '0.3347', '0.2065', '0.154', '0.1818', '0.09717', '0.02666', '0.005154', '0.3384', '0.0763', '0.3608', '-0.2588', '-0.02992', '-0.02396']",,,C567642,,,,
mondo:0013226,combined immunodeficiency with faciooculoskeletal anomalies,"['ROIFMAN-Chitayat syndrome', 'Roifman-Chitayat syndrome, digenic', 'Roifman-Chitayat syndrome', 'combined immunodeficiency, Facial Dysmorphism, optic nerve atrophy, skeletal anomalies, and developmental delay']",,613328,221139,C2750068,,,,C567641,,,,
mondo:0013227,congenital plasminogen activator inhibitor type 1 deficiency,"['plasminogen activator inhibitor type 1 deficiency', 'congenital PAI-1 deficiency', 'plasminogen activator INHIBITOR-1 deficiency', 'hyperfibrinolysis due to Pai1 deficiency']",,613329,465,,"['-0.1487', '-0.5767', '-0.6226', '-0.3567', '0.064', '0.02486', '-0.2964', '0.06247', '-0.1354', '-0.0814', '-0.06836', '0.5664', '0.2188', '-0.2253', '0.0003526', '0.1615', '-0.0938', '-0.16', '-0.2253', '-0.4465', '-0.5156', '-0.12396', '0.4746', '-0.1207', '-0.4043', '0.01967', '0.1709', '0.3975', '0.3533', '-0.1665', '0.4004', '0.06744', '0.4817', '0.543', '-0.2954', '-0.1897', '0.004745', '-0.5244', '-0.01266', '0.09326', '0.09906', '0.0839', '0.559', '-0.1558', '0.2854', '0.3635', '-0.1732', '0.1658', '0.422', '-0.1517', '0.3376', '-0.4119', '0.125', '0.4187', '-0.3442', '-0.2471', '0.4324', '-0.2842', '-0.6445', '-0.309', '-0.2778', '0.3345', '0.3108', '-0.4019', '0.6504', '0.4995', '0.1552', '-0.388', '-0.825', '0.6646', '-0.3804', '-0.1017', '-0.03677', '-0.4902', '0.643', '1.044', '0.661', '-0.03503', '-0.0762', '-0.255', '-0.2324', '-0.1509', '0.0164', '0.0593', '0.343', '0.807', '0.2059', '0.3572', '0.579', '-0.3484', '0.4033', '0.6953', '0.2266', '-0.2893', '0.3323', '0.1565', '0.5947', '-0.41', '-0.0383', '-0.03238']",C133884,,C567640,,,,
mondo:0013228,spondylo-megaepiphyseal-metaphyseal dysplasia,"['spondylo-megaepiphyseal-metaphyseal dysplasia', 'SMMD']",,613330,228387,C2750066,"['-0.9478', '0.2026', '0.336', '-0.2489', '0.4712', '-0.1938', '-0.1471', '0.5596', '-0.59', '-0.2289', '0.01779', '0.2175', '-0.010124', '0.0806', '-0.0647', '0.2268', '0.445', '-0.3843', '-0.6055', '-0.6475', '0.08594', '-0.05942', '0.586', '-0.05908', '0.2761', '0.1539', '-0.015495', '0.2214', '-0.004208', '0.2043', '0.4778', '-0.397', '0.0749', '0.0662', '0.2156', '-0.4688', '-0.1515', '-0.3552', '0.03084', '-0.2399', '-0.1353', '-0.251', '0.0795', '0.03455', '0.007217', '-0.412', '-0.1923', '0.3699', '0.4197', '-0.1067', '-0.03226', '0.03418', '0.1306', '0.3606', '-0.3362', '-0.53', '-0.2369', '-0.1346', '0.0974', '-0.009865', '0.4963', '0.04456', '-0.6206', '-0.2761', '-0.1858', '0.1782', '0.0669', '0.622', '-0.4211', '0.2524', '-0.4636', '-0.1404', '0.245', '-0.1714', '-0.4197', '0.2004', '-0.232', '0.4045', '-0.01976', '-0.263', '0.01715', '0.03069', '0.333', '0.03708', '-0.1214', '0.0867', '-0.4216', '0.2388', '0.644', '0.2786', '-0.383', '0.01662', '-0.3271', '0.08954', '0.395', '0.3704', '0.6685', '-0.348', '0.6797', '0.2397']",,,C567639,,,,
mondo:0013229,hot water reflex epilepsy,"['epilepsy, hot water', 'water immersion epilepsy', 'hot water epilepsy', 'bathing epilepsy']",0081104,,166412,CN200053,,,,,345.10,,,
mondo:0013230,"epilepsy, hot water, 2","['HWE2', 'epilepsy, hot water, 2']",0081107,613340,,C3150536,,,,,,,,
mondo:0013231,Leber congenital amaurosis 14,"['retinitis pigmentosa, juvenile, LRAT-related', 'retinal dystrophy, early-onset Severe, LRAT-related', 'LRAT Leber congenital amaurosis', 'Leber congenital amaurosis type 14', 'retinitis pigmentosa, juvenile', 'retinal dystrophy, early-onset severe', 'LCA14', 'Leber congenital amaurosis 14', 'Leber congenital amaurosis caused by mutation in LRAT']",0110188,613341,791,C2750063,,,,C567636,,H35.5,,
mondo:0013232,"brachydactylous dwarfism, Mseleni type","['Mseleni JOINT disease', 'Mseleni joint disease', 'brachydactylous dwarfism Mseleni type', 'brachydactylous dwarfs of Mseleni']",,613342,2619,C2931420,,,,C537086,,,,
mondo:0013233,"spondyloepimetaphyseal dysplasia, Handigodu type","['spondyloepimetaphyseal dysplasia, Handigodu type', 'Hjd', 'Handigodu JOINT disease']",,613343,99642,C3150545,,,,,,,,
mondo:0013234,"hypokalemic periodic paralysis, type 2","['HOKPP2', 'hypokalemic periodic paralysis, type 2']",,613345,,C2750061,,,,C567635,,,,
mondo:0013235,"pancreatic cancer, susceptibility to, 2","['BRCA2 familial pancreatic carcinoma', 'pancreatic cancer 2', 'susceptibility to pancreatic cancer 2', 'pancreatic cancer, susceptibility to, type 2', 'Pnca2', 'familial pancreatic carcinoma caused by mutation in BRCA2', 'pancreatic cancer, susceptibility to, 2']",,613347,,,,,,,,,,
mondo:0013236,"pancreatic cancer, susceptibility to, 3","['familial pancreatic carcinoma caused by mutation in PALB2', 'PALB2 familial pancreatic carcinoma', 'pancreatic cancer, susceptibility to, type 3', 'pancreatic cancer, susceptibility to, 3', 'susceptibility to pancreatic cancer 3', 'Pnca3']",,613348,,,,,,,,,,
mondo:0013237,"susceptibility to mononeuropathy of the median nerve, mild","['carpal tunnel syndrome, susceptibility to', 'mononeuropathy of the median nerve, mild', 'MNMN']",,613353,,C3150596,,,,,,,,
mondo:0013238,chromosome 17q23.1-q23.2 deletion syndrome,"['Del(17)(q23.1q23.2)', 'chromosome 17q23.1-q23.2 deletion syndrome', '17q23.1q23.2 microdeletion syndrome', 'monosomy 17q23.1q23.2', 'monosomy 17q23.1-q23.2', 'chromosome 17q23.1-q23.2 deletion syndrome, isolated cases', '17q23.1-q23.2 microdeletion syndrome']",0060405,613355,261279,C4304591,,,,,,,,
mondo:0013239,hereditary spastic paraplegia 41,"['hereditary spastic paraplegia type 41', 'SPG41', 'spastic paraplegia 41, autosomal dominant', 'autosomal dominant spastic paraplegia 41', 'autosomal dominant spastic paraplegia type 41']",0110793,613364,320355,CN203988,,,,,,,,
mondo:0013240,maturity-onset diabetes of the young type 10,"['MODY10', 'maturity-onset diabetes of the young, type 10', 'INS maturity-onset diabetes of the young (disease)']",0111108,613370,,C3150617,,,,,,,,
mondo:0013241,spinocerebellar ataxia type 30,"['spinocerebellar ataxia 30', 'spinocerebellar ataxia type 30', 'SCA30']",0050979,613371,211017,C4304845,,,,C575214,,,,
mondo:0013242,maturity-onset diabetes of the young type 11,"['MODY11', 'BLK maturity-onset diabetes of the young (disease)', 'maturity-onset diabetes of the young, type 11']",0111109,613375,,C3150618,,,,,,,,
mondo:0013243,"neuronopathy, distal hereditary motor, type 2C","['HMN2C', 'HSPB3 neuronopathy, distal hereditary motor', 'neuropathy, distal hereditary motor, type 2C', 'neuronopathy, distal hereditary motor caused by mutation in HSPB3', 'HMN 2C', 'neuronopathy, distal hereditary motor, type IIC']",0111209,613376,,C3150619,,,,,,,,
mondo:0013244,brachydactyly type E2,"['BDE2', 'PTHLH brachydactyly type E', 'brachydactyly type E caused by mutation in PTHLH', 'brachydactyly, type E2']",0110976,613382,,C3150644,,,,,,,,
mondo:0013245,syndromic multisystem autoimmune disease due to ITCH deficiency,"['syndromic multisystem autoimmune disease', 'ITCH E3 ubiquitin ligase deficiency', 'ADMFD', 'autoimmune disease, syndromic multisystem', 'autoimmune disease, multisystem, with facial dysmorphism']",,613385,228426,C3150649,"['-0.1945', '0.1937', '0.3044', '-0.3127', '0.1159', '-0.010635', '0.11865', '0.04547', '-0.3687', '0.02267', '0.314', '0.000995', '0.2133', '-0.4756', '-0.3416', '0.07135', '0.1625', '0.1321', '-0.2744', '-0.695', '0.1982', '-0.1526', '0.2396', '-0.3901', '0.1604', '-0.03366', '-0.1372', '-0.04285', '0.3228', '-0.2922', '0.1392', '0.1969', '0.5303', '0.1979', '0.2411', '-0.1875', '-0.335', '-0.0436', '-0.161', '-0.494', '-0.2878', '0.154', '0.1708', '-0.161', '-0.04224', '-0.3643', '0.3357', '0.2225', '-0.05807', '0.0746', '-0.441', '0.2168', '0.283', '0.2517', '-0.5156', '-0.2588', '-0.1044', '-0.2908', '-0.2893', '0.07', '0.2688', '0.06555', '-0.2408', '-0.09814', '0.3416', '-0.0643', '0.311', '0.391', '-0.479', '0.4895', '-0.3423', '0.02316', '0.1931', '-0.00994', '-0.511', '-0.02228', '0.4102', '-0.3008', '-0.2695', '0.02467', '0.04382', '-0.1769', '-0.401', '0.2532', '0.1516', '0.09216', '-0.0752', '0.08777', '0.4077', '0.2081', '0.26', '0.2178', '0.2542', '0.0323', '0.6074', '0.212', '0.12354', '0.04718', '0.4802', '0.311']",,,,,,,
mondo:0013246,"fatty liver disease, nonalcoholic, susceptibility to, 2","['NAFLD2', 'fatty liver disease, nonalcoholic, susceptibility to, 2']",,613387,,,,,,,,,,
mondo:0013247,Fanconi renotubular syndrome 2,"['Fanconi renotubular syndrome 2', 'Fanconi syndrome caused by mutation in SLC34A1', 'Fanconi renotubular syndrome type 2', 'FRTS2', 'SLC34A1 Fanconi syndrome']",0080758,613388,,C3150652,,,,,,,,
mondo:0013248,Fanconi anemia complementation group O,"['Fanconi anaemia complementation group type O', 'RAD51C Fanconi anemia', 'Fanconi anemia, complementation group O', 'Fanconi anemia caused by mutation in Rad51C', 'Fanconi anaemia caused by mutation in Rad51C', 'Fanconi anemia complementation group type O', 'FANCO', 'RAD51C Fanconi anaemia', 'Rad51C Fanconi anemia', 'Fanconi Anemia, complementation group type O', 'Rad51C Fanconi anaemia', 'Fanconi anaemia caused by mutation in RAD51C']",0111096,613390,,C3150653,,,,,,,,
mondo:0013249,autosomal recessive nonsyndromic hearing loss 84A,"['autosomal recessive nonsyndromic deafness 84A', 'deafness, autosomal recessive 84A', 'deafness, autosomal recessive 84A, with vestibular dysfunction', 'PTPRQ autosomal recessive nonsyndromic deafness', 'autosomal recessive deafness 84A', 'deafness, autosomal recessive 84', 'DFNB84A', 'deafness, autosomal recessive 84a', 'autosomal recessive nonsyndromic deafness caused by mutation in PTPRQ', 'autosomal recessive deafness 84A with vestibular dysfunction', 'autosomal recessive nonsyndromic deafness type 84A', 'deafness, autosomal recessive type 84A']",0110529,613391,,C3150654,,,,,,,,
mondo:0013250,autosomal recessive nonsyndromic hearing loss 85,"['autosomal recessive deafness 85', 'DFNB85', 'autosomal recessive nonsyndromic deafness type 85', 'deafness, autosomal recessive 85', 'autosomal recessive nonsyndromic deafness 85']",0110531,613392,,C3160740,,,,,,,,
mondo:0013251,Birbeck granule deficiency,"['Birbeck granules, absence of', 'Birbeck granule deficiency']",,613393,,C3150657,"['-0.02274', '0.02072', '0.00574', '-0.00966', '-0.0001793', '-0.01556', '0.00954', '0.010414', '-0.003393', '-0.010414', '-0.00793', '-0.00967', '0.01144', '-0.00953', '-0.0116', '-0.01151', '-0.001758', '-0.00961', '-0.0187', '-0.0383', '-0.00486', '-0.005135', '0.02936', '0.0001813', '0.01397', '-0.000493', '-0.00491', '-0.0128', '-0.004097', '-0.00536', '0.01929', '0.01011', '0.02911', '0.005524', '0.00183', '-0.001788', '-0.014496', '-0.008644', '-0.00201', '-0.01461', '-0.005196', '-0.0167', '0.010765', '0.005295', '-0.01388', '-0.02008', '-0.009636', '0.01767', '0.000604', '0.02379', '-0.010025', '-0.01564', '0.004055', '0.0099', '-0.006092', '-0.0149', '0.02136', '-0.01241', '-0.035', '0.0009036', '0.003426', '0.003544', '0.00236', '-0.006424', '-0.001529', '0.003496', '0.01678', '0.01627', '-0.02591', '0.02914', '-0.02547', '-0.002443', '0.004097', '-0.01336', '0.000763', '0.00913', '-0.0008626', '-0.0098', '-0.0169', '-0.0015', '0.000616', '-0.001669', '0.00389', '0.01088', '-0.00983', '0.001531', '0.01752', '0.01358', '0.02132', '-0.00446', '0.007866', '0.01107', '-0.001386', '-0.00534', '0.04343', '0.01359', '0.0172', '-0.03238', '-0.008125', '0.01534']",,,,,,,
mondo:0013252,Warsaw breakage syndrome,"['WABS', 'WARSAW breakage syndrome', 'Warsaw breakage syndrome']",0060535,613398,280558,C3150658,"['-0.4792', '0.159', '0.5513', '-0.716', '0.638', '-0.4678', '0.1167', '0.313', '-0.3748', '-0.2668', '0.2778', '0.2651', '0.3682', '-0.284', '-0.2007', '0.1364', '0.1622', '-0.05573', '-0.08606', '-0.03604', '0.3977', '-0.02025', '-0.0878', '0.04016', '0.2927', '0.01898', '-0.3362', '-0.007584', '0.2288', '-0.516', '0.2456', '-0.00398', '0.508', '0.1895', '0.1746', '-0.05377', '-0.589', '-0.3223', '-0.1133', '-0.4705', '0.2754', '0.04102', '0.1681', '0.01808', '-0.2428', '-0.464', '-0.04095', '0.0772', '0.1927', '-0.006298', '-0.4827', '-0.3574', '-0.2234', '0.3293', '-0.04413', '-0.4028', '0.09375', '0.14', '-0.3796', '0.2211', '-0.0312', '0.02563', '-0.3706', '0.2974', '0.0389', '-0.143', '0.2023', '0.1864', '-0.1754', '0.3547', '-0.5356', '-0.0844', '0.1497', '0.1594', '-0.1202', '-0.09375', '0.1394', '-0.02444', '-0.1296', '-0.04385', '0.1204', '0.356', '-0.1426', '0.06885', '-0.357', '-0.09735', '0.1354', '0.691', '0.29', '0.5654', '0.1887', '0.2686', '-0.003176', '-0.124', '0.517', '0.1121', '0.3347', '-0.4885', '0.376', '0.03317']",C164675,,,759.89,,,
mondo:0013253,"breast-ovarian cancer, familial, susceptibility to, 3","['breast-ovarian cancer, familial, susceptibility to, 3', 'breast-ovarian cancer, familial, susceptibility to, type 3', 'BROVCA3', 'RAD51C hereditary breast ovarian cancer syndrome', 'hereditary breast ovarian cancer syndrome caused by mutation in Rad51C', 'ovarian cancer, familial, susceptibility to, 3', 'susceptibility to familial breast-ovarian cancer 3', 'Rad51C hereditary breast ovarian cancer syndrome', 'breast cancer, familial, susceptibility to, 3']",,613399,,,,,,,,,,
mondo:0013254,"microcephaly, seizures, and developmental delay","['EIEE10', 'MCSZ', 'early infantile epileptic encephalopathy-10', 'microcephaly, seizures, and developmental delay', 'microcephaly - seizures - developmental delay', 'epileptic encephalopathy, early infantile, 10']",0080457,613402,228418,C3150667,"['0.1537', '0.435', '0.362', '0.01382', '0.3555', '-0.1761', '0.528', '0.588', '-1.07', '-0.2101', '0.0759', '0.1346', '0.2468', '0.8013', '0.62', '-0.2634', '0.6543', '0.5044', '-0.649', '-1.332', '-0.311', '-0.1439', '0.08734', '-0.1882', '0.4043', '0.02051', '0.0393', '0.2678', '0.3142', '-0.05923', '-0.2449', '-0.7114', '0.5244', '0.129', '-0.11554', '0.822', '-0.4585', '-0.1556', '0.1748', '-0.3857', '0.066', '0.4214', '-0.694', '-0.4072', '0.128', '-0.5107', '0.979', '0.2214', '0.2432', '-0.05948', '0.0679', '-0.6787', '-0.21', '-0.1964', '-0.09894', '0.2352', '-0.808', '0.657', '-0.4155', '0.2367', '0.0417', '0.48', '0.3887', '0.04715', '-0.3032', '0.2944', '0.5728', '-0.1081', '-1.397', '0.273', '-0.4885', '1.124', '0.3193', '-1.008', '-0.0639', '0.373', '0.166', '-0.1637', '-0.2522', '-0.0999', '-0.3743', '0.9893', '-0.1925', '0.356', '0.05914', '-0.442', '0.285', '-0.4546', '1.049', '0.777', '-0.1241', '0.155', '-0.3018', '0.283', '-0.25', '0.6494', '0.63', '-0.542', '0.4438', '-0.7437']",,,,,,,
mondo:0013255,"arthrogryposis, renal dysfunction, and cholestasis 2","['arthrogryposis, renal dysfunction, and cholestasis type 2', 'arthrogryposis, renal dysfunction, and cholestasis 2', 'VIPAS39 arthrogryposis-renal dysfunction-cholestasis syndrome', 'ARCS2', 'arthrogryposis-renal dysfunction-cholestasis syndrome caused by mutation in VIPAS39']",0111354,613404,,C3150672,,,,,,,,
mondo:0013256,chromosome 15q24 deletion syndrome,"['WITKOS', 'Del(15)(q24)', 'monosomy 15q24', '15q24 microdeletion syndrome', 'chromosome 15q24 deletion syndrome', 'Witteveen-Kolk syndrome', 'chromosome 15Q24 Duplication syndrome', '15q24 recurrent microdeletion syndrome']",0060395,613406,94065,CN237818,"['0.2996', '0.3884', '0.616', '-0.5913', '0.524', '-0.0953', '0.5176', '0.8486', '-0.7188', '-0.4229', '-0.0075', '0.1772', '0.4102', '-0.2072', '0.09674', '0.2408', '0.0656', '-0.1869', '-0.6396', '-0.4302', '0.08844', '0.356', '0.2421', '0.1726', '0.08276', '-0.2366', '-0.3274', '0.1694', '0.7515', '-0.7026', '0.558', '-0.4797', '0.2676', '-0.0795', '-0.11835', '7.75e-06', '-0.7773', '-0.4927', '-0.1617', '-0.2001', '0.3684', '0.02304', '0.5493', '-0.2979', '0.2461', '-0.3928', '-0.1725', '0.72', '-0.3108', '-0.2303', '-0.5127', '-0.1201', '-0.7256', '-0.0483', '-0.769', '0.0822', '0.4348', '-0.2522', '0.1247', '0.5137', '0.2954', '0.6064', '-0.532', '0.249', '0.1783', '0.3809', '0.02487', '-0.03705', '-0.4072', '0.3362', '0.3376', '0.6973', '-0.693', '0.1405', '0.001976', '-0.153', '0.2368', '-0.828', '-0.03342', '0.3064', '-0.00925', '-0.012245', '0.1394', '0.2834', '-0.1348', '0.3262', '-0.03848', '0.512', '0.214', '0.00754', '0.0723', '0.6606', '-0.517', '0.1588', '0.664', '0.11444', '0.257', '0.003632', '0.274', '0.1644']",,,C579849,,,,
mondo:0013257,"leprosy, susceptibility to, 6","['LPRS6', 'leprosy, susceptibility to, 6']",,613407,,,,,,,,,,
mondo:0013258,"autism, susceptibility to, 16","['autism, susceptibility to, 16', 'AUTS16', 'susceptibility to autism 16', 'autism susceptibility 16', 'autism, susceptibility to, type 16', 'autism with or without seizures']",,613410,,,,,,,,,,
mondo:0013259,Oguchi disease-2,"['Oguchi disease 2', 'GRK1 Oguchi disease', 'congenital stationary night blindness Oguchi type 2', 'CSNBO2', 'night blindness, congenital stationary, Oguchi type 2', 'Oguchi disease caused by mutation in GRK1', 'Oguchi disease type 2']",0110713,613411,,C3150678,,,,,,,,
mondo:0013260,"esophagitis, eosinophilic, 2","['EOE2', 'esophagitis, eosinophilic, 2']",,613412,,C3150679,,,,,,,,
mondo:0013261,dilated cardiomyopathy 1R,"['dilated cardiomyopathy type 1R', 'cardiomyopathy, dilated, 1R', 'left ventricular noncompaction 4', 'ACTC1 familial isolated dilated cardiomyopathy', 'cardiomyopathy, dilated, type 1R', 'familial isolated dilated cardiomyopathy caused by mutation in ACTC1', 'CMD1R']",0110456,613424,,,,,,,,,,
mondo:0013262,dilated cardiomyopathy 1S,"['dilated cardiomyopathy-1S', 'MYH7 familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 1S', 'left ventricular noncompaction 5', 'familial isolated dilated cardiomyopathy caused by mutation in MYH7', 'cardiomyopathy, dilated, 1S', 'CMD1S', 'cardiomyopathy, dilated, type 1S']",0110454,613426,,,,,,C563538,,,,
mondo:0013263,retinitis pigmentosa 54,"['PCARE retinitis pigmentosa', 'retinitis pigmentosa type 54', 'retinitis pigmentosa caused by mutation in PCARE', 'retinitis pigmentosa 54', 'RP54']",0110364,613428,,C3150691,,,,,,H35.5,,
mondo:0013264,amyotrophic lateral sclerosis type 12,"['amyotrophic lateral sclerosis 12', 'amyotrophic lateral sclerosis caused by mutation in OPTN', 'OPTN amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis type 12', 'ALS12', 'amyotrophic lateral sclerosis 12 with or without frontotemporal dementia']",0060203,613435,,C3150692,,,,,,,,
mondo:0013265,"autism, susceptibility to, 17","['autism, susceptibility to, type 17', 'autism, susceptibility to, 17', 'autism susceptibility 17', 'susceptibility to autism 17', 'AUTS17']",,613436,,,,,,,,,,
mondo:0013266,"intellectual disability, autosomal dominant 20","['chromosome 5q14.3 deletion syndrome', 'neurodevelopmental disorder with hypotonia, stereotypic hand movements, and impaired language', 'intellectual disability, autosomal dominant 20', 'autosomal dominant non-syndromic intellectual disability caused by mutation in MEF2C', 'chromosome 5Q14.3 deletion syndrome, proximal', 'mental retardation, autosomal dominant 20', 'MEF2C autosomal dominant non-syndromic intellectual disability', 'intellectual disability, autosomal dominant type 20', 'mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations', 'MRD20', 'autosomal dominant intellectual disability 20', 'mental retardation, autosomal dominant type 20', 'autosomal dominant mental retardation 20', 'intellectual disability, stereotypic movements, epilepsy, and/or cerebral malformations']",0070050,613443,228384,C3150700,"['0.1131', '0.376', '0.1224', '-0.3357', '-0.3787', '-0.4246', '-0.08124', '0.8433', '-0.6436', '-0.7197', '-0.1617', '-0.4463', '0.1299', '-0.4644', '0.3323', '0.4548', '0.1439', '-0.159', '-0.4094', '-0.3672', '0.205', '-0.2397', '0.631', '-0.4539', '0.6187', '-0.4307', '-0.5474', '0.6904', '0.1231', '0.006863', '0.253', '-0.2091', '0.4932', '0.577', '0.209', '0.1835', '-0.10394', '0.02821', '0.10675', '-0.2085', '0.7656', '-0.4216', '-0.3745', '-0.431', '0.0952', '-0.4805', '0.1282', '0.175', '-0.04214', '-0.2637', '-0.05768', '0.2242', '-0.878', '0.3928', '-0.2386', '0.0639', '-0.0212', '-0.306', '0.1688', '-0.056', '-0.3838', '0.06866', '-0.02118', '0.3953', '-0.5117', '-0.2056', '0.528', '0.2966', '-0.2047', '0.6963', '-0.01753', '0.4106', '-0.425', '0.3127', '-0.482', '0.8877', '0.1941', '-0.3032', '-0.003986', '0.2966', '0.5557', '-0.1692', '-0.219', '1.091', '-0.3828', '0.1549', '-0.2483', '0.3784', '0.2445', '0.1284', '0.0883', '0.557', '-0.03485', '-0.2847', '1.021', '0.54', '-0.312', '-0.4482', '1.069', '-0.1677']",,,,,,,
mondo:0013267,distal 16p11.2 microdeletion syndrome,"['chromosome 16p11.2 deletion syndrome, 220kb', 'obesity, susceptibility to', 'distal monosomy 16p11.2', 'distal del(16)(p11.2)', 'chromosome 16p11.2 deletion syndrome, type 220kb', 'body mass index QTL16', 'chromosome 16p11.2 deletion syndrome, 220-KB', 'distal 16p11.2 microdeletion syndrome', 'body Mass index quantitative trait locus 16']",0060398,613444,261222,C4518824,,,,,,,,
mondo:0013268,frontonasal dysplasia with alopecia and genital anomaly,"['craniofrontonasal dysplasia with alopecia and hypogonadism', 'FND2', 'ALX4-related FNDAG', 'frontonasal dysplasia 2', 'frontonasal dysplasia type 2', 'frontonasal dysplasia with alopecia and genital abnomality']",0081046,613451,228390,C3150703,"['-0.416', '0.1443', '0.2372', '-0.521', '0.5293', '-0.404', '-0.5527', '0.8643', '-0.322', '-0.136', '-0.2559', '-0.3567', '0.611', '-0.3293', '0.03195', '0.03198', '0.4238', '0.292', '-0.4995', '-0.8784', '-0.342', '0.0761', '0.51', '-0.3877', '0.739', '0.02914', '-0.1348', '-0.152', '0.6846', '-0.4036', '0.2915', '-0.1708', '-0.05896', '-0.0866', '0.2056', '-0.6157', '-0.1962', '-0.6753', '-0.01689', '-0.517', '-0.11884', '-0.0916', '-0.03748', '-0.4402', '-0.0674', '-0.3826', '-0.11816', '-0.0675', '-0.517', '-0.88', '-0.08356', '-0.5347', '-0.0738', '0.5796', '-0.526', '-0.4607', '0.287', '0.00909', '0.01698', '0.3115', '0.201', '-0.11237', '0.01545', '0.5435', '0.02744', '0.2439', '0.03754', '0.2961', '-0.1702', '0.03317', '-0.267', '0.3462', '0.3787', '-0.0997', '0.011795', '0.7046', '0.1747', '-0.1311', '0.218', '0.03067', '0.2131', '0.4333', '0.3042', '0.5713', '0.1626', '0.219', '-0.005573', '0.4463', '0.02197', '0.334', '-0.41', '0.5933', '0.4868', '-0.0653', '1.488', '0.3325', '0.07056', '-0.7583', '0.4238', '-0.02698']",,,,,,,
mondo:0013269,autosomal recessive nonsyndromic hearing loss 91,"['autosomal recessive deafness 91', 'autosomal recessive nonsyndromic deafness caused by mutation in SERPINB6', 'autosomal recessive nonsyndromic deafness 91', 'autosomal recessive nonsyndromic deafness type 91', 'deafness, autosomal recessive 91', 'SERPINB6 autosomal recessive nonsyndromic deafness', 'DFNB91', 'deafness, autosomal recessive type 91']",0110536,613453,,C3150704,,,,,,,,
mondo:0013270,"Rett syndrome, congenital variant","['Rett syndrome, congenital variant']",,613454,,C3150705,,C176903,,,,,,
mondo:0013271,frontonasal dysplasia - severe microphthalmia - severe facial clefting syndrome,"['FND3', 'ALX1-related frontonasal dysplasia', 'frontonasal dysplasia type 3', 'frontonasal dysplasia 3']",0081047,613456,306542,C3150706,"['-0.2316', '0.2642', '0.3713', '-0.3486', '0.2141', '-0.1545', '0.08185', '0.3586', '-0.3691', '-0.1906', '-0.06152', '-0.0902', '0.1293', '-0.2018', '-0.3079', '0.1663', '0.35', '-0.1564', '-0.24', '-0.469', '-0.129', '0.0747', '0.373', '-0.1404', '0.11743', '0.0958', '-0.2186', '-0.02289', '0.6113', '-0.3188', '0.2247', '0.005127', '0.2944', '0.287', '0.2235', '-0.2097', '0.07', '-0.1156', '-0.175', '-0.6816', '0.1382', '-0.006878', '-0.05966', '-0.3428', '-0.1749', '-0.2683', '-0.000587', '0.4023', '-0.0699', '-0.05457', '-0.2595', '-0.1793', '-0.106', '0.1414', '-0.4255', '-0.2751', '-0.00796', '-0.303', '-0.228', '0.0881', '0.2003', '0.2046', '-0.3833', '0.1487', '-0.003412', '-0.12134', '0.2952', '0.1126', '-0.2263', '0.3635', '-0.4392', '0.2566', '0.2751', '-0.0917', '-0.2357', '-0.006973', '0.2491', '-0.3044', '-0.313', '-0.0794', '0.1307', '0.0446', '-0.0932', '0.5874', '-0.0948', '-0.05652', '-0.2468', '0.4731', '0.1471', '0.02856', '-0.0514', '0.4153', '0.3865', '0.26', '0.7114', '-0.3147', '0.4106', '-0.5664', '0.2273', '0.3396']",,,,,,,
mondo:0013272,chromosome 14q11-q22 deletion syndrome,"['monosomy 14q11.2', 'chromosome 14q11-q22 deletion syndrome, isolated cases', '14q11.2 microdeletion syndrome', 'Del(14)(q11.2)', 'chromosome 14q11-q22 deletion syndrome']",0060392,613457,261120,C4304999,,,,,,,,
mondo:0013273,chromosome 16p13.3 duplication syndrome,"['16p13.3 microduplication syndrome', 'distal trisomy 16p', '16p13.3 duplication', 'chromosome 16p13.3 duplication syndrome, isolated cases', 'interstitial 16p13.3 duplication', 'dup(16)(p13.3)', 'distal duplication 16p', 'chromosome 16p13.3 duplication syndrome', 'chromosome 16p13.3 duplication', 'telomeric duplication 16p', 'trisomy 16pter']",0060431,613458,96078,C4518796,,,,,,,,
mondo:0013274,retinitis pigmentosa 51,"['TTC8 retinitis pigmentosa', 'retinitis pigmentosa 51', 'retinitis pigmentosa type 51', 'retinitis pigmentosa caused by mutation in TTC8', 'RP51']",0110398,613464,,C3150715,,,,,,H35.5,,
mondo:0013275,hemolytic anemia due to glucophosphate isomerase deficiency,"['hemolytic anemia, nonspherocytic, due to glucose phosphate isomerase deficiency', 'glucosephosphate isomerase deficiency']",,613470,712,CN072763,"['-0.4187', '0.365', '-0.2786', '0.1664', '0.4136', '0.01455', '-0.1124', '0.57', '-0.0988', '-0.5796', '0.5063', '-0.1165', '0.3591', '0.1187', '-1.14', '0.0175', '-0.6675', '0.1072', '-0.525', '-0.4912', '-0.1375', '-0.4265', '0.1714', '-0.3223', '0.4468', '-0.4973', '-0.1577', '-0.3306', '0.6245', '0.0555', '0.0323', '0.05472', '0.643', '0.4333', '0.4917', '-0.2793', '-0.5635', '-0.581', '0.4758', '-0.1539', '-0.806', '0.275', '-0.00973', '-0.5303', '-0.694', '-0.7036', '0.1519', '0.1543', '0.3088', '-0.3801', '0.4128', '0.428', '0.7173', '-0.2423', '0.5386', '-0.4993', '0.0801', '0.2448', '-0.9155', '-0.09607', '-0.001759', '0.05045', '-0.0638', '-0.2151', '0.01007', '0.2834', '0.189', '0.669', '-0.5547', '0.903', '0.809', '-0.2573', '-0.557', '-0.6655', '0.3662', '1.221', '0.4014', '0.185', '0.1035', '0.1658', '0.08026', '-0.03668', '0.0324', '0.03763', '0.5215', '-0.3955', '-0.829', '0.3103', '0.6953', '-0.3467', '0.691', '0.3313', '-0.2041', '-0.009186', '0.481', '1.123', '0.304', '0.1416', '0.4343', '-0.5737']",,,,,,,
mondo:0013276,Reynolds syndrome,"['primary biliary cirrhosis, Scleroderma, Raynaud disease, and telangiectasia', 'Reynolds syndrome', 'primary biliary cirrhosis and systemic scleroderma']",,613471,779,C0748397,"['-0.04138', '0.04858', '0.03108', '-0.01933', '0.01778', '-0.0817', '-0.01752', '0.0671', '-0.0662', '-0.03732', '-0.004963', '0.001096', '0.003227', '0.007744', '-0.009254', '-0.04202', '-0.00408', '-0.01459', '-0.01244', '-0.09973', '0.015305', '-0.03918', '0.04144', '-0.03687', '0.03287', '-0.002794', '-0.03452', '-0.03177', '0.0366', '-0.04388', '0.039', '-0.0027', '0.07434', '0.04858', '0.02905', '-0.0229', '-0.01093', '-0.02928', '-0.008995', '-0.0845', '0.02875', '-0.0666', '0.02977', '-0.04953', '0.001224', '-0.06396', '-0.0424', '0.053', '0.02103', '0.01027', '-0.00599', '0.001283', '0.001516', '-7.18e-05', '-0.0356', '-0.02528', '0.04648', '-0.02951', '-0.0776', '0.02003', '0.04236', '0.02924', '-0.00427', '0.01773', '0.005768', '0.007133', '0.05627', '0.0338', '-0.0564', '0.07227', '-0.07886', '0.006443', '0.00888', '-0.04346', '0.02156', '0.01432', '-0.0213', '0.003462', '-0.05353', '-0.0463', '0.0399', '0.0085', '-0.03143', '0.05505', '-0.014656', '-0.02226', '0.01526', '0.0667', '0.06232', '0.01836', '0.0405', '0.05157', '0.02632', '0.02238', '0.1364', '0.01881', '0.067', '-0.1054', '-0.004967', '0.01341']",,,,,,,
mondo:0013277,"developmental and epileptic encephalopathy, 5","['SPTAN1 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, type 5', 'early infantile epileptic encephalopathy caused by mutation in SPTAN1', 'EIEE5', 'developmental and epileptic encephalopathy 5', 'DEE5', 'epileptic encephalopathy, early infantile, 5']",0080438,613477,,C3150731,,,,,,,,
mondo:0013278,lymphatic malformation 3,"['LMPH1C', 'lymphedema, hereditary, type 1C', 'hereditary lymphedema caused by mutation in GJC2', 'lymphedema, hereditary, IC', 'GJC2 hereditary lymphedema', 'lymphedema, hereditary, 1C']",0070208,613480,,C3150732,,,,,,,,
mondo:0013279,long QT syndrome 13,"['LQT13', 'long QT syndrome 13', 'long QT syndrome type 13', 'long QT syndrome caused by mutation in KCNJ5', 'KCNJ5 long QT syndrome']",0110654,613485,101016,C3150733,"['-0.0118', '0.05048', '0.01287', '-0.01395', '0.003933', '-0.0703', '0.03375', '0.08545', '-0.0559', '-0.04224', '-0.01053', '0.00785', '0.03342', '0.017', '-0.0503', '-0.03818', '0.009315', '-0.03842', '-0.00999', '-0.10016', '0.011604', '-0.0066', '0.044', '-0.0326', '0.03867', '-0.0443', '-0.006542', '-0.01062', '0.01279', '-0.048', '0.0705', '-0.01791', '0.06354', '0.02692', '0.02016', '-0.05545', '0.0004368', '-0.04535', '-0.02513', '-0.0755', '0.0368', '-0.0867', '0.0335', '-0.03735', '0.0001161', '-0.04288', '-0.04434', '0.08777', '0.00738', '0.01417', '-0.0289', '-0.01233', '-0.012794', '0.0171', '-0.03035', '-0.0328', '0.05875', '-0.002089', '-0.0472', '0.01833', '0.04376', '0.01862', '-0.002419', '0.011734', '-0.01263', '-0.003515', '0.04977', '0.052', '-0.06213', '0.06775', '-0.05432', '0.01755', '0.03014', '-0.05246', '0.00749', '0.05017', '0.01356', '-0.02386', '-0.03665', '-0.02791', '0.00966', '0.004513', '0.001809', '0.0559', '-0.013306', '0.02574', '0.005432', '0.07214', '0.0691', '0.02351', '0.004204', '0.04135', '0.00436', '0.0332', '0.1268', '0.02513', '0.07916', '-0.104', '-0.02048', '0.02586']",,,,,,,
mondo:0013280,myxoid liposarcoma,"['myxoid liposarcoma (morphologic abnormality)', 'myxoid/round cell liposarcoma', 'myxoid liposarcoma', 'Myxoliposarcoma', 'mixed-type liposarcoma']",5709,613488,,,"['-0.587', '0.2109', '0.1252', '0.5605', '-0.010086', '-0.364', '0.1141', '0.319', '-0.272', '-0.001329', '0.5244', '0.2292', '-0.171', '0.2144', '-0.2593', '0.1952', '-0.3567', '-0.1099', '-0.1559', '-0.3525', '-0.00772', '0.01342', '0.1959', '0.2717', '0.49', '0.04736', '0.146', '0.1815', '-0.1774', '0.2622', '0.1793', '-0.3792', '0.2708', '-0.4333', '0.63', '0.1274', '-1.281', '0.6157', '0.1616', '-0.543', '-0.0874', '-0.7534', '-0.05783', '-0.412', '0.321', '-0.03207', '-0.2644', '0.1543', '0.595', '-0.578', '0.1752', '-0.1279', '0.328', '-0.0231', '-0.2081', '-0.3948', '-0.3848', '0.2185', '-0.668', '-0.308', '0.1727', '-0.3752', '-0.2854', '-0.3408', '-0.2725', '0.6836', '0.1348', '-0.1599', '0.3948', '0.5664', '-0.1897', '0.4717', '-0.004436', '-0.3306', '0.1556', '0.2186', '-0.0682', '0.4954', '-0.2365', '-0.4617', '-0.3647', '0.086', '-0.3757', '-0.4194', '-0.0763', '-0.4119', '0.282', '-0.01353', '0.6943', '-0.1278', '0.06836', '0.0703', '-0.0911', '0.3215', '0.526', '0.7295', '-0.2534', '-0.5024', '-0.04102', '0.4526']",C27781,0000613,D018208,171.9,,,
mondo:0013281,COG4-congenital disorder of glycosylation,"['congenital disorder of glycosylation type IIj', 'congenital disorder of glycosylation, type IIj', 'congenital disorder of glycosylation type 2j', 'CDG syndrome type IIj', 'CDG-IIj', 'carbohydrate deficient glycoprotein syndrome type IIj', 'CDG2J', 'COG4-CDG (CDG-IIj)', 'CDG IIj', 'COG4-CDG']",0070262,613489,263501,C3150736,"['-0.516', '0.3748', '0.1425', '-0.3948', '-0.08954', '-0.4204', '-0.03436', '0.395', '-0.077', '-0.4524', '-0.1388', '-0.02455', '0.05405', '-0.1821', '0.02812', '0.1013', '0.04025', '-0.2487', '0.1633', '-0.4758', '0.0335', '-0.02454', '0.1053', '-0.4143', '-0.1375', '0.324', '-0.1986', '-0.1978', '0.2915', '-0.5073', '0.04227', '0.28', '0.3171', '0.0778', '-0.3247', '-0.05206', '-0.2129', '-0.3071', '-0.0906', '-0.3533', '0.2556', '-0.6157', '-0.11237', '-0.3232', '0.2053', '0.1637', '-0.03207', '0.1002', '-0.1453', '0.2443', '-0.17', '0.2086', '-0.346', '0.4844', '-0.1586', '-0.4119', '0.362', '-0.1892', '-0.4927', '0.2747', '0.0944', '-0.3303', '0.3652', '0.02818', '-0.5977', '-0.3489', '0.4324', '0.463', '-0.5146', '0.2191', '-0.2515', '0.436', '-0.04407', '0.2396', '0.072', '0.559', '0.1954', '-0.1658', '-0.1993', '0.1241', '0.387', '0.04572', '0.05148', '0.791', '0.5186', '0.10406', '0.03314', '0.0786', '0.579', '-0.1292', '0.554', '0.4885', '0.0719', '0.5137', '0.667', '0.5063', '0.462', '-0.123', '0.4841', '-0.1115']",,,,,,,
mondo:0013282,alpha 1-antitrypsin deficiency,"['alpha-1-antitrypsin deficiency', 'AAT deficiency', 'A-1ATD', 'A1AT deficiency', 'A1ATD', 'hemorrhagic diathesis due to antithrombin pittsburgh', 'emphysema-cirrhosis, due to AAT deficiency', 'AATD', 'emphysema due to AAT deficiency', 'Alpha-1 antitrypsin deficiency', 'A1AD', 'deficiency in Alpa-1-proteinase inhibitor', 'ALPHA-1-antitrypsin deficiency', 'Alpha 1 antitrypsin deficiency']",13372,613490,60,C0221757,"['0.5713', '0.2206', '-0.847', '-0.2805', '0.04166', '-0.3633', '0.651', '0.5273', '-0.1687', '-0.1256', '0.05142', '0.1315', '-0.0793', '0.2644', '0.04413', '-0.1853', '-0.07904', '0.327', '0.1385', '-0.659', '-0.3562', '-0.7827', '1.071', '-0.6235', '-0.06604', '-0.03387', '0.519', '0.2834', '-0.3284', '-0.2876', '0.4924', '-0.033', '0.2445', '0.5747', '-0.0636', '-0.8164', '-0.8325', '-0.3435', '-0.0729', '0.3254', '-0.3555', '0.0274', '0.642', '-0.01869', '0.0604', '0.03406', '-0.4302', '-0.454', '0.134', '0.6924', '0.2245', '0.1512', '0.0795', '0.04156', '0.1094', '-0.11804', '-0.2803', '-0.0911', '-0.78', '-0.02443', '0.568', '0.421', '0.3948', '0.01526', '-0.05264', '-0.4563', '0.591', '0.1958', '-0.2379', '0.3325', '-0.339', '-0.2627', '0.295', '0.1638', '1.141', '0.2327', '0.081', '0.1844', '-0.1864', '-0.0956', '-0.635', '-0.1791', '-0.65', '0.02663', '-0.2651', '0.3176', '0.3313', '-0.1532', '0.25', '-0.1334', '0.39', '-0.365', '-0.758', '0.02493', '0.6133', '0.3328', '0.321', '-0.3418', '-0.378', '-0.539']",C84397,,D019896,273.4,E88.01,10001806,
mondo:0013283,"immunodeficiency, common variable, 3","['antibody deficiency due to CD19 defect', 'immunodeficiency, common variable, type 3', 'immunodeficiency, common variable, 3', 'CVID3']",0081146,613493,,C3150738,,,,,,,,
mondo:0013284,"immunodeficiency, common variable, 4","['antibody deficiency due to Baffr defect', 'immunodeficiency, common variable, 4', 'CVID4', 'immunodeficiency, common variable, type 4']",0081147,613494,,C3150739,,,,,,,,
mondo:0013285,"immunodeficiency, common variable, 5","['CVID5', 'MS4A1 common variable immunodeficiency', 'immunodeficiency, common variable, type 5', 'antibody deficiency due to CD20 defect', 'immunodeficiency, common variable, 5', 'common variable immunodeficiency caused by mutation in MS4A1']",0081148,613495,,C3150740,,,,,,,,
mondo:0013286,"immunodeficiency, common variable, 6","['immunodeficiency, common variable, type 6', 'immunodeficiency, common variable, 6', 'common variable immunodeficiency caused by mutation in CD81', 'antibody deficiency due to CD81 defect', 'CD81 common variable immunodeficiency', 'CVID6']",0081149,613496,,C3150741,,,,,,,,
mondo:0013287,"agammaglobulinemia 2, autosomal recessive","['agammaglobulinemia 2, autosomal recessive', 'lambda 5 deficiency', 'IGLL1 autosomal agammaglobulinemia', 'AGM2', 'agammaglobulinemia, autosomal recessive, due to IGLL1 defect', 'autosomal agammaglobulinemia caused by mutation in IGLL1']",0081135,613500,,C3150750,,,,,,,,
mondo:0013288,"agammaglobulinemia 3, autosomal recessive","['agammaglobulinemia 3, autosomal recessive', 'AGM3', 'agammaglobulinemia, autosomal recessive, due to Cd79A defect', 'CD79A autosomal agammaglobulinemia', 'autosomal agammaglobulinemia caused by mutation in CD79A']",0081137,613501,,C3150751,,,,,,,,
mondo:0013289,"agammaglobulinemia 4, autosomal recessive","['AGM4', 'autosomal agammaglobulinemia caused by mutation in BLNK', 'agammaglobulinemia 4, autosomal recessive', 'agammaglobulinemia 4', 'BLNK autosomal agammaglobulinemia', 'agammaglobulinemia, autosomal recessive, due to Blnk defect']",,613502,,C3150752,,,,,,,,
mondo:0013290,"agammaglobulinemia 5, autosomal dominant","['LRRC8A autosomal agammaglobulinemia', 'agammaglobulinemia 5', 'AGM5', 'agammaglobulinemia, autosomal dominant, due to Lrrc8A defect', 'autosomal agammaglobulinemia caused by mutation in LRRC8A', 'agammaglobulinemia 5, autosomal dominant']",0080588,613506,,C3150753,,,,,,,,
mondo:0013291,glycogen storage disease XV,"['glycogen storage disease XV', 'glycogenin deficiency', 'glycogen storage disease type XV', 'GSD type XV', 'GSD15', 'glycogenosis type 15', 'GSD 15', 'glycogen storage disease type 15', 'glycogenosis with severe cardiomyopathy due to glycogenin deficiency', 'Gyg1 deficiency', 'glycogen storage disease 15', 'glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency', 'glycogenosis type XV', 'GSD type 15', 'GSD with severe cardiomyopathy due to glycogenin deficiency']",0050579,613507,263297,C3150754,"['-0.4949', '0.1929', '0.003836', '0.1831', '0.4817', '-0.6494', '-0.2357', '0.6006', '-0.2322', '-0.01539', '-0.2137', '-0.233', '0.1387', '-0.0776', '0.1622', '-0.04614', '-0.492', '-0.1166', '-0.883', '-0.6445', '0.346', '-0.1705', '0.3225', '-0.0478', '-0.2054', '-0.1031', '0.118', '0.1415', '-0.2252', '-0.01175', '0.638', '0.3918', '0.6426', '-0.1345', '-0.1768', '-0.6797', '-0.2228', '-0.0729', '0.04218', '-0.2954', '-0.02817', '-0.1245', '0.1444', '0.08966', '-0.3032', '0.006195', '0.0742', '0.0191', '-0.2976', '0.1508', '-0.11273', '0.2024', '0.08356', '0.1252', '-0.2025', '-1.126', '0.4368', '0.1499', '-0.04846', '0.05426', '0.3613', '0.1259', '0.2463', '-0.2566', '-0.559', '0.0723', '0.10455', '0.36', '-0.87', '-0.1182', '-0.3958', '-0.1836', '-0.0157', '0.223', '0.2754', '0.372', '0.07043', '0.4148', '-0.4468', '0.0005155', '0.1487', '-0.02373', '0.1451', '-0.1638', '0.04843', '-0.1235', '0.5596', '0.564', '0.2025', '0.233', '0.1139', '-0.03925', '-0.08344', '-0.2512', '0.82', '0.4858', '0.4004', '-0.1803', '-0.05374', '-0.03754']",,,,,,,
mondo:0013292,chromosome 4q21 deletion syndrome,"['4q21 microdeletion syndrome', 'chromosome 4q21 deletion syndrome, isolated cases', 'Del(4)(q21)', 'chromosome 4q21 deletion syndrome', 'monosomy 4q21']",0060420,613509,238750,C4304530,,,,,,,,
mondo:0013293,isolated microphthalmia 6,"['MCOP6', 'microphthalmia, posterior nonsyndromic', 'PRSS56 isolated microphthalmia', 'microphthalmia, isolated 6', 'isolated microphthalmia type 6', 'microphthalmia, isolated type 6', 'isolated microphthalmia caused by mutation in PRSS56', 'posterior nonsyndromic microphthalmia']",0060835,613517,,C3150757,,,,,,,,
mondo:0013294,"dermatitis, atopic, 8","['ATOD8', 'dermatitis, atopic, 8', 'dermatitis, atopic, severity of', 'dermatitis, atopic, susceptibility to, 8', 'atopic dermatitis type 8']",0110104,613518,,C3150763,,,,,,,,
mondo:0013295,"dermatitis, atopic, 9","['dermatitis, ATOPIC, 9', 'ATOD9', 'dermatitis, atopic, susceptibility to, 9', 'atopic dermatitis type 9']",0110105,613519,,C3150764,,,,,,,,
mondo:0013296,myeloid neoplasm associated with FGFR1 rearrangement,"['8p11 stem cell leukemia/lymphoma syndrome', 'myeloid/lymphoid neoplasm associated with FGFR1 rearrangement', 'myeloid/lymphoid neoplasms with FGFR1 rearrangement', '8p11 myeloproliferative syndrome', 'stem cell leukemia/lymphoma', 'myeloid and lymphoid neoplasms with FGFR1 rearrangement', 'chromosome 8p11 myeloproliferative syndrome', '8p11 stem cell syndrome', '8p11 stem cell lymphoma/leukemia syndrome']",,613523,168953,C3150773,,C84277,,,,,,
mondo:0013297,autosomal dominant limb-girdle muscular dystrophy type 1H,"['LGMD1H', 'muscular dystrophy limb-girdle type 1H', 'muscular dystrophy, limb-girdle, type 1H', 'limb-girdle muscular dystrophy type 1H']",0110303,613530,238755,C3150786,,,,,,,,
mondo:0013298,chromosome 17q21.31 duplication syndrome,"['17q21.31 microduplication syndrome', 'trisomy 17q21.31', 'chromosome 17q21.31 duplication syndrome', 'dup(17)(q21.31)']",0060434,613533,217340,C4274345,,,,,,,,
mondo:0013299,chromosome 6q11-q14 deletion syndrome,"['chromosome 6Q13-q14 deletion syndrome', 'chromosome 6q11-q14 deletion syndrome', 'chromosome 6q11-q14 deletion syndrome, isolated cases']",0060423,613544,,C3150790,,,,,,,,
mondo:0013300,commissural facial cleft,"['lateral cleft, isolated', 'commissural cleft, isolated', 'transverse cleft, isolated', 'macrostomia', 'macrostomia, isolated']",,613545,141276,,,,,D008265,744.83,,,
mondo:0013301,aromatase deficiency,"['aromatase deficiency', 'congenital estrogen deficiency', 'pseudohermaphroditism, female, due to placental aromatase deficiency', 'congenital oestrogen deficiency']",,613546,91,C1960539,"['-0.354', '0.3186', '-0.0686', '-0.12006', '0.4912', '-0.2593', '-0.299', '0.533', '-0.4075', '-0.4287', '-0.0639', '0.05685', '0.3398', '0.5645', '-0.01393', '0.11786', '0.5225', '0.19', '-0.9478', '-0.2239', '-0.029', '-0.3372', '0.3223', '-0.59', '0.162', '0.07983', '0.0546', '-0.1697', '-0.234', '-0.4478', '0.696', '-0.0434', '0.7812', '0.2727', '-0.2472', '-0.03595', '0.7437', '-0.4478', '0.03143', '0.2377', '0.721', '0.664', '0.02943', '0.2493', '-0.3235', '-0.4292', '-0.00877', '0.3972', '-0.486', '0.3372', '0.03082', '-0.4907', '0.07227', '0.3867', '-0.6616', '-0.01239', '0.624', '-0.4438', '-0.0779', '0.3564', '0.3735', '0.5063', '0.1483', '0.11414', '-0.3389', '-0.02977', '0.6006', '0.4714', '-0.1125', '-0.0612', '0.7383', '-0.1531', '0.316', '-0.2527', '0.389', '-0.2399', '-0.2223', '0.1722', '-0.1456', '-0.535', '-0.10767', '0.1768', '-0.11456', '-0.718', '-0.0821', '0.5557', '0.05344', '-0.3506', '0.749', '0.1104', '0.4272', '0.4966', '-0.4612', '0.11053', '0.818', '-0.5386', '0.1471', '0.3313', '0.0597', '0.397']",C120144,,C537436,,,,
mondo:0013302,nephronophthisis 11,"['NPHP11', 'nephronophthisis 11', 'nephronophthisis type 11']",0111118,613550,,C3150796,,,,,,,,
mondo:0013303,"autoimmune disease, susceptibility to, 6","['AIS6', 'SIAE autoimmune disease', 'autoimmune disease, susceptibility to, type 6', 'susceptibility to autoimmune disease 6', 'autoimmune disease, susceptibility to, 6', 'autoimmune disease caused by mutation in SIAE']",,613551,,,,,,,,,,
mondo:0013304,von Willebrand disease 2,"['Von Willebrand disease, type 2', 'von willebrand^s disease 2', 'VWD2', 'von Willebrand^s disease type 2', 'von Willebrand disease type II', 'Von Willebrand disease, type 2N', 'Von Willebrand disease, type 2A', 'VWD, type 2', 'VWD type 2', 'Von Willebrand disease, type 2B', 'Von Willebrand disease, type 2M', 'VON WILLEBRAND disease, type 2', 'von Willebrand disease type 2', 'von Willebrand disease, types 2A, 2B, 2M, and 2N']",0060574,613554,166081,C1264040,"['-0.2261', '0.4026', '-0.384', '0.332', '-0.1482', '0.03287', '2.337e-05', '0.2524', '-0.2903', '-0.627', '0.2637', '0.5684', '0.637', '0.819', '-0.031', '-0.688', '0.2213', '0.0764', '-0.1089', '-0.6655', '-0.2527', '-0.8276', '1.222', '0.012146', '0.0451', '-0.1167', '-0.3972', '-0.1213', '0.8447', '0.115', '0.702', '0.0622', '0.256', '0.10736', '0.2817', '-0.6045', '-0.4133', '-0.1646', '0.1456', '-0.2827', '0.822', '-0.2223', '0.4392', '-0.5835', '0.6895', '-0.51', '-0.7295', '0.1055', '0.0106', '-0.3396', '0.643', '-0.0707', '0.2334', '-0.007576', '-0.178', '-0.2988', '-1.049', '0.9814', '-0.8086', '-0.3962', '-0.5957', '0.1862', '0.62', '-0.584', '0.2732', '-0.06247', '-0.10284', '-0.807', '-1.079', '0.338', '-0.1733', '0.01017', '-0.3215', '-0.8574', '0.8296', '0.5854', '1.028', '0.4111', '0.3872', '-0.397', '-0.6333', '-0.2778', '0.6255', '-0.5693', '-0.2935', '0.3955', '-0.01778', '0.3582', '-0.01834', '0.11786', '-0.4849', '0.5835', '0.2065', '-0.12335', '0.9863', '0.603', '0.03885', '-0.786', '-0.588', '0.2917']",,,D056728,,,,
mondo:0013305,autosomal dominant nonsyndromic hearing loss 51,"['chromosome 9Q21.11 Duplication syndrome', 'autosomal dominant nonsyndromic deafness type 51', 'deafness, autosomal dominant type 51', 'autosomal dominant deafness 51', 'autosomal dominant nonsyndromic deafness 51', 'deafness, autosomal dominant 51', 'DFNA51', 'chromosome 9q21.11 duplication syndrome']",0110577,613558,,C3160736,,,,,,,,
mondo:0013306,combined oxidative phosphorylation defect type 7,"['COXPD7', 'combined oxidative phosphorylation deficiency 7', 'severe C12ORF65-related combined oxidative phosphorylation defect', 'combined oxidative phosphorylation deficiency caused by mutation in C12ORF65', 'C12ORF65 combined oxidative phosphorylation deficiency', 'severe C12ORF65-related COXPD', 'combined oxidative phosphorylation deficiency type 7', 'C12orf65 combined oxidative phosphorylation deficiency']",0111487,613559,254930,C3150801,"['-0.5625', '0.04364', '-0.010124', '-0.0204', '-0.4543', '-1.152', '0.1162', '0.7', '-0.7725', '0.05618', '-0.1412', '-0.0957', '-0.06207', '0.2053', '-0.1638', '-0.3647', '-0.11914', '-0.6445', '0.02394', '-0.5415', '0.04303', '-0.522', '0.1666', '0.1549', '0.1487', '-0.04132', '-0.2284', '0.4727', '-0.4866', '0.2164', '0.2734', '0.6885', '0.4207', '0.0793', '-0.1586', '-0.545', '0.0467', '0.1403', '-0.3643', '-0.08594', '-0.114', '-0.253', '-0.3254', '0.4985', '-0.2302', '-0.337', '-0.0875', '0.087', '-0.2888', '-0.4346', '-0.3613', '0.527', '-0.2086', '-0.239', '0.238', '-0.552', '0.1571', '-0.0936', '0.2227', '0.1506', '0.152', '0.3335', '0.2595', '0.2668', '-0.2866', '0.1736', '0.5474', '0.2634', '-0.07227', '0.5635', '-0.1963', '0.3005', '-0.01026', '0.0683', '0.4614', '0.006256', '0.0775', '-0.2341', '0.2856', '0.572', '0.2217', '0.042', '0.2903', '0.551', '-0.01002', '-0.1993', '0.2067', '0.1342', '0.9697', '-0.2235', '0.541', '0.5337', '0.05402', '0.143', '0.4373', '0.2109', '-0.04816', '-0.0643', '0.28', '0.4285']",,,,,,,
mondo:0013307,"myopathy, lactic acidosis, and sideroblastic anemia 2","['myopathy, lactic acidosis, and sideroblastic anemia 2', 'mitochondrial myopathy and sideroblastic anaemia caused by mutation in YARS2', 'myopathy, lactic acidosis, and sideroblastic Anemia type 2', 'myopathy, lactic acidosis, and sideroblastic Anaemia type 2', 'MLASA2', 'YARS2 mitochondrial myopathy and sideroblastic anemia', 'YARS2 mitochondrial myopathy and sideroblastic anaemia', 'mitochondrial myopathy and sideroblastic anemia caused by mutation in YARS2']",0111186,613561,,C3150802,,,,,,,,
mondo:0013308,CBL-related disorder,"['Cbl mutation-associated syndrome', 'Noonan syndrome-like disorder with juvenile myelomonocytic leukaemia', 'Noonan syndrome-like disorder with or without juvenile myelomonocytic leukaemia', 'NSLL', 'Noonan syndrome-like disorder with JMML', 'Noonan syndrome-like disorder with or without juvenile myelomonocytic leukemia', 'Cbl syndrome']",,613563,363972,C4016301,"['0.02173', '0.05353', '0.0864', '-0.2278', '0.1702', '-0.236', '0.6294', '0.4712', '-0.289', '-0.5146', '0.4417', '0.1519', '0.1582', '-0.3567', '-0.0839', '0.1807', '-0.1633', '-0.615', '-0.4575', '-0.3232', '0.2306', '-0.09106', '0.727', '-0.3062', '0.413', '0.0623', '0.0828', '0.1554', '0.4456', '-0.356', '0.6143', '-0.2063', '0.6836', '0.561', '0.4807', '-0.0827', '-0.2292', '0.3472', '-0.1694', '-0.668', '-0.01164', '-0.191', '0.1654', '-0.4658', '0.0849', '-0.02168', '0.1462', '0.57', '-0.1511', '0.0007305', '-0.554', '0.2954', '-0.597', '0.2847', '0.1869', '-0.4622', '-0.299', '-0.04984', '-0.13', '0.499', '0.204', '-0.1973', '0.2393', '0.0699', '0.2842', '0.2379', '-0.12274', '0.3013', '0.11835', '0.8013', '-0.1066', '0.05334', '0.1908', '0.574', '-0.1642', '-0.1741', '0.1133', '-0.208', '-0.0774', '-0.2097', '0.1967', '0.1533', '-0.4844', '0.583', '-0.743', '-0.3096', '0.5986', '0.185', '0.539', '0.5264', '0.0007706', '0.05264', '-0.2123', '-0.1321', '0.2426', '0.2834', '0.706', '0.06885', '-0.08374', '0.0721']",,,,,,,
mondo:0013309,chromosome 2p12-p11.2 deletion syndrome,['chromosome 2p12-p11.2 deletion syndrome'],0060414,613564,,C3150804,,,,,,,,
mondo:0013310,congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency,"['POR deficiency', 'disordered steroidogenesis due to cytochrome P450 oxidoreductase', 'PORD', 'disordered steroidogenesis due to cytochrome P450 oxidoreductase deficiency', 'congenital adrenal hyperplasia due to cytochrome POR deficiency', 'adrenal hyperplasia, congenital, due to cytochrome P450 oxidoreductase deficiency', 'disordered steroidogenesis due to POR deficiency']",0080925,613571,95699,,"['-0.7563', '0.555', '-0.735', '-0.4243', '0.4377', '-0.2625', '-0.9033', '1.505', '-0.6133', '-1.187', '0.522', '-0.2008', '-0.07794', '1.643', '-0.5913', '0.3835', '-0.0949', '0.1932', '-0.532', '-0.2573', '-0.08997', '-0.1718', '0.10767', '0.2302', '0.2463', '0.2854', '0.06964', '-0.0234', '1.558', '-0.6997', '0.2474', '-0.02654', '0.534', '-0.03854', '0.1439', '0.537', '-0.0408', '0.3445', '0.1782', '-0.769', '0.3218', '-0.10785', '-0.0908', '-0.5913', '0.1724', '-0.9937', '0.1434', '0.244', '0.4802', '0.764', '0.1545', '-0.4019', '0.1544', '-0.6997', '-0.1377', '-0.3428', '-0.0278', '-0.4773', '-0.0765', '0.4795', '-0.3188', '-0.03577', '0.7646', '-0.4934', '0.625', '1.135', '0.202', '0.3367', '-0.475', '0.5415', '-0.506', '0.772', '0.2778', '0.02193', '-0.1742', '-0.541', '-0.2434', '-0.3206', '-0.11536', '0.05063', '0.3557', '0.0718', '-0.0768', '-0.637', '0.5264', '0.249', '-0.05', '-0.5854', '0.4656', '0.2047', '0.2605', '0.2844', '-0.1405', '0.004498', '0.2925', '0.1328', '0.2499', '-0.541', '0.11926', '0.104']",C174439,,,,,,
mondo:0013311,ectodermal dysplasia-syndactyly syndrome,"['ectodermal dysplasia-syndactyly syndrome type 1', 'EDSS', 'EDSS1', 'ectodermal dysplasia-syndactyly syndrome 1']",,,247820,CN228599,"['-0.0743', '0.2603', '0.2632', '-0.2072', '0.3486', '-0.277', '-0.03595', '0.2494', '-0.0975', '-0.2489', '-0.2163', '-0.09503', '-0.2471', '-0.148', '-0.2146', '0.1746', '0.464', '-0.326', '-0.1239', '-0.536', '-0.386', '0.0297', '0.3782', '-0.1655', '0.1705', '0.1287', '-0.4631', '0.2983', '0.3074', '-0.295', '0.1625', '-0.1932', '-0.012695', '0.1793', '0.3882', '-0.2448', '0.04453', '-0.2136', '-0.1024', '-0.4497', '0.1525', '-0.1077', '-0.1549', '-0.361', '-0.0713', '-0.3032', '-0.11945', '0.4272', '0.1068', '-0.3464', '-0.2006', '-0.0512', '0.1349', '0.02553', '-0.4026', '-0.2517', '0.1617', '-0.336', '-0.271', '-0.2029', '0.2338', '0.3071', '-0.2174', '0.0642', '-0.05154', '0.1246', '0.2693', '0.3513', '-0.00726', '0.418', '-0.4329', '-0.02168', '0.2515', '-0.1064', '0.02368', '-0.3179', '0.15', '-0.2778', '-0.0564', '-0.2142', '0.0665', '0.0963', '0.0781', '0.1787', '-0.01955', '-0.06866', '-0.1908', '0.358', '0.318', '0.2339', '0.03214', '0.4084', '0.2316', '0.3123', '0.578', '-0.10077', '0.2427', '-0.5493', '0.2418', '0.458']",,,,,,,
mondo:0013312,retinitis pigmentosa 55,"['ARL6 retinitis pigmentosa', 'retinitis pigmentosa type 55', 'RP55', 'retinitis pigmentosa 55', 'retinitis pigmentosa caused by mutation in ARL6']",0110370,613575,,C3150808,,,,,,H35.5,,
mondo:0013313,ectodermal dysplasia-cutaneous syndactyly syndrome,"['ectodermal dysplasia-syndactyly syndrome 2', 'EDSS2', 'EDCS']",,613576,247827,C3150809,,,,,,,,
mondo:0013314,retinitis pigmentosa 56,"['retinitis pigmentosa 56', 'maculopathy, Impg2-related', 'retinitis pigmentosa caused by mutation in IMPG2', 'IMPG2 retinitis pigmentosa', 'retinitis pigmentosa type 56', 'RP56']",0110371,613581,,C3150819,,,,,,H35.5,,
mondo:0013315,retinitis pigmentosa 57,"['retinitis pigmentosa caused by mutation in PDE6G', 'retinitis pigmentosa type 57', 'RP57', 'PDE6G retinitis pigmentosa', 'retinitis pigmentosa 57']",0110407,613582,,C3150821,,,,,,H35.5,,
mondo:0013316,occult macular dystrophy,"['OCMD', 'OMD', 'occult macular dystrophy', 'Omd']",0050578,613587,247834,C3150833,"['-0.3845', '-0.02084', '0.0698', '-0.01509', '0.1613', '-0.4697', '-0.0925', '0.1927', '-0.508', '0.02513', '-0.1323', '-0.2595', '-0.385', '-0.3223', '0.314', '-0.2986', '0.3728', '-0.3513', '-0.0923', '-0.74', '-0.045', '0.03168', '0.15', '0.422', '0.0362', '-0.02824', '-0.1159', '-0.12', '-0.4639', '0.627', '0.35', '0.004215', '0.2087', '-0.138', '0.2288', '0.0341', '-0.12115', '-0.1257', '0.02498', '-0.3748', '0.3376', '-0.4678', '0.1219', '-0.05612', '-0.189', '0.02841', '-0.4756', '-0.267', '0.06146', '0.161', '0.3044', '0.3335', '0.10626', '0.05295', '0.05942', '-0.1582', '0.729', '-0.2703', '-0.539', '-0.02568', '0.1539', '0.03735', '0.4338', '0.02806', '0.001269', '0.2008', '0.548', '0.558', '-0.2512', '0.4514', '-0.303', '-0.4062', '0.2852', '0.2847', '0.4067', '-0.4377', '0.3074', '0.2083', '-0.2345', '-0.02196', '0.05722', '0.010605', '0.05563', '0.3948', '-0.1658', '-0.615', '0.11816', '0.3704', '0.2954', '0.3682', '0.1753', '0.322', '0.01359', '0.1234', '0.443', '0.005066', '0.26', '-0.3271', '-0.02179', '0.2974']",,,,,H35.5,,
mondo:0013317,torsade-de-pointes syndrome with short coupling interval,"['torsade DE pointes, short-coupled variant']",,613600,51084,C3150851,,,,,,,,
mondo:0013318,early repolarization associated with ventricular fibrillation,"['early repolarization associated with ventricular fibrillation', 'early repolarization syndrome']",,613601,,C3150852,,,,,,,,
mondo:0013319,chromosome 4Q32.1-q32.2 triplication syndrome,['chromosome 4Q32.1-q32.2 triplication syndrome'],,613603,,C3150857,,,,,,,,
mondo:0013320,chromosome 16p12.2-p11.2 deletion syndrome,"['monosomy 16p11.2-p12.2', '16p11.2-p12.2 microdeletion syndrome', 'chromosome 16p12.2-p11.2 deletion syndrome, isolated cases', 'monosomy 16p11.2p12.2', 'Del(16)(p11.2p12.2)', '16p11.2p12.2 microdeletion syndrome', 'chromosome 16p12.2-p11.2 deletion syndrome, 7.1- to 8.7-MB']",0060400,613604,261211,C4304597,,,,,,,,
mondo:0013321,forsythe-wakeling syndrome,"['FWS', 'microcephaly and Growth retardation with childhood-onset nephrotic syndrome and thrombocytopenia', 'FORSYTHE-WAKELING syndrome']",,613606,,C3150859,,,,,,,,
mondo:0013322,"epilepsy, familial adult myoclonic, 3","['FAME3', 'epilepsy, familial ADULT myoclonic, 3', 'cortical myoclonic tremor with epilepsy, familial, 3']",0111695,613608,,C3150860,,,,C567098,,,,
mondo:0013323,cranioectodermal dysplasia 2,"['WDR35 cranioectodermal dysplasia', 'cranioectodermal dysplasia 2', 'cranioectodermal dysplasia caused by mutation in WDR35', 'CRANIOECTODERMAL dysplasia 2', 'CED2', 'Cranioectodermal dysplasia type 2']",0080804,613610,,C3150874,,,,,,,,
mondo:0013324,lymphedema-posterior choanal atresia syndrome,"['CATLPH', 'choanal atresia and lymphedema']",,613611,99141,C3150875,,,,,,Q82.0,,
mondo:0013325,COG5-congenital disorder of glycosylation,"['CDG III', 'carbohydrate deficient glycoprotein syndrome type III', 'congenital disorder of glycosylation type III', 'CDG-III', 'COG5-CDG', 'COG5-CDG (CDG-III)', 'CDG syndrome type III', 'CDG syndrome type 3', 'congenital disorder of glycosylation type 2i', 'congenital disorder of glycosylation, type III', 'CDG2I']",0070261,613612,263487,C3150876,"['-0.5605', '0.1531', '0.014984', '-0.327', '-0.1487', '-0.601', '-0.1989', '0.376', '-0.432', '-0.4443', '-0.3896', '0.2551', '0.1317', '-0.1771', '0.4187', '-0.002432', '0.347', '-0.0918', '-0.1403', '-0.6714', '0.02916', '-0.1081', '-0.09644', '-0.6504', '0.0809', '0.1', '-0.02942', '-0.1886', '0.4443', '-0.4568', '-0.317', '0.3638', '0.3215', '0.01101', '-0.6064', '-0.4734', '-0.2876', '-0.1976', '-0.63', '-0.3806', '0.0012045', '-0.627', '-0.0904', '-0.2144', '0.302', '-0.01994', '-0.0915', '0.2632', '-0.0946', '-0.2651', '-0.2688', '0.3284', '-0.3052', '0.10895', '0.05658', '-0.6323', '0.1724', '-0.2512', '-0.5513', '0.1405', '0.2021', '-0.1672', '0.4124', '0.04416', '-0.1854', '-0.3164', '0.3044', '0.3374', '-0.547', '0.2249', '-0.2018', '0.07', '-0.15', '-0.1995', '0.12164', '0.3848', '0.149', '-0.03604', '-0.0419', '0.428', '0.1124', '-0.10187', '-0.1976', '0.5234', '0.1932', '0.1678', '-0.1523', '0.09796', '0.7207', '0.2734', '0.3013', '0.792', '-0.2983', '0.4138', '0.783', '0.3992', '-0.0824', '-0.1616', '0.637', '0.0636']",,,,,,,
mondo:0013326,Senior-Loken syndrome 7,"['SENIOR-Loken syndrome 7', 'Senior-Loken syndrome type 7', 'Senior-Loken syndrome caused by mutation in SDCCAG8', 'SDCCAG8 Senior-Loken syndrome', 'SLSN7', 'Senior-Loken syndrome 7']",,613615,,C3150877,,,,,,,,
mondo:0013327,primary hyperoxaluria type 3,"['PH III', 'primary hyperoxaluria type III', 'HOGA1 primary hyperoxaluria', 'HP3', 'hyperoxaluria, primary, type III', 'hyperoxaluria, primary, type 3', 'primary hyperoxaluria caused by mutation in HOGA1']",0111672,613616,93600,C3150878,"['-0.2401', '0.226', '-0.00683', '-0.00976', '0.2227', '-0.1477', '-0.1687', '-5.686e-05', '-0.253', '0.2065', '-0.02979', '0.0924', '-0.04346', '-0.11743', '-0.1141', '-0.11975', '0.07495', '0.03125', '-0.1212', '-0.4556', '-0.04752', '-0.2052', '0.4158', '-0.1312', '-0.005184', '0.1273', '-0.0577', '-0.2496', '-0.04797', '-0.1404', '0.1478', '0.2087', '0.2603', '0.1283', '-0.2998', '-0.538', '0.1565', '-0.1255', '-0.08875', '-0.2773', '0.02985', '-0.4604', '0.2688', '-0.0601', '-0.3958', '-0.264', '-0.02945', '0.0775', '0.2869', '0.2727', '0.1169', '-0.1237', '0.2305', '-0.2004', '-0.2496', '-0.251', '0.4365', '-0.1309', '-0.3918', '0.1693', '0.401', '0.1312', '0.3926', '-0.339', '0.132', '0.009926', '0.2693', '0.1791', '-0.327', '-0.1509', '-0.2656', '-0.1638', '0.1069', '-0.07275', '0.2695', '0.07654', '-0.01788', '0.2015', '-0.2325', '0.04858', '-0.04016', '0.1974', '-0.0558', '0.1018', '0.04495', '0.0322', '0.2595', '0.1693', '0.3572', '0.078', '0.1368', '0.2157', '-0.1456', '-0.2411', '0.527', '0.3364', '0.544', '-0.4045', '-0.07684', '0.1511']",C123214,,,,,,
mondo:0013328,retinitis pigmentosa 58,"['RP58', 'ZNF513 retinitis pigmentosa', 'retinitis pigmentosa type 58', 'retinitis pigmentosa 58', 'retinitis pigmentosa caused by mutation in ZNF513']",0110362,613617,,C3150879,,,,,,H35.5,,
mondo:0013329,familial clubfoot due to 17q23.1q23.2 microduplication,"['hereditary clubfoot due to 17q23.1-q23.2 microduplication', 'chromosome 17q23.1-q23.2 DUPLICATION syndrome']",,613618,238578,C3150880,,,,,,,,
mondo:0013330,agenesis of the corpus callosum and congenital lymphedema,['agenesis of the corpus callosum and congenital lymphedema'],,613623,,C3150887,,,,,,,,
mondo:0013331,"factor 5 and Factor VIII, combined deficiency of, 2","['factor V and factor VIII, combined deficiency of', 'combined deficiency of factor V and factor VIII caused by mutation in MCFD2', 'factor V and factor VIII, combined deficiency of, 2', 'MCFD2 combined deficiency of factor V and factor VIII', 'factor 5 and Factor VIII, combined deficiency of, type 2', 'F5F8D2']",,613625,,C3150889,,,,,,,,
mondo:0013332,"brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability","['Tsukahara syndrome', 'brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and intellectual disability', 'brachydactyly, type A1, with short stature, scoliosis, microcephaly, ptosis, hearing loss, and mental retardation']",,613627,,C3150890,,,,,,,,
mondo:0013333,odontoid hypoplasia,['odontoid hypoplasia'],,613628,,,,C86969,,,,,,
mondo:0013334,cocoon syndrome,"['fetal encasement syndrome', 'foetal encasement syndrome', 'cocoon syndrome']",0060647,613630,465824,C3150891,"['-0.0351', '0.0626', '0.02724', '-0.000635', '0.02234', '-0.06683', '-0.00268', '0.0468', '-0.03075', '-0.02722', '-0.0202', '-0.003687', '0.00274', '0.01787', '-0.0345', '-0.04153', '-0.02869', '0.003944', '-0.01498', '-0.07623', '-0.01135', '-0.03226', '0.03616', '-0.02531', '0.02768', '-0.004715', '-0.02524', '-0.01559', '0.01915', '-0.0406', '0.03793', '0.0004344', '0.0686', '0.01608', '0.03473', '-0.04144', '-0.00614', '-0.02913', '-0.01344', '-0.07654', '0.02754', '-0.0702', '0.01498', '-0.03403', '0.01753', '-0.0682', '-0.03452', '0.05344', '0.01822', '0.007427', '-0.02422', '-0.01839', '0.01596', '0.024', '-0.04343', '-0.00899', '0.05145', '-0.01843', '-0.07227', '0.003805', '0.03384', '0.02872', '-0.007256', '0.01814', '0.00913', '0.004868', '0.0627', '0.01701', '-0.05835', '0.0877', '-0.0654', '0.002613', '0.02336', '-0.0358', '0.01052', '0.0336', '-0.012505', '0.006855', '-0.0642', '-0.02625', '0.01479', '0.01141', '-0.013916', '0.0463', '-0.0114', '0.003572', '0.0324', '0.04575', '0.05942', '0.01631', '0.0129', '0.05557', '0.006973', '0.01021', '0.1181', '0.002869', '0.04263', '-0.09015', '-0.01512', '0.01819']",,,,,,,
mondo:0013335,"tuberculin skin test reactivity, absence of","['tuberculin skin test reactivity, absence of', 'tst reactivity, absence of', 'Tst1']",,613636,,,,,,,,,,
mondo:0013336,chromosome 19p13.13 deletion syndrome,"['chromosome 19p13.13 deletion syndrome', 'Del(19)(p13.13)', '19p13.13 microdeletion syndrome', 'chromosome 19P13.13 Duplication syndrome', 'monosomy 19p13.13']",0060426,613638,357001,CN204595,,,,,,,,
mondo:0013337,"neuropathy, hereditary sensory and autonomic, type 1C","['neuropathy, hereditary sensory and autonomic, type IC', 'HSAN 1C', 'neuropathy, hereditary sensory, type 1C', 'hereditary sensory and autonomic neuropathy type IC', 'HSN 1C', 'hereditary sensory and autonomic neuropathy type 1C', 'HSAN1C']",0070157,613640,,C3150896,,,,,,,,
mondo:0013338,Charcot-Marie-Tooth disease recessive intermediate B,"['KARS Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth neuropathy recessive intermediate B', 'autosomal recessive intermediate Charcot-Marie-Tooth disease type B', 'Charcot-Marie-Tooth disease caused by mutation in KARS', 'RI-CMT type B', 'CMTRIB', 'Charcot-Marie-Tooth disease, recessive intermediate B', 'Charcot-Marie-Tooth disease recessive intermediate type B', 'Charcot-Marie-Tooth neuropathy, recessive Intermediate B', 'Charcot-Marie-Tooth disease, recessive intermediate, B', 'Charcot-Marie-Tooth disease, recessive Intermediate type B', 'RI-CMTB']",0110204,613641,254334,C3150897,"['0.1414', '0.475', '0.509', '0.05966', '0.09534', '-0.2222', '0.06586', '0.2893', '-0.526', '-0.3943', '-0.1234', '0.09314', '-0.256', '0.4607', '-0.0338', '0.0377', '-0.1256', '-0.4377', '-0.5864', '-0.6387', '0.11035', '0.3828', '0.0636', '0.8066', '0.2444', '0.07806', '0.0648', '-0.0643', '0.3608', '-0.3118', '0.2004', '-0.722', '0.5483', '0.00647', '0.1669', '-0.6177', '-0.4084', '-0.3884', '0.32', '-0.2166', '-1.433', '-0.3572', '-0.4692', '0.37', '-0.04437', '-0.3123', '0.2388', '-0.0823', '-0.301', '0.1785', '0.1', '0.3047', '-0.566', '-1.05', '-0.04364', '-0.1842', '-0.5273', '0.2573', '-0.877', '-0.2222', '-0.352', '-0.00809', '0.848', '0.718', '-0.365', '1.04', '-0.378', '0.766', '-0.543', '0.5366', '-0.841', '0.31', '0.5103', '-0.11694', '1.162', '0.4563', '-0.2084', '0.452', '-0.10693', '-0.682', '0.1636', '-0.3057', '0.5747', '0.7935', '0.1512', '-0.003548', '0.1454', '0.594', '0.577', '0.5444', '0.29', '-0.061', '0.05682', '0.304', '0.1393', '0.8047', '0.3904', '-0.8516', '0.2915', '0.5596']",,,,,,,
mondo:0013339,dilated cardiomyopathy 1GG,"['CMD1GG', 'dilated cardiomyopathy type 1GG', 'cardiomyopathy, dilated, type 1Gg', 'familial isolated dilated cardiomyopathy caused by mutation in SDHA', 'SDHA familial isolated dilated cardiomyopathy', 'cardiomyopathy, dilated, 1GG']",0110435,613642,,C3150898,,,,,,,,
mondo:0013340,"Parkinson disease 5, autosomal dominant, susceptibility to","['Parkinson disease 5, susceptibility to', 'UCHL1 young-onset Parkinson disease', 'Parkinson disease 5, autosomal dominant, susceptibility to', 'young-onset Parkinson disease caused by mutation in UCHL1', 'PARK5', 'susceptibility to autosomal dominant Parkinson disease 5']",,613643,,C3150899,,,,,,,,
mondo:0013341,methylmalonic acidemia due to transcobalamin receptor defect,"['methylmalonic acidemia, TCb1R type', 'methylmalonic acidemia, TCbIR type', 'CD320 methylmalonic acidemia', 'methylmalonic acidemia, Tcblr type', 'methylmalonic acidemia caused by mutation in CD320', 'methylmalonic aciduria due to transcobalamin receptor defect', 'methylmalonic aciduria, transient, due to transcobalamin receptor defect']",0060741,613646,280183,C3150900,"['-0.662', '0.1475', '-0.04807', '-0.09174', '-0.05063', '0.02023', '-0.4412', '0.436', '0.1576', '0.273', '-0.426', '-0.02512', '0.2311', '-0.01814', '-0.10986', '-0.4058', '0.06256', '0.1284', '-0.1094', '-0.3306', '0.1394', '-0.5415', '0.2783', '0.1428', '0.3013', '-0.011986', '0.004314', '0.006893', '-0.1105', '0.05316', '0.3164', '0.0647', '0.4133', '0.314', '-0.2737', '-0.3633', '-0.00807', '-0.2368', '0.02747', '-0.3337', '0.02031', '-0.378', '0.1941', '-0.2688', '-0.6284', '-0.1439', '0.486', '-0.1487', '0.05185', '0.1302', '0.1213', '-0.2537', '0.1334', '-0.2377', '-0.2607', '0.383', '0.4365', '-0.3748', '-0.4438', '0.485', '0.1455', '0.0371', '0.2603', '-0.09766', '0.1062', '0.1698', '0.3984', '0.3684', '-0.4502', '0.2183', '0.09576', '0.1698', '-0.459', '-0.07666', '0.2988', '0.05222', '0.2051', '-0.1641', '0.1582', '-0.02022', '0.1982', '0.0531', '0.1985', '0.3066', '-0.2078', '0.2808', '0.0635', '0.3005', '0.4736', '-0.10565', '0.3677', '0.322', '-0.463', '-0.03986', '0.4841', '0.5396', '0.3057', '-0.4822', '-0.2915', '0.2588']",,,,,,,
mondo:0013342,hereditary spastic paraplegia 48,"['autosomal recessive spastic paraplegia 48', 'autosomal recessive spastic paraplegia type 48', 'AP5Z1 hereditary spastic paraplegia', 'SPG48', 'spastic paraplegia 48, autosomal recessive', 'hereditary spastic paraplegia type 48', 'hereditary spastic paraplegia caused by mutation in AP5Z1']",0110800,613647,306511,C3150901,"['-0.0848', '0.1189', '-0.5186', '-0.122', '-0.3022', '-0.5625', '-0.7476', '-0.03128', '-0.5996', '-0.3484', '-0.516', '-0.44', '-0.323', '-0.05045', '0.75', '0.2087', '-0.3718', '-0.532', '0.2942', '-0.3982', '0.5693', '-0.4087', '0.2465', '-0.1259', '0.2417', '-0.04208', '-0.1202', '-0.06067', '0.062', '-0.1388', '0.3694', '-0.02338', '-0.0517', '-0.1097', '0.2076', '-0.3079', '-0.445', '-0.47', '-0.1621', '-0.4536', '0.3503', '-1.021', '0.1432', '0.2769', '-0.02463', '-0.5283', '-0.334', '0.3054', '-0.03854', '0.0361', '0.1936', '0.4944', '-0.7905', '-0.3582', '-0.2131', '-0.6274', '0.519', '-0.1652', '-0.5767', '0.3118', '-0.4377', '0.00631', '0.4695', '0.3562', '-0.463', '0.2272', '0.3472', '0.7393', '-0.0661', '0.961', '-0.1497', '-0.2437', '0.04', '-0.21', '0.6533', '0.1257', '-0.1738', '0.03012', '0.0305', '-0.4448', '-0.1164', '-0.11755', '0.744', '1.05', '-0.2913', '0.03815', '0.01782', '0.559', '0.29', '0.03604', '0.7217', '0.253', '0.3528', '0.406', '0.7017', '0.625', '0.4092', '0.2185', '0.347', '-0.0889']",,,,,,,
mondo:0013343,C1Q deficiency,"['C1Q deficiency', 'C1QD', 'C1q deficiency']",,613652,,C3150902,"['-0.02173', '0.0331', '-0.003483', '0.01348', '0.0187', '-0.04163', '0.01178', '0.03824', '-0.02109', '-0.03302', '0.00335', '0.005722', '0.00935', '0.012054', '-0.01991', '-0.02847', '-0.01112', '0.005928', '-0.03592', '-0.08466', '-0.004757', '-0.02312', '0.05728', '-0.01345', '0.01211', '-0.01747', '-0.01406', '-0.01475', '0.0016775', '-0.03192', '0.02438', '-0.000584', '0.04865', '0.02753', '-0.00954', '-0.01877', '-0.00903', '-0.01907', '-0.02081', '-0.03827', '0.007706', '-0.04614', '0.007362', '-0.00211', '-0.01486', '-0.03137', '0.01282', '0.02151', '0.01875', '0.03047', '-0.014', '-0.03207', '0.006668', '0.007904', '-0.02257', '-0.00606', '0.04077', '-0.004528', '-0.04553', '0.02014', '0.02515', '0.02574', '0.01816', '-0.000998', '0.01231', '0.02281', '0.02881', '0.01348', '-0.04724', '0.04437', '-0.03897', '0.00673', '-0.001189', '-0.03934', '0.0209', '0.03046', '0.018', '0.0076', '-0.01779', '-0.0176', '-0.006397', '-0.014854', '-0.00333', '0.01486', '0.03964', '-0.011185', '0.01913', '0.02242', '0.0645', '0.00979', '0.03485', '0.02556', '3.314e-05', '0.004642', '0.0798', '0.05597', '0.02441', '-0.0674', '0.012505', '0.007042']",C119990,,,,,,
mondo:0013344,"migraine, with or without aura, susceptibility to, 13","['migraine with or without aura, susceptibility to, 13', 'migraine, with or without aura, susceptibility to, 13', 'migraine, with or without aura, susceptibility to, type 13', 'migraine disorder caused by mutation in KCNK18', 'MGR13', 'KCNK18 migraine disorder', 'susceptibility to migraine with or without aura 13']",,613656,,,,,,,,,,
mondo:0013345,d-2-hydroxyglutaric aciduria 2,"['d-2-hydroxyglutaric aciduria 2', 'D2HGA2', 'D-2-hydroxyglutaric aciduria 2', 'D-2-hydroxyglutaric aciduria type 2', 'IDH2 D-2-hydroxyglutaric aciduria', 'D-2-hydroxyglutaric aciduria caused by mutation in IDH2']",0111352,613657,,C3150909,,,,,,,,
mondo:0013348,cone-rod dystrophy 15,"['retinitis pigmentosa 65', 'CDHR1 cone-rod dystrophy', 'cone-rod dystrophy 15', 'cone-rod dystrophy caused by mutation in CDHR1', 'CORD15', 'cone-rod dystrophy type 15']",0111021,613660,,C3150912,,,,,,,,
mondo:0013349,ALG11-congenital disorder of glycosylation,"['ALG11-CDG', 'congenital disorder of glycosylation, type Ip', 'CDG syndrome type Ip', 'CDG1P', 'congenital disorder of glycosylation type 1p', 'ALG11-CDG (CDG-Ip)', 'congenital disorder of glycosylation type Ip', 'CDG-Ip', 'carbohydrate deficient glycoprotein syndrome type Ip']",0080567,613661,280071,C3150913,"['-0.496', '0.193', '0.2247', '-0.434', '0.1428', '-0.1836', '-0.2842', '0.0355', '-0.4927', '-0.1144', '-0.1499', '-0.1578', '0.11053', '0.009056', '-0.744', '0.0982', '0.2754', '-0.2325', '-0.299', '-0.753', '0.4045', '-0.2827', '-0.1439', '0.000278', '0.3174', '0.0346', '-0.1433', '0.03177', '0.1548', '-0.1223', '0.6055', '0.1421', '0.6724', '0.2637', '-0.0978', '0.2861', '-0.3638', '0.256', '-0.01576', '-0.383', '-0.363', '-0.0746', '0.2125', '-0.08545', '-0.1954', '-0.02393', '0.337', '-0.02055', '0.1785', '0.3433', '-0.6226', '0.1465', '0.05527', '0.3218', '-0.4678', '-0.04178', '-0.03577', '0.427', '-0.26', '0.2067', '0.3154', '0.1097', '0.1476', '-0.2067', '0.2847', '0.0989', '0.1979', '0.1635', '-0.4387', '0.2876', '-0.4136', '0.6514', '0.1858', '0.0798', '-0.02684', '0.3018', '0.8013', '-0.423', '-0.04538', '0.1549', '0.1381', '0.03326', '0.04697', '0.1575', '0.08484', '0.2188', '-0.1392', '0.662', '0.3928', '0.3542', '-0.1875', '0.631', '0.3267', '0.1522', '0.2512', '0.5825', '0.4727', '-0.10394', '0.4714', '0.4595']",,,,,,,
mondo:0013350,mitochondrial DNA depletion syndrome 4b,"['MTDPS4B', 'mitochondrial neurogastrointestinal encephalopathy syndrome, Polg-related', 'mitochondrial DNA depletion syndrome 4B (MNGIE type)', 'Mngie, Polg-related', 'mitochondrial DNA depletion syndrome type 4b']",0080123,613662,298,C3150914,,,,,,,,
mondo:0013351,infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly,"['microcephaly, postnatal progressive, with seizures and brain atrophy', 'postnatal progressive microcephaly, seizures, and brain atrophy']",0111262,613668,402364,C3150921,"['-0.02469', '0.394', '0.4058', '0.08185', '0.1544', '-0.2556', '0.1667', '0.6895', '-1.327', '-0.2683', '-0.0899', '-0.0946', '0.2375', '0.322', '0.5527', '-0.428', '0.685', '0.1935', '-0.528', '-1.086', '0.005455', '0.08685', '0.0878', '-0.1364', '0.1553', '0.1354', '-0.2097', '0.1262', '0.1185', '-0.3125', '-0.2305', '-0.2079', '0.692', '-0.1711', '-0.2764', '0.97', '-0.6196', '-0.1344', '-0.0897', '-0.2394', '0.1642', '-0.05835', '-0.6426', '-0.2727', '0.1373', '-0.4536', '0.826', '0.175', '-0.1925', '-0.2357', '0.1553', '-0.6206', '-0.0869', '-0.521', '-0.1539', '0.1727', '-0.835', '0.409', '-0.66', '0.3813', '0.1835', '0.3618', '0.4336', '0.463', '-0.3093', '-0.2279', '0.649', '0.05344', '-0.9336', '0.1796', '-0.6094', '1.156', '0.3633', '-1.134', '-0.10724', '0.4177', '0.511', '-0.3853', '-0.1794', '0.1224', '-0.5786', '0.9927', '-0.03177', '0.7886', '-0.0003476', '-0.461', '0.3262', '-0.4011', '0.935', '0.4094', '-0.001331', '0.2352', '-0.359', '0.1326', '-0.4055', '0.5083', '1.0625', '-0.428', '0.6753', '-0.6846']",,,,,,,
mondo:0013352,intellectual disability-severe speech delay-mild dysmorphism syndrome,"['mental retardation with language impairment and with or without autistic features', 'FOXP1 related global developmental delay, intellectual disability and speech defects', 'intellectual disability with language impairment and with or without autistic features']",0111331,613670,391372,CN204965,"['-0.4023', '0.06586', '0.3042', '-0.6', '-0.4075', '-0.3108', '-0.06635', '0.5103', '-0.875', '-0.4514', '0.1256', '-0.09784', '0.3362', '0.0209', '0.0654', '0.09143', '0.1458', '-0.3723', '-0.2294', '-0.598', '0.10034', '0.4072', '-0.2466', '0.03842', '0.7393', '-0.2659', '-0.1587', '0.12024', '0.577', '-0.02473', '0.324', '-0.387', '0.358', '0.1326', '0.256', '-0.1749', '-0.2295', '-0.1102', '-0.1584', '-0.557', '0.4043', '-0.149', '-0.2534', '0.01945', '0.1478', '-0.2136', '0.0697', '0.1114', '-0.2815', '0.1852', '-0.506', '0.1886', '-0.7104', '0.335', '-0.025', '-0.0277', '-0.06006', '0.05222', '0.0138', '0.2922', '-0.02373', '0.1897', '0.1056', '0.0353', '0.0933', '0.1029', '-0.08453', '0.1643', '-0.2297', '0.7627', '-0.567', '0.4622', '-0.4192', '0.1097', '-0.325', '0.4075', '0.221', '-0.1901', '-0.337', '0.05542', '0.2515', '-0.2822', '-0.0501', '0.4475', '0.0964', '0.00667', '-0.4395', '0.6265', '0.4402', '0.6836', '-0.06186', '0.6577', '0.1145', '0.176', '0.5933', '0.195', '0.2325', '-0.622', '0.6343', '0.02486']",,1001500,,,,,
mondo:0013353,"intellectual disability, anterior maxillary protrusion, and strabismus","['MRAMS', 'intellectual disability, anterior maxillary protrusion, and strabismus', 'mental retardation, anterior maxillary protrusion, and strabismus']",,613671,562559,C3150924,,,,,,,,
mondo:0013354,spastic ataxia 4,"['autosomal recessive spastic ataxia - optic atrophy - dysarthria', 'autosomal recessive spastic ataxia-optic atrophy-dysarthria syndrome', 'autosomal recessive spastic ataxia 4', 'spastic ataxia type 4', 'MTPAP autosomal recessive spastic ataxia', 'spastic ataxia 4, autosomal recessive', 'autosomal recessive spastic ataxia type 4', 'autosomal recessive spastic ataxia caused by mutation in MTPAP', 'SPAX4']",0050943,613672,254343,CN230090,"['-0.0822', '-0.2092', '-0.1688', '0.1991', '-0.3335', '-1.023', '-0.004368', '-0.1818', '-0.8203', '-1.0205', '0.1804', '0.2002', '-0.221', '0.2693', '0.6206', '-0.2347', '-0.2024', '-0.2253', '0.1885', '-0.756', '-0.05423', '-0.2776', '0.2064', '-0.61', '0.4458', '-0.4817', '-0.3892', '0.2181', '-0.0398', '-0.973', '0.317', '0.558', '-0.556', '-0.11017', '0.417', '0.1292', '-0.2433', '0.2065', '0.4893', '0.4607', '0.279', '0.1444', '-0.571', '0.482', '0.379', '-0.6855', '0.00852', '0.367', '0.4248', '-0.02527', '-0.2693', '0.10254', '-0.03278', '-0.2129', '-0.1699', '-1.009', '0.47', '0.559', '-0.09875', '0.5337', '-0.379', '0.3271', '0.3916', '-0.23', '-0.48', '0.4868', '0.3838', '0.6895', '-0.5137', '0.4434', '0.656', '0.3523', '-0.032', '-0.659', '0.7944', '0.3413', '0.0485', '0.2632', '-0.005005', '0.552', '-0.226', '-0.804', '0.4546', '0.843', '-0.1198', '-0.8364', '0.1803', '-0.2375', '0.5615', '0.4265', '0.4868', '0.4346', '0.1346', '0.0816', '1.129', '0.979', '0.2615', '0.3865', '-0.5586', '-0.175']",,,,,G11.4,,
mondo:0013355,congenital dyserythropoietic anemia type 4,"['anemia, congenital dyserythropoietic, type IV', 'CDA type 4', 'congenital dyserythropoietic anaemia due to KLF1 mutation', 'dyserythropoietic anemia, congenital, type IV', 'CDA, type 4', 'CDA due to KLF1 mutation', 'congenital dyserythropoietic anemia due to KLF1 mutation', 'CDAN4', 'congenital dyserythropoietic anemia type 4', 'anemia, congenital dyserythropoietic, type 4', 'CDA IV', 'CDA type IV']",0111400,613673,293825,C3150926,"['-0.6353', '0.3628', '-0.169', '0.2067', '0.533', '0.1703', '-0.4768', '0.497', '-0.0273', '-0.647', '0.5283', '0.000899', '0.537', '0.2009', '-1.203', '0.149', '-0.73', '0.1183', '-0.581', '-0.53', '-0.05685', '-0.2152', '0.2075', '-0.4001', '0.807', '-0.0898', '-0.10516', '-0.2284', '0.6167', '0.3328', '0.13', '0.2394', '0.663', '0.4368', '0.4211', '-0.624', '-0.74', '-0.6987', '0.3252', '-0.1333', '-0.76', '0.3513', '0.07214', '-0.4512', '-0.5757', '-0.666', '0.1779', '0.2666', '0.4165', '-0.559', '0.5557', '0.1489', '0.6187', '-0.0749', '0.6113', '-0.7964', '0.10205', '0.3682', '-0.928', '0.0672', '0.1004', '0.2096', '-0.1371', '-0.305', '-0.0009665', '0.1743', '0.1716', '0.6846', '-0.3542', '1.04', '0.533', '-0.19', '-0.2832', '-0.4832', '0.1981', '1.146', '0.2722', '0.284', '0.01174', '0.4644', '0.3284', '-0.1605', '0.1184', '0.005184', '0.375', '-0.3792', '-0.5103', '0.4087', '0.829', '-0.2124', '0.6074', '0.357', '-0.1713', '-0.0742', '0.804', '0.979', '0.2439', '0.10516', '0.3499', '-0.66']",,,,,,,
mondo:0013356,vesicoureteral reflux 3,"['SOX17 vesicoureteral reflux (disease)', 'vesicoureteral reflux 3', 'vesicoureteral reflux type 3', 'VUR3']",,613674,,C3150927,,,,,,,,
mondo:0013357,"chromosome 17q11.2 deletion syndrome, 1.4Mb","['Van Asperen syndrome', 'overgrowth-macrocephaly-facial dysmorphism syndrome', '17q11 microdeletion syndrome', 'neurofibromatosis type 1 microdeletion syndrome', 'neurofibromatosis 1 microdeletion syndrome', 'Del(17)(q11)', 'MMFD', 'chromosome 17q11.2 deletion syndrome', 'monosomy 17q11', 'chromosome 17q11.2 deletion syndrome, 1.4-MB', 'NF1 microdeletion syndrome', 'RNF135-related overgrowth syndrome', 'NF1 microduplication syndrome', 'macrocephaly, macrosomia, and facial dysmorphism syndrome']",0060403,613675,97685,C3280095,,,,C563524,,,,
mondo:0013358,Seckel syndrome 4,"['Seckel syndrome caused by mutation in CENPJ', 'SCKL4', 'Seckel syndrome 4', 'CENPJ Seckel syndrome', 'Seckel syndrome type 4']",0070010,613676,,C3888212,,,,,,,,
mondo:0013359,familial hyperaldosteronism type III,"['FH3', 'FH-III', 'hyperaldosteronism, familial, type III', 'FH 3', 'FH III', 'hyperaldosteronism, familial, type 3', 'HALD3', 'familial hyperaldosteronism type 3']",,613677,251274,C3838758,"['-0.5684', '-0.1309', '-0.428', '-0.3684', '-0.501', '-0.1691', '-0.2057', '0.3613', '-0.3325', '-0.379', '-0.3953', '-0.2228', '0.3381', '0.1589', '-0.2212', '-0.1544', '0.1398', '0.01061', '0.5073', '-0.732', '-0.1573', '-0.302', '0.1589', '0.08307', '-0.10645', '0.2358', '0.251', '-0.1884', '0.1381', '-0.198', '0.07874', '0.2161', '0.9717', '0.09924', '-0.785', '-0.1885', '-0.433', '0.2216', '0.1676', '-0.06', '-0.1533', '-0.5884', '0.3606', '-0.888', '0.3262', '0.4204', '0.00947', '0.1315', '-0.01643', '-0.1039', '0.12445', '0.1205', '0.542', '-0.5654', '-0.3386', '0.3643', '-0.1521', '-0.874', '-0.4329', '0.973', '-0.05222', '0.10864', '0.1173', '-0.7554', '-0.2079', '0.11224', '0.277', '0.5303', '-0.506', '0.1782', '-0.2883', '0.07245', '0.3225', '-0.5845', '0.4536', '0.3906', '-0.646', '0.0755', '-0.1049', '0.3506', '0.447', '0.5684', '-0.02394', '0.0967', '0.1035', '0.533', '0.1802', '-0.1537', '0.437', '0.4978', '0.299', '0.3223', '0.5156', '-0.2089', '0.7705', '0.198', '0.629', '-0.5527', '-0.3057', '0.304']",,,,,,,
mondo:0013360,"brachyolmia, Maroteaux type","['BCYM2', 'brachyolmia type 2', 'brachyolmia, Maroteaux type']",,613678,93302,,,,,,,,,
mondo:0013361,congenital prothrombin deficiency,"['Dysprothrombinemia', 'prothrombin deficiency', 'hereditary prothrombin deficiency', 'prothrombin deficiency, congenital', 'factor 2 deficiency', 'hypoprothrombinemia', 'factor II deficiency', 'congenital factor II deficiency']",2235,613679,325,C0020640,"['-0.4421', '-0.09326', '-0.9165', '-0.472', '-0.1636', '0.02211', '-0.2776', '0.4788', '-0.1781', '0.1654', '-0.3555', '0.1926', '0.266', '0.08124', '-0.339', '0.2285', '0.0692', '0.1812', '-0.3518', '-0.774', '-0.4434', '-0.2253', '1.169', '-0.1472', '0.007694', '0.0843', '-0.2008', '0.428', '0.4517', '-0.3816', '0.1666', '0.1388', '0.2937', '0.5366', '-0.5825', '-0.3013', '-0.2057', '-0.3525', '0.4158', '-0.1687', '0.2393', '-0.3877', '0.3745', '-0.1533', '0.4868', '0.1443', '-0.013016', '0.375', '0.4812', '0.2242', '0.8096', '-0.721', '0.3193', '0.0845', '-0.3901', '0.3013', '0.0761', '0.1241', '-0.729', '0.01091', '-0.223', '0.1195', '0.3284', '-0.279', '0.1956', '0.1323', '0.4011', '0.2155', '-0.303', '0.0291', '-0.5947', '-0.4414', '-0.609', '-0.753', '1.123', '0.0517', '0.8286', '0.00405', '0.3013', '-0.261', '-0.5522', '-0.0575', '0.06824', '0.1528', '0.1277', '0.3533', '0.1205', '0.2993', '0.1186', '-0.792', '0.05423', '1.179', '0.5977', '0.1084', '0.7515', '0.8633', '0.4878', '-0.52', '-0.1514', '0.02219']",C131737,,D007020,286.3,,,
mondo:0013362,THOC6-related developmental delay-microcephaly-facial dysmorphism syndrome,"['Beaulieu-Boycott-Innes syndrome', 'BBIS', 'BEAULIEU-BOYCOTT-Innes syndrome', 'microcephaly, mental retardation, and distinctive facies, with Cardiac and genitourinary malformations', 'microcephaly, intellectual disability, and distinctive facies, with Cardiac and genitourinary malformations']",,613680,363444,C3150939,"['0.4268', '0.2484', '0.431', '-0.216', '0.423', '-0.0558', '0.5254', '0.8906', '-0.6797', '-0.2817', '0.2576', '-0.2668', '0.6387', '0.3516', '-0.1007', '0.1277', '0.3328', '-0.2722', '-0.7607', '-0.7197', '0.0544', '0.02791', '0.1819', '-0.00986', '0.262', '-0.1111', '-0.2188', '0.4526', '0.8076', '-0.3604', '0.01906', '-0.2542', '0.833', '-0.2896', '-0.1121', '0.2761', '-0.6104', '-0.2544', '-0.3594', '-0.0757', '0.3054', '0.2878', '-0.2333', '-0.7036', '0.07794', '-0.1123', '0.536', '0.134', '-0.482', '-0.1558', '-0.02934', '-0.587', '-0.0768', '-0.432', '-0.3416', '0.1368', '-0.9346', '0.4814', '-0.182', '-0.1394', '0.1393', '0.4578', '0.1567', '0.241', '-0.1687', '-0.2588', '0.2676', '-0.01418', '-0.9673', '-0.1005', '-0.5728', '0.7705', '-0.042', '-0.4119', '0.1588', '0.4705', '0.847', '-0.4778', '-0.633', '0.3042', '-0.1361', '0.895', '0.2373', '0.5615', '-0.1832', '0.1442', '0.1919', '-0.4163', '0.622', '0.6797', '-0.1395', '0.2815', '-0.1156', '0.1538', '0.3625', '-0.08813', '1.015', '-0.04276', '0.903', '-0.4094']",,,,,,,
mondo:0013363,chromosome 2q31.1 duplication syndrome,"['mesomelic dysplasia, 2Q31.1 Duplication-related', '2q31.1 microduplication syndrome', 'chromosome 2q31.1 duplication syndrome', 'trisomy 2q31.1', 'dup(2)(q31.1)']",0060458,613681,294026,CN203162,,,,,,,,
mondo:0013364,Rubinstein-Taybi syndrome due to EP300 haploinsufficiency,"['Rubinstein-Taybi syndrome 2', 'Rubinstein-Taybi syndrome type 2', 'RSTS2', 'EP300 Rubinstein-Taybi syndrome']",,613684,353284,C3150941,"['-0.4102', '0.2842', '0.1147', '-0.0761', '0.06384', '-0.412', '-0.11914', '0.2776', '-0.4163', '-0.1991', '0.05435', '0.1256', '0.0354', '-0.08307', '0.376', '-0.0982', '0.02612', '0.003883', '-0.2385', '-0.32', '0.2275', '-0.0206', '0.04932', '-0.003601', '0.2732', '0.1704', '-0.2124', '0.04697', '0.04852', '-0.00624', '0.0854', '0.1816', '0.3804', '0.1813', '0.3005', '-0.297', '0.03494', '-0.1713', '0.03592', '-0.3972', '0.257', '-0.2854', '-0.07043', '-0.0724', '-0.0484', '-0.2898', '-0.02014', '0.115', '-0.02673', '-0.08777', '-0.1532', '-0.05536', '-0.166', '0.108', '-0.2045', '-0.08813', '0.4265', '-0.0015335', '-0.1162', '0.107', '0.0342', '0.23', '0.1466', '0.06854', '0.263', '0.07556', '0.1165', '0.005344', '-0.375', '0.1348', '-0.4126', '0.0595', '0.1327', '-0.1364', '0.0779', '-0.1841', '0.001348', '0.1088', '-0.1309', '0.0909', '0.1555', '0.0836', '-0.151', '0.1543', '-0.03885', '-0.228', '0.1824', '0.5913', '0.3958', '0.307', '0.1465', '0.014175', '0.01837', '-0.2502', '0.5083', '0.1696', '0.2969', '-0.547', '0.236', '0.006153']",C153291,,,,,,
mondo:0013365,autosomal recessive nonsyndromic hearing loss 83,"['DFNB83', 'autosomal recessive deafness 83', 'deafness, autosomal recessive 83', 'autosomal recessive nonsyndromic deafness type 83', 'autosomal recessive nonsyndromic deafness 83']",0110528,613685,,,,,,,,,,
mondo:0013366,"spondylocostal dysostosis 4, autosomal recessive","['SCDO4', 'autosomal recessive spondylocostal dysostosis caused by mutation in Hes7', 'spondylocostal dysostosis 4', 'spondylocostal dysostosis 4, autosomal recessive', 'Hes7 autosomal recessive spondylocostal dysostosis', 'HES7 autosomal recessive spondylocostal dysostosis']",0112364,613686,,C3150942,,,,,,,,
mondo:0013367,long QT syndrome 2,"['long QT syndrome type 2', 'LQT2', 'long QT syndrome 1/2, digenic', 'long QT syndrome 2/5, digenic', 'long QT syndrome 2/9, digenic', 'long QT syndrome 2/3, digenic', 'long QT syndrome 2', 'Long QT syndrome, acquired, reduced susceptibility to', 'long QT syndrome 2, acquired, susceptibility to']",0110645,613688,101016,C3150943,,C137957,,C563614,,,,
mondo:0013368,mammary-digital-nail syndrome,"['mammary-digital-nail syndrome', 'MDN syndrome', 'onycho-digito-mammary syndrome', 'MDNS']",,613689,238744,C3150946,,,,,,,,
mondo:0013369,hypertrophic cardiomyopathy 7,"['TNNI3 hypertrophic cardiomyopathy', 'cardiomyopathy, familial hypertrophic, type 7', 'cardiomyopathy, hypertrophic, 7', 'cardiomyopathy, familial hypertrophic 7', 'hypertrophic cardiomyopathy type 7', 'cardiomyopathy, familial hypertrophic, 7', 'hypertrophic cardiomyopathy caused by mutation in TNNI3', 'CMH7']",0110313,613690,,C1860752,,,,,,,,
mondo:0013370,long QT syndrome 6,"['long QT syndrome 6, acquired, susceptibility to', 'long QT syndrome caused by mutation in KCNE2', 'long QT syndrome 6', 'KCNE2 long QT syndrome', 'long QT syndrome 3/6, digenic', 'long QT syndrome type 6', 'LQT6']",0110648,613693,101016,C3150953,,,,C566333,,,,
mondo:0013371,dilated cardiomyopathy 1U,"['PSEN1 familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 1U', 'cardiomyopathy, dilated, 1U', 'CMD1U', 'familial isolated dilated cardiomyopathy caused by mutation in PSEN1', 'cardiomyopathy, dilated, type 1U']",0110455,613694,,C3160720,,,,C566296,,,,
mondo:0013372,long QT syndrome 5,"['long QT syndrome type 5', 'long QT syndrome 2/5, digenic', 'long QT syndrome 5, acquired, susceptibility to', 'long QT syndrome caused by mutation in KCNE1', 'KCNE1 long QT syndrome', 'LQT5', 'long QT syndrome 5']",0110647,613695,101016,C1867904,,C172094,,C566766,,,,
mondo:0013373,dilated cardiomyopathy 1V,"['familial isolated dilated cardiomyopathy caused by mutation in PSEN2', 'CMD1V', 'cardiomyopathy, dilated, type 1V', 'cardiomyopathy, dilated, 1V', 'dilated cardiomyopathy type 1V', 'PSEN2 familial isolated dilated cardiomyopathy']",0110427,613697,,C3150958,,,,C566856,,,,
mondo:0013374,supernumerary der(22)t(8;22) syndrome,"['supernumerary der(22)t(8;22) syndrome', 'supernumerary der(22)t(8-22) syndrome']",,613700,,C3150966,,,,,,,,
mondo:0013375,"Klippel-Feil syndrome 3, autosomal dominant","['GDF3 isolated Klippel-Feil syndrome', 'Klippel-FEIL syndrome 3, autosomal dominant', 'Klippel-Feil syndrome 3, autosomal dominant', 'KFS3', 'isolated Klippel-Feil syndrome caused by mutation in GDF3']",0080591,613702,,C3150967,,,,,,,,
mondo:0013376,"microphthalmia, isolated, with coloboma 6","['microphthalmia with coloboma 6', 'microphthalmia, isolated, with coloboma type 6', 'microphthalmia, isolated, with coloboma 6', 'MCOPCB6', 'microphthalmia with coloboma 6, digenic']",,613703,,C3150968,,,,,,,,
mondo:0013377,isolated microphthalmia 7,"['isolated microphthalmia caused by mutation in GDF3', 'microphthalmia, isolated type 7', 'microphthalmia, isolated 7', 'isolated microphthalmia type 7', 'GDF3 isolated microphthalmia', 'MCOP7']",0060838,613704,,C3150969,,,,,,,,
mondo:0013378,orofacial cleft 10,"['orofacial cleft 10, isolated cases', 'SUMO1 orofacial cleft', 'cleft lip with or without cleft palate, nonsyndromic, 10', 'OFC10', 'orofacial cleft 10', 'orofacial cleft type 10', 'orofacial cleft caused by mutation in SUMO1']",0080403,613705,,,,,,C566605,,,,
mondo:0013379,Noonan syndrome 7,"['Noonan syndrome type 7', 'Noonan syndrome 7', 'BRAF Noonan syndrome', 'Noonan syndrome caused by mutation in BRAF', 'NS7']",0060585,613706,,C3150970,,C176935,,,,,,
mondo:0013380,LEOPARD syndrome 3,"['leopard syndrome 3', 'Leopard syndrome type 3', 'Noonan syndrome with multiple lentigines caused by mutation in BRAF', 'LPRD3', 'BRAF Noonan syndrome with multiple lentigines', 'LEOPARD syndrome 3']",0080550,613707,,C3150971,,,,,,,,
mondo:0013381,"neuropathy, hereditary sensory, type 1D","['hereditary sensory neuropathy type 1D', 'hereditary sensory neuropathy type ID', 'HSN1D', 'neuropathy, hereditary sensory, type ID']",0070156,613708,,C3150972,,,,,,,,
mondo:0013382,progressive demyelinating neuropathy with bilateral striatal necrosis,"['progressive polyneuropathy with bilateral striatal necrosis', 'THMD4', 'bilateral striatal Degeneration and progressive polyneuropathy', 'thiamine metabolism dysfunction syndrome 4 (progressive polyneuropathy type)', 'striatal Necrosis, bilateral, and progressive polyneuropathy', 'thiamine metabolism dysfunction syndrome 4 (bilateral striatal degeneration and progressive polyneuropathy type)']",,613710,217396,C3150973,"['-0.77', '-0.1451', '0.0865', '0.11755', '0.03137', '-0.8228', '-0.0901', '0.2698', '-0.534', '0.261', '-0.4812', '-0.05447', '0.0004249', '-0.2064', '0.1504', '-0.2313', '0.0961', '-0.0764', '-0.0577', '-0.972', '0.3923', '-0.15', '-0.000552', '0.0991', '0.1866', '0.01855', '0.4175', '-0.05112', '-0.3508', '-0.3362', '-0.329', '0.154', '0.2009', '0.12054', '-0.1465', '-0.3477', '-0.1567', '-0.1943', '-0.1415', '-0.11084', '-0.3718', '-0.677', '-0.2554', '0.10364', '-0.09467', '-0.11743', '-0.294', '0.255', '-0.137', '0.402', '-0.3096', '0.2006', '0.2451', '-0.06213', '-0.10736', '-0.675', '0.6274', '-0.2805', '-0.4202', '0.3396', '0.007385', '-0.1322', '0.2844', '-0.1425', '-0.3728', '-0.03528', '0.4507', '0.718', '-0.2964', '0.1825', '-0.2903', '-0.1686', '-0.05884', '-0.03047', '0.2986', '0.0747', '0.3418', '0.647', '0.2622', '-0.1609', '0.0816', '-0.3228', '0.2766', '0.6997', '0.0656', '-0.2046', '-0.2068', '0.4507', '-0.07526', '0.0531', '0.3987', '0.2379', '0.2019', '-0.10144', '0.2008', '0.55', '1.013', '-0.4736', '-0.4941', '0.3555']",,,,,,,
mondo:0013383,"Hirschsprung disease, susceptibility to, 3","['Hirschsprung disease modifier', 'Hirschsprung disease, susceptibility to, type 3', 'Hirschsprung disease type 3', 'susceptibility to Hirschsprung disease 3', 'Hirschsprung disease, susceptibility to, 3', 'Hirschsprung disease caused by mutation in GDNF', 'GDNF Hirschsprung disease', 'HSCR3']",,613711,,C2931739,,,,C538121,,,,
mondo:0013384,"Hirschsprung disease, susceptibility to, 4","['EDN3 Hirschsprung disease', 'susceptibility to Hirschsprung disease 4', 'Hirschsprung disease, susceptibility to, 4', 'Hirschsprung disease, susceptibility to, type 4', 'HSCR4', 'Hirschsprung disease caused by mutation in EDN3']",,613712,,,,,,,,,,
mondo:0013385,Treacher Collins syndrome 2,"['Treacher Collins syndrome type 2', 'Treacher-Collins syndrome caused by mutation in POLR1D', 'Treacher Collins syndrome 2', 'TCS2', 'POLR1D Treacher-Collins syndrome', 'TREACHER COLLINS syndrome 2']",0080790,613717,,C3150983,,,,,,,,
mondo:0013386,autosomal recessive nonsyndromic hearing loss 74,"['DFNB74', 'autosomal recessive nonsyndromic deafness caused by mutation in MSRB3', 'deafness, autosomal recessive 74', 'deafness, autosomal recessive type 74', 'autosomal recessive deafness 74', 'MSRB3 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness 74', 'autosomal recessive nonsyndromic deafness type 74']",0110523,613718,,C2239351,,,,,,,,
mondo:0013387,"developmental and epileptic encephalopathy, 7","['KCNQ2-related neonatal epileptic encephalopathy', 'KCNQ2-related epileptic encephalopathy', 'epileptic encephalopathy, early infantile, type 7', 'EIEE7', 'KCNQ2-related disorders', 'developmental and epileptic encephalopathy 7', 'epileptic encephalopathy, early infantile, 7', 'KCNQ2-NEE', 'DEE7']",0080462,613720,439218,C3150986,,,,,,,,
mondo:0013388,"developmental and epileptic encephalopathy, 11","['early infantile epileptic encephalopathy caused by mutation in SCN2A', 'epileptic encephalopathy, early infantile, 11', 'DEE11', 'epileptic encephalopathy, early infantile, type 11', 'SCN2A early infantile epileptic encephalopathy', 'EIEE11', 'developmental and epileptic encephalopathy 11']",0080421,613721,,C3150987,,,,,,,,
mondo:0013389,"developmental and epileptic encephalopathy, 12","['DEE12', 'PLCB1 early infantile epileptic encephalopathy', 'developmental and epileptic encephalopathy 12', 'EIEE12', 'early infantile epileptic encephalopathy caused by mutation in PLCB1', 'epileptic encephalopathy, early infantile, 12', 'early infantile epileptic encephalopathy 12', 'epileptic encephalopathy, early infantile, type 12']",0080459,613722,,C3150988,,,,,,,,
mondo:0013390,autosomal recessive limb-girdle muscular dystrophy type 2Q,"['muscular dystrophy, limb-girdle, autosomal recessive 17', 'autosomal recessive limb-girdle muscular dystrophy due to plectin deficiency', 'limb-girdle muscular dystrophy type 2Q', 'LGMD2Q', 'muscular dystrophy, limb-girdle, type 2Q']",0110285,613723,254361,C3150989,"['-0.2869', '-0.8594', '-0.4836', '-0.2507', '0.3384', '-1.343', '0.1034', '0.736', '-1.648', '-0.7144', '0.1279', '0.5776', '-0.2563', '0.851', '0.2568', '0.186', '-0.9785', '-0.6777', '-0.4268', '-0.902', '-0.1364', '0.1594', '0.409', '0.723', '-0.01768', '0.013145', '-0.506', '-1.046', '0.144', '-0.5015', '0.838', '-0.1382', '0.537', '-0.001377', '0.2327', '-0.03876', '-0.5117', '0.2424', '0.03455', '-0.2198', '0.1194', '-0.11664', '-0.3403', '0.3193', '-0.0369', '0.3464', '0.1526', '0.634', '-0.1313', '0.5024', '0.549', '-0.3025', '0.4417', '-0.78', '-0.03001', '-0.76', '0.4956', '0.953', '-0.1244', '0.1841', '0.1805', '0.004776', '-0.1454', '0.02884', '-0.1144', '0.02202', '0.1736', '0.511', '-0.236', '0.01738', '-0.2659', '0.4946', '0.0895', '-0.1826', '0.7437', '0.4001', '-0.0346', '0.2568', '0.1803', '0.1882', '0.2766', '0.02094', '-0.11896', '0.3806', '-0.07745', '0.1509', '-0.11676', '-0.5493', '0.6455', '0.3342', '-0.2778', '0.2915', '0.497', '1.065', '0.189', '0.2067', '0.291', '-0.4275', '0.0798', '-0.2407']",,,,,,,
mondo:0013391,sterol carrier protein 2 deficiency,"['leukoencephalopathy - dystonia - motor neuropathy', 'leukoencephalopathy-dystonia-motor neuropathy syndrome', 'leukoencephalopathy with dystonia and motor neuropathy', 'LKDMN', 'SCP2 deficiency', 'sterol carrier protein 2 deficiency']",,613724,163684,C3150990,"['0.4058', '0.1407', '0.1598', '-0.4548', '-0.251', '-1.112', '0.4885', '0.04083', '-0.77', '0.2378', '0.7456', '0.648', '-0.538', '0.10815', '0.7783', '0.4102', '-0.02982', '-0.6313', '-0.666', '-0.9463', '-0.1907', '0.02454', '-0.317', '-0.0967', '-0.3694', '0.1685', '-0.04745', '0.03766', '0.03305', '0.11456', '0.2893', '0.5913', '0.989', '-0.629', '0.694', '0.00703', '0.569', '-0.2512', '0.517', '-0.588', '0.7524', '-0.05774', '-0.463', '0.41', '0.534', '-0.1215', '-0.1976', '0.4727', '0.2007', '0.2168', '0.2512', '0.19', '0.0919', '-0.03516', '0.2316', '0.2822', '0.2722', '0.644', '-0.12335', '-0.1625', '-0.7495', '-0.4377', '-0.09467', '-0.3027', '-1.225', '0.6216', '0.3853', '0.7593', '-0.09375', '0.499', '-0.2817', '0.1832', '0.1385', '-0.2705', '0.2085', '0.3003', '0.8394', '0.1803', '-0.0715', '-0.3594', '-0.262', '0.1771', '0.4001', '0.4912', '0.604', '-0.02115', '-0.0445', '0.5205', '1.594', '-0.3428', '0.6465', '0.1158', '0.5474', '0.1748', '1.145', '-0.1405', '-0.622', '0.1617', '0.2883', '-0.4312']",,,,,,,
mondo:0013392,autosomal recessive spinocerebellar ataxia 10,"['SCAR10', 'autosomal recessive spinocerebellar ataxia type 10', 'autosomal recessive cerebellar ataxia caused by mutation in ANO10', 'spinocerebellar ataxia, autosomal recessive type 10', 'spinocerebellar ataxia, autosomal recessive 10', 'ANO10 autosomal recessive cerebellar ataxia', 'adult-onset autosomal recessive cerebellar ataxia']",0050999,613728,284289,C3150998,"['-0.3127', '-0.2238', '-0.05765', '0.1881', '-0.3047', '-1.076', '0.0723', '-0.06244', '-0.636', '-0.682', '0.1407', '0.16', '-0.2092', '0.2401', '0.3958', '-0.3162', '-0.1726', '-0.2008', '0.1672', '-0.9805', '0.03656', '-0.329', '0.04266', '-0.4956', '0.4683', '-0.49', '-0.2532', '0.3442', '-0.1782', '-0.9277', '0.001812', '0.4807', '-0.6235', '-0.22', '0.4814', '0.1351', '-0.2754', '0.1454', '0.5303', '0.4124', '0.331', '0.2457', '-0.3955', '0.4072', '0.4429', '-0.661', '0.1676', '0.469', '0.537', '-0.0832', '-0.0806', '0.1975', '-0.08954', '-0.4358', '-0.1119', '-0.8984', '0.3396', '0.58', '-0.2612', '0.3142', '-0.539', '0.3215', '0.3499', '-0.10144', '-0.5073', '0.763', '0.286', '0.605', '-0.54', '0.4556', '0.769', '0.6113', '0.05786', '-0.785', '0.5996', '0.2067', '0.2766', '0.381', '0.2201', '0.503', '-0.4539', '-1.006', '0.4766', '0.841', '-0.357', '-0.515', '0.1434', '-0.04593', '0.526', '0.4104', '0.5405', '0.4204', '0.065', '0.1659', '0.9395', '1.052', '0.4321', '0.4302', '-0.4285', '-0.1718']",,,,,,,
mondo:0013393,distal 7q11.23 microdeletion syndrome,"['chromosome 7q11.23 deletion syndrome, distal, 1.2mb', 'distal chromosome 7Q11.23 deletion syndrome', 'chromosome 7q11.23 deletion syndrome, distal, 1.2-MB', 'distal del(7)(q11.23)', 'distal monosomy 7q11.23']",,613729,254351,C3150999,,,,,,,,
mondo:0013394,porencephaly-microcephaly-bilateral congenital cataract syndrome,"['HDBSCC', 'hemorrhagic destruction of the brain, subependymal calcification, and cataracts']",,613730,306547,C3151000,"['-0.004223', '0.4395', '0.3496', '0.04816', '0.0868', '-0.01813', '0.093', '0.514', '-0.969', '-0.317', '-0.10156', '-0.1407', '0.2035', '0.5166', '0.53', '-0.1819', '0.516', '0.353', '-0.536', '-1.154', '-0.02292', '-0.02261', '0.0401', '-0.08813', '0.3767', '0.0701', '-0.1842', '0.4617', '0.0774', '-0.09326', '-0.2113', '-0.5254', '0.4358', '-0.1847', '-0.1871', '0.879', '-0.5894', '-0.1732', '-0.08075', '-0.2905', '-0.0756', '0.4805', '-0.639', '-0.3513', '0.1862', '-0.272', '0.8096', '0.1431', '0.05777', '-0.2043', '0.3157', '-0.3005', '-0.012085', '-0.1938', '-0.1157', '0.2395', '-0.6694', '0.5186', '-0.72', '0.11176', '0.3462', '0.324', '0.4182', '0.325', '-0.2236', '0.113', '0.516', '0.134', '-1.2', '0.232', '-0.7183', '1.002', '0.3704', '-0.862', '0.1602', '0.2346', '0.3477', '-0.083', '-0.0662', '-0.1792', '-0.574', '0.932', '0.2642', '0.305', '0.0002828', '-0.6133', '0.3125', '-0.4744', '1.021', '0.593', '0.3186', '0.1409', '-0.2234', '0.3928', '-0.1876', '0.4524', '0.939', '-0.394', '0.517', '-0.787']",,,,,,,
mondo:0013395,retinitis pigmentosa 4,"['retinitis pigmentosa 4, autosomal dominant or recessive', 'retinitis pigmentosa caused by mutation in RHO', 'RP 4', 'retinitis pigmentosa, rhodopsin-related', 'RP4', 'retinitis pigmentosa type 4', 'retinitis pigmentosa 4', 'RHO retinitis pigmentosa']",0110372,613731,,C3151001,,,,C566706,,H35.5,,
mondo:0013396,chromosome 1p32-p31 deletion syndrome,"['Del(1)(p31p32)', 'BRMUTD', 'brain malformations with or without urinary tract defects', 'chromosome 1p32-p31 deletion syndrome', 'monosomy 1p31p32', '1p31p32 microdeletion syndrome']",0060409,,401986,CN226149,"['0.1428', '-0.0353', '0.6904', '-0.3892', '-0.06146', '-0.00357', '0.1267', '0.2676', '-0.6177', '-0.02751', '-0.535', '-0.2147', '-0.05692', '0.001436', '-0.04468', '0.02687', '0.06027', '-0.2206', '-0.05444', '-0.395', '0.05585', '0.002605', '0.2491', '-0.4783', '0.1494', '-0.3198', '-0.2812', '0.031', '0.4504', '-0.1467', '0.2274', '-0.03357', '0.3274', '0.1917', '-0.1403', '-0.07355', '-0.2869', '-0.0511', '-0.1893', '-0.4294', '-0.1324', '0.014', '0.2126', '-0.09296', '0.02931', '-0.4648', '0.3767', '0.395', '-0.2512', '0.04446', '-0.4268', '0.24', '-0.433', '-0.1716', '-0.4736', '-0.11694', '0.00382', '-0.3118', '-0.128', '0.53', '-0.3906', '-6.5e-06', '-0.10205', '0.3071', '-0.1592', '0.466', '0.2947', '0.169', '-0.7495', '0.396', '-0.7373', '0.6304', '-0.1493', '-0.09296', '-0.3333', '0.0883', '0.5166', '-0.06213', '-0.1223', '0.408', '0.03345', '0.2627', '0.3164', '0.7676', '0.0504', '0.0921', '0.676', '0.5737', '0.501', '-0.02539', '-0.4102', '0.8994', '0.2051', '-0.1566', '1.142', '-0.03546', '0.6763', '0.01976', '0.531', '0.4849']",,,,,,,
mondo:0013397,"acne inversa, familial, 2","['acne inversa, familial, type 2', 'acne inversa, familial, 2', 'ACNINV2', 'acne inversa, familial, 2, with or without Dowling-Degos disease', 'PSENEN familial acne inversa', 'familial acne inversa caused by mutation in PSENEN']",,613736,,C3151037,,,,,,,,
mondo:0013398,"acne inversa, familial, 3","['ACNINV3', 'acne inversa, familial, 3', 'familial acne inversa caused by mutation in PSEN1', 'acne inversa, familial, type 3', 'PSEN1 familial acne inversa']",,613737,,C3151038,,,,,,,,
mondo:0013400,"Congenital adrenal insuffiency with 46, XY sex reversal OR 46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency","['XY sex reversal-adrenal failure syndrome', 'adrenal insufficiency, congenital, with 46,XY SEX reversal, partial or complete', '46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency', 'XY sex reversal-adrenal failure', 'cholesterol side-chain cleavage deficiency', 'p450scc deficiency', '46,XY disorder of sex development-adrenal insufficiency due to CYP11A1 deficiency syndrome', 'adrenal insufficiency, congenital, with 46XY sex reversal, partial or complete']",0050546,613743,168558,C3151055,"['-1.105', '0.06146', '-0.1405', '-0.2001', '0.2722', '-0.1602', '-0.1588', '0.5864', '-0.4707', '-0.3584', '-0.1602', '-0.1583', '-0.0711', '0.4307', '0.2069', '-0.271', '0.6025', '0.3047', '-0.561', '-0.5044', '0.1246', '-0.3762', '0.5923', '-0.0681', '0.3843', '0.1064', '0.2878', '0.2386', '0.10046', '-0.641', '0.416', '0.2146', '0.745', '0.05093', '-0.3147', '-0.4226', '-0.02412', '0.03146', '-0.2554', '-0.2925', '0.2788', '0.0904', '0.06027', '0.01665', '-0.381', '-0.4556', '0.3135', '-0.05917', '0.10046', '0.484', '0.0689', '-0.2556', '-0.2224', '0.2094', '-0.3513', '0.3125', '0.5464', '-0.475', '-0.0759', '0.4333', '0.1727', '0.4321', '0.308', '0.11554', '0.03732', '0.478', '0.2365', '0.5864', '-0.3872', '-0.124', '-0.4739', '0.358', '0.285', '0.3118', '0.1438', '-0.2864', '0.2617', '0.1716', '-0.393', '-0.1373', '0.061', '0.5757', '0.4517', '-0.106', '-0.12036', '0.2393', '0.1954', '-0.05627', '0.5034', '-0.139', '0.07355', '0.5093', '-0.3838', '-0.2874', '0.2659', '-0.0161', '0.3337', '-0.4246', '-0.3628', '0.4583']",C131422,,C566130,,,,
mondo:0013401,hereditary spastic paraplegia 51,"['cerebral palsy, spastic quadriplegic, 4, formerly', 'CPSQ4', 'spastic quadriplegic cerebral palsy 4', 'AP4E1 hereditary spastic paraplegia', 'SPG51', 'hereditary spastic paraplegia type 51', 'autosomal dominant spastic paraplegia 51', 'hereditary spastic paraplegia caused by mutation in AP4E1', 'spastic paraplegia 51, autosomal recessive', 'cerebral palsy, spastic quadriplegic, 4']",0110803,613744,,C3151056,,,,,,,,
mondo:0013402,retinitis pigmentosa 27,"['retinitis pigmentosa caused by mutation in NRL', 'RP27', 'retinitis pigmentosa type 27', 'retinal Degeneration, autosomal recessive, Clumped pigment type', 'NRL retinitis pigmentosa', 'retinitis pigmentosa 27']",0110397,613750,,C1834329,,,,C563526,,H35.5,,
mondo:0013403,"heterotaxy, visceral, 4, autosomal","['heterotaxy, visceral, 4, autosomal', 'visceral heterotaxy caused by mutation in ACVR2B', 'HTX4', 'ACVR2B visceral heterotaxy']",,613751,,C3151057,,,,,,,,
mondo:0013404,hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase,"['psychomotor retardation due to S-adenosylhomocysteine hydrolase deficiency', 'hypermethioninemia with S-adenosylhomocysteine hydrolase deficiency', 'hypermethioninemia due to S-adenosylhomocysteine hydrolase deficiency']",0111039,613752,88618,C4510276,"['-0.5913', '0.2079', '-0.1646', '-0.08856', '0.8184', '-0.266', '-0.594', '0.995', '-0.826', '-0.2422', '-0.5005', '-0.565', '0.156', '0.01938', '0.0199', '0.3284', '-0.1171', '-0.2225', '-0.7124', '-1.13', '0.6274', '-0.625', '0.436', '0.03848', '0.1588', '-0.1904', '0.4578', '0.566', '0.00691', '-0.2576', '0.621', '-0.3062', '0.3984', '0.3882', '-0.86', '-0.3323', '-0.04727', '-0.2417', '0.525', '0.2096', '-0.0845', '-0.4805', '-0.1405', '0.2378', '-0.3481', '-0.1733', '0.198', '-0.2115', '-0.4216', '-0.0714', '0.3806', '0.0865', '0.07166', '-0.218', '-0.2615', '-0.4705', '-0.00829', '-0.4373', '-0.412', '0.8223', '-0.1378', '0.06152', '0.2358', '-0.3577', '-0.523', '-0.04102', '0.3657', '0.319', '-0.4114', '0.0733', '-0.1548', '0.4521', '-0.3435', '0.4548', '0.6973', '-0.0744', '0.2834', '-0.2455', '-0.0955', '0.198', '0.1736', '0.5874', '-0.1117', '0.2037', '-0.1234', '0.6807', '-0.276', '0.2441', '0.516', '-0.3313', '0.665', '0.7437', '-0.696', '-0.5044', '0.1298', '0.2642', '-0.0379', '-0.544', '-0.09143', '-0.5996']",,,,,,,
mondo:0013405,retinitis pigmentosa 49,"['RP49', 'retinitis pigmentosa type 49', 'retinitis pigmentosa caused by mutation in CNGA1', 'retinitis pigmentosa 49', 'CNGA1 retinitis pigmentosa']",0110377,613756,,C3151059,,,,,,H35.5,,
mondo:0013406,age related macular degeneration 6,"['RAX2 age-related macular degeneration', 'age-related macular degeneration caused by mutation in RAX2', 'ARMD6', 'macular degeneration, age-related, 6', 'age related macular degeneration type 6', 'macular Degeneration, age-related, type 6']",0110018,613757,,C3151060,,,,C563674,,,,
mondo:0013407,retinitis pigmentosa 47,"['retinitis pigmentosa caused by mutation in SAG', 'SAG retinitis pigmentosa', 'retinitis pigmentosa type 47', 'retinitis pigmentosa 47', 'RP47']",0110369,613758,,C3151061,,,,,,H35.5,,
mondo:0013408,FADD-related immunodeficiency,"['infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations', 'immunodeficiency 90 with encephalopathy, functional hyposplenia, and hepatic dysfunction', 'Fadd deficiency']",,613759,306550,C4509831,"['0.1692', '0.659', '-0.687', '-0.4197', '-0.1466', '-1.012', '0.4011', '-0.11273', '0.2288', '-0.2202', '0.05075', '-0.5054', '0.1796', '-0.3105', '0.1279', '0.463', '-0.0382', '0.1104', '-0.5093', '-0.581', '0.9854', '-0.3936', '0.343', '-0.6978', '0.1482', '0.1357', '-0.4282', '0.2145', '0.624', '-0.689', '0.6807', '-0.08057', '0.244', '-0.1654', '0.02882', '-0.099', '-0.6533', '-0.3235', '-0.4006', '-0.1895', '-0.3352', '-0.4263', '0.508', '-0.1199', '0.02078', '0.12445', '0.05682', '-0.4995', '-0.392', '0.5083', '-0.2874', '-0.05188', '0.1659', '0.0626', '0.0739', '-0.1482', '0.5034', '-0.268', '-0.01602', '0.5376', '0.1266', '-0.06198', '0.592', '0.3008', '-0.007286', '0.10065', '0.4092', '0.2001', '-0.402', '1.038', '-0.514', '0.2466', '-0.2045', '0.4766', '0.09216', '0.0003805', '0.675', '0.1436', '-0.01124', '-0.3162', '-0.2974', '0.2197', '0.24', '-0.2751', '0.00229', '0.4487', '0.5537', '0.792', '0.14', '0.3389', '0.166', '0.4365', '0.0885', '0.2852', '1.215', '1.038', '0.2158', '-0.2505', '-0.3005', '-0.8306']",,,,,,,
mondo:0013409,age related macular degeneration 5,"['macular degeneration, age-related, 5', 'age-related macular degeneration caused by mutation in ERCC6', 'macular Degeneration, age-related, type 5', 'ARMD5', 'macular degeneration, age-related, susceptibility to, 5', 'ERCC6 age-related macular degeneration', 'age related macular degeneration type 5']",0110028,613761,,C3151063,,,,,,,,
mondo:0013410,"46,XY sex reversal 6","['SRXY6', '46,XY Sex reversal type 6', '46,XY gonadal dysgenesis, partial or complete, Map3K1-related', '46,XY sex reversal 6', '46,XY Sex reversal, partial or complete, Map3K1-related', '46,XY SEX reversal 6', '46XY sex reversal 6']",0111769,613762,,C3151064,,,,,,,,
mondo:0013411,cataract 16 multiple types,"['cataract, posterior polar, 2', 'CRYAB early-onset non-syndromic cataract', 'CTRCT16', 'cataract 16, multiple types', 'early-onset non-syndromic cataract caused by mutation in CRYAB', 'posterior polar cataract 2', 'cataract, congenital lamellar', 'CTPP2']",0110250,613763,,,"['-0.001651', '0.02225', '-0.007267', '-0.005363', '0.01675', '-0.02246', '-0.004333', '0.0376', '-0.02782', '-0.004417', '0.0001985', '0.007786', '-0.008255', '0.01052', '-0.011246', '-0.02327', '-0.005684', '-0.01499', '-0.01139', '-0.04086', '0.002935', '-0.006657', '0.02344', '-0.005947', '0.013916', '-0.002367', '-0.00757', '0.008095', '0.002563', '-0.014725', '0.03537', '-0.006733', '0.02644', '0.000195', '0.01875', '-0.01567', '-0.003487', '-0.005985', '0.002663', '-0.014885', '0.0199', '-0.0369', '0.010735', '-0.01294', '0.004467', '-0.03424', '-0.00854', '0.03108', '0.01127', '-0.00728', '-0.00999', '-0.00908', '0.0004888', '0.00815', '-0.00841', '-0.01022', '0.03111', '-0.01082', '-0.031', '0.00782', '0.02063', '-0.001357', '0.00878', '0.01274', '0.001564', '0.002571', '0.03111', '0.02335', '-0.02435', '0.0183', '-0.014854', '0.004627', '0.001674', '-0.0314', '0.02109', '0.0239', '0.001463', '-0.00943', '-0.02258', '-0.01628', '-0.010605', '0.006428', '-0.001558', '0.03123', '-0.010086', '-0.001435', '0.02158', '0.01755', '0.03503', '0.01651', '0.01281', '0.03738', '-0.003862', '0.000824', '0.05292', '0.02585', '0.02768', '-0.0331', '0.001585', '0.006477']",,,C565134,,,,
mondo:0013412,hypertrophic cardiomyopathy 9,"['CMH9', 'cardiomyopathy, familial hypertrophic, 9', 'hypertrophic cardiomyopathy type 9', 'cardiomyopathy, familial hypertrophic, type 9', 'TTN hypertrophic cardiomyopathy', 'hypertrophic cardiomyopathy caused by mutation in TTN']",0110315,613765,,C1861065,,,,C566044,,,,
mondo:0013413,retinitis pigmentosa 45,"['CNGB1 retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in CNGB1', 'retinitis pigmentosa 45', 'retinitis pigmentosa type 45', 'RP45']",0110402,613767,,C3151066,,,,,,H35.5,,
mondo:0013414,retinitis pigmentosa 44,"['retinitis pigmentosa type 44', 'retinitis pigmentosa caused by mutation in RGR', 'RGR retinitis pigmentosa', 'RP44', 'retinitis pigmentosa 44']",0110394,613769,,C3151068,,,,,,H35.5,,
mondo:0013415,chromosome 17p13.1 deletion syndrome,"['chromosome 17p13.1 deletion syndrome', '17p13.1 deletion syndrome']",0060402,613776,,C3151069,,,,,,,,
mondo:0013416,age related macular degeneration 8,"['age related macular degeneration type 8', 'age-related macular degeneration caused by mutation in ARMS2', 'ARMD8', 'macular Degeneration, age-related, type 8', 'macular degeneration, age-related, 8', 'ARMS2 age-related macular degeneration']",0110020,613778,,C3151070,,,,,,,,
mondo:0013417,complement component 3 deficiency,"['classic complement early component deficiency caused by mutation in C3', 'C3d', 'complement component 3 deficiency, autosomal recessive', 'C3 deficiency', 'C3 deficiency, autosomal recessive', 'C3 classic complement early component deficiency']",8354,613779,280133,C3151071,"['-0.1323', '0.493', '-0.323', '0.1697', '-0.3435', '-0.2502', '0.355', '-0.3838', '0.04514', '-0.1207', '-0.07794', '0.1163', '0.1038', '0.04465', '0.1802', '-0.1774', '-0.1465', '0.1691', '-0.2737', '-0.833', '-0.0505', '-0.5146', '0.901', '-0.565', '0.4968', '0.3374', '-0.1033', '0.4946', '-0.1924', '-0.057', '0.4146', '0.551', '0.4268', '0.2573', '-0.1903', '-0.1366', '-0.1829', '0.07825', '-0.436', '-0.2495', '-0.3264', '0.0862', '0.06934', '-0.287', '-0.0735', '-0.612', '0.04016', '-0.4558', '0.374', '0.7666', '-0.2954', '0.1577', '0.3452', '-0.3247', '-0.648', '0.1797', '0.0715', '-0.2103', '-0.1525', '0.2144', '0.3271', '0.4426', '0.1299', '0.3098', '0.2966', '0.0771', '0.8135', '0.4065', '-0.162', '0.3142', '-0.928', '-0.3945', '-0.1578', '0.03564', '0.2184', '-0.00896', '0.2815', '0.292', '0.3494', '-0.03064', '-0.1827', '-0.4004', '0.8022', '0.2793', '-0.05075', '-0.3625', '0.2742', '-0.01133', '-0.004242', '0.1792', '0.506', '0.3904', '-0.3386', '-0.2072', '0.371', '1.071', '-0.01845', '-0.46', '-0.2622', '-0.1107']",C9468,,C565169,,,,
mondo:0013418,"aortic aneurysm, familial thoracic 7","['aortic dissection, familial, with or without aortic aneurysm', 'aortic aneurysm, familial thoracic 7', 'AAT7', 'aortic aneurysm, familial thoracic type 7']",,613780,,C3151077,,,,,,,,
mondo:0013419,complement component C1s deficiency,"['C1SD', 'complement component C1s deficiency', 'C1s deficiency']",,613783,,C3151078,"['-0.0456', '0.06055', '-0.00881', '0.00988', '0.01593', '-0.0352', '0.01115', '0.01924', '-0.03014', '-0.03983', '-0.01804', '-0.002125', '0.0008893', '0.0113', '-0.01411', '-0.05542', '-0.006516', '-0.0116', '-0.05734', '-0.1053', '0.014046', '-0.05536', '0.0759', '-0.007126', '0.01491', '-0.02425', '0.002617', '-0.01231', '-0.003103', '-0.03397', '0.05774', '0.01895', '0.0723', '0.03445', '0.01631', '-0.02953', '-0.008965', '-0.01642', '-0.02332', '-0.0875', '0.03326', '-0.0672', '0.01508', '-0.03806', '-0.004616', '-0.07697', '0.02814', '0.01881', '0.0359', '0.05005', '-0.0246', '-0.03387', '0.01909', '0.01788', '-0.05145', '-0.01956', '0.0609', '-0.04587', '-0.0753', '0.03004', '0.04947', '0.0167', '0.02739', '0.0105', '0.02274', '0.02457', '0.0845', '0.03406', '-0.05463', '0.08997', '-0.0486', '5.19e-05', '-0.00807', '-0.0561', '0.01924', '0.04465', '0.0378', '-0.00215', '-0.0238', '-0.01979', '-0.01367', '-0.01225', '-0.02173', '0.03888', '-0.02174', '-0.01906', '0.03833', '0.0397', '0.0865', '0.003178', '0.02644', '0.04584', '-0.00876', '0.00812', '0.12213', '0.0733', '0.05264', '-0.11194', '-0.02827', '0.04587']",,,C565170,,,,
mondo:0013420,age related macular degeneration 12,"['macular Degeneration, age-related, type 12', 'age-related macular degeneration caused by mutation in CX3CR1', 'CX3CR1 age-related macular degeneration', 'ARMD12', 'macular degeneration, age-related, 12', 'age related macular degeneration type 12']",0110024,613784,,C3151079,,,,,,,,
mondo:0013421,type II complement component 8 deficiency,"['C8 deficiency, type II', 'complement component 8 deficiency type II', 'Human complement C8-beta deficiency', 'C8 deficiency, type 2', 'C8 Beta deficiency', 'complement component 8 deficiency type 2', 'complement component 8 deficiency, type 2', 'complement component 8B deficiency', 'C8B classic complement early component deficiency', 'C8 deficiency type II', 'complement component 8 deficiency, type II', 'C8D2', 'C8B deficiency', 'classic complement early component deficiency caused by mutation in C8B']",0060302,613789,,C3151080,,,,,,,,
mondo:0013422,type I complement component 8 deficiency,"['C8Ag deficiency', 'C8 Alpha-gamma deficiency', 'C8 deficiency, type I', 'complement component 8 deficiency type I', 'C8 deficiency, type 1', 'C8D1', 'C81 deficiency', 'C8 deficiency type I', 'classic complement early component deficiency caused by mutation in C8A', 'complement component 8 deficiency type 1', 'complement component 8 deficiency, type 1', 'complement component 8 deficiency, type I', 'C8A classic complement early component deficiency']",0060301,613790,,C3151081,,,,,,,,
mondo:0013423,immunodeficiency due to MASP-2 deficiency,"['MASP2 deficiency', 'lectin complement activation pathway, defect in, 2']",,613791,331187,C3151085,"['-0.1466', '-0.161', '-0.1838', '-0.1141', '0.1694', '-0.003408', '0.2517', '-0.4802', '-0.19', '0.0043', '0.1194', '0.1519', '-0.2262', '0.0791', '0.0948', '0.0521', '-0.2935', '0.214', '-0.4314', '-0.6226', '0.176', '-0.2615', '0.729', '-0.02136', '-0.1043', '0.04465', '-0.2664', '0.11127', '-0.04797', '-0.3135', '0.3018', '0.2524', '0.694', '-0.0634', '0.1915', '-0.3132', '-0.3623', '0.12164', '0.01171', '-0.4302', '-0.1104', '0.1714', '0.2556', '-0.3545', '-0.2527', '-0.5825', '0.297', '0.002806', '-0.0424', '0.2474', '-0.3213', '0.035', '0.4788', '0.006325', '-0.455', '0.2808', '0.2844', '-0.2837', '-0.3972', '-0.1644', '0.1394', '0.3052', '0.00874', '-0.04175', '0.586', '0.002197', '0.4102', '0.3892', '-0.4006', '0.1826', '-0.4182', '-0.2673', '-0.267', '0.2373', '-0.1013', '0.02081', '0.6274', '0.2092', '0.0633', '-0.1849', '-0.2338', '-0.01157', '0.1209', '0.2465', '-0.1552', '-0.2852', '0.4778', '0.4294', '0.2424', '-0.1067', '0.5', '-0.02005', '-0.11707', '-0.431', '0.756', '0.8477', '0.2263', '-0.3213', '-0.0829', '0.1042']",,,C565360,,,,
mondo:0013424,3p- syndrome,"['chromosome 3, monosomy 3p25', 'distal monosomy type 3p', '3p- syndrome', '3p deletion', 'distal 3p deletion', 'chromosome 3pter-p25 deletion syndrome', 'distal monosomy 3p', 'deletion 3p25', 'chromosome 3p- syndrome', 'telomeric monosomy 3p', 'deletion 3p', 'del(3p25)', 'chromosome 3p deletion', 'monosomy 3p', '3p monosomy', 'partial monosomy 3p', 'monosomy 3pter', 'Del(3p) syndrome']",0060417,613792,1620,,,C41377,,C536804,,,,
mondo:0013425,retinitis pigmentosa 20,"['retinitis pigmentosa 20', 'retinitis pigmentosa type 20', 'RPE65 retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in RPE65', 'RP20', 'RP 20']",0110353,613794,,C3151086,,,,C566718,,H35.5,,
mondo:0013426,aneurysm-osteoarthritis syndrome,"['Loeys-Dietz syndrome type 3', 'Loeys-Dietz syndrome, type 1C, formerly', 'Loeys-Dietz syndrome 3', 'LDS3', 'Loeys-Dietz syndrome, type 1C', 'Loeys-Dietz syndrome with osteoarthritis', 'aneurysm - osteoarthritis syndrome', 'aneurysms-osteoarthritis syndrome', 'Loeys-Dietz syndrome, type 3', 'Loeys-Dietz syndrome, type 1C (formerly)']",0070237,613795,284984,C3151087,"['-0.1012', '0.0668', '0.4922', '0.07513', '0.3274', '-0.4812', '0.0354', '0.2805', '-0.31', '-0.541', '0.012596', '0.3943', '0.427', '0.588', '-0.264', '-0.0537', '-0.05145', '0.01048', '-0.4128', '-0.597', '0.6655', '0.4158', '-0.02559', '-0.0359', '-0.556', '0.1803', '0.49', '-0.4873', '0.8667', '0.05585', '0.05173', '-0.1422', '0.824', '0.4214', '0.9995', '-0.4038', '-0.0952', '-0.4993', '0.2457', '-0.8384', '1.02', '0.483', '-0.6733', '0.2778', '0.1036', '0.1616', '0.2612', '0.665', '0.06052', '-0.319', '-0.07275', '0.3784', '0.5703', '0.1993', '0.3467', '-0.4895', '-0.162', '0.007256', '-0.3718', '-0.1382', '0.8496', '0.2576', '-0.874', '-0.6074', '-0.532', '-0.1404', '0.2441', '1.01', '0.278', '0.7036', '-0.03622', '0.3828', '0.01807', '-0.2084', '-0.0845', '0.0776', '0.277', '0.9697', '0.0715', '-0.625', '-0.64', '-0.0641', '0.3264', '0.3975', '0.4778', '0.29', '-0.323', '0.5156', '0.1267', '0.06256', '0.05457', '0.6016', '0.10876', '0.09045', '0.0348', '-0.01674', '0.489', '-0.3323', '-0.3347', '-0.0992']",,,,,,,
mondo:0013427,immunodeficiency 31B,"['Stat1 deficiency, autosomal recessive', 'immunodeficiency 31B, mycobacterial and viral infections, autosomal recessive', 'STAT1 deficiency', 'susceptibility to viral and mycobacterial infections', 'IMD31B', 'immunodeficiency type 31B', 'immunodeficiency 31B']",0111944,613796,391311,C3151088,"['-0.12305', '0.188', '0.302', '-0.2737', '0.0929', '-0.3225', '0.2527', '-0.2263', '0.0398', '0.1436', '0.00509', '0.09406', '-0.0418', '0.02419', '-0.1754', '-0.1522', '0.0422', '0.1926', '-0.0996', '-0.5176', '-0.1052', '-0.111', '0.586', '-0.0853', '-0.2798', '0.05344', '-0.2566', '0.1128', '-0.0914', '-0.4858', '0.0009484', '0.3096', '0.4106', '0.0248', '0.204', '-0.2223', '-0.156', '-0.01144', '-0.2773', '-0.3918', '-0.168', '-0.08026', '0.2043', '-0.01894', '-0.3218', '-0.4163', '-0.05978', '-0.0354', '0.1389', '0.2947', '-0.0948', '-0.1471', '0.2666', '-0.2158', '-0.1432', '-0.00998', '0.2074', '-0.33', '-0.229', '0.2228', '-0.133', '0.2966', '0.1327', '0.2126', '0.3672', '0.01608', '0.3848', '0.11115', '-0.257', '0.3079', '-0.2478', '-0.1368', '0.03854', '-0.1299', '0.1638', '0.0524', '0.09485', '0.1631', '0.05215', '0.17', '-0.3013', '0.08826', '-0.02318', '0.2515', '-0.0744', '0.03467', '0.286', '0.1964', '0.452', '-0.08545', '0.2468', '0.3745', '-0.0944', '-0.1694', '0.51', '0.591', '0.482', '-0.4863', '-0.0923', '-0.0702']",,,,,,,
mondo:0013428,Meier-Gorlin syndrome 2,"['Meier-GORLIN syndrome 2', 'Meier-Gorlin syndrome type 2', 'ORC4 Meier-Gorlin syndrome', 'Meier-Gorlin syndrome 2', 'MGORS2', 'Meier-Gorlin syndrome caused by mutation in ORC4']",0080513,613800,,C3151097,,,,,,,,
mondo:0013429,retinitis pigmentosa 40,"['PDE6B retinitis pigmentosa', 'RP40', 'retinitis pigmentosa caused by mutation in PDE6B', 'retinitis pigmentosa type 40', 'retinitis pigmentosa 40', 'retinitis pigmentosa-40']",0110375,613801,,C3151107,,,,,,H35.5,,
mondo:0013430,Meier-Gorlin syndrome 3,"['Meier-Gorlin syndrome 3', 'Meier-GORLIN syndrome 3', 'Meier-Gorlin syndrome type 3', 'MGORS3', 'Meier-Gorlin syndrome caused by mutation in ORC6', 'ORC6 Meier-Gorlin syndrome']",0080514,613803,,C3151113,,,,,,,,
mondo:0013431,Meier-Gorlin syndrome 4,"['CDT1 Meier-Gorlin syndrome', 'MGORS4', 'Meier-GORLIN syndrome 4', 'Meier-Gorlin syndrome caused by mutation in CDT1', 'Meier-Gorlin syndrome 4', 'Meier-Gorlin syndrome type 4']",0080515,613804,,C3151120,,,,,,,,
mondo:0013432,Meier-Gorlin syndrome 5,"['Meier-Gorlin syndrome type 5', 'Meier-Gorlin syndrome caused by mutation in CDC6', 'MGORS5', 'Meier-GORLIN syndrome 5', 'CDC6 Meier-Gorlin syndrome', 'Meier-Gorlin syndrome 5']",0080516,613805,,C3151126,,,,,,,,
mondo:0013433,primary sclerosing cholangitis,"['PSC', 'cholangitis, primary sclerosing']",0060643,613806,171,C0566602,,,,,,,10036732,
mondo:0013434,primary ciliary dyskinesia 14,"['ciliary dyskinesia, primary, 14', 'ciliary dyskinesia, primary, 14, with or without situs inversus', 'primary ciliary dyskinesia 14 with or without situs inversus', 'primary ciliary dyskinesia caused by mutation in CCDC39', 'primary ciliary dyskinesia type 14', 'CCDC39 primary ciliary dyskinesia', 'CILD14', 'ciliary dyskinesia, primary, type 14']",0110598,613807,,C3151136,,C148370,,,,,,
mondo:0013435,primary ciliary dyskinesia 15,"['ciliary dyskinesia, primary, 15', 'CCDC40 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, type 15', 'primary ciliary dyskinesia caused by mutation in CCDC40', 'primary ciliary dyskinesia type 15', 'CILD15', 'primary ciliary dyskinesia 15 with or without situs inversus', 'ciliary dyskinesia, primary, 15, with or without situs inversus']",0110623,613808,,C3151137,,C155999,,,,,,
mondo:0013436,retinitis pigmentosa 39,"['retinitis pigmentosa caused by mutation in USH2A', 'USH2A retinitis pigmentosa', 'RP39', 'retinitis pigmentosa 39', 'retinitis pigmentosa type 39']",0110360,613809,,C3151138,,,,,,H35.5,,
mondo:0013437,retinitis pigmentosa 43,"['PDE6A retinitis pigmentosa', 'retinitis pigmentosa type 43', 'retinitis pigmentosa 43', 'RP43', 'retinitis pigmentosa caused by mutation in PDE6A']",0110379,613810,,C3151139,,,,,,H35.5,,
mondo:0013438,pontocerebellar hypoplasia type 2D,"['pontocerebellar hypoplasia, type 2D', 'SEPSECS non-syndromic pontocerebellar hypoplasia', 'Cerebellocerebral atrophy, progressive', 'PCH2D', 'non-syndromic pontocerebellar hypoplasia caused by mutation in SEPSECS', 'cerebello-cerebral atrophy, progressive']",0060270,613811,,C3151140,,,,,,,,
mondo:0013439,congenital bile acid synthesis defect 3,"['bile acid synthesis defect, congenital, 3', 'BASD3', 'bile acid synthesis defect, congenital, type 3', 'CBAS3', 'oxysterol 7-alpha-hydroxylase deficiency', 'congenital bile acid synthesis defect type 3', 'CYP7B1 congenital bile acid synthesis defect', 'congenital bile acid synthesis defect caused by mutation in CYP7B1']",0111070,613812,79302,C4304715,"['-0.1426', '0.1571', '0.0828', '-0.0804', '0.4756', '-0.5693', '-0.6943', '0.7764', '0.0443', '-0.1647', '-0.501', '-0.4812', '-0.07715', '0.1821', '-0.542', '-0.535', '-0.1865', '-0.3782', '0.1472', '-0.9463', '0.2717', '-0.6895', '0.666', '-0.3706', '0.305', '0.0779', '-0.2457', '0.394', '-0.1378', '-0.5435', '0.3875', '0.4785', '0.2761', '0.3167', '-0.4458', '-0.688', '-0.5747', '-0.1378', '0.297', '0.1583', '0.048', '-0.7603', '0.2031', '0.02892', '-0.7417', '-0.06714', '0.5366', '-0.05814', '-0.0965', '-0.531', '0.0348', '0.0005016', '0.1234', '-0.3154', '-0.582', '-0.4612', '0.1361', '0.00601', '-0.505', '0.395', '0.4216', '-0.16', '0.68', '-0.5366', '0.3284', '0.1572', '0.85', '0.1857', '-0.553', '-0.3413', '-0.4983', '0.341', '-0.1455', '0.656', '0.489', '0.014404', '-0.02283', '-0.1097', '-0.2161', '0.556', '-0.6064', '0.7207', '-0.7305', '-0.2076', '-0.378', '0.1131', '0.4539', '0.09796', '0.09845', '-0.201', '0.4153', '0.559', '-0.014275', '-0.3022', '0.8145', '0.1266', '0.394', '-0.68', '0.03093', '-0.2072']",,,C566340,,,,
mondo:0013440,autosomal recessive limb-girdle muscular dystrophy type 2P,"['muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 9', 'muscular dystrophy-dystroglycanopathy (limb-girdle) type C9', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in DAG1', 'muscular dystrophy, limb-girdle, type 2P', 'muscular dystrophy-dystroglycanopathy limb-girdle DAG1-related', 'muscular dystrophy-dystroglycanopathy, limb-girdle, Dag1-related', 'MDDGC9', 'DAG1 autosomal recessive limb-girdle muscular dystrophy', 'limb-girdle muscular dystrophy type 2P', 'LGMD2P']",0110293,613818,280333,C3151184,"['-0.021', '-0.5845', '-0.3538', '-0.228', '0.281', '-1.102', '-0.02011', '0.617', '-1.554', '-0.91', '-0.1339', '0.417', '-0.1442', '1.012', '0.3132', '0.1635', '-0.78', '-0.3696', '-0.266', '-0.647', '-0.0998', '0.2822', '0.178', '0.393', '0.0619', '-0.3315', '-0.2637', '-0.773', '0.07635', '-0.206', '0.813', '-0.2725', '0.779', '0.1477', '0.166', '0.133', '-0.686', '-0.02046', '0.2467', '-0.4202', '-0.03485', '-0.469', '-0.6313', '0.3833', '-0.03723', '0.2925', '-0.11725', '0.737', '-0.1569', '0.3376', '0.1722', '-0.4382', '0.361', '-0.797', '0.07294', '-0.3774', '0.2668', '0.9893', '-0.3186', '0.01444', '0.05386', '-0.1779', '-0.096', '-0.10614', '0.01536', '0.2869', '-0.0763', '0.463', '-0.4478', '-0.0864', '-0.2295', '0.1122', '0.186', '-0.0802', '0.844', '0.54', '-0.2834', '0.0464', '-0.2137', '-0.0505', '0.09344', '-0.2155', '-0.0207', '0.3396', '-0.1007', '0.2566', '-0.1206', '-0.3386', '0.9126', '0.3547', '-0.3623', '0.1074', '0.1844', '0.842', '-0.10834', '0.3418', '0.3557', '-0.574', '0.2424', '-0.361']",,,,,,,
mondo:0013441,asphyxiating thoracic dystrophy 4,"['short-rib thoracic dysplasia 4 with or without polydactyly', 'asphyxiating thoracic dystrophy type 4', 'SRTD4', 'ATD4', 'asphyxiating thoracic dystrophy 4']",0110088,613819,,C3151185,,,,,,,,
mondo:0013442,nephronophthisis 12,"['NPHP12', 'nephronophthisis type 12', 'TTC21B nephronophthisis (disease)', 'Joubert syndrome 11', 'nephronophthisis 12']",0111119,613820,,C3151186,,,,,,,,
mondo:0013443,Seckel syndrome 5,"['SCKL5', 'Seckel syndrome caused by mutation in CEP152', 'Seckel syndrome 5', 'CEP152 Seckel syndrome', 'Seckel syndrome type 5']",0070012,613823,,C3151187,,,,,,,,
mondo:0013444,nephronophthisis 9,"['nephronophthisis type 9', 'nephronophthisis 9', 'NPHP9', 'NEK8 nephronophthisis (disease)']",0111120,613824,,C3151188,,,,,,,,
mondo:0013445,complement component 9 deficiency,"['complement component 9 deficiency', 'C9 deficiency', 'classic complement early component deficiency caused by mutation in C9', 'C9D', 'C9 classic complement early component deficiency']",0060303,613825,,C3151189,,,,C565165,,,,
mondo:0013446,Leber congenital amaurosis 6,"['Leber congenital amaurosis 6', 'RPGRIP1 Leber congenital amaurosis', 'Leber congenital amaurosis type 6', 'Leber congenital amaurosis caused by mutation in RPGRIP1', 'LCA6']",0110329,613826,,,,,,C565327,,H35.5,,
mondo:0013447,retinitis pigmentosa 48,"['retinitis pigmentosa type 48', 'GUCA1B retinitis pigmentosa', 'retinitis pigmentosa 48', 'retinitis pigmentosa caused by mutation in GUCA1B', 'RP48']",0110382,613827,,C3151190,,,,,,H35.5,,
mondo:0013448,"generalized epilepsy with febrile seizures plus, type 8","['GEFSP8', 'generalized epilepsy with febrile seizures plus, type 8', 'Gefs+, type 8']",0111299,613828,,C3151191,,,,,,,,
mondo:0013449,Leber congenital amaurosis 7,"['CRX Leber congenital amaurosis', 'Leber congenital amaurosis type 7', 'Leber congenital amaurosis caused by mutation in CRX', 'Leber congenital amaurosis 7', 'LCA7']",0110333,613829,,C3151192,,,,,,H35.5,,
mondo:0013450,congenital stationary night blindness 1D,"['night blindness, congenital stationary, type 1D', 'Csnb, complete, autosomal recessive', 'night blindness, congenital stationary (complete), 1D, autosomal recessive', 'congenital stationary night blindness caused by mutation in SLC24A1', 'congenital stationary night blindness 1D autosomal recessive', 'congenital stationary night blindness type 1D', 'CSNB1D', 'SLC24A1 congenital stationary night blindness']",0110868,613830,,C3151193,,,,,,,,
mondo:0013452,multisystemic smooth muscle dysfunction syndrome,"['multisystemic smooth muscle dysfunction syndrome', 'congenital mydriasis, patent ductus arteriosus, thoracic aortic aneurysm, and vasculopathy', 'mydriasis, congenital, with patent ductus arteriosus, thoracic aortic aneurysm, and vasculopathy']",,613834,404463,C3151201,"['-1.097', '0.1317', '0.31', '-0.249', '0.07715', '-0.4858', '-0.02321', '0.042', '-0.3486', '-0.04196', '0.0748', '-0.1455', '0.1736', '-0.556', '-0.287', '0.1329', '-0.219', '0.4253', '-0.561', '-0.8267', '0.4656', '0.5137', '-0.2644', '-0.1515', '-0.1962', '0.06464', '0.3', '-0.09265', '0.4414', '0.3403', '1.016', '0.2086', '0.5254', '-0.02179', '0.7695', '-0.1875', '-0.012054', '0.6597', '0.397', '-0.57', '-0.1613', '0.0781', '0.1103', '0.00652', '-0.0826', '0.0202', '0.2076', '-0.03317', '0.3677', '0.436', '-0.2588', '0.6357', '0.5073', '-0.3762', '-0.3936', '-0.11755', '0.4058', '-0.06256', '0.2214', '-0.2233', '0.5337', '0.4316', '0.1887', '-0.574', '-0.166', '0.4233', '0.3762', '0.4255', '-0.469', '0.837', '-0.4187', '0.1561', '0.1416', '0.3447', '-0.3484', '-0.3445', '0.229', '0.0665', '-0.07336', '0.0817', '0.1765', '-0.119', '0.583', '0.4277', '-0.2324', '-0.04602', '0.328', '0.2008', '0.508', '-0.4387', '0.2632', '-0.1813', '0.258', '0.04785', '0.7217', '0.11865', '0.3604', '-0.3552', '-0.185', '0.4404']",,,,,,,
mondo:0013453,Leber congenital amaurosis 8,"['Leber congenital amaurosis caused by mutation in CRB1', 'Leber congenital amaurosis type 8', 'CRB1 Leber congenital amaurosis', 'Leber congenital amaurosis 8', 'LCA8']",0110079,613835,,C3151202,,,,,,H35.5,,
mondo:0013454,Leber congenital amaurosis 11,"['IMPDH1 Leber congenital amaurosis', 'Leber congenital amaurosis 11', 'Leber congenital amaurosis type 11', 'LCA11', 'Leber congenital amaurosis caused by mutation in IMPDH1', 'amaurosis congenita of Leber, type 11']",0110216,613837,,C1840284,,,,C564140,,H35.5,,
mondo:0013455,hypertrophic cardiomyopathy 16,"['CMH16', 'hypertrophic cardiomyopathy type 16', 'cardiomyopathy, familial hypertrophic, 16', 'cardiomyopathy, hypertrophic, 16', 'hypertrophic cardiomyopathy caused by mutation in MYOZ2', 'MYOZ2 hypertrophic cardiomyopathy', 'cardiomyopathy, familial hypertrophic, type 16', 'cardiomyopathy familial hypertrophic 16']",0110322,613838,,C3151204,,,,,,,,
mondo:0013456,constitutional megaloblastic anemia with severe neurologic disease,"['megaloblastic anemia due to dihydrofolate reductase deficiency', 'DHFR deficiency', 'dihydrofolate reductase deficiency', 'megaloblastic anaemia due to dihydrofolate reductase deficiency']",,613839,319651,,"['-0.2294', '0.3599', '-0.2288', '0.4744', '0.643', '-0.08936', '-0.2866', '0.49', '-0.1661', '-0.2957', '0.8535', '-0.0616', '0.1786', '0.5527', '-1.171', '0.002237', '-0.671', '0.2585', '-0.561', '-0.3904', '-0.2323', '-0.539', '0.3489', '-0.418', '0.6216', '-0.6187', '0.03333', '-0.3625', '0.6035', '0.3213', '0.182', '0.10834', '0.449', '0.6562', '0.4956', '-0.1685', '-0.993', '-0.4187', '0.5186', '-0.592', '-0.5664', '0.33', '0.1482', '-0.377', '-0.884', '-0.9536', '0.3489', '0.2313', '0.5396', '-0.2124', '0.4602', '0.5083', '0.798', '-0.2262', '0.4143', '-0.8604', '0.1255', '0.564', '-1.152', '0.2145', '-0.1251', '0.3906', '-0.1807', '-0.2764', '-0.2428', '0.2107', '0.09296', '0.798', '-0.762', '1.039', '0.949', '-0.1902', '-0.4712', '-0.8545', '0.259', '1.131', '0.2837', '0.2864', '-0.005707', '0.5', '0.2194', '-0.2612', '-0.0421', '0.1509', '0.532', '-0.477', '-0.701', '0.4749', '0.9517', '-0.0745', '0.589', '0.2015', '-0.2085', '0.1917', '0.3623', '0.993', '0.07916', '-0.1342', '0.1982', '-0.355']",,,C565095,,,,
mondo:0013457,Leber congenital amaurosis 15,"['Leber congenital amaurosis 15', 'LCA15', 'Leber congenital amaurosis type 15', 'Leber congenital amaurosis caused by mutation in TULP1', 'TULP1 Leber congenital amaurosis', 'retinitis pigmentosa, juvenile, Tulp1-related']",0110189,613843,,C3151206,,,,,,H35.5,,
mondo:0013458,hyperuricemia-pulmonary hypertension-renal failure-alkalosis syndrome,"['HUPRA syndrome', 'hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome', 'hyperuricemia, pulmonary hypertension, renal failure, and alkalosis', 'HUPRAS', 'Hupra syndrome']",,613845,363694,C3151209,"['-0.1027', '-0.293', '0.01987', '0.2988', '0.4658', '-0.5366', '0.5684', '0.543', '-0.3738', '0.3892', '0.104', '-0.1569', '0.0465', '0.344', '-0.5625', '-0.312', '-0.7188', '0.2651', '0.0684', '-0.3513', '0.2979', '0.2615', '0.04343', '-0.443', '0.10547', '-0.2079', '0.5337', '0.4814', '-0.1996', '0.04877', '0.8325', '0.1543', '0.9707', '0.3523', '-0.1843', '-0.1006', '-0.722', '0.4395', '0.652', '-0.6655', '0.0909', '0.2084', '-0.3745', '0.393', '-0.05328', '0.1296', '0.0752', '0.1788', '0.351', '-0.4468', '-0.3833', '0.305', '-0.02515', '-0.4001', '0.4172', '-0.4155', '-0.3586', '0.2808', '-0.7183', '-0.0822', '0.1761', '1.014', '0.0606', '-0.447', '-0.0691', '-0.4019', '-0.07007', '0.5347', '-0.8774', '0.581', '-0.1119', '0.331', '0.511', '-0.04184', '-0.2009', '0.5723', '0.1946', '0.2069', '0.2335', '0.2747', '-0.1575', '-0.1004', '0.431', '-0.114', '0.5737', '-0.03012', '0.1572', '0.33', '0.4243', '0.1492', '0.502', '-0.6235', '-0.3296', '-0.1025', '0.853', '0.237', '0.4165', '-0.2169', '-0.522', '0.1981']",,,,,,,
mondo:0013459,osteogenesis imperfecta type 10,"['osteogenesis imperfecta type X', 'OI10', 'osteogenesis imperfecta, type X', 'osteogenesis imperfecta caused by mutation in SERPINH1', 'SERPINH1 osteogenesis imperfecta', 'osteogenesis imperfecta, type 10', 'OI, type 10', 'OI type 10', 'OI type X']",0110346,613848,216812,C3151211,,,,,,,,
mondo:0013460,osteogenesis imperfecta type 12,"['OI12', 'SP7 osteogenesis imperfecta', 'osteogenesis imperfecta type XII', 'osteogenesis imperfecta, type XII', 'osteogenesis imperfecta caused by mutation in SP7', 'OI, type 12', 'osteogenesis imperfecta, type 12']",0110348,613849,216820,C3151433,,,,,,,,
mondo:0013461,inosine triphosphatase deficiency,"['inosine triphosphatase deficiency', 'inosine triphosphate pyrophosphohydrolase deficiency']",,613850,319684,C0342800,"['-0.01063', '0.01756', '0.01239', '-0.005093', '0.01906', '-0.0251', '-0.006', '0.03064', '-0.01277', '-0.02037', '0.001655', '-0.003712', '-0.001498', '-9.793e-05', '-8.62e-05', '0.0002575', '-0.004707', '0.003845', '-0.02647', '-0.0437', '-0.007732', '-0.01546', '0.02632', '-0.01389', '0.01301', '0.002798', '-0.0111', '-0.000962', '-0.005726', '-0.01578', '0.00966', '-0.007393', '0.01614', '0.01941', '-0.0084', '-0.000524', '-0.0049', '-0.002747', '0.004616', '-0.02803', '0.00945', '-0.02434', '0.01313', '-0.002073', '-0.01465', '-0.00988', '0.01165', '0.004387', '0.00625', '0.02187', '-0.00921', '-0.01239', '0.003683', '0.004753', '-0.02612', '0.00437', '0.0184', '-0.001563', '-0.01671', '0.001228', '0.01417', '0.01077', '0.01779', '0.006004', '-0.00803', '0.002516', '0.02205', '0.009735', '-0.014534', '0.01336', '-0.01434', '-0.0004783', '-0.004673', '-0.01915', '0.00833', '0.02054', '0.01749', '0.004166', '-0.010025', '-0.01834', '-0.010475', '-0.007168', '-0.0078', '0.02193', '0.004593', '-0.009346', '0.01791', '0.01122', '0.02164', '0.0168', '0.01076', '0.01359', '0.005657', '-4.905e-05', '0.05136', '0.01881', '0.00972', '-0.01776', '-0.005505', '0.012115']",C129974,,C564127,277.2,,,
mondo:0013462,fucosyltransferase 6 deficiency,['fucosyltransferase 6 deficiency'],,613852,,C3151219,,,,,,,,
mondo:0013463,"congenital heart defects, multiple types, 6","['DTGA3', 'transposition of the great arteries, dextro-looped 3', 'dextro-looped transposition of the great arteries caused by mutation in GDF1', 'dextro-looped transposition of the great arteries 3', 'CHTD6', 'congenital heart defects, multiple types, 6', 'dextro-looped transposition of the great arteries type 3', 'transposition of the great arteries, dextro-looped type 3', 'transposition of the great arteries, dextro-looped 3, formerly', 'GDF1 dextro-looped transposition of the great arteries']",0060772,613854,,C3151221,,,,,,,,
mondo:0013464,episodic ataxia type 5,"['CACNB4 hereditary episodic ataxia', 'hereditary episodic ataxia caused by mutation in CACNB4', 'EA5', 'episodic ataxia, type 5']",0050993,613855,211067,C1866039,"['-0.2355', '-0.2354', '0.05673', '0.1482', '-0.1709', '-0.9634', '0.1057', '0.07404', '-0.85', '-1.107', '0.2532', '0.183', '-0.2104', '0.405', '0.736', '-0.2908', '-0.102', '-0.293', '0.0878', '-0.9004', '-0.1671', '-0.509', '0.185', '-0.8066', '0.494', '-0.629', '-0.3809', '0.2847', '-0.2449', '-0.9893', '0.05743', '0.5786', '-0.5205', '-0.0648', '0.2455', '0.1799', '-0.1552', '0.09937', '0.4673', '0.4993', '0.3865', '0.1461', '-0.3706', '0.2173', '0.6562', '-0.601', '0.12244', '0.3013', '0.6006', '0.00814', '-0.08746', '0.10266', '-0.1311', '-0.3718', '-0.1078', '-0.8447', '0.376', '0.626', '-0.1091', '0.4026', '-0.669', '0.2314', '0.2314', '-0.2334', '-0.535', '0.566', '0.2076', '0.5073', '-0.4265', '0.5186', '0.8184', '0.4292', '0.01172', '-0.877', '0.7627', '0.3962', '0.1846', '0.1628', '0.09674', '0.5103', '-0.292', '-1.009', '0.448', '0.7764', '-0.1309', '-0.8955', '0.1317', '-0.006344', '0.6094', '0.551', '0.1906', '0.537', '0.1512', '-0.07544', '1.173', '1.144', '0.2964', '0.4827', '-0.4102', '-0.1414']",,,C566601,,,,
mondo:0013465,achromatopsia 4,"['GNAT2 achromatopsia', 'achromatopsia caused by mutation in GNAT2', 'achromatopsia type 4', 'ACHM4', 'achromatopsia 4']",0110010,613856,,C1841721,,,,C564206,,,,
mondo:0013466,orofacial cleft 13,"['OFC13', 'orofacial cleft 13']",0080406,613857,,C3151222,,,,,,,,
mondo:0013467,immunodeficiency due to ficolin3 deficiency,"['ficolin 3 deficiency', 'lectin complement activation pathway, defect in, 3', 'immunodeficiency due to ficolin 3 deficiency', 'Fcn3 deficiency']",,613860,331190,C3151226,"['-0.1394', '0.2229', '-0.10443', '-0.1718', '0.0743', '-0.275', '0.0654', '-0.0845', '-0.05423', '0.1924', '0.00215', '0.2233', '-0.0641', '0.2886', '0.008934', '-0.1779', '0.1715', '0.2411', '-0.2815', '-0.5664', '0.2876', '-0.3254', '0.851', '-0.02081', '-0.02214', '0.09406', '-0.05157', '0.162', '-0.0877', '-0.2815', '0.3286', '0.08026', '0.3333', '0.1477', '0.02295', '-0.3535', '-0.0979', '0.307', '-0.01862', '-0.324', '-0.2463', '0.1704', '0.2037', '-0.3416', '-0.3098', '-0.3936', '0.2374', '-0.2834', '-0.2627', '0.4495', '-0.0673', '-0.1881', '0.3662', '-0.09045', '-0.4822', '0.3208', '0.1902', '-0.4001', '-0.1896', '0.0862', '0.0786', '0.4736', '-0.0372', '-0.05234', '0.4675', '0.05148', '0.4202', '0.2455', '-0.488', '0.461', '-0.2605', '0.05716', '-0.1051', '0.0569', '-0.01581', '-0.3816', '0.432', '0.01604', '0.2441', '0.11914', '-0.125', '-0.0603', '0.1708', '0.2485', '-0.3884', '-0.0692', '0.3547', '0.014206', '0.3647', '-0.05603', '0.536', '0.2874', '-0.1455', '-0.1375', '0.541', '0.6045', '0.1785', '-0.3936', '-0.1952', '0.0277']",,,,,,,
mondo:0013468,retinitis pigmentosa 59,"['RP59', 'retinitis pigmentosa type 59', 'retinitis pigmentosa caused by mutation in DHDDS', 'congenital disorder of glycosylation, type Ibb', 'congenital disorder of glycosylation, type 1bb', 'retinitis pigmentosa 59', 'DHDDS retinitis pigmentosa']",0110352,613861,,C3151227,,,,,,H35.5,,
mondo:0013469,retinitis pigmentosa 38,"['RP38', 'MERTK retinitis pigmentosa', 'Rod-cone dystrophy, childhood-onset', 'retinitis pigmentosa type 38', 'retinitis pigmentosa 38', 'retinitis pigmentosa caused by mutation in MERTK']",0110367,613862,,C3151228,,,,,,H35.5,,
mondo:0013470,"generalized epilepsy with febrile seizures plus, type 7","['generalized epilepsy with febrile seizures plus, type 7', 'generalised epilepsy with febrile seizures plus caused by mutation in SCN9A', 'Gefs+, type 7', 'SCN9A generalised epilepsy with febrile seizures plus', 'GEFSP7', 'generalized epilepsy with febrile seizures plus caused by mutation in SCN9A', 'febrile seizures, familial, 3B', 'SCN9A generalized epilepsy with febrile seizures plus']",0111295,613863,,,,,,C567827,,,,
mondo:0013471,autosomal recessive nonsyndromic hearing loss 61,"['autosomal recessive nonsyndromic deafness caused by mutation in SLC26A5', 'SLC26A5 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness 61', 'autosomal recessive deafness 61', 'deafness, autosomal recessive type 61', 'autosomal recessive nonsyndromic deafness type 61', 'deafness, autosomal recessive 61', 'DFNB61']",0110513,613865,,C3151230,,,,,,,,
mondo:0013472,fatal infantile hypertonic myofibrillar myopathy,"['alpha-B crystalin-related fatal infantile hypertonic myofibrillar myopathy', 'MFM, fatal infantile hypertonic, alpha-B crystallin-related', 'myopathy, myofibrillar, fatal infantile hypertonic, alpha-B crystallin-related', 'fatal infantile hypertonic myofibrillar myopathy', 'myofibrillar myopathy type 7']",0080309,613869,280553,C3151236,"['-0.525', '0.147', '-0.0768', '-0.2837', '-0.0895', '-0.4707', '0.0914', '0.695', '-0.5234', '0.05768', '-0.402', '0.10803', '-0.094', '-0.1412', '0.2186', '0.0672', '-0.07135', '-0.0769', '-0.1846', '-0.8076', '0.3306', '-0.0743', '0.2227', '0.07837', '-0.01029', '-0.0401', '0.2013', '-0.03723', '-0.303', '-0.05127', '0.2191', '0.3691', '0.4204', '0.3496', '0.01848', '-0.0802', '-0.04068', '-0.1693', '0.06226', '-0.2478', '-0.1761', '-0.3833', '0.01974', '0.2091', '-0.353', '0.1107', '-0.277', '0.2576', '-0.1759', '0.33', '-0.175', '0.1826', '0.02176', '-0.2135', '-0.01074', '-0.555', '0.1163', '-0.445', '0.1282', '0.04404', '0.384', '0.2915', '-0.02037', '-0.1648', '-0.273', '-0.1484', '0.4272', '0.5127', '-0.3137', '0.1991', '-0.1418', '0.04953', '0.1218', '-0.01439', '0.0232', '-0.1511', '-0.05478', '0.0789', '-0.16', '-0.04285', '0.1929', '0.2659', '-0.013985', '0.1354', '-0.05972', '0.2194', '0.0829', '0.1667', '0.3896', '-0.1556', '0.5083', '0.2156', '0.02228', '0.2208', '0.1664', '0.3584', '0.548', '-0.2251', '0.02913', '0.0963']",,,,,,,
mondo:0013473,"Hirschsprung disease, cardiac defects, and autonomic dysfunction","['HCAD', 'Hirschsprung disease, CARDIAC defects, and autonomic dysfunction', 'Hirschsprung disease, cardiac defects, and autonomic dysfunction']",,613870,,C3151237,,,,C563939,,,,
mondo:0013474,hypertrophic cardiomyopathy 17,"['cardiomyopathy, familial hypertrophic, 17', 'cardiomyopathy familial hypertrophic 17', 'cardiomyopathy, familial hypertrophic, type 17', 'JPH2 hypertrophic cardiomyopathy', 'cardiomyopathy, hypertrophic, 17', 'hypertrophic cardiomyopathy caused by mutation in JPH2', 'hypertrophic cardiomyopathy type 17', 'CMH17']",0110323,613873,,C3151264,,,,,,,,
mondo:0013475,hypertrophic cardiomyopathy 18,"['hypertrophic cardiomyopathy caused by mutation in PLN', 'cardiomyopathy, familial hypertrophic, 18', 'cardiomyopathy familial hypertrophic 18', 'cardiomyopathy, familial hypertrophic, type 18', 'PLN hypertrophic cardiomyopathy', 'hypertrophic cardiomyopathy type 18', 'cardiomyopathy, hypertrophic, 18', 'CMH18']",0110324,613874,,C3151265,,,,,,,,
mondo:0013476,hypertrophic cardiomyopathy 19,"['hypertrophic cardiomyopathy caused by mutation in CALR3', 'CALR3 hypertrophic cardiomyopathy', 'CMH19', 'hypertrophic cardiomyopathy type 19', 'cardiomyopathy, familial hypertrophic, 19', 'cardiomyopathy, familial hypertrophic, type 19', 'cardiomyopathy familial hypertrophic 19']",0110325,613875,,C3151266,,,,,,,,
mondo:0013477,hypertrophic cardiomyopathy 20,"['cardiomyopathy, familial hypertrophic, type 20', 'hypertrophic cardiomyopathy type 20', 'cardiomyopathy, hypertrophic, 20', 'NEXN hypertrophic cardiomyopathy', 'cardiomyopathy familial hypertrophic 20', 'cardiomyopathy, familial hypertrophic, 20', 'CMH20', 'hypertrophic cardiomyopathy caused by mutation in NEXN']",0110326,613876,,C3151267,,,,,,,,
mondo:0013478,PLIN1-related familial partial lipodystrophy,"['familial partial lipodystrophy type 4', 'lipodystrophy, familial partial, associated with Plin1 mutations', 'FPLD due to PLIN1 mutations', 'lipodystrophy, familial partial, type 4', 'FPLD4', 'PLIN1-related FPLD', 'familial partial lipodystrophy associated with PLIN1 mutations']",0070205,613877,280356,C3151268,"['-0.238', '0.2272', '0.2566', '-0.2727', '0.1076', '-0.3037', '0.1433', '0.3496', '-0.12256', '-0.1711', '-0.2522', '-0.225', '-0.10547', '-0.1012', '-0.2078', '-0.0908', '0.2727', '-0.041', '-0.11835', '-0.3743', '0.0379', '-0.3562', '0.3474', '0.11163', '-0.005486', '0.3193', '0.08276', '-0.06415', '0.0369', '-0.2932', '0.607', '0.1593', '0.2017', '0.04068', '0.08057', '-0.04794', '-0.01444', '0.1456', '-0.05557', '-0.3303', '-0.12286', '-0.3508', '0.04413', '0.273', '0.0825', '-0.0201', '0.0859', '0.2163', '0.1183', '-0.003706', '-0.221', '0.04422', '0.2822', '0.1888', '-0.4016', '-0.141', '0.2527', '-0.4016', '-0.2223', '0.0297', '0.1445', '0.04916', '0.0731', '-0.1432', '-0.2615', '0.001855', '0.0987', '0.2141', '-0.296', '0.1444', '-0.3013', '0.0617', '0.3186', '0.157', '0.1581', '-0.2045', '0.0988', '0.0852', '-0.10535', '-0.2378', '-0.1367', '0.2286', '0.1678', '-0.02748', '-0.1418', '0.1141', '0.10974', '0.2544', '0.3372', '0.1453', '0.2773', '0.02762', '-0.003483', '-0.01548', '0.4377', '-0.3088', '0.384', '-0.3079', '-0.2053', '0.292']",,,,,,,
mondo:0013479,dilated cardiomyopathy 1HH,"['cardiomyopathy, dilated, 1HH', 'CMD1HH', 'familial isolated dilated cardiomyopathy caused by mutation in BAG3', 'BAG3 familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 1HH', 'cardiomyopathy, dilated, type 1Hh']",0110448,613881,,C3151293,,,,,,,,
mondo:0013480,renal hypomagnesemia 6,"['hypomagnesemia 6, renal', 'HOMG6', 'renal hypomagnesemia-6', 'renal hypomagnesemia type 6']",0060884,613882,,C3151295,,,,,,,,
mondo:0013481,chromosome 13q14 deletion syndrome,"['chromosome 13q14 deletion syndrome', 'Del(13)(q14)', 'deletion 13q14', 'monosomy type 13q14', 'del(13q14)', 'monosomy 13q14', 'chromosome 13Q deletion syndrome', 'chromosome 13q14 deletion syndrome, isolated cases']",0060391,613884,1587,,,C36421,,C535484,,,,
mondo:0013482,"Meckel syndrome, type 8","['Meckel-Gruber syndrome, type 8', 'Meckel syndrome 8', 'Meckel syndrome, type 8', 'Meckel syndrome caused by mutation in TCTN2', 'MKS8', 'TCTN2 Meckel syndrome']",0070122,613885,90674,C3836857,,,,,,,,
mondo:0013483,"obesity, hyperphagia, and developmental delay","['OBHD', 'obesity, hyperphagia, and developmental delay']",,613886,,C3151303,"['-0.07404', '0.09467', '0.07074', '-0.01738', '0.0316', '-0.1489', '0.04312', '0.2076', '-0.1117', '-0.0696', '-0.05026', '-0.02602', '0.0524', '0.00602', '-0.0826', '-0.06097', '0.01706', '0.005264', '-0.0897', '-0.2212', '0.05002', '-0.03214', '0.06177', '-0.03864', '0.03625', '-0.06143', '0.001181', '-0.015564', '0.02536', '-0.10254', '0.11786', '-0.02632', '0.1976', '0.1011', '-0.000655', '-0.015076', '-0.02365', '-0.04547', '-0.058', '-0.11847', '0.06137', '-0.05542', '0.000823', '0.02774', '-0.01411', '-0.105', '0.02237', '0.0541', '-0.00824', '0.05096', '-0.0962', '0.01241', '0.0046', '0.04385', '-0.003347', '0.0181', '0.0367', '-0.03079', '-0.12274', '-0.02174', '0.06094', '0.03998', '-0.02097', '-0.01593', '0.008194', '0.02135', '0.02684', '0.12164', '-0.09674', '0.1217', '-0.08527', '0.04306', '0.0394', '-0.04538', '0.0177', '0.003162', '0.02586', '-0.02872', '-0.0957', '-0.010574', '-0.0051', '0.0111', '-0.06323', '0.07074', '0.0424', '0.05942', '0.02199', '0.10406', '0.2067', '0.0712', '0.0493', '0.1516', '-0.02524', '0.02707', '0.1604', '0.03001', '0.09753', '-0.1271', '0.03088', '0.03214']",,,C563938,,,,
mondo:0013484,cataract 36,"['cataract 36', 'cataract, autosomal recessive congenital 4', 'cataract type 36', 'CTRCT36', 'autosomal recessive congenital cataract 4', 'CATC4', 'TDRD7 cataract (disease)']",0110247,613887,,C3151304,,,,,,,,
mondo:0013485,spinocerebellar ataxia type 35,"['SCA35', 'spinocerebellar ataxia type 35', 'spinocerebellar ataxia 35']",0050982,613908,276193,CN202597,"['-0.04413', '-0.1763', '-0.1758', '0.0404', '-0.1163', '-0.6836', '0.2358', '0.32', '-0.6245', '-0.9766', '0.1324', '0.1681', '-0.1621', '0.2747', '0.5913', '-0.282', '-0.2404', '-0.428', '0.1364', '-0.9634', '-0.11395', '-0.4553', '-0.006893', '-0.5054', '0.1606', '-0.661', '-0.4983', '0.1395', '-0.1294', '-0.8467', '0.2119', '0.4475', '-0.4702', '-0.2727', '0.3594', '0.111', '-0.0709', '0.03214', '0.426', '0.469', '0.5923', '0.1902', '-0.2396', '0.559', '0.4507', '-0.6265', '0.0843', '0.262', '0.4014', '-0.3123', '-0.1703', '0.0867', '0.147', '-0.593', '-0.12', '-0.5845', '0.3706', '0.517', '-0.09875', '0.3726', '-0.394', '0.3623', '0.2235', '-0.0998', '-0.3752', '0.2266', '0.2452', '0.4688', '-0.5547', '0.3691', '0.635', '0.4612', '-0.1793', '-0.7188', '0.8975', '0.3958', '0.2595', '0.2234', '-0.0545', '0.4895', '-0.00555', '-0.7915', '0.504', '0.702', '-0.288', '-0.5312', '0.00981', '0.1544', '0.5923', '0.358', '0.371', '0.3691', '-0.00957', '-0.0516', '0.8477', '1.017', '0.5674', '0.4028', '-0.2325', '-0.01397']",,,,,,,
mondo:0013486,spinocerebellar ataxia type 32,"['cerebellar ataxia with azoospermia and intellectual disability', 'SCA32', 'spinocerebellar ataxia 32']",,613909,276183,C4304844,,,,,,,,
mondo:0013487,recurrent Neisseria infections due to factor D deficiency,"['factor D deficiency', 'CFDD', 'complement factor D deficiency']",,613912,169467,C0398764,"['-0.1909', '0.593', '-0.4036', '0.01396', '-0.2805', '0.1921', '0.1846', '-0.4365', '-0.1282', '-0.4124', '-0.2378', '0.2913', '-0.2455', '0.2021', '-0.0444', '-0.08844', '-0.1343', '0.2279', '-0.5137', '-0.631', '0.2349', '-0.528', '0.876', '-0.1746', '0.325', '0.2834', '0.00797', '-0.1003', '-0.3806', '-0.2284', '0.2402', '0.461', '0.2483', '0.3127', '-0.2462', '0.1273', '-0.2517', '-0.1669', '-0.3892', '-0.02455', '-0.2886', '0.11774', '0.2659', '-0.2386', '-0.0519', '-0.6924', '-0.041', '-0.305', '0.00224', '0.951', '-0.1242', '-0.1638', '0.1333', '-0.010506', '-0.4626', '-0.2096', '0.00958', '-0.3247', '0.0643', '0.2917', '0.04742', '0.4934', '-0.0199', '0.2201', '0.4343', '0.2542', '0.6245', '0.2856', '-0.3137', '0.4458', '-0.55', '-0.1746', '-0.007267', '-0.3823', '0.2249', '0.015564', '0.3604', '0.3557', '0.328', '-0.1389', '0.03708', '-0.359', '0.3997', '0.3608', '-0.2048', '-0.1189', '0.0615', '0.004074', '0.3247', '0.04083', '0.4758', '0.2598', '-0.1285', '-0.2015', '0.3198', '0.8735', '0.10144', '-0.5664', '-0.4543', '-0.0602']",,,C565027,279.8,,,
mondo:0013488,"lipodystrophy, partial, acquired, with low complement component c3, with or without glomerulonephritis","['lipodystrophy, partial, acquired, associated with C3 nephritic Factor', 'APLDC3', 'lipodystrophy, partial, acquired, with LOW complement component C3, with or without glomerulonephritis']",,613913,,C3151347,,,,,,,,
mondo:0013489,autosomal recessive nonsyndromic hearing loss 89,"['autosomal recessive deafness 89', 'deafness, autosomal recessive 89', 'DFNB89', 'deafness, autosomal recessive type 89', 'autosomal recessive nonsyndromic deafness 89', 'autosomal recessive nonsyndromic deafness type 89', 'autosomal recessive nonsyndromic deafness caused by mutation in KARS', 'KARS autosomal recessive nonsyndromic deafness']",0110534,613916,,C3151351,,,,,,,,
mondo:0013490,megalencephalic leukoencephalopathy with subcortical cysts 2A,"['megalencephalic leukoencephalopathy with subcortical cysts type 2A', 'MLC2A', 'megalencephalic leukoencephalopathy with subcortical cysts 2A']",0080318,613925,,C3151355,,,,,,,,
mondo:0013491,"megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability","['megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without mental retardation', 'megalencephalic leukoencephalopathy with subcortical cysts 2B, remitting, with or without intellectual disability', 'MLC2B']",0080317,613926,,C3151356,,,,,,,,
mondo:0013492,alopecia-intellectual disability syndrome 3,"['alopecia-intellectual disability syndrome 3', 'APMR3', 'alopecia-mental retardation syndrome 3']",0080951,613930,,C3151362,,,,,,,,
mondo:0013493,acetyl-coa carboxylase deficiency,"['ACETYL-CoA carboxylase deficiency', 'ACACAD', 'Acc1 deficiency', 'Acaca deficiency']",,613933,,C0268603,,,,C562678,,,,
mondo:0013495,autosomal recessive congenital ichthyosis 8,"['autosomal recessive congenital ichthyosis type 8', 'ichthyosis, congenital, autosomal recessive 8', 'late-onset lamellar ichthyosis', 'ichthyosis, congenital, autosomal recessive type 8', 'ichthyosis, lamellar, 4', 'ichthyosis, lamellar, 4, formerly', 'lamellar ichthyosis, late-onset', 'ARCI8', 'lamellar ichthyosis 4']",0060717,613943,,,,,,,,,,
mondo:0013496,"IgA nephropathy, susceptibility to, 2","['IGAN2', 'IgA nephropathy, susceptibility to, 2']",,613944,,,,,,,,,,
mondo:0013497,Okt4 epitope deficiency,"['Okt4 epitope deficiency', 'T4 epitope deficiency']",,613949,,C3151379,"['-0.004227', '-0.0008774', '0.00615', '0.00288', '-0.004463', '-0.005695', '-0.006542', '0.009346', '0.001373', '0.003817', '-0.001244', '-0.0029', '-0.0009522', '0.00952', '-0.011894', '-0.001316', '0.00441', '-0.0101', '-0.01065', '-0.022', '0.00562', '-0.014', '0.01894', '-0.01061', '0.009964', '-0.01122', '0.00309', '-0.00727', '-0.004044', '-1.866e-05', '0.001751', '0.0002503', '0.01162', '0.005573', '-0.002123', '-0.01074', '-0.001783', '-0.007183', '-0.002058', '-0.002417', '0.000747', '-0.02098', '0.002197', '0.00966', '0.00787', '-0.00931', '0.01062', '-0.00718', '0.01074', '0.00897', '-0.010796', '0.004395', '0.002232', '0.000839', '-0.0005255', '-0.001622', '0.00691', '0.00613', '-0.01193', '0.00653', '0.005344', '0.00906', '0.012085', '0.009476', '0.0111', '0.005543', '0.00747', '-0.0008664', '-0.001963', '-0.000287', '-0.00309', '0.00768', '0.00893', '0.0011215', '0.005962', '0.01369', '-0.007256', '-0.00841', '-0.01204', '-0.003832', '0.001078', '-0.00468', '0.00821', '0.00578', '-0.003668', '0.01004', '0.01047', '0.007298', '0.005764', '-0.00586', '0.005352', '0.01755', '0.006664', '-0.00566', '0.02293', '0.0153', '0.01263', '-0.00796', '-0.003899', '0.00794']",,,,,,,
mondo:0013498,schizophrenia 15,"['schizophrenia 15', 'schizophrenia type 15', 'schizophrenia susceptibility locus, chromosome 22Q13-related', 'SCZD15', 'schizophrenia 15 with or without an affective disorder']",0070091,613950,,C3151380,,,,,,,,
mondo:0013499,Fanconi anemia complementation group P,"['Slx4 Fanconi anaemia', 'Fanconi anaemia complementation group type P', 'Fanconi anaemia caused by mutation in Slx4', 'Fanconi Anemia, complementation group type P', 'Fanconi anaemia caused by mutation in SLX4', 'SLX4 Fanconi anaemia', 'SLX4 Fanconi anemia', 'Fanconi anemia caused by mutation in Slx4', 'Slx4 Fanconi anemia', 'FANCP', 'Fanconi anemia, complementation group P', 'Fanconi anemia complementation group type P']",0111092,613951,,,,,,,,,,
mondo:0013500,immunodeficiency 51,"['candidiasis, familial, type 5', 'candidiasis, familial, 5, formerly', 'immunodeficiency 51', 'IMD51', 'candidiasis, familial, 5', 'candidiasis, familial chronic mucocutaneous, autosomal recessive', 'CANDF5']",0111996,613953,1334,C4310803,"['-0.009995', '0.01962', '0.001797', '-0.003065', '0.02994', '-0.01529', '0.0006323', '0.02525', '-0.01884', '-0.003975', '-0.01303', '0.001151', '-0.013', '0.002605', '-0.010704', '-0.02135', '0.00689', '-0.02486', '-0.01164', '-0.066', '-0.01967', '-0.01179', '0.02164', '-0.0159', '0.01862', '-0.01926', '-0.01529', '-0.01028', '0.007835', '-0.02231', '0.02002', '0.002285', '0.0428', '0.0085', '0.01318', '-0.0142', '-0.014305', '-0.011154', '-0.006756', '-0.04028', '0.01564', '-0.03038', '0.003725', '-0.02809', '-0.010475', '-0.03014', '-0.01152', '0.01457', '0.00436', '0.01437', '-0.006496', '-0.00512', '-0.000489', '0.00985', '-0.01399', '-0.00972', '0.03033', '-0.02127', '-0.02242', '0.004574', '0.0253', '0.01332', '-4.48e-05', '0.010445', '0.012634', '0.0004718', '0.02364', '0.01532', '-0.01656', '0.01848', '-0.003014', '-0.010796', '0.00634', '-0.02231', '0.01653', '0.02278', '0.00714', '-0.01102', '-0.0096', '-0.005085', '1.15e-05', '-0.00839', '-0.0108', '0.0341', '-0.001953', '0.0045', '0.01067', '0.01842', '0.0451', '-0.00766', '0.007492', '0.01397', '-0.002031', '0.00418', '0.05658', '0.02316', '0.0359', '-0.04083', '-0.005188', '0.01358']",,,,,,,
mondo:0013501,frontotemporal dementia and/or amyotrophic lateral sclerosis 6,"['amyotrophic lateral sclerosis, with or without frontotemporal dementia', 'amyotrophic lateral sclerosis caused by mutation in VCP', 'VCP amyotrophic lateral sclerosis']",0060205,613954,,C3151403,,,,,,,,
mondo:0013502,"amyloidosis, primary localized cutaneous, 2","['PLCA2', 'amyloidosis, primary localised cutaneous, type 2', 'amyloidosis, primary localized cutaneous, 2', 'amyloidosis, primary localized cutaneous, type 2']",0080931,613955,,C3151404,,,,,,,,
mondo:0013503,"candidiasis, familial, 6","['candidiasis, familial, type 6', 'IL17F familial chronic mucocutaneous candidiasis', 'candidiasis, familial, 6', 'candidiasis, familial chronic mucocutaneous, autosomal dominant', 'CANDF6', 'candidiasis, familial, 6, autosomal dominant', 'familial chronic mucocutaneous candidiasis caused by mutation in IL17F']",,613956,,C3151405,,,,,,,,
mondo:0013504,spermatogenic failure 8,"['spermatogenic failure type 8', 'SPGF8', 'NR5A1 azoospermia', 'azoospermia caused by mutation in NR5A1', 'spermatogenic failure 8']",0070169,613957,,C3151406,,,,,,,,
mondo:0013505,spermatogenic failure 9,"['azoospermia caused by mutation in DPY19L2', 'globozoospermia, complete', 'SPGF9', 'DPY19L2 azoospermia', 'globozoospermia, total', 'spermatogenic failure type 9', 'spermatogenic failure 9']",0111156,613958,,C3151407,,,,,,,,
mondo:0013506,schizophrenia 16,"['schizophrenia susceptibility locus, chromosome 7Q36.3-related', 'schizophrenia type 16', 'schizophrenia 16', 'SCZD16', 'chromosome 7Q36.3 Duplication syndrome, 362-Kb']",0070092,613959,,C3151408,,,,,,,,
mondo:0013507,"granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type 3","['granulomatous disease, chronic, autosomal recessive, cytochrome b-POSITIVE, type III', 'granulomatous disease, chronic, due to Ncf4 deficiency', 'CGD, autosomal recessive cytochrome B-positive, type 3', 'chronic granulomatous disease 3, autosomal recessive', 'CDG3']",0070194,613960,,C3151409,,,,,,,,
mondo:0013508,"myopia 19, autosomal dominant","['MYP19', 'myopia 19, autosomal dominant']",,613969,,C3151410,,,,,,,,
mondo:0013509,"intellectual disability, autosomal dominant 6","['autosomal dominant intellectual disability 6', 'mental retardation, autosomal dominant 6', 'intellectual disability, autosomal dominant type 6', 'autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN2B', 'GRIN2B autosomal dominant non-syndromic intellectual disability', 'mental retardation, autosomal dominant type 6', 'autosomal dominant non-syndromic intellectual disability 6', 'intellectual disability, autosomal dominant 6', 'mental retardation, autosomal dominant 6, with or without seizures', 'autosomal dominant mental retardation 6', 'MRD6', 'intellectual disability, autosomal dominant 6, with or without seizures', 'intellectual developmental disorder, autosomal dominant 6, with or without seizures']",0070036,613970,,C3151411,,,,,,,,
mondo:0013510,"melanoma, cutaneous malignant, susceptibility to, 6","['melanoma, cutaneous malignant, 6', 'CMM6', 'melanoma, cutaneous malignant, susceptibility to, type 6', 'melanoma, cutaneous malignant, susceptibility to, 6', 'susceptibility to cutaneous malignant melanoma 6']",,613972,,,,,,,,,,
mondo:0013511,"cyanosis, transient neonatal","['cyanosis, transient neonatal', 'TNCY']",,613977,,C3151421,"['-0.004204', '0.01037', '0.0001724', '-0.006813', '-0.00513', '-0.01846', '-0.006752', '0.0097', '-0.006138', '-0.001379', '-0.009315', '0.0004091', '0.007515', '-0.001502', '-0.01323', '-0.004032', '-0.001897', '-0.0014105', '-0.01305', '-0.0377', '0.00895', '-0.01318', '0.00668', '-0.01464', '0.011444', '-0.00877', '0.008804', '-0.003784', '0.005623', '-0.00491', '0.01778', '-0.0076', '0.02158', '0.013016', '-0.006752', '-0.00861', '-0.006893', '-0.00662', '-0.01168', '-0.009', '0.01271', '-0.02316', '0.012344', '0.006817', '0.003462', '-0.012955', '-0.01093', '0.00627', '0.006943', '0.02054', '0.000866', '0.004128', '0.003712', '-0.002974', '0.004013', '-0.011215', '0.002424', '-0.01021', '-0.0149', '0.00597', '0.005604', '0.0009646', '-0.00396', '0.003836', '0.0102', '-0.006413', '0.01973', '0.019', '-0.02437', '0.010414', '0.0001781', '0.0006742', '0.00103', '-0.01472', '0.001887', '0.01662', '0.01662', '-0.005016', '-0.00642', '-0.01338', '0.002909', '0.001934', '-0.01326', '0.005154', '0.00663', '0.01006', '-0.006004', '0.00545', '0.01175', '-0.006706', '0.01663', '0.0206', '-0.003433', '0.01123', '0.02023', '0.01752', '0.005333', '-0.01081', '0.008194', '-0.001317']",,,,,,,
mondo:0013512,hemoglobin H disease,"['HbH disease', 'Alpha-thalassemia, Hemoglobin H type', 'hemoglobin H disease, deletional', 'haemoglobin H disease, deletional and nondeletional', 'hemoglobin H disease', 'alpha thalassemia, hemoglobin H type', 'haemoglobin H disease, deletional', 'HEMOGLOBIN H disease', 'Hemoglobin H disease, Nondeletional', 'Hemoglobin H disease, Deletional', 'Haemoglobin H disease, Deletional', 'Alpha-thalassemia, Haemoglobin H type', 'HbH', 'hemoglobin H disease, deletional and nondeletional', 'Alpha-thalassemia intermedia', 'alpha-thalassemia intermedia', 'alpha thalassemia, haemoglobin H type', 'Haemoglobin H disease, Nondeletional']",0110031,613978,93616,C3161174,"['-0.069', '0.436', '-0.4722', '-0.5654', '0.324', '-0.11755', '-0.3108', '0.971', '-0.2751', '-0.2888', '-0.1967', '0.3286', '-0.1566', '0.04114', '-0.1926', '-0.597', '-0.767', '-0.4587', '-0.4424', '-0.7334', '0.2805', '-0.2457', '1.308', '-0.01654', '0.2825', '0.1838', '-0.003735', '-0.03433', '0.2083', '-0.2192', '-0.10956', '-0.554', '0.3916', '-0.1931', '-0.2422', '-0.01196', '-1.15', '-0.6567', '0.03105', '-0.2144', '0.1376', '-0.1982', '0.666', '-0.0943', '-0.007313', '-0.1493', '-0.1744', '-0.1241', '0.2373', '-0.4749', '0.4507', '-0.3623', '-0.1802', '0.1064', '0.0567', '0.1423', '0.07983', '-0.1582', '-0.1615', '0.8286', '-0.07745', '-0.173', '-0.2374', '-0.3772', '-0.168', '0.06168', '0.2803', '0.408', '-0.3223', '0.3628', '0.3582', '-0.2803', '-0.332', '0.2515', '0.1876', '0.11334', '0.3857', '-0.798', '0.216', '-0.08344', '-0.2418', '-0.5312', '-0.256', '-0.1189', '0.0928', '0.2234', '-0.003403', '0.2583', '0.3804', '-0.1356', '0.752', '0.001226', '-0.2769', '-0.4604', '0.5923', '0.974', '-0.1283', '-0.4006', '-0.2915', '-0.259']",C95504,,,282.49,,10063435,
mondo:0013513,"atrial fibrillation, familial, 9","['atrial fibrillation, familial, 9', 'ATFB9', 'KCNJ2 familial atrial fibrillation', 'atrial fibrillation, familial, type 9', 'familial atrial fibrillation caused by mutation in KCNJ2']",,613980,,C3151431,,,,,,,,
mondo:0013514,hypotrichosis 3,"['hypotrichosis simplex of the scalp 2', 'Htss2', 'hypotrichosis caused by mutation in KRT74', 'KRT74 hypotrichosis', 'hypt3', 'hypotrichosis type 3', 'hypotrichosis 3', 'HYPT3']",0110700,613981,,C3151432,,,,,,,,
mondo:0013515,osteogenesis imperfecta type 6,"['osteogenesis imperfecta, type VI', 'osteogenesis imperfecta type', 'OI type 6', 'OI type VI', 'SERPINFI- related osteogenesis imperfecta', 'osteogenesis imperfecta type VI', 'osteogenesis imperfecta, type 6', 'OI6', 'osteogenesis imperfecta caused by mutation in SERPINF1', 'SERPINF1 osteogenesis imperfecta']",0110350,613982,216820,C3279564,,,,C536047,,,,
mondo:0013516,retinitis pigmentosa 60,"['RP60', 'retinitis pigmentosa 60', 'retinitis pigmentosa type 60', 'retinitis pigmentosa caused by mutation in PRPF6', 'PRPF6 retinitis pigmentosa']",0110411,613983,,C3151434,,,,,,H35.5,,
mondo:0013517,beta-thalassemia HBB/LCRB,"['thalassemia, beta', 'thalassemia, hispanic gamma-delta-beta', 'beta-thalassemia']",,613985,,,"['-0.01596', '0.03763', '-0.00814', '-0.01009', '0.0207', '-0.011955', '-0.00864', '0.01115', '-0.006096', '-0.0252', '-0.013245', '-0.00922', '-0.00723', '0.00967', '-0.02415', '-0.01959', '-0.01913', '-0.00318', '-0.009125', '-0.02505', '-0.00665', '-0.01504', '0.02739', '-0.00814', '0.02145', '0.00291', '0.00801', '0.000401', '0.01391', '-0.02435', '-0.01039', '-0.011444', '0.0282', '0.01335', '-0.01049', '-0.014206', '-0.00868', '-0.01419', '-0.002527', '-0.01964', '0.0184', '-0.01532', '0.006596', '-0.008354', '-0.004116', '-0.01613', '-0.01581', '0.0221', '0.003727', '0.007164', '-0.01329', '-0.02577', '0.01209', '0.008736', '-0.02663', '0.003809', '0.02164', '-0.002089', '-0.01784', '-0.007626', '-4.834e-05', '-0.007156', '-0.01278', '0.02045', '0.0166', '0.0002137', '0.01547', '0.003237', '-0.00854', '0.02075', '-0.01371', '-0.006557', '-0.00524', '-0.01079', '0.012474', '0.00699', '0.00578', '-0.0152', '0.006508', '-0.01299', '-0.010864', '0.01372', '-0.01377', '-0.008224', '-0.02397', '0.00481', '0.01701', '0.0249', '0.01046', '-0.004425', '0.00786', '0.005215', '1.997e-05', '-0.00957', '0.03543', '0.0056', '0.007427', '-0.03812', '-0.01752', '-0.0005774']",,,,,,,
mondo:0013518,"pituitary hormone deficiency, combined, 6","['OTX2 combined pituitary hormone deficiencies, genetic form', 'CPHD6', 'pituitary hormone deficiency, combined, 6', 'combined pituitary hormone deficiencies, genetic form caused by mutation in OTX2', 'pituitary hormone deficiency, combined, type 6']",,613986,,C3151440,,,,,,,,
mondo:0013519,"dyskeratosis congenita, autosomal recessive 2","['DKCB2', 'dyskeratosis congenita, autosomal recessive type 2', 'dyskeratosis congenita, autosomal recessive 2', 'autosomal recessive dyskeratosis congenita 2']",0070017,613987,,C3151441,,C176926,,,,,,
mondo:0013520,"dyskeratosis congenita, autosomal recessive 3","['dyskeratosis congenita, autosomal recessive 3', 'DKCB3', 'autosomal recessive dyskeratosis congenita 3', 'dyskeratosis congenita, autosomal recessive type 3']",0070019,613988,,C3151442,,C176927,,,,,,
mondo:0013521,"dyskeratosis congenita, autosomal dominant 2","['dyskeratosis congenita, autosomal dominant 2', 'DKCA2', 'dyskeratosis congenita, autosomal dominant type 2', 'autosomal dominant dyskeratosis congenita 2', 'dyskeratosis congenita, autosomal recessive 4']",0070016,613989,3322,C3151443,,C176922,,,,,,
mondo:0013522,"dyskeratosis congenita, autosomal dominant 3","['dyskeratosis congenita, autosomal dominant 3', 'dyskeratosis congenita, autosomal dominant type 3', 'autosomal dominant dyskeratosis congenita 3', 'DKCA3']",0070018,613990,3322,C3151445,,C176923,,,,,,
mondo:0013523,Nestor-Guillermo progeria syndrome,"['Nestor-Guillermo progeria syndrome', 'PSCOO', 'NGPS', 'progeria syndrome, childhood-onset, with osteolysis']",0081334,614008,280576,C3151446,"['-0.1442', '0.1425', '0.2314', '0.2854', '0.3655', '-0.5957', '0.07605', '1.555', '-0.347', '-0.539', '0.07007', '-0.273', '0.627', '0.4883', '-0.1912', '0.2136', '0.5723', '-0.05994', '-0.26', '-0.3132', '-0.1022', '-0.4495', '0.04852', '-0.2566', '0.772', '0.4944', '0.1362', '0.6978', '0.2384', '0.1719', '0.4194', '-0.03912', '0.1967', '0.1765', '0.2462', '0.45', '-0.1897', '-0.2568', '0.02007', '-0.798', '0.478', '0.1461', '-0.2693', '-0.03595', '0.2126', '-0.4905', '0.0591', '-0.01695', '0.4998', '-0.3774', '-0.3447', '0.3264', '0.177', '0.2854', '-0.2617', '-1.124', '-0.5796', '0.3914', '0.2125', '0.1132', '-0.375', '0.085', '0.2483', '-0.539', '-0.1381', '0.4136', '0.511', '0.3313', '-0.594', '0.8237', '-0.4817', '0.1353', '0.4797', '0.2037', '-0.07935', '0.0003943', '-0.0775', '0.8013', '0.02052', '-0.1799', '-0.3164', '-0.08', '-0.354', '-0.2847', '0.05475', '-0.1213', '0.3635', '-0.09863', '0.6357', '0.375', '0.11847', '-0.04254', '0.4788', '0.49', '0.00674', '-0.010796', '0.22', '0.1293', '0.669', '-0.1339']",,,,,,,
mondo:0013524,bleeding diathesis due to thromboxane synthesis deficiency,"['bleeding disorder, platelet-type, 13, susceptibility to', 'BDPLT13', 'susceptibility to platelet-type bleeding disorder 13', 'bleeding disorder, susceptibility to, due to defective platelet thromboxane A2 receptor']",,614009,220443,,"['-0.5767', '-0.1555', '0.07556', '-0.3008', '0.0697', '0.1901', '-0.0968', '0.1376', '0.02191', '0.2131', '-0.1036', '0.1449', '0.182', '0.0477', '-0.3616', '-0.2219', '-0.05264', '-0.08185', '-0.1104', '-0.574', '-0.033', '-0.1161', '0.4902', '-0.2163', '-0.1255', '-0.2272', '0.01567', '0.03842', '0.1401', '-0.09674', '-0.0885', '0.2524', '0.2878', '0.361', '-0.0882', '-0.3762', '-0.1625', '-0.028', '-0.197', '-0.3167', '0.3386', '-0.122', '0.2241', '-0.237', '-0.3767', '-0.2056', '-0.08417', '0.00364', '0.286', '0.2081', '0.08234', '-0.183', '0.1705', '0.2615', '-0.2998', '0.0306', '0.2468', '-0.05304', '-0.5273', '0.011314', '0.0674', '0.1989', '0.01758', '-0.3274', '0.2472', '0.0651', '0.2698', '0.0723', '-0.162', '0.277', '-0.374', '-0.06235', '-0.10016', '-0.2712', '0.3557', '-0.1197', '0.6406', '-0.1006', '0.2388', '0.00963', '-0.4226', '-0.2422', '0.07666', '0.11707', '-0.1481', '0.1321', '0.2399', '0.2808', '0.4893', '-0.3872', '0.2034', '0.549', '0.0942', '-0.10345', '0.4316', '0.3345', '0.2688', '-0.4275', '0.1044', '0.4075']",,,,,,,
mondo:0013525,primary ciliary dyskinesia 16,"['CILD16', 'primary ciliary dyskinesia type 16', 'primary ciliary dyskinesia 16 with or without situs inversus', 'ciliary dyskinesia, primary, type 16', 'primary ciliary dyskinesia caused by mutation in DNAL1', 'ciliary dyskinesia, primary, 16', 'ciliary dyskinesia, primary, 16, with or without situs inversus', 'DNAL1 primary ciliary dyskinesia']",0110613,614017,,C3151460,,,,,,,,
mondo:0013526,progressive myoclonic epilepsy type 6,"['progressive myoclonus epilepsy type 6', 'GOSR2-related progressive myoclonus ataxia', 'epilepsy, progressive myoclonic 6', 'epilepsy, progressive myoclonic, type 6', 'epilepsy, progressive myoclonic, 6', 'progressive myoclonic epilepsy caused by mutation in GOSR2', 'PME type 6', 'EPM6', 'North Sea progressive myoclonus epilepsy', 'GOSR2 progressive myoclonic epilepsy']",0111449,614018,280620,C3279627,"['0.857', '0.307', '-0.3035', '-0.06915', '-0.516', '-0.3462', '0.739', '0.3547', '-0.809', '-0.453', '0.0469', '-0.3093', '-0.3738', '0.3918', '0.05978', '0.06195', '-0.2035', '-0.6', '-0.3035', '-0.5366', '-0.2319', '0.627', '-0.00935', '-0.495', '-0.2408', '-0.1472', '-0.05774', '-0.0531', '-0.4614', '0.3533', '0.2422', '-0.6943', '0.11707', '0.3198', '0.7344', '0.4014', '-0.10834', '0.05786', '-0.05154', '-0.3784', '-0.05588', '-0.446', '0.09216', '-0.3323', '-0.4878', '-0.792', '-0.3245', '0.297', '0.35', '0.703', '-0.2551', '0.1131', '0.11163', '-0.4932', '-0.01718', '-0.3052', '-0.08746', '0.1045', '-0.1593', '0.2261', '-0.708', '0.5737', '0.7837', '-0.437', '-0.4968', '1.41', '0.381', '-0.01188', '-1.02', '0.5596', '1.098', '1.024', '0.0904', '-0.4148', '0.09924', '0.713', '1.227', '0.3523', '-0.314', '0.4426', '-0.1261', '0.671', '0.426', '0.1527', '0.2754', '0.1565', '0.1948', '0.586', '0.7544', '0.4116', '0.0803', '0.1793', '-0.2333', '0.1008', '0.0992', '0.181', '0.2426', '-0.588', '0.332', '0.3074']",,,,,,,
mondo:0013527,lissencephaly 4,"['NDE1 lissencephaly (disease)', 'lissencephaly 4 (with microcephaly)', 'lissencephaly 4', 'LIS4', 'lissencephaly 4, with microcephaly', 'lissencephaly 4 with microcephaly', 'lissencephaly type 4']",0112235,614019,,C3151461,,,,,,,,
mondo:0013528,"intellectual disability, autosomal recessive 14","['MRT14', 'TECR autosomal recessive non-syndromic intellectual disability', 'autosomal recessive non-syndromic intellectual disability caused by mutation in TECR', 'intellectual disability, autosomal recessive 14', 'mental retardation, autosomal recessive type 14', 'intellectual disability, autosomal recessive type 14', 'mental retardation, autosomal recessive 14']",0081188,614020,,C3151462,,,,,,,,
mondo:0013529,catecholaminergic polymorphic ventricular tachycardia 3,"['catecholaminergic polymorphic ventricular tachycardia type 3', 'CVPT3', 'ventricular tachycardia, catecholaminergic polymorphic, 3', 'catecholaminergic polymorphic ventricular tachycardia caused by mutation in TECRL', 'CPVT3', 'TECRL catecholaminergic polymorphic ventricular tachycardia']",0060677,614021,,C3151463,,,,,,I47.2,,
mondo:0013530,"atrial fibrillation, familial, 10","['familial atrial fibrillation caused by mutation in SCN5A', 'atrial fibrillation, familial, 10', 'ATFB10', 'SCN5A familial atrial fibrillation', 'atrial fibrillation, familial, type 10']",,614022,,C3151464,,,,,,,,
mondo:0013531,PSPH deficiency,"['PSPHD', '3-phosphoserine phosphatase deficiency', 'phosphoserine phosphatase deficiency']",0050724,614023,79350,C1291463,"['-0.5093', '0.1676', '0.11084', '-0.1464', '0.1698', '-0.1812', '-0.2842', '0.4106', '-0.10376', '-0.516', '-0.18', '0.159', '-0.0313', '-0.2756', '-0.1483', '-0.04025', '0.235', '-0.1387', '-0.3833', '-0.7554', '0.0817', '-0.1415', '0.426', '-0.4255', '0.01929', '0.3276', '-0.183', '-0.0892', '0.2312', '-0.397', '-0.02925', '0.3044', '0.2678', '0.0859', '-0.3257', '-0.2312', '-0.1976', '-0.2578', '-0.2018', '-0.2103', '0.3293', '-0.482', '0.118', '-0.4487', '-0.03537', '0.01846', '0.1978', '0.1603', '-0.00731', '0.06158', '-0.07056', '-0.195', '-0.04996', '-0.05344', '-0.2786', '-0.502', '0.265', '-0.1886', '-0.4954', '0.4443', '0.22', '-0.166', '0.3027', '-0.335', '0.264', '-0.10095', '0.2942', '0.1334', '-0.719', '0.01772', '-0.2922', '0.2605', '0.2137', '-0.1273', '0.0501', '0.11926', '0.02408', '-0.2139', '-0.1261', '0.2186', '0.399', '0.2664', '-0.1937', '0.3455', '0.313', '0.0774', '0.1058', '0.252', '0.4714', '0.005898', '0.2666', '0.617', '-0.1532', '-0.1407', '0.6934', '0.3699', '0.1279', '-0.586', '0.3555', '-0.1333']",,,,277.6,,,
mondo:0013532,protein Z deficiency,"['protein z deficiency', 'protein Z deficiency']",,614024,,C3151465,,,,,,,,
mondo:0013533,hyperlipidemia due to hepatic triglyceride lipase deficiency,"['hyperlipidemia due to HL deficiency', 'lipc deficiency', 'hyperlipidemia due to hepatic lipase deficiency', 'hepatic lipase deficiency', 'hyperlipidemia due to hepatic triacylglycerol lipase deficiency', 'hyperlipidemia due to HTGL deficiency', 'HL deficiency']",,614025,140905,C3151466,"['-0.3738', '0.2306', '0.2786', '0.3923', '0.3125', '-0.1305', '-0.3274', '0.3826', '0.04813', '-0.09155', '0.1082', '-0.3413', '0.1602', '0.02348', '-0.669', '-0.5815', '0.1924', '0.2556', '-0.4487', '-0.748', '0.2554', '-0.4204', '0.7188', '0.2162', '0.1558', '0.33', '0.1846', '0.005928', '-0.0328', '-0.0881', '0.806', '0.06946', '0.5737', '0.10834', '-0.02162', '-0.6445', '-0.1364', '0.7236', '0.4297', '-0.939', '-0.169', '0.01323', '0.3188', '0.14', '-0.753', '-0.4204', '0.368', '0.173', '0.2444', '0.2632', '0.1628', '-0.554', '0.51', '-0.0972', '-0.2874', '0.3877', '-0.0705', '-0.563', '-0.726', '-0.05817', '-0.2966', '0.543', '0.43', '-0.74', '0.206', '0.2284', '-0.0429', '0.1475', '-0.7114', '-0.1826', '-0.1901', '0.012985', '0.3704', '0.3586', '-0.06055', '0.3486', '0.0348', '0.2413', '-0.1641', '-0.3403', '-0.3306', '-0.1447', '0.0739', '-0.02176', '0.0498', '0.02339', '0.2482', '0.1002', '0.5815', '0.3538', '0.142', '0.07104', '-0.348', '0.02116', '0.299', '0.363', '0.0991', '-0.6406', '-0.4749', '-0.06113']",,,,,,,
mondo:0013534,apolipoprotein c-III deficiency,"['apolipoprotein c-III deficiency', 'hyperalphalipoproteinemia 2']",0111370,614028,,C3151467,,,,C566270,,,,
mondo:0013535,hydroxyacyl glutathione hydrolase deficiency,"['glyoxalase II deficiency', 'glyoxalase 2 deficiency', 'hydroxyacyl glutathione hydrolase deficiency']",,614033,,C3279657,,,,C564215,,,,
mondo:0013536,heme oxygenase 1 deficiency,"['HMOX1D', 'heme oxygenase-1 deficiency', 'heme oxygenase 1 deficiency']",,614034,562509,C1841651,"['-0.02592', '0.01065', '-0.00728', '-0.006554', '0.00527', '-0.02522', '0.006187', '0.02835', '-0.01457', '-0.0169', '-0.01569', '0.00674', '0.0016165', '-0.00328', '-0.02647', '-0.02547', '-0.005157', '-0.000498', '-0.015', '-0.06244', '-0.01118', '-0.01805', '0.03818', '-0.02013', '7.63e-05', '-0.001926', '-0.006416', '2.7e-05', '0.003414', '-0.006603', '0.02155', '0.003443', '0.02138', '0.01384', '-0.00538', '-0.003174', '0.003857', '-0.006775', '-0.011154', '-0.02086', '0.01387', '-0.03', '0.02574', '-0.009895', '-0.0147', '-0.02538', '0.01058', '0.0108', '6.62e-05', '0.02187', '-0.003477', '-0.00954', '0.02365', '0.0172', '-0.02423', '-0.01455', '0.02646', '-0.01868', '-0.03128', '0.00667', '0.01863', '0.000298', '0.02171', '0.00372', '0.005665', '0.00824', '0.0281', '0.01149', '-0.02634', '0.01141', '-0.01218', '0.001632', '-0.00378', '-0.01991', '0.01591', '0.02774', '-0.000974', '-0.00787', '-0.00558', '-0.03546', '-0.0008664', '-0.01651', '-0.009796', '0.014145', '0.0008154', '0.002369', '0.015205', '0.03009', '0.02888', '0.00786', '0.01396', '0.01846', '-0.003096', '0.005253', '0.0642', '0.02278', '0.01266', '-0.03937', '-0.00168', '0.01704']",,,C564200,,,,
mondo:0013537,autosomal recessive nonsyndromic hearing loss 29,"['DFNB29', 'deafness, autosomal recessive type 29', 'autosomal recessive nonsyndromic deafness 29', 'CLDN14 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 29', 'deafness, autosomal recessive 29', 'autosomal recessive nonsyndromic deafness caused by mutation in CLDN14', 'autosomal recessive deafness 29']",0110487,614035,,C3279660,,,,,,,,
mondo:0013539,hypotonia-failure to thrive-microcephaly syndrome,"['LTC4 synthase deficiency', 'leukotriene C4 synthase deficiency']",,614037,79507,C3279662,,,,C565439,,,,
mondo:0013540,deafness-lymphedema-leukemia syndrome,"['Emberger syndrome', 'lymphedema, primary, with myelodysplasia']",,614038,3226,C3279664,"['0.816', '-0.2278', '-0.1469', '0.04932', '-0.0771', '-0.8584', '0.3306', '0.127', '-0.11755', '-0.6157', '0.3752', '1.187', '0.1528', '0.821', '-0.392', '0.276', '-0.2056', '-0.2227', '-0.1062', '-0.2427', '0.079', '-0.1008', '0.2673', '-0.003479', '0.2211', '-0.0695', '-0.2009', '0.6875', '0.442', '-0.2145', '-0.4255', '0.6465', '0.656', '-0.128', '0.3809', '0.1688', '-0.4216', '-0.3386', '0.6978', '-0.6', '0.1835', '0.521', '0.4827', '-0.04376', '-0.01095', '0.02945', '-0.5884', '-0.4773', '1.186', '-0.1925', '-0.0976', '-0.1277', '0.7773', '0.5054', '-0.5684', '-0.3484', '-0.2272', '-1.018', '-0.806', '-0.2808', '0.2996', '0.1917', '-0.2196', '-0.03427', '-0.573', '0.3687', '0.3735', '0.949', '-0.7236', '-0.1624', '-0.808', '0.2969', '-0.0517', '-0.3337', '0.3381', '0.06235', '-0.4038', '0.7715', '0.371', '-0.347', '-0.138', '0.7827', '-0.02374', '0.5444', '0.4924', '-0.2395', '-0.5566', '-0.435', '-0.1849', '0.0735', '-0.1675', '0.8696', '-0.1975', '0.2834', '1.222', '0.05283', '0.98', '-0.5005', '0.1454', '0.04633']",,,,757.0,,,
mondo:0013541,complex cortical dysplasia with other brain malformations 1,"['cortical dysgenesis with pontocerebellar hypoplasia due to TUBB3 mutation', 'complex cortical dysplasia with other brain malformations type 1', 'cortical dysplasia, complex, with other brain malformations 1', 'TUBB3 complex cortical dysplasia with other brain malformations', 'cortical dysplasia, Complex, with Other brain malformations type 1', 'CDCBM1', 'complex cortical dysplasia with other brain malformations caused by mutation in TUBB3']",0090137,614039,300570,CN203402,"['-0.4175', '0.206', '0.4856', '-0.2915', '0.1497', '-0.1663', '0.1991', '0.3113', '-0.465', '-0.1116', '-0.3884', '-0.493', '-0.339', '-0.5327', '0.2842', '-0.2827', '0.101', '-0.3774', '-0.3738', '-0.6343', '0.1718', '0.03418', '0.2366', '0.00755', '0.1758', '0.05624', '0.11127', '0.2886', '0.0849', '-0.0883', '0.12354', '0.1361', '0.8193', '0.05347', '0.3848', '-0.0893', '-0.1816', '-0.1487', '-0.0501', '-0.4524', '0.1747', '-0.3171', '-0.03644', '0.2046', '-0.2527', '-0.3567', '0.201', '0.1887', '-0.04526', '-0.4373', '0.3877', '0.1859', '-0.2213', '-0.1665', '-0.3713', '-0.1477', '0.3242', '0.02524', '-0.4285', '0.444', '-0.01889', '0.03403', '0.3008', '0.1139', '-0.551', '0.1072', '0.4067', '0.4412', '-0.3074', '0.3523', '-0.2698', '0.483', '0.26', '-0.06134', '-0.1649', '-0.2173', '0.5825', '-0.1274', '-0.4316', '0.1417', '-0.115', '0.06854', '0.2126', '0.572', '-0.03757', '-0.3264', '0.07666', '0.666', '0.3447', '0.05038', '0.2188', '0.2384', '0.01811', '-0.09204', '0.671', '0.0416', '0.683', '-0.05112', '0.6616', '0.329']",,,,,,,
mondo:0013542,Moyamoya disease 5,"['Moyamoya disease type 5', 'Moyamoya disease 5', 'ACTA2 Moyamoya disease', 'Moyamoya disease caused by mutation in ACTA2', 'MYMY5']",,614042,,C3279690,,,,,,,,
mondo:0013543,trypsinogen deficiency,['trypsinogen deficiency'],,614044,,C0268417,,,,,277.89,,,
mondo:0013544,"atrial fibrillation, familial, 11","['ATFB11', 'atrial fibrillation, familial, 11', 'atrial fibrillation, familial, type 11', 'GJA5 familial atrial fibrillation', 'familial atrial fibrillation caused by mutation in GJA5']",,614049,,C3279693,,,,,,,,
mondo:0013545,"atrial fibrillation, familial, 12","['ABCC9 familial atrial fibrillation', 'familial atrial fibrillation caused by mutation in ABCC9', 'ATFB12', 'atrial fibrillation, familial, type 12', 'atrial fibrillation, familial, 12']",,614050,,C3279695,,,,,,,,
mondo:0013546,mitochondrial complex V (ATP synthase) deficiency nuclear type 2,"['TMEM70 defect', 'neonatal mitochondrial encephalocardiomyopathy due to ATP synthase deficiency', 'mitochondrial Complex 5 (ATP synthase) deficiency, Tmem70 type', 'mitochondrial encephalo-cardio-myopathy due to F1Fo ATPase deficiency', 'MC5DN2', 'mitochondrial encephalo-cardio-myopathy due to isolated mitochondrial respiratory chain complex V deficiency', 'TMEM70-related mitochondrial encephalo-cardio-myopathy', '3-MGCA type IV (3-MGCA-4) (formerly)', 'encephalocardiomyopathy, mitochondrial, neonatal, due to ATP synthase deficiency', 'mitochondrial complex V (ATP synthase) deficiency, nuclear type 2', 'mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 2', 'mitochondrial encephalo-cardio-myopathy due to isolated ATP synthase deficiency']",0060331,614052,1194,,"['-0.3032', '0.5493', '-0.3853', '0.0751', '0.173', '-0.689', '0.1741', '1.2', '-0.514', '-0.2964', '0.0638', '-0.366', '0.5684', '-0.4304', '-0.3823', '0.10516', '0.3452', '-0.562', '-0.7075', '-0.6763', '0.4402', '-0.2522', '0.2712', '-0.005386', '0.0431', '-0.423', '-0.4907', '0.646', '0.3743', '0.1214', '0.2227', '0.3628', '0.57', '0.3406', '-0.526', '-0.335', '-0.03378', '0.4019', '0.02155', '0.1142', '0.03796', '0.1669', '0.2517', '0.4607', '-0.8223', '0.02965', '0.09155', '0.0942', '0.153', '-0.002518', '-0.634', '-0.7085', '-0.3723', '0.4749', '-0.0829', '-0.0261', '0.0423', '0.004353', '0.0882', '0.8213', '0.1471', '-0.10547', '0.506', '-0.726', '-0.11975', '0.00505', '0.634', '0.5293', '-0.655', '-0.01694', '-0.3674', '0.2068', '0.3699', '0.2886', '0.2744', '0.378', '0.5703', '-0.653', '-0.5977', '1.151', '0.4258', '-0.2651', '-0.4128', '-0.3223', '0.5645', '0.733', '0.10657', '0.1996', '0.5264', '0.0815', '0.1726', '0.4202', '0.2085', '0.1603', '0.5674', '0.571', '0.2369', '-0.6953', '0.003338', '-0.1654']",,,C567528,,,,
mondo:0013547,mitochondrial complex V (ATP synthase) deficiency nuclear type 3,"['mitochondrial complex V (ATP synthase) deficiency, nuclear type 3', 'mitochondrial proton-transporting ATP synthase complex deficiency caused by mutation in ATP5F1E', 'ATP5F1E mitochondrial proton-transporting ATP synthase complex deficiency', 'MC5DN3', 'mitochondrial Complex 5 (ATP synthase) deficiency, Atp5E type', 'mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 3']",0060332,614053,,C3279708,,,,,,,,
mondo:0013548,acetyl-CoA acetyltransferase-2 deficiency,"['ACETYL-CoA acetyltransferase-2 deficiency', 'Acetyl CoA acetyltransferase 2 deficiency', 'ACAT2', 'acetoacetyl CoA thiolase, cytosolic', 'ACAT2D', 'Acat2 deficiency', 'Acetocoenzyme A acetyltransferase 2', 'acetyl-CoA acetyltransferase-2 deficiency', 'ACAT2 deficiency, Isolated cases']",,614055,,C0342735,,,,C536005,,,,
mondo:0013549,N-acetylaspartate deficiency,"['naa deficiency', 'N-acetylaspartate deficiency', 'NACED', 'hypoacetylaspartia']",,614063,,C3279716,"['-0.04666', '0.0251', '-0.002552', '-0.007195', '0.02327', '-0.0465', '0.00871', '0.05634', '-0.03058', '-0.0241', '-0.01273', '-0.00786', '-0.003828', '0.00807', '-0.01933', '-0.01392', '0.00191', '-0.007095', '-0.0412', '-0.1187', '-0.000602', '-0.0438', '0.05072', '-0.01342', '0.0093', '-0.001367', '-0.003803', '-0.01714', '0.010735', '-0.03763', '0.0402', '0.00264', '0.0588', '0.02911', '-0.001327', '-0.05072', '-0.01764', '-0.03503', '-0.007065', '-0.05624', '0.03058', '-0.05313', '0.0358', '0.01128', '-0.011055', '-0.03854', '0.0097', '0.03415', '0.02115', '0.03622', '-0.02473', '-0.02522', '0.02174', '0.011215', '-0.0269', '-0.006706', '0.03452', '-0.00784', '-0.068', '0.005974', '0.01539', '0.01825', '0.02464', '0.00601', '0.02039', '0.02281', '0.04343', '0.0504', '-0.0647', '0.05228', '-0.03778', '-0.00266', '0.0002513', '-0.05832', '0.0329', '0.03278', '0.011795', '-0.006405', '-0.01654', '-0.003195', '-0.004837', '-0.01303', '-0.003033', '0.02579', '0.03314', '0.01198', '0.02194', '0.03662', '0.088', '0.02173', '0.02727', '0.04605', '-0.006313', '0.01161', '0.1073', '0.05966', '0.02968', '-0.0767', '0.002956', '0.02216']",,,,,,,
mondo:0013550,distal myopathy with posterior leg and anterior hand involvement,"['Williams distal myopathy', 'distal ABD-filaminopathy', 'myopathy, distal, type 4', 'MPD4', 'myopathy, distal, 4']",0111190,614065,63273,C4518807,"['-0.6157', '-0.1097', '-0.204', '-0.0504', '0.05173', '-0.756', '-0.03607', '0.7676', '-0.8975', '-0.632', '-0.2294', '0.02719', '-0.07776', '0.2087', '0.001558', '-0.2435', '-0.1454', '-0.07764', '-0.3977', '-0.8833', '0.1534', '-0.05182', '0.10126', '0.2908', '-0.05228', '0.1129', '-0.006588', '0.1442', '-0.5044', '0.02461', '0.503', '-0.0854', '-0.4075', '-0.1431', '0.1772', '-0.0743', '-0.1991', '-0.2656', '-0.0661', '0.02199', '-0.2776', '-0.538', '-0.1164', '0.3967', '-0.10876', '0.3354', '-0.2128', '0.0917', '0.06058', '0.005203', '0.1914', '0.1774', '0.04074', '-0.1201', '0.2167', '-0.994', '0.3337', '0.2161', '-0.003387', '0.1537', '0.1193', '-0.248', '0.1409', '0.2546', '-0.797', '0.3552', '0.3135', '0.724', '-0.635', '0.2487', '-0.0447', '-0.1367', '0.10913', '0.3042', '0.486', '0.1034', '-0.2896', '0.2744', '-0.247', '-0.3472', '0.1305', '0.2347', '0.842', '0.6343', '-0.04874', '0.11127', '-0.562', '0.1738', '0.539', '-0.681', '0.2129', '-0.02954', '0.4827', '0.1438', '0.635', '0.06726', '0.2751', '-0.4202', '-0.1624', '0.0945']",,,,,,,
mondo:0013551,hereditary spastic paraplegia 47,"['SPG47', 'hereditary spastic paraplegia caused by mutation in AP4B1', 'hereditary spastic paraplegia type 47', 'AP4B1 hereditary spastic paraplegia', 'cerebral palsy, spastic quadriplegic, 5, formerly', 'autosomal recessive spastic paraplegia 47', 'spastic paraplegia 47, autosomal recessive', 'spastic quadriplegic cerebral palsy 5', 'CPSQ5', 'cerebral palsy, spastic quadriplegic, 5']",0110799,614066,,C3279738,,C164224,,,,,,
mondo:0013552,hereditary spastic paraplegia 52,"['CPSQ6', 'spastic quadriplegic cerebral palsy 6', 'SPG52', 'autosomal recessive spastic paraplegia 52', 'AP4S1 hereditary spastic paraplegia', 'hereditary spastic paraplegia type 52', 'cerebral palsy, spastic quadriplegic, 6', 'spastic paraplegia 52, autosomal recessive', 'hereditary spastic paraplegia caused by mutation in AP4S1', 'cerebral palsy, spastic quadriplegic, 6, formerly']",0110804,614067,,C3279743,,,,,,,,
mondo:0013553,immunodeficiency-centromeric instability-facial anomalies syndrome 2,"['immunodeficiency-centromeric instability-facial anomalies syndrome type 2', 'ZBTB24 immunodeficiency-centromeric instability-facial anomalies syndrome', 'ICF syndrome 2', 'immunodeficiency-centromeric instability-facial anomalies syndrome 2', 'immunodeficiency-centromeric instability-Facial anomalies syndrome type 2', 'ICF2', 'immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in ZBTB24']",0090009,614069,,C3279748,,,,,,,,
mondo:0013554,"psoriasis 13, susceptibility to","['TRAF3IP2 psoriasis', 'psoriasis susceptibility 13', 'susceptibility to psoriasis 13', 'psoriasis caused by mutation in TRAF3IP2', 'PSORS13', 'psoriasis 13, susceptibility to']",0111287,614070,,,,,,,,,,
mondo:0013555,Hermansky-Pudlak syndrome 3,"['Hermansky-Pudlak syndrome 3', 'Hermansky-Pudlak syndrome type 3', 'Hermansky-Pudlak syndrome caused by mutation in HPS3', 'HPS3', 'HPS3 Hermansky-Pudlak syndrome']",0060541,614072,,C3888001,,,,,,,,
mondo:0013556,Hermansky-Pudlak syndrome 4,"['HPS4 Hermansky-Pudlak syndrome', 'Hermansky-Pudlak syndrome type 4', 'Hermansky-Pudlak syndrome 4', 'Hermansky-Pudlak syndrome caused by mutation in HPS4', 'HPS4']",0060542,614073,,C3484357,,,,,,,,
mondo:0013557,Hermansky-Pudlak syndrome 5,"['Hermansky-Pudlak syndrome 5', 'HPS5 Hermansky-Pudlak syndrome', 'Hermansky-Pudlak syndrome caused by mutation in HPS5', 'Hermansky-Pudlak syndrome type 5', 'HPS5']",0060543,614074,,C3888004,,,,,,,,
mondo:0013558,Hermansky-Pudlak syndrome 6,"['HPS6 Hermansky-Pudlak syndrome', 'Hermansky-Pudlak syndrome caused by mutation in HPS6', 'Hermansky-Pudlak syndrome 6', 'HPS6', 'Hermansky-Pudlak syndrome type 6']",0060544,614075,,C3888007,,C150369,,,,,,
mondo:0013559,Hermansky-Pudlak syndrome 7,"['Hermansky-Pudlak syndrome type 7', 'DTNBP1 Hermansky-Pudlak syndrome', 'HPS7', 'Hermansky-Pudlak syndrome caused by mutation in DTNBP1', 'Hermansky-Pudlak syndrome 7']",0060545,614076,231531,C3279756,"['-0.04776', '0.282', '-0.04657', '0.1566', '0.2128', '-0.2651', '-0.08075', '0.05746', '-0.206', '-0.01729', '-0.00783', '-0.0856', '-0.0683', '0.1519', '-0.009834', '-0.2302', '0.2141', '0.2157', '0.0738', '-0.3423', '0.03232', '-0.07355', '0.116', '-0.1532', '0.0799', '0.08563', '-0.0661', '0.1918', '0.11084', '0.00782', '0.2747', '0.009605', '0.2118', '-0.05927', '0.0637', '-0.04642', '-0.02167', '-0.176', '0.1084', '-0.264', '0.4106', '-0.2976', '0.0003655', '-0.1458', '-0.1906', '-0.4146', '0.05942', '0.06006', '0.2208', '-0.1209', '-0.06683', '-0.11365', '0.1528', '0.07495', '-0.1566', '-0.2764', '0.3357', '0.0783', '-0.2815', '-0.2913', '0.08185', '0.08', '0.126', '0.06216', '0.00893', '0.1813', '0.1584', '-0.10767', '-0.2472', '0.1893', '-0.2773', '-0.1295', '-0.0517', '-0.0592', '0.2323', '-0.01613', '0.00871', '-0.02472', '-0.155', '0.0443', '-0.02737', '-0.1515', '0.1344', '0.06', '-0.097', '-0.4338', '0.3105', '0.4917', '0.2673', '0.1969', '0.09143', '0.1501', '0.0754', '-0.1355', '0.5537', '0.10535', '0.0986', '-0.3044', '0.05234', '0.08594']",,,,,E70.3,,
mondo:0013560,Hermansky-Pudlak syndrome 8,"['Hermansky-Pudlak syndrome 8', 'Hermansky-Pudlak syndrome type 8', 'BLOC1S3 Hermansky-Pudlak syndrome', 'Hermansky-Pudlak syndrome caused by mutation in BLOC1S3', 'HPS8']",0060546,614077,231537,CN201510,"['-0.1318', '0.2042', '-0.0279', '0.1545', '0.3872', '-0.2656', '-0.287', '-0.004894', '-0.2124', '-0.08716', '0.0195', '-0.1603', '-0.08606', '-0.0391', '-0.067', '-0.336', '0.2008', '0.1242', '-0.08875', '-0.3538', '-0.01874', '-0.1252', '0.1761', '-0.233', '-0.0833', '-0.0164', '-0.02205', '0.1315', '0.152', '0.07477', '0.1892', '-0.06915', '0.1252', '-0.02045', '0.0318', '0.08075', '-0.01654', '-0.1691', '-0.1163', '-0.1189', '0.5366', '-0.3953', '-0.01315', '-0.2244', '-0.2225', '-0.4746', '0.1459', '0.2139', '0.3342', '-0.01151', '-0.08484', '-0.261', '0.1139', '0.078', '-0.1841', '-0.25', '0.248', '0.2313', '-0.3965', '-0.173', '-0.07056', '-0.01092', '0.273', '-0.0583', '0.1708', '0.2131', '0.3127', '-0.1207', '-0.3208', '0.3013', '-0.3232', '-0.1941', '-0.0671', '-0.1613', '0.1932', '0.1141', '0.1038', '-0.165', '-0.103', '0.09076', '0.0734', '-0.2673', '0.002659', '0.05832', '-0.0773', '-0.395', '0.3523', '0.436', '0.2317', '0.164', '0.181', '0.00962', '0.08014', '-0.2484', '0.636', '0.2664', '0.1528', '-0.3452', '-0.07367', '0.0638']",,,,,E70.3,,
mondo:0013561,"chondrodysplasia with joint dislocations, gPAPP type","['gPAPP deficiency', 'chondrodysplasia with joint dislocations, gPAPP type']",0112224,614078,280586,C3279757,"['0.1863', '-0.342', '-0.4434', '0.154', '-0.08374', '-0.3943', '-0.08307', '0.5986', '-0.9893', '-0.8306', '0.261', '0.752', '0.3962', '0.727', '-0.00914', '0.0923', '0.074', '-0.367', '-0.9307', '-0.1407', '0.8545', '0.695', '0.0593', '0.3018', '-0.3013', '0.2998', '-0.685', '-0.1145', '0.1247', '-0.52', '0.00776', '-0.3843', '-0.1366', '-0.1835', '0.6543', '0.1931', '0.2251', '-0.6846', '0.3406', '-0.822', '0.0705', '0.01909', '-0.4385', '0.9478', '-0.4014', '-0.2537', '-0.442', '0.401', '0.7817', '-0.3076', '-0.02731', '-0.5117', '0.722', '0.2747', '-0.3484', '-0.6606', '-0.6816', '-0.421', '-0.2236', '-0.005844', '-0.06274', '0.2595', '-0.7036', '0.2617', '-0.2188', '0.3032', '-0.203', '0.96', '-0.03638', '0.3188', '-0.2223', '-0.008286', '0.2201', '-0.937', '0.269', '-0.0931', '0.03333', '0.642', '-0.1316', '-0.0847', '-0.475', '0.3691', '-0.587', '1.282', '-0.204', '0.10394', '0.3782', '0.647', '0.7705', '-0.08484', '0.1162', '0.4255', '-0.6943', '0.316', '0.2136', '0.1385', '0.54', '-0.5513', '0.7764', '-0.1604']",,,,,,,
mondo:0013562,"aspergillosis, susceptibility to","['aspergillosis, susceptibility to', 'susceptibility to aspergillosis']",,614079,,,"['-0.044', '0.03137', '0.01859', '-0.0475', '0.03113', '-0.1019', '0.03546', '0.03726', '-0.03616', '-0.0584', '-0.0131', '0.02168', '-0.03111', '0.02832', '-0.0341', '-0.05692', '0.0245', '-0.0606', '-0.046', '-0.1322', '0.04016', '-0.03934', '0.08826', '0.003004', '-0.02666', '-0.03467', '-0.03146', '-0.002398', '-0.01418', '-0.05292', '0.05115', '-0.03696', '0.0889', '0.01875', '0.04376', '-0.05038', '-0.0584', '-0.01451', '-0.0308', '-0.07', '0.02777', '-0.006798', '0.02426', '-0.039', '-0.00971', '-0.1013', '0.001488', '0.04825', '0.02092', '0.02005', '-0.02296', '-0.0157', '0.06204', '-0.006252', '-0.007294', '-0.002317', '0.03168', '-0.03604', '-0.06915', '0.00561', '0.01107', '0.05087', '-0.007965', '0.02374', '0.02965', '0.03644', '0.05145', '0.0991', '-0.0921', '0.11743', '-0.02843', '0.0008545', '0.01646', '-0.08527', '0.012794', '0.04822', '-0.00495', '0.000812', '0.003063', '-0.0157', '-0.02687', '-0.005226', '0.002768', '0.1049', '-0.0406', '-0.002481', '0.026', '0.06494', '0.09827', '-0.011375', '0.03262', '0.0755', '-0.02118', '0.02754', '0.1407', '0.07825', '0.0641', '-0.0674', '-0.01674', '0.01633']",,,,,,,
mondo:0013563,multiple congenital anomalies-hypotonia-seizures syndrome 1,"['multiple congenital anomalies-hypotonia-seizures syndrome', 'multiple congenital anomalies - hypotonia - seizures syndrome', 'glycosylphosphatidylinositol biosynthesis defect 3', 'MCAHS1', 'multiple congenital anomalies-hypotonia-seizures syndrome 1', 'multiple congenital anomalies/dysmorphic syndrome-intellectual disability caused by mutation in PIGN', 'inherited GPI anchor-deficiency', 'multiple congenital anomalies-hypotonia-seizures syndrome type 1', 'PIGN multiple congenital anomalies/dysmorphic syndrome-intellectual disability', 'PIGN-CDG', 'PIGN-related inherited GPI deficiency', 'congenital disorder of glycosylation due to PIGN deficiency']",0080138,614080,280633,C3279775,"['0.05182', '-0.04034', '0.10614', '0.1378', '-0.361', '-0.1744', '0.8228', '0.4272', '-0.3264', '-0.11487', '-0.1908', '-0.3936', '0.0808', '0.4275', '-0.912', '0.2024', '-0.09863', '-0.1223', '0.00843', '-0.3967', '0.1792', '1.064', '0.0342', '-0.1793', '-0.06964', '-0.2815', '-0.1262', '0.1389', '0.1514', '0.4143', '0.1931', '-0.04507', '0.253', '0.1378', '0.662', '0.2301', '-0.1718', '-0.471', '-0.0384', '-0.5483', '-0.1743', '-0.03079', '-0.2255', '-0.2942', '0.1043', '-0.2052', '0.1906', '0.8374', '0.1431', '0.77', '-0.3564', '0.206', '0.1594', '-0.727', '-0.311', '-0.02794', '-0.1991', '0.3108', '-0.2416', '-0.03857', '-0.0931', '0.62', '0.1741', '0.04468', '-0.521', '0.9985', '0.2932', '-0.12427', '-0.685', '0.776', '0.1614', '0.617', '0.0942', '-0.2769', '0.092', '0.4739', '0.905', '0.2195', '-0.2366', '0.03882', '0.1359', '0.831', '0.4358', '0.1215', '0.10913', '0.0953', '-0.11334', '0.846', '0.2234', '1.068', '0.0588', '0.4553', '0.475', '0.0862', '0.1527', '-0.0738', '0.1538', '-0.2524', '0.3525', '0.553']",C176896,,,,,,
mondo:0013564,anhaptoglobinemia,"['AHP', 'ANHAPTOGLOBINEMIA', 'anhaptoglobinemia', 'hypohaptoglobinemia', 'Ahaptoglobinemia']",,614081,,C3279786,"['-0.00133', '0.00737', '-0.00592', '0.009476', '0.002499', '-0.002356', '0.00664', '0.00863', '0.002872', '0.004642', '-0.00767', '-0.000822', '0.001849', '0.013466', '-0.009285', '-0.001343', '0.01002', '-0.007015', '-0.005417', '-0.01342', '0.00497', '-0.003561', '0.0007157', '-0.00785', '-0.0003693', '0.002037', '0.006645', '0.006256', '-0.007473', '0.002287', '-0.001591', '-7.71e-05', '0.00827', '0.002932', '0.002607', '-0.001639', '-0.00946', '0.007767', '0.00848', '-0.002016', '0.003542', '0.004448', '0.000252', '0.004604', '-0.003378', '-0.01204', '-0.00676', '0.00921', '0.00029', '-0.00705', '0.007587', '0.0016', '0.0008388', '0.0008407', '0.003052', '0.005985', '-0.00125', '-0.006374', '-0.00505', '-0.002892', '0.000882', '-0.003893', '-0.007935', '-0.002253', '-0.00919', '0.00455', '0.00455', '0.01007', '0.0001771', '0.007587', '-0.0091', '-0.00516', '-0.00104', '-0.000522', '-0.001813', '-0.00595', '0.00697', '0.0006995', '0.00422', '-0.003345', '0.006268', '-0.00652', '0.004173', '-0.004814', '-0.001773', '0.001687', '-0.007317', '2.58e-05', '0.006935', '0.004063', '0.00167', '0.001701', '0.005424', '-0.00741', '0.008064', '-0.004772', '0.01006', '0.000867', '0.005737', '-0.00917']",,,,,,,
mondo:0013565,Fanconi anemia complementation group G,"['Fanconi anemia, complementation group G', 'Fanconi Anemia, complementation group type G', 'Fanconi anemia complementation group type G', 'Fanconi anaemia complementation group type G', 'FANCG']",0111086,614082,,,"['-0.3225', '0.4072', '-0.0839', '0.1989', '0.6494', '0.1588', '-0.3596', '0.581', '-0.1943', '-0.5024', '0.834', '0.03726', '0.2122', '0.6274', '-1.032', '0.1427', '-0.539', '0.187', '-0.4578', '-0.3323', '-0.1589', '-0.6665', '0.5557', '-0.2477', '0.9263', '-0.4636', '-0.203', '-0.2355', '0.6567', '0.08167', '0.2294', '0.0881', '0.4011', '0.61', '0.5464', '-0.2622', '-0.8022', '-0.565', '0.576', '-0.2686', '-0.696', '0.1902', '0.0759', '-0.587', '-0.611', '-0.9707', '0.3037', '0.1482', '0.425', '-0.1967', '0.621', '0.3638', '0.8354', '-0.1254', '0.4927', '-0.761', '0.1709', '0.5396', '-1.095', '0.1665', '0.04315', '0.2996', '-0.3691', '-0.4048', '-0.2424', '0.4111', '0.3088', '0.695', '-0.686', '1.105', '0.7905', '-0.3909', '-0.5444', '-0.6143', '0.2886', '0.978', '0.2544', '0.3965', '0.01046', '0.2957', '0.2603', '-0.3105', '0.0713', '0.05304', '0.596', '-0.5205', '-0.7075', '0.338', '0.9106', '-0.3274', '0.551', '0.2869', '-0.225', '-0.05087', '0.548', '1.052', '0.2164', '-0.1208', '0.3323', '-0.4795']",C125708,0009046,,,,,
mondo:0013566,Fanconi anemia complementation group L,"['FANCL', 'Fanconi Anemia, complementation group type 50', 'FANCL Fanconi anaemia', 'FANCL Fanconi anemia', 'Fanconi anaemia complementation group type L', 'Fanconi anemia caused by mutation in FANCL', 'Fanconi anemia complementation group type L', 'Fanconi anemia, complementation group L', 'Fanconi Anemia, complementation Group 50', 'Fanconi anaemia caused by mutation in FANCL']",0111082,614083,,,,,,,,,,
mondo:0013567,atrial septal defect 3,"['atrial heart septal defect caused by mutation in MYH6', 'atrial heart septal defect type 3', 'atrial septal defect 3', 'atrial septal defect type 3', 'MYH6 atrial heart septal defect', 'ASD3']",0110108,614089,,C3279790,,,,C563540,,,,
mondo:0013568,"sick sinus syndrome 3, susceptibility to","['sick sinus syndrome 3', 'MYH6 familial sick sinus syndrome', 'familial sick sinus syndrome caused by mutation in MYH6', 'sick sinus syndrome 3, susceptibility to', 'susceptibility to sick sinus syndrome 3', 'SSS3']",,614090,,,,,,,,,,
mondo:0013569,short-rib thoracic dysplasia 7 with or without polydactyly,"['short rib-polydactyly syndrom type V', 'short-rib thoracic dysplasia 7 with or without polydactyly', 'short rib-polydactyly syndrome, type 5', 'SRTD7', 'SRPS5', 'short rib-polydactyly syndrome type 5']",0110090,614091,498497,C3279792,,,,,,,,
mondo:0013570,combined oxidative phosphorylation defect type 8,"['combined oxidative phosphorylation deficiency 8', 'cardiomyopathy, hypertrophic mitochondrial, fatal infantile', 'combined oxidative phosphorylation deficiency caused by mutation in AARS2', 'combined oxidative phosphorylation deficiency type 8', 'COXPD8', 'AARS2 combined oxidative phosphorylation deficiency']",0111479,614096,319504,C4518839,"['-0.712', '0.1896', '0.094', '-0.1757', '0.322', '-0.4653', '0.253', '0.3513', '-0.51', '0.11334', '-0.3787', '-0.2404', '0.1026', '-0.3403', '-0.0939', '-0.3027', '-0.12054', '-0.225', '-0.5967', '-0.6675', '0.4382', '-0.3506', '0.767', '0.1998', '-0.057', '-0.134', '0.1852', '0.437', '-0.1545', '-0.2389', '0.261', '0.4753', '0.829', '-0.181', '0.05435', '-0.885', '0.11285', '-0.0925', '0.0268', '-0.3035', '-0.2185', '-0.3796', '0.0469', '0.6616', '-0.5415', '0.05457', '0.05264', '0.3545', '0.05103', '-0.0298', '-0.3638', '-0.2021', '0.2725', '0.1769', '-0.3806', '-0.551', '0.2837', '0.214', '-0.02455', '0.4053', '-0.05066', '0.1152', '0.446', '0.1592', '-0.656', '0.09814', '0.1508', '0.2118', '-0.7324', '0.02892', '-0.3252', '-0.11084', '0.2451', '0.0984', '0.05853', '-0.04797', '0.3127', '-0.1501', '-0.014755', '0.4841', '0.2346', '-0.1357', '0.08966', '0.03195', '-0.106', '-0.1771', '0.5312', '0.9033', '0.524', '-0.10065', '0.04636', '-0.09143', '0.11664', '-0.1918', '0.7134', '0.4844', '0.5327', '-0.2355', '0.03662', '-0.03117']",,,,,,,
mondo:0013571,acatalasia,"['catalase deficiency', 'acatalasia', 'deficiency of catalase', 'acatalasemia']",2582,614097,926,C0268419,"['-0.4314', '0.1417', '-0.307', '-0.1696', '0.3555', '-0.1296', '0.2576', '-0.07275', '0.09424', '-0.324', '-0.03488', '0.1248', '0.221', '0.02043', '-0.4556', '-0.3113', '0.258', '-0.002747', '-0.4875', '-0.6343', '0.06198', '-0.5903', '0.416', '-0.1871', '-0.3481', '-0.1041', '-0.014244', '-0.1217', '0.122', '-0.5015', '0.3206', '0.3816', '-0.2361', '0.312', '-0.1819', '0.10504', '0.1768', '-0.5225', '0.0903', '-0.1005', '-0.10236', '-0.1383', '0.07166', '0.0395', '-0.5464', '-0.364', '0.5425', '-0.0805', '0.4504', '0.06946', '0.4094', '-0.04904', '0.3682', '-0.3335', '0.0552', '-0.262', '0.621', '-0.2267', '-0.7583', '0.00646', '0.02937', '0.2979', '0.558', '-0.2722', '0.01491', '0.1631', '0.10974', '0.2036', '-0.655', '0.2208', '-0.4126', '-0.324', '-0.2203', '0.1605', '0.419', '0.329', '0.243', '0.3286', '0.012566', '-0.222', '-0.5264', '-0.295', '0.269', '0.7056', '-0.1915', '-0.00541', '0.0664', '0.03888', '0.2913', '-0.2225', '0.43', '0.1824', '0.0958', '-0.2808', '0.6025', '0.3892', '0.4893', '-0.581', '-0.2241', '-0.1627']",C84526,0004144,D020642,277.6,,,
mondo:0013572,Keppen-Lubinsky syndrome,"['Keppen-Lubinsky syndrome', 'generalised lipodystrophy-progeroid features-severe intellectual disability syndrome', 'KPLBS', 'KEPPEN-Lubinsky syndrome', 'generalized lipodystrophy-progeroid features-severe intellectual disability syndrome']",,614098,435628,C3279800,"['0.002129', '0.01237', '-0.003496', '0.002844', '0.013466', '-0.01675', '0.003132', '0.01947', '-0.00723', '-0.009254', '-0.01215', '0.000613', '0.00972', '0.01029', '0.003157', '-0.004772', '0.00352', '-0.002459', '-0.02063', '-0.02559', '-0.006268', '-0.01241', '0.01706', '-0.014015', '0.0111', '0.002941', '-0.006664', '-0.004585', '0.002062', '-0.012794', '0.01021', '0.003515', '0.0282', '0.01645', '-0.005264', '-0.002941', '-0.000802', '-0.006947', '0.003914', '-0.01726', '0.00589', '-0.01227', '0.00614', '-0.019', '0.01268', '-0.0189', '-0.0006943', '0.02126', '0.00947', '-0.005566', '-0.01712', '-0.007442', '0.001926', '-0.00542', '-0.01343', '-0.00372', '0.02042', '-0.00694', '-0.01898', '-0.004276', '0.01289', '0.007557', '0.010345', '0.0106', '-0.00501', '-0.00821', '0.02022', '0.007595', '-0.00821', '0.03207', '-0.02432', '0.01073', '0.006264', '-0.0141', '0.01273', '0.010574', '0.00536', '-0.004597', '-0.009254', '-0.01118', '0.01441', '-0.00593', '-0.01182', '0.01695', '-0.0010605', '0.007233', '-0.001616', '0.01892', '0.01772', '0.00548', '0.01701', '0.02553', '0.007744', '-0.004272', '0.03772', '0.01288', '0.02725', '-0.03452', '0.0007434', '0.00779']",,,,,,,
mondo:0013573,cranioectodermal dysplasia 3,"['CED3', 'CRANIOECTODERMAL dysplasia 3', 'Cranioectodermal dysplasia type 3', 'cranioectodermal dysplasia 3', 'cranioectodermal dysplasia caused by mutation in IFT43', 'IFT43 cranioectodermal dysplasia']",0080805,614099,,C3279807,,,,,,,,
mondo:0013574,cutis laxa - Marfanoid syndrome,"['cutis laxa - Marfanoid syndrome', 'cutis laxa, neonatal, with MARFANOID phenotype']",,614100,171719,C0432335,,,,C563639,,,,
mondo:0013575,plasma fibronectin deficiency,['plasma fibronectin deficiency'],,614101,,,,,,,,,,
mondo:0013576,recurrent infections associated with rare immunoglobulin isotypes deficiency,"['isolated IgG subclass deficiency', 'IMMUNOGLOBULIN kappa LIGHT chain deficiency', 'IgG subclass deficiency with IgA subclass deficiency', 'selective IgG subclass deficiency', 'IGKCD', 'kappa light chain deficiency', 'kappa chain deficiency', 'kappa-chain deficiency']",,614102,183675,C3279824,"['0.4497', '0.2903', '-0.3462', '-0.264', '-0.3618', '-0.2524', '0.559', '-0.02597', '-0.1371', '-0.2281', '-0.04', '0.3813', '-0.5156', '0.4421', '-0.1874', '-0.3818', '0.0499', '-0.4888', '-0.543', '-0.372', '-0.4495', '-0.2174', '0.7666', '-0.0754', '0.574', '0.0842', '-0.414', '-0.01608', '-0.3486', '-0.205', '0.2394', '0.2637', '0.0004992', '0.3687', '-0.01419', '-0.301', '-0.189', '-0.389', '-0.4604', '0.2213', '0.1526', '0.0776', '0.3752', '-0.07404', '-0.3547', '-0.069', '-0.3992', '-0.4048', '-0.287', '1.098', '-0.1593', '-0.2318', '0.1992', '-0.2588', '-0.307', '0.4946', '0.2568', '-0.3862', '-0.0863', '0.3313', '0.132', '0.804', '-0.12036', '-0.2332', '0.3853', '-0.04745', '0.3096', '0.4111', '0.05032', '0.3215', '-0.02483', '-0.06274', '-0.4111', '-0.764', '0.4128', '-0.1627', '0.5156', '-0.3003', '0.0395', '0.3574', '-0.09467', '-0.07654', '-0.1464', '0.07336', '-0.3047', '0.0708', '0.1033', '0.3325', '0.3774', '0.1774', '0.1809', '0.4773', '-0.2253', '-0.2559', '0.6777', '0.9595', '-0.1664', '-0.7534', '-0.4233', '0.1885']",,,C564131,,,,
mondo:0013577,Lipedema,"['Lipedema (disease)', 'lipedema']",,614103,77243,C0020473,,,,D065134,,,10063955,0100695
mondo:0013578,DYRK1A-related intellectual disability syndrome,"['autosomal dominant intellectual disability 7', 'mental retardation, autosomal dominant type 7', 'autosomal dominant non-syndromic intellectual disability 7', 'mental retardation, autosomal dominant 7', 'autosomal dominant mental retardation 7', 'intellectual disability, autosomal dominant type 7', 'intellectual disability, autosomal dominant 7', 'MRD7']",0070037,614104,464306,C3279839,"['-0.03069', '0.06726', '0.03072', '-0.04993', '0.0411', '-0.1044', '0.01796', '0.1064', '-0.07526', '-0.0848', '-0.0266', '-0.009155', '0.01262', '0.01047', '-0.007484', '-0.03836', '-0.00916', '-0.01685', '-0.0599', '-0.1508', '0.00888', '0.010864', '0.03128', '-0.02734', '0.05005', '-0.0311', '-0.015205', '0.0003598', '0.02269', '-0.03934', '0.0808', '-0.03384', '0.1072', '0.04532', '0.03108', '-0.05682', '-0.01825', '-0.08185', '-0.02773', '-0.0723', '0.07074', '-0.0799', '0.01368', '-0.02222', '-0.01002', '-0.0784', '-0.0363', '0.05655', '-0.005688', '-0.01233', '-0.0368', '0.01947', '0.005226', '-0.02254', '-0.02681', '-0.01142', '0.05154', '-0.01646', '-0.07135', '0.03436', '0.04224', '0.00768', '0.01045', '0.02669', '-0.01274', '0.02583', '0.04803', '0.0807', '-0.06537', '0.07227', '-0.094', '0.00791', '0.0241', '-0.05954', '0.0457', '0.0459', '0.04916', '-0.01353', '-0.04404', '-0.03503', '-0.03378', '0.01129', '-0.05524', '0.1002', '0.006237', '0.01877', '0.02489', '0.095', '0.1016', '0.0651', '0.02264', '0.0985', '0.002586', '0.01878', '0.151', '0.0326', '0.0682', '-0.11035', '0.04956', '0.05988']",,,,,,,
mondo:0013579,methylmalonate semialdehyde dehydrogenase deficiency,"['methylmalonate semialdehyde dehydrogenase deficiency', 'MMSDHD', 'developmental delay due to MMSDH deficiency', 'developmental delay due to ALDH6A1 deficiency', 'MMSDH deficiency', 'developmental delay due to methylmalonate semialdehyde dehydrogenase deficiency']",,614105,289307,C3279840,"['-0.6416', '0.1323', '0.1348', '-0.1968', '0.1583', '-0.08734', '-0.3486', '0.341', '-0.2854', '0.1637', '-0.3618', '-0.248', '0.1923', '-0.2646', '-0.346', '-0.10767', '0.10034', '-0.2274', '-0.5234', '-0.695', '0.263', '-0.2537', '0.4731', '-0.1407', '-0.1971', '-0.2708', '-0.00896', '0.003086', '-0.10187', '-0.1984', '0.1759', '0.07904', '0.604', '0.3008', '-0.1731', '-0.2015', '-0.3738', '-0.1199', '-0.2932', '-0.1433', '0.1963', '-0.3896', '0.1561', '-0.1587', '-0.5615', '-0.4172', '0.3499', '0.02666', '-0.2932', '0.3', '-0.3167', '0.02094', '-0.1798', '-0.2583', '-0.3284', '0.1351', '0.25', '-0.1527', '-0.366', '0.4392', '0.2356', '-0.0376', '0.1993', '-0.2323', '-0.01767', '-0.05292', '0.5293', '0.3328', '-0.4', '0.0517', '-0.2017', '0.2903', '-0.2043', '0.076', '-0.2454', '0.09204', '0.4238', '-0.4182', '0.01714', '-0.0131', '0.3196', '-0.03683', '-0.05075', '0.4329', '0.2864', '0.3252', '-0.152', '0.1533', '0.4165', '0.3489', '0.568', '0.2134', '-0.139', '-0.11566', '0.467', '0.518', '0.3218', '-0.1965', '0.2018', '0.0962']",,,C566402,,,,
mondo:0013580,pyruvate dehydrogenase E1-beta deficiency,"['PDHBD', 'pyruvate dehydrogenase E1-BETA deficiency', 'pyruvate dehydrogenase complex E1 component subunit beta deficiency', 'pyruvate dehydrogenase E1-beta deficiency']",,614111,255138,C3279841,"['-0.3984', '0.3403', '-0.11145', '0.1583', '0.1004', '-0.411', '-0.2573', '0.562', '0.083', '-0.1481', '-0.1273', '-0.1458', '-0.1104', '-0.2351', '0.07837', '0.236', '0.09015', '-0.2568', '-0.5474', '-0.773', '-0.2352', '0.00921', '0.817', '-0.2198', '0.0982', '-0.1103', '-0.285', '0.02327', '0.2057', '-0.202', '0.1409', '0.2445', '0.2487', '0.368', '-0.2083', '-0.2288', '-0.2825', '-0.2917', '-0.246', '0.1095', '0.1714', '-0.625', '-0.1305', '-0.2424', '-0.1826', '-0.10675', '0.0897', '0.2886', '0.1181', '0.3337', '-0.2377', '-0.3442', '-0.1548', '-0.05515', '-0.0555', '-0.2246', '0.3408', '-0.3235', '-0.05075', '0.5347', '0.2078', '-0.353', '0.6465', '-0.000715', '0.07477', '0.1461', '0.263', '0.4998', '-0.764', '0.4202', '0.1476', '0.09143', '-0.1398', '-0.05038', '0.0869', '0.493', '0.4082', '-0.348', '-0.2864', '0.4229', '0.52', '0.0304', '-0.2693', '0.02293', '0.563', '0.314', '0.11304', '0.10175', '0.851', '0.07574', '0.579', '0.419', '-0.2917', '-0.07184', '0.638', '0.652', '0.0897', '-0.3267', '0.298', '-0.1969']",,,C566729,,,,
mondo:0013581,"intellectual disability, autosomal dominant 2","['mental retardation, autosomal dominant type 2', 'autosomal dominant intellectual disability 2', 'autosomal dominant non-syndromic intellectual disability caused by mutation in DOCK8', 'MRD2', 'intellectual disability, autosomal dominant type 2', 'mental retardation, autosomal dominant 2', 'autosomal dominant non-syndromic intellectual disability 2', 'intellectual disability, autosomal dominant 2', 'DOCK8 autosomal dominant non-syndromic intellectual disability', 'autosomal dominant mental retardation 2']",0070032,614113,,C3279842,,,,,,,,
mondo:0013582,mosaic variegated aneuploidy syndrome 2,"['mosaic variegated aneuploidy syndrome type 2', 'MVA2', 'mosaic variegated aneuploidy syndrome 2', 'MOSAIC variegated aneuploidy syndrome 2', 'Mosaic variegated aneuploidy syndrome type 2', 'CEP57 mosaic variegated aneuploidy syndrome', 'mosaic variegated aneuploidy syndrome caused by mutation in CEP57']",0080142,614114,,C3279843,,C168989,,,,,,
mondo:0013583,occipital pachygyria and polymicrogyria,"['occipital malformations of cortical development', 'OCCM', 'cortical malformations, occipital', 'occipital MCD']",,614115,280640,C3279875,"['-0.2551', '0.10114', '0.2693', '-0.4722', '-0.0845', '0.1063', '0.226', '0.253', '-0.2732', '0.0967', '-0.3562', '-0.3958', '-0.09753', '-0.4307', '-0.11456', '-0.03995', '0.2727', '-0.1819', '-0.1715', '-0.5825', '-0.0872', '0.11945', '0.3315', '-0.1615', '0.338', '-0.2024', '-0.102', '-0.1838', '-0.1962', '0.2289', '0.2294', '-0.1644', '0.3613', '0.2354', '0.1515', '0.1708', '-0.1521', '-0.1123', '-0.1947', '-0.4077', '0.3716', '-0.4514', '-0.05566', '-0.2563', '-0.073', '-0.307', '-0.1852', '0.1078', '0.0753', '0.2285', '0.1549', '0.3325', '-0.04166', '-0.07495', '-0.2922', '0.2017', '0.02466', '-0.1892', '-0.3882', '0.10547', '-0.1792', '-0.06134', '0.02708', '-0.1918', '-0.346', '0.07263', '0.4292', '0.274', '-0.3625', '0.4043', '-0.07263', '0.3506', '0.2467', '-0.12305', '-0.1233', '-0.12476', '0.4373', '-0.1586', '-0.2532', '-0.0848', '0.052', '0.10846', '0.1752', '0.2208', '-0.014465', '-0.3884', '-0.09125', '0.3748', '0.2876', '0.00632', '0.0773', '0.435', '-0.025', '0.0715', '0.2734', '0.05518', '0.366', '-0.2524', '0.2832', '0.4414']",,,,,,,
mondo:0013584,hereditary sensory neuropathy-deafness-dementia syndrome,"['neuropathy, hereditary sensory, type IE', 'hereditary sensory and autonomic neuropathy type 1E', 'hereditary sensory neuropathy type IE', 'DNMT1-related dementia, deafness, and sensory neuropathy', 'HSN1E', 'hereditary sensory neuropathy with hearing loss and dementia', 'hereditary sensory neuropathy-sensorineural hearing loss-dementia syndrome', 'HSAN1E', 'neuropathy, hereditary sensory, type 1E', 'HSNIE', 'neuropathy, hereditary sensory, with hearing loss and dementia', 'hereditary sensory neuropathy type 1E', 'HSN 1E']",0070158,614116,456318,C3279885,,,,C580162,,,,
mondo:0013585,hydrolethalus syndrome 2,"['HLS2', 'hydrolethalus syndrome type 2', 'hydrolethalus syndrome 2', 'KIF7 hydrolethalus syndrome', 'hydrolethalus syndrome caused by mutation in KIF7']",0111356,614120,,C3279899,,,,,,,,
mondo:0013587,glycogen storage disease due to lactate dehydrogenase H-subunit deficiency,"['lactate dehydrogenase-B deficiency', 'lactate dehydrogenase B deficiency', 'LDH deficiency B', 'LDHBD', 'lactate dehydrogenase deficiency type B', 'LDH-H subunit deficiency', 'GSD due to lactate dehydrogenase H-subunit deficiency', 'glycogenosis due to lactate dehydrogenase H-subunit deficiency']",,614128,284435,C3279904,"['0.0982', '0.3958', '-0.4246', '0.2847', '0.012825', '-0.283', '-0.1332', '0.3875', '-0.318', '-0.2595', '0.3076', '-0.0635', '-0.012505', '-0.005802', '-0.2844', '0.1805', '-0.4314', '-0.02794', '-0.834', '-0.1808', '0.281', '-0.2101', '0.267', '0.2249', '0.02922', '-0.1279', '0.1453', '-0.1128', '-0.1404', '0.566', '0.3564', '-0.0616', '0.2876', '-0.0942', '0.1727', '-0.1362', '-0.06555', '0.03986', '0.3025', '-0.2603', '-0.0706', '-0.335', '-0.1516', '0.4888', '-0.2451', '-0.2786', '0.312', '0.1323', '-0.007126', '0.1855', '-0.02397', '-0.11676', '0.2383', '-0.2219', '0.1764', '-0.2246', '0.02106', '0.1736', '-0.4075', '0.05203', '0.5156', '-0.0964', '0.6377', '0.0821', '-0.4878', '0.3066', '0.03323', '0.04004', '-0.4604', '0.2196', '-0.3367', '0.00345', '-0.01884', '0.2164', '0.269', '0.226', '0.259', '0.431', '-0.2179', '0.01736', '-0.02774', '-0.1099', '-0.01833', '-0.2935', '-0.03854', '0.3247', '-0.02464', '-0.1755', '0.844', '0.2131', '0.6885', '0.04187', '-0.131', '-0.1071', '0.78', '0.751', '-0.1239', '-0.377', '-0.2087', '0.2351']",,,C563641,,,,
mondo:0013588,Perrault syndrome 3,"['deafness, autosomal recessive 81, formerly', 'Perrault syndrome type 3', 'CLPP Perrault syndrome', 'deafness, autosomal recessive 81', 'Perrault syndrome caused by mutation in CLPP', 'PRLTS3', 'Perrault syndrome 3']",,614129,,C3808414,,,,,,,,
mondo:0013589,focal segmental glomerulosclerosis 6,"['MYO1E focal segmental glomerulosclerosis', 'focal segmental glomerulosclerosis type 6', 'focal segmental glomerulosclerosis caused by mutation in MYO1E', 'FSGS6', 'glomerulosclerosis, focal segmental, 6', 'focal segmental glomerulosclerosis 6']",0111131,614131,656,C3279905,,,,,,,,
mondo:0013590,"Stickler syndrome, type 4","['STL4', 'COL9A1 autosomal recessive Stickler syndrome', 'STICKLER syndrome, type IV', 'autosomal recessive Stickler syndrome caused by mutation in COL9A1']",,614134,,,,,,,,,,
mondo:0013591,"epiphyseal dysplasia, multiple, 6","['epiphyseal dysplasia, multiple, type 6', 'EDM6', 'COL9A1 multiple epiphyseal dysplasia (disease)', 'multiple epiphyseal dysplasia 6', 'epiphyseal dysplasia, multiple, 6']",0070301,614135,,C2675767,,,,,,,,
mondo:0013592,nonsyndromic congenital nail disorder 9,"['nail disorder, nonsyndromic congenital, 9', 'anonychia-onycholysis, isolated', 'nonsyndromic congenital nail disorder type 9', 'nail dysplasia', 'onychodystrophy', 'NDNC9']",0080087,614149,,C3279947,,,,,703.8,,,
mondo:0013593,autosomal dominant nonsyndromic hearing loss 64,"['deafness, autosomal dominant 64', 'autosomal dominant deafness 64', 'autosomal dominant nonsyndromic deafness 64', 'deafness, autosomal dominant type 64', 'autosomal dominant nonsyndromic deafness type 64', 'DFNA64', 'autosomal dominant nonsyndromic deafness caused by mutation in DIABLO', 'DIABLO autosomal dominant nonsyndromic deafness']",0110585,614152,,C3279948,,,,,,,,
mondo:0013594,spinocerebellar ataxia type 36,"['spinocerebellar ataxia 36', 'SCA36', 'Asidan', 'spinocerebellar ataxia type 36']",0050983,614153,276198,C3472711,"['-0.0885', '-0.1543', '-0.196', '0.0712', '-0.3076', '-0.7866', '0.4185', '0.532', '-0.538', '-1.011', '0.2534', '0.09973', '-0.1135', '0.0945', '0.6235', '-0.3096', '-0.216', '-0.4526', '0.2246', '-0.8145', '-0.1387', '-0.4653', '0.2416', '-0.5312', '0.1289', '-0.5405', '-0.394', '0.252', '-0.0257', '-0.76', '0.2788', '0.2886', '-0.6724', '-0.4463', '0.208', '0.04672', '-0.1068', '0.08185', '0.3691', '0.6445', '0.4175', '0.02834', '-0.605', '0.3015', '0.4468', '-0.4756', '-0.010216', '0.5396', '0.302', '-0.08984', '-0.3213', '0.1322', '0.058', '-0.5586', '0.01532', '-0.6353', '0.4949', '0.4614', '-0.005093', '0.3533', '-0.6104', '0.3584', '0.209', '-0.1847', '-0.4417', '0.571', '0.283', '0.2385', '-0.503', '0.2668', '0.549', '0.342', '-0.2966', '-0.721', '0.9185', '0.3362', '0.2915', '0.10095', '0.0658', '0.4602', '-0.1619', '-1.001', '0.4226', '0.783', '-0.2246', '-0.496', '0.1794', '0.02325', '0.449', '0.2905', '0.4124', '0.2003', '-0.07074', '-0.2349', '1.031', '0.823', '0.34', '0.4666', '-0.11676', '-0.1211']",C148316,,,,,,
mondo:0013595,hyperbiliverdinemia,"['hyperbiliverdinemia', 'HBLVD', 'green jaundice']",,614156,276405,C3279964,"['-0.2059', '-0.1183', '0.1812', '-0.4094', '0.3733', '-0.102', '-0.557', '-0.0901', '0.03137', '-0.1501', '-0.194', '-0.3108', '0.1565', '-0.1311', '-0.596', '-0.2101', '0.09546', '-0.2017', '-0.4873', '-0.8716', '0.001081', '-0.292', '0.1941', '0.1126', '0.1254', '-0.003986', '-0.1051', '0.4639', '0.2166', '-0.2566', '0.7266', '-0.192', '0.1682', '-0.2576', '-0.02945', '-0.3145', '-0.503', '-0.2478', '0.1243', '-0.2253', '-0.4275', '-0.10187', '0.2544', '-0.339', '-0.218', '-0.01923', '0.6045', '-0.0609', '-0.0449', '0.1271', '-0.3667', '0.09424', '0.678', '-0.2314', '-0.4565', '-0.04892', '0.2122', '-0.0003707', '-0.688', '0.04343', '0.4478', '0.3313', '-0.02126', '-0.642', '0.435', '-0.2068', '0.234', '0.2468', '-0.664', '-0.0327', '-0.4685', '0.342', '-0.1357', '-0.2305', '-0.04388', '0.1986', '0.326', '0.1521', '0.1246', '0.2715', '-0.1378', '-0.002565', '0.355', '0.2585', '-0.01079', '-0.238', '-0.0974', '0.1221', '0.2598', '0.1069', '0.1696', '0.1324', '-0.04932', '-0.2603', '0.5366', '0.2181', '0.1367', '-0.4229', '-0.1393', '0.2007']",,,,,,,
mondo:0013597,platelet-type bleeding disorder 14,"['bleeding disorder, platelet-type, 14', 'inherited bleeding disorder, platelet-type caused by mutation in TBXAS1', 'TBXAS1 inherited bleeding disorder, platelet-type', 'BDPLT14', 'thromboxane synthetase deficiency', 'thromboxane synthase deficiency']",0111047,614158,,C0398635,,,,C562866,,,,
mondo:0013598,myostatin-related muscle hypertrophy,"['muscle hypertrophy', 'MSLHP']",0111072,614160,275534,,"['-0.2056', '0.269', '-0.2551', '-0.04846', '0.1608', '-0.2028', '-0.07904', '0.4626', '-0.263', '-0.3782', '0.04156', '0.0321', '-0.1677', '0.0928', '0.1458', '0.1289', '-0.1448', '0.167', '-0.3337', '-0.604', '0.2083', '-0.03766', '0.2256', '0.2502', '0.1394', '0.008766', '0.03146', '-0.2499', '-0.1993', '0.1315', '0.4922', '-0.2903', '0.1674', '-0.0207', '-0.03296', '0.02954', '-0.02232', '-0.05164', '0.4663', '-0.4246', '0.1242', '-0.2947', '-0.1475', '0.07336', '0.013084', '-0.1561', '0.03143', '0.01001', '0.1716', '0.0529', '0.06226', '-0.278', '0.1858', '-0.1298', '-0.1315', '-0.2404', '0.2339', '0.1565', '0.0635', '-0.1449', '0.184', '0.2443', '-0.01163', '-0.2057', '-0.3308', '0.2157', '0.09576', '0.2542', '-0.4336', '0.0827', '-0.1299', '0.0374', '-0.02829', '-0.07715', '0.1351', '0.1217', '-0.1152', '0.2361', '-0.1672', '-0.139', '0.0722', '0.2603', '0.4875', '-0.156', '-0.2281', '0.2673', '-0.08124', '-0.01002', '0.476', '0.3298', '-0.1488', '-0.0476', '-0.1567', '0.1466', '0.5234', '0.232', '0.08203', '-0.2478', '-0.2411', '0.0699']",,,C536106,756.89,,,
mondo:0013599,autoimmune enteropathy and endocrinopathy - susceptibility to chronic infections syndrome,"['candidiasis familial, 7', 'IMD31C', 'immunodeficiency 31C, chronic mucocutaneous candidiasis, autosomal dominant', 'candidiasis familial chronic mucocutaneous, autosomal dominant', 'candidiasis, familial, 7', 'immunodeficiency 31C', 'candidiasis, familial chronic mucocutaneous, autosomal dominant', 'immunodeficiency type 31C', 'CANDF7', 'familial chronic mucocutaneous, autosomal dominant']",0111946,614162,391487,C3279990,"['0.1532', '0.4656', '0.325', '-0.8447', '0.175', '-0.3572', '0.2732', '-0.2', '-0.02557', '-0.34', '0.0088', '0.2443', '-0.05753', '-0.2258', '-0.073', '-0.1144', '0.2001', '0.2942', '-0.4275', '-0.726', '0.2487', '-0.3596', '0.3618', '-0.5156', '-0.117', '0.2854', '-0.0628', '0.2031', '0.6226', '-1.418', '0.4595', '0.252', '0.6006', '0.345', '-0.0583', '0.1007', '-0.755', '-0.03075', '-0.2218', '-0.01102', '-0.484', '0.363', '0.4824', '0.365', '-0.06155', '-0.6006', '0.6235', '0.0657', '0.0753', '-0.08545', '0.1383', '0.639', '-0.1076', '-0.2454', '-0.1322', '-0.2683', '-0.09814', '-0.4724', '-0.3982', '-0.1755', '0.221', '0.9097', '0.173', '0.1558', '0.623', '0.1627', '0.2245', '0.4026', '-0.3662', '0.734', '-0.6953', '-0.2864', '0.03372', '-0.1886', '0.2125', '-0.1649', '0.2783', '0.5137', '0.0914', '-0.07874', '-0.05585', '-0.1165', '0.03665', '0.4014', '-0.012184', '0.2463', '0.674', '0.3496', '0.4854', '0.1515', '0.1752', '0.4438', '0.01539', '-0.6562', '0.8755', '0.639', '0.3616', '-0.11707', '-0.2795', '0.2274']",,,,,,,
mondo:0013600,insomnia,"['insomnia', 'DSPS', 'insomnia (disease)', 'delayed sleep phase disorder, susceptibility to', 'DSPD', 'delayed sleep phase syndrome, susceptibility to']",,,,C0393770,"['0.2505', '0.3105', '-0.3638', '0.4363', '-0.4023', '-0.0521', '-0.0104', '1.096', '0.0274', '0.0856', '0.528', '0.2651', '-0.02287', '0.809', '-0.6216', '-0.7993', '-0.5576', '0.4177', '-0.796', '-0.6753', '-0.4937', '-0.5215', '0.01949', '-0.2551', '0.0708', '-0.7026', '0.1743', '-0.173', '0.0882', '0.1864', '0.534', '-0.3823', '0.02206', '0.777', '-0.2065', '-0.2188', '-0.646', '-0.1332', '0.2361', '-0.3987', '0.6484', '0.2031', '-0.2446', '0.3513', '0.3064', '-0.9204', '-0.2556', '0.2944', '0.388', '1.104', '-0.2457', '0.857', '-0.3054', '0.25', '0.483', '-0.0826', '0.148', '0.5464', '-0.509', '-0.986', '-0.04626', '1.069', '0.2351', '-0.1361', '-0.06384', '0.733', '0.002369', '0.5215', '0.1145', '0.2546', '-0.0979', '0.3489', '0.2678', '-0.659', '0.3555', '0.1015', '0.2856', '0.808', '-0.2822', '-0.3591', '-0.148', '0.03204', '-0.1809', '0.651', '0.855', '0.2032', '0.04126', '0.1412', '0.9907', '0.3809', '-0.1838', '0.0479', '-0.8506', '0.2607', '-0.49', '0.1328', '-0.5435', '-0.3132', '-0.397', '-0.1451']",C28286,0004698,D007319,780.52,G47.0,,0100785
mondo:0013601,gluthathione peroxidase deficiency,"['GPXD', 'hemolytic anemia due to glutathione peroxidase deficiency', 'hemolytic anaemia due to glutathione peroxidase deficiency', 'glutathione peroxidase deficiency']",,614164,,C0398747,,,,,,,,
mondo:0013602,paragangliomas 5,"['paragangliomas type 5', 'paraganglioma caused by mutation in SDHA', 'PGL5', 'paragangliomas 5', 'SDHA paraganglioma']",,614165,,C3279992,,,,,,,,
mondo:0013603,"myopia 20, autosomal dominant","['MYP20', 'myopia 20, autosomal dominant']",,614166,,C3279996,,,,,,,,
mondo:0013604,"myopia 21, autosomal dominant","['myopia 21, autosomal dominant', 'ZNF644 myopia (disease)', 'MYP21']",,614167,,C3279997,,,,,,,,
mondo:0013605,brittle cornea syndrome 2,"['PRDM5 brittle cornea syndrome', 'brittle cornea syndrome caused by mutation in PRDM5', 'brittle cornea syndrome type 2', 'brittle cornea syndrome 2', 'BCS2']",0080729,614170,,C3280011,,,,,,,,
mondo:0013606,Hermansky-Pudlak syndrome 9,"['Hermansky-Pudlak syndrome caused by mutation in BLOC1S6', 'Hermansky-Pudlak syndrome type 9', 'BLOC1S6 Hermansky-Pudlak syndrome', 'Hermansky-Pudlak syndrome 9', 'HPS9']",0060547,614171,280663,C3280026,"['-0.1018', '0.2695', '-0.03696', '0.1101', '0.2006', '-0.2223', '-0.113', '0.0611', '-0.1915', '-0.03238', '-0.01988', '-0.0729', '-0.0363', '0.1237', '0.0507', '-0.2219', '0.1364', '0.1543', '0.07214', '-0.3528', '0.02792', '-0.09546', '0.0429', '-0.1426', '0.1324', '0.08167', '-0.0425', '0.2091', '0.10376', '0.013', '0.2434', '0.01718', '0.1876', '0.0089', '0.1233', '-0.02655', '0.01522', '-0.162', '0.0981', '-0.2703', '0.3591', '-0.3035', '0.002659', '-0.1488', '-0.1552', '-0.442', '0.06476', '0.1135', '0.2673', '-0.11224', '-0.0702', '-0.0917', '0.1508', '0.1396', '-0.2029', '-0.2595', '0.355', '0.07623', '-0.2966', '-0.2476', '0.03275', '0.0582', '0.12225', '0.05988', '0.06143', '0.1555', '0.2078', '-0.1066', '-0.2136', '0.2012', '-0.315', '-0.0935', '0.01785', '-0.02254', '0.1685', '-0.02039', '0.03604', '-0.013985', '-0.0837', '0.04742', '-0.0351', '-0.0981', '0.1375', '0.09814', '-0.1526', '-0.3833', '0.309', '0.4995', '0.2317', '0.2335', '0.10785', '0.1434', '0.09326', '-0.134', '0.4788', '0.11194', '0.0962', '-0.3206', '0.01458', '0.08905']",,,,,E70.3,,
mondo:0013607,monocytopenia with susceptibility to infections,"['Dendritic cell, monocyte, B lymphocyte, and natural Killer lymphocyte deficiency', 'MonoMAC', 'immunodeficiency 21', 'monocytopenia and mycobacterial infection syndrome', 'immunodeficiency type 21', 'DCML', 'monocyte-B-natural killer-dendritic cell deficiency syndrome', 'IMD21', 'combined immunodeficiency with susceptibility to mycobacterial, viral, and fungal infections', 'monocytopenia with susceptibility to mycobacterial, fungal, and Papillomavirus infections and myelodysplasia', 'combined immunodeficiency with susceptibility to mycobacterial, viral and fungal infections', 'Dendritic cell, monocyte, B and NK lymphoid deficiency', 'monocyte - B - natural killer - dendritic cell deficiency', 'GATA2 deficiency']",0111947,614172,228423,C3280030,"['-0.304', '-0.1396', '0.1875', '-0.4346', '0.2064', '-0.4287', '0.3103', '0.07965', '0.00786', '-0.3494', '0.10333', '0.2379', '-0.1992', '-0.1942', '0.1677', '-0.2053', '0.1194', '0.1064', '-0.1544', '-0.5757', '-0.0998', '-0.119', '0.7397', '-0.479', '0.00973', '-0.07806', '-0.1348', '0.0511', '-0.2133', '-0.5327', '0.1615', '0.3606', '0.4673', '-0.05078', '0.193', '-0.2593', '-0.7812', '-0.149', '-0.308', '-0.5366', '-0.2505', '-0.1192', '0.2397', '-0.3867', '-0.538', '-0.2842', '-0.2056', '-0.2037', '0.167', '0.1646', '0.0755', '0.003067', '0.2712', '0.1841', '-0.0866', '0.1941', '0.326', '-0.481', '-0.2261', '0.0667', '-0.1337', '0.651', '0.09033', '-0.2032', '0.5635', '0.01317', '0.2988', '0.4187', '-0.2124', '0.565', '-0.3867', '-0.1918', '0.05707', '0.02475', '0.01611', '-0.561', '0.4094', '0.1552', '0.4055', '0.02826', '-0.3752', '0.1228', '0.1582', '0.2952', '-0.4695', '-0.3704', '0.4868', '0.4429', '0.3408', '-0.03857', '0.2505', '0.4758', '-0.254', '-0.3376', '0.65', '0.7437', '0.6665', '-0.6196', '-0.1962', '-0.09326']",,,,,,,
mondo:0013608,Joubert syndrome 13,"['Joubert syndrome type 13', 'TCTN1 Joubert syndrome', 'Joubert syndrome caused by mutation in TCTN1', 'JBTS13', 'Joubert syndrome 13']",0110982,614173,,C3280031,,,,,,,,
mondo:0013609,"Meckel syndrome, type 10","['B9D2 Meckel syndrome', 'JBTS34', 'Meckel syndrome, type 10', 'Meckel syndrome caused by mutation in B9D2', 'meckel syndrome 10', 'Joubert syndrome 34', 'MKS10']",,614175,,CN620433,,,,,,,,
mondo:0013610,retinitis pigmentosa 61,"['retinitis pigmentosa caused by mutation in CLRN1', 'RP61', 'retinitis pigmentosa 61', 'retinitis pigmentosa type 61', 'CLRN1 retinitis pigmentosa']",0110373,614180,,C3280041,,,,,,H35.5,,
mondo:0013611,retinitis pigmentosa 62,"['MAK retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in MAK', 'retinitis pigmentosa type 62', 'RP62', 'retinitis pigmentosa 62']",0110380,614181,,C3280042,,,,,,H35.5,,
mondo:0013612,geleophysic dysplasia 2,"['geleophysic dysplasia caused by mutation in FBN1', 'Geleophysic dysplasia 2', 'GELEOPHYSIC dysplasia 2', 'GPHYSD2', 'FBN1 geleophysic dysplasia', 'Geleophysic dysplasia type 2']",0111726,614185,,C3280054,,,,,,,,
mondo:0013613,Leber congenital amaurosis 16,"['Leber congenital amaurosis type 16', 'KCNJ13 Leber congenital amaurosis', 'LCA16', 'Leber congenital amaurosis 16', 'Leber congenital amaurosis caused by mutation in KCNJ13']",0110118,614186,,C3280062,,,,,,H35.5,,
mondo:0013614,hypertelorism-preauricular sinus-punctual pits-deafness syndrome,"['HPPD', 'hypertelorism, preauricular sinus, punctal pits, and deafness', 'hypertelorism-preauricular sinus-punctual pits-hearing loss syndrome']",,614187,293958,C3280065,,,,,,,,
mondo:0013615,craniosynostosis and dental anomalies,"['craniosynostosis and dental anomalies', 'craniosynostosis-dental anomalies', 'CRSDA', 'Kreiborg-Pakistani syndrome']",,614188,284149,C3280073,"['0.4893', '-0.2893', '-0.02376', '0.1099', '0.344', '-0.2328', '-0.04465', '0.769', '-0.8657', '-0.3867', '-0.06683', '-0.4136', '0.1886', '0.5874', '-0.3948', '-0.214', '0.67', '-0.6514', '-0.0804', '-1.118', '0.04068', '1.036', '0.3274', '-0.237', '1.126', '0.6978', '-0.2866', '-0.202', '0.717', '0.291', '0.02927', '0.4014', '-0.1924', '-0.486', '-0.2869', '0.0748', '-0.2954', '-0.4102', '-0.3396', '-0.9834', '0.4949', '0.2651', '-0.2732', '-0.921', '0.492', '-0.4287', '0.0246', '0.01161', '0.4197', '-0.3027', '-0.1148', '-0.1315', '-0.05365', '-0.1504', '-0.3052', '-0.3958', '-0.628', '0.05652', '-0.5864', '0.2202', '-0.3364', '-0.09424', '0.09125', '0.4514', '-0.1805', '0.3933', '-0.3596', '0.7393', '-0.03096', '0.916', '-0.2778', '1.283', '0.1843', '-0.8574', '-0.401', '0.4158', '0.3499', '0.333', '-0.944', '-0.562', '0.3564', '0.04788', '-0.4036', '0.3179', '0.2288', '0.02603', '-0.1414', '0.12396', '0.501', '0.759', '-0.7495', '0.1273', '-0.107', '0.2988', '0.3987', '0.1371', '0.1018', '-0.2496', '0.979', '-0.11743']",,,,,,,
mondo:0013616,"pigmented nodular adrenocortical disease, primary, 3","['PDE8B primary pigmented nodular adrenocortical disease', 'pigmented nodular adrenocortical disease, primary, 3', 'primary pigmented nodular adrenocortical disease caused by mutation in PDE8B', 'PPNAD3', 'Cushing syndrome, adrenal, due to PPNAD3', 'pigmented nodular adrenocortical disease, primary, type 3']",,614190,,C3280094,,,,,,,,
mondo:0013618,craniofacial anomalies and anterior segment dysgenesis syndrome,"['craniofacial anomalies and anterior segment dysgenesis syndrome', 'CAASDS']",,614195,,C3280099,"['-0.04053', '0.04596', '0.02666', '-0.00908', '0.01484', '-0.0528', '0.00369', '0.06134', '-0.0675', '-0.05185', '-0.02974', '-0.02658', '0.0009575', '0.01157', '-0.0407', '-0.0336', '-0.002056', '-0.01735', '-0.0261', '-0.1138', '0.01619', '-0.0231', '0.0624', '-0.02963', '0.02095', '-0.01442', '-0.01663', '0.007183', '0.02487', '-0.039', '0.04788', '0.003311', '0.05716', '0.005436', '0.01347', '-0.02597', '-0.01201', '-0.0386', '-0.01214', '-0.0766', '0.0361', '-0.05643', '0.01819', '-0.0326', '0.004543', '-0.03818', '-0.01437', '0.02797', '0.00581', '0.003769', '-0.01692', '0.001509', '0.004303', '0.003763', '-0.03072', '-0.03613', '0.04837', '-0.0232', '-0.0648', '0.003778', '0.05438', '0.01686', '-0.01018', '0.01947', '-0.00869', '0.00836', '0.07715', '0.05554', '-0.05292', '0.06018', '-0.0665', '0.03903', '0.01912', '-0.02263', '-0.003162', '0.02153', '0.02136', '-0.02585', '-0.0504', '-0.03375', '-0.010056', '0.01584', '-0.02107', '0.06793', '-0.01881', '-0.002722', '0.01364', '0.06094', '0.05325', '0.005207', '0.009964', '0.05927', '0.00904', '0.01747', '0.1231', '0.000746', '0.0684', '-0.0678', '-0.0006523', '0.03156']",,,,,,,
mondo:0013619,"nephrotic syndrome, type 6","['PTPRO nephrotic syndrome', 'NPHS6', 'nephrotic syndrome, type 6', 'nephrotic syndrome caused by mutation in PTPRO']",0080384,614196,,C3280100,,,,,,,,
mondo:0013620,congenital myasthenic syndrome 16,"['CMS16', 'myasthenic syndrome, congenital, type 16', 'myasthenic syndrome, congenital, Acetazolamide-responsive', 'SCN4A congenital myasthenic syndrome', 'congenital myasthenic syndrome type 16', 'myasthenic syndrome, congenital, 16', 'congenital myasthenic syndrome acetazolamide-responsive', 'congenital myasthenic syndrome caused by mutation in SCN4A']",0110682,614198,,,,,,,,,,
mondo:0013621,LAMB2-related infantile-onset nephrotic syndrome,"['NPHS5', 'nephrotic syndrome, type 5, with or without ocular abnormalities']",0080380,614199,306507,C3280113,"['0.6523', '-0.387', '0.1715', '0.09595', '-0.387', '-0.51', '0.2251', '0.07294', '-0.6646', '-0.317', '0.4146', '0.04126', '-0.6616', '0.728', '-0.7744', '-0.1023', '0.1486', '0.7144', '0.63', '-0.8457', '0.7847', '-0.696', '0.0525', '0.6035', '-0.03085', '-0.3499', '-0.59', '0.3809', '0.1417', '-0.1704', '0.729', '-0.1388', '1.079', '0.0923', '-0.29', '-0.2345', '-0.1255', '0.2167', '0.1451', '-0.596', '-0.1562', '0.2734', '-0.2141', '-0.4846', '-0.359', '-0.1646', '0.3418', '-0.09216', '0.2136', '-0.3545', '-0.3699', '0.5273', '1.079', '-0.649', '-0.0704', '-0.6123', '0.11237', '0.1076', '-1.007', '-0.1384', '-0.586', '-0.3704', '0.242', '-0.3867', '-0.1782', '-0.05334', '0.8315', '0.3516', '-0.86', '0.2874', '-0.662', '0.5864', '0.3555', '-0.2404', '0.1542', '-0.0325', '0.33', '0.7637', '-0.1539', '0.4526', '-0.3442', '-0.2202', '-0.1819', '-0.004738', '-0.04813', '-0.3457', '-0.04715', '-0.1675', '0.4485', '0.7373', '0.3389', '0.7305', '-0.64', '-0.2556', '0.2754', '0.7026', '-0.4333', '-0.588', '-0.124', '-0.1826']",,,,,,,
mondo:0013622,platelet-type bleeding disorder 9,"['bleeding diathesis due to integrin alpha2-beta1 deficiency', 'GP Ia deficiency', 'glycoprotein Ia deficiency', 'bleeding disorder, platelet-type, 9', 'BDPLT9', 'ITGA2 inherited bleeding disorder, platelet-type', 'inherited bleeding disorder, platelet-type caused by mutation in ITGA2', 'collagen platelet receptor deficiency']",0111045,614200,98886,,,,,C566000,,,,
mondo:0013623,platelet-type bleeding disorder 11,"['GP 6 deficiency', 'bleeding diathesis due to glycoprotein VI deficiency', 'glycoprotein VI deficiency', 'inherited bleeding disorder, platelet-type caused by mutation in GP6', 'glycoprotein 6 deficiency', 'platelet-type bleeding disorder-11', 'GP VI deficiency', 'bleeding disorder, platelet-type, 11', 'BDPLT11', 'GP6 inherited bleeding disorder, platelet-type']",0111057,614201,98885,C3280120,"['-0.3574', '-0.0419', '-0.2158', '-0.09607', '0.03122', '-0.01373', '-0.1207', '-0.2979', '0.0847', '-0.04553', '0.5405', '-0.0655', '0.2213', '-0.0816', '0.0488', '-0.2925', '-0.1394', '0.1144', '-0.0977', '-0.4556', '0.2092', '-0.1904', '0.2666', '-0.04358', '0.05078', '0.0665', '-0.1334', '-0.05856', '0.2507', '0.3337', '0.1842', '0.041', '0.3042', '0.2251', '-0.291', '-0.301', '-0.1451', '0.02882', '0.3032', '-0.5444', '-0.2257', '-0.02881', '0.08655', '-0.10547', '0.1765', '-0.4497', '0.13', '-0.02362', '0.5083', '0.1681', '0.1132', '-0.2462', '0.3428', '0.3875', '-0.136', '0.03607', '0.277', '-0.0196', '-0.4084', '0.0991', '-0.134', '0.1555', '0.2489', '-0.2', '0.2003', '0.0846', '0.1675', '0.01248', '-0.708', '0.4824', '-0.444', '-0.0103', '-0.1472', '-0.626', '0.2854', '0.1837', '0.6416', '0.3777', '0.4287', '0.03516', '-0.329', '-0.2925', '0.1708', '-0.1938', '-0.2479', '0.0737', '0.05344', '0.3708', '0.2234', '0.01408', '0.0714', '0.2966', '-0.00874', '-0.0869', '0.4824', '0.627', '0.2542', '-0.2493', '-0.292', '0.1298']",,,,,,,
mondo:0013624,Rafiq syndrome,"['mental retardation, autosomal recessive 15', 'CDG2U', 'MAN1B1 autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive type 15', 'RAFQS', 'intellectual disability, autosomal recessive 15', 'autosomal recessive non-syndromic intellectual disability caused by mutation in MAN1B1', 'MRT15']",0081097,614202,,C3280127,,,,,,,,
mondo:0013625,Parkinson disease 17,"['PARK17', 'Parkinson^s disease 17', 'autosomal dominant Parkinson disease 17', 'Parkinson disease type 17', 'VPS35 Parkinson disease', 'Parkinson disease 17', 'Parkinson disease caused by mutation in VPS35']",0060897,614203,,C3280133,,,,,,,,
mondo:0013626,"psoriasis 14, pustular","['familial generalised pustular psoriasis', 'GPP', 'generalized pustular psoriasis', 'deficiency of IL-36R antagonist', 'Interleukin 36 receptor antagonist deficiency', 'palmoplantar pustulosis', 'PSORS14', 'acrodermatitis continua suppurativa of Hallopeau', 'deficiency of IL-36Ra', 'generalised pustular psoriasis', 'deficiency of the interleukin-36 receptor antagonist', 'psoriasis 14, pustular', 'familial generalized pustular psoriasis', 'PSORP', 'acrodermatitis continua of Hallopeau', 'psoriasis caused by mutation in IL36RN', 'IL36RN psoriasis', 'DITRA']",0080474,614204,404546,CN226196,"['-0.0251', '0.04352', '-0.01521', '-0.001986', '0.01616', '-0.0744', '-0.00663', '0.03467', '-0.0232', '0.000797', '-0.009544', '0.01837', '0.00873', '-0.001786', '-0.013374', '-0.02736', '0.01296', '-0.02725', '-0.004845', '-0.07635', '0.003124', '-0.01463', '0.02591', '-0.0166', '0.00506', '0.002575', '-0.003202', '0.01246', '-0.001875', '-0.02322', '0.0313', '-0.01581', '0.02756', '0.02692', '0.00739', '0.00269', '-0.01959', '-0.02281', '-0.00488', '-0.04425', '0.0233', '-0.0488', '0.00129', '0.002726', '0.01449', '-0.03632', '-0.01898', '0.0288', '0.01126', '0.02553', '-0.01985', '-0.0166', '-0.00951', '0.007298', '-0.006798', '-0.01133', '0.03485', '-0.04428', '-0.0479', '-0.002747', '0.01464', '0.005775', '0.005714', '0.00261', '0.00458', '-0.001247', '0.06207', '0.0182', '-0.03445', '0.063', '-0.0293', '-0.01921', '0.01274', '-0.03683', '0.02061', '0.03008', '-0.013336', '0.01968', '-0.01741', '-0.02728', '-0.01272', '-0.006695', '-0.01724', '0.02684', '0.00694', '0.01439', '-0.00464', '0.067', '0.05157', '0.01142', '0.00973', '0.03516', '0.007336', '0.017', '0.09534', '0.02374', '0.02484', '-0.0675', '0.002254', '0.0004227']",C119057,,,696.1,,,
mondo:0013627,3M syndrome 3,"['3M syndrome 3', 'three M syndrome 3', '3-M syndrome caused by mutation in CCDC8', 'CCDC8 3-M syndrome', 'three M syndrome type 3', '3M3', '3-M syndrome 3']",,614205,,C3280146,,,,,,,,
mondo:0013628,hyperphosphatasia with intellectual disability syndrome 3,"['hyperphosphatasia with intellectual disability syndrome type 3', 'intellectual disability, autosomal recessive 21', 'PGAP2 hyperphosphatasia-intellectual disability syndrome', 'hyperphosphatasia-intellectual disability syndrome caused by mutation in PGAP2', 'glycosylphosphatidylinositol biosynthesis defect 8', 'mental retardation, autosomal recessive 17', 'intellectual disability, autosomal recessive 17', 'hyperphosphatasia with mental retardation syndrome type 3', 'mental retardation, autosomal recessive 21', 'hyperphosphatasia with mental retardation syndrome 3', 'hyperphosphatasia with intellectual disability syndrome 3', 'HPMRS3']",,614207,,C3280153,,,,,,,,
mondo:0013629,"intellectual disability, autosomal recessive 16","['intellectual disability, autosomal recessive 16', 'MRT16', 'mental retardation, autosomal recessive 16']",0081189,614208,,C3280154,,,,,,,,
mondo:0013630,"Meckel syndrome, type 9","['meckel syndrome 9', 'Meckel syndrome, type 9', 'B9D1 Meckel syndrome', 'MKS9', 'Meckel syndrome caused by mutation in B9D1']",,614209,,C3280155,,,,,,,,
mondo:0013631,lung cancer susceptibility 5,"['LNCR5', 'lung cancer susceptibility 5']",,614210,,C3280156,,,,,,,,
mondo:0013632,autosomal dominant nonsyndromic hearing loss 33,"['deafness, autosomal dominant 33', 'autosomal dominant nonsyndromic deafness type 33', 'autosomal dominant deafness 33', 'autosomal dominant nonsyndromic deafness 33', 'DFNA33']",0110562,614211,,,,,,,,,,
mondo:0013633,"encephalopathy, acute, infection-induced, susceptibility to, 4","['encephalopathy, acute, infection-induced, 4, susceptibility to', 'IIAE4', 'encephalopathy, acute, infection-induced, susceptibility to, 4', 'CPT2 encephalopathy, acute, infection-induced', 'encephalopathy, acute, infection-induced caused by mutation in CPT2', 'encephalopathy, acute, infection-induced, susceptibility to, type 4']",,614212,,,,,,,,,,
mondo:0013634,"neuropathy, hereditary sensory, type 2C","['KIF1A hereditary sensory and autonomic neuropathy type 2', 'hereditary sensory neuropathy type IIC', 'hereditary sensory and autonomic neuropathy type 2 caused by mutation in KIF1A', 'HSN2C', 'neuropathy, hereditary sensory, type IIC', 'hereditary sensory neuropathy type 2C']",0070147,614213,,C3280168,,,,,,,,
mondo:0013635,Adams-Oliver syndrome 2,"['Adams-Oliver syndrome caused by mutation in DOCK6', 'AOS2', 'Adams-Oliver syndrome 2', 'Adams-Oliver syndrome type 2', 'DOCK6 Adams-Oliver syndrome']",,614219,,C3280182,,,,,,,,
mondo:0013636,primary biliary cholangitis 4,"['PBC4', 'biliary cirrhosis, primary, 4']",0070361,614220,,C3280201,,,,,,,,
mondo:0013637,primary biliary cholangitis 5,"['PBC5', 'biliary cirrhosis, primary, 5']",0070362,614221,,C3280202,,,,,,,,
mondo:0013638,Warburg micro syndrome 3,"['Warburg micro syndrome 3', 'WARBURG micro syndrome 3', 'Warburg micro syndrome type 3', 'Warburg micro syndrome caused by mutation in RAB18', 'WARBM3', 'RAB18 Warburg micro syndrome', 'micro syndrome 3']",0110718,614222,,C3280203,,,,,,,,
mondo:0013639,"narcolepsy 6, susceptibility to","['narcolepsy 6, susceptibility to', 'NRCLP6', 'narcolepsy 6']",,614223,,,,,,,,,,
mondo:0013640,familial retinal arterial macroaneurysm,"['retinal arterial macroaneurysm with supravalvular pulmonic stenosis', 'RAMSVPS', 'retinal arterial macroaneurysm and supravalvular pulmonic stenosis', 'Fram']",,614224,284247,C3280205,"['-0.398', '-0.149', '0.0722', '-0.009674', '0.0996', '-0.3286', '0.1642', '0.33', '-0.3323', '-0.2386', '-0.1218', '-0.3796', '0.0494', '0.05914', '-0.315', '-0.4167', '-0.1462', '0.0822', '-0.0645', '-0.429', '0.01128', '-0.012184', '-0.05078', '0.1189', '0.03195', '0.0791', '0.02763', '0.3164', '0.2957', '0.3767', '0.513', '0.297', '0.11664', '0.1255', '-0.004482', '-0.07605', '0.4946', '0.01605', '0.5264', '-0.4924', '0.4905', '0.07', '0.531', '0.04117', '-0.0633', '0.0934', '-0.01907', '0.04694', '0.1984', '-0.0374', '0.08545', '0.1294', '0.3572', '0.006004', '-0.3125', '-0.3938', '0.453', '0.04956', '-0.1539', '0.177', '0.2439', '0.3047', '0.1783', '-0.3147', '0.3333', '-0.05106', '0.1727', '0.353', '-0.2883', '0.3088', '-0.3755', '-0.03503', '0.04834', '-0.145', '-0.05032', '-0.369', '0.1815', '0.3538', '-0.1581', '-0.004013', '-0.1268', '-0.1143', '-0.1815', '0.2842', '-0.218', '-0.1881', '0.4204', '0.3015', '0.2478', '0.06256', '-0.001878', '0.2474', '-0.00248', '-0.0532', '0.6147', '-0.1045', '0.592', '-0.484', '-0.2401', '0.3315']",,,,,,,
mondo:0013641,Warburg micro syndrome 2,"['Warburg micro syndrome 2', 'Warburg micro syndrome type 2', 'RAB3GAP2 Warburg micro syndrome', 'micro syndrome 2', 'WARBURG micro syndrome 2', 'WARBM2', 'Warburg micro syndrome caused by mutation in RAB3GAP2']",0110717,614225,,C3280214,,,,,,,,
mondo:0013642,holoprosencephaly 11,"['holoprosencephaly 11', 'holoprosencephaly caused by mutation in CDON', 'holoprosencephaly type 11', 'CDON holoprosencephaly', 'HPE11']",0110877,614226,,C3280215,,,,,,,,
mondo:0013643,"hyperuricemic nephropathy, familial juvenile type 3","['HNFJ3', 'hyperuricemic nephropathy, familial juvenile, 3']",,614227,,C3280216,,,,,,,,
mondo:0013644,Charcot-Marie-Tooth disease axonal type 2O,"['Charcot-Marie-Tooth disease, axonal, type 20', 'Charcot-Marie-Tooth disease type 2O', 'Charcot-Marie-Tooth neuropathy, axonal, type 2O', 'DYNC1H1 Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth disease caused by mutation in DYNC1H1', 'CMT2O', 'autosomal dominant Charcot-Marie-Tooth disease type 2O', 'Charcot-Marie-Tooth disease, axonal, type 2O', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2O', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2O', 'Charcot-Marie-Tooth neuropathy axonal type 2O']",0110175,614228,284232,C3280220,"['0.1055', '0.2124', '0.2795', '-0.08923', '0.001494', '-0.4912', '0.2537', '0.572', '-0.821', '-0.11255', '0.1404', '0.3677', '-0.6465', '0.4631', '0.0407', '0.03223', '-0.1528', '-0.248', '-0.634', '-0.646', '0.2554', '0.389', '0.1562', '0.5522', '0.2644', '0.246', '-0.01988', '0.03134', '-0.0696', '-0.2888', '0.3774', '-0.6763', '0.2211', '-0.0537', '0.155', '-0.6743', '-0.663', '-0.2705', '0.581', '0.0669', '-0.9346', '-0.299', '-0.44', '0.4531', '-0.04904', '-0.409', '0.491', '-0.2081', '-0.0965', '-0.02255', '0.07184', '0.3718', '-0.4658', '-1.004', '0.1975', '-0.1823', '-0.518', '0.2023', '-0.6597', '-0.1903', '-0.3088', '0.1295', '0.7095', '0.6455', '-0.7397', '1.058', '-0.05948', '0.756', '-0.566', '0.327', '-0.711', '0.189', '0.606', '-0.3652', '1.147', '0.3718', '-0.2927', '0.5293', '0.0433', '-0.3794', '-0.03998', '-0.3042', '0.815', '0.672', '-0.11', '-0.0809', '0.3184', '0.3848', '0.5435', '0.408', '0.1703', '-0.0747', '-0.1268', '0.3904', '0.4265', '0.3906', '0.639', '-0.739', '0.0488', '0.717']",,,,,,,
mondo:0013645,autosomal recessive spinocerebellar ataxia 11,"['SYT14 autosomal recessive syndromic cerebellar ataxia', 'SCAR11', 'autosomal recessive spinocerebellar ataxia type 11', 'autosomal recessive cerebellar ataxia-psychomotor retardation syndrome', 'spinocerebellar ataxia, autosomal recessive 11', 'autosomal recessive syndromic cerebellar ataxia caused by mutation in SYT14', 'spinocerebellar ataxia, autosomal recessive type 11']",0080063,614229,284271,C3280226,"['-0.2263', '-0.351', '0.1548', '0.02275', '-0.09247', '-1.085', '0.1528', '0.1271', '-0.7', '-0.921', '0.1235', '0.2815', '-0.248', '0.0741', '0.3982', '-0.3606', '-0.1466', '-0.3435', '-0.01985', '-1.101', '-0.06247', '-0.334', '0.079', '-0.658', '0.572', '-0.662', '-0.2617', '0.1578', '-0.2197', '-0.861', '0.02707', '0.4675', '-0.4194', '-0.1572', '0.4763', '0.1879', '-0.3347', '-0.05597', '0.4653', '0.1927', '0.3455', '0.3198', '-0.5864', '0.4304', '0.532', '-0.5522', '0.1057', '0.44', '0.4316', '-0.001455', '-0.2219', '0.1816', '-0.04932', '-0.4504', '-0.1823', '-0.8394', '0.2404', '0.5684', '-0.1652', '0.619', '-0.5854', '0.2917', '0.3416', '-0.1926', '-0.535', '0.5806', '0.2434', '0.6123', '-0.604', '0.4224', '0.9707', '0.584', '-0.1032', '-0.6504', '0.7227', '0.355', '0.3154', '0.423', '0.298', '0.5107', '-0.522', '-0.767', '0.321', '0.779', '-0.3286', '-0.7046', '0.1368', '0.09216', '0.534', '0.6396', '0.381', '0.444', '-0.0975', '0.04318', '1.06', '1.128', '0.3413', '0.3955', '-0.2683', '0.03375']",,,,,,,
mondo:0013646,chromosome 8q21.11 deletion syndrome,"['deletion 8q21.11', '8q21.11 microdeletion syndrome', 'chromosome 8q21.11 deletion syndrome', 'Del(8)(q21.11)', 'chromosome 8q21.11 deletion syndrome, isolated cases', 'monosomy 8q21.11']",0060425,614230,284160,C4305343,,,,,,,,
mondo:0013648,familial progressive hyperpigmentation,"['FPH1', 'Fph', 'melanosis universalis hereditaria', 'universal melanosis', 'hyperpigmentation, familial progressive, 1', 'melanosis diffusa congenita']",,614233,79146,CN205811,"['-0.04962', '0.0983', '-0.3262', '-0.03983', '0.346', '-0.2751', '-0.342', '0.108', '-0.766', '-0.1238', '-0.05334', '0.32', '-0.4536', '0.1472', '0.0402', '0.1376', '0.345', '0.04385', '-0.089', '-0.634', '-0.3765', '-0.1237', '0.2323', '-0.3005', '0.01837', '0.357', '-0.1964', '0.1508', '-0.2563', '-0.1827', '0.593', '-0.4768', '0.04788', '0.398', '0.02231', '0.418', '-0.2874', '0.0779', '0.1658', '-0.10065', '0.03696', '-0.2222', '0.131', '0.09656', '0.0709', '-0.526', '-0.1873', '0.4072', '0.291', '0.05548', '0.05945', '0.08655', '0.3545', '-0.0475', '-0.3071', '-0.217', '0.1964', '0.05057', '-0.233', '-0.5386', '-0.1483', '0.133', '-0.355', '-0.3596', '-0.003607', '0.3223', '0.5884', '0.7607', '0.0754', '0.742', '-0.07776', '0.04614', '-0.03967', '0.06976', '0.3691', '0.1285', '-0.2036', '0.01854', '-0.0826', '-0.4912', '-0.2167', '-0.04175', '0.166', '-0.04282', '-0.000151', '-0.4077', '0.02997', '-0.01085', '0.1578', '0.0422', '0.149', '0.1552', '0.118', '-0.1254', '0.308', '0.0636', '0.4463', '0.02322', '0.1776', '0.0519']",,,,,,,
mondo:0013649,hypotrichosis 9,"['HYPT9', 'hypt9', 'hypotrichosis 9', 'hypotrichosis type 9']",0110706,614237,,C3280252,,,,,,,,
mondo:0013650,hypotrichosis 10,"['hypotrichosis 10', 'hypotrichosis type 10', 'HYPT10', 'hypt10']",0110707,614238,,C3280253,,,,,,,,
mondo:0013651,"intellectual disability, autosomal recessive 18","['MED23 autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive type 18', 'MRT18', 'MED23', 'intellectual disability, autosomal recessive 18', 'autosomal recessive nonsyndromic mental retardation-18', 'autosomal recessive non-syndromic intellectual disability caused by mutation in MED23', 'autosomal recessive nonsyndromic intellectual disability-18', 'mental retardation, autosomal recessive 18', 'intellectual developmental disorder, autosomal recessive 18, with or without epilepsy', 'intellectual disability, autosomal recessive type 18']",0081190,614249,,C3280265,,,,,,,,
mondo:0013652,narcolepsy 7,"['narcolepsy 7', 'narcolepsy type 7', 'MOG narcolepsy', 'narcolepsy caused by mutation in MOG', 'NRCLP7']",,614250,,C3280266,,,,,,,,
mondo:0013653,"Parkinson disease 18, autosomal dominant, susceptibility to","['susceptibility to autosomal dominant Parkinson disease 18', 'Parkinson disease 18, autosomal dominant, susceptibility to', 'Parkinson disease 18', 'EIF4G1 hereditary late onset Parkinson disease', 'PARK18', 'hereditary late onset Parkinson disease caused by mutation in EIF4G1']",,614251,,C3280271,,,,,,,,
mondo:0013654,"aneurysm, intracranial berry, 11","['aneurysm, intracranial BERRY, 11', 'ANIB11']",0080974,614252,,C3280275,,,,,,,,
mondo:0013655,"intellectual disability, autosomal dominant 8","['MRD8', 'intellectual disability, autosomal dominant 8', 'intellectual disability, autosomal dominant type 8', 'mental retardation, autosomal dominant 8', 'mental retardation, autosomal dominant type 8', 'autosomal dominant mental retardation 8', 'autosomal dominant non-syndromic intellectual disability 8', 'mental retardation, autosomal dominant 8, formerly', 'neurodevelopmental disorder with or without hyperkinetic movements and seizures, autosomal dominant', 'autosomal dominant intellectual disability 8', 'intellectual disability, autosomal dominant 8, formerly', 'GRIN1 autosomal dominant non-syndromic intellectual disability', 'autosomal dominant non-syndromic intellectual disability caused by mutation in GRIN1', 'NDHMSD']",0070038,614254,,C3280282,,,,,,,,
mondo:0013656,"intellectual disability, autosomal dominant 9","['autosomal dominant non-syndromic intellectual disability 9', 'intellectual disability, autosomal dominant 9', 'autosomal dominant mental retardation 9', 'intellectual disability, autosomal dominant type 9', 'MRD9', 'KIF1A autosomal dominant non-syndromic intellectual disability', 'mental retardation, autosomal dominant 9', 'autosomal dominant non-syndromic intellectual disability caused by mutation in KIF1A', 'autosomal dominant intellectual disability 9', 'mental retardation, autosomal dominant type 9', 'NESCAV syndrome']",0070039,614255,,C3280283,,C133742,,,,,,
mondo:0013657,"intellectual disability, autosomal dominant 10","['mental retardation, autosomal dominant type 10', 'intellectual disability, autosomal dominant 10', 'CACNG2 autosomal dominant non-syndromic intellectual disability', 'autosomal dominant non-syndromic intellectual disability caused by mutation in CACNG2', 'MRD10', 'mental retardation, autosomal dominant 10', 'intellectual disability, autosomal dominant type 10', 'autosomal dominant non-syndromic intellectual disability 10', 'autosomal dominant intellectual disability 10', 'autosomal dominant mental retardation 10']",0070040,614256,,C3280284,,,,,,,,
mondo:0013658,"intellectual disability, autosomal dominant 11","['autosomal dominant mental retardation 11', 'autosomal dominant non-syndromic intellectual disability caused by mutation in EPB41L1', 'intellectual disability, autosomal dominant 11', 'mental retardation, autosomal dominant type 11', 'MRD11', 'autosomal dominant intellectual disability 11', 'EPB41L1 autosomal dominant non-syndromic intellectual disability', 'intellectual disability, autosomal dominant type 11', 'autosomal dominant non-syndromic intellectual disability 11', 'mental retardation, autosomal dominant 11', 'intellectual developmental disorder, autosomal dominant 11']",0070041,614257,,C3280285,,,,,,,,
mondo:0013659,microcephaly-capillary malformation syndrome,"['MICCAP', 'MIC-CAP syndrome', 'microcephaly-capillary malformation syndrome', 'microcephaly-cutaneous capillary malformation syndrome', 'MIC-CM syndrome']",,614261,294016,C3280296,"['0.03262', '0.1881', '0.376', '-0.05054', '0.2793', '-0.2322', '0.1285', '0.489', '-1.228', '-0.3196', '0.1621', '0.1785', '0.339', '0.4443', '0.623', '-0.2102', '0.635', '0.4473', '-0.3926', '-1.069', '-0.1621', '0.03632', '0.1871', '-0.1235', '0.4814', '0.05414', '-0.1812', '0.1813', '0.3086', '-0.178', '-0.2169', '-0.743', '0.643', '0.2522', '-0.1136', '0.809', '-0.4812', '0.000983', '-0.03117', '-0.2935', '0.06824', '0.2673', '-0.629', '-0.479', '0.2666', '-0.3228', '0.7324', '0.3467', '0.09515', '-0.3074', '0.0926', '-0.523', '-0.2496', '-0.1771', '-0.3901', '0.3904', '-0.9165', '0.6177', '-0.615', '0.4905', '0.186', '0.5273', '0.502', '0.25', '-0.2382', '-0.03296', '0.5884', '-0.296', '-1.305', '0.3176', '-0.696', '1.001', '0.2301', '-0.7314', '0.058', '0.1552', '0.4238', '-0.1714', '-0.266', '-0.05273', '-0.4373', '1.076', '-0.05154', '0.5645', '-0.02353', '-0.6587', '0.08655', '-0.249', '1.015', '0.4736', '0.1628', '0.1963', '-0.1449', '0.3547', '-0.4255', '0.2568', '0.8276', '-0.521', '0.6064', '-0.5894']",,,,759.89,,,
mondo:0013660,"arthrogryposis, Perthes disease, and upward gaze palsy","['APUG', 'arthrogryposis, Perthes disease, and upward gaze palsy']",,614262,,C3280309,"['-0.0633', '0.1148', '0.0914', '-0.02977', '0.0454', '-0.1466', '0.00454', '0.1437', '-0.1255', '-0.0672', '-0.003004', '-0.03256', '0.004185', '-0.01929', '-0.04022', '-0.0487', '0.006508', '-0.11206', '-0.04214', '-0.2028', '0.05798', '-0.05124', '0.04767', '0.02292', '0.01976', '-0.05362', '0.01608', '0.05096', '0.006653', '0.01281', '0.03397', '0.0482', '0.1564', '0.06934', '0.04733', '-0.011925', '-0.0086', '-0.04153', '-0.03497', '-0.09106', '0.000609', '-0.1268', '-0.02693', '0.02017', '-0.00787', '-0.0685', '-0.006546', '0.1175', '0.07336', '0.006042', '-0.01875', '0.0355', '-0.03552', '-0.02994', '-0.02557', '-0.10675', '0.06067', '-0.0863', '-0.0975', '0.02888', '0.0547', '0.03177', '0.008545', '0.074', '-0.04556', '8.46e-05', '0.1367', '0.0741', '-0.07806', '0.1132', '-0.06866', '0.04758', '0.01723', '-0.0977', '0.04153', '0.092', '0.0575', '-0.003944', '-0.1392', '-0.1014', '0.007423', '-0.0776', '0.03262', '0.1481', '-0.04822', '-0.00392', '-0.06027', '0.0621', '0.06573', '0.002308', '0.0835', '0.0164', '0.05423', '0.0547', '0.1835', '0.04785', '0.1032', '-0.07465', '0.04114', '0.10516']",,,,,,,
mondo:0013661,combined malonic and methylmalonic acidemia,"['CMAMMA', 'combined malonic and methylmalonic aciduria']",0111263,614265,289504,C3280314,"['-0.2097', '0.261', '0.010376', '-0.239', '-0.03058', '-0.277', '-0.1592', '0.3237', '-0.1862', '0.2527', '-0.2788', '-0.2369', '0.0524', '-0.2151', '-0.1809', '-0.3665', '0.08655', '-0.262', '-0.3074', '-0.411', '0.03827', '-0.4592', '0.06537', '0.01072', '0.1761', '-0.1226', '0.05145', '-0.312', '-0.417', '-0.08466', '-0.03577', '0.1521', '0.3733', '0.204', '-0.1317', '0.0512', '-0.1848', '-0.2057', '-0.2397', '-0.2393', '-0.02434', '-0.493', '0.081', '-0.08777', '-0.4084', '-0.2069', '-0.0168', '-0.014114', '-0.3691', '0.406', '-0.2185', '0.02914', '0.13', '-0.1824', '-0.02083', '-0.08563', '0.3457', '-0.3376', '-0.286', '0.1534', '0.1138', '0.1418', '0.3286', '-0.2703', '0.0836', '0.1027', '0.3135', '0.1304', '-0.357', '0.0404', '0.0947', '0.12085', '-0.1583', '-0.1493', '0.04993', '0.08325', '0.03412', '-0.3909', '-0.06155', '0.02495', '0.3777', '-0.05154', '-0.1116', '0.2306', '0.4944', '0.0996', '-0.1804', '0.0944', '0.5396', '0.1742', '0.5054', '0.2847', '-0.0883', '0.0984', '0.2439', '0.4827', '0.2268', '-0.242', '-0.127', '0.1794']",,,C580002,,,,
mondo:0013662,Barrett esophagus,"['Barrett^s esophagus', 'Barrett^s ulcer of esophagus', 'Barrett esophagus', 'Barrett^s ulcer of oesophagus', 'columnar epithelial-lined Lower oesophagus', 'BE', 'adenocarcinoma of oesophagus', 'Barrett^s esophagus with esophagitis', 'Barrett^s oesophagus', 'adenocarcinoma of esophagus', 'ulcerative esophagitis', 'Barretts syndrome', 'columnar-lined oesophagus', 'cello', 'CLE', 'Barrett esophagus/esophageal adenocarcinoma', 'Barrett^s oesophagus with esophagitis', 'Barrett metaplasia', 'columnar-lined esophagus', 'columnar epithelial-lined Lower esophagus']",9206,614266,99976,C0279628,"['-0.1415', '-0.2369', '-0.01822', '0.2285', '0.2192', '-0.0475', '0.1616', '0.4866', '-0.5786', '0.02852', '0.3857', '-0.3425', '-0.5703', '0.2261', '-0.7764', '-0.817', '-0.08215', '0.05118', '0.1687', '-0.1842', '-0.0814', '-0.0877', '-0.1326', '-0.562', '0.2795', '-0.246', '0.4382', '0.4133', '-0.2063', '-0.192', '0.6816', '-0.5776', '0.5664', '-0.537', '0.9414', '0.267', '-0.3472', '0.2766', '0.315', '-0.3486', '0.1685', '-0.5195', '-0.0196', '-0.2883', '0.0451', '0.11035', '-0.1671', '-0.008064', '0.1573', '0.1904', '-0.0356', '-0.09534', '0.2698', '-0.548', '-0.08203', '0.592', '-0.55', '0.537', '-0.509', '-0.2155', '0.2161', '0.739', '0.5073', '-0.2625', '0.26', '-0.1743', '0.5903', '0.08374', '-0.2444', '0.6753', '0.158', '0.3967', '-0.832', '-0.2357', '0.426', '0.1169', '-0.3918', '0.1602', '0.191', '-0.1934', '0.1582', '-0.1008', '-0.003332', '-0.2089', '0.521', '-0.4875', '0.2073', '0.2067', '0.4666', '-0.2979', '-0.01373', '-0.0725', '-0.01437', '0.6343', '1.059', '-0.1515', '-0.3848', '-0.5747', '-0.8994', '0.007317']",C2891,0000280,D001471,530.85,,,
mondo:0013663,platelet-activating factor acetylhydrolase deficiency,"['platelet-activating factor acetylhydrolase deficiency (disease)', 'platelet-activating factor acetylhydrolase deficiency', 'PAFAD']",,614278,,C3280315,,,,C566640,,,,0040175
mondo:0013664,"46,XY disorder of sex development due to testicular 17,20-desmolase deficiency","['46,XY sex reversal type 8', '46,XY sex reversal 8', 'SRXY8', '46XY sex reversal 8', 'male pseudohermaphroditism due to deficiency of testicular 17,20-desmolase', '46XY sex reversal 8, modifier of']",0111773,614279,443087,C1839840,,,,C564109,,,,
mondo:0013665,"epilepsy, juvenile myoclonic, susceptibility to, 9","['EJM9', 'epilepsy, juvenile myoclonic, susceptibility to, 9']",0111328,614280,,,,,,,,,,
mondo:0013666,"Stickler syndrome, type 5","['COL9A2 autosomal recessive Stickler syndrome', 'STL5', 'STICKLER syndrome, type V', 'autosomal recessive Stickler syndrome caused by mutation in COL9A2']",,614284,,C3280342,,,,,,,,
mondo:0013668,tetrasomy 18p,"['tetrasomy type 18P', 'Isochromosome 18P syndrome', 'Isochromosome 18p', 'chromosome 18p tetrasomy', 'tetrasomy 18p', 'tetrasomy type 18p', 'tetrasomy chromosome 18p']",,614290,3307,C0795868,,,,C538306,758.89,,,
mondo:0013669,"breast-ovarian cancer, familial, susceptibility to, 4","['breast-ovarian cancer, familial, susceptibility to, type 4', 'breast-ovarian cancer, familial, susceptibility to, 4', 'BROVCA4', 'RAD51D hereditary breast ovarian cancer syndrome', 'susceptibility to familial breast-ovarian cancer 4', 'hereditary breast ovarian cancer syndrome caused by mutation in RAD51D']",,614291,,,,,,,,,,
mondo:0013670,"myopia, high, with cataract and vitreoretinal degeneration","['myopia, high, with cataract and vitreoretinal degeneration', 'MCVD']",,614292,,C3280346,,,,,,,,
mondo:0013671,"hydatidiform mole, recurrent, 2","['hydatidiform mole, recurrent, 2', 'HYDM2', 'KHDC3L complete hydatidiform mole', 'complete hydatidiform mole caused by mutation in KHDC3L', 'hydatidiform Mole, recurrent, type 2', 'hydatidiform Mole, complete', 'hydatidiform MOLE, recurrent, 2']",,614293,,C3280352,,,,,,,,
mondo:0013672,chromosome 15q25 deletion syndrome,['chromosome 15q25 deletion syndrome'],0060396,614294,,C3280355,,,,,,,,
mondo:0013673,Wolfram-like syndrome,"['Wolfram-like syndrome, autosomal dominant', 'WFSL', 'hearing loss, progressive, with optic atrophy and/or impaired glucose Regulation']",0080584,614296,411590,C4518338,"['-0.0441', '0.3384', '0.01878', '-0.003744', '-0.18', '-0.447', '-0.0713', '0.6', '-0.165', '-0.2224', '-0.2327', '-0.4968', '-0.02776', '-0.1765', '-0.00425', '-0.2006', '0.0687', '-0.0347', '-0.2695', '-0.2335', '0.1979', '-0.3367', '0.09033', '-0.0572', '0.3127', '0.3948', '-0.3447', '-0.5337', '0.1107', '-0.0944', '0.4233', '0.0917', '0.3604', '-0.02759', '0.1172', '-0.1824', '-0.005356', '-0.4175', '0.02124', '0.1752', '0.426', '-0.1876', '0.334', '0.1747', '0.2998', '-0.1722', '0.09705', '0.1625', '-0.1462', '0.001083', '0.11945', '0.859', '-0.079', '-0.01866', '0.1632', '0.2222', '0.208', '-0.414', '-0.3398', '0.0949', '0.3123', '0.1364', '0.228', '-0.2734', '-0.606', '0.364', '-0.1787', '0.425', '-0.4607', '0.4492', '-0.2751', '-0.3494', '0.03308', '0.06305', '0.3174', '0.02618', '0.3132', '0.1875', '-0.3887', '0.1727', '0.5093', '-0.2688', '0.0647', '0.4888', '0.0777', '0.1189', '0.3223', '0.529', '0.445', '0.4678', '0.292', '0.3672', '0.4465', '0.0763', '0.349', '-0.0784', '0.11993', '-0.354', '-0.1188', '0.3997']",,0009063,C565631,,,,
mondo:0013674,neurodegeneration with brain iron accumulation 4,"['C19orf12 neurodegeneration with brain iron accumulation', 'NBIA due to C19orf12 mutation', 'mitochondrial membrane protein-associated neurodegeneration', 'MPAN', 'neurodegeneration with brain iron accumulation type 4', 'neurodegeneration with brain iron accumulation caused by mutation in C19orf12', 'mitochondrial Protein-associated neurodegeneration', 'NBIA4', 'neurodegeneration with brain iron accumulation due to C19orf12 mutation', 'neurodegeneration with brain iron accumulation 4']",0110738,614298,289560,C3280371,"['-0.3657', '0.2715', '0.5107', '-0.4219', '-0.07526', '-0.451', '-0.1663', '1.174', '-0.5015', '0.1503', '-0.3457', '-0.4404', '-0.2463', '-0.3447', '0.2256', '-0.05692', '-0.1804', '-0.445', '-0.9023', '-0.5073', '-0.35', '-0.684', '-0.311', '0.8804', '-0.554', '-0.00287', '0.06714', '-0.1406', '-0.558', '0.1807', '0.3723', '-0.0722', '0.3623', '-0.6255', '0.04205', '0.0248', '-0.1602', '-0.2795', '0.1962', '0.103', '0.3652', '-0.1556', '0.4026', '0.4827', '0.677', '-0.3723', '-0.5073', '-0.1837', '0.2783', '-0.382', '-0.1433', '0.3577', '-0.677', '-0.328', '0.0815', '-0.1719', '0.4082', '0.1272', '-0.5283', '-0.298', '0.222', '0.3513', '0.674', '-0.3113', '-1.029', '0.2247', '0.627', '0.3147', '-0.2056', '0.401', '-0.497', '-0.6157', '-0.835', '0.1718', '0.625', '0.1982', '0.0873', '-0.1976', '-0.689', '-0.3816', '0.1439', '-0.6284', '0.1813', '0.6753', '0.2013', '0.1154', '0.3967', '0.56', '0.2742', '-0.05743', '0.3289', '0.3198', '-0.401', '0.1401', '0.433', '0.1185', '0.4502', '0.1068', '0.10266', '-0.255']",C175707,,,333.0,,,
mondo:0013675,multiple mitochondrial dysfunctions syndrome 2,"['multiple mitochondrial dysfunctions syndrome 2', 'MMDS2', 'multiple mitochondrial dysfunctions syndrome 2 with hyperglycinemia', 'BOLA3 deficiency', 'multiple mitochondrial dysfunctions syndrome type 2', 'fatal multiple mitochondrial dysfunctions syndrome caused by mutation in BOLA3', 'BOLA3 fatal multiple mitochondrial dysfunctions syndrome']",0080134,614299,401874,C3280378,"['-0.3667', '0.2382', '-0.2483', '0.02768', '-0.1008', '-0.4329', '-0.1515', '0.3103', '-0.64', '0.12103', '-0.2866', '-0.2133', '-0.08716', '-0.2788', '0.1471', '-0.2316', '-0.08746', '-0.02719', '-0.2406', '-0.546', '0.3032', '-0.2742', '0.3445', '-0.2042', '0.2146', '-0.1902', '-0.1504', '0.2338', '-0.08185', '0.1112', '0.2042', '0.293', '0.498', '0.3157', '0.05057', '-0.03293', '-0.1803', '-0.10846', '-0.10736', '0.02695', '0.10956', '-0.2876', '0.0579', '0.2646', '-0.1638', '-0.2964', '-0.10455', '0.1906', '0.0258', '-0.04547', '-0.0625', '0.0462', '-0.04095', '-0.1888', '-0.06384', '-0.2164', '0.2747', '-0.095', '-0.001385', '0.4111', '0.0741', '0.02217', '0.5386', '-0.1351', '-0.494', '0.0901', '0.4548', '0.3752', '-0.3083', '0.3894', '-0.237', '0.2118', '-0.1236', '-0.0834', '-0.04398', '-0.1741', '0.07544', '0.2015', '-0.2257', '-0.02948', '0.03693', '0.004524', '-0.0636', '0.2134', '-0.006847', '-0.06793', '0.3088', '0.3538', '0.3774', '0.3555', '0.3235', '0.3098', '0.10596', '-0.006886', '0.2479', '0.4033', '0.4077', '-0.05527', '0.24', '-0.132']",,,,,,,
mondo:0013677,"Emery-Dreifuss muscular dystrophy 7, autosomal dominant","['Ehlers-Danlos syndrome, classic-like, 1', 'Emery-Dreifuss muscular dystrophy 7, autosomal dominant', 'EDMD7', 'autosomal dominant Emery-Dreifuss muscular dystrophy caused by mutation in TMEM43', 'TMEM43 autosomal dominant Emery-Dreifuss muscular dystrophy', 'EMERY-Dreifuss muscular dystrophy 7, autosomal dominant']",0070252,614302,,C3553060,,,,,,,,
mondo:0013678,EDICT syndrome,"['autosomal dominant keratoconus with early-onset anterior polar cataracts', 'familial keratoconus with cataract', 'keratoconus, familial, with early-onset anterior polar cataract', 'EDICT syndrome', 'endothelial dystrophy, iris hypoplasia, congenital cataract, and stromal thinning syndrome', 'keratoconus with cataract', 'KTCNCT', 'EDICT', 'endothelial dystrophy-iris hypoplasia-congenital cataract-stromal thinning syndrome']",,614303,293936,C3280392,,,,,,,,
mondo:0013679,sclerosteosis 2,"['LRP4 sclerosteosis', 'sclerosteosis 2', 'sclerosteosis caused by mutation in LRP4', 'sclerosteosis type 2', 'SOST2']",0060757,614305,,C3280402,,,,,,,,
mondo:0013680,cognitive impairment with or without cerebellar ataxia,"['CIAT', 'cognitive impairment with or without cerebellar ataxia']",,614306,,C3280415,"['-0.06683', '0.04294', '-0.06058', '-0.04318', '-0.01738', '-0.1285', '0.0348', '0.1758', '-0.1738', '-0.05078', '-0.05035', '-0.06256', '-0.05728', '0.02652', '0.0687', '-0.147', '0.0027', '-0.12335', '-0.0627', '-0.2305', '0.012505', '-0.011475', '0.004124', '-0.0678', '0.06586', '-0.063', '0.000989', '-0.03683', '-0.01645', '-0.03293', '0.05643', '-0.01857', '0.1425', '0.002005', '0.01575', '-0.04227', '-0.1071', '-0.04883', '-0.10406', '-0.0984', '0.07007', '-0.1461', '0.05264', '0.02364', '0.00936', '-0.154', '-0.0365', '0.08844', '-0.0371', '0.02913', '-0.004364', '0.08813', '-0.02977', '-0.005905', '0.01318', '0.02695', '0.1399', '-0.0873', '-0.1929', '0.0147', '0.0335', '0.10345', '0.02452', '0.06287', '-0.1174', '-0.00787', '0.09174', '0.10443', '-0.04044', '0.1558', '-0.0646', '0.1039', '0.02888', '-0.1631', '0.0489', '0.0357', '0.093', '-0.02779', '-0.04498', '-0.01936', '-0.04178', '-0.0568', '-0.04773', '0.10474', '-0.006413', '-0.003872', '-0.00209', '0.1285', '0.1638', '0.02911', '0.08185', '0.144', '-0.02092', '0.0238', '0.1873', '0.1136', '0.0919', '-0.0808', '0.02914', '0.1076']",,,,,,,
mondo:0013681,alpha-methylacyl-CoA racemase deficiency,"['AMACR deficiency', 'AMACR', 'alpha-methylacyl-CoA racemase deficiency', 'AMACRD']",0060602,614307,,C3280428,"['-0.2463', '0.258', '0.1837', '-0.1114', '-0.1793', '-0.375', '-0.1687', '0.2666', '-0.4163', '0.1127', '-0.1843', '-0.003784', '-0.2517', '-0.0983', '0.1393', '-0.238', '0.0127', '-0.32', '-0.1903', '-0.474', '0.12317', '-0.307', '-0.003386', '0.02242', '0.2037', '-0.0822', '0.0596', '0.07245', '-0.0662', '-0.1526', '0.1132', '0.03357', '0.3987', '-0.02629', '-0.0641', '-0.152', '-0.1924', '-0.175', '0.08356', '-0.1892', '0.03638', '-0.3765', '0.1725', '0.3086', '-0.0672', '-0.2008', '-0.04688', '0.07904', '0.03284', '0.1423', '-0.1064', '0.4763', '-0.17', '0.1268', '0.2225', '-0.1543', '0.5723', '-0.04846', '-0.311', '0.2263', '-0.01463', '0.07086', '0.4412', '-0.02649', '-0.0523', '0.3298', '0.2063', '0.2698', '-0.1432', '0.134', '-0.421', '0.1562', '0.064', '0.328', '0.3035', '-0.005573', '0.263', '0.2137', '0.03314', '-0.10223', '0.0434', '-0.3806', '-0.0636', '0.2046', '0.3025', '-0.1346', '0.2505', '0.2722', '0.3735', '0.2042', '0.1708', '0.291', '-0.03653', '-0.04517', '0.2325', '0.4136', '0.2485', '-0.1873', '0.23', '-0.02216']",C119677,1001980,C565768,,,,
mondo:0013682,vesicoureteral reflux 4,"['vesicoureteral reflux 4', 'VUR4']",,614317,,C3280439,,,,,,,,
mondo:0013683,vesicoureteral reflux 5,"['VUR5', 'vesicoureteral reflux 5']",,614318,,C3280440,,,,,,,,
mondo:0013684,vesicoureteral reflux 6,"['vesicoureteral reflux 6', 'VUR6']",,614319,,C3280441,,,,,,,,
mondo:0013685,"pancreatic cancer, susceptibility to, 4","['PNCA4', 'pancreatic cancer, susceptibility to, 4', 'susceptibility to pancreatic cancer 4', 'BRCA1 familial pancreatic carcinoma', 'pancreatic cancer, susceptibility to, type 4', 'familial pancreatic carcinoma caused by mutation in BRCA1']",,614320,,,,,,,,,,
mondo:0013686,"distal myopathy, Tateyama type","['myopathy, distal, Tateyama type', 'MPDT']",0111191,614321,488650,C3280443,,,,,,,,
mondo:0013687,autosomal recessive spinocerebellar ataxia 12,"['spinocerebellar ataxia, autosomal recessive 12', 'spinocerebellar ataxia with intellectual disability and epilepsy', 'spinocerebellar ataxia with mental retardation and epilepsy', 'autosomal recessive spinocerebellar ataxia type 12', 'spinocerebellar ataxia, autosomal recessive type 12', 'WWOX autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome', 'SCAR12', 'autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in WWOX', 'autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to WWOX deficiency', 'WWOX autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome']",0080060,614322,284282,C3280452,"['-0.1133', '-0.2827', '0.1594', '0.015', '-0.1164', '-0.9375', '0.11127', '0.09796', '-0.586', '-0.802', '0.1667', '0.3257', '-0.1924', '0.11646', '0.4565', '-0.267', '-0.1951', '-0.1787', '0.04065', '-0.8965', '-0.1271', '-0.346', '0.1974', '-0.4768', '0.594', '-0.6', '-0.251', '0.261', '-0.224', '-0.7817', '0.04993', '0.4624', '-0.5635', '-0.2041', '0.4023', '-0.0695', '-0.284', '0.1661', '0.574', '0.31', '0.4067', '0.1178', '-0.657', '0.638', '0.361', '-0.664', '0.0862', '0.3926', '0.3381', '0.03247', '-0.197', '0.306', '-0.0872', '-0.3154', '-0.1068', '-0.8325', '0.2754', '0.6074', '-0.1249', '0.577', '-0.764', '0.1693', '0.459', '-0.1747', '-0.4412', '0.673', '0.194', '0.5435', '-0.578', '0.3733', '0.7866', '0.7188', '-0.0655', '-0.6426', '0.6064', '0.2588', '0.3328', '0.2805', '0.2252', '0.5215', '-0.5425', '-0.82', '0.2878', '0.813', '-0.2363', '-0.722', '0.1603', '-0.0595', '0.4731', '0.5015', '0.5645', '0.3708', '0.0572', '0.0894', '0.99', '1.057', '0.4036', '0.3645', '-0.442', '0.0746']",,,,,,,
mondo:0013688,linear and whorled nevoid hypermelanosis,"['melanosis Neviformis', 'nevoid hypermelanosis, linear and whorled', 'zosteriform lentiginous nevus', 'zosteriform hyperpigmentation', 'Becker^s Nevus', 'hyperpigmentation, progressive cribriform and zosteriform', 'progressive cribriform and zosteriform hyperpigmentation', 'Becker Nevus', 'linear and whorled hypermelanosis', 'pigmented hairy Epidermal Nevus', 'reticulate hyperpigmentation of Iijima', 'pigmented hairy Nevus of Becker', 'LWNH', 'linear papular ectodermal-mesodermal hamartoma', 'zebra-like hyperpigmentation']",,614323,79150,C1304501,,C3924,,,,,,
mondo:0013689,ovarian dysgenesis 3,"['ODG3', '46 XX gonadal dysgenesis caused by mutation in PSMC3IP', 'ovarian dysgenesis type 3', 'ovarian dysgenesis 3', 'PSMC3IP 46 XX gonadal dysgenesis']",0080495,614324,,C3280471,,,,,,,,
mondo:0013690,Pitt-Hopkins-like syndrome 2,"['Pitt-Hopkins-like syndrome type 2', 'Pitt-Hopkins-like syndrome 2', 'PTHSL2', 'Pitt-Hopkins-like syndrome caused by mutation in NRXN1', 'NRXN1 Pitt-Hopkins-like syndrome']",0111332,614325,,C3280479,,,,,,,,
mondo:0013691,Feingold syndrome type 2,"['Feingold syndrome type 2', 'brachydactyly-short stature-microcephaly syndrome', 'Feingold syndrome 2', 'FS2', 'microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 2', 'microcephaly-digital anomalies-normal intelligence syndrome type 2', 'MMT type 2', 'brachydactyly with short stature and microcephaly', 'FGLDS2', 'Brunner-Winter syndrome type 2']",,614326,391646,C3280489,"['0.4932', '-0.3633', '0.2742', '-0.3936', '-0.279', '0.2013', '0.4258', '0.692', '-0.5435', '-0.741', '0.09674', '-0.08887', '-0.3774', '0.437', '-0.3394', '0.05106', '0.11285', '-0.05273', '-0.09644', '-0.9844', '0.2052', '0.02025', '-0.1001', '0.2368', '-0.2842', '-0.1742', '-0.5977', '0.2524', '0.527', '-0.4182', '0.5796', '-0.3833', '0.415', '0.3972', '-0.02266', '-0.5864', '0.03308', '-0.364', '0.1664', '0.316', '0.2651', '-0.3733', '0.2893', '0.007248', '0.3674', '-0.005142', '-0.03925', '0.397', '-0.3538', '-0.01854', '-0.2026', '-0.05026', '-0.1803', '-0.573', '-0.6553', '-0.02614', '-0.454', '0.1053', '-0.2078', '0.3696', '0.3525', '0.521', '0.3096', '0.4192', '-0.2042', '-0.04135', '-0.4233', '-0.1769', '-0.566', '0.1393', '-0.515', '-0.233', '0.02226', '-0.353', '0.4795', '-0.2502', '0.00761', '-0.558', '-0.508', '-0.419', '-0.01306', '0.2883', '-0.03738', '0.3762', '-0.332', '0.6265', '-0.0387', '0.3997', '0.311', '0.4648', '0.1908', '0.434', '0.1326', '-0.03354', '0.5483', '0.10364', '0.11694', '-1.055', '0.706', '0.544']",,,,,,,
mondo:0013692,BAP1-related tumor predisposition syndrome,"['BAP1 tumour predisposition syndrome', 'tumor predisposition syndrome', 'tumor susceptibility linked to germline BAP1 mutations', 'tumour predisposition syndrome', 'TPDS', 'tumour susceptibility linked to germline BAP1 mutations', 'BAP1 tumor predisposition syndrome']",,614327,289539,C3280492,"['-0.01874', '0.221', '-0.285', '-0.2183', '0.3547', '-0.2795', '0.1035', '0.01548', '-0.3535', '-0.004513', '0.2893', '0.2883', '0.03763', '-0.1517', '-0.4944', '-0.2842', '-0.0163', '-0.2179', '0.3267', '-0.10004', '-0.1311', '-0.2666', '0.2878', '-0.249', '0.564', '-0.0308', '-0.1044', '0.1409', '-0.01802', '-0.1743', '0.6733', '-0.07294', '0.4766', '-0.2324', '0.149', '0.10455', '-0.6177', '-0.02477', '-0.00947', '-0.3716', '0.02396', '-0.4392', '0.1279', '-0.1816', '0.1029', '-0.1055', '-0.2578', '-0.00474', '0.3606', '-0.1677', '0.2107', '0.2096', '-0.589', '0.2607', '-0.4304', '-0.1216', '0.1937', '-0.0894', '-0.453', '-0.05154', '0.5776', '0.01451', '-0.274', '0.2546', '0.0282', '0.06287', '0.4543', '0.4023', '0.05737', '0.521', '0.03403', '-0.00973', '0.1443', '0.2303', '0.1764', '-0.04056', '-0.0714', '-0.07806', '0.03452', '-0.717', '-0.3833', '0.2927', '-0.2406', '-0.133', '-0.57', '-0.4565', '0.421', '0.1827', '0.1998', '-0.288', '0.01069', '0.3557', '-0.045', '-0.325', '0.5874', '0.1792', '0.4802', '-0.069', '-0.2158', '-0.1272']",,,,,,,
mondo:0013693,"inflammatory skin and bowel disease, neonatal, 1","['inflammatory skin and bowel disease, neonatal, type 1', 'NISBD1', 'inflammatory skin and bowel disease, neonatal, 1', 'neonatal inflammatory skin and bowel disease caused by mutation in ADAM17', 'ADAM17 neonatal inflammatory skin and bowel disease']",,614328,,C3280501,,,,,,,,
mondo:0013694,"intellectual disability, autosomal recessive 31","['MRT31', 'intellectual disability, autosomal recessive 31', 'mental retardation, autosomal recessive 31']",0081191,614329,,C3280523,,,,,,,,
mondo:0013695,"colorectal cancer, hereditary nonpolyposis, type 6","['HNPCC6', 'colorectal cancer, hereditary nonpolyposis, type 6', 'TGFBR2 hereditary nonpolyposis colon cancer', 'colon cancer, hereditary nonpolyposis, type 6', 'hereditary nonpolyposis colon cancer caused by mutation in TGFBR2']",0070273,614331,,C1860896,,,,C566039,,,,
mondo:0013696,chromosome 2p16.3 deletion syndrome,"['schizophrenia, susceptibility to, 17', 'chromosome 2P16.3 deletion syndrome']",,614332,,C3808494,,,,,,,,
mondo:0013697,"intellectual disability, autosomal recessive 29","['mental retardation, autosomal recessive 29', 'MRT29', 'intellectual disability, autosomal recessive 29']",0081192,614333,,C3280525,,,,,,,,
mondo:0013698,"arthrogryposis, distal, type 1B","['DA1B', 'arthrogryposis, distal, type 1B']",0111598,614335,,C3280526,,,,,,,,
mondo:0013699,Lynch syndrome 4,"['hereditary nonpolyposis colon cancer caused by mutation in PMS2', 'PMS2 hereditary nonpolyposis colon cancer', 'colorectal cancer, hereditary nonpolyposis, type 4', 'HNPCC4']",0070275,614337,,C1838333,,,,C563971,,,,
mondo:0013700,pancreatic triacylglycerol lipase deficiency,"['pancreatic colipase deficiency', 'pancreatic lipase deficiency', 'pancreatic triglyceride lipase deficiency', 'lipase, congenital absence of pancreatic', 'PNLIPD', 'PL deficiency', 'lipase and colipase, deficiency of', 'lipase and colipase, congenital absence of pancreatic', 'colipase, congenital absence of pancreatic']",,614338,309031,C0268240,"['-0.4175', '0.2198', '0.136', '-0.11145', '0.4297', '-0.11554', '-0.6157', '0.4119', '-0.02974', '-0.3206', '-0.2588', '0.042', '0.05014', '-0.1506', '-0.241', '-0.1932', '0.2786', '-0.0779', '-0.508', '-0.563', '0.08856', '-0.752', '0.5195', '0.1302', '0.3582', '-0.0636', '0.3533', '0.1958', '0.193', '-0.631', '0.3948', '0.0986', '0.2025', '0.1339', '-0.1873', '-0.15', '-0.2292', '-0.1161', '0.2274', '-0.169', '-0.3074', '-0.249', '0.2502', '0.033', '-0.465', '-0.8003', '0.3562', '-0.05353', '0.2642', '0.0832', '0.0455', '-0.02922', '-0.1611', '0.02898', '-0.0358', '-0.2966', '0.2542', '-0.3662', '-0.538', '0.2123', '0.2595', '0.3762', '0.128', '-0.555', '0.3816', '0.5146', '0.225', '0.1732', '-0.2905', '-0.335', '-0.2578', '-0.1324', '-0.0766', '0.1632', '0.4531', '0.1144', '0.1758', '0.04633', '-0.0411', '0.2495', '-0.0682', '0.00859', '0.1666', '0.0905', '-0.01211', '0.05533', '0.03836', '0.002851', '0.687', '0.04272', '0.3423', '0.488', '-0.1819', '-0.3704', '0.4841', '0.1616', '0.07245', '-0.574', '-0.3062', '0.3577']",C129030,,,277.89,K90.3,,
mondo:0013702,"intellectual disability, autosomal recessive 27","['intellectual developmental disorder, autosomal recessive 27', 'LINS1 autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive 27', 'intellectual disability, autosomal recessive 27', 'autosomal recessive non-syndromic intellectual disability caused by mutation in LINS1', 'intellectual disability, autosomal recessive type 27', 'mental retardation, autosomal recessive type 27', 'MRT27']",0081193,614340,,C3280538,,,,,,,,
mondo:0013703,"intellectual disability, autosomal recessive 33","['MRT33', 'mental retardation, autosomal recessive 33', 'intellectual disability, autosomal recessive 33']",0081194,614341,,C3280539,,,,,,,,
mondo:0013704,"intellectual disability, autosomal recessive 30","['intellectual disability, autosomal recessive 30', 'mental retardation, autosomal recessive 30', 'MRT30']",0081195,614342,,C3280540,,,,,,,,
mondo:0013705,"intellectual disability, autosomal recessive 19","['mental retardation, autosomal recessive 19', 'MRT19', 'intellectual disability, autosomal recessive 19']",,614343,,C3280541,,,,,,,,
mondo:0013706,"intellectual disability, autosomal recessive 23","['MRT23', 'mental retardation, autosomal recessive 23', 'intellectual disability, autosomal recessive 23']",0081196,614344,,C3280542,,,,,,,,
mondo:0013707,"intellectual disability, autosomal recessive 24","['intellectual disability, autosomal recessive 24', 'mental retardation, autosomal recessive 24', 'MRT24']",0081197,614345,,C3280543,,,,,,,,
mondo:0013708,"intellectual disability, autosomal recessive 25","['intellectual disability, autosomal recessive 25', 'mental retardation, autosomal recessive 25', 'MRT25']",0081198,614346,,C3280544,,,,,,,,
mondo:0013709,"intellectual disability, autosomal recessive 28","['mental retardation, autosomal recessive 28', 'MRT28', 'intellectual disability, autosomal recessive 28']",0081199,614347,,C3280545,,,,,,,,
mondo:0013710,Lynch syndrome 5,"['hereditary nonpolyposis colon cancer caused by mutation in MSH6', 'colorectal cancer, hereditary nonpolyposis, type 5', 'HNPCC5', 'MSH6 hereditary nonpolyposis colon cancer']",0070272,614350,,C1833477,,,,C563456,,,,
mondo:0013711,peripheral neuropathy-myopathy-hoarseness-hearing loss syndrome,"['PNMHH', 'peripheral neuropathy, myopathy, hoarseness, and hearing loss', 'peripheral neuropathy-myopathy-hoarseness-deafness syndrome']",,614369,397744,C3280556,"['0.4995', '0.5684', '-0.3555', '0.7915', '-0.1035', '-0.04218', '-0.2502', '-0.1106', '-0.0572', '0.2375', '0.2515', '-0.2289', '0.2249', '0.3652', '-0.3064', '-0.000671', '-0.1211', '0.2817', '-0.5776', '-0.3774', '0.3896', '-0.4224', '-0.05005', '0.289', '0.007164', '0.09784', '-0.2957', '-0.1755', '0.05112', '-1.034', '0.4421', '0.02507', '0.09204', '-0.4204', '0.1144', '-0.325', '-0.4731', '-0.361', '0.2634', '-0.602', '-0.6177', '-0.524', '-0.1638', '0.3215', '0.0598', '-0.6514', '0.3857', '0.1862', '0.5356', '0.2922', '-0.456', '0.3193', '0.2576', '0.322', '-0.06125', '-0.437', '0.0782', '-0.42', '-0.7524', '-0.5195', '-0.497', '0.1729', '-0.12006', '0.694', '-0.3481', '0.559', '0.3508', '1.05', '-0.1655', '0.3074', '-0.2108', '0.2861', '-0.1989', '-1.113', '0.951', '0.3232', '-0.05334', '0.6187', '0.1794', '0.1805', '-0.4248', '-0.4456', '-0.2324', '0.138', '-0.04034', '-0.04166', '0.2493', '0.308', '0.5356', '-0.0192', '0.0719', '-0.0633', '-0.1448', '0.0886', '-0.1442', '0.0306', '-0.4724', '-0.00434', '-0.00686', '-0.123']",,,,,,,
mondo:0013712,"surfactant metabolism dysfunction, pulmonary, 5","['pulmonary alveolar proteinosis 5', 'Pap due to Csf2Rb deficiency', 'hereditary pulmonary alveolar proteinosis caused by mutation in CSF2RB', 'surfactant metabolism dysfunction, pulmonary, 5', 'surfactant metabolism dysfunction, pulmonary, type 5', 'CSF2RB hereditary pulmonary alveolar proteinosis', 'Csf2Rb deficiency', 'SMDP5']",,614370,,C3280574,,,,,,,,
mondo:0013713,"dengue virus, susceptibility to","['susceptibility to dengue virus', 'Dengue hemorrhagic fever, susceptibility to', 'dengue virus, susceptibility to', 'Dengue fever, protection against', 'Dengue fever, susceptibility to', 'Dengue shock syndrome, susceptibility to']",,614371,99828,,"['-0.01182', '0.02104', '0.0101', '-0.0091', '0.00537', '-0.0437', '0.03903', '0.02342', '-0.01718', '-0.0212', '-0.00965', '0.00934', '0.00569', '0.002243', '-0.01595', '-0.01463', '-0.00981', '-0.01477', '-0.02486', '-0.04324', '0.01921', '-0.02895', '0.03036', '-0.014694', '-0.01064', '0.00246', '-0.011215', '-0.0003207', '-0.01607', '-0.0334', '0.0191', '-0.01481', '0.0473', '0.004883', '0.01616', '-0.015434', '-0.02145', '-0.011894', '-0.00665', '-0.02246', '0.00813', '-0.007256', '0.02478', '-0.0186', '0.006023', '-0.03168', '-0.00796', '0.02814', '0.01126', '0.00778', '-0.0301', '-0.009346', '0.01671', '0.014755', '-0.02661', '0.004883', '0.02342', '-0.02182', '-0.03076', '-0.0083', '0.01804', '0.0406', '-0.00582', '0.00646', '0.01207', '0.008545', '0.03732', '0.02959', '-0.02411', '0.0687', '-0.02019', '0.003057', '0.01248', '-0.03683', '0.01761', '0.02528', '0.004612', '0.001339', '0.003725', '-0.00814', '-0.03015', '5.966e-05', '-0.00774', '0.03955', '-0.01162', '0.007217', '0.03192', '0.01973', '0.04758', '0.006016', '0.02132', '0.011566', '-0.00629', '0.01021', '0.0609', '0.04785', '0.02657', '-0.0501', '-0.003033', '0.003696']",,,,,,,
mondo:0013714,mannose-binding lectin deficiency,"['MBP deficiency', 'MBL2 deficiency', 'MBLD', 'mannose-binding protein deficiency', 'lectin complement activation pathway, defect in, 1', 'MBL deficiency', 'mannose-binding lectin deficiency']",,614372,,C3280586,,,,C563602,279.19,,,
mondo:0013715,amyotrophic lateral sclerosis type 16,"['SIGMAR1 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis 16, juvenile', 'ALS16', 'amyotrophic lateral sclerosis caused by mutation in SIGMAR1', 'amyotrophic lateral sclerosis 16']",0060207,614373,,C3280587,,,,,,,,
mondo:0013716,"aortic aneurysm, familial abdominal, 4","['AAA4', 'aortic aneurysm, familial abdominal, 4']",,614375,,C3280597,,,,,,,,
mondo:0013717,asphyxiating thoracic dystrophy 5,"['Jeune syndrome caused by mutation in WDR19', 'asphyxiating thoracic dystrophy type 5', 'WDR19 Jeune syndrome', 'short-rib thoracic dysplasia 5 with or without polydactyly', 'ATD5', 'asphyxiating thoracic dystrophy 5', 'SRTD5']",0110089,614376,,C3280598,,,,,,,,
mondo:0013718,nephronophthisis 13,"['NPHP13', 'nephronophthisis type 13', 'nephronophthisis 13']",0111121,614377,,C3280612,,,,,,,,
mondo:0013719,cranioectodermal dysplasia 4,"['CED4', 'cranioectodermal dysplasia 4', 'cranioectodermal dysplasia type 4']",0080806,614378,,C3280616,,,,,,,,
mondo:0013720,complement component 4b deficiency,"['complement component 4b deficiency', 'C4B deficiency', 'complement component 4B deficiency', 'C4BD', 'classic complement early component deficiency caused by mutation in C4B', 'C4B classic complement early component deficiency']",0060298,614379,,C3280641,,,,,,,,
mondo:0013721,complement component 4a deficiency,"['C4A classic complement early component deficiency', 'complement component 4a deficiency', 'classic complement early component deficiency caused by mutation in C4A', 'complement component 4A deficiency', 'C4AD', 'C4A deficiency']",0060297,614380,,C3280642,,,,C565167,,,,
mondo:0013722,hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism,"['HLD8', 'leukodystrophy, hypomyelinating, 8, with or without oligodontia and/or hypogonadotropic hypogonadism', 'cerebellar hypoplasia with endosteal sclerosis', 'leukodystrophy caused by mutation in POLR3B', 'endosteal sclerosis-cerebellar hypoplasia syndrome', 'POLR3B leukodystrophy']",0060797,614381,85186,C3280644,,,,C535353,,,,
mondo:0013723,"bacteremia, susceptibility to, 1","['BACTS1', 'bacteremia, susceptibility to, type 1', 'TIRAP bacteremia, susceptibility', 'bacteremia, resistance to', 'bacteremia, susceptibility to, 1', 'bacteremia, susceptibility caused by mutation in TIRAP', 'bacteremia, protection against']",,614382,,,,,,,,,,
mondo:0013724,"bacteremia, susceptibility to, 2","['bacteremia, susceptibility to, type 2', 'CISH bacteremia, susceptibility', 'BACTS2', 'bacteremia, susceptibility caused by mutation in CISH', 'bacteremia, susceptibility to, 2', 'bacteremia, susceptibility to']",,614383,,,,,,,,,,
mondo:0013725,"colorectal cancer, hereditary nonpolyposis, type 7","['HNPCC7', 'MLH3 hereditary nonpolyposis colon cancer', 'colorectal cancer, hereditary nonpolyposis, type 7', 'hereditary nonpolyposis colon cancer caused by mutation in MLH3']",0070276,614385,,C1858380,,,,C565777,,,,
mondo:0013726,"encephalopathy, lethal, due to defective mitochondrial peroxisomal fission 1","['encephalopathy due to defective mitochondrial and peroxisomal fission 1', 'lethal encephalopathy due to mitochondrial and peroxisomal fission defect', 'DNM1L-associated encephalopathy due to peroxisomal and mitochondrial fission defect', 'EMPF1', 'encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission', 'EMPF']",0070347,614388,330050,C3280660,"['-0.2354', '0.1399', '0.01845', '-0.01717', '0.0195', '-0.2401', '-0.00836', '0.1693', '-0.1094', '-0.007805', '-0.07404', '-0.1013', '0.01306', '-0.0533', '-0.015465', '-0.0966', '0.004025', '-0.013054', '-0.1321', '-0.334', '-0.01901', '-0.11664', '0.2037', '-0.09625', '-0.04303', '-0.0605', '-0.07465', '-0.02898', '0.02571', '-0.1293', '0.0726', '0.1298', '0.282', '0.1292', '-0.00285', '-0.1643', '0.06018', '-0.1385', '-0.05222', '-0.1919', '0.02332', '-0.2213', '-0.00817', '-0.01377', '-0.161', '-0.1406', '-0.00909', '0.08997', '0.00924', '0.0752', '-0.0633', '-0.1222', '-0.001761', '-0.04828', '-0.1147', '-0.11505', '0.19', '-0.03943', '-0.1564', '0.1255', '0.11743', '0.0771', '0.1686', '0.01874', '-0.0379', '-0.03464', '0.2341', '0.09607', '-0.2424', '0.106', '-0.11444', '0.04837', '0.014725', '-0.0228', '-0.01894', '0.0434', '0.0898', '0.01991', '-0.10693', '0.0256', '-0.01611', '0.112', '-0.0942', '0.1414', '0.0558', '0.02354', '0.1132', '0.207', '0.2125', '-0.021', '0.1864', '0.06396', '-0.01002', '0.01086', '0.2676', '0.1731', '0.2512', '-0.2473', '0.05298', '0.03894']",,,,,,,
mondo:0013727,"pregnancy loss, recurrent, susceptibility to, 1","['pregnancy loss, recurrent, susceptibility caused by mutation in F5', 'Rpl', 'Rprgl', 'embryonic loss, recurrent', 'miscarriage, recurrent', 'foetal loss, recurrent, susceptibility to', 'RPRGL1', 'fetal loss, recurrent, susceptibility to', 'abortion, spontaneous, recurrent', 'stillbirth, recurrent', 'pregnancy loss, recurrent, susceptibility to, type 1', 'pregnancy loss, recurrent, susceptibility to, 1', 'F5 pregnancy loss, recurrent, susceptibility']",,614389,,,,,0008899,,,,,
mondo:0013728,"pregnancy loss, recurrent, susceptibility to, 2","['pregnancy loss, recurrent, susceptibility caused by mutation in F2', 'RPRGL2', 'F2 pregnancy loss, recurrent, susceptibility', 'pregnancy loss, recurrent, susceptibility to, 2', 'pregnancy loss, recurrent, susceptibility to, type 2']",,614390,,,,,,,,,,
mondo:0013729,"pregnancy loss, recurrent, susceptibility to, 3","['pregnancy loss, recurrent, susceptibility to, type 3', 'RPRGL3', 'pregnancy loss, recurrent, susceptibility caused by mutation in ANXA5', 'pregnancy loss, recurrent, susceptibility to, 3', 'ANXA5 pregnancy loss, recurrent, susceptibility']",,614391,,,,,,,,,,
mondo:0013730,graft versus host disease,"['graft-versus-host disease', 'graft vs host disease', 'graft versus host disease', 'GVH', 'graft-versus-host disease, resistance to', 'diseases, graft-vs-host', 'graft-versus-host diseases', 'graft-versus-host disease, susceptibility to', 'GVHD', 'runt disease', 'graft vs. host disease', 'disease, graft-versus-host', 'homologous wasting disease', 'disease, homologous wasting', 'disease, graft-vs-host', 'diseases, graft-versus-host', 'disease, runt', 'graft-vs-host disease', 'graft-VS-host diseases', 'graft-versus-host-disease']",0081267,,39812,C0018133,"['-0.0689', '0.1066', '0.01545', '-0.04395', '0.010155', '-0.0624', '0.01229', '0.06097', '-0.03137', '-0.01724', '-0.06537', '-0.04214', '-0.02084', '0.008644', '-0.03696', '-0.0824', '-0.01804', '-0.05304', '-0.01816', '-0.1761', '-0.00451', '-0.0932', '0.0781', '-0.05048', '0.05127', '-0.03433', '-0.02307', '0.00996', '-0.02165', '-0.0636', '0.0855', '0.00898', '0.10095', '0.006927', '0.03738', '-0.0498', '-0.02513', '-0.0557', '0.0163', '-0.0746', '-0.02379', '-0.0735', '0.0228', '-0.0412', '-0.01495', '-0.0414', '-0.04102', '-0.02107', '-0.01136', '0.05554', '-0.02324', '-0.01732', '0.02051', '0.02667', '-0.02287', '-0.01424', '0.0728', '-0.004112', '-0.1157', '0.03763', '0.0548', '0.06976', '-0.0369', '-0.01098', '0.03366', '-0.02385', '0.1149', '0.0649', '-0.0576', '0.109', '-0.0748', '-0.01372', '0.03165', '-0.0702', '0.02284', '0.00451', '0.00874', '-0.01158', '-0.05276', '-0.05347', '-0.03555', '-0.00757', '-0.00619', '0.05994', '-0.06885', '-0.008606', '0.03064', '0.07587', '0.1127', '0.01283', '0.04816', '0.04337', '-0.02873', '0.02184', '0.1727', '0.08856', '0.039', '-0.11346', '-0.04733', '0.02495']",C3063,,D006086,279.50,,10018651,
mondo:0013731,MEGF10-related myopathy,"['congenital myopathy 10A, severe variant', 'A congenital myopathy caused by mutations in the multiple epidermal growth factor-like domains 10 (MEGF10) gene, which causes early-onset myopathy characterized by severe weakness, scoliosis, joint contractures, areflexia, respiratory distress, and dysphagia, and a milder phenotype of minicore myopathy.', 'myopathy, areflexia, respiratory distress, and dysphagia, early-onset, mild variant', 'early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome', 'A congenital myopathy caused by mutations in the multiple epidermal growth factor-like domains 10 (MEGF10) gene, which causes early-onset myopathy characterised by severe weakness, scoliosis, joint contractures, areflexia, respiratory distress, and dysphagia, and a milder phenotype of minicore myopathy.', 'myopathy, areflexia, respiratory distress, and dysphagia, early-onset', 'EMARDD', 'early-onset myopathy, areflexia, respiratory distress and dysphagia', 'MEGF10 myopathy']",0111333,614399,439212,C3280679,,,,,,,,
mondo:0013732,"glucocorticoid therapy, response to","['GCTR', 'glucocorticoid therapy, response to']",,614400,,,"['-0.02997', '0.02324', '-0.01166', '0.00084', '0.006554', '-0.0435', '0.01863', '0.05368', '-0.0374', '-0.02715', '-0.01111', '0.01382', '0.01267', '0.01171', '-0.02281', '-0.0425', '-0.001761', '-0.02274', '-0.0226', '-0.09314', '-0.00432', '-0.03793', '0.03763', '-0.02864', '-0.001235', '-0.02254', '-0.00843', '-0.02309', '-0.006805', '-0.0421', '0.0505', '0.02263', '0.04724', '0.002407', '0.00916', '-0.01566', '-0.01462', '-0.0185', '-0.007267', '-0.0396', '0.0448', '-0.0497', '0.0237', '-0.011604', '0.006943', '-0.0375', '-0.000564', '0.00927', '0.01147', '0.04752', '-0.001025', '-0.02414', '0.00561', '0.01729', '-0.03513', '0.00547', '0.02759', '-0.03897', '-0.06647', '0.00881', '0.03174', '0.03038', '0.007694', '0.01438', '0.004818', '0.01617', '0.05884', '0.02438', '-0.03195', '0.0485', '-0.0283', '0.00433', '0.00699', '-0.02339', '0.02693', '0.03848', '0.01648', '-0.031', '-0.01539', '-0.02974', '0.007008', '0.001723', '-0.00896', '0.03897', '-0.003735', '-0.005016', '0.02217', '0.01794', '0.05066', '0.01678', '0.02614', '0.03262', '-0.02104', '-0.004333', '0.0867', '0.02939', '0.04468', '-0.04752', '-0.01318', '0.015526']",,,,,,,
mondo:0013734,"microphthalmia, syndromic 11","['microphthalmia, syndromic type 11', 'VAX1 syndromic microphthalmia', 'MCOPS11', 'microphthalmia, syndromic 11', 'syndromic microphthalmia caused by mutation in VAX1']",0111804,614402,,C3553077,,,,,,,,
mondo:0013735,microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome,"['microcephaly, cerebellar hypoplasia, and CARDIAC conduction defect syndrome', 'MCHCCD', 'Zaki-Gleeson syndrome', 'microcephaly-cerebellar hypoplasia-congenital heart conduction defect syndrome']",,614407,329332,C3280692,,,,,,,,
mondo:0013737,hereditary spastic paraplegia 46,"['autosomal recessive spastic paraplegia type 46', 'GBA2 autosomal recessive complex spastic paraplegia', 'autosomal recessive spastic paraplegia 46', 'hereditary spastic paraplegia type 46', 'spastic paraplegia 46, autosomal recessive', 'SPG46', 'autosomal recessive complex spastic paraplegia caused by mutation in GBA2']",0110798,614409,320391,C4510081,"['-0.2391', '-0.001393', '0.01474', '-0.7256', '-0.1581', '-0.4873', '-0.1249', '0.1506', '-1.082', '-0.2094', '-0.0854', '-0.446', '-0.3384', '-0.09644', '0.4468', '-0.266', '-0.1176', '-0.5054', '-0.3293', '-0.1895', '0.262', '-0.2815', '0.02214', '0.0784', '0.1881', '0.06354', '0.1786', '0.2522', '0.08234', '-0.2527', '0.2747', '0.2659', '0.2576', '-0.05743', '0.03928', '-0.3232', '-0.35', '0.1332', '-0.3088', '-0.268', '0.262', '-0.584', '0.1908', '0.5273', '-0.2041', '-0.52', '-0.04712', '0.0505', '0.3027', '0.1129', '0.209', '0.3833', '-0.2822', '-0.452', '-0.316', '-0.06223', '0.667', '-0.1175', '-0.2803', '0.2542', '-0.3303', '0.05444', '0.4985', '0.2742', '-0.3682', '0.3748', '0.3176', '0.768', '-0.2996', '0.311', '-0.3884', '0.744', '0.2092', '-0.0371', '0.2815', '0.1655', '-0.0863', '0.3757', '0.0701', '-0.1396', '-0.08795', '-0.1323', '0.3337', '0.3545', '-0.096', '0.2339', '0.10626', '0.0729', '0.4722', '-0.1256', '0.2651', '0.1501', '0.04462', '-0.06238', '0.4124', '0.3188', '0.702', '0.1727', '0.4211', '0.3774']",,,,,,,
mondo:0013738,autosomal recessive nonsyndromic hearing loss 96,"['autosomal recessive nonsyndromic deafness type 96', 'autosomal recessive nonsyndromic deafness 96', 'deafness, autosomal recessive 96', 'DFNB96', 'autosomal recessive deafness 96']",0110538,614414,,,,,,,,,,
mondo:0013739,chilblain lupus 2,"['SAMHD1 chilblain lupus', 'CHBL2', 'chilblain lupus caused by mutation in SAMHD1', 'Chilblain lupus type 2', 'chilblain lupus 2']",,614415,,C3280721,,,,,,,,
mondo:0013740,lethal occipital encephalocele-skeletal dysplasia syndrome,"['RHFCA', 'craniosynostosis with radiohumeral fusions and other skeletal and craniofacial anomalies', 'radiohumeral fusions with other skeletal and craniofacial anomalies']",,614416,293925,C3280729,"['-0.5244', '-0.1365', '0.3916', '-0.2122', '0.2454', '-0.2764', '0.0578', '0.6963', '-0.312', '-0.10614', '-0.4543', '-0.281', '-0.07635', '-0.1246', '-0.09216', '-0.171', '0.3313', '-0.04596', '-0.2688', '-0.628', '-0.0868', '0.0837', '0.6025', '-0.3389', '0.2296', '0.1499', '0.03098', '0.0712', '0.1273', '-0.1383', '0.1191', '-0.2817', '0.2087', '0.3372', '0.3743', '-0.06635', '0.1761', '-0.2996', '-0.11053', '-0.3118', '-0.09796', '-0.1445', '0.1091', '-0.1498', '0.000282', '-0.3804', '-0.1854', '0.497', '-0.1047', '0.07855', '0.1105', '-0.183', '0.1589', '0.0858', '-0.4084', '-0.5205', '-0.09424', '-0.1427', '-0.2524', '0.12445', '0.26', '-0.0864', '-0.2147', '-0.02592', '-0.2094', '-0.1368', '0.2869', '0.146', '-0.3535', '0.2644', '-0.2976', '0.1139', '0.1912', '-0.011024', '-0.27', '-0.1101', '-0.02805', '-0.1333', '-0.391', '-0.4517', '0.006638', '0.295', '0.1752', '0.3928', '-0.08417', '-0.2233', '-0.093', '0.168', '0.1621', '-0.338', '-0.1497', '0.1985', '0.07654', '0.09467', '0.354', '0.0183', '0.904', '-0.51', '0.51', '0.2471']",,,,,,,
mondo:0013741,familial temporal lobe epilepsy 5,"['epilepsy, familial temporal lobe, 5', 'ETL5', 'familial temporal lobe epilepsy type 5', 'epilepsy, familial temporal lobe, type 5']",0060752,614417,,C3280730,,,,,,,,
mondo:0013742,familial mesial temporal lobe epilepsy with febrile seizures,"['FEB11', 'febrile seizures, familial, type 11', 'febrile seizures, familial, 11']",,,165805,,"['0.3643', '0.2476', '-0.611', '0.05643', '-0.694', '-0.4417', '0.922', '0.4353', '-0.4304', '-0.433', '0.124', '0.8804', '-0.2827', '0.1637', '-0.3823', '-0.2642', '-0.3806', '-0.2776', '-0.2402', '-0.8447', '0.1209', '0.178', '-0.2399', '-0.1813', '-0.331', '0.09827', '-0.878', '0.0845', '-0.53', '-0.2092', '0.24', '-0.8003', '0.00948', '0.4111', '-0.805', '0.308', '-0.8774', '-0.267', '-0.2461', '-0.6724', '0.3088', '-0.301', '0.4668', '-0.468', '0.4316', '0.1442', '-0.668', '-0.1877', '-0.211', '0.5684', '-0.6343', '0.209', '0.0906', '0.08514', '0.0933', '0.2013', '-0.2163', '0.652', '-0.1826', '0.7686', '-0.273', '0.4006', '0.8877', '0.5225', '-0.2856', '0.08716', '0.7476', '-0.1075', '-0.7188', '0.757', '0.336', '0.596', '0.3992', '-0.584', '0.1603', '1.149', '0.1722', '0.1328', '0.5503', '0.287', '-0.158', '0.346', '-0.1353', '0.05234', '0.3423', '0.1504', '0.2451', '0.3704', '-0.2213', '0.729', '-0.2878', '0.87', '0.1296', '-0.03406', '0.4902', '0.3772', '0.729', '-0.519', '-0.07654', '-0.8105']",,,,,,,
mondo:0013743,autosomal systemic lupus erythematosus type 16,"['systemic lupus erythematosus type 16', 'familial systemic lupus erythematosus', 'familial SLE', 'autosomal SLE', 'systemic lupus erythematosus 16', 'SLEB16']",,614420,300345,C3280742,"['0.535', '-0.3557', '-0.302', '-0.0808', '-0.011375', '-0.3545', '-0.08746', '-0.1963', '-0.5923', '0.2524', '0.118', '-0.1859', '-0.0801', '0.07367', '-0.5923', '-0.3977', '-0.03824', '0.4045', '-0.382', '-0.6797', '-0.457', '-0.1483', '0.2084', '-1.018', '-0.0893', '-0.1951', '-0.1287', '0.07623', '-0.3533', '0.0671', '0.95', '-0.2922', '0.943', '-0.4414', '0.1305', '-0.10156', '-0.3962', '0.1039', '0.157', '-0.2318', '0.285', '-0.0769', '0.2979', '-0.4329', '-0.1885', '0.02715', '-0.02882', '-0.00988', '-0.001717', '0.1344', '-0.2537', '0.001115', '0.4624', '-0.122', '-0.0556', '0.4211', '-0.4373', '0.358', '-0.4048', '-0.575', '0.2063', '0.1936', '-0.13', '-0.1309', '-0.741', '0.1613', '0.408', '1.043', '-0.2974', '0.62', '0.03305', '0.09357', '-0.1835', '-0.05573', '0.2642', '0.4087', '0.4238', '0.7637', '0.6753', '-0.5215', '-0.1687', '-0.4607', '0.0638', '-0.366', '0.576', '-0.1992', '0.03111', '0.2917', '0.312', '0.284', '0.5376', '0.05145', '0.2834', '0.616', '0.469', '0.784', '-0.07385', '0.00287', '-0.0828', '-0.2908']",,,,,,,
mondo:0013744,cataract 37,"['cataract 37, autosomal dominant', 'CCA5', 'cataract 37', 'CTRCT37', 'cataract type 37', 'congenital cataract cerulean type 5', 'cataract, congenital, cerulean type, 5']",0110252,614422,,C3280758,,,,,,,,
mondo:0013745,Joubert syndrome 14,"['JBTS14', 'Joubert syndrome 14', 'Joubert syndrome caused by mutation in TMEM237', 'Joubert syndrome type 14', 'TMEM237 Joubert syndrome']",0110983,614424,220497,C3280766,"['-0.3706', '0.136', '-0.1827', '0.01828', '-0.3188', '-0.6934', '-0.2815', '0.4897', '-0.3477', '-0.4517', '-0.5244', '-0.6733', '-0.3926', '0.0906', '0.2477', '-0.5137', '0.1504', '-0.04532', '0.2937', '-1.083', '-0.1693', '-0.02684', '0.3167', '-0.2598', '0.351', '0.3425', '-0.3538', '0.2222', '0.219', '0.1133', '0.2402', '0.3486', '0.5645', '-0.03387', '0.1492', '-0.01254', '-0.2637', '0.05426', '-0.2098', '-0.00621', '0.07776', '0.07385', '0.4126', '0.07043', '0.2698', '-0.2676', '0.02834', '0.2264', '0.1152', '0.2471', '0.0805', '0.7446', '-0.3381', '-0.6133', '0.01921', '-0.6357', '0.1438', '0.1012', '-0.2235', '0.1515', '0.4685', '0.2896', '0.5894', '-0.2482', '0.11163', '-0.2211', '0.4092', '0.0726', '-0.512', '0.347', '-0.3372', '0.03128', '0.2164', '0.4973', '0.2866', '0.291', '0.7324', '0.1338', '-0.2612', '0.506', '0.1876', '-0.01477', '0.06665', '0.1403', '-0.00552', '-0.4941', '0.5303', '0.594', '0.3547', '0.1991', '-0.04556', '0.4395', '0.2686', '0.11426', '0.1296', '-0.0468', '0.552', '-0.1986', '0.01378', '0.4795']",,,,,,,
mondo:0013746,ventricular septal defect 1,"['VSD1', 'ventricular septal defect 1', 'ventricular septal defect type 1', 'GATA4 ventricular septal defect (disease)']",,614429,,C3280777,,,,,,,,
mondo:0013747,atrioventricular septal defect 4,"['atrioventricular septal defect caused by mutation in GATA4', 'GATA4 atrioventricular septal defect', 'atrioventricular septal defect type 4', 'atrioventricular septal defect 4', 'AVSD4']",,614430,,C3280781,,,,,,,,
mondo:0013748,ventricular septal defect 2,"['VSD2', 'ventricular septal defect type 2', 'ventricular septal defect 2', 'CITED2 ventricular septal defect (disease)']",,614431,,,,,,,,,,
mondo:0013749,ventricular septal defect 3,"['ventricular septal defect 3', 'ventricular septal defect type 3', 'VSD3', 'NKX2-5 ventricular septal defect (disease)']",,614432,,C3280785,,,,,,,,
mondo:0013750,atrial septal defect 8,"['ASD8', 'atrial septal defect type 8', 'atrial septal defect 8', 'atrial heart septal defect type 8', 'atrial heart septal defect caused by mutation in CITED2', 'CITED2 atrial heart septal defect']",0110113,614433,,,,,,,,,,
mondo:0013751,"cutis laxa, autosomal dominant 2","['cutis laxa, autosomal dominant type 2', 'autosomal dominant cutis laxa 2', 'FBLN5 autosomal dominant cutis laxa', 'ADCL2', 'cutis laxa, autosomal dominant 2', 'autosomal dominant cutis laxa caused by mutation in FBLN5']",0070136,614434,,C3280794,,,,,,,,
mondo:0013752,hypoplastic left heart syndrome 2,"['hypoplastic left heart syndrome type 2', 'HLHS2', 'NKX2-5 hypoplastic left heart syndrome', 'hypoplastic left heart syndrome caused by mutation in NKX2-5', 'hypoplastic left heart syndrome 2']",,614435,,C3280795,,,,,,,10021076,
mondo:0013753,Charcot-Marie-Tooth disease axonal type 2P,"['Charcot-Marie-Tooth disease caused by mutation in LRSAM1', 'Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive', 'Charcot-Marie-Toothe disease, axonal, type 2P', 'autosomal dominant Charcot-Marie-Tooth disease type 2G', 'CMT2P', 'Charcot-Marie-Tooth neuropathy type 2P', 'Charcot-Marie-Tooth neuropathy, type 2P', 'Charcot-Marie-Tooth disease type 2G', 'Charcot-Marie-Tooth disease, axonal, type 2G', 'Charcot-Marie-Tooth disease, axonal, type 2G, formerly', 'Charcot-Marie-Tooth disease type 2P', 'Charcot Marie Tooth disease type 2G', 'CMT2G', 'LRSAM1 Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth neuropathy, type 2G', 'CMT 2G', 'Charcot-Marie-Tooth disease, type 4A, axonal form', 'Charcot-Marie-Tooth disease, axonal, type 2P']",0110169,614436,99941,C4304674,"['0.04367', '0.03958', '0.06335', '-0.03394', '-0.02263', '-0.2654', '-0.07355', '0.4702', '-0.8613', '0.015564', '0.123', '0.2896', '-0.3276', '0.0447', '-0.2102', '-0.2578', '-0.2251', '-0.4316', '-0.552', '-0.73', '-0.03778', '0.315', '0.1809', '0.6045', '0.2334', '0.506', '-0.01089', '-0.06415', '-0.0622', '-0.1547', '0.006214', '-0.5967', '0.1399', '0.1953', '0.1857', '-0.732', '-0.5312', '-0.2112', '0.4075', '-0.2451', '-1.469', '-0.3425', '-0.3657', '0.633', '-0.1538', '-0.3235', '0.05518', '-0.10406', '-0.0826', '0.2249', '-0.0702', '0.336', '-0.2488', '-1.202', '0.003225', '-0.2856', '0.05545', '0.0931', '-0.7295', '0.0821', '-0.438', '0.3567', '0.8857', '0.739', '-0.9155', '0.9644', '-0.1093', '0.754', '-0.4197', '0.5024', '-1.087', '0.0744', '0.3198', '-0.2378', '0.9746', '0.4685', '-0.2551', '0.425', '0.3528', '-0.1848', '-0.1674', '0.0622', '1.102', '0.4297', '-0.05878', '-0.06042', '0.0399', '0.5186', '0.78', '0.1908', '0.2161', '-0.3', '-0.0002692', '0.4377', '0.6167', '0.3909', '0.769', '-0.4985', '-0.2196', '0.5566']",,,,,,,
mondo:0013754,"cutis laxa, autosomal recessive, type 1B","['cutis laxa, autosomal recessive, type IB', 'ARCL1B', 'autosomal recessive cutis laxa type IB']",0070133,614437,,C3280798,,,,,,,,
mondo:0013755,PYCR1-related de Barsy syndrome,"['ARCL3B', 'de Barsy syndrome caused by mutation in PYCR1', 'pyrroline-5-carboxylate reductase 1 deficiency', 'PYCR1 de Barsy syndrome', 'PYCR1 deficiency', 'autosomal recessive cutis laxa type IIIB', 'cutis laxa, autosomal recessive, type 3B', 'De Barsy syndrome B', 'cutis laxa, autosomal recessive, type IIIB']",0070138,614438,293633,C3280799,"['-0.1649', '0.1677', '-0.01605', '-0.02034', '0.001791', '-0.2866', '-0.001059', '0.1555', '-0.2144', '-0.1037', '-0.03616', '-0.06866', '-0.05777', '0.0399', '0.0861', '-0.1345', '-0.08234', '-0.1234', '-0.02917', '-0.281', '0.1094', '0.01732', '0.05206', '-0.09503', '0.1492', '0.07587', '-0.0938', '0.02348', '0.105', '-0.00805', '0.1214', '0.02716', '0.1907', '0.1216', '0.1256', '-0.1251', '0.1013', '-0.1088', '0.0415', '-0.1926', '0.139', '-0.2441', '0.0764', '-0.06323', '-0.002659', '-0.1947', '-0.001421', '0.0762', '0.1048', '-0.05823', '-0.00664', '-0.0903', '0.0005665', '0.0612', '-0.1412', '-0.1072', '0.3672', '0.04367', '-0.193', '0.10864', '0.05914', '0.05554', '0.03488', '-0.0003083', '0.08374', '0.1134', '0.1606', '0.0778', '-0.10077', '0.177', '-0.311', '0.0003119', '0.09125', '-0.11896', '0.04633', '0.0488', '0.00821', '-0.0499', '-0.1482', '0.03503', '0.07947', '0.05237', '-0.1323', '0.1117', '-0.0367', '-0.1467', '0.1715', '0.3525', '0.2034', '0.1986', '0.0918', '0.0538', '0.0712', '-0.08405', '0.4487', '0.0705', '0.2676', '-0.454', '0.02846', '0.02315']",,,,,,,
mondo:0013756,"hypertrophic osteoarthropathy, primary, autosomal recessive, 2","['PDP, autosomal recessive', 'SLCO2A1 primary hypertrophic osteoarthropathy', 'pachydermoperiostosis, autosomal recessive', 'hypertrophic osteoarthropathy, primary, autosomal recessive 2', 'hypertrophic osteoarthropathy, primary, autosomal recessive, 2', 'hypertrophic osteoarthropathy, primary, autosomal recessive, type 2', 'primary hypertrophic osteoarthropathy caused by mutation in SLCO2A1', 'PHOAR2']",,614441,,C3280800,,,,,,,,
mondo:0013757,congenital nongoitrous hypothryoidism 6,"['hypothyroidism, congenital, nongoitrous caused by mutation in THRA', 'CHNG6', 'hypothyroidism, congenital, nongoitrous, 6', 'THRA hypothyroidism, congenital, nongoitrous', 'congenital nongoitrous hypothyroidism 6', 'hypothyroidism, congenital, nongoitrous, type 6']",0070128,614450,,C3280817,,,,,,,,
mondo:0013758,Charcot-Marie-Tooth disease dominant intermediate E,"['Charcot-Marie-Tooth disease-nephropathy syndrome', 'Charcot-Marie-Tooth disease, dominant intermediate E', 'CMTDIE', 'autosomal dominant intermediate Charcot-Marie-Tooth disease type E', 'Charcot-Marie-Tooth disease, dominant Intermediate type E', 'Charcot-Marie-Tooth disease - nephropathy', 'Charcot-Marie-Tooth disease dominant intermediate type E', 'Charcot-Marie-Tooth neuropathy with focal segmental glomerulonephritis']",0110205,614455,93114,C4302667,"['0.4387', '0.01987', '-0.02814', '-0.3047', '-0.1798', '-0.4465', '-0.2076', '0.964', '-0.4321', '0.0366', '-0.1383', '0.11523', '-0.2788', '0.1818', '0.1914', '-0.0787', '0.1225', '-0.602', '-0.1338', '-0.1252', '0.2491', '0.3193', '0.279', '0.3438', '0.641', '0.237', '0.2018', '0.3015', '0.127', '0.02979', '0.3464', '-0.572', '0.1879', '-0.2922', '0.3367', '-1.024', '-0.3647', '-0.2585', '0.5596', '0.1098', '-1.392', '-0.6934', '-0.3953', '-0.00599', '-0.2715', '0.02078', '-0.1544', '-0.4575', '-0.4097', '-0.1854', '0.07074', '0.3547', '-0.1581', '-0.855', '-0.05383', '-0.1511', '0.3225', '-0.3977', '-0.8057', '-0.1256', '-0.1581', '-0.3848', '0.2313', '0.2837', '-0.539', '0.687', '-0.1725', '1.08', '-0.498', '0.348', '-0.878', '0.1442', '0.3293', '0.3738', '1.076', '0.8413', '-0.0744', '0.6997', '0.3381', '0.2069', '-0.1516', '0.07635', '1.227', '0.597', '-0.1467', '-0.4565', '0.2411', '0.8945', '0.345', '0.658', '0.4995', '-0.0783', '-0.2878', '0.3489', '0.4932', '0.52', '0.615', '-0.7095', '-0.05637', '0.5977']",,,,,,,
mondo:0013759,"melanoma, cutaneous malignant, susceptibility to, 8","['melanoma, cutaneous malignant, susceptibility to, type 8', 'CMM8', 'MITF-related melanoma and renal cell carcinoma predisposition syndrome', 'melanoma and renal cell carcinoma, susceptibility to', 'melanoma, cutaneous malignant, susceptibility to, 8', 'susceptibility to cutaneous malignant melanoma 8']",,614456,293822,,"['0.34', '-0.1186', '-0.7275', '0.235', '0.5884', '0.1581', '-0.3015', '0.4028', '-0.4626', '-0.2993', '1.186', '0.08044', '-0.6084', '0.3367', '-0.883', '-0.3687', '0.3518', '-0.4739', '-0.09204', '0.108', '-0.02368', '0.3108', '-0.3044', '-0.3074', '0.293', '-0.5527', '-0.785', '-0.102', '0.2866', '0.0255', '0.968', '-0.8433', '0.1774', '-0.2942', '0.2737', '0.6157', '-0.5557', '-0.276', '0.0926', '-0.4177', '0.4634', '-0.817', '0.06287', '-0.3643', '-0.1211', '-0.438', '-0.001698', '-0.393', '-0.03836', '-0.547', '0.2021', '-0.1917', '0.1769', '-0.592', '-1.065', '-0.3135', '-0.04123', '-0.02583', '-0.8364', '-0.5225', '-0.03534', '-0.1164', '-0.912', '0.4148', '3.98e-05', '1.3', '0.6514', '0.676', '0.2205', '1.057', '0.167', '0.641', '0.4663', '0.1785', '0.4998', '0.2229', '-0.9844', '0.6265', '0.01855', '-0.01181', '0.0907', '-0.0897', '0.2003', '-0.05847', '-0.1615', '-0.9077', '0.1091', '0.57', '1.141', '0.1184', '0.8926', '0.01733', '-0.4304', '0.4043', '0.635', '0.4678', '-0.2363', '-0.942', '-1.055', '0.594']",,,,,,,
mondo:0013760,congenital ichthyosis-intellectual disability-spastic quadriplegia syndrome,"['ichthyosis, spastic quadriplegia, and mental retardation', 'congenital ichthyosis-intellectual disability-spastic tetraplegia syndrome', 'ISQMR', 'ichthyosis, spastic quadriplegia, and intellectual disability']",,614457,352333,C3280856,"['-0.1054', '0.2034', '0.0556', '-0.1615', '0.001763', '-0.2761', '-0.007763', '0.165', '-0.1273', '-0.1514', '-0.08563', '-0.03918', '-0.007313', '-0.0925', '0.07605', '-0.0439', '0.0324', '-0.05817', '-0.0982', '-0.371', '-0.0493', '0.01683', '0.01545', '-0.0687', '0.09784', '0.02965', '-0.1381', '0.00727', '0.08826', '-0.157', '0.1078', '0.05804', '0.2922', '0.09924', '0.03415', '-0.1198', '-0.05292', '-0.287', '-0.02704', '-0.1831', '0.09503', '-0.2137', '-0.09326', '0.0247', '-0.0407', '-0.1628', '-0.1022', '0.1317', '-0.04977', '-0.0426', '-0.1192', '0.06082', '0.0041', '-0.12225', '-0.0755', '-0.02365', '0.1694', '-0.013885', '-0.151', '0.1356', '0.0699', '0.0691', '0.04834', '0.0763', '-0.1066', '0.02379', '0.219', '0.1912', '-0.2368', '0.1115', '-0.2241', '0.01409', '0.002337', '-0.1864', '0.08435', '-0.001194', '0.09344', '-0.0294', '-0.04425', '0.02019', '0.006123', '0.09576', '-0.1077', '0.2766', '0.02597', '0.07404', '-0.0173', '0.2332', '0.0662', '0.1129', '0.1956', '0.2177', '0.06824', '0.056', '0.3293', '0.03583', '0.2424', '-0.255', '0.1188', '0.0945']",,,,,,,
mondo:0013761,childhood encephalopathy due to thiamine pyrophosphokinase deficiency,"['THMD5', 'encephalopathy, episodic, due to thiamine pyrophosphokinase deficiency', 'thiamine metabolism dysfunction syndrome 5 (episodic encephalopathy type)']",,614458,293955,C3280866,"['-0.2197', '0.1356', '-0.002956', '-0.1547', '-0.3013', '-0.4375', '0.00682', '0.08435', '-0.2399', '0.2053', '-0.3716', '0.11487', '-0.1001', '-0.09344', '0.2166', '-0.0626', '0.06158', '-0.3032', '-0.2751', '-0.758', '0.03055', '0.04343', '0.2198', '-0.1024', '-0.0729', '-0.2239', '0.02351', '0.00963', '-0.1895', '-0.2026', '-0.1604', '0.4282', '0.312', '0.3628', '-0.1255', '-0.03775', '-0.1483', '-0.025', '-0.399', '0.1317', '0.2896', '-0.3489', '-0.1613', '0.1365', '-0.0971', '-0.1466', '-0.1562', '0.2194', '-0.2651', '0.3704', '-0.2869', '0.07806', '0.01956', '-0.1862', '0.10254', '-0.0513', '0.4146', '-0.1722', '-0.177', '0.274', '-0.01557', '0.2328', '0.45', '-0.2456', '-0.189', '-0.1096', '0.382', '0.4683', '-0.1863', '0.3765', '-0.077', '0.26', '-0.01672', '-0.3513', '0.0696', '-0.00451', '0.488', '-0.0881', '0.1418', '0.0318', '0.001704', '-0.0961', '0.10034', '0.2551', '0.597', '0.04904', '-0.1604', '-0.001638', '0.6196', '0.3', '0.4182', '0.3833', '-0.01469', '-0.126', '0.2703', '0.739', '0.483', '0.1065', '-0.0728', '0.3103']",,,,,,,
mondo:0013762,lipoic acid synthetase deficiency,"['HGCLAS', 'PDHLD', 'pyruvate dehydrogenase lipoic acid synthetase deficiency', 'hyperglycinemia, lactic acidosis, and seizures']",,614462,401859,C3280887,"['-0.2496', '0.6646', '0.1798', '-0.0941', '0.1821', '-0.5137', '-0.2068', '0.1807', '-0.633', '-0.1335', '-0.5186', '-0.5815', '0.189', '0.01758', '-0.0952', '0.12494', '-0.1324', '-0.2617', '-0.569', '-0.765', '-0.08014', '-0.3447', '0.2686', '0.08014', '-0.012314', '-0.1708', '-0.2563', '0.05853', '-0.03044', '0.1967', '0.3364', '0.3079', '0.1823', '0.0597', '-0.1542', '0.6216', '-0.0822', '0.2161', '0.2035', '0.2174', '0.3137', '-0.1527', '-0.07007', '0.352', '-0.6367', '-0.2074', '-0.3154', '-0.2489', '0.06396', '0.408', '-0.32', '0.1777', '0.0323', '-0.5674', '0.4084', '-0.2482', '0.1505', '0.367', '-0.1066', '0.4048', '0.01979', '0.3767', '0.5293', '0.07336', '-0.195', '0.1641', '0.11206', '0.1388', '-0.2937', '0.3801', '-0.11584', '-0.05695', '-0.296', '0.055', '0.02946', '0.06726', '0.2217', '-0.2139', '-0.05795', '0.00756', '0.1282', '-0.1567', '0.1392', '0.0035', '0.2308', '0.039', '0.06824', '0.3772', '0.585', '0.5913', '0.0857', '0.2448', '-0.1824', '0.00621', '0.281', '0.9375', '-0.1199', '-0.3484', '0.1838', '0.3118']",,,,,,,
mondo:0013763,Joubert syndrome 15,"['CEP41 Joubert syndrome', 'Joubert syndrome 15', 'JBTS15', 'Joubert syndrome 9/15, digenic', 'Joubert syndrome type 15', 'Joubert syndrome 12/15, digenic', 'Joubert syndrome caused by mutation in CEP41']",0110984,614464,,C3280897,,,,,,,,
mondo:0013764,Joubert syndrome 16,"['TMEM138 Joubert syndrome', 'Joubert syndrome 16', 'Joubert syndrome type 16', 'JBTS16', 'Joubert syndrome caused by mutation in TMEM138']",0110985,614465,,C3280906,,,,,,,,
mondo:0013765,"coronary heart disease, susceptibility to, 6","['susceptibility to coronary heart disease 6', 'MMP3 coronary artery disease', 'CHDS6', 'coronary artery disease caused by mutation in MMP3', 'coronary heart disease, susceptibility to, 6', 'coronary heart disease, susceptibility to, type 6']",,614466,,,,,,,,,,
mondo:0013766,familial cold autoinflammatory syndrome 3,"['PLCG2 familial cold autoinflammatory syndrome', 'familial cold autoinflammatory syndrome type 3', 'familial cold autoinflammatory syndrome caused by mutation in PLCG2', 'plaid', 'familial atypical cold urticaria', 'FACU', 'antibody deficiency and immune dysregulation, PLCG2-associated', 'PLCG2-associated antibody deficiency and immune dysregulation', 'FCAS3', 'familial cold urticaria with common variable immunodeficiency', 'familial cold autoinflammatory syndrome 3']",0090064,614468,300359,C3280914,"['-0.1069', '0.2406', '-0.1938', '-0.257', '-0.134', '-0.3977', '-0.03058', '-0.2449', '-0.1643', '0.2246', '0.10315', '0.6025', '0.04865', '-0.3442', '-0.1407', '0.624', '0.1826', '-0.1613', '-0.809', '-0.802', '-0.001', '-0.1556', '0.4097', '-0.04733', '-0.268', '-0.1298', '-0.4727', '0.3', '0.1096', '-0.2319', '0.1392', '0.3872', '0.314', '0.3948', '0.3484', '-0.1696', '-0.2644', '-0.3962', '0.0448', '0.05026', '0.1626', '-0.1841', '0.0925', '0.11334', '-0.0769', '-0.06238', '-0.1041', '-0.0645', '0.3772', '0.3953', '-0.644', '-0.1786', '0.317', '0.4219', '-0.2286', '0.4058', '0.0616', '-0.0996', '-0.282', '0.04175', '0.5347', '0.5493', '-0.0726', '0.3372', '0.112', '0.12024', '1.086', '0.3552', '-0.3052', '0.551', '-0.5435', '-0.361', '-0.0949', '-0.2273', '0.1024', '-0.03854', '0.5', '0.2927', '0.5024', '0.1151', '0.03998', '0.02013', '0.0981', '0.2351', '-0.08936', '-0.0881', '-0.004124', '0.548', '0.3518', '0.4883', '0.848', '0.4375', '0.3228', '0.011986', '0.3657', '0.624', '0.162', '-0.1377', '-0.3352', '0.1293']",,,,,,,
mondo:0013767,autoimmune lymphoproliferative syndrome type 4,"['ALPS type 4', 'RAS-associated autoimmune leukoproliferative disorder', 'autoimmune lymphoproliferative syndrome caused by mutation in NRAS', 'ALPS4', 'autoimmune lymphoproliferative syndrome type IV', 'NRAS autoimmune lymphoproliferative syndrome', 'ALPS type IV', 'RAS-associated autoimmune lymphoproliferative syndrome type IV, somatic', 'RAS-associated autoimmune leukoproliferative disease', 'RALD', 'autoimmune lymphoproliferative syndrome, type 4', 'autoimmune lymphoproliferative syndrome type 4']",0110117,614470,268114,C2674723,"['0.0286', '0.01962', '-0.07623', '0.2537', '0.1026', '-0.2954', '-0.1302', '0.4607', '0.1769', '-0.732', '0.011925', '-0.07355', '-0.1233', '-0.2542', '0.467', '0.3716', '-0.383', '-0.4062', '-0.08453', '-0.558', '0.4834', '-0.437', '0.448', '-0.823', '0.6025', '0.2976', '-0.107', '-0.3953', '-0.3367', '-0.4907', '0.369', '0.6504', '0.4875', '0.3367', '0.4202', '-0.3882', '-0.732', '-0.4255', '0.02742', '-0.6', '-0.2979', '0.2101', '-0.1337', '-0.782', '-0.2125', '-0.272', '-0.0936', '-0.3445', '0.269', '0.4006', '0.1196', '0.293', '-0.0741', '0.1091', '-0.05646', '-0.354', '0.1982', '-0.249', '-0.1151', '0.7534', '0.1758', '-0.0864', '0.2158', '-0.2413', '0.00267', '-0.2932', '0.5605', '0.8604', '-0.1833', '0.2284', '-0.1982', '0.08185', '-0.427', '0.7607', '0.5054', '-0.01912', '-0.0003426', '0.502', '0.1002', '-0.46', '0.08356', '-0.1249', '-0.1167', '-0.0664', '-0.7407', '-0.4263', '0.65', '-0.005077', '0.3914', '-0.392', '0.555', '0.612', '-0.614', '0.1654', '0.4707', '0.895', '0.0938', '-0.1249', '-0.04214', '-0.2578']",,,,,,,
mondo:0013768,"arterial calcification, generalized, of infancy, 2","['arterial calcification of infancy caused by mutation in ABCC6', 'ABCC6 arterial calcification of infancy', 'arterial calcification, generalized, of infancy, 2', 'arterial calcification, generalized, of infancy, type 2', 'GACI2']",,614473,,C3276161,,,,,,,,
mondo:0013769,atrioventricular septal defect 5,"['atrioventricular septal defect caused by mutation in GATA6', 'GATA6 atrioventricular septal defect', 'atrioventricular septal defect 5', 'atrioventricular septal defect type 5', 'AVSD5']",,614474,,C3280939,,,,,,,,
mondo:0013770,atrial septal defect 9,"['atrial septal defect 9', 'GATA6 atrial heart septal defect', 'atrial heart septal defect type 9', 'atrial heart septal defect caused by mutation in GATA6', 'atrial septal defect type 9', 'ASD9']",0110114,614475,,C3280943,,,,,,,,
mondo:0013771,transient infantile hypertriglyceridemia and hepatosteatosis,"['hypertriglyceridemia, transient infantile', 'HTGTI', 'transient infantile hypertriglyceridemia and fatty liver']",,614480,300293,C3280953,"['-0.2024', '0.1313', '0.0808', '-0.143', '-0.01368', '-0.2698', '-0.0508', '0.3494', '-0.2', '0.1396', '-0.3958', '-0.02975', '-0.0707', '-0.1195', '-0.4646', '-0.3757', '0.09393', '0.03683', '-0.0741', '-0.5264', '0.1526', '-0.2517', '0.3276', '-0.03787', '0.00886', '0.0564', '0.1807', '0.10236', '-0.2242', '-0.2385', '0.333', '0.1576', '0.4834', '0.1526', '-0.1522', '-0.0764', '-0.382', '0.03937', '-0.1769', '-0.2832', '-0.1891', '-0.1544', '0.3542', '0.1853', '-0.3533', '-0.00975', '-0.146', '0.0667', '-0.169', '0.3303', '-0.03305', '0.1604', '0.1316', '-0.1814', '-0.1534', '-0.1418', '0.188', '-0.2783', '-0.4404', '0.07166', '0.1991', '0.196', '0.0069', '-0.3208', '0.1259', '-0.2142', '0.316', '0.2488', '-0.3186', '-0.002752', '-0.1522', '0.0989', '0.28', '-0.0514', '0.01173', '-0.1086', '0.2142', '-0.03973', '-0.03702', '-0.01019', '-0.1064', '0.1633', '-0.1486', '-0.3157', '0.3188', '0.3428', '0.0995', '0.2031', '0.429', '-0.0873', '0.3318', '0.2812', '-0.268', '0.1421', '0.4094', '0.2817', '0.1962', '-0.4048', '0.04398', '0.02646']",,,,,,,
mondo:0013772,congenital cataract-hearing loss-severe developmental delay syndrome,"['congenital cataract-deafness-severe developmental delay syndrome', 'CCHLND', 'lethal neurodegenerative disorder due to copper transport defect', 'congenital cataracts, hearing loss, and neurodegeneration']",,614482,300313,C3280965,"['0.698', '-0.07684', '0.4006', '0.5376', '-0.646', '0.2637', '0.7324', '0.9346', '-0.3013', '-0.7124', '-0.01901', '-0.1522', '-0.7266', '0.2053', '-0.3667', '-0.5806', '-0.4963', '-0.01776', '-0.6187', '-0.2334', '0.2563', '0.08997', '-0.7686', '0.4155', '0.975', '0.09283', '-0.9917', '-0.001858', '-0.754', '-0.1506', '0.1208', '-0.1147', '0.1797', '-0.1744', '-0.2268', '-0.11694', '-0.551', '-0.5454', '-0.2141', '-0.599', '0.1979', '-0.1843', '-0.3018', '-0.3486', '0.05026', '-0.685', '0.2308', '0.3774', '0.02928', '-0.2139', '-0.0082', '-0.2216', '-0.3286', '-0.06085', '0.268', '0.7993', '0.1135', '0.3613', '-0.4348', '0.4773', '-0.06726', '1.036', '-0.4875', '0.2252', '-0.3376', '0.1617', '-0.5874', '1.174', '-0.4854', '-0.3613', '0.123', '0.833', '1.122', '-0.903', '0.4768', '-0.01147', '1.133', '0.3882', '0.11316', '-0.1622', '0.1218', '-0.573', '-0.462', '0.9766', '0.1733', '-0.2264', '-0.11115', '1.469', '0.291', '0.5884', '0.3877', '0.318', '-0.2113', '0.525', '0.421', '0.0457', '-0.1544', '-1.376', '-0.252', '-0.1436']",,,,,,,
mondo:0013773,porencephaly 2,"['porencephaly 2', 'porencephaly caused by mutation in COL4A2', 'porencephaly type 2', 'COL4A2 porencephaly', 'brain small vessel disease 2', 'POREN2']",0112314,614483,,C3280970,,,,,,,,
mondo:0013774,trigonocephaly 2,"['isolated trigonocephaly caused by mutation in FREM1', 'TRIGNO2', 'FREM1 isolated trigonocephaly', 'trigonocephaly type 2', 'trigonocephaly 2', 'craniosynostosis, metopic']",,614485,,,,,,,,,,
mondo:0013775,thrombomodulin-related bleeding disorder,"['thrombomodulin-related coagulopathy', 'THPH12', 'thrombophilia due to thrombomodulin defect', 'THBD-related bleeding disorder', 'THBD-related coagulopathy', 'thrombophilia 12 due to thrombomodulin defect']",0111908,614486,436169,C3280976,,,,C566057,,,,
mondo:0013776,spastic ataxia 5,"['AFG3L2 autosomal recessive spastic ataxia', 'autosomal recessive spastic ataxia type 5', 'AFG3L2-related spastic ataxia-myoclonic epilepsy-neuropathy syndrome', 'SPAX5', 'autosomal recessive spastic ataxia caused by mutation in AFG3L2', 'AFG3L2-related spastic ataxia-neuropathy syndrome', 'spastic ataxia 5, autosomal recessive', 'spastic ataxia type 5', 'early-onset spastic ataxia-myoclonic epilepsy-neuropathy syndrome']",0050944,614487,313772,C3280977,"['-0.14', '-0.2957', '0.045', '0.04083', '-0.2338', '-0.9766', '0.2495', '-0.065', '-0.7676', '-0.8843', '-0.07324', '0.1213', '-0.0964', '0.3606', '0.4678', '-0.3557', '-0.174', '-0.2477', '0.1971', '-0.7656', '-0.0392', '-0.2734', '0.1688', '-0.527', '0.5156', '-0.5728', '-0.3162', '0.3096', '-0.03204', '-0.9243', '0.1666', '0.417', '-0.5923', '-0.1823', '0.3164', '0.1544', '-0.1896', '0.0782', '0.648', '0.4014', '0.3357', '0.1367', '-0.5303', '0.5015', '0.4265', '-0.5024', '0.0808', '0.4434', '0.4812', '-0.01907', '-0.2018', '0.272', '-0.1364', '-0.208', '0.02078', '-0.9155', '0.4077', '0.519', '-0.00778', '0.5444', '-0.3743', '0.2888', '0.4165', '-0.0574', '-0.5454', '0.5283', '0.1926', '0.6294', '-0.4495', '0.7', '0.812', '0.5825', '-0.1005', '-0.6978', '0.918', '0.357', '0.03226', '0.4329', '0.09814', '0.5576', '-0.4229', '-0.77', '0.4915', '0.9194', '-0.2844', '-0.8916', '0.2913', '-0.073', '0.5225', '0.4155', '0.5386', '0.424', '0.2954', '0.04453', '1.055', '1.013', '0.3164', '0.5156', '-0.629', '-0.05637']",,,,,G11.4,,
mondo:0013777,pseudohypoaldosteronism type 2B,"['WNK4 pseudohypoaldosteronism type 2', 'pseudohypoaldosteronism, type IIB', 'pseudohypoaldosteronism, type 2B', 'PHA2B', 'pseudohypoaldosteronism type 2 caused by mutation in WNK4']",,614491,88939,C1840390,"['-0.0951', '0.196', '-0.04715', '0.08203', '0.03503', '-0.3215', '-0.05258', '0.0688', '-0.3035', '-0.07196', '-0.1003', '0.01807', '-0.021', '0.03023', '0.06683', '-0.1506', '-0.05472', '-0.02576', '0.05057', '-0.2842', '0.093', '-0.0951', '0.2089', '0.00393', '0.1092', '0.05118', '-0.01779', '-0.05576', '0.04398', '-0.0925', '0.1652', '0.09436', '0.2307', '0.0904', '0.12445', '-0.2354', '0.0051', '-0.0796', '0.04047', '-0.1432', '0.07135', '-0.233', '0.1322', '0.07043', '-0.1588', '-0.2593', '0.03604', '0.08453', '0.0653', '-0.0369', '0.08575', '-0.1395', '0.07007', '-0.0932', '-0.1545', '-0.1453', '0.3074', '0.01409', '-0.2477', '0.1', '0.0455', '0.1255', '0.206', '-0.0883', '0.0946', '0.1069', '0.1338', '-0.10657', '-0.2214', '0.10944', '-0.2114', '-0.11096', '0.0689', '-0.1764', '0.2563', '0.007786', '-0.0944', '0.06256', '-0.1982', '0.02205', '-0.004192', '0.0318', '-0.0793', '0.0298', '-0.07074', '-0.078', '0.1921', '0.339', '0.2266', '0.1284', '0.02872', '0.00701', '0.10223', '-0.1998', '0.4243', '0.1959', '0.2085', '-0.371', '-0.0808', '0.0381']",,,C564161,,,,
mondo:0013778,pseudohypoaldosteronism type 2C,"['WNK1 pseudohypoaldosteronism type 2', 'pseudohypoaldosteronism, type IIC', 'pseudohypoaldosteronism, type 2C', 'PHA2C', 'pseudohypoaldosteronism type 2 caused by mutation in WNK1']",,614492,88940,C1840391,"['-0.10834', '0.1836', '-0.01591', '0.0784', '0.07806', '-0.328', '-0.0691', '0.11224', '-0.291', '-0.03937', '-0.1267', '-0.01278', '-0.05692', '0.05457', '0.08356', '-0.1378', '-0.05728', '-0.02843', '0.01572', '-0.2725', '0.07715', '-0.06824', '0.168', '0.0262', '0.09467', '0.05606', '-0.01591', '-0.01151', '0.04022', '-0.08624', '0.1774', '0.09546', '0.1953', '0.10376', '0.1354', '-0.2235', '0.01901', '-0.10846', '0.00883', '-0.1488', '0.04175', '-0.2369', '0.10486', '0.08594', '-0.1897', '-0.2344', '0.04727', '0.0985', '0.05087', '-0.00963', '0.076', '-0.1482', '0.07465', '-0.10944', '-0.1455', '-0.1382', '0.296', '-0.03696', '-0.2115', '0.0985', '0.06824', '0.09625', '0.1979', '-0.0821', '0.1063', '0.08826', '0.1611', '-0.05075', '-0.2037', '0.0915', '-0.2076', '-0.0687', '0.04208', '-0.1912', '0.2343', '0.03708', '-0.07764', '0.08386', '-0.1887', '0.05188', '0.01718', '0.00949', '-0.08026', '0.01575', '-0.0788', '-0.078', '0.2114', '0.3264', '0.208', '0.11224', '0.02312', '-0.00922', '0.05844', '-0.1782', '0.4146', '0.197', '0.2164', '-0.3748', '-0.0263', '0.04105']",,,C564162,,,,
mondo:0013779,Wiskott-Aldrich syndrome 2,"['Wiskott-Aldrich syndrome 2', 'WAS2', 'Wipf1 deficiency', 'WIPF1 Wiskott-Aldrich syndrome', 'Wiskott-Aldrich syndrome type 2', 'Wiskott-Aldrich syndrome caused by mutation in WIPF1']",,614493,,C3281001,,C176820,,,,,,
mondo:0013780,retinitis pigmentosa 63,"['retinitis pigmentosa type 63', 'retinitis pigmentosa 63', 'RP63']",0110385,614494,,C3281002,,,,,,H35.5,,
mondo:0013781,pseudohypoaldosteronism type 2D,"['familial hyperkalemic hypertension', 'pseudohypoaldosteronism, type 2D', 'pseudohypoaldosteronism, type IID', 'PHA2D', 'pseudohypoaldosteronism type 2 caused by mutation in KLHL3', 'KLHL3 pseudohypoaldosteronism type 2']",,614495,300525,C3469605,"['-0.0729', '0.2065', '-0.03497', '0.09827', '0.0598', '-0.3774', '-0.08795', '0.10065', '-0.3323', '-0.0833', '-0.124', '-0.00448', '-0.06015', '0.07904', '0.0985', '-0.1256', '-0.00976', '-0.01932', '0.007545', '-0.313', '0.053', '-0.06036', '0.1094', '0.05133', '0.07776', '0.04398', '-0.05017', '-0.03592', '0.04166', '-0.05756', '0.2179', '0.1426', '0.2322', '0.06305', '0.1223', '-0.2399', '0.003057', '-0.1531', '0.0496', '-0.1898', '0.07574', '-0.2416', '0.0783', '0.0618', '-0.2001', '-0.2223', '0.02461', '0.1348', '0.0964', '-0.07404', '0.0811', '-0.1455', '0.10864', '-0.0959', '-0.1752', '-0.1654', '0.2805', '0.01698', '-0.2379', '0.11053', '0.0703', '0.08936', '0.1703', '-0.0888', '0.05676', '0.1202', '0.1602', '-0.04562', '-0.2444', '0.066', '-0.2361', '-0.1133', '0.03217', '-0.2068', '0.2294', '0.007248', '-0.08923', '0.1271', '-0.1647', '0.02948', '0.02739', '0.00824', '-0.0677', '0.03693', '-0.06525', '-0.0973', '0.1896', '0.3804', '0.2291', '0.1608', '0.0592', '0.003963', '0.0803', '-0.1748', '0.4612', '0.2112', '0.2089', '-0.372', '-0.03174', '0.0579']",,,,,,,
mondo:0013782,pseudohypoaldosteronism type 2E,"['pseudohypoaldosteronism, type IIE', 'Cul3 pseudohypoaldosteronism type 2', 'pseudohypoaldosteronism type 2 caused by mutation in Cul3', 'CUL3 pseudohypoaldosteronism type 2', 'pseudohypoaldosteronism, type 2E', 'PHA2E']",,614496,300530,C3469606,"['-0.09827', '0.2161', '-0.04248', '0.1306', '0.0773', '-0.3916', '-0.0972', '0.1139', '-0.35', '-0.0473', '-0.1458', '0.03094', '-0.0434', '0.0638', '0.1196', '-0.1179', '-0.01172', '-0.02109', '0.0353', '-0.3325', '0.0696', '-0.06445', '0.1486', '0.0329', '0.08075', '0.0593', '-0.05243', '-0.03577', '0.0553', '-0.0605', '0.1865', '0.127', '0.2278', '0.07886', '0.1412', '-0.2455', '0.0422', '-0.1346', '0.07794', '-0.1758', '0.04507', '-0.2253', '0.0887', '0.05615', '-0.2269', '-0.2109', '0.0521', '0.1777', '0.07324', '-0.0872', '0.06445', '-0.1637', '0.0774', '-0.1099', '-0.203', '-0.177', '0.2788', '0.02554', '-0.254', '0.0937', '0.0589', '0.10925', '0.1758', '-0.0903', '0.0497', '0.12256', '0.1647', '-0.06506', '-0.276', '0.06757', '-0.2505', '-0.0955', '0.0667', '-0.2612', '0.2413', '0.02103', '-0.1214', '0.1399', '-0.1655', '0.004494', '0.0126', '0.01935', '-0.06696', '0.0704', '-0.0697', '-0.10895', '0.206', '0.402', '0.2522', '0.1483', '0.0831', '-0.004642', '0.08093', '-0.1503', '0.4624', '0.2267', '0.2299', '-0.4036', '-0.03998', '0.05927']",,,,,,,
mondo:0013783,"microphthalmia, isolated, with coloboma 7","['ABCB6 microphthalmia, isolated, with coloboma', 'MCOPCB7', 'microphthalmia, isolated, with coloboma type 7', 'microphthalmia, isolated, with coloboma 7', 'microphthalmia, isolated, with coloboma caused by mutation in ABCB6']",,614497,,C3281027,,,,,,,,
mondo:0013784,neonatal-onset encephalopathy with rigidity and seizures,"['rigidity and multifocal seizure syndrome, lethal neonatal', 'lethal neonatal spasticity-epileptic encephalopathy syndrome', 'lethal neonatal rigidity-multifocal seizure syndrome', 'RMFSL']",,614498,435845,C3281029,"['0.02173', '0.08716', '-0.3274', '0.0951', '-0.4429', '-0.3774', '0.1113', '0.5957', '-0.327', '-0.1019', '-0.1943', '-0.1617', '0.1033', '0.192', '0.2249', '-0.007328', '-0.1075', '-0.068', '-0.1637', '-0.511', '-0.02313', '-0.1011', '0.2761', '-0.04486', '0.3293', '-0.2028', '-0.06934', '0.1183', '-0.2216', '0.01182', '0.3723', '-0.1124', '0.423', '0.4253', '0.02388', '0.174', '-0.129', '-0.4307', '0.06464', '0.0779', '0.1411', '-0.2686', '-0.2213', '-0.0537', '-0.2747', '0.03183', '-0.4658', '0.10474', '-0.3977', '0.404', '-0.1719', '-0.1092', '-0.2283', '0.1284', '0.1018', '-0.11163', '-0.08484', '-0.275', '0.06055', '0.2439', '0.1813', '0.007225', '0.2366', '-0.1558', '-0.1549', '-0.0814', '0.4915', '0.2922', '-0.3406', '0.3713', '-0.1583', '0.10297', '-0.0125', '-0.03296', '0.05457', '-0.03372', '0.08997', '-0.1327', '-0.2428', '0.1344', '0.004944', '0.485', '-0.1167', '-0.0986', '0.2708', '0.212', '0.1575', '-0.05255', '0.485', '0.1586', '0.2568', '0.3123', '0.0787', '0.3208', '0.0998', '0.3657', '0.1938', '-0.2727', '0.309', '0.2627']",,0009144,,,,,
mondo:0013785,"intellectual disability, autosomal recessive 34","['intellectual disability, autosomal recessive 34', 'CRADD autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive type 34', 'MRT34', 'mental retardation, autosomal recessive 34', 'mental retardation, autosomal recessive 34, with variant lissencephaly', 'autosomal recessive non-syndromic intellectual disability caused by mutation in CRADD', 'intellectual disability, autosomal recessive 34, with variant lissencephaly', 'intellectual developmental disorder, autosomal recessive 34, with variant lissencephaly', 'intellectual disability, autosomal recessive type 34']",0081200,614499,,C3281044,,C153179,,,,,,
mondo:0013786,cone-rod dystrophy 16,"['cone-rod dystrophy type 16', 'CORD16', 'cone-rod dystrophy caused by mutation in C8orf37', 'retinal dystrophy with early macular involvement', 'C8orf37 cone-rod dystrophy', 'cone-rod dystrophy 16', 'retinitis pigmentosa 64']",0111022,614500,,C3281045,,,,,,,,
mondo:0013787,"psychomotor retardation, epilepsy, and craniofacial dysmorphism","['neurodevelopmental disorder with hypotonia, craniofacial abnormalities, and seizures', 'psychomotor retardation, epilepsy, and craniofacial dysmorphism', 'PMRED']",,614501,,C3281055,,,,,,,,
mondo:0013788,Usher syndrome type 3B,"['USH3B', 'Usher syndrome type IIIB', 'Usher syndrome caused by mutation in HARS', 'Usher syndrome, type 3B', 'USHER syndrome, type IIIB', 'HARS Usher syndrome']",0110842,614504,,C3281066,,,,,,H35.5,,
mondo:0013789,DDOST-congenital disorder of glycosylation,"['carbohydrate deficient glycoprotein syndrome type', 'CDG1R', 'congenital disorder of glycosylation type 1r', 'congenital disorder of glycosylation type Ir', 'CDG syndrome type Ir', 'congenital disorder of glycosylation, type Ir', 'carbohydrate deficient glycoprotein syndrome type Ir', 'CDG-Ir', 'DDOST-CDG (CDG-Ir)', 'DDOST-CDG']",0080569,614507,300536,C3281084,"['-0.3862', '0.1021', '0.2397', '-0.1226', '0.1532', '-0.507', '-0.1791', '0.2822', '-0.4175', '-0.1952', '-0.12', '-0.2157', '-0.02165', '-0.2064', '-0.313', '-0.10834', '0.1109', '-0.104', '-0.2825', '-0.7563', '0.1586', '-0.0893', '0.1829', '-0.1635', '0.194', '-0.01209', '-0.1731', '0.03032', '0.1785', '-0.1702', '0.3032', '0.3918', '0.582', '0.11066', '-0.07117', '-0.2198', '-0.2112', '-0.1129', '-0.392', '-0.1788', '-0.03766', '-0.2896', '0.1702', '0.1665', '-0.3118', '-0.06866', '0.02357', '0.0744', '0.401', '0.2803', '-0.2289', '0.2086', '-0.01059', '-0.0953', '-0.1385', '-0.2957', '0.1678', '0.1299', '-0.477', '0.3853', '0.294', '0.1414', '0.3914', '0.02666', '0.1293', '-0.157', '0.0631', '0.3157', '-0.5186', '0.03195', '-0.367', '0.2047', '0.2996', '0.0566', '0.0721', '-0.0017395', '0.533', '-0.1399', '-0.327', '0.3394', '0.2158', '-0.2058', '-0.11053', '0.1783', '0.0865', '-0.0478', '0.2925', '0.4556', '0.465', '0.2693', '0.1593', '0.4841', '-0.1096', '0.02771', '0.2932', '0.52', '0.5596', '-0.2979', '0.246', '0.3716']",,,,,,,
mondo:0013790,mirror movements 2,"['RAD51 familial congenital mirror movements', 'mirror movements type 2', 'MRMV2', 'familial congenital mirror movements caused by mutation in RAD51', 'mirror movements 2']",,614508,,C3281089,,,,,,,,
mondo:0013791,"thrombophilia due to protein S deficiency, autosomal recessive","['thrombophilia 5 due to protein S deficiency, autosomal recessive', 'thrombophilia due to PROTEIN S deficiency, autosomal recessive', 'THPH6', 'thrombophilia due to protein S deficiency, autosomal recessive']",,614514,,C3281092,,,,,,,,
mondo:0013792,intracerebral hemorrhage,"['ich', 'stroke, hemorrhagic, susceptibility to', 'hemorrhage, intracerebral, susceptibility to', 'stroke, hemorrhagic']",,614519,,,"['-0.11993', '0.0991', '-0.07104', '-0.09393', '-0.03708', '0.04214', '0.04834', '0.004658', '-0.1987', '0.1217', '-0.352', '-0.2817', '-0.03775', '-0.0744', '-0.1497', '-0.3154', '-0.03732', '-0.2812', '0.0654', '-0.4421', '-0.0991', '-0.06464', '0.2155', '-0.2063', '0.0994', '0.0197', '0.01251', '0.2302', '-0.0677', '0.05356', '0.03375', '-0.2407', '0.3552', '-0.01775', '0.11066', '0.1349', '-0.1293', '0.01685', '-0.004375', '-0.264', '0.2191', '-0.179', '0.04422', '-0.12384', '0.2593', '-0.1305', '-0.04974', '0.0609', '0.0664', '-0.006405', '0.2269', '0.02689', '0.001274', '0.154', '-0.1576', '-0.0001671', '0.2966', '0.00791', '-0.3435', '0.1881', '-0.1064', '0.01797', '0.1808', '-0.0691', '-0.2325', '-0.02167', '0.2583', '0.2793', '-0.1956', '0.3535', '-0.10065', '0.1827', '-0.07874', '-0.1858', '-0.007507', '0.1802', '0.2717', '0.2025', '-0.03433', '-0.313', '-0.4128', '-0.00861', '0.00222', '0.08936', '-0.00752', '-0.0907', '0.1525', '0.2583', '0.2698', '-0.2103', '0.0853', '0.3008', '0.04092', '-0.00177', '0.2366', '0.1442', '0.1908', '-0.2441', '-0.000719', '0.1898']",,0005669,D002543,431,,,
mondo:0013793,"encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency","['encephalomyopathy, mitochondrial, due to voltage-dependent anion channel deficiency']",,614520,,C3281106,,,,,,,,
mondo:0013794,thrombocythemia 3,"['thrombocythemia 3, autosomal dominant, somatic mutation', 'familial thrombocytosis caused by mutation in JAK2', 'thrombocytosis 3', 'thrombocythemia 3', 'THCYT3', 'JAK2 familial thrombocytosis', 'thrombocythemia type 3']",,614521,71493,C3281125,,,,,,,,
mondo:0013795,fibrochondrogenesis 2,"['FBCG2', 'fibrochondrogenesis 2', 'fibrochondrogenesis type 2', 'fibrochondrogenesis caused by mutation in COL11A2', 'COL11A2 fibrochondrogenesis']",0080673,614524,,C3281128,,,,,,,,
mondo:0013796,chromosome 17q12 duplication syndrome,"['17q12 microduplication syndrome', 'trisomy 17q12', '17q12 duplication', '17q12 microduplication', 'recurrent duplication of 17q12', 'dup(17)(q12)', 'chromosome 17q12 duplication syndrome']",0060433,614526,261272,C3281137,,,,,,,,
mondo:0013797,chromosome 17q12 deletion syndrome,"['17q12 deletion syndrome', 'monosomy 17q12', 'Del(17)(q12)', '17q12 recurrent deletion syndrome', 'chromosome 17q12 deletion syndrome', '17q12 microdeletion syndrome']",0060404,614527,261265,C4518822,,,,,,,,
mondo:0013798,chromosome 16q22 deletion syndrome,"['chromosome 16q22 deletion syndrome, isolated cases', 'chromosome 16q22 deletion syndrome']",0060401,614541,,C3281152,,,,,,,,
mondo:0013800,"Ehlers-Danlos syndrome, kyphoscoliotic and deafness type","['Ehlers-Danlos syndrome, kyphoscoliotic and hearing loss type', 'EDSKSCL2', 'EDS, kyphoscoliotic and hearing loss type', 'Ehlers-Danlos syndrome, kyphoscoliotic type, 2', 'Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and deafness', 'EDS with progressive kyphoscoliosis, myopathy, and deafness', 'EDS with progressive kyphoscoliosis, myopathy, and hearing loss', 'EDSKMH', 'Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss']",,614557,300179,C3281160,"['0.2498', '-0.01198', '-0.3845', '0.0535', '0.556', '-0.978', '0.1953', '0.4016', '-0.861', '0.602', '0.0617', '-0.4634', '-0.2175', '0.7627', '-0.545', '0.1886', '-0.6475', '0.2822', '0.04517', '-0.3708', '0.01805', '0.931', '0.3694', '0.03378', '-0.2732', '0.4084', '0.3245', '0.1642', '1.344', '0.5356', '1.127', '-0.2783', '0.0674', '0.2423', '0.0158', '-0.2979', '-0.559', '0.0623', '0.2915', '-0.901', '0.7563', '-0.3887', '-0.77', '0.3623', '0.0646', '-0.3381', '-0.2947', '0.706', '0.582', '-0.2502', '-0.1421', '-0.45', '0.6484', '-0.5234', '0.1365', '-0.614', '-0.514', '0.5625', '0.1925', '-0.1384', '-0.1307', '0.434', '-0.022', '-0.0476', '0.02974', '0.1731', '-0.472', '1.01', '-0.12244', '0.945', '-0.561', '0.1718', '-0.4075', '-0.3787', '-0.1186', '-0.5903', '-0.3792', '-0.1189', '0.0393', '-0.1641', '0.0616', '-0.4568', '0.1814', '0.571', '-0.743', '0.03223', '0.02034', '1.098', '-0.0845', '0.02367', '0.8706', '0.669', '-0.364', '0.5215', '0.6504', '-0.2598', '0.6343', '-0.0612', '0.528', '0.1367']",,,,,,,
mondo:0013801,"developmental and epileptic encephalopathy, 13","['epileptic encephalopathy, early infantile, 13', 'EIEE13', 'epileptic encephalopathy, early infantile, type 13', 'early infantile epileptic encephalopathy-13', 'early infantile epileptic encephalopathy caused by mutation in SCN8A', 'developmental and epileptic encephalopathy 13', 'SCN8A early infantile epileptic encephalopathy', 'SCN8A encephalopathy', 'SCN8A epilepsy', 'DEE13']",0080445,614558,,C3281191,,,,,,,,
mondo:0013802,infantile cerebellar-retinal degeneration,"['ICRD', 'infantile cerebellar retinal degeneration', 'infantile cerebellar-retinal degeneration']",0050883,614559,313850,C3281192,"['-0.05872', '0.3145', '-0.01599', '0.149', '0.221', '-0.6064', '0.04755', '-0.0812', '-0.769', '0.02051', '-0.2617', '-0.2227', '-0.02692', '-0.2896', '0.1382', '0.0847', '0.02986', '-0.4736', '-0.1779', '-0.885', '-0.2708', '-0.2437', '-0.1305', '-0.09576', '0.4854', '-0.2367', '-0.145', '0.3718', '-0.05502', '0.5337', '0.2094', '0.3718', '0.2083', '-0.1259', '0.422', '0.4458', '0.006943', '0.2678', '-0.05603', '-0.2274', '0.3865', '-0.3052', '-0.3706', '0.0798', '0.3928', '-0.3774', '0.2737', '0.2698', '0.298', '-0.1385', '0.02396', '-0.0578', '-0.233', '-0.6123', '0.3691', '-0.3025', '0.2122', '0.3137', '-0.0337', '0.11304', '-0.2654', '-0.3093', '0.3086', '-0.1067', '-0.5405', '0.1488', '0.4587', '0.581', '-0.3276', '-0.155', '-0.2722', '0.3213', '-0.1863', '-0.02702', '0.03366', '-0.0968', '0.545', '0.00665', '-0.379', '0.03177', '0.657', '-0.4595', '-0.3694', '0.5215', '-0.08044', '-0.3245', '0.1318', '0.616', '0.451', '0.654', '-0.002373', '0.4497', '-0.354', '0.099', '0.6816', '0.5786', '0.3667', '0.0831', '0.03943', '0.175']",,,,,,,
mondo:0013803,leukoencephalopathy with calcifications and cysts,"['Labrune syndrome', 'LCC', 'leukoencephalopathy, brain calcifications, and cysts']",,614561,542310,C3281200,,,,C000598644,,,,
mondo:0013805,"intellectual disability, autosomal dominant 13","['intellectual disability, autosomal dominant type 13', 'mental retardation, autosomal dominant 13, with neuronal migration defects', 'intellectual disability, autosomal dominant, 13, with neuronal migration defects', 'autosomal dominant mental retardation 13', 'mental retardation, autosomal dominant type 13', 'intellectual disability, autosomal dominant 13', 'MRD13', 'mental retardation, autosomal dominant 13', 'DYNC1H1 autosomal dominant non-syndromic intellectual disability', 'autosomal dominant non-syndromic intellectual disability 13', 'mental retardation, autosomal dominant, 13, with neuronal migration defects', 'intellectual disability, autosomal dominant 13, with neuronal migration defects', 'autosomal dominant non-syndromic intellectual disability caused by mutation in DYNC1H1', 'autosomal dominant intellectual disability 13']",0070043,614563,,C3281202,,,,,,,,
mondo:0013806,familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome,"['familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome', 'telangiectasia, cutaneous, and cancer syndrome, familial', 'FCTCS', 'cutaneous telangiectasia and cancer syndrome, familial']",,614564,313846,C3281203,"['0.2688', '-0.1197', '0.0782', '0.2517', '0.659', '-0.7583', '0.4275', '0.4722', '0.006798', '0.01689', '0.662', '0.1692', '-0.2856', '0.3752', '-0.2913', '-0.247', '-0.0513', '-0.496', '-0.8604', '-0.3179', '-0.0351', '-0.4587', '-0.559', '0.06744', '0.2532', '-0.531', '0.10455', '0.1417', '0.425', '-0.1301', '0.546', '-0.3867', '0.1438', '-0.92', '0.878', '-0.1141', '-0.841', '0.0227', '-0.4192', '-0.1273', '0.3962', '-0.1853', '0.0414', '-0.06256', '0.0873', '-0.1442', '-0.0911', '-0.9253', '1.295', '-0.562', '-0.2524', '-0.2903', '0.1638', '-0.05313', '-0.4255', '0.01721', '-0.2842', '0.06726', '-1.097', '-0.9136', '0.591', '-0.05695', '-0.2448', '-0.5', '-0.3027', '0.4382', '0.4253', '0.3423', '0.1149', '1.014', '-0.0424', '0.7363', '0.05124', '0.0754', '1.259', '0.2219', '-0.03854', '0.01619', '0.10583', '0.4224', '-0.0457', '0.2632', '-0.011055', '0.0636', '0.131', '-0.0671', '0.776', '0.3115', '0.611', '-0.46', '0.1669', '0.1484', '-0.1821', '0.3853', '0.05276', '0.3335', '-0.2168', '-0.8135', '-0.2732', '-0.1489']",,,,,,,
mondo:0013807,congenital stationary night blindness 1E,"['Csnb, complete, autosomal recessive', 'CSNB1E', 'GPR179 congenital stationary night blindness', 'congenital stationary night blindness caused by mutation in GPR179', 'night blindness, congenital stationary (complete), 1E, autosomal recessive', 'night blindness, congenital stationary, type 1E', 'congenital stationary night blindness type 1E', 'congenital stationary night blindness 1E autosomal recessive']",0110869,614565,,C3281215,,,,,,,,
mondo:0013808,Maffucci syndrome,"['multiple Angiomas and Endochondromas', 'chondrodysplasia with hemangioma', 'hemangiomata with Dyschondroplasia', 'Dyschondrodysplasia with hemangiomas', 'Maffucci type enchondromatosis', 'Dyschondroplasia and cavernous hemangioma', 'Maffucci^s anomalad', 'multiple enchondromatosis, Maffucci type', 'enchondromatosis with multiple cavernous hemangiomas', 'Maffucci syndrome', 'Kast syndrome', 'enchondromatosis with hemangiomata', 'Chondroplasia angiomatosis', 'hemangiomatosis Chondrodystrophica']",0060221,614569,163634,C0024454,,C3213,,,,,,
mondo:0013810,COG6-ongenital disorder of glycosylation,"['CDG IIL', 'CDG syndrome type IIL', 'CDGIIl', 'congenital disorder of glycosylation type IIL', 'CDG2L', 'COG6-CDG', 'congenital disorder of glycosylation type 2l', 'COG6-CDG (CDG-IIL)', 'congenital disorder of glycosylation, type IIL', 'CDG-IIL']",0070264,614576,464443,C3553230,,,,,,,,
mondo:0013811,combined oxidative phosphorylation defect type 9,"['COXPD9', 'MRPL3 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 9', 'combined oxidative phosphorylation deficiency type 9', 'combined oxidative phosphorylation deficiency caused by mutation in MRPL3']",0111472,614582,319509,C3281234,"['-0.652', '0.2725', '-0.005463', '-0.2299', '0.2136', '-0.8247', '0.06323', '0.973', '-0.2966', '0.493', '-0.3953', '-0.3662', '0.619', '-0.567', '-0.1482', '-0.00867', '0.527', '-0.2922', '-0.3618', '-0.9297', '0.4407', '-0.2964', '0.744', '0.2211', '0.018', '-0.199', '0.3354', '0.1697', '-0.4343', '-0.1045', '0.4656', '0.721', '0.932', '-0.1654', '-0.3538', '-0.535', '0.1143', '0.0314', '0.009056', '-0.3547', '-0.2954', '0.04782', '0.09644', '0.685', '-0.7744', '-0.2607', '0.05072', '0.0252', '0.01477', '0.289', '-0.3997', '-0.375', '-0.146', '0.07587', '-0.1896', '-0.1892', '0.3313', '0.05704', '-0.3232', '0.653', '0.08344', '0.4011', '0.534', '-0.0947', '-0.2983', '-0.1769', '0.3938', '0.3386', '-0.4175', '0.2605', '-0.3203', '0.3745', '0.0765', '-0.1781', '0.2732', '-0.1426', '0.2242', '-0.09106', '-0.3237', '0.5776', '0.303', '0.079', '-0.02252', '-0.2487', '-0.3914', '0.0643', '0.2913', '0.514', '0.5864', '-0.042', '0.1989', '-0.133', '-0.3508', '0.2805', '0.4023', '0.6753', '0.02057', '-0.3977', '0.06134', '0.0331']",,,,,,,
mondo:0013812,Baraitser-winter syndrome 2,"['Baraitser-Winter cerebrofrontofacial syndrome caused by mutation in ACTG1', 'Baraitser-Winter syndrome type 2', 'ACTG1 Baraitser-Winter cerebrofrontofacial syndrome', 'Baraitser-winter syndrome 2', 'Baraitser-WINTER syndrome 2', 'BRWS2']",0081113,614583,,C3281235,,,,,,,,
mondo:0013813,dystonia 21,"['DYT21', 'primary dystonia, DYT21 type', 'dystonia 21', 'dystonia type 21']",0090046,614588,306734,C3281236,,,,,,,,
mondo:0013814,"podoconiosis, susceptibility to","['Nonfilarial elephantiasis of Lower legs, susceptibility to', 'PDCOS', 'lymphostatic verrucosis, susceptibility to', 'endemic Nonfilarial elephantiasis, susceptibility to', 'podoconiosis, susceptibility to']",,614590,,,,,,,,,,
mondo:0013815,bent bone dysplasia syndrome 1,"['FGFR2-related bent bone dysplasia', 'perinatal lethal bent bone dysplasia', 'bent bone dysplasia (BBD)-FGFR2 type', 'BBDS', 'bent bone dysplasia syndrome']",,614592,313855,C3281247,"['-0.4604', '0.179', '0.4592', '-0.3774', '0.2927', '-0.1121', '-0.1838', '0.4983', '-0.2986', '-0.09424', '-0.175', '-0.05664', '0.01791', '-0.12177', '-0.344', '0.1315', '0.3352', '-0.1106', '-0.2673', '-0.4126', '0.0363', '-0.0649', '0.3901', '-0.2568', '0.2534', '0.1287', '-0.0764', '-0.02039', '0.4595', '-0.3528', '0.0944', '-0.2158', '0.2627', '0.1526', '0.3533', '-0.2179', '-0.0691', '-0.2534', '-0.0975', '-0.651', '-0.1478', '0.05316', '0.009155', '-0.3503', '-0.2214', '-0.3486', '0.0793', '0.443', '0.2583', '0.0716', '-0.0857', '-0.257', '0.1548', '0.3704', '-0.5073', '-0.4617', '-0.02226', '-0.08685', '-0.2277', '0.287', '0.4075', '0.2174', '-0.4045', '0.03925', '0.0348', '-0.0926', '0.205', '0.2952', '-0.08636', '0.3367', '-0.2937', '0.0741', '0.3147', '-0.05356', '-0.4036', '-0.02722', '0.2219', '-0.010666', '-0.2355', '-0.223', '0.00623', '0.09283', '-0.03534', '0.1978', '-0.3071', '0.01581', '-0.1099', '0.2206', '0.2051', '0.0734', '-0.3333', '0.1302', '0.1626', '0.0943', '0.3918', '0.1261', '0.6724', '-0.444', '0.3313', '0.06226']",,,,,,,
mondo:0013817,preeclampsia/eclampsia 5,"['CORIN preeclampsia', 'PREECLAMPSIA/eclampsia 5', 'PEE5', 'preeclampsia/eclampsia 5', 'Preeclampsia/eclampsia type 5', 'Corin preeclampsia', 'preeclampsia caused by mutation in Corin']",,614595,,C3281288,,,,,,,,
mondo:0013818,trichohepatoenteric syndrome 2,"['Trichohepatoenteric syndrome 2', 'Trichohepatoenteric syndrome type 2', 'THES2', 'TRICHOHEPATOENTERIC syndrome 2', 'tricho-hepato-enteric syndrome caused by mutation in SKIV2L', 'SKIV2L tricho-hepato-enteric syndrome']",0111416,614602,,C3281289,,,,,,,,
mondo:0013819,"intellectual disability, autosomal dominant 14","['mental retardation, autosomal dominant 14', 'MRD14', 'Coffin-Siris syndrome 2', 'intellectual disability, autosomal dominant 14', 'CSS2', 'Coffin-Siris syndrome caused by mutation in ARID1A', 'autosomal dominant intellectual disability 14', 'COFFIN-SIRIS syndrome 2', 'ARID1A-related BAFopathy', 'intellectual disability, autosomal dominant type 14', 'autosomal dominant mental retardation 14', 'ARID1A Coffin-Siris syndrome', 'mental retardation, autosomal dominant type 14']",0070044,614607,,C3553247,,,,,,,,
mondo:0013820,"intellectual disability, autosomal dominant 15","['autosomal dominant mental retardation 15', 'intellectual disability, autosomal dominant 15', 'Coffin-Siris syndrome caused by mutation in SMARCB1', 'SMARCB1-related BAFopathy', 'intellectual disability, autosomal dominant type 15', 'autosomal dominant intellectual disability 15', 'SMARCB1 Coffin-Siris syndrome', 'mental retardation, autosomal dominant type 15', 'CSS3', 'COFFIN-SIRIS syndrome 3', 'MRD15', 'mental retardation, autosomal dominant 15']",0070045,614608,,C3553248,,,,,,,,
mondo:0013821,"intellectual disability, autosomal dominant 16","['MRD16', 'autosomal dominant mental retardation 16', 'autosomal dominant intellectual disability 16', 'mental retardation, autosomal dominant type 16', 'Coffin-Siris syndrome caused by mutation in SMARCA4', 'SMARCA4-related BAFopathy', 'intellectual disability, autosomal dominant 16', 'mental retardation, autosomal dominant 16', 'COFFIN-SIRIS syndrome 4', 'intellectual disability, autosomal dominant type 16', 'CSS4', 'SMARCA4 Coffin-Siris syndrome']",0070046,614609,,C3553249,,,,,,,,
mondo:0013822,acrodysostosis 2 with or without hormone resistance,"['acrodysostosis 2, with or without hormone resistance', 'acrodysostosis 2 with or without hormone resistance', 'acrodysostosis caused by mutation in PDE4D', 'ACRDYS2', 'PDE4D acrodysostosis']",,614613,,C3553250,,,,,,,,
mondo:0013823,autosomal dominant nonsyndromic hearing loss 4B,"['deafness, autosomal dominant 4B', 'deafness, autosomal dominant type 4B', 'autosomal dominant deafness 4B', 'CEACAM16 autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness type 4B', 'deafness, autosomal dominant 4b', 'autosomal dominant nonsyndromic deafness 4B', 'DFNA4B', 'autosomal dominant nonsyndromic deafness caused by mutation in CEACAM16']",0110574,614614,,C3281297,,,,,,,,
mondo:0013824,Joubert syndrome 17,"['JBTS17', 'Joubert syndrome 17', 'Joubert syndrome caused by mutation in CPLANE1', 'Joubert syndrome type 17', 'CPLANE1 Joubert syndrome']",0110986,614615,,C3553264,"['-0.0153', '0.01883', '-0.004494', '-0.00972', '0.004517', '-0.02779', '-0.000465', '0.0297', '-0.02646', '-0.03162', '-0.01219', '-0.01518', '-0.009285', '0.0002184', '-0.00364', '-0.008354', '0.013405', '-0.0161', '-0.01181', '-0.067', '-0.01985', '-0.007156', '0.02187', '-0.02184', '0.00984', '-0.01572', '-0.01772', '-0.018', '0.005543', '-0.0171', '0.03046', '0.02008', '0.04446', '0.003044', '0.01453', '-0.00903', '-0.01351', '-0.01955', '-0.001312', '-0.01843', '0.01425', '-0.02557', '-0.0014515', '-0.0073', '-9.5e-06', '-0.03848', '-0.01293', '0.02672', '0.01048', '0.006348', '-0.0156', '0.002056', '0.003567', '-0.002424', '-0.0217', '-0.010735', '0.0308', '-0.00923', '-0.0415', '0.003033', '0.013725', '0.01146', '-0.0013075', '4.3e-06', '0.006775', '0.00799', '0.03275', '0.01877', '-0.0407', '0.04407', '-0.0308', '0.0064', '4.35e-05', '-0.01662', '0.02516', '0.02747', '0.007458', '0.001685', '-0.02673', '-0.003143', '0.005287', '-0.000902', '-0.005463', '0.02127', '-0.01697', '-0.008224', '0.02666', '0.03296', '0.04248', '-0.003172', '0.01503', '0.02985', '0.002487', '0.006256', '0.0516', '0.014206', '0.036', '-0.03384', '-0.01208', '0.014015']",C175702,,,,,,
mondo:0013825,congenital diarrhea 6,"['diarrhea type 6', 'GUCY2C congenital diarrhoea', 'congenital diarrhoea type 6', 'congenital diarrhoea caused by mutation in GUCY2C', 'diarrhoea 6', 'chronic diarrhoea due to guanylate cyclase 2C overactivity', 'congenital diarrhea caused by mutation in GUCY2C', 'congenital diarrhea type 6', 'chronic diarrhea due to guanylate cyclase 2C overactivity', 'DIAR6', 'diarrhea 6', 'GUCY2C congenital diarrhea', 'diarrhoea type 6']",0060780,614616,314373,C3553270,"['0.2341', '0.2029', '0.543', '0.405', '-0.3586', '-0.792', '-1.049', '0.3538', '-0.06323', '0.01084', '0.7676', '0.5156', '0.3218', '0.892', '-1.176', '0.0614', '-0.321', '0.1616', '-0.7295', '-0.9614', '-0.03912', '-0.1881', '-0.3674', '-0.0416', '0.06494', '-0.5146', '-0.7783', '0.4604', '0.5767', '-0.9277', '-0.4138', '-0.4253', '-0.05453', '0.3875', '1.083', '0.5713', '-0.4885', '0.2462', '0.1605', '-0.01863', '-0.4602', '-0.644', '-0.4692', '-0.5293', '0.4766', '-0.01804', '-0.0673', '0.3508', '-0.09235', '1.082', '-0.733', '-0.1747', '0.2074', '-0.4243', '0.05148', '-0.3398', '-0.1776', '-0.0854', '-0.8003', '-0.0887', '0.6875', '0.7295', '0.5713', '-0.5474', '0.0717', '-0.13', '0.3909', '-0.28', '0.364', '0.949', '-0.3516', '0.729', '0.1543', '-0.773', '0.7363', '0.2178', '-0.5874', '0.2233', '0.10266', '0.6636', '-0.2527', '-0.785', '-0.165', '0.04135', '0.343', '0.391', '0.6597', '0.2664', '0.05948', '-0.448', '-0.1976', '-0.2184', '-0.4216', '-0.5625', '0.653', '0.7114', '0.3752', '-1.619', '-0.2788', '-0.2617']",,,,,,,
mondo:0013826,autosomal recessive nonsyndromic hearing loss 86,"['DFNB86', 'deafness, autosomal recessive 86', 'autosomal recessive nonsyndromic deafness type 86', 'autosomal recessive nonsyndromic deafness 86', 'TBC1D24 autosomal recessive nonsyndromic deafness', 'autosomal recessive deafness 86', 'autosomal recessive nonsyndromic deafness caused by mutation in TBC1D24', 'deafness, autosomal recessive type 86']",0110532,614617,,C2829265,,,,,,,,
mondo:0013827,hyperekplexia 3,"['hyperekplexia type 3', 'SLC6A5 hereditary hyperekplexia', 'hyperekplexia 3', 'hereditary hyperekplexia caused by mutation in SLC6A5', 'HKPX3']",0060698,614618,,C3553288,,,,,,,,
mondo:0013828,hyperekplexia 2,"['hyperekplexia 2', 'HKPX2', 'GLRB hereditary hyperekplexia', 'hyperekplexia type 2', 'hereditary hyperekplexia caused by mutation in GLRB']",0060697,614619,,C3553291,,,,,,,,
mondo:0013829,UV-sensitive syndrome 2,"['UV-sensitive syndrome type 2', 'UV-sensitive syndrome caused by mutation in ERCC8', 'UVSS2', 'UV-sensitive syndrome 2', 'ERCC8 UV-sensitive syndrome']",,614621,,C3553298,,C173110,,,,,,
mondo:0013830,keratoconus 5,"['KTCN5', 'keratoconus 5']",,614622,,C3553302,,,,,,,,
mondo:0013831,keratoconus 6,"['keratoconus 6', 'KTCN6']",,614623,,C3553306,,,,,,,,
mondo:0013832,keratoconus 8,"['keratoconus 8', 'KTCN8']",,614628,,C3553307,,,,,,,,
mondo:0013833,keratoconus 7,"['KTCN7', 'keratoconus 7']",,614629,,C3553308,,,,,,,,
mondo:0013834,UV-sensitive syndrome 3,"['UVSSA UV-sensitive syndrome', 'UV-sensitive syndrome 3', 'UVSS3', 'UV-sensitive syndrome caused by mutation in UVSSA', 'UV-sensitive syndrome type 3']",,614640,,C3553328,,C173107,,,,,,
mondo:0013835,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7","['muscular dystrophy-dystroglycanopathy, type A caused by mutation in ISPD', 'Walker-Warburg syndrome or muscle-eye-brain disease, ISPD-related', 'ISPD muscular dystrophy-dystroglycanopathy, type A', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 7', 'MDDGA7', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 7']",0111234,614643,899,C3553330,,,,,,,,
mondo:0013836,familial steroid-resistant nephrotic syndrome with sensorineural deafness,"['coenzyme Q10 deficiency, primary, type 6', 'COQ10D6', 'coenzyme Q10 deficiency, primary, 6']",0070243,614650,280406,C3553349,"['0.631', '-0.2742', '0.05234', '0.0996', '-0.5806', '-0.2815', '0.2825', '0.239', '-0.544', '-0.3748', '0.28', '-0.03998', '-0.762', '0.745', '-0.552', '-0.0644', '-0.02222', '0.667', '0.514', '-0.652', '0.846', '-0.716', '0.1833', '0.596', '0.1493', '-0.2712', '-0.758', '0.0997', '0.1346', '-0.4314', '0.782', '-0.11456', '1.047', '0.02818', '-0.5054', '-0.3357', '-0.0752', '0.1692', '0.1958', '-0.502', '-0.1676', '0.4111', '-0.4714', '-0.4941', '0.03029', '-0.2583', '0.248', '-0.004227', '0.2944', '-0.68', '-0.3105', '0.683', '1.308', '-0.53', '-0.175', '-0.6924', '0.09985', '0.1115', '-1.129', '-0.0909', '-0.4104', '-0.4866', '0.11554', '-0.634', '-0.2832', '-0.10114', '0.6025', '0.2595', '-0.8174', '0.4863', '-0.544', '0.6685', '0.4756', '-0.18', '0.2844', '0.02559', '0.361', '1.101', '-0.1167', '0.4492', '-0.05606', '-0.1396', '-0.1986', '-0.1305', '-0.1663', '-0.3503', '-0.1444', '-0.1617', '0.329', '0.5776', '0.8096', '0.7744', '-0.675', '-0.257', '0.3135', '0.6006', '-0.4277', '-0.7793', '-0.1481', '-0.1915']",,,,,,,
mondo:0013837,deafness-encephaloneuropathy-obesity-valvulopathy syndrome,"['hearing loss-encephaloneuropathy-obesity-valvulopathy syndrome', 'coenzyme Q10 deficiency, primary, 2', 'COQ10D2', 'coenzyme Q10 deficiency, primary, type 2']",0070239,614651,254898,C3553354,"['0.0469', '0.5786', '0.002176', '0.8335', '-0.2961', '-0.759', '0.1193', '0.7046', '-0.0644', '-0.4807', '-0.11316', '0.4082', '0.2313', '0.1271', '-0.9604', '-0.4688', '-0.2418', '1.054', '-0.628', '-0.7134', '0.03986', '-0.3882', '0.2593', '-0.3005', '-0.1123', '0.2164', '-0.4827', '-0.519', '0.308', '-0.2522', '0.34', '-0.6562', '0.4133', '0.007294', '-0.1971', '-0.5557', '-0.863', '0.105', '0.4639', '0.1753', '0.02892', '-0.2429', '-0.6924', '0.447', '-0.04657', '-0.6836', '0.521', '0.0917', '0.1757', '0.114', '-0.5015', '0.04175', '0.4631', '-0.3647', '-0.1545', '0.5156', '-0.2766', '-0.115', '-0.001946', '-0.2313', '0.546', '0.3376', '-0.301', '-0.5654', '-0.2979', '0.643', '-0.4922', '0.407', '0.4849', '0.721', '0.06107', '0.6787', '-0.01785', '-0.1271', '0.3923', '-0.6445', '-0.0638', '0.04636', '-1.216', '0.617', '0.05353', '1.065', '0.02948', '0.291', '1.001', '0.744', '0.323', '0.2605', '0.7324', '0.489', '-0.09515', '0.3325', '-0.2144', '0.4614', '0.7373', '0.12384', '0.2698', '-0.279', '-0.3604', '-0.01654']",,,,,,,
mondo:0013838,"coenzyme Q10 deficiency, primary, 3","['PDSS2 coenzyme Q10 deficiency', 'COQ10D3', 'coenzyme Q10 deficiency, primary, 3', 'coenzyme Q10 deficiency, primary, type 3', 'coenzyme Q10 deficiency caused by mutation in PDSS2']",0070240,614652,,C3553358,,,,,,,,
mondo:0013839,hereditary sensory and autonomic neuropathy type 6,"['familial dysautonomia with contractures', 'HSAN 6', 'hereditary sensory and autonomic neuropathy caused by mutation in DST', 'hereditary sensory and autonomic neuropathy type VI', 'neuropathy, hereditary sensory and autonomic, type 6', 'HSAN6', 'DST hereditary sensory and autonomic neuropathy', 'neuropathy, hereditary sensory and autonomic, type VI']",0070151,614653,314381,C3539003,"['0.8174', '-0.1197', '-0.4202', '0.7134', '-0.365', '-0.623', '-0.1065', '0.2908', '-0.786', '0.308', '0.1004', '0.7837', '0.02853', '0.854', '-0.7036', '0.3535', '-0.0807', '0.7183', '-0.959', '-0.8184', '0.4395', '-0.003078', '-0.8096', '0.4739', '0.2368', '-0.1775', '-0.5137', '-0.03165', '-0.2288', '-0.38', '0.8057', '0.2318', '0.2812', '-0.1307', '-0.301', '-0.368', '0.02171', '0.0949', '0.04517', '-0.4597', '-0.4907', '0.1528', '0.10046', '-0.03632', '0.3462', '-0.427', '0.5146', '-0.08374', '0.417', '-0.02165', '-0.507', '1.076', '0.1311', '-0.795', '-0.1552', '0.7188', '0.716', '0.2173', '-0.4558', '-0.5415', '0.4229', '0.804', '0.3733', '0.331', '-0.1721', '0.771', '0.3953', '0.4812', '-0.0331', '0.2318', '-0.74', '0.471', '-0.4675', '-0.2502', '0.725', '0.01654', '-0.04437', '0.845', '-0.6367', '0.5464', '0.01044', '-0.724', '0.383', '0.2913', '-0.00574', '-0.3513', '0.1625', '0.1583', '0.857', '-0.416', '0.2751', '-0.2435', '0.8022', '-0.2067', '1.112', '1.01', '-0.484', '-0.164', '0.1766', '0.2281']",,,,,,,
mondo:0013840,encephalopathy-hypertrophic cardiomyopathy-renal tubular disease syndrome,"['coenzyme Q10 deficiency, primary, type 5', 'COQ10D5', 'coenzyme Q10 deficiency, primary, 5']",0070242,614654,319678,C3553374,"['0.1149', '-0.3838', '0.02518', '0.5415', '-0.0904', '-0.1622', '0.3657', '0.512', '-0.2134', '-0.398', '0.1565', '-0.589', '-0.3198', '0.0559', '-0.459', '0.2242', '-0.592', '-0.1902', '-0.664', '-0.883', '0.2451', '0.0165', '0.5283', '0.128', '0.4294', '-0.4482', '0.1624', '0.394', '-0.1322', '-0.2803', '0.5654', '-0.1335', '0.81', '-0.005337', '0.1652', '-0.4548', '-0.146', '-0.4749', '0.7544', '-0.2766', '0.1356', '0.394', '-0.10004', '0.4834', '0.446', '0.265', '0.2379', '0.787', '0.2333', '-0.5474', '-0.4646', '0.0837', '0.3235', '-0.1567', '0.3286', '-0.3752', '-0.3867', '0.5215', '-0.8135', '0.2396', '0.01683', '0.4685', '0.2524', '-0.979', '-1.043', '0.2336', '0.1346', '0.541', '-0.835', '-0.2133', '-0.2969', '0.4949', '-0.05466', '-0.1256', '-0.1759', '0.362', '0.1919', '-0.2206', '-0.2068', '0.3953', '-0.07574', '0.07715', '0.0988', '-0.447', '0.932', '-0.04547', '0.623', '-0.0131', '0.4355', '0.1986', '0.5537', '0.05765', '-0.2058', '0.05154', '0.822', '0.931', '0.1583', '-0.2275', '-0.09534', '-0.2003']",,,,,,,
mondo:0013841,"stuttering, familial persistent, 3","['stuttering, familial persistent, 3', 'STUT3']",,614655,,C3553381,,,,,,,,
mondo:0013842,cortisone reductase deficiency 2,"['cortisone reductase deficiency type 2', 'cortisone reductase deficiency caused by mutation in HSD11B1', '11-beta-hydroxysteroid dehydrogenase type 1 deficiency', 'HSD11B1 cortisone reductase deficiency', 'CORTRD2', 'cortisone reductase deficiency 2']",0090140,614662,,C3553382,,C131084,,,,,,
mondo:0013843,intestinal obstruction in the newborn due to guanylate cyclase 2C deficiency,"['meconium ileus', 'GUCY2C meconium ileus', 'meconium ileus due to guanylate cyclase 2C deficiency']",,614665,314376,,"['-0.6353', '0.2346', '-0.3167', '-0.0669', '-0.2124', '-0.3894', '-0.1812', '-0.00975', '-0.2274', '0.1288', '-0.1588', '-0.4583', '-0.01271', '0.3616', '-0.3218', '-0.1559', '-0.8564', '0.1727', '-0.9883', '-1.089', '-0.1542', '0.01533', '-0.2218', '-0.4038', '0.597', '0.2426', '-0.2288', '1.429', '0.7935', '-0.1992', '0.1423', '-0.372', '0.1705', '0.1721', '0.2073', '0.08685', '-0.0908', '-0.2188', '-0.06866', '0.568', '-0.3652', '-0.7515', '0.202', '0.0534', '0.418', '-0.01366', '-0.0175', '-0.4382', '-0.0812', '0.2385', '-0.03918', '-0.069', '0.3765', '-0.2059', '0.1743', '-0.6562', '-0.1735', '0.1992', '-0.347', '-0.1422', '0.02237', '0.749', '0.4607', '-0.10516', '-0.2042', '0.627', '0.454', '0.0415', '0.02887', '-0.2869', '-0.06836', '0.3896', '0.0634', '-0.177', '0.05167', '0.2458', '-0.01511', '0.827', '-0.00859', '0.3652', '-0.5693', '-0.2137', '0.053', '-0.3193', '0.1304', '0.2191', '1.118', '0.4302', '0.3406', '-1.045', '-0.11536', '0.4517', '-0.4458', '0.002186', '1.222', '-0.004032', '0.3013', '-0.2491', '0.3901', '0.5044']",,,,777.1,,,
mondo:0013844,"stuttering, familial persistent, 4","['stuttering, familial persistent, 4', 'STUT4']",,614668,,C3553403,,,,,,,,
mondo:0013845,auriculocondylar syndrome 2,"['auriculocondylar syndrome caused by mutation in PLCB4', 'PLCB4 auriculocondylar syndrome', 'Auriculocondylar syndrome 2', 'AURICULOCONDYLAR syndrome 2', 'Auriculocondylar syndrome type 2', 'ARCND2']",,614669,,C3553404,,,,,,,,
mondo:0013846,"peripartum cardiomyopathy, susceptibility to","['Ppcm, susceptibility to', 'peripartum cardiomyopathy, susceptibility to']",,614670,,,,,,,,,,
mondo:0013847,chromosome 16p11.2 duplication syndrome,"['chromosome 16p11.2 duplication syndrome', 'susceptibility to autism, 14B', '16p11.2 duplication syndrome', '16p11.2 microduplication', 'autism, susceptibility to, 14B', 'proximal trisomy 16p11.2', 'proximal 16p11.2 microduplication syndrome', 'AUTS14B', '16p11.2 duplication', 'proximal dup(16)(p11.2)']",0060430,614671,370079,C3553407,,,,,,,,
mondo:0013848,dilated cardiomyopathy 2B,"['cardiomyopathy, dilated, type 2B', 'CMD2B', 'GATAD1 familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 2B', 'cardiomyopathy, dilated, 2B', 'familial isolated dilated cardiomyopathy caused by mutation in GATAD1']",0110441,614672,,C3553409,,,,,,,,
mondo:0013849,"microcephaly 8, primary, autosomal recessive","['MCPH8', 'microcephaly 8, primary, autosomal recessive', 'CEP135 autosomal recessive primary microcephaly', 'autosomal recessive primary microcephaly caused by mutation in CEP135']",0070282,614673,,C3553414,,,,,,,,
mondo:0013851,autosomal dominant aplasia and myelodysplasia,"['autosomal dominant aplastic anaemia and myelodysplasia', 'bone marrow failure syndrome type 1', 'autosomal dominant aplastic anemia and myelodysplasia', 'BMFS1', 'bone marrow failure syndrome 1']",,614675,314399,CN203751,"['-0.05405', '0.1015', '0.15', '-0.4106', '0.3105', '-0.104', '-0.1958', '0.2041', '-0.2136', '-0.3235', '-0.002478', '0.2817', '-0.12067', '-0.1342', '0.04684', '-0.3296', '0.1545', '-0.082', '0.05524', '-0.5264', '-0.1665', '-0.2937', '0.1105', '-0.3835', '0.1527', '-0.1134', '0.1059', '-0.1505', '0.2466', '-0.2499', '0.05795', '0.0911', '0.3472', '0.212', '0.04764', '-0.04343', '-0.4417', '-0.4268', '-0.1907', '-0.1157', '-0.0725', '-0.04025', '0.2054', '-0.1718', '-0.2864', '-0.568', '-0.2744', '0.2493', '0.107', '-0.09045', '0.03085', '0.09924', '0.12494', '-0.02843', '0.1346', '-0.398', '-0.05695', '-0.072', '-0.541', '0.0529', '0.2372', '0.11316', '-0.01758', '-0.3704', '0.1389', '-0.2269', '0.5303', '0.3381', '-0.2803', '0.3516', '-0.3179', '-0.2136', '0.0343', '-0.2634', '0.1459', '-0.2766', '0.0831', '0.04117', '0.03128', '-0.1945', '-0.0255', '0.007812', '0.1583', '-0.03943', '0.11194', '-0.1389', '0.247', '0.3196', '0.1256', '0.2174', '0.284', '0.1786', '0.1144', '-0.1942', '0.3108', '0.433', '0.5', '-0.1658', '0.2515', '0.03998']",,,,,,,
mondo:0013852,hypertrophic cardiomyopathy 21,"['CMH21', 'cardiomyopathy, hypertrophic, 21', 'cardiomyopathy familial hypertrophic 21', 'hypertrophic cardiomyopathy type 21', 'cardiomyopathy, familial hypertrophic, 21']",0110311,614676,,C3553442,,,,,,,,
mondo:0013853,pontocerebellar hypoplasia type 1B,"['PCH1B', 'EXOSC3 non-syndromic pontocerebellar hypoplasia', 'non-syndromic pontocerebellar hypoplasia caused by mutation in EXOSC3', 'pontocerebellar hypoplasia, type 1B']",0060266,614678,,C3553449,,,,,,,,
mondo:0013854,primary ciliary dyskinesia 17,"['primary ciliary dyskinesia 17 with or without situs inversus', 'primary ciliary dyskinesia type 17', 'ciliary dyskinesia, primary, 17', 'ciliary dyskinesia, primary, type 17', 'CILD17', 'primary ciliary dyskinesia caused by mutation in CCDC103', 'ciliary dyskinesia, primary, 17, with or without situs inversus', 'CCDC103 primary ciliary dyskinesia']",0110621,614679,,C3542550,,,,,,,,
mondo:0013855,"influenza, severe, susceptibility to","['influenza, severe, susceptibility to', 'susceptibility to severe influenza']",,614680,,,,,,,,,,
mondo:0013856,"hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes","['hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, mental retardation, and recurrent inflammatory episodes', 'hypertelorism and other facial dysmorphism, brachydactyly, genital abnormalities, intellectual disability, and recurrent inflammatory episodes']",,614684,,C3553465,,,,,,,,
mondo:0013857,"alar cleft, isolated","['alar cleft, isolated']",,614687,,C3553476,,,,,,,,
mondo:0013858,pontine tegmental cap dysplasia,"['PONTINE tegmental CAP dysplasia', 'pontine tegmental cap dysplasia', 'PTCD']",,614688,269229,C3541340,,,,,,,,
mondo:0013859,cataract 38,"['cataract type 38', 'AGK early-onset non-syndromic cataract', 'cataract 38', 'early-onset non-syndromic cataract caused by mutation in AGK', 'CTRCT38', 'cataract 38, autosomal recessive', 'CATC5', 'autosomal recessive congenital cataract 5', 'cataract, autosomal recessive congenital 5']",0110245,614691,,C3553494,,,,,,,,
mondo:0013860,idiopathic membranous glomerulonephritis,"['Extramembranous glomerulonephritis', 'MGN', 'membranous nephropathy, susceptibility to', 'membranous GN', 'glomerulonephritis, membranous', 'membranous nephropathy - Idiopathic', 'Idiopathic membranous glomerulopathy', 'idiopathic membranous nephropathy', 'MBNP']",,614692,97560,C0086445,,C123060,,,,,,
mondo:0013862,"immunodeficiency, common variable, 7","['immunodeficiency, common variable, 7', 'immunodeficiency, common variable, type 7', 'CVID7']",0081150,614699,,C3542922,,,,,,,,
mondo:0013863,combined immunodeficiency due to LRBA deficiency,"['immunodeficiency, common variable, 8, with autoimmunity', 'CVID8', 'CID due to LRBA deficiency']",0081151,614700,445018,C3553512,,,,,,,,
mondo:0013864,Cornelia de Lange syndrome 4,"['Cornelia DE Lange syndrome 4', 'Cornelia de Lange syndrome caused by mutation in RAD21', 'RAD21 Cornelia de Lange syndrome', 'CDLS4', 'Cornelia de Lange syndrome 4', 'Cornelia De Lange syndrome type 4']",0080508,614701,,C3553517,,,,,,,,
mondo:0013865,mitochondrial hypertrophic cardiomyopathy with lactic acidosis due to MTO1 deficiency,"['combined oxidative phosphorylation deficiency caused by mutation in MTO1', 'cardiomyopathy, infantile hypertrophic mitochondrial, and lactic acidosis', 'combined oxidative phosphorylation deficiency type 10', 'combined oxidative phosphorylation deficiency 10', 'combined oxidative phosphorylation defect type 10', 'MTO1 combined oxidative phosphorylation deficiency', 'COXPD10']",0111480,614702,314637,C3553529,"['-0.03543', '-0.2252', '-0.1145', '1.155', '-0.03845', '-0.12225', '0.269', '1.49', '-0.2515', '-0.1875', '0.5947', '-0.659', '-0.2179', '0.3396', '-0.5815', '-0.6636', '-0.8257', '-0.7124', '-0.9604', '-0.8325', '0.38', '-0.02353', '0.2124', '0.4065', '-0.1843', '-0.2388', '-0.04086', '0.436', '0.3447', '0.3145', '0.741', '-0.09576', '0.601', '0.1461', '-0.4614', '0.06232', '0.0475', '-0.0566', '0.2063', '-0.5645', '0.544', '-0.07904', '0.1794', '0.4175', '0.1265', '0.0983', '-0.6045', '0.2363', '-0.12146', '-0.2312', '-0.2168', '-0.0472', '-0.1074', '0.5054', '0.3574', '-0.639', '-0.6772', '1.134', '0.0512', '-0.4043', '-0.2021', '0.3362', '0.6616', '-0.2354', '-0.4382', '-0.012245', '0.1112', '0.5503', '-0.4233', '0.6978', '0.1219', '0.488', '0.8315', '-0.4238', '-0.4207', '0.08044', '-0.04306', '-0.1443', '0.0745', '0.9326', '0.7734', '-0.337', '-0.008545', '-0.246', '0.6953', '-0.2595', '0.501', '0.187', '0.817', '0.582', '0.27', '-0.2137', '-0.7144', '0.255', '0.6167', '0.783', '0.2434', '0.01941', '-0.4407', '0.1774']",,,,,,,
mondo:0013866,neuronal ceroid lipofuscinosis 11,"['GRN neuronal ceroid lipofuscinosis', 'ceroid lipofuscinosis, neuronal, type 11', 'Grn neuronal ceroid lipofuscinosis', 'CLN11 disease', 'neuronal ceroid lipofuscinosis caused by mutation in Grn', 'ceroid lipofuscinosis, neuronal, 11', 'neuronal ceroid lipofuscinosis type 11', 'CLN11']",0110732,614706,314629,C3539123,"['-0.3042', '0.3884', '-0.0896', '0.2468', '0.0321', '-0.4136', '-0.159', '-0.094', '-0.212', '-0.01758', '-0.1294', '0.0381', '-0.1018', '-0.0699', '0.1498', '-0.2583', '-0.0817', '-0.0837', '-0.0729', '-0.3218', '0.2225', '-0.2578', '0.08984', '-0.1', '0.05', '-0.0636', '-0.03595', '-0.0448', '-0.2527', '0.1251', '0.1647', '0.1021', '0.2147', '0.05737', '0.3823', '0.03098', '0.05237', '-0.2181', '-0.02574', '-0.2463', '0.05792', '-0.3826', '0.134', '0.01608', '-0.2294', '-0.4873', '0.0841', '0.1902', '0.2194', '0.2026', '0.2225', '-0.05585', '-0.08575', '0.01991', '-0.05862', '-0.616', '0.4783', '-0.026', '-0.499', '0.12476', '0.2494', '0.06305', '0.1824', '0.06396', '-0.003609', '0.0917', '0.4175', '0.0665', '-0.2047', '0.182', '-0.2112', '-0.0681', '0.0684', '-0.1965', '0.1014', '0.0365', '-0.0288', '0.2142', '-0.222', '-0.0281', '0.0938', '-0.257', '-0.09393', '0.344', '0.005768', '-0.4485', '0.2042', '0.255', '0.0823', '0.1888', '0.2886', '-0.03732', '-0.01976', '-0.00962', '0.3018', '0.187', '0.567', '-0.3171', '-0.04532', '-0.05148']",,,,,,,
mondo:0013867,brown-Vialetto-van Laere syndrome 2,"['Brown-Vialetto-van Laere syndrome caused by mutation in SLC52A2', 'brown-Vialetto-van Laere syndrome 2', 'Brown-Vialetto-Van Laere syndrome type 2', 'BROWN-Vialetto-VAN Laere syndrome 2', 'BVVLS2', 'SLC52A2 Brown-Vialetto-van Laere syndrome']",0080786,614707,572550,C3553538,,C183529,,,,,,
mondo:0013868,"porokeratosis 7, multiple types","['porokeratosis 7, disseminated superficial actinic type', 'POROK7', 'porokeratosis 7, multiple types']",,614714,,,,,,,,,,
mondo:0013869,adenine phosphoribosyltransferase deficiency,"['nephrolithiasis, Dha', '2,8-dihydroxyadeninuria disease', 'urolithiasis, 2,8-dihydroxyadenine', '2,8-dihydroxyadenine urolithiasis', 'urolithiasis, Dha', 'APRTD', 'Dihydroxyadeninuria', 'adenine phosphoribosyltransferase deficiency', 'APRT deficiency']",0060350,614723,976,C0268120,"['0.392', '0.09375', '-0.6807', '0.2815', '0.005054', '-0.3457', '0.1619', '0.999', '0.1941', '0.118', '0.273', '-0.7437', '-0.3936', '0.5093', '0.013054', '-0.3684', '-0.298', '-0.0409', '0.3179', '-0.889', '-0.5254', '-0.4922', '1.09', '0.07166', '0.00272', '0.2288', '-0.612', '0.1193', '-0.2229', '0.3906', '0.5615', '-0.4268', '0.2106', '0.437', '-0.2319', '-0.4385', '0.2935', '-0.1571', '0.204', '0.1172', '-0.2693', '-0.2484', '0.8535', '-0.2505', '0.3108', '-0.1802', '-0.5986', '-0.6367', '0.3645', '1.035', '-0.0956', '-0.3809', '0.4514', '-0.4531', '0.3364', '-0.3062', '0.911', '0.08936', '-0.5244', '0.478', '0.4001', '0.1503', '-0.013374', '-0.4426', '0.4553', '-0.5815', '0.3174', '0.5376', '0.1008', '-0.1676', '-0.1048', '-0.0478', '-0.482', '-0.002335', '0.516', '0.3088', '0.143', '0.3152', '-0.05643', '0.718', '-0.1654', '0.03836', '0.4753', '0.01886', '0.3074', '-0.02292', '0.2515', '-0.5244', '0.0758', '0.4546', '0.539', '0.764', '-0.6895', '-0.5454', '0.8003', '0.2393', '0.4414', '-0.8555', '-0.688', '0.2014']",C121564,,C538228,,,,
mondo:0013870,TMEM165-congenital disorder of glycosylation,"['congenital disorder of glycosylation type 2k', 'congenital disorder of glycosylation type IIk', 'CDG IIk', 'TMEM165-CDG (CDG-IIk)', 'CDG-IIk', 'congenital disorder of glycosylation, type IIk', 'carbohydrate deficient glycoprotein syndrome type IIk', 'TMEM165-CDG', 'CDG syndrome type IIk', 'CDG2K']",0070263,614727,314667,C3553571,"['-0.3457', '-0.008064', '0.6396', '-0.338', '0.261', '-0.4253', '-0.05518', '0.444', '-0.61', '-0.5073', '-0.2', '-0.196', '-0.2896', '-0.009', '-0.4993', '0.2158', '0.1447', '0.1207', '-0.497', '-0.4902', '0.3083', '0.02612', '0.08246', '0.06793', '0.3706', '0.02692', '-0.102', '0.1506', '0.5034', '-0.3638', '0.2896', '0.4211', '0.63', '0.3008', '0.00257', '-0.342', '-0.12427', '-0.0583', '-0.3403', '-0.465', '-0.004456', '-0.3245', '0.2003', '0.1812', '-0.09344', '-0.11774', '0.169', '0.518', '0.2117', '0.1785', '-0.2988', '0.05835', '0.05527', '0.0638', '-0.1407', '-0.5215', '-0.02547', '0.2522', '-0.05246', '0.1875', '0.3489', '-0.1233', '-0.2284', '0.03427', '0.1675', '-0.0777', '0.1161', '0.1287', '-0.301', '0.0505', '-0.4575', '0.4143', '0.4138', '0.062', '-0.1869', '-0.03723', '0.3564', '-0.00385', '-0.3125', '0.273', '-0.1886', '-0.1181', '-0.11584', '0.4153', '-0.2656', '0.1808', '0.1058', '0.407', '0.4094', '0.2766', '-0.4177', '0.4075', '0.1874', '0.1626', '0.39', '0.321', '0.507', '-0.2654', '0.351', '0.4753']",,,,,,,
mondo:0013871,Seckel syndrome 6,"['Seckel syndrome type 6', 'Seckel syndrome caused by mutation in CEP63', 'CEP63 Seckel syndrome', 'Seckel syndrome 6', 'SCKL6']",0070006,614728,,C3553582,,,,,,,,
mondo:0013872,"prostate cancer, hereditary, 2","['prostate cancer, hereditary, type 2', 'prostate cancer, hereditary, 2', 'ELAC2 familial prostate cancer', 'familial prostate cancer caused by mutation in ELAC2', 'prostate cancer, hereditary, 2, susceptibility to', 'HPC2']",,614731,,C3539120,,,,,,,,
mondo:0013873,IMAGe syndrome,"['IMAGe syndrome', 'intrauterine growth retardation, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital anomalies', 'intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, genital abnormalities', 'intrauterine growth retardation-metaphyseal dysplasia-adrenal hypoplasia congenita-genital anomalies syndrome', 'intrauterine growth retardation - metaphyseal dysplasia - adrenal hypoplasia congenita - genital anomalies']",0050885,614732,85173,C1846009,"['-0.485', '0.1443', '0.4092', '-0.687', '0.317', '-0.3115', '-0.4558', '0.6455', '-0.733', '-0.7173', '0.307', '0.0506', '-0.1649', '-0.01322', '-0.1732', '0.1242', '0.2157', '-0.11035', '-0.358', '-0.4783', '0.04245', '-0.3057', '0.2301', '-0.1307', '0.1062', '-0.1459', '-0.3706', '0.10065', '0.768', '-0.561', '0.3557', '-0.1108', '0.3152', '-0.03174', '0.06223', '0.11176', '-0.2054', '-0.2189', '-0.0728', '-0.04413', '-0.02902', '0.2417', '0.02597', '0.0169', '-0.1256', '-0.528', '0.1915', '0.2206', '-0.1967', '-0.0473', '0.484', '-0.45', '-0.374', '0.1367', '-0.1372', '-0.3008', '0.2253', '-0.3774', '-0.05493', '0.453', '0.23', '0.10895', '-0.6265', '0.01377', '0.3232', '-0.009766', '0.4448', '0.5938', '-0.5376', '0.1088', '-0.3684', '0.308', '0.508', '0.1946', '-0.005714', '0.11615', '0.2104', '0.05942', '-0.2273', '-0.0901', '0.2028', '0.6143', '-0.14', '0.05225', '-0.2146', '0.1726', '0.1323', '0.006927', '0.5356', '0.1395', '-0.01126', '0.3892', '0.429', '-0.221', '0.7905', '-0.0447', '0.512', '-0.3345', '0.38', '-0.005344']",C130988,,,759.89,,,
mondo:0013874,glucocorticoid deficiency 4,"['GCCD4', 'glucocorticoid deficiency 4 with or without mineralocorticoid deficiency', 'glucocorticoid deficiency type 4', 'NNT familial glucocorticoid deficiency', 'familial glucocorticoid deficiency caused by mutation in NNT', 'glucocorticoid deficiency 4', 'glucocorticoid deficiency 4, with or without mineralocorticoid deficiency']",,614736,,C3553587,,C131452,,,,,,
mondo:0013875,"3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome","['3-Methylglutaconic aciduria with dystonia-deafness, hepatopathy, encephalopathy, and Leigh-like syndrome', '3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome', '3-methylglutaconic aciduria with deafness-encephalopathy-Leigh-like syndrome', 'MGCA6', '3-MGCA type IV (formerly)', '3-MGCA-4 (formerly)', 'SERAC1 defect', '3-methylglutaconic aciduria caused by mutation in SERAC1', '3-methylglutaconic aciduria type VI', '3-methylglutaconic aciduria type 6', 'MEGDEL', '3-Methylglutaconic aciduria, type 6', 'SERAC1 3-methylglutaconic aciduria', 'MEGDEL syndrome']",0110001,614739,352328,C3553597,"['-0.191', '0.1506', '-0.1847', '-0.2427', '-0.28', '-0.4993', '0.1423', '0.1934', '-0.3743', '-0.07574', '-0.391', '-0.1715', '-0.183', '-0.1442', '0.01305', '0.05527', '0.083', '0.0113', '-0.4822', '-0.723', '0.2886', '-0.1807', '-0.1261', '-0.1414', '0.3743', '-0.01243', '-0.0676', '0.01104', '-0.5005', '-0.0875', '0.3079', '0.5903', '0.3523', '0.2856', '-0.0686', '-0.024', '-0.2285', '-0.03445', '-0.1913', '-0.1393', '-0.0001692', '0.0257', '0.2216', '0.2642', '-0.01886', '-0.7266', '0.1277', '-0.1709', '-0.01607', '0.1964', '-0.537', '-0.1454', '0.01244', '-0.2905', '0.1708', '-0.1542', '0.1279', '-0.03772', '-0.003595', '0.3777', '0.2057', '0.1609', '0.513', '-0.2211', '-0.378', '0.1464', '0.0947', '0.574', '-0.4805', '0.4353', '-0.6245', '0.1035', '-0.3716', '-0.1553', '-0.08826', '-0.4087', '0.2812', '0.2395', '-0.1036', '0.2747', '0.1675', '-0.1732', '-0.2402', '-0.1776', '0.1365', '0.169', '0.223', '0.1919', '0.23', '0.4514', '0.5044', '0.3386', '-0.1918', '0.0967', '0.5146', '0.7124', '0.1302', '-0.1186', '0.2966', '0.1831']",,,,,,,
mondo:0013876,"basal cell carcinoma, susceptibility to, 7","['susceptibility to basal cell carcinoma 7', 'skin basal cell carcinoma caused by mutation in TP53', 'basal cell carcinoma, susceptibility to, 7', 'basal cell carcinoma 7', 'BCC7', 'TP53 skin basal cell carcinoma', 'basal cell carcinoma, susceptibility to, type 7']",,614740,,,,,,,,,,
mondo:0013877,mitochondrial pyruvate carrier deficiency,"['MPYCD', 'mitochondrial pyruvate carrier deficiency']",0080363,614741,447784,C3553607,"['-0.0631', '0.05484', '-0.00819', '0.011284', '0.03528', '-0.05746', '-0.007286', '0.0671', '-0.01576', '-0.02461', '-0.01743', '0.000247', '0.01572', '-0.01657', '-0.002314', '-0.0329', '-0.01637', '-0.023', '-0.05875', '-0.10724', '-0.004948', '-0.04822', '0.0718', '-6.12e-05', '0.015434', '-0.02142', '-0.00256', '-0.01563', '-0.013504', '-0.03928', '0.05908', '0.004345', '0.06235', '0.02269', '-0.004276', '-0.0395', '-0.01527', '-0.02914', '-0.016', '-0.03772', '0.02258', '-0.08844', '0.01552', '-0.00942', '-0.02017', '-0.05075', '0.001357', '0.03', '0.01941', '0.03348', '-0.005524', '-0.0349', '0.00576', '-0.00331', '-0.0417', '-0.01611', '0.069', '-0.03278', '-0.0632', '0.03305', '0.0406', '0.02498', '0.0664', '0.0205', '0.005817', '0.02281', '0.06256', '0.05762', '-0.0695', '0.07153', '-0.03204', '0.002718', '-0.0199', '-0.01749', '0.04306', '0.05624', '0.02792', '-0.0215', '-0.02023', '-0.01133', '-0.009346', '-0.00282', '-0.01646', '0.0292', '0.03348', '0.01117', '0.01994', '0.03647', '0.08673', '0.01215', '0.0565', '0.05075', '0.0001792', '-0.00918', '0.1152', '0.063', '0.04388', '-0.09814', '-0.002934', '0.02509']",,,,,,,
mondo:0013878,"pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1","['pulmonary fibrosis and/or bone marrow failure, Telomere-related caused by mutation in TERT', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 1', 'PFBMFT1', 'pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 1', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related, 1', 'TERT pulmonary fibrosis and/or bone marrow failure, Telomere-related']",,614742,88,C3553617,"['0.4082', '-0.2185', '-0.69', '0.3286', '-0.1538', '-0.3594', '0.7896', '0.309', '-0.491', '-0.03992', '0.3247', '-0.2308', '-0.5864', '0.2788', '-0.3516', '-0.841', '-0.2634', '0.3015', '0.0558', '-0.439', '-0.1103', '-0.2537', '0.7207', '-1.07', '0.349', '-0.252', '0.465', '0.5547', '0.3635', '0.1445', '0.763', '-0.2957', '1.222', '-0.3113', '0.4346', '-0.1747', '-0.3516', '-0.2666', '0.4775', '0.388', '-0.4048', '-0.09015', '-0.3484', '0.1238', '0.02362', '-0.00747', '0.1652', '0.2761', '0.3035', '-0.2147', '-0.528', '-0.2006', '0.4854', '-0.1848', '-0.07306', '0.4917', '-0.4106', '0.663', '-0.587', '-0.3198', '-0.5444', '0.3481', '0.01904', '-0.2479', '-0.8545', '-0.33', '0.3286', '0.2037', '-0.588', '0.307', '-0.4617', '-0.2883', '0.6475', '-0.4385', '-0.07794', '0.4543', '0.254', '0.592', '0.2947', '-0.4182', '-0.6055', '-0.04532', '-0.0907', '-0.0834', '7.58e-05', '0.4912', '0.219', '0.656', '0.1885', '0.2505', '0.3533', '-0.6543', '-0.702', '0.3733', '0.6973', '0.2668', '-0.1698', '-0.1181', '-0.6216', '-0.3438']",,1001501,,,,,
mondo:0013879,"pulmonary fibrosis and/or bone marrow failure, Telomere-related, 2","['pulmonary fibrosis, idiopathic, susceptibility to', 'pulmonary fibrosis and/or bone marrow failure, TELOMERE-RELATED, 2', 'aplastic anemia', 'PFBMFT2', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related, type 2', 'aplastic anaemia', 'pulmonary fibrosis and/or bone marrow failure, Telomere-related, 2']",,614743,88,C3553622,,,,,,,,
mondo:0013880,"facial paresis, hereditary congenital, 3","['HOXB1 congenital hereditary facial paralysis-variable hearing loss syndrome', 'HCFP3', 'facial paresis, hereditary congenital, 3', 'facial paresis, hereditary congenital, type 3', 'congenital hereditary facial paralysis-variable hearing loss syndrome caused by mutation in HOXB1']",,614744,,C3553625,,,,,,,,
mondo:0013881,"pidermolysis bullosa, junctional 7, with interstitial lung disease and nephrotic syndrome","['ILNEB', 'congenital NEP syndrome', 'JEB with respiratory and renal involvement', 'JEB-RR', 'congenital interstitial lung disease-nephrotic syndrome-epidermolysis bullosa syndrome', 'congenital nephrotic syndrome-epidermolysis bullosa-pulmonary disease syndrome', 'junctional epidermolysis bullosa with respiratory and renal involvement', 'interstitial lung disease, nephrotic syndrome, and epidermolysis bullosa, congenital', 'congenital nephrotic syndrome - interstitial lung disease - epidermolysis bullosa syndrome', 'congenital ILNEB syndrome']",,614748,306504,C3553636,"['0.7915', '-0.2056', '-0.4321', '0.258', '-0.0629', '-0.957', '-0.521', '0.3696', '0.00116', '-0.612', '0.4644', '-0.2308', '-0.8887', '0.5635', '-0.647', '-0.3298', '0.0397', '-0.8794', '-0.1937', '-0.732', '-0.11194', '-0.0383', '0.5156', '0.5', '0.3052', '0.1758', '-0.8364', '0.9976', '0.01266', '-0.817', '0.454', '-0.1148', '-0.2399', '-0.07806', '-0.138', '-0.12', '-1.301', '0.3188', '0.955', '-0.383', '0.04147', '-0.509', '0.1611', '0.11884', '-0.10443', '0.02412', '-0.3167', '0.1814', '0.531', '-0.2097', '-0.6167', '-0.2228', '0.4517', '0.07855', '-0.095', '-0.667', '-0.0733', '0.9644', '-0.586', '-0.28', '0.207', '0.308', '-0.1407', '0.4104', '0.943', '0.706', '0.264', '0.3765', '-0.8228', '-0.0842', '-0.1361', '-0.01213', '-0.4058', '-0.03696', '-0.12366', '-0.1906', '0.1111', '0.144', '-0.0952', '-0.11786', '-0.948', '0.2268', '-0.04346', '-0.08', '0.2048', '0.2478', '-0.7744', '0.6284', '0.8076', '0.526', '-0.277', '0.3923', '-0.01475', '0.3745', '-0.05652', '0.7324', '0.1403', '-0.64', '0.8296', '0.268']",,,,,,,
mondo:0013882,hyperphosphatasia with intellectual disability syndrome 2,"['PIGO hyperphosphatasia-intellectual disability syndrome', 'hyperphosphatasia with intellectual disability syndrome type 2', 'hyperphosphatasia with mental retardation syndrome 2', 'hyperphosphatasia with mental retardation syndrome type 2', 'HPMRS2', 'hyperphosphatasia with intellectual disability syndrome 2', 'hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGO', 'glycosylphosphatidylinositol biosynthesis defect 6']",,614749,,C3553637,,,,,,,,
mondo:0013883,congenital myasthenic syndrome 13,"['myasthenic syndrome, congenital, with tubular aggregates 2', 'myasthenic syndrome, congenital, 13', 'congenital myasthenic syndrome with tubular aggregates 2', 'myasthenic syndrome, congenital, 13, with tubular aggregates', 'CMS13', 'congenital myasthenic syndrome 13 with tubular aggregates', 'congenital myasthenic syndromes with glycosylation defect caused by mutation in DPAGT1', 'myasthenic syndrome, congenital, type 13', 'DPAGT1 congenital myasthenic syndromes with glycosylation defect', 'CMSTA2', 'congenital myasthenic syndrome type 13']",0110676,614750,,C3553645,,,,,,,,
mondo:0013884,"neuronopathy, distal hereditary motor, type 5B","['neuronopathy, distal hereditary motor caused by mutation in REEP1', 'REEP1 neuronopathy, distal hereditary motor', 'neuronopathy, distal hereditary motor, type VB', 'dHMN 5B', 'spinal muscular atrophy, distal, type 5B', 'HMN5B', 'HMN 5B', 'neuropathy, distal hereditary motor, type 5B']",0111205,614751,,C3553656,,,,,,,,
mondo:0013885,Malan overgrowth syndrome,"['SOTOS2', 'Sotos syndrome 2', 'Malan syndrome', 'Sotos syndrome type 2']",0112102,614753,420179,C3553660,,,,,,,,
mondo:0013886,cerebellar dysfunction with variable cognitive and behavioral abnormalities,"['cerebellar ataxia, nonprogressive, with mental retardation', 'non-progressive cerebellar ataxia with intellectual disability', 'cerebellar ataxia, nonprogressive, with intellectual disability', 'cerebellar dysfunction with variable cognitive and behavioral abnormalities', 'nonprogressive cerebellar ataxia with mental retardation', 'CANPMR', 'nonprogressive cerebellar ataxia with intellectual disability']",0050998,614756,314647,C3553661,"['0.1884', '0.2096', '-0.3958', '-0.5903', '-0.2119', '-0.7275', '-0.1421', '0.5537', '-0.9097', '-0.6274', '-0.2145', '0.0786', '0.02977', '-0.10394', '0.1979', '-0.2107', '0.3892', '-0.869', '0.4573', '-0.546', '-0.0629', '0.0232', '0.1534', '0.1472', '0.4412', '0.2012', '-0.0711', '-0.0354', '0.3042', '-0.2676', '0.2438', '0.46', '0.3254', '0.2612', '0.05304', '0.07166', '-0.791', '-0.3318', '-0.502', '-0.1266', '0.7427', '-0.478', '-0.2998', '0.6016', '-0.06824', '-0.251', '0.0691', '0.939', '0.3032', '-0.606', '-0.2515', '0.1088', '-0.6562', '-0.2466', '-0.3477', '-0.3022', '0.333', '-0.05753', '0.06223', '0.5635', '-0.0985', '0.2861', '-0.054', '0.2324', '-0.2246', '-0.1997', '-0.0111', '0.07666', '-0.2206', '0.7925', '-0.03934', '0.248', '0.341', '-0.3044', '-0.03156', '0.7163', '0.5376', '-0.1769', '-0.04953', '0.3997', '0.1538', '-0.4192', '-0.3906', '0.226', '0.0964', '0.1653', '-0.2153', '0.6', '0.529', '0.6655', '0.11835', '0.623', '0.6226', '-0.00549', '0.8447', '0.3547', '0.523', '-0.1124', '0.3167', '0.271']",,,,,,,
mondo:0013887,"heterotaxy, visceral, 6, autosomal","['HTX6', 'heterotaxy, visceral, 6, autosomal recessive', 'heterotaxy, visceral, 6, autosomal']",,614779,,C3553676,,,,,,,,
mondo:0013888,"tremor, hereditary essential, 4","['essential tremor, hereditary, 4', 'FUS essential tremor', 'tremor, hereditary essential, type 4', 'tremor, hereditary essential, 4', 'ETM4', 'essential tremor caused by mutation in FUS']",0111431,614782,,C3539195,,,,,,,,
mondo:0013889,short stature-optic atrophy-Pelger-HuC+t anomaly syndrome,"['soph syndrome', 'short stature, optic nerve atrophy, and Pelger-Huet anomaly', 'soph', 'short stature with optic atrophy and Pelger-Huët anomaly syndrome', 'short stature-optic atrophy-Pelger-Huët anomaly syndrome']",,614800,391677,C3541319,"['-0.717', '-0.11993', '0.392', '-0.2367', '0.2208', '0.03473', '-0.2175', '0.8145', '-0.394', '-0.001402', '-0.1598', '-0.06006', '0.11005', '-0.1598', '-0.38', '-0.0288', '0.475', '-0.05038', '-0.2715', '-0.4985', '0.0913', '-0.10803', '-0.005238', '-0.145', '-0.07556', '-0.0761', '-0.1841', '0.01762', '0.06116', '0.02351', '0.2522', '-0.1066', '0.3608', '0.0825', '0.01865', '0.1576', '0.0679', '-0.044', '-0.03036', '-0.1907', '0.1475', '-0.208', '-0.2146', '-0.1746', '-0.1945', '-0.1261', '-0.1572', '0.3225', '0.1276', '0.11755', '-0.003004', '0.1053', '0.11224', '0.381', '-0.154', '-0.3154', '-0.2559', '-0.2056', '-0.075', '-0.01527', '0.09796', '0.01226', '-0.4817', '-0.11633', '-0.0683', '-0.2231', '0.3337', '0.594', '-0.2354', '0.559', '-0.2976', '0.4133', '0.2537', '-0.04074', '-0.09406', '-0.1813', '0.0686', '-0.2842', '-0.10187', '-0.0575', '0.01878', '-0.04825', '0.1384', '0.5894', '-0.08954', '-0.2137', '-0.09015', '0.199', '0.4697', '0.3691', '0.02084', '0.2415', '0.2119', '0.2856', '0.4497', '-0.0845', '0.4731', '-0.3833', '0.2585', '0.3118']",,,,,,,
mondo:0013890,congenital myopathy with internal nuclei and atypical cores,"['CNM4', 'centronuclear myopathy 4', 'centronuclear myopathy type 4', 'myopathy, centronuclear, 4', 'myopathy, centronuclear, type 4']",0111224,614807,319160,C3553709,"['-0.4692', '0.04205', '-0.06995', '-0.01917', '0.01487', '-0.3481', '0.4573', '1.084', '-0.8574', '0.2512', '-0.2361', '-0.0652', '-0.2051', '-0.1111', '-0.01999', '0.05853', '0.04102', '0.0622', '-0.585', '-0.9663', '0.519', '0.36', '0.1959', '0.3347', '0.004524', '-0.1683', '-0.06433', '-0.64', '-0.2659', '0.1406', '0.523', '0.1086', '0.2133', '0.2339', '0.2311', '-0.1251', '-0.2688', '-0.4019', '0.1036', '-0.1621', '-0.0851', '-0.298', '-0.3682', '0.589', '-0.1443', '0.1321', '-0.415', '0.0823', '-0.2483', '0.583', '-0.2734', '0.209', '-0.08716', '-0.0652', '-0.603', '-0.2446', '0.4177', '-0.2413', '0.4172', '-0.1713', '0.2615', '0.2279', '0.1272', '0.1642', '-0.5347', '0.06113', '0.1748', '0.633', '-0.1174', '0.3333', '-0.08374', '0.2124', '0.1383', '0.1796', '0.2096', '0.03445', '-0.1231', '-0.07166', '-0.4834', '-0.2452', '0.1544', '-0.1462', '0.1085', '0.2954', '-0.1287', '0.1853', '-0.1525', '0.1406', '0.476', '-0.1284', '0.7393', '0.129', '0.2041', '0.04648', '0.509', '0.2563', '0.707', '-0.1516', '-0.0597', '-0.1603']",,,,,,,
mondo:0013891,amyotrophic lateral sclerosis type 18,"['ALS18', 'amyotrophic lateral sclerosis type 18', 'PFN1 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis caused by mutation in PFN1', 'amyotrophic lateral sclerosis 18']",0060209,614808,,C3553719,,,,,,,,
mondo:0013892,C3 glomerulonephritis,"['complement-mediated membranoproliferative glomerulonephritis', 'nephropathy due to CFHR5 deficiency', 'CFHR5 deficiency']",,614809,329931,CN187045,"['0.831', '0.3857', '-0.628', '0.2362', '-0.1289', '-0.2505', '0.01851', '0.167', '-0.4958', '-0.1588', '0.06647', '-0.2615', '-0.4004', '1.007', '-0.2742', '-0.2484', '-0.1073', '0.4478', '0.832', '-0.01181', '-0.11487', '-1.125', '0.7485', '-0.07275', '0.643', '-0.2013', '-0.8013', '0.8613', '0.10315', '-0.3064', '0.1875', '0.2673', '0.719', '-0.034', '-0.1178', '-0.1163', '-0.4958', '0.5044', '0.505', '-0.5776', '-0.5186', '-0.3074', '-0.3096', '-0.46', '0.2313', '-0.4304', '-0.5205', '-0.406', '-0.1005', '-0.01936', '0.3286', '0.1467', '1.127', '-0.412', '-0.6226', '-0.1517', '-0.0653', '0.02003', '-0.653', '-0.6743', '-0.6846', '0.11566', '-0.02492', '-0.1119', '-0.3413', '-0.4492', '0.1434', '0.467', '-0.7695', '0.6484', '-0.8594', '0.27', '0.5205', '-0.2144', '-0.12213', '0.1826', '0.617', '0.9907', '-0.1733', '0.2996', '-0.4143', '0.1866', '0.05334', '0.2876', '0.1498', '-0.21', '0.1425', '-0.3413', '0.1399', '0.9863', '0.799', '0.4048', '-0.625', '0.1346', '0.553', '0.7666', '-0.2886', '-0.694', '-0.8647', '0.0659']",C123043,,,,,,
mondo:0013893,"multiple sclerosis, susceptibility to, 5","['multiple sclerosis, susceptibility to, 5', 'susceptibility to multiple sclerosis 5', 'TNFRSF1A multiple sclerosis, susceptibility to', 'MS5', 'multiple sclerosis, susceptibility to caused by mutation in TNFRSF1A', 'multiple sclerosis, susceptibility to, type 5']",,614810,,,,,,,,,,
mondo:0013894,short stature-onychodysplasia-facial dysmorphism-hypotrichosis syndrome,"['short stature, onychodysplasia, facial dysmorphism, and hypotrichosis', 'soft syndrome', 'soft']",,614813,314394,C3542022,"['-0.3647', '0.008705', '0.5083', '-0.3684', '0.4272', '-0.4468', '-0.3928', '0.4177', '-0.639', '-0.2148', '0.2079', '0.03894', '0.1027', '-0.08124', '-0.1372', '0.2546', '0.797', '-0.09454', '-0.279', '-0.854', '-0.06525', '-0.0684', '0.3645', '-0.1407', '0.288', '0.01093', '-0.1752', '0.04343', '0.581', '-0.1945', '0.293', '-0.3093', '0.1833', '0.0926', '0.504', '-0.0816', '-0.2766', '-0.3079', '0.1316', '-0.839', '0.09644', '-0.3386', '-0.0643', '-0.1443', '0.1746', '-0.62', '-0.0803', '0.7637', '0.2037', '-0.0503', '-0.3203', '-0.02605', '0.0347', '0.5776', '-0.473', '-0.482', '-0.493', '-0.1498', '0.1616', '0.0895', '0.06256', '0.418', '-0.329', '-0.1732', '0.134', '0.2683', '0.17', '0.3877', '0.01041', '0.4673', '-0.778', '0.0065', '0.0923', '-0.1304', '-0.2612', '-0.2292', '0.2184', '-0.10565', '-0.2588', '0.2021', '0.1098', '0.3628', '0.03577', '0.192', '-0.1033', '-0.1823', '-0.2913', '0.4473', '0.5415', '0.4773', '-0.2352', '0.2319', '0.2222', '0.0966', '0.5015', '-0.02925', '0.3154', '-0.5244', '0.4895', '0.06256']",,,,,,,
mondo:0013895,Adams-Oliver syndrome 3,"['RBPJ Adams-Oliver syndrome', 'Adams-Oliver syndrome 3', 'Adams-Oliver syndrome caused by mutation in RBPJ', 'AOS3', 'Adams-Oliver syndrome type 3']",,614814,,C3553748,,,,,,,,
mondo:0013896,Joubert syndrome 18,"['Joubert syndrome type 18', 'JBTS18', 'TCTN3 Joubert syndrome', 'Joubert syndrome caused by mutation in TCTN3', 'Joubert syndrome 18']",0110987,614815,,C3553758,,,,,,,,
mondo:0013897,Loeys-Dietz syndrome 4,"['aneurysm, aortic and cerebral, with arterial tortuosity and skeletal manifestations', 'Loeys-Dietz syndrome type 4', 'TGFB2 Loeys-Dietz syndrome', 'Loeys-Dietz syndrome caused by mutation in TGFB2', 'LDS4', 'Loeys-Dietz syndrome 4']",0070233,614816,,C3553762,,,,,,,,
mondo:0013898,karyomegalic interstitial nephritis,"['systemic karyomegaly', 'kin', 'interstitial nephritis, karyomegalic', 'KMIN', 'FAN1 interstitial nephritis', 'interstitial nephritis caused by mutation in FAN1']",0060911,614817,401996,C3553774,"['-0.2693', '-0.0583', '0.11096', '-0.2542', '-0.1505', '-0.333', '0.02899', '0.43', '-0.5303', '-0.1163', '0.07513', '0.1849', '-0.4585', '0.01587', '0.2426', '-0.596', '-0.12256', '-0.05762', '0.3015', '-0.5815', '0.3547', '-0.1998', '0.2817', '0.1274', '0.4412', '-0.2559', '0.2295', '0.6', '-0.0105', '0.143', '0.3147', '-0.07806', '0.2559', '-0.1554', '0.4314', '-0.4072', '-0.842', '0.0621', '0.1656', '-0.1743', '-0.1553', '-0.233', '0.3452', '0.3591', '-0.328', '-0.4922', '-0.4038', '-0.3406', '0.2162', '-0.1598', '0.05475', '0.4277', '0.1093', '-0.4858', '-0.043', '-0.7065', '0.2795', '0.1259', '-0.8354', '-0.06198', '0.2979', '0.3298', '-0.11536', '-0.135', '0.4092', '-0.3176', '0.5747', '0.3755', '-0.1843', '0.2634', '-0.352', '-0.295', '0.2059', '0.2307', '-0.085', '-0.4937', '0.45', '0.4316', '0.02422', '0.0598', '-0.286', '0.1466', '0.573', '0.0801', '-0.4802', '-0.1055', '0.2333', '0.267', '0.1063', '-0.098', '0.575', '0.222', '-0.1914', '-0.1245', '0.8076', '0.605', '0.51', '-0.3252', '-0.12054', '0.274']",C173626,,,,,,
mondo:0013899,Weill-Marchesani syndrome 3,"['WMS3', 'Weill-Marchesani syndrome type 3', 'Weill-Marchesani syndrome 3, recessive', 'Weill-Marchesani syndrome caused by mutation in LTBP2', 'Weill-Marchesani syndrome 3', 'LTBP2 Weill-Marchesani syndrome']",,614819,,C3553785,,,,,,,,
mondo:0013900,alternating hemiplegia of childhood 2,"['AHC2', 'ATP1A3 alternating hemiplegia of childhood', 'alternating hemiplegia of childhood 2', 'alternating hemiplegia of childhood caused by mutation in ATP1A3', 'alternating hemiplegia of childhood type 2']",,614820,,C3553788,,,,,,,,
mondo:0013901,spermatogenic failure 10,"['azoospermia caused by mutation in SEPT12', 'SPGF10', 'spermatogenic failure type 10', 'spermatogenic failure with defective sperm annulus', 'spermatogenic failure 10', 'SEPT12 azoospermia']",0070178,614822,,C3553793,,,,,,,,
mondo:0013902,aortic valve disease 2,"['bicuspid aortic valve', 'AOVD2', 'aortic valve disease type 2', 'aortic valve disease 2', 'aortic valve disease caused by mutation in SMAD6', 'SMAD6 aortic valve disease', 'aortic valve stenosis']",0080334,614823,,C3542024,,,,,,,,
mondo:0013903,"nystagmus 7, congenital, autosomal dominant","['NYSTAGMUS 7, congenital, autosomal dominant', 'NYS7']",0111791,614826,,C3553801,,,,,,,,
mondo:0013904,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8","['muscular dystrophy-dystroglycanopathy, type A caused by mutation in POMGNT2', 'Walker-Warburg syndrome or muscle-eye-brain disease, Gtdc2-related', 'POMGNT2 muscular dystrophy-dystroglycanopathy, type A', 'MDDGA8', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 8', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 8', 'muscle-eye-brain-POMGNT2 related', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 8']",0111231,614830,899,C3553813,,,,,,,,
mondo:0013905,autosomal recessive spinocerebellar ataxia 13,"['SCAR13', 'GRM1 autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome', 'autosomal recessive congenital cerebellar ataxia due to metabotropic glutamate receptor 1 deficiency', 'autosomal recessive spinocerebellar ataxia type 13', 'autosomal recessive cerebellar ataxia-pyramidal signs-nystagmus-oculomotor apraxia syndrome caused by mutation in GRM1', 'GRM1 autosomal recessive cerebellar ataxia - pyramidal signs - nystagmus - oculomotor apraxia syndrome', 'spinocerebellar ataxia, autosomal recessive type 13', 'autosomal recessive congenital cerebellar ataxia due to MGLUR1 deficiency', 'spinocerebellar ataxia, autosomal recessive 13']",0080062,614831,324262,C3553816,"['-0.11646', '-0.344', '0.11255', '-0.1273', '-0.3542', '-0.88', '0.1705', '-0.11755', '-0.6567', '-0.8', '0.11005', '0.3315', '-0.173', '0.07513', '0.4338', '-0.3125', '-0.2317', '-0.3853', '0.05292', '-0.838', '-0.1865', '-0.285', '0.1853', '-0.3735', '0.602', '-0.377', '-0.1687', '0.3206', '-0.16', '-0.808', '-0.04562', '0.4517', '-0.4683', '-0.10834', '0.3923', '-0.03653', '-0.333', '0.0683', '0.563', '0.277', '0.275', '0.2896', '-0.4673', '0.5034', '0.3806', '-0.4624', '0.168', '0.5776', '0.3567', '-0.1127', '-0.1837', '0.2313', '-0.03436', '-0.5044', '-0.02187', '-0.758', '0.1959', '0.5444', '-0.2238', '0.631', '-0.6895', '0.257', '0.338', '-0.1428', '-0.4282', '0.516', '0.1509', '0.5073', '-0.568', '0.4763', '1.023', '0.5776', '-0.03244', '-0.6006', '0.585', '0.4116', '0.4934', '0.2637', '0.1952', '0.5215', '-0.3936', '-0.7974', '0.252', '0.886', '-0.2057', '-0.5596', '0.1744', '0.0591', '0.51', '0.6846', '0.543', '0.669', '-0.01576', '0.08997', '1.048', '1.082', '0.4429', '0.3271', '-0.3252', '0.0079']",,,,,,,
mondo:0013906,amelogenesis imperfecta hypomaturation type 2A4,"['amelogenesis imperfecta caused by mutation in ODAPH', 'AI2A4', 'ODAPH amelogenesis imperfecta', 'amelogenesis imperfecta hypomaturation type IIA4', 'amelogenesis imperfecta, type IIA4', 'amelogenesis imperfecta type IIA4', 'amelogenesis imperfecta, hypomaturation type, IIA4']",0110062,614832,,C3553830,,,,,,,,
mondo:0013907,bilateral generalized polymicrogyria,"['bilateral generalized polymicrogyria', 'microcephaly, short stature, and polymicrogyria with seizures', 'polymicrogyria with seizures', 'microcephaly, short stature, and polymicrogyria with or without seizures', 'PMGYS', 'MSSP']",0080920,,208447,C3553831,"['0.10175', '0.4116', '0.2457', '-0.0557', '0.077', '-0.2457', '0.2377', '-0.0542', '-0.4478', '-0.0615', '-0.409', '-0.1682', '-0.2085', '0.1311', '0.2676', '0.02782', '-0.00543', '-0.342', '-0.403', '-0.548', '-0.2217', '0.11926', '0.289', '-0.1935', '0.02995', '-0.283', '-0.1866', '0.2351', '0.007507', '0.2072', '0.1986', '0.1179', '0.3325', '-0.1586', '0.01663', '0.2051', '-0.1428', '0.03275', '0.2242', '0.05527', '0.3955', '-0.0932', '-0.1514', '0.11633', '0.3108', '-0.04385', '0.0181', '0.02083', '-0.005375', '-0.0953', '0.386', '-0.09454', '0.1688', '-0.2428', '-0.1864', '0.3787', '0.1055', '0.2028', '-0.11096', '0.0526', '-0.00834', '-0.004776', '0.529', '0.1542', '-0.2325', '0.3306', '0.2612', '0.0994', '-0.3108', '0.3953', '-0.204', '0.0673', '0.3013', '-0.01585', '-0.0895', '0.4763', '0.2754', '0.2505', '-0.02121', '-0.2893', '-0.291', '-0.2028', '-0.1494', '0.319', '-0.04926', '-0.1765', '-0.0001065', '0.1279', '0.204', '0.4587', '-0.1155', '0.438', '-0.0163', '0.3376', '0.32', '0.2454', '0.2427', '-0.3254', '0.3296', '0.07245']",,,,,,,
mondo:0013908,"thyrotoxic periodic paralysis, susceptibility to, 3","['TTPP3', 'thyrotoxic periodic paralysis, susceptibility to, 3']",,614834,,,,,,,,,,
mondo:0013909,"human herpesvirus 8, susceptibility to","['HHV8S', 'HHV-8, susceptibility to', 'HUMAN HERPESVIRUS 8, susceptibility to']",,614836,,,,,,,,,,
mondo:0013910,hypogonadotropic hypogonadism 8 with or without anosmia,"['hypogonadotropic hypogonadism 8 with or without anosmia', 'KISS1R hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism caused by mutation in KISS1R', 'HH8']",0090074,614837,,C3553841,,,,,,E23.0,,
mondo:0013911,hypogonadotropic hypogonadism 9 with or without anosmia,"['hypogonadotropic hypogonadism caused by mutation in NSMF', 'hypogonadotropic hypogonadism 9 with or without anosmia', 'NSMF hypogonadotropic hypogonadism', 'HH9']",0090085,614838,,C3553842,,,,,,E23.0,,
mondo:0013912,hypogonadotropic hypogonadism 10 with or without anosmia,"['hypogonadotropic hypogonadism 10 with or without anosmia', 'HH10', 'hypogonadotropic hypogonadism caused by mutation in TAC3', 'TAC3 hypogonadotropic hypogonadism']",0090089,614839,,C3553843,,,,,,E23.0,,
mondo:0013913,hypogonadotropic hypogonadism 11 with or without anosmia,"['hypogonadotropic hypogonadism caused by mutation in TACR3', 'HH11', 'hypogonadotropic hypogonadism 11 with or without anosmia', 'TACR3 hypogonadotropic hypogonadism']",0090071,614840,,C3553844,,,,,,E23.0,,
mondo:0013914,hypogonadotropic hypogonadism 12 with or without anosmia,"['eunuchoidism familial hypogonadotropic', 'familial idiopathic gonadotrpin deficiency', 'eunuchoidism, familial hypogonadotropic', 'FIGD', 'gonadotropin deficiency familial idiopathic', 'familial hypogonadotrophic eunuchoidism', 'familial hypogonadotropic eunuchoidism', 'hypogonadotropic hypogonadism 12 with or without anosmia', 'HH12', 'gonadotropin deficiency, familial idiopathic']",0090072,614841,,C1856897,,,,C535764,,E23.0,,
mondo:0013915,hypogonadotropic hypogonadism 13 with or without anosmia,"['hypogonadotropic hypogonadism 13 with or without anosmia', 'HH13', 'KISS1 hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism caused by mutation in KISS1']",0090073,614842,,C3541462,,,,,,E23.0,,
mondo:0013916,nephronophthisis 14,"['nephronophthisis 14', 'ZNF423 nephronophthisis (disease)', 'NPHP14', 'nephronophthisis type 14', 'Joubert syndrome 19']",0111122,614844,2318,C3539071,,,,,,,,
mondo:0013917,nephronophthisis 15,"['CEP164 nephronophthisis (disease)', 'NPHP15', 'nephronophthisis type 15', 'nephronophthisis 15']",0111123,614845,,C3541853,,,,,,,,
mondo:0013918,distal tetrasomy 15q,"['tetrasomy 15(q25-qter)', 'levy-Shanske syndrome', 'tetrasomy 15q26', 'distal tetrasomy type 15q', 'tetrasomy type 15Q26']",,614846,314588,CN203770,,,,,,,,
mondo:0013919,"epilepsy, idiopathic generalized, susceptibility to, 12","['EIG12', 'epilepsy, idiopathic generalized, susceptibility to, type 12', 'epilepsy, idiopathic generalized, susceptibility to, 12', 'susceptibility to idiopathic generalized epilepsy 12', 'susceptibility to idiopathic generalised epilepsy 12']",0111313,614847,,,,,,,,,,
mondo:0013920,"herpes simplex encephalitis, susceptibility to, 3","['herpes simplex encephalitis caused by mutation in TRAF3', 'herpes simplex encephalitis, susceptibility to, 3', 'Herpes simplex encephalitis, susceptibility to, type 3', 'IIAE5', 'encephalopathy, acute, infection-induced, susceptibility to, 5', 'TRAF3 herpes simplex encephalitis', 'encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 5', 'encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 5']",,614849,,,,,,,,,,
mondo:0013921,"herpes simplex encephalitis, susceptibility to, 4","['herpes simplex encephalitis, susceptibility to, 4', 'encephalopathy, acute, infection-induced, susceptibility to, 6', 'encephalopathy, acute, infection-induced (HERPES-specific), susceptibility to, 6', 'encephalopathy, acute, infection-induced (Herpes-specific), susceptibility to, 6', 'Herpes simplex encephalitis, susceptibility to, type 4', 'herpes simplex encephalitis caused by mutation in TICAM1', 'TICAM1 herpes simplex encephalitis', 'IIAE6']",,614850,,,,,,,,,,
mondo:0013922,Seckel syndrome 7,"['Seckel syndrome type 7', 'Seckel syndrome 7', 'microcephalic primordial dwarfism, Dauber type', 'Seckel syndrome caused by mutation in NIN', 'NIN Seckel syndrome', 'SCKL7']",0070011,614851,319675,C3553870,"['-0.3838', '0.1692', '0.644', '-0.4167', '0.2108', '-0.2786', '0.1576', '0.7104', '-0.5103', '-0.194', '-0.2725', '-0.002075', '0.1343', '0.0733', '-0.2323', '0.04205', '0.5146', '-0.08075', '-0.305', '-0.7695', '-0.04776', '0.10156', '0.3696', '-0.06055', '0.037', '-0.00637', '-0.1345', '-0.1132', '0.401', '-0.2695', '0.144', '-0.1758', '0.5684', '0.35', '0.1478', '-0.06586', '-0.1163', '-0.372', '-0.3206', '-0.1909', '0.06793', '-0.1472', '-0.2126', '-0.0673', '-0.1881', '-0.2373', '0.06116', '0.412', '-0.02866', '0.188', '-0.0705', '-0.1155', '-0.2732', '0.1279', '-0.3567', '-0.306', '-0.3008', '-0.304', '0.0302', '0.3884', '0.1054', '-0.0961', '-0.3503', '0.151', '-0.10913', '-0.06287', '0.103', '0.2097', '-0.283', '0.1768', '-0.3647', '0.2184', '0.306', '-0.2449', '-0.248', '-0.0089', '0.0679', '-0.1438', '-0.3933', '-0.0601', '-0.129', '0.1725', '-0.3057', '0.3481', '0.04855', '-0.019', '-0.06604', '0.4028', '0.5137', '0.3103', '0.00911', '0.4275', '0.10455', '0.06198', '0.2961', '0.104', '0.527', '-0.3245', '0.6353', '0.1747']",,,,,,,
mondo:0013923,"microcephaly 9, primary, autosomal recessive","['MCPH9', 'CEP152 autosomal recessive primary microcephaly', 'microcephaly 9, primary, autosomal recessive', 'autosomal recessive primary microcephaly caused by mutation in CEP152']",0070292,614852,,C3553886,,,,,,,,
mondo:0013924,osteogenesis imperfecta type 13,"['BMP1 osteogenesis imperfecta', 'osteogenesis imperfecta caused by mutation in BMP1', 'osteogenesis imperfecta type XIII', 'OI, type 13', 'osteogenesis imperfecta, type XIII', 'osteogenesis imperfecta, type 13', 'OI13']",0110342,614856,216812,C3553887,,,,,,,,
mondo:0013925,"methylmalonic acidemia with homocystinuria, type cblJ","['methylmalonic acidemia with homocystinuria type cblJ', 'methylmalonic aciduria with homocystinuria, type cblJ', 'methylmalonic aciduria and homocystinuria, cblJ type', 'MAHCJ', 'cobalamin J defect', 'cblJ defects', 'combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblJ']",,614857,369955,C3553915,"['-0.03348', '0.1359', '0.02513', '-0.00791', '0.0279', '-0.2102', '-0.0671', '0.1509', '-0.0783', '-0.011246', '-0.1764', '-0.1023', '0.0678', '-0.0628', '0.002296', '-0.0877', '-0.010666', '-0.09106', '-0.1154', '-0.2411', '-0.0953', '-0.1159', '0.07654', '-0.07715', '0.12067', '0.02138', '-0.03488', '-0.0997', '0.0743', '-0.11633', '0.00824', '0.1268', '0.1505', '0.1143', '0.0845', '-0.08307', '0.01294', '-0.2573', '-0.06064', '-0.1359', '0.04282', '-0.2473', '0.0387', '-0.0519', '-0.1641', '-0.164', '-0.005013', '0.1171', '-0.05792', '0.0574', '-0.07556', '-0.1167', '-0.0117', '-0.001493', '-0.1257', '-0.03342', '0.1866', '-0.0574', '-0.1932', '0.1604', '0.1781', '0.0579', '0.076', '-0.0414', '-0.00559', '-0.003824', '0.2118', '0.01715', '-0.1594', '0.1619', '-0.0935', '-0.003128', '-0.1054', '-0.2256', '0.06143', '0.0793', '0.01384', '-0.1556', '-0.09265', '0.05118', '0.136', '0.02263', '-0.1158', '0.1376', '0.04092', '0.08984', '-0.014336', '0.236', '0.2279', '0.04126', '0.1259', '0.0924', '0.02719', '-0.00498', '0.316', '0.2009', '0.1755', '-0.2123', '-0.011925', '0.06235']",,,,,,,
mondo:0013926,hypogonadotropic hypogonadism 14 with or without anosmia,"['WDR11 hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism caused by mutation in WDR11', 'hypogonadotropic hypogonadism 14 with or without anosmia', 'HH14']",0090087,614858,,C3540450,,,,,,E23.0,,
mondo:0013927,peroxisome biogenesis disorder 3A (Zellweger),"['PBD3A', 'peroxisome biogenesis disorder, complementation group 3', 'peroxisome biogenesis disorder 3A (Zellweger)']",0080478,614859,,C3553929,,C155752,,C566633,,,,
mondo:0013928,dystonia 23,"['dystonia 23', 'DYT23', 'dystonia type 23', 'dystonic disorder caused by mutation in CACNA1B', 'CACNA1B dystonic disorder', 'adult-onset cervical dystonia, DYT23 type']",0090051,614860,420492,C3538999,,,,,,,,
mondo:0013929,autosomal recessive nonsyndromic hearing loss 98,"['autosomal recessive deafness 98', 'DFNB98', 'autosomal recessive nonsyndromic deafness caused by mutation in TSPEAR', 'autosomal recessive nonsyndromic deafness 98', 'deafness, autosomal recessive type 98', 'TSPEAR autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 98', 'deafness, autosomal recessive 98']",0110540,614861,,C3553932,,,,,,,,
mondo:0013930,peroxisome biogenesis disorder 4A (Zellweger),"['PBD4A', 'peroxisome biogenesis disorder, complementation group C', 'peroxisome biogenesis disorder 4A (Zellweger)', 'peroxisome biogenesis disorder, complementation group 6', 'peroxisome biogenesis disorder, complementation group 4', 'classic peroxisome biogenesis disorder']",0080479,614862,,C3553936,,C155754,,C563301,,,,
mondo:0013931,peroxisome biogenesis disorder 4B,"['peroxisome biogenesis disorder 4B', 'PBD4B', 'peroxisome biogenesis disorder type 4B', 'non-classic peroxisome biogenesis disorder']",,614863,,C3553937,,C155755,,,,,,
mondo:0013932,peroxisome biogenesis disorder 5A (Zellweger),"['peroxisome biogenesis disorder, complementation group 5', 'peroxisome biogenesis disorder, complementation group 10', 'peroxisome biogenesis disorder, complementation group F', 'peroxisome biogenesis disorder 5A (Zellweger)', 'PBD5A']",0080480,614866,,C3553940,,C155756,,,,,,
mondo:0013933,peroxisome biogenesis disorder 5B,"['PBD5B', 'peroxisome biogenesis disorder type 5B', 'peroxisome biogenesis disorder 5B']",,614867,,C3542026,,C155757,,,,,,
mondo:0013934,combined immunodeficiency due to STK4 deficiency,"['T-cell immunodeficiency, recurrent infections, and autoimmunity with or without CARDIAC malformations', 'T-cell immunodeficiency, recurrent infections, autoimmunity, and cardiac malformations', 'TIIAC', 'MST1 deficiency', 'STK4 deficiency', 'CID due to STK4 deficiency']",,614868,314689,C3553943,"['-0.2979', '0.3416', '0.4338', '-0.833', '0.398', '-0.2333', '0.636', '-0.01318', '0.283', '-0.1638', '-0.02855', '-0.0914', '-0.3147', '0.10004', '-0.5557', '-0.04425', '-0.47', '0.07153', '-0.3826', '-0.4707', '0.03668', '-0.1389', '0.5317', '-0.1534', '0.0857', '-0.096', '0.0656', '0.296', '0.3455', '-0.8086', '0.2551', '0.608', '0.585', '0.4082', '0.3157', '-0.3142', '-0.5977', '0.1029', '-0.4866', '-0.727', '-0.337', '0.19', '0.4404', '0.23', '-0.285', '-0.1508', '-0.02153', '0.6343', '-0.3003', '0.1638', '-0.3218', '0.1422', '0.3508', '0.0362', '-0.573', '-0.3643', '0.1049', '0.004536', '-0.3394', '-0.2598', '-0.03668', '0.5625', '-0.123', '0.3489', '0.667', '-0.253', '0.658', '0.635', '-0.1094', '0.7163', '-0.379', '-0.4636', '-0.1117', '-0.10175', '-0.10913', '-0.289', '0.4966', '-0.3313', '0.366', '-0.07556', '-0.4556', '-0.3093', '0.3342', '0.11957', '-0.0984', '-0.09143', '0.627', '0.0863', '0.2593', '-0.1968', '0.6455', '0.1494', '0.404', '-0.1043', '1.072', '0.7085', '0.5356', '-0.2373', '-0.2325', '0.2196']",,,,,,,
mondo:0013935,Usher syndrome type 1J,"['Usher syndrome caused by mutation in CIB2', 'USH1J', 'USHER syndrome, type Ij', 'Usher syndrome, type 1J', 'Usher syndrome type Ij', 'CIB2 Usher syndrome']",0110836,614869,,C3553944,,,,,,H35.5,,
mondo:0013936,peroxisome biogenesis disorder 6A (Zellweger),"['peroxisome biogenesis disorder 6A (Zellweger)', 'peroxisome biogenesis disorder, complementation group 7', 'peroxisome biogenesis disorder, complementation group B', 'PBD6A']",0080481,614870,,C3553947,,C155758,,C566422,,,,
mondo:0013937,peroxisome biogenesis disorder 6B,"['peroxisome biogenesis disorder type 6B', 'peroxisome biogenesis disorder 6B', 'PBD6B']",,614871,,C3553948,,C155759,,,,,,
mondo:0013938,peroxisome biogenesis disorder 7A (Zellweger),"['peroxisome biogenesis disorder, complementation group A', 'peroxisome biogenesis disorder, complementation group 8', 'PBD7A', 'peroxisome biogenesis disorder 7A (Zellweger)']",0080482,614872,,C3888385,,,,,,,,
mondo:0013939,peroxisome biogenesis disorder 7B,"['peroxisome biogenesis disorder type 7B', 'peroxisome biogenesis disorder 7B', 'PBD7B']",,614873,,C3553951,,C155761,,,,,,
mondo:0013940,primary ciliary dyskinesia 18,"['primary ciliary dyskinesia 18 with or without situs inversus', 'DNAAF5 primary ciliary dyskinesia', 'CILD18', 'ciliary dyskinesia, primary, 18, with or without situs inversus', 'ciliary dyskinesia, primary, 18', 'ciliary dyskinesia, primary, type 18', 'primary ciliary dyskinesia caused by mutation in DNAAF5', 'primary ciliary dyskinesia type 18']",0110604,614874,,C3543825,,,,,,,,
mondo:0013941,metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria,"['spondyloenchondromatosis with D-2-hydroxyglutaric aciduria', 'metaphyseal enchondromatosis with D-2-hydroxyglutaric aciduria', 'metaphyseal Enchondrodysplasia with 2-hydroxyglutaric aciduria', 'metaphyseal chondromatosis with D-2-hydroxyglutaric aciduria']",,614875,99646,C3553958,,,,,,,,
mondo:0013942,peroxisome biogenesis disorder 8A (Zellweger),"['peroxisome biogenesis disorder, complementation group 9', 'PBD8A', 'peroxisome biogenesis disorder 8A (Zellweger)', 'peroxisome biogenesis disorder, complementation group D']",0080483,614876,,C3553959,,,,,,,,
mondo:0013943,peroxisome biogenesis disorder 8B,"['peroxisome biogenesis disorder 8B', 'peroxisome biogenesis disorder type 8B', 'PBD8B']",,614877,,C3553960,,C155763,,,,,,
mondo:0013944,autoinflammation-PLCG2-associated antibody deficiency-immune dysregulation,"['APLAID', 'autoinflammation, antibody deficiency, and immune dysregulation syndrome', 'AUTOINFLAMMATION, antibody deficiency, and immune dysregulation, PLCG2-associated']",,614878,324530,C3553961,,,,,,,,
mondo:0013945,peroxisome biogenesis disorder 9B,"['peroxisome biogenesis disorder 9B', 'peroxisome biogenesis disorder type 9B', 'PBD9B', 'peroxisome biogenesis disorder, PEX7-related, atypical', 'peroxisome biogenesis disorder, complementation group 11', 'peroxisome biogenesis disorder, complementation group R', 'Refsum disease, adult, 2']",,614879,,CN159238,,,,,,,,
mondo:0013946,hypogonadotropic hypogonadism 15 with or without anosmia,"['hypogonadotropic hypogonadism 15 with or without anosmia', 'hypogonadotropic hypogonadism caused by mutation in HS6ST1', 'HH15', 'HS6ST1 hypogonadotropic hypogonadism']",0090075,614880,,C3553977,,,,,,,,
mondo:0013947,young adult-onset distal hereditary motor neuropathy,"['Young adult-onset dHMN', 'autosomal recessive distal spinal muscular atrophy type 5', 'dSMA5', 'spinal muscular atrophy, distal, autosomal recessive, 5', 'DSMA5', 'spinal muscular atrophy, distal, autosomal recessive, type 5']",0111214,614881,314485,C3553989,"['-0.4475', '0.239', '0.191', '-0.3909', '-0.3193', '-0.468', '-0.0112', '0.75', '-0.4297', '0.2266', '0.07733', '-0.01712', '-0.347', '0.02528', '0.2291', '0.1497', '0.1443', '-0.2107', '-0.2634', '-0.601', '0.1903', '-0.2993', '0.2147', '0.5024', '0.1669', '0.2482', '-0.03836', '-0.1815', '-0.6113', '-0.2031', '0.2153', '-0.0901', '0.2842', '0.1126', '-0.0647', '-0.0948', '-0.3062', '-0.2074', '-0.1876', '-0.3372', '-0.2688', '-0.3093', '-0.3037', '0.623', '-0.0657', '-0.4497', '-0.08453', '0.336', '0.11084', '0.3706', '0.2035', '0.3638', '-0.1912', '-0.1738', '-0.01544', '-0.601', '0.4863', '-0.2491', '-0.2761', '0.1317', '0.01648', '-0.0494', '0.03137', '0.192', '-0.7417', '0.03665', '0.2029', '0.6597', '-0.10266', '0.2344', '-0.2491', '0.2957', '0.364', '-0.3186', '0.444', '0.2817', '0.1236', '0.4568', '-0.1316', '-0.3108', '0.12384', '-0.3123', '0.591', '0.615', '-0.03436', '0.1415', '-0.2194', '0.0832', '0.2178', '0.00741', '0.2666', '-0.02435', '0.2168', '0.362', '0.508', '0.2983', '0.635', '0.0787', '-0.2112', '0.3958']",,,,,,,
mondo:0013948,peroxisome biogenesis disorder 10A (Zellweger),"['peroxisome biogenesis disorder, complementation group 12', 'PBD10A', 'peroxisome biogenesis disorder 10A (Zellweger)', 'peroxisome biogenesis disorder, complementation group G']",0080484,614882,,C3553999,,,,,,,,
mondo:0013949,peroxisome biogenesis disorder 11A (Zellweger),"['peroxisome biogenesis disorder 11A (Zellweger)', 'PBD11A', 'peroxisome biogenesis disorder, complementation group 13', 'peroxisome biogenesis disorder, complementation group H']",0080485,614883,,C3554000,,,,,,,,
mondo:0013950,peroxisome biogenesis disorder 11B,"['peroxisome biogenesis disorder 11B', 'PBD11B', 'peroxisome biogenesis disorder type 11B']",,614885,,C3554001,,,,,,,,
mondo:0013951,peroxisome biogenesis disorder 12A (Zellweger),"['peroxisome biogenesis disorder, complementation group 14', 'peroxisome biogenesis disorder 12A (Zellweger)', 'Cgj', 'Cg14', 'PBD12A', 'peroxisome biogenesis disorder, complementation group J']",0080486,614886,,C3554002,,,,,,,,
mondo:0013952,peroxisome biogenesis disorder 13A (Zellweger),"['peroxisome biogenesis disorder, complementation group K', 'PBD13A', 'peroxisome biogenesis disorder 13A (Zellweger)']",0080487,614887,,C3554004,,,,C566624,,,,
mondo:0013953,immunodeficiency 28,"['primary immunodeficiency disease caused by mutation in IFNGR2', 'IFNGR2 primary immunodeficiency disease', 'immunodeficiency 28', 'immunodeficiency 28, Mycobacteriosis', 'IMD28', 'immunodeficiency type 28', 'Ifngr2 deficiency']",0111995,614889,,C4013947,"['-0.0344', '0.09076', '0.00321', '-0.0501', '0.01045', '-0.07983', '0.01909', '0.07086', '-0.0602', '-0.06445', '-0.02914', '0.02184', '-0.02444', '0.02725', '-0.000416', '-0.05438', '0.012985', '-0.02295', '-0.00316', '-0.12335', '-0.04565', '-0.02107', '0.0695', '-0.0345', '0.0323', '-0.01807', '-0.02853', '-0.01007', '-0.01633', '-0.06052', '0.067', '0.02937', '0.09863', '0.01636', '0.01241', '-0.02959', '-0.05124', '-0.03763', '-0.04858', '-0.06024', '0.02437', '-0.0726', '0.003277', '-0.04712', '-0.0162', '-0.08136', '-0.05524', '0.03366', '0.03705', '0.02629', '-0.01764', '-0.02678', '0.00686', '0.01231', '-0.0485', '0.00881', '0.0649', '-0.0796', '-0.0649', '0.0003655', '0.04022', '0.04672', '0.02386', '0.01779', '0.0004582', '0.011055', '0.06097', '0.04462', '-0.10254', '0.0823', '-0.05994', '0.004055', '0.01098', '-0.0308', '0.08936', '0.05978', '0.01888', '-0.004795', '0.03375', '-0.01015', '0.004475', '-0.008286', '-0.01236', '0.0543', '0.006573', '0.01483', '0.078', '0.04633', '0.115', '-0.0002913', '0.0176', '0.0923', '0.01012', '0.02', '0.183', '0.08527', '0.05542', '-0.1058', '-0.0128', '0.009415']",,,,,,,
mondo:0013954,Mendelian susceptibility to mycobacterial diseases due to complete IL12B deficiency,"['IL12B autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency', 'immunodeficiency 29', 'MSMD due to complete interleukin 12B deficiency', 'IL12B deficiency', 'MSMD due to complete IL12B deficiency', 'IMD29', 'Mendelian susceptibility to mycobacterial diseases due to complete interleukin 12B deficiency', 'immunodeficiency 29, mycobacteriosis', 'immunodeficiency type 29']",0111950,614890,319558,C4013948,"['-0.05902', '0.396', '-0.1422', '-0.1798', '0.04553', '-0.3245', '0.3555', '-0.275', '0.1152', '-0.6465', '-0.133', '-0.00959', '-0.2135', '0.0997', '0.334', '-0.119', '-0.305', '-0.465', '-0.2218', '-0.5986', '-0.2327', '-0.337', '0.624', '-0.544', '-0.2263', '0.0667', '-0.767', '-0.004154', '0.014465', '-0.9233', '-0.02344', '0.1484', '0.3667', '0.1566', '0.2522', '-0.619', '-0.2905', '-0.29', '-0.3096', '0.1035', '-0.2185', '-0.2112', '0.877', '-0.2737', '-0.262', '-0.04065', '-0.001901', '-0.6084', '0.1967', '0.09906', '0.4087', '-0.454', '0.5835', '-0.0688', '-0.01913', '-0.04477', '0.973', '-0.1656', '0.253', '0.49', '0.0486', '0.4949', '0.362', '0.02577', '0.562', '0.2491', '0.4285', '0.2174', '-0.01057', '0.6177', '0.2727', '-0.2795', '-0.1849', '-0.1451', '0.3467', '0.2812', '0.255', '-0.315', '-0.1985', '0.2479', '-0.331', '0.2401', '0.2041', '0.3003', '-0.1655', '0.14', '0.4844', '0.2976', '0.7695', '-0.11755', '0.1951', '0.4277', '-0.6353', '-0.3123', '0.9297', '0.9297', '0.357', '-0.4617', '0.0532', '-0.5547']",,,,,,,
mondo:0013955,Mendelian susceptibility to mycobacterial diseases due to complete IL12RB1 deficiency,"['MSMD due to complete IL12RB1 deficiency', 'IMD30', 'Mendelian susceptibility to mycobacterial infections due to IL12 deficiency', 'Mendelian susceptibility to interleukin 12 receptor beta 1 deficiency', 'immunodeficiency 30', 'IL-12Râ1 deficiency', 'MSMD due to complete interleukin 12 receptor beta 1 deficiency', 'IL12RB1 deficiency', 'IL12RB1 autosomal recessive mendelian susceptibility to mycobacterial diseases due to a complete deficiency', 'immunodeficiency type 30']",0111990,614891,319552,C4013949,"['0.2686', '0.2242', '-0.484', '-0.0719', '0.301', '-0.1539', '0.207', '-0.4084', '0.2139', '-0.991', '0.09985', '0.2798', '-0.2267', '0.2876', '0.3958', '-0.03244', '0.1235', '-0.3938', '-0.1763', '-0.377', '0.2363', '-0.03925', '0.4854', '-0.4395', '-0.3975', '0.1678', '-0.644', '0.1735', '-0.1932', '-0.338', '0.227', '0.1328', '0.5044', '0.0756', '0.3496', '-0.551', '-0.1519', '-0.613', '-0.4373', '0.00324', '0.03815', '-0.2074', '0.656', '-0.4072', '-0.2427', '0.1534', '-0.194', '-0.4448', '-0.00569', '0.714', '-0.01379', '-0.2583', '0.28', '0.2404', '-0.2244', '0.0986', '0.4404', '-0.0976', '0.11414', '0.6196', '0.3105', '0.3752', '0.453', '-0.1295', '0.4407', '0.285', '0.251', '0.3174', '-0.356', '0.617', '0.1017', '-0.581', '-0.0465', '-0.1065', '0.591', '0.3606', '0.1787', '-0.05432', '-0.3206', '0.2133', '-0.403', '0.1251', '0.2527', '0.4072', '0.0809', '0.2457', '-0.001029', '0.3374', '0.779', '-0.1598', '0.3474', '0.34', '-0.2983', '-0.2052', '1.034', '0.4656', '0.10455', '-0.6504', '0.2837', '-0.6123']",,,,,,,
mondo:0013956,Mendelian susceptibility to mycobacterial diseases due to partial STAT1 deficiency,"['Stat1 deficiency, autosomal dominant', 'IMD31A', 'STAT1 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency', 'MSMD due to partial signal transducer and activator of transcription 1 deficiency', 'MSMD due to partial STAT1 deficiency', 'Mendelian susceptibility to mycobacterial diseases due to partial signal transducer and activator of transcription 1 deficiency', 'immunodeficiency 31A', 'immunodeficiency type 31A', 'immunodeficiency 31A, Mycobacteriosis, autosomal dominant']",0111945,614892,319595,C4013950,"['0.2751', '0.2489', '0.02168', '-0.2443', '-0.0244', '-0.3386', '0.207', '-0.2087', '0.438', '-0.3713', '0.0778', '-0.0006075', '-0.4224', '-0.2418', '0.4883', '0.1991', '-0.1274', '-0.3364', '-0.2727', '-0.2023', '-0.2025', '0.3176', '0.9546', '-0.2482', '-0.587', '0.1678', '-0.362', '0.1676', '0.01663', '-0.5693', '0.1495', '-0.1492', '0.6274', '0.2406', '0.1702', '-0.4768', '-0.3662', '0.04068', '-0.4268', '-0.01826', '0.277', '-0.2328', '0.446', '-0.04584', '-0.3274', '-0.5083', '-0.2217', '-0.184', '-0.1622', '0.4033', '0.4526', '-0.5728', '0.01563', '0.01845', '-0.3218', '0.2308', '0.598', '-0.3254', '-0.1564', '0.4626', '-0.01541', '0.1786', '0.3176', '0.2327', '0.3015', '0.1544', '0.666', '0.256', '-0.3254', '0.4172', '0.3962', '-0.1315', '0.3403', '0.1033', '0.3428', '0.672', '0.4824', '0.3057', '-0.0579', '0.2861', '-0.447', '0.336', '0.3486', '0.3772', '0.1847', '0.07074', '0.5337', '0.921', '0.6753', '-0.3955', '0.724', '0.6265', '-0.1814', '-0.501', '1.233', '0.768', '0.00325', '-0.6367', '-0.0317', '-0.2568']",,,,,,,
mondo:0013957,Mendelian susceptibility to mycobacterial diseases due to partial IRF8 deficiency,"['IRF8 deficiency, autosomal dominant', 'MSMD due to partial IRF8 deficiency', 'CD11c-positive/CD1c-positive Dendritic cell deficiency, autosomal dominant', 'immunodeficiency 32A, Mycobacteriosis, autosomal dominant', 'Mendelian susceptibility to mycobacterial diseases due to partial interferon regulatory factor 8 deficiency', 'MSMD due to partial interferon regulatory factor 8 deficiency', 'immunodeficiency 32A', 'IMD32A', 'IRF8 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency', 'immunodeficiency type 32A']",0111986,614893,319600,C3808589,"['-0.11975', '0.11255', '0.09216', '-0.3418', '0.011116', '-0.48', '0.429', '0.1131', '0.2084', '-0.4026', '0.1251', '0.536', '-0.2322', '-0.0763', '0.352', '0.0522', '0.3', '-0.0811', '-0.1461', '-0.5327', '-0.2078', '-0.11743', '0.702', '-0.1036', '-0.411', '0.2144', '-0.656', '0.03415', '-0.3113', '-0.6133', '0.06433', '-0.1609', '0.6445', '0.3062', '0.1398', '-0.4556', '-0.4646', '-0.302', '-0.3464', '0.0833', '0.2861', '-0.4158', '0.555', '-0.412', '-0.2073', '-0.2517', '0.00446', '0.1544', '-0.1566', '0.395', '0.1838', '-0.4128', '0.05542', '-0.1718', '-0.0708', '0.1974', '0.353', '-0.3386', '-0.1272', '0.342', '0.2263', '0.5186', '0.4573', '-0.03937', '0.731', '0.1095', '0.10724', '0.0668', '-0.4104', '0.525', '0.1901', '-0.4917', '0.1142', '-0.2654', '0.438', '0.3445', '0.4038', '0.2957', '-0.1726', '0.4016', '-0.4963', '0.335', '0.04904', '0.5635', '-0.01572', '-0.004154', '0.2676', '0.5527', '0.833', '-0.306', '0.734', '0.569', '-0.0196', '-0.3293', '0.8027', '0.7065', '0.286', '-0.664', '-0.0572', '-0.1448']",,,,,,,
mondo:0013959,Charcot-Marie-Tooth disease type 4F,"['Prx Charcot-Marie-Tooth disease type 4', 'PRX Charcot-Marie-Tooth disease type 4', 'CMT4F', 'Charcot-Marie-Tooth disease, type 4F', 'Charcot-Marie-Tooth disease type 4 caused by mutation in Prx', 'Charcot-Marie-Tooth disease, demyelinating, type 4F']",0110193,614895,99952,C3540453,"['0.1552', '0.2461', '0.3662', '0.1884', '0.1016', '-0.1436', '0.1383', '0.729', '-0.7666', '-0.1332', '-0.00416', '0.3396', '-0.679', '0.379', '-0.06683', '-0.08307', '-0.1749', '-0.391', '-0.43', '-0.7715', '0.0594', '0.3337', '0.4329', '0.689', '0.2078', '0.3213', '0.0443', '0.2062', '0.0219', '-0.1172', '0.199', '-0.6157', '0.009964', '0.1483', '0.4421', '-0.872', '-0.598', '-0.4854', '0.4421', '-0.055', '-1.405', '-0.5137', '-0.615', '0.4668', '-0.1672', '-0.3477', '0.12115', '0.1108', '-0.2351', '0.332', '0.1461', '0.315', '-0.4158', '-0.919', '0.3025', '-0.004787', '-0.3684', '0.43', '-0.6', '-0.11865', '-0.4792', '0.1995', '0.7935', '0.7827', '-0.7915', '1.199', '-0.284', '0.7197', '-0.5205', '0.08966', '-0.4836', '0.0875', '0.4138', '-0.0628', '1.164', '0.4536', '-0.1324', '0.3762', '0.087', '-0.58', '-0.1792', '-0.361', '0.879', '0.7104', '0.03723', '-0.3386', '0.2421', '0.4949', '0.7134', '0.35', '0.473', '0.1882', '-0.06116', '0.2844', '0.3264', '0.5063', '0.4243', '-0.55', '0.08105', '0.717']",,,,,,,
mondo:0013960,sinoatrial node dysfunction and deafness,"['sinoatrial node dysfunction and deafness', 'SANDD']",,614896,324321,C3554018,"['-0.4084', '0.1418', '-0.1614', '-0.004604', '0.321', '-0.5327', '0.3503', '0.564', '-0.07324', '-0.2156', '-0.2129', '0.0926', '0.2365', '-0.337', '0.3865', '0.1617', '0.00451', '0.10223', '-0.4524', '-0.502', '0.4795', '0.1359', '0.421', '-0.003109', '0.3303', '-0.1688', '0.1656', '0.02242', '-0.11505', '0.498', '0.433', '0.753', '0.1848', '0.015045', '-0.3862', '-0.6455', '-0.1137', '0.302', '0.305', '-0.3516', '0.1179', '0.1489', '0.0613', '0.1848', '0.3499', '-0.337', '-0.2969', '0.2141', '0.7036', '0.6226', '-0.633', '0.1823', '-0.1807', '0.01593', '-0.0708', '0.04102', '0.305', '-0.4204', '0.03647', '0.1139', '0.00655', '0.3992', '0.3315', '-0.121', '-0.1257', '0.1881', '0.1123', '0.82', '-0.2437', '0.568', '-0.3313', '0.343', '0.0428', '-0.1053', '0.1254', '-0.4324', '0.49', '0.1313', '-0.1656', '-0.013245', '0.1729', '-0.4258', '0.379', '0.2683', '0.04056', '-0.3232', '0.2988', '0.3513', '0.0428', '0.6807', '0.6514', '0.05975', '0.0091', '0.3567', '0.8306', '0.4983', '0.6323', '-0.08307', '-0.365', '-0.2137']",,,,,,,
mondo:0013961,hypogonadotropic hypogonadism 16 with or without anosmia,"['hypogonadotropic hypogonadism caused by mutation in SEMA3A', 'SEMA3A hypogonadotropic hypogonadism', 'HH16', 'hypogonadotropic hypogonadism 16 with or without anosmia']",0090080,614897,,C3554021,,,,,,E23.0,,
mondo:0013962,hereditary spastic paraplegia 53,"['autosomal recessive complex spastic paraplegia caused by mutation in VPS37A', 'autosomal recessive spastic paraplegia 53', 'autosomal recessive spastic paraplegia type 53', 'VPS37A autosomal recessive complex spastic paraplegia', 'hereditary spastic paraplegia type 53', 'spastic paraplegia 53, autosomal recessive', 'SPG53']",0110805,614898,319199,C4510082,"['-0.3936', '0.4473', '0.847', '-0.667', '-0.0733', '-0.7188', '-0.422', '0.4814', '-0.697', '-0.00837', '0.1562', '0.02176', '0.2129', '-0.007313', '0.3828', '0.04108', '0.014275', '-0.4573', '0.2041', '-0.447', '0.11206', '-0.1632', '0.368', '0.05804', '-0.2367', '0.3608', '-0.05933', '-0.03958', '0.1383', '-0.4038', '-0.2145', '-0.0152', '0.127', '0.1509', '-0.269', '-0.8315', '0.1254', '0.1678', '-0.2445', '-0.692', '0.05136', '-0.3', '-0.1388', '0.735', '-0.04532', '-0.406', '-0.2578', '0.1497', '0.4006', '0.01286', '-0.3235', '0.216', '-0.1858', '-0.1606', '0.0643', '-0.548', '0.2786', '-0.371', '-0.0933', '0.445', '-0.4727', '0.3281', '0.3992', '0.08514', '0.0942', '0.04413', '-0.1148', '0.5024', '-0.5493', '0.2498', '-0.2983', '0.318', '0.411', '0.05954', '0.3596', '0.3071', '0.1771', '0.1168', '-0.2153', '-0.0433', '0.0639', '-0.4421', '0.6724', '0.6655', '-0.2476', '0.5273', '-0.0845', '0.662', '0.557', '0.5522', '0.2512', '0.4524', '0.05606', '-0.2041', '0.901', '0.5054', '0.673', '-0.2583', '0.3157', '0.372']",,,,,,,
mondo:0013963,autosomal recessive nonsyndromic hearing loss 93,"['autosomal recessive nonsyndromic deafness caused by mutation in CABP2', 'DFNB93', 'CABP2 autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive 93', 'autosomal recessive nonsyndromic deafness type 93', 'autosomal recessive deafness 93', 'deafness, autosomal recessive type 93', 'autosomal recessive nonsyndromic deafness 93']",0110537,614899,,,,,,,,,,
mondo:0013964,Diamond-Blackfan anemia 11,"['Diamond-Blackfan anemia caused by mutation in RPL26', 'Diamond-Blackfan anaemia caused by mutation in RPL26', 'Diamond-Blackfan Anemia type 11', 'Diamond-Blackfan Anaemia type 11', 'RPL26 Diamond-Blackfan anaemia', 'RPL26 Diamond-Blackfan anemia', 'Diamond-Blackfan anemia 11', 'DBA11']",0111892,614900,,C3554042,,C176920,,,,,,
mondo:0013965,lethal congenital contracture syndrome 4,"['lethal congenital contracture syndrome caused by mutation in MYBPC1', 'LCCS4', 'MYBPC1 lethal congenital contracture syndrome', 'lethal congenital contracture syndrome 4', 'lethal congenital contracture syndrome type 4']",0060654,614915,137783,C3554046,,,,,,,,
mondo:0013966,catecholaminergic polymorphic ventricular tachycardia 4,"['catecholaminergic polymorphic ventricular tachycardia caused by mutation in CALM1', 'ventricular tachycardia, catecholaminergic polymorphic, type 4', 'CALM1 catecholaminergic polymorphic ventricular tachycardia', 'catecholaminergic polymorphic ventricular tachycardia type 4', 'CVPT4', 'CPVT4', 'ventricular tachycardia, catecholaminergic polymorphic, 4']",0060678,614916,,C3554047,,,,,,I47.2,,
mondo:0013967,peroxisome biogenesis disorder 14B,"['PEX11B peroxisome biogenesis disorder', 'peroxisome biogenesis disorder 14B', 'PEX14B', 'peroxisome biogenesis disorder type 14B']",0081274,614920,,C3554055,,,,,,,,
mondo:0013968,PGM1-congenital disorder of glycosylation,"['congenital disorder of glycosylation, type It', 'CDG syndrome type It', 'phosphoglucomutase 1 deficiency', 'Pgm1 deficiency', 'CDG it', 'GSD type 14', 'phosphoglucomutase deficiency type 1', 'CDG1T', 'congenital disorder of glycosylation type 1t', 'PGM1-CDG', 'CDG-It', 'GSD 14', 'glycogen storage disease 14', 'glycogen storage disease due to phosphoglucomutase deficiency', 'type 14 glycogenosis', 'phosphoglucomutase-1 deficiency', 'GSDXIV', 'congenital disorder of glycosylation type It']",0080570,614921,319646,C2752015,"['-0.4382', '-0.2319', '-0.169', '-0.3896', '0.663', '-0.349', '0.383', '0.651', '-0.3032', '0.03674', '-0.02084', '0.2734', '0.3867', '-0.2725', '-0.3784', '0.304', '0.2283', '-0.4937', '-0.629', '-0.6436', '0.318', '-0.1841', '0.4607', '-0.252', '-0.02667', '-0.129', '0.2174', '0.1189', '0.2808', '-0.5073', '0.571', '0.235', '0.5825', '0.615', '-0.3806', '-0.2751', '-0.5645', '-0.05435', '-0.01184', '0.03818', '0.07294', '0.3687', '0.2822', '0.5693', '-0.2979', '0.0782', '0.4797', '0.3123', '-0.162', '0.5894', '-0.45', '-0.04172', '-0.0646', '0.2125', '-0.2046', '-0.583', '0.3604', '-0.7715', '0.07654', '-0.06097', '0.414', '0.607', '0.2136', '-0.1832', '-0.3496', '-0.0674', '0.2412', '0.4214', '-0.458', '-0.1841', '-0.536', '0.6885', '0.0649', '-0.06415', '0.2299', '-0.01724', '0.3901', '-0.1622', '-0.307', '0.01746', '0.3184', '-0.1995', '-0.2698', '0.07886', '0.001132', '0.2069', '0.196', '0.2598', '0.268', '-0.08563', '0.2583', '0.2458', '0.2844', '-0.2595', '1.117', '0.1855', '0.2423', '-0.1309', '-0.07367', '0.0948']",,,C567859,,,,
mondo:0013969,combined oxidative phosphorylation defect type 11,"['RMND1 combined oxidative phosphorylation deficiency', 'Encephaloneuromyopathy, infantile, due to mitochondrial translation defect', 'combined oxidative phosphorylation deficiency 11', 'combined oxidative phosphorylation deficiency type 11', 'combined oxidative phosphorylation deficiency caused by mutation in RMND1', 'COXPD11']",0111481,614922,324535,C3554067,"['-0.544', '0.2319', '0.09717', '-0.0136', '-0.0369', '-0.546', '0.1368', '0.4094', '-0.3674', '0.06247', '-0.2502', '-0.2693', '-0.1344', '-0.1252', '0.00437', '-0.2228', '0.02638', '-0.2396', '-0.231', '-0.4717', '0.3157', '-0.2556', '0.2864', '-0.00825', '0.2554', '-0.1433', '0.0178', '0.1248', '-0.001429', '-0.1656', '0.2659', '0.364', '0.6406', '0.3706', '-0.02376', '-0.4438', '-0.1886', '-0.1632', '-0.3286', '0.01555', '0.086', '-0.1031', '0.01389', '0.2986', '-0.4514', '-0.2482', '0.0641', '-0.05356', '-0.187', '0.0883', '-0.2332', '-0.07465', '-0.03586', '-0.2029', '-0.144', '-0.2234', '0.2605', '-0.002174', '0.0648', '0.293', '0.07886', '0.04477', '0.3994', '-0.1292', '-0.1985', '0.04333', '0.1594', '0.4478', '-0.4976', '0.1686', '-0.2307', '0.2179', '0.1635', '-0.1311', '0.07886', '-0.1616', '0.348', '-0.1951', '-0.03705', '0.3315', '0.1083', '0.0078', '-0.0969', '0.2988', '0.2737', '-0.04205', '0.1986', '0.426', '0.3118', '0.3464', '0.5786', '0.2416', '-0.0704', '-0.0424', '0.721', '0.413', '0.4673', '-0.3003', '0.3494', '0.0204']",,,,,,,
mondo:0013970,branched-chain keto acid dehydrogenase kinase deficiency,"['branched-chain KETO acid dehydrogenase KINASE deficiency', 'branched-chain keto acid dehydrogenase kinase deficiency', 'BCKDKD', 'autism - epilepsy syndrome due to branched chain ketoacid dehydrogenase kinase deficiency', 'BCKDK deficiency', 'Bckdk deficiency']",0090126,614923,308410,C3554078,"['-0.529', '0.46', '0.2966', '-0.318', '0.2306', '-0.4136', '-0.0694', '0.4146', '-0.1857', '-0.2563', '-0.2103', '0.09985', '0.2186', '-0.578', '0.08026', '-0.2242', '0.0689', '0.1381', '-0.4514', '-0.7666', '0.10126', '-0.2434', '0.4878', '0.128', '0.01028', '-0.2112', '0.1715', '-0.2229', '-0.11676', '-0.2556', '-0.002272', '0.1542', '0.528', '0.4192', '-0.2476', '-0.459', '0.02225', '-0.0924', '-0.1793', '-0.5225', '0.1863', '-0.705', '-0.0969', '-0.3074', '-0.5454', '-0.679', '0.3586', '0.3254', '0.1168', '0.3694', '-0.1024', '-0.1786', '-0.0877', '-0.2651', '-0.03876', '0.1137', '0.2137', '-0.1686', '-0.06805', '0.2876', '0.0729', '0.00797', '0.6084', '-0.1682', '-0.010635', '0.092', '0.3088', '0.0986', '-0.491', '-0.2554', '-0.10565', '0.1724', '-0.3127', '0.06125', '0.161', '0.2021', '0.4321', '-0.251', '-0.07556', '0.1026', '0.1384', '0.4077', '-0.2576', '0.3345', '0.135', '0.1813', '-0.2678', '0.1211', '0.4944', '0.01561', '0.3206', '0.315', '-0.3806', '-0.2296', '0.383', '0.555', '0.0907', '-0.4812', '-0.04388', '0.3826']",,,,,,,
mondo:0013971,leukoencephalopathy-thalamus and brainstem anomalies-high lactate syndrome,"['combined oxidative phosphorylation defect type 12', 'combined oxidative phosphorylation deficiency caused by mutation in EARS2', 'combined oxidative phosphorylation deficiency type 12', 'combined oxidative phosphorylation deficiency 12', 'leukoencephalopathy with thalamus and brainstem involvement and high lactate', 'COXPD12', 'LTBL', 'EARS2 combined oxidative phosphorylation deficiency']",0111493,614924,314051,C3554079,"['-0.1907', '0.4543', '-0.4622', '0.1183', '0.05334', '-0.2322', '-0.229', '0.696', '-0.5537', '0.389', '-0.8403', '0.1459', '0.575', '-0.5684', '0.394', '0.04672', '0.318', '-0.3389', '-0.484', '-0.7793', '0.1124', '-0.3447', '0.354', '-0.03522', '0.5356', '0.0002252', '-0.0001128', '0.4492', '-0.5674', '0.03906', '0.789', '0.5903', '0.621', '0.2261', '0.04572', '0.6553', '-1.008', '-0.09283', '0.1819', '-0.3005', '0.1846', '-0.2742', '0.11035', '-0.2103', '0.02507', '0.11383', '0.2167', '0.05853', '-0.1606', '0.1257', '0.04047', '0.3213', '-0.5903', '-0.2969', '-0.1172', '-0.1186', '-0.139', '-0.1985', '0.02917', '0.01895', '-0.02792', '0.2961', '0.3716', '-0.5425', '-0.2471', '0.2058', '1.14', '0.1604', '-0.8877', '0.3108', '-0.2534', '0.4019', '0.05246', '-0.2329', '0.1764', '-0.1609', '0.327', '0.2722', '0.1986', '0.3098', '0.11554', '0.266', '0.02391', '0.296', '-0.1495', '0.03168', '-0.3257', '0.661', '0.308', '0.4622', '0.0775', '0.876', '0.1515', '0.1236', '-0.0658', '0.4414', '0.3318', '-0.587', '-0.1484', '0.2534']",,,,,,,
mondo:0013972,Perrault syndrome 2,"['PRLTS2', 'Perrault syndrome caused by mutation in HARS2', 'Perrault syndrome 2', 'Perrault syndrome type 2', 'HARS2 Perrault syndrome']",,614926,642976,C3554105,,,,,,,,
mondo:0013973,"ectodermal dysplasia 5, hair/nail type","['ECTD5', 'ectodermal dysplasia 5, hair/nail type']",0111657,614927,,C3554108,,,,,,,,
mondo:0013974,"ectodermal dysplasia 6, hair/nail type","['ectodermal dysplasia 6, hair/nail type', 'ECTD6']",0111659,614928,,C3554111,,,,,,,,
mondo:0013975,"ectodermal dysplasia 7, hair/nail type","['ECTD7', 'ectodermal dysplasia 7, hair/nail type', 'KRT74 pure hair and nail ectodermal dysplasia', 'pure hair and nail ectodermal dysplasia caused by mutation in KRT74']",0111660,614929,,C3554117,,,,,,,,
mondo:0013976,"ectodermal dysplasia 9, hair/nail type","['pure hair and nail ectodermal dysplasia caused by mutation in HOXC13', 'HOXC13 pure hair and nail ectodermal dysplasia', 'ectodermal dysplasia 9, hair/nail type', 'ECTD9']",0111656,614931,,C3554127,,,,,,,,
mondo:0013977,combined oxidative phosphorylation defect type 13,"['combined oxidative phosphorylation deficiency type 13', 'combined oxidative phosphorylation deficiency 13', 'COXPD13', 'combined oxidative phosphorylation deficiency caused by mutation in PNPT1', 'PNPT1 combined oxidative phosphorylation deficiency']",0111467,614932,319514,C3554129,"['-0.5415', '0.3835', '0.10046', '-0.1917', '-0.102', '-0.922', '0.2832', '0.698', '-0.633', '0.007305', '-0.3008', '-0.05594', '-7.48e-05', '-0.3508', '0.184', '-0.03302', '0.3296', '-0.3735', '-0.03735', '-0.9233', '0.2255', '-0.2832', '0.3152', '0.09625', '0.1128', '-0.02657', '-0.1407', '0.3586', '-0.582', '-0.1735', '0.116', '0.8843', '0.631', '0.199', '-0.0885', '-0.3025', '0.4036', '0.018', '-0.09717', '-0.0414', '0.392', '-0.2202', '-0.3125', '0.4385', '-0.566', '-0.1284', '-0.2546', '0.3887', '0.1904', '0.4727', '-0.2898', '0.0831', '-0.42', '-0.3606', '0.03784', '-0.4946', '0.1924', '-0.3125', '0.07214', '0.3936', '-0.007244', '0.11884', '0.7334', '-0.0393', '-0.4062', '-0.07513', '0.5605', '0.2372', '-0.3918', '0.2438', '-0.1248', '0.3628', '0.1383', '-0.0517', '0.394', '-0.1631', '0.264', '-0.07825', '-0.38', '0.3123', '-0.04813', '-0.1181', '0.265', '0.0808', '-0.05194', '-0.01834', '0.1976', '0.31', '0.6636', '-0.02092', '0.1827', '0.4963', '-0.0735', '0.2722', '0.3772', '0.572', '0.2588', '-0.12213', '0.2522', '0.1792']",,,,,,,
mondo:0013978,autosomal recessive nonsyndromic hearing loss 70,"['deafness, autosomal recessive 70', 'DFNB70', 'autosomal recessive deafness 70', 'autosomal recessive nonsyndromic deafness caused by mutation in PNPT1', 'PNPT1 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 70', 'deafness, autosomal recessive type 70', 'autosomal recessive nonsyndromic deafness 70']",0110521,614934,,C1824925,,,,,,,,
mondo:0013979,primary ciliary dyskinesia 19,"['primary ciliary dyskinesia caused by mutation in LRRC6', 'ciliary dyskinesia, primary, 19', 'CILD19', 'primary ciliary dyskinesia type 19', 'ciliary dyskinesia, primary, 19, with or without situs inversus', 'ciliary dyskinesia, primary, type 19', 'primary ciliary dyskinesia 19 with or without situs inversus', 'LRRC6 primary ciliary dyskinesia']",0110608,614935,,C3543826,,,,,,,,
mondo:0013980,"palmoplantar keratoderma, punctate type ib","['palmoplantar keratoderma, punctate type IB', 'keratoderma, palmoplantar, punctate type IB', 'PPKP1B']",,614936,,C3554145,,,,,,,,
mondo:0013981,"myoclonus, familial","['familial myoclonus', 'familial cortical myoclonus', 'myoclonus, familial cortical', 'FCM']",,,319189,C3539916,"['0.3262', '0.01067', '-0.9316', '-0.2344', '-0.741', '-0.08746', '0.2925', '-0.077', '-1.052', '-0.187', '-0.0956', '-0.10004', '-0.02895', '-0.0934', '0.564', '-0.2744', '-0.2524', '-0.387', '-0.4429', '-1.505', '-0.208', '-0.6216', '-0.615', '-0.1079', '0.1963', '-0.1578', '-0.4639', '-0.6855', '-0.225', '0.04474', '-0.0412', '0.327', '-0.003101', '-0.3916', '0.409', '-0.347', '-1.019', '-0.0621', '-0.03506', '-0.2566', '0.1343', '-0.10754', '0.4243', '-0.2402', '0.148', '-0.5234', '-0.3604', '0.143', '0.0884', '0.2393', '0.1469', '0.9756', '0.2861', '-0.05923', '0.1499', '-0.72', '-0.1072', '-0.1898', '-0.2915', '-0.2832', '0.1418', '-0.2908', '0.6416', '-0.9053', '-1.018', '0.7793', '0.803', '0.312', '-0.556', '-0.1638', '-0.4465', '0.7305', '0.493', '-0.0989', '0.0869', '0.591', '0.4382', '0.6245', '0.08234', '0.05615', '-0.05643', '-0.2847', '0.1318', '-0.08453', '0.1758', '-0.1324', '0.6255', '-0.18', '0.892', '0.607', '-0.4485', '0.0364', '-0.3943', '0.566', '0.2236', '0.133', '0.2036', '-0.2032', '0.683', '0.5044']",,,,,,,
mondo:0013982,"ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant","['ectodermal dysplasia 11A, hypohidrotic/hair/tooth type, autosomal dominant', 'ECTD11A', 'ectodermal dysplasia, hypohidrotic, autosomal dominant']",0111653,614940,,C3541517,,,,,,,,
mondo:0013983,"ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive","['ectodermal dysplasia, anhidrotic', 'ectodermal dysplasia 11B, hypohidrotic/hair/tooth type, autosomal recessive', 'ectodermal dysplasia, hypohidrotic', 'ECTD11B']",0111654,614941,,C3539920,,,,,,,,
mondo:0013984,autosomal recessive nonsyndromic hearing loss 84B,"['deafness, autosomal recessive 84b', 'deafness, autosomal recessive type 84B', 'DFNB84B', 'autosomal recessive nonsyndromic deafness 84B', 'autosomal recessive nonsyndromic deafness caused by mutation in OTOGL', 'autosomal recessive deafness 84B', 'autosomal recessive nonsyndromic deafness type 84B', 'deafness, autosomal recessive 84B', 'OTOGL autosomal recessive nonsyndromic deafness']",0110530,614944,,C3554159,,,,,,,,
mondo:0013985,autosomal recessive nonsyndromic hearing loss 18B,"['autosomal recessive deafness 18B', 'autosomal recessive nonsyndromic deafness type 18B', 'autosomal recessive nonsyndromic deafness caused by mutation in OTOG', 'deafness, autosomal recessive 18B', 'deafness, autosomal recessive type 18B', 'deafness, autosomal recessive 18b', 'DFNB18B', 'OTOG autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness 18B']",0110474,614945,,C3554163,,,,,,,,
mondo:0013986,combined oxidative phosphorylation defect type 14,"['COXPD14', 'combined oxidative phosphorylation deficiency caused by mutation in FARS2', 'combined oxidative phosphorylation deficiency 14', 'FARS2 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency type 14']",0111477,614946,319519,C3554168,"['-0.4812', '0.12085', '0.03915', '-0.1232', '0.0575', '-0.691', '-0.1423', '0.361', '-0.3115', '-0.07135', '-0.3203', '-0.2646', '0.1578', '0.01863', '0.04776', '-0.1484', '0.1953', '-0.1058', '-0.1671', '-0.5874', '0.2125', '-0.321', '0.2057', '-0.1569', '0.05515', '-0.1437', '0.05106', '0.2466', '-0.11865', '-0.1923', '0.1658', '0.5435', '0.461', '0.3748', '-0.0409', '-0.344', '0.03473', '-0.0965', '-0.251', '0.02077', '0.1655', '0.00481', '-0.04263', '0.2366', '-0.503', '-0.3586', '0.02562', '-0.01822', '-0.11774', '0.05386', '-0.3555', '-0.3003', '-0.06165', '0.07513', '-0.2896', '-0.2905', '0.04938', '0.0456', '-0.311', '0.3801', '0.0769', '0.09204', '0.4722', '-0.2834', '-8.106e-05', '0.1567', '0.3425', '0.1089', '-0.4668', '0.1602', '-0.1274', '0.06244', '-0.02643', '-0.294', '0.1919', '-0.0317', '0.2439', '-0.3577', '-0.2015', '0.4788', '0.05365', '-0.02272', '-0.1159', '0.003017', '0.07764', '-0.04926', '0.3784', '0.5044', '0.403', '0.0851', '0.3354', '0.2812', '0.01643', '-0.1421', '0.583', '0.6987', '0.1605', '-0.263', '0.5024', '-0.0349']",,,,,,,
mondo:0013987,combined oxidative phosphorylation defect type 15,"['combined oxidative phosphorylation deficiency 15', 'MTFMT combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency type 15', 'COXPD15', 'combined oxidative phosphorylation deficiency caused by mutation in MTFMT']",0111491,614947,319524,C3554182,"['-1.089', '0.312', '0.161', '0.02638', '0.2096', '-0.72', '-0.07294', '0.8457', '-0.4092', '-0.07294', '-0.5757', '-0.1951', '-0.02844', '-0.2563', '0.3572', '-0.4143', '0.3555', '-0.192', '-0.531', '-0.4988', '0.439', '-0.2795', '0.002563', '0.4075', '-0.1404', '-0.266', '-0.05432', '0.1683', '-0.286', '0.03564', '0.3833', '0.3525', '0.7295', '0.2854', '0.187', '-0.2688', '-0.1416', '0.2773', '-0.2637', '-0.04666', '0.216', '-0.0739', '-0.071', '0.3413', '-0.5176', '-0.2417', '0.226', '0.1768', '0.213', '-0.0829', '-0.347', '0.10443', '-0.5254', '-0.05963', '0.02916', '-0.05637', '0.0438', '-0.1918', '0.063', '0.4604', '0.1566', '0.2319', '0.5576', '0.4646', '-0.502', '0.2527', '0.1777', '0.656', '-0.4714', '0.3442', '-0.4075', '0.1807', '0.02383', '0.02254', '0.4043', '-0.3472', '0.519', '-0.0954', '-0.0984', '0.6377', '-0.1278', '-0.3333', '0.1296', '0.5376', '0.2307', '-0.00665', '0.2937', '0.005836', '0.5913', '0.2598', '0.3108', '0.3735', '0.124', '-0.1234', '0.5264', '-0.0852', '0.315', '-0.1658', '0.411', '0.291']",,,,,,,
mondo:0013988,"congenital heart defects, multiple types, 3","['CHTD3', 'congenital heart defects, multiple types, with Cardiac rhythm and conduction disturbances', 'congenital heart defects, multiple types, 3']",,614954,,C3554194,,,,,,,,
mondo:0013989,"developmental and epileptic encephalopathy, 14","['epileptic encephalopathy, early infantile, 14', 'developmental and epileptic encephalopathy 14', 'epileptic encephalopathy, early infantile, type 14', 'EIEE14', 'DEE14', 'KCNT1 early infantile epileptic encephalopathy', 'early infantile epileptic encephalopathy caused by mutation in KCNT1']",0080439,614959,,C3554195,,,,,,,,
mondo:0013990,pontocerebellar hypoplasia type 8,"['pontocerebellar hypoplasia due to CHMP1A mutation', 'PCH8', 'CHMP1A non-syndromic pontocerebellar hypoplasia', 'non-syndromic pontocerebellar hypoplasia caused by mutation in CHMP1A', 'pontocerebellar hypoplasia, type 8']",0060277,614961,324569,C3554209,"['-0.894', '-0.1847', '0.5815', '-0.2479', '0.263', '-0.6494', '-0.391', '0.668', '-0.9214', '-0.3792', '-0.558', '-0.912', '-0.3184', '-0.7427', '0.4539', '0.01527', '0.1148', '-0.889', '-0.1527', '-1.097', '-0.0949', '-0.01709', '0.393', '-0.02896', '0.07007', '0.2698', '0.1586', '0.2114', '0.0997', '0.0608', '0.1611', '0.02977', '0.241', '-0.1353', '-0.6284', '0.0573', '-0.146', '-0.098', '0.1097', '-0.352', '0.3333', '-0.3782', '-0.1833', '0.4312', '-0.435', '0.5034', '-0.5522', '-0.01651', '0.9927', '0.1964', '-0.0272', '-0.3328', '-0.3135', '0.05078', '-0.73', '0.09436', '0.2556', '-0.4543', '0.00819', '0.9263', '-0.3643', '0.2479', '0.2688', '0.0566', '-0.7705', '-0.0598', '0.0856', '0.2137', '-0.6626', '0.726', '0.2029', '0.2443', '-0.4282', '-0.1732', '0.0522', '0.004738', '0.3625', '0.0632', '-0.2632', '-0.2323', '-0.2058', '0.02544', '0.5063', '0.637', '-0.4165', '0.673', '-0.5938', '0.759', '0.866', '0.3127', '-0.3018', '0.323', '-0.1472', '0.5713', '0.6514', '0.5786', '0.5454', '0.1727', '0.0965', '-0.0811']",,,,,,,
mondo:0013991,obesity due to congenital leptin deficiency,"['leptin deficiency or dysfunction', 'obesity, morbid, due to leptin deficiency', 'obesity, morbid, nonsyndromic 1', 'LEPD']",0111334,614962,66628,C3554224,"['-0.314', '0.3154', '-0.301', '0.8936', '-0.0809', '-0.7983', '0.259', '0.7803', '-0.2471', '-0.6323', '-0.1514', '0.3767', '0.1829', '0.1971', '-0.794', '-0.5034', '-0.259', '0.959', '-0.844', '-0.692', '0.1232', '-0.4521', '0.3774', '-0.3086', '0.3113', '0.355', '-0.3325', '-0.7026', '-0.0365', '-0.3245', '0.4736', '-0.5254', '0.4285', '0.0208', '-0.02698', '-0.5825', '-0.846', '0.188', '0.3806', '-0.08136', '-0.05295', '-0.26', '-0.769', '0.3186', '-0.00398', '-0.681', '0.517', '-0.1353', '0.4355', '0.04355', '-0.4949', '0.05722', '0.616', '-0.02359', '-0.426', '0.7993', '-0.3057', '-0.1881', '-0.1477', '-0.4878', '0.4368', '0.321', '-0.2607', '-0.6504', '-0.00107', '0.746', '-0.526', '0.3906', '0.4976', '0.422', '0.2074', '0.3079', '-0.04636', '-0.3396', '0.6357', '-0.8867', '-0.2803', '-0.05637', '-1.189', '0.721', '-0.1493', '1.033', '-0.008286', '0.2189', '0.9624', '0.561', '0.3105', '0.3064', '0.971', '0.433', '-0.10004', '0.3481', '-0.2365', '0.587', '0.5576', '0.2585', '0.16', '-0.3577', '-0.2195', '-0.00998']",,,,,,,
mondo:0013992,obesity due to leptin receptor gene deficiency,"['obesity, morbid, due to leptin receptor deficiency', 'leptin receptor deficiency', 'obesity, morbid, nonsyndromic 2']",,614963,179494,C3554225,"['-0.2588', '0.3726', '0.003458', '0.919', '-0.2866', '-0.745', '0.08527', '0.614', '-0.3286', '-0.6846', '0.0889', '0.2664', '0.1638', '0.3547', '-0.738', '-0.678', '-0.4753', '0.8535', '-0.7905', '-0.7583', '0.03754', '-0.3186', '0.2277', '-0.2041', '0.1758', '0.186', '-0.4104', '-0.5073', '0.2479', '-0.3608', '0.3594', '-0.3916', '0.3103', '0.11566', '-0.0824', '-0.514', '-0.83', '0.1731', '0.5356', '-0.0587', '0.0708', '-0.2798', '-0.71', '0.3687', '0.1266', '-0.7466', '0.589', '-0.03894', '0.5273', '0.03708', '-0.4817', '-0.1812', '0.5933', '-0.1063', '-0.3477', '0.715', '-0.003353', '-0.003952', '-0.0055', '-0.487', '0.631', '0.4143', '-0.2267', '-0.738', '-0.18', '0.803', '-0.477', '0.388', '0.3752', '0.4573', '0.2083', '0.4397', '-0.1499', '-0.2502', '0.598', '-0.501', '-0.09045', '-0.0608', '-1.229', '0.622', '0.0534', '1.055', '0.1304', '0.1356', '0.9976', '0.5015', '0.4048', '0.2727', '1.018', '0.4365', '-0.2522', '0.2932', '-0.1472', '0.6597', '0.694', '0.1345', '0.221', '-0.3848', '-0.4087', '0.0751']",C120386,,,,,,
mondo:0013993,pontocerebellar hypoplasia type 7,"['pontocerebellar hypoplasia-46,XY disorder of sex development syndrome', 'PCH7', 'non-syndromic pontocerebellar hypoplasia caused by mutation in TOE1', 'pontocerebellar hypoplasia, type 7', 'TOE1 non-syndromic pontocerebellar hypoplasia']",0060276,614969,284339,C3554226,"['-0.7036', '0.002535', '-0.2883', '-0.1417', '0.1393', '-1.113', '-0.1121', '0.1974', '-1.227', '-0.2361', '-0.903', '-0.812', '-0.6494', '-0.2856', '0.5703', '-0.2827', '0.7417', '-0.2122', '0.05612', '-1.1455', '-0.1709', '-0.4253', '1.058', '-0.8813', '0.2188', '-0.08563', '-0.09216', '0.1279', '0.1775', '-0.63', '0.3408', '0.3232', '0.2878', '-0.05566', '-0.511', '0.2013', '-0.2354', '0.02179', '-0.4272', '0.2976', '0.81', '-0.1935', '-0.1957', '0.0915', '-0.1075', '-0.4272', '-0.497', '0.0358', '-0.10144', '0.658', '-0.1296', '-0.5864', '-0.7935', '0.2603', '0.1736', '-0.175', '0.2563', '-0.512', '-0.1587', '0.785', '-0.0874', '0.2896', '0.7134', '0.1088', '-0.09344', '-0.05356', '0.63', '0.2361', '-0.737', '0.737', '-0.02051', '0.4163', '0.1656', '-0.01248', '-0.3442', '-0.2179', '-0.1793', '-0.3232', '-0.947', '-0.2515', '0.1011', '0.902', '-0.0816', '0.2295', '0.2008', '0.1453', '-0.3994', '0.04932', '0.673', '-0.5522', '-0.1232', '0.4202', '-0.3123', '0.1044', '0.84', '-0.07526', '0.06107', '-0.094', '0.5273', '-0.1923']",,,,,,,
mondo:0013994,Joubert syndrome 20,"['TMEM231 Joubert syndrome', 'Joubert syndrome 20', 'Joubert syndrome caused by mutation in TMEM231', 'Joubert syndrome type 20', 'JBTS20']",0110989,614970,,C3554235,,,,,,,,
mondo:0013995,"cholestasis, intrahepatic, of pregnancy, 3","['ICP3', 'cholestasis, intrahepatic, of pregnancy type 3', 'cholestasis, intrahepatic, of pregnancy 3']",0070229,614972,,C3554241,"['-0.04013', '0.1109', '0.0374', '-0.0418', '0.02089', '-0.1786', '0.0452', '0.11053', '-0.0998', '0.00869', '-0.1462', '0.01051', '-0.02583', '0.05444', '-0.1373', '-0.148', '0.0278', '-0.03275', '0.01043', '-0.2139', '-0.08765', '-0.0785', '0.1552', '-0.02509', '-0.01888', '-0.03625', '0.03604', '0.014786', '-0.002373', '-0.08', '0.1598', '0.005455', '0.1705', '0.1122', '-0.0724', '-0.1051', '-0.06174', '-0.0135', '-0.0502', '-0.03168', '-0.00673', '-0.0797', '0.06097', '0.00377', '-0.03174', '-0.0243', '-0.02013', '0.0734', '0.01231', '0.0731', '-0.03357', '-0.0343', '0.0545', '-0.01482', '-0.01799', '0.00898', '0.1042', '-0.1172', '-0.1561', '0.01032', '0.07947', '0.0816', '0.1077', '-0.02591', '-0.00911', '-0.00434', '0.1785', '0.07336', '-0.07666', '0.1228', '0.0248', '0.04053', '0.06647', '-0.09625', '0.03162', '0.06726', '0.0699', '-0.03525', '-0.10736', '-0.05118', '-0.00989', '0.038', '-0.073', '0.05914', '-0.0244', '-0.01058', '0.04895', '0.1007', '0.1566', '-0.0569', '0.1175', '0.1293', '-0.02899', '-0.0276', '0.2072', '0.05176', '0.10583', '-0.1161', '-0.01564', '-0.01949']",,0009150,,,,,
mondo:0013996,focal facial dermal dysplasia type II,"['Brauer-Setleis syndrome', 'FFDD type II', 'FFDD2', 'focal facial dermal dysplasia 2, Brauer-Setleis type']",,614973,398173,C3554245,,,,,,,,
mondo:0013997,focal facial dermal dysplasia type IV,"['focal facial dermal dysplasia 4', 'focal Facial dermal dysplasia type 4', 'FFDD4', 'focal facial preauricular dysplasia', 'FFDD type IV']",,614974,398189,C3554246,"['0.268', '0.4827', '-0.1522', '-0.0912', '0.1433', '-0.02963', '-0.02446', '-0.0695', '-0.03424', '-0.2532', '-0.3699', '-0.171', '-0.0659', '-0.1985', '-0.05774', '0.6294', '0.2683', '-0.9297', '-0.03036', '-0.772', '-0.007713', '0.4146', '0.7207', '0.08374', '0.3223', '0.2396', '-0.23', '-0.0756', '0.2002', '0.0978', '0.579', '-0.28', '0.1351', '-0.216', '-0.03497', '-0.2157', '-0.094', '-0.6235', '-0.010796', '-0.05692', '-0.10486', '-0.662', '0.1201', '-0.05234', '-0.02213', '0.1588', '-0.3013', '0.586', '0.0401', '-0.3716', '0.02861', '-0.2385', '0.014854', '0.1218', '-1.028', '-0.1863', '0.1923', '0.1593', '-0.573', '0.3862', '0.3894', '0.11346', '-0.05252', '-0.2202', '-0.3845', '0.05667', '0.2335', '0.1804', '-0.1809', '0.769', '-0.298', '-0.4019', '0.4067', '0.01421', '0.0755', '-0.2349', '0.1318', '-0.2463', '-0.2527', '-0.1392', '0.1637', '-0.1759', '0.335', '0.0911', '0.126', '-0.369', '0.06238', '1.161', '0.3154', '0.2324', '0.1707', '0.3706', '0.2242', '0.6104', '0.9243', '-0.1901', '0.3787', '-0.5967', '0.475', '0.688']",,,,,,,
mondo:0013998,MEGF8-related Carpenter syndrome,"['Carpenter syndrome caused by mutation in MEGF8', 'CARPENTER syndrome 2', 'MEGF8 Carpenter syndrome', 'CRPT2', 'Carpenter syndrome type 2', 'Carpenter syndrome 2']",,614976,,C3554247,,,,,,,,
mondo:0013999,optic nerve edema-splenomegaly syndrome,"['splenomegaly, cytopenia, and vision loss', 'ROSAH syndrome']",,614979,313800,C3554278,,,,,,,,
mondo:0014000,"congenital heart defects, multiple types, 2","['congenital heart defects, multiple types, 2', 'congenital heart defects, nonsyndromic, 2', 'TAB2 congenital heart malformation', 'congenital heart malformation caused by mutation in TAB2', 'CHTD2']",,614980,,C3554279,,,,,,,,
mondo:0014001,Usher syndrome type 1K,"['USH1K', 'Usher syndrome type IK', 'USHER syndrome, type IK']",0110837,614990,,C3539124,,,,,,H35.5,,
mondo:0014002,autosomal dominant nocturnal frontal lobe epilepsy 5,"['autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in KCNT1', 'epilepsy nocturnal frontal lobe, 5', 'ENFL5', 'KCNT1 autosomal dominant nocturnal frontal lobe epilepsy', 'epilepsy, nocturnal frontal lobe, type 5', 'nocturnal frontal lobe epilepsy 5', 'epilepsy, nocturnal frontal lobe, 5', 'autosomal dominant nocturnal frontal lobe epilepsy type 5']",0060686,615005,,C3554306,,,,,,,,
mondo:0014003,"developmental and epileptic encephalopathy, 15","['developmental and epileptic encephalopathy 15', 'EIEE15', 'DEE15', 'epileptic encephalopathy, early infantile, type 15', 'epileptic encephalopathy, early infantile, 15']",0080414,615006,,C3554316,,,,,,,,
mondo:0014004,"basal ganglia calcification, idiopathic, 4","['IBGC4', 'basal ganglia calcification, idiopathic, 4', 'basal ganglia calcification, idiopathic, type 4']",,615007,,C3554321,,,,,,,,
mondo:0014005,immunoglobulin-mediated membranoproliferative glomerulonephritis,"['Mesangiocapillary glomerulonephritis type 1', 'Ahus, susceptibility to, 7', 'membranoproliferative glomerulonephritis type I', 'Ig-mediated membranoproliferative glomerulonephritis', 'nephrotic syndrome, type 7, with membranoproliferative glomerulonephritis', 'nephrotic syndrome, type 7', 'NPHS7', 'Ig-mediated MPGN', 'immune Complex mediated membranoproliferative glomerulonephritis', 'Immunoglobulin-mediated MPGN', 'hemolytic uremic syndrome, atypical, susceptibility to, 7']",,615008,329903,,"['0.5728', '0.4265', '-0.3447', '0.424', '-0.10223', '-0.505', '0.1826', '-0.05365', '-0.503', '-0.1349', '0.2037', '-0.03375', '-0.385', '1.139', '-0.05856', '-0.2944', '-0.2708', '0.503', '0.589', '0.08167', '-0.1576', '-0.966', '0.7373', '0.05658', '0.719', '-0.2368', '-0.9287', '0.855', '0.1053', '-0.216', '0.05664', '0.329', '0.6006', '0.01339', '-0.0766', '-0.05322', '-0.41', '0.7466', '0.334', '-0.619', '-0.4963', '-0.1757', '-0.2322', '-0.3918', '0.1896', '-0.3677', '-0.4536', '-0.3914', '-0.1991', '-0.04263', '0.2037', '0.1254', '1.191', '-0.3706', '-0.708', '-0.2169', '0.04504', '-0.00887', '-0.9185', '-0.5796', '-0.7085', '0.0862', '-0.10834', '-0.1794', '-0.1304', '-0.3767', '0.3376', '0.4355', '-0.7144', '0.702', '-0.817', '0.3008', '0.565', '-0.2426', '-0.1357', '0.1263', '0.609', '1.255', '-0.1593', '0.4797', '-0.343', '0.2109', '-0.01656', '0.2236', '0.02771', '-0.2798', '0.04858', '-0.4832', '0.1677', '1.048', '0.8174', '0.2412', '-0.4546', '0.2737', '0.7646', '0.7954', '-0.1835', '-0.844', '-0.7954', '-0.0256']",C123055,,,,,,
mondo:0014006,Schuurs-Hoeijmakers syndrome,"['mental retardation, autosomal dominant type 17', 'Schuurs-Hoeijmakers syndrome', 'mental retardation, autosomal dominant 17', 'intellectual disability, autosomal dominant 17', 'autosomal dominant mental retardation 17', 'autosomal dominant intellectual disability 17', 'PACS1-related syndrome', 'intellectual disability, autosomal dominant type 17', 'SHMS', 'intellectual disability-craniofacial dysmorphism-cryptorchidism syndrome', 'autosomal dominant intellectual disability-17', 'MRD17']",0070047,615009,329224,C3554343,"['0.08', '0.2046', '0.4934', '-0.4836', '0.12305', '-0.1754', '0.1753', '0.5767', '-0.764', '-0.4043', '-0.002058', '-0.1333', '0.371', '-0.394', '0.0612', '0.1947', '0.2258', '-0.3723', '-0.2812', '-0.3767', '0.1818', '0.2632', '0.2091', '-0.0639', '0.5327', '-0.511', '-0.2101', '0.1572', '0.549', '-0.1704', '0.1906', '-0.02948', '0.3066', '0.0655', '0.2429', '-0.0856', '-0.1523', '-0.2246', '-0.1876', '-0.727', '0.3442', '-0.135', '-0.2329', '0.004272', '-0.07404', '-0.495', '0.1469', '0.4146', '0.07733', '-0.1107', '-0.4126', '0.04053', '-0.2986', '-0.02754', '-0.1884', '-0.3162', '0.1738', '0.1829', '-0.04672', '0.4038', '-0.1084', '0.1622', '0.2423', '0.0525', '0.1338', '-0.0691', '0.1076', '0.04483', '-0.0662', '0.2314', '-0.339', '0.4275', '0.06', '0.2346', '-0.261', '0.1267', '0.631', '-0.07196', '-0.3945', '0.2544', '0.346', '-0.1858', '0.1877', '0.5825', '0.2122', '0.1792', '-0.3137', '0.0883', '0.3083', '0.6455', '-0.0881', '0.543', '0.2234', '0.1691', '0.828', '0.4185', '0.2524', '-0.484', '0.3616', '0.2466']",C150555,,,,,,
mondo:0014007,Aicardi-Goutieres syndrome 6,"['Adar Aicardi-Goutieres syndrome', 'ADAR Aicardi-Goutieres syndrome', 'Aicardi-Goutieres syndrome caused by mutation in Adar', 'Aicardi-Goutieres syndrome 6', 'AGS6', 'Aicardi-Goutieres syndrome type 6']",,615010,,C3539013,,,,,,,,
mondo:0014008,phosphohydroxylysinuria,"['Phosphohydroxylysinuria', 'phosphohydroxylysinuria', 'PHLU', 'PHOSPHOHYDROXYLYSINURIA']",,615011,,C3554344,"['-0.009056', '-0.008446', '0.00732', '0.0002203', '-0.00759', '-0.006863', '0.002712', '-0.0002956', '-0.005783', '0.007465', '-0.004856', '0.001673', '0.006237', '-0.001728', '-0.00529', '-0.00556', '-0.007195', '0.00111', '-0.0003538', '-0.000509', '0.001982', '-0.0003848', '-0.003418', '0.002546', '-0.00462', '0.005535', '-0.005207', '0.00445', '-0.0063', '-0.00435', '0.008995', '0.000454', '-0.0002651', '0.003761', '0.00798', '0.00908', '-0.0003326', '-0.0002339', '0.004616', '-0.005325', '-0.002518', '-0.002241', '0.004185', '-0.00917', '0.000553', '-0.002337', '0.008026', '-0.005287', '-0.0004945', '-0.006382', '-0.001281', '0.003963', '-0.00795', '0.000571', '-0.00853', '0.004868', '-0.006702', '-0.01133', '-0.00896', '0.002495', '0.005238', '-0.005352', '0.00223', '-0.00915', '-0.00933', '0.001189', '-0.0006595', '-0.00828', '-0.005096', '9.096e-05', '-0.004158', '0.0006638', '-0.002506', '-5.466e-05', '0.000844', '0.001164', '0.002321', '-0.00659', '0.003803', '0.003202', '0.00929', '0.00985', '-0.002398', '0.008606', '0.002802', '-0.00435', '0.00776', '-0.003456', '0.004997', '0.00414', '0.0005755', '-0.00863', '-9.817e-05', '-0.00228', '0.010025', '0.004883', '0.001782', '0.001323', '-0.001327', '-0.00831']",,,,,,,
mondo:0014009,autosomal recessive congenital ichthyosis 7,"['autosomal recessive congenital ichthyosis type 7', 'ichthyosis, congenital, autosomal recessive 7', 'ARCI7']",0060716,615022,,C3554348,,,,,,,,
mondo:0014010,autosomal recessive congenital ichthyosis 9,"['autosomal recessive congenital ichthyosis type 9', 'ichthyosis, congenital, autosomal recessive 9', 'ichthyosis, congenital, autosomal recessive type 9', 'ARCI9']",0060718,615023,,C3554349,,,,,,,,
mondo:0014011,autosomal recessive congenital ichthyosis 10,"['ARCI10', 'autosomal recessive congenital ichthyosis type 10', 'ichthyosis, congenital, autosomal recessive 10', 'ichthyosis, congenital, autosomal recessive type 10']",0060719,615024,,C3554355,,,,,,,,
mondo:0014012,Charcot-Marie-Tooth disease axonal type 2Q,"['Charcot-Marie-Tooth neuropathy type 2Q', 'DHTKD1 Charcot-Marie-Tooth disease', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2Q', 'Charcot-Marie-Tooth disease, axonal, type 2Q', 'autosomal dominant Charcot-Marie-Tooth disease type 2Q', 'Charcot-Marie-Tooth disease type 2Q', 'Charcot-Marie-Tooth disease caused by mutation in DHTKD1', 'CMT2Q', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2Q', 'Charcot-Marie-Tooth neuropathy, type 2Q']",0110170,615025,329258,C3554366,"['0.1698', '0.173', '0.2974', '-0.1709', '0.02992', '-0.3748', '0.1969', '0.6123', '-0.7744', '-0.318', '0.1401', '0.3516', '-0.543', '0.305', '0.005856', '-0.196', '-0.2922', '-0.4126', '-0.66', '-0.577', '-0.01694', '0.4666', '0.37', '0.9155', '0.1982', '0.2065', '0.1704', '0.04758', '-0.08545', '-0.1597', '0.324', '-0.639', '0.0422', '0.12415', '0.481', '-0.7197', '-0.6636', '-0.1305', '0.293', '-0.0666', '-1.225', '-0.3804', '-0.3486', '0.3054', '-0.3218', '-0.3162', '0.0334', '-0.04852', '-0.05377', '0.04327', '0.259', '0.3013', '-0.3245', '-1.212', '-0.0832', '-0.183', '-0.4158', '0.2942', '-0.935', '-0.2155', '-0.3643', '-0.012596', '0.6167', '0.6797', '-1.035', '1.026', '-0.2167', '0.58', '-0.8164', '0.4749', '-0.7783', '-0.04047', '0.6245', '-0.3687', '1.286', '0.4028', '-0.1549', '0.662', '-0.05173', '-0.617', '-0.2361', '-0.1622', '0.8716', '0.539', '0.0087', '-0.0004642', '-0.01212', '0.618', '0.5537', '0.1443', '0.248', '-0.05328', '-0.0492', '0.5273', '0.4004', '0.61', '0.576', '-0.771', '-0.2976', '0.702']",,,,,,,
mondo:0014013,maternal riboflavin deficiency,"['RBFVD', 'riboflavin deficiency']",,,411712,,,,,,,,,
mondo:0014014,"epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive","['EBNS', 'EBS-AR exophilin 5', 'epidermolysis bullosa, nonspecific, autosomal recessive', 'epidermolysis bullosa simplex 4, localized or generalized intermediate, autosomal recessive', 'epidermolysis bullosa simplex due to exophilin 5 deficiency']",,615028,412189,C3554367,,,,,,,,
mondo:0014015,hereditary spastic paraplegia 56,"['hereditary spastic paraplegia caused by mutation in CYP2U1', 'autosomal recessive spastic paraplegia type 56', 'CYP2U1 hereditary spastic paraplegia', 'hereditary spastic paraplegia type 56', 'spastic paraplegia 56, autosomal recessive', 'SPG56', 'autosomal recessive spastic paraplegia 56']",0110808,615030,320411,C3539507,"['-0.1426', '0.04227', '0.001613', '-0.33', '-0.368', '-0.829', '-0.2554', '0.0198', '-0.5635', '-0.3599', '0.00911', '-0.1061', '0.1702', '0.2224', '0.9414', '0.127', '-0.1521', '-0.268', '0.06805', '-0.533', '0.2742', '0.115', '0.243', '0.3271', '0.04672', '0.07245', '0.0743', '0.1272', '-0.1473', '-0.342', '0.2318', '0.0948', '0.0395', '0.0872', '0.2009', '-0.4893', '-0.1886', '-0.5244', '-0.2778', '-0.2443', '0.03091', '-0.638', '-0.1914', '0.5337', '-0.0784', '-0.372', '-0.2744', '0.2947', '-0.1', '0.08356', '-0.2345', '0.145', '-0.4612', '-0.2377', '0.03937', '-0.68', '0.646', '-0.03378', '-0.2551', '0.4602', '-0.1948', '-0.08466', '0.2134', '0.358', '-0.5415', '0.2114', '-0.04315', '0.6396', '-0.2329', '0.491', '-0.3184', '-0.2079', '0.1757', '-0.381', '0.86', '0.2705', '-0.2976', '0.07947', '-0.139', '-0.1901', '-0.1057', '-0.3762', '0.6055', '0.932', '-0.04926', '0.04318', '-0.013466', '0.1936', '0.165', '0.163', '0.469', '-0.08563', '0.1343', '0.3262', '0.8623', '0.669', '0.5796', '-0.0916', '0.03934', '0.03778']",,,,,,,
mondo:0014016,hereditary spastic paraplegia 49,"['hereditary spastic paraplegia caused by mutation in TECPR2', 'neuropathy, hereditary sensory and autonomic, type IX, with developmental delay', 'autosomal recessive spastic paraplegia 49', 'autosomal recessive spastic paraplegia type 49', 'spastic paraplegia 49, autosomal recessive', 'TECPR2 hereditary spastic paraplegia', 'hereditary spastic paraplegia type 49', 'SPG49']",0110801,615031,320385,C3542549,"['-0.0741', '0.199', '0.258', '-0.5576', '-0.2595', '-0.4512', '-0.381', '0.2664', '-0.7407', '0.03906', '0.3665', '0.2031', '-0.1385', '-0.1476', '0.185', '0.0398', '0.3396', '0.02464', '-0.0633', '-0.3381', '0.358', '0.0597', '-0.324', '0.1627', '-0.03098', '0.1978', '0.2827', '-0.05972', '0.1057', '-0.414', '0.2202', '-0.04776', '0.3596', '-0.005116', '-0.1316', '-0.41', '-0.03864', '-0.189', '-0.1545', '-0.2014', '-0.2069', '-0.2712', '-0.06055', '0.1682', '-0.3333', '-0.4365', '0.226', '0.03586', '-0.1387', '0.00865', '-0.553', '0.42', '-0.1436', '-0.1136', '0.00704', '-0.2512', '0.274', '0.282', '0.1122', '0.1906', '-0.0737', '0.1971', '0.3184', '0.2688', '0.1853', '0.3823', '0.4321', '0.7085', '-0.4875', '0.3418', '-0.6426', '0.355', '0.3525', '-0.07306', '0.1111', '0.05325', '0.2394', '0.1114', '0.1819', '0.1599', '-0.064', '-0.06186', '0.1514', '0.4932', '-0.0665', '0.1045', '0.03323', '0.1642', '0.28', '0.2456', '0.1914', '0.1055', '0.3557', '0.08014', '0.577', '0.2471', '0.2537', '-0.05923', '0.2644', '0.2659']",,,,,,,
mondo:0014017,intellectual developmental disorder with autism and macrocephaly,"['AUTS18', 'autism, susceptibility to, 18', 'autism, susceptibility to, type 18', 'susceptibility to autism 18', 'CHD8 overgrowth syndrome']",,615032,642675,,,,,,,,,
mondo:0014018,hereditary spastic paraplegia 54,"['autosomal recessive spastic paraplegia 54', 'SPG54', 'DDHD2 autosomal recessive complex spastic paraplegia', 'hereditary spastic paraplegia type 54', 'autosomal recessive spastic paraplegia type 54', 'autosomal recessive complex spastic paraplegia caused by mutation in DDHD2', 'spastic paraplegia 54, autosomal recessive']",0110806,615033,320380,C4510083,"['-0.2007', '-0.06024', '0.05704', '-0.2937', '0.06714', '-0.878', '-0.3535', '0.177', '-0.7544', '-0.853', '-0.07434', '0.1688', '-0.265', '0.1532', '0.4346', '0.1451', '-0.04382', '-0.5273', '0.1805', '-0.2079', '0.3499', '-0.2094', '0.0008774', '0.0432', '0.1406', '0.139', '0.00756', '0.1104', '0.072', '-0.2365', '0.04218', '0.1737', '0.4197', '0.3264', '0.239', '-0.52', '-0.07764', '-0.2448', '-0.3188', '-0.36', '0.263', '-0.3494', '-0.02219', '0.566', '-0.1324', '-0.206', '0.0196', '0.5464', '0.249', '0.0741', '-0.09436', '-0.1324', '-0.6064', '-0.2386', '0.10583', '-0.857', '0.4482', '-0.1057', '-0.5786', '0.878', '-0.0953', '-0.05045', '0.4692', '0.504', '-0.4324', '-0.182', '0.1256', '0.71', '-0.342', '0.3315', '-0.2666', '0.02536', '0.3494', '-0.331', '0.8765', '0.4644', '-0.228', '0.03323', '-0.4365', '-0.04004', '0.223', '-0.261', '0.4402', '1.065', '-0.148', '0.05588', '0.2167', '0.1831', '0.2021', '0.155', '0.2323', '0.5938', '0.03632', '0.1519', '0.6357', '0.425', '0.677', '0.133', '0.2605', '-0.06134']",,,,,,,
mondo:0014019,dystonia 24,"['ANO3 dystonic disorder', 'dystonia 24', 'cranio-cervical dystonia with laryngeal and upper-limb involvement', 'dystonia type 24', 'DYT24', 'dystonic disorder caused by mutation in ANO3', 'DYT-ANO3']",0090052,615034,420485,C3554374,"['0.3352', '0.2722', '-0.1874', '-0.2825', '-0.1615', '-1.228', '0.625', '-0.1934', '-0.8003', '-0.1564', '1.07', '0.852', '-0.5005', '0.309', '0.519', '0.3643', '-0.02719', '-0.98', '-0.6665', '-1.062', '-0.10645', '0.223', '-0.2747', '-0.309', '-0.09766', '-0.003674', '-0.01312', '0.2358', '-0.00963', '0.009964', '0.334', '0.3098', '1.031', '-0.3916', '0.9863', '-0.1481', '0.1932', '-0.0847', '0.5845', '-0.5737', '0.4915', '-0.03403', '-0.336', '0.2216', '0.531', '-0.285', '-0.3154', '0.2356', '0.611', '0.06238', '-0.06274', '0.285', '0.4517', '0.07605', '0.456', '-0.206', '0.2668', '0.7686', '0.1798', '-0.2747', '-0.6357', '-0.4956', '0.1554', '-0.6597', '-1.177', '0.7593', '0.387', '0.4265', '-0.2377', '0.505', '-0.3684', '-0.2332', '0.2181', '-0.1384', '0.2544', '0.4988', '0.8247', '0.1628', '0.1003', '-0.3506', '-0.219', '0.1506', '0.475', '0.365', '0.934', '0.01475', '0.1747', '0.4639', '1.515', '0.277', '0.2998', '-0.1292', '0.354', '0.1615', '1.271', '-0.1614', '-0.588', '0.004963', '0.4475', '-0.4744']",,0009040,,,,,
mondo:0014020,hereditary spastic paraplegia 55,"['SPG55', 'autosomal recessive spastic paraplegia 55', 'autosomal recessive spastic paraplegia type 55', 'spastic paraplegia 55, autosomal recessive', 'hereditary spastic paraplegia type 55']",0110807,615035,320375,C4510214,"['-0.2778', '0.384', '0.0947', '-0.1215', '-0.001176', '-0.629', '-0.528', '0.2031', '-0.558', '-0.2988', '-0.02672', '0.103', '-0.04697', '-0.2966', '0.297', '-0.519', '0.1685', '-0.1051', '-0.012085', '-0.02565', '-0.1936', '-0.399', '-0.0702', '0.1654', '-0.12415', '0.2162', '0.1665', '0.02194', '-0.4478', '-0.356', '0.000528', '0.3723', '0.3', '-0.04764', '-0.284', '-0.5444', '-0.010254', '-0.1404', '-0.10974', '-0.4685', '0.2634', '-0.4646', '-0.12195', '0.348', '-0.1976', '-0.0704', '-0.1334', '0.0791', '0.3142', '0.09', '0.00646', '-0.0045', '-0.3357', '-0.06445', '0.2112', '-0.323', '0.625', '0.1164', '-0.3389', '0.3376', '0.02582', '0.3062', '0.611', '0.3435', '-0.1602', '0.3489', '0.4426', '0.4827', '-0.565', '0.07324', '-0.11926', '0.1299', '0.312', '-0.2043', '0.7573', '0.01306', '-0.0746', '0.3628', '0.02684', '0.02663', '0.04227', '-0.0213', '0.3145', '0.5703', '-0.3247', '0.164', '-0.1364', '0.3164', '0.1931', '-0.0881', '0.121', '0.2517', '0.2212', '-0.1126', '0.7124', '0.0898', '0.4287', '-0.1371', '-0.3406', '0.2004']",,,,,,,
mondo:0014021,familial episodic pain syndrome with predominantly upper body involvement,"['episodic pain syndrome, familial, 1', 'episodic pain syndrome, familial, type 1', 'FEPS1']",0111729,615040,391389,CN204968,"['-0.286', '-0.04794', '-0.2979', '-0.17', '-0.2039', '-0.507', '0.2527', '0.3914', '-0.3462', '0.0825', '-0.357', '0.224', '0.1349', '0.1487', '-0.3806', '0.2566', '0.02534', '-0.001221', '0.1348', '-0.31', '0.023', '-0.02216', '-0.014854', '-0.006912', '-0.1979', '0.1506', '0.1703', '0.02246', '-0.1661', '-0.0955', '0.00232', '0.1901', '0.05685', '0.00225', '-0.062', '-0.125', '-0.1575', '0.1862', '-0.09686', '-0.0643', '-0.1453', '-0.1873', '0.08264', '0.3616', '0.298', '0.11505', '-0.9946', '0.377', '0.2151', '0.614', '-0.721', '0.1852', '0.2937', '0.0803', '-0.05374', '-0.0958', '0.0803', '-0.3564', '-0.2893', '-0.1536', '0.1337', '0.347', '-0.2234', '-0.3237', '-0.1482', '0.0416', '0.3357', '0.361', '0.0901', '0.5186', '-0.269', '-0.018', '0.05707', '-0.02591', '0.05276', '0.548', '0.302', '0.277', '0.264', '-0.3723', '0.01682', '-0.1709', '0.2842', '-0.2534', '0.07996', '0.02216', '0.1565', '0.613', '0.3848', '0.2534', '0.2842', '-0.119', '0.2874', '0.264', '0.522', '0.2507', '0.4646', '-0.3635', '-0.2474', '0.2544']",,,,,,,
mondo:0014022,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10","['RXYLT1 muscular dystrophy-dystroglycanopathy, type A', 'MDDGA10', 'muscular dystrophy-dystroglycanopathy, type A caused by mutation in RXYLT1', 'Walker-Warburg syndrome or muscle-eye-brain disease, Tmem5-related', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 10', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 10']",0111239,615041,899,C3554381,,,,,,,,
mondo:0014023,congenital muscular dystrophy with intellectual disability and severe epilepsy,"['CDG-Iu', 'congenital disorder of glycosylation, type Iu', 'congenital disorder of glycosylation type Iu', 'congenital disorder of glycosylation type 1u', 'CMD with intellectual disability and severe epilepsy', 'CDG syndrome type Iu', 'DPM2-CDG', 'CDG Iu', 'CDG1U', 'carbohydrate deficient glycoprotein syndrome type Iu']",0080571,615042,329178,C3554385,"['0.1577', '-0.5127', '-0.4465', '-0.307', '0.733', '-0.9487', '0.2218', '0.3826', '-1.889', '-0.6772', '0.1273', '0.0447', '-0.04132', '0.456', '-0.2314', '0.2783', '-0.566', '-0.00476', '-0.453', '-0.6743', '0.2299', '0.076', '0.04855', '0.6865', '0.06', '-0.03873', '0.1407', '-0.871', '0.609', '-0.4211', '0.3687', '-0.1199', '0.572', '-0.001466', '0.11096', '0.06714', '-0.4353', '0.2085', '0.1375', '-0.4666', '0.1127', '-0.502', '-0.7256', '0.3022', '-0.7417', '0.2554', '0.4255', '0.7476', '-0.35', '0.523', '-0.1167', '-0.3086', '0.1367', '-0.7007', '0.09094', '-0.5127', '0.4133', '0.549', '0.0281', '0.0495', '0.1409', '0.01772', '-0.1578', '0.06433', '0.02771', '-0.111', '0.1017', '0.596', '-0.2015', '-0.02641', '-0.0827', '0.7705', '0.1874', '0.04572', '0.04285', '0.4958', '0.221', '-0.08563', '0.1274', '0.1614', '0.2278', '0.4998', '-0.3992', '0.03854', '0.1282', '-0.0551', '-0.5366', '-0.324', '0.826', '0.4182', '-0.1243', '0.3855', '0.2617', '0.667', '-0.515', '-0.00146', '0.5225', '-0.4414', '-0.1797', '0.2544']",,,,,,,
mondo:0014024,hereditary spastic paraplegia 43,"['autosomal recessive spastic paraplegia type 43', 'hereditary spastic paraplegia type 43', 'autosomal recessive complex spastic paraplegia caused by mutation in C19orf12', 'spastic paraplegia 43, autosomal recessive', 'C19orf12 autosomal recessive complex spastic paraplegia', 'autosomal recessive spastic paraplegia 43', 'SPG43']",0110795,615043,320370,C2680446,"['-0.1153', '0.08026', '0.0364', '-0.4792', '-0.0899', '-0.651', '-0.3533', '0.0609', '-0.4595', '-0.2847', '-0.2034', '-0.10187', '-0.3013', '0.3486', '0.5166', '0.1032', '-0.33', '-0.3196', '-0.1592', '-0.246', '0.2006', '-0.478', '0.1086', '0.4717', '0.0466', '0.1588', '0.2417', '-0.1738', '-0.1956', '-0.2062', '0.2817', '0.03354', '0.1489', '0.3965', '0.1504', '-0.4597', '-0.2957', '-0.386', '-0.1715', '-0.4834', '-0.01846', '-0.6914', '-0.1078', '0.3083', '0.0947', '-0.397', '-0.276', '0.3308', '-0.1979', '0.2184', '0.1807', '0.2656', '-0.219', '-0.2185', '0.06067', '-0.4817', '0.536', '-0.11676', '-0.3552', '0.2502', '-0.282', '-0.0407', '0.1478', '0.1954', '-0.774', '0.1037', '0.2482', '0.5674', '-0.1633', '0.6753', '-0.3708', '-0.05838', '-0.02531', '-0.575', '0.8467', '0.4', '-0.06793', '0.2231', '0.0353', '-0.259', '0.1587', '-0.3071', '0.63', '1.058', '0.007378', '0.02591', '0.2664', '0.1694', '0.01971', '-0.0763', '0.7207', '0.2212', '0.1678', '0.4175', '0.672', '0.5337', '0.521', '0.3308', '-0.03084', '0.151']",,,,,,,
mondo:0014025,lower motor neuron syndrome with late-adult onset,"['spinal muscular atrophy, Jokela type', 'SMAJ']",0081356,615048,276435,C3554398,"['-0.4065', '0.082', '-0.0654', '0.005615', '-0.1735', '-0.7334', '-0.23', '1.322', '-0.6274', '-0.2064', '0.0346', '0.303', '-0.3674', '0.2185', '0.447', '0.52', '-0.1923', '-0.1669', '-0.2051', '-0.435', '0.1082', '-0.1588', '0.3315', '0.2969', '-0.1147', '-0.269', '0.1458', '-0.08167', '-0.7046', '0.06775', '0.773', '0.1544', '-0.289', '-0.1661', '0.2961', '-0.3362', '-0.6377', '0.154', '0.12463', '-0.1239', '-0.399', '-0.3933', '-0.2659', '0.313', '0.0413', '0.0687', '-0.2411', '-0.0648', '-0.1593', '-0.0647', '-0.2708', '0.0745', '-0.3708', '-0.0658', '-0.1506', '-0.1996', '0.3875', '-0.67', '-0.03485', '-0.0616', '0.2407', '0.03278', '0.00953', '-0.151', '-0.8', '-0.0978', '0.602', '0.5854', '-0.2532', '-0.0933', '-0.2139', '-0.0784', '-0.01451', '0.01775', '0.8047', '0.3271', '0.0323', '-0.1705', '0.2195', '-0.1161', '0.3167', '-0.2588', '0.76', '0.46', '-0.2255', '0.643', '-0.2156', '0.004158', '0.4272', '-0.251', '0.5312', '-0.1102', '-0.06555', '0.1633', '0.488', '0.5264', '0.3936', '-0.2006', '-0.511', '0.05502']",,,,,,,
mondo:0014026,congenital stationary night blindness 1F,"['night blindness, congenital stationary, type 1F', 'CSNB1F', 'LRIT3 congenital stationary night blindness', 'night blindness, congenital stationary (complete), 1F, autosomal recessive', 'congenital stationary night blindness 1F autosomal recessive', 'congenital stationary night blindness caused by mutation in LRIT3', 'congenital stationary night blindness type 1F']",0110864,615058,,C3554399,,,,,,,,
mondo:0014027,hypotrichosis 11,"['hypt11', 'hypotrichosis 11', 'hypotrichosis type 11', 'HYPT11', 'hypotrichosis caused by mutation in SNRPE', 'SNRPE hypotrichosis']",0110708,615059,,C3554409,,,,,,,,
mondo:0014028,distal arthrogryposis type 5D,"['distal arthrogryposis caused by mutation in ECEL1', 'ECEL1 distal arthrogryposis', 'arthrogryposis, distal, type 5D', 'distal arthrogryposis type 5 without ophthalmoplegia', 'distal arthrogryposis type 5 without ophthalmoparesis', 'DA5D']",0111594,615065,329457,C3554415,"['-0.6167', '-0.05026', '-0.1467', '-0.222', '0.5225', '-0.7354', '-0.03113', '0.559', '-1.248', '-0.7334', '0.192', '0.1503', '-0.1494', '0.1167', '-0.11304', '0.5503', '0.6035', '-0.702', '-0.2664', '-0.3354', '0.004726', '0.08997', '0.2019', '0.0594', '0.1451', '0.35', '-0.3154', '0.001431', '0.2654', '-0.1332', '0.06067', '-0.1552', '0.348', '0.3682', '0.688', '-0.4763', '-0.2664', '-0.5283', '-0.1676', '-0.5107', '-0.3704', '-0.553', '0.1703', '0.3845', '0.3623', '0.04367', '-0.2942', '0.739', '0.1627', '0.073', '-0.415', '-0.0696', '-0.03467', '-0.2096', '-0.3516', '-0.5874', '0.1758', '-0.31', '0.05237', '-0.1326', '0.3083', '0.05695', '-0.1564', '0.1063', '0.001411', '0.0273', '0.3196', '0.2578', '-0.01315', '0.2532', '-0.516', '0.2101', '-0.03275', '-0.1874', '0.1998', '0.296', '0.005207', '0.09753', '-0.2935', '-0.1149', '0.4038', '-0.2096', '0.4736', '0.5234', '-0.2368', '0.2686', '-0.2556', '0.6694', '0.2317', '0.12164', '-0.0918', '-0.1736', '0.3926', '-0.1278', '0.6675', '-0.07886', '0.7363', '-0.503', '0.263', '0.2922']",,,,,,,
mondo:0014029,osteogenesis imperfecta type 14,"['OI14', 'osteogenesis imperfecta, type XIV', 'osteogenesis imperfecta caused by mutation in TMEM38B', 'osteogenesis imperfecta type XIV', 'osteogenesis imperfecta, type 14', 'OI, type 14', 'TMEM38B osteogenesis imperfecta']",0110343,615066,216820,C3554428,,,,,,,,
mondo:0014030,primary ciliary dyskinesia 20,"['ciliary dyskinesia, primary, 20, with or without situs inversus', 'ciliary dyskinesia, primary, type 20', 'primary ciliary dyskinesia 20 with or without situs inversus', 'CCDC114 primary ciliary dyskinesia', 'primary ciliary dyskinesia type 20', 'primary ciliary dyskinesia caused by mutation in CCDC114', 'CILD20', 'ciliary dyskinesia, primary, 20']",0110625,615067,,C3540844,,,,,,,,
mondo:0014031,"microcephalic primordial dwarfism, Alazami type","['Alazami syndrome', 'facial dysmorphism, intellectual disability, and primordial dwarfism', 'ALAZS']",,615071,319671,C3554439,"['-0.1356', '0.4355', '-0.2347', '0.001134', '0.5376', '0.01918', '0.4019', '1.123', '-0.98', '-0.769', '0.327', '-0.802', '0.5996', '0.4473', '-0.01184', '-0.2876', '0.08026', '-0.2312', '-0.4922', '-0.994', '-1.084', '0.0871', '0.8604', '0.0992', '-0.1605', '-0.6846', '-0.2776', '0.08124', '0.6426', '-0.2952', '0.1025', '-0.4128', '0.2014', '0.2028', '-0.2423', '-0.5703', '-0.1969', '0.06354', '0.286', '-0.323', '0.2708', '0.4863', '-0.6357', '-0.0744', '0.3054', '-0.1975', '0.0777', '0.16', '0.3752', '-0.206', '-0.4016', '-0.1833', '-0.4888', '0.403', '-0.1831', '-0.6943', '-0.597', '-0.2083', '0.7812', '0.1619', '-0.5684', '0.262', '-0.0471', '0.1744', '0.06143', '0.964', '-0.2278', '0.3252', '-0.3086', '0.222', '-0.2274', '0.17', '0.2313', '-0.497', '-0.10394', '0.384', '0.1869', '0.1305', '-0.5205', '0.09735', '-0.00535', '0.001878', '-0.02141', '-0.01466', '0.22', '0.02036', '0.2292', '0.3608', '0.554', '0.581', '-0.2034', '0.10315', '-0.5835', '-0.41', '0.594', '-0.2727', '0.2175', '-0.2198', '0.8765', '0.253']",,,,,,,
mondo:0014032,brachydactyly type A1C,"['BDA1C', 'brachydactyly type A1 caused by mutation in GDF5', 'GDF5 brachydactyly type A1', 'brachydactyly, type A1, C']",0110977,615072,,C3554446,,,,,,,,
mondo:0014033,dystonia 25,"['dystonia type 25', 'dystonia 25', 'autosomal dominant focal dystonia, DYT25 type', 'DYT25', 'dystonic disorder caused by mutation in GNAL', 'GNAL dystonic disorder']",0090055,615073,329466,C3554447,"['0.6006', '0.2117', '0.1302', '-0.3535', '-0.09955', '-1.081', '0.605', '-0.1256', '-0.6567', '-0.0484', '0.972', '0.9336', '-0.3445', '0.4158', '0.4114', '0.61', '0.1148', '-0.8438', '-0.7593', '-1.062', '-0.5435', '0.0746', '-0.1827', '-0.1667', '-0.4702', '0.02704', '-0.02177', '-0.0772', '0.06506', '0.05447', '0.2847', '0.4043', '1.229', '-0.2712', '0.5684', '0.01204', '0.548', '-0.0858', '0.5044', '-0.5913', '0.5063', '-0.1132', '-0.3052', '0.1274', '0.4631', '-0.295', '-0.4165', '0.0003963', '0.6406', '0.3882', '0.3008', '0.08685', '0.6323', '0.0089', '0.4482', '-0.1497', '-0.0932', '0.849', '-0.1392', '-0.3823', '-0.635', '-0.616', '-0.0485', '-0.6396', '-0.9844', '0.775', '0.4895', '0.176', '-0.3433', '0.641', '-0.2588', '-0.2952', '0.2695', '-0.314', '0.3645', '0.5537', '0.747', '0.1289', '-0.024', '-0.305', '-0.3718', '0.1296', '0.2627', '0.4233', '1.182', '-0.01749', '0.1326', '0.369', '1.631', '0.0296', '0.0544', '0.1348', '0.585', '0.3533', '1.085', '0.08923', '-0.673', '0.2479', '0.3455', '-0.2146']",,,,,,,
mondo:0014034,severe intellectual disability-poor language-strabismus-grimacing face-long fingers syndrome,"['GATAD2B-associated neurodevelopmental disorder', 'intellectual disability, autosomal dominant 18', 'intellectual disability, autosomal dominant type 18', 'autosomal dominant mental retardation 18', 'autosomal dominant non-syndromic intellectual disability 18', 'mental retardation, autosomal dominant type 18', 'MRD18', 'autosomal dominant intellectual disability 18', 'GAND syndrome', 'mental retardation, autosomal dominant 18']",0070048,615074,363686,C3554448,"['-0.2499', '-0.07263', '0.4116', '-0.2908', '0.1622', '-0.354', '0.0405', '0.5933', '-0.8545', '-0.3516', '0.01707', '-0.1226', '0.3823', '-0.2673', '0.07056', '0.2673', '0.4983', '-0.2451', '-0.00744', '-0.7563', '-0.05856', '0.2084', '0.1368', '0.02304', '0.4731', '-0.1693', '-0.2615', '0.1484', '0.3005', '-0.331', '0.2183', '0.0937', '0.241', '0.196', '0.08264', '-0.2323', '-0.1763', '-0.4246', '-0.0922', '-0.6953', '0.5073', '-0.2815', '-0.1329', '-0.108', '0.1028', '-0.5713', '0.1465', '0.3555', '0.09985', '-0.087', '-0.3152', '0.0902', '-0.1765', '0.06256', '-0.1274', '-0.6177', '-0.1821', '0.2081', '-0.05533', '0.05643', '-0.03647', '-0.041', '-0.1863', '0.3296', '0.04178', '0.00707', '0.1455', '0.0804', '-0.1545', '0.3296', '-0.552', '0.04346', '0.05072', '-0.187', '-0.02766', '0.2327', '0.3213', '-0.07227', '-0.2184', '0.03638', '-0.04697', '0.003653', '-0.1132', '0.4937', '0.1222', '0.139', '-0.4104', '0.4395', '0.1843', '0.53', '-0.2058', '0.428', '0.1857', '-0.02335', '0.758', '0.10254', '0.2194', '-0.383', '0.5522', '0.3079']",,,,,,,
mondo:0014035,severe intellectual disability-progressive spastic diplegia syndrome,"['autosomal dominant mental retardation 19', 'mental retardation, autosomal dominant 19', 'neurodevelopmental disorder with spastic diplegia and visual defects', 'autosomal dominant non-syndromic intellectual disability 19', 'MRD19', 'CTNNB1-related intellectual disability', 'intellectual disability, autosomal dominant type 19', 'intellectual disability, autosomal dominant 19', 'autosomal dominant intellectual disability 19', 'mental retardation, autosomal dominant type 19']",0070049,615075,404473,C3554449,"['-0.1864', '0.397', '0.1691', '-0.275', '-0.1919', '-0.7075', '-0.274', '0.3428', '-0.7744', '-0.378', '0.11414', '-0.3977', '0.2285', '0.0237', '0.3318', '-0.02452', '0.1584', '-0.0002902', '-0.2146', '-0.3472', '-0.06635', '-0.07684', '-0.2057', '-0.06134', '0.3044', '0.1394', '-0.05328', '-0.1086', '0.302', '-0.405', '0.1669', '0.0988', '0.1494', '-0.04282', '0.054', '-0.06537', '-0.368', '-0.3037', '-0.0708', '-0.2805', '0.6763', '-0.3145', '-0.6685', '-0.1606', '-0.03888', '-0.2822', '-0.1288', '0.3352', '0.0962', '-0.0793', '-0.1664', '0.2766', '-0.587', '-0.1044', '0.3604', '-0.2708', '-0.0879', '0.1606', '-0.11334', '0.144', '-0.0348', '0.434', '0.2072', '0.3818', '-0.1644', '0.2795', '0.02289', '0.2319', '-0.433', '0.3975', '-0.7183', '0.3218', '0.2957', '-0.1156', '0.0412', '0.4497', '0.2394', '-0.2688', '0.2089', '0.1307', '-0.01965', '-0.4263', '-0.171', '0.745', '0.2461', '0.2263', '-0.4194', '0.3577', '0.2705', '0.6255', '-0.2925', '0.2455', '0.1669', '0.12476', '0.7734', '-0.004635', '0.09973', '-0.08685', '0.5312', '0.1766']",,,,,G11.4,,
mondo:0014036,Alzheimer disease 17,"['Alzheimer^s disease 17', 'Alzheimer disease 17, late-onset', 'Alzheimer^s disease type 17', 'AD17', 'Alzheimer disease 17, late onset', 'Alzheimer disease 17']",0110049,615080,,C3554452,,,,,,,,
mondo:0014037,spermatogenic failure 11,"['SPGF11', 'azoospermia caused by mutation in KLHL10', 'KLHL10 azoospermia', 'spermatogenic failure type 11', 'spermatogenic failure 11']",0070180,615081,,C3554453,,,,,,,,
mondo:0014038,"colorectal cancer, susceptibility to, 12","['colorectal cancer, susceptibility to, 12', 'colorectal cancer caused by mutation in POLE', 'colorectal cancer, susceptibility to, type 12', 'POLE colorectal cancer', 'colorectal cancer, susceptibility to, on chromosome 12Q24', 'CRCS12', 'susceptibility to colorectal cancer 12']",,615083,,,,,,,,,,
mondo:0014039,mitochondrial DNA depletion syndrome 11,"['mtDNA maintenance syndrome due to MGME1 deficiency', 'PEO-myopathy-emaciation syndrome', 'mitochondrial DNA depletion syndrome type 11', 'mitochondrial DNA maintenance syndrome due to MGME1 deficiency', 'mitochondrial DNA depletion syndrome 11', 'MTDPS11', 'progressive external ophthalmoplegia-myopathy-emaciation syndrome', 'MGME1 mitochondrial DNA depletion syndrome', 'mitochondrial DNA depletion syndrome caused by mutation in MGME1']",0080129,615084,352447,C3554462,"['-0.715', '-0.08325', '0.4197', '-0.3093', '-0.2041', '-0.3967', '0.3184', '0.6797', '-0.4014', '0.1214', '-0.09894', '-0.1753', '-0.284', '-0.1658', '-0.154', '-0.01785', '-0.00897', '0.11273', '-0.3572', '-0.5977', '0.3313', '-0.2089', '-0.1915', '-0.0466', '0.1166', '-0.07385', '0.1616', '0.1633', '-0.06854', '-0.1658', '-0.0649', '0.1306', '0.5864', '-0.2142', '-0.048', '-0.536', '-0.3977', '-0.141', '-0.2856', '-0.09955', '-0.11475', '-0.4165', '-0.01938', '0.2761', '-0.196', '0.01179', '-0.0802', '0.2025', '-0.287', '0.00836', '-0.3801', '0.211', '0.06207', '-0.2935', '-0.1461', '-0.2751', '0.0646', '-0.1207', '-0.2568', '0.1797', '0.0998', '0.03104', '-0.1447', '-0.1904', '-0.648', '-0.010254', '0.3074', '0.5737', '-0.04944', '0.3699', '-0.2698', '0.1056', '0.2133', '-0.1918', '0.1833', '-0.03494', '0.3027', '0.001805', '-0.11816', '0.3123', '0.3406', '0.2473', '0.2515', '0.4', '-0.0795', '0.2296', '0.193', '0.2734', '0.3096', '-0.1542', '0.326', '0.327', '0.2218', '0.0632', '0.7266', '0.2433', '0.4917', '0.0956', '0.1833', '0.274']",,,,,,,
mondo:0014040,autosomal recessive osteopetrosis 8,"['autosomal recessive osteopetrosis type 8', 'SNX10 autosomal recessive malignant osteopetrosis', 'osteopetrosis, autosomal recessive type 8', 'SNX10 autosomal recessive osteopetrosis', 'OPTB8', 'osteopetrosis, autosomal recessive 8', 'autosomal recessive malignant osteopetrosis caused by mutation in SNX10']",0110940,615085,,C3554478,,C150556,,,,,,
mondo:0014041,"autism, susceptibility to, 19","['autism, susceptibility to, 19', 'AUTS19', 'susceptibility to autism 19', 'autism, susceptibility to, type 19']",,615091,,,,,,,,,,
mondo:0014042,left ventricular noncompaction 7,"['left ventricular noncompaction type 7', 'left ventricular noncompaction 7', 'LVNC7', 'left ventricular noncompaction caused by mutation in MIB1', 'MIB1 left ventricular noncompaction']",,615092,,C3554496,,C157266,,,,,,
mondo:0014043,microcephalic primordial dwarfism due to ZNF335 deficiency,"['microcephalic primordial dwarfism, Walsh type', 'microcephaly 10, primary, autosomal recessive', 'primary autosomal recessive microcephaly 10', 'MCPH10']",0070294,615095,329228,C4510378,"['-0.3018', '0.4182', '-0.3193', '-0.1877', '0.4407', '0.06122', '-0.2247', '1.281', '-1.024', '-0.518', '0.397', '-0.8896', '-0.1455', '-0.05954', '-0.06757', '-0.691', '0.3962', '0.007275', '-0.5923', '-1.315', '-1.373', '-0.08185', '0.7085', '0.03198', '-0.0733', '-0.4504', '-0.392', '-0.01932', '0.2454', '-0.2196', '-0.01814', '-0.555', '0.187', '-0.2856', '-0.5806', '-0.0706', '-0.1086', '0.1395', '0.4883', '-0.0778', '0.0488', '0.2898', '-0.592', '-0.1827', '0.506', '-0.2148', '-0.149', '0.1826', '0.556', '-0.2834', '-0.0419', '-0.0923', '-0.6216', '0.2358', '-0.3618', '-0.571', '-0.616', '-0.385', '0.5684', '0.2122', '-0.6357', '0.4167', '-0.094', '0.2751', '-0.1326', '1.241', '0.1656', '0.4565', '-0.2238', '0.1902', '-0.3777', '0.2212', '0.1993', '-1.202', '-0.4875', '0.1593', '-0.02078', '0.465', '-0.3926', '0.1476', '-0.4556', '0.0446', '-0.1079', '0.4102', '0.01529', '-0.3044', '0.006435', '0.1622', '0.595', '0.4102', '-0.06207', '0.0575', '-0.3545', '-0.788', '0.3657', '-0.616', '0.4731', '0.02972', '0.908', '0.2455']",,,,,,,
mondo:0014044,dysmorphism-conductive hearing loss-heart defect syndrome,['TYSHCHENKO syndrome'],,615102,289553,C3554774,,,,,,,,
mondo:0014045,Cowden syndrome 3,"['CWS3', 'SDHD Cowden disease', 'Cowden syndrome 3', 'Cowden disease caused by mutation in SDHD', 'Cowden syndrome type 3']",,615106,,C3554516,,,,,,,,
mondo:0014046,Cowden syndrome 4,"['CWS4', 'Cowden syndrome type 4', 'KLLN Cowden disease', 'Cowden disease caused by mutation in KLLN', 'Cowden syndrome 4']",0081000,615107,,C3554517,,,,,,,,
mondo:0014047,Cowden syndrome 5,"['CWS5', 'PIK3CA Cowden disease', 'Cowden disease caused by mutation in PIK3CA', 'Cowden syndrome type 5', 'Cowden syndrome 5']",0081001,615108,,C3554518,,,,,,,,
mondo:0014048,Cowden syndrome 6,"['Cowden syndrome 6', 'AKT1 Cowden disease', 'Cowden syndrome type 6', 'CWS6', 'Cowden disease caused by mutation in AKT1']",0081002,615109,,C3554519,,,,,,,,
mondo:0014049,urofacial syndrome 2,"['urofacial syndrome 2', 'LRIG2 Ochoa syndrome', 'Ochoa syndrome caused by mutation in LRIG2', 'UFS2', 'urofacial syndrome type 2']",,615112,,C3554520,,,,,,,,
mondo:0014050,isolated microphthalmia 8,"['isolated microphthalmia caused by mutation in ALDH1A3', 'MCOP8', 'microphthalmia, isolated type 8', 'microphthalmia, isolated 8', 'ALDH1A3 isolated microphthalmia', 'isolated microphthalmia type 8']",0060841,615113,,C3554524,,,,,,,,
mondo:0014051,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2","['mitochondrial complex IV deficiency, nuclear type 6', 'cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 2', 'fatal infantile encephalocardiomyopathy caused by mutation in COX15', 'COX15 fatal infantile encephalocardiomyopathy', 'CEMCOX2', 'cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 2']",0080358,615119,,C3554534,,,,,,,,
mondo:0014052,congenital myasthenic syndrome 8,"['myasthenic syndrome, congenital, with Pre- and postsynaptic defects', 'myasthenic syndrome, congenital, due to agrin deficiency', 'congenital myasthenic syndrome 8 with pre- and postsynaptic defects', 'myasthenic syndrome, congenital, type 8', 'myasthenic syndrome, congenital, 8, with pre- and postsynaptic defects', 'AGRN congenital myasthenic syndrome', 'CMS8', 'myasthenic syndrome, congenital, 8', 'congenital myasthenic syndrome caused by mutation in AGRN', 'congenital myasthenic syndrome type 8', 'congenital myasthenic syndrome due to agrin deficiency']",0110657,615120,,C3808739,,,,,,,,
mondo:0014054,lymphoproliferative syndrome 2,"['LPFS2', 'lymphoproliferative syndrome caused by mutation in CD27', 'lymphoproliferative syndrome type 2', 'CD27 lymphoproliferative syndrome', 'lymphoproliferative syndrome 2']",0060708,615122,,C3554540,,,,,,,,
mondo:0014055,"epilepsy, familial adult myoclonic, 4","['epilepsy, familial ADULT myoclonic, 4', 'cortical myoclonic tremor with epilepsy, familial, 4', 'FAME4', 'epilepsy, myoclonic, familial adult, 4']",0111693,615127,,C3554560,,,,,,,,
mondo:0014056,"melanoma, cutaneous malignant, susceptibility to, 9","['CMM9', 'susceptibility to cutaneous malignant melanoma 9', 'melanoma, cutaneous malignant, susceptibility to, type 9', 'melanoma, cutaneous malignant, 9', 'melanoma, cutaneous malignant, susceptibility to, 9']",,615134,,,,,,,,,,
mondo:0014057,"maple syrup urine disease, mild variant","['maple syrup urine disease, mild variant', 'MSUDMV']",,615135,,C3554575,,,,,,,,
mondo:0014058,facial dysmorphism-immunodeficiency-livedo-short stature syndrome,"['fils', 'fils syndrome', 'facial dysmorphism, immunodeficiency, livedo, and short stature']",,615139,352712,C3554576,"['-0.4958', '0.4673', '0.254', '-0.624', '-0.01733', '-0.08264', '0.3452', '0.4382', '-6.855e-05', '-0.226', '0.403', '0.1543', '0.131', '-0.04813', '-0.04745', '0.04242', '0.513', '0.1301', '-0.389', '-0.3376', '-0.1382', '-0.3552', '0.1997', '-0.1804', '0.3142', '-0.04944', '-0.3298', '-0.283', '-0.348', '-0.1492', '0.3838', '0.1876', '0.7114', '0.002539', '0.1128', '-0.08344', '-0.3533', '-0.2031', '-0.1466', '-0.4836', '-0.1021', '0.02748', '-0.0698', '-0.32', '-0.303', '-0.2365', '0.06464', '-0.104', '0.177', '-0.167', '-0.2028', '0.015465', '0.2274', '0.3413', '-0.3674', '0.0287', '-0.2744', '-0.578', '-0.1412', '0.3262', '-0.1075', '0.2097', '-0.4624', '0.0762', '0.1098', '-0.05', '0.2094', '0.4348', '-0.2252', '0.5703', '-0.2198', '0.1125', '0.07916', '0.04697', '-0.02625', '-0.3147', '0.2047', '-0.2131', '0.13', '0.03473', '-0.1445', '0.1049', '0.05978', '0.12354', '-0.2876', '-0.03128', '0.10767', '0.11774', '0.5674', '0.11957', '0.1539', '0.4795', '-0.1561', '-0.11444', '0.5312', '0.3762', '0.1825', '-0.331', '-0.02603', '0.4646']",,,,,,,
mondo:0014059,"microphthalmia, isolated, with coloboma 9","['microphthalmia, isolated, with coloboma caused by mutation in TENM3', 'microphthalmia, isolated, with coloboma type 9', 'TENM3 microphthalmia, isolated, with coloboma', 'MCOPCB9', 'microphthalmia, syndromic 15', 'microphthalmia, isolated, with coloboma 9']",,615145,,C3554592,,,,,,,,
mondo:0014060,progressive retinal dystrophy due to retinol transport defect,"['retinol dystrophy-iris coloboma-comedogenic acne syndrome', 'RDCCAS', 'retinal dystrophy, iris coloboma, and comedogenic acne syndrome']",,615147,352718,C3554593,"['-0.681', '-0.2247', '0.1953', '-0.3428', '0.1885', '-0.2742', '-0.3423', '0.273', '-0.0938', '0.06177', '-0.3564', '-0.362', '-0.2668', '-0.06076', '-0.12476', '-0.4414', '0.2625', '0.1041', '-0.445', '-0.5933', '-0.1912', '-0.2286', '0.10736', '0.3733', '-0.09985', '-0.05615', '-0.1448', '-0.2761', '-0.0895', '-0.02252', '0.2754', '0.05615', '0.2076', '0.3887', '-0.04202', '-0.03513', '-0.02077', '-0.0894', '-0.02597', '-0.3599', '0.2788', '-0.3274', '0.1211', '-0.1849', '-0.5576', '-0.01836', '0.3086', '-0.0549', '-0.10706', '0.2389', '0.2189', '0.2874', '0.3235', '-0.1978', '-0.03363', '-0.377', '0.4985', '-0.0697', '-0.508', '0.05356', '0.381', '-0.04916', '0.5', '0.04614', '0.2153', '-0.1277', '0.6436', '0.584', '-0.2961', '0.4368', '-0.3513', '-0.1807', '-0.01898', '-0.02579', '0.381', '-0.2117', '0.02226', '0.002062', '-0.1339', '0.1595', '0.346', '0.159', '0.0713', '0.582', '-0.02661', '-0.1692', '0.0351', '0.08484', '0.2227', '-0.002539', '0.2141', '0.456', '0.1307', '0.1304', '0.3125', '0.02841', '0.55', '-0.3618', '-0.2019', '0.4133']",,,,,H35.5,,
mondo:0014061,Steel syndrome,"['dislocated hips and radial heads, carpal coalition, scoliosis, and short stature', 'bilateral hip and radial head dislocations-short stature-scoliosis-carpal coalitions-pes cavus-facial dysmorphism syndrome', 'STLS', 'steel syndrome']",,615155,438117,C3554594,"['0.0008707', '0.003754', '0.003654', '0.001792', '-0.00399', '-0.01135', '-0.00919', '0.01507', '-0.0115', '0.004906', '-0.007362', '0.0001878', '0.00922', '0.011185', '8.25e-05', '2.82e-05', '-0.005146', '-0.01027', '-0.0006824', '-0.009895', '0.0008717', '-0.002195', '-0.0007', '0.004227', '0.0073', '0.003084', '-0.00575', '0.003223', '-0.004658', '-0.01112', '0.00783', '-0.01099', '0.005848', '-0.004776', '0.00395', '-0.004898', '0.00645', '0.00536', '-0.006336', '-0.00126', '-0.00105', '-0.01058', '0.011185', '-0.01136', '-0.00629', '-0.012665', '0.003834', '0.00516', '0.00639', '-0.00617', '-0.005894', '-0.007004', '0.007034', '0.0088', '-0.00736', '-0.010025', '2.58e-05', '0.003086', '-0.003094', '-0.00913', '0.013054', '0.00873', '0.001623', '-0.00632', '0.002016', '-0.001375', '0.001587', '0.01402', '-0.00471', '0.012276', '-0.01345', '0.000623', '-0.004997', '0.00343', '0.00877', '0.006374', '0.004864', '-0.001356', '-0.01416', '-0.009796', '-0.005924', '-0.005035', '-0.005093', '0.003374', '-0.012276', '-0.00211', '0.00778', '0.008064', '0.01877', '-0.006683', '0.00792', '0.006447', '0.006584', '0.00846', '0.00786', '-0.00335', '0.01185', '-0.011826', '0.002426', '0.00461']",,,,,,,
mondo:0014062,mitochondrial DNA deletion syndrome with progressive myopathy,"['PEOA6', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 6', 'mitochondrial DNA deletion syndrome with limb-girdle weakness', 'mtDNA deletion syndrome with limb-girdle weakness', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 6', 'progressive external ophthalmoplegia, autosomal dominant 6', 'mtDNA deletion syndrome with progressive myopathy']",0111519,615156,352470,C3554599,"['-0.8457', '0.1674', '0.0689', '-0.1835', '0.2057', '-0.5947', '0.06366', '0.368', '-0.575', '-0.05603', '0.1247', '-0.0381', '0.2128', '0.0009637', '0.1498', '-0.1373', '-0.0176', '0.03378', '-0.2705', '-0.5205', '0.087', '-0.1536', '0.1433', '0.0351', '0.10126', '0.02211', '-0.01854', '-0.1447', '-0.284', '-0.1256', '-0.07825', '0.2712', '0.505', '0.2343', '-0.02719', '-0.3486', '-0.2013', '-0.0898', '-0.02414', '-0.2257', '0.03864', '-0.288', '-0.3772', '0.4949', '-0.1971', '-0.2264', '-0.3032', '0.2311', '0.0896', '-0.005917', '-0.3723', '-0.1722', '0.07324', '-0.11255', '-0.122', '-0.3694', '0.417', '-0.3008', '-0.0785', '0.01791', '0.3152', '0.0461', '0.11847', '0.1595', '-0.5273', '0.0502', '0.494', '0.2969', '-0.2559', '0.166', '-0.2059', '-0.09863', '0.2256', '0.1871', '0.169', '-0.1444', '0.1242', '0.1375', '-0.2852', '0.1941', '0.275', '0.2546', '0.08887', '0.3035', '-0.1873', '0.1294', '0.04077', '0.4011', '0.1401', '-0.05972', '0.3909', '0.37', '0.252', '0.0765', '0.32', '0.2861', '0.5425', '-0.02098', '-0.0782', '0.201']",,,,,,,
mondo:0014063,mitochondrial complex III deficiency nuclear type 2,"['MC3DN2', 'mitochondrial complex III deficiency caused by mutation in TTC19', 'TTC19 mitochondrial complex III deficiency', 'mitochondrial complex III deficiency, nuclear type 2', 'mitochondrial Complex 3 deficiency, nuclear type 2']",0060351,615157,,C3554605,,,,,,,,
mondo:0014064,mitochondrial complex III deficiency nuclear type 3,"['mitochondrial complex III deficiency, nuclear type 3', 'mitochondrial Complex 3 deficiency, nuclear type 3', 'mitochondrial complex III deficiency caused by mutation in UQCRB', 'UQCRB mitochondrial complex III deficiency', 'MC3DN3']",0080112,615158,,C3554606,,,,,,,,
mondo:0014065,mitochondrial complex III deficiency nuclear type 4,"['MC3DN4', 'mitochondrial Complex 3 deficiency, nuclear type 4', 'mitochondrial complex III deficiency, nuclear type 4', 'mitochondrial complex III deficiency caused by mutation in UQCRQ', 'UQCRQ mitochondrial complex III deficiency']",0080113,615159,,C3554607,,,,,,,,
mondo:0014066,mitochondrial complex III deficiency nuclear type 5,"['mitochondrial complex III deficiency, nuclear type 5', 'UQCRC2 mitochondrial complex III deficiency', 'MC3DN5', 'mitochondrial complex III deficiency caused by mutation in UQCRC2', 'mitochondrial Complex 3 deficiency, nuclear type 5']",0080114,615160,,C3554608,,,,,,,,
mondo:0014067,short ulna-dysmorphism-hypotonia-intellectual disability syndrome,"['mental retardation, autosomal recessive 35', 'intellectual disability, autosomal recessive 35', 'MRT35']",0081201,615162,357175,C3554609,,,,,,,,
mondo:0014068,cone-rod dystrophy 17,"['CORD17', 'cone-rod dystrophy 17', 'cone-rod dystrophy type 17']",0111023,615163,,C3554610,,,,,,,,
mondo:0014069,syndactyly-camptodactyly and clinodactyly of fifth fingers-bifid toes syndrome,"['Wahab syndrome', 'Synactyly-camptodactyly and clinodactyly of fifth fingers-bifid halluces syndrome', 'WAHAB syndrome', 'camptodactyly, clinodactyly, syndactyly, and bifid toe syndrome']",,615170,357332,C3554611,,,,,,,,
mondo:0014070,oculocutaneous albinism type 7,"['oculocutaneous albinism type VII', 'OCA7', 'albinism, oculocutaneous, type VII', 'albinism, oculocutaneous, type 7', 'oculocutaneous albinism caused by mutation in LRMDA', 'LRMDA oculocutaneous albinism']",0070100,615179,352745,CN204524,"['0.2896', '0.1637', '-0.1832', '0.2795', '0.4688', '-0.07715', '-0.333', '0.2002', '-0.577', '-0.678', '0.537', '-0.2942', '0.05875', '0.936', '-0.2472', '0.2305', '0.581', '0.2015', '0.3096', '-0.518', '-1.128', '0.1247', '0.6772', '-0.4587', '-0.2415', '-0.06116', '-0.652', '0.1656', '0.5645', '0.096', '0.3962', '0.011635', '0.2255', '0.564', '-0.12366', '0.591', '-1.013', '-0.662', '-0.01539', '-0.4182', '1.386', '-0.2705', '-0.2852', '0.02371', '-0.4753', '-0.5396', '0.635', '-0.7695', '0.936', '0.5786', '-0.0968', '-0.582', '0.2394', '-0.2534', '0.6304', '0.2524', '0.0869', '0.8945', '-0.1211', '-0.652', '-0.1996', '-0.0008984', '0.4595', '0.0554', '-0.4639', '0.2778', '0.582', '0.5977', '-0.2185', '0.7646', '-0.0711', '0.487', '-0.11005', '-0.449', '0.7227', '0.08075', '-0.05417', '-0.2004', '0.165', '-0.1554', '0.736', '-0.5664', '0.457', '0.636', '-0.1913', '-1.611', '0.5576', '0.4465', '0.9424', '0.3887', '0.2732', '1.047', '-0.11395', '0.1085', '0.592', '0.4724', '-0.7437', '-0.208', '0.332', '0.3691']",,,,,,,
mondo:0014071,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11","['muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies, type A, 11', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 11', 'Walker-Warburg syndrome or muscle-eye-brain disease, B3Galnt2-related', 'B3GALNT2 muscular dystrophy-dystroglycanopathy, type A', 'MDDGA11', 'muscular dystrophy-dystroglycanopathy, type A caused by mutation in B3GALNT2', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 11']",0111230,615181,899,C3554638,,,,,,,,
mondo:0014072,"D,L-2-hydroxyglutaric aciduria","['combined D-2-hydroxyglutaric aciduria and L-2-hydroxyglutaric aciduria', 'D,L-2-HGA', 'D2L2AD', 'combined D-2-hydroxyglutaric acidemia and L-2-hydroxyglutaric acidemia', 'D,L-2-hydroxyglutaric acidemia', 'combined D-2- and L-2-hydroxyglutaric aciduria']",0111619,615182,356978,C4076194,"['-0.1935', '-0.1733', '-0.01846', '-0.267', '0.2017', '-0.07294', '-0.1031', '0.345', '-1.123', '0.2211', '-0.827', '-0.7417', '-0.272', '-0.2378', '-0.1242', '0.3486', '0.705', '0.1647', '-0.399', '-0.664', '0.306', '-0.1499', '0.663', '0.10956', '0.2205', '-0.3318', '0.1327', '-0.1702', '-0.3267', '-0.281', '0.3286', '0.0762', '0.522', '-0.0851', '0.0571', '-0.02837', '-0.603', '0.1117', '-0.0792', '-0.4346', '0.762', '-0.4736', '0.0748', '-0.2499', '-0.574', '-0.6255', '0.4102', '0.4226', '-0.04214', '0.576', '-0.10065', '-0.088', '-0.2318', '-0.2386', '-0.1203', '-0.0908', '-0.3086', '-0.1898', '-0.2478', '0.196', '0.00718', '-0.1133', '0.3943', '0.1292', '-0.506', '0.0317', '0.7134', '0.2903', '-0.68', '0.3145', '0.1067', '0.2866', '-0.2318', '0.2466', '-0.4905', '0.505', '1.042', '-0.5933', '-0.10034', '0.298', '0.593', '0.1609', '-0.10913', '0.516', '-0.1754', '0.2515', '-0.153', '0.3125', '0.2445', '0.587', '-0.00166', '0.4536', '0.04617', '0.04318', '0.3645', '0.6157', '0.1711', '0.01779', '0.0919', '0.649']",,,,270.8,,,
mondo:0014073,dilated cardiomyopathy 1II,"['cardiomyopathy, dilated, 1II', 'CRYAB familial isolated dilated cardiomyopathy', 'familial isolated dilated cardiomyopathy caused by mutation in CRYAB', 'CMD1II', 'dilated cardiomyopathy type 1II', 'cardiomyopathy, dilated, type 1II']",0110450,615184,,C3554649,,,,,,,,
mondo:0014074,Charcot-Marie-Tooth disease dominant intermediate F,"['GNB4-related intermediate Charcot-Marie-Tooth neuropathy', 'Charcot-Marie-Tooth disease dominant intermediate type F', 'Charcot-Marie-Tooth disease, dominant Intermediate type F', 'autosomal dominant intermediate Charcot-Marie-Tooth disease type F', 'DI-CMTF', 'CMTDIF', 'Charcot-Marie-Tooth disease, dominant intermediate F']",0110206,615185,352670,C3554654,"['0.1246', '0.3596', '0.2852', '-0.004257', '-0.0754', '-0.0858', '0.01913', '0.523', '-0.86', '0.0644', '0.0268', '0.3748', '-0.4233', '0.02553', '-0.05576', '-0.1743', '-0.1477', '-0.3394', '-0.45', '-0.7246', '0.2213', '0.2039', '0.4512', '0.769', '0.2532', '0.6177', '-0.09827', '0.0847', '0.08276', '-0.27', '0.1694', '-0.76', '0.2856', '0.2607', '0.03903', '-0.6978', '-0.5205', '-0.3252', '0.5366', '-0.4463', '-1.473', '-0.5537', '-0.525', '0.7056', '-0.2435', '-0.4204', '0.01018', '-0.1866', '0.086', '-0.1676', '0.02701', '0.2386', '-0.3643', '-0.838', '0.2896', '-0.3994', '-0.3396', '0.299', '-0.8203', '0.01692', '-0.5176', '-0.02766', '0.9053', '0.777', '-1.159', '0.9673', '0.04822', '0.8574', '-0.731', '0.5977', '-1.062', '0.2068', '0.4695', '-0.2854', '1.136', '0.4875', '-0.2842', '0.526', '0.2656', '-0.529', '-0.1194', '-0.1619', '0.9087', '0.6147', '0.0422', '0.02185', '0.0316', '0.909', '0.803', '0.2418', '0.1193', '-0.2822', '0.1816', '0.5', '0.4075', '0.5176', '0.5376', '-0.602', '-0.278', '0.613']",,,,,,,
mondo:0014075,cataract 39 multiple types,"['autosomal dominant cataract 39 multiple types', 'CRYGB early-onset non-syndromic cataract', 'early-onset non-syndromic cataract caused by mutation in CRYGB', 'CTRCT39', 'cataract 39, multiple types', 'cataract 39, multiple types, autosomal dominant']",0110236,615188,98995,C3808800,,,,,,,,
mondo:0014076,"dyskeratosis congenita, autosomal recessive 5","['autosomal recessive dyskeratosis congenita 5', 'dyskeratosis congenita, autosomal recessive 5', 'DKCB5', 'dyskeratosis congenita, autosomal recessive type 5', 'dyskeratosis congenita, autosomal dominant 4']",0070022,615190,3322,C3554656,"['-0.519', '0.1774', '0.03394', '-1.129', '0.5635', '-0.315', '0.1428', '0.303', '-0.3645', '-0.927', '-0.2212', '0.08844', '-0.4922', '-0.1414', '0.2073', '-0.3435', '0.443', '-0.04977', '-0.2764', '-1.23', '-0.1772', '-0.608', '0.2157', '-0.4949', '-0.4575', '-0.05426', '-0.5244', '-0.4595', '0.073', '-0.844', '0.569', '0.2019', '0.5093', '0.2266', '0.2346', '0.6074', '-0.5747', '-0.5283', '-0.2258', '0.1718', '-0.625', '0.02388', '0.555', '-0.1907', '-0.2854', '-0.735', '-0.0415', '0.03336', '-0.1971', '-0.529', '0.1415', '0.2878', '0.4094', '-0.08813', '-0.4397', '-0.1676', '-0.03897', '-0.0798', '-0.328', '0.2764', '0.11615', '0.1404', '0.3345', '-0.0652', '0.804', '-0.05362', '0.347', '0.4207', '-0.2776', '0.5005', '-0.4004', '-0.756', '-0.12213', '0.1844', '0.0662', '-0.265', '0.0793', '-0.567', '0.333', '-0.275', '-0.567', '0.211', '-0.553', '0.599', '-0.10175', '0.03638', '0.2751', '0.01715', '0.3235', '0.3848', '0.3455', '0.3252', '-0.2286', '-0.1862', '0.3708', '0.5986', '0.8267', '-0.14', '0.646', '0.2676']",C176928,,,,,,
mondo:0014077,cobblestone lissencephaly without muscular or ocular involvement,"['lissencephaly 5', 'lissencephaly type 2 without muscular or ocular involvement', 'LIS5', 'cobblestone lissencephaly without muscular or eye involvement', 'lissencephaly type 2 without muscular or eye involvement', 'lissencephaly type 5']",0112230,615191,352682,C3554657,"['-0.2272', '-0.06094', '0.0867', '-0.441', '0.2133', '-0.1976', '0.3142', '0.3767', '-0.617', '0.05933', '-0.3992', '-0.579', '-0.3662', '-0.1976', '0.3547', '-0.03516', '0.4087', '-0.8755', '-0.3167', '-0.5757', '0.1021', '0.069', '0.4631', '-0.1433', '0.12225', '-0.2004', '0.403', '-0.1473', '-0.0746', '0.2175', '0.1451', '-0.01564', '0.5596', '0.1268', '-0.0546', '0.2627', '-0.277', '0.2622', '-0.1908', '-0.5693', '0.2969', '-0.294', '-0.0342', '0.05273', '-0.04755', '-0.04257', '0.0695', '0.1481', '-0.2046', '-0.1261', '0.2937', '0.11084', '0.0763', '-0.2544', '-0.4119', '-0.076', '-0.12335', '-0.0653', '-0.5103', '0.028', '-0.1035', '-0.1138', '-0.0636', '-0.00907', '-0.4744', '0.3303', '0.3755', '0.241', '-0.512', '0.0727', '-0.432', '0.6885', '0.2905', '0.1687', '-0.0342', '-0.202', '0.4648', '-0.2424', '-0.2222', '-0.2856', '-0.1338', '0.2134', '-0.1417', '0.4556', '-0.247', '-0.0811', '0.1118', '0.6836', '0.4307', '0.1209', '-0.01599', '0.3562', '0.1693', '0.1199', '0.4175', '0.1583', '0.2166', '0.0763', '0.03906', '0.3975']",,,,,,,
mondo:0014078,platelet-type bleeding disorder 15,"['ACTN1 inherited bleeding disorder, platelet-type', 'macrothrombocytopenia, autosomal dominant, ACTN1-related', 'bleeding disorder, platelet-type, 15', 'inherited bleeding disorder, platelet-type caused by mutation in ACTN1', 'BDPLT15', 'autosomal dominant macrothrombocytopenia ACTN1-related']",0111053,615193,,C3554663,,,,,,,,
mondo:0014079,"restless legs syndrome, susceptibility to, 8","['RLS8', 'restless legs syndrome, susceptibility to, 8', 'restless legs syndrome 8']",,615197,,,,,,,,,,
mondo:0014080,osteosclerotic metaphyseal dysplasia,"['OSMD', 'osteosclerotic metaphyseal dysplasia']",0081111,615198,500548,C3554665,,,,,,,,
mondo:0014081,severe combined immunodeficiency due to CARD11 deficiency,"['immunodeficiency 11A', 'IMD11A', 'immunodeficiency type 11', 'CARD11 immunodeficiency', 'immunodeficiency 11', 'SCID due to CARD11 deficiency', 'IMD11']",0111957,615206,357237,C3554686,"['-0.548', '0.1984', '0.4707', '-0.184', '0.2174', '-0.1581', '0.237', '0.11395', '0.07635', '-0.1852', '-0.0266', '0.01941', '-0.1532', '-0.07886', '0.00438', '-0.12164', '0.1277', '0.12305', '-0.3044', '-0.3132', '-0.01463', '-0.2776', '0.5874', '-0.05746', '0.2134', '-0.1137', '0.02347', '-0.2421', '-0.406', '-0.29', '0.2646', '0.4675', '0.5996', '0.02147', '0.163', '-0.10785', '-0.4617', '0.05045', '-0.406', '-0.4758', '-0.2554', '-0.1893', '0.02449', '-0.1667', '-0.634', '-0.402', '-0.011345', '-0.195', '0.1239', '0.03592', '0.0965', '-0.303', '0.296', '-0.01445', '-0.289', '0.1376', '0.1252', '-0.4536', '-0.321', '0.1742', '-0.1852', '0.2554', '-0.10443', '0.1681', '0.3777', '-0.001878', '0.28', '0.1664', '-0.3296', '0.4663', '-0.1805', '-0.10077', '-0.11005', '-0.1627', '0.2019', '-0.1719', '0.0965', '0.1062', '0.138', '-0.04932', '-0.1744', '-0.1798', '0.0284', '0.12427', '-0.1595', '-0.1423', '0.33', '0.2133', '0.433', '-0.1946', '0.3965', '0.4014', '-0.1197', '0.09143', '0.6074', '0.754', '0.11426', '-0.683', '-0.05005', '0.1683']",,,,,,,
mondo:0014082,cryptosporidiosis-chronic cholangitis-liver disease syndrome,"['immunodeficiency 56', 'IMD56', 'IL21R immunodeficiency']",0111982,615207,357329,C3554687,"['-0.1342', '0.0311', '0.392', '-0.374', '0.3704', '0.00855', '0.04355', '-0.2854', '-0.1903', '0.771', '0.7856', '0.2031', '-0.10547', '0.3113', '-0.533', '-0.643', '0.03616', '0.06525', '-0.941', '-0.1421', '-0.731', '-0.05402', '0.202', '0.0948', '-0.0899', '-0.696', '-0.3962', '0.4216', '-0.3433', '-0.9004', '0.23', '0.4932', '0.5527', '-0.0242', '0.47', '-0.1136', '-1.588', '0.2605', '0.459', '-0.2335', '-0.2754', '-0.175', '-0.10504', '-0.524', '-0.1774', '-0.3457', '-0.0432', '-0.8364', '-0.089', '-0.1283', '-0.4106', '-0.3408', '0.379', '-0.03897', '-0.2976', '-0.268', '-0.2356', '0.4321', '-0.6553', '-0.3428', '0.218', '0.3428', '-0.06128', '0.1671', '0.133', '0.3809', '0.1755', '0.6187', '-0.2002', '0.04892', '-0.1837', '0.3105', '0.1279', '-0.832', '0.888', '0.2372', '0.7056', '0.2235', '0.1324', '0.6772', '-0.4966', '-0.3042', '-0.381', '-0.366', '0.3564', '0.1511', '0.3696', '-0.275', '0.543', '0.3086', '0.7344', '0.386', '-0.2566', '0.404', '0.7954', '0.06995', '-0.4307', '-0.693', '-0.5176', '-0.0338']",,,,,,,
mondo:0014083,"agammaglobulinemia 7, autosomal recessive","['agammaglobulinemia, autosomal recessive, due to PIK3R1 defect', 'AGM7', 'agammaglobulinemia 7, autosomal recessive', 'PIK3R1 autosomal agammaglobulinemia', 'autosomal agammaglobulinemia caused by mutation in PIK3R1']",0081139,615214,,C3554689,,,,,,,,
mondo:0014084,ataxia with oculomotor apraxia type 3,"['ataxia-oculomotor apraxia type 3', 'ataxia-oculomotor apraxia-3', 'AOA3', 'ataxia-oculomotor apraxia 3']",0060557,615217,,C3554690,,,,,,,,
mondo:0014085,"hydrocephalus, nonsyndromic, autosomal recessive 2","['congenital hydrocephalus caused by mutation in MPDZ', 'hydrocephalus, nonsyndromic, autosomal recessive 2', 'hydrocephalus, nonsyndromic, autosomal recessive type 2', 'MPDZ congenital hydrocephalus', 'hydrocephalus, congenital, 2, with or without brain or eye anomalies', 'HYC2']",,615219,,C3554691,,,,,,,,
mondo:0014086,osteogenesis imperfecta type 15,"['osteogenesis imperfecta, type 15', 'OI15', 'osteogenesis imperfecta, type XV', 'osteogenesis imperfecta caused by mutation in WNT1', 'osteogenesis imperfecta type XV', 'WNT1 osteogenesis imperfecta', 'OI, type 15']",0110347,615220,216820,C3808844,,,,,,,,
mondo:0014087,Smith-McCort dysplasia 2,"['SMITH-McCort dysplasia 2', 'Smith-McCort dysplasia 2', 'RAB33B Smith-McCort dysplasia', 'Smith-McCort dysplasia caused by mutation in RAB33B', 'Smith-McCort dysplasia type 2', 'Smc2']",0081271,615222,,C3714896,,,,,,,,
mondo:0014088,advanced sleep phase syndrome 2,"['advanced sleep phase syndrome caused by mutation in CSNK1D', 'FASPS2', 'advanced sleep-phase syndrome, familial, 2', 'familial advanced sleep phase syndrome 2', 'CSNK1D advanced sleep phase syndrome', 'advanced sleep phase syndrome, familial, type 2', 'advanced sleep phase syndrome type 2', 'advanced sleep phase syndrome, familial, 2']",0110012,615224,,C3808874,,,,,,,,
mondo:0014089,corneal intraepithelial dyskeratosis-palmoplantar hyperkeratosis-laryngeal dyskeratosis syndrome,"['CIDED', 'corneal intraepithelial dyskeratosis and ectodermal dysplasia', 'corneal intraepithelial dyskeratosis and ectodermal dysplasia, formerly', 'palmoplantar carcinoma, multiple self-healing', 'MSPC']",,616964,352662,CN204511,"['-0.37', '0.1631', '0.01009', '-0.2139', '0.004066', '-0.3833', '0.01588', '-0.1813', '-0.2795', '-0.03677', '-0.05057', '-0.00131', '-0.3408', '-0.2108', '-0.2515', '-0.2473', '0.4285', '-0.4648', '0.06287', '-0.7427', '-0.11285', '0.03577', '0.2576', '0.0734', '-0.02583', '0.3044', '-0.12494', '0.1282', '-0.00933', '-0.0951', '0.2461', '0.1256', '0.2588', '0.2795', '0.3179', '-0.1006', '-0.02888', '-0.1909', '0.02223', '-0.3396', '0.1555', '-0.3237', '0.03983', '-0.0693', '-0.0501', '-0.008896', '-0.2006', '0.1898', '-0.02469', '-0.0321', '0.04672', '0.2542', '0.3418', '0.02138', '-0.2427', '-0.0688', '0.4426', '-0.05283', '-0.4675', '-0.1921', '0.1735', '-0.11597', '-0.188', '-0.1357', '0.3086', '-0.1904', '0.447', '0.5103', '0.0629', '0.5303', '-0.608', '-0.281', '0.1876', '-0.00823', '-0.05048', '-0.1924', '0.0972', '-0.164', '0.03946', '-0.1931', '-0.0302', '0.01457', '-0.1965', '0.3552', '-0.01839', '-0.2246', '-0.225', '0.3567', '0.2917', '0.2147', '0.278', '0.0675', '0.1788', '0.296', '0.4087', '0.05472', '0.5327', '-0.2969', '0.2217', '0.1969']",,,,,,,
mondo:0014090,"polydactyly, postaxial, type A6","['polydactyly, postaxial, type A6', 'PAPA6']",,615226,,C3808889,,,,,,,,
mondo:0014091,mitochondrial complex V (ATP synthase) deficiency nuclear type 4,"['MC5DN4', 'mitochondrial Complex 5 (ATP synthase) deficiency, ATP5A1 type', 'mitochondrial complex V (ATP synthase) deficiency, nuclear type 4', 'mitochondrial complex deficiency caused by mutation in ATP5F1A', 'mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 4', 'ATP5F1A mitochondrial complex deficiency']",0060333,615228,,C3808899,,,,,,,,
mondo:0014092,schizophrenia 18,"['schizophrenia 18 with or without an affective disorder', 'chromosome 7q36.3 Duplication syndrome, 362-Kb', 'schizophrenia 18', 'schizophrenia susceptibility 18', 'schizoaffective disorder', 'SCZD18', 'schizophrenia type 18']",0070093,615232,,C3808913,,,,,,,,
mondo:0014093,retinitis pigmentosa 66,"['RBP3 retinitis pigmentosa', 'RP66', 'retinitis pigmentosa type 66', 'retinitis pigmentosa 66', 'retinitis pigmentosa caused by mutation in RBP3']",0110393,615233,,C3715216,,,,,,H35.5,,
mondo:0014094,severe congenital hypochromic anemia with ringed sideroblasts,"['severe congenital hypochromic sideroblastic anaemia', 'anemia, hypochromic microcytic, with iron overload 2', 'severe congenital hypochromic sideroblastic anemia', 'anemia, hypochromic microcytic, with iron overload type 2', 'AHMIO2']",,615234,300298,C4511137,"['-0.4133', '0.3127', '-0.2257', '0.4915', '0.771', '0.1666', '-0.4802', '0.4263', '-0.1904', '-0.537', '0.8027', '-0.1676', '0.3765', '0.481', '-1.191', '-0.00076', '-0.568', '0.3474', '-0.4485', '-0.69', '-0.3706', '-0.4277', '0.4243', '-0.2583', '0.8545', '-0.4119', '0.1554', '-0.4895', '0.6553', '0.1658', '0.157', '0.1355', '0.5005', '0.571', '0.3403', '-0.323', '-0.8735', '-0.667', '0.4202', '-0.326', '-0.6084', '0.08905', '0.0648', '-0.447', '-0.828', '-0.842', '0.3186', '0.3025', '0.2524', '-0.325', '0.563', '0.42', '1.019', '-0.08923', '0.4487', '-0.733', '0.2534', '0.3633', '-1.176', '0.1262', '-0.1329', '0.4204', '-0.2769', '-0.3848', '-0.1941', '0.3328', '0.04053', '0.8623', '-0.5415', '1.019', '0.9204', '-0.4558', '-0.4536', '-0.802', '0.1236', '1.155', '0.1687', '0.268', '0.344', '0.5254', '0.085', '-0.3416', '0.02545', '-0.002378', '0.616', '-0.4834', '-0.5376', '0.386', '0.781', '-0.1757', '0.8774', '0.3376', '-0.203', '0.1158', '0.6123', '0.9307', '0.1826', '-0.1436', '0.2664', '-0.718']",,,,,,,
mondo:0014095,dilated cardiomyopathy 1JJ,"['CMD1JJ', 'dilated cardiomyopathy type 1JJ', 'familial isolated dilated cardiomyopathy caused by mutation in LAMA4', 'cardiomyopathy, dilated, type 1Jj', 'cardiomyopathy, dilated, 1JJ', 'LAMA4 familial isolated dilated cardiomyopathy']",0110438,615235,,C3808935,,,,,,,,
mondo:0014096,microcephaly-intellectual disability-phalangeal and neurological anomalies syndrome,"['Woods-Crouchman-Huson syndrome', 'WOODS syndrome']",,615236,137658,C0796203,,,,,,,,
mondo:0014097,congenital short bowel syndrome,"['CSBS', 'congenital short bowel syndrome']",,,2301,,"['-0.5103', '0.00687', '-0.03098', '-0.10876', '-0.08374', '0.0999', '-0.01223', '0.3784', '-0.1814', '-0.11993', '0.2512', '-0.3213', '-0.2695', '0.3142', '-0.5864', '0.04254', '0.11865', '0.6855', '-0.3782', '-0.7363', '0.1156', '-0.183', '-0.0389', '-0.4304', '0.2593', '-0.2064', '0.1615', '0.3608', '0.759', '-0.263', '0.03384', '-0.1686', '0.0801', '0.2367', '0.0311', '-0.0564', '-0.02997', '0.0962', '0.12213', '0.772', '-0.2406', '-0.214', '0.03326', '-0.1313', '0.2517', '0.073', '-0.02827', '-0.1394', '0.7188', '-0.03867', '-0.3477', '-0.12134', '-0.0435', '-0.2433', '-0.5815', '-0.367', '-0.8467', '-0.0783', '-0.1635', '-0.2893', '0.586', '0.2534', '0.05347', '-0.1406', '-0.0154', '-0.0879', '0.1718', '0.468', '-0.3953', '0.676', '-0.2976', '0.312', '0.1444', '-0.5093', '0.2157', '0.4075', '0.00809', '0.463', '-0.1263', '0.10626', '-0.4097', '-0.5107', '0.0614', '0.3313', '-0.0779', '-0.11523', '0.2559', '0.002302', '0.157', '-0.666', '-0.1274', '0.05576', '-0.046', '0.1663', '0.748', '0.33', '0.05765', '-0.5566', '0.1178', '0.6855']",,,,,,,
mondo:0014098,CIDEC-related familial partial lipodystrophy,"['CIDEC-related FPLD', 'FPLD5', 'lipodystrophy, familial partial, associated with Cidec mutations', 'lipodystrophy, familial partial, type 5']",0070203,615238,435651,C3808940,,,,,,,,
mondo:0014099,"nephrotic syndrome, type 8","['NPHS8', 'nephrotic syndrome caused by mutation in ARHGDIA', 'nephrotic syndrome, type 8', 'ARHGDIA nephrotic syndrome']",0080389,615244,,C3808953,,,,,,,,
mondo:0014100,dilated cardiomyopathy 1KK,"['MYPN dilated cardiomyopathy', 'cardiomyopathy, hypertrophic, 22', 'CMD1KK', 'dilated cardiomyopathy caused by mutation in MYPN', 'dilated cardiomyopathy type 1KK', 'cardiomyopathy, familial hypertrophic, 22', 'cardiomyopathy, dilated, type 1Kk', 'cardiomyopathy, familial restrictive, 4', 'cardiomyopathy, dilated, 1KK']",0110445,615248,75249,,"['0.269', '-0.466', '-0.3674', '0.3367', '0.1095', '-0.08026', '0.583', '0.3828', '-0.1589', '-0.1809', '0.1342', '-0.3137', '-0.4546', '0.2722', '-0.4417', '0.2634', '-0.794', '-0.2439', '-0.03363', '-0.7646', '0.6885', '0.323', '1.066', '-0.003113', '0.3286', '-0.2227', '0.5635', '0.512', '-0.2822', '-0.0133', '0.875', '-0.03656', '0.9355', '0.41', '-0.0783', '-0.725', '-0.4077', '-0.3064', '0.957', '-0.5244', '0.2142', '0.603', '0.2351', '0.529', '0.3176', '0.87', '-0.258', '0.356', '0.1278', '-0.2314', '-0.2145', '0.1754', '0.5317', '-0.1776', '0.3328', '-0.4253', '-0.531', '0.275', '-0.553', '-0.2186', '-0.1236', '0.8037', '0.5054', '-1.153', '-0.746', '0.1411', '0.1562', '0.3918', '-0.449', '-0.0663', '-0.5464', '0.5244', '0.0832', '-0.1797', '-0.00963', '0.311', '-0.01114', '-0.1976', '-0.4714', '0.1929', '-0.01016', '-0.5195', '0.2078', '-0.3767', '0.694', '0.0002275', '0.5376', '-0.001565', '0.536', '-0.09534', '0.03674', '-0.2228', '-0.476', '0.1847', '0.8984', '0.532', '0.2279', '-0.515', '-0.4292', '-0.1422']",,,,,,,
mondo:0014101,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12","['muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 12', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type a, 12', 'Walker-Warburg syndrome or muscle-eye-brain disease, POMK-related', 'MDDGA12', 'POMK muscular dystrophy-dystroglycanopathy, type A', 'muscular dystrophy-dystroglycanopathy, type A caused by mutation in POMK']",0111235,615249,899,C3808964,,,,,,,,
mondo:0014102,hypogonadotropic hypogonadism 17 with or without anosmia,"['SPRY4 hypogonadotropic hypogonadism', 'HH17', 'hypogonadotropic hypogonadism 17 with or without anosmia', 'hypogonadotropic hypogonadism caused by mutation in SPRY4']",0090079,615266,,C3808971,,,,,,E23.0,,
mondo:0014103,hypogonadotropic hypogonadism 18 with or without anosmia,"['hypogonadotropic hypogonadism 18 with or without anosmia, Autosomal recessive, Autosomal dominant, Digenic dominant', 'hypogonadotropic hypogonadism 18 with or without anosmia', 'HH18', 'hypogonadotropic hypogonadism caused by mutation in IL17RD', 'IL17RD hypogonadotropic hypogonadism']",0090076,615267,,C3808975,,,,,,E23.0,,
mondo:0014104,"cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4","['cerebellar ataxia and mental retardation with or without quadrupedal locomotion 4', 'cerebellar ataxia, intellectual disability, and dysequilibrium syndrome type 4', 'dysequilibrium syndrome caused by mutation in ATP8A2', 'cerebellar ataxia and intellectual disability with or without quadrupedal locomotion 4', 'cerebellar ataxia, intellectual disability, and dysequilibrium syndrome 4', 'CAMRQ4', 'cerebellar ataxia, mental retardation, and dysequilibrium syndrome 4', 'ATP8A2 dysequilibrium syndrome', 'cerebellar ataxia, mental retardation, and dysequilibrium syndrome type 4']",,615268,,C3808977,,,,,,,,
mondo:0014105,hypogonadotropic hypogonadism 19 with or without anosmia,"['DUSP6 hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism caused by mutation in DUSP6', 'HH19', 'hypogonadotropic hypogonadism 19 with or without anosmia']",0090090,615269,,C3808981,,,,,,E23.0,,
mondo:0014106,hypogonadotropic hypogonadism 20 with or without anosmia,"['hypogonadotropic hypogonadism caused by mutation in FGF17', 'FGF17 hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism 20 with or without anosmia', 'HH20']",0090082,615270,,C3808983,,,,,,E23.0,,
mondo:0014107,hypogonadotropic hypogonadism 21 with or without anosmia,"['hypogonadotropic hypogonadism caused by mutation in FLRT3', 'FLRT3 hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism 21 with anosmia', 'HH21', 'hypogonadotropic hypogonadism 21 with or without anosmia']",0090093,615271,,C3808986,,,,,,E23.0,,
mondo:0014108,Fanconi anemia complementation group Q,"['ERCC4 Fanconi anaemia', 'Fanconi anemia caused by mutation in ERCC4', 'Fanconi anaemia caused by mutation in ERCC4', 'Fanconi anaemia complementation group type Q', 'Fanconi anemia, complementation group Q', 'Fanconi anemia complementation group type Q', 'Fanconi Anemia, complementation group type Q', 'ERCC4 Fanconi anemia', 'FANCQ']",0111093,615272,,C3808988,,,,,,,,
mondo:0014110,cataract 15 multiple types,"['cataract 15, multiple types', 'CTRCT15', 'early-onset non-syndromic cataract caused by mutation in MIP', 'MIP early-onset non-syndromic cataract']",0110251,615274,98995,C3809001,,,,,,,,
mondo:0014111,cataract 19 multiple types,"['cataract type 19', 'early-onset non-syndromic cataract caused by mutation in LIM2', 'CTRCT19', 'cataract 19, multiple types', 'cataract 19', 'LIM2 early-onset non-syndromic cataract']",0110263,615277,98984,C3809004,,,,,,,,
mondo:0014112,cardiofaciocutaneous syndrome 2,"['cardiofaciocutaneous syndrome type 2', 'kras cardiofaciocutaneous syndrome', 'cardiofaciocutaneous syndrome 2', 'CFC2', 'cardiofaciocutaneous syndrome caused by mutation in kras', 'KRAS cardiofaciocutaneous syndrome']",0111461,615278,,C3809005,,,,,,,,
mondo:0014113,cardiofaciocutaneous syndrome 3,"['CFC3', 'cardiofaciocutaneous syndrome 3', 'cardiofaciocutaneous syndrome caused by mutation in MAP2K1', 'cardiofaciocutaneous syndrome type 3', 'MAP2K1 cardiofaciocutaneous syndrome']",0111462,615279,,C3809006,,,,,,,,
mondo:0014114,cardiofaciocutaneous syndrome 4,"['cardiofaciocutaneous syndrome 4', 'MAP2K2 cardiofaciocutaneous syndrome', 'cardiofaciocutaneous syndrome type 4', 'CFC4', 'cardiofaciocutaneous syndrome caused by mutation in MAP2K2']",0111463,615280,,C3809007,,,,,,,,
mondo:0014115,hypomyelination with brain stem and spinal cord involvement and leg spasticity,"['hypomyelination with brainstem and spinal cord involvement and leg spasticity', 'aspartyl-tRNA synthetase deficiency', 'HBSL']",,615281,363412,C3809008,"['-0.197', '0.10913', '0.438', '-0.3867', '-0.1572', '-0.2125', '0.0809', '0.3398', '-0.6943', '-0.0501', '-0.539', '-0.2764', '-0.316', '-0.1923', '0.4414', '-0.1766', '-0.2451', '-0.465', '-0.03824', '-0.512', '0.1396', '-0.4377', '0.01605', '-0.2048', '0.0149', '-0.1404', '0.1483', '0.305', '-0.2886', '-0.04068', '-0.0929', '0.1713', '0.2094', '-0.157', '0.2634', '0.03693', '-0.12054', '-0.1814', '0.2449', '-0.4045', '-0.10504', '-0.281', '2.58e-05', '0.2961', '-0.2131', '-0.06616', '-0.08453', '0.1708', '-0.12244', '-0.2773', '0.1312', '0.2415', '-0.3726', '0.04593', '-0.3748', '-0.05807', '0.2024', '-0.03476', '-0.3684', '0.2346', '-0.08826', '0.1674', '-0.1816', '0.0973', '-0.6245', '0.2284', '0.402', '0.5254', '-0.1652', '0.3232', '-0.2229', '0.5146', '-0.1257', '-0.2091', '-0.1009', '0.1538', '0.3489', '0.07526', '-0.07983', '-0.258', '-0.374', '-0.08936', '0.3914', '0.918', '-0.2993', '-0.0583', '0.03757', '0.3909', '0.4229', '-0.1863', '0.4705', '0.4417', '0.00759', '0.0854', '0.75', '0.0727', '0.4392', '0.1511', '0.2426', '0.3708']",,,,,,,
mondo:0014116,complex cortical dysplasia with other brain malformations 2,"['KIF5C complex cortical dysplasia with other brain malformations', 'complex cortical dysplasia with other brain malformations type 2', 'cortical dysplasia, complex, with other brain malformations 2', 'complex cortical dysplasia with other brain malformations caused by mutation in KIF5C', 'cortical dysplasia, Complex, with Other brain malformations type 2', 'CDCBM2']",0090133,615282,,C3809013,,,,,,,,
mondo:0014117,Charcot-Marie-Tooth disease type 4B3,"['SBF1 Charcot-Marie-Tooth disease type 4', 'Charcot-Marie-Tooth disease with focally folded myelin', 'Charcot-Marie-Tooth disease, type 4B3', 'Charcot-Marie-Tooth disease type 4 caused by mutation in SBF1', 'CMT4B3']",0110194,615284,363981,C3695063,"['-0.05017', '0.1744', '-0.0554', '0.2542', '0.148', '-0.3057', '-0.08105', '0.7344', '-0.6846', '-0.05658', '-0.012276', '0.318', '-0.563', '0.1842', '-0.145', '-0.1501', '-0.253', '-0.593', '-0.5796', '-0.483', '0.4634', '0.4297', '0.2415', '0.77', '0.614', '0.539', '-0.05927', '0.5894', '0.0838', '-0.06586', '0.229', '-0.248', '0.07306', '0.1411', '0.5156', '-0.809', '-0.553', '-0.1803', '0.6846', '-0.2', '-1.4795', '-0.75', '-0.5947', '0.372', '-0.0394', '-0.0758', '-0.0296', '0.1263', '-0.0872', '-0.2678', '0.2164', '0.10284', '-0.578', '-1.042', '0.1552', '-0.1628', '0.05023', '0.2172', '-0.6265', '-0.1735', '-0.3462', '0.2698', '0.577', '0.6177', '-0.7974', '1.11', '0.05792', '0.4832', '-0.823', '0.2866', '-0.825', '0.383', '0.389', '-0.002087', '1.123', '0.3972', '-0.2905', '0.6294', '-0.0296', '-0.5', '0.0866', '-0.3704', '0.6865', '0.4639', '0.1759', '-0.1982', '0.3884', '1.004', '0.848', '0.593', '0.5444', '-0.2522', '-0.01323', '0.2515', '0.525', '0.338', '0.6274', '-0.645', '0.06018', '0.375']",,,,,,,
mondo:0014118,congenital neutropenia-myelofibrosis-nephromegaly syndrome,"['SCN5', 'congenital neutropenia-bone marrow fibrosis-nephromegaly syndrome', 'vps45 deficiency', 'neutropenia, severe congenital, 5, autosomal recessive']",0112132,615285,369852,C3809031,"['-0.4553', '0.1713', '0.1315', '-0.438', '0.03207', '0.4558', '-0.1931', '0.957', '-0.5576', '-0.7705', '0.05176', '-0.1409', '-0.1898', '-0.1213', '-0.1228', '-0.153', '-0.806', '0.169', '0.4539', '-0.527', '0.07513', '-0.4412', '0.1488', '-0.336', '0.2264', '-0.006615', '0.1665', '0.05524', '-0.385', '0.435', '-0.0012', '-0.4617', '0.5664', '0.0704', '0.4595', '0.1854', '-0.8643', '-0.2017', '0.53', '-0.684', '0.07996', '0.33', '0.0656', '0.248', '0.01292', '-0.3916', '-0.4197', '-0.1571', '0.3281', '-0.4849', '0.1835', '0.1665', '0.5713', '0.2576', '-0.01047', '0.3389', '-0.5625', '-0.0655', '-0.3284', '0.03336', '-0.0806', '0.1582', '0.1328', '-0.2751', '-0.3086', '0.0836', '0.1366', '0.0826', '-0.3447', '0.7803', '-0.2705', '0.3057', '0.088', '-0.3484', '0.0486', '0.02313', '0.004494', '0.4602', '1.146', '0.0966', '-0.2075', '-0.116', '0.0656', '-0.1954', '-0.3022', '-0.11926', '0.5063', '0.654', '0.5205', '-0.2395', '-0.2062', '0.03452', '-0.878', '-0.3513', '0.742', '0.77', '-0.1108', '-0.526', '0.3264', '0.1919']",,,,,,,
mondo:0014119,intellectual disability-strabismus syndrome,"['mental retardation, autosomal recessive type 36', 'MRT36', 'mental retardation, autosomal recessive 36', 'neurodevelopmental disorder with brain abnormalities, poor growth, and dysmorphic facies', 'intellectual disability, autosomal recessive type 36', 'intellectual disability, autosomal recessive 36']",0081099,615286,363528,C3809039,"['-0.284', '0.0978', '0.6445', '-0.6187', '0.0841', '-0.2722', '0.144', '0.509', '-0.3538', '-0.1552', '-0.2411', '-0.3875', '-0.0323', '-0.3518', '-0.1671', '-0.2593', '0.1775', '-0.08234', '-0.4578', '-0.6274', '0.1522', '0.02385', '-0.01061', '-0.1998', '0.1587', '-0.1276', '0.02376', '-0.0619', '0.0791', '-0.3586', '0.1135', '-0.002998', '0.732', '0.07666', '0.001569', '0.04037', '-0.2847', '-0.295', '-0.11957', '-0.279', '0.335', '-0.05902', '-0.2152', '0.02618', '-0.03247', '-0.3853', '0.1748', '0.0907', '-0.1316', '0.09265', '-0.02817', '0.3674', '-0.1528', '-0.2051', '-0.1637', '0.2424', '-0.0634', '-0.10876', '-0.3047', '0.396', '0.03375', '0.0735', '-0.10443', '0.03574', '-0.3367', '-0.0039', '0.2385', '0.291', '-0.376', '0.1976', '-0.255', '0.51', '-0.02264', '-0.3027', '-0.1917', '-0.06635', '0.4631', '-0.2472', '-0.3013', '0.01137', '0.1488', '0.12335', '-0.0532', '0.439', '0.002926', '0.1282', '-0.04266', '0.2864', '0.341', '0.265', '0.0672', '0.4182', '-0.02339', '0.1062', '0.4192', '0.2676', '0.3735', '0.0111', '0.564', '0.4116']",,,,,,,
mondo:0014120,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A13","['MDDGA13', 'Walker-Warburg syndrome or muscle-eye-brain disease, B3Gnt1-related', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 13']",0111238,615287,899,C3809042,,,,,,,,
mondo:0014121,autosomal dominant childhood-onset proximal spinal muscular atrophy with contractures,"['Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy with contractures', 'spinal muscular atrophy, lower extremity-predominant 2, autosomal dominant', 'SMALED2', 'autosomal dominant spinal muscular atrophy, lower extremity-predominant 2', 'spinal muscular atrophy, lower extremity-predominant, 2A, autosomal dominant', 'spinal muscular atrophy, LOWER extremity-predominant, 2, autosomal dominant']",0070349,615290,363454,C3809049,"['-0.1177', '0.11316', '0.11096', '-0.1368', '0.06235', '-0.3118', '0.01736', '0.281', '-0.306', '-0.11383', '-0.0833', '-0.02217', '-0.1245', '0.01407', '0.1172', '-0.0525', '0.0337', '-0.0769', '-0.0704', '-0.3552', '-0.04053', '-0.1044', '0.07336', '-0.01171', '0.02533', '0.01813', '-0.01087', '-0.0798', '-0.1049', '-0.167', '0.04993', '0.04663', '0.1558', '0.0173', '-0.0216', '-0.0822', '-0.006447', '-0.04004', '0.08264', '-0.2101', '-0.04572', '-0.266', '-0.05606', '0.06052', '-0.0993', '-0.1274', '-0.074', '0.1996', '-0.0006', '0.0285', '-0.00743', '0.00389', '0.08984', '-0.1008', '-0.07086', '-0.1868', '0.1696', '0.001216', '-0.1442', '0.01435', '0.0938', '-0.005783', '-0.05823', '-0.02232', '-0.1177', '-0.002441', '0.1904', '0.2236', '-0.1105', '0.03708', '-0.2202', '0.0033', '0.04333', '-0.1626', '0.1647', '0.07623', '0.0369', '0.023', '-0.0749', '-0.026', '0.02795', '0.05728', '0.0515', '0.289', '-0.07135', '0.1362', '0.0913', '0.1967', '0.1401', '0.003119', '0.1175', '0.1593', '0.0643', '0.09485', '0.3218', '0.0967', '0.346', '-0.09735', '0.01146', '0.10504']",,,,,,,
mondo:0014122,"myofibromatosis, infantile, 2","['myofibromatosis caused by mutation in NOTCH3', 'myofibromatosis, infantile, 2', 'NOTCH3 myofibromatosis', 'myofibromatosis, infantile, type 2', 'myofibromatosis, infantile 2', 'IMF2']",,615293,,C3809084,,,,,,,,
mondo:0014123,primary ciliary dyskinesia 21,"['DRC1 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, type 21', 'ciliary dyskinesia, primary, 21', 'CILD21', 'primary ciliary dyskinesia 21 without situs inversus', 'ciliary dyskinesia, primary, 21, without situs inversus', 'primary ciliary dyskinesia type 21', 'primary ciliary dyskinesia caused by mutation in DRC1']",0110596,615294,,C3809087,,,,,,,,
mondo:0014124,Adams-Oliver syndrome 4,"['Adams-Oliver syndrome 4', 'AOS4', 'Adams-Oliver syndrome type 4', 'Adams-Oliver syndrome caused by mutation in EOGT', 'EOGT Adams-Oliver syndrome']",,615297,,C3809092,,,,,,,,
mondo:0014125,"symphalangism, proximal, 1B","['symphalangism, proximal, 1B', 'symphalangism, proximal, type 1B', 'SYM1B', 'GDF5 proximal symphalangism (disease)']",0080788,615298,,C3809104,,,,,,,,
mondo:0014126,Perrault syndrome 4,"['Perrault syndrome caused by mutation in LARS2', 'LARS2 Perrault syndrome', 'Perrault syndrome 4', 'PRLTS4', 'Perrault syndrome type 4']",,615300,,C3809105,,,,,,,,
mondo:0014127,oculocutaneous albinism type 5,"['OCA5', 'oculocutaneous albinism type V', 'albinism, oculocutaneous, type V']",0070099,615312,370091,CN204842,,,,,,,,
mondo:0014128,TCF12-related craniosynostosis,"['craniosynostosis type 3', 'TCF12 craniosynostosis', 'craniosynostosis 3', 'CRS3', 'craniosynostosis caused by mutation in TCF12']",,615314,,C3715051,,,,,,,,
mondo:0014130,Dowling-Degos disease 2,"['POFUT1 Dowling-Degos disease', 'Dowling-Degos disease caused by mutation in POFUT1', 'Dowling-Degos disease 2', 'Dowling-Degos disease type 2', 'DDD2']",,615327,,C3809147,,,,,,,,
mondo:0014131,hypohidrosis-enamel hypoplasia-palmoplantar keratoderma-intellectual disability syndrome,"['SHNS', 'SHAHEEN syndrome']",,615328,363523,C3809160,"['-0.5', '-0.1698', '0.02684', '-0.2698', '0.04916', '-0.2546', '0.249', '0.4585', '-0.3142', '-0.1573', '-0.04156', '-0.1859', '0.06415', '-0.5015', '0.10565', '0.1208', '0.557', '-0.491', '-0.3464', '-0.8687', '0.09753', '0.02306', '0.1786', '0.1405', '0.7715', '-0.1054', '-0.441', '0.1454', '0.0987', '-0.3562', '0.3752', '-0.1526', '-0.05283', '0.196', '0.1721', '0.00843', '-0.415', '-0.0931', '-0.05255', '-0.6953', '0.1687', '-0.0811', '-0.339', '-0.3052', '-0.1398', '-0.4248', '0.01344', '0.1449', '0.1265', '-0.1283', '-0.5176', '0.0385', '-0.2195', '0.502', '-0.3347', '0.1699', '0.132', '-0.3918', '0.0708', '0.10065', '0.049', '0.2023', '-0.05676', '0.08325', '-0.00628', '0.2291', '0.0717', '0.4668', '-0.0486', '0.2576', '-0.778', '-0.03137', '0.01752', '-0.109', '-0.443', '-0.05457', '0.4165', '-0.3103', '-0.113', '0.2474', '0.0989', '-0.1147', '-0.0817', '0.627', '-0.05438', '-0.006233', '-0.3606', '0.4128', '0.518', '0.655', '-0.177', '0.3057', '0.3213', '0.276', '0.7144', '0.00251', '0.0576', '-0.477', '0.547', '0.3167']",,,,,,,
mondo:0014132,multiple mitochondrial dysfunctions syndrome 3,"['fatal multiple mitochondrial dysfunctions syndrome caused by mutation in IBA57', 'multiple mitochondrial dysfunctions syndrome 3', 'IBA57 fatal multiple mitochondrial dysfunctions syndrome', 'IBA57 deficiency', 'multiple mitochondrial dysfunctions syndrome type 3', 'MMDS3']",0080135,615330,363424,C3809165,"['-0.4917', '0.2391', '-0.10144', '0.11755', '-0.04782', '-0.422', '-0.1261', '0.1226', '-0.6694', '0.04425', '-0.3215', '-0.2732', '-0.08307', '0.000821', '0.419', '-0.3115', '-0.1362', '-0.3074', '-0.179', '-0.505', '0.1943', '-0.269', '0.3464', '-0.4175', '0.2177', '-0.1169', '-0.02737', '0.3396', '-0.2947', '0.1205', '0.2583', '0.1466', '0.4478', '0.3113', '-0.0752', '0.06366', '-0.1559', '-0.1852', '-0.1771', '0.1364', '0.2076', '-0.1522', '0.03806', '-0.0799', '-0.198', '-0.184', '-0.1096', '-0.2185', '-0.01982', '-0.002964', '0.1167', '0.3188', '-0.2644', '-0.2068', '-0.004684', '-0.1587', '0.301', '0.089', '0.2542', '0.362', '-0.05576', '0.02037', '0.2357', '-0.4546', '-0.1926', '0.2693', '0.4944', '0.548', '-0.3806', '0.3884', '-0.0525', '0.385', '-0.2042', '-0.03616', '0.01158', '-0.1426', '0.523', '-0.12366', '0.03677', '-0.06165', '-0.07825', '-0.3042', '-0.0804', '0.591', '0.0188', '0.1364', '0.2827', '0.509', '0.4568', '0.2852', '0.5264', '0.21', '-0.2428', '0.03995', '0.2893', '0.377', '0.3584', '-0.1777', '0.3489', '-0.07117']",,,,,,,
mondo:0014133,"developmental and epileptic encephalopathy, 16","['epileptic encephalopathy, early infantile, type 16', 'developmental and epileptic encephalopathy 16', 'DEE16', 'EIEE16', 'epileptic encephalopathy, early infantile, 16']",0080449,615338,352596,C3809173,"['1.117', '0.2433', '-0.4502', '-0.1747', '-0.4417', '-0.6016', '0.8926', '0.4863', '-0.757', '-0.3208', '0.03497', '-0.299', '-0.4468', '0.428', '-0.2627', '0.0513', '-0.1868', '-0.559', '-0.4634', '-0.4944', '-0.2164', '0.5996', '0.0158', '-0.7007', '-0.292', '-0.05383', '0.05258', '-0.1241', '-0.528', '0.4087', '0.25', '-0.675', '0.3652', '0.3604', '0.6426', '0.4705', '-0.03836', '0.0849', '-0.1893', '-0.11005', '-0.01897', '-0.5103', '-0.1466', '-0.1195', '-0.4968', '-0.6597', '-0.4429', '-0.003674', '0.2299', '0.559', '-0.1688', '0.082', '0.2169', '-0.6255', '-0.02223', '-0.3284', '-0.2744', '0.0726', '-0.09314', '0.1663', '-0.9546', '0.459', '0.841', '-0.3264', '-0.4778', '1.385', '0.3682', '0.11224', '-0.77', '0.6484', '0.849', '0.8657', '0.1041', '-0.3994', '-0.02159', '0.675', '1.061', '0.3171', '-0.443', '0.3044', '-0.1517', '0.8584', '0.372', '0.07806', '0.2527', '0.3577', '0.06058', '0.599', '0.787', '0.3342', '0.1433', '0.1886', '-0.146', '0.177', '0.00994', '0.1749', '0.4275', '-0.4075', '0.5', '0.2107']",,,,,,,
mondo:0014134,"pulmonary hypertension, primary, 2","['SMAD9 primary pulmonary hypertension', 'primary pulmonary hypertension caused by mutation in SMAD9', 'PPH2', 'pulmonary hypertension, primary, type 2', 'pulmonary hypertension, primary, 2']",,615342,,C3888002,,,,,,,,
mondo:0014135,"pulmonary hypertension, primary, 3","['primary pulmonary hypertension caused by mutation in CAV1', 'pulmonary hypertension, primary, type 3', 'CAV1 primary pulmonary hypertension', 'pulmonary hypertension, primary, 3', 'PPH3']",,615343,,C3809192,,,,,,,,
mondo:0014136,"pulmonary hypertension, primary, 4","['primary pulmonary hypertension caused by mutation in KCNK3', 'PPH4', 'KCNK3 primary pulmonary hypertension', 'pulmonary hypertension, primary, 4', 'pulmonary hypertension, primary, type 4']",,615344,,C3809198,,,,,,,,
mondo:0014137,"precocious puberty, central, 2","['precocious puberty, central, type 2', 'central precocious puberty caused by mutation in MKRN3', 'CPPB2', 'precocious puberty, central, 2', 'MKRN3 central precocious puberty']",0112309,615346,,C3809199,"['-0.02802', '0.02782', '0.004673', '-0.01181', '0.02042', '-0.02963', '-0.005917', '0.04358', '-0.02591', '-0.02303', '-0.02156', '0.005207', '-0.005436', '0.00898', '0.001067', '-0.01471', '-0.006397', '-0.01301', '-0.01333', '-0.05463', '8e-07', '-0.004566', '0.02664', '-0.01332', '0.01053', '0.005486', '-0.0001432', '-0.005566', '-0.002253', '-0.02892', '0.02309', '0.003725', '0.04245', '0.01572', '0.01125', '-0.001864', '-0.002806', '-0.01464', '-0.00965', '-0.02579', '0.02426', '-0.013794', '0.009315', '0.0052', '-0.001193', '-0.02975', '-0.011795', '0.0168', '-0.00909', '0.01545', '0.001026', '-0.01061', '0.01055', '0.00424', '-0.01968', '-0.001251', '0.02205', '-0.01055', '-0.02669', '0.01305', '0.02094', '0.00855', '-0.00945', '0.003733', '-0.01007', '0.002079', '0.0285', '0.03207', '-0.0284', '0.02388', '-0.0292', '-0.004314', '0.00505', '-0.02733', '0.0177', '0.002577', '0.002317', '0.000812', '-0.01994', '-0.02959', '0.002373', '-0.0009174', '0.0035', '0.010864', '-0.01115', '0.001672', '0.0173', '0.02446', '0.02756', '0.004986', '0.001173', '0.02722', '0.002466', '-0.0004065', '0.06323', '0.02127', '0.02806', '-0.03049', '0.008675', '0.00415']",,,,,,,
mondo:0014138,nemaline myopathy 8,"['nemaline myopathy caused by mutation in KLHL40', 'nemaline myopathy type 8', 'KLHL40 nemaline myopathy', 'nemaline myopathy 8', 'NEM8', 'nemaline myopathy 8, autosomal recessive']",0110930,615348,,C3809209,,C129871,,,,,,
mondo:0014139,"Ehlers-Danlos syndrome, spondylodysplastic type, 2","['B3GALT6 Ehlers-Danlos syndrome progeroid type', 'B3GALT6-related spEDS', 'EDSP2', 'Ehlers-Danlos syndrome, progeroid type, 2, formerly', 'Ehlers-Danlos syndrome progeroid type 2', 'Ehlers-Danlos syndrome progeroid type caused by mutation in B3GALT6', 'spEDS-B3GALT6', 'Ehlers-Danlos syndrome, progeroid type, 2', 'Ehlers-Danlos syndrome, spondylodysplastic type, 2', 'B3GALT6-related spondylodysplastic EDS', 'EDSSPD2', 'Beta3GalT6-deficient EDS']",,615349,536467,C3809210,,,,,,,,
mondo:0014140,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A14","['Walker-Warburg syndrome or muscle-eye-brain disease, GMPPB-related', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 14', 'MDDGA14', 'muscle-eye-brain-GMPPB related']",0111233,615350,,C3809216,,,,,,,,
mondo:0014141,"muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B14","['muscular dystrophy, congenital, GMPPB-related', 'congenital muscular dystrophy-GMPPB related', 'muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 14', 'muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 14', 'MDDGB14']",0112377,615351,370968,C3809221,,,,,,,,
mondo:0014142,autosomal recessive limb-girdle muscular dystrophy type 2T,"['muscular dystrophy-dystroglycanopathy (limb-girdle) type C14', 'limb-girdle muscular dystrophy type 2T', 'GMPPB autosomal recessive limb-girdle muscular dystrophy', 'LGMD-GMPPB related', 'muscular dystrophy-dystroglycanopathy limb-girdle GMPPB-related', 'muscular dystrophy, limb-girdle, type 2T', 'muscular dystrophy limb-girdle type 2T', 'muscular dystrophy-dystroglycanopathy, limb-girdle, GMPPB-related', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in GMPPB', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 14', 'LGMD2T', 'MDDGC14']",0110294,615352,363623,C3714932,"['0.06586', '-0.5415', '-0.567', '-0.3105', '0.5884', '-1.265', '0.0663', '1.012', '-1.786', '-0.726', '-0.0937', '0.355', '-0.364', '0.991', '0.0661', '0.1844', '-0.705', '-0.6084', '-0.2217', '-0.6475', '0.1571', '0.1488', '0.11694', '0.5654', '0.085', '-0.1663', '-0.2303', '-0.695', '0.266', '-0.0939', '0.8994', '-0.1333', '0.757', '0.2191', '0.1161', '0.0652', '-0.588', '0.0912', '-0.1195', '-0.3118', '0.2588', '-0.13', '-0.2683', '0.3562', '-0.2903', '0.2964', '0.2617', '0.6953', '-0.0397', '0.4927', '0.251', '-0.3271', '0.2666', '-0.7607', '0.2788', '-0.651', '0.5015', '1.092', '-0.1626', '-0.0664', '0.222', '-0.083', '-0.0969', '0.08606', '0.1188', '0.2053', '-0.0369', '0.724', '-0.49', '-0.3308', '-0.09015', '0.452', '0.1821', '0.045', '0.5938', '0.3948', '0.12103', '0.152', '-0.0715', '0.2495', '0.07214', '0.1886', '-0.1414', '0.08466', '-0.1015', '0.2206', '-0.2491', '-0.2488', '1.087', '0.2273', '-0.2864', '0.161', '0.3293', '0.9243', '0.1312', '0.2583', '0.2703', '-0.3735', '0.1096', '-0.02419']",,,,,,,
mondo:0014143,Noonan syndrome 8,"['Noonan syndrome caused by mutation in RIT1', 'Noonan syndrome 8', 'Noonan syndrome type 8', 'RIT1 Noonan syndrome', 'NS8']",0060586,615355,,C3809233,,C176936,,,,,,
mondo:0014144,autosomal recessive limb-girdle muscular dystrophy type R18,"['muscular dystrophy, limb-girdle, type 2S', 'TRAPPC11 autosomal recessive limb-girdle muscular dystrophy', 'limb-girdle muscular dystrophy type 2S', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in TRAPPC11', 'LGMD2S', 'muscular dystrophy, limb-girdle, autosomal recessive 18', 'autosomal recessive limb-girdle muscular dystrophy type 2S']",0110287,615356,369840,C3809236,"['-0.2534', '-0.519', '-0.4163', '-0.0869', '0.777', '-1.094', '0.1892', '0.7666', '-1.592', '-0.819', '-0.081', '0.428', '-0.4622', '0.8364', '0.216', '0.2783', '-0.533', '-0.476', '-0.1252', '-0.552', '0.2034', '0.1866', '0.142', '0.6304', '-0.0442', '0.182', '-0.3113', '-1.06', '0.158', '-0.01468', '0.564', '-0.1473', '0.9463', '0.326', '0.1439', '0.09674', '-0.803', '0.003235', '-0.1953', '-0.1776', '0.2756', '-0.12146', '-0.4778', '0.4946', '-0.2257', '0.493', '0.1562', '0.7856', '-0.2742', '0.8057', '0.1611', '-0.2588', '0.3623', '-0.8037', '0.2388', '-0.837', '0.1901', '0.857', '-0.1608', '-0.1223', '0.4048', '-0.1306', '-0.0696', '-0.01962', '-0.1835', '0.04868', '0.10443', '0.519', '-0.2202', '-0.4136', '0.06665', '0.6943', '0.04907', '-0.0423', '0.5483', '0.6797', '0.3289', '0.223', '-0.1171', '0.2551', '0.06683', '-0.1058', '-0.02615', '0.3708', '-0.1829', '0.2908', '-0.0671', '-0.10175', '0.9785', '0.4587', '-0.1631', '0.4475', '0.2502', '0.9824', '0.1576', '-0.009735', '0.3503', '-0.0005217', '-0.04462', '-0.1176']",,,,,,,
mondo:0014145,Leber congenital amaurosis 17,"['Leber congenital amaurosis caused by mutation in GDF6', 'Leber congenital amaurosis type 17', 'LCA17', 'GDF6 Leber congenital amaurosis', 'Leber congenital amaurosis 17']",0110217,615360,,C3715164,,,,,,H35.5,,
mondo:0014146,autosomal dominant hypocalcemia 2,"['hypocalcemia, autosomal dominant type 2', 'hypocalcemia, autosomal dominant 2', 'HYPOC2', 'autosomal dominant hypocalcemia type 2']",0090108,615361,,C3809243,,,,,,,,
mondo:0014147,neuronal ceroid lipofuscinosis 13,"['neuronal ceroid lipofuscinosis type 13', 'CLN13 disease', 'ceroid lipofuscinosis, neuronal, 13, Kufs type', 'neuronal ceroid lipofuscinosis caused by mutation in CTSF', 'ceroid lipofuscinosis, neuronal, type 13', 'ceroid lipofuscinosis, neuronal, 13', 'CTSF neuronal ceroid lipofuscinosis', 'neuronal ceroid lipofuscinosis 13 Kufs type', 'CLN13', 'ceroid lipofuscinosis, neuronal, 13 (Kufs type)']",0110727,615362,352709,C3715049,"['0.188', '0.6562', '-0.3013', '0.0848', '0.465', '-1.228', '0.02951', '0.4573', '-0.3052', '0.1426', '-0.757', '-0.045', '-0.1199', '0.0889', '0.5127', '-0.583', '-0.05524', '-0.479', '0.07965', '-0.1766', '0.1473', '-0.379', '-0.04248', '-0.1787', '0.2319', '-0.2969', '-0.583', '-0.2678', '-0.73', '0.3906', '1.089', '-0.1908', '0.497', '-0.3057', '0.592', '0.2037', '-0.995', '0.518', '-0.3342', '-0.005543', '-0.1434', '-0.2551', '1.025', '-0.1713', '0.01097', '-0.9326', '-0.1287', '-0.01403', '0.0661', '0.2324', '0.799', '0.4636', '-0.959', '0.0705', '0.671', '-1.37', '0.989', '-0.3584', '-0.5537', '-0.02759', '0.255', '-0.03372', '0.3813', '-0.1841', '0.5864', '-0.2324', '0.8154', '0.01561', '-0.2644', '0.3765', '-0.235', '0.2986', '-0.0758', '-0.8325', '0.2798', '0.2952', '-0.0197', '0.1698', '-0.7905', '-0.04788', '0.6045', '0.3303', '-0.5264', '0.1783', '0.551', '-0.5034', '0.3047', '1.089', '-0.08325', '0.344', '0.0946', '0.2935', '-0.5747', '0.0978', '0.333', '0.14', '0.6636', '-0.0767', '0.688', '-0.3716']",,,,,,,
mondo:0014148,estrogen resistance syndrome,"['oestrogen resistance', 'estrogen resistance', 'ESTRR', 'oestrogen insensitivity', 'estrogen insensitivity']",,615363,785,C3809250,,,0009042,,,,,
mondo:0014149,fetal akinesia-cerebral and retinal hemorrhage syndrome,"['LCCS5', 'myopathy, centronuclear, lethal, autosomal recessive', 'lethal congenital contracture syndrome 5', 'lethal congenital contracture syndrome type 5']",,615368,363409,C3809272,"['-0.876', '0.11743', '0.1348', '-0.4482', '0.1019', '-0.353', '-0.01793', '0.6807', '-0.5522', '-0.1376', '-0.2769', '-0.10876', '0.0773', '0.002518', '-0.1575', '-0.07007', '0.2404', '0.5024', '-0.2413', '-0.9785', '0.316', '-0.281', '0.4197', '0.02814', '0.1545', '0.0809', '0.010414', '0.1252', '0.1897', '0.2837', '-0.1189', '-0.2974', '0.808', '0.507', '-0.2766', '0.0854', '-0.07733', '-0.1772', '-0.11487', '-0.1409', '-0.156', '0.00961', '-0.1356', '-0.1143', '-0.02272', '0.1423', '-0.2175', '0.4607', '0.2742', '0.1199', '-0.04282', '-0.2015', '0.256', '-0.4482', '-0.11304', '-0.303', '0.1827', '-0.3936', '0.05173', '0.04706', '0.3618', '-0.04025', '-0.2465', '-0.1656', '-0.36', '-0.2274', '0.4932', '0.2883', '-0.568', '0.5747', '-0.2069', '0.1691', '-0.1091', '-0.1973', '-0.0913', '-0.392', '0.4294', '0.2053', '-0.1294', '-0.3506', '-0.4175', '-0.1205', '0.4763', '0.4019', '-0.4636', '0.061', '0.1831', '0.4617', '0.1632', '-0.3867', '0.1761', '0.467', '0.3955', '0.5522', '0.2104', '0.5063', '0.5537', '-0.177', '0.3506', '0.2365']",,,,,,,
mondo:0014150,developmental and epileptic encephalopathy 94,"['CHCHD10-related disorders', 'EEOC', 'childhood-onset epileptic encephalopathy', 'childhood onset epileptic encephalopathy', 'DEE94', 'epileptic encephalopathy, childhood-onset', 'developmental and epileptic encephalopathy 94', 'CHD2 myoclonic encephalopathy']",0081325,615369,,C3809278,,,,,,,,
mondo:0014151,"pulmonary hypertension, neonatal, susceptibility to","['susceptibility to neonatal pulmonary hypertension', 'PHN', 'pulmonary hypertension, neonatal, susceptibility to']",,615371,,C0032768,,,,,,,,
mondo:0014152,left ventricular noncompaction 8,"['familial isolated dilated cardiomyopathy caused by mutation in PRDM16', 'left ventricular noncompaction type 8', 'cardiomyopathy, dilated, 1Ll', 'LVNC8', 'PRDM16 familial isolated dilated cardiomyopathy', 'left ventricular noncompaction 8']",0081157,615373,,C3809288,,,,,,,,
mondo:0014153,cone-rod dystrophy 18,"['CORD18', 'cone-rod dystrophy type 18', 'cone-rod dystrophy 18', 'cone-rod dystrophy caused by mutation in RAB28', 'RAB28 cone-rod dystrophy']",0111024,615374,,C3809299,,,,,,,,
mondo:0014154,Charcot-Marie-Tooth disease recessive intermediate C,"['Charcot-Marie-Tooth disease caused by mutation in PLEKHG5', 'autosomal recessive intermediate Charcot-Marie-Tooth disease type C', 'Charcot-Marie-Tooth disease recessive intermediate type C', 'PLEKHG5 Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth neuropathy, recessive Intermediate C', 'Charcot-Marie-Tooth disease, recessive intermediate C', 'RI-CMTC', 'Charcot-Marie-Tooth disease, recessive Intermediate type C', 'RI-CMT type C', 'CMTRIC']",0110198,615376,369867,C3809309,"['0.1813', '0.2363', '0.2847', '-0.1666', '-0.02997', '-0.2754', '-0.2522', '0.481', '-0.829', '-0.1198', '-0.04413', '0.2595', '-0.263', '0.1323', '-0.09827', '-0.3535', '-0.3176', '-0.6157', '-0.4524', '-0.7275', '0.15', '0.1411', '0.3545', '0.7983', '0.1677', '0.594', '-0.03119', '0.1542', '-0.0827', '-0.4524', '-0.01575', '-0.4556', '0.3225', '0.1912', '0.26', '-0.7495', '-0.565', '-0.2986', '0.3958', '-0.3323', '-1.365', '-0.48', '-0.4775', '0.71', '-0.3538', '-0.2886', '0.06714', '0.0822', '-0.2234', '-0.0989', '-0.02296', '0.1755', '-0.1509', '-0.957', '-0.01912', '-0.4111', '-0.1538', '0.3284', '-0.8936', '-0.0931', '-0.4998', '-0.02673', '0.8857', '0.8384', '-1.053', '1.026', '-0.0688', '0.765', '-0.8267', '0.53', '-0.9263', '0.3008', '0.3416', '-0.0828', '1.179', '0.6006', '-0.285', '0.3713', '0.3005', '-0.2961', '-0.10535', '-0.0808', '0.7676', '0.6567', '0.2598', '0.1214', '0.1411', '0.6885', '0.7676', '0.2612', '0.144', '-0.1952', '0.02428', '0.5312', '0.4453', '0.728', '0.9287', '-0.592', '-0.05264', '0.2607']",,,,,,,
mondo:0014155,"atrial fibrillation, familial, 13","['SCN1B familial atrial fibrillation', 'atrial fibrillation, familial, type 13', 'atrial fibrillation, familial, 13', 'ATFB13', 'familial atrial fibrillation caused by mutation in SCN1B']",,615377,,C3809311,,,,,,,,
mondo:0014156,"atrial fibrillation, familial, 14","['SCN2B familial atrial fibrillation', 'atrial fibrillation, familial, 14', 'ATFB14', 'familial atrial fibrillation caused by mutation in SCN2B', 'atrial fibrillation, familial, type 14']",,615378,,C3809312,,,,,,,,
mondo:0014157,mandibular hypoplasia-deafness-progeroid syndrome,"['MDPL', 'mandibular hypoplasia-hearing loss-progeroid syndrome', 'MDP syndrome', 'mandibular hypoplasia, deafness, progeroid features', 'mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome']",,615381,363649,C3715192,"['-0.0746', '0.05786', '0.3862', '-0.2279', '0.2544', '-0.2964', '0.08923', '0.4666', '-0.2817', '0.03497', '-0.0873', '0.0285', '-0.0712', '-0.1743', '-0.4324', '-0.163', '0.263', '0.06903', '-0.3794', '-0.2515', '-0.0494', '-0.4583', '0.1694', '-0.2463', '0.1362', '0.06903', '-0.07794', '-0.05035', '0.2766', '-0.475', '0.353', '0.0168', '0.3801', '0.01697', '0.123', '0.1272', '-0.1454', '0.08545', '-0.2303', '-0.43', '0.2397', '-0.010544', '-0.3496', '0.08887', '0.1592', '-0.1617', '0.3315', '0.3267', '-0.08356', '-0.1018', '-0.256', '0.1118', '0.2698', '0.2092', '-0.3645', '-0.2588', '-0.02975', '-0.3328', '-0.1353', '-0.2085', '0.137', '0.1007', '-0.3787', '-0.05737', '0.0687', '-0.0668', '0.1382', '0.5166', '-0.2139', '0.3994', '-0.3914', '0.2979', '0.4314', '0.0995', '-0.06445', '-0.2986', '0.0855', '0.0624', '-0.2869', '-0.0786', '-0.0184', '-0.0999', '-0.06256', '0.3357', '-0.12146', '0.1209', '-0.03796', '0.06082', '0.2324', '-0.003387', '0.258', '0.5317', '0.08215', '0.2009', '0.284', '0.04855', '0.292', '0.0701', '0.2294', '0.2683']",,,,,,,
mondo:0014158,nephronophthisis 16,"['autosomal recessive infantile nephronophthisis', 'NPHP16', 'ANKS6 nephronophthisis (disease)', 'infantile nephronophthisis', 'nephronophthisis type 16', 'nephronophthisis 16', 'autosomal recessive infantile NPHP']",0111124,615382,93591,C3809320,,,,,,,,
mondo:0014159,autosomal recessive spinocerebellar ataxia 14,"['spinocerebellar ataxia, autosomal recessive 14', 'SPARCA', 'SPARCA1', 'spinocerebellar ataxia, autosomal recessive type 14', 'SPTBN2 autosomal recessive cerebellar ataxia', 'autosomal recessive cerebellar ataxia caused by mutation in SPTBN2', 'autosomal recessive cerebellar ataxia-cognitive defect syndrome', 'SCAR14', 'spectrin-associated autosomal recessive cerebellar ataxia type 1', 'autosomal recessive spinocerebellar ataxia type 14', 'spectrin-associated autosomal recessive cerebellar ataxia', 'infantile-onset spinocerebellar ataxia-psychomotor delay syndrome', 'cerebellar ataxia, autosomal recessive, spectrin-associated, 1', 'Ataxie spinocérébelleuse à début infantile avec retard psychomoteur']",0080058,615386,352403,C3809327,"['-0.2551', '-0.3394', '-0.06537', '0.04562', '-0.1638', '-0.9697', '0.166', '0.03818', '-0.688', '-0.9893', '0.1171', '0.272', '-0.2646', '0.12427', '0.531', '-0.4216', '-0.2786', '-0.3555', '0.02068', '-1.131', '-0.04227', '-0.2205', '0.12225', '-0.722', '0.541', '-0.5396', '-0.2646', '0.1521', '-0.2104', '-0.9565', '0.1583', '0.5464', '-0.5957', '-0.1582', '0.3', '0.00494', '-0.2198', '0.3306', '0.52', '0.3408', '0.4778', '0.3784', '-0.3718', '0.5586', '0.3599', '-0.634', '0.05392', '0.5186', '0.4985', '-0.1448', '-0.2241', '0.1501', '-0.153', '-0.3362', '-0.0092', '-0.823', '0.1829', '0.5693', '-0.104', '0.517', '-0.5186', '0.2122', '0.305', '-0.1556', '-0.4146', '0.3975', '0.2659', '0.4785', '-0.45', '0.4563', '0.802', '0.4534', '-0.01717', '-0.701', '0.7603', '0.406', '0.2568', '0.3572', '0.1278', '0.763', '-0.3762', '-0.791', '0.4058', '0.914', '-0.2986', '-0.769', '0.17', '0.0574', '0.5757', '0.803', '0.4167', '0.5386', '0.1252', '0.2052', '1.152', '1.002', '0.4797', '0.436', '-0.3708', '-0.2205']",,,,,,,
mondo:0014160,TCR-alpha-beta-positive T-cell deficiency,"['T-cell receptor-ALPHA/BETA deficiency', 'immunodeficiency 7, TCR-alpha/beta deficient', 'immunodeficiency 7', 'TCR-alpha-beta+ T-cell deficiency', 'TCR-Alpha/Beta deficiency', 'IMD7']",0111977,615387,397959,C3809332,"['-0.1926', '0.0994', '0.2651', '-0.529', '-0.2141', '-0.4395', '0.1641', '-0.2466', '0.3354', '-0.01173', '0.2086', '0.1744', '-0.3594', '-0.05325', '-0.1759', '0.1875', '0.1888', '0.02383', '-0.3901', '-0.6895', '-0.1715', '-0.3225', '0.4817', '-0.239', '0.011734', '-0.154', '-0.1052', '0.04004', '0.0623', '-0.6274', '0.1732', '0.03114', '0.384', '0.2927', '0.3518', '-0.02635', '-0.8193', '-0.01262', '-0.4707', '-0.2206', '-0.3276', '-0.02682', '0.3398', '-0.0688', '0.1317', '-0.2996', '0.1929', '-0.1617', '-0.357', '0.2104', '-0.303', '0.31', '0.3157', '0.1669', '-0.3765', '0.2805', '-0.1079', '-0.4563', '-0.2668', '0.2089', '0.2242', '0.2542', '-0.179', '0.1908', '0.4321', '-0.2263', '0.5234', '0.578', '-0.02412', '0.839', '-0.3467', '-0.2573', '-0.1642', '-0.283', '-0.0671', '-0.02031', '0.3093', '-0.0881', '0.3398', '0.3118', '-0.006638', '-0.39', '-0.07117', '0.1725', '-0.05457', '-0.11725', '0.1014', '0.1656', '0.4102', '0.144', '0.613', '0.3313', '-0.09503', '-0.1703', '0.8247', '0.8657', '0.2067', '-0.2993', '0.197', '-0.05713']",,,,,,,
mondo:0014161,vesicoureteral reflux 7,"['VUR7', 'vesicoureteral reflux 7']",,615390,,C3809337,,,,,,,,
mondo:0014162,infantile hypertrophic cardiomyopathy due to MRPL44 deficiency,"['combined oxidative phosphorylation deficiency caused by mutation in MRPL44', 'COXPD16', 'combined oxidative phosphorylation deficiency type 16', 'combined oxidative phosphorylation deficiency 16', 'MRPL44 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation defect type 16']",0111469,615395,352563,C3809339,"['-0.2605', '-0.339', '-0.271', '1.091', '-0.1598', '-0.05515', '0.1333', '1.285', '-0.3896', '-0.1572', '0.3308', '-0.5576', '-0.2401', '0.098', '-0.805', '-0.575', '-0.7363', '-0.6953', '-0.6826', '-0.8496', '0.46', '-0.0398', '0.1665', '0.4355', '-0.4397', '-0.02118', '-0.0869', '0.3289', '0.1355', '0.2003', '0.814', '-0.1661', '0.3896', '-0.05017', '-0.1501', '0.1757', '-0.1302', '0.0952', '0.3674', '-0.4941', '0.4934', '-0.1953', '0.433', '0.4546', '-0.014534', '0.1825', '-0.5884', '0.4595', '-0.3455', '-0.4573', '0.08466', '-0.03912', '-0.1791', '0.5923', '0.3406', '-0.645', '-0.3228', '1.063', '0.04663', '-0.4717', '-0.05505', '0.3508', '0.4639', '-0.406', '-0.6587', '0.0837', '0.2979', '0.579', '-0.6353', '0.457', '-0.05078', '0.4834', '0.724', '-0.3083', '-0.152', '0.1781', '0.01886', '-0.1854', '0.2551', '0.7993', '0.813', '-0.227', '-0.0883', '-0.467', '0.687', '-0.4858', '0.778', '0.3564', '0.63', '0.404', '0.3638', '-0.381', '-0.5737', '0.407', '0.968', '0.705', '0.5005', '-0.04868', '-0.63', '0.3242']",,,,,,,
mondo:0014163,left ventricular noncompaction 10,"['left ventricular noncompaction 10', 'LVNC10', 'MYBPC3 left ventricular noncompaction', 'cardiomyopathy, dilated, 1Mm', 'left ventricular noncompaction caused by mutation in MYBPC3', 'left ventricular noncompaction type 10']",,615396,,C3715165,,,,,,,,
mondo:0014164,"Meckel syndrome, type 11","['TMEM231 Meckel syndrome', 'MKS11', 'Meckel syndrome, type 11', 'Meckel syndrome caused by mutation in TMEM231', 'meckel syndrome 11']",,615397,,C3809352,,,,,,,,
mondo:0014165,multiple congenital anomalies-hypotonia-seizures syndrome 3,"['light fixation seizure syndrome', 'congenital disorder of glycosylation due to PIGT deficiency', 'MCAHS type 3', 'glycosylphosphatidylinositol biosynthesis defect 7', 'M syndrome', 'MCAHS3', 'multiple congenital anomalies-hypotonia-seizures syndrome 3', 'PIGT multiple congenital anomalies/dysmorphic syndrome-intellectual disability', 'PIGT-CDG', 'intellectual disability-seizures-hypotonia-ophthalmologic-skeletal anomalies syndrome', 'multiple congenital anomalies-hypotonia-seizures syndrome type 3', 'multiple congenital anomalies/dysmorphic syndrome-intellectual disability caused by mutation in PIGT', 'LFSS']",0080140,615398,369837,C3809356,"['-0.1148', '-0.173', '0.2402', '0.245', '-0.5454', '-0.1512', '0.7354', '0.3328', '-0.4114', '-0.266', '-0.3958', '-0.1488', '0.1722', '0.3892', '-0.5254', '0.4517', '0.04944', '-0.161', '-0.211', '-0.3113', '0.11', '0.98', '0.02623', '-0.2566', '0.12195', '-0.186', '-0.0714', '0.08203', '-0.304', '0.478', '-0.03702', '-0.03041', '0.3496', '0.4922', '0.513', '0.3438', '-0.05655', '-0.2267', '0.01985', '-0.4075', '-0.1619', '-0.1703', '-0.3682', '-0.3364', '0.04694', '-0.2886', '0.1069', '0.8457', '-0.08813', '0.868', '-0.0723', '0.1355', '0.2393', '-0.5215', '-0.0499', '-0.005196', '-0.3357', '0.09283', '-0.2443', '0.2147', '0.003027', '0.412', '0.1887', '-0.05087', '-0.541', '0.7505', '0.0711', '0.1774', '-0.7134', '0.8506', '0.2445', '0.711', '0.1625', '-0.2527', '0.236', '0.701', '1.086', '0.06323', '-0.3174', '0.06964', '0.302', '0.909', '0.4678', '0.24', '0.2312', '0.187', '-0.1716', '0.766', '0.4954', '1.106', '0.0666', '0.5107', '0.3013', '0.0766', '-0.0849', '0.193', '0.412', '-0.275', '0.2499', '0.556']",,,C566367,,,,
mondo:0014166,paroxysmal nocturnal hemoglobinuria 2,"['paroxysmal nocturnal hemoglobinuria type 2', 'paroxysmal nocturnal hemoglobinuria 2', 'PNH2', 'PIGT paroxysmal nocturnal hemoglobinuria', 'paroxysmal nocturnal hemoglobinuria caused by mutation in PIGT', 'paroxysmal nocturnal hemoglobinuria 2, autosomal dominant, somatic mutation']",,615399,,C3809369,,,,,,,,
mondo:0014167,"epilepsy, familial adult myoclonic, 5","['epilepsy, familial adult myoclonic caused by mutation in CNTN2', 'epilepsy, familial ADULT myoclonic, 5', 'CNTN2 epilepsy, familial adult myoclonic', 'FAME5', 'epilepsy, familial adult myoclonic, 5', 'epilepsy, familial adult myoclonic, type 5', 'epilepsy, myoclonic, familial adult, 5', 'cortical myoclonic tremor with epilepsy, familial, 5']",0111691,615400,,C3809374,,,,,,,,
mondo:0014168,severe combined immunodeficiency due to CORO1A deficiency,"['IMD8', 'immunodeficiency type 8', 'immunodeficiency 8', 'SCID due to CORO1A deficiency', 'severe combined immunodeficiency due to coronin-1A deficiency', 'coronin-1A deficiency', 'SCID due to coronin-1A deficiency']",0060019,615401,228003,C3809383,"['-0.12384', '0.1271', '0.05286', '-0.01933', '0.0677', '-0.1189', '0.06573', '0.1708', '-0.0873', '-0.11566', '-0.03876', '0.001832', '-0.02573', '0.02934', '0.002317', '-0.0869', '0.0373', '0.0284', '-0.1732', '-0.298', '-0.0839', '-0.1342', '0.1561', '-0.04227', '-0.01646', '-0.0287', '-0.0565', '-0.0384', '0.01184', '-0.1409', '0.1047', '0.1263', '0.26', '0.06647', '0.00617', '-0.1313', '-0.0413', '-0.1279', '-0.04654', '-0.2063', '0.0712', '-0.1461', '0.0297', '-0.06757', '-0.1403', '-0.0783', '-0.01599', '0.052', '0.0439', '0.0695', '-0.04285', '-0.1257', '0.11383', '0.02834', '-0.1962', '0.03262', '0.09326', '-0.0721', '-0.1344', '0.05072', '0.1042', '0.1131', '0.02364', '0.01599', '0.1168', '0.02155', '0.1586', '0.10254', '-0.1826', '0.1534', '-0.1564', '-0.013824', '-0.01004', '-0.1486', '0.0886', '0.03787', '0.0668', '-0.007732', '0.00815', '0.0395', '-0.01516', '0.012764', '-0.04767', '0.1357', '0.03973', '-0.00528', '0.1367', '0.172', '0.272', '0.03714', '0.146', '0.1225', '-0.08264', '-0.000505', '0.3367', '0.1746', '0.1254', '-0.28', '0.04095', '0.1024']",,,,,,,
mondo:0014169,dyschromatosis universalis hereditaria 3,"['dyschromatosis universalis hereditaria 3', 'DUH3', 'dyschromatosis universalis hereditaria type 3', 'dyschromatosis universalis hereditaria caused by mutation in ABCB6', 'ABCB6 dyschromatosis universalis hereditaria']",,615402,,C3809394,,,,,,,,
mondo:0014170,complex cortical dysplasia with other brain malformations 3,"['cortical dysplasia, Complex, with Other brain malformations type 3', 'CDCBM3', 'KIF2A complex cortical dysplasia with other brain malformations', 'complex cortical dysplasia with other brain malformations caused by mutation in KIF2A', 'cortical dysplasia, complex, with other brain malformations 3', 'complex cortical dysplasia with other brain malformations type 3']",0090134,615411,,C3809414,,,,,,,,
mondo:0014171,complex cortical dysplasia with other brain malformations 4,"['cortical dysplasia, complex, with other brain malformations 4', 'TUBG1 complex cortical dysplasia with other brain malformations', 'complex cortical dysplasia with other brain malformations caused by mutation in TUBG1', 'CDCBM4', 'cortical dysplasia, Complex, with Other brain malformations type 4', 'complex cortical dysplasia with other brain malformations type 4']",0090138,615412,,C3809420,,,,,,,,
mondo:0014172,spermatogenic failure 12,"['SPGF12', 'spermatogenic failure 12', 'NANOS1 azoospermia', 'spermatogenic failure type 12', 'azoospermia caused by mutation in NANOS1']",0070171,615413,,C3809427,,,,,,,,
mondo:0014173,"microcephaly 11, primary, autosomal recessive","['microcephaly 11, primary, autosomal recessive', 'autosomal recessive primary microcephaly caused by mutation in PHC1', 'MCPH11', 'PHC1 autosomal recessive primary microcephaly']",0070287,615414,,C3809431,,,,,,,,
mondo:0014174,renal-hepatic-pancreatic dysplasia 2,"['RHPD2', 'renal-hepatic-pancreatic dysplasia 2', 'renal-hepatic-pancreatic dysplasia type 2', 'renal-hepatic-pancreatic dysplasia caused by mutation in NEK8', 'NEK8 renal-hepatic-pancreatic dysplasia']",,615415,,C3809434,,,,,,,,
mondo:0014175,"mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive","['MTDPS12', 'mitochondrial DNA depletion syndrome 12B (cardiomyopathic type) AR', 'mitochondrial DNA depletion syndrome type 12', 'mitochondrial DNA depletion syndrome 12 (cardiomyopathic type)', 'mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), autosomal recessive', 'mitochondrial DNA depletion syndrome 12B (cardiomyopathic type), AR', 'MTDPS12B']",0080335,615418,,C4321247,"['-0.09534', '0.1509', '0.0373', '0.0755', '0.0326', '-0.143', '0.0411', '0.1447', '-0.10425', '-0.0697', '0.004322', '-0.00896', '0.0827', '-0.002153', '-0.011635', '-0.10175', '-0.06232', '-0.0755', '-0.05594', '-0.2013', '0.01802', '-0.08704', '0.0425', '-0.01682', '0.07465', '-0.02565', '-0.06073', '0.00995', '-0.04947', '-0.03632', '0.05374', '0.068', '0.155', '0.02142', '-0.00586', '-0.03442', '-0.05273', '-0.0885', '-0.01822', '-0.09644', '0.05835', '-0.183', '-0.007336', '-0.02368', '-0.0399', '-0.1017', '-0.05664', '0.0557', '0.0842', '-0.01666', '-0.0916', '-0.01616', '-0.0313', '0.01303', '-0.0361', '-0.0801', '0.1528', '-0.01999', '-0.10443', '0.06064', '0.1301', '-0.03085', '0.05756', '0.02264', '-0.04456', '-0.0224', '0.1583', '0.08026', '-0.1495', '0.1593', '-0.0548', '0.004704', '0.02695', '0.00679', '0.04425', '0.0877', '-0.0001913', '0.00343', '-0.1221', '-0.04984', '0.00883', '0.0395', '-0.06757', '0.0921', '-0.002756', '0.02388', '0.09796', '0.1436', '0.1389', '0.0538', '0.1445', '0.07605', '-0.05115', '-0.004955', '0.1754', '0.10486', '0.1059', '-0.1782', '-0.02177', '0.03778']",C129977,,,,,,
mondo:0014176,"hypotonia, infantile, with psychomotor retardation and characteristic facies","['hypotonia, infantile, with psychomotor retardation and characteristic facies', 'IHPRF', 'IHPRF syndrome', 'hypotonia-speech impairment-severe cognitive delay syndrome', 'infantile hypotonia-psychomotor retardation-characteristic facies syndrome']",,,371364,CN204877,"['-0.0429', '0.0812', '0.05957', '-0.0395', '0.00866', '-0.1125', '0.02269', '0.1683', '-0.1042', '-0.04163', '-0.06854', '-0.02376', '0.01956', '0.02478', '0.00866', '-0.05508', '-0.01558', '-0.03111', '-0.06995', '-0.1907', '0.03262', '-0.012215', '0.0588', '-0.02321', '0.04352', '-0.0299', '-0.04108', '-0.01034', '-0.01005', '-0.0497', '0.06003', '-0.011314', '0.113', '0.04703', '0.01746', '-0.03995', '-0.02782', '-0.05582', '-0.01482', '-0.09064', '0.0681', '-0.08374', '0.005905', '-0.03041', '0.02054', '-0.09314', '-0.0278', '0.06824', '-6.03e-05', '0.0462', '-0.0793', '0.02203', '0.00907', '-0.01038', '-0.005108', '0.001254', '0.04633', '-0.05185', '-0.0991', '0.03766', '0.0384', '0.02202', '0.03008', '0.0017805', '-0.002445', '0.012634', '0.06525', '0.0939', '-0.112', '0.0957', '-0.0843', '0.03763', '0.03467', '-0.06525', '0.05136', '0.04715', '0.03564', '-0.01398', '-0.0641', '-0.06107', '0.01348', '-0.03577', '-0.0505', '0.1265', '0.015274', '0.0271', '0.005013', '0.09186', '0.1575', '0.05783', '0.0805', '0.11115', '-0.0194', '0.03156', '0.1676', '0.0932', '0.0754', '-0.105', '0.0405', '0.0629']",,,,,,,
mondo:0014177,"myopia 22, autosomal dominant","['MYP22', 'myopia 22, autosomal dominant']",,615420,,C3809464,,,,,,,,
mondo:0014178,inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2,"['inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA2B1', 'HNRNPA2B1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia', 'inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 2', 'IBMPFD2', 'multisystem Proteinopathy 2', 'inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 2']",0111384,615422,,C3809468,,,,,,,,
mondo:0014179,inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3,"['inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 3', 'multisystem Proteinopathy 3', 'HNRNPA1 inclusion body myopathy with Paget disease of bone and frontotemporal dementia', 'inclusion body myopathy with Paget disease of bone and frontotemporal dementia caused by mutation in HNRNPA1', 'inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 3', 'IBMPFD3', 'inclusion body myopathy with early-onset paget disease without frontotemporal dementia 3']",0111386,615424,,C3809469,,,,,,,,
mondo:0014180,"epidermolysis bullosa simplex 3, localized or generalized intermediate, with BP230 deficiency","['epidermolysis bullosa simplex, autosomal recessive type 2', 'epidermolysis bullosa simplex due to BP230 deficiency', 'epidermolysis bullosa simplex 3, localized or generalized intermediate, with bp230 deficiency', 'epidermolysis bullosa simplex, autosomal recessive 2', 'EBS-AR BP230', 'EBSB2', 'DST-related epidermolysis bullosa simplex', 'epidermolysis bullosa simplex 3, localised or generalised intermediate, with bp230 deficiency']",,615425,412181,C3809470,,,,,,,,
mondo:0014181,amyotrophic lateral sclerosis type 20,"['HNRNPA1 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis caused by mutation in HNRNPA1', 'amyotrophic lateral sclerosis type 20', 'amyotrophic lateral sclerosis 20', 'ALS20']",0060211,615426,,C3715156,,,,,,,,
mondo:0014182,autosomal recessive nonsyndromic hearing loss 88,"['autosomal recessive nonsyndromic deafness type 88', 'deafness, autosomal recessive 88', 'ELMOD3 autosomal recessive nonsyndromic deafness', 'DFNB88', 'autosomal recessive deafness 88', 'autosomal recessive nonsyndromic deafness caused by mutation in ELMOD3', 'deafness, autosomal recessive type 88', 'autosomal recessive nonsyndromic deafness 88']",0110533,615429,,C2829267,,,,,,,,
mondo:0014183,"myopia 23, autosomal recessive","['myopia 23, autosomal recessive', 'MYP23']",,615431,,C3809482,,,,,,,,
mondo:0014184,specific language impairment 5,"['SLI5', 'specific language impairment 5', 'specific language impairment type 5']",,615432,,C3809483,,,,,,,,
mondo:0014185,chromosome 3q13.31 deletion syndrome,"['Del(3)(q13)', 'chromosome 3q13.31 deletion syndrome', 'monosomy 3q13', '3q13 microdeletion syndrome']",0060418,615433,1621,CN036884,,,,C536808,,,,
mondo:0014186,retinitis pigmentosa with or without situs inversus,"['retinitis pigmentosa with or without situs inversus', 'retinitis pigmentosa caused by mutation in ARL2BP', 'ARL2BP retinitis pigmentosa']",0110419,615434,,C3809503,,,,,,H35.5,,
mondo:0014187,"aortic aneurysm, familial thoracic 8","['familial thoracic aortic aneurysm and aortic dissection caused by mutation in PRKG1', 'PRKG1 familial thoracic aortic aneurysm and aortic dissection', 'AAT8', 'aortic aneurysm, familial thoracic 8', 'aortic aneurysm, familial thoracic type 8']",,615436,,C3809513,,,,,,,,
mondo:0014189,age related macular degeneration 13,"['CFI age-related macular degeneration', 'age-related macular degeneration caused by mutation in CFI', 'age related macular degeneration type 13', 'macular Degeneration, age-related, type 13', 'macular degeneration, age-related, 13', 'macular degeneration, age-related, 13, susceptibility to', 'ARMD13']",0110025,615439,,C3809523,,,,,,,,
mondo:0014190,combined oxidative phosphorylation defect type 17,"['combined oxidative phosphorylation deficiency caused by mutation in ELAC2', 'ELAC2 combined oxidative phosphorylation deficiency', 'COXPD17', 'combined oxidative phosphorylation deficiency type 17', 'combined oxidative phosphorylation deficiency 17']",0111496,615440,369913,C3809526,"['-0.5728', '0.007545', '0.1398', '-0.10516', '0.00266', '-0.4912', '0.09607', '0.515', '-0.299', '0.0724', '-0.1854', '-0.1814', '-0.1111', '-0.2461', '0.04822', '-0.2097', '-0.0679', '-0.1592', '-0.1925', '-0.675', '0.3794', '-0.0724', '0.2976', '-0.005047', '0.015076', '-0.1002', '0.2257', '0.1299', '-0.1178', '-0.1692', '0.2023', '0.3252', '0.7007', '0.25', '-0.03635', '-0.7085', '0.01267', '-0.04495', '-0.1072', '-0.1987', '-0.002754', '-0.1714', '0.01587', '0.4011', '-0.4253', '-0.146', '0.0281', '0.1713', '-0.10333', '-0.1951', '-0.2401', '-0.158', '0.0636', '-0.09753', '-0.3394', '-0.2363', '0.2001', '-0.0179', '-0.08514', '0.4443', '0.03079', '0.01854', '0.4421', '-0.222', '-0.296', '0.0169', '0.1753', '0.4543', '-0.559', '0.0806', '-0.323', '0.094', '0.11017', '-0.0633', '0.2615', '-0.0884', '0.05884', '-0.2351', '0.03897', '0.532', '0.2384', '0.0991', '0.04416', '-0.09937', '-0.00502', '-0.04126', '0.4092', '0.4932', '0.468', '0.276', '0.3958', '0.04712', '-0.003813', '0.02135', '0.793', '0.4487', '0.3254', '-0.4001', '0.1136', '-0.1028']",,,,,,,
mondo:0014191,catecholaminergic polymorphic ventricular tachycardia 5,"['CPVT5', 'cardiac arrhythmia syndrome, with or without skeletal muscle weakness', 'TRDN catecholaminergic polymorphic ventricular tachycardia', 'catecholaminergic polymorphic ventricular tachycardia caused by mutation in TRDN', 'catecholaminergic polymorphic ventricular tachycardia type 5', 'CVPT5', 'ventricular tachycardia, catecholaminergic polymorphic, 5, with or without muscle weakness']",0060679,615441,,C3809536,,,,,,I47.2,,
mondo:0014192,primary ciliary dyskinesia 22,"['ZMYND10 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, type 22', 'primary ciliary dyskinesia 22 with or without situs inversus', 'ciliary dyskinesia, primary, 22, with or without situs inversus', 'primary ciliary dyskinesia type 22', 'primary ciliary dyskinesia caused by mutation in ZMYND10', 'CILD22', 'ciliary dyskinesia, primary, 22']",0110597,615444,,C3809543,,,,,,,,
mondo:0014193,primary ciliary dyskinesia 23,"['primary ciliary dyskinesia 23 with or without situs inversus', 'primary ciliary dyskinesia type 23', 'ciliary dyskinesia, primary, type 23', 'primary ciliary dyskinesia caused by mutation in ARMC4', 'CILD23', 'ARMC4 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 23', 'ciliary dyskinesia, primary, 23, with or without situs inversus']",0110609,615451,,C3809548,,,,,,,,
mondo:0014194,mitochondrial complex III deficiency nuclear type 6,"['mitochondrial Complex 3 deficiency, nuclear type 6', 'mitochondrial complex III deficiency, nuclear type 6', 'MC3DN6', 'CYC1 mitochondrial complex III deficiency', 'mitochondrial complex III deficiency caused by mutation in CYC1']",0080115,615453,,C3809553,,,,,,,,
mondo:0014195,microcornea-myopic chorioretinal atrophy,"['MMCAT syndrome', 'MMCAT', 'microcornea-myopic chorioretinal atrophy-telecanthus syndrome', 'microcornea, myopic chorioretinal atrophy, and telecanthus']",,615458,369970,C3809567,"['-0.224', '-0.02899', '0.2166', '-0.1816', '0.0772', '-0.2228', '-0.0359', '0.3005', '-0.4138', '-0.0762', '-0.1879', '-0.2244', '-0.1287', '-0.169', '-0.2693', '-0.1575', '0.2559', '-0.011635', '0.08856', '-0.5283', '-0.0958', '0.008606', '-0.003204', '0.0004833', '0.10895', '0.02563', '-0.2905', '0.197', '0.2251', '-0.0516', '0.2043', '0.00977', '0.3655', '0.3254', '0.09607', '0.01605', '-0.0921', '-0.2429', '-0.1715', '-0.4138', '0.2126', '0.00866', '0.02765', '-0.05753', '-0.09406', '-0.0448', '0.2225', '0.2157', '-0.1476', '-0.07367', '-0.03748', '0.2024', '-0.09515', '-0.3213', '-0.1571', '-0.3582', '0.3398', '-0.06216', '-0.1981', '0.0971', '0.2252', '-0.0485', '-0.1699', '0.2046', '0.0455', '-0.06976', '0.4272', '0.4844', '-0.02313', '0.3394', '-0.273', '0.2373', '0.10394', '-0.1074', '0.0715', '-0.3008', '0.168', '-0.1735', '-0.10834', '0.02295', '0.2064', '-0.1277', '-0.0923', '0.6333', '-0.04697', '-0.1774', '0.006268', '0.2788', '0.2256', '0.2676', '0.1895', '0.4941', '0.1592', '0.0689', '0.534', '-0.10834', '0.4714', '-0.041', '0.005295', '0.2428']",,,,,,,
mondo:0014196,Hartsfield-Bixler-Demyer syndrome,"['holoprosencephaly-ectrodactyly-cleft lip/palate syndrome', 'HRTFDS', 'HARTSFIELD syndrome', 'holoprosencephaly-ectrodactyly-cleft lip palate syndrome', 'holoprosencephaly, ectrodactyly, and bilateral cleft Lip/palate']",,615465,2117,C1845146,"['0.1941', '0.1482', '0.2954', '-0.1066', '0.4832', '-0.07983', '0.1231', '0.6064', '-0.561', '-1.368', '-0.697', '-0.4216', '0.4275', '0.3916', '-0.0623', '-0.2148', '-0.1661', '-0.2505', '-0.8296', '-0.4546', '0.3', '0.02397', '0.596', '-0.4546', '0.2266', '-0.2223', '0.05978', '0.05652', '0.10254', '-0.3044', '0.2896', '-0.1171', '0.6006', '-0.00979', '0.02266', '0.1305', '-0.138', '-0.222', '-0.1958', '0.3699', '-0.06775', '0.2573', '0.05997', '-0.38', '0.2627', '-0.2489', '0.5293', '0.07947', '-0.3909', '0.4207', '-0.3704', '-0.03726', '-0.104', '-0.02556', '-0.2566', '0.335', '-0.002863', '0.07935', '-0.1437', '0.384', '-0.1113', '0.443', '0.3684', '0.2722', '-0.876', '0.521', '0.1744', '0.09204', '-0.2366', '-0.04727', '-0.06744', '0.2727', '-0.09064', '0.0998', '-0.0943', '0.12036', '0.4653', '-0.0874', '-0.35', '-0.0696', '0.1011', '0.1613', '0.2284', '0.7637', '0.2698', '0.151', '-0.02647', '0.4312', '0.02022', '0.5566', '0.2106', '0.4177', '0.657', '-0.1126', '0.3862', '-0.2688', '0.1973', '-0.1045', '0.5635', '0.955']",,,C564484,,,,
mondo:0014197,combined immunodeficiency due to MALT1 deficiency,"['IMD12', 'immunodeficiency 12', 'immunodeficiency type 12']",0111988,615468,397964,C3809583,"['-0.1624', '0.11774', '0.1631', '-0.3254', '0.1437', '-0.3547', '0.3062', '0.02957', '-0.09705', '-0.01955', '-0.0229', '0.1241', '-0.1788', '0.1427', '-0.0719', '-0.1194', '0.1201', '0.1476', '-0.2688', '-0.647', '-0.0921', '-0.213', '0.2435', '-0.3215', '-0.11414', '0.01738', '-0.12427', '-0.003605', '0.0196', '-0.4355', '0.1808', '0.2216', '0.4917', '0.0897', '-0.005863', '-0.0508', '-0.3447', '-0.1833', '-0.1647', '-0.1652', '-0.0609', '-0.1486', '0.2327', '-0.06854', '-0.1686', '-0.1464', '-0.06088', '-0.04608', '0.05695', '0.1635', '-0.1816', '0.02525', '0.399', '0.1339', '-0.198', '-0.10284', '0.00684', '-0.1649', '-0.2705', '-0.01475', '0.10547', '0.2325', '-0.0774', '-0.097', '0.6', '-0.0672', '0.421', '0.1533', '-0.2362', '0.3682', '-0.4697', '-0.11993', '-0.01987', '-0.2223', '-0.01304', '-0.0787', '0.28', '0.04163', '0.2289', '0.1965', '-0.0717', '-0.0963', '-0.1929', '0.09393', '0.0811', '-0.1476', '0.3591', '0.1571', '0.501', '0.02509', '0.3225', '0.2262', '-0.10004', '0.02187', '0.657', '0.469', '0.1677', '-0.1915', '0.03494', '0.1973']",,,,,,,
mondo:0014198,mitochondrial DNA depletion syndrome 13,"['mitochondrial DNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies', 'FBXL4 mitochondrial DNA depletion syndrome', 'encephalomyopathic mitochondrial DNA depletion syndrome-13', 'mitochondrial DNA depletion syndrome 13 (encephalomyopathic type)', 'MTDPS13', 'FBXL4-related encephalomyopathic mitochondrial DNA depletion syndrome', 'BXL4-related early-onset mitochondrial encephalopathy', 'mitochondrial DNA depletion syndrome caused by mutation in FBXL4', 'FBXL4 deficiency', 'mtDNA depletion syndrome, encephalomyopathic form with variable craniofacial anomalies', 'mitochondrial DNA depletion syndrome type 13']",0080131,615471,369897,C3809592,"['-0.4685', '0.409', '0.108', '-0.048', '0.0303', '-0.3918', '-0.1558', '0.3838', '-0.557', '-0.0003164', '-0.0886', '-0.338', '0.0927', '-0.2281', '-0.1037', '0.0253', '-0.2002', '-0.2335', '-0.525', '-0.53', '0.3442', '-0.348', '0.1359', '-0.013725', '0.3176', '-0.03075', '-0.1381', '0.1154', '0.253', '-0.05365', '0.04617', '0.1523', '0.925', '-0.01539', '0.1737', '0.04382', '-0.4507', '-0.2085', '-0.251', '-0.159', '0.1926', '-0.2216', '-0.09827', '0.4646', '-0.3372', '-0.3997', '-0.104', '-0.1453', '0.3838', '-0.1079', '-0.2778', '0.037', '-0.2349', '-0.15', '0.159', '-0.2712', '0.231', '0.3008', '-0.3057', '0.4246', '0.1389', '-0.2096', '0.2583', '-0.117', '-0.1841', '-0.0188', '0.1527', '0.1979', '-0.3853', '0.401', '-0.545', '0.3513', '-0.01201', '0.387', '-0.11865', '0.09937', '0.436', '-0.036', '-0.1045', '0.1553', '0.289', '-0.1986', '-0.1753', '0.3777', '-0.08026', '0.2556', '0.2129', '0.5967', '0.64', '0.56', '0.363', '0.2788', '-0.221', '-0.0639', '0.1857', '0.589', '0.381', '-0.099', '0.4182', '0.2267']",C172095,,,,,,
mondo:0014199,"developmental and epileptic encephalopathy, 17","['early infantile epileptic encephalopathy-17', 'EIEE17', 'epileptic encephalopathy, early infantile, type 17', 'early infantile epileptic encephalopathy caused by mutation in GNAO1', 'GNAO1 early infantile epileptic encephalopathy', 'developmental and epileptic encephalopathy 17', 'GNAO1 encephalopathy', 'DEE17', 'epileptic encephalopathy, early infantile, 17']",0080450,615473,,C3809606,,,,,,,,
mondo:0014200,aldosterone-producing adenoma with seizures and neurological abnormalities,"['aldosterone-secreting adenoma with seizures and neurological abnormalities', 'aldosterone-secreting adenoma', 'Conn adenoma with seizures and neurological abnormalities', 'Conn adenoma', 'primary aldosteronism due to Conn adenoma', 'APA with seizures and neurological abnormalities', 'primary aldosteronism, seizures, and neurologic abnormalities', 'aldosteronoma', 'PASNA']",,615474,85142,C3809609,"['-0.01217', '-0.1658', '-0.08746', '0.08344', '-0.699', '-0.3376', '0.679', '0.08594', '-0.4297', '-0.3376', '-0.3777', '-0.1719', '-0.1469', '0.694', '-0.3757', '0.132', '-0.1368', '-0.12494', '-0.05035', '-0.548', '-0.1365', '0.8613', '0.00889', '-0.1934', '0.2698', '-0.1147', '0.05283', '-0.0903', '-0.3047', '0.6064', '0.0741', '0.07336', '0.586', '0.413', '0.418', '0.4749', '-0.2329', '-0.2042', '0.0806', '-0.438', '-0.2252', '-0.3457', '-0.2252', '-0.456', '0.2078', '-0.2747', '-0.10944', '0.5933', '0.4126', '0.8945', '-0.1649', '0.1886', '0.0898', '-0.706', '-0.007114', '0.3494', '-0.04404', '0.0365', '-0.1088', '0.1396', '-0.1285', '0.3867', '0.57', '-0.1202', '-0.8135', '1.156', '-0.01909', '-0.1619', '-0.838', '0.7065', '0.2625', '0.4795', '-0.0893', '-0.4578', '0.4375', '0.6885', '0.747', '0.4087', '-0.1276', '-0.08813', '-0.07074', '0.93', '0.5957', '0.001052', '0.2472', '-0.1917', '-0.0576', '0.75', '0.643', '1.063', '0.05682', '0.2115', '0.1855', '0.2288', '0.07635', '0.0347', '0.309', '-0.4314', '-0.1016', '0.7466']",,,,,,,
mondo:0014201,"developmental and epileptic encephalopathy, 18","['EIEE18', 'DEE18', 'early infantile epileptic encephalopathy without suppression burst', 'epileptic encephalopathy, early infantile, 18', 'developmental and epileptic encephalopathy 18', 'epileptic encephalopathy, early infantile, type 18']",0080413,615476,369894,C3809624,"['-0.03044', '0.09283', '0.007797', '-0.01686', '0.01245', '-0.1791', '0.1206', '0.1125', '-0.1615', '0.01967', '-0.1771', '-0.093', '0.0367', '-0.003424', '-0.0676', '-0.10785', '-0.0689', '-0.08484', '-0.0518', '-0.258', '-0.0189', '-0.05682', '0.08185', '-0.0788', '0.04544', '-0.02286', '-0.00679', '-0.0749', '-0.11847', '-0.009224', '0.0727', '0.006878', '0.1674', '0.0622', '-0.00796', '0.05606', '-0.0354', '-0.04898', '-0.04437', '-0.09796', '0.02588', '-0.1769', '0.13', '-0.02786', '-0.0508', '-0.0997', '-0.06116', '0.0903', '-0.02678', '0.1497', '-0.0971', '0.03836', '0.07556', '0.01613', '-0.04852', '-0.0487', '0.11017', '-0.1581', '-0.2037', '0.0844', '0.08374', '0.0716', '0.0631', '-0.05453', '-0.00855', '-0.03204', '0.2113', '0.09515', '-0.0825', '0.1427', '-0.1096', '0.0366', '0.02066', '-0.09094', '0.011', '0.0997', '0.04556', '-0.04535', '-0.0684', '-0.0898', '0.01338', '0.05157', '-0.10376', '0.0679', '0.0863', '0.05652', '0.08673', '0.1442', '0.2256', '0.0713', '0.05048', '0.1608', '-0.034', '0.0761', '0.1449', '0.1608', '0.1893', '-0.2642', '0.038', '0.0501']",,,,,,,
mondo:0014202,primary ciliary dyskinesia 24,"['ciliary dyskinesia, primary, 24, without situs inversus', 'CILD24', 'RSPH1 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, type 24', 'primary ciliary dyskinesia type 24', 'primary ciliary dyskinesia 24 without situs inversus', 'primary ciliary dyskinesia caused by mutation in RSPH1', 'ciliary dyskinesia, primary, 24']",0110628,615481,,C3809634,,,,,,,,
mondo:0014203,primary ciliary dyskinesia 25,"['primary ciliary dyskinesia caused by mutation in DNAAF4', 'primary ciliary dyskinesia type 25', 'ciliary dyskinesia, primary, 25, with or without situs inversus', 'CILD25', 'DNAAF4 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 25', 'primary ciliary dyskinesia 25 with or without situs inversus', 'ciliary dyskinesia, primary, type 25']",0110615,615482,,C3809641,,,,,,,,
mondo:0014204,"basal ganglia calcification, idiopathic, 5","['basal ganglia calcification, idiopathic, 5', 'IBGC5', 'basal ganglia calcification, idiopathic, type 5']",,615483,,C3809645,,,,,,,,
mondo:0014205,severe feeding difficulties-failure to thrive-microcephaly due to ASXL3 deficiency syndrome,"['BRPS', 'Bainbridge-Roppers syndrome', 'BAINBRIDGE-ROPERS syndrome']",0080893,615485,352577,C3809650,"['0.3198', '0.02766', '0.1783', '0.1136', '0.1403', '-0.2053', '0.4226', '0.893', '-1.046', '-0.318', '0.1929', '0.09326', '0.5093', '0.4822', '0.2277', '0.01201', '0.556', '0.1877', '-0.6685', '-0.772', '-0.2744', '-0.131', '0.09406', '-0.1896', '0.08527', '0.0985', '0.09247', '0.228', '0.2722', '-0.4402', '-0.07764', '-0.595', '0.2942', '0.08057', '-0.2339', '0.2113', '-0.7437', '-0.2118', '-0.3313', '-0.3484', '-0.02414', '0.1744', '-0.693', '-0.2427', '0.1168', '-0.1053', '0.9546', '0.0402', '-0.2417', '-0.1599', '-0.3496', '-0.7485', '-0.265', '-0.3552', '-0.293', '0.2998', '-0.8867', '0.91', '-0.3586', '0.0771', '0.599', '0.5938', '-0.07074', '0.07074', '0.1061', '-0.3027', '0.8003', '0.1664', '-0.875', '0.1406', '-0.55', '1.025', '0.02751', '-0.4023', '-0.1604', '0.4487', '0.803', '-0.604', '-0.582', '-0.00698', '0.02525', '0.826', '0.2289', '0.382', '0.1621', '0.2874', '0.04974', '-0.2162', '0.8564', '0.6006', '0.3535', '0.2194', '-0.6084', '0.4343', '0.2411', '0.4639', '1.017', '-0.286', '1.142', '-0.7866']",,,,,,,
mondo:0014206,severe early-onset pulmonary alveolar proteinosis due to MARS deficiency,"['infantile liver failure syndrome 2, formerly', 'hereditary pulmonary alveolar proteinosis with hepatic involvement', 'ILLD', 'pulmonary alveolar proteinosis, Reunion island type', 'pulmonary alveolar proteinosis, Reunion Island', 'PAP, Reunion island type', 'infantile liver failure syndrome 2', 'interstitial lung and liver disease']",,615486,440427,C4225400,"['-0.02135', '0.0192', '-0.00816', '-0.00829', '0.005802', '-0.03943', '0.005947', '0.02267', '-0.0328', '-0.01534', '-0.01437', '-0.006996', '-0.008675', '0.01455', '-0.01459', '-0.02824', '0.005085', '0.0004773', '-0.02141', '-0.05392', '0.001605', '-0.01068', '0.02773', '-0.02165', '0.011696', '-0.001799', '-0.01093', '-0.005306', '0.00343', '-0.0253', '0.0322', '0.004105', '0.03702', '0.005318', '0.00985', '-0.00869', '-0.00715', '-0.01421', '-0.00803', '-0.02338', '0.00932', '-0.04007', '0.00695', '-0.00642', '-0.007866', '-0.01888', '-0.01404', '0.02176', '0.006905', '0.011986', '-0.001461', '0.0003877', '0.01339', '0.01017', '-0.02176', '0.00297', '0.02426', '-0.0231', '-0.02791', '0.01', '0.02637', '0.008705', '0.007744', '-0.002573', '0.01211', '-0.0004797', '0.04416', '0.02858', '-0.03073', '0.04047', '-0.03427', '-0.004276', '0.01726', '-0.0277', '0.01052', '0.01308', '0.014435', '-0.0033', '-0.01314', '-0.01657', '-0.00529', '0.003593', '-0.01307', '0.01662', '0.002909', '0.011284', '0.00988', '0.03488', '0.03528', '0.00702', '0.0191', '0.01831', '-0.005497', '0.01773', '0.06616', '0.01097', '0.03207', '-0.04614', '3.666e-05', '0.01999']",,,,,,,
mondo:0014207,age related macular degeneration 14,"['ARMD14', 'macular Degeneration, age-related, type 14', 'age related macular degeneration type 14', 'macular degeneration, age-related, 14, reduced risk of, digenic dominant', 'macular Degeneration, age-related, reduced risk of', 'macular degeneration, age-related, 14']",0110026,615489,,,,,,,,,,
mondo:0014208,Charcot-Marie-Tooth disease type 2R,"['Charcot-Marie-Tooth neuropathy type 2R', 'CMT2R', 'Charcot-Marie-Tooth neuropathy, type 2R', 'TRIM2 Charcot-Marie-Tooth disease type 2', 'autosomal recessive axonal Charcot-Marie-Tooth disease type 2R', 'Charcot-Marie-Tooth disease, type 2R', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2R', 'Charcot-Marie-Tooth disease, axonal, type 2R', 'Charcot-Marie-Tooth disease type 2 caused by mutation in TRIM2']",0110161,615490,397968,C3809655,"['-0.05017', '0.3635', '0.395', '0.02278', '-0.011894', '-0.3755', '0.00994', '0.6855', '-0.749', '0.04565', '-0.11975', '0.3467', '-0.618', '0.3425', '-0.1296', '0.1847', '-0.05777', '-0.4226', '-0.55', '-0.7993', '0.2964', '0.2291', '0.2435', '0.7417', '-0.0411', '0.2668', '0.1249', '0.3323', '-0.12494', '-0.01244', '0.1351', '-0.618', '0.21', '0.0642', '0.402', '-0.718', '-0.695', '-0.4373', '0.549', '-0.1235', '-1.601', '-0.3545', '-0.5015', '0.424', '-0.273', '-0.04327', '0.2898', '-0.0794', '-0.01672', '0.07184', '0.05273', '0.3708', '-0.2268', '-0.969', '-0.0384', '-0.2241', '-0.2284', '0.388', '-0.7153', '-0.142', '-0.3447', '0.02213', '0.8037', '0.682', '-0.899', '1.223', '-0.1361', '0.6963', '-0.6807', '0.38', '-0.6953', '0.0317', '0.3257', '-0.1571', '1.259', '0.3037', '0.03223', '0.4521', '0.165', '-0.5547', '-0.193', '-0.1295', '0.9033', '0.646', '-0.2712', '-0.2544', '0.2402', '0.584', '0.7334', '0.3438', '0.5137', '-0.09296', '0.284', '0.429', '0.4', '0.6787', '0.383', '-0.731', '-0.3247', '0.599']",,,,,,,
mondo:0014209,early-onset progressive neurodegeneration-blindness-ataxia-spasticity syndrome,"['spastic paraplegia 79, autosomal recessive', 'neurodegeneration with optic atrophy, childhood-onset', 'SPG79', 'NDGOA']",0112344,615491,352654,C3809665,"['-0.1357', '-0.271', '0.1492', '-0.04086', '-0.338', '-0.993', '0.002645', '0.0727', '-0.7363', '-0.5205', '0.1815', '0.03516', '-0.2302', '-0.0793', '0.416', '-0.623', '0.2158', '-0.2173', '0.2566', '-1.027', '-0.1649', '-0.2944', '0.0944', '-0.4426', '0.4326', '-0.3345', '-0.4165', '0.3367', '-0.293', '-0.48', '-0.0919', '0.458', '-0.3845', '-0.3433', '0.1974', '0.1024', '-0.1677', '-0.04654', '0.4797', '0.2866', '0.4182', '0.1359', '-0.538', '0.378', '0.4397', '-0.32', '0.1982', '0.2742', '0.375', '-0.1433', '-0.3887', '0.4155', '-0.1733', '-0.4802', '0.09503', '-0.782', '0.4614', '0.3096', '-0.1708', '0.6753', '-0.692', '0.2317', '0.349', '-0.2345', '-0.4177', '0.4958', '0.3613', '0.595', '-0.3835', '0.53', '0.6265', '0.6187', '-0.1594', '-0.7637', '0.7715', '0.0667', '0.257', '0.3987', '0.1037', '0.3225', '-0.1991', '-0.731', '0.532', '0.802', '-0.2637', '-0.4543', '0.2825', '-0.1554', '0.3953', '0.585', '0.3777', '0.4739', '0.0818', '-0.03943', '0.8306', '0.8345', '0.619', '0.3772', '-0.4707', '0.227']",,,,,,,
mondo:0014210,intellectual disability-hypotonia-spasticity-sleep disorder syndrome,"['mental retardation, autosomal recessive 37', 'MRT37', 'intellectual disability, autosomal recessive type 37', 'intellectual disability, autosomal recessive 37', 'mental retardation, autosomal recessive, 37', 'mental retardation, autosomal recessive type 37']",0081202,615493,356996,C3809672,"['-0.1301', '0.258', '0.3298', '-0.589', '-0.1434', '-0.552', '0.1755', '0.4463', '-0.3345', '-0.1411', '-0.2239', '-0.3496', '0.0818', '-0.1569', '0.2081', '0.10974', '0.211', '0.01168', '-0.4536', '-0.587', '0.04062', '-0.04907', '-0.10284', '-0.1538', '0.2115', '-0.189', '0.03558', '-0.086', '0.248', '-0.3486', '0.1727', '0.0354', '0.6553', '0.334', '-0.211', '-0.02428', '-0.1366', '-0.3066', '-0.1019', '-0.4395', '0.4587', '-0.1528', '-0.321', '-0.0732', '0.1857', '-0.4036', '-0.06152', '0.1991', '-0.196', '0.2169', '-0.3486', '0.4563', '-0.2449', '-0.0729', '0.1389', '0.11017', '0.01341', '-0.1199', '-0.1558', '0.1536', '0.0462', '0.07275', '0.1526', '0.002163', '-0.2297', '0.1213', '0.1896', '0.357', '-0.2922', '0.2676', '-0.4077', '0.0944', '-0.0986', '-0.1547', '0.07465', '-0.00333', '0.2167', '-0.0882', '-0.2808', '0.0887', '0.3435', '0.0737', '-0.1998', '0.547', '0.2578', '0.2262', '-0.03354', '0.3354', '0.2386', '0.2947', '0.1522', '0.4934', '-0.09644', '0.10815', '0.459', '0.2103', '0.2206', '-0.198', '0.3928', '0.2761']",,,,,,,
mondo:0014211,primary ciliary dyskinesia 26,"['ciliary dyskinesia, primary, type 26', 'primary ciliary dyskinesia 26 with or without situs inversus', 'primary ciliary dyskinesia type 26', 'ciliary dyskinesia, primary, 26, with or without situs inversus', 'ciliary dyskinesia, primary, 26', 'primary ciliary dyskinesia caused by mutation in CFAP298', 'CFAP298 primary ciliary dyskinesia', 'CILD26']",0110627,615500,,C3809684,,,,,,,,
mondo:0014212,sulfite oxidase deficiency due to molybdenum cofactor deficiency type C,"['MOCODC', 'MOCOD type C', 'molybdenum cofactor deficiency complementation group C', 'molybdenum cofactor deficiency C', 'combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type C', 'molybdenum cofactor deficiency, complementation group type C', 'molybdenum cofactor deficiency, complementation group C', 'molybdenum cofactor deficiency type C']",0111166,615501,308400,C1854990,"['-0.4631', '0.1641', '0.01331', '0.165', '0.307', '-0.395', '-0.2974', '0.03793', '-0.1829', '-0.000781', '-0.111', '-0.02777', '0.1576', '-0.1344', '0.1221', '-0.01982', '-0.1959', '-0.1464', '-0.2422', '-0.424', '0.1573', '-0.2108', '0.2563', '0.0964', '0.0605', '-0.0281', '-0.0637', '0.0325', '0.03467', '-0.2625', '0.2651', '0.3186', '0.1344', '0.0323', '0.1776', '-0.4202', '0.0001609', '-0.1011', '0.0957', '-0.3735', '0.0516', '-0.4724', '0.1321', '-0.02037', '-0.3276', '-0.3223', '0.2152', '0.08386', '0.183', '0.0933', '-0.0564', '-0.315', '-0.069', '0.2874', '-0.24', '-0.2449', '0.509', '-0.05368', '-0.3716', '0.25', '0.03024', '0.1866', '0.2852', '-0.03946', '0.2524', '0.1805', '0.2507', '-0.1133', '-0.333', '0.0958', '-0.2512', '-0.2018', '-0.11115', '-0.11145', '0.2654', '0.3308', '0.005135', '-0.05667', '-0.09125', '0.0649', '0.1863', '0.08215', '-0.1898', '-0.005283', '-0.02873', '-0.0953', '0.1635', '0.5684', '0.4756', '0.0855', '0.03934', '0.1548', '-0.007088', '-0.2869', '0.4746', '0.313', '0.158', '-0.4512', '0.0884', '-0.011635']",,,C565374,,,,
mondo:0014213,intellectual disability-feeding difficulties-developmental delay-microcephaly syndrome,"['mental retardation, autosomal dominant type 21', 'mental retardation, autosomal dominant 21', 'intellectual disability, autosomal dominant 21', 'autosomal dominant mental retardation 21', 'autosomal dominant intellectual disability 21', 'MRD21', 'autosomal dominant non-syndromic intellectual disability 21', 'intellectual disability, autosomal dominant type 21']",0070051,615502,363611,C3809686,"['0.4321', '0.087', '0.1692', '-0.2115', '0.3445', '-0.1602', '0.567', '1.114', '-0.5625', '-0.3298', '-0.05905', '0.131', '0.5986', '0.5713', '0.2242', '-0.1555', '0.3972', '-0.3135', '-0.955', '-0.553', '-0.09894', '0.06915', '-0.0573', '-0.04684', '0.296', '0.0436', '-0.554', '0.25', '0.1982', '-0.2035', '0.05075', '-0.5405', '0.3337', '0.1514', '-0.4043', '0.4485', '-0.817', '-0.2228', '-0.4287', '0.0826', '0.2092', '0.3687', '-0.2356', '-0.749', '0.2903', '-0.1705', '0.487', '-0.2769', '-0.4482', '0.2874', '0.09515', '-0.4895', '-0.2002', '-0.3655', '0.1993', '-0.01903', '-1.055', '0.397', '-0.2003', '0.2053', '0.3796', '0.458', '-0.0825', '0.3557', '-0.06012', '-0.3987', '0.251', '0.1937', '-1.013', '0.1465', '-0.5005', '1.22', '-0.04422', '-0.4514', '0.1038', '0.351', '0.9287', '-0.846', '-0.2666', '-0.1277', '0.01352', '0.6523', '0.3186', '0.5903', '-0.1659', '-0.04462', '-0.02846', '-0.259', '0.7393', '0.7695', '0.1553', '0.475', '-0.1544', '0.2803', '0.1954', '-0.06143', '0.827', '-0.4753', '0.9507', '-0.505']",,,,,,,
mondo:0014214,short-rib thoracic dysplasia 8 with or without polydactyly,"['short rib-polydactyly syndrome, type 6', 'short-rib thoracic dysplasia 8 with or without polydactyly', 'short rib-polydactyly syndrome type VI', 'SRPS6', 'SRTD8']",0110094,615503,,C3809691,,,,,,,,
mondo:0014215,primary ciliary dyskinesia 27,"['ciliary dyskinesia, primary, 27', 'CCDC65 primary ciliary dyskinesia', 'CILD27', 'ciliary dyskinesia, primary, 27, without situs inversus', 'primary ciliary dyskinesia 27 without situs inversus', 'primary ciliary dyskinesia caused by mutation in CCDC65', 'ciliary dyskinesia, primary, type 27', 'primary ciliary dyskinesia type 27']",0110611,615504,,C3809701,,,,,,,,
mondo:0014216,primary ciliary dyskinesia 28,"['ciliary dyskinesia, primary, 28, with or without situs inversus', 'SPAG1 primary ciliary dyskinesia', 'primary ciliary dyskinesia caused by mutation in SPAG1', 'ciliary dyskinesia, primary, 28', 'ciliary dyskinesia, primary, type 28', 'primary ciliary dyskinesia 28 with or without situs inversus', 'CILD28', 'primary ciliary dyskinesia type 28']",0110607,615505,,C3809706,,,,,,,,
mondo:0014217,"telangiectasia, hereditary hemorrhagic, type 5","['telangiectasia, hereditary hemorrhagic, type 5', 'HHT5', 'hereditary hemorrhagic telangiectasia caused by mutation in GDF2', 'GDF2 related HHT-like syndrome', 'GDF2 hereditary hemorrhagic telangiectasia']",,615506,,C3809710,,,,,,,,
mondo:0014218,severe dermatitis-multiple allergies-metabolic wasting syndrome,"['erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper IgE', 'SAM syndrome', 'EPKHE', 'congenital erythroderma-hypotrichosis-recurrent infections-multiple food allergies syndrome', 'severe dermatitis, multiple allergies, and metabolic wasting syndrome', 'Sam syndrome', 'erythroderma, congenital, with palmoplantar keratoderma, hypotrichosis, and hyper-IgE']",,615508,369992,C3809719,"['-0.431', '0.319', '-0.0693', '-0.1021', '-0.1752', '-0.3784', '-0.02255', '-0.3772', '-0.0926', '-0.3938', '0.7886', '0.1848', '0.2157', '0.1128', '-0.888', '0.211', '-0.1802', '-0.07043', '-0.62', '-0.679', '-0.02287', '0.736', '-0.10333', '0.1537', '0.2019', '-0.4075', '-0.03296', '-0.1891', '0.1387', '-0.9727', '0.03253', '0.0827', '0.3655', '-0.2546', '0.2705', '0.393', '-0.3035', '0.1465', '0.1543', '-0.07495', '0.3083', '-0.3228', '-0.417', '-0.2324', '0.1864', '-0.282', '-0.3123', '0.004597', '-0.007515', '-0.1772', '-0.819', '-0.1433', '0.4736', '-0.3545', '-0.6123', '0.172', '-0.4478', '0.34', '-0.7256', '-0.4097', '-0.4624', '0.2086', '-0.377', '-0.1805', '0.1959', '0.4973', '0.8203', '1.065', '0.01066', '0.546', '-0.6323', '0.0887', '-0.563', '-0.1581', '-0.3296', '0.3103', '0.4077', '-0.3335', '0.8223', '0.5425', '0.2343', '0.0689', '-0.5303', '0.1246', '0.3965', '0.0963', '-0.1649', '0.03702', '0.4001', '0.58', '0.3828', '-0.05637', '-0.258', '0.4153', '0.4348', '0.536', '-0.498', '-0.507', '-0.4253', '0.11523']",,,,,,,
mondo:0014219,"alacrima, achalasia, and intellectual disability syndrome","['alacrima, achalasia, and intellectual disability syndrome', 'AAMR', 'GMPPA-CDG', 'alacrima, achalasia, and mental retardation syndrome']",0112321,615510,,C3809738,,,,,,,,
mondo:0014220,myopathy due to myoadenylate deaminase deficiency,"['AMPD1 deficiency', 'AMP deaminase deficiency', 'myopathy due to myoadenylate deaminase deficiency', 'AMP deaminase 1 deficiency', 'MMDD', 'adenosine monophosphate deaminase 1 deficiency', 'myoadenylate deaminase deficiency, myopathy due to', 'myoadenylate deaminase deficiency', 'adenosine monophosphate deaminase-1 deficiency, myopathy due to', 'adenosine monophosphate deaminase deficiency']",,615511,,,,C157504,,,,,,
mondo:0014221,triosephosphate isomerase deficiency,"['TPID', 'hemolytic anemia due to triosephosphate isomerase deficiency', 'hemolytic anaemia due to triosephosphate isomerase deficiency', 'TPI deficiency', 'triose phosphate-isomerase deficiency', 'triosephosphate isomerase deficiency']",0050884,615512,868,C1860808,"['-0.03995', '0.2847', '-0.4238', '0.1265', '0.0717', '-0.314', '-0.01913', '0.8765', '-0.2898', '-0.129', '-0.10223', '0.0707', '-0.0661', '0.03293', '0.4211', '-0.02982', '-0.2678', '-0.1064', '-0.3604', '-0.651', '0.122', '-0.1219', '0.365', '0.1956', '-0.2424', '-0.3577', '-0.4736', '-0.2291', '-0.6924', '-0.1661', '-0.385', '-0.292', '0.2952', '-0.3596', '-0.2769', '-0.3606', '-0.4126', '-0.5825', '0.01782', '-0.2335', '-0.7437', '-0.2196', '0.1582', '0.03973', '0.1685', '-0.0545', '-0.1244', '-0.4443', '0.0923', '-0.3057', '-0.2754', '0.2014', '0.1678', '0.1628', '-0.03214', '0.2167', '0.3323', '-0.2181', '-0.03772', '0.0833', '0.2751', '0.1567', '0.4846', '0.2856', '-0.0754', '-0.3694', '-0.1655', '0.2764', '-0.5483', '0.1434', '-0.05878', '-0.1306', '-0.6733', '0.1334', '0.1442', '-0.1113', '0.2725', '0.3296', '-0.12494', '0.04074', '0.125', '-0.466', '-0.1338', '0.6235', '0.2429', '0.478', '0.5864', '0.4165', '0.5063', '-0.207', '0.2463', '0.1298', '0.338', '-0.4233', '0.6763', '0.602', '0.361', '-0.04105', '0.1761', '-0.2415']",C131652,,C566029,282.3,,,
mondo:0014222,immunodeficiency 14,"['p110-Delta-Activating mutation causing senescent T cells, lymphadenopathy, and immunodeficiency', 'immunodeficiency 14A, autosomal dominant', 'IMD14', 'immunodeficiency type 14', 'immunodeficiency 14', 'Activated PI3K-Delta syndrome']",0111936,615513,,,,,,,,,,
mondo:0014223,amyotrophic lateral sclerosis type 19,"['amyotrophic lateral sclerosis type 19', 'amyotrophic lateral sclerosis caused by mutation in ERBB4', 'ERBB4 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis 19', 'ALS19']",0060210,615515,,C3715155,,,,,,,,
mondo:0014224,developmental delay with autism spectrum disorder and gait instability,"['intellectual disability, autosomal recessive 38', 'mental retardation, autosomal recessive 38', 'intellectual disability, autosomal recessive type 38', 'mental retardation, autosomal recessive type 38', 'developmental delay with ASD and gait instability', 'MRT38', 'intellectual developmental disorder, autosomal recessive 38']",0081203,615516,329195,C3809753,"['0.1307', '0.3289', '0.2416', '0.2715', '-0.0285', '-0.71', '0.484', '0.7744', '-0.4368', '-0.3833', '0.997', '0.2637', '-0.07825', '0.1995', '0.1539', '0.4514', '-0.604', '-0.3132', '-0.3657', '-0.5747', '-0.3167', '-0.3057', '-0.10846', '-0.3303', '0.661', '-0.4526', '0.1832', '-0.02103', '0.00337', '-0.4358', '0.5024', '-0.3735', '1.229', '0.7637', '-0.088', '-0.03738', '-0.3025', '0.4307', '0.5527', '-0.6855', '0.6943', '-0.04434', '-0.9326', '-0.3127', '0.7334', '-1.0625', '0.4727', '-0.327', '-0.154', '0.2234', '-0.642', '-0.1364', '-0.8306', '0.01014', '0.929', '0.122', '-0.5986', '0.3364', '-0.03668', '0.3943', '0.2356', '0.1372', '0.3762', '0.7305', '-0.4346', '-0.1191', '0.5728', '0.172', '-0.4546', '0.3499', '0.55', '0.0805', '-0.3716', '-0.6626', '0.7725', '0.4014', '-0.1109', '0.8433', '-0.1863', '-0.2634', '0.1847', '0.5815', '-0.197', '0.1302', '0.4343', '0.2408', '-0.898', '0.2812', '0.5366', '0.77', '-0.2705', '0.539', '-1.058', '-0.0808', '-0.1709', '0.61', '-0.04807', '-0.4255', '0.295', '-0.01255']",,,,,,,
mondo:0014225,hemochromatosis type 5,"['hemochromatosis, type 5', 'HFE5', 'hereditary hemochromatosis caused by mutation in FTH1', 'FTH1-associated iron overload', 'iron overload, autosomal dominant', 'FTH1 hereditary hemochromatosis', 'FTH1-related iron overload']",0111031,615517,447792,CN237708,"['0.2695', '0.438', '-0.3545', '0.1748', '0.6543', '-0.2167', '-0.752', '0.6255', '0.05496', '-0.0985', '-0.0377', '0.318', '-0.5547', '0.594', '-0.3625', '-0.1642', '-0.4004', '0.1105', '-0.5654', '-0.822', '-0.4995', '-0.5283', '0.3926', '-0.2688', '0.414', '-0.0415', '0.2954', '-0.10455', '0.1489', '0.1942', '0.814', '-0.998', '0.4731', '0.228', '-0.1093', '-0.2861', '-0.8467', '-0.1776', '0.1425', '-0.00824', '0.3555', '-0.1365', '0.007763', '0.667', '0.1669', '-0.964', '-0.04742', '-0.7456', '0.04373', '-0.2269', '0.11523', '0.05093', '0.4753', '0.1844', '0.5947', '-0.2406', '0.425', '0.4314', '-0.1976', '-0.1055', '0.4788', '0.5576', '0.784', '-0.1456', '0.0583', '0.2245', '-0.222', '0.3845', '-0.7725', '-0.3184', '0.2698', '0.2979', '0.2852', '-0.3716', '0.09125', '-0.2922', '0.02539', '0.9395', '-0.1676', '0.509', '0.00918', '-0.396', '-0.3618', '-0.56', '-0.07477', '-0.4802', '0.7964', '0.2474', '0.5957', '0.0821', '1.104', '0.196', '-0.626', '-0.4353', '0.806', '0.812', '-0.2206', '-0.4648', '-0.3186', '0.1273']",,,C565020,,,,
mondo:0014226,idiopathic CD4 lymphocytopenia,"['idiopathic CD4 positive T-lymphocytopenia', 'ICL', 'immunodeficiency 13', 'IMD13', 'idiopathic Cd4 lymphopenia', 'immunodeficiency type 13']",0111987,615518,228000,C3809768,"['-0.02441', '-0.1831', '-0.6235', '-0.671', '-0.0697', '-0.2866', '0.326', '-0.0977', '-0.05777', '0.01662', '0.0745', '0.2128', '-0.2499', '-0.6343', '0.3894', '0.0402', '-0.3142', '0.283', '-0.6', '-0.913', '-0.3132', '-0.1864', '0.94', '-0.6167', '0.1128', '0.05154', '-0.575', '-0.3994', '0.007263', '-0.4758', '0.3308', '-0.2925', '0.545', '0.2266', '0.494', '0.0374', '-0.915', '-0.28', '-0.3696', '0.1381', '0.2268', '0.02617', '0.3374', '-0.2598', '0.2465', '-0.3333', '-0.2289', '-0.1472', '0.1571', '0.2247', '0.3042', '-0.02002', '0.1816', '0.2006', '-0.7314', '0.3843', '-0.0729', '-1.11', '-0.3242', '0.3394', '0.6206', '0.576', '0.2898', '0.526', '0.4028', '0.1315', '0.733', '0.3376', '-0.1504', '0.9067', '-0.1714', '-0.1796', '-0.1921', '-0.296', '0.2434', '-0.2366', '0.3867', '0.2192', '0.4583', '-0.1456', '0.12225', '-0.1576', '0.3762', '0.4202', '-0.3313', '-0.1881', '0.3242', '0.0331', '0.2247', '0.1228', '0.3313', '0.2034', '-0.00221', '-0.2012', '0.6406', '0.7065', '0.3887', '-0.2307', '-0.6416', '-0.179']",,,,,,,
mondo:0014227,hypopigmentation-punctate palmoplantar keratoderma syndrome,"['guttate hypopigmentation and punctate palmoplantar keratoderma', 'guttate hypopigmentation', 'COLED', 'COLE disease', 'hypopigmentation and punctate keratosis of the palms and soles', 'guttate hypopigmentation and punctate palmoplantar keratoderma with or without ectopic calcification', 'punctate palmoplantar keratoderma with or without ectopic calcification', 'Cole disease']",,615522,324561,C3809781,"['-0.1742', '0.2487', '-0.00806', '-0.257', '0.272', '-0.3398', '-0.279', '0.06836', '-0.3162', '0.1251', '-0.1826', '0.02695', '-0.1443', '-0.171', '-0.1881', '0.1032', '0.2756', '-0.3208', '0.05695', '-0.5986', '-0.1483', '-0.0785', '0.359', '-0.0998', '0.063', '0.3762', '-0.2805', '0.086', '0.11743', '-0.1362', '0.1974', '-0.0737', '0.15', '0.05008', '0.2275', '-0.0691', '-0.01675', '-0.0841', '0.09125', '-0.3057', '0.10284', '-0.3079', '-0.0523', '0.03937', '0.1842', '-0.1274', '-0.2678', '0.3079', '0.07355', '-0.001911', '-0.1517', '0.0903', '0.2266', '0.05286', '-0.5073', '-0.10645', '0.3', '-0.06726', '-0.3916', '-0.0999', '0.253', '0.122', '-0.2186', '-0.1023', '0.1137', '-0.01487', '0.3787', '0.402', '0.09705', '0.5806', '-0.451', '-0.1403', '0.2278', '0.06036', '0.0413', '-0.1378', '-0.04382', '0.07623', '-0.05606', '-0.3655', '0.00595', '-0.1309', '0.2642', '0.1263', '-0.01048', '-0.1852', '-0.1732', '0.508', '0.2261', '0.2249', '0.154', '0.1289', '0.2301', '0.0802', '0.4177', '-0.1065', '0.5073', '-0.346', '-0.03026', '0.1136']",,,,757.39,,,
mondo:0014228,"corneal dystrophy, Fuchs endothelial, 8","['Fuchs^ endothelial dystrophy caused by mutation in AGBL1', 'corneal dystrophy, Fuchs endothelial, 8', 'corneal dystrophy, Fuchs endothelial, type 8', 'AGBL1 Fuchs^ endothelial dystrophy', 'FECD8']",,615523,,C3809798,,,,,,,,
mondo:0014229,"microphthalmia, syndromic 12","['MCOPS12', 'syndromic microphthalmia caused by mutation in RARB', 'RARB syndromic microphthalmia', 'microphthalmia, syndromic 12', 'microphthalmia, syndromic type 12', 'syndromic microphthalmia-12', 'microphthalmia with or without pulmonary hypoplasia, diaphragmatic hernia, and/or Cardiac defects']",0111800,615524,,C3809803,,,,,,,,
mondo:0014230,"candidiasis, familial, 8","['TRAF3IP2 chronic mucocutaneous candidiasis (disease)', 'candidiasis, familial, 8', 'candidiasis, familial chronic mucocutaneous, autosomal recessive', 'CANDF8', 'candidiasis, familial, type 8']",,615527,,C3714992,,,,,,,,
mondo:0014231,juvenile onset Parkinson disease 19A,"['DNAJC6 Parkinson disease', 'juvenile onset Parkinson^s disease 19A', 'Parkinson disease 19, juvenile-onset', 'Parkinson disease 19A, juvenile-onset', 'Park19, formerly', 'juvenile onset Parkinson disease type 19A', 'PARK19A', 'PARK19', 'Parkinson disease 19B, early-onset', 'Parkinson disease caused by mutation in DNAJC6']",0060891,615528,,C3809811,,,,,,,,
mondo:0014232,"craniosynostosis 5, susceptibility to","['craniosynostosis 5, susceptibility to', 'ALX4 craniosynostosis', 'susceptibility to craniosynostosis 5', 'CRS5', 'craniosynostosis caused by mutation in ALX4']",,615529,,,,,,,,,,
mondo:0014233,early-onset Parkinson disease 20,"['Parkinson disease 20, early-onset', 'early-onset Parkinson^s disease 20', 'PARK20', 'early-onset Parkinson disease type 20', 'SYNJ1 Parkinson disease', 'Parkinson disease caused by mutation in SYNJ1']",0060898,615530,391411,C3809824,"['-0.07117', '0.5303', '-0.5723', '-0.4922', '-0.4614', '-0.2827', '0.2937', '0.6177', '-0.9097', '0.4316', '-0.0002725', '0.6167', '-0.269', '0.0147', '0.6245', '-0.2172', '0.02852', '-0.5264', '-0.2035', '-0.7573', '-0.0647', '-0.6973', '0.5615', '0.112', '0.1168', '0.4492', '0.1904', '-0.4084', '-0.4146', '-0.359', '0.5215', '0.1445', '0.604', '-0.1605', '-0.05682', '-0.01236', '-0.2607', '-0.11896', '-0.04865', '-0.132', '0.2245', '-0.389', '-0.021', '-0.2272', '1.107', '-0.3186', '-0.1511', '-0.7075', '-0.3823', '0.8755', '0.3838', '0.501', '-0.941', '-0.3809', '-0.303', '0.3606', '0.573', '-0.8735', '-0.184', '-0.183', '0.754', '0.3423', '0.03867', '-0.6895', '-0.342', '0.406', '0.3372', '-0.00049', '0.1996', '0.853', '0.5435', '-0.5913', '-0.001724', '-0.5938', '0.5566', '0.864', '0.3486', '0.1608', '-0.7993', '-0.642', '0.3225', '-0.4463', '0.5737', '0.931', '0.1625', '0.1423', '-0.4468', '-0.5835', '0.9473', '0.0908', '0.1624', '-0.09534', '-0.04767', '1.008', '0.511', '0.3997', '0.605', '0.862', '-0.5146', '-0.4634']",,,,,,,
mondo:0014234,reticulate acropigmentation of Kitamura,"['reticulate acropigmentation of Kitamura', 'RAPK', 'Kitamura reticulate acropigmentation', 'RAK', 'reticulate pigmentation of Kitamura', 'acropigmentatio reticularis']",0060258,615537,178307,,"['-0.4285', '0.2467', '-0.04755', '-0.312', '0.292', '-0.3281', '-0.229', '-0.10974', '-0.4788', '-0.1138', '0.01124', '0.01692', '-0.3887', '-0.00822', '-0.1888', '0.1641', '0.465', '-0.534', '0.2245', '-0.5938', '-0.1118', '-0.03207', '0.4229', '-0.08875', '0.09674', '0.3325', '0.010284', '0.1573', '-0.2207', '0.005234', '0.4368', '-0.3577', '-0.0274', '0.01538', '0.3079', '0.10596', '-0.4019', '-0.143', '0.249', '-0.4355', '-0.1943', '-0.2181', '-0.01437', '-0.06854', '-0.214', '-0.3523', '-0.41', '0.2035', '-0.0799', '-0.12476', '-0.3865', '0.0343', '0.1045', '0.2976', '-0.546', '-0.04846', '0.4714', '0.003145', '-0.3477', '0.001947', '-0.1995', '-0.0931', '-0.245', '0.2017', '-0.2878', '0.1339', '0.555', '0.616', '0.2245', '0.555', '-0.2432', '0.057', '0.3718', '0.1617', '-0.06323', '-0.1344', '-0.125', '-0.12213', '0.11597', '-0.604', '-0.1431', '-0.4304', '0.5024', '0.2542', '0.2189', '-0.2747', '-0.3708', '0.4382', '0.2825', '0.3633', '0.2473', '0.1412', '-0.05225', '0.3408', '0.2522', '-0.2013', '0.2583', '-0.3323', '0.2654', '0.4658']",,,C562924,709.09,,,
mondo:0014235,chromosome 22q13 duplication syndrome,"['chromosome 22q13 duplication syndrome', 'chromosome 22q13 duplication syndrome, isolated cases']",0060437,615538,,C3809844,,,,,,,,
mondo:0014236,"Ehlers-Danlos syndrome, musculocontractural type 2","['Ehlers-Danlos syndrome, musculocontractural type caused by mutation in DSE', 'EDSMC2', 'Ehlers-Danlos syndrome, musculocontractural type, 2', 'Ehlers-Danlos syndrome, musculocontractural type 2', 'DSE Ehlers-Danlos syndrome, musculocontractural type']",0080737,615539,,C3809845,,,,,,,,
mondo:0014237,autosomal recessive nonsyndromic hearing loss 76,"['DFNB76', 'autosomal recessive nonsyndromic deafness caused by mutation in SYNE4', 'deafness, autosomal recessive type 76', 'autosomal recessive nonsyndromic deafness 76', 'deafness, autosomal recessive 76', 'SYNE4 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 76', 'autosomal recessive deafness 76']",0110524,615540,,C3147083,,,,,,,,
mondo:0014238,severe intellectual disability-short stature-behavioral abnormalities-facial dysmorphism syndrome,"['mental retardation, autosomal recessive type 39', 'intellectual disability, autosomal recessive 39', 'MRT39', 'mental retardation, autosomal recessive 39', 'intellectual disability, autosomal recessive type 39']",0081204,615541,391307,C3809853,"['-0.2119', '0.06805', '0.4883', '-0.4543', '-0.04214', '-0.2588', '0.1575', '0.527', '-0.5825', '-0.03958', '-0.03708', '-0.06036', '0.1527', '-0.05624', '-0.1071', '0.1334', '0.434', '-0.01616', '-0.163', '-0.618', '-0.01846', '0.08405', '-0.00817', '-0.04083', '0.2179', '-0.1793', '-0.2534', '-0.164', '0.3381', '-0.3323', '0.1638', '-0.0933', '0.3926', '0.2595', '0.11206', '-0.1785', '-0.1399', '-0.379', '-0.2003', '-0.4727', '0.313', '-0.1581', '-0.2659', '-0.0532', '-0.00402', '-0.304', '0.005623', '0.3335', '-0.1108', '0.1726', '-0.313', '0.0815', '-0.11615', '0.10175', '-0.1661', '-0.1667', '-0.1763', '-0.1599', '0.01125', '0.191', '-0.064', '0.06793', '-0.2454', '0.236', '-0.03293', '-0.0677', '0.1356', '0.3826', '-0.11053', '0.354', '-0.4558', '0.2045', '0.11304', '-0.2737', '-0.2346', '0.05954', '0.2544', '-0.384', '-0.252', '0.02411', '0.06186', '-0.2534', '-0.1898', '0.6904', '-0.057', '0.291', '-0.156', '0.2722', '0.3704', '0.334', '-0.01976', '0.5317', '0.1658', '0.1389', '0.584', '0.1294', '0.2172', '-0.325', '0.5864', '0.2164']",,,,,,,
mondo:0014239,testicular anomalies with or without congenital heart disease,"['TACHD', 'testicular anomalies with or without congenital heart disease']",,615542,,C3809858,,,,,,,,
mondo:0014240,periventricular nodular heterotopia 6,"['periventricular nodular heterotopia type 6', 'periventricular nodular heterotopia caused by mutation in ERMARD', 'PVNH6', 'ERMARD periventricular nodular heterotopia', 'periventricular nodular heterotopia 6']",,615544,,C3809872,,,,,,,,
mondo:0014241,"leukemia, acute lymphoblastic, susceptibility to, 3","['PAX5 precursor B-cell acute lymphoblastic leukaemia', 'susceptibility to acute lymphoblastic leukemia 3', 'ALL3', 'precursor B-cell acute lymphoblastic leukemia caused by mutation in PAX5', 'susceptibility to acute lymphoblastic leukaemia 3', 'leukemia, acute lymphoblastic, susceptibility to, type 3', 'precursor B-cell acute lymphoblastic leukaemia caused by mutation in PAX5', 'leukemia, acute lymphoblastic, susceptibility to, 3', 'PAX5 precursor B-cell acute lymphoblastic leukemia']",,615545,,C3809874,,,,,,,,
mondo:0014242,van Maldergem syndrome 2,"['van Maldergem syndrome 2', 'van Maldergem syndrome caused by mutation in FAT4', 'FAT4 van Maldergem syndrome', 'Van Maldergem syndrome type 2', 'VMLDS2', 'VAN Maldergem syndrome 2']",0080586,615546,,C3809875,,,,,,,,
mondo:0014243,Schaaf-Yang syndrome,"['distal arthrogryposis with hypopituitarism, intellectual disability and facial anomalies', 'Prader-Willi-like syndrome', 'arthrogryposis, distal, with hypopituitarism, intellectual disability, and facial anomalies', 'Schaaf-Yang syndrome', 'SHFYNG', 'Chitayat-Hall syndrome', 'PWS due to a point mutation', 'MAGEL2-related PWLS', 'arthrogryposis, distal, with hypopituitarism, mental retardation, and facial anomalies', 'MAGEL2-related Prader-Willi-like syndrome', 'Prader-Willi syndrome due to point mutation']",0111715,615547,398069,C3809877,"['-0.2778', '0.11', '0.00874', '0.2045', '0.05746', '-0.2461', '-0.643', '0.8257', '-0.3767', '-0.2703', '-0.3042', '-0.678', '0.2357', '0.7256', '-0.04333', '-0.2455', '-0.04883', '0.6055', '-1.004', '-0.3027', '-0.173', '0.1719', '0.366', '-0.264', '0.4534', '0.008995', '-0.0319', '-0.2311', '0.3403', '-0.2659', '0.715', '-0.4084', '0.01459', '0.427', '-0.4985', '0.2896', '0.05283', '0.1594', '0.07526', '-0.526', '1.002', '0.6377', '-0.59', '-0.02585', '-0.1016', '-0.596', '0.661', '0.2135', '0.4426', '0.4478', '-0.5024', '0.04697', '-0.7393', '0.08484', '0.02849', '-0.08795', '-0.04108', '0.686', '0.3977', '-0.10046', '-0.10895', '0.6772', '0.0997', '-0.3638', '-0.765', '0.3848', '-0.3005', '0.06525', '-0.528', '0.5864', '0.0396', '-0.1641', '-0.1573', '-0.4548', '0.0222', '0.0995', '-0.01593', '0.6265', '-0.03757', '-0.08496', '0.1703', '0.394', '-0.0885', '-0.0711', '0.239', '0.06146', '0.05667', '-0.3308', '1.082', '0.4458', '0.03925', '0.0874', '-0.7437', '0.26', '0.693', '-0.05286', '-0.1875', '-0.8325', '0.02945', '0.437']",,,C535385,,,,
mondo:0014244,hereditary sensory and autonomic neuropathy type 7,"['SCN11A autosomal dominant hereditary sensory and autonomic neuropathy', 'HSAN 7', 'neuropathy, hereditary sensory and autonomic, type VII', 'CIP with hyperhidrosis and gastrointestinal dysfunction', 'insensitivity to pain, congenital, with gastrointestinal dysfunction and hyperhidrosis', 'HSAN with hyperhidrosis and gastrointestinal dysfunction', 'hereditary sensory and autonomic neuropathy with hyperhidrosis and gastrointestinal dysfunction', 'congenital insensitivity to pain with hyperhidrosis and gastrointestinal dysfunction', 'hereditary sensory and autonomic neuropathy type VII', 'HSAN VII', 'neuropathy, hereditary sensory and autonomic, type 7', 'HSAN7', 'autosomal dominant hereditary sensory and autonomic neuropathy caused by mutation in SCN11A']",0070149,615548,391397,C3809882,"['0.7026', '-0.2727', '-0.17', '0.28', '-0.109', '-0.4875', '-0.2073', '0.449', '-0.733', '0.206', '0.000662', '0.6626', '0.1952', '0.4995', '-0.622', '0.514', '0.2018', '0.5117', '-0.627', '-0.8887', '0.4631', '0.05', '-0.797', '0.437', '0.00826', '-0.2698', '-0.543', '-0.0249', '-0.0389', '-0.2993', '0.772', '-0.02296', '0.0959', '0.02472', '-0.5024', '-0.2078', '0.0635', '0.02625', '0.02121', '-0.06805', '-0.5747', '-0.1835', '-0.3752', '-0.1471', '0.1037', '-0.0573', '0.3655', '0.02054', '0.471', '0.3586', '-0.7837', '0.7676', '0.2576', '-0.56', '-0.0823', '0.501', '0.2205', '0.12476', '-0.3086', '-0.2637', '0.6416', '0.495', '0.519', '0.0751', '0.1847', '0.5747', '0.1396', '0.8564', '0.2089', '0.5127', '-0.863', '0.1082', '-0.515', '-0.4421', '0.8237', '-0.346', '0.00647', '0.829', '-0.429', '0.374', '-0.0546', '-0.863', '0.4343', '0.08997', '-0.3235', '-0.13', '0.615', '-0.01787', '0.66', '-0.2168', '0.134', '0.1609', '0.1263', '-0.253', '0.7295', '0.8745', '-0.06323', '-0.2651', '0.7095', '0.05695']",C125388,,,,,,
mondo:0014245,Diamond-Blackfan anemia 12,"['Diamond-Blackfan anemia caused by mutation in RPL15', 'Diamond-Blackfan Anemia type 12', 'DBA12', 'RPL15 Diamond-Blackfan anemia', 'Diamond-Blackfan anemia 12', 'Diamond-Blackfan Anaemia type 12', 'RPL15 Diamond-Blackfan anaemia', 'Diamond-Blackfan anaemia caused by mutation in RPL15']",0111882,615550,,C3809888,,,,,,,,
mondo:0014246,"episodic pain syndrome, familial, 2","['episodic pain syndrome, familial, type 2', 'FEPS2', 'episodic pain syndrome, familial, 2', 'SCN10A familial episodic pain syndrome', 'familial episodic pain syndrome caused by mutation in SCN10A']",0111730,615551,,C3809893,,,,,,,,
mondo:0014247,familial episodic pain syndrome with predominantly lower limb involvement,"['episodic pain syndrome, familial, 3', 'episodic pain syndrome, familial, type 3', 'FEPS3']",0111731,615552,391392,C3809899,"['-0.2161', '-0.07825', '-0.3928', '-0.2178', '0.0695', '-0.5327', '0.1257', '0.5', '-0.4106', '-0.12494', '0.002272', '0.3489', '-0.1233', '0.371', '0.204', '0.133', '-0.01758', '-0.2273', '0.01994', '-0.4048', '0.0637', '-0.2896', '0.001695', '-0.1959', '-0.127', '0.2805', '0.09796', '-0.09607', '-0.2301', '-0.307', '0.03812', '0.1844', '-0.1755', '0.0556', '-0.04904', '0.06155', '-0.2317', '-0.2056', '0.2153', '0.1095', '0.0576', '-0.594', '0.1927', '0.4795', '0.4875', '-0.008316', '-0.77', '0.349', '0.429', '0.347', '-0.542', '0.2365', '0.02565', '0.2144', '0.1516', '-0.0379', '0.4153', '-0.02803', '-0.4036', '-0.508', '0.0656', '0.483', '0.003801', '-0.4573', '0.01021', '0.1526', '0.4053', '0.2961', '0.3071', '0.3303', '-0.5435', '-0.03043', '0.2578', '0.1621', '0.4773', '0.6743', '0.1062', '0.4187', '0.368', '-0.3452', '-0.2351', '-0.04398', '0.681', '0.04092', '0.265', '-0.07086', '-0.00888', '0.579', '0.4502', '0.03928', '0.2155', '-0.05106', '0.411', '0.07043', '0.521', '0.00578', '0.679', '-0.5103', '-0.446', '0.1746']",C125390,,,,,,
mondo:0014248,autism spectrum disorder - epilepsy - arthrogryposis syndrome,"['AMRS', 'arthrogryposis, mental retardation, and seizures', 'arthrogryposis, intellectual disability, and seizures', 'SLC35A3-CDG', 'arthrogryposis, impaired intellectual development, and seizures']",,615553,370943,C3809910,"['0.2917', '0.3264', '0.1948', '0.09705', '0.1641', '-0.647', '0.5073', '0.8657', '-0.5103', '-0.5093', '0.949', '0.2776', '-0.0598', '0.2634', '0.2236', '0.4043', '-0.3875', '-0.1641', '-0.3762', '-0.4976', '-0.4216', '-0.3408', '0.0729', '-0.2396', '0.608', '-0.2903', '0.2908', '0.1765', '0.2122', '-0.3074', '0.5483', '-0.4783', '1.174', '0.534', '-0.1542', '-0.0843', '-0.2399', '0.372', '0.3367', '-0.544', '0.6753', '-0.3013', '-0.9185', '-0.2664', '0.6694', '-0.963', '0.3835', '-0.1914', '-0.03204', '0.0863', '-0.7056', '-0.178', '-0.813', '-0.0681', '0.8833', '0.00407', '-0.795', '0.277', '-0.14', '0.3984', '0.0317', '-0.03354', '0.2534', '0.7236', '-0.6', '-0.11505', '0.429', '0.1292', '-0.4573', '0.271', '0.4673', '-0.1283', '-0.3086', '-0.409', '0.799', '0.3723', '-0.03032', '0.7515', '-0.2551', '-0.2515', '0.11127', '0.3152', '-0.1453', '0.1921', '0.4202', '0.1417', '-0.599', '0.1971', '0.405', '0.7144', '-0.1515', '0.431', '-0.817', '0.0771', '-0.3403', '0.483', '0.1598', '-0.4312', '0.5776', '-0.2147']",,,,,,,
mondo:0014249,multiple fibroadenoma of the breast,"['mammary polyadenomatosis', 'MFAB', 'multiple fibroadenomas of the breast']",,615554,50920,C3809918,,,,,,,,
mondo:0014250,familial hyperprolactinemia,"['familial isolated prolactin receptor deficiency', 'hyperprolactinemia', 'familial hyperprolactinemia', 'hereditary hyperprolactinemia (disease)', 'HPRL']",,615555,397685,C0020514,"['-0.359', '-0.1593', '-0.559', '-0.3005', '-0.321', '0.01485', '-0.515', '0.2827', '-0.269', '-0.276', '-0.03418', '0.1012', '-0.1599', '0.3804', '0.1592', '-0.3074', '0.1764', '0.2438', '-0.3027', '-0.7827', '-0.2443', '-0.4854', '0.4392', '-0.3745', '0.1586', '0.0919', '0.0911', '-0.541', '-0.02853', '-1.043', '1.074', '-0.4258', '0.859', '0.02464', '0.10187', '-0.2908', '-0.4146', '-0.1708', '-0.4167', '-0.1228', '0.8022', '0.3074', '0.3584', '-0.5293', '0.3135', '-0.3838', '0.06525', '0.1071', '-0.3193', '0.4329', '-0.0695', '-0.1227', '-0.4219', '0.1366', '-0.2152', '0.2517', '0.3936', '-0.536', '-0.232', '0.3235', '0.3765', '0.466', '0.2336', '-0.536', '-0.3245', '0.4495', '0.2742', '0.688', '-0.6704', '0.1681', '-0.3225', '0.416', '-0.3726', '-0.04254', '0.4626', '-0.08795', '-0.6396', '0.1339', '-0.02196', '-0.08795', '0.3557', '0.7773', '0.578', '0.0754', '0.1464', '-0.1455', '0.1782', '-0.8545', '0.539', '-0.3972', '-0.2349', '0.435', '0.04712', '-0.3213', '0.9683', '0.3428', '0.01749', '-0.1503', '-0.3406', '-0.2092']",,,,,E22.1,,
mondo:0014251,"melioidosis, susceptibility to","['melioidosis, susceptibility to', 'melioidosis, resistance to', 'susceptibility to melioidosis']",,615557,,,,,,,,,,
mondo:0014252,familial hypobetalipoproteinemia 1,"['FHBL', 'familial hypobetalipoproteinemia type 1', 'hypobetalipoproteinemia, familial', 'hypobetalipoproteinemia, familial, 1', 'hypobetalipoproteinemia, familial, type 1', 'acanthocytosis with hypobetalipoproteinemia', 'hypobetalipoproteinemia, Normotriglyceridemic', 'FHBL1', 'APOB hypobetalipoproteinemia', 'hypobetalipoproteinemia caused by mutation in APOB', 'hypobetalipoproteinemia']",0111062,615558,,CN182502,,,,C566267,,,,
mondo:0014254,otofaciocervical syndrome 2,"['PAX1 otofaciocervical syndrome', 'otofaciocervical syndrome caused by mutation in PAX1', 'otofaciocervical syndrome 2', 'OFC2', 'otofaciocervical syndrome type 2', 'OTFCS2']",,615560,,C3714942,,,,,,,,
mondo:0014255,complement factor b deficiency,"['complement factor B deficiency', 'complement factor b deficiency', 'CFBD']",,615561,,C3809950,,,,,,,,
mondo:0014256,retinitis pigmentosa 67,"['NEK2 retinitis pigmentosa', 'retinitis pigmentosa type 67', 'RP67', 'retinitis pigmentosa 67', 'retinitis pigmentosa caused by mutation in NEK2']",0110359,615565,,C3809954,,,,,,H35.5,,
mondo:0014257,"nephrotic syndrome, type 9","['COQ8B nephrotic syndrome', 'nephrotic syndrome caused by mutation in COQ8B', 'NPHS9', 'nephrotic syndrome, type 9']",0080391,615573,,C3809965,,,,,,,,
mondo:0014258,congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome,"['ASNSD', 'asparagine synthetase deficiency', 'Asns deficiency']",,615574,391376,C3809971,"['-0.1278', '0.264', '0.523', '-0.1047', '0.3596', '-0.0652', '0.2566', '0.681', '-1.254', '-0.299', '0.08325', '-0.02144', '0.4973', '0.199', '0.5127', '-0.293', '0.828', '0.2286', '-0.4644', '-0.984', '-0.03125', '0.01787', '-0.1226', '0.165', '0.4075', '0.363', '0.05515', '0.1891', '0.191', '-0.345', '-0.226', '-0.0805', '0.697', '-0.08563', '-0.3394', '1.034', '-0.585', '-0.26', '0.113', '-0.1838', '0.08984', '-0.0564', '-0.903', '-0.1245', '0.1125', '-0.6323', '0.7905', '0.1266', '-0.1548', '0.01298', '0.0891', '-0.4587', '-0.1204', '-0.614', '0.06946', '0.07684', '-0.564', '0.568', '-0.589', '0.4492', '0.1361', '0.4272', '0.711', '0.1763', '-0.2405', '-0.1371', '0.5747', '0.2258', '-0.9253', '0.0993', '-0.769', '1.063', '0.07886', '-0.625', '0.0795', '0.347', '0.623', '-0.1372', '-0.2379', '0.09503', '-0.3208', '1.107', '0.4226', '0.5215', '0.002808', '-0.1558', '0.1146', '-0.571', '0.93', '0.3503', '0.1855', '0.07904', '-0.3567', '0.2512', '-0.3923', '0.462', '1.225', '-0.3481', '0.8193', '-0.59']",,,,,,,
mondo:0014259,"neuronopathy, distal hereditary motor, type 2D","['neuronopathy, distal hereditary motor, type IID', 'neuropathy, distal hereditary motor, type 2D', 'HMN 2D', 'neuronopathy, distal hereditary motor caused by mutation in FBXO38', 'HMN2D', 'spinal muscular atrophy, distal, autosomal dominant, calf-predominant', 'FBXO38 neuronopathy, distal hereditary motor']",0111210,615575,,,,,,,,,,
mondo:0014260,"immunodeficiency, common variable, 10","['CVID10', 'NFKB2 common variable immunodeficiency', 'Deficit in anterior pituitary function and variable immunodeficiency', 'immunodeficiency, common variable, with central adrenal insufficiency', 'common variable immunodeficiency caused by mutation in NFKB2', 'immunodeficiency, common variable, 10', 'immunodeficiency, common variable, type 10']",0081152,615577,,C3809991,"['-0.0481', '0.10205', '0.01677', '-0.04626', '0.03818', '-0.0692', '0.02461', '0.1315', '-0.1034', '-0.0758', '-0.02295', '0.01102', '-0.0039', '0.02681', '-0.0636', '-0.04733', '0.01813', '-0.06097', '-0.02498', '-0.1641', '-0.03613', '-0.0724', '0.10846', '-0.03986', '0.04907', '-0.0305', '-0.03802', '-0.010315', '0.01465', '-0.0632', '0.08826', '-0.0084', '0.09485', '0.0704', '-0.001646', '-0.04163', '-0.11597', '-0.0391', '-0.03592', '-0.0525', '0.03625', '-0.0955', '0.02567', '-0.04752', '-0.01251', '-0.0837', '-0.03696', '0.0402', '0.02863', '0.0323', '0.001742', '-0.05054', '0.01476', '0.004063', '-0.06915', '-0.03308', '0.0962', '-0.0799', '-0.09607', '-0.02576', '0.05026', '0.07324', '-0.004005', '0.03087', '0.0397', '-0.01732', '0.0885', '0.10406', '-0.0863', '0.1164', '-0.07007', '0.03418', '0.01845', '-0.0761', '0.06323', '0.074', '0.0391', '-0.001762', '-0.02618', '-0.0642', '0.02782', '-0.01979', '-0.04303', '0.072', '0.006054', '0.0437', '0.05972', '0.10693', '0.1289', '0.002838', '0.05743', '0.1183', '-0.02574', '0.01559', '0.2358', '0.10565', '0.0762', '-0.1566', '0.00894', '0.02469']",,,,,,,
mondo:0014261,growth and developmental delay-hypotonia-vision impairment-lactic acidosis syndrome,"['COXPD18', 'combined oxidative phosphorylation deficiency caused by mutation in SFXN4', 'combined oxidative phosphorylation deficiency type 18', 'SFXN4 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 18']",0111484,615578,391348,C3810001,"['-0.7515', '0.1554', '0.2979', '-0.2805', '-0.0691', '-0.4436', '0.01793', '0.5894', '-0.4602', '-0.04922', '-0.2229', '-0.10394', '0.0781', '-0.1978', '0.2385', '-0.09796', '0.247', '-0.1683', '-0.321', '-0.6826', '0.216', '-0.1995', '0.1125', '0.246', '0.2357', '-0.1384', '0.125', '-0.05573', '-0.185', '-0.15', '0.02066', '0.381', '0.6895', '0.1917', '-0.1917', '-0.2087', '0.0315', '-0.137', '-0.1487', '-0.1306', '0.1467', '-0.0672', '-0.11194', '0.3928', '-0.3052', '-0.4722', '0.04807', '0.2059', '0.0316', '-0.0426', '-0.376', '-0.0942', '-0.01216', '-0.0948', '-0.03152', '-0.184', '0.2085', '0.0426', '-0.1186', '0.394', '-0.06964', '-0.1327', '0.4133', '-0.00953', '-0.1006', '0.10657', '0.141', '0.2893', '-0.2115', '0.101', '-0.2334', '0.004627', '-0.03888', '-0.2191', '0.1693', '-0.1958', '0.3542', '-0.1915', '-0.0728', '0.4592', '0.1361', '-0.10864', '-0.1978', '0.2355', '0.05368', '-0.03726', '0.1139', '0.3655', '0.6475', '0.4229', '0.4355', '0.313', '0.1271', '-0.1263', '0.72', '0.5586', '0.12146', '-0.0964', '0.2842', '0.1937']",,,,,,,
mondo:0014262,Rienhoff syndrome,"['LDS5', 'Loeys-Dietz syndrome 5', 'Rienhoff syndrome', 'Loeys-Dietz syndrome type 5']",0070236,615582,,C3810012,"['-0.1637', '0.03928', '-0.0744', '-0.2294', '0.2297', '-0.4575', '0.2864', '0.2534', '-0.1201', '-0.231', '-0.078', '-0.2118', '0.1487', '0.3076', '-0.244', '0.004765', '-0.2063', '-0.1558', '-0.2712', '-0.3848', '0.3315', '0.1595', '0.3972', '0.0794', '0.1731', '0.2554', '0.369', '0.1923', '0.4', '0.00772', '0.3904', '-0.238', '0.2712', '0.2698', '0.332', '-0.1786', '0.03995', '-0.02055', '0.0217', '-0.534', '0.1582', '-0.0382', '0.3203', '-0.1913', '0.3647', '-0.0395', '0.03064', '0.4236', '-0.2563', '0.178', '-0.0921', '-0.0661', '0.04605', '0.1626', '-0.2551', '-0.2605', '0.1669', '-0.1902', '-0.0975', '0.006783', '0.4124', '-0.0564', '-0.2656', '-0.1854', '0.0175', '0.03998', '0.2389', '0.414', '0.01119', '0.5596', '-0.4705', '-0.1509', '0.1049', '-0.1637', '-0.1014', '0.05728', '0.11633', '-0.229', '-0.4617', '-0.3323', '-0.1824', '-0.01836', '0.0135', '0.2429', '-0.01743', '-0.06216', '0.2045', '-0.07184', '-0.02867', '-0.2014', '0.06018', '-0.227', '-0.0398', '0.1609', '0.522', '-0.2397', '0.514', '-0.02756', '-0.02399', '-0.1473']",,1000012,,,,,
mondo:0014263,8q24.3 microdeletion syndrome,"['VRJS', 'chromosome 8Q24.3 deletion syndrome', 'Verheij syndrome']",,615583,508488,C3810023,"['-0.004883', '0.05093', '0.0193', '-0.01968', '0.01598', '-0.04727', '0.0175', '0.0453', '-0.03372', '-0.01183', '-0.02794', '-0.00822', '0.00723', '-0.001662', '-0.002022', '-0.01872', '-0.003426', '-0.00795', '-0.02707', '-0.06195', '0.004303', '0.001474', '0.0477', '-0.03021', '0.01566', '-0.01486', '-0.01314', '-0.006645', '0.02028', '-0.02333', '0.02374', '-0.01142', '0.0542', '0.0246', '0.01119', '-0.01491', '-0.007744', '-0.02325', '-0.01208', '-0.03464', '0.001562', '-0.03029', '0.001963', '-0.0312', '0.002645', '-0.03986', '-0.01513', '0.03293', '0.0169', '0.007023', '-0.02827', '-0.01162', '-0.01077', '0.00735', '-0.02684', '-0.009735', '0.02441', '-0.01472', '-0.03738', '0.01936', '0.02176', '0.01285', '0.008255', '0.01265', '0.01166', '-0.01354', '0.0345', '0.02573', '-0.04306', '0.04724', '-0.04755', '0.001844', '0.01261', '-0.01967', '0.01695', '0.01778', '7.46e-05', '-0.00488', '-0.02873', '-0.01342', '-0.004566', '0.0004745', '-0.02135', '0.05203', '-0.01382', '0.00415', '0.01386', '0.05493', '0.04007', '0.00277', '0.014084', '0.03357', '0.0001495', '0.01846', '0.0764', '0.00858', '0.03842', '-0.0584', '-0.0005155', '0.0077']",,,,,,,
mondo:0014264,otosclerosis 10,"['otosclerosis 10', 'OTSC10']",,615589,,,,,,,,,,
mondo:0014265,Alzheimer disease 18,"['Alzheimer disease type 18', 'ADAM10 Alzheimer disease', 'Alzheimer^s disease 18', 'Alzheimer disease caused by mutation in ADAM10', 'AD18', 'Alzheimer^s disease type 18', 'Alzheimer disease 18, late-onset', 'Alzheimer disease 18, susceptibility to', 'Alzheimer disease 18']",0110050,615590,,C3810041,,,,,,,,
mondo:0014266,age related macular degeneration 15,"['macular degeneration, age-related, type 15', 'macular degeneration, age-related, 15, susceptibility to', 'C9 age-related macular degeneration', 'ARMD15', 'age-related macular degeneration caused by mutation in C9', 'age related macular degeneration type 15', 'macular degeneration, age-related, 15']",0110027,615591,,C3810042,,,,,,,,
mondo:0014267,severe combined immunodeficiency due to IKK2 deficiency,"['immunodeficiency 15', 'IMD15', 'immunodeficiency type 15', 'SCID due to IKK2 deficiency', 'immunodeficiency 15B']",0111959,615592,397787,C3810043,"['-0.1895', '0.2316', '0.1094', '-0.2034', '0.132', '-0.2678', '0.1523', '0.1401', '-0.1053', '-0.2002', '-0.0818', '0.05438', '-0.298', '0.08405', '-0.00628', '-0.1487', '0.09576', '0.2239', '-0.2651', '-0.594', '-0.1353', '-0.2443', '0.4731', '-0.06824', '0.1115', '-0.0869', '-0.1383', '-0.01973', '-0.1617', '-0.463', '0.1382', '0.4336', '0.43', '0.03314', '-0.03802', '-0.0304', '-0.3606', '0.008766', '-0.3567', '-0.3115', '-0.2104', '-0.1901', '0.08264', '-0.05875', '-0.549', '-0.2068', '-0.2617', '-0.1866', '0.1997', '0.2096', '0.0626', '-0.2307', '0.3303', '-0.1451', '-0.2402', '0.04413', '0.1072', '-0.39', '-0.1469', '0.2219', '-0.010414', '0.2795', '0.04602', '0.005142', '0.4514', '-0.07275', '0.3025', '0.3455', '-0.3777', '0.288', '-0.276', '-0.068', '0.06244', '-0.2188', '0.2002', '-0.1407', '0.267', '0.1221', '0.1182', '0.1141', '-0.1821', '-0.03638', '-0.169', '0.0818', '0.1038', '-0.05322', '0.239', '0.0617', '0.5137', '0.05463', '0.4043', '0.4368', '-0.157', '-0.0444', '0.5244', '0.659', '0.2083', '-0.5137', '-0.0697', '0.12476']",,,,,,,
mondo:0014268,combined immunodeficiency due to OX40 deficiency,"['OX40 deficiency', 'combined immunodeficiency with impaired immunity to HHV-8', 'immunodeficiency 16', 'immunodeficiency type 16', 'IMD16', 'combined immunodeficiency with impaired immunity to human herpes virus 8', 'combined immunodeficiency with childhood-onset Kaposi sarcoma']",0111935,615593,431149,C3810053,,,,,,,,
mondo:0014269,combined oxidative phosphorylation deficiency 19,"['LYRM4 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 19', 'COXPD19', 'combined oxidative phosphorylation deficiency type 19', 'combined oxidative phosphorylation deficiency caused by mutation in LYRM4']",0111476,615595,,C3810055,,,,,,,,
mondo:0014270,STT3A-congenital disorder of glycosylation,"['CDG syndrome type Iw', 'CDG-Iw', 'congenital disorder of glycosylation, type Iw', 'congenital disorder of glycosylation type Iw', 'STT3A-CDG', 'congenital disorder of glycosylation type 1w', 'CDG1W', 'CDG Iw', 'congenital disorder of glycosylation, type Iw, autosomal recessive']",0080572,615596,370921,C3810062,"['-0.339', '0.1462', '0.33', '-0.2053', '0.2274', '-0.5195', '-0.04886', '0.364', '-0.3608', '-0.2715', '-0.1301', '-0.2727', '0.04288', '-0.2878', '-0.1586', '0.1176', '0.1294', '-0.2094', '-0.3557', '-0.719', '0.1722', '0.10504', '0.1327', '-0.2028', '0.3535', '-0.0949', '-0.1381', '-0.08514', '0.2125', '-0.233', '0.1925', '0.2296', '0.5327', '0.2246', '-0.1475', '-0.134', '-0.2174', '-0.1081', '-0.449', '-0.2065', '-0.04312', '-0.4338', '0.0738', '0.1589', '-0.2012', '-0.1747', '-0.003944', '0.06934', '0.366', '0.3638', '-0.2698', '0.1519', '-0.008835', '0.122', '-0.11237', '-0.273', '0.141', '0.1755', '-0.2448', '0.424', '0.1963', '0.0652', '0.3896', '0.007195', '-0.0219', '-0.09644', '0.0802', '0.3257', '-0.6147', '0.04526', '-0.2864', '0.2415', '0.2651', '0.05014', '0.0275', '0.1225', '0.4915', '-0.0802', '-0.3787', '0.3477', '0.2131', '0.05084', '-0.347', '0.256', '0.1881', '-0.0159', '0.114', '0.4946', '0.3962', '0.353', '0.05188', '0.539', '-0.05557', '0.0412', '0.2415', '0.5205', '0.4875', '-0.333', '0.4004', '0.3503']",,,,,,,
mondo:0014271,STT3B-congenital disorder of glycosylation,"['CDG IX', 'STT3B-CDG', 'congenital disorder of glycosylation, type IX', 'congenital disorder of glycosylation type 1x', 'CDG1X', 'CDG-Ix', 'carbohydrate deficient glycoprotein syndrome type IX', 'CDG syndrome type IX', 'congenital disorder of glycosylation type IX']",0080573,615597,370924,C2931007,"['-0.4758', '0.05325', '0.49', '-0.4731', '0.1672', '-0.4207', '-0.1148', '0.657', '-0.4', '-0.523', '-0.1565', '-0.4248', '-0.319', '-0.1823', '-0.1636', '-0.1199', '0.275', '-0.0169', '-0.513', '-0.6646', '0.1881', '0.05502', '-0.11835', '-0.1935', '0.3044', '-0.2284', '-0.2423', '0.042', '0.3606', '-0.467', '0.3384', '-0.1403', '0.6274', '-0.04663', '-0.2683', '-0.04736', '0.0574', '-0.288', '-0.2217', '-0.001049', '0.02975', '-0.3083', '-0.1592', '0.175', '-0.2233', '-0.1395', '0.10944', '-0.03128', '0.05087', '0.3347', '-0.4568', '0.10004', '-0.2922', '0.2095', '-0.1655', '0.1703', '0.2098', '0.304', '-0.2908', '0.56', '0.06042', '-0.004395', '0.04645', '0.4502', '-0.178', '-0.1282', '0.001993', '0.553', '-0.5483', '0.2993', '-0.3337', '0.521', '0.4102', '0.1359', '0.05545', '-0.05536', '0.5034', '0.0738', '-0.3867', '0.2744', '0.3267', '0.2445', '-0.005898', '0.218', '-0.1913', '-0.03217', '0.2458', '0.4111', '0.4583', '0.2429', '-0.144', '0.563', '0.1128', '-0.0203', '0.3518', '0.4421', '0.4182', '-0.010956', '0.3406', '0.317']",,,C535751,,,,
mondo:0014272,"palmoplantar keratoderma, Nagashima type","['PPKN', 'PPK, Nagashima type', 'palmoplantar keratoderma, Nagashima type', 'palmoplantar hyperkeratosis, Nagashima type']",,615598,140966,C3810072,"['-0.05414', '0.3218', '-0.1654', '0.03354', '0.4285', '-0.859', '-0.302', '0.133', '0.01663', '-0.0889', '-0.2115', '0.07574', '-0.313', '-0.3987', '0.2869', '0.2096', '0.322', '-0.6465', '0.1885', '-0.698', '-0.01974', '0.0936', '0.2013', '-0.1406', '0.3938', '0.4077', '-0.313', '-0.0414', '0.076', '0.0686', '-0.05222', '0.1487', '0.07935', '0.08984', '0.2001', '-0.225', '-0.1296', '-0.2883', '0.2346', '-0.10046', '0.1257', '-0.65', '-0.2905', '-0.316', '0.1134', '0.08', '-0.2705', '0.5376', '0.1799', '-0.3176', '-0.04666', '-0.0818', '0.04306', '0.1553', '-0.1451', '-0.1615', '0.681', '-0.1821', '-0.4788', '0.4128', '0.10345', '-0.02788', '0.2094', '-0.3127', '0.12445', '0.1511', '0.0704', '0.3281', '-0.2427', '0.4546', '-0.632', '-0.3706', '0.1184', '-0.03696', '0.01703', '0.2988', '0.00677', '0.0937', '0.11755', '0.1423', '0.2961', '0.298', '-0.1299', '0.1006', '0.3179', '-0.4097', '0.03934', '0.8', '0.723', '0.6626', '0.2512', '0.4988', '0.5537', '0.0707', '0.6626', '0.2379', '0.3547', '-1.0625', '0.3071', '-0.2225']",,,,,,,
mondo:0014273,microcephaly-thin corpus callosum-intellectual disability syndrome,"['intellectual developmental disorder, autosomal recessive 40', 'mental retardation, autosomal recessive 40', 'intellectual disability, autosomal recessive 40', 'mental retardation, autosomal recessive type 40', 'MRT40', 'intellectual disability, autosomal recessive type 40']",0081205,615599,397951,C3810080,"['-0.08624', '0.257', '0.8965', '-0.0349', '0.157', '-0.4724', '0.1263', '0.582', '-1.089', '-0.581', '0.04486', '-0.11426', '0.634', '0.001627', '0.5605', '-0.4448', '0.922', '0.09375', '-0.479', '-1.0', '-0.00956', '0.1829', '-0.1571', '0.1246', '0.1112', '0.2795', '0.005806', '0.4326', '0.0194', '-0.253', '-0.1095', '-0.4966', '0.903', '-0.3464', '-0.4148', '0.5527', '-0.959', '-0.4404', '-0.05704', '-0.1066', '0.4822', '0.2465', '-0.596', '-0.3477', '0.3018', '-0.2128', '0.7983', '-0.2029', '0.01222', '-0.4307', '0.1102', '-0.4937', '-0.3074', '-0.6533', '-0.1791', '0.3', '-0.8345', '0.1683', '-0.79', '0.3682', '-0.007565', '0.3767', '0.1968', '0.8413', '-0.1968', '0.0091', '0.4636', '0.2184', '-0.842', '0.3228', '-0.682', '1.033', '0.01051', '-0.461', '0.2615', '0.145', '0.5483', '-0.5923', '0.05002', '-0.2773', '-0.561', '0.5786', '0.4683', '0.803', '-0.2128', '-0.361', '0.06525', '-0.2625', '0.8667', '0.3186', '0.07135', '0.587', '-0.2332', '0.711', '-0.3992', '0.546', '1.088', '0.188', '0.7217', '-0.5913']",,,,,,,
mondo:0014274,L-ferritin deficiency,"['L-ferritin deficiency', 'L-ferritin deficiency, dominant and recessive', 'LFTD']",,615604,440731,C3810090,"['-0.00937', '0.00728', '-0.00747', '0.003288', '-0.002682', '-0.01254', '-0.00827', '0.01306', '0.002422', '-0.00687', '-0.01038', '0.001038', '0.005875', '0.006336', '0.002447', '0.002584', '0.006805', '0.006626', '-0.00154', '-0.013336', '0.0076', '-0.001752', '0.01631', '-5.03e-05', '0.003746', '-0.00402', '0.002949', '0.001195', '-0.002209', '0.0002073', '0.013695', '0.004875', '0.004158', '0.00438', '0.001283', '-0.002527', '-0.001392', '-0.001415', '-0.004864', '-0.001361', '0.01139', '-0.0152', '0.0121', '0.00288', '-0.00819', '-0.00855', '-0.00331', '0.00454', '0.003717', '0.00557', '0.0002193', '-0.0011015', '0.006313', '0.01051', '0.00281', '-0.00989', '0.01733', '-0.013664', '-0.01505', '0.01062', '0.001466', '-0.001609', '0.003523', '0.004005', '0.00823', '0.004208', '0.0187', '0.000997', '-0.001955', '0.003033', '0.001723', '-0.003122', '0.004017', '-0.007404', '0.000717', '0.01631', '0.01174', '-0.004932', '0.00399', '-0.00902', '-0.006092', '-0.001372', '-0.00588', '0.015305', '0.01188', '0.003914', '0.011566', '0.0004034', '0.01531', '0.004646', '0.002691', '0.013245', '-0.004665', '0.005173', '0.00832', '0.00895', '0.010956', '-0.00734', '-0.001624', '0.01145']",,,,,,,
mondo:0014275,Fanconi renotubular syndrome 3,"['Fanconi renotubular syndrome type 3', 'FRTS3', 'EHHADH Fanconi syndrome', 'Fanconi renotubular syndrome 3', 'Fanconi syndrome caused by mutation in EHHADH']",0080759,615605,,C3810100,,,,,,,,
mondo:0014276,combined immunodeficiency due to CD3gamma deficiency,"['IMD17', 'CD3 deficiency', 'SCID-like immunodeficiency, T cell-partial, B cell-positive, NK cell-positive', 'immunodeficiency 17, CD3 gamma deficient', 'immunodeficiency 17', 'immunodeficiency type 17', 'CD3-gamma deficiency', 'CD3gamma deficiency']",0111973,615607,169082,C4510864,"['-0.4634', '0.29', '-0.002468', '0.0465', '0.0354', '-0.1208', '0.4177', '-0.074', '-0.03802', '-0.0752', '0.0374', '0.3723', '-0.2437', '0.27', '0.2556', '-0.177', '-0.151', '-0.4023', '0.0574', '-0.5566', '-0.2778', '-0.2483', '0.926', '0.1007', '0.3633', '0.1256', '-0.01522', '-0.1514', '-0.5615', '-0.411', '0.4102', '0.3118', '0.7524', '0.3972', '-0.1935', '-0.1262', '-0.562', '0.559', '-0.661', '-0.499', '-0.12', '-0.0611', '0.0653', '-0.2837', '-0.553', '-0.3884', '-0.1719', '-0.687', '0.1942', '0.362', '0.4456', '0.11725', '0.1735', '0.1317', '-0.5312', '-0.2267', '0.1819', '-0.723', '-0.1272', '0.1732', '-0.1084', '0.4375', '0.3875', '0.1112', '0.5073', '0.2365', '0.7124', '0.4702', '0.01406', '0.4258', '-0.0826', '-0.1377', '-0.0752', '0.3445', '0.4287', '-0.1838', '0.332', '-0.009384', '0.5723', '-0.04654', '-0.323', '0.1931', '0.374', '0.4216', '-0.11365', '0.01883', '0.1423', '0.0388', '0.853', '-0.0997', '0.4297', '0.975', '-0.3884', '-0.07916', '0.6416', '0.6504', '0.1544', '-0.4834', '-0.188', '0.12415']",,,,,,,
mondo:0014277,developmental dysplasia of the hip 2,"['DDH2', 'developmental dysplasia of the hip 2']",,615612,,C3715079,,,,,,,,
mondo:0014278,immunodeficiency 18,"['immunodeficiency 18', 'IMD18', 'immunodeficiency 18, Severe combined immunodeficiency variant', 'immunodeficiency type 18', 'immunodeficiency 18, SCID variant', 'CD3-Epsilon deficiency']",0111971,615615,,C3810127,,,,,,,,
mondo:0014280,immunodeficiency 19,"['CD3D', 'immunodeficiency 19', 'CD3delta deficiency', 'CD3D severe combined immunodeficiency (disease)', 'IMD19', 'SCID, T cell-negative, B cell-positive, NK cell-positive', 'immunodeficiency type 19', 'CD3-Delta deficiency', 'severe combined immunodeficiency, T cell-negative, B cell-positive, NK cell-positive']",0111972,615617,,C3810147,,,,,,,,
mondo:0014281,"cholangiocarcinoma, susceptibility to","['Chlc, susceptibility to', 'cholangiocarcinoma, susceptibility to']",,615619,,,,,,,,,,
mondo:0014282,hereditary spastic paraplegia 72,"['REEP2 pure hereditary spastic paraplegia', 'autosomal spastic paraplegia type 72', 'hereditary spastic paraplegia type 72', 'SPG72', 'pure hereditary spastic paraplegia caused by mutation in REEP2', 'spastic paraplegia 72, autosomal recessive', 'spastic paraplegia 72, autosomal dominant']",0110817,615625,401849,C3810160,"['-0.2966', '0.1371', '-0.2119', '-0.327', '-0.1824', '-0.8843', '-0.242', '0.0794', '-0.658', '-0.2998', '0.101', '0.1584', '-0.1841', '0.286', '0.693', '0.308', '-0.2325', '-0.3435', '0.1741', '-0.3782', '0.1487', '-0.1122', '0.285', '0.263', '0.118', '0.2612', '0.3416', '0.03165', '-0.386', '-0.2446', '0.1702', '0.1658', '0.1251', '0.5874', '0.1153', '-0.591', '-0.2625', '-0.2485', '-0.09894', '-0.2922', '0.05423', '-0.5093', '-0.06525', '0.3547', '-0.0529', '-0.4263', '-0.3638', '0.5063', '0.1251', '0.1243', '-0.1797', '0.0799', '-0.4563', '-0.392', '0.1229', '-0.7573', '0.864', '-0.07465', '-0.1581', '0.2773', '-0.0781', '-0.05756', '0.3005', '0.1942', '-0.654', '0.3794', '0.2484', '0.6484', '-0.12445', '0.481', '-0.2373', '-0.145', '0.1654', '-0.5366', '0.8906', '0.462', '-0.3228', '0.2903', '-0.03342', '-0.1898', '-0.137', '-0.332', '0.511', '0.849', '0.192', '-0.1721', '0.0944', '0.129', '0.0786', '-0.066', '0.6987', '-0.2167', '0.0979', '0.391', '0.8164', '0.6343', '0.783', '0.01978', '-0.0882', '0.003046']",,,,,,,
mondo:0014283,autosomal dominant nonsyndromic hearing loss 56,"['DFNA56', 'autosomal dominant nonsyndromic deafness type 56', 'deafness, autosomal dominant 56', 'deafness, autosomal dominant type 56', 'autosomal dominant nonsyndromic deafness 56', 'autosomal dominant deafness 56', 'autosomal dominant nonsyndromic deafness caused by mutation in TNC', 'TNC autosomal dominant nonsyndromic deafness']",0110581,615629,,C3810170,,,,,,,,
mondo:0014284,short-rib thoracic dysplasia 10 with or without polydactyly,"['SRTD10', 'short-rib thoracic dysplasia 10 with or without polydactyly']",0110091,615630,,C3810175,"['-0.0427', '0.042', '0.010666', '-0.03186', '0.02187', '-0.0439', '0.0108', '0.07184', '-0.0542', '-0.05988', '-0.0201', '-0.0153', '0.00538', '0.01593', '-0.02841', '-0.02824', '0.0009036', '-0.04172', '-0.03394', '-0.1148', '-0.006187', '0.002113', '0.0652', '-0.012924', '0.01157', '-0.003286', '-0.01941', '-0.01075', '0.02098', '-0.04437', '0.0496', '-0.03522', '0.0729', '0.005512', '0.02814', '-0.0236', '-0.01634', '-0.03467', '-0.015465', '-0.05698', '0.010735', '-0.0647', '0.01808', '-0.03174', '-0.002264', '-0.0395', '-0.02498', '0.05777', '0.0003607', '0.0185', '-0.000665', '-0.01223', '0.02007', '0.02115', '-0.0352', '-0.04398', '0.0359', '-0.0337', '-0.0729', '0.002775', '0.0466', '0.04074', '-0.01262', '0.009224', '-0.01133', '-0.009315', '0.05685', '0.05515', '-0.05533', '0.0721', '-0.0382', '0.01576', '0.0555', '-0.04355', '0.03616', '0.03024', '0.00947', '0.001476', '-0.0603', '-0.05405', '-0.00614', '0.0095', '0.002687', '0.04526', '-0.012215', '0.011566', '0.011116', '0.0683', '0.0719', '0.01169', '-0.01636', '0.02986', '0.001854', '0.02557', '0.1231', '0.003452', '0.05585', '-0.09', '0.00208', '0.0289']",,,,,,,
mondo:0014285,congenital dyserythropoietic anemia type type 1B,"['CDA, type IB', 'anemia, congenital dyserythropoietic, type IB', 'dyserythropoietic anemia, congenital, type IB', 'CDAN1B']",0111397,615631,,C3810185,,,,,,,,
mondo:0014286,"neuropathy, hereditary sensory, type 1F","['ATL3 hereditary sensory and autonomic neuropathy type 1', 'neuropathy, hereditary sensory, type IF', 'hereditary sensory neuropathy type IF', 'HSN1F', 'hereditary sensory and autonomic neuropathy type 1 caused by mutation in ATL3', 'hereditary sensory neuropathy type 1F', 'HSN 1F']",0070154,615632,,C3810194,,,,,,,,
mondo:0014287,short-rib thoracic dysplasia 11 with or without polydactyly,"['short-rib thoracic dysplasia 11 with or without polydactyly', 'SRTD11']",0110095,615633,,C3810200,,,,,,,,
mondo:0014288,Joubert syndrome 21,"['Joubert syndrome type 21', 'JBTS21', 'Joubert syndrome caused by mutation in CSPP1', 'Joubert syndrome 21', 'CSPP1 Joubert syndrome']",0110990,615636,,C3810212,,,,,,,,
mondo:0014289,macrocephaly-developmental delay syndrome,"['intellectual disability, autosomal recessive type 41', 'MRT41', 'mental retardation, autosomal recessive type 41', 'intellectual disability, autosomal recessive 41', 'mental retardation, autosomal recessive 41']",0081206,615637,397612,C3810225,"['0.03754', '0.3477', '0.4011', '-0.867', '-0.3616', '-0.2039', '0.6953', '0.3362', '-0.581', '-0.1604', '-0.2092', '-0.01985', '-0.2338', '-0.1648', '-0.0522', '-0.10315', '0.2998', '-0.0827', '-0.1746', '-0.4287', '0.1064', '0.1627', '0.07324', '-0.2324', '0.5645', '-0.0914', '-0.12384', '-0.1814', '0.169', '0.05356', '0.287', '-0.2554', '0.3726', '0.0727', '0.3772', '-0.1401', '-0.3315', '-0.1766', '-0.4624', '-0.667', '0.2379', '-0.5273', '-0.269', '-0.08936', '0.2317', '-0.3809', '0.0637', '0.5513', '-0.2927', '0.4407', '-0.3965', '0.341', '-0.1292', '0.1285', '-0.1924', '-0.04495', '-0.4846', '0.00961', '-0.1367', '0.07544', '0.0937', '0.1553', '-0.2247', '-0.2244', '0.05466', '-0.1519', '0.2292', '0.2905', '-0.3115', '0.55', '-0.3308', '0.5273', '-0.1571', '0.0755', '-0.658', '0.5483', '0.7676', '-0.3772', '-0.4016', '-0.28', '0.2612', '0.1132', '0.05307', '0.5234', '0.4824', '-0.07367', '-0.2856', '0.6074', '0.7207', '0.2378', '-0.2915', '0.6523', '0.508', '0.322', '0.3528', '0.6416', '0.5615', '0.0598', '0.6035', '0.02805']",,,,,,,
mondo:0014290,neurodegeneration with brain iron accumulation 6,"['neurodegeneration with brain iron accumulation due to COASY mutation', 'CoPAN', 'neurodegeneration with brain iron accumulation 6', 'NBIA6', 'COASY protein-associated neurodegeneration', 'neurodegeneration with brain iron accumulation caused by mutation in COASY', 'neurodegeneration with brain iron accumulation type 6', 'COASY neurodegeneration with brain iron accumulation']",0110740,615643,397725,C3810230,"['-0.3665', '0.5913', '0.2273', '-0.1197', '-0.2072', '-0.6753', '-0.2223', '0.0935', '-0.3552', '0.1793', '-0.2764', '-0.09576', '-0.1584', '0.051', '0.527', '-0.345', '-0.06158', '-0.4768', '-0.1326', '-0.571', '-0.11224', '-0.2426', '-0.02338', '-0.04633', '-0.02223', '0.1516', '0.2267', '-0.4407', '-0.5767', '-0.2915', '0.1577', '0.3252', '0.4348', '0.36', '0.2292', '-0.1582', '-0.2386', '-0.5107', '-0.3025', '-0.0648', '0.4158', '-0.612', '-0.1243', '0.3877', '0.4192', '-0.5757', '-0.1572', '0.315', '-0.1876', '0.1406', '0.00968', '0.462', '-0.11694', '-0.1373', '0.2213', '-0.394', '0.46', '-0.05927', '-0.2323', '0.06903', '-0.035', '-0.2208', '0.2341', '-0.318', '-0.574', '-0.1561', '0.425', '0.4197', '-0.1837', '0.3564', '-0.1898', '-0.411', '0.1404', '-0.0913', '0.1012', '0.1484', '-0.1048', '0.2261', '-0.04132', '-0.3352', '0.08344', '-0.684', '0.05804', '0.6655', '0.588', '0.1534', '0.086', '0.1793', '0.721', '0.2864', '0.522', '0.53', '0.167', '0.1909', '0.4673', '0.2942', '0.5186', '0.3315', '0.1865', '0.05215']",,,,,,,
mondo:0014291,autosomal dominant nonsyndromic hearing loss 54,"['autosomal dominant deafness 54', 'deafness, autosomal dominant 54', 'autosomal dominant nonsyndromic deafness 54', 'DFNA54', 'autosomal dominant nonsyndromic deafness type 54']",0110580,615649,,,,,,,,,,
mondo:0014292,leukoencephalopathy with mild cerebellar ataxia and white matter edema,"['LKPAT', 'leukoencephalopathy with ataxia']",,615651,363540,C3810242,"['-0.127', '-0.248', '0.1733', '-0.1179', '-0.01248', '-0.844', '0.03174', '0.11456', '-0.5146', '-0.7314', '0.0679', '0.039', '-0.2664', '0.00867', '0.5684', '-0.2915', '-0.2117', '-0.2465', '-0.0575', '-0.696', '-0.2096', '-0.4507', '0.0922', '-0.6', '0.4607', '-0.5137', '-0.3347', '0.1763', '-0.229', '-0.5625', '0.0692', '0.3413', '-0.3643', '-0.3337', '0.2228', '0.2534', '-0.2333', '-0.1237', '0.4111', '0.4048', '0.455', '0.1497', '-0.364', '0.4253', '0.5986', '-0.3865', '0.2157', '0.4268', '0.495', '0.01636', '-0.2014', '0.366', '-0.03253', '-0.4033', '-0.0713', '-0.66', '0.4863', '0.4705', '-0.1005', '0.4092', '-0.535', '0.1523', '0.4863', '-0.1611', '-0.577', '0.4795', '0.1985', '0.692', '-0.532', '0.608', '0.6943', '0.552', '-0.1267', '-0.6196', '0.5454', '0.245', '0.2095', '0.3926', '0.2263', '0.534', '-0.3481', '-0.714', '0.4004', '0.817', '-0.2725', '-0.4656', '0.2377', '-0.1805', '0.536', '0.687', '0.1539', '0.4094', '0.07477', '0.04764', '0.978', '1.025', '0.3452', '0.3735', '-0.3735', '0.129']",C171603,,,,,,
mondo:0014293,autosomal dominant nonsyndromic hearing loss 58,"['deafness, autosomal dominant 58', 'autosomal dominant nonsyndromic deafness 58', 'autosomal dominant nonsyndromic deafness type 58', 'autosomal dominant deafness 58', 'DFNA58']",0110582,615654,,,,,,,,,,
mondo:0014294,chromosome 15q11.2 deletion syndrome,"['monosomy 15q11.2', '15q11.2 microdeletion syndrome', 'chromosome 15q11.2 deletion', '15q11.2 BP1-BP2 microdeletion syndrome', 'chromosome 15q11.2 microdeletion', 'Del(15)(q11.2)', '15q11.2 microdeletion', 'chromosome 15q11.2 deletion syndrome']",0060393,615656,261183,C3180937,,,,,,,,
mondo:0014295,hereditary spastic paraplegia 57,"['SPG57', 'autosomal recessive spastic paraplegia type 57', 'spastic paraplegia due to partial TFG deficiency', 'hereditary spastic paraplegia caused by mutation in TFG', 'spastic paraplegia 57, autosomal recessive', 'hereditary spastic paraplegia type 57', 'TFG hereditary spastic paraplegia', 'autosomal recessive spastic paraplegia 57']",0110809,615658,431329,C4510084,"['-0.593', '0.3372', '0.554', '0.416', '-0.5054', '-0.72', '-0.3923', '0.126', '-0.8096', '-0.4602', '-0.06506', '0.7544', '-0.514', '-0.3792', '0.1792', '-0.4136', '0.6636', '0.08496', '-0.2233', '-0.592', '-0.06006', '-0.59', '-0.09644', '0.604', '-0.121', '0.4863', '0.0397', '0.572', '-0.3423', '-0.2382', '0.2456', '-0.012566', '0.4998', '-0.1705', '-0.0819', '-0.897', '-0.1898', '0.0947', '0.1261', '-0.3887', '-0.1301', '-0.4429', '0.1016', '0.2299', '-0.3176', '-0.5493', '0.269', '-0.126', '0.3674', '-0.1409', '-0.2257', '-0.3352', '-0.534', '-0.2864', '0.311', '-0.5034', '0.776', '-0.635', '-0.711', '0.1439', '-0.06036', '-0.0851', '0.587', '0.717', '0.103', '0.608', '0.2074', '0.359', '-0.0327', '0.2225', '-0.4412', '0.1753', '0.5596', '0.014496', '0.7344', '0.382', '0.2106', '0.997', '-0.2502', '-0.2544', '0.11304', '-0.2458', '0.921', '0.778', '0.2029', '0.1898', '-0.2507', '0.1619', '0.5947', '0.1597', '0.4724', '0.427', '-0.1638', '-0.335', '0.409', '0.625', '0.1451', '-0.1', '-0.1774', '0.602']",,0009017,,,,,
mondo:0014296,Warburg micro syndrome 4,"['Warburg micro syndrome caused by mutation in TBC1D20', 'TBC1D20 Warburg micro syndrome', 'WARBM4', 'WARBURG micro syndrome 4', 'Warburg micro syndrome type 4', 'Warburg micro syndrome 4', 'micro syndrome 4']",0110719,615663,,C3810265,,,,,,,,
mondo:0014297,Joubert syndrome 22,"['Joubert syndrome 22', 'PDE6D Joubert syndrome', 'Joubert syndrome caused by mutation in PDE6D', 'Joubert syndrome type 22', 'JBTS22']",0110991,615665,,C3810278,,,,,,,,
mondo:0014298,chromosome 5q12 deletion syndrome,"['PDE4D haploinsufficiency syndrome', 'chromosome 5q12 deletion syndrome']",0060421,615668,439822,C3810282,,,,,,,,
mondo:0014299,schwannomatosis 2,"['Schwannomatosis type 2', 'SWNTS2', 'SCHWANNOMATOSIS 2', 'schwannomatosis 2', 'schwannomatosis-2, susceptibility to']",,615670,,C3810283,,,,,,,,
mondo:0014300,proximal myopathy with extrapyramidal signs,"['MPXPS', 'myopathy with extrapyramidal signs']",0111335,615673,401768,C3810285,"['-0.2769', '0.151', '0.1537', '-0.4565', '-0.1488', '-0.45', '-0.08856', '0.565', '-0.607', '0.0231', '-0.258', '0.02963', '-0.1396', '-0.0712', '0.4373', '0.01051', '0.0327', '-0.1301', '-0.2296', '-0.653', '0.05215', '-0.0784', '-0.0974', '0.08746', '-0.0884', '-0.0668', '-0.01487', '-0.219', '-0.1829', '-0.1537', '0.08594', '0.04037', '0.465', '-0.1262', '0.03647', '-0.1692', '-0.3606', '-0.2317', '-0.1605', '-0.0729', '0.11365', '-0.2423', '-0.1334', '0.2559', '0.1127', '-0.2615', '0.0969', '0.3079', '-0.2281', '0.01133', '-0.2969', '0.3945', '-0.238', '-0.1398', '0.0983', '-0.3142', '0.1927', '-0.09784', '-0.286', '0.0993', '0.3079', '0.1333', '0.08777', '0.1406', '-0.628', '0.2096', '0.3616', '0.636', '-0.2764', '0.3682', '-0.3826', '0.1105', '0.11334', '-0.1924', '0.3157', '0.0811', '0.1082', '-0.1567', '0.012276', '-0.002308', '0.2512', '-0.004124', '0.03915', '0.5215', '-0.05792', '0.2559', '-0.1875', '0.184', '0.1853', '-0.1318', '0.4373', '0.276', '0.2676', '0.1365', '0.527', '0.2368', '0.4077', '0.1686', '0.1613', '0.1453']",,,,,,,
mondo:0014301,dowling-degos disease 3,"['DDD3', 'Dowling-Degos disease 3']",,615674,,C3810286,,,,,,,,
mondo:0014302,hereditary spastic paraplegia 62,"['autosomal recessive pure spastic paraplegia caused by mutation in ERLIN1', 'autosomal recessive spastic paraplegia 62', 'autosomal recessive spastic paraplegia type 62', 'SPG62', 'ERLIN1 autosomal recessive pure spastic paraplegia', 'hereditary spastic paraplegia type 62', 'spastic paraplegia 62, autosomal recessive']",0110813,615681,401785,C4284588,"['-0.02335', '0.3376', '-0.1775', '-0.518', '-0.1727', '-0.8447', '-0.5083', '0.3684', '-1.113', '-0.3289', '0.0712', '0.1755', '-0.01974', '-0.1786', '0.2502', '-0.3267', '0.1578', '-0.1855', '0.2883', '-0.4775', '-0.05292', '0.0773', '0.2717', '0.0779', '0.262', '0.4502', '0.2253', '0.1365', '-0.2422', '-0.09045', '0.0229', '0.0329', '-0.3745', '0.2449', '-0.2212', '-0.0455', '-0.195', '-0.1715', '-0.1094', '-0.4836', '-0.01578', '-0.706', '-0.4543', '0.618', '-0.005093', '-0.384', '-0.3113', '0.295', '0.03766', '-0.08105', '-0.0992', '0.5044', '-0.4707', '-0.10846', '0.001161', '-0.3845', '0.38', '-0.0971', '-0.4216', '0.1396', '-0.1732', '0.2803', '0.209', '0.4155', '-0.0907', '0.05972', '0.4126', '0.4387', '-0.3586', '0.4998', '0.0685', '0.322', '0.4307', '-0.4443', '0.594', '0.6084', '0.2219', '0.3828', '0.1366', '0.1721', '-0.2927', '0.1357', '0.672', '0.5977', '-0.2524', '0.1862', '-0.3884', '0.28', '0.0848', '-0.0624', '0.1162', '0.397', '0.3167', '0.0669', '0.3591', '0.5986', '0.5967', '0.1113', '-0.2379', '0.10986']",,,,,,,
mondo:0014303,hereditary spastic paraplegia 64,"['ENTPD1 autosomal recessive complex spastic paraplegia', 'autosomal recessive spastic paraplegia type 64', 'autosomal recessive spastic paraplegia 64', 'hereditary spastic paraplegia type 64', 'spastic paraplegia 64, autosomal recessive', 'SPG64', 'autosomal recessive complex spastic paraplegia caused by mutation in ENTPD1']",0110815,615683,401810,C4511960,"['0.2524', '0.423', '0.2324', '-0.5967', '0.1971', '-0.65', '-0.337', '0.5244', '-0.593', '-0.1256', '0.0885', '0.4338', '-0.0557', '-0.3335', '0.5967', '-0.387', '0.08545', '-0.54', '0.1084', '-0.5234', '-0.3389', '-0.112', '0.118', '-0.2297', '0.004017', '0.4563', '0.0759', '0.0935', '0.0792', '-0.4556', '-0.01025', '0.2207', '0.8223', '-0.0351', '-0.3672', '-0.622', '-0.3215', '-0.2988', '-0.5747', '-0.1887', '0.774', '-0.3755', '-0.1311', '0.09985', '-0.1564', '0.01797', '0.0513', '0.331', '0.00601', '0.03824', '0.0596', '-0.0709', '-0.734', '-0.3726', '0.3337', '-0.264', '0.5483', '0.05695', '-0.3347', '0.532', '-0.0127', '0.4358', '0.8477', '0.2499', '-0.1697', '0.1055', '0.3591', '0.4875', '-0.608', '-0.2064', '-0.009514', '0.4963', '0.4817', '-0.2394', '0.7095', '0.2773', '0.01194', '0.1581', '-0.3062', '0.04602', '0.264', '0.135', '0.345', '0.2888', '0.04755', '0.1362', '0.0937', '0.4182', '0.5547', '0.10175', '0.0387', '0.586', '-0.02855', '-0.2842', '0.6665', '0.569', '0.3005', '-0.2031', '0.0829', '0.1724']",,,,,,,
mondo:0014304,hereditary spastic paraplegia 61,"['SPG61', 'autosomal recessive spastic paraplegia type 61', 'ARL6IP1 autosomal recessive complex spastic paraplegia', 'autosomal recessive spastic paraplegia 61', 'hereditary spastic paraplegia type 61', 'autosomal recessive complex spastic paraplegia caused by mutation in ARL6IP1', 'spastic paraplegia 61, autosomal recessive']",0110812,615685,401780,C4511962,"['-0.2842', '0.501', '0.2776', '-0.1012', '-0.1164', '-0.7695', '-0.4333', '0.0496', '-0.659', '-0.08', '0.1635', '0.326', '-0.1315', '-0.4136', '0.3105', '-0.2145', '0.1787', '-0.332', '0.0766', '-0.4832', '0.0628', '-0.24', '0.12366', '0.2196', '0.3918', '0.6025', '-0.1447', '0.1599', '-0.2466', '-0.3765', '0.267', '0.09265', '0.08044', '-0.08215', '-0.1913', '-0.6367', '-0.01823', '-0.06793', '-0.18', '-0.4595', '0.04065', '-0.4424', '-0.0501', '0.4172', '-0.1716', '-0.212', '-0.3257', '0.2137', '0.3606', '0.488', '-0.1256', '0.08594', '-0.3035', '-0.2827', '0.12146', '-0.638', '0.62', '-0.293', '-0.4521', '0.2715', '-0.05594', '0.1857', '0.821', '0.343', '0.3474', '0.6157', '0.241', '0.0574', '-0.6', '-0.04987', '-0.335', '0.299', '0.3865', '-0.4346', '0.662', '0.3672', '0.01201', '0.4802', '0.0686', '-0.1879', '0.007084', '-0.1631', '0.3975', '0.3665', '-0.02818', '-0.11554', '-0.1262', '0.4421', '0.492', '-0.05087', '-0.001236', '0.3186', '0.219', '-0.1353', '0.514', '0.277', '0.4065', '-0.3257', '0.1328', '0.463']",,,,,,,
mondo:0014305,hereditary spastic paraplegia 63,"['SPG63', 'AMPD2 autosomal recessive complex spastic paraplegia', 'autosomal recessive complex spastic paraplegia caused by mutation in AMPD2', 'spastic paraplegia 63', 'spastic paraplegia 63, autosomal recessive', 'autosomal recessive spastic paraplegia 63', 'hereditary spastic paraplegia type 63', 'autosomal recessive spastic paraplegia type 63']",0110814,615686,401805,C3810295,"['-0.6504', '0.1212', '0.007904', '-0.4473', '0.1217', '-0.523', '-0.613', '0.2322', '-0.5303', '-0.3171', '-0.02336', '-0.0644', '0.1243', '-0.2356', '0.846', '0.4402', '-0.3123', '-0.4858', '-0.05237', '-0.4045', '0.5586', '-0.4146', '0.4417', '0.00791', '0.2659', '-0.0962', '0.2247', '0.2556', '-0.1571', '-0.3735', '0.2568', '0.10944', '0.1307', '0.001687', '0.08185', '-0.1244', '-0.3757', '-0.433', '-0.05997', '-0.701', '0.1937', '-0.7397', '-0.0598', '0.629', '-0.2493', '-0.184', '-0.11536', '0.2793', '0.3464', '-0.04193', '0.546', '-0.1278', '-0.8364', '-0.2452', '-0.1598', '-0.722', '0.3708', '-0.561', '-0.4663', '0.6597', '-0.2534', '0.2393', '0.3662', '0.1952', '-0.6333', '0.0726', '0.2302', '0.337', '-0.3142', '0.3826', '-0.3184', '0.1251', '0.05', '-0.286', '0.8916', '0.285', '-0.01117', '0.2233', '-0.259', '-0.2343', '0.1434', '-0.1804', '0.6333', '1.078', '-0.4167', '-0.06555', '0.1539', '0.3496', '0.3704', '-0.00882', '0.1256', '0.3777', '0.1014', '0.3394', '0.626', '0.4412', '0.4915', '0.02313', '0.2384', '-0.2009']",,,,,,,
mondo:0014306,vasculitis due to ADA2 deficiency,"['ADA2 deficiency', 'childhood-onset polyarteritis nodosa', 'PAN', 'adenosine deaminase 2 deficiency', 'vasculitis due to DADA2', 'vasculitis, autoinflammation, immunodeficiency, and hematologic defects syndrome', 'DADA2', 'polyarteritis nodosa, childhood-onset']",,615688,404553,C0031036,,,,,,,,
mondo:0014307,Dowling-Degos disease 4,"['DDD4', 'POGLUT1 Dowling-Degos disease', 'Dowling-Degos disease 4', 'Dowling-Degos disease caused by mutation in POGLUT1', 'Dowling-Degos disease type 4']",,615696,,C3810313,,,,,,,,
mondo:0014308,familial temporal lobe epilepsy 6,"['ETL6', 'epilepsy, familial temporal lobe, 6', 'familial temporal lobe epilepsy type 6']",0060749,615697,,C3810320,,,,,,,,
mondo:0014309,obesity due to CEP19 deficiency,"['morbid obesity and spermatogenic failure', 'MOSPGF']",,615703,397615,C3810324,"['-0.3264', '0.447', '-0.0464', '0.871', '-0.12146', '-0.8223', '0.219', '0.584', '-0.04208', '-0.588', '-0.2126', '0.27', '0.1813', '0.11285', '-0.6445', '-0.671', '-0.3843', '0.9863', '-0.5757', '-0.868', '0.0665', '-0.2642', '0.2576', '-0.2045', '0.1444', '0.3518', '-0.3218', '-0.5034', '0.1621', '-0.1702', '0.4392', '-0.535', '0.3623', '-0.01095', '-0.2186', '-0.621', '-0.8726', '0.2437', '0.6074', '0.05347', '0.0661', '0.02278', '-0.7373', '0.3396', '-0.062', '-0.7114', '0.542', '0.11084', '0.3318', '0.05264', '-0.3918', '-0.07446', '0.6006', '-0.073', '-0.1478', '0.5854', '-0.207', '0.00417', '0.03317', '-0.4456', '0.6045', '0.5103', '-0.3713', '-0.7236', '-0.2357', '0.6963', '-0.3774', '0.5635', '0.4478', '0.4602', '0.2086', '0.4814', '-0.004684', '-0.215', '0.253', '-0.6987', '-0.07947', '-0.1808', '-1.288', '0.708', '-0.0537', '0.9575', '0.006687', '0.1376', '1.012', '0.772', '0.3381', '0.1615', '0.9014', '0.5645', '-0.2957', '0.2593', '-0.1411', '0.6875', '0.667', '0.1903', '0.07007', '-0.2773', '-0.2876', '-0.0139']",,,,,,,
mondo:0014310,hereditary sclerosing poikiloderma with tendon and pulmonary involvement,"['POIKTMP syndrome', 'poikiloderma, hereditary sclerosing, with tendon and pulmonary involvement', 'hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis', 'hereditary fibrosing poikiloderma-tendon contractures-myopathy-pulmonary fibrosis syndrome', 'poikiloderma, hereditary fibrosing, with tendon contractures, myopathy, and pulmonary fibrosis', 'POIKTMP']",,615704,221043,C3810325,"['-0.2455', '-0.0818', '0.1313', '-0.551', '0.02542', '-0.361', '0.00893', '0.4187', '-0.4768', '0.1995', '-0.2161', '0.2717', '-0.0829', '-0.1498', '-0.05875', '-0.04028', '0.379', '0.0517', '-0.1421', '-0.6357', '0.0497', '-0.1809', '0.242', '0.1608', '0.10455', '0.1763', '0.05087', '0.02667', '-0.02809', '-0.3464', '0.00808', '-0.08026', '0.3171', '-0.03198', '0.132', '-0.4067', '-0.56', '-0.2869', '0.03067', '0.1368', '-0.2632', '-0.0651', '-0.1534', '0.3728', '-0.03555', '-0.0876', '-0.2544', '0.2266', '-0.03036', '-0.2166', '-0.411', '0.2289', '0.2158', '0.08246', '-0.3425', '-0.2651', '0.2588', '-0.2932', '-0.3762', '-0.1296', '0.1489', '-0.1747', '-0.1353', '0.01866', '-0.1654', '-0.0203', '0.3306', '0.6914', '-0.1399', '0.2448', '-0.5415', '-0.138', '0.2856', '0.05225', '0.3806', '-0.3433', '0.02061', '0.1174', '0.1324', '-0.2917', '-0.1453', '0.0895', '0.2056', '0.09705', '-0.4226', '-0.0325', '0.0726', '0.421', '0.1779', '-0.1387', '0.4316', '0.1731', '0.2378', '0.0887', '0.7144', '0.12067', '0.7256', '-0.1962', '-0.02843', '0.3398']",,,,,,,
mondo:0014311,autosomal recessive spinocerebellar ataxia 15,"['spinocerebellar ataxia, autosomal recessive type 15', 'SCAR15', 'RUBCN autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome', 'autosomal recessive spinocerebellar ataxia type 15', 'Salih ataxia', 'autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome due to RUBCN deficiency', 'autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome due to KIAA0226 deficiency', 'autosomal recessive cerebellar ataxia-epilepsy-intellectual disability syndrome caused by mutation in RUBCN', 'RUBCN autosomal recessive cerebellar ataxia - epilepsy - intellectual disability syndrome', 'spinocerebellar ataxia, autosomal recessive 15']",0080057,615705,404499,C3810326,"['-0.3042', '-0.3042', '0.2072', '-0.2401', '-0.251', '-0.9766', '0.1081', '0.284', '-0.7266', '-1.082', '0.2986', '0.4011', '-0.014', '0.1609', '0.5566', '-0.3442', '0.06192', '-0.3037', '0.0451', '-0.974', '-0.00105', '-0.1606', '0.02193', '-0.6064', '0.46', '-0.459', '-0.2646', '0.1576', '-0.2361', '-0.958', '0.010735', '0.4456', '-0.413', '0.05408', '0.2927', '-0.147', '-0.3354', '0.0828', '0.316', '0.3918', '0.363', '0.11316', '-0.5415', '0.546', '0.3772', '-0.4673', '-0.04388', '0.4292', '0.2296', '-0.0794', '-0.2306', '0.3271', '-0.3386', '-0.644', '-0.2039', '-0.741', '0.2888', '0.4976', '-0.1061', '0.4263', '-0.5693', '-0.10736', '0.3733', '-0.27', '-0.4653', '0.517', '0.1871', '0.5977', '-0.529', '0.375', '0.8037', '0.506', '-0.1703', '-0.793', '0.775', '0.3337', '0.2598', '0.2905', '0.4353', '0.527', '-0.4348', '-0.807', '0.4897', '0.9146', '-0.02412', '-0.561', '-0.05795', '-0.04358', '0.618', '0.592', '0.5273', '0.568', '-0.06744', '0.2075', '1.185', '1.144', '0.3157', '0.3972', '-0.09064', '-0.09']",,,,,,,
mondo:0014312,auriculocondylar syndrome 3,"['AURICULOCONDYLAR syndrome 3', 'Auriculocondylar syndrome type 3', 'Auriculocondylar syndrome 3', 'ARCND3']",,615706,,C3810332,,,,,,,,
mondo:0014313,autosomal recessive primary immunodeficiency with defective spontaneous natural killer cell cytotoxicity,"['autosomal recessive primary immunodeficiency with defective spontaneous NK cell cytotoxicity', 'immunodeficiency type 20', 'IMD20', 'immunodeficiency 20', 'CD16 deficiency']",0111941,615707,437552,C3810342,,,,,,,,
mondo:0014314,sacral agenesis-abnormal ossification of the vertebral bodies-persistent notochordal canal syndrome,"['sacral agenesis with vertebral anomalies', 'SAVA']",,615709,397927,C3810343,"['-0.4443', '-0.001488', '0.4006', '-0.25', '0.422', '-0.1469', '-0.1208', '0.3613', '-0.2311', '-0.1107', '-0.3594', '-0.2751', '0.02255', '0.0637', '-0.3655', '-0.04105', '0.05923', '-0.0999', '-0.2224', '-0.3247', '0.12054', '0.1333', '0.3257', '-0.02776', '0.1842', '0.2169', '0.05103', '0.302', '0.2983', '-0.1683', '0.3208', '-0.241', '0.2893', '0.2615', '0.2517', '-0.1422', '0.09845', '-0.1256', '0.1093', '-0.6396', '-0.00643', '0.06064', '0.1489', '-0.0392', '-0.1065', '-0.3245', '0.2228', '0.2551', '-0.4', '0.01611', '-0.0603', '-0.2148', '-0.0311', '0.102', '-0.7188', '-0.2194', '-0.1092', '-0.0947', '-0.1357', '0.09955', '0.3179', '0.03796', '-0.3242', '0.0881', '-0.2031', '0.02396', '0.41', '0.2722', '-0.3418', '0.2942', '-0.3035', '0.2502', '0.0002086', '-0.1368', '-0.208', '-0.03445', '0.0638', '0.03096', '-0.349', '-0.2017', '-0.1498', '0.2593', '0.2181', '0.3809', '-0.1705', '-0.1506', '-0.1022', '0.4312', '-0.02425', '-0.1508', '-0.1576', '0.3018', '0.07745', '0.1934', '0.5747', '-0.1757', '0.4753', '-0.3713', '0.10706', '0.1343']",,,,,,,
mondo:0014316,Alzheimer disease 19,"['Alzheimer disease type 19', 'PLD3 Alzheimer disease', 'Alzheimer disease 19', 'Alzheimer disease caused by mutation in PLD3', 'Alzheimer disease 19 late onset', 'AD19', 'Alzheimer^s disease type 19', 'Alzheimer disease 19, late-onset', 'Alzheimer^s disease 19']",0110051,615711,,C3810349,,,,,,,,
mondo:0014317,pancytopenia-developmental delay syndrome,"['bone marrow failure syndrome 2', 'bone marrow failure syndrome type 2', 'BMFS2', 'Trilineage bone marrow failure-developmental delay syndrome']",,615715,401764,C3810350,"['-0.0837', '0.0766', '0.2595', '-0.3245', '0.2966', '-0.1643', '-0.1625', '0.539', '-0.3828', '-0.006474', '0.05222', '0.2454', '0.0277', '-0.05655', '0.228', '-0.2195', '0.1169', '-0.0166', '-0.1637', '-0.561', '0.0781', '-0.0972', '0.1292', '-0.4297', '0.0635', '-0.1967', '-0.00991', '-0.2449', '0.2448', '-0.132', '0.04254', '-0.1438', '0.5625', '0.2324', '0.00316', '-0.0207', '-0.3647', '-0.3074', '-0.2035', '0.139', '0.2627', '-0.202', '0.0632', '-0.05612', '-0.2988', '-0.2401', '-0.2219', '0.311', '-0.1315', '-0.08563', '-0.3284', '0.1405', '0.01602', '0.1724', '0.1221', '-0.1503', '-0.1708', '-0.0342', '-0.2499', '0.2306', '0.2305', '-0.003134', '0.00924', '-0.369', '0.1615', '-0.1576', '0.3733', '0.4324', '-0.435', '0.2415', '-0.258', '-0.0973', '0.12115', '-0.2216', '-0.005077', '-0.1611', '0.02594', '-0.09644', '-0.1252', '-0.04712', '0.1494', '0.116', '-0.0973', '0.11365', '0.1357', '-0.03574', '0.11414', '0.2244', '0.4065', '0.3696', '0.359', '0.2693', '0.08575', '-0.1038', '0.2732', '0.3345', '0.4155', '-0.10016', '0.4487', '-0.01843']",,,,,,,
mondo:0014318,hyperphosphatasia with intellectual disability syndrome 4,"['PGAP3 hyperphosphatasia-intellectual disability syndrome', 'HPMRS4', 'hyperphosphatasia with intellectual disability syndrome type 4', 'glycosylphosphatidylinositol biosynthesis defect 10', 'hyperphosphatasia-intellectual disability syndrome caused by mutation in PGAP3', 'hyperphosphatasia with mental retardation syndrome type 4', 'hyperphosphatasia with mental retardation syndrome 4', 'hyperphosphatasia with intellectual disability syndrome 4']",,615716,,C3810354,,,,,,,,
mondo:0014319,renal hypodysplasia/aplasia 2,"['renal hypodysplasia/aplasia 2', 'renal hypodysplasia/aplasia type 2', 'RHDA2', 'FGF20 renal agenesis (disease)']",,615721,,C3810359,,,,,,,,
mondo:0014320,Bosch-Boonstra-Schaaf optic atrophy syndrome,"['optic atrophy-intellectual disability syndrome', 'BBSOAS']",0112226,615722,401777,C3810363,"['-0.2407', '0.2477', '-0.03226', '-0.1373', '-0.168', '0.2183', '0.2617', '-0.05063', '-0.09766', '-0.1477', '0.1642', '-0.6284', '-0.1769', '0.0536', '0.1438', '-0.2805', '-0.2451', '0.2625', '0.0423', '-0.516', '0.401', '-0.4153', '0.345', '0.2932', '0.2496', '0.01025', '0.04782', '0.07904', '0.02963', '-0.1598', '0.1328', '-0.169', '0.88', '0.428', '-0.00848', '-0.1592', '0.00858', '-0.471', '-0.04892', '-0.4443', '0.3357', '-0.2883', '-0.323', '-0.08386', '0.1704', '-0.0509', '0.4666', '-0.1544', '0.5234', '0.01834', '-0.04123', '0.2705', '-0.2666', '-0.5234', '0.1915', '0.2426', '0.4775', '0.2864', '-0.2595', '0.2747', '-0.2177', '-0.1399', '0.04352', '0.2404', '-0.5244', '0.2795', '-0.014336', '0.948', '-0.0847', '0.4233', '-0.261', '0.02258', '0.2106', '-0.2808', '-0.397', '0.003027', '0.655', '0.4014', '-0.149', '-0.2905', '0.142', '-0.05536', '-0.4917', '0.761', '-0.02502', '-0.345', '0.1611', '0.3428', '0.2334', '0.311', '0.225', '0.2798', '-0.05545', '0.05527', '0.85', '0.05478', '0.2952', '0.5015', '0.2128', '0.4363']",,,,,H47.2,,
mondo:0014321,premature ovarian failure 8,"['STAG3 primary ovarian failure', 'primary ovarian failure caused by mutation in STAG3', 'premature ovarian failure type 8', 'premature ovarian failure 8', 'POF8']",0080865,615723,,C3810367,,,,,,,,
mondo:0014322,premature ovarian failure 9,"['Pof9', 'premature ovarian failure 9', 'HFM1 primary ovarian failure', 'premature ovarian failure type 9', 'primary ovarian failure caused by mutation in HFM1']",0080866,615724,,C3810376,,,,,,,,
mondo:0014323,retinitis pigmentosa 68,"['RP68', 'SLC7A14 retinitis pigmentosa', 'retinitis pigmentosa type 68', 'retinitis pigmentosa caused by mutation in SLC7A14', 'retinitis pigmentosa 68']",0110374,615725,,C3810380,,,,,,H35.5,,
mondo:0014324,pachyonychia congenita 3,"['pachyonychia congenita type 3', 'PC3', 'pachyonychia congenita caused by mutation in KRT6A', 'KRT6A pachyonychia congenita', 'pachyonychia congenita 3']",,615726,,C3714948,,,,,,,,
mondo:0014325,pachyonychia congenita 4,"['pachyonychia congenita 4', 'pachyonychia congenita type 4', 'pachyonychia congenita caused by mutation in KRT6B', 'PC4', 'KRT6B pachyonychia congenita']",,615728,,C3714949,,,,,,,,
mondo:0014326,nemaline myopathy 9,"['NEM9', 'KLHL41 nemaline myopathy', 'nemaline myopathy 9', 'nemaline myopathy type 9', 'nemaline myopathy caused by mutation in KLHL41']",0110929,615731,,C3810384,,,,,,,,
mondo:0014327,"palmoplantar keratoderma, nonepidermolytic, focal or diffuse","['PPKNEFD', 'autosomal dominant focal non-epidermolytic palmoplantar keratoderma with plantar blistering', 'palmoplantar keratoderma, nonepidermolytic, focal or diffuse']",0111710,615735,402003,C3810394,"['0.0865', '0.2156', '0.04813', '-0.299', '0.08453', '-0.346', '-0.1116', '0.06635', '-0.1298', '-0.0939', '-0.2253', '-0.0186', '-0.5396', '-0.11365', '-0.04153', '0.2886', '0.3706', '-0.6445', '-0.0279', '-0.8726', '-0.1941', '-0.03668', '0.1853', '0.1864', '0.0826', '0.2747', '-0.1904', '0.2642', '-0.1207', '-0.1656', '0.213', '-0.2145', '0.02959', '0.2473', '0.1528', '0.02563', '-0.294', '-0.0474', '-0.0962', '-0.2295', '0.02852', '-0.2588', '-0.010605', '-0.147', '-0.05136', '-0.1903', '-0.4766', '0.2291', '0.0575', '0.1247', '-0.1388', '-0.04672', '0.3245', '0.0959', '-0.2683', '-0.1985', '0.4502', '0.03314', '-0.405', '-0.2546', '0.10626', '-0.03946', '-0.3252', '-0.2333', '-0.0734', '0.1665', '0.4617', '0.2593', '0.02757', '0.4802', '-0.4639', '-0.1628', '0.289', '0.07446', '0.1918', '-0.236', '0.1444', '-0.04657', '0.1007', '-0.3352', '-0.1288', '0.0845', '0.2683', '0.0645', '0.1731', '-0.1896', '-0.3262', '0.395', '0.372', '0.2275', '0.2551', '0.2313', '0.165', '0.2817', '0.4307', '0.0216', '0.162', '-0.2446', '0.06995', '0.2908']",,,,,,,
mondo:0014328,"developmental and epileptic encephalopathy, 19","['developmental and epileptic encephalopathy 19', 'GABRA1 early infantile epileptic encephalopathy', 'epileptic encephalopathy, early infantile, 19', 'Early Infantile epileptic encephalopathy 19', 'EIEE19', 'epileptic encephalopathy, early infantile, type 19', 'DEE19', 'early infantile epileptic encephalopathy caused by mutation in GABRA1']",0080431,615744,,C3810400,,C142802,,,,,,
mondo:0014329,atrial standstill 2,"['cardiomyopathy, atrial dilated, with atrial standstill', 'atrial standstill type 2', 'ATRST2', 'atrial standstill caused by mutation in NPPA', 'atrial standstill 2', 'atrial dilation and standstill', 'NPPA atrial standstill']",0080663,615745,,C3810401,,,,,,,,
mondo:0014331,Moyamoya disease with early-onset achalasia,"['Moyamoya disease 6 with achalasia', 'moyamoya 6 with achalasia', 'MYMY6']",,615750,401945,C3810403,"['-0.2617', '0.4077', '-0.4902', '-0.1117', '-0.4263', '-0.385', '0.728', '0.2954', '-0.397', '-0.605', '0.2494', '-0.0797', '0.4756', '0.3738', '0.262', '-0.0995', '-0.2407', '-0.1186', '0.4824', '-0.645', '-0.3865', '0.2119', '-0.1827', '-0.0655', '-0.7485', '-0.175', '-0.423', '0.3708', '-0.1655', '-0.2686', '-0.1779', '-0.6035', '1.041', '0.02287', '-0.0849', '0.4373', '-0.11224', '-0.03976', '-0.0683', '-0.8516', '0.6025', '0.1176', '-0.233', '-0.5884', '0.6353', '0.08795', '-0.367', '0.2344', '-0.02705', '-0.1131', '-0.02425', '0.4702', '-0.498', '-0.543', '0.6294', '0.4119', '-0.3782', '0.2169', '0.0518', '0.3484', '-0.3708', '0.0219', '0.0638', '-0.1903', '-0.1759', '0.351', '-0.265', '0.7075', '-0.9443', '0.4775', '-0.3796', '0.2047', '-0.01714', '-0.04315', '0.565', '0.477', '-0.1908', '0.402', '0.266', '0.0816', '-0.3381', '-0.615', '0.2695', '-0.0405', '0.887', '-0.4468', '0.6006', '0.211', '0.7593', '0.10187', '-0.0231', '-0.1837', '0.03906', '-0.2595', '1.023', '-0.516', '-0.4807', '-0.504', '-0.461', '-0.3176']",,,,,,,
mondo:0014332,hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency,"['carbonic anhydrase 5A deficiency, hyperammonemia due to', 'CA-VA deficiency', 'carbonic anhydrase VA deficiency, hyperammonemia due to', 'CA5AD', 'carbonic anhydrase VA deficiency', 'mitochondrial carbonic anhydrase va deficiency', 'hyperammonemia due to carbonic anhydrase VA deficiency']",,615751,401948,C3810404,"['-0.6265', '0.115', '-0.4653', '-0.1837', '-0.1375', '-0.2932', '0.0815', '0.5195', '-0.0715', '0.2556', '-0.3696', '-0.1874', '0.0726', '-0.0738', '-0.32', '0.02495', '0.08386', '0.10754', '-0.3022', '-0.888', '0.01965', '-0.635', '0.251', '-0.02838', '0.1575', '-0.183', '0.1282', '-0.08765', '-0.294', '-0.1497', '0.10406', '0.4526', '0.2632', '0.541', '-0.517', '0.11993', '0.0891', '0.0292', '0.02171', '-0.163', '-0.0759', '-0.4062', '0.341', '0.1043', '-0.433', '-0.3225', '-0.2893', '-0.2174', '0.2076', '0.7744', '-0.2146', '0.098', '0.009796', '-0.1304', '0.398', '-0.1503', '0.7944', '-0.0764', '-0.3496', '0.355', '0.1019', '0.371', '0.5356', '-0.2817', '-0.1318', '-0.07385', '0.4514', '0.3286', '-0.3694', '0.299', '-0.2432', '0.03577', '-0.02916', '-0.1234', '0.3044', '0.04233', '0.452', '0.1218', '-0.176', '0.3135', '0.05814', '0.03223', '0.02365', '-0.208', '0.2705', '0.3464', '0.1952', '0.1393', '0.322', '-0.03482', '0.2104', '0.1853', '-0.2003', '-0.02916', '0.08887', '0.777', '0.4304', '-0.281', '-0.0753', '0.4382']",,,,,,,
mondo:0014333,"polymicrogyria, bilateral perisylvian, autosomal recessive","['polymicrogyria, bilateral perisylvian, autosomal recessive', 'BPPR', 'polymicrogyria, bilateral perisylvian', 'Pmgr']",,615752,,C3810405,,,,,,,,
mondo:0014334,severe combined immunodeficiency due to LCK deficiency,"['severe combined immunodeficiency due to lymphocyte-specific protein tyrosine kinase deficiency', 'immunodeficiency 22', 'immunodeficiency type 22', 'SCID due to lymphocyte-specific protein tyrosine kinase deficiency', 'IMD22', 'SCID due to LCK deficiency']",0111937,615758,280142,C4014233,"['-0.2363', '0.1456', '0.1866', '-0.2026', '0.01258', '-0.1593', '0.3113', '0.1759', '0.0372', '-0.08014', '0.1061', '0.0783', '-0.198', '-0.01813', '-0.1362', '-0.1852', '0.1871', '0.152', '-0.3394', '-0.5103', '-0.0711', '-0.414', '0.311', '-0.1553', '-0.01756', '0.02281', '0.01211', '0.0796', '-0.11804', '-0.3037', '0.0742', '0.4324', '0.3738', '0.006935', '0.0242', '-0.1879', '-0.2433', '-0.1182', '-0.1772', '-0.2164', '0.00249', '-0.1676', '0.1354', '-0.11176', '-0.3765', '-0.2397', '-0.02333', '-0.215', '0.1544', '0.2367', '-0.1809', '-0.2257', '0.2754', '0.006416', '-0.288', '0.006233', '0.0485', '-0.191', '-0.3037', '0.1229', '0.117', '0.3142', '0.04095', '-0.02232', '0.4297', '-0.003845', '0.1962', '0.17', '-0.2622', '0.3823', '-0.1335', '0.00838', '-0.1222', '-0.1448', '0.06183', '-0.1031', '0.2864', '0.05353', '0.0987', '0.1254', '-0.1986', '-0.00869', '-0.1711', '0.07104', '-0.04758', '-0.1001', '0.2416', '0.1207', '0.3557', '-0.04996', '0.3047', '0.1855', '-0.2417', '-0.02682', '0.5107', '0.648', '0.2089', '-0.3928', '-0.0132', '0.03035']",,,,,,,
mondo:0014335,diffuse cerebral and cerebellar atrophy - intractable seizures - progressive microcephaly syndrome,"['MSCCA', 'microcephaly, progressive, seizures, and cerebral and cerebellar atrophy', 'microcephaly, progressive, with seizures and cerebral and cerebellar atrophy']",,615760,404437,C4014239,"['0.001918', '0.31', '0.4187', '0.2402', '0.1589', '-0.1228', '0.2206', '0.473', '-1.108', '-0.19', '-0.0661', '-0.1414', '0.2285', '0.3408', '0.6167', '-0.1316', '0.7593', '0.2393', '-0.4028', '-1.115', '0.0758', '0.1718', '0.07135', '-0.0907', '0.1062', '0.194', '0.008896', '0.271', '0.2219', '-0.2307', '-0.3281', '-0.3894', '0.563', '-0.135', '-0.1484', '0.9585', '-0.9307', '-0.11224', '-0.0808', '-0.2238', '0.2844', '0.2238', '-0.838', '-0.5107', '0.07556', '-0.402', '0.6704', '0.2489', '0.0864', '-0.0649', '0.2961', '-0.3503', '-0.34', '-0.4966', '0.0467', '0.2054', '-0.6104', '0.315', '-0.6865', '0.2468', '-0.0341', '0.553', '0.4346', '0.365', '-0.4688', '-0.1472', '0.5225', '0.3313', '-0.9614', '0.1283', '-0.8496', '1.178', '0.3682', '-0.7886', '0.0889', '0.333', '0.6807', '-0.2103', '-0.0393', '-0.1758', '-0.4783', '0.7236', '-0.02673', '0.4805', '-0.0771', '-0.5483', '0.1179', '-0.3867', '0.9766', '0.554', '0.425', '0.2705', '-0.1186', '0.2253', '-0.546', '0.47', '0.997', '-0.253', '0.795', '-0.2307']",,,,,,,
mondo:0014336,intellectual disability-facial dysmorphism syndrome due to SETD5 haploinsufficiency,"['autosomal dominant mental retardation 23', 'intellectual developmental disorder, autosomal dominant 23', 'intellectual disability, autosomal dominant type 23', 'autosomal dominant non-syndromic intellectual disability 23', 'mental retardation, autosomal dominant type 23', 'autosomal dominant intellectual disability 23', 'MRD23', 'intellectual disability, autosomal dominant 23', 'mental retardation, autosomal dominant 23']",0070053,615761,404440,C3810406,"['-0.1974', '0.16', '0.42', '-0.4133', '0.07227', '-0.309', '0.17', '0.4326', '-0.199', '-0.3281', '-0.1704', '-0.151', '0.0704', '-0.1177', '-0.07556', '0.0613', '-0.03564', '0.0871', '-0.4998', '-0.4868', '0.01782', '0.1106', '0.05386', '-0.2305', '0.1262', '-0.0834', '-0.2443', '-0.1382', '0.3352', '-0.2119', '0.2277', '-0.06494', '0.4666', '0.2303', '0.0729', '-0.2151', '0.007656', '-0.2091', '-0.1451', '-0.2174', '0.1742', '-0.11865', '0.0271', '-0.144', '-0.0346', '-0.3486', '0.0664', '0.08167', '-0.26', '0.1007', '-0.4841', '0.2074', '-0.10736', '-0.1029', '-0.1234', '0.0739', '-0.01109', '0.09814', '-0.10077', '0.3447', '0.06052', '0.08954', '-0.001492', '0.03078', '0.1068', '-0.0206', '0.0246', '0.324', '-0.4573', '0.2354', '-0.3198', '0.03928', '-0.05295', '-0.00843', '-0.0806', '-0.1124', '0.3792', '-0.286', '-0.3135', '0.1262', '0.1099', '0.1847', '-0.1543', '0.4236', '0.1186', '0.1633', '0.1128', '0.329', '0.291', '0.17', '0.126', '0.3691', '0.05228', '-0.04367', '0.5293', '0.181', '0.3284', '-0.2756', '0.51', '0.2544']",,,,,,,
mondo:0014337,complex cortical dysplasia with other brain malformations 5,"['CDCBM5', 'cortical dysplasia, complex, with other brain malformations 5', 'TUBB2A complex cortical dysplasia with other brain malformations', 'cortical dysplasia, Complex, with Other brain malformations type 5', 'complex cortical dysplasia with other brain malformations caused by mutation in TUBB2A', 'complex cortical dysplasia with other brain malformations type 5']",0090135,615763,,C3810407,,,,,,,,
mondo:0014338,IL21-related infantile inflammatory bowel disease,"['IL21-related infantile IBD', 'IL21 deficiency', 'immunodeficiency, common variable, type 11', 'CVID11', 'immunodeficiency, common variable, 11']",0081153,615767,477661,C4014258,,,,,,,,
mondo:0014339,autosomal recessive spinocerebellar ataxia 16,"['spinocerebellar ataxia, autosomal recessive type 16', 'autosomal recessive cerebellar ataxia due to STUB1 deficiency', 'spinocerebellar ataxia autosomal recessive type 16', 'SCAR16', 'autosomal recessive spinocerebellar ataxia type 16', 'STUB1 autosomal recessive cerebellar ataxia', 'spinocerebellar ataxia, autosomal recessive 16', 'autosomal recessive cerebellar ataxia caused by mutation in STUB1']",0080029,615768,412057,C4014261,,,,,,,,
mondo:0014340,"atrial fibrillation, familial, 15","['atrial fibrillation, familial, 15', 'NUP155 familial atrial fibrillation', 'atrial fibrillation 15', 'familial atrial fibrillation caused by mutation in NUP155', 'atrial fibrillation, familial, type 15', 'ATFB15']",,615770,,C4014269,,,,,,,,
mondo:0014341,complex cortical dysplasia with other brain malformations 6,"['CDCBM6', 'complex cortical dysplasia with other brain malformations caused by mutation in TUBB', 'CDCBM56', 'cortical dysplasia, complex, with other brain malformations 6', 'cortical dysplasia, Complex, with Other brain malformations type 6', 'TUBB complex cortical dysplasia with other brain malformations', 'complex cortical dysplasia with other brain malformations type 6']",0090136,615771,,C4014283,,,,,,,,
mondo:0014342,female infertility due to zona pellucida defect,"['oocyte maturation defect 1', 'OOMD', 'oocyte maturation defect', 'OOMD1']",,615774,404466,C4014291,"['-0.622', '-0.741', '0.3174', '-0.706', '-0.1727', '-0.4573', '0.08356', '0.5483', '-0.3762', '-0.3884', '1.549', '-0.05426', '-0.2002', '1.161', '0.0745', '-0.10406', '0.11566', '0.5195', '-0.5713', '-1.315', '-0.1335', '0.1332', '0.4158', '-0.404', '0.1974', '-0.7915', '0.2314', '0.04425', '-0.572', '-0.4436', '0.4778', '-0.1796', '-0.3154', '-0.0628', '0.1897', '0.1503', '-0.2231', '0.06256', '0.0619', '-0.1886', '0.3516', '0.2888', '0.2422', '-0.3618', '0.809', '-0.8', '0.3015', '-0.7207', '0.785', '0.4165', '-0.6978', '-0.1415', '0.014465', '0.579', '-0.1255', '0.73', '0.09814', '0.1608', '-0.6743', '0.2301', '0.3127', '0.9404', '-0.07117', '0.305', '-0.275', '0.3706', '-0.1035', '0.5195', '-1.138', '0.7217', '-0.4524', '0.0951', '-0.2051', '-0.1682', '0.1301', '0.509', '0.5005', '0.3945', '-0.1774', '0.4026', '-0.0717', '0.4841', '0.1542', '-0.5874', '-0.003584', '-0.7075', '0.1434', '-0.0319', '0.297', '-0.6987', '-0.66', '0.3865', '-0.699', '1.188', '0.6494', '-0.1981', '0.201', '-0.2522', '-0.7603', '0.1272']",,,,,,,
mondo:0014343,Desbuquois dysplasia 2,"['Desbuquois dysplasia 2', 'XYLT1 Desbuquois dysplasia', 'Desbuquois dysplasia caused by mutation in XYLT1', 'Desbuquois dysplasia type 2', 'Baratela-Scott syndrome', 'DBQD2']",,615777,,C4014294,,,,,,,,
mondo:0014344,"congenital heart defects, multiple types, 4","['congenital heart defects, multiple types caused by mutation in NR2F2', 'congenital heart defects, multiple types, 4', 'CHTD4', 'NR2F2 congenital heart defects, multiple types']",,615779,,C4014310,,,,,,,,
mondo:0014345,retinitis pigmentosa 69,"['retinitis pigmentosa 69', 'retinitis pigmentosa type 69', 'retinitis pigmentosa caused by mutation in KIZ', 'KIZ retinitis pigmentosa', 'RP69']",0110410,615780,,C4014312,,,,,,H35.5,,
mondo:0014346,white sponge nevus 2,"['WSN2', 'White sponge Nevus type 2', 'white sponge nevus 2', 'WHITE sponge NEVUS 2']",0081288,615785,,C4014321,,,,,,,,
mondo:0014347,short stature with microcephaly and distinctive facies,['short stature with microcephaly and distinctive facies'],,615789,,C4014339,"['-0.0652', '0.0662', '0.0472', '-0.06616', '0.0425', '-0.0728', '0.01706', '0.1095', '-0.0898', '-0.05545', '-0.00819', '0.002565', '0.003761', '0.0154', '-0.05203', '-0.01947', '0.04358', '-0.02588', '-0.0805', '-0.1539', '0.01958', '-0.005745', '0.04318', '-0.03632', '0.03555', '-0.00959', '-0.005833', '-0.01533', '0.00949', '-0.04666', '0.0693', '-0.04907', '0.08997', '0.04767', '0.03084', '-0.01776', '-0.0311', '-0.05', '-0.01726', '-0.0734', '0.04544', '-0.072', '0.01161', '-0.00927', '-0.01213', '-0.0742', '0.00259', '0.0671', '0.00824', '0.00089', '-0.03577', '-0.001041', '-0.00222', '-0.000657', '-0.02487', '-0.06647', '0.01958', '-0.06055', '-0.07587', '0.02744', '0.03023', '0.03021', '-0.06125', '0.0443', '0.003061', '-0.006287', '0.0671', '0.08', '-0.0738', '0.0953', '-0.0891', '0.027', '0.04526', '-0.05215', '0.00739', '-0.001487', '0.01198', '-0.03973', '-0.04614', '-0.0524', '0.01189', '-0.01949', '-0.0477', '0.06616', '-0.02545', '0.02', '0.01768', '0.07684', '0.10065', '0.03336', '-0.00711', '0.0641', '0.00479', '0.04688', '0.144', '0.0193', '0.0462', '-0.09155', '0.071', '0.03836']",,,,,,,
mondo:0014348,"intellectual disability, autosomal recessive 42","['intellectual disability, autosomal recessive 42', 'glycosylphosphatidylinositol biosynthesis defect 9', 'autosomal recessive non-syndromic intellectual disability caused by mutation in PGAP1', 'mental retardation, autosomal recessive 42', 'neurodevelopmental disorder with dysmorphic features, spasticity, and brain abnormalities', 'intellectual disability, autosomal recessive type 42', 'MRT42', 'PGAP1 autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive type 42']",,615802,,C4014343,,,,,,,,
mondo:0014349,pontocerebellar hypoplasia type 10,"['non-syndromic pontocerebellar hypoplasia caused by mutation in CLP1', 'PCH10', 'CLP1-related pontocerebellar hypoplasia', 'pontocerebellar hypoplasia, type 10', 'CLP1 non-syndromic pontocerebellar hypoplasia']",0060279,615803,411493,C4014347,,,,,,,,
mondo:0014350,Seckel syndrome 8,"['Seckel syndrome 8', 'Seckel syndrome caused by mutation in DNA2', 'SCKL8', 'DNA2 Seckel syndrome', 'Seckel syndrome type 8']",0070009,615807,,C3891452,,,,,,,,
mondo:0014351,pontocerebellar hypoplasia type 9,"['pontocerebellar hypoplasia, type 9', 'AMPD2 non-syndromic pontocerebellar hypoplasia', 'non-syndromic pontocerebellar hypoplasia caused by mutation in AMPD2', 'PCH9']",0060278,615809,369920,C4014354,"['-0.3691', '0.2861', '0.3389', '-0.108', '0.1409', '-0.369', '-0.0939', '0.3682', '-0.801', '-0.3643', '-0.254', '-0.3887', '-0.1296', '-0.445', '0.556', '-0.465', '0.4797', '-0.1278', '0.297', '-0.5693', '0.0529', '0.003134', '0.2703', '-0.04172', '0.321', '-0.2092', '-0.02248', '0.0612', '-0.1167', '-0.1425', '0.03827', '0.1562', '0.4402', '0.00971', '0.1698', '0.0708', '-0.1274', '-0.04614', '0.0167', '-0.3281', '0.455', '-0.1317', '-0.2251', '0.2957', '-0.2416', '-0.4583', '-0.03445', '0.1195', '-0.1832', '-0.289', '0.293', '0.00874', '-0.1609', '-0.1179', '-0.2725', '0.00773', '0.1915', '0.106', '-0.02954', '0.5576', '-0.1349', '0.1185', '0.329', '0.00815', '-0.2401', '0.01333', '0.2842', '0.1691', '-0.4084', '0.4094', '0.0165', '0.3262', '0.3918', '-0.1821', '0.02173', '-0.2063', '0.1819', '-0.1089', '-0.633', '-0.2688', '0.0857', '-0.0801', '0.1272', '0.3757', '-0.05698', '-0.45', '-0.2308', '0.605', '0.2274', '0.1425', '0.2356', '0.346', '0.0991', '-0.1896', '0.7144', '0.2418', '0.501', '-0.1216', '0.4436', '0.0721']",,,,,,,
mondo:0014352,abdominal obesity-metabolic syndrome 3,"['abdominal obesity-metabolic syndrome type 3', 'DYRK1B metabolic syndrome', 'metabolic syndrome caused by mutation in DYRK1B', 'abdominal obesity-metabolic syndrome 3', 'central obesity, type 2 diabetes, hypertension, and early-onset coronary artery disease', 'AOMS3']",0060612,615812,,C4014361,,,,,,,,
mondo:0014353,immunodeficiency 23,"['phosphoglucomutase deficiency type 3', 'PGM3-EXACT congenital disorder of glycosylation', 'phosphoglucomutase 3 deficiency', 'immunodeficiency with hyper IgE and cognitive impairment', 'combined immunodeficiency due to PGM3 deficiency', 'CID due to PGM3 deficiency', 'IMD23', 'immunodeficiency type 23', 'combined inflammatory and immunologic defect', 'immunodeficiency-vasculitis-myoclonus syndrome', 'immunodeficiency 23']",0111953,615816,443811,C4014371,,,,C565684,,,,
mondo:0014354,"intellectual disability, autosomal recessive 43","['intellectual disability, autosomal recessive 43', 'intellectual disability, autosomal recessive type 43', 'intellectual developmental disorder, autosomal recessive 43', 'mental retardation, autosomal recessive type 43', 'mental retardation, autosomal recessive 43', 'MRT43', 'WASHC4 autosomal recessive non-syndromic intellectual disability', 'autosomal recessive non-syndromic intellectual disability caused by mutation in WASHC4']",0081207,615817,,C4014386,,,,,,,,
mondo:0014355,"cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis","['dilated cardiomyopathy with woolly hair, keratoderma, and tooth agenesis', 'cardiomyopathy, dilated, with wooly hair, keratoderma, and tooth agenesis', 'DCWHKTA', 'dilated cardiomyopathy with wooly hair, keratoderma, and tooth agenesis']",,615821,,C4014393,,,,,,,,
mondo:0014356,mitochondrial complex III deficiency nuclear type 7,"['mitochondrial complex III deficiency caused by mutation in UQCC2', 'MC3DN7', 'mitochondrial Complex 3 deficiency, nuclear type 7', 'UQCC2 mitochondrial complex III deficiency', 'mitochondrial complex III deficiency, nuclear type 7']",0080116,615824,,C4014408,,,,,,,,
mondo:0014357,"intellectual disability, autosomal dominant 24","['intellectual disability, autosomal dominant 24', 'mental retardation, autosomal dominant 24', 'autosomal dominant intellectual disability 24', 'autosomal dominant non-syndromic intellectual disability caused by mutation in DEAF1', 'autosomal dominant non-syndromic intellectual disability 24', 'mental retardation, autosomal dominant type 24', 'DEAF1 autosomal dominant non-syndromic intellectual disability', 'intellectual disability, autosomal dominant type 24', 'MRD24', 'autosomal dominant mental retardation 24', 'Vulto-van Silfout-de Vries syndrome']",0070054,615828,,C4014414,,,,,,,,
mondo:0014358,AHDC1-related intellectual disability - obstructive sleep apnea - mild dysmorphism syndrome,"['Xia-Gibbs syndrome', 'autosomal dominant intellectual disability 25', 'MRD25', 'intellectual disability, autosomal dominant 25', 'autosomal dominant mental retardation 25', 'mental retardation, autosomal dominant 25']",0070055,615829,412069,C4014419,"['-0.1294', '0.546', '-0.4824', '-0.01516', '-0.3604', '-0.3792', '0.2886', '0.733', '-0.1804', '-0.2905', '-0.004658', '-0.0088', '0.1637', '0.431', '-0.5117', '-0.7017', '-0.4236', '0.3975', '-0.4832', '-0.4631', '-0.0357', '0.401', '-0.1381', '-0.1963', '-0.338', '-0.4915', '0.05545', '-0.1835', '0.5083', '-0.1127', '0.1499', '-0.1954', '0.686', '0.1476', '-0.1562', '0.2324', '-0.1389', '-0.3918', '0.516', '-0.0969', '0.4817', '0.3025', '-0.2712', '0.03555', '-0.0373', '0.0693', '0.1234', '0.3774', '0.002552', '0.4402', '-0.308', '0.3755', '-0.02983', '-0.3228', '0.1348', '0.2028', '-0.3398', '-0.0772', '-0.2817', '-0.3384', '0.1099', '0.41', '0.0606', '-0.0173', '-0.4648', '-0.3508', '0.0266', '0.7456', '-0.2732', '0.747', '-0.3015', '0.4084', '-0.2744', '-0.533', '-0.1509', '0.4214', '0.783', '0.4297', '-0.3657', '0.4763', '-0.4136', '-0.3052', '0.2861', '0.4475', '0.716', '0.01469', '-0.301', '0.268', '0.577', '0.461', '-0.4006', '0.1166', '-0.3108', '0.495', '0.3638', '-0.1154', '-0.7417', '-0.184', '-0.4211', '0.01924']",,0009015,,,,,
mondo:0014359,"pigmented nodular adrenocortical disease, primary, 4","['Cushing syndrome, adrenal, due to Ppnad4', 'PRKACA primary pigmented nodular adrenocortical disease', 'chromosome 19P13 Duplication syndrome', 'pigmented nodular adrenocortical disease, primary, type 4', 'PPNAD4', 'ACTH-independent adrenal Cushing syndrome, somatic', 'primary pigmented nodular adrenocortical disease caused by mutation in PRKACA', 'Cushing syndrome, ACTH-independent adrenal, somatic', 'pigmented nodular adrenocortical disease, primary, 4']",,615830,,C4014425,,,,,,,,
mondo:0014360,"developmental and epileptic encephalopathy, 21","['epileptic encephalopathy, early infantile, type 21', 'epileptic encephalopathy, early infantile, 21', 'EIEE21', 'DEE21', 'developmental and epileptic encephalopathy 21', 'early infantile epileptic encephalopathy caused by mutation in NECAP1', 'NECAP1 early infantile epileptic encephalopathy']",0080443,615833,,C4014430,,,,,,,,
mondo:0014361,autism spectrum disorder due to AUTS2 deficiency,"['MRD26', 'intellectual disability type 26', 'autosomal dominant non-syndromic intellectual disability 26', 'mental retardation, autosomal dominant type 26', 'intellectual developmental disorder, autosomal dominant 26', 'autosomal dominant mental retardation 26', 'AUTS2 syndrome', 'ASD due to AUTS2 deficiency', 'mental retardation, autosomal dominant 26']",0070056,615834,352490,C4014435,"['0.2122', '0.406', '0.249', '0.2054', '0.0437', '-0.5767', '0.747', '0.7046', '-0.4397', '-0.5635', '0.9897', '0.0844', '-0.1654', '0.2588', '-0.1217', '0.436', '-0.535', '-0.1161', '-0.535', '-0.3396', '-0.4502', '-0.332', '0.2211', '-0.2292', '0.4932', '-0.502', '0.2983', '0.07184', '0.4033', '-0.356', '0.489', '-0.4548', '1.251', '0.759', '-0.01118', '-0.1444', '-0.1957', '0.4585', '0.4702', '-0.501', '0.78', '0.04614', '-0.9243', '-0.2698', '0.718', '-0.7656', '0.6406', '-0.02235', '-0.1776', '-0.02554', '-0.8887', '-0.1387', '-0.8677', '-0.0212', '0.6484', '0.02505', '-0.9146', '0.4238', '-0.0729', '0.551', '-0.01014', '0.02887', '0.2156', '0.72', '-0.382', '-0.2249', '0.7686', '0.1959', '-0.3818', '0.4995', '0.4653', '-0.02666', '-0.1277', '-0.556', '0.567', '0.4849', '0.1473', '0.4875', '0.01545', '-0.2595', '0.187', '0.4116', '-0.1085', '0.3105', '0.3484', '0.344', '-0.677', '0.2537', '0.1978', '0.831', '-0.2034', '0.4983', '-0.844', '0.0751', '0.07654', '0.358', '0.155', '-0.2482', '0.5957', '-0.1387']",,,,,,,
mondo:0014362,"chromosome 16 inversion, 0.45-Mb","['chromosome 16 inversion, 0.45-Mb']",,615835,,,,,,,,,,
mondo:0014363,autosomal recessive nonsyndromic hearing loss 101,"['deafness, autosomal recessive 101', 'deafness, autosomal recessive type 101', 'GRXCR2 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 101', 'DFNB101', 'autosomal recessive deafness 101', 'autosomal recessive nonsyndromic deafness 101', 'autosomal recessive nonsyndromic deafness caused by mutation in GRXCR2']",0110462,615837,,C3892049,,,,,,,,
mondo:0014364,mitochondrial complex III deficiency nuclear type 8,"['LYRM7 mitochondrial complex III deficiency', 'mitochondrial complex III deficiency, nuclear type 8', 'mitochondrial Complex 3 deficiency, nuclear type 8', 'MC3DN8', 'mitochondrial complex III deficiency caused by mutation in LYRM7']",0080117,615838,,C4014440,,,,,,,,
mondo:0014365,spermatogenic failure 13,"['TAF4B azoospermia', 'spermatogenic failure 13', 'SPGF13', 'azoospermia caused by mutation in TAF4B', 'spermatogenic failure type 13']",0070182,615841,,C4014449,,,,,,,,
mondo:0014366,spermatogenic failure 14,"['azoospermia caused by mutation in ZMYND15', 'spermatogenic failure 14', 'spermatogenic failure type 14', 'ZMYND15 azoospermia', 'SPGF14']",0070179,615842,,C4014454,,,,,,,,
mondo:0014367,Aicardi-Goutieres syndrome 7,"['IFIH1 Aicardi-Goutieres syndrome', 'AGS7', 'Aicardi-Goutieres syndrome type 7', 'Aicardi-Goutieres syndrome caused by mutation in IFIH1', 'Aicardi-Goutieres syndrome 7']",,615846,,C3888244,,C168585,,,,,,
mondo:0014368,"melanoma, cutaneous malignant, susceptibility to, 10","['melanoma, cutaneous malignant, susceptibility to, 10', 'melanoma, cutaneous malignant, susceptibility to, type 10', 'susceptibility to cutaneous malignant melanoma 10', 'CMM10']",,615848,,,,,,,,,,
mondo:0014369,postaxial polydactyly-anterior pituitary anomalies-facial dysmorphism syndrome,"['Culler-Jones syndrome', 'Pallister-Hall syndrome 2', 'Pallister-Hall syndrome 2, formerly', 'CJS']",0080328,615849,420584,C4014479,"['-0.0791', '0.09033', '0.05707', '-0.05136', '0.05698', '-0.05887', '0.01622', '0.1073', '-0.06775', '-0.1127', '-0.0424', '-0.03903', '0.02942', '0.02336', '-0.04843', '-0.05185', '0.01492', '-0.02954', '-0.1176', '-0.1534', '0.001083', '-0.0185', '0.0622', '-0.0737', '0.0463', '-0.03806', '-0.0604', '-0.013374', '0.0603', '-0.0917', '0.0811', '-0.03943', '0.10187', '0.03076', '0.03284', '-0.03168', '0.01895', '-0.039', '-0.04337', '-0.08563', '0.0749', '-0.06274', '0.0242', '-0.0501', '0.0478', '-0.0867', '-0.01901', '0.0922', '0.003876', '0.01272', '-0.07056', '-0.02637', '-0.00284', '0.03323', '-0.07764', '-0.04666', '0.05573', '-0.0769', '-0.0661', '0.06616', '0.06244', '0.0663', '-0.00967', '0.01572', '-0.02182', '0.011', '0.09', '0.0739', '-0.1232', '0.09174', '-0.1395', '0.042', '0.066', '-0.04144', '0.012825', '0.04865', '0.01528', '-0.01736', '-0.0717', '-0.06247', '-0.02579', '0.0224', '-0.0234', '0.1006', '-0.000515', '0.03293', '-0.0004778', '0.0947', '0.10754', '-0.01762', '0.02448', '0.1126', '0.04526', '-0.02832', '0.2197', '0.01938', '0.08923', '-0.1471', '0.04886', '0.0774']",,,,,,,
mondo:0014370,pontocerebellar hypoplasia type 2E,"['pontocerebellar hypoplasia, type 2E', 'non-syndromic pontocerebellar hypoplasia caused by mutation in VPS53', 'PCH2E', 'VPS53 non-syndromic pontocerebellar hypoplasia']",0060271,615851,,C4014488,,,,,,,,
mondo:0014371,"developmental and epileptic encephalopathy, 23","['early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome', 'epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome', 'EIEE23', 'epileptic encephalopathy, early infantile, 23', 'epileptic encephalopathy, early infantile, type 23', 'developmental and epileptic encephalopathy 23']",0080415,615859,411986,C4014492,,,,,,,,
mondo:0014372,cone-rod dystrophy 19,"['TTLL5 cone-rod dystrophy', 'CORD19', 'cone-rod dystrophy caused by mutation in TTLL5', 'cone-rod dystrophy type 19', 'cone-rod dystrophy 19']",0111025,615860,,C4014501,,,,,,,,
mondo:0014373,"nephrotic syndrome, type 10","['nephrotic syndrome, type 10', 'nephrotic syndrome caused by mutation in EMP2', 'EMP2 nephrotic syndrome', 'NPHS10']",0080386,615861,69061,C4014507,,,,,,,,
mondo:0014374,nephronophthisis 18,"['nephronophthisis type 18', 'NPHP18', 'nephronophthisis 18', 'CEP83 nephronophthisis (disease)']",0111125,615862,,C3890591,,,,,,,,
mondo:0014375,congenital diarrhea 7 with exudative enteropathy,"['diarrhea 7, protein-losing enteropathy type', 'DIAR7', 'diarrhoea type 7', 'DGAT1 congenital diarrhea', 'congenital diarrhea caused by mutation in DGAT1', 'diarrhoea 7', 'diarrhea type 7', 'diarrhea 7', 'diarrhoea 7, protein-losing enteropathy type', 'DGAT1 congenital diarrhoea', 'congenital chronic diarrhoea with protein-losing enteropathy', 'congenital chronic diarrhea with exudative enteropathy', 'congenital diarrhoea caused by mutation in DGAT1', 'congenital chronic diarrhoea with exudative enteropathy', 'congenital chronic diarrhea with protein-losing enteropathy']",0060778,615863,329242,C4014516,"['0.4949', '0.07404', '0.5005', '0.3413', '-0.555', '-0.771', '-1.127', '0.3916', '-0.1615', '0.1057', '0.7324', '0.6772', '0.3486', '0.5405', '-1.158', '0.1482', '-0.287', '0.0793', '-0.435', '-0.909', '0.08124', '-0.2107', '-0.2861', '-0.0675', '0.05', '-0.5376', '-0.823', '0.4316', '0.2546', '-1.17', '-0.1754', '-0.5293', '-0.1439', '0.4294', '0.984', '0.4597', '-0.431', '0.3694', '0.0896', '0.09375', '-0.708', '-0.6025', '-0.4233', '-0.4805', '0.5083', '0.0626', '-0.05197', '0.3767', '-0.1866', '1.116', '-0.6577', '-0.3494', '0.11755', '-0.483', '-0.003738', '-0.313', '-0.1826', '-0.09375', '-0.6274', '-0.074', '0.669', '0.658', '0.352', '-0.5327', '0.0694', '-0.3374', '0.46', '-0.0935', '0.265', '1.137', '-0.3887', '0.835', '0.1456', '-0.8115', '0.676', '0.0868', '-0.599', '0.042', '-0.04382', '0.765', '-0.254', '-0.7153', '-0.1299', '0.0505', '0.269', '0.4734', '0.6924', '0.1001', '0.05826', '-0.3', '0.04285', '-0.2228', '-0.4458', '-0.4377', '0.724', '0.851', '0.348', '-1.686', '-0.2805', '-0.3271']",,,,,,,
mondo:0014376,"intellectual disability, autosomal dominant 27","['autosomal dominant mental retardation 27', 'MRD27', 'intellectual disability, autosomal dominant 27', 'autosomal dominant non-syndromic intellectual disability 27', 'mental retardation, autosomal dominant 27', 'autosomal dominant intellectual disability 27', 'CSS9', 'mental retardation, autosomal dominant type 27', 'Coffin-Siris syndrome 9', 'intellectual disability, autosomal dominant type 27']",0070057,615866,,C4014528,,,,,,,,
mondo:0014377,"developmental and epileptic encephalopathy, 24","['epileptic encephalopathy, early infantile, 24', 'DEE24', 'EIEE24', 'early infantile epileptic encephalopathy caused by mutation in HCN1', 'developmental and epileptic encephalopathy 24', 'epileptic encephalopathy, early infantile, type 24', 'HCN1 early infantile epileptic encephalopathy']",0080429,615871,,C4014531,,,,,,,,
mondo:0014378,primary ciliary dyskinesia 29,"['ciliary dyskinesia, primary, 29, without situs inversus', 'CILD29', 'primary ciliary dyskinesia caused by mutation in CCNO', 'ciliary dyskinesia, primary, type 29', 'primary ciliary dyskinesia 29 without situs inversus', 'primary ciliary dyskinesia type 29', 'CCNO primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 29']",0110600,615872,,C4014534,,C172393,,,,,,
mondo:0014379,ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder,"['Helsmoortel-VAN DER AA syndrome', 'MRD28', 'intellectual disability, autosomal dominant 28', 'HVDAS', 'ADNP syndrome', 'autosomal dominant mental retardation 28', 'autosomal dominant intellectual disability 28', 'mental retardation, autosomal dominant 28']",0070058,615873,404448,C4014538,"['0.2102', '0.1779', '0.331', '0.08673', '0.179', '-0.3743', '0.553', '0.642', '-0.1722', '-0.448', '0.611', '0.1975', '-0.11053', '0.154', '0.23', '0.4001', '-0.4072', '-0.2556', '-0.529', '-0.2805', '-0.535', '-0.3513', '-0.1284', '-0.3425', '0.6436', '-0.5425', '0.1344', '-0.01284', '0.2598', '-0.3274', '0.484', '-0.1855', '1.011', '0.6587', '0.01956', '-0.1116', '-0.1995', '0.4053', '0.354', '-0.688', '0.8003', '0.02756', '-0.8477', '-0.3381', '0.658', '-0.7935', '0.3567', '-0.2524', '-0.212', '0.2269', '-0.5576', '0.02815', '-0.7817', '0.0816', '0.6055', '0.1595', '-0.3984', '0.3198', '0.001763', '0.2347', '-0.010765', '0.2358', '0.3018', '0.5913', '-0.1848', '-0.1608', '0.669', '0.1643', '-0.5815', '0.2473', '0.2297', '-0.1027', '-0.5713', '-0.4817', '0.812', '0.2908', '0.05847', '0.758', '-0.2542', '-0.407', '0.2798', '0.401', '-0.1411', '0.3687', '0.4922', '0.12103', '-0.3357', '0.2048', '0.262', '0.8643', '-0.2448', '0.372', '-0.753', '-0.1469', '-0.1793', '0.4583', '0.1498', '-0.5273', '0.7124', '-0.1615']",,,,,,,
mondo:0014380,colobomatous microphthalmia-rhizomelic dysplasia syndrome,"['MCOPS14', 'microphthalmia-coloboma-rhizomelic skeletal dysplasia', 'microphthalmia or coloboma with or without rhizomelic skeletal dysplasia', 'microphthalmia and coloboma, with or without rhizomelic skeletal dysplasia', 'MCSKS', 'microphthalmia/coloboma and skeletal dysplasia syndrome', 'microphthalmia, syndromic 14', 'microphthalmia, syndromic type 14']",0111802,615877,424099,C4014540,,,,,,,,
mondo:0014381,"cholestasis, progressive familial intrahepatic, 4","['PFIC4', 'cholestasis, progressive familial intrahepatic, type 4', 'TJP2 deficit', 'progressive familial intrahepatic cholestasis caused by mutation in TJP2', 'TJP2 progressive familial intrahepatic cholestasis', 'progressive familial intrahepatic cholestasis 4', 'cholestasis, progressive familial intrahepatic 4', 'cholestasis, progressive familial intrahepatic, 4']",0070224,615878,79304,CN776838,,,,,,,,
mondo:0014382,Tatton-Brown-Rahman overgrowth syndrome,"['TATTON-BROWN-Rahman syndrome', 'Tatton-Brown-Rahman overgrowth syndrome', 'TBRS', 'tall stature-intellectual disability-facial dysmorphism syndrome', 'DNMT3A-related overgrowth syndrome']",0112339,615879,404443,C4014545,"['-0.1158', '0.3293', '0.05634', '-0.03323', '0.342', '-0.409', '0.02246', '0.4849', '-0.4004', '-0.4885', '0.7817', '0.3315', '0.3188', '-0.01165', '-0.1621', '0.1637', '0.06647', '-0.1534', '-0.1959', '-0.128', '-0.0482', '-0.0851', '0.1259', '0.009026', '0.2866', '-0.224', '0.06573', '-0.2986', '0.4785', '0.1073', '0.2042', '-0.0691', '0.3896', '0.2795', '0.2467', '-0.3408', '-0.276', '-0.1523', '0.1942', '-0.4292', '0.38', '-0.2952', '-0.4102', '0.1368', '0.05023', '-0.5166', '0.3193', '0.303', '0.0682', '-0.1075', '0.1178', '-0.007133', '-0.3015', '0.1473', '0.3433', '-0.1674', '0.02313', '0.07733', '0.3848', '-0.00669', '0.04404', '0.03345', '-0.1279', '-0.03775', '-0.1605', '0.1887', '-0.0783', '0.459', '-0.2644', '0.4421', '-0.1566', '0.1769', '-0.1564', '0.1791', '-0.133', '0.1376', '0.4055', '-0.010345', '-0.1254', '-0.3354', '0.161', '-0.1571', '-0.06113', '0.3293', '-0.1486', '0.1898', '0.06183', '0.1938', '0.2852', '0.846', '-0.1698', '0.11035', '0.03574', '0.1852', '0.4133', '0.292', '0.1514', '-0.2793', '0.09485', '0.1772']",,,,,,,
mondo:0014383,"myopathy, tubular aggregate, 2","['myopathy, tubular aggregate, 2', 'ORAI1 tubular aggregate myopathy', 'TAM2', 'tubular aggregate myopathy caused by mutation in ORAI1', 'myopathy, tubular aggregate, type 2']",0080686,615883,,C4014557,,,,,,,,
mondo:0014384,hypotrichosis 12,"['hypt12', 'hypotrichosis 12', 'hypotrichosis type 12', 'hypotrichosis caused by mutation in RPL21', 'RPL21 hypotrichosis', 'HYPT12']",0110709,615885,,C4014563,,,,,,,,
mondo:0014385,amelogenesis imperfecta hypomaturation type 2A5,"['amelogenesis imperfecta, hypomaturation type, IIA5', 'amelogenesis imperfecta, type IIA5', 'amelogenesis imperfecta hypomaturation type IIA5', 'SLC24A4 amelogenesis imperfecta', 'AI2A5', 'amelogenesis imperfecta caused by mutation in SLC24A4', 'amelogenesis imperfecta type IIA5']",0110063,615887,,C4014578,,,,,,,,
mondo:0014386,platelet-type bleeding disorder 18,"['inherited bleeding disorder, platelet-type caused by mutation in RASGRP2', 'RASGRP2 inherited bleeding disorder, platelet-type', 'BDPLT18', 'bleeding disorder due to CalDAG-GEFI deficiency', 'bleeding disorder, platelet-type, 18', 'bleeding disorder due to calcium- and DAG-regulated guanine exchange factor-1 deficiency']",0111051,615888,420566,C4014584,"['-0.02594', '0.02837', '0.005035', '-0.001041', '0.01397', '-0.0332', '-0.006927', '0.03256', '-0.009995', '-0.006565', '-0.01323', '0.001795', '0.0125', '0.009384', '-0.002913', '-0.02054', '6.77e-05', '-0.01438', '-0.006523', '-0.0354', '-0.01446', '-0.02156', '0.01851', '-0.01959', '0.01173', '-0.01575', '0.008766', '-0.0003693', '-0.01248', '-0.01269', '0.0248', '0.000925', '0.01828', '0.001761', '0.00959', '-0.001786', '0.00221', '-0.01111', '-0.002237', '-0.02335', '0.01802', '-0.02113', '0.0002456', '-0.0099', '-0.002419', '-0.0305', '-0.01336', '0.02747', '0.000241', '0.007507', '-0.00469', '-0.001448', '-0.004227', '0.01791', '-0.012856', '-0.012794', '0.02115', '-0.01689', '-0.02818', '-0.001657', '0.01531', '0.02197', '0.00664', '-0.010315', '0.00831', '-0.00787', '0.03964', '0.026', '-0.036', '0.02109', '-0.02252', '0.00584', '-0.002342', '-0.02872', '0.00976', '0.0264', '0.00708', '0.00821', '-0.010796', '-0.010056', '-0.01162', '-0.00809', '-0.00848', '0.01901', '-0.00837', '-0.00532', '0.01945', '0.02669', '0.02916', '-0.007587', '0.01279', '0.03693', '-0.005123', '-0.004345', '0.05493', '0.0158', '0.0231', '-0.0342', '0.005806', '0.01335']",,,,,,,
mondo:0014387,"leukoencephalopathy, progressive, with ovarian failure","['LKENP', 'leukoencephalopathy, progressive, with ovarian failure']",,615889,,C4014588,,,,,,,,
mondo:0014388,familial median cleft of the upper and lower lips,"['orofacial cleft 14', 'OFC14']",0080407,615892,401942,,,,,,,,,
mondo:0014389,polyglucosan body myopathy 1 with or without immunodeficiency,"['PGBM1', 'polyglucosan body myopathy type 1', 'polyglucosan body myopathy 1 with or without immunodeficiency', 'polyglucosan body myopathy, early-onset, with or without immunodeficiency']",,615895,397937,C4014605,"['-0.0923', '0.1113', '-0.0043', '-0.02527', '0.0495', '-0.127', '-0.002907', '0.0884', '-0.1272', '-0.05267', '-0.0398', '0.011795', '0.04202', '0.07587', '-0.04956', '-0.06854', '-0.03937', '-0.0253', '-0.07336', '-0.1938', '0.003485', '-0.06744', '0.05505', '0.00863', '0.01604', '-0.01909', '-0.05725', '-0.04044', '-0.0415', '-0.03638', '0.0965', '0.00257', '0.0797', '0.04202', '0.06335', '-0.03119', '-0.0625', '-0.0331', '-0.00823', '-0.1176', '-0.02452', '-0.1023', '-0.00932', '0.01892', '-0.02213', '-0.0886', '0.007336', '0.07544', '0.02971', '0.05185', '-0.0275', '0.01657', '0.05142', '-0.01752', '-0.0539', '-0.0967', '0.11096', '-0.0889', '-0.1046', '-0.02719', '0.0873', '0.04904', '0.00841', '-0.00813', '-0.03064', '0.038', '0.0984', '0.07825', '-0.1119', '0.0597', '-0.0643', '0.00639', '0.009155', '-0.0378', '-0.003416', '0.09485', '-0.02136', '0.0125', '-0.04767', '-0.05103', '-0.00226', '0.0131', '0.02992', '0.0903', '0.01627', '0.02034', '-0.01457', '0.081', '0.1214', '0.01156', '0.0948', '0.0831', '0.01447', '0.0552', '0.1699', '0.08673', '0.09064', '-0.0958', '-0.02559', '0.04355']",,,,,,,
mondo:0014390,hypotrichosis 13,"['hypotrichosis 13', 'hypotrichosis caused by mutation in KRT71', 'hypotrichosis type 13', 'KRT71 hypotrichosis', 'HYPT13', 'hypt13', 'hypotrichosis with wooly hair', 'hypotrichosis with woolly hair']",0110710,615896,,C4014616,,,,,,,,
mondo:0014391,severe combined immunodeficiency due to CTPS1 deficiency,"['IMD24', 'immunodeficiency type 24', 'immunodeficiency 24', 'SCID due to CTPS1 deficiency']",0111938,615897,420573,C4014617,,,,,,,,
mondo:0014392,"developmental and epileptic encephalopathy, 25","['DEE25', 'EIEE25', 'early infantile epileptic encephalopathy caused by mutation in SLC13A5', 'SLC13A5 deficiency', 'epileptic encephalopathy, early infantile, type 25', 'early infantile epileptic encephalopathy 25', 'SLC13A5 early infantile epileptic encephalopathy', 'developmental and epileptic encephalopathy 25, with amelogenesis imperfecta', 'epileptic encephalopathy, early infantile, 25']",0080453,615905,,C4014621,,,,,,,,
mondo:0014393,lymphatic malformation 4,"['LMPH1D', 'lymphedema, hereditary, 1D', 'lymphedema, hereditary, type 1D', 'hereditary lymphedema caused by mutation in VEGFC', 'VEGFC hereditary lymphedema']",0070209,615907,,C4014628,,,,,,,,
mondo:0014394,Diamond-Blackfan anemia 13,"['Diamond-Blackfan Anemia type 13', 'Diamond-Blackfan anemia 13', 'RPS29 Diamond-Blackfan anaemia', 'Diamond-Blackfan anemia caused by mutation in RPS29', 'Diamond-Blackfan Anaemia type 13', 'Diamond-Blackfan anaemia caused by mutation in RPS29', 'DBA13', 'RPS29 Diamond-Blackfan anemia']",0111889,615909,,C4014641,,,,,,,,
mondo:0014395,frontotemporal dementia and/or amyotrophic lateral sclerosis 2,"['frontotemporal dementia and/or amyotrophic lateral sclerosis type 2', 'frontotemporal dementia and/or amyotrophic lateral sclerosis 2', 'FTDALS2']",0060214,615911,,C4014648,,,,,,,,
mondo:0014396,dilated cardiomyopathy 1NN,"['RAF1 familial isolated dilated cardiomyopathy', 'cardiomyopathy, dilated, type 1Nn', 'dilated cardiomyopathy type 1NN', 'cardiomyopathy, dilated, 1NN', 'familial isolated dilated cardiomyopathy caused by mutation in RAF1', 'CMD1NN']",0110432,615916,,C4014656,,,,,,,,
mondo:0014397,combined oxidative phosphorylation defect type 20,"['combined oxidative phosphorylation deficiency type 20', 'COXPD20', 'combined oxidative phosphorylation deficiency 20', 'VARS2 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency caused by mutation in VARS2']",0111478,615917,420728,C4014660,"['-0.0361', '0.0286', '-0.003925', '-0.003353', '0.02557', '-0.04794', '-0.0007663', '0.03091', '-0.01942', '-0.01674', '-0.02094', '-0.01542', '0.01198', '-0.00266', '-0.01046', '-0.03696', '-0.00543', '-0.02829', '-0.02348', '-0.0726', '-0.002075', '-0.02621', '0.03693', '-0.01407', '0.005474', '-0.001017', '-0.0047', '-0.003695', '-0.002598', '-0.02914', '0.02385', '0.01217', '0.04346', '0.03217', '0.00787', '-0.03738', '-0.00978', '-0.013054', '-0.000742', '-0.03455', '0.02693', '-0.04343', '0.00978', '-0.004814', '-0.02138', '-0.02596', '0.00989', '0.02452', '-0.003332', '0.003706', '-0.01478', '-0.02666', '0.00179', '-0.006886', '-0.0319', '-0.010086', '0.04074', '-0.00917', '-0.04327', '0.01576', '0.0302', '0.010414', '0.01631', '-0.007057', '-0.002817', '0.00623', '0.03864', '0.03105', '-0.04858', '0.0413', '-0.0264', '0.0010195', '0.006752', '-0.02715', '0.02989', '0.02335', '0.00943', '-0.01246', '-0.013306', '-0.00934', '-0.001434', '-0.002205', '-0.01678', '0.01735', '-0.003832', '0.001637', '0.02213', '0.03903', '0.05832', '0.00597', '0.0239', '0.03278', '0.0014515', '0.013084', '0.07983', '0.02406', '0.03305', '-0.06055', '-0.008644', '0.02028']",,,,,,,
mondo:0014398,combined oxidative phosphorylation defect type 21,"['TARS2 combined oxidative phosphorylation deficiency', 'combined oxidative phosphorylation deficiency 21', 'combined oxidative phosphorylation deficiency type 21', 'combined oxidative phosphorylation deficiency caused by mutation in TARS2', 'COXPD21']",0111465,615918,420733,C4014668,"['-0.595', '0.2156', '0.2617', '-0.1969', '0.1375', '-0.363', '0.09955', '0.2076', '-0.595', '-0.06537', '-0.447', '-0.2438', '0.1262', '-0.6147', '0.0001593', '0.1571', '-0.2444', '-0.571', '-0.378', '-0.779', '0.3809', '-0.4648', '0.557', '-0.02002', '-0.3853', '-0.3154', '0.194', '0.0959', '-0.1906', '-0.1829', '0.126', '0.7026', '0.643', '-0.1184', '0.1047', '0.04575', '0.1036', '-0.1586', '0.07367', '-0.05594', '0.5537', '-0.483', '-0.293', '0.522', '-0.4004', '-0.0805', '0.06995', '0.2617', '-0.186', '-0.1388', '-0.4038', '-0.04108', '-0.1659', '0.075', '-0.818', '-0.2341', '0.05185', '0.0745', '-0.0967', '0.4255', '0.01886', '0.0643', '0.0847', '0.01492', '-0.837', '-0.01991', '0.4585', '0.3613', '-0.6157', '0.10205', '-0.0903', '0.2888', '-0.2456', '0.2947', '-0.178', '-0.3684', '0.295', '-0.1947', '-0.1954', '0.05', '-0.3726', '-0.01578', '0.1675', '0.7617', '-0.01363', '-0.175', '0.01787', '0.3801', '0.3386', '-0.08386', '0.874', '0.10236', '0.1913', '-0.3164', '0.6367', '0.4387', '0.1018', '-0.312', '0.3865', '0.229']",,0009032,,,,,
mondo:0014399,ataxia-telangiectasia-like disorder 2,"['ATLD2', 'ataxia-telangiectasia-like disorder type 2', 'PCNA-related progressive neurodegenerative photosensitivity syndrome', 'ataxia-telangiectasia-like disorder 2']",,615919,438134,C4014676,,,,,,,,
mondo:0014400,retinitis pigmentosa 70,"['retinitis pigmentosa 70', 'retinitis pigmentosa caused by mutation in PRPF4', 'retinitis pigmentosa type 70', 'RP70', 'PRPF4 retinitis pigmentosa']",0110392,615922,,C4014681,,,,,,H35.5,,
mondo:0014401,tall stature-scoliosis-macrodactyly of the great toes syndrome,"['ECDM', 'tall stature-scoliosis-macrodactyly of the halluces syndrome', 'epiphyseal chondrodysplasia, MIURA type', 'Miura type epiphyseal chondrodysplasia']",0070316,615923,329191,C4014690,"['0.2417', '0.2076', '0.1344', '-0.3066', '0.6133', '-1.131', '0.3674', '0.671', '-1.29', '-0.853', '0.7646', '0.2214', '-0.12396', '1.034', '-0.2273', '0.1913', '0.3625', '-0.4255', '-0.869', '-0.1456', '0.2118', '0.3857', '0.3623', '0.0498', '-0.2117', '-0.03717', '0.248', '0.2296', '0.2456', '0.01484', '0.6665', '-0.3206', '0.4175', '0.2211', '0.06793', '0.04666', '-0.637', '-1.087', '0.02496', '-0.02435', '0.279', '0.4688', '-0.4714', '0.2646', '0.4348', '0.2773', '-0.0936', '0.5557', '-0.04144', '-0.0812', '0.1946', '0.2145', '0.5615', '-0.1032', '-0.2103', '-0.2673', '-0.839', '0.3655', '-0.1045', '0.05728', '0.4397', '0.08167', '-0.1493', '0.6216', '-0.37', '0.3633', '-0.0899', '1.024', '-0.2097', '0.3247', '0.1659', '-0.03137', '0.2793', '-0.2627', '-0.539', '0.6055', '-0.3645', '0.482', '-0.2365', '-0.2642', '-0.02046', '-0.289', '-0.5254', '0.2046', '-0.1283', '-0.2234', '-0.0412', '-0.3962', '0.1136', '0.2305', '0.03235', '-0.4575', '-0.3835', '0.3918', '0.8027', '0.208', '0.3818', '-0.1927', '0.475', '0.1675']",,,,,,,
mondo:0014402,severe neurodegenerative syndrome with lipodystrophy,"['severe neurodegenerative syndrome due to BSCL2 deficiency', 'PELD', 'encephalopathy, progressive, with or without lipodystrophy']",,615924,363400,C4014700,"['-0.2537', '0.1912', '0.293', '-0.4548', '-0.1578', '-0.4924', '0.0981', '0.4436', '-0.4656', '0.09564', '-0.401', '-0.2184', '-0.1257', '-0.1859', '0.2477', '-0.1356', '0.2827', '-0.1427', '-0.2961', '-0.716', '0.181', '-0.2081', '0.00832', '0.01642', '0.1583', '0.09686', '0.06256', '-0.2386', '-0.1359', '-0.2764', '0.189', '0.1196', '0.442', '0.11646', '-0.000323', '-0.1041', '-0.2935', '-0.07574', '-0.3994', '-0.139', '0.1013', '-0.1826', '-0.2095', '0.342', '0.1652', '-0.2086', '-0.1927', '0.2883', '-0.2115', '0.087', '-0.2854', '0.5195', '-0.063', '-0.2141', '0.1825', '0.04147', '0.02168', '-0.4307', '-0.3645', '0.2003', '0.0665', '0.02858', '0.2192', '-0.02835', '-0.4255', '0.001131', '0.266', '0.339', '-0.183', '0.1523', '-0.4265', '0.12115', '0.03079', '-0.1599', '0.1953', '-0.1046', '0.235', '-0.11456', '-0.1517', '-0.2021', '0.0798', '-0.0757', '-0.07', '0.4695', '0.07623', '0.0912', '-0.11316', '0.28', '0.4534', '0.2219', '0.4229', '0.43', '-0.03247', '0.05634', '0.2217', '0.1909', '0.3726', '-0.0864', '0.2722', '0.233']",,,,,,,
mondo:0014403,short stature due to GHSR deficiency,"['short stature due to growth hormone secretagogue receptor deficiency', 'GHDP', 'ghrelin receptor deficiency', 'growth hormone deficiency, isolated partial']",,615925,314811,,"['-1.039', '0.1652', '0.3198', '-0.2351', '0.3877', '0.03204', '0.3276', '0.548', '-0.4995', '-0.3838', '0.04788', '-0.0199', '-0.1945', '0.1514', '0.0315', '-0.2198', '0.1587', '-0.0395', '-0.643', '-0.6963', '0.2014', '-0.4133', '0.1058', '-0.701', '0.3384', '-0.10156', '-0.3625', '-0.2837', '0.1421', '-0.218', '0.6143', '0.0498', '0.2167', '-0.03143', '-0.2395', '-0.2617', '0.002926', '-0.192', '-0.2354', '0.0563', '0.2913', '-0.089', '0.00844', '-0.02222', '0.09924', '-0.1122', '0.532', '-0.255', '0.02986', '-0.126', '0.2134', '-0.145', '0.1335', '0.332', '-0.466', '0.043', '-0.1703', '-0.4614', '-0.1995', '0.568', '0.2068', '0.149', '-0.2517', '-0.181', '0.0504', '0.07837', '0.0339', '0.3027', '-0.513', '0.1437', '-0.161', '0.2634', '0.465', '0.1238', '-0.02083', '0.1404', '-0.1948', '0.1692', '-0.3306', '-0.104', '0.332', '0.3464', '-0.2395', '0.04492', '-0.02892', '0.4673', '0.2197', '0.1948', '0.8853', '0.1076', '0.05386', '0.536', '-0.1142', '-0.3616', '1.048', '-0.08496', '0.283', '-0.387', '0.3105', '0.3381']",,,,,,,
mondo:0014404,Webb-Dattani syndrome,"['WEDAS', 'WEBB-Dattani syndrome', 'hypothalamo-pituitary-frontotemporal hypoplasia with visual and renal anomalies', 'hypothalamic insufficiency-secondary microcephaly-visual impairment-urinary anomalies syndrome', 'Webb-Dattani syndrome']",,615926,370006,C4014708,"['-0.0676', '0.0687', '0.04205', '-0.0293', '0.02422', '-0.05545', '0.01221', '0.08136', '-0.07605', '-0.06207', '-0.0676', '-0.03772', '0.006348', '0.03784', '-0.05463', '-0.03445', '-0.01895', '-0.02553', '-0.0634', '-0.1514', '-0.002375', '-0.03558', '0.07245', '-0.02505', '0.01884', '-0.006866', '-0.01443', '-0.007458', '0.02872', '-0.04874', '0.0852', '-0.0413', '0.10913', '0.05072', '0.05634', '-0.01932', '0.01689', '-0.02061', '-0.01756', '-0.0811', '0.05423', '-0.03995', '0.04373', '-0.02692', '-0.000859', '-0.096', '0.0101', '0.047', '-0.02039', '0.03244', '-0.03427', '0.01575', '0.00439', '0.01431', '-0.03928', '0.00501', '0.05032', '-0.02667', '-0.11237', '0.04483', '0.01654', '0.0459', '-0.03455', '0.03372', '-0.003845', '0.00357', '0.08014', '0.1051', '-0.0822', '0.073', '-0.07697', '0.05002', '0.0244', '-0.0386', '0.004997', '0.00506', '0.04004', '-0.02295', '-0.04184', '-0.064', '-0.0168', '0.02478', '-0.0183', '0.0737', '-0.01875', '0.02924', '0.001004', '0.07874', '0.09247', '0.02187', '0.02406', '0.0555', '-0.01825', '0.01582', '0.1545', '0.02542', '0.0796', '-0.09436', '0.02893', '0.04193']",,,,,,,
mondo:0014405,STING-associated vasculopathy with onset in infancy,"['SAVI', 'STING-associated vasculopathy, infantile-onset']",0111457,615934,425120,C4040879,,,,,279.8,,,
mondo:0014406,pancreatic agenesis 2,"['pancreatic agenesis 2', 'pancreatic agenesis type 2', 'pancreatic agenesis caused by mutation in PTF1A', 'PAGEN2', 'pancreatic hypoplasia, congenital 2', 'PTF1A pancreatic agenesis']",,615935,,C4014737,,,,,,,,
mondo:0014407,megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2,"['megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 2', 'AKT3 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome', 'MPPH2', 'megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in AKT3', 'megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 2']",,615937,,C4014738,,,,,,,,
mondo:0014408,megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3,"['CCND2 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome', 'MPPH3', 'megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in CCND2', 'megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3', 'megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 3']",,615938,,C4014742,,,,,,,,
mondo:0014409,"intellectual disability, autosomal recessive 44","['intellectual disability, autosomal recessive 44', 'MRT44', 'METTL23 autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive 44', 'mental retardation, autosomal recessive type 44', 'intellectual disability, autosomal recessive type 44', 'autosomal recessive non-syndromic intellectual disability caused by mutation in METTL23']",0081208,615942,,C4014745,,,,,,,,
mondo:0014410,spinocerebellar ataxia type 37,"['SCA37', 'spinocerebellar ataxia with altered vertical eye movements', 'spinocerebellar ataxia 37']",0050984,615945,363710,C4304821,"['-0.0621', '-0.09064', '-0.275', '0.1388', '-0.1082', '-0.7856', '0.248', '0.3572', '-0.6616', '-0.894', '0.04147', '0.11584', '0.04782', '0.2399', '0.5503', '-0.2834', '-0.1285', '-0.2319', '0.1141', '-0.857', '-0.2559', '-0.4814', '0.2957', '-0.587', '-0.0001069', '-0.6416', '-0.405', '0.1898', '0.01279', '-0.902', '0.3132', '0.457', '-0.561', '-0.3008', '0.3145', '0.1599', '0.1606', '0.1617', '0.5703', '0.4084', '0.4524', '0.1515', '-0.3174', '0.538', '0.53', '-0.618', '-0.01504', '0.04895', '0.296', '-0.284', '-0.2413', '0.0729', '0.0938', '-0.553', '-0.05484', '-0.751', '0.4277', '0.6274', '-0.07166', '0.5054', '-0.4778', '0.3687', '0.0319', '-0.2031', '-0.3904', '0.394', '0.3684', '0.42', '-0.574', '0.3213', '0.636', '0.416', '-0.1606', '-0.7715', '0.5474', '0.2788', '0.1316', '0.01717', '0.03098', '0.431', '-0.08185', '-0.7827', '0.4731', '0.679', '-0.2983', '-0.6914', '0.12335', '0.12494', '0.595', '0.3', '0.304', '0.5835', '-0.10425', '-0.0368', '0.774', '0.8857', '0.3533', '0.4185', '-0.133', '-0.00418']",,,,,,,
mondo:0014411,"myopia 24, autosomal dominant","['MYP24', 'myopia 24, autosomal dominant']",,615946,,C4014762,,,,,,,,
mondo:0014412,"hyperlipoproteinemia, type 1D","['GPIHBP1 familial hyperlipidemia', 'hyperlipoproteinemia, type ID', 'familial hyperlipidemia caused by mutation in GPIHBP1']",0111420,615947,535458,C4014767,,,,,,,,
mondo:0014413,orofaciodigital syndrome type 14,"['OFD14', 'orofaciodigital syndrome caused by mutation in C2CD3', 'oral-facial-digital syndrome type 14', 'microcephaly-cerebral malformation-orofaciodigital syndrome', 'orofaciodigital syndrome type 14', 'orofaciodigital syndrome 14', 'orofaciodigital syndrome XIV', 'C2CD3 orofaciodigital syndrome']",,615948,434179,C4014780,,,,,,,,
mondo:0014414,STAT3-related early-onset multisystem autoimmune disease,"['autoimmune disease, multisystem, infantile-onset, 1', 'autoimmune disease, multisystem, infantile-onset', 'ADMIO1', 'ADMIO']",,615952,438159,C4014795,,,,,,,,
mondo:0014415,"kallikrein, decreased urinary activity of","['kallikrein, decreased urinary activity of']",,615953,,,"['-0.0736', '0.09406', '-0.004448', '-0.01717', '-0.003304', '-0.05374', '0.010025', '0.1648', '-0.0693', '-0.000416', '-0.02133', '-0.05215', '-0.00683', '0.03812', '-0.1114', '-0.0345', '0.02951', '-0.04184', '-0.081', '-0.1813', '0.00533', '-0.05606', '0.0828', '-0.02724', '0.04752', '-0.02478', '0.01307', '-0.01926', '-0.04584', '-0.0187', '0.08203', '-0.05887', '0.1251', '0.03748', '-0.02087', '-0.0585', '-0.03296', '0.01027', '0.005283', '-0.1131', '0.05084', '-0.06198', '0.03096', '0.002237', '-0.02013', '-0.1082', '0.03738', '0.03967', '0.05734', '0.0969', '-0.0649', '-0.003628', '0.03026', '-0.0532', '-0.0493', '0.01645', '0.11066', '-0.05966', '-0.1398', '-0.01797', '0.0183', '0.05106', '0.01138', '0.0276', '0.003284', '0.06836', '0.0883', '0.04926', '-0.0878', '0.0882', '-0.05893', '0.05978', '0.01377', '-0.03577', '0.0672', '0.0598', '0.05643', '0.006725', '-0.06525', '-0.04715', '0.01022', '0.004498', '0.05585', '0.0768', '-0.003458', '0.01363', '0.0191', '0.0558', '0.145', '-0.01833', '0.008385', '0.0865', '-0.03915', '0.03845', '0.1882', '0.11926', '0.0323', '-0.1284', '-0.0367', '0.06433']",,,C563653,,,,
mondo:0014416,ACTH-independent macronodular adrenal hyperplasia 2,"['ARMC5 Cushing syndrome due to macronodular adrenal hyperplasia', 'Cushing syndrome due to macronodular adrenal hyperplasia caused by mutation in ARMC5', 'ACTH-independent macronodular adrenal hyperplasia 2, autosomal dominant, somatic mutation', 'primary macronodular adrenal hyperplasia', 'AIMAH2', 'ACTH-independent macronodular adrenal hyperplasia type 2', 'ACTH-independent macronodular adrenal hyperplasia 2']",0111624,615954,,C4014803,,,,,,,,
mondo:0014417,spinocerebellar ataxia type 38,"['spinocerebellar ataxia type 38', 'SCA38', 'spinocerebellar ataxia 38']",0050985,615957,423296,C4518337,"['-0.2368', '-0.1387', '0.02751', '0.05054', '-0.2979', '-1.023', '0.2004', '-0.12463', '-0.7827', '-0.8687', '-0.09314', '0.2744', '-0.2025', '0.298', '0.4724', '-0.2156', '-0.0991', '-0.3113', '0.1366', '-0.943', '0.02103', '-0.2406', '0.1693', '-0.597', '0.3545', '-0.5205', '-0.3247', '0.1759', '-0.1625', '-0.9644', '0.12256', '0.489', '-0.6133', '-0.001075', '0.4504', '0.07715', '-0.1929', '0.1471', '0.573', '0.2537', '0.5176', '0.2096', '-0.418', '0.5845', '0.4656', '-0.6626', '0.1378', '0.59', '0.3088', '-0.002333', '-0.2432', '0.199', '-0.2056', '-0.4075', '0.01345', '-0.9043', '0.4414', '0.6978', '-0.03546', '0.6265', '-0.616', '0.26', '0.2605', '-0.1515', '-0.5503', '0.606', '0.2296', '0.4976', '-0.612', '0.4412', '0.8438', '0.744', '0.0578', '-0.798', '0.7974', '0.3113', '0.1426', '0.3406', '0.0704', '0.628', '-0.496', '-1.007', '0.43', '0.9233', '-0.2222', '-0.482', '0.2993', '-0.096', '0.4424', '0.56', '0.4934', '0.4175', '0.2084', '0.1755', '1.14', '0.9844', '0.3142', '0.601', '-0.3923', '0.003029']",,0009056,,,,,
mondo:0014418,"myopathy, centronuclear, 5","['autosomal recessive centronuclear myopathy caused by mutation in SPEG', 'centronuclear myopathy 5', 'myopathy, centronuclear, type 5', 'myopathy, centronuclear, 5', 'SPEG autosomal recessive centronuclear myopathy', 'CNM5']",0111222,615959,,C4014814,,,,,,,,
mondo:0014419,ataxia - intellectual disability - oculomotor apraxia - cerebellar cysts syndrome,"['PTBHS', 'PORETTI-Boltshauser syndrome', 'Poretti-Boltshauser syndrome']",,615960,370022,C4014821,"['-0.1842', '-0.3843', '-0.02118', '-0.02916', '-0.0782', '-0.881', '-0.01415', '-0.04526', '-0.6377', '-0.882', '-0.1442', '0.1615', '-0.1131', '-0.0636', '0.6177', '-0.2734', '-0.2015', '-0.1688', '0.2344', '-0.9976', '0.1129', '0.001163', '0.09064', '-0.5845', '0.4421', '-0.4302', '-0.4016', '0.0941', '-0.0738', '-0.8965', '-0.00677', '0.339', '-0.4514', '-0.1703', '0.5366', '0.2563', '-0.1655', '0.01523', '0.598', '0.386', '0.44', '0.626', '-0.4888', '0.416', '0.4019', '-0.4138', '0.2886', '0.5884', '0.4585', '-0.1836', '-0.126', '0.2542', '-0.1968', '-0.4438', '-0.1936', '-0.694', '0.2042', '0.5156', '-0.2428', '0.6846', '-0.3271', '0.406', '0.2437', '-0.0717', '-0.537', '0.567', '0.363', '0.6104', '-0.3516', '0.3896', '0.8315', '0.3708', '-0.1549', '-0.6406', '0.623', '0.3315', '0.1865', '0.0925', '-0.0807', '0.5225', '-0.364', '-0.7793', '0.2593', '0.98', '-0.484', '-0.689', '0.1747', '0.253', '0.556', '0.847', '0.4307', '0.5845', '0.10297', '0.04492', '1.192', '0.775', '0.5054', '0.535', '-0.2216', '-0.1959']",,,,,,,
mondo:0014420,short stature due to primary acid-labile subunit deficiency,"['acid-labile SUBUNIT deficiency', 'ACLSD', 'acid-labile subunit, deficiency of']",,615961,140941,C3900122,"['-0.515', '-0.0616', '0.3037', '-0.5645', '0.4822', '0.009575', '0.1746', '0.8564', '-0.295', '-0.814', '-0.2002', '0.5137', '-0.136', '-0.2556', '-0.04617', '0.07635', '1.0625', '0.255', '-0.534', '-0.649', '0.113', '-0.7666', '-0.01741', '-0.1274', '0.2373', '0.514', '0.1128', '-0.4546', '0.01779', '-0.1616', '0.3772', '-0.2393', '0.337', '0.316', '-0.447', '-0.495', '-0.01884', '-0.234', '0.06232', '0.04846', '0.1663', '-0.2861', '0.06104', '0.0698', '-0.03125', '-0.564', '0.2031', '0.07574', '-0.04684', '-0.0701', '0.2695', '-0.663', '-0.536', '0.7666', '-0.4797', '0.06158', '0.179', '-0.604', '-0.4214', '0.2878', '0.05072', '0.332', '0.1172', '-0.551', '0.1562', '-0.193', '-0.3328', '0.2622', '-0.71', '-0.545', '-0.4443', '0.1268', '0.1953', '-0.265', '0.528', '0.3772', '0.2196', '0.334', '0.00892', '0.1368', '0.2275', '0.6943', '0.03497', '0.0395', '-0.09143', '0.09454', '0.3264', '0.7017', '0.7676', '0.1038', '0.1433', '0.4263', '-0.335', '-0.618', '1.013', '0.7495', '0.1508', '-0.981', '0.4512', '-0.0353']",,,,,,,
mondo:0014421,glucocorticoid resistance,"['cortisol resistance from glucocorticoid receptor defect', 'Grl deficiency', 'glucocorticoid receptor deficiency', 'glucocorticoid resistance, generalised', 'glucocorticoid resistance, generalized', 'GCCR', 'Gcr deficiency', 'Gccr deficiency']",,615962,786,C1841972,"['-0.5723', '0.1859', '0.1294', '-0.3613', '0.3594', '-0.2742', '0.004208', '0.3586', '-0.05606', '-0.2281', '-0.03674', '0.0115', '0.1934', '0.2996', '-0.1142', '-0.03204', '0.226', '0.239', '-0.266', '-0.344', '-0.3367', '-0.3696', '0.576', '-0.2257', '0.3635', '0.431', '0.3564', '-0.1776', '0.11993', '-0.2118', '0.65', '-0.0695', '0.508', '0.1187', '-0.10706', '-0.2893', '0.2299', '-0.10254', '-0.308', '-0.1967', '0.305', '-0.0466', '0.175', '-0.1265', '-0.0917', '-0.533', '0.01727', '-0.05365', '0.1656', '0.4714', '0.1458', '-0.1643', '0.0971', '0.2045', '-0.0709', '0.256', '0.581', '-0.5317', '-0.149', '0.06335', '0.0808', '0.2556', '-0.12195', '-0.0857', '0.1844', '0.2474', '-0.07556', '0.2573', '-0.1661', '0.0894', '-0.1393', '-0.2356', '0.02548', '-0.091', '0.0772', '-0.207', '0.329', '0.1902', '-0.10754', '-0.2344', '0.2253', '0.281', '0.4468', '-0.3894', '0.169', '0.1805', '0.12384', '-0.1459', '0.5034', '-0.0632', '-0.0309', '0.296', '-0.11426', '-0.1865', '0.715', '-0.02', '0.2389', '-0.1697', '-0.0679', '0.3557']",,,C564221,,,,
mondo:0014422,vesicoureteral reflux 8,"['vesicoureteral reflux type 8', 'TNXB vesicoureteral reflux (disease)', 'VUR8', 'vesicoureteral reflux 8']",,615963,,C4014831,,,,,,,,
mondo:0014423,severe combined immunodeficiency due to DNA-PKcs deficiency,"['SCID due to DNA-PKcs deficiency', 'IMD26', 'immunodeficiency 26, with or without neurologic abnormalities', 'immunodeficiency 26 with or without neurologic abnormalities']",0111961,615966,317425,C4014833,"['-0.37', '0.3042', '0.08466', '-0.6084', '0.1744', '-0.2534', '0.3677', '0.08624', '-0.00511', '-0.341', '0.1451', '0.003357', '-0.5537', '0.0689', '-0.596', '-0.1971', '0.388', '0.2266', '-0.06192', '-0.506', '-0.3977', '-0.3936', '0.6187', '-0.385', '0.2969', '0.1545', '0.1869', '0.03662', '-0.2708', '-0.2395', '0.0484', '0.782', '0.826', '-0.1918', '0.02087', '-0.3281', '-0.5874', '0.02434', '-0.6494', '-0.2228', '-0.1958', '-0.4424', '0.0364', '-0.4421', '-0.3328', '-0.1721', '-0.0737', '-0.2588', '0.6196', '0.1094', '0.0884', '-0.302', '0.42', '-0.264', '-0.4932', '-0.1019', '-0.1395', '-0.4177', '-0.5176', '-0.01593', '-0.2113', '0.2864', '0.2078', '-0.11395', '0.3816', '0.082', '0.559', '0.387', '-0.2495', '0.43', '-0.4478', '-0.1465', '-0.12354', '-0.4773', '0.2751', '0.2296', '-0.01299', '-0.1605', '0.2898', '0.4106', '-0.0799', '-0.1666', '-0.3782', '-0.2025', '-0.0478', '-0.3845', '0.52', '0.5566', '0.7344', '-0.2769', '0.3193', '0.5547', '-0.2029', '-0.1755', '0.5996', '0.9893', '0.05353', '-0.8247', '-0.1011', '0.11224']",,,,,,,
mondo:0014426,nanophthalmos 4,"['NNO4', 'TMEM98 nanophthalmia', 'nanophthalmos 4', 'nanophthalmos type 4', 'nanophthalmia caused by mutation in TMEM98', 'Nanophthalmia 4']",,615972,,C4014848,,,,,,,,
mondo:0014427,cone-rod dystrophy 20,"['cone-rod dystrophy type 20', 'POC1B cone-rod dystrophy', 'cone-rod dystrophy 20', 'cone-rod dystrophy caused by mutation in POC1B', 'CORD20']",0111026,615973,,C4014856,,,,,,,,
mondo:0014428,autosomal recessive nonsyndromic hearing loss 102,"['EPS8 autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 102', 'autosomal recessive deafness 102', 'autosomal recessive nonsyndromic deafness caused by mutation in EPS8', 'autosomal recessive nonsyndromic deafness 102', 'DFNB102', 'deafness, autosomal recessive 102', 'deafness, autosomal recessive type 102']",0110463,615974,,C3892050,,,,,,,,
mondo:0014429,autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial IFNgammaR1 deficiency,"['autosomal dominant MSMD due to partial interferon gamma receptor 1 deficiency', 'IFNGR1 autosomal dominant mendelian susceptibility to mycobacterial diseases due to a partial deficiency', 'IMD27B', 'immunodeficiency 27B, mycobacteriosis, AD', 'autosomal dominant MSMD due to partial IFNgammaR1 deficiency', 'immunodeficiency type 27B', 'immunodeficiency 27B, Mycobacteriosis, autosomal dominant', 'immunodeficiency 27B', 'autosomal dominant mendelian susceptibility to mycobacterial diseases due to partial interferon gamma receptor 1 deficiency', 'IFNGR1 deficiency, autosomal dominant']",0111956,615978,319581,C4014863,"['0.1805', '0.355', '0.01487', '-0.5557', '0.23', '-0.4238', '0.577', '0.0702', '0.3447', '-0.658', '0.2375', '0.318', '-0.4238', '0.2059', '0.57', '-0.1407', '-0.07104', '-0.3938', '-0.511', '-0.5806', '-0.05664', '-0.03323', '0.585', '-0.3716', '-0.3687', '0.4512', '-0.8423', '-0.10754', '-0.0705', '-0.5376', '-0.216', '-0.1726', '0.5063', '0.3704', '0.1989', '-0.627', '-0.4143', '-0.499', '-0.7197', '-0.1245', '-0.1211', '-0.3718', '0.4438', '-0.1892', '-0.362', '-0.356', '-0.3667', '-0.4954', '0.06323', '0.549', '0.3125', '-0.2434', '0.306', '-0.2288', '-0.3264', '0.07465', '0.718', '-0.534', '-0.1334', '0.736', '0.1393', '0.7354', '0.16', '0.069', '1.088', '0.2112', '0.1327', '0.1482', '-0.07886', '0.79', '0.07214', '-0.2737', '0.0898', '-0.6943', '0.864', '0.6143', '0.3723', '0.05057', '-0.2542', '0.3618', '-0.6733', '0.6455', '0.546', '0.4622', '0.02046', '0.2192', '0.7144', '0.6836', '0.698', '0.0929', '0.5044', '0.1902', '-0.2822', '-0.4548', '0.6636', '0.728', '0.3354', '-0.6274', '-0.03888', '-0.4502']",,,,,,,
mondo:0014430,"intellectual disability, autosomal recessive 45","['MRT45', 'FBXO31 autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive type 45', 'intellectual disability, autosomal recessive 45', 'mental retardation, autosomal recessive 45', 'autosomal recessive non-syndromic intellectual disability caused by mutation in FBXO31', 'intellectual disability, autosomal recessive type 45']",0081209,615979,,C4014864,,,,,,,,
mondo:0014431,LIPE-related familial partial lipodystrophy,"['lipodystrophy, familial partial, associated with Lipe mutations', 'familial partial lipodystrophy associated with LIPE mutations', 'LIPE-related FPLD', 'lipodystrophy, familial partial, type 6', 'familial partial lipodystrophy type 6', 'FPLD6']",0070206,615980,435660,C4014869,,,,,,,,
mondo:0014432,Bardet-Biedl syndrome 2,"['BBS2', 'Bardet-Biedl syndrome 2', 'BBS2 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome', 'Bardet-Biedl syndrome type 2', 'Bardet-Biedl syndrome caused by mutation in BBS2', 'BBS']",0110124,615981,,C2936863,,,,C537910,,,,
mondo:0014433,Bardet-Biedl syndrome 4,"['Bardet-Biedl syndrome 4', 'Bardet-Biedl syndrome type 4', 'BBS4']",0110126,615982,,C2936864,"['-0.03857', '0.0944', '-0.001237', '0.001454', '0.02806', '-0.1185', '-0.00766', '0.1038', '-0.10065', '-0.05847', '-0.023', '-0.005722', '0.02745', '0.01141', '1.895e-05', '-0.0714', '-0.00897', '-0.05835', '0.010086', '-0.1445', '0.003641', '-0.00846', '0.0995', '-0.0596', '0.05167', '0.01942', '-0.05426', '-0.011566', '0.04135', '-0.051', '0.094', '-0.01349', '0.1036', '0.05975', '0.05054', '-0.0887', '-0.00811', '-0.05692', '-0.01051', '-0.0535', '0.03574', '-0.10645', '0.00924', '-0.06125', '-0.03156', '-0.1214', '-0.0413', '0.07385', '4.9e-05', '-0.007557', '-0.0227', '-0.01718', '-0.02905', '-0.01145', '-0.04938', '-0.06866', '0.1293', '-0.03075', '-0.12384', '0.01358', '0.05695', '0.0396', '0.01727', '0.0584', '0.001742', '0.02776', '0.0803', '0.052', '-0.0954', '0.1073', '-0.1127', '0.010376', '0.02455', '-0.0772', '0.08264', '0.04364', '-0.0428', '-0.02834', '-0.1029', '-0.0434', '0.04102', '0.02295', '-0.0441', '0.1114', '-0.000336', '-0.02979', '0.06775', '0.1345', '0.0989', '0.04495', '0.03677', '0.04907', '0.0264', '-0.02391', '0.2041', '0.01828', '0.1033', '-0.1732', '-0.00397', '-0.002033']",,0009024,C537912,,,,
mondo:0014434,Bardet-Biedl syndrome 5,"['BBS5', 'BBS5 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome 5', 'Bardet-Biedl syndrome caused by mutation in BBS5', 'Bardet-Biedl syndrome type 5']",0110127,615983,,C3892039,"['-0.174', '0.1852', '-0.02846', '0.0854', '0.04346', '-0.2491', '-0.05576', '0.1525', '-0.2847', '-0.1335', '-0.01213', '-0.01619', '-0.001113', '0.02869', '0.1277', '-0.1742', '-0.1102', '-0.0415', '-0.07074', '-0.2295', '0.108', '-0.04532', '0.1145', '-0.08545', '0.1549', '0.0651', '-0.0701', '0.0464', '0.0671', '-0.01765', '0.134', '0.02504', '0.1587', '0.08514', '0.1527', '-0.11145', '0.03165', '-0.1009', '0.04465', '-0.1494', '0.0956', '-0.1857', '0.0893', '-0.098', '-0.05997', '-0.2285', '-0.01971', '0.0867', '0.09406', '-0.04288', '-0.01232', '-0.0707', '0.02583', '0.03168', '-0.0972', '-0.1495', '0.356', '0.02336', '-0.2627', '0.04077', '0.09143', '0.0805', '0.1475', '0.01782', '0.065', '0.147', '0.177', '0.01033', '-0.2021', '0.1863', '-0.2573', '-0.0368', '0.06134', '-0.1681', '0.1895', '0.0401', '-0.04797', '0.007214', '-0.1685', '-0.006275', '0.01813', '0.005604', '-0.0806', '0.136', '-0.0242', '-0.1818', '0.19', '0.2947', '0.171', '0.1566', '0.09546', '0.002102', '0.05966', '-0.141', '0.438', '0.1058', '0.209', '-0.3738', '0.02403', '-0.04562']",,0009025,,,,,
mondo:0014435,Bardet-Biedl syndrome 7,"['Bardet-Biedl syndrome type 7', 'Bardet-Biedl syndrome caused by mutation in BBS7', 'BBS7 Bardet-Biedl syndrome', 'BBS7', 'Bardet-Biedl syndrome 7']",0110129,615984,,C1859565,"['-0.167', '0.1993', '-0.0286', '0.07184', '0.052', '-0.2788', '-0.05487', '0.1588', '-0.2786', '-0.1177', '-0.02197', '-0.04333', '-0.01042', '0.05423', '0.1564', '-0.1648', '-0.09143', '-0.03308', '-0.05844', '-0.2485', '0.1221', '-0.06244', '0.10406', '-0.09467', '0.1594', '0.03378', '-0.0404', '0.04742', '0.0864', '-0.05353', '0.1313', '0.04053', '0.1687', '0.10315', '0.149', '-0.0932', '0.05008', '-0.1333', '0.0348', '-0.1434', '0.08844', '-0.1562', '0.08124', '-0.0446', '-0.05258', '-0.2484', '0.001171', '0.0413', '0.1004', '-0.03568', '-0.01303', '-0.09674', '0.02126', '0.04965', '-0.082', '-0.1621', '0.3271', '0.0211', '-0.2537', '0.077', '0.09766', '0.10205', '0.1371', '0.03418', '0.10406', '0.1439', '0.1628', '0.01263', '-0.2035', '0.2109', '-0.2969', '-0.02348', '0.0661', '-0.1588', '0.148', '-0.01141', '-0.04663', '0.02217', '-0.1278', '0.0209', '0.02873', '0.012856', '-0.1001', '0.131', '-0.03403', '-0.1692', '0.1981', '0.2632', '0.1885', '0.1273', '0.1036', '0.00927', '0.04575', '-0.10626', '0.4294', '0.05414', '0.2025', '-0.3809', '0.0005608', '-0.0364']",,0009026,C565916,,,,
mondo:0014436,Bardet-Biedl syndrome 8,"['TTC8 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome type 8', 'Bardet-Biedl syndrome 8', 'BBS8', 'Bardet-Biedl syndrome caused by mutation in TTC8']",0110130,615985,,C1859566,,,,C565917,,,,
mondo:0014437,Bardet-Biedl syndrome 9,"['BBS9', 'BBS9 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome 9', 'Bardet-Biedl syndrome caused by mutation in BBS9', 'Bardet-Biedl syndrome type 9']",0110131,615986,,C1859567,"['-0.2015', '0.1776', '-0.05002', '0.0399', '0.0006576', '-0.2788', '-0.05414', '0.1036', '-0.2388', '-0.1261', '-0.0055', '-0.04694', '-0.002125', '0.03912', '0.10767', '-0.1537', '-0.0928', '-0.05447', '-0.0727', '-0.2399', '0.11597', '-0.06323', '0.09204', '-0.07825', '0.1594', '0.02663', '-0.05475', '0.0275', '0.0947', '-0.02748', '0.10394', '0.0324', '0.1619', '0.084', '0.1771', '-0.1068', '0.03574', '-0.0973', '0.003277', '-0.1804', '0.1048', '-0.172', '0.0796', '-0.05075', '-0.0746', '-0.2598', '-0.005516', '0.05072', '0.10315', '-0.03946', '-0.0002428', '-0.07263', '0.01473', '0.05386', '-0.1022', '-0.153', '0.3357', '0.02829', '-0.2688', '0.07385', '0.0707', '0.08356', '0.1307', '0.0353', '0.08167', '0.1548', '0.1404', '-0.002298', '-0.1935', '0.2131', '-0.3015', '-0.01213', '0.07336', '-0.1162', '0.168', '0.02995', '-0.04388', '0.01671', '-0.1231', '0.01303', '0.01147', '0.000152', '-0.09076', '0.1293', '-0.04254', '-0.1667', '0.2108', '0.3071', '0.1808', '0.137', '0.0811', '-0.02408', '0.06113', '-0.1173', '0.4114', '0.0712', '0.2233', '-0.3862', '0.008064', '-0.0346']",,0009027,C565918,,,,
mondo:0014438,Bardet-Biedl syndrome 10,"['Bardet-Biedl syndrome caused by mutation in BBS10', 'Bardet-Biedl syndrome 10', 'BBS10', 'Bardet-Biedl syndrome type 10', 'BBS10 Bardet-Biedl syndrome']",0110132,615987,,C1859568,"['-0.171', '0.174', '-0.0464', '0.0141', '0.04678', '-0.2153', '-0.0285', '0.1774', '-0.2876', '-0.152', '-0.0004041', '-0.0004332', '-0.02608', '0.006676', '0.0998', '-0.1934', '-0.0634', '-0.03595', '-0.02867', '-0.2378', '0.1489', '-0.0811', '0.10675', '-0.1128', '0.1346', '0.04727', '-0.06287', '0.03473', '0.0955', '-0.007553', '0.1038', '0.01952', '0.1604', '0.09143', '0.1448', '-0.10443', '0.00337', '-0.1231', '0.006485', '-0.11444', '0.1234', '-0.1779', '0.06866', '-0.07935', '-0.04224', '-0.217', '-0.0239', '0.0626', '0.1149', '-0.01125', '-0.01277', '-0.0754', '0.02463', '0.01765', '-0.0916', '-0.1672', '0.3333', '-0.01688', '-0.2202', '0.02155', '0.1263', '0.0995', '0.12036', '0.006874', '0.06976', '0.11475', '0.171', '0.03207', '-0.2175', '0.2063', '-0.2524', '-0.003372', '0.0864', '-0.1334', '0.172', '0.00891', '-0.03041', '0.03625', '-0.152', '-0.0321', '0.00786', '0.006794', '-0.0635', '0.12195', '-0.01918', '-0.1635', '0.1802', '0.2751', '0.194', '0.162', '0.0848', '0.00952', '0.04037', '-0.08545', '0.4138', '0.0718', '0.1996', '-0.359', '0.01965', '-0.00808']",,0009022,C565919,,,,
mondo:0014439,Bardet-Biedl syndrome 11,"['BBS11', 'Bardet-Biedl syndrome caused by mutation in TRIM32', 'Bardet-Biedl syndrome type 11', 'TRIM32 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome 11']",0110133,615988,,C1859569,,,,C565920,,,,
mondo:0014440,Bardet-Biedl syndrome 12,"['Bardet-Biedl syndrome 12', 'BBS12 Bardet-Biedl syndrome', 'BBS12', 'Bardet-Biedl syndrome caused by mutation in BBS12', 'Bardet-Biedl syndrome type 12']",0110134,615989,,C1859570,"['-0.185', '0.1592', '-0.0368', '0.0418', '0.0458', '-0.2764', '-0.0335', '0.1537', '-0.2913', '-0.1395', '-0.02722', '-0.05972', '-0.00866', '0.0641', '0.11926', '-0.171', '-0.09326', '-0.04163', '-0.05035', '-0.259', '0.1489', '-0.0695', '0.1301', '-0.0797', '0.1553', '0.05542', '-0.04944', '0.04996', '0.0757', '-0.03738', '0.1526', '0.02106', '0.1599', '0.0945', '0.1597', '-0.079', '0.00913', '-0.1092', '0.01556', '-0.1329', '0.1145', '-0.1626', '0.0595', '-0.0646', '-0.04822', '-0.2407', '-0.006054', '0.0359', '0.142', '-0.0359', '-0.00596', '-0.06085', '0.0458', '0.0383', '-0.08673', '-0.1564', '0.3132', '0.03085', '-0.229', '0.03827', '0.08484', '0.0699', '0.1193', '0.02025', '0.0822', '0.1584', '0.1469', '0.02184', '-0.1892', '0.1957', '-0.2805', '-0.01334', '0.067', '-0.1292', '0.1365', '0.01872', '-0.03427', '0.02046', '-0.128', '-0.02441', '-0.00463', '-0.01232', '-0.0854', '0.1388', '-0.02415', '-0.1484', '0.2054', '0.249', '0.1686', '0.1652', '0.0844', '0.02104', '0.05374', '-0.0841', '0.409', '0.1023', '0.2017', '-0.3562', '0.0205', '-0.013016']",,0009023,C565921,,,,
mondo:0014441,Bardet-Biedl syndrome 13,"['Bardet-Biedl syndrome caused by mutation in MKS1', 'BBS13', 'Bardet-Biedl syndrome type 13', 'Bardet-Biedl syndrome 13', 'MKS1 Bardet-Biedl syndrome']",0110135,615990,,C2673873,,,,C567140,,,,
mondo:0014442,Bardet-Biedl syndrome 14,"['BBS14', 'Bardet-Biedl syndrome 14, modifier of', 'Bardet-Biedl syndrome type 14', 'Bardet-Biedl syndrome 14']",0110136,615991,,C2673874,,,,C567141,,,,
mondo:0014443,Bardet-Biedl syndrome 15,"['Bardet-Biedl syndrome type 15', 'WDPCP Bardet-Biedl syndrome', 'BBS15', 'Bardet-Biedl syndrome 15', 'Bardet-Biedl syndrome caused by mutation in WDPCP']",0110137,615992,,C3150127,,,,,,,,
mondo:0014444,Bardet-Biedl syndrome 16,"['Bardet-Biedl syndrome type 16', 'BBS16', 'Bardet-Biedl syndrome caused by mutation in SDCCAG8', 'Bardet-Biedl syndrome 16', 'SDCCAG8 Bardet-Biedl syndrome']",0110138,615993,,C3889474,,,,,,,,
mondo:0014445,Bardet-Biedl syndrome 17,"['BBS17', 'LZTFL1 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome 17', 'Bardet-Biedl syndrome caused by mutation in LZTFL1', 'Bardet-Biedl syndrome type 17']",0110139,615994,,C3714980,,,,,,,,
mondo:0014446,Bardet-Biedl syndrome 18,"['Bardet-Biedl syndrome type 18', 'BBIP1 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome caused by mutation in BBIP1', 'BBS18', 'Bardet-Biedl syndrome 18']",0110140,615995,,C3806174,,,,,,,,
mondo:0014447,Bardet-Biedl syndrome 19,"['Bardet-Biedl syndrome caused by mutation in IFT27', 'Bardet-Biedl syndrome 19', 'IFT27 Bardet-Biedl syndrome', 'Bardet-Biedl syndrome type 19', 'BBS19']",0110141,615996,,C3889475,,,,,,,,
mondo:0014448,"hyperthyroxinemia, familial dysalbuminemic","['hyperthyroxinemia, familial Dysalbuminemic', 'familial Dysalbuminemic hyperthyroxinemia', 'bisalbuminemia', 'FDAH', 'dysalbuminemic hyperthyroxinemia', 'hyperthyroxinemia, familial dysalbuminemic', 'familial Dysalbuminemic hyperthyroidism', 'dysalbuminemic hypertriiodothyroninemia', 'euthyroid hyperthyroxinemia 1', 'FDH']",,615999,276271,,,C131813,,D050010,,,,
mondo:0014449,congenital analbuminemia,"['analbuminemia', 'ANALBA']",,616000,86816,C4305253,"['-0.559', '-0.905', '-0.7744', '-0.4607', '0.178', '-0.4373', '-0.1119', '1.18', '-0.3367', '-0.09955', '-0.841', '0.0084', '-0.3464', '0.1531', '-0.1487', '-0.0208', '0.2058', '0.292', '-0.1593', '-0.4382', '0.479', '-0.772', '0.632', '-0.2566', '0.384', '0.05182', '0.06198', '0.01967', '-0.166', '-0.3906', '0.898', '-0.12103', '0.2656', '0.385', '-0.4634', '-0.3704', '0.04074', '-0.1255', '0.4946', '0.1914', '-0.2737', '0.2627', '0.4463', '-0.718', '0.0582', '-0.1583', '-0.1945', '-0.8', '-0.2273', '-0.1761', '0.5166', '0.04846', '0.07495', '-0.1697', '-0.262', '0.2004', '0.745', '-0.6533', '-0.3872', '0.03986', '-0.395', '0.5996', '0.505', '-0.2664', '-0.1898', '-0.0391', '0.1046', '0.4226', '-0.9517', '0.473', '-0.3997', '0.5693', '-0.3032', '0.6206', '0.532', '0.6265', '0.837', '0.5425', '-0.0665', '-0.4346', '-0.488', '0.353', '0.1388', '0.0931', '-0.1338', '0.3357', '0.456', '0.2386', '0.2312', '0.154', '0.1035', '-0.1764', '-0.558', '-0.2864', '0.45', '0.2156', '0.2913', '-0.6387', '0.2942', '-0.1526']",C124851,,,,,,
mondo:0014450,"breasts and/or nipples, aplasia or hypoplasia of, 2","['breasts and/or nipples, aplasia or hypoplasia of, 2', 'breasts and/or nipples, aplasia or hypoplasia of, type 2', 'isolated congenital breast hypoplasia/aplasia caused by mutation in PTPRF', 'BNAH2', 'PTPRF isolated congenital breast hypoplasia/aplasia']",,616001,,C4014918,"['-0.082', '0.0961', '0.06256', '-0.089', '0.08014', '-0.09296', '0.04578', '0.1204', '-0.1487', '-0.0892', '-0.0923', '0.005333', '-0.057', '-0.0081', '-0.1207', '-0.04205', '0.03183', '-0.06866', '-0.01672', '-0.2026', '-0.04785', '-0.07635', '0.1377', '-0.085', '0.07715', '-0.01653', '-0.06134', '-0.003025', '0.08154', '-0.1344', '0.1439', '-0.014206', '0.101', '0.0766', '0.1001', '-0.084', '-0.03232', '-0.002306', '0.00911', '-0.1455', '0.0512', '-0.066', '0.004734', '-0.05286', '-0.0474', '-0.1193', '0.01545', '0.1302', '0.001151', '0.004147', '-0.06107', '-0.03464', '0.0298', '0.02359', '-0.1279', '-0.03023', '0.05017', '-0.08875', '-0.2006', '0.013695', '0.03192', '0.125', '-0.0925', '0.04782', '-0.01167', '-0.04855', '0.1458', '0.11414', '-0.1142', '0.1399', '-0.1011', '0.0313', '0.05856', '-0.1573', '0.05338', '0.01794', '0.03168', '-0.0768', '-0.12305', '-0.17', '-0.0459', '-0.01007', '0.0225', '0.02698', '-0.04733', '-0.01007', '-0.01526', '0.2184', '0.1626', '-0.05566', '-0.02647', '0.145', '0.02655', '0.00739', '0.2874', '-0.03577', '0.1427', '-0.192', '0.02052', '0.07355']",,,,,,,
mondo:0014451,focal segmental glomerulosclerosis 7,"['focal segmental glomerulosclerosis 7', 'FSGS7', 'PAX2 focal segmental glomerulosclerosis', 'focal segmental glomerulosclerosis caused by mutation in PAX2', 'glomerulosclerosis, focal segmental, 7', 'focal segmental glomerulosclerosis type 7']",0111132,616002,656,C4014925,"['0.619', '-0.3982', '-0.04462', '0.3381', '-0.4143', '-0.2327', '0.2274', '0.314', '-0.4246', '-0.607', '0.2698', '-0.1262', '-0.4045', '0.619', '-0.4229', '-0.006718', '-0.01487', '0.3833', '0.8726', '-0.4546', '0.8354', '-0.8804', '0.4812', '0.519', '-0.0965', '-0.1283', '-0.4312', '0.2993', '-0.0537', '-0.3828', '1.291', '-0.246', '1.097', '0.012764', '-0.396', '-0.3735', '-0.0907', '0.2795', '0.3435', '-0.2457', '-0.2666', '0.0725', '-0.1635', '-0.6987', '0.1642', '-0.1598', '-0.3613', '-0.245', '-0.002832', '-0.6646', '-0.146', '0.4062', '1.042', '-0.6484', '-0.3057', '-0.544', '0.2174', '-0.07886', '-1.14', '-0.3306', '-0.3643', '-0.2208', '0.09406', '-0.6763', '-0.04495', '-0.154', '0.7617', '-0.2373', '-0.849', '0.2101', '-0.5615', '0.1074', '0.645', '-0.06274', '0.4631', '0.2433', '0.3245', '0.831', '-0.2488', '0.5664', '-0.1692', '-0.2683', '0.2189', '-0.1055', '0.2471', '-0.11523', '0.3433', '-0.3872', '0.331', '0.3616', '0.78', '0.5723', '-0.9473', '-0.06207', '0.3308', '0.5796', '-0.0705', '-0.6807', '-0.15', '-0.3076']",,,,,,,
mondo:0014452,familial dysfibrinogenemia,"['familial dysfibrinogenemia', 'congenital dysfibrinogenemia', 'hypodysfibrinogenemia, congenital', 'dysfibrinogenemia', 'dysfibrinogenemia, familial', 'dysfibrinogenemia, congenital', 'hypodysfibrinogenemia']",,616004,98881,CN207171,"['-0.512', '-0.308', '-0.3496', '-0.1953', '-0.1304', '0.00307', '0.0721', '0.149', '-0.1114', '0.1022', '0.313', '-0.2296', '-0.09924', '-0.0778', '-0.0649', '-0.186', '-0.00604', '0.07574', '-0.0639', '-0.3691', '-0.2168', '0.284', '0.731', '-0.02324', '0.0399', '0.112', '0.1469', '-0.2134', '0.0492', '0.1113', '0.2224', '-0.076', '0.333', '0.375', '-0.325', '-0.1644', '-0.2551', '-0.337', '0.06183', '-0.3276', '0.2224', '0.1713', '0.02191', '-0.1594', '-0.10754', '-0.2192', '-0.2573', '0.2119', '0.2168', '-0.03506', '0.4792', '-0.2139', '0.3118', '-0.09644', '-0.3735', '0.2491', '0.2986', '-0.274', '-0.474', '0.2817', '0.07684', '0.0756', '0.4304', '-0.2866', '0.1606', '0.1163', '0.1593', '0.1482', '-0.5894', '0.297', '-0.3804', '-0.1947', '-0.1893', '-0.1705', '0.5166', '0.3635', '0.565', '0.2825', '0.1921', '-0.2002', '-0.1936', '-0.1277', '0.01978', '0.04822', '0.0447', '0.1447', '0.0678', '0.1678', '0.12463', '-0.3604', '0.0704', '0.326', '-0.01839', '-0.0913', '0.605', '0.5146', '0.5645', '-0.71', '-0.2003', '0.2056']",C131659,,,286.3,,,
mondo:0014453,immunodeficiency 36,"['immunodeficiency 36', 'immunodeficiency type 36', 'IMD36']",0111949,616005,,C4014934,,,,,,,,
mondo:0014454,Hennekam lymphangiectasia-lymphedema syndrome 2,"['FAT4 Hennekam syndrome', 'Hennekam lymphangiectasia-lymphedema syndrome type 2', 'Hennekam lymphangiectasia-lymphedema syndrome 2', 'Hennekam syndrome caused by mutation in FAT4', 'HKLLS2']",,616006,,C4014939,,,,,,,,
mondo:0014455,cataract-growth hormone deficiency-sensory neuropathy-sensorineural hearing loss-skeletal dysplasia syndrome,"['cataracts, growth hormone deficiency, sensory neuropathy, sensorineural hearing loss, and skeletal dysplasia', 'CAGSSS']",,616007,436174,C4014942,"['-0.05093', '0.0925', '0.05975', '-0.03397', '0.09106', '-0.084', '0.0384', '0.11316', '-0.06256', '-0.07074', '-0.034', '-0.03198', '0.010544', '0.03912', '-0.0313', '-0.0648', '0.01901', '-0.00755', '-0.07043', '-0.1677', '0.010895', '-0.04886', '0.05667', '-0.03546', '0.0354', '-0.01933', '-0.03348', '-0.05496', '0.0408', '-0.05908', '0.0688', '-0.009544', '0.0889', '0.01028', '0.00217', '-0.04507', '0.01078', '-0.04987', '-0.007656', '-0.0708', '0.03464', '-0.04938', '0.038', '-0.05014', '0.01962', '-0.0973', '-0.03464', '0.05832', '0.0356', '0.0317', '-0.01362', '0.00453', '0.04602', '0.0373', '-0.0643', '-0.03983', '0.05432', '-0.0778', '-0.08105', '0.001634', '0.04517', '0.021', '-0.0314', '-0.001997', '-0.0447', '-0.003796', '0.10266', '0.1041', '-0.099', '0.07513', '-0.09906', '-0.0057', '0.0305', '-0.0773', '0.0206', '0.03085', '0.01825', '-0.002546', '-0.06384', '-0.0412', '-0.006073', '0.03363', '-0.05185', '0.07776', '-0.05197', '0.003511', '0.0561', '0.09485', '0.1229', '0.0716', '0.02501', '0.0693', '0.011635', '0.03032', '0.219', '0.02187', '0.08014', '-0.11066', '0.003056', '0.0793']",,,,,,,
mondo:0014456,autosomal recessive severe congenital neutropenia due to JAGN1 deficiency,"['neutropenia, severe congenital, 6, autosomal recessive', 'SCN6']",0112134,616022,423384,C4014954,,,,,,,,
mondo:0014457,hyperphosphatasia with intellectual disability syndrome 5,"['GPIBD11', 'hyperphosphatasia with intellectual disability syndrome 5', 'HPMRS5', 'PIGW hyperphosphatasia-intellectual disability syndrome', 'hyperphosphatasia with mental retardation syndrome 5', 'glycosylphosphatidylinositol biosynthesis defect 11', 'hyperphosphatasia with intellectual disability syndrome type 5', 'hyperphosphatasia with mental retardation syndrome type 5', 'hyperphosphatasia-intellectual disability syndrome caused by mutation in PIGW']",,616025,,C4014958,,,,,,,,
mondo:0014458,Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young,"['FRTS4 with MODY', 'Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young', 'Fanconi syndrome caused by mutation in HNF4A', 'HNF4A Fanconi syndrome', 'fanconi renotubular syndrome 4, with maturity-onset diabetes of the young', 'FRTS4']",0080760,616026,,C4014962,,,,,,,,
mondo:0014459,Adams-Oliver syndrome 5,"['Adams-Oliver syndrome 5', 'Adams-Oliver syndrome caused by mutation in Notch1', 'AOS5', 'NOTCH1 Adams-Oliver syndrome', 'Adams-Oliver syndrome type 5', 'Notch1 Adams-Oliver syndrome']",,616028,,C4014970,,,,,,,,
mondo:0014460,nail and teeth abnormalities-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome,"['short stature-nail dysplasia-marginal palmoplantar keratoderma-oral hyperpigmentation syndrome', 'ECTDS', 'ectodermal dysplasia/short stature syndrome', 'ectodermal dysplasia-short stature syndrome']",,616029,423454,C4014987,,,,,,,,
mondo:0014461,hypogonadotropic hypogonadism 22 with or without anosmia,"['HH22', 'FEZF1 hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism caused by mutation in FEZF1', 'hypogonadotropic hypogonadism 22, with or without anosmia', 'hypogonadotropic hypogonadism 22 with or without anosmia']",0090081,616030,,C4014988,,,,,,E23.0,,
mondo:0014462,focal segmental glomerulosclerosis 8,"['ANLN focal segmental glomerulosclerosis', 'glomerulosclerosis, focal segmental, 8', 'focal segmental glomerulosclerosis 8', 'FSGS8', 'focal segmental glomerulosclerosis type 8', 'focal segmental glomerulosclerosis caused by mutation in ANLN']",0111133,616032,,C4014993,,,,,,,,
mondo:0014464,progressive encephalopathy with leukodystrophy due to DECR deficiency,"['DECRD', 'dienoyl-CoA reductase deficiency', '2,4-dienoyl-CoA reductase deficiency', '2,4-alpha dienoyl-CoA reductase deficiency', 'DECR deficiency with hyperlysinemia']",,616034,431361,C1857252,"['-0.0991', '0.1006', '0.01744', '0.00237', '0.02943', '-0.1224', '0.013', '0.12274', '-0.10693', '-0.01312', '-0.05072', '-0.02296', '-0.0199', '-0.02255', '0.01221', '-0.09564', '-0.001767', '-0.04645', '-0.1057', '-0.2617', '-0.02023', '-0.09094', '0.1004', '-0.0145', '0.01704', '-0.05884', '-0.0433', '-0.0361', '-0.03568', '-0.04037', '0.0484', '0.0285', '0.1481', '0.0635', '-0.011116', '-0.06204', '-0.02219', '-0.068', '-0.03424', '-0.1079', '0.0692', '-0.1549', '0.0447', '-0.009056', '-0.0413', '-0.0866', '-0.033', '0.04453', '0.002539', '0.06122', '-0.009346', '0.02487', '0.02606', '-0.04395', '-0.03632', '-0.0438', '0.10675', '-0.0642', '-0.1351', '0.0659', '0.05582', '0.04633', '0.0971', '-0.01715', '0.0003371', '-0.00924', '0.1254', '0.1512', '-0.1389', '0.1448', '-0.1213', '0.01791', '0.03117', '-0.1181', '0.03836', '0.08295', '0.0685', '0.010284', '-0.0599', '-0.02348', '-0.00908', '-0.01007', '-0.08295', '0.084', '0.05225', '0.03186', '0.06073', '0.0793', '0.172', '0.01807', '0.07056', '0.1198', '-0.02269', '0.01883', '0.2173', '0.12427', '0.1178', '-0.1346', '0.02576', '0.07294']",,,C565624,,,,
mondo:0014465,primary ciliary dyskinesia 30,"['ciliary dyskinesia, primary, 30, with or without situs inversus', 'primary ciliary dyskinesia caused by mutation in CCDC151', 'primary ciliary dyskinesia 30 without situs inversus', 'ciliary dyskinesia, primary, type 30', 'primary ciliary dyskinesia type 30', 'CILD30', 'CCDC151 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 30']",0110624,616037,,C4015016,,,,,,,,
mondo:0014466,Neu-Laxova syndrome 2,"['PSAT1 Neu-Laxova syndrome', 'phosphoserine aminotransferase deficiency, prenatal form', 'Neu-Laxova syndrome 2', 'NEU-Laxova syndrome 2', 'NLS2', 'Neu-Laxova syndrome due to phosphoserine aminotransferase deficiency', 'Neu-Laxova syndrome caused by mutation in PSAT1', 'Neu-Laxova syndrome type 2']",0080075,616038,583602,C4015019,,,,,,,,
mondo:0014467,Charcot-Marie-Tooth disease recessive intermediate D,"['CMTRID', 'RI-CMT type D', 'Charcot-Marie-Tooth disease caused by mutation in COX6A1', 'Charcot-Marie-Tooth disease recessive intermediate type D', 'Charcot-Marie-Tooth disease, recessive intermediate D', 'autosomal recessive intermediate Charcot-Marie-Tooth disease type D', 'Charcot-Marie-Tooth disease, recessive Intermediate type D', 'COX6A1 Charcot-Marie-Tooth disease']",0110203,616039,435998,C4015029,,,,,,,,
mondo:0014468,congenital myasthenic syndrome 7,"['myasthenic syndrome, congenital, 7A, presynaptic, and distal motor neuropathy, autosomal dominant', 'myasthenic syndrome, presynaptic, congenital, with or without motor neuropathy', 'congenital myasthenic syndrome 7 presynaptic', 'SYT2 congenital myasthenic syndrome', 'congenital myasthenic syndrome type 7', 'CMS7', 'myasthenic syndrome, congenital, 7, presynaptic', 'congenital myasthenic syndrome caused by mutation in SYT2']",0110659,616040,,C4015038,,,,,,,,
mondo:0014469,autosomal recessive nonsyndromic hearing loss 103,"['deafness, autosomal recessive 103', 'autosomal recessive nonsyndromic deafness 103', 'autosomal recessive deafness 103', 'autosomal recessive nonsyndromic deafness caused by mutation in CLIC5', 'DFNB103', 'CLIC5 autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive type 103', 'autosomal recessive nonsyndromic deafness type 103']",0110464,616042,,C4015050,,,,,,,,
mondo:0014470,autosomal dominant nonsyndromic hearing loss 65,"['deafness, autosomal dominant type 65', 'autosomal dominant nonsyndromic deafness caused by mutation in TBC1D24', 'TBC1D24 autosomal dominant nonsyndromic deafness', 'deafness, autosomal dominant 65', 'autosomal dominant deafness 65', 'autosomal dominant nonsyndromic deafness type 65', 'autosomal dominant nonsyndromic deafness 65', 'DFNA65']",0110586,616044,,C3892048,,,,,,,,
mondo:0014471,mitochondrial proton-transporting ATP synthase complex deficiency,"['isolated ATP synthase deficiency', 'mitochondrial complex V (ATP synthase) deficiency', 'isolated mitochondrial respiratory chain complex V deficiency']",0111143,,254913,C4015062,"['-0.489', '0.3376', '0.1957', '0.0179', '-0.05704', '-0.4192', '0.2089', '0.3206', '-0.2437', '0.3218', '-0.2091', '-0.4338', '0.2313', '-0.2401', '0.0444', '0.03763', '0.03488', '-0.4797', '-0.2327', '-0.869', '0.1808', '-0.1298', '0.4211', '-0.0662', '-0.0927', '0.03687', '0.0911', '-0.0323', '0.01512', '-0.3943', '0.3313', '0.5864', '0.4875', '0.444', '-0.1588', '-0.4397', '-0.2004', '0.04398', '-0.3464', '-0.1248', '-0.06976', '-0.3447', '0.13', '0.303', '-0.1039', '-0.447', '0.2477', '0.2229', '-0.01906', '0.0173', '-0.5337', '0.1399', '-0.06158', '-0.07605', '0.06107', '-0.1826', '0.2096', '-0.1039', '-0.06464', '0.4905', '0.1123', '-0.09015', '0.545', '-0.010445', '-0.5166', '0.1086', '0.2502', '0.649', '-0.3386', '0.2463', '-0.4263', '0.3015', '0.0853', '0.06824', '0.2115', '0.1365', '0.1257', '-0.2927', '-0.1274', '0.11444', '0.2861', '-0.1047', '-0.3518', '0.1873', '0.4185', '0.01714', '0.1333', '0.2104', '0.4158', '-0.0535', '0.5903', '-0.008224', '0.09424', '0.05573', '0.4841', '0.4653', '0.2842', '0.02623', '-0.05136', '0.0893']",,,,,,,
mondo:0014472,periodic fever-infantile enterocolitis-autoinflammatory syndrome,"['AUTOINFLAMMATION with infantile enterocolitis', 'NLRC4-related infantile enterocolitis-autoinflammatory syndrome', 'NLRC4-related MAS', 'NLRC4-related autoinflammatory syndrome with MAS', 'autoinflammation with infantile enterocolitis', 'NLRC4-related autoinflammatory syndrome with macrophage activation syndrome', 'NLRC4-related macrophage activation syndrome', 'AIFEC']",,616050,436166,C4015067,,,,,,,,
mondo:0014473,"microcephaly 13, primary, autosomal recessive","['CENPE autosomal recessive primary microcephaly', 'autosomal recessive primary microcephaly caused by mutation in CENPE', 'MCPH13', 'microcephaly 13, primary, autosomal recessive']",0070283,616051,,C4015080,,,,,,,,
mondo:0014474,autosomal recessive limb-girdle muscular dystrophy type 2U,"['MDDGC7', 'muscular dystrophy limb-girdle type 2U', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in ISPD', 'LGMD2U', 'autosomal recessive limb-girdle muscular dystrophy due to ISPD deficiency', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 7', 'muscular dystrophy, limb-girdle, type 2U', 'ISPD autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy-dystroglycanopathy (limb-girdle) type C7']",0110295,616052,352479,C4015095,"['-0.1702', '-0.448', '-0.693', '-0.2255', '0.54', '-1.131', '0.188', '0.681', '-1.871', '-0.7334', '0.1283', '0.5044', '-0.1855', '0.6978', '0.1543', '0.1385', '-0.8105', '-0.4836', '-0.581', '-0.8228', '0.204', '0.1782', '0.2219', '0.4688', '0.239', '0.1565', '-0.2174', '-0.928', '0.1932', '-0.3315', '0.6934', '-0.183', '0.5137', '0.3015', '-0.0727', '0.08203', '-0.5713', '0.16', '0.05746', '-0.5576', '0.1659', '-0.2825', '-0.6235', '0.4307', '-0.134', '0.3599', '0.08356', '0.862', '-0.12164', '0.507', '0.3027', '-0.0909', '0.2805', '-0.808', '0.0863', '-0.6743', '0.326', '0.849', '-0.12036', '0.08154', '0.03134', '0.2289', '0.02135', '-0.1212', '-0.005608', '0.1191', '0.01018', '0.7036', '-0.3516', '-0.3079', '-0.1615', '0.485', '0.0984', '-0.1545', '0.6123', '0.5537', '0.3022', '0.5684', '-0.02286', '0.0721', '0.01377', '-0.0713', '0.1904', '0.01784', '0.01892', '0.193', '-0.0669', '-0.3357', '0.8726', '0.11224', '-0.1917', '-0.007275', '0.1438', '0.8867', '-0.06866', '0.2458', '0.251', '-0.4006', '-0.0998', '0.04132']",,,,,,,
mondo:0014475,spinocerebellar ataxia type 40,"['SCA40', 'spinocerebellar ataxia type 40', 'spinocerebellar ataxia 40']",0050986,616053,423275,CN237494,"['-0.1849', '-0.3452', '0.00804', '0.2294', '-0.3345', '-0.9404', '0.1602', '-0.006683', '-0.652', '-0.914', '0.2913', '0.2651', '-0.2223', '0.3237', '0.449', '-0.2778', '-0.10114', '-0.307', '0.06995', '-0.993', '-0.0769', '-0.3232', '0.1351', '-0.685', '0.5186', '-0.5737', '-0.3154', '0.1873', '-0.1969', '-1.069', '0.1709', '0.5737', '-0.5005', '-0.1621', '0.254', '0.09534', '-0.2084', '0.1854', '0.6084', '0.4253', '0.3906', '0.2251', '-0.502', '0.4954', '0.651', '-0.6377', '0.10284', '0.4504', '0.3481', '-0.1888', '-0.1467', '0.3203', '-0.1189', '-0.438', '0.096', '-0.7793', '0.3867', '0.4006', '-0.07245', '0.4978', '-0.4207', '0.2678', '0.2979', '-0.3232', '-0.467', '0.5312', '0.234', '0.666', '-0.5444', '0.4766', '0.796', '0.3599', '-0.1696', '-0.6406', '0.779', '0.4253', '0.178', '0.405', '0.0922', '0.4211', '-0.2407', '-0.8945', '0.4265', '0.72', '-0.3022', '-0.779', '0.1423', '0.05115', '0.676', '0.4934', '0.4814', '0.539', '0.1299', '0.12305', '1.085', '0.9224', '0.3694', '0.422', '-0.4636', '-0.0573']",,0009057,,,,,
mondo:0014476,episodic ataxia type 8,"['episodic ataxia type 8', 'episodic ataxia, type 8', 'EA8', 'episodic ataxia with slurred speech']",0050996,616055,401953,C4015108,,,,,,,,
mondo:0014477,"developmental and epileptic encephalopathy, 26","['EIEE26', 'developmental and epileptic encephalopathy 26', 'DEE26', 'epileptic encephalopathy, early infantile, type 26', 'epileptic encephalopathy, early infantile, 26', 'early infantile epileptic encephalopathy 26', 'KCNB1 early infantile epileptic encephalopathy', 'early infantile epileptic encephalopathy caused by mutation in KCNB1']",0080461,616056,,C4015119,,,,,,,,
mondo:0014478,mirror movements 3,"['MRMV3', 'familial congenital mirror movements caused by mutation in DNAL4', 'mirror movements 3', 'DNAL4 familial congenital mirror movements', 'mirror movements type 3']",,616059,,C4015124,,,,,,,,
mondo:0014479,"porokeratosis 8, disseminated superficial actinic type","['porokeratosis 8, disseminated superficial actinic type', 'POROK8']",,616063,,C4015128,,,,,,,,
mondo:0014480,"46,XY sex reversal 9","['SRXY9', '46,XY SEX reversal 9', '46XY sex reversal 9', '46,XY Sex reversal, Zfpm2-related', '46,XY sex reversal 9', '46,XY Sex reversal type 9']",0111770,616067,,C4015129,,,,,,,,
mondo:0014481,"inflammatory skin and bowel disease, neonatal, 2","['EGFR neonatal inflammatory skin and bowel disease', 'inflammatory skin and bowel disease, neonatal, type 2', 'inflammatory skin and bowel disease, neonatal, 2', 'NISBD2', 'neonatal inflammatory skin and bowel disease caused by mutation in EGFR']",,616069,,C4015130,,,,,,,,
mondo:0014482,"intellectual disability, autosomal dominant 29","['SETBP1 related developmental delay', 'autosomal dominant intellectual disability 29', 'SETBP1 intellectual disability-expressive aphasia-facial dysmorphism syndrome', 'SETBP1 disorder', 'mental retardation, autosomal dominant 29', 'intellectual disability, autosomal dominant type 29', 'intellectual disability, autosomal dominant 29', 'SETBP1-related disorder', 'intellectual disability-expressive aphasia-facial dysmorphism syndrome caused by mutation in SETBP1', 'mental retardation, autosomal dominant type 29', 'autosomal dominant mental retardation 29', 'MRD29', 'autosomal dominant non-syndromic intellectual disability 29', 'SETBP1-related intellectual disability']",0070059,616078,,C4015141,,,,,,,,
mondo:0014483,retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies,"['retinal dystrophy with inner retinal dysfunction and ganglion cell abnormalities', 'RDGCA', 'retinal dystrophy with inner nuclear layer and ganglion cell anomalies']",,616079,397758,C4015146,"['-0.7188', '-0.0631', '0.4607', '-0.0677', '0.3647', '-0.2104', '-0.1265', '0.2327', '-0.1534', '-0.3994', '-0.05368', '-0.373', '-0.353', '-0.2952', '-0.129', '-0.554', '0.01707', '0.02034', '-0.1766', '-0.4678', '0.011826', '-0.332', '-0.1628', '0.7256', '0.1377', '0.02011', '-0.2028', '-0.1593', '-0.2888', '0.1451', '0.3445', '0.4075', '0.2457', '-0.05814', '-5.28e-05', '-0.002876', '0.1382', '-0.0823', '0.03256', '-0.674', '-0.1752', '-0.07983', '0.1744', '0.1599', '-0.257', '-0.2666', '-0.02182', '-0.2556', '0.2896', '-0.076', '0.29', '0.2477', '0.1002', '-0.34', '0.1454', '-0.239', '0.8164', '0.1471', '-0.6367', '-0.0075', '0.04785', '-0.0345', '0.1227', '0.3918', '0.00698', '0.147', '0.369', '0.621', '-0.1996', '0.551', '-0.4038', '-0.1752', '0.03543', '0.09143', '0.2776', '-0.3367', '0.324', '0.4607', '-0.0749', '-0.2196', '0.3223', '-0.1952', '-0.01646', '0.51', '-0.578', '-0.4722', '0.1692', '0.59', '0.2793', '0.09125', '0.01953', '0.3542', '0.1818', '-0.0389', '0.786', '-0.02505', '0.3677', '-0.334', '-0.05145', '0.5054']",,,,,H35.5,,
mondo:0014484,"microcephaly 12, primary, autosomal recessive","['CDK6 autosomal recessive primary microcephaly', 'microcephaly 12, primary, autosomal recessive', 'MCPH12', 'autosomal recessive primary microcephaly caused by mutation in CDK6']",0070284,616080,,C4015156,,,,,,,,
mondo:0014485,"pontocerebellar hypoplasia, type 1C","['PCH1C', 'EXOSC8 pontocerebellar hypoplasia type 1', 'hypomyelination with spinal muscular atrophy and cerebellar hypoplasia', 'pontocerebellar hypoplasia type 1 caused by mutation in EXOSC8', 'pontocerebellar hypoplasia, type 1C']",0112334,616081,,C4015160,,,,,,,,
mondo:0014486,"intellectual disability, autosomal dominant 30","['MRD30', 'autosomal dominant non-syndromic intellectual disability 30', 'ZMYND11 intellectual disability-expressive aphasia-facial dysmorphism syndrome', 'intellectual disability, autosomal dominant type 30', 'mental retardation, autosomal dominant 30', 'mental retardation, autosomal dominant type 30', 'intellectual disability, autosomal dominant 30', 'autosomal dominant intellectual disability 30', 'autosomal dominant mental retardation 30', 'intellectual disability-expressive aphasia-facial dysmorphism syndrome caused by mutation in ZMYND11']",0070060,616083,,C4015167,,,,,,,,
mondo:0001341,selective IgA deficiency disease,"['IgA deficiencies', 'IgA deficiency', 'selective immunoglobulin A deficiency', 'deficiencies, IgA', 'gamma-A-globulin deficiency', 'immunoglobulin A deficiency', 'deficiency, IgA', 'immunoglobulin alpha deficiency', 'SIgAD', 'selective IgA immunodeficiency']",11701,,69127,C4049006,,C26964,1001929,D017098,,,,
mondo:0001342,dysgammaglobulinemia,"['dysgammaglobulinemia (finding)', 'dysgammaglobulinemia (disease)', 'dysgammaglobulinemia']",11702,,,C0013374,,,,D004406,,,,0002961
mondo:0001343,impaired renal function disease,['disease of kidney'],11705,,,,,,,,588.9,N25,,
mondo:0001345,antidepressant type abuse,,11718,,,,,,,,305.8,,,
mondo:0001347,facioscapulohumeral muscular dystrophy,"['muscular dystrophy, Landouzy-Dejerine', 'Landouzy-Dejerine myopathy', 'FSH dystrophy', 'facioscapulohumeral muscular dystrophy', 'facioscapulohumeral myopathy', 'FSHD', 'facioscapulohumeral dystrophy', 'Landouzy Dejerine muscular dystrophy', 'Landouzy-Dejerine muscular dystrophy']",11727,,269,,"['0.2009', '-0.6016', '-0.613', '-0.0263', '0.3018', '-0.881', '0.2937', '0.7534', '-1.593', '-0.709', '0.0561', '0.572', '-0.11847', '0.8994', '0.2344', '0.3823', '-0.7646', '-0.6406', '-0.2139', '-0.8022', '0.06714', '-0.0427', '0.336', '0.2306', '0.301', '-0.1069', '0.0968', '-0.889', '0.3838', '-0.1346', '0.84', '0.07196', '0.2292', '0.1138', '0.2764', '-0.1665', '-0.3325', '0.3386', '-0.0981', '-0.242', '-0.01756', '-0.2737', '-0.1555', '0.3735', '-0.12256', '0.2496', '-0.2815', '0.3855', '-0.08417', '0.3308', '0.2708', '-0.1532', '0.2422', '-0.5024', '0.19', '-0.575', '0.6377', '0.6904', '-0.06134', '-0.2284', '0.3464', '-0.063', '-0.07825', '-0.094', '0.273', '0.258', '-0.0415', '0.5166', '-0.3022', '-0.3113', '-0.3862', '0.129', '0.02753', '-0.1664', '0.6387', '0.5845', '-0.0631', '0.2686', '0.1709', '-0.01994', '0.3022', '-0.2507', '-0.188', '0.2164', '0.1752', '0.2559', '-0.274', '-0.2957', '0.4683', '0.006207', '-0.3745', '-0.1819', '0.309', '1.084', '0.1304', '-0.02008', '0.2231', '-0.4714', '0.1315', '0.06476']",C84704,,D020391,,,10064087,
mondo:0001349,odontoclasia,,11736,,,C0341004,,,,,521.05,,,
mondo:0001350,parametrium malignant neoplasm,"['parametrium cancer', 'malignant parametrium neoplasm', 'malignant neoplasm of parametrium', 'cancer of parametrium']",11746,,,C0153581,,,,,183.4,,,
mondo:0001351,uterine adnexa cancer,,11747,,,,,,,,183.9,,,
mondo:0001352,round ligament malignant neoplasm,"['malignant neoplasm of round ligament', 'round ligament of uterus cancer', 'malignant round ligament of uterus neoplasm', 'malignant neoplasm of round ligament of uterus', 'cancer of round ligament of uterus']",11748,,,C0346867,,,,,183.5,,,
mondo:0001353,Bordetella parapertussis infectious disease,"['Bordetella parapertussis caused disease or disorder', 'Bordetella parapertussis whooping cough']",11750,,,C0275742,,,,,033.1,A37.1,,
mondo:0001355,ocular siderosis,"['siderosis of globe', 'camera-type eye hemosiderosis', 'hemosiderosis of camera-type eye', 'siderosis of eye', 'siderosis bulbi']",11754,,,C0271001,,,,,360.23,,,
mondo:0001356,iron deficiency anemia,"['iron-deficiency anemia', 'iron-deficiency anaemia']",11758,,,C0162316,,C84484,,D018798,280.9,,,
mondo:0001357,hypochromic anemia,"['hypochromic anemia', 'anemia hypochromic', 'anaemia hypochromic', 'hypochromic anemia (disease)', 'hypochromic anaemia (disease)']",11759,,,C0002884,,C34380,,,,,,0001931
mondo:0001358,bronchial disorder,"['bronchospasm', 'bronchus disease', 'disease of bronchus', 'disorder of bronchus', 'bronchus disease or disorder']",1176,,,C0006261,,C34439,1002018,D001982,519.19,,,
mondo:0001360,blind hypotensive eye,,11766,,,C0154788,,,,,360.41,,,
mondo:0001361,spontaneous ocular nystagmus,"['searching eye movements', 'ocular nystagmus', 'visual deprivation nystagmus']",11771,,,C0271384,,,,,379.53,H55.03,,
mondo:0001363,blind hypertensive eye,,11776,,,C0154789,,,,,360.42,,,
mondo:0001364,regular astigmatism,,11781,,,C0152193,,,,,367.21,,,
mondo:0001365,necrosis of ear ossicle,['partial loss or necrosis of ear ossicles'],11783,,,,,,,,385.24,,,
mondo:0001366,splenic sequestration,,11786,,,,,,,,289.52,,,
mondo:0001367,chronic congestive splenomegaly,"['congestive splenomegaly, chronic']",11787,,,C0398661,,,,,289.51,D73.2,,
mondo:0001368,phthisical cornea,,11793,,,C0155102,,,,,371.05,,,
mondo:0001369,chronic laryngitis,"['laryngitis, chronic']",11797,,,C0155836,,C26975,,,476.0,J37.0,,
mondo:0001370,pericardial effusion,"['fluid, pericardial', 'pericardial effusion (disease)', 'pericardial fluid', 'pericardial effusion']",118,,,C0031039,,C3319,,D010490,,,,0001698
mondo:0001371,protein-energy malnutrition,['Protein energy malnutrition'],11801,,,,,C34952,,D011502,269.8,,,
mondo:0001372,bladder neck cancer,"['cancer of neck of urinary bladder', 'malignant tumour of bladder neck', 'malignant neck of urinary bladder neoplasm', 'malignant neoplasm of neck of urinary bladder', 'malignant neoplasm of urinary bladder neck', 'malignant tumor of bladder neck', 'neck of urinary bladder cancer']",11809,,,,,,,,188.5,,,
mondo:0001373,urinary bladder posterior wall cancer,['malignant neoplasm of posterior wall of urinary bladder'],11811,,,C0153612,,,,,188.4,,,
mondo:0001374,bladder sarcoma,"['bladder sarcoma', 'sarcoma of urinary bladder', 'sarcoma of bladder', 'sarcoma of the bladder', 'urinary bladder sarcoma', 'sarcoma of the urinary bladder']",11812,,,C0349666,,C4669,,,,,,
mondo:0001375,bladder trigone cancer,"['cancer of trigone of urinary bladder', 'malignant trigone of urinary bladder neoplasm', 'trigone of urinary bladder cancer', 'malignant neoplasm of trigone of urinary bladder']",11813,,,C0496826,,,,,188.0,,,
mondo:0001376,urinary bladder anterior wall cancer,['malignant neoplasm of anterior wall of urinary bladder'],11814,,,C0153611,,,,,188.3,,,
mondo:0001377,vitreous syneresis,['vitreous degeneration'],11816,,,C0155366,,,,,379.21,,,
mondo:0001378,urachus cancer,"['urachus cancer', 'malignant tumour of urachus', 'malignant urachus neoplasm', 'cancer of urachus', 'malignant tumor of urachus', 'malignant neoplasm of urachus']",11817,,,C0153615,,,,,188.7,,,
mondo:0001379,ureteric orifice cancer,"['ureteral orifice cancer', 'malignant tumor of ureteric orifice', 'malignant tumour of ureteric orifice', 'orifice of the ureter', 'malignant ureteral orifice neoplasm', 'cancer of ureteral orifice', 'malignant neoplasm of ureteral orifice', 'malignant neoplasm of ureteric orifice of urinary bladder']",11818,,,C0153614,,,,,188.6,,,
mondo:0001380,bladder dome cancer,"['malignant neoplasm of apex of urinary bladder', 'superior surface of bladder', 'malignant neoplasm of fundus of urinary bladder', 'malignant tumor of vault of bladder', 'malignant neoplasm of dome of urinary bladder', 'fundus of urinary bladder cancer', 'malignant tumour of vault of bladder', 'malignant fundus of urinary bladder neoplasm', 'cancer of fundus of urinary bladder']",11820,,,C0496827,,,,,188.1,,,
mondo:0001381,bladder lymphoma,"['lymphoma of bladder', 'lymphoma of urinary bladder', 'lymphoma of the urinary bladder', 'urinary bladder lymphoma', 'primary bladder lymphoma', 'lymphoma of the bladder']",11821,,,C1332561,,C6164,,,,,,
mondo:0001382,hepatorenal syndrome,['hepato-renal syndrome'],11823,,,C0019212,,C113400,,D006530,572.4,K76.7,,
mondo:0001383,degenerative myopia,"['pathological myopia', 'degenerative progressive high myopia', 'progressive high (degenerative) myopia', 'progressive high myopia']",11829,,,C0154778,,,0004207,D047728,360.21,H44.2,,
mondo:0001384,myopia,"['short-sightedness', 'myopia (disease)', 'myopia', 'near vision', 'near-sightedness']",11830,,,C0027092,"['0.299', '-0.4404', '-0.208', '1.246', '0.4058', '-0.3057', '-0.307', '0.866', '-0.5903', '-0.3582', '0.4028', '0.0406', '0.2351', '0.7114', '-0.3562', '-0.3337', '-0.1963', '-0.014404', '-0.2566', '-0.3267', '-0.6436', '0.2028', '-0.4243', '0.306', '-0.034', '0.09015', '0.04254', '0.1823', '0.2144', '0.1395', '0.2263', '-0.207', '0.487', '0.355', '0.003668', '0.3555', '0.06384', '-0.571', '-0.0962', '-0.723', '0.8345', '0.0675', '-0.1621', '-0.5273', '0.1747', '0.0896', '0.003523', '-0.348', '0.1049', '0.5444', '0.05066', '0.05957', '-0.2363', '-0.621', '0.3276', '-0.1564', '0.3464', '0.8535', '-0.3408', '-0.3848', '0.321', '0.4062', '-0.5835', '0.518', '-0.232', '0.532', '0.6313', '0.436', '0.02364', '0.582', '0.4539', '0.5293', '-0.041', '-0.635', '0.3267', '0.08636', '-0.0939', '0.6685', '-0.253', '0.1117', '0.2406', '0.04138', '-0.322', '1.216', '0.5347', '-0.6187', '0.1918', '0.3022', '0.508', '0.561', '-0.014885', '0.571', '-0.649', '0.33', '0.556', '-0.2603', '-0.31', '-0.6187', '-0.7495', '-0.068']",,0003927,D009216,367.1,H52.1,,0000545
mondo:0001385,cortical blindness,,11831,,,C0155320,,C118707,,D019575,377.75,,,
mondo:0001386,visual epilepsy,"['epilepsy, visual']",11832,,,C0270824,,C3980,,D012640,,,,
mondo:0001387,penile sarcoma,"['sarcoma of the penis', 'penile sarcoma', 'sarcoma of penis', 'penis sarcoma']",11838,,,C0238352,,C7730,,,,,,
mondo:0001388,glans penis cancer,"['glans penis cancer', 'cancer of glans penis', 'malignant glans penis neoplasm', 'malignant tumor of glans penis', 'malignant neoplasm of glans penis', 'malignant tumour of glans penis']",11839,,,C0153599,,,,,187.2,,,
mondo:0001389,congenital coronary artery anomaly,"['coronary artery abnormality', 'coronary artery abnormality [ambiguous]', 'coronary artery anomaly, congenital', 'congenital anomaly of coronary artery', 'coronary artery anomaly']",11843,,,,,,,,746.85,,,
mondo:0001390,transient refractive change,,11850,,,C0155000,,,,,367.81,,,
mondo:0001391,indeterminate leprosy,"['uncharacteristic leprosy', 'indeterminate leprosy [group I]']",11851,,,C0021192,,,,,030.2,A30.0,,
mondo:0001392,monocular exotropia,,11853,,,C0152206,,,,,378.11,,,
mondo:0001393,peripheral focal chorioretinitis,,11864,,,C0339394,,,,,363.04,,,
mondo:0001394,chronic erythremia,,11868,,,,,,,,207.1,,,
mondo:0001395,macular keratitis,,11871,,,C0155076,,,,,370.22,,,
mondo:0001396,abnormal threshold of rods,['abnormal dark adaptation curve'],11874,,,C0155019,,,,,368.63,H53.61,,
mondo:0001397,mononeuropathy,,1188,,,C0494491,,,,D020422,,,,
mondo:0001398,ureter benign neoplasm,"['benign ureter tumor', 'benign ureteral tumour', 'benign neoplasm of ureter', 'benign tumour of the ureter', 'benign ureter neoplasm', 'benign tumor of the ureter', 'benign ureter tumour', 'benign ureteral neoplasm', 'ureter benign neoplasm', 'ureteral benign neoplasm', 'benign tumor of ureter', 'benign ureteric neoplasm', 'benign neoplasm of the ureter', 'ureteral tumour', 'ureteral tumor', 'benign tumour of ureter', 'benign ureteral tumor']",11885,,,,,C3617,,D014516,223.2,,,
mondo:0001399,ureter leiomyoma,"['ureteral leiomyoma', 'leiomyoma of the ureter', 'ureter leiomyoma', 'leiomyoma of ureter']",11887,,,C1336875,,C6161,,,,,,
mondo:0001400,schwannoma of ureter,"['ureter neurilemmoma', 'neurilemmoma of ureter', 'ureter schwannoma', 'ureteral neurilemmoma', 'ureteral schwannoma', 'neurilemmoma of the ureter', 'schwannoma of the ureter']",11888,,,C1336877,,C6162,,,,,,
mondo:0001401,female breast nipple and areola cancer,"['malignant neoplasm of nipple or areola of female breast', 'malignant neoplasm of nipple and areola of female breast']",11889,,,C0024621,,,,,174.0,,,
mondo:0001402,vaginal cancer,"['malignant neoplasm of the vagina', 'malignant neoplasm of vagina', 'malignant vagina tumour', 'malignant vaginal tumour', 'malignant tumor of the vagina', 'malignant vaginal tumor', 'vaginal tumour', 'vagina cancer', 'cancer of vagina', 'malignant tumour of the vagina', 'vagina neoplasm', 'malignant vagina tumor', 'malignant vagina neoplasm', 'malignant tumor of vagina', 'malignant tumour of vagina', 'vaginal tumor', 'malignant vaginal neoplasm']",119,,,,,C7410,,D014625,184.0,,,
mondo:0001403,labium majus cancer,"['malignant labium majora neoplasm', 'malignant tumour of labia majora', 'malignant labia majora tumour', 'malignant tumor of the labia majora', 'malignant neoplasm of labia majora', 'malignant tumor of labia majora', 'malignant labia majora neoplasm', 'malignant neoplasm of labium majora', 'malignant tumour of the labia majora', 'labium majora cancer', 'malignant neoplasm of the labia majora', 'malignant labia majora tumor', 'cancer of labium majora']",11905,,,C0496814,,C7638,,,184.1,,,
mondo:0001404,ecthyma,,11907,,,C0013568,,,1000689,D004473,686.8,,,
mondo:0001405,dermatophytosis of groin and perianal area,"['dermatophytosis of groin & perianal area', 'dermatophytosis of groin and perianal area', 'tinea cruris', 'Dhobie itch']",11917,,,C0011638,,C34535,,,110.3,,,
mondo:0001406,peripheral nervous system neoplasm,"['peripheral nervous system tumor', 'CNS-excluded nervous sys. cancer', 'tumour of the peripheral nervous system', 'nerve sheath neoplasm', 'neoplasm of the peripheral nerve', 'neoplasms, PNS', 'peripheral nerve tumor', 'tumour of peripheral nervous system', 'neoplasm of PNS', 'tumor of PNS', 'neoplasms, peripheral nervous system', 'peripheral nervous system neoplasm', 'tumour of the PNS', 'tumor of the peripheral nervous system', 'tumour of the peripheral nerve', 'tumor of peripheral nerve', 'PNS tumor', 'nerve sheath tumours', 'neoplasm of peripheral nerve', 'tumor of the peripheral nerve', 'tumour of PNS', 'neoplasm of peripheral nervous system', 'tumor of peripheral nervous system', 'PNS neoplasm', 'peripheral nerve neoplasm', 'nerve sheath tumors', 'neoplasm of the PNS', 'peripheral nervous system neoplasm (disease)', 'tumor of the PNS', 'PNS tumour', 'PNS neoplasms', 'peripheral nerve tumour', 'peripheral nervous system tumour', 'neoplasm of the peripheral nervous system', 'tumour of peripheral nerve']",1192,,,C0031118,,C3321,,D010524,239.2,,,
mondo:0001407,tracheal cancer,"['malignant tracheal tumour', 'malignant tumor of trachea', 'trachea cancer', 'malignant trachea tumour', 'malignant tumour of trachea', 'tracheal neoplasm', 'Ca trachea', 'malignant trachea neoplasm', 'malignant tumour of the trachea', 'malignant neoplasm of trachea', 'malignant tracheal neoplasm', 'malignant trachea tumor', 'malignant neoplasm of the trachea', 'malignant tracheal tumor', 'cancer of trachea', 'malignant tumor of the trachea']",11920,,,C0153489,,C9346,,,162.0,C33,,
mondo:0001408,ischemic neuropathy,"['ischemic peripheral neuropathy', 'ischaemic peripheral neuropathy']",1195,,,C0238309,,C27025,,,356.9,,,
mondo:0001409,esophagitis,"['oesophagus inflammation', 'esophagitis', 'inflammation of oesophagus', 'esophagitis (disease)', 'esophagus inflammation', 'acute esophagitis']",11963,,,C0149882,,C9224,,D004941,530.12,,,0100633
mondo:0001410,postmenopausal atrophic vaginitis,"['senile vaginitis', 'atrophic vaginitis']",11968,,,C0221392,,,1001271,D059268,627.3,N95.2,,
mondo:0001411,synostosis,,11971,,,,,,,D013580,,,,
mondo:0001412,conjunctival concretion,,11988,,,,,,,,372.54,,,
mondo:0001413,ulceroglandular tularemia,,11990,,,C0152941,,,,,021.0,A21.0,,
mondo:0001414,osteopoikilosis,"['spotted bones', 'osteopathia condensans disseminata', 'osteopoikilosis (disease)', 'osteopoikilosis']",11991,,,,,C84985,,D010023,756.53,,,0010739
mondo:0001415,atrophy of testis,['testicular atrophy'],11994,,,C0156312,,C123259,,,608.3,N50.0,,
mondo:0001416,female reproductive organ cancer,"['malignant neoplasm of the female reproductive system', 'malignant female reproductive system tumor', 'female reproductive organ cancer', 'gynecologic cancer', 'malignant tumor of the female reproductive system', 'malignant tumor of female reproductive system', 'malignant tumour of female reproductive system', 'malignant female reproductive system neoplasm', 'cancer of female reproductive organ', 'malignant female reproductive system tumour', 'malignant gynecologic tumour', 'malignant neoplasm of female reproductive organ', 'malignant neoplasm of female reproductive system', 'malignant gynecologic neoplasm', 'malignant tumour of the female reproductive system', 'female reproductive cancer', 'malignant gynecologic tumor', 'malignant female reproductive organ neoplasm', 'malignant neoplasm of female genital organ']",120,,,,,C4913,,,184,C51-C58,,
mondo:0001417,tracheal lymphoma,"['lymphoma of trachea', 'lymphoma of the trachea', 'tracheal lymphoma', 'primary tracheal lymphoma', 'trachea lymphoma']",12001,,,C1336773,,C6248,,,,,,
mondo:0001418,trachea sarcoma,"['sarcoma of the trachea', 'sarcoma of trachea', 'trachea sarcoma', 'tracheal sarcoma']",12002,,,C1336774,,C6050,,,,,,
mondo:0001419,trachea squamous cell carcinoma,"['epidermoid carcinoma of trachea', 'epidermoid carcinoma of the trachea', 'tracheal squamous cell carcinoma', 'tracheal epidermoid carcinoma', 'squamous cell carcinoma of trachea', 'squamous cell carcinoma of the trachea', 'trachea squamous cell carcinoma', 'trachea epidermoid carcinoma']",12003,,,C0345946,,C4448,1000600,,,,,
mondo:0001420,trigeminal nerve neoplasm,"['fifth cranial nerve neoplasm', 'trigeminal nerve tumour', 'tumour of the fifth cranial nerve', 'neoplasm of the fifth cranial nerve', 'tumor of fifth cranial nerve', 'cranial nerve V neoplasms', 'tumour of fifth cranial nerve', 'trigeminal nerve tumors', 'trigeminal nerve tumours', 'cranial nerve V tumours', 'neoplasm of the trigeminal nerve', 'fifth cranial nerve tumor', 'trigeminal nerve tumor', 'cranial nerve V tumors', 'neoplasm of fifth cranial nerve', 'fifth cranial nerve tumour', 'neoplasms, cranial nerve V', 'tumor of the fifth cranial nerve', 'trigeminal nerve neoplasm', 'tumour of trigeminal nerve', 'tumors, cranial nerve V', 'tumour of the trigeminal nerve', 'trigeminal nerve neoplasms', 'tumor of the trigeminal nerve', 'neoplasm of trigeminal nerve', 'trigeminal nerve neoplasm (disease)', 'tumor of trigeminal nerve']",1201,,,C1263897,,C5122,,,239.7,,,
mondo:0001421,frontal lobe neoplasm,"['tumor of the frontal lobe', 'frontal lobe neoplasm (disease)', 'neoplasm of frontal lobe', 'frontal lobe tumor', 'tumour of frontal lobe', 'frontal lobe tumour', 'neoplasm of the frontal lobe', 'malignant neoplasm of frontal lobe', 'tumour of the frontal lobe', 'tumor of frontal lobe']",12016,,,C1263886,,C5572,,,191.1,,,
mondo:0001422,primary aldosteronism,"['primary hyperaldosteronism', 'Conn^s syndrome', 'primary aldosteronism', 'Conn syndrome']",12028,,,,,C34510,,D006929,255.12,E26.0,,
mondo:0001423,drug-induced mental disorder,,1203,,,,,,,,292.89,,,
mondo:0001426,mediastinum neurofibroma,"['mediastinal neurofibroma', 'neurofibroma of mediastinum', 'neurofibroma of the mediastinum', 'mediastinum neurofibroma']",12064,,,C1334674,,C6631,,,,,,
mondo:0001427,Dieulafoy lesion,"['Dieulafoy lesion (hemorrhagic) of stomach and duodenum', 'Dieulafoy^s lesion', 'Dieulafoy lesion (hemorrhagic) of intestine', 'Exulceratio simplex Dieulafoy', 'Dieulafoy disease']",12070,,,C0341217,,,,,537.84,K31.82,,
mondo:0001428,pylorospasm,,12072,,,C0152163,,,,,537.81,,,
mondo:0001429,transient arthropathy,"['transient arthropathy involving multiple sites', 'transient arthropathy involving upper arm', 'transient arthropathy involving lower leg', 'transient arthropathy involving pelvic region and thigh', 'transient arthropathy involving hand', 'transient arthropathy involving shoulder region', 'transient arthropathy involving forearm']",12084,,,,,C35761,,,716.48,,,
mondo:0001430,deep corneal vascularisation,['deep vascularization of cornea'],12087,,,C0155095,,,,,370.63,,,
mondo:0001431,toxic or nutritional optic neuropathy,['nutritional optic neuropathy'],1209,,,C0155302,,,,,377.33,H46.2,,
mondo:0001433,vaginal disorder,"['vaginal disorder', 'disorder of vagina', 'vagina disease or disorder', 'vaginal disease', 'vagina disease', 'disease of vagina']",121,,,C0042251,,C26910,,D014623,,,,
mondo:0001434,inflammatory spondylopathy,"['inflammatory spondylopathies in disease EC', 'inflammatory spondylopathy in disease classified elsewhere', 'inflammatory spondylopathies in disease classified elsewhere']",12105,,,,,,,,720.9,,,
mondo:0001435,bullous retinoschisis,,12108,,,C0344289,,,,,361.12,,,
mondo:0001436,hemosiderosis,['haemosiderosis'],12119,,,C0019114,,C82892,,D006486,,,,
mondo:0001437,pulmonary alveolar proteinosis,"['pulmonary alveolar proteinosis', 'PAP']",12120,,,C0034050,,C85037,,D011649,516.0,,,
mondo:0001438,postinflammatory pulmonary fibrosis,"['postinflammatory pulmonary fibrosis', 'post-inflammatory pulmonary fibrosis']",12123,,,C0175999,,,,,515,,,
mondo:0001439,episcleritis periodica fugax,,12124,,,C0155351,,,,,379.01,,,
mondo:0001440,neurotrophic keratoconjunctivitis,,12125,,,C0155084,,,,,370.35,,,
mondo:0001441,pica disease,"['Pica', 'Pica eating disorder']",12128,,,,,C92566,,D010842,307.52,,,
mondo:0001442,dysthymic disorder,['dysthymia'],12139,,,,,C34562,0008623,D019263,300.4,F34.1,,
mondo:0001443,tympanosclerosis,,1214,,,,,,,D063371,385.09,H74.0,,
mondo:0001444,Chagas disease,"['Chagas^ disease', 'Chagas^ disease with nervous system involvement', 'Chagas^ disease with other organ involvement', 'Chagas disease', 'American trypanosomiasis', 'Trypanosoma cruzi caused disease or disorder', 'Chagas^ disease with digestive system involvement']",12140,,3386,C0348782,,C84629,0008559,D014355,086.2,B57,10001935,
mondo:0001446,low compliance bladder,"['hypertonic bladder', 'low bladder compliance', 'hypertonicity of bladder', 'hyperactivity of bladder']",12144,,,C0489967,,,,,596.52,,,
mondo:0001447,detrusor sphincter dyssynergia,"['detrusor sphincter dyssynergia', 'detrusor sphincter dyssynergia (disease)']",12145,,,C0341747,,,,,596.55,,,0025488
mondo:0001449,lymphocytic choriomeningitis,"['lymphocytic meningoencephalitis', 'lymphocytic choriomeningitis mammarenavirus caused infectious meningitis', 'LCM', 'lymphocytic choriomeningitis virus encephalomyelitis', 'lymphocytic meningitis']",12155,,,C0024266,,,,D008216,049.0,A87.2,,
mondo:0001451,peripheral retinal degeneration,"['peripheral retinal Degeneration', 'peripheral degeneration of retina']",12161,,,C1320640,,C34919,,,362.60,H35.4,,
mondo:0001452,pseudoretinitis pigmentosa,"['secondary pigmentary degeneration of retina', 'secondary pigmentary retinal degeneration']",12162,,,C2053820,,,,,362.65,,,
mondo:0001453,senile reticular retinal degeneration,['Senile reticular degeneration of retina'],12163,,,C0154857,,,,,362.64,,,
mondo:0001454,Blessig^s cysts,"['Blessig cysts', 'Microcystoid retinal degeneration', 'Iwanoff^s cysts', 'Microcystoid degeneration of retina']",12164,,,C0154855,,,,,362.62,,,
mondo:0001455,retinal lattice degeneration,['palisade degeneration of retina'],12165,,,C0154856,,,,,362.63,,,
mondo:0001456,cobblestone retinal degeneration,"['paving stone retinal degeneration', 'paving stone degeneration of retina']",12166,,,C0154854,,,,,362.61,,,
mondo:0001457,secondary vitreoretinal degeneration,,12167,,,C0154859,,,,,362.66,,,
mondo:0001458,ulnar nerve lesion,"['peripheral nerve lesion of ulnar nerve', 'lesion of ulnar nerve', 'ulnar nerve peripheral nerve lesion']",12168,,,C1288279,,,,,354.2,,,
mondo:0001459,radial neuropathy,"['radial nerve peripheral neuropathy', 'peripheral neuropathy of radial nerve']",12171,,,C0748226,,,,D020425,,,,
mondo:0001460,dyshormonogenic goiter,,12175,,,C0152077,,,,,246.1,,,
mondo:0001461,tinea corporis,"['dermatophytosis of the trunk', 'dermatophytosis of the body']",12179,,,C0546826,,,,,110.5,B35.4,,
mondo:0001462,descending colon cancer,"['malignant neoplasm of left colon', 'malignant tumour of descending colon', 'descending colon cancer', 'malignant tumor of descending colon', 'cancer of descending colon', 'malignant descending colon neoplasm', 'Ca descending colon', 'malignant neoplasm of descending colon']",12190,,,C0153435,,,,,153.2,,,
mondo:0001463,splenic flexure cancer,"['malignant tumour of splenic flexure', 'malignant neoplasm of splenic flexure of colon', 'Ca splenic flexure - colon', 'splenic flexure of colon cancer', 'malignant neoplasm of splenic flexure', 'malignant tumor of splenic flexure', 'cancer of splenic flexure of colon', 'malignant splenic flexure of colon neoplasm']",12191,,,C0153440,,,,,153.7,,,
mondo:0001464,sigmoid colon cancer,"['sigmoid colon cancer', 'Ca sigmoid colon', 'malignant sigmoid colon neoplasm', 'cancer of sigmoid colon', 'malignant neoplasm of sigmoid colon', 'malignant tumor of sigmoid colon', 'malignant tumour of sigmoid colon']",12192,,,C0153436,,,,,153.3,,,
mondo:0001465,superficial keratitis,,12196,,,C0155074,,,,,370.20,,,
mondo:0001466,punctate epithelial keratoconjunctivitis,"['Thygeson superficial punctate keratitis', 'punctate keratitis', 'Thygeson^s superficial punctate keratitis']",12197,,,C0259799,,,,,370.21,,,
mondo:0001468,synovial plica syndrome,,12225,,,C0410485,,,,,727.9,,,
mondo:0001469,cascade stomach,['hourglass stricture or stenosis of stomach'],12234,,,C0267183,,,,,537.6,,,
mondo:0001470,anal margin squamous cell carcinoma,"['squamous cell carcinoma of the anal margin', 'perianal skin squamous cell carcinoma', 'anal margin squamous cell carcinoma', 'squamous cell carcinoma of anal margin']",12239,,,C1412037,,C6925,,,173.5,,,
mondo:0001471,histoplasmosis meningitis,"['Histoplasma capsulatum caused infectious meningitis', 'histoplasmosis with meningitis']",12246,,,,,,,,115.91,,,
mondo:0001472,testicular lymphoma,"['TLYM', 'lymphoma of the testis', 'primary testicular lymphoma', 'malignant lymphoma of testis', 'lymphoma of testis', 'testicular lymphoma']",12253,,,C0349644,,C6810,,,186.9,,,
mondo:0001473,medulloadrenal hyperfunction,,12257,,,C0154206,,,,,255.6,,,
mondo:0001474,chronic salpingo-oophoritis,"['chronic salpingitis/oophoritis', 'salpingo-oophoritis, chronic', 'chronic salpingo-oophoritis', 'chronic salpingitis and oophoritis']",12265,,,C0156328,,,,,614.1,,,
mondo:0001475,neutropenia,,1227,,,C0027947,,,,D009503,288.00,,,0001875
mondo:0001476,coloboma,"['coloboma of eye', 'coloboma of macula', 'coloboma of the eye', 'ocular coloboma', 'congenital ocular coloboma']",12270,,194,,"['-0.317', '0.02939', '-0.05783', '-0.003326', '0.3242', '-0.05402', '0.06155', '0.2087', '-0.2847', '-0.2417', '-0.1516', '-0.288', '0.07086', '0.3203', '-0.3452', '-0.2832', '0.1057', '-0.04858', '-0.09174', '-0.3945', '-0.1858', '0.0423', '0.2075', '-0.1214', '0.1898', '0.0897', '-0.01906', '0.2283', '0.01688', '0.0954', '0.1276', '-0.05026', '0.1893', '0.0985', '0.0628', '0.1415', '0.2844', '-0.00818', '-0.02109', '-0.4382', '0.3423', '0.0801', '-0.06073', '-0.1865', '-0.05704', '-0.2356', '0.1109', '0.1545', '0.1371', '0.04828', '0.0548', '-0.2996', '0.01246', '-0.0557', '-0.2866', '-0.241', '0.2737', '-0.04535', '-0.2607', '-0.05722', '0.00753', '-0.04355', '0.0674', '0.3416', '-0.16', '-0.1346', '0.3076', '0.2128', '-0.1804', '0.06647', '-0.1129', '0.2727', '0.1652', '-0.081', '0.03072', '0.0734', '0.359', '0.12445', '-0.2651', '-0.1996', '-0.1332', '0.05835', '0.0927', '0.2317', '-0.1235', '-0.4119', '0.04453', '0.2133', '-0.03387', '0.0915', '-0.11224', '0.4268', '0.09875', '0.2191', '0.4973', '-0.07184', '0.1236', '-0.3486', '0.08966', '0.1284']",C98877,,D003103,743.49,,,
mondo:0001478,anisometropia,"['anisometropia', 'anisometropia (disease)']",12273,,,C0003081,,,,D015858,367.31,H52.31,,0012803
mondo:0001479,cutaneous diphtheria,['cutaneous diphtheria'],12275,,,C0012555,,C34544,1000683,,032.85,A36.3,,
mondo:0001480,malignant tumor of undescended testis,"['malignant neoplasm of retained testis', 'malignant tumour of retained testis', 'malignant neoplasm of undescended testis', 'malignant tumor of retained testis']",12276,,,C0153595,,,,,186.0,,,
mondo:0001481,femoral vein thrombophlebitis,"['phlebitis and thrombophlebitis of femoral vein (deep) (superficial)', 'phlebitis and thrombophlebitis of femoral vein', 'thrombophlebitis of the femoral vein', 'femoral vein thrombophlebitis', 'thrombophlebitis of femoral vein', 'thrombophlebitis of deep femoral vein']",12282,,,C0265066,,,,,451.11,,,
mondo:0001482,testicular leukemia,['testicular leukemia'],12286,,,C1336711,,C9277,,,,,,
mondo:0001484,paranoid schizophrenia,"['paraphrenia - late', 'paranoid type schizophrenia subchronic state', 'paraphrenic schizophrenia', 'chronic paranoid schizophrenia', 'paranoid type schizophrenia']",1229,,,,,C35006,,D012563,295.32,F20.0,,
mondo:0001485,atypical depressive disorder,['atypical depression'],12294,,,,,,,,296.82,,,
mondo:0001487,intrahepatic bile duct cancer,"['malignant neoplasm of intrahepatic biliary passages', 'malignant neoplasm of intrahepatic bile duct', 'malignant intrahepatic bile duct neoplasm', 'cancer of intrahepatic bile duct', 'Ca intrahepatic bile ducts', 'malignant neoplasm of intrahepatic bile ducts']",12298,,,C0546835,,,,,155.1,,,
mondo:0001488,anterior corneal pigmentation,['anterior corneal pigmentations'],12307,,,C0155104,,,,,371.11,,,
mondo:0001490,corneal granular dystrophy,['granular corneal dystrophy'],12318,,,C0018179,,C34651,,,371.53,H18.53,,
mondo:0001491,cough variant asthma,,12323,,,C0694548,,,,,493.82,J45.991,,
mondo:0001492,kyphoscoliotic heart disease,,12325,,,C0152102,,,,,416.1,I27.1,,
mondo:0001493,chronic pulmonary heart disease,['Cor pulmonale'],12326,,,C0238074,,C34478,,,416.9,,,
mondo:0001495,hematocele of tunica vaginalis testis,"['hematocele', 'male hematocele']",12332,,,C1456400,,,,D006398,,,,
mondo:0001496,male genital organ stricture,['stricture of male genital organs'],12333,,,,,,,,608.85,,,
mondo:0001497,male genital organ vascular disease,['vascular disorder of male genital organs'],12335,,,C0042374,,,,,608.83,,,
mondo:0001498,varicocele,"['scrotum varicose disease', 'varicose disease of scrotum', 'scrotal varices']",12337,,,C0042341,,,,D014646,456.4,I86.1,,
mondo:0001499,retroperitoneal lymphoma,"['retroperitoneal lymphoma', 'retroperitoneal space lymphoma', 'lymphoma of retroperitoneal space', 'primary retroperitoneal lymphoma']",12339,,,C1335779,,C7353,,,,,,
mondo:0001500,gender identity disorder,,1234,,,,,C94362,0008587,,302.89,,,
mondo:0001501,retroperitoneal sarcoma,"['retroperitoneal sarcoma', 'sarcoma of retroperitoneal space', 'retroperitoneal space sarcoma']",12341,,,C0585129,,C4832,,,,,,
mondo:0001502,retroperitoneum carcinoma,"['retroperitoneal space carcinoma', 'retroperitoneal cancer', 'carcinoma of retroperitoneum', 'carcinoma of the retroperitoneum', 'retroperitoneal carcinoma', 'carcinoma of retroperitoneal space']",12342,,,C0948749,,C7352,,,,,,
mondo:0001503,primary eye hypotony,['primary hypotony of eye'],12349,,,C0154782,,,,,360.31,,,
mondo:0001504,fetishistic disorder,['fetishism'],1235,,,,,C94353,,D005329,302.81,F65.0,,
mondo:0001505,alcoholic hepatitis,"['acute alcoholic hepatitis', 'alcoholic hepatitis', 'alcoholic Hepatitis', 'acute alcoholic Hepatitis', 'acute alcoholic liver disease']",12351,,,C0001306,,C34684,,D006519,571.1,K70.1,,
mondo:0001506,prostatocystitis,,12355,,,C0156291,,,,,601.3,N41.3,,
mondo:0001507,viral labyrinthitis,"['epidemic vertigo (finding)', 'epidemic vertigo', 'Viruses caused labyrinthitis']",12357,,,C0155508,,,,,386.35,,,
mondo:0001508,patulous eustachian tube,,12358,,,C0155434,,,,,381.7,H69.0,,
mondo:0001509,endocrine exophthalmos,"['thyroid eye disease', 'Graves’ eye disease', 'Graves’ orbitopathy', 'thyroid-associated ophthalmopathy', 'Graves’ ophthalmopathy', 'TED']",12359,,,C0155264,,,,,376.2,,,
mondo:0001510,lateral displacement of eye,['lateral displacement of globe'],12360,,,C0155272,,,,,376.36,,,
mondo:0001511,thyrotoxic exophthalmos,,12362,,,C0155265,,,,,376.21,,,
mondo:0001512,intermittent proptosis,['intermittent exophthalmos'],12363,,,C0155270,,,,,376.34,,,
mondo:0001513,pulsating exophthalmos,,12364,,,C0155271,,,,,376.35,,,
mondo:0001514,prolapse of urethra,['urethrocele'],12369,,,C0238502,,,,,618.03,N81.0,,
mondo:0001515,corneal degeneration,,1237,,,C0155118,,,,,371.49,H18.4,,
mondo:0001516,spinal muscular atrophy,,12377,,,C0026847,,C85075,0008525,D009134,335.19,,,
mondo:0001517,dysentery,"['infectious diarrheal disease', 'infectious diarrhoea', 'dysenteric diarrhoea', 'diarrheal disease, infectious', 'infective diarrhoea', 'infectious diarrhea', 'infectious diarrheal diseases']",12384,,,C0013369,,,1001869,D004403,009.2,,,
mondo:0001518,spastic entropion,,12395,,,C0155190,,,,,374.03,,,
mondo:0001519,entropion,"['entropion', 'entropion (disease)']",12397,,,C0014390,,,,D004774,374.00,,,0000621
mondo:0001520,kleptomania,"['kleptomania', 'pathological stealing']",12400,,,,,C94333,,,312.32,F63.2,,
mondo:0001521,intermittent explosive disorder,['explosive personality disorder'],12401,,,,,C94332,,,312.34,F63.81,,
mondo:0001522,pyromania,"['firesetting behavior', 'firesetting behaviour', 'pathological firesetting']",12402,,,,,C94334,,D005391,312.33,F63.1,,
mondo:0001523,luxation of globe,['luxation of eye'],1241,,,C0154806,,,,,360.81,,,
mondo:0001525,thyrocalcitonin secretion disease,['disorder of thyrocalcitonin secretion'],12424,,,C0701822,,,,,246.0,,,
mondo:0001526,labia minora cancer,"['cancer of labium minora', 'labium minora cancer', 'malignant neoplasm of labia minora', 'malignant tumor of labia minora', 'malignant labia minora neoplasm', 'malignant labia minora tumour', 'malignant neoplasm of labium minora', 'malignant neoplasm of labium minus', 'malignant tumour of labia minora', 'malignant neoplasm of the labia minora', 'malignant tumor of the labia minora', 'malignant tumour of the labia minora', 'malignant labium minora neoplasm', 'malignant labia minora tumor']",1243,,,C0496815,,C7637,,,184.2,C51.1,,
mondo:0001527,conjugate gaze palsy,['palsy of conjugate gaze'],12445,,,C0702143,,,,,378.81,,,
mondo:0001528,vulva cancer,"['vulvar tumour', 'vulval neoplasm', 'malignant mammalian vulva neoplasm', 'malignant neoplasm of vulva, unspecified', 'malignant neoplasm of vulva', 'malignant tumour of the vulva', 'vulval cancer', 'malignant vulva tumour', 'malignant tumor of the vulva', 'malignant vulva neoplasm', 'malignant vulvar neoplasm', 'neoplasm of vulva', 'malignant vulvar tumor', 'Ca vulva', 'malignant vulva tumor', 'malignant neoplasm of the vulva', 'vulvar cancer', 'malignant tumour of vulva', 'malignant vulvar tumour', 'cancer of mammalian vulva', 'mammalian vulva cancer', 'malignant neoplasm of vulva unspecified', 'malignant neoplasm of mammalian vulva', 'malignant tumor of vulva']",1245,,,,,C7502,,D014846,184.4,,,
mondo:0001529,pancytopenia,,12450,,,C0030312,,C34889,,D010198,284.89,,,
mondo:0001530,secondary hyperparathyroidism of renal origin,"['hyperparathyroidism due to renal insufficiency', 'secondary hyperparathyroidism (of renal origin)']",12465,,,C0271847,,,,,588.81,N25.81,,
mondo:0001531,blood coagulation disease,"['blood coagulation disorder', 'coagulation disorder', 'disorder, blood coagulation', 'coagulation defect', 'postpartum coagulation defect', 'postpartum coagulation defect with delivery', 'coagulation disorder, blood', 'coagulopathy', 'coagulation disorders, blood', 'disorders, blood coagulation']",1247,,,,,C2902,,D001778,287.8,,,
mondo:0001532,capillariasis,"['Capillaria infection', 'infections, Capillaria']",12474,,,C0006897,,,,,127.5,,,
mondo:0001533,pes anserinus tendinitis or bursitis,,12475,,,,,,,,726.61,,,
mondo:0001534,ocular hyperemia,"['hyperemia of conjunctiva', 'hyperemia eye']",1248,,,C0155169,,,,,,,,
mondo:0001535,vagus nerve disorder,"['vagus nerve disease or disorder', 'Vagus nerve disorder', 'disorder of vagus nerve', 'disorder of vagal nerve', 'disorder of pneumogastric [10th] nerve', 'disease of vagus nerve', 'vagus nerve disease']",12491,,,C0152179,,C27591,,D020421,352.3,,,
mondo:0001536,vaginal leiomyoma,"['leiomyoma of the vagina', 'leiomyoma of vagina', 'vagina leiomyoma', 'vaginal leiomyoma']",125,,,C1336939,,C6373,,,,,,
mondo:0001537,tuberculous epididymitis,,1251,,,C0152814,,,,,016.46,,,
mondo:0001538,retinal ischemia,"['retina ischemic disease', 'ischemic disease of retina', 'ischaemic disease of retina', 'retina ischaemic disease']",12510,,,C0162291,,,,,362.84,H35.82,,
mondo:0001539,retinal perforation,"['retinal break', 'retinal tear', 'retinal dialysis']",12514,,,C0035321,,,,D012167,,,,
mondo:0001540,bagassosis,"['bagasse workers lung', 'sugar cane worker pneumonitis', 'bagasse extrinsic allergic alveolitis']",12522,,,C0004681,,C34409,,D011009,495.1,J67.1,,
mondo:0001541,plantar nerve lesion,"['plantar nerve peripheral nerve lesion', 'lesion of plantar nerve']",12524,,,C0154752,,,,,355.6,,,
mondo:0001542,common peroneal nerve lesion,"['common fibular nerve peripheral nerve lesion', 'peripheral nerve lesion of common fibular nerve']",12527,,,C0270909,,,,,355.3,,,
mondo:0001543,lesion of sciatic nerve,"['peripheral nerve lesion of sciatic nerve', 'sciatic nerve peripheral nerve lesion']",12528,,,C0154748,,,,,355.0,G57.0,,
mondo:0001544,tibial nerve palsy,,12529,,,C0154751,,,,,355.8,,,
mondo:0001546,hypermobility of coccyx,"['coccygeal hypermobility syndrome', 'hypermobility of the coccyx']",12537,,,C0158295,,,,,724.71,,,
mondo:0001547,atrophic nonflaccid tympanic membrane,,12546,,,C0155471,,,,,384.82,,,
mondo:0001548,hepatic coma,['hepatocerebral intoxication'],12550,,,C0019147,,,,,070.42,,,
mondo:0001549,hemolytic-uremic syndrome,"['hemolytic uremic syndrome', 'acute renal failure, thrombocytopenia, and microangiopathic hemolytic anemia associated with distorted erythrocytes (^burr cells^)', 'HUS', 'haemolytic-uraemic syndrome', 'acute renal failure, thrombocytopenia, and microangiopathic hemolytic anaemia associated with distorted erythrocytes (^burr cells^)']",12554,,576742,C0019061,,C75545,,D006463,283.11,D59.3,,
mondo:0001551,ulceration of vulva,,12566,,,C0156339,,,,,616.51,N76.6,,
mondo:0001552,dyscalculia,"['mathematics disorder', 'disorder of arithmetical skills', 'dyscalculia', 'dyscalculia (disease)']",12568,,,,,C97165,,D060705,315.1,,,0002442
mondo:0001553,phacolytic glaucoma,,12570,,,C0152137,,,,,365.51,,,
mondo:0001554,phacogenic glaucoma,['phacomorphic glaucoma'],12571,,,C0339590,,,,,365.59,,,
mondo:0001555,neonatal thyrotoxicosis,['infantile hyperthyroidism'],12573,,,C0158983,,C114906,,,775.3,,,
mondo:0001556,urethral obstruction,"['obstruction of urethra', 'urethral obstruction (disease)', 'urethral obstruction']",12577,,,C0041972,,,,D014524,599.69,,,0000796
mondo:0001557,olecranon bursitis,"['bursitis of elbow region', 'capped elbow', 'olecranon bursitis', 'bursitis of olecranon', 'bursitis of elbow', 'miner^s elbow', 'shoe boil', 'elbow bursitis', 'Miners^ elbow', 'elbow bursitis (& olecranon)']",12581,,,C3887895,,,,,726.33,M70.2,,
mondo:0001558,Potter sequence,"['Potter^s syndrome', 'oligohydramnios sequence', 'Potter syndrome', 'Potter^s sequence']",12594,,,C0178426,,C40435,,,,Q60.6,,
mondo:0001559,perineocele,,12637,,,,,,,,618.05,N81.81,,
mondo:0001560,hypertrophic pyloric stenosis,"['IHPS', 'congenital or infantile stricture of pylorus', 'infantile pyloric stenosis', 'congenital constriction of the pylorus', 'infantile hypertrophic pyloric stenosis', 'congenital pyloric stenosis', 'congenital hypertrophic pyloric stenosis', 'infantile Hypertrophy of the pylorus', 'infantile stricture of the pylorus', 'pyloric stenosis, infantile', 'congenital Hypertrophy of the pylorus', 'congenital stricture of the pylorus', 'infantile constriction of the pylorus']",12638,,,,,C98952,0004707,D046248,750.5,Q40.0,,
mondo:0001561,pyloric stenosis,"['gastric outflow obstruction', 'pyloric stenosis', 'GOO', 'gastric outlet obstruction', 'pyloric stenosis (disease)']",3122,,,,,C34966,1000947,D017219,,,10062499,0002021
mondo:0001562,displacement of cardia through esophageal hiatus,['congenital hiatus hernia'],12641,,,,,,,,750.6,Q40.1,,
mondo:0001563,vestibulocochlear nerve disorder,"['disorder of vestibulocochlear nerve', 'vestibulocochlear nerve disease or disorder', 'vestibulocochlear nerve disorder', 'acoustic nerve disorder NOS', 'disease of vestibulocochlear nerve', 'vestibulocochlear nerve disease', 'acoustic nerve disease', 'acoustic nerve disorder']",12657,,,C0001163,,C27207,,D000160,388.5,,,
mondo:0001564,binocular vision disease,"['binocular vision disorder', 'simultaneous visual perception without fusion']",12667,,,,,C34422,,,368.30,,,
mondo:0001565,abnormal retinal correspondence,,12668,,,C0155010,,,,,368.34,H53.31,,
mondo:0001566,hypercalcemia disease,['hypercalcemia'],12678,,,C0020437,,C3112,,D006934,275.42,E83.52,,0003072
mondo:0001567,nephrocalcinosis,['hypercalcemic nephropathy'],12679,,,C0027709,,C84918,,D009397,275.49,,,
mondo:0001568,mixed receptive-expressive language disorder,,12685,,,,,C92563,,,315.32,F80.2,,
mondo:0001569,acoustic neuroma,"['vestibular schwannoma', 'acoustic neurinoma', 'acoustic tumor', 'acoustic neuroma', 'neurilemoma, acoustic', 'neuroma, acoustic', 'acoustic tumour', 'vestibular schwannoma (disease)', 'acoustic schwannoma', 'vestibular neurilemmoma', 'acoustic neurilemmoma', 'neurinoma of the acoustic nerve', 'acoustic neurilemoma']",12689,,252175,,,C3276,,D009464,,,10000523,0009588
mondo:0001571,gynecomastia disorder,['male organism hypertrophy of breast'],12698,,,C0018418,,C3073,,D006177,,,,0000771
mondo:0001572,leiomyoma,"['fibroid neoplasm', 'fibroid tumour', 'fibroid', 'leiomyoma', 'leiomyoma, benign', 'leiomyomatous tumour', 'leiomyomatous neoplasm', 'leiomyomatous tumor', 'fibroid tumor', 'leiomyomatous neoplasm (morphologic abnormality)']",127,,,C0023267,,C3157,,D007889,215.9,,,
mondo:0001574,capillary disorder,"['disease of capillary', 'disease of capillaries', 'disorder of capillary', 'capillary disease or disorder', 'capillary disease']",1271,,,C0155765,,,,,448.9,,,
mondo:0001575,chronic gonococcal salpingitis,"['gonococcal salpingitis', 'gonococcal salpingitis, chronic']",12718,,,C0153208,,,,,098.37,,,
mondo:0001576,telangiectasis,['telangiectasia'],1272,,,C0039446,,C28194,,D013684,,,,
mondo:0001577,respiratory syncytial virus infectious disease,"['Human respiratory syncytial virus infection', 'infections, Human respiratory syncytial virus', 'respiratory syncytial virus infection']",1273,,,C0035235,,C3354,1001413,D018357,,,,
mondo:0001579,corneal staphyloma,,12753,,,C0152440,,,,,371.73,,,
mondo:0001580,lacrimal duct cancer,"['malignant neoplasm of lacrimal duct', 'malignant lacrimal duct tumour', 'cancer of lacrimal drainage system', 'malignant lacrimal duct neoplasm', 'malignant neoplasm of the lacrimal duct', 'malignant tumor of the lacrimal duct', 'malignant tumour of lacrimal duct', 'malignant tumor of lacrimal duct', 'lacrimal drainage system cancer', 'malignant neoplasm of lacrimal drainage system', 'malignant lacrimal drainage system neoplasm', 'malignant tumour of the lacrimal duct', 'malignant lacrimal duct tumor']",12756,,,C0153631,,C3567,,,190.7,,,
mondo:0001582,cicatricial ectropion,,12782,,,C0155196,,,,,374.14,,,
mondo:0001583,diabetic polyneuropathy,"['diabetes mellitus with polyneuropathy', 'polyneuropathy in diabetes']",12785,,,C0271680,,,,,357.2,,,
mondo:0001584,ocular motility disease,"['eye movement disorder', 'disorder of eye movements']",1279,,,,,,1001990,,378.9,,,
mondo:0001585,hallucinogen abuse,,12797,,,,,,,,305.3,,,
mondo:0001586,mucopolysaccharidosis type 1,"['MPSI', 'severe MPS I (subtype, also known as Hurler syndrome)', 'iduronidase deficiency disease', 'MPS I', 'mucopolysaccharidosis, type 1', 'MPS 1', 'Alpha-L-iduronidase deficiency', 'mucopolysaccharidosis type I', 'lipochondrodystrophy', 'IDUA deficiency', 'MPS I - Hurler syndrome', 'mucopolysaccharidosis type 1', 'Hurler-Scheie syndrome (subtype)', 'Scheie syndrome (subtype) formerly known as Mucopoly-saccharidosis type V)', 'Hurler syndrome', 'mucopolysaccharidosis I', 'Hurler syndrome (subtype)', 'MPS1', 'attenuated MPS I (subtype, includes Hurler-Scheie and Scheie syndrome)', 'mucopolysaccharidosis, MPS-I']",12802,,579,,"['0.2817', '0.664', '0.03528', '-0.412', '0.1815', '0.00807', '0.1678', '0.676', '-0.325', '-0.625', '-0.1439', '0.002731', '0.2559', '0.784', '0.1558', '-0.63', '0.1565', '-0.5713', '-0.03055', '-0.3381', '0.09357', '-0.1788', '0.736', '-0.1539', '0.2057', '-0.2969', '0.3', '0.3052', '0.1699', '0.3813', '0.675', '0.2462', '0.272', '0.1045', '-0.1111', '-0.63', '-0.0669', '-0.6724', '0.574', '-0.0699', '0.2367', '-0.641', '0.2737', '0.3955', '0.1846', '0.409', '-0.1409', '-0.3484', '-0.1744', '-0.03284', '0.2224', '-0.02806', '0.0895', '-0.2163', '0.1322', '-0.7324', '-0.2683', '-0.003736', '0.2343', '0.2367', '0.2961', '-0.228', '-0.1831', '-0.1053', '0.1431', '-0.2893', '0.311', '-0.4924', '-0.3853', '-0.07635', '-0.819', '-0.4038', '-0.157', '-0.6196', '0.4006', '0.4316', '-0.4595', '0.02264', '-0.6655', '-0.2527', '-0.2507', '-0.512', '-0.351', '0.9727', '-0.736', '0.1589', '0.4802', '0.1879', '0.331', '-0.01021', '0.22', '0.3855', '-0.05136', '0.08514', '0.3435', '0.3467', '-0.1045', '-0.7046', '0.5234', '-0.1327']",C85053,,,,,10056886,
mondo:0001588,chronic lacrimal gland enlargement,['chronic enlargement of lacrimal gland'],12809,,,C1300133,,,,,375.03,,,
mondo:0001590,quadriplegia,"['tetraplegia', 'bilateral diplegia']",12835,,,C0034372,,C50721,,D011782,344.09,,,
mondo:0001591,senile entropion,['involutional entropion'],12836,,,C0155188,,,,,374.01,,,
mondo:0001592,prolapse of female genital organ,,1284,,,C0156349,,,,,618.89,N81,,
mondo:0001593,rectal disorder,"['rectum disease', 'rectum disease or disorder', 'disorder of rectum', 'disease of rectum']",1285,,,C0034882,,,,D012002,569.49,,,
mondo:0001594,Achilles bursitis,"['Achilles bursitis or tendinitis', 'Haglund^s disease', 'Haglund^s deformity', 'capped hock']",12857,,,C0149846,,,,,726.71,,,
mondo:0001595,choreatic disease,"['hereditary benign chorea', 'chorea, benign hereditary', 'benign familial chorea', 'BHC', 'hereditary chorea', 'hereditary progressive chorea without dementia', 'Bch']",12859,,1429,,"['-0.2153', '0.4016', '0.1715', '-0.2837', '-0.2303', '-0.3096', '0.2864', '0.0733', '-0.621', '-0.1272', '0.05508', '0.2014', '0.0751', '0.06274', '0.4993', '0.2678', '-0.0653', '-0.2627', '-0.0182', '-0.837', '-0.04742', '0.09625', '0.1892', '-0.1566', '-0.1707', '-0.02797', '-0.004734', '-0.3186', '-0.132', '-0.1348', '0.1539', '-0.002878', '0.2637', '0.1912', '0.2284', '0.1616', '-0.4165', '-0.1772', '-0.1685', '-0.1456', '0.3772', '-0.4539', '-0.2668', '0.2542', '0.4497', '-0.5176', '-0.0705', '0.3464', '0.2915', '0.614', '-0.537', '0.662', '-0.1115', '-0.2399', '0.5645', '-0.4653', '0.1002', '-0.1274', '0.03058', '-0.1111', '-0.144', '0.02235', '0.2229', '-0.2108', '-0.452', '0.3167', '0.1866', '0.319', '-0.202', '0.2057', '-0.08575', '-0.1344', '-0.04767', '0.11536', '-0.006363', '0.542', '0.1384', '0.12494', '-0.01298', '-0.2252', '0.134', '-0.416', '0.3894', '0.376', '0.359', '-0.2188', '0.007607', '0.0871', '0.6465', '0.116', '0.1849', '0.37', '-0.0528', '0.3516', '0.5244', '0.4155', '0.2433', '0.3782', '0.255', '0.286']",C84633,0004152,D002819,333.5,,,0002072
mondo:0001596,hypochondriasis,"['hypochondria', 'hypochondriacal disorder', 'hypochondriacal neurosis']",12883,,,,,,,D006998,300.7,,,
mondo:0001597,submandibular gland disorder,"['disease of submandibular gland', 'disorder of submandibular gland', 'submandibular gland disease', 'submandibular gland disease or disorder']",12897,,,C0038557,,,,D013364,,,,
mondo:0001598,benign lymphoepithelial lesion of salivary gland,"['benign lymphoepithelial lesion of the salivary gland', 'Godwin tumour', 'benign lymphoepithelial lesion of salivary gland', 'benign salivary gland lymphoepithelial lesion', 'Godwin tumor']",12899,,,C0266995,,C3949,,,527.8,,,
mondo:0001600,mucocele of salivary gland,"['salivary cyst', 'salivary gland mucocele', 'ranula', 'mucous retention cyst of salivary gland']",12904,,,C2242813,,,,D011900,527.6,K11.6,,
mondo:0001601,Plasmodium ovale malaria,"['ovale malaria', 'Malariaby Plasmodium ovale']",12919,,,C0152072,,,,,084.3,B53.0,,
mondo:0001602,labia minora carcinoma,"['carcinoma of labium minora', 'labium minora carcinoma', 'labia minora cancer', 'carcinoma of the labia minora', 'carcinoma of labia minora', 'labia minora carcinoma']",1293,,,C1334357,,C9364,,,,,,
mondo:0001603,paralytic lagophthalmos,"['paralytic lagophthalmos', 'paralytic lagophthalmos (disease)']",12958,,,C0155197,,,,,374.21,,,0030003
mondo:0001604,lagophthalmos,,12959,,,C0152226,,,,,374.20,H02.2,,
mondo:0001606,central nervous system leukemia,"['leukaemia of CNS', 'leukemia of CNS', 'leukemia of central nervous system', 'central nervous system leukaemia (disease)', 'leukaemia (disease) of central nervous system', 'leukemia of the CNS', 'leukaemia of the CNS', 'CNS leukaemia', 'leukemia of the central nervous system', 'leukaemia of the central nervous system', 'leukaemia of central nervous system', 'central nervous system leukemia', 'central nervous system leukemia (disease)', 'CNS leukemia']",12969,,,C1332884,,C5440,,,,,,
mondo:0001607,intrapelvic lymph node leukemic reticuloendotheliosis,"['leukemic reticuloendotheliosis involving intrapelvic lymph nodes', 'leukemic reticuloendotheliosis of intrapelvic lymph nodes']",12972,,,C0153831,,,,,202.46,,,
mondo:0001608,vagus nerve neoplasm,"['neoplasm of vagus nerve', 'tumor of tenth cranial nerve', 'tenth cranial nerve tumours', 'tumour of the Vagus nerve', 'tumour of Vagus nerve', 'Vagus nerve tumours', 'tumor of the tenth cranial nerve', 'neoplasm of the tenth cranial nerve', 'tenth cranial nerve neoplasm', 'neoplasm of Vagus nerve', 'vagus nerve tumor', 'neoplasm of tenth cranial nerve', 'tenth cranial nerve neoplasms', 'tumor of the Vagus nerve', 'tumour of tenth cranial nerve', 'neoplasm of the Vagus nerve', 'tenth cranial nerve tumors', 'tenth cranial nerve tumour', 'tumor of vagus nerve', 'Vagus nerve neoplasm', 'tumor of Vagus nerve', 'vagus nerve neoplasm (disease)', 'Xth cranial nerve tumours', 'Vagus nerve neoplasms', 'Xth cranial nerve tumors', 'tumour of the tenth cranial nerve', 'Xth cranial nerve neoplasms', 'vagus nerve tumour', 'tenth cranial nerve tumor', 'tumour of vagus nerve', 'Vagus nerve tumour', 'Vagus nerve tumors', 'Vagus nerve tumor']",12984,,,C1263901,,C5831,,,239.7,,,
mondo:0001609,agranulocytosis,"['Granulopenia', 'Granulocytopenic disorder', 'granulocytopenia']",12987,,,C0001824,,C2863,,D000380,288.8,D70,,
mondo:0001610,acute dacryocystitis,"['dacryocystitis, acute', 'dacryocystitis - acute']",12996,,,C0155237,,,,,375.32,,,
mondo:0001611,phlegmonous dacryocystitis,,12997,,,C0155238,,,,,375.33,H04.31,,
mondo:0001612,carotid stenosis,"['stenosis, carotid artery', 'carotid artery stenosis']",13001,,,C0007282,,C95804,,D016893,433.10,,,0100546
mondo:0001613,vertebrobasilar insufficiency,"['vertebrobasilar artery syndrome', 'vertebrobasilar insufficiency', 'vertebro-basilar insufficiency', 'vertebrobasilar arterial insufficiency']",13003,,,C0042568,,,1001449,D014715,435.3,,,
mondo:0001614,intra-abdominal lymph node mast cell malignancy,"['malignant mast cell tumours involving intra-abdominal lymph nodes', 'mast cell malignancy of intra-abdominal lymph nodes', 'malignant mast cell tumors involving intra-abdominal lymph nodes']",13005,,,C0153844,,,,,202.63,,,
mondo:0001615,epidemic keratoconjunctivitis,"['shipyard eye', 'EKC']",13014,,,C0014493,,C34590,,,077.1,,,
mondo:0001616,lobomycosis,"['cutaneous lobomycosis', 'infection by Loboa loboi', 'cutaneous blastomycosis']",13026,,,C0152066,,,1001805,D060368,116.2,B48.0,,
mondo:0001617,transient global amnesia,"['transient global amnesia (disease)', 'transient global amnesia']",13027,,,,,C85198,,D020236,437.7,G45.4,,0010534
mondo:0001618,balanoposthitis,,13031,,,C0004691,,,,,607.1,N47.6,,
mondo:0001620,louse-borne relapsing fever,"['Relapsing fever, louse-borne']",13035,,,C0152061,,C128426,,,087.0,A68.0,,
mondo:0001621,tick-borne relapsing fever,"['Relapsing fever, tick-borne']",13036,,,C0035022,,C34976,,,087.1,A68.1,,
mondo:0001622,mechanical lagophthalmos,,13037,,,C0155198,,,,,374.22,H02.22,,
mondo:0001623,cicatricial lagophthalmos,"['cicatricial lagophthalmos', 'cicatricial lagophthalmos (disease)']",13038,,,C0155199,,,,,374.23,H02.21,,0030004
mondo:0001624,acute sphenoidal sinusitis,"['sphenoidal sinus -acute', 'sphenoid sinusitis, acute', 'acute sphenoid sinusitis']",13046,,,C0155807,,,,,461.3,J01.3,,
mondo:0001625,corpus luteum cyst,['corpus luteum ovarian cyst (disease)'],13050,,,,,,,,620.1,N83.1,,
mondo:0001626,traumatic glaucoma,['glaucoma associated with ocular trauma'],13060,,,C0339594,,,,,365.65,,,
mondo:0001627,dementia,"['dementia (disease)', 'dementia']",1307,,,,,C4786,,D003704,294.8,,,
mondo:0001628,tinea unguium,"['cellulitis and abscess', 'onychomycosis due to dermatophyte', 'cellulitis and abscess of trunk', 'cellulitis and abscess of finger', 'nail dermatophytosis', 'cellulitis and abscess of buttock', 'cellulitis and abscess of upper arm and forearm', 'dermatophytosis of nail', 'cellulitis and abscess of face', 'cellulitis and abscess of gluteal region', 'dermatophytic onychomycosis', 'tinea unguium', 'dermatophytic onychia', 'onychomycosis', 'cellulitis and abscess of finger and toe']",13074,,,C4082762,,C112214,,D014009,681.9,B35.1,,
mondo:0001629,Jaccoud syndrome,"['Jaccoud^s syndrome', 'Jaccoud syndrome']",13080,,,C0152084,,,,,714.4,,,
mondo:0001630,branch retinal artery occlusion,"['retinal arterial branch occlusion', 'arterial retinal branch occlusion']",13094,,,C0006123,,C34436,,,362.32,,,
mondo:0001631,vertebral artery insufficiency,['vertebral artery syndrome'],13095,,,C0042560,,C35123,,D014715,435.1,,,
mondo:0001632,intracranial arteriosclerosis,,13097,,,C0007771,,,,D002537,,,,
mondo:0001633,central retinal artery occlusion,['central retinal arterial occlusion'],13098,,,C0007688,,C34456,,,362.31,H34.1,,
mondo:0001634,bladder leiomyoma,"['urinary bladder leiomyoma', 'leiomyoma of bladder', 'bladder leiomyoma', 'leiomyoma of urinary bladder', 'leiomyoma of the urinary bladder', 'leiomyoma of the bladder']",13109,,,C1332560,,C6178,,,,,,
mondo:0001635,bladder squamous papilloma,['bladder squamous papilloma'],13110,,,C1511199,,C39834,,,,,,
mondo:0001636,mechanical entropion,,13112,,,C0155189,,,,,374.02,,,
mondo:0001637,cicatricial entropion,,13113,,,C0155191,,,,,374.04,,,
mondo:0001638,protein-deficiency anemia,"['anemia due to protein deficiency', 'anaemia due to protein deficiency']",13120,,,C0154290,,,,,281.4,D53.0,,
mondo:0001639,deficiency anemia,"['unspecified deficiency anemia', 'unspecified deficiency anaemia', 'deficiency anemias']",13121,,,C0041782,,,,,281.9,,,
mondo:0001640,gonococcal spondylitis,,13127,,,C0153219,,,,,098.53,,,
mondo:0001641,severe pre-eclampsia,"['antepartum severe pre-eclampsia', 'severe pre-eclampsia, with delivery', 'Preeclampsia with severe features', 'postpartum severe pre-eclampsia', 'severe preeclampsia']",13129,,,,,C112843,,,642.50,,,
mondo:0001642,hordeolum externum,['external stye'],13134,,,C0019919,,,,,373.11,,,
mondo:0001643,exophthalmic ophthalmoplegia,,13135,,,C0152135,,,,,376.22,,,
mondo:0001644,acute proliferative glomerulonephritis,"['proliferative glomerulonephritis, acute', 'post-streptococcal glomerulonephritis', 'acute glomerulonephritis with lesion of proliferative glomerulonephritis']",13138,,,C0403414,,C35443,,,580.0,,,
mondo:0001645,crescentic glomerulonephritis,"['crescentic glomerulonephritis', 'crescentic glomerulonephritis (disease)']",13139,,,,,C35444,,,580.4,,,0008653
mondo:0001646,benign secondary hypertension,,13143,,,C0155620,,,,,405.19,,,
mondo:0001647,benign renovascular hypertension,,13145,,,,,,,,405.11,,,
mondo:0001648,esophageal candidiasis,"['esophageal moniliasis', 'candidiasis of the esophagus', 'esophageal thrush', 'Candida esophagitis', 'candidal esophagitis', 'candidiasis of the oesophagus']",13146,,,C0239295,,C27027,,,112.84,B37.81,,
mondo:0001649,fungal esophagitis,['fungal esophagitis'],13147,,,C0341109,,C27107,,,117.9,,,
mondo:0001650,acute cystitis,"['acute cystitis', 'acute cystitis (disease)', 'cystitis, acute']",13148,,,C0149523,,C26934,,,595.0,N30.0,,
mondo:0001651,scrotum squamous cell carcinoma,"['scrotal squamous cell carcinoma', 'squamous cell carcinoma of the scrotum', 'scrotum squamous cell carcinoma', 'squamous cell carcinoma of scrotum']",13159,,,C0349551,,C4643,,,,,,
mondo:0001652,scrotum melanoma,"['scrotum melanoma (disease)', 'melanoma of the scrotum', 'melanoma of scrotum', 'scrotal melanoma']",13160,,,C1331544,,C7361,,,,,,
mondo:0001653,prepuce cancer,"['malignant tumour of foreskin', 'malignant prepuce neoplasm', 'prepuce cancer', 'cancer of prepuce', 'malignant neoplasm of foreskin', 'malignant neoplasm of prepuce', 'malignant tumor of foreskin']",13168,,,C0153598,,,,,187.1,,,
mondo:0001654,spermatic cord cancer,"['malignant tumor of the spermatic cord', 'malignant spermatic cord tumour', 'malignant tumour of the spermatic cord', 'malignant tumor of spermatic cord', 'spermatic cord cancer', 'malignant spermatic cord neoplasm', 'malignant spermatic cord tumor', 'spermatic cord Ca', 'malignant neoplasm of the spermatic cord', 'malignant neoplasm of spermatic cord', 'malignant tumour of spermatic cord', 'cancer of spermatic cord']",13169,,,C0153603,,C3559,,,187.6,,,
mondo:0001655,dissociated nystagmus,['dissociated nystagmus'],13174,,,C0155380,,,,,379.55,H55.04,,
mondo:0001656,megaesophagus,,13186,,,C0025164,,C34811,,,,,,
mondo:0001657,brain cancer,"['cancer of brain', 'malignant neoplasm of brain', 'tumour of the brain', 'malignant tumour of brain', 'primary brain tumour', 'BT - brain tumor', 'malignant tumor of brain', 'adult malignant brain neoplasm', 'malignant primary brain neoplasm', 'malignant primary brain tumour', 'malignant brain neoplasm', 'tumor of the brain', 'malignant brain tumor', 'malignant tumour of the brain', 'primary malignant neoplasm of brain', 'brain cancer', 'cancer of the brain', 'malignant tumor of the brain', 'malignant primary brain tumor', 'brain neoplasm, adult', 'primary brain tumor', 'brain tumor, adult', 'neoplasm of unspecified nature of brain', 'brain neoplasm', 'adult brain tumour', 'adult brain tumor', 'malignant tumor of adult brain', 'malignant neoplasm of the brain', 'malignant tumour of adult brain', 'brain neoplasms, malignant', 'malignant brain tumour', 'BT - brain tumour', 'primary brain neoplasm']",1319,,,,,C4952,,D001932,239.6,,,
mondo:0001658,nontoxic goiter,"['goiter, non-toxic', 'non-toxic simple goiter', 'nontoxic goiter', 'euthyroid goiter', 'non-toxic goiter', 'euthyroid goitre', 'Nodule-thyroid, non tox', 'non-toxic simple goitre', 'non-toxic goitre']",13195,,,C0221777,,C35271,,,,,,
mondo:0001660,proliferative diabetic retinopathy,,13207,,,C0154830,,C84457,,,362.02,,,
mondo:0001661,background diabetic retinopathy,"['non proliferative diabetic retinopathy', 'non-proliferative diabetic retinopathy']",13208,,,C0004606,,C35668,,,362.03,,,
mondo:0001663,hole retinal cyst,"['macular pseudohole retinal cyst', 'macular cyst or hole', 'macular cyst, hole, or pseudohole of retina']",13214,,,C1261331,,,,,362.54,,,
mondo:0001664,submucous uterine fibroid,['submucous leiomyoma of uterus'],13222,,,C0153993,,,,,218.0,D25.0,,
mondo:0001665,oculoglandular tularemia,,13226,,,C0152944,,,,,021.3,A21.1,,
mondo:0001666,retinal dystrophies primarily involving Bruch^s membrane,"['retinal dystrophies primarily involving Bruch membrane', 'Bruch^s membrane inherited retinal dystrophy']",13227,,,,,,,,362.77,,,
mondo:0001667,streptobacillus infectious disease,,,,,C0947939,,,,,,,,
mondo:0001668,internal pathological resorption of tooth,['internal pathological resorption'],13239,,,,,,,,521.41,,,
mondo:0001670,tooth resorption,,13240,,,C0040451,,,,D014091,521.4,,,
mondo:0001671,mucocele of appendix,"['appendiceal mucocele', 'Appendicele mucocele', 'mucocele of the appendix']",13248,,,C0026684,,C3241,,,543.9,,,
mondo:0001672,bronchus cancer,"['malignant bronchus neoplasm', 'malignant neoplasm of bronchus and lung', 'malignant neoplasm of bronchus or lung', 'malignant neoplasm of bronchus and lung, unspecified', 'malignant neoplasm of bronchus', 'bronchus cancer', 'cancer of bronchus']",1325,,,,,,,,162.9,,,
mondo:0001673,diarrheal disease,"['diarrhea', 'loose stools', 'diarrhoea of presumed infectious origin', 'diarrhea of presumed infectious origin', 'frequent stools', 'diarrhoea']",13250,,,C0013369,"['0.3694', '0.2183', '0.425', '0.252', '-0.4465', '-0.7363', '-0.886', '0.4016', '-0.01936', '0.05396', '0.541', '0.556', '0.1648', '0.9946', '-1.032', '0.1654', '-0.3677', '0.204', '-0.6997', '-0.773', '0.03473', '-0.3242', '-0.2817', '-0.1019', '0.008766', '-0.6846', '-0.8506', '0.4128', '0.396', '-0.8467', '-0.3875', '-0.5957', '-0.2045', '0.435', '0.8438', '0.6543', '-0.667', '0.3818', '-0.04034', '-0.05542', '-0.5405', '-0.4177', '-0.518', '-0.5513', '0.627', '-0.0839', '0.05692', '0.1927', '-0.01683', '1.226', '-0.599', '-0.1048', '-0.02528', '-0.2512', '0.02275', '-0.3145', '-0.0853', '0.1317', '-0.6978', '-0.1934', '0.4873', '0.66', '0.318', '-0.4324', '0.1626', '-0.1357', '0.4023', '-0.2654', '0.05234', '1.1875', '-0.2417', '0.7603', '0.1975', '-0.8853', '0.7715', '0.2966', '-0.7593', '0.2576', '0.0852', '0.5874', '-0.3577', '-0.7153', '-0.4111', '0.148', '0.306', '0.425', '0.526', '0.09875', '0.051', '-0.2322', '-0.3362', '-0.2043', '-0.2656', '-0.3872', '0.8022', '0.851', '0.1056', '-1.747', '-0.2957', '-0.2382']",C2987,,D003967,009.2,,,0002014
mondo:0001674,diverticulitis of colon,"['colon diverticulitis', 'colonic diverticular disease']",13254,,,C0012814,,,,D004239,562.12,,,
mondo:0001676,erythropoietic protoporphyria,"['protoporphyria', 'EPP (erythropoietic protoporphyria porphyria)']",13270,,,,,,,D046351,,,,
mondo:0001678,intestinal tuberculosis,"['intestine tuberculosis', 'tuberculosis of intestine']",13282,,,C0275911,,,,,014.80,,,
mondo:0001680,vaginal mullerian papilloma,"['vaginal Muellerian papilloma', 'vaginal Müllerian papilloma', 'vaginal Mullerian papilloma']",133,,,C1519926,,C40255,,,,,,
mondo:0001681,diphtheritic cystitis,,13306,,,C0152954,,,,,032.84,A36.85,,
mondo:0001682,diphtheritic peritonitis,,13310,,,C0152953,,,,,032.83,,,
mondo:0001683,pancreatic mucinous ductal ectasia,,13313,,,C1335310,,C5717,,,,,,
mondo:0001684,exocrine pancreatic insufficiency,"['exocrine pancreatic insufficiency', 'exocrine pancreas insufficiency', 'pancreatic insufficiency']",13316,,,C0267963,,C84316,,D010188,577.8,K86.81,,
mondo:0001685,chronic follicular conjunctivitis,,13326,,,C0155147,,,,,372.12,,,
mondo:0001686,anatomical narrow angle borderline glaucoma,,13327,,,,,,,,365.02,,,
mondo:0001687,diabetic cataract,['cataract - diabetic'],13328,,,C0011876,,,,,366.41,,,
mondo:0001688,toxic optic neuropathy,,13329,,,C0155303,,,,D000081028,377.34,H46.3,,
mondo:0001689,hypertrophy of tongue papillae,['tongue papillary hypertrophy'],13333,,,C0392494,,,,,529.3,K14.3,,
mondo:0001690,parasitic conjunctivitis,,13341,,,C0155148,,,,,372.15,,,
mondo:0001691,laryngeal cartilage cancer,"['malignant neoplasm of laryngeal cartilage', 'malignant tumor of laryngeal cartilage', 'malignant tumour of laryngeal cartilage', 'laryngeal cartilage cancer', 'cancer of laryngeal cartilage', 'malignant neoplasm of laryngeal cartilages', 'malignant laryngeal cartilage neoplasm']",13348,,,C0153486,,,,,161.3,,,
mondo:0001692,pedophilia,['Paedophilia'],13351,,,,,C94355,,D010378,302.2,F65.4,,
mondo:0001693,ego-dystonic sexual orientation,,13352,,,,,,,,302.0,,,
mondo:0001694,diffuse interstitial keratitis,,13353,,,C0155089,,,,,370.52,,,
mondo:0001695,senile ectropion,['involutional ectropion'],13356,,,C0155193,,,,,374.11,,,
mondo:0001697,reading disorder,,13365,,,,,,,,315.09,,,
mondo:0001698,tinea profunda,"['deep seated dermatophytosis', 'Majocchi^s granuloma', 'granuloma trichophyticum']",13368,,,C1279621,,,,,,,,
mondo:0001699,tinea manuum,"['manus dermatophytosis', 'dermatophytosis of manus', 'Tinea manus', 'dermatophytosis of hand']",13369,,,C0153246,,,,,110.2,B35.2,,
mondo:0001700,megaloblastic anemia,"['megaloblastic anaemia (disease)', 'recessive hereditary megaloblastic anaemia 1', 'IGS', 'MGA1 Norwegian type', 'recessive hereditary megaloblastic anemia 1', 'Grasbeck-Imerslund syndrome', 'megaloblastic anemia', 'megaloblastic anemia (disease)', 'RH-MGA1']",13382,,,C0002888,,C34382,,,281.3,,,0001889
mondo:0001701,gastrointestinal anthrax,,13386,,,C0152945,,,,C571911,022.2,A22.2,,
mondo:0001702,labia majora carcinoma,"['labia majora carcinoma', 'labia majora cancer', 'carcinoma of labia majora', 'carcinoma of labium majora', 'carcinoma of the labia majora']",13389,,,C1334356,,C9363,,,,,,
mondo:0001703,color vision disorder,"['colour vision deficiency', 'color vision deficiency', 'color vision defects', 'blindness colour', 'color-vision disease', 'blindness color', 'colour blindness', 'color blindness', 'colour vision defects']",13399,,98658,CN207064,,C3891,,,368.59,,,
mondo:0001704,vaginal glandular neoplasm,"['vagina glandular cell neoplasm', 'vaginal glandular neoplasm', 'vaginal glandular tumour', 'vaginal glandular tumor']",134,,,C1519921,,C40250,,,,,,
mondo:0001705,pure red-cell aplasia,"['PRCA', 'primary red cell aplasia', 'red cell hypoplasia', 'pure red cell aplasia']",1340,,,C0034902,,C34974,,D012010,284.81,,,
mondo:0001706,cerebral sarcoidosis,"['sarcoidosis of telencephalon', 'cerebral sarcoidosis', 'telencephalon sarcoidosis']",13403,,,C0398676,,C35441,,,,,,
mondo:0001707,cardiac sarcoidosis,"['sarcoidosis of heart', 'heart sarcoidosis']",13405,,,C0392077,,C35589,,,,,,
mondo:0001708,pulmonary sarcoidosis,"['sarcoidosis of lung', 'lung sarcoidosis']",13406,,,C0036205,,C34997,,D017565,517.8,,,
mondo:0001709,hypercalcemic sarcoidosis,,13407,,,C1334067,,C35807,,,,,,
mondo:0001710,perforation of bile duct,,13409,,,C0156218,,,,,576.3,K83.2,,
mondo:0001711,hepatic encephalopathy,"['encephalopathy, hepatic', 'portal-systemic encephalopathy', 'Hepatoencephalopathy']",13413,,,C0019151,,C79596,,D006501,572.2,,,
mondo:0001712,alexia,"['Word Blindnesses, acquired', 'acquired Word Blindnesses', 'Blindnesses, acquired Word', 'Word blindness, acquired', 'dyslexia, acquired global', 'acquired Word blindness', 'aphemesthaesia', 'acquired spelling dyslexia', 'spelling dyslexia, acquired', 'acquired alexia', 'reading disability, acquired', 'acquired reading disability', 'disabilities, acquired reading', 'dyslexia, acquired spelling', 'acquired reading disabilities', 'disability, acquired reading', 'acquired dyslexia', 'alexia, acquired', 'reading disabilities, acquired', 'global dyslexia, acquired', 'blindness, acquired Word', 'acquired global dyslexia']",13417,,,,,,,D004411,315.01,,,
mondo:0001713,inherited aplastic anemia,"['constitutional aplastic anemia', 'rare constitutional aplastic anemia', 'congenital hypoplastic anemia', 'hypoplastic anaemia - familial', 'congenital aplastic anaemia', 'constitutional aplastic anaemia', 'congenital hypoplastic anaemia', 'rare constitutional aplastic anaemia', 'hereditary aplastic anaemia', 'hereditary aplastic anemia']",1342,,68383,C0949116,,,,D029502,284.09,D61.0,,
mondo:0001714,bejel,"['Dichuchwa', 'nonvenereal endemic syphilis', 'nonvenereal syphilis', 'Treponema pallidum subsp. endemicum caused disease or disorder', 'Njovera', 'endemic syphilis', 'Frenga']",13431,,,C0004945,,,,D014211,,,,
mondo:0001715,basilar artery occlusion,,13446,,,,,,,,433.01,,,
mondo:0001716,corneal argyrosis,"['argentous corneal deposits', 'argyrosis of cornea']",13447,,,C0155108,,,,,371.16,,,
mondo:0001717,posterior corneal pigmentation,['posterior corneal pigmentations'],13448,,,C0155106,,,,,371.13,,,
mondo:0001718,scleritis,"['scleritis', 'scleritis (disease)']",13452,,,C0036416,,C119046,,D015423,379.00,,,0100532
mondo:0001719,gonococcal bursitis,['Neisseria gonorrhoeae caused bursitis'],13453,,,C0153218,,,,,098.52,,,
mondo:0001720,gonococcal synovitis,"['gonococcal synovitis &/or tenosynovitis', 'gonococcal synovitis or tenosynovitis', 'gonococcal synovitis and tenosynovitis']",13454,,,C0343714,,,,,098.51,,,
mondo:0001721,urethral intrinsic sphincter deficiency,['intrinsic (urethral) sphincter deficiency [ISD]'],13461,,,C0375381,,,,,599.82,,,
mondo:0001722,central pterygium,,13473,,,C0155156,,,,,372.43,,,
mondo:0001723,progressive peripheral pterygium,,13474,,,C0155155,,,,,372.42,,,
mondo:0001724,supraglottis cancer,"['malignant tumour of supraglottis', 'malignant neoplasm of the supraglottis', 'malignant neoplasm of supraglottic part of larynx', 'malignant supraglottic neoplasm', 'malignant supraglottic tumor', 'malignant supraglottis tumor', 'malignant supraglottic tumour', 'malignant tumor of the supraglottis', 'Ca larynx - supraglottis', 'malignant tumor of supraglottis', 'malignant neoplasm of supraglottis', 'malignant tumour of the supraglottis', 'supraglottic part of larynx cancer', 'malignant supraglottis tumour', 'cancer of supraglottic part of larynx', 'malignant neoplasm of extrinsic larynx', 'malignant supraglottic part of larynx neoplasm', 'malignant supraglottis neoplasm']",13476,,,C0153484,,C3545,,,161.1,C32.1,,
mondo:0001725,balanitis xerotica obliterans,"['lichen Sclerosus of penis', 'penile lichen Sclerosus', 'lichen Sclerosus of the penis']",13477,,,C0152460,,C3523,,D052798,607.81,,,
mondo:0001727,active cochleovestibular Meniere disease,"['active Meniere^s disease, cochleovestibular', 'active cochleovestibular Meniere disease', 'cochleovestibular active Mnire^s disease', 'active cochleovestibular Meniere^s disease']",13490,,,C0155496,,,,,386.01,,,
mondo:0001728,active vestibular Meniere disease,"['vestibular active Mnire^s disease', 'active vestibular Meniere^s disease', 'active Meniere^s disease, vestibular', 'active vestibular Meniere disease']",13491,,,C0155498,,,,,386.03,,,
mondo:0001729,active cochlear Meniere disease,"['active cochlear Meniere disease', 'active cochlear Meniere^s disease', 'cochlear active Mnire^s disease', 'active Meniere^s disease, cochlear']",13492,,,C0155497,,,,,386.02,,,
mondo:0001730,urethral syndrome,,13498,,,C0156279,,,,,597.81,,,
mondo:0001731,benign vaginal mixed epithelial and mesenchymal neoplasm,"['benign vaginal carcinosarcoma', 'benign vaginal mixed epithelial and mesenchymal tumour', 'benign vaginal mixed epithelial and mesenchymal neoplasm', 'benign vaginal mixed epithelial and mesenchymal tumor']",135,,,C1511106,,C40275,,,,,,
mondo:0001732,trigonitis,['trigone of urinary bladder inflammation'],13507,,,C1261278,,C123175,,,595.3,N30.3,,
mondo:0001733,occlusion of tributary of retinal vein,"['venous tributary (branch) occlusion of retina', 'venous tributary occlusion of retina', 'venous tributary branch occlusion of retina']",13514,,,,,,,,362.36,,,
mondo:0001734,tuberous sclerosis,"['Bourneville^s disease', 'Phacomatosis, Bourneville', 'syndrome, Bourneville', 'tuberous sclerosis', 'sclerosis, tuberous', 'Epiloia', 'Bourneville-Pringles disease', 'tuberous sclerosis complex', 'tuberose sclerosis', 'sclerosis, tuberose', 'Bourneville phakomatosis', 'cerebral Scleroses', 'syndrome, Bourneville^s', 'phakomatosis, Bourneville', 'Bourneville syndrome', 'Bourneville pringle disease', 'Bourneville^s syndrome', 'cerebral sclerosis', 'Bourneville-pringle^s disease', 'sclerosis Tuberosa', 'Bourneville-pringle disease', 'disease, Bourneville-pringle^s', 'sclerosis, cerebral', 'tuberous sclerosis syndrome', 'TSC', 'disease, Bourneville-pringle', 'tuberous sclerosis Complex', 'Bourneville pringle^s disease', 'Bourneville Phacomatosis', 'Bourneville disease', 'adenoma sebaceum']",13515,,805,,"['-0.3223', '0.4536', '0.1731', '-0.513', '-0.0661', '-0.3127', '-0.10803', '0.536', '-0.7983', '-0.1577', '0.1808', '-0.0917', '-0.0511', '0.634', '-0.3535', '-0.537', '-0.4062', '-0.3916', '-0.4714', '0.1205', '-0.4507', '-0.2307', '0.001623', '-0.547', '0.5635', '-0.258', '0.0914', '0.4773', '0.673', '0.04932', '0.1132', '-1.004', '0.6177', '0.2488', '-0.3835', '0.555', '-0.7607', '-0.03668', '0.529', '-0.277', '0.7583', '-0.06113', '-0.0791', '-0.0946', '-0.3428', '0.001785', '0.07916', '-0.09033', '0.5522', '0.2615', '0.2336', '0.998', '-0.1274', '0.0754', '-0.1411', '-0.136', '-0.2615', '0.5273', '-0.0526', '-0.318', '-0.3958', '0.2001', '-0.01176', '0.247', '-0.2258', '0.5825', '0.4854', '0.999', '-0.9585', '0.4446', '0.1248', '-0.0842', '-0.1268', '-0.412', '0.02063', '0.2983', '0.007153', '0.6567', '0.06696', '-0.0346', '-0.2622', '0.1855', '-0.543', '-0.6694', '0.2355', '-0.5537', '0.169', '0.017', '0.2028', '0.739', '-0.1085', '0.798', '-0.1965', '0.05664', '0.3616', '0.10425', '-0.08356', '-0.0887', '0.1676', '0.2524']",C3424,,D014402,759.5,,10045138,
mondo:0001735,paranasal sinus disorder,"['paranasal sinus disease or disorder', 'disease of paranasal sinus', 'sinus disorder', 'disorder of paranasal sinus', 'paranasal sinus disorder', 'paranasal sinus disease', 'disorder of nasal sinus']",1352,,,C0030469,,C26843,,D010254,478.1,,,
mondo:0001736,neonatal infective mastitis,,13520,,,C0158948,,,,,771.5,P39.0,,
mondo:0001737,tetanus neonatorum,['neonatal tetanus'],13521,,,C0343312,,C116814,,,771.3,A33,,
mondo:0001739,purulent labyrinthitis,"['suppurative labyrinthitis', 'acute suppurative labyrinthitis', 'bacterial labyrinthitis']",13534,,,C0155506,,,,,386.33,,,
mondo:0001740,cornea squamous cell carcinoma,"['epidermoid carcinoma of cornea', 'squamous cell carcinoma of the cornea', 'epidermoid carcinoma of the cornea', 'cornea squamous cell carcinoma', 'corneal epidermoid carcinoma', 'cornea epidermoid carcinoma', 'squamous cell carcinoma of cornea', 'corneal squamous cell carcinoma']",13538,,,C0346366,,C4552,,,,,,
mondo:0001741,hyperparathyroidism,['hyperparathyroidism'],13543,,,C0020502,,C48259,0008506,D006961,252.00,,,
mondo:0001742,interval angle-closure glaucoma,"['angle-closure glaucoma, subacute', 'intermittent angle-closure glaucoma', 'prodromal angle closure glaucoma']",13549,,,C0154945,,,,,365.21,,,
mondo:0001743,paranasal sinus lymphoma,"['lymphoma of paranasal sinus', 'lymphoma of the paranasal sinus', 'lymphoma of accessory sinus', 'lymphoma of the accessory sinus', 'accessory sinus lymphoma', 'primary paranasal sinus lymphoma', 'paranasal sinus lymphoma']",1355,,,C1335339,,C6068,,,,,,
mondo:0001744,angle-closure glaucoma,"['primary open-angle glaucoma with narrow angles', 'ACG - angle-closure glaucoma', 'angle closure glaucoma', 'Narrow cleft glaucoma']",13550,,,C0017605,,,,D015812,,,,
mondo:0001745,subserous uterine fibroid,['subserous leiomyoma of uterus'],13560,,,C0153995,,,,,218.2,,,
mondo:0001746,optic disk drusen,"['optic nerve head drusen', 'drusen of optic disc', 'drusen of optic disk']",13561,,,C0029128,,,,D015594,377.21,,,
mondo:0001747,tibial collateral ligament bursitis,,13566,,,C0158315,,,,,726.62,,,
mondo:0001748,maxillary sinus carcinoma,"['malignant neoplasm of maxillary sinus', 'malignant neoplasm of the maxillary sinus', 'maxillary sinus cancer', 'malignant maxillary sinus tumour', 'malignant neoplasm of antrum', 'malignant tumor of the maxillary sinus', 'malignant maxillary sinus tumor', 'cancer of maxillary sinus', 'malignant tumour of the maxillary sinus', 'carcinoma of maxillary sinus', 'malignant tumour of maxillary sinus', 'malignant maxillary sinus neoplasm', 'malignant tumor of maxillary sinus', 'maxillary sinus carcinoma']",1357,,,,,C9332,,,160.2,,,
mondo:0001749,cortical senile cataract,"['senile cataract of lens cortex', 'cortical senile cataract', 'lens cortex senile cataract']",13574,,,C0154980,,,,,366.15,,,
mondo:0001750,non-renal secondary hyperparathyroidism,,13575,,,,,,,,252.02,,,
mondo:0001751,cholestasis,"['obstruction of bile duct', 'bile occlusion']",13580,,,C0008370,,,,D002779,576.2,,,
mondo:0001752,alveolar periostitis,"['dry tooth socket', 'dry socket', 'extrinsic allergic alveolitis of jaw skeleton', 'alveolitis of jaw', 'jaw skeleton extrinsic allergic alveolitis']",13585,,,C0013240,,,,D004368,526.5,,,
mondo:0001753,female infertility of uterine origin,"['infertility, female, of uterine origin']",13589,,,,,,,,628.3,N97.2,,
mondo:0001754,eclampsia,"['eclampsia in puerperium', 'eclampsia, postpartum', 'postpartum eclampsia']",13593,,,C0156678,,C87167,,D004461,642.64,O15,,
mondo:0001756,frontal sinus cancer,"['malignant frontal sinus tumor', 'cancer of frontal sinus', 'malignant neoplasm of frontal sinus', 'malignant tumor of frontal sinus', 'malignant tumor of the frontal sinus', 'malignant tumour of the frontal sinus', 'malignant frontal sinus neoplasm', 'malignant frontal sinus tumour', 'frontal sinus cancer', 'malignant tumour of frontal sinus', 'malignant neoplasm of the frontal sinus']",1360,,,C0153478,,C3542,,,160.4,C31.2,,
mondo:0001757,frontal sinus neoplasm,"['tumor of the frontal sinus', 'frontal sinus neoplasm (disease)', 'neoplasm of frontal sinus', 'frontal sinus tumour', 'frontal sinus tumor', 'tumour of the frontal sinus', 'neoplasm of the frontal sinus', 'tumor of frontal sinus', 'tumour of frontal sinus']",1361,,,C0345672,,C4419,,,,,,
mondo:0001758,paranasal sinus sarcoma,"['paranasal sinus sarcoma', 'sarcoma of paranasal sinus', 'sarcoma of the accessory sinus', 'sarcoma of accessory sinus', 'accessory sinus sarcoma', 'sarcoma of the paranasal sinus']",1362,,,C1335342,,C6849,,,,,,
mondo:0001760,photokeratitis,['ultraviolet keratitis'],13626,,,C0155078,,C118750,,,370.24,,,
mondo:0001761,favism,,13628,,,C0015702,,C34607,,D005236,,,,
mondo:0001762,dentine erosion,"['tooth erosion, non-bacterial of dentine', 'dentine tooth erosion, non-bacterial']",13629,,,,,,,,521.32,,,
mondo:0001763,ethmoid sinus cancer,"['malignant tumour of the ethmoid sinus', 'malignant ethmoidal sinus neoplasm', 'malignant tumor of the ethmoid sinus', 'malignant ethmoid sinus neoplasm', 'malignant neoplasm of ethmoidal sinus', 'malignant neoplasm of the ethmoid sinus', 'malignant ethmoidal sinus tumour', 'malignant neoplasm of the ethmoidal sinus', 'malignant tumor of the ethmoidal sinus', 'ethmoid sinus cancer', 'malignant ethmoidal sinus tumor', 'malignant tumour of ethmoid sinus', 'malignant tumour of the ethmoidal sinus', 'malignant neoplasm of ethmoid sinus', 'malignant tumor of ethmoid sinus', 'malignant tumour of ethmoidal sinus', 'cancer of ethmoid sinus', 'malignant ethmoid sinus tumor', 'malignant ethmoid sinus tumour', 'malignant tumor of ethmoidal sinus']",1363,,,C0153477,,C3541,,,160.3,C31.1,,
mondo:0001764,ethmoidal sinus neoplasm,"['tumor of the ethmoid sinus', 'tumour of the ethmoidal sinus', 'neoplasm of ethmoidal sinus', 'tumour of the ethmoid sinus', 'ethmoid sinus tumor', 'tumour of ethmoid sinus', 'ethmoidal sinus neoplasm', 'tumor of ethmoidal sinus', 'neoplasm of ethmoid sinus', 'neoplasm of the ethmoidal sinus', 'tumour of ethmoidal sinus', 'neoplasm of the ethmoid sinus', 'tumor of the ethmoidal sinus', 'ethmoidal sinus tumor', 'ethmoidal sinus tumour', 'tumor of ethmoid sinus', 'ethmoid sinus neoplasm', 'ethmoid sinus tumour', 'ethmoid sinus neoplasm (disease)']",1364,,,C0345668,,C4416,,,,,,
mondo:0001765,polyneuropathy in collagen vascular disease,,13649,,,C0154759,,,,,357.4,,,
mondo:0001766,eversion of lacrimal punctum,,13651,,,C0155243,,,,,375.51,,,
mondo:0001767,stenosis of lacrimal punctum,,13653,,,C0155244,,,,,375.52,,,
mondo:0001768,stenosis of lacrimal passage,['stenosis of lacrimal canaliculi'],13654,,,,,,,,375.53,,,
mondo:0001769,acquired tear duct stenosis,"['stenosis of nasolacrimal duct, acquired', 'acquired nasolacrimal duct stenosis', 'acquired stenosis of nasolacrimal duct', 'tear duct - acquired stenosis']",13655,,,,,,,,375.56,,,
mondo:0001770,gastrin secretion abnormality,,13656,,,C0000774,,,,,251.5,,,
mondo:0001771,infective urethral stricture,,13658,,,,,,,,598.01,,,
mondo:0001772,ulcer of anus and rectum,['anal and rectal ulcer'],13662,,,,,,,,569.41,K62.6,,
mondo:0001773,post-vaccinal encephalitis,"['encephalitis following immunisation procedures', 'encephalitis following immunization procedures', 'postvaccinal encephalomyelitis']",13664,,,C0751101,,,,D004673,323.51,,,
mondo:0001774,posterior scleritis,,13676,,,C0155357,,,,,379.07,,,
mondo:0001775,chronic duodenal ileus,,13687,,,C0156087,,,,,537.2,,,
mondo:0001776,prostate calculus,"['Stone of prostate', 'calculus of prostate', 'prostatic lithiasis', 'prostatic stone', 'prostate gland lower urinary tract calculus', 'lower urinary tract calculus of prostate gland']",13689,,,C0149525,,,,,602.0,N42.0,,
mondo:0001777,acute gonococcal cystitis,"['acute gonorrhea of bladder', 'gonococcal cystitis, acute', 'acute gonorrhoea of bladder', 'gonococcal cystitis (acute)']",13690,,,C0153191,,,,,098.11,,,
mondo:0001778,dermoid cyst of skin,"['skin dermoid', 'cutaneous dermoid cyst', 'dermoid cyst of skin', 'cystic skin teratoma', 'subcutaneous dermoid cyst', 'dermoid cyst of the skin', 'skin dermoid cyst', 'zone of skin dermoid cyst', 'dermoid cyst of skin (finding)']",13691,,,C0349502,,C4632,,,,,,
mondo:0001779,vaginal squamous papilloma,"['vaginal squamous papilloma', 'vagina squamous papilloma', 'squamous papilloma of vagina', 'squamous papilloma of the vagina']",137,,,C1336943,,C6374,,,,,,
mondo:0001780,premature ejaculation,"['premature ejaculation', 'premature ejaculation (disease)']",13709,,,,,C94349,,D061686,302.75,F52.4,,0012876
mondo:0001781,uterine corpus adenomatoid tumor,"['uterine corpus localized epithelial mesothelioma', 'body of uterus adenomatoid tumour', 'body of uterus adenomatoid tumor', 'uterine corpus adenomatoid tumor', 'uterine corpus localised epithelial mesothelioma']",1371,,,C1336902,,C27250,,,,,,
mondo:0001782,mature cataract,"['total or mature cataract', 'total, mature senile cataract']",13717,,,,,,,,366.17,,,
mondo:0001783,endometrial stromal nodule,,1373,,,C0334485,,C4262,1000241,,,,,
mondo:0001784,malignant renovascular hypertension,,13730,,,,,,,,,,,
mondo:0001785,malignant secondary hypertension,,13731,,,C0155617,,,,,405.09,,,
mondo:0001786,uterine inflammatory disease,['inflammatory disease of the uterus'],13736,,,C0269047,,,,,615.9,,,
mondo:0001787,hepatic infarction,['infarct of liver'],13738,,,C0151731,,,,D000081011,573.4,,,
mondo:0001788,nutmeg liver,['chronic passive congestion of liver'],13739,,,C0156195,,,,,573.0,,,
mondo:0001789,neurofibroma of spinal cord,"['spinal cord neurofibroma', 'neurofibroma of spinal cord']",13742,,,C1336047,,C5145,,,,,,
mondo:0001790,spinal cord lipoma,"['lipoma of spinal cord', 'spinal cord lipoma']",13743,,645276,C0347446,,C4619,,,214.8,,,
mondo:0001791,neonatal urinary tract infectious disease,['urinary tract infection of newborn'],1375,,,C0235815,,,,,771.82,,,
mondo:0001792,epiphora due to insufficient drainage,,13756,,,C0155234,,,,,375.22,,,
mondo:0001793,excessive tearing,"['apparatus disease, lacrimal', 'watering eye', 'excessive tear production', 'disease, lacrimal apparatus', 'apparatus diseases, lacrimal', 'lacrimal apparatus disease', 'epiphora', 'diseases, lacrimal apparatus']",13757,,,C0152227,,,,D007766,375.20,,,
mondo:0001794,Pthirus pubis infestation,"['pediculosis pubis', 'Phthirus/pediculus pubis - pubic lice - crabs', 'Pediculus pubis', 'Phthirus/pediculus pubis - pubic lice - crabs (& infestation)', 'phthiriasis pubis', 'Pthirus pubis infection', 'phthiriasis', 'infestation by Phthirus pubis', 'crabs', 'Phthirus pubis', 'infections, Pthirus pubis', 'Phthirus pubis [pubic louse]']",13760,,,C0030759,,C35777,,,132.2,B85.3,,
mondo:0001795,plantar wart,"['verruca plantaris', 'plantar wart']",13775,,,C0042548,,C26913,1002023,,078.12,B07.0,,
mondo:0001797,chancroid,"['Chancroids', 'Ulcus molle, skin']",13778,,,C0007947,,,,D002602,099.0,A57,,
mondo:0001798,hypermobility syndrome,['benign joint hypermobility'],13781,,,C0152093,,,,,728.5,M35.7,,
mondo:0001799,localized anterior staphyloma,"['anterior staphyloma, localised', 'anterior staphyloma, localized']",13787,,,C0155362,,,,,379.14,,,
mondo:0001800,equatorial staphyloma,,13788,,,C0155361,,,,,379.13,,,
mondo:0001801,staphyloma posticum,,13789,,,C0155360,,,,,379.12,,,
mondo:0001802,acute tympanitis,['acute myringitis'],13790,,,C0155460,,,,,384.00,,,
mondo:0001803,myringitis bullosa hemorrhagica,['bullous myringitis'],13791,,,C0155461,,,,,384.01,,,
mondo:0001804,anterior scleritis,,13794,,,C0155353,,,,,379.03,,,
mondo:0001805,female breast central part cancer,"['malignant neoplasm of central part of female breast', 'malignant neoplasm of central portion of female breast']",13799,,,C0153549,,,,,174.1,,,
mondo:0001806,vaginal squamous tumor,"['vagina squamous cell neoplasm', 'vaginal squamous tumor', 'vaginal squamous neoplasm']",138,,,C1519931,,C40242,,,,,,
mondo:0001808,chronic subinvolution of uterus,,13811,,,C0156370,,,,,621.1,,,
mondo:0001809,adhesions of uterus,"['intrauterine synechiae', 'band of uterus']",13812,,,CN199257,,,,,621.5,,,
mondo:0001810,hypoglossal nerve disorder,"['disorder of 12th nerve', 'disease of hypoglossal nerve', 'disorder of XII nerve', 'twelfth nerve disorder', 'disorder of the XII nerve', 'hypoglossal nerve disorder', 'disorder of hypoglossal nerve', 'disorder of hypoglossal [12th] nerve', 'hypoglossal nerve disease', 'hypoglossal nerve disease or disorder']",13814,,,C0152181,,C26954,,D020437,352.5,,,
mondo:0001811,tetanic cataract,['hypocalcaemic cataract'],13822,,,C0039613,,C35068,,,366.42,,,
mondo:0001812,parasitic eyelid infestation,['parasitic infestation of eyelid'],13823,,,C0155183,,,,,373.6,,,
mondo:0001813,squamous blepharitis,,13825,,,C0155174,,,,,373.02,,,
mondo:0001815,extrapyramidal and movement disease,,13839,,,C0477355,,,,,333.90,G20-G26,,
mondo:0001816,scleroperikeratitis,['scleritis with corneal involvement'],13861,,,C0155355,,,,,379.05,,,
mondo:0001817,acute closed-angle glaucoma,"['acute angle-closure glaucoma', 'angle-closure glaucoma, acute']",13862,,,C0154946,,,,,365.22,,,
mondo:0001818,facial neuralgia,"['neuralgia of facial nerve', 'facial nerve neuralgia']",13865,,,,,,,D005156,351.8,,,
mondo:0001819,multiple cranial nerve palsy,['multiple cranial nerve palsies'],13866,,,C0154733,,,,,352.6,,,
mondo:0001820,focal labyrinthitis,['circumscribed labyrinthitis'],13867,,,C0155505,,,,,386.32,,,
mondo:0001821,hypoactive sexual desire disorder,['lack or loss of sexual desire'],13868,,,,,C94337,,,302.71,F52.0,,
mondo:0001822,hypolipoproteinemia,"['hypolipoproteinemia (disease)', 'hypolipoproteinemia', 'hypolipoproteinaemia', 'lipoprotein deficiencies']",1387,,,,,,,D007009,272.5,,,0010981
mondo:0001823,sick sinus syndrome,"['SSS', 'sinus node infection']",13884,,,,,C62244,,D012804,,I49.5,,
mondo:0001824,polyneuropathy,['polyneuropathy'],1389,,,C0152025,,C26951,,D011115,357.4,,,
mondo:0001825,squamous papilloma,"['papilloma, squamous cell, benign', 'squamous cell papilloma (morphologic abnormality)', 'epidermoid papilloma', 'squamous cell papilloma', 'squamous papilloma', 'epidermoid cell papilloma', 'keratotic papilloma']",139,,,C0205874,,C3712,1001970,,,,,
mondo:0001827,white piedra,['Tinea blanca'],13902,,,C0040249,,,,,111.2,B36.2,,
mondo:0001828,acquired color blindness,"['acquired color vision deficiencies', 'acquired color vision deficiency', 'acquired colour vision disorder', 'acquired colour vision deficiency', 'acquired color vision disorder', 'acquired colour vision deficiencies']",13912,,,,,C118712,,,368.55,H53.52,,
mondo:0001829,lumbosacral plexus lesion,"['lumbosacral nerve plexus nerve plexus disease', 'nerve plexus disease of lumbosacral nerve plexus', 'lumbosacral plexus lesions']",13913,,,C0154735,,,,,353.1,,,
mondo:0001830,somatization disorder,"['Briquet^s disorder', 'Somatisation disorder', 'Polysomatising disorder']",13918,,,,,,,,300.81,F45.0,,
mondo:0001831,irregular astigmatism,,13919,,,C0152194,,,,,367.22,,,
mondo:0001832,bacterial esophagitis,['bacterial esophagitis'],13921,,,C0341108,,C27106,,,,,,
mondo:0001833,lacrimal duct obstruction,"['obstruction of lacrimal canaliculus', 'blocked lacrimal canaliculus', 'obstruction of lacrimal ducts']",13929,,,,,,,D007767,,,,
mondo:0001834,visual pathway disorder,"['disease of optic tract', 'optic tract disease or disorder', 'disorder of optic tract', 'optic tract disease', 'visual pathway disorder']",1393,,,C0155287,,C35342,,,,H47.9,,
mondo:0001835,facial paralysis,"['palsy of face', 'facial palsy', 'face palsy']",13934,,,C0015469,,,,D005158,,,,
mondo:0001836,amenorrhea,"['amenorrhea (disease)', 'amenorrhea', 'amenia', 'absence of menstruation']",13938,,,C0002453,,C61443,,D000568,626.0,,,0000141
mondo:0001837,acute gonococcal salpingitis,"['gonococcal salpingitis, specified as acute', 'gonococcal salpingitis, acute']",13942,,,C0275654,,,,,098.17,,,
mondo:0001838,acute gonococcal prostatitis,"['gonococcal prostatitis (acute)', 'gonococcal prostatitis', 'acute gonococcal prostatitis', 'gonococcal prostatitis, acute']",13943,,,C0153192,,,,,098.12,,,
mondo:0001841,uterine corpus epithelioid leiomyoma,,13951,,,C1519850,,C40164,,,,,,
mondo:0001842,uterine corpus dissecting leiomyoma,"['Cotyledonoid dissecting leiomyoma', 'Sternberg tumor', 'Sternberg tumour']",13953,,,C1519847,,C40172,,,,,,
mondo:0001843,uterus interstitial leiomyoma,['intramural leiomyoma of uterus'],13955,,,C0153994,,,,,218.1,D25.1,,
mondo:0001844,uterine corpus myxoid leiomyoma,,13956,,,C1519860,,C40166,,,,,,
mondo:0001845,uterine corpus lipoleiomyoma,['uterine corpus lipomatous leiomyoma'],13957,,,C1519856,,C40168,1000614,,,,,
mondo:0001846,uterine corpus bizarre leiomyoma,"['bizarre leiomyoma of body of uterus', 'body of uterus bizarre leiomyoma', 'uterine corpus bizarre leiomyoma', 'uterine corpus Symplastic leiomyoma', 'uterine corpus leiomyoma, atypical variant', 'uterine corpus leiomyoma with bizarre nuclei']",13958,,,C1519853,,C40167,,,,,,
mondo:0001847,nuclear senile cataract,"['Senile nuclear cataract', 'Senile nuclear sclerosis', 'lens nucleus senile cataract', 'senile cataract of lens nucleus']",13963,,,,,,,,366.16,,,
mondo:0001848,Morgagni cataract,['hypermature cataract'],13964,,,C0152258,,,,,366.18,,,
mondo:0001849,chronic orbital inflammation,['chronic inflammation of orbit'],1397,,,C0155261,,,,,376.10,,,
mondo:0001850,female breast lower-outer quadrant cancer,['malignant neoplasm of lower-outer quadrant of female breast'],13972,,,C0153553,,,,,174.5,,,
mondo:0001851,primary lacrimal atrophy,,1399,,,C0155229,,,,,375.13,,,
mondo:0001852,small intestine lymphoma,"['small intestinal lymphoma', 'primary small intestinal lymphoma', 'lymphoma of the small bowel', 'lymphoma of the small intestine', 'lymphoma of small bowel', 'small bowel lymphoma', 'lymphoma of small intestine', 'small intestine lymphoma']",13996,,,C0278805,,C4007,,,202.80,,,
mondo:0001853,contact blepharoconjunctivitis,,13999,,,C0155150,,,,,372.22,,,
mondo:0001854,lacrimal apparatus disorder,"['lacrimal apparatus disease or disorder', 'lacrimal system disorder', 'lacrimal system disease', 'disorder of lacrimal system', 'disease of lacrimal apparatus', 'disorder of lacrimal apparatus', 'lacrimal apparatus disease']",1400,,,,,C26809,,D007766,375.9,,,
mondo:0001855,rubeosis iridis,,14000,,,C0154916,,,,,364.42,,,
mondo:0001856,splenic artery aneurysm,,14006,,,C0155747,,,,,442.83,,,
mondo:0001857,Brucella canis brucellosis,,14019,,,C0494040,,,,,023.3,,,
mondo:0001858,Tietze syndrome,"['Tietze syndrome', 'syndromic disease of costochondral joint', 'costochondral joint syndromic disease', 'Costochondritis', 'Tietze^s syndrome', 'Chondropathia tuberosa', 'Costalchondritis', 'costochondral junction syndrome', 'Tietze^s disease', 'slipping rib syndrome']",14021,,,C0040213,,C168333,,D013991,733.6,,,
mondo:0001859,algoneurodystrophy,,14022,,,,,,,,733.7,M89.0,,
mondo:0001860,folic acid deficiency anemia,"['folate-deficient megaloblastic anemia', 'folate-deficient megaloblastic anaemia', 'folate deficiency anemia', 'folate deficiency anaemia', 'folate-deficiency anemia', 'folate-deficiency anaemia']",14026,,,C0151482,,,,,281.2,,,
mondo:0001861,malignant parietal pleura tumor,['primary malignant neoplasm of parietal pleura'],14032,,,C0153495,,,,,,,,
mondo:0001862,malignant visceral pleura tumor,['primary malignant neoplasm of visceral pleura'],14033,,,C0153496,,,,,,,,
mondo:0001863,aorta atresia,"['atresia and stenosis of aorta', 'congenital atresia and stenosis of aorta']",14037,,,,,,,,747.22,Q25.2,,
mondo:0001864,residual stage angle-closure glaucoma,['residual stage of angle-closure glaucoma'],1404,,,C0154948,,,,,365.24,,,
mondo:0001866,bipolar I disorder,,14042,,,,,,,,296.7,,,
mondo:0001867,phaeohyphomycosis,"['infection by dematiacious fungi [Phaehyphomycosis]', 'infection by dematiacious fungi', 'phaehyphomycosis']",14049,,,,,,,D060446,117.8,,,
mondo:0001868,primary angle-closure glaucoma,['primary angle closure glaucoma'],1405,,,C0017606,,C34640,1001506,,365.20,H40.2,,
mondo:0001869,paraurethral gland cancer,"['malignant tumor of the paraurethral gland', 'cancer of paraurethral gland', 'malignant neoplasm of paraurethral gland', 'malignant tumor of paraurethral gland', 'paraurethral gland cancer', 'malignant tumour of the paraurethral gland', 'malignant tumour of paraurethral gland', 'malignant paraurethral gland neoplasm']",14059,,,C0153621,,,,,189.4,,,
mondo:0001870,acute poststreptococcal glomerulonephritis,['post-streptococcal glomerulonephritis'],14064,,,C0403414,,C35443,,,,,,
mondo:0001871,acute diffuse glomerulonephritis,"['acute diffuse glomerulonephritis', 'diffuse glomerulonephritis, acute', 'acute diffuse nephritis']",14066,,,C0341689,,C35587,,,,,,
mondo:0001873,geniculate ganglionitis,"['geniculate ganglion inflammation', 'geniculate ganglionitis']",14075,,,C0017407,,,,,351.1,G51.1,,
mondo:0001874,toxic labyrinthitis,,14081,,,C0155507,,,0006951,,386.34,,,
mondo:0001875,epicondylitis,"['andrel epicondylitis', 'lateral epicondylitis', 'shooter^s elbow', 'ectepicondyle of humerus inflammation', 'archer^s elbow', 'medial epicondylitis', 'hockey elbow', 'tennis elbow', 'golfer^s elbow']",14087,,,C0014488,,C34589,,D013716,726.32,M77.1,,
mondo:0001876,renal artery atheroma,"['atherosclerosis of renal artery', 'renal atherosclerosis', 'renal artery atherosclerosis']",14092,,,C0155734,,,,,440.1,I70.1,,
mondo:0001877,infertility due to extratesticular cause,['infertility due to extratesticular causes'],14096,,,C0021360,,,,,606.8,,,
mondo:0001878,acquired hypertrophic pyloric stenosis,"['adult hypertrophic pyloric stenosis', 'acquired gastric outlet stenosis', 'acquired hypertrophic pyloric stenosis']",14099,,,C2937286,,,,,537.0,,,
mondo:0001879,anus cancer,"['malignant anus neoplasm', 'malignant tumor of the anus', 'malignant anal neoplasm', 'malignant anal tumour', 'malignant tumor of anus', 'malignant anal tumor', 'anus cancer', 'malignant neoplasm of the anus', 'malignant tumour of the anus', 'cancer of anus', 'malignant neoplasm of anus', 'malignant tumour of anus']",14110,,,C0153445,,C7379,,,154.3,,,
mondo:0001880,median rhomboid glossitis,['persistent tuberculum impar'],14111,,,,,,,,750.19,K14.2,,
mondo:0001881,toxic shock syndrome,"['syndrome (TSS), toxic shock', 'toxic shock syndrome, (TSS)', 'bacterial toxic-shock syndrome', 'TSS', 'shock syndrome (TSS), toxic', 'bacterial TSS', 'toxic shock syndrome', 'TSS, toxic shock syndrome', 'staphylococcal toxic shock syndrome', 'toxic shock']",14115,,36234,CN204669,,C35498,,D012772,040.82,A48.3,,
mondo:0001882,bacteriuria,"['bacteriuria (disease)', 'bacteriuria']",1412,,,C0004659,,,,D001437,,,10004056,0012461
mondo:0001883,blue toe syndrome,,14121,,,C0242645,,,,D018438,,,,
mondo:0001884,abducens nerve neoplasm,"['tumor of abducens nerve', 'tumour of sixth cranial nerve', 'sixth cranial nerve tumor', 'VIth cranial nerve tumours', 'neoplasm of the sixth cranial nerve', 'tumor of the abducens nerve', 'sixth cranial nerve neoplasms', 'tumour of the sixth cranial nerve', 'tumor of sixth cranial nerve', 'neoplasm of abducens nerve', 'sixth cranial nerve tumour', 'sixth cranial nerve tumours', 'tumour of abducens nerve', 'abducens nerve neoplasm (disease)', 'abducens nerve tumors', 'VIth cranial nerve neoplasms', 'VIth cranial nerve tumors', 'tumour of the abducens nerve', 'tumor of the sixth cranial nerve', 'sixth cranial nerve neoplasm', 'sixth cranial nerve tumors', 'abducens nerve tumour', 'neoplasm of sixth cranial nerve', 'abducens nerve tumours', 'neoplasm of the abducens nerve', 'abducens nerve neoplasms', 'abducens nerve tumor']",14125,,,C1263898,,C5826,,,239.7,,,
mondo:0001885,lateral cystocele,,14130,,,C2711750,,,,,618.02,N81.12,,
mondo:0001886,midline cystocele,,14131,,,C1456248,,,,,618.01,N81.11,,
mondo:0001887,Allen-Masters syndrome,"['Masters-Allen syndrome', 'Broad ligament laceration syndrome']",14133,,,C0152079,,,,,620.6,,,
mondo:0001888,anus lymphoma,"['lymphoma of the anus', 'primary anal lymphoma', 'anus lymphoma', 'lymphoma of anus', 'anal lymphoma']",14139,,,C1332268,,C5601,,,,,,
mondo:0001889,ovarian dysfunction,"['ovarian failure', 'ovarian insufficiency', 'ovarian hypofunction']",1414,,,,,C113351,0009003,,256.9,E28,,
mondo:0001890,pulp erosion,"['dental pulp tooth erosion, non-bacterial', 'tooth erosion, non-bacterial of dental pulp']",14140,,,,,,,,521.33,,,
mondo:0001892,spinal cord lymphoma,"['lymphoma of the spinal cord', 'lymphoma of spinal cord', 'spinal cord cancer', 'spinal cord lymphoma', 'primary spinal cord lymphoma']",14150,,,C1336044,,C5157,,,,,,
mondo:0001893,spinal cord melanoma,"['spinal cord melanoma', 'spinal cord melanoma (disease)', 'melanoma of the spinal cord', 'melanoma of spinal cord']",14151,,,C1336045,,C5158,,,,,,
mondo:0001894,spinal cord sarcoma,"['spinal cord sarcoma', 'sarcoma of spinal cord', 'sarcoma of the spinal cord']",14152,,,C1336049,,C5152,,,,,,
mondo:0001895,acute retrobulbar neuritis,"['retrobulbar neuritis, acute', 'retrobulbar neuritis (acute)']",14155,,,C0155301,,,,,377.32,,,
mondo:0001896,obstructive hydrocephalus,['non-communicating hydrocephalus'],14159,,,C0549423,,C116347,,,331.4,G91.1,,
mondo:0001897,bilateral hyperactive labyrinth,"['hyperactive bilateral labyrinthine dysfunction', 'hyperactive labyrinth, bilateral']",14165,,,C0155516,,,,,386.52,,,
mondo:0001898,optic choroid disorder,"['optic choroid disease or disorder', 'optic choroid disease', 'choroid disease', 'disease of optic choroid', 'choroid disorder', 'disorder of optic choroid']",1417,,,C0008521,,C34468,,D015862,363.9,,,
mondo:0001899,rheumatic congestive heart failure,"['rheumatic heart failure', 'congestive rheumatic heart failure', 'rheumatic heart failure (congestive)']",14172,,,C0155582,,,,,398.91,I09.81,,
mondo:0001901,selective IgG subclass deficiency,"['selective immunoglobulin G deficiency', 'selective IgG deficiency disease', 'selective Immunoglobulin G subclass deficiency', 'Immunoglobin G subclass deficiency', 'selective IgG immunodeficiency', 'selective deficiency of IgG']",14176,,,,,C27024,,D017099,279.03,,,
mondo:0001902,congenital agammaglobulinemia,"['congenital hypogammaglobulinaemia', 'congenital agammaglobulinemia', 'congenital hypogammaglobulinemia (finding)']",14177,,,C1457897,,,,,279.04,,,
mondo:0001903,calcific tendinitis,,14181,,,C0521515,,,,,726.11,M65.2,,
mondo:0001904,polyneuropathy due to drug,,14184,,,C0154762,,,,,357.6,,,
mondo:0001905,bicipital tenosynovitis,,14192,,,C0158304,,,,,726.12,,,
mondo:0001906,posterior dislocation of lens,,14199,,,C0155373,,,,,379.34,,,
mondo:0001907,adult dermatomyositis,"['dermatomyositis of adults', 'adult onset dermatomyositis']",14202,,,,,C27313,,,,,,
mondo:0001909,renal tubular acidosis,,14219,,,C0001126,,,,D000141,588.89,,,
mondo:0001910,ochronosis disorder,['ochronosis'],14223,,,C0028817,,C84938,,D009794,270.2,,,0030764
mondo:0001911,tracheal calcification,['calcification of trachea'],14224,,,C0264324,,,,,519.19,,,0002787
mondo:0001912,acute frontal sinusitis,"['frontal sinusitis, acute']",14225,,,C0155805,,,,,461.1,J01.1,,
mondo:0001913,oligospermia,,14228,,,C0028960,,,,D009845,606.1,,,0000798
mondo:0001914,scleromalacia perforans,,14230,,,C0155354,,,,,379.04,,,
mondo:0001915,orbital cyst,,14233,,,C0155285,,,,,376.81,,,0001144
mondo:0001916,gastrointestinal tularemia,"['enteric tularemia', 'intestinal tularaemia']",14239,,,,,,,,021.8,A21.3,,
mondo:0001917,chronic perichondritis of pinna,"['perichondritis of auricle, chronic', 'chronic pinna perichondritis', 'chronic perichondritis of auricle']",14243,,,C0155391,,,,,380.02,,,
mondo:0001918,epiphora due to excess lacrimation,,14244,,,C0155233,,,,,375.21,,,
mondo:0001919,cystoid macular retinal degeneration,['cystoid macular degeneration of retina'],14245,,,C0154850,,,,,362.53,,,
mondo:0001920,chronic purulent otitis media,"['suppurative otitis media, chronic', 'chronic suppurative otitis media', 'CSOM', 'chronic suppurative otitis Media']",14247,,,C0271454,,C128386,,,382.3,,,
mondo:0001921,chronic atticoantral disease,['chronic atticoantral suppurative otitis media'],14248,,,C0565831,,,,,382.2,,,
mondo:0001922,pyoureter,['ureter abscess'],1425,,,C0034223,,C35666,,,593.89,,,
mondo:0001923,vitreoretinal dystrophy,['vitreoretinal dystrophies'],14251,,,C0154863,,,,,362.73,H35.51,,
mondo:0001924,dystrophies primarily involving the retinal pigment epithelium,,14252,,,,,,,,362.76,H35.54,,
mondo:0001925,retinal dystrophy in systemic or cerebroretinal lipidoses,,14253,,,,,,,,362.71,,,
mondo:0001926,ureteral disorder,"['ureter disease or disorder', 'ureter disorder', 'ureteric disorder', 'ureteric disease', 'disease of ureter', 'disorder of ureter', 'ureter disease']",1426,,,C0403608,,C27148,,D014515,,,,
mondo:0001927,pulmonary valve insufficiency,"['pulmonary regurgitation', 'pulmonary regurg.', 'pulmonic insufficiency', 'pulmonic valve regurgitation', 'pulmonary incompetence', 'pulmonary valve regurgitation', 'regurgitation, pulmonary', 'pulmonary valvular regurgitation', 'pulmonary incompetence, non-rheumatic', 'pulmonary insufficiency following trauma and surgery']",14265,,,,,C50848,,D011665,,,,
mondo:0001928,suppurative cholangitis,['suppurative cholangitis'],14269,,,C0267924,,C35336,,,,,,
mondo:0001929,ascending cholangitis,['ascending cholangitis'],14270,,,C0311273,,C35372,,,,,,
mondo:0001930,acute cholangitis,"['cholangitis, acute', 'acute cholangitis']",14271,,,C0267917,,C35334,,,,,,
mondo:0001931,pericholangitis,,14272,,,C0031052,,C34916,,,,,,
mondo:0001933,endocrine pancreas disorder,"['endocrine pancreas disease', 'disease of endocrine pancreas', 'disorder of endocrine pancreas', 'endocrine pancreas disorder', 'endocrine pancreas disease or disorder']",1428,,,C0271633,,C27067,,,251,,,
mondo:0001935,neurogenic arthropathy,"['Charcot^s joint', 'neuropathic arthropathy (& Charcot^s)', 'arthropathy associated with neurological disorder', 'Charcot^s arthropathy', 'neuropathic arthropathy']",14286,,,C0003892,,,1001378,D001177,713.5,,,
mondo:0001936,brawny scleritis,,14287,,,C0155356,,,,,379.06,,,
mondo:0001938,vulvar dystrophy,['dystrophy of vulva'],14292,,,C0013426,,C34565,,,624.09,,,
mondo:0001939,skin epithelioid hemangioma,"['histiocytoid hemangioma of the skin', 'skin epithelioid hemangioma', 'epithelioid hemangioma of skin', 'epithelioid hemangioma of the skin', 'angiolymphoid hyperplasia of the skin', 'zone of skin histiocytoid hemangioma', 'histiocytoid hemangioma of zone of skin', 'angiolymphoid hyperplasia of skin', 'angiolymphoid cutaneous hyperplasia', 'histiocytoid hemangioma of skin']",14308,,,C0002989,,C7393,1001424,D000796,,,,
mondo:0001940,pleuropneumonia,,14319,,,C0032241,,,,D011001,,,,
mondo:0001941,blindness (disorder),"['vision loss', 'vision impairment', 'visual impairment', 'blindness']",1432,,,,,C97109,,D001766,369,H54,,
mondo:0001942,generalized anxiety disorder,['GAD'],14320,,,,,C92622,1001892,,300.02,F41.1,,
mondo:0001943,Plasmodium malariae malaria,"['quartan malaria', 'malaria by Plasmodium malariae']",14324,,,C0024536,,C34799,,,084.2,B52,,
mondo:0001944,mixed malaria,"['malaria by more than one parasite', 'malaria fever by more than one parasite']",14325,,,C0153121,,,,,084.5,,,
mondo:0001945,postencephalitic Parkinson disease,"['postencephalitic Parkinsonism', 'postencephalitic parkinsonism']",14332,,97349,C0030568,,C34898,1001402,D010301,,,,
mondo:0001947,suppurative thyroiditis,"['suppurative thyroiditis', 'acute suppurative thyroiditis', 'infectious thyroiditis', 'abscess of thyroid']",14350,,,C0040150,,C129724,1001431,D013969,,E06.0,,
mondo:0001949,acute thyroiditis,"['thyroiditis (disease), acute']",14353,,,C0001360,,,,,245.0,E06.0,,
mondo:0001950,corneal ectasia,,1436,,,C0155135,,,,,371.71,,,
mondo:0001951,Norwegian scabies,"['seven year itch', 'crusted scabies']",14374,,,C0028425,,C34855,,,,,,
mondo:0001952,parietal lobe cancer,"['parietal lobe neoplasm', 'cancer of parietal lobe', 'parietal lobe cancer', 'malignant neoplasm of parietal lobe', 'tumour of parietal lobe', 'malignant parietal lobe neoplasm']",14384,,,C0153637,,,,,191.3,C71.3,,
mondo:0001953,pyuria,"['pus cells in urine', 'pyuria', 'pyuria (disease)']",1439,,,,,,,D011776,,,,0012085
mondo:0001954,thrombophlebitis migrans,,14392,,,C0152250,,,,,453.1,I82.1,,
mondo:0001955,protozoal dysentery,,14397,,,,,,,,007.8,,,
mondo:0001956,capillary leak syndrome,"['Clarkson disease', 'AVLS', 'idiopathic capillary leak syndrome', 'systemic capillary leak syndrome', 'capillary hyperpermeability syndrome', 'capillary leak syndrome with monoclonal gammopathy', 'CLS', 'capillary leak syndrome', 'SCLS', 'acute vascular leak syndrome', 'periodic systemic capillary leak syndrome']",14400,,188,C0343084,,C62578,,D019559,448.9,,10007196,
mondo:0001957,critical illness polyneuropathy,,14402,,,C0393851,,,,D011115,357.82,G62.81,,
mondo:0001959,labyrinthine bilateral reactive loss,"['loss of labyrinthine reactivity, bilateral', 'bilateral loss of labyrinthine reactivity']",14413,,,C0155520,,,,,386.56,,,
mondo:0001962,abnormality of glucagon secretion,['glucagon secretion abnormality'],14427,,,C0154191,,,,,251.4,,,
mondo:0001964,chronic tubotympanic suppurative otitis media,,14435,,,C0155440,,,,,382.1,H66.1,,
mondo:0001965,sclerosing keratitis,['sclerokeratitis'],14444,,,C0155090,,,,,370.54,,,
mondo:0001966,chronic closed-angle glaucoma,"['chronic narrow angle glaucoma', 'angle-closure glaucoma, chronic', 'chronic angle-closure glaucoma', 'anatomical narrow angle glaucoma']",14445,,,C0154947,,,,,365.23,,,
mondo:0001967,gonadal dysgenesis,['gonadal dysgenesis syndrome'],14447,,,,"['-0.02806', '0.02492', '-0.000914', '-0.01714', '0.0367', '-0.04395', '-0.002369', '0.07104', '-0.04855', '-0.04697', '-0.01231', '-0.03818', '-0.02922', '0.012215', '-0.0409', '-0.06027', '0.010506', '-0.01532', '-0.0006313', '-0.1366', '-0.003273', '-0.02495', '0.058', '-0.04', '0.02562', '0.00247', '0.00248', '0.00589', '0.02084', '-0.05948', '0.08154', '0.003239', '0.07526', '0.02176', '-0.00768', '-0.0471', '0.02203', '-0.02562', '-0.0143', '-0.05322', '0.0648', '-0.034', '0.0348', '-0.0101', '0.007107', '-0.02608', '-0.003088', '0.02173', '0.01467', '0.04678', '0.00823', '-0.03023', '0.0175', '0.009865', '-0.04343', '0.010796', '0.0717', '-0.05896', '-0.073', '0.001363', '0.04437', '0.02383', '0.00339', '0.02602', '-0.01223', '0.01559', '0.0653', '0.06088', '-0.06073', '0.06165', '-0.0541', '0.04202', '0.0235', '-0.04315', '0.001673', '0.01248', '0.02745', '0.00406', '-0.06046', '-0.03513', '-0.0196', '0.03903', '-0.007225', '0.05502', '-0.03232', '-0.01543', '0.01686', '0.03183', '0.05063', '0.009834', '0.01566', '0.06415', '-0.03796', '-0.007153', '0.1271', '-0.02295', '0.065', '-0.05026', '-0.01401', '0.01415']",C61420,,D006059,758.6,,,
mondo:0001969,mixed gonadal dysgenesis,['gonadal dysgenesis mixed'],14449,,,C0018055,,,,D006060,,,,
mondo:0001971,farmer^s lung disease,"['Farmers lung', 'farmer lung', 'farmer^s lung']",14453,,99906,C0015634,,C34605,,,495.0,,10016221,
mondo:0001972,Brucella melitensis brucellosis,,14456,,,C0302362,,,,,023.0,,,
mondo:0001973,Brucella abortus brucellosis,,14457,,,,,,,D002007,023.1,,,
mondo:0001974,hemangioma of orbit,"['hemangioma of the orbit', 'orbit angioma', 'angioma of the orbit', 'angioma of orbit', 'orbit hemangioma']",14459,,,C1335128,,C6245,,,228.09,,,
mondo:0001975,cavernous hemangioma of orbit,"['cavernous angioma of the orbit', 'orbit cavernous angioma', 'cavernous angioma of orbit', 'cavernous hemangioma of the orbit', 'orbit cavernous hemangioma']",14463,,,C0346352,,C4546,,,228.09,,,
mondo:0001976,chorea gravidarum,,14483,,,C0264746,,,1001290,D020150,646.80,,,
mondo:0001977,ureteral lymphoma,"['lymphoma of ureter', 'lymphoma of the ureter', 'ureter lymphoma', 'primary ureter lymphoma', 'ureteral lymphoma']",14489,,,C1336876,,C6175,,,,,,
mondo:0001978,regional ureteric cancer,"['regional malignant ureteral tumor', 'regional ureter carcinoma', 'regional malignant ureteral tumour', 'regional ureteric carcinoma']",14491,,,C0854921,,C9356,,,,,,
mondo:0001979,dumping syndrome,"['dumping (jejunal) syndrome', 'jejunal syndrome']",14495,,,C0013288,,C2994,1001307,D004377,,,,
mondo:0001982,Niemann-Pick disease,"['sphingomyelin/cholesterol lipidosis', 'lipoid histiocytosis', 'lipoid histiocytosis (classical phosphatide)', 'type A Niemann-Pick disease', 'sphingomyelinase deficiency disease', 'sphingomyelin lipidosis', 'Niemann-Pick disease, subacute juvenile form', 'Niemann-Pick disease with cholesterol esterification block']",14504,,,C0028064,,C61269,1001380,D009542,,,,
mondo:0001983,peripheral degeneration of cornea,['peripheral degenerations of cornea'],14507,,,C0155123,,,,,371.48,,,
mondo:0001984,candidal paronychia,"['candidiasis of skin and nails', 'candidiasis of skin']",14512,,,C1282977,,,,,112.3,,,
mondo:0001985,partial arterial retinal occlusion,"['retinal partial arterial occlusion', 'partial retinal arterial occlusion']",14522,,,C0154839,,C35192,,,362.33,,,
mondo:0001986,Argyll Robertson pupil,"['Argyll Robertson pupil, atypical', 'atypical Argyll-Robertson pupil', 'Argyll Robertson phenomenon or pupil, nonsyphilitic']",14523,,,C0155375,,,,,379.45,H57.01,,
mondo:0001987,senile degeneration of brain,['Senile brain degen.'],14524,,,C0154669,,,,,331.2,,,
mondo:0001988,external pathological resorption,,14529,,,C0266878,,,,,521.42,,,
mondo:0001989,atrophic glossitis,"['smooth atrophic tongue', 'atrophy of tongue papillae', 'glossitis, Hunter^s', 'Hunter^s glossitis']",1453,,,C0155964,,,,,529.4,K14.4,,
mondo:0001990,malignant cardiac peripheral nerve sheath neoplasm,"['malignant heart peripheral nerve sheath tumour', 'MPNST of heart', 'Cardiac malignant peripheral nerve sheath tumor', 'malignant heart peripheral nerve sheath neoplasm', 'CARDIAC schwannoma, malignant', 'Cardiac malignant peripheral nerve sheath tumour', 'malignant schwannoma of the heart', 'heart malignant peripheral nerve sheath tumour', 'malignant heart peripheral nerve sheath tumor', 'malignant peripheral nerve sheath tumor of heart', 'malignant peripheral nerve sheath tumour of the heart', 'heart MPNST', 'malignant heart schwannoma', 'malignant Cardiac neurilemmoma', 'malignant schwannoma of heart', 'malignant neurilemmoma of the heart', 'malignant Cardiac peripheral nerve sheath tumour', 'heart malignant peripheral nerve sheath tumor', 'malignant peripheral nerve sheath neoplasm of the heart', 'malignant Cardiac peripheral nerve sheath neoplasm', 'malignant heart neurilemmoma', 'malignant Cardiac schwannoma', 'malignant peripheral nerve sheath tumor of the heart', 'MPNST of the heart', 'malignant Cardiac peripheral nerve sheath tumor', 'malignant peripheral nerve sheath neoplasm of heart', 'malignant neurilemmoma of heart', 'malignant peripheral nerve sheath tumour of heart', 'Cardiac MPNST']",14534,,,C1334569,,C5367,,,,,,
mondo:0001991,malignant cardiac germ cell tumor,"['malignant germ cell tumor of the heart', 'malignant Cardiac germ cell tumour', 'malignant Cardiac germ cell neoplasm', 'malignant Cardiac germ cell tumor', 'malignant heart germ cell tumor', 'malignant heart germ cell tumour', 'malignant germ cell neoplasm of the heart', 'malignant germ cell tumour of the heart', 'malignant heart germ cell neoplasm', 'malignant germ cell neoplasm of heart', 'malignant germ cell tumour of heart', 'malignant germ cell tumor of heart']",14535,,,C1334566,,C5371,,,,,,
mondo:0001992,rete testis adenocarcinoma,"['adenocarcinoma of the rete testis', 'rete testis adenocarcinoma', 'adenocarcinoma of rete testis', 'carcinoma, rete testis, malignant']",14544,,,C0863024,,C8955,,,,,,
mondo:0001993,seminal vesicle adenocarcinoma,['seminal vesicle adenocarcinoma'],14545,,,C1519233,,C39906,,,,,,
mondo:0001994,sphenoidal sinus cancer,"['malignant sphenoid sinus neoplasm', 'malignant neoplasm of the sphenoid sinus', 'malignant tumor of the sphenoidal sinus', 'malignant neoplasm of sphenoidal sinus', 'malignant tumour of the sphenoidal sinus', 'malignant tumour of sphenoidal sinus', 'malignant sphenoid sinus tumor', 'malignant neoplasm of the sphenoidal sinus', 'malignant tumor of the sphenoid sinus', 'cancer of sphenoidal sinus', 'malignant tumour of the sphenoid sinus', 'malignant neoplasm of sphenoid sinus', 'malignant tumor of sphenoid sinus', 'malignant tumour of sphenoid sinus', 'malignant sphenoidal sinus neoplasm', 'sphenoidal sinus cancer', 'malignant sphenoidal sinus tumour', 'malignant sphenoid sinus tumour', 'malignant sphenoidal sinus tumor', 'malignant tumor of sphenoidal sinus']",14546,,,C0153479,,C3543,,,160.5,C31.3,,
mondo:0001995,sphenoid sinus squamous cell carcinoma,"['epidermoid carcinoma of sphenoid sinus', 'squamous cell carcinoma of the sphenoid sinus', 'squamous cell carcinoma of the sphenoidal sinus', 'sphenoid sinus epidermoid carcinoma', 'sphenoidal sinus squamous cell carcinoma', 'epidermoid carcinoma of the sphenoidal sinus', 'squamous cell carcinoma of sphenoidal sinus', 'sphenoidal sinus epidermoid carcinoma', 'sphenoid sinus squamous cell carcinoma', 'squamous cell carcinoma of sphenoid sinus', 'epidermoid carcinoma of sphenoidal sinus', 'epidermoid carcinoma of the sphenoid sinus']",14547,,,C1336039,,C6066,,,,,,
mondo:0001996,steroid-induced glaucoma - borderline,"['steroid responders borderline glaucoma', 'borderline glaucoma steroid responder']",14548,,,C0339572,,,,,365.03,,,
mondo:0001997,root resorption,,14550,,,C0035851,,,,D012391,,,,
mondo:0001998,Foster-Kennedy syndrome,,14555,,,C0152112,,,1001330,,377.04,,,
mondo:0001999,primary pulmonary hypertension,"['pulmonary hypertension, primary']",14557,,,,,,,,416.0,I27.0,,
mondo:0002000,anaerobic meningitis,['meningitis caused by anaerobic bacteria'],14559,,,C0854214,,,,,320.81,,,
mondo:0002002,postsurgical hypothyroidism,"['post-surgical hypothyroidism', 'postoperative hypothyroidism']",1458,,,C0154157,,,,,244.0,,,
mondo:0002003,papilledema,"['papilloedema', 'Choked disk', 'edema of the optic disk', 'oedema of the optic disc', 'Choked disc']",146,,,,,C3307,,D010211,377.31,,,
mondo:0002004,atheroembolism of kidney,"['cholesterol embolism of kidney', 'kidney cholesterol embolism']",1460,,,,,,,,,I75.81,,
mondo:0002006,serous labyrinthitis,['acute serous labyrinthitis'],1467,,,C0155504,,,,,386.31,,,
mondo:0002008,labyrinthitis,"['inner ear infection', 'internal ear inflammation', 'otitis interna']",3930,,,C0022893,,C128369,,D007762,386.30,H83.0,,
mondo:0002009,major depressive disorder,"['major depressive disorder, response to citalopram therapy in', 'major depressive disorder', 'unipolar depression', 'unipolar depression, susceptibility to', 'single major depressive episode', 'major depression', 'major depressive disorder 1', 'major depressive disorder 2', 'recurrent major depression', 'major depressive disorder and accelerated response to antidepressant drug treatment']",2848,608516,,,,C35094,0003761,D003865,296.30,,,
mondo:0002010,FG syndrome,"['intellectual disability, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum', 'Keller syndrome', 'FGS', 'Opitz-Kaveggia syndrome', 'mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum', 'FGS1']",14711,,323,,,,,,759.89,,,
mondo:0002012,methylmalonic acidemia,"['METHYLMALONICACIDURIA due to methylmalonic CoA mutase deficiency', 'methylmalonic acidemia, cblB type', 'methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA type', 'methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB type', 'methylmalonic aciduria type cblA', 'methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency', 'methylmalonic acidemia, cblA type', 'methylmalonic aciduria cblB type', 'methylmalonic aciduria type cblB', 'METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl B', 'methylmalonic aciduria, mut type', 'METHYLMALONICACIDURIA, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin--Cbl A', 'methylmalonic aciduria mut type', 'methylmalonic aciduria']",14749,,,C1855119,,C98986,,C537358,270.7,E71.120,,
mondo:0002013,lymphangioma,"['congenital lymphangioma', 'benign lymphangioma (morphologic abnormality)', 'benign lymphangioma', 'LM', 'lymphangioma, benign', 'lymphangioma']",1475,,2415,CN201700,,C8965,,D008202,228.1,,,
mondo:0002014,"autosomal recessive Ehlers-Danlos syndrome, vascular type","['Ehlers-Danlos syndrome, vascular type, autosomal recessive', 'Ehlers-Danlos syndrome, recessive type 4']",14759,,,C0268340,,,,,,,,
mondo:0002016,benign familial neonatal epilepsy,['familial neonatal seizures'],14777,,,,,,,,,,,
mondo:0002017,olivopontocerebellar atrophy,"['OPCA', 'WADIA-swami syndrome', 'Dejerine-Thomas syndrome', 'Thomas^ syndrome']",14784,,,C0028968,,C84947,,D009849,333.0,,,
mondo:0002021,gingival disorder,"['gingiva disease', 'gingiva disease or disorder', 'disorder of gingiva', 'disease of gingiva']",1483,,,C0017563,,C173795,,D005882,,,,
mondo:0002022,disorder of orbital region,"['disorder of orbital region', 'orbital region disease or disorder', 'eye and adnexa disease', 'disease of orbital region', 'orbital region disease']",1492,,,,,,,,362.10,H00-H59,,
mondo:0002025,psychiatric disorder,"['Psychiatric disorder', 'disease of mental health', 'mental disorder', 'mental illness', 'mental dysfunction', 'Psychiatric disease']",150,,,,,C2893,,D001523,,,,
mondo:0002026,candidiasis,"['infections, Candida <Debaryomycetaceae>', 'Candidosis', 'systemic candidiasis', 'Candida <Debaryomycetaceae> infection', 'Candida infection', 'disseminated candidiasis', 'thrush']",1508,,,C0006840,,C26711,,D002177,112.9,B37,,
mondo:0002027,avoidant personality disorder,['anxious personality disorder'],1509,,,,,C92636,,,301.82,F60.6,,
mondo:0002028,personality disorder,"['character disorder', 'personality disorder (disease)', 'personality disorder']",1510,,,,,C34922,,,301.9,,,0012075
mondo:0002029,chronic gonorrhea of cervix,"['gonococcal cervicitis, chronic', 'chronic gonococcal cervicitis']",1512,,,C0153206,,,,,098.35,,,
mondo:0002030,chronic cervicitis,"['cervicitis (disease), chronic']",1513,,,C0269062,,C27057,,,,,,
mondo:0002031,cecal disorder,"['disease of caecum', 'caecum disease', 'caecum disease or disorder', 'disorder of caecum']",1518,,,C0007527,,,,D002429,,,,
mondo:0002032,colon carcinoma,"['carcinoma of colon', 'colon carcinoma', 'carcinoma of the colon', 'colon cancer', 'colonic carcinoma']",1520,,,C0699790,,C4910,1001950,,,,,
mondo:0002033,cecum cancer,"['malignant neoplasm of the cecum', 'cancer of caecum', 'malignant cecum tumour', 'malignant tumour of the cecum', 'malignant neoplasm of caecum', 'malignant tumor of the cecum', 'caecum cancer', 'malignant caecum neoplasm', 'malignant cecum tumor', 'malignant tumor of cecum', 'malignant neoplasm of cecum', 'malignant cecum neoplasm', 'malignant tumour of cecum']",1521,,,C0153437,,C9329,,,153.4,,,
mondo:0002034,cecum lymphoma,"['primary cecum lymphoma', 'lymphoma of the cecum', 'lymphoma of cecum', 'lymphoma of caecum', 'caecum lymphoma', 'cecum lymphoma', 'cecal lymphoma']",1522,,,C1332867,,C5515,,,,,,
mondo:0002035,colon lymphoma,"['primary colon lymphoma', 'colon lymphoma', 'colonic lymphoma', 'lymphoma of colon', 'lymphoma of the colon']",1523,,,C0519037,,C4793,,,202.80,,,
mondo:0002036,penile disorder,"['penile disease', 'penile disorder', 'penis disease', 'disorder of penis', 'disease of penis', 'penis disease or disorder']",1529,,,C0030846,,C26846,,D010409,607.9,,,
mondo:0002037,pleural disorder,"['pleura disease or disorder', 'disorder of pleura', 'pleural disorders', 'non-neoplastic pleural disease', 'pleural disorder', 'disease of pleura', 'pleura disease']",1532,,,C0032226,,C26859,,D010995,518.89,,,
mondo:0002038,head and neck carcinoma,"['carcinoma of craniocervical region', 'carcinoma of the neck', 'craniocervical region carcinoma', 'head and neck carcinoma', 'neck carcinoma', 'carcinoma of head and neck', 'head and neck cancer', 'carcinoma of neck', 'carcinoma of the head and neck']",1542,,,C3887461,,C35850,,,,,,
mondo:0002039,cognitive disorder,"['cognitive disease', 'organic mental disorder', 'cognitive disorder']",1561,,,,,C92196,1001457,D019965,294.9,,,
mondo:0002040,dermatomycosis,,1563,,,C0011630,,,,D003881,111.9,,,
mondo:0002041,fungal infectious disease,"['mycoses', 'fungal infection', 'mycosis', 'infection, fungal', 'Fungi infection', 'Fungi caused disease or disorder', 'infections, Fungi']",1564,,,,,C3245,,D009181,117.9,B35-B49,,
mondo:0002042,mechanical ectropion,,1569,,,C0155194,,,,,374.12,,,
mondo:0002043,ectropion,"['ectropion of eyelid', 'ectropion', 'everted margin', 'ectropion (disease)']",1570,,,C0013592,,,,D004483,374.10,,,0000656
mondo:0002044,spastic ectropion,,1571,,,C0155195,,,,,374.13,,,
mondo:0002045,communicating hydrocephalus,['non-obstructive hydrocephalus'],1573,,,C0009451,,C34501,,,331.3,G91.0,,
mondo:0002046,alcohol abuse,"['addiction, alcohol', 'alcohol use disorder', 'intoxication, chronic alcoholic', 'alcohol dependence', 'abuse, alcohol', 'ethanol abuse', 'alcoholism', 'alcohol addiction', 'chronic alcoholic intoxication', 'alcoholic intoxication, chronic', 'alcohol abuse', 'dependence, alcohol']",1574,,,,,,,D000437,305.00,,,
mondo:0002047,pulmonary systemic sclerosis,"['lung disease with systemic sclerosis', 'lung involvement in systemic sclerosis', 'scleroderma lung disease']",1578,,,C0339904,,,,,517.2,,,
mondo:0002048,thrombocytopenia due to immune destruction,"['thrombocytopenia due to platelet alloimmunization', 'thrombocytopenia due to immune destruction', 'auto-immune thrombocytopenia', 'immune thrombocytopenia']",1587,,,,,C3991,,,,,,
mondo:0002049,thrombocytopenia,"['thrombocytopenic disorder', 'platelet count decreased']",1588,,,CN130080,,C3408,,D013921,287.5,,,
mondo:0002050,depressive disorder,"['mental depression', 'syndromes, depressive', 'depression', 'syndrome, depressive', 'melancholias', 'melancholia']",1596,,,CN236658,,C2982,,D003866,311,F32,,
mondo:0002051,integumentary system disorder,"['disorder of integumental system', 'disease of integumental system', 'integumentary disease', 'integumental system disease or disorder', 'integumental system disease']",16,,,C1290011,,,,,,,,
mondo:0002052,lymphadenitis,"['adenitis', 'lymph gland infection', 'chronic lymphadenitis', 'acute adenitis', 'acute lymphadenitis', 'chronic adenitis', 'lymphadenitis (disease)', 'lymphadenitis', 'lymph node inflammation', 'Inflammation of lymph node', 'lymph nodeitis']",1602,,,C0157705,,C26821,,D008199,683,,,0002840
mondo:0002055,benign eccrine breast spiradenoma,"['benign breast eccrine spiradenoma', 'benign eccrine breast spiradenoma', 'benign eccrine spiradenoma of breast', 'benign eccrine spiradenoma of the breast']",1616,,,C1332492,,C5193,,,,,,
mondo:0002056,breast fibroadenoma,"['breast fibroadenoma', 'fibroadenoma of breast', 'fibroadenoma of the breast', 'Complex fibroadenoma of breast', 'fibroadenoma, benign', 'juvenile fibroadenoma of breast', 'FA', 'juvenile fibroadenoma', 'fibroadenoma', 'juvenile fibroadenoma (morphologic abnormality)', 'cellular fibroadenoma']",1618,,,C0346158,,C3744,1000254,D018226,,,,
mondo:0002057,breast leiomyoma,"['breast leiomyoma', 'leiomyoma of breast']",1623,,,C1511317,,C40399,,,,,,
mondo:0002058,breast adenoma,"['Ademoma - breast', 'breast adenoma']",1625,,,C1328385,,C40382,,,,,,
mondo:0002060,intraductal papilloma,"['intraductal papilloma', 'duct adenoma', 'intraductal papilloma (morphologic abnormality)', 'duct papilloma', 'ductal papilloma']",1627,,,C0206713,,C3785,,D018300,,,,
mondo:0002061,intraductal papillary breast neoplasm,['intraductal papillary breast neoplasm'],1628,,,C1334252,,C36090,,,,,,
mondo:0002062,breast myofibroblastoma,['breast myofibroblastoma'],1629,,,C1511320,,C40397,,,,,,
mondo:0002063,breast papillomatosis,"['papillomatosis of the breast', 'papillomatosis of breast', 'breast papillomatosis']",1634,,,C1332636,,C6977,,,,,,
mondo:0002064,breast angiomatosis,,1637,,,C1511284,,C40381,,,,,,
mondo:0002065,benign breast adenomyoepithelioma,"['breast adenomyoepithelioma, benign', 'benign adenomyoepithelioma of breast', 'benign breast adenomyoepithelioma', 'benign adenomyoepithelioma of the breast']",1641,,,C1332477,,C5144,,,,,,
mondo:0002066,breast adenomyoepithelioma,"['breast adenomyoepithelioma with malignant change', 'malignant adenomyoepithelioma of breast', 'BRAME', 'adenomyoepithelioma of the breast', 'breast adenomyoepithelioma']",1642,,,C1510795,,C6899,,,,,,
mondo:0002067,female breast upper-inner quadrant cancer,['malignant neoplasm of upper-inner quadrant of female breast'],1647,,,C0153550,,,,,174.2,C50.2,,
mondo:0002068,female breast lower-inner quadrant cancer,['malignant neoplasm of lower-inner quadrant of female breast'],1649,,,C0153551,,,,,174.3,C50.3,,
mondo:0002069,female breast axillary tail cancer,"['malignant neoplasm of axillary tail of breast', 'malignant axillary tail of breast neoplasm', 'cancer of axillary tail of breast']",1650,,,C0153554,,,,,174.6,C50.6,,
mondo:0002070,ventricular septal defect,"['ventricular septal defect', 'ventricular septal defects', 'VSD', 'ventricular septal defect (disease)', 'heart septal defects, ventricular', 'interventricular communication', 'ventricular septal abnormality', 'interventricular septal defect']",1657,,1480,,"['-0.2184', '-0.1142', '0.2537', '-0.09845', '0.3965', '-0.2302', '0.2659', '0.424', '-0.2708', '-0.04755', '-0.2467', '-0.67', '-0.0877', '0.2288', '-0.1015', '-0.3538', '-0.4673', '-0.3748', '-0.3535', '-0.3271', '0.1244', '0.1873', '0.4421', '-0.0781', '0.2598', '-0.4595', '0.3264', '0.226', '0.0935', '0.11755', '0.3237', '0.05624', '0.2092', '0.1997', '-0.00552', '-0.001871', '0.331', '0.1561', '0.1313', '-0.522', '0.2339', '-0.0757', '-0.0697', '0.1547', '0.003054', '-0.1127', '0.1293', '0.3362', '-0.1876', '0.1404', '-0.03986', '-0.03607', '0.02663', '0.03674', '-0.3516', '-0.2197', '0.05084', '0.2347', '-0.503', '-0.1023', '-0.2302', '0.2493', '0.06445', '0.385', '-0.2448', '0.01743', '0.518', '0.1359', '-0.3127', '-0.2334', '-0.1815', '0.1868', '0.1555', '0.03796', '-0.0215', '0.067', '0.2842', '-0.2393', '-0.3972', '-0.2382', '-0.1631', '-0.04144', '0.1298', '0.04684', '0.1274', '-0.26', '0.3406', '0.2373', '-0.01817', '-0.05927', '-0.1711', '0.02983', '0.3674', '0.11005', '0.669', '-0.1687', '0.33', '-0.1907', '-0.4258', '0.03162']",C84506,,D006345,745.4,,,0001629
mondo:0002071,supratentorial cancer,"['brain neoplasm, supratentorial', 'supratentorial neoplasms, malignant', 'malignant supratentorial tumour', 'malignant supratentorial tumor', 'malignant supratentorial neoplasm']",1659,,,,,C4964,,D015173,,,,
mondo:0002072,melanotic neuroectodermal tumor,"['pigmented neuroectodermal tumour', 'melanotic neuroectodermal tumor (morphologic abnormality)', 'melanotic Progonoma', 'melanotic neuroectodermal tumour of infancy', 'pigmented neuroectodermal tumour of infancy', 'melanotic neuroectodermal tumour of infancy (morphologic abnormality)', 'infantile melanotic neuroectodermal neoplasm', 'melanotic neuroectodermal tumour (morphologic abnormality)', 'MNTI', 'retinal anlage neoplasm', 'melanotic neuroectodermal tumor of infancy', 'pigmented neuroectodermal tumor of infancy', 'pigmented neuroectodermal tumor', 'melanotic neuroectodermal tumor of infancy (morphologic abnormality)']",166,,,C0206094,,C3717,1001038,D017600,,,,
mondo:0002073,malignant pineal area germ cell neoplasm,"['pineal cell tumor', 'malignant germ cell tumor of pineal parenchyma', 'malignant pineal gland germ cell tumour', 'pineal region germinoma', 'malignant germ cell tumor of pineal gland', 'malignant germ cell tumour of the pineal gland', 'malignant germ cell neoplasm of the pineal parenchyma', 'malignant germ cell tumour of the pineal parenchyma', 'malignant pineal area germ cell tumour', 'pineal cell tumour', 'malignant germ cell neoplasm of pineal parenchyma', 'malignant pineal parenchymal germ cell neoplasm', 'malignant germ cell tumour of pineal gland', 'malignant germ cell tumour of pineal parenchyma', 'malignant germ cell neoplasm of the pineal gland', 'malignant pineal parenchymal germ cell tumor', 'pineal germ cell neoplasm, malignant', 'pineal germ cell tumour', 'malignant pineal gland germ cell neoplasm', 'malignant pineal gland germ cell tumor', 'malignant pineal region germ cell tumour', 'pineal germ cell tumor', 'malignant pineal parenchymal germ cell tumour', 'malignant pineal region germ cell tumor', 'malignant germ cell tumor of the pineal gland', 'malignant germ cell tumor of the pineal parenchyma', 'malignant pineal region germ cell neoplasm', 'malignant pineal area germ cell tumor', 'malignant germ cell neoplasm of pineal gland', 'pineal region germ cell tumor', 'pineal region germ cell tumour']",1660,,,C1334612,,C6767,,,239.7,,,
mondo:0002074,Behcet syndrome arthropathy,"['arthropathy in Behcet^s syndrome', 'arthropathy in Behcet^s syndrome involving shoulder region', 'Behcet^s syndrome arthropathy', 'arthropathy in Behcet^s syndrome involving ankle and foot', 'arthropathy in Behcet^s syndrome involving hand', 'arthropathy in Behcet^s syndrome involving forearm', 'arthropathy in Behcet^s syndrome involving upper arm', 'arthropathy in Behcet^s syndrome involving pelvic region and thigh', 'Behcet syndrome arthropathy', 'arthropathy in Behcet^s syndrome involving lower leg', 'arthropathy in Behcet^s syndrome involving multiple sites']",1670,,,C0157770,,C35225,,,711.28,,,
mondo:0002075,spontaneous tension pneumothorax,,1672,,,C0155907,,,,,512.0,J93.0,,
mondo:0002076,pneumothorax,"['pneumothorax (disease)', 'pneumothorax']",1673,,,,,C38006,,D011030,512.8,,,0002107
mondo:0002077,low implantation of placenta,,1677,,,,,,,,641.0,,,
mondo:0002078,heart septal defect,"['septal defect', 'congenital septal defect', 'Cardiac septal defects', 'holes in the heart', 'congenital septal defect of heart']",1681,,,C0018816,,C84482,,D006343,745.9,,,
mondo:0002081,musculoskeletal system disorder,"['musculoskeletal system disorder', 'disorder of musculoskeletal system', 'musculoskeletal disease', 'musculoskeletal system disease', 'disease of musculoskeletal system', 'musculoskeletal system disease or disorder']",17,,,C0026857,,C107377,,D009140,729.99,,,
mondo:0002082,endocrine gland neoplasm,"['endocrine system neoplasm', 'endocrine system tumor', 'endocrine gland neoplasm (disease)', 'endocrine gland tumour', 'endocrine tumour', 'tumor of endocrine gland', 'tumour of endocrine gland', 'endocrine system tumour', 'endocrine neoplasm', 'endocrine gland tumor', 'neoplasm of endocrine gland', 'endocrine tumor', 'malignant endocrine tumour', 'malignant endocrine tumor']",,,,,,C3010,0003769,,239.7,,,
mondo:0002083,Richter syndrome,"['Richter^s syndrome', 'Richter^s transformation', 'Richter transformation', 'Richter syndrome']",1703,,,C0349631,,C35424,,,,,,
mondo:0002085,benign shuddering attacks,,1713,,,C0375200,,,,,333.93,G25.83,,
mondo:0002086,clear cell acanthoma,"['clear cell acanthoma (morphologic abnormality)', 'Degos acanthoma', 'pale (clear cell) acanthoma']",172,,,C0333992,,C97041,,,,,,
mondo:0002087,peritoneum cancer,"['cancer of peritoneum', 'peritoneal cancer', 'peritoneum cancer', 'malignant peritoneum neoplasm', 'peritoneal cavity cancer', 'malignant neoplasm of peritoneum', 'malignant peritoneal neoplasm', 'peritoneal neoplasm', 'cancer of the peritoneum']",1725,,,C0153467,,C3538,,,159.8,,,
mondo:0002088,partial retinal vein occlusion,"['partial retinal vein occlusion', 'partial occlusion of retinal vein']",1726,,,C0271080,,C35341,,,,,,
mondo:0002089,retinal vascular occlusion,"['retinal vascular occlusion', 'retinal vascular occlusion, unspecified']",1729,,,C0035326,,C34980,,,362.30,H34,,
mondo:0002090,eccrine sweat gland neoplasm,"['eccrine tumor', 'eccrine tumor of the skin', 'eccrine neoplasm of the skin', 'eccrine sweat gland tumor', 'tumor of eccrine sweat gland', 'eccrine skin tumour', 'eccrine sweat gland tumour', 'eccrine tumour', 'eccrine tumour of the skin', 'eccrine skin tumor', 'eccrine neoplasm of skin', 'eccrine neoplasm', 'neoplasm of eccrine sweat gland', 'eccrine tumor of skin', 'tumour of eccrine sweat gland', 'eccrine tumour of skin', 'eccrine sweat gland neoplasm (disease)', 'eccrine skin neoplasm']",173,,,C1333371,,C6796,,,,,,
mondo:0002092,small intestine leiomyoma,"['small intestinal leiomyoma', 'leiomyoma, small bowel', 'leiomyoma, small intestine', 'leiomyoma of small bowel', 'leiomyoma of small intestine', 'leiomyoma of the small intestine', 'small intestine leiomyoma', 'leiomyoma of the small bowel', 'small bowel leiomyoma']",1738,,,C0238197,,C7725,,,,,,
mondo:0002093,acanthoma,"['acanthoma (disease)', 'acanthoma']",174,,,C0846967,,C7419,,D049309,,,,0025432
mondo:0002095,vascular cancer,"['blood vessel neoplasm', 'blood vessel tumors', 'vascular tissue neoplasm', 'malignant tumour of pulmonary vein', 'blood vessel tumour (morphologic abnormality)', 'blood vessel tumor disorder', 'Haemangiomatous tumor', 'Haemangiomatous tumour', 'malignant vascular tumour', 'blood vessel tumors (morphologic abnormality)', 'blood vessel tumours', 'malignant neoplasm of vasculature', 'malignant blood vessel tumor', 'malignant vasculature neoplasm', 'pulmonary artery cancer', 'renal vein leiomyosarcoma', 'pulmonary artery malignant neoplasm', 'blood vessel tumor (morphologic abnormality)', 'malignant vascular neoplasm', 'pulmonary vein malignant neoplasm', 'blood vessel tumour', 'vascular tumors', 'malignant great vessel tumour', 'malignant tumor of pulmonary artery', 'blood vessel tumours (morphologic abnormality)', 'blood vessel tumour disorder', 'malignant blood vessel tumour', 'malignant vascular tumor', 'blood vessel tumor', 'malignant tumour of pulmonary artery', 'malignant blood vessel neoplasm', 'malignant tumor of pulmonary vein', 'neoplasm of great vessel', 'leiomyosarcoma of the renal vein', 'vascular tumours', 'cancer of vasculature']",175,,,,,C8538,,D009383,,,,
mondo:0002096,malignant conjunctival melanoma,"['conjunctival melanoma', 'malignant melanoma of conjunctiva', 'conjunctival malignant melanoma', 'melanoma of the conjunctiva', 'conjunctiva melanoma', 'malignant conjunctival melanoma', 'melanoma of conjunctiva', 'malignant conjunctiva melanoma', 'malignant melanoma of the conjunctiva', 'conjunctiva melanoma (disease)', 'CM']",1751,,617910,C0346360,,C4550,1000204,,,,,
mondo:0002098,facial nerve disorder,"['disorder of facial nerve', 'facial nerve disease', 'disease of facial nerve', 'facial nerve disease or disorder']",1756,,,C0015464,,C27594,,D005155,351.9,G51,,
mondo:0002099,Histoplasma capsulatum infectious disease,['Histoplasma capsulatum caused disease or disorder'],1759,,,,,,,,115.00,,,
mondo:0002100,cardiovascular cancer,"['malignant cardiovascular neoplasm', 'cardiovascular tumours', 'malignant neoplasm of cardiovascular system', 'malignant cardiovascular system neoplasm', 'cardiovascular neoplasm', 'cardiovascular tumors', 'cancer of cardiovascular system']",176,,,C3898472,,C114940,,,,,,
mondo:0002101,facial nerve neoplasm,"['VIIth cranial nerve neoplasms', 'facial nerve tumor', 'tumour of the seventh cranial nerve', 'seventh cranial nerve tumors', 'neoplasm of seventh cranial nerve', 'tumour of the Facial nerve', 'seventh cranial nerve neoplasms', 'facial nerve tumour', 'neoplasm of facial nerve', 'facial nerve tumors', 'tumour of Facial nerve', 'VIIth cranial nerve tumors', 'facial nerve neoplasms', 'VIIth cranial nerve tumours', 'neoplasm of Facial nerve', 'seventh cranial nerve tumour', 'facial nerve tumours', 'tumor of seventh cranial nerve', 'neoplasm of the seventh cranial nerve', 'seventh cranial nerve tumor', 'facial nerve neoplasm', 'tumor of facial nerve', 'tumour of facial nerve', 'tumor of Facial nerve', 'tumour of seventh cranial nerve', 'tumor of the seventh cranial nerve', 'neoplasm of the Facial nerve', 'seventh cranial nerve neoplasm', 'facial nerve neoplasm (disease)', 'tumor of the Facial nerve', 'seventh cranial nerve tumours']",1760,,,C1263899,,C5827,,,239.7,,,
mondo:0002102,cheilitis,['lip inflammation'],1762,,,C0007971,,C79545,,D002613,,,,0100825
mondo:0002103,factitious disorder,['Munchausen syndrome'],1766,,,,,C92198,,D009110,300.19,,,
mondo:0002104,conversion disorder,"['functional movement disorder', 'conversion hysterical neurosis', 'hysterical neurosis, conversion type', 'functional neurological disorder', 'FND', 'conversion hysteria or reaction']",1768,,,,,,,D003291,300.11,,,
mondo:0002105,toxic megacolon,,1770,,,C0025162,,,,D008532,564.7,K59.31,,
mondo:0002106,labyrinthine unilateral reactive loss,"['unilateral loss of labyrinthine reactivity', 'loss of labyrinthine reactivity, unilateral']",1776,,,C0155519,,,,,386.55,,,
mondo:0002107,unilateral hyperactive labyrinth,"['hyperactive unilateral labyrinthine dysfunction', 'hyperactive labyrinth, unilateral']",1777,,,C0155515,,,,,386.51,,,
mondo:0002108,thyroid cancer,"['malignant thyroid gland tumour', 'malignant neoplasm of the thyroid', 'thyroid gland cancer', 'malignant tumor of thyroid', 'malignant thyroid neoplasm', 'malignant thyroid tumor', 'malignant tumour of thyroid gland', 'cancer of thyroid gland', 'malignant neoplasm of thyroid gland', 'malignant neoplasm of thyroid', 'malignant tumor of the thyroid gland', 'malignant neoplasm of the thyroid gland', 'malignant tumour of the thyroid gland', 'malignant tumour of thyroid', 'malignant thyroid gland tumor', 'malignant tumor of the thyroid', 'malignant tumor of thyroid gland', 'malignant tumour of the thyroid', 'neoplasm of thyroid gland', 'malignant thyroid gland neoplasm', 'thyroid gland neoplasm', 'malignant thyroid tumour']",1781,,,CN221577,,C7510,,,193,,,
mondo:0002109,pituitary cancer,"['malignant neoplasm of pituitary', 'malignant neoplasm of the pituitary gland', 'malignant tumour of pituitary', 'malignant tumour of the pituitary', 'malignant pituitary gland neoplasm', 'pituitary gland neoplasm', 'malignant pituitary tumor', 'pituitary tumor, malignant', 'pituitary neoplasms, malignant', 'pituitary neoplasm', 'pituitary gland cancer', 'malignant pituitary gland tumour', 'malignant tumour of pituitary gland', 'malignant tumour of the pituitary gland', 'malignant tumor of pituitary gland', 'malignant pituitary neoplasm', 'malignant pituitary tumour', 'cancer of pituitary gland', 'malignant neoplasm of the pituitary', 'malignant tumor of the pituitary', 'malignant tumor of the pituitary gland', 'malignant pituitary gland tumor', 'malignant tumor of pituitary', 'malignant neoplasm of pituitary gland']",1785,,,C0496842,,C4769,0005578,,,,,
mondo:0002110,adrenal rest tumor,"['adrenal rest tumor', 'adrenal rest neoplasm']",1786,,,C0001630,,C2860,1000798,D000314,,,,
mondo:0002112,benign peritoneal mesothelioma,"['peritoneum benign mesothelioma', 'peritoneal adenomatoid tumor', 'mesothelioma of peritoneum', 'peritoneal adenomatoid tumour']",1789,,,,,C7354,,,,,,
mondo:0002113,peritoneal carcinoma,"['carcinoma of peritoneum', 'peritoneum carcinoma', 'primary peritoneal carcinoma']",1791,,,,,C40022,,,,,,
mondo:0002114,pancreas lymphoma,"['pancreatic lymphoma', 'lymphoma of the pancreas', 'lymphoma of pancreas', 'pancreas lymphoma']",1792,,,C1335307,,C5714,,,,,,
mondo:0002116,malignant exocrine pancreas neoplasm,"['malignant exocrine pancreas tumor', 'malignant tumor of exocrine pancreas', 'cancer of exocrine pancreas', 'malignant tumour of exocrine pancreas', 'malignant tumor of the exocrine pancreas', 'exocrine pancreas cancer', 'malignant neoplasm of the exocrine pancreas', 'pancreatic exocrine tumor', 'malignant neoplasm of exocrine pancreas', 'malignant exocrine pancreas neoplasm', 'tumour of exocrine pancreas', 'malignant exocrine pancreas tumour', 'malignant tumour of the exocrine pancreas', 'pancreatic exocrine tumour', 'tumor of exocrine pancreas']",1795,,,C0346648,,C7430,,,,,,
mondo:0002117,pancreas sarcoma,"['pancreatic sarcoma', 'pancreas sarcoma', 'sarcoma of the pancreas', 'sarcoma of pancreas']",1796,,,C1096346,,C5715,,,,,,
mondo:0002118,urinary system disorder,"['urinary disease', 'diseases, urologic', 'disease, urological', 'disease, urinary tract', 'non-neoplastic urinary tract disease', 'disorder of renal system', 'urinary tract diseases', 'urological disease', 'disorder of urinary system', 'urologic disease', 'diseases, urological', 'urological disorders', 'urological diseases', 'renal system disease or disorder', 'diseases, urinary tract', 'disease of renal system', 'renal system disease', 'urologic disorder', 'urinary tract disease', 'disease, urologic', 'urinary tract disorder']",18,,,C1335051,,C3430,,D014570,V47.4,,,
mondo:0002119,ossifying fibroma,"['juvenile ossifying fibroma', 'cemento-ossifying fibroma', 'fibro-osteoma', 'peripheral ossifying fibroma', 'fibroma, ossifying, benign', 'ossifying fibroma', 'Cementifying fibroma', 'ossifying fibroma (disease)']",180,,,C0206640,,C8422,0007412,D018214,,,,0030426
mondo:0002120,neuroendocrine carcinoma,"['neuroendocrine cancer', 'NEC', 'neuroendocrine carcinoma']",1800,,,C0206695,,C3773,,D018278,,,,
mondo:0002121,mononeuritis simplex,,1802,,,C0235880,,,,,355.9,,,
mondo:0002122,neuritis,['peripheral neuritis'],1803,,,C0027813,,C116381,,D009443,729.2,,,
mondo:0002123,calcinosis,"['macrocalcification', 'calcium deposit(s)', 'pathologically calcified structure', 'deposit(s), calcium', 'calcification', 'pathologic calcification']",182,,,,,C3672,0003837,D002114,275.49,,,0003761
mondo:0002124,secondary lacrimal atrophy,,1822,,,,,,,,375.14,,,
mondo:0002125,status epilepticus,"['GCSE', 'generalized convulsive status epilepticus', 'grand mal status', 'generalised convulsive status epilepticus', 'SE']",1824,,,C0038220,,C85079,0008526,D013226,,,,
mondo:0002127,urethral stricture,"['urethral stricture', 'urethral stricture (disease)']",1829,,,C0041974,,C79821,,D014525,598.9,,,0012227
mondo:0002128,mononeuritis multiplex,['mononeuritis multiplex'],1835,,,C0151295,,C70938,,,354.5,G58.7,,
mondo:0002129,bone cancer,"['bone cancer', 'malignant neoplasm of bone', 'malignant tumour of the bone', 'bone tumour', 'CA - bone cancer', 'malignant tumor of bone', 'bone tumor', 'malignant bone neoplasm', 'malignant osseous neoplasm', 'osseous tumour', 'malignant osseous tumor', 'malignant osseous tumour', 'osseous tumor', 'cancer of bone', 'malignant skeletal element neoplasm', 'skeletal element cancer', 'malignant tumor of the bone', 'malignant neoplasm of skeletal element', 'malignant neoplasm of the bone', 'malignant tumour of bone', 'malignant bone tumor', 'cancer of skeletal element', 'malignant bone tumour', 'bone neoplasm', 'cancer of the bone', 'osseous cancer']",184,,,,,C4016,,D001859,170.9,,,
mondo:0002130,upper limb mononeuronitis,"['mononeuritis simplex of forelimb', 'mononeuritis upper limb', 'forelimb mononeuritis simplex', 'mononeuritis of upper limb, unspecified', 'mononeuritis of upper limb']",1844,,,,,,,,354.9,,,
mondo:0002131,jaw cancer,"['malignant jaw skeleton neoplasm', 'malignant neoplasm of jaw skeleton', 'jaw neoplasm', 'neoplasm of jaw', 'jaw skeleton cancer', 'cancer of jaw skeleton']",1862,,,,,,0007333,D007573,,,,
mondo:0002132,skull cancer,"['malignant neoplasm of skull', 'malignant skull neoplasm', 'cancer of skull', 'skull cancer']",1863,,,C0037305,,C3375,,,,,,
mondo:0002133,chronic rheumatic pericarditis,"['rheumatic pericarditis, chronic']",1869,,,C0155561,,,,,393,I09.2,,
mondo:0002134,physiological sexual disorder,"['sexual disorders, physiological', 'sexual dysfunctions, physiological', 'sexual dysfunction', 'physiological sexual dysfunctions', 'physiological sexual dysfunction', 'Sex disorders', 'sexual disorder, physiological', 'physiological sexual disorder', 'physiological sexual disorders']",1876,,,C0549622,,,,D012735,,,,
mondo:0002135,optic nerve disorder,"['second cranial nerve disorder', 'disorder of the second nerve', 'cranial nerve II disease or disorder', 'disease of cranial nerve II', 'optic nerve disorder', 'cranial nerve II disease', 'optic neuropathy', 'disorder of cranial nerve II']",1891,,519351,C0029132,,C79698,,D009901,377.9,,,
mondo:0002136,eczematous dermatitis of eyelid,,1893,,,C0155177,,,,,373.31,,,
mondo:0002137,noninfectious dermatoses of eyelid,['non-infected eyelid dermatoses'],1894,,,C0155176,,,,,373.3,,,
mondo:0002138,allergic contact dermatitis of eyelid,"['contact and allergic dermatitis of eyelid', 'eyelid allergic contact dermatitis']",1895,,,C0155178,,,,,692.9,,,
mondo:0002139,sigmoid disease,,1897,,,C0037072,,,,D012810,,,,
mondo:0002140,vagina sarcoma,"['vagina sarcoma', 'vaginal sarcoma', 'sarcoma of the vagina', 'sarcoma of vagina']",1901,,,C0238519,,C7737,,,,,,
mondo:0002141,cutaneous undifferentiated pleomorphic sarcoma,"['malignant cutaneous fibrous histiocytoma', 'undifferentiated pleomorphic sarcoma of zone of skin', 'cutaneous unclassified pleomorphic sarcoma (formerly cutaneous)', 'cutaneous unclassified pleomorphic sarcoma (formerly cutaneous ""malignant fibrous histiocytoma"")', 'cutaneous unclassified pleomorphic sarcoma', 'malignant fibrous histiocytoma of the skin', 'zone of skin undifferentiated pleomorphic sarcoma', 'malignant skin fibrous histiocytoma', 'malignant fibrous histiocytoma of skin', 'cutaneous undifferentiated pleomorphic sarcoma', 'cutaneous unclassified pleomorphic sarcoma (formerly cutaneous ""MFH"")', 'cutaneous malignant fibrous histiocytoma']",1906,,,C1275254,,C5576,1000212,,171.9,,,
mondo:0002142,undifferentiated pleomorphic sarcoma,"['undifferentiated pleomorphic sarcoma/malignant fibrous histiocytoma/high-grade spindle cell sarcoma', 'malignant fibrohistiocytic tumours', 'Storiform-pleomorphic MFH', 'malignant fibrohistiocytic tumors', 'Storiform-pleomorphic fibrous histiocytoma', 'malignant fibrous histiocytoma', 'MFH', 'Unclassified Pleomorphic sarcoma (formerly ""malignant fibrous histiocytoma"")', 'undifferentiated pleomorphic soft tissue sarcoma', 'fibroxanthosarcoma', 'fibrous histiocytoma, malignant (morphologic abnormality)', 'malignant fibrous histiocytoma of the soft tissue and bone', 'unclassified pleomorphic sarcoma', 'fibrous histiocytoma, malignant', 'UPS', 'adult undifferentiated pleomorphic sarcoma', 'malignant fibrous cytoma', 'malignant fibrous histiocytoma of soft tissue and bone', 'malignant fibroxanthoma', 'fibroxanthosarcoma (morphologic abnormality)', 'histiocytoma, fibrous, malignant', 'adult unclassified pleomorphic sarcoma', 'adult malignant fibrous histiocytoma', 'undifferentiated pleomorphic sarcoma', 'Unclassified Pleomorphic sarcoma (formerly ""MFH"")', 'Storiform-pleomorphic malignant fibrous histiocytoma']",1907,,2023,,,C4247,1001972,D051677,171.9,,10025552,
mondo:0002143,vaginal yolk sac tumor,"['yolk sac tumour', 'yolk sac tumor', 'vaginal yolk Sac tumor', 'vaginal endodermal sinus tumor', 'vaginal yolk Sac tumour', 'vaginal yolk Sac neoplasm', 'vaginal endodermal sinus neoplasm', 'vaginal endodermal sinus tumour']",1910,,,C1336945,,C6379,,,,,,
mondo:0002145,disorder of sexual differentiation,"['sexual differentiation disorder', 'intersex', 'disorders of sex development', 'sex differentiation disease', 'disorder of sex differentiation', 'intersex conditions', 'CARD', 'sex differentiation disorder', 'differences of sex development', 'disorder of sexual differentiation', 'disorders of sex development (DSD)', 'DSD', 'conditions affecting reproductive development', 'disorder of sex development']",1923,,90771,CN757797,,C103186,,D012734,,,10070597,
mondo:0002146,hypogonadism,"['hypogonadotropism', 'gonadotropin deficiency']",1924,,,C0020619,,C9227,,D007006,253.4,,,
mondo:0002149,reproductive system cancer,"['reproductive organ cancer', 'cancer of reproductive organ', 'malignant reproductive organ neoplasm', 'reproductive tumor', 'cancer of reproductive system', 'malignant neoplasm of reproductive system', 'malignant reproductive system neoplasm', 'malignant neoplasm of reproductive organ', 'reproductive tumour']",193,,,C1334618,,C36076,,,,,,
mondo:0002150,hypothalamic disorder,"['disorder of hypothalamus', 'hypothalamus disease', 'hypothalamus disease or disorder', 'disease of hypothalamus']",1931,,,C0020655,,,,D007027,253.9,,,
mondo:0002152,intermittent squint,['intermittent heterotropia'],1942,,,C0152210,,,,,378.20,,,
mondo:0002153,telogen effluvium,,1943,,,C0263518,,C112200,,,704.02,L65.0,,
mondo:0002154,trichomoniasis,"['infections, Trichomonas', 'Trichomonas infection']",1947,,,C0040921,,C35720,,D014245,131.9,A59,,
mondo:0002155,cholecystitis,"['acute and chronic cholecystitis', 'gallstone cholecystitis', 'acalculous cholecystitis', 'acute on chronic cholecystitis', 'chronic cholecystitis', 'acute cholecystitis', 'gall bladder inflammation']",1949,,,,,C34465,,D002764,575.11,,,
mondo:0002156,fallopian tube disorder,"['disease of fallopian tube', 'disorder of fallopian tube', 'fallopian tube disorder', 'fallopian tube disease or disorder', 'fallopian tube disease']",1962,,,C0015556,,C26771,,D005184,,,,
mondo:0002158,fallopian tube cancer,"['malignant tumour of fallopian tube', 'malignant fallopian tube tumor', 'malignant neoplasm of uterine tube', 'malignant fallopian tube tumour', 'malignant tumour of fallopian tubes', 'fallopian tube malignant tumour', 'malignant tubal tumour', 'malignant tumour of the fallopian tube', 'malignant tumor of the fallopian tube', 'tumor, fallopian tube, malignant', 'fallopian tube malignant tumor', 'fallopian tube malignant neoplasm', 'fallopian tube cancer', 'malignant fallopian tube neoplasm', 'malignant tubal tumor', 'tumor of the fallopian tube', 'cancer of fallopian tube', 'cancer of fallopian tubes', 'malignant neoplasm of fallopian tube', 'tubal cancer', 'tumour of the fallopian tube', 'malignant tumor of fallopian tubes', 'malignant tumor of fallopian tube', 'malignant neoplasm of the fallopian tube', 'neoplasm, fallopian tube, malignant']",1964,,180242,CN200469,,C7480,,,183.2,,10025915,
mondo:0002159,fallopian tube leiomyosarcoma,"['fallopian tube leiomyosarcoma', 'leiomyosarcoma of fallopian tube']",1965,,,C1517116,,C40128,,,,,,
mondo:0002162,fallopian tube adenosarcoma,"['adenosarcoma of fallopian tube', 'fallopian tube mullerian adenosarcoma', 'fallopian tube Müllerian adenosarcoma', 'fallopian tube adenosarcoma', 'fallopian tube Mullerian adenosarcoma']",1973,,,C1517121,,C40125,,,,,,
mondo:0002163,thymus lipoma,"['lipoma of thymus', 'thymus lipoma', 'Thymolipomatous hamartoma', 'Thymolipoma']",1975,,,C1336744,,C6452,,,,,,
mondo:0002164,focal chorioretinitis,,1979,,,C0154870,,,,,363.00,,,
mondo:0002165,rectal neoplasm,"['neoplasm of rectum', 'tumor of the rectum', 'tumour of rectum', 'rectum neoplasm', 'rectal tumour', 'rectum tumor', 'rectal tumor', 'rectum neoplasm (disease)', 'neoplasm of the rectum', 'tumor of rectum', 'tumour of the rectum', 'rectum tumour', 'rectal neoplasm']",1984,,,C0034885,,C3350,,D012004,,,,
mondo:0002166,rectum lymphoma,"['rectum lymphoma', 'lymphoma of rectum', 'lymphoma of the rectum', 'rectal lymphoma', 'primary rectal lymphoma']",1988,,,C1335685,,C5553,,,,,,
mondo:0002167,rectum malignant melanoma,"['rectal melanoma', 'rectum melanoma (disease)', 'malignant melanoma of rectum', 'melanoma of the rectum', 'malignant melanoma of the rectum', 'melanoma of rectum', 'rectal malignant melanoma']",1992,,,C0349539,,C4640,,,,,,
mondo:0002168,rectum sarcoma,"['rectal sarcoma', 'rectum sarcoma', 'sarcoma of the rectum', 'sarcoma of rectum']",1995,,,C1335688,,C5548,,,,,,
mondo:0002169,rectum adenocarcinoma,"['adenocarcinoma of the rectum', 'rectum adenocarcinoma', 'read', 'adenocarcinoma - rectum', 'adenocarcinoma of rectum', 'rectal adenocarcinoma']",1996,,,C0149978,,C9383,0005631,,,,,
mondo:0002170,chronic eustachian salpingitis,"['chronic eustachian tube salpingitis', 'otosalpingitis, chronic', 'chronic otosalpingitis']",1999,,,C0155430,,,,,381.52,,,
mondo:0002171,giant cell tumor,"['giant cell tumor NOS (morphologic abnormality)', 'giant cell tumors', 'tumour of the giant cell', 'giant cell neoplasm', 'giant cell tumors (morphologic abnormality)', 'giant cell tumours (morphologic abnormality)', 'giant cell tumor', 'giant cell tumour NOS (morphologic abnormality)', 'giant cell tumours', 'giant cell tumor (morphologic abnormality)', 'giant cell tumour (morphologic abnormality)', 'giant cell tumor (qualifier value)', 'giant cell tumour (qualifier value)', 'tumor of the giant cell']",200,,,C0017525,,C3055,,D005870,,,,
mondo:0002172,otosalpingitis,"['pharyngotympanic tube inflammation', 'Eustachian salpingitis', 'Eustachian tube salpingitis']",2000,,,C0155428,,,,,381.50,H68.0,,
mondo:0002173,neuroma,,2001,,,C0027858,,C3275,,D009463,215.9,,,
mondo:0002174,preretinal fibrosis,"['macular retinal puckering', 'macular puckering of retina', 'cellophane maculopathy']",2006,,,,,,,D019773,362.89,,,
mondo:0002175,degeneration of macula and posterior pole,"['degeneration of macula or posterior pole', 'degeneration of macula and posterior pole of retina']",2007,,,C0339436,,,,,362.5,H35.3,,
mondo:0002177,hyperinsulinism,"['hyperinsulinism', 'hyperinsulinemia', 'hyperinsulinism (disease)']",2018,,,C0020459,,,,D006946,251.1,,,0000842
mondo:0002178,placenta cancer,"['placental tumours', 'malignant placenta tumour', 'malignant tumor of the placenta', 'malignant placenta neoplasm', 'primary malignant neoplasm of placenta', 'malignant placental tumour', 'placental cancer', 'malignant placental tumor', 'malignant tumour of the placenta', 'malignant tumour of placenta', 'malignant neoplasm of the placenta', 'placenta cancer', 'malignant placenta tumor', 'deciduoma, malignant', 'placental tumors', 'malignant tumor of placenta', 'cancer of placenta', 'malignant neoplasm of placenta', 'malignant placental neoplasm']",2021,,,C0153572,,C3555,,,239.5,,,
mondo:0002181,exostosis,"['bony outgrowth', 'osteophyte', 'exostosis', 'orbital exostosis', 'swimmer^s exostosis', 'bone spur']",203,,,C1956089,,C3029,,,726.91,,,
mondo:0002182,communication disorder,['communicative disorders'],2033,,,,,C2958,,D003147,307.9,,,
mondo:0002183,enthesopathy,"['disorder of enthesis', 'enthesis disease or disorder', 'enthesis disease', 'disease of enthesis']",204,,,C0242490,,,,D012216,726.90,,,
mondo:0002184,drug-induced hepatitis,['drug-induced chronic hepatitis'],2044,,,,,,1000905,,,,,
mondo:0002185,hyperostosis,"['hypertrophy of bone', 'bone hypertrophy', 'hypertrophy of bone (morphologic abnormality)']",205,,,C0020492,,C34712,,D015576,733.99,,,
mondo:0002186,acute maxillary sinusitis,"['acute antritis', 'maxillary sinusitis, acute']",2050,,,C0155804,,,,,461.0,J01.0,,
mondo:0002187,vulvar disease,"['vulvar disease', 'vulvar disorder']",2059,,,C0042994,,C27631,,D014845,,,,
mondo:0002188,vulvar nodular hidradenoma,"['vulvar nodular hidradenoma', 'nodular hidradenoma of mammalian vulva', 'mammalian vulva nodular hidradenoma']",2060,,,C1520091,,C40312,,,,,,
mondo:0002189,nodular hidradenoma,"['nodular hidradenoma', 'solid and cystic hidradenoma', 'eccrine nodular hidradenoma']",2061,,,,,C7568,,,,,,
mondo:0002190,vulvar syringoma,"['syringoma of mammalian vulva', 'vulvar syringoma', 'mammalian vulva syringoma']",2064,,,C1520099,,C40311,,,,,,
mondo:0002191,syringoma,"['syringoma', 'eccrine syringoma']",2065,,,C0206673,,C3761,,D018252,,,,
mondo:0002192,vulvar angiokeratoma,"['mammalian vulva angiokeratoma', 'mammalian vulva angiokeratoma of Fordyce']",2066,,,C1274281,,C8596,,,,,,
mondo:0002193,Bartholin gland benign neoplasm,"['tumour of Bartholin^s gland', 'Bartholin gland neoplasm', 'major vestibular gland benign neoplasm', 'tumor of Bartholin^s gland']",2068,,,,,C6434,,,,,,
mondo:0002194,vestibular papilloma,"['vulvar squamous papilloma', 'mammalian vulva squamous papilloma', 'vestibular papilloma']",2071,,,C1336982,,C6376,,,,,,
mondo:0002195,vulvar squamous neoplasm,"['vulvar squamous tumor', 'mammalian vulva squamous cell neoplasm', 'vulvar squamous tumour', 'vulvar squamous neoplasm']",2072,,,C1520097,,C40283,,,,,,
mondo:0002196,perinatal intestinal perforation,,2073,,,C0159006,,,,,777.6,P78.0,,
mondo:0002197,minor vestibular glands adenoma,"['adenoma of minor vestibular glands', 'minor vestibular gland adenoma']",2075,,,C1510791,,C40301,,,,,,
mondo:0002198,vulvar glandular neoplasm,"['vulvar glandular tumor', 'vulvar glandular tumour', 'mammalian vulva glandular cell neoplasm', 'vulvar glandular neoplasm']",2076,,,C1520082,,C40292,,,,,,
mondo:0002199,benign mixed tumor of the vulva,"['benign mixed tumor of the vulva', 'chondroid syringoma of the vulva']",2078,,,C1511091,,C40302,,,,,,
mondo:0002200,eccrine mixed tumor of skin,"['eccrine mixed tumour', 'benign mixed tumor of the skin', 'benign mixed tumor of skin (chondroid syringoma)', 'benign mixed tumour of the skin (chondroid syringoma)', 'benign mixed tumor of skin', 'benign mixed tumour of the skin', 'benign mixed tumour of skin (chondroid syringoma)', 'benign mixed tumour of skin', 'eccrine mixed tumour (morphologic abnormality)', 'mixed eccrine neoplasm of the skin', 'mixed tumor of the skin (chondroid syringoma)', 'mixed tumour of the skin (chondroid syringoma)', 'eccrine sweat gland mixed neoplasm', 'eccrine mixed tumor', 'chondroid syringoma', 'benign mixed tumor of the skin (chondroid syringoma)', 'eccrine mixed tumor (morphologic abnormality)']",2079,,,C0346026,,C4474,1000385,,,,,
mondo:0002201,vulvar trichoepithelioma,"['vulvar trichoepithelioma', 'mammalian vulva trichoblastoma', 'vulvar trichoblastoma']",2080,,,C1520100,,C40314,,,,,,
mondo:0002202,outlet dysfunction constipation,,2088,,,,,,,,564.02,K59.02,,
mondo:0002203,constipation disorder,"['constipation', 'colonic inertia', 'Dyschezia']",2089,,,,,C37930,,D003248,564.00,K59.0,,0002019
mondo:0002204,transient arthritis,['transient arthropathy'],2092,,,C3887596,,,,,716.40,,,
mondo:0002205,vulvar melanoma,"['malignant melanoma of vulva', 'vulvar melanoma', 'vulvar melanoma (disease)', 'mammalian vulva melanoma (disease)']",2093,,,C0241989,,C40329,,,,,,0030418
mondo:0002206,sweat gland cancer,"['malignant neoplasm of the sweat gland', 'malignant tumor of sweat gland', 'cancer of sweat gland', 'malignant tumor of the sweat gland', 'malignant neoplasm of sweat gland', 'sweat gland neoplasms, malignant', 'malignant sweat gland neoplasm', 'malignant tumour of sweat gland', 'sweat gland cancer', 'malignant tumour of the sweat gland']",2095,,,C1321904,,C4810,,,,,,
mondo:0002207,vulval Paget disease,"['vulval Paget^s disease', 'Paget disease of the vulva', 'Paget^s disease of the vulva', 'vulvar Paget^s disease', 'mammalian vulva Paget disease', 'vulva Paget^s disease', 'Paget^s disease of vulva', 'vulval Paget disease']",2097,,,C1275217,,C4027,,,233.39,,,
mondo:0002209,heel spur,"['calcaneal spur', 'calcaneus exostosis']",210,,,C0158322,,,,D036982,726.73,M77.3,,
mondo:0002211,B cell deficiency,"['immunoglobulin heavy chain deletion', 'B cell (antibody) deficiencies', 'deficiency of humoral immunity', 'B-cell deficiency', 'immunoglobulin heavy chain deficiency']",2115,,,,,C4799,,,279.03,,,
mondo:0002212,pneumonic tularemia,"['pulmonary tularemia', 'pneumonic tularaemia', 'bronchopneumonic tularemia']",2122,,,C0339946,,,,,021.2,,,
mondo:0002214,brain germinoma,"['brain germinoma (disease)', 'germinoma of brain', 'intracranial germinoma', 'germinoma of the brain']",2127,,,C1332606,,C6284,,,,,,
mondo:0002216,brain sarcoma,"['primary brain sarcoma', 'brain sarcoma', 'sarcoma of brain', 'sarcoma of the brain']",2132,,,C1332607,,C5154,,,,,,
mondo:0002217,central nervous system sarcoma,"['CNS sarcoma', 'sarcoma of the central nervous system', 'sarcoma of CNS', 'central nervous system sarcoma', 'sarcoma of central nervous system', 'sarcoma of the CNS']",2133,,,C1332892,,C5153,,,,,,
mondo:0002218,temporal lobe cancer,"['cancer of temporal lobe', 'malignant temporal lobe neoplasm', 'temporal lobe cancer', 'tumour of temporal lobe', 'temporal lobe neoplasm', 'malignant neoplasm of temporal lobe']",2135,,,C0153636,,,,,191.2,C71.2,,
mondo:0002219,paraurethral gland neoplasm,"['neoplasm of paraurethral glands', 'paraurethral gland tumour', 'tumor of the paraurethral gland', 'tumour of paraurethral gland', 'paraurethral gland neoplasm (disease)', 'tumour of the paraurethral gland', 'neoplasm of paraurethral gland', 'paraurethral gland tumor', 'tumor of paraurethral gland']",2139,,,C0341766,,,,,239.5,,,
mondo:0002220,tooth hard tissue disease,['teeth hard tissue disease'],214,,,C0155926,,,,,521.89,K03,,
mondo:0002221,urethral urothelial papilloma,"['urethral urothelial papilloma', 'urethra urothelial papilloma']",2140,,,C1519826,,C5061,,,,,,
mondo:0002222,urethra leiomyoma,"['leiomyoma of the urethra', 'urethra leiomyoma', 'leiomyoma of urethra', 'urethral leiomyoma']",2142,,,C1336888,,C6171,,,,,,
mondo:0002223,ovarian malignant mesothelioma,"['ovary malignant mesothelioma (disease)', 'ovarian malignant mesothelioma']",2143,,,C1518721,,C40444,,,,,,
mondo:0002224,malignant ovarian cyst,"['ovarian cyst (disease), malignant', 'malignant ovarian cyst']",2145,,,C0235770,,C3843,,,,,,
mondo:0002225,ovarian sarcoma,"['sarcoma of the ovary', 'sarcoma of ovary', 'ovarian sarcoma', 'ovary sarcoma']",2146,,,C0280746,,C8267,,,,,,
mondo:0002226,tuberculous oophoritis,,2148,,,C0275932,,,,,016.60,,,
mondo:0002227,ovarian lymphoma,"['ovary lymphoma', 'lymphoma of ovary', 'primary ovarian lymphoma', 'ovarian lymphoma']",2150,,,C1518720,,C40021,,,,,,
mondo:0002229,ovarian epithelial tumor,"['OVT', 'ovarian surface-epithelial stromal neoplasm', 'ovarian epithelial tumor', 'ovarian surface epithelial-stromal tumor', 'ovarian surface epithelial-stromal tumour', 'ovary epithelial neoplasm', 'epithelial tumor of ovary', 'ovary epithelial cancer', 'epithelial tumour of ovary', 'epithelial tumour of the ovary', 'epithelial neoplasm of ovary', 'epithelial tumor of the ovary', 'epithelial neoplasm of the ovary']",2152,,,C0341823,,C4381,,,239.5,,,
mondo:0002230,ovarian Wilms tumor,"['ovarian Wilms tumor', 'ovarian Wilms^ tumor', 'ovarian Wilms^ tumour', 'ovary Wilms tumour', 'ovary Wilms tumor', 'ovarian Wilms^ cancer']",2153,,,C1518746,,C40443,,,,,,
mondo:0002232,nasal cavity disorder,"['nasal cavity disease', 'nasal cavity disorder', 'disease of nasal cavity', 'nasal cavity disease or disorder', 'disorder of nasal cavity']",2163,,,C0339820,,C27102,,,,,,
mondo:0002233,enamel caries,"['simple dental cavity', 'primary dental caries', 'enamel dental caries', 'dental caries of enamel', 'dental caries limited to enamel']",217,,,C0266853,,,,,521.01,,,
mondo:0002234,vaginitis,"['vaginitis (disease)', 'vaginitis', 'vagina inflammation', 'vaginal inflammation', 'vaginal Inflammation']",2170,,,C0042267,,C26911,0005757,D014627,616.10,,,0030683
mondo:0002235,eyelid neoplasm,"['tumor of the eyelid', 'palpebral tumor', 'tumour of the eyelid', 'eyelid tumour', 'eyelid tumor', 'tumor of eyelid', 'tumour of eyelid', 'neoplasm of eyelid', 'neoplasm of the eyelid', 'eyelid neoplasm', 'palpebral tumour', 'eyelid neoplasm (disease)']",2173,,98580,C0015424,,C3031,1000934,D005142,,,,
mondo:0002236,ocular cancer,"['cancer of eyeball of camera-type eye', 'cancer of eye', 'neoplasm of eye', 'eye cancer', 'malignant tumor of eye', 'malignant eye neoplasm', 'malignant eyeball of camera-type eye neoplasm', 'eye neoplasm, malignant', 'malignant neoplasm of eye', 'neoplasm of eye proper', 'malignant ocular tumour', 'malignant eye tumor', 'ocular tumour', 'malignant neoplasm of the eye', 'malignant ocular neoplasm', 'malignant tumour of the eye', 'eye neoplasm', 'malignant neoplasm of eyeball of camera-type eye', 'cancer of the eye', 'malignant tumour of eye', 'malignant eye tumour', 'malignant tumor of the eye', 'malignant ocular tumor', 'ocular tumor']",2174,,,,,C4767,,D005134,239.89,,,
mondo:0002237,carbuncle,"['carbuncle and furuncle of upper arm and forearm', 'carbuncle and furuncle of neck', 'carbuncle and furuncle of hand', 'carbuncle and furuncle of gluteal region', 'carbuncle and furuncle of leg except foot', 'carbuncle and furuncle of foot', 'carbuncle and furuncle of buttock', 'carbuncle and furuncle of face', 'carbuncle and furuncle of any part of face except eye', 'carbuncle and furuncle of trunk']",2176,,,C0007078,,,1000674,D002270,680.9,,,
mondo:0002238,ascending colon cancer,"['cancer of ascending colon', 'malignant neoplasm of ascending colon', 'Ca ascending colon', 'malignant ascending colon neoplasm', 'malignant tumour of ascending colon', 'ascending colon cancer', 'malignant tumor of ascending colon', 'malignant neoplasm of right colon']",218,,,C0153439,,,,,153.6,,,
mondo:0002239,post-surgical hypoinsulinemia,['postsurgical hypoinsulinemia'],2181,,,C0154190,,,,,251.3,,,
mondo:0002240,acute perichondritis of pinna,"['perichondritis of auricle, acute', 'acute perichondritis of auricle']",221,,,C0155390,,,,,380.01,,,
mondo:0002241,factor XIII deficiency,['FXIIID'],,,,,,,,D005177,,,,
mondo:0002242,coagulation protein disease,"['coagulation factor deficiency syndrome', 'coagulation factor deficiency']",2212,,,C0600503,,C27215,,D020147,,,,
mondo:0002243,hemorrhagic disease,"['hemorrhagic diathesis', 'hemorrhagic disease', 'bleeding tendency', 'bleeding diathesis', 'bleeding predisposition', 'bleeding disorder']",2213,,,,,C115221,,D006474,287.9,,,
mondo:0002244,factor VII deficiency,"['deficiency, stable', 'F7 deficiency', 'factor VII deficiency', 'factor 7 deficiency']",,,,C0015503,,,,D005168,286.3,,,
mondo:0002245,blood platelet disease,"['platelet disorder', 'platelet abnormality']",,,,,,C131634,,D001791,,,,
mondo:0002246,perichondritis of auricle,"['perichondritis of pinna, unspecified', 'perichondritis and chondritis of pinna', 'perichondritis of pinna']",222,,,C0155389,,,,,380.00,,,
mondo:0002247,factor X deficiency,,,,,,,C131632,,D005171,,,,
mondo:0002249,thrombocytosis disease,"['Platelet count increased', 'thrombocytosis', 'Thrombocythaemia', 'elevated Platelet count']",2228,,,C0836924,,C35530,,D013922,289.9,,,
mondo:0002250,basilar artery insufficiency,['basilar artery syndrome'],223,,,C0004812,,C34413,,D014715,435.0,,,
mondo:0002251,hepatitis,"['chronic hepatitis', 'acute/subac. necrosis of liver', 'Hepatitides', 'acute and subacute liver necrosis', 'chronic persistent hepatitis', 'animal hepatitis', 'hepatitis', 'liver inflammation', 'acute hepatitis', 'Hepatitis']",2237,,,,,C3095,0008496,D006505,571.41,,,
mondo:0002252,granulomatous hepatitis,,2239,,,C0235369,,C27015,,,,,,
mondo:0002253,spondylosis,"['lumbar spondylosis with myelopathy', 'spondylosis with myelopathy', 'thoracic or lumbar spondylosis with myelopathy', 'spondylogenic compression of thoracic spinal cord', 'spondylogenic compression of lumbar spinal cord', 'lumbosacral spondylosis without myelopathy']",2247,,,C0038019,,,,D055009,721.9,M47,,
mondo:0002254,syndromic disease,"['clusters, symptom', 'symptom clusters', 'symptom cluster', 'syndrome associated with disease or disorder', 'syndromes', 'syndromic disease or disorder', 'syndromic disease', 'cluster, symptom', 'syndrome']",225,,,C0039082,,C28193,,D013577,,,,
mondo:0002255,hypertrophic elongation of cervix,,2251,,,C0020561,,,,,622.6,,,
mondo:0002256,cervix disorder,"['cervical disorder', 'uterine cervix disease', 'disorder of uterine cervix', 'disease of uterine cervix', 'uterine cervix disease or disorder']",2253,,,C0007867,,C40241,,D002577,,,,
mondo:0002257,ankylosis,"['ankylosis', 'ankylosis (disease)']",227,,,,,,,D000844,718.50,,,0031013
mondo:0002258,pharyngitis,"['acute sore throat', 'pharyngeal disorder', 'inflamed throat', 'chronic pharyngitis', 'throat inflammation', 'persistent sore throat', 'chronic sore throat', 'pharyngeal disease', 'Sore throat - chronic', 'pharyngitis - acute', 'chronic pharyn/nasopharyngitis', 'Sore throat', 'acute pharyngitis', 'chronic pharyngitis and nasopharyngitis']",2275,,,C0031350,,C26851,,D010612,478.20,,,
mondo:0002259,gonadal disorder,"['gonad disease or disorder', 'disease of gonad', 'gonad disease', 'gonadal disorders', 'disorder of gonad', 'gonadal disorder', 'disorder of gonads']",2277,,,C0018050,,C26786,,D006058,,,,
mondo:0002260,hidradenitis,"['apocrine sweat gland', 'apocrine sweat gland inflammation', 'Hydradenitis']",2282,,,C0085160,,C32132,,D016575,705.83,,,
mondo:0002261,keratopathy,,2283,,,C0235270,,C27012,,,,,,
mondo:0002262,capillary lymphangioma,"['capillary lymphangioma', 'cutaneous lymphangioma']",2286,,,C1333176,,C27509,,,,,,
mondo:0002263,female reproductive system disorder,"['female reproductive system disorder', 'disorder of female reproductive system', 'female reproductive disease', 'gynaecological disease', 'disease of female reproductive system', 'female reproductive system disease', 'female reproductive system disease or disorder']",229,,,,,C27020,,D005831,629.9,,,
mondo:0002265,stereotypic movement disorder,"['stereotyped repetitive movements', 'stereotypy habit disorder', 'stereotyped repetitive movements NOS (finding)']",2303,,,,,,,D019956,307.3,,,
mondo:0002266,malt worker^s lung,"['Malt-workers^ lung', 'malt worker lung', 'malt workers lung', 'Aspergillus caused extrinsic allergic alveolitis', 'alveolitis due to aspergillus clavatus', 'Malt workers^ lung']",2314,,,C0155888,,,,,495.4,,,
mondo:0002267,obstructive lung disease,['respiratory airway obstruction'],2320,,,C0600260,,,,D008173,,,,
mondo:0002268,dyspepsia,"['dyspepsia, indigestion', 'indigestion']",2321,,,,,C26756,0008533,D004415,,,,
mondo:0002269,gastroenteritis,"['intestine inflammation', 'infectious colitis, enteritis and gastroenteritis', 'cholera morbus']",2326,,,C0017160,,C34632,1001463,D005759,558.9,,,
mondo:0002270,viral gastritis,"['viral gastritis', 'Viruses caused gastritis (disease)']",2327,,,C0563238,,C27184,,,008.8,,,
mondo:0002271,colon adenocarcinoma,"['COAD', 'adenocarcinoma of the colon', 'colonic adenocarcinoma', 'adenocarcinoma of colon', 'adenocarcinoma - colon', 'colon adenocarcinoma']",234,,,C0338106,,C4349,1001949,,,,,
mondo:0002272,polyclonal hypergammaglobulinemia,['polyclonal hypergammaglobulinemia'],2344,,,C0154254,,C35885,,,273.0,D89.0,,
mondo:0002273,plasma protein metabolism disease,,2345,,,,,,,,273.8,,,
mondo:0002274,monoclonal paraproteinemia disease,"['monoclonal paraproteinemia', 'monoclonal paraproteinaemia', 'paraproteinaemia']",2346,,,C0026471,,C35878,,,273.1,,,0031047
mondo:0002275,generalized atherosclerosis,"['generalized atherosclerosis', 'generalized and unspecified atherosclerosis', 'generalised and unspecified atherosclerosis']",2347,,,C0017327,,C35767,,,440.9,I70.91,,
mondo:0002277,arteriosclerosis disorder,"['vascular sclerosis', 'arteriosclerosis', 'arteriosclerotic cardiovascular disease', 'arterial sclerosis', 'cardiovascular arteriosclerosis']",2349,,,C3665365,,C34403,0009086,D001161,440,,,0002634
mondo:0002278,benign colon neoplasm,"['benign colon neoplasm', 'colonic tumour', 'benign colon tumor', 'benign colon tumour', 'benign colonic tumour', 'colon neoplasm', 'benign neoplasm of colon', 'benign tumor of colon', 'benign tumour of colon', 'benign colonic tumor', 'colonic Mass', 'colonic benign neoplasm', 'benign tumor of the colon', 'colonic tumor', 'colon benign neoplasm', 'benign tumour of the colon', 'benign neoplasm of the colon', 'benign colonic neoplasm']",235,,,C0004991,,C2894,,,211.3,,,
mondo:0002279,iron metabolism disease,"['iron metabolism disorder', 'disorders, iron metabolism', 'disorder, iron metabolism', 'iron disorder', 'metabolism disorder, iron', 'disorder of iron metabolism', 'metabolism disorders, iron']",2351,,,C0012715,,,,D019189,275.0,E83.1,,
mondo:0002280,anemia,"['anemia (disease)', 'anemia', 'anaemia (disease)']",2355,,,,"['-0.4797', '0.4106', '0.0121', '0.1682', '0.7563', '0.3274', '-0.2896', '0.4307', '-0.2028', '-0.4648', '0.6855', '-0.1448', '0.257', '0.3257', '-0.9697', '-0.0842', '-0.6294', '0.3767', '-0.2708', '-0.4138', '-0.1288', '-0.518', '0.4426', '0.014', '0.9336', '-0.3586', '0.0106', '-0.1967', '0.4172', '0.09894', '0.2954', '0.1416', '0.255', '0.695', '0.2024', '-0.3147', '-0.631', '-0.4526', '0.4468', '-0.396', '-0.4944', '0.2427', '-0.00633', '-0.3945', '-0.677', '-0.8657', '0.1299', '0.443', '0.3235', '-0.2416', '0.515', '0.49', '0.575', '-0.1942', '0.575', '-0.7617', '-0.02873', '0.403', '-1.098', '0.1946', '-0.06152', '0.3982', '-0.2142', '-0.5103', '-0.03622', '0.2178', '0.1868', '0.921', '-0.537', '0.872', '0.834', '-0.3267', '-0.5957', '-0.8945', '0.2368', '0.93', '0.2339', '0.1373', '0.05936', '0.2615', '0.1007', '-0.3184', '0.268', '0.1428', '0.639', '-0.2017', '-0.633', '0.3835', '0.7856', '-0.3882', '0.7373', '0.345', '-0.1078', '0.00739', '0.656', '0.823', '0.2214', '-0.0443', '0.2438', '-0.603']",C2869,0004272,D000740,285.9,,,0001903
mondo:0002281,macrocytic anemia,"['macrocytic anaemia (disease)', 'macrocytic anaemia of unspecified cause', 'macrocytic Anemia', 'anemia macrocytic', 'macrocytic anemia (disease)', 'macrocytic anemia of unspecified cause', 'macrocytic Anaemia', 'macrocytic anemia', 'D22S750', 'D22S676', 'anaemia macrocytic']",2361,,,C0002886,,C34381,,D000748,,,,0001972
mondo:0002282,West Nile fever,['West Nile virus caused disease or disorder'],2366,,,,,,,D014901,066.40,,,
mondo:0002283,neuroaxonal dystrophy,,2367,,,C0338473,,C161542,,D019150,,,,
mondo:0002285,pupil disorder,"['pupil disease or disorder', 'disease of pupil', 'pupil disease', 'disorder of pupil', 'pupillary disorder']",238,,,C0034124,,,,,,,,
mondo:0002286,renal artery disease,"['vascular disorder of kidney', 'renal vascular disease']",2388,,,C3640053,,C101254,,,593.81,,,
mondo:0002287,glandular cystitis,['cystitis glandularis'],2392,,,C0268837,,C39860,,,595.89,,,
mondo:0002289,iris disorder,"['disorder of iris', 'disease of iris', 'iris disorder', 'iris disease', 'iris disease or disorder']",240,,,C0022078,,C34737,,D007499,,,,
mondo:0002290,clitoris cancer,"['clitoral Ca', 'malignant clitoral neoplasm', 'malignant tumour of the clitoris', 'cancer of clitoris', 'malignant clitoris tumour', 'malignant neoplasm of clitoris', 'carcinoma of clitoris', 'clitoris cancer', 'malignant clitoris neoplasm', 'malignant neoplasm of the clitoris', 'malignant tumour of clitoris', 'malignant clitoral tumor', 'malignant tumor of clitoris', 'malignant tumor of the clitoris', 'malignant clitoral tumour', 'malignant clitoris tumor']",2401,,,C0153589,,C3557,,,184.3,,,
mondo:0002291,cutaneous granular cell tumor,"['granular cell tumour of skin', 'cutaneous granular cell tumor', 'cutaneous granular cell neoplasm', 'granular cell skin tumour', 'granular cell tumour of the skin', 'skin granular cell neoplasm', 'skin granular cell tumour', 'granular cell neoplasm of skin', 'granular cell tumor of the skin', 'granular cell tumour of zone of skin', 'zone of skin granular cell tumour', 'skin granular cell tumor', 'granular cell tumor of zone of skin', 'granular cell neoplasm of the skin', 'zone of skin granular cell tumor', 'granular cell skin tumor', 'granular cell tumor of skin']",2410,,,C0346060,,C5617,,,215.9,,,
mondo:0002293,cutaneous ganglioneuroma,"['skin ganglioneuroma', 'ganglioneuroma of the skin', 'ganglioneuroma of skin', 'cutaneous ganglioneuroma']",2425,,,C0346063,,C4481,,,,,,
mondo:0002295,skin glomus tumor,"['glomus tumor of the skin', 'glomus tumor of skin', 'glomus tumour of the skin', 'glomus neoplasm of the skin', 'glomus skin tumor', 'glomus neoplasm of skin', 'zone of skin glomus tumour', 'glomus tumour of skin', 'glomus skin tumour', 'glomus skin neoplasm', 'skin glomus neoplasm', 'zone of skin glomus tumor']",2430,,,C0346083,,C4491,,,,,,
mondo:0002297,epidermal appendage tumor,"['adnexal neoplasm of the skin', 'neoplasm of cutaneous appendage', 'tumour of Epidermal appendage', 'Epidermal appendage neoplasm', 'tumour of cutaneous appendage', 'neoplasm of skin with adnexal differentiation', 'tumour of skin appendage', 'tumor of skin appendage', 'skin appendage tumor', 'tumor of cutaneous appendage', 'cutaneous appendage neoplasm (disease)', 'adnexal tumour of skin', 'tumor of the skin appendage', 'skin appendage neoplasm', 'adnexal neoplasm of skin', 'Epidermal appendage tumor', 'tumour of the skin appendage', 'Epidermal appendage tumour', 'cutaneous appendage tumor', 'adnexal tumor of skin', 'adnexal tumour of the skin', 'skin appendage tumour', 'tumor of Epidermal appendage', 'cutaneous adnexal neoplasm', 'adnexal tumor of the skin', 'cutaneous appendage tumour', 'neoplasm of the skin appendage', 'neoplasm of Epidermal appendage', 'neoplasm of skin appendage']",2433,,,C0345988,,C4463,,,239.2,,,
mondo:0002298,cutaneous glomangioma,"['zone of skin glomangioma', 'skin glomangioma', 'glomangioma of the skin', 'glomangioma of skin', 'cutaneous glomangioma']",2435,,,C1275226,,C6750,,,,,,
mondo:0002299,glomangioma,['glomangioma'],2436,,,C0334421,,C4222,,,,,,
mondo:0002300,dermis tumor,"['dermis neoplasm (disease)', 'dermal tumour', 'tumor of the dermis', 'dermal tumor', 'neoplasm of the dermis', 'tumour of the dermis', 'dermal neoplasm', 'neoplasm of dermis', 'tumour of dermis', 'dermis tumor', 'tumor of dermis']",2438,,,C0346041,,C4475,,,,,,
mondo:0002301,frontal sinus squamous cell carcinoma,"['epidermoid carcinoma of the frontal sinus', 'epidermoid carcinoma of frontal sinus', 'frontal sinus epidermoid carcinoma', 'squamous cell carcinoma of frontal sinus', 'squamous cell carcinoma of the frontal sinus', 'frontal sinus squamous cell carcinoma']",2441,,,C1333646,,C6067,,,,,,
mondo:0002303,central retinal vein occlusion,"['central retinal Venous occlusion', 'central retinal vein retinal vein occlusion', 'retinal vein occlusion of central retinal vein']",2450,,411527,C0154841,,C118859,,,362.35,,,
mondo:0002304,protein S deficiency,"['Protein S deficiency', 'Protein S deficiency disease']",2451,,,C0242666,,C99026,,D018455,289.81,,,
mondo:0002305,thrombophilia,"['hypercoagulability', 'hypercoagulability state', 'excessive blood clotting', 'hypercoagulable']",2452,,64738,C0398623,,C84479,,D019851,286.9,,,
mondo:0002306,angular blepharoconjunctivitis,,2455,,,C0155149,,,,,372.21,,,
mondo:0002307,blepharoconjunctivitis,,2456,,,C0005743,,C34430,,,372.20,H10.5,,
mondo:0002308,giant papillary conjunctivitis,['GPC'],2457,,,C0009769,,C34507,,,372.39,,,
mondo:0002309,papillary conjunctivitis,,2458,,,C0854165,,C35616,,,372.39,,,
mondo:0002310,anterior dislocation of lens,,2460,,,C0155372,,,,,379.33,,,
mondo:0002311,retinal vascular disorder,"['retina circulation disorder', 'retinal vascular disorder']",2462,,,C0154833,,C35170,,,362.13,,,
mondo:0002312,opportunistic mycosis,"['opportunistic mycoses', 'opportunistic systemic mycoses']",2473,,,C0029119,,,,,118,,,
mondo:0002313,vernal conjunctivitis,,2474,,,C0009773,,C34508,,,372.13,H10.44,,
mondo:0002314,chronic conjunctivitis,"['chronic conjunctivitis, unspecified', 'conjunctivitis (disease), chronic', 'chronic conjunctivitis']",2475,,,C0155145,,C35197,,,372.10,H10.4,,
mondo:0002316,motor peripheral neuropathy,"['neuropathic muscular atrophy', 'HSMN', 'HSMN - hereditary sensory and motor neuropathy', 'hereditary motor and sensory neuropathy', 'peripheral motor neuropathy']",2477,,,C0235025,,C75467,,D015417,356.9,,,
mondo:0002317,central nervous system origin vertigo,"['vertigo of central origin', 'central vestibular vertigo']",2479,,,C0155503,,,,,386.2,,,
mondo:0002318,trachea leiomyoma,"['leiomyoma of trachea', 'tracheal tumor', 'trachea neoplasm', 'tracheal tumour', 'leiomyoma of the trachea', 'tracheal leiomyoma', 'trachea leiomyoma', 'tracheal neoplasm']",248,,,C1336772,,C6049,,,,,,
mondo:0002319,phosphorus metabolism disease,"['phosphorus disorder', 'phosphorus metabolic disorder', 'phosphorus metabolism disorder', 'disorder of phosphorus metabolism']",2485,,,C0031707,,C97095,,D010760,275.3,E83.3,,
mondo:0002320,congenital nervous system disorder,"['congenital abnormality of the nervous system', 'congenital nervous system disorder', 'congenital neurologic anomaly']",2490,,,,,C97172,,,742,,,
mondo:0002321,sensory peripheral neuropathy,"['peripheral sensory neuropathy', 'sensory nerve peripheral neuropathy', 'peripheral neuropathy of sensory nerve', 'sensory neuropathy']",2491,,,C0151313,,C3501,,,356.9,,,
mondo:0002322,angiodysplasia,"['angiodysplasia of stomach and duodenum with hemorrhage', 'angiodysplasia of stomach and duodenum with haemorrhage']",2494,,,C0085411,,,,D016888,537.83,,,
mondo:0002323,cherry hemangioma,"['Senile hemangioma', 'cherry hemangioma', 'Senile naevus of skin', 'Senile angioma', 'cherry angioma']",2495,,,C0343082,,C4390,,,,,,
mondo:0002325,"tooth erosion, non-bacterial","['localized erosion', 'tooth erosion', 'generalised erosion', 'localised erosion', 'generalized erosion']",2498,,,C0040436,,,,D014077,521.35,,,
mondo:0002326,alcohol-induced mental disorder,,251,,,,,,,,291.89,,,
mondo:0002327,intracranial cavernous angioma,"['intracranial cavernoma', 'intracranial cavernous angioma', 'intracranial cavernous hemangioma']",2516,,,C1334237,,C5432,,,,,,
mondo:0002328,intracranial hemangioma,"['hemangioma of intracranial structures', 'brain hemangioma', 'hemangioma of brain', 'angioma of intracranial structure', 'intracranial hemangioma', 'hemangioma of the intracranial structure', 'angioma of the intracranial structure', 'intracranial angioma', 'intracranial structure hemangioma', 'hemangioma of intracranial structure']",2517,,,C0154050,,C3633,,,228.02,D18.02,,
mondo:0002329,testicular disorder,"['testicular disorder', 'testicular disease', 'disease of testis', 'testis disease or disorder', 'testis disease', 'testis disorder', 'disorder of testis']",2519,,,C0039584,,C26890,,D013733,608.89,,,
mondo:0002330,alcoholic psychosis,['alcoholic psychoses'],252,,,,,,1001260,D011604,291.9,,,
mondo:0002331,nephrosis,['Nephroses'],2527,,,C0027720,,,,D009401,,,,
mondo:0002332,splenic disorder,"['disease of spleen', 'Dyssplenism', 'spleen disease or disorder', 'spleen disease', 'disorder of spleen', 'spleen disorder']",2529,,,C0037997,,C35823,0009002,D013158,289.50,D73,,
mondo:0002333,splenic abscess,"['splenic abscess', 'splenic abscess (disease)']",2530,,,C0272412,,C35347,,,289.59,D73.3,,0025059
mondo:0002334,hematopoietic and lymphoid system neoplasm,"['haematopoietic neoplasm', 'tumor of hematopoietic system', 'hematopoietic and lymphoid system tumor', 'haematological tumours', 'hematopoietic system tumor', 'malignant hematopoietic neoplasm (morphologic abnormality)', 'neoplasm of blood', 'hematological tumors', 'neoplasm of hematopoietic system', 'haematopoietic system tumour', 'hematopoietic tumors', 'tumour of blood', 'blood tumour', 'haematopoietic neoplasm (morphologic abnormality)', 'tumor of blood', 'blood neoplasm (disease)', 'haematopoietic tumours', 'haematopoietic and lymphoid system tumour', 'hematologic neoplasm', 'hematopoietic neoplasm', 'malignant haematopoietic neoplasm', 'hematopoietic and lymphoid system neoplasm', 'haematopoietic system neoplasm', 'haematopoietic cancer', 'hematologic malignancy', 'malignant haematopoietic neoplasm (morphologic abnormality)', 'tumour of haematopoietic system', 'hematopoietic neoplasm (morphologic abnormality)', 'blood cancer', 'neoplasm of haematopoietic system', 'hematologic cancer', 'blood tumor', 'hematopoietic cancer']",2531,,,C1512393,,C35813,,D019337,,,,
mondo:0002335,chronic inflammatory demyelinating polyneuritis,['chronic inflammatory demyelinating polyneuropathy'],2536,,,,,C84636,,D020277,357.81,G61.81,,
mondo:0002337,intra-abdominal hemangioma,"['abdominal cavity hemangioma', 'hemangioma of abdominal cavity', 'intra-abdominal hemangioma', 'hemangioma of intra-abdominal structure', 'hemangioma, intra-abdominal', 'hemangioma of intra-abdominal structures']",254,,,C0154052,,C3635,,,228.04,D18.03,,
mondo:0002338,extratemporal epilepsy,['extratemporal epilepsy'],2544,,,C0270849,,C7760,,,345.80,,,
mondo:0002340,tactile epilepsy,,2550,,,C0393724,,C4687,,,,,,
mondo:0002341,granulomatous angiitis,['Granulomatous arteritis'],2555,,,C0018202,,C34653,,D020293,,,,
mondo:0002342,chondromalacia,,2557,,,C0085700,,,,,733.92,M94.2,,
mondo:0002343,splenic hemangioma,"['spleen hemangioma', 'spleen angioma', 'angioma of spleen', 'splenic hemangioma', 'angioma of the spleen', 'hemangioma of the spleen', 'splenic angioma', 'hemangioma of spleen']",256,,,C0685201,,C8541,,,,,,
mondo:0002345,cervicitis,"['cervicitis', 'cervicitis (disease)']",2568,,,,,C26716,,D002575,616.0,,,0030160
mondo:0002347,barbiturate dependence,,2575,,,,,,,,304.13,,,
mondo:0002350,familial nephrotic syndrome,"['hereditary nephrotic syndrome', 'congenital nephrotic syndrome']",2590,,,CN043611,,C35337,,,,,,
mondo:0002351,glottis cancer,"['malignant glottis neoplasm', 'malignant glottis tumour', 'malignant neoplasm of glottis', 'malignant tumour of the glottis', 'malignant tumor of glottis', 'malignant tumor of the glottis', 'malignant neoplasm of the glottis', 'glottis cancer', 'Ca larynx - glottis', 'cancer of glottis', 'malignant tumour of glottis', 'malignant glottis tumor']",2595,,,C0153483,,C3544,,,161.0,,,
mondo:0002352,larynx cancer,"['malignant neoplasm of the larynx', 'malignant larynx neoplasm', 'malignant laryngeal tumor', 'malignant laryngeal neoplasm', 'malignant tumor of the larynx', 'malignant tumor of larynx', 'larynx cancer', 'malignant larynx tumor', 'malignant larynx tumour', 'malignant neoplasm of larynx', 'malignant tumour of larynx', 'cancer of larynx', 'malignant laryngeal tumour', 'malignant tumour of the larynx']",2596,,,C0007107,,C7484,1000354,,161.9,,,
mondo:0002353,glottis neoplasm,"['glottis tumor', 'glottis neoplasm (disease)', 'neoplasm of glottis', 'tumour of glottis', 'glottis neoplasm', 'neoplasm of the glottis', 'tumor of the glottis', 'tumor of glottis', 'glottis tumour', 'tumour of the glottis']",2597,,,C0345713,,C4425,,,,,,
mondo:0002354,benign laryngeal neoplasm,"['benign laryngeal neoplasm', 'benign larynx neoplasm', 'benign tumour of the larynx', 'benign laryngeal tumor', 'laryngeal benign neoplasm', 'benign neoplasm of the larynx', 'benign tumor of the larynx', 'benign larynx tumor', 'larynx neoplasm', 'larynx benign neoplasm', 'benign tumour of larynx', 'laryngeal neoplasm, benign', 'laryngeal tumour', 'laryngeal tumor', 'benign larynx tumour', 'benign tumor of larynx', 'benign laryngeal tumour', 'benign neoplasm of larynx']",2598,,,C0153952,,C3601,,,212.1,,,
mondo:0002355,glottis carcinoma,"['glottic carcinoma', 'cancer of the glottis', 'glottic throat cancer', 'glottis carcinoma', 'glottis cancer', 'carcinoma of the glottis', 'cancer of glottis', 'carcinoma of glottis']",2599,,,C0740083,,C4923,,,,,,
mondo:0002356,pancreas disorder,"['pancreatic disease', 'pancreas disease', 'disease of pancreas', 'pancreatic disorder', 'pancreas disease or disorder', 'disease, pancreatic', 'disorder of pancreas', 'diseases, pancreatic']",26,,,,,C26842,,D010182,577.9,,,
mondo:0002357,hepatic flexure cancer,"['malignant neoplasm of hepatic flexure of colon', 'malignant tumor of hepatic flexure', 'hepatic flexure of colon cancer', 'cancer of hepatic flexure of colon', 'malignant tumour of hepatic flexure', 'Ca hepatic flexure - colon', 'malignant hepatic flexure of colon neoplasm', 'malignant neoplasm of hepatic flexure']",260,,,C0153433,,,,,153.0,,,
mondo:0002358,laryngeal carcinoma,"['larynx carcinoma', 'carcinoma of the larynx', 'carcinoma of larynx', 'cancer of larynx', 'cancer of the larynx', 'laryngeal cancer', 'laryngeal carcinoma', 'laryngeal throat cancer']",2600,,,C0595989,,C4855,,,,,,
mondo:0002359,periosteal chondroma,"['juxtacortical chondroma', 'periosteal chondroma', 'juxtacortical chondroma (morphologic abnormality)']",2601,,,C0334548,,C4302,,,,,,
mondo:0002360,chondroma,"['central chondroma', 'chondroma, benign', 'chondroma']",2602,,,C0936248,,C53459,,D002812,,,,
mondo:0002361,transverse colon cancer,"['cancer of transverse colon', 'malignant neoplasm of transverse colon', 'malignant tumour of transverse colon', 'malignant transverse colon neoplasm', 'malignant tumor of transverse colon', 'transverse colon cancer', 'Ca transverse colon']",261,,,C0153434,,,,,153.1,,,
mondo:0002362,serous surface papilloma,"['serous surface papilloma NOS (morphologic abnormality)', 'serous surface papilloma', 'serous surface papilloma (morphologic abnormality)']",2614,,,C0334360,,C4181,,,,,,
mondo:0002363,papilloma,"['papillomatosis NOS (morphologic abnormality)', 'papilloma, benign', 'papilloma (except papilloma of bladder M-81201) (morphologic abnormality)', 'papilloma']",2615,,,C0030354,,C7440,,D010212,,,,
mondo:0002365,kidney hemangiopericytoma,"['kidney spindle cell tumor', 'hemangiopericytoma of the kidney', 'kidney spindle cell tumour', 'hemangiopericytoma of kidney', 'renal hemangiopericytoma', 'kidney hemangiopericytoma']",262,,,C0346256,,C4527,,,,,,
mondo:0002366,autonomic nervous system neoplasm,"['autonomic nervous system tumor', 'autonomic nervous system neoplasms', 'neoplasm of autonomic nervous system', 'neoplasm of the autonomic nervous system', 'tumor of the autonomic nervous system', 'tumour of the autonomic nervous system', 'tumour of autonomic nervous system', 'autonomic nervous system neoplasm', 'autonomic nervous system neoplasm (disease)', 'autonomic nervous system tumour', 'tumor of autonomic nervous system']",2621,,,C1332356,,C5112,,,,,,
mondo:0002367,kidney cancer,"['malignant neoplasm of kidney except pelvis', 'malignant renal neoplasm', 'kidney cancer', 'malignant neoplasm of kidney', 'cancer of kidney', 'malignant kidney tumor', 'malignant neoplasm of the kidney', 'malignant renal tumor', 'malignant renal tumour', 'malignant tumour of the kidney', 'malignant tumor of the kidney', 'malignant tumour of kidney', 'malignant kidney neoplasm', 'malignant tumor of kidney', 'malignant kidney tumour']",263,,,CN881103,,C7548,,D007680,189.0,,,
mondo:0002368,papillary serous cystadenocarcinoma,"['papillary serous cystadenocarcinoma', 'serous surface papillary carcinoma (morphologic abnormality)', 'papillary serous carcinoma', 'papillary serous adenocarcinoma', 'micropapillary serous carcinoma']",2632,,,C0334359,,C8377,,,,,,
mondo:0002369,cystadenoma,"['cystadenoma, benign', 'cystadenoma (morphologic abnormality)', 'cystoma', 'cystadenoma']",2634,,,C0010633,,C2972,,D003537,,,,
mondo:0002370,ovarian Brenner tumor,"['benign ovarian Brenner tumour', 'Brenner tumor', 'Brenner neoplasm of ovary', 'ovarian Brenner neoplasm', 'Brenner tumour of the ovary', 'Brenner neoplasm of the ovary', 'ovarian Brenner tumor', 'Brenner tumor of the ovary', 'benign ovarian Brenner tumor', 'Brenner tumour of ovary', 'Brenner tumor of ovary', 'ovary Brenner tumour', 'Brenner tumour', 'ovary Brenner tumor']",2636,,,,,C3872,1000112,,,,,
mondo:0002371,breast pericanalicular fibroadenoma,"['breast pericanalicular fibroadenoma', 'pericanalicular fibroadenoma (morphologic abnormality)', 'pericanalicular breast fibroadenoma', 'pericanalicular fibroadenoma of the breast', 'pericanalicular fibroadenoma of breast', 'pericanalicular fibroadenoma']",2639,,,C0334497,,C4272,,,,,,
mondo:0002372,ovarian monodermal and highly specialized teratoma,"['ovarian monodermal and highly specialized teratoma', 'ovarian germ cell monodermal and highly specialised teratoma', 'ovarian germ cell monodermal and highly specialized teratoma']",2641,,,C0280134,,C8113,,,,,,
mondo:0002373,benign mesothelioma,"['benign tumour of mesothelium', 'mesothelioma, benign', 'benign tumor of mesothelium', 'benign tumour of mesothelial tissue']",2645,,,C0348424,,C3234,,D008654,215.9,C45,,
mondo:0002375,sebaceous adenoma,"['adenoma of sebaceous gland', 'sebaceous gland adenoma', 'adenoma, sebaceous, benign', 'sebaceous adenoma (morphologic abnormality)', 'skin appendage sebaceous adenoma', 'adenoma of the sebaceous gland']",2648,,,C1368816,,C4174,,,,,,
mondo:0002376,spleen angiosarcoma,"['splenic angiosarcoma', 'spleen angiosarcoma (disease)', 'angiosarcoma of the spleen', 'angiosarcoma of spleen', 'splenic hemangiosarcoma', 'hemangiosarcoma of spleen', 'hemangiosarcoma of the spleen']",265,,,C0346424,,C4564,,,159.1,,,
mondo:0002377,breast intracanalicular fibroadenoma,"['intracanalicular fibroadenoma of breast', 'breast intracanalicular fibroadenoma', 'intracanalicular fibroadenoma', 'intracanalicular fibroadenoma of the breast', 'intracanalicular breast fibroadenoma']",2656,,,C0334496,,C4271,,,,,,
mondo:0002378,dermoid cyst,"['dermoid cyst, benign', 'dermoid choristoma', 'dermoid tumour', 'teratoma, benign', 'dermoid tumor', 'teratoma, benign (morphologic abnormality)', 'benign cystic teratoma', 'mature cystic teratoma', 'dermoid', 'subcutaneous cystic teratoma', 'cystic dermoid choristoma', 'dermoid cyst']",2658,,,C2700593,,C9011,1000894,D003884,,,,
mondo:0002379,cystic teratoma,['cystic teratoma'],2660,,,C1368903,,C9014,,,,,,
mondo:0002380,myoepithelial tumor,"['myoepithelioma', 'myoepithelial tumor', 'benign myoepithelioma', 'myoepithelial adenoma', 'myoepithelial neoplasm']",2661,,,C1947949,,C40392,,D009208,,,,
mondo:0002381,sweat gland neoplasm,"['sweat gland tumour', 'tumor of sweat gland', 'sweat gland neoplasm (disease)', 'tumour of the sweat gland', 'neoplasm of sweat gland', 'sweat gland tumor', 'sweat gland neoplasm', 'sweat gland tumor (morphologic abnormality)', 'tumour of sweat gland', 'sweat gland tumour (morphologic abnormality)', 'sweat gland tumour NOS (morphologic abnormality)', 'neoplasm of the sweat gland', 'tumor of the sweat gland', 'sweat gland tumor NOS (morphologic abnormality)', 'sweat gland neoplasms']",2664,,,C0038987,,C3398,1001204,D013544,239.2,,,
mondo:0002382,benign mesenchymoma,"['mesenchymoma, benign', 'mesenchymal tumor, benign', 'mesenchymoma, benign (morphologic abnormality)']",2667,,,C0334491,,C4267,,,,,,
mondo:0002383,Pacinian tumor,"['Pacinian tumour (morphologic abnormality)', 'Pacinian neurofibroma', 'Pacinian tumor (morphologic abnormality)']",2669,,,C0334599,,C4328,,,215.9,,,
mondo:0002385,benign cystic nephroma,"['benign multilocular cystic nephroma', 'benign cystic nephroma', 'cystic nephroma']",2673,,,C1266138,,C7504,1000213,,,,,
mondo:0002386,mixed epithelial stromal tumor of the kidney,"['MEST', 'mixed epithelial and stromal tumour of kidney', 'mixed epithelial stromal tumor of the kidney', 'benign MEST', 'mixed epithelial and stromal tumor of kidney', 'adult mesoblastic nephroma']",2678,,,C1272677,,C37263,1000381,,,,,
mondo:0002387,liver angiosarcoma,"['hemangiosarcoma of the liver', 'Lias', 'primary angiosarcoma of liver', 'hepatic angiosarcoma', 'liver angiosarcoma (disease)', 'primary angiosarcoma of the liver', 'liver hemangiosarcoma', 'liver angiosarcoma', 'hepatic hemangiosarcoma', 'angiosarcoma of the liver', 'angiosarcoma of liver', 'hemangiosarcoma of liver']",268,,,C0345907,,C4438,,,,C22.3,,
mondo:0002388,intracystic papillary adenoma,"['intracystic papillary adenoma', 'intracystic papilloma', 'intracystic papillary adenoma (morphologic abnormality)']",2682,,,C0334374,,C4191,,,,,,
mondo:0002395,renal adenoma,"['adenoma, renal cell, benign', 'renal cell adenoma (morphologic abnormality)', 'renal tubule adenoma', 'renal cell adenoma', 'kidney adenoma', 'renal adenoma']",2697,,,C0334684,,C8383,,,,,,
mondo:0002396,nephrogenic adenofibroma,['metanephric adenofibroma'],2698,,,C1266141,,C39812,,,,,,
mondo:0002397,liver sarcoma,"['sarcoma of the liver', 'sarcoma of liver', 'hepatic sarcoma', 'liver sarcoma']",270,,,C0345906,,C4437,,,,,,
mondo:0002398,mucinous adenofibroma,['mucinous adenofibroma'],2700,,,C0334499,,C8978,,,,,,
mondo:0002399,"tenosynovial giant cell tumor, localized type","['localized giant cell neoplasm of Tenosynovium', 'localised giant cell tumour of the Tenosynovium', 'localised giant cell neoplasm of tendon sheath', 'localized giant cell neoplasm of the Tenosynovium', 'benign synovioma', 'localised giant cell tumour of tendon sheath', 'localized tenosynovial giant cell neoplasm', 'localised giant cell tumour of Tenosynovium', 'localized giant cell tumor of tendon sheath', 'benign tumor of synovium', 'localised tenosynovial giant cell neoplasm', 'localised giant cell neoplasm of Tenosynovium', 'synovioma, benign (morphologic abnormality)', 'benign tumour of synovium', 'localized giant cell tumor of Tenosynovium', 'localized tenosynovial giant cell tumor', 'localized giant cell tumor of the Tenosynovium', 'localised tenosynovial giant cell tumour', 'nodular tenosynovitis', 'localized giant cell neoplasm of tendon sheath', 'localised giant cell neoplasm of the Tenosynovium', 'tenosynovial giant cell tumor, localized type']",2701,,,C0588125,,C6532,,,727.02,,,
mondo:0002400,synovitis,"['synovitis', 'synovial membrane of synovial joint inflammation', 'Synovitides', 'synovitis (disease)']",2703,,,,,C50766,0008997,D013585,,,,0100769
mondo:0002401,malignant tenosynovial giant cell tumor,"['malignant giant cell neoplasm of tendon sheath', 'tenosynovial giant cell tumor, malignant', 'malignant giant cell tumor of the tendon sheath', 'malignant giant cell tumour of tendon sheath', 'malignant tendon sheath giant cell tumor', 'malignant tendon sheath giant cell tumour', 'giant cell tumour of tendon sheath, malignant', 'malignant giant cell neoplasm of the tendon sheath', 'malignant giant cell tumour of the tendon sheath', 'giant cell tumor of tendon sheath, malignant', 'malignant tenosynovial giant cell tumor', 'malignant tendon sheath giant cell neoplasm', 'malignant giant cell tumor of tendon sheath']",2704,,,C1266168,,C6535,,,,,,
mondo:0002402,malignant giant cell tumor,"['malignant tumor, giant cell type', 'giant cell tumor, malignant', 'malignant giant cell neoplasm', 'malignant giant cell tumor', 'malignant tumor, giant cell type (morphologic abnormality)']",2705,,,C0334229,,C4090,,,,,,
mondo:0002403,synovium cancer,"['malignant neoplasm of synovium', 'malignant layer of synovial tissue neoplasm', 'malignant neoplasm of synovial membrane of synovial joint', 'malignant synovial tumour', 'cancer of synovial membrane of synovial joint', 'malignant tumor of synovium', 'malignant tumour of synovium', 'layer of synovial tissue cancer', 'malignant tumor of the synovium', 'malignant neoplasm of layer of synovial tissue', 'malignant synovial neoplasm', 'malignant tumour of the synovium', 'cancer of layer of synovial tissue', 'malignant synovial tumor', 'malignant synovial membrane of synovial joint neoplasm', 'malignant neoplasm of the synovium']",2706,,,C1334624,,C6531,,,,,,
mondo:0002404,liver hemangioma,"['liver angioma', 'liver hemangioma', 'hemangioma of the liver', 'angioma of liver', 'angioma of the liver', 'hepatic hemangioma', 'hepatic angioma', 'hemangioma of liver']",271,,,C0238246,,C3869,,,,,,
mondo:0002405,hepatic vascular disorder,"['hepatic vascular disorder', 'liver vascular disorder', 'vascular disorder of liver']",272,,,C0400923,,C35442,,,573.8,,,
mondo:0002406,dermatitis,"['inflammation of skin', 'skin inflammation', 'inflammation of the skin', 'inflammatory skin disease', 'zone of skin inflammation']",2723,,,C0011603,,C2983,1000636,D003872,692.9,,,
mondo:0002407,capillary hemangioma,"['cellular hemangioma of infancy (strawberry nevus)', 'capillary hemangioma (morphologic abnormality)', 'strawberry nevus', 'congenital vascular hamartoma', 'congenital vascular naevus', 'capillary angioma', 'capillary hemangioma', 'cellular hemangioma of infancy', 'infantile hemangioma', 'strawberry haemangioma', 'strawberry nevus of skin', 'juvenile hemangioma']",2725,,,C0206733,,C7457,,D018324,,,,
mondo:0002408,hereditary hyperbilirubinemia,"['bilirubin metabolic disorder', 'hereditary hyperbilirubinemia', 'hyperbilirubinemia', 'hyperbilirubinaemia']",2741,,,C0020435,,C84761,,D006933,,,,
mondo:0002409,auditory system disorder,"['ear and mastoid disease', 'auditory system disease', 'auditory system disease or disorder', 'disorder of auditory system', 'disease of auditory system', 'auditory disease']",2742,,,C0013447,,C26757,1001455,,388.9,H60-H95,,
mondo:0002410,pyeloureteritis cystica,,2743,,,C0156254,,,,,590.3,N28.85,,
mondo:0002411,narcissistic personality disorder,,2745,,,,,C92635,,,301.81,F60.81,,
mondo:0002412,disorder of glycogen metabolism,"['glycogen metabolism disorder', 'inborn error of glycogen metabolic process', 'glycogenosis', 'rare inborn error of glycogen metabolic process', 'GSD', 'glycogenoses', 'glycogen storage disease']",2747,,79201,C0017919,,C61272,,D006008,271.0,E74.0,10061990,
mondo:0002413,glycogen storage disease I,"['hepatorenal glycogenosis', 'GSD type 1', 'deficiency of glucose-6-phosphatase', 'glycogenosis type 1', 'GSD due to G6P deficiency', 'glycogen storage disease type 1', 'GSD type I', 'glycogen storage disease due to G6P deficiency', 'glycogen storage disease type I', 'glycogen storage disease, type I', 'glycogenosis type I', 'glycogen storage disease due to glucose-6-phosphatase deficiency', 'von Gierke^s disease', 'von Gierke disease', 'G6P deficiency', 'GSD1']",0081329,,364,,"['0.0942', '-0.284', '-0.12225', '0.077', '0.7896', '-0.3525', '-0.24', '0.4521', '-0.2156', '0.1204', '0.10547', '-0.1225', '-0.259', '0.6104', '-0.545', '0.02194', '0.1442', '-0.2864', '-0.3972', '-0.1982', '0.3696', '-0.5864', '0.6294', '-0.288', '-0.2922', '-0.209', '-0.64', '-0.639', '-0.2084', '0.093', '1.046', '0.3828', '0.508', '0.1328', '-0.256', '-0.4133', '-0.3906', '-0.1887', '-0.4343', '0.3293', '-0.584', '0.08954', '0.6694', '0.5986', '-0.4775', '0.05298', '0.2114', '0.06204', '-0.503', '0.413', '-0.1692', '-0.123', '0.7314', '-0.336', '-0.2244', '-0.2369', '0.122', '-0.01942', '-0.933', '0.1372', '0.3904', '-0.00554', '-0.00791', '-0.2203', '0.0719', '-0.2915', '0.4731', '-0.1926', '-0.572', '0.1838', '-0.3633', '-0.4556', '0.05136', '-0.1808', '0.573', '0.4927', '0.05374', '-0.3938', '-0.3567', '-0.0785', '-0.05698', '-0.1708', '-0.03717', '-0.323', '-0.2634', '0.8696', '0.7065', '-0.1553', '0.746', '-0.552', '0.2002', '0.358', '-0.64', '-0.2327', '0.228', '0.749', '0.00903', '-0.4731', '-0.0445', '0.5503']",C84733,,D005953,,E74.01,10018464,
mondo:0002414,gastric hemangioma,"['angioma of the stomach', 'angioma of stomach', 'gastric angioma', 'hemangioma of stomach', 'gastric hemangioma', 'stomach hemangioma', 'hemangioma of the stomach']",275,,,C1333770,,C5481,,,,,,
mondo:0002415,bone carcinoma,"['carcinoma of bone element', 'bone element carcinoma']",2762,,,C0700110,,C36082,,,,,,
mondo:0002416,ethmoid sinus squamous cell carcinoma,"['ethmoidal sinus epidermoid carcinoma', 'ethmoid sinus epidermoid carcinoma', 'ethmoid sinus squamous cell carcinoma', 'epidermoid carcinoma of ethmoid sinus', 'epidermoid carcinoma of ethmoidal sinus', 'epidermoid carcinoma of the ethmoidal sinus', 'squamous cell carcinoma of the ethmoidal sinus', 'epidermoid carcinoma of the ethmoid sinus', 'squamous cell carcinoma of ethmoid sinus', 'ethmoidal sinus squamous cell carcinoma', 'squamous cell carcinoma of the ethmoid sinus', 'squamous cell carcinoma of ethmoidal sinus']",2763,,,C1333477,,C6065,,,,,,
mondo:0002418,ethmoid sinus adenocarcinoma,"['adenocarcinoma of the ethmoid sinus', 'adenocarcinoma of ethmoid sinus']",2766,,,C1333472,,C6237,,,,,,
mondo:0002419,transient tic disorder,['benign Tic disorder of childhood'],2768,,,,,C116767,,,307.21,F95.0,,
mondo:0002420,tic disorder,,2769,,,,,,,D013981,307.20,,,
mondo:0002422,adamantinoma,"['Extragnathic adamantinoma', 'adamantinoma', 'adamantinoma of long bone', 'adamantinoma, malignant', 'adamantinoma of long bones', 'adamantinoma of long bones (morphologic abnormality)', 'long bone adamantinoma']",2776,102660,55881,C1367554,,C7644,,D050398,170.9,C40.2,,
mondo:0002423,rectosigmoid junction neoplasm,"['tumor of rectosigmoid junction', 'neoplasm of the rectosigmoid junction', 'tumor of the rectosigmoid junction', 'rectosigmoid junction tumour', 'tumour of rectosigmoid junction', 'rectosigmoid tumour', 'tumour of the rectosigmoid junction', 'rectosigmoid junction neoplasm (disease)', 'rectosigmoid neoplasm', 'rectosigmoid tumor', 'rectosigmoid junction tumor', 'neoplasm of rectosigmoid junction']",2780,,,C0345873,,C4877,,,,,,
mondo:0002424,rectosigmoid carcinoma,"['carcinoma of rectosigmoid junction', 'rectosigmoid cancer', 'rectosigmoid carcinoma', 'rectosigmoid junction carcinoma']",2781,,,C1327709,,C7421,,,,,,
mondo:0002425,rectosigmoid junction cancer,"['malignant rectosigmoid junction neoplasm', 'malignant rectosigmoid neoplasm', 'malignant rectosigmoid tumor', 'malignant tumour of the rectosigmoid junction', 'malignant neoplasm of rectosigmoid junction', 'malignant neoplasm of the rectosigmoid junction', 'cancer of rectosigmoid junction', 'malignant tumor of rectosigmoid junction', 'malignant rectosigmoid tumour', 'malignant tumour of rectosigmoid junction', 'malignant tumor of the rectosigmoid junction', 'malignant neoplasm of rectosigmoid', 'rectosigmoid junction cancer']",2782,,,C0153443,,C7420,,,154.0,C19,,
mondo:0002426,lung sarcoma,"['pulmonary sarcoma', 'sarcoma of the lung', 'lung sarcoma', 'sarcoma of lung']",2784,,,C0598790,,C4860,,,,,,
mondo:0002427,cerebellar disorder,"['disorder of cerebellum', 'disease of cerebellum', 'cerebellum disease or disorder', 'cerebellum disease']",2786,,,C0007760,,,,D002526,,,,
mondo:0002428,protozoa infectious disease,"['parasitic protozoa infectious disease', 'protozoal infection', 'Mastigophora infectious disease', 'sarcomastigophora infectious disease']",2789,,,,,C34953,,D011528,,B50-B64,,
mondo:0002429,idiopathic interstitial pneumonia,"['diffuse idiopathic pulmonary fibrosis', 'noninfectious pneumonia', 'idiopathic fibrosing alveolitis', 'IPF', 'idiopathic interstitial pneumonitis', 'IIp']",2797,,98300,C2350236,,C35714,,D054988,,,,
mondo:0002432,malignant neoplasm of acoustic nerve,"['malignant eighth cranial nerve tumour', 'malignant neoplasm of the vestibulocochlear nerve', 'malignant tumour of acoustic nerve', 'malignant tumor of the eighth cranial nerve', 'cancer of the vestibulocochlear nerve', 'malignant eighth cranial nerve neoplasm', 'malignant tumor of vestibulocochlear nerve', 'malignant tumour of eighth cranial nerve', 'malignant neoplasm of the eighth cranial nerve', 'malignant tumour of vestibulocochlear nerve', 'malignant tumor of acoustic vestibular nerve', 'malignant vestibulocochlear nerve neoplasm', 'malignant tumour of the acoustic nerve', 'malignant tumor of the vestibulocochlear nerve', 'malignant eighth cranial nerve tumor', 'malignant neoplasm of the acoustic nerve', 'malignant acoustic nerve tumour', 'malignant tumour of the eighth cranial nerve', 'malignant vestibulocochlear nerve tumour', 'cancer of vestibulocochlear nerve', 'malignant tumor of the acoustic nerve', 'malignant tumour of the vestibulocochlear nerve', 'malignant tumour of acoustic vestibular nerve', 'malignant acoustic nerve neoplasm', 'malignant neoplasm of eighth cranial nerve', 'malignant acoustic nerve tumor', 'vestibulocochlear nerve cancer', 'malignant vestibulocochlear nerve tumor', 'malignant tumor of acoustic nerve', 'malignant neoplasm of vestibulocochlear nerve', 'malignant tumor of eighth cranial nerve']",2814,,,C0346331,,C4539,,,,,,
mondo:0002433,malignant cranial nerve neoplasm,"['malignant neoplasm of cranial nerve', 'cancer of cranial nerve', 'malignant cranial nerve tumour', 'malignant tumour of the cranial nerve', 'malignant neoplasm of the cranial nerve', 'malignant tumour of cranial nerve', 'cranial nerve malignant neoplasm', 'malignant cranial nerve neoplasm', 'cranial nerve cancer', 'malignant tumor of the cranial nerve', 'malignant neoplasm of cranial nerves', 'cranial nerve neoplasm, malignant', 'malignant cranial nerve tumor', 'malignant tumor of cranial nerve']",2815,,,C0153644,,C3571,,,192.0,,,
mondo:0002434,oculomotor nerve cancer,"['malignant oculomotor nerve tumour', 'malignant oculomotor nerve neoplasm', 'primary malignant neoplasm of oculomotor nerve', 'malignant neoplasm of oculomotor nerve', 'IIIrd cranial nerve neoplasm, malignant', 'malignant oculomotor nerve tumor', 'oculomotor nerve cancer', 'oculomotor nerve neoplasm, malignant', 'cancer of oculomotor nerve']",2816,,,C0686417,,C6995,,,,,,
mondo:0002435,oculomotor nerve neoplasm,"['oculomotor nerve neoplasm (disease)', 'IIIrd cranial nerve tumour', 'tumor of oculomotor nerve', 'cranial nerve III tumor', 'oculomotor nerve tumour', 'cranial nerve III tumour', 'neoplasm of oculomotor nerve', 'IIIrd cranial nerve tumor', 'oculomotor nerve tumor', 'tumour of oculomotor nerve', 'oculomotor nerve neoplasm']",2817,,,C1263895,,C6994,,,239.7,,,
mondo:0002436,nasal disorder,"['nasal disorder', 'nose disease', 'disorder of the nose', 'nose disease or disorder', 'disorder of nose', 'disease of nose']",2825,,,C0028432,,,,D009668,478.19,,,
mondo:0002437,dehydration polycythemia,,2833,,,C0856815,,C27310,,,,,,
mondo:0002438,acquired polycythemia,"['polycythemia, secondary', 'acquired polycythemia', 'acquired polycythemia (disease)']",2834,,,C1318533,,C27178,,,289.0,,,
mondo:0002440,erythropoietin polycythemia,"['nephrogenous polycythemia', 'polycythemia, nephrogenous', 'polycythaemia due to Excess erythropoetin production', 'polycythemia due to excess erythopoetin production', 'secondary polycythemia with excess erythropoietin']",2839,,,C0391869,,C35434,,,,,,
mondo:0002441,Jervell and Lange-Nielsen syndrome,"['prolonged QT interval in EKG and sudden death', 'Surdo-cardiac syndrome', 'Jervell Lange-Nielsen syndrome', 'JLNS1', 'Jervell and Lange-Nielson syndrome', 'Jervell and Lange Nielsen syndrome', 'Jervell and Lange-Nielsen syndrome 1', 'long QT interval-deafness syndrome', 'deafness, congenital, and functional heart disease', 'Jervell and Lange-Nielsen syndrome type 1', 'Jervell-Lange Nielsen syndrome', 'Cardioauditory syndrome of Jervell and Lange-Nielsen']",2842,,90647,C0022387,"['-0.0848', '0.1705', '0.1542', '-0.0962', '0.274', '-0.3372', '0.08344', '0.1786', '-0.0707', '-0.2219', '0.072', '-0.01304', '0.03174', '-0.05804', '-0.1681', '-0.0802', '-0.11224', '-0.1311', '-0.1437', '-0.327', '0.0679', '-0.02716', '0.01718', '-0.003578', '0.207', '-0.0225', '-0.05264', '-0.153', '0.235', '-0.1536', '0.11255', '0.06445', '0.1221', '0.003672', '-0.1654', '-0.2386', '0.0742', '-0.0938', '-0.007324', '-0.3252', '0.02199', '-0.2195', '0.2612', '-0.0943', '-0.02411', '-0.2517', '-0.2292', '0.2073', '0.3262', '0.05634', '-0.02081', '-0.06082', '-0.05438', '-0.05545', '0.02988', '-0.3406', '0.2383', '0.263', '-0.1992', '0.0707', '0.10046', '0.009796', '0.2063', '-0.03204', '-0.0743', '-0.0776', '-0.06964', '0.0826', '-0.2986', '0.1923', '-0.4343', '-0.04663', '0.1443', '-0.0701', '0.0413', '0.2042', '0.06604', '0.1613', '-0.1842', '0.02861', '0.203', '0.1117', '-0.0398', '0.1807', '-0.0052', '0.04016', '0.182', '0.292', '-0.001628', '0.3215', '-0.05972', '0.2086', '0.0912', '0.097', '0.445', '0.1829', '0.3801', '-0.654', '-0.1052', '0.10925']",C84793,,D029593,,,10057936,
mondo:0002442,long QT syndrome,"['ventricular arrhythmia associated with long QT syndrome', 'long Q-T syndrome', 'LQT']",2843,,,C0023976,,C34786,,D008133,426.82,I45.81,,
mondo:0002443,bruxism,"['bruxism', 'bruxism (disease)', 'sleep related bruxism', 'grinding teeth', 'teeth grinding', 'bruxism - teeth grinding']",2846,,,,,,,D002012,327.53,,,0003763
mondo:0002444,melancholia,"['melancholic depression', 'depression with melancholic features']",2848,,,,,C34812,,,,,,
mondo:0002447,endometrial carcinoma,"['endometrial cancer', 'carcinoma of endometrium', 'endometrium carcinoma', 'endometrial carcinoma (disease)', 'carcinoma of the endometrium', 'endometrial carcinoma', 'carcinoma, endometrial, malignant']",2871,,,C0476089,,C7558,,,,,,0012114
mondo:0002448,laryngeal sarcoma,"['laryngeal sarcoma', 'larynx sarcoma', 'sarcoma of larynx', 'sarcoma of the larynx']",2877,,,C1334377,,C6020,,,,,,
mondo:0002449,nodular degeneration of cornea,,2879,,,C0155122,,,,,371.46,,,
mondo:0002450,prostatic adenoma,"['adenoma of the prostate', 'prostate adenoma', 'adenoma - prostate', 'benign adenoma of prostate', 'adenoma of prostate', 'prostate gland adenoma']",2883,,,C0520477,,C4795,,D011470,600.20,,,
mondo:0002451,benign prostate phyllodes tumor,"['phyllodes neoplasm of the prostate', 'benign phyllodes tumour of prostate', 'benign prostate phyllodes neoplasm', 'benign phyllodes neoplasm of the prostate', 'benign phyllodes tumor of the prostate', 'prostate phyllodes tumor, benign', 'benign prostate phyllodes tumor', 'benign phyllodes tumour of the prostate', 'prostate phyllodes tumor', 'prostate phyllodes tumour', 'benign phyllodes neoplasm of prostate', 'benign phyllodes tumor of prostate']",2885,,,C1332535,,C5532,,,,,,
mondo:0002452,prostate leiomyoma,"['leiomyoma of prostate gland', 'leiomyoma of the prostate', 'prostate gland leiomyoma', 'leiomyoma of prostate', 'prostatic leiomyoma', 'prostate leiomyoma']",2887,,,C1335510,,C5544,,,,,,
mondo:0002453,retrocochlear disease,,2889,,,C0035352,,,,D012181,,,,
mondo:0002455,exocervical carcinoma,"['exocervical carcinoma', 'ectocervix carcinoma', 'carcinoma of exocervix', 'exocervix carcinoma', 'carcinoma of ectocervix', 'carcinoma of the exocervix', 'exocervical cancer']",2892,,,C1299238,,C7453,,,,,,
mondo:0002457,Treacher-Collins syndrome,"['Franceschetti syndrome', 'Franceschetti-Klein syndrome', 'TCOF', 'mandibulofacial dysostosis without limb anomalies', 'MFD1', 'Treacher Collins syndrome', 'TCS']",2908,,861,C0265241,"['0.28', '-0.001234', '0.1381', '-0.7544', '0.3044', '0.424', '0.7856', '1.324', '-1.3955', '-0.526', '-0.2134', '-0.5034', '-0.503', '0.1692', '-0.3052', '-0.03094', '0.45', '-0.4563', '-0.597', '-0.02573', '-0.5317', '-0.2122', '0.10974', '-0.5493', '0.399', '0.315', '-0.6846', '0.338', '0.4575', '-0.0446', '-0.1863', '0.365', '-0.06854', '-0.1394', '-0.3394', '-0.362', '0.008934', '-0.1542', '-0.3267', '-0.323', '0.3362', '0.1433', '0.2693', '-0.518', '-0.2391', '-0.4148', '-0.1808', '-0.05383', '0.2343', '0.386', '-0.2252', '-0.2766', '-0.01799', '0.1384', '-0.2654', '-0.2166', '0.1587', '0.0476', '0.05768', '-0.06635', '0.1846', '0.4941', '-0.5967', '0.0723', '-0.4338', '-0.172', '0.396', '-0.01057', '0.09717', '0.4656', '0.0671', '0.06573', '0.4353', '0.02025', '0.5024', '-0.10614', '0.1985', '-0.1755', '-0.7515', '-0.3223', '-0.4011', '-0.3513', '0.7354', '1.008', '-0.3162', '0.3186', '0.07904', '0.708', '0.165', '0.12115', '-0.7344', '0.7188', '0.02661', '0.0729', '0.933', '-0.4595', '0.6787', '-0.8853', '0.357', '0.4404']",C75018,,,,,10051456,
mondo:0002459,type IV hypersensitivity disease,"['type 4 hypersensitivity reaction', 'type IV hypersensitivity reaction', 'delayed-type hypersensitivity response', 'delayed hypersensitivity reaction', 'immunoproliferative disease', 'disorder of type IV hypersensitivity', 'DTH', 'delayed-type hypersensitivity', 'type IV hypersensitivity', 'hypersensitivity reaction type IV disease']",2916,,,C0020522,,C3115,,,,,,
mondo:0002460,lacrimal system cancer,"['malignant neoplasm of lacrimal apparatus', 'lacrimal system neoplasm', 'lacrimal system tumor', 'tumour of the lacrimal system', 'neoplasm of lacrimal system', 'malignant lacrimal apparatus neoplasm', 'tumor of the lacrimal system', 'cancer of lacrimal apparatus', 'lacrimal system tumour', 'tumour of lacrimal system', 'neoplasm of the lacrimal system', 'tumor of lacrimal system', 'lacrimal system neoplasms']",292,,,C1334361,,C5102,,,,,,
mondo:0002461,membranoproliferative glomerulonephritis,"['chronic glomerulonephritis, lobular', 'membranoproliferative glomerulonephritis (disease)', 'membranoproliferative glomerulonephritis', 'lobular glomerulonephritis']",2920,,,C0017662,,C34644,,D015432,,,,0000793
mondo:0002462,glomerulonephritis,"['bright^s disease', 'nephritis of renal glomerulus', 'glomerulonephritis', 'glomerulonephritis (disease)', 'renal glomerulus nephritis', 'glomerular nephritis']",2921,,,C0017658,,C26784,,D005921,583.9,,,0000099
mondo:0002463,lacrimal gland carcinoma,"['lacrimal gland carcinoma', 'carcinoma of the lacrimal gland', 'carcinoma of lacrimal gland']",293,,,C1334358,,C6129,,,,,,
mondo:0002464,lacrimal gland cancer,"['malignant neoplasm of lacrimal gland', 'tumor of the lacrimal gland', 'malignant tumour of lacrimal gland', 'malignant tumour of the lacrimal gland', 'cancer of lacrimal gland', 'malignant lacrimal gland tumor', 'malignant lacrimal gland tumour', 'lacrimal gland cancer', 'malignant tumor of the lacrimal gland', 'malignant tumor of lacrimal gland', 'malignant lacrimal gland neoplasm', 'tumour of the lacrimal gland', 'malignant neoplasm of the lacrimal gland']",294,,,,,C3563,,,239.89,,,
mondo:0002465,bronchiolitis,"['wheezy bronchitis', 'bronchiolitis', 'bronchiolitis (disease)', 'RSV bronchiolitis', 'viral bronchiolitis']",2942,,,C0006271,,C39658,,D001988,466.19,,,0011950
mondo:0002466,eye carcinoma,"['ocular carcinoma', 'carcinoma of the eye', 'eye carcinoma', 'carcinoma of eyeball of camera-type eye', 'carcinoma of eye']",295,,,C0848866,,C6079,,,,,,
mondo:0002467,inner ear disorder,"['disorder of internal ear', 'labyrinthine disease', 'inner Ear disorder', 'disease of internal ear', 'vestibular disorder', 'internal ear disease or disorder', 'internal ear disease', 'internal Ear disorder']",2952,,,,,C27166,,D007759,,H80-H83,,
mondo:0002468,hyperimmunoglobulin syndrome,['hyperimmunoglobulin syndrome'],2959,,,C1334069,,C27579,,,,,,
mondo:0002469,lacrimal gland carcinoma ex pleomorphic adenoma,"['lacrimal gland carcinoma ex pleomorphic adenoma', 'lacrimal gland malignant mixed tumour', 'malignant mixed tumor of the lacrimal gland', 'malignant mixed tumour of the lacrimal gland', 'malignant mixed tumor of lacrimal gland', 'mixed lacrimal gland cancer', 'malignant mixed neoplasm of the lacrimal gland', 'lacrimal gland malignant mixed tumor', 'malignant mixed tumour of lacrimal gland', 'carcinoma ex pleomorphic adenoma of lacrimal gland', 'carcinoma ex pleomorphic adenoma of the lacrimal gland', 'carcinoma Ex pleomorphic adenoma of the lacrimal gland', 'lacrimal gland malignant mixed neoplasm', 'malignant mixed neoplasm of lacrimal gland']",296,,,C0346342,,C6804,,,,,,
mondo:0002470,photosensitive trichothiodystrophy,"['Tay syndrome', 'trichothiodystrophy', 'IBIDS syndrome', 'Ichtyosis, brittle hair, intellectual impairment, decreased fertility, and short stature', 'trichothiodystrophy with congenital ichthyosis', 'sulfur-deficient brittle hair syndrome', 'trichothiodystrophy with congenital ichtyosis']",2960,,453,CN205101,,C4924,,,,,,
mondo:0002471,bursitis,"['synovial bursa inflammation', 'Capsulitides', 'adhesive Capsulitides, shoulder', 'Capsulitides, adhesive', 'shoulder, frozen', 'Bursitides', 'frozen shoulder', 'capsulitis, shoulder adhesive', 'capsulitis', 'adhesive capsulitis, shoulder', 'shoulders, frozen', 'Capsulitides, shoulder adhesive', 'capsulitis, adhesive', 'adhesive capsulitis', 'adhesive Capsulitides', 'shoulder adhesive capsulitis', 'frozen shoulders', 'adhesive capsulitis of the shoulder', 'shoulder adhesive Capsulitides']",2965,,,C0006444,,C94407,,D002062,727.3,,,
mondo:0002472,carcinoma ex pleomorphic adenoma,"['carcinoma in pleomorphic adenoma', 'carcinoma ex pleomorphic adenoma', 'carcinoma ex pleomorphic adenoma (morphologic abnormality)']",,,,C0344460,,C4397,,,,,,
mondo:0002473,cystic kidney disease,"['renal cyst', 'kidney cyst', 'cystic renal disease']",2975,,,C0022679,,C34750,,D052177,,Q61,,
mondo:0002474,primary hyperoxaluria,"['hyperoxaluria, primary', 'primary hyperoxaluria']",2977,,416,C0020501,"['-0.00417', '0.21', '-0.5366', '0.4402', '-0.0916', '0.01582', '-0.2484', '1.125', '-0.4568', '0.359', '-0.1422', '0.08545', '-0.36', '0.11536', '-0.307', '-0.4214', '0.2067', '-0.2969', '0.01869', '0.0608', '-0.256', '-0.2169', '0.7686', '-0.6826', '0.3984', '0.1217', '-0.1151', '-0.421', '-0.591', '0.05243', '0.6733', '-0.411', '0.0698', '-0.2688', '-0.0682', '-0.9727', '-0.4314', '-0.5757', '0.07294', '-0.06934', '-0.04028', '-0.4001', '0.636', '-0.7173', '-0.1351', '0.004704', '0.2612', '-0.03894', '-0.3955', '0.948', '0.2263', '0.4316', '0.6445', '-0.09576', '-0.1521', '-0.3115', '0.707', '0.3062', '-0.602', '0.3877', '0.5386', '-0.1832', '0.0982', '-0.5625', '-0.0537', '0.0652', '0.326', '0.3013', '-0.614', '-0.388', '0.3816', '-0.252', '0.3718', '-0.05087', '0.4844', '0.2386', '0.2256', '-0.438', '-0.3118', '0.02634', '-0.5693', '-0.2788', '0.11554', '0.2522', '0.461', '-0.3328', '0.1886', '-0.5464', '0.06555', '0.1987', '0.4348', '0.322', '-0.8384', '-0.2107', '0.4863', '0.2646', '0.6016', '-0.5835', '-0.4326', '0.01054']",C123158,,D006960,271.8,,10020703,
mondo:0002475,lacrimal gland adenocarcinoma,"['lacrimal gland adenocarcinoma', 'adenocarcinoma of the lacrimal gland', 'adenocarcinoma of lacrimal gland']",298,,,C0346341,,C4541,,,,,,
mondo:0002476,anuria,['suppression of urinary secretion'],2983,,,C0003460,,,,D001002,,,,
mondo:0002477,prostate neuroendocrine neoplasm,"['prostate gland neuroendocrine tumour', 'neuroendocrine tumor of the prostate', 'prostate gland neuroendocrine neoplasm', 'prostate neuroendocrine carcinoma', 'neuroendocrine neoplasm of the prostate', 'neuroendocrine neoplasm of prostate gland', 'prostate gland NET', 'prostate neuroendocrine neoplasm', 'neuroendocrine tumour of the prostate', 'prostate gland neuroendocrine tumor', 'prostate gland neuroendocrine tumor, well differentiated, low or intermediate grade', 'neuroendocrine neoplasm of prostate']",2992,,,C1335515,,C5545,,,,,,
mondo:0002478,mixed germ cell-sex cord-stromal tumor,"['mixed germ cell-Sex cord-stromal tumor', 'mixed germ cell-sex cord-stromal tumor (morphologic abnormality)', 'mixed germ cell-sex cord-stromal tumour (morphologic abnormality)', 'mixed germ cell-Sex cord tumor', 'mixed germ cell-Sex cord-stromal tumour', 'mixed germ cell-Sex cord-stromal neoplasm', 'mixed germ cell-Sex cord neoplasm', 'mixed germ cell-Sex cord tumour']",2996,,,C1321220,,C5241,,,,,,
mondo:0002479,Sertoli-Leydig cell tumor,,2997,,,C0206723,,,,D018310,,,,
mondo:0002480,endometrioid tumor,"['female reproductive endometrioid tumor', 'endometrioid neoplasm', 'endometrioid tumor of the female reproductive system', 'endometrioid tumor', 'endometrioid tumour (morphologic abnormality)', 'endometrioid tumour of female reproductive system', 'female reproductive endometrioid cancer', 'endometrioid tumor of female reproductive system', 'female reproductive endometrioid neoplasm', 'endometrioid tumour of the female reproductive system', 'endometrioid tumor (morphologic abnormality)', 'endometrioid neoplasm of female reproductive system', 'female reproductive endometrioid tumour', 'endometrioid neoplasm of the female reproductive system']",3001,,,C0474809,,C7113,0009118,,,,,
mondo:0002481,ovarian neuroendocrine neoplasm,"['neuroendocrine neoplasm of ovary', 'ovary NET', 'ovarian neuroendocrine neoplasm', 'neuroendocrine tumor of ovary', 'neuroendocrine tumour of ovary', 'ovary neuroendocrine tumor, well differentiated, low or intermediate grade', 'ovary neuroendocrine tumor', 'neuroendocrine neoplasm of the ovary', 'ovary neuroendocrine neoplasm', 'ovary neuroendocrine tumour']",3002,,,C1335172,,C5237,,,,,,
mondo:0002482,nipple neoplasm,"['tumor of the nipple', 'neoplasm of nipple', 'nipple neoplasm', 'tumor of nipple', 'neoplasm of the nipple', 'nipple tumour', 'tumour of the nipple', 'nipple neoplasm (disease)', 'nipple tumor', 'tumour of nipple']",3003,,,C1112166,,C5212,,,,,,
mondo:0002483,breast myoepithelial tumor,"['breast myoepithelial tumor', 'breast myoepithelial neoplasm']",3004,,,C1511319,,C40389,,,,,,
mondo:0002485,breast neuroendocrine neoplasm,"['breast neuroendocrine tumour', 'neuroendocrine tumor of the breast', 'breast endocrine neoplasm', 'breast NET', 'neuroendocrine tumour of the breast', 'breast neuroendocrine tumor, well differentiated, low or intermediate grade', 'neuroendocrine neoplasm of the breast', 'neuroendocrine neoplasm of breast', 'breast neuroendocrine neoplasm', 'breast neuroendocrine tumor']",3009,,,C1332635,,C5169,,,,,,
mondo:0002486,lobular neoplasia,"['lobular neoplasia', 'LIN', 'lobular intraepithelial neoplasia', 'LN']",3010,,,C0861352,,C27939,,,,,,
mondo:0002487,breast granular cell tumor,"['granular cell tumor of breast', 'breast granular cell tumor', 'granular cell tumour of breast']",3011,,,C1511312,,C40400,,,,,,
mondo:0002488,intraductal breast neoplasm,['intraductal breast neoplasm'],3013,,,C0948967,,C36083,,,,,,
mondo:0002489,malignant breast phyllodes tumor,"['malignant phyllodes tumor of breast', 'malignant phyllodes tumour of breast', 'malignant mammary phyllodes tumour', 'breast malignant phyllodes tumor', 'breast phyllodes tumor, malignant', 'malignant phyllodes tumour (morphologic abnormality)', 'breast malignant phyllodes tumour', 'malignant phyllodes tumour', 'malignant phyllodes tumour of the breast', 'malignant cystosarcoma phyllodes (morphologic abnormality)', 'malignant phyllodes neoplasm of breast', 'malignant phyllodes breast neoplasm', 'malignant phyllodes neoplasm', 'malignant cystosarcoma phyllodes of breast', 'malignant breast phyllodes tumor', 'malignant phyllodes neoplasm of the breast', 'phyllodes breast tumour', 'malignant cystosarcoma phyllodes', 'phyllodes breast tumor', 'phyllodes breast neoplasm', 'malignant phyllodes tumor of the breast', 'malignant mammary phyllodes tumor', 'malignant mammary phyllodes neoplasm', 'malignant breast phyllodes neoplasm', 'malignant phyllodes tumor (morphologic abnormality)', 'malignant cystosarcoma phyllodes of the breast', 'phyllodes tumor, malignant (morphologic abnormality)']",3016,,,,,C4504,0008545,,,,,
mondo:0002490,breast sarcoma,"['breast sarcoma', 'sarcoma of breast', 'sarcoma of the breast', 'PBS']",3017,,,C0349667,,C4670,,,,,,
mondo:0002491,substance abuse,,302,,,,,,,,305.90,,,
mondo:0002492,acute kidney failure,"['ARF', 'acute renal failure', 'AKI', 'kidney failure, acute', 'acute kidney injury']",3021,,,,,C26808,,D058186,,N17,,
mondo:0002493,prostatic acinar adenocarcinoma,"['prostatic acinar adenocarcinoma', 'acinar prostate adenocarcinoma', 'prostate acinar adenocarcinoma', 'acinar adenocarcinoma of the prostate', 'acinar adenocarcinoma of prostate']",3024,,,C1332139,,C5596,,,,,,
mondo:0002494,substance-related disorder,"['substance induced mood disorders', 'substance-related disorder']",303,,,,,C92203,,D019966,,F10-F19,,
mondo:0002495,colon signet ring cell adenocarcinoma,"['colonic signet Ring cell adenocarcinoma', 'signet Ring cell adenocarcinoma of colon', 'signet Ring cell colon adenocarcinoma', 'colon signet ring adenocarcinoma', 'colonic signet Ring adenocarcinoma', 'signet Ring cell adenocarcinoma of the colon', 'colon signet Ring cell adenocarcinoma']",3033,,,C1707436,,C7967,,,,,,
mondo:0002496,submucosal invasive colon adenocarcinoma,['submucosal invasive colon adenocarcinoma'],3038,,,C1515024,,C38760,,,,,,
mondo:0002501,brain glioblastoma,"['grade IV astrocytic neoplasm of brain', 'grade IV astrocytic tumour of the brain', 'grade IV brain astrocytic tumor', 'grade IV astrocytic tumor of brain', 'brain glioblastoma multiforme (disease)', 'brain glioblastoma (disease)', 'grade IV astrocytic tumour of brain', 'glioblastoma multiforme of brain', 'brain glioblastoma multiforme', 'grade IV brain astrocytic tumour', 'brain glioblastoma', 'grade IV astrocytic tumor of the brain', 'grade IV astrocytic neoplasm of the brain', 'glioblastoma multiforme of the brain', 'grade IV brain astrocytic neoplasm']",3073,,,C0349543,,C4642,0006545,,,,,
mondo:0002503,adult astrocytic tumor,"['astrocytic tumour', 'astrocytic tumor', 'adult astrocytoma', 'adult astrocytic neoplasm', 'adult astrocytic tumor']",3076,,,C1332183,,C7049,,,,,,
mondo:0002505,childhood astrocytic tumor,"['astrocytic tumour', 'astrocytic tumour of childhood', 'pediatric astrocytic tumor', 'astrocytic tumor', 'childhood astrocytic tumor', 'paediatric astrocytic neoplasm', 'pediatric astrocytic neoplasm', 'astrocytic tumors, childhood', 'astrocytic tumor of childhood', 'paediatric astrocytic tumour', 'paediatric astrocytoma', 'pediatric astrocytoma', 'childhood astrocytic neoplasm', 'juvenile astrocytoma (morphologic abnormality)', 'juvenile astrocytoma']",3079,,,C1321865,,C9022,,,,,,
mondo:0002507,gingival overgrowth,['gingival enlargement'],3086,,,,,,,D019214,523.8,,,
mondo:0002508,gingivitis,"['acute gingivitis', 'gingiva inflammation', 'chronic gingivitis', 'gingivitis']",3087,,,C0017574,,C34636,,D005891,523.10,,,
mondo:0002509,non-specific granulomatous orchitis,['granulomatous orchitis'],3089,,,C0436545,,C27162,,,,,,
mondo:0002511,stenosis of lacrimal sac,,3096,,,,,,,,375.54,,,
mondo:0002512,papillary adenocarcinoma,"['papillary adenocarcinoma', 'infiltrating and papillary adenocarcinoma', 'adenocarcinoma, papillary, malignant', 'infiltrating papillary adenocarcinoma', 'papillary adenocarcinoma NOS (morphologic abnormality)', 'papillary adenocarcinoma (morphologic abnormality)']",3112,,,C1321863,,C2853,,D000231,,,,
mondo:0002513,kidney benign neoplasm,"['renal and ureteral tumour', 'benign tumor of kidney', 'benign renal tumor', 'kidney benign neoplasm', 'benign tumour of kidney', 'benign renal neoplasm', 'benign neoplasm of kidney', 'benign kidney tumour', 'renal and ureteral tumor', 'renal tumor, benign', 'benign kidney tumor', 'benign kidney neoplasm', 'renal neoplasm, benign', 'benign tumor of the kidney', 'benign tumour of the kidney', 'benign renal tumour', 'benign neoplasm of the kidney']",3116,,,,,C4778,1000111,,223.0,,,
mondo:0002514,hepatobiliary neoplasm,"['liver and biliary system neoplasm', 'hepatic and biliary tumors', 'tumour of hepatobiliary system', 'hepatic and biliary tumours', 'hepato-biliary tumour', 'neoplasm of hepatobiliary system', 'liver and biliary neoplasm', 'hepatobiliary tumor', 'hepatobiliary neoplasm', 'hepato-biliary neoplasm', 'hepatic, biliary, and gallbladder neoplasms', 'hepatobiliary tumours', 'tumor of hepatobiliary system', 'hepatobiliary system neoplasm (disease)', 'hepatobiliary benign neoplasm', 'hepatobiliary tumors', 'hepatobiliary system tumor', 'hepatic and biliary neoplasms', 'hepatobiliary tumour', 'hepato-biliary tumor', 'hepatobiliary system tumour']",3117,,,C0854196,,C8614,0008550,,,,,
mondo:0002515,hepatobiliary disorder,"['liver and biliary disease', 'liver and biliary tract disease', 'hepatobiliary disorder', 'disorder of hepatobiliary system', 'hepatobiliary system disease', 'liver and biliary system disorder', 'disease of hepatobiliary system', 'liver and biliary disorder', 'hepatobiliary system disease or disorder']",3118,,,C0267792,,C3959,,,,,,
mondo:0002516,digestive system cancer,"['gastrointestinal tract cancer', 'GI tumor', 'malignant digestive system neoplasm', 'cancer of digestive system', 'malignant neoplasm of digestive system', 'GI tumour', 'digestive system cancer', 'malignant gastrointestinal neoplasm', 'malignant gastrointestinal system neoplasm', 'gastrointestinal system cancer']",3119,,,,,C4890,,,239.0,C15-C26,,
mondo:0002517,tenosynovitis of foot and ankle,,312,,,,,,,,727.06,,,
mondo:0002518,gallbladder papillary neoplasm,"['gallbladder papillomatosis', 'intracystic papillary neoplasm', 'gallbladder papillary neoplasm', 'gall bladder papillary epithelial neoplasm']",3120,,,C1333754,,C7130,,,,,,
mondo:0002519,anus disorder,"['Ulcer of anus', 'nontraumatic tear of anus', 'anal ulcer', 'disorder of anus', 'anus disease or disorder', 'anal fissure and fistula', 'anal disease', 'fissure in ano', 'anus disease', 'anal fissure', 'solitary anal ulcer', 'anal disorder', 'disease of anus']",3128,,,C1301262,,C26695,,D001004,,,,
mondo:0002520,hepatic porphyria,"['liver porphyria', 'hepatic Porphyrias', 'porphyria, hepatic', 'ALAD deficiency', 'acute hepatic porphyria', 'porphyria of liver', 'porphobilinogen synthase deficiency', 'acute porphyria', 'hepatic porphyria', 'Delta-aminolevulinate dehydratase deficiency']",3133,,95157,CN552491,,,,D017094,,,,
mondo:0002522,tenosynovial giant cell tumor,"['giant cell tumour of Tenosynovium', 'tenosynovial giant cell neoplasm', 'giant cell tumour of tendon sheath', 'giant cell tumor of Tenosynovium', 'giant cell neoplasm of Tenosynovium', 'fibrous histiocytoma of tendon sheath', 'giant cell tumor of the Tenosynovium', 'giant cell tumour of the Tenosynovium', 'tendon sheath giant cell tumour', 'tendon sheath giant cell tumor', 'giant cell neoplasm of the Tenosynovium', 'tenosynovial giant cell tumor', 'giant cell neoplasm of tendon sheath', 'tendon sheath giant cell neoplasm', 'giant cell tumor of tendon sheath']",314,,,C1318543,,C3402,1000562,,727.89,,,
mondo:0002523,cutaneous mucinosis,"['mucinosis', 'mucinoses']",3141,,,C0162855,,,,D017520,701.8,,,
mondo:0002525,inherited lipid metabolism disorder,"['dyslipidaemia', 'disorder of lipid metabolism', 'dyslipidemia', 'fatty acid metabolism disorder', 'lipid metabolism disorder']",3146,,309005,C0154251,,C97092,,,272.9,,10061227,
mondo:0002526,dermal unilateral segmental cavernous angioma,"['unilateral segmental cavernous hemangioma', 'unilateral segmental cavernous hemangioma of the skin']",3148,,,C0474966,,,,,,,,
mondo:0002527,keratoacanthoma,,3149,,,C0022572,,C3146,,D007636,,,,
mondo:0002528,synovium neoplasm,"['neoplasm of synovium', 'neoplasm of the synovium', 'tumor of the synovium', 'tumour of the synovium', 'synovial tumour', 'tumor of synovial membrane of synovial joint', 'synovial tumor', 'synovial neoplasm', 'tumor of synovium', 'synovial membrane of synovial joint neoplasm (disease)', 'synovial membrane of synovial joint tumor', 'synovial membrane of synovial joint tumour', 'synovial neoplasm NOS (morphologic abnormality)', 'neoplasm of synovial membrane of synovial joint', 'tumour of synovial membrane of synovial joint', 'synovial neoplasm (morphologic abnormality)', 'tumour of synovium']",315,,,C0476203,,C8964,,,,,,
mondo:0002529,skin squamous cell carcinoma,"['skin squamous cell carcinoma', 'cutaneous squamous cell carcinoma', 'squamous cell carcinoma - skin', 'squamous cell carcinoma of skin', 'squamous cell carcinoma of the skin', 'epidermoid carcinoma of the skin', 'epidermoid skin carcinoma', 'zone of skin squamous cell carcinoma', 'epidermoid carcinoma of skin', 'skin squamous cell cancer', 'squamous cell skin carcinoma', 'CSCC']",3151,,,C0553723,,C4819,1001927,,,,,
mondo:0002531,skin neoplasm,"['tumor of zone of skin', 'tumour of zone of skin', 'tumour of skin', 'zone of skin tumor', 'skin benign neoplasm', 'neoplasm of the skin', 'zone of skin neoplasm (disease)', 'skin tumour', 'tumour of the skin', 'zone of skin tumour', 'neoplasm of skin by site', 'tumor of the skin', 'skin neoplasms', 'neoplasm of skin', 'skin', 'skin neoplasm', 'skin tumor', 'tumor of skin', 'neoplasm of zone of skin']",3165,,,C0037286,,C3372,0004198,D012878,239.2,,,
mondo:0002532,squamous cell neoplasm,"['epidermoid cell neoplasm', 'squamous cell neoplasm', 'squamous cell tumor', 'squamous cell tumour (qualifier value)', 'epidermoid cell tumour', 'squamous cell tumor (qualifier value)', 'squamous cell tumour', 'epidermoid cell tumor']",3168,,,C0206720,,C3792,,D018307,,,,
mondo:0002533,papillary adenoma,"['papillary adenoma', 'glandular papilloma', 'adenoma, papillary, benign', 'papillary adenoma NOS (morphologic abnormality)']",3172,,,C0205650,,C79951,,,,,,
mondo:0002534,fallopian tube papilloma,"['fallopian tube papilloma', 'fallopian tube serous papilloma']",3173,,,C1517123,,C40112,,,,,,
mondo:0002535,verrucous papilloma,,3177,,,C0334243,,C4101,,,,,,
mondo:0002536,skin papilloma,"['cutaneous papilloma', 'skin papilloma', 'zone of skin papilloma', 'papilloma of skin', 'basosquamous tumor, benign', 'papilloma of the skin']",3178,,,C0347390,,C4614,,,,,,
mondo:0002537,inverted papilloma,"['inverted papilloma', 'inverted papilloma, squamous cell']",3179,,,C0206721,,C3793,,D018308,212.0,,,
mondo:0002540,childhood oligodendroglioma,"['pediatric oligodendroglioma', 'oligodendroglioma', 'paediatric oligodendroglioma', 'oligodendroglioma of childhood']",3183,,,C0280475,,C4045,,,,,,
mondo:0002541,spinal cord oligodendroglioma,"['well differentiated spinal cord oligodendroglioma', 'oligodendroglioma of spinal cord', 'spinal cord oligodendroglioma', 'well differentiated spinal cord oligodendroglial tumour', 'well differentiated spinal cord oligodendroglial tumor']",3184,,,C0346295,,C4535,,,,,,
mondo:0002542,spinal cord glioma,"['glioma of spinal cord', 'spinal cord glial neoplasm', 'spinal cord glial tumor', 'malignant glioma of spinal cord', 'glial tumor of spinal cord', 'spinal cord glioma', 'spinal cord glial tumour', 'spinal cord malignant glioma', 'glial tumour of spinal cord', 'glial neoplasm spinal cord']",3185,,,C2937245,,C4534,,,,,,
mondo:0002543,adult oligodendroglioma,"['grade II adult oligodendroglial tumour', 'adult brain oligodendroglioma', 'adult oligodendroglioma', 'grade II adult oligodendroglial tumor', 'oligodendroglioma of adults', 'oligodendroglioma']",3186,,,C0279070,,C4014,,,,,,
mondo:0002544,brain oligodendroglioma,"['brain oligodendroglioma', 'oligodendroglioma of brain', 'oligodendroglioma of the brain']",3187,,,C0346286,,C9377,,,,,,
mondo:0002545,spinal cord disorder,"['disease of the spinal cord', 'spinal cord disease', 'myelopathy', 'spinal cord disease or disorder', 'spinal cord disorder', 'disorder of spinal cord', 'disease of spinal cord']",319,,,C0037928,,C97110,,D013118,336.9,,,
mondo:0002546,schwannoma,"['schwannoma, benign', 'SCHW', 'neurolemmoma', 'benign neurilemmoma', 'neurinoma', 'benign schwannoma', 'schwannoma (WHO grade I)', 'schwannoma', 'psammomatous schwannoma', 'neurilemmoma', 'peripheral fibroblastoma']",955,,252164,CN202001,"['-0.367', '0.2369', '0.1793', '-0.11676', '0.03424', '-0.0923', '0.265', '0.0671', '-0.005306', '-0.004513', '-0.0644', '0.1205', '-0.235', '0.1953', '0.2104', '-0.03186', '-0.1263', '-0.545', '0.2852', '-0.4482', '0.05002', '-0.498', '0.2925', '-0.2864', '-0.1083', '-0.183', '-0.4048', '-0.173', '-0.1995', '0.0159', '0.1672', '-0.006584', '-0.0922', '-0.5225', '-0.0956', '-0.2045', '0.04065', '-0.0941', '0.362', '-0.3643', '-0.1659', '-0.2993', '0.0285', '-0.1234', '0.4412', '0.1387', '-0.208', '-0.0469', '0.304', '-0.05072', '0.4253', '0.2952', '0.003332', '0.2588', '-0.2922', '0.11755', '0.332', '0.05573', '-0.409', '0.4365', '0.02554', '-0.0753', '0.0996', '0.386', '-0.563', '0.2776', '0.2234', '0.98', '-0.1711', '0.751', '0.06046', '0.2137', '0.448', '0.06506', '0.1971', '0.2788', '-0.1697', '0.4211', '0.03088', '-0.8687', '-0.7573', '-0.2402', '0.3057', '0.2756', '-0.578', '-0.369', '0.1174', '-0.01901', '0.3413', '-0.1094', '0.2524', '0.0691', '-0.07294', '0.1633', '0.835', '0.06824', '0.1771', '-0.304', '0.4849', '-0.11536']",C3269,0000693,,215.9,,10029235,
mondo:0002547,nerve sheath neoplasm,"['tumour of nerve sheath', 'neoplasm of nerve sheath', 'nerve sheath tumor', 'nerve sheath tumour', 'nerve sheath neoplasm', 'neoplasm of the nerve sheath', 'tumor of nerve sheath']",3193,,,,,C4972,,D018317,,,,
mondo:0002548,cellular schwannoma,"['cellular neurinoma', 'cellular schwannoma', 'cellular neurilemmoma', 'CSCHW']",3196,,,C0431124,,C4724,,,215.9,,,
mondo:0002549,schwannoma of twelfth cranial nerve,"['schwannoma of twelfth cranial nerve', 'neurilemmoma of the hypoglossal nerve', 'hypoglossal nerve schwannoma', 'twelfth cranial nerve neurilemmoma', 'neurilemmoma of twelfth cranial nerve', 'schwannoma of the hypoglossal nerve', 'schwannoma of the twelfth cranial nerve', 'hypoglossal nerve neurilemmoma', 'neurilemmoma of the twelfth cranial nerve', 'twelfth cranial nerve schwannoma', 'hypoglossal neurilemmoma', 'schwannoma of hypoglossal nerve', 'neurilemmoma of hypoglossal nerve', 'hypoglossal schwannoma']",3197,,,C1335928,,C5434,,,,,,
mondo:0002550,hypoglossal nerve neoplasm,"['hypoglossal nerve tumors', 'tumor of hypoglossal nerve', 'tumour of the hypoglossal nerve', 'hypoglossal nerve tumours', 'tumour of hypoglossal nerve', 'tumor of twelfth cranial nerve', 'twelfth cranial nerve tumors', 'hypoglossal nerve tumor', 'twelfth cranial nerve tumour', 'tumor of the hypoglossal nerve', 'hypoglossal nerve neoplasm', 'neoplasm of the hypoglossal nerve', 'XIIth cranial nerve tumours', 'twelfth cranial nerve tumours', 'twelfth cranial nerve neoplasms', 'tumour of the twelfth cranial nerve', 'hypoglossal nerve tumour', 'tumour of twelfth cranial nerve', 'neoplasm of twelfth cranial nerve', 'twelfth cranial nerve neoplasm', 'tumor of the twelfth cranial nerve', 'hypoglossal nerve neoplasms', 'hypoglossal nerve neoplasm (disease)', 'neoplasm of the twelfth cranial nerve', 'XIIth cranial nerve neoplasms', 'XIIth cranial nerve tumors', 'twelfth cranial nerve tumor', 'neoplasm of hypoglossal nerve']",3198,,,C1263903,,C5830,,,239.7,,,
mondo:0002551,c-P angle neurinoma,"['cerebellopontine angle schwannoma', 'cerebellopontine angle neurinoma', 'cerebellar Pontine angle neurinoma']",3199,,,C1332905,,C5413,,,,,,
mondo:0002552,vascular myelopathy,['vascular myelopathies'],320,,,C0154685,,,,,336.1,G95.1,,
mondo:0002553,cerebellopontine angle tumor,"['tumor of C-P angle', 'C-P angle neoplasm', 'tumor of cerebellar Pontine angle', 'tumour of the cerebellar Pontine angle', 'neoplasm of C-P angle', 'C-P angle tumour', 'cerebellar Pontine angle tumor', 'tumour of the C-P angle', 'cerebellopontine angle neoplasm (disease)', 'tumour of C-P angle', 'neoplasm of cerebellar Pontine angle', 'neoplasm of the cerebellopontine angle', 'tumor of cerebellopontine angle', 'cerebellar Pontine angle tumour', 'tumour of the cerebellopontine angle', 'tumour of cerebellopontine angle', 'tumour of cerebellar Pontine angle', 'cerebellar Pontine angle neoplasm', 'neoplasm of the C-P angle', 'tumor of the cerebellar Pontine angle', 'cerebellopontine angle neoplasm', 'neoplasm of the cerebellar Pontine angle', 'tumor of the C-P angle', 'tumor of the cerebellopontine angle', 'neoplasm of cerebellopontine angle', 'C-P angle tumor', 'cerebellopontine angle tumor']",3200,,,,,C5414,,,,,,
mondo:0002554,sympathetic neurilemmoma,['sympathetic schwannoma'],3201,,,C1336543,,C5421,,,,,,
mondo:0002555,trigeminal schwannoma,"['trigeminal nerve schwannoma', 'schwannoma of trigeminal nerve', 'neurilemmoma of fifth cranial nerve', 'fifth cranial nerve schwannoma', 'fifth cranial nerve neurilemmoma', 'neurilemmoma of the trigeminal nerve', 'schwannoma of the trigeminal nerve', 'neurilemmoma of trigeminal nerve', 'trigeminal neurilemmoma', 'trigeminal schwannoma', 'neurilemmoma of the fifth cranial nerve', 'schwannoma of fifth cranial nerve', 'schwannoma of the fifth cranial nerve']",3202,,,C0349582,,C4655,,,215.9,,,
mondo:0002556,microcystic/reticular schwannoma,['microcystic/reticular schwannoma'],,,,C4054526,,C5321,,,,,,
mondo:0002558,melanotic neurilemmoma,"['melanocytic neurilemmoma', 'melanotic neurinoma', 'melanocytic schwannoma', 'pigmented neurilemmoma', 'melanotic schwannoma (morphologic abnormality)', 'MSCHW', 'pigmented schwannoma', 'melanotic schwannoma']",3205,,,C1306247,,C6970,,,215.8,,,
mondo:0002559,plexiform schwannoma,"['plexiform schwannoma (morphologic abnormality)', 'plexiform schwannoma', 'plexiform neurilemmoma', 'plexiform neurinoma']",3206,,,C1370659,,C6969,,,215.9,,,
mondo:0002561,lysosomal storage disease,"['disorder of lysosomal enzymes', 'inborn lysosomal enzyme disorder', 'lysosomal storage disorder', 'lysosomal storage metabolism disorder', 'disorder of lysosomal enzyme', 'lysosomal disease', 'phospholipidosis']",3211,,68366,CN205533,,C61250,,D016464,,,,
mondo:0002562,demyelinating disease,['demyelinating disorder'],3213,,,C0011303,,C34527,,D003711,,,,
mondo:0002563,jejunal somatostatinoma,"['jejunal somatostatin producing tumor', 'jejunal somatostatin-producing NET', 'Delta cell tumour of jejunum', 'Delta cell tumor of the jejunum', 'jejunal somatostatin-producing neuroendocrine tumor', 'jejunal somatostatin producing tumour', 'Somatosatinoma of jejunum', 'jejunal delta cell somatostatin producing tumour', 'Delta cell tumor of jejunum', 'jejunal delta cell somatostatin producing tumor', 'Somatosatinoma of the jejunum', 'jejunal somatostatin-producing neuroendocrine tumour', 'Delta cell tumour of the jejunum']",3216,,,C1334297,,C5787,,,,,,
mondo:0002564,jejunal neoplasm,"['jejunal tumor', 'tumour of the jejunum', 'jejunum neoplasm (disease)', 'tumour of jejunum', 'tumor of jejunum', 'jejunum tumour', 'jejunal tumour', 'neoplasm of jejunum', 'tumor of the jejunum', 'neoplasm of the jejunum', 'jejunum tumor']",3218,,,C0022374,,C8401,,D007580,,,,
mondo:0002565,myelitis,['spinal cord inflammation'],322,,,C0026975,,C26832,1001472,D009187,323.9,,,
mondo:0002567,tracheal disorder,"['trachea disease or disorder', 'disease of trachea', 'disorder of trachea', 'trachea disease', 'tracheal disorder']",3225,,,C0040580,,C35079,,D014133,,,,
mondo:0002568,tracheal stenosis,['stenosis of trachea'],3227,,,C0040583,,C78646,,D014135,519.19,,,
mondo:0002569,gastric dilatation,['stomach dilatation'],3229,,,C0038353,,,,D013271,,,,
mondo:0002570,high pressure neurological syndrome,,3230,,,C0019537,,,,D006610,,,,
mondo:0002571,primary central nervous system lymphoma,"['malignant lymphomas of the CNS', 'CNS lymphoma', 'lymphoma of central nervous system', 'primary central nervous system lymphoma', 'primary lymphoma, CNS', 'central nervous system lymphoma', 'PCNSL', 'malignant lymphomas of CNS', 'primary brain lymphoma', 'microglioma', 'primary CNS lymphoma']",3234,,46135,C0742472,,C9301,1000157,,200.5,,10036685,
mondo:0002572,aspiration pneumonitis,"['aspiration pneumonia', 'chemical pneumonitis']",3240,,,C1761609,,C34932,,D011015,,,,
mondo:0002574,prostate embryonal rhabdomyosarcoma,"['embryonal rhabdomyosarcoma of the prostate', 'embryonal rhabdomyosarcoma of prostate', 'prostate gland embryonal rhabdomyosarcoma (disease)', 'prostate embryonal rhabdomyosarcoma']",3251,,,C1335508,,C5525,,,,,,
mondo:0002576,embryonal extrahepatic bile duct rhabdomyosarcoma,"['extrahepatic bile duct embryonal rhabdomyosarcoma', 'extrahepatic bile duct embryonal rhabdomyosarcoma (disease)', 'embryonal rhabdomyosarcoma of extrahepatic bile duct', 'embryonal extrahepatic bile duct rhabdomyosarcoma', 'embryonal rhabdomyosarcoma of the extrahepatic bile duct']",3253,,,C1333505,,C5847,,,,,,
mondo:0002577,extrahepatic bile duct rhabdomyosarcoma,"['extrahepatic bile duct rhabdomyosarcoma', 'rhabdomyosarcoma of extrahepatic bile duct', 'rhabdomyosarcoma of the extrahepatic bile duct', 'bile duct rhabdomyosarcoma', 'bile duct rhabdomyosarcoma (disease)', 'extrahepatic bile duct rhabdomyosarcoma (disease)', 'rhabdomyosarcoma of the bile duct']",3254,,,C2064434,,C5860,,,,,,
mondo:0002578,botryoid rhabdomyosarcoma,"['botryoid sarcoma (morphologic abnormality)', 'botryoid sarcoma', 'botryoid-type embryonal rhabdomyosarcoma', 'sarcoma botryoides']",3255,,,C1306574,,C9150,,,171.9,,,
mondo:0002579,orbit embryonal rhabdomyosarcoma,"['embryonal rhabdomyosarcoma of orbit', 'embryonal rhabdomyosarcoma of the orbit']",3258,,,C1335127,,C6246,,,,,,
mondo:0002580,orbit rhabdomyosarcoma,"['orbital region rhabdomyosarcoma (disease)', 'rhabdomyosarcoma of orbit', 'rhabdomyosarcoma of the orbit']",3259,,,C0346347,,C4543,,C537605,,,,
mondo:0002581,spindle cell rhabdomyosarcoma,"['spindle cell rhabdomyosarcoma (morphologic abnormality)', 'SCRMS']",3260,,,C1266134,,C6519,,,171.9,,,
mondo:0002582,subacute leukemia,,3264,,,C0153924,,,,,208.20,,,
mondo:0002583,mucinous ovarian cystadenoma,"['benign ovarian mucinous cystadenoma', 'ovarian mucinous cystadenoma', 'benign mucinous cystadenoma of ovary', 'mucinous cystadenoma of ovary', 'ovary mucinous cystadenoma', 'mucinous cystadenoma of the ovary', 'benign mucinous cystadenoma of the ovary']",3267,,,C0346172,,C4512,,,,,,
mondo:0002585,"breast fibrocystic change, proliferative type","['fibrocystic disease, proliferative type with atypia', 'proliferating lesion of breast without atypia', 'fibrocystic change, proliferative type with atypia', 'proliferative type fibrocystic change of the breast', 'benign proliferative breast disease', 'breast fibrocystic change, proliferative type', 'proliferative breast lesion', 'proliferative type fibrocystic change of breast', 'proliferative fibrocystic change', 'proliferative breast disease', 'proliferating lesion of the breast without atypia']",3274,,,C0334056,,C6940,,,,,,
mondo:0002586,thymus cancer,"['cancer of thymus', 'cancer of the Thymus', 'thymus cancer', 'malignant tumor of Thymus', 'malignant tumor of the Thymus', 'thymic tumor', 'thymic neoplasm', 'malignant thymus neoplasm', 'malignant tumour of Thymus', 'malignant Thymus tumour', 'malignant Thymus neoplasm', 'cancer of Thymus', 'malignant neoplasm of thymus', 'thymic tumour', 'malignant neoplasm of the Thymus', 'Thymus cancer', 'malignant neoplasm of Thymus', 'malignant Thymus tumor', 'malignant tumour of the Thymus']",3277,,,C0751552,,C4962,,,164.0,,,
mondo:0002587,encapsulated thymoma,['encapsulated thymoma'],3278,,,C1333383,,C7386,,,,,,
mondo:0002588,thymoma type A,"['primary thymic epithelial neoplasm type A', 'primary thymic epithelial tumor type A', 'thymoma, medullary', 'primary thymic epithelial tumour type A', 'thymoma type A', 'medullary thymoma', 'spindle cell thymoma']",3279,,263310,C1266091,,C6454,,,,D15.0,,
mondo:0002590,combined thymoma,,3281,,,,,,,,,,,
mondo:0002592,invasive malignant thymoma,"['invasive malignant thymoma', 'thymoma malignant invasive', 'infiltrating thymoma', 'malignant thymoma, invasive']",3283,,,C0278846,,C7904,,,,,,
mondo:0002594,monkeypox,"['infections, Monkeypox virus', 'Monkeypox virus infection']",3292,,,C0276180,,C128421,,D045908,136.8,B04,,
mondo:0002595,vaccinia,,3298,,,C0042214,,,,D014615,999.0,,,
mondo:0002597,notochordal tumor,"['malignant neoplasm of notochord', 'notochordal tumor', 'tumour of notochord', 'notochordal neoplasm', 'cancer of notochord', 'neoplasm of notochord', 'malignant notochord neoplasm', 'notochordal cancer', 'notochord tumour', 'tumor of notochord', 'notochord cancer', 'notochord tumor']",3303,,,C1335069,,C7063,,,,,,
mondo:0002598,germinoma,"['germinoma (disease)', 'germinoma']",3304,,,C0206660,,C3753,,D018237,,,,0100620
mondo:0002599,teratocarcinoma,"['mixed embryonal carcinoma and teratoma', 'teratocarcinoma (morphologic abnormality)', 'teratocarcinoma']",3305,,,C0206664,,C3756,,D018243,,,,
mondo:0002601,teratoma,['teratoma'],3307,,,,,C3403,,D013724,,,,
mondo:0002602,central nervous system disorder,"['disease of the central nervous system', 'central nervous system disorder', 'disease of central nervous system', 'CNS disorder', 'central nervous system disease', 'central nervous system disease or disorder', 'disorder of central nervous system', 'central nervous disease']",331,,,C0007682,,C2934,,D002493,,,,
mondo:0002603,angiomyolipoma,['angiomyolipoma (morphologic abnormality)'],3314,,,C0206633,,C3734,,D018207,,,,
mondo:0002604,pericytic neoplasm,"['Pericytic tumour', 'perivascular tumor', 'Pericytic tumor', 'malignant perivascular cancer', 'Pericytic neoplasm', 'perivascular tumour', 'perivascular neoplasm']",3316,,,C1335392,,C6528,,,,,,
mondo:0002605,hepatic angiomyolipoma,"['liver angiomyolipoma', 'liver PEComa']",3317,,,C1333962,,C27485,,,,,,
mondo:0002606,epithelioid type angiomyolipoma,,3318,,,C1333426,,C38151,,,,,,
mondo:0002610,purpura,"['purpura', 'purpuric disorder', 'purpura (disease)']",3326,,,C0034150,,,,D011693,,,,0000979
mondo:0002612,frontal lobe epilepsy,"['epilepsy of frontal lobe', 'frontal lobe epilepsy']",3331,,,C0085541,,,,D017034,,,,
mondo:0002613,histrionic personality disorder,"['histrionic personality disorder', 'histrionic personality disorder (disease)']",334,,,,,C92634,,D006677,301.59,F60.4,,0012077
mondo:0002614,bone inflammation disease,"['osteitis', 'inflammatory disorder of bone', 'bone inflammatory disease']",3342,,,C0029400,,,,D010000,,,,
mondo:0002615,xanthomatosis,"['xanthomatosis (disease)', 'xanthomatosis', 'xanthelasmatosis']",3345,,,C0043325,,,,D014973,,,,0000991
mondo:0002616,mesenchymal cell neoplasm,"['mesenchymal cell tumor', 'benign miscellaneous mesenchymal tumor', 'mesenchymal cell tumour', 'mesenchymal tumour', 'benign miscellaneous mesenchymal tumour', 'mesenchymal cell neoplasm', 'mesenchymal neoplasm', 'mesenchymal tumor']",3350,,,C1334699,,C7059,,,,,,
mondo:0002617,bone angiosarcoma,"['osseous angioendothelial sarcoma', 'bone tissue angiosarcoma (disease)', 'bone angioendothelial sarcoma', 'bone hemangiosarcoma', 'osseous hemangiosarcoma', 'bone angiosarcoma', 'bone Hemangioendothelial sarcoma', 'osseous angiosarcoma']",3351,,,C1332574,,C6479,,,,,,
mondo:0002618,undifferentiated high grade pleomorphic sarcoma of bone,"['malignant bone fibrous histiocytoma', 'undifferentiated high grade pleomorphic sarcoma of bone', 'undifferentiated high grade pleomorphic sarcoma', 'undifferentiated high-grade pleomorphic sarcoma', 'malignant fibrous histiocytoma of the bone', 'malignant fibrous histiocytoma of bone']",3352,,,C0740479,,C8563,,,,,,
mondo:0002619,bone fibrosarcoma,"['bone tissue fibrosarcoma (disease)', 'fibrosarcoma of bone', 'fibrosarcoma of the bone', 'bone fibrosarcoma']",3354,,,C2733623,,C6604,,,,,,
mondo:0002620,localized osteosarcoma,"['osteosarcoma, localized', 'localized osteogenic sarcoma', 'localised osteogenic sarcoma', 'localized osteosarcoma', 'osteosarcoma, localised']",3356,,,C0278511,,C7780,,,,,,
mondo:0002621,extraosseous osteosarcoma,"['extraskeletal osteogenic sarcoma', 'osteosarcoma, extraskeletal, malignant', 'extraskeletal osteosarcoma', 'soft tissue osteosarcoma', 'extraosseous osteosarcoma']",3357,,,C0855052,,C8810,,,170.9,,,
mondo:0002622,multifocal osteogenic sarcoma,"['multifocal osteosarcoma', 'multicentric osteosarcoma']",3360,,,C1334820,,C6470,,,,,,
mondo:0002623,pediatric osteosarcoma,"['childhood osteogenic sarcoma', 'childhood osteosarcoma', 'osteosarcoma', 'pediatric osteosarcoma', 'pediatric osteosarcoma (disease)', 'osteosarcoma (disease) of childhood', 'paediatric osteosarcoma (disease)']",3361,,,C1332986,,C6585,,,,,,
mondo:0002624,bone leiomyosarcoma,"['leiomyosarcoma of bone tissue', 'bone leiomyosarcoma', 'bone tissue leiomyosarcoma', 'leiomyosarcoma of bone']",3367,,,C1332579,,C7154,,,,,,
mondo:0002625,Ewing sarcoma of bone,"['bone Ewing^s sarcoma', 'localised skeletal Ewing^s sarcoma', 'Ewing^s sarcoma of bone', 'osseous Ewing^s tumour', 'bone Ewing sarcoma', 'osseous Ewing^s tumor', 'localized skeletal Ewing^s sarcoma', 'osseous Ewing^s sarcoma', 'bone localized Ewing^s sarcoma', 'Ewing^s sarcoma/bone peripheral primitive neuroectodermal tumour', 'skeletal Ewing^s tumor', 'Ewing^s sarcoma/bone peripheral primitive neuroectodermal tumor', 'bone localised Ewing^s sarcoma', 'Ewing^s sarcoma, osseous', 'bone localized Ewing sarcoma', 'skeletal Ewing^s tumour', 'skeletal Ewing^s sarcoma', 'bone tissue Ewing sarcoma', 'bone localised Ewing sarcoma', 'Ewing sarcoma of bone']",3368,,,C0585474,,C4835,,,170.9,,,
mondo:0002626,spinal accessory nerve neoplasm,"['tumor of accessory XI nerve spinal component', 'spinal accessory nerve neoplasms', 'tumour of the eleventh cranial nerve', 'tumor of the eleventh cranial nerve', 'neoplasm of the eleventh cranial nerve', 'tumor of the spinal accessory nerve', 'neoplasm of accessory nerve', 'eleventh cranial nerve tumours', 'neoplasm of the spinal accessory nerve', 'tumor of eleventh cranial nerve', 'spinal accessory nerve tumours', 'eleventh cranial nerve neoplasms', 'XIth cranial nerve neoplasms', 'spinal accessory nerve tumour', 'spinal accessory nerve neoplasm', 'tumour of accessory XI nerve spinal component', 'eleventh cranial nerve tumors', 'tumor of spinal accessory nerve', 'neoplasm of spinal accessory nerve', 'accessory nerve neoplasm', 'eleventh cranial nerve tumour', 'accessory XI nerve spinal component tumour', 'accessory XI nerve spinal component tumor', 'XIth cranial nerve tumours', 'tumour of the spinal accessory nerve', 'eleventh cranial nerve neoplasm', 'neoplasm of eleventh cranial nerve', 'eleventh cranial nerve tumor', 'spinal accessory nerve tumors', 'accessory XI nerve spinal component neoplasm (disease)', 'XIth cranial nerve tumors', 'tumour of spinal accessory nerve', 'neoplasm of accessory XI nerve spinal component', 'spinal accessory nerve tumor', 'tumour of eleventh cranial nerve']",337,,,C1263902,,C5829,,,239.7,,,
mondo:0002627,chondroblastic osteosarcoma,"['chondroblastic osteosarcoma (morphologic abnormality)', 'chondrosarcomatous osteogenic sarcoma', 'chondroblastic osteogenic sarcoma', 'CHOS', 'chondroblastic osteosarcoma']",3372,,,C0279603,,C4021,,,,,,
mondo:0002628,peripheral osteosarcoma,"['surface osteosarcoma', 'bone surface (peripheral) osteosarcoma', 'peripheral osteosarcoma']",3374,,,C1332591,,C7134,,,,,,
mondo:0002629,bone osteosarcoma,"['osteosarcoma, somatic', 'bone osteosarcoma', 'osteosarcoma of bone', 'primary osteosarcoma of bone', 'osteosarcoma, somatic mutation']",3376,259500,668,,"['-0.012886', '0.02809', '0.04074', '-0.02545', '0.02553', '-0.04175', '0.00873', '0.0828', '-0.0349', '-0.02701', '-0.006737', '0.01315', '-0.002972', '0.03647', '-0.02162', '-0.02989', '-0.01072', '-0.029', '-0.02425', '-0.091', '-0.0009575', '-0.02058', '0.03384', '-0.0321', '0.02808', '-0.00931', '0.004604', '-0.006893', '-0.0162', '-0.0173', '0.03784', '-0.0292', '0.06198', '0.00972', '0.00694', '-0.01245', '-0.01288', '-0.04276', '-0.014694', '-0.05618', '0.007366', '-0.03635', '0.03696', '-0.04758', '-0.0001035', '-0.03275', '-0.01001', '0.03568', '0.0302', '0.00749', '0.00418', '-0.003483', '0.02458', '0.02475', '-0.0398', '-0.0261', '0.03583', '-0.03091', '-0.0699', '-0.01863', '0.071', '0.02559', '-0.03262', '-0.0207', '-0.002691', '0.02528', '0.0562', '0.059', '-0.01659', '0.0727', '-0.03375', '0.001188', '-0.00859', '-0.04703', '0.03726', '0.02109', '-0.007755', '-0.011345', '-0.01063', '-0.06274', '-0.02853', '0.01881', '-0.02234', '0.0524', '-0.06055', '-0.003345', '0.01949', '0.03555', '0.06256', '0.01273', '0.01079', '0.02861', '-0.0148', '0.0113', '0.08636', '0.03096', '0.04892', '-0.08167', '0.01347', '0.01395']",C53707,,,170.9,,10031291,
mondo:0002630,small cell osteogenic sarcoma,"['SCOS', 'small cell osteosarcoma', 'round cell osteosarcoma']",3377,,,C0279622,,C4023,,,,,,
mondo:0002631,conventional osteosarcoma,"['central osteosarcoma', 'intracortical osteosarcoma (morphologic abnormality)', 'conventional central osteosarcoma', 'intracortical osteosarcoma', 'intracortical osteogenic sarcoma', 'conventional osteosarcoma', 'medullary osteosarcoma']",7602,,,C1266166,,C35870,,,,,,
mondo:0002632,metachronous osteosarcoma of the bone,"['metachronous osteosarcoma', 'metachronous osteosarcoma of the bone']",3379,,,C1334704,,C38157,,,,,,
mondo:0002633,cranial nerve neoplasm,"['tumor of the cranial nerve', 'tumour of cranial nerve', 'neoplasm of the cranial nerve', 'cranial nerve neoplasms', 'cranial nerve tumor', 'tumor of cranial nerve', 'neoplasm of cranial nerve', 'cranial nerve tumour', 'cranial nerve neoplasm (disease)', 'tumour of the cranial nerve', 'cranial nerve neoplasm']",338,,,C0010267,,C2963,,D003390,239.7,,,
mondo:0002634,liposarcoma of bone,"['bone liposarcoma', 'liposarcoma of bone tissue', 'bone tissue liposarcoma', 'liposarcoma of the bone', 'liposarcoma of bone']",3381,,,C1332581,,C7598,,,,,,
mondo:0002635,periodontal disorder,"['disease of supporting structures of teeth', 'disease of periodontium', 'periodontium disease', 'periodontal disease', 'disorder of periodontium', 'periodontal disorder', 'periodontium disorder', 'periodontium disease or disorder']",3388,,,C0031090,,C63743,,D010510,523.8,,,
mondo:0002636,accessory nerve disorder,"['accessory XI nerve disease or disorder', 'disorder of accessory [11th] nerve', 'disorder of accessory XI nerve', 'eleventh nerve disorder', 'disorder of 11th nerve', 'disorder of accessory nerve', 'disorder of the 11th nerve', 'disease of accessory XI nerve', 'accessory nerve disorder', 'accessory XI nerve disease']",339,,,C0152180,,C26953,,D020436,352.4,,,
mondo:0002637,histiocytosis,"['histiocytic and dendritic cell neoplasms', 'hand Schuller Christian disease', 'chronic histiocytosis X', 'histiocytic infiltrate', 'histiocytic syndrome']",3405,,,C0019618,,C3106,,D015614,,,,
mondo:0002638,glossopharyngeal nerve neoplasm,"['tumour of the Ninth cranial nerve', 'tumour of glossopharyngeal nerve', 'glossopharyngeal nerve tumour', 'glossopharyngeal nerve tumors', 'IXth cranial nerve neoplasms', 'Ninth cranial nerve tumor', 'tumour of the glossopharyngeal nerve', 'tumor of Ninth cranial nerve', 'Ninth cranial nerve tumour', 'tumour of Ninth cranial nerve', 'glossopharyngeal nerve neoplasms', 'glossopharyngeal nerve neoplasm (disease)', 'Ninth cranial nerve neoplasm', 'glossopharyngeal nerve tumours', 'IXth cranial nerve tumours', 'tumor of glossopharyngeal nerve', 'Ninth cranial nerve neoplasms', 'neoplasm of Ninth cranial nerve', 'glossopharyngeal nerve neoplasm', 'tumor of the glossopharyngeal nerve', 'glossopharyngeal nerve tumor', 'tumor of the Ninth cranial nerve', 'IXth cranial nerve tumors', 'neoplasm of the Ninth cranial nerve', 'Ninth cranial nerve tumours', 'neoplasm of glossopharyngeal nerve', 'neoplasm of the glossopharyngeal nerve', 'Ninth cranial nerve tumors']",3417,,,C1263900,,C5828,,,239.7,,,
mondo:0002639,glossopharyngeal nerve disorder,"['disorder of glossopharyngeal nerve', 'glossopharyngeal nerve disease', 'glossopharyngeal nerve disease or disorder', 'disease of glossopharyngeal nerve', 'ninth nerve disorder', 'glossopharyngeal nerve disorder', 'IX nerve disorder']",3418,,,C0751941,,C27211,,,352.2,,,
mondo:0002640,optic nerve neoplasm,"['optic nerve neoplasm', 'tumour of the optic nerve', 'tumor of the second cranial nerve', 'second cranial nerve neoplasms', 'cranial nerve II neoplasm (disease)', 'second cranial nerve tumor', 'neoplasm of the optic nerve', 'cranial nerve II neoplasms', 'cranial nerve II tumour', 'tumor of the optic nerve', 'neoplasm of cranial nerve II', 'neoplasm of optic nerve', 'neoplasms, second cranial nerve', 'tumour of second cranial nerve', 'second cranial nerve tumour', 'tumour of optic nerve', 'tumour of cranial nerve II', 'neoplasm of the second cranial nerve', 'tumor of cranial nerve II', 'optic nerve tumor', 'optic nerve neoplasms', 'second cranial nerve neoplasm', 'tumor of optic nerve', 'neoplasm of second cranial nerve', 'tumour of the second cranial nerve', 'neoplasms, optic nerve', 'optic nerve tumour', 'cranial nerve II tumor', 'tumor of second cranial nerve']",3419,,,C0524802,,C4801,1001073,D019574,239.7,,,
mondo:0002641,subclavian artery aneurysm,,342,,,C0155746,,,,,442.82,,,
mondo:0002642,trochlear nerve neoplasm,"['IVth cranial nerve neoplasms', 'fourth cranial nerve tumours', 'IVth cranial nerve tumours', 'neoplasm of trochlear nerve', 'tumor of fourth cranial nerve', 'fourth cranial nerve tumor', 'trochlear nerve tumors', 'trochlear nerve neoplasm (disease)', 'trochlear nerve tumor', 'tumour of the trochlear nerve', 'neoplasm of the fourth cranial nerve', 'fourth cranial nerve tumors', 'trochlear nerve tumours', 'IVth cranial nerve tumors', 'trochlear nerve neoplasms', 'fourth cranial nerve neoplasms', 'tumour of the fourth cranial nerve', 'fourth cranial nerve neoplasm', 'tumor of the fourth cranial nerve', 'fourth cranial nerve tumour', 'tumour of fourth cranial nerve', 'neoplasm of the trochlear nerve', 'neoplasm of fourth cranial nerve', 'trochlear nerve tumour', 'tumour of trochlear nerve', 'tumor of trochlear nerve', 'tumor of the trochlear nerve']",3421,,,C1263896,,C5825,,,239.7,,,
mondo:0002643,vestibular disorder,"['disease of vestibular labyrinth', 'disorder of vestibular labyrinth', 'vertigo, vestibular disorder', 'vestibular labyrinth disease', 'disorder of vestibular system', 'vestibular labyrinth disease or disorder', 'disease of vestibular system', 'vestibular system disease']",3426,,,C0042594,,,,D015837,,,,
mondo:0002644,idiopathic granulomatous myositis,"['granulomatous myositis', 'idiopathic granulomatous myositis']",3428,,206979,C1334150,,C27575,,,,,,
mondo:0002645,cerebritis,['cerebral hemisphere inflammation'],3431,,,C0742115,,C27199,,,,,,
mondo:0002646,viral laryngitis,['Viruses caused laryngitis'],3436,,,C0853195,,C27305,,,464.00,,,
mondo:0002647,laryngitis,"['laryngeal inflammation', 'laryngeal Inflammation', 'larynx inflammation']",3437,,,C0023067,,C26811,,D007827,464.00,,,
mondo:0002648,mammary Paget disease,"['Paget cell neoplasm', 'mammary Paget^s disease', 'mammary Paget disease', 'Paget^s disease of the breast', 'breast Paget disease', 'Paget disease of the breast', 'Paget^s disease of breast']",3443,,,CN200478,,C47857,,D010144,,,,
mondo:0002649,scrotum Paget disease,"['scrotum Paget^s disease', 'Paget disease of the scrotum', 'Paget^s disease of scrotum', 'scrotal Paget^s disease', 'scrotum mammary Paget^s disease', 'scrotum Paget disease', 'Paget^s disease of the scrotum']",3444,,,C0238330,,C7728,,,,,,
mondo:0002650,scrotal carcinoma,"['carcinoma of the scrotum', 'scrotal cancer', 'cancer of scrotum', 'cancer of the scrotum', 'carcinoma of scrotum', 'scrotum carcinoma']",3445,,,C1370468,,C6389,,,,,,
mondo:0002651,anal Paget disease,"['anus Paget disease', 'Paget^s disease of anus', 'anus mammary Paget^s disease', 'Paget^s disease of the anus', 'anal Paget^s disease', 'Paget disease of the anus', 'anal Paget disease']",3446,,,C1332274,,C5598,,,,,,
mondo:0002652,anus adenocarcinoma,"['adenocarcinoma of anus', 'anal adenocarcinoma', 'anus adenocarcinoma', 'adenocarcinoma of the anus']",3447,,,C1332257,,C5600,,,,,,
mondo:0002653,Paget disease of the penis,"['Paget disease of the penis', 'Paget^s disease of penis', 'penis adenocarcinoma', 'penile adenocarcinoma', 'adenocarcinoma of penis', 'penis Paget disease', 'penis mammary Paget^s disease', 'Paget^s disease of the penis', 'adenocarcinoma of the penis', 'penis Paget^s disease']",3448,,398053,C0221286,,C27817,,,,,,
mondo:0002654,uterine disorder,"['disease of uterus', 'disorder of uterus', 'uterus disease', 'uterine disease', 'uterine disorder', 'uterus disease or disorder']",345,,,C0042131,,C26907,,D014591,621.9,,,
mondo:0002655,cutaneous Paget disease,"['extramammary Paget^s disease', 'cutaneous Paget^s disease', 'cutaneous Paget disease', 'zone of skin Paget disease']",3450,,,,,C3302,,D010145,,,,
mondo:0002656,skin carcinoma,"['carcinoma of zone of skin', 'non-melanoma cancer of the skin', 'carcinoma of the skin', 'skin carcinoma', 'carcinoma of skin', 'zone of skin carcinoma', 'non-melanoma cancer of skin', 'non-melanoma skin cancer', 'skin cancer, non-melanoma', 'nonmelanoma skin cancer']",3451,,,C0699893,,C4914,,,,,,
mondo:0002657,breast disorder,"['breast disease or disorder', 'breast disease', 'breast disorder', 'breast diseases', 'disorder of breast', 'disease of breast']",3463,,,C0006145,,C26709,,D001941,611.9,N60-N65,,
mondo:0002658,iris cancer,"['malignant tumour of iris', 'malignant iris tumour', 'malignant neoplasm of the iris', 'malignant tumor of the iris', 'malignant iris tumor', 'iris cancer', 'malignant tumor of iris', 'malignant iris neoplasm', 'cancer of iris', 'tumor of the iris', 'malignant tumour of the iris', 'malignant neoplasm of iris', 'tumour of the iris']",3478,,,C0346372,,C4554,1000996,,,,,
mondo:0002659,uveal cancer,"['malignant uvea tumor', 'malignant tumour of uvea', 'malignant tumour of the uvea', 'cancer of uvea', 'malignant uveal tumor', 'malignant tumor of the uvea', 'malignant uvea neoplasm', 'malignant uveal tumour', 'malignant neoplasm of the uvea', 'uveal tumor', 'malignant uvea tumour', 'uvea cancer', 'malignant tumor of uvea', 'uveal tumour', 'malignant uveal neoplasm', 'malignant neoplasm of uvea']",3479,,,C1334629,,C6105,1001230,,,,,
mondo:0002660,blepharochalasis,"['blepharochalasis (disease)', 'blepharochalasis']",348,,,C0005742,,,,,374.34,H02.3,,0010749
mondo:0002661,uveal disorder,"['uveal diseases', 'disorder of uveal tract', 'disorder of uvea', 'disease of uvea', 'uveal disorder', 'uvea disease', 'uveal tract disease', 'uvea disease or disorder', 'uveal disease']",3480,,,C0042161,,C26908,,D014603,,,,
mondo:0002664,extrahepatic bile duct signet ring cell carcinoma,"['signet Ring cell bile duct carcinoma', 'signet Ring cell carcinoma of bile duct', 'signet Ring cell carcinoma of the bile duct', 'extrahepatic bile duct signet Ring cell carcinoma', 'bile duct signet Ring cell carcinoma', 'bile duct signet ring cell carcinoma']",3494,,,C0861859,,C5776,,,,,,
mondo:0002665,extrahepatic bile duct adenocarcinoma,"['adenocarcinoma of extrahepatic bile duct', 'adenocarcinoma of the extrahepatic bile duct', 'extrahepatic bile duct adenocarcinoma']",3495,,,C0279659,,C7975,,,,,,
mondo:0002666,pancreatic signet ring cell adenocarcinoma,"['pancreatic signet ring cell carcinoma', 'signet Ring cell carcinoma of pancreas', 'pancreas signet ring cell carcinoma', 'signet Ring cell carcinoma of the pancreas', 'pancreatic signet Ring cell carcinoma']",3497,,,C1335317,,C5720,,,,,,
mondo:0002667,gallbladder signet ring cell adenocarcinoma,"['signet Ring cell carcinoma of the gallbladder', 'signet Ring cell carcinoma of gallbladder', 'gall bladder signet ring cell carcinoma', 'gallbladder signet Ring cell carcinoma']",3499,,,C1333758,,C5745,,,,,,
mondo:0002669,ampullary signet ring cell adenocarcinoma,"['ampulla of Vater signet Ring cell carcinoma', 'ampullary signet Ring cell carcinoma', 'ampullary signet ring cell carcinoma']",3501,,,C1332249,,C6656,,,,,,
mondo:0002670,ampulla of vater adenocarcinoma,"['ampullary adenocarcinoma', 'adenocarcinoma of ampulla of Vater', 'adenocarcinoma of ampulla of vater', 'ampulla of Vater adenocarcinoma', 'invasive adenocarcinoma of the ampullary region', 'hepatopancreatic ampulla adenocarcinoma']",3502,,,C1332243,,C6650,0008490,,,,,
mondo:0002671,signet ring cell breast carcinoma,"['primary signet Ring cell carcinoma of the breast', 'signet Ring cell breast carcinoma', 'primary signet Ring cell carcinoma of breast', 'breast signet ring cell adenocarcinoma', 'breast carcinoma with signet ring', 'SRC breast carcinoma', 'breast signet ring cell carcinoma', 'primary signet Ring cell breast carcinoma', 'mammary signet Ring cell carcinoma', 'SRC carcinoma of the breast', 'signet ring cell carcinoma of breast', 'primary SRC breast carcinoma', 'primary mammary signet Ring cell carcinoma', 'SRC carcinoma of breast', 'primary SRC carcinoma of breast', 'primary SRC carcinoma of the breast', 'signet Ring cell carcinoma of breast', 'signet Ring cell carcinoma of the breast']",3503,,,C1335964,,C5175,,,,,,
mondo:0002672,"acinar prostate adenocarcinoma, signet ring variant","['prostate signet ring cell carcinoma', 'acinar prostate adenocarcinoma, signet Ring variant', 'signet Ring cell carcinoma of the prostate', 'signet Ring cell carcinoma of prostate', 'prostate signet ring cell adenocarcinoma', 'prostate gland signet ring cell carcinoma', 'prostate signet Ring cell carcinoma']",3504,,,C1335520,,C5535,,,,,,
mondo:0002674,stricture or kinking of ureter,,3508,,,,,,,,593.3,,,
mondo:0002675,neurofibrosarcoma,"['neurosarcoma [obs]', 'neurosarcoma']",3512,,,,,,,D018319,,,,
mondo:0002676,adult fibrosarcoma,"['fibrosarcoma (disease) of adults', 'fibrosarcoma', 'adult fibrosarcoma']",3516,,,C0278595,,C7809,,,,,,
mondo:0002677,conventional fibrosarcoma,"['classical fibrosarcoma', 'conventional fibrosarcoma', 'classic fibrosarcoma']",3517,,,C1333156,,C9429,,,,,,
mondo:0002678,pediatric fibrosarcoma,"['pediatric fibrosarcoma', 'childhood fibrosarcoma', 'fibrosarcoma']",3520,,,C0279981,,C8088,,,,,,
mondo:0002679,cerebral infarction,"['infarction, cerebral', 'telencephalon brain infarction', 'brain infarction of telencephalon', 'CVA - cerebral infarction', 'cerebral infarct', 'cerebral, infarction', 'cerebral ischemia', 'cerebral infarction']",3526,,,C0007785,,C50486,,D002544,434.91,,,
mondo:0002680,chronic wasting disease,,3530,,,C1135993,,,,D034081,,,,
mondo:0002681,choroid plexus cancer,"['malignant choroid plexus tumour', 'tumor of choroid plexus', 'malignant choroid plexus tumours', 'choroid plexus neoplasm', 'malignant choroid plexus tumors', 'malignant choroid plexus tumor', 'malignant neoplasm of the choroid plexus', 'malignant tumor of the choroid plexus', 'choroid plexus cancer', 'malignant tumor of choroid plexus', 'cancer of choroid plexus', 'malignant tumour of the choroid plexus', 'malignant choroid plexus neoplasm', 'tumour of choroid plexus', 'malignant tumour of choroid plexus', 'tumour of the choroid plexus', 'malignant neoplasm of choroid plexus', 'malignant choroid plexus neoplasms']",3540,,,,,C4533,,,,,,
mondo:0002682,cerebral ventricle cancer,"['intraventricular neoplasms', 'brain ventricle cancer', 'intraventricular brain neoplasms', 'intraventricular neoplasm of brain', 'intraventricular neoplasm of the brain', 'intraventricular tumour of the brain', 'malignant neoplasm of brain ventricle', 'cancer of brain ventricle', 'intraventricular brain tumour', 'intraventricular tumour of brain', 'intraventricular tumor of brain', 'intraventricular brain neoplasm', 'malignant brain ventricle neoplasm', 'cerebral ventricle neoplasm', 'intraventricular tumor of the brain', 'brain neoplasms, intraventricular', 'intraventricular brain tumor']",3541,,,,,C2937,0007201,D002551,191.5,,,
mondo:0002683,adult choroid plexus neoplasm,"['adult choroid plexus neoplasm', 'choroid plexus neoplasm of adults', 'adult choroid plexus cancer', 'tumour of the adult choroid plexus', 'adult choroid plexus tumour', 'tumor of the adult choroid plexus', 'choroid plexus neoplasm', 'neoplasm of adult choroid plexus', 'tumor of adult choroid plexus', 'tumour of adult choroid plexus', 'adult choroid plexus tumor', 'neoplasm of the adult choroid plexus']",3542,,,C0796430,,C8568,,,,,,
mondo:0002684,atypical choroid plexus papilloma,"['atypical CPP', 'atypical choroid plexus papilloma', 'atypical papilloma of choroid plexus', 'ACPP', 'atypical choroid plexus papilloma (morphologic abnormality)']",3544,,251902,C1266176,,C53686,,,,,,
mondo:0002685,childhood choroid plexus carcinoma,"['childhood choroid plexus cancer', 'paediatric choroid plexus carcinoma', 'choroid plexus carcinoma of childhood', 'childhood choroid plexus neoplasm', 'pediatric choroid plexus carcinoma', 'childhood choroid plexus carcinoma']",3545,,,C0280623,,C124292,,,,,,
mondo:0002687,superior mesenteric artery syndrome,"['Arteriomesenteric duodenal compression syndrome', 'syndromic disease of superior mesenteric artery', 'Cast syndrome', 'superior mesenteric artery syndrome', 'vascular compression of the duodenum', 'Wilkie syndrome', 'superior mesenteric artery syndromic disease']",3557,,622099,C0038828,,C85175,1001201,D013478,,,,
mondo:0002688,duodenal obstruction,,3558,,,C0013292,,,1000908,D004380,,,,
mondo:0002691,liver cancer,"['resectable malignant neoplasm of the liver', 'ca liver - primary', 'hepatic neoplasm', 'malignant neoplasm of liver', 'Resectable malignant neoplasm of liver', 'liver cancer', 'primary tumour of the liver', 'hepatic cancer', 'malignant liver neoplasm', 'Ca liver - primary', 'malignant tumour of liver', 'primary liver cancer', 'primary malignant liver neoplasm', 'malignant neoplasm of liver, primary', 'primary tumor of the liver', 'malignant neoplasm of liver, not specified as primary or secondary', 'cancer of liver', 'primary cancer of liver', 'malignant tumor of liver', 'non-resectable primary hepatic malignant neoplasm', 'primary malignant neoplasm of liver', 'malignant hepato-biliary neoplasm']",3571,,,C0854795,,C34803,,,155.2,,,
mondo:0002692,intracranial sinus thrombosis,,3572,,,C0037198,,,,D012851,,,,
mondo:0002693,lateral sinus thrombosis,"['thrombosis of lateral venous sinus', 'thrombosis transverse sinus']",3574,,,C0270639,,,,D020227,,,,
mondo:0002694,cavernous sinus thrombosis,['thrombosis of cavernous venous sinus'],3575,,,C0238454,,,,D020226,,,,
mondo:0002695,sagittal sinus thrombosis,"['thrombosis of superior longitudinal sinus', 'thrombosis of superior sagittal sinus']",3576,,,C0338575,,,,D020225,,,,
mondo:0002696,Sertoli cell tumor,"['tubular androblastoma', 'Sertoli cell tumor', 'tubular androblastoma NOS (morphologic abnormality)']",3577,,,C0036769,,C39976,,D012707,,,,
mondo:0002697,ovarian gonadoblastoma,"['ovarian gonadoblastoma (disease)', 'ovarian gonadoblastoma', 'gonadoblastoma', 'GBY', 'ovary gonadoblastoma', 'gonadoblastoma of ovary']",3578,424500,206484,C1518716,,C39985,1000420,,,,,0000149
mondo:0002698,testicular gonadoblastoma,"['testis gonadoblastoma', 'testicular gonadoblastoma (disease)', 'testicular gonadoblastoma', 'gonadoblastoma of testis']",3579,,,C1515283,,C39911,,,,,,0000030
mondo:0002701,ovarian mucinous cystadenocarcinoma,"['ovary mucinous cystadenocarcinoma', 'ovarian mucinous cystadenocarcinoma', 'mucinous cystadenocarcinoma of ovary', 'mucinous cystadenocarcinoma of the ovary']",3604,,,C0279665,,C4026,1001963,,,,,
mondo:0002702,ovarian cystadenocarcinoma,"['ovarian cystadenocarcinoma', 'ovary cystadenocarcinoma', 'cystadenocarcinoma of ovary', 'cystadenocarcinoma of the ovary']",3605,,,C1096638,,C5228,1001962,,,,,
mondo:0002703,appendix mucinous cystadenocarcinoma,"['colloidal cystadenocarcinoma of appendix', 'appendiceal colloid cystadenocarcinoma', 'colloidal cystadenocarcinoma of the appendix', 'appendix colloid cystadenocarcinoma', 'appendix colloidal cystadenocarcinoma', 'colloid cystadenocarcinoma of the appendix', 'appendiceal colloidal cystadenocarcinoma', 'mucinous cystadenocarcinoma of appendix', 'appendix mucinous cystadenocarcinoma', 'mucinous cystadenocarcinoma of the appendix', 'vermiform appendix mucinous cystadenocarcinoma', 'colloid cystadenocarcinoma of appendix', 'appendiceal mucinous cystadenocarcinoma']",3607,,,C1096639,,C5511,,,,,,
mondo:0002705,breast mucinous cystadenocarcinoma,['breast mucinous cystadenocarcinoma'],3609,,,C1511318,,C40354,,,,,,
mondo:0002706,cervix endometriosis,"['uterine cervix endometriosis (disease)', 'cervical endometriosis', 'endometriosis of cervix']",361,,,C0269107,,C27623,,,,,,
mondo:0002707,breast mucinous carcinoma,"['breast mucinous carcinoma', 'invasive mucinous breast carcinoma', 'colloid carcinoma of breast', 'colloid breast carcinoma', 'infiltrating colloid breast carcinoma', 'mucinous carcinoma of breast', 'colloid carcinoma of the breast', 'mucinous breast cancer', 'mucinous breast carcinoma', 'infiltrating mucinous breast carcinoma', 'breast invasive mixed mucinous carcinoma', 'invasive colloid breast carcinoma', 'mucinous carcinoma of the breast']",3610,,,C1334807,,C9131,,,,,,
mondo:0002708,retinitis,['retina inflammation'],3612,,,C0035333,,C115993,,D012173,,,,
mondo:0002710,infiltrating angiolipoma,"['angiolipoma, infiltrating', 'infiltrating angiolipoma', 'angiolipoma, infiltrating (morphologic abnormality)']",3615,,,C1305256,,C7449,,,,,,
mondo:0002712,epidural spinal canal angiolipoma,"['angiolipoma of the epidural spinal canal', 'angiolipoma of the extradural spinal canal', 'angiolipoma of extradural spinal canal', 'angiolipoma of epidural spinal canal', 'extradural spinal canal angiolipoma', 'epidural space angiolipoma', 'angiolipoma of epidural space']",3617,,,C1333416,,C5424,,,,,,
mondo:0002713,epidural spinal canal neoplasm,"['neoplasm of epidural space', 'extradural spinal neoplasms', 'epidural tumour', 'extradural spinal tumors', 'epidural spinal tumours', 'neoplasm of the epidural spinal canal', 'tumor of extradural spinal canal', 'epidural spinal canal tumor', 'epidural spinal neoplasms', 'tumour of epidural space', 'tumour of the extradural spinal canal', 'extradural spinal canal tumour', 'epidural tumor', 'neoplasm of the extradural spinal canal', 'tumor of the extradural spinal canal', 'epidural spinal canal tumors', 'epidural spinal canal tumour', 'tumor of epidural space', 'epidural spinal tumors', 'neoplasm of epidural spinal canal', 'extradural spinal canal neoplasm', 'tumour of the epidural spinal canal', 'extradural spinal canal tumor', 'extradural tumour', 'epidural spinal canal neoplasm', 'epidural space tumor', 'tumor of epidural spinal canal', 'tumour of epidural spinal canal', 'extradural spinal tumours', 'epidural space tumour', 'epidural neoplasm', 'epidural spinal canal tumours', 'neoplasm of extradural spinal canal', 'tumor of the epidural spinal canal', 'extradural neoplasm', 'extradural tumor', 'tumour of extradural spinal canal', 'extradural spinal canal neoplasms']",3618,,,C0014536,,C3019,1000923,D015174,,,,
mondo:0002714,central nervous system cancer,"['malignant tumor of the CNS', 'CNS neoplasm', 'malignant tumour of the central nervous system', 'malignant central nervous system tumor', 'CNS malignant neoplasms', 'malignant central nervous system tumour', 'malignant neoplasm of the CNS', 'malignant CNS neoplasm', 'malignant central nervous system neoplasm', 'malignant CNS tumor', 'malignant CNS tumour', 'malignant tumour of CNS', 'CNS neoplasms, malignant', 'malignant tumor of central nervous system', 'malignant neoplasm of central nervous system', 'cancer of central nervous system', 'malignant tumour of the CNS', 'cancer of the central nervous system', 'malignant neoplasm of the central nervous system', 'malignant tumor of the central nervous system', 'central nervous system tumours', 'central nervous system tumors', 'central nervous system tumor', 'malignant tumor of CNS', 'central nervous system cancer', 'malignant CNS neoplasms', 'cancer of the CNS', 'CNS cancer', 'cancer of CNS', 'malignant tumour of central nervous system', 'central nervous system tumour', 'central nervous system neoplasms, malignant', 'malignant neoplasm of CNS']",3620,,,,"['0.1931', '-0.094', '-0.1317', '0.4702', '0.6616', '-0.8843', '0.4917', '0.597', '-0.11395', '0.01459', '0.4727', '0.2461', '-0.4065', '0.543', '-0.2869', '-0.174', '-0.2417', '-0.506', '-0.915', '-0.5356', '0.1929', '-0.6646', '-0.4395', '-0.1012', '0.1971', '-0.7456', '0.429', '0.1328', '0.456', '0.01704', '0.504', '-0.466', '0.1343', '-0.864', '0.7017', '-0.2974', '-1.109', '0.2418', '-0.3413', '-0.2708', '0.3037', '-0.1824', '0.2197', '0.1313', '-0.0662', '-0.01524', '-0.1941', '-0.868', '1.606', '-0.1964', '-0.05884', '-0.3342', '0.2559', '-0.21', '-0.4307', '0.2515', '-0.2644', '0.2664', '-1.138', '-0.9507', '0.434', '0.10583', '-0.3396', '-0.4133', '-0.4565', '0.6597', '0.385', '0.3552', '-0.11053', '0.8433', '0.11664', '0.915', '0.010635', '-0.3965', '1.203', '0.4192', '-0.04803', '0.12164', '-0.11633', '0.4675', '-0.1647', '0.3667', '-0.3306', '0.06885', '0.0879', '-0.1504', '0.843', '0.265', '0.856', '-0.4316', '0.03806', '0.0354', '-0.1329', '0.4841', '0.0427', '0.411', '-0.4395', '-0.9526', '-0.3884', '-0.0862']",C9293,0000326,D016543,239.7,,,
mondo:0002715,uterine cancer,"['CA - cancer of uterus', 'uterine cancer', 'tumor of uterus', 'uterus neoplasm', 'cancer of the uterus', 'malignant uterine neoplasm', 'uterine tumor', 'malignant uterus neoplasm', 'malignant tumor of the uterus', 'malignant uterine tumour', 'cancer of uterus', 'uterus cancer', 'malignant neoplasm of uterus', 'malignant tumour of the uterus', 'malignant uterine tumor', 'malignant tumor of uterus', 'uterine tumour', 'malignant tumour of uterus', 'malignant neoplasm of the uterus', 'neoplasm of uterus', 'tumour of uterus']",363,,,,,C3552,,D014594,179,,,
mondo:0002716,childhood spinal cord tumor,"['childhood spinal cord neoplasm', 'spinal cord neoplasm of childhood', 'pediatric spinal cord neoplasm', 'paediatric spinal cord neoplasm']",3637,,,C1134515,,C9234,,,,,,
mondo:0002717,spinal cord intramedullary teratoma,"['intramedullary teratoma of the spinal cord', 'intramedullary teratoma of spinal cord', 'intramedullary spinal cord teratoma', 'intramedullary spinal teratoma']",3639,,,C1334259,,C5428,,,,,,
mondo:0002718,central nervous system teratoma,"['teratoma of the central nervous system', 'teratoma of the CNS', 'central nervous system teratoma', 'teratoma of central nervous system', 'CNS teratoma', 'teratoma of CNS']",3640,,252018,C1332895,,C5441,,,,,,
mondo:0002719,conus medullaris neoplasm,"['tumour of conus medullaris', 'conus medullaris tumour', 'conus medullaris neoplasm', 'neoplasm of the conus medullaris', 'tumor of the conus medullaris', 'tumour of the conus medullaris', 'tumor of conus medullaris', 'conus medullaris tumor', 'conus medullaris neoplasm (disease)', 'neoplasm of conus medullaris']",3641,,,C1333153,,C5443,,,,,,
mondo:0002720,sella turcica neoplasm,"['sellar neoplasm', 'sella turcica tumor', 'sella turcica neoplasm', 'sella turcica tumour', 'neoplasm of the sella turcica', 'selt', 'tumor of the sella turcica', 'tumour of the sella turcica', 'sellar tumor', 'neoplasm of sella turcica', 'tumor of sella turcica', 'tumour of sella turcica', 'sellar tumour']",3643,,,C0748616,,C4944,,,,,,
mondo:0002721,necrosis of pituitary,"['pituitary necrosis', 'pituitary gland Necrosis']",3646,,,C0271558,,C27066,,,,,,
mondo:0002722,olfactory nerve neoplasm,"['olfactory nerve tumor', 'tumour of the first cranial nerve', 'first cranial nerve neoplasm', 'olfactory neural tumour', 'tumor of first cranial nerve', 'first cranial nerve tumour', 'neoplasm of first cranial nerve', 'tumor of olfactory nerve', 'neoplasms, cranial nerve I', 'first cranial nerve tumor', 'tumor of the first cranial nerve', 'tumour of olfactory nerve', 'neoplasm of the first cranial nerve', 'olfactory nerve neoplasms', 'tumour of the olfactory nerve', 'tumour of first cranial nerve', 'tumor of the olfactory nerve', 'neoplasms, olfactory nerve', 'neoplasm of the olfactory nerve', 'olfactory neural neoplasm', 'olfactory nerve neoplasm (disease)', 'olfactory neural tumor', 'neoplasm of olfactory nerve', 'cranial nerve I neoplasms', 'olfactory nerve tumour', 'olfactory nerve neoplasm', 'first cranial nerve neoplasms']",8256,,,C0346319,,C5121,,,239.7,,,
mondo:0002724,mast cell neoplasm,"['Mast cell tumor', 'mast cell tumor', 'mast cell neoplasm', 'Mast cell proliferative disease', 'mast cell tumour', 'neoplasm of the Mast cells', 'tumour of the Mast cells', 'Mast cell tumour', 'tumor of Mast cells', 'neoplasm of Mast cells', 'tumour of Mast cells', 'tumor of the Mast cells']",3664,,,C0334664,,C9295,0009000,,238.79,,,
mondo:0002726,cutaneous solitary mastocytoma,"['solitary mastocytoma of skin', 'solitary mastocytoma of the skin', 'skin solitary mastocytoma']",3666,,,,,C7138,1001844,D054705,,,,
mondo:0002727,olfactory nerve disorder,"['disorder of olfactory [1st] nerve', 'disorder of the 1st nerve', 'disorder of olfactory nerve', 'disease of olfactory nerve', 'olfactory nerve disease or disorder', 'olfactory nerve disorder', 'olfactory nerve disease', 'disorder of 1st nerve']",367,,,C0751937,,C27210,,D020431,352.0,,,
mondo:0002728,rhabdoid tumor,"['rhabdoid tumor', 'rhabdoid cancer', 'malignant rhabdoid tumor', 'rhabdoid sarcoma', 'malignant rhabdoid tumour']",3672,,69077,C0206743,,C3808,0005701,D018335,,,,
mondo:0002729,rhabdoid tumor of the kidney,"['kidney rhabdoid cancer', 'rhabdoid neoplasm of the kidney', 'rhabdoid tumour of the kidney (RTK)', 'malignant rhabdoid tumour of kidney', 'rhabdoid tumour of kidney', 'rhabdoid tumor of the kidney (RTK)', 'malignant rhabdoid tumor of the kidney', 'MRTK', 'renal rhabdoid tumour', 'kidney rhabdoid tumor', 'rhabdoid neoplasm of kidney', 'malignant rhabdoid tumour of the kidney', 'renal rhabdoid tumor', 'rhabdoid tumor of the kidney', 'malignant rhabdoid tumor of kidney', 'kidney rhabdoid tumour', 'renal rhabdoid neoplasm', 'rhabdoid tumor of kidney']",3674,,,C0854917,,C8715,1000512,,,,,
mondo:0002730,childhood kidney neoplasm,"['pediatric kidney neoplasm', 'childhood kidney tumour', 'kidney neoplasm of childhood', 'childhood renal tumor', 'childhood kidney tumor', 'childhood kidney neoplasm', 'pediatric kidney tumor', 'kidney neoplasm', 'pediatric renal tumor', 'childhood renal tumour', 'pediatric renal neoplasm', 'paediatric renal tumour', 'paediatric kidney tumour', 'paediatric renal neoplasm', 'paediatric kidney neoplasm', 'childhood renal neoplasm']",3675,,,C1333003,,C6563,,,,,,
mondo:0002731,cerebral hemisphere cancer,"['malignant cerebral hemispheric tumor', 'cancer of telencephalon', 'telencephalon cancer', 'malignant tumour of cerebrum', 'malignant cerebral hemisphere neoplasm', 'malignant cerebral hemispheric tumour', 'tumor of cerebrum', 'cerebrum cancer', 'malignant cerebral neoplasm', 'malignant tumour of cerebral hemispheres', 'malignant neoplasm of the cerebrum', 'malignant tumour of the cerebral hemispheres', 'malignant tumor of the cerebral hemispheres', 'cancer of cerebral hemisphere', 'malignant neoplasm of cerebral hemisphere', 'malignant neoplasm of cerebral hemispheres', 'malignant cerebral hemispheric neoplasm', 'malignant neoplasm of telencephalon', 'malignant cerebral tumour', 'malignant tumor of cerebrum', 'tumour of cerebrum', 'cerebral cancer', 'malignant tumour of the cerebrum', 'malignant tumor of the cerebrum', 'malignant cerebral tumor', 'malignant neoplasm of the cerebral hemispheres', 'malignant tumor of cerebral hemispheres', 'malignant neoplasm of cerebrum', 'malignant telencephalon neoplasm']",368,,,,,C4577,,,191.8,,,
mondo:0002732,lung benign neoplasm,"['tumour of the lung', 'benign tumor of lung', 'tumor of the lung', 'benign lung tumour', 'benign neoplasm of the lung', 'benign tumour of the lung', 'benign tumor of the lung', 'benign lung tumor', 'benign lung neoplasm', 'lung benign neoplasm', 'benign neoplasm of lung', 'benign tumour of lung']",3683,,,,,C4454,,,,,,
mondo:0002734,anal mucinous adenocarcinoma,"['mucinous adenocarcinoma of anus', 'anus mucinous adenocarcinoma', 'colloid adenocarcinoma of anus', 'mucinous adenocarcinoma of the anus', 'colloidal adenocarcinoma of the anus', 'anal mucinous adenocarcinoma', 'colloidal adenocarcinoma of anus', 'anal colloidal adenocarcinoma', 'colloid adenocarcinoma of the anus', 'anal colloid adenocarcinoma']",3691,,,C1332272,,C5606,,,,,,
mondo:0002735,anal canal adenocarcinoma,"['adenocarcinoma of anal canal', 'anal canal adenocarcinoma (disease)', 'adenocarcinoma arising in the anal mucosa', 'adenocarcinoma arising in anal mucosa', 'adenocarcinoma of the anal canal', 'anal canal adenocarcinoma']",3692,,424016,C1332259,,C7471,,,,,,0030439
mondo:0002736,ampulla of vater mucinous adenocarcinoma,"['ampulla of Vater mucinous adenocarcinoma', 'hepatopancreatic ampulla mucinous adenocarcinoma']",3693,,,C1332248,,C27416,,,,,,
mondo:0002737,acute sanguinous otitis media,,3696,,,C0395865,,,,,381.03,,,
mondo:0002738,acute transudative otitis media,"['acute non-suppurative otitis media', 'acute transudative otitis media', 'non-suppurative otitis media, acute', 'acute nonsuppurative otitis media', 'acute otitis media with effusion', 'acute secretory otitis media']",3697,,,C2939185,,,,,381.00,,,
mondo:0002739,extrahepatic bile duct mucinous adenocarcinoma,"['mucinous carcinoma of bile duct', 'colloidal adenocarcinoma of the bile duct', 'colloid adenocarcinoma of bile duct', 'colloid carcinoma of bile duct', 'colloidal adenocarcinoma of extrahepatic bile duct', 'colloid adenocarcinoma of the extrahepatic bile duct', 'colloid extrahepatic bile duct adenocarcinoma', 'colloid bile duct adenocarcinoma', 'colloidal extrahepatic bile duct adenocarcinoma', 'colloidal carcinoma of the bile duct', 'mucinous adenocarcinoma of bile duct', 'colloid adenocarcinoma of extrahepatic bile duct', 'mucinous adenocarcinoma of the extrahepatic bile duct', 'mucinous adenocarcinoma of extrahepatic bile duct', 'colloidal carcinoma of bile duct', 'extrahepatic bile duct mucinous adenocarcinoma', 'colloid carcinoma of the bile duct', 'mucinous adenocarcinoma of the bile duct', 'colloid bile duct carcinoma', 'bile duct colloid carcinoma', 'colloid adenocarcinoma of the bile duct', 'bile duct mucinous adenocarcinoma', 'mucinous extrahepatic bile duct adenocarcinoma', 'colloidal adenocarcinoma of the extrahepatic bile duct', 'colloidal bile duct carcinoma', 'mucinous bile duct adenocarcinoma', 'colloidal adenocarcinoma of bile duct', 'colloidal bile duct adenocarcinoma', 'mucinous carcinoma of the bile duct', 'bile duct colloidal carcinoma']",3698,,,C0861856,,C5846,,,,,,
mondo:0002740,uterine ligament mucinous adenocarcinoma,['uterine ligament mucinous adenocarcinoma'],3699,,,C1519869,,C40137,,,,,,
mondo:0002741,uterine ligament adenocarcinoma,['uterine ligament adenocarcinoma'],3700,,,C1519866,,C40135,,,,,,
mondo:0002742,cervical mucinous adenocarcinoma,"['cervical mucinous adenocarcinoma', 'uterine cervix mucinous adenocarcinoma']",3701,,,C1332919,,C36095,,,,,,
mondo:0002744,fallopian tube mucinous adenocarcinoma,['fallopian tube mucinous adenocarcinoma'],3704,,,C1517119,,C40103,,,,,,
mondo:0002745,fallopian tube mucinous tumor,"['fallopian tube mucinous tumor', 'fallopian tube mucinous neoplasm']",3705,,,C1517120,,C40109,,,,,,
mondo:0002746,fallopian tube adenocarcinoma,"['adenocarcinoma of the fallopian tube', 'adenocarcinoma of fallopian tube', 'fallopian tube adenocarcinoma']",3706,,,C1333590,,C6265,,,,,,
mondo:0002747,endometrial mucinous adenocarcinoma,"['endometrial mucinous adenocarcinoma', 'endometrium mucinous adenocarcinoma', 'uterine corpus mucinous adenocarcinoma', 'uterine mucinous carcinoma']",3707,,,C1519859,,C40144,1000236,,,,,
mondo:0002748,rectum mucinous adenocarcinoma,"['colloid adenocarcinoma of rectum', 'mucinous adenocarcinoma of the rectum', 'rectum mucinous adenocarcinoma', 'mucinous adenocarcinoma of rectum', 'rectal mucinous adenocarcinoma', 'colloidal adenocarcinoma of the rectum', 'colloidal adenocarcinoma of rectum', 'rectal colloidal adenocarcinoma', 'colloid adenocarcinoma of the rectum', 'rectal colloid adenocarcinoma']",3709,,,C0279652,,C7973,,,,,,
mondo:0002749,extracranial neuroblastoma,['extracranial neuroblastoma'],371,,,C1333499,,C5437,,,,,,
mondo:0002750,bladder colloid adenocarcinoma,['bladder mucinous adenocarcinoma'],3710,,,C1511193,,C39837,,,,,,
mondo:0002751,bladder adenocarcinoma,"['urinary bladder adenocarcinoma', 'adenocarcinoma of urinary bladder', 'adenocarcinoma of bladder', 'adenocarcinoma of the urinary bladder', 'bladder adenocarcinoma', 'blad', 'adenocarcinoma of the bladder']",3711,,,C0279682,,C4032,1000125,,,,,
mondo:0002752,ovarian adenocarcinoma,"['adenocarcinoma of ovary', 'ovarian adenocarcinoma', 'ovary adenocarcinoma', 'adenocarcinoma of the ovary']",3713,,213504,,,C7700,0006460,,,,10051938,
mondo:0002754,extramedullary plasmacytoma,"['plasmacytoma, extramedullary', 'plasmacytoma, extramedullary (not occurring in bone)', 'EP', 'extraosseous plasmacytoma', 'extramedullary plasmacytoma (clinical)', 'extramedullary plasmacytoma']",3720,,,C0278619,,C4002,,,203.80,C90.2,,
mondo:0002755,solitary osseous plasmacytoma,"['solitary plasmacytoma of bone', 'isolated osseous plasmacytoma', 'isolated plasmacytoma of bone', 'SPB']",3722,,,C0272256,,C7812,,,238.6,,,
mondo:0002756,solitary plasmacytoma of chest wall,"['chest wall solitary plasmacytoma', 'chest wall plasmacytoma', 'solitary plasmacytoma of chest wall', 'solitary plasmacytoma of the chest wall', 'plasmacytoma of chest wall']",3723,,,C1332936,,C6711,,,,,,
mondo:0002757,acute allergic sanguinous otitis media,,3728,,,C0155420,,,,,381.06,,,
mondo:0002758,vulva verrucous carcinoma,"['verrucous carcinoma of the vulva', 'verrucous carcinoma of vulva', 'vulvar verrucous carcinoma', 'mammalian vulva verrucous carcinoma']",3740,,,C1336983,,C6383,,,,,,
mondo:0002759,bladder verrucous carcinoma,"['bladder verrucous carcinoma', 'bladder verrucous squamous cell carcinoma', 'urinary bladder verrucous carcinoma']",3741,,,C1511208,,C39832,,,,,,
mondo:0002760,bladder squamous cell carcinoma,"['epidermoid carcinoma of urinary bladder', 'squamous cell carcinoma of bladder', 'squamous cell carcinoma of the bladder', 'epidermoid carcinoma of the bladder', 'urinary bladder epidermoid carcinoma', 'squamous cell carcinoma of urinary bladder', 'bladder squamous cell carcinoma', 'epidermoid carcinoma of bladder', 'bladder squamous cell cancer', 'epidermoid carcinoma of the urinary bladder', 'urinary bladder squamous cell carcinoma', 'bladder epidermoid carcinoma', 'BLSC', 'squamous cell carcinoma of the urinary bladder']",3742,,,C0279681,,C4031,1000130,,,,,
mondo:0002761,cervical verrucous carcinoma,"['cervical verrucous carcinoma', 'uterine cervix verrucous carcinoma']",3743,,,C1516435,,C40190,,,,,,
mondo:0002762,esophagus verrucous carcinoma,"['verrucous carcinoma of the esophagus', 'verrucous carcinoma of the oesophagus', 'verrucous carcinoma of oesophagus', 'esophagus verrucous carcinoma', 'esophageal verrucous cancer', 'verrucous carcinoma of esophagus', 'esophageal verrucous carcinoma']",3747,,,C1333470,,C27420,,,,,,
mondo:0002763,urethral verrucous carcinoma,"['urethral verrucous carcinoma', 'urethra verrucous carcinoma']",3749,,,C1519827,,C39874,,,,,,
mondo:0002764,urethra squamous cell carcinoma,"['urethral squamous cell cancer', 'urethra epidermoid carcinoma', 'urethral squamous cell carcinoma', 'urethra squamous cell carcinoma', 'squamous cell carcinoma of urethra', 'epidermoid carcinoma of the urethra', 'urethral epidermoid carcinoma', 'squamous cell carcinoma of the urethra', 'epidermoid carcinoma of urethra', 'USCC']",3750,,,C1336890,,C6165,,,,,,
mondo:0002765,plantar verrucous skin carcinoma,"['plantar part of pes verrucous carcinoma', 'plantar verrucous skin carcinoma', 'plantar verrucous carcinoma of the skin', 'plantar verrucous carcinoma of skin']",3751,,,C1335424,,C6811,,,,,,
mondo:0002766,larynx verrucous carcinoma,"['laryngeal throat verrucous cancer', 'larynx verrucous carcinoma', 'verrucous carcinoma of the larynx', 'verrucous carcinoma of larynx', 'laryngeal verrucous carcinoma']",3752,,,C0280328,,C8188,,,,,,
mondo:0002768,true hermaphroditism,"['ovotestis', 'hermaphroditism', 'true hermaphroditism']",3763,,,C0019269,,C85207,,,,,,
mondo:0002769,leukorrhea,"['leukorrhea of vagina', 'discharge - leukorrhea']",3766,,,,,,,D007973,,,,
mondo:0002770,vaginal discharge,"['Discharge, vaginal']",3767,,,,,C50795,,D019522,,,,
mondo:0002771,pulmonary fibrosis,"['fibrosis of lung', 'pulmonary interstitial fibrosis']",3770,,,C0034069,,C26869,,D011658,,,,
mondo:0002772,intraventricular meningioma,['brain ventricle meningioma (disease)'],3772,,,C1334271,,C5273,,,,,,
mondo:0002775,anovulation,,3781,,,C0003128,,,,D000858,,,,
mondo:0002776,external ear disorder,"['preauricular sinus or fistula', 'disease of external ear', 'external ear disorder', 'preauricular cyst', 'preauricular sinus or fistula NOS (disorder)', 'external ear disease', 'preauricular sinus and fistula', 'preauricular cyst (disorder)', 'disorder of external ear', 'external ear disease or disorder', 'preauricular sinus and fistula (disorder)']",379,,,C0155388,,C26972,,,744.47,H60-H62,,
mondo:0002778,epidural spinal canal meningioma,"['meningioma of epidural spinal canal', 'meningioma of the epidural spinal canal']",3809,,,C1333417,,C5310,,,,,,
mondo:0002779,central nervous system chondroma,"['chondroma of the central nervous system', 'central nervous system chondroma', 'osteochondroma of the central nervous system', 'osteochondroma of central nervous system', 'osteochondroma of the CNS', 'CNS osteochondroma', 'central nervous system osteochondroma', 'chondroma of the CNS', 'chondroma of CNS', 'chondroma of central nervous system', 'osteochondroma of CNS', 'CNS chondroma']",3813,,,C1333019,,C7001,,,,,,
mondo:0002781,glossopharyngeal nerve paralysis,"['glossopharyngeal nerve cranial nerve palsy', 'cranial nerve palsy of glossopharyngeal nerve']",3816,,,C0919940,,C27335,,,,,,
mondo:0002782,cranial nerve palsy,"['cranial nerve palsy', 'cranial nerve palsies', 'cranial nerve paralysis']",3817,,,C0151311,,C26941,,,,,,
mondo:0002783,Shwartzman phenomenon,"['Shwartzman reaction', 'Shwartzman reaction (function)']",3825,,,C0037018,,,,D012790,,,,
mondo:0002785,skull base neoplasm,"['tumours of skull base', 'tumor of the skull base', 'tumour of basicranium', 'basicranium tumor', 'tumour of skull base', 'tumour of the skull base', 'tumor of skull base', 'skull base tumour', 'neoplasm of skull base', 'skull base cancer', 'neoplasm of basicranium', 'tumor of basicranium', 'basicranium tumour', 'basicranium neoplasm (disease)', 'neoplasm of the skull base', 'skull base neoplasm', 'skull base tumor', 'tumors of skull base']",3842,,,C0376527,,C4676,,D019292,,,,
mondo:0002786,diencephalic cancer,"['malignant diencephalic tumour', 'tumor of diencephalon', 'tumour of diencephalon', 'diencephalon cancer', 'malignant diencephalic neoplasm', 'malignant diencephalic neoplasms', 'malignant neoplasm of diencephalon', 'cancer of diencephalon', 'malignant diencephalic tumor', 'malignant diencephalon neoplasm', 'diencephalic neoplasm']",3843,,,C1334576,,C5126,,,,,,
mondo:0002787,adamantinous craniopharyngioma,"['adamantinous Rathke^s pouch tumour', 'adamantinous neoplasm of Rathke^s pouch', 'adamantinous tumour of Rathke^s pouch', 'adamantinomatous craniopharyngioma', 'craniopharyngioma, adamantinomatous', 'adamantinous craniopharyngioma (morphologic abnormality)', 'adamantinous Rathke^s pouch neoplasm', 'adamantinous tumor of Rathke^s pouch', 'adamantinous Rathke^s pouch tumor']",3846,,,C0431129,,C4726,1000069,,,,,
mondo:0002788,papillary craniopharyngioma,"['papillary Rathke^s pouch tumour', 'papillary Rathke^s pouch neoplasm', 'craniopharyngioma, papillary', 'papillary tumor of Rathke^s pouch', 'papillary craniopharyngioma (morphologic abnormality)', 'craniopharyngioma, papillary (morphologic abnormality)', 'papillary Rathke pouch neoplasm', 'papillary Rathke^s pouch tumor', 'papillary tumour of Rathke^s pouch', 'papillary neoplasm of Rathke^s pouch']",3847,,,C0431128,,C4725,1000447,,,,,
mondo:0002789,hemangiopericytic tumor,['hemangiopericytic neoplasm'],3850,,,C0476144,,C7076,1000289,,,,,
mondo:0002790,seminal vesicle tumor,"['tumour of seminal vesicle', 'neoplasm of seminal vesicle', 'tumor of seminal vesicle', 'seminal vesicle neoplasm', 'seminal vesicle neoplasm (disease)', 'seminal vesicle tumor']",3855,,,C0341767,,C39908,,,239.5,,,
mondo:0002791,large cell medulloblastoma,"['large cell medulloblastoma (morphologic abnormality)', 'large cell medulloblastoma']",3857,,,C1266180,,C6904,0008508,,,,,
mondo:0002792,cerebellar vermis medulloblastoma,"['medulloblastoma of cerebellar vermis', 'medulloblastoma of the cerebellar vermis', 'cerebellar vermis medulloblastoma', 'vermis medulloblastoma']",3860,,,C1332903,,C5401,,,,,,
mondo:0002794,adult medulloblastoma,"['medulloblastoma', 'medulloblastoma of adults', 'adult brain medulloblastoma']",3864,,,C1332188,,C4011,,,,,,
mondo:0002795,adult central nervous system primitive neuroectodermal neoplasm,"['adult central nervous system primitive neuroectodermal tumour', 'adult central primitive neuroectodermal tumor', 'adult central primitive neuroectodermal tumour', 'adult CNS primitive neuroectodermal tumor', 'adult CNS PNET', 'adult central nervous system primitive neuroectodermal neoplasm', 'adult central nervous system primitive neuroectodermal tumor', 'adult CNS primitive neuroectodermal tumour', 'central nervous system primitive neuroectodermal neoplasm of adults', 'adult central primitive neuroectodermal neoplasm', 'adult CNS primitive neuroectodermal neoplasm']",3865,,,C1332196,,C5411,,,,,,
mondo:0002796,melanotic medulloblastoma,"['medulloblastoma, melanotic', 'melanotic medulloblastoma', 'medulloblastoma with melanotic differentiation', 'medulloblastoma, melanotic (morphologic abnormality)', 'MMBL', 'melanocytic medulloblastoma']",3868,,,C1275668,,C9497,,,,,,
mondo:0002797,childhood medulloblastoma,"['medulloblastoma, childhood', 'paediatric medulloblastoma', 'medulloblastoma', 'pediatric medulloblastoma', 'medulloblastoma of childhood', 'childhood medulloblastoma']",3869,,,C0278510,,C3997,,,,,,
mondo:0002798,childhood central nervous system primitive neuroectodermal neoplasm,"['paediatric central primitive neuroectodermal neoplasm', 'Central nervous system embryonal tumor, NOS', 'paediatric CNS primitive neuroectodermal neoplasm', 'childhood central nervous system primitive neuroectodermal tumor', 'paediatric CNS primitive neuroectodermal tumour', 'pediatric central primitive neuroectodermal neoplasm', 'pediatric central primitive neuroectodermal tumor', 'childhood CNS primitive neuroectodermal neoplasm', 'paediatric central nervous system primitive neuroectodermal neoplasm', 'pediatric central nervous system primitive neuroectodermal tumor', 'paediatric central primitive neuroectodermal tumour', 'childhood CNS primitive neuroectodermal tumour', 'childhood CNS PNET', 'pediatric central nervous system primitive neuroectodermal neoplasm', 'childhood central nervous system primitive neuroectodermal neoplasm', 'pediatric CNS primitive neuroectodermal neoplasm', 'childhood central primitive neuroectodermal tumor', 'pediatric CNS primitive neuroectodermal tumor', 'central nervous system primitive neuroectodermal neoplasm of childhood', 'childhood central nervous system primitive neuroectodermal tumour', 'childhood central primitive neuroectodermal tumour', 'childhood central primitive neuroectodermal neoplasm', 'paediatric CNS PNET', 'childhood central nervous system PNET', 'pediatric CNS PNET', 'paediatric central nervous system primitive neuroectodermal tumour', 'childhood CNS primitive neuroectodermal tumor']",3870,,,C1332957,,C5961,,,,,,
mondo:0002799,nodular medulloblastoma,,3873,,,C1334970,,C5407,,,,,,
mondo:0002800,thrombophlebitis,"['thrombophlebitis of a superficial leg vein', 'phlebitis and thrombophlebitis of superficial vessels of lower extremities', 'superficial thrombophlebitis of leg', 'thrombophlebitis of superficial veins of lower extremity']",3875,,,C0040046,,C3410,,D013924,451.2,I80.0,,
mondo:0002801,colonic pseudo-obstruction,"['acute colonic pseudo-obstruction', 'primary chronic pseudo-obstruction of colon', 'Ogilvie^s syndrome', 'ACPO', 'acute colonic ileus']",3876,,,C0009377,,,1000871,D003112,564.89,,,
mondo:0002802,functional colonic disease,,3877,,,C0009374,,,,D003109,,,,
mondo:0002803,intestinal pseudo-obstruction,"['intestine pseudoobstruction', 'hollow visceral myopathy', 'intestinal pseudoobstruction', 'intestinal pseudo-obstruction', 'pseudo-obstruction of intestine']",3878,,,,,C34733,1000988,D007418,569.89,,,
mondo:0002804,apocrine adenoma,['tubular apocrine adenoma'],3895,,,C0334345,,C4168,,,,,,
mondo:0002805,hidradenoma,"['hidradenoma', 'acrospiroma', 'eccrine acrospiroma', 'syringoadenoma', 'sweat gland adenoma', 'hidradenoma of skin']",3896,,,,,C7563,,,,,,
mondo:0002806,bronchogenic carcinoma,"['bronchus carcinoma', 'carcinoma, bronchial, malignant', 'bronchiogenic carcinoma', 'carcinoma of bronchus', 'bronchogenic lung cancer', 'bronchial carcinoma', 'bronchogenic lung carcinoma', 'BC - bronchogenic carcinoma', 'bronchogenic carcinoma']",3904,,,C0007121,,C35875,1001942,D002283,162.9,,,
mondo:0002807,bronchial neoplasm,"['bronchial neoplasm', 'neoplasm of bronchus', 'tumour of bronchus', 'bronchus neoplasm (disease)', 'bronchial neoplasm (disease)', 'bronchus tumor', 'bronchus tumour', 'tumor of bronchus', 'bronchus neoplasm']",3906,,,C0006264,,,1000849,D001984,,,,0030077
mondo:0002808,pancreatic serous cystadenoma,"['PSC', 'pancreatic microcystic adenoma', 'serous cystadenoma of pancreas', 'pancreatic serous cystadenoma', 'pancreas serous cystadenoma', 'serous cystadenoma of the pancreas']",3917,,,C1335316,,C5712,,,,,,
mondo:0002809,pancreatic cystadenoma,"['pancreatic cystadenoma', 'cystadenoma of pancreas', 'exocrine pancreas cystadenoma', 'cystadenoma of the pancreas']",3918,,,C0341486,,C4374,,,,,,
mondo:0002810,pancreatic serous cystic neoplasm,"['pancreatic serous neoplasm', 'pancreatic serous cystic neoplasm']",3919,,,C1518875,,C41248,,,,,,
mondo:0002811,main bronchus cancer,"['cancer of main bronchus', 'Ca main bronchus', 'main bronchus cancer', 'malignant main bronchus neoplasm', 'malignant neoplasm of main bronchus']",3924,,,C0153490,,,,,162.2,,,
mondo:0002812,infectious otitis interna,"['infectious otitis interna', 'inner Ear infection', 'internal Ear infection', 'infectious labyrinthitis', 'inner ear infection']",,,,C1168225,,C27339,,,,,,
mondo:0002813,lipomatous cancer,"['malignant lipomatous tumor', 'malignant tumour of the adipose tissue', 'malignant adipose tissue tumour', 'adipose tissue cancer', 'malignant tumor of adipose tissue', 'malignant lipomatous neoplasm', 'malignant tumour of adipose tissue', 'malignant tumor of the adipose tissue', 'malignant lipomatous tumour', 'malignant neoplasm of the adipose tissue', 'malignant adipose tissue tumor', 'malignant adipose tissue neoplasm', 'malignant neoplasm of adipose tissue', 'cancer of adipose tissue']",3939,,,C0346117,,C4501,,,171.9,,,
mondo:0002814,adrenal carcinoma,"['carcinoma of the adrenal gland', 'carcinoma of adrenal gland', 'adrenal gland carcinoma']",3950,,,,,,,,,,,
mondo:0002815,acute myocarditis,"['myocarditis, acute']",3951,,,C0155686,,C35206,,,422.99,,,
mondo:0002816,adrenal cortex disorder,"['adrenal cortex disease', 'disease of adrenal cortex', 'adrenal cortex disease or disorder', 'disorder of adrenal cortex']",3952,,,C0001614,,,,D000303,,,,
mondo:0002817,adrenal gland cancer,"['malignant tumour of the adrenal gland', 'malignant adrenal tumor', 'malignant adrenal neoplasm', 'adrenal neoplasm', 'malignant adrenal gland neoplasm', 'malignant adrenal tumour', 'malignant neoplasm of adrenal gland', 'adrenal gland cancer', 'malignant neoplasm of the adrenal gland', 'malignant tumor of adrenal gland', 'tumour of the adrenal gland', 'cancer of adrenal gland', 'malignant adrenal gland tumour', 'tumor of the adrenal gland', 'malignant adrenal gland tumor', 'malignant tumour of adrenal gland', 'adrenal cancer', 'malignant tumor of the adrenal gland']",3953,,,,,C9338,,D000310,239.7,,,
mondo:0002821,trabecular follicular adenocarcinoma,"['follicular adenocarcinoma, trabecular (morphologic abnormality)', 'trabecular follicular carcinoma', 'follicular adenocarcinoma, trabecular']",3964,,,C0334327,,,,,,,,
mondo:0002822,trabecular adenocarcinoma,"['trabecular adenocarcinoma', 'trabecular carcinoma', 'trabecular adenocarcinoma (morphologic abnormality)', 'Merkel cell carcinoma']",3965,,,C0302182,,C4068,,,,,,
mondo:0002824,extrinsic cardiomyopathy,['secondary cardiomyopathy'],3978,,,,,,,,425.8,,,
mondo:0002828,Bartholin gland transitional cell carcinoma,"['Bartholin gland transitional cell carcinoma', 'major vestibular gland transitional cell carcinoma', 'Bartholin^s gland transitional cell carcinoma']",3998,,,C1511053,,C40297,,,,,,
mondo:0002829,bartholin gland carcinoma,"['Bartholin gland carcinoma (disease)', 'major vestibular gland carcinoma', 'Bartholin gland cancer', 'bartholin gland carcinoma', 'carcinoma of Bartholin^s gland', 'Bartholin^s gland carcinoma', 'carcinoma of major vestibular gland', 'carcinoma of the Bartholin^s gland', 'Bartholin^s gland cancer']",60003,,,C0349561,,C9055,1000103,,,,,0030419
mondo:0002831,non-keratinizing sinonasal squamous cell carcinoma,"['non-keratinizing sinonasal squamous cell carcinoma', 'sinonasal squamous cell carcinoma', 'cylindrical cell carcinoma', 'Sinonasal transitional cell carcinoma', 'Schneiderian carcinoma', 'Ringertz carcinoma', 'Sinonasal cylindrical cell carcinoma', 'Sinonasal Schneiderian carcinoma']",4003,,,C0334270,,C54287,,,,,,
mondo:0002832,endometrial transitional cell carcinoma,['endometrial transitional cell carcinoma'],4005,,,C1516864,,C40154,,,,,,
mondo:0002833,fallopian tube transitional cell carcinoma,"['fallopian tube transitional cell carcinoma', 'fallopian tube transitional cell cancer']",4008,,,C1517128,,C40104,,,,,,
mondo:0002834,primary prostate urothelial carcinoma,"['primary prostate urothelial cancer', 'primary prostate urothelial carcinoma', 'prostate gland transitional cell carcinoma', 'transitional cell carcinoma of prostate', 'transitional cell carcinoma of the prostate', 'prostate urothelial carcinoma', 'prostate transitional cell carcinoma']",4011,,,C1514430,,C39898,,,,,,
mondo:0002836,urethra transitional cell carcinoma,"['urethra transitional cell carcinoma', 'urethral transitional cell carcinoma', 'urethral urothelial carcinoma', 'transitional cell carcinoma of urethra', 'UCU', 'urethral urothelial cancer', 'transitional cell carcinoma of the urethra']",4013,,,C0863015,,C6166,,,,,,
mondo:0002837,sarcomatoid transitional cell carcinoma,"['transitional cell carcinoma, sarcomatoid', 'sarcomatoid transitional cell carcinoma', 'transitional cell spindle cell carcinoma', 'transitional spindle cell carcinoma']",4014,,,C0334271,,C4120,,,,,,
mondo:0002839,leather-bottle stomach,"['linitis plastica', 'linitis plastica (morphologic abnormality)']",4023,,,C0023743,,C3190,,D008039,,,,
mondo:0002840,eosinophilic gastritis,['eosinophilic gastritis'],4030,,,C0267154,,C27052,,,535.70,,,
mondo:0002842,bacterial gastritis,"['Bacteria caused gastritis (disease)', 'bacterial gastritis']",4033,,,C0948039,,C27340,,,,,,
mondo:0002843,fungal gastritis,"['fungal gastritis', 'Fungi caused gastritis (disease)']",4034,,,C0948638,,C27342,,,,,,
mondo:0002844,lymphocytic gastritis,['lymphocytic gastritis'],4035,,,C1283271,,C27051,,,535.40,,,
mondo:0002845,necrotizing gastritis,['necrotizing gastritis'],4037,,,C0877152,,C27329,,,,,,
mondo:0002846,granulomatous gastritis,['granulomatous gastritis'],4038,,,C1112577,,C27348,,,,,,
mondo:0002847,skeletal muscle cancer,"['skeletal muscle tissue cancer', 'malignant skeletal muscle tumour', 'malignant tumor of skeletal muscle', 'malignant neoplasm of skeletal muscle tissue', 'malignant tumor of the skeletal muscle', 'malignant neoplasm of the skeletal muscle', 'malignant tumour of the skeletal muscle', 'malignant tumour of skeletal muscle', 'malignant skeletal muscle neoplasm', 'malignant skeletal muscle tissue neoplasm', 'cancer of skeletal muscle tissue', 'malignant neoplasm of skeletal muscle', 'malignant skeletal muscle tumor']",4043,,,C1334619,,C6516,,,,,,
mondo:0002848,skeletal muscle neoplasm,"['skeletal muscle neoplasm', 'neoplasm of skeletal muscle', 'tumour of skeletal muscle', 'tumour of the skeletal muscle', 'skeletal muscle tissue tumour', 'neoplasm of the skeletal muscle', 'tumor of skeletal muscle tissue', 'tumor of the skeletal muscle', 'neoplasm of skeletal muscle tissue', 'tumour of skeletal muscle tissue', 'skeletal muscle tissue tumor', 'skeletal muscle tumour', 'skeletal muscle tissue neoplasm (disease)', 'skeletal muscle tumor', 'tumor of skeletal muscle']",4044,,,C1335971,,C6514,,,239.2,,,
mondo:0002849,liver rhabdomyosarcoma,"['hepatic rhabdomyosarcoma', 'liver rhabdomyosarcoma (disease)', 'rhabdomyosarcoma of liver', 'liver rhabdomyosarcoma', 'rhabdomyosarcoma of the liver']",4047,,,C1333975,,C5834,,,,,,
mondo:0002850,central nervous system rhabdomyosarcoma,"['central nervous system rhabdomyosarcoma (disease)', 'rhabdomyosarcoma of the central nervous system', 'CNS rhabdomyosarcoma', 'rhabdomyosarcoma of CNS', 'rhabdomyosarcoma of the CNS', 'rhabdomyosarcoma of central nervous system', 'central nervous system rhabdomyosarcoma']",4048,,,C1332891,,C5464,,,,,,
mondo:0002851,mediastinum rhabdomyosarcoma,"['mediastinum rhabdomyosarcoma (disease)', 'rhabdomyosarcoma of mediastinum', 'rhabdomyosarcoma of the mediastinum', 'mediastinal rhabdomyosarcoma']",4049,,,C1334677,,C6617,,,,,,
mondo:0002852,mediastinum sarcoma,"['sarcoma of mediastinum', 'mediastinum sarcoma', 'mediastinal sarcoma', 'sarcoma of the mediastinum']",4050,,,C1334678,,C6606,,,,,,
mondo:0002853,rectum rhabdomyosarcoma,"['rectum rhabdomyosarcoma (disease)', 'rectal rhabdomyosarcoma', 'rhabdomyosarcoma of rectum', 'rhabdomyosarcoma of the rectum']",4053,,,C1335687,,C5627,,,,,,
mondo:0002854,prostate sarcoma,"['prostate gland sarcoma', 'sarcoma of prostate', 'prostate sarcoma', 'sarcoma of prostate gland', 'sarcoma of the prostate']",4054,,,C0238393,,C7731,,,,,,
mondo:0002855,ectomesenchymoma,"['malignant ectomesenchymoma', 'rhabdomyosarcoma with ganglionic differentiation', 'ectomesenchymoma', 'sarcoma with ganglionic or neuroectodermal differentiation', 'rhabdomyosarcoma with ganglionic differentiation (morphologic abnormality)']",4055,,,C0431111,,C4716,,,,,,
mondo:0002856,gallbladder rhabdomyosarcoma,"['rhabdomyosarcoma of the gallbladder', 'gall bladder rhabdomyosarcoma (disease)', 'gallbladder rhabdomyosarcoma', 'rhabdomyosarcoma of gallbladder']",4057,,,C1333756,,C5839,,,,,,
mondo:0002857,gallbladder sarcoma,"['malignant mesenchymal tumor of gallbladder', 'sarcoma of gall bladder', 'malignant mesenchymal tumour of gallbladder', 'sarcoma of the gallbladder', 'sarcoma of gallbladder', 'gall bladder sarcoma', 'gallbladder sarcoma']",4058,,,C1333757,,C5736,,,,,,
mondo:0002858,ovary rhabdomyosarcoma,"['ovary rhabdomyosarcoma (disease)', 'rhabdomyosarcoma of ovary', 'ovarian rhabdomyosarcoma', 'rhabdomyosarcoma of the ovary']",4059,,,C1335176,,C5236,,,,,,
mondo:0002859,breast rhabdomyosarcoma,"['breast rhabdomyosarcoma (disease)', 'breast rhabdomyosarcoma', 'rhabdomyosarcoma of the breast', 'rhabdomyosarcoma of breast']",4060,,,C1332637,,C5190,,,,,,
mondo:0002860,testis rhabdomyosarcoma,"['testicular rhabdomyosarcoma', 'rhabdomyosarcoma of testis', 'rhabdomyosarcoma of the testis', 'testis rhabdomyosarcoma (disease)']",4061,,,C1336726,,C6378,,,,,,
mondo:0002861,testis sarcoma,"['testis sarcoma', 'sarcoma of testis', 'testicular sarcoma', 'sarcoma of the testis']",4062,,,C1336727,,C6359,,,,,,
mondo:0002862,bile duct sarcoma,"['sarcoma of bile duct', 'bile duct sarcoma', 'sarcoma of the bile duct']",4064,,,C2205442,,C5029,,,,,,
mondo:0002863,rhabdomyosarcoma with mixed embryonal and alveolar features,"['mixed alveolar rhabdomyosarcoma', 'mixed embryonal rhabdomyosarcoma and alveolar rhabdomyosarcoma', 'mixed type rhabdomyosarcoma', 'mixed type alveolar rhabdomyosarcoma', 'rhabdomyosarcoma with mixed embryonal and alveolar features']",4065,,,C1709053,,C4259,,,,,,
mondo:0002864,anus rhabdomyosarcoma,"['anus rhabdomyosarcoma (disease)', 'anal rhabdomyosarcoma', 'rhabdomyosarcoma of the anus', 'rhabdomyosarcoma of anus']",4066,,,C1332276,,C5610,,,,,,
mondo:0002865,anus sarcoma,"['sarcoma of anus', 'anal sarcoma', 'anus sarcoma', 'sarcoma of the anus']",4067,,,C1332277,,C5611,,,,,,
mondo:0002866,duodenal disorder,"['duodenum disease', 'duodenum disease or disorder', 'disorder of duodenum', 'duodenum disorder', 'disease of duodenum']",4072,,,C0013289,,,,D004378,537.9,,,
mondo:0002867,pancreatic cystadenocarcinoma,"['cystadenocarcinoma of pancreas', 'cystadenocarcinoma of the pancreas', 'pancreas cystadenocarcinoma', 'cystadenocarcinoma - pancreas', 'pancreatic cystadenocarcinoma']",4073,,,C0238337,,C3874,,,,,,
mondo:0002868,bile duct mucinous cystic neoplasm with an associated invasive carcinoma,"['cystadenocarcinoma of the bile duct', 'cystadenocarcinoma of bile duct', 'biliary cystadenocarcinoma', 'bile duct cystadenocarcinoma', 'bile duct mucinous cystic neoplasm with an associated invasive carcinoma', 'bile duct cystadenocarcinoma (morphologic abnormality)']",4075,,,C0334286,,C4130,,,,,,
mondo:0002869,heart valve disorder,"['disorder of cardial valve', 'valvular heart disease', 'heart valve disorder', 'valvular heart disorder', 'disorder of heart valve', 'cardial valve disease or disorder', 'cardial valve disease', 'disease of cardial valve']",4079,,,C0018824,,C45525,,D006349,424.99,,,
mondo:0002870,tricuspid valve insufficiency,"['tricuspid regurgitation', 'tricuspid valve regurgitation', 'insufficiency, tricuspid', 'tricuspid insufficiency', 'tricuspid incompetence']",4080,,,C0040961,,C50842,,D014262,,,,
mondo:0002871,testicular trophoblastic tumor,['testicular trophoblastic tumor'],4084,,,C1515301,,C39934,,,,,,
mondo:0002872,trophoblastic neoplasm,"['neoplasm of trophoblast', 'trophoblast neoplasm (disease)', 'trophoblastic tumor', 'trophoblastic tumour', 'trophoblastic tumour (qualifier value)', 'trophoblastic neoplasm NOS (morphologic abnormality)', 'trophoblast tumour', 'trophoblastic neoplasms', 'trophoblastic tumor (qualifier value)', 'trophoblast tumor', 'tumour of trophoblast', 'trophoblastic neoplasm (morphologic abnormality)', 'trophoblastic neoplasm', 'tumor of trophoblast']",4085,,,C0041182,,C3422,,D014328,,,,
mondo:0002874,testicular pure germ cell tumor,"['testicular Pure germ cell tumour', 'testicular Pure germ cell tumor']",4087,,,C1514608,,C39915,,,,,,
mondo:0002875,parasitic ectoparasitic infectious disease,"['infestation, ectoparasitic', 'ectoparasitic infestation', 'Infestations, ectoparasitic', 'ectoparasitism']",4110,,,C0013578,,,,D004478,,B85-B89,,
mondo:0002876,cervical adenosarcoma,"['cervical Müllerian adenosarcoma', 'cervical adenosarcoma', 'adenosarcoma of the cervix uteri', 'uterine cervix adenosarcoma', 'cervical Muellerian adenosarcoma', 'cervical Mullerian adenosarcoma', 'adenosarcoma of uterine cervix']",4111,,213792,CN201069,,C40229,,,,C53.0,,
mondo:0002877,cervical carcinosarcoma,"['cervical malignant Müllerian mixed tumor', 'cervical malignant mixed mesodermal (Müllerian) tumor', 'cervical malignant mixed mesodermal (Mullerian) tumor', 'malignant Müllerian mixed tumor of the cervix uteri', 'cervical malignant mixed mesodermal mullerian tumor', 'cervical malignant Müllerian mixed tumour', 'cervical malignant mixed Mullerian tumour', 'malignant Mullerian mixed tumor of the cervix uteri', 'uterine cervix carcinosarcoma', 'cervical malignant Mullerian mixed tumor', 'cervical malignant Mullerian mixed tumour', 'cervical mixed epithelial and mesenchymal neoplasm', 'cervical malignant mixed mesodermal (Müllerian) tumour', 'cervical malignant mixed Mullerian tumor', 'malignant Mullerian mixed tumour of the cervix uteri', 'cervical carcinosarcoma', 'cervical malignant mixed mesodermal mullerian tumour', 'malignant Müllerian mixed tumour of the cervix uteri', 'cervical malignant mixed mesodermal (Mullerian) tumour', 'carcinosarcoma of the cervix uteri']",4112,,213787,CN201068,,C36097,,,,,,
mondo:0002878,uterine corpus adenosarcoma,"['adenosarcoma of the uterine corpus', 'uterine corpus Müllerian adenosarcoma', 'uterine corpus adenosarcoma', 'Mullerian adenosarcoma of the uterus', 'adenosarcoma of the corpus uteri', 'adenosarcoma of uterine body', 'uterine corpus Mullerian adenosarcoma', 'adenosarcoma of the body of uterus', 'adenosarcoma of the uterine body', 'adenosarcoma of body of uterus', 'adenosarcoma of uterine corpus', 'adenosarcoma of the uterus', 'uterine corpus mullerian adenosarcoma', 'body of uterus adenosarcoma', 'uterine adenosarcoma', 'uterine body adenosarcoma']",4113,,213600,CN201046,,C6336,,C538232,,,,
mondo:0002879,uterine body mixed cancer,"['malignant uterine body mixed neoplasm', 'malignant mixed tumor of the uterine body', 'malignant mixed neoplasm of the uterine corpus', 'malignant mixed tumour of the body of uterus', 'malignant corpus uteri mixed neoplasm', 'malignant mixed tumor of the body of uterus', 'malignant mixed neoplasm of uterine body', 'malignant body of uterus mixed tumor', 'malignant body of uterus mixed tumour', 'malignant mixed tumour of the corpus uteri', 'malignant mixed tumour of the uterine body', 'malignant mixed tumor of the uterine corpus', 'malignant mixed neoplasm of the uterine body', 'malignant mixed tumour of uterine body', 'malignant mixed neoplasm of the body of uterus', 'malignant mixed neoplasm of body of uterus', 'malignant mixed tumour of body of uterus', 'malignant mixed tumor of body of uterus', 'malignant corpus uteri mixed tumour', 'malignant mixed neoplasm of uterine corpus', 'malignant uterine body mixed tumor', 'malignant mixed neoplasm of the corpus uteri', 'malignant mixed tumour of corpus uteri', 'malignant mixed tumor of uterine corpus', 'malignant uterine body mixed tumour', 'malignant mixed tumor of corpus uteri', 'malignant mixed tumour of the uterine corpus', 'malignant corpus uteri mixed tumor', 'malignant body of uterus mixed neoplasm', 'malignant uterine corpus mixed tumour', 'malignant mixed tumour of uterine corpus', 'malignant uterine corpus mixed tumor', 'malignant mixed neoplasm of corpus uteri', 'malignant mixed tumor of uterine body', 'malignant uterine corpus mixed epithelial and mesenchymal neoplasm', 'malignant mixed tumor of the corpus uteri']",4114,,,C1334628,,C6311,,,,,,
mondo:0002880,ovarian adenosarcoma,"['ovarian mullerian adenosarcoma', 'ovarian Mullerian adenosarcoma', 'ovary adenosarcoma', 'ovarian Müllerian adenosarcoma', 'adenosarcoma of ovary', 'ovarian adenosarcoma', 'ovarian mesodermal adenosarcoma']",4115,,,C1335169,,C7317,,,,,,
mondo:0002881,vaginal adenosarcoma,"['vagina adenosarcoma', 'adenosarcoma of vagina', 'vaginal Müllerian adenosarcoma', 'vaginal adenosarcoma', 'vaginal Mullerian adenosarcoma']",4117,,,C1519914,,C40277,,,,,,
mondo:0002882,colon neuroendocrine neoplasm,"['neuroendocrine neoplasm of the colon', 'neuroendocrine tumor of the colon', 'colon neuroendocrine tumor', 'colon NET', 'colonic neuroendocrine tumour', 'colon neuroendocrine neoplasm', 'neuroendocrine tumour of the colon', 'colonic neuroendocrine neoplasm', 'colon neuroendocrine tumour', 'colon neuroendocrine tumor, well differentiated, low or intermediate grade', 'neuroendocrine neoplasm of colon', 'colonic neuroendocrine tumor']",4118,,100080,C1333097,,C5697,,,,,,
mondo:0002883,intestinal neuroendocrine neoplasm,"['intestine neuroendocrine neoplasm', 'neuroendocrine tumour of intestine', 'intestinal neuroendocrine benign tumour', 'intestine neuroendocrine tumor, well differentiated, low or intermediate grade', 'intestine NET', 'intestinal neuroendocrine neoplasm', 'intestinal neuroendocrine benign tumor', 'intestine neuroendocrine tumor', 'neuroendocrine tumor of intestine', 'intestine neuroendocrine tumour', 'neuroendocrine neoplasm of the intestine', 'neuroendocrine neoplasm of intestine']",4119,,,C1334231,,C5695,,,,,,
mondo:0002884,nail disorder,"['disease of nail', 'nail disease or disorder', 'disorder of nail', 'nail disease']",4123,,,C0027339,,,,D009260,703.9,,,
mondo:0002885,erythrasma,['infection due to Corynebacterium minutissimum'],4131,,,C2364003,,,1000696,D004894,041.85,L08.1,,
mondo:0002886,common bile duct disorder,"['common bile duct disease or disorder', 'disease of common bile duct', 'disorder of common bile duct', 'common bile duct disease']",4137,,,C0009440,,,,D003137,,,,
mondo:0002887,bile duct disorder,"['bile duct disorder', 'bile duct disease', 'disorder of bile duct', 'bile duct disease or disorder', 'disease of bile duct']",4138,,,C0005395,,C96716,,D001649,,,,
mondo:0002888,intraorbital meningioma,['intraorbital meningioma'],4141,,,C1334261,,C6778,,,,,,
mondo:0002889,orbital cancer,"['malignant orbital neoplasm', 'malignant tumour of orbit', 'malignant tumour of the orbit', 'orbital tumour', 'malignant tumor of orbit', 'malignant orbital tumour', 'neoplasm of orbit proper', 'malignant neoplasm of the orbit', 'malignant orbit tumor', 'malignant neoplasm of orbit of skull', 'orbit of skull cancer', 'malignant orbital tumor', 'malignant neoplasm of orbit', 'malignant orbit neoplasm', 'cancer of orbit of skull', 'orbit cancer', 'malignant orbit of skull neoplasm', 'malignant orbit tumour', 'orbital tumor', 'malignant tumor of the orbit']",4143,,,,,C3562,0007408,,239.89,,,
mondo:0002892,skull base chordoma,"['skull base chordoma', 'chordoma of skull base', 'chordoma of the skull base']",4151,,,C1335975,,C5453,,,,,,
mondo:0002894,spinal chordoma,"['spinal chordoma', 'spinal column chordoma', 'chordoma of the spinal column', 'chordoma of spine', 'spinal Chordomas', 'chordoma of spinal column']",4153,,,C1859101,,C5156,1000543,,,,,
mondo:0002896,primary syphilis,"['early symptomatic syphilis', 'early syphilis, symptomatic', 'symptomatic early syphilis']",4156,,,C2931317,,C128412,,C536772,091,,,
mondo:0002897,secondary syphilis,['secondary syphilis of viscera or bone'],4157,,,C0343676,,C128413,,C536773,091.9,,,
mondo:0002898,skin cancer,"['CA - skin cancer', 'malignant neoplasm of the skin', 'malignant neoplasm of skin', 'cancer of zone of skin', 'malignant skin tumor', 'skin cancer', 'malignant tumor of skin', 'malignant tumour of the skin', 'skin neoplasm, malignant', 'malignant zone of skin neoplasm', 'skin cancer, Including melanoma', 'cancer of skin', 'zone of skin cancer', 'melanoma and non-melanoma skin cancer', 'malignant tumor of the skin', 'malignant neoplasm of zone of skin', 'malignant skin tumour', 'malignant tumour of skin', 'malignant skin neoplasm']",4159,,,C0007114,,C2920,,,173.9,C43-C44,,
mondo:0002899,differentiating neuroblastoma,['differentiating neuroblastoma'],4160,,,C1511934,,C42048,,,,,,
mondo:0002900,cerebral neuroblastoma,"['neuroblastoma of cerebrum', 'neuroblastoma of brain', 'cerebral hemispheric neuroblastoma', 'neuroblastoma of cerebral hemispheres', 'neuroblastoma of the cerebral hemisphere', 'cerebral neuroblastoma', 'cerebral neuroblastoma, PNET', 'neuroblastoma of the cerebrum', 'telencephalon neuroblastoma', 'central nervous system neuroblastoma', 'neuroblastoma of telencephalon', 'neuroblastoma of the cerebral hemispheres']",4164,,,C0559458,,C4826,,,,,,
mondo:0002901,blood group incompatibility,,4176,,,C0005806,,,,,,,,
mondo:0002903,articulation disorder,"['phonological disorder', 'articulation impairment']",4186,,,,,C92564,,D001184,315.39,,,
mondo:0002904,echolalia,"['echolalia (disease)', 'echolalia']",4188,,,,,,,D004454,,,,0010529
mondo:0002905,mutism,"['mutism', 'mutism (disease)']",4189,,,C0026884,,,,D009155,,,,0002300
mondo:0002907,intracranial thrombosis,['cerebral thrombosis'],4193,,,C0752143,,,,D020767,434.00,,,
mondo:0002908,glucose metabolism disease,"['glucose metabolism disorder', 'disorder of glucose metabolism']",4194,,,C1257958,,C53655,,D044882,271.8,,,
mondo:0002909,hyperglycemia,,4195,,,C0020456,,,,D006943,790.6,,,
mondo:0002910,peroneal neuropathy,['peroneal neuropathy'],4201,,,C0747533,,C27596,,D020427,,,,
mondo:0002911,brain stem glioma,"['brainstem malignant glioma', 'brainstem glioma', 'brain stem glioma', 'brain stem neuroglial tumor', 'brain stem neuroglial tumour', 'diffuse brainstem glioma', 'malignant glioma of brainstem', 'glioma of the brain stem', 'brainstem neuroglial neoplasm', 'brainstem neuroglial tumour', 'glioma of brainstem', 'brain stem neuroglial neoplasm', 'glioma of brain stem', 'brainstem neuroglial tumor', 'glioma of the brainstem']",4202,,,C0677865,,C8501,,,,,,
mondo:0002912,brainstem cancer,"['malignant tumour of brain stem', 'malignant tumor of brain stem', 'malignant neoplasm of brainstem', 'primary brain stem tumor', 'malignant tumor of brainstem', 'malignant tumour of the brain stem', 'malignant brain stem tumour', 'malignant brainstem tumour', 'tumour of the brainstem', 'malignant tumour of the brainstem', 'neoplasm of brain stem', 'malignant tumour of brainstem', 'primary brain stem tumour', 'neoplasm of adult brain stem', 'malignant brain stem tumor', 'primary brain stem neoplasm', 'malignant neoplasm of brain stem', 'tumor of the brainstem', 'brain stem cancer', 'malignant neoplasm of the brainstem', 'malignant brainstem tumor', 'brainstem cancer', 'cancer of brainstem', 'malignant brain stem neoplasm', 'malignant tumor of the brainstem', 'malignant tumor of the brain stem', 'tumour of adult brainstem', 'malignant neoplasm of the brain stem', 'malignant brainstem neoplasm']",4203,,,C1332192,,C5967,,D020295,191.7,,,
mondo:0002913,cerebellar neoplasm,"['cerebellar tumour', 'malignant tumour of cerebellum', 'tumour of cerebellum', 'malignant tumor of cerebellum', 'cerebellum neoplasm (disease)', 'cerebellar tumor', 'neoplasm of the cerebellum', 'tumor of cerebellum', 'tumor of the cerebellum', 'cerebellum tumour', 'cerebellum tumor', 'cerebellar neoplasm', 'tumour of the cerebellum', 'neoplasm of cerebellum', 'cerebellum cancer']",4205,,,C0007762,,C2935,,D002528,191.6,,,
mondo:0002914,childhood brain stem neoplasm,"['childhood brain stem tumor', 'childhood tumor of brain stem', 'childhood tumor of the brain stem', 'pediatric brainstem cancer', 'childhood brainstem tumor', 'childhood tumour of brain stem', 'pediatric neoplasm of the brain stem', 'paediatric brain stem tumour', 'childhood neoplasm of brain stem', 'childhood brain stem neoplasm', 'childhood tumor of brainstem', 'childhood tumour of the brainstem', 'childhood tumour of brainstem', 'childhood neoplasm of brainstem', 'paediatric neoplasm of brain stem', 'paediatric brainstem tumour', 'childhood brain stem tumour', 'childhood tumour of the brain stem', 'pediatric tumor of brainstem', 'pediatric brain stem neoplasm', 'paediatric tumour of the brain stem', 'pediatric tumor of the brain stem', 'pediatric neoplasm of brain stem', 'pediatric brain stem tumor', 'childhood tumor of the brainstem', 'paediatric neoplasm of brainstem', 'pediatric brainstem tumor', 'pediatric neoplasm of brainstem', 'paediatric tumour of brainstem', 'pediatric neoplasm of the brainstem', 'brain stem neoplasm', 'paediatric neoplasm of the brainstem', 'paediatric tumour of the brainstem', 'paediatric brain stem neoplasm', 'brainstem cancer of childhood', 'pediatric brainstem neoplasm', 'childhood neoplasm of the brain stem', 'paediatric neoplasm of the brain stem', 'pediatric tumor of brain stem', 'paediatric brainstem cancer', 'childhood neoplasm of the brainstem', 'childhood brainstem neoplasm', 'pediatric tumor of the brainstem', 'childhood brainstem cancer', 'childhood brainstem tumour', 'paediatric tumour of brain stem', 'paediatric brainstem neoplasm']",4206,,,C1332951,,C5969,1001767,,,,,
mondo:0002915,childhood infratentorial neoplasm,"['paediatric infratentorial neoplasm', 'pediatric infratentorial tumor', 'paediatric infratentorial tumour', 'childhood infratentorial tumors', 'infratentorial neoplasm of childhood', 'childhood infratentorial tumor', 'childhood infratentorial neoplasms', 'pediatric infratentorial neoplasm', 'childhood infratentorial tumour', 'childhood infratentorial tumours', 'childhood infratentorial neoplasm']",4207,,,C1332973,,C5802,,,,,,
mondo:0002916,brainstem intraparenchymal clear cell meningioma,"['intraparenchymal clear cell meningioma of the brainstem', 'intraparenchymal clear cell meningioma of brainstem', 'brain stem intraparenchymal clear cell meningioma']",4209,,,C1332612,,C5295,,,,,,
mondo:0002917,disorder of pilosebaceous unit,"['hair disorder', 'disorder of pilosebaceous unit', 'pilosebaceous unit disease or disorder', 'hair and hair follicle diseases', 'pilosebaceous unit disease', 'hair disease', 'disease of pilosebaceous unit', 'hair/hair follicle diseases']",421,,,C0554472,,C34656,,D006201,704.9,,,
mondo:0002918,clear cell meningioma,"['clear cell meningioma (morphologic abnormality)', 'CCM', 'clear cell meningioma']",4210,,,C0431121,,C4722,1000180,,,,,
mondo:0002919,posterior cranial fossa meningioma,"['posterior cranial fossa meningioma (disease)', 'meningioma of the posterior cranial fossa', 'meningioma of posterior cranial fossa']",4211,,,C1335448,,C6775,,,,,,
mondo:0002920,malignant ovarian Brenner tumor,"['malignant Brenner tumor of ovary', 'malignant ovarian Brenner tumor', 'malignant Brenner tumor of the ovary', 'malignant Brenner tumour of the ovary', 'malignant Brenner tumour of ovary', 'ovarian Brenner tumor, malignant']",4217,,,C0334495,,C4270,1000357,,,,,
mondo:0002921,congenital structural myopathy,['centronuclear myopathy'],422,,,C0752282,,C84648,,D020914,,,,
mondo:0002922,pyoderma,,4223,,,C0034212,,,,D011711,686.09,L08.0,,
mondo:0002923,uterine corpus endometrial stromal sarcoma,"['endometrioid stromal sarcoma of body of uterus', 'body of uterus endometrioid stromal sarcoma', 'body of uterus endometrial stromal sarcoma', 'uterine corpus endometrial stromal sarcoma', 'uterine corpus ess', 'uterine corpus endometrial stromal tumour', 'uterine corpus endometrial stromal tumor']",4227,,,C1519849,,C40219,,,,,,
mondo:0002924,smooth muscle cancer,"['cancer of the smooth muscle', 'malignant tumour of smooth muscle', 'malignant tumor of smooth muscle', 'malignant smooth muscle tumour', 'malignant neoplasm of smooth muscle', 'malignant smooth muscle tumor', 'malignant tumour of the smooth muscle', 'malignant tumor of the smooth muscle', 'malignant smooth muscle neoplasm', 'smooth muscle cancer', 'cancer of smooth muscle', 'malignant neoplasm of the smooth muscle']",4230,,,C1334620,,C6511,,,,,,
mondo:0002926,clear cell sarcoma,"['clear cell sarcoma (morphologic abnormality)', 'malignant melanoma of soft parts', 'clear cell sarcoma of soft tissue', 'clear cell sarcoma - not kidney', 'clear cell sarcoma of soft parts', 'adult soft part clear cell sarcoma', 'malignant melanoma of the soft parts', 'malignant melanoma of soft tissues', 'melanoma, malignant, of soft parts', 'chordoid sarcoma', 'clear cell sarcoma/malignant melanoma of soft parts (excluding clear cell sarcoma of the kidney)']",4233,,,C0206651,,C3745,0008498,D018227,171.9,,,
mondo:0002927,spindle cell sarcoma,['spindle cell sarcoma'],4235,,,C0205945,,C27005,,,,,,
mondo:0002928,carcinosarcoma,"['mesodermal mixed tumour', 'mixed tumor, Mullerian', 'mixed mesodermal (mullerian) tumour', 'mixed Mullerian tumour', 'malignant mixed Mullerian tumor', 'mixed Mullerian tumor', 'carcinosarcoma, malignant', 'mesodermal mixed tumor (morphologic abnormality)', 'mixed mesodermal (mullerian) tumor', 'mullerian mixed tumor', 'mullerian mixed tumor (morphologic abnormality)', 'malignant mixed mesodermal (mullerian) tumour', 'mesodermal mixed tumor', 'mullerian mixed tumour (morphologic abnormality)', 'mesodermal mixed tumour (morphologic abnormality)', 'MMMT', 'malignant mixed mesodermal (mullerian) tumor', 'malignant mixed Mullerian tumour', 'carcinosarcoma', 'mullerian mixed tumour']",4236,,,C1334603,,C34448,,D002296,,,,
mondo:0002929,pulmonary immaturity,"['primary atelectasis, in perinatal period', 'primary atelectasis of newborn']",424,,,,,,,,770.4,,,
mondo:0002930,kidney sarcoma,"['kidney sarcoma', 'renal sarcoma', 'sarcoma of kidney', 'sarcoma of the kidney']",4242,,,C0346251,,C4525,,,189.0,,,
mondo:0002931,conjunctivochalasis,,4250,,,C0878693,,,,,372.81,,,
mondo:0002933,osteosclerosis,,4254,,,C0029464,,C41236,,D010026,,,,
mondo:0002934,intravascular angioleiomyoma,"['intravascular angiomyoma', 'intravascular angioleiomyoma']",4266,,,C1334267,,C5355,,,,,,
mondo:0002935,penis basal cell carcinoma,"['penile basal cell cancer', 'penis skin basal cell carcinoma', 'basal cell carcinoma of the penis', 'penile basal cell carcinoma', 'skin of penis skin basal cell carcinoma', 'skin basal cell carcinoma of penis']",4277,,,C1518949,,C39961,,,,,,
mondo:0002936,scrotum basal cell carcinoma,"['basal cell carcinoma of scrotum', 'basal cell scrotal carcinoma', 'scrotum skin basal cell carcinoma', 'basal cell carcinoma of the scrotum', 'scrotal basal cell carcinoma', 'skin basal cell carcinoma of scrotum']",4278,,,C1335934,,C6386,,,,,,
mondo:0002937,nodular basal cell carcinoma,"['basal cell carcinoma, nodular (morphologic abnormality)', 'skin nodulo-ulcerative basal cell carcinoma', 'Nodulo-ulcerative basal cell carcinoma', 'skin solid (nodular) basal cell carcinoma', 'circumscribed solid basal cell carcinoma', 'Rodent Ulcer', 'basal cell carcinoma, nodular']",4280,,,C1304300,,C5568,,,,,,
mondo:0002938,metatypical basal cell carcinoma,"['skin metatypical basal cell carcinoma', 'basosquamous carcinoma of skin', 'skin metatypical carcinoma']",4281,,,,,C66903,,,,,,
mondo:0002939,skin pigmented basal cell carcinoma,"['pigmented basal cell carcinoma', 'skin pigmented basal cell carcinoma']",4282,,,C1368275,,C9359,,,,,,
mondo:0002940,anal margin basal cell carcinoma,"['basal cell carcinoma of the anal margin', 'skin basal cell carcinoma of perianal skin', 'perianal skin skin basal cell carcinoma', 'anal margin basal cell carcinoma', 'perianal skin basal cell carcinoma', 'basal cell carcinoma of perianal skin', 'basal cell carcinoma of anal margin', 'basal cell carcinoma of the perianal skin']",4283,,,C1332269,,C7473,,,,,,
mondo:0002941,anal margin carcinoma,"['carcinoma of anal margin', 'carcinoma of the anal margin', 'perianal skin carcinoma', 'anal margin cancer', 'carcinoma of perianal skin', 'anal margin carcinoma']",4284,,,C0349534,,C7472,,,,,,
mondo:0002942,sebaceous basal cell carcinoma,['skin basosebaceous basal cell carcinoma'],4286,,,,,,,,,,,
mondo:0002943,external ear basal cell carcinoma,"['external Ear basal cell carcinoma', 'skin basal cell carcinoma of external ear', 'basal cell carcinoma of external ear', 'basal cell carcinoma of the external Ear', 'external ear skin basal cell carcinoma', 'basal cell carcinoma of external Ear', 'basal cell external ear carcinoma', 'basal cell carcinoma of the external ear']",4287,,,C1333491,,C6082,,,,,,
mondo:0002944,external ear carcinoma,"['carcinoma of external Ear', 'carcinoma of the external Ear', 'external Ear carcinoma', 'external ear carcinoma', 'carcinoma of external ear', 'carcinoma of the external ear']",4288,,,C1333492,,C6081,,,,,,
mondo:0002945,micronodular basal cell carcinoma,['skin micronodular basal cell carcinoma'],4289,,,C1367861,,C27541,,,,,,
mondo:0002946,gynatresia,,429,,,C0018414,,C84743,1001335,D006175,,,,
mondo:0002947,adamantinoid basal cell epithelioma,"['adamantinoid basal cell carcinoma', 'basal cell carcinoma - adamantinoid', 'skin adamantinoid basal cell carcinoma', 'melanotic adamantinoma of skin', 'skin adamantinoid basal cell epithelioma']",4290,,,C1304295,,C7585,,,,,,
mondo:0002948,skin fibroepithelial basal cell carcinoma,"['fibroepithelioma of Pinkus type', 'fibroepithelioma of Pinkus', 'Pinkus tumor', 'Pinkus tumour', 'fibroepithelial basal cell carcinoma']",4291,,,C0346013,,C4109,,,,,,
mondo:0002949,morpheaform basal cell carcinoma,"['morphea-type (sclerosing) basal cell carcinoma', 'basal cell carcinoma, morphea', 'basal cell carcinoma sclerosing type', 'morpheaform basal cell carcinoma', 'sclerosing type basal cell carcinoma', 'cicatricial basal-cell carcinoma', 'morphea-type basal cell carcinoma', 'skin morphea-type (sclerosing) basal cell carcinoma']",4292,,,C0555191,,C27182,,,,,,
mondo:0002950,skin clear cell basal cell carcinoma,"['clear cell basal cell carcinoma', 'skin clear cell basal cell carcinoma']",4293,,,C1516599,,C27536,,,,,,
mondo:0002951,skin adenoid basal cell carcinoma,"['adenoid basal cell carcinoma', 'skin adenoid basal cell carcinoma']",4294,,,,,C27535,,,,,,
mondo:0002952,follicular basal cell carcinoma,"['follicular (pilar) basal cell carcinoma', 'skin follicular basal cell carcinoma']",4295,,,C1883723,,C27538,,,,,,
mondo:0002953,skin infiltrative basal cell carcinoma,"['skin infiltrating basal cell carcinoma', 'infiltrative basal cell carcinoma', 'infiltrating basal cell carcinoma']",4299,,,C0334257,,C27539,,,,,,
mondo:0002954,superficial multifocal basal cell carcinoma,"['multifocal superficial basal cell carcinoma', 'superficial multicentric basal-cell carcinoma', 'superficial multifocal basal cell carcinoma', 'multifocal superficial basal cell carcinoma (morphologic abnormality)', 'superficial basal cell carcinoma', 'multicentric basal cell carcinoma']",4300,,,C0334256,,C4108,,,,,,
mondo:0002955,vulva basal cell carcinoma,"['mammalian vulva skin basal cell carcinoma', 'basal cell carcinoma of the vulva', 'skin basal cell carcinoma of mammalian vulva', 'vulvar basal cell carcinoma', 'vulvar basal cell cancer', 'basal cell carcinoma of vulva']",4301,,494451,C1336977,,C6381,,,,,,
mondo:0002956,skin cystic basal cell carcinoma,"['cystic basal cell carcinoma', 'skin cystic basal cell carcinoma']",4302,,,C1275193,,C27537,,,,,,
mondo:0002957,sarcomatoid basal cell carcinoma,['skin sarcomatoid basal cell carcinoma'],4303,,,C1519182,,C38111,,,,,,
mondo:0002958,signet ring basal cell carcinoma,"['skin signet Ring cell basal cell carcinoma', 'skin signet ring cell basal cell carcinoma', 'signet Ring cell basal cell carcinoma']",4304,,,C1519320,,C38110,,,,,,
mondo:0002959,radiculopathy,['nerve root disorder'],4306,,,C0700594,,,,D011843,,M54.1,,
mondo:0002960,polyradiculopathy,,4307,,,C0032586,,C34934,,D011128,356.9,,,
mondo:0002961,large cell acanthoma,,4321,,,C1334362,,C27518,,,,,,
mondo:0002962,epidermolytic acanthoma,,4323,,,C1333414,,C27516,,,,,,
mondo:0002963,acantholytic acanthoma,['acantholytic acanthoma'],4324,,,C1301270,,C27517,,,,,,
mondo:0002965,parovarian cyst,"['embryonic fimbrial cyst', 'Morgagni hydatid cyst', 'cysts, parovarian', 'hydatid of Morgagni', 'cysts, Paratubal', 'cyst, Paratubal', 'Paratubal cyst', 'cyst, fimbrial', 'Paratubal cysts', 'parovarian cysts', 'Morgagni hydatid cysts', 'cyst, parovarian', 'Morgagni Hydatids', 'Morgagni hydatid', 'hydatid cyst of Morgagni']",4333,,,C0030584,,,,D010310,,,,
mondo:0002966,splenic manifestation of prolymphocytic leukemia,"['prolymphocytic leukaemia of spleen', 'prolymphocytic leukemia of spleen', 'spleen prolymphocytic leukemia', 'spleen prolymphocytic leukaemia', 'splenic manifestation of prolymphocytic leukemia']",4334,,,C1336066,,C7297,,,,,,
mondo:0002967,dermatophytosis of scalp or beard,"['dermatophytosis of scalp', 'scalp dermatophytosis', 'dermatophytosis of scalp and beard', 'tinea capitis', 'Trichophyton rubrum tinea capitis', 'scalp ringworm', 'tinea capitis due to Trichophyton rubrum']",4337,,,C1274426,,C34536,,,110.0,,,
mondo:0002968,lymphocele,['lymph cyst'],4347,,,C0024248,,,,D008210,457.8,,,
mondo:0002969,ciliary body cancer,"['malignant tumour of the ciliary body', 'tumor of the ciliary body', 'malignant neoplasm of the ciliary body', 'malignant tumour of ciliary body', 'malignant tumor of the ciliary body', 'malignant tumor of ciliary body', 'tumour of the ciliary body', 'cancer of ciliary body', 'malignant neoplasm of ciliary body', 'malignant ciliary body neoplasm', 'malignant ciliary body tumour', 'ciliary body cancer', 'malignant ciliary body tumor']",4352,,,C0496833,,C4766,,,,,,
mondo:0002970,ciliary body disorder,"['ciliary body disease or disorder', 'ciliary body disorder', 'disease of ciliary body', 'ciliary body disease', 'disorder of ciliary body']",4353,,,C0271100,,C35775,,,,,,
mondo:0002971,amelanotic melanoma,"['amelanotic melanomas', 'amelanotic melanoma', 'melanomas, amelanotic', 'amelanotic melanoma (morphologic abnormality)', 'melanoma, amelanotic, malignant']",4359,,,C0206735,,C3802,1001937,D018328,,,,
mondo:0002972,posterior mediastinum cancer,"['malignant posterior mediastinum neoplasm', 'cancer of posterior mediastinum', 'malignant neoplasm of posterior mediastinum', 'posterior mediastinum cancer']",436,,,C0153502,,,,,164.3,,,
mondo:0002973,epithelioid cell melanoma,"['epithelioid cell malignant melanoma', 'epithelioid cell melanoma (morphologic abnormality)', 'epithelioid cell melanoma', 'epithelioid melanoma']",4360,,,C0334443,,C4236,,,,,,
mondo:0002974,cervical cancer,"['malignant tumor of the uterine cervix', 'cancer of uterine cervix', 'malignant cervical neoplasm', 'malignant tumour of uterine cervix', 'malignant cervix neoplasm', 'cervical cancer, somatic', 'malignant uterine cervix neoplasm', 'malignant neoplasm of the cervix uteri', 'malignant cervical tumour', 'malignant tumor of uterine cervix', 'malignant uterine cervix tumour', 'malignant tumor of the cervix uteri', 'tumor of the cervix uteri', 'cervix cancer', 'malignant cervix tumour', 'malignant uterine cervix tumor', 'malignant neoplasm of uterine cervix', 'malignant tumour of cervix', 'uterine cervical neoplasm', 'malignant cervical tumor', 'malignant neoplasm of cervix uteri', 'malignant tumour of the cervix', 'uterine cervix cancer', 'malignant neoplasm of cervix', 'malignant tumour of the cervix uteri', 'tumour of the cervix uteri', 'cervical neoplasm', 'malignant cervix tumor', 'malignant tumour of the uterine cervix', 'malignant tumor of the cervix', 'malignant neoplasm of the cervix', 'cervix uteri cancer', 'malignant tumor of cervix', 'malignant cervix uteri neoplasm', 'malignant tumour of cervix uteri', 'malignant cervix uteri tumour', 'malignant cervix uteri tumor', 'malignant neoplasm of the uterine cervix', 'malignant tumor of cervix uteri']",4362,603956,,,"['0.0234', '0.0595', '-0.002663', '-0.03027', '0.03558', '-0.0853', '0.02397', '0.0599', '-0.0703', '-0.03674', '-0.007454', '0.00864', '-0.01268', '0.01364', '-0.04736', '-0.04755', '-0.006237', '-0.05798', '-0.02374', '-0.10486', '-0.02316', '-0.00842', '0.02722', '-0.0411', '0.02768', '-0.009766', '0.02588', '0.01261', '0.006073', '-0.04715', '0.05682', '-0.00932', '0.0567', '-0.00607', '0.04608', '-0.015144', '-0.03403', '-0.04047', '-0.00114', '-0.05423', '0.012535', '-0.04364', '0.01842', '-0.03635', '0.00843', '-0.0329', '-0.0472', '0.04785', '0.0173', '0.0165', '-0.00724', '-0.00558', '0.02159', '0.02046', '-0.03214', '-0.01576', '0.04468', '-0.008606', '-0.0694', '-0.004425', '0.0819', '0.0166', '-0.01724', '0.01814', '-0.0322', '0.02779', '0.0725', '0.06088', '-0.04205', '0.0733', '-0.04297', '0.02145', '0.0313', '-0.04282', '0.03152', '0.011925', '-0.00122', '-0.01397', '-0.0409', '-0.063', '-0.04938', '0.0104', '-0.02101', '0.04053', '-0.04037', '-0.0142', '0.01605', '0.0457', '0.0847', '-0.02219', '-0.0241', '0.05942', '-0.01707', '0.01675', '0.1425', '0.0217', '0.04675', '-0.03882', '-0.02231', '0.008705']",C9311,,,180.9,,,
mondo:0002975,malignant breast melanoma,"['breast melanoma', 'malignant melanoma of the breast', 'malignant melanoma of breast', 'malignant breast melanoma', 'breast melanoma (disease)']",4364,,,C0346787,,C8410,,,,,,
mondo:0002976,stomach diverticulosis,,4370,,,C1148546,,,,D045724,,,,
mondo:0002977,autoimmune disorder of the nervous system,"['nervous system immune diseases', 'nervous system immune disorders', 'autoimmune disease of nervous system', 'autoimmune diseases, nervous system', 'disease, neurologic autoimmune', 'diseases, neurologic autoimmune', 'nervous system autoimmune diseases', 'autoimmune disease, neurologic', 'nervous system autoimmune disease', 'autoimmune disorders, nervous system', 'autoimmune disorders of the nervous system', 'autoimmune diseases, neurologic', 'nervous system hypersensitivity reaction type II disease', 'immune diseases, nervous system', 'immune disorders, nervous system', 'autoimmune nervous system diseases', 'neurologic autoimmune disease', 'autoimmune nervous system disorder', 'neurologic autoimmune diseases']",438,,,C0751872,,C99383,,D020274,,,,
mondo:0002978,orbit alveolar rhabdomyosarcoma,"['alveolar rhabdomyosarcoma of the orbit', 'alveolar rhabdomyosarcoma of orbit']",4384,,,C1335126,,C6247,,,,,,
mondo:0002979,papillary squamous carcinoma,"['papillary epidermoid carcinoma', 'papillary squamous carcinoma', 'papillary epidermoid cell carcinoma', 'papillary squamous cell carcinoma']",4385,,,C0334244,,C4102,,,,,,
mondo:0002981,peripheral primitive neuroectodermal tumor of bone,"['peripheral neuroectodermal tumor of the bone', 'peripheral neuroectodermal tumour of bone', 'osseous peripheral neuroepithelioma', 'peripheral primitive neuroectodermal tumor of bone', 'bone peripheral neuroepithelioma', 'peripheral primitive neuroectodermal tumour of bone tissue', 'peripheral primitive neuroectodermal tumor of bone tissue', 'peripheral neuroepithelioma of the bone', 'bone tissue peripheral primitive neuroectodermal tumor', 'peripheral neuroepithelioma of bone', 'peripheral neuroectodermal tumour of the bone', 'bone tissue peripheral primitive neuroectodermal tumour', 'peripheral neuroectodermal tumor of bone']",4388,,,C0855009,,C8776,,,,,,
mondo:0002982,peripheral primitive neuroectodermal tumor of soft tissues,"['peripheral primitive neuroectodermal tumor of soft tissues', 'peripheral neuroectodermal tumour of the soft tissues', 'peripheral neuroectodermal tumor of the soft tissues', 'peripheral neuroectodermal tumour of soft tissues', 'soft tissue peripheral neuroepithelioma', 'peripheral neuroepithelioma of soft tissues', 'peripheral neuroectodermal tumor of soft tissues', 'peripheral neuroepithelioma of the soft tissues']",4389,,,C1112437,,C27471,,,,,,
mondo:0002984,reticulohistiocytic granuloma,"['solitary reticulohistiocytoma', 'solitary histiocytoma', 'solitary reticulohistiocytosis', 'reticulohistiocytic granuloma (morphologic abnormality)', 'solitary Reticulohistiocytoma', 'Reticulohistiocytoma']",4394,,,C0035290,,C3356,,D015616,277.89,,,
mondo:0002987,spongiotic dermatitis,,4406,,,C0262984,,C27037,1000768,,692.9,,,
mondo:0002988,cervix melanoma,"['primary malignant melanoma of the cervix uteri', 'primary malignant melanoma of the uterine cervix', 'cervical melanoma', 'melanoma of the cervix']",4413,,,C0877611,,C40239,,,,,,
mondo:0002989,benign fibrous histiocytoma,"['fibrous histiocytoma NOS (morphologic abnormality)', 'benign fibrous histiocytoma (morphologic abnormality)', 'fibroxanthoma NOS (morphologic abnormality)', 'fibroxanthoma', 'fibrous histiocytoma', 'histiocytoma, fibrous, benign', 'benign fibrous histiocytoma']",4415,,,C0206644,,C3739,,D018219,,,,
mondo:0002990,benign deep fibrous histiocytoma,"['benign deep fibrous histiocytoma', 'deep benign fibrous histiocytoma']",4419,,,C1266125,,C6492,,,,,,
mondo:0002991,adenocarcinofibroma,"['adenofibroma, malignant', 'malignant adenofibroma', 'adenocarcinofibroma']",4422,,,C1510778,,C40035,,,,,,
mondo:0002993,pancreatic somatostatinoma,"['pancreatic somatostatin cell tumor', 'pancreatic delta cell somatostatin producing neoplasm', 'pancreatic somatostatin cell tumour']",4432,,,C1368041,,C95595,1001964,,,,,
mondo:0002994,pancreatic delta cell neuroendocrine tumor,"['pancreatic Delta cell neuroendocrine tumor', 'pancreatic Delta cell tumor', 'pancreatic Delta cell neuroendocrine tumour', 'pancreatic Delta cell tumour', 'pancreatic delta cell neoplasm', 'pancreatic Delta cell neoplasm', 'pancreatic Delta cell NET']",4433,,,C1335301,,C28396,,,,,,
mondo:0002995,"small intestine neuroendocrine tumor, well differentiated, low or intermediate grade","['small intestinal well differentiated endocrine tumour', 'small intestine neuroendocrine tumour', 'small intestinal neuroendocrine tumor', 'carcinoid tumour of small intestine', 'carcinoid tumor of small intestine', 'small intestinal well differentiated endocrine tumor/carcinoma', 'small intestinal well differentiated endocrine tumor', 'small intestine neuroendocrine tumor', 'small intestinal neuroendocrine tumour', 'small intestinal NET']",,,,C3272528,,C96061,1001928,,,,,
mondo:0002996,cavernous sinus meningioma,"['meningioma of the cavernous sinus', 'meningioma of cavernous sinus', 'cavernous sinus meningioma (disease)']",4435,,,C1332865,,C5268,,,,,,
mondo:0002997,anterior cranial fossa meningioma,"['meningioma of the anterior cranial fossa', 'anterior cranial fossa meningioma (disease)', 'anterior fossa meningioma', 'meningioma of anterior cranial fossa', 'meningioma of the anterior fossa', 'meningioma of anterior fossa']",4436,,,C1332301,,C5286,,,,,,
mondo:0002998,skull base meningioma,"['skull base meningioma', 'basicranium meningioma (disease)', 'meningioma of skull base', 'meningioma of the skull base']",4437,,,C1335976,,C5272,,,,,,
mondo:0002999,central nervous system germinoma,"['germinoma of the CNS', 'germinoma of central nervous system', 'germinoma of CNS', 'germinoma of the central nervous system', 'central nervous system germinoma', 'intracranial germinoma', 'central nervous system germinoma (disease)']",4438,,,,,C7009,,,,,,
mondo:0003000,central nervous system germ cell tumor,"['CNS germ cell tumor', 'central nervous system germ cell neoplasm', 'germ cell tumour of CNS', 'germ cell tumor of the central nervous system', 'germ cell tumour of central nervous system', 'germ cell tumor of the CNS', 'central nervous system germ cell tumor', 'central nervous system rare germ cell tumor', 'central nervous system rare germ cell tumour', 'germ cell tumor of central nervous system', 'germ cell neoplasm of the central nervous system', 'CNS germ cell tumour', 'germ cell neoplasm of CNS', 'germ cell neoplasm of central nervous system', 'CNS germ cell neoplasm', 'germ cell neoplasm of the CNS', 'germ cell tumour of the CNS', 'germ cell tumour of the central nervous system', 'germ cell tumor of CNS']",4439,,,C1332880,,C5461,,,,,,
mondo:0003001,seminoma,"['seminoma', 'seminoma, malignant', 'seminoma, pure']",4440,,,,,C9309,,D018239,186.9,,,
mondo:0003002,dysgerminoma,"['dysgerminoma (disease)', 'dysgerminoma, malignant', 'dysgerminoma']",4441,,,C0013377,,C2996,,D004407,,,,0100621
mondo:0003003,cervical alveolar soft part sarcoma,,4442,,,C1516408,,C40225,,,,,,
mondo:0003004,macular degeneration,"['macular degeneration of retina', 'retinal degeneration of macula lutea', 'macula lutea retinal degeneration', 'macula retinal degeneration']",4448,,,C0024437,,C123330,,D008268,,,,
mondo:0003005,macular retinal edema,"['retinal oedema of macula lutea', 'macula lutea retinal oedema', 'macular oedema', 'edema, macular', 'macular edema', 'macula lutea retinal edema', 'retinal edema of macula lutea']",4449,,,C0271051,,C35468,,,,,,
mondo:0003007,childhood kidney cell carcinoma,"['paediatric kidney cell carcinoma', 'pediatric kidney cell carcinoma', 'pediatric renal cell carcinoma (disease)', 'renal cell cancer', 'childhood renal cell carcinoma', 'paediatric renal cell carcinoma (disease)', 'renal cell carcinoma (disease) of childhood', 'pediatric renal cell carcinoma', 'childhood kidney cell carcinoma', 'paediatric renal cell carcinoma']",4454,,,C1333001,,C6568,,,,,,
mondo:0003008,hereditary renal cell carcinoma,"['hereditary renal cell carcinoma (disease)', 'hereditary renal cell carcinoma', 'familial renal carcinoma', 'hereditary renal cell cancer']",4455,,,,,C39789,,C536851,,,,
mondo:0003009,hyperaldosteronism,['primary hyperaldosteronism'],446,,,C0020428,,,,D006929,255.10,E26,,
mondo:0003010,multilocular clear cell renal cell carcinoma,"['multilocular clear cell renal cell carcinoma', 'multilocular clear cell renal cell adenocarcinoma', 'renal cystadenocarcinoma', 'cystadenocarcinoma of kidney', 'multilocular cystic renal neoplasm of low malignant potential', 'multilocular cystic renal cell adenocarcinoma', 'multilocular clear cell adenocarcinoma', 'multilocular cystic clear cell renal cell neoplasm of low malignant potential', 'multilocular cystic renal cell cancer', 'multilocular clear cell carcinoma', 'multilocular cystic renal cell carcinoma', 'MCRCC']",4463,,319287,C0346249,,C4524,,,189.0,,,
mondo:0003011,mucinous tubular and spindle renal cell carcinoma,"['renal mucinous tubular spindle cell carcinoma', 'mucinous tubular and spindle cell renal carcinoma', 'carcinoma, renal, tubular, malignant', 'mucinous tubular and spindle cell carcinoma of the kidney']",4472,,319322,CN203939,,C39807,,,,,,
mondo:0003012,sarcomatoid renal cell carcinoma,"['renal cell carcinoma, spindle cell', 'RCC w/ sarcomatoid features', 'renal cell carcinoma with sarcomatoid features', 'sarcomatoid renal cell cancer', 'SRCC', 'sarcomatoid renal cell carcinoma']",4473,,,C1266043,,C27893,,,,,,
mondo:0003014,rhinitis,"['nasal cavity mucosa inflammation', 'runny nose']",4483,,,C0035455,,C34986,0008521,D012220,,J30,,
mondo:0003017,malignant peritoneal solitary fibrous tumor,"['peritoneal solitary fibrous tumor, malignant', 'pleural and peritoneal solitary fibrous tumour', 'pleural and peritoneal solitary fibrous tumor']",4490,,,,,,,,,,,
mondo:0003019,potassium deficiency disease,"['hypokalemia', 'hypopotassemia', 'potassium deficiency disorder']",4500,,,C1514284,,C34939,,D007008,276.8,E87.6,,0002900
mondo:0003021,central nervous system angiosarcoma,"['angiosarcoma of the CNS', 'central nervous system angiosarcoma (disease)', 'central nervous system hemangiosarcoma', 'hemangiosarcoma of CNS', 'angiosarcoma of CNS', 'CNS hemangiosarcoma', 'angiosarcoma of central nervous system', 'central nervous system angiosarcoma', 'hemangiosarcoma of central nervous system', 'CNS angiosarcoma', 'angiosarcoma of the central nervous system', 'hemangiosarcoma of the CNS', 'hemangiosarcoma of the central nervous system']",4504,,,C1332875,,C5450,,,,,,
mondo:0003022,pediatric angiosarcoma,"['pediatric angiosarcoma', 'angiosarcoma', 'pediatric angiosarcoma (disease)', 'angiosarcoma (disease) of childhood', 'pediatric hemangiosarcoma', 'paediatric angiosarcoma (disease)', 'childhood angiosarcoma', 'childhood hemangiosarcoma', 'paediatric hemangiosarcoma']",4505,,,C0279988,,C9174,,,,,,
mondo:0003023,aorta angiosarcoma,"['aortic hemangiosarcoma', 'hemangiosarcoma of aorta', 'hemangiosarcoma of the aorta', 'aortic angiosarcoma', 'aorta angiosarcoma (disease)', 'angiosarcoma of aorta', 'angiosarcoma of the aorta']",4510,,,C1332312,,C5376,,,,,,
mondo:0003024,breast angiosarcoma,"['hemangiosarcoma of the breast', 'angiosarcoma of breast', 'BA', 'breast angiosarcoma', 'breast angiosarcoma (disease)', 'breast hemangiosarcoma', 'hemangiosarcoma of breast', 'angiosarcoma of the breast']",4511,,,C1332614,,C5184,,C536368,,,,
mondo:0003025,conventional angiosarcoma,['conventional angiosarcoma'],4512,,,C1333155,,C9426,,,,,,
mondo:0003026,gallbladder angiosarcoma,"['hemangiosarcoma of gallbladder', 'gall bladder angiosarcoma (disease)', 'hemangiosarcoma of the gallbladder', 'angiosarcoma of the gallbladder', 'gallbladder angiosarcoma', 'gallbladder hemangiosarcoma', 'angiosarcoma of gallbladder']",4513,,,C1333742,,C5840,,,,,,
mondo:0003027,thyroid gland angiosarcoma,"['hemangiosarcoma of the thyroid', 'thyroid hemangiosarcoma', 'angiosarcoma of the thyroid', 'angiosarcoma of the thyroid gland', 'hemangiosarcoma of the thyroid gland', 'hemangiosarcoma of thyroid', 'thyroid gland angiosarcoma', 'hemangiosarcoma of thyroid gland', 'angiosarcoma of thyroid', 'angiosarcoma of thyroid gland', 'thyroid gland angiosarcoma (disease)', 'thyroid gland hemangiosarcoma', 'thyroid angiosarcoma', 'thyroid gland malignant hemangioendothelioma']",4514,,,C1336748,,C6043,,,,,,
mondo:0003028,thyroid sarcoma,"['sarcoma of the thyroid gland', 'sarcoma of thyroid gland', 'sarcoma of thyroid', 'thyroid gland sarcoma', 'thyroid sarcoma', 'sarcoma of the thyroid']",4515,,,C1336756,,C6041,1001971,,,,,
mondo:0003029,skin angiosarcoma,"['skin hemangiosarcoma', 'angiosarcoma of the skin', 'hemangiosarcoma of the skin', 'hemangiosarcoma of skin', 'zone of skin angiosarcoma (disease)', 'skin angiosarcoma', 'angiosarcoma of skin']",4517,,,C0346081,,C4489,,,,,,
mondo:0003030,endometrioid stromal sarcoma of the cervix,"['uterine cervix endometrioid stromal sarcoma', 'cervical endometrial stromal sarcoma', 'endometrioid stromal sarcoma of the cervix', 'endometrial stromal sarcoma of the cervix', 'endometrioid stromal sarcoma of uterine cervix']",4520,,,C3642326,,C40220,,,,,,
mondo:0003031,endometrioid stromal and related neoplasms of the cervix,"['endometrioid stromal and related tumors of the cervix', 'endometrioid stromal and related neoplasms of the cervix', 'cervix endometrial stromal tumor', 'cervix endometrial stromal tumour', 'endometrioid stromal and related tumours of the cervix']",4521,,,C4289586,,C40218,,,,,,
mondo:0003032,superior vena cava angiosarcoma,"['anterior vena cava angiosarcoma (disease)', 'angiosarcoma of Superior vena cava', 'angiosarcoma of the Superior vena cava']",4522,,,C1336530,,C5378,,,,,,
mondo:0003033,prostate angiosarcoma,"['hemangiosarcoma of prostate', 'angiosarcoma of the prostate', 'hemangiosarcoma of the prostate', 'prostate gland angiosarcoma (disease)', 'prostate hemangiosarcoma', 'prostatic angiosarcoma', 'prostate angiosarcoma', 'angiosarcoma of prostate', 'prostatic hemangiosarcoma']",4524,,,C1335504,,C5528,,,,,,
mondo:0003034,mediastinum angiosarcoma,"['mediastinal hemangiosarcoma', 'hemangiosarcoma of the mediastinum', 'angiosarcoma of the mediastinum', 'mediastinal angiosarcoma', 'mediastinum angiosarcoma (disease)', 'hemangiosarcoma of mediastinum', 'angiosarcoma of mediastinum']",4525,,,C1334649,,C6613,,,,,,
mondo:0003035,ovarian angiosarcoma,"['hemangiosarcoma of the ovary', 'ovary angiosarcoma (disease)', 'angiosarcoma of ovary', 'ovarian hemangiosarcoma', 'hemangiosarcoma of ovary', 'angiosarcoma of the ovary']",4527,,,C1335152,,C5232,,,,,,
mondo:0003036,mucoepidermoid carcinoma,"['MEC', 'tumor, mucoepidermoid', 'mucoepidermoid tumours', 'mucoepidermoid tumour', 'mucoepidermoid carcinoma (morphologic abnormality)', 'mucoepidermoid tumors', 'mucoepidermoid tumor', 'tumors, mucoepidermoid', 'MUCC', 'mucoepidermoid carcinoma']",4531,,,C0206694,,C3772,1001049,D018298,,,,
mondo:0003037,hypotrichosis,,4535,,,,,C34720,,D007039,704.09,,,
mondo:0003038,dysgraphia,"['dysgraphia', 'dysgraphia (disease)']",4540,,,,,C182452,,,,,,0010526
mondo:0003039,nominal aphasia,"['anomic aphasia (finding)', 'anomic aphasia', 'anomia']",4541,,,,,,,D000849,,,,
mondo:0003040,retrograde amnesia,,4543,,,,,,,D000648,,R41.2,,
mondo:0003041,pediatric mesenchymal chondrosarcoma,"['pediatric mesenchymal chondrosarcoma', 'mesenchymal chondrosarcoma', 'mesenchymal chondrosarcoma of childhood', 'childhood mesenchymal chondrosarcoma']",4546,,,C1332982,,C27374,,,,,,
mondo:0003042,adult mesenchymal chondrosarcoma,"['mesenchymal chondrosarcoma of adults', 'adult mesenchymal chondrosarcoma']",4547,,,C1332207,,C27375,,,,,,
mondo:0003045,anal gland neoplasm,"['tumor of gland of anal canal', 'tumour of gland of anal canal', 'gland of anal canal neoplasm (disease)', 'neoplasm of gland of anal canal', 'gland of anal canal tumour', 'gland of anal canal tumor']",4550,,,C0002757,,,1000804,D000694,,,,
mondo:0003046,anus neoplasm,"['anus tumor', 'anal tumours', 'neoplasm of anus', 'tumor of the anus', 'anal neoplasms, benign and malignant', 'tumour of the anus', 'anal tumors', 'anus neoplasm', 'tumour of anus', 'neoplasm of the anus', 'anal tumor', 'anus neoplasm (disease)', 'anus tumour', 'tumor of anus', 'anal neoplasm', 'anal tumour']",4551,,,C0003463,,C2877,0003835,D001005,,,,
mondo:0003047,thymic large cell neuroendocrine carcinoma,"['large cell neuroendocrine carcinoma of the Thymus', 'thymic large cell neuroendocrine carcinoma', 'thymus large cell carcinoma', 'thymus large cell neuroendocrine carcinoma', 'large cell neuroendocrine carcinoma of Thymus', 'thymic LCNEC', 'Thymus large cell carcinoma', 'large cell carcinoma of the Thymus']",4553,,,C1334364,,C6461,,,,,,
mondo:0003049,ovarian large-cell neuroendocrine carcinoma,"['non-small-cell type neuroendocrine carcinoma of the ovary', 'large cell neuroendocrine carcinoma of ovary', 'large-cell neuroendocrine carcinoma of ovary', 'ovarian non-small-cell type neuroendocrine carcinoma', 'ovarian large cell neuroendocrine carcinoma', 'ovarian large cell NEC', 'ovary large cell neuroendocrine carcinoma', 'large-cell neuroendocrine carcinoma of the ovary', 'large cell neuroendocrine carcinoma of the ovary', 'non-small-cell type neuroendocrine carcinoma of ovary']",4555,,,C1335174,,C5238,,,,,,
mondo:0003050,lung large cell carcinoma,"['LCLC', 'large cell carcinoma of the lung', 'lung large cell carcinoma', 'anaplastic lung carcinoma', 'large cell lung cancer', 'large cell carcinoma of lung', 'large cell lung carcinoma', 'large cell undifferentiated lung carcinoma']",4556,,,C0345958,,C4450,1000016,,162.9,,,
mondo:0003051,non specific chronic endometritis,['non specific chronic endometritis'],4560,,,C1335061,,C27625,,,,,,
mondo:0003052,granulomatous endometritis,['granulomatous endometritis'],4561,,,C1333876,,C27626,,,,,,
mondo:0003053,choroid plexus meningioma,"['meningioma of the choroid plexus', 'choroid plexus meningioma (disease)', 'meningioma of choroid plexus', 'choroid plexus meningioma', 'choroid meningioma (morphologic abnormality)']",4584,,,C0431118,,C4719,,,,,,
mondo:0003054,benign meningioma,"['meningioma, benign', 'meningioma (disease), benign', 'benign meningioma (WHO grade I)']",4587,,,C0281784,,C4055,,,,,,
mondo:0003055,secretory meningioma,"['secretory meningioma (morphologic abnormality)', 'secretory meningioma']",4588,,,C1384406,,C4718,1000522,,,,,
mondo:0003056,lymphoplasmacyte-rich meningioma,"['lymphoplasmocyte-rich meningioma', 'lymphoplasmocyte-rich meningioma (morphologic abnormality)', 'lymphoplasmacyte-rich meningioma']",4591,,,C0431119,,C4720,1000342,,,,,
mondo:0003057,pediatric meningioma,"['childhood meningioma', 'pediatric meningioma (disease)', 'pediatric meningioma', 'meningioma (disease) of childhood', 'paediatric meningioma (disease)', 'meningioma']",4593,,,C0280656,,C8264,,,,,,
mondo:0003058,microcystic meningioma,"['microcystic meningioma (morphologic abnormality)', 'microcystic meningioma']",4594,,,C1384408,,C4721,1000376,,,,,
mondo:0003059,bile duct cancer,"['bile duct tumour', 'bile duct cancer', 'malignant neoplasm of bile duct', 'Ca extrahepatic bile ducts', 'malignant neoplasm of the extrahepatic bile duct', 'bile duct tumor', 'malignant bile duct neoplasm', 'cancer of bile duct']",4606,,,C0153453,,C7483,,,156.1,,,
mondo:0003060,biliary tract cancer,"['cancer of biliary tree', 'malignant tumor of biliary tract', 'malignant biliary tree neoplasm', 'biliary tree cancer', 'malignant neoplasm of biliary tree', 'malignant tumour of biliary tract']",4607,,,C0750952,,,,,156.9,,,
mondo:0003061,benign muscle neoplasm,"['benign muscle tumor', 'benign muscle tumour', 'benign neoplasm of muscle', 'benign muscle neoplasm', 'myomatous tumor', 'benign neoplasm of the muscle', 'benign tumor of muscle', 'benign tumour of the muscle', 'muscle benign neoplasm', 'benign tumor of the muscle', 'myoma', 'benign tumour of muscle', 'muscle tissue neoplasm', 'muscle neoplasm', 'myomatous tumour']",461,,,,,C4882,,D009214,,,,
mondo:0003062,intestinal benign neoplasm,"['benign intestine tumor', 'benign intestine tumour', 'benign intestine neoplasm', 'benign intestinal tumour', 'benign neoplasm of the intestines', 'benign neoplasm of intestines', 'intestine benign neoplasm', 'benign tumour of intestines', 'benign intestinal tumours', 'intestinal tumors, benign', 'benign neoplasms of the large and/or small intestine', 'intestinal neoplasms, benign', 'benign tumor of the intestines', 'benign neoplasms of large and/or small intestine', 'benign intestinal neoplasms', 'benign intestinal tumors', 'benign tumour of the intestines', 'benign intestinal tumor', 'benign tumor of intestines', 'benign intestinal neoplasm']",,,,C0347269,,C4609,,,,,,
mondo:0003064,inverted transitional cell papilloma,"['inverted transitional papilloma', 'transitional papilloma, inverted', 'inverted transitional cell papilloma']",4630,,,C0334269,,C4118,,,,,,
mondo:0003065,nasal cavity inverting papilloma,"['inverting papilloma of nasal cavity', 'nasal cavity Schneiderian papilloma, inverted type', 'nasal cavity inverted papilloma', 'inverting papilloma of the nasal cavity']",4633,,,C0280336,,C8194,,,,,,
mondo:0003066,submandibular adenitis,"['submandibular gland lymphadenitis (disease)', 'submandibular lymphadenitis']",4636,,,C0235591,,C27016,,,,,,
mondo:0003067,cervical lymphadenitis,"['cervical adenitis', 'neck lymphadenitis (disease)']",4637,,,C0149642,,C26937,,,,,,
mondo:0003068,postauricular lymphadenitis,['mastoid lymph node lymphadenitis (disease)'],4638,,,C0919638,,C27332,,,,,,
mondo:0003069,suppurative lymphadenitis,['suppurative lymphadenopathy'],4639,,,C0392051,,C27135,,,457.8,,,
mondo:0003070,axillary lymphadenitis,"['axilla lymphadenitis (disease)', 'axillary lymphadenitis', 'axillary adenitis']",4640,,,C0919797,,C27333,,,,,,
mondo:0003072,retinal cancer,"['malignant retina neoplasm', 'malignant tumour of the retina', 'malignant retinal tumor', 'retinal tumor', 'malignant neoplasm of the retina', 'malignant retina tumor', 'malignant retinal tumour', 'malignant tumor of retina', 'cancer of retina', 'malignant retina tumour', 'malignant neoplasm of retina', 'malignant tumour of retina', 'retinal tumour', 'malignant retinal neoplasm', 'retina cancer', 'malignant tumor of the retina']",4645,,,,,C3216,0005716,D019572,190.5,,,
mondo:0003073,trilateral retinoblastoma,,4647,,,C2608045,,C7019,,,,,,
mondo:0003075,bilateral retinoblastoma,,4650,,,C0854914,,C8713,,,,,,
mondo:0003076,unilateral retinoblastoma,,4651,,,C0854915,,C8714,,,,,,
mondo:0003077,intraocular retinoblastoma,['intraocular retinoblastoma'],4653,,,C0278717,,C7846,,,,,,
mondo:0003078,extraocular retinoblastoma,"['extraocular retinoblastoma', 'metastatic retinoblastoma']",4656,,,C0278719,,C7848,,,,,,
mondo:0003079,mastocytoma,['mastocytoma'],,,,C0024897,,C9303,,D034801,238.5,,,
mondo:0003081,thalamic disorder,"['dorsal plus ventral thalamus disease', 'disease of dorsal plus ventral thalamus', 'dorsal plus ventral thalamus disease or disorder', 'disorder of dorsal plus ventral thalamus']",4662,,,C0039726,,C85186,,D013786,,,,
mondo:0003082,filamentary keratitis,,4664,,,C0155077,,,,,370.23,,,
mondo:0003083,venous hemangioma,"['Venous angioma', 'Venous malformation']",467,,,C0334532,,C4296,,,228.09,,,
mondo:0003084,uremic neuropathy,,4675,,,C0268708,,C27055,,,357.4,,,
mondo:0003085,keratitis,['cornea inflammation'],4677,,,C0022568,,C26805,,D007634,370.9,H16,,
mondo:0003086,thymic mucoepidermoid carcinoma,"['thymic mucoepidermoid carcinoma', 'thymus mucoepidermoid carcinoma', 'Thymus mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the Thymus', 'mucoepidermoid carcinoma of Thymus']",4678,,,C1334814,,C6457,,,,,,
mondo:0003087,mucoepidermoid breast carcinoma,"['breast mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the breast', 'mucoepidermoid carcinoma of breast', 'mucoepidermoid breast carcinoma']",4679,,,C1334813,,C5166,,,,,,
mondo:0003088,intramuscular hemangioma,"['intramuscular angioma', 'intramuscular hemangioma (morphologic abnormality)']",468,,,C0205789,,C3699,,,,,,
mondo:0003089,extrahepatic bile duct mucoepidermoid carcinoma,"['mucoepidermoid carcinoma of bile duct', 'bile duct mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the bile duct', 'extrahepatic bile duct mucoepidermoid carcinoma']",4681,,,C1332552,,C5862,,,,,,
mondo:0003090,extrahepatic bile duct carcinoma,"['extrahepatic bile duct cancer', 'extrahepatic bile duct carcinoma', 'carcinoma of extrahepatic bile duct', 'carcinoma of the extrahepatic bile duct']",4682,,,C0238019,,C3860,,,,,,
mondo:0003091,cutaneous mucoepidermoid carcinoma,"['zone of skin mucoepidermoid carcinoma', 'mucoepidermoid skin carcinoma']",4683,,,C0346019,,C4472,,,,,,
mondo:0003092,lacrimal gland mucoepidermoid carcinoma,"['lacrimal gland mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the lacrimal gland', 'mucoepidermoid carcinoma of lacrimal gland']",4685,,,C1334359,,C6091,,,,,,
mondo:0003093,mucoepidermoid esophageal carcinoma,"['esophagus mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the oesophagus', 'oesophagus mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the esophagus']",4686,,,C1333461,,C5343,,,,,,
mondo:0003095,laryngeal mucoepidermoid carcinoma,"['mucoepidermoid carcinoma of the larynx', 'larynx mucoepidermoid carcinoma', 'laryngeal mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of larynx', 'laryngeal throat mucoepidermoid cancer']",4688,,,C1334373,,C9463,,,,,,
mondo:0003096,deep hemangioma,"['deep hemangioma', 'deep angioma']",469,,,C1333265,,C6555,,,,,,
mondo:0003097,childhood mediastinal neurogenic neoplasm,"['childhood mediastinal neurogenic tumour', 'pediatric neurogenic neoplasm of mediastinum', 'paediatric neurogenic tumour of mediastinum', 'childhood neurogenic tumor of the mediastinum', 'childhood neurogenic tumor of mediastinum', 'pediatric mediastinal neurogenic neoplasm', 'childhood mediastinal neurogenic tumor', 'paediatric neurogenic tumour of the mediastinum', 'paediatric neurogenic neoplasm of mediastinum', 'pediatric mediastinal neurogenic tumor', 'childhood neurogenic tumour of the mediastinum', 'pediatric neurogenic neoplasm of the mediastinum', 'childhood neurogenic neoplasm of mediastinum', 'childhood neurogenic tumour of mediastinum', 'paediatric mediastinal neurogenic neoplasm', 'childhood neurogenic neoplasm of the mediastinum', 'pediatric neurogenic tumor of the mediastinum', 'pediatric neurogenic tumor of mediastinum', 'childhood mediastinal neurogenic neoplasm', 'paediatric mediastinal neurogenic tumour', 'paediatric neurogenic neoplasm of the mediastinum']",4690,,,C1332981,,C5429,,,,,,
mondo:0003098,mediastinal neural neoplasm,"['neurogenic tumour of the mediastinum', 'neurogenic tumour of mediastinum', 'malignant mediastinal neurogenic neoplasm', 'mediastinal neural tumour', 'neurogenic neoplasm of the mediastinum', 'mediastinal neural neoplasm', 'mediastinal neurogenic tumour', 'mediastinal neurogenic tumor', 'neurogenic tumor of mediastinum', 'neurogenic neoplasm of mediastinum', 'neurogenic tumor of the mediastinum', 'mediastinal neural tumor', 'mediastinal neurogenic neoplasm']",4691,,,C1334672,,C6624,,,,,,
mondo:0003100,nerve plexus neoplasm,"['neural plexus tumors', 'tumor of the nerve plexus', 'nerve plexus tumors', 'nerve plexus neoplasm', 'nerve plexus neoplasms', 'nerve plexus tumour', 'nerve plexus tumor', 'tumor of nerve plexus', 'neoplasm of the nerve plexus', 'neural plexus tumours', 'tumour of nerve plexus', 'nerve plexus tumours', 'nerve plexus neoplasm (disease)', 'neural plexus neoplasms', 'tumour of the nerve plexus', 'neoplasm of nerve plexus']",4693,,,C1334945,,C5822,,,,,,
mondo:0003103,nerve root neoplasm,"['neoplasm of the nerve Root', 'tumour of nerve root', 'nerve Root tumours', 'nerve root tumour', 'neoplasms, nerve Root', 'neoplasm of nerve Root', 'tumor of the nerve Root', 'nerve root tumor', 'tumour of nerve Root', 'neoplasm of nerve root', 'tumour of the nerve Root', 'nerve Root tumour', 'nerve Root tumors', 'tumor of nerve Root', 'nerve Root tumor', 'nerve root neoplasm (disease)', 'nerve Root neoplasms', 'tumor of nerve root']",4698,,,C1334946,,C5119,,,,,,
mondo:0003104,epicardium cancer,"['epicardium cancer', 'epicardial tumour', 'malignant epicardial tumour', 'malignant neoplasm of epicardium', 'malignant tumor of the epicardium', 'malignant epicardium neoplasm', 'malignant tumor of epicardium', 'malignant tumour of epicardium', 'malignant epicardial tumor', 'epicardial tumor', 'cancer of epicardium', 'malignant neoplasm of the epicardium', 'malignant tumour of the epicardium', 'malignant epicardial neoplasm']",4699,,,C2607932,,C4568,,,,,,
mondo:0003105,prostate disorder,"['disease of prostate gland', 'prostate gland disease or disorder', 'prostate disorder', 'disorder of prostate gland', 'prostate disease', 'prostate gland disease']",47,,,C0033575,,C26865,,D011469,602.9,,,
mondo:0003107,infratentorial cancer,"['malignant infratentorial tumour', 'malignant infratentorial tumors', 'infratentorial neoplasms, malignant', 'brain neoplasm, infratentorial', 'malignant infratentorial tumor', 'malignant infratentorial tumours', 'malignant infratentorial neoplasm']",4706,,,C0751593,,C4966,,D015192,,,,
mondo:0003108,cervicomedullary junction neoplasm,"['neoplasm of cervicomedullary junction', 'neoplasm of the cervicomedullary junction', 'tumor of cervicomedullary junction', 'tumor of the cervicomedullary junction', 'cervicomedullary junction tumour', 'cervicomedullary junction neoplasms', 'cervicomedullary junction tumor', 'tumour of cervicomedullary junction', 'tumour of the cervicomedullary junction']",4707,,,C1332923,,C5423,,,,,,
mondo:0003109,foramen magnum meningioma,"['foramen magnum meningioma (disease)', 'meningioma of the Foramen magnum', 'meningioma of Foramen magnum']",4708,,,C1333630,,C5280,,,,,,
mondo:0003110,skin hemangioma,"['skin hemangioma', 'hemangioma of the skin', 'angioma of the skin', 'hemangioma of skin', 'angiomatous naevus of skin', 'hemangioma of zone of skin', 'zone of skin hemangioma', 'skin angioma', 'angioma of skin']",471,,,C0687140,,C4905,,,,,,
mondo:0003111,gastric neuroendocrine neoplasm,"['neuroendocrine tumor of stomach', 'neuroendocrine tumor of the stomach', 'neuroendocrine tumour of stomach', 'stomach neuroendocrine tumor', 'NET of stomach', 'stomach neuroendocrine neoplasm', 'stomach neuroendocrine tumor, well differentiated, low or intermediate grade', 'stomach neuroendocrine tumour', 'gastric neuroendocrine neoplasm', 'neuroendocrine neoplasm of the stomach', 'stomach NET', 'neuroendocrine tumour of the stomach', 'neuroendocrine neoplasm of stomach']",4715,,100075,C1333783,,C5696,,,,,,
mondo:0003112,malignant gastric germ cell tumor,"['germ cell tumour of the stomach', 'malignant germ cell tumour of stomach', 'malignant germ cell neoplasm of the stomach', 'malignant germ cell tumor of stomach', 'malignant germ cell tumor of the stomach', 'malignant gastric germ cell tumor', 'germ cell tumor of the stomach', 'malignant germ cell tumour of the stomach', 'malignant gastric germ cell neoplasm', 'malignant germ cell neoplasm of stomach']",4716,,,C1334584,,C5486,,,,,,
mondo:0003113,extragonadal germ cell cancer,"['extragonadal germ cell malignant tumor', 'malignant extragonadal germ cell tumour', 'tumor of extragonadal germ cell', 'tumour of extragonadal germ cell', 'extragonadal germ cell tumor, malignant', 'malignant tumour of extragonadal germ cell', 'malignant neoplasm of the extragonadal germ cell', 'malignant tumour of the extragonadal germ cell', 'malignant neoplasm of extragonadal germ cell', 'extragonadal germ cell malignant tumour', 'malignant tumor of the extragonadal germ cell', 'malignant tumor of extragonadal germ cell', 'malignant extragonadal germ cell tumor']",4717,,,C1334581,,C8881,,,,,,
mondo:0003115,subglottic hemangioma,"['subglottic hemangioma', 'hemangioma of subglottis', 'angioma of subglottis', 'hemangioma of the subglottis', 'subglottis angioma', 'subglottis hemangioma', 'angioma of the subglottis', 'subglottic angioma']",472,,,C1336518,,C6026,,,,,,
mondo:0003117,somatoform disorder,"['somatoform disorder', 'physiological malfunction arising from mental factor', 'psychophysiologic disorder', 'psychosomatic disorder']",4737,,,,,C34956,,D013001,306.8,,,
mondo:0003118,testicular Brenner tumor,"['testis Brenner tumor', 'testes, rudimentary Brenner tumor', 'testis Brenner tumour', 'testes, rudimentary Brenner tumour']",4739,,,C1515281,,C39953,,,,,,
mondo:0003120,mixed testicular germ cell cancer,"['testicular germ cell tumor (mixed)', 'testicular mixed germ cell tumor', 'mixed germ cell tumor of testis', 'testis mixed germ cell tumor', 'mixed testicular germ cell tumor', 'testicular mixed germ cell tumour', 'mixed germ cell tumour', 'mixed testicular germ cell tumour', 'mixed germ cell neoplasm of testis', 'mixed germ cell tumor', 'mixed germ cell tumor of the testis', 'testis mixed germ cell tumour', 'mixed germ cell tumour of testis', 'mixed germ cell tumour of the testis', 'testicular mixed germ cell neoplasm', 'mixed germ cell neoplasm of the testis', 'testicular germ cell tumour (mixed)']",4743,,,C1336720,,C6347,,,,,,
mondo:0003121,middle cranial fossa meningioma,"['meningioma of middle cranial fossa', 'meningioma of the middle cranial fossa', 'middle cranial fossa meningioma (disease)']",4749,,,C1334757,,C5586,,,,,,
mondo:0003122,striatonigral degeneration,,4751,,,C0270733,,C125695,,D020955,333.0,G23.2,,
mondo:0003124,testicular Leydig cell tumor,"['Leydig cell tumor of the testis', 'testis Leydig cell tumour', 'Leydig cell tumour of testis', 'Leydig cell neoplasm of testis', 'testicular Leydig cell neoplasm', 'testicular Leydig cell tumor', 'Leydig cell tumour of the testis', 'Leydig cell neoplasm of the testis', 'Leydig cell tumor of testis', 'testis Leydig cell tumor']",4756,,,C0863027,,C6356,1000569,,,,,
mondo:0003125,testicular sex cord-stromal neoplasm,"['testicular sex cord-stromal neoplasm', 'testis sex cord-stromal tumor', 'sex cord-stromal neoplasm of testis', 'sex cord-stromal tumour of the testis', 'testis sex cord-stromal tumour', 'sex cord-stromal tumor of the testis', 'sex cord-stromal tumour of testis', 'sex cord-stromal tumor of testis', 'testicular sex cord-stromal tumor', 'testicular sex cord-stromal tumour', 'sex cord-stromal neoplasm of the testis', 'sex cord-stromal neoplasm']",4757,,363489,CN204701,,C6358,,,,,,
mondo:0003126,breast hemangioma,"['angioma of the breast', 'breast angioma', 'hemangioma of the breast', 'hemangioma of breast', 'breast hemangioma', 'angioma of breast']",476,,,C0853715,,C5353,,,,,,
mondo:0003128,classic pulmonary blastoma,"['classic pulmonary blastoma', 'biphasic pulmonary blastoma']",4767,,,C1332556,,C36054,,,,,,
mondo:0003129,epithelial predominant pulmonary blastoma,['epithelial predominant pulmonary blastoma'],4768,,,C1333420,,C36053,,,,,,
mondo:0003130,mesoblastic nephroma,"['mesoblastic nephroma (morphologic abnormality)', 'mesoblastic nephroma']",4772,,,C0206628,,,,D018201,236.99,,,
mondo:0003133,exudative glomerulonephritis,,4777,,,C0546345,,C35706,,,,,,
mondo:0003134,proliferative glomerulonephritis,,4778,,,C0235618,,C35281,,,583.0,,,
mondo:0003135,focal embolic glomerulonephritis,,4779,,,C0238143,,C35707,,,,,,
mondo:0003136,anti-basement membrane glomerulonephritis,"['anti-GBM antibody disease', 'anti-glomerular basement Membrane antibody disease']",4780,,,C1332309,,C35798,,,,,,
mondo:0003137,diffuse glomerulonephritis,,4781,,,C0859036,,C35799,,,,,,
mondo:0003138,subacute glomerulonephritis,,4782,,,C1263744,,C35801,,,,,,
mondo:0003139,mesangial proliferative glomerulonephritis,"['glomerulonephritis - mesangial proliferative', 'mesangial proliferative GN', 'Mesangioproliferative glomerulonephritis']",4783,,,C0221238,,C35445,,,,,,
mondo:0003140,immune-complex glomerulonephritis,['immune Complex glomerulonephritis'],4784,,,C0744421,,C35800,,,583.89,,,
mondo:0003141,cerebellopontine angle embryonal tumor,"['C-P angle primitive neuroectodermal tumour', 'primitive neuroectodermal neoplasm of cerebellar Pontine angle', 'primitive neuroectodermal neoplasm of the cerebellar Pontine angle', 'cerebellar Pontine angle primitive neuroectodermal neoplasm', 'primitive neuroectodermal tumour of the C-P angle', 'cerebellopontine angle primitive neuroectodermal neoplasm', 'primitive neuroectodermal tumor of the cerebellopontine angle', 'cerebellar Pontine angle primitive neuroectodermal tumor', 'primitive neuroectodermal tumour of the cerebellar Pontine angle', 'primitive neuroectodermal neoplasm of cerebellopontine angle', 'primitive neuroectodermal tumor of the cerebellar Pontine angle', 'primitive neuroectodermal tumor of cerebellopontine angle', 'primitive neuroectodermal tumor of the C-P angle', 'cerebellar Pontine angle PNET', 'primitive neuroectodermal neoplasm of the C-P angle', 'cerebellopontine angle primitive neuroectodermal', 'cerebellopontine angle PNET', 'primitive neuroectodermal tumour of cerebellopontine angle', 'primitive neuroectodermal tumour of cerebellar Pontine angle', 'cerebellopontine angle primitive neuroectodermal tumor', 'primitive neuroectodermal tumor of cerebellar Pontine angle', 'primitive neuroectodermal neoplasm of C-P angle', 'primitive neuroectodermal tumor of C-P angle', 'C-P angle primitive neuroectodermal neoplasm', 'C-P angle primitive neuroectodermal tumor', 'C-P angle PNET', 'cerebellopontine angle primitive neuroectodermal tumour', 'primitive neuroectodermal tumour of C-P angle', 'primitive neuroectodermal neoplasm of the cerebellopontine angle', 'primitive neuroectodermal tumour of the cerebellopontine angle', 'cerebellar Pontine angle primitive neuroectodermal tumour']",4787,,,C1332904,,C5436,,,,,,
mondo:0003142,intracranial primitive neuroectodermal tumor,"['intracranial PNET', 'intracranial primitive neuroectodermal neoplasm', 'primitive neuroectodermal tumour of brain', 'primitive neuroectodermal tumor of brain', 'brain primitive neuroectodermal tumour', 'intracranial primitive neuroectodermal tumor', 'brain primitive neuroectodermal tumor']",4788,,,C1334246,,C5817,,,,,,
mondo:0003143,angiokeratoma,"['skin angiokeratoma', 'angiokeratoma of skin', 'cutaneous angiokeratoma', 'angiokeratoma of the skin', 'angiokeratoma (morphologic abnormality)']",479,,,C0346075,,C4488,,D000794,,,,
mondo:0003144,medulloepithelioma,"['medulloepithelioma, central nervous system', 'Diktyoma, malignant', 'central nervous system medulloepithelioma', 'MDEP', 'medulloepithelioma of the central nervous system', 'medulloepithelioma NOS (morphologic abnormality)']",4790,,251883,C0334596,,C4327,,,,,,
mondo:0003145,supratentorial primitive neuroectodermal tumor,"['CNS/supratentorial PNET', 'supratent. primitive neuro. tumour', 'supratentorial PNET', 'supratent. primitive neuro. tumor', 'supratentorial primitive neuroectodermal tumor']",4791,,,C1336538,,C6968,,,209.30,,,
mondo:0003147,space motion sickness,"['motion sickness, Space', 'syndrome, Space adaptation', 'adaptation syndrome, Space', 'Space adaptation syndrome']",4796,,,C0242700,,,1001188,D018489,,,,
mondo:0003150,male reproductive system disorder,"['disorder of male reproductive system', 'disorder of Male reproductive system', 'male reproductive disease', 'Male reproductive system disease', 'disease of male reproductive system', 'male reproductive system disease', 'male reproductive system disease or disorder', 'Male reproductive system disorder']",48,,,,,C27019,,D005832,608.9,N40-N53,,
mondo:0003152,adult brainstem gliosarcoma,"['adult brain stem gliosarcoma', 'adult brainstem gliosarcoma']",4812,,,C1377914,,C9370,,,,,,
mondo:0003153,adult brainstem glioma,"['brain stem glioma', 'adult brain stem glioma', 'brain stem glioma of adults', 'adult brainstem neuroglial neoplasm', 'adult brainstem neuroglial tumor', 'adult brainstem glioma', 'adult brainstem neuroglial tumour', 'glioma of the adult brain stem', 'glioma of adult brain stem']",4813,,,C0278873,,C9091,,,,,,
mondo:0003154,hemangioma of peripheral nerve,"['nerve hemangioma', 'hemangioma of nerve', 'hemangioma of peripheral nerve']",482,,,C1333956,,C27507,,,,,,
mondo:0003155,cavernous hemangioma,"['cavernous haemangioma', 'cavernoma', 'cavernous angioma', 'cavernous hemangioma', 'cavernous hemangioma (morphologic abnormality)']",483,,,C0018920,,C3086,1000151,D006392,,,,0001048
mondo:0003157,disappearing bone disease,"['essential osteolysis', 'phantom bone disease', 'massive osteolysis', 'Gorham^s disease', 'Gorham-Stout syndrome']",4837,,,C0029436,,,,,733.09,,,
mondo:0003158,malignant myoepithelioma,"['malignant myoepithelioma', 'myoepithelioma, malignant', 'soft tissue myoepithelial carcinoma', 'myoepithelioma carcinoma', 'myoepithelial carcinoma']",4838,,,C0334699,,C7596,,,,,,
mondo:0003159,vascular hemostatic disease,"['vascular hemostatic disorder', 'hemostatic disorder', 'disorders, vascular hemostatic', 'hemostatic disorder, vascular', 'hemostatic disorders, vascular', 'disorder, vascular hemostatic', 'vascular hemostatic disorders']",484,,,C0600502,,,,D020141,,,,
mondo:0003163,cauda equina intradural extramedullary astrocytoma,"['intradural extramedullary Cauda equina astrocytoma', 'intradural extramedullary astrocytic tumour of the Cauda equina', 'intradural extramedullary astrocytic tumor of the Cauda equina', 'intradural extramedullary astrocytoma of the Cauda equina', 'intradural extramedullary astrocytoma of Cauda equina']",4846,,,C1334254,,C5408,,,,,,
mondo:0003164,cauda equina neoplasm,"['Cauda equina neoplasms', 'tumor of cauda equina', 'cauda equina neoplasm (disease)', 'tumour of Cauda equina', 'tumor of the Cauda equina', 'tumour of cauda equina', 'cauda equina tumor', 'cauda equina tumour', 'neoplasm of cauda equina', 'tumor of Cauda equina', 'tumour of the Cauda equina', 'neoplasm of the Cauda equina']",4847,,,C1263892,,C5479,,,,,,
mondo:0003165,cerebellar astrocytoma,"['astrocytoma, cerebellar', 'astrocytoma of the cerebellum', 'astrocytoma (excluding glioblastoma) of cerebellum', 'astrocytoma of cerebellum', 'cerebellum astrocytoma', 'cerebellar astrocytoma', 'cerebellum astrocytoma (excluding glioblastoma)']",4848,,,C0740480,,C9475,,,,,,
mondo:0003168,cerebellar pilocytic astrocytoma,"['pilocytic astrocytoma of cerebellum', 'cerebellar pilocytic astrocytoma', 'pilocytic astrocytoma of the cerebellum', 'cerebellum pilocytic astrocytoma']",4853,,,C0349620,,C6809,,,,,,
mondo:0003169,diencephalic astrocytomas,"['diencephalon astrocytoma (excluding glioblastoma)', 'diencephalic astrocytoma', 'astrocytoma of diencephalon', 'astrocytoma (excluding glioblastoma) of diencephalon', 'diencephalon astrocytoma', 'astrocytoma of the diencephalon']",4855,,,C1333284,,C5128,,,,,,
mondo:0003170,gliofibroma,['gliofibroma (morphologic abnormality)'],4856,,,C1266178,,C5419,,,,,,
mondo:0003171,pineal gland astrocytoma,"['pineal astrocytoma', 'pineal astrocytic tumour', 'astrocytoma (excluding glioblastoma) of pineal body', 'pineal body astrocytoma', 'pineal astrocytic tumor', 'pineal body astrocytoma (excluding glioblastoma)', 'astrocytoma of pineal gland', 'astrocytoma of the pineal gland']",4858,,,C0280795,,C8274,,,,,,
mondo:0003172,glomeruloid hemangioma,,486,,,C1304511,,C27505,,,,,,
mondo:0003173,brain stem astrocytic neoplasm,"['brainstem astrocytoma', 'brain stem astrocytoma', 'astrocytoma (excluding glioblastoma) of brainstem', 'brainstem astrocytoma (excluding glioblastoma)']",4860,,,C1332608,,C7445,,,,,,
mondo:0003174,spinal cord astrocytoma,"['astrocytoma of the spinal cord', 'astrocytoma of spinal cord', 'spinal cord astrocytoma', 'spinal cord astrocytoma (excluding glioblastoma)', 'astrocytoma (excluding glioblastoma) of spinal cord', 'spinal astrocytoma']",4863,,,C0349540,,C4641,1000544,,,,,
mondo:0003175,salivary gland adenoid cystic carcinoma,"['adenoid cystic carcinoma of salivary gland', 'salivary gland adenoid cystic carcinoma', 'salivary gland adenoid cystic cancer', 'adenoid cystic carcinoma (morphologic abnormality)', 'cylindroma (morphologic abnormality)', 'adenoid cystic cancer', 'saliva-secreting gland adenoid cystic carcinoma', 'adenoid cystic carcinoma of the salivary gland']",4866,,,C0279751,,C8026,,,,,,
mondo:0003177,prostate adenoid cystic carcinoma,"['adenoid cystic carcinoma of the prostate', 'prostate adenoid cystic carcinoma', 'adenoid cystic carcinoma of prostate', 'prostate gland adenoid cystic carcinoma']",4868,,,C1335502,,C5539,,,,,,
mondo:0003180,cutaneous adenocystic carcinoma,"['adenoid cystic carcinoma of the skin', 'adenoid cystic cutaneous carcinoma', 'adenoid cystic skin carcinoma', 'skin of body adenoid cystic carcinoma', 'adenoid cystic carcinoma of skin', 'adenoid cystic eccrine carcinoma of skin', 'adenoid cystic eccrine carcinoma', 'primary cutaneous adenocystic carcinoma', 'adenoid cystic eccrine carcinoma (morphologic abnormality)']",4871,,,C0346017,,C4471,,,,,,
mondo:0003181,lung adenoid cystic carcinoma,"['adenoid cystic carcinoma of lung', 'LUACC', 'lung adenocystic carcinoma', 'adenocystic carcinoma of the lung', 'pulmonary adenocystic carcinoma', 'pulmonary adenoid cystic carcinoma', 'adenoid cystic carcinoma of the lung', 'lung adenoid cystic cancer', 'lung adenoid cystic carcinoma', 'adenocystic carcinoma of lung']",4872,,,C1334439,,C5666,,,162.9,,,
mondo:0003182,anterior horn disorder,"['disorder of ventral horn of spinal cord', 'ventral horn of spinal cord disease or disorder', 'disease of ventral horn of spinal cord', 'ventral horn of spinal cord disease']",4873,,,,,,,D016472,335.9,,,
mondo:0003184,trachea carcinoma,"['carcinoma of trachea', 'trachea carcinoma', 'trachea cancer', 'cancer of the trachea', 'carcinoma of the trachea', 'Pancoast^s tumour', 'tracheal carcinoma', 'cancer of trachea']",4876,,,C1744708,,C9347,1000599,,,,,
mondo:0003185,adenoid cystic breast carcinoma,"['adenoid cystic breast cancer', 'adenoid cystic carcinoma of breast', 'adenocystic carcinoma of breast', 'adenocystic breast carcinoma', 'adenocystic carcinoma of the breast', 'breast adenoid cystic carcinoma', 'mammary adenoid cystic carcinoma', 'adenoid cystic breast carcinoma', 'mammary adenocystic carcinoma', 'adenoid cystic carcinoma of the breast']",4877,,,C1332167,,C5130,1000071,,,,,
mondo:0003186,esophageal adenoid cystic carcinoma,"['adenoid cystic carcinoma, oesophagus', 'esophageal adenoid cystic carcinoma', 'esophagus adenoid cystic carcinoma', 'adenoid cystic oesophagus carcinoma', 'adenoid cystic carcinoma of the oesophagus', 'adenoid cystic carcinoma of oesophagus', 'adenoid cystic carcinoma of the esophagus', 'adenoid cystic esophagus carcinoma', 'oesophagus adenoid cystic carcinoma', 'adenoid cystic carcinoma, esophagus', 'adenoid cystic carcinoma of esophagus', 'esophageal adenoid cystic cancer']",4878,,,C1333441,,C5342,,,,,,
mondo:0003187,Bartholin gland adenoid cystic carcinoma,"['major vestibular gland adenoid cystic carcinoma', 'Bartholin^s gland adenoid cystic carcinoma', 'Bartholin gland adenoid cystic carcinoma']",4879,,,C1511047,,C40295,,,,,,
mondo:0003189,middle ear adenocarcinoma,"['middle Ear adenocarcinoma', 'adenocarcinoma of middle Ear', 'adenocarcinoma of the middle ear', 'adenocarcinoma of the middle Ear', 'adenocarcinoma of middle ear', 'middle ear adenocarcinoma']",4892,,,C1334758,,C6848,,,,,,
mondo:0003190,middle ear carcinoma,"['carcinoma of middle Ear', 'carcinoma of middle ear', 'middle Ear carcinoma', 'middle ear carcinoma', 'carcinoma of the middle Ear', 'carcinoma of the middle ear']",4893,,,C1334760,,C6089,,,,,,
mondo:0003191,rete ovarii adenocarcinoma,['rete ovarii adenocarcinoma'],4894,,,C3840223,,C40017,,,,,,
mondo:0003192,rete ovarii neoplasm,"['tumour of rete ovarii', 'neoplasm of rete ovarii', 'rete ovarii neoplasm (disease)', 'rete ovarii tumor', 'tumor of rete ovarii', 'rete ovarii tumour']",4895,,,C1514909,,C40016,,,,,,
mondo:0003193,bile duct adenocarcinoma,['bile duct adenocarcinoma'],4896,,,C1370800,,C27813,,,,,,
mondo:0003194,hemangioma of lung,"['pulmonary hemangioma', 'lung hemangioma']",490,,,,,,,,,,,
mondo:0003195,peritoneal serous adenocarcinoma,"['primary peritoneal serous adenocarcinoma', 'peritoneum serous adenocarcinoma']",4901,,,C1514429,,C40023,,,,,,
mondo:0003196,appendix carcinoma,"['carcinoma of the appendix', 'appendix carcinoma', 'Ca appendix', 'carcinoma of vermiform appendix', 'vermiform appendix carcinoma', 'carcinoma of appendix', 'appendix cancer']",4902,,,C0728951,,C9330,,,,,,
mondo:0003197,granular cell carcinoma,"['granular cell carcinoma', 'granular cell adenocarcinoma', 'granular cell carcinoma (morphologic abnormality)']",4903,,,C0205644,,C3681,,,,,,
mondo:0003198,small intestine adenocarcinoma,"['adenocarcinoma of small intestine', 'adenocarcinoma - small intest.', 'adenocarcinoma of small bowel', 'adenocarcinoma of the small bowel', 'adenocarcinoma of the small instestine', 'small intestinal adenocarcinoma', 'small bowel adenocarcinoma', 'adenocarcinoma of the small intestine', 'adenocarcinoma of small instestine', 'small intestine adenocarcinoma']",4906,,104075,C0278803,,C7888,1000532,,,,,
mondo:0003199,anal carcinoma,"['Ca anus', 'cancer of the anus', 'anal carcinoma', 'anal cancer', 'carcinoma of anus', 'carcinoma of the anus', 'anus carcinoma', 'cancer of anus']",4908,,,C0279637,,C9291,,,,,,
mondo:0003200,urethra adenocarcinoma,"['urethra adenocarcinoma', 'adenocarcinoma of urethra', 'adenocarcinoma of the urethra', 'urethral adenocarcinoma', 'UAD']",4910,,,C1336885,,C6167,,,,,,
mondo:0003202,pituitary gland basophilic carcinoma,"['basophil adenocarcinoma', 'basophil carcinoma (morphologic abnormality)', 'basophil carcinoma', 'basophilic carcinoma', 'pituitary gland basophil carcinoma']",4915,,,C1704778,,C27392,,,,,,
mondo:0003204,villous adenocarcinoma,"['villous adenocarcinoma (morphologic abnormality)', 'villous adenocarcinoma']",4917,,,C0334306,,C4142,,,,,,
mondo:0003205,renal pelvis adenocarcinoma,"['kidney renal pelvis adenocarcinoma', 'renal pelvis adenocarcinoma', 'kidney pelvis adenocarcinoma', 'adenocarcinoma of the renal pelvis', 'adenocarcinoma of kidney pelvis', 'adenocarcinoma of renal pelvis', 'adenocarcinoma of the kidney pelvis']",4918,,,C1335748,,C6143,,,,,,
mondo:0003206,acquired hemangioma,['acquired hemangioma'],492,,,C0856897,,C27018,,,,,,
mondo:0003208,breast secretory carcinoma,"['cystic hypersecretory breast carcinoma', 'invasive cystic hypersecretory duct breast carcinoma', 'juvenile carcinoma of breast', 'juvenile secretory carcinoma of breast', 'secretory carcinoma of the breast', 'juvenile carcinoma of the breast', 'secretory breast carcinoma', 'infiltrating cystic hypersecretory duct breast carcinoma', 'juvenile secretory breast carcinoma', 'juvenile breast carcinoma', 'cystic hypersecretory carcinoma of breast', 'secretory carcinoma of breast', 'secretory carcinoma', 'juvenile carcinoma (formerly)', 'juvenile carcinoma of the breast (morphologic abnormality)', 'juvenile secretory carcinoma of the breast', 'SBC', 'cystic hypersecretory carcinoma of the breast', 'JSCB']",4922,,,C0334371,,C4189,,C537535,,,,
mondo:0003209,thymus gland adenocarcinoma,"['thymus adenocarcinoma', 'adenocarcinoma of Thymus', 'adenocarcinoma of the Thymus', 'thymic adenocarcinoma', 'Thymus adenocarcinoma']",4923,,,C1336743,,C6459,,,,,,
mondo:0003210,intrahepatic cholangiocarcinoma,"['intrahepatic cholangiocarcinoma (bile duct cancer)', 'peripheral cholangiocarcinoma', 'intrahepatic Cholangiocellular carcinoma', 'intrahepatic carcinoma of bile duct', 'intrahepatic cholangiocarcinoma', 'intrahepatic carcinoma of the bile duct', 'intrahepatic bile duct cancer (cholangiocarcinoma)', 'cholangiocarcinoma, intrahepatic, malignant', 'ICC', 'IHCH', 'intrahepatic bile duct carcinoma']",4928,,,C0345905,,C35417,1001961,,,,,
mondo:0003211,nasal cavity adenocarcinoma,"['adenocarcinoma of the nasal cavity', 'nasal cavity adenocarcinoma', 'adenocarcinoma of nasal cavity']",4930,,,C1334920,,C6015,,,,,,
mondo:0003212,nasal cavity carcinoma,"['carcinoma of the nasal cavity', 'cancer of nasal cavity', 'nasal cavity cancer', 'cancer of the nasal cavity', 'carcinoma of nasal cavity', 'nasal cavity carcinoma']",4931,,,C1377785,,C9336,,,,,,
mondo:0003214,apocrine adenocarcinoma,"['apocrine carcinoma', 'carcinoma of apocrine gland', 'carcinoma of the apocrine gland', 'apocrine gland carcinoma', 'apocrine adenocarcinoma (morphologic abnormality)', 'apocrine gland adenocarcinoma']",4933,,,C1706827,,C4169,,,,,,
mondo:0003215,apocrine sweat gland cancer,"['cancer of apocrine sweat gland', 'malignant apocrine neoplasm', 'malignant apocrine tumor of skin', 'malignant apocrine skin tumour', 'malignant apocrine tumour', 'malignant apocrine neoplasm of the skin', 'malignant apocrine tumor of the skin', 'malignant apocrine tumour of skin', 'malignant apocrine tumour of the skin', 'malignant apocrine skin tumor', 'malignant neoplasm of apocrine sweat gland', 'malignant apocrine sweat gland neoplasm', 'malignant apocrine tumor', 'malignant apocrine skin neoplasm', 'apocrine sweat gland cancer', 'malignant apocrine neoplasm of skin']",4934,,,C1334561,,C6800,,,,,,
mondo:0003216,ureter adenocarcinoma,"['ureteral adenocarcinoma', 'adenocarcinoma of ureter', 'ureter adenocarcinoma', 'adenocarcinoma of the ureter']",4938,,,C1336873,,C6155,,,,,,
mondo:0003218,adenocarcinoma in situ,"['adenocarcinoma in situ', 'AIS']",4943,,,C0334276,,C4123,,D065311,,,,
mondo:0003219,gastroesophageal junction adenocarcinoma,"['adenocarcinoma of the cardioesophageal junction', 'adenocarcinoma of cardioesophageal junction', 'adenocarcinoma of the esophagogastric junction', 'esophagogastric adenocarcinoma', 'adenocarcinoma of gastroesophageal junction', 'adenocarcinoma - GEJ', 'gastroesophageal junction adenocarcinoma', 'adenocarcinoma of the GE junction', 'esophagogastric junction adenocarcinoma', 'adenocarcinoma of the EG junction', 'adenocarcinoma of the gastroesophageal junction']",4944,,,C1332166,,C9296,,,,,,
mondo:0003220,gallbladder carcinoma,"['cancer of gallbladder', 'gallbladder carcinoma', 'cancer of the gallbladder', 'Gall bladder carcinoma (adeno)', 'gall bladder carcinoma', 'gallbladder cancer', 'Gall bladder carcinoma (adenocarcinoma)', 'carcinoma of gall bladder', 'carcinoma of gallbladder', 'carcinoma of the gallbladder', 'carcinoma gallbladder']",4948,,,C0235782,,C3844,1001956,,,,,
mondo:0003222,central nervous system melanocytic neoplasm,"['central nervous system melanocytic tumor', 'melanocytic tumour of central nervous system', 'melanocytic tumor of the central nervous system', 'melanocytic neoplasm of the central nervous system', 'CNS melanocytic neoplasm', 'central nervous system primary melanocytic lesion', 'melanocytic tumour of the central nervous system', 'melanocytic tumour of the CNS', 'CNS melanocytic tumor', 'melanocytic tumor of CNS', 'melanocytic tumor of the CNS', 'central nervous system melanocytic tumour', 'melanocytic tumor of central nervous system', 'primary melanocytic lesions of the CNS', 'central nervous system melanocytic neoplasm', 'central nervous system melanocytic neoplasms', 'CNS melanocytic tumour', 'primary melanocytic lesion of meninges', 'melanocytic neoplasm of the CNS', 'melanocytic neoplasm of CNS', 'melanocytic tumour of CNS', 'melanocytic neoplasm of central nervous system']",4955,,,C1332887,,C5504,1000493,,,,,
mondo:0003223,meninges hemangiopericytoma,"['hemangiopericytoma of the central nervous system', 'hemangiopericytoma of meninges', 'hemangiopericytoma of the meninges', 'meningeal cluster spindle cell tumor', 'meningeal solitary fibrous tumor/hemangiopericytoma', 'meninges hemangiopericytoma', 'meningeal hemangiopericytoma', 'meningeal cluster hemangiopericytoma', 'meningeal cluster spindle cell tumour']",4957,,,C0349622,,C4660,,,,,,
mondo:0003225,bone marrow disorder,"['bone marrow disease or disorder', 'bone marrow disease', 'disease of bone marrow', 'bone marrow disorder', 'disorder of bone marrow']",4961,,,C0005956,,C34433,,D001855,289.9,,,
mondo:0003227,prosopagnosia,"['prosopagnosia (disease)', 'prosopagnosia', 'face blindness']",4970,,,,,C85031,,D020238,,,,0010528
mondo:0003231,acute nonparalytic poliomyelitis,"['non-paralytic aseptic meningitis', 'acute nonparalytic poliomyelitis', 'nonparalytic poliomyelitis']",4986,,,C0152998,,,,,045.23,A80.4,,
mondo:0003232,alcoholic pancreatitis,['alcoholic pancreatitis'],4988,,,C0376670,,,1002013,D019512,,,,
mondo:0003233,essential tremor,"['tremor, hereditary essential', 'essential hereditary tremor', 'benign essential tremor', 'shaky hand syndrome']",4990,,862,C0270736,"['0.549', '0.778', '0.0988', '-0.1375', '-0.08905', '-0.2192', '0.1218', '0.216', '-0.562', '-0.2644', '0.814', '0.3884', '0.557', '0.447', '0.3918', '0.4172', '0.382', '-0.2542', '-0.2197', '-0.868', '-0.2896', '0.0001732', '0.1957', '-0.02678', '0.1904', '0.0746', '-0.06494', '-0.6924', '0.0624', '-0.15', '-0.00405', '-0.0869', '0.3364', '-0.535', '0.1139', '-0.0297', '-0.822', '0.03778', '0.1395', '-0.4902', '0.165', '0.3767', '-0.6943', '0.3354', '1.114', '-0.5396', '-0.625', '0.11615', '0.2161', '0.2964', '-0.09216', '0.632', '-0.00533', '-0.0491', '0.3416', '-0.587', '0.4304', '0.371', '-0.1512', '-0.1329', '0.473', '0.1014', '0.4836', '-0.3809', '-0.4988', '0.7617', '-0.1663', '0.3252', '0.2263', '0.929', '-0.344', '0.387', '0.4128', '-0.374', '0.1794', '0.858', '-0.4983', '0.4956', '-0.547', '-0.3958', '-0.267', '-0.3857', '0.428', '0.0417', '0.62', '0.1271', '-0.2566', '0.1097', '0.92', '0.2406', '-0.26', '-0.701', '-0.2751', '-0.3213', '0.7603', '0.0941', '0.2832', '-0.4846', '0.1763', '-0.2961']",,0003108,D020329,333.1,G25.0,,
mondo:0003234,optic nerve astrocytoma,"['cranial nerve II astrocytoma (excluding glioblastoma)', 'astrocytoma of the optic nerve', 'astrocytoma of optic nerve', 'astrocytoma (excluding glioblastoma) of cranial nerve II', 'optic nerve astrocytoma', 'optic tract astrocytoma', 'optic tract astrocytoma (excluding glioblastoma)', 'astrocytic tumor of optic nerve', 'astrocytic tumour of optic nerve']",4991,,,C1336971,,C7533,,,,,,
mondo:0003235,optic nerve glioma,"['cranial nerve II glioma', 'optic nerve glioma', 'glioma of the optic nerve', 'glioma of optic nerve', 'glioma of cranial nerve II']",4992,,,C0346326,,C4537,,D020339,237.9,,,
mondo:0003236,atypical polypoid adenomyoma,"['atypical polypoid adenomyoma (morphologic abnormality)', 'atypical polypoid adenomyoma']",4993,,,C1300347,,C6895,,,,,,
mondo:0003237,adenomyoma of uterine corpus,"['adenomyoma of uterine corpus', 'body of uterus adenomyoma', 'adenomyoma of the uterine corpus', 'corpus uteri adenomyoma', 'adenomyoma of the uterine body', 'adenomyoma of the corpus uteri', 'adenomyoma of body of uterus', 'adenomyoma of corpus uteri', 'uterine corpus adenomyoma', 'adenomyoma of uterine body', 'adenomyoma of the body of uterus', 'uterine body adenomyoma']",4994,,,C1336903,,C6338,,,,,,
mondo:0003238,cervical adenomyoma,['cervical adenomyoma'],4995,,,C1516404,,C40231,,,,,,
mondo:0003240,thyroid gland disorder,"['thyroid gland disorders', 'thyroid gland diseases', 'thyroid disease', 'thyroid gland disorder', 'thyroid gland disease', 'disorder of thyroid gland', 'thyroid gland disease or disorder', 'disease of thyroid gland']",50,,,C0040128,,C26893,1000627,D013959,246.9,E00-E07,,
mondo:0003241,central nervous system hemangioma,"['hemangioma of the central nervous system', 'hemangioma of central nervous system', 'hemangioma of the CNS', 'hemangioma of CNS', 'central nervous system hemangioma']",501,,,C1333957,,C7004,,,,,,
mondo:0003243,hepatocellular clear cell carcinoma,"['clear cell carcinoma of the liver cells', 'clear cell hepatocellular cancer', 'clear cell hepatocellular carcinoma', 'liver cell clear cell carcinoma', 'clear cell carcinoma of liver cells', 'hepatocellular clear cell carcinoma']",5016,,,C1333067,,C5754,,,,,,
mondo:0003244,central nervous system mesenchymal non-meningothelial tumor,"['soft tissue neoplasm of the central nervous system', 'mesenchymal, non-meningothelial tumour of CNS', 'central nervous system soft tissue neoplasm', 'non-meningothelial mesenchymal tumor', 'soft tissue tumour of CNS', 'central nervous system soft tissue tumour', 'central nervous system mesenchymal, non-meningothelial neoplasm', 'mesenchymal, non-meningothelial tumour of the CNS', 'central nervous system mesenchymal, non-meningothelial tumor', 'mesenchymal, non-meningothelial tumour of central nervous system', 'soft tissue tumor of the CNS', 'CNS soft tissue tumor', 'non-meningothelial mesenchymal tumour', 'central nervous system soft tissue tumor', 'mesenchymal, non-meningothelial tumor of central nervous system', 'mesenchymal, non-meningothelial tumor of CNS', 'mesenchymal non-meningothelial tumor of the central nervous system', 'soft tissue tumour of the CNS', 'CNS soft tissue neoplasm', 'soft tissue neoplasm of CNS', 'soft tissue tumour of the central nervous system', 'central nervous system mesenchymal, non-meningothelial tumour', 'mesenchymal non-meningothelial tumour of the central nervous system', 'soft tissue neoplasm of central nervous system', 'soft tissue tumour of central nervous system', 'soft tissue tumor of the central nervous system', 'soft tissue neoplasm of the CNS', 'CNS soft tissue tumour', 'mesenchymal, non-meningothelial tumor of the CNS', 'soft tissue tumor of central nervous system', 'soft tissue tumor of CNS']",502,,,C1332893,,C5449,,,,,,
mondo:0003245,aflatoxin-related hepatocellular carcinoma,"['aflatoxins-related hepatocellular cancer', 'aflatoxins-related hepatocellular carcinoma']",5022,,,C1332222,,C27922,,,,,,
mondo:0003246,sclerosing hepatic carcinoma,"['sclerosing hepatic carcinoma', 'scirrhous hepatocellular carcinoma', 'sclerosing hepatocellular carcinoma', 'scirrhous hepatocellular cancer']",5026,,,C1266018,,C27388,,,,,,
mondo:0003248,adult pineal parenchymal tumor,"['adult pineal parenchymal cell tumour', 'parenchymal tumor of adult pineal gland', 'pineal parenchymal cell tumour', 'adult pineal parenchymal cell tumor', 'adult pineal gland tumour', 'parenchymal tumor of the adult pineal gland', 'adult pineal parenchymal tumor', 'parenchymal tumour of adult pineal gland', 'parenchymal tumour of the adult pineal gland', 'pineal parenchymal cell neoplasm of adults', 'pineal parenchymal cell tumor', 'adult pineal gland neoplasm', 'adult pineal parenchymal cell neoplasm', 'adult pineal parenchymal neoplasm', 'parenchymal neoplasm of the adult pineal gland', 'parenchymal neoplasm of adult pineal gland', 'adult pineal gland tumor']",5031,,,C0280794,,C8273,,,,,,
mondo:0003249,pineal gland cancer,"['tumour of the pineal region', 'malignant neoplasm of the pineal gland', 'pineocytic tumour', 'malignant pineal gland tumor', 'tumor of the pineal region', 'pineal body cancer', 'malignant pineal region neoplasm', 'malignant pineal area neoplasm', 'cancer of pineal body', 'malignant pineal gland tumour', 'malignant tumour of pineal gland', 'malignant pineal body neoplasm', 'malignant pineal gland neoplasm', 'malignant neoplasm of pineal body', 'pinealoma', 'neoplasm of the pineal region', 'malignant neoplasm of pineal gland', 'malignant pineal area tumor', 'malignant pineal region tumour', 'malignant tumor of the pineal gland', 'malignant tumor of pineal gland', 'pineocytic tumor', 'malignant pineal region tumor', 'malignant tumour of the pineal gland', 'malignant pineal area tumour']",5032,,,C0031941,,C6965,,,194.4,,,
mondo:0003250,benign granular cell tumor,"['benign granular cell tumor', 'benign granular cell neoplasm', 'myoblastoma', 'granular cell tumor, benign', 'benign granular cell myoblastoma']",5039,,,C0027043,,C3252,,D009379,,,,
mondo:0003251,esophageal granular cell tumor,"['granular cell tumour of oesophagus', 'granular cell neoplasm of oesophagus', 'malignant granular cell esophageal tumor', 'granular cell esophagus neoplasm', 'esophageal granular cell neoplasm', 'granular cell oesophagus myoblastoma', 'granular cell tumour of the oesophagus', 'granular cell tumor of esophagus', 'esophageal granular cell tumor', 'granular cell neoplasm of esophagus', 'oesophagus granular cell tumour', 'granular cell neoplasm of the oesophagus', 'esophageal granular cell myoblastoma', 'granular cell esophagus tumor', 'granular cell myoblastoma of esophagus', 'malignant granular cell esophageal tumour', 'granular cell esophagus myoblastoma', 'granular cell myoblastoma of the oesophagus', 'granular cell myoblastoma of oesophagus', 'granular cell neoplasm of the esophagus', 'granular cell esophageal tumor', 'granular cell tumor of the esophagus', 'granular cell myoblastoma of the esophagus', 'granular cell oesophagus neoplasm', 'granular cell esophageal tumour', 'granular cell oesophagus tumour', 'esophagus granular cell tumor']",5040,,,C1333448,,C5700,,,,,,
mondo:0003252,granular cell cancer,"['granular cell tumor, malignant (morphologic abnormality)', 'malignant granular cell myoblastoma', 'malignant granular cell tumor', 'myoblastoma, malignant', 'malignant granular cell neoplasm', 'granular cell tumor, malignant', 'malignant granular cell tumour']",5042,,,C0334618,,C4336,,,171.9,,,
mondo:0003253,vulvar granular cell tumor,"['vulvar granular cell tumor', 'mammalian vulva granular cell tumor', 'granular cell tumor of mammalian vulva', 'granular cell tumour of mammalian vulva', 'mammalian vulva granular cell tumour']",5043,,,C1520083,,C40328,,,,,,
mondo:0003254,cardiac granular cell neoplasm,"['granular cell neoplasm of heart', 'heart granular cell tumor', 'heart granular cell tumour', 'granular cell tumor of heart', 'granular cell neoplasm of the heart', 'Cardiac granular cell tumour', 'Cardiac granular cell neoplasm', 'granular cell tumour of heart', 'granular cell tumor of the heart', 'granular cell tumour of the heart', 'Cardiac granular cell tumor']",5044,,,C1332845,,C5360,,,,,,
mondo:0003255,mediastinal granular cell myoblastoma,"['mediastinal granular cell tumor', 'mediastinal granular cell neoplasm', 'mediastinal granular cell myoblastoma', 'mediastinum granular cell tumor', 'granular cell neoplasm of mediastinum', 'granular cell tumor of the mediastinum', 'granular cell myoblastoma of the mediastinum', 'mediastinal granular cell tumour', 'granular cell tumor of mediastinum', 'mediastinum granular cell tumour', 'granular cell tumour of mediastinum', 'granular cell neoplasm of the mediastinum', 'granular cell tumour of the mediastinum', 'granular cell myoblastoma of mediastinum']",5046,,,C1334656,,C6601,,,,,,
mondo:0003256,neurohypophysis granular cell tumor,"['granular cell tumour of the neurohypophysis', 'neurohypophysis granular cell tumor', 'granular cell tumour of the posterior pituitary gland', 'granular cell tumour of Neurohypophysis', 'granular cell tumor of Neurohypophysis', 'granular cell tumor of the Neurohypophysis (WHO grade I)', 'granular cell tumour of the Neurohypophysis (WHO grade I)', 'granular cell tumour of neurohypophysis', 'granular cell tumor of the neurohypophysis', 'granular cell tumor of the posterior pituitary gland']",5047,,,C1333873,,C7017,1000285,,,,,
mondo:0003257,posterior pituitary gland neoplasm,"['posterior pituitary tumor', 'posterior pituitary tumour', 'posterior pituitary gland tumour', 'posterior pituitary gland neoplasm', 'Neurohypophysis tumor', 'PITUICYTOMA, benign', 'tumor of neurohypophysis', 'neoplasm of neurohypophysis', 'neurohypophysis tumour', 'neurohypophysis tumor', 'posterior pituitary gland tumor', 'Neurohypophysis neoplasm', 'neurohypophysis neoplasm (disease)', 'Neurohypophysis tumour', 'tumour of neurohypophysis', 'posterior pituitary neoplasm']",5048,,,C1334957,,C7157,,,,,,
mondo:0003258,hobnail hemangioma,"['hobnail hemangioma', 'Targetoid Hemosiderotic hemangioma']",505,,,C0346076,,C27506,,,,,,
mondo:0003260,adult cerebellar neoplasm,"['adult cerebellar tumours', 'adult cerebellar tumor', 'cerebellar neoplasm of adults', 'tumour of adult cerebellum', 'adult cerebellar tumors', 'tumor of adult cerebellum', 'adult cerebellar neoplasms', 'tumor of the adult cerebellum', 'adult cerebellar neoplasm', 'neoplasm of the adult cerebellum', 'tumour of the adult cerebellum', 'adult cerebellar tumour', 'neoplasm of adult cerebellum']",5056,,,C1332197,,C5968,,,,,,
mondo:0003261,papillary meningioma of the cerebellum,"['cerebellar papillary meningioma', 'cerebellum papillary meningioma', 'papillary meningioma of cerebellum', 'papillary meningioma of the cerebellum']",5057,,,C1332902,,C5270,,,,,,
mondo:0003262,rhabdoid meningioma,"['papillary meningioma (morphologic abnormality)', 'papillary meningioma', 'meningioma, rhabdoid (morphologic abnormality)', 'rhabdoid meningioma', 'meningioma, rhabdoid']",5058,,,C0259786,,C6909,,,,,,
mondo:0003263,childhood cerebellar neoplasm,"['childhood neoplasm of cerebellum', 'pediatric neoplasm of cerebellum', 'childhood tumour of cerebellum', 'paediatric cerebellar tumour', 'pediatric tumor of cerebellum', 'childhood cerebellar neoplasm', 'paediatric neoplasm of the cerebellum', 'childhood cerebellar neoplasms', 'pediatric neoplasm of the cerebellum', 'childhood tumour of the cerebellum', 'paediatric tumour of the cerebellum', 'childhood tumor of the cerebellum', 'paediatric tumour of cerebellum', 'childhood cerebellar tumor', 'childhood tumor of cerebellum', 'paediatric neoplasm of cerebellum', 'childhood cerebellar tumour', 'childhood cerebellar tumors', 'pediatric tumor of the cerebellum', 'paediatric cerebellar neoplasm', 'childhood cerebellar tumours', 'pediatric cerebellar tumor', 'pediatric cerebellar neoplasm', 'childhood neoplasm of the cerebellum']",5059,,,C1332959,,C5970,,,,,,
mondo:0003264,basosquamous carcinoma,"['basosquamous tumor, malignant', 'skin mixed basal and squamous cell carcinoma', 'skin basosquamous cell carcinoma', 'metatypical carcinoma', 'Basisquamous cell carcinoma', 'metatypical carcinoma (morphologic abnormality)', 'basosquamous cell carcinoma', 'basosquamous carcinoma']",5063,,,C0007118,,C2922,1000529,D002281,,,,
mondo:0003265,adjustment disorder,"['disorders, adjustment', 'adjustment disorder', 'adjustment reaction', 'disorder, adjustment', 'disorders, reactive', 'disorder, reactive', 'adjustment disease']",507,,,,,C92191,,D000275,309.9,,,
mondo:0003266,ependymal tumor,"['ependymal neoplasm', 'ependymal tumor', 'ependymomal tumor', 'ependymomal tumour', 'ependymal tumours', 'ependymal tumors']",,,301,CN203416,,C6770,1000027,,,,,
mondo:0003268,mixed glioma,"['mixed glioma (morphologic abnormality)', 'mixed neuroglial neoplasm', 'mixed glial neoplasm', 'mixed gliomas', 'mixed neuroglial tumour', 'glioma, mixed, malignant', 'mixed glial tumor', 'mixed glioma', 'mixed neuroglial tumor', 'mixed glial tumour', 'glioma, mixed']",5076,,,C0259783,,C3903,,,,,,
mondo:0003271,iodine hypothyroidism,,5083,,,C0154159,,,,,244.2,,,
mondo:0003272,mixed epithelial stromal tumor,['mixed epithelial stromal tumor'],5088,,,C1334602,,C37265,,,,,,
mondo:0003273,sternum cancer,"['malignant tumour of the sternum', 'malignant tumor of the sternum', 'sternum cancer', 'sternal tumour', 'malignant sternal tumour', 'malignant tumor of sternum', 'malignant sternal neoplasm', 'malignant neoplasm of sternum', 'neoplasm of sternum', 'malignant sternal tumor', 'malignant sternum neoplasm', 'malignant neoplasm of the sternum', 'malignant tumour of sternum', 'cancer of sternum']",5090,,,C1382025,,C8408,,,,,,
mondo:0003274,thoracic cancer,"['thorax cancer', 'malignant tumour of thorax', 'malignant tumor of thorax', 'malignant thoracic neoplasm', 'thorax neoplasm', 'malignant neoplasm of the thorax', 'malignant thoracic tumour', 'thoracic tumor', 'tumor of thorax', 'malignant neoplasm of thoracic segment of trunk', 'malignant neoplasm of thorax', 'malignant tumour of the thorax', 'cancer of thoracic segment of trunk', 'tumour of thorax', 'malignant thoracic tumor', 'malignant thoracic segment of trunk neoplasm', 'malignant tumor of the thorax', 'thoracic tumour', 'thoracic segment of trunk cancer']",5093,,,C0153661,,C3576,,,195.1,,,
mondo:0003275,middle ear cancer,"['malignant neoplasm of middle ear', 'malignant middle ear neoplasm', 'malignant tumour of middle Ear', 'malignant tumor of middle Ear', 'middle ear cancer', 'malignant middle Ear tumour', 'malignant tumour of the middle Ear', 'tumor of the middle ear', 'tumour of the middle ear', 'malignant middle Ear tumor', 'cancer of middle ear', 'malignant neoplasm of the middle Ear', 'malignant tumor of the middle Ear']",5099,,,,,C4765,,,,,,
mondo:0003276,middle ear disorder,"['disorder of middle ear', 'middle Ear disorder', 'middle ear disease', 'middle ear disease or disorder', 'disease of middle ear']",5100,,,C0271428,,C27065,,,,H65-H75,,
mondo:0003277,malignant ear neoplasm,"['malignant neoplasm of the Ear', 'malignant tumor of ear', 'auricular cancer', 'malignant neoplasm of Ear', 'malignant ear neoplasm', 'malignant tumor of Ear', 'malignant Ear tumor', 'malignant tumour of ear', 'malignant Ear neoplasm', 'malignant tumor of the Ear', 'malignant Ear tumour', 'ear cancer', 'cancer of ear', 'malignant tumour of the Ear', 'malignant neoplasm of ear', 'malignant tumour of Ear']",5101,,,C0751094,,C9337,,D004428,,,,
mondo:0003278,inner ear cancer,"['malignant neoplasm of internal ear', 'malignant internal ear neoplasm', 'cancer of internal ear', 'internal ear cancer']",5102,,,C1512779,,C39784,,,,,,
mondo:0003279,testicular infarct,"['testicular infarction', 'infarction of testis']",5104,,,C0392041,,C27617,,,,,,
mondo:0003280,swayback,['swayback of sheep'],5112,,,,,,,D013540,,,,
mondo:0003281,ovarian cystic teratoma,['ovary cystic teratoma'],5118,,,C1335155,,C7283,,,,,,
mondo:0003282,ovarian cyst,"['cysts, corpus luteum', 'cyst, ovarian', 'ovarian cyst (disease)', 'cysts, ovarian', 'ovarian cyst', 'cyst, corpus luteum', 'corpus luteum cyst', 'corpus luteum cysts']",5119,,,,,,,D010048,620.2,,,0000138
mondo:0003283,epididymal neoplasm,"['neoplasm of epididymis', 'epididymis neoplasm (disease)', 'tumour of epididymis', 'epididymal neoplasm', 'epididymis tumour', 'tumor of epididymis', 'epididymis tumor']",512,,,C0346239,,C39958,,,239.5,,,
mondo:0003284,mediastinum leiomyoma,"['leiomyoma of the mediastinum', 'mediastinal leiomyoma', 'mediastinum leiomyoma', 'leiomyoma of mediastinum']",5123,,,C1334659,,C6598,,,,,,
mondo:0003285,fallopian tube leiomyoma,"['leiomyoma of fallopian tube', 'fallopian tube leiomyoma']",5124,,,C1517115,,C40127,,,,,,
mondo:0003286,extrahepatic bile duct leiomyoma,"['leiomyoma of extrahepatic bile duct', 'extrahepatic bile duct leiomyoma', 'leiomyoma of the extrahepatic bile duct']",5125,,,C1333507,,C5855,,,,,,
mondo:0003287,central nervous system leiomyoma,"['leiomyoma of CNS', 'leiomyoma of the CNS', 'leiomyoma of the central nervous system', 'leiomyoma of central nervous system', 'central nervous system leiomyoma']",5126,,,C1334382,,C6998,,,,,,
mondo:0003288,bizarre leiomyoma,"['bizarre leiomyoma', 'atypical leiomyoma', 'pleomorphic leiomyoma', 'Symplastic leiomyoma']",5127,,,C0334478,,C4257,,,,,,
mondo:0003289,deep leiomyoma,['deep leiomyoma'],5128,,,C1333266,,C6512,,,,,,
mondo:0003290,simple partial epilepsy,,5129,,,,,,,,345.51,,,
mondo:0003291,leiomyoma cutis,"['zone of skin leiomyoma', 'cutaneous leiomyoma', 'cutaneous (skin) leiomyoma', 'leiomyoma cutis', 'skin leiomyoma', 'leiomyoma of skin', 'leiomyoma of the skin', 'leiomyoma of zone of skin']",5132,,,C0346064,,C4482,,,,,,
mondo:0003292,anus leiomyoma,"['leiomyoma of the anus', 'leiomyoma of anus', 'anal leiomyoma', 'anus leiomyoma']",5134,,,C1332266,,C5608,,,,,,
mondo:0003293,lung leiomyoma,"['leiomyoma of the lung', 'pulmonary leiomyoma', 'leiomyoma of lung', 'lung leiomyoma']",5136,,,C1334447,,C5660,,,,,,
mondo:0003294,pericardium leiomyoma,"['leiomyoma of pericardium', 'pericardial leiomyoma', 'leiomyoma of the pericardium', 'pericardium leiomyoma']",5137,,,C1335380,,C6743,,,,,,
mondo:0003295,leiomyomatosis,"['leiomyomatosis, no ICD-O subtype (morphologic abnormality)', 'leiomyomatosis', 'leiomyomatosis, no ICD-O subtype']",5138,,,C0206654,,C3748,,D018231,,,,
mondo:0003296,cellular leiomyoma,"['cellular leiomyoma (morphologic abnormality)', 'cellular leiomyoma']",5139,,,C0334477,,C4256,,,,,,
mondo:0003297,gallbladder leiomyoma,"['gall bladder leiomyoma', 'leiomyoma of gallbladder', 'leiomyoma of the gallbladder', 'gallbladder leiomyoma', 'leiomyoma of gall bladder']",5140,,,C1333745,,C5747,,,,,,
mondo:0003298,vulvar leiomyoma,"['leiomyoma of mammalian vulva', 'vulvar leiomyoma', 'mammalian vulva leiomyoma']",5142,,,C1520087,,C40326,,,,,,
mondo:0003299,colorectal leiomyoma,"['leiomyoma of the large bowel', 'leiomyoma of large intestine', 'leiomyoma of the large intestine', 'leiomyoma of large bowel', 'large bowel leiomyoma', 'colorectal leiomyoma', 'colorectum leiomyoma', 'large intestine leiomyoma']",5143,,,C1333113,,C5677,,,,,,
mondo:0003300,appendix leiomyoma,"['leiomyoma of the appendix', 'leiomyoma of appendix', 'appendiceal leiomyoma', 'leiomyoma of vermiform appendix', 'vermiform appendix leiomyoma', 'appendix leiomyoma']",5146,,,C1332327,,C5514,,,,,,
mondo:0003301,dartoic leiomyoma,"['dartoic leiomyoma', 'dartos muscle leiomyoma', 'leiomyoma of dartos muscle', 'dartoic myoma']",5147,,,C0346066,,C4483,,,215.9,,,
mondo:0003302,epithelioid neurofibroma,['epithelioid neurofibroma'],5149,,,C1275264,,C6558,,,215.9,,,
mondo:0003303,neurofibroma of gallbladder,"['gallbladder neurofibroma', 'neurofibroma of gallbladder', 'neurofibroma of the gallbladder', 'gall bladder neurofibroma', 'neurofibroma of gall bladder']",5150,,,C1333751,,C5746,,,,,,
mondo:0003304,plexiform neurofibroma,"['plexiform neurofibroma', 'plexiform neurofibroma (disease)']",5151,,,C0206728,,C3797,0000658,D018318,215.9,,,0009732
mondo:0003305,cellular neurofibroma,['cellular neurofibroma'],5152,,,C1516371,,C41427,,,,,,
mondo:0003306,atypical neurofibroma,['atypical neurofibroma'],5153,,,C1510961,,C41426,,,,,,
mondo:0003307,multiple mucosal neuroma,['multiple mucosal neuromas'],5155,,,C1334828,,C6559,,,,,,
mondo:0003308,pleural mesothelioma,"['pleural mesothelioma (disease)', 'mesothelioma of the pleura', 'benign pleural mesothelioma', 'pleural mesothelioma (disease), benign', 'pleura mesothelioma', 'mesothelioma of pleura', 'pleural mesothelioma']",5157,,,,,C9351,1000485,,,,,0100002
mondo:0003310,Monckeberg arteriosclerosis,['Mönckeberg arteriosclerosis'],5161,,,C0887866,,C35770,,,,,,
mondo:0003311,endometrial stromal tumor,"['endometrial stromal neoplasm', 'endometrial stroma tumour', 'tumour of endometrial stroma', 'endometrial stroma tumor', 'neoplasm of endometrial stroma', 'tumor of endometrial stroma', 'endometrial stromal tumour (morphologic abnormality)', 'endometrial stromal tumor (morphologic abnormality)']",5166,,,C0334695,,,1000920,D036821,239.5,,,
mondo:0003312,ovarian endometrioid stromal and related neoplasms,"['endometrioid stromal and related neoplasms of ovary', 'ovarian endometrioid stromal sarcoma', 'ovarian endometrioid stromal and related neoplasms', 'ovary endometrioid stromal and related neoplasms']",5169,,,C4288544,,C40065,,,,,,
mondo:0003313,endometrioid stromal sarcoma of the vagina,"['vaginal endometrial stromal sarcoma', 'vagina endometrioid stromal sarcoma', 'endometrioid stromal sarcoma of vagina', 'endometrioid stromal sarcoma of the vagina']",5170,,,C3642329,,C40270,,,,,,
mondo:0003314,endometrioid stromal and related neoplasms of the vagina,"['vaginal endometrial stromal tumour', 'vagina endometrioid stromal and related neoplasms', 'vaginal endometrial stromal tumor', 'endometrioid stromal and related neoplasms of vagina', 'endometrioid stromal and related neoplasms of the vagina', 'endometrioid stromal and related tumors of the vagina', 'endometrioid stromal and related tumours of the vagina']",5171,,,C4289585,,C40269,,,,,,
mondo:0003315,endometrium carcinoma in situ,"['stage 0 endometrium carcinoma', 'endometrium in situ carcinoma', 'carcinoma in situ of endometrium', 'endometrial carcinoma in situ']",5172,,,C0346191,,,,,233.2,D07.0,,
mondo:0003316,nonanaplastic kidney Wilms tumor,"['nonanaplastic renal Wilms tumour', 'nonanaplastic renal Wilm^s tumour', 'nonanaplastic renal Wilms^ tumor', 'nonanaplastic kidney Wilms tumor', 'nonanaplastic renal Wilm^s tumor', 'nonanaplastic renal Wilms tumor', 'nonanaplastic renal Wilms^ tumour']",,,,C1335062,,C6951,,,,,,
mondo:0003317,metachronous kidney Wilms^ tumor,"['metachronous Wilms tumour of the kidney', 'metachronous Wilms tumor', 'metachronous Wilms tumor of the kidney', 'metachronous Wilms tumour', 'metachronous Wilms^ tumor', 'metachronous Wilms^ tumour']",5178,,,C1334705,,C38158,,,,,,
mondo:0003318,mixed cell type kidney Wilms^ tumor,"['mixed cell type nephroblastoma', 'mixed cell type renal Wilms^ tumour', 'Mixed cell type Wilms tumour', 'mixed cell type renal adenosarcoma', 'Mixed cell type Wilms tumor', 'mixed cell type renal Wilm^s tumour', 'mixed cell type renal Wilms^ tumor', 'mixed cell type renal Wilms tumour', 'mixed cell type kidney Wilms tumour', 'mixed cell type renal Wilm^s tumor', 'mixed cell type kidney adenosarcoma', 'mixed cell type kidney Wilms tumor', 'mixed cell type renal Wilms tumor']",5179,,,C0279611,,C9149,,,,,,
mondo:0003319,scrotum neoplasm,"['malignant tumour of scrotum', 'scrotal tumour', 'tumor of the scrotum', 'neoplasm of the scrotum', 'tumour of the scrotum', 'tumour of scrotum', 'scrotal tumor', 'tumor of scrotum', 'malignant tumor of scrotum', 'scrotum neoplasm (disease)', 'scrotum tumor', 'scrotum tumour', 'neoplasm of scrotum', 'scrotal Ca', 'malignant scrotal neoplasm', 'scrotal neoplasm']",518,,,C0341790,,C4380,,,239.5,,,
mondo:0003320,blastema predominant kidney Wilms tumor,"['blastema predominant renal adenosarcoma', 'blastema predominant renal Wilms tumour', 'blastema predominant renal Wilm^s tumour', 'blastema predominant Wilms tumor', 'blastema predominant kidney Wilms tumor', 'blastema predominant renal Wilm^s tumor', 'blastema predominant kidney Wilms^ tumour', 'blastema predominant nephroblastoma', 'blastema predominant Wilms tumour', 'blastema predominant kidney adenosarcoma', 'blastema predominant kidney Wilms^ tumor', 'blastema predominant renal Wilms tumor', 'blastema predominant renal Wilms^ tumour', 'blastema predominant renal Wilms^ tumor']",5182,,,C0279609,,C9147,,,,,,
mondo:0003321,hereditary Wilms tumor,"['familial Wilms tumour', 'hereditary Wilms tumor', 'hereditary Wilms^ tumour', 'familial Wilms^ tumor', 'hereditary nephroblastoma', 'WT1', 'familial Wilms^ tumour', 'hereditary renal adenosarcoma', 'hereditary kidney adenosarcoma', 'hereditary Wilms^ tumor', 'familial Wilms tumor']",5183,,,C0677779,,C8496,,,,,,
mondo:0003322,epithelial predominant Wilms^ tumor,"['epithelial predominant renal Wilms tumor', 'epithelial predominant kidney adenosarcoma', 'epithelial predominant Wilms tumor', 'epithelial predominant nephroblastoma', 'epithelial predominant Wilms tumour', 'epithelial predominant renal Wilm^s tumour', 'epithelial predominant renal Wilms^ tumor', 'epithelial predominant renal Wilm^s tumor', 'epithelial predominant kidney Wilms tumor', 'epithelial predominant renal Wilms^ tumour', 'epithelial predominant renal adenosarcoma', 'epithelial predominant kidney Wilms tumour', 'epithelial predominant renal Wilms tumour']",5189,,,C0279608,,C9146,,,,,,
mondo:0003325,nodular ganglioneuroblastoma,"['ganglioneuroblastoma, nodular']",5193,,,C1517445,,C42058,,,,,,
mondo:0003326,intermixed schwannian stroma-rich ganglioneuroblastoma,"['ganglioneuroblastoma, intermixed', 'ganglioneuroblastoma, intermixed (Schwannian Stroma-rich)']",5194,,,C1517444,,C42057,,,,,,
mondo:0003327,peripheral ganglioneuroblastoma,"['peripheral ganglioneuroblastoma', 'PNS ganglioneuroblastoma', 'peripheral nervous system ganglioneuroblastoma', 'peripheral nervous system ganglioneuroblastoma (disease)']",5195,,,C1335387,,C6594,,,,,,
mondo:0003328,fallopian tube adenomatoid tumor,['fallopian tube adenomatoid tumor'],5196,,,C1517110,,C40129,,,,,,
mondo:0003329,ureteral obstruction,"['ureteral obstruction', 'ureteral obstruction (disease)']",5199,,,,,,,D014517,593.4,,,0006000
mondo:0003330,urinary tract obstruction,"['urinary obstruction', 'obstructive uropathy']",5200,,,C0178879,,C3675,,,599.60,,,
mondo:0003331,ovarian monodermal teratoma,"['monodermal teratoma (morphologic abnormality)', 'ovarian monodermal teratoma', 'monodermal teratoma']",5207,,,C1302569,,C7286,,,,,,
mondo:0003332,malignant struma ovarii,"['struma ovarii, malignant', 'struma ovarii, malignant (morphologic abnormality)']",5208,,,C0334525,,C4291,,,,,,
mondo:0003333,benign struma ovarii,"['struma ovarii, benign', 'benign struma ovarii']",5209,,,C1511104,,C40012,,,,,,
mondo:0003334,demyelinating polyneuropathy,['peripheral demyelinating neuropathy'],5214,,,C0270922,,C27062,,,356.9,,,
mondo:0003335,chronic polyneuropathy,"['polyneuropathy, chronic']",5221,,,C1167650,,C36071,,,,,,
mondo:0003336,acute necrotizing encephalitis,"['acute necrotizing encephalitis', 'ANE', 'acute necrotizing encephalopathy']",5222,,,C0338418,,C35383,,D004684,049.8,,,
mondo:0003337,acute hemorrhagic encephalitis,['acute hemorrhagic encephalitis'],5224,,,C1332149,,C35796,,,,,,
mondo:0003340,malignant glomus tumor,"['malignant glomus tumor', 'malignant glomus neoplasm', 'glomus tumor, malignant', 'glomangiosarcoma']",5233,,,C1266111,,C4221,,,,,,
mondo:0003341,subungual glomus tumor,['subungual glomus tumor'],5236,,,C1304510,,C36079,,,228.09,,,
mondo:0003342,benign perivascular tumor,"['benign Pericytic tumor', 'benign perivascular tumor', 'pericytic neoplasm, benign', 'benign perivascular neoplasm', 'benign Pericytic tumour', 'benign Pericytic neoplasm']",5238,,,C1332532,,C6529,,,,,,
mondo:0003343,retinal hemangioblastoma,"['vasculature of retina hemangioblastoma', 'retinal hemangioblastoma', 'retinal capillary hemangioblastoma', 'hemangioblastoma of vasculature of retina']",5240,,,C1514915,,C39783,,,,,,
mondo:0003345,hilar cholangiocarcinoma,"['perihilar extrahepatic bile duct carcinoma', 'hilar cholangiocarcinoma', 'hilar portion of hepatic duct cholangiocarcinoma', 'Klatskin tumour', 'cholangiocarcinoma of hilar portion of hepatic duct', 'perihilar cholangiocarcinoma', 'Klatskin^s tumor', 'hilar CCA', 'Klatskin^s tumour', 'hilar cholangiocellular carcinoma', 'hilar CC', 'Klatskin tumor']",5246,,99978,C0206702,,C36077,1001005,D018285,,,,
mondo:0003346,central nervous system vasculitis,"['central nervous system vasculitis', 'vasculitis of central nervous system']",525,,,C0751878,,C84622,,D020293,,,,
mondo:0003347,inflammatory leiomyosarcoma,['inflammatory leiomyosarcoma'],5251,,,C1334179,,C27495,,,,,,
mondo:0003348,conventional leiomyosarcoma,"['classic leiomyosarcoma', 'conventional leiomyosarcoma']",5253,,,C1333157,,C9428,,,,,,
mondo:0003349,central nervous system leiomyosarcoma,"['leiomyosarcoma of the central nervous system', 'leiomyosarcoma of central nervous system', 'central nervous system leiomyosarcoma', 'leiomyosarcoma of CNS', 'leiomyosarcoma of the CNS', 'CNS leiomyosarcoma']",5254,,,C1334385,,C6999,,,,,,
mondo:0003350,granular cell leiomyosarcoma,['granular cell leiomyosarcoma'],5258,,,C1333871,,C27494,,,,,,
mondo:0003351,colon leiomyosarcoma,"['colon leiomyosarcoma', 'leiomyosarcoma of the colon', 'leiomyosarcoma of colon', 'colonic leiomyosarcoma']",5259,,,C1333093,,C5494,,,,,,
mondo:0003352,colon sarcoma,"['sarcoma of colon', 'colon sarcoma', 'colonic sarcoma', 'sarcoma of the colon']",5260,,,C1333098,,C5495,,,,,,
mondo:0003353,heart leiomyosarcoma,"['leiomyosarcoma of heart', 'Cardiac leiomyosarcoma', 'leiomyosarcoma of the heart', 'heart leiomyosarcoma']",5261,,,C1332848,,C5364,,,,,,
mondo:0003354,heart sarcoma,"['sarcoma of the heart', 'Cardiac sarcoma', 'heart sarcoma', 'sarcoma of heart', 'cardiac sarcoma']",5262,,,C0238152,,C7723,,,,,,
mondo:0003355,ovary leiomyosarcoma,"['ovary leiomyosarcoma', 'leiomyosarcoma of the ovary', 'ovarian leiomyosarcoma', 'leiomyosarcoma of ovary']",5263,,,C1335163,,C5234,0006718,,,,,
mondo:0003356,epithelioid leiomyosarcoma,['epithelioid leiomyosarcoma'],5264,,,C0205815,,C3700,,,,,,
mondo:0003357,lung leiomyosarcoma,"['leiomyosarcoma of the lung', 'lung leiomyosarcoma', 'pulmonary leiomyosarcoma', 'leiomyosarcoma of lung']",5265,,,C1334448,,C5667,,,,,,
mondo:0003358,anus leiomyosarcoma,"['leiomyosarcoma of the anus', 'leiomyosarcoma of anus', 'anus leiomyosarcoma', 'anal leiomyosarcoma']",5267,,,C1332267,,C5599,,,,,,
mondo:0003359,myxoid leiomyosarcoma,"['myxoid leiomyosarcoma', 'myxoid leiomyosarcoma (morphologic abnormality)']",5268,,,C0205816,,C3701,,,,,,
mondo:0003360,small intestine leiomyosarcoma,"['smooth muscle connective tissue tumour', 'leiomyosarcoma of small intestine', 'leiomyosarcoma of the small bowel', 'leiomyosarcoma of the small intestine', 'smooth muscle connective tissue tumor', 'leiomyosarcoma of small bowel', 'small bowel leiomyosarcoma', 'small intestine leiomyosarcoma', 'small intestinal leiomyosarcoma']",5271,,104076,C0920305,,C7085,,,,,,
mondo:0003361,small intestinal sarcoma,"['sarcoma, small intestinal', 'small intestine sarcoma', 'sarcoma of small intestine', 'sarcoma of the small intestine', 'small intestinal sarcoma', 'sarcoma of small bowel', 'small bowel sarcoma', 'sarcoma of the small bowel']",5272,,,C1336007,,C5335,,,,,,
mondo:0003362,cutaneous leiomyosarcoma,"['cutaneous leiomyosarcoma (disease)', 'leiomyosarcoma of skin', 'zone of skin leiomyosarcoma', 'leiomyosarcoma of zone of skin', 'cutaneous leiomyosarcoma', 'leiomyosarcoma of the skin', 'skin leiomyosarcoma']",5273,,,C0346067,,C4484,,,,,,0006755
mondo:0003363,malignant dermis tumor,"['malignant dermal neoplasm', 'cancer of dermis', 'malignant tumor of dermis', 'malignant tumor of the dermis', 'malignant tumour of the dermis', 'malignant neoplasm of dermis', 'dermis cancer', 'malignant dermis tumor', 'malignant neoplasm of the dermis', 'malignant dermis neoplasm', 'malignant tumour of dermis']",5274,,,C0346811,,C4574,,,,,,
mondo:0003364,gallbladder leiomyosarcoma,"['leiomyosarcoma of gallbladder', 'gall bladder leiomyosarcoma', 'gallbladder leiomyosarcoma', 'leiomyosarcoma of gall bladder', 'leiomyosarcoma of the gallbladder']",5275,,,C1333746,,C5841,,,,,,
mondo:0003365,esophagus leiomyosarcoma,"['esophageal leiomyosarcoma', 'leiomyosarcoma of esophagus', 'leiomyosarcoma of the esophagus', 'esophagus leiomyosarcoma', 'leiomyosarcoma of oesophagus', 'leiomyosarcoma of the oesophagus']",5276,,,C1333454,,C5334,,,,,,
mondo:0003366,hydrarthrosis,,528,,,,,,,D006833,719.08,,,
mondo:0003367,gastric leiomyosarcoma,"['gastric leiomyosarcoma', 'stomach leiomyosarcoma', 'leiomyosarcoma of stomach', 'gastric leiomyosarcoma (disease)']",5280,,,C0744295,,C27200,,,,,,0031025
mondo:0003368,prostate leiomyosarcoma,"['leiomyosarcoma of the prostate', 'leiomyosarcoma of prostate', 'prostate gland leiomyosarcoma', 'leiomyosarcoma of prostate gland', 'prostate leiomyosarcoma']",5282,,,C1335511,,C5526,,,,,,
mondo:0003369,vagina leiomyosarcoma,"['vagina leiomyosarcoma', 'leiomyosarcoma of vagina', 'vaginal leiomyosarcoma', 'leiomyosarcoma of the vagina']",5283,,,C1336940,,C6326,,,,,,
mondo:0003370,retroperitoneal leiomyosarcoma,"['leiomyosarcoma of retroperitoneal space', 'retroperitoneal leiomyosarcoma', 'retroperitoneal space leiomyosarcoma']",5284,,,C2187547,,C27904,,,,,,
mondo:0003371,breast leiomyosarcoma,"['leiomyosarcoma of the breast', 'leiomyosarcoma of breast', 'breast leiomyosarcoma']",5285,,,C1332631,,C5186,,,,,,
mondo:0003372,vulvar leiomyosarcoma,"['mammalian vulva leiomyosarcoma', 'leiomyosarcoma of mammalian vulva']",5286,,,C2168304,,C40318,1001975,,,,,
mondo:0003373,kidney leiomyosarcoma,"['leiomyosarcoma of kidney', 'kidney leiomyosarcoma', 'leiomyosarcoma of the kidney', 'renal leiomyosarcoma']",5287,,,C1335743,,C6183,,,,,,
mondo:0003374,laryngeal leiomyosarcoma,"['laryngeal leiomyosarcoma', 'leiomyosarcoma of the larynx', 'leiomyosarcoma of larynx', 'larynx leiomyosarcoma']",5288,,,C1334371,,C6022,,,,,,
mondo:0003376,mediastinum leiomyosarcoma,"['mediastinum leiomyosarcoma', 'leiomyosarcoma of mediastinum', 'leiomyosarcoma of the mediastinum', 'mediastinal leiomyosarcoma']",5292,,,C1334660,,C6619,,,,,,
mondo:0003377,extrahepatic bile duct leiomyosarcoma,"['leiomyosarcoma of the bile duct', 'extrahepatic bile duct leiomyosarcoma', 'leiomyosarcoma of extrahepatic bile duct', 'leiomyosarcoma of the extrahepatic bile duct', 'leiomyosarcoma of bile duct', 'bile duct leiomyosarcoma']",5293,,,C1333508,,C5848,,,,,,
mondo:0003378,liver leiomyosarcoma,"['hepatic leiomyosarcoma', 'leiomyosarcoma of liver', 'leiomyosarcoma of the liver', 'liver leiomyosarcoma']",5296,,,C1333969,,C5756,,,,,,
mondo:0003379,rectum leiomyosarcoma,"['rectum leiomyosarcoma', 'leiomyosarcoma of rectum', 'leiomyosarcoma of the rectum', 'rectal leiomyosarcoma']",5297,,,C1335683,,C5549,,,,,,
mondo:0003381,pituitary gland disorder,"['pituitary gland disease or disorder', 'pituitary disease', 'pituitary gland disease', 'pituitary gland disorder', 'disease of pituitary gland', 'disorder of pituitary gland']",53,,,,,C26854,,D010900,253.9,,,
mondo:0003382,eyelid disorder,"['disease of eyelid', 'eyelid disease or disorder', 'disorder of eyelid', 'eyelid disorder', 'eyelid disease']",530,,,,,C26768,,D005141,374.9,H00,,
mondo:0003383,fallopian tube clear cell adenocarcinoma,"['fallopian tube clear cell carcinoma', 'clear cell adenocarcinoma of the fallopian tube', 'fallopian tube clear cell adenocarcinoma', 'clear cell carcinoma of the fallopian tube', 'clear cell carcinoma of fallopian tube', 'clear cell adenocarcinoma of fallopian tube']",5301,,,C1333591,,C6280,,,,,,
mondo:0003384,uterine ligament clear cell adenocarcinoma,['uterine ligament clear cell adenocarcinoma'],5302,,,C1519867,,C40139,,,,,,
mondo:0003386,bladder clear cell adenocarcinoma,"['clear cell adenocarcinoma of the urinary bladder', 'urinary bladder clear cell adenocarcinoma', 'clear cell adenocarcinoma of urinary bladder', 'bladder clear cell adenocarcinoma', 'clear cell adenocarcinoma of the bladder', 'bladder mesonephric adenocarcinoma', 'clear cell adenocarcinoma of bladder']",5306,,,C1332557,,C6179,,,,,,
mondo:0003387,urethra clear cell adenocarcinoma,"['clear cell adenocarcinoma of the urethra', 'urethra clear cell adenocarcinoma', 'clear cell adenocarcinoma of urethra', 'urethral clear cell adenocarcinoma']",5307,,,C1336886,,C6172,,,,,,
mondo:0003388,ampulla of vater clear cell adenocarcinoma,"['hepatopancreatic ampulla clear cell adenocarcinoma', 'ampulla of Vater clear cell adenocarcinoma']",5308,,,C1332246,,C27414,,,,,,
mondo:0003389,epithelial-myoepithelial carcinoma,"['EMYOCA', 'epithelial-myoepithelial carcinoma']",5309,,,C0334392,,C4199,,,,,,
mondo:0003390,glycogen-rich clear cell breast carcinoma,"['glycogen-rich carcinoma (morphologic abnormality)', 'glycogen-rich, clear cell breast carcinoma', 'glycogen-rich carcinoma']",5310,,,C1512224,,C40368,,,,,,
mondo:0003391,vulvar alveolar soft part sarcoma,,5313,,,C1520069,,C40320,,,,,,
mondo:0003392,fallopian tube germ cell tumor,"['fallopian tube germ cell tumor', 'fallopian tube germ cell neoplasm', 'fallopian tube germ cell cancer']",5324,,,C1517114,,C40130,,,,,,
mondo:0003393,thymus gland disorder,"['thymus disease or disorder', 'thymus disease', 'disease of thymus gland', 'Thymus disorder', 'disorder of thymus', 'disease of thymus']",533,,,C0154199,,C26962,,,254.9,,,
mondo:0003394,dental pulp disorder,"['disorder of pulp of tooth', 'dental pulp disease', 'disease of dental pulp', 'dental pulp disease or disorder', 'dental pulp disorder', 'pulp disorder', 'disorder of dental pulp']",5330,,,C0011405,,C34530,,D003788,522.9,,,
mondo:0003395,testicular granulosa cell tumor,"['granulosa cell tumor of testis', 'testicular granulosa cell neoplasm', 'granulosa cell tumor of the testis', 'testicular granulosa cell tumor', 'granulosa cell neoplasm of testis', 'granulosa cell neoplasm of the testis', 'testis granulosa cell tumor', 'granulosa cell tumour of the testis', 'testis granulosa cell tumour', 'granulosa cell tumour of testis']",5331,,,C1336709,,C6357,1000567,,,,,
mondo:0003396,epulis,"['gum polyp', 'polyp of gingiva', 'gingival polyp', 'polyp of gum', 'gingiva polyp', 'epulides', 'polyp of the gingiva', 'polyp of the gum']",5337,,,C0266919,,C3948,,,523.8,,,
mondo:0003397,gingival hypertrophy,['hypertrophy of gingivae'],5338,,,C0017567,,,,D005886,,,,
mondo:0003398,anterograde amnesia,,5340,,,,,,,D020324,,R41.1,,
mondo:0003399,pineal region yolk sac tumor,"['pineal region yolk Sac neoplasm', 'pineal body yolk sac tumour', 'yolk Sac tumour of pineal region', 'endodermal sinus tumour of pineal region', 'yolk Sac tumour of the pineal region', 'pineal endodermal sinus tumor', 'pineal endodermal sinus tumour', 'endodermal sinus tumour of the pineal region', 'endodermal sinus tumor of the pineal region', 'pineal region endodermal sinus tumor', 'endodermal sinus tumor of pineal region', 'pineal body yolk sac tumor', 'pineal region endodermal sinus tumour', 'pineal region endodermal sinus neoplasm', 'pineal endodermal sinus neoplasm', 'pineal region yolk sac tumor', 'yolk Sac tumor of pineal region', 'yolk Sac tumor of the pineal region']",5341,,,C1335420,,C6752,,,,,,
mondo:0003400,childhood endodermal sinus tumor,"['childhood endodermal sinus tumor', 'pediatric endodermal sinus neoplasm', 'childhood yolk Sac tumor', 'childhood yolk Sac neoplasm', 'paediatric endodermal sinus neoplasm', 'paediatric yolk Sac neoplasm', 'pediatric yolk Sac neoplasm', 'childhood yolk Sac tumour', 'paediatric yolk Sac tumour', 'childhood endodermal sinus neoplasm', 'pediatric yolk Sac tumor']",5342,,,C1333016,,C27364,,,,,,
mondo:0003401,central nervous system endodermal sinus tumor,"['central nervous system yolk Sac tumor', 'paediatric central nervous system yolk Sac neoplasm', 'central nervous system yolk Sac tumour', 'paediatric central nervous system yolk Sac tumour', 'childhood central nervous system yolk Sac tumour', 'pediatric central nervous system yolk Sac tumor', 'yolk Sac tumor of the CNS', 'central nervous system yolk sac tumor', 'childhood central nervous system endodermal sinus tumour', 'childhood central nervous system endodermal sinus neoplasm', 'pediatric central nervous system endodermal sinus neoplasm', 'yolk Sac tumour of the CNS', 'central nervous system endodermal sinus tumor', 'childhood central nervous system yolk Sac neoplasm', 'childhood central nervous system yolk Sac tumor', 'paediatric central nervous system endodermal sinus neoplasm', 'childhood central nervous system endodermal sinus tumor', 'pediatric central nervous system yolk Sac neoplasm', 'central nervous system yolk sac tumour']",5343,,,,,C6209,,,,,,
mondo:0003402,testicular yolk sac tumor,"['endodermal sinus tumour of testis', 'yolk Sac neoplasm of the testis', 'yolk sac tumour', 'testicular endodermal sinus neoplasm', 'testicular yolk sac tumor', 'endodermal sinus tumor of the testis', 'yolk Sac tumour of the testis', 'endodermal-sinus tumor', 'testis yolk sac tumor', 'yolk Sac tumour of testis', 'endodermal-sinus tumour', 'testicular endodermal sinus tumor', 'testicular endodermal sinus tumour', 'endodermal sinus tumour of the testis', 'endodermal sinus neoplasm of the testis', 'yolk Sac tumor of testis', 'endodermal sinus tumor of testis', 'testis yolk sac tumour', 'endodermal sinus neoplasm of testis', 'testicular yolk Sac neoplasm', 'Orchidoblastoma', 'yolk sac tumor', 'yolk Sac tumor of the testis', 'yolk Sac neoplasm of testis']",5344,,,C0279708,,C8000,1000574,,,,,
mondo:0003403,testicular non-seminomatous germ cell cancer,"['malignant non-seminomatous germ cell neoplasm of the testis', 'testicular germ cell tumor non-seminomatous, malignant', 'testicular non-seminomatous germ cell cancer', 'testicular non-seminomatous germ cell tumor, malignant', 'malignant testicular non-seminomatous germ cell tumor', 'malignant non-seminomatous germ cell tumour of testis', 'testicular non-seminomatous malignant germ cell neoplasm', 'malignant non-seminomatous germ cell tumor of testis', 'malignant non-seminomatous germ cell tumor of the testis', 'malignant non-seminomatous germ cell cancer of testis', 'malignant testicular non-seminomatous germ cell tumour', 'malignant non-seminomatous germ cell cancer of the testis', 'malignant non-seminomatous germ cell tumour of the testis', 'testicular germ cell tumour non-seminomatous, malignant', 'malignant non-seminomatous germ cell neoplasm of testis', 'malignant testicular non-seminomatous germ cell neoplasm']",5345,,,C1334625,,C5027,,,,,,
mondo:0003404,adult yolk sac tumor,"['yolk Sac tumor', 'adult endodermal sinus tumor', 'adult yolk Sac tumour', 'adult yolk Sac tumor', 'adult endodermal sinus tumour', 'yolk Sac tumour', 'yolk sac tumor of adults', 'yolk sac tumour of adults', 'adult yolk Sac neoplasm', 'adult endodermal sinus neoplasm']",5348,,,C1332221,,C27241,,,,,,
mondo:0003405,adult central nervous system germ cell tumor,"['adult CNS germ cell tumor', 'germ cell neoplasm of the adult central nervous system', 'germ cell neoplasm of the adult CNS', 'germ cell tumour of the adult central nervous system', 'germ cell tumor of adult central nervous system', 'germ cell tumour of adult CNS', 'central nervous system germ cell tumor of adults', 'central nervous system germ cell tumor', 'central nervous system adult germ cell tumour', 'germ cell tumor of the adult CNS', 'central nervous system adult germ cell tumor', 'adult CNS germ cell tumour', 'germ cell tumour of adult central nervous system', 'germ cell tumor of adult CNS', 'germ cell neoplasm of adult CNS', 'central nervous system germ cell tumour of adults', 'adult CNS germ cell neoplasm', 'germ cell tumor of the adult central nervous system', 'adult central nervous system germ cell tumor', 'germ cell neoplasm of adult central nervous system', 'central nervous system germ cell tumour', 'adult central nervous system germ cell neoplasm', 'germ cell tumour of the adult CNS']",5349,,,C0280796,,C6285,,,,,,
mondo:0003406,sleep-wake disorder,"['sleep-related neurogenic Tachypneas', 'short sleeper syndromes', 'sleep related neurogenic tachypnea', 'sleeper syndrome, short', 'short sleep phenotype', 'Tachypneas, sleep-related neurogenic', 'long sleeper syndrome', 'sleep disorder', 'syndrome, long sleeper', 'syndromes, long sleeper', 'disorder, sleep wake', 'tachypnea, sleep-related neurogenic', 'short sleeper syndrome', 'sleeper syndromes, long', 'syndrome, Subwakefullness', 'disorders, sleep', 'disorders, sleep wake', 'sleep disorders', 'Subwakefullness syndrome', 'non-organic sleep disorder', 'phenotypes, short sleep', 'sleep wake disorder', 'wake disorders, sleep', 'sleep phenotypes, short', 'sleeper syndrome, long', 'phenotype, short sleep', 'syndrome, short sleeper', 'Subwakefullness syndromes', 'syndromes, short sleeper', 'wake disorder, sleep', 'sleep-related neurogenic tachypnea', 'long sleeper syndromes', 'neurogenic Tachypneas, sleep-related', 'disorder, sleep', 'sleeper syndromes, short', 'short sleep phenotypes', 'syndromes, Subwakefullness', 'neurogenic tachypnea, sleep-related']",535,,,,,,0008568,D012893,307.49,G47,,
mondo:0003408,ovarian primitive germ cell tumor,['ovarian primitive germ cell tumor'],5351,,,C1518727,,C39986,,,,,,
mondo:0003409,colonic disorder,"['colon disorder', 'colon disease or disorder', 'disorder of colon', 'colon disease', 'disease of colon']",5353,,,C0009373,,,,D003108,,,,
mondo:0003410,Wolffian duct adenocarcinoma,"['cervical mesonephric adenocarcinoma', 'mesonephric duct adenocarcinoma', 'Wolffian duct adenocarcinoma']",5368,,,C1516419,,C40254,,,,,,
mondo:0003411,breast hemangiopericytoma,"['breast spindle cell tumour', 'breast hemangiopericytoma', 'breast spindle cell tumor']",5370,,,C1511313,,C40396,,,,,,
mondo:0003412,retroperitoneal hemangiopericytoma,['retroperitoneal space hemangiopericytoma'],5373,,,C1335777,,C5386,,,,,,
mondo:0003413,hair follicle neoplasm,"['hair follicle neoplasm (disease)', 'tumour of hair follicle', 'hair matrix tumour', 'neoplasm of the hair follicle', 'hair matrix tumor', 'hair matrix neoplasm', 'hair follicle tumour', 'neoplasm of hair follicle', 'hair follicle tumor', 'tumor of hair follicle', 'hair follicle neoplasm']",5375,,,C0859920,,C7367,,,,,,
mondo:0003414,skin pilomatrix carcinoma,"['Trichomatrical carcinoma', 'calcifying epitheliocarcinoma', 'pilomatrix carcinoma of the skin', 'pilomatrix carcinoma', 'matrical carcinoma', 'pilomatrix skin carcinoma', 'Pilomatrical carcinoma', 'invasive pilomatrixoma', 'pilomatricoma, malignant', 'malignant pilomatricoma', 'calcified epithelial carcinoma of Malherbe', 'pilomatrix carcinoma of skin']",5376,,499182,C0585475,,C4114,,,,,,
mondo:0003417,internuclear ophthalmoplegia,,538,,,C0152134,,,,,378.86,H51.2,,
mondo:0003419,Bartholin gland adenoma,"['Bartholin^s gland adenoma', 'Bartholin gland adenoma', 'major vestibular gland adenoma']",5382,,,C1511048,,C40299,,,,,,
mondo:0003420,bile duct cystadenoma,"['cystadenoma of bile duct', 'bile duct cystadenoma', 'bile duct cystadenoma (morphologic abnormality)', 'bile duct mucinous cystic neoplasm', 'cystadenoma of the bile duct']",5384,,,C0334285,,C4129,,,,,,
mondo:0003421,mixed cell adenoma,['mixed cell adenoma'],5385,,,C0334323,,C4157,,,,,,
mondo:0003422,lung adenoma,"['lung adenoma', 'adenoma of the lung', 'adenoma of lung', 'pulmonary adenoma']",5386,,,C0345964,,C4455,,,,,,
mondo:0003423,middle ear adenoma,"['adenoma of middle ear', 'adenoma of the middle ear', 'middle ear adenoma']",5387,,,C1334759,,C6834,,,,,,
mondo:0003424,oncocytic adenoma,"['follicular adenoma, oxyphilic cell', 'oncocytic adenoma', 'oncocytoma', 'oxyphilic adenoma']",5389,,,C1510502,,C3759,1001079,,,,,
mondo:0003425,ophthalmoplegia,"['oculomotor paralysis', 'total ophthalmoplegia']",539,,,,,,,D009886,378.56,,,
mondo:0003426,clear cell adenoma,"['clear cell adenoma', 'adenoma, clear cell, benign', 'clear cell adenoma (morphologic abnormality)']",5390,,,C0334315,,C4151,,,,,,
mondo:0003427,bronchus adenoma,"['papillary adenoma of type II pneumocytes', 'type II pneumocyte adenoma', 'adenoma, bronchial, benign', 'peripheral papillary tumor of type II pneumocytes', 'lung papillary adenoma', 'adenoma of bronchus', 'peripheral papillary tumour of type II pneumocytes', 'bronchus adenoma', 'adenoma of the bronchus', 'bronchial adenoma', 'bronchial adenoma NOS (morphologic abnormality)']",5391,,,C0149845,,C3494,,,,,,
mondo:0003428,brain hemangioma,"['brain hemangioma', 'brain angioma']",5393,,,C0238814,,C7739,,,,,,
mondo:0003429,functioning pituitary gland adenoma,"['functioning adenoma of pituitary', 'secreting pituitary adenoma', 'functioning pituitary gland adenoma', 'secretory adenoma of pituitary gland', 'secretory adenoma of the pituitary', 'secretory pituitary adenoma', 'functioning adenoma of pituitary gland', 'endocrine active pituitary adenoma', 'functioning pituitary gland adenoma (benign)', 'functioning pituitary adenoma', 'secretory adenoma of the pituitary gland', 'secretory pituitary gland adenoma', 'functioning adenoma of the pituitary', 'secretory adenoma of pituitary', 'functioning adenoma of the pituitary gland']",5395,,314753,C0854486,,C8388,,,,,,
mondo:0003430,prolactin producing pituitary tumor,"['prolactin secreting neoplasm of pituitary gland', 'prolactin secreting pituitary tumor', 'prolactin producing tumor of pituitary gland', 'prolactin secreting tumor of pituitary', 'prolactin secreting pituitary gland tumour', 'prolactin secreting tumor of pituitary gland', 'prolactin producing tumor of pituitary', 'prolactin secreting neoplasm of pituitary', 'prolactin producing pituitary tumor', 'prolactin-producing pituitary gland neoplasm', 'prolactin producing tumour of pituitary', 'prolactin-producing pituitary gland tumor', 'prolactin producing pituitary neoplasm', 'prolactin secreting pituitary gland neoplasm', 'prolactin producing tumour of the pituitary', 'prolactin producing tumor of the pituitary gland', 'prolactin producing tumor of the pituitary', 'PRL producing pituitary gland neoplasm', 'prolactin producing tumour of the pituitary gland', 'prolactin secreting tumour of the pituitary gland', 'prolactin secreting tumour of pituitary gland', 'prolactin secreting tumor of the pituitary', 'prolactin producing tumour of pituitary gland', 'malignant prolactinoma', 'prolactin secreting tumour of pituitary', 'prolactin secreting tumour of the pituitary', 'prolactin secreting neoplasm of the pituitary gland', 'prolactin producing pituitary gland tumour', 'prolactin secreting pituitary gland tumor', 'prolactin secreting tumor of the pituitary gland', 'prolactin producing neoplasm of the pituitary', 'prolactin producing pituitary gland neoplasm', 'malignant prolactin producing neoplasm of pituitary gland', 'prolactin producing neoplasm of the pituitary gland', 'prolactin producing neoplasm of pituitary', 'prolactin secreting pituitary tumour', 'prolactin secreting pituitary neoplasm', 'prolactin-producing pituitary gland tumour', 'prolactin producing neoplasm of pituitary gland', 'prolactin secreting neoplasm of the pituitary', 'prolactin producing pituitary gland tumor']",5396,,,C0278863,,C7910,,,,,,
mondo:0003431,lipoadenoma,"['lipoadenoma (morphologic abnormality)', 'lipoadenoma', 'adenolipoma, benign']",5398,,,C0334325,,C4159,,,,,,
mondo:0003432,strabismus,"['strabismus', 'squint']",540,,,C0038379,,C35040,,D013285,378.7,,,
mondo:0003433,water-clear cell adenoma,"['water-clear cell adenoma (morphologic abnormality)', 'parathyroid gland water-clear cell adenoma']",5401,,,C0334321,,C4155,,,,,,
mondo:0003434,vaginal adenoma,"['vaginal adenoma', 'vagina adenoma']",5402,,,C1519913,,C40256,,,,,,
mondo:0003435,microcystic adenoma,"['microcystic adenoma', 'microcystic adenoma (morphologic abnormality)']",5403,,,C0205648,,C3685,,,,,,
mondo:0003437,occult small cell lung carcinoma,"['occult small cell carcinoma of lung', 'occult small cell carcinoma of the lung', 'occult small cell lung carcinoma', 'lung occult small cell carcinoma']",5414,,,C1335099,,C6683,,,,,,
mondo:0003438,combined small cell lung carcinoma,"['combined type small cell carcinoma of the lung', 'combined small and large cell lung carcinoma', 'combined type small cell carcinoma of lung', 'mixed small cell and large cell carcinoma of the lung', 'small cell and large cell carcinoma of lung', 'small cell and large cell carcinoma of the lung', 'lung combined type small cell carcinoma', 'combined small cell carcinoma of lung', 'combined small cell lung carcinoma', 'combined small cell carcinoma of the lung', 'small cell and large cell lung carcinoma', 'combined type small cell lung carcinoma', 'mixed small cell and large cell carcinoma of lung', 'combined small cell and large cell lung carcinoma', 'mixed small cell and large cell lung carcinoma', 'combined small cell lung cancer', 'CSCLC', 'combined small and large cell lung cancer']",5421,,,C1333125,,C9137,,,,,,
mondo:0003439,urinary bladder villous adenoma,"['villous adenoma of the urinary bladder', 'urinary bladder villous adenoma', 'bladder villous adenoma', 'villous adenoma of urinary bladder']",5427,,,C1336893,,C7414,,,,,,
mondo:0003441,dystonic disorder,"['dystonia', 'dystonic disease', 'dystonia disorders', 'dystonia disorder', 'dystonic disorder']",543,,,,,C34563,,D020821,333.90,G24,,0001332
mondo:0003442,bladder papillary urothelial neoplasm,"['urinary bladder papillary urothelial neoplasm', 'bladder papillary transitional cell neoplasm', 'urinary bladder papillary transitional cell neoplasm', 'urinary bladder urothelium papillary epithelial neoplasm', 'bladder papillary urothelial neoplasm']",5432,,,C1511197,,C39857,,,,,,
mondo:0003443,papillary urothelial neoplasm,"['urothelium papillary epithelial neoplasm', 'urinary tract papillary transitional cell neoplasm', 'papillary transitional cell neoplasm of the urinary tract', 'urinary tract papillary transitional cell benign neoplasm', 'inverted papilloma of urinary tract', 'papillary urothelial neoplasm']",5433,,,C1335329,,C27883,,,,,,
mondo:0003444,intrahepatic bile duct adenoma,"['adenoma, HEPATOCHOLANGIOCELLULAR, benign', 'adenoma of the intrahepatic bile duct', 'intrahepatic bile duct adenoma', 'adenoma of intrahepatic bile duct']",5437,,,C1331535,,C7126,,,,,,
mondo:0003445,extrahepatic bile duct adenoma,"['adenoma of the extrahepatic bile duct', 'extrahepatic bile duct adenoma', 'adenoma of extrahepatic bile duct']",5438,,,C1331534,,C5857,,,,,,
mondo:0003446,papillary hidradenoma,['hidradenoma papilliferum'],5439,,,C0334348,,C4171,,,,,,
mondo:0003447,clear cell hidradenoma,"['clear cell myoepithelioma', 'clear cell hidradenoma (morphologic abnormality)', 'clear cell hidradenoma']",5443,,,C1370701,,C7567,,,,,,
mondo:0003448,benign spiradenoma,"['spiradenoma', 'spiroma/spiradenoma', 'benign eccrine spiradenoma', 'eccrine spiradenoma of skin', 'eccrine spiradenoma (morphologic abnormality)', 'eccrine spiradenoma']",5444,,,C0334347,,C4170,,,,,,
mondo:0003450,eccrine papillary adenoma,"['eccrine papillary adenoma of skin', 'Papillary eccrine adenoma']",5446,,,C0334350,,C4173,,,,,,
mondo:0003452,cochlear disorder,"['cochlea disease or disorder', 'cochlea disease', 'disorder of cochlea', 'disease of cochlea']",5463,,,C0009197,,,,D015834,,,,
mondo:0003453,conjunctival intraepithelial neoplasm,"['intraepithelial neoplasia of conjunctiva', 'conjunctiva intraepithelial neoplasia', 'intraepithelial neoplasia of the conjunctiva', 'conjunctival intraepithelial neoplasia']",5465,,,C1333148,,C6120,,,239.89,,,
mondo:0003454,conjunctival cancer,"['malignant neoplasm of conjunctiva', 'malignant neoplasm of the conjunctiva', 'malignant tumour of conjunctiva', 'malignant conjunctiva tumor', 'malignant tumour of the conjunctiva', 'malignant conjunctival neoplasm', 'conjunctiva cancer', 'malignant conjunctiva tumour', 'malignant tumor of the conjunctiva', 'malignant conjunctival tumour', 'malignant tumor of conjunctiva', 'cancer of conjunctiva', 'malignant conjunctival tumor', 'conjunctival tumour', 'malignant conjunctiva neoplasm', 'malignant neoplasm of conjunctiva (primary)', 'conjunctival tumor']",5467,,,,,C3564,,,190.3,,,
mondo:0003455,bile duct papillary neoplasm,"['IPN', 'bile duct papillary epithelial neoplasm', 'biliary papillomatosis', 'bile duct papillomatosis', 'intraductal papillary neoplasm', 'bile duct papillary neoplasm']",5468,,,C1879344,,C6881,,,,,,
mondo:0003458,uterine corpus adenofibroma,"['uterine body adenofibroma', 'adenofibroma of the corpus uteri', 'adenofibroma of body of uterus', 'body of uterus adenofibroma', 'adenofibroma of uterine corpus', 'adenofibroma of the uterine body', 'adenofibroma of the body of uterus', 'adenofibroma of corpus uteri', 'adenofibroma of the uterine corpus', 'adenofibroma of uterine body', 'corpus uteri adenofibroma']",5475,,,C1336901,,C6337,,,,,,
mondo:0003459,cervical adenofibroma,,5476,,,C1516402,,C40230,,,,,,
mondo:0003460,clear cell adenofibroma,"['clear cell adenofibroma', 'clear cell adenofibroma (morphologic abnormality)']",5477,,,,,C8987,,D062625,,,,
mondo:0003461,fallopian tube serous adenofibroma,"['serous adenofibroma of fallopian tube', 'fallopian tube serous adenofibroma', 'fallopian tube adenofibroma']",5478,,,C1517109,,C40113,,,,,,
mondo:0003462,papillary adenofibroma,['papillary adenofibroma'],5479,,,C1377850,,C8986,,,,,,
mondo:0003463,ovarian endometrioid adenofibroma,['ovarian endometrioid adenofibroma'],5480,,,C2212024,,C27287,,,,,,
mondo:0003464,cystadenofibroma,['cystadenofibroma'],5482,,,,,C8987,,D062625,,,,
mondo:0003465,fibrous synovial sarcoma,"['fibrous sarcoma of the synovium', 'fibrous sarcoma of synovium']",5484,,,C1333616,,C6533,,,,,,
mondo:0003466,spindle cell synovial sarcoma,"['synovial sarcoma, monophasic fibrous', 'synovial sarcoma with spindle cell components']",5487,,,C0334505,,C4277,,,,,,
mondo:0003467,mediastinum synovial sarcoma,"['mediastinal synovial sarcoma', 'synovial sarcoma of mediastinum', 'mediastinum synovial sarcoma (disease)', 'synovial sarcoma of the mediastinum']",5488,,,C1334681,,C6618,,,,,,
mondo:0003468,biphasic synovial sarcoma,"['synovial sarcoma, biphasic', 'biphasic sarcoma of synovium', 'biphasic sarcoma of the synovium', 'synovial sarcoma, biphasic (morphologic abnormality)']",5492,,,C0334507,,C4279,,,,,,
mondo:0003469,epithelioid cell synovial sarcoma,"['epithelioid cell sarcoma of synovium', 'epithelial sarcoma of synovium', 'synovial sarcoma, epithelioid cell', 'epithelioid cell sarcoma of the synovium', 'epithelial synovial sarcoma', 'synovial sarcoma, epithelioid cell (morphologic abnormality)', 'epithelioid synovial sarcoma', 'epithelial sarcoma of the synovium']",5494,,,C0334506,,C4278,,,,,,
mondo:0003470,cellular ependymoma,,5500,,,C1384403,,C4714,,,,,,
mondo:0003471,Pediculus humanus capitis infestation,"['Pediculus capitis infestation', 'infections, Pediculus humanus capitis', 'Pediculus humanus capitis infection', 'head louse infestation', 'pediculosis capitis', 'Pediculus capitis [head louse]', 'Pediculus capitis']",5501,,,C0030757,,,,,132.0,,,
mondo:0003472,lice infestation,"['mixed pediculosis', 'mixed pediculosis infestation', 'louse infestation', 'infections, Pediculus humanus', 'infestation by Pediculus', 'pediculosis + lice', 'pediculosis and Phthirus infection', 'pediculosis and Phthirus infections', 'pediculosis, unspecified', 'louse infestation (& [pediculosis and Phthirus] or [lice])', 'pediculosis', 'Pediculus humanus infection', 'pediculosis and Phthirus infestation']",5502,,,C0277351,,C128401,,D010373,132.9,B85.2,,
mondo:0003473,spinal cord ependymoma,"['ependymoma of the spinal cord', 'spinal cord ependymoma', 'ependymoma of spinal cord', 'ependymal neoplasm of the spinal cord']",5503,,,C0238432,,C3875,,,,,,
mondo:0003474,tanycytic ependymoma,['tanycytic ependymoma'],5504,,,C1370500,,C6903,,,,,,
mondo:0003475,papillary ependymoma,['papillary ependymoma'],5505,,,C0334578,,C4319,,,,,,
mondo:0003476,clear cell ependymoma,['clear cell ependymoma'],5507,,,,,C4714,,,,,,
mondo:0003477,brain stem ependymoma,"['ependymoma of the brain stem', 'ependymoma of brainstem', 'ependymoma of brain stem', 'ependymoma of the brainstem', 'brain stem ependymoma', 'brainstem ependymoma']",5508,,,C1332609,,C5098,,,,,,
mondo:0003478,childhood ependymoma,"['pediatric ependymoma', 'ependymoma of childhood', 'paediatric ependymoma', 'childhood ependymoma', 'ependymoma']",5509,,,,,C8578,,C531673,,,,
mondo:0003479,toxic pneumonitis,"['acute chemical fume pulmonary edema', 'acute chemical fume pulmonary oedema', 'acute chemical pulmonary oedema', 'acute chemical pulmonary edema']",551,,,C3714582,,,,,506.9,,,
mondo:0003480,pineal region dysgerminoma,"['pineal body dysgerminoma (disease)', 'pineal region dysgerminoma', 'pineal dysgerminoma']",5510,,,C1335415,,C7169,,,,,,
mondo:0003481,dysgerminoma of ovary,"['dysgerminoma of the ovary', 'dysgerminoma of ovary', 'ovarian dysgerminoma', 'ovarian germ cell dysgerminoma', 'germ cell dysgerminoma of the ovary', 'dysgerminoma', 'ovary dysgerminoma (disease)', 'germ cell dysgerminoma of ovary']",5511,,,C0346185,,C8106,1000414,,,,,
mondo:0003482,Pediculus humanus corporis infestation,"['Pediculus corporis', 'Pediculus humanus corporis infection', 'Pediculus corporis [body louse]', 'body louse infestation', 'infections, Pediculus humanus corporis', 'Pediculus humanus infestation']",5513,,,C0030758,,,,,132.1,,,
mondo:0003486,basaloid squamous cell carcinoma,"['basaloid carcinoma (morphologic abnormality)', 'basaloid squamous cell carcinoma (morphologic abnormality)', 'basaloid carcinoma', 'basaloid squamous cell carcinoma']",5522,,,C1266005,,C54244,,,,,,
mondo:0003487,pseudoglandular squamous cell carcinoma,"['adenoid squamous cell carcinoma', 'pseudoglandular epidermoid carcinoma', 'pseudoglandular squamous carcinoma', 'pharyngeal tonsil squamous cell carcinoma', 'acantholytic squamous cell carcinoma', 'adenoacanthoma', 'pseudoglandular epidermoid cell carcinoma', 'adenocarcinoma with squamous metaplasia', 'adenoid squamous cell carcinoma (morphologic abnormality)', 'pseudoglandular squamous cell carcinoma', 'adenoid squamous carcinoma', 'adenocarcinoma with squamous metaplasia (morphologic abnormality)']",5524,,,C0334393,,C4106,,,,,,
mondo:0003490,ampulla of vater squamous cell carcinoma,"['hepatopancreatic ampulla squamous cell carcinoma', 'ampulla of Vater squamous cell carcinoma']",5527,,,C1332251,,C27417,,,,,,
mondo:0003492,lacrimal gland squamous cell carcinoma,"['epidermoid carcinoma of lacrimal gland', 'squamous cell carcinoma of the lacrimal gland', 'epidermoid carcinoma of the lacrimal gland', 'lacrimal gland squamous cell carcinoma', 'squamous cell carcinoma of lacrimal gland', 'lacrimal gland epidermoid carcinoma']",5529,,,C1334360,,C6092,,,,,,
mondo:0003493,thymus squamous cell carcinoma,"['squamous cell carcinoma of Thymus', 'thymic squamous cell carcinoma', 'thymus squamous cell carcinoma', 'epidermoid thymic carcinoma', 'squamous cell carcinoma of the Thymus', 'Thymus squamous cell carcinoma']",5530,,,C1336082,,C6455,1000579,,,,,
mondo:0003494,ovarian squamous cell carcinoma,"['ovarian squamous cell cancer', 'ovary squamous cell carcinoma', 'ovarian squamous cell carcinoma']",5531,,,C2019443,,C40093,1000432,,,,,
mondo:0003495,ovarian squamous cell neoplasm,"['ovarian squamous cell tumour', 'ovarian squamous cell tumor', 'ovarian squamous cell neoplasm', 'ovary squamous cell neoplasm']",5532,,,C1518739,,C40092,,,,,,
mondo:0003497,renal pelvis squamous cell carcinoma,"['squamous cell carcinoma of renal pelvis', 'kidney renal pelvis squamous cell cancer', 'epidermoid carcinoma of renal pelvis', 'epidermoid carcinoma of the renal pelvis', 'epidermoid carcinoma of kidney pelvis', 'squamous cell carcinoma of kidney pelvis', 'kidney pelvis epidermoid carcinoma', 'renal pelvis epidermoid carcinoma', 'squamous cell carcinoma of the kidney pelvis', 'renal pelvis squamous cell carcinoma', 'squamous cell carcinoma of the renal pelvis', 'epidermoid carcinoma of the kidney pelvis', 'kidney pelvis squamous cell carcinoma', 'renal pelvis squamous cell cancer']",5534,,,C0238409,,C7732,,,,,,
mondo:0003499,sarcomatoid squamous cell skin carcinoma,"['spindle cell squamous cell carcinoma', 'spindle cell squamous carcinoma of the skin', 'spindle cell squamous carcinoma of skin', 'spindle cell (sarcomatoid) squamous cell skin carcinoma', 'spindle cell (sarcomatoid) squamous cell carcinoma']",5536,,,C0349656,,C4666,,,,,,
mondo:0003500,squamous cell bile duct carcinoma,['bile duct squamous cell carcinoma'],5537,,,C0861861,,C5777,,,,,,
mondo:0003501,external ear squamous cell carcinoma,"['squamous cell carcinoma of the external Ear', 'squamous cell carcinoma of external Ear', 'epidermoid carcinoma of external Ear', 'epidermoid carcinoma of the external Ear', 'external ear squamous cell carcinoma', 'external Ear squamous cell carcinoma', 'epidermoid carcinoma of the external ear', 'squamous cell carcinoma of external ear', 'external Ear epidermoid carcinoma']",5538,,,C1333494,,C6083,,,,,,
mondo:0003502,ureter squamous cell carcinoma,"['ureteral epidermoid carcinoma', 'ureteral squamous cell carcinoma', 'epidermoid carcinoma of the ureter', 'ureter squamous cell carcinoma', 'squamous cell carcinoma of ureter', 'ureter epidermoid carcinoma', 'squamous cell carcinoma of the ureter', 'epidermoid carcinoma of ureter']",5539,,,C1336879,,C6154,,,,,,
mondo:0003503,fallopian tube squamous cell carcinoma,"['fallopian tube squamous cell cancer', 'squamous cell carcinoma of fallopian tube', 'fallopian tube squamous cell carcinoma', 'squamous cell carcinoma of the fallopian tube']",5540,,,C1333596,,C6282,,,,,,
mondo:0003504,anal canal neuroendocrine neoplasm,"['anal neuroendocrine neoplasm', 'anal neuroendocrine tumor', 'anus neuroendocrine tumour', 'anal neuroendocrine tumour', 'neuroendocrine neoplasm of anus', 'neuroendocrine neoplasm of the anus', 'neuroendocrine neoplasm of anal canal', 'anus neuroendocrine tumor', 'neuroendocrine tumor of anus', 'neuroendocrine tumour of anus', 'anal canal neuroendocrine tumor, well differentiated, low or intermediate grade', 'anal canal neuroendocrine tumour', 'anal canal neuroendocrine tumor', 'anus neuroendocrine neoplasm', 'anal canal neuroendocrine neoplasm', 'anal canal NET']",5545,,,,,C5603,,,,,,
mondo:0003505,femoral cancer,"['malignant femur neoplasm', 'malignant neoplasm of femur', 'cancer of femur', 'neoplasm of femur', 'femur cancer', 'femoral neoplasm']",5546,,,,,,0007270,D005266,,,,
mondo:0003506,pulmonary artery choriocarcinoma,"['pulmonary artery chorioepithelioma', 'syncytioma of the pulmonary artery', 'syncytioma of pulmonary artery', 'pulmonary artery choriocarcinoma (disease)', 'pulmonary artery choriocarcinoma', 'choriocarcinoma of pulmonary artery', 'chorioepithelioma of pulmonary artery', 'choriocarcinoma of the pulmonary artery', 'pulmonary artery syncytioma', 'chorioepithelioma of the pulmonary artery']",5547,,,C1335571,,C5381,,,,,,
mondo:0003507,choriocarcinoma of ovary,"['choriocarcinoma of the ovary', 'ovarian germ cell choriocarcinoma', 'ovary choriocarcinoma (disease)', 'choriocarcinoma of ovary', 'ovarian choriocarcinoma', 'germ cell choriocarcinoma of ovary', 'germ cell choriocarcinoma of the ovary']",5550,,,C0346181,,C4515,1000413,,,,,
mondo:0003508,choriocarcinoma of testis,"['testis choriocarcinoma (disease)', 'choriocarcinoma of the testis', 'choriocarcinoma of testis', 'testicular choriocarcinoma', 'choriocarcinoma']",5551,,,C0238449,,C7733,1000564,,,,,
mondo:0003509,pineal region choriocarcinoma,"['choriocarcinoma of pineal region', 'pineal area choriocarcinoma', 'choriocarcinoma of the pineal area', 'choriocarcinoma of the pineal region', 'pineal choriocarcinoma', 'choriocarcinoma of pineal area']",5553,,,C1335414,,C6759,,,,,,
mondo:0003510,malignant testicular germ cell tumor,"['testicular germ cell cancer', 'malignant testicular germ cell tumor', 'malignant germ cell neoplasm of the testis', 'testicular ca. (no germ/tropho.)', 'malignant germ cell tumour of testis', 'malignant germ cell tumour of the testis', 'malignant testicular germ cell neoplasm', 'testicular malignant germ cell cancer', 'malignant germ cell neoplasm of testis', 'testicular cancer (excluding germ cell or trophoblastic cancer)', 'malignant germ cell tumor of testis', 'testicular cancer', 'malignant germ cell tumor of the testis']",5556,,,C0855197,,C9063,,,186.9,,,
mondo:0003512,mediastinal mesenchymal tumor,"['mediastinal soft tissue neoplasm', 'soft tissue neoplasm of mediastinum', 'soft tissue tumour of mediastinum', 'soft tissue neoplasm of the mediastinum', 'soft tissue tumor of the mediastinum', 'mediastinal soft tissue tumor', 'soft tissue tumour of the mediastinum', 'soft tissue tumor of mediastinum', 'mediastinal soft tissue tumour']",5560,,,C1334669,,C6637,,,,,,
mondo:0003513,gastric teratoma,"['stomach teratoma', 'teratoma of the stomach', 'teratoma of stomach', 'gastric teratoma']",5561,,,C1333790,,C5259,,,,,,
mondo:0003514,malignant teratoma,"['malignant extragonadal teratoma', 'teratoma, malignant']",5563,,,C0855163,,C8884,,,,,,
mondo:0003515,fallopian tube teratoma,['fallopian tube teratoma'],5564,,,C1517127,,C40131,,,,,,
mondo:0003516,adult teratoma,"['teratoma of adults', 'teratoma', 'adult teratoma']",5565,,,C1368898,,C9013,,,,,,
mondo:0003517,mature teratoma,['mature teratoma'],5566,,,C1368910,,C9015,,,,,,
mondo:0003518,mediastinum teratoma,"['mediastinum teratoma', 'teratoma of mediastinum']",5568,,,C1334682,,C6438,,,,,,
mondo:0003519,malignant syringoma,"['syringoma, malignant', 'syringomatous carcinoma', 'microcystic adnexal carcinoma', 'MAC', 'microcystic adnexal carcinoma of skin']",5569,,,C0346027,,C7581,,,,,,
mondo:0003522,male orgasm disorder,"['inhibited male orgasm', 'male orgasmic disorder']",5576,,,,,C34959,,,,F52.32,,
mondo:0003523,gastrin-producing neuroendocrine tumor,"['G cell tumor', 'G cell tumour', 'gastrinoma', 'gastrin-producing NET', 'gastrin secreting tumor', 'gastrin-producing neuroendocrine tumor', 'G-cell tumour', 'gastrin cell tumor', 'G-cell tumor', 'gastrin cell tumour', 'malignant gastrinoma', 'G-cell gastrin producing tumor', 'G-cell gastrin producing tumour', 'gastrin secreting tumour']",5577,,,CN206461,,C3050,,,,,,
mondo:0003524,gastric gastrin-producing neuroendocrine tumor,"['gastric G-cell gastrin producing tumour', 'gastrin producing tumour of the stomach', 'gastrin-producing neuroendocrine tumor of stomach', 'gastrin-producing neuroendocrine tumor of the stomach', 'gastric gastrin-producing NET', 'gastrin-producing neuroendocrine tumour of stomach', 'gastrin-producing neuroendocrine tumour of the stomach', 'gastric gastrinoma', 'gastric gastrin producing tumor', 'gastric gastrin producing tumour', 'gastrin producing neuroendocrine tumor of the stomach', 'stomach gastrin-producing neuroendocrine tumour', 'stomach gastrin-producing neuroendocrine tumor', 'gastric gastrin-producing neuroendocrine tumor', 'gastric G-cell gastrin producing tumor', 'gastrin producing neuroendocrine tumour of the stomach', 'gastrin producing tumor of the stomach']",5579,,,C1333767,,C27444,,,,,,
mondo:0003525,pancreatic gastrin-producing neuroendocrine tumor,"['gastrin-producing neuroendocrine tumor of pancreas', 'pancreas gastrin-producing neuroendocrine tumor', 'pancreatic G-cell tumour', 'islet cell tumor, ulcerogenic', 'pancreatic gastrin producing tumour', 'pancreatic G-cell tumor', 'pancreatic gastrin producing NET', 'gastrin-producing neuroendocrine tumour of pancreas', 'pancreatic gastrin producing tumor', 'pancreas gastrin-producing neuroendocrine tumour', 'pancreatic gastrin-producing neuroendocrine tumor']",5580,,,C1368066,,C9069,,D015408,,,,
mondo:0003528,Volkmann contracture,"['Volkmann^s ischemic contracture', 'Volkmann^s ischaemic contracture']",5587,,,C0042951,,C35130,,D054061,958.6,,,
mondo:0003529,acute pyelonephritis,"['pyelonephritis, acute']",559,,,C0520575,,C123215,,,590.1,N10,,
mondo:0003530,aggressive digital papillary adenocarcinoma,,5590,,,,,,,,,,,
mondo:0003531,papillary eccrine carcinoma,"['digital papillary adenocarcinoma', 'papillary apocrine fibroadenoma', 'papillary eccrine carcinoma', 'eccrine papillary adenocarcinoma', 'tubular apocrine adenoma', 'papillary eccrine adenoma']",5591,,,C1367774,,C27254,,,,,,
mondo:0003532,breast papillary carcinoma,"['solid papillary carcinoma of the breast', 'papillary carcinoma of the breast', 'breast papillary carcinoma', 'papillary breast carcinoma', 'Papillary breast cancer', 'papillary carcinoma of breast', 'breast solid papillary carcinoma']",5592,,,C3812899,,C9134,,,,,,
mondo:0003534,papillary thymic adenocarcinoma,"['papillary carcinoma of Thymus', 'Thymus papillary carcinoma', 'papillary carcinoma of the Thymus', 'thymic papillary carcinoma', 'thymic papillary adenocarcinoma', 'thymus papillary adenocarcinoma']",5595,,,C1335327,,C27937,,,,,,
mondo:0003535,fallopian tube papillary adenocarcinoma,"['papillary adenocarcinoma of the fallopian tube', 'fallopian tube papillary adenocarcinoma', 'papillary adenocarcinoma of fallopian tube']",5597,,,C1333595,,C6267,,,,,,
mondo:0003537,precursor T-lymphoblastic lymphoma/leukemia,"['precursor T lymphoblastic lymphoma/leukemia', 'precursor T-lymphoblastic lymphoma/leukemia', 'T lymphoblastic leukemia/lymphoma', 'precursor T lymphoblastic leukemia/lymphoma']",5599,,,C1301359,,C8694,,,,,,
mondo:0003538,precursor lymphoblastic lymphoma/leukemia,"['precursor lymphoblastic leukemia/lymphoma', 'precursor lymphoid neoplasm', 'precursor lymphoblastic lymphoma/leukemia']",5600,,,C1335469,,C7055,0009119,,,,,
mondo:0003539,T-cell adult acute lymphocytic leukemia,"['acute Adult T-cell Leukemia-lymphoma', 'T cell adult acute lymphocytic leukaemia', 'T cell adult acute lymphoblastic leukemia', 'adult T acute lymphoblastic leukaemia', 'T Acute Lymphoblastic Leukemia', 'adult acute lymphoblastic leukaemia of T cell', 'adult T-cell acute lymphoblastic leukemia', 'adult precursor T-lymphoblastic leukemia', 'adult T-cell acute lymphoblastic leukaemia', 'adult precursor T lymphoblastic leukemia', 'adult acute lymphoblastic leukemia of T cell', 'adult precursor T-lymphoblastic leukaemia', 'T cell adult acute lymphocytic leukemia', 'T cell adult acute lymphoblastic leukaemia', 'T-cell adult ALL', 'adult T acute lymphoblastic leukemia', 'adult precursor T lymphoblastic leukaemia', 'T Acute Lymphoblastic Leukaemia', 'T cell adult ALL']",5602,,,C0279592,,C9142,1001936,,,,,
mondo:0003540,acute T cell leukemia,"['precursor T lymphoblastic leukaemia', 'T-cell acute lymphoblastic leukaemia', 'precursor T lymphoblastic leukemia']",5603,,,C0023493,,C3184,,,,,,
mondo:0003541,adult acute lymphoblastic leukemia,"['adult acute lymphoid leukaemia', 'adult acute lymphoblastic leukemia', 'adult ALL', 'acute lymphoblastic leukemia (ALL)', 'adult precursor lymphoblastic leukemia', 'adult acute lymphocytic leukaemia', 'adult acute lymphocytic leukemia', 'adult acute lymphoid leukemia', 'acute lymphoblastic leukaemia (ALL)', 'adult acute lymphogenous leukemia', 'adult precursor lymphoblastic leukaemia', 'adult acute lymphogenous leukaemia']",5604,,,C0751606,,C4967,,,,,,
mondo:0003542,dental pulp calcification,"['pulp calcifications', 'pulpal calcifications', 'pulp calcification']",5608,,,C0011401,,,,D003784,,K04.2,,
mondo:0003543,trigeminal nerve disorder,"['trigeminal nerve disease', 'disorder of trigeminal nerve', 'trigeminal nerve disease or disorder', 'disease of trigeminal nerve']",561,,,,,C26952,,D020433,350.8,,,
mondo:0003544,spinal cord cancer,"['malignant spinal cord tumor', 'malignant spinal cord tumour', 'malignant tumour of spinal cord', 'malignant neoplasm of the spinal cord', 'tumor of the spinal cord', 'spinal cord cancer', 'spinal cord neoplasm', 'malignant tumour of the spinal cord', 'spinal neoplasm', 'spinal cancer', 'tumour of the spinal cord', 'cancer of spinal cord', 'spine cancer', 'malignant neoplasm of spinal cord', 'malignant tumor of spinal cord', 'malignant tumor of the spinal cord', 'intraspinal tumor', 'intraspinal tumour', 'malignant spinal cord neoplasm']",5612,,,C0153646,,C3572,,,192.2,C72.0,,
mondo:0003545,intradural extramedullary spinal canal neoplasm,"['intradural extramedullary spinal tumours', 'intradural extramedullary spinal canal tumor', 'intradural extramedullary spinal tumors', 'intradural extramedullary tumour of spinal canal', 'intradural extramedullary neoplasm of the spinal canal', 'intradural extramedullary neoplasm of spinal canal', 'intradural extramedullary tumor of the spinal canal', 'intradural extramedullary spinal canal tumors', 'intradural extramedullary spinal canal neoplasm', 'intradural extramedullary tumor of spinal canal', 'intradural extramedullary spinal neoplasms', 'intradural extramedullary spinal canal tumours', 'spinal canal intradural extramedullary neoplasm', 'intradural extramedullary spinal canal tumour', 'intradural extramedullary tumour of the spinal canal']",5615,,,C1334255,,C5135,,,,,,
mondo:0003546,third cranial nerve disorder,"['disorder of oculomotor nerve', 'oculomotor nerve disorder', 'oculomotor nerve disease or disorder', 'oculomotor nerve disease', 'disease of oculomotor nerve']",562,,,C0271353,,C27598,,D015840,,,,
mondo:0003548,adenosquamous breast carcinoma,"['breast adenosquamous carcinoma', 'adenosquamous breast carcinoma', 'metaplastic adenosquamous carcinoma']",5623,,,C1510796,,C40361,,,,,,
mondo:0003549,adenosquamous bile duct carcinoma,"['adenosquamous carcinoma of the bile duct', 'adenosquamous bile duct carcinoma', 'adenosquamous carcinoma of bile duct', 'bile duct adenosquamous carcinoma']",5624,,,C0861854,,,,,,,,
mondo:0003550,esophageal adenosquamous carcinoma,"['esophageal adenosquamous cancer', 'oesophagus adenosquamous carcinoma', 'esophagus adenosquamous carcinoma', 'esophageal adenosquamous carcinoma']",5625,,,C2063886,,C27421,,,,,,
mondo:0003551,thymic adenosquamous carcinoma,"['adenosquamous carcinoma of Thymus', 'thymus adenosquamous carcinoma', 'Thymus adenosquamous carcinoma', 'adenosquamous carcinoma of the Thymus', 'thymic adenosquamous carcinoma']",5626,,,C1332171,,C6458,,,,,,
mondo:0003553,ampulla of vater adenosquamous carcinoma,"['ampulla of Vater adenosquamous carcinoma', 'hepatopancreatic ampulla adenosquamous carcinoma']",5628,,,C1332245,,C27418,,,,,,
mondo:0003554,adenosquamous colon carcinoma,"['colon adenosquamous cancer', 'adenosquamous carcinoma of the colon', 'adenosquamous carcinoma of colon', 'colon adenosquamous carcinoma', 'colonic adenosquamous carcinoma', 'adenosquamous colon carcinoma']",5629,,,C1333082,,C5491,,,,,,
mondo:0003555,Bartholin gland adenosquamous carcinoma,"['major vestibular gland adenosquamous carcinoma', 'Bartholin^s gland adenosquamous carcinoma', 'Bartholin gland adenosquamous carcinoma']",5630,,,C1511050,,C40296,,,,,,
mondo:0003556,endometrial adenosquamous carcinoma,"['endometrial adenosquamous cancer', 'adenosquamous carcinoma of the endometrium', 'endometrium adenosquamous carcinoma', 'adenosquamous carcinoma of endometrium', 'endometrial adenosquamous carcinoma']",5631,,,C3896969,,C114656,1001952,,,,,
mondo:0003557,optic nerve sheath meningioma,"['meningioma of the optic nerve sheath', 'meningioma of optic nerve sheath', 'optic nerve sheath meningioma']",5632,,,C0346328,,C4538,,,237.9,,,
mondo:0003558,adenosquamous prostate carcinoma,"['prostate gland adenosquamous carcinoma', 'adenosquamous carcinoma of prostate', 'prostate adenosquamous carcinoma', 'adenosquamous carcinoma of the prostate']",5634,,,C1335503,,C5538,,,,,,
mondo:0003561,malignant giant cell tumor of soft parts,"['malignant giant cell neoplasm of soft parts', 'malignant Osteoclastoma', 'malignant giant cell tumor of soft parts', 'malignant giant cell tumor of soft parts (morphologic abnormality)', 'undifferentiated pleomorphic sarcoma with osteoclast-like giant cells', 'giant cell malignant fibrous histiocytoma', 'malignant giant cell tumour of soft parts (morphologic abnormality)', 'giant cell fibrous histiocytoma']",5638,,,C0334554,,C8380,,,,,,
mondo:0003562,rete testis neoplasm,"['tumour of rete testis', 'rete testis tumor', 'tumor of rete testis', 'rete testis neoplasm', 'rete testis neoplasm (disease)', 'neoplasm of rete testis', 'rete testis tumour']",5639,,,C1514912,,C39955,,,,,,
mondo:0003563,diffuse pulmonary fibrosis,,5641,,,C0865849,,C27216,,,,,,
mondo:0003564,localized pulmonary fibrosis,,5642,,,C0340127,,C27103,,,,,,
mondo:0003565,urethral villous adenoma,"['urethra villous adenoma', 'urethral villous adenoma']",5643,,,C1519828,,C39872,,,,,,
mondo:0003567,bilateral hypoactive labyrinth,"['hypoactive bilateral labyrinthine dysfunction', 'hypoactive labyrinth, bilateral']",565,,,C0155518,,,,,386.54,,,
mondo:0003568,disorder of optic chiasm,"['disorder of optic chiasma', 'chiasmal syndrome', 'disorder of optic chiasm', 'disease of optic chiasma', 'optic chiasma disease or disorder', 'chiasma syndrome']",5655,,,C0155307,,,,,377.63,H47.4,,
mondo:0003569,cranial nerve neuropathy,"['cranial nerve disorder', 'cranial neuropathy', 'disorder of cranial nerve', 'cranial nerve disease', 'disease of cranial neuron projection bundle', 'cranial neuron projection bundle disease', 'cranial neuron projection bundle disease or disorder', 'disorder of cranial neuron projection bundle']",5656,,,C0010266,,C26733,,D003389,352.9,,,
mondo:0003570,lipid-rich carcinoma,"['lipid-rich carcinoma (morphologic abnormality)', 'lipid-rich carcinoma']",5658,,,C0334318,,C4152,,,,,,
mondo:0003572,nasopharyngeal type undifferentiated carcinoma,"['Schmincke tumor', 'lymphoepithelial carcinoma', 'Schmincke tumour', 'Schminke tumour', 'lymphoepithelioma', 'lymphoepithelioma-like carcinoma', 'Schminke tumor', 'nasopharyngeal type undifferentiated carcinoma']",5660,,,C0334254,,C4107,,,,,,
mondo:0003573,pleomorphic carcinoma,"['pleomorphic carcinoma (morphologic abnormality)', 'pleomorphic carcinoma']",5662,,,C0334233,,C4094,,,,,,
mondo:0003574,external ear cancer,"['malignant external Ear neoplasm', 'malignant external Ear tumour', 'malignant tumour of the external Ear', 'malignant neoplasm of the external Ear', 'malignant neoplasm of external ear', 'external ear cancer', 'malignant neoplasm of the external ear', 'malignant tumor of external Ear', 'malignant external ear neoplasm', 'malignant tumor of the external Ear', 'cancer of external ear', 'malignant tumour of external Ear', 'malignant neoplasm of external Ear', 'malignant external Ear tumor']",5665,,,C0349576,,C4653,,,,,,
mondo:0003575,comedocarcinoma,"['Comedocarcinoma', 'comedo carcinoma']",5670,,,C0334370,,C4188,,,,,,
mondo:0003578,extragonadal nonseminomatous germ cell tumor,"['malignant neoplasm of the extragonadal non-seminomatous germ cell', 'malignant tumor of extragonadal non-seminomatous germ cell', 'malignant extragonadal non-seminomatous germ cell tumor', 'cancer of the extragonadal non-seminomatous germ cell', 'malignant neoplasm of extragonadal non-seminomatous germ cell', 'extragonadal non-seminomatous germ cell cancer', 'malignant tumour of the extragonadal non-seminomatous germ cell', 'malignant tumor of the extragonadal non-seminomatous germ cell', 'malignant extragonadal non-seminomatous germ cell tumour', 'cancer of extragonadal non-seminomatous germ cell', 'extragonadal primary Nonseminoma', 'malignant extragonadal Nonseminoma', 'malignant tumour of extragonadal non-seminomatous germ cell', 'primary malignant extragonadal Nonseminoma', 'malignant extragonadal non-seminomatous germ cell neoplasm']",5677,,,C1334582,,C8885,,,,,,
mondo:0003579,retinal nerve fiber layer disorder,"['retinal nerve fiber bundle defects', 'nerve fiber bundle defect', 'nerve fiber layer of retina disease or disorder', 'disorder of nerve fiber layer of retina', 'disorder of nerve fibre layer of retina', 'retinal nerve fibre bundle deficiency', 'disease of nerve fibre layer of retina', 'nerve fiber layer of retina disease', 'nerve fibre layer of retina disease', 'nerve fibre layer of retina disease or disorder', 'retinal nerve fiber bundle deficiency', 'retinal nerve fibre bundle defects', 'nerve fibre bundle defect', 'disease of nerve fiber layer of retina', 'disease or disorder of nerve fibre layer of retina']",5678,,,C3665426,,,,,362.85,,,
mondo:0003581,ovarian embryonal carcinoma,"['ovarian embryonal carcinoma', 'ovary embryonal carcinoma', 'embryonal carcinoma', 'embryonal carcinoma of the ovary', 'embryonal carcinoma of ovary']",5681,,,C0346183,,C8108,1000415,,,,,
mondo:0003582,hereditary breast ovarian cancer syndrome,"['BRCA1- and BRCA2-associated hereditary breast and ovarian cancer', 'familial breast/ovarian cancer (BRCA1, BRCA2)', 'hereditary breast and ovarian cancer', 'familial breast and ovarian cancer syndrome', 'hereditary breast/ovarian cancer (BRCA1, BRCA2)', 'HBOC syndrome', 'hereditary breast ovarian cancer', 'BRCA1- and BRCA2-associated hereditary breast and ovarian cancer (HBOC)', 'syndrome, HBOC', 'hereditary breast and ovarian cancer syndrome', 'syndromes, HBOC', 'HBOC syndromes']",5683,,145,C0677776,"['0.2942', '-0.01854', '-0.233', '0.5156', '0.8174', '-0.785', '0.5117', '0.7026', '-0.00835', '-0.1184', '0.7876', '0.2174', '-0.4863', '0.624', '-0.3633', '-0.3406', '-0.427', '-0.599', '-0.853', '-0.5044', '-0.2734', '-0.7744', '-0.4707', '-0.2218', '0.4238', '-0.5425', '0.4175', '0.2129', '0.5713', '0.05505', '0.7524', '-0.4944', '0.3179', '-0.7817', '0.8003', '-0.2207', '-0.947', '0.2109', '-0.2544', '-0.1492', '0.3855', '-0.1573', '0.2722', '-0.198', '0.209', '-0.2041', '-0.2742', '-1.017', '1.385', '-0.005432', '-0.091', '-0.4624', '0.203', '-0.1929', '-0.5703', '0.2471', '-0.1626', '0.1765', '-0.969', '-1.003', '0.562', '-0.0417', '-0.1131', '-0.4639', '-0.39', '0.6', '0.4307', '0.1764', '0.12317', '0.895', '-0.00824', '0.8013', '-0.03183', '-0.3196', '1.411', '0.6196', '0.076', '-0.03976', '-0.1101', '0.4082', '-0.2', '0.2417', '-0.05792', '-0.1927', '-0.1365', '0.126', '0.999', '0.3823', '0.561', '-0.3047', '0.0464', '0.03433', '-0.2942', '0.3655', '-0.01501', '0.3489', '-0.2438', '-0.6216', '-0.6143', '-0.2499']",C8493,,D061325,,C50,,
mondo:0003584,visual cortex disorder,"['disorder of visual cortex', 'visual cortex dysfunction', 'visual cortex disease or disorder', 'visual cortex disease', 'disease of visual cortex']",5691,,,C0234398,,C35275,,,377.7,H47.6,,
mondo:0003585,adult liposarcoma,"['liposarcoma of adults', 'adult liposarcoma', 'liposarcoma']",5693,,,C0278608,,C7811,,,,,,
mondo:0003586,esophagus liposarcoma,"['liposarcoma of the esophagus', 'esophagus liposarcoma', 'liposarcoma of the oesophagus', 'liposarcoma of esophagus', 'liposarcoma of oesophagus', 'esophageal liposarcoma']",5694,,,C1333456,,C5705,,,,,,
mondo:0003587,pediatric liposarcoma,"['childhood liposarcoma', 'pediatric liposarcoma', 'liposarcoma']",5695,,,C0279984,,C8091,,,,,,
mondo:0003588,larynx liposarcoma,"['laryngeal liposarcoma', 'lip larynx sarcoma', 'liposarcoma of larynx', 'liposarcoma of the larynx', 'larynx liposarcoma']",5696,,,C1334372,,C6021,,,,,,
mondo:0003589,liposarcoma of the ovary,"['liposarcoma of ovary', 'ovarian liposarcoma', 'ovary liposarcoma']",5697,,,C1335165,,C6419,,,,,,
mondo:0003590,fibroblastic liposarcoma,"['fibroblastic liposarcoma', 'fibroblastic liposarcoma (morphologic abnormality)']",5698,,,C1266130,,C6509,,,,,,
mondo:0003591,kidney liposarcoma,"['kidney liposarcoma', 'liposarcoma of the kidney', 'liposarcoma of kidney', 'renal liposarcoma']",5699,,,C1335745,,C6185,,,,,,
mondo:0003592,gastric liposarcoma,"['liposarcoma of the stomach', 'gastric liposarcoma', 'stomach liposarcoma', 'liposarcoma of stomach']",5700,,,C1333778,,C5488,,,,,,
mondo:0003593,breast liposarcoma,"['liposarcoma of breast', 'breast liposarcoma', 'liposarcoma of the breast']",5701,,,C1332632,,C5187,,,,,,
mondo:0003594,mixed liposarcoma,"['mixed liposarcoma', 'mixed liposarcoma (morphologic abnormality)']",5703,,,C0334472,,C4253,,,,,,
mondo:0003595,sclerosing liposarcoma,,5704,,,C0334469,,C6507,,,171.9,,,
mondo:0003596,spindle cell liposarcoma,['spindle cell liposarcoma'],5705,,,C1275275,,C27489,,,171.9,,,
mondo:0003598,median nerve neuropathy,"['median nerve peripheral neuropathy', 'peripheral neuropathy of median nerve']",571,,,,,,,D020423,354.1,,,
mondo:0003599,vulvar liposarcoma,"['mammalian vulva liposarcoma', 'vulvar liposarcoma', 'liposarcoma of mammalian vulva']",5711,,,C2184082,,C40321,,,,,,
mondo:0003600,cutaneous liposarcoma,"['liposarcoma of zone of skin', 'cutaneous liposarcoma', 'liposarcoma of the skin', 'liposarcoma of skin', 'skin liposarcoma', 'zone of skin liposarcoma']",5712,,,C1333175,,C5615,,,,,,
mondo:0003601,mediastinum liposarcoma,"['liposarcoma of mediastinum', 'mediastinum liposarcoma', 'lip mediastinum sarcoma', 'mediastinal liposarcoma', 'liposarcoma of the mediastinum']",5713,,,C1334663,,C6614,,,,,,
mondo:0003602,intracranial liposarcoma,,5714,,,C1334242,,C6973,,,,,,
mondo:0003603,non-functioning pituitary gland neoplasm,"['non-functioning pituitary tumor', 'non-functioning neoplasm of pituitary', 'non-functioning neoplasm of the pituitary', 'nonfunctional pituitary gland neoplasm', 'non-functioning pituitary neoplasm', 'non-functioning tumor of the pituitary', 'non-functioning tumour of pituitary gland', 'non-functioning tumor of pituitary', 'non-functioning pituitary tumour', 'pituitary gland non-functioning endocrine neoplasm', 'non-functioning endocrine neoplasm of pituitary gland', 'non-functioning tumour of the pituitary', 'non-functioning pituitary gland tumor', 'non-functioning pituitary gland tumour', 'non-functioning tumour of pituitary', 'non-functioning pituitary gland neoplasm', 'non-functioning neoplasm of pituitary gland', 'Nonfunctioning pituitary tumour', 'non-functioning tumour of the pituitary gland', 'non-functioning tumor of pituitary gland', 'Nonfunctioning pituitary tumor', 'non-functioning tumor of the pituitary gland', 'non-functioning neoplasm of the pituitary gland']",,,,,,C4009,,,,,,
mondo:0003604,functioning pituitary gland neoplasm,"['pituitary gland functioning endocrine neoplasm', 'functioning endocrine neoplasm of pituitary gland', 'pituitary tumors, hormone producing', 'secretory pituitary tumour', 'pituitary neoplasms, hormone producing', 'growth hormone producing pituitary tumour', 'functioning pituitary gland neoplasm', 'somatotropinoma', 'hormone producing pituitary cancer', 'hormone producing pituitary neoplasm', 'functioning pituitary tumour']",5716,,,C3163678,,C7047,,,237.0,,,
mondo:0003606,adrenal medulla cancer,"['malignant tumour of adrenal medulla', 'malignant tumour of the adrenal medulla', 'malignant adrenal medulla neoplasm', 'malignant adrenal medulla tumour', 'malignant neoplasm of the adrenal medulla', 'malignant neoplasm of adrenal medulla', 'adrenal medulla neoplasm', 'adrenal medulla tumor', 'cancer of adrenal medulla', 'malignant adrenal medulla tumor', 'malignant tumor of adrenal medulla', 'malignant tumor of the adrenal medulla', 'adrenal medulla cancer', 'adrenal medulla tumour']",5719,,,C0344456,,C4396,,,,,,
mondo:0003607,neuritis of upper limb,['forelimb neuritis'],572,,,,,,,,354,,,
mondo:0003608,optic atrophy,"['atrophy of optic disc', 'atrophy of optic disk']",5723,,,C1744705,,C34863,,D009896,377.10,H47.2,,
mondo:0003609,seminal vesicle cystadenoma,['seminal vesicle cystadenoma'],5724,,,C1519234,,C39907,,,,,,
mondo:0003610,rete ovarii cystadenoma,['rete ovarii cystadenoma'],5725,,,C1514907,,C40019,,,,,,
mondo:0003611,uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease,"['uterine ligament papillary cystadenoma', 'uterine ligament papillary cystadenoma associated with von Hippel-Lindau disease']",5726,,,C3642324,,C40142,,,,,,
mondo:0003612,uterine ligament cancer,"['malignant neoplasm of uterine ligament', 'cancer of uterine ligament', 'tumour of the uterine ligament', 'uterine ligament cancer', 'malignant uterine ligament neoplasm']",5727,,,C0864950,,C126498,,,,,,
mondo:0003614,intravenous leiomyomatosis,['intravenous leiomyomatosis'],5729,,,C0346200,,C4518,,,238.1,,,
mondo:0003615,nerve compression syndrome,"['peripheral nerve entrapment syndrome', 'entrapment neuropathy', 'compression neuropathy']",573,,,,,C27221,,D009408,,,,
mondo:0003616,salpingitis isthmica nodosa,,5730,,,C0269043,,C40119,,,,,,
mondo:0003617,chronic salpingitis,"['salpingitis, chronic']",5731,,,C0269041,,C40118,,,,N70.11,,
mondo:0003618,pyosalpinx,['pyosalpingitis'],5732,,,C0034220,,C34968,,,,,,
mondo:0003619,salpingitis,['fallopian tube inflammation'],5733,,,C0036130,,C26880,,D012488,,,,
mondo:0003620,peripheral nervous system disorder,"['peripheral nervous system disease', 'nerve diseases, peripheral', 'peripheral nervous system disease or disorder', 'peripheral neuropathy', 'neuropathy, peripheral', 'PNS diseases', 'peripheral nervous system disorders', 'nerve disease, peripheral', 'PNS (peripheral nervous system) diseases', 'disease of peripheral nervous system', 'peripheral Neuropathies', 'peripheral nerve disease', 'peripheral nerve diseases', 'peripheral nervous system disorder', 'PNS disease', 'disorder of peripheral nervous system']",574,,,,,C27580,,D010523,356.9,,,
mondo:0003621,small intestinal vasoactive intestinal peptide producing tumor,"['small intestinal VIP producing tumor', 'small intestinal VIP producing tumour', 'small intestinal VIP-producing neuroendocrine tumor', 'small intestinal VIP-producing neuroendocrine tumour', 'small intestinal VIP-producing NET', 'small intestinal VIPoma', 'small intestinal vasoactive intestinal peptide producing tumor']",5740,,,C1336009,,C27455,,,,,,
mondo:0003622,pancreatic vasoactive intestinal peptide producing tumor,"['pancreatic VIP producing NET', 'pancreatic vasoactive intestinal peptide producing neoplasm', 'pancreatic VIP-producing neuroendocrine tumor', 'pancreatic vasoactive intestinal peptide producing tumor', 'pancreatic VIP producing tumour', 'pancreatic VIP producing tumor', 'pancreatic VIP producing neoplasm', 'pancreatic VIP-producing neuroendocrine tumour']",5741,,,C2033037,,C27454,,,,,,
mondo:0003624,acinic cell breast carcinoma,"['breast carcinoma of acinar cell', 'acinic cell breast carcinoma', 'acinar cell breast carcinoma']",5743,,,C1515868,,C40367,,,,,,
mondo:0003626,uterine ligament serous adenocarcinoma,['uterine ligament serous adenocarcinoma'],5747,,,C1519872,,C40136,,,,,,
mondo:0003627,rheumatic pulmonary valve disease,"['rheumatologic disorder of pulmonary valve', 'pulmonary valve rheumatologic disorder', 'rheumatic disease of pulmonary valve', 'rheumatic pulmonary incompetence']",5748,,,C0155579,,,,,397.1,,,
mondo:0003628,pulmonary valve disorder,"['pulmonary valve disorder', 'pulmonary valve disease', 'pulmonary valve disease or disorder', 'disease of pulmonary valve', 'disorder of pulmonary valve']",5749,,,C0034087,,C78579,,,424.3,,,
mondo:0003629,uterine corpus serous adenocarcinoma,"['uterine papillary serous carcinoma', 'body of uterus serous adenocarcinoma', 'uterine serous carcinoma/uterine papillary serous carcinoma']",5750,,,C1336921,,C27838,,,,,,
mondo:0003630,pancreatic serous cystadenocarcinoma,"['pancreatic serous cystadenocarcinoma', 'serous cystadenocarcinoma of the pancreas', 'serous cystadenocarcinoma of pancreas', 'pancreas serous adenocarcinoma']",5751,,424073,C1335315,,C5724,,,,,,
mondo:0003631,cervical serous adenocarcinoma,['cervical serous adenocarcinoma'],5752,,,C1516431,,C40201,,,,,,
mondo:0003632,endocervicitis,['endocervix inflammation'],5757,,,C0014127,,C26762,,,,,,
mondo:0003633,malignant mesenchymoma,"['mesenchymoma, malignant (morphologic abnormality)', 'mesenchymoma, malignant']",5758,,,,,C4268,,,,,,
mondo:0003634,proteinuria,,576,,,,,,,D011507,791.0,R80,,
mondo:0003635,sebaceous breast carcinoma,"['breast sebaceous adenocarcinoma', 'sebaceous breast carcinoma', 'sebaceous adenocarcinoma of breast']",5760,,,C1519207,,C40369,,,,,,
mondo:0003636,vulvar sebaceous carcinoma,"['mammalian vulva sebaceous adenocarcinoma', 'sebaceous adenocarcinoma of mammalian vulva']",5761,,,C1520094,,C40309,,,,,,
mondo:0003637,clear cell-sugar-tumor of the lung,"['lung clear cell tumor', 'lung clear cell tumour', 'clear cell-Sugar-tumor of the lung', 'lung clear cell-sugar-tumor', 'Sugar tumour', 'Sugar tumor', 'CCSTL', 'clear cell-Sugar-tumor of lung']",5763,,,C1333065,,C38152,,,,,,
mondo:0003638,lung meningioma,"['meningioma of the lung', 'meningioma of lung', 'lung meningioma', 'primary pulmonary meningioma', 'lung primary meningioma', 'pulmonary meningioma', 'lung meningioma (disease)']",5764,,,C1334450,,C5668,,,,,,
mondo:0003639,lung hilum neoplasm,"['tumor of lung hilus', 'tumour of lung hilus', 'hilar lung tumor', 'hilar lung neoplasm', 'neoplasm of hilus of lung', 'lung hilum tumour', 'lung hilus tumor', 'lung hilus tumour', 'lung hilum tumor', 'lung hilus neoplasm (disease)', 'neoplasm of lung hilus', 'hilar lung tumour', 'lung hilum neoplasm']",5767,,,C1290358,,C5671,,,,,,
mondo:0003640,verruciform xanthoma of skin,"['skin verruciform xanthoma', 'verruciform xanthoma of the skin', 'verruciform xanthoma (morphologic abnormality)', 'cutaneous verruciform xanthoma', 'verruciform xanthoma']",5769,,,C0346054,,C4478,,,215.9,,,
mondo:0003641,central nervous system hematopoietic neoplasm,"['hematopoietic neoplasm of central nervous system', 'central nervous system haematopoietic neoplasms', 'hematopoietic tumor of central nervous system', 'haematopoietic neoplasm of the CNS', 'haematopoietic tumour of central nervous system', 'haematopoietic neoplasm of the central nervous system', 'hematopoietic tumor of the central nervous system', 'lymphomas and hemopoietic neoplasms of CNS', 'CNS hematopoietic neoplasm', 'central nervous system hematopoietic neoplasm', 'lymphomas and hemopoietic neoplasms of the CNS', 'haematopoietic neoplasm of CNS', 'hematopoietic neoplasm of the central nervous system', 'haematopoietic neoplasm of central nervous system', 'CNS hematopoietic tumor', 'CNS haematopoietic neoplasm', 'hematopoietic and lymphoid system neoplasm of central nervous system', 'hematopoietic neoplasm of the CNS', 'CNS haematopoietic tumour', 'central nervous system hematopoietic neoplasms', 'haematopoietic tumour of the central nervous system', 'central nervous system haematopoietic and lymphoid system neoplasm', 'central nervous system hematopoietic and lymphoid system neoplasm', 'central nervous system haematopoietic tumour', 'central nervous system hematopoietic tumor', 'hematopoietic neoplasm of CNS', 'central nervous system hematologic cancer', 'haematopoietic and lymphoid system neoplasm of central nervous system']",5772,,,C1332882,,C5503,,,,,,
mondo:0003643,giant hemangioma,['giant hemangioma'],5774,,,C1333817,,C27777,,,,,,
mondo:0003644,cavernous hemangioma of colon,"['cavernous angioma of the colon', 'cavernous hemangioma of the colon', 'colonic cavernous hemangioma', 'colonic cavernous angioma', 'cavernous angioma of colon', 'colon cavernous angioma', 'cavernous hemangioma of colon', 'colon cavernous hemangioma']",5775,,,C1333086,,C5395,,,,,,
mondo:0003645,cavernous hemangioma of face,"['cavernous hemangioma of the Face', 'face cavernous hemangioma', 'cavernous hemangioma of face']",5776,,,C1332863,,C7053,1000152,,,,,0007486
mondo:0003646,rectum neuroendocrine neoplasm,"['rectum neuroendocrine tumor, well differentiated, low or intermediate grade', 'rectal NET', 'rectum neuroendocrine neoplasm', 'neuroendocrine neoplasm of the rectum', 'rectal neuroendocrine neoplasm', 'NET of the rectum', 'neuroendocrine tumour of rectum', 'neuroendocrine neoplasm of rectum', 'rectum neuroendocrine tumor', 'rectum neuroendocrine tumour', 'rectum NET', 'neuroendocrine tumor of rectum']",5777,,100081,C1335686,,C5698,,,,,,
mondo:0003647,atrophic flaccid tympanic membrane,,5781,,,C0155470,,,,,384.81,,,
mondo:0003648,tympanic membrane disorder,"['tympanic membrane disease', 'tympanic membrane disease or disorder', 'disease of tympanic membrane', 'disorder of tympanic membrane']",5782,,,C0041825,,,,,384.9,,,
mondo:0003649,esophageal neuroendocrine tumor,"['esophageal neuroendocrine tumor', 'neuroendocrine tumour of oesophagus', 'esophagus neuroendocrine tumor', 'neuroendocrine neoplasm of oesophagus', 'esophagus NET', 'oesophagus neuroendocrine tumour', 'esophageal neuroendocrine neoplasm', 'esophageal well differentiated endocrine tumour', 'oesophagus neuroendocrine neoplasm', 'oesophagus NET', 'neuroendocrine tumor of esophagus', 'oesophagus neuroendocrine tumor, well differentiated, low or intermediate grade', 'esophagus neuroendocrine tumor, well differentiated, low or intermediate grade', 'esophageal well differentiated endocrine tumor', 'NEN of oesophagus', 'esophageal NEN', 'esophageal well differentiated endocrine tumor/carcinoma', 'esophagus neuroendocrine neoplasm', 'NEN of esophagus', 'esophageal NET', 'neuroendocrine neoplasm of esophagus']",5784,,506136,C2987260,,C95616,,,,,,
mondo:0003650,mixed hepatoblastoma,['mixed epithelial and mesenchymal hepatoblastoma'],5789,,,C1334784,,C7097,,,,,,
mondo:0003651,macrotrabecular hepatoblastoma,,5798,,,C1334543,,C7095,,,,,,
mondo:0003652,acute urate nephropathy,"['uric acid urolithiasis', 'uric acid nephrolithiasis']",580,,,C0403719,,C123037,,,583.9,,,
mondo:0003653,stork bite,"['Unna^s nevus', 'Salmon patch nevus']",5806,,,,,,,,,,,
mondo:0003654,childhood parosteal osteosarcoma,"['childhood parosteal osteogenic sarcoma', 'childhood parosteal osteosarcoma']",5809,,,C1332994,,C6589,,,,,,
mondo:0003655,cerebral lymphoma,"['brain primary lymphoma', 'primary lymphoma, brain', 'primary lymphoma of the cerebrum', 'primary lymphoma of cerebrum', 'primary cerebral lymphoma', 'cerebral lymphoma']",5815,,,C0240803,,C7611,,,,,,
mondo:0003656,hemoglobinuria,,582,,,C0019048,,,,D006456,791.2,R82.3,,
mondo:0003658,"B-cell lymphoma, unclassifiable, with features intermediate between diffuse large b-cell lymphoma and classical Hodgkin lymphoma","['B-cell lymphoma, unclassifiable, with features Intermediate between diffuse large B-cell lymphoma and Classic Hodgkin lymphoma', 'B-cell lymphoma, unclassifiable, with features Intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma', 'Grey zone lymphoma', 'Gray zone lymphoma', 'large B-cell lymphoma with Hodgkin features', 'Hodgkin-like anaplastic large cell lymphoma']",5822,,,C1333878,,C37869,,,,,,
mondo:0003659,pediatric lymphoma,"['childhood lymphoma', 'lymphoma', 'pediatric lymphoma']",5823,,,C1332979,,C5165,,,,,,
mondo:0003660,adult lymphoma,"['lymphoma', 'lymphoma of adults', 'adult lymphoma']",5825,,,C1332206,,C7587,,,,,,
mondo:0003661,breast lymphoma,"['lymphoma of breast', 'lymphoma of the breast', 'malignant lymphoma of breast', 'primary breast lymphoma', 'breast lymphoma']",5826,,,C1704251,,C4671,,,,,,
mondo:0003663,uterine ligament endometrioid adenocarcinoma,"['uterine ligament endometrioid adenocarcinoma', 'endometrioid adenocarcinoma of uterine ligament']",5829,,,C1519868,,C40138,,,,,,
mondo:0003664,hemolytic anemia,"['anemia hemolytic', 'anemia, hemolytic', 'anaemia hemolytic', 'hemolytic anemia']",583,,,,,C34376,0005558,D000743,,D55-D59,,
mondo:0003665,cervical endometrioid adenocarcinoma,"['endometrioid carcinoma of cervix', 'cervical endometrioid carcinoma', 'endometrioid carcinoma of the cervix', 'endometrioid adenocarcinoma of the cervix uteri', 'endometrioid carcinoma of uterine cervix', 'endometrioid carcinoma of the uterine cervix', 'endometrioid carcinoma of the cervix uteri', 'endometrioid adenocarcinoma of uterine cervix', 'endometrioid adenocarcinoma of cervix uteri', 'cervical endometrioid adenocarcinoma', 'cervix endometrioid adenocarcinoma', 'cervix uteri endometrioid carcinoma', 'uterine cervix endometrioid adenocarcinoma', 'endometrioid adenocarcinoma of cervix', 'endometrioid adenocarcinoma of the uterine cervix', 'cervix uteri endometrioid adenocarcinoma', 'cervix endometrioid carcinoma', 'endometrioid carcinoma of cervix uteri', 'endometrioid adenocarcinoma of the cervix', 'uterine cervix endometrioid carcinoma']",5830,,,C1332913,,C6343,1000164,,,,,
mondo:0003666,fallopian tube endometrioid adenocarcinoma,"['endometrioid carcinoma of fallopian tube', 'endometrioid carcinoma of the fallopian tube', 'endometrioid adenocarcinoma of fallopian tube', 'fallopian tube endometrioid carcinoma', 'fallopian tube endometrioid adenocarcinoma', 'fallopian tube endometrioid neoplasm', 'endometrioid adenocarcinoma of the fallopian tube', 'fallopian tube endometrioid cancer']",5831,,,C1517113,,C6279,,,,,,
mondo:0003668,extragonadal seminoma,"['primary extragonadal seminoma', 'extragonadal primary seminoma', 'extragonadal seminoma']",5838,,,C1333502,,C7327,,,,,,
mondo:0003669,testicular seminoma,"['seminomatous germ cell tumour of testis', 'testicular seminoma', 'seminoma of the testis', 'seminoma testis', 'testicular seminoma Pure', 'testis seminoma', 'seminoma of testis', 'testicular seminomatous germ cell tumor', 'testicular seminomatous germ cell tumour', 'testicular seminoma (disease)', 'seminomatous germ cell tumor of testis']",5842,,842,,,C7328,0003101,,186.9,,,0100617
mondo:0003670,posteroinferior myocardial infarction,"['posteroinferior myocardial infarction by ECG finding', 'posteroinferior myocardial infarction by EKG finding']",5843,,,,,,,,,,,
mondo:0003671,septal myocardial infarction,['cardiac septum myocardial infarction (disease)'],5846,,,,,,,,,,,
mondo:0003672,posterior myocardial infarction,,5847,,,C0264706,,,,,,,,
mondo:0003673,apical myocardial infarction,,5848,,,,,,,,,,,
mondo:0003674,subendocardial myocardial infarction,['subendocardium layer myocardial infarction (disease)'],5849,,,C0262568,,,,,,,,
mondo:0003675,posterolateral myocardial infarction,,5851,,,,,,,,,,,
mondo:0003676,inferolateral myocardial infarct,,5852,,,,,,,,,,,
mondo:0003677,lateral myocardial infarction,,5853,,,,,,,,,,,
mondo:0003678,silent myocardial infarction,['silent myocardial infarction'],5854,,,C0340324,,C35400,,,,,,
mondo:0003679,anteroseptal myocardial infarction,,5855,,,C0262565,,,,D056988,,,,
mondo:0003680,periosteal chondrosarcoma,"['juxtacortical chondrosarcoma', 'periosteum chondrosarcoma (disease)', 'juxtacortical chondrosarcoma (morphologic abnormality)', 'periosteal chondrosarcoma']",5866,,,C0334549,,C7357,,,,,,
mondo:0003681,myxoid chondrosarcoma,"['MYCHS', 'myxoid chondrosarcoma']",5861,,,C0334551,,C4303,,,,,,
mondo:0003682,localized chondrosarcoma,"['chondrosarcoma, localised', 'chondrosarcoma, localized', 'localized chondrosarcoma']",5862,,,C0855011,,C8778,,,,,,
mondo:0003684,clear cell chondrosarcoma,"['clear cell chondrosarcoma (morphologic abnormality)', 'clear cell chondrosarcoma']",5867,,,C1266167,,C6475,,,,,,
mondo:0003685,retroperitoneal germ cell neoplasm,"['germ cell tumour of retroperitoneum', 'germ cell neoplasm of the retroperitoneum', 'germ cell tumour of the retroperitoneum', 'germ cell tumor of retroperitoneum', 'germ cell neoplasm of retroperitoneum', 'retroperitoneal germ cell tumor', 'germ cell tumor of the retroperitoneum', 'retroperitoneal germ cell tumour']",5874,,,C1335776,,C6447,,,,,,
mondo:0003686,apocrine sweat gland neoplasm,"['tumour of apocrine sweat gland', 'apocrine sweat gland tumor', 'tumor of apocrine sweat gland', 'apocrine tumour', 'apocrine skin neoplasm', 'apocrine skin tumor', 'apocrine neoplasm of the skin', 'neoplasm of apocrine sweat gland', 'apocrine skin tumour', 'apocrine sweat gland neoplasm (disease)', 'apocrine tumour of skin', 'apocrine sweat gland tumour', 'apocrine tumour of the skin', 'apocrine tumor', 'apocrine tumor of skin', 'apocrine neoplasm of skin', 'apocrine neoplasm', 'apocrine tumor of the skin']",5876,,,C1332318,,C6798,,,,,,
mondo:0003687,endocardium cancer,"['malignant tumor of endocardium', 'cancer of endocardium', 'malignant endocardium neoplasm', 'malignant tumour of the endocardium', 'malignant endocardial tumor', 'malignant neoplasm of endocardium', 'malignant tumour of endocardium', 'malignant neoplasm of the endocardium', 'malignant tumor of the endocardium', 'malignant endocardial tumour', 'endocardium cancer', 'malignant endocardial neoplasm']",5877,,,C0346612,,C4570,,,,,,
mondo:0003688,well differentiated papillary mesothelioma,"['well-differentiated mesothelial papillary tumour', 'well-differentiated papillary tumour of the mesothelium', 'benign/Intermediate mesothelioma', 'well-differentiated mesothelial papillary tumor', 'benign intermediate mesothelioma', 'well differentiated papillary mesothelioma', 'well-differentiated mesothelial papillary neoplasm', 'well-differentiated papillary neoplasm of mesothelium', 'WDPM', 'well-differentiated papillary tumor of mesothelium', 'well-differentiated papillary tumor of the mesothelium', 'well-differentiated papillary neoplasm of the mesothelium', 'well-differentiated papillary tumour of mesothelium']",5884,,,C1337012,,C7635,,,,,,
mondo:0003689,familial hemolytic anemia,"['congenital hemolytic anaemia', 'anemia hemolytic congenital', 'congenital hemolytic anemia', 'hereditary hemolytic anaemia', 'anaemia hemolytic congenital', 'hereditary hemolytic anemia']",589,,,,,C34379,,D000745,282.9,,,
mondo:0003690,adult anaplastic ependymoma,"['anaplastic ependymoma of adults', 'adult anaplastic ependymoma', 'anaplastic ependymoma', 'adult malignant ependymoma', 'malignant adult ependymoma']",5890,,,C0280787,,C8269,,,,,,
mondo:0003691,childhood malignant mesenchymoma,"['malignant mesenchymoma', 'pediatric malignant mesenchymoma', 'childhood malignant mesenchymoma', 'malignant mesenchymoma of childhood', 'paediatric malignant mesenchymoma']",5893,,,C0279991,,C8097,,,,,,
mondo:0003692,adult malignant mesenchymoma,"['adult malignant mesenchymoma', 'malignant mesenchymoma', 'malignant mesenchymoma of adults']",5894,,,C0279548,,C7947,,,,,,
mondo:0003693,clear cell cystadenofibroma,['clear cell cystadenofibroma'],5895,,,C1377853,,C8988,,,,,,
mondo:0003694,ovarian clear cell cystadenofibroma,"['ovarian clear cell cystadenofibroma', 'clear cell cystadenofibroma of ovary', 'ovary clear cell cystadenofibroma']",5896,,,C1518695,,C40086,,,,,,
mondo:0003695,ovarian clear cell adenofibroma,"['ovary clear cell adenofibroma', 'clear cell adenofibroma of ovary', 'ovarian clear cell adenofibroma']",5897,,,C1518694,,C40085,,,,,,
mondo:0003697,non-invasive verrucous carcinoma of the penis,"['penis non-invasive verrucous carcinoma', 'non-invasive penile verrucous carcinoma', 'non-invasive verrucous carcinoma of the penis', 'non-invasive verrucous carcinoma of penis']",5907,,,C1334984,,C27791,,,,,,
mondo:0003698,penis verrucous carcinoma,"['verrucous squamous carcinoma of the penis', 'squamous carcinoma of penis, verrucous type', 'penis verrucous carcinoma', 'verrucous carcinoma of the penis', 'verrucous penile carcinoma', 'verrucous penile squamous cell carcinoma', 'verrucous squamous carcinoma of penis', 'squamous carcinoma of the penis, verrucous type', 'verrucous carcinoma of penis', 'verrucous penile squamous carcinoma']",5908,,,C1336955,,C6982,,,,,,
mondo:0003699,phobic disorder,['phobia'],591,,,,,C35420,1001908,D010698,300.20,,,
mondo:0003700,brachial plexus neoplasm,"['tumor of the brachial plexus', 'neoplasm of brachial plexus', 'brachial nerve plexus neoplasm (disease)', 'tumour of brachial plexus', 'tumor of brachial plexus', 'brachial nerve plexus tumour', 'brachial plexus tumor', 'brachial plexus neoplasms', 'tumour of brachial nerve plexus', 'brachial nerve plexus tumor', 'neoplasm of the brachial plexus', 'tumor of brachial nerve plexus', 'brachial plexus neoplasm', 'brachial plexus tumour', 'neoplasm of brachial nerve plexus', 'tumour of the brachial plexus']",5913,,,C1332602,,C5823,,,,,,
mondo:0003701,thyroid gland diffuse sclerosing papillary carcinoma,"['papillary carcinoma, diffuse sclerosing', 'nonencapsulated sclerosing carcinoma', 'nonencapsulated sclerosing adenocarcinoma', 'nonencapsulated sclerosing tumor', 'nonencapsulated sclerosing tumour', 'thyroid gland diffuse sclerosing papillary carcinoma', 'nonencapsulated sclerosing neoplasm', 'nonencapsulated sclerosing papillary thyroid carcinoma']",5914,,,C1321862,,C7427,,,,,,
mondo:0003702,uterus intravascular leiomyomatosis,"['intravenous leiomyomatosis of the uterus', 'intravascular leiomyomatosis of the uterus', 'uterine corpus intravenous leiomyomatosis', 'intravenous leiomyomatosis of uterus', 'intravascular leiomyomatosis of uterus', 'uterus intravenous leiomyomatosis']",5915,,,,,C5356,,,,,,
mondo:0003704,uterine corpus diffuse leiomyomatosis,"['uterine corpus leiomyomatosis', 'leiomyomatosis of body of uterus', 'uterine corpus diffuse leiomyomatosis', 'body of uterus leiomyomatosis']",5917,,,C1519855,,C40170,,,,,,
mondo:0003705,adult brainstem mixed glioma,"['adult brain stem mixed glioma', 'adult brainstem mixed glioma']",5921,,,C1377915,,C9371,,,,,,
mondo:0003706,adult brainstem astrocytoma,"['adult brain stem astrocytoma', 'adult brainstem astrocytoma']",5922,,,C1332191,,C6954,,,,,,
mondo:0003707,distal biliary tract carcinoma,"['extrahepatic (distal) bile duct cancer', 'carcinoma of distal biliary tract', 'carcinoma of the distal biliary tract', 'distal biliary tract carcinoma', 'distal bile duct cancer', 'distal bile duct carcinoma']",5923,,,C1333308,,C7109,,,,,,
mondo:0003708,extrahepatic bile duct small cell adenocarcinoma,"['extrahepatic bile duct small cell neuroendocrine carcinoma', 'Oat cell extrahepatic bile duct carcinoma', 'extrahepatic bile duct small cell NEC', 'small cell adenocarcinoma of the extrahepatic bile duct', 'Oat cell carcinoma of extrahepatic bile duct', 'small cell adenocarcinoma of extrahepatic bile duct', 'small cell extrahepatic bile duct carcinoma', 'small cell extrahepatic bile duct neuroendocrine carcinoma', 'Oat cell carcinoma of the extrahepatic bile duct']",5926,,,C1335979,,C5845,,,,,,
mondo:0003709,agoraphobia,"['fear of open spaces', 'fear of open spaces (finding)']",593,,,,,C34362,1001872,D000379,,F40.0,,
mondo:0003710,ovarian mixed germ cell neoplasm,"['ovary mixed germ cell tumor', 'mixed germ cell tumor of the ovary', 'mixed germ cell neoplasm of the ovary', 'ovarian mixed germ cell tumor', 'ovarian mixed germ cell tumour', 'mixed germ cell tumour of ovary', 'mixed germ cell tumor of ovary', 'mixed germ cell tumour', 'ovarian mixed germ cell neoplasm', 'mixed germ cell tumour of the ovary', 'mixed germ cell tumor', 'mixed germ cell neoplasm of ovary', 'ovary mixed germ cell tumour']",5936,,,C0280135,,C8114,,,,,,
mondo:0003712,angiokeratoma of mibelli,,5948,,,C0263640,,C3927,,,,,,
mondo:0003713,angiokeratoma circumscriptum,,5949,,,C0263638,,C7751,,,,,,
mondo:0003714,bladder urachal squamous cell carcinoma,['bladder urachal squamous cell carcinoma'],5957,,,C1511206,,C39845,,,,,,
mondo:0003715,bladder urachal carcinoma,"['urachal carcinoma', 'bladder urachal carcinoma', 'bladder urachal cancer']",5958,,,C1511205,,C39842,,C536475,,,,
mondo:0003716,renal pelvis papillary urothelial carcinoma,"['renal pelvis papillary urothelial carcinoma', 'papillary carcinoma of kidney pelvis', 'renal pelvis papillary carcinoma', 'kidney pelvis papillary carcinoma', 'papillary carcinoma of renal pelvis', 'papillary carcinoma of the kidney pelvis', 'papillary carcinoma of the renal pelvis']",5973,,,C1377909,,C6148,,,,,,
mondo:0003717,renal pelvis papillary tumor,"['papillary tumor of renal pelvis', 'papillary neoplasm of renal pelvis', 'papillary tumour of renal pelvis', 'papillary tumor of the renal pelvis', 'renal pelvis papillary tumor', 'papillary neoplasm of the renal pelvis', 'renal pelvis papillary urothelial neoplasm', 'papillary tumour of the renal pelvis']",5975,,,C0853688,,C8603,,,,,,
mondo:0003718,occlusion precerebral artery,"['occlusion and stenosis of multiple and bilateral precerebral arteries', 'occlusion and stenosis of precerebral artery']",5976,,,C0265090,,,,,433.9,,,
mondo:0003719,renal pelvis neoplasm,"['tumor of the kidney pelvis', 'renal pelvis neoplasm', 'renal pelvis tumor', 'neoplasm of the kidney pelvis', 'kidney pelvis tumor', 'tumor of the renal pelvis', 'tumor of kidney pelvis', 'tumour of the kidney pelvis', 'tumor of renal pelvis', 'renal pelvis tumour', 'tumour of the renal pelvis', 'kidney pelvis tumour', 'kidney pelvis neoplasm', 'neoplasm of renal pelvis', 'tumour of renal pelvis', 'tumour of kidney pelvis', 'renal pelvis neoplasm (disease)', 'neoplasm of the renal pelvis', 'neoplasm of kidney pelvis']",5977,,,C0346260,,C8404,,,239.5,,,
mondo:0003720,kidney fibrosarcoma,"['fibrosarcoma of kidney', 'kidney fibrosarcoma', 'fibrosarcoma of the kidney', 'kidney fibrosarcoma (disease)', 'renal fibrosarcoma']",5982,,,C0238208,,C7726,,,,,,
mondo:0003721,kidney osteogenic sarcoma,"['osteosarcoma of kidney', 'kidney osteosarcoma (disease)', 'kidney extraskeletal osteosarcoma', 'osteogenic sarcoma of the kidney', 'kidney osteosarcoma', 'renal osteosarcoma', 'renal extraskeletal osteosarcoma', 'kidney osteogenic sarcoma', 'osteogenic sarcoma of kidney', 'osteosarcoma of the kidney', 'renal osteogenic sarcoma']",5983,,,C1335747,,C6181,,,,,,
mondo:0003722,internal auditory canal meningioma,"['meningioma of the internal auditory canal', 'meningioma of internal auditory canal', 'internal acoustic meatus meningioma (disease)']",5990,,,C1334227,,C5307,,,,,,
mondo:0003723,blunt duct adenosis of breast,"['breast blunt duct adenosis', 'blunt duct adenosis of the breast']",5996,,,C1332573,,C6941,,,,,,
mondo:0003724,non-proliferative fibrocystic change of the breast,"['non-proliferative fibrocystic change of breast', 'breast fibrocystic change, non-proliferative type', 'non-proliferative fibrocystic change']",5997,,,C1332628,,C6943,,,,,,
mondo:0003725,breast adenosis,"['adenosis of breast', 'adenosis - breast', 'microglandular adenosis', 'breast adenosis', 'adenosis', 'adenosis of the breast']",5998,,,C0085750,,C3484,0006891,D005348,,,,
mondo:0003726,apocrine adenosis of breast,"['apocrine adenosis of the breast', 'apocrine adenosis of breast', 'breast apocrine adenosis']",5999,,,C1332314,,C5198,,,,,,
mondo:0003727,animal phobia,"['fear of animals (finding)', 'zoophobia', 'fear of animals', 'zoophobia (finding)']",600,,,,,C35273,1001876,,,,,
mondo:0003728,breast fibrosarcoma,"['breast fibrosarcoma', 'fibrosarcoma of the breast', 'fibrosarcoma of breast', 'breast fibrosarcoma (disease)']",6001,,,C1332630,,C5185,,,,,,
mondo:0003729,aleukemic leukemia cutis,"['leukemia subleukemic', 'leukaemia subleukemic', 'aleukemic leukemia cutis']",6003,,,C0887846,,C4983,,,,,,
mondo:0003730,aleukemic leukemia,"['subleukemic leukaemia', 'subleukemic leukemia', 'aleukemic myelosis', 'aleukemic leukemia']",6004,,,C0877858,,C4982,,,208.80,,,
mondo:0003731,adult central nervous system teratoma,"['Central nervous system teratoma', 'teratoma of adult central nervous system', 'teratoma of the adult CNS', 'adult CNS teratoma', 'central nervous system teratoma of adults', 'teratoma of the adult central nervous system', 'teratoma of adult CNS', 'adult central nervous system teratoma']",6015,,,C1370506,,C5794,,,,,,
mondo:0003732,adult central nervous system mature teratoma,"['central nervous system mature teratoma of adults', 'adult central nervous system mature teratoma']",6016,,,C1332194,,C27400,,,,,,
mondo:0003733,central nervous system mature teratoma,"['mature teratoma', 'central nervous system mature teratoma', 'mature teratoma of the central nervous system', 'mature teratoma of central nervous system', 'mature teratoma of CNS', 'mature teratoma of the CNS', 'CNS mature teratoma']",6017,,,C1332886,,C7013,,,,,,
mondo:0003734,adult central nervous system immature teratoma,['adult central nervous system immature teratoma'],6018,,,C1332193,,C27401,,,,,,
mondo:0003735,central nervous system immature teratoma,"['immature teratoma of the CNS', 'CNS immature teratoma', 'immature teratoma of CNS', 'immature teratoma', 'immature teratoma of central nervous system', 'central nervous system immature teratoma', 'immature teratoma of the central nervous system']",6019,,,C1332883,,C7014,,,,,,
mondo:0003736,cancerophobia,"['fear of getting cancer', 'Cancerphobia', 'cancer phobia', 'fear of getting cancer (finding)']",602,,,,,C35492,1001879,,,,,
mondo:0003737,malignant testicular Leydig cell tumor,"['testicular Leydig cell tumor, malignant']",6021,,,C1515288,,C39942,,,,,,
mondo:0003738,selective IgE deficiency disease,"['selective immunoglobulin E deficiency', 'selective IgE immunodeficiency']",6024,,,C0398694,,C27143,,,279.03,,,
mondo:0003739,selective immunoglobulin deficiency disease,['selective Immunoglobulin isotype deficiency'],6025,,,C1335942,,C27870,,,,,,
mondo:0003740,AIDS phobia,['AIDS phobia'],603,,,C0853870,,C35614,1001873,,,,,
mondo:0003741,juvenile type testicular granulosa cell tumor,"['juvenile granulosa cell tumor', 'juvenile granulosa cell tumor (morphologic abnormality)', 'juvenile type granulosa cell tumor', 'juvenile type granulosa cell neoplasm', 'juvenile type granulosa cell tumour', 'juvenile granulosa cell tumour', 'juvenile granulosa cell tumour (morphologic abnormality)']",6032,,,C1515285,,C39947,,,,,,
mondo:0003742,heart fibrosarcoma,"['Cardiac fibrosarcoma', 'fibrosarcoma of the heart', 'heart fibrosarcoma', 'fibrosarcoma of heart', 'heart fibrosarcoma (disease)', 'cardiac fibrosarcoma']",6033,,,C1332844,,C5361,,,,,,
mondo:0003743,heart malignant hemangiopericytoma,"['heart hemangiopericytoma', 'malignant hemangiopericytoma of the heart', 'malignant heart hemangiopericytoma', 'heart spindle cell tumour', 'heart spindle cell tumor', 'malignant Cardiac hemangiopericytoma', 'malignant hemangiopericytoma of heart']",6034,,,C1334567,,C5365,,,,,,
mondo:0003744,spindle cell intraocular melanoma,"['uveal spindle cell melanoma', 'spindle cell melanoma of the uvea', 'spindle cell melanoma of uvea', 'spindle cell uveal melanoma']",6037,,,C0279687,,C7986,,,,,,
mondo:0003745,choroid spindle cell melanoma,"['spindle cell melanoma of the choroid', 'optic choroid spindle cell melanoma', 'spindle cell melanoma of optic choroid', 'spindle cell melanoma of choroid']",6041,,,C1333027,,C6099,,,,,,
mondo:0003746,ciliary body spindle cell melanoma,"['ciliary body spindle cell melanoma', 'spindle cell melanoma of the ciliary body', 'spindle cell melanoma of ciliary body']",6043,,,C1333052,,C6117,,,,,,
mondo:0003747,telangiectatic glomangioma,['telangiectatic glomangioma'],6048,,,C1336699,,C5345,,,,,,
mondo:0003748,flying phobia,,605,,,,,C35413,1001889,,,,,
mondo:0003749,esophageal disorder,"['oesophagus disease', 'disorder of oesophagus', 'disorder of esophagus', 'esophagus disease or disorder', 'esophagus disease', 'esophageal disorder', 'esophageal ulcer', 'disease or disorder of oesophagus', 'oesophagus disease or disorder', 'disease of oesophagus', 'disease of esophagus']",6050,,,C0014852,,C3027,,D004935,530.9,,,
mondo:0003750,childhood central nervous system germ cell tumor,"['childhood germ cell tumor of CNS', 'childhood germ cell tumour of the central nervous system', 'central nervous system paediatric germ cell cancer', 'pediatric CNS germ cell neoplasm', 'paediatric germ cell neoplasm of the CNS', 'childhood germ cell tumor of the central nervous system', 'childhood germ cell tumor of the CNS', 'childhood germ cell tumour of central nervous system', 'childhood germ cell tumour of CNS', 'central nervous system germ cell tumor', 'pediatric germ cell tumor of CNS', 'paediatric germ cell tumour of CNS', 'pediatric germ cell neoplasm of central nervous system', 'childhood CNS germ cell tumor', 'childhood germ cell tumour of the CNS', 'pediatric germ cell tumor of the CNS', 'pediatric germ cell neoplasm of CNS', 'pediatric central nervous system germ cell neoplasm', 'childhood germ cell neoplasm of central nervous system', 'central nervous system pediatric germ cell cancer', 'paediatric CNS germ cell neoplasm', 'childhood CNS germ cell tumour', 'paediatric CNS germ cell tumour', 'paediatric germ cell neoplasm of central nervous system', 'paediatric germ cell tumour of central nervous system', 'childhood germ cell neoplasm of CNS', 'central nervous system childhood germ cell tumour', 'paediatric central nervous system germ cell tumour', 'childhood central nervous system germ cell neoplasm', 'paediatric germ cell tumour of the CNS', 'paediatric germ cell tumour of the central nervous system', 'central nervous system germ cell tumour', 'paediatric germ cell neoplasm of the central nervous system', 'pediatric germ cell tumor of the central nervous system', 'childhood germ cell tumor of central nervous system', 'paediatric central nervous system germ cell neoplasm', 'childhood germ cell neoplasm of the CNS', 'pediatric germ cell tumor of central nervous system', 'pediatric germ cell neoplasm of the CNS', 'pediatric germ cell neoplasm of the central nervous system', 'pediatric CNS germ cell tumor', 'paediatric germ cell neoplasm of CNS', 'central nervous system childhood germ cell tumor', 'pediatric central nervous system germ cell tumor', 'childhood germ cell neoplasm of the central nervous system', 'childhood CNS germ cell neoplasm', 'childhood central nervous system germ cell tumor']",6052,,,C0278754,,C6205,,,,,,
mondo:0003751,childhood germ cell tumor,"['paediatric germ cell cancer', 'germ cell tumor', 'pediatric germ cell neoplasm', 'pediatric germ cell tumor', 'childhood germ cell neoplasm', 'pediatric germ cell cancer', 'germ cell tumour', 'paediatric germ cell tumour', 'paediatric germ cell neoplasm', 'childhood germ cell tumor']",6053,,,C0279014,,C7928,,,,,,
mondo:0003752,frontal sinus Schneiderian papilloma,"['Schneiderian papilloma of the frontal sinus', 'frontal sinus Schneiderian papilloma', 'Schneiderian papilloma of frontal sinus']",6054,,,C1333645,,C6837,,,,,,
mondo:0003753,nasal vestibule squamous papilloma,"['nasal vestibule squamous papilloma', 'papilloma of nasal vestibule', 'squamous papilloma of nasal vestibule', 'papilloma of the nasal vestibule', 'nasal vestibule papilloma', 'squamous papilloma of the nasal vestibule']",6059,,,C0339826,,C4369,,,478.19,,,
mondo:0003754,Brown-Sequard syndrome,"['Brown-Squard syndrome', 'Hemiparaplegic syndrome', 'Hemispinal cord syndrome', 'Hemicord syndrome']",606,,,,,C84601,1001279,D018437,,G83.81,,
mondo:0003755,urinary tract non-invasive transitional cell neoplasm,"['non-invasive transitional cell neoplasm of the urinary tract', 'non-invasive urothelial neoplasm']",6065,,,C1518361,,C39854,,,,,,
mondo:0003756,ovarian mucinous neoplasm,"['mucinous tumor of the ovary', 'ovarian mucinous tumor', 'ovarian mucinous neoplasm', 'mucinous neoplasm of ovary', 'malignant ovarian mucinous neoplasm', 'mucinous tumour of the ovary', 'mucinous tumour of ovary', 'mucinous neoplasm of the ovary', 'ovarian mucinous tumour', 'mucinous tumor of ovary']",6067,,,C1335168,,C5242,,,,,,
mondo:0003757,paraplegia,"['paraplegia, lower', 'severe or complete loss of motor function in the lower extremities and lower portions of the trunk']",607,,,C0030486,,C50687,,D010264,344.1,,,
mondo:0003758,childhood testicular germ cell tumor,"['paediatric testicular germ cell tumour', 'paediatric testicular germ cell neoplasm', 'pediatric testicular germ cell tumor', 'childhood testicular germ cell neoplasm', 'testicular germ cell tumor', 'testicular germ cell tumour of childhood', 'testicular germ cell tumor of childhood', 'pediatric testicular germ cell neoplasm', 'childhood testicular germ cell tumor', 'testicular germ cell tumour']",6082,,,C0796663,,C6552,,,,,,
mondo:0003759,childhood ovarian yolk sac tumor,"['ovary childhood endodermal sinus tumor', 'paediatric ovarian yolk Sac neoplasm', 'paediatric ovarian yolk Sac tumour', 'pediatric ovarian yolk Sac tumor', 'childhood ovarian yolk sac tumor', 'childhood ovarian endodermal sinus tumour', 'pediatric ovarian endodermal sinus tumor', 'childhood ovarian yolk Sac neoplasm', 'paediatric ovarian endodermal sinus neoplasm', 'pediatric ovarian yolk Sac neoplasm', 'childhood ovarian endodermal sinus tumor', 'ovary childhood endodermal sinus tumour', 'pediatric ovarian endodermal sinus neoplasm', 'paediatric ovarian endodermal sinus tumour', 'childhood ovarian endodermal sinus neoplasm']",6083,,,C1332993,,C6551,,,,,,
mondo:0003760,pediatric ovarian germ cell tumor,"['ovarian germ cell tumour', 'childhood ovarian germ cell neoplasm', 'ovarian germ cell tumor', 'paediatric ovarian germ cell neoplasm', 'pediatric ovarian germ cell tumor', 'ovarian germ cell tumour of childhood', 'ovarian germ cell tumor of childhood', 'childhood ovarian germ cell tumour', 'childhood ovarian germ cell tumor', 'pediatric ovarian germ cell neoplasm']",6084,,,C0796664,,C8588,,,,,,
mondo:0003761,leptomeningeal melanoma,"['melanoma of the leptomeninges', 'leptomeningeal melanoma', 'meningeal melanoma', 'melanoma of leptomeninges', 'leptomeninx melanoma (disease)']",6085,,,C1334386,,C5317,,,,,,
mondo:0003762,malignant leptomeningeal tumor,"['malignant neoplasm of leptomeninx', 'malignant tumour of leptomeninges', 'malignant neoplasm of the leptomeninges', 'malignant neoplasm of leptomeninges', 'malignant leptomeningeal tumor', 'malignant tumor of leptomeninges', 'malignant leptomeninx neoplasm', 'malignant tumor of the leptomeninges', 'malignant leptomeningeal neoplasm', 'leptomeningeal cancer', 'leptomeninx cancer', 'malignant tumour of the leptomeninges', 'cancer of leptomeninx']",6086,,,C1334596,,C8506,,,,,,
mondo:0003763,acute stress disorder,"['acute stress reaction', 'traumatic stress disorder']",6088,,,,,C92621,0005223,D000068099,308.9,F43.0,,
mondo:0003764,pediatric leptomeningeal melanoma,"['pediatric meningeal melanoma', 'childhood leptomeningeal melanoma', 'childhood meningeal melanoma', 'paediatric meningeal melanoma']",6089,,,C1332976,,C5318,,,,,,
mondo:0003765,adult leptomeningeal melanoma,"['melanoma of the adult leptomeninges', 'adult leptomeningeal melanoma', 'adult meningeal melanoma', 'melanoma of adult leptomeninges']",6090,,,C1332204,,C5319,,,,,,
mondo:0003766,thalamic cancer,"['malignant thalamus tumor', 'malignant tumour of thalamus', 'malignant tumor of the thalamus', 'malignant tumor of thalamus', 'malignant thalamus tumour', 'malignant thalamus tumors', 'dorsal plus ventral thalamus cancer', 'malignant thalamus neoplasm', 'malignant dorsal plus ventral thalamus neoplasm', 'malignant tumour of the thalamus', 'thalamic neoplasm', 'malignant thalamic neoplasm', 'cancer of dorsal plus ventral thalamus', 'malignant thalamus neoplasms', 'malignant neoplasm of dorsal plus ventral thalamus', 'malignant thalamic neoplasms', 'malignant neoplasm of thalamus', 'malignant thalamus tumours', 'malignant thalamic tumours', 'malignant neoplasm of the thalamus', 'malignant thalamic tumor', 'malignant thalamic tumors', 'malignant thalamic tumour', 'tumor of thalamus', 'tumour of thalamus']",6098,,,C0346902,,C4576,,,,,,
mondo:0003767,mitral valve disorder,"['chronic rheumatic mitral valve', 'disorder of mitral valve', 'rheumatic mitral valve incompetence', 'mitral valve disease or disorder', 'mitral valve disorder', 'rheumatic disease of mitral valve', 'rheumatic mitral valve regurgitation', 'disease of mitral valve', 'mitral valve disease', 'rheumatic mitral valve changes', 'rheumatic mitral insufficiency', 'mitral RH valve dis.']",61,,,C2939153,,C78446,,,424.0,,,
mondo:0003768,signet ring cell variant cervical mucinous adenocarcinoma,"['signet ring mucinous carcinoma', 'cervical mucinous adenocarcinoma, signet Ring cell variant', 'cervical mucinous adenocarcinoma, signet Ring cell type']",6101,,,C1516424,,C40205,,,,,,
mondo:0003769,herpetic gastritis,['Herpesviridae caused viral gastritis'],6102,,,C1333996,,C27341,,,,,,
mondo:0003770,thoracic spinal canal and spinal cord meningioma,"['meningioma of thoracic spinal canal and spinal cord', 'meningioma of the thoracic spinal canal and spinal cord', 'thoracic intraspinal meningioma']",6103,,,C1336738,,C5297,,,,,,
mondo:0003771,jugular foramen meningioma,"['jugular foramen meningioma (disease)', 'meningioma of jugular Foramen', 'meningioma of the jugular Foramen']",6110,,,C1334298,,C5293,,,,,,
mondo:0003772,cerebral meningioma,"['meningioma of the cerebral hemispheres', 'meningioma of the cerebrum', 'cerebral hemispheric meningioma', 'meningioma of cerebral hemispheres', 'meningioma of cerebrum', 'telencephalon meningioma (disease)']",6112,,,C0542564,,C4807,,,,,,
mondo:0003773,intracerebral cystic meningioma,,6113,,,C1334236,,C5269,,,,,,
mondo:0003774,cerebral convexity meningioma,['cerebral hemispheric convexity meningioma'],6114,,,C0751303,,C4959,,,,,,
mondo:0003775,lateral ventricle meningioma,"['telencephalic ventricle meningioma (disease)', 'meningioma of lateral ventricle', 'meningioma of the lateral ventricle']",6115,,,C1334380,,C5302,,,,,,
mondo:0003776,renal pelvis inverted papilloma,"['inverted papilloma of renal pelvis', 'inverted papilloma of the renal pelvis', 'renal pelvis inverted papilloma', 'inverted papilloma of the kidney pelvis', 'inverted papilloma of kidney pelvis', 'kidney pelvis inverted papilloma']",6118,,,C1335751,,C6187,,,,,,
mondo:0003777,renal pelvis urothelial papilloma,['renal pelvis urothelial papilloma'],6119,,,C1514844,,C4528,,,,,,
mondo:0003778,inborn error of immunity,"['immunodeficiency syndrome', 'deficiency syndromes, immunologic', 'syndromes, immunological deficiency', 'deficiency syndrome, antibody', 'immunological deficiency syndromes', 'syndrome, immunologic deficiency', 'immunological deficiency syndrome', 'syndrome, immunological deficiency', 'antibody deficiency syndromes', 'deficiency syndrome, immunological', 'antibody deficiency syndrome', 'inborn errors of immunity', 'syndrome, antibody deficiency', 'syndromes, antibody deficiency', 'IEI', 'primary immunodeficiency disease', 'deficiency syndrome, immunologic', 'immune deficiency disorder', 'syndromes, immunologic deficiency', 'hypoimmunity', 'deficiency syndromes, antibody', 'deficiency syndromes, immunological', 'primary immunodeficiency', 'immunologic deficiency syndrome']",612,,101997,C0398686,"['0.06155', '-0.1388', '0.0644', '0.62', '0.6753', '0.3044', '0.4155', '0.1567', '-0.4114', '0.07635', '0.0838', '-0.2491', '-0.3647', '0.686', '0.4705', '0.2551', '-0.2722', '0.505', '-1.018', '-0.425', '0.3765', '0.3625', '0.397', '-0.4524', '0.1371', '-0.8857', '-0.573', '-0.2423', '0.0816', '-0.614', '0.143', '0.736', '-0.1694', '-0.3423', '-0.1287', '0.2957', '-0.855', '0.1079', '-0.02798', '-0.0874', '0.262', '0.4185', '-0.1449', '-0.3962', '-0.1765', '-0.642', '-0.1942', '-0.04492', '0.4116', '0.3225', '-0.35', '-0.284', '0.451', '0.02058', '-0.675', '0.1019', '-0.8257', '0.2042', '-0.2947', '-0.587', '-0.01897', '0.355', '0.2764', '0.5005', '0.579', '0.6274', '0.294', '0.614', '-0.3054', '0.8564', '-0.1147', '0.07697', '-0.3225', '-0.5454', '0.3445', '0.1313', '-0.264', '-0.05353', '0.09955', '0.2703', '-0.08496', '0.1048', '0.127', '0.4258', '0.1936', '0.06964', '0.2554', '0.2238', '0.936', '0.1731', '-0.1602', '0.2715', '-0.1382', '-0.287', '0.4238', '1.206', '-0.3284', '-1.111', '-0.1802', '0.364']",C3131,,D007153,279.3,,,
mondo:0003780,T-cell immunodeficiency,"['T-cell immunodeficiency', 'T-lymphocyte deficiency (finding)', 'T-lymphocyte immunodeficiency', 'T lymphocyte deficiency']",613,,,C1274233,,C27145,,,,,,
mondo:0003781,bronchitis,"['acute bronchitis', 'recurrent wheezy bronchitis', 'CI - chest infection', 'chronic bronchitis', 'chest infection', 'acute bronchitis and bronchiolitis', 'bronchus inflammation', 'bronchial infection', 'chest cold']",6132,,,C0006277,,C2911,0009661,D001991,491.9,,,
mondo:0003782,uterine corpus epithelioid leiomyosarcoma,"['body of uterus epithelioid leiomyosarcoma', 'uterine corpus epithelioid leiomyosarcoma', 'uterine epithelioid leiomyosarcoma', 'epithelioid leiomyosarcoma of body of uterus']",6139,,,C1519851,,C40174,,,,,,
mondo:0003783,lymphopenia,"['lymphopenia', 'lymphocytopenia', 'lymphopenia (disease)']",614,,,C0024312,,,,D008231,288.8,D72.810,,0001888
mondo:0003784,nasal cavity carcinoma in situ,"['stage 0 nasal cavity carcinoma aJCC v8', 'nasal cavity in situ carcinoma', 'stage 0 nasal cavity cancer', 'stage 0 nasal cavity carcinoma', 'stage 0 carcinoma of the nasal cavity', 'carcinoma in situ of nasal cavity', 'stage 0 nasal cavity carcinoma aJCC v7', 'stage 0 nasal cavity cancer aJCC v6, v7, and v8', 'stage 0 carcinoma of nasal cavity', 'stage 0 nasal cavity carcinoma aJCC v6', 'carcinoma in situ of nasal cavities', 'carcinoma in situ of the nasal cavity', 'nasal cavity carcinoma in situ']",6148,,,C0347095,,C4589,,,231.8,,,
mondo:0003785,leukopenia,"['leukocytopenia', 'leucopenia', 'White blood cell decreased']",615,,,C0023530,,C26816,0004233,D007970,288.50,,,
mondo:0003786,childhood testicular choriocarcinoma,"['childhood choriocarcinoma of testis', 'paediatric choriocarcinoma of testis', 'pediatric choriocarcinoma of the testis', 'paediatric testicular choriocarcinoma', 'choriocarcinoma of testis of childhood', 'paediatric choriocarcinoma of the testis', 'childhood choriocarcinoma of the testis', 'childhood testicular choriocarcinoma', 'pediatric choriocarcinoma of testis', 'pediatric testicular choriocarcinoma']",6160,,,C1333006,,C6544,,,,,,
mondo:0003787,childhood testicular mixed germ cell cancer,"['pediatric testicular mixed germ cell neoplasm', 'paediatric mixed testicular germ cell cancer', 'pediatric testicular mixed germ cell tumor', 'pediatric mixed testicular germ cell cancer', 'childhood testicular mixed germ cell tumor', 'childhood mixed testicular germ cell cancer', 'paediatric testicular mixed germ cell tumour', 'mixed testicular germ cell cancer of childhood', 'paediatric testicular mixed germ cell neoplasm', 'childhood testicular mixed germ cell tumour', 'childhood testicular mixed germ cell neoplasm']",6161,,,C1333009,,C6542,,,,,,
mondo:0003788,childhood embryonal testis carcinoma,"['pediatric testicular embryonal carcinoma', 'paediatric testicular embryonal carcinoma', 'paediatric embryonal carcinoma of the testis', 'testicular embryonal carcinoma of childhood', 'childhood embryonal carcinoma of testis', 'pediatric embryonal carcinoma of the testis', 'pediatric embryonal carcinoma of testis', 'childhood testicular embryonal carcinoma', 'paediatric embryonal carcinoma of testis', 'childhood embryonal carcinoma of the testis']",6162,,,C1333007,,C6545,,,,,,
mondo:0003789,hereditary papillary renal cell carcinoma,"['hereditary papillary carcinoma of kidney', 'hereditary papillary renal carcinoma', 'renal cell carcinoma, papillary', 'renal cell carcinoma, papillary, 1, familial and somatic', 'hereditary papillary renal cell cancer', 'hereditary papillary carcinoma of the kidney', 'hereditary papillary renal cell carcinoma', 'hereditary kidney papillary carcinoma', 'familial renal papillary carcinoma']",6163,605074,47044,C0879257,"['-0.01906', '0.2183', '0.05826', '-0.11926', '0.0859', '-0.2029', '-0.0397', '0.1683', '0.010086', '-0.1003', '0.0435', '-0.2179', '-0.1772', '-0.09576', '-0.307', '-0.10986', '0.01336', '-0.2021', '0.26', '-0.3367', '-0.1451', '-0.2072', '0.3628', '-0.2673', '0.2391', '0.06274', '-0.10175', '0.03467', '-0.126', '-0.2328', '0.3357', '0.02267', '0.2542', '-0.07196', '-0.164', '-0.1691', '-0.07806', '-0.1223', '-0.11896', '-0.10834', '-0.0712', '-0.1647', '0.368', '-0.325', '0.0826', '-0.3354', '-0.3035', '-0.1295', '0.1086', '-0.1823', '0.1498', '0.01604', '0.02959', '0.02252', '-0.0612', '-0.1399', '0.353', '-0.03069', '-0.6104', '0.0803', '0.363', '0.09595', '-0.02013', '0.02112', '0.1384', '0.0779', '0.3718', '0.4343', '-0.1807', '0.4202', '-0.1626', '-0.1798', '0.05753', '0.10803', '0.3105', '-0.1143', '-0.0745', '0.05545', '-0.08563', '-0.3906', '-0.278', '0.294', '0.11523', '0.0859', '-0.2546', '-0.1506', '0.273', '0.05487', '0.0988', '0.00927', '0.1246', '0.2554', '-0.05347', '-0.2524', '0.4766', '0.10925', '0.3684', '-0.5054', '-0.02007', '0.1288']",C9222,,,,,,
mondo:0003790,prostatic urethra urothelial carcinoma,['prostatic urethra urothelial carcinoma'],6166,,,C1514522,,C39900,,,,,,
mondo:0003791,prostatic urethral cancer,"['prostatic urethra male urethral cancer', 'male urethral cancer of prostatic urethra', 'prostatic urethral malignant neoplasm']",6167,,,C1514523,,C39870,,,,,,
mondo:0003792,ovarian carcinosarcoma,"['malignant mixed mesodermal Müllerian neoplasm of the ovary', 'malignant mixed mesodermal Müllerian tumour of the ovary', 'ovarian MMMT', 'ovarian malignant mesodermal (Mullerian) mixed tumor', 'ovarian malignant mixed mesodermal (Müllerian) tumor', 'malignant mixed mesodermal Mullerian tumor of ovary', 'ovarian malignant mixed mesodermal (Mullerian) tumor', 'ovarian malignant mesodermal (mullerian) mixed tumor', 'malignant mixed mesodermal Mullerian tumor of the ovary', 'malignant mixed mesodermal Müllerian tumor of ovary', 'ovarian malignant mixed Müllerian neoplasm', 'ovarian malignant mixed Mullerian tumor', 'ovarian carcinosarcoma/malignant mixed mesodermal tumour', 'ovarian malignant mesodermal (Müllerian) mixed tumor', 'malignant mixed mesodermal Mullerian neoplasm of the ovary', 'ovarian malignant mixed mesodermal Müllerian neoplasm', 'carcinosarcoma of ovary', 'ovarian malignant mixed mesodermal (Mullerian) tumour', 'carcinosarcoma of the ovary', 'ovarian malignant mixed mesodermal Müllerian tumour', 'ovarian malignant mixed Müllerian tumor', 'ovarian malignant mesodermal (mullerian) mixed tumour', 'ovarian malignant mesodermal (Müllerian) mixed tumour', 'ovarian malignant mixed epithelial mesenchymal tumor', 'malignant mixed mesodermal Müllerian neoplasm of ovary', 'malignant mixed mesodermal Mullerian tumour of ovary', 'ovarian carcinosarcoma', 'ovarian malignant mixed mesodermal Mullerian tumor', 'ovary carcinosarcoma', 'ovarian malignant mixed mesodermal Mullerian tumour', 'malignant mixed mesodermal Mullerian neoplasm of ovary', 'ovarian malignant mixed mesodermal Mullerian neoplasm', 'ovarian malignant mesodermal (Mullerian) mixed tumour', 'MMMT of the ovary', 'malignant mixed mesodermal Müllerian tumor of the ovary', 'malignant mixed mesodermal Mullerian tumour of the ovary', 'ovarian malignant mixed Müllerian tumour', 'ovarian malignant mixed epithelial mesenchymal tumour', 'ovarian malignant mixed Mullerian neoplasm', 'ovarian carcinosarcoma/malignant mixed mesodermal tumor', 'malignant mixed Müllerian tumour of the ovary', 'ovarian malignant mixed mesodermal (Müllerian) tumour', 'malignant mixed Müllerian tumor of the ovary', 'ovarian malignant mixed mesodermal Müllerian tumor', 'malignant mixed mesodermal Müllerian tumour of ovary', 'ovarian malignant mixed Mullerian tumour']",6170,,213512,C0392998,,C9192,1000412,,,,,
mondo:0003795,ovarian small cell carcinoma,"['ovarian small cell NEC', 'SCCO', 'ovarian small cell carcinoma', 'small cell ovarian carcinoma', 'ovary small cell carcinoma', 'small cell carcinoma of ovary', 'small cell carcinoma of the ovary', 'ovarian small cell neuroendocrine carcinoma', 'ovarian small cell cancer']",6179,,370396,C2212006,,C27390,1000431,,,,,
mondo:0003796,rectum Kaposi sarcoma,"['Kaposi^s sarcoma of rectum', 'rectal Kaposi^s sarcoma', 'rectum Kaposi sarcoma', 'rectum Kaposi^s sarcoma', 'rectum Kaposi^s sarcoma (disease)', 'rectal Kaposi sarcoma', 'Kaposi^s sarcoma of the rectum']",6190,,,C1335681,,C5550,,,,,,
mondo:0003799,conjunctivitis,"['Madras eye', 'conjunctiva inflammation', 'pink eye', 'conjunctivitis (disease)', 'conjunctivitis']",6195,,,C0009763,,C34504,,D003231,372.39,,,0000509
mondo:0003800,conventional malignant hemangiopericytoma,['conventional malignant hemangiopericytoma'],6197,,,C1333158,,C9425,,,,,,
mondo:0003801,corneal intraepithelial neoplasm,"['intraepithelial neoplasia of the cornea', 'corneal intraepithelial neoplasia', 'cornea squamous cell intraepithelial neoplasia', 'cornea intraepithelial neoplasia', 'intraepithelial neoplasia of cornea']",6198,,,C1333159,,C6093,,,,,,
mondo:0003802,cornea cancer,"['cancer of cornea', 'malignant tumour of the cornea', 'malignant cornea tumour', 'malignant tumour of cornea', 'corneal tumor', 'malignant cornea tumor', 'malignant corneal tumour', 'corneal tumour', 'malignant cornea neoplasm', 'malignant corneal neoplasm', 'malignant tumor of cornea', 'malignant tumor of the cornea', 'malignant neoplasm of cornea (primary)', 'malignant corneal tumor', 'malignant neoplasm of cornea', 'malignant neoplasm of the cornea', 'cornea cancer']",6199,,,C0153629,,C3565,,,190.4,,,
mondo:0003803,aortic valve disorder,"['aortic valve disease', 'aortic valve disease or disorder', 'aortic valve disorder', 'disorder of aortic valve', 'disease of aortic valve']",62,,,C1260873,,C78650,,,424.1,,,
mondo:0003805,malignant pericardial mesothelioma,"['pericardium mesothelioma', 'pericardium malignant mesothelioma (disease)', 'malignant mesothelioma of the pericardium', 'malignant pericardial mesothelioma', 'malignant mesothelioma of pericardium', 'pericardial malignant mesothelioma', 'pericardial mesothelioma']",6201,,,C1335381,,C7631,,,,,,0100004
mondo:0003806,thyroid hyalinizing trabecular adenoma,"['PLAT', 'thyroid gland hyalinizing trabecular tumour', 'paraganglioma-like adenoma', 'hyalinizing trabecular adenoma of the thyroid', 'hyalinizing trabecular tumor', 'thyroid gland hyalinizing trabecular tumor', 'HTAT', 'thyroid hyalinizing trabecular adenoma', 'hyalinizing trabecular adenoma of thyroid', 'hyalinizing trabecular tumour']",6203,,,C1336751,,C6846,1000588,,,,,
mondo:0003808,mediastinal extraskeletal osteosarcoma,"['osteogenic sarcoma of mediastinum', 'mediastinal extraskeletal osteosarcoma', 'osteogenic sarcoma of the mediastinum', 'osteosarcoma of mediastinum', 'mediastinum osteosarcoma (disease)', 'mediastinal osteosarcoma', 'osteosarcoma of the mediastinum', 'mediastinal osteogenic sarcoma']",6208,,,C1334675,,C6615,,,,,,
mondo:0003809,malignant mediastinum hemangiopericytoma,"['malignant hemangiopericytoma of mediastinum', 'malignant hemangiopericytoma of the mediastinum', 'malignant mediastinal hemangiopericytoma', 'mediastinum hemangiopericytoma', 'mediastinum spindle cell tumour', 'mediastinum spindle cell tumor']",6209,,,C1334598,,C6608,,,,,,
mondo:0003810,bladder diffuse clear cell adenocarcinoma,['bladder diffuse clear cell adenocarcinoma'],6210,,,C1511187,,C39849,,,,,,
mondo:0003811,ovarian seromucinous tumor,"['ovarian Seromucinous tumor', 'mixed epithelial tumour of ovary', 'mixed epithelial tumor of ovary', 'ovarian mixed epithelial tumor', 'mixed epithelial tumor of the ovary', 'mixed epithelial neoplasm of the ovary', 'ovarian Seromucinous tumour', 'ovarian mixed epithelial neoplasm', 'mixed epithelial tumour of the ovary', 'mixed epithelial neoplasm of ovary', 'ovarian mixed epithelial tumour']",6211,,,C0346166,,C4508,1000425,,,,,
mondo:0003812,ovarian endometrial cancer,"['ovarian endometrioid neoplasm', 'ovary endometrioid tumor', 'ovary female reproductive endometrioid cancer', 'endometrioid neoplasm of ovary', 'malignant ovarian endometrioid tumor', 'malignant ovarian endometrioid tumour', 'endometrioid tumour of ovary', 'endometrioid tumor of ovary', 'ovary endometrioid tumour']",6212,,,C1518231,,C40051,,,,,,
mondo:0003813,ovarian papillary tumor,"['papillary tumour of the ovary', 'papillary tumour of ovary', 'ovarian papillary neoplasm', 'papillary neoplasm of the ovary', 'ovarian papillary tumor (morphologic abnormality)', 'ovarian papillary tumour (morphologic abnormality)', 'ovarian papillary tumor', 'papillary tumor of the ovary', 'papillary neoplasm of ovary', 'papillary tumor of ovary']",6214,,,C0476121,,C8430,,,,,,
mondo:0003816,articular cartilage disorder,"['articular cartilage of joint disease or disorder', 'articular cartilage disorder of forearm', 'articular cartilage of joint disease', 'articular cartilage disorder involving pelvic region and thigh', 'articular cartilage disorder involving ankle and foot', 'articular cartilage disorder of the pelvic region and thigh', 'articular cartilage disorder involving upper arm', 'articular cartilage disorder of hand', 'articular cartilage disorder of upper arm', 'articular cartilage disorder involving hand', 'articular cartilage disorder involving multiple sites', 'disease of articular cartilage of joint', 'disorder of articular cartilage of joint', 'articular cartilage disorder of multiple sites', 'articular cartilage disorder involving forearm', 'articular cartilage disorder of shoulder region', 'articular cartilage disorder of ankle and/or foot', 'articular cartilage disorder involving shoulder region']",6227,,,C0158073,,,,,718.02,,,
mondo:0003818,childhood mature teratoma of the ovary,"['paediatric mature teratoma of ovary', 'pediatric mature ovarian teratoma', 'pediatric ovarian mature teratoma', 'childhood mature teratoma of ovary', 'childhood ovarian mature teratoma', 'paediatric ovarian mature teratoma', 'childhood mature ovarian teratoma', 'pediatric mature teratoma of ovary', 'pediatric mature teratoma of the ovary', 'mature ovarian teratoma of childhood', 'paediatric mature ovarian teratoma', 'paediatric mature teratoma of the ovary']",6229,,,C1332991,,C6548,,,,,,
mondo:0003819,childhood teratoma of the ovary,"['pediatric teratoma of ovary', 'childhood teratoma of ovary', 'paediatric teratoma of the ovary', 'paediatric teratoma of ovary', 'childhood teratoma of the ovary', 'paediatric ovarian teratoma', 'ovarian teratoma of childhood', 'childhood ovarian teratoma', 'pediatric teratoma of the ovary', 'pediatric ovarian teratoma']",6230,,,C1332992,,C6554,,,,,,
mondo:0003820,mature ovarian teratoma,"['mature teratoma', 'mature ovarian teratoma', 'mature teratoma of ovary', 'ovary mature teratoma', 'mature teratoma of the ovary']",6231,,,C1334637,,C8112,,,,,,
mondo:0003821,ovarian biphasic or triphasic teratoma,['ovarian biphasic or triphasic teratoma'],6232,,,C1518691,,C39992,,,,,,
mondo:0003822,non-invasive bladder papillary urothelial neoplasm,"['non-invasive bladder papillary urothelial neoplasm', 'papillary urothelial neoplasm of low malignant potential', 'bladder PUNLMP', 'bladder papillary neoplasm of low malignant potential']",6239,,,C1518358,,C39831,,,,,,
mondo:0003824,hereditary kidney oncocytoma,"['hereditary renal oncocytoma', 'familial renal oncocytoma', 'hereditary kidney oncocytoma']",6244,,,C0879606,,C8960,,,,,,
mondo:0003825,kidney oncocytoma,"['oncocytoma of kidney', 'renal epithelial oncocytic tumor', 'oncocytoma renal', 'kidney oncocytic neoplasm', 'renal epithelial oncocytic tumour', 'ROCY', 'kidney oncocytoma', 'oncocytoma kidney', 'renal epithelial oncocytic neoplasm', 'renal oncocytoma', 'oncocytoma of the kidney']",6245,,,C0346255,,C4526,1000315,C537750,,,,
mondo:0003826,mediastinum seminoma,"['seminoma of mediastinum', 'mediastinal seminoma', 'mediastinum seminoma', 'seminoma of the mediastinum']",6249,,,C1334680,,C6812,,,,,,
mondo:0003827,transient hypogammaglobulinemia,,625,,,C0859960,,C27319,,,,,,
mondo:0003828,growth hormone-producing pituitary gland carcinoma,"['malignant somatotropinoma of the pituitary gland', 'malignant Growth hormone secreting neoplasm of the pituitary', 'malignant Somatotrophinoma of pituitary gland', 'malignant Growth hormone secreting neoplasm of pituitary', 'malignant Growth hormone producing pituitary tumor', 'malignant pituitary gland somatotropinoma', 'malignant Growth hormone producing pituitary gland neoplasm', 'malignant Growth hormone producing tumour of the pituitary', 'malignant Growth hormone secreting tumor of the pituitary', 'malignant Growth hormone producing tumor', 'malignant Growth hormone secreting pituitary tumour', 'malignant Growth hormone producing pituitary gland tumor', 'malignant Growth hormone producing tumour of pituitary', 'Growth hormone producing pituitary gland carcinoma', 'malignant Growth hormone producing neoplasm of pituitary', 'malignant Growth hormone producing tumour', 'malignant Growth hormone producing pituitary gland tumour', 'malignant Growth hormone producing neoplasm of pituitary gland', 'malignant Growth hormone producing tumor of the pituitary gland', 'malignant Growth hormone producing tumor of pituitary', 'malignant Growth hormone secreting tumor of pituitary gland', 'malignant somatotropinoma of pituitary gland', 'malignant Growth hormone secreting tumour of pituitary', 'malignant pituitary gland Somatotrophinoma', 'malignant pituitary Somatotrophinoma', 'malignant somatotropinoma of pituitary', 'malignant Growth hormone producing neoplasm of the pituitary gland', 'malignant Growth hormone secreting pituitary tumor', 'malignant Growth hormone producing tumor of the pituitary', 'malignant Growth hormone producing pituitary tumour', 'malignant Growth hormone secreting tumour of the pituitary', 'malignant Growth hormone producing tumour of pituitary gland', 'malignant Somatotrophinoma of the pituitary gland', 'malignant Somatotrophinoma of pituitary', 'malignant Growth hormone secreting tumor of the pituitary gland', 'malignant somatotropinoma of the pituitary', 'malignant Growth hormone secreting tumour of pituitary gland', 'malignant Growth hormone secreting tumor of pituitary', 'malignant Growth hormone secreting pituitary gland tumor', 'malignant Growth hormone secreting pituitary gland tumour', 'malignant Growth hormone producing pituitary neoplasm', 'malignant Growth hormone producing neoplasm of the pituitary', 'malignant Growth hormone secreting neoplasm of pituitary gland', 'malignant Growth hormone secreting neoplasm of the pituitary gland', 'malignant Growth hormone producing tumour of the pituitary gland', 'Growth hormone-producing pituitary gland carcinoma', 'malignant Growth hormone secreting pituitary gland neoplasm', 'malignant pituitary somatotropinoma', 'malignant Growth hormone secreting tumour of the pituitary gland', 'malignant Growth hormone secreting pituitary neoplasm', 'malignant somatotropinoma', 'malignant Growth hormone producing tumor of pituitary gland']",6256,,,C1334587,,C5963,,,,,,
mondo:0003829,chromophil adenoma of the kidney,"['papillary adenoma of the kidney', 'renal papillary adenoma', 'chromophil adenoma of the kidney']",6257,,,C1518879,,C3687,,,,,,
mondo:0003830,type 1 papillary adenoma of the kidney,"['type 1 renal papillary adenoma', 'type 1 papillary adenoma of the kidney']",6258,,,C1519706,,C39809,,,,,,
mondo:0003831,type 2 papillary adenoma of the kidney,"['type 2 renal papillary adenoma', 'type 2 papillary adenoma of the kidney']",6259,,,C1519710,,C39810,,,,,,
mondo:0003832,complement deficiency,"['complement deficiency disease', 'complement activation disease', 'disorder of complement activation', 'immunodeficiency due to a complement cascade component deficiency', 'complement deficiency']",626,,459345,C0272242,,C4691,,,279.8,,,
mondo:0003834,gastric cardia carcinoma,"['carcinoma of the cardia of the stomach', 'carcinoma of cardia of stomach', 'gastric cardia cancer', 'cardia of stomach carcinoma', 'gastric cardia (stomach) cancer', 'carcinoma of gastric cardia', 'cancer of the gastric cardia', 'cancer of gastric cardia', 'carcinoma of the gastric cardia']",6270,,,C1333763,,C6794,1001252,,,,,
mondo:0003835,gastric cardia adenocarcinoma,"['cardia of stomach adenocarcinoma', 'adenocarcinoma of gastric cardia', 'adenocarcinoma of the gastric cardia', 'adenocarcinoma of cardia of stomach', 'adenocarcinoma of the cardia of the stomach']",6271,,,C1333762,,C5247,,,,,,
mondo:0003836,malignant thyroid stimulating hormone producing neoplasm of pituitary gland,"['malignant TSH secreting pituitary tumor', 'malignant TSH secreting pituitary gland neoplasm', 'malignant TSH secreting tumour of the pituitary gland', 'malignant thyroid stimulating hormone producing pituitary gland tumour', 'malignant thyroid stimulating hormone secreting neoplasm of pituitary', 'TSH-producing pituitary gland carcinoma', 'malignant TSH producing pituitary gland tumour', 'malignant TSH secreting pituitary gland tumour', 'malignant TSH producing tumor of the pituitary gland', 'malignant thyroid stimulating hormone secreting neoplasm of pituitary gland', 'malignant thyrotropinoma of the pituitary', 'malignant pituitary thyrotropinoma', 'malignant thyroid stimulating hormone secreting tumor of pituitary gland', 'malignant TSH producing tumour of the pituitary', 'malignant thyroid stimulating hormone secreting pituitary gland tumor', 'malignant thyroid stimulating hormone secreting pituitary tumour', 'malignant thyroid stimulating hormone secreting tumor of pituitary', 'malignant thyroid stimulating hormone secreting pituitary neoplasm', 'malignant thyroid stimulating hormone producing tumor of pituitary', 'malignant thyroid stimulating hormone producing pituitary tumour', 'malignant TSH secreting tumor of the pituitary gland', 'malignant thyroid stimulating hormone producing neoplasm of pituitary gland', 'malignant thyroid stimulating hormone secreting neoplasm of the pituitary gland', 'malignant TSH producing tumor of pituitary gland', 'malignant thyrotropinoma', 'malignant TSH secreting neoplasm of pituitary gland', 'malignant thyroid stimulating hormone secreting tumor of the pituitary gland', 'malignant thyroid stimulating hormone producing tumor of the pituitary gland', 'malignant TSH secreting tumour of pituitary gland', 'malignant TSH secreting pituitary gland tumor', 'malignant thyroid stimulating hormone producing tumour of pituitary gland', 'malignant pituitary gland thyrotropinoma', 'malignant thyrotropinoma of the pituitary gland', 'malignant TSH producing tumor of pituitary', 'malignant TSH producing tumour of pituitary', 'malignant TSH secreting tumour of pituitary', 'malignant TSH producing pituitary tumor', 'malignant thyroid stimulating hormone producing tumor', 'malignant TSH secreting tumor of pituitary', 'malignant thyroid stimulating hormone secreting neoplasm of the pituitary', 'malignant thyroid stimulating hormone secreting pituitary gland neoplasm', 'malignant TSH producing neoplasm of the pituitary', 'malignant thyroid stimulating hormone secreting pituitary gland tumour', 'malignant thyroid stimulating hormone secreting pituitary tumor', 'malignant thyroid stimulating hormone producing neoplasm of pituitary', 'malignant thyroid stimulating hormone producing neoplasm of the pituitary gland', 'malignant TSH secreting pituitary neoplasm', 'malignant thyrotropinoma of pituitary', 'malignant TSH producing neoplasm of pituitary', 'TSH producing pituitary gland carcinoma', 'malignant TSH producing tumour of the pituitary gland', 'malignant thyroid stimulating hormone producing tumour of the pituitary gland', 'malignant TSH producing neoplasm of pituitary gland', 'malignant TSH producing neoplasm of the pituitary gland', 'malignant thyroid stimulating hormone producing tumour of pituitary', 'thyrotropin producing pituitary gland carcinoma', 'malignant TSH secreting neoplasm of the pituitary gland', 'malignant thyroid stimulating hormone producing tumour of the pituitary', 'malignant TSH producing pituitary gland tumor', 'malignant thyroid stimulating hormone secreting tumor of the pituitary', 'malignant TSH producing tumour of pituitary gland', 'malignant TSH secreting tumor of pituitary gland', 'malignant TSH producing pituitary gland neoplasm', 'malignant TSH secreting neoplasm of the pituitary', 'malignant TSH secreting tumour of the pituitary', 'malignant thyroid stimulating hormone producing pituitary neoplasm', 'malignant thyroid stimulating hormone producing tumour', 'malignant TSH secreting tumor of the pituitary', 'malignant thyroid stimulating hormone secreting tumour of the pituitary gland', 'malignant TSH secreting pituitary tumour', 'malignant thyroid stimulating hormone producing pituitary tumor', 'malignant TSH producing pituitary tumour', 'malignant thyroid stimulating hormone producing pituitary gland tumor', 'malignant thyroid stimulating hormone secreting tumour of pituitary gland', 'malignant thyroid stimulating hormone secreting tumour of the pituitary', 'malignant TSH producing tumor of the pituitary', 'malignant TSH secreting neoplasm of pituitary', 'malignant thyroid stimulating hormone producing neoplasm of the pituitary', 'malignant thyroid stimulating hormone secreting tumour of pituitary', 'malignant TSH producing pituitary neoplasm', 'malignant thyroid stimulating hormone producing pituitary gland neoplasm', 'malignant thyroid stimulating hormone producing tumor of the pituitary', 'malignant thyroid stimulating hormone producing tumor of pituitary gland', 'malignant thyrotropinoma of pituitary gland']",6274,,,C1334627,,C5965,,,,,,
mondo:0003837,TSH producing pituitary tumor,"['thyroid stimulating hormone secreting tumour of the pituitary gland', 'thyroid stimulating hormone secreting tumour of pituitary', 'TSH secreting adenoma of the pituitary', 'TSH-producing pituitary gland tumour', 'TSH secreting neoplasm of the pituitary gland', 'TSH secreting tumor of the pituitary gland', 'TSH secreting pituitary gland neoplasm', 'TSH secreting tumour of the pituitary', 'thyroid stimulating hormone producing pituitary gland tumour', 'TSH secreting neoplasm of the pituitary', 'TSH secreting neoplasm of pituitary', 'TSH-producing pituitary gland tumor', 'thyroid stimulating hormone secreting neoplasm of the pituitary', 'thyroid stimulating hormone producing neoplasm of the pituitary gland', 'TSH producing pituitary gland tumour', 'TSH secreting neoplasm of pituitary gland', 'thyroid stimulating hormone producing tumour of the pituitary gland', 'thyroid stimulating hormone producing neoplasm of pituitary', 'thyroid stimulating hormone secreting tumour of the pituitary', 'thyroid stimulating hormone secreting tumor of pituitary', 'TSH producing pituitary gland neoplasm', 'thyroid stimulating hormone secreting pituitary tumour', 'TSH producing tumour of pituitary gland', 'thyrotropin producing pituitary gland neoplasm', 'TSH producing tumour of the pituitary gland', 'TSH secreting tumour of pituitary', 'TSH producing tumor of the pituitary gland', 'TSH producing neoplasm of pituitary', 'thyroid stimulating hormone secreting tumor of the pituitary', 'thyroid stimulating hormone producing pituitary gland tumor', 'thyroid stimulating hormone secreting tumour of pituitary gland', 'thyroid stimulating hormone producing pituitary neoplasm', 'TSH secreting pituitary gland tumor', 'TSH producing neoplasm of pituitary gland', 'thyroid stimulating hormone producing tumor of the pituitary gland', 'TSH secreting pituitary neoplasm', 'thyroid stimulating hormone secreting neoplasm of pituitary', 'thyroid stimulating hormone secreting tumor of the pituitary gland', 'thyroid stimulating hormone secreting neoplasm of pituitary gland', 'thyroid stimulating hormone secreting tumor of pituitary gland', 'thyroid stimulating hormone secreting pituitary gland neoplasm', 'thyroid stimulating hormone producing tumor of pituitary', 'thyroid stimulating hormone secreting pituitary gland tumor', 'TSH secreting tumor of pituitary gland', 'TSH producing tumor of the pituitary', 'thyroid stimulating hormone producing tumor', 'TSH-producing pituitary gland neoplasm', 'thyroid stimulating hormone producing neoplasm of pituitary gland', 'thyroid stimulating hormone producing tumour of the pituitary', 'TSH producing tumour of the pituitary', 'thyroid stimulating hormone producing tumour', 'TSH producing tumour of pituitary', 'TSH secreting pituitary gland tumour', 'TSH producing tumor of pituitary', 'thyroid stimulating hormone producing pituitary gland neoplasm', 'TSH producing pituitary neoplasm', 'thyroid stimulating hormone producing pituitary tumor', 'thyroid stimulating hormone producing neoplasm of the pituitary', 'thyroid stimulating hormone producing tumour of pituitary gland', 'thyroid stimulating hormone secreting pituitary gland tumour', 'TSH producing pituitary tumor', 'TSH secreting tumor of pituitary', 'TSH secreting pituitary tumour', 'thyroid stimulating hormone producing tumor of the pituitary', 'thyroid stimulating hormone secreting pituitary tumor', 'TSH producing neoplasm of the pituitary', 'TSH producing pituitary gland tumor', 'TSH producing tumor of pituitary gland', 'TSH secreting tumor of the pituitary', 'thyroid stimulating hormone producing pituitary tumour', 'thyroid stimulating hormone producing tumor of pituitary gland', 'TSH secreting pituitary tumor', 'TSH secreting tumour of the pituitary gland', 'thyroid stimulating hormone secreting neoplasm of the pituitary gland', 'TSH producing neoplasm of the pituitary gland', 'TSH secreting tumour of pituitary gland', 'thyroid stimulating hormone producing tumour of pituitary', 'thyroid stimulating hormone secreting pituitary neoplasm']",6275,,,C2362538,,C7915,,,,,,
mondo:0003839,ovarian mucinous adenocarcinofibroma,"['ovarian mucinous adenocarcinofibroma', 'ovarian mucinous malignant adenofibroma']",6278,,,C2212014,,C40034,,,,,,
mondo:0003840,epicardium lipoma,"['epicardium lipoma', 'lipoma of the epicardium', 'lipoma of epicardium', 'epicardial lipoma']",6284,,,C1333411,,C6742,,,,,,
mondo:0003841,heart lipoma,"['lipoma of heart', 'heart lipoma', 'lipoma of the heart', 'Cardiac lipoma']",6285,,,C1332849,,C6741,,,,,,
mondo:0003842,childhood cerebellar astrocytic neoplasm,"['cerebellar astrocytoma, childhood', 'paediatric cerebellar astrocytoma', 'cerebellar astrocytoma', 'pediatric astrocytoma of cerebellum', 'pediatric cerebellar astrocytoma', 'childhood astrocytic tumour of cerebellum', 'cerebellum childhood astrocytic tumor', 'paediatric astrocytoma of cerebellum', 'childhood astrocytoma of cerebellum', 'cerebellum childhood astrocytic tumour', 'pediatric astrocytoma of the cerebellum', 'childhood astrocytoma of the cerebellum', 'cerebellum juvenile astrocytoma', 'paediatric astrocytoma of the cerebellum', 'childhood cerebellar astrocytoma', 'childhood astrocytic tumor of cerebellum']",6286,,,C0278594,,C6286,,,,,,
mondo:0003843,cerebral hemisphere lipoma,"['lipoma of the cerebral hemisphere', 'lipoma of cerebral hemisphere', 'cerebral hemisphere lipoma']",6291,,,C1332907,,C6220,,,,,,
mondo:0003844,central nervous system lipoma,"['lipoma of CNS', 'lipoma of the CNS', 'central nervous system lipoma', 'lipoma of central nervous system', 'lipoma of the central nervous system', 'CNS lipoma']",6293,,,C1332885,,C5451,,,,,,
mondo:0003845,corpus callosum lipoma,"['lipoma of the corpus callosum', 'corpus callosum lipoma', 'lipoma of corpus callosum']",6294,,,C1333160,,C5438,,,,,,
mondo:0003846,viral esophagitis,"['Viruses caused esophagitis (disease)', 'viral esophagitis']",6297,,,C0341110,,C27108,,,,,,
mondo:0003847,hereditary disease,"['inherited genetic disease', 'genetic disorder', 'molecular disease', 'genetic condition', 'hereditary disease', 'Mendelian disease', 'hereditary disease or disorder', 'hereditary diseases', 'inherited disease']",630,,,C0019247,,C3101,0000508,D030342,799.89,,,
mondo:0003848,ectopic thymus,['ectopic thymus'],6307,,,C1333375,,C27804,,,,,,
mondo:0003849,clivus chordoma,"['chordoma of the clivus', 'chordoma of clivus', 'clival chordoma', 'clivus of occipital bone chordoma (disease)']",6312,,,C1333071,,C5412,,,170.0,,,
mondo:0003850,clivus chondroid chordoma,"['chondroid chordoma of clivus of occipital bone', 'clivus of occipital bone chondroid chordoma', 'chondroid chordoma of the clivus', 'chondroid chordoma of clivus']",6313,,,C1333072,,C5426,,,,,,
mondo:0003851,ovarian fetiform teratoma,"['ovarian fetiform teratoma', 'homunculus']",6314,,,C1518715,,C39996,,,,,,
mondo:0003852,ovarian solid teratoma,,6315,,,C1335181,,C7285,,,,,,
mondo:0003853,Bartholin gland adenocarcinoma,"['major vestibular gland adenocarcinoma', 'adenocarcinoma of Bartholin^s gland', 'adenocarcinoma of the Bartholin^s gland', 'Bartholin gland adenocarcinoma']",6316,,,C0238016,,C7719,,,,,,
mondo:0003856,adult malignant hemangiopericytoma,"['malignant adult hemangiopericytoma', 'adult hemangiopericytoma, malignant', 'hemangiopericytoma, malignant of adults']",6332,,,C0279547,,C7946,,,,,,
mondo:0003857,adult intracranial malignant hemangiopericytoma,"['adult intracranial solitary fibrous tumor/hemangiopericytoma, grade 3', 'adult malignant intracranial hemangiopericytoma', 'malignant adult intracranial hemangiopericytoma', 'adult intracranial anaplastic hemangiopericytoma', 'central nervous system solitary fibrous tumor/hemangiopericytoma, grade 3']",6333,,,C4331858,,C9183,,,,,,
mondo:0003858,anterior optic tract meningioma,['anterior visual pathway meningioma'],6334,,,C1332308,,C7538,,,,,,
mondo:0003859,bilateral meningioma of optic nerve,"['bilateral optic nerve meningioma', 'bilateral meningioma of the optic nerve']",6335,,,C1332551,,C5304,,,,,,
mondo:0003860,cerebellopontine angle meningioma,"['cerebellopontine angle meningioma (disease)', 'meningioma of C-P angle', 'meningioma of cerebellopontine angle', 'meningioma of the C-P angle', 'meningioma of cerebellar Pontine angle', 'meningioma of the cerebellar Pontine angle', 'C-P angle meningioma', 'meningioma of the cerebellopontine angle', 'cerebellar Pontine angle meningioma']",6337,,,C1263882,,C5300,,,,,,
mondo:0003861,vulvar eccrine adenocarcinoma,"['vulvar eccrine adenocarcinoma', 'eccrine carcinoma of mammalian vulva', 'mammalian vulva eccrine carcinoma']",6339,,,C2202743,,C40305,,,,,,
mondo:0003862,melanotic psammomatous malignant peripheral nerve sheath tumor,"['melanocytic psammomatous malignant peripheral nerve sheath tumour', 'melanocytic psammomatous MPNST', 'melanocytic psammomatous malignant peripheral nerve sheath tumor', 'melanotic psammomatous malignant peripheral nerve sheath tumor']",6344,,,C1513101,,C6910,,,,,,
mondo:0003863,malignant melanocytic neoplasm of the peripheral nerve sheath,"['malignant melanotic peripheral nerve sheath tumour', 'malignant melanotic peripheral nerve sheath tumor', 'melanotic malignant peripheral nerve sheath tumor', 'melanotic malignant nerve sheath tumour', 'melanotic malignant peripheral nerve sheath tumor (morphologic abnormality)', 'melanotic malignant peripheral nerve sheath tumour (morphologic abnormality)', 'melanotic malignant nerve sheath tumor', 'malignant melanocytic peripheral nerve sheath tumour', 'melanocytic MPNST', 'melanotic malignant peripheral nerve sheath tumour', 'malignant melanocytic neoplasm of the peripheral nerve sheath', 'malignant melanocytic peripheral nerve sheath tumor', 'malignant melanocytic neoplasm of peripheral nerve sheath']",6345,,,C0474847,,C4748,,,171.9,,,
mondo:0003864,chronic lymphocytic leukemia/small lymphocytic lymphoma,"['CLL/SLL', 'chronic lymphocytic leukemia/small lymphocytic lymphoma', 'chronic lymphocytic leukemia/small lymphocytic lymphoma (morphologic abnormality)']",6354,,,C1302547,,C27911,,,,,,
mondo:0003865,acral lentiginous melanoma,"['palmar/plantar melanoma', 'acral melanoma', 'ALM', 'acral lentiginous malignant melanoma', 'acral lentiginous melanoma, malignant (morphologic abnormality)', 'malignant acral lentiginous melanoma', 'acral lentiginous melanoma', 'subungual melanoma', 'acral lentiginous malignant melanoma of skin', 'acral lentiginous melanoma, malignant', 'acral lentiginous melanoma (disease)']",6367,,,C0346037,,C4022,,,,,,0012060
mondo:0003866,liver extraskeletal osteosarcoma,"['hepatic osteogenic sarcoma', 'liver osteogenic sarcoma', 'osteosarcoma of the liver', 'hepatic osteosarcoma', 'liver osteosarcoma (disease)', 'liver extraskeletal osteosarcoma', 'osteogenic sarcoma of the liver', 'osteogenic sarcoma of liver', 'osteosarcoma of liver', 'liver osteosarcoma', 'hepatic extraskeletal osteosarcoma']",6370,,,C1333974,,C5833,,,,,,
mondo:0003867,diffuse meningeal melanocytosis,"['diffuse melanocytosis', 'diffuse melanocytosis (morphologic abnormality)', 'meningeal melanocytosis', 'diffuse melanosis']",6379,,,C1266112,,C6890,1000216,,,,,
mondo:0003868,anterior foramen magnum meningioma,"['meningioma of anterior Foramen magnum', 'meningioma of the anterior Foramen magnum']",6381,,,C1332302,,C5281,,,,,,
mondo:0003869,childhood brain stem glioma,"['pediatric glioma of brain stem', 'paediatric glioma of brainstem', 'pediatric brainstem glioma', 'paediatric glioma of brain stem', 'pediatric brain stem glioma', 'paediatric brainstem glioma', 'brain stem glioma of childhood', 'childhood glioma of brainstem', 'childhood glioma of the brainstem', 'paediatric brain stem glioma', 'childhood brainstem glioma', 'pediatric glioma of brainstem', 'childhood glioma of brain stem', 'childhood brain stem glioma', 'brain stem glioma', 'paediatric glioma of the brainstem', 'paediatric glioma of the brain stem', 'pediatric glioma of the brainstem', 'pediatric glioma of the brain stem', 'childhood glioma of the brain stem']",6383,,,C0278600,,C9042,,,,,,
mondo:0003870,childhood brainstem astrocytoma,"['childhood brainstem astrocytoma', 'brain stem astrocytic neoplasm of childhood', 'childhood brain stem astrocytic neoplasm', 'paediatric brain stem astrocytic neoplasm', 'pediatric brain stem astrocytic neoplasm', 'childhood brain stem astrocytoma']",6386,,,C1332950,,C6216,,,,,,
mondo:0003872,ovarian papillary cystadenoma,['ovarian papillary cystadenoma'],6405,,,C1335175,,C7278,,,,,,
mondo:0003873,ovarian surface papilloma,['ovarian surface papilloma'],6407,,,C1335183,,C7279,,,,,,
mondo:0003874,ovarian serous surface papillary adenocarcinoma,"['serous surface papillary carcinoma of ovary', 'ovarian serous surface papillary adenocarcinoma', 'serous surface papillary carcinoma of the ovary', 'ovary papillary carcinoma']",6408,,,C1335178,,C6256,,,,,,
mondo:0003875,childhood central nervous system mature teratoma,"['childhood central nervous system mature teratoma', 'pediatric central nervous system mature teratoma', 'central nervous system mature teratoma of childhood', 'paediatric central nervous system mature teratoma']",6423,,,C1332955,,C27404,,,,,,
mondo:0003876,eyelid carcinoma,"['carcinoma of the eyelid', 'eyelid carcinoma', 'carcinoma of eyelid']",6425,,,C0920196,,C6078,,,,,,
mondo:0003878,malignant choroid melanoma,"['malignant melanoma of the choroid', 'choroidal melanoma', 'melanoma of the choroid', 'choroid malignant melanoma', 'choroid melanoma', 'optic choroid melanoma (disease)', 'melanoma of choroid', 'malignant melanoma of choroid']",6438,,,C0346388,,C4561,,,,,,
mondo:0003879,ovarian endometrioid adenocarcinofibroma,"['ovarian endometrioid malignant adenofibroma', 'ovarian endometrioid adenocarcinofibroma']",6445,,,C1518711,,C40060,,,,,,
mondo:0003880,ceruminous carcinoma,"['carcinoma, ceruminous gland, malignant', 'ceruminous adenocarcinoma (morphologic abnormality)', 'ceruminous adenocarcinoma']",6446,,,C0334353,,C4176,,,,,,
mondo:0003881,vulvar apocrine adenocarcinoma,"['apocrine adenocarcinoma of mammalian vulva', 'vulvar apocrine adenocarcinoma', 'mammalian vulva apocrine adenocarcinoma']",6448,,,C2202741,,C40308,,,,,,
mondo:0003882,central nervous system fibrosarcoma,"['fibrosarcoma of the central nervous system', 'fibrosarcoma of central nervous system', 'CNS fibrosarcoma', 'fibrosarcoma of the CNS', 'central nervous system fibrosarcoma (disease)', 'fibrosarcoma of CNS', 'central nervous system fibrosarcoma']",6451,,,C1332879,,C5465,,,,,,
mondo:0003884,lipoma of the rectum,"['rectum lipoma', 'lipoma of rectum', 'rectal lipoma']",6459,,,C1335684,,C5551,,,,,,
mondo:0003885,colorectal lipoma,"['lipoma of the large intestine', 'lipoma of large bowel', 'colorectal lipoma', 'large intestine lipoma', 'lipoma of large intestine', 'lipoma of the large bowel', 'large bowel lipoma']",6460,,,C1333114,,C5678,,,,,,
mondo:0003886,mucinous cystadenofibroma,['mucinous cystadenofibroma'],6468,,,C1377844,,C8979,,,,,,
mondo:0003887,ovarian mucinous adenofibroma,"['ovarian mucinous adenofibroma', 'mucinous adenofibroma of ovary', 'ovary mucinous adenofibroma']",6469,,,C1518723,,C40040,,,,,,
mondo:0003888,childhood testicular mixed embryonal carcinoma and teratoma,"['pediatric testicular teratocarcinoma', 'childhood teratocarcinoma of the testis', 'childhood testicular teratocarcinoma', 'childhood teratocarcinoma of testis', 'childhood testicular mixed embryonal carcinoma and teratoma', 'paediatric testicular teratocarcinoma']",6474,,,C1333008,,C6539,,,,,,
mondo:0003889,"infiltrating bladder urothelial carcinoma, clear cell variant","['clear cell variant infiltrating bladder urothelial carcinoma', 'infiltrating bladder urothelial carcinoma, clear cell variant']",6476,,,C1512737,,C39827,,,,,,
mondo:0003890,infiltrating bladder urothelial carcinoma,"['invasive transitional cell carcinoma of the urinary bladder', 'invasive bladder transitional cell carcinoma', 'invasive bladder urothelial carcinoma', 'infiltrating transitional cell carcinoma of the urinary bladder', 'infiltrating bladder urothelial carcinoma']",6477,,,C1334281,,C27885,,,,,,
mondo:0003891,bladder signet ring cell adenocarcinoma,"['urinary bladder signet ring cell carcinoma', 'signet Ring cell adenocarcinoma of the urinary bladder', 'signet ring cell adenocarcinoma of bladder', 'signet Ring cell adenocarcinoma of bladder', 'signet Ring cell adenocarcinoma of urinary bladder', 'bladder signet ring cell adenocarcinoma', 'urinary bladder signet Ring adenocarcinoma', 'signet Ring cell adenocarcinoma of the bladder']",6481,,,C1332563,,C6163,,,,,,
mondo:0003892,acinar lung adenocarcinoma,"['acinar adenocarcinoma of the lung', 'acinar lung adenocarcinoma', 'lung acinar adenocarcinoma', 'acinar adenocarcinoma of lung']",6482,,,C1332137,,C5649,,,,,,
mondo:0003893,rete testis adenoma,"['rete testis adenoma', 'adenoma, rete testis, benign']",6483,,,C1514910,,C39956,,,,,,
mondo:0003894,mediastinal melanocytic neurilemmoma,"['melanocytic neurilemmoma of mediastinum', 'melanocytic schwannoma of the mediastinum', 'melanocytic schwannoma of mediastinum', 'melanocytic neurilemmoma of the mediastinum', 'mediastinal melanotic schwannoma', 'mediastinal melanocytic schwannoma']",6484,,,C1334668,,C6635,,,,,,
mondo:0003895,periosteal osteogenic sarcoma,"['PEOS', 'periosteal osteosarcoma (morphologic abnormality)', 'periosteal osteogenic sarcoma', 'periosteal osteosarcoma', 'juxtacortical chondroblastic osteosarcoma']",6489,,,C1377843,,C8970,,,,,,
mondo:0003896,breast capillary hemangioma,"['breast capillary angioma', 'capillary hemangioma of the breast', 'capillary angioma of breast', 'capillary hemangioma of breast', 'breast capillary hemangioma', 'capillary angioma of the breast']",6491,,,C1332619,,C5210,,,,,,
mondo:0003897,breast epithelioid hemangioma,"['epithelioid hemangioma of the breast', 'epithelioid hemangioma of breast', 'breast epithelioid hemangioma', 'histiocytoid hemangioma of breast', 'epithelioid breast hemangioma', 'histiocytoid hemangioma of the breast', 'breast histiocytoid hemangioma', 'histiocytoid breast hemangioma']",6492,,,C1332627,,C5211,,,,,,
mondo:0003898,pediatric myxoid chondrosarcoma,"['childhood myxoid chondrosarcoma', 'myxoid chondrosarcoma of childhood', 'pediatric myxoid chondrosarcoma']",6494,,,C1332984,,C27377,,,,,,
mondo:0003899,adult myxoid chondrosarcoma,"['myxoid chondrosarcoma of adults', 'adult myxoid chondrosarcoma']",6495,,,C1332209,,C27378,,,,,,
mondo:0003900,connective tissue disorder,"['connective tissue disorders', 'connective tissue disorder', 'connective tissue disease or disorder', 'disease, connective tissue', 'primary disorder of connective tissue', 'disorder of connective tissue', 'tissue disease, connective', 'disease of connective tissue', 'connective tissue diseases', 'connective tissue disease']",65,,,C0009782,,C26729,,D003240,,,,
mondo:0003901,cerebellar hemangioblastoma,"['cerebellar hemangioblastoma', 'cerebellar angioblastoma', 'angioblastoma of cerebellum', 'cerebellum hemangioblastoma', 'angioblastoma of the cerebellum', 'hemangioblastoma of the cerebellum', 'hemangioblastoma of cerebellum', 'cerebellar capillary hemangioblastoma']",6500,,,C1332900,,C5146,,,,,,
mondo:0003902,brain stem hemangioblastoma,"['hemangioblastoma of the brainstem', 'brainstem hemangioblastoma', 'angioblastoma of brainstem', 'hemangioblastoma of brain stem', 'brainstem angioblastoma', 'angioblastoma of brain stem', 'angioblastoma of the brainstem', 'brain stem capillary hemangioblastoma', 'brain stem hemangioblastoma', 'angioblastoma of the brain stem', 'hemangioblastoma of the brain stem', 'brain stem angioblastoma', 'hemangioblastoma of brainstem']",6501,,,C1332611,,C5147,,,,,,
mondo:0003903,benign vaginal mixed tumor,"['vaginal spindle cell epithelioma', 'benign vaginal mixed tumor']",6505,,,C1511107,,C40280,,,,,,
mondo:0003904,lung occult squamous cell carcinoma,"['occult squamous cell carcinoma of lung', 'occult squamous cell carcinoma of the lung', 'occult squamous cell lung carcinoma']",6510,,,C1335100,,C6686,,,,,,
mondo:0003905,"ovarian yolk sac tumor, glandular pattern","['glandular pattern ovarian yolk sac tumor', 'ovarian yolk Sac tumor, glandular pattern', 'glandular pattern ovarian yolk sac tumour']",6511,,,C1518747,,C39988,,,,,,
mondo:0003906,"ovarian yolk sac tumor, hepatoid pattern","['hepatoid pattern ovarian yolk sac tumor', 'ovarian yolk Sac tumor, hepatoid pattern', 'hepatoid pattern ovarian yolk sac tumour']",6512,,,C1518748,,C39989,,,,,,
mondo:0003907,"ovarian yolk sac tumor, polyvesicular vitelline pattern","['polyvesicular vitelline pattern ovarian yolk sac tumour', 'ovarian yolk sac tumor, polyvesicular vitelline pattern', 'polyvesicular vitelline pattern ovarian yolk sac tumor']",6514,,,C1518749,,C39987,,,,,,
mondo:0003908,clivus meningioma,"['meningioma of the clivus', 'meningioma of clivus', 'clivus of occipital bone meningioma (disease)']",6517,,,C1333073,,C5289,,,,,,
mondo:0003909,Bartholin gland adenomyoma,"['Bartholin gland adenomyoma', 'adenomyoma of major vestibular gland', 'major vestibular gland adenomyoma']",6518,,,C1511049,,C40300,,,,,,
mondo:0003910,mixed cell uveal melanoma,['mixed cell uveal melanoma'],6522,,,C1334782,,C35781,1000380,,,,,
mondo:0003911,ciliary body mixed cell melanoma,"['mixed cell uveal melanoma of ciliary body', 'ciliary body mixed cell uveal melanoma', 'ciliary body mixed cell melanoma']",6523,,,C1333051,,C35783,,,,,,
mondo:0003912,malignant ciliary body melanoma,"['melanoma of ciliary body', 'ciliary body malignant melanoma', 'malignant melanoma of the ciliary body', 'ciliary body melanoma', 'melanoma of the ciliary body', 'malignant melanoma of ciliary body', 'ciliary body melanoma (disease)']",6524,,,C0346379,,C4558,,,190.8,,,
mondo:0010169,Usher syndrome type 2A,"['US2', 'USHER syndrome, type IIA', 'retinal disease in usher syndrome type IIA, modifier of', 'Usher syndrome caused by mutation in USH2A', 'Usher syndrome type IIA', 'USH2A Usher syndrome', 'USH2A', 'Usher syndrome, type 2A']",0110838,276901,,C1848634,,,,C536490,,H35.5,,
mondo:0010170,Usher syndrome type 3A,"['Usher syndrome, type 3A', 'Usher syndrome, type 3', 'USH3A', 'Usher syndrome caused by mutation in CLRN1', 'USHER syndrome, type IIIA', 'Usher syndrome type IIIA', 'CLRN1 Usher syndrome']",0110841,276902,,,,,,,,H35.5,,
mondo:0010171,Usher syndrome type 1C,"['Usher syndrome, type 1C', 'Usher syndrome type IC', 'USH1C', 'Usher syndrome, type I, Acadian variety', 'Usher syndrome, Acadian variety', 'Usher syndrome type I Acadian variety', 'USHER syndrome, type IC']",0110830,276904,,C1848604,,,,,,H35.5,,
mondo:0010172,VACTERL with hydrocephalus,"['VACTERL-H', 'VACTERL hydrocephaly', 'VACTERL association with hydrocephalus', 'Sujansky-Leonard syndrome', 'Vater association with macrocephaly and ventriculomegaly', 'vertebral (V), anal (A), cardiac (C), tracheoesophageal (te), renal (R) and limb (L) anomalies and hydrocephaly', 'Vater association with hydrocephalus', 'VACTERL association with hydrocephaly']",,276950,3412,C1848599,"['-0.2156', '-0.2388', '0.09534', '0.2947', '-0.06866', '-0.2468', '-0.3403', '0.534', '-0.3022', '0.5586', '-0.1863', '-0.783', '-0.5005', '0.4175', '0.3218', '-0.1157', '-0.552', '-0.06094', '-0.793', '-1.156', '-0.02002', '-0.0954', '0.2698', '-0.2688', '-0.3396', '-0.679', '-0.863', '0.829', '-0.1619', '0.4653', '-0.2896', '-0.9375', '0.647', '-0.2023', '-0.2937', '0.5454', '-0.0002644', '-0.001752', '0.09467', '-0.2072', '0.822', '0.5596', '0.04977', '-0.778', '0.9297', '-0.09894', '0.5195', '-0.5405', '0.272', '0.428', '0.2438', '-0.02557', '-0.2448', '-1.081', '0.2617', '-0.3477', '-0.07526', '0.296', '-0.05368', '0.3372', '-0.2268', '0.516', '-0.525', '-0.123', '0.1338', '0.2444', '0.1472', '-0.05814', '-1.018', '0.0918', '-0.3806', '1.071', '0.12494', '-0.846', '0.2219', '0.3816', '0.324', '0.8315', '-0.3445', '-1.069', '-0.2471', '-0.0631', '-0.3525', '0.5376', '0.2491', '1.01', '0.5576', '0.1869', '0.4082', '-0.5166', '-0.243', '0.8193', '0.27', '0.0433', '0.7876', '0.4028', '0.5757', '-0.3232', '-0.00569', '0.3486']",,,,,,,
mondo:0010173,Mayer-Rokitansky-Kuster-Hauser syndrome type 1,"['Mayer-Rokitansky-KUSTER-Hauser syndrome', 'Mullerian dysgenesis', 'Müllerian agenesis', 'Mayer-Rokitansky-Küster-Hauser syndrome type 1', 'Rokitansky syndrome', 'MRKH syndrome', 'genital renal ear syndrome', 'Von Mayer-Rokitansky-Kuster anomaly', 'congenital absence of uterus and vagina', 'urogenital adysplasia', 'MRKH syndrome type 1', 'uterus Bipartitus solidus Rudimentarius cum vagina Solida', 'Mrk anomaly', 'MRKH anomaly', 'congenital absence of the uterus and vagina (CAUV)', 'Mullerian aplasia/dysgenesis', 'Mayer-Rokitansky-Kuster-Hauser syndrome (MRKH)', 'Rokitansky sequence']",0112178,277000,247775,,,,,,752.49,,,
mondo:0010174,Valinemia,"['valine transaminase deficiency', 'hypervalinemia', 'Valinemia']",,277100,,C0268573,,,,C536524,,,,
mondo:0010175,van Bogaert-Hozay syndrome,"['A familial form of acro-osteolysis associated with a mild mental retardation, skin atrophy, facial dysmorphism, and ocular defects', 'Hozay^s syndrome', 'A familial form of acro-osteolysis associated with a mild intellectual disability, skin atrophy, facial dysmorphism, and ocular defects', 'Hozay’s syndrome', 'van Bogaert-Hozay syndrome', 'acro-osteolysis-facial dysplasia syndrome']",,277150,,C1848598,,,,C536526,,,,
mondo:0010176,orofaciodigital syndrome type 6,"['Joubert syndrome with oral-facial-digital syndrome', 'Varadi syndrome', 'Váradi syndrome', 'orofaciodigital syndrome VI', 'Váradi-Papp syndrome', 'oral-Facial-digital syndrome, type 6', 'Varadi-Papp syndrome', 'orofaciodigital syndrome type 6', 'polydactyly-cleft lip/palate-psychomotor retardation syndrome', 'Ofds 6', 'polydactyly, cleft Lip/palate or lingual lump, and psychomotor retardation', 'Joubert syndrome with orofaciodigital defect', 'OFD6', 'polydactyly - cleft lip/palate - psychomotor retardation', 'oral-facial-digital syndrome type 6', 'orofaciodigital syndrome 6', 'polydactyly cleft lip palate psychomotor retardation']",0060376,277170,2754,C2745997,"['0.2246', '-0.1996', '-0.015175', '-0.2494', '-0.277', '-0.294', '-0.3188', '-0.10535', '-0.2583', '-0.4988', '-0.06647', '-0.5103', '-0.1764', '-0.4', '0.04916', '-0.0772', '0.4685', '-0.5435', '-0.08527', '-1.23', '0.10144', '0.2145', '0.7227', '-0.4216', '0.3455', '0.3745', '-0.9097', '0.1235', '0.7095', '-0.5913', '0.4915', '0.0769', '0.3247', '0.6006', '0.3252', '-0.427', '-0.013885', '0.01087', '-0.5786', '0.1559', '0.4678', '-0.4316', '0.001149', '0.1157', '0.4285', '-0.527', '0.02046', '0.6294', '0.06604', '0.285', '-0.3442', '0.2676', '-0.341', '-0.2925', '-0.718', '-0.2201', '0.0989', '-0.1471', '0.0225', '0.5957', '0.3298', '0.09015', '0.1763', '0.05948', '-0.1619', '-0.1566', '0.2308', '-0.09625', '-0.714', '0.843', '-0.5767', '0.4172', '0.0846', '-0.00278', '0.3955', '0.2246', '-0.07275', '-0.4077', '-0.5938', '-0.0345', '0.1422', '0.1098', '0.1938', '0.3762', '-0.1203', '-0.1414', '-0.3894', '0.8745', '0.01479', '-0.0004199', '-0.04776', '-0.00595', '0.3123', '-0.1401', '0.481', '-0.2179', '0.252', '-0.2119', '0.299', '0.546']",C124841,,C536531,,,,
mondo:0010177,vascular hyalinosis,"['digestive tract and renal small vessel hyalinosis, intracerebral calcifications, retinal ischemic syndrome and phenotypic a', 'retinal ischaemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome', 'digestive tract and renal small vessel hyalinosis, intracerebral calcifications, retinal ischaemic syndrome and phenotypic a', 'vascular hyalinosis', 'Rambaud-Gallian-Touchard syndrome', 'retinal ischemic syndrome-digestive tract small vessel hyalinosis-diffuse cerebral calcifications syndrome', 'Rambaud-Gallian syndrome']",,277175,3018,,,,,C564750,,,,
mondo:0010178,congenital bilateral aplasia of vas deferens from CFTR mutation,"['congenital bilateral aplasia of the vas deferens', 'vas deferens, congenital bilateral aplasia of', 'CAVD', 'congenital bilateral absence of vas deferens', 'CBAVD']",0111864,277180,,,,C129303,,,,,,
mondo:0010179,isolated right ventricular hypoplasia,"['right ventricle hypoplasia', 'right ventricular hypoplasia, isolated', 'Irvh', 'hypoplasia of the right ventricle', 'isolated hypoplasia of the right ventricle', 'right ventricular hypoplasia']",,277200,439,C1848587,,,,C535682,,,,
mondo:0010180,autosomal recessive spondylocostal dysostosis,"['spondylocostal dysostosis, autosomal recessive', 'Jarcho-Levin syndrome', 'spondylocostal dysostosis 1, autosomal recessive', 'costovertebral dysplasia', 'SCDO1']",,,2311,CN032975,"['-0.5444', '0.3845', '0.2168', '-0.75', '0.1653', '-0.2788', '0.4114', '0.6846', '-0.509', '-0.694', '-0.013855', '-0.09436', '-0.3162', '-0.04648', '-0.1501', '0.2952', '-0.0682', '-0.0392', '-1.052', '-0.8066', '-0.2333', '0.7773', '0.8438', '0.175', '0.1395', '-0.1597', '0.06183', '0.2047', '0.2134', '-0.3665', '0.2761', '-0.4138', '0.2708', '0.1578', '0.05634', '-0.3618', '0.1282', '-0.658', '-0.02861', '0.006733', '-0.523', '0.00785', '0.7354', '-0.0867', '-0.03284', '-0.65', '-0.2717', '0.07874', '0.05112', '0.342', '-0.03775', '-0.2241', '0.1735', '-0.0813', '-0.8745', '-0.506', '-0.483', '0.3677', '0.4446', '-0.06287', '0.02965', '0.491', '-0.3633', '0.2632', '0.3909', '-0.03574', '0.4705', '0.4028', '-0.4258', '-0.05447', '-0.2467', '0.07404', '-0.000691', '0.10455', '-0.2089', '0.374', '0.2559', '-0.1577', '-0.3005', '0.1188', '-0.2944', '0.2488', '0.2903', '0.706', '-0.3926', '0.12274', '0.225', '-0.05945', '-0.1371', '0.3054', '-0.3977', '-0.2225', '0.2292', '-0.38', '0.502', '0.1564', '0.7104', '-0.6035', '0.1406', '-0.00669']",,,C535781,756.9,,,
mondo:0010181,oculogastrointestinal muscular dystrophy,"['visceral myopathy - familial external ophthalmoplegia', 'intestinal pseudoobstruction with external ophthalmoplegia', 'familial visceral myopathy with external ophthalmoplegia', 'muscular dystrophy, oculogastrointestinal', 'visceral myopathy, familial, with external ophthalmoplegia', 'visceral myopathy-familial external ophthalmoplegia syndrome']",,277320,1876,,,,,,,G71.0,,
mondo:0010182,"hypercarotenemia and vitamin A deficiency, autosomal recessive","['hypercarotenemia and vitamin A deficiency, autosomal recessive']",,277350,,C2678266,,,,C567486,,,,
mondo:0010183,methylmalonic aciduria and homocystinuria type cblF,"['methylmalonic aciduria due to vitamin B12-release defect', 'methylmalonic acidemia and homocystinuria, cblF type', 'methylmalonic aciduria and homocystinuria, cblF type', 'methylmalonic acidemia with homocystinuria type cblF', 'cblF defect', 'lysosomal membrane cobalamin transporter deficiency', 'cobalamin, defect in lysosomal release of', 'vitamin B12 storage disease', 'cobalamin F disease', 'cobalamin F defect', 'combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblF', 'MAHCF', 'methylmalonic aciduria with homocystinuria, type cblF', 'cobalamin F deficiency', 'vitamin B12 lysosomal release defect']",0050717,277380,79284,,"['0.1304', '0.3599', '0.01428', '-0.4492', '0.3198', '-0.5376', '-0.474', '0.4521', '-0.2484', '-0.002457', '-0.5337', '-0.1864', '-0.1683', '-0.1855', '-0.01694', '-0.10455', '0.154', '-0.1925', '-0.3684', '-0.4917', '-0.1065', '-0.3296', '-0.01267', '-0.3364', '0.3481', '-0.10803', '0.0329', '-0.01162', '0.1721', '-0.197', '-0.1827', '0.2174', '0.1885', '0.2534', '-0.1854', '-0.03772', '-0.442', '-0.662', '-0.3845', '0.056', '-0.07135', '-0.453', '0.3013', '-0.0725', '-0.6016', '-0.4202', '0.1465', '-0.1539', '-0.00903', '0.2642', '-0.1449', '-0.0955', '-0.3452', '-0.08527', '0.2367', '-0.1368', '0.217', '0.2722', '-0.3882', '0.5513', '-0.01613', '0.0677', '0.1718', '-0.6353', '0.2001', '-0.10645', '0.4973', '0.553', '-0.556', '0.0674', '-0.0944', '-0.2037', '-0.1898', '-0.4492', '0.2367', '0.4026', '0.2267', '-0.496', '-0.06094', '0.1873', '0.6826', '0.03827', '-0.2378', '0.1062', '0.6406', '0.2659', '-0.01526', '0.8433', '0.7935', '0.535', '0.3328', '0.7974', '0.4038', '-0.2825', '0.3984', '1.071', '0.4182', '-0.0532', '0.3696', '0.05515']",,,C564747,,,,
mondo:0010184,methylmalonic aciduria and homocystinuria type cblC,"['cblC defect', 'methylmalonic aciduria and homocystinuria cblC', 'combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblC', 'cblC', 'methylmalonic acidemia with homocystinuria, type cblC', 'methylmalonic aciduria with homocystinuria, type cblC', 'MAHCC', 'methylmalonic aciduria and homocystinuria, cblC type', 'methylmalonic aciduria and homocystinuria, vitamin B12-responsive', 'vitamin B12 metabolic defect with combined deficiency of methylmalonyl-Coa mutase and homocysteine:methyltetrahydrofolate methyltransferase', 'methylmalonic acidemia and homocystinuria cblC', 'methylmalonic acidemia and homocystinuria, cblC type', 'methylmalonic aciduria and homocystinuria, cblC type, digenic', 'cobalamin C defect', 'methylmalonic acidemia with homocystinuria type cblC', 'cobalamin C deficiency']",0050715,277400,79282,CN205878,"['0.1305', '0.2216', '0.277', '-0.5103', '0.3203', '-0.5103', '-0.3909', '0.1945', '-0.3313', '0.11743', '-0.608', '-0.4841', '-0.2876', '-0.6216', '-0.0844', '-0.3462', '-0.2083', '-0.4363', '-0.4878', '-0.4148', '0.1627', '-0.596', '-0.0761', '-0.4326', '0.4758', '-0.1769', '0.03635', '-0.368', '-0.04324', '-0.1738', '-0.2737', '0.2393', '0.523', '-0.0426', '-0.03513', '0.2246', '-0.6157', '-0.6304', '-0.3337', '-0.04828', '0.0817', '-0.563', '0.4292', '0.3516', '-0.3955', '-0.4004', '-0.06183', '-0.2344', '0.2181', '-0.05496', '0.2827', '0.163', '-0.2632', '-0.1913', '0.08484', '-0.279', '0.617', '0.0652', '-0.612', '0.538', '-0.01027', '-0.0354', '0.3533', '-0.4724', '0.02821', '-0.01172', '0.4724', '0.2458', '-0.3853', '0.2383', '-0.05496', '0.01958', '-0.2166', '-0.2208', '-0.1497', '0.479', '0.1289', '-0.3298', '-0.06088', '0.2164', '0.614', '-0.422', '-0.4165', '0.1075', '0.529', '0.2302', '8.935e-05', '0.946', '0.6357', '0.5986', '0.3762', '0.613', '0.3218', '-0.08984', '0.587', '1.071', '0.4846', '-0.2091', '0.328', '0.0814']",C142174,,,,,,
mondo:0010185,methylmalonic aciduria and homocystinuria type cblD,"['methylmalonic acidemia with homocystinuria type cblD', 'methylmalonic acidemia and homocystinuria, cblD type', 'methylmalonic acidemia, Cblh type, formerly', 'cblD defect', 'methylmalonic acidemia, Cblh type', 'MAHCD', 'methylmalonic acidemia with homocystinuria, type cblD', 'methylmalonic aciduria and homocystinuria, cblD type', 'homocystinuria, cblD type, variant 1', 'methylmalonic aciduria, Cblh type', 'Mehtylmalonic acidemia with homocystinuria cbI d', 'methylmalonic aciduria, cblD type, variant 2, included', 'methylmalonic aciduria, Cblh type, formerly', 'methylmalonic aciduria, cblD type, variant 2', 'homocystinuria, cblD type, variant 1, included', 'methylmalonic aciduria with homocystinuria, type cblD', 'cobalamin D defect', 'cobalamin D deficiency', 'combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblD']",0050716,277410,79283,CN205879,"['-0.01772', '0.1038', '0.000349', '0.00546', '0.03778', '-0.0847', '-0.02841', '0.05728', '-0.0641', '0.03952', '-0.1522', '-0.07776', '0.03488', '-0.0202', '-0.0713', '-0.1538', '-0.05045', '-0.06274', '-0.02808', '-0.1996', '-0.0006394', '-0.1578', '0.11273', '-0.05795', '0.1036', '-0.01036', '0.002295', '-0.1295', '-0.01855', '-0.08716', '-0.001894', '0.05283', '0.0673', '0.0891', '0.05103', '-0.0749', '-0.010216', '-0.1733', '-0.01898', '-0.0671', '0.010315', '-0.2384', '0.0541', '-0.0176', '-0.09875', '-0.1832', '0.03568', '0.121', '-0.07294', '0.05103', '-0.0695', '-0.1315', '-0.01001', '-0.001965', '-0.12213', '-0.05865', '0.2075', '-0.07684', '-0.1825', '0.1504', '0.1282', '0.00864', '0.0709', '-0.06445', '0.01478', '-0.008446', '0.1836', '0.002047', '-0.11206', '0.11053', '0.004345', '-0.002907', '-0.05865', '-0.209', '0.0579', '0.1495', '-0.03333', '-0.2128', '-0.0863', '-0.00503', '0.10443', '-0.04636', '-0.12054', '0.1061', '0.0443', '0.05777', '-0.04105', '0.1498', '0.2725', '0.0745', '0.12335', '0.12213', '0.0463', '-0.02719', '0.2284', '0.1646', '0.1355', '-0.1707', '-0.0755', '0.04404']",,,C564743,,,,
mondo:0010186,"vitamin D-dependent rickets, type 2A","['vitamin D receptor deficiency rickets', 'vitamin D dependent rickets 2a', 'vitamin D-dependent rickets, type 2 caused by mutation in VDR', 'vitamin D-resistant rickets with end-organ unresponsiveness to 1,25-dihydroxycholecalciferol', 'rickets, vitamin D-resistant, type IIA', 'Pseudovitamin D-deficiency, type 2A', 'rickets-alopecia syndrome', 'generalised resistance to 1,25-dihydroxyvitamin D', 'VDR vitamin D-dependent rickets, type 2', 'hereditary 1,25 dihydroxyvitamin D-resistant rickets with abnormal vitamin D receptor with alopecia', 'generalized resistance to 1,25-dihydroxyvitamin D', 'rickets, hereditary vitamin D-resistant', 'vitamin D-dependent rickets, type 2A, with or without alopecia', 'VDDR2A', 'Pddr 2A', 'hypocalcemic vitamin D-resistant rickets', 'vitamin D-dependent rickets, type 2A', 'vitamin d-dependent rickets type II with alopecia']",0080884,277440,,C0342646,,C131075,,C562794,,,,
mondo:0010187,"vitamin K-dependent clotting factors, combined deficiency of, type 1","['multiple coagulation Factor deficiency 3', 'VKCFD1', 'hereditary combined deficiency of factors II, VII, IX and X', 'familial multiple coagulation Factor deficiency 3', 'vitamin K-dependent clotting factors, combined deficiency of, type 1', 'glutamic acid, deficient gamma-carboxylation of', 'GGCX congenital vitamin K-dependent coagulation factors combined deficiency', 'FMFD 3', 'Vkcfd', 'vitamin K-dependent coagulation defect', 'congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in GGCX', 'vitamin K-dependent clotting factors, combined deficiency of, 1', 'hereditary combined deficiency of vitamin K-dependent clotting factors', 'factors II, VII, IX, and X, combined deficiency of']",0112173,277450,,C1848534,,,,C564741,,,,
mondo:0010188,familial isolated deficiency of vitamin E,"['ataxia with isolated vitamin E deficiency', 'Friedreich-like ataxia', 'VED', 'AVED', 'ataxia with vitamin E deficiency', 'familial isolated vitamin E deficiency', 'ataxia, Friedreich-like, with selective vitamin E deficiency', 'vitamin E, familial isolated deficiency OF', 'isolated vitamin E deficiency', 'familial isolated deficiency of vitamin type E', 'Friedreich-like ataxia with selective vitamin E deficiency']",0090028,277460,96,,"['0.2336', '-0.3674', '-0.8887', '0.0924', '0.3643', '-0.4177', '-0.1804', '0.594', '-0.5312', '-0.2032', '0.4124', '0.4014', '-0.163', '-0.4814', '0.458', '-0.6787', '-0.1827', '-0.578', '-0.3389', '-0.6865', '0.2722', '-0.3738', '0.1758', '0.2198', '0.3394', '0.3765', '-0.1667', '-0.3716', '-0.4368', '0.03632', '0.1221', '-0.111', '-0.00825', '-0.03915', '-0.4595', '-0.2334', '-0.09155', '-0.7446', '-0.1058', '0.175', '-0.1847', '-0.4429', '0.01953', '0.3198', '0.378', '-0.3564', '0.1735', '0.4214', '-0.069', '-0.1478', '0.3174', '0.02657', '-0.3875', '-0.474', '0.1893', '0.3706', '0.3933', '-0.3547', '-1.009', '0.2335', '-0.391', '0.000924', '0.0819', '0.0802', '0.0688', '0.08057', '0.4644', '0.3552', '0.1025', '0.2964', '-0.281', '0.09033', '0.2961', '-0.8096', '0.535', '0.2106', '0.3416', '-0.5615', '0.492', '-0.3728', '0.3704', '-0.4355', '-0.06335', '0.729', '-0.003096', '0.1716', '-0.534', '0.04282', '0.451', '-0.03937', '0.665', '0.000917', '-0.0942', '0.0924', '-0.0404', '0.827', '0.342', '-0.1288', '-0.1741', '0.1114']",,,C535393,334.3,,10047631,
mondo:0010189,"vitiligo, progressive, with intellectual disability and urethral duplication","['vitiligo, progressive, with intellectual disability and urethral duplication', 'vitiligo, progressive, with mental retardation and urethral duplication']",,277465,,C1848532,,,,C564739,,,,
mondo:0010190,pontocerebellar hypoplasia type 2A,"['pontocerebellar hypoplasia with progressive cerebral atrophy', 'Volendam neurodegenerative disease', 'microcephaly pontocerebellar hypoplasia dyskinesia', 'pontocerebellar hypoplasia type 2 caused by mutation in TSEN54', 'TSEN54 pontocerebellar hypoplasia type 2', 'PCH2A', 'pontocerebellar hypoplasia, type 2A', 'Pch2']",0060267,277470,,,,,,C564738,,,,
mondo:0010191,von Willebrand disease 3,"['von Willebrand disease type III', 'von Willebrand^s disease 3', 'VON WILLEBRAND disease, type 3', 'VWD3', 'von Willebrand^s disease type 3', 'VWD type 3', 'Von Willebrand disease, type 3', 'von Willebrand disease type 3', 'VWD, type 3']",0111054,277480,166096,C1264041,"['-0.2595', '0.319', '-0.7783', '0.1361', '-0.3318', '-0.0655', '-0.127', '0.3662', '0.2905', '-0.826', '-0.134', '0.4429', '0.5713', '0.7114', '-0.3936', '-0.4563', '0.3386', '-0.0748', '-0.4539', '-0.541', '-0.4922', '-1.063', '1.125', '0.1555', '-0.3938', '0.2319', '-0.3772', '0.1476', '0.58', '0.012276', '0.7935', '0.01472', '0.0758', '0.3328', '0.2874', '-0.406', '-0.182', '-0.2074', '0.2041', '-0.0362', '0.2627', '-0.3005', '0.1736', '-0.684', '0.4695', '0.219', '-0.7666', '0.01141', '0.0986', '0.006218', '0.618', '-0.1843', '0.3445', '-0.184', '-0.2003', '-0.1787', '-0.7495', '0.566', '-0.758', '0.002426', '-0.6133', '0.0909', '0.6597', '-0.8066', '0.5757', '-0.1781', '0.13', '-0.4626', '-0.8633', '0.2637', '-0.2805', '-0.0916', '-0.2961', '-0.9443', '1.178', '0.5806', '0.957', '0.426', '0.2976', '-0.19', '-0.4888', '-0.2996', '1.025', '-0.2712', '-0.12024', '0.201', '0.1313', '0.5664', '0.1448', '-0.2793', '-0.207', '0.582', '-0.3281', '-0.1554', '0.8794', '0.744', '0.02452', '-0.9365', '-0.2666', '-0.1523']",C85213,,D056729,,,,
mondo:0010192,Waardenburg syndrome type 4A,"['EDNRB Waardenburg syndrome', 'Waardenburg syndrome caused by mutation in EDNRB', 'Waardenburg syndrome type IVA', 'Waardenburg syndrome with Hirschsprung disease type 4A', 'Waardenburg syndrome with Hirschsprung disease, type 4A', 'Waardenburg syndrome, type 4A', 'WS4A', 'Waardenburg-Shah syndrome', 'Ws4', 'Shah-Waardenburg syndrome']",0110953,277580,,,,,,,,,,
mondo:0010193,Weaver syndrome,"['WEAVER syndrome', 'Weaver syndrome', 'WEAVER-like syndrome', 'Weaver Williams syndrome', 'Weaver-like syndrome', 'overgrowth syndrome with accelerated skeletal maturation, unusual facies, and camptodactyly', 'intellectual disability, microcephaly, weight deficiency, unusual facies, clinodactyly, bone hypoplasia, and cleft palate', 'EZH2 related overgrowth', 'Weaver Smith syndrome', 'camptodactyly - overgrowth - unusual facies', 'Weaver like syndrome', 'WVS', 'mental retardation, microcephaly, weight deficiency, unusual facies, clinodactyly, bone hypoplasia, and cleft palate', 'Weaver-Smith syndrome', 'camptodactyly-overgrowth-unusual facies syndrome']",14731,277590,3447,CN036342,"['-0.04767', '-0.0507', '-0.1247', '-0.3584', '0.5806', '-0.9756', '-0.4895', '1.092', '-0.796', '-0.3782', '0.5396', '0.4253', '0.06323', '-0.2096', '-0.1698', '0.1796', '0.5874', '-0.6963', '0.04617', '-0.4692', '0.273', '0.1049', '0.1652', '0.10126', '0.07227', '-0.06647', '0.247', '0.1403', '0.092', '-0.5664', '0.697', '-0.3752', '0.7407', '0.426', '-0.1362', '0.086', '-0.266', '-0.1741', '0.02835', '-0.706', '0.5225', '0.03029', '0.03784', '-0.4004', '0.57', '-0.4102', '-0.1133', '0.04846', '-0.0852', '0.0637', '-0.1926', '-0.1202', '-0.6963', '0.3203', '-0.407', '-0.00634', '-0.4827', '-0.5073', '0.1719', '0.2235', '0.4036', '-0.1466', '-0.5854', '-0.0966', '-0.09064', '0.4807', '0.01587', '-0.182', '-0.04495', '0.7803', '-0.7344', '0.1681', '-0.623', '0.08856', '0.273', '-0.3904', '0.2617', '0.2527', '-0.3027', '-0.4136', '0.1753', '-0.6685', '-0.8135', '0.4004', '-0.2206', '0.9727', '-0.3523', '0.09564', '0.1754', '0.09436', '-0.3088', '-0.1392', '-0.527', '-0.3098', '0.5845', '0.02217', '0.5186', '-0.02959', '1.184', '-0.4482']",C125599,,C536687,759.89,,,
mondo:0010194,Weill-Marchesani syndrome 1,"['Weill-Marchesani syndrome caused by mutation in ADAMTS10', 'Weill-Marchesani syndrome type 1', 'mesodermal Dysmorphodystrophy, congenital', 'ADAMTS10 Weill-Marchesani syndrome', 'Weill-Marchesani syndrome, autosomal recessive', 'Weill-Marchesani syndrome 1', 'Weill-Marchesani syndrome 1, recessive', 'spherophakia-brachymorphia syndrome', 'WMS1']",,277600,,,,,,,,,,
mondo:0010196,Werner syndrome,"['Werner^s syndrome', 'WRN', 'adult progeria', 'adult premature aging syndrome', 'adult premature ageing syndrome', 'Werner syndrome', 'WS']",5688,277700,902,C0043119,"['0.576', '-0.03029', '-0.3901', '0.0914', '0.3237', '-0.1302', '0.3928', '0.815', '0.3696', '-0.7256', '0.02573', '0.2573', '-0.1552', '0.04376', '-0.2462', '0.3994', '0.948', '-0.001327', '-0.7104', '-0.58', '-0.08105', '-0.254', '0.3494', '-0.1722', '0.0674', '0.1716', '-0.0157', '0.3838', '0.1209', '-0.5244', '1.206', '-0.3547', '0.3318', '-0.04172', '-0.0874', '0.505', '0.00934', '-0.4817', '-0.2057', '-0.259', '-0.523', '-0.05197', '0.8105', '0.10016', '0.4497', '0.0146', '0.2146', '0.4182', '0.279', '-0.4324', '0.2573', '-0.012695', '0.231', '0.3284', '0.3606', '0.0741', '0.1082', '-0.5996', '-0.1625', '-0.349', '-0.1038', '-0.2825', '-0.1991', '-0.1718', '-0.2224', '0.89', '0.1868', '1.193', '-0.0731', '0.59', '-0.802', '-0.1606', '0.1959', '0.1365', '0.4873', '-0.3108', '0.05576', '-0.2708', '-0.2559', '-0.8896', '0.331', '-0.4165', '-0.0849', '0.519', '-0.2522', '-0.4402', '0.4849', '-0.04538', '0.552', '-0.268', '-0.1099', '0.1339', '-0.2147', '0.726', '-0.0847', '-0.3455', '0.4194', '-0.1633', '-0.324', '-0.252']",C3447,,D014898,259.8,,10049429,
mondo:0010197,"whistling face syndrome, recessive form","['whistling face syndrome, recessive form']",0111606,277720,,C1848470,,,,C536699,,,,
mondo:0010198,Wernicke-Korsakoff syndrome,"['Korsakoff^s psychosis', 'Korsakov psychosis', 'alcohol-induced encephalopathy', 'Korsakov^s psychosis', 'Wernicke-Korsakoff syndrome', 'Wernicke encephalopathy', 'Korsakoff^s syndrome', 'transketolase defect', 'Korsakoff syndrome']",10915,277730,,,,C35764,1001242,C538669,,,10047913,
mondo:0010199,white forelock with malformations,['white forelock with malformations'],,277740,2475,C1848463,,,,C536700,,,,
mondo:0010200,Wilson disease,"['Westphal pseudosclerosis', 'cerebral pseudosclerosis', 'Westphal-Strumpell syndrome', 'Wilson^s disease', 'hepatolenticular Degeneration', 'Wnd', 'hepatolenticular degeneration', 'Wilson disease', 'WD']",893,277900,905,C0019202,"['-0.11346', '0.3975', '-0.107', '0.4375', '-0.01247', '-0.4167', '-0.5303', '0.3103', '-0.471', '0.0718', '-0.2515', '-0.428', '0.002071', '0.2168', '0.464', '0.01375', '-0.2096', '-0.2783', '0.0104', '-1.217', '-0.372', '-0.616', '0.222', '-0.5366', '-0.252', '-0.1667', '0.1699', '0.407', '0.12177', '-0.646', '0.326', '-0.5747', '0.649', '-0.1709', '-0.1175', '-0.0634', '-0.4158', '0.1105', '0.3823', '-0.158', '0.2502', '-0.0245', '0.2354', '0.1667', '-0.00902', '-0.1696', '-0.4126', '-0.635', '0.0916', '-0.0354', '-0.008446', '0.579', '0.4016', '-0.1783', '0.5234', '0.02077', '-0.11835', '0.4038', '-0.2876', '-0.345', '0.927', '-0.0697', '-0.119', '-0.2812', '-0.2245', '-0.0669', '0.09094', '0.3818', '-0.3628', '-0.1638', '-0.04865', '0.2642', '-0.2196', '0.02455', '0.4111', '-0.02791', '0.4612', '0.1951', '0.199', '-0.0693', '0.1562', '-0.4795', '-0.1236', '-0.259', '0.5024', '0.02948', '0.3445', '-0.1913', '0.7935', '0.1847', '0.219', '0.1581', '-0.7427', '-0.1788', '0.626', '0.4775', '-0.515', '0.256', '0.1826', '-0.2394']",C84756,,D006527,,,10019819,
mondo:0010201,Winchester syndrome,"['NOA syndrome', 'Al-Qeel Sewairi syndrome', 'Torg Winchester syndrome', 'nodulosis arthropathy osteolysis syndrome', 'Winchester-Grossman syndrome', 'multicentric osteolysis, nodulosis and arthropathy', 'WNCHRS', 'Winchester syndrome']",0080696,277950,371428,CN204453,"['-0.1903', '0.0884', '0.1671', '0.006886', '0.08813', '0.00695', '0.003029', '0.2075', '-0.1149', '0.09296', '-0.09314', '-0.003162', '-0.01898', '0.0378', '-0.1138', '-0.1956', '-0.0918', '0.04037', '0.01246', '-0.2578', '0.02551', '-0.1589', '0.0626', '-0.0707', '0.1265', '0.0332', '-0.03586', '-0.02379', '-0.0905', '-0.07306', '0.0055', '-0.08636', '0.0948', '0.1462', '0.03009', '-0.1825', '0.06204', '-0.0445', '0.01709', '-0.3599', '-0.1014', '-0.10956', '0.2319', '-0.1186', '0.08154', '-0.2595', '-0.02852', '0.10205', '0.1755', '0.005962', '-0.02144', '-0.07324', '0.2275', '0.1709', '-0.09875', '-0.1853', '0.04984', '-0.142', '-0.1381', '0.004654', '0.2896', '0.03894', '-0.06775', '-0.05756', '-0.08215', '0.03903', '0.3296', '0.2744', '-0.08734', '0.1981', '-0.06665', '0.02267', '0.0747', '-0.2418', '0.0727', '-0.0663', '-0.015175', '0.1552', '0.0458', '-0.1425', '-0.1937', '0.0387', '-0.02191', '0.2007', '-0.128', '-0.05026', '0.03836', '0.1436', '0.198', '0.002724', '0.06168', '0.0744', '-0.0656', '0.1057', '0.2524', '-0.02396', '0.2194', '-0.3489', '-0.0568', '0.07654']",C170731,,C536709,733.29,,,
mondo:0010203,"intellectual disability, Wolff type","['WOLFF intellectual disability syndrome', 'Wolff-Zimmermann syndrome', 'WOLFF mental retardation syndrome']",,277990,3080,C1848439,,,,C537448,,,,
mondo:0010204,lysosomal acid lipase deficiency,"['cholesterol ester hydrolase deficiency', 'cholesteryl ester storage disease', 'lipa deficiency', 'LAL deficiency', 'Wolman disease', 'lysosomal acid lipase deficiency', 'lysosomal and lipase deficiency']",0080217,278000,275761,,"['-0.4758', '0.2837', '-0.1163', '-0.09106', '0.4492', '-0.10315', '-0.6406', '0.9927', '-0.1527', '-0.0846', '-0.3591', '-0.655', '0.1735', '0.2805', '-0.04163', '-0.9956', '-0.00906', '-0.2847', '-0.3367', '-0.876', '0.002066', '-1.274', '1.086', '0.01627', '-0.2368', '-0.0884', '0.515', '0.10504', '-0.1302', '-0.04584', '0.8184', '-0.3286', '0.824', '0.376', '0.03278', '-0.04175', '-1.003', '-0.010506', '0.1644', '-0.4817', '-0.6104', '-0.481', '0.8784', '-0.03458', '-0.5312', '0.3264', '0.4565', '-0.5723', '-0.8174', '0.08514', '0.1359', '0.2605', '0.1282', '-0.7803', '-0.2211', '0.002026', '-0.01189', '-0.05182', '-0.3477', '0.0492', '0.03192', '0.7227', '0.0768', '-0.584', '0.1252', '0.1516', '0.2019', '-0.099', '-0.2272', '-0.3042', '-0.5996', '-0.2834', '0.253', '0.2133', '-0.08374', '-0.0513', '0.4832', '-0.07086', '-0.4312', '-0.4214', '-0.6343', '-0.3953', '-0.3013', '0.2307', '-0.1461', '0.891', '0.3933', '-0.09296', '0.839', '-0.503', '0.5825', '-0.4224', '-0.1697', '0.0199', '0.607', '0.1665', '0.0644', '0.001064', '0.4277', '-0.812']",,,C531854,,,,
mondo:0010206,hypotrichosis 8,"['hypotrichosis type 8', 'woolly hair, autosomal recessive 1, with or without hypotrichosis', 'LAH3', 'hypotrichosis 8', 'LPAR6 hypotrichosis', 'wooly hair, autosomal recessive 1, with or without hypotrichosis', 'hypotrichosis caused by mutation in LPAR6', 'HYPT8', 'hypotrichosis, localized, autosomal recessive 3']",0110705,278150,,C3279470,,,,C566950,,,,
mondo:0010207,wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome,"['woolly hair, hypotrichosis, everted LOWER LIP, and outstanding ears', 'wooly hair-hypotrichosis-everted lower lip-outstanding ears syndrome', 'woolly hair hypotrichosis everted lower lip and outstanding ears', 'Salamon syndrome', 'wooly hair, hypotrichosis, everted LOWER LIP, and outstanding ears', 'wooly hair hypotrichosis everted lower lip and outstanding ears']",,278200,1409,,,,,C536746,,,,
mondo:0010208,wrinkly skin syndrome,"['wrinkly skin syndrome', 'WSS', 'wrinkled skin syndrome']",0112171,278250,2834,C0406587,"['-0.4197', '-0.041', '0.1423', '-0.2698', '0.7114', '-0.6523', '-0.1306', '0.3777', '-0.7974', '-0.163', '0.1451', '-0.1197', '0.02495', '0.1625', '-0.0826', '0.4192', '0.1472', '0.08826', '-0.1613', '-0.7256', '0.0839', '-0.1222', '0.4353', '-0.3535', '-0.1947', '0.5938', '-0.3442', '0.1693', '0.527', '0.06976', '0.121', '-0.4778', '0.3503', '0.4412', '0.000432', '-0.07117', '-0.432', '-0.2456', '-0.2192', '-0.00821', '0.4043', '-0.9614', '-0.1375', '-0.3577', '0.548', '-0.617', '0.2329', '0.6772', '-0.422', '-0.5635', '-0.251', '-0.05197', '-0.2316', '0.092', '-0.538', '0.2288', '0.2083', '0.254', '-0.1799', '-0.327', '-0.3271', '-0.0693', '-0.789', '0.00426', '0.524', '0.3152', '0.10284', '0.6323', '-0.188', '0.3916', '-0.62', '0.157', '0.2164', '0.2673', '-0.00855', '0.2365', '-0.09595', '-0.6143', '0.2308', '-0.511', '0.3625', '0.1893', '-0.2301', '0.5117', '0.0948', '0.253', '0.181', '0.4646', '0.2432', '-0.1873', '0.5654', '0.369', '0.3586', '0.1813', '-0.0416', '0.3467', '0.12054', '-0.664', '0.645', '0.0445']",,,C536750,259.8,,,
mondo:0010209,xanthinuria type I,"['xanthinuria, type 1', 'xanthine dehydrogenase deficiency', 'XAN1', 'xanthinuria type 1', 'XDH deficiency', 'type 1 xanthinuria', 'xanthine oxidase deficiency', 'xanthine oxidoreductase deficiency', 'xanthinuria, type I', 'XO deficiency', 'XOR deficiency']",,278300,93601,,"['0.03943', '0.05585', '-0.387', '-0.3723', '-0.1814', '-0.2332', '-0.1548', '0.1707', '-0.0914', '0.273', '0.3704', '-0.334', '-0.5845', '0.576', '-0.861', '-0.1776', '0.1503', '0.1394', '0.2712', '-0.2961', '-0.576', '0.1385', '1.033', '-0.3416', '0.02892', '0.1108', '-0.07306', '-0.2021', '0.1287', '-0.1181', '0.04617', '0.126', '0.1456', '0.537', '-0.1683', '-0.776', '-0.88', '-0.176', '-0.3975', '-0.2932', '-0.3813', '-0.3416', '0.4722', '0.2239', '-0.2306', '-0.4863', '0.179', '-0.002506', '-0.0624', '0.3699', '0.4363', '-0.2333', '0.1672', '-0.3135', '-0.4504', '-0.4033', '0.5737', '-0.5093', '-0.619', '0.0777', '0.5894', '-0.2015', '-0.1582', '-0.2299', '-0.0659', '-0.2856', '0.627', '0.7104', '-0.432', '-0.1874', '-0.1838', '-0.2427', '-0.4036', '-0.1655', '0.2131', '0.764', '0.1564', '-0.2542', '0.121', '0.534', '0.03076', '-0.07495', '-0.1032', '0.4482', '0.071', '0.518', '-0.05807', '-0.606', '0.2148', '-0.2195', '0.7295', '0.4756', '-0.0551', '-0.0605', '1.321', '1.018', '0.4048', '-0.1233', '-0.4592', '0.5005']",,,C562584,,,,
mondo:0010210,xeroderma pigmentosum group A,"['XPA', 'xeroderma pigmentosum, group A', 'XPA xeroderma pigmentosum', 'xeroderma pigmentosum 1', 'xeroderma pigmentosum complementation group A', 'XP-A', 'XP1', 'xeroderma pigmentosum, complementation group A', 'XP group A', 'xeroderma pigmentosum, type 1', 'XP, group A', 'xeroderma pigmentosum, complementation group type a', 'xeroderma pigmentosum caused by mutation in XPA', 'xeroderma pigmentosum group type A']",0110843,278700,276249,C0268135,"['-0.0974', '0.2659', '-0.4167', '-0.3745', '0.431', '-0.2289', '-0.01483', '-0.264', '-0.2301', '-0.12286', '0.3813', '0.3389', '-0.0798', '-0.0953', '-0.03265', '-0.1571', '0.1284', '-0.003326', '0.009384', '-0.2888', '-0.3752', '-0.2244', '0.1487', '-0.1843', '0.2224', '0.2296', '0.01558', '0.03662', '0.0413', '0.02777', '0.1604', '-0.02621', '0.2524', '0.1466', '0.1849', '0.00825', '-0.066', '-0.3445', '-0.3098', '-0.4922', '0.3364', '-0.4714', '0.1857', '0.1982', '-0.1265', '-0.448', '-0.01776', '-0.2045', '0.3984', '-0.3188', '0.3337', '-0.4636', '0.0936', '0.244', '-0.02142', '-0.3694', '0.6235', '0.2152', '-0.3838', '-0.02289', '0.3916', '-0.147', '-0.0983', '0.4312', '0.0905', '0.1836', '0.5923', '0.606', '-0.1797', '0.4702', '-0.362', '-0.0886', '0.1633', '0.0495', '0.2305', '-0.3271', '-0.09515', '-0.1499', '0.06525', '-0.3262', '-0.010155', '0.1266', '-0.01093', '0.109', '-0.3826', '-0.4587', '0.3386', '0.4922', '0.1462', '0.138', '0.419', '0.4114', '-0.0818', '-0.01578', '0.3652', '0.192', '0.3994', '-0.452', '0.1349', '0.1532']",C3965,,,,,,
mondo:0010211,xeroderma pigmentosum group C,"['XP3', 'XP, Group C', 'xeroderma pigmentosum, complementation group C', 'XP-C', 'xeroderma pigmentosum, group C', 'XP group C', 'XPCC', 'xeroderma pigmentosum, complementation group type C', 'xeroderma pigmentosum, type 3', 'xeroderma pigmentosum III', 'xeroderma pigmentosum group type C', 'XPC', 'xeroderma pigmentosum 3']",0110844,278720,276255,C2752147,"['0.07886', '0.2219', '-0.4578', '-0.4211', '0.5425', '-0.2113', '-0.1399', '-0.1641', '-0.2051', '-0.121', '0.479', '0.4119', '0.01685', '-0.1414', '-0.1472', '-0.03925', '0.2217', '-0.02174', '-0.01476', '-0.3418', '-0.4307', '-0.4062', '0.1307', '-0.2103', '0.1571', '0.1952', '0.1478', '0.1307', '-0.004776', '0.002066', '0.2041', '0.08264', '0.367', '0.1215', '0.0359', '0.08264', '-0.0265', '-0.3862', '-0.2052', '-0.4365', '0.2847', '-0.4841', '0.2305', '0.166', '-0.1554', '-0.4993', '0.0239', '-0.2174', '0.5854', '-0.2324', '0.1982', '-0.4282', '-0.05368', '0.2238', '-0.014534', '-0.3464', '0.5874', '0.2422', '-0.4578', '-0.066', '0.4727', '-0.0607', '-0.1364', '0.3162', '0.2583', '0.1606', '0.7153', '0.767', '-0.11664', '0.4194', '-0.36', '-0.0738', '0.0751', '0.0776', '0.3762', '-0.308', '-0.1295', '-0.109', '-0.0353', '-0.258', '0.0219', '0.1436', '-0.0814', '0.1495', '-0.4062', '-0.461', '0.3474', '0.406', '0.1763', '0.1743', '0.413', '0.5283', '-0.1414', '0.05463', '0.2268', '0.2389', '0.401', '-0.507', '0.03925', '0.02374']",C114770,,C567886,,,,
mondo:0010212,xeroderma pigmentosum group D,"['XPH', 'xeroderma pigmentosum caused by mutation in ERCC2', 'xeroderma pigmentosum IV', 'ERCC2 xeroderma pigmentosum', 'XP, Group H', 'XP4 xeroderma pigmentosum VIII', 'XP group H', 'XP group D', 'xeroderma pigmentosum 4', 'XP-D', 'xeroderma pigmentosum, group D', 'xeroderma pigmentosum, complementation group D', 'XP8', 'xeroderma pigmentosum, complementation group type D', 'xeroderma pigmentosum VIII', 'XP, Group D', 'xeroderma pigmentosum group type D', 'XP4', 'XP, Group H, formerly', 'XPDC', 'XPD', 'XP4 xeroderma pigmentosum VIII, formerly']",0110845,278730,276258,,"['-0.0928', '0.2452', '-0.3928', '-0.3223', '0.393', '-0.1886', '-0.0364', '-0.289', '-0.2246', '-0.08124', '0.359', '0.3435', '-0.10266', '-0.1559', '-0.04932', '-0.1515', '0.12274', '0.02675', '0.04645', '-0.2314', '-0.3708', '-0.295', '0.07086', '-0.2063', '0.2285', '0.2476', '-0.01473', '-0.002754', '0.03078', '-0.01598', '0.1472', '0.007153', '0.2769', '0.0747', '0.1833', '-0.01022', '-0.05472', '-0.3596', '-0.2305', '-0.4866', '0.3042', '-0.4722', '0.1963', '0.1534', '-0.1475', '-0.422', '0.03006', '-0.1658', '0.3286', '-0.3098', '0.2817', '-0.416', '0.0777', '0.2937', '-0.05988', '-0.3396', '0.6284', '0.2085', '-0.3865', '-0.09344', '0.4116', '-0.0986', '-0.0629', '0.3188', '0.1663', '0.1558', '0.6074', '0.5454', '-0.11365', '0.435', '-0.3674', '-0.02214', '0.2267', '0.01651', '0.1843', '-0.2418', '-0.1169', '-0.1733', '0.02216', '-0.2617', '-0.03244', '0.119', '-0.04984', '0.0841', '-0.3752', '-0.4502', '0.3003', '0.5015', '0.2241', '0.2306', '0.4702', '0.3484', '-0.1185', '-0.01332', '0.311', '0.1864', '0.3972', '-0.4846', '0.05618', '0.1378']",C3967,,C562591,,,,
mondo:0010213,xeroderma pigmentosum group E,"['XP5', 'XP, Group E', 'XPe', 'xeroderma pigmentosum group type E', 'xeroderma pigmentosum, complementation group type E', 'XP-E', 'xeroderma pigmentosum, complementation group E', 'xeroderma pigmentosum, group E, DDB-negative subtype', 'XP group E', 'xeroderma pigmentosum 5', 'xeroderma pigmentosum, type 5', 'xeroderma pigmentosum V', 'XPE']",0110846,278740,276261,C1848411,"['0.1456', '0.1439', '-0.561', '-0.3447', '0.6426', '-0.21', '0.11127', '-0.1555', '-0.11993', '-0.09375', '0.4995', '0.3865', '0.02444', '-0.07477', '0.004555', '-0.09174', '0.2378', '-0.08124', '-0.08466', '-0.3325', '-0.4763', '-0.2412', '0.2272', '-0.1462', '0.344', '0.2181', '0.02388', '0.04553', '0.05917', '-0.1477', '0.422', '0.00732', '0.2966', '0.2048', '0.06995', '0.02043', '-0.1925', '-0.4336', '-0.198', '-0.3542', '0.1443', '-0.6255', '0.1588', '0.02519', '-0.08246', '-0.4243', '0.1385', '-0.1602', '0.5015', '-0.2183', '0.2147', '-0.4905', '-0.0362', '0.2263', '-0.08124', '-0.2399', '0.5103', '0.1957', '-0.3225', '-0.1587', '0.4548', '-0.1071', '-0.04642', '0.335', '0.1074', '0.1954', '0.4521', '0.6587', '0.01727', '0.4382', '-0.3267', '-0.1543', '-0.00869', '0.0486', '0.28', '-0.258', '-0.1576', '-0.1769', '0.0868', '-0.4216', '0.0688', '0.0719', '-0.099', '0.268', '-0.3953', '-0.6104', '0.1525', '0.3584', '0.1893', '0.154', '0.4404', '0.474', '-0.1617', '0.04666', '0.2515', '0.2305', '0.36', '-0.501', '-0.00869', '0.10126']",C114771,,C564732,,,,
mondo:0010214,xeroderma pigmentosum variant type,"['xeroderma pigmentosum variant', 'xeroderma pigmentosum with normal DNA repair rates', 'photosensitivity with defective DNA synthesis', 'XPV', 'xeroderma pigmentosum, variant type']",0110847,278750,90342,C1848410,"['0.1066', '0.3455', '-0.8213', '0.001976', '0.59', '-0.4001', '-0.0632', '0.0782', '-0.08966', '-0.7207', '0.3677', '0.543', '-0.243', '-0.1047', '-0.0744', '-0.642', '0.2825', '-0.562', '-0.309', '-0.2374', '-0.338', '-0.2145', '0.2634', '-0.636', '-0.116', '0.503', '0.1843', '0.05008', '-0.3838', '-0.268', '0.6304', '-0.3071', '0.3247', '0.04715', '0.1588', '0.518', '-0.5195', '-0.499', '-0.3508', '-0.1926', '0.1681', '-0.9634', '-0.1396', '-0.374', '-0.2646', '-0.1477', '-0.1113', '0.002863', '0.8354', '0.03665', '0.58', '-0.0945', '-0.104', '-0.1641', '-0.2566', '-0.3071', '0.2773', '-0.02583', '-0.515', '-0.6367', '0.5923', '-0.0922', '-0.05017', '0.01024', '0.534', '0.5806', '0.3923', '0.1153', '-0.1324', '0.1732', '-0.3022', '-0.07153', '0.1345', '0.2969', '0.5464', '0.206', '-0.154', '-0.2191', '0.10175', '-0.069', '-0.3638', '-0.1302', '0.0753', '0.2708', '0.2927', '-0.542', '0.07117', '0.3513', '0.453', '0.1719', '0.7676', '0.4224', '-0.259', '-0.0955', '0.10986', '0.0806', '0.3643', '-0.6074', '-0.05112', '-0.12213']",C141367,,C536766,,,,
mondo:0010215,xeroderma pigmentosum group F,"['xeroderma pigmentosum, type 6', 'xeroderma pigmentosum group type F', 'xeroderma pigmentosum, complementation group F', 'ERCC4 xeroderma pigmentosum', 'xeroderma pigmentosum caused by mutation in ERCC4', 'xeroderma pigmentosum, group F', 'XP6', 'XP group F', 'XP-F', 'xeroderma pigmentosum, type F/Cockayne syndrome', 'xeroderma pigmentosum, complementation group type F', 'XP, group F', 'xeroderma pigmentosum VI', 'xeroderma pigmentosum 6', 'XPF']",0110848,278760,276264,,"['-0.2126', '0.3535', '-0.0981', '0.154', '0.294', '-0.3171', '0.05145', '-0.1471', '-0.07666', '-0.302', '0.06616', '0.1473', '-0.07684', '0.11414', '-0.1674', '-0.1417', '0.014786', '-0.1589', '-0.03513', '-0.4075', '0.01817', '-0.1256', '0.11725', '-0.05106', '0.000903', '0.1628', '0.02626', '0.12463', '-0.01662', '-0.05533', '0.0643', '0.05667', '0.1036', '0.0646', '0.1681', '-0.01883', '0.0713', '-0.2908', '-0.1656', '-0.4922', '0.108', '-0.5405', '0.1417', '-0.03513', '-0.3296', '-0.561', '0.1646', '-0.06305', '0.4846', '-0.04062', '0.2969', '-0.312', '0.1033', '0.162', '-0.1553', '-0.4482', '0.556', '0.2428', '-0.5195', '-0.1353', '0.1311', '-0.02676', '0.05264', '0.1926', '0.2247', '0.2878', '0.2603', '0.00443', '-0.0845', '0.1105', '-0.564', '-0.01997', '0.2415', '0.07434', '0.2253', '0.1631', '0.0466', '-0.02055', '-0.0627', '-0.1844', '-0.05655', '0.0743', '-0.1477', '0.2039', '0.09546', '-0.1777', '0.3284', '0.395', '0.2817', '0.05615', '0.3816', '0.1371', '-0.02905', '-0.205', '0.2122', '0.276', '0.3054', '-0.494', '0.04462', '0.04724']",C3968,,C562592,,,,
mondo:0010216,xeroderma pigmentosum group G,"['xeroderma pigmentosum, complementation group G', 'XP, Group G', 'XP-G', 'XPG', 'xeroderma pigmentosum, group G/Cockayne syndrome', 'xeroderma pigmentosum group type G', 'xeroderma pigmentosum, group G', 'xeroderma pigmentosum type 7', 'xeroderma pigmentosum complementation group G', 'xeroderma pigmentosum, type G/Cockayne syndrome', 'ERCC5 xeroderma pigmentosum', 'xeroderma pigmentosum caused by mutation in ERCC5', 'xeroderma pigmentosum VII', 'xeroderma pigmentosum, complementation group type G', 'XP7', 'xeroderma pigmentosum 7', 'XP group G']",0110849,278780,276267,C1851443,"['-0.2888', '0.348', '-0.12177', '0.1765', '0.2847', '-0.342', '0.0006113', '-0.2189', '-0.00512', '-0.279', '0.0656', '0.1609', '-0.09564', '0.05228', '-0.1255', '-0.1259', '-0.0511', '-0.0901', '0.04382', '-0.3904', '-0.0274', '-0.11707', '0.0678', '0.03204', '-0.05618', '0.1079', '0.013435', '0.1117', '0.00652', '0.01012', '0.117', '0.0805', '0.1665', '0.08307', '0.182', '0.0001416', '0.165', '-0.3162', '-0.1184', '-0.591', '0.1461', '-0.5234', '0.10626', '0.01143', '-0.3372', '-0.561', '0.1335', '-0.09125', '0.4722', '-0.0485', '0.2915', '-0.2937', '0.1376', '0.21', '-0.07947', '-0.4065', '0.592', '0.2151', '-0.4949', '-0.0988', '0.2147', '-0.03244', '-0.03955', '0.1869', '0.2065', '0.2273', '0.343', '0.05615', '-0.06647', '0.2089', '-0.5713', '-0.02498', '0.2057', '-0.02068', '0.2399', '0.1148', '0.06665', '0.04172', '-0.05603', '-0.129', '-0.00423', '0.0628', '-0.1244', '0.1904', '0.0621', '-0.2218', '0.3435', '0.4124', '0.2405', '0.11096', '0.3713', '0.1729', '-0.01659', '-0.1854', '0.282', '0.2252', '0.293', '-0.4553', '0.01282', '0.0818']",C3969,,C562593,,,,
mondo:0010217,de Sanctis-Cacchione syndrome,"['de Sanctis-Cacchione syndrome', 'xerodermic idiocy']",0112158,278800,1569,CN199649,"['-0.00428', '0.01723', '-0.001026', '-0.01277', '-0.002031', '-0.03284', '0.001817', '0.02364', '-0.028', '-0.00859', '0.001706', '0.000971', '-0.008995', '-0.004566', '-0.01301', '-0.02203', '0.003414', '-0.02808', '-0.004093', '-0.0432', '-0.007427', '-0.00816', '0.01604', '-0.0225', '0.02438', '-0.00915', '-0.01466', '-0.00559', '0.01542', '-0.00482', '0.0139', '-0.00736', '0.02791', '0.02003', '0.002214', '-0.001434', '0.003094', '-0.01593', '-0.005157', '-0.02481', '0.01246', '-0.04382', '0.002256', '-0.0187', '0.01526', '-0.03336', '-0.02267', '0.01118', '0.01554', '0.003883', '-0.01487', '0.001239', '-0.01448', '-0.00838', '-0.0237', '-0.00479', '0.04382', '0.002245', '-0.0316', '-0.003626', '0.014145', '0.00959', '0.002306', '0.006214', '-0.00944', '0.00608', '0.0286', '0.02272', '-0.02617', '0.04105', '-0.03824', '0.00814', '0.007687', '-0.01646', '0.01878', '0.01747', '0.007782', '-0.00806', '-0.01866', '-0.01531', '-0.003063', '-0.00488', '-0.02055', '0.02182', '-0.01584', '0.003073', '0.009995', '0.0343', '0.03053', '0.005836', '0.00798', '0.015335', '0.001129', '0.00416', '0.06177', '0.004257', '0.02968', '-0.04388', '-0.0096', '0.02464']",C84666,,C535992,759.89,,,
mondo:0010218,"46,XX sex reversal 2","['SRXX2', 'chromosome 17Q24 Duplication syndrome', '46,XX SEX reversal 2', '46,XX sex reversal 2', '46,XX Sex reversal type 2', '46XX sex reversal 2']",0111763,278850,,C2749215,,,,,,,,
mondo:0010219,xylosidase deficiency,['xylosidase deficiency'],,278900,,C1848407,,,,C564730,,,,
mondo:0010220,Young syndrome,"['azoospermia, obstructive, and chronic sinopulmonary infections', 'azoospermia-sinopulmonary infections syndrome', 'Barry-Perkins-Young syndrome', 'sinusitis-infertility syndrome', 'azoospermia obstructive and chronic sinopulmonary infections', 'young syndrome', 'Barry Perkins Young syndrome']",,279000,3471,C0340037,,,,C536718,759.89,,10063689,
mondo:0010221,CHIME syndrome,"['CHIME', 'Zunich-Kaye syndrome', 'PIGL-CDG', 'Zunich neuroectodermal syndrome', 'coloboma, congenital heart disease, ichthyosiform dermatosis, mental retardation, and ear anomalies syndrome', 'coloboma, congenital heart disease, ichthyosiform dermatosis, intellectual disability, and ear anomalies syndrome', 'glycosylphosphatidylinositol biosynthesis defect 5', 'neuroectodermal dysplasia, CHIME type', 'coloboma-congenital heart disease-ichthyosiform dermatosis-intellectual disability-ear anomalies syndrome', 'neuroectodermal syndrome, Zunich type', 'congenital disorder of glycosylation due to PIGL deficiency', 'CHIME syndrome']",0112152,280000,3474,C1848392,"['-0.11224', '0.08203', '0.4773', '-0.635', '0.28', '-0.5464', '0.3274', '0.531', '-0.3503', '-0.0637', '-0.2778', '-0.3792', '-0.457', '-0.5024', '-0.543', '0.4397', '0.3765', '-0.333', '-0.02025', '-0.2096', '-0.0679', '0.2195', '-0.327', '-0.075', '0.308', '-0.0261', '-0.778', '0.1016', '0.922', '-0.06186', '0.3347', '0.001813', '-0.08826', '0.4976', '0.07074', '-0.3064', '0.12427', '-0.4683', '-0.3596', '-0.4746', '0.5537', '-0.28', '0.1534', '-0.365', '-0.4966', '-0.2031', '-0.1137', '0.607', '0.05502', '-0.05475', '-0.2173', '-0.1365', '-0.2139', '0.286', '-0.5894', '-0.3877', '0.4377', '-0.03473', '-0.10284', '0.0666', '-0.04688', '0.05707', '-0.5503', '0.07745', '-0.354', '-0.7026', '0.2058', '0.3877', '-0.363', '0.4915', '-0.3457', '0.1361', '0.02142', '-0.1738', '-0.315', '0.6094', '0.541', '-0.4692', '-0.2954', '0.0924', '0.4722', '-0.2898', '0.01117', '0.5503', '0.3606', '0.004475', '0.256', '1.303', '-0.1711', '0.681', '-0.0635', '0.4043', '0.4172', '0.2072', '0.999', '0.10175', '0.6567', '-0.648', '0.2416', '0.3064']",,,C536729,,,,
mondo:0010222,X-linked Opitz G/BBB syndrome,"['X-linked Opitz BBB/G syndrome', 'Opitz Bbbg syndrome, type 1', 'Opitz syndrome', 'telecanthus-hypospadias syndrome', 'Opitz GBBB syndrome, type I, X-linked recessive', 'Opitz GBBB syndrome, type 1', 'Opitz GBBB syndrome, X-linked', 'Opitz syndrome, X-linked', 'Opitz-G syndrome, type 1', 'hypertelorism with esophageal Abnormality and hypospadias', 'hypertelorism-hypospadias syndrome', 'GBBB1', 'XLOS', 'X-linked Opitz syndrome', 'Opitz G/BBB syndrome, X-linked', 'Opitz GBBB syndrome, type I']",,300000,306597,,"['0.05258', '0.3025', '-0.2725', '0.1863', '0.11865', '-0.444', '-0.0875', '0.0922', '-0.3823', '-0.522', '-0.2583', '-0.3423', '0.175', '0.3364', '-0.199', '0.314', '-0.395', '-0.1012', '-0.07794', '-0.2988', '0.144', '0.38', '0.4824', '-0.3428', '0.0681', '-0.1783', '-0.1676', '0.11365', '0.7354', '-0.1042', '0.641', '-0.0817', '0.03464', '0.0479', '0.2856', '-0.0086', '-0.2074', '-0.11566', '-0.528', '-0.212', '0.11633', '-0.3506', '0.2944', '-0.2776', '0.2605', '-0.2764', '-0.172', '0.2717', '-0.3748', '0.3472', '-0.1659', '-0.2769', '-0.3599', '-0.0821', '0.1406', '-0.5854', '0.3826', '0.2866', '0.0543', '0.54', '0.07886', '-0.3784', '0.1963', '0.7217', '-0.189', '-0.1346', '0.09216', '0.2008', '-0.3855', '0.5933', '-0.2925', '0.2026', '0.2455', '0.1771', '-0.004757', '0.2708', '0.3672', '-0.2805', '-0.5093', '-0.156', '0.2021', '-0.084', '-0.134', '0.507', '-0.03015', '0.159', '-0.2052', '0.326', '0.0859', '0.02238', '-0.3608', '0.4385', '0.2058', '0.1084', '0.7446', '-0.12274', '0.2029', '-0.1995', '0.10754', '-0.1036']",,,,,,,
mondo:0010223,"ichthyosis, X-linked, without steroid sulfatase deficiency","['ichthyosis, X-linked, without steroid sulfatase deficiency']",,300001,,C1848387,,,,C564729,,,,
mondo:0010224,corpus callosum agenesis-abnormal genitalia syndrome,"['corpus callosum, agenesis of, with abnormal genitalia', 'Proud syndrome', 'New X-linked syndrome with seizures, acquired micrencephaly, and agenesis of the corpus callosum', 'microcephaly-corpus callosum agenesis-abnormal genitalia syndrome', 'Proud-Levine-Carpenter syndrome', 'ACC-abnormal genitalia syndrome', 'Proud Levine Carpenter syndrome', 'ACC with abnormal genitalia']",0112151,300004,2508,C0796124,"['-0.3882', '0.0567', '0.4182', '-0.8076', '0.12396', '-0.8096', '-0.0862', '0.841', '-0.4688', '-0.3748', '-0.1594', '-0.3684', '-0.1266', '-0.1274', '-0.2532', '-0.0966', '0.3533', '-0.207', '-0.3892', '-0.3376', '0.3967', '0.1964', '0.3083', '-0.1061', '-0.04132', '-0.1519', '-0.06726', '0.1027', '0.535', '-0.464', '0.1866', '-0.5933', '0.8755', '-0.12085', '0.1355', '-0.1357', '-0.00621', '-0.5713', '-0.357', '-0.1426', '0.619', '-0.1279', '-0.2832', '0.1467', '-0.2524', '-0.565', '-0.1686', '0.3792', '-0.3047', '-0.11346', '-0.2213', '0.1963', '-0.1316', '-0.08673', '-0.439', '0.1416', '0.1065', '-0.258', '-0.11804', '0.03854', '-0.2002', '-0.1505', '-0.0467', '0.4734', '-0.612', '0.1346', '0.2432', '0.5356', '-0.4043', '0.3613', '-0.07904', '0.1985', '0.2844', '0.143', '-0.127', '0.1376', '0.3271', '-0.3135', '-0.6123', '-0.2444', '0.1823', '0.3835', '0.2443', '0.4443', '-0.03976', '0.1764', '-0.1067', '0.2213', '0.2417', '-0.004715', '0.2164', '0.4355', '0.3025', '0.2167', '0.6245', '-0.05896', '0.6553', '-0.0644', '0.4983', '0.4426']",,,C563110,,,,
mondo:0010225,Dent disease type 1,"['Dent disease caused by mutation in CLCN5', 'DENT disease 1', 'nephrolithiasis 2', 'dent disease 1, X-linked recessive', 'Dent disease type 1', 'CLCN5 Dent disease', 'nephrolithiasis, hypercalciuric, X-linked', 'nephrolithiasis type 1', 'urolithiasis, hypercalciuric, X-linked']",0111798,300009,93622,CN206679,,,,,,,,
mondo:0010226,"46,XY sex reversal 2","['46,XY sex reversal 2', '46XY sex reversal 2, dosage-sensitive', '46,XY SEX reversal 2', '46,XY Sex reversal type 2', '46,XY Sex reversal, Dax1-related', 'dosage-sensitive Sex reversal', 'SRXY2']",0111777,300018,,C1848296,,,,C535601,,,,
mondo:0010227,retinitis pigmentosa 3,"['RP3', 'retinitis pigmentosa type 3', 'retinitis pigmentosa caused by mutation in RPGR', 'cone-rod Degeneration, X-linked', 'RPGR retinitis pigmentosa', 'retinitis pigmentosa 3', 'retinitis pigmentosa 15', 'Choroidoretinal Degeneration with retinal reflex in heterozygous Women']",0110414,300029,,C1845667,,,,C564520,,H35.5,,
mondo:0010228,"hearing loss, X-linked 3","['deafness, X-linked 4, congenital sensorineural', 'deafness, X-linked 3', 'deafness X-linked, DFN3', 'DFNX3']",0111736,300030,,,,,,C564727,,,,
mondo:0010229,"alopecia, congenital","['ALPC', 'alopecia, congenital', 'congenital alopecia']",,300042,,,,C35790,,C535981,,,,
mondo:0010230,"intellectual disability, X-linked 23","['mental retardation, X-linked 23', 'MRX23', 'intellectual disability, X-linked 23']",0112049,300046,,C0796229,,,,C563144,,,,
mondo:0010231,"intellectual disability, X-linked 20","['mental retardation, X-linked 20', 'MRX20', 'intellectual disability, X-linked 20']",0112023,300047,,C0796226,,,,C563142,,,,
mondo:0010232,"intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked","['congenital short bowel syndrome, X-linked', 'intestinal pseudoobstruction, neuronal, chronic idiopathic, X-linked', 'intestinal pseudoobstruction neuronal chronic idiopathic X-linked', 'Ciip, X-linked', 'intestinal pseudoobstruction, neuronal, X-linked recessive', 'CIIP X-linked', 'congenital idiopathic intestinal pseudoobstruction', 'CIIP', 'intestinal pseudoobstruction, neuronal, chronic idiopathic, with central nervous system involvement', 'Ipox', 'congenital short bowel syndrome, X-linked recessive', 'CIIPX']",0080681,300048,,,,,,C535532,,,,
mondo:0010233,"heterotopia, periventricular, X-linked dominant","['PVNH1', 'nodular heterotopia, bilateral periventricular', 'BPNH', 'NHBP', 'heterotopia, periventricular, 1, X-linked dominant', 'bilateral periventricular nodular heterotopia', 'heterotopia periventricular X-linked dominant', 'nodular heterotopia bilateral periventricular', 'periventricular nodular heterotopia 1', 'heterotopia, periventricular, Ehlers-Danlos variant', 'heterotopia familial nodular', 'heterotopia, familial nodular', 'periventricular nodular heterotopia 4', 'X-linked periventricular heterotopia', 'heterotopia, periventricular nodular, with Frontometaphyseal dysplasia', 'heterotopia, periventricular, X-linked dominant', 'periventricular nodular heterotopia 4, formerly']",,300049,,,,,,,742.4,,,
mondo:0010235,X-linked intellectual disability-psychosis-macroorchidism syndrome,"['X-linked mental retardation with spasticity', 'intellectual deficit, X-linked - psychosis - macroorchidism', 'mental retardation, X-linked, syndromic 13', 'MRXS13', 'X-linked intellectual disability 79', 'intellectual disability, X-linked 79', 'mental retardation with psychosis, pyramidal signs, and macroorchidism', 'intellectual disability, X-linked 16', 'intellectual disability, X-linked, with spasticity', 'X-linked intellectual disability with spasticity', 'mental retardation psychosis macroorchidism', 'mental retardation, X-linked, syndromic type 13', 'intellectual disability with psychosis, pyramidal signs, and macroorchidism', 'intellectual developmental disorder, X-linked, syndromic 13, X-linked recessive', 'mental retardation, X-linked, with spasticity', 'PPM-X syndrome', 'intellectual disability, X-linked, syndromic 13', 'intellectual disability psychosis macroorchidism', 'mental retardation, X-linked 79', 'X-linked mental retardation 79', 'PPM-X', 'intellectual disability, X-linked, syndromic type 13', 'mental retardation, X-linked 16', 'Lindsay-Burn syndrome']",0060827,300055,3077,,"['-0.2988', '0.3074', '0.3232', '-0.6294', '-0.1791', '-0.5034', '0.07086', '0.56', '-0.4993', '-0.3801', '-0.2725', '-0.1205', '0.1169', '0.07336', '0.3206', '0.2163', '0.2041', '-0.0985', '-0.462', '-0.5205', '-0.09973', '0.0365', '-0.03029', '-0.2131', '0.3555', '-0.217', '-0.0789', '-0.2089', '0.04865', '-0.1979', '0.2277', '-0.0353', '0.677', '0.0632', '-0.0536', '-0.1598', '-0.368', '-0.3608', '-0.3125', '-0.1638', '0.3462', '-0.1729', '-0.3079', '0.0862', '0.137', '-0.4495', '0.0473', '-0.09955', '-0.319', '0.11664', '-0.3254', '0.196', '-0.4795', '-0.1925', '0.1597', '0.2874', '0.2615', '-0.3604', '-0.1284', '0.221', '0.02007', '0.009575', '0.06635', '0.3523', '-0.2927', '0.0623', '-0.03372', '0.4604', '-0.1636', '0.1813', '-0.481', '0.1242', '-0.1504', '-0.2986', '0.094', '-0.0811', '0.3716', '-0.2085', '-0.153', '-0.08905', '0.1309', '-0.2468', '-0.0975', '0.4312', '0.363', '0.4326', '-0.1105', '0.0901', '0.422', '0.2727', '0.1965', '0.6045', '-0.00818', '0.313', '0.5337', '0.271', '0.02977', '-0.1783', '0.5825', '0.337']",,,,758.89,,,
mondo:0010236,"intellectual disability, X-linked 14","['MRX14', 'mental retardation, X-linked 14', 'mental retardation, X-linked nonspecific, type 14', 'intellectual disability, X-linked nonspecific, type 14', 'intellectual disability, X-linked 14']",0112027,300062,,,,,,C537454,,,,
mondo:0010237,X-linked intellectual disability-plagiocephaly syndrome,"['intellectual disability, X-linked, with craniofacial dysmorphism', 'Hyde Forster McCarthy Berry syndrome', 'intellectual disability, X-linked Hyde-Forster type', 'mental retardation, plagiocephaly, brachycephaly, prominent forehead, and coarse facial features', 'mental retardation, X-linked, Hyde-Forster type', 'Hyde Forster-McCarthy-Berry syndrome', 'plagiocephaly and X-linked mental retardation', 'mental retardation, X-linked Hyde-Forster type', 'intellectual disability, plagiocephaly, brachycephaly, prominent forehead, and coarse facial features', 'mental retardation, X-linked, with craniofacial dysmorphism', 'plagiocephaly and X-linked intellectual disability', 'intellectual disability, X-linked, Hyde-Forster type']",,300064,2898,C2931516,,,,C537512,,,,
mondo:0010238,"hearing loss, X-linked 4","['X-linked nonsyndromic deafness caused by mutation in SMPX', 'DFNX4', 'deafness, X-linked 6, progressive', 'deafness, X-linked type 4', 'SMPX X-linked nonsyndromic deafness', 'deafness, X-linked 4, X-linked dominant', 'deafness, X-linked 4', 'deafness, nonsyndromic sensorineural progressive 6']",0111735,300066,,C1848204,,,,C564723,,,,
mondo:0010239,lissencephaly type 1 due to doublecortin gene mutation,"['lissencephaly, X-linked', 'X-linked lissencephaly', 'subcortical band heterotopia, X-linked', 'subcortical laminar heterotopia, X-linked', 'lissencephaly, X-linked, 1', 'lissencephaly, X-linked, type 1', 'Xlis', 'lissencephaly X-linked', 'lissencephaly and agenesis of corpus callosum', 'X-linked lissencephaly type 1', 'subcortical laminar heterotopia, X-linked,', 'subcortical laminal heterotopia, X-linked', 'Double cortex syndrome', 'LISX1', 'Dc syndrome', 'LISX', 'XLIS']",0112239,300067,2148,C4275012,"['0.2043', '-0.1111', '0.503', '-0.2412', '0.05374', '-0.525', '0.2773', '0.2883', '-0.7637', '-0.688', '-0.415', '-0.334', '0.04178', '0.302', '0.4395', '-0.1271', '0.2114', '-0.4216', '-0.1036', '-0.3506', '-0.2029', '-0.0347', '0.3474', '0.0821', '-0.2158', '-0.246', '0.3862', '-0.07446', '-0.098', '0.003054', '0.3323', '0.10565', '0.382', '0.601', '-0.4072', '-0.10986', '-0.006176', '-0.3682', '0.07855', '-0.382', '0.55', '-0.3364', '-0.173', '0.502', '-0.1974', '0.1237', '0.0949', '-0.4336', '-0.0453', '0.3462', '0.1016', '0.05627', '0.0819', '0.05545', '0.07007', '0.391', '0.1274', '-0.125', '-0.1197', '0.319', '0.1267', '0.1964', '0.3079', '-0.0385', '-0.06433', '0.247', '0.4958', '0.1301', '-0.1864', '0.2551', '-0.2485', '-0.1033', '0.2798', '0.02063', '0.3157', '0.1953', '0.4387', '-0.3044', '-0.512', '-0.07635', '-0.2098', '0.4873', '-0.072', '0.1635', '-0.07367', '0.3625', '-0.04138', '0.0855', '0.5015', '0.1313', '-0.215', '0.3223', '0.10345', '0.05164', '-0.1711', '0.3389', '0.5747', '-0.09216', '0.3257', '0.3066']",,,,,,,
mondo:0010241,congenital stationary night blindness 2A,"['CSNB, incomplete, X-linked', 'congenital stationary night blindness type 2A', 'CSNB2A', 'night blindness, congenital stationary, type 2', 'congenital stationary night blindness caused by mutation in CACNA1F', 'night blindness, congenital stationary (incomplete), 2A, X-linked', 'night blindness, congenital stationary, type 2A', 'CACNA1F congenital stationary night blindness', 'congenital stationary night blindness 2A X-linked']",0110871,300071,,C1848172,,,,,,,,
mondo:0010242,"fetal akinesia syndrome, X-linked","['fetal akinesia syndrome X-linked', 'X-linked form of foetal akinesia syndrome', 'X-linked form of fetal akinesia syndrome', 'fetal akinesia syndrome, X-linked', 'foetal akinesia syndrome X-linked', 'polyhydramnios, hypokinesia, brain malformations, telecanthus, and narrow palpebral fissures']",0081043,300073,,C1848171,,,,C537921,,,,
mondo:0010243,X-linked immunoneurologic disorder,"['Woods-Black-Norbury syndrome', 'Woods-Black-Norbury syndrome, X-linked dominant', 'immunoneurologic disorder, X-linked', 'neonatal death immune deficiency', 'X-linked immunoneurological disorder', 'Woods Black Norbury syndrome']",,300076,2571,C1848144,,,,C536743,,,,
mondo:0010244,CGF1,"['cognitive function 1, social', 'CGF1', 'social cognition']",,300082,,C1848140,,,,,,,,
mondo:0010245,X-linked cone-rod dystrophy 2,"['X-linked cone dystrophy 2', 'cone dystrophy X-linked 2', 'cone-rod dystrophy X-linked 2', 'cone-rod dystrophy, X-linked, 2', 'cone dystrophy 2, X-linked', 'cone dystrophy, progressive X-linked, 2', 'COD2', 'CORDX2', 'X-linked cone-rod dystrophy type 2']",0111006,300085,1871,,,,,C564717,,,,
mondo:0010246,"developmental and epileptic encephalopathy, 9","['epilepsy, female restricted, with mental retardation', 'early infantile epileptic encephalopathy caused by mutation in PCDH19', 'PCDH19-related FLE', 'epilepsy, female-restricted, with mental retardation', 'early infantile epileptic encephalopathy 9', 'female restricted epilepsy with mental retardation', 'early infantile female-limited epilecptic encephalopathy', 'early infantile epileptic encephalopathy type 9', 'familial epilepsy and intellectual disability limited to females', 'Juberg-Hellman syndrome', 'PCDH19-related infantile epileptic encephalopathy', 'DEE9', 'female restricted epilepsy with intellectual disability', 'PCDH19-related female-limited epilepsy', 'epilepsy and mental retardation limited to females', 'epilepsy, female restricted, with intellectual disability', 'epilepsy, female-restricted, with intellectual disability', 'EIEE9', 'epileptic encephalopathy, early infantile, 9', 'epilepsy and intellectual disability limited to females', 'PCDH19 early infantile epileptic encephalopathy', 'developmental and epileptic encephalopathy 9', 'EFMR', 'familial epilepsy and mental retardation limited to females', 'epileptic encephalopathy, early infantile, type 9', 'female restricted epilepsy with intellectual deficit', 'Juberg Hellman syndrome']",0060848,300088,101039,C1848137,"['0.181', '0.4656', '-0.107', '-0.3994', '0.04108', '-0.5317', '0.384', '0.6685', '-0.3618', '-0.3384', '-0.279', '0.05518', '-0.0413', '0.0997', '0.336', '-0.1888', '0.05893', '-0.04926', '-0.207', '-0.4297', '-0.04147', '0.02594', '-0.0242', '-0.1063', '0.2932', '-0.2421', '-0.354', '-0.276', '0.13', '-0.0692', '0.3364', '-0.2388', '0.4521', '0.0772', '0.0837', '-0.0052', '-0.1575', '-0.4285', '-0.3665', '0.06247', '0.374', '-0.5283', '-0.2163', '-0.1236', '0.223', '-0.2325', '-0.3362', '-0.04984', '-0.2035', '0.888', '-0.2152', '0.1953', '-0.0328', '-0.303', '0.1423', '0.3765', '0.2222', '-0.2983', '0.1315', '0.445', '-0.04654', '-0.02347', '0.4875', '0.2289', '-0.1', '0.2542', '0.1621', '0.2722', '-0.11816', '0.2141', '-0.0386', '0.1239', '-0.1951', '0.118', '-0.001445', '0.08685', '0.1799', '-0.2625', '-0.155', '-0.2566', '0.0884', '0.2627', '0.2678', '0.1788', '0.1826', '0.07074', '-0.1294', '-0.02893', '0.3708', '0.3206', '-0.2189', '0.571', '0.185', '-0.01236', '0.2832', '0.2008', '0.1929', '-0.415', '0.3445', '-0.1265']",,,C564715,,,,
mondo:0010247,X-linked cerebral adrenoleukodystrophy,"['Siemerling-Creutzfeldt disease', 'melanodermic leukodystrophy', 'adrenomyeloneuropathy', 'Addison disease and cerebral sclerosis', 'bronze Schilder disease', 'X-linked cerebral adrenoleukodystrophy', 'ALD', 'adrenoleukodystrophy', 'childhood cerebral ALD', 'ALD childhood cerebral form', 'adrenoleukodystrophy X-linked cerebral form', 'childhood-onset cerebral X-linked adrenoleukodystrophy', 'adrenoleukodystrophy childhood cerebral form']",,,139396,CN199389,"['0.02263', '0.2338', '-0.1652', '-0.1932', '-0.3838', '0.3894', '0.0609', '0.439', '-0.3176', '-0.548', '0.1976', '-0.2069', '0.2172', '0.2632', '0.4675', '-1.107', '-0.2998', '0.2944', '-0.2499', '-0.56', '-0.1532', '-0.11194', '0.1208', '-0.46', '-0.1327', '-0.3625', '-0.1228', '-0.02737', '-0.1506', '-0.2917', '0.1923', '0.2893', '0.9043', '-0.0193', '-0.1724', '0.2355', '-0.4888', '-0.4521', '-0.5864', '-0.3833', '0.2268', '-0.35', '0.1382', '-0.4966', '-0.1519', '-0.1404', '-0.4185', '-0.8677', '-0.2717', '0.5864', '0.899', '0.09863', '-0.2024', '-0.2113', '0.0803', '-0.06635', '0.868', '-0.122', '-0.158', '0.4167', '0.0377', '0.165', '0.3984', '0.2318', '-0.2312', '0.09106', '0.4995', '-0.2812', '-0.3235', '0.251', '0.0583', '0.1139', '-0.3054', '-0.1105', '0.2954', '0.08655', '-0.0747', '-0.3032', '-0.772', '-0.318', '-0.2788', '-0.509', '-0.2274', '-0.2205', '-0.2184', '0.461', '-0.03577', '-0.2004', '0.8013', '0.06476', '0.5044', '0.505', '-0.0651', '0.1409', '0.2688', '0.0848', '-0.1921', '0.3167', '-0.0549', '0.439']",,,,,,,
mondo:0010248,X-linked spondyloepimetaphyseal dysplasia,"['spondyloepimetaphyseal dysplasia, X-linked', 'SEMD, X-linked', 'spondylo-epimetaphyseal dysplasia', 'spondyloepimetaphyseal dysplasia, X-linked, X-linked recessive', 'SEMD X-linked', 'SEMDX', 'spondyloepimetaphyseal dysplasia X-linked']",0112150,300106,93349,C1848097,"['-0.9653', '0.0817', '0.264', '-0.4753', '0.1632', '-0.1915', '-0.02774', '0.632', '-0.8115', '-0.1761', '0.1299', '0.1548', '-0.03677', '0.00959', '0.04736', '0.1052', '0.407', '0.0547', '-0.3413', '-0.7515', '-0.10693', '0.1166', '0.532', '-0.1301', '-0.11523', '0.01868', '0.158', '-0.4636', '0.1066', '-0.3484', '0.238', '-0.3228', '0.342', '0.1565', '0.321', '-0.001357', '-0.11835', '-0.599', '-0.01257', '-0.6885', '0.0753', '-0.5513', '-0.12103', '-0.06573', '-0.434', '-0.4563', '-0.2744', '0.519', '0.2764', '-0.04718', '0.2135', '0.2123', '-0.1316', '0.3235', '-0.3496', '-0.806', '-0.1216', '-0.51', '0.0887', '-0.116', '0.4507', '0.01791', '-0.7666', '-0.03812', '-0.4111', '0.11206', '0.212', '0.423', '-0.3438', '0.1123', '-0.3752', '0.05563', '0.2593', '-0.3381', '-0.2505', '0.2126', '-0.5107', '0.175', '-0.1771', '-0.2438', '-0.2203', '0.01538', '0.1602', '0.5337', '-0.1838', '0.2854', '-0.2815', '0.01602', '0.358', '-0.10266', '-0.3728', '0.07294', '-0.09766', '0.599', '0.7915', '0.0794', '0.54', '-0.2783', '0.4514', '0.4888']",,,C564714,,,,
mondo:0010250,"intellectual disability, X-linked 49","['mental retardation, X-linked 15', 'intellectual disability, X-linked 15', 'intellectual disability, X-linked 49', 'Raynaud-Claes syndrome, X-linked dominant', 'MRX49', 'mental retardation, X-linked 49', 'CLCN4-related X-linked intellectual disability syndrome']",0112060,300114,485350,,,,,,,,,
mondo:0010251,"intellectual disability, X-linked 50","['intellectual disability, X-linked 50', 'intellectual developmental disorder, X-linked 50', 'MRX50', 'mental retardation, X-linked 50']",0112029,300115,,C1848087,,,,C564713,,,,
mondo:0010252,"intellectual disability, X-linked, with panhypopituitarism","['intellectual disability, X-linked, with panhypopituitarism', 'mental retardation, X-linked, with panhypopituitarism', 'intellectual developmental disorder, X-linked, with isolated growth hormone deficiency', 'intellectual disability, X-linked, with isolated Growth hormone deficiency', 'mental retardation, X-linked, with isolated Growth hormone deficiency']",,300123,67045,C1848068,"['-0.3901', '0.1488', '-0.2451', '-0.2786', '0.0674', '0.267', '0.3955', '-0.0849', '-0.0873', '-0.3489', '0.04538', '-0.1504', '0.1104', '0.231', '-0.3032', '-0.2542', '-0.01901', '-0.012985', '-0.2908', '-0.442', '-0.0967', '-0.1824', '0.2233', '-0.4702', '0.2108', '-0.187', '-0.07623', '-0.08887', '0.11615', '-0.2786', '0.1654', '-0.04498', '0.3452', '-0.163', '0.006413', '-0.1863', '-0.02837', '-0.1298', '-0.1252', '-0.2118', '0.10846', '0.2335', '-0.0423', '-0.2708', '0.2898', '-0.275', '0.2078', '-0.2144', '0.0817', '-0.06097', '0.09375', '0.04178', '0.09015', '0.1871', '-0.1992', '0.2117', '0.4192', '-0.13', '-0.2328', '0.2474', '0.08405', '0.1372', '-0.1847', '0.09406', '-0.1603', '0.3225', '0.3447', '0.4404', '-0.363', '-0.08887', '-0.2369', '0.1459', '0.3933', '-0.2313', '-0.07916', '0.1959', '0.2499', '0.04376', '-0.0583', '-0.08606', '-0.2158', '0.4436', '-0.1581', '0.08984', '-0.0818', '-0.1394', '0.316', '-0.07526', '0.3247', '0.146', '0.1749', '0.0696', '-0.0178', '-0.3435', '0.817', '-0.0857', '0.1843', '-0.2764', '-0.01499', '0.3684']",,,,,,,
mondo:0010253,"migraine, familial typical, susceptibility to, 2","['migraine, familial typical, susceptibility to, 2', 'Mfts', 'migraine with or without aura, susceptibility to, 2', 'migraine, familial typical, susceptibility to, type 2', 'Mgr2']",,300125,,,,,,,,,,
mondo:0010255,"diabetes mellitus, insulin-dependent, X-linked, susceptibility to","['diabetes mellitus, insulin-dependent, X-linked', 'insulin-dependent diabetes mellitus, X-linked, susceptibility to', 'diabetes mellitus, insulin-dependent, X-linked, susceptibility to', 'Iddmx']",,300136,,C1848042,,,,,,,,
mondo:0010256,"intellectual disability, X-linked 21","['intellectual developmental disorder, X-linked 21, X-linked recessive', 'mental retardation, X-linked 21', 'intellectual disability, X-linked 34', 'intellectual disability, X-linked type 21', 'mental retardation, X-linked type 21', 'mental retardation, X-linked 34', 'MRX21', 'intellectual disability, X-linked 21', 'IL1RAPL1 non-syndromic X-linked intellectual disability', 'non-syndromic X-linked intellectual disability caused by mutation in IL1RAPL1']",0112022,300143,,,,,,,,,,
mondo:0010257,"prostate cancer, hereditary, X-linked 1","['prostate cancer, hereditary, X-linked 1', 'HPCX1', 'prostate cancer susceptibility, X-linked']",,300147,,C1846279,,,,,,,,
mondo:0010258,MEHMO syndrome,"['intellectual disability, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity', 'MRXS25', 'MEHMO', 'intellectual disability, X-linked, syndromic, Borck type', 'X-linked intellectual disability-epileptic seizures-hypogenitalism-microcephaly-obesity syndrome', 'mental retardation, X-linked, syndromic 20', 'intellectual disability, X-linked, syndromic 25', 'syndromic X-linked mental retardation 20', 'intellectual disability, X-linked, syndromic 20', 'X-linked MEHMO syndrome', 'MEHMO syndrome', 'MRXSBRK', 'mental retardation, X-linked, syndromic 25', 'syndromic X-linked mental retardation 25', 'MRXS20', 'mental retardation, X-linked, syndromic, Borck type', 'MEHMO syndrome, X-linked recessive', 'syndromic X-linked intellectual disability 20', 'syndromic X-linked intellectual disability 25', 'mental retardation, epileptic seizures, hypogonadism and hypogenitalism, microcephaly, and obesity']",0060801,300987,85282,C4310813,"['-0.3591', '0.936', '0.06586', '-0.2715', '0.458', '-0.828', '0.3706', '1.057', '-0.6763', '-0.656', '-0.214', '0.02965', '0.765', '0.0932', '-0.1455', '-0.9155', '0.1257', '0.06964', '-0.727', '-0.5903', '0.48', '0.3083', '0.566', '-0.641', '0.06476', '0.05164', '-0.3665', '-0.4082', '0.0616', '-0.518', '0.997', '-0.4634', '0.6006', '0.1119', '-0.0424', '-0.3694', '-0.576', '0.2505', '-1.028', '0.1339', '0.2345', '-0.01073', '-0.0448', '-0.0936', '0.193', '0.03052', '-0.256', '-0.576', '-0.9995', '-0.781', '-0.005283', '0.11005', '-0.447', '0.1477', '0.3394', '0.2515', '0.9585', '0.1458', '0.4197', '0.6006', '-0.01283', '0.3179', '0.2261', '0.3716', '-0.4558', '0.395', '-0.244', '0.11285', '-0.5767', '-0.0725', '0.01913', '-0.196', '0.1748', '0.6396', '-0.10706', '-0.1478', '0.2725', '0.1968', '-0.598', '0.8564', '0.2905', '0.544', '-0.506', '0.4822', '-0.0749', '0.6807', '0.12286', '0.562', '0.47', '0.3604', '0.524', '0.747', '-0.2059', '-0.3616', '1.006', '-0.05444', '-0.2688', '-0.736', '0.0709', '-0.07227']",,,C537451,,,,
mondo:0010259,retinitis pigmentosa 24,"['RP24', 'retinitis pigmentosa 24', 'RP 24', 'retinitis pigmentosa type 24']",0110416,300155,,C3887982,,,,,,H35.5,,
mondo:0010260,"arthrogryposis, congenital, lower limb, X-linked","['arthrogryposis, congenital, LOWER limb, X-linked', 'ACLLX', 'arthrogryposis, X-linked, type V, formerly', 'arthrogryposis, X-linked, type V']",,300158,,C1846273,,,,C564574,,,,
mondo:0010261,"microphthalmia, syndromic 2","['MAA2 (formerly)', 'microphthalmia, syndromic 2, X-linked dominant', 'microphthalmia, syndromic type 2', 'syndromic microphthalmia type 2', 'microphthalmia, syndromic 2', 'OFCD syndrome', 'oculofaciocardiodental syndrome', 'cataract-microphthalmia-radiculomegaly-cardiac septal defect syndrome', 'ANOP2 (formerly)', 'microphthalmia syndromic 2', 'microphthalmia cataracts radiculomegaly and septal heart defects', 'MCOPS2', 'microphthalmia, cataracts, radiculomegaly, and septal heart defects']",0111809,300166,568,,"['-0.1823', '-0.4285', '0.2825', '-0.2064', '0.07385', '-0.1451', '0.2524', '1.256', '-0.2693', '-0.2335', '-0.6733', '-0.553', '0.0904', '0.1776', '-0.7754', '0.0665', '0.1404', '-0.4646', '-0.2416', '-0.524', '-0.1818', '0.02509', '-0.10156', '0.001966', '0.171', '-0.2778', '-0.4314', '0.1825', '0.8115', '-0.1753', '0.301', '0.3096', '-0.1831', '0.2593', '0.2854', '-0.2028', '0.4514', '-0.4717', '0.251', '-0.394', '0.00391', '-0.09283', '0.6387', '-0.3223', '0.11395', '0.10034', '-0.05823', '0.717', '-0.545', '-0.0994', '0.2214', '0.547', '0.0403', '-0.1121', '-0.754', '-0.5444', '0.117', '-0.13', '0.1919', '-0.02074', '0.47', '0.0789', '-0.1769', '0.0496', '-0.11884', '-0.06018', '0.3445', '0.9883', '-0.2708', '0.2517', '-0.2834', '0.417', '0.1746', '-0.3262', '-0.004364', '0.1605', '0.0663', '-0.646', '-0.1438', '0.546', '0.1298', '-0.1404', '-0.266', '0.5195', '-0.07434', '-0.09045', '-0.2842', '0.01478', '-0.015076', '-0.1365', '-0.304', '0.1764', '0.3494', '0.6904', '0.995', '-0.0473', '0.754', '-0.611', '0.3372', '0.268']",,,,759.89,,,
mondo:0010262,"hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses","['hypotonia, congenital nystagmus, ataxia, and abnormal auditory brainstem responses', 'hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem response']",,300184,,C1970936,,,,C537159,,,,
mondo:0010263,Alport syndrome-intellectual disability-midface hypoplasia-elliptocytosis syndrome,"['AMME complex', 'AMME syndrome', 'Alport syndrome, intellectual disability, midface hypoplasia, and elliptocytosis', 'Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis', 'ATS-MR', 'chromosome Xq22.3 telomeric deletion syndrome', 'Ats-Mr']",0111860,300194,86818,C1846242,"['-0.002062', '0.2228', '0.08844', '-0.2034', '0.2688', '-0.625', '-0.1187', '0.252', '0.002197', '-0.6245', '0.1031', '-0.429', '0.0543', '-0.4438', '0.04285', '0.1362', '-0.0304', '-0.1054', '-0.3628', '-0.552', '0.02116', '0.1729', '0.10986', '-0.4749', '0.3955', '-0.12286', '-0.10693', '-0.1279', '0.3857', '-0.1995', '0.12036', '-0.1849', '0.2418', '0.0957', '0.2356', '-0.341', '-0.12067', '-0.4175', '-0.226', '-0.4888', '-0.06537', '-0.3037', '0.079', '-0.4568', '-0.0286', '-0.4202', '0.0696', '-0.05212', '-0.05673', '-0.625', '-0.2996', '-0.196', '0.10565', '0.2318', '0.1665', '-0.3708', '0.3413', '0.165', '-0.566', '0.3384', '-0.09875', '-0.2495', '0.07446', '0.2482', '-0.1572', '-0.2207', '-0.0642', '0.365', '-0.4546', '0.3123', '-0.3865', '-0.0833', '0.147', '0.1095', '-0.2095', '0.1897', '0.2417', '0.1691', '-0.406', '0.2754', '0.1992', '0.2568', '-0.05103', '0.6235', '0.227', '0.1736', '0.1616', '0.6636', '-0.0911', '0.04938', '0.0921', '0.4832', '0.2345', '-0.4019', '0.9185', '0.2666', '0.1681', '-0.7324', '0.3833', '0.001492']",,,C564570,,,,
mondo:0010264,X-linked adrenal hypoplasia congenita,"['AHC with isolated gonadotropin deficiency', 'X-linked AHC', 'cytomegalic adrenocortical hypoplasia', 'adrenal hypoplasia, congenital', 'adrenal hypoplasia, congenital, with hypogonadotropic hypogonadism', 'AHC with HHG', 'Addison disease, X-linked', 'mineralocorticoid deficiency, isolated', 'X-linked congenital adrenal hypoplasia', 'adrenal insufficiency, progressive, and hypogonadotropic hypogonadism', 'adrenal hypoplasia, congenital, X-linked recessive', 'adrenal hypoplasia congenita', 'congenital adrenal hypoplasia', 'cytomegalic congenital adrenal hypoplasia', 'adrenal hypoplasia, congenital, with precocious puberty', 'AHC']",0080156,300200,95702,C0342482,"['-0.7534', '0.2101', '0.04865', '-0.561', '0.02832', '-0.10516', '-0.0938', '0.3416', '-0.36', '-0.64', '-0.1608', '-0.15', '-0.0389', '-0.0285', '-0.0981', '-0.4697', '0.1941', '0.1311', '-0.07104', '-0.3594', '0.2179', '-0.3777', '0.3486', '-0.1879', '0.4714', '0.261', '0.1992', '-0.216', '-0.01013', '-0.146', '0.5977', '0.2394', '0.7056', '-0.096', '0.1881', '0.4316', '0.1908', '0.2108', '-0.355', '-0.2441', '0.352', '0.09265', '-0.0697', '0.4636', '-0.1278', '-0.353', '-0.03702', '-0.1696', '0.2988', '0.5796', '0.5796', '0.1329', '-0.01522', '0.2405', '-0.134', '-0.253', '0.8936', '-0.5923', '-0.014854', '0.557', '-0.04718', '0.3733', '-0.00457', '-0.49', '0.304', '0.275', '0.437', '0.785', '-0.1671', '0.1713', '-0.0964', '0.2957', '0.5977', '-0.01819', '0.2942', '-0.2339', '0.2576', '0.1449', '-0.2825', '-0.1555', '0.3557', '0.07184', '0.4182', '-0.6855', '-0.0259', '-0.2585', '0.2727', '-0.01517', '0.384', '-0.331', '0.0091', '0.2507', '-0.2517', '0.05902', '0.653', '0.12115', '0.2927', '0.10034', '0.01559', '0.1042']",C123725,,,,,,
mondo:0010265,Simpson-Golabi-Behmel syndrome type 2,"['Sgbs2', 'lethal variant of Simpson-Golabi-Behmel syndrome', 'Simpson-Golabi-Behmel syndrome caused by mutation in OFD1', 'Simpson-Golabi-Behmel syndrome, type 2', 'OFD1 Simpson-Golabi-Behmel syndrome', 'SGBS2', 'Simpson-Golabi-Behmel syndrome, type 2, X-linked recessive']",0080342,300209,79022,C1846175,"['0.03928', '0.1749', '0.434', '-0.812', '0.1152', '-0.5557', '0.03366', '0.295', '-0.4895', '-0.2751', '0.2435', '0.02728', '-0.002983', '-0.3308', '-0.466', '0.2018', '0.233', '0.2235', '-0.4744', '-0.2898', '0.04645', '-0.004787', '0.354', '-0.1093', '0.167', '-0.2864', '-0.2986', '-0.06052', '0.7134', '-0.722', '0.2847', '0.1396', '0.319', '0.1306', '0.382', '-0.11597', '-0.4019', '-0.3145', '-0.2844', '-0.2084', '-0.01345', '-0.558', '0.11115', '-0.1534', '-0.3284', '0.0454', '-0.0699', '0.3682', '-0.3003', '-0.02005', '-0.4758', '0.1375', '-0.0673', '-0.0767', '-0.4714', '-0.3704', '-0.2666', '-0.1918', '-0.1488', '-0.00654', '0.08746', '-0.05505', '-0.453', '0.2336', '0.226', '-0.2449', '0.10815', '0.1733', '-0.383', '0.54', '-0.4622', '0.007664', '0.1343', '-0.02966', '-0.2418', '0.01445', '0.1094', '-0.339', '-0.403', '-0.01383', '-0.296', '0.08295', '-0.1327', '0.3093', '-0.002329', '0.5454', '-0.2666', '0.461', '0.515', '-0.004345', '0.09924', '0.505', '0.7627', '0.2102', '0.807', '0.329', '0.3972', '-0.405', '0.3447', '-0.000854']",,,C564567,,,,
mondo:0010266,"intellectual disability, X-linked 58","['non-syndromic X-linked intellectual disability caused by mutation in TSPAN7', 'intellectual developmental disorder, X-linked 58, X-linked recessive', 'mental retardation, X-linked type 58', 'intellectual disability, X-linked 58', 'intellectual disability, X-linked type 58', 'mental retardation, X-linked 58', 'MRX58', 'TSPAN7 non-syndromic X-linked intellectual disability']",0112024,300210,,C1846174,,,,C564566,,,,
mondo:0010267,"episodic muscle weakness, X-linked","['episodic muscle weakness, X-linked', 'EMWX']",,300211,,C1846173,,,,C564565,,,,
mondo:0010268,X-linked lissencephaly with abnormal genitalia,"['XLAG syndrome', 'lissencephaly, X-linked, with ambiguous genitalia', 'hydranencephaly with abnormal genitalia', 'lissencephaly, X-linked 2', 'X-linked lissencephaly - agenesis of the corpus callosum - genital anomalies', 'X-linked lissencephaly with ambiguous genitalia', 'LISX2', 'X-linked lissencephaly-agenesis of the corpus callosum-genital anomalies syndrome', 'Xlisg', 'XLAG (X-linked lissencephaly with abnormal genitalia) syndrome', 'lissencephaly, X-linked, type 2', 'hydranencephaly and abnormal genitalia', 'lissencephaly, X-linked, 2', 'X-linked lissencephaly-corpus callosum agenesis-genital anomalies syndrome']",0112238,300215,452,,"['-0.7427', '0.1071', '0.5664', '-0.978', '0.6807', '-0.11957', '0.2413', '0.6265', '-0.4312', '-0.4014', '0.03644', '-0.825', '-0.1797', '-0.0769', '0.0714', '-0.1644', '0.627', '-0.3809', '-0.1382', '-0.346', '0.222', '-0.5386', '0.3948', '-0.635', '0.3057', '-0.17', '0.285', '-0.1263', '0.1334', '-0.11334', '0.03845', '0.1205', '0.722', '0.508', '0.3235', '-0.529', '-0.6196', '0.03104', '-0.2399', '-0.4375', '0.783', '-0.723', '-0.2247', '0.3042', '-0.1095', '-0.983', '-0.3071', '-0.0655', '-0.1343', '0.4343', '0.0546', '-0.3457', '-0.946', '0.317', '-0.152', '0.6187', '0.9204', '0.1025', '0.1805', '0.4915', '-0.5117', '0.4067', '0.4648', '0.695', '-0.4277', '0.1771', '0.6025', '0.7124', '0.176', '0.2046', '0.09076', '0.846', '0.66', '0.9014', '-0.11053', '0.5796', '0.5938', '-0.008736', '-0.05374', '-0.0873', '-0.596', '0.4734', '0.2017', '-0.247', '-0.05078', '0.2822', '0.456', '0.841', '-0.5063', '-0.5337', '-0.1482', '0.2074', '-0.229', '-0.3616', '0.6704', '0.2886', '0.4302', '-0.593', '0.6533', '0.05826']",,,C564563,,,,
mondo:0010269,Coats disease,"['Coats^ disease', 'Leber miliary aneurysm', 'exudative retinopathy', 'retinal telangiectasis', 'Coats disease', 'Coats^ syndrome', 'congenital retinal telangiectasia']",7765,300216,190,C0154832,,,,D058456,362.12,,10015901,
mondo:0010270,syndromic X-linked intellectual disability 7,"['Ahmad X-linked mental retardation syndrome', 'syndromic X-linked intellectual disability type 7', 'mental retardation, X-linked, syndromic 7', 'Ahmad X-linked intellectual disability syndrome', 'intellectual disability, X-linked syndromic 7', 'mental retardation, obesity, hypogonadism, and tapering fingers', 'mental retardation X-linked syndromic 7', 'MRXS7', 'intellectual disability, obesity, hypogonadism, and tapering fingers', 'X-linked intellectual disability, Ahmad type', 'intellectual disability X-linked syndromic 7', 'mental retardation, X-linked syndromic 7', 'intellectual disability, X-linked, syndromic 7']",0060808,300218,85274,C4304916,,,,C537449,,,,
mondo:0010271,X-linked myotubular myopathy-abnormal genitalia syndrome,"['Xq28 contiguous gene deletion syndrome', 'myotubular myopathy with abnormal genital development']",,300219,456328,C1846169,,,,C564561,,,,
mondo:0010273,"lymphoma, Hodgkin, X-linked pseudoautosomal","['Hodgkin disease, X-linked Pseudoautosomal', 'lymphoma, Hodgkin, X-linked pseudoautosomal', 'Hodgkin disease susceptibility, pseudoautosomal']",,300221,,,,,,C538326,,,,
mondo:0010274,testicular germ cell tumor 1,"['testicular germ cell tumor', 'testicular germ cell tumor 1', 'testicular germ cell tumour', 'TGCT1']",,300228,,C1846164,,,,C564559,,,,
mondo:0010275,"spondyloepimetaphyseal dysplasia, Bieganski type","['leukoencephalopathy with metaphyseal chondrodysplasia', 'spondyloepimetaphyseal dysplasia, X-linked, with hypomyelinating leukodystrophy, X-linked recessive', 'leukoencephalopathy-metaphyseal chondrodysplasia syndrome', 'spondyloepimetaphyseal dysplasia, X-linked, with mental deterioration', 'SEMD X-linked with mental deterioration', 'spondyloepimetaphyseal dysplasia X-linked with mental deterioration', 'SEMD, X-linked, with mental deterioration', 'H-SMD', 'hypomyelination-spondyloepimetaphyseal dysplasia syndrome', 'LKMCD', 'leukoencephalopathy-SEMD syndrome']",,300232,83629,C1846148,"['-0.4426', '-0.0802', '0.2876', '-0.3162', '-0.0981', '-0.5747', '-0.369', '0.354', '-0.6455', '-0.2747', '-0.00357', '-0.0454', '-0.5625', '0.2013', '0.9004', '0.1943', '0.03027', '-0.1981', '-0.2059', '-0.398', '0.3625', '-0.0094', '0.547', '0.02109', '0.02605', '0.003328', '0.1158', '0.01411', '-0.2174', '-0.03693', '0.4487', '0.01382', '0.229', '0.298', '0.3333', '-0.4402', '-0.4258', '-0.754', '-0.2347', '-0.2917', '0.2118', '-0.5356', '-0.331', '0.5664', '-0.3748', '-0.5234', '-0.0287', '0.599', '-0.1094', '-0.1572', '0.2756', '0.2395', '-0.2534', '-0.0764', '0.0474', '-0.7407', '0.2285', '-0.11', '-0.0835', '0.2659', '-0.02512', '-0.12', '-0.09216', '0.1809', '-0.5273', '-0.4065', '0.2673', '0.769', '-0.348', '0.4944', '-0.5464', '-0.441', '0.2148', '-0.655', '0.1604', '0.4167', '-0.342', '0.1674', '-0.4053', '-0.2025', '0.08685', '-0.2876', '0.1288', '1.143', '-0.4634', '0.05164', '-0.1547', '-0.1302', '0.146', '-0.03717', '0.3762', '0.1604', '0.07513', '0.4148', '0.4238', '0.5503', '0.5938', '0.2988', '0.6587', '0.3162']",,,C567065,,G11.4,,
mondo:0010276,"radioulnar synostosis, radial ray abnormalities, and severe malformations in the male","['radioulnar synostosis, radial RAY abnormalities, and severe malformations in the MALE']",,300233,,C1846147,,,,C564557,,,,
mondo:0010277,syndromic X-linked intellectual disability Shashi type,"['syndromic X-linked intellectual disability type 11', 'intellectual disability, X-linked, Shashi type', 'SMRXS', 'intellectual disability, X-linked, syndromic 11', 'intellectual disability X-linked syndromic 11', 'intellectual disability, X-linked, syndromic 11, Shashi type', 'MRXS11', 'mental retardation X-linked Shashi type', 'intellectual disability X-linked Shashi type', 'X-linked intellectual disability, Shashi type', 'Shashi X-linked intellectual disability syndrome', 'X-linked mental retardation Shashi type', 'mental retardation, X-linked, syndromic 11, Shashi type', 'Shashi X-linked mental retardation syndrome', 'X-linked intellectual disability Shashi type', 'mental retardation, X-linked, Shashi type', 'intellectual developmental disorder, syndromic 11, Shashi type, X-linked recessive', 'mental retardation, X-linked, syndromic 11', 'mental retardation X-linked syndromic 11']",0060826,300238,85286,C4305085,"['-0.2164', '0.398', '0.1009', '-0.316', '0.4414', '-0.77', '-0.09094', '0.5894', '-0.4517', '-0.4348', '-0.0397', '-0.2488', '0.2344', '-0.01942', '0.0779', '0.2347', '0.3499', '-0.05692', '-0.3835', '-0.1499', '0.12384', '-0.04123', '0.3032', '-0.496', '0.2751', '-0.2023', '-0.323', '-0.11066', '0.4607', '-0.4587', '0.671', '-0.1448', '0.196', '0.1005', '0.00875', '-0.331', '-0.2', '-0.4402', '-0.205', '-0.4128', '0.4204', '-0.3381', '-0.4668', '0.1144', '-0.02426', '-0.1259', '0.296', '0.2484', '-0.3616', '-0.5513', '-0.3047', '-0.1298', '-0.1493', '0.1653', '0.02658', '-0.3906', '0.5337', '0.065', '-0.03793', '0.2457', '-0.3145', '0.07434', '-0.1209', '0.4038', '-0.0776', '0.04428', '-0.1294', '0.2905', '-0.492', '0.1619', '-0.3662', '0.2028', '0.263', '-0.08453', '-0.1017', '0.381', '-0.1991', '0.0712', '-0.1346', '0.2952', '0.1805', '0.0913', '-0.03345', '0.3113', '0.1868', '0.52', '0.01331', '0.5215', '0.386', '0.4526', '-0.2612', '0.7104', '0.2712', '-0.1348', '1.039', '-0.06335', '-0.2301', '-0.8013', '0.3284', '-0.2094']",,,C537135,,,,
mondo:0010278,Christianson syndrome,"['mental retardation, X-linked syndromic, Christianson type', 'MRXSCH', 'X-linked intellectual disability-craniofacial dysmorphism-epilepsy-ophthalmoplegia-cerebellar atrophy syndrome', 'X-linked Angelman-like syndrome', 'X-linked intellectual disability, South African type', 'intellectual developmental disorder, X-linked syndromic, Christianson type', 'mental retardation, microcephaly, epilepsy, and ataxia syndrome', 'MRXS Christianson', 'X-linked intellectual disability - craniofacial dysmorphism - epilepsy - ophthalmoplegia - cerebellar atrophy', 'Angelman-like syndrome X-linked', 'intellectual disability X-linked syndromic Christianson type', 'intellectual disability, X-linked syndromic, Christianson type', 'intellectual disability, X-linked, syndromic, Christianson type', 'Angelman-like syndrome, X-linked', 'mental retardation, X-linked, syndromic, Christianson type', 'intellectual disability microcephaly epilepsy and ataxia syndrome', 'intellectual disability, microcephaly, epilepsy, and ataxia syndrome']",0060825,300243,85278,C2678194,"['-0.03894', '0.6284', '0.0435', '-0.45', '-0.07135', '-0.614', '0.1409', '0.9385', '-0.8975', '-0.4663', '-0.1702', '-0.11066', '0.0618', '0.07495', '0.5635', '0.02193', '0.2241', '-0.0885', '-0.05563', '-0.6064', '-0.2239', '-0.0335', '0.2898', '-0.406', '0.1101', '0.07367', '-0.1886', '-0.02979', '0.2693', '-0.1678', '0.12244', '-0.1322', '0.6816', '0.1887', '-0.12445', '0.08704', '0.04135', '-0.2834', '-0.5894', '0.1508', '0.00706', '-0.1315', '-0.02336', '-0.08105', '0.3564', '-0.4148', '-0.3672', '-0.11035', '-0.2346', '0.435', '-0.2886', '0.4224', '-0.4387', '-0.7026', '0.245', '0.4258', '-0.03275', '-0.2367', '0.1693', '0.05994', '0.2465', '0.214', '0.3193', '0.245', '-0.0001332', '0.1976', '0.4956', '-0.0636', '-0.3677', '0.2285', '-0.2003', '0.3528', '-0.0642', '0.1709', '0.01921', '-0.2047', '0.6147', '-0.0995', '-0.3499', '0.1128', '0.0732', '0.10876', '-0.368', '0.5796', '0.384', '0.2761', '0.1366', '0.3706', '0.4946', '0.6147', '0.08936', '0.298', '0.04346', '-0.2793', '0.3652', '-0.1576', '0.2795', '0.0708', '0.2421', '0.133']",,,C567484,759.89,,,
mondo:0010279,terminal osseous dysplasia-pigmentary defects syndrome,"['TOD', 'terminal osseous dysplasia', 'osseous dysplasia, digital, with Facial pigmentary defects and multiple frenula', 'terminal osseous dysplasia and pigmentary defects', 'Odpf syndrome', 'terminal osseous dysplasia, X-linked dominant', 'Odpd']",0112149,300244,88630,C1846129,"['-0.2844', '0.015175', '-0.1119', '0.2181', '0.5', '-0.839', '-0.11975', '0.503', '-0.315', '-0.4524', '-0.5703', '0.3591', '-0.2015', '-0.122', '0.1305', '0.3877', '0.2844', '-0.1871', '-0.1164', '-0.222', '-0.1938', '0.015495', '0.3823', '-0.3738', '0.05704', '-0.1924', '-0.336', '0.267', '0.05978', '-0.01371', '0.4634', '-0.4526', '-0.3264', '-0.1292', '0.328', '-0.07556', '-0.1477', '-0.408', '-0.2686', '0.0668', '0.05966', '-0.4749', '0.09155', '-0.573', '0.0865', '-0.268', '-0.326', '0.6274', '-0.1564', '-0.2202', '-0.262', '0.02419', '0.1076', '0.1395', '-0.3323', '-0.848', '0.0992', '0.06964', '-0.08887', '0.1021', '0.1886', '-0.4553', '-0.0616', '0.1947', '-0.3757', '0.11725', '0.3936', '0.599', '-0.5186', '0.1663', '-0.1508', '-0.05222', '0.2847', '0.1643', '0.0556', '0.03035', '0.05283', '-0.02605', '0.2019', '-0.4836', '0.0427', '-0.0724', '0.3784', '0.3926', '0.03955', '0.1167', '0.1935', '0.786', '0.05563', '0.08813', '0.05756', '0.4', '0.1362', '0.01108', '0.395', '-0.0854', '0.4502', '-0.9033', '0.5024', '0.05283']",,,C564554,,,,
mondo:0010280,"ptosis, hereditary congenital 2","['Ptos2', 'ptosis, hereditary congenital type 2', 'ptosis, X-linked', 'ptosis, hereditary congenital 2', 'ptosis, hereditary congenital 2, X-linked dominant']",,300245,,C1846128,,,,C564553,,,,
mondo:0010281,Danon disease,"['glycogenosis due to LAMP-2 deficiency', 'GSD due to LAMP-2 deficiency', 'Danon disease, X-linked dominant', 'lysosomal glycogen storage disease without acid maltase deficiency', 'GSD2B (formerly)', 'lysosomal glycogen storage disease with normal acid maltase activity', 'X-linked vacuolar cardiomyopathy and myopathy', 'glycogen storage disease IIb', 'LAMP2 lysosomal glycogen storage disease', 'glycogen storage disease type 2b (formerly)', 'glycogen storage disease due to LAMP-2 deficiency', 'GSD IIb', 'ANTOPOL disease', 'vacuolar cardiomyopathy and myopathy X-linked', 'glycogen storage cardiomyopathy', 'GSD IIb, formerly', 'glycogen storage disease limited to the heart', 'Danon disease', 'pseudoglycogenosis II', 'Antopol disease', 'lysosomal glycogen storage disease without acid maltase deficiency, formerly', 'glycogen storage disease type IIb', 'lysosomal glycogen storage disease without acid maltase deficiency (formerly)', 'vacuolar cardiomyopathy and myopathy, X-linked', 'pseudoglycogenosis 2']",0050437,300257,34587,C0878677,"['0.1052', '0.1616', '-0.6934', '-0.00907', '0.4036', '-0.545', '0.002316', '0.6997', '-0.825', '-0.5127', '-0.1869', '-0.4', '0.01903', '0.05316', '-0.478', '0.1443', '-0.1873', '0.06036', '-0.5557', '-0.2698', '0.496', '-0.2632', '0.8486', '0.03784', '-0.2576', '-0.04987', '0.1831', '-0.234', '0.1641', '0.4685', '0.712', '-0.1484', '0.2698', '0.3513', '0.11255', '-0.583', '-0.1362', '-0.09796', '-0.11127', '0.2007', '-0.1412', '-0.4233', '-0.00919', '0.5225', '-0.1392', '0.1018', '-0.3618', '-0.037', '-0.7266', '0.2944', '-0.01974', '0.1517', '0.2426', '-0.011284', '-0.011894', '-0.541', '0.419', '0.00374', '-0.355', '0.1505', '0.3018', '-0.4714', '0.4866', '-0.2357', '-0.4277', '0.0505', '0.03052', '0.3958', '-0.6235', '-0.04648', '-0.1976', '-0.4744', '-0.06183', '0.5557', '0.7974', '-0.02248', '0.2119', '0.2583', '-0.3525', '0.01257', '0.02983', '-0.1285', '-0.04718', '-0.0388', '0.1146', '0.4512', '0.1066', '0.1454', '0.4316', '0.02576', '0.7925', '-0.02899', '-0.03622', '-0.095', '0.8525', '0.4895', '0.4854', '-0.387', '0.1685', '0.202']",C84735,1001333,D052120,759.89,,,
mondo:0010282,"mycobacterium tuberculosis, susceptibility to, X-linked","['MTBSX', 'mycobacterium tuberculosis, susceptibility, X-linked', 'mycobacterium tuberculosis, susceptibility to, X-linked']",,300259,,,,,,,,,,
mondo:0010283,syndromic X-linked intellectual disability Lubs type,"['MRXSL', 'XLMR syndrome, Lubs type', 'Lubs X-linked mental retardation syndrome (formerly)', 'mental retardation, X-linked, Lubs type (formerly)', 'distal duplication Xq', 'MECP2 Duplication syndrome', 'mental retardation, X-linked, with recurrent respiratory infections', 'intellectual disability, X-linked, with recurrent respiratory infections', 'intellectual developmental disorder, X-linked syndromic, Lubs type, X-linked recessive', 'intellectual disability, X-linked, Lubs type (formerly)', 'trisomy Xq28', 'MECP2 duplication syndrome', 'intellectual disability, X-linked, syndromic, Lubs type', 'mental retardation, X-linked, syndromic, Lubs type', 'X-linked intellectual disability-hypotonia-recurrent infections syndrome', 'Lubs X-linked mental retardation syndrome', 'Lubs X-linked intellectual disability syndrome (formerly)', 'telomeric duplication Xq', 'Xq28 (MECP2) duplication', 'Lubs X-linked intellectual disability syndrome']",0060799,300260,1762,C1846058,,C126747,,C537723,758.89,,,
mondo:0010284,Armfield syndrome,"['Armfield syndrome', 'MRXSA', 'intellectual disability, X-linked, syndromic, Armfield type', 'intellectual disability syndrome, X-linked, Armfield type', 'intellectual developmental disorder, X-linked, syndromic, Armfield type, X-linked recessive', 'Armfield X-linked intellectual disability syndrome', 'syndromic X-linked intellectual disability Armfield type', 'syndromic X-linked mental retardation Armfield type', 'X-linked intellectual disability, Armfield type', 'Armfield X-linked mental retardation syndrome', 'mental retardation, X-linked, syndromic, Armfield type', 'mental retardation syndrome, X-linked, armfield type, X-linked recessive', 'mental retardation syndrome, X-linked, Armfield type']",0050764,300261,85276,C1846057,,,,C564551,,,,
mondo:0010285,syndromic X-linked intellectual disability Abidi type,"['mental retardation, X-linked, syndromic, Abidi type', 'MRXSAB', 'intellectual disability X-linked Abidi type', 'syndromic X-linked intellectual disability Abidi type', 'ABIDI X-linked intellectual disability syndrome', 'intellectual disability, X-linked, syndromic, Abidi type', 'intellectual disability, X-linked syndromic, Abidi type', 'syndromic X-linked mental retardation Abidi type', 'ABIDI X-linked mental retardation syndrome', 'short stature, small head circumference, sloping forehead, hearing loss, cupped ears and small testes', 'X-linked intellectual disability, Abidi type', 'mental retardation, X-linked syndromic, Abidi type']",0060818,300262,85273,C1846056,,,,C535556,,,,
mondo:0010286,syndromic X-linked intellectual disability Siderius type,"['Siderius-Hamel syndrome', 'X-linked mental retardation Hamel type', 'MRXSSD', 'intellectual deficit X-linked Siderius type', 'intellectual disability syndrome, X-linked, Siderius type', 'X-linked intellectual disability Hamel type', 'intellectual developmental disorder, X-linked, syndromic, Siderius type, X-linked recessive', 'Siderius Hamel syndrome', 'mental retardation syndrome, X-linked, Siderius type', 'X-linked intellectual disability, Siderius type', 'intellectual disability X-linked Siderius type', 'mental retardation, X-linked, syndromic, Siderius type', 'Siderius X-linked mental retardation syndrome', 'mental retardation X-linked Siderius type', 'Siderius X-linked intellectual disability syndrome', 'intellectual disability, X-linked, syndromic, Siderius type']",0060812,300263,85287,C1846055,"['-0.039', '0.1715', '0.0895', '-0.3345', '0.4', '-0.4597', '-0.1858', '0.308', '-0.269', '-0.494', '-0.04544', '-0.0765', '0.05743', '-0.0598', '0.09955', '0.0945', '0.10846', '-0.2974', '-0.3008', '-0.303', '0.02222', '0.1499', '0.2869', '-0.3591', '0.3115', '-0.1077', '-0.2805', '-0.05936', '0.4507', '-0.2754', '0.3474', '-0.2444', '0.2242', '0.1004', '0.1857', '-0.4417', '-0.075', '-0.395', '-0.1658', '-0.166', '0.1193', '-0.2045', '-0.2186', '-0.1162', '-0.0616', '-0.2236', '0.0536', '0.1407', '-0.11743', '-0.3074', '-0.2079', '-0.1884', '-0.1553', '0.01773', '0.01717', '-0.1659', '0.3289', '0.003786', '-0.10443', '0.3853', '-0.0009627', '0.01511', '0.10364', '0.3745', '-0.1589', '0.0729', '-0.01451', '0.4094', '-0.3823', '0.1134', '-0.381', '0.1245', '0.10504', '-0.0209', '0.11786', '0.267', '0.05093', '0.03366', '-0.2119', '0.1207', '0.153', '0.1315', '0.06186', '0.3616', '0.03857', '0.1975', '0.07227', '0.5825', '0.08923', '0.2786', '-0.1543', '0.5186', '0.1729', '-0.3062', '0.7163', '-0.01689', '0.1321', '-0.6846', '0.2852', '0.0964']",,,C537333,,,,
mondo:0010287,hereditary spastic paraplegia 16,"['SPG16', 'X-linked spastic paraplegia type 16', 'spastic paraplegia 16, X-linked, complicated, X-linked recessive', 'X-linked spastic paraplegia 16', 'hereditary spastic paraplegia type 16', 'spastic paraplegia 16, X-linked', 'spastic paraplegia 16']",0110769,300266,100997,C1846046,,,,C536643,,,,
mondo:0010288,adrenomyodystrophy,['adrenomyodystrophy'],,300270,977,C1846044,,,,C538051,,,,
mondo:0010289,"intellectual disability, X-linked 72","['mental retardation, X-linked 72', 'mental retardation, X-linked type 72', 'intellectual disability, X-linked 72', 'MRX72', 'intellectual disability, X-linked type 72', 'intellectual developmental disorder, X-linked 72, X-linked recessive']",0112059,300271,,C1846038,,,,C564547,,,,
mondo:0010290,"goiter, multinodular 2","['MNG2', 'goiter, multinodular, 2, X-linked dominant', 'goiter, multinodular 2']",,300273,,C1846033,,,,C564546,,,,
mondo:0010292,Uruguay Faciocardiomusculoskeletal syndrome,"['faciocardiomusculoskeletal syndrome, Uruguay type', 'FCMSU', 'uruguay faciocardiomusculoskeletal syndrome, X-linked recessive', 'Fcms', 'Uruguay Faciocardiomusculoskeletal syndrome', 'URUGUAY FACIOCARDIOMUSCULOSKELETAL syndrome']",0112148,300280,,C1846010,"['-0.01263', '0.01337', '0.00739', '0.0009103', '0.00594', '-0.01733', '0.00808', '0.01301', '-0.01791', '0.00391', '0.00964', '0.002958', '-0.003588', '-0.003994', '-0.005127', '0.0001035', '0.005924', '-0.003096', '0.003534', '-0.01551', '-0.0042', '-0.004913', '0.006504', '-0.003246', '0.006462', '0.00699', '-0.001537', '-0.001594', '0.009705', '-0.01334', '0.00718', '-0.00938', '0.01066', '0.01043', '0.00618', '-0.0001893', '-0.0105', '-0.002394', '-0.006554', '-0.016', '0.0051', '-0.01002', '0.003933', '-0.01284', '0.006294', '-0.001587', '-0.00823', '0.002893', '0.00892', '-0.001282', '-0.013306', '-0.007458', '0.007195', '-0.010376', '-0.00834', '-0.00281', '0.0144', '-0.0052', '4.274e-05', '0.004204', '0.002522', '0.002794', '0.002628', '0.003628', '0.004547', '0.00075', '0.007797', '0.00517', '-0.01689', '0.01011', '-0.01319', '0.00484', '0.00487', '0.0009604', '0.01168', '0.002821', '0.00802', '0.00514', '-0.002598', '0.003069', '-0.003998', '-0.003502', '-0.01324', '0.003803', '-0.00406', '-0.00619', '-0.005432', '0.01756', '0.007523', '0.01331', '0.005257', '0.01636', '0.003227', '0.00654', '0.02303', '-0.000987', '0.000686', '-0.01101', '-0.00909', '0.01518']",,,C564544,,,,
mondo:0010293,ectodermal dysplasia and immune deficiency,"['anhidrotic ectodermal dysplasia with immune deficiency', 'hypohidrotic ectodermal dysplasia with immune deficiency', 'hypohidrotic ectodermal dysplasia with immunodeficiency', 'ectodermal dysplasia, hypohidrotic, with immune deficiency', 'HED-ID', 'ectodermal dysplasia, anhidrotic, with immune deficiency', 'Xhm-Ed', 'EDA-ID', 'anhidrotic ectodermal dysplasia with immunodeficiency', 'hyper-IgM immunodeficiency, X-linked, with hypohidrotic ectodermal dysplasia']",0081077,,98813,C1846006,"['0.1256', '0.4644', '0.3987', '-0.7246', '0.4473', '-0.2778', '-0.0801', '0.1862', '-0.02626', '-0.759', '0.245', '-0.1785', '-0.5444', '0.1754', '-0.05356', '0.3264', '0.355', '-0.1453', '-0.6113', '-0.3853', '-0.09106', '-0.137', '1.02', '-0.05865', '0.05658', '0.1733', '-0.6064', '-0.1288', '0.0858', '-0.4404', '0.3853', '0.313', '0.03622', '-0.1948', '0.1641', '0.03915', '-0.6245', '0.2', '-0.2341', '-0.362', '0.3755', '0.010704', '-0.2756', '-0.6733', '0.0715', '-0.5273', '0.2908', '-0.2411', '0.346', '-0.0414', '0.5425', '-0.1608', '0.2905', '0.01326', '-0.5317', '-0.0723', '0.5166', '-0.619', '0.0853', '-0.2488', '-0.1799', '0.3677', '-0.1511', '-0.1543', '0.501', '0.129', '0.4329', '0.384', '-0.485', '0.4788', '-0.702', '-0.1222', '0.03055', '-0.1293', '-0.10974', '0.3333', '-0.02275', '0.02673', '0.1187', '-0.2576', '0.1159', '-0.0081', '0.792', '-0.05722', '-0.2842', '0.03162', '0.04224', '-0.1812', '-0.05392', '0.5566', '0.184', '0.395', '0.007668', '0.4854', '0.5605', '0.516', '-0.1242', '0.06964', '-0.06067', '0.6367']",C118844,,C536181,,,,
mondo:0010294,X-linked severe congenital neutropenia,"['severe congenital neutropenia, X-linked', 'Xln', 'neutropenia, severe congenital, X-linked', 'SCNX', 'severe congenital neutropenia X-linked', 'neutropenia, severe congenital, X-linked, X-linked recessive']",0112128,300299,86788,C1845987,"['-0.1228', '0.2769', '-0.3313', '-0.4214', '0.1098', '-0.4448', '-0.0096', '0.08765', '0.0963', '-0.844', '0.10126', '0.1565', '0.08966', '-0.05573', '-0.2695', '0.09186', '-0.168', '0.3381', '-0.59', '-0.3794', '-0.00505', '0.0759', '0.6196', '-0.412', '0.2878', '-0.257', '-0.2417', '-0.11017', '0.3127', '-0.6245', '0.09674', '0.06903', '0.2014', '-0.2496', '-0.11725', '-0.3374', '-0.4907', '-0.6826', '-0.414', '-0.6025', '-0.2737', '-0.05862', '0.1616', '-0.269', '-0.2458', '-0.3062', '-0.2905', '-0.2317', '-0.1907', '-0.1779', '-0.1259', '-0.2554', '0.3638', '-0.1008', '0.5293', '-0.4443', '0.971', '0.0683', '-0.3914', '0.3296', '-0.0682', '0.2274', '0.4036', '0.4128', '0.713', '-0.3792', '0.11633', '-0.004562', '-1.008', '0.2062', '-0.622', '0.02156', '-0.3127', '0.08014', '0.08795', '-0.03403', '0.3396', '0.7324', '0.3496', '0.1433', '-0.2104', '0.3193', '-0.0932', '0.3567', '0.1517', '0.0459', '0.379', '0.8926', '0.1843', '0.00867', '-0.129', '0.917', '0.2429', '0.1033', '1.164', '0.617', '0.139', '-1.27', '-0.159', '-0.3188']",,,C564539,,,,
mondo:0010295,anhidrotic ectodermal dysplasia-immunodeficiency-osteopetrosis-lymphedema syndrome,"['OLEDAID', 'ol-EDA-ID', 'ectodermal dysplasia, anhidrotic, with immunodeficiency, osteopetrosis, and lymphedema']",,300301,69088,,,,,C564538,,,,
mondo:0010296,immunodeficiency 61,"['AGMX2', 'XLA2', 'immunodeficiency 61, X-linked recessive', 'agammaglobulinemia X-linked type 2', 'agammaglobulinemia, X-linked, type 2']",0111999,300310,,C1845903,,,,C538057,,,,
mondo:0010297,FG syndrome 2,"['FG syndrome 2', 'FLNA FG syndrome', 'FG syndrome caused by mutation in FLNA', 'FGS2', 'FG syndrome type 2']",,300321,,C1845902,,,,,,,,
mondo:0010298,Lesch-Nyhan syndrome,"['complete hypoxanthine-guanine phosphoribosyltransferase deficiency', 'deficiency of IMP pyrophosphorylase', 'HPRT deficiency, complete', 'HPRT complete deficiency', 'Lesch-Nyhan syndrome, neurologic variant', 'LNS', 'hypoxanthine-guanine-phosphoribosyltransferase deficiency (& [Lesch - Nyhan syndrome])', 'HPRT deficiency grade IV', 'Lesch-Nyhan syndrome, X-linked recessive', 'Lesch Nyhan disease', 'Lesch Nyhan syndrome', 'Lesch-Nyhan syndrome', 'HPRT deficiency', 'HPRT deficiency, neurologic variant', 'hypoxanthine guanine phosphoribosyltransferase 1 deficiency', 'Lesch - Nyhan syndrome', 'X-linked hyperuricemia (disorder) [ambiguous]', 'X-linked hyperuricemia', 'hypoxanthine guanine phosphoribosyltransferase complete deficiency', 'Hprt1 deficiency', 'hypoxanthine guanine phosphoribosyltransferase deficiency, grade IV', 'HG-PRT deficiency', 'hypoxanthine guanine phospho-ribosyltransferase 1 deficiency']",1919,300322,510,CN205196,"['0.441', '0.4668', '0.1392', '-0.3484', '-0.1487', '-0.3772', '-0.4783', '0.6826', '-0.944', '-0.08875', '0.289', '0.09503', '0.05106', '0.1709', '-0.01292', '0.01537', '-0.1395', '-0.3547', '0.278', '-0.7393', '-0.252', '-0.1637', '0.692', '-0.2104', '-0.5376', '-0.423', '0.0615', '0.2336', '0.4219', '0.3098', '-0.3232', '-0.03017', '0.1274', '0.5474', '-0.8433', '-0.3281', '-0.3643', '-0.541', '-0.4001', '0.1293', '0.1984', '-0.5806', '-0.01181', '0.4548', '0.368', '-0.2075', '-0.006504', '0.1958', '0.4062', '1.127', '-0.861', '0.2091', '0.1262', '-0.55', '0.09314', '0.0598', '0.4934', '-0.4463', '-0.3538', '0.2998', '0.03653', '0.07666', '-0.0699', '0.1565', '0.324', '-0.05038', '0.689', '-0.2026', '-0.2576', '0.2433', '0.2986', '0.074', '-0.538', '-0.6113', '0.234', '0.423', '-0.010155', '-0.4312', '-0.5093', '-0.1553', '-0.3264', '-0.3645', '0.3914', '0.1962', '0.2764', '0.518', '-0.9307', '-0.3591', '0.05725', '0.6284', '0.3154', '0.1581', '-0.233', '-0.1929', '0.0742', '0.254', '0.07733', '-0.1823', '0.1981', '0.815']",C61255,,D007926,277.2,E79.1,10057589,
mondo:0010299,hypoxanthine guanine phosphoribosyltransferase partial deficiency,"['HPRT-related hyperuricemia', 'hypoxanthine guanine phosphoribosyltransferase deficiency, grade I', 'HPRT deficiency, partial', 'HPRT-related gout', 'KELLEY-Seegmiller syndrome', 'HPRT deficiency, grade I', 'Kelley-Seegmiller syndrome', 'Hprt1 deficiency, partial', 'gout, HPRT-related', 'hypoxanthine guanine phosphoribosyltransferase 1 partial deficiency', 'HPRT1 partial deficiency', 'HPRT partial deficiency', 'hyperuricemia, HRPT-related, X-linked recessive', 'hypoxanthine guanine phosphoribosyltransferase 1 deficiency, partial']",0112127,300323,79233,C0268117,"['0.0876', '0.4482', '0.01057', '-0.4585', '-0.2854', '-0.2651', '-0.503', '0.549', '-0.3074', '0.3738', '0.3147', '0.0798', '0.0985', '0.2603', '0.1752', '-0.2751', '0.3813', '-0.193', '0.1736', '-0.8354', '-0.329', '0.0194', '0.869', '-0.114', '-0.3423', '0.05902', '0.01135', '0.00779', '0.7246', '-0.18', '-0.3862', '-0.6836', '0.5625', '0.2001', '-0.2761', '-0.593', '-0.265', '-0.04245', '-0.3142', '0.286', '0.3716', '-0.562', '0.5537', '-0.165', '-0.0659', '-0.2079', '-0.1852', '0.01395', '0.06866', '0.987', '-0.01978', '0.10077', '0.383', '-0.5864', '0.1687', '0.3274', '0.7266', '-0.636', '-0.2137', '0.5093', '0.2435', '0.3105', '0.2218', '-0.3', '0.6445', '-0.1047', '0.573', '0.3103', '0.010376', '0.0317', '-0.1048', '-0.5044', '0.0314', '-0.3032', '0.4104', '0.426', '0.0396', '-0.0531', '-0.5723', '-0.0717', '-0.1028', '0.1603', '0.10425', '0.1454', '0.302', '0.2245', '-0.554', '-0.5713', '0.06946', '0.4502', '0.2135', '0.5547', '-0.1322', '-0.1787', '0.325', '0.3142', '0.2372', '-0.669', '-0.499', '0.1236']",,,C562583,277.2,,,
mondo:0010300,"intellectual disability, X-linked 53","['MRX53', 'mental retardation, X-linked 53', 'intellectual disability, X-linked 53', 'mental retardation, X-linked 53, X-linked recessive']",0112047,300324,,C1845889,,,,C564533,,,,
mondo:0010302,Ito hypomelanosis,"['Ito hypomelanosis', 'hi syndrome', 'HMI', 'Incontinentia pigmenti achromians', 'Ito', 'pigmentary mosaicism, Ito type', 'Incontinentia pigmenti type 1', 'hypomelanosis of Ito', 'Incontinentia pigmenti type 1 (formerly)', 'IPA', 'Incontinentia pigmenti, type I, formerly', 'Incontinentia pigmenti, type I']",3156,300337,435,C0022283,,,,,,,,
mondo:0010304,"Graves disease, susceptibility to, X-linked 1","['Grdx1', 'Graves disease, susceptibility to, X-linked type 1', 'Graves disease, susceptibility to, X-linked 2', 'Graves disease, susceptibility to, X-linked 1', 'Graves disease, susceptibility to, X-linked']",,300351,,,,,,,,,,
mondo:0010305,creatine transporter deficiency,"['cerebral creatine deficiency syndrome 1, X-linked recessive', 'mental retardation, X-linked, with creatine transport deficiency', 'CCDS1', 'X-linked creatine transporter deficiency', 'creatine transporter deficiency', 'intellectual disability, X-linked, with creatine transport deficiency', 'creatine deficiency syndrome, X-linked', 'mental retardation, X-linked, with seizures, short stature, and midface hypoplasia', 'creatine deficiency, X-linked', 'cerebral creatine deficiency syndrome 1', 'cerebral creatine deficiency syndrome type 1', 'mental retardation, X-linked, with creatine Transport deficiency', 'mental retardation, X-linked with seizures, short stature and midface hypoplasia', 'X-linked creatine deficiency syndrome', 'intellectual disability, X-linked, with creatine Transport deficiency', 'intellectual disability, X-linked, with seizures, short stature, and midface hypoplasia', 'SLC6A8 deficiency', 'X-linked creatine deficiency', 'creatine transporter defect', 'intellectual disability, X-linked with seizures, short stature and midface hypoplasia']",0050800,300352,52503,,"['-0.0762', '-0.3', '0.07733', '-0.485', '0.05878', '-0.241', '0.1023', '1.102', '-0.4656', '-0.752', '-0.339', '-0.2673', '-0.02989', '0.01256', '0.2023', '0.2323', '-0.1605', '-0.2979', '-0.6587', '-0.5747', '0.6016', '-0.3953', '0.2026', '0.0724', '0.1017', '-0.2299', '-0.1652', '-0.56', '-0.2964', '-0.2568', '0.722', '-0.7427', '0.593', '-0.1368', '-0.0978', '0.2031', '0.03348', '-0.2861', '-0.06305', '-0.2483', '0.2123', '-0.4172', '-0.1647', '0.1183', '0.0461', '-0.2332', '0.3718', '-0.006374', '0.0765', '0.1812', '-0.0806', '0.09735', '-0.2708', '0.1306', '0.2389', '0.0445', '0.01591', '-0.256', '0.1501', '0.742', '0.039', '0.2346', '0.6377', '-0.2805', '-0.4543', '0.2096', '0.0594', '0.497', '-0.2688', '0.2433', '0.2089', '-0.1624', '-0.4548', '0.4673', '0.2429', '0.689', '0.2482', '-0.4688', '-0.1287', '0.0673', '0.4067', '-0.02084', '0.513', '0.211', '0.4946', '0.628', '-0.4438', '0.08826', '0.569', '0.334', '-0.1437', '0.866', '0.06445', '-0.3337', '0.1707', '0.3533', '-0.02473', '-0.4385', '0.414', '-0.2489']",C125665,,C535598,758.81,,,
mondo:0010306,"X-linked intellectual disability, Cabezas type","['X-linked intellectual disability with short stature, hypogonadism, and abnormal gait', 'Cabezas type of X-linked syndromic intellectual disability', 'Cabezas syndrome', 'X-linked mental retardation with short stature', 'Cul4B-related X-linked intellectual disability', 'mental retardation, X-linked, with short stature, hypogonadism, and abnormal Gait', 'syndromic X-linked intellectual disability Cabezas type', 'X-linked mental retardation with short stature, hypogonadism, and abnormal gait', 'mental retardation, X-linked, syndromic, Cabezas type', 'intellectual disability, X-linked, with short stature', 'Cabezas syndrome; syndromic X-linked mental retardation 15', 'intellectual disability, X-linked, syndromic, Cabezas type', 'MRXSC', 'MRXS15', 'mental retardation, X-linked, with short stature', 'Cabezas syndrome; syndromic X-linked intellectual disability 15', 'mental retardation, X-linked, syndromic 15 (Cabezas type), X-linked recessive', 'intellectual disability, X-linked, syndromic 15', 'mental retardation, X-linked, syndromic 15 (Cabezas type)', 'intellectual disability, X-linked, with short stature, hypogonadism, and abnormal Gait', 'MRSS', 'X-linked intellectual disability with short stature', 'intellectual disability, X-linked, syndromic 15 (Cabezas type)', 'mental retardation, X-linked, syndromic 15']",0060822,300354,85293,C1845861,"['-0.1346', '0.54', '0.711', '-0.5054', '0.1613', '-0.4746', '0.2196', '0.61', '-0.4617', '-0.959', '0.0598', '-0.00563', '0.06604', '-0.2173', '0.4956', '0.5674', '0.1704', '-0.155', '-0.6304', '-0.4453', '0.2198', '-0.01674', '0.45', '0.007256', '0.1274', '-0.5645', '-0.2695', '-0.43', '0.3005', '-0.4177', '0.8545', '-0.622', '0.408', '0.0485', '-0.2213', '0.253', '-0.3665', '-0.6396', '-0.3093', '-0.09045', '0.274', '-0.00148', '-0.344', '0.2025', '0.4604', '-0.681', '-0.2673', '0.1582', '-0.2507', '-0.04684', '-0.337', '0.3665', '-0.59', '-0.0379', '0.09814', '0.02501', '0.6104', '-0.1792', '-0.1342', '0.3113', '-0.4055', '0.3525', '0.1449', '0.3918', '-0.3086', '0.4102', '-0.1871', '0.1938', '-0.002329', '-0.00912', '-0.3577', '0.228', '-0.516', '0.5283', '0.03708', '-0.0547', '0.2465', '0.03717', '-0.0468', '0.11395', '0.1026', '-0.171', '0.4824', '0.5557', '0.1475', '0.7905', '0.1841', '-0.0094', '0.498', '0.407', '-0.67', '0.613', '-0.195', '-0.1743', '0.8794', '-0.1838', '0.2036', '-0.545', '0.4775', '0.1696']",,,,,,,
mondo:0010307,"intellectual disability, X-linked 73","['mental retardation, X-linked 73', 'mental retardation, X-linked 73, X-linked recessive', 'intellectual disability, X-linked 73', 'MRX73']",0112017,300355,,C1845860,,,,C564528,,,,
mondo:0010308,"thrombocytopenia, X-linked, with or without dyserythropoietic anemia","['thrombocytopenia, X-linked, with or without dyserythropoietic anemia', 'thrombocytopenia, X-linked, with or without dyserythropoietic anemia, X-linked recessive', 'XLTDA', 'X-linked thrombocytopenia, with or without dyserythropoietic Anaemia', 'X-linked thrombocytopenia, with or without dyserythropoietic Anemia']",,300367,,C3550789,"['-0.06805', '0.1365', '-0.01287', '-0.0948', '0.0936', '-0.10156', '-0.0733', '0.1377', '-0.03076', '-0.117', '-0.04117', '-0.04233', '0.05008', '0.01451', '-0.05344', '-0.09607', '-0.04135', '-0.054', '-0.06616', '-0.2347', '-0.005424', '-0.03708', '0.1477', '-0.02275', '0.04007', '-0.0586', '0.0586', '-0.0458', '0.0821', '-0.04608', '0.0346', '-0.01576', '0.1658', '0.1313', '-0.003643', '-0.08124', '-0.1346', '-0.1666', '-0.0784', '-0.1305', '-0.06506', '-0.11554', '0.11835', '-0.0695', '-0.05545', '-0.1495', '-0.05554', '0.0403', '-0.01845', '-0.02184', '-0.0338', '-0.01505', '0.0961', '0.07733', '-0.01182', '-0.03973', '0.0797', '-0.04535', '-0.203', '0.03069', '0.08246', '0.01833', '0.05908', '-0.02774', '-0.01408', '-0.0585', '0.1318', '0.1357', '-0.09033', '0.1866', '-0.0848', '-0.05673', '-0.02899', '-0.1309', '0.07715', '0.00859', '0.05795', '-0.05432', '-0.04633', '-0.05026', '-0.01639', '-0.04163', '0.01396', '0.0243', '0.00924', '0.04926', '0.05222', '0.1803', '0.0886', '0.003841', '0.07874', '0.08966', '0.0354', '-0.02649', '0.2474', '0.1719', '0.0481', '-0.1628', '0.0374', '0.04053']",C136653,,,,,,
mondo:0010309,"intellectual disability, X-linked 42","['mental retardation, X-linked 42', 'MRX42', 'intellectual disability, X-linked 42']",0112057,300372,,C1845810,,,,C564524,,,,
mondo:0010310,osteopathia striata with cranial sclerosis,"['Osteopathia striata with cranial sclerosis, X-linked dominant', 'hyperostosis generalisata with striations', 'osteopathia striata - cranial sclerosis', 'osteopathia striata-cranial sclerosis syndrome', 'osteopathia striata cranial sclerosis', 'Robinow-Unger syndrome', 'osteopathia striata with cranial sclerosis', 'OSCS']",0060886,300373,2780,C0432268,"['-0.318', '0.1842', '0.2316', '-0.1691', '-0.03952', '-0.08325', '0.527', '0.7603', '-0.5635', '0.01993', '-0.1862', '-0.431', '0.0425', '-0.01081', '0.1514', '-0.11816', '0.01174', '-0.1687', '-0.323', '-0.4658', '0.5947', '0.1464', '0.502', '-0.0708', '-0.05426', '0.0914', '-0.2559', '0.4072', '0.1448', '0.10706', '0.04208', '-0.3308', '0.2593', '0.2109', '0.4487', '-0.8213', '-0.1142', '-0.7876', '-0.3435', '-0.3625', '0.1243', '-0.2603', '0.241', '-0.7495', '0.1798', '0.0875', '0.0309', '0.2378', '-0.4014', '-0.396', '-0.0682', '0.294', '0.0923', '-0.06866', '-0.6304', '-0.66', '-0.3113', '0.2976', '-0.1259', '0.0859', '0.3765', '0.00778', '-0.487', '0.178', '-0.0498', '0.1328', '0.2993', '0.5', '-0.7466', '0.2686', '-0.05127', '0.00852', '-0.062', '-0.1001', '-0.10767', '0.1593', '0.0802', '-0.07135', '-0.1594', '-0.51', '0.1904', '0.1974', '-0.02943', '0.798', '-0.2102', '0.3208', '-0.03284', '0.243', '-0.0879', '-0.04495', '0.147', '-0.04062', '0.1937', '0.1709', '0.586', '0.09894', '0.7017', '-0.3926', '0.5103', '0.269']",,0005834,C536053,733.99,,,
mondo:0010311,Becker muscular dystrophy,"['benign congenital myopathy', 'benign pseudohypertrophic muscular dystrophy', 'Becker dystrophinopathy', 'muscular dystrophy, Becker type', 'BMD', 'Becker muscular dystrophy, X-linked recessive', 'Becker^s muscular dystrophy', 'muscular dystrophy, pseudohypertrophic progressive, Becker type', 'Becker muscular dystrophy', 'muscular dystrophy pseudohypertrophic progressive, Becker type']",9883,300376,98895,C3490459,"['-0.02798', '-0.6284', '-0.588', '-0.2751', '0.4197', '-0.853', '0.786', '0.843', '-1.699', '-0.485', '0.2327', '0.4846', '-0.4495', '0.5454', '0.04242', '0.001317', '-0.867', '-0.4841', '-0.592', '-0.881', '0.5044', '-0.2157', '0.636', '0.3906', '-0.2773', '-0.266', '0.057', '-0.2673', '0.3022', '-0.3523', '0.7983', '0.1112', '0.514', '0.0722', '-0.01794', '-0.3157', '-0.1703', '0.014786', '-0.05548', '-0.173', '0.03232', '-0.2708', '-0.04498', '0.3672', '-0.3484', '0.3982', '-0.3538', '0.2308', '-0.0833', '0.4167', '-0.07715', '-0.2825', '0.1792', '-0.5684', '0.064', '-0.4316', '0.522', '0.686', '-0.1547', '-0.2037', '0.0897', '0.2423', '-0.0657', '0.2496', '-0.04816', '0.00961', '-0.1302', '0.1759', '-0.2424', '-0.102', '7.86e-05', '-0.02193', '-0.1417', '0.0669', '0.5225', '-0.04776', '-0.0839', '-0.2123', '0.0643', '0.0807', '0.4385', '-0.3257', '0.015495', '0.0729', '-0.0801', '0.4304', '-0.1037', '-0.5903', '0.523', '-0.1165', '-0.1715', '-0.3843', '-0.09155', '0.995', '0.1649', '-0.0003815', '0.55', '-0.454', '-0.2446', '0.3154']",C84587,,C570377,,,10059117,
mondo:0010312,"radial ray deficiency, X-linked","['radial ray deficiency', 'radial ray deficiency, X-linked', 'Rrdx']",,300378,,C1845717,,,,C564523,,,,
mondo:0010313,"intellectual disability, X-linked 63","['mental retardation, X-linked 68', 'mental retardation, X-linked 63', 'intellectual developmental disorder, X-linked 63, X-linked dominant', 'ACSL4 non-syndromic X-linked intellectual disability', 'mental retardation, X-linked type 63', 'intellectual disability, X-linked 63', 'MRX63', 'ACSL4-related intellectual disability', 'non-syndromic X-linked intellectual disability caused by mutation in ACSL4', 'intellectual disability, X-linked 68', 'intellectual disability, X-linked type 63']",0112050,300387,,C1845672,,,,C564522,,,,
mondo:0010314,"polymicrogyria, bilateral perisylvian, X-linked","['BPPX', 'polymicrogyria, bilateral perisylvian, X-linked dominant', 'polymicrogyria, bilateral perisylvian, X-linked', 'perisylvian syndrome, congenital bilateral', 'BPP', 'PMGX']",,300388,,,,,,,,,,
mondo:0010315,T-B+ severe combined immunodeficiency due to gamma chain deficiency,"['SCIDX', 'severe combined immunodeficiency, X-linked, X-linked recessive', 'X-linked SCID', 'severe combined immunodeficiency, X-linked', 'SCID, X-linked', 'SCID-X1', 'severe combined immunodeficiency T- B+ due to gamma chain deficiency', 'thymic epithelial hypoplasia', 'severe combined immunodeficiency T- B+, X-linked', 'X-SCID', 'T-B+ SCID due to gamma chain deficiency', 'severe combined immunodeficiency, X-linked, T cell-negative, B cell-positive, NK cell-negative', 'X-linked severe combined immunodeficiency', 'T-B+ severe combined immunodeficiency, X-linked', 'immunodeficiency 4', 'SCIDX1', 'T-B+ severe combined immunodeficiency due to gamma chain deficiency', 'XSCID']",0060013,300400,276,,"['-0.143', '0.1566', '0.06445', '-0.5156', '0.1746', '-0.3574', '0.1489', '0.4722', '0.51', '-0.1047', '0.1466', '-0.04834', '-0.64', '-0.0008254', '-0.4768', '-0.776', '0.2249', '-0.023', '-0.3765', '-0.772', '-0.4653', '-0.557', '1.166', '-0.191', '0.2124', '0.00567', '-0.3914', '0.1051', '-0.006527', '-0.4624', '0.265', '0.4304', '0.3938', '-0.2018', '-0.0098', '0.0753', '-0.4172', '-0.2039', '-0.603', '-0.1527', '-0.72', '-0.2235', '-0.0528', '-0.2617', '-0.5557', '-0.2603', '-0.35', '-0.9253', '0.083', '0.778', '0.1544', '-0.234', '0.02925', '-0.6235', '-0.3655', '0.3052', '0.0785', '-0.3896', '-0.12445', '0.2961', '-0.006054', '0.5815', '0.2908', '0.2493', '0.691', '-0.1764', '0.2966', '0.3254', '-0.5', '0.725', '-0.2294', '-0.03827', '-0.2124', '-0.149', '0.3005', '-0.33', '0.5117', '-0.3667', '-0.04984', '0.2161', '-0.1819', '-0.4817', '0.0646', '-0.1908', '-0.1134', '-0.604', '0.2041', '0.3376', '0.3926', '0.0784', '0.4277', '0.4517', '0.1707', '0.02141', '0.6865', '1.203', '-0.06445', '-1.107', '-0.1114', '-0.4907']",C4682,0005555,,,,,
mondo:0010316,FG syndrome 3,"['FGS3', 'FG syndrome 3']",,300406,,C1845567,,,,,,,,
mondo:0010317,"intellectual disability, X-linked, with or without seizures, arx-related","['intellectual disability, X-linked 33', 'MRX52', 'mental retardation, X-linked 33', 'mental retardation, X-linked 38', 'MRXARX', 'mental retardation, X-linked, with or without seizures, arx-related', 'mental retardation, X-linked 32', 'intellectual disability, X-linked 43', 'intellectual disability, X-linked 52', 'mental retardation, X-linked 87', 'intellectual disability, X-linked 87', 'intellectual developmental disorder, X-linked 29, X-linked recessive', 'intellectual disability, X-linked 54', 'intellectual disability, X-linked, with or without seizures, ARX-related', 'mental retardation, X-linked 52', 'ARX-related intellectual disability', 'intellectual disability, X-linked 29', 'mental retardation, X-linked 29', 'mental retardation, X-linked 76', 'mental retardation, X-linked, with or without seizures, arx-RELATED', 'mental retardation, X-linked 43', 'intellectual disability, X-linked 38', 'intellectual disability, X-linked 32', 'mental retardation, X-linked 54', 'intellectual disability, X-linked, with or without seizures, arx-RELATED', 'intellectual disability, X-linked 76']",0112021,300419,,C1845298,,,,C564502,,,,
mondo:0010318,FG syndrome 4,"['FG syndrome type 4', 'intellectual disability, X-linked, with or without Nystagmus', 'FG syndrome caused by mutation in cask', 'mental retardation, X-linked, with or without Nystagmus', 'FGS4', 'cask FG syndrome', 'mental retardation, with or without nystagmus', 'FG syndrome 4', 'X-linked intellectual disability with or without nystagmus', 'CASK FG syndrome']",,300422,,CN033933,"['-0.0334', '0.05493', '0.0144', '0.001219', '0.01426', '-0.05917', '0.002415', '0.06024', '-0.03745', '-0.032', '-0.02277', '0.01627', '0.013855', '0.004112', '-0.0227', '-0.04645', '-0.006794', '-0.02261', '-0.01784', '-0.0803', '-0.01619', '-0.01753', '0.05463', '-0.02385', '0.01788', '-0.004925', '-0.02623', '-0.01842', '0.01953', '-0.018', '0.04453', '-0.01487', '0.0633', '0.0253', '0.01595', '-0.03394', '-0.00459', '-0.02194', '0.003834', '-0.04446', '0.01563', '-0.05856', '0.02405', '-0.02585', '-0.004204', '-0.05896', '-0.02582', '0.04926', '0.00896', '0.01587', '-0.02269', '-0.01188', '-0.01729', '-0.00523', '-0.02687', '-0.02797', '0.0432', '-0.03616', '-0.0665', '0.01453', '0.03146', '0.03476', '0.003368', '0.01707', '0.006023', '-0.00981', '0.06494', '0.02393', '-0.03424', '0.06125', '-0.04196', '0.00886', '0.02411', '-0.04178', '0.01656', '0.02036', '-0.00586', '-0.00864', '-0.06012', '-0.03726', '0.0139', '0.00891', '-0.02472', '0.05768', '-0.0102', '-0.006447', '0.01862', '0.06696', '0.0717', '0.01409', '0.02692', '0.04416', '0.01182', '0.00247', '0.10974', '0.00978', '0.04376', '-0.0953', '-0.02155', '0.01678']",,,,,,,
mondo:0010319,syndromic X-linked intellectual disability Hedera type,"['intellectual disability, X-linked, with epilepsy', 'MRXE', 'X-linked intellectual disability with epilepsy', 'MRXSH', 'X-linked mental retardation with epilepsy', 'intellectual developmental disorder, X-linked, syndromic, Hedera type, X-linked recessive', 'intellectual disability, X-linked, syndromic, Hedera type', 'X-linked intellectual disability, Hedera type', 'mental retardation, X-linked, with epilepsy', 'mental retardation, X-linked, syndromic, Hedera type']",0060806,300423,93952,C1845543,"['-0.137', '0.11523', '0.1096', '-0.4526', '-0.1478', '-0.3809', '0.1943', '0.716', '-0.5596', '-0.0736', '-0.2303', '0.05225', '-0.09235', '0.0195', '0.2133', '0.09705', '0.384', '-0.0485', '-0.10016', '-0.3882', '0.1335', '0.1742', '-0.1699', '-0.002201', '0.1542', '-0.1355', '-0.2155', '-0.1857', '-0.011055', '-0.1658', '0.08514', '0.07416', '0.3538', '0.2106', '-0.0672', '-0.313', '-0.3318', '-0.3813', '-0.2362', '-0.2617', '0.04636', '-0.407', '-0.2654', '0.2837', '0.107', '-0.2734', '-0.11694', '0.2333', '-0.1624', '0.2673', '-0.05878', '0.3904', '-0.10815', '-0.1484', '0.02757', '-0.05862', '-0.01411', '-0.337', '-0.07495', '0.1054', '-0.075', '0.06946', '0.1853', '0.3188', '-0.2283', '0.1172', '0.0931', '0.45', '-0.1946', '0.1365', '-0.2952', '0.2072', '0.01671', '-0.355', '0.2139', '0.1449', '0.2013', '-0.155', '-0.08655', '0.01243', '0.0902', '-0.12085', '-0.03452', '0.4639', '0.2109', '0.3665', '-0.0542', '0.2822', '0.3584', '0.3833', '0.1434', '0.57', '-0.01921', '0.1187', '0.4792', '0.3276', '0.4048', '-0.143', '0.418', '0.09766']",,,C564516,,,,
mondo:0010320,retinitis pigmentosa 23,"['retinitis pigmentosa 23, X-linked recessive', 'RP23', 'RP 23', 'retinitis pigmentosa 23', 'retinitis pigmentosa type 23', 'retinitis pigmentosa caused by mutation in OFD1', 'OFD1 retinitis pigmentosa']",0110412,300424,,C1419610,,,,,,H35.5,,
mondo:0010321,"autism, susceptibility to, X-linked 1","['susceptibility to X-linked autism 1', 'autism, susceptibility to, X-linked type 1', 'autism susceptibility, X-linked 1', 'AUTSX1', 'autism, susceptibility to, X-linked 1']",,300425,,,,,,,,,,
mondo:0010322,"intellectual disability, X-linked 2","['MRX2', 'mental retardation, X-linked 2', 'intellectual disability, X-linked 2']",0112016,300428,,C0796207,,,,C563135,,,,
mondo:0010323,Atkin-Flaitz syndrome,"['Atkin-Flaitz syndrome', 'X-linked intellectual disability, Atkin type', 'Atkin syndrome']",,300431,1193,,,,,,,,,
mondo:0010324,"intellectual disability, X-linked 81","['MRX81', 'intellectual disability, X-linked 81', 'mental retardation, X-linked 81, X-linked recessive', 'mental retardation, X-linked 81']",0112033,300433,,C1845531,,,,C564515,,,,
mondo:0010325,"X-linked intellectual disability, Stocco dos Santos type","['Stocco DOS Santos X-linked intellectual disability syndrome', 'Stocco DOS Santos X-linked mental retardation syndrome', 'Stocco dos Santos syndrome', 'mental retardation, Stocco dos Santos type', 'intellectual developmental disorder, X-linked syndromic, Stocco dos Santos type', 'Sdsx', 'intellectual disability, Stocco dos Santos type', 'intellectual disability, X-linked, Stocco Dos Santos type', 'mental retardation, X-linked, Stocco Dos Santos type', 'SDSX']",0112126,300434,85288,C1845530,"['-0.391', '0.2664', '0.363', '-0.3838', '0.1948', '-0.6396', '0.2087', '0.2473', '-0.3835', '-0.45', '-0.1032', '0.1199', '0.0953', '-0.03143', '0.1605', '0.1819', '0.1134', '-0.1378', '-0.4475', '-0.3547', '0.0711', '0.2603', '0.2817', '-0.3623', '0.2744', '-0.27', '-0.02275', '-0.4485', '0.2047', '-0.3643', '0.1239', '-0.1332', '0.236', '0.174', '0.10187', '-0.185', '-0.10095', '-0.6147', '-0.459', '-0.1934', '0.0898', '-0.4133', '0.0479', '0.10736', '-0.1896', '-0.0987', '-0.005688', '-0.03333', '-0.2235', '0.1556', '-0.2216', '0.002981', '-0.01799', '-0.0932', '0.1084', '-0.1464', '0.3464', '-0.2795', '0.1055', '0.5615', '-0.02185', '-0.02107', '0.06097', '0.361', '0.0981', '-0.11707', '0.1144', '0.1454', '-0.5293', '0.01305', '-0.202', '-0.0717', '-0.218', '-0.3293', '-0.1417', '0.01714', '0.06683', '-0.05075', '-0.1793', '0.1438', '0.2832', '0.3027', '-0.312', '0.5684', '-0.02637', '0.1755', '-0.01058', '0.589', '0.2013', '0.4265', '-0.3567', '0.5728', '0.1699', '-0.1917', '0.4678', '0.2573', '0.305', '-0.7837', '0.3518', '-0.02205']",,,C537495,,,,
mondo:0010326,"intellectual disability, X-linked 46","['intellectual disability, X-linked 46', 'non-syndromic X-linked intellectual disability caused by mutation in ARHGEF6', 'mental retardation, X-linked 46', 'mental retardation, X-linked 46, X-linked recessive', 'intellectual disability, X-linked type 46', 'MRX46', 'mental retardation, X-linked type 46', 'ARHGEF6 non-syndromic X-linked intellectual disability']",0112055,300436,,C1845526,,,,C564513,,,,
mondo:0010327,HSD10 mitochondrial disease,"['2M3HBA', 'MHBD deficiency', 'mental retardation with chorioathetosis and abnormal behavior', 'HSD10MD', 'chorioathetosis with mental retardation and abnormal behaviour', 'HSD10 deficiency', '2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency', 'HSD10 deficiency, atypical type', 'HSD10 mitochondrial disease', 'mental retardation, X-linked, syndromic 10', 'chorioathetosis with mental retardation and abnormal behavior', '17-beta-hydroxysteroid dehydrogenase X deficiency', '17 beta-hydroxysteroid dehydrogenase type 10 deficiency', '3-hydroxy-2-methylbutyryl-CoA dehydrogenase deficiency', 'MRXS10', 'X-linked intellectual disability-choreoathetosis-abnormal behaviour syndrome', 'mental retardation, X-linked syndromic 10', '17-beta-hydroxysteroid dehydrogenase 10 deficiency', 'HSD10 mitochondrial disease, X-linked dominant', 'hydroxyacyl-CoA dehydrogenase II deficiency', '3H2MBD deficiency', 'mental retardation with chorioathetosis and abnormal behaviour', '3-hydroxyacyl-CoA dehydrogenase 2 deficiency', 'HSD17B10 deficiency', 'X-linked intellectual disability-choreoathetosis-abnormal behavior syndrome', 'mental retardation, X-linked, syndromic type 10', 'syndromic X-linked intellectual disability type 10', '2-methyl-3-hydroxybutyric aciduria']",0060810,300438,85295,CN204973,"['-0.2886', '0.2222', '-0.1398', '0.1812', '0.3652', '-0.938', '-0.3428', '0.568', '-0.399', '0.01401', '-0.532', '-0.713', '-0.1506', '0.33', '0.4182', '-0.3682', '0.0856', '-0.03516', '-0.4854', '-0.963', '0.035', '-0.4346', '0.4534', '-0.2424', '0.1372', '-0.3928', '0.1523', '-0.11865', '-0.507', '0.88', '0.786', '-0.02751', '0.628', '0.4043', '-0.2084', '-0.3398', '-0.9336', '-0.1273', '0.0609', '0.4258', '0.4514', '-0.5273', '0.6377', '-0.03088', '0.04807', '-0.3547', '-0.0647', '-0.2322', '-0.4587', '0.5347', '-0.06165', '0.372', '-0.2279', '-0.523', '0.647', '-0.11194', '0.2869', '-0.03845', '0.03099', '0.306', '0.00972', '-0.1527', '0.5283', '-0.0907', '-0.4565', '-0.275', '0.413', '0.02707', '-0.575', '0.274', '0.1277', '0.2554', '-0.226', '0.2219', '0.3723', '0.0779', '0.2286', '0.04938', '-0.5723', '0.2106', '0.1553', '-0.3704', '-0.08386', '-0.1533', '0.34', '0.549', '-0.345', '-0.1266', '0.4194', '0.588', '0.713', '0.3792', '-0.2211', '-0.04407', '0.3308', '0.625', '0.6177', '0.04807', '0.1422', '0.1284']",,,C564560,,,,
mondo:0010328,alpha-thalassemia-myelodysplastic syndrome,"['ALPHA-thalassemia myelodysplasia syndrome', 'acquired hemoglobin H disease', 'Haemoglobin H disease, acquired', 'Hemoglobin H disease, acquired', 'acquired HbH disease', 'ATMDS', 'acquired haemoglobin H disease', 'alpha-thalassemia myelodysplasia syndrome, somatic']",0112125,300448,231401,C0585216,"['-0.3323', '0.1854', '-0.2046', '-0.539', '-0.01106', '-0.4512', '-0.698', '1.303', '-0.8623', '-0.8535', '-0.1652', '0.10236', '0.039', '0.625', '-0.1711', '-0.0861', '-1.644', '-0.234', '-0.536', '-0.626', '-0.4458', '-0.2144', '0.9966', '-0.699', '0.564', '-0.3203', '0.5093', '-0.3506', '0.4429', '-0.723', '-0.05203', '-0.1525', '-0.08215', '-0.588', '-0.2067', '-0.6553', '-0.888', '-0.03873', '-0.306', '-0.822', '0.01791', '0.5176', '0.2515', '-0.2439', '-0.356', '-0.594', '-1.161', '-0.5767', '0.369', '-0.8994', '0.3003', '-0.5293', '0.2812', '0.1936', '-0.06836', '0.4475', '-0.4705', '0.703', '-0.0761', '0.345', '-0.4355', '0.0339', '-0.3271', '-0.3599', '-0.3582', '0.1218', '0.1215', '0.4666', '-1.252', '0.986', '0.0209', '0.1741', '-0.05844', '0.003462', '0.6055', '0.0799', '-0.1139', '0.1237', '0.1516', '0.0564', '-0.1846', '-0.7544', '0.12244', '-0.2507', '-0.274', '0.008736', '0.2742', '0.206', '0.006886', '0.327', '0.2458', '-0.1891', '-0.2563', '-0.1509', '0.564', '0.4258', '-0.283', '-0.452', '-0.3647', '-0.817']",,,C563023,282.49,D56.0,,
mondo:0010329,"intellectual disability, X-linked 77","['intellectual disability, X-linked 77', 'mental retardation, X-linked 77, X-linked recessive', 'mental retardation, X-linked 77', 'MRX77']",0112039,300454,,C1845499,,,,C564511,,,,
mondo:0010331,"coronary heart disease, susceptibility to, 3","['Chds3', 'coronary heart disease, susceptibility to, 3', 'coronary heart disease, susceptibility to, type 3']",,300464,,,,,,,,,,
mondo:0010332,X-linked intellectual disability-cubitus valgus-dysmorphism syndrome,"['Cubitus valgus with mental retardation and unusual facies, X-linked recessive', 'cubitus valgus with intellectual disability and unusual facies', 'cubitus valgus with mental retardation and unusual facies']",,300471,85280,C1845450,,,,C564510,,,,
mondo:0010333,corpus callosum agenesis-intellectual disability-coloboma-micrognathia syndrome,"['corpus callosum, agenesis of, with intellectual disability, ocular coloboma, and micrognathia', 'corpus callosum, agenesis of, with mental retardation, ocular coloboma, and micrognathia', 'corpus callosum, agenesis of, with impaired intellectual development, ocular coloboma and micrognathia, X-linked recessive', 'agenesis of the corpus callosum-intellectual disability-coloboma-micrognathia syndrome', 'corpus callosum, agenesis of, with intellectual disability, ocular coloboma and micrognathia', 'corpus callosum, agenesis of, with mental retardation, ocular coloboma and micrognathia', 'Graham-Cox syndrome', 'intellectual disability, X-linked, syndromic 28', 'mental retardation, X-linked, syndromic 28', 'MRXS28']",0060816,300472,52055,,"['-0.2646', '0.4329', '0.809', '-0.405', '0.1987', '-0.1931', '0.2179', '0.736', '-0.2546', '-0.3425', '-0.2291', '-0.5205', '-0.1248', '-0.4597', '-0.622', '-0.2319', '0.4294', '-0.2773', '-0.3838', '-0.5024', '0.4468', '-0.1539', '-0.197', '0.2393', '0.4417', '0.11365', '-0.446', '0.124', '0.4753', '-0.1952', '0.272', '-0.08655', '0.5835', '0.0756', '0.1699', '-0.0903', '0.10535', '-0.4856', '-0.12494', '-0.7134', '0.0916', '-0.1243', '0.1685', '-0.3342', '0.04788', '-0.4932', '0.327', '0.2534', '0.2834', '-0.2852', '-0.1575', '0.11194', '-0.269', '-0.1628', '-0.4023', '-0.2515', '0.0802', '-0.1224', '-0.3525', '0.2433', '-0.309', '0.0383', '-0.1483', '0.1271', '-0.532', '0.2664', '0.08856', '0.616', '-0.648', '0.2551', '-0.3098', '0.4907', '0.4285', '-0.2534', '-0.2722', '-0.101', '0.5386', '0.0793', '-0.3716', '-0.03168', '0.2367', '0.0863', '-0.0905', '0.921', '-0.263', '-0.1076', '0.0185', '0.896', '-2.9e-06', '0.6597', '0.1296', '0.8223', '0.3833', '-0.08887', '0.995', '-0.315', '0.6265', '-0.449', '0.5566', '0.643']",,,C564509,,,,
mondo:0010334,severe motor and intellectual disabilities-sensorineural deafness-dystonia syndrome,"['DDCH', 'deafness, dystonia, and cerebral hypomyelination', 'deafness, dystonia, and cerebral hypomyelination, X-linked recessive', 'contiguous ABCD1/Dxs1375E deletion syndrome']",0112123,300475,369939,CN204816,"['0.4683', '0.1741', '0.3083', '-0.2917', '-0.24', '-0.898', '-0.126', '0.1923', '-0.965', '0.08264', '1.104', '0.5083', '-0.4734', '-0.06198', '0.1812', '0.4612', '0.1141', '-0.545', '-0.642', '-0.8267', '-0.1567', '-0.12177', '-0.403', '-0.4148', '-0.2722', '0.1521', '-0.0743', '-0.0213', '-0.2109', '-0.1458', '0.1567', '0.622', '1.402', '-0.3657', '0.353', '0.10876', '0.1854', '-0.02957', '0.462', '-0.3025', '0.657', '0.1476', '-0.612', '0.4434', '0.33', '-0.199', '-0.2202', '0.3635', '0.4868', '-0.1525', '0.152', '0.1973', '0.329', '0.1422', '0.46', '-0.1973', '-0.132', '0.5425', '-0.2585', '0.1586', '-0.9995', '-0.6094', '-0.07043', '-0.2646', '-0.9434', '0.5063', '0.34', '0.801', '-0.3088', '0.578', '-0.4673', '0.2615', '0.01077', '-0.07306', '-0.04337', '0.2908', '1.187', '-0.1405', '0.1164', '-0.1539', '0.09155', '0.403', '0.2274', '0.507', '0.906', '-0.0684', '-0.1046', '0.525', '1.547', '0.3945', '0.42', '0.7227', '0.7627', '0.4268', '0.7524', '-0.2605', '-0.594', '0.09143', '0.763', '-0.2512']",,,C564508,,,,
mondo:0010335,X-linked cone-rod dystrophy 3,"['cone-rod dystrophy, X-linked, 3', 'cone-rod dystrophy X-linked 3', 'cone-rod dystrophy, X-linked, type 3', 'CORDX3', 'cone-rod dystrophy, X-linked, 3, X-linked recessive', 'X-linked cone-rod dystrophy type 3']",0111007,300476,,,,,,C564507,,,,
mondo:0010336,orofaciodigital syndrome VIII,"['orofaciodigital syndrome type VIII', 'oral-facial-digital syndrome, Edwards type', 'oral-Facial-digital syndrome with hypoplastic Epiglottis', 'oral facial digital syndrome type 8', 'oral-Facial-digital syndrome, type 8', 'OFD syndrome 8', 'orofaciodigital syndrome VIII', 'Ofds 8', 'orofaciodigital syndrome 8', 'oral facial digital syndrome 8', 'orofaciodigital syndrome type 8', 'oral-facial-digital syndrome type 8', 'OFD8', 'orofaciodigital syndrome VIII, X-linked recessive', 'orofaciodigital syndrome, Edwards type']",0060378,300484,2755,C0152096,,,,C557820,,,,
mondo:0010337,X-linked intellectual disability-cerebellar hypoplasia syndrome,"['OPHN1 XLMR', 'intellectual disability, X-linked 60, formerly', 'intellectual developmental disorder, X-linked syndromic, Billuart type, X-linked recessive', 'OPHN1- related XLID', 'MRX60 (formerly)', 'intellectual disability, X-linked, with cerebellar hypoplasia and distinctive facial appearance', 'mental retardation, X-linked 60', 'intellectual disability X-linked with cerebellar hypoplasia and distinctive facial appearance', 'mental retardation X-linked 60 (formerly)', 'X-linked intellectual Deficit with cerebellar Hypoplasia', 'mental retardation X-linked with cerebellar hypoplasia and distinctive facial appearance', 'intellectual disability X-linked 60 (formerly)', 'OPHN1 deficiency', 'mental retardation, X-linked 60, formerly', 'OPHN1 XLMR, X-linked intellectual disability', 'mental retardation, X-linked, with cerebellar hypoplasia and distinctive facial appearance', 'intellectual disability, X-linked 60', 'OPHN1 syndrome', 'Oligophrenin-1 syndrome']",0080311,300486,137831,,"['-0.01493', '0.2018', '0.2286', '-0.418', '0.1355', '-0.7173', '0.1052', '0.7515', '-0.2761', '-0.509', '0.449', '-0.3308', '-0.1826', '-0.512', '0.4038', '0.07764', '0.5684', '-0.1782', '0.076', '-0.568', '0.12494', '0.372', '-0.05038', '-0.0795', '-0.0978', '-0.311', '-0.422', '-0.2041', '0.6743', '-0.2798', '0.395', '-0.2593', '0.7183', '-0.07306', '-0.069', '-0.1952', '-0.2554', '-0.3582', '-0.4165', '-0.274', '0.4448', '-0.5903', '0.1582', '0.0737', '0.1406', '-0.2737', '-0.3108', '-0.06305', '-0.1888', '-0.0902', '-0.4202', '0.0619', '-0.475', '0.2737', '-0.4597', '0.2361', '0.6787', '-0.2627', '-0.07446', '0.563', '-0.1085', '-0.092', '0.2169', '0.7295', '-0.549', '-0.1342', '0.1542', '0.3962', '-0.3987', '0.3923', '-0.197', '0.62', '0.2832', '0.4526', '-0.1497', '0.4543', '0.5513', '-0.4875', '-0.4438', '0.737', '-0.0729', '0.1666', '0.2896', '0.316', '0.485', '0.0952', '-0.2317', '0.691', '0.2195', '0.7744', '-0.1259', '1.108', '0.02821', '0.274', '0.975', '0.5625', '0.0264', '-0.3542', '0.8926', '0.0063']",,,C537456,,,,
mondo:0010338,X-linked distal spinal muscular atrophy type 3,"['spinal muscular atrophy, distal, X-linked type 3', 'X-linked dHMN3', 'Dsmax', 'ATP7A-related distal motor neuropathy', 'X-linked dSMA3', 'spinal muscular atrophy caused by mutation in ATP7A', 'spinal muscular atrophy, distal, X-linked recessive', 'X-linked distal hereditary motor neuropathy type 3', 'X-linked dHMN type 3', 'ATP7A spinal muscular atrophy', 'spinal muscular atrophy, distal, X-linked 3', 'X-linked dSMA type 3', 'SMAX3', 'DSMAX', 'spinal muscular atrophy, distal, X-linked 3, X-linked recessive']",0111196,300489,139557,C1845359,"['-0.4705', '-0.06696', '0.2742', '-0.331', '0.07495', '-0.584', '-0.1445', '0.8857', '-0.8037', '-0.05316', '-0.006554', '-0.02605', '-0.4443', '0.198', '0.4224', '0.1704', '0.386', '-0.5107', '-0.0739', '-0.6436', '-0.145', '-0.328', '0.1692', '0.3735', '-0.1312', '0.03967', '0.00408', '-0.0673', '-0.4495', '-0.08936', '0.0791', '-0.2507', '0.0652', '0.317', '0.01657', '-0.656', '-0.1642', '0.02359', '0.03943', '-0.1279', '-0.6', '-0.62', '-0.407', '0.3704', '-0.3162', '-0.2498', '-0.2102', '0.551', '0.02454', '0.05563', '-0.1697', '0.3005', '-0.10315', '-0.4595', '-0.2374', '-0.4097', '0.364', '-0.317', '-0.3374', '-0.00593', '-0.3948', '-0.536', '0.142', '0.451', '-0.873', '0.2898', '0.2314', '0.941', '-0.3484', '0.1594', '-0.4097', '0.05026', '0.001181', '-0.3108', '0.6553', '0.3628', '0.1301', '0.4834', '-0.186', '-0.2009', '-0.3147', '-0.4048', '0.6113', '0.599', '-0.208', '0.08704', '-0.221', '0.2167', '0.1432', '0.07587', '0.3044', '0.2705', '0.2263', '0.1635', '0.584', '0.1284', '0.4404', '-0.525', '-0.092', '0.4658']",,,C564506,,,,
mondo:0010339,"epilepsy, X-linked 1, with variable learning disabilities and behavior disorders","['X-linked epilepsy-learning disabilities-behavior disorders syndrome', 'epilepsy, X-linked, with variable learning disabilities and behaviour disorders, X-linked recessive, X-linked dominant', 'epilepsy, X-linked, with variable learning disabilities and behavior disorders, X-linked recessive, X-linked dominant', 'epilepsy, X-linked, with variable learning disabilities and behaviour disorders', 'epilepsy, X-linked, with variable learning disabilities and behavior disorders']",0112122,300491,85294,C1845343,"['1.025', '0.1914', '-0.1443', '-0.1425', '-0.3074', '-0.3352', '0.697', '0.1926', '-0.572', '-0.4304', '0.1532', '-0.1644', '-0.3904', '0.3604', '0.1412', '0.01371', '-0.2406', '-0.3818', '-0.5415', '-0.674', '-0.2393', '0.7495', '0.08014', '-0.523', '-0.2808', '-0.06573', '-0.1456', '-0.1192', '-0.3384', '0.3606', '0.2205', '-0.624', '0.2964', '0.0876', '0.7954', '0.3662', '-0.1572', '-0.12', '-0.00417', '-0.4404', '-0.197', '-0.2993', '0.02074', '-0.1857', '-0.4143', '-0.7554', '0.04446', '0.1431', '0.7544', '0.5967', '-0.3347', '0.3', '-0.01445', '-0.3733', '0.204', '-0.1068', '-0.05542', '0.1276', '-0.2327', '0.4224', '-0.823', '0.606', '0.7456', '-0.12335', '-0.3386', '1.295', '0.1152', '-0.00405', '-1.001', '0.738', '0.9575', '1.004', '-0.11865', '-0.1967', '0.208', '0.8325', '0.8726', '0.57', '-0.3892', '0.3857', '-0.191', '0.748', '0.4028', '0.4014', '0.3293', '0.1942', '0.1481', '0.682', '0.7183', '0.4968', '-0.1906', '0.0324', '-0.269', '0.1738', '0.257', '0.2673', '0.3442', '-0.7075', '0.2688', '0.3706']",,,C564505,,,,
mondo:0010340,"Asperger syndrome, X-linked, susceptibility to, 1","['ASPERGER syndrome, X-linked, susceptibility to, 1', 'ASPGX1', 'Asperger syndrome, X-linked, susceptibility to, 1', 'Asperger syndrome susceptibility, X-linked 1, Isolated cases, X-linked', 'Asperger syndrome, X-linked, susceptibility to, type 1', 'susceptibility to X-linked asperger syndrome 1']",,300494,,C1845341,,,,,,,,
mondo:0010341,"autism, susceptibility to, X-linked 2","['mental retardation, X-linked', 'intellectual developmental disorder, X-linked, Isolated cases, X-linked', 'susceptibility to X-linked autism 2', 'AUTSX2', 'autism, susceptibility to, X-linked type 2', 'autism susceptibility, X-linked 2, isolated cases, X-linked', 'autism, susceptibility to, X-linked 2', 'intellectual disability, X-linked']",,300495,,,,,,D038901,,,,
mondo:0010342,"autism, susceptibility to, X-linked 3","['autism, susceptibility to, X-linked 3', 'AUTSX3', 'autism, susceptibility to, X-linked type 3', 'susceptibility to X-linked autism 3', 'autism susceptibility, X-linked 3']",,300496,,,,,,,,,,
mondo:0010343,"Asperger syndrome, X-linked, susceptibility to, 2","['ASPERGER syndrome, X-linked, susceptibility to, 2', 'Asperger syndrome, X-linked, susceptibility to, type 2', 'Asperger syndrome, X-linked, susceptibility to, 2', 'susceptibility to X-linked asperger syndrome 2', 'ASPGX2', 'Asperger syndrome susceptibility, X-linked 2']",,300497,,,,,,,,,,
mondo:0010344,"intellectual disability, X-linked 45","['mental retardation, X-linked 45', 'ZNF81 non-syndromic X-linked intellectual disability', 'mental retardation, X-linked type 45', 'non-syndromic X-linked intellectual disability caused by mutation in ZNF81', 'intellectual disability, X-linked 45', 'MRX45', 'intellectual disability, X-linked type 45']",0112028,300498,,C1845333,,,,C564503,,,,
mondo:0010347,"intellectual disability, X-linked 84","['intellectual disability, X-linked 84', 'mental retardation, X-linked 84, X-linked recessive', 'mental retardation, X-linked 84', 'MRX84']",0112030,300505,,C1845297,,,,C564501,,,,
mondo:0010348,"dyslexia, susceptibility to, 9","['dyslexia, susceptibility to, 9', 'DYX9']",,300509,,,,,,,,,,
mondo:0010349,ovarian dysgenesis 2,"['ovarian dysgenesis type 2', 'ODG2', 'ovarian failure, hypergonadotropic, due to ovarian dysgenesis', 'premature ovarian failure 4', 'ovarian dysgenesis 2', 'ovarian dysgenesis, hypergonadotropic, X-linked', 'primary ovarian failure caused by mutation in BMP15', 'BMP15 primary ovarian failure']",0080861,300510,,C1845294,,,,C564499,,,,
mondo:0010350,premature ovarian failure 2A,"['premature ovarian failure 2A, X-linked dominant', 'primary ovarian failure caused by mutation in DIAPH2', 'premature ovarian failure type 2A', 'premature ovarian failure 2A', 'POF2A', 'DIAPH2 primary ovarian failure']",0080858,300511,,C1845293,,,,C564498,,,,
mondo:0010351,Fanconi anemia complementation group B,"['Fanconi pancytopenia type 2', 'FA2', 'FACB', 'Fanconi pancytopenia, type 2', 'Fanconi anemia, complementation group B, X-linked recessive', 'Fanconi anaemia complementation group type B', 'Fanconi Anemia, complementation group type B', 'Fanconi anemia complementation group type B', 'Fanconi anemia, complementation group B', 'FANCB']",0111098,300514,,C1845292,,C125703,,C564497,,,,
mondo:0010352,"intellectual disability, X-linked 82","['mental retardation, X-linked 82, X-linked recessive', 'MRX82', 'intellectual disability, X-linked 82', 'mental retardation, X-linked 82']",0112052,300518,,C1845286,,,,C564496,,,,
mondo:0010353,"deafness-intellectual disability, Martin-Probst type syndrome","['Martin-Probst deafness-mental retardation syndrome', 'martin-probst syndrome, X-linked recessive', 'Martin-Probst syndrome', 'intellectual disability, X-linked, syndromic, Martin-Probst type', 'deafness-intellectual disability syndrome, Martin-Probst type', 'mental retardation, X-linked, syndromic, Martin-Probst type', 'intellectual disability, X-linked, syndromic, MARTIN-Probst type', 'mental retardation, X-linked, syndromic, MARTIN-Probst type', 'X-linked deafness-intellectual disability syndrome syndrome', 'Martin-Probst deafness-intellectual disability syndrome', 'MRXSMP']",0060830,300519,85321,,"['-0.2142', '0.5146', '0.02705', '-0.5776', '0.2023', '-0.593', '0.11334', '0.6343', '-0.4028', '-0.2964', '-0.2148', '-0.2534', '-0.10736', '0.2024', '-0.4233', '-0.00125', '0.356', '-0.056', '-0.4739', '-0.3154', '0.1884', '-0.1244', '0.3208', '-0.3535', '0.739', '-0.3489', '-0.4932', '0.04388', '0.537', '-0.752', '0.871', '-0.1565', '0.1456', '0.1301', '0.211', '-0.642', '-0.5283', '-0.681', '-0.00392', '-0.4102', '0.2269', '0.04257', '0.118', '-0.132', '-0.0416', '-0.3975', '0.1859', '-0.2944', '-0.7104', '-0.473', '-0.0415', '-0.0638', '-0.1642', '0.06824', '-0.02492', '-0.6978', '0.3608', '0.10925', '-0.1991', '0.5605', '-0.1266', '-0.2141', '-0.349', '0.4749', '-0.1444', '-0.1659', '0.2106', '0.511', '-0.5903', '0.3645', '-0.46', '-0.0441', '0.1985', '-0.2157', '-0.2433', '-0.01959', '0.4045', '-0.11566', '-0.02539', '0.3574', '-0.01309', '0.3086', '0.11505', '0.4568', '-3.87e-05', '-0.07983', '0.2073', '0.3008', '-0.03696', '0.1312', '-0.3262', '0.9956', '0.5557', '-0.2522', '1.234', '-0.1652', '0.2837', '-0.5786', '0.5596', '-0.1428']",,,C564495,,,,
mondo:0010354,Allan-Herndon-Dudley syndrome,"['mental retardation, X-linked, with hypotonia', 'X-linked intellectual disability-hypotonia syndrome', 'triiodothyronine resistence', 'MCT8 deficiency', 'AHDS', 'Allan-Herndon-Dudley syndrome', 'ALLAN-Herndon-DUDLEY syndrome', 'T3 resisitence', 'ALLAN-Herndon syndrome', 'Allan-Herndon syndrome', 'intellectual disability and muscular atrophy', 'T3 resistance', 'monocarboxylate transporter 8 deficiency', 'X-linked intellectual disability with hypotonia', 'intellectual disability, X-linked, with hypotonia', 'triiodothyronine resistance', 'monocarboxylate transporter-8 deficiency', 'mental retardation and muscular atrophy', 'MCT8-specific thyroid hormone cell Membrane transporter deficiency']",0050631,300523,59,C0795889,"['0.1547', '0.1608', '-0.0553', '-0.304', '-0.3003', '-0.3342', '0.07806', '0.941', '-1.1875', '-0.7993', '0.1823', '-0.3145', '0.04004', '-0.0977', '0.1019', '0.486', '0.2236', '-0.527', '0.0712', '-1.032', '0.3127', '-0.4436', '0.07135', '-0.3882', '-0.1493', '-0.3613', '-0.1768', '-0.07184', '-0.07324', '-0.0871', '0.615', '0.01959', '0.3467', '0.4126', '-0.4775', '-0.3323', '0.35', '-0.4326', '-0.2585', '-0.03336', '0.151', '-0.5127', '-0.6836', '0.287', '0.4329', '0.3894', '0.2211', '0.2347', '0.2148', '0.02007', '-1.117', '0.1161', '0.1149', '-0.03693', '-0.0933', '-0.317', '0.5894', '0.2517', '0.0563', '0.1654', '-0.5024', '0.02327', '-0.128', '0.421', '-0.0532', '0.00555', '0.11566', '0.0733', '0.01698', '0.2808', '-0.4446', '0.0862', '-0.1272', '0.01765', '0.6006', '0.1395', '0.1033', '-0.4287', '-0.3545', '0.1633', '0.1619', '0.07117', '0.02184', '0.0739', '0.05237', '0.422', '-0.1309', '0.6104', '0.3047', '0.4182', '0.67', '0.1953', '-0.01519', '0.02162', '0.3625', '0.04715', '0.1865', '-0.05234', '0.6973', '-0.652']",C118843,,C537047,,,,
mondo:0010355,syndromic X-linked intellectual disability Claes-Jensen type,"['syndromic X-linked intellectual disability due to JARID1C mutation', 'intellectual disability, X-linked, syndromic, Claes-Jensen type', 'intellectual disability, X-linked, syndromic, JARID1C-related', 'mental retardation, X-linked, syndromic, JARID1C-related', 'syndromic X-linked intellectual disability JARID1C-related', 'intellectual developmental disorder, X-linked syndromic, Claes-Jensen type, X-linked recessive', 'syndromic X-linked mental retardation JARID1C-related', 'mental retardation, X-linked, syndromic, Claes-Jensen type', 'MRXSCJ', 'MRXSJ']",0060809,300534,85279,C4304915,"['-0.3474', '0.497', '0.5215', '-0.613', '0.254', '-0.6055', '0.0731', '0.504', '-0.3057', '-0.5796', '-0.003754', '-0.08264', '-0.0738', '-0.554', '0.4182', '0.2338', '0.4075', '-0.3533', '-0.679', '-0.3472', '0.2151', '0.1932', '0.0738', '-0.3945', '0.0963', '-0.0679', '-0.0901', '-0.2369', '0.04257', '-0.2715', '0.00888', '-0.0689', '0.6025', '0.0077', '0.2427', '-0.666', '-0.1122', '-0.3372', '-0.3127', '-0.2091', '0.2917', '-0.19', '-0.00628', '-0.1354', '0.02597', '-0.641', '0.078', '-0.2751', '-0.013435', '-0.2915', '-0.3003', '0.0536', '-0.2072', '0.1357', '0.116', '0.05554', '0.545', '-0.289', '-0.03336', '0.2329', '-0.05075', '0.399', '0.1643', '0.0544', '0.2096', '-0.0561', '-0.1001', '0.434', '-0.4636', '-0.07556', '-0.1989', '0.3174', '-0.03375', '-0.0431', '-0.006367', '0.3909', '0.3457', '-0.0951', '-0.1228', '0.4229', '0.4219', '0.2205', '0.0627', '0.509', '0.2332', '0.5786', '0.03674', '0.638', '0.323', '0.647', '0.09314', '0.6323', '-0.2957', '-0.1406', '1.067', '0.307', '0.267', '-0.552', '0.626', '0.12494']",,,C564494,,,,
mondo:0010356,nephrogenic syndrome of inappropriate antidiuresis,"['nephrogenic syndrome of inappropriate antidiuresis', 'nephrogenic syndrome of inappropriate antidiuresis, X-linked recessive', 'NSIAD']",0112121,300539,93606,C1845202,"['-0.1932', '0.2507', '-0.3047', '0.1652', '-0.1688', '0.087', '0.3276', '0.618', '0.0827', '-0.341', '-0.1165', '-0.05783', '0.1671', '0.5493', '-0.05078', '0.1362', '0.1813', '0.1635', '0.071', '-0.4312', '-0.372', '-0.283', '0.5225', '-0.3184', '0.2157', '-0.486', '-0.1921', '0.07446', '-0.4575', '-0.3894', '0.516', '0.08234', '0.5493', '-0.1921', '-0.1877', '-0.177', '0.1946', '-0.1819', '0.06903', '-0.1255', '0.0946', '-0.384', '0.3088', '-0.819', '-0.0742', '0.0687', '-0.2003', '-0.099', '-0.4807', '0.8696', '-0.03854', '0.2937', '0.3066', '-0.2361', '0.0765', '0.2495', '0.5483', '-0.3306', '-0.1892', '0.4421', '0.2974', '0.975', '-0.07806', '-0.656', '0.1942', '0.138', '-0.06604', '0.04755', '-0.2512', '-0.1714', '-0.4934', '0.1377', '-0.0812', '0.1165', '0.6235', '0.1305', '-0.349', '0.689', '-0.102', '0.575', '-0.2006', '0.596', '0.506', '0.25', '0.2374', '0.3625', '-0.2417', '-0.3323', '0.4204', '-0.07544', '-0.02028', '0.558', '-0.71', '-0.2573', '0.4077', '0.509', '-0.05063', '-0.79', '0.225', '0.544']",,,C564491,,,,
mondo:0010358,"hypophosphatemic rickets, X-linked recessive","['hypophosphatemic rickets, X-linked recessive', 'CLCN5 X-linked hypophosphatemic rickets']",0080353,300554,93622,,,,,,,,,
mondo:0010359,Dent disease type 2,"['OCRL Dent disease', 'DENT disease 2', 'Dent disease caused by mutation in OCRL', 'nephrolithiasis type 2', 'Dent disease type 2', 'dent disease 2, X-linked recessive']",,300555,93623,C4305529,"['0.1554', '-0.05844', '0.1231', '-0.1813', '-0.2534', '-0.3938', '-0.2827', '1.024', '-0.3372', '-0.0672', '-0.24', '-0.221', '0.016', '0.4995', '0.1631', '-0.4656', '0.0844', '0.010254', '0.2598', '-0.412', '0.3933', '0.1181', '0.551', '-0.1857', '0.3157', '0.1816', '-0.145', '-0.3147', '0.3186', '-0.4365', '0.1693', '-0.4333', '0.553', '0.2363', '0.3398', '-0.5464', '-0.2717', '-0.4658', '-0.334', '0.732', '0.2249', '-0.1019', '0.0212', '0.0179', '-0.268', '0.1454', '-0.1588', '-0.1467', '-0.5483', '0.1048', '0.07404', '0.1606', '-0.1727', '-0.3416', '-0.4873', '-0.1348', '0.4846', '-0.3442', '-0.3972', '0.5986', '0.31', '-0.4187', '0.242', '0.0476', '0.05588', '0.2433', '-0.1671', '0.854', '-0.3523', '0.0653', '0.2786', '-0.1207', '0.12213', '-0.4072', '0.4836', '0.03598', '-0.3533', '-0.4946', '-0.471', '0.463', '-0.06027', '0.07623', '0.14', '0.3188', '-0.1919', '0.178', '0.3289', '0.288', '0.647', '0.2145', '0.541', '0.4165', '0.1832', '-0.1102', '0.5884', '0.05753', '0.02722', '-0.368', '0.1076', '0.1757']",,,C564487,,,,
mondo:0010360,parkinson disease 12,"['Parkinson disease, X-linked', 'PARK12', 'Parkinson disease 12']",,300557,,C1845165,,,,C564486,,,,
mondo:0010361,"intellectual disability, X-linked 30","['intellectual developmental disorder, X-linked 30, X-linked recessive', 'mental retardation, X-linked 30', 'mental retardation, X-linked 47', 'intellectual disability, X-linked 30', 'MRX30', 'PAK3 non-syndromic X-linked intellectual disability', 'non-syndromic X-linked intellectual disability caused by mutation in PAK3', 'intellectual disability, X-linked 47', 'mental retardation, X-linked type 30', 'intellectual disability, X-linked type 30']",0112051,300558,,C0796237,,,,,,,,
mondo:0010362,glycogen storage disease IXd,"['PHKA1 glycogen storage disease', 'glycogenosis type IXd', 'glycogen storage disease type IXd', 'glycogen storage disease, type IXd', 'GSD Vb', 'PHKA1-related glycogen storage disease type IX', 'GSD type 9D', 'GSD IXd', 'glycogen storage disease due to muscle phosphorylase kinase deficiency', 'muscle glycogenosis, X-linked recessive', 'glycogen storage disease type 9D', 'glycogenosis due to muscle phosphorylase kinase deficiency', 'muscle glycogenosis, X-linked', 'GSD due to muscle phosphorylase kinase deficiency', 'GSD type IXd', 'GSD9D', 'glycogen storage disease caused by mutation in PHKA1', 'glycogenosis type 9D', 'muscle phosphorylase kinase deficiency', 'muscular phosphorylase kinase deficiency']",0111040,300559,715,,"['-0.5615', '0.08795', '-0.4084', '0.1648', '0.0852', '-0.2247', '0.1837', '0.4895', '-0.319', '0.08075', '-0.3242', '0.05228', '-0.1921', '0.2462', '-0.12256', '0.4001', '-0.02643', '-0.2014', '-1.193', '-0.5435', '0.4055', '-0.521', '0.8574', '0.4065', '-0.368', '-0.1438', '0.04388', '-0.5376', '0.02023', '0.2676', '0.578', '-0.147', '0.2598', '0.2279', '-0.1484', '-0.4084', '-0.4707', '0.4167', '0.2563', '0.6367', '0.54', '-0.4941', '-0.06964', '0.495', '-0.456', '-0.245', '-0.03595', '-0.2876', '-0.446', '0.603', '0.08594', '-0.3489', '0.01457', '0.407', '0.1693', '-1.072', '0.476', '-0.0861', '-0.03995', '0.1658', '0.2632', '0.02237', '0.1909', '-0.2178', '-0.624', '0.1626', '0.6436', '0.2986', '-0.282', '0.2222', '0.2024', '-0.404', '0.2678', '0.591', '0.535', '0.5806', '-0.2937', '0.3066', '-0.1461', '0.2454', '0.617', '0.06635', '0.631', '-0.0434', '0.3496', '0.2264', '0.293', '0.3027', '0.79', '0.1996', '0.617', '0.104', '-0.1203', '-0.714', '1.129', '0.5654', '0.08887', '-0.4604', '-0.37', '0.0752']",,,C564485,,,,
mondo:0010363,"intellectual disability, X-linked 91","['intellectual disability, X-linked 91', 'mental retardation, X-linked 91, X-linked dominant', 'mental retardation, X-linked 91', 'mental retardation, X-linked type 91', 'non-syndromic X-linked intellectual disability caused by mutation in ZDHHC15', 'MRX91', 'intellectual disability, X-linked type 91', 'ZDHHC15 non-syndromic X-linked intellectual disability']",0112043,300577,,C1845142,,,,C564482,,,,
mondo:0010364,X-linked intellectual disability-retinitis pigmentosa syndrome,"['retinitis pigmentosa and intellectual disability due to monosomy Xp11.3', 'nonspecific mental retardation associated with retinitis pigmentosa', 'nonspecific intellectual disability associated with retinitis pigmentosa', 'mental retardation, X-linked, with retinitis pigmentosa', 'chromosome xp11.3 deletion syndrome, X-linked recessive', 'retinitis pigmentosa and intellectual disability due to del(X)(p11.3)', 'Aldred syndrome', 'X-linked mental handicap-retinitis pigmentosa syndrome', 'chromosome Xp11.3 deletion syndrome', 'intellectual disability, X-linked, with retinitis pigmentosa', 'retinitis pigmentosa and intellectual disability due to Xp11.3 microdeletion']",,300578,85332,C0795873,,,,,,H35.5,,
mondo:0010365,"myopathy, congenital, with fiber-type disproportion, X-linked","['CFTDX', 'myopathy, congenital, with fiber-type disproportion, X-linked', 'myopathy, congenital, with fiber-type disproportion, X-linked, X-linked dominant']",0111226,300580,,C2749128,,,,C567594,,,,
mondo:0010366,FG syndrome 5,"['FGS5', 'FG syndrome 5']",,300581,,C1845119,,,,C564480,,,,
mondo:0010367,SHOX-related short stature,"['short stature, idiopathic familial', 'short stature, idiopathic, X-linked', 'ISS']",0112120,300582,314795,,"['-0.292', '0.013916', '-0.1688', '-0.2125', '0.4343', '-0.2499', '0.1543', '1.177', '-0.7593', '-0.578', '0.2979', '0.3333', '0.02368', '0.807', '0.616', '0.11194', '0.5938', '-0.277', '-0.09283', '-0.6357', '-0.01846', '-0.1133', '0.656', '0.09985', '0.3425', '-0.03342', '0.1705', '0.1564', '-0.315', '0.1093', '0.3281', '-0.623', '-0.0338', '0.482', '0.11145', '0.2025', '-0.2217', '-0.2236', '-0.4475', '0.0774', '0.312', '-0.258', '-0.1848', '0.3882', '0.339', '-0.3901', '-0.0137', '0.3838', '0.0504', '0.1097', '0.1315', '-0.01266', '-0.4482', '-0.304', '-0.1768', '-0.2122', '-0.3357', '-0.42', '0.0248', '0.2212', '0.6104', '0.321', '-0.0807', '0.06635', '-0.2708', '0.1763', '-0.2449', '0.2925', '-0.1219', '0.09894', '-0.0865', '0.1116', '0.2249', '-0.589', '0.596', '-0.06256', '-0.2856', '-0.1979', '-0.577', '-0.8374', '-0.2952', '0.1573', '-0.147', '0.213', '-0.5264', '0.0863', '-0.2198', '-0.01332', '0.6626', '-0.4028', '-0.04663', '-0.1519', '-0.39', '-0.2244', '0.383', '-0.1982', '0.5444', '-0.3054', '0.0765', '0.05994']",,0008989,C564479,,,,
mondo:0010369,"nystagmus 5, congenital, X-linked","['nystagmus 5, congenital, X-linked, X-linked dominant', 'NYSTAGMUS 5, congenital, X-linked', 'NYS5']",0111796,300589,,C1845116,,,,,,,,
mondo:0010370,Cornelia de Lange syndrome 2,"['Cornelia De Lange syndrome, X-linked', 'Cornelia DE Lange syndrome 2', 'Cornelia de Lange syndrome 2, X-linked dominant', 'Cornelia de Lange syndrome 2', 'CDLS2', 'Cdls, X-linked', 'Cornelia de Lange syndrome caused by mutation in SMC1A', 'SMC1A Cornelia de Lange syndrome', 'X-linked Cornelia De Lange syndrome', 'Cornelia De Lange syndrome type 2']",0080506,300590,,C1802395,,C75485,,,,,,
mondo:0010371,Aland island eye disease,"['FORSIUS-Eriksson type ocular albinism', 'Aland island eye disease', 'ALAND ISLAND eye disease', 'Forsius Eriksson type ocular albinism', 'Forsius-Eriksson type ocular albinism', 'Åland Islands eye disease', 'Forsius-Eriksson syndrome', 'AIED']",0050630,300600,178333,C0268505,"['-1.269', '0.251', '-0.4148', '-0.3975', '0.3125', '-0.5996', '-0.2343', '0.0924', '-0.04044', '-0.4927', '0.2563', '-0.3289', '-0.3298', '0.3198', '0.0594', '0.2622', '0.10846', '-0.3325', '-0.3037', '-0.7617', '-0.5405', '-0.08264', '0.2888', '0.0762', '-0.422', '-0.1665', '-0.3196', '0.09845', '0.468', '0.7627', '0.4944', '0.01875', '0.2266', '0.1002', '0.1567', '0.0912', '0.03537', '-0.3599', '0.1553', '-0.512', '0.4204', '-0.3489', '-0.2236', '-0.5557', '-0.602', '-0.015', '0.3032', '-0.2344', '0.1841', '0.1632', '0.3967', '0.01628', '-0.387', '-0.464', '0.3357', '-0.634', '1.305', '-0.1384', '-0.4175', '0.09033', '0.3372', '-0.5645', '-0.0665', '0.594', '-0.0968', '-0.356', '0.5054', '0.3215', '-0.08734', '0.567', '-0.2113', '-0.2566', '-0.4163', '0.2465', '0.5405', '0.2007', '-0.03513', '-0.621', '-0.2001', '0.2473', '0.804', '-0.5493', '0.2832', '1.181', '-0.1692', '-0.3691', '0.1482', '-0.1339', '0.58', '0.1667', '0.1415', '0.517', '0.0427', '0.626', '0.978', '-0.1843', '0.11145', '-0.2053', '0.2382', '0.0838']",,,C562664,,H35.5,,
mondo:0010373,premature ovarian failure 2B,"['primary ovarian failure caused by mutation in POF1B', 'premature ovarian failure type 2B', 'premature ovarian failure 2B', 'premature ovarian failure 2B, X-linked recessive', 'POF2B', 'POF1B primary ovarian failure']",0080859,300604,,C1845105,,,,C564476,,,,
mondo:0010374,retinitis pigmentosa 34,"['RP 34', 'retinitis pigmentosa type 34', 'retinitis pigmentosa 34', 'RP34']",0110417,300605,,C1845104,,,,C564475,,H35.5,,
mondo:0010375,"developmental and epileptic encephalopathy, 8","['hyperekplexia and epilepsy', 'epileptic encephalopathy, early infantile, 8', 'early infantile epileptic encephalopathy 8', 'EIEE8', 'epileptic encephalopathy, early infantile, type 8', 'hyperekplexia-epilepsy syndrome', 'developmental and epileptic encephalopathy 8', 'DEE8']",0080215,300607,163985,C1845102,"['0.9517', '0.1722', '-0.3047', '-0.0609', '-0.2715', '-0.4973', '0.81', '0.4407', '-0.6763', '-0.459', '0.07355', '-0.1423', '-0.3694', '0.3848', '-0.1627', '-0.03424', '-0.2927', '-0.4353', '-0.507', '-0.6353', '-0.1968', '0.7393', '-0.0849', '-0.496', '-0.2996', '0.0194', '-0.01675', '-0.1746', '-0.5586', '0.4233', '0.357', '-0.5576', '0.4756', '0.1714', '0.9126', '0.3699', '-0.1277', '-0.1375', '0.01072', '-0.4048', '-0.1614', '-0.418', '-0.05902', '-0.2979', '-0.548', '-0.71', '-0.3499', '0.1991', '0.397', '0.693', '-0.248', '0.1444', '-0.0439', '-0.652', '0.007866', '-0.273', '-0.3545', '-0.0557', '-0.2495', '0.3472', '-0.7725', '0.496', '0.6934', '-0.2416', '-0.5044', '1.492', '0.2229', '0.1849', '-0.9556', '0.7974', '0.9766', '1.024', '-0.1442', '-0.4695', '0.1552', '0.803', '1.031', '0.573', '-0.4668', '0.3843', '-0.1704', '0.8003', '0.513', '0.2861', '0.536', '0.2703', '0.1556', '0.7285', '0.7925', '0.4985', '-0.005787', '0.1707', '-0.43', '0.2942', '0.04138', '0.1799', '0.3206', '-0.56', '0.3425', '0.2559']",,,C564474,,,,
mondo:0010377,"myopia 13, X-linked","['myopia 13', 'myopia 13, X-linked', 'MYP13']",,300613,,C1845096,,,,C564473,,,,
mondo:0010378,X-linked hereditary sensory and autonomic neuropathy with hearing loss,"['DFNX5', 'X-linked hereditary sensory and autonomic neuropathy with deafness', 'deafness, X-linked 5, X-linked recessive', 'deafness, X-linked 5', 'auditory neuropathy, X-linked, 1, with peripheral sensory neuropathy', 'X-linked HSAN with deafness', 'X-linked auditory neuropathy with peripheral sensory neuropathy type 1']",0111741,300614,139583,C4304400,"['0.551', '-0.0959', '-0.553', '0.426', '-0.2542', '-0.6567', '-0.0573', '0.545', '-0.4392', '0.09595', '-0.04272', '0.4465', '0.243', '0.505', '-0.4172', '-0.01403', '-0.2507', '0.924', '-0.88', '-0.727', '0.351', '0.10815', '-0.995', '0.377', '0.266', '-0.0651', '-0.82', '0.01062', '-0.3335', '-0.574', '0.799', '0.02884', '0.2196', '-0.2603', '-0.179', '-0.4548', '0.09467', '0.012535', '-0.0699', '-0.1547', '-0.5034', '-0.1488', '0.007523', '-0.262', '0.2852', '-0.2031', '0.3389', '-0.4048', '-0.10474', '0.05627', '-0.199', '1.343', '0.3433', '-1.36', '0.2598', '0.542', '0.614', '0.2355', '-0.3677', '-0.2207', '0.2394', '0.8086', '0.254', '0.3997', '-0.254', '0.591', '0.4028', '0.605', '-0.1359', '0.4307', '-0.914', '0.04028', '-0.3125', '-0.287', '0.682', '0.4792', '0.1565', '0.914', '-0.4368', '0.759', '0.03903', '-0.5737', '0.2094', '0.519', '0.10455', '-0.2042', '0.532', '0.316', '0.5654', '-0.4998', '0.355', '0.4285', '0.789', '0.05798', '0.992', '0.592', '-0.32', '-0.0689', '0.4211', '0.2067']",,,C564472,,,,
mondo:0010379,Brunner syndrome,"['Brunner syndrome, X-linked recessive', 'monoamine oxidase A deficiency', 'antisocial behavior, X-linked recessive', 'BRNRS', 'Brunner syndrome', 'antisocial behavior, susceptibility to']",0060693,300615,3057,C0796275,"['-0.3872', '0.374', '0.04736', '-0.2344', '-0.12036', '-0.231', '0.08875', '0.0775', '-0.1339', '-0.074', '0.0993', '-0.0977', '0.1792', '-0.10095', '0.0739', '0.01029', '-0.07935', '-0.052', '-0.2544', '-0.5835', '-0.26', '-0.03735', '0.1747', '-0.1913', '-0.0313', '-0.04153', '0.086', '-0.4348', '0.02328', '-0.3198', '-0.03607', '0.02086', '0.3386', '0.594', '-0.3167', '-0.0868', '-0.1193', '-0.287', '-0.2369', '-0.2583', '0.327', '-0.591', '0.01793', '-0.01073', '-0.1509', '-0.4783', '-0.004658', '-0.0447', '0.0046', '0.4155', '-0.04565', '0.2869', '-0.2717', '-0.05603', '0.357', '-0.09174', '0.217', '-0.298', '-0.1406', '0.1572', '-0.05392', '0.0659', '0.1549', '-0.1293', '-0.10156', '0.1729', '0.2844', '0.293', '-0.262', '0.10315', '-0.3904', '0.00809', '-0.034', '0.002832', '0.2198', '0.401', '-0.00879', '-0.1951', '-0.1277', '-0.02144', '0.131', '-0.1694', '-0.05502', '0.5', '0.4875', '0.423', '-0.1404', '0.1182', '0.4143', '0.3047', '0.313', '0.4373', '-0.1935', '-0.03763', '0.4392', '0.269', '0.273', '-0.386', '0.4128', '0.444']",,,C563156,,,,
mondo:0010380,"cataract, ataxia, short stature, and intellectual disability","['cataract, ataxia, short stature, and mental retardation', 'cataract, ataxia, short stature, and intellectual disability', 'cataracts, ataxia, short stature, and intellectual disability', 'cataracts, ataxia, short stature, and mental retardation', 'Casm syndrome']",,300619,,C1845094,,,,C535345,,,,
mondo:0010381,Tn polyagglutination syndrome,"['Tn polyagglutination syndrome, somatic', 'galactosyltransferase deficiency', 'Tn polyagglutination syndrome', 'TNPS']",0080520,300622,,C0272137,,,,C562719,,,,
mondo:0010382,fragile X-associated tremor/ataxia syndrome,"['FXTAS syndrome', 'fragile 10 tremor/ataxia syndrome', 'FXTAS', 'Fragile X tremor/ataxia syndrome, X-linked dominant', 'fragile X tremor/ataxia syndrome']",0050879,300623,93256,C1839780,"['-0.02847', '-0.04922', '-0.12146', '-0.02988', '-0.06793', '-0.665', '0.3528', '0.305', '-0.6104', '-0.8013', '0.04013', '0.2114', '-0.0887', '0.2123', '0.5864', '-0.2206', '-0.2101', '-0.1045', '0.1826', '-0.81', '-0.1539', '-0.5386', '0.001379', '-0.4846', '0.2615', '-0.569', '-0.0747', '-0.1624', '0.1016', '-0.657', '0.1065', '0.2944', '-0.313', '-0.3545', '0.346', '0.1431', '-0.1501', '0.04514', '0.4402', '0.358', '0.3823', '0.04227', '-0.3093', '0.3914', '0.5376', '-0.7705', '0.0592', '0.3894', '0.3762', '-0.1323', '-0.1168', '0.2092', '0.03784', '-0.3823', '-0.04654', '-0.715', '0.4153', '0.55', '-0.2014', '0.2493', '-0.4924', '0.3953', '0.328', '-0.1835', '-0.2595', '0.436', '0.1489', '0.4685', '-0.547', '0.3867', '0.5977', '0.3816', '-0.1501', '-0.512', '0.504', '0.1713', '0.4211', '0.3215', '0.1364', '0.3442', '-0.1345', '-1.038', '0.3606', '0.64', '-0.00941', '-0.4202', '0.1965', '-0.0504', '0.4976', '0.4446', '0.2866', '0.454', '0.0921', '-0.09045', '0.688', '0.68', '0.2983', '0.37', '-0.04437', '0.1191']",C126566,,C564105,,,,
mondo:0010383,fragile X syndrome,"['Fragile X syndrome, X-linked dominant', 'FraX syndrome', 'fragile 10 premature ovarian failure', 'intellectual disability, X-linked, associated with Marxq28', 'primary ovarian insufficiency, fragile X-associated', 'fragile X mental retardation syndrome', 'marker 10 syndrome', 'fragile 10 syndrome', 'mental retardation, X-linked, associated with Marxq28', 'fragile X intellectual disability syndrome', 'Martin-Bell syndrome', 'fragile 10 intellectual disability syndrome', 'FRAXA syndrome', 'marker X syndrome', 'X-linked mental retardation and macroorchidism', 'FXS', 'fragile X syndrome', 'fragile 10 mental retardation syndrome', 'fra(X) syndrome', 'X-linked intellectual disability and macroorchidism']",14261,300624,908,C0016667,"['0.3987', '0.3835', '0.4114', '-0.5093', '0.2357', '-0.1765', '0.3057', '0.741', '-1.084', '-0.26', '-0.0869', '-0.04904', '0.4966', '0.3438', '-0.1346', '0.2014', '0.02875', '-0.2261', '0.1788', '-0.281', '-0.1466', '-0.2444', '0.04852', '-0.1864', '0.3276', '-0.4043', '0.204', '-0.235', '0.4119', '-0.3213', '0.7817', '0.2113', '0.6143', '0.10876', '-0.0708', '-0.3306', '-0.3652', '-0.4392', '-0.181', '-0.4587', '0.4956', '-0.272', '-0.4004', '0.03001', '0.864', '-0.344', '-0.3345', '-0.007698', '0.1729', '0.57', '-0.64', '0.5947', '-0.794', '-0.04797', '0.1398', '0.2861', '0.4187', '-0.3577', '0.0981', '0.2983', '-0.04834', '0.4692', '-0.0865', '0.534', '0.0706', '0.5737', '-0.6284', '-0.1459', '-0.1682', '0.2084', '-0.1345', '-0.4312', '-0.732', '-0.2656', '0.2131', '0.3303', '0.2546', '0.393', '-0.02914', '-0.502', '0.3118', '-0.318', '-0.0437', '0.2742', '0.2396', '0.3835', '-0.682', '0.2133', '-0.0606', '0.606', '-0.3936', '0.435', '-0.3145', '0.0327', '0.747', '-0.0177', '0.0892', '-0.4556', '0.3367', '0.0975']",C84717,,D005600,759.83,,10017324,
mondo:0010384,"hypospadias 1, X-linked","['HYSP1', 'hypospadias 1, X-linked, X-linked recessive', 'hypospadias 1, X-linked']",,300633,,C2678098,,,,C567482,,,,
mondo:0010385,X-linked lymphoproliferative disease due to XIAP deficiency,"['X-linked lymphoproliferative syndrome type 2', 'Xiap deficiency', 'XIAP deficiency/XLPs', 'lymphoproliferative syndrome, X-linked, 2', 'XIAP deficiency', 'XIAP-related lymphoproliferative disease, X-linked', 'lymphoproliferative syndrome, X-linked, type 2', 'lymphoproliferative syndrome, X-linked, 2, X-linked recessive', 'XLP2']",0060706,300635,538934,C1845076,,C126295,,C564469,,,,
mondo:0010386,immunodeficiency 33,"['atypical Mycobacteriosis, familial, X-linked 1', 'invasive pneumococcal disease, recurrent isolated, type 2', 'NF-kappa B essential modulator deficiency', 'immunodeficiency 33, Mycobacteriosis, X-linked', 'invasive pneumococcal disease, recurrent isolated, 2', 'immunodeficiency 33, X-linked recessive', 'immunodeficiency, Pure', 'immunodeficiency type 33', 'invasive pneumococcal disease, recurrent isolated caused by mutation in IKBKG', 'immunodeficiency without anhidrotic ectodermal dysplasia', 'IMD33', 'familial X-linked 1 atypical mycobacteriosis', 'immunodeficiency, isolated', 'IKBKG invasive pneumococcal disease, recurrent isolated', 'NEMO deficiency syndrome', 'IPD2']",0112003,300636,,C1970879,,,,C567070,,,,
mondo:0010388,"rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked","['RESDX', 'ROLANDIC epilepsy, intellectual disability, and speech dyspraxia, X-linked', 'rolandic epilepsy, impaired intellectual development, and speech dyspraxia', 'rolandic epilepsy, mental retardation, and speech dyspraxia, X-linked', 'rolandic epilepsy, intellectual disability, and speech dyspraxia, X-linked', 'ROLANDIC epilepsy, mental retardation, and speech dyspraxia, X-linked']",,300643,,C1845070,,,,C564467,,,,
mondo:0010389,X-linked Mendelian susceptibility to mycobacterial diseases due to CYBB deficiency,"['CYBB X-linked mendelian susceptibility to mycobacterial diseases', 'X-linked MSMD due to CYBB deficiency', 'IMD34', 'immunodeficiency type 34', 'immunodeficiency 34, Mycobacteriosis, X-linked', 'immunodeficiency 34', 'immunodeficiency 34, mycobacteriosis, X-linked, X-linked recessive', 'atypical Mycobacteriosis, familial, X-linked 2']",0112000,300645,319623,C1970859,"['-0.2139', '0.221', '0.0391', '-0.09644', '0.2156', '-0.3118', '0.05975', '-0.0716', '-0.1278', '-0.309', '0.09924', '0.0898', '-0.2103', '0.04025', '0.3281', '-0.1692', '-0.07635', '0.06976', '-0.1877', '-0.3188', '0.1271', '-0.10516', '0.1716', '0.00435', '-0.2432', '-0.02156', '-0.1833', '0.0254', '-0.1475', '-0.2203', '0.07513', '0.04608', '0.3635', '0.1155', '0.2307', '-0.3643', '-0.02347', '-0.2194', '-0.11273', '-0.3157', '0.016', '-0.1455', '0.1565', '-0.1228', '-0.2379', '-0.4756', '0.1367', '0.005962', '0.1261', '0.1259', '-0.0594', '-0.1948', '0.2502', '-0.03436', '-0.05386', '-0.09424', '0.4688', '0.03525', '-0.1392', '0.1593', '0.03998', '0.2856', '0.157', '0.169', '0.2974', '0.2427', '0.1447', '0.1499', '-0.2666', '0.228', '-0.1643', '-0.1279', '-0.01397', '-0.1876', '0.2101', '0.1538', '0.1284', '0.0815', '-0.0614', '0.1317', '-0.2233', '0.1105', '0.05048', '0.2832', '-0.0765', '-0.1465', '0.41', '0.304', '0.3098', '-0.02051', '0.25', '0.0996', '-0.1573', '-0.22', '0.594', '0.4695', '0.2612', '-0.3252', '-0.02356', '-0.0824']",,,C567068,,,,
mondo:0010390,ocular albinism with late-onset sensorineural deafness,"['albinism, ocular, with late-onset sensorineural deafness', 'ocular albinism with sensorineural deafness', 'OASD', 'deafness and ocular albinism', 'albinism ocular late onset sensorineural deafness']",,300650,1000,C1845069,,,,,,,,
mondo:0010391,"angioma serpiginosum, X-linked","['angioma serpiginosum, X-linked', 'angio serpiginosum, X-linked dominant']",,300652,,,,,,C536366,,,,
mondo:0010392,glycogen storage disease due to phosphoglycerate kinase 1 deficiency,"['PGK deficiency', 'phosphoglycerate kinase 1 deficiency, X-linked recessive', 'Phosphoglycerate kinase deficiency', 'GSD due to phosphoglycerate kinase 1 deficiency', 'PGK1 glycogen storage disease', 'glycogen storage disease caused by mutation in PGK1', 'PHOSPHOGLYCERATE KINASE 1 deficiency', 'Pgk1 deficiency', 'glycogenosis due to phosphoglycerate kinase 1 deficiency']",0111933,300653,713,C1970848,"['-0.6685', '-0.1288', '-0.7505', '-0.1267', '-0.1606', '-0.2527', '-0.1028', '0.707', '-0.1696', '-0.337', '0.00434', '-0.0694', '-0.1061', '-0.0941', '-0.3848', '0.08203', '-0.04114', '-0.3381', '-1.089', '-0.6636', '0.7227', '0.10944', '0.253', '0.0801', '-0.5', '-0.788', '0.1411', '-0.482', '0.0363', '-0.344', '0.4265', '-0.4648', '0.4602', '0.4702', '-0.25', '-0.511', '-0.848', '-0.5454', '-0.295', '0.2222', '0.03714', '-0.4524', '0.6665', '-0.146', '-0.1931', '-0.2666', '0.1691', '-0.4756', '-0.3696', '0.05664', '-0.01848', '0.2429', '0.1255', '0.2139', '0.3037', '-0.2439', '0.9126', '-0.2487', '-0.3813', '0.004177', '0.308', '-0.3123', '0.568', '0.000865', '-0.8486', '-0.235', '0.2542', '0.696', '-0.3645', '0.04007', '-0.1744', '-0.266', '-0.138', '0.5776', '0.1957', '0.6304', '0.4902', '-0.1499', '-0.01576', '0.02843', '0.3699', '-0.2286', '0.3796', '0.7056', '0.2817', '0.2184', '0.1335', '0.491', '0.12494', '-0.1235', '0.7217', '0.062', '0.2751', '-0.71', '0.829', '1.141', '0.00757', '-0.4478', '0.284', '-0.0701']",C126738,,C567067,,,,
mondo:0010393,"intellectual disability, X-linked 93","['intellectual disability, X-linked type 93', 'BRWD3 non-syndromic X-linked intellectual disability', 'mental retardation, X-linked 93', 'intellectual developmental disorder, X-linked 93, X-linked recessive', 'mental retardation, X-linked type 93', 'intellectual disability, X-linked, with macrocephaly', 'intellectual disability, X-linked 93', 'MRX93', 'non-syndromic X-linked intellectual disability caused by mutation in BRWD3', 'mental retardation, X-linked, with macrocephaly']",0112045,300659,,C1970841,,,,C567066,,,,
mondo:0010395,phosphoribosylpyrophosphate synthetase superactivity,"['PRPS1 superactivity', 'phosphoribosylpyrophosphate synthetase superactivity, X-linked recessive', 'PRPP synthetase superactivity', 'phosphoribosylpyrophosphate synthetase superactivity', 'gout, PRPS-related', 'gout, PRPS-related, X-linked recessive']",0111260,300661,3222,C1970827,"['-0.2224', '-0.03726', '-0.2944', '-0.2776', '0.1393', '-0.602', '-0.3154', '0.715', '-0.6514', '0.4976', '0.02246', '-0.6', '0.2417', '0.0552', '0.03995', '-0.2', '-0.4915', '0.1885', '-0.4658', '-0.651', '0.3357', '-0.03043', '0.4304', '-0.1987', '-0.0359', '-0.296', '0.2019', '-0.4763', '0.3025', '0.3623', '-0.0754', '-0.06247', '-0.0388', '0.4575', '-0.2225', '-0.904', '-0.1868', '-0.05194', '-0.1646', '-0.2462', '0.777', '-0.898', '0.7476', '-0.416', '-0.7285', '-0.421', '-0.4197', '-0.5566', '0.0952', '0.5435', '-0.3494', '0.1037', '0.5566', '-0.4824', '0.0775', '-0.6333', '0.6357', '-0.376', '-0.07245', '0.01487', '-0.10364', '0.4463', '-0.2788', '0.2439', '0.3987', '-0.1941', '0.4202', '0.06683', '-0.1581', '-0.5327', '-0.379', '-0.006824', '0.01305', '0.1942', '0.4956', '0.08307', '-0.06635', '0.3496', '-0.4272', '0.569', '-0.1852', '0.1189', '0.05072', '0.667', '0.529', '1.064', '-0.361', '-0.1087', '0.2585', '0.668', '0.2927', '1.077', '-0.7383', '-0.4639', '0.4812', '0.5264', '0.3481', '-0.516', '0.06525', '-0.0769']",,,C567064,,,,
mondo:0010396,"developmental and epileptic encephalopathy, 2","['epileptic encephalopathy, early infantile, type 2', 'infantile spasm syndrome, X-linked 2', 'EIEE2', 'epileptic encephalopathy, early infantile, 2', 'CDKL5 early infantile epileptic encephalopathy', 'developmental and epileptic encephalopathy 2, X-linked dominant', 'early infantile epileptic encephalopathy caused by mutation in CDKL5', 'DEE2']",0080467,300672,505652,C1839333,,,,C564064,,,,
mondo:0010397,severe neonatal-onset encephalopathy with microcephaly,"['severe congenital encephalopathy due to MECP2 mutation', 'encephalopathy, neonatal severe, X-linked recessive', 'severe neonatal encephalopathy due to MECP2 mutations', 'encephalopathy, neonatal severe, due to MECP2 mutations']",0111932,300673,209370,C1968556,"['-0.1497', '0.3784', '0.4685', '-0.1327', '0.2585', '-0.06854', '0.5513', '0.801', '-1.018', '-0.1432', '0.06696', '0.1195', '0.4', '0.4963', '0.498', '-0.0852', '0.7515', '0.2174', '-0.3557', '-1.032', '-0.07104', '-0.1168', '0.312', '-0.0548', '0.1471', '0.0485', '0.1008', '0.2073', '0.1146', '-0.1544', '-0.2954', '-0.2778', '0.463', '-0.05252', '-0.4421', '0.808', '-0.4075', '-0.445', '-0.02869', '-0.1478', '0.3896', '0.209', '-0.5425', '-0.3445', '0.1455', '-0.504', '0.5933', '-0.1359', '0.01012', '0.2954', '0.08826', '-0.514', '-0.1562', '-0.3298', '0.0722', '0.2413', '-0.65', '0.6094', '-0.4346', '0.2737', '0.2476', '0.5674', '0.5107', '-0.02538', '-0.1267', '-0.2751', '0.597', '-0.0631', '-1.267', '0.000986', '-0.475', '1.136', '0.4517', '-0.6274', '-0.1642', '0.2416', '0.7056', '-0.1531', '-0.3906', '0.03525', '-0.407', '1.095', '-0.2252', '0.2156', '0.1927', '-0.2466', '0.588', '-0.1624', '0.843', '0.3567', '-0.01405', '0.101', '-0.1362', '0.2258', '-0.3384', '0.5483', '0.9116', '-0.5483', '0.875', '-0.5693']",C132293,,C566878,,,,
mondo:0010398,syndromic X-linked intellectual disability 14,"['intellectual disability, X-linked, syndromic type 14', 'intellectual developmental disorder, X-linked syndromic 14, X-linked recessive', 'mental retardation, X-linked, syndromic 14', 'UPF3B X-linked syndromic intellectual disability', 'X-linked syndromic intellectual disability caused by mutation in UPF3B', 'syndromic X-linked intellectual disability type 14', 'mental retardation, X-linked, syndromic type 14', 'MRXS14', 'intellectual disability, X-linked, syndromic 14']",0060821,300676,323,C1970822,,,,C567063,,,,
mondo:0010399,chromosome Xp21 deletion syndrome,"['Glycerol kinase deficiency-contiguous gene syndrome', 'Xp21 microdeletion syndrome', 'Complex Glycerol kinase deficiency', 'monosomy Xp21', 'Xp21 contiguous gene deletion syndrome', 'chromosome Xp21 deletion syndrome', 'complex glycerol kinase deficiency', 'Del(X)(p21)']",0060427,300679,261476,C0795887,,,,,277.6,,,
mondo:0010400,X-linked scapuloperoneal muscular dystrophy,"['SPM', 'scapuloperoneal myopathy, X-linked dominant', 'X-linked scapuloperoneal syndrome', 'X-linked SPMD', 'scapuloperoneal myopathy, X-linked dominant, X-linked dominant', 'scapuloperoneal myopathy, FHL1-related']",,300695,431272,C2678061,,,,,,,,
mondo:0010401,X-linked myopathy with postural muscle atrophy,"['Ehlers-Danlos syndrome, classic-like, 1', 'Emery-Dreifuss muscular dystrophy 6, X-linked', 'myopathy, X-linked, with postural muscle atrophy', 'XMPMA', 'myopathy, X-linked, with postural muscle atrophy, X-linked recessive']",0070251,300696,178461,C2678055,"['-0.8447', '0.4297', '-0.1951', '-0.3105', '0.0431', '-0.8403', '0.3396', '0.666', '-1.286', '-0.3242', '-0.1997', '0.1294', '-0.1527', '-0.02194', '0.3867', '0.1895', '-0.1337', '-0.338', '-0.4045', '-0.711', '0.1598', '0.1661', '0.459', '0.5166', '0.1659', '-0.006317', '0.3806', '-0.4844', '-0.3481', '-0.0897', '0.3447', '0.53', '0.2883', '-0.08325', '0.09393', '-0.1605', '0.0596', '-0.2188', '0.2003', '-0.4365', '-0.2556', '-0.5127', '-0.1677', '0.4443', '-0.2354', '0.03522', '-0.44', '0.2291', '-0.1738', '0.3418', '-0.10785', '0.2502', '0.3513', '-0.05423', '-0.06335', '-0.811', '0.7554', '-0.06122', '0.0736', '0.02042', '0.3108', '0.05618', '-0.17', '0.2206', '-0.3943', '-0.00822', '0.525', '0.5933', '-0.013985', '-0.0468', '-0.293', '-0.2546', '0.295', '0.12463', '0.4424', '0.2211', '0.07526', '0.01828', '-0.03656', '-0.1609', '0.2048', '-0.0733', '0.2101', '0.364', '-0.1774', '0.3147', '0.042', '0.295', '0.379', '-0.2124', '0.265', '-0.07367', '0.516', '0.2266', '0.49', '0.343', '0.7554', '-0.08746', '0.0733', '0.0711']",,,,,,,
mondo:0010402,syndromic X-linked intellectual disability 94,"['MRX94', 'intellectual disability, X-linked, syndromic, Wu type', 'syndromic X-linked mental retardation Wu type', 'MRXS29', 'syndromic X-linked mental retardation 29', 'syndromic X-linked intellectual disability type 94', 'intellectual disability, X-linked, syndromic 29', 'mental retardation, X-linked, syndromic, Wu type', 'intellectual disability, X-linked 94', 'syndromic X-linked intellectual disability 29', 'syndromic X-linked intellectual disability due to GRIA3 anomalies', 'intellectual developmental disorder, X-linked, syndromic, Wu type, X-linked recessive', 'mental retardation, X-linked, syndromic 29', 'mental retardation, X-linked 94', 'MRXSW', 'syndromic X-linked intellectual disability Wu type']",0060823,300699,,C2678051,,,,C567479,,,,
mondo:0010403,albinism-hearing loss syndrome,"['Woolf^s syndrome', 'Woolf syndrome', 'Ziprkowski–Margolis syndrome', 'albinism deafness syndrome', 'ADFN', 'ALDS', 'albinism-deafness syndrome']",,300700,998,,,,,C537042,,,,
mondo:0010404,X-linked non progressive cerebellar ataxia,"['X-linked spinocerebellar ataxia type 5', 'SCAX5', 'spinocerebellar ataxia, X-linked 5', 'spinocerebellar ataxia, X-linked 5, X-linked recessive']",0111833,300703,314978,C2678048,,,,C567478,,,,
mondo:0010405,"prostate cancer, hereditary, X-linked 2","['HPCX2', 'prostate cancer, hereditary, X-linked 2']",,300704,,C2678047,,,,C567477,,,,
mondo:0010406,chromosome Xp11.22 duplication syndrome,"['mental retardation, X-linked 31', 'intellectual disability, X-linked 17', 'chromosome Xp11.22 duplication syndrome', 'Xp11.22-linked intellectual disability', 'mental retardation, X-linked 17', 'intellectual disability, X-linked 31', 'Xp11.22 microduplication syndrome']",0112037,300705,,,,,,,,,,
mondo:0010407,"intellectual disability, X-linked syndromic, Turner type","['mental retardation, X-Linked, with growth retardation, deafness, and microgenitalism', 'Brooks Wisniewski Brown syndrome', 'mental retardation, X-linked, syndromic, Turner type', 'X-linked mental retardation Brooks type', 'Juberg-Marsidi Syndrome', 'mental retardation, X-linked, syndromic, Brooks-Wisniewski-Brown type', 'mental retardation, X-linked, syndromic, Brooks-Wisniewski-Brown Type', 'syndromic X-linked intellectual disability Turner type', 'X-linked intellectual disability, Brooks type', 'Brooks-Wisniewski-Brown Syndrome', 'MRXST', 'mental retardation and macrocephaly syndrome', 'Brooks-Wisniewski-Brown syndrome', 'X-linked intellectual disability, Turner type']",0060829,309590,85328,C2678046,,,,C567476,,,,
mondo:0010408,syndactyly-telecanthus-anogenital and renal malformations syndrome,"['syndactyly, telecanthus, anogenital and renal malformations', 'toe syndactyly, telecanthus, anogenital and renal malformations', 'STAR', 'syndactyly with renal and anogenital malformations', 'Star syndrome', 'STAR syndrome, X-linked dominant', 'toe syndactyly, telecanthus, and anogenital and renal malformations', 'STAR syndrome']",0111931,300707,140952,C2678045,"['0.07654', '0.08154', '0.3372', '-0.06506', '0.1203', '-0.328', '0.05276', '0.6914', '-0.5093', '-0.3953', '-0.10223', '-0.05197', '-0.0711', '-0.2598', '-0.149', '0.1393', '0.52', '-0.3044', '-0.477', '-0.2211', '0.1758', '0.0746', '0.1523', '-0.1954', '0.1907', '0.063', '-0.2542', '0.4934', '0.7476', '-0.2207', '0.2053', '-0.485', '0.4683', '-0.181', '0.368', '-0.3574', '0.29', '-0.3665', '0.2306', '-0.08307', '0.05774', '-0.2355', '0.05078', '-0.402', '-0.01275', '-0.259', '0.2517', '0.2239', '-0.3938', '-0.4377', '-0.558', '-0.1302', '-0.1642', '0.2473', '-0.3735', '-0.1729', '0.337', '0.157', '-0.3591', '0.0452', '0.279', '0.4116', '-0.3054', '-0.1003', '0.2338', '-0.11847', '-0.07556', '0.3743', '-0.6455', '0.09357', '-0.4397', '0.2256', '0.1807', '0.2355', '0.03683', '0.1415', '0.281', '-0.03064', '-0.5044', '-0.02415', '0.1035', '0.1103', '0.2203', '0.512', '0.03111', '-0.04623', '-0.0734', '0.5674', '-0.1494', '0.03842', '-0.0943', '0.2888', '0.3186', '-0.0672', '0.926', '0.005573', '0.4858', '-1.016', '0.3206', '0.1819']",,,C567475,,,,
mondo:0010409,syndromic X-linked intellectual disability Shrimpton type,"['MRXS9', 'intellectual disability, X-linked, syndromic 9', 'mental retardation, X-linked, syndromic 9', 'X-linked intellectual disability, Shrimpton type']",0060813,300709,85324,C2678039,,,,C567474,,,,
mondo:0010410,"alopecia, androgenetic, 2","['alopecia, androgenetic, 2', 'AGA2']",,300710,,C2678038,,,,C567473,,,,
mondo:0010411,"pyloric stenosis, infantile hypertrophic, 4","['IHPS4', 'pyloric stenosis, infantile hypertrophic, 4']",,300711,,C2678037,,,,C567472,,,,
mondo:0010412,X-linked intellectual disability-craniofacioskeletal syndrome,"['craniofacioskeletal syndrome, X-linked recessive, X-linked dominant', 'craniofacioskeletal syndrome']",,300712,163979,C2678036,,,,C567471,,,,
mondo:0010413,"intellectual disability, X-linked 95","['MRX95', 'mental retardation, X-linked 95', 'intellectual disability, X-linked 95', 'mental retardation, X-linked 95, X-linked dominant']",,300716,,C2678034,,,,C567470,,,,
mondo:0010414,"myopathy, reducing body, X-linked, early-onset, severe","['myopathy, reducing body, X-linked, early-onset, severe', 'reducing body myopathy, X-linked 1a, severe, infantile or early childhood onset, X-linked dominant', 'RBMX1A', 'reducing body myopathy, X-linked 1A, severe, with infantile or early childhood onset']",,300717,,C2678027,,,,C567469,,,,
mondo:0010415,"myopathy, reducing body, X-linked, childhood-onset","['reducing body myopathy, X-linked 1B, with late childhood or adult onset', 'myopathy, reducing body, X-linked, childhood-onset', 'RBMX1B']",0080687,300718,,C2678015,,,,C567468,,,,
mondo:0010416,"deafness, cataract, retinitis pigmentosa, and sperm abnormalities","['deafness, cataract, retinitis pigmentosa, and sperm abnormalities', 'deafness, cataract, retinitis pigmentosa, and sperm abnormalities, X-linked recessive']",,300719,,C2678011,,,,C567467,,,,
mondo:0010417,syndromic X-linked intellectual disability Najm type,"['mental retardation and microcephaly with pontine and cerebellar hypoplasia', 'Micpch syndrome', 'intellectual developmental disorder and microcephaly with pontine and cerebellar hypoplasia, X-linked dominant', 'X-linked intellectual disability, Najm type', 'mental retardation, X-linked, syndromic, Najm type', 'intellectual disability and microcephaly with pontine and cerebellar hypoplasia', 'intellectual disability, X-linked, syndromic, Najm type', 'X-linked intellectual disability-microcephaly-pontocerebellar hypoplasia syndrome', 'mental retardation and microcephaly with PONTINE and cerebellar hypoplasia', 'microcephaly with pontine and cerebellar hypoplasia', 'intellectual disability and microcephaly with PONTINE and cerebellar hypoplasia', 'MICPCH', 'X-linked intellectual disability - microcephaly - pontocerebellar hypoplasia']",0060807,300749,163937,C2677903,"['-0.1873', '0.10266', '0.0607', '-0.1208', '0.11896', '-0.2031', '-0.04056', '0.5396', '-0.6094', '-0.4438', '-0.2168', '-0.4917', '-0.28', '-0.1201', '0.07086', '0.03662', '0.7437', '-0.1746', '-0.10583', '-0.4297', '-0.1946', '0.2886', '0.2335', '-0.2964', '0.1375', '-0.02182', '-0.589', '-0.1371', '0.2388', '-0.001828', '0.514', '-0.1459', '0.666', '0.0775', '-0.128', '-0.166', '-0.5635', '-0.5977', '-0.3376', '0.09326', '0.525', '-0.0482', '0.0431', '-0.11444', '-0.0899', '-0.2367', '0.0754', '0.2585', '-0.2435', '-0.2311', '0.1017', '0.04544', '-0.2239', '-0.2261', '0.12274', '-0.003199', '0.347', '-0.2261', '0.06134', '0.2817', '-0.243', '-0.1334', '0.03102', '0.3584', '-0.3508', '-0.0639', '0.04175', '0.593', '-0.648', '0.251', '-0.2632', '0.6', '0.2234', '-0.1678', '0.4285', '-0.0366', '0.4492', '-0.3984', '-0.01904', '-0.00938', '0.1833', '-0.1838', '0.144', '0.8604', '0.08746', '0.4915', '-0.1827', '0.2944', '0.3025', '0.2161', '0.1239', '0.713', '-0.07605', '0.2424', '0.72', '0.3162', '0.2966', '0.05438', '0.5063', '0.303']",,,C567466,,,,
mondo:0010418,hereditary spastic paraplegia 34,"['spastic paraplegia 34, X-linked', 'X-linked spastic paraplegia 34', 'SPG34', 'X-linked spastic paraplegia type 34', 'hereditary spastic paraplegia type 34', 'spastic paraplegia 34, X-linked, X-linked recessive']",0110785,300750,171607,C2677897,,,,C567465,,,,
mondo:0010420,X-linked erythropoietic protoporphyria,"['XLPP', 'Erythrohepatic protoporphyria, X-linked', 'X-linked dominant protoporphyria', 'XLP', 'protoporphyria, erythropoietic, X-linked', 'XLEPP', 'X-linked dominant erythropoietic protoporphyria', 'XLDPP', 'protoporphyria, erythropoietic, X-linked dominant', 'erythropoietic protoporphyria, X-linked']",,300752,79278,,,,,C567464,,,,
mondo:0010421,Bruton-type agammaglobulinemia,"['Bruton agammaglobulinemia tyrosine kinase deficiency', 'BTK-deficiency', 'Bruton^s Sex-linked agammaglobulinemia', 'Bruton^s X-linked agammaglobulinemia', 'XLA', 'agammaglobulinemia, Bruton tyrosine kinase', 'Bruton type agammaglobulinemia', 'agammaglobulinemia, X-linked 1, X-linked recessive', 'Bruton^s agammaglobulinemia', 'agammaglobulinemia, BTK', 'immunodeficiency 1', 'hypogammaglobulinemia, X-linked', 'Bruton^s type agammaglobulinemia', 'Bruton-type agammaglobulinemia', 'agammaglobulinemia, X-linked', 'BTK deficiency', 'X-linked agammaglobulinemia', 'agammaglobulinemia, X-linked, type 1', 'Bruton^s agammaglobulinaemia']",14179,300755,47,C0221026,"['0.2722', '0.002512', '-0.606', '-0.1664', '0.03014', '-0.2903', '0.1677', '0.295', '-0.11224', '-0.06946', '0.2085', '0.57', '-0.2279', '0.6626', '0.01528', '0.010765', '0.1887', '0.504', '-0.6997', '-0.61', '-0.1898', '-0.2517', '0.95', '-0.48', '-0.0923', '0.05212', '-0.7275', '-0.01917', '-0.376', '-0.6187', '0.4915', '0.3376', '0.1227', '0.1953', '-0.2229', '0.4597', '-1.006', '0.2664', '-0.3103', '0.1918', '-0.5156', '-0.335', '0.1392', '-0.261', '0.09424', '-0.1165', '-0.618', '-0.5654', '-0.2195', '0.0404', '0.259', '-0.3174', '0.049', '-0.105', '0.1998', '0.4863', '0.3486', '-0.596', '-0.3167', '0.2532', '0.1476', '0.5903', '-0.0969', '0.4675', '0.748', '-0.3362', '0.857', '0.3477', '0.0407', '0.4866', '-0.0711', '-0.4236', '-0.707', '-0.38', '0.2347', '0.0911', '0.3965', '-0.2063', '-0.1184', '-0.1084', '-0.1523', '-0.01402', '0.3882', '0.4058', '-0.0678', '0.3826', '0.2006', '-0.0831', '-0.1088', '0.1914', '0.12054', '0.6963', '-0.2192', '0.318', '0.7227', '0.4536', '0.05167', '-0.801', '-0.05408', '-0.1615']",C3822,,C537409,,,10060360,
mondo:0010422,Alzheimer disease 16,"['Alzheimer^s disease type 16', 'Alzheimer^s disease 16', 'AD16', 'Alzheimer disease 16']",0110036,300756,,C2677888,,,,C567463,,,,
mondo:0010423,"hypospadias 2, X-linked","['HYSP2', 'hypospadias 2, X-linked, X-linked recessive', 'hypospadias 2, X-linked']",,300758,,C2677879,,,,C567462,,,,
mondo:0010424,"surfactant metabolism dysfunction, pulmonary, 4","['pulmonary alveolar proteinosis, congenital, 4', 'SMDP4', 'Pap due to Csf2Ra deficiency', 'surfactant metabolism dysfunction, pulmonary, type 4', 'Csf2Ra deficiency', 'surfactant metabolism dysfunction, pulmonary, 4']",,300770,,C2677877,,,,C567461,,,,
mondo:0010425,Lisch epithelial corneal dystrophy,"['corneal dystrophy, Lisch epithelial', 'band-Shaped and whorled microcystic corneal epithelial dystrophy', 'Lisch epithelial corneal dystrophy', 'band-shaped and whorled microcystic dystrophy of the corneal epithelium', 'LECD', 'band-shaped and whorled microcystic', 'corneal dystrophy, Lisch epithelial, X-linked dominant']",0060450,300778,98955,C2749050,,,,C567588,,,,
mondo:0010426,X-linked endothelial corneal dystrophy,"['endothelial corneal dystrophy, X-linked', 'corneal dystrophy, endothelial, X-linked', 'XECD', 'corneal dystrophy, endothelial, X-linked, X-linked dominant']",0060446,300779,293621,C2749049,,,,C567587,,,,
mondo:0010427,syndromic X-linked intellectual disability Raymond type,"['mental retardation, X-linked, syndromic, Raymond type', 'intellectual disability, X-linked, syndromic, Raymond type', 'MRXSR', 'mental retardation, X-linked syndromic, Raymond type', 'intellectual disability, X-linked syndromic, Raymond type']",0060824,300799,,C3275406,,,,,,,,
mondo:0010428,chromosome Xp11.23-p11.22 duplication syndrome,"['chromosome xp11.23-p11.22 duplication syndrome, X-linked dominant', 'trisomy Xp11.22-p11.23', 'Xp11.22-p11.23 Microduplication', 'microduplication Xp11.22-p11.23 syndrome', 'chromosome Xp11.23-p11.22 duplication syndrome']",0060461,300801,217377,,,,,C567585,,,,
mondo:0010429,"intellectual disability, X-linked 96","['mental retardation, X-linked type 96', 'intellectual disability, X-linked 96', 'MRX96', 'non-syndromic X-linked intellectual disability caused by mutation in SYP', 'mental retardation, X-linked 96', 'intellectual disability, X-linked type 96', 'SYP non-syndromic X-linked intellectual disability', 'intellectual developmental disorder, X-linked 96, X-linked recessive']",0112035,300802,,C3275408,,,,,,,,
mondo:0010430,"intellectual disability, X-linked 97","['intellectual disability, X-linked type 97', 'mental retardation, X-linked type 97', 'Mrxz', 'intellectual developmental disorder, X-linked 97', 'mental retardation, X-linked 65', 'ZNF711 non-syndromic X-linked intellectual disability', 'intellectual disability, X-linked 97', 'non-syndromic X-linked intellectual disability caused by mutation in ZNF711', 'mental retardation, X-linked 97', 'MRX97', 'intellectual disability, X-linked 65']",0112046,300803,,C2749020,,,,C567583,,,,
mondo:0010431,Joubert syndrome 10,"['Joubert syndrome 10, X-linked recessive', 'OFD1 Joubert syndrome', 'Joubert syndrome type 10', 'JBTS10', 'Joubert syndrome caused by mutation in OFD1', 'Joubert syndrome 10']",0110981,300804,,C2749019,,,,C567582,,,,
mondo:0010432,"thrombophilia, X-linked, due to factor 9 defect","['thrombophilia, X-linked, due to factor IX defect', 'deep Venous thrombosis, protection against', 'THPH8', 'deep venous thrombosis, protection against, X-linked recessive', 'thrombophilia 8, X-linked, due to factor IX defect, X-linked recessive']",0111899,300807,,C2749016,"['-0.0891', '0.1138', '-0.00808', '-0.04578', '0.04703', '-0.1388', '-0.0082', '0.133', '-0.081', '-0.07086', '-0.013374', '0.01314', '0.02576', '-0.012024', '-0.0384', '-0.08716', '0.01945', '-0.045', '-0.0574', '-0.2352', '-0.003342', '-0.04318', '0.1417', '-0.02429', '-0.0135', '-0.03442', '0.01211', '-0.01814', '0.01857', '-0.1075', '0.1165', '0.04282', '0.1741', '0.0802', '-0.01834', '-0.10254', '-0.0004869', '-0.03632', '-0.03035', '-0.1545', '0.03827', '-0.1023', '0.0239', '-0.0314', '-0.01241', '-0.1208', '0.01456', '0.02483', '0.01604', '0.07434', '0.001514', '-0.1154', '-0.01619', '-0.00942', '-0.10596', '0.003782', '0.1356', '-0.0343', '-0.16', '0.04492', '0.05673', '0.0547', '0.066', '0.02374', '0.0808', '0.05432', '0.138', '0.04663', '-0.154', '0.109', '-0.06744', '0.0001496', '0.003273', '-0.0931', '0.0846', '0.05276', '0.06107', '-0.01643', '-0.0809', '-0.0306', '-0.03186', '0.0371', '-0.0445', '0.0812', '-0.00368', '-0.01555', '0.068', '0.1746', '0.1368', '-0.00722', '0.0924', '0.11', '-0.02362', '0.000604', '0.2705', '0.0866', '0.1024', '-0.199', '-0.00247', '0.02773']",,,C567581,,,,
mondo:0010433,"systemic lupus erythematosus, susceptibility to, 15","['SLEB15', 'systemic lupus erythematosus, susceptibility to, 15']",,300809,,,,,,,,,,
mondo:0010434,synovial sarcoma,"['Synovialosarcoma', 'synovial sarcoma (disease)', 'sarcoma, synovial, malignant', 'SS', 'sarcoma, synovial', 'synovial sarcoma']",5485,300813,3273,C0039101,,C3400,0001376,D013584,171.9,,10042863,0012570
mondo:0010435,"nystagmus 6, congenital, X-linked","['NYSTAGMUS 6, congenital, X-linked', 'nystagmus 6, congenital, X-linked', 'NYS6', 'nystagmus 6, congenital, X-linked, X-linked recessive']",0111795,300814,,C3151752,"['-0.06107', '0.08844', '0.0363', '-0.0292', '0.065', '-0.1228', '0.0002015', '0.1453', '-0.09326', '-0.09607', '-0.03152', '0.02185', '-0.008', '-0.01312', '-0.03668', '-0.021', '0.04645', '-0.05685', '-0.04852', '-0.184', '-0.03693', '-0.005386', '0.04794', '-0.04172', '0.01964', '-0.03455', '-0.05386', '-0.03818', '0.02736', '-0.0632', '0.10724', '0.00691', '0.1262', '0.04486', '0.00676', '-0.04675', '-0.04007', '-0.09766', '-0.0451', '-0.0913', '0.0652', '-0.11707', '0.002113', '-0.00942', '-0.03613', '-0.0891', '-0.04404', '0.0709', '-0.01836', '0.01526', '-0.0712', '-0.01531', '-0.03192', '-0.0683', '-0.02554', '-0.03787', '0.149', '-0.01211', '-0.11847', '0.01581', '0.04303', '0.0349', '0.002811', '0.0668', '-0.01281', '-0.003687', '0.1553', '0.1361', '-0.12256', '0.08405', '-0.0989', '0.02303', '0.02281', '-0.09546', '0.0979', '0.02527', '0.03119', '-0.05106', '-0.0834', '-0.05792', '0.02426', '-0.03745', '0.0385', '0.1255', '-0.00597', '0.0223', '0.0332', '0.1315', '0.082', '0.02782', '0.07654', '0.1456', '0.04822', '0.0465', '0.2335', '0.04422', '0.1112', '-0.14', '0.03384', '0.008194']",,,,,,,
mondo:0010436,chromosome Xq28 duplication syndrome,['chromosome Xq28 duplication syndrome'],,300815,,C2749007,,,,C567580,,,,
mondo:0010437,severe X-linked mitochondrial encephalomyopathy,"['encephalomyopathy, mitochondrial, X-linked', 'mitochondrial encephalomyopathy due to COXPD6', 'combined oxidative phosphorylation deficiency 6, X-linked recessive', 'combined oxidative phosphorylation deficiency type 6', 'mitochondrial encephalomyopathy due to combined oxidative phosphorylation defect 6', 'COXPD6', 'combined oxidative phosphorylation deficiency 6']",0111502,300816,238329,C4302745,"['-0.691', '0.2284', '0.02776', '-0.09906', '0.2096', '-0.676', '-0.04507', '0.602', '-0.4617', '-0.04385', '-0.0475', '-0.06616', '0.0238', '-0.2979', '0.269', '-0.08234', '-0.05527', '0.07446', '-0.7485', '-0.654', '0.2079', '-0.3582', '0.2876', '-0.101', '0.1787', '-0.2822', '0.2407', '0.06232', '-0.2244', '-0.3994', '0.1348', '0.5566', '0.4373', '-0.1461', '-0.2167', '-0.4927', '-0.0977', '-0.14', '-0.1697', '-0.1015', '-0.1342', '-0.653', '-0.3408', '0.1392', '-0.4114', '-0.2756', '-0.1976', '-0.01913', '-0.02359', '0.0738', '-0.2683', '-0.0971', '-0.07605', '-0.06354', '-0.0265', '-0.5464', '0.3794', '0.0982', '-0.269', '0.3809', '0.006752', '-0.02226', '0.4521', '0.0761', '-0.311', '-0.001095', '0.03732', '0.487', '-0.606', '-0.04913', '-0.2244', '-0.1251', '0.1192', '0.2742', '0.08527', '0.01872', '0.1343', '0.1755', '-0.1671', '0.396', '0.364', '-0.1704', '0.1313', '0.4478', '0.2109', '0.2106', '0.3184', '0.5513', '0.456', '0.0001944', '0.583', '0.24', '-0.1237', '-0.007', '0.6875', '0.5703', '0.3772', '-0.2883', '0.01243', '0.01283']",,,,,,,
mondo:0010438,paroxysmal nocturnal hemoglobinuria 1,"['paroxysmal nocturnal hemoglobinuria 1', 'paroxysmal nocturnal hemoglobinuria caused by mutation in pIgA', 'PIGA paroxysmal nocturnal hemoglobinuria', 'paroxysmal nocturnal hemoglobinuria, somatic', 'PNH1', 'paroxysmal nocturnal hemoglobinuria type 1', 'pIgA paroxysmal nocturnal hemoglobinuria']",,300818,,C3806670,,,,,,,,
mondo:0010439,"cardiomyopathy, fatal fetal, due to myocardial calcification","['cardiomyopathy, fatal fetal, due to myocardial calcification', 'myocardial calcifications resulting in intrauterine foetal death', 'myocardial calcifications resulting in intrauterine fetal death']",,606163,,C1853577,,,,C543241,,,,
mondo:0010440,"autism, susceptibility to, X-linked 4","['X-linked susceptibility to autism-4', 'chromosome Xp22 deletion syndrome', 'susceptibility to autism, X-linked', 'susceptibility to X-linked autism 4', 'AUTSX4', 'autism, susceptibility to, X-linked 4, X-linked recessive', 'autism, susceptibility to, X-linked 4', 'autism, susceptibility to, X-linked type 4']",,300830,,,,,,,,,,
mondo:0010441,CK syndrome,"['mental retardation, X-linked, with thin body habitus and cortical malformation', 'intellectual disability, X-linked, with thin body habitus and cortical malformation', 'CK syndrome, X-linked recessive', 'X-linked intellectual disability-microcephaly-cortical malformation-thin habitus syndrome', 'CK syndrome']",0111898,300831,251383,C3151781,"['-0.449', '0.163', '0.5283', '-0.5264', '0.05005', '-0.4233', '-0.09735', '0.3325', '-0.926', '-0.2096', '-0.236', '-0.3494', '0.2588', '-0.5337', '-0.1181', '0.1113', '0.4324', '-0.05725', '-0.1093', '-0.4922', '0.14', '0.0753', '0.004753', '0.2258', '0.278', '-0.1741', '0.00615', '-0.1256', '0.2322', '-0.2617', '0.2573', '0.1598', '0.8857', '0.301', '0.192', '0.05856', '-0.3088', '-0.11475', '-0.06854', '-0.9756', '0.2559', '-0.2449', '-0.2482', '-0.2715', '-0.04483', '-0.4521', '0.381', '0.4402', '0.0699', '0.09924', '-0.3423', '0.352', '-0.1536', '0.03592', '-0.372', '0.089', '0.253', '0.0912', '-0.1094', '0.4016', '-0.03558', '0.2534', '-0.1685', '0.0339', '-0.2394', '0.2241', '0.1997', '0.3967', '-0.201', '0.3801', '-0.2957', '0.3933', '-0.003521', '-0.1774', '-0.6367', '0.167', '0.4377', '-0.1809', '-0.13', '0.013336', '0.4011', '0.1021', '-0.005173', '0.73', '0.1207', '0.1947', '-0.518', '0.465', '0.2286', '0.7114', '-0.0192', '0.44', '0.3533', '0.2399', '0.429', '0.1924', '0.662', '-0.162', '0.4521', '0.5283']",,,,,,,
mondo:0010442,"46,XX sex reversal 3","['46XX sex reversal 3, X-linked dominant', '46,XX SEX reversal 3', '46,XX Sex reversal, Sox3-related', 'chromosome Xq26 Duplication syndrome', '46,XX Sex reversal type 3', 'SRXX3', '46,XX sex reversal 3', 'chromosome Xq26 deletion syndrome']",0111762,300833,,C3151782,,,,,,,,
mondo:0010443,"macular degeneration, X-linked atrophic","['macular degeneration, X-linked atrophic', 'macular degeneration, X-linked atrophic, X-linked recessive']",0112157,300834,,C3151784,,,,,,,,
mondo:0010444,X-linked dyserythropoetic anemia with abnormal platelets and neutropenia,"['XLANP', 'anemia, X-linked, with or without neutropenia and/or platelet abnormalities', 'anemia, X-linked, with/without neutropenia and/or platelet abnormalities, X-linked recessive']",0112156,300835,363727,,"['-0.4563', '0.362', '0.04425', '0.3523', '0.52', '0.2961', '-0.4592', '0.4902', '-0.2722', '-0.4626', '0.7354', '0.01371', '0.2502', '0.373', '-1.28', '-0.07904', '-0.607', '0.2886', '-0.59', '-0.471', '0.0017805', '-0.528', '0.4714', '-0.2417', '0.7627', '-0.2192', '-0.07465', '-0.3223', '0.456', '0.1465', '0.2812', '0.03003', '0.4468', '0.669', '0.337', '-0.4182', '-0.8564', '-0.778', '0.5854', '-0.2795', '-0.809', '0.4421', '0.002565', '-0.5464', '-0.632', '-0.9253', '0.1752', '0.2109', '0.477', '-0.503', '0.4788', '0.529', '0.826', '-0.198', '0.525', '-0.4922', '-0.05008', '0.3364', '-1.05', '0.1222', '0.0211', '0.3242', '-0.1605', '-0.2644', '0.0008197', '0.4465', '0.1908', '0.962', '-0.5356', '0.833', '0.862', '-0.397', '-0.4648', '-0.673', '0.3054', '0.836', '0.317', '0.389', '0.1404', '0.3516', '0.2253', '-0.02586', '0.0647', '0.06976', '0.4233', '-0.3933', '-0.5854', '0.609', '0.737', '-0.2307', '0.6377', '0.2576', '-0.309', '0.1708', '0.7085', '0.9863', '0.1296', '-0.0924', '0.3887', '-0.4648']",,,,,,,
mondo:0010446,X-linked cone dysfunction syndrome with myopia,"['BORNHOLM eye disease', 'myopia, high, with nonprogressive cone dysfunction', 'Bornholm eye disease', 'Bornholm eye disease, X-linked recessive', 'bed']",,300843,90001,C3159311,,,,C564092,,,,
mondo:0010447,"intellectual disability, X-linked 19","['intellectual disability, X-linked type 19', 'mental retardation, X-linked type 19', 'intellectual developmental disorder, X-linked 19, X-linked dominant', 'intellectual disability, X-linked 19', 'RPS6KA3 non-syndromic X-linked intellectual disability', 'MRX19', 'non-syndromic X-linked intellectual disability caused by mutation in RPS6KA3', 'mental retardation, X-linked 19']",0112019,300844,,C0796225,,,,C563141,,,,
mondo:0010448,moyamoya angiopathy-short stature-facial dysmorphism-hypergonadotropic hypogonadism syndrome,"['syndromic Moyamoya disease', 'Moyamoya disease-short stature-facial dysmorphism-hypergonadotropic hypogonadism', 'chromosome Xq28 deletion syndrome, 3.4-Kb', 'MYMY4', 'Moyamoya disease 4 with short stature, hypergonadotropic hypogonadism, and facial dysmorphism', 'moyamoya disease 4, X-linked recessive']",,300845,280679,C3151857,,,,,,,,
mondo:0010449,"autism, susceptibility to, X-linked 5","['autism, susceptibility to, X-linked 5', 'AUTSX5', 'susceptibility to X-linked autism 5', 'autism, susceptibility to, X-linked type 5']",,300847,,,,,,,,,,
mondo:0010450,"intellectual disability, X-linked 89","['mental retardation, X-linked 89, X-linked dominant', 'intellectual disability, X-linked 89', 'mental retardation, X-linked 89', 'MRX89']",0112031,300848,,,,,,C564036,,,,
mondo:0010451,"intellectual disability, X-linked 41","['intellectual disability, X-linked 41', 'non-syndromic X-linked intellectual disability caused by mutation in GDI1', 'intellectual disability, X-linked 48', 'mental retardation, X-linked type 41', 'MRX41', 'mental retardation, X-linked 48', 'GDI1 non-syndromic X-linked intellectual disability', 'mental retardation, X-linked 41', 'intellectual developmental disorder, X-linked 41, X-linked dominant', 'intellectual disability, X-linked type 41']",0112058,300849,,C3887939,,,,,,,,
mondo:0010452,"intellectual disability, X-linked 90","['non-syndromic X-linked intellectual disability caused by mutation in DLG3', 'intellectual developmental disorder, X-linked 90, X-linked recessive', 'mental retardation, X-linked type 90', 'mental retardation, X-linked 90', 'MRX90', 'intellectual disability, X-linked 90', 'intellectual disability, X-linked type 90', 'DLG3 non-syndromic X-linked intellectual disability']",0112041,300850,,C3275443,,,,,,,,
mondo:0010453,"intellectual disability, X-linked 92","['mental retardation, X-linked 92, X-linked recessive', 'MRX92', 'mental retardation, X-linked 92', 'intellectual disability, X-linked 92']",0112032,300851,,C1845144,,,,C564483,,,,
mondo:0010454,"intellectual disability, X-linked 88","['mental retardation, X-linked 88', 'intellectual disability, X-linked 88', 'intellectual disability, XMEN-linked 88', 'MRX88']",0112053,300852,,C3275444,,,,,,,,
mondo:0010455,"X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia","['X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection, and neoplasia', 'XMEN', 'immunodeficiency, X-linked, with magnesium defect, Epstein-Barr virus infection and neoplasia, X-linked recessive', 'immunodeficiency, X-linked, with magnesium defect, Epstein-Barr VIRUS infection, and neoplasia', 'X-linked magnesium deficiency with Epstein-Barr virus infection and neoplasia', 'combined immunodeficiency due to MAGT1 deficiency', 'Cid due to MAGT1 deficiency']",0080319,300853,317476,C3275445,"['-0.344', '0.1442', '0.2893', '-0.6714', '-0.12256', '-0.1763', '0.1782', '0.02197', '0.1957', '-0.2496', '0.3042', '0.0528', '-0.05005', '-0.1414', '-0.00869', '-0.1781', '-0.00655', '0.2461', '-0.1709', '-0.2231', '-0.08', '-0.2208', '0.587', '-0.295', '0.2354', '-0.1273', '-0.0272', '-0.2339', '-0.1055', '-0.7114', '0.1536', '0.569', '0.6567', '0.02863', '0.10657', '-0.1173', '-0.6064', '-0.1432', '-0.372', '-0.5146', '-0.1469', '-0.2214', '0.09894', '-0.4116', '-0.4727', '-0.6187', '0.03232', '-0.06946', '0.06158', '-0.006466', '-0.2064', '-0.07996', '0.107', '0.03784', '-0.524', '0.2588', '0.075', '-0.626', '-0.303', '0.1383', '0.00982', '0.395', '-0.01646', '0.3489', '0.4373', '-0.07275', '0.374', '0.1195', '-0.495', '0.7056', '-0.2861', '0.1555', '-0.05188', '-0.11017', '0.352', '0.08984', '0.2345', '-0.011185', '0.2074', '0.181', '-0.4167', '-0.01399', '-0.166', '-0.0407', '-0.1081', '0.03293', '0.2444', '0.0533', '0.06726', '-0.07916', '0.1306', '0.3066', '0.0819', '-0.07336', '0.581', '0.68', '0.2316', '-0.6304', '-0.2493', '-0.02135']",C126336,,,,,,
mondo:0010456,"renal cell carcinoma, Xp11-associated","['renal cell carcinoma, papillary, 1', 'renal cell carcinoma, Xp11-associated', 'RCCX1']",,300854,,C3275446,,,,,,,,
mondo:0010457,Ogden syndrome,"['premature ageing appearance-developmental delay-cardiac arrhythmia syndrome', 'X-linked malformation and infantile lethality syndrome', 'N-terminal acetyltransferase deficiency', 'N-alpha-acetyltransferase', 'N acetyltransferase deficiency', 'arylamine n-acetyltransferase 1', 'NAT1 deficiency', 'Acetyl-CoA:arylamine n-acetyltransferase', 'Ogden syndrome', 'N acetyltransferase 1 deficiency', 'premature aging appearance-developmental delay-cardiac arrhythmia syndrome', 'Ogden syndrome, X-linked recessive, X-linked dominant', 'OGDNS']",0050781,300855,276432,C3275447,"['-0.615', '0.1707', '0.4688', '0.05334', '0.6475', '-0.8965', '-0.01437', '0.8154', '-0.8193', '-0.1403', '-0.3328', '-0.0764', '0.3972', '-0.3223', '-0.08905', '0.1582', '0.4517', '-0.2423', '-0.4424', '-0.646', '0.1929', '-0.07446', '0.37', '-0.11584', '0.2815', '-0.1622', '0.02055', '0.2325', '0.4324', '-0.424', '0.7505', '-0.08673', '0.437', '0.2678', '0.0815', '-0.1887', '-0.5146', '0.2551', '0.1176', '-0.261', '-0.1788', '-0.292', '-0.27', '0.4182', '0.3743', '-0.2866', '-0.1901', '0.4456', '-0.0745', '0.1517', '-0.5586', '0.529', '-0.288', '0.4287', '-0.2065', '-0.3015', '-0.1606', '-0.1917', '0.05902', '0.1442', '0.187', '0.1508', '-0.4248', '-0.1366', '0.091', '0.1053', '-0.1353', '0.587', '-0.2264', '-0.04156', '-0.7793', '0.1656', '0.3367', '0.4094', '-0.4375', '-0.2284', '0.3462', '-0.05817', '-0.4033', '-0.2617', '0.06223', '-0.0941', '-0.2297', '0.2454', '0.1842', '0.1598', '-0.1172', '0.3267', '0.4282', '0.2622', '0.164', '0.1655', '0.2009', '0.1686', '0.5625', '0.11334', '0.3457', '-0.1483', '0.3623', '0.1622']",C188215,,C536107,,,,
mondo:0010458,"hypospadias 4, X-linked","['hypospadias 4, X-linked, susceptibility to', 'HYSP4']",,300856,,,,,,,,,,
mondo:0010459,amyotrophic lateral sclerosis type 15,"['UBQLN2 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis 15, with or without frontotemporal dementia', 'amyotrophic lateral sclerosis 15 with or without frontotemporal dementia', 'amyotrophic lateral sclerosis caused by mutation in UBQLN2', 'ALS15', 'amyotrophic lateral sclerosis 15', 'amyotrophic lateral sclerosis 15, with or without frontotemporal dementia, X-linked dominant']",0060206,300857,,C3275459,,,,,,,,
mondo:0010460,syndromic X-linked intellectual disability 17,"['intellectual disability, X-linked, with alacrima and achalasia', 'MRXS17', 'intellectual disability, X-linked, syndromic 17', 'mental retardation, X-linked, with alacrima and achalasia', 'mental retardation, X-linked, syndromic 17', 'mental retardation, X-linked, syndromic 17, X-linked recessive', 'intellectual disability-alacrima-achalasia syndrome', 'X-linked intellectual disability with alacrima and achalasia', 'X-linked mental retardation with alacrima and achalasia', 'syndromic X-linked intellectual disability type 17']",0060803,300858,289483,C3275460,,,,,,,,
mondo:0010461,syndromic X-linked intellectual disability Nascimento type,"['intellectual disability, X-linked, syndromic 30', 'intellectual developmental disorder, X-linked syndromic, Nascimento type, X-linked recessive', 'X-linked intellectual disability-nail dystrophy-seizures syndrome', 'intellectual disability, X-linked, syndromic, Nascimento type', 'mental retardation, X-linked, syndromic 30', 'X-linked intellectual disability, Nascimento type', 'MRXSN', 'intellectual disability, X-linked syndromic, Nascimento-type', 'mental retardation, X-linked, syndromic, Nascimento type', 'mental retardation, X-linked syndromic, Nascimento-type']",0060820,300860,163956,C3275464,"['-0.1932', '0.2336', '0.4248', '-0.65', '0.1385', '-0.2974', '-0.00802', '0.377', '-0.627', '-0.1709', '0.05188', '-0.00806', '0.299', '-0.1833', '-0.166', '0.1796', '0.74', '-0.07184', '-0.05664', '-0.2607', '-0.1098', '0.02325', '-0.02864', '-0.113', '0.0822', '-0.1526', '-0.2235', '0.03207', '0.3525', '-0.503', '0.3562', '-0.1333', '0.3599', '0.2595', '0.2145', '0.1326', '-0.1986', '-0.401', '-0.242', '-0.7505', '0.4358', '-0.3352', '-0.3428', '-0.1545', '-0.2081', '-0.4102', '0.3176', '0.3462', '-0.04846', '0.16', '-0.4573', '0.1635', '-0.1665', '0.11395', '-0.286', '-0.02972', '0.003365', '-0.09985', '-0.1466', '-0.0759', '-0.2625', '0.0876', '-0.5576', '0.1935', '-0.0723', '0.0169', '0.334', '0.2676', '-0.0944', '0.4246', '-0.3228', '0.2339', '0.1633', '-0.10345', '-0.2482', '0.232', '0.1785', '-0.4424', '-0.311', '-0.064', '0.04642', '-0.2925', '-0.1357', '0.3904', '0.0763', '0.213', '-0.2201', '0.5176', '0.4028', '0.3137', '0.02907', '0.4958', '0.5464', '0.3696', '0.72', '0.03625', '-0.00438', '-0.2656', '0.5566', '0.287']",,,,,,,
mondo:0010462,syndromic X-linked intellectual disability Chudley-Schwartz type,"['X-linked intellectual disability with seizures, hypogammaglobinemia, and gait disturbance', 'intellectual disability, X-linked, with seizures, hypogammaglobulinemia, and Gait disturbance', 'X-linked mental retardation with seizures, hypogammaglobinemia, and gait disturbance', 'mental retardation, X-linked, syndromic, Chudley-Schwartz type', 'mental retardation, X-linked, with seizures, hypogammaglobulinemia, and Gait disturbance', 'mental retardation, X-linked, syndromic, Chudley-Schwartz type, X-linked recessive', 'MRXSCS', 'intellectual disability, X-linked, syndromic, Chudley-Schwartz type']",0060819,300861,,C3275471,,,,,,,,
mondo:0010463,"X-linked dominant chondrodysplasia, Chassaing-Lacombe type","['X-linked dominant chondrodysplasia-hydrocephaly-microphthalmia syndrome', 'chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia', 'chondrodysplasia with platyspondyly, distinctive brachydactyly, hydrocephaly, and microphthalmia, X-linked dominant']",0112106,300863,163966,C3275476,"['-0.839', '0.3994', '0.3367', '-0.3845', '0.3726', '-0.621', '-0.2437', '0.766', '-0.813', '-0.6387', '-0.2808', '0.711', '0.0743', '0.11847', '0.494', '-0.1223', '0.4539', '-0.07904', '-0.3071', '-0.05276', '-0.3008', '-0.04913', '0.6353', '-0.4253', '0.524', '0.1564', '-0.4707', '0.05066', '0.3484', '-0.5186', '0.4963', '0.06964', '0.1135', '0.03026', '0.5205', '-0.2927', '-0.2874', '-0.514', '-0.38', '0.1879', '0.1724', '-0.010185', '0.08386', '0.00363', '0.07007', '-0.459', '0.02913', '0.173', '-0.12305', '-0.3252', '-0.2832', '-0.4978', '-0.237', '-0.01794', '-0.7812', '-0.6646', '0.5464', '0.04227', '0.3984', '0.3223', '0.10236', '-0.05215', '-0.4285', '0.5083', '0.1715', '-0.0886', '0.04868', '-0.0406', '-0.417', '-0.01506', '-0.11615', '0.3496', '0.39', '0.09845', '-0.298', '0.0194', '-0.2632', '0.09314', '-0.1844', '-0.3474', '-0.3171', '-0.1027', '0.2074', '0.218', '0.442', '0.1511', '-0.3381', '0.3486', '0.3813', '-0.0697', '-0.3586', '0.3254', '0.06586', '-0.2174', '0.784', '0.5527', '0.5317', '-0.656', '0.6787', '0.2468']",,,,,,,
mondo:0010464,X-linked cerebral-cerebellar-coloboma syndrome syndrome,"['cerebral-cerebellar-coloboma syndrome, X-linked, X-linked recessive', 'cerebral-cerebellar-coloboma syndrome, X-linked', 'X-linked intellectual disability, Kroes type', 'X-linked cerebral-cerebellar-coloboma syndrome']",,300864,163961,C3275487,,,,,,,,
mondo:0010465,Kabuki syndrome 2,"['Kabuki syndrome type 2', 'KABUK2', 'Kabuki syndrome 2, X-linked dominant', 'KABUKI syndrome 2', 'Kabuki syndrome 2']",,300867,,C3275495,,,,,,,,
mondo:0010466,multiple congenital anomalies-hypotonia-seizures syndrome 2,"['multiple congenital anomalies-hypotonia-seizures syndrome type 2', 'DEE20', 'multiple congenital anomalies/dysmorphic syndrome-intellectual disability caused by mutation in PIGA', 'developmental and epileptic encephalopathy 20', 'glycosylphosphatidylinositol biosynthesis defect 4', 'multiple congenital anomalies-hypotonia-seizures syndrome 2, X-linked recessive', 'PIGA multiple congenital anomalies/dysmorphic syndrome-intellectual disability', 'MCAHS type 2', 'GPIBD4', 'multiple congenital anomalies-hypotonia-seizures syndrome 2', 'MCAHS2', 'epileptic encephalopathy, early infantile, 20']",0080139,300868,300496,C3275508,"['0.0351', '-0.0776', '-0.1763', '0.2491', '-0.3855', '-0.259', '0.586', '0.3696', '-0.5073', '-0.3435', '-0.1004', '-0.4512', '0.00211', '0.565', '-0.73', '0.1937', '-0.189', '0.0149', '-0.004074', '-0.3547', '0.3254', '1.098', '0.02094', '-0.1162', '-0.02965', '-0.2362', '0.012146', '0.1448', '-0.05792', '0.3987', '-0.03093', '0.02669', '0.2482', '0.1019', '0.612', '0.29', '-0.0293', '-0.3137', '0.03308', '-0.6685', '-0.00603', '-0.07697', '-0.2761', '-0.2983', '0.0759', '-0.2979', '0.1571', '0.925', '0.11633', '0.562', '-0.1781', '0.1356', '0.2622', '-0.753', '-0.256', '0.0556', '-0.3398', '-0.01837', '0.0313', '-0.1263', '-0.3015', '0.55', '0.4363', '0.1718', '-0.68', '0.8394', '0.3672', '-0.1277', '-0.713', '0.9023', '0.251', '0.7334', '0.2502', '-0.348', '0.08386', '0.6855', '0.901', '0.2045', '-0.2037', '0.00804', '0.1061', '0.8755', '0.4624', '0.2905', '0.402', '0.10583', '-0.218', '0.812', '0.306', '1.038', '-0.0342', '0.4539', '0.4634', '0.11816', '0.0737', '-0.00721', '0.2778', '-0.3743', '0.4028', '0.5923']",,,,,,,
mondo:0010467,Xq27.3q28 duplication syndrome,"['trisomy Xq27.3-q28', 'dup(X)(q27.3q28)', 'chromosome xq27.3-q28 duplication syndrome, X-linked recessive', 'Xq27.3-q28 microduplication syndrome', 'chromosome Xq27.3-q28 DUPLICATION syndrome', 'trisomy Xq27.3q28']",,300869,261483,C3275521,,,,,,,,
mondo:0010468,"aneurysm, intracranial berry, 5","['ANIB5', 'aneurysm, intracranial BERRY, 5']",0080968,300870,,C1835857,,,,C563670,,,,
mondo:0010469,epsilon-trimethyllysine hydroxylase deficiency,"['epsilon-trimethyllysine hydroxylase deficiency', 'susceptibility to X-linked autism 6', 'TMLHED', 'autism, susceptibility to, X-linked 6', 'AUTSX6', 'autism, susceptibility to, X-linked 6, X-linked recessive', 'EPSILON-trimethyllysine HYDROXYLASE deficiency']",,300872,,C3550875,,,,,,,,
mondo:0010471,Cornelia de Lange syndrome 5,"['Cornelia de Lange syndrome 5, X-linked dominant', 'Cornelia De Lange syndrome type 5', 'Cornelia de Lange syndrome 5', 'CDLS5', 'Cornelia DE Lange syndrome 5']",0080509,300882,,C3550903,,,,,,,,
mondo:0010472,"developmental and epileptic encephalopathy, 36","['developmental and epileptic encephalopathy 36', 'DEE36', 'EIEE36', 'ALG13-CDG', 'congenital disorder of glycosylation type Is', 'congenital disorder of glycosylation type 1s', 'epileptic encephalopathy, early infantile, 36', 'CDG1S', 'CDG-Is', 'CDG Is', 'congenital disorder of glycosylation, type Is', 'CDG syndrome type Is']",0080470,300884,324422,C3550904,"['-0.2847', '0.127', '0.11536', '-0.4204', '0.04874', '-0.314', '-0.0875', '0.1556', '-0.454', '-0.1041', '-0.06604', '-0.05908', '0.03687', '-0.3274', '-0.3071', '0.02646', '0.3523', '-0.000556', '-0.138', '-0.615', '0.2668', '-0.132', '0.1877', '-0.1501', '0.06012', '-0.02235', '-0.06055', '0.10706', '-0.01132', '-0.1405', '0.08734', '0.2417', '0.4788', '0.0822', '-0.2588', '0.1558', '-0.449', '-0.0555', '-0.324', '-0.1364', '-0.04706', '-0.2961', '0.02283', '0.02745', '-0.2439', '0.0844', '-0.0717', '0.0312', '0.4932', '0.3555', '-0.2556', '0.08453', '0.1024', '0.1528', '-0.1593', '-0.274', '0.2373', '0.1501', '-0.5044', '0.3774', '0.03848', '0.1482', '0.135', '-0.1444', '0.11694', '0.00946', '0.04883', '0.01785', '-0.522', '0.3455', '-0.2874', '0.1127', '0.3025', '-0.1572', '0.2167', '-0.11414', '0.696', '0.11847', '-0.0642', '0.2961', '-0.27', '-0.1718', '-0.04288', '0.1052', '-0.013435', '-0.00921', '0.05234', '0.525', '0.4546', '0.138', '-0.1117', '0.5273', '0.10266', '0.01564', '0.244', '0.8286', '0.4827', '-0.3276', '0.1953', '0.1868']",,,,,,,
mondo:0010473,X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome,"['mental retardation, X-linked, syndromic type 32', 'intellectual developmental disorder, X-linked syndromic 32, X-linked recessive', 'MRXS32', 'mental retardation, X-linked, syndromic 32', 'intellectual disability, X-linked, syndromic 32', 'intellectual disability, X-linked, syndromic type 32']",0060828,300886,324410,C3550913,"['0.02184', '-0.1034', '0.2426', '-0.012215', '0.494', '-0.67', '0.2932', '0.6074', '-0.4165', '-0.471', '0.3413', '-0.04294', '0.3794', '0.6416', '-0.6006', '-0.4985', '-0.8335', '0.1256', '-0.1919', '-0.8315', '0.3328', '0.4888', '-0.348', '-0.11835', '0.1404', '-0.673', '0.05765', '0.34', '0.511', '-0.2203', '0.6987', '0.1231', '0.7847', '0.10803', '-0.279', '-0.485', '-0.0617', '-0.0954', '0.921', '-0.557', '0.128', '0.3022', '-0.281', '0.0828', '-0.03827', '0.2734', '0.2437', '-0.3208', '0.0474', '-0.0447', '-0.5566', '0.566', '0.4895', '-0.03415', '-0.2291', '0.1589', '-0.383', '0.2323', '-0.4773', '-0.3013', '-0.3801', '0.3254', '0.311', '-0.513', '-0.04172', '-0.3289', '0.1354', '0.507', '-0.7285', '0.1865', '0.1289', '0.5073', '0.4763', '-0.5977', '0.2727', '0.3418', '0.1722', '0.147', '-0.1868', '0.474', '-0.011986', '-0.262', '-0.10956', '-0.04688', '0.3638', '0.02596', '0.271', '0.4385', '-0.0442', '0.463', '-0.11743', '-0.2131', '-0.3706', '0.5796', '0.5967', '0.3376', '-0.3394', '-0.2286', '-0.071', '-0.1404']",,,,,,,
mondo:0010474,linear skin defects with multiple congenital anomalies 2,"['linear skin defects with multiple congenital anomalies 2, X-linked dominant', 'linear skin defects with multiple congenital anomalies 2', 'aplasia cutis congenita, Reticulolinear, with microcephaly, Facial Dysmorphism, and Other congenital anomalies', 'linear skin defects with multiple congenital anomalies type 2', 'LSDMCA2', 'microphthalmia with linear skin defects syndrome caused by mutation in COX7B', 'COX7B microphthalmia with linear skin defects syndrome']",0111877,300887,,C3550921,,,,,,,,
mondo:0010475,X-linked central congenital hypothyroidism with late-onset testicular enlargement,"['hypothyroidism, central, and testicular enlargement, X-linked recessive', 'hypothyroidism, central, and testicular enlargement', 'Immunoglobulin superfamily member 1 deficiency syndrome', 'central hypothyroidism and testicular enlargement', 'CHTE', 'IGSF1 deficiency syndrome', 'X-linked central congenital hypothyroidism with late-onset macroorchidism', 'X-linked central congenital hypothyroidism with late-onset testicular enlargement', 'hypothyroidism Central and testicular enlargement']",0111140,300888,329235,C3550963,"['-0.8516', '0.4678', '-0.002838', '-0.3853', '0.463', '-0.2109', '-0.1842', '0.1747', '-0.691', '-0.6045', '0.0554', '0.1832', '0.268', '0.01119', '0.00585', '-0.2532', '0.2196', '-0.02321', '-0.2556', '-0.5464', '0.0913', '-0.4724', '-0.04135', '-0.4958', '0.1696', '-0.1211', '0.1492', '-0.1401', '0.247', '-0.84', '0.659', '0.539', '0.399', '-0.06354', '-0.514', '-0.01134', '0.0495', '-0.239', '-0.309', '-0.0482', '0.6147', '0.2964', '0.2769', '0.4387', '-0.1802', '-0.504', '0.4043', '-0.2668', '0.3467', '0.2864', '0.1273', '0.2439', '-0.1554', '0.048', '-0.1505', '0.08093', '0.51', '-0.44', '-0.5483', '0.6084', '0.332', '0.6514', '-0.0964', '-0.0271', '0.267', '0.3442', '0.3916', '0.4622', '-0.5146', '-0.3325', '-0.504', '0.0718', '0.232', '-0.09625', '0.1366', '-0.3433', '0.11346', '0.4753', '-0.3274', '0.295', '0.09924', '-0.11584', '-0.392', '-0.03525', '-0.05826', '-0.2432', '0.2676', '-0.3577', '0.4966', '0.08795', '0.0692', '0.669', '0.1257', '-0.434', '1.041', '0.02556', '0.272', '-0.4148', '0.4844', '0.2325']",C130989,,,,,,
mondo:0010476,neurodegeneration with brain iron accumulation 5,"['SENDA', 'WDR45 neurodegeneration with brain iron accumulation', 'beta-propeller protein-associated neurodegeneration', 'BPAN', 'neurodegeneration with brain iron accumulation caused by mutation in WDR45', 'static encephalopathy Of childhood with neurodegeneration In adulthood', 'static encephalopathy of childhood with neurdegeneration in adulthood', 'neurodegeneration with brain iron accumulation type 5', 'neurodegeneration with brain iron accumulation 5', 'neurodegeneration with brain iron accululation 5', 'neurodegeneration with brain iron accumulation 5, X-linked dominant', 'NBIA5', 'static encephalopathy of childhood with neurodegeneration in adulthood']",0110739,300894,329284,CN168656,"['-0.3484', '0.2554', '0.0804', '-0.321', '0.459', '-0.582', '-0.5254', '0.199', '-0.3467', '0.3452', '-0.6313', '-0.1163', '0.1224', '-0.2637', '0.3552', '-0.4675', '-0.1849', '-0.263', '-0.527', '-0.6167', '-0.009', '-0.3242', '0.2698', '-0.1289', '0.2058', '0.10016', '0.003311', '-0.2578', '-0.2778', '0.1646', '0.0482', '0.1638', '0.4458', '0.1478', '0.1168', '-0.0938', '-0.1018', '-0.3003', '0.12274', '-0.09906', '0.237', '-0.5996', '0.05862', '0.2864', '0.0273', '-0.3015', '0.04926', '-0.05905', '0.02997', '-0.1934', '0.1179', '0.1372', '-0.1992', '0.2542', '0.1454', '-0.1107', '0.5806', '0.07404', '-0.2786', '0.5107', '0.2294', '0.0541', '0.2188', '-0.4578', '0.03568', '0.11615', '0.2544', '0.237', '-0.44', '0.2161', '-0.6177', '-0.01924', '-0.0644', '-0.01116', '0.04886', '-0.10876', '0.0651', '0.3125', '-0.421', '-0.05643', '0.1362', '-0.1737', '-0.1095', '0.286', '0.408', '-0.1804', '0.2318', '0.4558', '0.7656', '0.3337', '0.438', '0.3877', '-0.1244', '-0.1694', '0.06256', '0.1945', '0.632', '-0.09607', '0.4353', '0.0505']",C175210,,,,,,
mondo:0010477,"blepharophimosis - intellectual disability syndrome, MKB type","['blepharophimosis-mental retardation syndrome, Maat-Kievit-Brunner type', 'Ohdo syndrome, X-linked, X-linked recessive', 'BMRS, Maat-Kievit-Brunner type', 'BMRS, MKB type', 'blepharophimosis-intellectual disability syndrome, Maat-Kievit-Brunner type', 'X-linked Ohdo syndrome', 'Ohdo syndrome, X-linked', 'OHDOX']",,300895,293707,C3698541,"['-0.0805', '-0.0514', '0.295', '-0.471', '0.1865', '-0.3604', '0.1373', '0.5513', '-0.6685', '-0.2369', '-0.010315', '-0.1501', '-0.06152', '0.00452', '0.0463', '0.1978', '0.2388', '0.06354', '-0.3938', '-0.3306', '-0.05066', '0.09155', '0.2546', '-0.2917', '0.313', '-0.4375', '-0.2573', '-0.2245', '0.4622', '-0.41', '0.3667', '-0.11584', '0.3147', '0.2974', '0.366', '-0.1407', '-0.215', '-0.3936', '-0.1449', '-0.4136', '0.3794', '-0.001129', '-0.2448', '-0.1467', '0.1907', '-0.4988', '0.2678', '0.4456', '-0.3337', '-0.00991', '-0.4521', '0.08563', '-0.1877', '0.132', '-0.1775', '0.02658', '-0.1488', '-0.0549', '0.1532', '0.191', '0.11444', '0.03894', '-0.03375', '0.3967', '0.00869', '-0.1987', '-0.07965', '0.2173', '-0.3474', '0.47', '-0.495', '0.1443', '-0.1107', '-0.1232', '-0.08905', '0.001634', '0.1483', '0.03665', '-0.571', '0.1203', '0.2627', '-0.1843', '-0.0899', '0.674', '0.02158', '0.1974', '-0.2703', '0.1031', '0.1726', '0.2246', '-0.1154', '0.4978', '0.2368', '0.2864', '0.656', '-0.0787', '0.104', '-0.4934', '0.5654', '0.2328']",,,,759.89,,,
mondo:0010478,SLC35A2-congenital disorder of glycosylation,"['congenital disorder of glycosylation, type IIm, Somatic mosaicism, X-linked dominant', 'CDG-IIm', 'epileptic encephalopathy, early infantile, 22; EIEE22', 'congenital disorder of glycosylation type 2m', 'CDG IIm', 'congenital disorder of glycosylation, type IIm', 'SLC35A2-CDG', 'congenital disorder of glycosylation type IIm', 'CDG2M', 'EIEE22', 'epileptic encephalopathy, early infantile, 22', 'CDG syndrome type IIm']",0070265,300896,356961,C3806688,"['-0.69', '0.0459', '0.01346', '-0.2184', '0.534', '-0.6646', '0.1381', '0.2815', '-0.9854', '0.000265', '-0.3872', '-0.1426', '0.3105', '-0.5977', '-0.349', '0.004635', '0.2607', '-0.747', '-0.8647', '-0.4043', '0.2272', '-0.232', '0.2391', '0.0772', '0.4265', '-0.411', '0.00889', '-0.006157', '0.3054', '-0.05542', '0.303', '0.3127', '0.688', '0.328', '-0.04227', '0.3977', '-0.189', '-0.04123', '-0.0336', '-0.4277', '0.5103', '-0.572', '-0.1696', '0.1016', '-0.1664', '-0.341', '0.1617', '0.56', '0.07245', '-0.1544', '-0.1646', '0.1398', '-0.2301', '0.0788', '-0.3794', '-0.0656', '0.1632', '0.0521', '-0.2932', '0.574', '-0.148', '0.2013', '0.3481', '-0.0369', '-0.4702', '0.2498', '0.686', '0.5356', '-0.581', '0.1041', '-0.5254', '0.2415', '0.0589', '0.1613', '-0.402', '0.01662', '1.069', '-0.496', '-0.1488', '-0.1428', '0.454', '-0.2546', '-0.3013', '0.4778', '0.02551', '-0.0228', '-0.2201', '0.7373', '0.6143', '0.5806', '-0.1192', '0.656', '0.73', '0.1776', '0.2512', '0.2864', '0.6987', '-0.2656', '0.648', '0.4106']",,,,,,,
mondo:0010479,Charcot-Marie-Tooth disease X-linked dominant 6,"['Charcot-Marie-Tooth disease, X-linked dominant, type 6', 'X-linked Charcot-Marie-Tooth disease type 6', 'Charcot-Marie-Tooth disease, X-linked dominant, 6, X-linked dominant', 'Charcot-Marie-Tooth neuropathy, X-linked dominant, 6', 'Charcot-Marie-Tooth disease, X-linked dominant, 6', 'Charcot-Marie-Tooth disease X-linked dominant type 6', 'CMT6X', 'Charcot-Marie-Tooth neuropathy X-linked dominant 6', 'CMTX6']",0110207,300905,352675,C3806702,"['0.1615', '0.1725', '0.4062', '-0.0642', '0.0631', '-0.3232', '0.2194', '0.4714', '-0.6187', '-0.542', '-0.005627', '0.446', '-0.272', '0.4487', '0.06793', '0.1274', '-0.2217', '-0.3809', '-0.7', '-0.5933', '0.1917', '0.6016', '0.173', '0.5654', '0.286', '0.012146', '0.272', '-0.1589', '0.1017', '-0.02904', '0.307', '-0.6826', '0.1681', '0.1831', '0.3782', '-0.8076', '-0.691', '-0.3394', '0.2607', '-0.0514', '-1.356', '-0.55', '-0.2861', '0.3', '0.03552', '-0.3276', '0.04163', '-0.05304', '-0.308', '-0.00964', '-0.04733', '0.3665', '-0.2869', '-1.233', '0.1124', '0.0796', '-0.1681', '0.5635', '-0.628', '-0.289', '-0.06683', '-0.00877', '0.657', '0.688', '-0.92', '1.173', '-0.2345', '0.717', '-0.6226', '0.4255', '-0.6577', '0.08417', '0.457', '-0.1727', '1.089', '0.62', '-0.11835', '0.423', '0.0127', '-0.4546', '-0.1492', '-0.09155', '0.969', '0.546', '0.1024', '0.2046', '0.02063', '0.6143', '0.4402', '0.2764', '0.2384', '0.2279', '0.00346', '0.2664', '0.6147', '0.601', '0.593', '-0.669', '0.18', '0.465']",,,,,,,
mondo:0010480,"anemia, nonspherocytic hemolytic, due to G6PD deficiency","['hemolytic anemia, G6PD deficient (favism), X-linked dominant', 'severe hemolytic anemia due to G6PD deficiency', 'hemolytic anemia due to G6PD deficiency', 'Class I G6PD deficiency', 'class I glucose-6-phosphate dehydrogenase deficiency', 'hemolytic anaemia due to G6PD deficiency', 'anemia, nonspherocytic hemolytic, due to G6PD deficiency', 'severe hemolytic anaemia due to G6PD deficiency']",,300908,466026,C2720289,,,,C567533,,,,
mondo:0010481,angioedema,"['Quincke oedema', 'Quincke edema', 'Edemas, angioneurotic', 'Quincke^s edema', 'angioedemas', 'angioneurotic Edemas', 'giant Urticarias', 'angioneurotic oedema', 'edema, Quincke^s', 'Quinckes edema', 'angioneurotic edema', 'Quincke^s oedema', 'giant urticaria', 'Urticarias, giant', 'edema, angioneurotic', 'urticaria, giant', 'Quinckes oedema']",1558,,,,"['-0.1454', '0.1184', '-0.598', '-0.306', '-0.787', '-0.2324', '-0.1309', '-0.0226', '-0.3208', '0.09265', '0.7573', '0.837', '-0.4436', '0.4146', '-0.7686', '0.2195', '-0.4512', '-0.352', '-0.2876', '-0.2224', '0.2463', '0.03607', '-0.0653', '-0.4595', '-0.002676', '-0.6245', '-0.4573', '-0.145', '0.123', '-0.8174', '0.1956', '-0.276', '-0.1136', '-0.2014', '-0.1667', '0.2069', '-0.6304', '0.2917', '0.1417', '-0.1603', '0.4148', '-0.791', '-0.1846', '-0.2974', '-0.0483', '0.2079', '-0.1284', '0.1497', '0.535', '-0.01551', '-0.7783', '-0.0863', '0.3838', '0.1487', '-0.6177', '-0.1848', '0.066', '0.02939', '-0.512', '-0.257', '-0.2184', '0.3274', '0.02818', '-0.1342', '0.1536', '0.4587', '1.089', '0.4385', '-0.0355', '0.92', '-0.427', '0.1588', '-0.1461', '-0.5625', '0.1383', '0.6875', '0.484', '-0.122', '-0.2407', '-0.032', '-0.2343', '-0.1971', '-0.3333', '-0.2313', '0.2722', '0.2233', '-0.3098', '0.11816', '0.04388', '0.3235', '0.01541', '0.1863', '-0.1915', '0.5854', '0.4685', '0.2456', '-0.425', '-0.3467', '-0.4587', '0.025']",,0005532,D000799,995.1,,,0100665
mondo:0010482,X-linked parkinsonism-spasticity syndrome,"['XPDS', 'PARKINSONISM with spasticity, X-linked', 'Parkinsonism with spasticity, X-linked, X-linked recessive']",0112105,300911,363654,C3806722,"['-0.643', '0.4243', '0.3877', '-0.3633', '-0.2279', '-0.5254', '0.05457', '0.3477', '-0.75', '0.0782', '0.0947', '0.1627', '0.1179', '-0.505', '0.5337', '0.2603', '0.2139', '-0.305', '-0.2272', '-0.889', '0.1608', '0.2808', '0.344', '-0.0699', '0.00849', '0.07983', '0.052', '-0.4468', '-0.5527', '-0.2141', '0.10004', '0.3928', '0.621', '0.2094', '-0.2422', '-0.2046', '-0.10535', '0.0508', '-0.1571', '-0.5327', '0.2137', '-0.04233', '-0.247', '0.2274', '0.517', '-0.777', '-0.09296', '0.4402', '0.01813', '0.3325', '-0.3035', '0.7246', '0.01634', '-0.1892', '-0.04654', '-0.3455', '0.4575', '-0.2013', '-0.1718', '-0.0819', '0.04492', '0.10034', '-0.1516', '-0.1787', '-0.703', '-0.0942', '0.458', '0.1997', '-0.37', '0.3394', '-0.126', '-0.11743', '0.1425', '-0.38', '0.242', '0.2468', '0.2832', '0.059', '-0.1243', '-0.357', '0.2615', '-0.4429', '0.428', '0.54', '-0.0877', '0.2458', '-0.002645', '0.3796', '0.2487', '0.1302', '0.385', '-0.1512', '-0.02357', '0.1757', '0.269', '0.365', '0.4434', '0.09296', '0.128', '0.6123']",,,,,,,
mondo:0010483,"X-linked intellectual disability, Cantagrel type","['MRX98', 'mental retardation, X-linked 98', 'intellectual developmental disorder, X-linked 98, X-linked dominant', 'intellectual disability, X-linked type 98', 'intellectual disability, X-linked 98', 'mental retardation, X-linked type 98']",0112044,300912,85277,C3806730,"['-0.05234', '0.261', '0.3767', '-0.10364', '0.3137', '-0.672', '-0.2761', '0.7896', '-0.919', '-0.1685', '-0.2998', '-0.2144', '0.0405', '-0.3237', '0.6353', '0.1328', '0.2124', '-0.3408', '-0.4155', '-0.5854', '-0.0957', '-0.1437', '0.3074', '-0.5693', '0.2793', '-0.49', '-0.3594', '0.3325', '-0.09924', '-0.3547', '0.2632', '-0.3657', '0.3525', '0.339', '0.08936', '-0.5464', '-0.08154', '-0.0774', '-0.2451', '0.01755', '-0.2676', '-0.51', '-0.4475', '0.1564', '0.0917', '0.001758', '-0.10516', '0.4644', '-0.297', '0.3203', '-0.2898', '0.0976', '-0.496', '-0.3708', '0.1782', '-0.2483', '-0.04706', '0.08636', '-0.2174', '0.3274', '-0.1693', '0.2766', '0.5063', '0.568', '0.02936', '-0.2908', '0.4658', '0.2808', '-0.277', '-0.0004468', '0.2006', '0.4001', '0.0978', '0.1069', '0.3616', '0.06415', '0.2378', '0.2129', '-0.457', '0.05807', '-0.003181', '0.09845', '0.1256', '0.3281', '0.2256', '0.2258', '0.2172', '0.1824', '0.2355', '0.2786', '0.0798', '0.5376', '0.05658', '-0.2156', '0.4507', '0.1947', '-0.03308', '-0.1729', '0.4998', '-0.03053']",,,,,,,
mondo:0010484,"hearing loss, X-linked 6","['deafness, X-linked type 6', 'deafness, X-linked 6, X-linked recessive', 'X-linked nonsyndromic deafness caused by mutation in COL4A6', 'COL4A6 X-linked nonsyndromic deafness', 'deafness, X-linked 6', 'DFNX6']",0111740,300914,,C3806737,,,,,,,,
mondo:0010485,X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome,"['microphthalmia, syndromic type 13', 'colobomatous microphthalmia with microcephaly, short stature, and psychomotor retardation', 'X-linked colobomatous microphthalmia-microcephaly-short stature-psychomotor retardation syndrome', 'microphthalmia, syndromic 13', 'Maine microphthalmos', 'MCOPS13']",0111811,300915,431140,C3806742,,,,,,,,
mondo:0010486,"Olmsted syndrome, X-linked","['palmoplantar keratoderma, mutilating, with periorificial keratotic plaques, X-linked', 'Olmsted syndrome, X-linked, X-linked recessive', 'Olmsted syndrome, X-linked']",0112012,300918,,C3806745,,,,,,,,
mondo:0010487,"intellectual disability, X-linked 99","['mental retardation, X-linked type 99', 'USP9X non-syndromic X-linked intellectual disability', 'MRX99', 'intellectual disability, X-linked 99', 'intellectual disability, X-linked type 99', 'mental retardation, X-linked 99', 'intellectual developmental disorder, X-linked 99, X-linked recessive', 'non-syndromic X-linked intellectual disability caused by mutation in USP9X']",0112026,300919,,C3806746,,,,,,,,
mondo:0010488,"intellectual disability, X-linked 100","['MRX100', 'intellectual developmental disorder, X-linked 100, X-linked recessive', 'mental retardation, X-linked 100', 'intellectual disability, X-linked 100', 'mental retardation, X-linked type 100', 'intellectual disability, X-linked type 100', 'non-syndromic X-linked intellectual disability caused by mutation in KIF4A', 'KIF4A non-syndromic X-linked intellectual disability']",0112040,300923,,C3890167,,,,,,,,
mondo:0010489,"intellectual disability, X-linked 101","['MID2 non-syndromic X-linked intellectual disability', 'intellectual developmental disorder, X-linked 101, X-linked recessive', 'mental retardation, X-linked type 101', 'intellectual disability, X-linked 101', 'mental retardation, X-linked 101', 'intellectual disability, X-linked type 101', 'non-syndromic X-linked intellectual disability caused by mutation in MID2', 'MRX101']",0112048,300928,,C3890168,,,,,,,,
mondo:0010490,SSR4-congenital disorder of glycosylation,"['CDG1Y', 'carbohydrate deficient glycoprotein syndrome type Iy', 'CDG 1Y', 'congenital disorder of glycosylation, type Iy', 'CDG-Iy', 'CDG syndrome type Iy', 'SSR4-CDG', 'congenital disorder of glycosylation type Iy', 'congenital disorder of glycosylation type 1y', 'CDG Iy', 'congenital disorder of glycosylation, type Iy, X-linked recessive', 'CDGIy']",0080574,300934,370927,C4012395,"['-0.2817', '0.2355', '0.781', '-0.275', '0.0476', '-0.4941', '-0.236', '0.4265', '-0.736', '0.0861', '0.06476', '-0.2238', '-0.04398', '-0.506', '-0.1737', '0.1343', '-0.02266', '-0.1656', '-0.598', '-0.839', '-0.09406', '0.2043', '-0.2253', '-0.4934', '0.3528', '-0.3708', '-0.4272', '0.1873', '0.4116', '-0.354', '0.0964', '0.2141', '0.349', '0.1436', '0.08826', '-0.0977', '0.0402', '0.1411', '-0.3347', '-0.4834', '0.0832', '-0.02174', '-0.31', '-0.0464', '-0.3564', '-0.09985', '0.1781', '-0.01877', '0.43', '0.663', '-0.804', '0.3677', '-0.2207', '-0.1533', '0.08405', '-0.1117', '-0.08167', '0.3672', '-0.2047', '0.4507', '0.3425', '0.2773', '-0.0757', '0.02716', '0.1439', '-0.01457', '0.286', '0.004025', '-0.0974', '0.3765', '-0.3794', '0.1613', '0.07135', '0.2283', '-0.08746', '0.2428', '0.574', '-0.483', '-0.3875', '0.4363', '0.003937', '-0.2742', '0.1555', '0.2583', '-0.2242', '0.3074', '0.0505', '0.46', '0.898', '0.1986', '-0.4119', '0.511', '0.2927', '0.2349', '0.2493', '0.5244', '-0.0145', '-0.328', '0.307', '0.2925']",,,,,,,
mondo:0010491,X-linked acrogigantism due to Xq26 microduplication,"['chromosome xq26.3 duplication syndrome, X-linked dominant', 'chromosome Xq26 microduplication syndrome', 'chromosome Xq26.3 DUPLICATION syndrome', 'X-LAG (X-linked acrogigantism) due to dup(X)q(26)', 'familial infantile gigantism due to dup(X)q(26)', 'familial infantile gigantism due to Xq26 microduplication', 'X-linked acrogigantism']",,300942,448372,CN237731,,,,,,,,
mondo:0010492,"pituitary adenoma, growth hormone-secreting, 2","['pituitary adenoma 2, Growth hormone-secreting', 'PAGH2', 'pituitary adenoma, growth hormone-secreting, 2', 'pituitary adenoma 2, GH-secreting', 'PITA2', 'acromegaly, X-linked', 'GPR101 pituitary gland adenoma', 'pituitary adenoma, Growth hormone-secreting, type 2', 'pituitary gland adenoma caused by mutation in GPR101', 'acromegaly due to pituitary adenoma 2', 'pituitary adenoma 2, growth hormone-secreting']",0112007,300943,,C4012409,,,,,,,,
mondo:0010493,Diamond-Blackfan anemia 14 with mandibulofacial dysostosis,"['Diamond-Blackfan anemia 14 with mandibulofacial dysostosis', 'Diamond-Blackfan anemia caused by mutation in TSR2', 'Diamond-Blackfan anemia 14 with mandibulofacial dysostosis, X-linked recessive', 'Diamond-Blackfan anaemia caused by mutation in TSR2', 'DBA14', 'TSR2 Diamond-Blackfan anaemia', 'TSR2 Diamond-Blackfan anemia', 'Diamond-Blackfan anaemia 14 with mandibulofacial dysostosis, X-linked recessive']",0111897,300946,,C4225422,,,,,,,,
mondo:0010494,linear skin defects with multiple congenital anomalies 3,"['NDUFB11 microphthalmia with linear skin defects syndrome', 'LSDMCA3', 'linear skin defects with multiple congenital anomalies type 3', 'linear skin defects with multiple congenital anomalies 3, X-linked dominant', 'linear skin defects with multiple congenital anomalies 3', 'microphthalmia with linear skin defects syndrome caused by mutation in NDUFB11', 'linear skin defects with cardiomyopathy and Other congenital anomalies']",0111876,300952,,C4225421,,,,,,,,
mondo:0010495,"trichothiodystrophy 5, nonphotosensitive","['TTD5', 'trichothiodystrophy 5, nonphotosensitive', 'nonphotosensitive trichothiodystrophy caused by mutation in RNF113A', 'RNF113A nonphotosensitive trichothiodystrophy']",0111868,300953,,C4225420,,,,,,,,
mondo:0010496,X-linked intellectual disability-short stature-overweight syndrome,"['mental retardation, X-linked 12', 'intellectual disability, X-linked type 12', 'MRX12', 'intellectual disability, X-linked 12', 'intellectual developmental disorder, X-linked 12, X-linked recessive', 'mental retardation, X-linked 35', 'mental retardation, X-linked type 12', 'intellectual disability, X-linked 35']",0112056,300957,457240,C0796218,,,,,,,,
mondo:0010497,"intellectual disability, X-linked 102","['mental retardation, X-linked type 102', 'DDX3X non-syndromic X-linked intellectual disability', 'MRX102', 'intellectual disability, X-linked 102', 'intellectual developmental disorder, X-linked, syndrome, Snijders Blok type, X-linked recessive, X-linked dominant', 'intellectual disability, X-linked type 102', 'DDX3X-related intellectual disability', 'mental retardation, X-linked 102', 'non-syndromic X-linked intellectual disability caused by mutation in DDX3X']",,300958,,C4085582,,C129931,,,,,,
mondo:0010498,MEND syndrome,"['Male EBP disorder with neurologic defects', 'MEND', 'MEND syndrome, X-linked recessive', 'Male EBP disorder with neurological defects', 'MEND syndrome']",0111865,300960,401973,C4085243,"['-0.2423', '-0.0328', '0.413', '-0.4536', '0.1268', '-0.215', '-0.1532', '0.2455', '-0.4124', '-0.2051', '-0.2155', '-0.2351', '0.1427', '-0.2422', '-0.4023', '0.1158', '0.336', '-0.2278', '-0.1809', '-0.7046', '0.1489', '0.1536', '0.4272', '-0.04355', '0.04776', '0.0243', '-0.218', '0.07605', '0.4675', '-0.4302', '0.1505', '-0.0903', '0.4092', '0.07416', '0.1742', '-0.007866', '0.003569', '-0.1648', '-0.1464', '-0.3694', '0.2365', '-0.2239', '0.02802', '0.07355', '-0.05362', '-0.3965', '0.11163', '0.298', '-0.246', '-0.002743', '-0.4138', '0.09735', '-0.02382', '-0.01747', '-0.2722', '-0.1207', '0.1315', '-0.03065', '-0.392', '0.0915', '0.135', '0.06665', '-0.287', '0.2416', '-0.0259', '-0.0636', '0.1895', '0.3508', '-0.2328', '0.3945', '-0.54', '0.1377', '0.05457', '0.1991', '-0.3364', '-0.04807', '0.3428', '-0.382', '-0.2185', '-0.2493', '0.12476', '0.009315', '0.05417', '0.5874', '0.03625', '-0.07056', '-0.1294', '0.4907', '0.05078', '0.1749', '0.2401', '0.61', '0.4595', '0.1733', '0.5703', '0.05008', '0.3735', '-0.208', '0.58', '0.2573']",,,,,,,
mondo:0010499,Ritscher-Schinzel syndrome 2,"['RTSC2', 'CCDC22 Ritscher-Schinzel syndrome', 'Ritscher-Schinzel syndrome caused by mutation in CCDC22', 'Ritscher-Schinzel syndrome 2, X-linked recessive', 'Ritscher-Schinzel syndrome type 2', 'Ritscher-Schinzel syndrome 2']",0060572,300963,,C4225419,,,,,,,,
mondo:0010500,"intellectual disability, X-linked, syndromic 33","['MRXS33', 'TAF1 X-linked syndromic intellectual disability', 'intellectual disability, X-linked, syndromic 33', 'intellectual developmental disorder, X-linked syndromic 33, X-linked recessive', 'X-linked syndromic intellectual disability caused by mutation in TAF1', 'mental retardation, X-linked, syndromic 33', 'mental retardation, X-linked, syndromic type 33', 'intellectual disability, X-linked, syndromic type 33']",,300966,,C4225418,,,,,,,,
mondo:0010501,syndromic X-linked intellectual disability 34,"['syndromic X-linked intellectual disability Mircsof-Langouet type', 'mental retardation, X-linked, syndromic, Mircsof-Langouet type', 'intellectual developmental disorder, X-linked syndromic 34', 'X-linked syndromic intellectual disability caused by mutation in NONO', 'MRXSML', 'NONO X-linked syndromic intellectual disability', 'syndromic X-linked intellectual disability type 34', 'mental retardation, X-linked, syndromic 34', 'intellectual disability, X-linked, syndromic, Mircsof-Langouet type', 'macrocephaly-intellectual disability-left ventricular non compaction syndrome', 'syndromic X-linked mental retardation Mircsof-Langouet type', 'intellectual disability, X-linked, syndromic 34', 'mental retardation, X-linked, syndromic type 34', 'intellectual disability, X-linked, syndromic type 34', 'MRXS34']",0060817,300967,466791,,,,,,,,,
mondo:0010502,"intellectual disability, X-linked 99, syndromic, female-restricted","['USP9X X-linked syndromic intellectual disability', 'MRXS99F', 'intellectual developmental disorder, X-linked 99, syndromic, female-restricted, X-linked dominant', 'mental retardation, X-linked 99, syndromic, female-restricted', 'intellectual disability, X-linked 99, syndromic, female-restricted', 'X-linked syndromic intellectual disability caused by mutation in USP9X']",0112025,300968,,,,,,,,,,
mondo:0010503,Bartter disease type 5,"['MAGED2 Bartter syndrome', 'BARTS5', 'Bartter syndrome caused by mutation in MAGED2', 'Bartter syndrome, type 5, antenatal, transient', 'Bartter syndrome, type 5, antenatal, transient, X-linked recessive']",0110147,300971,570371,C4310820,,,,,,,,
mondo:0010504,immunodeficiency 47,"['immunodeficiency type 47', 'immunodeficiency 47, X-linked recessive', 'immunodeficiency 47', 'primary immunodeficiency disease caused by mutation in ATP6AP1', 'ATP6AP1 primary immunodeficiency disease', 'immunodeficiency and hepatopathy with or without neurologic features', 'IMD47']",0112002,300972,,C4310819,"['-0.00823', '0.0769', '-0.004547', '-0.02583', '0.0502', '-0.06165', '0.0316', '0.05756', '-0.03497', '-0.03308', '-0.02602', '0.002918', '-0.01897', '0.01551', '-0.0214', '-0.0624', '0.00957', '-0.0321', '-0.02759', '-0.11536', '-0.03946', '-0.01837', '0.07996', '-0.03033', '0.03833', '-0.01881', '-0.02171', '-0.01351', '-0.011406', '-0.04456', '0.0443', '0.01564', '0.0836', '0.004963', '0.02809', '-0.01982', '-0.03308', '-0.03552', '-0.04608', '-0.0644', '0.01894', '-0.0688', '0.0214', '-0.067', '-0.0227', '-0.055', '-0.0373', '0.0213', '0.02243', '0.01522', '-0.01253', '-0.0369', '0.02548', '0.01973', '-0.0532', '-0.01991', '0.04904', '-0.06964', '-0.0708', '0.001738', '0.0565', '0.02278', '0.00205', '0.01558', '0.0455', '-0.001687', '0.04727', '0.0409', '-0.0855', '0.0755', '-0.06186', '-0.003069', '0.00523', '-0.01883', '0.03436', '0.01533', '0.02274', '-0.009514', '-0.00921', '-0.0347', '0.00918', '0.007767', '-0.0306', '0.05264', '-0.01694', '-0.00227', '0.05026', '0.0702', '0.0932', '0.01212', '0.0461', '0.06647', '0.007236', '0.01049', '0.1492', '0.0639', '0.05664', '-0.10333', '-0.003336', '0.03198']",,,,,,,
mondo:0010505,intellectual disability-balding-patella luxation-acromicria syndrome,"['SHLTS', 'Scholte syndrome', 'early balding, patella luxation, acromicria and hypogonadism', 'early balding, patella luxation, acromicria, and hypogonadism', 'Scholte-Begeer-van Essen syndrome', 'SCHOLTE syndrome']",,300977,3041,C1866985,,,,C536638,,,,
mondo:0010506,"intellectual disability, X-linked 61","['mental retardation, X-linked type 61', 'intellectual disability, X-linked 61', 'intellectual disability, X-linked type 61', 'MRX61', 'RLIM non-syndromic X-linked intellectual disability', 'non-syndromic X-linked intellectual disability caused by mutation in RLIM', 'mental retardation, X-linked 61', 'Tonne-Kalscheuer syndrome']",0112042,300978,,C4283894,,,,,,,,
mondo:0010507,Xq25 microduplication syndrome,"['Xq25 duplication syndrome', 'Xq25 triplication syndrome']",,300979,521258,C4311049,,C177544,,,,,,
mondo:0010508,"intellectual disability, X-linked 103","['MRX103', 'mental retardation, X-linked type 103', 'non-syndromic X-linked intellectual disability caused by mutation in KLHL15', 'mental retardation, X-linked 103', 'intellectual disability, X-linked 103', 'KLHL15 non-syndromic X-linked intellectual disability', 'intellectual developmental disorder, X-linked 103, X-linked recessive', 'intellectual disability, X-linked type 103']",0112020,300982,,C4310818,,,,,,,,
mondo:0010509,"intellectual disability, X-linked 104","['mental retardation, X-linked type 104', 'non-syndromic X-linked intellectual disability caused by mutation in FRMPD4', 'MRX104', 'mental retardation, X-linked 104', 'intellectual disability, X-linked 104', 'FRMPD4 non-syndromic X-linked intellectual disability', 'intellectual disability, X-linked type 104', 'intellectual developmental disorder, X-linked 104']",0112018,300983,,C4310817,,,,,,,,
mondo:0010510,"intellectual disability, X-linked 105","['USP27X non-syndromic X-linked intellectual disability', 'intellectual disability, X-linked 105', 'MRX105', 'mental retardation, X-linked type 105', 'mental retardation, X-linked 105', 'intellectual developmental disorder, X-linked 105, X-linked recessive', 'non-syndromic X-linked intellectual disability caused by mutation in USP27X', 'intellectual disability, X-linked type 105']",0112036,300984,,C4310816,,,,,,,,
mondo:0010511,"vas deferens, congenital bilateral aplasia of, X-linked","['CBAVDX', 'congenital bilateral absence of vas deferens, X-linked', 'vas deferens, congenital bilateral aplasia of, X-linked']",0111863,300985,,C4310815,,,,,,,,
mondo:0010512,"intellectual disability, X-linked, syndromic, Bain type","['intellectual disability, X-linked, syndromic, Bain type', 'intellectual developmental disorder, X-linked, syndromic, Bain type, X-linked dominant', 'mental retardation, X-linked, syndromic, Bain type', 'MRXSB']",,300986,,C4310814,,,,,,,,
mondo:0010514,combined immunodeficiency due to moesin deficiency,"['X-linked Moesin-associated immunodeficiency', 'immunodeficiency 50', 'immunodeficiency type 50', 'IMD50', 'MSN-related combined immunodeficiency', 'CID due to Moesin deficiency', 'immunodeficiency 50, X-linked recessive']",0112001,300988,504530,C4310812,,,,,,,,
mondo:0010515,Meester-Loeys syndrome,"['Meester-Loeys syndrome', 'MRLS']",0111861,300989,,C4310811,,C187989,,,,,,
mondo:0010516,"midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis","['midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis', 'midface hypoplasia, hearing impairment, elliptocytosis, and nephrocalcinosis, X-linked recessive', 'MFHIEN']",0111859,300990,,C4310810,,,,,,,,
mondo:0010517,"ciliary dyskinesia, primary, 36, X-linked","['ciliary dyskinesia, primary, 36, X-linked', 'primary ciliary dyskinesia caused by mutation in PIH1D3', 'CILD36', 'ciliary dyskinesia, primary, 36, with or without situs inversus', 'PIH1D3 primary ciliary dyskinesia', 'ciliary dyskinesia, primary, 36, X-linked, X-linked recessive']",0111850,300991,,CN240511,,,,,,,,
mondo:0010518,Wiskott-Aldrich syndrome,"['Wiskott-Aldrich syndrome, X-linked recessive', 'Wiskott Aldrich syndrome', 'Wiskott-Aldrich syndrome 1', 'Wiskott syndrome', 'eczema-thrombocytopenia-immunodeficiency syndrome', 'WAS', 'immunodeficiency 2', 'Aldrich syndrome', 'eczema thrombocytopenia immunodeficiency syndrome', 'Imd 2', 'Wiskott-Aldrich syndrome']",9169,301000,906,C0043194,"['0.1542', '-0.3616', '-0.453', '-0.3691', '-0.05463', '-0.00347', '0.1609', '0.7583', '-0.07117', '-0.663', '0.3364', '0.3267', '0.11115', '0.1876', '0.2238', '-0.1799', '-0.344', '-0.05753', '0.248', '-0.8403', '0.03256', '-0.5176', '0.8286', '-0.3604', '0.1888', '-0.3855', '-0.435', '0.07214', '0.0844', '-0.6074', '0.5796', '0.1577', '0.618', '0.3123', '-0.1989', '-0.0175', '-0.314', '-0.7505', '-0.3994', '0.1176', '-0.3208', '0.01038', '0.528', '-0.7354', '-0.001704', '-0.03625', '-0.225', '-0.2303', '0.2168', '0.1268', '0.1987', '0.0387', '0.4348', '0.1533', '-0.442', '0.3337', '0.3494', '-0.7827', '-0.3909', '0.05536', '0.268', '0.8677', '-0.4517', '0.09656', '0.836', '0.1641', '0.425', '0.02872', '-0.1334', '0.7314', '-0.0781', '-0.786', '-0.7837', '-0.03308', '0.456', '-0.1832', '0.16', '-0.02959', '0.376', '0.1918', '-0.3599', '-0.4097', '-0.3816', '0.2253', '-0.635', '0.3577', '0.0909', '0.2002', '0.2391', '0.04117', '0.358', '0.147', '0.03053', '0.03024', '0.651', '0.2622', '-0.3093', '-0.5825', '-0.06573', '-0.7437']",C3448,,D014923,279.12,D82.0,10047992,
mondo:0010519,alpha thalassemia-X-linked intellectual disability syndrome,"['ALPHA-thalassemia/mental retardation syndrome, X-linked', 'Alpha thalassemia X-linked intellectual disability syndrome', 'Alpha-thalassemia-X-linked intellectual disability syndrome', 'ATR-X syndrome', 'alpha-thalassemia/intellectual disability syndrome nondeletion type', 'ATR, Nondeletion type', 'Alpha thalassemia X-linked mental retardation syndrome', 'XLMR hypotonic face syndrome', 'ATR, nondeletion type', 'Alpha thalassemia/intellectual disability syndrome X-linked', 'ATRX syndrome', 'alpha-thalassemia/mental retardation syndrome, X-linked dominant', 'Alpha thalassemia/mental retardation syndrome X-linked', 'Alpha-thalassemia/intellectual disability syndrome, Nondeletion type', 'ATRX', 'Alpha-thalassemia/mental retardation syndrome, Nondeletion type', 'alpha-thalassemia/mental retardation syndrome nondeletion type', 'Alpha thalassemia mental retardation syndrome, nondeletion type, X-linked', 'ALPHA-thalassemia/intellectual disability syndrome, X-linked', 'Alpha thalassemia intellectual disability syndrome, nondeletion type, X-linked', 'Alpha-thalassemia X-linked intellectual disability syndrome']",0110030,301040,847,C1845055,"['-0.2764', '0.534', '0.2795', '-0.628', '-0.1421', '-0.2747', '-0.662', '1.407', '-1.174', '-0.9595', '-0.2166', '-0.142', '0.218', '0.7046', '-0.3113', '0.02367', '-1.283', '-0.2325', '-0.6875', '-0.4504', '-0.4182', '0.02805', '0.691', '-0.3704', '0.819', '-0.585', '0.2922', '0.0508', '0.7563', '-0.731', '-0.07745', '-0.4004', '0.1594', '-0.457', '-0.5776', '-0.4814', '-0.7534', '-0.3647', '-0.453', '-0.7837', '0.5986', '0.301', '0.2372', '-0.2766', '-0.7915', '-0.712', '-0.654', '-0.6533', '0.1855', '-0.672', '-0.2421', '-0.5557', '0.004505', '0.3518', '-0.0938', '0.3054', '-0.369', '0.959', '0.02072', '0.493', '-0.4287', '-0.1351', '0.03845', '-0.2034', '-0.5845', '-0.006504', '0.1177', '0.759', '-0.9663', '0.6924', '-0.2029', '0.586', '-0.2343', '-0.05527', '0.1763', '0.0832', '-0.004364', '0.0396', '-0.333', '0.3313', '-0.2079', '-0.696', '0.01906', '-0.089', '-0.2017', '-0.0418', '-0.04068', '0.1533', '-0.01822', '0.7686', '0.2559', '0.3962', '-0.1746', '-0.0671', '0.73', '0.5107', '-0.689', '-0.3186', '0.2322', '-0.775']",C118631,,C538258,,D56.0,,
mondo:0010520,X-linked Alport syndrome,"['nephropathy and deafness, X-linked', 'Alport syndrome, X-linked', 'Alport syndrome 1, X-linked, X-linked dominant', 'congenital hereditary hematuria', 'ATS', 'hemorrhagic hereditary nephritis', 'hemorrhagic familial nephritis']",0110034,301050,88917,,"['0.04584', '0.0883', '-0.09644', '-0.10425', '0.02289', '-0.3955', '-0.03983', '0.09827', '-0.3474', '-0.12366', '0.127', '-0.2439', '-0.05887', '-0.0607', '-0.04242', '-0.1597', '-0.0864', '-0.002762', '0.0977', '-0.3774', '-0.0378', '0.069', '0.4578', '0.2751', '0.1296', '-0.1087', '-0.04422', '-0.1135', '0.1387', '0.00976', '0.1484', '0.1188', '0.3132', '-0.0005755', '0.045', '-0.1647', '-0.09436', '-0.00011307', '-0.0965', '-0.314', '-0.2805', '-0.3071', '0.09326', '0.09174', '-0.1761', '-0.2913', '-0.2368', '-0.1959', '0.4229', '-0.06323', '0.0936', '-0.276', '0.2216', '-0.3113', '0.07153', '-0.4592', '0.542', '0.11163', '-0.4338', '0.1586', '0.2083', '-0.1287', '0.2357', '0.2441', '0.0868', '-0.3044', '0.1842', '0.3762', '-0.3667', '0.3389', '-0.4097', '-0.2001', '0.2383', '0.174', '0.1969', '0.1503', '0.05246', '0.3518', '-0.1764', '0.2115', '-0.1135', '0.07245', '-0.0801', '0.2225', '-0.284', '-0.05368', '0.282', '0.2166', '0.01662', '0.0388', '0.1571', '0.0981', '0.093', '0.0661', '0.39', '0.3044', '0.3977', '-0.5854', '-0.0348', '0.12256']",,,,,,10001843,
mondo:0010521,amelogenesis imperfecta type 1E,"['X-linked amelogenesis imperfecta 1', 'amelogenesis imperfecta, X-linked 1', 'amelogenesis imperfecta, type 1E', 'X-linked enamel hypoplasia', 'amelogenesis imperfecta, hypomaturation type, with Snow-capped teeth', 'AMELX amelogenesis imperfecta', 'enamel hypoplasia X-linked', 'AIH1', 'amelogenesis imperfecta, type 1E, X-linked dominant', 'enamel hypoplasia, X-linked', 'amelogenesis imperfecta hypoplastic/hypomaturation X-linked 1', 'amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 1', 'X-linked amelogenesis imperfecta hypoplastic/hypomaturation 1', 'amelogenesis imperfecta caused by mutation in AMELX', 'amelogenesis imperfecta X-linked 1', 'amelogenesis imperfecta hypomaturationtype with snow-capped teeth', 'amelogenesis imperfecta, type IE', 'AI1E', 'amelogenesis imperfecta type IE']",0110058,301200,,,,,,,,,,
mondo:0010522,X-linked amelogenesis imperfecta hypoplastic/hypomaturation 2,"['amelogenesis imperfecta 3, hypoplastic type', 'amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked 2', 'amelogenesis imperfecta, hypoplastic/hypomaturation, X-linked type 2', 'X-linked amelogenesis imperfecta hypoplastic/hypomaturation type 2', 'amelogenesis imperfecta 3, hypoplastic type (formerly)', 'amelogenesis imperfecta type IE X-linked 2', 'amelogenesis imperfecta, type IE, X-linked 2', 'amelogenesis imperfecta 3, hypoplastic type, formerly', 'X-linked enamel hypoplasia', 'enamel hypoplasia, X-linked', 'AIH3 (formerly)', 'AIH3', 'amelogenesis imperfecta 3 hypoplastic type']",0110059,301201,,C1845051,,,,,,,,
mondo:0010523,X-linked reticulate pigmentary disorder,"['pigmentary disorder, reticulate, with systemic manifestations, X-linked', 'amyloidosis, familial cutaneous', 'Partington disease', 'PDR', 'XLPDR', 'pigmentary disorder, reticulate, with systemic manifestations, X-linked, X-linked recessive', 'X-linked cutaneous amyloidosis', 'familial cutaneous amyloidosis', 'pigmentary disorder, reticulate, with systemic manifestations']",0111834,301220,85453,,"['0.386', '-0.02997', '-0.915', '-0.4243', '0.3723', '-0.413', '-0.3647', '0.3123', '-0.575', '-0.1716', '-0.3699', '0.05795', '-0.8057', '0.2161', '-0.3755', '0.3945', '0.2812', '-0.0461', '-0.249', '-0.527', '-0.00475', '-0.1837', '0.542', '-0.3528', '0.0917', '0.2365', '-0.1952', '0.04953', '-0.1829', '-0.32', '0.5767', '-0.3374', '0.0451', '-0.2827', '0.2231', '-0.008255', '-0.03473', '-0.2047', '-0.186', '-0.1656', '0.251', '-0.3474', '0.1829', '-0.5327', '0.397', '-0.2184', '-0.1731', '-0.096', '-0.3577', '0.2346', '0.1788', '0.267', '0.5176', '-0.12256', '-0.2296', '-0.3125', '0.7715', '-0.13', '-0.1738', '-0.3555', '0.3953', '-0.01987', '0.1907', '0.1194', '0.7227', '-0.0567', '0.7197', '1.123', '0.00766', '0.2554', '-0.609', '-0.2272', '-0.09155', '0.739', '-0.05637', '-0.1597', '-0.2954', '0.323', '-0.001009', '-0.2644', '0.0716', '-0.2695', '-0.3555', '0.2957', '0.3801', '-0.23', '0.251', '0.1809', '0.3857', '-0.0785', '0.206', '0.445', '0.3345', '0.2319', '0.4988', '0.01627', '-0.1897', '-0.2737', '0.3618', '-0.0873']",,,C564461,,,,
mondo:0010524,X-linked sideroblastic anemia with ataxia,"['anemia sideroblastic and spinocerebellar ataxia', 'anemia, sideroblastic, with ataxia, X-linked recessive', 'anaemia sideroblastic and spinocerebellar ataxia', 'X-linked sideroblastic anemia and spinocerebellar ataxia', 'X-linked sideroblastic anaemia and ataxia', 'X-linked sideroblastic anemia and ataxia', 'sideroblastic anemia with spinocerebellar ataxia', 'X-linked sideroblastic anaemia and spinocerebellar ataxia', 'ASAT', 'sideroblastic anaemia with spinocerebellar ataxia', 'anemia, Sex-linked hypochromic Siderobla', 'Pagon Bird Detter syndrome', 'X-linked sideroblastic Anemia and ataxia', 'X-linked sideroblastic anemia with ataxia', 'X-linked sideroblastic anaemia with spinocerebellar ataxia', 'X-linked sideroblastic Anaemia and ataxia', 'Xlsa-A', 'XLSA-A', 'anemia, sideroblastic, and spinocerebellar ataxia', 'Pagon-Bird-Detter syndrome']",0060064,301310,2802,C4304338,"['-0.3147', '0.3933', '-0.2178', '0.4062', '0.1674', '0.02737', '-0.0956', '0.639', '-0.3315', '-0.3455', '0.4875', '0.00452', '0.2783', '0.3486', '-0.5537', '-0.09644', '-0.6313', '0.1287', '-0.537', '-0.484', '-0.02615', '-0.4602', '-0.2223', '-0.1964', '0.67', '-0.5176', '-0.08624', '-0.4497', '0.221', '0.3638', '-0.228', '0.05582', '0.4614', '0.4443', '0.2683', '-0.5093', '-0.5254', '-0.5835', '0.2822', '-0.2239', '-0.66', '0.2766', '-0.1343', '-0.1716', '-0.744', '-0.778', '-0.10815', '0.4612', '0.4338', '-0.5405', '0.2313', '0.554', '0.572', '-0.1826', '0.54', '-0.5566', '0.078', '-0.01073', '-1.189', '0.006287', '0.2336', '0.2404', '-0.106', '-0.1224', '0.1316', '0.2812', '0.1681', '0.951', '-0.4348', '0.807', '1.02', '-0.355', '-0.912', '-0.7915', '0.506', '0.8213', '0.05878', '-0.251', '-0.05157', '-0.04883', '0.1624', '-0.351', '0.2947', '0.2937', '0.4797', '-0.2856', '-0.865', '-0.0223', '0.679', '-0.00411', '0.551', '0.2499', '-0.3933', '-0.05374', '0.314', '0.86', '0.1884', '0.2225', '0.4072', '-0.4727']",,,C536358,,,,
mondo:0010525,"neural tube defects, X-linked","['anencephaly and spina bifida X-linked', 'spina bifida, X-linked', 'X-linked anencephaly/spina bifida', 'neural tube defects, X-linked']",,301410,,C1845026,,,,C536359,,,,
mondo:0010526,Fabry disease,"['Anderson-Fabry disease', 'Alpha-galactosidase A deficiency', 'Fabry disease, Cardiac variant', 'ceramide trihexosidase deficiency', 'Fabry^s disease', 'angiokeratoma corporis diffusum', 'Gla deficiency', 'hereditary dystopic lipidosis', 'angiokeratoma, diffuse', 'deficiency of melibiase', 'Fabry disease', 'diffuse angiokeratoma', 'Fd', 'alpha galactosidase deficiency']",14499,301500,324,C0002986,"['-0.4604', '-0.1067', '-0.503', '-0.2089', '-0.03494', '-0.551', '0.3103', '0.741', '0.2708', '0.1879', '-0.3296', '-0.2368', '0.10583', '0.2054', '-0.638', '0.1616', '-0.386', '-0.2632', '-0.2434', '-0.2686', '-0.06207', '-0.3992', '0.407', '-0.0704', '-0.4482', '-0.587', '0.2742', '0.3074', '0.269', '-0.2783', '0.843', '0.1757', '0.5273', '0.0903', '0.1536', '-0.925', '-0.1171', '0.01897', '0.2927', '-0.03778', '0.3179', '-0.6196', '0.699', '0.1641', '0.336', '0.3691', '-0.643', '-0.2395', '0.1453', '0.3115', '0.259', '1.047', '0.3582', '0.04794', '0.4246', '-0.332', '0.7007', '-0.8047', '-0.5547', '-0.1743', '-0.08203', '-0.09796', '0.003654', '-0.063', '0.1554', '0.2094', '0.637', '0.1769', '0.1595', '0.1042', '-0.3896', '-0.5366', '-0.004284', '0.512', '0.6978', '0.7354', '0.5312', '0.01598', '0.1283', '-0.2969', '0.2979', '-0.1583', '-0.2468', '-0.11127', '0.07404', '0.4705', '0.2084', '0.2274', '-0.03033', '0.23', '0.3018', '-0.4822', '-0.3936', '-0.2158', '0.758', '0.09894', '0.1884', '-0.0915', '-0.1236', '0.741']",C84701,,D000795,,,10016016,
mondo:0010528,anosmia,"['anosmia', 'anosmia (disease)']",,,,C0003126,,,,D000857,,,,0000458
mondo:0010529,X-linked spinocerebellar ataxia type 3,"['spinocerebellar ataxia X-linked type 3', 'ataxia-deafness syndrome, X-linked', 'spinocerebellar ataxia, X-linked 3', 'ataxia-deafness syndrome X-linked', 'X-linked ataxia-deafness syndrome', 'SCAX3', 'spinocerebellar ataxia, X-linked type 3', 'Scax3']",0111831,301790,85297,C1844936,,,,C537315,,,,
mondo:0010531,contractures-ectodermal dysplasia-cleft lip/palate syndrome,"['contractures ectodermal dysplasia cleft lip palate', 'congenital contractures, ectodermal dysplasia, cleft lip/palate, and developmental impairment', 'Ladda-Zonana-Ramer syndrome', 'arthrogryposis, ectodermal dysplasia, cleft LIP/palate, and developmental delay', 'Ladda Zonana Ramer syndrome']",,301815,1484,,,,,,,,,
mondo:0010532,infantile-onset X-linked spinal muscular atrophy,"['arthrogryposis multiplex congenita, distal, X-linked', 'arthrogryposis, X-linked, type 1', 'spinal muscular atrophy, X-linked 2, infantile, X-linked recessive', 'spinal muscular atrophy, X-linked lethal infantile', 'spinal muscular atrophy with arthrogryposis', 'AMC, distal, X-linked', 'spinal muscular atrophy, infantile X-linked', 'X-linked distal arthrogryposis multiplex congenita', 'SMAX2', 'spinal muscular atrophy, X-linked type 2', 'spinal muscular atrophy, X-linked 2', 'X-linked spinal muscular atrophy type 2']",0111827,301830,1145,C1844934,"['-0.654', '0.0313', '0.09625', '-0.0727', '-0.406', '-0.956', '0.09595', '1.072', '-1.018', '-0.4607', '-0.01805', '0.1913', '-0.164', '0.07526', '-0.4138', '-0.1603', '-0.2808', '0.02356', '-0.1335', '-0.922', '-0.1373', '-0.206', '0.1742', '-0.3074', '0.07166', '-0.2864', '-0.502', '-0.0824', '-0.2612', '0.2283', '-0.134', '0.4727', '0.521', '0.701', '-0.1442', '-0.346', '-0.11847', '-0.11255', '0.2231', '0.01897', '-0.1823', '-0.142', '-0.3892', '0.3298', '-0.4006', '0.1323', '-0.2219', '0.1744', '0.2144', '-0.001394', '-0.672', '-0.2015', '0.1401', '-0.10394', '-0.007305', '-0.4402', '-0.1923', '0.2301', '0.3574', '0.209', '0.3018', '-0.08624', '-0.566', '-0.0787', '-0.3806', '-0.687', '1.056', '0.7925', '-0.0534', '0.0925', '0.3967', '0.2393', '0.6636', '-0.2219', '0.0681', '0.2347', '0.3174', '0.3113', '-0.6333', '-0.05066', '0.041', '0.2369', '0.3425', '0.1311', '-0.483', '0.793', '0.5176', '0.266', '0.4717', '-0.2166', '0.499', '0.5806', '0.954', '0.572', '0.3337', '0.2246', '0.8735', '0.03772', '0.08655', '0.11316']",,,C535380,,,,
mondo:0010533,Arts syndrome,"['MRXS18', 'lethal ataxia-deafness-optic atrophy', 'intellectual disability, X-linked, syndromic 18', 'Arts syndrome', 'mental retardation, X-linked, syndromic 18', 'ataxia, fatal X-linked, with deafness and loss of vision', 'Arts', 'Arts syndrome, X-linked recessive', 'lethal ataxia with deafness and optic atrophy', 'MRXSARTS', 'fatal X-linked ataxia with deafness and loss of vision', 'syndromic X-linked intellectual disability 18', 'syndromic X-linked intellectual disability Arts type', 'syndromic X-linked mental retardation 18', 'intellectual disability, X-linked, syndromic, Arts type', 'mental retardation, X-linked, syndromic, Arts type', 'X-linked fatal ataxia with deafness and loss of vision', 'syndromic X-linked mental retardation Arts type']",0050647,301835,1187,C0796028,"['-0.2246', '-0.001571', '-0.52', '-0.036', '-0.2122', '-0.751', '0.2737', '0.559', '-0.2461', '-0.1803', '-0.178', '-0.2001', '-0.4304', '-0.2593', '0.3545', '-0.2712', '0.2008', '0.215', '-0.161', '-0.628', '0.3442', '-0.1279', '-0.11237', '-0.415', '-0.3865', '0.083', '-0.3823', '0.1592', '-0.1511', '-0.629', '0.252', '0.1881', '0.1471', '-0.1735', '-0.397', '-0.2223', '-0.118', '-0.504', '-0.2988', '-0.1005', '0.06097', '-0.1427', '0.34', '-0.0769', '-0.0016575', '-0.3699', '-0.12146', '-0.11786', '-0.9443', '0.08826', '-0.3413', '0.2673', '0.11176', '-0.1206', '0.564', '-0.4233', '0.776', '-0.0844', '-0.1544', '0.551', '-0.1752', '-0.2179', '0.2109', '0.4963', '-0.3682', '-0.04123', '0.1909', '0.504', '-0.6963', '0.9175', '-0.3765', '0.0926', '-0.04623', '-0.4207', '0.395', '-0.525', '-0.1975', '0.1688', '-0.1345', '0.2317', '0.1448', '0.4722', '0.235', '0.9463', '0.1537', '0.0478', '-0.2688', '0.4104', '0.2627', '0.002708', '0.3652', '0.6743', '0.2499', '-0.056', '0.5093', '0.2554', '0.5034', '-0.006847', '0.334', '-0.1875']",,,C535388,277.2,,,
mondo:0010534,X-linked spinocerebellar ataxia type 4,"['spinocerebellar ataxia X-linked type 4', 'SCAX4', 'spinocerebellar ataxia, X-linked type 4', 'ataxia-dementia syndrome X-linked', 'ataxia-dementia syndrome, X-linked', 'spinocerebellar ataxia, X-linked 4', 'Scax4', 'X-linked ataxia-dementia syndrome']",0111832,301840,85292,C1844933,,,,C537316,,,,
mondo:0010535,Bazex-Dupre-Christol syndrome,"['Bazex-Dupre-Christol syndrome', 'Bazex-Dupré-Christol syndrome', 'BDCS', 'acrokeratosis of Bazex', 'acrokeratosis paraneoplastica of Bazex', 'follicular atrophoderma and basal cell carcinomas', 'follicular atrophoderma-basal cell carcinoma syndrome', 'BZX', 'Bazex syndrome', 'follicular atrophoderma-basocellular proliferations-hypotrichosis syndrome', 'acrokeratosis paraneoplastica', 'Bazex syndrome, X-linked dominant']",,301845,166113,CN200039,,,,,757.39,,,
mondo:0010536,"tubulin, beta","['tubulin, beta']",,301850,,,,,,,,,,
mondo:0010537,Borjeson-Forssman-Lehmann syndrome,"['syndromic X-linked intellectual disability Borjeson-Forssman-Lehmann type', 'BFLS', 'BORJ', 'intellectual disability, epilepsy, and endocrine disorder', 'intellectual disability-epilepsy-endocrine disorders syndrome', 'syndromic X-linked mental retardation Borjeson-Forssman-Lehmann type', 'MRXSBFL', 'mental retardation, X-linked, syndromic, Borjeson-Forssman-Lehmann type', 'mental retardation, epilepsy, and endocrine disorders', 'mental deficiency, epilepsy and endocrine disorders', 'Borjeson-Forssman-Lehmann syndrome, X-linked recessive', 'mental retardation, epilepsy, and endocrine disorder', 'Borjeson-FORSSMAN-Lehmann syndrome', 'intellectual disability, X-linked, syndromic, Borjeson-Forssman-Lehmann type', 'intellectual deficiency-epilepsy-endocrine disorders syndrome', 'Borjeson-Forssman-Lehmann syndrome', 'intellectual disability, epilepsy, and endocrine disorders', 'Borjeson syndrome']",0050681,301900,127,C0265339,"['0.1556', '0.2135', '-0.08624', '0.1744', '-0.2451', '-0.844', '0.5728', '0.9053', '-0.5825', '-0.3892', '0.2837', '-0.1803', '0.1511', '0.348', '-0.3494', '0.07043', '0.5483', '-0.1938', '-0.174', '-0.4382', '0.0891', '-0.2072', '0.6426', '-0.1213', '-0.295', '-0.02261', '-0.7764', '-0.2439', '0.329', '-0.5312', '0.5273', '-0.2227', '0.6714', '0.1208', '0.3906', '-0.2786', '-0.2915', '-0.2338', '-0.3323', '0.1263', '0.761', '-0.3745', '0.01334', '0.01834', '0.1467', '-0.3018', '0.10474', '0.2805', '-0.2338', '-0.03305', '-0.1008', '0.303', '0.09735', '0.1042', '0.016', '-0.0988', '0.3691', '-0.742', '0.2104', '0.2551', '-0.3254', '-0.1931', '-0.1396', '0.2844', '-0.3115', '0.6465', '-0.03314', '0.5063', '0.426', '0.308', '-0.0673', '0.2372', '-0.09814', '0.266', '0.423', '-0.0269', '-0.004875', '-0.726', '-0.2101', '-0.163', '0.2145', '-0.3066', '-0.6035', '0.0529', '-0.02255', '0.592', '-0.4836', '-0.5796', '0.3086', '0.638', '-0.182', '0.3008', '0.00981', '-0.095', '0.31', '0.04523', '-0.1375', '-0.547', '0.7124', '0.1615']",,,C536575,759.89,,,
mondo:0010538,Mononen-Karnes-Senac syndrome,"['short and abducted thumbs and great toes', 'thumbs and great toes, short and abducted', 'skeletal dysplasia-brachydactyly syndrome', 'Mononen type brachydactyly', 'thumbs and great toes short and abducted', 'Mononen Karnes Senac syndrome', 'skeletal dysplasia brachydactyly', 'brachydactyly, Mononen type', 'brachydactyly Mononen type']",0110973,301940,2565,C2931060,,,,C535914,,,,
mondo:0010539,X-linked mandibulofacial dysostosis,"['branchial arch syndrome, X-linked', 'mandibulofacial dysostosis, X-linked', 'branchial arch syndrome X-linked', 'X-linked mandibulofacial dysostosis with limb anomalies', 'mandibulofacial dysostosis, Toriello type', 'MFD Toriello type', 'X-linked branchial arch syndrome', 'mandibulofacial dysostosis Toriello type']",,301950,1131,C1844918,,,,C537102,,,,
mondo:0010540,"bullous dystrophy, macular type","['bullous dystrophy, hereditary macular type', 'EBM', 'epidermolysis bullosa macular type', 'epidermolysis bullosa, macular type', 'bullous dystrophy hereditary macular type']",,302000,1867,C0795974,,,,C563065,,,,
mondo:0010541,X-linked calvarial hyperostosis,"['isolated hyperostosis of the calvarium', 'calvarial hyperostosis']",,302030,391327,,,,,C537963,,,,
mondo:0010542,dilated cardiomyopathy 3B,"['DMD-related dilated cardiomyopathy', 'DMD dilated cardiomyopathy', 'X-linked dilated cardiomyopathy', 'cardiomyopathy, dilated, type 3B', 'cardiomyopathy, dilated, X-linked', 'CMD3B', 'dilated cardiomyopathy type 3B', 'dilated cardiomyopathy caused by mutation in DMD', 'cardiomyopathy, dilated, 3B']",0110461,302045,,C3668940,"['-0.0273', '0.03183', '-0.0001028', '-0.001352', '0.000688', '-0.04514', '0.003626', '0.0498', '-0.03406', '-0.001469', '-0.001339', '-0.01833', '0.0011835', '-0.010025', '-0.01671', '-0.01917', '-0.02124', '-0.01324', '-0.02191', '-0.05634', '-0.003548', '-0.013176', '0.02281', '-0.0083', '0.02179', '-0.00756', '0.006348', '-0.001592', '0.0002768', '-0.014435', '0.02101', '0.004913', '0.04172', '0.014404', '-0.01326', '-0.01654', '0.002691', '-0.0004497', '-0.010735', '-0.01534', '0.01843', '-0.03775', '0.02492', '-0.004883', '-0.01148', '-0.03032', '0.002853', '0.038', '0.006824', '0.000719', '-0.01591', '-0.005093', '0.003668', '0.01465', '-0.01203', '-0.01753', '0.0375', '-0.01043', '-0.03943', '0.00444', '0.01836', '0.0006876', '0.013145', '0.00854', '-0.02881', '-0.01216', '0.04584', '0.0405', '-0.0377', '0.02895', '-0.0367', '0.00208', '0.01593', '-0.01793', '0.02', '0.01833', '0.00808', '-0.0137', '-0.02208', '-0.01608', '0.010925', '-0.00893', '3.403e-05', '0.00747', '0.0081', '-0.01074', '0.01184', '0.02715', '0.04578', '0.001966', '0.02171', '0.0215', '0.001158', '0.01019', '0.0768', '0.01904', '0.02371', '-0.0322', '-0.007767', '0.0023']",,,C580047,425.4,,,
mondo:0010543,Barth syndrome,"['3-Methylglutaconicaciduria type II', 'MGA type II', 'Barth syndrome, X-linked recessive', 'X-linked cardioskeletal myopathy and neutropenia', '3-Methylglutaconicaciduria type 2', 'Barth syndrome', 'cardioskeletal myopathy-neutropenia syndrome', '3-Methylglutaconic aciduria, type 2', 'TAZ defect', '3-methylglutaconic aciduria type II', 'MGA2', 'BTHS', 'BARTH syndrome', '3-methylglutaconic aciduria type 2', 'Mga, type 2', 'cardioskeletal myopathy with neutropenia and abnormal mitochondria', 'MGA type 2']",0050476,302060,111,C0574083,"['-0.3733', '-0.2568', '0.006878', '-0.37', '0.4539', '-0.296', '0.175', '1.015', '-0.1444', '0.04926', '0.2217', '0.2479', '0.5845', '-0.3413', '-0.3037', '-0.2927', '-0.2358', '-0.1509', '-0.7227', '-0.571', '-0.2303', '-0.01208', '0.2291', '-0.3325', '-0.4485', '-0.4875', '-0.1697', '0.4866', '0.108', '-0.3604', '0.4263', '0.04147', '0.07306', '0.3289', '-0.6797', '0.2556', '-0.0431', '-0.10876', '-0.4858', '-0.3306', '-0.2034', '0.614', '-0.1638', '0.3484', '-0.811', '0.4548', '-0.0631', '0.4487', '0.02585', '0.399', '-0.3596', '-0.0952', '0.04074', '-0.02316', '0.219', '0.0741', '0.1725', '0.09875', '-0.3716', '0.03867', '0.0553', '0.4402', '0.415', '-0.0237', '0.05353', '0.0708', '0.7007', '0.6465', '-0.2085', '0.647', '-0.638', '-0.2349', '0.0666', '0.4268', '-0.03452', '-0.291', '0.02591', '-0.7896', '0.2043', '0.2292', '0.1877', '-0.3137', '-0.3992', '-0.2637', '0.196', '0.739', '0.1327', '-0.2861', '0.6265', '0.1578', '0.1803', '0.3296', '0.3237', '0.3804', '0.291', '0.906', '0.7544', '-0.379', '-0.1323', '-0.1758']",C84585,,D056889,,E78.71,,
mondo:0010544,cataract 40,"['NHS early-onset non-syndromic cataract', 'cataract 40 with or without microcornea', 'cataract, congenital, X-linked', 'cataract 40, X-linked', 'early-onset non-syndromic cataract caused by mutation in NHS', 'cataract type 40', 'cataract, congenital total, with posterior sutural opacities in heterozygotes', 'cataract 40', 'cataract, congenital, with microcornea or slight microphthalmia', 'CTRCT40', 'cataract congenital X-linked', 'cataract 40 X-linked']",0110272,302200,98994,,,,,C535338,,,,
mondo:0010545,Nance-Horan syndrome,"['cataract-dental syndrome', 'Nance-Horan syndrome', 'Mesiodens cataract syndrome', 'cataract X-linked with Hutchinsonian teeth', 'NHS', 'cataract dental syndrome', 'Mesiodens-cataract syndrome', 'nance-horan syndrome, X-linked dominant', 'cataract, X-linked, with Hutchinsonian teeth']",0060599,302350,627,C0796085,"['0.2524', '-0.204', '-0.3494', '-0.0946', '0.162', '0.1307', '0.01976', '0.988', '-0.7837', '-0.2087', '-0.478', '-0.4973', '0.3228', '0.4634', '-0.475', '-0.011765', '0.6113', '-0.2104', '-0.192', '-0.514', '-0.3694', '0.269', '0.494', '-0.138', '0.1442', '-0.1815', '-0.9575', '-0.0695', '0.786', '0.3748', '0.3025', '-0.1503', '-0.273', '0.3628', '0.07184', '0.10297', '0.2125', '-0.673', '-0.08', '-0.1855', '1.011', '-0.251', '0.4612', '-0.3435', '0.3628', '0.2593', '-0.07043', '0.03726', '-0.02217', '0.1276', '-0.1017', '0.3447', '-0.4065', '-0.3667', '-0.1321', '0.0753', '0.57', '-0.545', '-0.2556', '0.1181', '0.3884', '-0.337', '0.03156', '0.2474', '-0.0466', '-0.04102', '-0.2063', '0.2446', '0.07654', '0.3882', '-0.268', '0.2659', '-0.07196', '-0.2659', '0.2023', '-0.08923', '0.2292', '-0.5684', '-0.0763', '-0.08527', '0.1965', '-0.24', '-0.10645', '0.746', '-0.2129', '0.0898', '-0.3435', '0.311', '0.2944', '0.4136', '-0.2954', '0.9023', '0.00011194', '-0.154', '0.816', '-0.09375', '0.1298', '-0.9365', '0.1306', '0.06647']",,,C538336,759.89,,,
mondo:0010546,"central incisors, absence of","['central incisors, absence of']",,302400,,,,,,,,,,
mondo:0010547,X-linked progressive cerebellar ataxia,"['spinocerebellar ataxia, X-linked type 1', 'spinocerebellar ataxia, X-linked 1, X-linked recessive', 'OPCA, X-linked', 'SCAX1', 'spinocerebellar ataxia, X-linked 1', 'olivopontocerebellar atrophy, X-linked']",0111829,302500,1175,C0796205,"['-0.11707', '-0.2944', '-0.0508', '0.159', '-0.254', '-0.892', '0.0611', '0.02835', '-0.778', '-0.989', '0.1359', '0.3184', '-0.2761', '0.11237', '0.348', '-0.3647', '-0.1864', '-0.0854', '0.0665', '-0.943', '0.03726', '-0.2952', '0.09686', '-0.547', '0.641', '-0.548', '-0.3064', '0.1863', '-0.03096', '-0.866', '-0.004265', '0.4814', '-0.607', '-0.1686', '0.338', '0.0843', '-0.08496', '0.1514', '0.4688', '0.1769', '0.3367', '0.2903', '-0.4866', '0.3687', '0.509', '-0.719', '0.10126', '0.3962', '0.4739', '-0.1418', '-0.2861', '0.2341', '-0.2023', '-0.2993', '0.0795', '-0.765', '0.4575', '0.5156', '0.001242', '0.4763', '-0.4297', '0.303', '0.299', '-0.0766', '-0.524', '0.6235', '0.303', '0.5767', '-0.559', '0.3687', '0.776', '0.5093', '0.003517', '-0.7188', '0.721', '0.2278', '0.2815', '0.35', '0.1617', '0.4382', '-0.3633', '-0.825', '0.1735', '0.79', '-0.305', '-0.5845', '0.2153', '-0.01536', '0.441', '0.4082', '0.3613', '0.5312', '0.175', '0.2114', '0.9243', '1.031', '0.351', '0.3992', '-0.33', '0.04266']",,,C563134,,,,
mondo:0010548,"spinocerebellar ataxia, X-linked 2","['cerebellar ataxia with extrapyramidal involvement early-onset', 'Scax2', 'spinocerebellar ataxia X-linked type 2', 'spinocerebellar ataxia, X-linked type 2', 'cerebellar ataxia with extrapyramidal involvement, early-onset', 'spinocerebellar ataxia, X-linked 2']",0111830,302600,,C1844885,,,,C537314,,,,
mondo:0010549,Charcot-Marie-Tooth disease X-linked dominant 1,"['hereditary motor and sensory neuropathy, X-linked', 'X-linked Charcot-Marie-Tooth disease type 1', 'Charcot Marie Tooth disease X-linked 1', 'Charcot-Marie-Tooth disease type X caused by mutation in GJB1', 'Charcot-Marie-Tooth disease, X-linked dominant, 1', 'Charcot-Marie-Tooth disease, X-linked dominant, type 1', 'CMTX 1', 'CMT2, formerly', 'CMTX', 'CMT2', 'HMSN, X-linked', 'Charcot-Marie-Tooth neuropathy, X-linked dominant, 1, X-linked dominant', 'Charcot-Marie-Tooth neuropathy, X-linked, 1', 'Charcot-Marie-Tooth neuropathy X type 1', 'Charcot-Marie-Tooth disease X-linked dominant type 1', 'Charcot-Marie-Tooth peroneal muscular atrophy, X-linked', 'GJB1 Charcot-Marie-Tooth disease type X', 'CMTX1', 'Charcot-Marie-Tooth neuropathy X-linked dominant 1', 'CMT1X', 'Charcot-Marie-Tooth disease, X-linked, 1']",0110209,302800,101075,C0393808,"['0.02562', '0.2524', '0.283', '-0.08734', '-0.1321', '-0.1199', '-0.4949', '0.4487', '-0.78', '-0.4624', '0.0897', '0.2089', '-0.02599', '0.01747', '0.00404', '-0.248', '-0.3037', '-0.2712', '-0.437', '-0.321', '0.2008', '0.1707', '0.4993', '0.6455', '0.00169', '0.2798', '0.1578', '0.11945', '0.1731', '0.1783', '0.2123', '-0.4214', '0.2474', '0.113', '0.1827', '-0.8364', '-0.571', '-0.279', '0.2336', '-0.1715', '-1.121', '-0.617', '-0.4653', '0.5986', '-0.0716', '-0.1956', '0.0253', '0.1405', '-0.01747', '-0.0206', '-0.02745', '0.171', '-0.2285', '-1.2295', '0.1184', '-0.0545', '0.279', '0.1578', '-0.6226', '0.12354', '-0.3562', '0.1489', '0.771', '0.924', '-0.4666', '1.056', '-0.3096', '0.966', '-0.727', '0.3804', '-0.9937', '0.1246', '0.2715', '-0.0798', '1.014', '0.5703', '-0.1014', '0.5796', '0.452', '-0.0456', '-0.1115', '0.1738', '1.001', '0.479', '-0.03745', '0.07245', '-0.03644', '0.565', '0.652', '0.2266', '0.0955', '-0.1805', '0.1547', '0.151', '0.5947', '0.3745', '0.537', '-0.8257', '-0.02206', '0.2324']",C129068,,,,,,
mondo:0010550,Charcot-Marie-Tooth disease X-linked recessive 2,"['Charcot-Marie-Tooth neuropathy, X-linked recessive, 2, X-linked recessive', 'Charcot Marie Tooth disease X-linked recessive 2', 'Charcot-Marie-Tooth neuropathy X-linked recessive 2', 'X-linked Charcot-Marie-Tooth disease type 2', 'Charcot-Marie-Tooth disease X-linked recessive type 2', 'Charcot-Marie-Tooth neuropathy, X-linked recessive, 2', 'CMTX 2', 'CMTX2', 'Charcot-Marie-Tooth disease, X-linked recessive, 2']",0110208,302801,101076,C1844873,,,,C535302,,,,
mondo:0010551,Charcot-Marie-Tooth disease X-linked recessive 3,"['Charcot-Marie-Tooth neuropathy, X-linked recessive, 3, X-linked recessive', 'Charcot-Marie-Tooth neuropathy, X-linked recessive, 3', 'Charcot-Marie-Tooth disease, X-linked recessive, 3', 'Charcot-Marie-Tooth neuropathy X-linked recessive 3', 'CMTX3', 'CMT3X', 'Charcot Marie Tooth disease X-linked recessive 3', 'X-linked Charcot-Marie-Tooth disease type 3', 'Charcot-Marie-Tooth disease X-linked recessive type 3', 'CMTX 3']",0110211,302802,101077,C1844865,,,,C535303,,,,
mondo:0010552,"Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita","['Charcot-Marie-Tooth peroneal muscular atrophy, X-linked, with aplasia cutis congenita']",,302803,,C1844864,,,,C538077,,,,
mondo:0010553,"Charcot-Marie-Tooth peroneal muscular atrophy and Friedreich ataxia, combined","['Charcot-Marie-Tooth peroneal muscular atrophy and Friedreich ataxia, combined']",,302900,,C1844863,,,,C564446,,,,
mondo:0010554,Abruzzo-Erickson syndrome,"['cleft palate-coloboma-deafness syndrome', 'CHARGE-like syndrome', 'CHARGE-like syndrome, X-linked', 'ABERS', 'CHARGE like syndrome X-linked', 'Abruzzo-Erickson syndrome']",0111826,302905,921,C1844862,"['-0.1417', '0.2712', '-0.03625', '-0.307', '0.3757', '-0.6323', '0.2045', '0.7944', '0.2339', '-0.9614', '0.626', '-0.5728', '0.2346', '0.2627', '0.006847', '-0.4292', '0.00587', '-0.4988', '-0.523', '-0.354', '-0.302', '-0.1992', '0.05008', '-0.3367', '0.669', '0.1167', '-0.807', '0.1356', '1.022', '0.1595', '0.3484', '-0.1787', '0.2996', '0.5264', '0.4087', '-0.7856', '0.2805', '-0.548', '-0.00795', '-0.5635', '0.1609', '-0.2092', '0.3596', '-0.273', '0.7344', '-0.34', '0.01556', '0.1536', '-0.4177', '0.1505', '-0.1779', '-0.2544', '-0.5625', '-0.02098', '-0.5264', '-0.308', '-0.1113', '0.001947', '-0.344', '0.273', '0.4521', '-0.41', '0.09503', '0.4158', '-0.1539', '-0.034', '-0.158', '0.333', '-0.407', '-0.083', '-0.346', '0.3313', '-0.0714', '-0.673', '0.01094', '0.04553', '0.1699', '-0.0855', '-0.2747', '0.2693', '0.1862', '0.3303', '0.3162', '0.4988', '-0.2988', '-0.1128', '0.286', '0.596', '-0.03967', '0.2485', '-0.1229', '0.638', '0.0661', '0.2712', '0.665', '-0.521', '0.374', '-0.6797', '0.925', '0.3638']",,,C535559,,,,
mondo:0010555,X-linked chondrodysplasia punctata 1,"['chondrodysplasia punctata 1 X-linked recessive', 'CPXR', 'brachytelephalangic chondrodysplasia punctata', 'chondrodysplasia punctata 1, X-linked recessive', 'CDPX1', 'arylsulfatase E deficiency', 'arse X-linked chondrodysplasia punctata', 'ARSE X-linked chondrodysplasia punctata', 'Cpxr', 'chondrodysplasia punctata brachytelephalangic', 'X-linked chondrodysplasia punctata caused by mutation in arse', 'chondrodysplasia punctata, Brachytelephalangic', 'chondrodysplasia punctata, X-linked recessive, X-linked recessive', 'chondrodysplasia punctata, brachytelephalangic']",,302950,79345,C3669395,"['-0.6875', '0.3357', '0.2048', '-0.6504', '0.1088', '-0.4565', '0.1466', '1.124', '-0.92', '-0.4592', '0.004055', '0.1144', '0.2279', '0.4314', '0.1045', '0.372', '0.1598', '-0.4692', '-0.6074', '-0.805', '0.11847', '-0.2551', '0.9575', '-0.1915', '-0.02872', '0.4229', '-0.2377', '0.3628', '0.02693', '0.3684', '0.0685', '-0.3276', '-0.11945', '-0.02513', '0.3901', '0.2615', '-0.03125', '-0.4963', '-0.2096', '0.073', '0.08136', '-0.2603', '0.10547', '0.165', '-0.182', '-0.238', '-0.3704', '-0.1545', '-0.3062', '-0.08484', '-0.09656', '-0.5117', '0.076', '-0.3953', '-0.4587', '-0.4421', '-0.3982', '0.546', '0.5107', '0.619', '0.561', '0.511', '-0.4128', '0.479', '-0.0633', '0.02477', '0.5425', '0.088', '-0.04605', '0.696', '0.06494', '-0.2468', '-0.163', '-0.521', '-0.3872', '0.4485', '0.04684', '0.4153', '-0.3853', '-0.0823', '-0.517', '0.2305', '-0.04', '0.5493', '0.0958', '0.1696', '-0.267', '-0.1259', '0.551', '-0.1667', '-0.1611', '0.1484', '-0.2496', '0.603', '0.3284', '-0.4053', '0.414', '-0.6304', '0.7275', '0.05716']",,,,,,,
mondo:0010556,X-linked chondrodysplasia punctata,"['chondrodysplasia punctata, X-linked dominant', 'CPXD', 'chondrodystrophia calcificans congenita', 'X-linked dominant chondrodysplasia punctata', 'chondrodysplasia punctata, X-linked']",0060292,,,C0263627,,,,,,,,
mondo:0010557,choroideremia,"['Tapetochoroidal dystrophy', 'CHM', 'choroidal sclerosis', 'choroideremia', 'TCD', 'progressive choroidal atrophy', 'Tapetochoroidal dystrophy, progressive', 'progressive tapetochoroidal dystrophy']",9821,303100,180,C0008525,"['-0.686', '0.1206', '-0.2152', '0.345', '0.1754', '-0.3564', '-0.1163', '0.8438', '-0.6777', '-0.2822', '-0.02681', '-0.139', '0.02379', '0.1866', '0.3757', '-0.001114', '0.0905', '-0.2524', '-0.06494', '-0.8384', '-0.476', '-0.3584', '0.5605', '-0.02748', '0.285', '-0.2866', '0.024', '0.09393', '-0.3567', '1.045', '0.5757', '-0.1149', '0.183', '-0.1029', '0.1626', '0.672', '0.4375', '-0.3972', '0.2496', '-0.4539', '0.423', '-0.827', '0.09595', '0.1509', '0.134', '-0.0889', '-0.10504', '-0.631', '0.1229', '-0.0583', '0.4883', '0.1965', '-0.0922', '-0.11914', '0.455', '0.2542', '0.913', '0.02263', '-0.8726', '-0.1361', '0.1007', '-0.09656', '0.0766', '0.8726', '-0.3867', '0.0775', '0.8896', '0.304', '0.275', '0.742', '-0.519', '-0.1903', '0.2195', '-0.03096', '0.6016', '-0.573', '0.005543', '-0.1185', '0.2029', '-0.3774', '0.633', '-0.4602', '0.0913', '0.9185', '-0.4116', '-0.3171', '-0.0247', '-0.03894', '0.1085', '0.2087', '0.4143', '0.3232', '0.08014', '0.4731', '-0.03854', '-0.3633', '-0.0797', '-0.402', '0.1744', '0.6523']",C34469,,D015794,363.55,H31.21,10008791,
mondo:0010558,choroideremia-deafness-obesity syndrome,"['Ayazi syndrome', 'chromosome Xq21 deletion syndrome', 'choroideremia, deafness, and intellectual disability', 'choroideremia, deafness, and mental retardation', 'Xq21 deletion syndrome, X-linked recessive', 'choroideremia, obesity, and congenital deafness', 'choroideremia deafness obesity']",,303110,1435,C1844836,,,,C537793,,,,
mondo:0010559,MASA syndrome,"['hereditary spastic paraplegia 1', 'MASA syndrome', 'X-linked complicated hereditary spastic paraplegia type 1', 'thumb congenital clasped with mental retardation', 'Clasped thumb and mental retardation', 'spastic paraplegia, X-linked', 'CRASH syndrome, X-linked recessive', 'masa syndrome, X-linked recessive', 'Gareis-Mason syndrome', 'thumb, congenital Clasped, with intellectual disability', 'adducted thumb with intellectual disability', 'thumb, congenital Clasped, with mental retardation', 'spastic paraplegia 1', 'intellectual disability aphasia shuffling Gait adducted thumbs (MASA)', 'mental retardation, aphasia, shuffling Gait, and adducted thumbs', 'X-linked spastic paraplegia 1', 'spastic paraplegia 1, X-linked', 'adducted thumb with mental retardation', 'X-linked corpus callosum agenesis', 'Clasped thumb and intellectual disability', 'CRASH syndrome', 'mental retardation aphasia shuffling Gait adducted thumbs (MASA)', 'thumb congenital clasped with intellectual disability', 'intellectual disability, aphasia, shuffling Gait, and adducted thumbs', 'intellectual disability-aphasia-shuffling gait-adducted thumbs syndrome']",0060246,303350,2466,C0795953,"['-0.0991', '0.256', '0.3337', '-0.5615', '-0.1643', '-0.614', '-0.185', '0.04333', '-0.552', '-0.2727', '-0.3086', '-0.1263', '0.2688', '-0.2267', '0.5415', '-0.3936', '-0.2053', '-0.3264', '0.2418', '-0.698', '0.3525', '0.3093', '0.1433', '-0.2842', '0.2585', '-0.109', '0.1299', '0.3706', '0.1055', '-0.202', '-0.09674', '-0.0688', '0.3835', '0.0804', '-0.3018', '-0.4265', '-0.2316', '-0.0919', '-0.2698', '-0.439', '0.4524', '-0.3528', '-0.2042', '-0.144', '0.0751', '-0.1588', '-0.2798', '-0.06915', '0.014915', '-0.0421', '-0.0501', '-0.0182', '-0.5312', '-0.09186', '0.2524', '-0.1476', '-0.001957', '0.04465', '-0.3425', '0.599', '-0.1993', '-0.05783', '0.5854', '0.2058', '-0.0217', '0.1588', '0.2418', '0.334', '-0.6396', '-0.2089', '-0.4385', '0.2834', '0.3323', '-0.338', '0.1885', '0.3372', '0.1698', '-0.0839', '-0.10767', '-0.252', '-0.1064', '0.08923', '-0.1089', '0.5337', '-0.1613', '0.2637', '-0.1105', '-0.0004492', '0.1971', '0.057', '0.392', '0.599', '0.11786', '0.252', '0.3801', '0.2222', '0.00756', '-0.4688', '0.686', '0.2573']",C129930,,,,,,
mondo:0010560,"cleft palate with or without ankyloglossia, X-linked","['cleft palate with or without ankyloglossia, X-linked', 'CPX', 'X-linked cleft palate and ankyloglossia', 'cleft palate with ankyloglossia', 'cleft palate X-linked', 'cleft palate, X-linked', 'X-linked cleft palate']",0060613,303400,324601,,"['-0.0344', '0.10645', '0.000587', '-0.133', '0.0877', '-0.0996', '2.7e-06', '0.1307', '-0.126', '-0.1324', '-0.02371', '-0.0787', '0.02841', '0.03876', '-0.10144', '-0.05646', '0.0233', '-0.1516', '-0.1154', '-0.1827', '-0.00917', '-0.01019', '0.1328', '-0.03946', '0.0372', '-0.002153', '-0.033', '-0.02963', '0.0724', '-0.1069', '0.0696', '-0.05307', '0.1567', '0.06226', '0.05032', '-0.05786', '-0.011604', '-0.086', '-0.04373', '-0.1794', '0.06775', '-0.1013', '0.05734', '-0.0633', '-0.0824', '-0.1387', '0.02878', '0.091', '-0.02597', '0.04813', '-0.0863', '-0.07336', '0.04922', '0.02078', '-0.0785', '-0.0785', '0.09735', '-0.1067', '-0.1882', '0.00468', '0.0815', '0.07294', '-0.04025', '0.0531', '-0.0353', '-0.015', '0.10144', '0.0734', '-0.09595', '0.149', '-0.12', '0.04257', '0.0695', '-0.1011', '0.02275', '0.03534', '0.03607', '-0.1077', '-0.11896', '-0.05167', '-0.01214', '0.0152', '0.03937', '0.133', '-0.04736', '0.0617', '-0.0227', '0.1871', '0.02718', '0.0498', '-0.01414', '0.162', '0.05838', '0.0849', '0.3137', '-0.003605', '0.1037', '-0.1842', '0.04675', '0.0988']",,,C536426,,,,
mondo:0010561,Coffin-Lowry syndrome,"['Coffin syndrome 1', 'dwarfism, lean spastic type', 'mental retardation with osteocartilaginous abnormalities', 'CLS', 'intellectual disability with osteocartilaginous abnormalities', 'COFFIN-Lowry syndrome', 'Coffin syndrome', 'Coffin-Lowry syndrome', 'lean spastic dwarfism', 'Coffin-Lowry syndrome, X-linked dominant']",3783,303600,192,C0265252,"['0.05283', '0.205', '-0.1514', '-0.202', '0.2498', '-0.1261', '0.2275', '1.007', '-0.6445', '-0.279', '0.1001', '0.0684', '-0.04242', '0.1936', '0.1553', '-0.2715', '0.1771', '-0.368', '-0.294', '-0.4565', '-0.0358', '0.2496', '0.3066', '0.3018', '0.437', '-0.2795', '-0.6274', '0.3342', '0.448', '-0.3542', '0.6245', '-0.3066', '0.06058', '0.205', '-0.1908', '-0.1742', '-0.117', '-0.1021', '0.01617', '-0.138', '-0.05026', '-0.505', '0.3489', '0.557', '0.4893', '-0.534', '0.1451', '-0.0524', '-0.3455', '-0.2084', '-0.0831', '0.1982', '-0.202', '0.1105', '-0.3438', '-0.04764', '0.2563', '-0.344', '0.543', '0.5093', '-0.1399', '-0.02296', '-0.2935', '0.441', '0.3074', '0.1925', '-0.3386', '0.114', '0.02786', '0.3955', '-0.709', '0.4507', '0.1652', '0.10095', '-0.06155', '0.02115', '0.4526', '-0.0611', '-0.2322', '-0.1631', '0.2686', '-0.1642', '-0.529', '0.3667', '0.1501', '0.9595', '-0.3762', '0.02428', '0.489', '0.3132', '0.0469', '0.7236', '-0.271', '0.003626', '0.3835', '0.0998', '0.6265', '-0.5747', '0.4768', '0.4062']",C84643,,D038921,759.89,,,
mondo:0010562,colonic atresia,"['colonic atresia', 'congenital atresia of colon', 'atresia of colon', 'colonic atresia (disease)', 'colon atresia']",,303650,1198,,,C101024,,C562562,,,,0010448
mondo:0010563,blue cone monochromacy,"['colour blindness, blue monocone monochromatic type', 'BCM', 'blue cone monochromacy', 'color blindness blue mono cone monochromatic type', 'cone dystrophy 5, X-linked', 'atypical X-linked achromatopsia', 'color blindness, blue monocone monochromatic type', 'colour blindness blue mono cone monochromatic type', 'achromatopsia incomplete X-linked', 'CBBM', 'incomplete achromatopsia X-linked', 'blue cone monochromacy, X-linked recessive', 'S cone monochromatism', 'X-chromosome-linked achromatopsia', 'colorblindness, blue-Mono-cone-monochromatic type', 'blue cone monochromatism', 'X-linked incomplete achromatopsia', 'X-linked achromatopsia incomplete', 'S cone monochromacy']",0050679,303700,16,CN036572,"['-0.5645', '-0.1187', '0.315', '-0.0281', '0.2009', '-0.002357', '-0.3538', '0.665', '-0.4434', '-0.8716', '0.1544', '-0.0205', '-0.6514', '0.0374', '-0.1267', '-0.209', '0.565', '-0.316', '0.2239', '-0.6445', '-0.7114', '-0.2274', '0.4648', '0.101', '-0.2316', '0.04013', '-0.424', '0.1792', '-0.0686', '0.3987', '0.4119', '0.4473', '0.358', '0.2815', '0.283', '0.1561', '0.07874', '-0.3188', '0.351', '-0.508', '0.4568', '-0.273', '-0.02493', '-0.573', '-0.669', '-0.7075', '-0.1375', '-0.589', '0.2241', '0.118', '0.2642', '-0.11975', '0.4114', '-0.4434', '0.0938', '0.3489', '0.9976', '-0.2312', '-0.5645', '-0.2979', '-0.2532', '0.2302', '0.419', '0.4731', '0.181', '0.01304', '0.6284', '0.2255', '0.01724', '0.1732', '-0.1737', '-0.2952', '-0.275', '-0.3389', '0.8335', '0.05737', '0.5635', '-0.712', '-0.0616', '0.2703', '0.589', '-0.9697', '-0.05466', '1.047', '-0.1528', '-0.1531', '0.02013', '-0.648', '0.2422', '-0.2046', '0.4272', '0.512', '-0.683', '0.4072', '0.753', '0.0112', '-0.4277', '-0.4531', '0.3025', '0.19']",,,C536238,,,,
mondo:0010564,red-green color blindness,"['partial achromatopsia, deutan type', 'Green colorblindness', 'Deuteranomaly', 'deuteranopia', 'Deutan colorblindness', 'Deutan defect', 'CBD', 'colorblindness, deutan', 'colorblindness, partial, DEUTAN series', 'reduced red-green discrimination']",13909,303800,319698,C0155016,"['-0.2196', '-0.2205', '0.688', '0.0645', '-0.05035', '0.1603', '-0.005493', '0.06274', '-0.623', '-0.3853', '0.9043', '-0.3303', '-0.573', '0.44', '0.253', '-0.5635', '-0.0407', '0.35', '-0.4927', '0.019', '-0.7847', '-0.31', '-0.0802', '-0.005527', '0.003149', '-0.5625', '-0.0853', '0.005127', '0.03072', '0.507', '0.422', '-0.614', '0.2637', '0.731', '0.04843', '-0.1284', '-0.305', '-0.667', '0.1517', '-0.7065', '0.3152', '-0.2693', '-0.05035', '-0.2842', '0.1594', '-0.1383', '0.3286', '-0.1617', '1.031', '0.2283', '0.29', '0.3032', '0.554', '-0.505', '0.265', '0.4612', '0.4653', '0.144', '-0.5503', '-0.0996', '-0.6553', '-0.1808', '1.174', '1.021', '0.1189', '0.2262', '0.7896', '0.7285', '-0.4197', '0.671', '0.1959', '0.1542', '-0.0108', '-0.655', '0.07043', '0.2236', '0.1814', '0.02823', '0.09644', '-0.2544', '0.3176', '-0.372', '0.0599', '0.655', '0.077', '-0.4873', '0.2136', '-0.5205', '0.6763', '0.622', '0.1477', '0.1223', '-0.05545', '0.2412', '0.9194', '0.4897', '-0.5684', '-0.3213', '0.02834', '-0.2109']",,0005581,,368.52,H53.53,,
mondo:0010565,red color blindness,"['protan defect', 'CBP', 'partial achromatopsia, protan type', 'red colorblindness', 'colorblindness, protan', 'protanopia', 'colorblindness, partial, protan series', 'protanomaly']",13910,303900,319691,,"['-0.2705', '-0.3687', '0.811', '0.1023', '-0.182', '0.2507', '-0.1876', '-0.0708', '-0.432', '-0.3857', '0.684', '-0.07806', '-0.574', '0.431', '0.371', '-0.4702', '0.0833', '0.298', '-0.405', '0.003527', '-0.857', '-0.11523', '-0.1156', '-0.03973', '0.1367', '-0.3833', '0.003204', '-0.02963', '-0.01814', '0.3472', '0.535', '-0.3557', '0.315', '0.821', '-0.05228', '-0.2394', '-0.161', '-0.5444', '0.136', '-0.7065', '0.2242', '-0.4004', '-0.083', '-0.1566', '0.1326', '-0.1676', '0.2083', '-0.0895', '0.8735', '0.2769', '0.4324', '0.2313', '0.524', '-0.411', '0.2042', '0.2708', '0.5747', '0.284', '-0.4395', '0.03177', '-0.443', '0.063', '0.997', '0.9824', '0.04468', '0.0264', '0.8477', '0.739', '-0.3196', '0.6055', '0.2375', '0.11096', '0.0656', '-0.7017', '0.09924', '0.352', '0.2036', '-0.1414', '0.142', '-0.2966', '0.3872', '-0.3027', '0.1752', '0.603', '0.1045', '-0.569', '0.1294', '-0.4607', '0.7275', '0.5845', '0.3123', '0.074', '0.074', '0.1112', '0.944', '0.3728', '-0.637', '-0.351', '-0.00985', '-0.2358']",,0005580,,368.51,H53.54,,
mondo:0010566,X-linked cone-rod dystrophy 1,"['cone dystrophy 1, X-linked', 'COD1', 'cone-rod dystrophy, X-linked, type 1', 'X-linked cone dystrophy 1', 'CORDX1', 'cone-rod dystrophy, X-linked, 1, X-linked recessive', 'cone-rod dystrophy X-linked 1', 'cone dystrophy X-linked 1', 'X-linked cone-rod dystrophy type 1', 'cone-rod dystrophy, X-linked, 1']",0111008,304020,1872,,"['-0.4465', '-0.5034', '-0.1885', '0.595', '0.1153', '-0.2487', '0.04385', '0.3914', '-0.3533', '0.1514', '0.01355', '-0.1726', '-0.54', '0.5454', '0.6445', '-0.5312', '0.2764', '-0.1815', '0.2048', '-0.6704', '-0.3088', '-0.3386', '0.362', '-0.09924', '-0.4216', '0.02293', '0.0937', '-0.7295', '-0.634', '1.249', '0.7715', '0.0965', '0.3137', '0.587', '0.2024', '-0.243', '-0.3074', '-0.3635', '-0.2515', '-0.5625', '0.07227', '0.1089', '0.2747', '-0.1586', '0.1793', '-0.5073', '-0.0686', '-0.612', '0.2212', '0.515', '0.647', '0.02994', '-0.02469', '-0.4946', '0.1287', '-0.1437', '0.693', '-0.177', '-0.606', '-0.2169', '0.1076', '-0.3967', '0.539', '0.597', '-0.6274', '0.2944', '0.8916', '0.247', '-0.03748', '0.6104', '-0.945', '-0.1776', '-0.1832', '-0.04944', '0.4866', '-0.593', '0.4377', '-0.2559', '-0.3728', '-0.7197', '0.706', '-0.05548', '-0.1146', '0.998', '-0.162', '-0.4326', '0.2898', '-0.3162', '0.4192', '-0.0305', '0.1322', '0.1426', '0.2428', '0.4492', '0.564', '-0.2844', '0.1494', '-0.3262', '0.099', '0.02248']",,,C564438,,,,
mondo:0010567,"cone dystrophy, X-linked, with tapetal-like sheen","['X-linked recessive cone dystrophy with tapetal-like sheen', 'cone dystrophy, X-linked, with tapetal-like sheen', 'cone dystrophy X-linked with tapetal-like sheen']",,304030,,C1844775,,,,C535975,,,,
mondo:0010568,Aicardi syndrome,"['corpus callosum, agenesis of, with chorioretinal Abnormality', 'corpus callosum agenesis of with chorioretinal abnormality', 'Aicardi syndrome, X-linked dominant', 'AIC', 'Aicardi syndrome', 'agenesis of corpus callosum with chorioretinal abnormality']",8461,304050,50,C0175713,,C35256,,D058540,,,10054935,
mondo:0010569,X-linked complicated corpus callosum dysgenesis,"['X-linked complicated corpus callosum agenesis', 'corpus callosum, partial agenesis of, X-linked recessive', 'corpus callosum, partial agenesis of, X-linked', 'X-linked partial corpus callosum agenesis', 'X-linked partial agenesis of corpus callosum']",,304100,1497,C1839909,"['-0.1975', '0.2019', '0.0869', '-0.5415', '-0.1472', '-0.3406', '-0.02405', '0.1794', '-0.3757', '-0.593', '-0.3271', '-0.4075', '-0.01627', '-0.274', '0.3203', '-0.1471', '0.01076', '-0.3218', '0.2106', '-0.7764', '0.3223', '0.231', '0.4744', '-0.161', '0.2505', '0.1208', '-0.02213', '0.1201', '0.3635', '-0.3186', '0.0863', '0.0358', '0.634', '0.1162', '-0.04666', '-0.533', '-0.155', '-0.4626', '-0.2861', '-0.3694', '0.3762', '-0.4006', '-0.1897', '-0.2344', '0.01875', '-0.2764', '-0.07294', '-0.12085', '0.1875', '-0.2361', '0.1559', '-0.1567', '-0.3306', '-0.1815', '-0.237', '0.09045', '-0.04562', '-0.1771', '-0.2427', '0.3445', '-0.1512', '-0.03946', '0.4114', '0.069', '-0.2112', '0.2272', '0.2393', '0.3533', '-0.4434', '0.001437', '-0.3848', '0.0941', '0.04578', '-0.2397', '0.3274', '0.1733', '0.3408', '-0.37', '-0.01572', '-0.2808', '-0.0805', '0.2427', '-0.2428', '0.57', '-0.2878', '0.03156', '0.0128', '0.2837', '0.07227', '0.03763', '0.182', '0.5747', '0.2391', '0.1954', '0.6836', '-0.0845', '0.1998', '-0.2479', '0.4944', '0.298']",,,C564115,,,,
mondo:0010570,craniofrontonasal syndrome,"['craniofrontonasal dysplasia, X-linked dominant', 'craniofrontonasal dysplasia', 'CFNS', 'CFND', 'craniofrontonasal dysostosis', 'craniofrontonasal syndrome']",14737,304110,1520,C0220767,"['0.1929', '0.03455', '0.3325', '-0.2487', '0.312', '0.08563', '-0.0904', '1.183', '-0.977', '-0.8394', '0.0717', '0.3625', '0.005596', '0.107', '-0.1476', '0.2712', '0.3037', '-0.5034', '-0.6997', '-0.3232', '0.0356', '0.463', '0.675', '0.03543', '0.1975', '-0.02483', '0.04968', '0.2993', '0.6455', '-0.4497', '-0.0878', '-0.4563', '-0.0904', '0.2764', '0.08', '0.6396', '-0.0954', '-0.3574', '-0.4634', '-0.6396', '0.433', '0.2937', '0.3555', '-0.1854', '0.4216', '-0.4316', '-0.1566', '0.6333', '-0.0746', '-0.2285', '0.2603', '-0.2172', '0.0907', '-0.10333', '-0.788', '0.0297', '-0.01556', '0.0344', '0.02835', '0.1146', '-0.032', '0.2922', '-0.146', '1.013', '-0.04852', '0.0435', '0.2128', '0.0425', '-0.5884', '0.1471', '0.1682', '0.11334', '0.011024', '-0.2147', '0.05524', '0.333', '0.3494', '-0.0746', '-0.344', '-0.755', '0.1952', '-0.3022', '0.06445', '0.59', '0.03116', '0.4934', '-0.5757', '0.235', '-0.0008864', '0.07623', '-0.4006', '0.7573', '0.5757', '0.534', '0.801', '-0.2656', '0.311', '-0.3015', '0.642', '0.1892']",,,C536456,,,,
mondo:0010571,otopalatodigital syndrome type 2,"['OPD 2 syndrome', 'cranioorodigital syndrome', 'cranio-oro-digital syndrome', 'otopalatodigital syndrome, type 2', 'otopalatodigital syndrome, type II, X-linked dominant', 'OPD syndrome 2', 'OPD2', 'OPD II syndrome', 'Andre syndrome', 'FPO', 'otopalatodigital syndrome, type II', 'oto-palato-digital syndrome type 2', 'faciopalatoosseous syndrome']",0111784,304120,90652,,"['-0.2769', '0.2983', '0.3027', '0.007477', '0.464', '-0.2021', '-0.0466', '0.6953', '-0.79', '-0.526', '-0.148', '-0.6187', '-0.2898', '-0.2646', '-0.57', '-0.0723', '0.231', '-0.2489', '-0.5728', '-0.08887', '0.2646', '0.2996', '0.8267', '-0.3247', '-0.03302', '-0.36', '-0.5586', '0.3113', '0.402', '-0.1757', '0.4424', '-0.3308', '0.4163', '0.1779', '-0.2007', '-0.7236', '-0.00925', '-0.1608', '-0.468', '0.04285', '-0.201', '0.02948', '0.08514', '0.0824', '-0.134', '-0.10315', '0.02011', '0.735', '-0.8643', '0.04556', '0.01505', '0.04083', '-0.4568', '-0.356', '-0.8643', '-0.556', '0.0973', '0.07404', '-0.1498', '-0.1147', '-0.2354', '-0.0614', '-0.04388', '0.644', '-0.2098', '-0.2102', '0.1432', '0.721', '-0.5137', '-0.1705', '-0.3186', '-0.0736', '0.2346', '-0.1992', '-0.2512', '0.2896', '-0.2524', '0.512', '-0.4126', '-0.04843', '-0.4766', '0.01738', '0.276', '0.8154', '-0.1903', '0.8223', '0.04742', '-0.1255', '0.01537', '-0.2773', '-0.2396', '0.5835', '0.669', '0.3079', '0.609', '0.4004', '0.1923', '-0.4502', '0.8013', '0.2627']",,,C538089,759.89,,,
mondo:0010572,occipital horn syndrome,"['EDS IX', 'EDS9, formerly', 'OHS', 'cutis laxa, X-linked', 'EDS IX, formerly', 'cutis laxa, X-linked, formerly', 'Ehlers-Danlos syndrome type IX', 'Ehlers-Danlos syndrome, occipital horn type', 'occipital horn syndrome', 'occipital horn syndrome, X-linked recessive', 'Ehlers-Danlos syndrome type 9', 'Ehlers-Danlos syndrome, occipital horn type (formerly)', 'X-linked cutis laxa', 'Ehlers-Danlos syndrome, occipital horn type, formerly', 'cutis laxa X-linked', 'EDS9', 'EDS IX (formerly)']",0111272,304150,198,,"['-0.1194', '-0.03198', '0.266', '-0.7144', '0.472', '-0.4092', '0.0006595', '1.312', '-0.4202', '0.4197', '-0.1098', '-0.2527', '-0.06213', '0.318', '0.2104', '0.0849', '0.3545', '-0.0805', '-0.1753', '-0.9077', '0.149', '0.3052', '0.2291', '0.2477', '-0.2069', '-0.3213', '0.1901', '0.0167', '-0.079', '-0.1907', '0.2222', '-0.2418', '0.3794', '0.01997', '0.356', '-0.2054', '-0.2961', '-0.2222', '-0.02426', '0.04376', '0.4504', '-0.4739', '0.0786', '0.1992', '0.1663', '0.11957', '0.234', '0.4595', '-0.4663', '0.1675', '-0.1649', '0.6196', '-0.3435', '0.10876', '-0.8164', '-0.2422', '0.5005', '0.459', '0.05396', '-0.3115', '0.3577', '0.551', '-0.5283', '-0.05505', '-0.1672', '0.1711', '-0.04987', '0.5356', '0.02713', '0.9404', '0.159', '0.04617', '-0.3865', '0.2576', '-0.181', '-0.51', '-0.1752', '-0.2761', '-0.74', '-0.5835', '-0.3257', '-0.5728', '0.1611', '0.2317', '0.3872', '0.1648', '-0.1091', '0.099', '-0.05692', '-0.6177', '0.3958', '-0.02692', '-0.1333', '-0.389', '0.404', '0.3708', '0.4778', '-0.4402', '0.4768', '-0.3965']",,,C537860,,,,
mondo:0010573,"cutis verticis gyrata, thyroid aplasia, and intellectual disability","['Akesson syndrome', 'cutis verticis gyrata, thyroaplasia and mental deficiency syndrome', 'cutis verticis gyrata-thyroid aplasia-intellectual disability syndrome', 'cutis verticis gyrata-thyroid aplasia-mental retardation syndrome', 'cutis verticis gyrata, thyroid aplasia, and intellectual disability', 'cutis verticis gyrata, thyroid aplasia, and mental retardation']",,304200,79482,CN237776,,,,C535610,,,,
mondo:0010574,syndromic X-linked intellectual disability 5,"['mental retardation, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures', 'mental retardation X-linked with Dandy-Walker malformation basal ganglia disease and seizures', 'Pettigrew syndrome, X-linked recessive', 'PETTIGREW syndrome', 'X-linked intellectual disability-Dandy-Walker malformation-basal ganglia disease-seizures syndrome', 'PGS', 'X-linked intellectual disability 59', 'intellectual disability X-linked syndromic 5', 'mental retardation, X-linked, syndromic 5', 'fried syndrome', 'mental retardation X-linked syndromic 5', 'mental retardation, X-linked syndromic 5', 'X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behavior syndrome', 'mental retardation, X-linked 59', 'syndromic X-linked mental retardation fried type', 'mental retardation, X-linked, syndromic 21', 'X-linked intellectual disability-hypotonia-facial dysmorphism-aggressive behaviour syndrome', 'syndromic X-linked mental retardation 21', 'intellectual disability, X-linked, syndromic 5', 'intellectual disability, X-linked, with Dandy-Walker malformation, basal ganglia disease, and seizures', 'Pettigrew syndrome', 'MRXS5', 'X-linked mental retardation 59', 'intellectual disability, X-linked syndromic 5', 'syndromic X-linked intellectual disability type 5', 'X-linked metal retardation with Dandy-Walker malformation, basal ganglia disease, and seizures', 'intellectual disability, X-linked, syndromic, fried type', 'syndromic X-linked intellectual disability 21', 'Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures', 'intellectual disability, X-linked 59', 'X-linked intellectual disability - Dandy-Walker malformation - basal ganglia disease - seizures', 'MRX59', 'MRXS21', 'syndromic X-linked intellectual disability fried type', 'intellectual disability X-linked with Dandy-Walker malformation basal ganglia disease and seizures', 'intellectual disability, X-linked, syndromic 21', 'mental retardation, X-linked, syndromic, fried type']",0060800,304340,85335,CN206181,"['-0.303', '0.427', '0.427', '-0.69', '0.10736', '-0.647', '-0.03415', '0.294', '-0.8115', '-0.014656', '-0.605', '-0.2192', '0.04587', '-0.61', '-0.328', '-0.3813', '0.2495', '-0.566', '-0.1943', '-0.547', '0.2603', '-0.1606', '0.2954', '0.2512', '-0.259', '-0.2115', '0.06042', '-0.4512', '-0.3386', '-0.2327', '0.1422', '0.1196', '0.9746', '-0.05328', '0.283', '-0.02682', '-0.4807', '-0.5703', '0.03934', '-0.3777', '0.2788', '-0.6885', '0.132', '0.096', '0.004417', '-0.3254', '0.5303', '0.4836', '-0.1683', '-0.4648', '0.01064', '0.7764', '0.2654', '-0.1539', '-0.2125', '-0.0324', '-0.2573', '0.3552', '-0.4136', '0.2148', '-0.1139', '-0.3877', '-0.139', '-0.002058', '-0.3574', '0.08496', '0.932', '0.279', '-0.4714', '0.1038', '-0.4626', '0.4014', '0.2488', '0.1593', '-0.4114', '-0.1033', '0.3604', '-0.1826', '-0.3486', '-0.2251', '-0.3354', '-0.05524', '-0.2651', '0.5273', '0.3508', '-0.2593', '-0.0343', '0.2217', '0.1129', '0.12067', '0.6074', '0.567', '0.519', '0.3577', '0.3062', '0.558', '0.01862', '-0.0953', '0.781', '0.4875']",C124839,,,,,,
mondo:0010575,deafness-hypogonadism syndrome,"['deafness-hypogonadism syndrome', 'deafness hypogonadism syndrome', 'DHS']",,304350,90646,,,,,C564435,,,,
mondo:0010576,X-linked mixed hearing loss with perilymphatic gusher,"['deafness mixed with perilymphatic gusher', 'high frequency hearing loss', 'DFN 3 nonsyndromic hearing loss and deafness', 'perilymphatic gusher-deafness syndrome', 'sensorineural deafness, profound, with or without a conductive component, associated with a unique developmental Abnormality of the Ear', 'high frequency deafness', 'X-linked mixed deafness with perilymphatic gusher', 'deafness, X-linked 2', 'high-frequency hearing loss', 'X-linked stapes gusher syndrome', 'X-linked mixed conductive and sensorineural hearing loss', 'Nance deafness', 'DFNX2', 'X-linked mixed conductive and neurosensory hearing loss', 'deafness conductive with stapes fixation', 'deafness 3, conductive, with stapes fixation', 'perceptive deafness', 'perceptive hearing loss or deafness', 'sensorineural hearing loss', 'gusher syndrome', 'deafness, conductive, with stapes fixation', 'deafness, mixed, with perilymphatic gusher', 'central hearing loss', 'deafness mixed with perilymphatic gusher, X-linked', 'X-linked mixed conductive and neurosensory deafness', 'perceptive hearing loss', 'deafness 3 conductive with stapes fixation', 'sensorineural deafness', 'X-linked mixed conductive and sensorineural deafness', 'conductive deafness with stapes fixation', 'deafness, X-linked 2, X-linked recessive', 'sensory hearing loss', 'deafness, X-linked type 2', 'DFN3', 'X-linked deafness type 2']",10003,304400,383,C1844678,"['-0.02936', '0.04584', '0.2325', '-0.1956', '0.379', '-0.00587', '0.1532', '0.4062', '-0.01311', '0.1578', '-0.2179', '-0.5215', '-0.193', '0.0844', '0.011894', '-0.267', '0.02797', '0.03836', '-0.0928', '-0.336', '-0.2827', '-0.02596', '0.2413', '-0.084', '0.2964', '0.1234', '-0.37', '-0.1285', '0.148', '-9.495e-05', '0.3423', '-0.038', '0.2622', '0.1394', '-0.11816', '-0.4639', '-0.07404', '-0.5347', '-0.1309', '-0.6387', '-0.04037', '-0.04153', '0.10297', '-0.05655', '0.02455', '-0.453', '-0.1129', '-0.03488', '-0.2693', '0.4258', '0.1302', '-0.1808', '-0.08167', '-0.1659', '-0.1797', '0.1638', '0.4504', '-0.03622', '-0.1788', '0.11676', '-0.2388', '-0.0913', '-0.04175', '0.5376', '-0.1638', '-0.09076', '-0.07996', '0.3787', '-0.1716', '0.3413', '-0.3662', '0.12085', '0.209', '-0.4084', '-0.05164', '-0.1843', '0.333', '0.1177', '-0.1318', '-0.2783', '0.01862', '-0.1613', '0.2778', '0.3923', '-0.1569', '0.006958', '-0.05548', '0.4927', '-0.1508', '0.1814', '-0.06396', '0.577', '0.01445', '0.11285', '0.5947', '-0.2778', '0.277', '-0.424', '0.2306', '0.2375']",,1001176,,389.14,,10040016,
mondo:0010577,"hearing loss, X-linked 1","['deafness, X-linked 2, sensorineural congenital', 'deafness, X-linked 1', 'DFNX1', 'deafness, X-linked type 1']",0111739,304500,,C1844677,,,,C564433,,,,
mondo:0010578,deafness dystonia syndrome,"['DDP', 'DDON syndrome', 'Mohr-Tranebjaerg syndrome, X-linked recessive', 'dystonia deafness syndrome', 'deafness dystonia optic neuronopathy syndrome', 'deafness-Dystonia-optic atrophy syndrome', 'MOHR-Tranebjaerg syndrome', 'dystonia-deafness syndrome', 'MTS', 'Mohr-Tranebjaerg syndrome', 'deafness syndrome, progressive, with blindness, dystonia, fractures, and mental deficiency', 'deafness - dystonia - optic neuronopathy syndrome', 'deafness dystonia optic atrophy syndrome', 'deafness-dystonia-optic neuronopathy (DDON) syndrome', 'deafness-dystonia-optic neuronopathy syndrome', 'deafness dystonia optic neuronopathy syndrome (DDON)']",0050757,304700,52368,C0796074,"['0.8774', '0.589', '-0.203', '-0.1835', '-0.2126', '-1.086', '0.3657', '0.5986', '-0.4736', '-0.1505', '0.845', '0.504', '-0.3604', '0.1323', '0.642', '0.1962', '-0.2217', '-0.4583', '-0.3743', '-0.619', '-0.2192', '-0.3442', '-0.4883', '-0.02466', '-0.2598', '0.268', '-0.4412', '0.0639', '-0.3462', '0.2249', '0.565', '0.6187', '0.7065', '0.1444', '0.012535', '-0.2173', '0.04636', '-0.2415', '0.10583', '-0.3025', '0.479', '0.2961', '-0.04556', '-0.224', '0.4624', '-0.297', '-0.4167', '-0.2727', '-0.0677', '0.422', '0.2484', '0.0968', '0.8223', '-0.3354', '0.607', '-0.0596', '0.628', '0.3142', '0.1575', '-0.314', '-0.7446', '-0.5034', '0.00507', '-0.07886', '-0.6914', '0.5933', '-0.0479', '0.4395', '-0.343', '0.297', '-0.563', '-0.0979', '-0.1975', '-0.1981', '0.6367', '0.1096', '0.9517', '-0.4087', '-0.003159', '-0.2035', '0.10486', '-0.1159', '0.3215', '0.717', '0.4858', '0.105', '-0.035', '0.163', '1.016', '0.3743', '0.398', '0.6694', '0.2417', '0.3499', '0.6094', '-0.5767', '-0.146', '-0.1301', '0.8643', '0.09045']",,,C535808,759.89,,,
mondo:0010579,X-linked corneal dermoid,"['Guizar-Vazquez Luengas-Munoz syndrome', 'bilateral corneal dermoids', 'Guízar Vázquez-Luengas-muñoz syndrome', 'corneal dermoids and short stature', 'dermoids of cornea', 'CND', 'corneal dystrophy epithelial-short stature syndrome']",,304730,1661,C1844671,,,,C535376,,,,
mondo:0010580,immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome,"['diarrhea, polyendocrinopathy, fatal infection syndrome, X-linked', 'Iddm-secretory diarrhea syndrome', 'polyendocrinopathy, immune dysfunction and diarrhea X-linked', 'immunodeficiency, polyendocrinopathy, and enteropathy, X-linked', 'IPEX', 'diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhoea', 'IDDM-secretory diarrhea syndrome', 'diabetes mellitus, congenital insulin-dependent, with fatal secretory diarrhea', 'polyendocrinopathy, immune dysfunction, and diarrhea, X-linked', 'IDDM-secretory diarrhoea syndrome', 'autoimmunity-immunodeficiency syndrome X-linked', 'autoimmune enteropathy type 1', 'DMSD', 'XLAAD', 'Immunodysregulation, polyendocrinopathy and enteropathy X-linked', 'IDDM secretory diarrhoea syndrome', 'immunodysregulation, polyendocrinopathy, and enteropathy, X-linked', 'IDDM secretory diarrhea syndrome', 'IMMUNODYSREGULATION, polyendocrinopathy, and enteropathy, X-linked', 'autoimmunity-immunodeficiency syndrome, X-linked', 'Iddm-secretory diarrhoea syndrome', 'X-linked autoimmunity-allergic dysregulation syndrome', 'immune dysfunction and diarrhoea syndrome', 'enteropathy, autoimmune, with hemolytic Anaemia and polyendocrinopathy', 'immunodysregulation, polyendocrinopathy, and enteropathy, X-linked, X-linked recessive', 'islets of Langerhans, absence of', 'IPEX syndrome', 'immune dysfunction and diarrhea syndrome', 'immunodeficiency, polyendocrinopathy, and enteropathy, X-linked, formerly', 'polyendocrinopathy, immune dysfunction and diarrhoea X-linked', 'X linked polyendocrinopathy', 'XPID', 'immune dysregulation, polyendocrinopathy, and enteropathy X-linked syndrome', 'enteropathy, autoimmune, with hemolytic Anemia and polyendocrinopathy']",0090110,304790,37042,,"['-0.02022', '0.3508', '-0.2017', '-0.2053', '0.2421', '-0.3572', '0.2294', '-0.1069', '-0.2057', '-0.4502', '-0.3215', '-0.162', '-0.5737', '0.1061', '-0.05087', '0.03012', '-0.1121', '0.05054', '-0.1887', '-0.9077', '-0.0012', '-0.5767', '0.785', '-1.052', '0.09656', '0.1573', '-0.503', '-0.0895', '-0.0872', '-0.629', '0.662', '0.0699', '0.2783', '0.563', '0.405', '0.10583', '-0.3662', '-0.528', '-0.621', '0.309', '-0.1544', '0.5845', '0.3445', '0.4346', '0.3914', '-0.3462', '-0.1622', '0.04788', '-0.645', '0.0805', '-0.3796', '0.3572', '0.916', '-0.07684', '-0.3928', '0.1906', '0.0191', '-0.6978', '-0.4539', '0.364', '0.3413', '0.4187', '0.2764', '0.208', '0.01997', '-0.1694', '0.621', '0.1344', '-0.01976', '0.6294', '-0.4746', '-0.765', '0.06757', '-0.1781', '0.2927', '-0.376', '-0.326', '-0.09216', '0.631', '0.172', '-0.2247', '-0.2222', '-0.2554', '0.1572', '-0.04175', '0.8267', '0.5327', '0.413', '0.3887', '0.1238', '0.8096', '0.18', '0.1675', '-0.4973', '0.3638', '0.678', '-0.04077', '-0.531', '0.6216', '0.1277']",C131009,,C580192,250.81,E31.0,,
mondo:0010581,"diabetes insipidus, nephrogenic, X-linked","['Ndi', 'diabetes insipidus, nephrogenic, 1, X-linked recessive', 'diabetes insipidus, nephrogenic, X-linked', 'diabetes insipidus, nephrogenic, type 1']",0081060,304800,,C1563705,,,,,,,,
mondo:0010583,"Dyggve-Melchior-Clausen syndrome, X-linked","['X-linked Dyggve-Melchior-Clausen disease', 'Dyggve-Melchior-Clausen syndrome, X-linked', 'Dyggve-Melchior-Clausen disease, X-linked']",,304950,,C1844654,,,,,,,,
mondo:0010584,"dyskeratosis congenita, X-linked","['DKCX', 'Hoyeraal Hreidarsson syndrome', 'dyskeratosis congenita, X-linked, X-linked recessive', 'dyskeratosis congenita, X-linked', 'Zinsser-Cole-Engman syndrome', 'dyskeratosis congenita X-linked', 'cerebellar hypoplasia with pancytopenia', 'Growth retardation, prenatal, with progressive pancytopenia and cerebellar hypoplasia', 'X-linked dyskeratosis congenita']",0070025,305000,,,"['-0.0609', '0.05994', '0.01428', '-0.06537', '0.0324', '-0.06073', '0.00692', '0.04056', '-0.04797', '-0.0533', '-0.02875', '-0.00799', '-0.009125', '-0.0034', '-0.00349', '-0.011314', '0.01851', '-0.0386', '-0.0427', '-0.1255', '-0.03128', '-0.01653', '0.06192', '-0.0234', '0.001581', '0.00942', '-0.015434', '-0.03067', '0.0221', '-0.06573', '0.04678', '0.012596', '0.0807', '0.02736', '0.02527', '0.003128', '-0.02039', '-0.02856', '-0.02191', '-0.0637', '-0.010635', '-0.0932', '0.01393', '-0.01788', '0.005413', '-0.0651', '-0.01636', '0.02855', '0.02945', '0.007904', '0.00684', '0.01032', '0.00977', '-0.00864', '-0.05035', '-0.03906', '0.04947', '-0.02638', '-0.0815', '0.00822', '0.0398', '0.008606', '0.004948', '0.02408', '0.02939', '-0.00566', '0.0717', '0.05692', '-0.0539', '0.07556', '-0.06616', '-0.01255', '0.02794', '-0.035', '0.01436', '0.03897', '0.01115', '-0.01686', '-0.02937', '-0.05228', '0.002588', '0.02126', '-0.0414', '0.055', '-0.00751', '0.02324', '0.01913', '0.03778', '0.0483', '0.02919', '0.02437', '0.03918', '-0.002903', '0.0228', '0.11646', '0.02672', '0.05917', '-0.0935', '0.02356', '0.01988']",C126352,,,,,,
mondo:0010585,X-linked hypohidrotic ectodermal dysplasia,"['hypohidrotic ectodermal dysplasia, X-linked', 'anhidrotic ectodermal dysplasia X-linked', 'ectodermal dysplasia 1, hypohidrotic/hair/Tooth type, X-linked', 'hypohidrotic ectodermal dysplasia X-linked', 'ectodermal dysplasia, anhidrotic, X-linked', 'Xlhed', 'CST syndrome', 'ectodermal dysplasia 1', 'ectodermal dysplasia 1, hypohidrotic, X-linked, X-linked recessive', 'Eda1', 'X-linked anhidrotic ectodermal dysplasia', 'XHED', 'ectodermal dysplasia 1, hypohidrotic, X-linked', 'ectodermal dysplasia, hypohidrotic, 1', 'Christ-Siemens-Touraine syndrome']",0111664,305100,181,,"['-0.2595', '0.2517', '0.1322', '-0.01481', '0.4185', '-0.145', '-0.05392', '0.05', '-0.1638', '-0.3687', '-0.08057', '0.00339', '-0.1398', '0.01154', '0.0219', '-0.07465', '-0.1197', '-0.12054', '-0.3086', '-0.4226', '-0.1276', '0.0679', '0.5713', '-0.3025', '0.131', '0.01011', '-0.0952', '-0.1543', '0.2145', '-0.324', '0.1752', '0.2417', '0.006306', '-0.04086', '0.011154', '-0.3103', '0.024', '-0.2063', '-0.0745', '-0.4119', '-0.0365', '-0.3103', '-0.01773', '-0.1705', '-0.2612', '-0.2607', '0.07855', '-0.08105', '0.441', '-0.3203', '0.1865', '-0.255', '0.05984', '0.05417', '0.000696', '-0.4036', '0.4946', '0.0687', '-0.3716', '0.093', '0.1464', '0.08575', '0.07104', '0.0593', '0.0478', '0.1838', '0.1748', '0.142', '-0.3904', '0.03613', '-0.4023', '-0.12103', '0.0591', '0.174', '0.03864', '-0.00911', '0.06174', '0.296', '-0.2028', '-0.1927', '0.0535', '0.04602', '0.0975', '0.27', '-0.11896', '0.002928', '0.1986', '0.4583', '0.1398', '0.2272', '-0.1261', '0.422', '-0.0839', '0.000727', '0.584', '0.03836', '0.2927', '-0.472', '0.079', '0.1311']",,,,,,,
mondo:0010586,X-linked Ehlers-Danlos syndrome,"['EDS V', 'EDS 5', 'EDS5', 'Ehlers-Danlos syndrome, X-linked', 'Ehlers-Danlos syndrome, type 5', 'Ehlers-Danlos syndrome type 5', 'Ehlers-Danlos syndrome, type V']",,305200,75497,C0268341,,C141423,,C536197,,,,
mondo:0010587,"epidermodysplasia verruciformis, X-linked","['EDVX', 'X-linked epidermodysplasia verruciformis', 'EDV2', 'epidermodysplasia verruciformis, X-linked']",,305350,,C1844589,,,,C564430,,,,
mondo:0010588,"exudative vitreoretinopathy 2, X-linked","['exudative vitreoretinopathy caused by mutation in NDP', 'Evrx', 'exudative vitreoretinopathy 2, X-linked, X-linked recessive, X-linked dominant', 'NDP exudative vitreoretinopathy', 'exudative vitreoretinopathy 2, X-linked', 'Fevr, X-linked', 'EVR2', 'exudative vitreoretinopathy, familial, 2']",0111413,305390,,C1844579,,,,C564428,,,,
mondo:0010589,"Aarskog-Scott syndrome, X-linked","['MRXS16, included', 'faciogenital dysplasia', 'faciodigitogenital syndrome, recessive', 'mental retardation, X-linked, syndromic 16, included', 'AAS', 'Aarskog-Scott syndrome', 'Scott Aarskog syndrome', 'Aarskog-like syndrome', 'Aarskog-Scott syndrome, X-linked recessive', 'FGDY', 'mental retardation, X-linked syndromic 16, X-linked recessive', 'mental retardation, X-linked, syndromic 16', 'faciogenital dysplasia with attention Deficit-hyperactivity disorder', 'FGD', 'Aarskog syndrome, X-linked', 'Aarskog disease', 'facio-digito-genital dysplasia', 'Aarskog Scott syndrome', 'Aarskog syndrome', 'faciodigitogenital syndrome']",6683,305400,915,,,C129720,,C535331,759.89,,10067148,
mondo:0010590,FG syndrome 1,"['FG syndrome type 1', 'intellectual disability, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum', 'FG syndrome', 'Keller syndrome', 'FG syndrome caused by mutation in MED12', 'Opitz-Kaveggia syndrome, X-linked recessive', 'MED12 FG syndrome', 'Opitz-Kaveggia syndrome', 'FG syndrome 1', 'mental retardation, large head, imperforate anus, congenital hypotonia, and partial agenesis of corpus callosum', 'OKS']",,305450,93932,C0220769,,,,,,,,
mondo:0010591,fingerprint body myopathy,['fingerprint body myopathy'],,305550,97232,C1844560,,,,C564425,,,,
mondo:0010592,focal dermal hypoplasia,"['focal dermal hypoplasia, X-linked dominant', 'focal dermal hypoplasia', 'Goltz syndrome', 'Fodh', 'Goltz-Gorlin syndrome', 'DHOF', 'Goltz Gorlin syndrome', 'FDH']",2120,305600,2092,C0016395,"['0.1599', '0.1925', '-0.1205', '-0.2988', '-0.0387', '0.498', '-0.1649', '0.624', '-0.1998', '-0.1133', '-0.6895', '-0.4111', '0.04242', '-0.126', '-0.609', '0.555', '0.4336', '-0.4834', '-0.7607', '-0.835', '-0.2207', '0.3337', '0.836', '-0.1766', '-0.1556', '-0.6953', '-0.5093', '-0.0368', '0.8633', '-0.1366', '0.635', '0.01262', '-0.09784', '-0.0927', '0.4614', '-0.1161', '-0.3442', '-0.2048', '-0.2382', '-0.1622', '0.0765', '-0.3035', '0.0917', '-0.0785', '0.8228', '-0.793', '-0.05612', '0.3538', '-0.506', '-0.3118', '-0.1632', '0.10706', '0.2341', '0.10974', '-0.8843', '-0.06366', '0.1398', '-0.6865', '-0.2009', '-0.216', '-0.1428', '-0.2944', '-0.4983', '0.015564', '-0.3242', '-0.0004704', '0.94', '0.511', '0.0758', '0.724', '-0.1722', '0.0537', '-0.4622', '0.361', '-0.339', '-0.2795', '0.2742', '-0.2512', '-0.08606', '0.10345', '0.151', '0.3625', '0.54', '0.6924', '0.01953', '-0.279', '-0.04504', '0.1215', '-0.12103', '-0.1433', '0.0695', '-0.02641', '0.6484', '0.3416', '0.8574', '0.263', '0.526', '-0.1415', '0.5796', '0.2286']",C84715,,D005489,757.39,,,
mondo:0010595,Sertoli cell-only syndrome,"['DEL CASTILLO syndrome', 'Del Castillo syndrome', 'Sertoli cell-only syndrome', 'Germinal cell aplasia']",0050457,,,,,C168988,1001422,D054331,752.89,,,
mondo:0010596,"membranoproliferative glomerulonephritis, X-linked","['Mesangiocapillary glomerulonephritis, X-linked', 'membranoproliferative glomerulonephritis, X-linked']",,305800,,C1844501,,,,C564423,,,,
mondo:0010597,glutamyl ribose-5-phosphate storage disease,"['glutamyl ribose-5-phosphate storage disease', 'ADP-ribose Protein hydrolase deficiency']",,305920,,C1844440,,,,C564422,,,,
mondo:0010598,glycogen storage disease IXa1,"['GSD VIII, formerly', 'glycogenosis type 9A', 'glycogen storage disease 8', 'glycogen storage disease VIII', 'GSD9A1', 'glycogen storage disease caused by mutation in PHKA2', 'glycogenosis type IXa', 'hepatic glycogen phosphorylase kinase deficiency', 'GSD type 9A', 'glycogen storage disease type IXa', 'glycogen storage disease IXa', 'glycogen storage disease, type IXa2, X-linked recessive', 'glycogen storage disease type VIII', 'glycogen storage disease type 9A', 'PHKA2-related glycogen storage disease type IX', 'glycogen storage disease, type IXa1, X-linked recessive', 'GSD9A', 'GSD VIII', 'glycogenosis type VIII', 'glycogen storage disease IXa1', 'GSD type IXa', 'glycogen storage disease VIII, formerly', 'PHKA2 glycogen storage disease', 'PYKL', 'phosphorylase kinase deficiency of liver', 'hepatic phosphorylase kinase deficiency', 'glycogenosis type 8', 'liver glycogenosis, X-linked, type 1']",2751,306000,,C0017927,,,1000952,D006015,,,10053242,
mondo:0010599,"granulomas, congenital cerebral","['granulomas, congenital cerebral', 'congenital cerebral granulomas']",,306300,,C1844406,,,,C537294,,,,
mondo:0010600,"granulomatous disease, chronic, X-linked","['chronic granulomatous disease, X-linked', 'cytochrome B-negative granulomatous disease, chronic, X-linked', 'chronic granulomatous disease, atypical', 'granulomatous disease, chronic, X-linked, variant', 'cytochrome B-positive granulomatous disease, chronic, X-linked', 'CGD', 'granulomatous disease, chronic, autosomal dominant type', 'granulomatous disease, chronic, X-linked', 'CDGX', 'chronic granulomatous disease, X-linked, X-linked recessive']",0070195,306400,,C1841825,,,,C564210,,,,
mondo:0010602,hemophilia A,"['Haemophilia A', 'HEMA', 'haemophilia a, X-linked recessive', 'autosomal hemophilia a', 'congenital factor VIII disorder', 'factor 8 deficiency', 'classic haemophilia', 'classical haemophilia', 'hemophilia A', 'hemophilia A, congenital', 'autosomal haemophilia a', 'haemophilia type a', 'haemophilia A, congenital', 'classical hemophilia', 'factor VIII deficiency', 'hemophilia a, X-linked recessive', 'classic hemophilia', 'hemophilia, classic', 'hemophilia type A', 'hem A', 'hemophilia type a', 'hereditary Factor VIII deficiency disease', 'Subhemophilia', 'haemophilia type A', 'hereditary Factor VIII deficiency']",12134,306700,98878,CN239112,"['-0.3318', '-0.005146', '-0.979', '-0.324', '-0.5317', '0.543', '-0.06216', '0.4348', '-0.733', '0.2708', '0.1973', '0.001176', '0.325', '0.2944', '-0.6294', '-0.01196', '-0.699', '0.3289', '-0.2913', '-1.144', '-0.1048', '-0.11237', '0.4702', '-0.07214', '-0.4285', '-0.971', '-0.4592', '-0.04254', '0.4717', '-0.05338', '0.665', '-0.1412', '0.933', '-0.1626', '-0.1549', '0.05368', '-0.332', '0.08185', '0.2598', '-0.4658', '0.569', '0.03174', '-0.34', '-0.3647', '0.2764', '0.7217', '-0.3728', '-0.1208', '0.664', '1.013', '0.1016', '-0.3352', '0.2091', '0.1619', '-0.4617', '0.1467', '-0.1941', '0.3733', '-0.614', '0.02338', '-0.836', '-0.3535', '0.3057', '0.6685', '0.07074', '0.2598', '0.2676', '0.281', '-0.9375', '0.1593', '-0.2852', '-0.0555', '-0.2712', '-1.163', '1.0625', '0.6484', '0.1461', '0.7363', '0.5576', '-0.1384', '-0.3723', '-0.3184', '0.315', '-0.6245', '-0.458', '0.3518', '0.1956', '0.1958', '0.1098', '-0.4473', '-0.531', '0.8022', '-0.07764', '-0.629', '0.2637', '0.8726', '-0.4565', '-0.7866', '0.389', '-0.3733']",C27146,0007267,D006467,286.0,,10016080,
mondo:0010603,hemophilia A with vascular abnormality,['hemophilia A with vascular abnormality'],,306800,,C1844137,,,,C564415,,,,
mondo:0010604,hemophilia B,"['hemophilia B(M)', 'haemophilia type B', 'hem B', 'haemophilia b, X-linked recessive', 'plasma thromboplastin component deficiency', 'congenital factor IX disorder', 'factor 9 deficiency', 'F9 deficiency', 'hemophilia B Leyden', 'haemophilia B(M)', 'hemophilia B', 'hereditary Factor IX deficiency', 'hemophilia type B', 'congenital factor IX deficiency', 'deficiency, functional factor IX', 'hereditary Factor IX deficiency disease', 'haemophilia B Leyden', 'HEMB', 'hemophilia b, X-linked recessive', 'factor IX deficiency', 'Christmas disease']",12259,306900,98879,C0008533,"['-0.3887', '0.02245', '-0.9805', '-0.382', '-0.4866', '0.4329', '-0.175', '0.1904', '-0.593', '0.1803', '0.2517', '-0.1119', '0.3333', '0.4302', '-0.5396', '0.03464', '-0.755', '0.2', '-0.396', '-0.9414', '0.05344', '-0.00174', '0.4417', '0.0383', '-0.274', '-1.027', '-0.3958', '-0.001848', '0.414', '0.03122', '0.636', '-0.146', '0.882', '-0.1532', '-0.2383', '-0.0747', '-0.417', '0.0828', '0.226', '-0.5635', '0.5576', '0.1368', '-0.4392', '-0.2147', '0.3848', '0.6665', '-0.297', '-0.1477', '0.534', '0.8438', '0.2295', '-0.2491', '0.06073', '0.2246', '-0.489', '0.2258', '-0.0615', '0.4048', '-0.5522', '0.07227', '-0.838', '-0.3079', '0.3438', '0.576', '0.1276', '0.3896', '0.1528', '0.3896', '-0.9414', '0.0951', '-0.3196', '0.0689', '-0.3474', '-1.236', '0.9946', '0.5615', '0.2357', '0.7266', '0.4128', '-0.28', '-0.4893', '-0.2866', '0.2761', '-0.685', '-0.4507', '0.205', '0.1884', '0.1483', '0.2144', '-0.536', '-0.5073', '0.926', '-0.09766', '-0.544', '0.2976', '0.8994', '-0.5522', '-0.647', '0.602', '-0.344']",C26721,0009154,D002836,286.1,,10016077,
mondo:0010605,hemopoietic proliferation,['hemopoietic proliferation'],,306930,,,,,,,,,,
mondo:0010606,"hernia, anterior diaphragmatic","['hernia, anterior diaphragmatic']",,306950,,,,,,C564413,,,,
mondo:0010607,"heterotaxy, visceral, 1, X-linked","['congenital heart defects, nonsyndromic, 1, X-linked, X-linked recessive', 'congenital heart defects, multiple types, 1, X-linked', 'visceral heterotaxy caused by mutation in ZIC3', 'heterotaxy, visceral, 1, X-linked, X-linked recessive', 'X-linked visceral heterotaxy 1', 'HTX1', 'laterality, X-linked', 'situs inversus, Complex Cardiac defects, and splenic defects, X-linked', 'ZIC3 visceral heterotaxy', 'heterotaxy, visceral, X-linked', 'heterotaxy, visceral, 1, X-linked', 'dextrocardia with Other Cardiac malformations']",,306955,,C1844020,,,0009136,C538116,,,,
mondo:0010608,Hhhh syndrome,"['hereditary Hemihypotrophy hemiparesis hemiathetosis syndrome', 'Hhhh syndrome']",,306960,,C1844019,,,,C564411,,,,
mondo:0010610,holoprosencephaly-hypokinesia-congenital contractures syndrome,"['holoprosencephaly-fetal akinesia/hypokinesia sequence syndrome', 'holoprosencephaly with foetal akinesia/hypokinesia sequence', 'Morse-Rawnsley-Sargent syndrome', 'holoprosencephaly with fetal akinesia/hypokinesia sequence']",,306990,2570,,,,,C564409,,Q04.2,,
mondo:0010611,X-linked hydrocephalus with stenosis of the aqueduct of Sylvius,"['hydrocephalus with hirschsprung disease, X-linked recessive', 'XLAS', 'HSAS', 'hydrocephalus due to congenital stenosis of aqueduct of Sylvius', 'hydrocephalus, X-linked, with congenital idiopathic intestinal pseudoobstruction', 'X-linked hydrocephalus', 'Bickers-Adams syndrome', 'HSAS1', 'aqueductal stenosis, X-linked', 'X-linked HSAS', 'X-linked hydrocephalus with stenosis of aqueduct of Sylvius', 'hydrocephalus with stenosis of the aqueduct of Sylvius', 'X-linked acqueductal stenosis', 'hydrocephalus with congenital idiopathic intestinal pseudoobstruction, X-linked recessive', 'hydrocephalus due to aqueductal stenosis, X-linked recessive', 'HYCX', 'hydrocephalus, X-linked']",,307000,2182,,"['-0.0023', '-0.05548', '0.3325', '-0.001453', '-0.231', '-0.3435', '-0.2152', '0.521', '-0.3801', '0.3467', '-0.1774', '-0.9355', '-0.2578', '0.3076', '0.508', '-0.2426', '-0.382', '0.2086', '-0.5137', '-1.03', '-0.12286', '-0.2025', '0.4233', '-0.1199', '-0.0676', '-0.4697', '-0.7915', '1.193', '-0.3198', '0.527', '-0.4656', '-0.985', '0.5493', '-0.11816', '-0.365', '0.346', '-0.2744', '0.001982', '0.03114', '-0.4822', '0.9766', '0.02078', '0.01086', '-0.5747', '0.7915', '0.00302', '0.311', '-0.728', '0.4604', '0.396', '0.1411', '0.07135', '-0.3665', '-0.912', '0.3271', '-0.08624', '-0.00701', '0.10876', '0.2296', '0.6123', '-0.5757', '0.3499', '-0.405', '-0.0884', '0.00506', '0.1747', '-0.1416', '0.1344', '-0.903', '0.2451', '0.10333', '1.186', '0.3936', '-0.8584', '0.3308', '0.4717', '0.2983', '0.767', '-0.1953', '-1.079', '-0.744', '-0.1167', '-0.2986', '0.4224', '0.2515', '1.166', '0.5684', '0.2349', '0.2656', '-0.6997', '0.0783', '0.8423', '0.3123', '0.04303', '0.6367', '0.4243', '0.658', '-0.2415', '0.02364', '0.222']",,,C536078,,,,
mondo:0010612,hydrocephaly-cerebellar agenesis syndrome,"['hydrocephalus with cerebellar agenesis', 'X-linked hydrocephalus-cerebellar agenesis-intellectual disability syndrome', 'cerebellum agenesis hydrocephaly']",,307010,1397,C1844005,,,,C564407,,,,
mondo:0010613,inborn glycerol kinase deficiency,"['hyperglycerolemia', 'GK deficiency', 'rare inborn error of glycerol kinase activity', 'glycerol kinase deficiency, X-linked recessive', 'GKD', 'inborn error of glycerol kinase activity', 'glycerol kinase deficiency', 'GK1 deficiency']",0060363,307030,308993,,"['-0.593', '0.1926', '-0.1813', '-0.05634', '0.0495', '-0.2257', '-0.2456', '0.1234', '-0.2374', '-0.05774', '-0.0894', '-0.0303', '0.1825', '0.03078', '-0.02832', '-0.0559', '-0.1173', '-0.04147', '-0.3228', '-0.6807', '0.2139', '-0.2266', '0.2257', '0.007545', '0.121', '-0.2554', '0.1311', '-0.1935', '-0.01865', '-0.2285', '0.3372', '0.2507', '0.2952', '0.2786', '-0.3108', '-0.2563', '0.03354', '-0.05258', '-0.01633', '-0.4387', '0.01339', '-0.3926', '0.2247', '-0.10645', '-0.2147', '-0.3538', '0.05927', '-0.0233', '0.253', '0.247', '-0.0945', '-0.1573', '0.1587', '0.001216', '0.1764', '-0.2157', '0.541', '-0.07935', '-0.274', '0.1716', '0.1362', '0.2227', '0.42', '-0.3286', '0.2067', '0.1312', '-0.00795', '-0.04858', '-0.3867', '-0.02963', '-0.3523', '0.01904', '-0.1726', '0.04993', '0.114', '0.03516', '0.1821', '0.06183', '-0.02385', '-0.2062', '0.1069', '0.23', '0.01779', '-0.10535', '0.1383', '0.1986', '0.1985', '0.12', '0.2979', '0.1724', '0.0457', '0.2462', '-0.2576', '-0.3452', '0.428', '0.6', '0.2113', '-0.6074', '-0.00551', '0.1315']",,,,,,,
mondo:0010614,X-linked congenital generalized hypertrichosis,"['congenital generalized hypertrichosis, Macias-Flores type', 'Macias-Flores Garcia-Cruz Rivera syndrome', 'hypertrichosis congenital generalised X-linked', 'hypertrichosis, congenital generalized', 'chromosome Xq27.1 interchromosomal insertion syndrome', 'hCG', 'congenital generalised hypertrichosis, Macias-Flores type', 'hypertrichosis, congenital generalized, X-linked dominant', 'chromosome Xq27.1 Interchromosomal insertion syndrome', 'hypertrichosis congenital generalized X-linked', 'Cgh', 'hypertrichosis, congenital generalised', 'HTC2', 'Macias Flores-Garcia Cruz-Rivera syndrome']",,307150,79495,,,,,C538388,,,,
mondo:0010615,isolated growth hormone deficiency type III,"['Growth hormone deficiency with hypogammaglobulinemia', 'isolated growth hormone deficiency type 3', 'X-linked hypogammaglobulinemia and isolated growth hormone deficiency', 'IGHD 3', 'X-linked isolated growth hormone deficiency', 'Fleisher syndrome', 'X-linked agammaglobulinemia and isolated growth hormone deficiency', 'isolated growth hormone deficiency, type IIi, with agammaglobulinemia, X-linked recessive', 'hypogammaglobulinemia and isolated Growth hormone deficiency, X-linked', 'X-linked IGHD', 'IGHD3', 'congenital isolated growth hormone deficiency type III', 'IGHD III', 'congenital isolated GH deficiency type III', 'isolated growth hormone deficiency, type III', 'growth hormone deficiency with hypogammaglobulinemia', 'isolated growth hormone deficiency, type 3', 'congenital IGHD type III', 'agammaglobulinemia and isolated Growth hormone deficiency, X-linked']",0060875,307200,231692,,"['-0.3442', '0.1423', '-0.2286', '-0.1675', '0.09344', '0.2269', '0.4438', '-0.11865', '-0.1288', '-0.2285', '0.015366', '-0.1453', '0.11597', '0.2401', '-0.3872', '-0.2808', '-0.04034', '-0.11926', '-0.1738', '-0.4194', '-0.0831', '-0.2086', '0.377', '-0.3645', '0.1437', '-0.11053', '0.0018835', '-0.016', '0.08167', '-0.2439', '0.12103', '-0.07043', '0.2766', '-0.1743', '-0.02571', '-0.159', '-0.05603', '0.02417', '-0.0681', '-0.1866', '0.03333', '0.2678', '0.0992', '-0.1265', '0.3464', '-0.2396', '0.1895', '-0.11273', '0.1274', '-0.0568', '0.1659', '-0.01912', '0.08295', '0.1814', '-0.1985', '0.1039', '0.3716', '-0.204', '-0.251', '0.1909', '0.0838', '0.1632', '-0.1449', '0.02196', '-0.1542', '0.3254', '0.3994', '0.3635', '-0.3386', '0.02068', '-0.199', '0.1705', '0.3892', '-0.2544', '0.012215', '0.2341', '0.1174', '0.02257', '-0.0588', '-0.1694', '-0.1915', '0.3682', '-0.1509', '0.001793', '-0.1545', '-0.1871', '0.3245', '-0.093', '0.3696', '0.03867', '0.1067', '0.004906', '0.01036', '-0.3057', '0.7964', '-0.015205', '0.1737', '-0.2715', '-0.1294', '0.3123']",,,C537149,,,,
mondo:0010617,male hypergonadotropic hypogonadism-intellectual disability-skeletal anomalies syndrome,"['hypogonadism, MALE, with mental retardation and skeletal anomalies', 'hypogonadism, MALE, with intellectual disability and skeletal anomalies', 'Sohval-Soffer syndrome']",,307500,2234,,,,,C564406,,,,
mondo:0010618,familial isolated hypoparathyroidism due to agenesis of parathyroid gland,"['HYPX', 'parathyroid glands, agenesis of', 'hypoparathyroidism, X-linked', 'X-linked hypoparathyroidism']",0111388,307700,2239,CN201292,"['-0.1702', '-0.2659', '-0.065', '-0.3394', '-0.6094', '0.7466', '-0.1881', '0.7046', '-1.102', '-0.9883', '-0.4695', '0.006874', '-0.5083', '1.029', '-0.3274', '0.7437', '0.3552', '-0.2001', '-0.639', '-0.627', '0.0805', '-0.3464', '-0.05322', '-0.3997', '0.1896', '-0.2803', '-0.1385', '-0.1406', '0.522', '-1.031', '-0.07947', '0.5137', '-0.2812', '-0.1495', '-0.2214', '-0.5317', '0.336', '0.0339', '0.842', '0.1802', '0.3005', '0.1473', '0.5', '-0.4778', '0.4229', '-0.824', '0.5615', '0.3418', '-0.1426', '0.4275', '-0.02266', '0.5083', '0.9536', '-0.01043', '-1.043', '-0.57', '-0.0154', '-0.6226', '-0.73', '-0.375', '0.0269', '-0.4072', '0.3894', '-0.318', '-0.7593', '0.8804', '0.4858', '1.077', '-0.736', '0.05884', '0.1537', '-0.0204', '0.182', '-0.3225', '0.2712', '0.383', '0.3936', '0.3064', '0.076', '0.632', '0.4185', '0.844', '-0.2266', '-0.7075', '0.0654', '-0.665', '-0.3901', '0.3298', '0.6187', '0.1276', '-0.1915', '0.7197', '-0.1638', '-0.264', '0.1573', '0.1171', '0.1875', '-0.9688', '-0.01637', '0.532']",C131079,,C563238,,,,
mondo:0010619,X-linked dominant hypophosphatemic rickets,"['hypophosphatemic rickets, X-linked dominant', 'hypophosphatemic rickets X-linked dominant', 'hypophosphatemia, vitamin D-resistant rickets', 'XLHR', 'hypophophatemic vitamin D-resistant rickets', 'vitamin D-resistant rickets, X-linked', 'X-linked hypophosphatemia', 'hypophosphatemic rickets, X-linked', 'hypophophatemia, X-linked', 'HYP', 'XLH', 'hypophosphatemic rickets, X-linked dominant, X-linked dominant', 'X-linked hypophosphatemic rickets', 'rickets, vitamin D-resistant', 'HPDR', 'hypophosphatemic vitamin D-resistant rickets', 'X-linked hereditary hypophosphatemic rickets', 'hereditary hypophosphatemic rickets, X-linked', 'hypophosphatemia, X-linked']",0050445,307800,89936,,"['0.3975', '-0.03918', '0.3699', '-0.2009', '-0.1436', '0.18', '-0.7827', '1.153', '-0.2479', '0.02118', '0.5923', '0.511', '-0.601', '0.838', '-0.6045', '-0.2332', '-0.1688', '0.1381', '-0.7935', '-0.7793', '-0.0571', '-1.146', '0.5835', '-0.2832', '0.2776', '-0.0938', '-0.002897', '-0.2812', '0.1997', '-0.1224', '0.0975', '-0.2015', '-0.5405', '0.07465', '0.1991', '-0.2357', '-0.05634', '0.08966', '0.6333', '0.2913', '-0.10205', '-0.1362', '-0.4504', '-0.10693', '0.1344', '-0.3943', '0.4229', '0.0157', '0.262', '0.4937', '-0.1569', '-1.031', '0.2365', '0.3257', '-0.6885', '-0.4019', '-0.1067', '0.0576', '-1.253', '0.2507', '0.6445', '-0.389', '-0.4624', '0.524', '0.4033', '0.7773', '0.8643', '1.2', '-0.484', '-0.546', '0.5146', '0.0976', '0.467', '-0.565', '0.03087', '1.285', '0.1564', '-0.8774', '0.4822', '0.4006', '0.2803', '0.297', '0.543', '0.03906', '-0.4885', '-0.05334', '0.3684', '0.1449', '0.7476', '0.402', '0.5713', '0.2256', '-0.648', '-0.1288', '-0.179', '0.2216', '0.7915', '-0.31', '-0.304', '-0.362']",C85234,,D053098,,E83.3,,
mondo:0010620,"hypouricemia, familial renal, due to tubular hypersecretion","['hypouricemia, familial renal, due to tubular hypersecretion']",,307830,,C1843972,,,,C564405,,,,
mondo:0010621,CHILD syndrome,"['CHILD syndrome, X-linked dominant', 'child syndrome', 'child nevus', 'ichthyosiform erythroderma, unilateral, with ipsilateral malformations, especially absence deformity of limbs', 'ichthyosis, child syndrome', 'congenital hemidysplasia with ichthyosiform nevus and limbs defects', 'congenital hemidysplasia with ichthyosiform erythroderma and limb defects', 'congenital hemidysplasia with ichthyosiform nevus and limb defects']",0111822,308050,139,C0265267,"['0.03537', '-0.1239', '-0.1155', '-0.545', '0.568', '-0.282', '-0.43', '0.1019', '-0.5835', '-1.096', '-0.004223', '-0.1274', '-0.539', '0.154', '-0.2903', '-0.1287', '-0.2883', '-0.3762', '0.1644', '-0.8433', '-0.00295', '0.1486', '0.1812', '-0.6577', '-0.3284', '-0.12445', '-0.3093', '0.3425', '0.529', '-0.0928', '0.3232', '-0.2382', '-0.12085', '0.11566', '0.1737', '0.0769', '0.1288', '-0.4993', '-0.2323', '0.504', '0.179', '-0.556', '0.3577', '-0.2042', '-0.1832', '0.1892', '-0.5693', '0.2144', '-0.1069', '0.2064', '-0.1063', '-0.1163', '0.7266', '0.3074', '-0.905', '0.3777', '0.3113', '0.0818', '0.04', '0.294', '-0.005653', '0.0913', '-0.4465', '0.3826', '-0.365', '-0.229', '0.491', '1.004', '-0.2903', '0.414', '0.1339', '-0.192', '-0.0984', '-0.10016', '0.1004', '0.3901', '-0.05472', '-0.02246', '-0.25', '-0.3196', '-0.3728', '0.4592', '0.1792', '0.535', '-0.456', '0.06616', '0.273', '0.2815', '0.00906', '-0.1761', '0.1769', '0.4338', '0.4834', '0.3164', '0.4836', '-0.4153', '0.3044', '0.09656', '0.2568', '0.3438']",,,C562515,759.89,,,
mondo:0010622,recessive X-linked ichthyosis,"['X-linked ichthyosis', 'RXLI', 'SSDD', 'ichthyosis, X-linked', 'steroid sulfatase deficiency disease', 'ichthyosis, X-linked, complicated', 'X-linked placental steryl-sulphatase deficiency', 'XLI', 'X-linked recessive ichthyosis', 'ichthyosis , X-linked, X-linked recessive', 'steroid sulfatase deficiency', 'STS deficiency', 'placental steroid sulfatase deficiency', 'X-linked ichthyosis with steryl-sulphatase deficiency', 'X linked ichthyosis', 'ichthyosis (disease), X-linked']",1700,308100,461,C0079588,"['0.334', '0.2098', '-0.0762', '-1.106', '0.704', '-0.4636', '0.11255', '-0.1262', '-0.07916', '-0.388', '-0.02934', '-0.02649', '-0.349', '-0.272', '0.00844', '-0.1852', '0.2637', '-0.348', '-0.1405', '-0.8545', '-0.4417', '0.1531', '0.2498', '-0.3096', '0.268', '0.4028', '-0.3608', '0.01569', '0.2069', '-0.3486', '0.3464', '-0.1337', '0.7935', '0.254', '0.2341', '-0.288', '-0.333', '-0.4763', '-0.513', '-0.458', '0.1462', '0.04202', '-0.0728', '0.3655', '0.3652', '-0.3997', '0.0896', '0.1475', '0.1288', '-0.1931', '0.1902', '-0.146', '0.1791', '-0.1849', '0.2074', '0.3616', '0.4045', '-0.1453', '-0.1816', '-0.3064', '0.0667', '-0.3674', '0.519', '0.2734', '0.3403', '0.1677', '0.1592', '0.4314', '-0.3025', '0.2351', '-0.8354', '0.04333', '0.1383', '-0.1036', '0.324', '-0.0787', '0.3894', '-0.1957', '0.09875', '-0.1913', '0.0815', '0.2042', '-0.2598', '0.09955', '-0.1495', '-0.3835', '0.3232', '0.09045', '0.10645', '-0.07605', '-0.07135', '0.3286', '0.6147', '0.3406', '0.865', '-0.06793', '-0.1514', '0.07275', '0.4583', '0.1512']",C84779,,,,,10048063,
mondo:0010623,ichthyosis and male hypogonadism,"['Ichthyosis-male hypogonadism syndrome', 'rud syndrome', 'ichthyosis and male hypogonadism', 'Ruds']",,308200,431,C1839989,,,,C537365,759.89,,,
mondo:0010625,"immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein","['immunodeficiency, X-linked, with deficiency of 115,000 Dalton surface glycoprotein', 'Gpl115 deficiency']",,308220,,C1839982,,,,C564120,,,,
mondo:0010626,hyper-IgM syndrome type 1,"['hyper-IgM immunodeficiency, X-linked', 'HIGM1', 'CD40 ligand deficiency', 'HIGMX-1', 'hyper-IgM syndrome type 1', 'hyper-IgM syndrome', 'hyper-IgM syndrome, X-linked', 'immunodeficiency, X-linked, with hyper-IgM, X-linked recessive', 'hyper IgM immunodeficiency, X-linked', 'hyper-IgM syndrome due to CD40 ligand deficiency', 'X-linked hyper IgM syndrome', 'X-linked hyper-IgM syndrome', 'XHIGM', 'immunodeficiency 3', 'HIGM', 'XHIM', 'hyper-IgM syndrome 1', 'hyper-IgM syndrome due to CD40L deficiency', 'hyper IgM syndrome 1', 'immunodeficiency with hyper IgM type 1', 'hyperimmunoglobulin M syndrome', 'IHIS', 'hyper IgM syndrome', 'immunodeficiency with hyper-IgM, type 1']",6620,308230,101088,C0398689,"['-0.256', '0.667', '-0.3142', '-0.2566', '0.0875', '-0.2211', '-0.523', '-0.164', '-0.0964', '-0.447', '0.0002264', '0.283', '0.416', '0.526', '0.3433', '-0.5234', '0.08026', '0.264', '0.06244', '-0.3923', '-0.2301', '-0.09', '0.719', '0.3306', '0.44', '-0.294', '-0.297', '-0.09314', '0.1584', '-0.04398', '0.4863', '-0.1691', '0.5117', '0.3206', '0.3823', '-0.438', '0.1515', '0.1159', '-0.1274', '-0.1886', '0.2827', '-0.2197', '0.0417', '-0.6187', '-0.5', '-0.6665', '0.1267', '-0.4727', '0.02155', '0.1236', '0.178', '-0.626', '-0.2588', '0.1008', '-0.4817', '0.304', '0.6006', '-0.04468', '-0.0861', '0.603', '-0.0282', '0.2184', '0.108', '0.3992', '0.4158', '-0.1359', '-0.1897', '0.3374', '-0.1272', '0.1384', '0.0427', '0.01747', '0.0288', '-0.2064', '0.2089', '0.3184', '-0.1824', '-0.02324', '-0.2683', '-0.01049', '0.0655', '0.1594', '0.2028', '-0.04233', '-0.531', '-0.3918', '0.2197', '-0.0167', '0.3037', '0.1655', '0.0994', '0.1531', '-0.2103', '-0.1782', '0.5156', '0.4153', '-0.3086', '-0.581', '-0.1577', '0.10297']",C61244,,,,,,
mondo:0010627,X-linked lymphoproliferative syndrome,"['SH2D1A-related lymphoproliferative disease, X-linked', 'X-linked lymphoproliferative syndrome 1', 'lymphoproliferative syndrome, X-linked, type 1', 'lymphoproliferative syndrome X-linked 1', 'X-linked lymphoproliferative syndrome type 1', 'Purtilo syndrome', 'XLP', 'XLP1', 'Duncan disease', 'lymphoproliferative syndrome, X-linked', 'lymphoproliferative syndrome, X-linked, 1', 'X-linked lymphoproliferative syndrome', 'X-linked lymphoproliferative disease']",0060705,,2442,C0549463,"['-0.12225', '0.2491', '0.0837', '-0.2129', '-0.04483', '-0.2861', '0.0309', '-0.105', '0.01643', '-0.2316', '0.09607', '0.02493', '-0.0546', '-0.1177', '0.0338', '-0.1558', '-0.0991', '0.0924', '-0.2181', '-0.381', '-0.0597', '-0.252', '0.2378', '-0.2988', '-0.0475', '-0.05725', '-0.1798', '-0.0982', '0.02068', '-0.445', '0.131', '0.2742', '0.2537', '-0.0784', '0.1276', '-0.0889', '-0.1732', '-0.1327', '-0.08746', '-0.1405', '-0.04425', '-0.1056', '0.0695', '-0.2412', '-0.1898', '-0.2905', '0.0377', '-0.01487', '0.1824', '0.213', '-0.1665', '0.05634', '-0.01888', '0.1416', '-0.3271', '0.04126', '0.1224', '-0.181', '-0.183', '0.02045', '0.224', '0.07654', '0.1703', '0.1456', '0.1807', '0.1548', '0.2664', '0.12415', '-0.27', '0.4434', '-0.2505', '-0.0179', '0.0551', '-0.05988', '0.26', '0.216', '0.1122', '0.02606', '0.0004582', '0.0399', '-0.2617', '-0.138', '-0.081', '0.1848', '0.02844', '-0.04968', '0.2844', '0.2164', '0.0175', '0.122', '0.2595', '0.1886', '0.11096', '0.05737', '0.4917', '0.3877', '0.2903', '-0.3296', '-0.12036', '-0.2578']",C61246,,,238.79,,10068348,
mondo:0010628,"immunoglobulin M, level of","['immunoglobulin M, level of']",,308250,,,,,,,,,,
mondo:0010629,"impacted teeth, multiple","['impacted teeth, multiple']",,308280,,,,,,,,,,
mondo:0010630,imprinting gene related to retinoblastoma,['imprinting gene related to retinoblastoma'],,308290,,,,,,,,,,
mondo:0010631,incontinentia pigmenti,"['incontinentia pigmenti, X-linked dominant', 'Bloch-Siemens syndrome', 'IP', 'IP2 (formerly)', 'Bloch-Sulzberger syndrome', 'Incontinentia pigmenti type 2 (formerly)', 'Incontinentia pigmenti, type II, formerly', 'Incontinentia pigmenti, type II', 'Incontinentia pigmenti syndrome', 'Incontinentia pigmenti, familial Male-lethal type', 'incontinentia pigmenti']",12305,308300,464,C0022283,"['1.025', '0.6235', '-0.1322', '-0.1334', '0.2546', '0.1378', '0.288', '0.4094', '-0.2273', '-0.1126', '-0.4524', '-0.2201', '0.04874', '0.3796', '-0.06537', '-0.1844', '0.2351', '-0.452', '-0.1892', '-0.7607', '-0.583', '-0.3315', '0.979', '-0.1525', '-0.919', '-0.02098', '-0.483', '-0.0604', '-0.3008', '-0.5703', '0.1066', '-0.421', '0.273', '-0.29', '-0.2905', '0.9097', '0.1427', '-0.2001', '-0.4404', '-0.7144', '0.251', '0.586', '0.3079', '0.2018', '0.3628', '-0.36', '-0.5317', '-0.3352', '-0.2179', '-0.2275', '-0.1561', '0.3254', '-0.5024', '-0.1743', '-0.765', '0.3638', '0.7646', '-0.4692', '-0.6675', '-0.01196', '0.477', '0.0808', '-0.1398', '0.854', '-0.04022', '0.2524', '0.3638', '0.4622', '0.1613', '0.2079', '-0.6006', '-0.2162', '-0.1989', '0.1068', '0.1855', '-0.2039', '-0.144', '-0.0359', '0.2236', '-0.2258', '-0.01593', '-0.11945', '-0.0493', '0.3547', '0.1864', '0.2896', '0.269', '0.012825', '0.10114', '0.586', '0.1334', '0.05478', '0.3787', '0.9883', '0.384', '-0.1613', '0.516', '-0.02965', '0.53', '0.467']",C84787,1000672,D007184,,,,
mondo:0010632,"developmental and epileptic encephalopathy, 1","['DEE1', 'early infantile epileptic encephalopathy caused by mutation in arx', 'infantile epileptic-dyskinetic encephalopathy', 'XMESID', 'EIEE1', 'infantile spasm syndrome, X-linked 1', 'ARX early infantile epileptic encephalopathy', 'Ohtahara syndrome, X-linked', 'epileptic encephalopathy, early infantile, 1', 'epileptic encephalopathy, early infantile, type 1', 'developmental and epileptic encephalopathy 1, X-linked recessive', 'West syndrome, X-linked']",0080468,308350,,C3463992,,,,,,,,
mondo:0010633,iris hypoplasia with glaucoma,"['iris hypoplasia with glaucoma', 'iris hypoplasia and glaucoma', 'IHG']",,308500,,C1839928,,,,C535538,,,,
mondo:0010634,"jaundice, familial obstructive, of infancy","['jaundice, familial obstructive, of infancy']",,308600,,C1839927,,,,C564118,,,,
mondo:0010635,hypogonadotropic hypogonadism 1 with or without anosmia,"['KMS', 'Kallmann syndrome, X-linked', 'HH1', 'KAL1', 'ANOS1 hypogonadotropic hypogonadism', 'Kallmann syndrome 1', 'hypogonadotropic hypogonadism 1 with or without anosmia (Kallmann syndrome 1), X-linked recessive', 'Kallmann syndrome, type 1, X-linked', 'hypogonadotropic hypogonadism and anosmia', 'anosmic hypogonadism', 'hypogonadotropic hypogonadism caused by mutation in ANOS1', 'hypogonadotropic hypogonadism 1 with or without anosmia', 'dysplasia olfactogenitalis of de Morsier', 'dysplasia Olfactogenitalis of De Morsier']",0090094,308700,,C1563719,,C75480,,,,E23.0,,
mondo:0010636,Kallmann syndrome with spastic paraplegia,"['spastic paraplegia-Kallmann syndrome', 'Kallmann syndrome with spastic paraplegia']",,308750,,C1839911,,,,C536873,,,,
mondo:0010637,"keratosis follicularis spinulosa decalvans, X-linked","['Kfsdx', 'keratosis follicularis spinulosa decalvans cum ophiasi', 'keratosis follicularis spinulosa decalvans, X-linked', 'KFSDX', 'keratosis follicularis SPINULOSA decalvans, X-linked', 'keratosis follicularis spinulosa decalvans', 'keratosis follicularis spinulosa decalvans, X-linked, X-linked recessive', 'keratosis follicularis Spinulosa decalvans cum Ophiasi']",0080754,308800,,C3887525,,,,C536159,,,,
mondo:0010638,keratosis follicularis-dwarfism-cerebral atrophy syndrome,"['dwarfism, cerebral atrophy and generalized keratosis follicularis', 'keratosis follicularis, dwarfism, and cerebral atrophy', 'keratosis follicularis dwarfism and cerebral atrophy', 'dwarfism, cerebral atrophy and generalised keratosis follicularis']",,308830,2339,C1839910,,,,C536158,,,,
mondo:0010639,laryngeal abductor paralysis-intellectual disability syndrome,"['laryngeal abductor paralysis', 'vocal cord dysfunction, familial', 'Plott syndrome']",,308850,2375,CN201604,,,,,,,,
mondo:0010640,"Leber optic atrophy, susceptibility to","['Leber hereditary optic neuropathy, modifier of', 'Lhon, modifier of', 'Loas', 'Leber optic atrophy, susceptibility to', 'Leber hereditary optic neuropathy, modifier of, X-linked dominant']",,308905,,,,,,,,,,
mondo:0010641,X-linked diffuse leiomyomatosis-Alport syndrome,"['Xq22.3 microdeletion syndrome', 'diffuse leiomyomatosis in Alport syndrome', 'leiomyomatosis, esophageal and vulval, with nephropathy', 'Alport syndrome with diffuse leiomyomatosis', 'Alport syndrome and diffuse leiomyomatosis', 'leiomyomatosis, diffuse, with Alport syndrome', 'DL-ATS', 'ATS-DL', 'chromosome Xq22.3 centromeric deletion syndrome']",,308940,1018,,,,,C537113,,,,
mondo:0010642,Lesch-Nyhan phenotype with normal HGPRT,['Lesch-Nyhan phenotype with normal HGPRT'],,308950,,,,,,,,,,
mondo:0010643,acute leukemia,"['stem cell leukaemia (disease)', 'stem cell leukaemia', 'acute leukemia', 'acute leukemia (disease)', 'stem cell leukemia', 'leukemia, acute, X-linked', 'acute leukaemia (disease)', 'stem cell leukemia (disease)']",12603,,,,,C9300,1000068,C564112,208.00,,,0002488
mondo:0010644,"proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis","['proteinuria, low molecular weight, with hypercalciuria and nephrocalcinosis', 'proteinuria, low molecular weight, with hypercalciuric nephrocalcinosis, X-linked recessive']",0111815,308990,93622,C1839874,,,,C545036,,,,
mondo:0010645,oculocerebrorenal syndrome,"['oculo-cerebro-renal syndrome', 'Lowe syndrome, X-linked recessive', 'phosphatidylinositol 4,5-bisphosphate 5-phosphatase deficiency', 'OCRL', 'Lowe disease', 'Lowe syndrome', 'Lowe oculocerebrorenal syndrome', 'OCR', 'oculocerebrorenal dystrophy', 'Ocrl1', 'oculocerebrorenal syndrome of Lowe', 'Lowe oculo-cerebro-renal syndrome', 'oculo-cerebro-renal dystrophy', 'phosphatidylinositol 4,5-biphosphate 5-phosphatase deficiency']",1056,309000,534,C0028860,"['0.1002', '0.1337', '0.8545', '-0.6284', '0.1825', '0.1128', '-0.743', '0.8384', '-0.6396', '0.12317', '0.2483', '0.11163', '0.313', '0.4531', '-0.1011', '-0.00875', '0.748', '-0.01381', '0.1589', '-0.615', '-0.1656', '-0.4583', '0.0445', '-0.1924', '-0.08105', '-1.149', '-0.2607', '-0.256', '0.11053', '-0.1813', '-0.4023', '-0.5254', '0.649', '0.3677', '-0.2932', '-0.4856', '-0.1967', '-0.4639', '-0.259', '-0.09894', '0.5176', '-0.04895', '0.5054', '0.0575', '0.293', '-0.2542', '0.02893', '-0.02069', '0.0757', '0.524', '-0.8384', '0.344', '0.37', '-0.561', '-0.3599', '-0.1881', '1.009', '-0.1538', '-0.7876', '0.003716', '0.1186', '-0.1274', '0.2239', '0.1018', '0.586', '-0.2952', '0.1517', '0.0856', '-0.04694', '-0.0259', '-0.2512', '-0.4517', '0.1711', '0.1748', '-0.04398', '-0.4697', '0.54', '-0.3247', '-0.2493', '0.1362', '-0.00775', '-0.2524', '-0.244', '0.4885', '-0.5923', '0.69', '0.524', '-0.1779', '0.389', '0.6475', '-0.0379', '0.6636', '-0.001514', '0.1927', '0.1455', '0.1683', '0.419', '0.04544', '0.4797', '0.6123']",C84940,,D009800,270.8,,10051707,
mondo:0010646,"macular dystrophy, X-linked","['macular dystrophy, X-linked']",,309100,,C1839842,,,,C564110,,,,
mondo:0010647,"spermatogenic failure, X-linked, 2","['azoospermia caused by mutation in TEX11', 'spermatogenic failure, X-linked, 2, X-linked recessive', 'TEX11 azoospermia', 'SPGFX2', 'Male infertility from defect in meiosis', 'spermatogenic failure, X-linked, type 2', 'spermatogenic failure, X-linked, 2']",0070185,309120,,C1839841,,,,,,,,
mondo:0010648,major affective disorder 2,"['MAFD2', 'major affective disorder 2', 'bipolar affective disorder', 'major affective disorder 2, X-linked dominant', 'manic-depressive psychosis, X-linked', 'manic-depressive illness', 'MAJOR affective disorder 2']",0080221,309200,,,,,,C564108,,,,
mondo:0010649,isolated congenital megalocornea,"['MGC1', 'congenital anterior megalophthalmia', 'megalocornea 1, X-linked, X-linked recessive', 'Mgcn', 'megalocornea']",,309300,91489,,"['-0.3962', '-0.1357', '-0.0628', '0.1211', '0.3125', '0.1438', '-0.004044', '0.5376', '-0.3845', '-0.1569', '-0.051', '-0.1469', '-0.1729', '0.0845', '-0.4854', '-0.47', '0.244', '-0.2059', '0.3335', '-0.7314', '-0.3472', '0.11224', '0.01309', '-0.1234', '0.3396', '0.04346', '-0.1284', '0.4326', '-0.0008335', '0.403', '0.2106', '0.2393', '0.2825', '0.2448', '-0.3901', '-0.02461', '-0.03394', '-0.3162', '0.06995', '-0.3513', '0.4785', '0.1665', '0.362', '-0.1049', '-0.10284', '0.2563', '0.0065', '0.188', '-0.04504', '-0.1919', '0.2874', '-0.0708', '-0.137', '-0.426', '-0.0411', '-0.144', '0.566', '-0.2278', '-0.3347', '-0.3994', '0.198', '0.02625', '-0.1758', '0.08484', '-0.2487', '-0.2778', '0.6035', '0.346', '-0.2375', '-0.0867', '0.1351', '0.4932', '0.354', '-0.446', '0.2008', '-0.3877', '0.2405', '-0.01024', '-0.323', '-0.102', '-0.3003', '0.139', '0.0784', '0.411', '-0.1377', '-0.2615', '0.1315', '0.1395', '0.1746', '0.0877', '0.3516', '0.6646', '-0.03275', '0.0983', '0.776', '-0.269', '0.2311', '-0.1702', '-0.1065', '0.1285']",,,,,,,
mondo:0010650,Melnick-Needles syndrome,"['MNS', 'osteodysplasty of Melnick and Needles', 'MELNICK-NEEDLES syndrome', 'Melnick-Needles syndrome, X-linked dominant', 'Melnick-Needles syndrome', 'Melnick-Needles osteodysplasty']",0111788,309350,2484,C0025237,"['-0.631', '0.2686', '0.3455', '-0.4795', '0.0751', '-0.51', '0.294', '0.9688', '-0.5967', '-0.2266', '-0.07', '-0.3794', '-0.2551', '-0.0337', '-0.08203', '0.06226', '0.3577', '0.5723', '-0.3064', '-0.0974', '-0.2427', '-0.12463', '0.4001', '-0.485', '-0.1232', '-0.4553', '-0.3484', '-0.0814', '0.7344', '-0.11774', '0.0352', '-0.3577', '0.1047', '0.3245', '0.06232', '-0.662', '0.3672', '-0.3245', '-0.1573', '-0.3386', '-0.565', '0.2761', '-0.09534', '0.1952', '-0.03168', '-0.08325', '-0.1522', '0.3733', '-0.566', '0.3486', '0.03168', '0.1098', '0.1065', '-0.04498', '-0.294', '-0.299', '-0.1567', '-0.2983', '0.1974', '0.02501', '0.3542', '0.3838', '-0.0611', '0.7065', '-0.015564', '-0.521', '0.0677', '0.4504', '-0.382', '0.4836', '-0.1764', '0.2642', '0.1482', '0.07135', '-0.3303', '-0.003258', '0.1637', '-0.005707', '-0.2311', '0.2222', '-0.239', '-0.3948', '0.544', '0.667', '-0.2444', '0.2485', '0.348', '0.05457', '0.4465', '0.06168', '-0.04767', '0.4294', '-0.0422', '0.3638', '0.7065', '0.1495', '0.566', '-0.7114', '0.475', '0.1826']",,,,756.59,,10060908,
mondo:0010651,Menkes disease,"['Menkes kinky hair syndrome', 'Trichopoliodystrophy', 'menkes disease, X-linked recessive', 'steely hair disease', 'MD', 'steely hair syndrome', 'MNK', 'Menkes disease', 'Menkes kinky-hair syndrome', 'kinky hair syndrome', 'Menkes syndrome', 'X-linked copper deficiency', 'kinky hair disease', 'Menkea syndrome', 'copper transport disease', 'Mk']",1838,309400,565,C0022716,"['-0.2485', '0.1046', '0.265', '-0.04507', '0.284', '-0.3984', '-0.509', '0.967', '-0.5225', '0.1826', '-0.523', '-0.285', '-0.2156', '0.08655', '0.1289', '-0.03577', '0.1803', '0.2944', '-0.8027', '-1.015', '0.03308', '-0.626', '0.7715', '-0.1472', '-0.1395', '-0.1487', '-0.0526', '-0.1339', '-0.1271', '-0.52', '0.8384', '0.03091', '-0.1937', '0.5156', '0.1748', '0.4058', '0.03333', '0.014915', '-0.06586', '0.41', '-0.2075', '-0.5747', '-0.2434', '0.3035', '0.2329', '-0.094', '0.1138', '0.01959', '0.06116', '0.1125', '-0.03708', '-0.06647', '-0.04227', '0.0314', '0.06793', '0.11993', '0.1746', '0.1831', '-0.15', '-0.2605', '0.0654', '0.2944', '-0.3167', '-0.376', '0.1649', '0.1067', '0.4092', '0.1154', '0.00765', '0.5435', '-0.11', '-0.0648', '0.05127', '0.10266', '-0.3677', '-0.1726', '0.4912', '-0.34', '-0.4626', '-0.5825', '-0.0743', '-0.854', '0.1176', '0.2316', '0.1818', '-0.01268', '-0.1355', '-0.3308', '0.1343', '-0.0585', '0.516', '0.09906', '0.527', '0.456', '0.2349', '0.2251', '0.3555', '0.001678', '0.3467', '-0.1343']",C75486,,D007706,759.89,,10027294,
mondo:0010652,X-linked intellectual disability-seizures-psoriasis syndrome,"['intellectual disability X-linked, Tranebjaerg type seizures and psoriasis', 'X-linked intellectual disability associated with psoriasis', 'Tranebjaerg-Svejgaard syndrome', 'mental retardation and psoriasis', 'intellectual disability and psoriasis', 'X-linked intellectual disability - seizures - psoriasis', 'mental retardation X-linked, Tranebjaerg type seizures and psoriasis', 'X-linked mental retardation associated with psoriasis', 'Tranebjaerg Svejgaard syndrome']",,309480,3052,,,,,C536978,,,,
mondo:0010653,Renpenning syndrome,"['X-linked intellectual disability with spastic diplegia', 'Sutherland-Haan X-linked mental retardation syndrome', 'mental retardation, X-linked 55', 'MRXS8', 'X-linked mental retardation syndromic 3', 'Renpenning syndrome type 1', 'renpenning syndrome, X-linked recessive', 'RENS1', 'X-linked intellectual disability, Renpenning type', 'MRXS3', 'intellectual disability, X-linked 55', 'mental retardation, X-linked, with spastic diplegia', 'intellectual disability, X-linked, syndromic 8', 'syndromic X-linked intellectual disability 8', 'mental retardation, X-linked, syndromic 3', 'X-linked intellectual disability syndromic 3', 'mental retardation, X-linked, Renpenning type', 'X-linked mental retardation Renpenning type', 'intellectual disability, X-linked, Renpenning type', 'Golabi-Ito-Hall syndrome', 'mental retardation, X-linked, syndromic 8', 'X-linked mental retardation with spastic diplegia', 'X-linked intellectual disability Renpenning type', 'syndromic X-linked mental retardation 8', 'intellectual disability, X-linked, syndromic 3', 'intellectual disability, X-linked, with spastic diplegia', 'intellectual disability, X-linked Renpenning type', 'Sutherland-Haan X-linked intellectual disability syndrome', 'X-linked intellectual disability due to PQBP1 mutations', 'mental retardation, X-linked Renpenning type', 'Sutherland-Haan syndrome', 'Renpenning syndrome 1']",0060179,309500,3242,C0796135,"['0.2439', '0.11584', '0.096', '-0.85', '0.1646', '-0.1873', '-0.05264', '0.8394', '-1.281', '-0.1912', '0.5464', '-0.1274', '0.3093', '-0.1136', '-0.07666', '-0.3623', '-0.01481', '-0.2218', '-0.4812', '-0.391', '-0.233', '0.2722', '0.3088', '0.2751', '0.3389', '-0.1292', '0.05377', '0.03683', '0.5947', '-0.08923', '0.2465', '-0.1395', '0.4937', '0.03973', '-0.3833', '-0.2253', '0.1178', '-0.5093', '0.00951', '-0.4062', '0.3364', '-0.4697', '0.0804', '-0.2686', '0.3726', '0.003504', '0.1807', '0.442', '0.1338', '0.2559', '-0.5024', '-0.2185', '-0.5635', '-0.155', '-0.1862', '-0.5513', '0.3958', '0.3638', '-0.1647', '0.7197', '-0.3203', '-0.1918', '-0.3804', '0.2563', '-0.2573', '-0.1846', '-0.3003', '0.5854', '-0.4875', '-0.1875', '-0.6235', '0.4602', '-0.02007', '0.01062', '0.263', '0.10876', '-0.03778', '-0.573', '-0.1936', '0.2224', '0.621', '0.1249', '-0.0959', '0.05518', '-0.1956', '0.00737', '0.05313', '-0.441', '0.1445', '0.3323', '-0.376', '0.431', '0.006645', '-0.01875', '0.6924', '0.1553', '0.2101', '-0.6973', '0.437', '0.1667']",C165533,,C537761,759.89,,,
mondo:0010654,Partington syndrome,"['intellectual disability, X-linked, syndromic 1', 'mental retardation, X-linked 36', 'MRXS1', 'Partington X-linked mental retardation syndrome', 'Partington-Mulley syndrome', 'Partington syndrome', 'mental retardation, X-linked, with dystonic movements, ataxia, and seizures', 'intellectual disability, X-linked, with dystonic movements, ataxia, and seizures', 'mental retardation, X-linked, syndromic 1', 'PRTS', 'Partington X-linked intellectual disability syndrome', 'X-linked Russell-Silver syndrome', 'intellectual disability-dystonic movements-ataxia-seizures syndrome', 'intellectual disability, X-linked 36', 'Partington syndrome, X-linked recessive', 'X-linked intellectual disability-dystonia-dysarthria syndrome']",14744,309510,94083,,"['-0.0808', '0.3186', '0.2595', '-0.563', '0.1128', '-0.7183', '0.0121', '0.3105', '-0.5996', '-0.568', '-0.3105', '0.2573', '0.085', '0.1359', '0.282', '0.4045', '0.006027', '-0.1471', '-0.32', '-0.5957', '-0.131', '0.1881', '-0.1831', '0.02042', '0.2302', '-0.1226', '-0.1476', '-0.0574', '0.3489', '-0.0644', '-0.2822', '-0.02135', '0.1802', '-0.3748', '0.1764', '-0.3232', '-0.5464', '-0.4844', '-0.2257', '-0.1172', '0.346', '-0.432', '-0.291', '-0.02454', '0.5283', '-0.236', '-0.375', '0.1963', '0.136', '-0.3801', '-0.2695', '0.4426', '-0.61', '-0.433', '0.3145', '-0.0795', '0.4763', '0.0669', '-0.06003', '0.333', '-0.0478', '0.2228', '0.657', '0.11554', '-0.4587', '0.0846', '0.01657', '0.001569', '-0.1697', '-0.07324', '-0.48', '0.0869', '0.0823', '0.2286', '0.4854', '0.575', '0.3909', '0.1714', '0.1993', '-0.11975', '0.2332', '-0.03162', '0.2422', '0.10315', '0.2952', '0.2369', '0.14', '0.7417', '0.403', '0.544', '0.0395', '0.3298', '0.05304', '0.0584', '0.8325', '0.695', '0.224', '-0.7217', '0.4001', '0.10394']",,,,,,,
mondo:0010655,X-linked intellectual disability with marfanoid habitus,"['intellectual disability, X-linked, with Marfanoid habitus', 'LUJAN-Fryns syndrome', 'Lujan syndrome', 'mental retardation, X-linked, with Marfanoid habitus', 'Marfanoid habitus, mild general hypotonia, hypernasal voice, normal testicular size and distinct craniofacial anomalies', 'Lujan-Fryns syndrome, X-linked recessive', 'Lujan-Fryns syndrome']",0080985,309520,776,,"['0.3306', '0.1907', '0.03162', '-0.535', '0.2274', '-0.4116', '-0.06134', '0.8564', '-0.9126', '-0.4849', '0.2302', '-0.006386', '0.331', '0.06015', '-0.137', '0.3088', '0.382', '-0.224', '-0.3792', '-0.7505', '-0.05228', '-0.1189', '0.3862', '-0.2632', '0.577', '-0.4062', '-0.1445', '0.009766', '0.4146', '-0.1365', '0.3347', '-0.308', '0.6914', '0.506', '0.03876', '-0.1003', '-0.2659', '-0.7', '0.00437', '-0.266', '0.4429', '-0.3538', '-0.0784', '0.10913', '0.6772', '-0.3262', '-0.0785', '0.2035', '0.3901', '0.07965', '-0.3298', '0.544', '-0.4795', '-0.1217', '0.131', '0.2072', '-0.5776', '-0.7573', '0.2482', '0.1713', '0.2299', '0.1167', '-0.1035', '0.5767', '-0.1132', '0.2847', '0.04288', '0.1497', '-0.0573', '0.6265', '-0.576', '0.003141', '-0.2039', '-0.0703', '-0.10834', '0.00965', '0.3176', '0.0718', '-0.2617', '-0.1373', '0.334', '-0.0447', '-0.2534', '0.1909', '0.0146', '0.393', '-0.5522', '-0.5645', '0.2795', '0.4053', '-0.2136', '0.3967', '-0.2803', '0.3884', '0.531', '-0.3916', '-0.1726', '-0.154', '0.598', '0.6343']",,,C537724,,,,
mondo:0010656,"intellectual disability, X-linked 1","['X-linked intellectual disability 78', 'MRX', 'mental retardation, X-linked 18', 'intellectual developmental disorder, X-linked 1, X-linked dominant', 'MRX1', 'mental retardation, X-linked type 1', 'mental retardation, X-linked 1', 'IQSEC2', 'IQSEC2-related epilepsy', 'X-linked intellectual disability 1/78', 'IQSEC2-related intellectual disability', 'MRX78', 'mental retardation, X-linked 78', 'X-linked intellectual disability 1']",0112038,309530,,,,C133729,,C567906,,,,
mondo:0010657,"methylmalonic acidemia with homocystinuria, type cblX","['methylmalonic acidemia and HOMOCYSTEINEMIA, cblX type', 'intellectual disability, X-linked 3', 'methylmalonic aciduria with homocystinuria, type cblX', 'methylmalonic aciduria and homocysteinemia, cblx type, X-linked recessive', 'mental retardation, X-linked 3', 'methylmalonic acidemia and homocysteinemia type cblX', 'combined defect in adenosylcobalamin and methylcobalamin synthesis, type cblX']",0111814,309541,369962,C0796208,"['-0.11707', '0.3257', '0.2319', '-0.1003', '0.169', '-0.2964', '-0.1686', '0.299', '-0.2659', '-0.1174', '-0.2712', '-0.02518', '0.1301', '-0.01651', '0.0796', '-0.1564', '0.1606', '-0.07367', '-0.097', '-0.3157', '-0.1693', '-0.129', '-0.01276', '-0.09314', '0.2277', '0.1199', '0.08295', '-0.2705', '0.0897', '-0.03029', '-0.10834', '0.1426', '0.1477', '0.0501', '-0.0873', '-0.004196', '-0.0752', '-0.3198', '-0.2201', '-0.1525', '0.06113', '-0.338', '0.02435', '-0.00951', '-0.10614', '-0.202', '0.06155', '0.1061', '-0.1099', '-0.0274', '-0.2009', '-0.02814', '-0.3804', '-0.1063', '-0.0751', '-0.0726', '0.05386', '-0.2117', '-0.1576', '0.3672', '0.2163', '-0.02606', '-0.11365', '-0.04092', '0.01414', '0.008514', '0.1559', '0.0856', '-0.2205', '0.1835', '-0.175', '0.1769', '0.03653', '-0.4258', '0.0791', '0.09064', '0.0535', '-0.2457', '-0.1982', '-0.0439', '0.1805', '-0.01024', '-0.2401', '0.2605', '0.1632', '0.176', '-0.1222', '0.1768', '0.4263', '0.2146', '0.0172', '0.1625', '-0.0392', '0.04462', '0.3652', '0.2913', '0.3643', '-0.329', '0.04413', '0.0879']",,,C563136,,,,
mondo:0010658,syndromic X-linked intellectual disability 12,"['X-linked intellectual disability, Wilson type', 'syndromic X-linked intellectual disability type 12', 'intellectual disability, X-linked, syndromic 12', 'mental retardation, X-linked, syndromic 12', 'MRXS12']",0060804,309545,85290,C1839792,,,,C564106,,,,
mondo:0010659,FRAXE intellectual disability,"['intellectual disability, X-linked, associated with fragile site FRAXE', 'fragile XE syndrome', 'FRAXE intellectual disability syndrome', 'FRAXE syndrome', 'intellectual disability associated with fragile site FRAXE', 'intellectual developmental disorder, X-linked 109, X-linked recessive', 'mental retardation, X-linked, associated with fragile site FRAXE', 'X-linked intellectual disability associated with fragile site FRAXE', 'X-linked mental retardation associated with fragile site FRAXE', 'fragile site, folic acid type', 'FRAXE mental retardation syndrome']",0080984,309548,100973,C0751157,"['-0.02637', '0.3677', '0.3513', '-0.3108', '0.0459', '-0.454', '0.1382', '0.504', '-0.3047', '-0.2668', '-0.1421', '-0.05914', '0.1177', '-0.09155', '0.374', '-0.1425', '0.074', '-0.09735', '-0.3462', '-0.4373', '-0.253', '0.3323', '0.2197', '-0.3472', '0.2954', '-0.2076', '-0.164', '-0.6655', '0.2893', '0.02092', '0.2345', '-0.2524', '0.3398', '0.335', '-0.2668', '-0.1451', '-0.4434', '-0.623', '-0.051', '-0.132', '0.4473', '-0.5825', '-0.1337', '-0.1815', '0.1498', '-0.3909', '0.1129', '-0.2158', '-0.06506', '0.1042', '-0.0774', '0.3494', '-0.6772', '-0.2705', '0.10516', '0.3638', '0.298', '-0.4553', '0.003052', '0.1957', '-0.0443', '0.05792', '0.2676', '0.444', '0.3352', '0.00895', '-0.2118', '-0.052', '-0.3599', '0.1317', '-0.1564', '0.1301', '-0.1919', '-0.539', '-0.01628', '0.7256', '0.3503', '-0.0996', '-0.544', '-0.279', '0.3584', '-0.3232', '-0.3743', '0.4626', '0.325', '0.31', '-0.08246', '0.3762', '0.2053', '0.2544', '0.1547', '0.3872', '-0.002132', '-0.07465', '0.5654', '0.2355', '0.393', '-0.478', '0.485', '0.0752']",,,,,,,
mondo:0010660,"intellectual disability, X-linked 9","['intellectual disability, X-linked 9', 'MRX9', 'intellectual developmental disorder, X-linked 9, X-linked recessive', 'intellectual disability, X-linked 44', 'mental retardation, X-linked 9', 'mental retardation, X-linked type 9', 'FTSJ1 non-syndromic X-linked intellectual disability', 'intellectual disability, X-linked type 9', 'non-syndromic X-linked intellectual disability caused by mutation in FTSJ1', 'mental retardation, X-linked 44']",0112034,309549,,C0796215,,,,C563137,,,,
mondo:0010661,"severe X-linked intellectual disability, Gustavson type","['gust', 'intellectual disability with optic atrophy, deafness, and seizures', 'intellectual disability X-linked severe Gustavson type', 'X-linked intellectual disability Gustavson type', 'Gustavson syndrome', 'mental retardation with optic atrophy, deafness, and seizures', 'X-linked mental retardation Gustavson type', 'mental retardation X-linked severe Gustavson type']",0081123,309555,3078,C0795965,,,,C536759,,,,
mondo:0010662,paraplegia-intellectual disability-hyperkeratosis syndrome,"['Fitzsimmons-McLachlan-Gilbert syndrome', 'mental retardation with spastic paraplegia and palmoplantar hyperkeratosis', 'intellectual disability with spastic paraplegia and palmoplantar hyperkeratosis']",,309560,2824,C2745996,,,,C537058,,,,
mondo:0010663,"intellectual disability-hypotonic facies syndrome, X-linked, 1","['Chudley mental retardation syndrome', 'Carpenter-Waziri syndrome', 'Chudley-Lowry-Hoar syndrome', 'mental retardation, X-linked, with growth retardation, deafness, and microgenitalism', 'intellectual disability Smith Fineman Myers type', 'intellectual disability, X-linked, with growth retardation, deafness, and microgenitalism', 'SFM1', 'X-linked intellectual disability-hypotonic face syndrome', 'Juberg-Marsidi syndrome', 'Juberg-Marsidi mental retardation syndrome', 'SFMS', 'mental retardation-hypotonic facies syndrome, X-linked, X-linked recessive', 'Juberg Marsidi syndrome', 'XLMR-hypotonic facies syndrome', 'MRXHF1', 'intellectual disability-hypotonic facies syndrome, X-linked, type 1', 'mental retardation-hypotonic facies syndrome, X-linked, type 1', 'X-linked hypogonadism gynecomastia intellectual disability', 'JMS', 'Chudley intellectual disability syndrome', 'mental retardation-hypotonic facies syndrome, X-linked, 1', 'Smith Fineman Myers syndrome 1', 'Chudley Lowry Hoar syndrome', 'Holmes-Gang syndrome', 'mental retardation-hypotonic facies syndrome X-linked, 1', 'mental retradation, X-linked with Growth delay, deafness, microgenitalism', 'intellectual disability-hypotonic facies syndrome, X-linked, 1', 'Smith-Fineman-Myers syndrome', 'Chudley syndrome 1', 'mental retardation Smith Fineman Myers type', 'Chudley-Lowry syndrome', 'intellectual disability-hypotonic facies syndrome X-linked, 1', 'X-linked hypogonadism gynecomastia mental retardation']",0080982,309580,93974,CN206718,"['-0.1838', '0.2029', '0.1671', '-0.3225', '-0.00135', '-0.3281', '0.0201', '0.1998', '-0.2698', '-0.235', '0.001909', '0.0488', '0.1837', '-0.1664', '-0.09357', '-0.0598', '0.1569', '0.1083', '-0.2876', '-0.3884', '0.1095', '0.1188', '0.2222', '-0.1715', '0.09186', '-0.007553', '-0.2057', '-0.1813', '0.2678', '-0.2452', '0.1188', '0.02756', '0.296', '0.10944', '-0.02394', '-0.12415', '-0.07184', '-0.3125', '-0.2101', '-0.3323', '0.00969', '-0.326', '-0.0696', '-0.1149', '0.01888', '-0.3633', '0.06555', '0.06915', '0.0492', '-0.1183', '-0.1345', '0.2173', '-0.09485', '-0.1984', '0.0121', '-0.3125', '0.1414', '-0.1697', '-0.341', '0.11646', '0.02829', '-0.0364', '0.02054', '0.1467', '0.156', '-0.0307', '0.2186', '0.1504', '-0.4062', '0.1274', '-0.4253', '0.004463', '0.174', '-0.1439', '0.0517', '0.161', '0.1323', '-0.04514', '-0.1874', '-0.001941', '0.2175', '0.0658', '-0.1965', '0.3652', '0.0311', '-0.02286', '0.10675', '0.4258', '0.2257', '0.0777', '0.3115', '0.2194', '0.0975', '0.05078', '0.3308', '0.2042', '0.1714', '-0.3882', '0.3296', '0.1816']",,,C537445,,,,
mondo:0010664,syndromic X-linked intellectual disability Snyder type,"['mental retardation, X-linked, syndromic, Snyder-Robinson type', 'intellectual disability, X-linked, Snyder-Robinson type', 'Snyder-Robinson intellectual disability syndrome', 'Snyder-Robinson syndrome', 'SRS', 'X-linked intellectual disability, Snyder type', 'intellectual developmental disorder, X-linked syndromic, Snyder-Robinson type, X-linked recessive', 'mental retardation, X-linked, Snyder-Robinson type', 'MRXSSR', 'spermine synthase deficiency', 'intellectual disability, X-linked, syndromic, Snyder-Robinson type', 'X-linked mental retardation Snyder-Robinson type', 'X-linked intellectual disability Snyder-Robinson type', 'Snyder-Robinson mental retardation syndrome']",0060802,309583,3063,C0796160,"['-0.2803', '-0.1671', '0.3767', '-0.5645', '-0.1967', '-0.4497', '-0.02426', '0.7324', '-0.6763', '-0.3225', '-0.3237', '-0.2157', '0.2368', '-0.12366', '-0.04346', '-0.07623', '0.683', '0.07227', '0.202', '-0.477', '0.4841', '0.1702', '0.2423', '-0.2483', '0.3196', '-0.000854', '0.12366', '-0.468', '0.07446', '-0.04547', '0.751', '-0.3784', '0.678', '0.02296', '0.05008', '-0.2834', '-0.5103', '-0.575', '-0.366', '-0.5854', '-0.3499', '-0.7954', '-0.6167', '0.2422', '0.1846', '-0.2472', '0.1991', '0.4136', '-0.2856', '0.2493', '-0.2917', '0.5044', '0.0991', '-0.03323', '-0.1749', '-0.532', '-0.0302', '-0.1664', '0.1335', '0.314', '-0.0813', '-0.3115', '-0.3909', '-0.2102', '-0.4915', '0.2136', '-0.05664', '0.3757', '-0.2225', '-0.0166', '-0.4985', '0.2095', '0.141', '-0.2727', '-0.1515', '0.2815', '-0.0417', '0.119', '-0.1232', '-0.06433', '-0.1952', '0.0442', '0.277', '0.525', '-0.1764', '0.4856', '-0.442', '0.2925', '0.463', '0.4114', '0.01221', '0.458', '0.0415', '0.5684', '0.5244', '0.551', '0.08136', '-0.02155', '0.4915', '0.1233']",,,C536678,758.89,,,
mondo:0010665,Wilson-Turner syndrome,"['mental retardation, X-linked, syndromic 6 (formerly)', 'mental retardation, X-linked, syndromic 6', 'Wilson-TURNER X-linked mental retardation syndrome', 'intellectual disability, X-linked, syndromic 6', 'MRXS6', 'Wilson-TURNER X-linked intellectual disability syndrome', 'mental retardation, X-linked, with gynecomastia and obesity (formerly)', 'X-linked intellectual disability-gynecomastia-obesity syndrome', 'Wilson-Turner syndrome, X-linked recessive', 'intellectual disability, X-linked, syndromic 6 (formerly)', 'WTS', 'intellectual disability, X-linked, with gynecomastia and obesity', 'Wilson Turner mental retardation syndrome (formerly)', 'X-linked intellectual disability - gynecomastia - obesity', 'intellectual disability, X-linked, with gynecomastia and obesity (formerly)', 'Wilson Turner intellectual disability syndrome (formerly)', 'mental retardation, X-linked, with gynecomastia and obesity']",0060814,309585,3459,,"['-0.3337', '-0.3687', '-0.0005755', '-0.0985', '0.1982', '-0.638', '-0.08185', '1.001', '-0.3438', '-0.742', '0.549', '-0.0812', '0.7036', '0.1608', '-0.1125', '-0.2183', '-0.1382', '0.523', '-0.523', '-0.3293', '-0.621', '0.1665', '0.2426', '-0.268', '0.4023', '-0.02661', '-0.2893', '0.3591', '0.6006', '-0.11383', '0.8105', '-0.4854', '0.5146', '0.05527', '-0.407', '-0.2766', '-0.11237', '0.2025', '0.1901', '-0.277', '0.5635', '0.3357', '0.2009', '-0.596', '0.0715', '-0.6567', '0.38', '0.1581', '-0.1316', '0.1365', '-0.3418', '0.1876', '-0.3506', '0.1232', '-0.1829', '-0.811', '-0.1181', '0.2908', '0.02992', '0.01328', '-0.3591', '-0.10016', '0.02574', '0.6265', '0.008095', '0.5073', '-0.06775', '0.583', '-0.2173', '0.4966', '0.3042', '-0.0619', '0.1343', '0.2266', '0.01994', '0.1089', '-0.2778', '0.137', '-0.125', '0.11346', '0.2776', '0.3208', '-0.1287', '-0.1328', '0.437', '-0.0063', '-0.05173', '0.363', '0.318', '0.4526', '-0.425', '0.612', '-0.346', '0.0651', '0.3757', '-0.0992', '-0.010414', '-0.444', '0.4243', '0.25']",,,C536708,,,,
mondo:0010667,Prieto syndrome,"['Prieto X-linked intellectual disability syndrome', 'intellectual disability, X-linked, with Dysmorphism and cerebral atrophy', 'mental retardation, X-linked, syndromic 2', 'mental retardation, X-linked, with Dysmorphism and cerebral atrophy', 'PRS', 'X-linked intellectual disability-dysmorphism-cerebral atrophy syndrome', 'Prieto X-linked mental retardation syndrome', 'Prieto-Badia-Mulas syndrome', 'intellectual disability, X-linked, syndromic 2', 'MRXS2', 'Prieto syndrome, X-linked recessive']",0060805,309610,2958,,,,,C535274,,,,
mondo:0010668,skeletal dysplasia-intellectual disability syndrome,"['Christian syndrome', 'mental retardation skeletal dysplasia abducens palsy', 'mental retardation-skeletal dysplasia', 'intellectual disability skeletal dysplasia abducens palsy', 'X-linked skeletal dysplasia-intellectual disability syndrome', 'intellectual disability, skeletal dysplasia, and abducens palsy', 'mental retardation, skeletal dysplasia, and abducens palsy', 'MRSD']",,309620,1436,C1839729,"['-0.483', '0.36', '0.42', '-0.4836', '0.1569', '-0.4375', '0.06525', '0.8374', '-0.2106', '-0.3413', '-0.0504', '-0.2444', '0.01011', '0.1377', '-0.406', '-0.000844', '0.134', '-0.3745', '-0.597', '-0.2515', '0.4006', '0.547', '0.4165', '-0.31', '0.0541', '-0.001126', '-0.10187', '-0.1278', '0.5586', '-0.669', '0.1161', '-0.8677', '0.06616', '-0.1127', '0.03065', '-0.288', '-0.1626', '-0.538', '-0.297', '-0.3098', '0.0429', '-0.1919', '0.4114', '0.002424', '0.09076', '-0.521', '0.02524', '-0.1349', '-0.827', '0.01819', '-0.2439', '-0.3953', '0.4312', '0.2168', '-0.1421', '-0.5156', '0.4224', '0.0893', '0.2266', '0.1422', '0.5728', '-0.374', '0.0444', '0.279', '-0.521', '-0.182', '-0.0909', '0.62', '-0.5312', '-0.008965', '-0.5107', '0.2356', '-0.1381', '-0.03708', '-0.3052', '0.371', '-0.1274', '-0.1663', '-0.2693', '0.02122', '-0.702', '0.466', '-0.12195', '0.4363', '0.255', '0.65', '0.08685', '0.08527', '0.491', '-0.1776', '-0.3022', '0.649', '0.2081', '-0.3225', '1.26', '-0.4392', '-0.0723', '-0.4656', '0.2932', '-0.292']",,,C564101,,,,
mondo:0010669,syndactyly type 8,"['non-syndromic syndactyly caused by mutation in FGF16', 'metacarpals 4 and 5 fusion', 'metacarpal 4-5 fusion', 'metacarpal 4-5 fusion, X-linked recessive', 'FGF16 non-syndromic syndactyly', 'fusion of metacarpals 4 and 5', 'MF4']",0111813,309630,2498,C1839728,"['0.01485', '-0.00206', '0.1708', '0.1483', '0.0887', '-0.2028', '0.02484', '0.1426', '-0.5986', '-0.7744', '0.08435', '0.2101', '-0.0927', '0.44', '-0.03204', '-0.3503', '0.529', '-0.27', '-0.1543', '-0.773', '-0.5176', '0.2917', '0.4976', '-0.2151', '0.6973', '0.0792', '-0.037', '0.3396', '-0.07166', '-0.195', '0.214', '-0.5894', '-0.09985', '0.3794', '0.4385', '-0.1495', '-0.0857', '-0.1287', '-0.1434', '-0.6743', '0.03534', '-0.5156', '0.1686', '-0.3801', '0.672', '-0.3914', '-0.01504', '0.215', '0.0662', '0.4624', '0.1852', '-0.08624', '0.1166', '-0.0354', '-0.3235', '-0.4497', '0.04184', '0.1364', '-0.1204', '0.06128', '0.647', '-0.1659', '-0.1252', '0.3835', '-0.2078', '-0.10095', '0.3198', '0.242', '-0.3167', '0.012825', '-0.4531', '0.2367', '0.6523', '-0.4436', '0.2893', '-0.0362', '-0.2454', '0.1241', '-0.4607', '-0.6313', '-0.1058', '-0.2988', '0.7754', '0.393', '0.2473', '-0.4236', '-0.9136', '-0.0784', '0.3086', '-0.6924', '-0.10925', '0.2708', '-0.188', '-0.1836', '0.253', '-0.02391', '0.4348', '-0.8438', '0.416', '0.39']",,,C564100,,,,
mondo:0010670,X-linked intellectual disability-spastic quadriparesis syndrome,"['intellectual disability with spastic paraplegia', 'mental retardation with spastic paraplegia']",,309640,163982,C1839727,,,,C564099,,,,
mondo:0010671,"microphthalmia, syndromic 1","['ANOP1, formerly', 'MCOPS4', 'microphthalmia syndromic 4', 'MAA, formerly', 'microphthalmia with ankyloblepharon and mental retardation', 'microphthalmia, syndromic type 1', 'microphthalmia, syndromic 4, formerly', 'syndromic microphthalmia type 4', 'microphthalmia, syndromic 1', 'MCOPS1', 'MCOPS4, formerly', 'microphthalmia with ankyloblepharon and intellectual disability', 'Lenz dysplasia', 'Lenz microphthalmia syndrome']",0111799,309800,85275,,,,,C564457,759.89,,,
mondo:0010672,linear skin defects with multiple congenital anomalies,"['microphthalmia dermal aplasia and sclerocornea syndrome', 'linear skin defects with multiple congenital anomalies', 'syndromic microphthalmia type 7', 'linear skin defects with multiple congenital anomalies type 1', 'MCOPS7', 'microphthalmia-dermal aplasia-sclerocornea syndrome', 'linear skin defects with multiple congenital anomalies 1', 'LSDMCA1', 'MIDAS syndrome', 'Micropthalmia syndromic 7', 'MLS syndrome', 'microphthalmia with linear skin defects syndrome']",0111875,,2556,,"['0.3044', '0.309', '0.09937', '-0.639', '0.3745', '-0.347', '-0.316', '-0.1681', '-0.514', '-0.813', '-0.006054', '-0.5835', '-0.0742', '0.2576', '-0.1242', '0.381', '-0.1137', '-0.3516', '-0.2815', '-0.6787', '-0.3125', '0.2299', '0.0788', '0.00415', '-0.0643', '-0.1348', '-0.5693', '0.1752', '0.2632', '0.4062', '0.619', '-0.3127', '-0.04956', '-0.817', '0.141', '0.415', '-0.1788', '-0.2988', '-0.06885', '-0.412', '0.3215', '0.3337', '0.1722', '-0.011345', '0.8857', '-0.299', '-0.1857', '-0.188', '0.2272', '-0.3684', '0.2375', '0.3464', '-0.1528', '0.2756', '-0.539', '0.1079', '0.03796', '0.415', '-0.4834', '0.311', '-0.3625', '-0.293', '0.2057', '0.4607', '-0.1707', '0.332', '0.2664', '0.6367', '-0.8037', '0.4082', '-0.646', '-0.1879', '-0.1603', '0.37', '0.1184', '0.0172', '0.05872', '-0.4797', '0.1237', '-0.09705', '0.07635', '0.3767', '0.0835', '0.1754', '-0.338', '-0.2308', '0.0858', '0.463', '0.449', '0.774', '-0.4263', '0.3628', '-0.034', '0.1433', '1.01', '-0.0754', '0.0463', '-0.1586', '0.4412', '-0.10175']",,,C537466,,,,
mondo:0010673,"modifier, X-linked, for Neurofunctional defects","['Tourette syndrome, modifier of', 'modifier, X-linked, for Neurofunctional defects']",,309840,,C1839708,,,,C564098,,,,
mondo:0010674,mucopolysaccharidosis type 2,"['IDS deficiency', 'MPS II - Hunter syndrome', 'mucopolysaccharidosis with skin involvement', 'mucopolysaccharidosis II', 'mucopolysaccharidosis type II', 'attenuated MPS (subtype; formerly known as mild MPS II)', 'MPSII', 'MPS with skin involvement', 'SIDS deficiency', 'Hunter syndrome', 'MPS II', 'sulfoiduronate sulfatase deficiency', 'severe MPS II', 'Hunter^s syndrome', 'deficiency of iduronate-2-sulphatase', 'MPS 2', 'iduronate 2-sulfatase deficiency', 'mucopolysaccharidosis, type 2', 'mucopolysaccharidosis, MPS-II', 'mucopolysaccharidosis, type II', 'MPS2', 'mucopolysaccharidosis II, X-linked recessive', 'I2S deficiency']",12799,309900,79388,C0026705,"['0.2527', '0.6323', '0.1863', '-0.133', '0.2142', '0.01622', '0.09155', '1.068', '-0.2769', '-0.01913', '0.091', '0.2153', '-0.2644', '0.6255', '-0.31', '-0.5176', '-0.2235', '-0.6626', '-0.5815', '-0.544', '0.6714', '-0.4624', '1.094', '-0.2313', '0.1309', '-0.5034', '0.4092', '0.341', '0.1768', '0.369', '0.9487', '0.4172', '0.2607', '-0.4004', '-0.3154', '0.06204', '-0.3003', '-0.8223', '0.4858', '-0.2666', '-0.0841', '-0.569', '0.79', '0.3528', '-0.4053', '0.07104', '0.1821', '-0.02782', '-0.58', '-0.2556', '-0.4377', '0.2076', '-0.1721', '-0.3823', '0.5723', '-0.233', '-0.000336', '-0.0589', '0.3188', '0.2164', '0.11346', '-0.1943', '-0.3665', '0.06046', '0.3384', '-0.701', '0.6313', '-0.1827', '-0.1809', '0.1931', '-0.2588', '-0.1855', '0.1024', '-0.2316', '0.0161', '-0.2081', '-0.05157', '0.0914', '-0.4116', '-0.7354', '-0.2234', '-0.787', '0.007248', '0.448', '-0.2234', '0.2075', '0.3003', '0.1708', '0.1449', '-0.006985', '-0.04816', '0.3372', '0.1852', '0.4258', '0.4392', '0.404', '-0.2286', '-0.3457', '1.055', '0.0766']",C61260,,D016532,,E76.1,10056889,
mondo:0010675,"muscular dystrophy, cardiac type","['muscular dystrophy, cardiac type']",,309930,,C1442927,,,,C563247,,,,
mondo:0010676,"muscular dystrophy, Hemizygous lethal type","['muscular dystrophy, Hemizygous lethal type']",,309950,,C1839671,,,,C564097,,,,
mondo:0010677,"muscular dystrophy, Mabry type","['muscular dystrophy, Mabry type']",,310000,,C1839670,,,,C564096,,,,
mondo:0010678,"muscular dystrophy, progressive Pectorodorsal","['muscular dystrophy, progressive, involving shoulder girdle and back', 'muscular dystrophy, progressive Pectorodorsal']",,310095,,C1839669,,,,C564095,,,,
mondo:0010679,Duchenne muscular dystrophy,"['severe dystrophinopathy, Duchenne type', 'muscular dystrophy, Duchenne', 'muscular dystrophy, pseudohypertrophic progressive, Duchenne type', 'DMD', 'Duchenne muscular dystrophy, X-linked recessive', 'Duchenne muscular dystrophy', 'muscular dystrophy, Duchenne type']",11723,310200,98896,C0013264,"['0.3328', '-0.4897', '-0.3997', '0.04175', '0.4897', '-0.5864', '0.6787', '1.07', '-1.571', '-0.537', '-0.10956', '0.396', '-0.0872', '0.6694', '0.2026', '0.12256', '-0.871', '-0.4365', '-0.4563', '-0.7334', '0.163', '-0.1743', '0.423', '0.287', '0.1573', '-0.548', '0.117', '-0.8784', '0.04544', '-0.278', '0.597', '0.1906', '0.9766', '0.3086', '-0.0811', '-0.1873', '-0.2761', '0.0532', '-0.2686', '-0.01918', '0.2637', '0.08624', '0.04172', '-0.11285', '0.00771', '0.711', '-0.10785', '0.4658', '-0.05295', '0.4668', '0.02403', '-0.1122', '0.1388', '-0.4968', '0.1957', '-0.2166', '0.0794', '0.8755', '-0.623', '-0.0817', '0.10504', '0.1912', '-0.1709', '0.1118', '0.1592', '-0.1439', '-0.03', '0.1322', '-0.2915', '-0.4', '0.00568', '-0.1654', '-0.3135', '-0.1838', '0.7754', '0.2075', '-0.1707', '-0.07574', '-0.2228', '0.151', '0.442', '-0.2712', '-0.4062', '0.3203', '-0.3733', '0.388', '-0.0192', '-0.4316', '0.6006', '0.4412', '-0.4226', '0.02892', '-0.04', '0.3813', '-0.1871', '-0.02832', '0.451', '-0.47', '-0.1589', '0.4102']",C75482,,D020388,,,10013801,
mondo:0010680,X-linked Emery-Dreifuss muscular dystrophy,"['humeroperoneal neuromuscular disease', 'EDMD1', 'muscular dystrophy, tardive, Dreifuss-Emery type, with contractures', 'Ehlers-Danlos syndrome, classic-like, 1', 'EMD1', 'Humeroperoneal neuromuscular disease, formerly', 'muscular dystrophy, tardive Emery-Dreifuss type, with contractures', 'EMERY-Dreifuss muscular dystrophy 1, X-linked', 'Humeroperoneal neuromuscular disease', 'scapuloperoneal syndrome, X-linked', 'Emery-Dreifuss muscular dystrophy, X-linked', 'Emery-Dreifuss muscular dystrophy 1, X-linked', 'Emerinopathy', 'scapuloperoneal syndrome, X-linked, formerly']",0070246,310300,98863,CN069573,"['-0.1703', '-0.6875', '-0.479', '-0.2842', '0.6875', '-1.391', '0.0736', '0.5854', '-1.944', '-1.014', '0.354', '0.367', '-0.1752', '1.1455', '0.4316', '0.3088', '-0.748', '-0.4087', '-0.717', '-0.5474', '-0.0397', '0.2183', '0.3071', '0.6416', '0.2173', '-0.2935', '0.01077', '-0.884', '0.3782', '-0.3862', '0.9995', '-0.05505', '0.534', '0.0667', '0.2595', '0.194', '-0.6187', '0.3694', '0.1898', '-0.6777', '0.0991', '-0.4783', '-0.3938', '0.4111', '-0.1935', '0.3533', '-0.00453', '0.661', '0.1041', '0.6465', '0.2986', '-0.4146', '0.173', '-0.7476', '0.3516', '-0.63', '0.657', '1.1455', '-0.2654', '0.03687', '0.007812', '0.02266', '-0.0475', '-0.0629', '0.05753', '0.11664', '0.02063', '0.647', '-0.497', '-0.1525', '-0.3333', '0.4023', '0.276', '-0.219', '0.7773', '0.5654', '0.001673', '0.3047', '0.1246', '0.2024', '0.2274', '-0.10455', '-0.3635', '0.2026', '-0.2634', '0.1504', '-0.1476', '-0.297', '1.042', '0.3184', '-0.4856', '0.1736', '0.3704', '0.926', '-0.1417', '0.0769', '0.2754', '-0.496', '-0.1824', '-0.0988']",C168730,,D000083143,,,,
mondo:0010681,myelolymphatic insufficiency,"['Myelolymphatic insufficiency', 'Pelger-like anomaly with leukopenia and susceptibility to infections']",,310350,,C1839650,,,,,,,,
mondo:0010683,X-linked centronuclear myopathy,"['X-linked myotubular myopathy', 'XLMTM', 'XLCNM', 'myopathy, centronuclear, X-linked', 'myotubular myopathy, X-linked', 'myotubular myopathy, X-linked, X-linked recessive', 'CNMX', 'MTM', 'myotubular myopathy 1', 'centronuclear myopathy, X-linked']",0111225,310400,596,C0410203,"['-0.7856', '-0.2766', '-1.213', '-0.686', '0.476', '-0.745', '-0.0586', '0.945', '-1.0', '-0.083', '-0.05765', '-0.2256', '0.275', '0.1783', '-0.11707', '0.3713', '0.00643', '0.08', '-0.3506', '-0.9575', '-0.0699', '-0.04214', '1.053', '-0.02194', '0.032', '-0.662', '-0.094', '0.2042', '-0.0451', '0.1548', '0.541', '-0.11896', '0.3467', '-0.1775', '-0.387', '-0.1713', '-0.466', '-0.5054', '0.4531', '-0.064', '-0.4446', '0.07776', '-0.1627', '0.4373', '0.1437', '0.04462', '-0.6284', '-0.2006', '-0.00897', '0.596', '-0.4407', '-0.6777', '-0.08026', '-0.1201', '0.0682', '-0.0848', '0.5093', '0.427', '-0.0739', '-0.2333', '0.192', '0.02637', '0.3796', '0.02731', '-0.2524', '0.04016', '0.3037', '0.8306', '-0.9673', '0.11584', '-0.4858', '0.05234', '-0.0582', '0.678', '0.00679', '-0.4192', '0.2578', '-0.01761', '-0.1256', '-0.1775', '-0.12164', '0.2076', '-0.365', '0.2101', '-0.4067', '0.4553', '0.184', '0.3655', '-0.2695', '-0.4219', '0.1362', '0.03073', '0.3005', '0.373', '0.6235', '-0.096', '0.5273', '0.02658', '0.4724', '0.04626']",C118781,,,,,,
mondo:0010684,X-linked myopathy with excessive autophagy,"['MEAX', 'XMEA', 'vacuolar myopathy', 'myopathy, X-linked, with excessive autophagy', 'myopathy, X-linked, with excessive autophagy, X-linked recessive']",0050760,310440,25980,C2931230,"['-0.2286', '0.4792', '-0.2488', '-0.3987', '0.04584', '-0.815', '-0.3457', '1.057', '-0.7383', '-0.11426', '-0.2031', '0.693', '0.11017', '0.408', '0.606', '0.596', '0.09467', '0.04364', '-0.1561', '-0.61', '-0.2426', '-0.1327', '0.05545', '-0.3833', '0.11255', '-0.3027', '0.2086', '0.0484', '-0.2242', '-0.2754', '0.603', '-0.1121', '0.3274', '-0.1842', '-0.0843', '-0.4307', '-0.192', '-0.439', '-0.2693', '-0.372', '-0.00531', '-0.36', '-0.3137', '-0.06085', '0.1394', '0.0881', '0.08563', '0.2346', '-0.2507', '0.02559', '0.03387', '-0.04242', '-0.1203', '-0.06216', '0.4146', '-0.561', '0.8076', '0.1965', '0.1809', '0.01706', '0.0817', '0.1874', '-0.02316', '-0.08105', '0.1682', '-0.29', '0.1576', '0.382', '-0.3992', '-0.1472', '-0.541', '-0.1819', '-0.0737', '0.10803', '0.932', '0.2418', '-0.3833', '-0.0355', '0.4246', '0.0627', '0.748', '-0.27', '0.7344', '0.503', '0.11005', '0.4524', '-0.01959', '0.0759', '0.4207', '0.1129', '-0.008514', '0.569', '-0.03763', '0.3398', '0.5757', '0.3093', '0.001957', '-0.448', '-0.1796', '-0.534']",,,C536522,,,,
mondo:0010685,"myopia 1, X-linked","['myopia 1, X-linked', 'myopia-1, X-linked recessive', 'MYP1']",,310460,,C1839612,,,,C564091,,,,
mondo:0010686,N syndrome,"['mental retardation, malformations, chromosome breakage, and development of T-cell leukemia', 'NSX', 'intellectual disability, malformations, chromosome breakage, and development of T-cell leukemia', 'intellectual disability, malformations, chromosome breakage, and development of T-cell leukaemia', 'mental retardation, malformations, chromosome breakage, and development of T-cell leukaemia', 'N syndrome']",0050769,310465,2608,C2936859,,,,C536108,,,,
mondo:0010687,"nephrolithiasis, X-linked recessive, with renal failure","['urolithiasis, X-linked recessive, type 1', 'nephrolithiasis, X-linked recessive, with renal failure', 'XRN', 'nephrolithiasis, type i, X-linked recessive', 'nephrolithiasis, X-linked recessive, type 1', 'nephrolithiasis 1']",,310468,93622,,"['-0.01712', '-0.3918', '-0.0781', '-0.1927', '-0.1033', '-0.34', '-0.2128', '0.516', '-0.4934', '0.303', '0.1328', '-0.3218', '-0.0969', '0.4792', '0.1494', '-0.3596', '-0.2122', '-0.07007', '0.4817', '-0.487', '0.6084', '-0.673', '0.5005', '-0.1338', '0.3916', '0.00887', '-0.1492', '-0.4797', '-0.0262', '0.1516', '0.4968', '-0.7354', '0.01257', '-0.1636', '-0.2954', '-1.14', '-0.2163', '-0.03702', '0.02505', '0.1177', '-0.0987', '-0.2363', '0.685', '-0.4038', '0.063', '-0.586', '-0.2397', '-0.2296', '-0.218', '0.263', '-0.1026', '0.676', '0.4487', '-0.317', '-0.0386', '-0.03488', '0.4814', '-0.3503', '-0.4631', '0.3542', '0.4138', '0.1672', '-0.01182', '-0.6143', '0.583', '0.221', '-0.1171', '0.4265', '0.0968', '0.3518', '0.1328', '-0.0996', '0.1228', '0.1816', '0.5576', '0.3267', '0.00515', '-0.606', '0.02235', '0.4805', '0.4053', '-0.2695', '0.4207', '0.004097', '-0.2664', '0.2957', '0.2206', '0.06146', '0.702', '0.1476', '0.1862', '-0.12244', '-0.1956', '-0.00767', '0.651', '0.3918', '0.6353', '-0.2544', '-0.03226', '0.1969']",,,C562901,,,,
mondo:0010688,hereditary sensory neuropathy X-linked,"['neuropathy, hereditary sensory, X-linked']",0070159,310470,,C1839602,,,,C564090,,,,
mondo:0010689,Charcot-Marie-Tooth disease X-linked recessive 4,"['CMTX4', 'Charcot-Marie-Tooth disease, X-linked recessive, 4', 'CMT4X', 'axonal motor sensory neuropathy with deafness and intellectual disability', 'CMTX 4', 'Cowchock syndrome, X-linked recessive', 'X-linked Charcot-Marie-Tooth disease type 4', 'NADMR', 'axonal motor sensory neuropathy with deafness and mental retardation', 'Charcot-Marie-Tooth disease X-linked recessive type 4', 'neuropathy, axonal motor-sensory, with deafness and intellectual disability', 'neuropathy, axonal motor-sensory with deafness and intellectual disability', 'COWCK', 'Charcot-Marie-Tooth disease with deafness and mental retardation', 'NAMSD', 'cowchock syndrome', 'neuropathy, axonal motor-sensory with deafness and mental retardation', 'neuropathy, axonal motor-sensory, with deafness and mental retardation', 'Charcot-Marie-Tooth disease with deafness and intellectual disability']",0110212,310490,101078,,"['0.2115', '0.2595', '0.223', '-0.01456', '0.2108', '-0.4238', '-0.08875', '0.772', '-0.57', '-0.3494', '0.03488', '0.4482', '-0.3555', '0.6025', '-0.1332', '-0.2646', '-0.2445', '-0.2091', '-0.8164', '-0.2856', '0.04498', '0.3442', '0.1901', '0.445', '0.1677', '0.3015', '0.11475', '-0.02008', '0.2969', '-0.0943', '0.3286', '-0.6', '0.1389', '0.248', '0.08234', '-0.678', '-0.668', '-0.2742', '0.3044', '-0.1071', '-1.134', '-0.4863', '-0.524', '0.3723', '-0.2175', '-0.1803', '-0.0362', '0.0212', '-0.1129', '0.0095', '-0.272', '0.1643', '-0.09174', '-1.166', '0.3882', '-0.09985', '0.01468', '0.2347', '-0.4414', '-0.1553', '-0.4536', '0.304', '0.669', '0.686', '-0.538', '1.174', '-0.4067', '0.872', '-0.656', '0.3027', '-0.9146', '0.1995', '0.3901', '-0.3403', '0.9336', '0.2527', '-0.4001', '0.554', '0.0922', '-0.4072', '0.02234', '0.0717', '0.7397', '0.5566', '0.2915', '-0.00863', '0.1313', '0.6626', '0.8955', '0.5264', '0.2052', '0.2458', '-0.1008', '0.547', '0.3357', '0.4824', '0.3643', '-0.6416', '0.02675', '0.3923']",,,,,,,
mondo:0010690,congenital stationary night blindness 1A,"['congenital stationary night blindness 1A X-linked', 'night blindness, congenital stationary, type 1A', 'NYX-related congenital stationary night blindness', 'congenital stationary night blindness caused by mutation in NYX', 'congenital stationary night blindness with myopia', 'nyctalopia', 'night blindness, congenital stationary (complete), 1A, X-linked, X-linked recessive', 'congenital stationary night blindness type 1A', 'CSNB1A', 'myopia-night blindness', 'CSNB, complete, X-linked', 'NYX congenital stationary night blindness', 'night blindness, congenital stationary, with myopia', 'NBMI', 'complete CSNB X-linked', 'hemeralopia-myopia']",0110870,310500,,,,,,,,,,
mondo:0010691,Norrie disease,"['Anderson-Warburg syndrome', 'Norrie-Warburg disease', 'atrophia bulborum hereditaria', 'Norrie-Warburg syndrome', 'nd', 'pseudoglioma', 'foetal iritis syndrome', 'Episkopi blindness', 'fetal iritis syndrome', 'ND', 'Norrie syndrome', 'NDP', 'Norrie disease, X-linked recessive', 'Norrie disease']",0060844,310600,649,,"['-0.11993', '-0.12225', '0.04083', '-0.1864', '0.585', '-0.0542', '-0.203', '0.968', '-0.3704', '-0.2595', '0.397', '-0.8877', '0.3845', '0.5664', '-0.2722', '-0.1076', '-0.217', '-0.04852', '0.1436', '-0.853', '-0.05338', '0.0719', '-0.3518', '-0.4788', '0.10004', '-0.05417', '-0.6772', '0.35', '0.3308', '0.516', '0.7925', '-0.04718', '0.2136', '0.602', '-0.6636', '0.05963', '-0.2812', '-0.624', '-0.2632', '-0.2908', '0.315', '0.1674', '0.3901', '0.1171', '-0.03375', '-0.04593', '-0.142', '-0.5664', '0.2227', '0.3274', '-0.2228', '0.1798', '-0.217', '-0.3005', '0.2822', '0.07196', '0.4766', '-0.04108', '-0.2448', '0.2175', '0.3035', '-0.1582', '0.2695', '0.5264', '-0.2488', '-0.1667', '0.252', '0.8604', '-0.0735', '0.4956', '0.1357', '0.1647', '-0.2935', '-0.05118', '0.4949', '-0.1355', '0.1512', '0.11884', '-0.8315', '-0.09546', '0.1215', '-0.1907', '0.101', '0.64', '0.0266', '0.0958', '0.0839', '0.4602', '-0.02237', '0.8306', '0.4863', '0.812', '-0.2113', '0.2223', '0.6826', '-0.4873', '0.481', '0.1265', '0.537', '0.04703']",C118634,,C537849,743.8,H35.5,10069760,
mondo:0010692,nuclear ribonucleic acid,"['nRNA', 'nuclear ribonucleic acid']",,310650,,,,,,,,,,
mondo:0010693,"nystagmus 1, congenital, X-linked","['NYSTAGMUS 1, congenital, X-linked', 'Nystagmus 1, infantile, X-linked', 'Nystagmus 1, congenital, X- linked', 'Nystagmus, infantile idiopathic', 'congenital nystagmus caused by mutation in FRMD7', 'Nystagmus, infantile periodic alternating, X-linked', 'NYS1', 'Xlpan', 'FRMD7 congenital nystagmus', 'Nystagmus, infantile idiopathic, formerly', 'nystagmus 1, congenital, X-linked', 'Nystagmus, congenital motor, 1']",0111790,310700,,C1839580,,,,C537853,,,,
mondo:0010694,"nystagmus, myoclonic","['myoclonic nystagmus', 'nystagmus, myoclonic']",,310800,,C1839579,,,,C564088,,,,
mondo:0010695,"occipital hair, white lock of","['occipital hair, white lock of']",,310900,,,,,,,,,,
mondo:0010696,"omphalocele, X-linked","['omphalocele, X-linked']",,310980,,C3275625,,,,,,,,
mondo:0010697,"ophthalmoplegia, external, and myopia","['OPEM', 'ophthalmoplegia, external, and myopia', 'myopia-ophthalmoplegia syndrome']",,311000,,C1839577,,,,C564087,,,,
mondo:0010698,optic atrophy 2,"['optic atrophy, non-Leber type, with early onset', 'optic atrophy type 2', 'optic atrophy 2, X-linked', 'non-Leber type optic atrophy with early-onset', 'OPA2', 'optic atrophy 2', 'optic atrophy, X-linked']",0111443,311050,98890,C1839576,,,,C537125,,,,
mondo:0010699,Charcot-Marie-Tooth disease X-linked recessive 5,"['CMTX5', 'Charcot-Marie-Tooth neuropathy X-linked recessive 5', 'Charcot-Marie-Tooth disease, X-linked recessive, type 5', 'optic atrophy, sensorineural hearing loss and polyneuropathy', 'Charcot-Marie-Tooth neuropathy, X-linked recessive, 5', 'Rosenberg-Chutorian syndrome', 'familial opticoacoustic nerve degeneration and polyneuropathy', 'Charcot-Marie-Tooth disease, X-linked recessive, 5, X-linked recessive', 'CMT5X', 'Charcot-Marie-Tooth neuropathy X type 5', 'Charcot-Marie-Tooth disease, X-linked recessive, 5', 'optic atrophy, polyneuropathy, and deafness', 'Charcot-Marie-Tooth disease X-linked recessive type 5', 'X-linked Charcot-Marie-Tooth disease type 5']",0110210,311070,99014,C1839566,"['0.2251', '0.4895', '0.1409', '-0.1924', '0.0527', '-0.1735', '-0.1719', '0.641', '-0.8135', '-0.0953', '0.1343', '0.2754', '-0.1793', '0.1542', '-0.2224', '-0.4155', '-0.088', '-0.2454', '-0.3877', '-0.4424', '-0.02518', '0.2225', '0.33', '0.608', '0.2603', '0.4658', '-0.07764', '-0.1052', '0.08124', '-0.1261', '0.11456', '-0.5586', '0.0327', '0.2244', '-0.07166', '-0.7437', '-0.6294', '-0.2133', '0.2852', '-0.2168', '-1.464', '-0.4836', '-0.3235', '0.459', '-0.06335', '-0.10315', '0.0863', '-0.0241', '-0.1284', '0.2255', '-0.02641', '0.1293', '-0.1818', '-1.216', '0.1918', '-0.3318', '-0.02594', '0.413', '-0.3728', '0.06244', '-0.4858', '0.262', '0.853', '0.9893', '-0.634', '1.119', '-0.01974', '0.841', '-0.6284', '0.5596', '-0.9194', '-0.02989', '0.3948', '-0.5117', '0.95', '0.2474', '-0.48', '0.4617', '0.158', '-0.2454', '0.1678', '0.0867', '1.02', '0.4807', '0.03824', '0.0603', '0.09973', '0.7964', '0.565', '0.4683', '0.1401', '0.111', '0.1766', '0.3938', '0.536', '0.47', '0.603', '-0.517', '-0.00866', '0.3389']",,,,,,,
mondo:0010700,optic atrophy--spastic paraplegia syndrome,['optic atrophy--spastic paraplegia syndrome'],,311100,,C1839565,,,,C564084,,,,
mondo:0010702,orofaciodigital syndrome I,"['orofaciodigital syndrome 1', 'OFD syndrome 1', 'oral facial digital syndrome type 1', 'Papillon-Leage and Psaume syndrome', 'OFDS 1', 'OFDI', 'Papillon-league-Psaume syndrome (formerly)', 'oral-facial-digital syndrome 1', 'orofaciodigital syndrome type I', 'OFDSI', 'oral-facial-digital syndrome type 1', 'oral facial digital syndrome 1', 'Papillon-Leage-Psaume syndrome', 'orofaciodigital syndrome type 1', 'oral-facial-digital syndrome, type 1', 'OFD1', 'Papillon-Léage-Psaume syndrome', 'orofaciodigital syndrome I', 'orofaciodigital syndrome i, X-linked dominant']",0060316,311200,2750,C2698658,"['0.7607', '0.1722', '0.3308', '-0.457', '0.2029', '-0.09283', '-0.1037', '0.729', '-0.86', '-0.388', '-0.1996', '-0.4392', '0.08154', '0.01904', '-0.3098', '-0.2391', '0.2969', '-0.4167', '-0.429', '-0.0496', '0.0675', '0.01854', '0.4822', '-0.4238', '-0.498', '-0.2542', '-0.4766', '0.1716', '1.173', '-0.6143', '0.4329', '-0.02016', '0.1962', '-0.3042', '0.3726', '-0.3862', '-0.4673', '-0.105', '-0.2947', '-0.101', '0.1923', '-0.325', '0.57', '-0.2485', '0.2732', '-0.1445', '-0.04163', '0.1475', '0.0697', '-0.1788', '-0.3352', '0.3174', '0.02032', '-0.04953', '-0.3264', '0.01347', '0.5283', '-0.1451', '-0.3398', '-0.1214', '0.327', '0.2135', '0.4023', '0.3323', '-0.10175', '-0.2124', '-0.02832', '0.1765', '-0.6494', '-0.193', '-0.4607', '0.3289', '0.1516', '0.1169', '0.3862', '0.05237', '0.2664', '-0.2607', '-0.71', '-0.405', '-0.2773', '0.1571', '0.2323', '0.261', '-0.04745', '0.11536', '-0.2637', '0.3196', '-0.5854', '0.0311', '-0.1881', '0.778', '0.4639', '-0.566', '0.877', '-0.2568', '0.10834', '-0.6875', '0.581', '0.6724']",C75481,,C537134,,,,
mondo:0010703,ornithine carbamoyltransferase deficiency,"['OCT deficiency', 'OTC deficiency', 'ornithine carbamoyltransferase deficiency disease', 'ornithine carbamoyltransferase deficiency', 'deficiency of citrulline phosphorylase', 'OTCD', 'ornithine transcarbamylase deficiency', 'valproate sensitivity', 'ornithine transcarbamylase deficiency, hyperammonemia due to']",9271,311250,664,C0268542,"['0.07263', '0.2379', '-0.4077', '-0.4236', '0.2534', '-0.2878', '-0.2213', '0.4302', '-0.713', '0.527', '-0.314', '-0.5083', '0.3674', '0.8174', '-0.1755', '-0.5586', '-0.0735', '-0.4934', '-0.2236', '-0.9697', '-0.3184', '-0.4731', '0.9736', '-0.3486', '-0.0594', '-0.146', '-0.3296', '-0.3796', '0.1012', '-0.4473', '0.6406', '0.010635', '0.784', '0.561', '-0.638', '0.1942', '-0.1897', '0.0884', '0.06854', '0.2314', '0.00237', '-0.589', '0.5337', '0.2181', '-0.4019', '-0.3335', '-0.2966', '-0.921', '0.2944', '1.036', '-0.3997', '-0.3384', '0.1189', '-0.7095', '0.3364', '0.933', '0.74', '-0.07605', '-0.387', '0.5366', '-0.1252', '0.389', '0.9473', '-0.1198', '0.08813', '0.72', '0.4368', '0.1157', '-0.5635', '0.03378', '-0.1643', '0.3223', '-0.4814', '-0.56', '0.07056', '0.2031', '0.4426', '-0.338', '-0.6426', '-0.010956', '-0.522', '-0.2563', '-0.434', '-0.557', '0.3525', '0.904', '-0.0724', '-0.11847', '0.52', '0.362', '0.05066', '0.6274', '-0.4692', '0.3489', '-0.2191', '0.1573', '0.0561', '-0.3674', '0.245', '0.556']",C84957,0007409,D020163,,,10052450,
mondo:0010704,otopalatodigital syndrome type 1,"['Taybi syndrome', 'oto-palato-digital syndrome type 1', 'OPD 1 syndrome', 'OPD1', 'frontootopalatodigital osteodysplasia', 'otopalatodigital syndrome, type I', 'OPD syndrome 1', 'otopalatodigital syndrome, type 1', 'otopalatodigital syndrome, type I, X-linked dominant', 'OPD syndrome', 'OPD I syndrome', 'otopalatodigital spectrum disorder']",0111783,311300,90650,,"['-0.1349', '-0.0965', '0.464', '-0.4658', '0.5938', '-0.69', '0.5913', '0.8857', '-0.625', '-0.0548', '0.0408', '-0.3413', '-0.1799', '0.03674', '-0.1749', '0.1991', '0.646', '-0.2864', '-0.0798', '-0.0574', '-0.00745', '-0.02756', '1.064', '-0.1953', '0.0944', '-0.07166', '-0.522', '-0.3762', '0.4531', '-0.2278', '0.2944', '-0.4663', '0.2708', '0.2117', '0.2622', '-0.6865', '-0.415', '-0.6494', '-0.3647', '-0.297', '0.3618', '-0.3833', '-0.346', '-0.02292', '0.1536', '-0.42', '-0.2068', '0.824', '-0.3604', '0.12054', '0.000847', '0.0654', '-0.0512', '0.1141', '-0.2021', '-0.5317', '-0.02293', '-0.4749', '0.325', '-0.04037', '-0.0171', '-0.08325', '-0.07074', '-0.10986', '-0.2335', '-0.1898', '-0.07526', '0.1487', '-0.2458', '-0.10767', '-0.2583', '-0.07214', '0.656', '-0.148', '-0.21', '0.795', '0.1606', '0.1912', '-0.493', '-0.3591', '0.4448', '-0.222', '0.145', '0.7793', '-0.4524', '0.4138', '-0.195', '0.568', '0.2477', '0.3765', '-0.2213', '0.6284', '0.4167', '0.531', '0.739', '-0.01631', '0.5146', '-0.952', '0.611', '0.2798']",C118845,,,759.89,,,
mondo:0010706,premature ovarian failure 1,"['fragile x-associated primary ovarian insufficiency', 'fragile X-associated primary ovarian insufficiency', 'familial premature ovarian failure', 'hypergonadotropic ovarian failure, X-linked', 'idiopathic familial premature ovarian failure', 'premature ovarian failure, X-linked', 'ovarian failure, premature', 'premature ovarian failure 1', 'primary ovarian failure caused by mutation in FMR1', 'FMR1 primary ovarian failure', 'FMR1-related primary ovarian insufficiency', 'FMR1-related premature ovarian failure', 'Pof1', 'premature ovarian failure type 1']",0080857,311360,642691,,,,,,256.39,,,
mondo:0010707,Paine syndrome,"['Seemanova syndrome 1', 'Paine syndrome', 'microcephaly with spastic diplegia']",,311400,,C1412041,,,,C538101,,,,
mondo:0010708,Pallister-W syndrome,"['W syndrome', 'median cleft upper lip, mental retardation and pugilistic facies', 'Pallister-W syndrome', 'median cleft upper lip, intellectual disability and pugilistic facies', 'Pallister W syndrome']",,311450,2804,C0796110,,,,C538106,,,,
mondo:0010709,early-onset parkinsonism-intellectual disability syndrome,"['basal ganglion disorder with intellectual disability', 'Waisman syndrome', 'basal ganglia disorder with mental retardation', 'Parkinsonism, early onset with intellectual disability', 'basal ganglia disorder with intellectual disability', 'X-linked recessive basal ganglia disorder with mental retardation', 'BGMR', 'Laxova Brown hogan syndrome', 'X-linked recessive basal ganglia disorder with intellectual disability', 'Waisman syndrome, X-linked recessive', 'Wsn', 'WSMN', 'Parkinsonism, early-onset, with mental retardation', 'basal ganglion disorder with mental retardation', 'Parkinsonism, early-onset, with intellectual disability', 'WAISMAN syndrome', 'Laxova-Opitz syndrome', 'Parkinsonism, early onset with mental retardation']",0111781,311510,2379,C0796195,"['-0.415', '0.467', '-0.11145', '-0.559', '-0.1437', '-0.7227', '0.0657', '0.595', '-0.513', '0.0357', '0.0004666', '-0.00992', '0.1048', '-0.3196', '0.6587', '0.3171', '0.3608', '-0.2183', '-0.5273', '-0.5674', '-0.1118', '0.1316', '0.008156', '-0.05835', '0.4053', '-0.2883', '-0.2568', '0.1196', '-0.1848', '-0.2456', '0.0923', '-0.2532', '0.524', '-0.345', '0.2788', '0.1015', '-0.8657', '-0.379', '-0.1018', '-0.1376', '0.731', '-0.1063', '0.00845', '-0.4316', '0.3335', '-0.1721', '-0.007507', '-0.1472', '-0.6055', '-0.5454', '0.1406', '0.3843', '-0.3823', '-0.4265', '0.1921', '-0.06885', '0.527', '-0.006874', '-0.2622', '0.2783', '0.0711', '-0.2162', '0.3652', '-0.03796', '-0.4202', '0.2103', '0.362', '0.3694', '-0.4048', '0.3767', '-0.2218', '0.3928', '-0.001319', '0.072', '-0.0634', '0.3352', '0.3618', '0.03372', '-0.23', '-0.4016', '-0.24', '-0.057', '0.05978', '0.3552', '0.3445', '-0.05273', '0.1957', '0.929', '0.164', '0.2927', '-0.1473', '0.8555', '0.2292', '-0.1803', '0.5825', '0.1148', '0.3545', '-0.0642', '0.3027', '0.2012']",,,C537179,,,,
mondo:0010710,Pierre Robin syndrome-faciodigital anomaly syndrome,"['Robin sequence with facial and digital anomalies', 'Chitayat Meunier Hodgkinson syndrome', 'Pierre Robin sequence with facial and digital anomalies', 'Chitayat-Meunier-Hodgkinson syndrome', 'Pierre Robin sequence-faciodigital anomaly syndrome', 'Pierre Robin syndrome, faciodigital anomaly']",,311895,2888,C2931064,,,,C535926,,,,
mondo:0010711,TARP syndrome,"['tarp syndrome', 'TARP syndrome, X-linked recessive', 'Pierre Robin syndrome with congenital heart malformation and clubfoot', 'talipes equinovarus - atrial septal defect - Robin sequence - persistence of the left superior vena cava', 'talipes equinovarus-atrial septal defect-Robin sequence-persistence of the left superior vena cava syndrome', 'talipes equinovarus, atrial septal defect, Robin sequence, and persistence of left Superior vena cava', 'Pierre Robin sequence-congenital heart defect-talipes syndrome', 'Pierre Robin syndrome-congenital heart defect-talipes syndrome', 'Pierre Robin syndrome - congenital heart defect - talipes', 'TARPS', 'Pierre Robin sequence - congenital heart defect - talipes']",0111780,311900,2886,C1839463,"['-0.2761', '-0.3992', '-0.178', '0.1011', '0.343', '-0.6504', '-0.329', '0.6753', '-0.05112', '-0.348', '-0.03625', '-0.295', '0.511', '0.3228', '-0.119', '-0.2052', '-0.569', '-0.5054', '-0.4812', '-0.1045', '0.3235', '0.516', '0.652', '-0.226', '0.641', '0.03848', '-0.3093', '0.4197', '0.4736', '0.1373', '0.12427', '-0.567', '0.775', '0.7617', '0.2512', '-0.2102', '-0.1788', '-0.2878', '0.005756', '-0.3857', '0.11945', '0.327', '-0.4138', '-0.1647', '0.03656', '-0.0415', '-0.1797', '0.401', '-0.2903', '-0.3123', '-0.04572', '-0.2595', '-0.4702', '0.428', '-0.6367', '-0.0251', '0.06', '-0.185', '-0.2874', '0.3645', '0.3335', '0.2996', '0.07367', '0.564', '-0.627', '0.2158', '0.388', '0.0965', '-0.2908', '0.3433', '-0.5693', '0.285', '0.04886', '0.17', '0.04678', '-0.09', '0.4685', '-0.321', '-0.925', '0.2196', '0.05237', '0.2517', '0.3826', '0.4246', '0.0118', '-0.2664', '0.655', '0.4067', '0.2517', '-0.09296', '0.372', '0.338', '0.5547', '0.001873', '0.3584', '-0.003654', '0.3994', '-0.1798', '0.3052', '0.4634']",,,C536942,,,,
mondo:0010712,"panhypopituitarism, X-linked","['PHPX', 'pituitary dwarfism IV (formerly)', 'pituitary dwarfism IV', 'pituitary dwarfism IV, formerly', 'panhypopituitarism, X-linked', 'panhypopituitarism X-linked']",0111779,312000,,,,,,C538613,,,,
mondo:0010713,"properdin deficiency, X-linked","['PFD', 'properdin deficiency, X-linked, X-linked recessive', 'complement Factor properdin deficiency', 'properdin deficiency, type 2', 'properdin deficiency, type 3', 'CFPD', 'properdin P Factor deficiency', 'properdin deficiency, type 1', 'properdin deficiency, X-linked']",0111768,312060,2966,,"['-0.3188', '-0.0823', '-0.1315', '-0.1868', '0.1443', '-0.10876', '0.1376', '-0.129', '-0.2695', '0.00878', '0.068', '0.2283', '0.02573', '-0.01365', '0.0936', '-0.000696', '-0.07526', '0.04266', '-0.3833', '-0.4543', '0.1887', '-0.2393', '0.8384', '0.1054', '0.04752', '0.1157', '-0.159', '0.02693', '-0.1924', '-0.1619', '0.297', '0.193', '0.3752', '0.0991', '0.0726', '-0.08594', '-0.10834', '0.0611', '-0.2031', '-0.289', '0.1547', '0.0659', '0.1456', '-0.1562', '-0.07367', '-0.4812', '0.1448', '-0.127', '0.07587', '0.1576', '-0.1126', '-0.1075', '0.1177', '-0.2783', '-0.3225', '-0.03137', '0.3643', '-0.2433', '-0.1727', '0.069', '-0.05014', '0.1315', '0.3232', '0.11884', '0.458', '0.1835', '0.2603', '0.3323', '-0.331', '0.2273', '-0.05496', '-0.07166', '-0.054', '0.02806', '0.0413', '-0.0227', '0.2996', '0.2834', '0.1884', '-0.023', '-0.1277', '-0.08264', '-0.01854', '0.3665', '-0.0638', '-0.353', '0.2423', '0.12354', '0.227', '-0.05698', '0.2515', '-0.04315', '-0.1141', '-0.1492', '0.7163', '0.5454', '0.2429', '-0.539', '-0.1202', '-0.02335']",,,C537241,279.8,,,
mondo:0010714,Pelizaeus-Merzbacher disease,"['Pelizaeus-Merzbacher brain sclerosis', 'Pelizaeus-Merzbacher disease', 'leukodystrophy, hypomyelinating, 1', 'HLD1', 'leukodystrophy, sudanophilic', 'sudanophilic leukodystrophy, Paelizeus-Merzbacher type', 'hypomyelinating leukodystrophy 1', 'PMD', 'Sudanophilic leukodystrophy, Paelizeus-Merzbacher type', 'Pelizaeus Merzbacher disease', 'diffuse familial brain sclerosis', 'Pelizaeus-Merzbacher disease, X-linked recessive', 'Pelizaeus Merzbacher brain sclerosis']",3210,312080,702,C0205711,"['0.0952', '0.5327', '0.203', '-0.1056', '-0.0579', '-0.511', '-0.2783', '0.844', '-0.509', '-0.08936', '-0.763', '-0.2527', '0.2225', '0.408', '0.2654', '-0.4294', '-0.33', '-0.6943', '0.346', '-0.7837', '0.1197', '-0.4443', '0.7764', '-0.254', '0.0889', '-0.144', '0.1312', '0.3418', '0.02599', '0.1252', '0.2646', '0.6973', '0.872', '-0.10626', '-0.218', '-0.2776', '-0.66', '-0.558', '-0.2683', '-0.1095', '0.563', '-0.4004', '0.0605', '0.5195', '0.604', '-0.2241', '-0.2703', '-0.4739', '-0.3347', '-0.4526', '-0.447', '0.0785', '-0.569', '-0.4004', '0.2195', '-0.1864', '0.5356', '0.4849', '-0.505', '0.5015', '-0.5273', '0.1969', '0.788', '0.57', '0.01198', '0.05045', '0.10333', '0.1576', '-0.4763', '0.4048', '0.05927', '-0.2279', '0.6304', '-0.1037', '0.607', '-0.00827', '-0.08453', '-0.3015', '0.1388', '-0.3423', '0.2305', '-0.183', '-0.3477', '0.622', '-0.0602', '0.2764', '0.08264', '-0.1469', '-0.06006', '0.2128', '0.3032', '0.3774', '0.486', '0.6816', '0.179', '-0.1', '-0.0052', '-0.2441', '0.6504', '-0.3188']",C75487,,D020371,,,10067610,
mondo:0010716,X-linked lethal multiple pterygium syndrome,"['pterygium syndrome multiple X-linked', 'multiple pterygium syndrome, X-linked', 'lethal multiple pterygium syndrome, X-linked', 'pterygium syndrome, multiple, X-linked', 'multiple pterygium syndrome X-linked']",,312150,79447,C1839440,,,,C564072,,,,
mondo:0010717,pyruvate dehydrogenase E1-alpha deficiency,"['ataxia with lactic acidosis 1', 'pyruvate dehydrogenase Complex deficiency', 'ataxia, intermittent, with pyruvate dehydrogenase deficiency', 'ataxia, intermittent, with pyruvate dehydrogenase, or decarboxylase, deficiency', 'pyruvate dehydrogenase E1-ALPHA deficiency', 'pyruvate dehydrogenase e1-alpha deficiency, X-linked dominant', 'ataxia, intermittent, with abnormal pyruvate metabolism', 'pyruvate decarboxylase deficiency', 'pyruvate dehydrogenase complex E1 component subunit alpha deficiency', 'PDHAD', 'PDH deficiency', 'pyruvate dehydrogenase E1-alpha deficiency', 'lactic acidemia, thiamine-responsive']",,312170,79243,,"['-0.844', '0.4395', '-0.02557', '0.04993', '0.2059', '-0.277', '-0.266', '0.3855', '-0.551', '-0.004208', '-0.3293', '-0.4822', '-0.05585', '-0.3767', '0.03995', '0.1835', '0.2385', '-0.1332', '-0.7886', '-0.4075', '0.2983', '0.0609', '0.8594', '-0.2966', '0.6187', '0.02023', '0.0962', '0.157', '-0.4375', '0.1744', '0.4265', '0.1967', '0.37', '-0.07135', '-0.2181', '0.1956', '-0.005478', '-0.2128', '-0.5645', '0.3003', '0.0839', '-0.4214', '-0.006588', '0.05664', '0.262', '-0.4116', '-0.02214', '-0.3948', '0.4756', '0.305', '-0.3232', '-0.3235', '-0.504', '0.0728', '-0.2471', '-0.1385', '0.797', '-0.3118', '-0.3887', '0.415', '-0.2001', '-0.1454', '0.693', '0.322', '-0.2546', '-0.04605', '0.1278', '0.0658', '-0.1128', '0.201', '-0.07587', '-0.1707', '0.2805', '-0.1089', '-0.2043', '0.1871', '0.752', '0.4011', '-0.1335', '0.454', '0.3752', '-0.678', '-0.1246', '-0.3003', '0.4187', '0.1395', '0.3503', '0.0781', '0.2302', '0.0686', '0.2927', '0.8516', '-0.01328', '0.1311', '0.984', '0.7046', '0.2544', '0.269', '0.3328', '-0.06128']",,,C564071,277.6,,,
mondo:0010718,absent radius-anogenital anomalies syndrome,"['radius absent anogenital anomalies', 'radial aplasia, X-linked', 'radial aplasia and anogenital anomalies']",,312190,3016,C1839410,,,,C535281,,,,
mondo:0010719,radiation sensitivity of natural killer activity,"['radiation sensitivity of natural killer activity', 'X-Ray Nk sensitivity']",,312210,,C1839408,,,,C564066,,,,
mondo:0010720,partial androgen insensitivity syndrome,"['familial incomplete Male pseudohermaphroditism, type 1', 'Reifenstein syndrome, partial', 'type I familial incomplete male pseudohermaphroditism', 'androgen insensitivity syndrome, partial', 'Reifenstein syndrome', 'androgen resistance syndrome, partial', 'incomplete male pseudohermaphroditism', 'pais', 'androgen insensitivity, partial', 'androgen insensitivity, partial, with or without breast cancer', 'pseudohermaphroditism, incomplete male, type I', 'partial androgen resistance syndrome', 'androgen insensitivity, partial, with or without breast cancer, X-linked recessive', 'PAIS']",0080776,312300,90797,CN035075,"['-0.389', '0.0775', '-0.327', '-0.2355', '0.522', '-0.582', '-0.1797', '0.512', '-0.5605', '-0.4878', '0.00626', '-0.06445', '0.3103', '0.822', '0.1315', '-0.4055', '0.2856', '0.07806', '-0.5127', '-0.768', '-0.757', '0.09393', '1.071', '0.0912', '0.554', '-0.02078', '0.10864', '0.3755', '0.517', '-0.807', '0.2352', '-0.4077', '0.3237', '0.2913', '-0.561', '-0.559', '-0.1925', '-0.2837', '-0.1536', '-0.619', '0.673', '-0.1853', '0.05612', '-0.1807', '-0.02415', '-0.687', '-0.2854', '-0.4812', '0.1705', '0.6626', '0.07465', '-0.8315', '-0.274', '0.2288', '-0.3384', '0.6514', '0.1659', '-0.2344', '-0.5776', '0.05164', '-0.3179', '0.1942', '0.1182', '0.6206', '0.3853', '0.243', '0.3687', '-0.1536', '0.0251', '0.002392', '-0.09314', '0.1404', '0.6216', '0.3647', '0.607', '-0.2148', '0.2037', '-0.0597', '-0.5938', '-0.1753', '-0.2106', '0.7666', '-0.05142', '-0.02617', '-0.02444', '0.0921', '-0.0454', '-0.4583', '0.00936', '0.1803', '-0.2761', '0.911', '-0.8237', '-0.07355', '0.514', '-0.5405', '0.3557', '-0.581', '-0.1754', '0.338']",C120192,,C538435,,E34.52,,
mondo:0010721,"reticuloendotheliosis, X-linked","['reticuloendotheliosis', 'reticuloendotheliosis, X-linked']",,312500,,C0035288,,,,C538362,,,,
mondo:0010722,X-linked retinal dysplasia,"['retinal dysplasia X-linked', 'PRD', 'retinal dysplasia, primary']",,312550,1852,C4275241,,,,,,,,
mondo:0010723,retinitis pigmentosa 2,"['retinitis pigmentosa 2', 'RP2', 'RP2 retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in RP2', 'retinitis pigmentosa type 2']",0110415,312600,,C2681923,,,,C567523,,H35.5,,
mondo:0010725,X-linked retinoschisis,"['X-linked juvenile retinoschisis 1', 'X-linked juvenile retinoschisis', 'juvenile X-linked retinoschisis', 'XLRS1', 'XLRS', 'retinoschisis, X-linked recessive', 'X-linked retinoschisis', 'RS1', 'retinoschisis X-linked', 'retinoschisis, X-linked', 'retinoschisis 1, X-linked, juvenile', 'juvenile retinoschisis', 'XJR', 'X-linked juvenile retinoschisis type 1', 'retinoschisis juvenile X chromosome-linked', 'RS']",0060763,312700,792,,"['-0.5093', '-0.1121', '-0.01997', '0.0105', '0.2563', '-0.1207', '-0.10364', '1.067', '-0.816', '-0.369', '-0.336', '-0.428', '-0.2036', '0.7593', '0.4214', '-0.3708', '-0.1731', '-0.0262', '-0.04584', '-0.734', '-0.297', '0.1704', '0.5405', '-0.3716', '-0.2874', '0.574', '-0.113', '0.263', '0.472', '0.665', '0.5396', '-0.02899', '0.3865', '0.293', '0.0629', '0.277', '0.05344', '-0.543', '-0.3057', '-0.2333', '0.7095', '-0.1003', '0.517', '-0.2303', '0.2803', '-0.1561', '-0.1522', '-0.612', '-0.1047', '0.0176', '0.5503', '0.4626', '0.01202', '-0.3499', '0.6733', '-0.008644', '1.01', '0.1763', '-0.5034', '-0.1074', '0.131', '-0.1658', '0.549', '0.8613', '0.299', '0.1798', '0.3535', '0.8164', '0.257', '0.703', '-0.1843', '-0.2153', '-0.4038', '-0.03513', '0.4', '-0.5786', '0.3704', '0.01938', '-0.175', '-0.0961', '0.2803', '-0.3354', '0.1417', '1.02', '-0.02888', '-0.1603', '0.4424', '-0.1237', '-0.183', '0.142', '0.28', '0.4524', '-0.6553', '0.1497', '0.6772', '-0.343', '0.1278', '-0.5557', '0.3723', '0.1442']",C75483,,,,,,
mondo:0010726,Rett syndrome,"['autism, dementia, ataxia, and loss of purposeful hand use', 'Rett syndrome, atypical', 'RTT', 'Rett syndrome', 'rett syndrome, X-linked dominant', 'Rett syndrome, Zappella variant', 'cerebroatrophic hyperammonemia', 'rett syndrome, atypical, X-linked dominant', 'rett syndrome, preserved speech variant, X-linked dominant', 'Rett syndrome, preserved speech variant', 'Rts', 'Rett^s disorder']",1206,312750,778,C0035372,"['-0.04257', '-0.007576', '-0.1147', '0.6206', '-0.1263', '-0.527', '0.4492', '0.9194', '-0.1587', '-0.425', '-0.2097', '0.008', '-0.0405', '0.659', '0.672', '0.06854', '-0.02963', '0.287', '-0.2311', '-0.4507', '-0.2085', '-0.2952', '0.1517', '-0.536', '0.3816', '-0.5864', '0.0662', '0.1665', '0.003254', '0.719', '0.5703', '-0.4639', '0.7256', '0.3223', '-0.4087', '-0.1616', '-0.3877', '0.1066', '0.2644', '0.1667', '0.5767', '0.079', '-0.3223', '0.3916', '0.561', '-0.6763', '-0.8906', '0.207', '0.4045', '0.681', '-0.7266', '-0.1299', '-0.596', '-0.2854', '0.1772', '-0.5874', '-0.373', '0.4512', '-0.2166', '0.05768', '0.2646', '0.1938', '0.3345', '0.751', '-0.4233', '-0.05298', '0.2147', '0.2622', '-0.1631', '0.672', '0.1007', '0.01889', '-0.223', '-0.551', '0.02715', '0.4429', '-0.4485', '0.3552', '-0.00141', '0.03503', '0.3247', '-0.2279', '0.2252', '0.0992', '0.365', '0.01357', '0.3643', '0.3623', '0.705', '0.4873', '-0.2583', '0.02205', '0.0952', '0.626', '-0.1902', '0.03543', '0.186', '-0.564', '0.8203', '0.1581']",C75488,,D015518,330.8,,10039000,
mondo:0010727,"Russell-silver syndrome, X-linked","['Russell-silver syndrome, X-linked', 'Partington syndrome', 'Russell-Silver-like syndrome with skin pigmentation']",,312780,,,,,,,758.81,,,
mondo:0010728,SCARF syndrome,"['skeletal abnormalities, cutis laxa, craniostenosis, ambiguous genitalia, retardation, and Facial abnormalities', 'SCARF syndrome']",,312830,3134,C1839321,,,,C536625,,,,
mondo:0010729,"X-linked intellectual disability, Schimke type","['choreoathetosis with mental retardation X- linked', 'choreoathetosis with mental retardation, X-linked', 'childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and mental retardation, ophthalmoplegia, and deafness', 'progressive basal ganglion dysfunction, mental and growth retardation, external ophthalmoplegia, postnatal microcephaly and deafness', 'childhood-onset choreoathetosis with spasticity, postnatal microcephaly, growth and intellectual disability, ophthalmoplegia, and deafness', 'Schimke X-linked mental retardation syndrome', 'choreoathetosis with intellectual disability, X-linked', 'choreoathetosis with intellectual disability X- linked', 'Schimke X-linked intellectual disability syndrome']",,312840,85285,C1839320,,,,C536630,,,,
mondo:0010730,"combined immunodeficiency, X-linked","['CIDX', 'immunodeficiency 6', 'Xcid', 'combined immunodeficiency, X-linked, moderate, X-linked recessive', 'combined immunodeficiency, X-linked']",,312863,,,,,,,,,,
mondo:0010731,Simpson-Golabi-Behmel syndrome,"['Golabi-Rosen syndrome', 'SGB syndrome', 'DGSX', 'dysplasia gigantism syndrome, X-linked', 'Sgbs', 'Sara Angers syndrome', 'SDYS', 'SGBS', 'X-linked dysplasia gigantism syndrome']",,,373,,"['0.2053', '0.302', '0.2556', '-0.703', '0.3025', '-0.262', '0.0218', '0.3608', '-0.7812', '-0.5513', '-0.0617', '0.4536', '0.4788', '-0.4624', '-0.3215', '0.2411', '-0.0705', '-0.4438', '-0.2966', '-0.522', '0.4143', '0.006077', '0.4001', '-0.4153', '-0.2715', '-0.5034', '-0.1149', '0.3728', '0.86', '-0.716', '0.491', '0.4512', '0.7407', '-0.3232', '-0.12286', '-0.505', '-0.0742', '-0.09644', '-0.11115', '0.00722', '-0.397', '-0.11865', '0.926', '-0.1654', '-0.1946', '-0.2878', '-0.1558', '0.11237', '-0.1672', '-0.1598', '-0.7134', '0.4136', '-0.599', '0.2676', '-0.391', '-0.263', '-0.1904', '0.0796', '-0.676', '0.0639', '0.1594', '0.1423', '-0.12445', '-0.156', '0.393', '0.2754', '-0.02385', '0.7466', '-0.731', '-0.0696', '-0.1967', '0.153', '0.0153', '0.1775', '-0.01735', '-0.6494', '0.05374', '0.04507', '-0.5825', '-0.667', '-0.5786', '0.294', '-0.3064', '0.362', '-0.6587', '0.1154', '0.2266', '-0.0553', '0.05627', '0.0722', '-0.05612', '0.1057', '0.0208', '-0.3657', '0.949', '-0.0227', '0.705', '-0.3577', '0.97', '-0.05975']",C131002,,C537340,759.89,,,
mondo:0010732,spastic paraparesis-deafness syndrome,"['spastic paraparesis - deafness', 'familial spastic paraparesis and deafness', 'Wells-Jankovic syndrome', 'spastic paraparesis and deafness']",0081100,312910,2815,C2931291,,,,C536692,,G11.4,,
mondo:0010733,hereditary spastic paraplegia 2,"['SPG2', 'hereditary spastic paraplegia type 2', 'X-linked spastic paraplegia type 2', 'spastic paraplegia 2', 'X-linked spastic paraplegia 2', 'PLP1 hereditary spastic paraplegia', 'spastic gait type 2', 'spastic paraparesis type 2', 'spastic paraplegia 2, X-linked', 'spastic paraplegia type 2', 'hereditary spastic paraplegia caused by mutation in PLP1', 'Sppx2', 'spastic paraplegia 2, X-linked, X-linked recessive']",0110773,312920,99015,C1839264,"['0.2825', '0.2183', '0.05148', '-0.2235', '-0.1462', '-0.578', '-0.3767', '0.7207', '-0.8604', '-0.681', '-0.3066', '-0.2834', '-0.1068', '0.3113', '0.632', '-0.2471', '-0.2439', '-0.757', '0.1068', '-0.6377', '0.8647', '-0.4631', '0.414', '-0.0652', '-0.4917', '-0.549', '-0.1718', '-0.2888', '0.1929', '-0.3706', '0.6445', '0.2913', '0.1392', '-0.3313', '-0.43', '-0.7856', '-0.2883', '-0.4314', '0.03226', '-0.39', '0.814', '-0.7246', '0.1092', '0.091', '0.2361', '0.1885', '-0.282', '-0.5635', '-0.255', '0.2324', '-0.3606', '0.594', '-0.9624', '-0.651', '-0.1986', '0.4966', '0.934', '0.05884', '-0.2068', '0.736', '-0.09406', '0.6313', '0.8467', '0.7153', '-0.03644', '0.5684', '0.2019', '0.1935', '-0.255', '0.553', '-0.4814', '0.4443', '0.0377', '-0.3113', '0.88', '-0.09503', '-0.1735', '0.3132', '0.3394', '-0.06464', '-0.1873', '-0.45', '0.08246', '0.562', '-0.3772', '0.3665', '0.05496', '-0.1786', '0.0882', '-0.2358', '0.1587', '0.1589', '0.07086', '-0.3286', '0.4165', '-0.0839', '-0.3718', '-0.4153', '0.738', '-0.01425']",,,,,,,
mondo:0010734,"spatial visualization, aptitude for","['Turner syndrome-associated Neurocognitive phenotype', 'visuospatial/perceptual abilities', 'spatial visualization, aptitude for', 'visuospatial/perceptual abilities, X-linked recessive', 'Turner syndrome-associated neurocognitive phenotype, X-linked recessive']",,313000,,C1839262,,,,C564058,,,,
mondo:0010735,Kennedy disease,"['spinobulbar muscular atrophy', 'spinal and bulbar muscular atrophy, X-linked type 1', 'bulbospinal muscular atrophy, X-linked', 'X-linked bulbo-spinal atrophy', 'X-linked bulbospinal muscular atrophy', 'X-linked bulbospinal amyotrophy', 'spinal and bulbar muscular atrophy of Kennedy, X-linked recessive', 'Kennedy spinal and bulbar muscular atrophy', 'bulbospinal neuronopathy, X-linked recessive', 'spinal and bulbar muscular atrophy', 'spinal and bulbar muscular atrophy, X-linked 1', 'X-linked spinal and bulbar muscular atrophy', 'Kennedy^s disease', 'X-linked BSMA', 'SMAX1', 'spinal bulbar muscular atrophy', 'SBMA', 'Kennedy disease']",0060161,313200,481,C1839259,"['-0.317', '0.01061', '0.215', '-0.542', '-0.07245', '-0.5713', '0.07733', '0.728', '-0.8555', '-0.5923', '0.0903', '-0.0407', '-0.794', '0.3594', '0.9326', '0.2146', '-0.01428', '-0.587', '-0.4375', '-0.711', '-0.0783', '-0.471', '-0.183', '0.1783', '-0.2104', '0.196', '0.3743', '0.1707', '-0.0152', '-0.4792', '0.518', '0.199', '0.5005', '-0.534', '0.2568', '-0.3088', '0.5034', '-0.06854', '0.01468', '0.254', '-0.00955', '-0.2708', '0.03442', '0.0806', '-0.09717', '0.02539', '-0.12427', '-0.4365', '-0.1564', '0.822', '-0.4739', '-0.081', '0.3901', '-0.0397', '-0.005516', '-0.0834', '0.455', '0.05225', '-0.3638', '0.1998', '0.0694', '0.0563', '0.01996', '-0.218', '-0.1263', '0.09314', '0.3591', '0.11035', '0.08105', '0.0992', '-0.6626', '-0.6025', '0.2153', '0.07513', '0.832', '-0.01136', '-0.3535', '-0.1525', '-0.2264', '-0.0618', '0.366', '-0.2632', '0.4238', '0.258', '-0.00411', '0.2756', '0.2905', '-0.2522', '0.6377', '-0.2686', '-0.1041', '0.0632', '0.01436', '0.1729', '0.726', '-0.2474', '0.0852', '0.263', '0.2006', '-0.07117']",C85233,,D055534,,,10068600,
mondo:0010736,split hand-foot malformation 2,"['split hand foot anomaly - X-linked', 'SHFD2', 'SHSF2', 'SHFM2', 'split hand-foot malformation type 2', 'split-hand/split-foot anomaly, X-linked', 'split-hand/foot deformity 2', 'split-hand/foot malformation 2', 'split hand/foot malformation X-linked', 'split hand foot deformity 2', 'split hand/foot malformation 2']",0090027,313350,,,,,,C564056,,,,
mondo:0010737,"spondyloepiphyseal dysplasia tarda, X-linked","['spondyloepiphyseal dysplasia, late', 'SED', 'X linked spondyloepiphyseal dysplasia tarda', 'spondyloepiphyseal dysplasia tarda, X-linked recessive', 'Sed tarda, X-linked', 'SEDT', 'spondyloepiphyseal dysplasia tarda X-linked', 'spondyloepiphyseal dysplasia tarda, X-linked', 'X-linked spondyloepiphyseal dysplasia']",0080362,313400,,,,,,,,,,
mondo:0010738,"spondylometaphyseal dysplasia, Golden type","['spondylometaphyseal dysplasia, Richmond type', 'spondylometaphyseal dysplasia, X-linked', 'X-linked spondylometaphyseal dysplasia', 'spondylometaphyseal dysplasia X-linked', 'spondylometaphyseal dysplasia Richmond type']",,313420,168544,C0796172,,,,C563124,,,,
mondo:0010739,Taqi polymorphism,"['TAQ1', 'Taqi polymorphism', 'TaqI polymorphism']",,313480,,,,,,,,,,
mondo:0010740,"taurodontism, microdontia, and dens invaginatus","['taurodontism, microdontia, and dens invaginatus']",,313490,,C1839235,,,,C536947,,,,
mondo:0010741,"tooth agenesis, selective, X-linked, 1","['tooth agenesis, selective, X-linked 1, X-linked dominant', 'tooth agenesis caused by mutation in EDA', 'tooth agenesis, selective, X-linked, 1', 'EDA tooth agenesis', 'STHAGX1', 'tooth agenesis, selective, X-linked, type 1', 'hypodontia/oligodontia, X-linked, 1']",,313500,,C1970757,,,,C567060,,,,
mondo:0010742,pentalogy of Cantrell,"['Cantrell Haller Ravitsch syndrome', 'Cantrell syndrome', 'Cantrell pentalogy', 'Tas', 'thoracoabdominal syndrome', 'pentalogy of Cantrell', 'thoraco-abdominal syndrome', 'Midline defects, X-linked', 'THAS', 'Cantrell deformity']",,313850,1335,C0559483,,C99011,,D058502,759.89,,,
mondo:0010743,thrombocytopenia 1,"['thrombocytopenia, X-linked, intermittent', 'THC', 'XLT', 'thrombocytopenia, X-linked, 1', 'X-linked thrombocytopenia with normal platelets', 'THC1', 'thrombocytopenia, X-linked, intermittent, X-linked recessive', 'thrombocytopenia type 1', 'thrombocytopenia, X-linked', 'thrombocytopenia 1', 'thrombocytopenia, X-linked, X-linked recessive', 'X-linked thrombocytopenia']",,313900,852,C1839163,"['-0.1055', '0.12213', '0.01191', '-0.03217', '0.0929', '-0.03674', '-0.02945', '0.1691', '-0.03574', '-0.1311', '-0.009575', '-0.02963', '0.0828', '-0.00765', '-0.001805', '-0.0468', '-0.0374', '-0.00827', '-0.04047', '-0.1942', '-0.01056', '-0.02414', '0.1523', '-0.04938', '0.07306', '-0.04828', '-0.02513', '-0.03162', '0.0348', '-0.0672', '0.08276', '0.01086', '0.1592', '0.0885', '-0.02568', '-0.076', '-0.1054', '-0.10144', '-0.02654', '-0.1414', '-0.003462', '-0.0778', '0.02002', '-0.10406', '-0.06073', '-0.1649', '-0.02432', '0.02997', '0.04614', '-0.02829', '-0.007683', '-0.02344', '0.0548', '0.00797', '-0.05255', '-0.02495', '0.1075', '-0.11176', '-0.1461', '-0.012505', '0.08374', '0.01747', '0.04785', '0.01758', '0.015236', '-0.04855', '0.1071', '0.1066', '-0.117', '0.162', '-0.1083', '-0.0203', '-0.06305', '-0.10504', '0.0822', '0.03638', '0.0644', '-0.05777', '-0.0256', '-0.0799', '-0.0625', '-0.03656', '-0.005207', '0.05716', '-0.0643', '0.0489', '0.06213', '0.1321', '0.0818', '-0.01178', '0.02809', '0.1494', '-0.01034', '0.04117', '0.19', '0.1357', '0.04266', '-0.2261', '0.03693', '0.05084']",C176617,,C564052,,,,
mondo:0010744,thrombocytopenia with elevated serum IgA and renal disease,['thrombocytopenia with elevated serum IgA and renal disease'],,314000,,C1839162,,,,C564051,,,,
mondo:0010745,beta-thalassemia-X-linked thrombocytopenia syndrome,"['thrombocytopenia, Platelet dysfunction, hemolysis, and Imbalanced globin synthesis', 'thrombocytopenia with BETA-thalassemia, X-linked', 'X-linked thrombocytopenia with Beta-thalassemia', 'XLTT', 'thrombocytopenia with beta-thalassemia, X-linked, X-linked recessive']",0111767,314050,231393,C1839161,"['-0.4104', '0.1262', '-0.02402', '-0.689', '-0.04233', '-0.5415', '-1.088', '1.225', '-0.9995', '-1.008', '0.002352', '0.313', '0.3662', '0.793', '-0.1625', '-0.073', '-1.316', '-0.2162', '-0.5415', '-0.8804', '-0.2087', '-0.2585', '1.025', '-0.3704', '0.761', '-0.2383', '0.4326', '-0.3699', '0.6665', '-0.4878', '0.0046', '-0.3157', '0.1964', '-0.432', '-0.4888', '-0.5767', '-0.802', '-0.2335', '-0.3599', '-0.9087', '0.4866', '0.1871', '0.4778', '-0.0803', '-0.8594', '-0.6553', '-0.759', '-0.99', '0.616', '-0.6216', '-0.1692', '-0.7427', '0.2496', '0.1979', '-0.01566', '0.2556', '-0.3682', '1.153', '-0.3242', '0.4333', '-0.5615', '-0.239', '0.08704', '-0.3774', '-0.3423', '-0.03436', '0.1874', '0.7466', '-1.028', '0.728', '0.0547', '0.4248', '-0.1863', '-0.07684', '0.516', '0.1547', '0.02066', '0.0433', '0.11523', '0.2708', '-0.446', '-0.839', '0.2418', '-0.3838', '-0.1675', '0.158', '0.407', '0.3833', '0.09784', '0.3035', '0.4167', '0.3684', '0.0551', '-0.04904', '0.79', '0.5664', '-0.6216', '-0.3406', '-0.1769', '-0.7886']",C134941,,C564050,,,,
mondo:0010746,"thumbs, congenital Clasped","['thumbs, congenital Clasped', 'Clasped thumbs, congenital', 'adducted thumbs syndrome']",,314100,,CN074234,,,,,,,,
mondo:0010747,X-linked dystonia-parkinsonism,"['dystonia 3, torsion, X-linked', 'Lubag', 'dystonia-Parkinsonism, X-linked', 'X-linked dystonia-parkinsonism/Lubag', 'dystonia-Parkinsonism, X-linked, X-linked recessive', 'DYT-TAF1', 'XDP', 'torsion dystonia-Parkinsonism, Filipino type', 'Lubag syndrome', 'X-linked dystonia-Parkinsonism syndrome', 'X-linked dystonia Parkinsonism', 'DYT3', 'X-linked torsion dystonia-Parkinsonism syndrome']",0090057,314250,53351,C1839130,"['0.507', '0.103', '-0.3794', '-0.1442', '-0.2688', '-0.6265', '0.2268', '0.4875', '-0.8247', '-0.3228', '0.634', '0.5703', '-0.2842', '0.6577', '0.525', '0.4941', '-0.04218', '-0.9326', '-0.3513', '-0.6133', '-0.536', '-0.00645', '0.07526', '-0.2852', '-0.462', '0.04462', '-0.1746', '-0.016', '0.00832', '0.03162', '0.1893', '0.2389', '0.6514', '-0.04733', '0.5244', '-0.12213', '0.6763', '-0.4258', '-0.05524', '-0.3308', '0.4746', '-0.0997', '-0.05762', '0.418', '0.5996', '-0.02531', '-0.5444', '0.1399', '0.2512', '0.273', '-0.04916', '0.1741', '0.7344', '-0.3137', '0.842', '0.2065', '0.6245', '0.4548', '0.1116', '-0.2053', '-0.4207', '-0.2954', '-0.03622', '-0.597', '-0.7217', '0.5894', '0.3174', '0.1621', '-0.4004', '0.4258', '-0.004276', '-0.572', '-0.05548', '0.1276', '0.1652', '0.301', '0.7197', '-0.2004', '0.1577', '-0.277', '0.09143', '-0.2822', '0.9414', '0.2795', '0.561', '0.6016', '0.3188', '0.3171', '1.363', '-0.1414', '0.02704', '0.1508', '0.09735', '0.4353', '0.946', '-0.008125', '-0.06125', '0.2837', '0.5527', '-0.49']",C126330,,C564048,,,,
mondo:0010748,torticollis-keloids-cryptorchidism-renal dysplasia syndrome,"['Tkcr syndrome', 'Goeminne TKCR syndrome', 'Goeminne syndrome', 'Tkc', 'torticollis keloids cryptorchidism renal dysplasia', 'TKCR', 'torticollis, keloids, cryptorchidism, and renal dysplasia']",,314300,3341,C1839129,,,,C536970,,,,
mondo:0010749,trigonocephaly-short stature-developmental delay syndrome,"['Say Meyer syndrome', 'trigonocephaly, short stature, and retarded psychomotor development', 'trigonocephaly with short stature and developmental delay', 'Say-Meyer syndrome', 'trigonocephaly, short stature and developmental delay']",,314320,3369,,,,,C536620,,,,
mondo:0010750,ulnar hypoplasia-split foot syndrome,"['severe ulnar aplasia and lobster claw feet', 'ulnar hypoplasia with lobster-claw deformity of feet', 'complete absence of the ulna and of fingers 2 to 5, together with lobster-claw deformity of the feet', 'ulnar hypoplasia-lobster-claw deformity of feet syndrome', 'ulnar hypoplasia lobster claw deformity of feet', 'familial ulnar aplasia and lobster claw syndrome', 'Van De Berghe Dequeker syndrome', 'Van den Berghe-Dequecker syndrome']",,314360,1122,C1839123,,,,C536936,,,,
mondo:0010751,unique green phenomenon,['unique green phenomenon'],,314380,,C1839116,,,,,,,,
mondo:0010752,"VACTERL association, X-linked, with or without hydrocephalus","['VACTERL association with hydrocephaly, X-linked', 'VACTERL association, X-linked, with or without hydrocephalus', 'VACTERL-H, X-linked', 'VACTERLX', 'X-linked VACTERL-H syndrome', 'VACTERL association, X-linked, X-linked recessive']",0111766,314390,,C2931228,,,,,,,,
mondo:0010753,"cardiac valvular dysplasia, X-linked","['CVD1', 'valvular heart disease, congenital', 'myxomatous valvular dystrophy, X-linked', 'XMVD', 'congenital valvular dysplasia', 'cardiac valvular dysplasia, X-linked']",0111765,314400,555877,,"['-0.1329', '0.1036', '0.008606', '-0.0882', '0.2069', '-0.3499', '-0.0819', '0.1094', '-0.1715', '-0.2517', '0.03812', '-0.03099', '0.00873', '-0.10254', '-0.1465', '-0.1332', '-0.2444', '-0.1242', '-0.2091', '-0.3352', '0.1074', '0.1243', '0.3125', '-0.05557', '0.1631', '-0.03053', '-0.00878', '0.02339', '0.1897', '-0.08636', '0.207', '0.0488', '0.1842', '-0.01906', '0.0686', '-0.3289', '0.0855', '-0.1467', '0.0667', '-0.2212', '0.00793', '-0.1252', '0.02888', '0.1337', '-0.1599', '-0.2375', '-0.04562', '0.09344', '0.1588', '-0.0773', '-0.01782', '-0.1326', '0.116', '0.05817', '-0.0445', '-0.2474', '0.2822', '0.1039', '-0.2476', '0.1349', '0.1349', '0.2554', '-0.0008545', '-0.0721', '0.0777', '-0.00696', '0.1559', '0.198', '-0.4434', '-0.003778', '-0.2441', '-0.165', '0.07214', '-0.0628', '-0.01791', '-0.01569', '0.05417', '0.157', '-0.1691', '0.0811', '0.07355', '0.05148', '-0.0116', '0.05307', '-0.0522', '-0.001934', '0.2236', '0.3018', '0.1483', '0.1198', '-0.1769', '0.011734', '0.02948', '0.0899', '0.4858', '0.2124', '0.3284', '-0.3623', '0.1101', '0.02931']",,,C535576,,,,
mondo:0010754,van den Bosch syndrome,"['van den Bosch syndrome', 'mental deficiency, choroideremia, acrokeratosis verruciformis,anhidrosis, skeletal deformity']",,314500,3417,C0796192,,,,C563129,,,,
mondo:0010755,"vesicoureteral reflux, X-linked","['vesicoureteral reflux, X-linked', 'VURX']",,314550,,C1839114,,,,C564042,,,,
mondo:0010756,"Von Willebrand disease, X-linked form","['Von Willebrand disease, X-linked', 'Von Willebrand disease, X-linked form']",,314560,,C1839113,,,,C564041,,,,
mondo:0010757,widow^s peak syndrome,"['widow^s peak syndrome', 'widow^s peak, ptosis, and skeletal anomalies']",,314570,,C1839112,,,,C564040,,,,
mondo:0010758,Wieacker-Wolff syndrome,"['Wieacker-Wolff syndrome, X-linked recessive', 'apraxia, oculomotor, with congenital contractures and muscle atrophy', 'mental retardation, X-linked, with congenital contractures and low fingertip arches', 'Wieacker-Wolff syndrome', 'mental retardation, X-linked, with congenital contractures and Low fingertip arches', 'X-linked intellectual disability, Miles-Carpenter type', 'Miles-Carpenter syndrome', 'foot contractures-muscle atrophy-oculomotor apraxia syndrome', 'intellectual disability-developmental delay-contractures syndrome', 'WRWF', 'MRXS4', 'WRWFXLR', 'Wieacker-Wolff syndrome, X-linked', 'MCS', 'contractures of feet, muscle atrophy, and oculomotor apraxia', 'Wieacker Wolff syndrome', 'Miles-CARPENTER X-linked mental retardation syndrome', 'Wieacker syndrome', 'mental retardation, X-linked, syndromic 4']",0060815,314580,85283,,"['-0.708', '-0.0759', '0.1628', '-0.1978', '0.3772', '-0.834', '-0.359', '0.883', '-0.4524', '-0.3726', '-0.06104', '-0.1693', '-0.05405', '0.06238', '0.09827', '0.2164', '0.579', '0.409', '-0.579', '-0.4824', '0.3538', '0.2218', '0.0512', '0.1122', '0.04855', '-0.12396', '0.08905', '-0.02307', '0.308', '-0.742', '0.5728', '-0.5483', '0.267', '0.1456', '-0.03174', '-0.749', '-0.4297', '-0.4497', '-0.2593', '-0.401', '0.00411', '-0.6567', '-0.4219', '-0.0747', '-0.4502', '-0.687', '0.2041', '0.031', '-0.781', '-0.2096', '-0.4167', '-0.1769', '-0.002115', '-0.1416', '-0.0763', '-0.6626', '0.3564', '-0.09454', '-0.1029', '0.206', '-0.1945', '-0.555', '0.1048', '0.4678', '-0.7715', '0.3452', '-0.3303', '0.9565', '-0.8677', '0.05524', '-0.5967', '0.05875', '0.0766', '-0.1284', '-0.11316', '0.1654', '-0.4526', '0.271', '-0.4822', '0.1311', '0.5054', '0.5938', '0.2144', '0.476', '0.1277', '0.2983', '0.07715', '0.532', '0.0791', '-0.1242', '-0.0779', '0.6323', '0.4353', '-0.2427', '0.763', '0.418', '-0.10297', '-0.767', '0.2546', '0.06055']",,,C537472,,,,
mondo:0010759,Wildervanck syndrome,"['Wildervanck syndrome', 'COA syndrome', 'cervico-oculo-acoustic dysplasia', 'Cervicooculoacoustic syndrome', 'cervico-oculo-acoustic syndrome']",,314600,3456,C0265239,,,,,759.89,,10069402,
mondo:0010760,XH antigen,['XH antigen'],,314800,,,,,,C009691,,,,
mondo:0010761,retinitis pigmentosa Y-linked,"['Y-linked retinitis pigmentosa', 'RPY', 'retinitis pigmentosa, Y-linked', 'retinitis pigmentosa, y-linked, y-linked']",0110418,400004,,C1839079,,,,C564035,,H35.5,,
mondo:0010762,"lymphoma, Hodgkin, Y-linked pseudoautosomal","['Hodgkin disease, Y-linked Pseudoautosomal', 'lymphoma, Hodgkin, Y-linked pseudoautosomal']",,400021,,C1839076,,,,C564034,,,,
mondo:0010763,"spermatogenic failure, Y-linked, 1","['Sertoli cell-only syndrome, Y-linked', 'spermatogenic failure, Y-linked, 1, Y-linked', 'incomplete Sertoli cell-only syndrome', 'SPGFY1', 'spermatogenic failure, Y-linked, 1', 'Sertoli cell-only syndrome, type 1', 'spermatogenic failure, Y-linked, type 1', 'Sertoli cell-only syndrome, type 2', 'hypospermatogenesis']",0070186,400042,,C0028960,,,,,,,,
mondo:0010764,"hearing loss, Y-linked 1","['deafness, Y-linked 1', 'deafness, y-linked 1, y-linked', 'DFNY1']",0111759,400043,,C3888076,,,,,,,,
mondo:0010765,"46,XY complete gonadal dysgenesis","['46,XY gonadal dysgenesis', 'gonadal dysgenesis, XY female type', '46,XY SEX reversal', 'pure gonadal dysgenesis 46,XY', 'sex-reversing locus on X, formerly', '46, XY complete gonadal dysgenesis', '46, XY pure gonadal dysgenesis', '46, XY CGD', 'sex-reversing locus on X', 'Swyer syndrome', '46 XY gonadal dysgenesis', 'testis-determining Factor, X-chromosomal', '46,XY CGD', '46,XY pure gonadal dysgenesis']",14448,,242,C2936694,"['0.343', '-0.0433', '-0.133', '-0.408', '0.3076', '-0.156', '0.10724', '0.522', '-0.5566', '-0.4272', '0.274', '-0.3696', '-0.0784', '0.4487', '-0.157', '-0.4082', '0.2598', '0.03986', '-0.5366', '-0.9937', '-0.375', '-0.1891', '0.9604', '-0.5913', '0.11664', '0.3225', '-0.11035', '0.4402', '0.505', '-0.49', '0.5347', '0.1064', '0.676', '0.1791', '-0.4587', '-0.2328', '0.2903', '-0.1836', '-0.2054', '-0.1794', '1.082', '0.32', '0.0856', '-0.2517', '0.1744', '-0.4287', '-0.3218', '-0.576', '0.468', '0.533', '-0.1636', '-0.449', '-0.01932', '-0.096', '-0.1881', '0.253', '-0.05072', '-0.5874', '-0.316', '0.0327', '0.3442', '0.319', '0.224', '0.0623', '0.0592', '0.594', '0.356', '0.2537', '-0.09564', '0.5', '-0.11523', '0.2703', '0.03094', '-0.1549', '-0.11145', '-0.4885', '-0.0585', '0.1031', '-0.5254', '-0.5454', '0.1661', '0.4707', '0.0982', '0.1572', '-0.2905', '-0.2979', '-0.05795', '-0.4941', '0.2251', '-0.0204', '0.07635', '0.4324', '-0.4949', '0.03047', '0.6895', '-0.3594', '0.1693', '0.0749', '-0.1716', '-0.001267']",C120198,,D006061,,,,
mondo:0010767,"spermatogenic failure, Y-linked, 2","['oligozoospermia, nonobstructive, Y-linked', 'spermatogenic failure, Y-linked, 2, Y-linked', 'SPGFY2', 'spermatogenic failure, Y-linked, type 2', 'Azf regions', 'azoospermia Factor regions', 'azoospermia, nonobstructive, Y-linked', 'spermatogenic failure, Y-linked, 2', 'spermatogenic arrest, Y-linked', 'spermatogenic failure, nonobstructive, Y-linked', 'oligospermia, nonobstructive, Y-linked']",0070187,415000,,,,,,C564030,,,,
mondo:0010768,gonadoblastoma,"['gonadoblastoma', 'gonad blastoma']",3301,,,C0206661,,C3754,,D018238,,,,
mondo:0010769,"hairy ears, Y-linked","['hairy ears, Y-linked, Y-linked', 'hairy ears, Y-linked', 'hypertrichosis pinnae auris, Y-linked']",,425500,,C1839070,,,,C564029,,,,
mondo:0010770,"ubiquitin-activating enzyme, Y-linked","['Ube1Y', 'ubiquitin-activating enzyme, Y-linked']",,489000,,,,,,,,,,
mondo:0010771,histiocytoid cardiomyopathy,"['focal lipid cardiomyopathy', 'infantile histiocytoid cardiomyopathy', 'myocardial hamartoma', 'Arachnocytosis of the myocardium', 'oncocytic cardiomyopathy', 'infantile cardiomyopathy with histiocytoid change', 'foamy myocardial transformation of infancy', 'histiocytoid cardiomyopathy', 'infantile xanthomatous cardiomyopathy', 'cardiomyopathy, focal Lipid', 'cardiomyopathy, infantile histiocytoid', 'Purkinje cell hamartoma', 'cardiomyopathy, oncocytic', 'cardiomyopathy, infantile xanthomatous', 'congenital cardiomyopathy', 'isolated Cardiac lipidosis']",0080198,500000,137675,CN239812,"['0.323', '-0.5786', '-0.062', '0.5967', '-0.08673', '-0.619', '0.562', '0.5747', '-0.09247', '-0.4604', '0.0794', '-0.255', '-0.3303', '0.23', '-0.502', '0.3447', '-0.7993', '-0.04236', '-0.4875', '-0.7427', '0.2218', '0.5415', '0.5327', '-0.1359', '0.3362', '-0.3428', '0.09955', '0.6904', '-0.0709', '-0.4612', '0.9307', '-0.3298', '0.759', '0.2255', '0.1731', '-0.574', '0.132', '-0.297', '0.548', '-0.4531', '0.2079', '0.567', '-0.00393', '0.1665', '0.3333', '0.524', '-0.003975', '0.676', '0.3455', '-0.391', '-0.188', '0.1407', '0.674', '0.097', '0.537', '-0.2625', '-0.3154', '0.1103', '-0.7466', '0.0645', '-0.11285', '0.5654', '0.3352', '-0.9175', '-0.874', '0.1951', '-0.0335', '0.475', '-0.6973', '0.03114', '-0.3494', '0.3247', '-0.0665', '-0.08795', '-0.0393', '0.2856', '-0.317', '-0.3962', '-0.5044', '0.3547', '0.1328', '-0.2727', '0.003698', '-0.509', '1.081', '-0.4321', '0.4287', '0.0379', '0.2637', '0.12067', '0.1536', '0.1228', '-0.2393', '0.2122', '1.052', '0.628', '0.2654', '-0.516', '-0.4734', '-0.2947']",C45745,,C535584,,,,
mondo:0010772,Leber optic atrophy and dystonia,"['Leber optic atrophy and dystonia', 'dystonia familial, with visual failure and striatal lucencies', 'Leber^s hereditary optic neuropathy with dystonia', 'dystonia, familial, with visual failure and striatal lucencies', 'Leber hereditary optic neuropathy with dystonia', 'Marsden syndrome', 'LHON and dystonia', 'LDYT', 'Leber Hereditary optic neuropathy with dystonia']",0111755,500001,,C1839040,,,,C536024,,,,
mondo:0010773,myopathy and diabetes mellitus,"['mitochondrial myopathy with diabetes', 'mitochondrial myopathy, lipid type']",,500002,2596,C1839028,,,,C564026,,,,
mondo:0010774,"striatonigral degeneration, infantile, mitochondrial","['infantile bilateral striatal Necrosis, mitochondrial', 'striatonigral degeneration, infantile, mitochondrial', 'bilateral striatal Necrosis, infantile, mitochondrial']",,500003,,C1839022,,,,C564025,,,,
mondo:0010775,retinitis pigmentosa-deafness syndrome,"['retinitis pigmentosa 8', 'retinitis pigmentosa-deafness syndrome', 'RP21, formerly', 'retinitis pigmentosa 21', 'retinitis pigmentosa 21, formerly', 'retinitis pigmentosa 8, formerly', 'RP8, formerly']",0110829,500004,231183,CN033130,"['0.01328', '0.2666', '0.0277', '0.1075', '0.1483', '-0.5195', '0.12415', '0.799', '-0.3137', '-0.2153', '-0.24', '0.03754', '-0.3232', '0.0944', '0.05878', '-0.5327', '0.001254', '-0.212', '0.1321', '-0.3635', '-0.1361', '-0.3555', '0.0649', '0.2019', '0.215', '-0.04645', '-0.6978', '-0.05267', '-0.527', '0.1865', '0.6143', '-0.1715', '-0.2698', '0.4355', '-0.0628', '-0.0329', '-0.1238', '-0.1737', '-0.2532', '0.2053', '0.03577', '0.1965', '0.1857', '0.1849', '0.002935', '-0.0326', '-0.1416', '-0.010185', '0.08344', '0.3389', '0.1377', '0.3406', '-0.2213', '-0.201', '0.2452', '-0.1103', '0.233', '-0.3577', '-0.0998', '0.2384', '0.01582', '0.0381', '0.2742', '0.001309', '-0.5386', '0.02864', '0.254', '0.759', '-0.1885', '0.4927', '-0.329', '-0.01413', '0.2151', '-0.353', '0.6094', '-0.419', '-0.0669', '0.3179', '-0.2008', '-0.03525', '0.11786', '-0.2358', '0.1107', '0.6875', '-0.2272', '-0.206', '0.3738', '0.2341', '0.2673', '0.4023', '0.2944', '0.777', '0.4253', '0.319', '0.1698', '-0.07684', '0.4224', '-0.558', '0.2034', '0.1991']",,,,,H35.5,,
mondo:0010776,"hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial","['hypomagnesemia, hypertension, and hypercholesterolemia, mitochondrial']",,500005,,C1839021,,,,C564024,,,,
mondo:0010777,"cardiomyopathy, infantile hypertrophic",,0111753,500006,,C2748884,,,,,,,,
mondo:0010778,cyclic vomiting syndrome,"['cyclic vomiting syndrome-plus', 'cyclic vomiting syndrome', 'CVS', 'cyclic vomiting syndrome with neuromuscular disease', 'Cvs-plus']",,500007,,,,,,,,,,
mondo:0010779,mitochondrial non-syndromic sensorineural hearing loss,"['mitochondrial non-syndromic sensorineural deafness', 'deafness, nonsyndromic sensorineural, mitochondrial', 'deafness, isolated, due to mitochondrial transmission', 'mitochondrial non-syndromic neurosensory deafness', 'isolated mitochondrial sensorineural deafness', 'isolated mitochondrial neurosensory deafness']",0111751,500008,90641,,"['-0.12305', '0.0953', '0.1636', '-0.01599', '0.0963', '-0.1567', '0.0212', '0.301', '-0.1136', '-0.1126', '-0.0889', '-0.1456', '-0.0804', '-0.005566', '-0.0995', '-0.152', '0.04797', '-0.0713', '-0.07605', '-0.2512', '-0.001903', '-0.08496', '0.07355', '0.00881', '0.1642', '0.0446', '-0.1066', '-0.04105', '0.04977', '-0.0499', '0.0761', '0.1334', '0.191', '0.128', '-0.0498', '-0.1473', '-0.04813', '-0.1959', '-0.09686', '-0.129', '0.0893', '-0.1654', '0.0742', '-0.02904', '-0.0754', '-0.1309', '-0.0982', '0.0814', '0.00886', '0.1138', '-0.0629', '-0.0333', '0.04184', '-0.1381', '-0.04462', '-0.11896', '0.1869', '-0.1257', '-0.1779', '0.07367', '0.0805', '0.007435', '0.03015', '0.05646', '-0.1312', '-0.05478', '0.078', '0.2583', '-0.1514', '0.263', '-0.2009', '0.06445', '0.1095', '-0.1125', '0.10443', '-0.02017', '0.1167', '0.005913', '-0.1166', '-0.00757', '0.0621', '-0.05856', '-0.05203', '0.2168', '0.00972', '-0.0484', '0.05292', '0.2437', '0.0981', '0.1268', '0.2053', '0.2979', '0.0735', '0.0873', '0.298', '0.014366', '0.2573', '-0.2812', '0.0818', '0.1137']",,,,,,,
mondo:0010780,mitochondrial myopathy with reversible cytochrome C oxidase deficiency,"['reversible infantile respiratory chain deficiency', 'benign COX deficiency', 'reversible infantile cytochrome C oxidase deficiency', 'mitochondrial myopathy with reversible COX deficiency', 'Cox deficiency myopathy, infantile, transient', 'infantile reversible cytochrome C oxidase deficiency myopathy', 'mitochondrial myopathy, infantile, transient, due to respiratory chain deficiency', 'respiratory chain deficiency, infantile, transient', 'MMIT', 'mitochondrial myopathy with reversible complex IV deficiency', 'mitochondrial myopathy, infantile, transient']",,500009,254864,C3151898,,,,,,,,
mondo:0010781,"ataxia and polyneuropathy, adult-onset",,0111750,500010,,C1838916,,,,C564020,,,,
mondo:0010782,"myopathy, lactic acidosis, and sideroblastic anemia 3","['myopathy, lactic acidosis, and sideroblastic anemia type 3', 'myopathy, lactic acidosis, and sideroblastic anemia 3', 'MLASA3', 'myopathy, lactic acidosis, and sideroblastic anaemia type 3']",0111184,500011,,C4225415,,,,,,,,
mondo:0010784,chloramphenicol toxicity,"['anemia, chloramphenicol-induced', 'chloramphenicol toxicity', 'chloramphenicol resistance']",,515000,,,,,,,,,,
mondo:0010785,maternally-inherited diabetes and deafness,"['Ballinger Wallace syndrome', 'diabetes mellitus type II with deafness', 'Niddm with deafness', 'maternally inherited diabetes and deafness', 'mitochondrial diabetes', 'Ballinger-Wallace syndrome', 'noninsulin-dependent diabetes mellitus with deafness', 'diabetes and deafness, maternally inherited', 'diabetes-deafness syndrome, maternally Transmitted', 'MIDD', 'diabetes mellitus, type II, with deafness']",,520000,225,C4330695,,C131859,,C536246,250.80,,,
mondo:0010786,chronic diarrhea with villous atrophy,"['diarrhea, chronic, with villous atrophy']",,520100,1670,C1838912,,,,C564019,,K59.1,,
mondo:0010787,Kearns-Sayre syndrome,"['Kearns-Sayre syndrome', 'CPEO with ragged-Red fibres', 'mitochondrial Cytopathy', 'oculocraniosomatic syndrome', 'CPEO with ragged-Red fibers', 'ophthalmoplegia plus syndrome', 'ophthalmoplegia, pigmentary Degeneration of retina, and cardiomyopathy', 'ophthalmoplegia, progressive external, with ragged red fibres', 'ophthalmoplegia, progressive external, with ragged-Red fibers', 'CPEO with ragged red fibers', 'ophthalmoplegia, progressive external, with ragged-Red fibres', 'ophthalmoplegia-plus syndrome', 'KSS', 'ophthalmoplegia, progressive external, with ragged red fibers', 'CPEO with ragged red fibres', 'CPEO with myopathy', 'chronic progressive external ophthalmoplegia with myopathy']",12934,530000,480,C0022541,,C84798,,D007625,,,10048804,
mondo:0010788,Leber hereditary optic neuropathy,"['Leber^s hereditary optic neuropathy', 'optic atrophy, Leber type', 'LHON', 'Leber’s disease', 'Leber^s optic atrophy', 'Leber optic atrophy', 'Leber Hereditary optic atrophy', 'Leber hereditary optic neuropathy']",705,535000,104,C0917796,"['0.01516', '0.03668', '-0.374', '0.619', '-0.1445', '-0.452', '0.1349', '0.6987', '0.033', '-0.02231', '0.5283', '0.225', '0.0723', '0.1885', '0.5146', '-0.3462', '-0.1619', '-0.1173', '0.2673', '-0.523', '-0.1826', '-1.055', '0.1299', '-0.3389', '0.09827', '-0.1687', '-0.869', '0.5596', '-0.803', '0.2499', '0.6655', '0.3682', '0.2281', '-0.02684', '-0.1218', '-0.5005', '0.2764', '-0.9727', '-0.3147', '-0.2266', '0.3271', '-0.3635', '-0.1547', '-0.3296', '-0.1489', '-0.0794', '-0.757', '-0.243', '-0.232', '0.5034', '-0.08325', '0.276', '-0.201', '-0.64', '0.3694', '-0.1954', '0.507', '-0.1935', '-0.5293', '0.291', '-0.1084', '-0.176', '0.7754', '0.843', '-0.7456', '-0.03111', '0.681', '0.5547', '0.2285', '0.797', '0.2664', '0.2253', '0.7134', '0.1914', '0.4807', '-0.03513', '0.2542', '0.2996', '-0.1116', '-0.1375', '0.0937', '-0.183', '-0.562', '0.5405', '-0.271', '-0.245', '0.191', '-0.1189', '0.3584', '0.0805', '0.5894', '0.1494', '-0.0792', '0.2656', '0.413', '0.01678', '0.2013', '0.2766', '0.1192', '-0.1892']",C84808,,D029242,,,,
mondo:0010789,MELAS syndrome,"['mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes', 'mitochondrial encephalomyopathy lactic acidosis and stroke-like episodes', 'MELAS syndrome', 'MELAS', 'mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes', 'mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes', 'mitochondrial encephalomyopathy, lactic acidosis and stroke']",3687,540000,550,C0162671,"['-0.3228', '0.3079', '-0.1306', '-0.2527', '0.3206', '-0.463', '0.682', '0.4473', '-0.3787', '0.053', '-0.2588', '-0.4312', '0.245', '0.1418', '0.1288', '-0.004383', '-0.0907', '-0.1927', '-1.104', '-0.769', '0.1777', '-0.9165', '-0.03394', '-0.0552', '-0.0478', '-0.2493', '-0.3347', '-0.541', '0.0651', '-0.03693', '0.723', '0.1173', '0.6934', '0.215', '0.2133', '-0.2363', '-0.1472', '-0.0805', '-0.0973', '0.4424', '0.223', '-0.3936', '0.9863', '-0.03278', '0.431', '-0.1338', '-0.1377', '0.4446', '-0.2095', '0.547', '-0.597', '0.5317', '-0.2078', '-0.7207', '0.3303', '0.04486', '0.5454', '-0.4402', '-0.6006', '0.2612', '-0.06174', '-0.1404', '1.069', '-0.6406', '-0.342', '-0.05215', '-0.0875', '0.09814', '-0.354', '0.6313', '-0.4043', '0.004246', '-0.2498', '0.0265', '0.407', '-0.10126', '0.409', '0.1431', '0.05365', '0.2742', '0.971', '-0.248', '-0.2732', '0.154', '-0.02501', '0.4624', '0.655', '0.1752', '0.1394', '0.3218', '0.545', '-0.0991', '0.11035', '-0.5166', '0.1593', '-0.07007', '0.411', '-0.235', '-0.03174', '0.3904']",C84885,,D017241,277.87,E88.41,10053872,
mondo:0010790,MERRF syndrome,"['myoclonus with epilepsy and with ragged Red fibers (MERRF syndrome)', 'myoclonus with epilepsy and with ragged Red fibers', 'myoclonic epilepsy - ragged red fibres', 'myoclonic epilepsy with ragged red fibers', 'myoclonus with epilepsy and with ragged Red fibres', 'myoclonic epilepsy with ragged red fibres', 'MERRF syndrome', 'myoclonus epilepsy and ragged red fibres', 'myoclonus epilepsy and ragged red fibers', 'myoencephalopathy ragged-red fiber disease', 'myoencephalopathy ragged-red fibre disease', 'myoclonus epilepsy associated with ragged-red fibers', 'MERRF', 'Fukuhara syndrome', 'myoclonus with epilepsy and with ragged Red fibres (MERRF syndrome)', 'myoclonic epilepsy associated with ragged-RED fibres', 'myoclonic epilepsy - ragged red fibers', 'myoclonic epilepsy associated with ragged red fibers', 'myoclonic epilepsy associated with ragged-RED fibers', 'myoclonic epilepsy associated with ragged red fibres', 'myoclonus epilepsy associated with ragged-red fibres']",310,545000,551,C0162672,,C84889,,D017243,277.87,E88.42,10069825,
mondo:0010791,"myoglobinuria, recurrent","['myoglobinuria recurrent', 'myoglobinuria, recurrent']",,550500,,,,,,C564018,,,,
mondo:0010792,lethal infantile mitochondrial myopathy,"['LIMD', 'lethal infantile mitochondrial disease', 'LIMM', 'mitochondrial myopathy, lethal, infantile']",,551000,254857,C1838876,,,,C564017,,,,
mondo:0010793,"nephropathy, chronic tubulointerstitial","['nephropathy, chronic tubulointerstitial']",,551200,,C1838875,,,,C564016,,,,
mondo:0010794,NARP syndrome,"['neuropathy-ataxia-retinitis pigmentosa syndrome', 'NARP', 'NARP syndrome', 'neuropathy, ataxia, and retinitis pigmentosa', 'neurogenic muscle weakness-ataxia-retinitis pigmentosa syndrome', 'neuropathy ataxia retinitis pigmentosa syndrome']",0111273,551500,644,C1328349,"['-0.204', '0.2634', '-0.04645', '-0.07227', '-0.3572', '-0.8', '0.4268', '0.675', '-0.5063', '-0.2399', '-0.2183', '-0.2109', '0.02167', '0.4534', '0.1121', '-0.4016', '-0.10016', '-0.3848', '0.2788', '-0.913', '-0.1912', '-0.2041', '-0.1487', '0.1059', '-0.0754', '-0.2507', '-0.09485', '-0.278', '-0.206', '-0.02992', '0.2474', '0.3674', '0.131', '0.2185', '-0.1757', '-0.233', '0.2076', '-0.2883', '-0.617', '-0.3352', '-0.1998', '-0.279', '0.7544', '0.2161', '0.272', '-0.01851', '-0.1263', '0.188', '0.2162', '0.4998', '-0.3882', '0.6616', '0.4294', '-0.737', '0.7383', '-0.2151', '0.5513', '-0.294', '-0.1729', '0.06714', '0.1807', '0.1726', '0.06012', '-0.0983', '-1.022', '0.1775', '0.07184', '0.447', '-0.2305', '0.4094', '-0.6577', '-0.2095', '0.0819', '-0.112', '0.2903', '-0.2603', '0.5713', '-0.5557', '-0.1699', '-0.1268', '0.9165', '0.0213', '-0.3455', '1.124', '-0.02406', '0.4304', '-0.1532', '-0.3022', '0.398', '0.02579', '0.4717', '-0.2876', '0.166', '0.1704', '0.5083', '-0.4983', '0.407', '0.61', '-0.1489', '0.2595']",,,C537396,,,10062940,
mondo:0010795,oncocytic neoplasm,"['oncocytic neoplasm', 'oncocytoma', 'oncocytic tumour', 'oncocytic tumor', 'oncocytoma, benign']",,553000,,C1378050,,C7072,,,,,,
mondo:0010796,"Parkinson disease, mitochondrial","['Parkinson disease, mitochondrial']",,556500,,C1838867,,,,C564015,,,,
mondo:0010797,Pearson syndrome,"['Pearson^s marrow/pancreas syndrome', 'Pearson marrow-pancreas syndrome', 'Pearson^s syndrome', 'sideroblastic anaemia with marrow cell vacuolization and exocrine pancreatic dysfunction (formerly)', 'sideroblastic Anemia with marrow cell vacuolization and exocrine pancreatic dysfunction', 'sideroblastic anemia with marrow cell vacuolization and exocrine pancreatic dysfunction (formerly)', 'sideroblastic Anaemia with marrow cell vacuolization and exocrine pancreatic dysfunction']",0060067,557000,699,C0342784,,C115326,,,277.87,,10062941,
mondo:0010798,proximal tubulopathy-diabetes mellitus-cerebellar ataxia syndrome,"['renal tubulopathy, diabetes mellitus, and cerebellar ataxia due to duplication of mitochondrial DNA', 'proximal tubulopathy, diabetes mellitus and cerebellar ataxia', 'renal tubulopathy, diabetes mellitus, and cerebellar ataxia']",,560000,3390,C3151959,,,,C564014,,,,
mondo:0010799,"deafness, aminoglycoside-induced","['aminoglycoside-induced deafness', 'mitochondrial isolated neurosensory deafness with susceptibility to aminoglycoside exposure', 'mitochondrial isolated sensorineural deafness with susceptibility to aminoglycoside exposure', 'deafness, aminoglycoside-induced', 'mitochondrial non-syndromic neurosensory hearing loss with susceptibility to aminoglycoside exposure', 'deafness, streptomycin-induced', 'mitochondrial non-syndromic neurosensory deafness with susceptibility to aminoglycoside exposure', 'streptomycin ototoxicity', 'mitochondrial non-syndromic sensorineural hearing loss with susceptibility to aminoglycoside exposure', 'aminoglycoside-induced hearing loss', 'mitochondrial non-syndromic sensorineural deafness with susceptibility to aminoglycoside exposure', 'deafness, mitochondrial, modifier of, mitochondrial', 'mitochondrial isolated sensorineural hearing loss with susceptibility to aminoglycoside exposure', 'mitochondrial isolated neurosensory hearing loss with susceptibility to aminoglycoside exposure']",0111734,580000,168609,C1838854,"['-0.07996', '0.07544', '0.0656', '-0.009834', '0.1346', '-0.1337', '0.0686', '0.1428', '-0.02846', '-0.1032', '0.006306', '-0.04608', '-0.02383', '0.01593', '-0.09656', '-0.1108', '0.0913', '-0.02484', '-0.1259', '-0.2559', '-0.01182', '-0.07214', '0.10876', '-0.0454', '0.0237', '0.01328', '-0.0657', '-0.006413', '-0.0464', '-0.10376', '0.08673', '0.07', '0.1672', '0.08246', '0.00288', '-0.1443', '-0.0885', '-0.1212', '-0.0923', '-0.1437', '0.03555', '-0.0849', '0.07776', '-0.03165', '-0.0729', '-0.1997', '-0.00998', '0.08295', '0.0741', '0.03308', '-0.08594', '-0.08997', '0.12463', '-0.024', '-0.02599', '-0.04773', '0.1512', '-0.0798', '-0.1143', '0.0652', '0.07776', '0.0775', '0.01762', '0.05658', '-0.04007', '0.05145', '0.08563', '0.2471', '-0.1726', '0.278', '-0.1489', '0.01003', '0.0946', '-0.0951', '0.0652', '0.03983', '0.06305', '0.006603', '0.01376', '0.02087', '-0.0103', '-0.0167', '-0.01582', '0.1743', '-0.0335', '-0.04025', '0.045', '0.2275', '0.1262', '0.02939', '0.1549', '0.1636', '-0.04117', '0.03592', '0.2488', '0.08307', '0.206', '-0.2189', '-0.0411', '0.002127']",,,C564013,,,,
mondo:0010800,"Wolfram syndrome, mitochondrial form","['Wolfram syndrome, mitochondrial form', 'diabetes insipidus and mellitus with optic atrophy and deafness, mitochondrial form', 'Didmoad syndrome, mitochondrial form']",0080583,598500,,C1838782,,,,C564012,,,,
mondo:0010801,spondylocamptodactyly syndrome,"['camptodactyly with cervical platyspondyly', 'spondylocamptodactyly', 'spondylo camptodactyly syndrome']",,600000,3180,C4274762,,,,C535779,,,,
mondo:0010802,pancreatic hypoplasia-diabetes-congenital heart disease syndrome,"['heart defects, congenital, and other congenital anomalies', 'pancreatic agenesis and congenital heart defects', 'hereditary pancreatic hypoplasia, diabetes mellitus and congenital heart disease', 'Yorifuji-Okuno syndrome', 'Yorifuji Okuno syndrome', 'pancreatic hypoplasia, congenital, with diabetes mellitus and congenital heart disease', 'HDCA', 'congenital pancreatic hypoplasia with diabetes mellitus and congenital heart disease']",0111733,600001,2255,,"['0.8354', '-0.12317', '0.10474', '0.801', '-0.3877', '-0.9824', '-0.423', '0.943', '0.1755', '-0.643', '0.1241', '-0.2703', '0.166', '0.1678', '-0.9697', '-0.268', '0.4333', '0.2361', '-0.1476', '-0.7505', '0.1416', '-0.10754', '0.1322', '0.067', '-0.697', '-0.2776', '0.1663', '0.00492', '0.6714', '-0.3806', '0.9214', '-0.7656', '0.3398', '-0.1761', '-0.04965', '0.4722', '-0.6333', '0.411', '0.06223', '-0.2455', '0.1498', '0.4375', '0.2942', '0.5825', '-0.4246', '-0.3396', '0.4768', '-0.07196', '-0.01402', '0.2915', '0.1293', '-0.3152', '0.877', '-0.802', '-0.012276', '0.1431', '-0.0678', '-0.745', '-1.06', '0.65', '-0.5996', '0.6177', '-0.2146', '0.1384', '-0.1703', '0.7686', '-0.382', '0.574', '-1.098', '0.11035', '0.4978', '0.2969', '0.1832', '-0.2896', '0.5366', '0.4734', '-0.5615', '0.9287', '-0.3352', '-0.1858', '-0.02022', '0.1151', '0.02737', '-0.4353', '0.2659', '0.2573', '0.08527', '0.6694', '0.662', '0.2134', '0.5586', '0.402', '0.013145', '-0.10645', '1.352', '0.1838', '-0.2017', '-0.1927', '-0.4797', '0.10034']",,,C564011,,,,
mondo:0010803,Eiken syndrome,"['bone modelling defect of hands and feet', 'bone modeling defect of hands and feet', 'Eiken syndrome', 'Eiken skeletal dysplasia']",0111732,600002,79106,C1838779,"['-0.521', '0.1805', '0.276', '-0.02899', '0.5864', '-0.1945', '-0.1575', '0.9536', '-0.3503', '-0.2064', '-0.227', '0.2712', '0.0764', '-0.04858', '0.1105', '0.2133', '0.4841', '0.2659', '-0.3293', '-0.2169', '0.05273', '-0.3286', '0.4329', '-0.177', '0.4082', '0.1636', '-0.1864', '-0.171', '0.1401', '-0.5884', '0.2568', '-0.338', '-0.3022', '-0.03708', '-0.1803', '-0.3467', '-0.3467', '-0.5547', '0.0615', '-0.2212', '0.2742', '-0.1962', '0.03275', '-0.378', '-0.0873', '-0.722', '-0.03748', '0.4092', '-0.4785', '-0.4688', '-0.0981', '-0.05072', '0.0976', '0.1092', '-0.5747', '-0.6997', '-0.04422', '-0.2332', '-0.09485', '0.3115', '0.658', '-0.0797', '-0.02534', '-0.0857', '-0.2668', '-0.0974', '0.3032', '0.554', '-0.359', '-0.315', '-0.0258', '-0.1783', '-0.2544', '0.0323', '0.09753', '0.2751', '-0.3845', '0.593', '0.1438', '-0.3137', '-0.0381', '0.4397', '0.0958', '-0.00694', '-0.257', '0.0157', '-0.1265', '0.03088', '0.5015', '0.1575', '-0.03528', '0.2793', '-0.144', '-0.11597', '0.5063', '0.4438', '0.204', '-1.036', '-0.01962', '0.2996']",,,C564010,,,,
mondo:0010805,bladder exstrophy,"['bladder exstrophy (disease)', 'classic exstrophy of the bladder', 'exstrophy of bladder', 'bladder exstrophy', 'exstrophy of the bladder', 'ectopia vesicae', 'bladder exstrophy and epispadias Complex']",0080174,,93930,C0005689,,C123207,,D001746,753.5,,,0002836
mondo:0010806,retinitis pigmentosa 13,"['retinitis pigmentosa type 13', 'RP13', 'retinitis pigmentosa caused by mutation in PRPF8', 'retinitis pigmentosa 13', 'PRPF8 retinitis pigmentosa', 'RP 13']",0110403,600059,,C1838702,,,,C564008,,H35.5,,
mondo:0010807,autosomal recessive nonsyndromic hearing loss 2,"['autosomal recessive nonsyndromic deafness caused by mutation in MYO7A', 'autosomal recessive nonsyndromic deafness 2', 'MYO7A autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 2', 'deafness, autosomal recessive 2', 'autosomal recessive deafness 2', 'deafness, autosomal recessive type 2', 'DFNB2', 'neurosensory nonsyndromic recessive deafness 2']",0110477,600060,,C1838701,,,,C564007,,,,
mondo:0010808,fatal familial insomnia,"['fatal familial insomnia', 'Insomnia, fatal familial', 'FFI', 'familial fatal insomnia', 'fatal familial INSOMNIA', 'Insomnia familial fatal']",0050433,600072,466,C0206042,"['0.03403', '0.2012', '-0.2974', '0.4683', '-0.3882', '4.077e-05', '0.0977', '1.011', '0.1581', '-0.002726', '0.5493', '0.284', '-0.269', '0.575', '-0.4988', '-0.7837', '-0.772', '0.4658', '-0.7075', '-0.6836', '-0.4873', '-0.4573', '-0.08594', '-0.1094', '0.2534', '-0.4592', '0.1829', '-0.2175', '0.03366', '0.304', '0.606', '-0.2295', '0.2123', '0.5347', '-0.05185', '-0.2267', '-0.631', '-0.126', '0.1656', '-0.4514', '0.7407', '0.01176', '-0.3208', '0.2559', '0.3638', '-0.9165', '-0.3115', '0.2786', '0.338', '1.061', '0.001496', '0.8105', '-0.2607', '0.1023', '0.471', '-0.3347', '0.0293', '0.3572', '-0.4863', '-0.978', '-0.1292', '1.24', '0.2335', '-0.1793', '-0.02812', '0.6597', '-0.06433', '0.446', '0.1809', '0.3574', '-0.2147', '0.3303', '0.286', '-0.6597', '0.1898', '0.07153', '0.349', '0.8354', '-0.2935', '-0.2448', '-0.2429', '-0.1935', '-0.2067', '0.622', '0.8643', '0.2214', '0.0516', '0.2783', '0.8623', '0.4983', '0.1134', '-0.1254', '-0.8', '0.42', '-0.5703', '0.03635', '-0.2202', '-0.156', '-0.3914', '-0.2717']",C84711,,D034062,046.72,A81.83,10072077,
mondo:0010809,familial chronic myelocytic leukemia-like syndrome,"['myelocytic leukemia-like syndrome, familial, chronic', 'familial CML-like syndrome', 'CML-like syndrome, familial']",0060761,600080,,C1838670,,,,C536093,,,,
mondo:0010810,"vitamin D hydroxylation-deficient rickets, type 1B","['rickets due to defect in vitamin D 25-hydroxylation deficiency', 'vitamin D-dependent rickets, type 1B', 'vitamin D-dependent rickets, type 1 caused by mutation in CYP2R1', 'VDDR1B', 'vitamin D 25-Hydroxylase deficiency', '25-Hydroxyvitamin D3 deficiency, selective', 'vitamin D hydroxylation-deficient rickets, type 1B', 'Pseudovitamin D3 deficiency rickets due to 25-Hydroxylase deficiency', 'Vitam D hydroxylation-deficient rickets type 1b', 'CYP2R1 vitamin D-dependent rickets, type 1', 'vitamin D hydroxylation-deficient rickets type 1b']",0080887,600081,,C1838657,,C131074,,C564005,,,,
mondo:0010811,benign prostatic hyperplasia,"['benign prostatic hypertrophy', 'benign prostatic hyperplasia', 'benign hyperplasia of the prostate', 'benign prostatic hyperplasia - BPH', 'BPH', 'benign prostate hyperplasia', 'benign hyperplasia of prostate', 'benign prostatic Hypertrophy', 'benign prostatic hyperplasia (disease)', 'prostatic hyperplasia, benign']",2883,600082,,C1704272,,C2897,0000284,D011470,600.20,,,0008711
mondo:0010812,"macrocytosis, familial","['macrocytosis, familial']",,600084,,C1838656,,,,C564004,,,,
mondo:0010813,pancreatic beta cell agenesis with neonatal diabetes mellitus,"['diabetes mellitus, insulin-dependent, neonatal', 'pancreatic beta cell agenesis with neonatal diabetes mellitus']",,600089,28455,C1838655,,,,C538111,,,,
mondo:0010814,chondrodysplasia-pseudohermaphroditism syndrome,"['Nivelon-Nivelon-Mabille syndrome', 'chondrodysplasia-pseudohermaphroditism syndrome', 'chondrodysplasia-disorder of sex development syndrome']",0060644,600092,1422,C1838654,,,,C536123,,,,
mondo:0010815,spondyloepiphyseal dysplasia tarda with characteristic facies,['spondyloepiphyseal dysplasia tarda with characteristic facies'],0112289,600093,,C1838653,,,,C564003,,,,
mondo:0010816,Qazi Markouizos syndrome,"['Qazi-Markouizos syndrome', 'Dysharmonic skeletal maturation-muscular fibre disproportion syndrome', 'Dysharmonic skeletal maturation muscular fiber disproportion', 'Dysharmonic skeletal maturation - muscular fibre disproportion', 'Dysharmonic skeletal maturation muscular fibre disproportion', 'hypotonia, psychomotor retardation, seizures, delayed and Dysharmonic skeletal maturation, and congenital fibre type disproportion', 'Dysharmonic skeletal maturation-muscular fiber disproportion syndrome', 'Dysharmonic skeletal maturation - muscular fiber disproportion', 'PUERTO RICAN infant hypotonia syndrome', 'Puertorican infant hypotonia syndrome', 'hypotonia, psychomotor retardation, seizures, delayed and Dysharmonic skeletal maturation, and congenital fiber type disproportion']",0050740,600096,3010,C2931142,,,,C536259,,,,
mondo:0010817,autosomal dominant nonsyndromic hearing loss 2A,"['DFNA2A', 'autosomal dominant nonsyndromic deafness 2A', 'autosomal dominant nonsyndromic deafness caused by mutation in KCNQ4', 'autosomal dominant nonsyndromic deafness type 2A', 'deafness, autosomal dominant 2A', 'autosomal dominant deafness 2A', 'KCNQ4 autosomal dominant nonsyndromic deafness', 'deafness, autosomal dominant 2a', 'deafness, autosomal dominant type 2A']",0110558,600101,,C2677637,,,,C567441,,,,
mondo:0010818,retinitis pigmentosa 12,"['retinitis pigmentosa with or without Paraarteriolar preservation of retinal pigment epithelium', 'retinitis pigmentosa 12', 'CRB1 retinitis pigmentosa', 'retinitis pigmentosa-12', 'RP with or without preserved Paraarteriole retinal pigment epithelium', 'retinitis pigmentosa caused by mutation in CRB1', 'RP12', 'retinitis pigmentosa type 12', 'RP with or without Pprpe', 'RP 12']",0110358,600105,,C1838647,,,,C563999,,H35.5,,
mondo:0010819,Stargardt disease 3,"['Stargardt disease 3', 'STGD3', 'macular dystrophy with flecks, type 3', 'Stargardt-like macular dystrophy, autosomal dominant', 'Stargardt disease type 3']",,600110,,C1838644,,,,C535805,,,,
mondo:0010820,autosomal recessive juvenile Parkinson disease 2,"['autosomal recessive juvenile Parkinson^s disease 2', 'JP', 'young-onset Parkinson disease caused by mutation in PRKN', 'Parkinson disease, juvenile, autosomal recessive', 'Parkinsonism, early-onset, with diurnal fluctuation', 'PDJ', 'autosomal recessive juvenile Parkinson disease', 'PRKN young-onset Parkinson disease', 'Parkinson disease 2', 'Parkinson disease autosomal recessive, early onset', 'Parkinson disease 2, autosomal recessive juvenile', 'Parkinsonism, early onset, with diurnal fluctuation', 'Parkinson disease, juvenile, type 2', 'autosomal recessive juvenile Parkinson disease type 2', 'PARK2', 'juvenile parkinsonism']",0060368,600116,,C1868675,,,,,,,,
mondo:0010821,familial developmental dysphasia,"['specific language impairment', 'developmental dysphasia familial', 'developmental language disorder', 'dysphasia, familial developmental', 'FOXP2-associated dysphasia', 'Billard-Toutain-Maheut syndrome']",,600117,1799,C1838630,,,,C563997,,F80.1,,
mondo:0010822,Warburg micro syndrome 1,"['WARBM1', 'micro syndrome 1', 'micro syndrome', 'Warburg micro syndrome caused by mutation in RAB3GAP1', 'Warburg micro syndrome type 1', 'RAB3GAP1 Warburg micro syndrome', 'WARBURG micro syndrome 1', 'Warburg micro syndrome 1']",0110716,600118,,,,,,,,,,
mondo:0010823,rhizomelic chondrodysplasia punctata type 3,"['rhizomelic chondrodysplasia punctata type 3', 'alkylglycerone-phosphate synthase deficiency', 'RCDP3', 'AGPS rhizomelic chondrodysplasia punctata', 'rhizomelic chondrodysplasia punctata, type 3', 'AGPS deficiency', 'alkyldihydroxyacetonephosphate synthase deficiency', 'rhizomelic chondrodysplasia punctata caused by mutation in AGPS']",0110853,600121,309803,C1838612,"['-0.4873', '0.3599', '0.1676', '-0.2493', '0.2651', '-0.4148', '-0.0969', '0.09894', '-0.6206', '-0.09625', '-0.0995', '0.289', '0.0814', '-0.09735', '0.1697', '-0.03815', '0.1316', '-0.008194', '-0.211', '-0.4678', '0.05182', '0.1172', '0.392', '-0.1918', '-0.04575', '0.2874', '0.015305', '-0.07477', '0.1587', '0.01591', '-0.07513', '-0.01997', '0.1205', '0.07135', '0.11774', '0.1251', '0.01036', '-0.251', '-0.0664', '-0.2534', '0.1031', '-0.505', '-0.07623', '0.1283', '-0.2367', '-0.17', '-0.02002', '0.2203', '0.2573', '-0.0856', '-0.009766', '-0.2025', '0.1837', '-0.0449', '-0.2417', '-0.576', '0.2495', '0.0767', '-0.1278', '0.06726', '0.2969', '-0.08746', '0.0328', '0.02963', '0.08307', '0.09174', '0.318', '0.1494', '-0.4045', '0.12006', '-0.2893', '-0.0584', '0.03497', '-0.2727', '-0.07837', '-0.01097', '-0.0263', '0.1927', '-0.189', '-0.1534', '-0.03824', '-0.012314', '-0.1437', '0.2394', '-0.05252', '-0.2112', '0.05438', '0.5244', '0.147', '0.1123', '-0.005573', '0.1898', '0.1606', '0.08386', '0.3962', '0.01107', '0.4602', '-0.48', '0.2837', '-0.006695']",,,C537608,,,,
mondo:0010824,disorder of sex development-intellectual disability syndrome,"['pseudohermaphroditism-intellectual disability syndrome', 'Verloes Gillerot Fryns syndrome', 'Verloes-Gillerot-Fryns syndrome', 'Verloes syndrome', 'disorder of sex development intellectual disability', 'male pseudohermaphroditism/mental retardation syndrome, Verloes type', 'Male pseudohermaphroditism intellectual disability syndrome, Verloes type', 'male pseudohermaphroditism/intellectual disability syndrome, Verloes type']",,600122,2983,,,,,C535693,,,,
mondo:0010825,atrioventricular defect-blepharophimosis-radial and anal defect syndrome,"['atrioventricular septal defect with blepharophimosis and anal and radial defects', 'Houlston-Ironton-Temple syndrome']",,600123,1352,C1838606,,,,C563994,,,,
mondo:0010826,childhood absence epilepsy,"['absence seizure', 'pyknolepsy', 'petit mal seizure']",1825,,64280,,"['1.012', '0.1609', '-0.4963', '-0.3152', '-0.4316', '-0.11646', '0.7944', '0.3562', '-0.4832', '-0.4607', '-0.1725', '-0.375', '-0.3152', '0.2133', '-0.03412', '-0.00633', '-0.506', '-0.5576', '-0.3418', '-0.3916', '-0.3562', '0.3674', '0.1389', '-0.588', '-0.263', '0.1646', '-0.2382', '-0.3787', '-0.57', '0.3083', '0.254', '-0.599', '0.435', '0.1636', '0.646', '0.2605', '-0.0211', '0.05408', '-0.11487', '-0.1279', '0.2185', '-0.422', '0.2908', '-0.488', '-0.2632', '-0.5664', '-0.1652', '0.222', '0.1497', '0.8623', '-0.0555', '0.1008', '-0.2693', '-0.4746', '0.1642', '-0.298', '-0.292', '0.06464', '-0.1696', '0.3542', '-0.748', '0.6143', '0.567', '-0.3196', '-0.2383', '1.279', '-0.1575', '-0.11816', '-0.5776', '0.4116', '0.762', '0.6187', '-0.2018', '-0.366', '0.614', '0.73', '0.753', '0.191', '-0.5205', '0.08105', '0.02142', '0.507', '0.3396', '0.11646', '0.5737', '0.1155', '0.2489', '0.773', '0.6', '0.515', '-0.10516', '0.347', '-0.323', '-0.02916', '0.1018', '0.3062', '0.2964', '-0.386', '0.389', '0.4138']",,,,,,,
mondo:0010827,retinitis pigmentosa 14,"['TULP1 retinitis pigmentosa', 'retinitis pigmentosa 14', 'retinitis pigmentosa caused by mutation in TULP1', 'retinitis pigmentosa type 14', 'RP14', 'RP 14']",0110381,600132,,C1838603,,,,,,H35.5,,
mondo:0010828,retinitis pigmentosa 11,"['retinitis pigmentosa 11', 'retinitis pigmentosa type 11', 'retinitis pigmentosa caused by mutation in PRPF31', 'RP11', 'PRPF31 retinitis pigmentosa', 'RP 11']",0110408,600138,,C1838601,,,,C563991,,H35.5,,
mondo:0010829,CARASIL syndrome,"['cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy', 'cerebral arteriopathy, autosomal recessive, with subcortical infarcts and leukoencephalopathy', 'CARASIL', 'Maeda syndrome', 'cerebrovascular disease with thin skin, alopecia, and disc disease', 'subcortical vascular encephalopathy, progressive', 'cerebrovascular disease with thin skin, alopecia, and disk disease']",,600142,199354,C1838577,"['0.036', '0.01724', '-0.0617', '-0.128', '-0.3604', '-0.00669', '0.0659', '0.256', '-0.575', '-0.2413', '-0.03748', '-0.194', '-0.3127', '0.333', '0.739', '-0.297', '0.578', '-0.11414', '-0.3801', '-0.2239', '-0.03253', '-0.3298', '-0.0568', '-0.889', '-0.2279', '-0.3809', '0.11835', '0.305', '0.2822', '0.3022', '0.473', '-0.4224', '0.377', '-0.4263', '0.5234', '-0.0002095', '-0.4355', '-0.641', '0.414', '0.1201', '0.4053', '-0.762', '0.194', '-0.2', '0.65', '0.5625', '-0.4675', '0.1975', '0.1819', '0.0756', '0.08093', '0.921', '-0.2627', '-0.11346', '0.3896', '0.2167', '0.585', '-0.5225', '-0.3728', '0.05936', '0.1838', '0.11395', '0.0352', '-0.3945', '-0.127', '0.2612', '0.2472', '0.734', '0.04507', '0.714', '-0.00876', '0.1002', '0.559', '-0.1443', '0.525', '0.6543', '0.615', '0.0312', '-0.3757', '-0.3328', '-0.03903', '-0.4563', '0.262', '0.5005', '-0.1355', '0.5337', '0.1724', '0.03888', '0.603', '0.07275', '0.486', '-0.3936', '-0.4067', '0.2686', '0.1276', '-0.1029', '0.757', '-0.07654', '-0.2874', '0.0856']",,,C563990,,,,
mondo:0010830,neuronal ceroid lipofuscinosis 8,"['CLN8 neuronal ceroid lipofuscinosis', 'CLN8 disease', 'ceroid lipofuscinosis, neuronal, 8', 'CLN8', 'ceroid lipofuscinosis, neuronal, type 8', 'neuronal ceroid lipofuscinosis caused by mutation in CLN8', 'neuronal ceroid lipofuscinosis type 8']",0110723,600143,228354,,"['-0.2683', '0.319', '-0.074', '0.1984', '0.0671', '-0.358', '-0.1438', '-0.0783', '-0.2183', '-0.00833', '-0.06506', '0.04626', '-0.08405', '-0.0414', '0.0995', '-0.2588', '-0.1278', '-0.1428', '-0.065', '-0.3496', '0.2113', '-0.2422', '0.1691', '-0.0948', '0.05344', '-0.045', '-0.00365', '-0.05453', '-0.2134', '0.07367', '0.1716', '0.10406', '0.2168', '0.0554', '0.3616', '0.0492', '-0.002531', '-0.162', '-0.03873', '-0.2312', '0.07886', '-0.3787', '0.1342', '0.0366', '-0.1746', '-0.476', '0.0738', '0.1514', '0.2202', '0.1917', '0.2322', '-0.0917', '-0.03763', '0.03137', '-0.06244', '-0.5576', '0.4827', '-0.0346', '-0.4883', '0.0772', '0.2083', '0.06903', '0.172', '0.013565', '0.05222', '0.07855', '0.416', '0.07465', '-0.202', '0.2202', '-0.2103', '-0.1185', '0.07166', '-0.1473', '0.146', '0.03009', '-0.05023', '0.1704', '-0.2074', '-0.0359', '0.0824', '-0.24', '-0.1217', '0.31', '-0.0323', '-0.4072', '0.2322', '0.2098', '0.0871', '0.1968', '0.2698', '-0.01485', '-0.02574', '-0.01312', '0.3088', '0.2158', '0.5293', '-0.3142', '-0.08276', '-0.0655']",,,C537952,,,,
mondo:0010831,familial caudal dysgenesis,"['caudal regression syndrome', 'sacral agenesis', 'familial caudal dysgenesis', 'SDAM', 'sirenomelia', 'caudal dysgenesis syndrome', 'Sdam', 'caudal dysgenesis familial type', 'sacral defect with anterior meningocele', 'Rudd-Klimek syndrome', 'caudal regression']",,600145,1768,,"['-0.1514', '-0.148', '0.2054', '-0.1432', '0.09375', '-0.1619', '0.1525', '0.2517', '-0.2659', '-0.2812', '-0.4045', '-0.3186', '0.1061', '0.2827', '-0.5854', '0.06335', '0.2', '-0.1287', '-0.07385', '-0.1904', '0.3706', '0.279', '0.7275', '-0.2045', '0.0941', '0.04294', '0.1835', '0.637', '0.7476', '-0.1417', '0.799', '0.0459', '0.3552', '0.3174', '0.2103', '-0.6377', '0.0475', '-0.3694', '-0.4417', '-0.4006', '0.3196', '0.04126', '-0.007465', '-0.1616', '-0.1864', '-0.1367', '0.2113', '0.4172', '-0.2737', '0.0718', '-0.2856', '-0.3445', '-0.1833', '0.01506', '-0.7563', '-0.2129', '-0.1416', '0.03812', '-0.2114', '0.07416', '-0.2383', '-0.2163', '-0.2734', '0.128', '-0.3103', '0.4136', '0.803', '0.3137', '-0.4868', '-0.0919', '-0.06134', '-0.09174', '0.1266', '-0.1803', '-0.2241', '0.316', '0.4836', '0.1558', '-0.577', '-0.4312', '-0.546', '-0.01318', '0.3079', '0.3623', '0.0863', '-0.1556', '0.0626', '-0.0115', '0.0844', '-0.606', '-0.1671', '0.3906', '0.655', '0.3743', '0.7637', '-0.2612', '0.406', '-0.279', '-0.0808', '0.10236']",C99054,,,,,,
mondo:0010832,Bardet-Biedl syndrome 3,"['BBS3', 'Bardet-Biedl syndrome type 3', 'Bardet-Biedl syndrome 3']",0110125,600151,,C1859564,,,,C537911,,,,
mondo:0010833,"Hirschsprung disease, susceptibility to, 2","['Hirschsprung disease caused by mutation in EDNRB', 'EDNRB Hirschsprung disease', 'HSCR2', 'Hirschsprung disease type 2', 'Hirschsprung disease, susceptibility to, 2', 'susceptibility to Hirschsprung disease 2', 'Hirschsprung disease, susceptibility to, type 2']",,600155,,,,,,,,,,
mondo:0010834,"Hirschsprung disease, susceptibility to, 5","['HSCR5', 'Hirschsprung disease, susceptibility to, 5']",,600156,,,,,,,,,,
mondo:0010835,pterygium colli-intellectual disability-digital anomalies syndrome,"['pterygium colli and intellectual disability with facial and digital anomalies', 'khalifa-Graham syndrome', 'pterygium colli mental retardation digital anomalies', 'pterygium colli and mental retardation with facial and digital anomalies', 'pterygium colli intellectual disability digital anomalies']",,600159,2988,C1838562,,,,C535831,,,,
mondo:0010836,nanophthalmos 1,"['Nanophthalmia 1', 'nanophthalmos with high hyperopia and angle-closure glaucoma', 'nanophthalmos, autosomal dominant', 'NNO1', 'nanophthalmos-1', 'microphthalmos, simple, autosomal dominant', 'nanophthalmos 1']",,600165,,C1838502,,,,C563983,,,,
mondo:0010837,primary hyperparathyroidism,"['primary hyperparathyroidism', 'primary hyperparathyroidism (disease)']",11202,,99878,,,C48280,0008519,D049950,252.01,,,0008200
mondo:0010838,gonadal agenesis,['gonadal agenesis'],,600171,,,,C27228,,,,,,
mondo:0010839,autosomal dominant congenital benign spinal muscular atrophy,"['HMN8', 'autosomal dominant benign distal spinal muscular atrophy', 'congenital benign spinal muscular atrophy with contractures', 'spinal muscular atrophy, distal, congenital nonprogressive', 'congenital nonprogressive spinal muscular atrophy', 'neuropathy, distal hereditary motor, type 8', 'neuronopathy, distal hereditary motor, type 8', 'spinal muscular atrophy, congenital benign, with contractures', 'neuronopathy, distal hereditary motor, type VIII']",0111215,600175,1216,C1838492,"['-0.7886', '-0.0429', '0.2333', '-0.4224', '0.1393', '-0.4958', '-0.1067', '0.6436', '-0.9595', '0.1277', '-0.03568', '-0.1039', '-0.3943', '0.1371', '0.1282', '0.3262', '0.2457', '-0.409', '-0.2188', '-0.836', '0.3345', '-0.1652', '0.2252', '0.183', '-0.0146', '0.2595', '0.1998', '-0.2227', '-0.2125', '-0.2656', '0.0522', '-0.1544', '0.1553', '0.547', '-0.0763', '-0.4226', '-0.166', '-0.0997', '-0.0538', '-0.1984', '-0.1948', '-0.3967', '-0.4731', '0.685', '0.0542', '-0.3066', '-0.279', '0.53', '0.2632', '0.707', '-0.1478', '0.507', '0.0666', '-0.3245', '-0.3467', '-0.4854', '0.2861', '-0.08124', '-0.2788', '-0.1469', '0.2676', '0.1747', '-0.235', '0.3477', '-0.6885', '0.1652', '0.3152', '0.8735', '-0.1865', '0.03253', '-0.491', '0.1937', '0.1694', '-0.438', '0.566', '-0.1768', '0.139', '0.3691', '-0.269', '-0.4253', '-0.3271', '-0.279', '0.7544', '0.649', '-0.308', '0.388', '-0.2015', '0.11707', '0.04816', '-0.0461', '0.06323', '0.4333', '0.3303', '0.1526', '0.4822', '0.0943', '1.032', '0.1536', '-0.0765', '0.503']",,,C563981,,,,
mondo:0010840,pachygyria-intellectual disability-epilepsy syndrome,"['pachygyria, mental retardation and epilepsy', 'Kuzniecky syndrome', 'pachygyria with mental retardation, seizures, and arachnoid cysts', 'pachygyria with mental retardation and seizures', 'pachygyria with intellectual disability, seizures, and arachnoid cysts', 'pachygyria, intellectual disability and epilepsy', 'pachygyria with intellectual disability and seizures']",,600176,2798,C1838491,,,,C538091,,,,
mondo:0010841,Waardenburg syndrome type 2B,"['Waardenburg syndrome, type 2B', 'Waardenburg syndrome type IIB', 'WS2B']",0110947,600193,,C1838447,,,,C536465,,,,
mondo:0010842,multiple cutaneous and mucosal venous malformations,"['VENOUS malformations, multiple cutaneous and mucosal', 'Vmcm1', 'cutaneous and mucosal venous malformation', 'VMCM', 'mucocutaneous venous malformations']",0050792,600195,2451,,"['0.0783', '-0.1692', '-0.813', '-0.1661', '0.384', '0.131', '0.1906', '-0.1667', '-0.4778', '-0.252', '-0.2335', '0.1865', '0.4854', '0.0768', '0.0407', '0.4775', '0.3457', '-0.0672', '-0.1917', '-0.4817', '-0.0918', '-0.1234', '0.775', '-0.3447', '-0.06146', '-0.11566', '-0.0634', '0.2014', '0.4116', '-0.1908', '0.9478', '-0.4973', '-0.0852', '-0.0452', '-0.2747', '-0.152', '-0.1105', '-0.4294', '0.371', '-0.1456', '0.626', '-0.4578', '0.5024', '-0.4785', '0.1603', '0.0867', '-0.3652', '0.09015', '-0.0745', '-0.0553', '-0.05905', '-0.1282', '-0.06775', '0.4258', '-0.5713', '0.4438', '0.378', '0.07294', '-0.826', '0.2683', '0.1809', '0.391', '-0.1659', '-0.3137', '-0.04272', '0.2161', '0.2219', '0.867', '-0.04922', '0.145', '-0.01414', '-0.0967', '-0.2876', '-0.1511', '0.4263', '-0.0595', '0.2014', '-0.418', '0.141', '-0.9106', '-0.617', '0.4163', '-0.1656', '0.1052', '-0.4065', '0.1316', '0.02448', '0.1533', '-0.1151', '-0.1119', '-0.1356', '0.2344', '-0.1954', '-0.0679', '0.7915', '-0.3362', '0.54', '-0.668', '-0.0826', '-0.1727']",,,C563977,,,,
mondo:0010843,"dyslexia, susceptibility to, 2","['DYX2', 'reading disability, specific, 2', 'dyslexia, susceptibility to, 2']",,600202,,,,,,,,,,
mondo:0010844,"epiphyseal dysplasia, multiple, 2","['epiphyseal dysplasia, multiple, type 2', 'epiphyseal dysplasia multiple 2', 'multiple epiphyseal dysplasia 2', 'EDM2', 'epiphyseal dysplasia, multiple, 2', 'COL9A2 multiple epiphyseal dysplasia (disease)']",0070298,600204,,C1838429,,,,C535502,,,,
mondo:0010846,"exostoses, multiple, type III","['exostoses, multiple, type III', 'exostoses, multiple, type 3', 'EXT3']",,600209,,C1838420,,,,C563975,,,,
mondo:0010847,spinocerebellar ataxia type 4,"['spinocerebellar ataxia 4', 'spinocerebellar ataxia autosomal dominant with sensory axonal neuropathy', 'SCA4', 'spinocerebellar ataxia, autosomal dominant, with sensory axonal neuropathy']",0050957,600223,98765,C0752122,,,,,,,,
mondo:0010848,spinocerebellar ataxia type 5,"['SCA5', 'spinocerebellar ataxia 5', 'spinocerebellar ataxia type 5']",0050882,600224,98766,C0752123,"['0.005848', '-0.2277', '-0.02232', '0.2013', '0.07355', '-0.6196', '0.1556', '0.684', '-0.465', '-0.8164', '0.2427', '0.2003', '0.0749', '-0.05545', '0.6304', '-0.1924', '-0.1952', '-0.577', '0.12024', '-0.776', '-0.2537', '-0.005108', '-0.1511', '-0.2703', '-0.1368', '-0.542', '-0.4211', '0.1077', '0.1875', '-0.6797', '0.1274', '0.663', '-0.1565', '-0.0982', '0.2925', '-0.2847', '0.0875', '0.01202', '0.2795', '0.3503', '0.562', '0.2452', '-0.2228', '0.4026', '0.4922', '-0.4822', '-0.2081', '0.1903', '0.1293', '-0.4485', '-0.1149', '0.2177', '-0.1766', '-0.742', '-0.01994', '-0.631', '0.4756', '0.2153', '-0.1761', '0.5703', '-0.454', '0.5405', '0.2008', '-0.3174', '-0.4514', '0.2335', '0.3616', '0.3684', '-0.5635', '0.532', '0.5566', '0.1868', '-0.322', '-0.5205', '0.8438', '0.2751', '0.2996', '-0.05344', '0.0313', '0.549', '0.1825', '-0.785', '0.856', '0.806', '-0.515', '-0.3914', '0.0378', '0.1914', '0.5894', '0.5264', '0.414', '0.2817', '0.01386', '-0.02028', '0.881', '0.906', '0.4353', '0.687', '-0.2334', '0.1498']",,,,,,,
mondo:0010849,"palmoplantar keratoderma, Bothnian type","['PPKB', 'palmoplantar keratoderma, Bothnian type']",0111707,600231,2337,,"['-0.04236', '0.11285', '-0.01414', '-0.03265', '0.03836', '-0.1375', '-0.02902', '0.03302', '-0.04053', '-0.01743', '-0.0366', '-0.02315', '-0.03827', '-0.03656', '-0.05893', '-0.004086', '0.04898', '-0.11896', '-0.01036', '-0.2566', '-0.047', '0.00367', '0.111', '-0.02097', '0.0709', '0.03497', '-0.02759', '0.04126', '-0.04126', '-0.0749', '0.0719', '-0.02174', '0.0644', '0.03467', '0.03204', '-0.01034', '-0.01729', '-0.0326', '-0.01765', '-0.0609', '0.002195', '-0.0964', '0.0158', '-0.01562', '0.000498', '-0.06946', '-0.0715', '0.1049', '-0.007626', '-0.01701', '-0.08124', '-0.02528', '0.06085', '0.01855', '-0.0751', '-0.0634', '0.1482', '-0.0615', '-0.1665', '-0.04266', '0.08215', '0.02013', '-0.0235', '-0.03732', '0.02188', '0.014114', '0.1256', '0.09863', '-0.01035', '0.1582', '-0.1427', '-0.001831', '0.05392', '-0.0316', '0.0577', '0.00817', '0.02307', '-0.0353', '-0.0189', '-0.0658', '0.003372', '0.02484', '0.01942', '0.05298', '0.01779', '-0.02736', '-0.01717', '0.138', '0.1465', '0.0588', '0.0362', '0.0977', '0.06012', '0.062', '0.1548', '-0.000777', '0.1251', '-0.1156', '0.006317', '0.03036']",,,,,,,
mondo:0010850,Tessier number 4 facial cleft,"['facial clefting, oblique, 1', 'oculomaxillofacial dysplasia with oblique Facial clefts', 'OBLFC1', 'facial clefting, oblique, type 1']",0111706,600251,141258,,"['-0.0106', '0.2546', '0.2429', '-0.12305', '-0.04987', '-0.1567', '0.3015', '0.4385', '-0.4985', '-0.04764', '-0.1703', '0.03625', '-0.04694', '-0.00563', '-0.0922', '-0.08295', '0.2', '-0.326', '-0.2695', '-0.488', '-0.0579', '0.3025', '0.2166', '-0.1038', '0.2578', '-0.11206', '-0.1003', '-0.01396', '0.0812', '-0.215', '0.1731', '-0.096', '0.1846', '0.2788', '0.259', '-0.04276', '0.1871', '-0.1559', '-0.0944', '-0.4026', '0.3228', '0.005856', '-0.2654', '-0.3955', '-0.3423', '0.08594', '0.02686', '0.3264', '-0.1615', '-0.1405', '-0.3752', '0.06537', '-0.2656', '-0.0642', '-0.3906', '-0.6016', '-0.07056', '0.0962', '-0.2191', '-0.1611', '0.2568', '0.343', '-0.3064', '0.3289', '-0.2291', '0.01617', '0.3801', '0.1832', '-0.169', '-0.07104', '-0.2386', '0.443', '0.2091', '-0.1586', '-0.1315', '-0.0451', '0.03928', '-0.279', '-0.3162', '-0.03668', '-0.2712', '-0.142', '0.3447', '0.8403', '-0.13', '-0.2048', '-0.3203', '0.3904', '0.1367', '0.2727', '0.00819', '0.3525', '0.04895', '0.1725', '0.673', '-0.3262', '0.5073', '-0.3474', '0.3503', '0.1659']",,,,,,,
mondo:0010851,Lowry-MacLean syndrome,"['Lowry-MacLean syndrome', 'intellectual disability, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, craniosynostosis and growth failure', 'mental retardation, cleft palate, eventration of diaphragm, congenital heart defect, glaucoma, craniosynostosis and growth failure', 'Lowry MacLean syndrome']",,600252,2409,C0796020,,,,C537037,,,,
mondo:0010852,chromosome 8Q12.1-q21.2 deletion syndrome,"['bor-Duane hydrocephalus contiguous Gene syndrome', 'chromosome 8Q12.1-q21.2 deletion syndrome', 'Branchio-Oto-renal Duane hydrocephalus contiguous gene syndrome']",,600257,,C1838346,,,,C536574,,,,
mondo:0010853,"Helicobacter pylori infection, susceptibility to","['Helicobacter pylori infection, susceptibility to', 'H. pylori infection, susceptibility to']",,600263,,C1838332,,,,,,,,
mondo:0010854,Toriello-Lacassie-Droste syndrome,"['oculoectodermal syndrome', 'aplasia cutis congenita with epibulbar dermoids', 'oes', 'aplasia cutis congenita-epibulbar dermoids syndrome', 'Toriello Lacassie Droste syndrome', 'oculoectodermal syndrome, somatic', 'oculo-ectodermal syndrome']",0111705,600268,3339,C1838329,"['-0.0899', '0.10974', '0.1438', '-0.29', '0.1687', '-0.3188', '-0.0563', '0.1692', '-0.2976', '-0.1823', '-0.2118', '0.01336', '-0.03403', '-0.02731', '-0.1707', '-0.038', '0.1995', '-0.0205', '-0.1217', '-0.517', '-0.04666', '-0.003466', '0.2637', '-0.0942', '0.078', '0.1271', '-0.258', '-0.0707', '0.2961', '-0.3032', '0.2966', '0.1779', '0.1715', '0.1783', '0.1033', '-0.2593', '-0.0006623', '-0.2048', '-0.08954', '-0.3162', '-0.03195', '-0.333', '0.011665', '-0.1929', '-0.04196', '-0.2147', '-0.04272', '0.2927', '0.1361', '-0.1151', '-0.1455', '-0.0421', '0.1221', '-0.1497', '-0.421', '-0.163', '0.05573', '-0.06604', '-0.3486', '-0.0699', '0.1483', '0.0694', '0.05798', '-0.05505', '-0.004887', '-0.1163', '0.2656', '0.1637', '-0.3293', '0.1719', '-0.385', '0.0634', '0.08875', '-0.0782', '0.2023', '-0.0715', '-0.01723', '0.0505', '-0.1545', '-0.2651', '-0.006668', '0.01952', '-0.02698', '0.2222', '-0.0642', '-0.1481', '0.03558', '0.4485', '0.09265', '-0.1074', '0.2095', '0.3582', '0.1876', '-0.0865', '0.373', '-0.1533', '0.349', '-0.5347', '0.188', '0.1554']",,,C563969,,,,
mondo:0010855,short tarsus-absence of lower eyelashes syndrome,"['Lopes Gorlin syndrome', 'short tarsus with absence of LOWER eyelashes', 'stale', 'Lopes-Gorlin syndrome', 'short tarsus absence of lower eyelashes']",,600269,2832,C1838328,,,,C537036,,,,
mondo:0010856,autosomal dominant polycystic kidney disease type 1 with tuberous sclerosis,"['polycystic kidney disease, infantile severe, with tuberous sclerosis', 'chromosome 16P13.3 deletion syndrome, distal', 'PKDTS', 'tuberous sclerosis polycystic kidney disease contiguous gene syndrome', 'polycystic kidneys, severe infantile with tuberous sclerosis', 'tuberous sclerosis/polycystic kidney disease contiguous gene syndrome']",,600273,88924,C1838327,,,,C536328,,,,
mondo:0010857,semantic dementia,"['frontotemporal dementia', 'Pallidopontonigral Degeneration', 'Ftdp17', 'frontotemporal dementia with Parkinsonism', 'dementia, frontotemporal, with or without parkinsonism', 'frontotemporal lobe dementia', 'dementia, frontotemporal, with Parkinsonism', 'FTD', 'Ftld with Tau inclusions', 'dementia, frontotemporal', 'semantic variant PPA', 'frontotemporal lobar Degeneration with Tau inclusions', 'semantic primary progressive aphasia', 'multiple system tauopathy with presenile dementia', 'Wilhelmsen-Lynch disease', 'Pick Complex', 'disinhibition-dementia-Parkinsonism-amyotrophy Complex']",,600274,100069,C1862937,"['0.18', '-0.1482', '-0.0631', '-0.3853', '-0.3489', '-0.149', '-0.082', '0.0679', '-1.129', '-0.4553', '-0.096', '-0.4521', '0.1616', '0.5864', '0.4573', '-0.908', '-0.2202', '-0.338', '-0.4119', '0.2104', '0.393', '-0.1377', '-0.1693', '0.04593', '0.924', '-0.1257', '-0.2272', '-0.02202', '-0.125', '-0.1893', '0.2375', '-0.0755', '-0.03415', '-0.427', '0.773', '-0.3997', '-0.4717', '-0.3108', '0.2537', '-1.152', '0.949', '-0.666', '0.3093', '-0.1615', '0.1987', '0.002066', '0.467', '-0.345', '0.3774', '0.3398', '0.3423', '0.1129', '0.2705', '-0.579', '0.1476', '0.267', '-0.0185', '-0.551', '-0.535', '-0.6147', '-0.0483', '0.376', '0.2979', '-0.815', '0.0864', '0.6978', '0.4026', '0.9546', '-0.7305', '0.8677', '0.2727', '-0.05853', '0.11884', '0.10236', '-0.432', '0.8765', '0.1373', '0.3352', '-0.97', '-0.1371', '-0.2223', '-0.656', '-0.4795', '1.096', '0.693', '0.509', '-0.1631', '-0.1473', '1.587', '1.0205', '0.191', '0.616', '-0.1456', '0.904', '-0.5137', '0.3835', '-0.333', '0.05768', '-0.494', '-0.4412']",,,,,,,
mondo:0010858,macrocephaly-spastic paraplegia-dysmorphism syndrome,"['macrocephaly with spastic paraplegia and distinctive craniofacial appearance', 'Fryns macrocephaly']",,600302,2429,C1838281,,,,C563963,,,,
mondo:0010860,autosomal recessive nonsyndromic hearing loss 3,"['deafness, autosomal recessive 3', 'deafness, autosomal recessive type 3', 'NRSD3', 'autosomal recessive nonsyndromic deafness 3', 'DFNB3', 'neurosensory nonsyndromic recessive deafness 3', 'autosomal recessive nonsyndromic deafness caused by mutation in MYO15A', 'autosomal recessive nonsyndromic deafness type 3', 'autosomal recessive deafness 3, neurosensory nonsyndromic recessive deafness 3', 'MYO15A autosomal recessive nonsyndromic deafness']",0110488,600316,,C1838263,,,,C563961,,,,
mondo:0010861,type 1 diabetes mellitus 3,"['IDDM3', 'diabetes mellitus, insulin-dependent, 3', 'insulin-dependent diabetes mellitus 3']",0110742,600318,,C1838262,,,,C563960,,,,
mondo:0010862,type 1 diabetes mellitus 4,"['insulin-dependent diabetes mellitus 4', 'diabetes mellitus, insulin-dependent, 4', 'IDDM4']",0110743,600319,,C1838261,,,,C563959,,,,
mondo:0010863,type 1 diabetes mellitus 5,"['insulin-dependent diabetes mellitus 5', 'type 1 diabetes mellitus caused by mutation in SUMO4', 'diabetes mellitus, insulin-dependent, 5', 'IDDM5', 'SUMO4 type 1 diabetes mellitus', 'diabetes mellitus, insulin-dependent, type 5']",0110744,600320,,C1838260,,,,C563958,,,,
mondo:0010864,type 1 diabetes mellitus 7,"['insulin-dependent diabetes mellitus 7', 'IDDM7', 'diabetes mellitus, insulin-dependent, 7']",0110746,600321,,C1838259,,,,C563957,,,,
mondo:0010865,pseudoaminopterin syndrome,"['aminopterin syndrome sine aminopterin', 'ASSA', 'aminopterin syndrome-like sine aminopterin', 'pseudoaminopterin syndrome']",,600325,221120,C0795939,,,,C535823,,Q82.0,,
mondo:0010866,infantile osteopetrosis with neuroaxonal dysplasia,['osteopetrosis and infantile neuroaxonal dystrophy'],0070343,600329,85179,C1838258,"['-0.09753', '0.3767', '0.08374', '-0.1289', '0.475', '-0.4126', '-0.3755', '0.879', '-0.02017', '-0.278', '-0.2783', '-0.3965', '-0.2566', '-0.686', '0.3726', '-0.04337', '0.3215', '-0.09143', '-0.2634', '-0.3186', '0.04376', '-0.0962', '0.5464', '-0.2075', '-0.10913', '0.01005', '0.12494', '0.02725', '-0.33', '-0.1951', '0.638', '-0.214', '0.3513', '-0.131', '-0.02477', '0.3938', '-0.02576', '-0.3677', '-0.06836', '-0.1827', '0.1731', '-0.2617', '-0.3066', '-0.277', '-0.1599', '-0.03006', '0.03882', '0.2717', '-0.1709', '-0.4663', '0.4175', '-0.2817', '-0.1465', '0.12427', '-0.1718', '-0.4163', '-0.0546', '0.02682', '-0.293', '0.4292', '0.494', '-0.1997', '0.07263', '-0.1661', '-0.143', '-0.2085', '0.292', '0.4753', '-0.727', '0.0951', '0.7036', '0.231', '-0.0658', '-0.2021', '0.11725', '0.1324', '-0.1799', '0.4011', '0.01278', '-0.1981', '-0.08057', '0.1236', '0.128', '0.4763', '-0.26', '-0.1979', '0.1924', '0.358', '0.01915', '-0.0854', '-0.04843', '-0.06238', '-0.1172', '0.06635', '0.5317', '0.1575', '0.543', '-0.3047', '-0.1975', '-0.2008']",,,C536055,,,,
mondo:0010867,PARC syndrome,"['poikiloderma-alopecia-retrognathism-cleft palate syndrome', 'PARC syndrome', 'poikiloderma, alopecia, retrognathism, and cleft palate']",,600331,2825,C1838256,,,,C537174,,,,
mondo:0010868,rippling muscle disease 1,"['rippling muscle disease, 1', 'rippling muscle disease 1', 'RMD1', 'rippling muscle disease-1']",0070308,600332,,,,,,,,,,
mondo:0010869,motor neuron disease with dementia and ophthalmoplegia,['motor neuron disease with dementia and ophthalmoplegia'],,600333,,C1838253,,,,C563954,,,,
mondo:0010870,tibial muscular dystrophy,"['Finnish tibial muscular dystrophy', 'tardive tibial muscular dystrophy', 'distal titinopathy', 'TMD', 'distal myopathy, Udd type', 'Udd myopathy', 'Tmd', 'Udd type distal myopathy', 'tibial muscular dystrophy, tardive']",0111078,600334,609,C1838244,,,,,,,,
mondo:0010871,succinic acidemia,['succinic acidemia'],,600335,936,C1838243,,,,C563952,,,,
mondo:0010872,"parotid salivary glands, polycystic dysgenetic disease of","['parotid salivary glands, polycystic dysgenetic disease OF', 'PDDP']",,600343,,,,,,,,,,
mondo:0010873,band heterotopia of brain,"['band heterotopia of brain', 'band heterotopia', 'BH']",,600348,,C1838239,,,,C563950,,,,
mondo:0010874,"enteropathy, familial, with villous edema and immunoglobulin G2 deficiency","['enteropathy, familial, with villous edema and immunoglobulin G2 deficiency']",,600351,,C1838238,,,,C563949,,,,
mondo:0010875,"pachydermodactyly, familial","['pachydermodactyly, familial']",,600356,,C1838218,,,,C563947,,,,
mondo:0010876,recessive aplasia cutis congenita of limbs,"['aplasia cutis congenita of limbs recessive', 'recessive aplasia cutis congenita of the limbs', 'aplasia cutis congenita of limbs, autosomal recessive', 'congenital absence of skin on the upper or lower limbs']",,600360,1115,C1838206,,,,C536840,,,,
mondo:0010877,Charcot-Marie-Tooth disease type 5,"['CMT with pyramidal features', 'hereditary motor and sensory neuropathy V', 'HMSN 5', 'HMSN5', 'Charcot-Marie-Tooth neuropathy with pyramidal features, autosomal dominant', 'hereditary motor and sensory neuropathy type 5', 'hereditary motor and sensory neuropathy 5', 'peroneal muscular atrophy with pyramidal features, autosomal dominant', 'hereditary motor and sensory neuropathy with pyramidal features', 'Charcot-Marie-Tooth disease-pyramidal features syndrome', 'Charcot-Marie-Tooth disease with pyramidal features, autosomal dominant']",0080067,600361,64751,CN074211,,,,,,,,
mondo:0010878,hereditary spastic paraplegia 6,"['familial spastic paraplegia autosomal dominant 3', 'SPG6', 'hereditary spastic paraplegia type 6', 'spastic paraplegia 6, autosomal dominant', 'hereditary spastic paraplegia caused by mutation in NIPA1', 'autosomal dominant familial spastic paraplegia type 3', 'familial spastic paraplegia, autosomal dominant, 3', 'autosomal dominant spastic paraplegia type 6', 'spastic paraplegia 6', 'NIPA1 hereditary spastic paraplegia', 'autosomal dominant spastic paraplegia 6', 'FSP3']",0110811,600363,100988,C4518537,"['0.1622', '0.3733', '0.1362', '-0.4102', '-0.1282', '-0.8926', '-0.3396', '-0.07465', '-0.872', '-0.3677', '-0.2908', '0.1118', '-0.2527', '0.1725', '0.4949', '-0.1713', '-0.2764', '-0.572', '0.3186', '-0.3848', '0.08234', '-0.1471', '-0.01214', '0.05753', '0.03128', '0.1448', '-0.2373', '-0.0832', '-0.1805', '-0.2195', '0.0794', '-0.1187', '-0.0692', '0.378', '-0.1421', '-0.3635', '-0.4158', '-0.3213', '-0.2222', '-0.2214', '0.5894', '-0.444', '0.073', '0.1982', '0.0338', '-0.6455', '-0.479', '-0.08', '-0.357', '0.2876', '0.171', '0.847', '-0.31', '-0.2732', '0.4062', '-0.1993', '0.5186', '-0.2505', '-0.2334', '-0.10034', '-0.3367', '0.2278', '0.379', '0.3496', '-0.03357', '0.572', '0.6123', '0.6895', '-0.2085', '0.3618', '-0.3118', '0.5415', '0.3274', '-0.0833', '0.451', '-0.0005608', '-0.0088', '0.2524', '0.326', '-0.4634', '-0.1494', '-0.10114', '0.53', '0.614', '0.2476', '0.1648', '-0.0714', '0.1222', '0.4136', '-0.01978', '0.2847', '0.234', '0.04803', '0.12354', '0.801', '0.3965', '0.5293', '-0.01657', '0.327', '0.3586']",,,C536866,,,,
mondo:0010879,CODAS syndrome,"['cerebral, ocular, dental, auricular, and skeletal anomalies syndrome', 'cerebral, ocular, dental, auricular, and skeletal syndrome', 'cerebrooculodentoauriculoskeletal syndrome', 'CODAS syndrome', 'cerebro-oculo-dento-auriculo-skeletal syndrome']",0111274,600373,1458,C1838180,"['0.2002', '0.02669', '0.5166', '0.2024', '0.4487', '0.03894', '-0.5347', '1.014', '-0.343', '0.3206', '-0.2216', '-0.539', '-0.0913', '-0.322', '-0.1821', '0.2798', '0.0581', '-0.2822', '-0.7495', '-0.4321', '0.0392', '-0.0921', '0.4443', '-0.2025', '0.0849', '-0.3433', '-1.148', '0.1305', '0.592', '-0.5547', '0.5244', '-0.0339', '0.3052', '-0.05405', '-0.0912', '-0.1209', '-0.2234', '-0.4749', '-0.627', '-0.729', '0.05887', '-0.2164', '-0.04614', '-0.5903', '0.1289', '-0.3364', '-0.04776', '0.3684', '-0.2385', '-0.2776', '-0.01468', '0.01255', '0.0435', '0.1941', '-0.4304', '-0.7695', '-0.04', '-0.1942', '-0.332', '-0.06125', '0.3052', '-0.052', '-0.2783', '0.5312', '0.09735', '-0.3428', '0.228', '0.4653', '-0.3738', '0.01338', '-0.4824', '0.11707', '-0.06525', '-0.3494', '-0.09216', '-0.2554', '-0.2625', '0.1882', '0.0362', '0.1433', '0.631', '-0.05743', '-0.05084', '1.237', '-0.4563', '0.0882', '-0.1471', '0.459', '0.1707', '0.161', '-0.2297', '0.5796', '0.1713', '0.508', '0.4507', '-0.2228', '0.1296', '-0.517', '0.735', '0.316']",C126744,,C536434,,,,
mondo:0010880,"telangiectasia, hereditary hemorrhagic, type 2","['pulmonary arterial hypertension, hereditary hemorrhagic telangiectasia-related', 'HHT2', 'telangiectasia, hereditary hemorrhagic, type 2', 'ORW2', 'Osler Weber Rendu syndrome type 2', 'ACVRL1 hereditary hemorrhagic telangiectasia', 'hereditary hemorrhagic telangiectasia type 2', 'telangiectasia hereditary hemorrhagic type 2', 'hereditary hemorrhagic telangiectasia caused by mutation in ACVRL1']",,600376,,,,,,,,,,
mondo:0010881,mesomelia-synostoses syndrome,"['dominant mesomelic shortness of stature with acral synostoses, umbilical anomalies, and soft palate agenesis', 'mesomelia-synostoses syndrome, Verloes-David-Pfeiffer type', 'mesomelia-synostoses syndrome', 'mesomelic dysplasia with acral synostoses, Verloes-David-Pfeiffer type', 'mesomelic dysplasia, syndromic', 'monosomy 8q13', 'chromosome 8Q13 deletion syndrome', 'Verloes-David syndrome', 'mesomelia synostoses', '8q13 microdeletion syndrome', 'Del(8)q(13)']",,600383,2496,C1838162,,,,C537348,,,,
mondo:0010882,aphalangy-syndactyly-microcephaly syndrome,"['Aphalangia, partial, with syndactyly and Duplication of metatarsal 4', 'APHALANGIA, partial, with syndactyly and DUPLICATION of metatarsal IV', 'Aphalangia, partial, with syndactyly and Duplication of metatarsal type 4', 'Aphalangia partial with syndactyly and duplication of metatarsal IV']",,600384,1113,C1838161,,,,C563942,,,,
mondo:0010883,pectus excavatum-macrocephaly-dysplastic nails syndrome,"['pectus excavatum, macrocephaly and dysplastic nails', 'Zori-Stalker-Williams syndrome', 'familial short stature, developmental delay, pectus abnormalities, distinctive facies, and dysplastic nails', 'Zori Stalker Williams syndrome', 'pectus excavatum, macrocephaly, short stature, and dysplastic nails']",,600399,2835,C2931302,,,,C536728,,,,
mondo:0010884,"muscular dystrophy, scapulohumeral","['muscular dystrophy, scapulohumeral']",,600416,,C0410192,,,,C562932,,,,
mondo:0010885,angiokeratoma corporis diffusum with arteriovenous fistulas,['angiokeratoma corporis diffusum with arteriovenous fistulas'],,600419,,C1838141,,,,C563940,,,,
mondo:0010886,2q37 microdeletion syndrome,"['Albright hereditary osteodystrophy type 3', 'brachydactyly-mental retardation syndrome', 'chromosome 2q37 deletion syndrome', 'brachydactyly-intellectual disability syndrome', 'deletion 2q37-qter', '2q37 monosomy', 'brachydactyly intellectual disability syndrome', 'deletion 2q37', 'monosomy 2q37-qter', '2q37 deletion syndrome', 'Del(2)(q37)', 'brachydactyly mental retardation syndrome', 'Albright hereditary osteodystrophy-like syndrome', 'BDMR']",0111704,600430,1001,C2931817,"['0.10406', '0.333', '-0.03403', '-0.1766', '0.2172', '-0.2673', '0.509', '0.3945', '-0.74', '-0.3572', '0.2644', '-0.3713', '0.7017', '-0.3237', '0.04584', '0.153', '0.446', '-0.1478', '-0.8003', '-0.03008', '0.1981', '0.0817', '0.3218', '-0.23', '0.519', '-0.1378', '-0.092', '0.1605', '0.2412', '-0.374', '0.607', '-0.1451', '0.816', '0.1295', '0.003305', '-0.137', '-0.6772', '-0.506', '-0.53', '-0.2747', '0.4111', '-0.03214', '0.05746', '-0.1997', '0.632', '-0.4272', '0.072', '0.6553', '-0.12396', '0.1166', '-0.654', '0.1141', '-1.017', '0.198', '-0.3206', '-0.09186', '-0.1693', '0.383', '0.1664', '-0.7476', '-0.04953', '0.2617', '-0.11017', '0.1831', '0.004234', '0.02963', '0.3044', '0.1864', '-0.4775', '0.1606', '0.03058', '0.0808', '-0.002327', '-0.01912', '0.4478', '-0.00802', '0.3518', '-0.677', '-0.2052', '0.1355', '0.1387', '-0.3467', '-0.04095', '0.3762', '0.344', '0.4072', '-0.1395', '0.598', '0.2113', '0.2703', '-0.2834', '0.604', '-0.1373', '0.258', '0.6562', '-0.469', '0.2172', '-0.481', '0.58', '0.268']",C129021,,C538317,758.39,,,
mondo:0010887,isolated anterior cervical hypertrichosis,"['Tsukahara Kajii syndrome', 'anterior cervical hypertrichosis', 'hairy throat syndrome', 'hypertrichosis, anterior cervical', 'Tsukahara-Kajii syndrome', 'hairy throat']",,600457,3387,C1838123,,,,C538390,,,,
mondo:0010888,adenomyosis,"['uterine corpus adenomyosis', 'endometriosis interna', 'uterus corpus adenomyosis', 'adenomyosis of uterus', 'uterine adenomyosis', 'adenomyosis of the uterus', 'myometrium endometriosis (disease)', 'endometriosis of uterus', 'endometriosis of myometrium', 'endometriosis, myometrium']",288,600458,,C0341858,,C6996,1001757,D062788,617.0,N80.0,,
mondo:0010889,arterial dissection-lentiginosis syndrome,['arterial dissection with lentiginosis'],,600459,1682,C1838122,,,,C563937,,,,
mondo:0010890,acrocardiofacial syndrome,"['ACFS', 'acrocardiofacial syndrome', 'cleft palate-cardiac defect-genital anomalies-ectrodactyly syndrome', 'CCGE', 'CCGE syndrome', 'cleft palate, CARDIAC defect, genital anomalies, and ectrodactyly']",0070419,600460,2008,C1838121,,,,C563936,,,,
mondo:0010891,lethal hemolytic anemia-genital anomalies syndrome,"['hemolytic anemia, lethal congenital nonspherocytic, with genital and other abnormalities', 'hemolytic anaemia lethal congenital nonspherocytic with genital and other abnormalities', 'water-West syndrome', 'hemolytic anemia lethal congenital nonspherocytic with genital and other abnormalities']",,600461,1046,C1838120,,,,C563935,,,,
mondo:0010893,"malignant hyperthermia, susceptibility to, 4","['MHS4', 'malignant hyperthermia susceptibility 4', 'malignant hyperthermia, susceptibility to, 4', 'Mhs4', 'malignant hyperthermia susceptibility type 4', 'malignant hyperthermia, susceptibility to, type 4', 'malignant hyperpyrexia susceptibility type 4']",,600467,,,,,,C535697,,,,
mondo:0010894,maturity-onset diabetes of the young type 3,"['MODY hepatocyte nuclear factor-1-alpha related', 'maturity-onset diabetes of the young, type 3', 'MODY type 3', 'diabetes mellitus MODY type 3', 'type 3 maturity-onset diabetes of the young', 'HNF1A maturity-onset diabetes of the young (disease)', 'hepatocyte nuclear Factor 1-Alpha-associated monogenic diabetes', 'MODY3', 'MODY, type III', 'HNF1A-associated monogenic diabetes', 'MODY, type 3']",0111102,600496,,C1838100,,C129742,,C563933,,,,
mondo:0010895,ABCD syndrome,"['ABCDS', 'ABCD syndrome', 'albinism, black lock, cell migration disorder of the Neurocytes of the gut, and deafness', 'albinism, block lock, cell migration disorder of the neurocytes of the gut, and deafness']",0050600,600501,918,CN206498,"['-0.02057', '0.02812', '0.011536', '-0.01041', '0.003479', '-0.0495', '0.003447', '0.0632', '-0.02838', '-0.01941', '-0.00504', '-0.004837', '-0.000529', '0.02513', '-0.00575', '-0.0232', '0.001885', '-0.01997', '-0.02237', '-0.0755', '-0.002352', '-0.006355', '0.02892', '-0.0159', '0.006145', '-0.013016', '-0.000797', '-0.00884', '0.0221', '-0.01956', '0.03195', '-0.007812', '0.0411', '0.02101', '0.003271', '-0.01584', '-0.0094', '-0.01248', '-0.006557', '-0.0402', '0.01458', '-0.0366', '0.01819', '-0.01222', '0.01027', '-0.05585', '-0.02684', '0.03357', '-0.0002365', '0.005646', '-0.00969', '0.001875', '0.00402', '-0.00472', '-0.01729', '-0.02205', '0.03076', '-0.003847', '-0.05093', '0.0009375', '0.0245', '0.00956', '-0.002352', '-0.000518', '-0.003782', '0.00855', '0.0469', '0.012146', '-0.03696', '0.0616', '-0.0302', '-0.0006704', '0.01947', '-0.0208', '0.01402', '0.01752', '0.000879', '0.000429', '-0.02873', '-0.01163', '0.006927', '-0.00612', '-0.02345', '0.03952', '0.00847', '0.005493', '0.007492', '0.04886', '0.04752', '0.00397', '0.015594', '0.0363', '0.00448', '0.01956', '0.0656', '0.02168', '0.03008', '-0.0642', '-0.01195', '0.01447']",,,C535334,,,,
mondo:0010896,pigment dispersion syndrome,"['GPDS1', 'glaucoma-related pigment dispersion syndrome', 'glaucoma, pigment-dispersion type', 'pigment-dispersion type glaucoma', 'glaucoma-RELATED pigment dispersion syndrome', 'pigment dispersion syndrome', 'pigment-dispersion syndrome']",0060680,600510,26823,C1271398,,C187288,,C563184,,,,
mondo:0010897,schizophrenia 3,"['SCZD3', 'schizophrenia susceptibility locus, chromosome 6-related', 'schizophrenia 3 with or without an affective disorder', 'schizophrenia 3']",0070079,600511,,C1838069,,,,,,,,
mondo:0010898,autosomal dominant epilepsy with auditory features,"['autosomal dominant partial epilepsy with auditory features', 'epilepsy, familial temporal lobe, type 1', 'autosomal dominant lateral temporal lobe epilepsy', 'epilepsy, familial temporal lobe 1', 'familial temporal lobe epilepsy type 1', 'ADPEAF', 'epilepsy, partial, with auditory features', 'familial temporal lobe epilepsy 1', 'epilepsy, familial temporal lobe, 1', 'partial epilepsy with auditory features', 'ETL1', 'partial epilepsy with auditory aura', 'autosomal dominant epilepsy with auditory features', 'ADEAF', 'epilepsy, lateral temporal lobe, autosomal dominant', 'ADLTE']",0060748,,101046,C1838062,"['1.069', '0.375', '-0.4736', '-0.1372', '-0.6265', '-0.2664', '0.929', '0.518', '-0.5312', '-0.617', '-0.1965', '-0.255', '-0.3267', '0.3726', '-0.01367', '0.02484', '-0.6133', '-0.6763', '-0.1968', '-0.3616', '-0.22', '0.5396', '0.08594', '-0.1543', '-0.2277', '0.05853', '-0.396', '-0.1915', '-0.518', '0.1803', '0.4087', '-0.7163', '0.1547', '0.275', '0.5405', '0.1951', '0.02057', '0.1242', '-0.1843', '-0.488', '0.10034', '-0.3223', '0.1727', '-0.2542', '-0.2737', '-0.6475', '-0.2563', '0.2339', '0.1989', '0.927', '0.0619', '-0.002863', '-0.001591', '-0.4238', '0.3667', '-0.1812', '-0.2433', '-0.04538', '0.0433', '0.3088', '-0.7256', '0.5454', '0.401', '-0.313', '-0.3213', '1.239', '0.2306', '0.08026', '-0.637', '0.532', '0.7617', '0.869', '0.0441', '-0.414', '0.1305', '0.7393', '0.9307', '0.1504', '-0.2554', '0.129', '0.1631', '0.5273', '0.539', '0.2467', '0.2405', '0.2008', '0.1758', '0.728', '0.5737', '0.555', '0.1543', '0.224', '-0.3535', '0.1521', '0.06616', '0.03265', '0.493', '-0.155', '0.2998', '0.3987']",,,C537297,,,,
mondo:0010899,autosomal dominant nocturnal frontal lobe epilepsy 1,"['CHRNA4 autosomal dominant nocturnal frontal lobe epilepsy', 'nocturnal frontal lobe epilepsy 1', 'autosomal dominant nocturnal frontal lobe epilepsy type 1', 'autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNA4', 'ENFL1', 'epilepsy, nocturnal frontal lobe, type 1', 'epilepsy, nocturnal frontal lobe, 1']",0060682,600513,,C1838049,,,,C563930,,,,
mondo:0010900,intrauterine growth retardation with increased mitomycin c sensitivity,['intrauterine growth retardation with increased mitomycin c sensitivity'],,600546,,,,,,C536744,,,,
mondo:0010901,HEC syndrome,"['communicating hydrocephalus, endocardial fibroelastosis (EFE) and congenital cataracts', 'HEC syndrome', 'hydrocephalus, endocardial fibroelastosis, and cataracts', 'hydrocephalus-endocardial fibroelastosis-cataract syndrome']",,600559,2119,C1833607,,,,C535855,,,,
mondo:0010902,"spondyloepiphyseal dysplasia, Reardon type",['spondyloepiphyseal dysplasia with atlantoaxial instability'],,600561,163662,C1833603,,,,C563472,,,,
mondo:0010903,"craniosynostosis, Adelaide type","['craniosynostosis, Adelaide type', 'CRSA']",,600593,,C1833578,,,,C563471,,,,
mondo:0010904,"setting-Sun phenomenon, familial benign","['setting-Sun phenomenon, familial benign']",,600598,,C1833577,,,,C563470,,,,
mondo:0010905,cone-rod dystrophy 1,"['cone-rod retinal dystrophy-1', 'Crd1', 'cone-rod dystrophy type 1', 'cone-rod dystrophy 1', 'CRD1', 'CORD1']",0111009,600624,,C1833564,,,,C563469,,,,
mondo:0010906,orofacial cleft 11,"['orofacial cleft caused by mutation in BMP4', 'orofacial cleft type 11', 'cleft lip with or without cleft palate, nonsyndromic, 11', 'cleft Lip, congenital Healed', 'orofacial cleft 11', 'OFC11', 'BMP4 orofacial cleft', 'congenital Healed cleft lip']",0080404,600625,,C2677434,,,,,,,,
mondo:0010907,familial hypertryptophanemia,"['HYPTRP', 'hypertryptophanemia', 'hypertryptophanemia, familial']",0111703,600627,2224,C2931837,"['-0.4104', '0.4827', '0.1786', '0.228', '0.4082', '0.1501', '-0.1691', '0.475', '-0.0864', '-0.2683', '0.701', '-0.2235', '0.344', '0.3125', '-1.026', '0.102', '-0.4595', '0.3323', '-0.7036', '-0.4944', '-0.1831', '-0.3933', '0.0664', '-0.366', '0.8374', '-0.4197', '0.1492', '-0.5083', '0.4968', '0.2583', '-0.1268', '-0.02449', '0.848', '0.31', '0.2285', '-0.2083', '-0.9526', '-0.7183', '0.3684', '-0.2219', '-0.4712', '0.111', '-0.2502', '-0.2922', '-0.702', '-0.7056', '0.6167', '0.252', '0.227', '-0.1838', '0.1255', '0.77', '0.4138', '0.04483', '0.7383', '-0.5713', '0.09436', '0.1073', '-0.847', '0.09296', '0.1447', '0.1467', '-0.1464', '-0.2761', '-0.011215', '0.1992', '-0.18', '0.798', '-0.647', '0.7124', '0.791', '-0.1619', '-0.7974', '-0.5073', '0.1125', '0.948', '0.375', '0.339', '-0.1017', '0.3801', '0.2096', '-0.1759', '0.0669', '-0.00174', '0.684', '-0.4697', '-0.6826', '0.2091', '0.4739', '-0.0321', '0.748', '0.3872', '-0.0646', '-0.0698', '0.8096', '0.9517', '0.3682', '-0.1616', '0.6313', '-0.4143']",,,C538393,,,,
mondo:0010908,loose anagen syndrome,['loose anagen hair syndrome'],0111702,600628,168,C0406468,"['-0.2098', '0.2251', '-0.0934', '-0.1843', '0.4138', '-0.11633', '-0.05112', '0.2452', '-0.04672', '-0.08887', '-0.1117', '-0.02196', '-0.1936', '0.2253', '-0.21', '0.02002', '0.1779', '-0.2554', '0.0979', '-0.367', '-0.2091', '-0.1642', '0.02846', '-0.2522', '0.2532', '0.0464', '-0.202', '-0.1475', '0.1445', '0.194', '0.358', '-0.1489', '-0.2018', '0.445', '0.04846', '0.261', '-0.12445', '-0.07086', '-0.006077', '-0.4963', '0.2395', '-0.0865', '-0.1323', '-0.3325', '0.1775', '-0.4336', '-0.1718', '0.35', '0.3455', '-0.306', '-0.02028', '0.0161', '0.2664', '0.2532', '-0.1907', '0.01133', '0.1527', '-0.0998', '-0.2947', '-0.04684', '0.01843', '0.2009', '-0.00541', '0.1523', '0.36', '0.05606', '0.3057', '0.3035', '0.0478', '0.823', '-0.01349', '-0.1161', '0.2527', '0.10956', '-0.2656', '-0.2336', '-0.2396', '0.4553', '0.00889', '-0.8223', '0.0777', '-0.2566', '0.1289', '0.02724', '0.0752', '-0.203', '0.06006', '0.1296', '0.514', '0.5127', '0.12445', '0.4397', '-0.1434', '0.5947', '0.2744', '-0.485', '0.3716', '-0.54', '0.11115', '0.2522']",,,D058247,704.8,,,
mondo:0010909,UV-sensitive syndrome 1,"['UV-sensitive syndrome 1', 'ERCC6 UV-sensitive syndrome', 'UVSS1', 'UV-sensitive syndrome type 1', 'UV-sensitive syndrome caused by mutation in ERCC6']",,600630,,C3551173,,C173106,,,,,,
mondo:0010910,"enuresis, nocturnal, 1","['enuresis, nocturnal, 1', 'ENUR1', 'Bedwetting']",,600631,,,,,,,,,,
mondo:0010911,prolactin-producing pituitary gland adenoma,"['pituitary gland prolactinoma', 'lactotrope adenoma', 'prolactin producing pituitary adenoma', 'prolactin producing pituitary gland adenoma', 'prolactinoma', 'PRL producing pituitary gland adenoma', 'prolactin secreting adenoma of the pituitary gland', 'prolactinoma, familial', 'prolactin secreting adenoma of the pituitary', 'prolactin-producing pituitary gland adenoma', 'prolactinoma of the pituitary', 'prolactin secreting adenoma', 'prolactin secreting adenoma of pituitary', 'Forbes-Albright syndrome (formerly)', 'pituitary lactotrophic adenoma', 'prolactinoma of the pituitary gland', 'familial prolactinoma', 'prolactin-secreting pituitary adenoma', 'prolactin secreting pituitary adenoma', 'pituitary adenoma, prolactin-secreting', 'prolactin producing adenoma of pituitary gland', 'prolactinoma of pituitary', 'prolactin producing adenoma of the pituitary gland', 'lactotroph cell adenoma', 'prolactin secreting adenoma of pituitary gland', 'prolactinoma of pituitary gland', 'prolactin producing adenoma of pituitary', 'pituitary prolactinoma', 'PRLoma', 'prolactin producing adenoma of the pituitary', 'lactotroph adenoma', 'PRL-secreting pituitary adenoma', 'prolactin secreting pituitary gland adenoma']",5394,600634,2965,C0033375,"['-0.6465', '0.2444', '-0.3413', '-0.1399', '-0.26', '0.4653', '0.3533', '0.2703', '-0.01332', '-0.728', '-0.0956', '-0.1514', '0.1141', '0.9756', '-0.1333', '-0.5503', '-0.1063', '-0.2087', '-0.2063', '-0.515', '-0.573', '-0.6885', '0.2175', '-0.4978', '0.1566', '0.10333', '-0.3906', '-0.3965', '-0.3152', '-0.1003', '1.124', '-0.02882', '0.7007', '0.2588', '0.121', '-0.2263', '0.11664', '-0.304', '-0.4575', '0.6177', '0.0789', '0.2354', '0.69', '-0.5146', '0.2189', '-0.3367', '-0.3467', '-0.53', '-0.04318', '0.898', '0.3662', '0.533', '-0.4124', '-0.1235', '-0.1533', '0.8193', '0.5347', '-0.2247', '-0.361', '0.3118', '0.2966', '0.7935', '-0.4495', '-0.0959', '-0.371', '0.399', '-0.0733', '0.4907', '-0.3413', '0.34', '0.312', '-0.2378', '0.1835', '-0.3113', '0.0626', '-0.09125', '0.2783', '-0.1469', '-0.1838', '-0.725', '0.10443', '0.1422', '0.12', '0.5093', '-0.3298', '-3.904e-05', '0.38', '-0.889', '0.738', '-0.2744', '-0.0006533', '-0.348', '-0.2124', '-0.0351', '1.237', '-0.167', '0.5728', '-0.03833', '-0.651', '0.3474']",C3342,1000496,D015175,,E22.1,10036832,
mondo:0010912,"fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement","['congenital fibrosis of extraocular muscles caused by mutation in TUBB3', 'TUBB3 congenital fibrosis of extraocular muscles', 'fibrosis of extraocular muscles, congenital, 3A, with or without extraocular involvement', 'CFEOM3A', 'fibrosis of extraocular muscles, congenital, 3A', 'Feom3 locus']",0081017,600638,,C2748801,,,,C567572,,,,
mondo:0010913,Caroli disease,"['Caroli disease isolated', 'CAROLI disease, isolated', 'cystic dilatation of the intrahepatic biliary tree', 'congenital polycystic dilatation of intrahepatic bile ducts']",0050876,600643,53035,C1833541,,C84619,1001286,D016767,,,10013003,
mondo:0010914,"carnitine palmitoyl transferase II deficiency, severe infantile form","['Carnitine palmitoyl transferase deficiency type 2, hepatocardiomuscular form', 'CPT2, severe infantile form', 'CPT2, hepatocardiomuscular form', 'CPTII, hepatocardiomuscular form', 'CPTII, severe infantile form', 'Carnitine palmitoyl transferase deficiency type 2, severe infantile form', 'CARNITINE PALMITOYLTRANSFERASE II deficiency, infantile', 'Cpt2 deficiency, infantile', 'CPT 2 deficiency, hepatic', 'Carnitine Palmitoyltransferase 2 deficiency, infantile', 'CPT II deficiency, infantile', 'Carnitine Palmitoyltransferase 2 deficiency, hepatocardiomuscular', 'Carnitine Palmitoyltransferase 2 deficiency with hypoketotic hypoglycemia', 'Carnitine palmitoyl transferase II deficiency, hepatocardiomuscular form']",,600649,228305,C1833511,"['0.001984', '0.1844', '-0.3477', '0.4514', '-0.09076', '-0.5615', '0.0447', '0.3237', '-0.584', '0.05502', '-0.2087', '-0.0367', '0.2202', '0.2896', '-0.5317', '-0.333', '-0.1536', '-0.1941', '-0.3435', '-0.683', '0.4446', '-0.7124', '0.719', '-0.53', '-0.5645', '-0.2698', '-0.3188', '-0.2903', '0.137', '0.05045', '0.4446', '0.654', '0.293', '-0.3533', '-0.6206', '-0.655', '-0.3718', '-0.3071', '0.1775', '-0.0449', '-0.2017', '-1.175', '0.4817', '0.2081', '0.434', '0.11053', '0.177', '0.2126', '-0.2327', '0.551', '-0.01557', '-0.02525', '0.3547', '-0.1487', '0.174', '-0.452', '0.277', '0.1044', '0.02478', '0.6895', '0.551', '0.0555', '0.6885', '-0.202', '-0.1307', '0.2435', '0.426', '0.1891', '-0.808', '-0.1703', '-0.0755', '-0.2197', '0.2659', '0.259', '0.2412', '0.637', '-0.04318', '-0.1677', '-0.1749', '0.1864', '0.11615', '0.193', '-0.1517', '-0.1752', '0.527', '0.772', '0.1421', '0.03445', '0.884', '-0.2274', '0.154', '0.1743', '-0.03958', '0.2998', '-0.1175', '0.8877', '0.0811', '-0.4438', '-0.2216', '-0.4182']",,,C563462,,,,
mondo:0010915,autosomal dominant nonsyndromic hearing loss 4A,"['deafness, autosomal dominant 4A', 'autosomal dominant nonsyndromic deafness 4A', 'deafness, autosomal dominant 4a', 'autosomal dominant nonsyndromic deafness caused by mutation in MYH14', 'deafness, autosomal dominant 4', 'deafness, autosomal dominant type 4A', 'DFNA4A', 'autosomal dominant deafness 4A', 'autosomal dominant nonsyndromic deafness type 4A', 'MYH14 autosomal dominant nonsyndromic deafness']",0110573,600652,,C1833503,,,,C563460,,,,
mondo:0010916,polycystic kidney disease 3 with or without polycystic liver disease,"['GANAB autosomal dominant polycystic kidney disease', 'polycystic kidney disease 3, autosomal dominant', 'Apkd3', 'Pkd3', 'polycystic kidney disease type 3', 'PKD3', 'polycystic kidney disease 3', 'polycystic kidney disease, adult, type 3', 'polycystic kidney disease, adult, type III', 'polycystic kidney disease, type 3', 'polycystic kidney disease 3 with or without polycystic liver disease', 'autosomal dominant polycystic kidney disease caused by mutation in GANAB']",0110860,600666,,C3887964,,,,,,,,
mondo:0010917,chondrocalcinosis 1,"['CCAL1', 'chondrocalcinosis with early-onset osteoarthritis', 'chondrocalcinosis 1']",,600668,,,,,,C535938,,,,
mondo:0010918,"epilepsy, idiopathic generalized, susceptibility to, 1","['EIG', 'epilepsy, idiopathic generalized, susceptibility to, 1', 'EIG1']",,,,,,,,C562694,345.10,,,
mondo:0010919,"varicella, severe recurrent","['varicella, severe recurrent']",,600670,,C1833487,,,,C563458,,,,
mondo:0010920,microtia,"['microtia-anotia', 'congenital microtias', 'microtias, congenital', 'M-A', 'microtia, congenital', 'anotia']",,600674,93976,,,,,D065817,744.23,Q17.2,10027555,
mondo:0010921,nasal dermoid cyst,"['dermoid cysts, familial frontonasal', 'nasal dermoid sinus cyst']",,600679,141103,C1833473,,,,C563455,,,,
mondo:0010922,Satoyoshi syndrome,"['muscle spasms, intermittent with alopecia, diarrhea and skeletal abnormalities', 'muscle spasms, intermittent with alopecia, diarrhoea and skeletal abnormalities', 'Satoyoshi syndrome', 'muscle spasms, intermittent, with alopecia, diarrhea, and skeletal abnormalities', 'Komuragaeri disease']",,600705,3130,C1833454,,,,C536616,,,10070579,
mondo:0010923,proximal myopathy with focal depletion of mitochondria,['proximal myopathy with focal depletion of mitochondria'],,600706,521305,C1833453,,,,C563453,,,,
mondo:0010924,D-2-hydroxyglutaric aciduria,"['D-2-hydroxyglutaric acidemia', 'D2HA', 'D-2-hydroxyglutaric aciduria 1', 'D2HGA', 'D-2-HGA', 'D-2-hydroxyglutaric aciduria type 1']",0050575,,79315,CN233040,"['-0.424', '0.696', '-0.4683', '-0.3035', '0.1614', '-0.1155', '-0.1974', '0.948', '-0.7964', '7.91e-05', '-0.569', '-0.6665', '-0.253', '-0.4329', '-0.3376', '0.668', '0.252', '-0.09247', '-0.469', '-0.727', '0.0573', '-0.1831', '0.697', '0.04645', '0.1948', '-0.01162', '-0.3484', '0.03223', '-0.00843', '0.382', '0.101', '0.149', '0.4744', '-0.06137', '-0.0626', '-0.0726', '-0.6113', '-0.08435', '-0.2233', '0.2695', '0.2546', '-0.6533', '0.2822', '-0.975', '0.4773', '-0.00554', '0.3977', '0.3662', '0.0909', '0.3083', '-0.1019', '-0.06537', '-0.03488', '-0.1783', '-0.1487', '-0.00344', '0.1727', '-0.607', '-0.4087', '0.8936', '-0.10516', '-0.312', '0.581', '-0.5835', '-0.3057', '-0.3838', '0.2163', '0.2612', '-0.8613', '0.571', '0.1771', '0.1361', '-0.384', '0.572', '0.011765', '0.921', '0.8306', '0.1486', '0.2546', '0.2351', '0.7275', '-0.4236', '-0.7476', '0.2947', '-0.02144', '0.2695', '0.04602', '0.2986', '0.0603', '0.69', '-0.0398', '0.1558', '-0.539', '-0.0606', '0.651', '0.5957', '0.1526', '-0.0753', '-0.0495', '-0.0386']",,,,,,,
mondo:0010925,velo-facial-skeletal syndrome,['VELOFACIOSKELETAL syndrome'],,600736,3424,C1833380,,,,C536536,,,,
mondo:0010926,familial hypocalciuric hypercalcemia 3,"['FBH3', 'FBHOk', 'FHH type 3', 'hypocalciuric hypercalcemia type III', 'familial benign hypercalcemia, Oklahoma variant', 'AP2S1 familial hypocalciuric hypercalcemia', 'familial hypocalciuric hypercalcemia type 3', 'hypercalcemia, familial benign, Oklahoma type', 'hypocalciuric hypercalcemia, familial, type 3', 'familial hypocalciuric hypercalcemia caused by mutation in AP2S1', 'hypercalcemia, familial benign, type 3', 'familial benign hypercalcemia, type 3', 'HHC3', 'hpocalciuric hypercalcemia, type III', 'hypocalciuric hypercalcemia, familial, type III']",0060702,600740,101050,C1833372,"['0.1769', '0.1272', '0.7886', '-0.06635', '-0.08057', '0.2279', '-0.2372', '0.4663', '-0.737', '-0.2349', '0.00585', '0.2295', '-0.923', '0.6914', '-0.1718', '-0.575', '-0.632', '0.1604', '-0.1903', '-0.319', '0.5117', '-0.5083', '-0.1418', '-0.6743', '0.8267', '-0.713', '0.619', '-0.747', '0.0737', '-0.3726', '0.00896', '0.00899', '0.42', '-0.1592', '-0.9224', '-0.653', '-0.3691', '0.1692', '0.3862', '-0.416', '0.0696', '-0.38', '0.411', '-0.6475', '0.665', '-0.3005', '0.02664', '0.0884', '0.2323', '0.7017', '-0.1826', '0.6562', '0.5376', '-0.2234', '-0.9443', '0.0502', '-0.5957', '0.6543', '0.1179', '0.3647', '0.3433', '0.1532', '-0.0661', '-0.6245', '-0.556', '0.2086', '0.1186', '0.5', '-0.588', '0.07874', '0.1687', '0.5493', '0.2844', '-0.3586', '-0.0823', '1.2295', '-0.3105', '1.416', '0.6167', '0.3254', '-0.655', '-0.463', '0.01363', '0.11096', '0.407', '0.02104', '0.3445', '0.02852', '0.8135', '0.611', '-0.02463', '0.2175', '-0.514', '-0.2018', '0.8403', '0.908', '0.1538', '-0.354', '-0.594', '0.1131']",,,C537147,,,,
mondo:0010927,orofacial cleft 3,"['OFC3', 'orofacial cleft 3', 'cleft lip with or without cleft palate, nonsyndromic, 3']",0080397,600757,,C1833369,,,,C563448,,,,
mondo:0010928,"dwarfism, familial, with muscle spasms","['familial dwarfism and painful muscle spasms', 'dwarfism, familial, with muscle spasms', 'dwarfism familial with muscle spasms']",,600771,,C1833341,,,,C563447,,,,
mondo:0010929,craniosynostosis 4,"['ERF craniosynostosis', 'CRS4', 'craniosynostosis caused by mutation in ERF', 'craniosynostosis type 4', 'craniosynostosis 4', 'ERF-related craniosynostosis']",,600775,35093,C3806917,"['-0.2053', '-0.05396', '-0.1113', '-0.1888', '0.05582', '-0.01654', '0.3086', '0.3352', '-0.8354', '0.05322', '-0.1633', '0.0007925', '0.0482', '0.06635', '-0.1549', '-0.1755', '0.221', '-0.2224', '0.3694', '-0.4006', '-0.003721', '0.317', '0.2615', '-0.2177', '0.1385', '0.2222', '-0.03326', '-0.02794', '0.382', '0.2144', '0.1741', '-0.404', '0.191', '-0.07465', '0.208', '-0.03067', '0.2367', '-0.2783', '-0.2418', '-0.733', '0.1946', '0.0389', '0.1453', '-0.61', '0.2861', '0.09094', '-0.3225', '0.355', '-0.1093', '0.3796', '0.04358', '-0.1685', '0.2458', '0.1261', '-0.4504', '-0.292', '0.1293', '0.083', '0.1267', '0.2372', '0.173', '-0.2761', '-0.04712', '-0.0861', '-0.3125', '-0.09015', '0.3962', '0.5293', '-0.01266', '0.5176', '-0.233', '0.3494', '0.3394', '-0.1624', '-0.2637', '0.3171', '0.1608', '0.06604', '-0.4167', '-0.4731', '-0.2544', '0.227', '-0.0415', '0.4373', '0.1937', '-0.2252', '-0.0794', '0.1268', '0.0275', '-0.1554', '-0.5522', '0.344', '0.168', '0.1377', '0.751', '-0.2129', '0.5815', '-0.5156', '0.2162', '-0.01513']",,,,,,,
mondo:0010930,anophthalmia plus syndrome,"['Fryns anophthalmia syndrome', 'Fryns microphthalmia syndrome', 'anophthalmia-plus syndrome', 'Leichtman Wood Rohn syndrome', 'microphthalmia with facial clefting', 'anophthalmia, cleft lip/palate, facial anomalies, and CNS anomalies and hypothalamic disorder']",,600776,1104,C1833339,,,,C537767,,,,
mondo:0010931,"vitamin D-dependent rickets, type 2B","['VDDR2B', 'hereditary 1,25 dihydroxyvitamin D-resistant rickets with abnormal vitamin D receptor without alopecia', 'vitamin D-dependent rickets, type 2B, with normal vitamin D receptor', 'vitamin D dependent rickets 2b', 'vitamin D-dependent rickets type II without alopecia', 'vitamin D resistant rickets', 'vitamin D receptor signalling defect rickets', 'vitamin D receptor signaling defect rickets']",0080885,600785,,C2748783,,C131076,,,,,,
mondo:0010932,progressive bifocal chorioretinal atrophy,"['chorioretinal atrophy, progressive bifocal', 'PBCRA', 'CRAPB', 'progressive bifocal chorioretinal atrophy', 'Crapb']",,600790,75373,C1833321,,,,C535356,,,,
mondo:0010933,autosomal recessive nonsyndromic hearing loss 4,"['deafness, autosomal recessive 4, with enlarged vestibular aqueduct', 'autosomal recessive deafness 4 with enlarged vestibular aqueduct', 'DFNB4', 'neurosensory nonsyndromic recessive deafness 4', 'autosomal recessive nonsyndromic deafness 4', 'enlarged vestibular aqueduct, digenic', 'enlarged vestibular aqueduct', 'autosomal recessive nonsyndromic deafness type 4', 'dilated vestibular aqueduct']",0110498,600791,,,,,,C566366,,,,
mondo:0010936,frontotemporal dementia and/or amyotrophic lateral sclerosis 7,"['dementia, familial nonspecific', 'CHMP2B-related amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis caused by mutation in CHMP2B', 'CHMP2B amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis, Chmp2B-related', 'Dmt1', 'FTD3', 'frontotemporal dementia, chromosome 3-linked']",0111227,614696,,C1836076,,,,C579991,331.19,,,
mondo:0010937,isoproterenol-mediated vasodilatation,['isoproterenol-mediated vasodilatation'],,600801,,C1833276,,,,,,,,
mondo:0010938,T-B+ severe combined immunodeficiency due to JAK3 deficiency,"['SCID, T cell-negative, B cell-positive, NK cell-negative', 'SCID, autosomal recessive, T-negative/B-positive type', 'T-B+ SCID due to JAK3 deficiency', 'severe combined immunodeficiency, autosomal recessive, T cell-NEGATIVE, B cell-POSITIVE, NK cell-NEGATIVE']",,600802,35078,C4273742,"['-0.5757', '0.678', '0.11115', '-0.1177', '0.3196', '-0.4963', '0.2336', '0.265', '0.0391', '-0.3933', '-0.2487', '-0.02962', '-0.626', '-0.2086', '-0.09784', '-0.166', '0.1036', '-0.0417', '-0.3213', '-0.778', '-0.1036', '-0.6567', '1.056', '-0.1753', '0.382', '0.368', '-0.1896', '0.2244', '-0.0766', '-0.561', '0.3494', '0.716', '0.3088', '-0.1272', '-0.013985', '-0.2532', '-0.5947', '0.10675', '-0.453', '0.02338', '-0.3555', '-0.3945', '0.1863', '-0.0916', '-0.646', '-0.1287', '-0.2395', '-0.8335', '0.217', '0.1501', '0.2074', '-0.3193', '0.11584', '-0.3025', '-0.3381', '0.1092', '0.1997', '-0.4202', '-0.0827', '0.2306', '0.1122', '0.522', '-0.04504', '0.00397', '0.848', '-0.2408', '0.5273', '0.1998', '-0.3787', '0.344', '-0.061', '0.0992', '0.1716', '-0.2006', '0.403', '-0.06635', '0.4841', '-0.1611', '0.0604', '0.0861', '0.1227', '-0.393', '-0.0994', '-0.253', '-0.3093', '-0.2322', '0.4824', '0.7495', '0.3442', '-0.0618', '0.2993', '0.1512', '-0.4395', '-0.1343', '0.5913', '1.432', '0.001575', '-0.7607', '-0.0697', '0.03412']",,,C563440,,,,
mondo:0010939,low phospholipid associated cholelithiasis,"['ABCB4 gene mutation-associated cholelithiasis', 'LPAC', 'cholelithiasis, Low phospholipid-associated', 'gallbladder disease 1', 'GBD1', 'cholelithiasis with ABCB4 gene mutation', 'gallbladder disease type 1']",,600803,69663,C2609268,"['-0.04147', '-0.05582', '0.132', '-0.0844', '0.0408', '-0.01584', '0.1257', '0.2095', '-0.1686', '-0.09045', '-0.1018', '0.0873', '-0.048', '0.1172', '-0.2212', '-0.4587', '0.0649', '0.1714', '-0.02582', '-0.445', '0.0502', '-0.3296', '0.2452', '-0.1392', '0.06354', '-0.1582', '0.206', '0.2081', '-0.03047', '-0.379', '0.3674', '-0.01424', '0.2554', '0.1603', '0.04102', '-0.2167', '-0.2979', '-0.01132', '0.0001792', '-0.05017', '-0.1448', '-0.04532', '0.5195', '-0.1069', '-0.393', '-0.11096', '0.2644', '0.01284', '-0.01107', '0.11206', '-0.1411', '0.2169', '0.1825', '-0.2444', '0.00411', '-0.01866', '0.1169', '-0.2134', '-0.4282', '0.10693', '0.3586', '0.3628', '0.1494', '-0.3716', '0.2664', '-0.1451', '0.2988', '0.4565', '-0.1365', '0.1648', '0.11', '-0.003105', '0.1874', '-0.0742', '0.2712', '-0.1539', '0.3264', '0.1173', '-0.0933', '0.06158', '-0.3447', '-0.1043', '-0.0538', '0.06192', '-0.058', '-0.02798', '0.1788', '-0.07556', '0.3445', '-0.1481', '0.1974', '0.3555', '-0.03546', '-0.2363', '0.4478', '0.3157', '0.3416', '-0.1812', '-0.4402', '0.03372']",,,,,,10068936,
mondo:0010940,inherited susceptibility to asthma,"['asthma-related traits, susceptibility to', 'asthma, bronchial', 'asthma, nocturnal, susceptibility to', 'asthma, diminished response to Antileukotriene treatment 1N', 'asthma, protection against', 'asthma, susceptibility to']",,600807,,,"['-0.01218', '0.05627', '0.00438', '-0.02385', '0.02356', '-0.0904', '0.02928', '0.03632', '-0.0354', '-0.051', '0.02133', '0.00717', '-0.003149', '0.02135', '-0.03232', '-0.04095', '-0.009125', '-0.02301', '-0.05173', '-0.12146', '0.004356', '-0.0435', '0.0741', '-0.01382', '-0.01814', '-0.02542', '-0.004044', '0.01091', '0.005943', '-0.04453', '0.08', '-0.01154', '0.06247', '0.00303', '0.02432', '-0.01799', '-0.02753', '-0.03806', '-0.00769', '-0.0783', '0.02774', '-0.05362', '0.04047', '-0.02658', '-0.001016', '-0.0837', '0.005184', '0.03784', '0.02913', '0.03836', '-0.02597', '-0.0128', '0.02963', '0.00692', '0.00845', '-0.0009665', '0.05566', '-0.01965', '-0.0673', '-0.0008807', '0.04492', '0.05945', '0.00562', '0.015564', '0.02783', '0.03644', '0.084', '0.08325', '-0.0807', '0.1267', '-0.0739', '-0.02606', '-0.01208', '-0.04507', '0.02954', '0.03748', '0.01001', '-0.01322', '-0.01918', '-0.03687', '-0.012985', '0.00408', '-0.01183', '0.0943', '-0.02979', '0.007107', '0.04022', '0.03598', '0.0722', '0.02437', '0.05182', '0.04398', '-0.01968', '0.02744', '0.1222', '0.0764', '0.0671', '-0.0728', '-0.0477', '0.01317']",,,,,,,
mondo:0010941,"nocturnal enuresis, 2","['enuresis, nocturnal, 2', 'ENUR2']",,600808,,C1833268,,,,C563439,,,,
mondo:0010943,schizophrenia 4,"['schizophrenia, susceptibility to, 4', 'schizophrenia 4', 'schizophrenia type 4', 'schizophrenia susceptibility locus, chromosome 22Q11-related', 'SCZD4']",0070080,600850,,C1833247,,,,,,,,
mondo:0010944,mitochondrial import-stimulating factor,"['MSF', 'mitochondrial import-stimulating factor']",,600851,,,,,,,,,,
mondo:0010945,retinitis pigmentosa 17,"['retinitis pigmentosa caused by mutation in CA4', 'RP 17', 'retinitis pigmentosa type 17', 'CA4 retinitis pigmentosa', 'RP17', 'retinitis pigmentosa 17']",0110404,600852,,C1833245,,,,C563437,,H35.5,,
mondo:0010946,hypertrophic cardiomyopathy 6,"['cardiomyopathy, familial hypertrophic, type 6', 'cardiomyopathy, familial hypertrophic 6', 'cardiomyopathy, familial hypertrophic, 6', 'CMH6', 'cardiomyopathy, hypertrophic 6', 'PRKAG2 hypertrophic cardiomyopathy', 'hypertrophic cardiomyopathy type 6', 'hypertrophic cardiomyopathy caused by mutation in PRKAG2']",0110312,600858,,C1833236,"['-0.010025', '0.07367', '0.01438', '0.010666', '0.02852', '-0.0745', '0.02376', '0.0973', '-0.05484', '0.004932', '-0.0305', '0.006477', '-0.005215', '-0.02965', '-0.03412', '-0.05353', '-0.0302', '-0.01888', '-0.011185', '-0.0971', '-0.002234', '-0.02977', '0.0404', '0.007374', '0.02634', '-0.01833', '0.001365', '0.01721', '-0.003407', '-0.02507', '0.04404', '-0.01604', '0.07623', '0.02689', '-0.01514', '-0.04742', '-0.0224', '-0.02888', '-0.003105', '-0.03506', '-0.004562', '-0.0502', '0.0455', '0.02658', '-0.0057', '-0.01979', '-0.01347', '0.0478', '-0.00785', '0.01785', '-0.057', '-0.02103', '0.007626', '0.015076', '0.003216', '-0.03262', '0.04208', '-0.001753', '-0.06506', '0.00974', '0.0239', '0.03072', '0.02348', '0.01633', '-0.02423', '-0.003632', '0.09467', '0.06744', '-0.06793', '0.05634', '-0.0601', '0.002377', '0.01848', '-0.03102', '0.03772', '0.0282', '0.004807', '-0.03864', '-0.03702', '-0.013275', '0.012375', '-0.0003188', '-0.012184', '0.00969', '0.01923', '0.02113', '0.01787', '0.05756', '0.0822', '0.015526', '0.02089', '0.011696', '0.0001023', '0.02133', '0.1267', '0.04367', '0.03046', '-0.0633', '-0.01868', '-0.007004']",,,C563436,,,,
mondo:0010947,Budd-Chiari syndrome,"['BDCHS', 'Budd-Chiari syndrome', 'membranous obstruction of Inferior vena cava', 'membranous obstruction of the inferior vena cava', 'Budd-Chiari syndrome, somatic']",,600880,131,C0856761,,,,D006502,453.0,I82.0,10006537,
mondo:0010948,cataract 10 multiple types,"['CCZS', 'congenital zonular cataract with sutural opacities', 'cataract, congenital zonular, with sutural opacities', 'early-onset non-syndromic cataract caused by mutation in CRYBA1', 'CRYBA1 early-onset non-syndromic cataract', 'cataract 10, multiple types', 'CTRCT10']",0110258,600881,98995,C1833229,,,,C563435,,,,
mondo:0010949,Charcot-Marie-Tooth disease type 2B,"['Charcot-Marie-Tooth disease, axonal, type 2B', 'CMT 2B', 'Charcot Marie Tooth disease type 2B', 'HMSN2B', 'peripheral sensory neuropathy, autosomal dominant (PSN)', 'hereditary motor and sensory neuropathy 2B', 'HMSN IIB', 'RAB7A Charcot-Marie-Tooth disease type 2', 'CMT2B', 'hereditary motor and sensory nueropathy IIB', 'Charcot-Marie-Tooth disease, autosomal dominant, type 2B', 'Charcot-Marie-Tooth disease, neuronal, type 2B', 'Charcot-Marie-Tooth disease type 2 caused by mutation in RAB7A', 'Charcot-Marie-Tooth neuropathy, type 2B', 'Charcot-Marie-Tooth neuropathy type 2B', 'Charcot-Marie-Tooth disease, type 2B', 'hereditary motor and sensory neuropathy 2 B (HMSN 2 B)', 'autosomal dominant Charcot-Marie-Tooth disease type 2B']",0110159,600882,99936,C1833219,"['0.3213', '0.3884', '0.2395', '-0.01378', '-0.1531', '-0.4294', '-0.2084', '0.659', '-0.737', '-0.1526', '0.03992', '0.4512', '-0.4822', '0.1896', '-0.203', '-0.2053', '-0.3518', '-0.6606', '-0.393', '-0.728', '-0.2659', '0.1501', '0.2727', '0.6084', '0.3508', '0.6777', '-0.02998', '0.4753', '0.005062', '-0.08795', '0.04333', '-0.69', '0.2397', '0.5645', '0.4653', '-0.599', '-0.4868', '0.00975', '0.4038', '-0.352', '-1.578', '-0.3635', '-0.03418', '0.7705', '-0.1089', '-0.3628', '-0.005024', '0.1403', '-0.2676', '-0.1218', '0.1431', '0.4768', '0.2418', '-0.801', '0.3633', '-0.4558', '0.1298', '0.3496', '-0.5093', '0.1578', '-0.4502', '0.02574', '0.9062', '1.272', '-1.083', '1.195', '0.257', '0.3682', '-0.4783', '0.5996', '-0.726', '0.05243', '0.3386', '-0.1991', '1.374', '0.3525', '-0.478', '0.427', '0.1616', '-0.404', '-0.5', '-0.03232', '0.6577', '0.7266', '0.0812', '-0.0833', '0.0732', '0.4834', '0.5664', '0.1244', '0.3345', '-0.2072', '0.3901', '0.3845', '0.2856', '0.67', '0.7896', '-0.6587', '-0.2964', '0.4592']",,,C537989,,,,
mondo:0010950,type 1 diabetes mellitus 8,"['diabetes mellitus, insulin-dependent, 8', 'insulin-dependent diabetes mellitus 8', 'IDDM8']",0110747,600883,,C1833218,,,,C563433,,,,
mondo:0010951,dilated cardiomyopathy 1B,"['cardiomyopathy, familial dilated, 1', 'dilated cardiomyopathy type 1B', 'cardiomyopathy, dilated 1B', 'cardiomyopathy, familial dilated', 'cardiomyopathy, dilated, 1B']",0110443,600884,,,,,,,,,,
mondo:0010952,hereditary hyperferritinemia with congenital cataracts,"['hyperferritinemia, hereditary, with congenital cataracts', 'HHCS', 'Bonneau-Beaumont syndrome', 'hereditary hyperferritinemia cataract syndrome', 'HRFTC', 'cataract-hyperferritinemia syndrome', 'hyperferritinemia cataract syndrome', 'hyperferritinemia with or without cataract', 'hereditary hyperferritinemia-cataract syndrome', 'hyperferritinemia-cataract syndrome']",0111256,600886,163,C1833213,"['-0.0798', '-0.4443', '0.4578', '0.7476', '0.1103', '0.656', '-0.4714', '1.015', '-0.03113', '-0.4795', '-0.1565', '-0.548', '-0.1647', '1.091', '-0.2905', '0.306', '0.3752', '0.4863', '-0.0657', '-0.6973', '-0.03873', '0.1277', '0.0863', '0.04517', '0.1726', '-0.10614', '-0.0818', '0.2522', '0.385', '0.08124', '0.2683', '-0.3662', '0.532', '0.5786', '0.4238', '0.2803', '0.2229', '-0.7393', '0.311', '-0.967', '0.673', '-0.683', '-0.1338', '0.05164', '0.393', '0.11304', '0.4258', '0.07434', '0.5996', '-0.593', '0.4817', '0.0265', '0.7373', '-0.4985', '0.2495', '-0.1693', '0.637', '0.3923', '-0.7314', '-0.677', '-0.1726', '-0.2108', '0.5215', '-0.669', '0.05267', '0.596', '1.051', '0.5083', '0.543', '0.5273', '-0.1484', '0.704', '0.564', '-0.3044', '1.149', '0.1836', '0.2393', '0.11273', '-0.3315', '0.52', '-0.14', '0.05515', '-0.832', '0.1825', '-0.2688', '0.0932', '0.422', '0.1194', '1.128', '0.1469', '0.11633', '0.2416', '-0.2585', '0.3293', '-0.106', '-0.664', '-0.2595', '-0.3562', '-0.321', '-0.3704']",,,C538137,366.44,,,
mondo:0010953,Fanconi anemia complementation group E,"['FANCE Fanconi anemia', 'Fanconi anemia caused by mutation in FANCE', 'Fanconi anemia complementation group type E', 'Fanconi anemia, complementation group E', 'FANCE', 'Fanconi anaemia caused by mutation in FANCE', 'FANCE Fanconi anaemia', 'Fanconi anaemia complementation group type E', 'Fanconi Anemia, complementation group type E', 'face']",0111084,600901,,C3160739,"['-0.05994', '0.0944', '0.007603', '0.0187', '0.1265', '-0.125', '-0.049', '0.0618', '-0.01561', '-0.06714', '-0.01927', '0.007656', '-0.00893', '0.01868', '-0.001213', '-0.0982', '-0.0464', '-0.05307', '-0.001589', '-0.1737', '0.03607', '-0.06464', '0.1052', '0.005585', '0.0853', '-0.0802', '-0.003242', '-0.0336', '0.003925', '-0.075', '0.04547', '-0.01689', '0.10846', '0.087', '0.04602', '-0.0487', '-0.07336', '-0.143', '-0.0859', '-0.103', '-0.02269', '-0.1387', '0.05402', '-0.04636', '-0.0276', '-0.1785', '0.003101', '0.1095', '0.0793', '0.01694', '0.01852', '-0.01921', '0.01164', '0.02783', '-0.04962', '-0.1047', '0.04694', '0.00439', '-0.1969', '0.05328', '0.0656', '0.00962', '-0.01881', '-0.014755', '0.05063', '0.004364', '0.1067', '0.10925', '-0.07605', '0.1288', '-0.0758', '-0.0908', '0.002762', '-0.0818', '0.0398', '0.05768', '0.03168', '-0.05176', '-0.0271', '-0.03604', '-0.0087', '-0.05444', '-0.03717', '0.05283', '0.011795', '-0.04153', '0.04877', '0.1058', '0.187', '-0.00606', '0.1565', '0.05664', '0.01784', '-0.05768', '0.135', '0.1837', '0.0604', '-0.11053', '-0.00537', '0.10333']",C125709,,,,,,
mondo:0010954,"Wiskott-Aldrich syndrome, autosomal dominant form","['Wiskott-Aldrich syndrome, autosomal dominant form']",,600903,,C1833170,,,,C563431,,,,
mondo:0010955,ectodermal dysplasia with intellectual disability and syndactyly,"['ectodermal dysplasia mental retardation syndactyly', 'ectodermal dysplasia intellectual disability syndactyly', 'ectodermal dysplasia with intellectual disability and syndactyly', 'ectodermal dysplasia with mental retardation and syndactyly']",,600906,,C1833169,,,,C538018,,,,
mondo:0010956,"enamel hypoplasia, cataracts, and aqueductal stenosis","['Seow Najjar syndrome', 'enamel hypoplasia, capsular cataracts, and ductal stenosis', 'enamel hypoplasia, cataracts, and aqueductal stenosis']",,600907,,C1833163,,,,C563430,,,,
mondo:0010958,"cardiac arrhythmia, ankyrin-B-related","['cardiac arrhythmia, ankyrin-b-related', 'LQT4', 'ankyrin-B syndrome']",0111701,600919,101016,C1970119,,,,,,,,
mondo:0010959,van den Ende-Gupta syndrome,"['Marden-Walker-like syndrome', 'van den Ende-Gupta syndrome', 'Marden Walker like syndrome without psychomotor retardation', 'VAN DEN Ende-Gupta syndrome', 'Van den Ende Gupta syndrome', 'VDEGS', 'Marden Walker like syndrome', 'Marden-Walker-like syndrome without psychomotor retardation', 'blepharophimosis, arachnodactyly, and congenital contractures']",0111699,600920,2460,C1833136,"['-0.2642', '0.0548', '-0.003426', '-0.578', '0.1752', '-0.586', '-0.31', '0.517', '-0.571', '-0.3547', '0.002565', '0.01257', '0.04126', '0.0378', '0.3376', '0.3374', '0.1982', '-0.04114', '-0.01736', '-0.551', '-0.2732', '0.1077', '-0.05875', '-0.558', '0.2742', '0.1973', '-0.489', '-0.2057', '1.026', '-0.4275', '0.5557', '-0.3806', '0.003508', '0.2157', '0.08026', '-0.399', '0.01616', '-0.3757', '0.1633', '-0.5327', '-0.08093', '-0.3286', '-0.1619', '-0.1137', '-0.473', '-0.2576', '0.2194', '0.5093', '-0.4521', '-0.3894', '-0.683', '-0.1231', '-0.4082', '0.668', '-0.4475', '-0.3884', '0.1279', '-0.06088', '0.1343', '0.215', '0.3452', '0.1444', '-0.3447', '0.416', '-0.3179', '-0.2313', '-0.08185', '0.315', '-0.4978', '0.2537', '-0.5137', '0.533', '0.00932', '-0.05023', '-0.02473', '0.6445', '-0.001303', '-0.531', '-0.1996', '0.1321', '0.395', '0.2659', '0.2073', '0.8467', '0.2742', '0.4866', '-0.242', '0.712', '-0.099', '0.3733', '-0.02536', '0.5645', '0.2384', '0.447', '1.111', '0.1418', '0.4902', '-0.3147', '0.158', '0.103']",,,C535909,,,,
mondo:0010960,protocadherin 3,"['protocadherin type 3', 'protocadherin 3', 'Pcdh3']",,600931,,,,,,,,,,
mondo:0010961,obesity due to prohormone convertase I deficiency,"['obesity and endocrinopathy due to impaired processing of prohormones', 'proprotein convertase 1/3 deficiency', 'obesity with impaired prohormone processing', 'PCI deficiency']",0111698,600955,71528,C4302878,"['-0.2788', '0.2673', '-0.1636', '0.8677', '-0.09186', '-0.8203', '0.1162', '0.688', '-0.2451', '-0.5884', '-0.04108', '0.2642', '0.2428', '0.3337', '-0.765', '-0.569', '-0.3132', '0.847', '-0.876', '-0.7275', '0.01982', '-0.326', '0.2391', '-0.221', '0.263', '0.3472', '-0.4268', '-0.6323', '0.1361', '-0.3572', '0.3691', '-0.406', '0.485', '0.04922', '-0.2612', '-0.4365', '-0.633', '0.276', '0.56', '-0.04742', '-0.1095', '-0.3645', '-0.9644', '0.4397', '0.1512', '-0.716', '0.579', '-0.07544', '0.537', '0.1571', '-0.4705', '0.01174', '0.4758', '-0.3113', '-0.3447', '0.6724', '-0.2966', '-0.0984', '-0.2107', '-0.4836', '0.546', '0.3875', '-0.1536', '-0.653', '-0.011284', '0.7173', '-0.3425', '0.4258', '0.316', '0.4607', '0.2947', '0.4402', '-0.01226', '-0.186', '0.4814', '-0.57', '-0.1154', '0.0009494', '-1.154', '0.5415', '0.01262', '1.005', '0.0555', '0.02365', '0.9385', '0.7583', '0.3862', '0.2605', '0.905', '0.3713', '-0.1772', '0.5166', '-0.1578', '0.5806', '0.6665', '0.103', '0.07404', '-0.3867', '-0.4165', '-0.01135']",,,C563423,,,,
mondo:0010962,diffuse nonepidermolytic palmoplantar keratoderma,"['non-epidermolytic palmoplantar keratoderma', 'Unna-Thost palmoplantar keratoderma', 'diffuse NEPPK', 'autosomal dominant diffuse palmoplantar keratoderma, Norrbotten type', 'nonepidermolytic palmoplantar keratoderma', 'Thost-Unna palmoplantar keratoderma', 'diffuse nonepidermolytic palmoplantar keratoderma', 'keratoderma, nonepidermolytic palmoplantar', 'NEPPK', 'palmoplantar keratoderma, nonepidermolytic', 'Thost-Unna disease', 'Unna-Thost syndrome', 'tylosis', 'PPK diffusa circumscripta', 'KRT1-related diffuse nonepidermolytic keratoderma', 'Thost-Unna syndrome', 'PPKNE', 'diffuse palmoplantar keratoderma, Bothnian type']",0050428,600962,530838,,,,1000743,,,,,
mondo:0010963,autosomal dominant nonsyndromic hearing loss 6,"['DFNA14', 'deafness, autosomal dominant 38', 'autosomal dominant deafness 14', 'autosomal dominant nonsyndromic deafness caused by mutation in WFS1', 'autosomal dominant nonsyndromic deafness 6', 'deafness, autosomal dominant 6', 'deafness, autosomal dominant type 6', 'DFNA38', 'deafness, autosomal dominant 14', 'autosomal dominant deafness 6', 'autosomal dominant deafness 38', 'autosomal dominant nonsyndromic deafness type 6', 'WFS1 autosomal dominant nonsyndromic deafness', 'DFNA6', 'deafness, autosomal dominant 6/14/38']",0110584,600965,,C1833021,,,,C563421,,,,
mondo:0010964,"epiphyseal dysplasia, multiple, 3","['EDM3', 'epiphyseal dysplasia, multiple, type 3', 'COL9A3 multiple epiphyseal dysplasia (disease)', 'epiphyseal dysplasia multiple 3', 'multiple epiphyseal dysplasia 3', 'epiphyseal dysplasia, multiple, 3', 'epiphyseal dysplasia, multiple, 3, with or without myopathy', 'epiphyseal dysplasia, multiple, 3, with myopathy']",0070304,600969,,C1832998,,,,C535503,,,,
mondo:0010965,autosomal recessive nonsyndromic hearing loss 6,"['deafness, autosomal recessive 6', 'deafness, autosomal recessive type 6', 'DFNB6', 'autosomal recessive nonsyndromic deafness caused by mutation in TMIE', 'TMIE autosomal recessive nonsyndromic deafness', 'neurosensory nonsyndromic recessive deafness 6', 'autosomal recessive nonsyndromic deafness type 6', 'autosomal recessive nonsyndromic deafness 6', 'autosomal recessive deafness 6']",0110512,600971,,C1832992,,,,C563418,,,,
mondo:0010966,achondrogenesis type IB,"['achondrogenesis Fraccaro type', 'ACG1B', 'Fraccaro achondrogenesis', 'achondrogenesis, Parenti-Fraccaro type', 'achondrogenesis, type IB', 'achondrogenesis type 1B', 'achondrogenesis, type 1B', 'achondrogenesis Ib', 'achondrogenesis, Fraccaro type']",0080055,600972,93298,,"['-0.6045', '0.1199', '0.4321', '-0.2451', '0.2756', '-0.4268', '-0.12085', '0.4695', '-0.8687', '-0.01104', '-0.1034', '0.01906', '-0.03854', '-0.0244', '-0.515', '0.1406', '0.3884', '-0.0912', '-0.11536', '-0.6577', '-0.1246', '0.0369', '0.8677', '-0.1562', '-0.1381', '0.05957', '-0.0725', '0.03864', '0.3948', '-0.2783', '0.2817', '-0.1231', '0.611', '0.2512', '0.1902', '-0.145', '-0.264', '0.1539', '-0.0502', '-0.5645', '0.05106', '-0.469', '-0.225', '0.01269', '-0.1016', '-0.05035', '0.2161', '0.8296', '0.8003', '-0.1808', '0.2069', '-0.218', '0.2177', '0.2778', '-0.84', '-0.8916', '-0.3965', '0.01194', '-0.0736', '-0.2075', '0.2856', '0.00147', '-0.5425', '0.1659', '-0.2976', '-0.05576', '0.2534', '0.01736', '-0.527', '0.3533', '-0.1212', '0.062', '0.5938', '0.0759', '0.0681', '0.2947', '-0.3955', '0.0787', '-0.395', '-0.4883', '-0.2247', '-0.1018', '-0.15', '-0.10474', '-0.1934', '-0.1251', '-0.0903', '0.1671', '0.3772', '-0.2563', '-0.1681', '0.187', '0.243', '0.3997', '0.3843', '0.1482', '0.311', '-0.775', '0.4512', '0.1453']",,,,,,,
mondo:0010967,autosomal recessive nonsyndromic hearing loss 7,"['DFNB11', 'autosomal recessive nonsyndromic deafness caused by mutation in TMC1', 'autosomal recessive nonsyndromic deafness type 7', 'deafness, autosomal recessive type 7', 'DFNB7', 'autosomal recessive deafness 7', 'TMC1 autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive 11', 'deafness, autosomal recessive 7', 'autosomal recessive nonsyndromic deafness 7']",0110520,600974,,C1832978,,,,C563417,,,,
mondo:0010968,"glaucoma 3, primary infantile, B","['glaucoma 3 primary infantile B', 'GLC3B', 'glaucoma primary congenita type 3B', 'GLC3 type B', 'Glc3, type B', 'primary congenital glaucoma type 3B', 'glaucoma, primary congenital, type B', 'primary congenital glaucoma', 'glaucoma 3, primary infantile, B']",,600975,,C1832977,,,,C536824,,,,
mondo:0010969,cone-rod dystrophy 5,"['PITPNM3 cone-rod dystrophy', 'cone-rod dystrophy 5', 'cone-rod dystrophy caused by mutation in PITPNM3', 'cone-rod dystrophy type 5', 'CORD5']",0111010,600977,,C1832976,,,,C563415,,,,
mondo:0010970,"cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies","['cleft palate, CARDIAC defects, and mental retardation', 'cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies', 'cleft palate, CARDIAC defects, and intellectual disability', 'CPCMR', 'cleft palate, Cardiac defects, and intellectual disability', 'cleft palate, Cardiac defects, and mental retardation']",0111697,600987,,C1832950,,,,C563414,,,,
mondo:0010971,infundibulopelvic stenosis-multicystic kidney syndrome,['infundibulopelvic dysgenesis'],,600989,1849,C1832949,,,,C535528,,,,
mondo:0010972,hydrocephalus-costovertebral dysplasia-Sprengel anomaly syndrome,"['hydrocephalus, costovertebral dysplasia, and Sprengel anomaly', 'hydrocephalus, skeletal anomalies, and mental disturbance', 'Ferlini-Ragno-Calzolari syndrome', 'Waaler-Aarskog syndrome', 'hydrocephalus, Sprengel anomaly, and costovertebral dysplasia']",,600991,2180,,,,,C536461,,,,
mondo:0010973,autosomal dominant nonsyndromic hearing loss 5,"['autosomal dominant nonsyndromic deafness caused by mutation in GSDME', 'DFNA5', 'deafness, autosomal dominant type 5', 'autosomal dominant deafness 5', 'GSDME autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness 5', 'deafness, autosomal dominant 5', 'autosomal dominant nonsyndromic deafness type 5']",0110575,600994,,C1832932,,,,C563410,,,,
mondo:0010974,"nephrotic syndrome, type 2","['SRN1', 'nephrotic syndrome, idiopathic, steroid-resistant', 'NPHS2 nephrotic syndrome', 'nephrotic syndrome, type 2', 'NPHS2', 'nephrotic syndrome caused by mutation in NPHS2', 'nephrotic syndrome, steroid-resistant, autosomal recessive']",0080379,600995,,,,,,,,,,
mondo:0010976,"epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive","['EBS-AR KRT14', 'epidermolysis bullosa simplex, autosomal recessive 1', 'KRT14-related autosomal recessive epidermolysis bullosa simplex', 'epidermolysis bullosa simplex, autosomal recessive K14', 'KRT14-related epidermolysis bullosa simplex', 'epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive', 'EBSB1', 'EBS, autosomal recessive K14', 'KRT14-related autosomal recessive EBS', 'epidermolysis bullosa simplex, autosomal recessive type 1']",,601001,89838,,"['0.883', '-0.2479', '-0.1421', '-0.244', '0.02686', '-0.639', '-0.625', '0.3984', '-0.1595', '-0.668', '0.1729', '-0.256', '-0.8394', '0.3125', '-0.6284', '0.03906', '0.3723', '-1.145', '-0.5386', '-1.072', '-0.3687', '-0.09357', '0.4028', '0.363', '0.3098', '0.2893', '-0.926', '0.5786', '-0.37', '-0.844', '0.1892', '-0.07166', '-0.4075', '-0.001982', '-0.07477', '0.1993', '-1.18', '-0.0729', '0.911', '-0.6396', '0.2413', '-0.565', '0.11615', '0.1609', '0.09534', '-0.3086', '-0.306', '0.1486', '0.4248', '-0.188', '-0.4897', '-0.517', '0.5386', '0.03726', '-0.07', '-0.5107', '-0.2698', '1.188', '-0.799', '-0.2466', '-0.0114', '0.353', '0.01973', '0.01457', '0.9307', '0.7656', '0.379', '0.347', '-0.867', '0.3289', '-0.072', '0.0626', '-0.3462', '-0.02307', '-0.09735', '0.001636', '-0.035', '0.2297', '0.04233', '-0.3125', '-0.989', '0.2242', '-0.3418', '-0.2627', '0.3674', '0.3354', '-0.9175', '0.7964', '1.12', '0.481', '-0.5015', '0.2866', '0.00506', '0.4558', '0.04242', '0.8325', '0.1986', '-0.4907', '0.9062', '0.1649']",,,C563408,,,,
mondo:0010977,Brody myopathy,"['sarcoplasmic reticulum -Ca2+ATPase deficiency', 'Brody disease', 'Brody myopathy']",0050692,601003,53347,C1832918,"['-0.2795', '-0.0486', '-0.526', '-0.2303', '-0.5303', '-0.6494', '0.2432', '0.0664', '-0.5005', '-0.3296', '0.1534', '0.4521', '0.07574', '0.1818', '-0.0528', '0.423', '-0.363', '-0.0753', '-0.3386', '-0.482', '0.1545', '-0.1544', '0.2466', '0.318', '-0.1355', '0.16', '-0.06384', '-0.1473', '-0.3079', '0.0404', '0.285', '-0.03574', '0.01226', '0.1989', '0.00946', '-0.529', '-0.05695', '-0.2764', '0.725', '-0.2683', '-0.0613', '-0.6724', '-0.1409', '0.05145', '0.3313', '-0.2042', '-0.1173', '0.4006', '0.281', '0.504', '-0.2854', '-0.0743', '0.2239', '-0.0523', '0.02849', '-0.2402', '0.4382', '0.005802', '-0.1681', '0.2742', '0.243', '-0.1663', '0.4404', '-0.3965', '-0.1844', '0.10614', '0.5024', '0.428', '0.2793', '0.36', '-0.03525', '-0.148', '0.00557', '0.0633', '0.6465', '0.708', '0.00975', '0.3557', '0.2301', '0.01782', '0.4263', '0.2377', '0.363', '-0.1965', '0.2793', '0.229', '-0.01261', '0.0829', '0.3442', '0.1832', '0.0626', '-0.486', '-0.078', '0.0717', '0.681', '0.1663', '0.2345', '-0.2522', '-0.426', '-0.336']",,,C536607,359.89,,,
mondo:0010978,"portal vein, cavernous transformation of","['portal vein, cavernous transformation of']",,601004,,C1832917,,,,C563407,,,,
mondo:0010979,Timothy syndrome,"['long QT syndrome-syndactyly syndrome', 'long QT syndrome 8', 'TIMOTHY syndrome', 'LQT8', 'Timothy syndrome', 'TS', 'long QT syndrome type 8', 'long QT syndrome with syndactyly']",0060173,601005,65283,C1832916,"['0.5347', '-0.4668', '-0.03023', '-0.2966', '0.3628', '0.1422', '1.05', '1.119', '-0.2878', '-0.0447', '0.07104', '-0.02925', '0.02396', '0.4216', '-0.6743', '0.07007', '-0.6465', '-0.1627', '-0.0918', '-0.5547', '0.59', '-0.01113', '0.49', '-0.11365', '0.682', '-0.5723', '-0.0695', '0.523', '0.8853', '-0.546', '0.5913', '-0.05945', '0.2441', '0.3386', '-0.5825', '-0.366', '-0.0322', '0.02841', '-0.373', '-0.2273', '0.2201', '-0.0728', '0.1859', '0.001655', '0.8', '-0.01293', '-0.02962', '0.709', '-0.2223', '0.325', '-0.5454', '0.09827', '-0.2822', '0.6196', '0.01738', '-0.2048', '-0.2766', '0.1803', '0.3464', '0.1714', '-0.09265', '0.3743', '0.5186', '0.1758', '-0.2361', '0.06647', '0.4517', '-0.0607', '0.2157', '0.789', '-0.3662', '0.0627', '-0.13', '-0.248', '0.03506', '-0.076', '0.6055', '-0.4712', '-0.582', '-0.01103', '0.358', '0.1101', '0.1675', '-0.0192', '-0.0839', '0.5225', '0.0413', '0.277', '0.241', '-0.2393', '-0.163', '0.1702', '0.1355', '0.2705', '-0.127', '0.4297', '0.4128', '-0.705', '0.09656', '0.6997']",C142894,,C536962,,,,
mondo:0010980,"midline malformations, multiple, with limb abnormalities and hypopituitarism","['Dincsoy-Salih-Patel syndrome', 'midline malformations, multiple, with limb abnormalities and hypopituitarism', 'Dincsoy syndrome']",,601016,1678,C1832874,,,,C536177,,,,
mondo:0010981,absent tibia-polydactyly-arachnoid cyst syndrome,"['tibia absent polydactyly arachnoid cyst', 'tibia, absence or hypoplasia of, with polydactyly, RETROCEREBELLAR arachnoid cyst, and other anomalies', 'Holmes-Collins syndrome', 'tibia, absence or hypoplasia of, with polydactyly, retrocerebellar arachnoid cyst, and other anomalies', 'Holmes Collins syndrome', 'absence/hypoplasia of tibia, polydactyly, retrocerebellar arachnoid cyst, and other anomalies']",,601027,3328,,,,,C563403,,,,
mondo:0010982,ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin,"['ichthyosis-intellectual disability syndrome with large keratohyalin granules in the skin', 'ichthyosis-mental retardation syndrome with large keratohyalin granules in the skin']",,601039,,C1832858,,,,C563402,,,,
mondo:0010983,dystonia 9,"['dystonia type 9', 'dystonia 9', 'DYT9', 'choreoathetosis/spasticity, episodic', 'Cse choreoathetosis, paroxysmal, with episodic ataxia', 'paroxysmal dystonic choreathetosis with episodic ataxia and spasticity', 'choreoathetosis, kinesigenic, with episodic ataxia and spasticity', 'episodic choreoathetosis/spasticity']",0090044,601042,53583,C1832855,"['0.4397', '0.1777', '-0.336', '-0.2242', '-0.296', '-1.425', '0.5103', '0.02306', '-0.957', '0.2893', '0.7524', '0.9023', '-0.06305', '0.1921', '0.854', '0.0941', '-0.05307', '-0.506', '-0.4438', '-0.752', '-0.1621', '0.04095', '-0.3647', '-0.253', '-0.156', '0.006172', '-0.3665', '-0.13', '-0.04874', '0.2034', '0.2089', '0.6147', '0.903', '-0.184', '0.3523', '-0.1393', '0.1942', '0.01886', '0.422', '-0.578', '0.645', '-0.407', '-0.3586', '0.11176', '0.3384', '-0.19', '-0.4546', '0.1531', '0.5786', '0.3455', '-0.12195', '0.3765', '0.6646', '0.0009136', '0.583', '0.01295', '0.342', '0.653', '0.10455', '-0.2119', '-0.554', '-0.10583', '0.4636', '-0.6646', '-1.086', '0.65', '0.61', '0.3281', '-0.3625', '0.2666', '-0.4175', '-0.01797', '0.0778', '-0.3035', '0.1997', '0.615', '0.772', '0.1748', '0.2284', '-0.08875', '-0.12354', '0.1079', '0.4146', '0.3608', '1.061', '0.1598', '-0.01017', '0.502', '1.338', '0.137', '0.3264', '0.1841', '0.4565', '0.143', '0.88', '-0.08014', '-0.4766', '0.1096', '0.3774', '-0.3613']",,,C563401,,,,
mondo:0010984,Usher syndrome type 1D,"['USH1D', 'Usher syndrome, type Id/F, Cdh23/Pcdh15, digenic', 'Usher syndrome, type 1D/F digenic', 'Ush1D/F, Cdh23/Pcdh15, digenic', 'USHER syndrome, type ID', 'Usher syndrome type ID', 'Usher syndrome, type 1D']",0110831,601067,,,,,,,,H35.5,,
mondo:0010985,"epilepsy, familial adult myoclonic, 1","['epilepsy, familial ADULT myoclonic, 1', 'FAME1', 'benign adult familial myoclonic epilepsy 1', 'cortical myoclonic tremor with epilepsy, familial, 1']",0111690,601068,,C1832841,,,,C563399,,,,
mondo:0010986,autosomal recessive nonsyndromic hearing loss 9,"['NRSD9', 'auditory neuropathy, autosomal recessive, 1', 'deafness, autosomal recessive type 9', 'neurosensory nonsyndromic recessive deafness 9', 'OTOF autosomal recessive nonsyndromic deafness', 'auditory neuropathy, nonsyndromic recessive', 'autosomal recessive deafness 9', 'autosomal recessive nonsyndromic deafness type 9', 'autosomal recessive nonsyndromic deafness caused by mutation in OTOF', 'DFNB9', 'autosomal recessive nonsyndromic deafness 9', 'deafness, autosomal recessive 9']",0110535,601071,,,,,,,,,,
mondo:0010987,autosomal recessive nonsyndromic hearing loss 8,"['autosomal recessive deafness 10', 'deafness, autosomal recessive 8', 'DFNB8', 'deafness, autosomal recessive type 8', 'DFNB10', 'deafness, autosomal recessive 8/10', 'deafness, childhood-onset neurosensory, autosomal recessive 8', 'autosomal recessive nonsyndromic deafness type 8', 'NRSD8', 'autosomal recessive deafness 8', 'childhood-onset neurosensory autosomal recessive deafness 8', 'deafness, autosomal recessive 10', 'autosomal recessive nonsyndromic deafness 8', 'neurosensory nonsyndromic recessive deafness 8']",0110527,601072,,C1832827,,,,,,,,
mondo:0010988,aplasia cutis-myopia syndrome,"['Gershoni-Baruch-Leibo syndrome', 'aplasia cutis congenita, high myopia, and cone-rod dysfunction', 'aplasia cutis myopia']",,601075,1117,,,,,C563394,,,,
mondo:0010989,Mayer-Rokitansky-Küster-Hauser syndrome type 2,"['MULLERIAN duct aplasia, unilateral renal agenesis, and cervicothoracic somite anomalies', 'Mullerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome', 'Müllerian duct aplasia-renal dysplasia-cervical somite anomalies syndrome', 'Klippel-Feil deformity, conductive deafness, and absent vagina', 'atypical MRKH syndrome', 'Mayer-Rokitansky-Küster-Hauser syndrome type 2', 'MRKH, type 2', 'MURCS association', 'MRKH syndrome type 2', 'Mayer-Rokitansky-Kuster-Hauser syndrome, type 2', 'MURCS']",0112179,601076,2578,,,,,,,,,
mondo:0010991,"laterality defects, autosomal dominant","['laterality defects, autosomal dominant', 'laterality defects dominant']",,601086,,C1832813,,,,C563391,,,,
mondo:0010992,Ayme-Gripp syndrome,"['AYGRP', 'Ayme-Gripp syndrome', 'cataracts, congenital, with sensorineural deafness, Down syndrome-like Facial appearance, short stature, and mental retardation', 'AYME-Gripp syndrome', 'Aymé-Gripp syndrome', 'cataracts, congenital, with sensorineural deafness, Down syndrome-like Facial appearance, short stature, and intellectual disability']",0111688,601088,477668,C1832812,"['-0.01738', '0.03647', '0.01026', '-0.02257', '0.01634', '-0.06885', '0.00633', '0.04218', '-0.03424', '-0.03897', '-0.01245', '-0.01015', '-7.87e-06', '0.0175', '-0.02594', '-0.02484', '-0.00503', '-0.00337', '-0.0086', '-0.0858', '-0.006683', '-0.02435', '0.02419', '-0.02776', '0.008316', '-0.009094', '-0.03125', '-0.001258', '0.02356', '-0.03473', '0.03378', '-0.01799', '0.03592', '0.02473', '0.01035', '-0.007965', '-0.01361', '-0.0172', '-0.015366', '-0.0409', '0.01029', '-0.03397', '0.00917', '-0.02324', '0.004745', '-0.0515', '-0.0341', '0.02893', '0.01851', '0.01472', '-0.01736', '-0.006226', '-0.00731', '-0.00987', '-0.0421', '-0.007465', '0.02141', '-0.00324', '-0.04312', '0.01164', '0.03122', '0.01825', '0.0224', '0.02943', '-0.013535', '0.01093', '0.0519', '0.02063', '-0.0386', '0.05756', '-0.03488', '0.01483', '0.01962', '-0.02376', '0.01822', '0.00931', '0.006504', '0.0116', '-0.02074', '-0.00523', '-0.00824', '0.02103', '-0.009026', '0.04755', '-0.01357', '0.001549', '0.01362', '0.06082', '0.0593', '0.004803', '0.01672', '0.0354', '0.01707', '0.00884', '0.08105', '0.0307', '0.04477', '-0.07513', '-0.01715', '0.01685']",,0009020,C563390,,,,
mondo:0010993,Harrod syndrome,"['craniofacial digital genital anomalies', 'Harrod Doman Keele syndrome', 'Harrod syndrome', 'cranio-facio-digito-genital syndrome']",,601095,2115,C0795970,,,,C535635,,,,
mondo:0010995,Charcot-Marie-Tooth disease type 1C,"['CMT 1C', 'Charcot-Marie-Tooth neuropathy type 1C', 'CMT1C', 'Charcot-Marie-Tooth disease, demyelinating, type 1C', 'Charcot Marie Tooth disease type 1C', 'LITAF Charcot-Marie-Tooth disease type 1', 'Charcot-Marie-Tooth neuropathy, type 1C', 'neuropathy, hereditary motor and sensory, type 1C', 'CMT, slow nerve conduction type C', 'Charcot-Marie-Tooth disease, type 1C', 'Charcot-Marie-Tooth disease type 1 caused by mutation in LITAF', 'HMSN IC', 'HMSN1C', 'neuropathy hereditary motor and sensory type 1C', 'CMT slow nerve conduction type C', 'HMSN 1C']",0110151,601098,101083,C0270913,"['0.0662', '0.3535', '0.1177', '-0.165', '-0.1321', '-0.1786', '-0.2988', '0.554', '-0.828', '0.2048', '0.1249', '0.09155', '-0.2432', '0.2426', '-0.01672', '-0.273', '-0.1531', '-0.6294', '-0.3303', '-0.633', '-0.06946', '0.1558', '0.5786', '0.7373', '0.314', '0.601', '0.03027', '0.11743', '0.07947', '-0.1807', '-0.1096', '-0.6436', '0.3254', '0.3538', '0.1835', '-0.7954', '-0.547', '-0.167', '0.3115', '-0.2164', '-1.362', '-0.4866', '-0.505', '0.644', '0.1231', '-0.2289', '-0.11066', '0.015434', '-0.1152', '0.2295', '0.1691', '0.2998', '-0.4473', '-0.986', '0.287', '-0.2205', '0.03964', '0.16', '-0.4788', '0.0004606', '-0.4075', '0.2817', '0.8823', '1.044', '-0.744', '1.123', '-0.1666', '0.6377', '-0.656', '0.4128', '-0.9824', '0.1449', '0.5884', '-0.4392', '0.8315', '0.549', '-0.1627', '0.2145', '0.4622', '-0.06433', '-0.05054', '-0.1754', '0.86', '0.594', '0.1293', '-0.007584', '0.0744', '0.5674', '0.601', '0.535', '0.1526', '-0.3745', '0.4553', '0.3638', '0.5093', '0.581', '0.554', '-0.595', '-0.3223', '0.6167']",,,C537984,,,,
mondo:0010996,hereditary hemorrhagic telangiectasia type 3,"['telangiectasia, hereditary hemorrhagic, type 3', 'telangiectasia hereditary hemorrhagic type 3', 'Osler Weber Rendu syndrome type 3', 'ORW3', 'HHT3']",,601101,,,,,,C537140,,,,
mondo:0010997,"supranuclear palsy, progressive, 1","['Steele-Richardson-Olszewski disease', 'PSNP1', 'Richardson syndrome', 'PSP', 'supranuclear palsy, progressive, 1', 'classic PSP syndrome', 'supranuclear palsy, progressive', 'supranuclear palsy, progressive, type 1', 'classic progressive supranuclear palsy syndrome', 'Steele-Richardson-Olszewski syndrome']",,601104,240071,CN201679,"['0.4275', '1.114', '0.1177', '0.0371', '-0.576', '-0.5635', '0.5005', '0.3455', '-1.01', '0.05655', '0.851', '-0.10284', '-0.5195', '0.6626', '0.2146', '-0.1608', '-0.2957', '-0.664', '-0.535', '-0.3105', '0.04773', '-0.02437', '-0.2935', '0.004135', '0.264', '0.08264', '0.4014', '-0.1403', '-0.494', '1.069', '0.2388', '-0.04327', '0.163', '-0.11206', '0.2568', '-0.251', '0.6235', '0.05783', '-0.07666', '-0.911', '0.897', '-0.256', '-0.072', '0.3186', '0.482', '-0.3904', '0.04733', '-0.1499', '0.2296', '0.6475', '0.2163', '0.453', '0.000883', '-1.243', '0.07996', '-0.5845', '-0.268', '-0.2356', '-0.1442', '-0.1852', '0.2617', '-0.345', '-0.4053', '-0.401', '-0.2118', '0.5312', '0.2301', '-0.001181', '-0.2512', '1.024', '-0.2646', '-0.3984', '-0.01164', '-0.7783', '0.4956', '0.5034', '-0.03604', '0.113', '-0.03467', '0.4976', '0.3943', '-1.634', '-0.03223', '0.868', '0.0476', '-0.414', '0.1729', '-0.153', '0.5273', '-0.6665', '0.4846', '0.277', '-0.587', '0.928', '0.2352', '0.9385', '0.010475', '-0.4392', '0.5513', '0.2205']",,,,,,,
mondo:0010998,ALG3-congenital disorder of glycosylation,"['CDG Id', 'mannosyltransferase 6 deficiency', 'carbohydrate-deficient glycoprotein syndrome, type IV, formerly', 'CDG-Id', 'congenital disorder of glycosylation, type Id', 'ALG3-CDG', 'CDG syndrome type Id', 'congenital disorder of glycosylation type 1d', 'congenital disorder of glycosylation type Id', 'CDG 1D', 'CDGId', 'CDGS, type IV, formerly', 'carbohydrate-deficient glycoprotein syndrome type IV (formerly)', 'CDGS, type IV', 'carbohydrate deficient glycoprotein syndrome type Id', 'CDGS4 (formerly)', 'CDG1D', 'ALG3-CDG (CDG-Id)', 'carbohydrate-deficient glycoprotein syndrome, type IV']",0080556,601110,79321,C1832736,"['-0.5283', '0.0819', '0.4521', '-0.2693', '0.109', '-0.4546', '-0.2029', '0.3022', '-0.8003', '-0.2627', '-0.01141', '-0.3303', '-0.2197', '-0.432', '-0.3044', '-0.01121', '0.3113', '-0.3103', '-0.3064', '-0.5293', '0.2532', '-0.175', '-0.09015', '0.1755', '0.2393', '-0.04456', '-0.1952', '0.0429', '0.1652', '-0.2472', '0.2028', '0.1543', '0.6504', '0.1115', '-0.04645', '-0.067', '-0.2283', '0.02028', '-0.1614', '-0.3005', '-0.0123', '-0.55', '0.1334', '0.2585', '-0.1891', '-0.1935', '0.03354', '0.2515', '0.1896', '-0.0635', '-0.2245', '0.2247', '-0.1256', '-0.1454', '-0.1534', '-0.4429', '0.222', '0.2366', '-0.11456', '0.3198', '-0.0193', '-0.0394', '0.0679', '0.04205', '-0.09467', '-0.06445', '0.1722', '0.2893', '-0.279', '0.1812', '-0.4324', '0.4844', '0.3655', '0.0915', '-0.1884', '0.3', '0.631', '-0.0683', '-0.1703', '0.2244', '0.4163', '-0.1891', '-0.277', '0.5073', '-0.1957', '0.02469', '-0.0835', '0.522', '0.0989', '0.356', '-0.0577', '0.371', '0.2365', '0.00381', '0.472', '0.1879', '0.557', '-0.04053', '0.543', '0.566']",C126870,,C535742,,,,
mondo:0010999,fallot complex-intellectual disability-growth delay syndrome,"['Bindewald Ulmer Muller syndrome', 'FALLOT complex with severe mental and growth retardation', 'Bindewald-Ulmer-Müller syndrome']",,601127,3304,C1832735,,,,C536608,,,,
mondo:0011000,guanylate cyclase 2E,"['guanylyl cyclase, Membrane, type E', 'guanylate cyclase type 2E', 'GUCY2EP', 'guanylate cyclase 2E, pseudogene', 'Gucy2D, mouse, homolog of', 'GUCY2E', 'guanylate cyclase 2E', 'GC-E']",,601138,,,,,,,,,,
mondo:0011001,Brugada syndrome 1,"['sudden unexplained nocturnal death syndrome', 'Brugada syndrome caused by mutation in SCN5A', 'BRGDA1', 'Cardiac conduction defect, nonspecific', 'Brugada syndrome 1', 'Brugada syndrome type 1', 'right bundle branch block, St segment elevation, and sudden death syndrome', 'SCN5A Brugada syndrome']",0110218,601144,,CN029323,,,,,,,,
mondo:0011002,"neuropathy, hereditary motor and sensory, type 6A","['neuropathy, hereditary motor and sensory, type VIA', 'HMSN 6A', 'Charcot-Marie-Tooth disease, type 6', 'hereditary motor and sensory neuropathy VIA', 'hereditary motor and sensory neuropathy type 6 caused by mutation in MFN2', 'Charcot-Marie-Tooth disease, type 6A', 'MFN2 hereditary motor and sensory neuropathy type 6', 'neuropathy, hereditary motor and sensory, type 6', 'peripheral neuropathy and optic atrophy', 'HMSN6A']",,601152,,,,,,,,,,
mondo:0011003,dilated cardiomyopathy 1E,"['cardiomyopathy dilated with conduction defect type 2', 'dilated cardiomyopathy with conduction defect 2', 'CMD1E', 'SCN5A familial isolated dilated cardiomyopathy', 'cardiomyopathy, dilated, with conduction defect 2', 'familial isolated dilated cardiomyopathy caused by mutation in SCN5A', 'cardiomyopathy, dilated, type 1E', 'cardiomyopathy, dilated, with conduction disorder and arrhythmia', 'dilated cardiomyopathy with conduction disorder and arrhythmia', 'dilated cardiomyopathy type 1E', 'cardiomyopathy, dilated, 1E', 'CDCD2']",0110433,601154,,C1832680,,,,C563384,,,,
mondo:0011004,lissencephaly type 3-metacarpal bone dysplasia syndrome,"['lissencephaly type 3 and bone dysplasia', 'lissencephaly type III and bone dysplasia']",,601160,86822,C1832678,,,,C563383,,,,
mondo:0011005,trisomy 18-like syndrome,['trisomy 18-like syndrome'],,601161,,C1832677,,,,C563382,,,,
mondo:0011006,hereditary spastic paraplegia 9A,"['AD-SPG9A', 'spastic paraparesis with amyopathy, cataracts, and gastroesophageal reflux', 'spastic paraplegia 9A, autosomal dominant', 'SPG9A', 'spastic paraparesis with amyopathy, cataracts and gastroesophageal reflux', 'autosomal dominant complex spastic paraplegia type 9A', 'hereditary spastic paraplegia type 9A', 'cataracts motor neuropathy-short stature-skeletal anomalies syndrome', 'cataracts with motor neuronopathy, short stature and skeletal abnormalities', 'spastic paraparesis with amyotrophy, cataracts, and gastroesophageal reflux', 'cataracts with motor neuronopathy, short stature, and skeletal abnormalities', 'autosomal dominant spastic paraplegia 9A']",0110824,601162,447753,CN237701,,,,C536868,,,,
mondo:0011007,diaphragmatic defect-limb deficiency-skull defect syndrome,"['froster-Huch syndrome', 'froster syndrome', 'diaphragmatic defect limb deficiency skull defect', 'diaphragmatic defects, limb deficiencies, and ossification defects of skull']",,601163,2141,,,,,C563380,,,,
mondo:0011008,cleft lip/palate-intestinal malrotation-cardiopathy syndrome,"['cleft lip, cleft palate, characteristic facies, intestinal malrotation, and lethal congenital heart disease', 'McPherson Clemens syndrome', 'cleft LIP/palate with characteristic facies, intestinal malrotation, and lethal congenital heart disease', 'McPherson-Clemens syndrome']",,601165,2001,C2931750,,,,C538160,,,,
mondo:0011009,"muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers","['muscular dystrophy, congenital, with severe central nervous system atrophy and absence of large myelinated fibers']",,601170,,C1832665,,,,C563378,,,,
mondo:0011010,Matthew-Wood syndrome,"['anophthalmia/microphthalmia and pulmonary hypoplasia', 'microphthalmia, syndromic type 9', 'microphthalmia syndromic type 9', 'anophthalmia-pulmonary hypoplasia syndrome', 'syndromic microphthalmia type 9', 'clinical anophthalmia mild facial dysmorphism lung heart and diaphragm malformations', 'microphthalmia, isolated, with coloboma 8', 'Matthew-Wood syndrome', 'microphthalmia syndromic 9', 'Matthew Wood syndrome', 'pulmonary Hypoplasia-diaphragmatic hernia-anophthalmia-Cardiac defect', 'anophthalmia, clinical, with mild Facial Dysmorphism and variable malformations of the lung, heart, and diaphragm', 'pulmonary agenesis microphthalmi and diaphragmatic defect', 'MCOPS9', 'spear syndrome', 'microphthalmia, syndromic 9', 'pulmonary agenesis, microphthalmia, and diaphragmatic defect']",0111807,601186,98938,C1832661,"['-0.2952', '-0.2842', '-0.05035', '0.3262', '-0.0894', '-0.4846', '-0.1285', '0.2693', '-0.5527', '-0.7363', '-0.4019', '-0.3452', '0.3406', '0.2406', '0.04034', '-0.1489', '-0.1427', '-0.1506', '-0.2361', '-0.4434', '-0.1935', '0.6016', '0.498', '-0.7153', '0.4236', '0.2428', '-0.04382', '0.7285', '0.435', '-0.4597', '0.758', '-0.1635', '-0.0694', '0.02515', '0.0922', '0.03793', '0.2566', '-0.4766', '0.05927', '-0.06165', '0.2489', '0.1355', '0.2162', '-0.307', '0.07336', '-0.41', '-0.137', '0.1709', '-0.8296', '-0.11786', '-0.3298', '-0.07635', '-0.1565', '0.2764', '-0.2673', '-0.688', '0.1205', '0.1693', '-0.3215', '0.434', '-0.1758', '-0.1262', '0.1422', '0.3677', '-0.281', '-0.636', '0.01474', '0.2422', '-0.743', '0.638', '0.329', '0.47', '0.2622', '-0.2343', '-0.1594', '-0.01329', '0.1218', '-0.186', '-0.02719', '-0.07074', '-0.5557', '0.442', '0.617', '0.453', '-0.00615', '-0.4338', '0.02562', '0.2947', '-0.3115', '-0.335', '0.11664', '0.1362', '0.4893', '-0.3013', '1.355', '-0.10516', '0.06805', '-0.3806', '-0.04044', '-0.1332']",,,C537768,,,,
mondo:0011011,skeletal dysplasia-epilepsy-short stature syndrome,"['GURRIERI syndrome', 'mental retardation, epilepsy, short stature and skeletal dysplasia', 'Gurrieri-Sammito-Bellussi syndrome', 'intellectual disability, epilepsy, short stature and skeletal dysplasia']",,601187,1858,C0796046,,,,C537625,,,,
mondo:0011012,African iron overload,"['hereditary iron overload and African Americans', 'African iron overload', 'iron overload in Africa', 'Bantu siderosis']",0111033,601195,139507,,,,,C537904,,,,
mondo:0011013,autosomal dominant hypocalcemia 1,"['CASR autosomal dominant hypocalcemia', 'autosomal dominant hypocalcemia caused by mutation in CASR', 'hypocalcemia, autosomal dominant 1', 'autosomal dominant hypocalcemia type 1', 'hypocalcemia, autosomal dominant', 'hypocalcemia, autosomal dominant type 1', 'hypercalciuric hypocalcemia', 'hypocalcemia, familial', 'hypocalcemia, autosomal dominant 1, with Bartter syndrome', 'HYPOC1', 'hypocalcemia, autosomal dominant, with Bartter syndrome']",0090107,601198,263417,C3715128,"['-0.1211', '0.1875', '0.1963', '-0.2072', '-0.226', '0.0531', '-0.288', '0.1984', '-0.1437', '-0.1576', '-0.3347', '-0.1189', '0.2372', '-0.02718', '-0.161', '-0.2869', '0.08954', '0.1327', '0.3098', '-0.613', '0.0176', '-0.2435', '0.4053', '0.1759', '0.3672', '0.3706', '0.04962', '-0.2423', '0.2595', '-0.2844', '0.00438', '0.3237', '0.3928', '0.2905', '-0.2428', '-0.07117', '0.2072', '0.2152', '-0.0627', '-0.4592', '-0.07654', '-0.156', '0.4385', '-0.3298', '0.0727', '-0.3833', '-0.11774', '0.4043', '0.1271', '0.0959', '0.05212', '0.0461', '0.269', '-0.3374', '-0.2778', '0.02786', '0.1848', '-0.5146', '-0.2588', '0.274', '0.1733', '0.157', '0.0644', '-0.3125', '0.10583', '-0.1559', '0.0589', '0.254', '-0.3762', '0.2452', '-0.3948', '0.04663', '0.3389', '-0.1587', '0.199', '0.1726', '-0.05286', '-0.164', '-0.01449', '0.002474', '-0.0692', '0.1448', '-0.2214', '0.1508', '-0.0835', '0.31', '0.227', '0.04495', '0.414', '0.1076', '0.1783', '0.0476', '0.02634', '-0.1831', '0.4956', '0.1521', '0.2761', '-0.2803', '-0.2079', '0.208']",,,,,,,
mondo:0011014,pleuropulmonary blastoma,"['pleuropulmonary blastoma (morphologic abnormality)', 'PPB', 'PPB familial tumor and dysplasia syndrome', 'childhood pulmonary blastoma', 'pediatric pulmonary blastoma', 'pleuropulmonary blastoma', 'PPB familial tumour and dysplasia syndrome', 'pulmonary blastoma of childhood', 'paediatric pulmonary blastoma']",4769,601200,64742,CN072455,"['0.3525', '-0.006725', '-0.2491', '-0.214', '0.1952', '-0.216', '0.4187', '-0.1431', '-0.536', '-0.0638', '-0.0651', '0.02344', '-0.3638', '-0.04663', '0.09357', '-0.09424', '-0.1285', '-0.5107', '-0.1252', '-0.1296', '0.01243', '-0.2817', '0.757', '-0.5923', '0.256', '-0.2454', '-0.1249', '-0.2223', '0.01474', '-0.375', '0.8105', '-0.3325', '0.437', '0.00399', '0.4824', '-0.3794', '-0.6133', '-0.09485', '-0.16', '0.0895', '0.02425', '-0.04416', '0.3262', '-0.1266', '-0.06464', '0.2722', '-0.1812', '0.01955', '0.003624', '0.10767', '0.06238', '-0.0548', '0.0105', '0.1007', '-0.1486', '0.1323', '0.1978', '0.05762', '-0.244', '0.3467', '0.497', '0.07324', '0.000601', '0.3079', '-0.2494', '-0.0471', '0.2241', '0.4558', '0.06323', '0.3506', '-0.10596', '0.1415', '0.04395', '-0.0939', '0.1577', '-0.1952', '-0.4006', '0.273', '-0.3682', '-0.542', '-0.279', '0.09436', '0.04822', '0.1678', '-0.8335', '-0.402', '0.596', '0.1921', '0.063', '-0.0247', '0.0328', '-0.1825', '0.02145', '-0.3545', '0.892', '0.1351', '0.4702', '-0.2152', '-0.2211', '0.011475']",C5669,0009052,C537516,162.9,,,
mondo:0011015,cataract 24,"['anterior polar cataract 24', 'anterior polar cataract 2', 'cataract 24', 'CTRCT24', 'CTAA2', 'cataract 24, anterior polar', 'cataract, anterior polar, 2', 'cataract type 24']",0110257,601202,,C1832609,,,,C537774,,,,
mondo:0011016,type 1 diabetes mellitus 11,"['IDDM11', 'diabetes mellitus, insulin-dependent, 11', 'insulin-dependent diabetes mellitus 11']",0110750,601208,,C1832605,,,,C563371,,,,
mondo:0011017,Naxos disease,"['wooly hair palmoplantar keratoderma cardiac abnormalities', 'keratoderma with wooly hair type I', 'keratoderma with woolly hair type I', 'cardiomyopathy, arrhythmogenic right ventricular, with skin, hair, and nail abnormalities', 'palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and wooly hair', 'keratosis palmoplantaris with arrythmogenic cardiomyopathy', 'keratosis palmoplantaris arrythmogenic cardiomyopathy woolly hair', 'wooly hair, palmoplantar keratoderma, and Cardiac abnormalities', 'palmoplantar hyperkeratosis with arrythmogenic cardiomyopathy', 'NAXOS disease', 'keratosis palmoplantaris with arrhythmogenic cardiomyopathy', 'Mal De Naxos', 'palmoplantar keratoderma with arrythmogenic cardiomyopathy', 'KWWH type I', 'NXD', 'palmoplantar keratoderma with arrhythmogenic right ventricular cardiomyopathy and woolly hair', 'keratosis palmoplantaris arrythmogenic cardiomyopathy wooly hair', 'woolly hair, palmoplantar keratoderma, and Cardiac abnormalities', 'woolly hair palmoplantar keratoderma cardiac abnormalities', 'Naxos disease']",0080551,601214,34217,C1832600,"['0.11206', '0.699', '-0.597', '0.06274', '0.3179', '-1.2', '0.142', '0.4634', '0.5684', '-0.595', '0.12085', '-0.1517', '-0.2507', '0.2128', '-0.5723', '0.00783', '-0.658', '-0.3936', '0.1936', '-1.055', '0.1597', '0.1305', '0.8555', '-0.9204', '0.1766', '-0.00919', '0.2666', '0.744', '-0.1642', '-0.0015545', '1.1045', '0.1027', '-0.417', '-0.357', '-0.0869', '-0.3398', '0.562', '0.1722', '-0.369', '-0.625', '0.07666', '-0.1254', '0.7993', '-0.1859', '-0.0886', '0.5415', '-0.9575', '0.2886', '-0.2488', '0.01201', '-0.4622', '0.4285', '0.1964', '0.03183', '0.3223', '-0.904', '0.63', '-0.1436', '-0.09265', '-0.0664', '0.07196', '0.2026', '0.0778', '-0.0862', '-0.2439', '0.4934', '0.936', '0.635', '-0.475', '0.1962', '-0.609', '-0.3943', '0.6304', '0.8237', '0.09375', '0.212', '-0.6094', '-0.345', '-0.0836', '0.4878', '0.5454', '0.1666', '0.1969', '-0.1377', '0.2018', '-0.473', '0.3264', '-0.03137', '0.35', '0.2272', '0.488', '-0.1055', '0.3596', '0.8994', '0.6523', '0.1256', '0.6816', '-0.5386', '0.0893', '-0.2852']",,,C538346,,,,
mondo:0011018,brachyolmia-amelogenesis imperfecta syndrome,"['DASS', 'tooth agenesis, selective, 6', 'selective tooth agenesis 5', 'amelogenesis imperfecta and platyspondyly', 'tooth agenesis, selective, 6, formerly', 'Verloes Bourguignon syndrome', 'skeletal dysplasia with amelogenesis imperfecta and platyspondyly', 'Verloes-Bourguignon syndrome', 'STHAG6', 'platyspondyly with amelogenesis imperfecta', 'platyspondyly-amelogenesis imperfecta syndrome', 'dental anomalies and short stature']",0090143,601216,2899,,"['-0.4106', '0.5146', '0.5547', '-0.6055', '0.367', '-0.303', '0.1376', '0.3843', '-0.6465', '-0.2183', '-0.1509', '0.03265', '-0.2423', '-0.07776', '0.0512', '0.09937', '0.5415', '-0.02336', '-0.1573', '-0.8745', '-0.515', '0.01008', '0.2025', '-0.1245', '0.2712', '0.3887', '0.2961', '-0.3796', '0.331', '-0.2559', '-0.06204', '0.2003', '0.2366', '0.314', '0.555', '-0.336', '-0.04507', '-0.6514', '-0.01595', '-0.8584', '-0.1918', '-0.7705', '-0.129', '-0.0535', '-0.2395', '-0.1198', '-0.1594', '0.6084', '0.10724', '0.3303', '0.5034', '-0.06192', '-0.0346', '0.05518', '-0.346', '-0.8857', '-0.03006', '-0.5483', '0.0249', '0.10944', '0.4075', '0.02864', '-0.287', '-0.1315', '-0.1073', '-0.2292', '0.2554', '0.468', '-0.1399', '0.0618', '-0.384', '0.0476', '0.4897', '-0.685', '0.05994', '0.2888', '-0.2732', '0.2102', '-0.2185', '0.03586', '0.1975', '0.1294', '-0.1897', '0.1638', '-0.0792', '0.1334', '-0.482', '0.0764', '0.4832', '-0.01239', '-0.5396', '0.011444', '0.11176', '0.605', '0.839', '0.2074', '0.7046', '-0.547', '0.224', '-0.0824']",,,,,,,
mondo:0011019,alopecia-intellectual disability-hypergonadotropic hypogonadism syndrome,"['alopecia-mental retardation syndrome with convulsions and hypergonadotropic hypogonadism', 'Devriendt-Vandenberghe-Fryns syndrome', 'alopecia-intellectual disability syndrome with convulsions and hypergonadotropic hypogonadism']",,601217,1014,,,,,C563370,,,,
mondo:0011020,osteoporosis-oculocutaneous hypopigmentation syndrome,"['osteoporosis oculocutaneous hypopigmentation syndrome', 'osteoporosis and oculocutaneous hypopigmentation syndrome', 'OOCHS', 'OOCH syndrome', 'Hernández-Fragoso syndrome', 'OOCH']",,601220,2786,C1832592,,,,C536062,,,,
mondo:0011021,"neuronal intestinal dysplasia, type B","['NID B', 'neuronal intestinal dysplasia, type B']",0080680,601223,,C1832589,,,,,,,,
mondo:0011022,Potocki-Shaffer syndrome,"['11p11.2 deletion', 'PSS', 'Potocki-Shaffer syndrome', 'proximal 11P deletion syndrome', 'proximal 11p deletion syndrome', 'Defect11 syndrome', 'deletion of chromosome 11p11.2', 'chromosome 11P11.2 deletion syndrome']",0111687,601224,52022,C1832588,"['-0.374', '-0.1009', '0.5215', '-0.3577', '0.10425', '-0.5933', '-0.01619', '0.4133', '-0.6763', '-0.1771', '0.083', '0.07623', '0.3184', '-0.3916', '-0.2375', '0.02153', '0.03253', '-0.2817', '-0.0835', '-0.1388', '0.0816', '0.1771', '-0.02016', '-0.405', '0.856', '-0.08307', '-0.4485', '0.07764', '0.3733', '-0.1047', '0.4417', '-0.2303', '0.2676', '0.01907', '0.0701', '-0.382', '-0.2146', '-0.392', '-0.0757', '-0.4104', '0.4934', '0.004623', '0.1927', '-0.283', '0.1555', '-0.5083', '0.01444', '0.1282', '-0.2208', '-0.1311', '-0.3635', '0.019', '-0.561', '0.3894', '-0.2177', '-0.5063', '0.0759', '-0.1447', '-0.3525', '0.4253', '0.02782', '-0.01689', '-0.508', '0.1263', '-0.3804', '0.2542', '0.03403', '0.376', '-0.521', '0.2339', '-0.3757', '0.317', '0.05692', '-0.1279', '-0.3857', '0.3237', '0.3418', '-0.1636', '-0.3044', '0.12244', '0.1929', '0.1561', '0.03976', '0.8027', '0.0708', '-0.02016', '-0.2842', '0.6455', '0.04572', '0.4219', '-0.3235', '0.657', '0.2783', '-0.06094', '1.266', '-0.1743', '0.4092', '-0.3196', '0.8496', '0.1837']",C75456,,C538356,758.39,,,
mondo:0011023,hereditary mixed polyposis syndrome,['HMPS'],0111684,,157794,CN240759,"['0.2915', '0.1028', '-0.2184', '-0.1698', '0.00721', '-0.3228', '-0.06116', '0.1974', '-0.0359', '0.1715', '0.1106', '0.0894', '-0.003199', '-0.2642', '-0.0465', '-0.3252', '-0.0826', '0.02097', '0.1067', '-0.419', '0.02786', '-0.112', '0.2357', '-0.1826', '0.2998', '0.1641', '0.03583', '-0.0404', '0.0679', '-0.1987', '0.1857', '-0.1091', '0.1106', '0.1321', '0.0846', '0.01889', '-0.283', '-0.2207', '0.01573', '-0.1774', '0.1181', '-0.432', '0.0704', '-0.1982', '0.1593', '-0.0875', '-0.1952', '0.1974', '0.1499', '0.1375', '0.0298', '0.1499', '-0.1873', '-0.2708', '-0.2443', '-0.2361', '-0.0308', '-0.05356', '-0.4868', '-0.08704', '0.509', '0.06836', '0.2423', '0.0469', '0.07324', '0.265', '0.3955', '0.2087', '-0.33', '0.4324', '-0.0572', '-0.1198', '0.06635', '-0.1935', '0.03516', '-0.0746', '-0.217', '0.1271', '-0.1339', '-0.185', '-0.03333', '0.1648', '-0.1326', '0.2058', '-0.2893', '-0.358', '0.099', '0.07623', '-0.03778', '-0.1849', '0.07446', '0.06107', '0.1115', '-0.02103', '0.362', '0.11615', '0.4595', '-0.3298', '-0.458', '0.136']",,,C563365,,,,
mondo:0011024,"dermatitis herpetiformis, familial","['DH', 'Duhring Brocq disease', 'hereditary dermatitis herpetiformis', 'Brocq-Duhring disease', 'Duhring^s disease', 'dermatitis herpetiformis, familial']",,601230,,C1832586,,,,C538218,,,,
mondo:0011025,Cayman type cerebellar ataxia,"['cerebellar ataxia, Cayman type', 'ataxia, cerebellar, Cayman type', 'ATCAY', 'Cayman ataxia', 'cerebellar ataxia, CAYMAN type', 'Cayman cerebellar ataxia']",0060694,601238,94122,C1832585,"['-0.245', '-0.3682', '0.0986', '0.05945', '-0.1145', '-0.9355', '0.2937', '0.1288', '-0.6685', '-1.043', '0.2126', '0.3384', '-0.1774', '0.06433', '0.4534', '-0.3652', '-0.1015', '-0.2935', '0.0196', '-1.012', '-0.011055', '-0.2651', '0.1404', '-0.705', '0.5186', '-0.43', '-0.3442', '-0.0565', '-0.03345', '-0.691', '0.1761', '0.3315', '-0.5938', '-0.3276', '0.461', '0.147', '-0.1648', '0.1685', '0.504', '0.3918', '0.2231', '0.2429', '-0.4958', '0.2927', '0.551', '-0.621', '0.1425', '0.4177', '0.3103', '-0.1443', '-0.2683', '0.0868', '-0.09216', '-0.5415', '-0.1094', '-0.781', '0.3894', '0.4644', '-0.2053', '0.5537', '-0.569', '0.3557', '0.2115', '-0.1869', '-0.455', '0.6104', '0.2231', '0.4426', '-0.727', '0.5386', '0.871', '0.646', '-0.1284', '-0.79', '0.437', '0.5337', '0.4443', '0.276', '0.1742', '0.5166', '-0.2668', '-0.639', '0.3018', '0.777', '-0.3274', '-0.574', '0.2866', '0.0858', '0.4253', '0.4966', '0.3706', '0.46', '0.2343', '0.0783', '1.017', '0.9604', '0.3962', '0.6016', '-0.205', '-0.01488']",,,C563363,,,,
mondo:0011026,autosomal recessive congenital ichthyosis 4A,"['ICR2B', 'ichthyosis congenita 2B', 'ichthyosis, lamellar, 2, formerly', 'lamellar ichthyosis, type 2', 'ARCI4A', 'ichthyosis, congenital, autosomal recessive 4A', 'ichthyosis lamellar 2', 'autosomal recessive congenital ichthyosis type 4A', 'ichthyosis congenita IIB', 'ichthyosis, congenital, autosomal recessive type 4A', 'lamellar ichthyosis 2', 'ichthyosis, lamellar, 2', 'LI2']",0060712,601277,,,"['-0.02553', '0.0487', '-0.002316', '-0.019', '0.03023', '-0.04913', '0.000885', '0.03677', '-0.03061', '-0.03705', '-0.006428', '0.001201', '-0.009895', '0.00657', '-0.01435', '-0.01617', '0.002937', '-0.0207', '-0.02232', '-0.08606', '-0.01688', '-0.011765', '0.04062', '-0.015114', '0.02023', '0.001771', '-0.02127', '-0.014885', '0.01614', '-0.04636', '0.03854', '-0.00455', '0.04556', '0.02478', '0.00683', '-0.02116', '-0.00959', '-0.0289', '-0.006958', '-0.0533', '0.01752', '-0.0598', '0.02948', '0.00792', '-0.013145', '-0.04282', '-0.007904', '0.0349', '0.0171', '0.02109', '0.004467', '-0.01142', '0.004166', '-0.01421', '-0.02705', '-0.02986', '0.05295', '0.00986', '-0.05228', '-0.002516', '0.03256', '0.01099', '0.003063', '0.0095', '0.01063', '0.0004401', '0.0589', '0.04333', '-0.04175', '0.0474', '-0.0526', '-0.004116', '0.01727', '-0.03162', '0.01938', '0.02289', '-0.001771', '-0.0121', '-0.01892', '-0.02034', '-0.0008874', '-0.01775', '0.001215', '0.0523', '0.006527', '0.01088', '0.0154', '0.0437', '0.04517', '0.03061', '0.01564', '0.05057', '0.004257', '0.01735', '0.09485', '0.03513', '0.0462', '-0.05594', '0.004055', '0.003714']",,,C537264,,,,
mondo:0011027,"diabetes mellitus, noninsulin-dependent, 1","['noninsulin-dependent diabetes mellitus 1', 'diabetes mellitus, noninsulin-dependent 1', 'NIDDM1', 'diabetes mellitus, noninsulin-dependent, 1', 'diabetes mellitus, noninsulin-dependent, type 1']",,601283,,C1832544,,,,C563359,,,,
mondo:0011028,autosomal recessive limb-girdle muscular dystrophy type 2F,"['autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCD', 'muscular dystrophy, limb-girdle, type 2F', 'limb-girdle muscular dystrophy type 2F', 'muscular dystrophy limb-girdle with delta-sarcoglyan deficiency', 'delta-sarcoglycanopathy', 'SGCD autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, limb-girdle, autosomal recessive 6', 'limb-girdle muscular dystrophy due to delta-sarcoglycan deficiency', 'LGMD2F']",0110280,601287,219,,"['-0.1687', '-0.7407', '-0.5806', '-0.4727', '0.6743', '-1.066', '0.2595', '0.807', '-1.833', '-0.903', '-0.138', '0.475', '-0.468', '0.65', '0.1198', '0.3804', '-0.8193', '-0.4585', '-0.7207', '-0.8647', '0.2336', '0.002743', '0.2026', '0.7007', '0.3877', '0.2361', '-0.05634', '-1.171', '0.3027', '-0.754', '0.6694', '0.1251', '0.582', '0.2615', '-0.01695', '-0.04132', '-0.5386', '0.517', '0.2267', '-0.4177', '0.023', '-0.563', '-0.3047', '0.4124', '-0.5015', '-0.06207', '0.1785', '0.3992', '-0.1737', '0.8237', '0.4146', '-0.3728', '0.2998', '-1.0625', '0.2695', '-0.7817', '0.3687', '0.805', '-0.2062', '-0.0557', '0.2374', '0.1375', '0.0433', '-0.2325', '-0.2346', '-0.0875', '-0.02092', '0.691', '-0.571', '-0.3623', '-0.1748', '0.4326', '0.2279', '0.1974', '0.753', '0.5776', '-0.2025', '0.3333', '0.051', '-0.1337', '0.2333', '0.3718', '0.1881', '-0.3445', '-0.3704', '0.4897', '-0.153', '-0.2327', '0.837', '0.327', '-0.08417', '-0.01884', '0.43', '0.8823', '-0.0641', '0.1443', '0.658', '-0.57', '-0.55', '-0.2386']",,,C535896,,,,
mondo:0011029,myeloid tumor suppressor,"['myeloid tumor suppressor', 'myeloid leukemia-related locus']",,601308,,,,,,,,,,
mondo:0011030,"epithelial basolateral chloride conductance regulator, rabbit, homolog of","['Ebcr', 'epithelial basolateral chloride conductance regulator, rabbit, homolog of']",,601315,,,,,,,,,,
mondo:0011031,autosomal dominant nonsyndromic hearing loss 10,"['DFNA10', 'autosomal dominant nonsyndromic deafness type 10', 'autosomal dominant deafness 10', 'deafness, autosomal dominant 10', 'autosomal dominant nonsyndromic deafness 10', 'EYA4 autosomal dominant nonsyndromic deafness', 'deafness, autosomal dominant type 10', 'autosomal dominant nonsyndromic deafness caused by mutation in EYA4']",0110542,601316,,C1832476,,,,C563354,,,,
mondo:0011032,autosomal dominant nonsyndromic hearing loss 11,"['autosomal dominant deafness 11', 'autosomal dominant nonsyndromic deafness type 11', 'deafness, autosomal dominant 11', 'autosomal dominant nonsyndromic deafness 11', 'MYO7A autosomal dominant nonsyndromic deafness', 'deafness, autosomal dominant type 11', 'autosomal dominant nonsyndromic deafness caused by mutation in MYO7A', 'DFNA11']",0110543,601317,,C1832475,,,,C563353,,,,
mondo:0011033,type 1 diabetes mellitus 13,"['IDDM13', 'insulin-dependent diabetes mellitus 13', 'diabetes mellitus, insulin-dependent, 13']",0110752,601318,,C1832474,,,,C563352,,,,
mondo:0011034,odontomicronychial dysplasia,"['odonto-micronychial dysplasia', 'ectodermal dysplasia, nail/Tooth type', 'odontomicronychial dysplasia']",,601319,1811,C1832473,,,,C537741,,,,
mondo:0011035,neurofibromatosis-Noonan syndrome,"['NFNS', 'neurofibromatosis with Noonan phenotype', 'neurofibromatosis type 1-Noonan syndrome', 'Noonan-neurofibromatosis syndrome', 'Noonan neurofibromatosis syndrome', 'neurofibromatosis-Noonan syndrome']",0111683,601321,638,,"['0.06396', '-0.0891', '0.732', '-0.3594', '-0.07117', '0.1182', '-0.162', '0.876', '-0.628', '-0.799', '0.517', '-0.126', '0.0944', '0.26', '-0.415', '0.1066', '-0.6025', '-0.3945', '-0.505', '-0.047', '-0.2471', '0.11066', '0.11096', '-0.4902', '0.2341', '-0.05023', '-0.5894', '0.364', '1.432', '0.3342', '1.0205', '-0.7104', '0.2761', '0.627', '-0.3655', '-0.4573', '-0.37', '0.7397', '0.2', '-0.829', '0.8853', '0.7124', '-0.005775', '-0.319', '0.03406', '-0.3508', '0.06573', '0.3337', '0.5547', '-0.354', '-0.2279', '0.1877', '-0.3708', '0.2642', '-0.156', '-0.545', '-0.1013', '0.3828', '-0.085', '-0.276', '0.2502', '-0.4443', '0.3225', '-0.141', '0.2634', '-0.002335', '-0.174', '0.3406', '-0.1691', '0.8647', '0.397', '0.348', '0.2102', '0.1444', '0.5605', '0.1411', '0.4172', '0.3162', '-0.2727', '-0.6543', '0.503', '-0.1078', '-0.0994', '-0.0878', '-0.373', '-0.5312', '0.7373', '-0.1293', '1.004', '0.663', '-0.0341', '0.5835', '-0.0642', '-0.4797', '0.7246', '-0.4375', '0.294', '-0.1874', '0.185', '0.2854']",,,D009456,,,,
mondo:0011036,porencephaly-cerebellar hypoplasia-internal malformations syndrome,"['Bonnemann Meinecke syndrome', 'porencephaly cerebellar hypoplasia internal malformations', 'porencephaly, cerebellar hypoplasia, and internal malformations', 'Bonnemann-Meinecke syndrome']",,601322,2941,C1832472,,,,C536336,,,,
mondo:0011037,"renal dysplasia, cystic, susceptibility to","['CYSRD', 'renal dysplasia, cystic, susceptibility to', 'renal dysplasia diffuse cystic', 'diffuse cystic renal dysplasia']",0111682,601331,,,,,,C537755,,,,
mondo:0011038,cerebellar ataxia-areflexia-pes cavus-optic atrophy-sensorineural hearing loss syndrome,"['CAPOS', 'cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss', 'cerebellar ataxia - areflexia - pes cavus - optic atrophy - sensorineural hearing loss', 'cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss', 'CAPOS syndrome']",,601338,1171,,"['0.5703', '0.2357', '0.1589', '0.7793', '-0.5645', '-0.06256', '0.941', '0.7666', '-0.4785', '-0.83', '0.2817', '0.05737', '-0.7915', '0.0539', '-0.305', '-0.806', '-0.4907', '0.00867', '-0.3164', '-0.2917', '-0.1133', '0.1971', '-0.864', '0.2979', '0.6963', '0.4277', '-0.842', '0.006767', '-0.6343', '-0.3367', '-0.12134', '0.1797', '0.2673', '-0.2263', '-0.5', '-0.217', '-0.3816', '-0.5347', '-0.2153', '-0.9272', '0.01628', '-0.3208', '-0.309', '-0.1078', '0.1641', '-1.16', '0.02853', '0.587', '0.10657', '-0.542', '-0.0591', '-0.4016', '-0.3833', '-0.2874', '0.559', '0.5273', '0.1455', '-0.0895', '-0.3691', '0.478', '0.0748', '0.942', '-0.3757', '0.4038', '-0.9434', '0.2825', '-0.4175', '0.9717', '-0.0965', '-0.2495', '0.2178', '0.714', '1.053', '-1.125', '0.6885', '-0.1672', '0.8926', '0.588', '0.4917', '-0.03503', '0.04608', '-0.7324', '-0.4102', '0.833', '0.1903', '-0.238', '0.01047', '1.154', '-0.1339', '0.914', '-0.03543', '0.3625', '-0.10815', '0.5186', '0.4067', '0.1213', '0.2788', '-0.768', '-0.04187', '0.08527']",,,C535351,,,,
mondo:0011039,"atrophia maculosa varioliformis cutis, familial","['varioliform macular atrophy of the skin', 'atrophia maculosa varioliformis cutis, familial', 'AMVC', 'atrophia MACULOSA VARIOLIFORMIS cutis, familial']",,601341,,C1832465,,,,C563349,,,,
mondo:0011040,"spinal dysplasia, Anhalt type","['spinal dysplasia, Anhalt type']",,601344,,C1832464,,,,C563348,,,,
mondo:0011041,"ectodermal dysplasia with natal teeth, Turnpenny type","['ectodermal dysplasia with natal teeth, Turnpenny type', 'ectodermal dysplasia, hair/Tooth type', 'ectodermal dysplasia with natal teeth Turnpenny type']",,601345,69083,C1832444,,,,C563347,,,,
mondo:0011042,Martinez-Frias syndrome,"['pancreatic hypoplasia, intestinal atresia, and gallbladder aplasia or hypoplasia, with or without tracheoesophageal fistula', 'Martínez-Frías syndrome', 'Martinez-Frias syndrome']",,601346,137862,CN199270,,,,C563346,,,,
mondo:0011043,"myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay","['myelodysplasia, immunodeficiency, facial dysmorphism, short stature, and psychomotor delay']",,601347,,C1832442,,,,C563345,,,,
mondo:0011044,"ectrodactyly of lower limbs, congenital heart defect, and micrognathia","['ectrodactyly of lower limbs, congenital heart defect, and micrognathia']",,601348,,C1832441,,,,C563344,,,,
mondo:0011045,MMEP syndrome,"['MCOPS8', 'MMEP', 'microphthalmia, syndromic 8', 'microphthalmia syndromic 8', 'Viljoen Smart syndrome', 'microcephaly microphthalmia ectrodactyly of lower limbs and prognathism', 'microcephaly, microphthalmia, ectrodactyly of Lower limbs, and prognathism', 'microcephaly-microphthalmia-ectrodactyly of lower limbs-prognathism syndrome', 'syndromic microphthalmia type 8', 'Viljoen-Smart syndrome']",0111803,601349,3434,C4275099,,,,C537686,,,,
mondo:0011046,"short stature, Brussels type","['short stature syndrome, Brussels type', 'Mievis-Verellen-Dumoulin syndrome', 'familial short stature with facial dysmorphism and osteochondrodysplastic lesions', 'Mievis Verellen-Dumoulin syndrome']",,601350,2867,C1832439,,,,C537121,,,,
mondo:0011047,deafness-epiphyseal dysplasia-short stature syndrome,"['deafness, femoral epiphyseal dysplasia, short stature and developmental delay', 'chitty-Hall-Baraitser syndrome', 'growth retardation, deafness, femoral epiphyseal dysplasia, and lacrimal duct obstruction', 'deafness, epiphyseal dysplasia, short stature']",,601351,3218,C1832438,,,,C535928,,,,
mondo:0011048,epilepsy-microcephaly-skeletal dysplasia syndrome,"['Battaglia-Neri syndrome', 'epilepsy - microcephaly - skeletal dysplasia', 'intellectual disability, microcephaly, epilepsy, and coarse face', 'mental retardation, microcephaly, epilepsy, and coarse face']",,601352,1948,,,,,,,,,
mondo:0011049,Fine-Lubinsky syndrome,"['brachycephaly, deafness, cataract and mental retardation', 'brachycephaly, deafness, cataract, microstomia, and intellectual disability', 'brachycephaly, deafness, cataract and intellectual disability', 'brachycephaly, deafness, cataract, microstomia, and mental retardation', 'brachycephaly-deafness-cataract-intellectual disability syndrome', 'fine-Lubinsky syndrome']",,601353,1272,C0795941,,,,C537933,,,,
mondo:0011050,microcephaly-cardiac defect-lung malsegmentation syndrome,"['microcephaly, congenital heart disease, lung segmentation defects and unilateral renal agenesis', 'microcephaly, congenital heart disease, unilateral renal agenesis, and hyposegmented lungs', 'Ellis-Yale-Winter syndrome', 'Ellis Yale Winter syndrome']",,601355,2516,,,,,C563341,,,,
mondo:0011051,"lethal short-limb skeletal dysplasia, Al Gazali type","['lethal neonatal short limb dwarfism', 'dysplastic cortical hyperostosis, Al-Gazali type', 'lethal short-limb skeletal dysplasia, Al Gazali type', 'lethal short limb skeletal dysplasia Al Gazali type']",,601356,646136,C1832435,,,,C537598,,,,
mondo:0011052,amelia cleft lip palate hydrocephalus iris coloboma,"['brachial amelia, forebrain defects and facial clefts', 'ACLH', 'brachial AMELIA, cleft LIP, and holoprosencephaly', 'bilateral brachial amelia, facial clefts, encephalocele, orbital cyst and omphalocele', 'brachial amelia, forebrain defects, and Facial clefts', 'amelia cleft lip palate hydrocephalus iris coloboma']",,601357,,C1832434,,,,C536713,,,,
mondo:0011053,intellectual disability-sparse hair-brachydactyly syndrome,"['Nicolaides-Baraitser syndrome', 'NCBRS', 'SMARCA2-related BAFopathy', 'NBs', 'sparse hair and intellectual disability', 'sparse hair and mental retardation', 'NICOLAIDES-Baraitser syndrome']",,601358,3051,C1303073,"['0.3608', '0.3706', '-0.0342', '-0.0335', '-0.4124', '-0.3599', '0.566', '1.105', '-0.846', '-0.695', '-0.416', '0.0798', '0.2632', '0.03513', '0.1871', '-0.00988', '0.9033', '0.02643', '-0.05225', '-0.9517', '-0.3347', '0.02632', '0.1763', '-0.2432', '0.3489', '0.01576', '-0.371', '0.5586', '0.1036', '-0.1661', '0.7007', '-0.725', '-0.4585', '0.564', '0.16', '0.3333', '-0.2783', '-0.0645', '-0.1887', '-0.2279', '0.2457', '-0.01001', '-0.2031', '0.1414', '0.1633', '0.00631', '0.03021', '0.2397', '-0.2788', '-0.4006', '-0.3992', '0.1362', '-0.1976', '-0.0699', '-0.2756', '0.1411', '-0.203', '-0.2715', '0.1124', '-0.05048', '0.10767', '0.0516', '0.0452', '0.549', '-0.456', '0.05133', '-0.0656', '-0.01631', '-0.5786', '0.1614', '0.1123', '0.03625', '-0.304', '0.1824', '0.2976', '0.663', '0.4473', '-0.8594', '-0.749', '-0.2467', '0.37', '0.02768', '-0.4475', '0.1732', '0.3274', '0.4602', '-0.5728', '0.2224', '0.2532', '0.3813', '0.3281', '-0.02687', '-0.501', '0.577', '0.2578', '-0.2617', '0.262', '-0.833', '0.4524', '0.3247']",,,C536116,,,,
mondo:0011054,autosomal recessive amelia,"['amelia, autosomal recessive', 'Amelia, posterior, with pelvic and pulmonary hypoplasia syndrome']",,601360,1027,C1832432,"['-0.3203', '0.3186', '0.0793', '-0.519', '-0.0942', '-0.279', '-0.3066', '0.675', '-0.4712', '-0.3247', '-0.04492', '-0.401', '0.2903', '0.0228', '-0.2474', '0.141', '0.52', '0.2673', '-0.713', '-0.1268', '-0.1444', '-0.0862', '0.7417', '-0.5317', '0.1687', '-0.0593', '-0.3865', '0.2524', '0.7637', '-0.7715', '0.3833', '-0.1714', '-0.02881', '0.03964', '0.02043', '0.02187', '-0.0223', '-0.323', '-0.08746', '-0.425', '-0.003244', '-0.6323', '-0.579', '-0.2408', '0.0544', '-0.2275', '-0.2198', '0.1255', '-0.3113', '0.06885', '-0.4182', '-0.2744', '-0.2114', '0.294', '-0.4656', '-0.784', '0.07324', '0.1663', '0.0853', '0.126', '-0.202', '-0.1663', '-0.05472', '0.4731', '-0.2544', '-0.205', '0.2084', '0.3508', '-0.4512', '0.7554', '-0.2227', '0.6323', '0.1738', '0.0904', '-0.223', '0.3433', '-0.0262', '-0.2673', '-0.11365', '-0.03564', '0.013054', '0.04672', '0.9116', '0.481', '0.000582', '0.2852', '0.05746', '0.7656', '0.1459', '0.0647', '-0.2444', '0.3523', '0.2656', '0.06744', '0.8857', '0.1647', '0.317', '-0.847', '-0.09283', '-0.1677']",,,C563338,,,,
mondo:0011055,distal monosomy 10p,"['DiGeorge syndrome/velocardiofacial syndrome Complex type 2', '10p monosomy', '10p13-p14 Deletion syndrome', 'chromosome 10p deletion', 'partial monosomy 10p', 'distal monosomy type 10p', 'DiGeorge syndrome/velocardiofacial syndrome complex 2', 'DiGeorge syndrome/velocardiofacial syndrome complex-2', 'deletion 10p', '10p deletion', 'monosomy 10p', 'DiGeorge syndrome type 2', 'Dgs2', 'telomeric deletion 10p', 'distal 10p deletion', 'monosomy 10pter']",,601362,1580,C4304502,,C130982,,C563337,,,,
mondo:0011056,Wilms tumor 4,"['Wilms tumor, type 4', 'familial Wilms tumour 1', 'Wilms tumor type 4', 'Wilms tumor 4', 'Wilms tumour type 4', 'WT4', 'familial Wilms tumor 1']",,601363,,C1832426,,,,C563336,,,,
mondo:0011057,cerebrovascular disorder,"['stroke', 'cerebrovascular disease', 'cerebrovascular accident', 'cerebrovascular disorder', 'CVA', 'CVA (cerebral vascular accident)', 'cerebral infarction']",6713,,,C0007820,,C2938,0003763,D002561,437.9,I60-I69,,
mondo:0011058,autosomal dominant nonsyndromic hearing loss 9,"['autosomal dominant nonsyndromic deafness type 9', 'autosomal dominant nonsyndromic deafness caused by mutation in COCH', 'autosomal dominant nonsyndromic deafness 9', 'deafness, autosomal dominant 9', 'autosomal dominant deafness 9', 'COCH autosomal dominant nonsyndromic deafness', 'deafness, autosomal dominant type 9', 'DFNA9']",0110593,601369,,C1832425,,,,C563335,,,,
mondo:0011059,holoprosencephaly-craniosynostosis syndrome,"['Genoa syndrome', 'holoprosencephaly craniosynostosis', 'Camero-Lituania-Cohen syndrome', 'holoprosencephaly, SEMILOBAR, with craniosynostosis', 'Semilobar holoprosencephaly and primary craniosynostosis', 'camera Lituania Cohen syndrome']",,601370,2163,C1832424,,,,C537684,,Q04.2,,
mondo:0011060,early-onset non-syndromic cataract,"['nuclear sclerosis of the lens', 'cataract, age-related nuclear']",,601371,91492,C1832423,,,,,,,,
mondo:0011061,"chorea, remitting, with nystagmus and cataract","['familial remitting chorea, nystagmus and cataracts', 'chorea, remitting, with nystagmus and cataract', 'chorea, remitting with nystagmus and cataracts']",,601372,,C1832422,,,,C535355,,,,
mondo:0011062,aprosencephaly cerebellar dysgenesis,['aprosencephaly and cerebellar dysgenesis'],,601374,1126,C1832412,,,,C563331,,,,
mondo:0011063,"hidrotic ectodermal dysplasia, Christianson-Fourie type","['Christianson-Fourie syndrome', 'ectodermal dysplasia, hidrotic, Christianson-Fourie type']",,601375,1808,C1832411,,,,C536180,,,,
mondo:0011064,"lethal chondrodysplasia, Seller type","['chondrodysplasia, lethal, with long bone angulation and mixed bone density', 'lethal chondrodysplasia seller type']",,601376,1421,C1832410,,,,C563330,,,,
mondo:0011065,Hunter-McAlpine craniosynostosis,"['Hunter-McAlpine syndrome', 'craniosynostosis, mental deficiency, almond-shaped palpebral fissures, downturned mouth, mild acral-skeletal anomalies, and short stature', 'Hunter-McAlpine craniosynostosis syndrome']",,601379,97340,C1832408,,,,C536072,,,,
mondo:0011066,Charcot-Marie-Tooth disease type 4B1,"['CMT 4B1', 'MTMR2 Charcot-Marie-Tooth disease type 4', 'Charcot-Marie-Tooth disease, autosomal recessive, with focally folded myelin sheaths, autosomal recessive, type 4B1', 'CMT 4B', 'Charcot-Marie-Tooth disease, type 4B', 'Charcot-Marie-Tooth neuropathy, type 4B1', 'Charcot-Marie-Tooth disease, type 4B1', 'Charcot Marie Tooth disease type 4B1', 'Charcot-Marie-Tooth disease type 4 caused by mutation in MTMR2', 'CMT4B1', 'Charcot-Marie-Tooth neuropathy type 4B1', 'autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B1']",0110191,601382,99955,C1832399,"['0.12274', '0.3552', '-0.04303', '-0.2422', '-0.2722', '-0.12463', '-0.1136', '0.8374', '-0.652', '-0.3235', '-0.01926', '0.4138', '-0.5703', '0.6245', '-0.27', '0.0773', '-0.1737', '-0.514', '-0.601', '-0.2142', '0.3599', '0.0768', '0.2693', '0.6553', '0.05365', '0.51', '0.003378', '0.1763', '0.3699', '-0.2383', '0.12164', '-0.6045', '0.0983', '-0.1946', '0.0912', '-0.888', '-0.2277', '-0.252', '0.7056', '-0.1339', '-1.526', '-0.5664', '-0.492', '0.0271', '-0.1869', '-0.302', '-0.07275', '-0.3198', '-0.3455', '-0.2067', '-0.1316', '0.2002', '-0.2742', '-1.106', '0.5244', '-0.3462', '0.2113', '0.1317', '-0.334', '0.03705', '-0.3018', '-0.1432', '0.35', '0.477', '-0.7393', '1.067', '0.0841', '0.6787', '-0.673', '0.354', '-0.7837', '0.2319', '0.3384', '0.2817', '1.101', '0.623', '-0.4902', '0.559', '0.11127', '-0.4016', '0.238', '-0.01685', '0.985', '0.8687', '-0.0592', '-0.0431', '0.3855', '0.886', '0.665', '0.3232', '0.2177', '-0.04272', '-0.06024', '0.2505', '0.671', '0.374', '0.5977', '-0.398', '-0.08154', '0.2966']",,,C535420,,,,
mondo:0011067,autosomal recessive nonsyndromic hearing loss 12,"['autosomal recessive deafness 12', 'DFNB12', 'autosomal recessive nonsyndromic deafness type 12', 'deafness, autosomal recessive 12', 'autosomal recessive nonsyndromic deafness 12', 'deafness, autosomal recessive 12, modifier of', 'deafness, autosomal recessive type 12']",0110467,601386,,C1832394,,,,C563327,,,,
mondo:0011068,type 1 diabetes mellitus 12,"['CTLA4 type 1 diabetes mellitus', 'type 1 diabetes mellitus caused by mutation in CTLA4', 'diabetes mellitus, insulin-dependent, 12', 'insulin-dependent diabetes mellitus 12', 'diabetes mellitus, insulin-dependent, type 12', 'IDDM12']",0110751,601388,,C1832392,,,,C563326,,,,
mondo:0011069,"cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction","['cervical ribs, Sprengel anomaly, preaxial polydactyly, anal atresia, and urethral obstruction', 'cervical ribs, Sprengel anomaly, anal atresia, and urethral obstruction', 'Frydman Cohen Ashkenazi syndrome']",,601389,,C1832391,,,,C538072,,,,
mondo:0011070,van Maldergem syndrome 1,"['VAN Maldergem syndrome 1', 'VMLDS1', 'van Maldergem syndrome caused by mutation in DCHS1', 'DCHS1 van Maldergem syndrome', 'van Maldergem syndrome 1', 'Van Maldergem syndrome type 1', 'Cerebrofacioarticular syndrome']",0080585,601390,,,,,,,,,,
mondo:0011071,hereditary thrombocytopenia and hematologic cancer predisposition syndrome,"['familial platelet syndrome with predisposition to acute myelogenous leukaemia', 'thrombocytopenia, familial, with propensity to acute myelogenous leukaemia', 'familial thrombocytopenia with propensity to acute myelogenous leukaemia']",,,71290,C1832388,"['0.1967', '0.03793', '0.1514', '0.4104', '0.6733', '-0.5127', '0.3792', '0.5728', '0.0786', '-0.3196', '0.687', '0.0537', '-0.2363', '0.1366', '-0.0833', '-0.3708', '-0.2734', '-0.458', '-0.602', '-0.434', '0.051', '-0.5513', '-0.3857', '-0.02246', '0.4104', '-0.637', '0.3674', '0.303', '0.376', '0.005356', '0.3547', '-0.3926', '0.5024', '-0.537', '0.678', '-0.3533', '-0.982', '0.04306', '-0.2032', '-0.1251', '0.3042', '0.09357', '0.1444', '-0.258', '-0.141', '-0.01712', '-0.416', '-0.881', '1.398', '-0.2035', '0.00763', '-0.595', '0.2815', '-0.2373', '-0.1368', '0.3374', '-0.468', '0.05667', '-1.014', '-1.143', '0.4292', '0.007122', '-0.08', '-0.508', '-0.152', '0.6016', '0.08276', '0.1355', '0.2454', '0.8843', '-0.0406', '0.78', '-0.03232', '-0.04788', '1.316', '0.382', '0.2954', '0.0788', '-0.07324', '0.2888', '-0.3499', '0.2089', '0.08435', '-0.154', '-0.27', '0.1823', '1.034', '0.3787', '0.641', '-0.5903', '0.0891', '-6.616e-05', '-0.326', '0.2021', '0.1236', '0.393', '-0.00822', '-0.8306', '-0.5312', '-0.1755']",,,C563324,,,,
mondo:0011072,"diabetes mellitus, noninsulin-dependent, 2","['noninsulin-dependent diabetes mellitus 2', 'diabetes mellitus, noninsulin-dependent, 2', 'NIDDM2']",,601407,,C1832387,,,,C563323,,,,
mondo:0011073,"diabetes mellitus, transient neonatal, 1","['Dmtn', 'diabetes mellitus, transient neonatal, type 1', 'diabetes mellitus, transient neonatal 1', 'Tndm1', 'diabetes mellitus, transient neonatal, 1', 'Tndm']",,601410,99886,,"['0.7017', '-0.0109', '0.06012', '0.8813', '-0.53', '-0.822', '-0.1968', '0.978', '0.02238', '-0.6616', '-0.418', '-0.3086', '0.3264', '0.2966', '-0.993', '-0.2386', '0.1802', '-0.1309', '0.004356', '-0.745', '0.0945', '-0.1401', '0.1459', '0.093', '-0.67', '-0.235', '0.02344', '0.1594', '0.6167', '-0.359', '0.619', '-0.213', '0.1032', '-0.06052', '-0.1526', '0.4849', '-0.5635', '0.5806', '-0.2095', '0.11523', '0.0447', '0.4846', '0.1848', '0.3865', '-0.2257', '-0.1498', '0.159', '-0.371', '0.02446', '0.08826', '0.000873', '-0.3608', '0.8306', '-0.6245', '0.01735', '0.3516', '-0.1552', '-0.734', '-0.705', '0.79', '-0.521', '0.3494', '-0.02904', '0.3337', '0.05585', '0.507', '-0.4766', '0.4822', '-0.6167', '-0.02757', '0.08606', '0.1992', '0.2437', '0.188', '0.5254', '0.4312', '-0.4617', '0.698', '-0.5015', '-0.01224', '0.4219', '-0.1942', '0.01584', '-0.643', '0.2607', '0.3115', '-0.01967', '0.4253', '0.579', '0.2087', '0.6094', '0.537', '-0.03552', '-0.1409', '0.9697', '0.1059', '-0.009964', '-0.228', '0.2202', '0.37']",,,C563322,,,,
mondo:0011074,autosomal dominant nonsyndromic hearing loss 7,"['autosomal dominant nonsyndromic deafness type 7', 'deafness, autosomal dominant 7', 'autosomal dominant nonsyndromic deafness 7', 'autosomal dominant deafness 7', 'DFNA7']",0110591,601412,,C1832379,,,,C563321,,,,
mondo:0011075,retinitis pigmentosa 18,"['retinitis pigmentosa 18', 'RP18', 'retinitis pigmentosa caused by mutation in PRPF3', 'retinitis pigmentosa type 18', 'PRPF3 retinitis pigmentosa', 'RP 18']",0110356,601414,,C1832378,,,,C563320,,H35.5,,
mondo:0011076,myofibrillar myopathy 1,"['autosomal recessive limb-girdle muscular dystrophy type 2R', 'desminopathy', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in DES', 'CMD1F and LGMD1D, formerly', 'myofibrillar myopathy with arrhythmogenic right ventricular cardiomyopathy', 'desmin-related myopathy with arrhythmogenic right ventricular cardiomyopathy', 'desminopathy, primary', 'inclusion body myopathy 1, autosomal dominant, formerly', 'myofibrillar myopathy type 1', 'IBM1', 'arrhythmogenic right ventricular cardiomyopathy 7', 'DES myofibrillar myopathy (disease)', 'arrhythmogenic right ventricular dysplasia, familial, 7', 'desmin-related myopathy', 'arrhythmogenic right ventricular cardiomyopathy 7, formerly', 'arrhythmogenic right ventricular dysplasia, familial, 7, formerly', 'cardiomyopathy, dilated, 1F and limb-girdle muscular dystrophy type 1D, formerly', 'MFM1', 'myopathy, myofibrillar, 1', 'desmin-related myofibrillar myopathy', 'inclusion body myopathy 1, autosomal dominant', 'cardiomyopathy, dilated, 1F and limb-girdle muscular dystrophy type 1D', 'myopathy, myofibrillar, type 1', 'myopathy, myofibrillar, desmin-related', 'cardiomyopathy, dilated, with conduction defect and muscular dystrophy', 'CMD1F and LGMD1D', 'DES autosomal recessive limb-girdle muscular dystrophy']",0110286,615325,98909,C3809137,"['-0.3787', '0.2927', '-0.02386', '0.4448', '-0.4685', '-0.8677', '0.7856', '0.297', '-0.7886', '-0.2487', '0.02704', '0.2502', '0.502', '0.01746', '0.03058', '-0.1661', '-0.3047', '-0.2905', '-0.663', '-1.33', '0.6343', '0.2454', '0.4065', '0.0839', '0.8906', '-0.2917', '0.1864', '0.2156', '-0.6167', '0.2384', '1.043', '0.545', '0.522', '0.3257', '0.2932', '-0.2966', '0.1415', '0.1698', '0.10297', '-0.5938', '-0.931', '0.2883', '0.2046', '0.773', '-0.679', '0.2625', '-0.07574', '0.0686', '0.1045', '0.1831', '-0.1556', '0.2089', '0.2646', '-0.1317', '0.4521', '-0.694', '0.5933', '0.626', '-0.06122', '-0.1393', '0.3354', '-0.01452', '-0.588', '-0.0921', '-0.883', '0.258', '0.5684', '1.216', '-0.2883', '-0.03568', '-0.2925', '0.4302', '0.3628', '0.4277', '0.199', '-0.2874', '0.4116', '0.26', '-0.4229', '-0.124', '-0.264', '-0.2112', '0.5537', '-0.2915', '-0.07587', '-0.2145', '-0.6455', '0.3455', '0.4487', '0.0793', '0.4006', '-0.4905', '0.06995', '-0.0707', '0.2383', '0.03845', '0.404', '-0.3818', '0.2734', '0.2488']",,,,,,,
mondo:0011077,"microcephaly, corpus callosum dysgenesis, and cleft lip/palate","['microcephaly, facial clefting, and preaxial polydactyly', 'microcephaly, corpus callosum dysgenesis, and cleft lip/palate', 'microcephaly, corpus callosum dysgenesis and cleft lip-palate', 'corpus callosum dysgenesis, microcephaly, infantile spasm, cleft lip-palate, exophthalmos and psychomotor retardation']",,601420,,C1832369,,,,C537547,,,,
mondo:0011078,"anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis","['anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism, and tracheal stenosis', 'Jung Wolff back Stahl syndrome']",,601427,2321,C1832362,,,,C537694,,,,
mondo:0011079,"rhizomelic dysplasia, Patterson-Lowry type","['rhizomelic dysplasia Patterson Lowry type', 'rhizomelic dysplasia, Patterson-Lowry type', 'Patterson Lowry syndrome', 'Patterson-Lowry rhizomelic dysplasia']",,601438,2831,C1832359,,,,C537609,,,,
mondo:0011080,progressive deafness with stapes fixation,"['Thies Reis syndrome', 'Thies-Reis syndrome', 'deafness, progressive, with stapes fixation', 'Stapedo-vestibular ankylosis']",,601449,3235,C1844678,,,,C563316,,,,
mondo:0011081,dislocation of the hip-dysmorphism syndrome,"['hip, congenital dislocation of, with hyperextensibility of fingers and Facial Dysmorphism', 'Collins-Pope syndrome', 'Collins Pope syndrome', 'dislocation of the hip dysmorphism', 'dislocation of hip, congenital, with hyperextensibility of fingers and facial dysmorphism']",,601450,2412,C1832353,,,,C563315,,,,
mondo:0011082,oculoauriculofrontonasal syndrome,"['OCULOAURICULOFRONTONASAL syndrome', 'OAFNS', 'oculoauriculofrontonasal syndrome', 'oculoauriculofrontonasal dysplasia']",,601452,398156,C1832352,,,,C537865,,,,
mondo:0011083,trichodental syndrome,"['Tricho-dental dysplasia', 'TRICHODENTAL dysplasia', 'Tricho-dental syndrome', 'kersey syndrome']",,601453,3351,C0406724,,,,C536551,,,,
mondo:0011084,"psoriasis 3, susceptibility to","['psoriasis susceptibility 3', 'PSORS3', 'psoriasis 3, susceptibility to']",0111283,601454,,,,,,,,,,
mondo:0011085,Charcot-Marie-Tooth disease type 4D,"['Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4D', 'HMSN-Lom', 'HMSN Lom type', 'Charcot-Marie-Tooth disease type 4 caused by mutation in NDRG1', 'Charcot-Marie-Tooth neuropathy type 4D', 'hereditary motor ABD sensory neuropathy Lom type', 'HMSN4D', 'neuropathy, hereditary motor and sensory, Lom type', 'CMT4D', 'hereditary motor and sensory neuropathy, Lom type', 'NMSL', 'HMSN, Lom type', 'autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D', 'Charcot-Marie-Tooth disease, type 4D', 'Charcot-Marie-Tooth neuropathy, type 4D', 'NDRG1 Charcot-Marie-Tooth disease type 4', 'HMSNL']",0110186,601455,99950,C1832334,"['-0.0082', '0.329', '0.1633', '0.2311', '-0.1858', '-0.468', '-0.2688', '0.846', '-0.568', '-0.4573', '-0.01218', '0.3577', '-0.2676', '0.2412', '-0.3694', '-0.4324', '-0.0704', '-0.6035', '-0.545', '-0.1832', '0.3857', '0.03302', '0.11993', '0.5513', '0.2935', '0.5312', '-0.174', '0.3872', '-0.2292', '-0.3232', '0.3462', '-0.297', '-0.2534', '-0.2393', '0.10626', '-0.5605', '-0.1166', '-0.2402', '0.265', '0.1393', '-1.12', '-0.3035', '-0.2474', '0.2196', '-0.2247', '-0.1699', '-0.1456', '-0.3494', '-0.503', '-0.0856', '0.1067', '0.4365', '-0.03186', '-1.032', '0.3027', '-0.2466', '0.1483', '0.2603', '-0.647', '0.24', '-0.5547', '0.2096', '0.2961', '0.6074', '-0.604', '1.074', '0.0503', '0.512', '-0.4258', '0.3406', '-0.669', '0.215', '0.4226', '0.1116', '1.136', '0.7134', '-0.4766', '0.5264', '-0.0777', '-0.08936', '0.0689', '-0.1204', '0.585', '0.902', '-0.0664', '-0.10944', '0.1984', '0.6895', '0.6963', '0.06384', '0.2037', '-0.1809', '0.2783', '0.0053', '0.517', '0.668', '0.5845', '-0.766', '0.07874', '0.5337']",,,C535716,,,,
mondo:0011086,"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive","['severe combined immunodeficiency, B cell-negative', 'severe immunodeficiency, autosomal recessive, T-cell negative, B-cell negative, NK cell-positive', 'SCID, T cell-negative, B cell-negative, NK cell-positive', 'severe combined immunodeficiency due to complete RAG1/2 deficiency', 'SCID, AR, T-cell negative, B-cell negative, NK cell-positive', 'severe combined immunodeficiency due to complete RAG1-2 deficiency', 'SCID due to complete RAG1-2 deficiency', 'SCID due to complete RAG1/2 deficiency', 'severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive']",0090013,601457,331206,C1832322,"['-0.03403', '0.1885', '0.2158', '-0.4236', '0.1959', '-0.0753', '0.1604', '0.2092', '0.03333', '-0.0712', '0.0128', '-0.01122', '-0.1906', '0.02806', '-0.1917', '-0.2218', '0.3052', '0.1295', '-0.1554', '-0.2302', '-0.0346', '-0.4485', '0.5366', '-0.1119', '0.04846', '0.1619', '0.0974', '0.02759', '-0.0885', '-0.514', '0.0671', '0.3403', '0.5073', '0.2588', '-0.0933', '-0.503', '-0.658', '-0.1661', '-0.3582', '-0.2412', '-0.3662', '-0.3713', '0.2493', '-0.03632', '-0.5605', '-0.3906', '-0.2227', '-0.1616', '0.03546', '0.4104', '0.03674', '-0.2004', '0.08704', '0.1555', '-0.3079', '0.2051', '0.273', '-0.5317', '-0.04446', '0.2932', '-0.1225', '0.595', '-0.05685', '-0.02634', '0.62', '-0.011406', '0.322', '0.271', '-0.2015', '0.2491', '-0.1384', '-0.2051', '-0.05118', '-0.346', '0.1403', '0.001621', '0.5747', '-0.1718', '0.2406', '0.01938', '-0.03128', '0.05554', '0.01683', '-0.0899', '-0.1404', '-0.03108', '0.2095', '0.346', '0.4595', '-0.04227', '0.699', '0.368', '-0.2048', '-0.344', '0.824', '0.8438', '0.0816', '-0.513', '-0.10315', '-0.03284']",,,C563311,,,,
mondo:0011087,inflammatory bowel disease 2,"['inflammatory bowel disease 2', 'inflammatory bowel disease type 2', 'IBD2']",0110900,601458,,C1832321,,,,C563310,,,,
mondo:0011088,congenital myasthenic syndrome 1A,"['congenital myasthenic syndrome 1A, slow-channel', 'congenital myasthenic syndrome type 1A', 'CMS IIa', 'congenital myasthenic syndrome type IIa', 'CHRNA1 congenital myasthenic syndrome', 'congenital myasthenic syndrome caused by mutation in CHRNA1', 'CMS1A', 'myasthenic syndrome, congenital, type IIa, formerly', 'myasthenic syndrome, congenital, 1A, slow-channel', 'Cms IIa', 'Cms IIa, formerly', 'myasthenic syndrome, congenital, type IIa']",0110663,601462,,,,,,,,,,
mondo:0011089,patent ductus venosus,"['portosystemic Venous shunt, congenital', 'PDV', 'PSVS', 'patent ductus venosus']",,601466,,,,,,C562830,747.49,,,
mondo:0011090,isolated hereditary congenital facial paralysis,"['facial palsy, congenital, unilateral or bilateral', 'facial paresis hereditary congenital', 'hereditary congenital facial paresis', 'MBS2 (formerly)', 'Moebius syndrome 2 (formerly)', 'Mobius syndrome 2 (formerly)', 'facial paresis, hereditary congenital', 'HCFP']",,,306527,C4518577,,,,C563309,,,,
mondo:0011091,Charcot-Marie-Tooth disease type 2D,"['Charcot Marie Tooth disease type 2D', 'Charcot-Marie-Tooth disease, axonal, type 2D', 'Charcot-Marie-Tooth disease, neuronal, type 2D', 'GARS Charcot-Marie-Tooth disease type 2', 'Charcot-Marie-Tooth disease, type 2D', 'autosomal dominant Charcot-Marie-Tooth disease type 2D', 'Charcot-Marie-Tooth disease type 2 caused by mutation in GARS', 'CMT 2D', 'Charcot-Marie-Tooth neuropathy type 2D', 'Charcot-Marie-Tooth disease neuronal type 2D', 'CMT2D', 'Charcot-Marie-Tooth neuropathy, type 2D']",0110164,601472,99938,C4274109,"['0.1488', '0.1958', '0.271', '-0.1237', '-0.02429', '-0.39', '0.28', '0.748', '-0.7075', '-0.2488', '-0.0892', '0.4348', '-0.4907', '0.535', '-0.0831', '0.1051', '-0.04776', '-0.442', '-0.4116', '-0.753', '0.1776', '0.2382', '0.3975', '0.6416', '0.12384', '0.01828', '0.1357', '0.1236', '0.0679', '0.02228', '0.284', '-0.5547', '0.06128', '-0.12195', '0.1692', '-0.626', '-0.491', '-0.3284', '0.4705', '-0.03296', '-1.428', '-0.5356', '-0.3198', '0.2947', '-0.2446', '-0.2546', '0.4065', '-0.11066', '0.00467', '-0.08', '0.2003', '0.379', '-0.1891', '-1.099', '0.1964', '-0.2179', '-0.2983', '0.3254', '-1.027', '-0.3557', '-0.258', '-0.06714', '0.8135', '0.5825', '-0.6494', '1.166', '0.0848', '0.6436', '-0.7812', '0.3486', '-0.587', '-0.1137', '0.2925', '-0.1438', '1.195', '0.584', '-0.2795', '0.7246', '0.1449', '-0.5312', '-0.297', '-0.182', '0.878', '0.546', '0.06064', '-0.1925', '0.0682', '0.3975', '0.791', '0.2246', '0.2576', '-0.329', '-0.0753', '0.589', '0.5522', '0.6753', '0.644', '-0.819', '0.01675', '0.7266']",C122659,,C537993,,,,
mondo:0011092,ribbing disease,"['multiple diaphyseal sclerosis', 'diaphyseal sclerosis, multiple', 'ribbing disease', 'hereditary multiple diaphyseal sclerosis']",,601477,,C1832273,,,,C537613,,,,
mondo:0011093,mucopolysaccharidosis type 9,"['mucopolysaccharidosis IX', 'MPS 9', 'hyaluronidase deficiency', 'mucopolysaccharidosis, type 9', 'MPS9', 'mucopolysaccharidosis type IX', 'mucopolysaccharidosis type 9', 'mucopolysaccharidosis, type IX', 'MPSIX']",0050809,601492,67041,C1291490,"['-0.5293', '0.3086', '0.3706', '-0.3928', '0.4277', '-0.352', '-0.10406', '0.2927', '-0.664', '-0.2369', '0.2023', '0.3853', '0.07214', '-0.1895', '-0.3289', '0.1599', '0.1847', '-0.2133', '-0.4097', '-0.535', '0.3809', '-0.311', '0.584', '0.014984', '0.03574', '0.503', '0.3542', '0.1423', '0.1744', '-0.1798', '0.0214', '0.0256', '0.3503', '0.2332', '0.1953', '-0.2554', '-0.1312', '-0.281', '-0.02736', '-0.4502', '-0.09503', '-0.2103', '0.2556', '0.3723', '-0.07275', '-0.1394', '0.2397', '0.326', '0.288', '0.0744', '-0.1843', '-0.1148', '0.11523', '0.1895', '-0.09985', '-1.046', '-0.01744', '-0.2257', '-0.5483', '0.0377', '0.3945', '0.2172', '-0.2498', '-0.01793', '0.3416', '-0.05255', '0.2485', '-0.1917', '-0.002384', '-0.05615', '-0.6807', '-0.1012', '-0.004406', '0.01058', '-0.237', '0.4521', '0.3198', '0.418', '-0.1707', '-0.2169', '-0.03293', '-0.1499', '-0.1019', '0.2515', '0.1277', '0.1332', '0.2418', '0.3066', '0.2001', '0.1688', '-0.04642', '0.3228', '0.284', '-0.2427', '0.98', '0.2563', '0.392', '-0.1718', '0.4387', '0.1945']",C129073,,C563209,277.6,,,
mondo:0011094,dilated cardiomyopathy 1C,"['dilated cardiomyopathy 1C with or without left ventricular noncompaction', 'CMD1C', 'cardiomyopathy, dilated, 1C, with or without LVNC', 'CMDC1', 'dilated cardiomyopathy type 1C', 'cardiomyopathy, familial hypertrophic, 24', 'cardiomyopathy, hypertrophic, 24', 'left ventricular noncompaction 3', 'cardiomyopathy, dilated, 1C, with or without left ventricular noncompaction']",0110423,601493,,,,C170436,,C563307,,,,
mondo:0011095,dilated cardiomyopathy 1D,"['cardiomyopathy, dilated, type 1D', 'TNNT2 familial isolated dilated cardiomyopathy', 'dilated cardiomyopathy type 1D', 'left ventricular noncompaction 6', 'CMD1D', 'cardiomyopathy, dilated, 1D', 'familial isolated dilated cardiomyopathy caused by mutation in TNNT2']",0110426,601494,,C1832243,,,,C563306,,,,
mondo:0011096,autosomal agammaglobulinemia,"['agammaglobulinemia, autosomal recessive, due to IGHM defect', 'AGM', 'agammaglobulinemia, non-Bruton type']",,,33110,C1832241,"['0.551', '0.0686', '-0.5566', '-0.08417', '-0.006516', '-0.4153', '0.587', '0.1636', '-0.4612', '-0.052', '0.01563', '-0.12354', '-0.6025', '0.73', '0.02272', '-0.3123', '-0.005066', '0.5176', '-0.2559', '-0.7715', '-0.181', '-0.1176', '0.596', '-0.6465', '0.0721', '0.0549', '-0.596', '-0.2952', '-0.0818', '-0.4038', '0.4133', '0.5083', '0.03857', '0.01144', '-0.39', '0.2817', '-0.898', '-0.0641', '-0.066', '0.3298', '-0.4717', '-0.724', '0.3315', '-0.1978', '0.256', '-0.2314', '-0.4678', '-0.4233', '-0.2395', '0.1241', '0.08344', '0.2365', '0.2401', '-0.4429', '-0.1126', '0.373', '-0.2451', '-0.4116', '-0.508', '0.2227', '0.529', '0.816', '0.02997', '-0.03366', '0.537', '-0.1074', '0.5127', '0.4475', '-0.2362', '0.615', '-0.2223', '-0.0902', '-0.575', '-0.6753', '0.3152', '-0.158', '0.4126', '-0.422', '0.1898', '-0.1487', '-0.8755', '-0.2018', '0.2406', '0.263', '0.3794', '0.8423', '0.184', '0.323', '0.1089', '0.0916', '0.1608', '0.4644', '-0.2825', '-0.1583', '0.441', '1.134', '0.3833', '-0.464', '-0.654', '-0.1092']",,,C538056,,,,
mondo:0011097,Axenfeld-Rieger syndrome type 2,"['Axenfeld-Rieger syndrome, type 2', 'RIEG2', 'Rieger syndrome, type 2', 'Rieger syndrome type 2']",0110121,601499,,C1832229,,,,C535680,,,,
mondo:0011098,"prostate cancer, hereditary, 1","['prostate cancer 1', 'RNASEL familial prostate cancer', 'familial prostate cancer caused by mutation in RNASEL', 'HPC1', 'prostate cancer, hereditary, type 1', 'prostate cancer, hereditary, 1', 'Prca1']",,601518,,,,,,,,,,
mondo:0011099,human HOXA1 syndromes,"['ABDS', 'Human HOXA1 syndromes', 'Bosley Salih Alorainy syndrome', 'Athabaskan brainstem dysgenesis', 'Bosley-Salih-Alorainy syndrome', 'BSAS', 'Athabaskan brainstem dysgenesis syndrome', 'Navajo brainstem syndrome', 'ABSD', 'Athabascan brainstem dysgenesis syndrome']",0050682,601536,69739,C1832215,"['0.177', '0.1782', '0.1613', '-0.2142', '0.1671', '-0.44', '0.3083', '0.1604', '0.2764', '-0.5815', '-0.3376', '-0.6113', '-0.5215', '-0.1064', '0.01814', '0.4004', '0.04736', '-0.1337', '-0.2274', '-0.6265', '0.5312', '0.058', '-0.1829', '-0.1772', '-0.2834', '-0.2864', '0.2048', '-0.1211', '0.536', '-0.2627', '0.2893', '0.2642', '0.5137', '-0.2386', '-0.2632', '-0.1946', '-0.05823', '-0.06183', '-0.04422', '0.151', '0.1214', '-0.2717', '0.1447', '0.1171', '0.01159', '-0.0565', '-0.08765', '-0.0719', '-0.3997', '-0.02246', '-0.0938', '0.1422', '-0.0841', '-0.1682', '0.02998', '0.2129', '0.4663', '-0.01432', '0.2163', '0.1564', '0.2388', '-0.2212', '-0.1539', '0.4177', '-0.3384', '-0.1654', '-0.1121', '0.7954', '-0.782', '0.847', '-0.6743', '0.4832', '-0.2803', '-0.04706', '0.1377', '-0.08954', '0.57', '0.263', '-0.4558', '0.01947', '0.2416', '-0.127', '0.537', '1.332', '-0.0814', '-0.01866', '0.1986', '0.667', '0.1119', '0.1183', '0.6094', '0.304', '0.04446', '0.2632', '0.823', '-0.09674', '0.4946', '-0.2556', '0.06506', '0.10736']",,,,,,,
mondo:0011100,"microcephaly, retinitis pigmentosa, and sutural cataract","['microcephaly, retinitis pigmentosa, and sutural cataract']",,601537,,C1832214,,,,C563296,,,,
mondo:0011101,peroxisome biogenesis disorder 1B,"['peroxisome biogenesis disorder (neonatal adrenoleukodystrophy/infantile Refsum disease)', 'peroxisome biogenesis disorder type 1B', 'peroxisome biogenesis disorder 1B', 'infantile phytanic acid storage disease', 'adrenoleukodystrophy, autosomal neonatal', 'peroxisome biogenesis disorder 1B (NALD/IRD)', 'PBD1B', 'Refsum disease, infantile', 'peroxisome biogenesis disorder (NALD/Ird)']",0081240,601539,772,CN168921,"['0.2644', '0.4368', '0.2864', '0.05167', '-0.1868', '-0.00881', '-0.1786', '0.8633', '-0.2935', '0.1852', '0.0387', '-0.6924', '-0.57', '0.6133', '-0.1846', '-1.096', '-0.2255', '-0.1659', '-0.6396', '-0.1418', '-0.0701', '-0.9185', '0.2812', '-0.0387', '-0.11536', '-0.304', '-0.4275', '0.1837', '-0.07275', '0.2317', '0.1512', '-0.2472', '0.259', '0.0389', '-0.6094', '0.03488', '-0.1032', '-0.707', '0.0988', '-0.2913', '-0.1694', '-0.1742', '0.2573', '-0.1914', '-0.137', '-0.07666', '0.2764', '-0.4414', '0.1144', '0.6816', '0.1969', '-0.01244', '0.2878', '-0.2842', '0.0438', '-0.6274', '0.2625', '-0.566', '-0.262', '0.88', '0.281', '-0.44', '0.4817', '0.4211', '-0.014694', '0.13', '0.3828', '0.00535', '-0.358', '-0.1422', '-0.3164', '0.0314', '0.3076', '-0.2094', '0.1906', '0.2922', '0.648', '-0.545', '-0.317', '-0.2288', '0.0714', '-0.4485', '-0.9434', '0.4988', '-0.4155', '0.411', '0.00499', '-0.505', '1.045', '0.298', '0.711', '0.669', '-0.4614', '0.536', '-0.2113', '0.2064', '0.3289', '-0.05023', '0.536', '0.1172']",C155749,,,,,,
mondo:0011102,autosomal dominant nonsyndromic hearing loss 12,"['autosomal dominant nonsyndromic deafness type 12', 'deafness, autosomal dominant 8/12', 'autosomal dominant nonsyndromic deafness caused by mutation in TECTA', 'autosomal dominant nonsyndromic deafness 12', 'deafness, autosomal dominant type 12', 'deafness, autosomal dominant 12', 'TECTA autosomal dominant nonsyndromic deafness', 'autosomal dominant deafness 12', 'DFNA8', 'deafness, autosomal dominant 8', 'autosomal dominant deafness 8', 'DFNA12']",0110544,601543,,C1832187,,,,C563295,,,,
mondo:0011103,autosomal dominant nonsyndromic hearing loss 3A,"['autosomal dominant nonsyndromic deafness type 3A', 'DFNA3', 'deafness, autosomal dominant 3a', 'DFNA3A', 'autosomal dominant nonsyndromic deafness caused by mutation in GJB2', 'deafness, autosomal dominant nonsyndromic sensorineural 3', 'deafness, autosomal dominant 3A', 'autosomal dominant nonsyndromic deafness 3A', 'GJB2 autosomal dominant nonsyndromic deafness', 'autosomal dominant deafness 3A', 'neurosensory nonsyndromic dominant deafness 1', 'deafness, autosomal dominant type 3A', 'NSRD1']",0110564,601544,,C2675750,,,,C567277,,,,
mondo:0011104,cataract 3 multiple types,"['cataract 3 multiple types with or without microcornea', 'cataract 3, multiple types', 'cataract, congenital, cerulean type, 2', 'congenital cerulean type cataract 2', 'CTRCT3', 'CRYBB2 cataract (disease)', 'CCA2', 'cataract 3, multiple types, with or without microcornea']",0110269,601547,98994,C1832175,"['-0.2537', '0.1375', '0.01953', '0.1912', '0.0311', '-0.1467', '0.010345', '0.398', '-0.2537', '-0.232', '-0.0831', '-0.249', '-0.1079', '0.1655', '-0.185', '-0.2401', '0.089', '-0.1676', '0.1343', '-0.4587', '0.082', '0.02509', '0.06824', '-0.09894', '0.08246', '0.005997', '-0.03204', '0.1007', '-0.04895', '0.2152', '0.1636', '-0.2286', '0.1598', '0.2585', '0.0678', '0.05838', '0.1514', '-0.13', '-0.1177', '-0.252', '0.334', '-0.1538', '-0.02997', '0.10065', '-0.04626', '-0.1881', '0.03754', '-0.0744', '0.1531', '0.06854', '0.2264', '-0.00399', '0.1313', '0.0863', '-0.08246', '-0.2089', '0.3958', '-0.0478', '-0.2524', '-0.04398', '0.2067', '-0.223', '0.01041', '0.1832', '-0.1896', '0.09265', '0.436', '0.4075', '0.05804', '0.1908', '-0.2482', '0.2153', '0.2493', '0.0516', '-0.06384', '0.1543', '0.1436', '-0.0227', '-0.2666', '-0.1097', '-0.1575', '0.1204', '-0.1654', '0.222', '0.10504', '-0.1876', '0.0731', '0.1078', '0.18', '0.1647', '0.1428', '0.3232', '0.09393', '0.03928', '0.2727', '-0.1359', '0.306', '-0.2212', '0.1968', '0.06116']",,,C563294,,,,
mondo:0011105,"alacrima, congenital, autosomal recessive","['alacrima, congenital, autosomal recessive']",,601549,,C4012597,,,,,,,,
mondo:0011106,facial dysmorphism-lens dislocation-anterior segment abnormalities-spontaneous filtering blebs syndrome,"['FDLAB syndrome', 'facial dysmorphism-lens dislocation-anterior segment abnormalities-nontraumatic conjunctive cysts syndrome', 'facial dysmorphism, lens dislocation, anterior segment abnormalities, and spontaneous filtering blebs', 'FDLAB', 'Traboulsi syndrome', 'ectopia lentis, spontaneous filtering blebs, and craniofacial Dysmorphism']",,601552,412022,C1832167,,,,C563293,,,,
mondo:0011107,congenital hypotrichosis with juvenile macular dystrophy,"['HJMD', 'juvenile macular dystrophy and congenital hypotrichosis', 'Hjmd', 'juvenile macular degeneration and hypotrichosis', 'hypotrichosis with juvenile macular dystrophy', 'hypotrichosis, congenital, with juvenile macular dystrophy', 'hypotrichosis with cone-rod dystrophy', 'hypotrichosis with juvenile macular degeneration']",0110711,601553,1573,C1832162,"['0.09204', '0.2256', '-0.002317', '0.287', '0.5312', '-0.586', '0.1108', '0.696', '-0.0702', '-0.774', '0.602', '0.00735', '0.006058', '0.4385', '0.1256', '-0.4312', '0.6064', '-0.3433', '-0.2236', '-1.302', '-0.885', '-0.527', '0.2399', '-0.3113', '-0.0847', '0.3313', '-0.8896', '0.2006', '-0.3237', '-0.01617', '0.7227', '-0.264', '-0.2024', '0.014496', '0.2086', '0.707', '0.1926', '-0.5176', '-0.565', '0.2922', '0.503', '0.155', '0.3784', '-0.436', '0.4436', '0.393', '-0.2722', '-0.0304', '-0.1619', '-0.3433', '0.3892', '0.2009', '0.416', '0.1153', '0.1029', '-0.2698', '-0.0637', '-0.4963', '-0.4963', '0.04672', '-0.0826', '0.4148', '0.6475', '-0.3477', '0.1065', '0.1857', '0.3198', '0.5186', '-0.05984', '0.682', '-0.05182', '-0.74', '0.1288', '0.1393', '-0.0926', '-0.55', '0.05447', '-0.2944', '-0.6357', '0.064', '0.687', '-0.1469', '0.1015', '0.5356', '0.05344', '0.02663', '-0.3071', '-0.00848', '0.634', '0.351', '0.125', '0.478', '-0.1117', '0.2688', '0.3684', '-0.524', '0.3193', '-0.4695', '0.2842', '0.3533']",,,C537698,,,,
mondo:0011109,"multiple epiphyseal dysplasia, Lowry type","['multiple epiphyseal dysplasia with ROBIN phenotype', 'epiphyseal dysplasia, multiple, with Robin phenotype', 'multiple epiphyseal dysplasia with Robin phenotype']",,601560,166016,C1832112,,,,C563291,,,,
mondo:0011110,dyssegmental dysplasia-glaucoma syndrome,"['dyssegmental dysplasia and glaucoma', 'dyssegmental dysplasia with glaucoma']",,601561,1804,C1832111,,,,C563290,,,,
mondo:0011112,Wilms tumor 5,"['Wilms tumor type 5', 'Wilms tumor and radial bilateral aplasia', 'Wilms tumour type 5', 'Wilms tumour susceptibility-5, autosomal dominant, somatic mutation', 'Wilms tumor susceptibility-5, autosomal dominant, somatic mutation', 'Wilms tumour and radial bilateral aplasia', 'Wilms tumor 5', 'bilateral radial aplasia with Wilms tumour', 'WT5', 'Wilms tumor, susceptibility to', 'bilateral radial aplasia with Wilms tumor']",,601583,,,,,,C536707,,,,
mondo:0011113,Charcot-Marie-Tooth disease type 4C,"['CMT 4C', 'SH3TC2 Charcot-Marie-Tooth disease type 4', 'autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4C', 'Charcot-Marie-Tooth disease, demyelinating, autosomal recessive, type 4C', 'Charcot-Marie-Tooth neuropathy, type 4C', 'Charcot-Marie-Tooth neuropathy type 4C', 'CMT4C', 'Charcot-Marie-Tooth disease type 4 caused by mutation in SH3TC2', 'Charcot-Marie-Tooth disease, type 4C', 'Charcot Marie Tooth disease type 4C']",0110183,601596,99949,C1866636,"['0.00844', '0.2056', '0.0704', '-0.1586', '-0.16', '-0.2903', '0.02348', '0.6045', '-0.412', '-0.263', '-0.01233', '0.3442', '-0.6235', '0.397', '-0.1581', '-0.015045', '-0.202', '-0.648', '-0.4082', '-0.4248', '0.0653', '0.1764', '0.2817', '0.5176', '0.4917', '0.593', '-0.00426', '0.2179', '0.1768', '-0.144', '0.1648', '-0.6616', '0.07306', '0.02899', '0.1984', '-0.565', '-0.375', '-0.4224', '0.4875', '-0.011314', '-1.569', '-0.6807', '-0.3125', '0.2203', '-0.2615', '-0.0988', '-0.04013', '0.0937', '-0.5034', '-0.1547', '0.0535', '0.2783', '-0.427', '-1.062', '0.567', '-0.2231', '0.3044', '0.03156', '-0.3054', '0.07764', '-0.1587', '0.025', '0.4194', '0.572', '-0.448', '1.038', '0.00828', '0.559', '-0.3943', '0.4817', '-0.7534', '0.3743', '0.5796', '0.03226', '0.7017', '0.941', '-0.7427', '0.6143', '-0.04538', '-0.4626', '-0.01303', '-0.1581', '0.3762', '0.8867', '0.1187', '-0.01704', '0.3523', '0.704', '0.769', '0.3916', '0.1556', '-0.06097', '0.3179', '0.429', '0.515', '0.4644', '0.6553', '-0.3423', '0.05194', '0.04636']",C129864,,C535423,,,,
mondo:0011114,familial multiple trichoepithelioma,"['epithelioma adenoides cysticum', 'Brooke-Fordyce Trichoepitheliomas', 'epithelioma Adenoides Cysticum of Brooke', 'epithelioma, hereditary multiple benign cystic', 'trichoepithelioma multiple familial', 'multiple familial trichoepithelioma', 'hereditary multiple benign cystic epithelioma']",,,867,C1275122,"['-0.05228', '0.0787', '0.000264', '-0.03806', '0.01081', '-0.1109', '0.0165', '0.1142', '-0.1007', '-0.03073', '0.02124', '-0.004684', '-0.008575', '0.01805', '-0.0517', '-0.05273', '-0.02249', '-0.0189', '0.002415', '-0.1702', '-0.005257', '-0.03738', '0.0855', '-0.0643', '0.03125', '-0.00711', '-0.02098', '-0.02702', '0.00593', '-0.0574', '0.09094', '-0.004837', '0.1137', '0.05334', '0.01677', '-0.0573', '-0.0488', '-0.04034', '-0.01678', '-0.0928', '0.0643', '-0.0933', '0.06195', '-0.0825', '0.04562', '-0.10583', '-0.05994', '0.08954', '-0.0002127', '0.02216', '-0.02756', '-0.004494', '0.03934', '0.02325', '-0.10156', '-0.01859', '0.0703', '-0.0504', '-0.1399', '-0.02094', '0.11584', '0.03946', '-0.0005455', '0.01286', '-0.01269', '0.0613', '0.1268', '0.08795', '-0.0897', '0.09735', '-0.02812', '0.01767', '0.0072', '-0.0708', '0.042', '0.04407', '0.0128', '0.05072', '-0.07153', '-0.07697', '-0.011116', '0.06052', '-0.03915', '0.09314', '-0.02309', '-0.005554', '0.0392', '0.0715', '0.09656', '0.01674', '0.04663', '0.06274', '0.00851', '0.02087', '0.1936', '0.0473', '0.1073', '-0.1367', '-0.02171', '0.02516']",,,,,,,
mondo:0011115,spastic paraplegia and Evans syndrome,['spastic paraplegia and Evans syndrome'],,601608,,C1866619,,,,C566652,,,,
mondo:0011116,lung agenesis-heart defect-thumb anomalies syndrome,"['Mardini-Nyhan syndrome', 'lung agenesis heart defect thumb anomalies', 'Mardini-Nyhan association', 'Manouvrier syndrome', 'pulmonary aplasia and triphalangia of the thumb', 'lung agenesis, congenital heart defects, and thumb anomalies syndrome', 'LACHT']",,601612,1120,C0265780,,,,C535708,,,,
mondo:0011117,iris pigment epithelium anomalies,"['cysts of iris pigment epithelium', 'iris pigment epithelium anomalies', 'ruffles and cysts of iris pigment epithelium']",,601616,,C1866608,,,,C566651,,,,
mondo:0011118,bilineal acute myeloid leukemia,"['acute bilineal leukaemia', 'bilineal acute leukaemia', 'acute bilineal leukemia', 'bilineal acute leukemia']",,,98836,C0349680,,C6923,,,,,,
mondo:0011119,iridogoniodysgenesis,['IRID'],0050786,,98634,,,,,,,,,
mondo:0011120,"neural tube defects, folate-sensitive","['NTDFS', 'spina bifida, folate-sensitive', 'neural tube defects, folate-sensitive', 'neural tube defects, susceptibility to', 'NTD, folate-sensitive', 'neural tube defects, folate-sensitive, susceptibility to']",,601634,,C1866558,,,,C536409,,,,
mondo:0011121,paragangliomas 2,"['paragangliomas 2', 'paraganglioma caused by mutation in SDHAF2', 'SDHAF2-related hereditary paraganglioma-pheochromocytoma syndrome (paragangliomas 2)', 'glomus tumors, familial, 2', 'SDHAF2 paraganglioma', 'PGL2', 'paragangliomas type 2']",,601650,,,,,,C566646,,,,
mondo:0011122,obesity disorder,['obesity'],9970,,521399,C0028754,"['-0.07654', '0.4414', '-0.1647', '0.8193', '0.02185', '-0.649', '0.02335', '0.5454', '-0.3618', '-0.5796', '-0.1192', '0.1697', '0.3777', '0.3135', '-0.673', '-0.645', '-0.363', '0.946', '-0.4453', '-0.797', '-0.04617', '-0.2435', '0.3333', '-0.4277', '0.0681', '0.11395', '-0.4336', '-0.605', '0.2869', '-0.4531', '0.4153', '-0.5186', '0.3816', '0.04712', '-0.159', '-0.4636', '-0.6284', '0.2206', '0.4805', '0.02666', '0.05328', '-0.06', '-0.974', '0.3867', '0.0755', '-0.655', '0.576', '0.1192', '0.37', '0.2332', '-0.5396', '0.03604', '0.552', '-0.2449', '-0.2339', '0.5693', '-0.2402', '-0.02963', '0.0751', '-0.5146', '0.519', '0.363', '-0.2235', '-0.6343', '-0.0674', '0.583', '-0.515', '0.3848', '0.256', '0.5728', '0.1934', '0.4517', '-0.01227', '-0.4446', '0.604', '-0.3726', '-0.2925', '-0.01407', '-1.216', '0.348', '-0.0862', '0.765', '0.1757', '0.11237', '0.998', '0.7944', '0.2063', '0.1652', '0.8154', '0.5063', '-0.24', '0.2954', '-0.4033', '0.646', '0.8164', '0.1421', '0.1137', '-0.3567', '-0.3625', '-0.1279']",C3283,0001073,,278.00,,,0001513
mondo:0011123,type 1 diabetes mellitus 15,"['insulin-dependent diabetes mellitus 15', 'IDDM15', 'diabetes mellitus, insulin-dependent, 15']",0110753,601666,,C1866519,,,,C566645,,,,
mondo:0011124,spondyloepimetaphyseal dysplasia-abnormal dentition syndrome,"['spondyloepimetaphyseal dysplasia with abnormal dentition', 'SEMDAD']",,601668,168451,C1866507,,,,C566644,,,,
mondo:0011125,"trichothiodystrophy 1, photosensitive","['TTD1', 'Tay syndrome', 'ichthyosiform erythroderma with hair Abnormality and mental and Growth retardation', 'trichothiodystrophy 1, photosensitive', 'trichothiodystrophy with congenital ichthyosis', 'trichothiodystrophy, photosensitive', 'PIBIDS syndrome']",0111873,601675,670,,,C156433,,,,,,
mondo:0011126,acute insulin response,"['Air', 'acute insulin response']",,601676,,,,,,,,,,
mondo:0011128,Sheldon-hall syndrome,"['DA2B', 'Sheldon-Hall syndrome', 'distal arthrogryposis type 2B', 'Freeman Sheldon syndrome, variant', 'Freeman Sheldon variant', 'arthrogryposis multiplex congenita distal type 2B', 'arthrogryposis multiplex congenita, distal, type 2B', 'Freeman-Sheldon syndrome variant', 'arthrogryposis, distal, type 2B', 'arthrogryposis multiplex congenita distal type II with craniofacial abnormalities', 'arthrogryposis multiplex congenita, distal, type II, with craniofacial abnormalities']",0111599,,1147,C1834523,"['0.11334', '-0.1498', '-0.2825', '0.01023', '0.06287', '-0.742', '0.59', '0.633', '-0.884', '-0.5576', '0.0823', '0.01582', '0.05716', '0.1127', '-0.2396', '0.3962', '0.445', '-0.2242', '-0.1575', '-0.4275', '-0.1562', '-0.1747', '0.3093', '0.0442', '0.0783', '-0.2084', '-0.2488', '0.1853', '0.3438', '-0.2356', '0.3965', '-0.1647', '-0.042', '0.627', '0.0926', '-0.4548', '-0.01432', '-0.1619', '0.2698', '-0.12396', '0.1181', '-0.592', '-0.17', '-0.2266', '0.5234', '-0.2275', '-0.02519', '0.8643', '0.2197', '-0.2291', '-0.5093', '-0.552', '-0.06113', '-0.113', '-0.8003', '-0.2908', '-0.0671', '-0.5103', '0.1545', '0.04657', '0.3384', '0.1854', '-0.568', '0.123', '-0.2644', '-0.1262', '0.256', '0.2664', '-0.1711', '0.387', '-0.2917', '0.2303', '-0.124', '-0.1412', '0.0862', '0.3247', '0.0732', '-0.584', '-0.4358', '0.1256', '0.2705', '-0.1589', '-0.04147', '0.9053', '-0.518', '0.622', '-0.4197', '0.2461', '-0.0871', '0.09607', '0.2583', '0.2114', '0.0823', '0.265', '0.6235', '-0.4873', '0.7656', '-0.4885', '0.175', '-0.3088']",,,,,,,
mondo:0011129,glaucoma type 1C,"['glaucoma 1, primary open angle, C', 'GLC1C', 'glaucoma 1C, primary open angle']",,601682,,C1866483,,,,,,,,
mondo:0011130,"sebaceous gland hyperplasia, familial presenile","['sebaceous gland hyperplasia, familial presenile']",,601700,,C1866428,,,,C537530,,,,
mondo:0011131,tricho-oculo-dermo-vertebral syndrome,"['Alves-dos Santos-Castelo syndrome', 'ectodermal dysplasia-cataracts-kyphoscoliosis syndrome', 'Trichooculodermovertebral syndrome', 'Alves syndrome', 'ectodermal dysplasia - cataracts - kyphoscoliosis', 'arthrogryposis and ectodermal dysplasia', 'Todv syndrome']",,601701,3354,,,,,C537441,,,,
mondo:0011132,"T-cell immunodeficiency, congenital alopecia, and nail dystrophy","['congenital alopecia and nail dystrophy associated with severe functional T-cell immunodeficiency', 'Pignata Guarino syndrome', 'FOXN1 deficiency', 'T-cell immunodeficiency, congenital alopecia and nail dystrophy', 'severe T-cell immunodeficiency-congenital alopecia-nail dystrophy syndrome', 'T-cell immunodeficiency, congenital alopecia, and nail dystrophy', 'alymphoid cystic thymic dysgenesis', 'winged helix deficiency']",0060769,601705,169095,C1866426,"['-0.8984', '-0.04648', '0.281', '-0.236', '0.6587', '-0.5723', '-0.2435', '-0.1278', '-0.2006', '-0.1342', '0.00413', '-0.154', '-0.3413', '0.2241', '-0.01002', '0.1796', '0.439', '-0.1317', '-0.433', '-0.6035', '-0.1023', '-0.06793', '0.5186', '-0.08813', '0.3423', '-0.0978', '-0.4531', '0.04868', '0.0781', '-0.4797', '0.3923', '0.651', '0.095', '0.2384', '0.3325', '-0.3152', '-0.351', '0.2405', '-0.3474', '-0.3862', '0.02313', '0.2622', '-0.3525', '-0.0516', '-0.7534', '-0.2175', '-0.11566', '-0.285', '0.24', '-0.1788', '-0.2502', '-0.1687', '0.713', '0.4407', '-0.649', '-0.2925', '0.2175', '-0.1893', '-0.013954', '-0.076', '0.05554', '0.352', '-0.04678', '0.1091', '0.533', '0.1373', '0.3628', '0.734', '-0.267', '0.2495', '-0.45', '-0.0926', '0.11017', '-0.1069', '-0.2449', '-0.337', '0.3914', '-0.0988', '0.1787', '0.2018', '0.128', '-0.05716', '-0.1641', '-0.328', '-0.0483', '-0.3936', '0.001035', '0.4075', '0.1426', '0.379', '-0.0911', '0.368', '-0.07794', '0.2128', '0.7417', '0.2715', '-0.0813', '-0.6514', '0.3374', '0.3604']",,,C536781,,,,
mondo:0011133,"deaf blind hypopigmentation syndrome, Yemenite type","['Yemenite (Warburg) deaf-blind hypopigmentation syndrome', 'Warburg-Thomsen syndrome', 'Yemenite deaf-blind hypopigmentation syndrome', 'Warburg Thomsen syndrome']",,601706,3214,C1866425,,,,C536771,,,,
mondo:0011134,Curry-Jones syndrome,"['curry-Jones syndrome', 'corpus callosum agenesis polysyndactyly', 'curry Jones syndrome', 'CRJS', 'Curry-Jones syndrome, somatic mosaic', 'craniofacial malformations, asymmetric, with polysyndactyly and abnormal skin and gut development', 'corpus callosum agenesis-polysyndactyly syndrome', 'curry-JONES syndrome']",,601707,1553,C0795915,"['-0.436', '-0.182', '0.633', '-0.678', '0.417', '-0.1866', '-0.1993', '0.02335', '0.1348', '0.0002003', '-0.6836', '-0.2559', '-0.0746', '-0.4688', '-0.3884', '0.02617', '0.2673', '-0.1038', '-0.323', '-1.211', '0.287', '-0.08813', '0.172', '-0.542', '0.1447', '-0.1577', '-0.643', '0.3293', '1.092', '0.1676', '-0.05624', '-0.8467', '0.0858', '-0.191', '0.4636', '0.168', '-0.2563', '0.4065', '-0.4165', '0.237', '0.0676', '-0.4', '-0.1169', '-0.2166', '0.2842', '-0.4001', '-0.211', '-0.1633', '0.2048', '0.0643', '-0.2189', '-0.1678', '0.1385', '0.2319', '-0.986', '-0.194', '0.01088', '0.002253', '-0.666', '-0.381', '-0.3225', '-0.2432', '0.06396', '0.089', '-0.2517', '0.01019', '-0.2788', '0.901', '-0.1348', '0.6978', '0.1412', '0.2935', '0.195', '-0.3005', '-0.1073', '-0.1256', '0.3835', '-0.1434', '-0.5063', '-1.086', '0.226', '-0.0761', '0.1863', '0.5425', '-0.0891', '-0.2754', '-0.1816', '0.545', '-0.08875', '0.06854', '0.1478', '0.7393', '0.3342', '0.1572', '0.855', '0.3384', '0.09796', '-0.4165', '0.823', '0.3164']",,,C536735,,,,
mondo:0011135,"superior transverse scapular ligament, calcification of, familial","['superior transverse scapular ligament, calcification of, familial']",,601708,,C1866424,,,,C566638,,,,
mondo:0011136,Quebec platelet disorder,"['QPD', 'factor V Quebec', 'platelet-type bleeding disorder 5', 'factor 5 Quebec', 'Quebec platelet disorder', 'bleeding disorder, platelet-type, 5', 'BDPLT5']",0111050,601709,220436,C1866423,"['-0.4067', '-0.1306', '-0.0384', '-0.2522', '-0.1189', '-0.001741', '0.02196', '0.2157', '-0.1022', '0.0456', '-0.02718', '0.2347', '0.2087', '0.00779', '-0.0494', '-0.10455', '-0.02438', '0.03162', '0.03223', '-0.3708', '-0.1221', '-0.1816', '0.2893', '-0.2495', '-0.05978', '-0.2051', '0.07806', '0.03763', '0.02834', '-0.1257', '-0.09753', '-0.07135', '0.1981', '0.2083', '-0.2028', '-0.1521', '-0.1403', '-0.1165', '0.0698', '-0.1813', '0.055', '-0.11743', '0.1106', '-0.1713', '-0.002157', '-0.0504', '-0.247', '0.12054', '0.10815', '0.09595', '-0.0645', '-0.146', '0.11395', '0.2317', '-0.09436', '0.02391', '0.2251', '-0.1161', '-0.2269', '-0.07825', '-0.01785', '0.179', '-0.03044', '-0.1453', '0.1914', '0.147', '0.2073', '-0.06683', '-0.2119', '0.2573', '-0.2642', '-0.07574', '-0.1748', '-0.2253', '0.1483', '-0.08563', '0.3215', '-0.0625', '0.03873', '-0.0666', '-0.2207', '-0.06396', '-0.1598', '0.3235', '-0.1918', '0.2908', '0.21', '0.2808', '0.3413', '-0.2688', '0.07874', '0.445', '0.0921', '-0.01918', '0.3315', '0.1724', '0.2367', '-0.2612', '-0.0282', '0.0714']",,,C536260,,,,
mondo:0011137,retinitis pigmentosa 19,"['retinitis pigmentosa type 19', 'retinitis pigmentosa caused by mutation in ABCA4', 'retinitis pigmentosa 19', 'ABCA4 retinitis pigmentosa', 'RP 19', 'RP19']",0110354,601718,,C1866422,,,,C566637,,H35.5,,
mondo:0011138,"systemic lupus erythematosus, susceptibility to, 1","['susceptibility to systemic lupus erythematosus 1', 'SLEB1', 'systemic lupus erythematosus, susceptibility to, type 1', 'systemic lupus erythematosus, resistance to, 1', 'systemic lupus erythematosus, resistance to', 'TLR5 systemic lupus erythematosus (disease)', 'systemic lupus erythematosus, susceptibility to, 1']",,601744,,,,,,,,,,
mondo:0011139,preaxial hallucal polydactyly,['preaxial hallucal polydactyly'],,601759,,C1866339,,,,C566632,,,,
mondo:0011141,"megaloblastic anemia, folate-responsive","['MEGAF', 'folate level in erythrocytes']",,601775,,C2749656,,,,,,,,
mondo:0011142,"Ehlers-Danlos syndrome, musculocontractural type","['ATCS', 'EDSMC', 'Ehlers-Danlos syndrome, arthrogryposic type', 'Ehlers-Danlos syndrome, musculocontractural type 1', 'musculocontractural Ehlers-Danlos syndrome', 'arthrogryposis, distal, with peculiar facies and hydronephrosis', 'EDSMC1', 'D4ST1-deficient EDS', 'adducted thumb, clubfoot, and progressive joint and skin laxity syndrome', 'Ehlers-Danlos syndrome, Kosho type', 'MCEDS', 'adducted thumb-club foot syndrome', 'Dundar syndrome', 'EDS6B, formerly', 'adducted thumbs-arthrogryposis syndrome, Dundar type', 'adducted thumb-clubfoot syndrome', 'adducted thumb clubfoot syndrome', 'musculocontractural EDS', 'adducted thumbs Dundar type', 'EDS, arthrogryposic type', 'Ehlers-Danlos syndrome, musculocontractural type, 1', 'Ehlers-Danlos syndrome, type Vib, formerly', 'autosomal recessive adducted thumb-club foot syndrome', 'CHST14-related EDS', 'EDS, Kosho type', 'EDSmc', 'D4ST1-deficient Ehlers-Danlos syndrome', 'Ehlers-Danlos syndrome, type Vib', 'CHST14-related Ehlers-Danlos syndrome', 'EDS, musculocontractural type', 'Ehlers-Danlos syndrome, type VIB, formerly']",,,2953,,"['0.3464', '0.03668', '-0.5747', '0.2151', '0.343', '-0.612', '-0.0669', '0.4797', '-1.0625', '0.4163', '0.0713', '-0.12317', '0.07764', '0.835', '-0.5815', '0.302', '-0.7305', '0.36', '0.2024', '-0.4026', '0.1582', '1.056', '0.638', '-0.02463', '-0.1553', '0.3726', '0.0756', '0.2225', '1.34', '0.3142', '1.155', '-0.517', '0.2211', '0.0934', '-0.0246', '-0.3635', '-0.3052', '0.0518', '0.422', '-0.9146', '0.6196', '-0.141', '-0.5938', '0.07733', '0.04697', '-0.743', '-0.4072', '1.032', '0.6616', '-0.508', '-0.0675', '-0.5015', '0.5737', '-0.3286', '0.182', '-0.717', '-0.6904', '0.773', '0.1985', '-0.05338', '0.1101', '0.3384', '0.0956', '0.0843', '0.1272', '0.1486', '-0.12256', '0.9116', '-0.188', '0.973', '-0.728', '0.3235', '-0.55', '-0.2834', '-0.2336', '-0.3196', '-0.509', '-0.011215', '-0.00497', '-0.2113', '-0.08356', '-0.4758', '0.2021', '0.7246', '-0.8774', '0.1301', '0.0869', '0.616', '-0.10516', '0.1212', '0.83', '0.7075', '-0.4019', '0.3533', '0.769', '-0.08575', '0.741', '-0.09344', '0.2045', '-0.0706']",,,C000600608,,,,
mondo:0011143,cone-rod dystrophy 6,"['cone-rod dystrophy type 6', 'CORD6', 'retinal cone dystrophy 2', 'GUCY2D cone-rod dystrophy', 'RCD2', 'cone-rod dystrophy 6', 'cone-rod dystrophy caused by mutation in GUCY2D']",0111011,601777,,C1866293,,,,C538363,,,,
mondo:0011144,"ceroid lipofuscinosis, neuronal, 6A","['CLN6 late infantile neuronal ceroid lipofuscinosis', 'neuronal ceroid lipofuscinosis type 6', 'CLN6 disease, adult Kufs type A (subtype)', 'ceroid lipofuscinosis, neuronal, 6, variable age at onset', 'ceroid lipofuscinosis, neuronal, type 6', 'CLN6', 'ceroid lipofuscinosis, neuronal, 6', 'CLN6A', 'neuronal ceroid lipofuscinosis, Gypsy/Indian early juvenile variant', 'vLINCL', 'CLN6 disease, late infantile (subtype)', 'CLN6 disease', 'neuronal ceroid lipofuscinosis, late infantile, variant', 'neuronal ceroid lipofuscinosis 6 variable age of onset', 'late infantile neuronal ceroid lipofuscinosis caused by mutation in CLN6', 'neuronal ceroid lipofuscinosis 6']",0110729,601780,228363,,"['0.2067', '0.3809', '0.05518', '0.0992', '-0.07556', '-0.673', '-0.05975', '0.05698', '-0.0983', '-0.181', '-0.0819', '-0.12177', '-0.2335', '0.02931', '0.4023', '-0.1074', '-0.313', '-0.3801', '-0.2261', '-0.1354', '-0.1754', '-0.3818', '-0.2673', '0.00781', '0.2253', '-0.454', '-0.06183', '-0.2715', '-0.6255', '0.1709', '0.5737', '-0.10236', '0.3213', '-0.121', '0.4646', '-0.10736', '-0.0765', '-0.185', '-0.242', '-0.02965', '-0.1711', '-0.4531', '0.08325', '-0.006718', '0.1626', '-0.4407', '-0.0544', '0.0625', '0.1001', '0.4377', '-0.1514', '0.2812', '-0.2037', '-0.3347', '0.508', '-0.09595', '0.12195', '0.322', '-0.3228', '0.3796', '0.001042', '0.0714', '0.3274', '0.278', '-0.455', '0.2499', '0.2578', '0.07733', '-0.2334', '0.2234', '0.1656', '-0.09717', '-0.08246', '0.103', '0.4746', '0.3494', '0.3792', '0.1732', '-0.3643', '-0.3193', '0.4885', '-0.3262', '0.0249', '0.2815', '0.1721', '-0.04883', '0.1854', '0.10254', '0.3174', '0.0895', '-0.0829', '0.0965', '-0.07306', '-0.1351', '0.4265', '0.2325', '0.4177', '-0.1992', '0.1667', '-0.1918']",,,C566627,,,,
mondo:0011145,colobomatous microphthalmia - obesity - hypogenitalism - intellectual disability syndrome,"['coloboma-obesity-hypogenitalism-mental retardation syndrome', 'coloboma-obesity-hypogenitalism-intellectual disability syndrome']",,601794,363741,C1866256,,,,C566623,,,,
mondo:0011146,tetrasomy 12p,"['PKS', 'Hexasomy 12P, Mosaic', 'Killian syndrome', 'Teschler-Nicola Killian syndrome', 'chromosome 12, Isochromosome 12p syndrome', 'Killian Teschler-Nicola syndrome', 'Pallister-Killian mosaic syndrome', 'Isochromosome 12P syndrome', 'Isochromosome 12p syndrome', 'Isochromosome 12p mosaicism', 'Pallister Killian syndrome', 'Pallister-Killian syndrome', 'Pallister mosaic syndrome', 'tetrasomy type 12p', 'tetrasomy 12P, Mosaic', 'Pallister-Killian syndrome, Somatic mosaicism']",,601803,884,C0265449,,C75458,,C538105,758.81,,,
mondo:0011147,chromosome 18q deletion syndrome,"['partial monosomy of the long arm of chromosome 18', 'proximal 18q deletion syndrome', '18q deletion syndrome', 'chromosome 18q deletion', 'monosomy type 18q', 'monosomy 18q syndrome', '18Q syndrome', 'proximal 18q-', '18q-syndrome', 'deletion 18q syndrome', 'partial deletion of the long arm of chromosome 18', '18Q- syndrome', 'partial deletion of the long arm of chromosome type 18', 'chromosome 18Q- syndrome', 'proximal 18q deletion', 'monosomy 18q', 'partial monosomy of chromosome 18q', 'chromosome 18q deletion syndrome', 'proximal chromosome 18q deletion syndrome', 'deletion 18q', 'partial deletion of chromosome 18q']",0060407,601808,262146,C0432443,,C84522,,C536580,758.39,,,
mondo:0011148,Spondylospinal thoracic dysostosis,['spondylospinal thoracic dysostosis'],,601809,,C1866184,,,,C566622,,,,
mondo:0011149,"premature aging syndrome, Okamoto type","['premature ageing syndrome with osteosarcoma cataracts diabetes osteoporosis erythroid macrocytosis severe developmental delay', 'premature aging syndrome with osteosarcoma cataracts diabetes osteoporosis erythroid macrocytosis severe developmental delay', 'premature ageing Okamoto type', 'premature aging syndrome, Okamoto type', 'premature aging Okamoto type']",,601811,,C1866183,,,,C566621,,,,
mondo:0011150,acroosteolysis-keloid-like lesions-premature aging syndrome,"['progeroid syndrome, Penttinen type', 'premature ageing syndrome, Penttinen type', 'premature ageing syndrome Penttinen type', 'premature aging syndrome Penttinen type', 'PENTT', 'premature aging syndrome, Penttinen type', 'Penttinen-aula syndrome', 'prematurely aged appearance, delayed bone maturation, acro-osteolysis, and brachydactyly']",,601812,363665,C1866182,"['-0.68', '-0.258', '0.1475', '-0.1661', '0.4631', '-0.4958', '-0.3604', '0.6455', '-0.8374', '0.3088', '-0.244', '-0.143', '0.1663', '-0.2778', '-0.369', '0.00812', '0.6157', '-0.0885', '-0.1647', '-0.6006', '0.02464', '-0.277', '0.1644', '0.03503', '0.5786', '0.113', '-0.2141', '0.1732', '0.3486', '-0.379', '0.3625', '-0.1742', '0.556', '0.01608', '0.3044', '0.05795', '-0.10065', '-0.1943', '0.4397', '-0.8984', '0.1877', '-0.2505', '-0.2312', '0.1421', '0.3403', '-0.4404', '0.2268', '0.7715', '0.299', '-0.3564', '-0.1345', '0.1622', '-0.001781', '0.55', '-0.4885', '-0.6084', '-0.1602', '0.09216', '-0.1947', '-0.0462', '-0.04633', '0.0864', '-0.445', '-0.06793', '-0.1693', '0.04596', '0.1659', '0.7485', '0.155', '0.4495', '-0.7627', '-0.1197', '0.455', '0.0157', '-0.3442', '0.04483', '-0.0498', '0.1299', '-0.294', '-0.1711', '0.08203', '-0.3804', '0.01013', '0.3167', '-0.0952', '-0.05408', '0.0453', '0.549', '0.5303', '0.274', '-0.3079', '0.2183', '0.196', '0.4463', '0.3035', '-0.11914', '0.64', '0.0001382', '0.4634', '0.07056']",,,C536653,,,,
mondo:0011151,exudative vitreoretinopathy 4,"['EVR4', 'exudative vitreoretinopathy 4', 'exudative vitreoretinopathy type 4']",0111411,601813,,C1866176,,,,C566619,,,,
mondo:0011152,PHGDH deficiency,"['PHGDH deficiency', '3-phosphoglycerate dehydrogenase deficiency, infantile/juvenile form', 'PHGDHD', 'PHOSPHOGLYCERATE dehydrogenase deficiency']",0050722,601815,79351,C1866174,"['-0.4573', '0.4497', '0.2455', '-0.1794', '-0.0157', '-0.3657', '-0.2107', '0.2603', '-0.2158', '-0.375', '-0.3', '-0.1561', '-0.2134', '-0.4521', '0.00813', '-0.01779', '0.23', '-0.09705', '-0.2632', '-0.748', '0.02443', '-0.072', '0.1774', '-0.456', '0.0933', '0.1032', '-0.2335', '-0.2468', '0.178', '-0.2817', '-0.06415', '0.333', '0.4075', '0.3606', '-0.2026', '0.1093', '-0.3003', '-0.3071', '-0.3994', '-0.0714', '0.3152', '-0.7827', '0.11835', '-0.2766', '-0.117', '-0.1249', '0.1138', '0.2188', '0.1951', '0.3652', '-0.006638', '-0.006813', '-0.3354', '-0.00631', '-0.1569', '-0.3796', '0.1244', '-0.04102', '-0.5527', '0.5967', '0.2015', '-0.2566', '0.5186', '-0.1326', '0.1287', '-0.1255', '0.1941', '-0.1599', '-0.571', '0.0624', '-0.1482', '0.0701', '0.10657', '-0.1959', '0.1063', '0.3398', '0.4177', '-0.3716', '-0.3738', '0.2524', '0.4407', '0.1159', '-0.2593', '0.10706', '0.6475', '0.163', '0.187', '0.306', '0.573', '0.2705', '0.2279', '0.7764', '0.07733', '-0.00938', '0.4758', '0.7036', '0.3843', '-0.5215', '0.3464', '0.06073']",,,C566618,,,,
mondo:0011153,"hyperinsulinemic hypoglycemia, familial, 2","['hyperinsulinemic hypoglycemia due to Kir6.2 deficiency', 'HHF2', 'persistent hyperinsulinemic hypoglycemia of infancy', 'hyperinsulinism, congenital', 'nesidioblastosis', 'hyperinsulinemic hypoglycemia familial 2', 'hyperinsulinism, neonatal', 'KCNJ11 hyperinsulinemic hypoglycemia (disease)', 'hyperinsulinism, familial', 'hyperinsulinemic hypoglycemia, persistent', 'hyperinsulinemic hypoglycemia, familial, type 2', 'hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia', 'hyperinsulinemic hypoglycemia, familial, 2']",0070218,601820,,C2931833,"['-0.04724', '0.06805', '0.00285', '-0.01322', '0.007423', '-0.07855', '0.01627', '0.0793', '-0.0593', '-0.00501', '-0.02817', '-0.012825', '-0.01207', '0.01551', '-0.05225', '-0.0693', '-0.01493', '-0.02055', '-0.00832', '-0.137', '0.002707', '-0.0344', '0.04526', '-0.02301', '0.003721', '-0.01814', '-0.00648', '-0.03412', '-0.001547', '-0.04193', '0.0779', '0.00774', '0.09106', '0.02948', '-0.005127', '-0.013855', '-0.01349', '-0.00984', '-0.02943', '-0.05753', '0.03302', '-0.0767', '0.04654', '-0.002724', '-0.004814', '-0.05197', '-0.01418', '0.05225', '0.00459', '0.05548', '-0.02989', '-0.01109', '0.0326', '0.01269', '-0.04626', '-0.02097', '0.05194', '-0.0464', '-0.0807', '0.01242', '0.03848', '0.0562', '0.03564', '-0.03342', '-0.002918', '0.01778', '0.0953', '0.0563', '-0.08527', '0.0753', '-0.0427', '0.02255', '0.01427', '-0.077', '0.0437', '0.04025', '0.03174', '0.01445', '-0.05548', '-0.0468', '-0.00316', '0.024', '-0.02711', '0.008514', '0.01599', '0.02437', '0.02635', '0.05286', '0.1081', '0.009415', '0.03073', '0.066', '0.01923', '-0.00596', '0.155', '0.03836', '0.0637', '-0.1193', '-0.0281', '0.0292']",,,,,,,
mondo:0011154,"acrofacial dysostosis, Palagonia type","['acrofacial dysostosis, Palagonia type', 'Palagonia type of acrofacial dysostosis', 'Palagonia form of AFD', 'AFD- Palagonia type', 'acrofacial dysostosis Palagonia type', 'PAFD', 'acrofacial dysostosis, Patagonia type']",0060385,601829,1787,C1866168,,,,C538185,,,,
mondo:0011155,vacuolar Neuromyopathy,"['vacuolar Neuromyopathy', 'muscular dystrophy, autosomal dominant, with rimmed vacuoles', 'muscular dystrophy with rimmed vacuoles']",,601846,,C1866139,,,,C566617,,,,
mondo:0011156,progressive familial intrahepatic cholestasis type 2,"['severe ABCB11 deficiency', 'progressive familial intrahepatic cholestasis caused by mutation in ABCB11', 'cholestasis, progressive familial intrahepatic, 2', 'cholestasis, progressive familial intrahepatic 2', 'PFIC2', 'BSEP deficiency', 'ABCB11 progressive familial intrahepatic cholestasis', 'cholestasis, progressive familial intrahepatic, type 2']",0070222,601847,79304,CN205889,"['0.459', '0.3079', '-0.141', '0.1276', '-0.2612', '-0.4434', '-0.00599', '0.781', '-0.1334', '0.2394', '-0.1231', '-0.2979', '-0.4043', '0.2032', '-0.604', '-0.264', '0.3477', '-0.319', '0.4644', '-0.888', '-0.309', '-0.3054', '0.9414', '-0.2472', '-0.03223', '0.06714', '-0.11615', '0.4458', '-0.3303', '-0.4424', '0.882', '0.001477', '0.2874', '0.3108', '-0.661', '-0.455', '-0.2212', '0.12103', '0.01485', '0.2852', '-0.1034', '-0.118', '0.5303', '0.36', '-0.1969', '0.07245', '0.01521', '-0.2478', '-0.1528', '-0.502', '0.01996', '0.2966', '0.305', '-0.69', '-0.05295', '-0.1567', '0.3494', '0.2041', '-0.2559', '0.4294', '0.793', '-0.2156', '0.518', '-0.00401', '0.5864', '-0.1703', '0.845', '0.4055', '-0.1486', '0.603', '0.2961', '0.0179', '0.1912', '-0.4548', '0.7007', '0.2301', '-0.2803', '-0.1143', '-0.3745', '-0.1614', '-0.17', '-0.2352', '-1.038', '-0.2605', '-0.7793', '-0.1307', '0.2883', '-0.1436', '0.6733', '-0.10376', '0.702', '0.1766', '-0.33', '0.3276', '0.58', '-0.1499', '0.2812', '-0.3796', '-0.00577', '-0.2812']",,,,,,,
mondo:0011157,Gomez-Lopez-Hernandez syndrome,"['Gomez Lopez Hernandez syndrome', 'craniosynostosis-alopecia-brain defect syndrome', 'Gomez-Lopez-Hernandez syndrome', 'Cerebellotrigeminal dermal dysplasia', 'GLHS', 'Gomez-Lopez-Hernández syndrome', 'Gómez-López-Hernández syndrome', 'Cerebellotrigeminal dermal dysplasia cerebello-trigeminal-dermal dysplasia', 'Cerebellotrigeminal-dermal dysplasia', 'Cerebellotrigeminal-dermal dysplasia syndrome', 'GOMEZ-LOPEZ-HERNANDEZ syndrome']",,601853,1532,,,,,C537285,,,,
mondo:0011158,autoimmune lymphoproliferative syndrome type 1,"['autoimmune lymphoproliferative syndrome, type IA', 'autoimmune lymphoproliferative syndrome, type 1A', 'autoimmune lymphoproliferative syndrome, type I, autosomal recessive', 'autoimmune lymphoproliferative syndrome, type IB', 'autoimmune lymphoproliferative syndrome', 'autoimmune lymphoproliferative syndrome, type 1B', 'autoimmune lymphoproliferative syndrome, type I, autosomal dominant', 'ALPS', 'Canale-Smith syndrome']",,601859,,,,,,,279.41,,,
mondo:0011159,autosomal dominant nonsyndromic hearing loss 13,"['autosomal dominant deafness 13', 'deafness, autosomal dominant 13', 'deafness, autosomal dominant type 13', 'autosomal dominant nonsyndromic deafness 13', 'DFNA13', 'COL11A2 autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness type 13', 'autosomal dominant nonsyndromic deafness caused by mutation in COL11A2']",0110545,601868,,C1866095,,,,C566612,,,,
mondo:0011160,autosomal recessive nonsyndromic hearing loss 15,"['deafness, autosomal recessive type 15', 'autosomal recessive deafness 72', 'autosomal recessive deafness 95', 'autosomal recessive nonsyndromic deafness 15', 'DFNB15', 'autosomal recessive nonsyndromic deafness type 15', 'DFNB95', 'autosomal recessive nonsyndromic deafness caused by mutation in GIPC3', 'deafness, autosomal recessive 72', 'DFNB72', 'autosomal recessive deafness 15', 'GIPC3 autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive 95', 'deafness, autosomal recessive 15']",0110470,601869,,C1866094,,,,C566611,,,,
mondo:0011161,sperm-specific antigen 1,"['fertilization antigen 1', 'SSFA1', 'sperm-specific antigen 1', 'fertilisation antigen 1', 'sperm-specific antigen type 1']",,601876,,,,,,,,,,
mondo:0011162,cataract 14 multiple types,"['cataract, zonular pulverulent 3', 'GJA3 early-onset non-syndromic cataract', 'cataract 14, multiple types', 'Cae3', 'CAE3', 'CZP3', 'zonular pulverulent cataract 3', 'early-onset non-syndromic cataract caused by mutation in GJA3', 'CTRCT14']",0110253,601885,98993,C1866078,,,,C566608,,,,
mondo:0011163,"malignant hyperthermia, susceptibility to, 5","['CACNA1S malignant hyperthermia of anaesthesia', 'Mhs5', 'malignant hyperthermia of anaesthesia caused by mutation in CACNA1S', 'malignant hyperthermia susceptibility 5', 'malignant hyperthermia of anesthesia caused by mutation in CACNA1S', 'malignant hyperthermia, susceptibility to, 5', 'malignant hyperthermia, susceptibility to, type 5', 'CACNA1S malignant hyperthermia of anesthesia', 'MHS5', 'susceptibility to malignant hyperthermia 5', 'malignant hyperpyrexia susceptibility type 5', 'malignant hyperthermia susceptibility type 5']",,601887,,,"['-0.04037', '0.04364', '-0.006706', '-0.02518', '0.02219', '-0.081', '0.04382', '0.06683', '-0.03934', '-0.0539', '-0.01836', '0.02759', '-0.0043', '0.006733', '-0.0335', '-0.03766', '-0.005802', '-0.05988', '-0.02295', '-0.1085', '0.002073', '-0.0353', '0.07043', '-0.011665', '-0.01038', '-0.02803', '-0.01122', '0.00577', '-0.01279', '-0.06128', '0.05447', '-0.00784', '0.05402', '0.00743', '-0.003616', '-0.0318', '-0.03574', '-0.04343', '-0.02116', '-0.05505', '0.0329', '-0.03467', '0.04263', '-0.01384', '-0.013725', '-0.04556', '-0.02017', '0.0285', '0.004288', '0.04544', '-0.02557', '-0.00941', '0.01463', '0.02547', '-0.01895', '-0.024', '0.04456', '-0.01903', '-0.04535', '-0.01246', '0.05243', '0.02568', '-0.001625', '0.0176', '0.00816', '0.02806', '0.0662', '0.0629', '-0.05948', '0.0749', '-0.01843', '0.001115', '0.01269', '-0.0657', '0.04303', '0.04153', '-0.006577', '-0.00988', '-0.02962', '-0.02988', '-0.006065', '-0.00168', '-0.00442', '0.0487', '-0.03696', '0.0001079', '0.0374', '0.04144', '0.0623', '-0.0191', '0.04407', '0.03885', '-0.01455', '0.0185', '0.1271', '0.04263', '0.04156', '-0.07544', '-0.03017', '0.009544']",,,C535698,,,,
mondo:0011164,"malignant hyperthermia, susceptibility to, 6","['malignant hyperthermia susceptibility type 6', 'MHS6', 'malignant hyperthermia susceptibility 6', 'malignant hyperthermia, susceptibility to, 6', 'malignant hyperpyrexia susceptibility type 6', 'Mhs6', 'malignant hyperthermia, susceptibility to, type 6']",,601888,,,,,,C535699,,,,
mondo:0011165,glomerulopathy with fibronectin deposits 2,"['GFND2', 'glomerular nephritis familial with fibronectin deposits', 'fibronectin glomerulopathy', 'glomerulopathy with fibronectin deposits type 2', 'glomerular nephritis, familial, with fibronectin deposits', 'FN1 fibronectin glomerulopathy', 'glomerulopathy with fibronectin deposits 2', 'fibronectin glomerulopathy caused by mutation in FN1']",,601894,,,,,,,,,,
mondo:0011166,lymphedema-atrial septal defects-facial changes syndrome,"['Irons Bhan syndrome', 'lymphedema, atrial septal defect, and characteristic facies', 'Irons-Bhan syndrome', 'lymphedema, atrial septal defect, and characteristic facial changes', 'Irons-Bianchi syndrome', 'lymphedema, CARDIAC septal defects, and characteristic facies', 'autosomal recessive syndrome of lymphedema, hydroceles, atrial septal defect, and characteristic facial changes']",,601927,86915,,,,,C567398,,,,
mondo:0011167,type 1 diabetes mellitus 6,"['autoimmune thyroid disease, susceptibility to, 5', 'IDDM6', 'insulin-dependent diabetes mellitus 6', 'diabetes mellitus, insulin-dependent, 6']",0110745,601941,,C1866041,,,,C566603,,,,
mondo:0011168,type 1 diabetes mellitus 10,"['diabetes, mellitus, insulin-dependent, susceptibility to, 10', 'IDDM10', 'type 1 diabetes mellitus caused by mutation in IL2RA', 'diabetes mellitus, insulin-dependent, 10', 'insulin-dependent diabetes mellitus 10', 'IL2RA type 1 diabetes mellitus', 'diabetes mellitus, insulin-dependent, type 10']",0110749,601942,,C1866040,,,,C566602,,,,
mondo:0011169,keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome,"['Klick syndrome', 'KLICK', 'keratosis linearis with ichthyosis congenita and sclerosing keratoderma', 'KLICK syndrome']",,601952,281201,C1866029,"['-0.3083', '0.3008', '0.03506', '-0.511', '0.4207', '-0.9624', '-0.7866', '0.1268', '-1.018', '-0.0001982', '0.2197', '0.4863', '0.08215', '0.1484', '-0.34', '0.4524', '0.5', '-0.5996', '0.1731', '-1.194', '0.06525', '0.0467', '0.4915', '-0.207', '0.1703', '0.5093', '-0.2212', '0.4626', '0.1643', '-0.1935', '0.3245', '-0.291', '-0.02167', '0.4495', '0.216', '0.00931', '0.1145', '-0.3', '0.1542', '-0.2837', '0.01115', '-0.609', '-0.293', '0.1691', '0.1608', '0.05057', '-0.2311', '0.5254', '0.619', '-0.154', '-0.4504', '0.0468', '0.10803', '0.1715', '-0.6387', '-0.2339', '0.7275', '0.3254', '-0.628', '-0.2993', '0.08984', '-0.00745', '-0.6323', '0.04486', '0.1838', '0.2847', '0.4604', '0.525', '-0.002895', '0.439', '-0.4966', '-0.085', '0.1283', '-0.02798', '-0.0593', '0.5415', '0.01869', '-0.0521', '-0.09607', '-0.659', '-0.2482', '-0.2065', '-0.0401', '-0.04373', '0.01671', '-0.2153', '-0.3271', '0.4944', '0.413', '0.3325', '-0.01166', '0.02855', '0.5034', '-0.00994', '0.211', '-0.09326', '0.652', '-0.506', '0.431', '-0.1277']",,,C566600,,,,
mondo:0011170,autosomal recessive limb-girdle muscular dystrophy type 2G,"['Tcap autosomal recessive limb-girdle muscular dystrophy', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in Tcap', 'limb-girdle muscular dystrophy, type 2G', 'LGMD2G', 'muscular dystrophy, limb-girdle, type 2G', 'TCAP autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, limb-girdle, autosomal recessive 7', 'limb-girdle muscular dystrophy due to telethonin deficiency']",0110281,601954,34514,,"['-0.0744', '-0.6704', '-0.7124', '-0.1908', '0.565', '-1.262', '0.2191', '0.7617', '-1.8545', '-0.8135', '0.2925', '0.364', '-0.4507', '1.022', '0.1718', '0.4329', '-0.7534', '-0.3657', '-0.6426', '-0.841', '-0.1488', '0.1175', '0.483', '0.7266', '0.2206', '0.1218', '-0.08655', '-0.7236', '0.3684', '-0.5933', '0.9473', '0.08466', '0.556', '0.1299', '0.1266', '-0.05527', '-0.783', '0.3425', '0.1705', '-0.4238', '0.2125', '-0.407', '-0.6567', '0.4438', '-0.429', '0.358', '-0.0621', '0.6914', '-0.1372', '0.6113', '0.3418', '-0.4697', '0.185', '-0.8955', '0.06744', '-0.752', '0.3757', '0.7803', '-0.1953', '-0.0111', '-0.07886', '0.1824', '0.03586', '0.1305', '-0.1805', '0.1737', '0.2377', '0.634', '-0.35', '-0.381', '-0.2878', '0.59', '0.1887', '0.1222', '0.539', '0.8193', '-0.01155', '0.3105', '0.041', '0.01236', '-0.1242', '0.001035', '-0.0587', '0.1682', '0.10474', '0.2328', '-0.2893', '-0.3713', '1.069', '0.2388', '-0.3115', '0.1798', '0.264', '0.847', '0.0359', '0.0004494', '0.2051', '-0.2605', '0.05682', '-0.0483']",,,C566599,,,,
mondo:0011171,odonto-tricho-ungual-digito-palmar syndrome,"['odonto-tricho-ungual-digito-palmar syndrome, Mendoza-Valiente type', 'ODONTOTRICHOUNGUAL-digital-palmar syndrome', 'OTUDP syndrome', 'Otudp syndrome']",,601957,69082,C1865998,,,,C566598,,,,
mondo:0011172,otofacioosseous-gonadal syndrome,['otofacioosseous-gonadal syndrome'],,601976,,C1865988,,,,C566597,,,,
mondo:0011173,thrombocythemia 2,"['thrombocythemia 2', 'thrombocythemia type 2', 'MPL familial thrombocytosis', 'THCYT2', 'familial thrombocytosis caused by mutation in MPL', 'thrombocythemia 2, autosomal dominant, somatic mutation']",,601977,71493,C3275998,,,,,,,,
mondo:0011174,hyperzincemia with functional zinc depletion,['hyperzincemia with functional zinc depletion'],,601979,,C1865986,,,,C566595,,,,
mondo:0011175,Friedreich ataxia 2,"['FRDA2', 'Friedreich ataxia 2']",0111219,601992,,C1865981,,,,C566594,,,,
mondo:0011176,intestinal hypomagnesemia 1,"['intestinal hypomagnesemia type 1', 'hypomagnesemia 1, intestinal', 'hypomagnesemia, intestinal, with secondary hypocalcemia', 'primary hypomagnesemia caused by mutation in TRPM6', 'hypomagnesemia intestinal type 1', 'HSH', 'hypomagnesemia caused by selective magnesium malabsorption', 'TRPM6 familial primary hypomagnesemia', 'hypomagnesemic tetany', 'TRPM6 primary hypomagnesemia', 'HOMG1', 'PHSH', 'intestinal hypomagnesemia with secondary hypocalcemia', 'Homg', 'primary hypomagnesemia with secondary hypocalcemia', 'hypomagnesemia with secondary hypocalcemia']",0060883,602014,30924,C1865974,"['0.1333', '0.012596', '-0.3865', '-0.3274', '-0.295', '-0.235', '0.0772', '0.394', '-0.691', '-0.11316', '-1.086', '-0.3613', '-0.3564', '0.714', '-0.4058', '0.3376', '0.00546', '-0.4604', '-0.09467', '-1.624', '-0.3252', '-0.2301', '0.606', '-0.385', '-0.0679', '0.06464', '-0.11346', '0.09686', '-0.2493', '-0.08386', '0.3184', '0.301', '0.6836', '0.0664', '-0.2491', '0.0584', '0.257', '-0.2727', '-0.4666', '0.433', '-0.04858', '-0.3013', '0.567', '-0.2612', '0.6807', '0.0867', '-0.539', '-0.03427', '-0.295', '0.7466', '-0.004765', '0.0894', '0.9272', '-0.1239', '-0.4128', '-0.09784', '0.385', '-0.235', '0.1006', '0.495', '0.1709', '0.1794', '-0.03284', '-0.3228', '-0.295', '-0.05563', '0.577', '0.254', '0.0663', '-0.1321', '0.3455', '0.1337', '0.3665', '-0.2252', '0.1183', '0.1935', '0.3906', '-0.3518', '0.0819', '0.0317', '0.687', '0.4753', '0.0876', '-0.2048', '0.4026', '0.012146', '0.1947', '-0.0706', '0.3342', '0.1584', '0.4746', '-0.1669', '0.07404', '-0.2133', '0.3997', '0.6846', '0.695', '-0.1771', '-0.0978', '0.07666']",,,C566593,,,,
mondo:0011177,"ectodermal dysplasia 4, hair/nail type","['pure hair and nail ectodermal dysplasia caused by mutation in KRT85', 'pili torti onychodysplasia', 'ECTD4', 'ectodermal dysplasia, ^Pure^ hair/nail type', 'twisted hair with nail dysplasias', 'ectodermal dysplasia 4, hair/nail type', 'KRT85 pure hair and nail ectodermal dysplasia']",0111658,602032,,C2931483,,,,C566592,,,,
mondo:0011178,infantile convulsions and choreoathetosis,"['convulsions, familial infantile, with paroxysmal choreoathetosis', 'ICCA', 'PKD/IC', 'convulsions, infantile, with paroxysmal choreoathetosis, familial', 'ICCA syndrome', 'infantile convulsions and paroxysmal choreoathetosis, familial', 'paroxysmal kinesigenic dyskinesia with infantile convulsions', 'paroxysmal kinesigenic dyskinesia and infantile convulsions', 'Icca syndrome']",,602066,31709,C1865926,"['0.3354', '0.6396', '-0.5757', '-0.2578', '-0.639', '-1.013', '0.5083', '0.559', '-0.5435', '-0.656', '-0.2474', '-0.02301', '0.05118', '0.03177', '0.4062', '0.2524', '-0.1584', '-0.5493', '0.359', '-0.63', '0.2563', '-0.1324', '0.516', '-0.8823', '-0.2585', '-0.04916', '0.08325', '-0.1702', '-0.5195', '-0.2725', '0.733', '0.3103', '-0.0994', '0.3716', '-0.4238', '0.3242', '-0.2126', '8.935e-05', '-0.7993', '0.10565', '0.676', '-0.3196', '0.226', '0.4045', '0.3616', '0.2676', '-0.456', '0.0852', '-0.1776', '0.9595', '-0.1631', '0.8027', '0.0825', '-0.1866', '0.6123', '-0.1852', '0.3855', '-0.318', '-0.511', '0.3845', '-0.3887', '0.3694', '0.922', '0.2247', '-0.147', '0.2135', '0.99', '-0.172', '-0.813', '0.5845', '0.605', '-0.03033', '0.08704', '-0.1091', '0.1194', '0.734', '-0.0666', '0.547', '-0.3613', '0.2622', '0.2961', '0.707', '0.394', '0.0856', '0.1497', '-0.579', '0.3123', '0.5654', '0.278', '0.6455', '0.2822', '0.3994', '0.2316', '-0.2764', '0.569', '0.03018', '0.6104', '-0.629', '-0.2175', '0.1004']",C126650,,C535522,,,,
mondo:0011179,"leishmaniasis, tegumentary, susceptibility to","['leishmaniasis, tegumentary, susceptibility to']",,602068,,,,,,,,,,
mondo:0011180,"broad terminal phalanges, familial","['broad terminal phalanges, familial']",,602071,,C1865923,,,,C566588,,,,
mondo:0011181,"fibrosis of extraocular muscles, congenital, 2","['fibrosis of extraocular muscles, congenital, autosomal recessive', 'fibrosis of extraocular muscles, congenital, type 2', 'CFEOM2', 'PHOX2A congenital fibrosis of extraocular muscles', 'Feom2 locus', 'congenital fibrosis of extraocular muscles caused by mutation in PHOX2A', 'fibrosis of extraocular muscles, congenital, 2']",0081016,602078,,C1865915,,,,C566587,,,,
mondo:0011182,trimethylaminuria,"['trimethylaminuria', 'fish odour syndrome', 'fish malodor syndrome', 'fish odor syndrome', 'TMAU', 'trimethylaminuria (disease)', 'TMAuria', 'stale fish syndrome', 'fish-odor syndrome']",,,35056,C0342739,,,,,,,,0003614
mondo:0011183,"Paget disease of bone 2, early-onset","['PDB2', 'Paget disease of bone 2, early-onset']",0081365,602080,,C4085251,,,,,,,,
mondo:0011184,childhood apraxia of speech,"['das', 'articulatory apraxia', 'speech-language disorder-1', 'SPCH1', 'speech-language disorder type 1', 'developmental verbal apraxia', 'developmental verbal dyspraxia', 'CAS', 'childhood apraxia of speech', 'speech and language disorder with orofacial dyspraxia', 'developmental apraxia of speech', 'speech-language disorder 1']",0111275,602081,209908,,"['0.5586', '-0.2401', '0.1929', '0.4214', '-0.2842', '-0.01015', '-0.06555', '0.329', '-0.5635', '-0.3594', '0.4631', '0.1731', '-0.04477', '0.3508', '0.992', '-0.2737', '-0.04657', '-0.54', '-0.4329', '-0.9766', '-0.1394', '0.454', '-0.4834', '0.2457', '0.2024', '-0.3794', '-0.5723', '-0.10895', '-0.0947', '-0.05737', '0.0867', '-0.4736', '0.4854', '1.011', '0.3132', '0.2046', '-0.2476', '0.375', '-0.242', '-1.082', '0.384', '-0.0299', '-0.54', '0.1277', '0.853', '-0.539', '0.1232', '-0.218', '-0.05255', '-0.2167', '0.03094', '0.178', '-0.7456', '0.02199', '0.6743', '0.1698', '-0.4048', '0.567', '-0.1309', '0.2908', '-0.1525', '0.662', '0.6235', '0.1493', '-0.479', '-0.292', '0.5654', '0.0673', '0.04517', '0.4463', '0.0908', '-0.1613', '0.07056', '-0.494', '0.5806', '0.549', '0.1804', '0.4717', '-0.2583', '-0.794', '0.5894', '-0.2225', '0.2644', '0.2443', '-0.2394', '0.06116', '-0.02309', '0.512', '1.29', '0.08777', '-0.3367', '0.1636', '-0.7017', '0.3438', '0.4395', '0.7393', '-0.2761', '-0.7056', '0.1875', '0.2097']",,,,315.39,,,
mondo:0011185,Thiel-Behnke corneal dystrophy,"['anterior limiting membrane dystrophy type II', 'corneal dystrophy honeycomb shaped', 'anterior limiting membrane dystrophy type 2', 'Waardenburg-Jonker corneal dystrophy', 'corneal dystrophy, honeycomb-Shaped', 'curly fibre corneal dystrophy', 'corneal dystrophy of the Bowman layer type 2', 'Thiel Behnke corneal dystrophy', 'corneal dystrophy of Bowman layer type II', 'Thiel-Behnke corneal dystrophy', 'honeycomb corneal dystrophy', 'corneal dystrophy, Thiel-Behnke type', 'curly fiber corneal dystrophy', 'CDTB', 'corneal dystrophy of Bowman Layer, type 2', 'corneal dystrophy of Bowman layer type 2', 'CDB2', 'TBCD', 'corneal dystrophy Thiel Behnke type', 'corneal dystrophy honeycomb-shaped']",0060455,602082,98960,C1562894,"['-0.5205', '-0.267', '-0.5845', '0.1411', '0.3303', '-0.61', '-0.1967', '0.3142', '-0.2489', '-0.3057', '-0.09894', '-0.4143', '-0.1488', '0.3586', '-0.3923', '-0.2593', '0.2035', '-0.499', '-0.1929', '-0.545', '-0.3044', '-0.0273', '-0.01458', '0.2556', '-0.08356', '0.341', '-0.3672', '0.0883', '-0.6104', '0.227', '0.6597', '-0.03062', '-0.0223', '-0.0241', '0.2064', '0.2029', '-0.006577', '-0.4028', '0.2245', '-0.1632', '0.306', '-0.486', '0.281', '0.155', '-0.1925', '0.6626', '-0.0355', '-0.2764', '-0.03134', '0.3079', '0.5376', '0.2883', '0.5312', '-0.09784', '0.0634', '0.1399', '0.4004', '0.3374', '-0.8506', '-0.10394', '0.443', '-0.474', '0.03778', '0.158', '0.11273', '-0.11743', '0.4604', '0.7075', '-0.02145', '0.516', '-0.375', '-0.4236', '0.08167', '-0.2294', '0.5', '0.3318', '-0.012184', '0.2576', '-0.04904', '0.05777', '-0.06885', '-0.1765', '-0.2295', '0.4998', '-0.10236', '-0.641', '-0.307', '0.3381', '0.010506', '-0.01321', '-0.03867', '0.2595', '-0.09393', '0.2593', '0.458', '0.02544', '0.477', '-0.546', '-0.05515', '0.287']",,,C535942,371.52,,,
mondo:0011186,Usher syndrome type 1F,"['Usher syndrome type IF', 'Usher syndrome, type 1F', 'USHER syndrome, type IF', 'USH1F']",0110832,602083,,C1865885,,,,,,H35.5,,
mondo:0011187,"polydactyly, postaxial, type A2","['PAPA2', 'polydactyly, postaxial, type A2', 'postaxial polydactyly, type A2']",,602085,,C1865883,,,,C566585,,,,
mondo:0011188,arrhythmogenic right ventricular dysplasia 3,"['ARVD3', 'ARVC3', 'familial arrhythmogenic right ventricular dysplasia 3', 'arrhythmogenic right ventricular cardiomyopathy 3', 'arrhythmogenic right ventricular dysplasia type 3', 'arrhythmogenic right ventricular dysplasia, familial, 3']",0110072,602086,,C1865882,,,,C566584,,,,
mondo:0011189,arrhythmogenic right ventricular dysplasia 4,"['ARVD4', 'arrhythmogenic right ventricular cardiomyopathy 4', 'arrhythmogenic right ventricular dysplasia type 4', 'fanilial arrhythmogenic right ventricular dysplasia 4', 'ARVC4', 'arrhythmogenic right ventricular dysplasia, familial, 4']",0110073,602087,,C1865881,,,,C566583,,,,
mondo:0011190,nephronophthisis 2,"['NPHP2', 'INVS nephronophthisis (disease)', 'nephronophthisis 2', 'nephronophthisis 2, infantile', 'nephronophthisis type 2', 'NPH2', 'Nph2', 'infantile nephronophthisis 2']",0111113,602088,93591,C1865872,"['-0.05426', '-0.1001', '0.1948', '0.2874', '0.1982', '-0.3066', '-0.1665', '0.755', '-0.926', '-0.01359', '-0.1462', '-0.507', '-0.1877', '0.4636', '0.03622', '-0.1829', '0.3538', '0.338', '-0.1346', '-0.4194', '-0.07495', '-0.1608', '0.7007', '-0.0522', '0.2607', '-0.2861', '0.186', '0.639', '0.262', '0.2231', '0.3777', '-0.01385', '0.699', '0.1042', '0.231', '-0.01872', '-0.11475', '0.1553', '0.3738', '0.3225', '-0.2551', '-0.4258', '0.5806', '-0.05844', '0.2319', '-0.0841', '-0.0637', '-0.08734', '-0.2954', '-0.1197', '-0.306', '-0.2311', '0.1792', '-0.362', '-0.1156', '-0.306', '-0.4148', '0.02089', '-0.7334', '-0.3455', '0.2825', '-0.11444', '0.1112', '-0.1542', '0.2303', '-0.78', '0.9565', '-0.1484', '-0.799', '-0.1586', '-0.148', '-0.221', '0.02359', '-0.0535', '0.2142', '-0.803', '0.398', '-0.0712', '-0.3936', '0.307', '0.02061', '0.002497', '0.1635', '-0.03192', '-0.411', '-0.1523', '0.4043', '-0.1907', '0.365', '0.04254', '0.1031', '0.2766', '-0.1271', '-0.4785', '0.761', '0.088', '0.759', '-0.0799', '-0.3826', '0.3667']",,,C566582,,,,
mondo:0011191,capillary infantile hemangioma,"['hemangioma, capillary infantile, somatic', 'hemangioma, capillary infantile', 'hereditary capillary infantile hemangioma', 'HCI', 'hemangioma, hereditary capillary']",,602089,91415,C1865871,"['-0.3066', '0.0919', '-0.4575', '0.2566', '0.1991', '-0.5176', '-0.2534', '0.569', '-0.8247', '-0.11884', '0.1771', '0.2542', '0.05356', '0.1029', '-0.257', '-0.343', '-0.3247', '-0.45', '0.3425', '-0.568', '-0.2832', '0.2201', '0.2795', '-0.2852', '0.2043', '-0.1171', '-0.5903', '0.4243', '-0.09814', '0.568', '-0.1426', '-0.3325', '-0.1162', '-0.09546', '0.0739', '1.165', '-0.3845', '0.2502', '0.3289', '-0.2842', '0.4434', '0.3179', '-0.3293', '-0.4983', '0.04596', '0.07007', '-0.9053', '0.3875', '0.3284', '-0.308', '0.10364', '0.03848', '0.698', '0.1873', '-0.3362', '-0.0952', '-0.03093', '0.2512', '-0.1626', '-0.04453', '-0.07184', '0.3005', '-0.0627', '0.2144', '-0.196', '0.08014', '0.9946', '0.463', '-0.7446', '0.9663', '0.2827', '0.4084', '0.2225', '-0.269', '-0.15', '0.2145', '-0.1514', '0.645', '-0.0315', '-0.1355', '-0.5117', '0.1074', '-0.4614', '0.12463', '0.1954', '-0.0986', '0.1456', '-0.005466', '0.2157', '0.4678', '0.4583', '-0.05045', '0.2477', '0.5635', '0.4382', '-0.0968', '-0.4382', '-0.7207', '-0.02797', '0.1197']",,,C535860,,,,
mondo:0011192,autosomal recessive nonsyndromic hearing loss 18A,"['autosomal recessive nonsyndromic deafness 18A', 'deafness, autosomal recessive type 18A', 'deafness, autosomal recessive 18', 'deafness, autosomal recessive 18a', 'deafness, autosomal recessive 18A', 'USH1C autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness caused by mutation in USH1C', 'DFNB18A', 'autosomal recessive nonsyndromic deafness type 18A', 'autosomal recessive deafness 18A']",0110473,602092,,C1865870,,,,C566580,,,,
mondo:0011193,cone dystrophy 3,"['COD3', 'cone-rod dystrophy 14', 'cone dystrophy-3', 'retinal cone dystrophy', 'GUCA1A cone dystrophy', 'cone dystrophy type 3', 'cone dystrophy 3', 'cone dystrophy caused by mutation in GUCA1A']",0080314,602093,,C1865869,,,,,,,,
mondo:0011194,Alzheimer disease 5,"['Alzheimer^s disease type 5', 'Ad5', 'AD5', 'Alzheimer disease-5', 'Alzheimer disease, familial, 5', 'Alzheimer disease 5', 'Alzheimer disease type 5', 'Alzheimer disease, familial 5', 'Alzheimer^s disease 5']",0110037,602096,,C1865868,,,,C566578,,,,
mondo:0011195,Usher syndrome type 1E,"['Usher syndrome, type 1E', 'USHER syndrome, type IE', 'Usher syndrome type IE', 'USH1E']",0110833,602097,,C1865865,,,,,,H35.5,,
mondo:0011196,amyotrophic lateral sclerosis type 5,"['amyotrophic lateral sclerosis caused by mutation in SPG11', 'amyotrophic lateral sclerosis 5', 'ALS5', 'SPG11 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis 5, juvenile']",0060197,602099,,C1865864,,,,C566576,,,,
mondo:0011197,hereditary thermosensitive neuropathy,"['neuropathy, hereditary thermosensitive']",,602107,84093,C1865856,,,,C566575,,,,
mondo:0011198,"spondyloepimetaphyseal dysplasia, Missouri type","['SEMD Missouri type', 'SEMD type 2', 'spondyloepimetaphyseal dysplasia, Missouri type', 'Missouri type of spondyloepimetaphyseal dysplasia', 'spondyloepimetaphyseal dysplasia Missouri type', 'spondyloepimetaphyseal dysplasia type 2', 'metaphyseal anadysplasia 1', 'SEMD, Missouri type']",0080030,602111,93356,,"['-0.5', '0.01049', '-0.151', '-0.4092', '0.2766', '-0.582', '-0.09705', '0.826', '-0.7505', '-0.865', '0.3042', '0.6587', '0.09875', '0.09265', '0.1411', '0.1643', '0.2654', '-0.02194', '-0.1064', '-0.2756', '-0.04565', '-0.03806', '0.653', '-0.1459', '0.1593', '0.1958', '0.04373', '-0.04956', '0.09973', '-0.0778', '0.479', '-0.7407', '-0.2625', '0.5244', '0.765', '-0.2266', '-0.2158', '-1.116', '0.256', '-0.2191', '0.3745', '-0.4165', '-0.2245', '0.0975', '-0.656', '0.1501', '-0.125', '0.009865', '0.04333', '-0.4993', '-0.009254', '-0.28', '-0.3938', '0.2583', '-0.05862', '-0.6177', '0.4324', '-0.2773', '-0.1434', '0.2961', '0.4778', '0.1081', '-0.574', '-0.1104', '-0.573', '0.03973', '-0.02303', '0.354', '-0.02864', '-0.05722', '-0.4905', '-0.398', '-0.2172', '-0.334', '0.0852', '0.2703', '-0.7144', '0.1235', '-0.03476', '-0.536', '-0.278', '0.4353', '0.3667', '0.5864', '0.04175', '0.2206', '0.03445', '0.5635', '0.434', '0.11237', '-0.6343', '-0.01537', '0.034', '0.0763', '0.816', '0.489', '0.8125', '-0.5176', '0.2502', '-0.1256']",,,,,,,
mondo:0011199,"nephropathy, progressive tubulointerstitial, with cholestatic liver disease","['nephropathy, progressive tubulointerstitial, with cholestatic liver disease']",,602114,,C1865831,,,,C566573,,,,
mondo:0011200,torsion dystonia 7,"['dystonia 7, torsion', 'torsion dystonia, focal adult-onset', 'cervical dystonia, primary', 'dystonia-7, torsion', 'DYT7', 'torsion dystonia type 7']",0090040,602124,93963,,,,,C566572,,,,
mondo:0011201,"tremor, hereditary essential, 2","['ETM2', 'tremor hereditary essential, 2', 'tremor, hereditary essential, 2', 'essential tremor, hereditary, 2']",0111429,602134,,,,,,C536546,,,,
mondo:0011202,RHYNS syndrome,"['RHYNS syndrome', 'retinitis pigmentosa, hypopituitarism, nephronophthisis, and mild skeletal dysplasia', 'retinitis pigmentosa syndrome', 'retinitis pigmentosa-hypopituitarism-nephronophthisis-skeletal dysplasia syndrome']",,602152,140976,C1865794,"['-0.2228', '0.3003', '0.11475', '-0.0408', '0.3633', '-0.4524', '-0.2173', '0.505', '-0.2227', '-0.532', '-0.1577', '-0.08484', '-0.2235', '-0.2069', '0.1377', '-0.10974', '-0.0628', '0.1124', '-0.564', '-0.5005', '-0.1605', '-0.04477', '0.22', '-0.1991', '0.0518', '0.186', '-0.213', '-0.1093', '0.3806', '-0.3123', '0.347', '-0.2637', '0.1011', '0.008095', '0.01593', '-0.2499', '0.08234', '-0.6553', '0.06647', '0.01323', '-0.09485', '-0.2225', '-0.168', '-0.2554', '0.1548', '-0.11456', '0.03055', '0.1788', '-0.3252', '-0.621', '0.2798', '0.15', '-0.012665', '-0.1852', '0.06903', '-0.1826', '0.4202', '0.1225', '-0.3062', '0.2275', '0.352', '-0.08844', '0.2695', '0.0912', '-0.374', '-0.0256', '0.00704', '0.534', '-0.421', '0.1343', '-0.7705', '-0.2336', '0.0824', '0.1013', '0.336', '0.1078', '-0.2096', '0.2307', '0.2124', '-0.1273', '0.2251', '0.4902', '0.05353', '0.7363', '0.02863', '0.2466', '0.3716', '0.3074', '0.1387', '0.3901', '0.09424', '0.1321', '0.2922', '-0.1418', '0.7124', '0.0462', '0.3948', '-0.859', '-0.1832', '0.02876']",,,C537612,,,,
mondo:0011203,Pierre Robin sequence with pectus excavatum and rib and scapular anomalies,"['Pierre Robin sequence with pectus excavatum and rib and scapular anomalies', 'skeletal dysplasia related to campomelic dysplasia', 'campomelic dysplasia, mild']",,602196,,C1865783,,,,C535775,,,,
mondo:0011205,medium chain 3-ketoacyl-Coa thiolase deficiency,"['Mckat deficiency', 'medium-chain 3-ketoacyl-coa thiolase deficiency', 'medium chain 3-ketoacyl-Coa thiolase deficiency']",,602199,,C1865781,,,,C566566,,,,
mondo:0011206,ventriculomegaly with defects of the radius and kidney,['ventriculomegaly with defects of the radius and kidney'],,602200,,C1865780,,,,C566565,,,,
mondo:0011207,"xanthomatosis, susceptibility to","['xanthomatosis, susceptibility to']",,602247,,C1865704,,,,,,,,
mondo:0011208,malignant atrophic papulosis,"['papulosis, malignant atrophic', 'Degos disease', 'Degos syndrome', 'Köhlmeier-Degos disease', 'malignant atrophic papulosis', 'Kohlmeier-Degos-Delort-Tricort syndrome', 'atrophic papulosis, malignant', 'Kohlmeier-Degos disease', 'papulosis atrophican maligna', 'Köhlmeier-Degos-Delort-Tricort syndrome', 'Degos^s malignant atrophic papulosis']",,602248,679,C0221011,,C84835,,D054853,447.8,,10064281,
mondo:0011209,progeroid facial appearance with hand anomalies,['progeroid facial appearance with hand anomalies'],,602249,,C1865699,,,,C566563,,,,
mondo:0011210,"mitochondrial intermembrane space protein Tim12, yeast, homolog of","['mitochondrial intermembrane space protein Tim12, yeast, homolog of']",,602252,,,,,,,,,,
mondo:0011211,axial spondylometaphyseal dysplasia,"['axial SmD', 'spondylometaphyseal dysplasia axial type', 'SmD, axial', 'spondylometaphyseal dysplasia, axial', 'SMDAX', 'SmD axial']",0112299,602271,168549,C1865695,"['-0.98', '0.1412', '0.384', '-0.455', '0.3271', '-0.7188', '-0.0635', '0.4778', '-0.788', '-0.56', '-0.3508', '0.05444', '-0.1323', '-0.1747', '-0.077', '-0.3406', '0.3594', '0.07874', '-0.1876', '-1.131', '-0.4211', '-0.2306', '0.2499', '-0.1654', '0.03745', '0.1444', '-0.2896', '-0.311', '0.06616', '0.5234', '0.2866', '-0.181', '-0.2542', '0.000396', '0.5303', '-0.05624', '0.078', '-0.2996', '0.00753', '-0.6943', '-0.4001', '-0.1544', '-0.071', '0.2527', '0.1323', '-0.2028', '-0.2386', '0.3474', '0.2754', '-0.3774', '0.826', '0.01653', '0.01866', '-0.2727', '-0.1443', '-1.23', '0.01645', '-0.0205', '-0.0891', '0.2443', '0.3125', '-0.264', '-0.613', '0.0866', '-0.1924', '-0.02661', '0.405', '0.826', '-0.2214', '0.279', '-0.2886', '-0.03638', '0.27', '-0.2244', '-0.1678', '-0.1073', '-0.3958', '0.225', '-0.04797', '-0.4814', '0.0571', '-0.1602', '-0.1053', '0.455', '-0.6616', '-0.01828', '-0.2776', '-0.0653', '0.4802', '0.1552', '0.03284', '-0.2563', '-0.4246', '0.736', '0.623', '0.231', '0.5654', '-0.2155', '0.38', '0.2532']",,,C535795,,,,
mondo:0011212,"sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth","['sensorineural hearing loss, retinal pigment epithelium lesions, discolored teeth']",,602340,,C1865645,,,,C566560,,,,
mondo:0011213,Pierpont syndrome,"['PRPTS', 'Pierpont syndrome', 'PIERPONT syndrome', 'plantar lipomatosis-facial dysmorphism-developmental delay syndrome', 'plantar lipomatosis-unusual facies-developmental delay syndrome', 'plantar lipomatosis, unusual facies, and developmental delay']",0081362,602342,487825,C1865644,"['-0.0164', '0.03918', '0.01101', '-0.00958', '0.02652', '-0.0448', '0.00436', '0.0563', '-0.04214', '-0.02011', '-0.01034', '0.00303', '-0.00678', '0.01564', '-0.005024', '-0.02115', '0.001604', '0.001134', '-0.007965', '-0.06152', '-0.000639', '-0.02039', '0.04852', '-0.02583', '0.014', '-0.009315', '-0.01973', '-0.002913', '0.02747', '-0.03696', '0.03708', '0.005775', '0.05298', '0.03482', '0.007244', '-0.01533', '-0.01547', '-0.01926', '-0.01823', '-0.0625', '0.00846', '-0.03183', '0.005516', '-0.02301', '0.01604', '-0.047', '-0.03119', '0.02213', '0.01423', '0.02263', '-0.005775', '0.00904', '-0.002178', '-0.010635', '-0.01628', '-0.01329', '0.02391', '-0.007065', '-0.04834', '0.00917', '0.04138', '-0.0002894', '0.0008063', '-0.001142', '0.005527', '-0.001403', '0.0405', '0.03247', '-0.0442', '0.05914', '-0.0579', '0.00906', '0.01274', '-0.02136', '0.01823', '0.006462', '0.002129', '0.0005836', '-0.03696', '-0.02374', '0.01348', '-0.0091', '-0.01237', '0.0397', '-0.01794', '-0.002218', '0.01826', '0.03882', '0.05823', '0.0202', '0.0219', '0.04095', '0.0009537', '0.00158', '0.0755', '0.00482', '0.04547', '-0.0669', '-0.005318', '0.01439']",,,C566559,,,,
mondo:0011214,progressive familial intrahepatic cholestasis type 3,"['cholestasis, progressive familial intrahepatic 3', 'progressive familial intrahepatic cholestasis with elevated serum gamma-glutamyltransferase', 'PFIC3', 'progressive familial intrahepatic cholestasis caused by mutation in ABCB4', 'cholestasis, progressive familial intrahepatic, type 3', 'cholestasis, progressive familial intrahepatic, 3', 'cholestasis, progressive familial intrahepatic, with elevated serum gamma-glutamyltransferase', 'Mdr3 deficiency', 'ABCB4 progressive familial intrahepatic cholestasis']",0070223,602347,79305,C1865643,"['0.2336', '0.189', '-0.4832', '-0.2168', '-0.126', '-0.518', '-0.1735', '0.6978', '-0.2617', '0.625', '-0.412', '-0.1058', '-0.0746', '0.559', '-0.487', '-0.7334', '-0.3335', '-0.4285', '0.6987', '-1.021', '-0.4124', '-0.1924', '0.75', '-0.1448', '-0.1461', '0.3186', '-0.0632', '0.3152', '-0.4028', '-0.6196', '0.4421', '-0.2585', '0.06012', '0.1868', '-0.758', '-0.1539', '-0.5557', '0.06235', '0.01115', '0.2478', '-0.0456', '-0.1307', '0.6304', '0.231', '0.0194', '0.5205', '-0.2493', '-0.5244', '0.2715', '-0.1646', '0.255', '0.2268', '0.502', '-0.3848', '0.1941', '-0.2646', '0.581', '0.04843', '-0.4312', '0.652', '0.6216', '0.1396', '0.749', '-0.1941', '0.3281', '0.0127', '0.841', '0.4495', '-0.0854', '0.1849', '0.2063', '-0.11646', '-0.07916', '-0.6216', '0.537', '0.3496', '-0.02122', '-0.10126', '-0.02861', '0.2166', '-0.1311', '-0.002655', '-0.8037', '-0.1399', '-0.4958', '-0.1862', '0.2922', '-0.2096', '0.5415', '-0.3262', '0.629', '0.3062', '-0.3044', '-0.0897', '0.852', '0.002844', '0.415', '-0.3662', '-0.2255', '-0.507']",,,C535935,,,,
mondo:0011215,osteocraniostenosis,"['Habrodysplasia', 'skeletal dysplasia lethal with gracile bones', 'skeletal dysplasia, lethal, with gracile bones', 'GCLEB', 'osteocraniostenosis', 'gracile bone dysplasia', 'Osteocraniosplenic syndrome']",,602361,2763,C1865639,"['-0.7607', '-0.0889', '0.1353', '0.1506', '0.4338', '-0.5024', '-0.0688', '0.751', '-0.5894', '-0.3767', '-0.0499', '0.0004225', '0.428', '0.002935', '-0.2974', '0.763', '0.5044', '-0.3728', '-0.6875', '-0.673', '0.4688', '0.03278', '0.5737', '0.07715', '0.3484', '-0.1981', '-0.2815', '-0.01826', '0.983', '-0.01384', '-0.0995', '-0.03784', '0.08673', '-0.41', '0.4277', '-0.3755', '-0.4292', '-0.4084', '0.1576', '0.1692', '-0.09283', '-0.4023', '0.17', '-0.544', '0.3918', '-0.6104', '0.0725', '0.4946', '-0.4253', '-0.4255', '0.1086', '-0.637', '-0.4814', '0.705', '-0.969', '-0.7983', '-0.1777', '0.182', '0.3142', '0.2856', '0.2072', '0.258', '-0.674', '-0.3955', '-0.1895', '-0.585', '0.367', '0.6', '-0.2319', '0.2683', '-0.2035', '-0.05722', '0.3215', '0.1659', '-0.0003104', '0.4573', '-0.07947', '0.2832', '-0.2499', '-0.2222', '0.4092', '0.07904', '0.3467', '0.586', '-0.2673', '-0.06934', '-0.08984', '0.1986', '0.1973', '0.2108', '0.07306', '-0.1161', '0.0914', '0.11005', '1.055', '0.6045', '0.6484', '-0.6035', '0.4922', '-0.331']",,,C537291,,Q78.0,,
mondo:0011216,hemochromatosis type 2A,"['hemochromatosis, type 2', 'hemochromatosis type 2 caused by mutation in HJV', 'HFE2A', 'hemochromatosis, juvenile', 'HJV hemochromatosis type 2', 'hemochromatosis, type 2A']",0111027,602390,,,,,,,,,,
mondo:0011217,desmosterolosis,['desmosterolosis'],,602398,35107,C1865596,"['-0.36', '-0.1252', '0.3467', '-0.267', '0.2031', '-0.3875', '-0.2847', '0.7715', '-0.3665', '-0.1503', '-0.3203', '-0.1904', '-0.171', '-0.2783', '-0.2101', '0.04883', '0.4248', '-0.1196', '0.0989', '-0.6406', '0.1606', '-0.299', '0.0696', '0.0771', '0.274', '-0.2454', '-0.2113', '0.2009', '0.228', '-0.3916', '0.346', '0.014656', '0.3394', '0.2827', '-0.04483', '0.04376', '-0.2644', '0.0818', '-0.3718', '0.0553', '-0.0665', '-0.0921', '-0.0674', '-0.04013', '-0.2927', '-0.2878', '-0.04483', '0.3665', '-0.6226', '0.1962', '-0.3682', '-0.0644', '-0.2109', '-0.014854', '-0.562', '-0.105', '0.2429', '-0.566', '0.0345', '0.2051', '-0.2227', '0.3694', '-0.03427', '0.18', '-0.4126', '-0.1156', '0.0911', '0.6304', '-0.4343', '0.3071', '0.012054', '0.373', '-0.2018', '-0.01406', '-0.1534', '-0.2297', '0.3032', '-0.4478', '-0.3096', '0.02025', '0.2974', '0.07477', '0.02249', '0.4165', '-0.2257', '0.408', '-0.10126', '0.2264', '-0.06934', '0.2595', '0.32', '0.7754', '0.2346', '0.371', '0.838', '0.0299', '0.2742', '-0.238', '0.702', '0.1855']",,,C566555,272.8,,,
mondo:0011218,autosomal recessive congenital ichthyosis 11,"['IHS', 'ichthyosis, congenital, autosomal recessive type 11', 'ARCI11', 'IFAH syndrome', 'hypotrichosis-congenital ichthyosis syndrome', 'autosomal recessive congenital ichthyosis type 11', 'ichthyosis-follicular atrophoderma-hypotrichosis syndrome', 'ichthyosis with hypotrichosis, autosomal recessive', 'ichthyosis, congenital, autosomal recessive 11', 'ARIH', 'ichthyosis-follicular atrophoderma-hypotrichosis-hypohidrosis syndrome', 'autosomal recessive ichthyosis with hypotrichosis', 'ichthyosis-hypotrichosis syndrome', 'ichthyosis and follicular atrophoderma with hypotrichosis and hypohidrosis']",0060720,602400,91132,C1835851,"['-0.1764', '0.2966', '-0.12494', '0.1538', '0.1462', '-0.3433', '-0.2795', '0.0648', '0.04987', '-0.3987', '-0.09424', '0.0219', '0.0957', '-0.219', '0.1329', '0.1043', '0.06213', '0.01378', '-0.305', '-0.2106', '-0.005802', '-0.2812', '0.1876', '-0.2211', '0.2507', '0.0522', '-0.2269', '-0.006104', '0.1542', '-0.3918', '0.4265', '-0.10297', '-0.03677', '-0.03023', '-0.02083', '-0.2644', '0.1155', '-0.2778', '0.11316', '-0.3157', '0.1058', '-0.4482', '0.06555', '-0.2291', '0.00218', '-0.3716', '0.03436', '-0.1148', '0.009964', '-0.3303', '-0.1083', '-0.3945', '-0.04398', '0.181', '0.149', '-0.2131', '0.646', '0.02054', '-0.3806', '0.0888', '0.228', '0.02347', '0.1051', '0.0532', '0.2534', '0.10504', '0.1732', '0.0536', '-0.3472', '0.2688', '-0.4187', '-0.1508', '-0.07684', '0.274', '0.09033', '0.2708', '-0.0862', '0.3108', '0.0918', '0.02773', '0.3206', '0.204', '0.051', '0.2913', '-0.0733', '0.108', '0.2081', '0.4724', '0.1561', '-0.01333', '0.1267', '0.2976', '0.03848', '-0.06433', '0.693', '0.1274', '0.2052', '-0.6333', '-0.0956', '-0.1498']",,,C536273,,,,
mondo:0011219,Fried^s tooth and nail syndrome,"['ECTD8', 'ectodermal dysplasia 8, hair/tooth/nail type']",0111661,602401,99672,C0406715,,,,,,,,
mondo:0011220,"parkinson disease 3, autosomal dominant","['PARK3', 'Parkinson disease type 3', 'Parkinson disease 3, autosomal dominant', 'autosomal dominant Parkinson disease', 'Parkinson disease 3, autosomal dominant Lewy body', 'Parkinson disease 3']",0111250,602404,,C1865581,,,,C566552,,,,
mondo:0011221,Weyers ulnar ray/oligodactyly syndrome,['Weyers ulnar ray/oligodactyly syndrome'],,602418,,C1865566,,,,C536696,,,,
mondo:0011223,amyotrophic lateral sclerosis type 4,"['SETX amyotrophic lateral sclerosis', 'neuronopathy, distal hereditary motor, with pyramidal features', 'amyotrophic lateral sclerosis 4', 'distal hereditary motor neuropathy with upper motor neuron signs', 'amyotrophic lateral sclerosis caused by mutation in SETX', 'amyotrophic lateral sclerosis 4, juvenile', 'ALS 4', 'distal hereditary motor neuropathy with pyramidal features', 'ALS4', 'dHMN with upper motor neuron signs']",0060196,602433,357043,C1865409,"['-0.6665', '0.2448', '0.2192', '-0.2695', '-0.1572', '-0.4612', '-0.015564', '0.4502', '-0.6733', '-0.02086', '0.01862', '0.03442', '-0.3367', '-0.06854', '0.718', '-0.3225', '-0.02182', '-0.1925', '-0.1833', '-0.5864', '0.62', '-0.3005', '0.02347', '0.2411', '0.17', '0.1969', '0.1727', '0.002272', '-0.72', '0.1466', '0.01242', '0.10236', '0.2568', '0.05585', '0.2788', '-0.2798', '-0.3794', '0.04605', '-0.00594', '-0.438', '-0.10645', '-0.2722', '-0.253', '0.4048', '-0.1345', '-0.296', '0.2152', '0.1235', '0.129', '0.2847', '0.2098', '0.4456', '-0.08826', '-0.2198', '-0.2754', '-0.755', '0.364', '-0.1663', '-0.4207', '0.06824', '-0.128', '0.1265', '0.2314', '0.0979', '-0.6895', '0.3833', '0.3357', '0.2026', '-0.3325', '0.132', '-0.4417', '0.1394', '0.305', '-0.3499', '0.231', '0.05624', '0.1953', '0.6284', '-0.2405', '-0.2593', '-0.01653', '-0.2279', '0.569', '0.508', '-0.1682', '-0.3857', '-0.01567', '0.228', '0.407', '0.04956', '0.2437', '0.04977', '0.1803', '-0.04578', '0.389', '0.3315', '0.5703', '0.002537', '0.1626', '0.3254']",,,C566550,,,,
mondo:0011224,monomelic amyotrophy,"['spinal muscular atrophy, juvenile, nonprogressive', 'juvenile muscular atrophy of the distal upper limb', 'Hirayama disease', 'spinal muscular atrophy juvenile nonprogressive', 'benign focal amyotrophy', 'JMADUE', 'amyotrophy, monomelic', 'juvenile muscular atrophy of distal upper extremity']",,602440,65684,C1865384,,,1001989,C538253,,,10069681,
mondo:0011225,severe combined immunodeficiency due to DCLRE1C deficiency,"['SCID due to DCLRE1C deficiency', 'SCID due to ARTEMIS deficiency', 'severe combined immunodeficiency, Athabascan type', 'SCID, Athabaskan type', 'severe combined immunodeficiency due to artemis deficiency', 'severe combined immunodeficiency with sensitivity to ionizing radiation', 'severe combined immunodeficiency, Athabaskan-type', 'DCLRE1C severe combined immunodeficiency (disease)', 'SCID, Athabascan type', 'severe combined immunodeficiency with sensitivity to ionising radiation', 'severe combined immunodeficiency due to ARTEMIS deficiency', 'severe combined immunodeficiency due to DCLRE1C deficiency', 'severe combined immunodeficiency, Athabaskan type', 'SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with sensitivity to ionising radiation', 'SCID due to artemis deficiency', 'SCID, autosomal recessive, T cell-negative, B cell-negative, NK cell-positive, with sensitivity to ionizing radiation', 'artemis deficiency', 'severe combined immunodeficiency, partial', 'RS-SCID', 'Athabaskan Severe combined immunodeficiency']",0090012,602450,275,,"['-0.603', '-0.001595', '0.2499', '-0.758', '0.24', '-0.4197', '0.51', '-0.0858', '0.2225', '-0.3884', '0.3416', '-0.3496', '-0.4475', '0.0261', '-0.3884', '-0.1001', '0.473', '-0.1606', '0.0469', '-0.6543', '-0.1892', '-0.543', '0.628', '-0.6543', '0.5107', '0.2042', '-0.1659', '0.0745', '-0.05466', '-0.3853', '0.1808', '0.7266', '0.706', '-0.04343', '-0.09216', '-0.7227', '-0.3054', '-0.0527', '-0.4685', '-0.2925', '-0.6567', '-0.1538', '0.1249', '-0.1105', '-0.585', '-0.3638', '-0.0884', '-0.584', '0.2993', '0.2004', '0.09515', '-0.463', '0.4043', '0.00996', '-0.3674', '-0.0711', '0.1732', '-0.1461', '-0.1727', '0.2123', '-0.2229', '0.3904', '0.02383', '-0.03488', '0.833', '-0.1542', '0.512', '0.4695', '-0.252', '0.5244', '-0.826', '-0.1565', '-0.009254', '-0.344', '0.04825', '-0.1117', '0.11884', '-0.3826', '0.0908', '0.524', '-0.1111', '-0.0546', '-0.1659', '-0.2311', '-0.2673', '-0.2295', '0.8613', '0.3374', '0.682', '-0.1987', '0.04248', '0.3218', '-0.265', '-0.1414', '0.837', '1.012', '0.0906', '-0.907', '-0.05515', '0.05237']",,,,,,,
mondo:0011226,autosomal dominant nonsyndromic hearing loss 15,"['DFNA15', 'autosomal dominant nonsyndromic deafness caused by mutation in POU4F3', 'deafness, autosomal dominant 15', 'autosomal dominant deafness 15', 'deafness, autosomal dominant type 15', 'autosomal dominant nonsyndromic deafness type 15', 'POU4F3 autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness 15']",0110546,602459,,C1865366,,,,C566545,,,,
mondo:0011227,short stature-auditory canal atresia-mandibular hypoplasia-skeletal anomalies syndrome,"['SAMS syndrome', 'short stature, auditory canal atresia, mandibular hypoplasia, skeletal abnormalities', 'short stature, auditory canal atresia, mandibular hypoplasia, and skeletal abnormalities', 'SAMS']",,602471,397623,C1865361,"['-0.37', '0.01878', '0.776', '-0.2301', '0.308', '-0.1587', '0.2402', '0.53', '-0.3435', '-0.2708', '-0.09326', '-0.2607', '-0.1661', '0.01134', '-0.2637', '-0.0573', '0.2239', '-0.1342', '-0.1935', '-0.498', '0.10516', '0.113', '0.266', '-0.12415', '0.2406', '0.06018', '-0.199', '-0.173', '0.339', '-0.129', '0.1869', '-0.1519', '0.1798', '0.2715', '0.364', '-0.2864', '0.03308', '-0.1816', '-0.1423', '-0.4705', '0.1177', '-0.24', '0.1976', '-0.07275', '0.0548', '-0.4673', '-0.039', '0.479', '-0.187', '0.1472', '-0.332', '-0.05154', '0.1335', '0.010216', '-0.4656', '-0.3538', '-0.1262', '-0.04837', '-0.2404', '0.001494', '0.3066', '0.04407', '-0.5615', '0.2227', '-0.205', '-0.131', '0.118', '0.4165', '0.0526', '0.2598', '-0.3123', '0.213', '0.2852', '-0.267', '-0.1161', '-0.2776', '0.0674', '-0.2197', '-0.4314', '-0.1926', '-0.10443', '0.2101', '0.00872', '0.5654', '-0.2372', '0.0698', '-0.1504', '0.522', '0.02963', '0.02908', '-0.1146', '0.633', '0.1681', '0.1897', '0.5127', '-0.1583', '0.667', '-0.4504', '0.4836', '0.2798']",,,C566544,,,,
mondo:0011228,"creases, infra-auricular cutaneous, with tall stature and advanced bone age","['creases, infra-auricular cutaneous, with tall stature and advanced bone age']",,602472,,C1865360,,,,C566543,,,,
mondo:0011229,ethylmalonic encephalopathy,"['syndrome of encephalopathy, petechiae, and ethylmalonic aciduria', 'encephalopathy, petechiae, and ethylmalonic aciduria', 'EPEMA syndrome', 'encephalopathy, ethylmalonic', 'eme', 'EE']",0060640,602473,51188,C1865349,"['-0.2666', '0.2352', '-0.3801', '-0.245', '-0.0258', '-0.303', '-0.784', '0.7764', '-0.2905', '-0.2455', '-0.4724', '-0.3765', '0.1978', '-0.1886', '-0.2559', '-0.1454', '0.09314', '0.1267', '-0.6465', '-0.7573', '0.654', '-0.6777', '0.181', '-0.2412', '0.3916', '-0.0977', '0.25', '0.107', '-0.01543', '-0.274', '0.1971', '-0.2191', '0.12463', '0.03946', '-0.302', '0.269', '-0.2524', '-0.1884', '0.303', '0.3513', '0.09894', '-0.8916', '0.2377', '-0.1104', '-0.1448', '-0.1754', '0.0815', '-0.01433', '-0.53', '-0.1934', '-0.1569', '-0.01964', '-0.732', '-0.08093', '0.4736', '0.3674', '0.6387', '0.2026', '-0.3936', '0.502', '0.276', '0.7285', '0.3315', '-0.7163', '0.1149', '-0.606', '0.608', '0.2338', '-0.2708', '0.195', '-0.09607', '0.3254', '-0.289', '0.1512', '0.08923', '0.1997', '0.787', '0.0551', '-0.2344', '0.483', '0.0285', '0.1622', '0.4434', '0.5474', '-0.165', '0.2646', '0.0945', '0.603', '0.3022', '0.688', '0.623', '0.3442', '-0.1914', '-0.10675', '0.0924', '1.007', '0.10956', '-0.332', '-0.465', '-0.1432']",,,C535737,,,,
mondo:0011230,ossification of the posterior longitudinal ligament of the spine,"['ossification of the POSTERIOR longitudinal ligament of spine', 'OPLL', 'ossification of Posterior longitudinal ligament']",0060887,602475,,C1865343,"['-0.514', '0.3743', '0.2179', '-0.3005', '0.01665', '-0.1486', '0.0886', '0.4268', '-0.7173', '0.06094', '-0.4128', '0.1266', '-0.1569', '0.271', '-0.08124', '-0.07275', '0.03757', '-0.2462', '-0.0754', '-0.3708', '0.08514', '-0.217', '0.1985', '0.0326', '-0.01315', '0.09875', '0.1373', '0.125', '-0.1377', '0.1914', '-0.1208', '-0.06476', '-0.2676', '-0.12085', '0.1174', '-0.0953', '0.263', '-0.04794', '0.1772', '-0.4321', '-0.1465', '-0.1709', '0.0668', '0.0451', '0.04507', '-0.08923', '0.0237', '0.2986', '0.2284', '0.1796', '0.1006', '0.2507', '0.005405', '0.1023', '-0.08093', '-0.3677', '0.3083', '0.07336', '-0.1466', '0.1714', '0.0555', '0.077', '-0.394', '0.05664', '-0.3308', '0.1315', '0.2793', '0.7075', '0.01578', '0.1296', '-0.1945', '0.163', '0.247', '-0.1776', '0.0795', '0.238', '0.000653', '0.253', '0.09106', '-0.419', '-0.364', '-0.1191', '0.371', '0.3645', '-0.10767', '-0.0326', '-0.1631', '-0.04272', '0.4185', '-0.12103', '-0.1501', '0.1587', '0.116', '0.09235', '0.4082', '-0.2347', '0.4119', '-0.2732', '-0.03955', '0.0566']",C84975,0005895,C537143,,,,
mondo:0011231,"febrile seizures, familial, 2","['FEB2', 'generalised epilepsy with febrile seizures plus, type 11', 'generalized epilepsy with febrile seizures plus, type 11', 'convulsions, familial febrile, 2', 'febrile seizures, familial, 2']",0111310,,,C1865342,,,,C566541,,,,
mondo:0011232,"migraine, familial hemiplegic, 2","['migraine, familial hemiplegic, type 2', 'hemiplegic migraine, familial type 2', 'FHM2', 'familial or sporadic hemiplegic migraine caused by mutation in ATP1A2', 'ATP1A2 familial or sporadic hemiplegic migraine', 'migraine, familial basilar', 'familial hemiplegic migraine type 2', 'Mhp2', 'migraine, familial hemiplegic, 2']",0111182,602481,,C1865322,,,,,,,,
mondo:0011233,Axenfeld-Rieger syndrome type 3,"['FOXC1 Axenfeld-Rieger syndrome', 'anterior chamber cleavage syndrome', 'Rieger syndrome, type 3', 'Axenfeld-Rieger anomaly', 'Rieger syndrome type 3', 'anterior segment mesenchymal dysgenesis', 'Axenfeld-Rieger anomaly with Cardiac defects and/Or sensorineural hearing loss', 'Axenfeld-Rieger anomaly with or without cardiac defects and/or sensorineural hearing loss', 'Axenfeld-Rieger anomaly with or without Cardiac defects and/or sensorineural hearing loss', 'anterior chamber Cleavage syndrome', 'Rieger anomaly', 'Axenfeld-Rieger syndrome, type 3', 'RIEG3', 'Axenfeld anomaly', 'Axenfeld-Rieger syndrome caused by mutation in FOXC1']",0110122,602482,98978,,"['-0.4446', '0.1831', '0.4412', '0.1196', '0.2522', '-0.02103', '-0.325', '-0.1182', '-0.2405', '-0.1508', '0.079', '-0.144', '0.2512', '-0.0327', '-0.6045', '-0.3784', '-0.1936', '-0.527', '0.4463', '-0.944', '-0.2107', '0.12085', '0.31', '0.1963', '0.1569', '0.02849', '-0.1459', '0.1953', '0.3782', '0.281', '0.01331', '0.1951', '0.005985', '0.1447', '0.1578', '0.1384', '0.223', '0.2544', '0.05103', '-0.775', '0.543', '-0.04703', '0.1329', '0.0757', '-0.05972', '0.001888', '0.2434', '0.1752', '0.3535', '-0.2094', '-0.2299', '-0.1818', '0.06616', '-0.03192', '-0.2157', '-0.525', '0.1813', '0.3958', '-0.7183', '0.02243', '0.2578', '0.362', '-0.0943', '0.401', '0.1465', '-0.1683', '0.944', '0.4507', '-0.292', '0.2683', '-0.532', '0.548', '0.4783', '-0.11597', '-0.336', '0.3347', '-0.0985', '-0.1774', '-0.3123', '-0.12146', '0.2163', '-0.2286', '-0.2444', '0.847', '-0.1886', '-0.2568', '0.1242', '0.1552', '0.05197', '0.3118', '0.4475', '0.543', '0.46', '0.0688', '0.673', '-0.3523', '0.6533', '-0.4124', '0.09674', '0.2382']",,,,743.44,,,
mondo:0011234,auriculocondylar syndrome 1,"['auriculocondylar syndrome caused by mutation in GNAI3', 'AURICULOCONDYLAR syndrome 1', 'Auriculocondylar syndrome 1', 'question Mark ears syndrome', 'Auriculocondylar syndrome type 1', 'GNAI3 auriculocondylar syndrome', 'ARCND1']",,602483,,,,,,,,,,
mondo:0011235,pelvic dysplasia-arthrogryposis of lower limbs syndrome,"['Ray-Peterson-Scott syndrome', 'pelvic dysplasia arthrogryposis of lower limbs', 'pelvic hypoplasia with lower limb arthrogryposis', 'pelvic hypoplasia with arthrogryposis of lower limbs', 'pelvic hypoplasia with LOWER-limb arthrogryposis']",,602484,2840,C1865294,,,,,,,,
mondo:0011236,hyperinsulinism due to glucokinase deficiency,"['hyperinsulinemic hypoglycemia due to glucokinase deficiency', 'hyperinsulinemic hypoglycemia familial 3', 'hyperinsulinemic hypoglycemia, familial, 3', 'hyperinsulinemic hypoglycemia, familial, type 3', 'HHF3']",0070216,602485,79299,,"['-0.1575', '0.5415', '-0.4966', '0.3926', '-0.6274', '-0.328', '-0.03598', '0.3254', '0.06027', '-0.5913', '-0.428', '-0.2168', '0.5557', '0.409', '0.3516', '-0.04922', '0.3196', '0.2177', '0.05115', '-0.353', '0.498', '-0.01663', '0.6494', '0.0668', '-0.5317', '0.3127', '-0.1648', '-0.3242', '-0.0755', '-0.5776', '0.4014', '0.6494', '0.2637', '0.4443', '-0.557', '-0.2834', '-0.202', '0.14', '-0.164', '0.4116', '-0.2458', '-0.3909', '0.3335', '0.1082', '-0.3684', '0.02855', '-0.005253', '0.00983', '0.271', '0.4844', '-0.1637', '-0.2418', '-0.4092', '-0.1993', '-0.1641', '0.5083', '0.5815', '-0.359', '-0.4453', '0.4553', '-0.1766', '0.524', '-0.1741', '-0.6597', '0.6216', '0.2108', '-0.004818', '0.4363', '-0.7173', '-0.05136', '-0.3784', '0.3042', '0.2177', '-0.435', '0.4873', '0.3962', '0.1395', '0.2976', '-0.2698', '0.2023', '0.10284', '-0.11523', '-0.837', '0.05072', '-0.2443', '0.505', '0.0663', '0.2854', '1.157', '0.315', '0.949', '0.5137', '-0.4287', '0.03638', '0.07806', '-0.0649', '0.592', '-0.9624', '0.0639', '0.5195']",,,C538374,,,,
mondo:0011237,"hyperlipidemia, combined, 1","['hyperlipidemia, familial combined, susceptibility to', 'hyperlipidemia, combined, type 1', 'familial combined hyperlipidemia caused by mutation in USF1', 'hyperlipidemia, familial combined, 1', 'hyplip1', 'USF1 familial combined hyperlipidemia', 'hyperlipidemia, combined, 1']",,602491,,C1865289,,,,C566535,,,,
mondo:0011238,"chondrodysplasia punctata, brachytelephalangic, autosomal","['chondrodysplasia punctata, brachytelephalangic, autosomal', 'brachytelephalangic chondrodysplasia punctata']",,602497,,C1844853,,,,,,,,
mondo:0011239,colobomatous macrophthalmia-microcornea syndrome,"['MACOM', 'MACOM syndrome', 'macrophthalmia, colobomatous, with microcornea']",,602499,468672,C1865286,,,,C566533,,,,
mondo:0011240,megalencephaly-capillary malformation-polymicrogyria syndrome,"['macrocephaly-cutis marmorata telangiectatica congenita syndrome', 'MCMTC', 'M-CM', 'macrocephaly-capillary malformation', 'MCAP', 'macrocephaly-cutis marmorata telangiectatica congenita', 'megalencephaly-cutis marmorata telangiectatica congenita', 'megalocephaly cutis marmorata telangiectatica congenita', 'megalencephaly-capillary malformation-polymicrogyria syndrome', 'megalencephaly-cutis marmorata telangiectatica congenita syndrome', 'megalencephaly cutis marmorata telangiectatica congenita', 'macrocephaly cutis marmorata telangiectatica congenita', 'MCM', 'M-CMTC', 'megalencephaly-capillary malformation syndrome', 'megalencephaly-capillary malformation-polymicrogyria syndrome, somatic', 'macrocephaly-capillary malformation syndrome']",,602501,60040,C1865285,"['0.578', '0.4426', '-0.003826', '0.1698', '0.0772', '-0.3396', '0.0874', '0.629', '-0.6865', '0.1225', '0.05066', '0.2019', '0.5913', '-0.02051', '0.2401', '-0.2333', '0.596', '-0.678', '-0.0886', '-0.368', '0.014534', '0.2068', '0.2683', '-0.10474', '0.03995', '-0.553', '-0.1302', '0.3577', '0.3062', '-0.0549', '0.691', '-0.3948', '0.546', '0.1522', '0.0495', '0.3853', '-0.1001', '0.4329', '-0.69', '-0.0807', '0.135', '-0.1075', '0.3748', '-0.0228', '0.6123', '-0.0851', '-0.063', '0.291', '-0.432', '-0.4155', '-0.6235', '0.1687', '-0.718', '0.1389', '-0.752', '0.1041', '-0.5254', '-0.1846', '-0.3386', '-0.1195', '0.1777', '0.229', '-0.3464', '-0.138', '-0.405', '0.1237', '0.0568', '0.07965', '-0.783', '0.11523', '-0.157', '0.4102', '0.1685', '-0.1827', '0.01756', '-0.42', '0.2336', '-0.0487', '-0.6597', '-0.644', '-0.1898', '-0.2455', '-0.07324', '0.3296', '-0.2642', '-0.02417', '-0.3428', '0.591', '0.02112', '0.3162', '0.727', '0.2292', '-0.1625', '-0.005737', '0.3865', '-0.1263', '0.8613', '-0.3042', '0.2737', '0.5947']",,,C536142,759.89,,,
mondo:0011241,pseudoacromegaly with severe insulin resistance,['pseudoacromegaly with severe insulin resistance'],,602511,,C1865284,,,,C566531,,,,
mondo:0011242,Bartter disease type 4A,"['sensorineural deafness with mild renal dysfunction', 'BARTS4A', 'BSND Bartter syndrome', 'Bartter syndrome, type 4A, neonatal, with sensorineural deafness', 'Bartter syndrome, type 4A', 'Bartter syndrome, infantile, with sensorineural deafness', 'Bartter syndrome caused by mutation in BSND', 'BSND', 'Bartter syndrome type 4a', 'neonatal Bartter syndrome with sensorineural deafness', 'Bartter syndrome, neonatal, with sensorineural deafness']",0110145,602522,,C1865270,,,,,,,,
mondo:0011243,grange syndrome,"['grange occlusive arterial syndrome', 'GRNG', 'grange syndrome', 'progressive arterial occlusive disease-hypertension-heart defects-bone fragility-brachysyndactyly syndrome', 'arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly']",,602531,79094,C1865267,"['0.02614', '-0.2754', '0.2432', '-0.4053', '0.3508', '-0.449', '-0.259', '0.5103', '0.344', '-0.3962', '-0.403', '-0.6216', '0.0961', '0.074', '0.04642', '0.1278', '0.1527', '0.276', '-0.0552', '-0.4326', '0.1749', '0.1731', '0.0853', '-0.625', '0.05692', '0.1765', '0.08374', '0.2534', '0.4033', '-0.322', '0.5845', '-0.3088', '0.536', '0.1504', '-0.2128', '-0.3171', '0.1385', '-0.1884', '-0.0579', '-0.1259', '0.3486', '-0.3042', '0.2162', '-0.431', '-0.0727', '-0.5586', '0.2837', '0.082', '-0.5396', '-0.4673', '-0.113', '-0.004707', '0.2776', '0.3318', '0.08655', '0.02136', '0.2815', '0.2603', '-0.1787', '0.2693', '0.006874', '-0.0315', '-0.02475', '-0.2291', '-0.3267', '-0.1741', '0.08057', '0.841', '-0.8647', '0.2832', '-0.2383', '0.2252', '-0.5317', '-0.2383', '0.079', '-0.013756', '-0.03244', '-0.06506', '0.04483', '0.1862', '-0.3079', '0.603', '0.5454', '0.9478', '-0.08484', '0.1326', '0.475', '0.251', '-0.3335', '-0.194', '-0.1902', '0.2307', '0.1847', '0.04297', '1.0205', '0.3403', '0.5283', '-0.3972', '0.1943', '0.0643']",,,C566529,,,,
mondo:0011244,Marshall-Smith syndrome,"['accelerated skeletal maturation-facial dysmorphism-failure to thrive syndrome', 'MRSHSS', 'Marshall-SMITH syndrome', 'Marshall-Smith syndrome']",0050858,602535,561,C0265211,"['0.0671', '-0.3357', '0.1898', '-0.0172', '0.05298', '-0.3303', '0.273', '1.132', '-0.415', '-0.2866', '-0.1488', '-0.347', '-0.01482', '-0.2418', '-0.1458', '0.1572', '0.2129', '-0.02554', '-0.2488', '-0.715', '-0.01238', '-0.04675', '0.581', '-0.4165', '0.0525', '-0.589', '0.08966', '0.3203', '0.6445', '-0.3242', '0.2052', '-0.171', '0.5845', '-0.2625', '0.1721', '0.04138', '0.02536', '-0.695', '0.0763', '-0.3657', '-0.02623', '-0.02556', '0.1567', '0.0697', '0.06433', '-0.1954', '0.1195', '0.2727', '0.02318', '0.1396', '-0.2588', '0.2407', '-0.1843', '0.2346', '-0.417', '-0.1873', '-0.5176', '-0.3777', '0.2656', '0.0669', '-0.0817', '0.4685', '-0.5015', '-0.264', '0.04758', '0.2406', '0.3232', '0.3157', '-0.4917', '0.4148', '-0.1896', '0.4546', '-0.2035', '0.0383', '-0.4563', '-0.469', '0.4592', '-0.2983', '-0.03427', '0.176', '-0.4878', '-0.04926', '0.02846', '0.756', '-0.3555', '0.0507', '0.2756', '0.0972', '0.4739', '0.2151', '0.0243', '0.2108', '-0.2494', '-0.1315', '0.4888', '-0.003124', '0.279', '0.1458', '0.7817', '0.0837']",,,C536026,759.89,,,
mondo:0011245,"ichthyosis, hystrix-like, with hearing loss","['HID syndrome', 'ichthyosis, hystrix-like, with deafness', 'hystrix-like ichthyosis with deafness']",,602540,,C1865234,,,,C566528,,,,
mondo:0011246,megaconial type congenital muscular dystrophy,"['megaconial congenital muscular dystrophy', 'muscular dystrophy, congenital, megaconial type', 'megaconial congénital muscular dystrophy', 'congenital muscular dystrophy with mitochondrial structural abnormalities', 'congenital megaconial myopathy', 'muscular dystrophy, congenital, with mitochondrial structural abnormalities', 'MDCMC', 'congenital muscular dystrophy due to phosphatidylcholine biosynthesis defect']",0110632,602541,280671,C1865233,"['-0.1859', '-0.8623', '-0.4753', '-0.2786', '0.699', '-1.204', '0.11646', '0.4092', '-1.658', '-0.6846', '0.301', '0.12024', '-0.2032', '0.81', '0.2285', '0.2391', '-0.942', '-0.3625', '-0.5645', '-0.7715', '0.09534', '0.3157', '0.2688', '0.503', '0.1696', '-0.2065', '-0.2091', '-0.9316', '0.4055', '-0.2186', '0.7983', '-0.2081', '0.7495', '-0.09296', '0.265', '0.0674', '-0.4634', '0.3738', '0.1885', '-0.5786', '0.06128', '-0.352', '-0.4753', '0.583', '-0.3591', '0.463', '0.0734', '0.7954', '-0.1919', '0.5483', '0.2445', '-0.4094', '0.1997', '-0.791', '0.02837', '-0.4622', '0.498', '0.8413', '-0.261', '-0.04968', '-0.01387', '-0.1381', '-0.2627', '0.03452', '0.09076', '-0.06354', '0.2281', '0.5864', '-0.537', '-0.05106', '-0.3513', '0.3872', '0.334', '-0.2527', '0.5283', '0.335', '-0.0099', '0.416', '0.09186', '0.0992', '0.12335', '0.1741', '-0.2047', '-0.01622', '0.04196', '-0.014694', '-0.09485', '-0.2769', '1.119', '0.323', '-0.2505', '0.2686', '0.4373', '0.882', '-0.4224', '0.006615', '0.3044', '-0.682', '-0.1785', '-0.1167']",,,C566527,,,,
mondo:0011247,jejunal atresia with renal adysplasia,['jejunal atresia with renal adysplasia'],,602551,,C1865209,,,,C537567,,,,
mondo:0011248,distal monosomy 13q,"['telomeric deletion13q', 'monosomy 13q32', 'deletion 13q32', 'anal atresia, hypospadias, and penoscrotal inversion', 'distal monosomy type 13q', 'distal 13q deletion', '13q32 deletion']",,602553,1590,C1865208,,,,C566526,,,,
mondo:0011249,torsion dystonia with onset in infancy,['torsion dystonia with onset in infancy'],0090058,602554,,C1865205,,,,C536969,,,,
mondo:0011250,"microcephaly, macrotia, and intellectual disability","['microcephaly, macrotia, and intellectual disability', 'microcephaly, macrotia, and mental retardation']",,602555,,C1865204,,,,C566525,,,,
mondo:0011251,"facial dysmorphism, cleft palate, hearing loss, and camptodactyly","['facial dysmorphism, cleft palate, hearing loss, and camptodactyly']",,602556,,C1865203,,,,C566524,,,,
mondo:0011252,"spondyloepimetaphyseal dysplasia, Shohat type","['spondyloepimetaphyseal dysplasia Shohat type', 'spondyloepimetaphyseal dysplasia, Shohat type', 'SEMD, Shohat type', 'SEMD Shohat type', 'SEMDSH']",,602557,93352,C1865185,"['-0.821', '0.3738', '0.0745', '-0.179', '0.5977', '-0.735', '-0.2404', '0.87', '-0.4487', '-0.357', '-0.1193', '0.0559', '0.199', '-0.516', '-0.1254', '0.5503', '0.1761', '0.089', '-0.593', '-0.1615', '-0.1037', '-0.3118', '0.4783', '-0.4019', '-0.1682', '-0.03976', '0.2644', '0.411', '-0.1538', '-0.5854', '0.6816', '-0.7817', '0.2751', '0.3613', '0.1373', '-0.3535', '-0.595', '-1.161', '-0.2866', '-0.249', '-0.1409', '-0.464', '-0.06274', '-0.105', '-0.4402', '0.2676', '-0.0883', '0.09436', '0.06223', '-0.543', '0.3848', '-0.01645', '0.01791', '0.69', '0.09564', '-1.099', '-0.2808', '-0.3696', '0.0927', '0.2727', '0.0838', '-0.156', '-0.6294', '-0.2656', '-0.517', '-0.00578', '-0.0849', '0.4258', '-0.11993', '0.4697', '-0.597', '-0.1222', '-0.0756', '-0.2954', '-0.137', '0.4138', '-0.3728', '0.5605', '0.003218', '-0.1678', '-0.03528', '-0.0649', '-0.0913', '0.1562', '-0.01216', '0.3574', '0.3054', '0.4468', '0.4856', '-0.3103', '-0.325', '-0.1832', '-0.07654', '0.508', '0.991', '0.2566', '0.09094', '-0.7856', '0.4065', '0.04013']",,,C566523,,,,
mondo:0011253,craniomicromelic syndrome,['craniomicromelic syndrome'],,602558,1524,C1865184,,,,C566522,,,,
mondo:0011254,"brachydactyly, intraventricular septal defect, and deafness","['brachydactyly, intraventricular septal defect, and deafness']",,602561,,C1865182,,,,C566521,,,,
mondo:0011255,mandibulofacial dysostosis-macroblepharon-macrostomia syndrome,"['mandibulofacial dysostosis with macroblepharon and macrostomia', 'Verloes-Lesenfants syndrome', 'macroblepharon, ectropion, hypertelorism, and macrostomia', 'macroblepharon-ectropion-hypertelorism-macrostomia syndrome']",,602562,357158,C1865181,,,,C566520,,,,
mondo:0011256,"emphysema, congenital, with deafness, penoscrotal web, and intellectual disability","['emphysema, congenital, with deafness, penoscrotal web, and mental retardation', 'emphysema, congenital, with deafness, penoscrotal web, and intellectual disability']",,602564,,C1865180,,,,C566519,,,,
mondo:0011257,MPI-congenital disorder of glycosylation,"['CDG-Ib', 'CDG, gastrointestinal type', 'congenital disorder of glycosylation type IB', 'SLSJ syndrome', 'Mannosephosphate isomerase deficiency', 'CDG 1B', 'Saguenay-Lac Saint-Jean syndrome', 'CDG gastrointestinal type', 'MPI-CDG', 'phosphomannose isomerase deficiency', 'Mpi deficiency', 'MPI-CDG (CDG-Ib)', 'Slsj syndrome', 'Protein-losing enteropathy-hepatic fibrosis syndrome', 'CDG1B', 'Saguenay Lac Saint Jean syndrome', 'congenital disorder of glycosylation type 1b', 'carbohydrate deficient glycoprotein syndrome type IB', 'congenital disorder of glycosylation, type IB', 'CDG Ib', 'CDG syndrome type IB', 'carbohydrate-deficient glycoprotein syndrome type 1B']",0080554,602579,79319,,"['-0.2563', '0.2329', '-0.0932', '-0.0972', '-0.0666', '-0.1088', '-0.1338', '0.1335', '-0.1231', '0.1322', '-0.10474', '-0.1594', '0.1605', '-0.1427', '-0.3394', '-0.2239', '0.1896', '0.0806', '-0.05634', '-0.5703', '0.2078', '-0.2388', '0.322', '-0.0617', '0.1736', '-0.03198', '-0.2015', '0.2401', '0.0491', '-0.1763', '0.2205', '0.2708', '0.483', '0.0649', '-0.1481', '-0.3171', '-0.3118', '-0.2062', '-0.2893', '0.06287', '-0.2035', '-0.144', '0.3474', '0.0264', '-0.2922', '0.0393', '-0.1389', '-0.03964', '0.09186', '0.3154', '-0.1713', '0.2673', '0.03787', '-0.06256', '-0.02736', '-0.0377', '0.1062', '-0.1487', '-0.4385', '0.2815', '0.10376', '0.2175', '0.2413', '-0.159', '0.12036', '-0.1038', '0.1327', '0.2415', '-0.4177', '0.189', '-0.337', '0.1067', '0.0692', '-0.1436', '0.1959', '-0.1846', '0.385', '0.0755', '-0.08685', '0.0883', '-0.03806', '-0.1282', '-0.1122', '-0.1054', '-0.0655', '0.1703', '0.3228', '0.2333', '0.3984', '-0.2363', '0.1959', '0.2803', '-0.07043', '-0.1456', '0.207', '0.5474', '0.3638', '-0.618', '0.1678', '0.3674']",,,C535740,277.6,,,
mondo:0011258,branchiootic syndrome 1,"['branchiootic syndrome caused by mutation in EYA1', 'branchiootic syndrome 1', 'bo syndrome 1', 'branchiootic syndrome type 1', 'branchiootic dysplasia', 'EYA1 branchiootic syndrome', 'BOS1', 'anterior segment anomalies with or without cataract']",,602588,,C1865143,,,,,,,,
mondo:0011259,retinitis pigmentosa 22,"['retinitis pigmentosa type 22', 'retinitis pigmentosa 22', 'RP22', 'RP 22']",0110400,602594,,C3887981,,,,,,H35.5,,
mondo:0011260,"pancreatic lymphoma, familial","['hereditary pancreas lymphoma', 'pancreatic lymphoma, familial']",,602596,,C1865139,,,,C566516,,,,
mondo:0011261,"spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability","['spondyloepiphyseal dysplasia-craniosynostosis-cleft palate-cataract-intellectual disability syndrome', 'spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and mental retardation', 'spondyloepiphyseal dysplasia with coronal craniosynostosis, cataracts, cleft palate, and intellectual disability']",0112294,602611,163649,,,,,C566515,,,,
mondo:0011262,"camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye","['camptodactyly, joint contractures, facial skeletal defects', 'camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye', 'Rozin hertz Goodman syndrome']",,602612,1323,C1865133,,,,C535876,,,,
mondo:0011263,"skeletal dysplasia and progressive central nervous system degeneration, lethal","['skeletal dysplasia and progressive central nervous system degeneration, lethal']",,602613,,C1865117,,,,C566514,,,,
mondo:0011264,torsion dystonia 6,"['generalized isolated dystonia caused by mutation in THAP1', 'dystonia 6, torsion', 'primary dystonia, DYT6 type', 'generalised cervical and upper-limb-onset dystonia', 'DYT-THAP1', 'idiopathic torsion dystonia of mixed type', 'torsion dystonia type 6', 'torsion dystonia, adult-onset, mixed type', 'THAP1 generalised isolated dystonia', 'dystonia 6', 'torsion dystonia adult onset mixed type', 'generalized cervical and upper-limb-onset dystonia', 'adolescent-onset dystonia of mixed type', 'generalised isolated dystonia caused by mutation in THAP1', 'THAP1 generalized isolated dystonia', 'DYT6']",0090039,602629,98806,C1414216,"['0.911', '0.1909', '-0.04163', '-0.5186', '-0.05392', '-1.067', '0.5044', '0.1366', '-0.9194', '-0.2104', '1.024', '0.8477', '-0.3618', '0.321', '0.68', '0.828', '0.1346', '-1.026', '-0.561', '-0.924', '-0.399', '-0.1555', '0.322', '-0.07806', '-0.0947', '-0.01562', '-0.03564', '0.1416', '-0.1921', '-0.0647', '0.3367', '0.4116', '0.7964', '-0.1472', '0.626', '0.1294', '0.4377', '-0.284', '0.1973', '-0.2778', '0.3655', '-0.2605', '-0.4512', '0.4092', '0.32', '-0.1792', '-0.481', '0.05267', '0.6553', '0.4072', '-0.00932', '0.1965', '0.2715', '-0.1143', '0.576', '-0.2769', '0.238', '0.6963', '0.2157', '-0.3887', '-0.2341', '-0.5825', '-0.02554', '-0.6846', '-0.891', '0.4905', '0.3347', '0.409', '-0.1686', '0.4495', '-0.334', '-0.331', '-0.02937', '0.2019', '0.0726', '0.3855', '0.7515', '0.12463', '0.08105', '-0.4531', '-0.2917', '0.1761', '0.641', '0.5835', '0.6973', '0.2378', '0.251', '0.2798', '1.502', '-0.0323', '0.4368', '0.1304', '0.356', '0.1621', '1.035', '-0.09546', '-0.1027', '0.2524', '0.495', '-0.262']",C156361,,C538003,,,,
mondo:0011265,"tooth agenesis, selective, 2","['hypodontia/oligodontia 2', 'tooth agenesis, selective, 2', 'STHAG2']",,602639,,C1865092,,,,C566513,,,,
mondo:0011266,myotonic dystrophy type 2,"['dystrophia myotonica type 2', 'DM2', 'ricker syndrome', 'dystrophia myotonica 2', 'proximal myotonic dystrophy', 'PROMM', 'myotonic dystrophy 2', 'myotonic dystrophy type 2', 'proximal myotonic myopathy', 'ricker disease', 'myotonic dystrophy caused by mutation in CNBP', 'CNBP myotonic dystrophy', 'myotonic myopathy, proximal']",0050759,602668,606,C0752355,"['-0.492', '-0.4075', '-0.318', '-0.385', '0.2278', '-0.232', '0.278', '1.081', '-0.1835', '-0.318', '-0.4216', '0.0776', '-0.4685', '-0.03247', '-0.2527', '-0.06036', '-0.3474', '0.215', '-0.6616', '-0.5376', '0.00781', '0.4294', '-0.10236', '-0.1625', '-0.4404', '0.0852', '0.2002', '-0.2495', '0.0613', '-0.6313', '0.725', '-0.01666', '0.1539', '-0.1954', '-0.4758', '-0.1122', '-0.2391', '-0.416', '0.03998', '0.2546', '-0.2499', '-0.6514', '0.424', '0.5776', '0.6216', '0.3682', '-0.086', '0.745', '0.5063', '0.4856', '-0.04355', '0.1825', '-0.0411', '0.0967', '0.2135', '0.11896', '0.3716', '0.1232', '-0.3918', '-0.0453', '0.4155', '-0.2996', '0.0826', '-0.1108', '-0.2322', '0.1702', '0.2888', '0.3738', '-0.5063', '-0.01814', '-0.584', '0.004425', '0.0607', '0.5244', '0.9053', '0.10675', '-0.1189', '0.1842', '0.11145', '-0.4143', '0.1583', '-0.3464', '0.1696', '-0.0096', '-0.0943', '0.4446', '0.2632', '0.05325', '0.3196', '-0.3164', '0.005604', '0.1902', '0.1819', '-0.1433', '0.6484', '-0.1354', '0.694', '-0.1042', '-0.552', '0.1174']",C84680,,,359.2,,,
mondo:0011267,"intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration","['mental retardation, severe, with spasticity and tapetoretinal degeneration', 'mental retardation, severe, with spasticity and pigmentary tapetoretinal degeneration', 'intellectual disability, severe, with spasticity and pigmentary tapetoretinal degeneration', 'Mrst']",,602685,,C1864549,,,,C566429,,,,
mondo:0011268,"renal tubular acidosis, distal, 3, with or without sensorineural hearing loss","['RTADR', 'renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss', 'classical distal renal tubular acidosis', 'type 1 renal tubular acidosis', 'renal tubular acidosis, autosomal recessive, with preserved hearing', 'renal tubular acidosis, distal, autosomal recessive', 'renal tubular acidosis, autosomal recessive with preserved hearing', 'distal renal tubular acidosis 3, with or without sensorineural hearing loss', 'classical distal RTA', 'RTA, distal, autosomal recessive', 'renal tubular acidosis, distal, autosomal recessive, with late-onset sensorineural hearing loss, included', 'type 1 RTA']",,602722,,,,,,,,,,
mondo:0011269,psoriasis 2,"['PSORS2', 'CARD14 psoriasis', 'psoriasis 2', 'psoriasis type 2', 'psoriasis caused by mutation in CARD14']",0080475,602723,,C1864497,,,,,,,,
mondo:0011270,"prostate cancer, hereditary, 8","['prostate cancer, susceptibility to', 'prostate cancer, hereditary, type 8', 'prostate cancer, hereditary, 8', 'predisposing for prostate cancer', 'HPC8']",,602759,,C1864472,,,,C566426,,,,
mondo:0011271,rigid spine muscular dystrophy 1,"['congenital merosin-positive muscular dystrophy with early spine rigidity', 'desmin-related myopathy with Mallory bodies', 'RSS', 'minicore myopathy, severe classic form', 'severe classic form multicore myopathy', 'multicore myopathy, severe classic form', 'RSMD1', 'Eichsfeld type congenital muscular dystrophy', 'muscular dystrophy, congenital, merosin-positive, with early spine rigidity', 'rigid spine muscular dystrophy 1', 'multiminicore disease, severe classic form', 'muscular dystrophy, rigid spine, 1', 'SELENON rigid spine syndrome', 'rigid spine muscular dystrophy type 1', 'rigid spine syndrome caused by mutation in SELENON', 'MDRS1', 'SEPN1-related myopathy', 'myopathy, SEPN1-related', 'severe classic form multiminicore disease', 'classic MmD', 'severe classic form minicore myopathy', 'classic multiminicore myopathy', 'classic multiminicore disease', 'muscular dystrophy, congenital, Eichsfeld type', 'rigid spine syndrome']",0110633,602771,,C0410180,"['-0.010376', '0.02774', '0.005302', '-0.01318', '0.02388', '-0.04825', '0.01151', '0.03738', '-0.04276', '-0.0209', '-0.008835', '-0.005352', '0.001075', '0.0097', '0.004013', '-0.02028', '0.01062', '-0.01817', '-0.0197', '-0.0528', '-0.001527', '-0.01968', '0.03354', '0.002804', '0.002268', '-0.010765', '-0.00866', '-0.02048', '-0.01177', '-0.0224', '0.0228', '-0.003338', '0.02733', '0.0002263', '0.011696', '0.004547', '0.001807', '-0.01144', '0.00891', '-0.04086', '0.01733', '-0.03714', '0.00942', '0.01055', '-0.01316', '-0.007687', '-0.01434', '0.02222', '0.01779', '0.02367', '-0.010025', '-0.001114', '0.00741', '0.00684', '-0.01685', '-0.0176', '0.02998', '-0.01114', '-0.04352', '0.001782', '0.01791', '-0.0002408', '-0.01282', '0.02257', '0.003084', '0.0002213', '0.03793', '0.0443', '-0.03485', '0.03256', '-0.03114', '-0.003633', '0.0277', '-0.014206', '0.03079', '0.02939', '0.00976', '-0.00519', '-0.0316', '-0.02625', '0.003578', '0.000755', '-0.00794', '0.04025', '-0.01964', '-0.00526', '0.005344', '0.03317', '0.04465', '0.006695', '0.001746', '0.02614', '0.01886', '0.01364', '0.0583', '0.014145', '0.0252', '-0.02777', '-0.002394', '0.02069']",C126691,,,,,,
mondo:0011272,retinitis pigmentosa 25,"['retinitis pigmentosa 25', 'EYS retinitis pigmentosa', 'RP25', 'retinitis pigmentosa type 25', 'RP 25', 'retinitis pigmentosa caused by mutation in EYS']",0110384,602772,,C1864446,,,,C566425,,H35.5,,
mondo:0011273,H syndrome,"['histiocytosis-lymphadenopathy plus syndrome', 'Faisalabad histiocytosis', 'hyperpigmentation, cutaneous, with hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism with or without hearing loss', 'HJCD', 'H syndrome', 'Asrar Facharzt Haque syndrome', 'SLC29A3 spectrum disorder', 'histiocytosis and lymphadenopathy with or without cutaneous, Cardiac, and/or endocrine features, Joint contractures, and/or deafness', 'pigmented hypertrichosis with insulin-dependent diabetes mellitus', 'sinus histiocytosis and massive lymphadenopathy', 'histiocytosis with Joint contractures and sensorineural deafness', 'Rosai-Dorfman disease, familial']",0111278,602782,168569,C2930890,"['-0.1816', '0.3462', '-0.03232', '-0.3833', '0.2007', '-0.384', '-0.01749', '0.4624', '-0.2239', '-0.883', '-0.4736', '-0.1203', '-0.3867', '0.0811', '-0.1285', '0.10626', '-0.0668', '0.1599', '0.1841', '-1.107', '0.279', '-0.1891', '0.4795', '0.4968', '0.07465', '1.002', '-0.534', '-0.0742', '-0.2096', '-0.7236', '0.909', '-0.5435', '-0.00928', '-0.2404', '-0.4143', '0.1339', '0.1888', '-0.10583', '-0.2092', '-0.487', '-0.3728', '0.3108', '1.087', '0.09906', '1.067', '-0.2822', '-0.0492', '0.1149', '-0.2063', '-0.0781', '0.1864', '0.538', '0.2375', '0.7173', '0.10443', '-0.2172', '-0.02356', '-0.608', '-0.1401', '0.249', '0.5513', '0.749', '-0.549', '-0.435', '-0.451', '-0.7856', '-0.0437', '0.4841', '-0.3257', '0.921', '-0.359', '-0.1907', '0.068', '-0.0768', '0.4417', '-0.499', '-0.0673', '-0.06183', '-0.10974', '0.06506', '0.5303', '0.02625', '0.332', '-0.01428', '-0.3616', '-0.03357', '0.07983', '-0.1633', '0.2489', '0.1392', '0.4055', '0.1327', '0.4915', '-0.1382', '0.563', '0.3264', '0.06003', '-0.644', '0.1874', '0.2288']",,,C538322,,,,
mondo:0011274,Muenke syndrome,"['Muenke syndrome', 'MNKES', 'syndrome of coronal craniosynostosis', 'Muenke nonsyndromic coronal craniosynostosis', 'FGFR3-related craniosynostosis']",0060703,602849,53271,C1864436,"['0.3362', '0.01834', '0.1984', '0.001007', '0.2034', '0.03873', '0.667', '0.628', '-0.8394', '-0.2252', '0.1864', '0.2546', '0.2349', '0.0341', '-0.1478', '-0.3792', '0.3152', '-0.945', '0.1433', '-0.4895', '-0.0891', '0.0525', '0.2573', '0.003994', '1.119', '-0.03287', '-0.1041', '0.0843', '0.5024', '-0.06885', '0.04013', '-0.45', '0.52', '-0.03757', '-0.02707', '-0.0329', '-0.4126', '-0.8086', '-0.2854', '-0.663', '0.2129', '0.2211', '0.9653', '-0.7266', '0.3347', '-0.1556', '-0.126', '-0.455', '-0.0745', '-0.03314', '-0.006104', '-0.4277', '-0.1902', '-0.5884', '-0.0999', '-0.1725', '-0.2069', '0.0681', '-0.06525', '0.1956', '0.4592', '-0.3384', '-0.1057', '0.4265', '-0.582', '0.10406', '-0.1694', '0.4224', '-0.1929', '0.4324', '-0.07294', '0.8774', '0.1036', '-0.4736', '0.1838', '-0.03177', '0.3767', '-0.335', '-0.7363', '-0.5156', '0.3638', '-0.1892', '-0.2214', '0.5376', '0.03506', '0.5654', '0.02614', '0.74', '0.008194', '0.5894', '-0.485', '0.3115', '-0.3884', '0.000349', '0.4148', '-0.1727', '0.4375', '-0.000308', '0.3435', '0.0726']",C84904,,C537369,,,,
mondo:0011275,"acromesomelic dysplasia 1, Maroteaux type","['acromesomelic dysplasia, Maroteaux type', 'AMDM', 'acromesomelic dwarfism Maroteux type', 'St. Helena dysplasia', 'acromesomelic dysplasia Maroteaux type', 'acromesomelic dysplasia 1, Maroteaux type']",0080050,602875,40,,"['-0.447', '0.7407', '0.3728', '-0.4868', '0.621', '-0.472', '0.1381', '0.7866', '-0.608', '-0.294', '-0.03653', '0.02676', '0.04636', '0.2725', '-0.10046', '0.0384', '0.5854', '0.1138', '-0.515', '-0.518', '-0.3894', '-0.0656', '0.514', '0.042', '-0.1464', '0.3425', '-0.03418', '-0.669', '0.262', '0.1189', '-0.2136', '-0.05978', '0.1627', '0.0514', '0.3462', '-0.2467', '-0.2847', '-0.4521', '-0.10095', '-0.5195', '-0.2783', '-0.569', '-0.1411', '-0.0931', '-0.3406', '-0.3594', '-0.4526', '0.4307', '0.1658', '-0.2467', '0.3718', '-0.00285', '-0.5156', '-0.1465', '-0.3599', '-0.8423', '0.0864', '-0.745', '-0.1635', '0.0216', '0.4429', '0.1353', '-0.2096', '0.2358', '-0.267', '-0.5', '0.04944', '0.05023', '-0.0894', '-0.04022', '-0.4656', '0.2416', '0.402', '-0.6284', '0.1177', '0.4321', '-0.649', '0.1288', '-0.605', '-0.5864', '-0.0454', '0.02939', '0.2954', '0.3567', '-0.05893', '0.3257', '-0.1036', '0.1528', '0.2045', '0.0714', '-0.01099', '0.347', '-0.04974', '0.3086', '0.7617', '0.2122', '0.6997', '-1.048', '0.2656', '0.336']",,,C535661,,,,
mondo:0011276,orofacial cleft 2,"['orofacial cleft 2', 'cleft lip with or without cleft palate, nonsyndromic, 2', 'OFC2']",0080396,602966,,C1864323,,,,C566419,,,,
mondo:0011279,autosomal recessive nonsyndromic hearing loss 17,"['autosomal recessive deafness 17', 'DFNB17', 'deafness, autosomal recessive 17', 'autosomal recessive nonsyndromic deafness 17', 'autosomal recessive nonsyndromic deafness type 17']",0110472,603010,,C1864276,,,,C566418,,,,
mondo:0011280,schizophrenia 6,"['schizophrenia 6', 'schizophrenia susceptibility locus, chromosome 8P-related', 'SCZD6']",0070082,603013,,C1864275,,,,,,,,
mondo:0011281,congenital myasthenic syndrome 5,"['endplate acetylcholinesterase deficiency', 'congenital myasthenic syndrome type 5', 'myasthenic syndrome, congenital, type 5', 'Engel congenital myasthenic syndrome', 'congenital myasthenic syndrome caused by mutation in COLQ', 'Cms Ic', 'end plate acetylcholinesterase deficiency', 'myasthenic syndrome, congenital, Engel type', 'CMS5', 'EAD', 'myasthenic syndrome, congenital, 5', 'congenital myasthenic syndrome type Ic', 'congenital myasthenic syndrome type Ic, formerly', 'congenital myasthenic syndrome Engel type', 'Cms Ic, formerly', 'COLQ congenital myasthenic syndrome', 'CMS Ic']",0110667,603034,,C1864233,,C129304,,C566415,,,,
mondo:0011282,tumor suppressor gene on chromosome 11,"['tumour suppressor Gene on chromosome type 11', 'tumor suppressor gene on chromosome 11', 'Nonsmall cell lung cancer suppressor', 'nonsmall cell lung cancer', 'Tsg11', 'tumor suppressor Gene on chromosome type 11']",,603040,,C1864232,,,,,,,,
mondo:0011283,mitochondrial DNA depletion syndrome 1,"['mitochondrial neurogastrointestinal encephalopathy syndrome, tymp-related', 'Polip syndrome', 'MTDPS1', 'mitochondrial DNA depletion syndrome type 1', 'myoneurogastrointestinal encephalopathy syndrome', 'polyneuropathy, ophthalmoplegia, leukoencephalopathy, and intestinal pseudoobstruction', 'mitochondrial DNA depletion syndrome 1 (MNGIE type)', 'Mngie, tymp-related']",0080119,603041,298,,"['-0.9263', '-0.2289', '-0.556', '0.0964', '0.1722', '-0.1439', '0.5454', '0.518', '-0.515', '0.003126', '-0.11096', '-0.3086', '0.11206', '-0.4746', '0.2358', '0.205', '-0.05786', '0.1725', '-0.8516', '-0.717', '-0.02345', '-0.929', '-0.396', '-0.08246', '0.1818', '-0.3367', '0.1412', '-0.2', '0.46', '-0.28', '0.9487', '0.1857', '0.84', '-0.466', '0.3396', '-0.515', '-0.378', '-0.3804', '0.05432', '0.4438', '-0.2031', '-1.069', '0.531', '0.018', '-0.2347', '0.111', '-0.10846', '-0.1342', '0.0671', '0.03845', '0.311', '0.532', '0.1346', '0.1322', '-0.1903', '-0.5254', '0.484', '0.07635', '-0.3994', '0.6616', '0.53', '0.12134', '0.4114', '0.06137', '-0.6187', '-0.5654', '0.6245', '0.6377', '0.673', '0.6367', '-0.1542', '-0.0482', '0.3809', '0.448', '0.459', '-0.07184', '0.4434', '0.1212', '0.11145', '-0.05426', '0.0597', '-0.765', '0.0737', '0.3323', '-0.12115', '0.599', '0.571', '0.605', '0.2876', '-0.3452', '0.1366', '-0.02063', '-0.1676', '-0.089', '0.02689', '0.2205', '-0.0712', '-0.457', '-0.07153', '0.4744']",,,,,,,
mondo:0011284,astigmatism,"['astigmatism', 'astigmatism (disease)']",11782,603047,,C0004106,,,,D001251,367.20,,,0000483
mondo:0011285,age related macular degeneration 1,"['age related maculopathy 1', 'macular degeneration, age-related, 1', 'macular degeneration, age-related, reduced risk of', 'macular degeneration, age-related', 'macular Degeneration, age-related, type 1', 'maculopathy, age-related, 1', 'ARMD1', 'age related macular degeneration type 1']",0110014,603075,,C1864205,,,,C566411,,,,
mondo:0011286,autosomal recessive nonsyndromic hearing loss 13,"['autosomal recessive nonsyndromic deafness type 13', 'autosomal recessive deafness 13', 'autosomal recessive nonsyndromic deafness 13', 'deafness, autosomal recessive 13', 'DFNB13']",0110468,603098,,C1864199,,,,C566410,,,,
mondo:0011287,craniosynostosis-anal anomalies-porokeratosis syndrome,"['CDAGS syndrome', 'craniosynostosis and clavicular hypoplasia, delayed closure of the fontanel, anal anomalies and genitourinary malformations', 'craniosynostosis, anal anomalies, and porokeratosis', 'CAP syndrome']",,603116,85199,,,,,C536789,,,,
mondo:0011288,"spastic paraplegia, optic atrophy, microcephaly, and 10Y sex reversal","['spastic paraplegia, optic atrophy, microcephaly, and XY SEX reversal']",,603117,,C1864185,,,,C566409,,,,
mondo:0011289,apraxia of eyelid opening,['apraxia of eyelid opening'],,603119,,,,,,,,,,
mondo:0011290,"dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability","['dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and intellectual disability', 'dislocated elbows, bowed tibias, scoliosis, deafness, cataract, microcephaly, and mental retardation']",,603133,,C1864183,,,,C566408,,,,
mondo:0011291,ALG6-congenital disorder of glycosylation 1C,"['CDG-Ic', 'ALG6-CDG (CDG-Ic)', 'glucosyltransferase 1 deficiency', 'carbohydrate-deficient glycoprotein syndrome, type V (formerly)', 'carbohydrate deficient glycoprotein syndrome type Ic', 'carbohydrate-deficient glycoprotein syndrome, type V', 'CDGS5 (formerly)', 'CDG1C', 'carbohydrate-deficient glycoprotein syndrome type 1C', 'congenital disorder of glycosylation, type Ic', 'congenital disorder of glycosylation type 1C', 'congenital disorder of glycosylation caused by mutation in ALG6', 'congenital disorder of glycosylation type Ic', 'carbohydrate-deficient glycoprotein syndrome, type I, with deficient glycosylation of dolichol-linked oligosaccharide, formerly', 'CDGIc', 'carbohydrate-deficient glycoprotein syndrome, type 1 with deficient glycosylation of dolichol-linked oligosaccharide (formerly)', 'carbohydrate-deficient glycoprotein syndrome, type V, formerly', 'ALG6 congenital disorder of glycosylation', 'ALG6-CDG1C', 'carbohydrate-deficient glycoprotein syndrome, type I, with deficient glycosylation of dolichol-linked oligosaccharide', 'ALG6-CDG', 'CDG Ic', 'CDG syndrome type Ic', 'CDG 1C']",0080555,603147,79320,C2930997,"['-0.2632', '-0.0617', '0.2666', '-0.219', '0.03253', '-0.642', '-0.0648', '0.1296', '-0.1361', '-0.3918', '-0.3335', '-0.2251', '-0.1741', '-0.3174', '0.009445', '-0.2145', '0.06525', '-0.3782', '-0.3032', '-0.4626', '0.4812', '-0.2333', '-0.0795', '-0.2294', '0.1238', '-0.02621', '-0.2075', '-0.1383', '0.1189', '-0.0811', '0.11646', '0.1595', '0.2062', '0.1572', '-0.09485', '-0.0404', '-0.2751', '-0.01328', '-0.5', '0.001195', '-0.1675', '-0.4216', '0.1669', '0.04355', '-0.303', '-0.10596', '0.03406', '-0.1698', '0.01952', '0.4854', '-0.384', '0.5107', '-0.10114', '-0.003633', '0.0719', '-0.39', '0.3435', '0.195', '-0.2964', '0.2695', '0.3438', '0.1119', '0.3494', '0.05304', '0.0994', '0.2476', '0.0504', '0.2405', '-0.427', '0.2544', '-0.463', '0.3567', '-0.11993', '-0.06415', '0.06854', '0.00856', '0.4612', '-0.09674', '-0.1637', '0.2314', '-0.1092', '-0.0968', '-0.1714', '0.3445', '-0.2017', '0.12415', '0.0805', '0.4626', '0.2062', '-0.0354', '-0.1166', '0.2988', '-0.09674', '-0.2032', '0.3945', '0.4778', '0.4377', '0.02156', '0.4128', '0.4666']",C126869,,C535741,,,,
mondo:0011292,"dermatitis, atopic","['dermatitis, atopic', 'ATOD', 'eczema, atopic']",,603165,,,,,,D003876,,,,
mondo:0011294,schizophrenia 5,"['schizophrenia 5', 'SCZD5', 'schizophrenia susceptibility locus, chromosome 6Q-related', 'schizophrenia 5 with or without an affective disorder']",0070081,603175,,C1864153,,,,,,,,
mondo:0011295,schizophrenia 7,"['schizophrenia susceptibility locus, chromosome 13Q-related', 'schizophrenia 7', 'schizophrenia 7 with or without an affective disorder', 'SCZD7']",0070083,603176,,,,,,,,,,
mondo:0011296,"Meckel syndrome, type 2","['MKS2', 'Meckel syndrome 2', 'TMEM216 Meckel syndrome', 'Meckel syndrome caused by mutation in TMEM216', 'Meckel-Gruber syndrome, type 2', 'Meckel syndrome type 2', 'Meckel syndrome, type 2']",0070116,603194,,C1864148,,,,C536131,,,,
mondo:0011297,autosomal dominant nocturnal frontal lobe epilepsy 2,"['epilepsy, nocturnal frontal lobe, 2', 'autosomal dominant nocturnal frontal lobe epilepsy type 2', 'epilepsy, nocturnal frontal lobe, type 2', 'ENFL2', 'nocturnal frontal lobe epilepsy 2']",0060683,603204,,C1864125,,,,C566400,,,,
mondo:0011298,schizophrenia 8,"['schizophrenia 8 with or without an affective disorder', 'SCZD8', 'schizophrenia susceptibility locus, chromosome 18-related', 'schizophrenia 8']",0070084,603206,,C1864124,,,,,,,,
mondo:0011299,Huntington disease-like 1,"['early-onset prion disease with prominent psychiatric features', 'Huntington disease-like type 1', 'Huntington^s disease-like 1', 'prion disease, early-onset, with prominent psychiatric features', 'HDL1', 'autosomal dominant Huntington-like neurodegenerative disorder', 'Huntington-like neurodegenerative disorder, autosomal dominant', 'HLN1', 'PRNP neurodegenerative disease with chorea', 'neurodegenerative disease with chorea caused by mutation in PRNP', 'Huntington-like neurodegenerative disorder 1', 'Huntington disease-like 1']",0090103,603218,157941,C1864112,"['-0.3047', '0.5117', '0.4644', '-0.1533', '-0.563', '-0.884', '0.2338', '0.4622', '-0.58', '0.0539', '-0.3257', '-0.2568', '-0.36', '-0.1276', '0.5723', '-0.463', '-0.1304', '-0.3928', '-0.005875', '-0.6035', '0.1057', '-0.3489', '0.11975', '-0.339', '0.4233', '0.2893', '0.1184', '-0.1702', '-0.5146', '0.0857', '0.4211', '0.2598', '0.1038', '-0.0273', '0.2455', '-0.05475', '-0.2878', '-0.2041', '-0.5825', '-0.003815', '0.3535', '-0.383', '0.2142', '0.2156', '0.4648', '-0.2338', '-0.3315', '-0.304', '0.06042', '0.4236', '0.1527', '0.851', '-0.2283', '-0.4094', '0.4878', '-0.2267', '0.4883', '0.0395', '-0.4048', '-0.2268', '0.01765', '0.2295', '0.0499', '-0.1844', '-0.202', '0.2004', '0.477', '-0.0586', '-0.1641', '0.244', '0.02112', '-0.09924', '0.2505', '-0.3025', '0.1296', '0.3154', '0.3281', '0.3894', '-0.2163', '-0.4355', '0.235', '-0.4675', '0.1576', '0.3735', '0.3037', '0.3745', '0.3394', '0.1309', '0.4902', '0.1663', '0.1794', '0.1298', '0.04507', '0.2976', '0.315', '0.2478', '0.2588', '0.1711', '0.11865', '0.4587']",,,C566398,,,,
mondo:0011300,"myopia 3, autosomal dominant","['MYP3', 'myopia-3', 'myopia 3, autosomal dominant']",,603221,,C1864111,,,,C566397,,,,
mondo:0011301,pseudohypoparathyroidism type 1B,"['PHP1B', 'pseudohypoparathyroidism type IB', 'pseudohypoparathyroidism, type IB', 'pseudohypoparathyroidism Ib', 'Php 1B', 'pseudohypoparathyroidism, type 1B']",0080222,603233,94089,C2932715,"['0.162', '0.341', '-0.1823', '-0.3442', '-0.6465', '0.7046', '-0.2615', '0.8223', '-0.771', '-0.939', '-0.4036', '0.01761', '-0.3499', '0.7407', '-0.2397', '0.543', '-0.0503', '-0.571', '-0.325', '-0.5493', '0.2803', '-0.3604', '0.4263', '-0.1213', '0.1503', '-0.2042', '-0.1771', '-0.2092', '0.2686', '-0.7905', '0.148', '0.1975', '-0.1583', '0.1885', '-0.1001', '-0.4817', '0.2734', '0.0521', '0.5996', '0.384', '0.2656', '0.01915', '0.8027', '-0.6553', '0.2524', '-0.595', '0.937', '0.2969', '0.1552', '0.457', '0.0607', '0.575', '1.142', '-0.5225', '-1.082', '-0.363', '0.02835', '-0.6416', '-0.677', '-0.3013', '-0.1553', '-0.401', '0.02498', '-0.4517', '-0.5273', '1.075', '0.4497', '0.6426', '-0.7944', '-0.2318', '-0.05212', '-0.3777', '0.2908', '-0.3267', '0.765', '0.192', '0.255', '0.06168', '0.4617', '0.3354', '0.4187', '0.3623', '0.2375', '-0.9395', '0.05707', '-0.4355', '-0.2524', '0.4702', '0.664', '0.0509', '-0.2311', '0.171', '-0.3494', '-0.5264', '0.1842', '0.2196', '0.11835', '-0.737', '-0.1015', '0.517']",,,C548075,,,,
mondo:0011302,type 1 diabetes mellitus 17,"['IDDM17', 'insulin-dependent diabetes mellitus 17', 'diabetes mellitus, insulin-dependent, 17']",0110754,603266,,C1864068,,,,C566395,,,,
mondo:0011303,focal segmental glomerulosclerosis 1,"['glomerulosclerosis, focal segmental, 1', 'focal segmental glomerulosclerosis 1', 'focal segmental glomerulosclerosis type 1', 'familial idiopathic steroid-resistant nephrotic syndrome with focal segmental glomerulosclerosis', 'familial idiopathic steroid-resistant nephrotic syndrome with focal segmental hyalinosis', 'focal segmental glomerulosclerosis caused by mutation in ACTN4', 'ACTN4 focal segmental glomerulosclerosis', 'FSGS1']",0111128,603278,93213,,,,,C538457,,,,
mondo:0011304,cerebral cavernous malformation 2,"['cerebral cavernous malformations type 2', 'cerebral cavernous malformations-2', 'cerebral cavernous malformations 2', 'cerebral cavernous malformation type 2', 'CCM2 familial cerebral cavernous malformation', 'familial cerebral cavernous malformation caused by mutation in CCM2', 'CCM2']",0060670,603284,,C1864041,,,,C566394,,,,
mondo:0011305,cerebral cavernous malformation 3,"['cerebral cavernous malformation type 3', 'cerebral cavernous malformations-3', 'CCM3', 'familial cerebral cavernous malformation caused by mutation in PDCD10', 'cerebral cavernous malformations 3', 'PDCD10 familial cerebral cavernous malformation', 'cerebral cavernous malformations type 3']",0060671,603285,,C1864040,,,,C566393,,,,
mondo:0011306,"muscular dystrophy, congenital, with cerebellar atrophy","['muscular dystrophy, congenital, with cerebellar atrophy']",,603323,,C1864028,,,,C566392,,,,
mondo:0011307,schizophrenia 2,"['schizophrenia 2', 'schizophrenia susceptibility locus, chromosome 11Q-related', 'SCZD2']",0070078,603342,,C1864010,,,,,,,,
mondo:0011308,GRACILE syndrome,"['Growth retardation, aminoaciduria, cholestasis, iron overload, lactic acidosis and early death', 'gracile syndrome', 'Growth delay-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome', 'FLNMS', 'Fellman syndrome', 'lactic acidosis, Finnish, with hepatic hemosiderosis', 'Fellman disease', 'Finnish lethal neonatal metabolic syndrome', 'Finnish lactic acidosis with hepatic hemosiderosis', 'Growth restriction-aminoaciduria-cholestasis-iron overload-lactic acidosis-early death syndrome', 'Growth retardation, amino aciduria, cholestasis, iron overload, lactic acidosis, and early death']",0111455,603358,53693,C1864002,"['-0.6484', '0.2944', '-0.02002', '0.002972', '0.08704', '-0.7627', '-0.4229', '1.153', '-0.2141', '0.2786', '-0.3647', '-0.6416', '0.1849', '-0.2471', '-0.7114', '-0.09875', '-0.10394', '0.256', '-0.5825', '-0.419', '-0.1378', '-0.7617', '0.542', '-0.0704', '0.05664', '-0.06256', '-0.1001', '0.1807', '0.1721', '-0.4907', '0.3667', '0.01471', '0.3948', '-0.0712', '-0.4788', '0.2009', '-0.1793', '-0.6987', '0.3333', '0.609', '-0.523', '-0.1041', '0.146', '0.1246', '-0.1707', '-0.4888', '0.10175', '0.3347', '-0.2032', '-0.3984', '0.1299', '-0.4856', '-0.278', '-0.3047', '-0.08405', '0.2534', '0.3682', '-0.4001', '-0.7603', '0.676', '0.1971', '-0.1876', '0.1968', '-0.08386', '-0.5215', '-0.3403', '0.595', '0.0426', '-0.594', '0.4778', '-0.0734', '-0.0715', '-0.02454', '0.3418', '0.3838', '-0.07983', '-0.1907', '-0.292', '-0.6772', '0.06046', '-0.3816', '0.04648', '-0.0333', '0.1711', '0.0823', '-0.1748', '0.191', '-0.1622', '0.841', '-0.2659', '0.902', '-0.1388', '-0.07324', '-0.06635', '-0.1249', '0.2937', '0.269', '-0.3616', '0.1976', '-0.2385']",,,C537934,759.89,,,
mondo:0011309,familial gestational hyperthyroidism,"['hyperthyroidism, familial gestational']",0081102,603373,99819,C1863959,"['-0.3428', '-0.049', '0.1725', '-0.07916', '-0.0471', '-0.066', '0.2291', '0.2766', '-0.03638', '0.10455', '-0.1956', '-0.02461', '-0.09393', '0.12134', '-0.1901', '0.09485', '0.1174', '0.1453', '-0.0488', '-0.462', '-0.01593', '-0.1627', '0.1196', '-0.005386', '0.1338', '0.005604', '0.2563', '-0.1216', '-0.1088', '-0.2466', '0.1827', '0.1498', '0.344', '0.2196', '-0.3662', '-0.05533', '0.0449', '0.2407', '-0.1692', '-0.1614', '0.03885', '0.02943', '0.292', '-0.1484', '0.2168', '-0.3162', '0.02832', '0.2003', '-0.00841', '0.3403', '-0.168', '0.0317', '0.01756', '-0.05005', '-0.165', '0.3232', '0.09454', '-0.4712', '-0.1326', '0.04776', '0.1619', '0.2065', '-0.0892', '-0.3843', '-0.1993', '0.2037', '0.1221', '0.2898', '-0.2311', '0.3735', '-0.1456', '0.204', '0.0541', '-0.257', '0.1376', '0.1129', '0.0832', '-0.0153', '0.10614', '0.04724', '-0.04977', '0.1654', '0.1034', '-0.11444', '0.01074', '0.10077', '0.1268', '0.1146', '0.399', '0.01622', '0.10095', '0.2686', '-0.01582', '-0.1871', '0.476', '0.0803', '0.04044', '-0.3716', '-0.052', '0.2583']",,,C566384,648.10,,,
mondo:0011310,"long chain fatty acids, defect in transport of","['long chain fatty acids, defect in TRANSPORT OF']",,603376,,,,,,,,,,
mondo:0011312,"thyroid carcinoma, nonmedullary, with or without cell oxyphilia","['TCO', 'TCO1', 'nonmedullary thyroid carcinoma, with or without cell oxyphilia', 'thyroid carcinoma, nonmedullary, with or without cell oxyphilia', 'thyroid carcinoma, nonmedullary, with cell oxyphilia', 'TCO 1']",,603386,,C1863925,,,,C537842,,,,
mondo:0011313,megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1,"['PIK3R2 megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome', 'megalencephaly, polymicrogyria, mega corpus callosum syndrome', 'megalencephaly-polymicrogyria-postaxial polydactyly-hydrocephalus syndrome caused by mutation in PIK3R2', 'Meg-PMG-Megacc syndrome', 'megalencephaly, mega corpus callosum, and complete lack of motor development', 'megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 1', 'megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 1', 'MPPH1']",,603387,,,,,,C566381,,,,
mondo:0011314,"Graves disease, susceptibility to, 2","['Graves disease, susceptibility to, type 2', 'Grd2', 'Graves disease, susceptibility to, 2']",,603388,,,,,,,,,,
mondo:0011315,Osebold skeletal dysplasia/osteolysis syndrome,['Osebold skeletal dysplasia/osteolysis syndrome'],,603389,,C1863922,,,,C566380,,,,
mondo:0011316,"osteosclerotic chondrodysplasia, lethal, with intracellular inclusions","['osteosclerotic chondrodysplasia, lethal, with intracellular inclusions']",,603393,,C1863920,,,,C566378,,,,
mondo:0011317,"microcephaly, severe, with skeletal anomalies including posterior rib-Gap defects","['microcephaly, severe, with skeletal anomalies including posterior rib-Gap defects']",,603394,,C1863919,,,,C566377,,,,
mondo:0011318,Tonoki syndrome,"['short stature, brachydactyly, nail dysplasia and mental retardation', 'short stature, brachydactyly, nail dysplasia and intellectual disability', 'Tonoki syndrome']",,603396,,C1863918,,,,C536967,,,,
mondo:0011320,radioulnar synostosis-microcephaly-scoliosis syndrome,"['Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and intellectual disability', 'radioulnar synostosis with microcephaly, short stature, scoliosis, and mental retardation', 'radioulnar synostosis with microcephaly, short stature, scoliosis, and intellectual disability', 'Giuffré-Tsukahara syndrome', 'Tsukahara syndrome', 'Giuffre-Tsukahara syndrome', 'Tsukahara syndrome of radioulnar synostosis, short stature, microcephaly, scoliosis, and mental retardation']",,603438,3268,C1863881,,,,,,,,
mondo:0011321,expansile bone lesions,['expansile bone lesions'],,603439,,C1863880,,,,C566375,,,,
mondo:0011322,"Oroacral syndrome, Verloes-Koulischer type","['Oroacral syndrome, Verloes-Koulischer type']",,603446,,C1863879,,,,C566374,,,,
mondo:0011323,"arhinia, choanal atresia, and microphthalmia","['Bosma arhinia microphthalmia syndrome', 'BOSMA arhinia microphthalmia syndrome', 'arhinia, choanal atresia, microphthalmia, and hypogonadotropic hypogonadism', 'BAMS', 'arhinia, choanal atresia, and microphthalmia']",,603457,1135,,"['-0.04636', '0.05338', '0.04437', '-0.0621', '0.02255', '-0.08466', '0.019', '0.10205', '-0.06055', '-0.06104', '-0.03238', '-0.07245', '-0.05133', '-0.01895', '-0.1415', '-0.05646', '0.03412', '-0.0725', '-0.0265', '-0.2017', '0.02406', '-0.0478', '0.0884', '-0.013504', '0.05685', '0.01743', '-0.0592', '0.05673', '0.08496', '-0.072', '0.06866', '-0.02399', '0.1125', '0.05524', '0.0633', '-0.03067', '-0.01996', '-0.0634', '-0.003035', '-0.1012', '0.0553', '-0.0659', '0.06223', '-0.0801', '-0.01883', '-0.102', '0.002386', '0.0813', '-0.03046', '0.02216', '-0.0814', '-0.04294', '0.03574', '-0.01935', '-0.0757', '-0.03044', '0.0788', '-0.04892', '-0.11755', '0.02231', '0.03546', '0.05466', '-0.014435', '0.03082', '-0.02583', '-0.04016', '0.10846', '0.08215', '-0.0907', '0.1343', '-0.1051', '0.04132', '0.0749', '-0.0858', '0.003056', '-0.04416', '0.0628', '-0.10675', '-0.0935', '-0.04947', '-0.0182', '0.04648', '-0.0171', '0.1173', '-0.0838', '-0.02327', '-0.005295', '0.1287', '0.0576', '0.001743', '0.01743', '0.1256', '0.04037', '0.03165', '0.2126', '-0.009285', '0.083', '-0.1302', '0.06128', '0.0648']",,,C537429,,,,
mondo:0011325,Fanconi anemia complementation group F,"['Fanconi Anemia, complementation group type F', 'Fanconi anaemia complementation group type F', 'Fanconi anemia, complementation group F', 'FANCF', 'Fanconi anemia complementation group type F']",0111088,603467,,,"['-0.4397', '0.3806', '0.01366', '0.4739', '0.743', '0.0504', '-0.2893', '0.4763', '-0.4429', '-0.3538', '0.8203', '0.08417', '0.2996', '0.5356', '-1.083', '0.11115', '-0.595', '0.151', '-0.4788', '-0.402', '-0.06885', '-0.6357', '0.4314', '-0.1566', '0.804', '-0.5635', '0.1324', '-0.4033', '0.6724', '0.0696', '0.2544', '0.117', '0.4734', '0.5444', '0.594', '-0.2073', '-0.997', '-0.6133', '0.5264', '-0.265', '-0.6416', '0.1829', '0.08276', '-0.5303', '-0.654', '-1.045', '0.287', '0.2175', '0.715', '-0.373', '0.526', '0.3994', '0.779', '-0.065', '0.472', '-0.759', '0.2742', '0.5186', '-1.044', '0.1183', '0.00303', '0.457', '-0.297', '-0.4973', '-0.1005', '0.4111', '0.3306', '0.6587', '-0.6626', '0.941', '0.924', '-0.3904', '-0.5938', '-0.58', '0.318', '1.077', '0.1716', '0.4678', '0.04575', '0.4658', '0.1871', '-0.07697', '0.05536', '0.00552', '0.4814', '-0.2363', '-0.5996', '0.412', '0.889', '-0.228', '0.5034', '0.4424', '-0.3748', '-0.09186', '0.6196', '1.049', '0.2352', '-0.1864', '0.218', '-0.4895']",C125707,0009045,,,,,
mondo:0011326,"citrullinemia, type II, adult-onset","['citrullinemia type II', 'citrullinemia, type II, ADULT-onset', 'adult-onset citrullinemia type II', 'CTLN2', 'citrullinemia type 2', 'citrin deficiency', 'adult-onset citrullinemia type 2', 'citrullinemia, adult-onset type II', 'citrullinemia, type II, adult-onset']",0070342,603471,,,,,,,,,,
mondo:0011327,neuronal intranuclear inclusion disease,"['Niid', 'neuronal intranuclear inclusion disease', 'neuronal intranuclear hyaline inclusion disease']",0081294,603472,2289,C1863843,"['-0.739', '-0.1224', '-0.07776', '-0.1129', '-0.375', '-0.85', '-0.3457', '0.346', '-0.6973', '0.0325', '-0.588', '-0.4146', '-0.522', '0.3247', '0.8374', '0.3838', '-0.538', '-0.3525', '-0.6797', '-0.584', '0.5073', '-0.6343', '0.06726', '-0.2202', '0.2817', '-0.1945', '-0.2559', '-0.02885', '-0.5566', '0.3198', '0.3552', '0.2788', '0.359', '-0.1233', '0.4917', '0.02829', '-0.57', '-0.0902', '-0.1849', '0.4258', '-0.0295', '-0.8154', '0.2083', '0.06976', '-0.01269', '-0.6084', '-0.0714', '0.1187', '0.1613', '-0.0433', '-0.04306', '0.659', '-0.5986', '-0.3914', '-0.5293', '-0.1136', '-0.2712', '-0.5376', '-0.1846', '-0.229', '0.1407', '0.1433', '-0.03772', '0.1273', '-0.418', '0.2583', '0.3123', '0.5874', '-0.2275', '0.1257', '0.1642', '-0.4724', '-0.432', '-0.1278', '0.297', '0.1235', '0.1478', '0.377', '-0.0843', '-0.6274', '0.0643', '-1.185', '-0.183', '0.6484', '-0.0717', '0.3901', '-0.008095', '-0.009964', '-0.4287', '-0.01729', '0.309', '-0.254', '-0.2', '0.1846', '0.7017', '0.4265', '0.509', '-0.2357', '0.049', '0.2698']",C122655,,C537395,,,,
mondo:0011330,spinocerebellar ataxia type 10,"['spinocerebellar ataxia 10', 'spinocerebellar ataxia type 10', 'SCA10']",0050960,603516,98761,C4275023,"['0.04495', '-0.1687', '0.0377', '0.1461', '-0.2347', '-0.9297', '0.0901', '0.2102', '-0.723', '-0.9365', '0.0755', '0.3071', '-0.01701', '0.1771', '0.729', '-0.2817', '-0.328', '-0.3708', '0.0791', '-0.71', '-0.1593', '-0.3604', '0.07666', '-0.536', '0.369', '-0.3877', '-0.333', '0.10205', '-0.1299', '-0.7334', '0.10175', '0.285', '-0.4185', '-0.2306', '0.2444', '-0.01516', '0.03265', '0.1974', '0.294', '0.765', '0.4583', '0.05936', '-0.3704', '0.419', '0.4407', '-0.657', '0.1835', '0.2976', '0.5347', '0.10535', '-0.08954', '0.1982', '-0.2039', '-0.4492', '0.0371', '-0.71', '0.3618', '0.3079', '-0.08954', '0.3176', '-0.6753', '0.0974', '0.3494', '-0.192', '-0.3918', '0.4475', '0.2268', '0.438', '-0.5684', '0.52', '0.7944', '0.2251', '0.004555', '-0.5366', '0.7925', '0.537', '0.1586', '0.1951', '0.16', '0.543', '-0.4072', '-0.7866', '0.356', '0.537', '-0.334', '-0.8145', '0.3206', '0.04166', '0.6616', '0.2291', '0.229', '0.5913', '0.0176', '-0.0669', '0.9697', '0.932', '0.3594', '0.389', '-0.2411', '-0.138']",,,C566874,,,,
mondo:0011331,congenital chylothorax,"['chylothorax, congenital', 'hydrothorax, congenital']",0060646,603523,264688,C0340014,,,,C535461,511.89,,,
mondo:0011332,"Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin","['Dyserythropoiesis, congenital, with ultrastructurally normal erythroblast heterochromatin']",,603529,,C3807235,,,,,,,,
mondo:0011334,limb-mammary syndrome,"['limb-mammary syndrome', 'mammary hypoplasia, ectrodactyly, and other hand/foot anomalies', 'LMS']",,603543,69085,,"['0.2241', '0.0462', '0.1609', '0.1014', '0.568', '-0.3347', '-0.00895', '0.02022', '-0.1667', '-0.386', '-0.29', '-0.1139', '-0.0835', '0.096', '0.007717', '0.11835', '-0.01613', '-0.228', '-0.626', '-0.5327', '-0.1011', '0.4668', '0.502', '-0.1805', '0.4377', '0.1561', '-0.2059', '0.328', '0.593', '-0.1316', '0.4053', '-0.07495', '-0.2559', '0.04816', '0.2659', '-0.3562', '-0.355', '0.11255', '-0.11444', '-0.08496', '-0.0106', '-0.2333', '-0.186', '-0.4136', '0.08734', '-0.2922', '0.0302', '0.093', '-0.1283', '-0.443', '0.1516', '-0.3691', '-0.3284', '0.3083', '-0.6885', '-0.3557', '0.551', '-0.1929', '-0.4067', '0.1304', '0.2405', '-0.02623', '-0.05652', '0.1178', '-0.3284', '-0.04565', '0.1094', '0.1334', '-0.3635', '0.10004', '-0.1714', '-0.278', '0.03668', '0.298', '0.2432', '0.1494', '-0.0154', '-0.3025', '-0.301', '-0.4067', '0.1577', '0.2822', '0.6836', '0.4604', '0.0713', '-0.02405', '-0.02202', '0.8965', '0.0823', '0.0638', '0.08203', '0.3018', '0.1815', '-0.1854', '1.033', '0.04178', '0.322', '-0.4343', '0.01779', '0.2634']",,,C535903,,,,
mondo:0011335,spondyloepimetaphyseal dysplasia with multiple dislocations,"['spondyloepimetaphyseal dysplasia with JOINT laxity, type 2', 'spondyloepimetaphyseal dysplasia with joint laxity type 2', 'spondyloepimetaphyseal dysplasia with multiple dislocations, Hall type', 'spondyloepimetaphyseal dysplasia with JOINT laxity type 2', 'spondyloepimetaphyseal dysplasia with joint laxicity, Hall type', 'spondyloepimetaphyseal dysplasia with Joint laxity, leptodactylic type', 'spondyloepimetaphyseal dysplasia with multiple dislocations leptodactylic type', 'SEMDJL2', 'spondyloepimetaphyseal dysplasia with Joint laxity, type 2', 'SEMD-MD', 'spondyloepimetaphyseal dysplasia with Joint laxity, Hall type', 'spondyloepimetaphyseal dysplasia with multiple dislocations Hall type', 'spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type']",0112199,603546,93360,C1863732,"['0.4426', '-0.1599', '-0.1063', '0.2191', '-0.364', '-0.5986', '0.0158', '0.3672', '-1.012', '-0.7866', '0.4038', '0.5576', '0.01723', '0.506', '-0.04242', '0.07', '-0.10535', '-0.4438', '-0.45', '0.11365', '0.532', '0.4358', '0.3594', '0.4028', '-0.4243', '0.305', '-0.386', '-0.387', '-0.11865', '-0.519', '-0.2385', '-0.523', '0.1338', '0.01182', '0.7866', '0.104', '-0.077', '-0.849', '0.4563', '-0.977', '0.1469', '-0.2466', '-0.4473', '0.9766', '-0.1365', '-0.3057', '-0.3103', '0.4622', '0.4429', '-0.12134', '0.132', '-0.4277', '0.9893', '0.1315', '-0.3896', '-0.568', '-0.6587', '-0.2299', '-0.3516', '-0.1575', '0.2197', '0.3643', '-0.7983', '0.2983', '-0.5747', '0.4604', '0.1885', '0.6475', '-0.02216', '0.4785', '-0.05862', '-0.2056', '0.1078', '-0.7544', '0.1656', '-0.10046', '-0.00278', '0.6045', '-0.1779', '-0.4263', '-0.4905', '0.4026', '-0.5103', '1.263', '-0.2651', '0.05624', '0.2102', '0.482', '0.7114', '-0.0699', '-0.00755', '0.6074', '-0.7065', '0.3599', '0.05768', '0.1754', '0.6094', '-0.299', '0.529', '-0.125']",C125419,,C535784,,,,
mondo:0011336,familial hemophagocytic lymphohistiocytosis 4,"['Hlh4', 'HPLH4', 'hemophagocytic lymphohistiocytosis, familial, type 4', 'familial hemophagocytic lymphohistiocytosis type 4', 'HLH4', 'Hplh4', 'hemophagocytic lymphohistiocytosis, familial, 4', 'genetic hemophagocytic lymphohistiocytosis caused by mutation in STX11', 'FHL4', 'STX11 genetic hemophagocytic lymphohistiocytosis']",0110924,603552,540,,,,,C537252,,,,
mondo:0011337,familial hemophagocytic lymphohistiocytosis 2,"['FHL2', 'PRF1 genetic hemophagocytic lymphohistiocytosis', 'hemophagocytic lymphohistiocytosis, familial, type 2', 'HLH2', 'Hplh2', 'familial hemophagocytic lymphohistiocytosis type 2', 'hemophagocytic lymphohistiocytosis, familial, 2', 'HPLH2', 'genetic hemophagocytic lymphohistiocytosis caused by mutation in PRF1', 'Hlh2']",0110922,603553,540,,,,,C537250,,,,
mondo:0011338,Omenn syndrome,"['reticuloendotheliosis familial with eosinophilia', 'Omenn syndrome', 'reticuloendotheliosis, familial, with eosinophilia', 'severe combined immunodeficiency with hypereosinophilia', 'combined immunodeficiency with hypereosinophilia']",0060010,603554,39041,C1801959,"['0.04092', '0.295', '-0.0492', '-0.2408', '0.2058', '-0.4736', '0.3274', '-0.1783', '-0.0498', '-0.6016', '0.2866', '-0.1943', '0.1877', '-0.2478', '-0.6196', '-0.3118', '-0.00826', '-0.464', '0.049', '-1.012', '0.003384', '-0.369', '0.4773', '-0.6113', '0.703', '0.6', '-0.2289', '0.3792', '-0.0962', '-0.4124', '0.3203', '0.2544', '0.4844', '-0.04257', '0.3826', '-0.1699', '0.031', '-0.7334', '-0.6284', '0.0426', '-0.1488', '0.0656', '0.214', '-0.3792', '0.4324', '-0.507', '-0.07965', '-0.644', '-0.0339', '0.413', '-0.0322', '0.03099', '0.5234', '-0.3313', '0.0714', '-0.1073', '0.2449', '-0.000849', '-0.8613', '0.2355', '0.010376', '-0.01129', '0.06537', '0.2415', '0.3245', '0.1432', '0.726', '-0.154', '0.1943', '0.7256', '-0.3857', '-0.689', '-0.0821', '-0.03152', '0.261', '0.2131', '0.5645', '-0.451', '0.478', '0.536', '0.822', '0.2008', '-0.4578', '0.1499', '0.2703', '-0.3564', '0.463', '0.4626', '0.3674', '0.7227', '0.466', '0.01947', '0.0798', '0.4802', '0.1729', '0.5747', '-0.261', '-0.3608', '0.3884', '0.2656']",C61240,,,,,10069097,
mondo:0011339,hereditary spastic paraplegia 8,"['spastic paraplegia 8, autosomal dominant', 'WASHC5 hereditary spastic paraplegia', 'hereditary spastic paraplegia caused by mutation in WASHC5', 'hereditary spastic paraplegia type 8', 'SPG8', 'spastic paraplegia 8', 'autosomal dominant spastic paraplegia 8', 'autosomal dominant spastic paraplegia type 8']",0110823,603563,100989,C1863704,"['-0.2637', '0.1002', '0.1268', '-0.545', '-0.318', '-0.659', '-0.378', '0.11456', '-0.85', '-0.1628', '0.01843', '0.01383', '-0.3015', '0.0788', '0.4595', '-0.1603', '-0.1251', '-0.4124', '-0.02023', '-0.478', '0.1864', '-0.2214', '-0.1342', '0.1697', '0.0649', '0.2067', '0.0935', '0.0891', '-0.23', '-0.1338', '-0.06076', '-0.01979', '0.00817', '0.1191', '-0.2129', '-0.2705', '-0.5034', '-0.03125', '0.010895', '-0.2307', '0.266', '-0.396', '-0.2673', '0.4045', '-0.06335', '-0.2795', '-0.2223', '0.07245', '0.09015', '0.2351', '-0.3838', '0.4392', '-0.191', '-0.2883', '0.2421', '-0.3862', '0.5654', '-0.3376', '-0.315', '0.08514', '-0.1725', '0.1453', '0.51', '0.3015', '-0.4944', '0.346', '0.484', '0.5825', '-0.246', '0.2338', '-0.281', '0.4287', '0.1908', '-0.3025', '0.611', '0.2455', '0.1179', '0.1907', '0.3281', '-0.0792', '0.01424', '-0.289', '0.7705', '0.5356', '-0.05508', '0.11066', '0.02263', '0.2319', '0.398', '0.04617', '0.1443', '0.03001', '0.1059', '0.1064', '0.876', '0.387', '0.5645', '0.2642', '-0.1343', '0.251']",,,C580458,,,,
mondo:0011340,congenital tracheal stenosis,"['tracheobronchial stenosis, congenital']",,603569,141127,,,,,C566362,748.3,,,
mondo:0011341,"microcephaly, facial abnormalities, micromelia, and intellectual disability","['microcephaly, facial abnormalities, micromelia, and mental retardation', 'microcephaly, facial abnormalities, micromelia, and intellectual disability']",,603572,,C1863702,,,,C566361,,,,
mondo:0011342,SLC35A1-congenital disorder of glycosylation,"['carbohydrate deficient glycoprotein syndrome type IIf', 'CMP-sialic acid transporter deficiency', 'CDG IIf', 'congenital disorder of glycosylation type IIf', 'CDG-IIf', 'SLC35A1-CDG', 'CDG2F', 'SLC35A1-CDG (CDG-IIf)', 'congenital disorder of glycosylation type 2f', 'congenital disorder of glycosylation, type IIf', 'CDG syndrome type IIf']",0070258,603585,238459,C1970344,"['-0.3218', '-0.08386', '-0.1059', '-0.2228', '0.02765', '-0.07196', '-0.12445', '-0.0809', '-0.146', '-0.1696', '-0.1902', '-0.1549', '0.0825', '-0.4365', '-0.1857', '-0.1173', '0.03732', '0.0464', '-0.243', '-0.7446', '0.008064', '0.1752', '0.292', '-0.557', '-0.2155', '0.2834', '-0.1483', '0.04752', '0.3447', '-0.419', '-0.05734', '0.3123', '0.695', '0.2761', '-0.3882', '-0.2778', '-0.258', '-0.1768', '-0.188', '-0.4268', '0.1493', '-0.638', '0.3372', '-0.525', '0.1857', '0.266', '-0.2783', '0.083', '-0.03186', '0.3694', '-0.1302', '0.00432', '0.3752', '0.3538', '-0.3472', '-0.527', '-0.03082', '-0.1624', '-0.5293', '0.09216', '0.12054', '-0.202', '0.3567', '-0.4321', '0.0546', '-0.4111', '0.3975', '0.1973', '-0.652', '0.4111', '-0.314', '-0.001181', '-0.0493', '0.1031', '0.05774', '0.1927', '0.11835', '0.1913', '-0.3042', '-0.0844', '-0.2822', '0.1876', '0.1234', '0.356', '0.3884', '0.1891', '0.615', '0.3108', '0.258', '-0.346', '0.2178', '0.412', '-0.171', '0.0835', '0.688', '0.4333', '0.518', '-0.5356', '-0.1075', '0.01788']",,,C567040,,,,
mondo:0011343,"follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts","['follicular atrophoderma, perioral pigmented, with milia and epidermoid cysts']",,603587,,C1863692,,,,C566360,,,,
mondo:0011344,"parotitis, juvenile recurrent","['parotitis, juvenile recurrent']",,603588,,C1863691,,,,C566359,,,,
mondo:0011345,"facial dysmorphism, selective tooth agenesis, and choroid calcification","['facial dysmorphism, selective tooth agenesis, and choroid calcification']",,603589,,C1970343,,,,C567039,,,,
mondo:0011346,xanthinuria type II,"['XDH and AOX dual deficiency', 'xanthinuria type 2', 'type 2 xanthinuria', 'xanthine dehydrogenase and aldehyde oxidase, combined deficiency of', 'type II xanthinuria', 'xanthine dehydrogenase and xanthine aldehyde oxidase dual deficiency', 'XAN2', 'xanthinuria, type II', 'xanthine dehydrogenase and aldehyde oxidase combined deficiency of', 'xanthinuria, type 2']",,603592,93602,C1863688,"['0.00381', '-0.0615', '-0.1677', '-0.2361', '0.05435', '-0.5166', '0.077', '0.1077', '-0.0885', '0.237', '0.1322', '-0.3528', '-0.0708', '0.414', '-0.605', '-0.1816', '0.04953', '0.1376', '0.157', '-0.453', '-0.4497', '-0.06696', '0.754', '-0.1018', '-0.1338', '0.1658', '-0.1626', '-0.1187', '-0.1368', '-0.09216', '0.11914', '0.245', '0.1398', '0.4236', '0.00298', '-0.691', '-0.582', '-0.1556', '-0.2129', '-0.294', '-0.235', '-0.3035', '0.4402', '0.07385', '0.088', '-0.4094', '0.3125', '0.1327', '-0.05713', '0.3442', '0.4346', '-0.2458', '0.2915', '-0.07574', '-0.3364', '-0.4146', '0.5938', '-0.417', '-0.5103', '0.1427', '0.3706', '-0.1349', '0.03546', '-0.3103', '0.2434', '-0.4028', '0.571', '0.407', '-0.1545', '-0.0562', '-0.05377', '-0.12134', '-0.1218', '-0.001916', '0.2776', '0.8325', '-0.0201', '-0.169', '-0.07855', '0.4148', '0.1884', '0.1267', '-0.03024', '0.2429', '0.13', '0.3882', '-0.05725', '-0.623', '0.284', '-0.3462', '0.5566', '0.1765', '-0.0913', '0.05142', '0.9316', '0.863', '0.4204', '-0.1846', '-0.1004', '0.2194']",,,C566358,,,,
mondo:0011347,craniosynostosis with ectopia lentis,['craniosynostosis with ectopia lentis'],,603595,,C1863678,,,,C566357,,,,
mondo:0011348,non-syndromic polydactyly,"['polydactylia', 'nonsyndromic polydactyly (disease)', 'Extra digits', 'supernumerary digits', 'nonsyndromic polydactyly', 'isolated polydactyly']",,,2913,,,,,,,,10036063,
mondo:0011349,"osteoma of cranial vault, familial","['osteoma of cranial vault, familial']",,603600,,C1863677,,,,C566356,,,,
mondo:0011350,autosomal dominant nonsyndromic hearing loss 17,"['DFNA17', 'autosomal dominant nonsyndromic deafness type 17', 'nonsyndromic hereditary deafness DFNA17', 'autosomal dominant nonsyndromic deafness 17', 'late-onset progressive hereditary hearing impairment due to cochleosaccular degeneration', 'autosomal dominant deafness 17', 'cochleosaccular degeneration', 'deafness, autosomal dominant 17', 'deafness, autosomal dominant nonsyndromic sensorineural 17', 'autosomal dominant nonsyndromic deafness caused by mutation in MYH9', 'deafness, autosomal dominant type 17', 'MYH9 autosomal dominant nonsyndromic deafness']",0110548,603622,,,,,,,,,,
mondo:0011351,autosomal recessive nonsyndromic hearing loss 21,"['autosomal recessive nonsyndromic deafness type 21', 'autosomal recessive deafness 21', 'TECTA autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness caused by mutation in tecta', 'DFNB21', 'autosomal recessive nonsyndromic deafness 21', 'deafness, autosomal recessive type 21', 'deafness, autosomal recessive 21', 'tecta autosomal recessive nonsyndromic deafness']",0110479,603629,,C1863655,,,,C566353,,,,
mondo:0011352,"neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia","['neuroendocrine carcinoma of salivary glands, sensorineural hearing loss, and enamel hypoplasia']",,603641,,C1863649,,,,C566352,,,,
mondo:0011353,"atrial septal defect, secundum, with various cardiac and Noncardiac defects","['atrial septal defect, secundum, with various cardiac and Noncardiac defects']",,603642,,C1863648,,,,C566351,,,,
mondo:0011354,situs inversus totalis with cystic dysplasia of kidneys and pancreas,"['situs inversus totalis with cystic dysplasia of kidneys and pancreas', 'situs inversus, cystic dysplastic kidney and pancreas, bowed lower limbs,severe intrauterine growth retardation, and oligohydramnios']",,603643,,C1863647,,,,C536666,,,,
mondo:0011355,cone-rod dystrophy 7,"['RIMS1 cone-rod dystrophy', 'CORD7', 'cone-rod dystrophy caused by mutation in RIMS1', 'cone-rod dystrophy 7', 'cone-rod dystrophy type 7']",0111012,603649,,C1863634,,,,C566350,,,,
mondo:0011356,"exostosis, Dupuytren subungual","['subungual exostoses', 'exostosis, Dupuytren subungual', 'Dupuytren subungual exostosis']",,603656,,C1863622,,,,C535723,,,,
mondo:0011357,eccrine syringofibroadenomatosis with eyelid abnormalities,['eccrine syringofibroadenomatosis with eyelid abnormalities'],,603669,,C1863618,,,,C566347,,,,
mondo:0011358,"blue nevi, familial multiple","['blue nevi, familial multiple']",,603670,,C1863617,,,,C566346,,,,
mondo:0011359,acromelic frontonasal dysostosis,"['AFND', 'Toriello syndrome', 'acromelic frontonasal dysostosis', 'frontonasal dysplasia acromelic', 'acromelic frontonasal dysplasia']",0060342,603671,1827,C1863616,"['-0.3274', '0.02126', '0.8574', '-0.43', '0.4785', '-0.3704', '-0.04117', '0.4375', '-0.6294', '-0.4878', '-0.69', '-0.3245', '0.145', '0.1184', '-0.2551', '-0.2183', '0.291', '-0.753', '-0.2788', '-0.4565', '-0.01221', '0.3623', '0.1439', '-0.05292', '0.2961', '0.0764', '-0.265', '0.08356', '0.714', '-0.546', '0.03955', '-0.734', '0.2502', '0.6094', '0.645', '-0.4087', '-0.3655', '-0.11884', '-0.276', '-0.41', '-0.4197', '-0.3877', '0.01019', '-0.0878', '0.1011', '-0.3142', '-0.01941', '0.7837', '-0.3064', '-0.4883', '-0.0821', '0.2444', '-0.708', '0.0853', '-0.745', '0.05167', '-0.1409', '-0.1497', '-0.6455', '-0.02849', '-0.0812', '0.01668', '-0.4355', '0.3904', '-0.4866', '0.4456', '0.1888', '0.1598', '-0.1438', '0.4258', '-0.2385', '0.2646', '0.373', '0.3623', '-0.2084', '0.5947', '0.3064', '-0.01965', '-0.3066', '-0.503', '-0.1564', '0.2051', '0.0749', '0.6997', '0.0158', '0.0417', '-0.173', '0.775', '0.211', '-0.137', '0.2117', '0.584', '0.671', '0.03143', '0.836', '-0.1737', '0.5054', '-0.423', '0.3591', '0.717']",,,C566345,,,,
mondo:0011360,autosomal recessive nonsyndromic hearing loss 14,"['autosomal recessive nonsyndromic deafness 14', 'deafness, autosomal recessive 14', 'autosomal recessive nonsyndromic deafness type 14', 'DFNB14', 'autosomal recessive deafness 14']",0110469,603678,,C1863613,,,,C566344,,,,
mondo:0011361,prostate cancer/brain cancer susceptibility,"['Pcbc', 'prostate cancer/brain cancer susceptibility', 'prostate cancer/brain cancer susceptibility, somatic', 'Capb']",,603688,,,,,,,,,,
mondo:0011362,"myopathy, myofibrillar, 9, with early respiratory failure","['HIBM-ERF', 'hereditary proximal myopathy with early respiratory failure', 'distal myopathy with early respiratory muscle involvement', 'hereditary inclusion body myopathy with early respiratory failure', 'HMERF-ERF', 'myopathy, proximal, with early respiratory muscle involvement', 'Edström myopathy', 'myopathy, distal, with early respiratory failure, autosomal dominant', 'Edstrom myopathy', 'myofibrillar myopathy with early respiratory failure', 'ADMERF', 'HMERF']",0111188,607569,34521,C4518808,,,,C566343,,,,
mondo:0011363,"diabetes mellitus, noninsulin-dependent, 3","['diabetes mellitus, noninsulin-dependent, 3', 'noninsulin-dependent diabetes mellitus 3', 'diabetes mellitus, noninsulin-dependent, type 3', 'NIDDM3', 'type 2 diabetes mellitus 3']",,603694,,C1863594,,,,C566342,,,,
mondo:0011364,autosomal recessive nonsyndromic hearing loss 16,"['autosomal recessive deafness 16', 'STRC autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive type 16', 'autosomal recessive nonsyndromic deafness 16', 'DFNB16', 'deafness, autosomal recessive 16', 'autosomal recessive nonsyndromic deafness caused by mutation in STRC', 'autosomal recessive nonsyndromic deafness type 16']",0110471,603720,,C1863561,,,,C566339,,,,
mondo:0011365,"blepharophimosis - intellectual disability syndrome, SBBYS type","['SBBYSS', 'Young-Simpson syndrome', 'Ohdo syndrome, SBBYS variant', 'Say-Barber-Biesecker-Young-Simpson syndrome', 'SBBYSS syndrome', 'hypothyroidism-dysmorphism-postaxial polydactyly-intellectual disability syndrome']",0060290,603736,3047,,"['0.413', '-0.03864', '0.2979', '-0.3289', '0.543', '-0.1783', '0.2312', '0.7603', '-1.222', '-0.9795', '-0.2917', '-0.622', '0.1897', '-0.2202', '-0.1225', '-0.1626', '0.1553', '-0.3965', '-0.4448', '-0.9224', '0.4067', '0.1305', '0.4934', '0.0725', '0.289', '-0.00484', '-0.02817', '0.135', '1.2', '-0.708', '0.5713', '-0.386', '0.4172', '0.234', '-0.0006213', '-0.235', '0.1437', '-0.514', '-0.169', '0.3276', '0.2983', '0.2142', '-0.2047', '0.02435', '0.521', '-0.352', '-0.0451', '0.625', '-0.793', '-0.2332', '-0.744', '0.371', '-0.2388', '-0.1484', '-0.9175', '0.2092', '0.2344', '0.3093', '0.01394', '0.266', '-0.007267', '0.7666', '-0.2316', '0.3018', '0.2622', '0.04175', '-0.3186', '0.4014', '-0.397', '-0.1835', '-0.1642', '-0.03732', '-0.1757', '0.02043', '0.3726', '0.236', '-0.0849', '-0.1658', '-0.4067', '0.03668', '0.2952', '-0.01794', '0.2754', '0.9087', '0.1343', '0.8184', '0.207', '0.1685', '-0.0522', '0.3855', '-0.227', '0.299', '-0.00315', '0.1609', '0.482', '0.0801', '0.2688', '-0.204', '0.2559', '0.4653']",,,C536717,759.89,,,
mondo:0011366,ovarian germ cell tumor,"['germ cell tumor of ovary', 'germ cell tumour of ovary', 'ovarian germ cell tumor', 'germ cell neoplasm of ovary', 'ovary germ cell tumour', 'germ cell neoplasm of the ovary', 'ovarian germ cell neoplasm', 'ovarian germ cell cancer', 'ovary germ cell tumor', 'germ cell tumour of the ovary', 'germ cell tumor of the ovary']",2156,603737,,C0238324,,C3873,1000419,,239.5,,,
mondo:0011367,"Acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia","['acrodysplasia with ossification abnormalities, short stature and fibular hypoplasia', 'acrodysplasia with ossification abnormalities, short stature, and fibular hypoplasia']",,603740,,C1863556,,,,C538181,,,,
mondo:0011368,papillary thyroid Microcarcinoma,"['papillary thyroid Microcarcinoma', 'papillary Microcarcinoma of the thyroid', 'papillary thyroid gland Microcarcinoma', 'papillary Microcarcinoma of the thyroid gland', 'thyroid gland papillary Microcarcinoma']",,603744,,C1709457,,C46004,,C563277,,,,
mondo:0011369,"hypercholesterolemia, autosomal dominant, 3","['familial hypercholesterolemia caused by mutation in PCSK9', 'hypercholesterolemia, familial, 3', 'low density lipoprotein cholesterol level quantitative trait locus 1', 'PCSK9 familial hypercholesterolemia', 'Fh3', 'hypercholesterolemia, autosomal dominant, type 3', 'low density lipoprotein cholesterol level QTL 1', 'hypercholesterolemia, autosomal dominant, 3', 'HCHOLA3']",,603776,,C1863551,"['-0.010216', '0.02536', '-0.008545', '-0.01343', '0.02611', '-0.06058', '0.003012', '0.0415', '-0.03308', '-0.02696', '-0.02287', '-0.006046', '8.786e-05', '0.00566', '-0.01878', '-0.01315', '0.004196', '-0.02951', '-0.01729', '-0.0675', '-0.010864', '-0.01746', '0.03116', '-0.01529', '0.01941', '0.00864', '-0.00766', '-0.003475', '0.001336', '-0.0396', '0.03824', '-0.007595', '0.04822', '0.02045', '-0.01248', '-0.0175', '-0.007427', '-0.00821', '0.01118', '-0.03885', '0.01765', '-0.03119', '0.02734', '-0.00511', '-0.0002025', '-0.0391', '-0.01874', '0.01636', '0.01088', '0.01136', '0.0158', '0.00447', '-0.00189', '0.001255', '-0.0163', '-0.02826', '0.03458', '-0.008896', '-0.05438', '0.00678', '0.02095', '0.01726', '0.001619', '0.006844', '-0.0049', '-0.002993', '0.05328', '0.03824', '-0.0368', '0.03406', '-0.02829', '0.006855', '0.011215', '-0.03375', '0.02415', '0.0295', '0.001905', '0.00507', '-0.03552', '-0.02548', '-0.01874', '-0.00967', '0.00432', '0.03876', '0.0007367', '0.0003428', '0.01439', '0.04373', '0.0463', '0.00769', '0.01407', '0.02997', '-0.006702', '0.007103', '0.07916', '0.03156', '0.05225', '-0.05975', '-0.01202', '0.01729']",,,C566337,,,,
mondo:0011370,Stargardt disease 4,"['Stargardt disease type 4', 'PROM1 Stargardt disease', 'STGD4', 'Stargardt disease caused by mutation in PROM1', 'Stargardt disease 4']",,603786,,C1863534,,,,C535521,,,,
mondo:0011371,"hydroa vacciniforme, familial","['hereditary hydroa vacciniforme', 'hydroa vacciniforme, familial', 'familial hydroa vacciniforme']",,603794,,C1863533,,,,C536077,,,,
mondo:0011372,microcephaly with simplified gyral pattern,['microcephaly with simplified gyral pattern'],,603802,,C1863516,,,,C566332,,,,
mondo:0011373,"urinary tract infections, recurrent, susceptibility to","['urinary tract infections, recurrent, susceptibility to']",,603806,,,,,,,,,,
mondo:0011374,"hypercholesterolemia, familial, 4","['familial autosomal recessive hypercholesterolemia', 'hypercholesterolemia, autosomal recessive, 2', 'hypercholesterolemia, autosomal recessive, 1, formerly', 'FHCB2', 'hypercholesterolemia, autosomal recessive', 'hypercholesterolemia, autosomal recessive, 2, formerly', 'ARH', 'FHCB1', 'autosomal recessive hypercholesterolemia 1', 'autosomal recessive hypercholesterolemia 2', 'FHCB1, formerly', 'FHCB2, formerly', 'ARH1', 'ARH2', 'hypercholesterolemia, autosomal recessive, 1']",0090105,603813,,C1863512,,C128114,,C566331,,,,
mondo:0011375,brittle bone disorder,['brittle bone disorder'],,603828,,C1859069,,,,C565842,,,,
mondo:0011376,"ventricular fibrillation, paroxysmal familial, type 1","['ventricular fibrillation during myocardial infarction, susceptibility to', 'IVF', 'ventricular fibrillation, familial, 1', 'ventricular fibrillation, paroxysmal familial, type 1', 'ventricular fibrillation, paroxysmal familial, 1', 'VF1']",,603829,,C2751898,,,,C567851,,,,
mondo:0011377,long QT syndrome 3,"['long QT syndrome caused by mutation in SCN5A', 'SCN5A long QT syndrome', 'LQT3', 'long QT syndrome type 3', 'long QT syndrome 2/3, digenic', 'long QT syndrome 3, acquired, susceptibility to', 'long QT syndrome 3/6, digenic', 'long QT syndrome 3']",0110646,603830,101016,C2931401,"['0.1835', '0.08685', '-0.6626', '0.247', '-0.3748', '-0.217', '0.607', '1.077', '0.0101', '-0.1103', '0.56', '0.2374', '0.262', '0.814', '-0.3896', '0.1375', '-0.773', '-0.1487', '0.0475', '-0.3447', '0.1635', '0.4148', '0.007328', '0.0672', '0.4197', '-0.8237', '0.0857', '0.2576', '0.617', '-0.1243', '0.3313', '0.1782', '0.2092', '0.2047', '-0.775', '-0.2969', '0.1686', '0.3748', '0.003448', '-0.2081', '0.532', '-0.2439', '0.03268', '-0.03494', '0.4058', '-0.431', '-0.9966', '-0.01062', '0.1318', '0.2039', '0.2357', '-0.3174', '-0.09106', '-0.209', '-0.2776', '0.3657', '0.3179', '0.2786', '-0.396', '0.1458', '-0.2507', '0.5083', '0.2306', '-0.362', '-0.7217', '0.3162', '0.09674', '0.0368', '-0.3972', '0.8247', '-0.353', '0.7397', '0.643', '-0.2476', '-0.2244', '0.6187', '0.2288', '-0.003153', '-0.2546', '0.4092', '0.4587', '0.1584', '-0.002552', '-0.1765', '0.3064', '-0.1849', '0.3425', '-0.1825', '0.3513', '0.633', '0.0675', '-0.01436', '0.1492', '-0.138', '0.4414', '0.7524', '1.055', '-0.792', '-0.4287', '-0.0641']",C137959,,C565840,,,,
mondo:0011381,dominant beta-thalassemia,"['beta-thalassemia, dominant inclusion body type', 'inclusion body beta-thalassemia', 'thalassemia-beta, dominant inclusion-body', 'dyserythropoietic Anemia, congenital, Irish or Weatherall type']",0080770,603902,231226,C4274391,"['-0.4312', '0.2449', '-0.09766', '-0.686', '-0.11456', '-0.4634', '-0.9604', '1.4', '-1.05', '-0.9634', '-0.32', '0.10767', '0.327', '0.8223', '-0.292', '0.03604', '-1.333', '-0.4407', '-0.5605', '-0.7563', '-0.4502', '-0.1554', '0.962', '-0.4937', '0.8037', '-0.3047', '0.4294', '-0.1317', '0.4724', '-0.601', '-0.0989', '-0.1422', '0.02925', '-0.5415', '-0.5225', '-0.4739', '-0.8154', '-0.1873', '-0.1619', '-0.8853', '0.3193', '0.3774', '0.5107', '0.06198', '-0.8906', '-0.781', '-0.6465', '-0.876', '0.712', '-0.6855', '0.04483', '-0.8047', '0.4263', '0.1077', '-0.04684', '-0.06635', '-0.4526', '0.875', '-0.205', '0.3235', '-0.308', '-0.2046', '-0.0373', '-0.2343', '-0.569', '-0.03265', '0.1832', '0.91', '-1.134', '0.7173', '0.1581', '0.308', '-0.1488', '-0.03723', '0.522', '0.2142', '-0.282', '0.222', '0.0331', '0.229', '-0.1073', '-0.739', '-0.03943', '-0.33', '-0.4202', '0.164', '0.479', '0.4067', '0.1284', '0.4204', '0.232', '0.1378', '-0.1455', '-0.0978', '0.5947', '0.685', '-0.509', '-0.3635', '-0.01982', '-0.8696']",,,C565834,,,,
mondo:0011382,sickle cell anemia,"['sickle-cell/Hb-C disease without crisis', 'sickle cell disease', 'sickle cell anemia', 'Hb-S/Hb-C disease', 'Hemoglobin S disease', 'Haemoglobin S disease without crisis', 'sickling disorder due to Hemoglobin S', 'hemoglobin SC disease', 'Hemoglobin S disease without crisis', 'drepanocytosis', 'haemoglobin SC disease', 'sickling disorder due to Haemoglobin S', 'HbS disease', 'Haemoglobin S disease', 'Hb SC disease', 'Hb-SS disease without crisis']",10923,603903,232,C0019034,"['-0.367', '-0.3516', '-0.297', '-0.07574', '-0.143', '-0.7637', '-0.11224', '0.4624', '-0.423', '-0.2399', '-0.04633', '-0.0458', '0.03015', '0.4875', '-0.3438', '-0.5396', '-0.53', '-0.010864', '0.137', '0.03363', '-0.716', '0.02617', '0.3926', '0.2888', '-0.396', '-0.4778', '0.08936', '0.7886', '0.386', '0.01994', '0.2101', '-0.3286', '0.3787', '-0.005127', '-0.395', '0.654', '-0.1488', '-0.261', '0.2006', '-0.486', '-0.4604', '-0.0674', '0.2025', '-0.7065', '0.1666', '0.00713', '-0.848', '-0.3674', '0.2961', '0.2313', '-0.2004', '0.12335', '0.2227', '0.3096', '0.5366', '-0.3262', '0.0839', '0.6587', '-0.2808', '-0.02286', '-0.3904', '0.5444', '-0.2247', '0.2349', '-0.1805', '0.094', '0.3376', '0.8784', '-0.4993', '0.2522', '0.549', '0.1416', '-0.3467', '-0.5327', '-0.0008082', '0.2363', '0.1724', '0.0945', '0.2316', '-0.268', '-0.213', '-1.108', '-0.1622', '-0.1027', '-0.06113', '-0.3232', '0.3357', '0.3684', '0.759', '-0.2861', '0.4153', '-0.02379', '-0.3398', '0.2085', '0.3816', '0.883', '-0.4692', '-0.4805', '0.2042', '0.1037']",C34383,1001797,D000755,282.63,,10040641,
mondo:0011383,autoimmune lymphoproliferative syndrome type 2A,"['autoimmune lymphoproliferative syndrome type IIA', 'autoimmune lymphoproliferative syndrome, type II', 'type 2 ALPS', 'autoimmune lymphoproliferative syndrome, type 2', 'type 2 autoimmune lymphoproliferative syndrome', 'autoimmune lymphoproliferative syndrome caused by mutation in CASP10', 'ALPS2A', 'autoimmune lymphoproliferative syndrome-CASP10 variant', 'ALPS-CASP10', 'autoimmune lymphoproliferative syndrome, type IIA', 'CASP10 autoimmune lymphoproliferative syndrome', 'autoimmune lymphoproliferative syndrome, type 2A']",0110115,603909,,C1858968,,C39576,,C565833,,,,
mondo:0011384,"hypertension, essential, susceptibility to, 1","['hypertension, essential, susceptibility to, type 1', 'Hyt1', 'hypertension, essential, susceptibility to, 1']",,603918,,,,,,,,,,
mondo:0011385,intervertebral disk degenerative disorder,"['degenerative disorder of intervertebral disk', 'intervertebral disk degeneration', 'intervertebral Disc Degeneration', 'vertebral disk disease', 'vertebral disc disease', 'lumbar disc degeneration', 'vertebral Disc degenerative disorder', 'intervertebral disc degeneration', 'IDD', 'intervertebral disk degenerative disorder', 'intervertebral Disc degenerative disorder', 'cervical disk degenerative disease', 'degenerative disorder of intervertebral disc', 'lumbar disk degeneration', 'degenerative disk disease', 'intervertebral disk disease', 'intervertebral Disc degenerative disease', 'cervical disc degenerative disease', 'intervertebral disc disease', 'vertebral Disc degenerative disease', 'degenerative disc disease']",90,603932,,C0158266,,C26983,,D055959,722.6,,,
mondo:0011386,"microvascular complications of diabetes, susceptibility to, 1","['microvascular complications of diabetes, susceptibility to', 'microvascular complications of diabetes, susceptibility caused by mutation in VEGFA', 'neuropathy, diabetic, susceptibility to', 'VEGFA microvascular complications of diabetes, susceptibility', 'proliferative retinopathy, diabetic, susceptibility to', 'microvascular complications of diabetes 1', 'nephropathy, diabetic, susceptibility to', 'MVCD1', 'microvascular complications of diabetes, susceptibility to, type 1', 'microvascular complications of diabetes, susceptibility to, 1', 'end-stage renal disease, diabetic, susceptibility to', 'microvascular complications of diabetes, protection against', 'nonproliferative retinopathy, diabetic, susceptibility to']",,603933,,,,,,,,,,
mondo:0011387,"psoriasis 4, susceptibility to","['PSORS4', 'psoriasis 4, susceptibility to', 'psoriasis susceptibility 4']",0111280,603935,,,,,,,,,,
mondo:0011389,autosomal dominant nonsyndromic hearing loss 16,"['autosomal dominant deafness 16', 'autosomal dominant nonsyndromic deafness type 16', 'DFNA16', 'deafness, autosomal dominant 16', 'autosomal dominant nonsyndromic deafness 16']",0110547,603964,,C1858916,,,,C565832,,,,
mondo:0011390,focal segmental glomerulosclerosis 2,"['glomerulosclerosis, focal segmental, 2', 'focal segmental glomerulosclerosis type 2', 'TRPC6 focal segmental glomerulosclerosis', 'focal segmental glomerulosclerosis 2', 'FSGS2', 'focal segmental glomerulosclerosis caused by mutation in TRPC6']",0111129,603965,,C1858915,,,,C565831,,,,
mondo:0011391,megalencephalic leukoencephalopathy with subcortical cysts,"['Van der Knaap syndrome', 'megalencephalic leukoencephalopathy with subcortical cysts 1', 'megalencephaly-cystic leukodystrophy', 'megalencephaly-cystic leukodystrophy syndrome', 'megalencephalic leukoencephalopathy with subcortical cysts type 1', 'MLC1', 'megalencephalic leukodystrophy', 'MLC', 'Vacuolating megalencephalic leukoencephalopathy with subcortical cysts']",0080315,,2478,CN176898,"['-0.1298', '0.1515', '0.2458', '-0.1528', '-0.2952', '-0.4094', '-0.2018', '0.2957', '-0.668', '0.1552', '-0.4766', '0.002672', '-0.1713', '-0.2299', '0.5596', '-0.336', '-0.04633', '-0.3835', '0.1129', '-0.43', '0.12115', '-0.1532', '0.16', '-0.1387', '0.207', '-0.2666', '-0.1145', '-0.02896', '-0.2092', '0.00807', '0.03116', '0.03047', '0.1987', '-0.16', '0.1276', '0.1897', '-0.4585', '-0.09094', '0.1067', '-0.486', '0.3777', '-0.1852', '-0.04236', '0.1823', '-0.0622', '-0.286', '-0.2462', '0.0565', '-0.06934', '0.0337', '0.278', '0.5747', '-0.1255', '-0.012794', '-0.0337', '-0.06186', '0.2988', '-0.11', '-0.286', '0.3774', '-0.10065', '0.4395', '-0.147', '-0.05057', '-0.3206', '-0.0915', '0.2896', '0.4353', '0.1026', '0.437', '-0.15', '0.4565', '0.1849', '-0.2676', '-0.1835', '-0.1006', '0.3887', '-0.08466', '-0.11884', '-0.3962', '-0.3638', '-0.2103', '-0.0889', '0.4346', '-0.02657', '0.09644', '0.0533', '0.2854', '0.251', '0.01678', '0.3018', '0.6074', '0.168', '0.1401', '0.352', '0.241', '0.2932', '0.1858', '0.2935', '0.01746']",,,C536141,,,,
mondo:0011392,autosomal recessive nonsyndromic hearing loss 20,"['deafness, autosomal recessive 20', 'autosomal recessive nonsyndromic deafness 20', 'autosomal recessive nonsyndromic deafness type 20', 'DFNB20', 'autosomal recessive deafness 20']",0110478,604060,,C1858840,,,,C565828,,,,
mondo:0011393,"hypoalphalipoproteinemia, primary, 1","['FHA', 'HDL cholesterol, Low serum', 'HDLD', 'hypoalphalipoproteinemia, primary', 'familial HDL deficiency', 'high density lipoprotein deficiency', 'HDL deficiency, familial, 1', 'hypoalphalipoproteinemia, familial', 'FHD']",0080957,604091,,,,,,,,,,
mondo:0011395,cone-rod dystrophy 3,"['ABCA4 cone-rod dystrophy', 'CORD3', 'cone-rod dystrophy caused by mutation in ABCA4', 'cone-rod dystrophy 3', 'cone-rod dystrophy type 3']",0111013,604116,,C1858806,,,,C565827,,,,
mondo:0011396,loricrin keratoderma,"['Camisa disease', 'keratoderma hereditarium mutilans with ichthyosis', 'keratoderma-ichthyosiform dermatosis-elevated beta-glucuronidase syndrome', 'loricrin keratoderma', 'mutilating keratoderma with ichthyosis', 'Vohwinkel syndrome with ichthyosis', 'Vohwinkel syndrome, variant form']",,604117,79395,C1858805,"['-0.0885', '0.6006', '0.11957', '-0.1638', '-0.01591', '-0.9146', '-0.1157', '-0.0684', '-0.01811', '-0.3777', '-0.2908', '0.11835', '-0.1716', '-0.427', '-0.03845', '0.1321', '0.4155', '-0.4253', '0.1077', '-1.198', '-0.448', '-0.0791', '0.0752', '-0.05847', '0.3474', '0.688', '-0.1576', '0.3281', '-0.1941', '-0.3684', '0.04633', '-0.01245', '-0.2369', '0.2578', '0.1927', '0.03418', '0.00391', '-0.1946', '-0.1617', '-0.5747', '-0.1888', '-0.311', '0.05188', '0.0871', '0.1709', '-0.4822', '-0.673', '0.2961', '-0.0514', '-0.1694', '0.009', '-0.2039', '0.05826', '-0.0769', '-0.2634', '-0.6733', '0.9263', '0.02174', '-0.528', '-0.29', '0.2236', '0.02936', '-0.04694', '-0.0445', '-0.05307', '-0.0357', '0.4866', '0.1892', '-0.1346', '0.738', '-0.65', '-0.1796', '0.3748', '-0.1947', '0.3943', '-0.0731', '0.03326', '-0.0142', '0.1026', '-0.1309', '0.1827', '0.4705', '0.3467', '0.4426', '0.1123', '0.0475', '-0.4685', '0.9834', '0.1406', '0.2847', '0.327', '0.4045', '0.3928', '0.4314', '0.548', '-0.078', '0.628', '-0.9067', '0.2281', '0.1512']",,,C565826,,,,
mondo:0011397,"autosomal dominant cerebellar ataxia, deafness and narcolepsy","['autosomal dominant cerebellar ataxia-deafness-narcolepsy syndrome', 'cerebellar ataxia, deafness, and narcolepsy, autosomal dominant', 'ADCADN', 'ADCA-DN', 'autosomal dominant cerebellar ataxia, deafness, and narcolepsy', 'ADCA-DN syndrome']",0050968,604121,314404,CN203753,"['0.4458', '0.5977', '-0.811', '0.756', '-0.498', '-0.89', '0.3933', '0.878', '0.3677', '-0.5605', '-0.1328', '-0.1211', '-0.3826', '0.482', '-0.06323', '-0.6436', '-0.3452', '-0.2379', '-0.1635', '-0.7656', '-0.2489', '0.2747', '-0.4045', '-0.10205', '-0.528', '-0.55', '0.352', '-0.398', '0.02122', '0.2125', '0.178', '0.04208', '0.2642', '0.003096', '-0.338', '0.04254', '-0.2786', '-0.3218', '0.512', '-0.593', '0.971', '0.2109', '-0.359', '0.4067', '0.1064', '-0.2903', '-0.3542', '0.248', '-0.0346', '0.4214', '0.06573', '0.174', '0.002033', '-0.8716', '0.5986', '0.38', '0.509', '-0.2568', '-0.0998', '-0.3594', '0.04425', '0.1316', '0.03482', '0.1649', '-0.9194', '0.4917', '-0.02173', '-0.0354', '-0.08685', '0.7993', '-0.723', '0.5303', '-0.2075', '-0.5015', '0.2703', '0.579', '-0.6133', '0.5737', '0.1877', '0.3904', '0.5786', '-0.5503', '0.459', '-0.01682', '-0.0863', '0.01118', '0.02213', '0.8643', '0.852', '0.7437', '0.29', '-0.06015', '-0.708', '0.1825', '0.01007', '0.4895', '-0.2888', '-0.6035', '-0.342', '-0.102']",,,,,,,
mondo:0011398,dystrophic epidermolysis bullosa pruriginosa,"['dystrophic epidermolysis bullosa pruriginosa', 'Deb, pruriginosa', 'DEB, pruriginosa', 'epidermolysis bullosa pruriginosa', 'DEB-Pr', 'pruriginous dystrophic epidermolysis bullosa']",,604129,89843,C1275114,"['0.686', '-0.0912', '-0.2734', '0.09235', '0.04276', '-0.6772', '-0.556', '0.4734', '-0.1963', '-0.7754', '0.1168', '-0.4307', '-0.8813', '0.2568', '-0.573', '0.079', '0.158', '-1.06', '-0.2583', '-0.861', '-0.2238', '-0.1597', '0.4321', '0.4937', '0.1765', '0.369', '-1.172', '0.7344', '-0.5044', '-0.778', '0.3022', '-0.3367', '-0.3643', '-0.0823', '0.04346', '0.0897', '-1.173', '0.1776', '1.165', '-0.4565', '0.3257', '-0.7344', '0.1545', '0.04822', '0.0853', '-0.1565', '-0.2015', '0.2233', '0.6074', '-0.01569', '-0.4548', '-0.539', '0.635', '-0.003613', '-0.03114', '-0.5156', '-0.1964', '1.057', '-0.765', '-0.233', '0.1891', '0.3594', '0.04016', '0.1863', '0.941', '0.895', '0.3628', '0.325', '-0.688', '0.2179', '-0.2148', '0.07477', '-0.468', '0.00889', '0.1378', '0.0914', '0.04526', '0.288', '0.1508', '-0.2122', '-0.928', '0.095', '-0.2827', '-0.5063', '0.3333', '0.2051', '-1.016', '0.606', '0.802', '0.5396', '-0.4626', '0.419', '-0.08484', '0.625', '0.09906', '0.729', '0.2384', '-0.5874', '0.7925', '-0.03818']",,,C563192,757.39,,,
mondo:0011399,alpha thalassemia,"['alpha-thalassemia', 'A-thalassemia', 'thalassemia, alpha-', 'thalassemias, alpha-', 'Alpha thalassaemia']",1099,604131,846,C0002312,"['-0.2964', '0.2866', '-0.2411', '-0.602', '0.07306', '-0.6436', '-0.8467', '1.064', '-0.8267', '-0.7354', '-0.1412', '0.2042', '0.4727', '0.5093', '0.014465', '-0.07916', '-1.853', '-0.05054', '-0.539', '-0.5728', '-0.5044', '-0.1399', '1.479', '-0.2009', '0.6377', '-0.02559', '0.533', '-0.3762', '0.6743', '-0.506', '-0.3943', '-0.3176', '-0.1271', '-0.3213', '-0.372', '-0.4116', '-0.7617', '-0.00606', '-0.3696', '-0.8994', '0.07', '0.232', '0.3809', '-0.279', '-0.4163', '-0.5576', '-0.7886', '-0.8403', '0.567', '-0.614', '0.2566', '-0.7676', '0.133', '0.10364', '0.00731', '0.2097', '-0.6714', '0.6494', '-0.142', '0.4204', '-0.3862', '-0.2223', '-0.274', '-0.3208', '-0.36', '0.1161', '0.1667', '0.618', '-0.9746', '0.7983', '-0.01234', '0.3572', '-0.181', '0.04263', '0.6045', '0.1665', '0.1147', '-0.03705', '0.2477', '-0.002523', '-0.12396', '-0.6025', '-0.1963', '-0.1368', '0.05487', '-0.0412', '0.2942', '0.1738', '0.1726', '0.583', '0.4995', '0.1193', '-0.2245', '-0.2205', '0.4648', '0.0764', '-0.407', '-0.3933', '-0.2917', '-0.926']",C34368,,D017085,282.49,D56.0,10043390,
mondo:0011400,dilated cardiomyopathy 1G,"['familial isolated dilated cardiomyopathy caused by mutation in TTN', 'dilated cardiomyopathy type 1G', 'cardiomyopathy, dilated, type 1G', 'cardiomyopathy, dilated, 1G', 'CMD1G', 'TTN familial isolated dilated cardiomyopathy']",0110430,604145,,C1858763,,,,C565824,,,,
mondo:0011401,Alzheimer disease without neurofibrillary tangles,"['Alzheimer disease without neurofibrillary tangles', 'Alzheimer^s disease without neurofibrillary tangles', 'AD15', 'Alzheimer disease-15', 'Alzheimer disease 15', 'Alzheimer^s disease type 15', 'Alzheimer^s disease 15']",0110048,611155,,C1970143,,,,C566998,,,,
mondo:0011402,congenital cataracts-facial dysmorphism-neuropathy syndrome,"['congenital cataracts, facial dysmorphism, and neuropathy', 'cataract, congenital, with Facial Dysmorphism and neuropathy', 'CCFDN']",,604168,48431,C1858726,"['0.01665', '-0.4155', '0.4321', '0.6265', '0.1914', '0.7686', '-0.4202', '0.97', '-0.1583', '-0.7397', '-0.1627', '-0.6006', '0.0161', '1.04', '-0.4136', '0.3423', '0.447', '0.5356', '-0.377', '-0.6455', '0.013374', '0.16', '-0.1562', '-0.2418', '-0.1323', '-0.2493', '-0.1398', '0.1638', '0.3176', '-0.00911', '0.3628', '-0.4705', '0.794', '0.3098', '0.3748', '0.2922', '0.3323', '-1.064', '0.1924', '-0.902', '0.684', '-0.5015', '-0.12384', '0.2812', '0.524', '-0.01511', '0.4238', '-0.0754', '0.7007', '-0.6772', '0.3481', '0.08344', '0.66', '-0.463', '0.351', '-0.3386', '0.6294', '0.3962', '-0.7573', '-0.671', '0.0436', '-0.316', '0.3662', '-0.483', '0.09265', '0.7104', '0.7974', '0.638', '0.4446', '0.6343', '-0.0678', '0.6963', '0.6816', '-0.2404', '1.163', '0.2266', '0.0953', '0.2008', '-0.3008', '0.904', '-0.2527', '0.03748', '-0.775', '0.5044', '-0.2402', '-0.02856', '0.4348', '0.1392', '1.135', '0.3872', '0.1732', '0.3765', '-0.2224', '0.3223', '0.09186', '-0.58', '-0.2155', '-0.3948', '0.1242', '-0.4216']",,,C565822,759.89,,,
mondo:0011403,left ventricular noncompaction 1,"['left ventricular noncompaction 1, with or without congenital heart defects', 'left ventricular noncompaction 1', 'left ventricular noncompaction caused by mutation in DTNA', 'left ventricular noncompaction type 1', 'left ventricular noncompaction 1 with or without congenital heart defects', 'DTNA left ventricular noncompaction', 'LVNC1']",,604169,,C1858725,,,,,,,,
mondo:0011404,Caronte,"['Caronte', 'Car']",,604172,,,,,,,,,,
mondo:0011405,poikiloderma with neutropenia,"['poikiloderma with neutropenia, Clericuzio-type', 'Clericuzio type poikiloderma with neutropenia', 'poikiloderma with neutropenia Clericuzio type', 'poikiloderma with neutropenia', 'poikiloderma with neutropenia, Clericuzio type', 'PN']",0060551,604173,221046,,"['0.2954', '0.3455', '-0.0698', '-0.1714', '0.471', '-0.5317', '0.000461', '0.4207', '-0.3396', '0.3323', '-0.09454', '0.585', '-0.3716', '-0.1704', '-0.01466', '0.1119', '0.693', '-0.2246', '-0.04095', '-0.656', '-0.1849', '-0.1029', '0.1426', '-0.3152', '0.1399', '0.04355', '-0.2847', '0.234', '-0.1783', '-0.577', '0.3892', '0.1112', '-0.0775', '-0.1731', '0.3108', '-0.03204', '-0.4858', '-0.1882', '-0.2676', '-0.075', '-0.3245', '-0.1631', '0.05447', '0.257', '0.01903', '0.0916', '-0.2092', '0.2847', '0.1946', '-0.2354', '-0.4243', '0.2388', '0.5376', '0.3037', '-0.1137', '-0.2051', '0.1876', '0.1597', '-0.1747', '0.2705', '-0.0227', '0.3877', '-0.3528', '-0.1991', '0.4255', '-0.12', '0.515', '0.748', '-0.3008', '0.712', '-0.001963', '-0.539', '0.2527', '-0.03513', '0.10864', '-0.3723', '0.059', '0.4495', '0.402', '-0.5063', '0.1243', '-0.4387', '0.3655', '-0.2046', '-0.2142', '-0.12274', '0.02663', '0.619', '0.452', '0.6846', '0.05383', '0.2236', '0.1605', '-0.1567', '0.262', '0.325', '0.2382', '-0.3782', '-0.04538', '-0.1622']",C177535,,,,,,
mondo:0011406,"cholesteatoma, congenital","['cholesteatoma, congenital']",,604183,,,,,,C562858,,,,
mondo:0011407,"facial paresis, hereditary congenital, 2","['HCFP2', 'Mobius syndrome 3, formerly', 'facial paresis, hereditary congenital, 2', 'Mobius syndrome 3', 'Moebius syndrome 3', 'Moebius syndrome 3, formerly']",,604185,,C1858717,,,,,,,,
mondo:0011408,hereditary spastic paraplegia 10,"['spastic paraplegia 10 with or without peripheral neuropathy', 'SPG10', 'hereditary spastic paraplegia caused by mutation in KIF5A', 'spastic paraplegia 10', 'autosomal dominant spastic paraplegia', 'autosomal dominant spastic paraplegia type 10', 'hereditary spastic paraplegia type 10', 'autosomal dominant spastic paraplegia 10', 'KIF5A hereditary spastic paraplegia', 'spastic paraplegia 10, autosomal dominant']",0110763,604187,100991,C4518536,"['0.0286', '0.33', '-0.12225', '-0.6807', '-0.2632', '-1.022', '-0.4392', '0.1648', '-0.5317', '-0.3987', '0.003523', '0.0825', '0.06195', '0.03796', '0.3813', '-0.3713', '0.0337', '-0.664', '0.2678', '-0.6343', '0.1265', '-0.1432', '-0.02237', '-0.3962', '0.04953', '0.2454', '-0.3428', '0.0417', '-0.0235', '-0.6133', '0.0374', '-0.09515', '-0.1054', '0.4993', '-0.2192', '-0.6157', '-0.4788', '-0.4094', '-0.269', '-0.2164', '0.577', '-0.1781', '-0.1906', '0.1321', '-0.105', '-0.268', '-0.468', '-0.0335', '-0.3245', '-0.010735', '0.09595', '0.466', '-0.1111', '-0.3252', '-0.003872', '-0.6143', '0.6357', '-0.2301', '-0.1621', '0.1346', '-0.3574', '-0.0796', '0.6187', '0.4236', '-0.5166', '0.6416', '0.2742', '0.7124', '-0.372', '0.3955', '-0.2585', '0.6265', '0.3533', '-0.3523', '0.61', '0.1538', '0.008736', '0.06537', '0.2786', '-0.0681', '-0.2952', '-0.0495', '0.4023', '0.9136', '0.168', '0.1348', '-0.02286', '0.387', '0.07385', '0.1556', '0.365', '0.2998', '0.2966', '0.12274', '0.95', '0.1278', '0.4463', '-0.0787', '-0.0686', '0.306']",,,C537482,,,,
mondo:0011409,"hepatic fibrosis, severe, susceptibility to, due to Schistosoma mansoni infection","['Sm2', 'hepatic fibrosis, Severe, susceptibility to, due to Schistosoma japonicum infection', 'hepatic fibrosis, severe, susceptibility to, due to Schistosoma mansoni infection', 'hepatic fibrosis susceptibility due to schistosoma mansoni infection']",,604201,,,,,,,,,,
mondo:0011410,"Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly","['Hirschsprung disease with heart defects, laryngeal anomalies, and preaxial polydactyly']",,604211,,C1858696,,,,C565817,,,,
mondo:0011411,Chudley-McCullough syndrome,"['deafness, autosomal recessive 82, formerly', 'CMCS', 'deafness, autosomal recessive 82', 'deafness, sensorineural, with partial agenesis of the corpus callosum and arachnoid cysts', 'deafness, bilateral sensorineural, and hydrocephalus due to foramen of Monro obstruction', 'Chudley-McCullough syndrome']",,604213,314597,C1858695,"['0.06647', '-0.0621', '0.2827', '-0.2761', '0.2815', '-0.1655', '0.301', '0.2413', '-0.539', '-0.3042', '-0.3816', '-0.3906', '0.04974', '-0.4668', '0.1531', '-0.332', '0.2622', '-0.515', '-0.346', '-0.597', '0.1974', '0.15', '0.2988', '0.00365', '0.524', '-0.03818', '-0.2301', '0.1658', '0.1699', '0.05972', '0.1953', '-0.03732', '0.5664', '-0.0578', '0.08575', '-0.2296', '-0.4883', '-0.1771', '-0.1366', '-0.1886', '0.3376', '-0.02509', '0.1511', '0.1451', '0.16', '-0.5093', '-0.2957', '-0.04376', '0.1599', '-0.1126', '0.2576', '0.10095', '-0.0835', '0.0885', '-0.3137', '0.1534', '0.1793', '-0.2893', '-0.2976', '0.4958', '-0.3398', '-0.005547', '0.2491', '-0.1908', '-0.661', '0.1128', '0.226', '0.501', '-0.287', '0.3528', '-0.3328', '0.3027', '0.1693', '-0.244', '-0.10944', '-0.3633', '0.6465', '0.1719', '-0.2017', '-0.03336', '-0.02159', '-0.014824', '-0.02484', '0.79', '-0.2269', '-0.3364', '0.1549', '0.617', '0.2167', '0.4612', '0.12225', '0.635', '0.2979', '0.12494', '0.3984', '-0.10675', '0.5225', '-0.467', '0.5713', '0.2515']",,,C535459,,,,
mondo:0011412,familial encephalopathy with neuroserpin inclusion bodies,"['encephalopathy, familial, with Collins bodies', 'encephalopathy, familial, with neuroserpin inclusion bodies', 'FENIB']",0050831,604218,85110,C1858680,"['-0.2084', '0.2703', '-0.2297', '-0.3086', '-0.2017', '-0.2715', '-0.1906', '0.2417', '-0.306', '0.01587', '-0.2864', '-0.2211', '0.03122', '0.01457', '0.429', '-0.07996', '-0.0968', '-0.1044', '-0.058', '-0.2678', '0.2888', '-0.127', '0.179', '-0.1104', '0.2637', '-0.05838', '-0.1504', '-0.1779', '-0.1595', '-0.05096', '0.3538', '-0.109', '0.3564', '0.1299', '0.4617', '0.077', '-0.5', '-0.2053', '-0.1506', '-0.4312', '0.345', '-0.5503', '-0.02579', '-0.128', '0.2173', '-0.2883', '-0.1085', '0.0846', '-0.418', '-0.0003338', '0.2334', '0.489', '-0.3274', '-0.06793', '-0.001166', '-0.2607', '0.2278', '-0.276', '-0.11035', '0.08466', '0.2495', '0.1476', '-0.03226', '-0.169', '0.05084', '0.1372', '0.3418', '0.3157', '-0.0592', '0.268', '0.0937', '0.2158', '-0.0542', '-0.02296', '-0.2083', '0.02643', '0.1268', '0.0634', '0.0883', '-0.172', '0.1382', '-0.02559', '-0.07043', '0.342', '-0.01575', '0.04016', '0.05414', '0.3064', '0.275', '0.0731', '0.4475', '0.1353', '-0.10284', '-0.006', '0.3054', '0.136', '0.2815', '-0.0053', '-0.07074', '0.166']",,,C536841,348.39,,,
mondo:0011413,cataract 9 multiple types,"['cataract 9 multiple types with or without microcornea', 'CTRCT9', 'CRYAA cataract (disease)', 'autosomal recessive congenital cataract 1', 'cataract 9, multiple types', 'cataract, autosomal recessive congenital 1', 'cataract, autosomal dominant', 'cataract 9, multiple types, with or without microcornea', 'CATC1']",0110266,604219,98995,C1858679,,,,,,,,
mondo:0011414,Peters anomaly,"['anterior segment dysgenesis 5, multiple subtypes', 'anterior segment dysgenesis 5', 'Peters anomaly (disease)', 'Peters congenital glaucoma', 'ASGD5', 'Peters anomaly']",0080610,604229,708,,"['-0.7603', '0.03293', '0.2292', '0.05707', '0.373', '-0.0707', '-0.186', '0.07886', '-0.344', '-0.2366', '-0.1605', '-0.1521', '-0.1632', '0.00817', '-0.63', '-0.5986', '0.1652', '-0.2096', '0.238', '-0.6333', '-0.003147', '0.04193', '0.286', '0.0758', '0.034', '0.189', '-0.3308', '0.1798', '-0.05432', '0.354', '0.2913', '0.438', '0.2052', '0.197', '-0.04257', '-0.1787', '0.0948', '0.0445', '-0.002523', '-0.537', '0.3218', '-0.2437', '0.2397', '-0.01479', '-0.2185', '-0.07574', '0.2393', '0.0747', '0.163', '0.05634', '0.37', '0.2201', '0.158', '-0.3596', '-0.147', '-0.11835', '0.5894', '-0.01276', '-0.585', '-0.1346', '0.1349', '0.1453', '0.0459', '0.1426', '0.005207', '-0.2241', '0.6357', '0.425', '-0.2484', '-0.0209', '-0.159', '0.1874', '0.2285', '0.05707', '-0.1621', '0.07294', '0.1797', '0.1309', '-0.3237', '-0.1453', '-0.007175', '0.1008', '0.001857', '0.4219', '-0.09186', '-0.5044', '-0.0815', '0.10284', '0.0975', '-0.01206', '0.3972', '0.576', '0.3865', '0.0704', '0.7573', '-0.1523', '0.458', '-0.362', '0.1301', '0.276']",,,C537884,743.44,,10059202,0000659
mondo:0011415,Leber congenital amaurosis 3,"['Leber congenital amaurosis caused by mutation in SPATA7', 'SPATA7 Leber congenital amaurosis', 'retinitis pigmentosa, juvenile, Spata7-related', 'retinitis pigmentosa, juvenile, autosomal recessive', 'amaurosis congenita of Leber, type 3', 'LCA3', 'Leber congenital amaurosis 3', 'Leber congenital amaurosis type 3']",0110331,604232,,,,,,C565814,,H35.5,,
mondo:0011416,"generalized epilepsy with febrile seizures plus, type 1","['GEFSP1', 'generalized epilepsy with febrile seizures plus, type 1', 'Gefs+, type 1']",0111302,604233,,C1858672,,,,C565809,,,,
mondo:0011417,hemochromatosis type 3,"['hereditary hemochromatosis caused by mutation in TFR2', 'hemochromatosis due to defect in transferrin receptor 2', 'TFR2 hereditary hemochromatosis', 'HFE3', 'TFR2-related hemochromatosis', 'hemochromatosis, type 3']",0111030,604250,225123,C1858664,"['0.2903', '0.3115', '-0.684', '0.1272', '0.753', '-0.1383', '-0.6685', '0.5776', '0.267', '0.06024', '0.0651', '0.453', '-0.545', '0.4902', '-0.4565', '-0.1542', '-0.5747', '0.1359', '-0.4768', '-0.7925', '-0.5405', '-0.4233', '0.2281', '-0.3508', '0.317', '0.181', '0.003704', '-0.06223', '0.2705', '0.1566', '0.8584', '-0.699', '0.6265', '0.05405', '-0.1279', '-0.396', '-0.8926', '-0.2925', '0.1831', '0.0517', '0.562', '-0.2164', '-0.00356', '0.57', '0.329', '-1.024', '0.2427', '-0.4956', '-0.12085', '-0.1605', '0.2988', '-0.03687', '0.6377', '0.3914', '0.527', '-0.3076', '0.3706', '0.707', '-0.2734', '-0.2122', '0.325', '0.903', '0.3992', '-0.261', '-0.1669', '0.11426', '-0.2654', '0.6016', '-0.625', '-0.2786', '0.1838', '0.1981', '0.2942', '-0.4023', '0.104', '-0.3643', '-0.1366', '0.8384', '-0.5225', '0.7915', '-0.1487', '-0.3926', '-0.06866', '-0.1223', '0.004303', '-0.7183', '0.8696', '0.3975', '0.5947', '-0.2004', '1.325', '0.4236', '-0.3474', '-0.307', '0.6445', '0.7803', '-0.2673', '-0.382', '-0.373', '0.1414']",,,C537248,,,,
mondo:0011418,"dyslexia, susceptibility to, 3","['dyslexia, susceptibility to, 3', 'DYX3']",,604254,,,,,,,,,,
mondo:0011419,camera-Marugo-Cohen syndrome,"['camera Marugo Cohen syndrome', 'obesity, mental retardation, body asymmetry, and muscle weakness', 'camera-Marugo-Cohen syndrome', 'obesity, intellectual disability, body asymmetry, and muscle weakness']",,604257,,C1858661,,,,C537964,,,,
mondo:0011420,short stature due to partial GHR deficiency,"['GHIP', 'short stature due to partial growth hormone receptor deficiency', 'Growth hormone, insensitivity to, partial', 'Growth hormone deficiency, isolated, partial', 'increased responsiveness to Growth hormone', 'growth hormone insensitivity, partial']",,604271,314802,,"['-0.719', '0.2664', '0.426', '-0.199', '0.1902', '0.05112', '0.1032', '0.3508', '-0.05447', '-0.1349', '0.1119', '0.1594', '-0.005604', '0.01196', '-0.0418', '-0.1504', '0.3513', '0.0548', '-0.3257', '-0.528', '0.003689', '-0.2947', '0.3176', '-0.2294', '0.0205', '0.187', '0.0706', '-0.2109', '-0.09326', '-0.3062', '0.301', '-0.02893', '0.4236', '0.218', '-0.09595', '-0.379', '0.2732', '0.01237', '-0.0751', '-0.177', '0.0707', '-0.1406', '0.2351', '-0.02284', '-0.10944', '-0.3762', '0.2825', '-0.003159', '0.2913', '0.2106', '-0.06104', '-0.3586', '0.04413', '0.2313', '-0.3696', '0.03842', '0.07025', '-0.4988', '-0.418', '0.1771', '0.07117', '0.2139', '-0.002466', '-0.07635', '0.2255', '0.02394', '0.1584', '-0.04843', '-0.2751', '-0.00579', '-0.1865', '-0.03091', '0.2927', '-0.2234', '0.1536', '-0.00598', '0.1543', '0.0703', '-0.1859', '0.0771', '0.08856', '0.1504', '0.03214', '0.1505', '-0.1608', '0.0788', '0.3057', '0.1305', '0.5874', '-0.008766', '-0.03062', '0.3386', '-0.3127', '-0.1665', '0.603', '-0.00297', '0.28', '-0.3914', '0.02678', '0.3838']",,,C565805,,,,
mondo:0011421,"mitochondrial complex V (ATP synthase) deficiency, nuclear type 1","['Complex 5 mitochondrial respiratory chain deficiency', 'ATPAF2 mitochondrial proton-transporting ATP synthase complex deficiency', 'mitochondrial proton-transporting ATP synthase complex deficiency caused by mutation in ATPAF2', 'mitochondrial Complex 5 (ATP synthase) deficiency, nuclear type 1', 'mitochondrial Complex 5 (ATP synthase) deficiency, Atpaf2 type', 'mitochondrial complex V deficiency', 'MC5DN1', 'mitochondrial complex V (ATP synthase) deficiency, nuclear type 1']",0050768,604273,,C3276276,,,,,,,,
mondo:0011422,autosomal recessive proximal renal tubular acidosis,"['renal tubular acidosis, proximal, with ocular abnormalities', 'renal tubular acidosis, proximal, with ocular abnormalities and mental retardation', 'AR pRTA', 'RTA, proximal, autosomal recessive', 'proximal renal tubular acidosis, autosomal recessive', 'proximal renal tubular acidosis with ocular abnormalities and intellectual disability', 'renal tubular acidosis, proximal, with ocular abnormalities and intellectual disability']",,604278,93607,C1970309,"['-0.4597', '0.00932', '0.1952', '-0.4094', '-0.00968', '-0.1438', '-0.2864', '0.6025', '0.04614', '-0.2015', '-0.3374', '-0.513', '-0.2852', '0.393', '-0.3335', '-0.0968', '0.2473', '-0.2389', '0.05542', '-1.1455', '-0.08276', '-0.2505', '0.5054', '0.408', '0.4465', '0.2854', '-0.1873', '-0.0764', '0.1368', '-0.01369', '0.0685', '0.004383', '0.3599', '0.2415', '-0.2015', '-0.1095', '-0.3303', '0.02835', '-0.1703', '-0.1334', '-0.1409', '-0.3025', '0.414', '0.1215', '-0.01688', '-0.2642', '0.1925', '0.00931', '-0.05106', '-0.10175', '0.2766', '0.0806', '-0.2515', '-0.8145', '-0.271', '-0.778', '0.8975', '0.03714', '-0.761', '0.2103', '0.4937', '-0.3909', '0.04767', '-0.2595', '0.1209', '-0.1976', '0.4297', '0.3408', '-0.02357', '0.02275', '-0.663', '0.05234', '0.4329', '0.2086', '0.01697', '0.0684', '0.4558', '-0.29', '-0.2517', '-0.1912', '-0.01646', '0.209', '0.2109', '0.4773', '-0.02112', '0.3494', '0.1887', '-0.3545', '0.4917', '0.08386', '0.413', '0.277', '-0.02437', '0.11914', '0.3374', '0.2554', '0.7705', '-0.09564', '-0.0554', '0.395']",,,C567038,,,,
mondo:0011423,autosomal recessive limb-girdle muscular dystrophy type 2E,"['limb-girdle muscular dystrophy due to beta-sarcoglycan deficiency', 'muscular dystrophy, limb-girdle, autosomal recessive 4', 'SGCB autosomal recessive limb-girdle muscular dystrophy', 'LGMD2E', 'muscular dystrophy limb-girdle with beta-sarcoglycan deficiency', 'Beta-sarcoglycan limb-girdle muscular dystrophy', 'beta-sarcoglycanopathy', 'muscular dystrophy, limb-girdle, type 2E', 'limb-girdle muscular dystrophy type 2E', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCB']",0110279,604286,119,,"['-0.071', '-0.7095', '-0.6597', '-0.4429', '0.4746', '-1.169', '0.1812', '1.042', '-2.014', '-0.9575', '0.1043', '0.5625', '-0.36', '1.141', '0.0182', '0.4333', '-0.8003', '-0.9287', '-0.5767', '-0.753', '0.1847', '0.01255', '0.398', '0.708', '0.3496', '0.1713', '0.0299', '-0.709', '0.2644', '-0.358', '0.792', '-0.04156', '0.5693', '0.1788', '0.0502', '-0.1412', '-0.708', '0.08716', '0.09753', '-0.2522', '0.1625', '-0.192', '-0.3376', '0.5', '-0.3442', '0.4048', '-0.10126', '0.857', '0.0707', '0.6914', '0.1387', '-0.305', '0.3374', '-0.864', '0.2627', '-0.7617', '0.527', '0.8394', '-0.3591', '-0.06125', '0.2493', '-0.04184', '-0.09174', '0.0655', '-0.12415', '0.1691', '0.0002642', '0.5845', '-0.3254', '-0.199', '-0.3208', '0.1389', '0.07043', '0.076', '0.683', '0.3892', '-0.1589', '0.3857', '0.09564', '0.09155', '-0.1731', '-0.1637', '0.10254', '0.10785', '-0.08636', '0.141', '-0.1285', '-0.4226', '0.809', '0.2428', '-0.2576', '-0.1183', '0.307', '0.925', '0.0568', '0.01327', '0.3108', '-0.3362', '-0.1339', '-0.0994']",,,,,,,
mondo:0011424,Carney triad,"['gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma', 'Carney triad']",,604287,139411,C1858592,,C94833,,C565803,,,,
mondo:0011425,dilated cardiomyopathy 1H,"['cardiomyopathy, dilated, with conduction defect', 'CMD1H', 'dilated cardiomyopathy type 1H', 'cardiomyopathy, dilated, 1H', 'dilated cardiomyopathy with conduction defect']",0110429,604288,,C1858591,,,,C536277,,,,
mondo:0011426,aceruloplasminemia,"['hypoceruloplasminemia, hereditary', 'systemic hemosiderosis due to aceruloplasminemia', 'familial apoceruloplasmin deficiency', 'cerebellar ataxia', 'hemosiderosis, systemic, due to aceruloplasminemia', 'hereditary ceruloplasmin deficiency', 'aceruloplasminemia', 'ceruloplasmin deficiency', 'hypoceruloplasminemia']",0050711,604290,48818,,"['-0.2031', '0.63', '0.2568', '-0.2249', '-0.1483', '-0.1257', '-0.10376', '0.0657', '0.01709', '-0.08136', '-0.849', '-0.1101', '0.2031', '-0.314', '0.09607', '-0.1274', '0.0883', '-0.5044', '-0.664', '-0.8955', '-0.0367', '-0.4646', '0.06683', '0.09735', '-0.2517', '-0.0906', '-0.1963', '-0.1611', '-0.7363', '-0.079', '0.591', '0.04837', '0.277', '-0.03983', '0.2057', '-0.01491', '-0.04666', '-0.7393', '-0.12036', '0.1843', '-0.1255', '-0.4043', '0.5723', '0.128', '0.3765', '-0.396', '0.402', '0.4263', '-0.7188', '-0.559', '-0.11664', '0.4717', '0.1259', '0.02563', '0.2878', '-0.05026', '0.6245', '-0.11993', '-0.7896', '-0.02594', '-0.0164', '0.3894', '0.1262', '-0.973', '-0.352', '0.1763', '0.619', '0.02875', '-0.2942', '0.2335', '-0.0929', '-0.431', '-0.4656', '-0.1385', '0.3264', '0.2023', '-0.01437', '-0.3047', '-0.131', '0.2979', '0.2174', '-0.2495', '-0.02727', '0.5547', '0.2185', '-0.1467', '-0.01464', '0.806', '0.5903', '0.1259', '0.345', '0.1641', '0.1171', '-0.1004', '0.555', '0.327', '-0.2083', '0.3816', '0.002216', '0.337']",,,,277.6,,,
mondo:0011427,"Ascaris lumbricoides infection, susceptibility to","['Ascaris lumbricoides infection, susceptibility to', 'ascariasis, susceptibility to']",,604291,,,,,,,,,,
mondo:0011428,"ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3","['EEC syndrome 3', 'ectrodactyly, ectodermal dysplasia, and cleft LIP/palate syndrome 3', 'ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome type 3', 'ectrodactyly, ectodermal dysplasia, and cleft Lip/palate syndrome type 3', 'EEC3', 'EEC syndrome caused by mutation in TP63', 'TP63 EEC syndrome']",0060783,604292,,,,,,C565799,,,,
mondo:0011429,juvenile idiopathic arthritis,"['juvenile chronic polyarthritis', 'acute juvenile rheumatoid arthritis', 'pauciarticular juvenile arthritis', 'pauciarticular onset juvenile chronic arthritis', 'rheumatoid arthritis, systemic juvenile', 'rheumatoid arthritis, systemic juvenile, susceptibility to', 'systemic juvenile rheumatoid arthritis', 'juvenile idiopathic arthritis', 'monarticular juvenile rheumatoid arthritis', 'juvenile rheumatoid arthritis', 'juvenile chronic arthritis', 'Juvenile idiopathic arthritis', 'JIA']",676,604302,92,,,C26979,,D001171,714.33,M08.4,10059177,
mondo:0011430,pulverulent cataract,"['Coppock-like cataract', 'pulverulent cataract', 'dusty cataract']",,,98995,CN207240,"['-0.4695', '0.0604', '0.04883', '0.1109', '0.375', '-0.2448', '-0.2349', '0.2288', '-0.3647', '-0.1572', '-0.1722', '-0.06744', '0.128', '-0.02206', '-0.07184', '-0.04645', '-0.07', '-0.2563', '-0.03065', '-0.3699', '0.01625', '-0.00166', '0.07904', '0.01732', '0.1635', '0.02097', '-0.2448', '0.128', '-0.09033', '0.1289', '0.2255', '0.0881', '0.1827', '-0.004395', '0.1278', '-0.1287', '0.02959', '-0.102', '0.0716', '-0.2303', '0.2021', '-0.1141', '0.0358', '0.0757', '0.000491', '-0.02519', '0.0387', '0.1294', '0.2351', '-0.03217', '0.0644', '-0.1746', '0.1315', '0.1498', '-0.05356', '-0.198', '0.545', '0.0879', '-0.3726', '0.04544', '0.2278', '-0.02281', '0.1975', '0.03198', '-0.03262', '0.0726', '0.3625', '0.2319', '-0.05783', '0.1305', '-0.221', '-0.1476', '0.1748', '-0.02428', '0.0944', '0.02861', '0.02843', '0.1975', '-0.208', '-0.2195', '0.00675', '0.09546', '-0.007217', '0.04474', '-0.1904', '-0.1445', '0.1278', '0.3152', '0.1809', '0.1731', '0.02127', '0.2485', '0.1401', '0.06836', '0.3486', '-0.1732', '0.2805', '-0.4517', '0.1984', '-0.01275']",,,C565133,,,,
mondo:0011431,MASS syndrome,"['OCTD', 'Mitral valve prolapse, Aortic enlargement, Skin and Skeletal findings', 'MASS syndrome', 'overlap connective tissue disease', 'MASS phenotype']",,604308,99715,C1858556,"['-0.00293', '0.002525', '-0.005745', '-0.011024', '0.013214', '-0.01113', '-0.005703', '0.004078', '-0.012344', '-0.01372', '0.003426', '-0.005966', '0.00497', '0.01041', '-0.003187', '-0.004795', '0.00413', '-0.00504', '-0.01196', '-0.02034', '0.001881', '0.0009427', '0.003637', '-0.00512', '-0.00498', '0.00429', '0.006', '-0.00526', '-0.00959', '0.005573', '0.0108', '-0.00712', '-0.0004864', '0.00679', '0.00575', '-0.00503', '-0.00932', '0.003836', '0.000927', '-0.01287', '0.001062', '0.002504', '0.001352', '-0.01039', '0.01014', '-0.01155', '0.004925', '0.003859', '0.003721', '0.003439', '0.00354', '0.003029', '0.000839', '0.007214', '0.00486', '0.003708', '0.000842', '-0.00746', '-0.00932', '0.002707', '0.003914', '0.00865', '-0.00804', '-0.005104', '-0.01203', '-0.002253', '0.0152', '0.00536', '-0.005287', '0.00502', '-0.005047', '0.005875', '-0.00011617', '-0.00526', '0.005974', '0.00416', '-0.00707', '0.001673', '-0.001493', '-0.01092', '0.003742', '0.006626', '-0.0003748', '0.011444', '0.0047', '0.003227', '0.01154', '0.01193', '-0.000444', '0.00438', '-0.00256', '0.006924', '-1e-07', '0.012405', '0.01204', '0.00657', '0.0007424', '-0.01455', '-0.010315', '0.00787']",,,C536030,,,,
mondo:0011432,"blepharophimosis - intellectual disability syndrome, Verloes type","['blepharophimosis with facial and genital anomalies and intellectual disability', 'BMRS, Verloes type', 'blepharophimosis with facial and genital anomalies and mental retardation', 'BMRS type V', 'blepharophimosis-mental retardation syndrome, Verloes type', 'blepharophimosis-intellectual disability syndrome type V', 'blepharophimosis-intellectual disability syndrome, Verloes type']",,604314,293725,C1858538,,,,C565797,,,,
mondo:0011433,"anemia, congenital hypoplastic, with multiple congenital anomalies/intellectual disability syndrome","['anemia, congenital hypoplastic, with multiple congenital anomalies/mental retardation syndrome', 'anemia, congenital hypoplastic, with multiple congenital anomalies/intellectual disability syndrome']",,604315,,C1858537,,,,C565796,,,,
mondo:0011434,"psoriasis 5, susceptibility to","['psoriasis 5, susceptibility to', 'PSORS5', 'psoriasis susceptibility 5']",0111282,604316,,,,,,,,,,
mondo:0011435,"microcephaly 2, primary, autosomal recessive, with or without cortical malformations","['microcephaly 2, primary, autosomal recessive, with or without cortical malformations', 'MCPH2']",0070293,604317,,C1858535,,,,C565794,,,,
mondo:0011436,autosomal recessive distal spinal muscular atrophy 1,"['distal-HMN type 6', 'HMN VI', 'neuronopathy, distal hereditary motor, type VI', 'Hmn6', 'autosomal recessive spinal muscular atrophy with respiratory distress', 'severe infantile axonal neuropathy with respiratory failure', 'autosomal recessive distal spinal muscular atrophy type 1', 'spinal muscular atrophy, distal, autosomal recessive, type 1', 'neuronopathy, distal hereditary motor, type 6', 'neuronopathy, Severe infantile axonal, with respiratory failure', 'DSMA1', 'dSMA1', 'spinal muscular atrophy caused by mutation in IGHMBP2', 'spinal muscular atrophy with respiratory distress 1', 'SMARD1', 'SIANRF', 'diaphragmatic spinal muscular atrophy', 'spinal muscular atrophy, diaphragmatic', 'distal hereditary motor neuropathy type 6', 'severe infantile axonal neuropathy with respiratory failure type 1', 'HMN 6', 'spinal muscular atrophy with respiratory distress type 1', 'IGHMBP2 spinal muscular atrophy', 'spinal muscular atrophy, distal, autosomal recessive, 1', 'dHMN6']",0111064,604320,98920,C1858517,"['-0.377', '-0.0748', '0.08215', '-0.3982', '-0.1653', '-0.6406', '0.1116', '0.8164', '-0.6943', '-0.2087', '-0.1774', '-0.2231', '-0.2216', '-0.00911', '0.04465', '-0.0637', '0.4185', '-0.099', '-0.1672', '-0.7554', '0.2993', '-0.355', '0.2476', '-0.02173', '-0.09814', '-0.077', '0.3818', '-0.2085', '-0.3374', '-0.3906', '0.2463', '0.2029', '0.2651', '0.258', '-0.313', '-0.12036', '-0.1307', '0.2', '-0.1126', '-0.1829', '-0.3516', '0.03235', '-0.3323', '0.6626', '-0.482', '-0.04608', '-0.1292', '0.275', '0.1089', '0.6475', '-0.2019', '0.2163', '0.09595', '-0.3525', '-0.1553', '-0.3623', '-0.0002582', '-0.1411', '0.1163', '0.265', '-0.251', '0.1987', '-0.4226', '-0.1808', '-0.528', '0.1196', '0.2325', '0.5', '-0.5293', '0.4202', '-0.2134', '0.334', '0.05374', '-0.5347', '-0.03964', '-0.04068', '0.4692', '0.3782', '-0.1677', '0.01521', '0.0869', '-0.1642', '0.5225', '0.3486', '-0.4568', '0.09143', '0.09045', '0.2676', '0.3857', '-0.1042', '0.2527', '-0.06805', '0.1589', '0.241', '0.339', '0.4824', '0.3928', '0.218', '-0.05957', '0.3914']",,,C536880,335.19,,,
mondo:0011437,"microcephaly 4, primary, autosomal recessive","['MCPH4', 'microcephaly 4, primary, autosomal recessive']",0070291,604321,,C1858516,,,,C565792,,,,
mondo:0011438,acne,"['acne', 'acne varioliformis', 'acne, adult', 'acne (disease)', 'acne vulgaris', 'frontalis acne']",6543,,,,,C27195,0003894,,706.0,,,0001061
mondo:0011439,spinocerebellar ataxia type 12,"['spinocerebellar ataxia type 12', 'SCA12', 'spinocerebellar ataxia 12']",0050962,604326,98762,C4304885,"['-0.0772', '-0.2103', '-0.1161', '0.1581', '-0.2666', '-1.064', '0.2617', '0.2252', '-0.467', '-0.806', '-0.01979', '0.2683', '-0.0971', '0.07697', '0.6333', '-0.4036', '-0.1593', '-0.3171', '0.2354', '-0.813', '-0.2146', '-0.4153', '0.2046', '-0.4917', '0.2445', '-0.2145', '-0.4146', '0.1849', '-0.2264', '-0.821', '0.226', '0.2227', '-0.4846', '-0.3564', '0.3328', '-0.03091', '-0.1182', '0.06384', '0.3506', '0.486', '0.3938', '0.1727', '-0.297', '0.4104', '0.512', '-0.653', '0.08405', '0.492', '0.3516', '-0.1111', '-0.0658', '0.1578', '-0.01823', '-0.553', '-0.1157', '-0.6675', '0.1909', '0.392', '-0.093', '0.3953', '-0.5435', '0.3235', '0.2168', '-0.1605', '-0.4783', '0.5137', '0.289', '0.5913', '-0.56', '0.539', '0.8286', '0.444', '-0.02705', '-0.7695', '0.676', '0.2522', '0.3274', '0.2983', '0.1038', '0.6465', '-0.4297', '-0.9805', '0.5234', '0.575', '-0.236', '-0.66', '0.2678', '0.06757', '0.6616', '0.3994', '0.4236', '0.5654', '-0.05582', '-0.198', '1.028', '0.831', '0.493', '0.4792', '-0.1493', '-0.0798']",C154316,,C565790,,,,
mondo:0011440,"hypertension, essential, susceptibility to, 2","['hypertension, essential, susceptibility to, type 2', 'Hyt2', 'hypertension, essential, susceptibility to, 2']",,604329,,,,,,,,,,
mondo:0011441,complex regional pain syndrome type 1,"['CRPS1', 'reflex neurovascular dystrophy', 'CRPS I', 'RND', 'complex regional pain syndrome type 1', 'Complex regional pain syndrome I', 'RSDS', 'reflex sympathetic dystrophy', 'reflex sympathetic dystrophy syndrome', 'Algodystrophy']",1811,604335,99995,C0034931,,C85042,1001147,D012019,733.7,M89.0,10064334,
mondo:0011442,advanced sleep phase syndrome 1,"['familial advanced sleep phase syndrome 1', 'advanced sleep phase syndrome, familial, 1', 'FASPS1', 'advanced sleep phase syndrome type 1', 'PER2 advanced sleep phase syndrome', 'advanced sleep phase syndrome, familial, type 1', 'advanced sleep phase syndrome caused by mutation in PER2']",0110011,604348,,C3807327,,,,,,,,
mondo:0011443,"febrile seizures, familial, 4","['FEB4', 'convulsions, familial febrile, 4', 'febrile seizures, familial caused by mutation in ADGRV1', 'ADGRV1 febrile seizures, familial', 'febrile seizures, familial, type 4', 'febrile seizures, familial, 4']",0111305,604352,,C1858493,,,,C565788,,,,
mondo:0011444,Duane retraction syndrome 2,"['Duane syndrome type 2', 'DURS2', 'Duane retraction syndrome caused by mutation in CHN1', 'CHN1 Duane retraction syndrome', 'Duane retraction syndrome 2', 'Duane retraction syndrome type 2']",,604356,,,,,,,,,,
mondo:0011445,hereditary spastic paraplegia 11,"['hereditary spastic paraplegia caused by mutation in SPG11', 'spastic paraplegia 11', 'spastic paraplegia - intellectual deficit - thin corpus callosum', 'Nakamura-Osame syndrome', 'Nakamura Osame syndrome', 'autosomal recessive spastic paraplegia 11', 'hereditary spastic paraplegia type 11', 'spastic paraplegia-intellectual disability-thin corpus callosum syndrome', 'SPG11 hereditary spastic paraplegia', 'autosomal recessive spastic paraplegia complicated with thin corpus callosum', 'hereditary spastic paraplegia mental impairment and thin corpus callosum', 'spastic paraplegia, autosomal recessive, complicated, with thin corpus callosum', 'SPG11', 'autosomal recessive spastic paraplegia with mental impairment and thin corpus callosum', 'spastic paraplegia, autosomal recessive, with mental impairment and thin corpus callosum', 'HSP-TCC', 'spastic paraplegia 11, autosomal recessive', 'autosomal recessive spastic paraplegia type 11']",0110764,604360,2822,,"['-0.3586', '0.1954', '0.1885', '-0.4587', '-0.2742', '-0.6104', '-0.3647', '0.2393', '-0.8687', '-0.0865', '-0.2966', '-0.3452', '-0.0699', '-0.2803', '0.6743', '-0.3013', '-0.10956', '-0.1783', '-0.0431', '-0.3267', '0.401', '-0.1829', '0.09705', '0.04968', '0.06934', '0.11975', '0.0815', '0.1216', '-0.04565', '-0.239', '0.03044', '0.05698', '0.284', '-0.1825', '0.1462', '-0.0625', '-0.2192', '-0.3464', '0.1272', '-0.326', '0.25', '-0.7715', '-0.1196', '0.322', '-0.303', '-0.4429', '-0.0595', '0.02739', '0.158', '-0.1036', '0.12085', '0.4622', '-0.4836', '-0.03622', '-0.1642', '-0.267', '0.3633', '-0.1697', '-0.2355', '0.332', '-0.5957', '-0.003881', '0.2568', '0.1511', '-0.4622', '0.3196', '0.3064', '0.501', '-0.2244', '0.4622', '-0.29', '0.2776', '0.1532', '-0.3994', '0.2576', '0.2198', '-0.114', '-0.0495', '0.000639', '-0.0807', '-0.1025', '-0.2104', '0.382', '0.7905', '-0.1759', '0.0867', '0.01163', '0.4785', '0.428', '-0.03772', '0.2225', '-0.0618', '0.1428', '0.1302', '0.5283', '0.3223', '0.5654', '0.03934', '0.16', '0.4138']",C148317,,,,,,
mondo:0011446,"myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders","['myoclonic epilepsy, congenital deafness, macular dystrophy, and psychiatric disorders']",,604363,,C1858478,,,,C565786,,,,
mondo:0011448,PPARG-related familial partial lipodystrophy,"['PPARG-related FPLD', 'familial partial lipodystrophy associated with PPARG mutations', 'lipodystrophy, familial partial, type 3', 'FPLD3', 'insulin resistance, severe, digenic', 'familial partial lipodystrophy type 3', 'lipodystrophy, familial partial, associated with Pparg mutations']",0070204,604367,79083,,"['-0.1592', '0.3115', '0.2664', '-0.398', '0.2333', '-0.487', '0.01727', '0.1202', '-0.4026', '-0.1092', '-0.608', '-0.154', '0.01744', '-0.02345', '-0.3706', '-0.1665', '0.2834', '-0.1854', '0.002798', '-0.3037', '0.003323', '-0.4458', '0.2482', '0.2532', '-0.1256', '0.4026', '0.1302', '-0.08765', '0.1178', '-0.2778', '0.836', '0.0659', '0.393', '-0.10284', '0.2472', '-0.157', '-0.0728', '-0.1017', '-0.06223', '-0.3604', '-0.3672', '-0.3992', '0.34', '0.5396', '-0.04532', '-0.03952', '0.1819', '0.2211', '0.03397', '-0.07526', '-0.2925', '0.3228', '0.2129', '0.1049', '-0.3914', '-0.2408', '0.2834', '-0.4905', '-0.3064', '0.1454', '0.02846', '0.1675', '-0.1271', '-0.5054', '-0.0377', '0.1836', '0.1348', '0.1646', '-0.02902', '0.1409', '-0.2075', '0.01527', '0.2228', '0.1442', '0.198', '-0.02548', '0.1846', '0.2063', '0.03833', '-0.07025', '-0.0716', '0.2737', '0.1449', '-0.0762', '-0.06537', '0.1604', '0.01317', '0.2444', '0.5044', '0.1494', '0.0762', '0.04138', '0.2384', '-0.1881', '0.5938', '-0.2654', '0.503', '-0.2703', '-0.2102', '0.1581']",,,,,,,
mondo:0011449,Salla disease,"['sialuria, Finnish type', 'Salla disease', 'sialic acid storage disease', 'SD']",,604369,309334,C1096903,"['-0.0502', '0.779', '0.324', '-0.198', '-0.2717', '-0.7173', '-0.1561', '0.4756', '-0.8896', '-0.274', '-0.26', '-0.0653', '0.0768', '0.2391', '0.461', '0.1648', '-0.1476', '-0.2812', '-0.587', '-0.4338', '0.2365', '-0.302', '0.05472', '-0.0783', '-0.05978', '-0.3071', '-0.10986', '0.05362', '-0.4617', '0.1206', '0.29', '0.2969', '0.574', '-0.0911', '-0.05835', '0.04376', '-0.08563', '-0.2151', '-0.2313', '0.4382', '-0.12213', '-0.3157', '0.03607', '0.3022', '-0.00375', '-0.1578', '0.238', '0.0601', '0.0301', '0.265', '-0.3464', '0.2627', '-0.11926', '-0.378', '0.167', '-0.278', '0.2272', '0.7236', '-0.316', '0.1252', '-0.01643', '0.258', '0.4321', '0.02214', '-0.2644', '-0.0778', '0.3005', '-0.1398', '-0.2947', '-0.03693', '-0.1644', '-0.3347', '0.05023', '-0.1848', '0.2786', '0.3613', '0.1475', '0.2644', '-0.1162', '0.202', '0.277', '-0.5', '-0.1873', '0.2203', '0.1431', '0.1768', '-0.1443', '-0.0378', '0.298', '0.637', '0.06354', '0.1754', '0.07855', '0.06744', '0.406', '0.609', '0.1982', '-0.3333', '0.6016', '0.3652']",C85067,,,,,10067531,
mondo:0011450,"breast-ovarian cancer, familial, susceptibility to, 1","['breast cancer, familial, susceptibility to, 1', 'hereditary breast ovarian cancer syndrome caused by mutation in BRCA1', 'breast-ovarian cancer, familial, susceptibility to, 1', 'susceptibility to familial breast-ovarian cancer 1', 'BRCA1 hereditary breast ovarian cancer syndrome', 'breast-ovarian cancer, familial, 1, multifactorial', 'breast-ovarian cancer, familial, susceptibility to, type 1', 'BROVCA1', 'ovarian cancer, familial, susceptibility to, 1']",,604370,,,,,,,,,,
mondo:0011451,"cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1","['SCO2 fatal infantile encephalocardiomyopathy', 'mitochondrial complex IV deficiency, nuclear type 2', 'cytochrome C oxidase deficiency, fatal infantile, with cardioencephalomyopathy', 'fatal infantile encephalocardiomyopathy caused by mutation in SCO2', 'CEMCOX1', 'cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1', 'cardioencephalomyopathy, fatal infantile, due to cytochrome C oxidase deficiency type 1']",0080357,604377,,,,,,,,,,
mondo:0011452,hypotrichosis 7,"['hypotrichosis caused by mutation in LIPH', 'LIPH hypotrichosis', 'hypotrichosis, localized, autosomal recessive 2', 'woolly hair, autosomal recessive 2 with or without hypotrichosis', 'alopecia universalis congenita, Mari type', 'total Mari type hypotrichosis,', 'wooly hair, autosomal recessive 2, with or without hypotrichosis', 'hypotrichosis 7', 'hypotrichosis, autosomal recessive', 'wooly hair, autosomal recessive 2 with or without hypotrichosis', 'HYPT7', 'Wh/Ht', 'hypotrichosis type 7', 'total hypotrichosis, Mari type', 'woolly hair, autosomal recessive 2, with or without hypotrichosis', 'Mari type alopecia universalis congenita', 'Lah2', 'hypotrichosis, total, Mari type']",0110704,604379,,,"['-0.1078', '0.2253', '-0.0563', '-0.0779', '0.1564', '-0.3213', '-0.0494', '0.1655', '-0.1997', '-0.1632', '-0.06238', '-0.01857', '-0.1222', '-0.002838', '0.03683', '-0.06433', '0.1602', '-0.1365', '-0.1061', '-0.341', '-0.08514', '-0.0563', '0.0927', '0.01384', '0.1682', '0.12305', '-0.0808', '0.0669', '0.0397', '-0.1528', '0.2018', '0.01378', '0.05203', '0.07983', '0.0903', '-0.07495', '-0.09186', '-0.11', '0.04822', '-0.1636', '0.1794', '-0.1406', '0.11224', '0.02249', '-0.05084', '-0.2578', '0.006615', '0.0862', '0.106', '-0.127', '0.003172', '-0.1076', '0.1294', '0.03204', '-0.122', '-0.2297', '0.2974', '-0.02863', '-0.3171', '-0.12006', '0.0768', '0.11005', '0.1627', '-0.077', '0.11395', '0.1963', '0.187', '0.02856', '-0.1759', '0.254', '-0.281', '-0.1415', '0.10297', '-0.1126', '0.1282', '0.006783', '0.02162', '-0.01988', '-0.06305', '-0.0422', '0.11017', '-0.0548', '0.06085', '0.0447', '0.03308', '-0.1534', '0.08923', '0.2479', '0.2224', '0.2212', '0.0861', '0.1572', '0.11536', '0.01373', '0.505', '0.05978', '0.2004', '-0.317', '0.06555', '0.06204']",,0009163,C536973,,,,
mondo:0011453,ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia,['ulnar ray dysgenesis with postaxial polydactyly and renal cystic dysplasia'],,604380,,C1858422,,,,C565783,,,,
mondo:0011454,patent ductus arteriosus-bicuspid aortic valve-hand anomalies syndrome,"['patent arterial duct-bicuspid aortic valve-hand anomalies syndrome', 'patent ductus arteriosus and bicuspid aortic valve with hand anomalies']",,604381,228190,C1858420,,,,C565782,,,,
mondo:0011455,"lissencephaly, familial, with cleft palate and cerebellar hypoplasia","['lissencephaly, familial, with cleft palate and cerebellar hypoplasia']",,604382,,C1858419,,,,C565781,,,,
mondo:0011456,nephronophthisis 3,"['nephronophthisis type 3', 'NPHP3 nephronophthisis (disease)', 'NPH3', 'nephronophthisis 3', 'Nph3', 'NPHP3']",0111114,604387,,C1858392,,,,C565780,,,,
mondo:0011457,ataxia-telangiectasia-like disorder,"['ataxia - telangiectasia-like disorder', 'ataxia-telangiectasia-like disorder 1', 'ataxia-telangiectasia-like disorder type 1', 'ATLD', 'ATLD1']",,,,CN239583,,,,C565779,334.8,,,
mondo:0011458,Leber congenital amaurosis 4,"['cone-rod dystrophy', 'Leber congenital amaurosis 4', 'LCA4', 'Leber congenital amaurosis type 4', 'retinitis pigmentosa, juvenile, Aipl1-related', 'Leber congenital amaurosis caused by mutation in AIPL1', 'retinitis pigmentosa, juvenile', 'amaurosis congenita of Leber, type 4', 'AIPL1 Leber congenital amaurosis', 'cone-rod dystrophy, Aipl1-related']",0110332,604393,791,C1858386,"['-0.4731', '-0.05124', '-0.3884', '0.4756', '-0.0668', '-0.04794', '-0.3345', '0.632', '-0.767', '-0.2527', '-0.4646', '-0.1186', '-0.4705', '0.1967', '0.2435', '-0.339', '0.03714', '0.2366', '0.5264', '-0.721', '-0.3967', '-0.4192', '-0.0632', '-0.02335', '-0.1242', '0.06128', '-0.2917', '0.319', '-0.5986', '0.568', '0.9297', '-0.4812', '-0.2896', '0.266', '-0.0595', '0.0788', '0.4375', '-0.734', '0.2391', '-0.2406', '-0.03427', '-0.4424', '0.3853', '-0.3416', '-0.4111', '-0.2751', '-0.1055', '-0.6016', '0.1388', '0.573', '0.777', '0.4038', '0.55', '-0.819', '0.3057', '0.012596', '0.9604', '-0.001182', '-0.656', '0.04666', '-0.0972', '-0.3677', '0.1632', '-0.11194', '-0.4802', '-0.18', '0.517', '0.9087', '0.1436', '0.3823', '0.04977', '-0.385', '0.03775', '-0.05203', '0.505', '-0.2386', '0.1538', '-0.05997', '0.02818', '-0.2426', '0.2358', '-0.1849', '-0.389', '0.873', '-0.3142', '0.10803', '0.10736', '-0.12384', '0.10236', '0.05594', '0.4504', '0.2268', '-0.1049', '0.1758', '0.6147', '-0.1301', '0.2247', '-0.3904', '0.161', '-0.007698']",,,C565778,,H35.5,,
mondo:0011459,arrhythmogenic right ventricular dysplasia 5,"['ARVC5', 'ARVD5', 'arrhythmogenic right ventricular dysplasia, familial, 5', 'TMEM43 arrhythmogenic right ventricular cardiomyopathy', 'arrhythmogenic right ventricular cardiomyopathy 5', 'arrhythmogenic right ventricular dysplasia type 5', 'familial arrhythmogenic right ventricular dysplasia 5', 'arrhythmogenic right ventricular cardiomyopathy caused by mutation in TMEM43', 'arrhythmogenic right ventricular dysplasia, familial, type 5']",0110074,604400,,C1858379,,,,C565776,,,,
mondo:0011460,arrhythmogenic right ventricular dysplasia 6,"['ARVD6', 'familial arrhythmogenic right ventricular dysplasia 6', 'arrhythmogenic right ventricular dysplasia, familial, 6', 'arrhythmogenic right ventricular dysplasia type 6', 'arrhythmogenic right ventricular cardiomyopathy 6', 'ARVC6']",0110075,604401,,C1858378,,,,C565775,,,,
mondo:0011461,"generalized epilepsy with febrile seizures plus, type 2","['febrile seizures, familial caused by mutation in SCN1A', 'generalized epilepsy with febrile seizures plus, type 2', 'SCN1A febrile seizures, familial', 'febrile seizures, familial, 3A', 'Gefs+, type 2', 'GEFSP2']",0111294,604403,,C1858673,,,,C565810,,,,
mondo:0011462,pyogenic arthritis-pyoderma gangrenosum-acne syndrome,"['pyogenic arthritis, pyoderma gangrenosum and acne', 'papa syndrome', 'pyogenic STERILE arthritis, pyoderma gangrenosum, and acne', 'pyogenic arthritis, pyoderma gangrenosum, and severe cystic acne', 'fra', 'papa', 'Papas', 'familial recurrent arthritis']",0080519,604416,69126,C1858361,"['0.1836', '0.2377', '-1.071', '0.1301', '-0.587', '-0.517', '0.43', '0.2406', '0.0303', '0.286', '0.2279', '0.537', '0.0891', '0.514', '0.2983', '0.5024', '0.1713', '0.01151', '0.2979', '-0.9575', '-0.3857', '-0.805', '-0.2029', '-1.031', '0.486', '0.4553', '-0.4473', '0.3882', '0.4126', '-0.2084', '-0.05246', '-0.3308', '0.0523', '0.336', '0.2856', '0.2078', '-0.0867', '-0.457', '-0.0694', '-0.4233', '-0.2578', '-0.0969', '0.11896', '-0.2683', '0.4495', '-0.2854', '-0.2837', '-0.4343', '-0.7295', '-0.11884', '-0.2573', '-0.231', '0.4114', '0.0538', '-0.02397', '0.1273', '0.1494', '0.2556', '-1.032', '-0.0295', '0.05328', '0.1428', '-0.12', '-0.3394', '0.4185', '0.1236', '0.25', '0.5303', '-0.4446', '0.4067', '-0.268', '-0.3623', '-0.3545', '-0.1747', '-0.1814', '0.594', '-0.678', '0.8364', '0.3894', '-0.2166', '-0.9717', '0.1694', '0.1833', '-0.1957', '-0.0161', '-0.0972', '0.71', '0.4595', '0.3896', '0.00574', '0.6636', '0.231', '-0.04172', '0.1715', '0.7114', '0.2947', '0.2615', '-0.51', '0.0605', '-0.81']",C119055,,C536253,,,,
mondo:0011463,"polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive","['polyneuropathy, lethal neonatal, axonal sensorimotor, autosomal recessive']",,604431,538096,C1858353,,,,C565773,,,,
mondo:0011464,spinocerebellar ataxia type 11,"['spinocerebellar ataxia 11', 'spinocerebellar ataxia type 11', 'SCA11']",0050961,604432,98767,C4304886,"['0.0686', '-0.15', '-0.151', '0.11163', '-0.0742', '-0.907', '0.2888', '0.486', '-0.687', '-1.002', '0.01504', '0.1257', '-0.01926', '0.1637', '0.7603', '-0.4045', '-0.1697', '-0.4678', '0.0475', '-0.8047', '-0.224', '-0.3652', '0.02483', '-0.563', '0.11804', '-0.5376', '-0.4668', '0.1152', '0.00534', '-0.744', '0.1621', '0.391', '-0.3528', '-0.2413', '0.4177', '-0.04', '-0.1416', '0.002209', '0.346', '0.4597', '0.455', '0.09644', '-0.2778', '0.582', '0.482', '-0.372', '0.0783', '0.2338', '0.2112', '-0.3513', '-0.1578', '0.1351', '-0.1334', '-0.7197', '0.1205', '-0.7163', '0.3296', '0.4639', '-0.1411', '0.469', '-0.524', '0.312', '0.1638', '-0.1969', '-0.542', '0.4116', '0.246', '0.3997', '-0.6323', '0.4807', '0.6826', '0.2932', '-0.0759', '-0.596', '0.7876', '0.1635', '0.2', '0.05637', '0.132', '0.4229', '-0.1268', '-0.8647', '0.5796', '0.502', '-0.2275', '-0.562', '0.1349', '0.1157', '0.6562', '0.2954', '0.295', '0.4868', '0.09766', '0.004635', '0.793', '1.099', '0.4404', '0.4937', '-0.1017', '-0.1053']",,,C565772,,,,
mondo:0011465,infundibulocystic basal cell carcinoma,"['basal cell carcinoma, infundibulocystic', 'basal cell carcinoma with follicular differentiation', 'skin infundibulocystic basal cell carcinoma']",4279,604451,,C1304297,,C27540,,C537655,,,,
mondo:0011466,"distal myopathy, Welander type","['muscular dystrophy, distal, late-onset, autosomal dominant', 'WDM', 'myopathy, distal, Swedish', 'distal myopathy, Swedish type', 'Welander distal myopathy, Swedish type', 'Welander distal myopathy']",,604454,603,CN205368,"['-0.11273', '-0.322', '-0.3394', '-0.00873', '-0.1722', '-0.638', '0.05316', '1.295', '-0.906', '-0.7188', '-0.1521', '0.4084', '-0.332', '0.515', '0.2896', '0.1333', '-0.2502', '-0.484', '-0.309', '-0.53', '0.2362', '0.0612', '0.3591', '0.509', '-0.091', '-0.3022', '-0.03024', '-0.1414', '-0.628', '-0.02902', '0.521', '-0.2952', '-0.1503', '-0.2131', '0.185', '-0.1329', '-0.2717', '-0.2515', '0.1809', '-0.1412', '-0.5083', '-0.865', '-0.07275', '0.4568', '0.459', '-0.0659', '-0.4006', '0.4766', '0.2969', '0.319', '0.02295', '-0.1433', '-0.32', '-0.8022', '-0.0789', '-0.2773', '1.018', '0.07007', '-0.2605', '-0.202', '0.327', '0.1617', '-0.10223', '-0.0817', '-0.68', '0.2625', '0.05148', '0.147', '-0.3608', '-0.2135', '-0.05994', '-0.3928', '-0.0771', '0.3481', '0.544', '0.04272', '-0.3486', '0.1953', '-0.641', '-0.8423', '0.431', '-0.116', '1.124', '0.7896', '-0.0552', '0.649', '-0.4932', '0.2458', '0.3037', '-0.1589', '0.3972', '-0.2847', '0.09296', '0.3584', '0.659', '-0.1416', '0.708', '-0.4812', '-0.367', '-0.2106']",,,,,,,
mondo:0011468,"hereditary motor and sensory neuropathy, Okinawa type","['hereditary motor and sensory neuropathy, proximal type, formerly', 'hereditary motor and sensory neuropathy, proximal type', 'HMSNO', 'HMSNP', 'neuropathy, hereditary motor and sensory, Okinawa type']",,604484,90117,,"['-0.04932', '0.03058', '0.1332', '-0.357', '-0.09827', '-0.311', '-0.1548', '0.578', '-0.3591', '0.2219', '-0.1786', '0.4177', '-0.4321', '-0.1217', '0.0735', '0.2095', '0.11774', '-0.2443', '0.1354', '-0.731', '0.1587', '-0.432', '-0.05093', '0.899', '0.2454', '0.3474', '0.1724', '-0.466', '-0.2737', '-0.6206', '0.3882', '0.03305', '0.2913', '-0.01894', '-0.01834', '-0.31', '-0.2206', '-0.1802', '0.02467', '-0.4893', '-0.351', '-0.5874', '-0.03876', '0.3347', '-0.1484', '-0.259', '-0.03952', '0.2952', '-0.1625', '0.1453', '0.0873', '0.0703', '-0.271', '-0.4302', '0.1235', '-0.1954', '0.57', '-0.4412', '-0.4224', '0.09625', '0.02682', '-0.03244', '0.34', '-0.04462', '-0.698', '0.0547', '0.1111', '0.649', '-0.1825', '0.1549', '-0.332', '-0.1082', '0.0228', '-0.1638', '0.6426', '0.3171', '-0.05798', '0.2487', '0.1827', '-0.281', '-0.0758', '-0.025', '0.4004', '0.4478', '-0.3613', '0.5537', '-0.2136', '0.1266', '0.3425', '-0.0803', '0.397', '0.172', '0.158', '-0.0739', '0.51', '0.3113', '0.307', '-0.0745', '-0.519', '0.1407']",,,C535717,,,,
mondo:0011469,congenital amegakaryocytic thrombocytopenia,"['CAMT', 'thrombocytopenia, congenital amegakaryocytic', 'congenital amegakaryocytic thrombocytopenic purpura', 'thrombocytopenia congenital amegakaryocytic', 'amegakaryocytic thrombocytopenia, congenital']",0090118,604498,3319,C1327915,"['-0.3691', '-0.05865', '-0.1752', '-0.03537', '0.5835', '0.0476', '-0.1664', '1.2', '-0.4138', '-0.5166', '-0.2064', '0.1366', '-0.406', '-0.1798', '0.07367', '-0.4705', '-0.61', '0.05902', '-0.0271', '-0.8613', '0.234', '0.1348', '0.5967', '-0.989', '0.339', '-0.3232', '0.2808', '0.05365', '-0.1919', '0.0435', '0.0967', '0.06506', '0.3564', '0.395', '-0.115', '0.0987', '-0.3608', '-0.523', '-0.67', '0.2952', '0.1345', '0.2366', '0.49', '-0.4954', '-0.2075', '0.1483', '-0.4453', '0.3936', '-0.05307', '-0.4475', '0.11676', '0.2166', '0.1731', '0.08356', '-0.4358', '0.2168', '-0.01883', '0.1798', '-0.6284', '0.1032', '-0.1978', '0.05328', '0.02734', '-0.6514', '-0.1923', '-0.701', '0.8354', '0.396', '-0.384', '0.5293', '0.1997', '-0.1869', '0.1036', '-0.0822', '0.3984', '-0.02081', '-0.004753', '-0.2683', '-0.2228', '0.267', '-0.25', '-0.001124', '0.419', '-0.00885', '-0.006996', '-0.2227', '0.3936', '0.505', '0.0599', '-0.3115', '0.5825', '0.3494', '0.3992', '-0.4387', '-0.08813', '0.603', '0.5874', '-0.9077', '0.0778', '-0.0486']",C115207,,C535982,,,,
mondo:0011470,"hyperlipidemia, combined, 2","['hyperlipidemia, combined, 2', 'hyperlipidemia, familial combined, 2', 'hyperlipidemia, combined, type 2', 'hyplip2']",,604499,,C1858308,,,,C565766,,,,
mondo:0011471,inflammatory bowel disease 3,"['inflammatory bowel disease 3', 'inflammatory bowel disease type 3', 'IBD3']",0110891,604519,,C1858303,,,,C565764,,,,
mondo:0011472,epidermolysis bullosa simplex due to plakophilin deficiency,"['ectodermal dysplasia skin fragility syndrome', 'ectodermal dysplasia - skin fragility syndrome', 'ectodermal dysplasia/skin fragility syndrome', 'McGrath syndrome', 'Mcgrath syndrome', 'ectodermal dysplasia-skin fragility syndrome']",,604536,158668,C1858302,"['0.7104', '-0.1407', '-0.538', '-0.005615', '0.165', '-0.545', '-0.583', '0.4329', '-0.2024', '-0.67', '0.2598', '-0.2642', '-0.9146', '0.2379', '-0.7207', '0.1692', '0.392', '-1.025', '-0.505', '-0.8877', '-0.182', '-0.1322', '0.4075', '0.308', '0.1488', '0.2715', '-1.074', '0.769', '-0.416', '-0.9214', '0.09265', '-0.10205', '-0.4592', '0.1299', '0.2489', '-0.0646', '-1.014', '0.2434', '0.951', '-0.6226', '0.2756', '-0.641', '0.03476', '0.00118', '0.2329', '-0.08417', '-0.2114', '0.1282', '0.546', '-0.4329', '-0.453', '-0.746', '0.551', '-0.2002', '-0.12006', '-0.5977', '-0.2585', '0.876', '-0.796', '-0.05182', '-0.06586', '0.4807', '0.1022', '0.187', '1.189', '0.705', '0.3953', '0.2391', '-0.5845', '0.4587', '-0.11127', '-0.0651', '-0.3826', '-0.2695', '-0.1173', '0.1569', '0.119', '0.1835', '0.1061', '-0.1659', '-0.834', '-0.07513', '-0.2896', '-0.2786', '0.4521', '0.3896', '-1.132', '0.686', '0.981', '0.337', '-0.2842', '0.2942', '-0.05682', '0.789', '0.0936', '0.8213', '0.1497', '-0.4685', '0.835', '-0.1075']",,,C536183,,,,
mondo:0011473,Leber congenital amaurosis 5,"['Leber congenital amaurosis caused by mutation in LCA5', 'LCA5', 'Leber congenital amaurosis type 5', 'LCA5 Leber congenital amaurosis', 'Leber congenital amaurosis 5', 'amaurosis congenita of Leber, type 5']",0110215,604537,,C1858301,,,,C536602,,H35.5,,
mondo:0011474,progressive familial heart block type IB,"['Pfhbib', 'progressive familial heart block, type IB', 'heart block progressive familial type 1B', 'TRPM4 progressive familial heart block', 'progressive familial heart block type 1B', 'progressive familial heart block, type 1B', 'PFHB1B', 'progressive familial heart block caused by mutation in TRPM4']",0111076,604559,,,,,,C567037,426.6,,,
mondo:0011475,Charcot-Marie-Tooth disease type 4B2,"['Charcot-Marie-Tooth disease, with focally folded myelin sheaths, autosomal recessive, type 4B2', 'Charcot-Marie-Tooth neuropathy type 4B2', 'autosomal recessive Charcot-Marie-Tooth disease with focally folded myelin sheaths type 4B2', 'Charcot-Marie-Tooth disease, type 4B2, with early-onset glaucoma', 'Charcot-Marie-Tooth neuropathy, type 4B2, with early-onset glaucoma', 'Charcot-Marie-Tooth disease type 4 caused by mutation in SBF2', 'Charcot-Marie-Tooth disease, type 4B2', 'CMT4B2', 'Charcot Marie Tooth disease type 4B2', 'SBF2 Charcot-Marie-Tooth disease type 4', 'CMT 4B2', 'Charcot-Marie-Tooth neuropathy, type 4B2']",0110190,604563,99956,C1858278,"['-0.1715', '0.09625', '0.0352', '0.26', '-0.1248', '-0.2174', '-0.3848', '0.7056', '-0.65', '-0.1603', '0.1531', '0.2241', '-0.3784', '0.3474', '-0.2307', '-0.4556', '-0.1635', '-0.299', '-0.5063', '-0.3125', '0.449', '0.2595', '-0.0996', '0.6797', '0.1646', '0.521', '0.10815', '0.3872', '0.2184', '0.11896', '0.1942', '-0.7114', '0.08936', '0.0823', '0.2566', '-0.644', '-0.3098', '-0.2089', '0.4434', '-0.1471', '-1.137', '-0.713', '-0.4197', '0.3022', '-0.428', '-0.1313', '0.0735', '-0.04352', '-0.02623', '0.01111', '0.2019', '-0.013466', '-0.4731', '-1.149', '0.4236', '-0.1627', '0.339', '0.11475', '-0.655', '0.00229', '-0.38', '-0.1129', '0.345', '0.73', '-0.695', '1.067', '0.0463', '0.7637', '-0.5728', '0.422', '-0.754', '0.289', '0.2585', '0.05145', '0.9927', '0.5034', '-0.5234', '0.6875', '0.0349', '-0.321', '0.1498', '-0.276', '0.4185', '0.901', '0.121', '-0.0822', '0.358', '0.7524', '0.7314', '0.502', '0.3489', '-0.2947', '-0.01755', '0.4885', '0.5312', '0.595', '0.388', '-0.4397', '-0.03534', '0.2937']",,,C535421,,,,
mondo:0011476,MHC class I deficiency,"['BLSI', 'immunodeficiency by defective expression of HLA class 1', 'Bls, type 1', 'Bare lymphocyte syndrome, type 1', 'HLA Class 1 deficiency', 'bare lymphocyte syndrome type I', 'BLS, type I', 'immunodeficiency by defective expression of HLA class type 1', 'Bare lymphocyte syndrome type 1', 'BLS type 1', 'bare lymphocyte syndrome, type I, due to TAP2 deficiency', 'BARE lymphocyte syndrome, type I', 'HLA CLASS I deficiency']",0060009,604571,34592,C1858266,"['-0.1732', '-0.005814', '-0.1752', '-0.4744', '-0.0907', '-0.10645', '0.6343', '-0.3044', '0.00434', '0.10065', '0.12366', '-0.0777', '0.08185', '0.1603', '0.00574', '0.1833', '0.333', '-0.07434', '-0.09155', '-0.747', '-0.1528', '-0.1896', '1.126', '0.119', '0.2988', '0.2253', '0.0698', '0.094', '-0.1497', '-0.2854', '0.483', '0.2445', '0.326', '-0.008705', '0.03052', '0.07355', '-0.4182', '-0.11273', '-0.3088', '-0.581', '-0.0835', '-0.1592', '0.01102', '0.03088', '-0.11816', '-0.589', '-0.2274', '-0.4995', '-0.0928', '0.4443', '0.2522', '-0.3342', '0.2031', '0.1782', '-0.509', '-0.5127', '0.03017', '-0.2291', '-0.26', '0.12335', '0.07324', '0.038', '-0.02022', '0.4834', '0.301', '-0.006306', '0.403', '0.2104', '-0.0945', '0.2737', '-0.046', '-0.541', '0.00585', '0.2482', '0.2922', '0.263', '0.5117', '0.3018', '0.399', '0.0751', '-0.4475', '-0.0877', '0.313', '0.3267', '-0.363', '-0.3508', '0.3218', '0.3777', '0.2522', '-0.08875', '0.5586', '0.4685', '-0.2369', '-0.1616', '0.896', '0.71', '0.155', '-0.4895', '0.0618', '0.29']",,,,,,,
mondo:0011477,"tooth agenesis, selective, 3","['tooth agenesis, selective, 3', 'STHAG3', 'PAX9 tooth agenesis', 'tooth agenesis, selective, type 3', 'hypodontia/oligodontia 3', 'tooth agenesis caused by mutation in PAX9']",,604625,,C1970291,,,,C567036,,,,
mondo:0011478,"growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia","['growth and developmental retardation, ocular ptosis, cardiac defect, and anal atresia', 'growth and developintellectual disability, ocular ptosis, cardiac defect, and anal atresia', 'Roca-Weidemann syndrome', 'Roca syndrome']",,604690,,C1858182,,,,C565755,,,,
mondo:0011479,postural orthostatic tachycardia syndrome,"['postural tachycardia syndrome due to NET deficiency', 'familial orthostatic tachycardia due to norepinephrine transporter deficiency', 'POTS', 'orthostatic intolerance due to NET deficiency', 'soldiers heart', 'neurocirculatory asthenia', 'Soldiers heart', 'irritable heart', 'orhtostatic intolerance', 'orthostatic intolerance']",0111154,604715,443236,,"['0.4158', '0.403', '0.1006', '0.4043', '-0.258', '-0.2024', '0.06067', '0.963', '0.1984', '-0.1604', '0.427', '-0.0453', '0.4783', '0.2417', '-0.1279', '-0.1344', '-0.5986', '0.3982', '-0.6343', '-0.2097', '0.5386', '0.51', '0.4426', '0.3127', '-0.2246', '-0.9956', '-0.1716', '0.3264', '-0.03143', '-0.0477', '0.283', '0.599', '0.1442', '-0.3186', '-0.472', '-0.3066', '0.04984', '0.2009', '0.729', '-0.8057', '0.505', '0.2346', '0.56', '-0.05', '0.4111', '-0.1669', '-0.6045', '0.0878', '0.155', '0.1864', '0.002926', '0.44', '-0.10266', '0.0638', '-0.311', '0.03543', '-0.2563', '0.3892', '-0.8257', '-0.983', '-0.4312', '0.7314', '0.5', '-0.8765', '-0.34', '0.6406', '0.467', '0.673', '-0.3618', '0.214', '-0.1682', '0.644', '0.1323', '-0.781', '0.3508', '0.7485', '0.1552', '0.1234', '-0.6895', '0.2286', '0.10974', '-0.2455', '0.2222', '0.10175', '0.2473', '0.1741', '0.381', '-0.2068', '1.14', '0.3804', '0.03842', '-0.394', '-0.07965', '0.1438', '0.7134', '0.3938', '0.003155', '-0.2495', '-1.019', '0.2715']",C85020,1000645,D054972,,,,
mondo:0011480,autosomal dominant nonsyndromic hearing loss 20,"['deafness, autosomal dominant 20', 'autosomal dominant deafness 20', 'deafness, autosomal dominant 20/26', 'deafness, autosomal dominant type 20', 'ACTG1 autosomal dominant nonsyndromic deafness', 'DFNA26', 'autosomal dominant nonsyndromic deafness caused by mutation in ACTG1', 'autosomal dominant nonsyndromic deafness type 20', 'DFNA20', 'autosomal dominant nonsyndromic deafness 20']",0110550,604717,,C1858172,,,,C565754,,,,
mondo:0011481,craniosynostosis 2,"['Warman Mulliken Hayward syndrome', 'craniosynostosis 2', 'craniosynostosis, Warman type', 'Warman-Mulliken-Hayward syndrome', 'CRS2', 'craniosynostosis Warman type', 'MSX2-related craniosynostosis', 'craniosynostosis type 2']",,604757,1541,,"['0.523', '-0.3188', '0.1375', '-0.0959', '0.0335', '-0.1315', '-0.3557', '0.6494', '-0.916', '-0.7295', '-0.2644', '-0.296', '0.2269', '0.3271', '-0.2861', '-0.2129', '0.8154', '-0.7764', '-0.03047', '-1.222', '-0.06573', '0.718', '0.2659', '-0.2445', '0.7153', '0.814', '-0.641', '-0.01021', '0.51', '0.2708', '-0.3025', '0.298', '-0.02425', '-0.3894', '-0.4836', '0.374', '-0.263', '-0.3528', '-0.581', '-0.3198', '0.5327', '0.1393', '-0.05893', '-1.088', '0.6606', '-0.4834', '0.2279', '0.1691', '-0.00391', '-0.4668', '-0.09827', '-0.0344', '0.1039', '-0.5396', '-0.0796', '-0.4165', '-0.606', '-0.1698', '-0.515', '0.352', '-0.4253', '-0.434', '-0.0708', '0.1324', '-0.685', '0.2452', '-0.4365', '0.624', '-0.1161', '1.256', '-0.2825', '1.311', '0.4624', '-0.656', '-0.137', '0.776', '0.1829', '0.010666', '-0.833', '-0.678', '0.1716', '0.1954', '-0.169', '0.521', '0.5513', '0.0736', '-0.1166', '0.2644', '0.335', '0.496', '-0.8003', '0.4026', '0.1248', '0.1643', '0.3333', '-0.000465', '-0.03186', '-0.3398', '0.483', '-0.3074']",,,,,,,
mondo:0011482,dilated cardiomyopathy 1I,"['familial isolated dilated cardiomyopathy caused by mutation in DES', 'dilated cardiomyopathy type 1I', 'cardiomyopathy, dilated, type 1I', 'CMD1I', 'cardiomyopathy, dilated, 1I', 'DES familial isolated dilated cardiomyopathy']",0110431,604765,,C1858154,,,,C565752,,,,
mondo:0011483,polycystic bone disease,"['Pcbd', 'polycystic bone disease']",,604771,,C1858143,,,,C536324,,,,
mondo:0011484,catecholaminergic polymorphic ventricular tachycardia 1,"['CPVT1', 'ARVC2', 'CVPT1', 'arrhythmogenic right ventricular dysplasia type 2', 'ventricular tachycardia, stress-induced polymorphic', 'catecholaminergic polymorphic ventricular tachycardia type 1', 'ventricular tachycardia, catecholaminergic polymorphic, 1', 'familial isolated arrhythmogenic right ventricular dysplasia caused by mutation in RYR2', 'ventricular tachycardia, catecholaminergic polymorphic, 1, with or without atrial dysfunction and/or dilated cardiomyopathy', 'arrhythmogenic right ventricular cardiomyopathy 2', 'RYR2 familial isolated arrhythmogenic right ventricular dysplasia', 'arrhythmogenic right ventricular dysplasia, familial, 2', 'arrhythmogenic right ventricular dysplasia, familial, type 2', 'familial arrhythmogenic right ventricular dysplasia 2', 'ARVD2', 'arrhythmogenic right ventricular dysplasia 2']",0110071,604772,,C4053736,,C123414,,C563409,,I47.2,,
mondo:0011485,autosomal recessive congenital ichthyosis 5,"['autosomal recessive congenital ichthyosis type 5', 'ichthyosis, lamellar, 3', 'ichthyosis, lamellar, 3, formerly', 'ichthyosis, Nonlamellar and Nonerythrodermic, congenital, autosomal recessive', 'type 3 lamellar ichthyosis', 'LI3, formerly', 'ichthyosis lamellar 3', 'ichthyosis, congenital, autosomal recessive type 5', 'ichthyosis congenita III', 'lamellar ichthyosis, type 3', 'NNCI', 'ARCI5', 'ichthyosis congenita 3', 'autosomal recessive congenital nonlamellar and nonerythrodermic ichthyosis', 'ichthyosis, NONLAMELLAR and NONERYTHRODERMIC, congenital, autosomal recessive', 'ichthyosis, congenital, autosomal recessive 5']",0060714,604777,,,,,,C537265,,,,
mondo:0011486,congenital muscular dystrophy 1B,"['MDC1B', 'muscular dystrophy, congenital, 1B', 'congenital muscular dystrophy type 1B', 'CMD1B']",0110634,604801,98893,C1858118,,,,C565748,,,,
mondo:0011487,Huntington disease-like 3,"['Huntington disease-like 3', 'HDL3', 'Huntington disease-like neurodegenerative disorder, autosomal recessive', 'Huntington disease-like type 3']",,604802,157946,C1858114,,,,C565747,,,,
mondo:0011488,"microcephaly 3, primary, autosomal recessive","['CDK5RAP2 autosomal recessive primary microcephaly', 'autosomal recessive primary microcephaly caused by mutation in CDK5RAP2', 'MCPH3', 'microcephaly 3, primary, autosomal recessive']",0070286,604804,,C1858108,,,,C565746,,,,
mondo:0011489,hereditary spastic paraplegia 12,"['spastic paraplegia 12', 'SPG12', 'hereditary spastic paraplegia type 12', 'autosomal dominant spastic paraplegia 12', 'spastic paraplegia 12, autosomal dominant', 'autosomal dominant spastic paraplegia type 12', 'RTN2 hereditary spastic paraplegia', 'hereditary spastic paraplegia caused by mutation in RTN2']",0110765,604805,100993,C1858106,"['-0.2354', '0.2134', '-0.12335', '-0.2264', '-0.1072', '-0.807', '-0.3145', '0.08435', '-0.582', '-0.3618', '0.001606', '-0.03223', '-0.1511', '0.3423', '0.7334', '0.3064', '-0.1876', '-0.216', '0.3652', '-0.3545', '0.287', '-0.1075', '0.1969', '0.2482', '0.0967', '0.0523', '0.0743', '-0.06964', '-0.3591', '-0.2083', '0.2462', '0.3694', '-0.0325', '0.3635', '0.0221', '-0.5225', '-0.501', '-0.3228', '-0.2788', '-0.4094', '0.0412', '-0.774', '-0.02654', '0.306', '-0.1072', '-0.4885', '-0.3757', '0.3743', '-0.05505', '0.0696', '-0.2776', '0.2983', '-0.5254', '-0.54', '-0.1175', '-0.6157', '0.761', '-0.2686', '-0.4797', '0.3418', '-0.09705', '-0.3018', '0.2812', '0.3123', '-0.539', '0.0718', '0.2693', '0.686', '-0.2306', '0.4836', '-0.1339', '-0.2448', '0.3135', '-0.4998', '0.9307', '0.4617', '-0.2651', '0.1562', '-0.1432', '-0.2659', '-0.137', '-0.3738', '0.7563', '1.05', '0.0774', '0.1065', '-0.1052', '0.1965', '0.154', '-0.2126', '0.7515', '-0.003387', '0.0976', '0.458', '0.803', '0.6523', '0.7485', '-0.01909', '-0.2384', '0.1171']",,,C537484,,,,
mondo:0011490,diffuse panbronchiolitis,"['panbronchiolitis, diffuse', 'DPb', 'PBLT']",,604809,171700,C0878555,,,,C536174,491.8,,10062952,
mondo:0011491,"epilepsy, idiopathic generalized, susceptibility to, 7","['EIG7', 'epilepsy, idiopathic generalized, susceptibility to, 7', 'myoclonic epilepsy, juvenile, 2', 'epilepsy, juvenile myoclonic']",0111321,604827,307,,,,,,,,,
mondo:0011492,"mandibulofacial dysostosis syndrome, Bauru type","['mandibulofacial dysostosis syndrome, Bauru type']",,604830,,C1858101,,,,C565744,,,,
mondo:0011493,Stickler syndrome type 2,"['STL2', 'Stickler syndrome, beaded vitreous type', 'Stickler syndrome, type 2', 'COL11A1 Stickler syndrome', 'STL 2', 'Stickler syndrome, vitreous type 2', 'STICKLER syndrome, type II', 'Stickler syndrome type II', 'Stickler syndrome caused by mutation in COL11A1']",0080675,604841,90654,C1858084,"['0.899', '0.0727', '-0.2201', '0.2188', '0.4922', '-0.837', '-0.2566', '0.9985', '-1.173', '-0.5825', '0.5156', '-0.5454', '-0.2356', '0.804', '0.11365', '-0.0873', '-0.3013', '0.651', '-0.659', '0.05408', '-0.1915', '0.1997', '0.3406', '0.2494', '0.11395', '0.2546', '-0.8223', '0.2847', '0.9854', '0.901', '0.1903', '-0.1209', '-0.4038', '0.3735', '-0.384', '-0.0752', '-0.1357', '0.01895', '0.1008', '-0.5103', '0.6987', '0.4438', '-0.4072', '-0.1001', '-0.5205', '-0.541', '-0.02463', '-0.0602', '0.4841', '-0.01346', '-0.311', '0.4688', '0.486', '-0.2615', '0.3032', '-0.3772', '-0.257', '0.3608', '-0.171', '-0.3108', '0.8003', '0.04813', '-0.0226', '0.1536', '-0.4236', '0.1715', '0.4016', '0.3062', '-0.4407', '0.4902', '0.1398', '0.343', '-0.0751', '-0.728', '0.3032', '0.1384', '0.498', '0.56', '0.3662', '0.7354', '-0.2286', '-0.1622', '0.08', '0.7407', '-0.662', '-0.087', '0.3591', '0.728', '0.1685', '0.183', '-0.5996', '0.6626', '0.3096', '0.3098', '0.4644', '0.2996', '0.6055', '-0.4927', '-0.3914', '0.3015']",C74985,,C537493,,,,
mondo:0011494,"hyaluronan metabolism, defect 1N","['hyaluronan metabolism, defect IN', 'hyaluronan metabolism, defect type 1N']",,604855,,C1858083,,,,C565742,,,,
mondo:0011496,mild spondyloepiphyseal dysplasia due to COL2A1 mutation with early-onset osteoarthritis,"['Namaqualand hip dysplasia', 'OSCDP', 'osteoarthritis with mild chondrodysplasia']",,604864,93279,C1858079,"['-0.1687', '0.3745', '0.1665', '-0.0353', '0.4612', '-0.782', '-0.1848', '0.528', '-0.444', '-0.4424', '0.2563', '0.7866', '0.07025', '0.571', '0.1146', '-0.000494', '0.3462', '-0.004353', '-0.542', '-0.4634', '0.6016', '0.3457', '0.1887', '-0.3655', '-0.536', '0.3435', '0.2534', '-0.4683', '0.2805', '-0.201', '0.0867', '-0.2327', '0.492', '0.336', '0.6436', '-0.2167', '-0.05353', '-0.6', '0.3818', '-0.783', '0.7466', '0.1746', '-0.883', '0.6714', '-0.2517', '0.01039', '0.2324', '0.06537', '0.691', '-0.3152', '0.3945', '0.01415', '0.929', '0.2715', '0.543', '-0.2795', '-0.03918', '-0.0886', '0.005486', '-0.2603', '0.6587', '-0.0782', '-0.7163', '-0.579', '-0.699', '-0.00747', '0.4', '0.89', '0.159', '0.582', '-0.04962', '0.1146', '0.03345', '-0.614', '0.293', '0.3442', '-0.2123', '1.669', '0.1442', '-0.4055', '-0.482', '-0.1934', '0.06052', '0.1108', '0.649', '0.3052', '-0.197', '0.6196', '0.7925', '-0.0532', '-0.12286', '0.7407', '-0.2333', '-0.03674', '-0.1582', '0.2786', '0.1545', '-0.3757', '0.01332', '-0.2856']",,,C565740,755.63,,,
mondo:0011497,hereditary North American Indian childhood cirrhosis,"['NAIC', 'NORTH American Indian childhood cirrhosis']",,604901,168583,C1858051,,,,C565737,,,,
mondo:0011498,schizophrenia 9,"['schizophrenia 9', 'schizophrenia 9, susceptibility to', 'SCZD9', 'schizophrenia susceptibility locus, chromosome 1Q42-related', 'schizophrenia 9 with or without an affective disorder', 'schizophrenia type 9']",0070085,604906,,C1858050,,,,,,,,
mondo:0011499,Okamoto syndrome,"['congenital hydronephrosis with cleft palate, characteristic facies, hypotonia, and mental retardation', 'hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and intellectual disability', 'hydronephrosis, congenital, with cleft palate, characteristic facies, hypotonia, and mental retardation', 'Okamoto syndrome', 'congenital hydronephrosis with cleft palate, characteristic facies, hypotonia, and intellectual disability']",,604916,2729,C1858043,,,,C565736,,,,
mondo:0011500,Becker nevus syndrome,"['hairy epidermal nevus syndrome', 'Becker nevus syndrome', 'pigmentary hairy epidermal nevus']",,604919,64755,C1858042,,,,C565735,,,,
mondo:0011501,wormian bone-multiple fractures-dentinogenesis imperfecta-skeletal dysplasia,"['cortical defects, WORMIAN bones, and dentinogenesis imperfecta', 'cortical defects wormian bones and dentinogenesis imperfecta', 'Suarez-Stickler syndrome']",,604922,166277,C1858032,,,,C565734,,,,
mondo:0011502,Wolfram syndrome 2,"['WFS2', 'WOLFRAM syndrome 2', 'CISD2 Wolfram syndrome', 'Wolfram syndrome 2', 'Wolfram syndrome type 2', 'Wolfram syndrome caused by mutation in CISD2']",0110630,604928,,C1858028,,,,C565733,,,,
mondo:0011503,cortisone reductase deficiency 1,"['apparent cortisone reductase deficiency', 'hexose-6-phosphate dehydrogenase deficiency', 'cortisone reductase deficiency caused by mutation in H6PD', 'H6PD cortisone reductase deficiency', 'CORTRD1', 'cortisone reductase deficiency 1', 'cortisone reductase deficiency type 1']",0090141,604931,,C3551716,,C131849,,,,,,
mondo:0011504,NDE1-related microhydranencephaly,"['microhydranencephaly', 'MHAC', 'hydranencephaly and microcephaly']",,605013,443162,C1857977,,,,C537555,,,,
mondo:0011505,familial hypobetalipoproteinemia 2,"['hypobetalipoproteinemia, familial, type 2', 'hypobetalipoproteinemia, familial, 2', 'ANGPTL3 hypobetalipoproteinemia', 'FHBL2', 'combined familial hypolipidemia', 'hypobetalipoproteinemia caused by mutation in ANGPTL3', 'hypolipidemia, familial, combined', 'familial hypobetalipoproteinemia type 2']",0111061,605019,,C1857970,,,,C565732,,,,
mondo:0011506,familial infantile myoclonic epilepsy,"['myoclonic epilepsy, infantile, familial', 'myoclonic epilepsy, familial infantile', 'FIME', 'Eim', 'familial infantile myoclonus epilepsy']",,605021,352582,C0917800,"['0.944', '0.2042', '-0.4001', '-0.1478', '-0.57', '-0.5044', '0.887', '0.3865', '-0.656', '-0.503', '0.11865', '-0.2096', '-0.5474', '0.3508', '-0.1572', '0.1353', '-0.3403', '-0.672', '-0.3628', '-0.641', '-0.25', '0.6475', '0.10657', '-0.546', '-0.338', '-0.08215', '-0.1799', '-0.1473', '-0.447', '0.29', '0.2896', '-0.7227', '0.2622', '0.3174', '0.8423', '0.4614', '-0.04645', '0.0488', '-0.04373', '-0.2383', '-0.098', '-0.511', '0.08453', '-0.3052', '-0.4802', '-0.836', '-0.281', '0.3186', '0.4443', '0.524', '-0.235', '0.1123', '0.08496', '-0.549', '0.0195', '-0.3853', '-0.1129', '0.12335', '-0.04242', '0.2437', '-0.7236', '0.602', '0.722', '-0.1539', '-0.5034', '1.448', '0.2036', '-0.06088', '-0.969', '0.7256', '1.037', '0.9927', '0.005745', '-0.4377', '0.1552', '0.69', '1.154', '0.3887', '-0.3684', '0.5103', '-0.0704', '0.863', '0.4753', '0.1121', '0.4443', '0.1333', '0.286', '0.6724', '0.812', '0.4631', '0.0948', '0.0709', '-0.2544', '0.00364', '0.2007', '0.3254', '0.379', '-0.5493', '0.266', '0.3076']",,,,,,,
mondo:0011507,"diabetes mellitus, congenital autoimmune","['diabetes mellitus, congenital autoimmune']",,605026,,C1857958,,,,C565730,,,,
mondo:0011508,"lymphoma, non-Hodgkin, familial","['lymphoma, non-Hodgkin', 'lymphoma, non-Hodgkin, somatic', 'lymphoma, non-Hodgkin, familial', 'non-Hodgkin lymphoma', 'lymphoma, follicular, somatic']",,605027,,,,,,,202.80,,,
mondo:0011509,"low density lipoprotein cholesterol, mild elevation of","['Ldlc, mild elevation of', 'low density lipoprotein cholesterol, mild elevation of']",,605028,,,,,,,,,,
mondo:0011510,Bohring-Opitz syndrome,"['BOPS', 'Opitz trigonocephaly-like syndrome', 'Bohring syndrome', 'Bos syndrome', 'Bohring-Opitz syndrome', 'C-like syndrome', 'BOHRING-Opitz syndrome', 'Oberklaid-Danks syndrome']",,605039,97297,C0796232,"['0.1173', '0.1887', '0.2742', '-0.3528', '0.121', '-0.636', '0.08185', '0.6772', '-0.7104', '-0.663', '-0.1971', '-0.03278', '0.2177', '-0.2866', '-0.558', '0.2646', '0.9277', '-0.08636', '-0.05402', '-0.376', '0.2993', '-0.07605', '-0.3967', '-0.1271', '0.2708', '0.04492', '-0.2214', '0.1478', '0.2834', '-0.3794', '0.162', '-0.09467', '0.358', '-0.02362', '0.0567', '0.101', '-0.1014', '-0.1904', '-0.1854', '-0.3718', '-0.0956', '-0.2776', '-0.02228', '-0.397', '-0.1067', '-0.1895', '0.2908', '0.295', '-0.1504', '0.4553', '-0.5293', '0.3608', '-0.1317', '0.2378', '-0.3594', '-0.449', '0.4373', '-0.03586', '-0.04425', '0.2086', '0.0769', '0.06647', '-0.79', '-0.2421', '0.3293', '-0.3264', '-0.105', '0.3823', '-0.2783', '0.4888', '-0.257', '0.642', '0.05264', '0.12134', '-0.3835', '0.5933', '0.3135', '-0.1104', '-0.3716', '-0.01224', '-0.1383', '0.3037', '0.0957', '0.371', '0.1473', '0.597', '-0.2236', '0.1654', '-0.007473', '0.4724', '-0.05746', '0.342', '-0.00552', '-0.4854', '0.524', '0.2644', '0.757', '-0.3657', '0.3718', '-0.0908']",C131533,,C537419,,,,
mondo:0011511,"clavicular hypoplasia, zygomatic arch hypoplasia, and micrognathia","['clavicular hypoplasia, zygomatic arch hypoplasia, and micrognathia', 'Chzam']",,605040,,C1857942,,,,C565729,,,,
mondo:0011512,Brooke-Spiegler syndrome,"['Spiegler-Brooke syndrome', 'Brooke-Spiegler syndrome', 'Bss', 'BRSS', 'CYLD cutaneous syndrome']",0050693,605041,79493,C1857941,"['0.2468', '-0.2188', '-0.2148', '-0.332', '-0.492', '0.08514', '0.091', '0.07294', '-0.00837', '-0.4072', '0.013016', '0.3542', '0.10846', '0.0979', '-0.2314', '0.3088', '0.1794', '-0.1632', '0.172', '-0.633', '-0.2172', '-0.01822', '0.2627', '-0.506', '0.05035', '-0.1729', '-0.243', '-0.4624', '0.3743', '-0.2717', '0.7', '-0.1214', '0.2693', '-0.4119', '-0.11475', '0.2708', '-0.4006', '-0.3257', '0.0517', '-0.3645', '0.2688', '-0.10846', '0.4866', '-0.00443', '0.6367', '-0.797', '-0.7847', '-0.265', '-0.3088', '0.04932', '0.1866', '-0.044', '-0.03766', '0.5386', '-0.705', '0.2817', '0.4114', '0.6514', '-0.294', '-0.1967', '0.3196', '0.1038', '-0.4324', '-0.1451', '0.02267', '0.07916', '0.811', '0.7417', '0.3918', '1.272', '-0.1943', '0.1206', '0.3315', '0.295', '-0.1484', '-0.54', '-0.5938', '-0.1864', '-0.2249', '-0.7344', '-0.4019', '0.5684', '0.01243', '-0.01209', '-0.8926', '-0.398', '0.1691', '-0.0657', '0.01915', '0.08954', '0.2334', '0.2913', '-0.4358', '0.4763', '0.9272', '-0.1766', '0.5728', '-0.6177', '0.572', '-0.2332']",,,,239.2,,,
mondo:0011513,"Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology","['Alzheimer disease, familial early-onset, with coexisting amyloid and prion pathology']",,605055,,C1857933,,,,C565728,,,,
mondo:0011514,tricuspid atresia,"['tricuspid atresia (disease)', 'congenital agenesis of the tricuspid valve', 'tricuspid valve atresia', 'tricuspid atresia', 'congenital atresia of tricuspid valve']",0080169,605067,1209,C0243002,,C85202,,D018785,,Q22.4,10049767,0011662
mondo:0011516,early response to neural induction gene,"['early response to neural induction gene', 'Erni']",,605105,,,,,,,,,,
mondo:0011517,pseudohyperaldosteronism type 2,"['hypertension, early-onset, autosomal dominant, with exacerbation in pregnancy', 'early-onset hypertension with exacerbation in pregnancy', 'hypertension, early-onset, autosomal dominant, with Severe exacerbation in pregnancy', 'hypertension due to gain-of-function mutations in the mineralocorticoid receptor', 'hypertension, early-onset, autosomal dominant, with severe exacerbation in pregnancy']",,605115,88660,C1854631,"['-0.1809', '0.138', '-0.3025', '0.00652', '0.0444', '-0.2717', '-0.1008', '0.46', '-0.5854', '-0.3435', '-0.5757', '0.284', '0.6562', '0.2483', '-0.1731', '-0.39', '0.1454', '0.1216', '0.498', '-0.758', '-0.0723', '-0.1238', '0.333', '0.02501', '0.07495', '0.1188', '0.633', '0.2013', '0.1353', '-0.2128', '0.4536', '0.0669', '0.8325', '0.2637', '-0.513', '0.007362', '-0.3274', '0.2524', '-0.0766', '-0.2336', '0.04013', '-0.1278', '0.745', '-0.3652', '-0.2173', '-0.4307', '-0.1608', '0.284', '0.1787', '0.11993', '0.2372', '-0.138', '0.1322', '-0.3809', '0.364', '0.4138', '0.03072', '-0.911', '-0.2389', '0.2607', '0.1407', '0.3843', '0.5176', '-0.5728', '-0.161', '-0.06305', '0.3618', '0.382', '-0.3882', '0.2878', '0.2622', '0.0605', '0.384', '-0.004883', '0.5083', '0.2013', '0.1562', '-0.0662', '-0.03784', '-0.1059', '-0.1411', '0.6777', '0.0928', '-0.2148', '0.1792', '0.349', '0.1357', '0.048', '0.662', '0.1516', '0.4146', '0.22', '-0.0805', '-0.1509', '0.0148', '-0.01872', '0.4397', '-0.7944', '-0.5674', '0.09015']",,,C565359,,,,
mondo:0011518,Wiedemann-Steiner syndrome,"['Wiedemann-Steiner syndrome', 'hairy elbows, short stature, Facial Dysmorphism, and developmental delay', 'Wiedemann Grosse Dibbern syndrome', 'hypertrichosis-short stature-facial dysmorphism-developmental delay syndrome', 'A syndrome of abnormal facies, short stature, and psychomotor retardation', 'WDSTS']",,605130,319182,,"['-0.376', '0.1927', '0.5522', '-0.406', '0.4724', '-0.639', '0.1245', '0.4236', '-0.5044', '-0.0332', '0.02068', '-0.2252', '0.571', '-0.1602', '0.01056', '0.3103', '0.1298', '-0.4597', '-0.1711', '-0.5703', '-0.1268', '0.1008', '0.1575', '-0.06097', '0.1292', '-0.481', '-0.1958', '0.05563', '0.3064', '0.01167', '0.2903', '-0.07855', '0.1675', '0.1711', '0.1359', '-0.4763', '0.02739', '0.0128', '0.1544', '-0.413', '0.1777', '-0.2678', '-0.03116', '-0.2512', '0.354', '-0.6465', '-0.2148', '0.48', '0.3616', '-0.3147', '-0.6753', '0.146', '-0.135', '0.1353', '-0.10486', '-0.4558', '-0.1614', '0.4197', '-0.1617', '0.1653', '-0.02121', '0.5083', '-0.03894', '0.2478', '0.0655', '0.597', '-0.2172', '0.6675', '-0.1936', '0.1824', '-0.584', '-0.231', '0.06134', '0.5996', '-0.3276', '0.1511', '0.564', '-0.6216', '-0.6807', '0.2646', '0.568', '0.4346', '-0.173', '0.2505', '0.1653', '0.2605', '0.04703', '0.4014', '0.4902', '0.855', '-0.4946', '0.2854', '0.07794', '-0.2041', '0.531', '0.01053', '0.4412', '-0.3918', '0.422', '-0.10016']",,,C536704,,,,
mondo:0011519,autosomal dominant nonsyndromic hearing loss 23,"['autosomal dominant nonsyndromic deafness caused by mutation in SIX1', 'autosomal dominant nonsyndromic deafness type 23', 'deafness, autosomal dominant nonsyndromic sensorineural 23', 'deafness, autosomal dominant 23', 'DFNA 23', 'autosomal dominant deafness 23', 'deafness, autosomal dominant type 23', 'DFNA23', 'autosomal dominant nonsyndromic deafness 23', 'SIX1 autosomal dominant nonsyndromic deafness']",0110553,605192,,C1854594,,,,C565357,,,,
mondo:0011520,"systemic lupus erythematosus, susceptibility to, 2","['systemic lupus erythematosus, susceptibility to, type 2', 'susceptibility to systemic lupus erythematosus 2', 'SLEB2', 'systemic lupus erythematosus, susceptibility to, 2']",,605218,,C1854577,,,,,,,,
mondo:0011521,inflammatory bowel disease 7,"['IBD7', 'inflammatory bowel disease type 7', 'inflammatory bowel disease 7']",0110882,605225,,C1854573,,,,C565353,,,,
mondo:0011522,hereditary spastic paraplegia 14,"['SPG14', 'autosomal recessive spastic paraplegia type 14', 'autosomal recessive spastic paraplegia 14', 'spastic paraplegia 14', 'spastic paraplegia 14, autosomal recessive', 'hereditary spastic paraplegia type 14']",0110767,605229,100995,C1854568,,,,C537486,,,,
mondo:0011523,Bardet-Biedl syndrome 6,"['Bardet-Biedl syndrome 6', 'Bardet-Biedl syndrome type 6', 'BBS6']",0110128,605231,,C1858054,,,,C565738,,,,
mondo:0011524,Dianzani autoimmune lymphoproliferative disease,"['autoimmune lymphoproliferative syndrome without FAS mutations', 'DALD', 'Dianzani form of autoimmune lymphoproliferative disease', 'Dianzani autoimmune lymphoproliferative syndrome', 'Dianzani autoimmune lymphoproliferative disease']",,605233,275523,C2931071,,,,C535950,,,,
mondo:0011525,Carney complex type 2,"['Carney complex, type II', 'CNC2', 'Carney Myxoma-endocrine Complex, type 2', 'Carney complex, type 2']",,605244,,,,,,,,,,
mondo:0011527,Charcot-Marie-Tooth disease type 4E,"['neuropathy, congenital hypomyelinating or AMYELINATING, autosomal recessive', 'Charcot-Marie-Tooth neuropathy type 4E', 'neuropathy, congenital hypomyelinating, 1', 'autosomal recessive congenital hypomyelinating neuropathy', 'congenital hypomyelination neuropathy', 'CHN1', 'neuropathy, congenital hypomyelinating, autosomal dominant', 'neuropathy, congenital hypomyelinating', 'congenital hypomyelinating neuropathy (CHN)', 'NEUROPATHY, CONGENITAL HYPOMYELINATING, 1, AUTOSOMAL RECESSIVE', 'CHN', 'hypomyelinating neuropathy, congenital, 1', 'Charcot-Marie-Tooth disease, type 4E', 'Charcot Marie Tooth disease type 4E', 'Charcot-Marie-Tooth neuropathy, type 4E', 'Charcot-Marie-Tooth disease type 4E', 'hypomyelination, Severe congenital', 'CMT4E', 'autosomal recessive congenital hypomyelinating or amyelinating neuropathy', 'CMT 4E']",0110195,605253,99951,,"['0.0411', '0.0334', '0.168', '0.0305', '0.1425', '-0.2056', '0.04407', '0.6294', '-0.793', '0.002975', '0.234', '0.3289', '-0.633', '0.6123', '-0.526', '-0.1473', '-0.00902', '-0.4614', '-0.5757', '-0.7783', '0.3303', '0.3098', '0.1976', '0.4062', '0.3843', '0.4204', '0.05908', '0.2805', '0.1805', '-0.1882', '0.0352', '-0.5347', '0.1436', '-0.1178', '0.2888', '-1.006', '-0.1123', '0.091', '0.3943', '-0.014854', '-1.415', '-0.4617', '-0.7407', '0.4604', '-0.1877', '-0.2805', '0.2109', '0.06616', '-0.4304', '-0.06247', '-0.1212', '0.2164', '-0.6753', '-1.263', '0.11584', '-0.267', '-0.1023', '0.1627', '-0.665', '-0.229', '-0.5103', '0.2803', '0.71', '0.5835', '-0.685', '1.069', '0.09937', '0.526', '-0.5537', '0.4124', '-0.7026', '0.0522', '0.4106', '-0.1962', '1.064', '0.2732', '-0.311', '0.4888', '0.0908', '-0.678', '0.1478', '-0.0998', '0.514', '0.558', '-0.0748', '-0.355', '0.2468', '0.867', '1.0205', '0.505', '0.1869', '-0.10425', '0.0154', '0.687', '0.4126', '0.7', '0.4412', '-0.3435', '0.0867', '0.3372']",,,C535301,,,,
mondo:0011528,hyper-IgM syndrome type 2,"['HIGM2', 'aid deficiency', 'immunodeficiency with hyper-IgM type 2', 'immunodeficiency with hyper IgM type 2', 'immunodeficiency with hyper-IgM, type 2', 'hyper IgM syndrome 2', 'hyper-IgM syndrome 2', 'AICDA hyper-IgM syndrome', 'hyper-IgM syndrome type 2', 'Activation-induced cytidine deaminase deficiency', 'activation-induced cytidine deaminase deficiency', 'hyper-IgM syndrome caused by mutation in AICDA']",0060758,605258,101089,,"['-0.3984', '0.2803', '0.0996', '-0.04114', '0.1978', '-0.1328', '-0.03598', '-0.1515', '-0.1246', '-0.04807', '-0.096', '0.2054', '0.0502', '-0.0694', '0.01096', '-0.1726', '0.00683', '-0.06995', '-0.08026', '-0.2646', '0.08984', '-0.19', '0.5615', '-0.0744', '0.2607', '0.01493', '0.0765', '0.1608', '0.0892', '-0.2788', '0.1967', '0.4045', '0.3496', '-0.04288', '0.0714', '-0.2161', '-0.07416', '0.0859', '-0.03174', '-0.374', '0.0544', '-0.2474', '0.1318', '-0.1367', '-0.209', '-0.3174', '-0.0799', '-0.06226', '0.2803', '0.0253', '0.1575', '-0.4045', '0.05536', '0.07135', '-0.333', '-0.01828', '0.367', '-0.2676', '-0.3254', '0.19', '-0.001966', '0.1871', '0.0837', '0.03647', '0.294', '-0.09827', '0.2993', '0.03513', '-0.2355', '0.12164', '-0.312', '-0.06964', '-0.04144', '-0.001769', '0.1357', '-0.0538', '-0.00916', '0.1595', '-0.0917', '-0.0985', '-0.1091', '-0.07666', '-0.0906', '0.1117', '-0.3584', '-0.2368', '0.3333', '0.2961', '0.1659', '-0.04648', '0.09717', '0.2437', '-0.06058', '-0.2355', '0.546', '0.0772', '0.2356', '-0.596', '-0.05536', '0.1417']",C129074,,,,,,
mondo:0011529,spinocerebellar ataxia type 13,"['spinocerebellar ataxia 13', 'spinocerebellar ataxia type 13', 'autosomal dominant cerebellar ataxia with mental retardation', 'SCA13', 'autosomal dominant cerebellar ataxia with intellectual disability', 'cerebellar ataxia, autosomal dominant with mental retardation', 'cerebellar ataxia, autosomal dominant with intellectual disability']",0050963,605259,98768,C4304884,"['-0.168', '-0.2642', '-0.1559', '-0.003662', '-0.2408', '-0.776', '0.2783', '0.11475', '-0.6357', '-0.839', '0.06226', '0.2463', '-0.1362', '0.1312', '0.636', '-0.4612', '-0.0864', '-0.2852', '0.1071', '-1.054', '-0.1638', '-0.2646', '0.2937', '-0.6343', '0.3657', '-0.3635', '-0.4739', '0.2299', '-0.1597', '-0.9097', '0.02438', '0.344', '-0.476', '-0.2462', '0.2113', '0.116', '-0.0991', '0.1647', '0.4126', '0.592', '0.304', '0.016', '-0.4468', '0.3857', '0.509', '-0.6655', '0.09314', '0.4707', '0.3655', '-0.02583', '-0.1071', '0.03336', '-0.0833', '-0.4255', '-0.1111', '-0.721', '0.287', '0.5913', '-0.278', '0.4958', '-0.616', '0.263', '0.3374', '-0.1807', '-0.5273', '0.469', '0.289', '0.4739', '-0.4685', '0.4653', '0.7935', '0.3892', '-0.1133', '-0.795', '0.586', '0.4365', '0.204', '0.243', '0.12067', '0.729', '-0.2913', '-0.878', '0.5', '0.637', '-0.3252', '-0.604', '0.3843', '-0.07196', '0.7607', '0.4778', '0.4558', '0.6', '0.01394', '-0.06097', '0.9766', '0.894', '0.5986', '0.5376', '-0.1399', '-0.02351']",,,C537195,,,,
mondo:0011530,"mesomelic dysplasia, Savarirayan type","['mesomelic dysplasia, Savarirayan type', 'triangular tibia and fibular aplasia', 'mesomelic dysplasia Savarirayan type', 'triangular tibia-fibular aplasia syndrome', 'mesomelic dysplasia with absent fibulas and triangular tibias']",,605274,85170,C1854470,,,,C565349,,,,
mondo:0011531,Noonan syndrome 2,"['Noonan syndrome 2', 'Noonan syndrome, autosomal recessive', 'Noonan syndrome type 2', 'NS2', 'Noonan syndrome autosomal recessive', 'autosomal recessive Noonan syndrome']",0060580,605275,,C1854469,,C176930,,C548081,,,,
mondo:0011532,hereditary spastic paraplegia 13,"['spastic paraplegia 13, autosomal dominant', 'autosomal dominant spastic paraplegia type 13', 'hereditary spastic paraplegia type 13', 'spastic paraplegia 13', 'SPG13', 'hereditary spastic paraplegia caused by mutation in HSPD1', 'HSPD1 hereditary spastic paraplegia', 'autosomal dominant spastic paraplegia 13']",0110766,605280,100994,C1854467,"['-0.1986', '0.331', '-0.02197', '-0.3098', '-0.1265', '-0.5923', '-0.4648', '0.2454', '-0.573', '-0.1694', '0.1646', '0.1086', '0.012085', '-0.07135', '0.5093', '-0.11597', '0.10406', '-0.0957', '0.03476', '-0.3528', '0.04364', '-0.1188', '0.03006', '0.1201', '0.0822', '0.1907', '0.05905', '0.0808', '-0.1034', '-0.1284', '-0.00833', '-0.03053', '-0.010605', '0.0132', '-0.05756', '-0.2957', '-0.02893', '-0.02724', '0.0389', '-0.1552', '0.039', '-0.282', '-0.2166', '0.2712', '-0.1721', '-0.2764', '-0.01295', '0.2065', '0.222', '-0.1611', '-0.09985', '0.07947', '-0.357', '-0.1481', '-0.01484', '-0.425', '0.3623', '-0.08264', '-0.3386', '0.1981', '-0.1624', '0.10455', '0.4846', '0.24', '-0.247', '0.3599', '0.3252', '0.4182', '-0.56', '0.2922', '-0.2883', '0.2737', '0.1418', '-0.391', '0.479', '0.256', '-0.03564', '0.2886', '0.11505', '-0.11584', '-0.0874', '-0.1714', '0.588', '0.3896', '-0.2559', '-0.0264', '-0.04254', '0.273', '0.1917', '0.0464', '0.0691', '-0.0637', '0.11383', '-0.02708', '0.747', '0.3962', '0.524', '-0.2078', '-0.1213', '0.2491']",,,C537485,,,,
mondo:0011533,temtamy preaxial brachydactyly syndrome,"['temtamy preaxial brachydactyly syndrome', 'TPBS', 'mental retardation syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies', 'preaxial brachydactyly syndrome, Temtamy type', 'preaxial brachydactyly syndrome, TEMTAMY type', 'TEMTAMY preaxial brachydactyly syndrome', 'intellectual disability syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies']",0050814,605282,363417,C1854466,"['-0.4731', '-0.02437', '0.776', '-0.2795', '0.6387', '-0.5635', '-0.1431', '0.7515', '-0.685', '-0.0768', '-0.2576', '-0.264', '0.04382', '-0.337', '-0.01634', '0.1655', '0.434', '-0.527', '-0.2854', '-0.4954', '0.3474', '-0.2224', '-0.0628', '-0.0857', '0.5796', '-0.02934', '-0.4814', '-0.2101', '0.4932', '-0.2563', '0.3481', '0.3193', '0.01511', '-0.02231', '0.536', '-0.4236', '-0.1866', '-0.1661', '-0.1309', '-0.613', '-0.0373', '-0.09106', '0.0061', '-0.1637', '0.01743', '-0.611', '-0.0711', '0.4597', '0.2446', '0.1626', '-0.546', '0.1718', '-0.1444', '0.51', '-0.3154', '-0.794', '-0.1835', '-0.2145', '-0.5415', '0.278', '-0.006138', '-0.04202', '0.06903', '0.1252', '-0.1938', '0.2769', '-0.1396', '0.2656', '-0.2058', '0.2429', '-0.6533', '0.2388', '0.4573', '-0.06128', '0.1797', '-0.316', '0.1794', '-0.1009', '-0.5273', '-0.2155', '0.419', '-0.2122', '-0.0985', '0.6577', '-0.1145', '-0.3784', '0.024', '0.9263', '0.2146', '0.6284', '-0.2861', '0.8447', '0.337', '0.00577', '0.4893', '-0.003706', '0.564', '-0.781', '0.9077', '0.305']",,,C536958,,,,
mondo:0011534,Charcot-Marie-Tooth disease type 4G,"['Charcot-Marie-Tooth disease type 4 caused by mutation in HK1', 'Charcot-Marie-Tooth disease, type 4G', 'Charcot-Marie-Tooth neuropathy, type 4G', 'CMT4G', 'neuropathy, hereditary motor and sensory, Russe type', 'Charcot-Marie-Tooth disease, autosomal recessive, type 4G', 'HK1 Charcot-Marie-Tooth disease type 4', 'autosomal recessive Charcot-Marie-Tooth disease type 4G', 'hereditary motor and sensory neuropathy, Russe type', 'HMSNR', 'Charcot-Marie-Tooth neuropathy type 4G', 'hereditary motor and sensory neuropathy Russe type']",0110196,605285,99953,C1854449,"['0.0752', '0.179', '0.2607', '0.1371', '0.1418', '-0.1982', '0.10266', '0.4875', '-0.873', '-0.07166', '0.0136', '0.335', '-0.592', '0.4172', '-0.1588', '-0.1004', '-0.1711', '-0.3928', '-0.6846', '-0.7695', '0.2769', '0.334', '0.2598', '0.592', '0.267', '0.1295', '0.04712', '0.2544', '-0.2314', '-0.1809', '0.1592', '-0.7817', '0.0502', '0.306', '0.5405', '-0.7246', '-0.4897', '-0.12384', '0.4924', '0.04456', '-1.1455', '-0.2996', '-0.4534', '0.398', '-0.4346', '-0.4197', '0.1779', '-0.02', '-0.1368', '0.03522', '0.10724', '0.3108', '-0.536', '-0.918', '0.2368', '-0.1753', '-0.346', '0.4468', '-0.657', '-0.09924', '-0.4268', '-0.0744', '0.6675', '0.903', '-0.612', '1.216', '0.05722', '0.791', '-0.5728', '0.2507', '-0.5825', '-0.01778', '0.3596', '-0.2603', '1.2705', '0.4312', '-0.3936', '0.4607', '-0.1242', '-0.642', '-0.206', '-0.2241', '0.644', '0.6973', '-0.0652', '-0.1599', '0.06305', '0.407', '0.703', '0.2734', '0.1775', '0.03604', '0.0695', '0.3938', '0.341', '0.7446', '0.5977', '-0.725', '-0.138', '0.6567']",,,C535813,,,,
mondo:0011535,split hand-foot malformation 4,"['SHFM4', 'split hand-foot malformation type 4', 'split hand-foot malformation caused by mutation in TP63', 'split-hand/foot malformation type 4', 'TP63 split hand-foot malformation', 'split-hand/foot malformation 4']",0090023,605289,,,,,,C565344,,,,
mondo:0011536,optic atrophy 4,"['optic atrophy 4', 'OPA4']",0111440,605293,,C1854430,,,,C565343,,,,
mondo:0011537,macrocephaly-autism syndrome,"['macrocephaly-intellectual disability-autism syndrome', 'macrocephaly/autism syndrome']",0060867,605309,210548,C1854416,"['-0.2512', '0.2507', '0.3123', '-0.3767', '0.2185', '-0.417', '-0.03326', '0.428', '-0.6343', '-0.08905', '0.07196', '-0.2175', '0.4333', '-0.3572', '0.1301', '0.1825', '0.1862', '-0.1532', '-0.2064', '-0.4143', '0.1521', '-0.03854', '0.2654', '-0.1038', '0.299', '-0.2206', '-0.2186', '0.00634', '0.2488', '-0.2397', '0.4255', '0.10956', '0.4058', '0.1578', '0.2406', '-0.1638', '-0.2097', '-0.2053', '-0.06125', '-0.7026', '0.349', '-0.351', '-0.05338', '-0.1913', '-0.0572', '-0.4512', '0.1644', '0.3928', '0.02705', '-0.1017', '-0.3105', '0.2085', '-0.2207', '0.4172', '0.03543', '-0.596', '-0.1716', '0.1945', '-0.0391', '0.3862', '0.09467', '0.01997', '-0.03128', '0.1362', '0.11127', '0.0638', '0.02948', '0.2455', '-0.3752', '0.4612', '-0.317', '0.12164', '0.1687', '-0.0568', '-0.2805', '0.1803', '0.3281', '-0.1335', '-0.2148', '-0.07086', '0.2766', '0.00738', '-0.2379', '0.5396', '-0.04645', '0.2216', '-0.0732', '0.4941', '0.2086', '0.3958', '-0.1635', '0.2195', '-0.02502', '-0.0734', '0.4795', '-0.002897', '0.396', '-0.2113', '0.4277', '0.314']",,,C565342,,,,
mondo:0011538,frontoocular syndrome,['frontoocular syndrome'],,605321,,C1854405,,,,C565340,,,,
mondo:0011539,nemaline myopathy 5,"['nemaline myopathy caused by mutation in TNNT1', 'TNNT1 nemaline myopathy', 'nemaline myopathy, caused by mutation in the troponin t1 gene', 'NEM5', 'ANM', 'nemaline myopathy 5', 'nemaline myopathy, Amish type', 'nemaline myopathy type 5', 'nemaline myopathy 5, Amish type', 'Amish nemaline myopathy']",0110936,605355,98902,C1854380,"['-0.2036', '0.2502', '-0.2708', '0.05585', '0.1753', '-0.7676', '-0.1287', '0.534', '-0.554', '-0.225', '-0.1936', '0.1777', '0.0221', '0.00534', '0.0557', '0.3137', '-0.08295', '-0.3442', '-0.2272', '-0.4277', '-0.115', '0.015305', '0.0984', '-0.2822', '0.00787', '0.0656', '-0.2054', '-0.01874', '-0.2253', '-0.1449', '0.2284', '-0.03882', '0.2737', '0.2294', '0.234', '-0.294', '-0.0792', '-0.446', '-0.2305', '-0.1433', '-0.03235', '-0.3008', '-0.04666', '0.02306', '-0.1514', '0.1548', '-0.298', '0.5654', '-0.2444', '0.01802', '-0.10876', '-0.2277', '-0.0956', '-0.1592', '-0.03738', '-0.4153', '0.4487', '-0.2457', '0.1508', '0.09076', '0.3499', '-0.1442', '-0.02107', '0.0651', '-0.4268', '-0.0118', '0.4841', '0.2457', '-0.3455', '0.1514', '0.1061', '0.04877', '0.3096', '0.1562', '0.2996', '0.2534', '-0.2231', '-0.217', '-0.4978', '-0.2808', '0.2369', '0.281', '0.0784', '0.2242', '0.1417', '0.5254', '-0.1895', '0.4062', '0.316', '-0.1663', '0.4697', '0.2864', '0.1797', '0.003626', '0.497', '0.0931', '0.1888', '-0.1729', '0.12115', '-0.2668']",,,C538397,,,,
mondo:0011540,spinocerebellar ataxia type 14,"['spinocerebellar ataxia 14', 'spinocerebellar ataxia type 14', 'SCA14']",0050964,605361,98763,C4304883,"['-0.1481', '-0.0265', '-0.1539', '0.11884', '-0.2429', '-0.835', '0.2323', '0.3376', '-0.6055', '-0.8945', '0.1573', '0.2275', '-0.3079', '0.174', '0.544', '-0.3735', '-0.2471', '-0.6025', '0.0793', '-0.572', '-0.2412', '-0.2998', '0.222', '-0.514', '0.3525', '-0.5293', '-0.3516', '0.05673', '-0.1837', '-0.773', '0.0822', '0.3457', '-0.4722', '-0.1517', '0.4788', '0.0675', '-0.01869', '0.2162', '0.472', '0.5864', '0.159', '0.1203', '-0.58', '0.2852', '0.6934', '-0.525', '0.0788', '0.3699', '0.1796', '0.0918', '-0.0954', '-0.04373', '-0.04062', '-0.3853', '-0.027', '-0.702', '0.5835', '0.3196', '0.02432', '0.3875', '-0.709', '0.1888', '0.2281', '-0.1393', '-0.2917', '0.4905', '0.2222', '0.4326', '-0.4167', '0.4385', '0.683', '0.4495', '-0.00989', '-0.3994', '0.782', '0.3992', '0.1049', '0.1586', '0.1236', '0.616', '-0.1108', '-0.839', '0.428', '0.594', '-0.1953', '-0.5874', '0.266', '0.002062', '0.6777', '0.4167', '0.2588', '0.4746', '-0.02481', '0.01483', '0.9414', '0.943', '0.4758', '0.499', '-0.3071', '-0.07263']",,,C537196,,,,
mondo:0011541,dilated cardiomyopathy 1J,"['neurosensory deafness with dilated cardiomyopathy', 'dilated cardiomyopathy type 1J', 'sensorineural hearing loss with dilated cardiomyopathy', 'cardiomyopathy, dilated, type 1J', 'cardiomyopathy, dilated, 1J', 'familial dilated cardiomyopathy caused by mutation in EYA4', 'autosomal dominant dilated cardiomyopathy with sensorineural hearing loss', 'EYA4 familial dilated cardiomyopathy', 'neurosensory hearing loss with dilated cardiomyopathy', 'CMD1J', 'sensorineural deafness with dilated cardiomyopathy', 'cardiomyopathy, dilated, with sensorineural hearing loss, autosomal dominant']",0110440,605362,217622,C1854368,"['0.4038', '-0.703', '-0.05902', '0.6157', '0.05325', '-0.682', '0.6294', '0.736', '-0.1771', '-0.5293', '0.385', '-0.3252', '-0.305', '0.347', '-0.6494', '0.2732', '-0.8516', '0.01538', '-0.6445', '-0.7153', '0.1427', '0.3352', '0.4998', '-0.1515', '0.373', '-0.1776', '0.03677', '0.2637', '0.00938', '-0.399', '0.78', '-0.1112', '0.4143', '0.4856', '0.11005', '-0.6025', '-0.3096', '-0.5537', '0.74', '-0.557', '0.04514', '0.6357', '-0.02109', '0.533', '0.337', '0.3987', '0.2048', '0.7197', '0.4956', '-0.549', '-0.2255', '0.1901', '0.7485', '-0.1725', '0.625', '-0.574', '-0.4216', '0.2306', '-0.679', '-0.1573', '-0.2498', '0.593', '0.2524', '-0.929', '-1.039', '0.3472', '0.06995', '0.548', '-0.781', '0.06793', '-0.3862', '0.432', '0.0611', '-0.4744', '-0.1131', '0.65', '-0.1963', '0.0839', '-0.4512', '0.622', '0.10614', '-0.3396', '-0.1456', '-0.423', '1.24', '-0.1343', '0.5503', '0.0985', '0.5396', '0.6206', '0.3293', '0.2194', '-0.1567', '0.3677', '1.017', '1.064', '0.2365', '-0.5454', '-0.2588', '-0.2883']",,,C565337,,,,
mondo:0011542,"psoriasis 6, susceptibility to","['PSORS6', 'psoriasis susceptibility 6', 'psoriasis 6, susceptibility to']",0111290,605364,,,,,,,,,,
mondo:0011544,paragangliomas 3,"['paragangliomas 3', 'glomus tumors, familial, 3', 'PGL3', 'SDHC-related hereditary paraganglioma-pheochromocytoma syndrome (paragangliomas 3)', 'SDHC paraganglioma', 'paragangliomas type 3', 'paraganglioma caused by mutation in SDHC']",,605373,,C1854336,,,,C565335,,,,
mondo:0011545,autosomal dominant nocturnal frontal lobe epilepsy 3,"['epilepsy, nocturnal frontal lobe, 3', 'autosomal dominant nocturnal frontal lobe epilepsy type 3', 'epilepsy, nocturnal frontal lobe, type 3', 'ENFL3', 'CHRNB2 autosomal dominant nocturnal frontal lobe epilepsy', 'nocturnal frontal lobe epilepsy 3', 'autosomal dominant nocturnal frontal lobe epilepsy caused by mutation in CHRNB2']",0060684,605375,,C1854335,,,,C565334,,,,
mondo:0011546,"heterotaxy, visceral, 2, autosomal","['HTX2', 'heterotaxy, visceral, 2, autosomal', 'transposition of the great arteries, dextro-looped 2', 'Htx', 'DTGA2']",,605376,,C1415817,,,,,,,,
mondo:0011547,cataract 31 multiple types,"['early-onset non-syndromic cataract caused by mutation in CHMP4B', 'posterior polar cataract 3', 'CTRCT31', 'CTPP3', 'cataract, posterior polar, 3', 'CPP3', 'cataract 31, multiple types', 'CHMP4B early-onset non-syndromic cataract']",0110265,605387,98993,,,,,C535343,,,,
mondo:0011548,"cerebral palsy, ataxic, autosomal recessive","['ataxic cerebral palsy', 'Acp', 'cerebral palsy, ataxic, autosomal recessive', 'cerebral palsy ataxic']",,605388,,,,,,,343.8,,,
mondo:0011549,hypotrichosis 1,"['HYPT1', 'hypotrichosis 1', 'hypotrichosis caused by mutation in APCDD1', 'hereditary generalised hypotrichosis simplex', 'HTS', 'APCDD1 hypotrichosis', 'hereditary generalized hypotrichosis simplex', 'hypotrichosis type 1', 'hypotrichosis simplex, generalized, hereditary', 'HHS']",0110698,605389,,,,,,,,,,
mondo:0011550,"fibromatosis, gingival, with hypertrichosis and intellectual disability","['fibromatosis, gingival, with hypertrichosis and mental retardation', 'fibromatosis, gingival, with hypertrichosis and intellectual disability']",,605400,,C1854306,,,,C565331,,,,
mondo:0011551,TH-deficient dopa-responsive dystonia,"['DYT5b', 'Parkinsonism, infantile, autosomal recessive', 'autosomal recessive dopa-responsive dystonia', 'dystonia, DOPA responsive, autosomal recessive', 'Segawa syndrome, autosomal recessive', 'tyrosine hydroxylase-deficient dopa-responsive dystonia', 'Segawa syndrome, recessive', 'DOPA responsive dystonia, autosomal recessive', 'dopa-responsive dystonia, autosomal recessive', 'Dopa-responsive dystonia, autosomal recessive', 'autosomal recessive Segawa syndrome', 'dystonia, Dopa-responsive, autosomal recessive']",,605407,101150,C2673535,"['0.555', '0.2878', '-0.2035', '-0.2812', '-0.035', '-0.659', '0.10956', '0.02957', '-0.664', '-0.3994', '0.7393', '0.749', '-0.06757', '0.6177', '0.3987', '0.5366', '-0.2161', '-0.7817', '-0.3328', '-0.8115', '-0.1466', '-0.009735', '0.08185', '-0.2007', '-0.691', '0.2078', '0.1273', '-0.1879', '-0.288', '0.09534', '0.1371', '0.366', '0.7505', '0.0983', '-0.06088', '-0.0848', '0.2957', '-0.04758', '0.1814', '-0.3447', '0.532', '-0.3572', '-0.2152', '0.1313', '0.633', '-0.2167', '-0.4119', '-0.04596', '0.005074', '0.713', '0.1437', '0.0937', '0.3027', '-0.35', '0.5923', '0.1816', '0.1433', '0.4163', '0.436', '-0.1154', '-0.561', '-0.2181', '0.05865', '-0.8037', '-0.54', '0.4614', '0.1054', '-0.05664', '-0.2935', '0.4097', '-0.0837', '-0.21', '0.473', '-0.01732', '0.439', '0.621', '0.7134', '-0.389', '0.2499', '-0.00882', '0.006924', '-0.02333', '0.548', '0.544', '0.917', '0.6167', '0.287', '0.2874', '1.36', '0.2148', '0.5166', '0.2174', '-0.2954', '0.2369', '1.051', '0.0999', '-0.0692', '-0.348', '0.807', '-0.731']",,,,,,,
mondo:0011552,schizophrenia 10,"['schizophrenia susceptibility locus, chromosome 15Q15-related', 'SCZD10', 'catatonia, periodic', 'schizophrenia 10']",0070086,605419,,,,,,D012560,,,,
mondo:0011553,autosomal recessive nonsyndromic hearing loss 26,"['autosomal recessive nonsyndromic deafness type 26', 'deafness, autosomal recessive 26', 'DFNB26', 'autosomal recessive deafness 26', 'autosomal recessive nonsyndromic deafness 26']",0110484,605428,,C1854275,,,,C565329,,,,
mondo:0011555,radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome,"['RUSAT', 'radioulnar synostosis with amegakaryocytic thrombocytopenia', 'ATRUS syndrome']",,,71289,,"['-0.08405', '-0.0775', '0.10223', '-0.1736', '0.4363', '-0.5356', '-0.1056', '0.5796', '-0.2263', '-0.918', '-0.2202', '-0.05557', '-0.1265', '-0.00525', '0.05225', '-0.06824', '0.07947', '0.04767', '-0.1013', '-0.2693', '0.10803', '-0.0552', '0.000175', '-0.371', '0.602', '0.309', '0.006584', '-0.0728', '0.3684', '0.1232', '-0.1877', '-0.366', '0.0895', '-0.01881', '0.169', '-0.3887', '0.02925', '-0.5923', '0.0712', '-0.1252', '-0.4', '-0.3972', '0.2642', '-0.4365', '0.12067', '-0.3674', '-0.3545', '0.319', '0.00811', '-0.396', '0.136', '-0.3726', '-0.07446', '0.0871', '-0.345', '-0.3662', '0.6025', '-0.0164', '-0.4314', '-0.0655', '0.3542', '0.1349', '0.0571', '-0.1584', '0.004757', '-0.448', '-0.10596', '0.501', '-0.3982', '0.05475', '-0.3967', '0.1588', '0.05847', '-0.122', '0.4058', '0.4429', '0.1267', '0.148', '-0.2732', '-0.2922', '0.04025', '0.4802', '0.3489', '0.4583', '-0.0845', '0.2086', '0.1009', '0.701', '-0.2595', '-0.1396', '0.1537', '0.3364', '0.2473', '-0.1256', '0.8613', '0.1432', '0.856', '-0.9546', '0.2228', '-0.11505']",,,C565328,,,,
mondo:0011556,"basal cell carcinoma, susceptibility to, 1","['basal cell carcinoma, susceptibility to, 1', 'BCC1', 'basal cell carcinoma, nonsyndromic', 'multiple basal cell carcinoma', 'basal cell carcinoma, multiple', 'basal cell carcinoma, somatic']",,605462,,,,,,,,,,
mondo:0011557,"radiation sensitivity/chromosome instability syndrome, autosomal dominant","['radiation sensitivity/chromosome instability syndrome, autosomal dominant']",,605463,,C1854244,,,,C565326,,,,
mondo:0011558,Usher syndrome type 2C,"['USHER syndrome, type IIC', 'Usher syndrome, type IIb', 'Usher syndrome, type 2C, autosomal recessive, digenic dominant', 'Usher syndrome, type IIc, Gpr98/Pdzd7, digenic', 'Usher syndrome, type 2C', 'Usher syndrome, type IIb, formerly', 'Usher syndrome type IIC', 'Usher syndrome, type IIC, GPR98/PDZD7 digenic, autosomal recessive, digenic dominant', 'USH2C', 'Usher syndrome, type 2C, GPR98/PDZD7 digenic, autosomal recessive, digenic dominant']",0110839,605472,,,,C153174,,C536492,,H35.5,,
mondo:0011559,benign recurrent intrahepatic cholestasis type 2,"['BRIC2', 'Bric type 2', 'recurrent familial intrahepatic cholestasis 2', 'cholestasis, benign recurrent intrahepatic, type 2', 'cholestasis, benign recurrent intrahepatic, 2', 'mild ABCB11 deficiency', 'cholestasis, benign recurrent intrahepatic 2', 'benign recurrent intrahepatic cholestasis 2']",0070232,605479,99961,,"['-0.1161', '0.0861', '0.04327', '-0.07404', '0.03552', '-0.0925', '0.1106', '0.137', '-0.12274', '0.10205', '-0.2246', '-0.09485', '-0.05026', '0.0839', '-0.1866', '-0.2263', '0.071', '-0.03543', '0.001646', '-0.2537', '-0.05954', '-0.1724', '0.2384', '-0.02391', '-0.04196', '-0.0873', '0.0334', '-0.002348', '-0.0698', '-0.0648', '0.2341', '0.05417', '0.10956', '0.11957', '-0.1173', '-0.1711', '-0.0543', '-0.02707', '-0.01461', '-0.0783', '0.05957', '-0.1295', '0.148', '0.0637', '-0.07495', '0.00396', '0.03084', '0.0664', '0.0295', '0.04202', '-0.009415', '-0.009346', '0.1152', '-0.04996', '-0.11395', '-0.05472', '0.04633', '-0.1747', '-0.2416', '0.04654', '0.1432', '0.1598', '0.1057', '-0.08026', '0.1272', '-0.009056', '0.2795', '0.1218', '-0.2666', '0.1287', '-0.0556', '0.01807', '0.12036', '-0.214', '0.10657', '0.05353', '0.1115', '0.04355', '-0.1047', '-0.0855', '-0.0805', '-0.02797', '-0.1243', '0.00792', '-0.0891', '-0.02095', '0.0841', '0.02245', '0.2017', '-0.1493', '0.1561', '0.2288', '-0.0712', '-0.03162', '0.375', '0.06616', '0.141', '-0.238', '-0.11273', '0.1028']",,,C535934,,,,
mondo:0011560,"systemic lupus erythematosus, susceptibility to, 3","['SLEB3', 'systemic lupus erythematosus, susceptibility to, 3']",,605480,,,,,,,,,,
mondo:0011561,Alzheimer disease 6,"['Alzheimer^s disease type 6', 'Alzheimer^s disease 6', 'AD6', 'Alzheimer disease 6', 'Alzheimer disease 6, late onset', 'Alzheimer disease type 6', 'Alzheimer disease 6, late-onset', 'plasma Beta-amyloid-42 level quantitative trait locus']",0110038,605526,,,,,,C565325,,,,
mondo:0011562,autosomal dominant Parkinson disease 4,"['autosomal dominant Parkinson^s disease 4', 'autosomal dominant Lewy body Parkinson disease 4', 'PARK4', 'autosomal dominant Parkinson disease type 4', 'Parkinson disease 4, autosomal dominant', 'Parkinson disease 4, autosomal dominant Lewy body']",0060895,605543,,C1854182,,,,C565324,,,,
mondo:0011563,"fibromatosis, gingival, 2","['gingival fibromatosis, 2', 'fibromatosis, gingival, 2', 'fibromatosis, gingival, hereditary, 2', 'GINGF2', 'GGF2', 'HGF2', 'fibromatosis gingival, hereditary, 2', 'hereditary gingival fibromatosis, 2']",,605544,,,,,,C565323,,,,
mondo:0011564,cone-rod dystrophy 8,"['CORD8', 'cone-rod dystrophy 8', 'cone-rod dystrophy type 8']",0111014,605549,,C1854180,,,,C565322,,,,
mondo:0011565,metabolic syndrome X,"['abdominal obesity-metabolic syndrome quantitative trait locus 1', 'metabolic syndrome 10', 'abdominal obesity-metabolic syndrome 1', 'metabolic syndrome type X', 'AOMS1', 'abdominal obesity metabolic syndrome', 'dysmetabolic syndrome X', 'metabolic syndrome, protection against']",14221,605552,,C0524620,,,,D024821,277.7,,,
mondo:0011566,abdominal obesity-metabolic syndrome quantitative trait locus 2,"['Abdominal obesity-metabolic syndrome', 'Aoms2', 'abdominal obesity-metabolic syndrome quantitative trait locus type 2', 'abdominal obesity-metabolic syndrome quantitative trait locus 2']",,605572,,,,,,,,,,
mondo:0011567,dilated cardiomyopathy 1K,"['cardiomyopathy, dilated, 1K', 'dilated cardiomyopathy type 1K', 'CMD1K']",0110437,605582,,C1854159,,,,C565320,,,,
mondo:0011568,autosomal dominant nonsyndromic hearing loss 25,"['autosomal dominant nonsyndromic deafness 25', 'autosomal dominant nonsyndromic deafness type 25', 'deafness, autosomal dominant 25', 'deafness, autosomal dominant type 25', 'autosomal dominant nonsyndromic deafness caused by mutation in SLC17A8', 'DFNA25', 'autosomal dominant deafness 25', 'SLC17A8 autosomal dominant nonsyndromic deafness']",0110555,605583,,C1854158,,,,C565319,,,,
mondo:0011569,Charcot-Marie-Tooth disease type 2B1,"['Charcot-Marie-Tooth disease, type 2B1', 'Charcot-Marie-Tooth disease, neuronal, type 2B1', 'Charcot-Marie-Tooth disease type 2 caused by mutation in LMNA', 'Charcot Marie Tooth disease type 2B1', 'AR-CMT2B1', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, 2B1', 'CMT2B1', 'Charcot-Marie-Tooth disease neuronal type 2B1', 'autosomal recessive Charcot-Marie-Tooth disease type 2B1', 'CMT 2B1', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2B1', 'Charcot-Marie-Tooth neuropathy, type 2B1', 'Charcot-Marie-Tooth disease, axonal, type 2B1', 'autosomal recessive axonal CMT4C1', 'autosomal recessive axonal Charcot-Marie-Tooth disease type 2B1', 'LMNA Charcot-Marie-Tooth disease type 2', 'Charcot-Marie-Tooth neuropathy type 2B1']",0110156,605588,98856,C1854154,"['0.1444', '0.4553', '0.00549', '-0.02228', '-0.1174', '-0.1777', '-0.2808', '0.751', '-0.754', '-0.129', '-0.0726', '0.1316', '-0.1865', '0.0925', '0.011444', '-0.449', '-0.4814', '-0.587', '-0.1918', '-0.7817', '0.04987', '0.033', '0.5444', '0.4192', '0.3613', '0.4443', '-0.09344', '0.1666', '-0.01411', '-0.1399', '0.1164', '-0.8394', '-0.1947', '-0.01284', '0.2937', '-0.897', '-0.4475', '-0.325', '0.3525', '-0.3237', '-1.698', '-0.3667', '-0.444', '0.4004', '-0.1539', '-0.07556', '-0.09674', '-0.3113', '-0.286', '0.01173', '0.11633', '0.3115', '-0.004734', '-0.837', '0.5083', '-0.1663', '0.0347', '0.3782', '-0.3843', '-0.1346', '-0.28', '0.02705', '0.767', '0.88', '-1.09', '1.081', '-0.0947', '0.9683', '-0.525', '0.44', '-0.6733', '0.11816', '0.504', '-0.2263', '1.052', '0.7847', '-0.3894', '0.4827', '0.5522', '-0.2399', '-0.2128', '0.0651', '0.8164', '0.7935', '-0.06824', '-0.2096', '0.2145', '0.4932', '0.7144', '-0.03983', '0.1522', '-0.10394', '0.08844', '0.3276', '0.434', '0.3274', '0.3975', '-0.6', '-0.2737', '0.146']",,,C537990,,,,
mondo:0011570,Charcot-Marie-Tooth disease type 2B2,"['AR-CMT2B2', 'CMT2B2', 'CMT 2B2', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2B2', 'Charcot-Marie-Tooth disease, type 2B2', 'autosomal recessive axonal Charcot-Marie-Tooth disease type 2B2', 'ARCMT2B', 'Charcot-Marie-Tooth disease, axonal, type 2B2', 'Charcot-Marie-Tooth neuropathy, type 2B2', 'Arcmt2B', 'MED25 Charcot-Marie-Tooth disease type 2', 'Charcot-Marie-Tooth disease, neuronal, type 2B2', 'Charcot-Marie-Tooth disease neuronal type 2B2', 'Charcot Marie Tooth disease type 2B2', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, B2', 'Charcot-Marie-Tooth disease type 2 caused by mutation in MED25', 'Charcot-Marie-Tooth neuropathy type 2B2', 'autosomal recessive axonal CMT4C3']",0110179,605589,101101,C1854150,"['-0.0413', '0.4976', '0.0598', '0.1354', '-0.0599', '0.0674', '-0.4514', '0.7505', '-0.6504', '-0.2006', '-0.03079', '0.248', '-0.4377', '0.2551', '0.010826', '-0.215', '-0.1488', '-0.2607', '-0.4392', '-0.6514', '0.01126', '0.1032', '0.3125', '0.4124', '0.1931', '0.66', '-0.0696', '0.3896', '0.1026', '-0.402', '-0.01935', '-0.9067', '-0.03008', '0.2585', '0.3757', '-0.94', '-0.471', '-0.4946', '0.2874', '-0.1818', '-1.802', '-0.42', '-0.6147', '0.3164', '-0.0475', '-0.1257', '0.03192', '-0.1548', '-0.1427', '-0.06494', '0.0482', '0.3198', '-0.2983', '-0.946', '0.4092', '-0.05136', '-0.00125', '0.2208', '-0.367', '0.1926', '-0.4722', '0.01762', '0.7285', '0.9526', '-1.122', '1.086', '-0.1469', '0.8135', '-0.735', '0.6177', '-0.5723', '0.3481', '0.3704', '-0.1565', '1.396', '0.7495', '-0.3662', '0.603', '0.385', '-0.4817', '-0.2189', '0.008675', '0.807', '0.667', '0.1604', '-0.3547', '0.2695', '0.853', '0.8247', '0.0793', '0.2384', '-0.04108', '0.344', '0.3115', '0.4119', '0.537', '0.3691', '-0.6924', '-0.1146', '0.1416']",,,C537991,,,,
mondo:0011571,"deafness, autosomal dominant 39, with dentinogenesis imperfecta 1","['deafness, autosomal dominant 39, with dentinogenesis', 'deafness, autosomal dominant 39, with dentinogenesis imperfecta 1', 'Dgi1/Dfna39 syndrome', 'Dfna39/Dgi1 syndrome', 'deafness, autosomal dominant 39, with dentinogenesis imperfecta type 1', 'Dfna39/dentinogenesis imperfecta 1 syndrome']",,605594,,C1854146,"['-0.00572', '0.062', '0.01698', '-0.02644', '0.06006', '-0.0925', '0.008705', '0.1066', '-0.04742', '-0.0309', '-0.02478', '-0.01915', '-0.02927', '-0.0005655', '0.005203', '-0.03818', '0.01689', '-0.03268', '-0.01374', '-0.1237', '-0.03128', '-0.0224', '0.08356', '-0.02583', '0.01785', '-0.00682', '-0.02403', '-0.0323', '-0.0088', '-0.0488', '0.0631', '-0.002512', '0.05774', '0.0469', '0.01082', '-0.044', '-0.01248', '-0.05838', '-0.015335', '-0.0797', '0.04764', '-0.0916', '0.02638', '-0.0278', '-0.0315', '-0.07574', '-0.0183', '0.08374', '0.02893', '0.03107', '0.02112', '-0.04636', '0.02159', '-0.005188', '-0.03537', '-0.04135', '0.08685', '-0.0443', '-0.089', '0.01047', '0.05435', '0.0159', '0.00806', '-0.004234', '0.00458', '-0.01218', '0.07275', '0.0737', '-0.0798', '0.10944', '-0.0505', '0.003399', '0.01428', '-0.0905', '0.05933', '0.05542', '-0.00668', '0.006718', '-0.05887', '-0.04263', '0.0002935', '-0.0174', '-0.02051', '0.07196', '-0.03128', '0.02875', '0.02722', '0.09326', '0.08777', '0.0233', '0.021', '0.069', '-0.00489', '0.02774', '0.1802', '0.02325', '0.09674', '-0.10944', '-0.01749', '0.02063']",,,C565316,,,,
mondo:0011572,type 1 diabetes mellitus 18,"['IDDM18', 'insulin-dependent diabetes mellitus 18', 'diabetes mellitus, insulin-dependent, 18']",0110755,605598,,C1854125,,,,C565315,,,,
mondo:0011573,"psoriasis 7, susceptibility to","['psoriasis 7, susceptibility to', 'psoriasis susceptibility 7', 'PSORS7', 'psoriasis, protection against']",0111279,605606,,,,,,,,,,
mondo:0011574,"tetralogy of fallot syndrome, autosomal recessive","['tetralogy of fallot syndrome, autosomal recessive']",,605618,,C1854119,,,,C565314,,,,
mondo:0011575,cerebrooculonasal syndrome,['cerebrooculonasal syndrome'],,605627,66625,C1854108,,,,C565313,,,,
mondo:0011576,familial hyperaldosteronism type II,"['FH2', 'HALD2', 'familial adrenal adenoma', 'FH 2', 'FHII', 'familial hyperaldosteronism type 2', 'FH-II', 'hyperaldosteronism, familial, type II']",,605635,404,C3839212,"['-0.2241', '0.262', '-0.421', '-0.1707', '-0.1453', '-0.2773', '0.3203', '0.03275', '-0.2349', '-0.3792', '-0.415', '-0.1603', '0.05966', '0.4265', '-0.7456', '-0.5933', '-0.4626', '-0.08673', '0.6846', '-0.851', '0.0769', '-0.2634', '0.3926', '-0.4727', '-0.0385', '0.3318', '0.09503', '-0.01869', '0.7954', '0.10266', '0.4856', '-0.0992', '0.709', '0.1053', '-0.683', '-0.5654', '-0.4065', '0.0286', '0.1655', '-0.02519', '-0.1018', '-0.347', '0.868', '-0.3645', '0.1299', '0.523', '0.1008', '-0.1349', '-0.2515', '0.4485', '0.2389', '-0.11035', '-0.01755', '-0.59', '-0.3926', '-0.1517', '0.358', '-0.8755', '-0.1646', '0.6274', '-0.085', '0.1191', '0.1742', '-0.5674', '-0.525', '0.503', '0.3533', '0.37', '-0.219', '0.1534', '-0.10406', '-0.1871', '0.10803', '-0.6045', '0.625', '0.5044', '-0.0731', '-0.08246', '-0.2993', '-0.2515', '-0.1758', '0.5225', '-0.0214', '-0.2456', '0.42', '0.006645', '0.5166', '-0.1682', '0.1686', '0.0325', '-0.0977', '-0.0653', '0.015465', '-0.4001', '1.106', '-0.09155', '0.9033', '-0.26', '-0.6987', '-0.225']",C127162,,C565312,,,,
mondo:0011577,"myopathy, proximal, and ophthalmoplegia","['MYPOP', 'proximal myopathy and ophthalmoplegia', 'MYOPATHY, proximal, and ophthalmoplegia', 'inclusion body myopathy 3, autosomal dominant, formerly', 'inclusion body myopathy 3, autosomal dominant', 'myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles', 'myopathy, proximal, and ophthalmoplegia']",0080719,605637,,C1854106,"['-0.0374', '0.03677', '0.0186', '-0.02803', '0.0109', '-0.0767', '0.00803', '0.0678', '-0.08105', '-0.03317', '-0.01526', '0.00906', '0.007126', '0.02078', '-0.010124', '-0.0231', '0.0047', '-0.01898', '-0.02383', '-0.11053', '0.00853', '-0.0408', '0.04547', '0.00568', '0.0002202', '-0.02086', '0.000701', '-0.005787', '-0.02426', '-0.02377', '0.0367', '0.0004518', '0.04797', '0.00995', '0.01034', '-0.0329', '-0.013756', '-0.02615', '-0.01938', '-0.0456', '0.003252', '-0.0676', '-9.555e-05', '0.00833', '0.00443', '-0.03253', '-0.03473', '0.0429', '-0.008385', '0.02696', '-0.02061', '0.00788', '0.01949', '-0.00966', '-0.0215', '-0.04807', '0.0596', '-0.0403', '-0.0803', '-0.004967', '0.0472', '0.000983', '0.0182', '0.007607', '-0.0404', '0.00137', '0.05063', '0.06396', '-0.04407', '0.0601', '-0.05515', '0.01197', '0.0325', '-0.01237', '0.0383', '0.02051', '0.01339', '-0.006336', '-0.02618', '-0.04416', '0.004353', '0.003624', '0.007618', '0.05722', '-0.01762', '0.0303', '-0.001362', '0.0602', '0.0489', '-0.0188', '0.02899', '0.04453', '0.00864', '0.01527', '0.09143', '0.028', '0.06335', '-0.05106', '-0.01855', '0.00366']",,,C565311,,,,
mondo:0011578,familial papillary thyroid carcinoma with renal papillary neoplasia,"['ptc-RCC', 'Prn1', 'thyroid carcinoma, papillary, with papillary renal neoplasia', 'Ptcprn']",,605642,97290,C1854104,,,,C565310,,,,
mondo:0011579,late-onset retinal degeneration,"['retinal Degeneration, late-onset, autosomal dominant', 'autosomal dominant late-onset retinal degeneration', 'LORD', 'pigmentary retinopathy', 'late-onset retinal degeneration']",0060869,605670,67042,C1854065,"['-0.6577', '-0.2499', '0.0743', '-0.144', '0.04037', '-0.2117', '-0.3455', '0.4214', '-0.432', '-0.3914', '-0.3643', '0.132', '-0.2722', '0.3877', '-0.459', '-0.483', '-0.06006', '-0.4905', '0.2013', '-0.6426', '0.3762', '-0.3591', '-0.01241', '0.2957', '0.1074', '-0.012474', '-0.10205', '-0.063', '-0.1713', '0.4788', '0.6255', '0.02498', '-0.3867', '0.2876', '0.09735', '0.4846', '0.1237', '-0.08636', '-0.09576', '-0.379', '0.465', '-0.0662', '0.2815', '0.2479', '-0.3147', '-0.10706', '0.1685', '-0.1427', '0.02553', '0.3186', '0.496', '0.268', '-0.00881', '-0.271', '0.2727', '-0.589', '1.112', '-0.02866', '-0.5327', '0.293', '0.2051', '0.1422', '-0.3862', '0.4094', '-0.0424', '0.02274', '0.7485', '0.9204', '0.129', '0.5293', '-0.3828', '0.0687', '0.4355', '-0.1337', '-0.1581', '-0.2186', '0.01726', '-0.04004', '0.0694', '-0.0349', '0.551', '-0.233', '0.01767', '0.5366', '-0.227', '-0.3506', '0.03018', '-0.1826', '0.3567', '0.1957', '0.08905', '0.4883', '0.1434', '0.2896', '0.561', '-0.001487', '0.438', '-0.1143', '-0.004066', '0.0822']",,,C565309,,,,
mondo:0011580,cerebellar ataxia and hypergonadotropic hypogonadism,['cerebellar ataxia and hypergonadotropic hypogonadism'],,605672,,C1854064,,,,C565308,,,,
mondo:0011581,arrhythmogenic cardiomyopathy with wooly hair and keratoderma,"['woolly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome', 'DCWHK', 'cardiomyopathy dilated with woolly hair and keratoderma', 'keratoderma with wooly hair type II', 'cardiomyopathy, dilated, with woolly hair and keratoderma', 'palmoplantar keratoderma with left ventricular cardiomyopathy and wooly hair', 'cardiomyopathy dilated with wooly hair and keratoderma', 'palmoplantar keratoderma with left ventricular cardiomyopathy and woolly hair', 'keratoderma with woolly hair type II', 'cardiomyopathy, dilated, with wooly hair and keratoderma', 'wooly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome', 'wooly hair - palmoplantar keratoderma - dilated cardiomyopathy syndrome', 'Carvajal syndrome', 'KWWH type II', 'dilated cardiomyopathy with wooly hair and keratoderma', 'woolly hair - palmoplantar keratoderma - dilated cardiomyopathy', 'wooly hair - palmoplantar keratoderma - dilated cardiomyopathy', 'wooly hair-palmoplantar hyperkeratosis-dilated cardiomyopathy syndrome', 'woolly hair - palmoplantar keratoderma - dilated cardiomyopathy syndrome', 'epidermolytic palmoplantar keratoderma wooly hair and dilated cardiomyopathy', 'woolly hair-palmoplantar keratoderma-dilated cardiomyopathy syndrome', 'epidermolytic palmoplantar keratoderma woolly hair and dilated cardiomyopathy', 'dilated cardiomyopathy with woolly hair and keratoderma']",0090128,605676,65282,C1854063,"['0.2615', '-0.4314', '-0.1473', '0.3643', '-0.11316', '-0.7217', '0.1652', '0.478', '-0.0003803', '-0.4604', '0.246', '-0.1703', '-0.1991', '0.3655', '-0.5815', '0.4238', '-0.692', '-0.1847', '-0.4033', '-0.6895', '0.0517', '0.507', '0.7446', '-0.2732', '0.558', '0.1351', '0.2004', '0.5156', '-0.217', '-0.5293', '0.9536', '-0.335', '0.446', '0.5654', '0.08923', '-0.3242', '0.09503', '-0.1228', '0.6753', '-0.3972', '0.02208', '0.5913', '0.09644', '0.2522', '0.1805', '0.2656', '0.1818', '0.672', '0.2192', '-0.6274', '-0.3428', '0.1292', '0.7354', '0.1162', '0.7466', '-0.4802', '-0.2957', '0.3262', '-0.744', '-0.1664', '-0.1484', '0.6084', '0.079', '-0.9595', '-0.6147', '0.1503', '0.2229', '0.43', '-0.7954', '0.06946', '-0.452', '0.05777', '-0.1108', '-0.1628', '0.0701', '0.639', '-0.366', '-0.2793', '-0.1071', '0.38', '0.08453', '-0.296', '0.0591', '-0.419', '1.138', '-0.3972', '0.5166', '0.1715', '0.466', '0.11035', '0.3992', '-0.06165', '-0.0184', '0.346', '0.8955', '0.6875', '0.05914', '-0.6343', '-0.02744', '-0.05704']",,,C535581,,,,
mondo:0011582,multiple mitochondrial dysfunctions syndrome 1,"['multiple mitochondrial dysfunctions syndrome 1', 'fatal multiple mitochondrial dysfunctions syndrome caused by mutation in NFU1', 'NFU1 fatal multiple mitochondrial dysfunctions syndrome', 'Mmds', 'NFU1 deficiency', 'multiple mitochondrial dysfunctions syndrome type 1', 'MMDS1']",0080133,605711,401869,CN226135,"['-0.287', '0.1356', '-0.1202', '-0.2769', '-0.0988', '-0.726', '0.2837', '0.2776', '-0.4329', '0.113', '-0.2852', '-0.252', '0.0234', '-0.3345', '0.1247', '-0.2627', '-0.2338', '0.023', '-0.2603', '-0.5977', '0.3037', '-0.2578', '0.3105', '-0.2222', '0.09296', '-0.2345', '0.1891', '0.2372', '0.03442', '0.0474', '0.3604', '0.1614', '0.6895', '0.1952', '0.0873', '-0.1732', '0.03265', '-0.1147', '-0.000996', '0.1292', '0.07043', '-0.2228', '0.2695', '0.3135', '-0.1752', '0.01386', '-0.2037', '0.2725', '-0.1733', '0.003862', '-0.3115', '0.1126', '0.1063', '-0.08997', '-0.10254', '-0.1877', '0.1564', '0.03915', '0.007393', '0.5454', '0.0962', '0.0964', '0.3704', '-0.1829', '-0.328', '-0.1244', '0.385', '0.5654', '-0.4404', '0.3801', '-0.407', '0.11127', '0.02296', '-0.08014', '-0.156', '-0.1488', '0.1532', '-0.1128', '-0.2664', '0.31', '0.1307', '0.1216', '-0.05566', '0.1067', '0.2118', '-0.11957', '0.4175', '0.32', '0.2734', '0.1333', '0.518', '0.0905', '0.0796', '0.0885', '0.4783', '0.4636', '0.516', '-0.2163', '0.07635', '-0.1323']",,,,,,,
mondo:0011583,"cerebral amyloid angiopathy, APP-related","['cerebral amyloid angiopathy, APP-related, Dutch variant', 'cerebral amyloid angiopathy, APP-related, Iowa variant', 'amyloidosis, hereditary, with cerebral hemorrhage, Dutch variant', 'cerebral amyloid angiopathy, APP-related, Arctic variant', 'cerebral amyloid angiopathy, APP-related, Italian variant', 'cerebral amyloid angiopathy, APP-related', 'cerebral amyloid angiopathy, Dutch, Italian, Iowa, Flemish, Arctic variants', 'cerebral amyloid angiopathy, APP-related, Flemish variant', 'APP-related cerebral amyloid angiopathy', 'amyloidosis, Cerebroarterial, APP-related', 'HCHWAD']",0070028,605714,,C3888309,"['-0.003298', '0.07745', '0.01146', '-0.004745', '0.02567', '-0.06094', '-0.01088', '0.06024', '-0.0711', '-0.007587', '-0.0668', '-0.03342', '-0.0552', '-0.01068', '-0.0326', '-0.05234', '-0.03102', '-0.05136', '-0.00521', '-0.1178', '0.006428', '-0.012436', '0.05054', '-0.003683', '0.007465', '-0.0347', '-0.02264', '0.01176', '-0.01371', '-0.0249', '0.0361', '-0.01831', '0.12476', '0.003523', '0.01888', '-0.006115', '0.008995', '0.01599', '0.00543', '-0.0739', '0.0556', '-0.07806', '0.004177', '-0.01222', '0.0356', '-0.02676', '-0.013016', '0.05606', '0.02449', '0.0314', '0.02112', '0.039', '0.02234', '0.01111', '-0.0126', '0.003656', '0.05896', '-0.03041', '-0.07214', '0.02403', '0.02237', '0.03152', '0.002396', '-0.01923', '-0.008644', '0.002316', '0.0673', '0.0944', '-0.11084', '0.0828', '-0.06204', '0.02522', '0.01808', '-0.03696', '0.02989', '0.05267', '-0.00644', '0.04102', '-0.07574', '-0.07544', '-0.03102', '-0.04575', '-0.02907', '0.04968', '0.01227', '-0.01426', '0.01802', '0.0349', '0.07385', '-0.01188', '0.0449', '0.00795', '0.001972', '-0.02599', '0.09436', '0.03976', '0.04114', '-0.081', '0.01714', '0.0539']",C157147,,,,,,
mondo:0011584,Fanconi anemia complementation group D1,"['inherited cancer-predisposing syndrome due to biallelic BRCA2 mutations', 'Fanconi anemia, complementation group D1', 'FAD1', 'Fad1', 'FANCD1']",0111089,605724,319462,C1838457,"['-0.2834', '0.2898', '0.09674', '0.318', '0.6875', '0.1138', '-0.1776', '0.4229', '-0.3105', '-0.4143', '0.6465', '0.2314', '0.2161', '0.2465', '-1.071', '-0.1162', '-0.591', '0.2139', '-0.581', '-0.2474', '-0.1583', '-0.6084', '0.264', '-0.1621', '0.7446', '-0.438', '-0.01444', '-0.4055', '0.6255', '0.1401', '0.3965', '0.06696', '0.427', '0.5586', '0.648', '-0.1782', '-0.8413', '-0.377', '0.3557', '-0.3005', '-0.758', '0.1672', '0.1158', '-0.5645', '-0.4475', '-0.81', '0.10864', '0.1768', '0.5273', '-0.4646', '0.3586', '0.5435', '0.6255', '-0.0873', '0.43', '-0.58', '0.1041', '0.3154', '-0.933', '0.316', '-0.0452', '0.2908', '-0.2773', '-0.4187', '-0.1722', '0.4058', '0.2825', '0.7217', '-0.76', '1.079', '0.826', '-0.3782', '-0.391', '-0.4927', '0.3005', '0.9087', '0.1898', '0.3857', '0.1769', '0.266', '0.2732', '0.0127', '-0.01495', '0.1973', '0.1963', '-0.5054', '-0.3345', '0.303', '0.8945', '-0.1676', '0.4602', '0.4407', '-0.3425', '-0.2301', '0.3462', '1.075', '0.3809', '-0.07074', '0.1305', '-0.569']",C125705,,C563980,,,,
mondo:0011585,autosomal recessive distal spinal muscular atrophy 2,"['motor neuropathy, distal, Jerash type', 'HMNJ', 'distal hereditary motor neuropathy Jerash type', 'autosomal recessive distal spinal muscular atrophy type 2', 'spinal muscular atrophy Jerash type', 'neuronopathy, distal hereditary motor, Jerash type', 'neuropathy, distal hereditary motor, Jerash type', 'hereditary motor neuropathy, Jerash type', 'MNDJ', 'spinal muscular atrophy, distal, autosomal recessive, 2', 'dHMNJ', 'spinal muscular atrophy, distal, autosomal recessive, type 2', 'distal hereditary motor neuropathy, Jerash type', 'spinal muscular atrophy, Jerash type', 'DSMA2']",0111065,605726,139552,,"['-0.2793', '0.1835', '-0.1219', '0.01241', '-0.3987', '-0.773', '-0.1406', '1.032', '-1.263', '0.0963', '-0.2576', '0.05508', '-0.1727', '0.1361', '0.4048', '-0.03857', '0.2832', '-0.3606', '0.0696', '-0.677', '0.4114', '-0.01385', '0.5947', '0.05548', '0.0427', '0.2263', '-0.0485', '0.3599', '-0.881', '0.03635', '0.4849', '0.2761', '-0.0853', '0.4648', '-0.2515', '-0.284', '-0.542', '-0.1384', '-0.4937', '-0.279', '-0.506', '-0.3096', '-0.2156', '0.3284', '0.07574', '0.1448', '-0.4707', '0.554', '-0.1311', '0.5005', '-0.06586', '0.6787', '-0.2408', '-0.544', '-0.03555', '-0.5312', '0.2817', '-0.2081', '-0.7695', '0.3872', '-0.05347', '-0.01475', '-0.2466', '0.4387', '-0.8228', '0.1652', '0.473', '0.3813', '-0.1338', '0.455', '0.05627', '0.04675', '0.6436', '-0.1888', '0.703', '0.01211', '-0.0695', '0.5044', '-0.02498', '-0.2238', '-0.559', '-0.1266', '1.076', '0.2218', '-0.2554', '0.06274', '-0.1915', '0.2277', '0.1904', '-0.4048', '0.353', '0.02168', '-0.0452', '0.136', '0.3071', '0.287', '0.5186', '-0.1388', '-0.4497', '0.4614']",,,C535715,,,,
mondo:0011586,otosclerosis 2,"['OTSC2', 'otosclerosis 2']",,605727,,C1854022,,,,C565302,,,,
mondo:0011587,cataract 25,"['cataract 25', 'cataract, central pouch-like, with sutural opacities', 'cataract, central saccular, with sutural opacities', 'CTRCT25', 'cataract type 25', 'central saccular cataract with sutural opacities', 'central pouch-like cataract with sutural opacities', 'CCSSO']",0110254,605728,,,,,,C565301,,,,
mondo:0011588,platelet-type bleeding disorder 12,"['prostaglandin-endoperoxide synthase 1 deficiency, platelet', 'platelet cyclooxygenase 1 deficiency', 'BDPLT12', 'platelet COX1 deficiency', 'PGHS1 deficiency', 'bleeding disorder, platelet-type, 12', 'platelet prostaglandin-endoperoxide synthase 1 deficiency']",0111058,605735,,C2751535,,,,C567786,,,,
mondo:0011589,microphthalmia with coloboma 2,"['microphthalmia, colobomatous, isolated 2', 'MCOPCB2', 'microphthalmia, isolated, with coloboma 2']",,605738,,C1854018,,,,C565300,,,,
mondo:0011590,anisomastia,['anisomastia'],,605746,,,,,,C565299,,,,
mondo:0011591,cataract 26 multiple types,"['cataract 26, multiple types', 'cataract, autosomal recessive, early-onset, pulverulent', 'CTRCT26']",0110246,605749,98984,C1854003,,,,C565298,,,,
mondo:0011592,exudative vitreoretinopathy 3,"['exudative vitreoretinopathy 3', 'EVR3']",0111409,605750,,C1854002,,,,C565297,,,,
mondo:0011593,"seizures, benign familial infantile, 2","['convulsions, benign familial infantile, 2', 'seizures, benign familial infantile, 2', 'BFIS2', 'seizures, benign familial infantile, type 2']",0081115,605751,,C1853995,,,,C565296,,,,
mondo:0011594,"ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis","['gonadal dysgenesis, hypergonadotropic, 20 type, with short stature and recurrent metabolic acidosis', 'ovarian dysgenesis, hypergonadotropic, with short stature and recurrent metabolic acidosis']",,605756,,C3148970,,,,,,,,
mondo:0011595,nonsyndromic congenital nail disorder 7,"['Iso-Kikuchi syndrome', 'COIF syndrome', 'congenital isolated nail dysplasia', 'COIF', 'nonsyndromic congenital nail disorder type 7', 'isolated congenital nail dysplasia', 'nail disorder, nonsyndromic congenital, 7', 'congenital onychodysplasia of the index fingers', 'isolated congenital onychodysplasia', 'NDNC7', 'nail dysplasia, isolated congenital', 'onychodysplasia, isolated congenital']",0080085,605779,79144,C1853984,,,,C538333,,,,
mondo:0011596,"dermatitis, atopic, 2","['atopic dermatitis type 2', 'ATOD2', 'FLG atopic eczema', 'atopic eczema caused by mutation in FLG', 'dermatitis, ATOPIC, 2', 'dermatitis, Atopic, type 2', 'atopic dermatitis 2', 'dermatitis, atopic, susceptibility to, 2']",0110098,605803,,C1853965,,,,C565293,,,,
mondo:0011597,"dermatitis, atopic, 3","['atopic dermatitis with asthma', 'ATOD3', 'dermatitis, atopic, susceptibility to, 3', 'dermatitis, ATOPIC, 3', 'dermatitis, Atopic, with asthma', 'atopic dermatitis type 3']",0110099,605804,,C1853964,,,,C565292,,,,
mondo:0011598,"dermatitis, atopic, 4","['dermatitis, atopic, susceptibility to, 4', 'dermatitis, ATOPIC, 4', 'atopic dermatitis type 4', 'ATOD4']",0110100,605805,,C1853963,,,,C565291,,,,
mondo:0011599,birdshot chorioretinopathy,"['BSCR', 'multiple small, cream-colored lesions, symmetrically scattered mainly around the optic disk', 'multiple small, cream-colored lesions, symmetrically scattered mainly around the optic disc', 'vitiliginous choroiditis', 'birdshot retinochoroiditis', 'birdshot chorioretinitis', 'Bscr', 'birdshot chorioretinopathy', 'birdshot retinochoroidopathy']",0111079,605808,179,C1853959,,,,C537630,,,,
mondo:0011600,congenital myasthenic syndrome 4A,"['congenital myasthenic syndrome type Ia1', 'Cms Ia1', 'Cms Ia1, formerly', 'congenital myasthenic syndrome 4A slow-channel', 'congenital myasthenic syndrome type 4A', 'CMS Ia1', 'congenital myasthenic syndrometype Ia1', 'congenital myasthenic syndrome type Ia1, formerly', 'CMS4A', 'myasthenic syndrome, congenital, 4A, slow-channel', 'CMS1A1']",0110678,605809,,C1853949,,,,,,,,
mondo:0011601,neonatal intrahepatic cholestasis due to citrin deficiency,"['neonatal intrahepatic cholestasis caused by citrin deficiency', 'neonatal-onset citrullinemia type 2', 'citrullinemia, type II, neonatal-onset', 'citrullinemia, type II, neonatal-onset, with or without failure to thrive and dyslipidemia', 'cholestasis, neonatal intrahepatic, caused by citrin deficiency', 'NICCD', 'neonatal-onset citrullinemia type II', 'citrullinemia, type II, neonatal-onset, with or without failure to thrive and dyslipidaemia']",0070341,605814,247598,C4274030,"['-0.2407', '0.2595', '-0.02437', '0.1755', '0.1315', '-0.63', '-0.05804', '0.1521', '0.1776', '0.0742', '-0.05716', '-0.2468', '-0.03967', '0.3342', '-0.493', '-0.1869', '0.023', '0.372', '0.002539', '-0.787', '0.3691', '-0.3992', '0.5845', '0.1115', '-0.006874', '-0.10016', '0.3086', '0.0993', '-0.1572', '-0.3552', '0.373', '0.2477', '0.675', '0.8804', '-0.75', '-0.5205', '-0.515', '0.3335', '-0.6387', '-8.386e-05', '-0.1261', '-0.722', '0.274', '0.2164', '-0.2585', '-0.3308', '0.1796', '-0.069', '0.4211', '0.631', '-0.0118', '-0.11194', '-0.0985', '-0.4219', '-0.07324', '0.04523', '0.1453', '-0.1965', '-0.1669', '0.001417', '0.0407', '0.1361', '0.44', '-0.2983', '-0.3774', '0.076', '0.1409', '0.4177', '-0.554', '0.2708', '0.1998', '0.1483', '0.07086', '-0.1747', '0.09906', '0.03607', '0.626', '-0.006298', '-0.4036', '-0.0887', '-0.1484', '-0.01617', '-0.623', '-0.1791', '0.38', '0.4866', '0.1808', '0.01993', '0.7256', '-0.5117', '0.5645', '0.6147', '0.1061', '-0.2094', '0.332', '0.7285', '0.0952', '0.03622', '0.3733', '-0.03232']",,,C536398,,,,
mondo:0011602,autosomal recessive nonsyndromic hearing loss 27,"['DFNB27', 'autosomal recessive deafness 27', 'deafness, autosomal recessive 27', 'autosomal recessive nonsyndromic deafness type 27', 'autosomal recessive nonsyndromic deafness 27']",0110485,605818,,C1853941,,,,C565287,,,,
mondo:0011603,GNE myopathy,"['QSM', 'rimmed vacuole myopathy', 'inclusion body myopathy, autosomal recessive', 'NM', 'inclusion body myopathy autosomal recessive', 'inclusion body myopathy type 2', 'inclusion body myopathy, hereditary, autosomal recessive', 'inclusion body myopathy, quadriceps-sparing', 'myopathy, distal, with or without rimmed vacuoles', 'quadriceps-sparing myopathy', 'Nonaka myopathy', 'inclusion body myopathy 2, autosomal recessive', 'inclusion body myopathy 2, autosomal recessive, formerly', 'distal myopathy, Nonaka type', 'DMRV', 'Nonaka distal myopathy', 'hereditary inclusion body myopathy type 2', 'quadriceps sparing myopathy', 'IBM2', 'myopathy, distal, with rimmed vacuoles', 'HIBM2', 'distal myopathy with rimmed vacuoles']",0080718,605820,602,,"['-0.4697', '-0.01738', '-0.3716', '0.2344', '0.1676', '-0.682', '-0.0859', '0.7173', '-0.726', '-0.4983', '-0.612', '0.1952', '0.3228', '0.6343', '0.1897', '0.1986', '-0.1459', '-0.2456', '-0.1765', '-0.6724', '-0.0459', '-0.5146', '0.387', '0.2134', '-0.06354', '-0.004585', '-0.1357', '-0.0353', '-0.3354', '-0.3354', '0.901', '0.0874', '-0.553', '0.08344', '-0.136', '-0.1355', '-0.4338', '0.0988', '0.2769', '-0.1971', '-0.2217', '-1.034', '0.1686', '0.7686', '0.2135', '-0.0737', '-0.1328', '0.1686', '-0.4773', '0.1333', '0.006542', '0.0612', '-0.00741', '-0.8076', '-0.1774', '-0.956', '0.6885', '-0.472', '0.11414', '-0.509', '0.2693', '-0.1902', '0.2346', '-0.0892', '-0.3486', '0.2484', '0.556', '0.1682', '-0.00793', '0.0713', '-0.002962', '-0.509', '-0.1576', '0.7285', '0.3901', '0.407', '-0.6416', '-0.102', '-0.10614', '-0.3557', '0.4805', '-0.126', '0.8643', '0.4563', '-0.548', '0.3823', '-0.408', '0.175', '0.6514', '-0.1145', '0.282', '0.0477', '0.3547', '-0.004055', '0.535', '-0.138', '0.0094', '-0.391', '-0.4675', '-0.0735']",,,,,,,
mondo:0011604,spondylo-ocular syndrome,"['spondyloocular syndrome', 'SOS']",,605822,85194,,"['-0.1571', '0.04065', '0.1691', '-0.3525', '0.0564', '-0.2324', '-0.00966', '0.4841', '-0.3232', '-0.03534', '-0.09216', '-0.2045', '0.0491', '-0.0743', '-0.1141', '0.108', '0.407', '-0.07495', '-0.0739', '-0.2754', '-0.1176', '0.09155', '0.1299', '-0.2332', '0.03696', '0.08954', '-0.0769', '-0.0503', '0.1197', '0.03696', '0.2754', '-0.1366', '0.2089', '0.0934', '-0.04156', '-0.01356', '-0.04724', '-0.256', '-0.08685', '-0.387', '0.2554', '-0.2573', '0.0864', '-0.11005', '0.02705', '-0.0898', '0.03442', '0.3203', '-0.0632', '-0.1317', '0.0273', '0.0759', '0.1842', '0.06915', '-0.269', '-0.3782', '0.05655', '0.002636', '-0.04596', '-0.08234', '0.2008', '-0.1523', '-0.348', '0.07', '-0.1592', '0.0645', '0.2383', '0.4521', '-0.2103', '0.4048', '-0.2573', '0.1669', '0.089', '-0.07245', '-0.1428', '0.1335', '-0.05643', '-0.06305', '0.00692', '-0.1104', '-0.04846', '0.1067', '-0.1302', '0.591', '-0.26', '0.05646', '0.0315', '0.387', '0.3337', '0.07904', '0.0671', '0.2532', '0.0575', '0.1484', '0.5483', '-0.0651', '0.3396', '-0.0818', '0.2668', '0.10736']",,,,,,,
mondo:0011605,generalized basaloid follicular hamartoma syndrome,"['GBFHS', 'basaloid follicular hamartoma syndrome, generalized, autosomal dominant']",,605827,168632,C1853919,,,,C565284,,,,
mondo:0011606,baby rattle pelvis dysplasia,"['baby rattle pelvic dysplasia', 'baby rattle pelvis dysplasia']",,605838,,C1853911,,,,C565282,,,,
mondo:0011607,"narcolepsy 2, susceptibility to","['NRCLP2', 'narcolepsy 2', 'narcolepsy 2, susceptibility to']",,605841,,C1853901,,,,,,,,
mondo:0011608,"dermatitis, atopic, 5","['dermatitis, atopic, susceptibility to, 5', 'dermatitis, ATOPIC, 5', 'atopic dermatitis type 5', 'ATOD5']",0110101,605844,,C1853900,,,,C565280,,,,
mondo:0011609,"dermatitis, atopic, 6","['ATOD6', 'dermatitis, atopic, susceptibility to, 6', 'atopic dermatitis type 6', 'dermatitis, ATOPIC, 6']",0110102,605845,,C1853899,,,,C565279,,,,
mondo:0011610,dimethylglycine dehydrogenase deficiency,"['DMGDH deficiency', 'dimethylglycine dehydrogenase activity disease', 'disorder of dimethylglycine dehydrogenase activity', 'dimethylglycine dehydrogenase deficiency', 'DMGDHD', 'DMG dehydrogenase deficiency', 'Dmgdh deficiency']",,605850,243343,C1853892,"['-0.549', '0.072', '0.00499', '-0.023', '0.1656', '-0.4202', '-0.3877', '0.1537', '0.2336', '-0.3652', '-0.10736', '0.237', '-0.07416', '-0.3005', '0.0789', '0.335', '-0.00591', '-0.01089', '-0.2269', '-0.788', '-0.11523', '-0.311', '0.2515', '-0.2778', '-0.1958', '0.002203', '0.0826', '-0.0787', '-0.03099', '-0.5444', '0.0655', '0.1907', '0.2903', '0.1126', '-0.557', '-0.188', '-0.1317', '-0.1917', '0.06195', '-0.0994', '-0.04706', '-0.625', '-0.004093', '-0.4329', '-0.1051', '-0.1904', '-0.03253', '-0.03622', '-0.04672', '0.3452', '-0.2097', '-0.2615', '-0.03616', '0.1605', '-0.0323', '-0.6226', '0.3088', '-0.007664', '-0.479', '0.02382', '0.0902', '-0.1318', '0.2073', '-0.507', '-0.1566', '-0.143', '0.3743', '0.1777', '-0.562', '0.04105', '-0.3115', '-0.1393', '-0.1752', '0.0735', '0.219', '0.5347', '0.03418', '0.0856', '-0.003263', '0.09717', '0.3914', '0.0772', '0.2213', '0.3062', '0.598', '0.2783', '0.0831', '0.2072', '0.4958', '0.01851', '0.2017', '0.5244', '-0.04202', '-0.0811', '0.8247', '0.4634', '0.348', '-0.2369', '0.04504', '0.011986']",,,C565278,,,,
mondo:0011611,"short stature, intellectual disability, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting","['short stature, intellectual disability, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting', 'short stature, mental retardation, callosal agenesis, Heminasal hypoplasia, microphthalmia, and atypical clefting']",,605856,,C1970039,,,,C566989,,,,
mondo:0011612,glycine encephalopathy,"['Glycine synthase deficiency', 'nonketotic hyperglycinemia', 'hyperglycinemia, transient neonatal', 'GCE', 'hyperglycinemia, Nonketotic', 'glycine encephalopathy', 'non-ketotic hyperglycinemia', 'GLYCINE encephalopathy', 'hyperglycinemia nonketotic', 'NKA']",9268,605899,407,C0751748,"['0.3381', '0.3591', '-0.4011', '-0.003788', '-0.11487', '-0.5444', '-0.2142', '0.1631', '-0.8594', '-0.2389', '-0.3643', '-0.5054', '0.518', '0.382', '0.1077', '-0.05112', '-0.3462', '-0.9434', '-0.1349', '-0.3164', '0.638', '-0.05444', '0.4514', '-0.046', '0.07135', '-0.4656', '0.4717', '0.00464', '-0.4397', '0.2323', '0.4849', '0.2544', '0.3408', '0.4785', '-0.464', '0.3584', '-0.6997', '-0.4182', '0.2229', '-0.03702', '0.07623', '-0.8335', '0.569', '-0.2698', '0.2056', '-0.212', '-0.000607', '-0.2292', '-0.5894', '0.8623', '-0.4878', '-0.04538', '-0.3936', '-0.5767', '-0.1528', '0.2632', '-0.00873', '0.2179', '-0.2932', '0.5728', '0.10846', '-0.04913', '0.7173', '-0.006737', '-0.1503', '0.5127', '0.529', '0.05127', '-0.8716', '0.2925', '-0.1306', '-0.1335', '-0.3079', '0.4563', '0.3486', '0.2563', '0.297', '-0.1952', '-0.2983', '0.4104', '-0.08826', '0.2296', '-0.4329', '0.0995', '0.393', '0.5703', '0.04907', '0.0532', '0.2399', '0.1703', '0.3794', '0.2559', '-0.1145', '0.5327', '0.1194', '0.552', '0.3186', '-0.2483', '0.4988', '-0.00543']",C84937,,,270.7,,,
mondo:0011613,autosomal recessive early-onset Parkinson disease 6,"['Parkinson disease 6, late-onset, susceptibility to', 'early-onset Parkinson disease 6', 'autosomal recessive early-onset Parkinson^s disease 6', 'PINK1 Parkinson disease', 'Parkinson disease 6, autosomal recessive early-onset', 'Parkinson disease, autosomal recessive early-onset, digenic, Pink1/Dj1', 'autosomal recessive early-onset Parkinson disease type 6', 'Parkinson disease 6, early-onset', 'Parkinson disease 6, early onset', 'PARK6', 'Parkinson disease caused by mutation in PINK1']",0060369,605909,,,,,,C565276,,,,
mondo:0011614,3-hydroxy-3-methylglutaryl-CoA synthase deficiency,"['HMG CoA synthetase deficiency', 'HMG-CoA synthase-2 deficiency', 'HMGCS2D', 'HMG-CoA synthase deficiency', 'mitochondrial HMG-Coa synthase deficiency', '3-hydroxy-3-methylglutaryl-CoA synthase-2 deficiency', 'Hmgcs2 deficiency']",0081168,605911,35701,C2751532,"['0.1956', '0.3403', '-0.435', '0.00794', '0.2056', '-0.0968', '-0.084', '-0.2292', '0.1637', '0.0678', '-0.04102', '-0.2703', '0.2402', '0.2242', '-0.3777', '-0.3403', '-0.2289', '-0.1396', '-0.4734', '-0.8433', '-0.3364', '-0.296', '0.2554', '-0.7896', '-0.3755', '-0.2705', '-0.397', '0.1268', '-0.2062', '-0.0632', '0.1747', '0.719', '0.289', '0.5347', '-0.8354', '-0.163', '0.369', '-0.0272', '-0.2988', '-0.03503', '-0.2062', '-0.6396', '0.445', '-0.05734', '-0.10803', '0.004223', '-0.2825', '-0.1929', '0.2367', '0.622', '0.2332', '0.02242', '0.1109', '0.05496', '0.01959', '-0.239', '0.6904', '-0.215', '-0.276', '0.263', '0.5337', '0.5312', '0.55', '-0.56', '-0.1921', '0.10767', '0.2798', '0.3413', '-0.965', '0.03955', '-0.4128', '0.488', '-0.04004', '-0.2717', '0.2896', '0.76', '-0.2107', '-0.1565', '-0.3008', '-0.0709', '0.5386', '-0.2576', '-0.02498', '-0.1343', '0.579', '0.5386', '-0.1401', '-0.0993', '0.713', '-0.5684', '0.6816', '0.5005', '-0.584', '0.3044', '0.4353', '1.104', '0.4646', '-0.1459', '0.04535', '0.31']",,,C567784,,,,
mondo:0011615,East Texas bleeding disorder,"['Bdet', 'bleeding disorder, EAST Texas type']",,605913,391320,C1853831,,,,C565275,,,,
mondo:0011616,holoprosencephaly 6,"['HPE6', 'holoprosencephaly type 6', 'holoprosencephaly 6']",0110874,605934,,C1853830,,,,C565274,,,,
mondo:0011617,"arthropathy, erosive","['arthropathy, erosive']",,605935,,C1853829,,,,C565273,,,,
mondo:0011618,liver fibrocystic disease and polydactyly,['liver fibrocystic disease and polydactyly'],,605944,,C1853827,,,,C565272,,,,
mondo:0011619,crumpled helices and small mouth,"['crumpled helices and small mouth', 'sparse hair, prominent nose, small mouth, micrognathia, cleft palate, crumpled upper helices, digit anomaly, and mild developmental delay']",,605945,,C1853826,,,,C536217,,,,
mondo:0011620,"metaphyseal dysplasia, Braun-Tinschert type","['metaphyseal dysplasia, Braun-Tinschert type']",,605946,85188,C1853825,,,,C565271,,,,
mondo:0011621,acropectoral syndrome,"['ACRP syndrome', 'ACRPS', 'syndactyly-preaxial polydactyly-sternal deformity syndrome', 'acro-pectoral syndrome', 'syndactyly, preaxial polydactyly, and sternal deformity', 'syndactyly, preaxial polydactyly and sternal deformity', 'acropectoral syndrome', 'Dundar Acropectoral syndrome']",,605967,85203,C1853812,,,,C535664,,,,
mondo:0011622,"nephrolithiasis, uric acid, susceptibility to","['urolithiasis, uric acid, susceptibility to', 'susceptibility to uric acid nephrolithiasis', 'UAN', 'nephrolithiasis, uric acid, susceptibility to']",,605990,,,,,,,,,,
mondo:0011624,transaldolase deficiency,"['TALDO deficiency', 'transaldolase deficiency', 'Eyaid syndrome', 'Taldo deficiency']",,606003,101028,C1291329,"['-0.202', '0.4893', '-0.02876', '-0.0353', '0.25', '-0.2961', '-0.3638', '0.4868', '-0.1364', '-0.1028', '-0.2231', '-0.2479', '0.2213', '-0.1032', '-0.2286', '0.2249', '0.03302', '0.3013', '-0.3242', '-0.3022', '0.0609', '-0.1647', '0.4373', '-0.2178', '0.0965', '-0.1293', '-0.1085', '0.319', '0.6055', '-0.2712', '0.26', '-0.1545', '0.3103', '0.1763', '0.138', '-0.4448', '-0.2515', '-0.4844', '-0.2045', '0.1532', '-0.2673', '-0.3276', '-0.03952', '-0.192', '-0.2834', '-0.1901', '0.1233', '0.0857', '-0.4854', '-0.2703', '-0.1768', '-0.4036', '-0.2267', '0.3098', '-0.1855', '-0.352', '0.0474', '0.08704', '0.01049', '0.3008', '0.3784', '0.0356', '-0.00916', '0.1116', '0.2119', '-0.1985', '0.1721', '0.4766', '-0.1873', '0.01872', '-0.1351', '0.1522', '0.06824', '0.03903', '-0.07745', '0.3105', '0.2573', '-0.3784', '0.1539', '-0.1725', '0.3125', '0.08', '0.09906', '0.0952', '0.12115', '0.301', '0.255', '0.3438', '0.2976', '-0.00398', '0.4443', '0.256', '0.192', '-0.3582', '0.7905', '0.602', '0.387', '-0.467', '0.2737', '0.04144']",,,C563207,277.6,,,
mondo:0011625,autosomal dominant nonsyndromic hearing loss 18,"['deafness, autosomal dominant 18', 'autosomal dominant nonsyndromic deafness type 18', 'autosomal dominant deafness 18', 'DFNA18', 'autosomal dominant nonsyndromic deafness 18']",0110549,606012,,C1853760,,,,C565267,,,,
mondo:0011626,"acromegaloid features, overgrowth, cleft palate, and hernia","['acromegaloid features, overgrowth, cleft palate and hernia', 'Aoch', 'acromegaloid features, overgrowth, cleft palate, and hernia']",,606049,,C1853757,,,,C535656,,,,
mondo:0011627,"autism, susceptibility to, 5","['autism, susceptibility to, 5', 'autism-related speech delay', 'phrase speech delay, autism-related', 'intellectual developmental disorder with autism and speech delay', 'AUTS5']",,606053,,C1853755,,,,,,,,
mondo:0011628,propionic acidemia,"['GLYCINEMIA, ketotic', 'PCC deficiency', 'propionic aciduria', 'Glycinemia, ketotic', 'ketotic glycinemia', 'ketotic hyperglycinemia', 'propionic acidemia', 'prop', 'ketotic II glycinemia', 'propionyl-Coa carboxylase deficiency', 'propionyl-CoA carboxylase deficiency', 'Propionicacidemia', 'hyperglycinemia with ketoacidosis and leukopenia']",14701,606054,35,C0268579,"['0.01906', '0.526', '-0.52', '-0.4158', '-0.2155', '-0.7485', '-0.2896', '0.537', '-0.02217', '-0.2908', '-0.573', '-0.11285', '0.5586', '-0.1777', '-0.3218', '-0.2678', '-0.1372', '-0.4536', '-0.3083', '-0.9004', '0.03087', '-0.564', '0.09467', '-0.1989', '-0.02097', '-0.3223', '-0.0683', '0.1276', '-0.528', '-0.4917', '0.3108', '0.5244', '0.573', '0.274', '-0.3428', '-0.0271', '0.03069', '0.2203', '-0.3076', '0.4106', '-0.0541', '-0.4453', '0.7803', '-0.1123', '-0.02284', '0.271', '0.08026', '-0.1438', '0.594', '0.375', '-0.656', '-0.1271', '0.09283', '-0.4565', '0.3', '0.349', '0.611', '0.1342', '0.1135', '0.11664', '-0.184', '0.02966', '0.4968', '-0.2856', '-0.243', '0.2145', '0.4768', '0.1209', '-0.0929', '0.4534', '-0.703', '0.1055', '-0.1759', '-0.2251', '-0.1044', '0.3684', '0.2335', '0.0736', '-0.417', '0.1516', '0.3088', '-0.1971', '-0.403', '0.03876', '0.8804', '0.3179', '0.2742', '-0.528', '0.1324', '0.2092', '-0.03625', '0.519', '-0.1307', '0.2472', '-0.27', '0.637', '0.2335', '-0.3943', '-0.3745', '-0.0849']",C85030,,D056693,,E71.121,,
mondo:0011629,MOGS-congenital disorder of glycosylation,"['MOGS-CDG', 'CDG IIb', 'glucosidase 1 deficiency', 'carbohydrate deficient glycoprotein syndrome type IIb', 'congenital disorder of glycosylation, type IIb', 'congenital disorder of glycosylation type 2b', 'GCS1-CDG', 'CDG 2B', 'CDG syndrome type IIb', 'CDG-IIb', 'MOGS-CDG (CDG-IIb)', 'congenital disorder of glycosylation type IIb', 'CDG2B']",0070254,606056,79330,C1853736,"['0.083', '0.2612', '0.504', '-0.6724', '0.2222', '-0.5933', '0.202', '0.178', '-0.3516', '-0.533', '-0.03857', '-0.1284', '-0.02592', '-0.3633', '-0.597', '0.3298', '0.554', '-0.06027', '-0.4307', '-0.4062', '0.3206', '0.06836', '0.3428', '-0.11633', '0.04382', '0.10016', '-0.01105', '0.1216', '0.2727', '-0.5166', '0.3145', '0.4917', '0.641', '-0.0661', '0.06055', '0.2062', '-0.04105', '0.2832', '-0.568', '-0.514', '-0.10065', '-0.4077', '0.1409', '-0.03714', '-0.5474', '0.078', '0.0935', '0.403', '0.5605', '0.563', '-0.608', '0.02495', '0.2189', '0.07947', '-0.25', '-0.2175', '0.05597', '-0.293', '-0.1934', '0.2598', '0.1869', '0.303', '0.01507', '0.208', '0.1458', '-0.0635', '0.2189', '0.01587', '-0.3274', '0.4885', '-0.4778', '0.3552', '0.571', '0.3767', '-0.3345', '-0.2244', '0.8125', '-0.1897', '-0.1936', '0.4185', '-0.3657', '0.1266', '-0.1628', '0.2979', '-0.1382', '0.2732', '0.00446', '0.272', '0.3765', '0.3909', '-0.1985', '0.515', '-0.0372', '0.1002', '0.3677', '0.57', '0.708', '-0.1364', '0.06012', '0.1425']",,,C565264,,,,
mondo:0011630,retinitis pigmentosa 28,"['retinitis pigmentosa caused by mutation in FAM161A', 'retinitis pigmentosa type 28', 'retinitis pigmentosa 28', 'RP 28', 'RP28', 'FAM161A retinitis pigmentosa']",0110365,606068,,C1419614,,,,,,H35.5,,
mondo:0011631,hemochromatosis type 4,"['hemochromatosis due to defect in ferroportin', 'HFE4', 'ferroportin disease', 'autosomal dominant hereditary hemochromatosis', 'hemochromatosis, autosomal dominant', 'hereditary hemochromatosis caused by mutation in SLC40A1', 'hemochromatosis, type 4', 'SLC40A1 hereditary hemochromatosis']",0111028,606069,648562,C1853733,"['0.4268', '0.3716', '-0.4368', '0.0547', '0.7344', '-0.3054', '-0.7104', '0.5073', '0.305', '-0.0751', '-0.0745', '0.3013', '-0.592', '0.3984', '-0.4485', '0.03708', '-0.4358', '0.138', '-0.3035', '-0.9253', '-0.6235', '-0.2378', '0.4194', '-0.2783', '0.12213', '-0.1626', '0.10004', '-0.1831', '0.2744', '-0.011765', '0.9014', '-0.647', '0.8506', '0.06775', '-0.2181', '-0.5044', '-0.8027', '0.06537', '0.3157', '0.2079', '0.3882', '-0.0992', '-0.06744', '0.4058', '0.4177', '-1.079', '0.05936', '-0.5957', '0.09467', '-0.06635', '0.3726', '-0.1738', '0.4617', '0.2415', '0.2023', '-0.3418', '0.2627', '0.5596', '-0.199', '0.00977', '0.0961', '0.87', '0.388', '-0.1906', '-0.01248', '0.1707', '-0.2722', '0.2134', '-0.849', '-0.3806', '-0.0881', '0.1667', '0.648', '-0.308', '0.3608', '-0.3848', '-0.1946', '1.044', '-0.45', '0.7383', '-0.01152', '-0.2039', '-0.1912', '-0.4177', '-0.0559', '-0.6733', '1.0205', '0.264', '0.4885', '0.0582', '1.096', '0.4094', '-0.5083', '-0.1825', '0.585', '0.7163', '0.1295', '-0.625', '-0.1296', '0.1788']",,,C537249,,,,
mondo:0011632,amyotrophic lateral sclerosis type 21,"['amyotrophic lateral sclerosis 21', 'ALS21', 'myopathy, distal, 2', 'MATR3 amyotrophic lateral sclerosis', 'amyotrophic lateral sclerosis type 21', 'vocal cord and pharyngeal dysfunction with distal myopathy', 'vocal cord and pharyngeal dysfunction with distal myopathy, formerly', 'amyotrophic lateral sclerosis caused by mutation in MATR3', 'myopathy, distal, 2, formerly']",0060212,606070,600,,"['0.03412', '-0.633', '-0.2837', '-0.2566', '0.1387', '-0.5425', '0.2175', '0.5327', '-0.544', '-0.766', '-0.1987', '-0.02962', '-0.748', '0.2622', '0.2698', '-0.10516', '0.2223', '-0.798', '0.00663', '-0.836', '-0.2366', '-0.09235', '0.1361', '0.6396', '0.0679', '-0.3232', '0.1676', '-0.257', '-0.248', '-0.4285', '0.1168', '0.3462', '0.1294', '-0.4963', '0.02681', '-0.5854', '-0.501', '0.05447', '0.5396', '-0.614', '-0.369', '-0.5947', '-0.10645', '0.3186', '-0.1793', '0.2803', '-0.1356', '0.2605', '-0.5605', '0.242', '0.1113', '-0.2625', '0.623', '-0.5693', '-0.2079', '-0.4688', '0.5986', '0.1439', '0.265', '0.08466', '0.601', '-0.05707', '0.00827', '0.04453', '-0.6094', '-0.09344', '-0.01258', '0.2622', '-0.1147', '0.2559', '-0.3743', '-0.05545', '0.4163', '0.2776', '0.4912', '0.1066', '0.418', '-0.337', '-0.1978', '-0.244', '0.5605', '-0.3186', '0.9062', '0.3994', '-0.0714', '0.6646', '-0.3538', '-0.2576', '0.6475', '-0.658', '0.435', '-0.1043', '-0.6055', '0.6753', '0.473', '0.3315', '0.384', '-0.3105', '-0.3289', '-0.004738']",C168755,,,,,,
mondo:0011633,Charcot-Marie-Tooth disease axonal type 2C,"['Charcot-Marie-Tooth disease type 2C', 'HMSN2C', 'HMSN 2C', 'CMT 2C', 'HMSN 2 C', 'hereditary motor and sensory neuropathy 2 C', 'CMT2C', 'Charcot-Marie-Tooth neuropathy type 2C', 'autosomal cominant axonal Charcot-Marie-Tooth disease type 2C', 'hereditary motor and sensory neuropathy, type 2C', 'autosomal dominant Charcot-Marie-Tooth disease type 2C', 'Charcot-Marie-Tooth disease, axonal, type 2C', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2C', 'Charcot-Marie-Tooth disease type 2 caused by mutation in TRPV4', 'TRPV4 Charcot-Marie-Tooth disease type 2', 'Charcot Marie Tooth disease type 2C', 'hereditary motor and sensory neuropathy type IIc', 'hereditary motor and sensory neuropathy, type IIC', 'Charcot-Marie-Tooth neuropathy, type 2C']",0110182,606071,99937,,"['0.2986', '0.412', '0.307', '0.03044', '0.03745', '-0.4246', '0.2676', '0.715', '-0.578', '-0.1707', '-0.01118', '0.285', '-0.6343', '0.525', '-0.1816', '-0.1935', '-0.2544', '-0.44', '-0.586', '-0.6987', '0.0649', '0.4214', '0.195', '0.9023', '0.3623', '0.281', '0.1743', '0.3452', '0.204', '-0.3286', '0.1412', '-0.656', '0.03717', '-0.01723', '0.4956', '-0.7407', '-0.603', '-0.292', '0.3484', '-0.03354', '-1.66', '-0.2666', '0.1007', '0.1583', '-0.4358', '-0.3513', '0.3284', '-0.2443', '-0.4011', '0.1368', '0.2896', '0.4841', '-0.2705', '-1.275', '0.2494', '-0.2827', '-0.1996', '0.3782', '-0.592', '-0.1829', '-0.4236', '-0.09534', '0.605', '0.9307', '-0.505', '0.964', '-0.1771', '0.663', '-0.4177', '0.3662', '-0.757', '0.0647', '0.624', '-0.3564', '1.028', '0.581', '-0.1577', '0.644', '0.088', '-0.1483', '-0.133', '-0.0799', '0.902', '0.883', '0.1185', '-0.2559', '0.394', '0.53', '0.5264', '0.4321', '0.3123', '-0.008156', '0.3357', '0.3494', '0.4614', '0.4905', '0.6265', '-0.73', '0.006065', '0.8325']",,,,,,,
mondo:0011634,rippling muscle disease,,,,,,,,,,359.29,,10069417,
mondo:0011635,"goiter, multinodular 3","['MNG3', 'goiter, multinodular, 3', 'goiter, multinodular 3']",,606082,,C1853686,,,,C565260,,,,
mondo:0011636,Diamond-Blackfan anemia 2,"['anaemia Diamond-Blackfan 2', 'anemia Diamond-Blackfan 2', 'Diamond-Blackfan anemia 2', 'Diamond-Blackfan Anemia, 2', 'DBA2']",0111885,606129,,C1853666,,,,C536130,,,,
mondo:0011637,Sener syndrome,"['polycystic brain (cerebrum polycystica vera) associated with ectodermal dysplasia', 'frontonasal dysplasia and dilated Virchow-Robin spaces', 'Sener syndrome']",,606156,,C1853616,,,,C537579,,,,
mondo:0011638,neuroferritinopathy,"['neurodegeneration with brain iron accumulation 3', 'NBIA3', 'ferritin-related neurodegeneration', 'neurodegeneration with brain iron accumulation type 3', 'basal ganglia disease adult-onset', 'hereditary ferritinopathy', 'basal ganglia disease, adult-onset', 'neuroferritinopathy', 'adult basal ganglia disease', 'Neuroferritinopathy; basal ganglia disease, adult-onset']",0110737,606159,157846,C1853578,"['0.0817', '0.4604', '-0.1304', '-0.5527', '-0.347', '-0.2727', '0.3333', '0.3538', '-0.8354', '-0.366', '-0.1533', '0.03348', '-0.3171', '0.08875', '0.6484', '-0.2542', '-0.1162', '-0.6104', '-0.4504', '-0.4983', '-0.34', '-0.578', '0.12427', '0.1901', '-0.08325', '0.0858', '-0.1897', '-0.6997', '-0.6333', '0.3079', '0.2544', '-0.03696', '0.2332', '-0.08234', '0.3965', '-0.2715', '-0.3286', '-0.605', '-0.2615', '0.2668', '0.431', '-0.496', '0.2742', '0.4824', '0.7363', '-0.3848', '-0.0508', '0.3', '0.0436', '0.1764', '-0.04895', '0.4036', '0.1492', '-0.2119', '-0.0916', '-0.2242', '0.2554', '-0.1003', '-0.05212', '0.1658', '0.2317', '-0.003214', '0.0084', '-0.8057', '-0.8745', '-0.02861', '0.706', '-0.08575', '0.2913', '0.1422', '0.19', '-0.4302', '0.005623', '0.1361', '0.1716', '0.7417', '-0.2646', '-0.11145', '-0.3533', '-0.3816', '0.2563', '-0.81', '0.295', '0.4927', '0.5586', '0.3167', '0.1175', '-0.001926', '1.045', '0.2151', '0.3474', '0.321', '-0.1123', '0.09796', '0.2438', '0.373', '0.2776', '0.11145', '0.4607', '0.315']",,,C548080,333.0,,,
mondo:0011639,Diamond-Blackfan anemia 15 with mandibulofacial dysostosis,"['Diamond-Blackfan anemia caused by mutation in RPS28', 'Diamond Blackfan anemia 15 with mandibulofacial dysostosis', 'DBA15', 'Diamond-Blackfan anemia 15 with mandibulofacial dysostosis', 'Diamond Blackfan anaemia 15 with mandibulofacial dysostosis', 'Diamond-Blackfan anaemia caused by mutation in RPS28', 'RPS28 Diamond-Blackfan anaemia', 'RPS28 Diamond-Blackfan anemia']",0111894,606164,,C4225411,,,,,,,,
mondo:0011640,genitopatellar syndrome,"['GTPTS', 'genitopatellar syndrome', 'absent patellae, scrotal hypoplasia, renal anomalies, Facial Dysmorphism, and mental retardation', 'absent patellae-scrotal hypoplasia-renal anomalies-facial dysmorphism-intellectual disability syndrome', 'GENITOPATELLAR syndrome', 'absent patellae, scrotal hypoplasia, renal anomalies, Facial Dysmorphism, and intellectual disability']",,606170,85201,C1853566,"['-0.2942', '0.1865', '0.3801', '-0.3813', '0.1409', '-0.2532', '-0.03062', '0.4617', '-0.533', '-0.1409', '-0.0439', '0.1048', '0.206', '-0.268', '-0.327', '0.00613', '0.3604', '-0.03592', '-0.0642', '-0.3772', '0.04663', '0.002253', '0.2068', '-0.03046', '0.1315', '0.00966', '-0.1603', '-0.03134', '0.416', '-0.3652', '0.2129', '-0.113', '0.3076', '0.4028', '0.3188', '-0.1721', '-0.05783', '-0.06946', '-0.0984', '-0.538', '0.10626', '-0.07916', '-0.09973', '-0.1035', '-0.02611', '-0.1758', '0.1855', '0.569', '-0.0754', '0.007008', '-0.4634', '-0.04303', '-0.1276', '0.0732', '-0.4185', '-0.3208', '-0.08057', '-0.11304', '-0.2238', '0.0448', '0.0792', '0.2477', '-0.398', '0.2164', '0.09534', '-0.09344', '0.2676', '0.1825', '-0.29', '0.2905', '-0.332', '0.1721', '0.2198', '-0.1086', '-0.222', '0.0429', '0.162', '-0.36', '-0.2786', '-0.06946', '0.05444', '-0.0246', '-0.0684', '0.501', '-0.02571', '-0.0329', '-0.2285', '0.5117', '0.0919', '0.0963', '0.002449', '0.368', '0.3591', '0.065', '0.4336', '-0.0569', '0.2888', '-0.4158', '0.2496', '0.269']",,,C565255,759.89,,,
mondo:0011641,"baculum, congenital absence of","['baculum, congenital absence of', 'Os penis, congenital absence of']",,606174,,,,,,,,,,
mondo:0011642,carnitine acetyltransferase deficiency,"['Acetyl-carnitine deficiency', 'CrAT', 'carnitine acetyltransferase deficiency', 'acetyl-carnitine deficiency']",,606175,,CN035113,,,,C563249,277.6,,,
mondo:0011644,pars planitis,"['familial pars planitis (subtype)', 'pars plana of ciliary body inflammation', 'pars planitis', 'pars plana of ciliary bodyitis', 'posterior cyclitis', 'peripheral retinal inflammation']",12731,606177,,C0030593,,C34903,1001088,D015868,363.21,,10034052,
mondo:0011646,laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy,['laryngeal abductor paralysis with cerebellar ataxia and motor neuropathy'],,606183,,C1853556,,,,C565252,,,,
mondo:0011647,Alzheimer disease 7,"['Alzheimer^s disease 7', 'Alzheimer disease type 7', 'AD7', 'Alzheimer disease 7', 'Alzheimer disease-7', 'Alzheimer disease, familial 7', 'Alzheimer^s disease type 7', 'Ad7', 'Alzheimer disease, familial, 7']",0110039,606187,,C1853555,,,,C565251,,,,
mondo:0011648,radiation-induced meningioma,"['Mnri', 'meningioma, radiation-induced', 'radiation induced meningioma']",,606190,,C1853554,,,,C536266,,,,
mondo:0011650,"atrioventricular septal defect, susceptibility to, 2","['atrioventricular septal defect, susceptibility to, type 2', 'CRELD1 atrioventricular septal defect', 'AVSD2', 'atrioventricular septal defect, susceptibility to, 2', 'atrioventricular septal defect, partial, with heterotaxy syndrome', 'atrioventricular septal defect caused by mutation in CRELD1', 'susceptibility to atrioventricular septal defect 2']",,606217,,,,,,C565249,,,,
mondo:0011651,"intellectual disability, short stature, facial anomalies, and joint dislocations","['intellectual disability, short stature, facial anomalies, and JOINT dislocations', 'intellectual developmental disorder with short stature, facial anomalies, and speech defects', 'mental retardation, short stature, facial anomalies, and JOINT dislocations']",,606220,,C1853507,,,,C565248,,,,
mondo:0011652,Phelan-McDermid syndrome,"['telomeric 22Q13 monosomy syndrome', 'PHMDS', 'Phelan-McDermid syndrome', '22q13 deletion', 'chromosome 22Q13.3 deletion syndrome', 'PHELAN-McDermid syndrome', 'monosomy type 22q13', 'deletion 22q13.3 syndrome', '22q13.3 deletion syndrome', 'Phelan McDermid syndrome']",0080354,606232,48652,C1853490,"['-0.2114', '0.1439', '0.3318', '-0.4888', '0.1225', '0.0339', '-0.1742', '0.7676', '-0.4094', '-0.3357', '-0.1641', '0.3003', '0.78', '-0.1289', '0.6006', '0.526', '0.284', '-0.292', '-0.4385', '-0.672', '0.1525', '0.1188', '0.2969', '-0.3774', '0.2817', '-0.3232', '-0.2424', '0.3445', '0.414', '-0.4321', '0.6445', '-0.1505', '0.6265', '0.1014', '-0.129', '-0.4287', '0.06537', '-0.2715', '0.05936', '-0.522', '0.1422', '0.10547', '0.2426', '-0.02293', '0.4158', '-0.824', '-0.06494', '0.1964', '0.13', '-0.07745', '-0.667', '-0.10767', '-0.751', '-0.1547', '-0.2301', '-0.0796', '0.2961', '0.2102', '0.06235', '0.0683', '0.06274', '0.3064', '-0.1136', '0.4905', '0.4841', '0.1501', '-0.1107', '0.0802', '0.1381', '0.4148', '-0.5107', '0.278', '-0.425', '0.0642', '0.1573', '0.2368', '0.4236', '0.1385', '-0.503', '-0.04172', '0.4375', '0.08453', '0.3535', '0.4858', '-0.1499', '0.55', '-0.1077', '-0.0968', '0.416', '0.3728', '0.07', '0.583', '-0.549', '0.257', '0.172', '-0.04285', '-0.1113', '-0.3232', '0.4045', '0.2368']",C157124,,C536801,758.39,,,
mondo:0011653,"thyroid cancer, nonmedullary, 3","['NMTC3', 'thyroid cancer, nonmedullary, 1, formerly', 'thyroid cancer, nonmedullary, 3', 'thyroid cancer, nonmedullary, 1', 'thyroid carcinoma, nonmedullary, 3']",,606240,,C1853488,,,,,,,,
mondo:0011654,"intellectual disability, microcephaly, growth retardation, joint contractures, and facial dysmorphism","['Kondoh syndrome', 'mental retardation, microcephaly, growth retardation, JOINT contractures, and facial dysmorphism', 'intellectual disability, microcephaly, growth retardation, JOINT contractures, and facial dysmorphism']",,606242,,C1853480,,,,C565246,,,,
mondo:0011655,alveolar soft part sarcoma,"['alveolar soft Part sarcoma', 'adult alveolar soft Part sarcoma', 'alveolar soft-tissue sarcoma', 'alveolar soft part sarcoma (disease)', 'ASPS', 'alveolar soft part sarcoma', 'alveolar soft tissue sarcoma', 'paediatric alveolar soft Part sarcoma', 'alveolar soft-part sarcoma', 'adult alveolar soft part sarcoma', 'alveolar soft PART sarcoma', 'pediatric alveolar soft Part sarcoma', 'adult alveolar soft-Part sarcoma', 'childhood alveolar soft part sarcoma']",4239,606243,163699,C0279544,,C7943,0007143,D018234,171.9,,10001882,0012218
mondo:0011656,paget disease of bone 4,"['PDB4', 'Paget disease of bone 4']",0081367,606263,,C1853473,,,,C565240,,,,
mondo:0011657,autosomal dominant nonsyndromic hearing loss 24,"['autosomal dominant nonsyndromic deafness type 24', 'autosomal dominant deafness 24', 'DFNA 24', 'DFNA24', 'deafness, autosomal dominant 24', 'deafness, autosomal dominant nonsyndromic sensorineural 24', 'autosomal dominant nonsyndromic deafness 24']",0110554,606282,,C1853451,,,,C565239,,,,
mondo:0011658,autosomal recessive early-onset Parkinson disease 7,"['PARK7', 'autosomal recessive early-onset Parkinson^s disease 7', 'Parkinson disease caused by mutation in PARK7', 'PARK7 Parkinson disease', 'autosomal recessive early-onset Parkinson disease type 7', 'Parkinson disease 7, autosomal recessive early-onset']",0060370,606324,,C1853445,,,,C565238,,,,
mondo:0011659,"heterotaxy, visceral, 3, autosomal","['HTX3', 'heterotaxy, visceral, 3, autosomal']",,606325,,C1853444,,,,C565237,,,,
mondo:0011660,autosomal dominant nonsyndromic hearing loss 22,"['deafness, autosomal dominant 22, with hypertrophic cardiomyopathy', 'DFNA22', 'autosomal dominant nonsyndromic deafness caused by mutation in MYO6', 'autosomal dominant nonsyndromic deafness type 22', 'MYO6 autosomal dominant nonsyndromic deafness', 'deafness, autosomal dominant nonsyndromic sensorineural 22', 'deafness, autosomal dominant 22', 'autosomal dominant deafness 22', 'deafness, autosomal dominant type 22', 'autosomal dominant nonsyndromic deafness 22', 'DFNA 22']",0110552,606346,228012,,"['0.1896', '-0.3518', '-0.2347', '0.725', '-0.0387', '0.06995', '0.2783', '1.567', '-0.02501', '-0.2646', '0.46', '-0.261', '-0.385', '0.4578', '-0.4856', '-0.7246', '-0.782', '-0.643', '-0.8105', '-0.7446', '0.3599', '0.0304', '-0.0629', '0.474', '0.1027', '-0.2893', '-0.278', '0.2837', '0.5347', '0.2482', '0.8916', '-0.06476', '0.2246', '0.2201', '-0.2744', '-0.1294', '0.01709', '0.0905', '0.3562', '-0.4646', '0.6177', '0.07654', '0.4292', '-0.01048', '0.0871', '0.2177', '-0.9165', '0.3354', '-0.08435', '-0.2267', '0.2067', '-0.09784', '-0.05865', '0.398', '0.3408', '-0.694', '-0.4856', '0.894', '0.01097', '-0.4072', '-0.2313', '0.3486', '0.122', '-0.4136', '-0.533', '0.1398', '0.1887', '0.5156', '-0.5366', '0.5654', '-0.1768', '0.5396', '0.8037', '-0.6196', '-0.2927', '0.1575', '-0.0977', '-0.1069', '0.06082', '0.586', '0.891', '-0.4146', '-0.02365', '-0.1813', '0.5703', '-0.2854', '0.6357', '0.1802', '0.4553', '0.6577', '0.1476', '-0.4763', '-0.6865', '0.2102', '0.765', '0.638', '0.307', '-0.358', '-0.6895', '0.3442']",,,C538197,,,,
mondo:0011661,inflammatory bowel disease 5,"['inflammatory bowel disease type 5', 'IBD5', 'inflammatory bowel disease 5']",0110889,606348,,C1853438,,,,C565234,,,,
mondo:0011662,pathological gambling,"['compulsive gambling', 'gambling, pathologic', 'pathological gambling']",12399,606349,,,,C94335,1001926,D005715,312.31,F63.0,,
mondo:0011663,juvenile primary lateral sclerosis,"['Pls, juvenile', 'juvenile PLS', 'PLSJ', 'primary lateral sclerosis, juvenile', 'PLS juvenile', 'JPLS']",,606353,247604,C1853396,"['-0.3228', '0.3066', '-0.03183', '-0.1169', '-0.448', '-0.4878', '0.0907', '1.173', '-1.121', '-0.4277', '-0.03284', '0.06018', '-0.2178', '-0.258', '1.266', '-0.1803', '0.2693', '-0.154', '-0.2368', '-0.8633', '0.3076', '-0.7734', '0.2524', '-0.1764', '0.1532', '0.1584', '-0.532', '-0.1233', '-1.413', '-0.07574', '0.785', '-0.01488', '0.4148', '0.1119', '-0.02994', '-0.1372', '-0.3108', '-0.502', '-0.06525', '0.1989', '0.08295', '-0.3848', '-0.32', '0.6045', '0.1779', '-0.3384', '-0.0148', '-0.042', '0.4849', '0.818', '0.07684', '0.2098', '0.036', '-0.1553', '0.00986', '-0.4612', '-0.1729', '-0.676', '0.05853', '0.2568', '-0.2627', '0.1886', '0.152', '-0.01521', '-0.621', '-0.2043', '0.202', '0.264', '-0.4922', '0.5396', '0.1259', '-0.2305', '-0.01254', '-0.2457', '0.4758', '0.1481', '-0.2203', '0.3137', '-0.4055', '0.1776', '0.3257', '-0.1332', '0.788', '0.677', '-0.594', '-0.2593', '-0.3115', '-0.2292', '0.5645', '-0.0904', '0.266', '-0.3848', '-0.58', '0.3599', '0.5527', '0.3872', '0.3013', '-0.06726', '0.02103', '0.4993']",,,C536416,,,,
mondo:0011664,immunodeficiency due to CD25 deficiency,"['immunodeficiency 41 with lymphoproliferation and autoimmunity', 'CD25 deficiency', 'IMD41', 'Interleukin 2 receptor, alpha, deficiency of', 'IL2RA deficiency', 'Interleukin-2 receptor alpha chain deficiency']",0111968,606367,169100,C1853392,"['-0.1804', '0.001411', '0.3855', '-0.3015', '0.01472', '-0.311', '0.1555', '0.05652', '-0.000446', '-0.1177', '0.2144', '0.0523', '-0.0719', '-0.10223', '0.05505', '-0.1698', '0.1265', '0.2037', '-0.2808', '-0.66', '-0.05698', '-0.2448', '0.414', '-0.203', '-0.09576', '0.03235', '-0.273', '0.0237', '0.007595', '-0.4653', '0.0424', '0.3242', '0.445', '0.2263', '0.0399', '-0.1732', '-0.2908', '-0.041', '-0.193', '-0.332', '-0.19', '-0.01926', '0.1774', '-0.132', '-0.3481', '-0.357', '0.001638', '-0.1936', '-0.004215', '0.1852', '-0.1852', '-0.0433', '0.3848', '-0.05716', '-0.2314', '-0.005386', '0.0703', '-0.404', '-0.2961', '0.031', '0.04102', '0.2512', '0.0713', '0.1407', '0.5366', '0.0818', '0.3533', '0.2196', '-0.354', '0.323', '-0.353', '-0.1656', '0.000316', '-0.1968', '0.12024', '-0.1538', '0.355', '0.101', '0.1296', '0.1677', '-0.2612', '0.04172', '-0.106', '0.2764', '-0.00306', '-0.1444', '0.3113', '0.2075', '0.356', '0.1326', '0.4265', '0.3442', '0.0081', '-0.0823', '0.5586', '0.5137', '0.223', '-0.3452', '0.0558', '0.1864']",,,C565232,,,,
mondo:0011667,maturity-onset diabetes of the young type 4,"['MODY4', 'PDX1 maturity-onset diabetes of the young (disease)', 'MODY insulin promoter factor-1 related', 'type 4 maturity-onset diabetes of the young', 'PDX1-associated monogenic diabetes', 'MODY, type IV', 'maturity-onset diabetes of the young, type 4', 'maturity onset diabetes of the Young, type 4', 'MODY type 4', 'diabetes mellitus MODY type 4', 'MODY, type 4']",0111103,606392,,,,C129746,,C563451,,,,
mondo:0011668,maturity-onset diabetes of the young type 6,"['maturity-onset diabetes of the young, type 6', 'type 6 maturity-onset diabetes of the young', 'neurogenic differentiation Factor 1-associated monogenic diabetes', 'MODY6', 'maturity-onset diabetes of the young 6', 'MODY, type 6', 'NEUROD1 maturity-onset diabetes of the young (disease)', 'MODY type 6', 'MODY NEUROD1 related', 'diabetes mellitus MODY type 6', 'NEUROD1-associated monogenic diabetes', 'maturity onset diabetes of the Young, type 6']",0111104,606394,,C1853371,,C129745,,C565231,,,,
mondo:0011669,hypotonia-cystinuria syndrome,"['hypotonia-cystinuria type 1 syndrome', 'homozygous 2P16 deletion syndrome', 'HCS', 'hypotonia-cystinuria syndrome type 1', 'homozygous 2P21 deletion syndrome', 'homozygous 2P16 deletion syndrome, formerly', 'cystinuria with mitochondrial disease', 'hypotonia-cystinuria syndrome']",0060858,606407,238517,CN226952,"['-0.138', '0.2925', '0.483', '-0.324', '0.2795', '-0.395', '-0.04736', '0.8696', '-0.3584', '0.1705', '-0.324', '0.1978', '0.1554', '-0.1073', '-0.297', '0.0626', '0.2097', '0.0563', '-0.4207', '-0.515', '-0.1465', '-0.3916', '0.3962', '-0.277', '0.0521', '-0.1666', '-0.2278', '-0.4463', '0.04788', '-0.2488', '0.2761', '0.0889', '0.7686', '0.3801', '-0.585', '-0.0635', '-0.2126', '0.1744', '-0.4575', '0.1888', '-0.0574', '-0.1426', '0.2886', '0.05054', '-0.0707', '-0.4194', '0.2389', '0.361', '-0.1395', '0.1437', '-0.2451', '-0.11456', '-0.1015', '-0.2837', '-0.09326', '-0.256', '0.164', '0.0844', '0.0829', '0.2803', '0.3093', '0.12415', '-0.1592', '-0.3347', '0.3306', '-0.1001', '0.4365', '0.1938', '-0.31', '0.09015', '-0.0639', '0.2556', '0.0426', '-0.3804', '-0.065', '-0.2583', '0.04294', '-0.0717', '-0.4736', '0.2335', '0.4084', '0.1299', '-0.4187', '-0.0374', '0.182', '0.2386', '0.2137', '0.1276', '0.6616', '0.0926', '0.393', '0.5493', '-0.03796', '-0.1052', '0.3809', '0.04105', '0.3044', '-0.258', '0.3877', '0.1979']",,0007550,C564710,,,,
mondo:0011670,Ehlers-Danlos syndrome due to tenascin-X deficiency,"['Ehlers-Danlos syndrome, classic-like type', 'Ehlers-Danlos-like syndrome due to tenascin-X deficiency', 'TNX deficiency', 'classical-like Ehlers-Danlos syndrome', 'Ehlers-Danlos syndrome, classic-like, 1', 'EDSCLL', 'EDS due to TNX deficiency', 'Tnx deficiency', 'Ehlers-Danlos syndrome, classic-like', 'clEDS', 'EDS, classic-like type', 'classical-like EDS', 'EDS due to Tnx deficiency', 'Ehlers-Danlos syndrome due to tenascin-X deficiency']",0080731,606408,230839,C1848029,"['0.48', '0.04938', '-0.3992', '0.269', '0.3684', '-0.6997', '-0.1266', '0.0612', '-0.9434', '0.452', '0.07806', '-0.1187', '-0.003338', '1.021', '-0.5576', '0.3628', '-0.518', '0.7295', '0.01169', '-0.4473', '-0.003313', '0.7954', '0.2559', '0.1808', '-0.365', '0.2037', '0.2617', '0.1635', '1.365', '0.3662', '1.055', '-0.8066', '-0.1214', '0.02716', '-0.1647', '-0.0965', '-0.8013', '0.1357', '0.3088', '-1.209', '0.5605', '-0.6377', '-0.912', '0.307', '0.135', '-0.522', '-0.4443', '0.864', '0.853', '-0.3772', '0.07605', '-0.2245', '0.636', '-0.03305', '0.1272', '-0.5586', '-0.632', '0.5547', '0.4954', '-0.1537', '-0.2568', '0.2499', '0.18', '-0.3018', '-0.12195', '0.447', '-0.4883', '0.717', '-0.405', '1.155', '-0.428', '0.1549', '-0.5815', '-0.4817', '-0.1015', '-0.2279', '-0.4893', '0.185', '0.369', '-0.03876', '-0.2399', '-0.6553', '0.2251', '0.4001', '-0.628', '-0.2788', '-0.03564', '0.918', '0.442', '0.154', '0.6274', '0.3962', '-0.2479', '0.6055', '0.7114', '0.1609', '0.612', '-0.3394', '-0.2102', '-0.1847']",,,C536193,,,,
mondo:0011671,Huntington disease-like 2,"['Huntington^s disease-like 2', 'HDL2', 'Huntington disease-like 2', 'Huntington disease-like type 2']",0090104,606438,98934,C1847987,"['-0.2391', '0.7236', '-0.816', '-0.286', '-0.284', '-0.577', '-0.1246', '0.723', '-0.4617', '-0.6235', '0.2322', '-0.1225', '-0.007675', '-0.3464', '1.014', '0.1775', '-0.07294', '-0.227', '0.2386', '-1.146', '0.10126', '-0.5005', '0.4426', '-0.2556', '0.466', '0.287', '-0.5137', '-0.01935', '0.2346', '0.417', '0.2554', '0.142', '0.518', '0.1151', '0.2106', '-0.03903', '-0.1606', '-0.629', '-0.1759', '-0.0462', '0.666', '-0.1523', '-0.2927', '-0.1315', '0.991', '-0.3093', '-0.716', '0.02567', '0.2052', '0.1603', '0.2563', '0.4106', '-0.4575', '-0.3286', '0.1158', '-0.03827', '0.541', '-0.3792', '-0.09045', '0.167', '-0.3093', '-0.152', '0.5317', '-0.3408', '-0.704', '0.0643', '0.114', '-0.04163', '-0.62', '0.462', '-0.08344', '-0.2854', '-0.01163', '0.856', '0.5903', '0.3606', '-0.08923', '0.1103', '-0.467', '-1.109', '0.547', '-0.4783', '0.101', '0.5396', '-0.565', '0.657', '0.491', '0.2927', '0.757', '0.1469', '0.2573', '0.004368', '0.0504', '0.5537', '0.6055', '0.3337', '-0.05353', '0.2527', '-0.1428', '0.2808']",,,C564708,,,,
mondo:0011672,persistent polyclonal B-cell lymphocytosis,"['persistent polyclonal B-cell lymphocytosis with binucleated lymphocytes', 'PPBL', 'persistent polyclonal B-cell lymphocytosis']",,606445,300324,C1847973,,,,C564707,,,,
mondo:0011673,autosomal dominant nonsyndromic hearing loss 30,"['deafness, autosomal dominant 30', 'autosomal dominant nonsyndromic deafness type 30', 'autosomal dominant nonsyndromic deafness 30', 'autosomal dominant deafness 30', 'DFNA30']",0110560,606451,,C1847972,,,,C564706,,,,
mondo:0011674,Charcot-Marie-Tooth disease dominant intermediate B,"['CMTDI1', 'CMTDIB', 'Charcot-Marie-Tooth disease, dominant Intermediate type B', 'Charcot-Marie-Tooth disease caused by mutation in DNM2', 'Charcot-Marie-Tooth disease, axonal, type 2M', 'DNM2-related intermediate Charcot-Marie-Tooth neuropathy', 'Charcot-Marie-Tooth neuropathy dominant intermediate B', 'Charcot-Marie-Tooth disease, axonal type 2M', 'Cmtdi1', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2M', 'Di-CMTB', 'Charcot-Marie-Tooth neuropathy, dominant Intermediate B', 'DI-CMTB', 'Charcot-Marie-Tooth neuropathy, dominant Intermediate B, with neutropenia', 'Charcot-Marie-Tooth neuropathy, axonal, type 2M', 'Charcot-Marie-Tooth disease dominant intermediate type B', 'Charcot-Marie-Tooth disease, dominant Intermediate B, with neutropenia', 'autosomal dominant intermediate Charcot-Marie-Tooth disease type B', 'Charcot-Marie-Tooth disease, dominant intermediate B', 'DNM2 Charcot-Marie-Tooth disease']",0110197,606482,100044,CN197338,"['0.10333', '0.182', '0.2512', '0.03787', '0.02783', '0.2244', '-0.2883', '0.6025', '-0.669', '-0.002604', '-0.1617', '0.1786', '-0.53', '0.2031', '-0.1', '-0.2246', '-0.06934', '-0.3523', '-0.416', '-0.4973', '0.11346', '0.3699', '0.3496', '0.775', '0.2778', '0.3894', '-0.0798', '0.05365', '0.1327', '-0.1459', '0.2605', '-0.5566', '0.3955', '0.4038', '0.47', '-0.8633', '-0.723', '-0.355', '0.325', '-0.2605', '-1.2705', '-0.2233', '-0.6445', '0.619', '-0.1691', '-0.1553', '-0.05276', '0.0923', '-0.1638', '-0.1421', '0.3142', '0.3103', '-0.2213', '-1.085', '0.1483', '-0.539', '-0.08026', '0.2512', '-0.8193', '-0.3738', '-0.3333', '0.176', '0.858', '0.9224', '-0.848', '0.935', '0.1004', '1.119', '-0.509', '0.593', '-0.8276', '0.05685', '0.4658', '-0.4153', '1.297', '0.3232', '-0.2676', '0.39', '0.1148', '-0.407', '-0.3667', '-0.1909', '0.7383', '0.6367', '-0.02855', '0.1316', '0.05762', '0.825', '1.045', '0.11456', '0.3167', '-0.004105', '-0.02542', '0.3232', '0.4375', '0.7583', '0.5415', '-0.4897', '-0.314', '0.498']",,,,,,,
mondo:0011675,"Charcot-Marie-Tooth Disease, axonal, type 2GG","['Charcot-Marie-Tooth disease, dominant intermediate A', 'Di-Cmta', 'autosomal dominant intermediate Charcot-Marie-Tooth disease type A', 'Charcot-Marie-Tooth disease dominant intermediate A', 'Charcot-Marie-Tooth disease dominant intermediate type A', 'CMTDIA', 'DI-CMTA', 'CMT2GG', 'Charcot-Marie-Tooth neuropathy dominant intermediate A', 'Charcot-Marie-Tooth neuropathy, dominant Intermediate a']",0110202,606483,100043,C1847896,,,,C564702,,,,
mondo:0011676,PHACE syndrome,"['pascual-Castroviejo type II syndrome', 'Posterior fossa brain malformations, hemangiomas of the face, arterial anomalies, cardiac anomalies, and eye abnormalities', 'Phaces association', 'P-CIIS', 'aortic aneurysm, giant congenital', 'pascual-Castroviejo syndrome type 2', 'PHACE association']",,606519,42775,C1847874,,,,,,,10068032,
mondo:0011677,Megarbane syndrome,"['short stature, abnormal face, joint laxity, hernias, delayed bone age, and severe psychomotor retardation', 'Megarbane syndrome']",,606527,,C1847871,,,,C536145,,,,
mondo:0011678,homozygous 11P15-p14 deletion syndrome,"['hyperinsulinism, infantile, with enteropathy and deafness', 'chromosome 11p15-p14 deletion syndrome', 'homozygous 11P15-p14 deletion syndrome']",,606528,,C1847866,,,,C564701,,,,
mondo:0011679,"craniosynostosis syndrome, autosomal recessive","['craniosynostosis, autosomal recessive', 'autosomal recessive craniosynostosis', 'craniosynostosis syndrome, autosomal recessive']",,606529,,C1847865,,,,C564700,,,,
mondo:0011680,autosomal recessive congenital ichthyosis 3,"['autosomal recessive congenital ichthyosis type 3', 'ichthyosis, congenital, autosomal recessive type 3', 'ichthyosis, lamellar, 5, formerly', 'ichthyosis, congenital, autosomal recessive 3', 'collodion baby, self-healing', 'lamellar ichthyosis 5', 'ARCI3', 'ichthyosis, lamellar, 5']",0060711,606545,,,,,,C564699,,,,
mondo:0011681,episodic ataxia type 4,"['ataxia, periodic vestibulocerebellar', 'EA4', 'PATX', 'episodic ataxia, type 4', 'periodic vestibulocerebellar ataxia']",0050992,606552,79136,C1847843,,,,C564698,,,,
mondo:0011682,episodic ataxia type 3,"['EA3', 'episodic ataxia-vertigo-tinnitus-myokymia syndrome', 'episodic ataxia, type 3', 'ataxia, episodic, with vertigo and tinnitus']",0050991,606554,79135,C1847839,,,,C564697,,,,
mondo:0011683,oculocutaneous albinism type 4,"['OCA4', 'albinism, oculocutaneous, type IV', 'oculocutaneous albinism caused by mutation in SLC45A2', 'albinism, oculocutaneous, type 4', 'oculocutaneous albinism type IV', 'oculocutaneous albinism, type 4', 'SLC45A2 oculocutaneous albinism']",0070098,606574,79435,C1847836,"['0.4841', '0.1705', '-0.3997', '0.11487', '0.5825', '-0.07874', '-0.3003', '0.3613', '-0.008545', '-0.581', '0.62', '-0.089', '0.199', '0.7676', '-0.545', '0.308', '0.3572', '-0.1289', '0.76', '-0.8774', '-0.8022', '0.08856', '0.6875', '-0.4114', '-0.11505', '-0.1799', '-0.6235', '-3.57e-05', '0.6733', '0.1392', '0.2974', '0.0819', '0.3328', '0.673', '-0.12256', '0.273', '-0.9375', '-0.844', '0.2937', '-0.3948', '1.056', '-0.302', '-0.2622', '0.008934', '-0.2054', '-0.727', '0.5117', '-0.989', '0.762', '0.08234', '-0.2284', '-0.5103', '0.09094', '-0.10016', '0.528', '0.43', '0.3335', '1.007', '-0.10114', '-0.94', '-0.2391', '0.429', '0.7275', '0.5', '-0.2764', '0.143', '0.314', '0.771', '-0.10706', '0.574', '-0.08057', '0.171', '-0.01439', '-0.3472', '0.7056', '0.17', '0.006435', '-0.3186', '0.1956', '-0.568', '0.7065', '-0.572', '0.21', '0.3423', '-0.3882', '-1.412', '0.5107', '0.5127', '0.757', '0.302', '0.05127', '0.881', '-0.1283', '-0.05994', '0.536', '0.393', '-0.4888', '-0.208', '0.1969', '0.4856']",,,C564696,,,,
mondo:0011684,vitiligo-associated multiple autoimmune disease susceptibility 1,"['vitiligo-associated multiple autoimmune disease susceptibility 1', 'systemic lupus erythematosus, vitiligo-related', 'vitiligo-associated multiple autoimmune disease susceptibility type 1', 'VAMAS1', 'vitiligo']",,606579,247871,C1847835,,,,,,,,
mondo:0011685,"polysubstance abuse, susceptibility to","['drug addiction, susceptibility to', 'polysubstance abuse, susceptibility to', 'PSAB']",,606581,,,,,,,,,,
mondo:0011686,DNA ligase IV deficiency,"['DNA ligase IV deficiency', 'LIG4 syndrome', 'ligase 4 syndrome']",0060021,606593,99812,C1847827,"['0.2888', '0.2151', '0.453', '-0.6543', '-0.10986', '-0.004814', '-0.006996', '0.515', '-0.145', '-0.3147', '0.3154', '0.01006', '0.504', '-0.4265', '-0.2546', '0.008064', '0.05984', '-0.2512', '-0.1997', '-0.6777', '-0.0316', '-0.2488', '0.4922', '-0.2129', '-0.2087', '0.0476', '-0.4514', '-0.05652', '-0.1334', '-0.4998', '-0.04102', '0.4792', '0.6797', '0.421', '0.37', '0.6147', '-0.02347', '-0.406', '-0.5073', '-0.3135', '0.548', '-0.1049', '-0.04623', '-0.03247', '-0.03998', '-0.4045', '-0.2076', '-0.2238', '-0.363', '-0.619', '0.03445', '-0.3162', '0.3', '0.496', '0.1029', '-0.293', '-0.165', '0.0898', '-0.4807', '0.0167', '0.2566', '-0.2177', '0.10706', '-0.06573', '0.1984', '-0.1837', '0.1415', '0.1744', '-0.4885', '0.933', '-0.4417', '0.513', '0.09296', '0.637', '0.3774', '0.34', '-0.2976', '-0.3467', '0.3364', '0.1808', '0.2676', '0.5107', '-0.2017', '0.4163', '-1.017', '-0.2854', '0.7236', '0.8164', '-0.0159', '0.2249', '0.721', '0.01868', '-0.2162', '-0.02701', '0.583', '0.8994', '-0.0972', '-0.9326', '0.344', '0.10864']",C122657,,C564694,,,,
mondo:0011687,Charcot-Marie-Tooth disease axonal type 2F,"['Charcot-Marie-Tooth disease type 2 caused by mutation in HSPB1', 'CMT 2F', 'HSPB1 Charcot-Marie-Tooth disease type 2', 'Charcot-Marie-Tooth disease type 2F', 'Charcot-Marie-Tooth disease, axonal, type 2F', 'Charcot-Marie-Tooth neuronal type 2F', 'Charcot-Marie-Tooth disease, neuronal, type 2F', 'CMT2F', 'Charcot-Marie-Tooth neuropathy type 2F', 'Charcot Marie Tooth disease type 2F', 'Charcot-Marie-Tooth neuropathy, type 2F', 'autosomal dominant Charcot-Marie-Tooth disease type 2F']",0110163,606595,99940,C4304675,"['-0.0368', '0.5054', '0.0661', '-0.1346', '-0.06635', '-0.1606', '-0.149', '1.012', '-0.9727', '0.1598', '-0.07416', '0.5107', '-0.4724', '0.1854', '-0.2576', '-0.6772', '-0.2998', '-0.5903', '0.02983', '-0.5854', '-0.2079', '0.2996', '0.3547', '0.3809', '0.2108', '0.7954', '-0.2637', '0.3567', '-0.248', '0.1207', '0.07806', '-0.3855', '-0.00957', '0.2347', '0.02322', '-0.8066', '-0.5527', '-0.1812', '0.4822', '-0.2253', '-1.323', '-0.4458', '-0.4082', '0.393', '-0.0679', '-0.0925', '-0.1024', '0.06445', '-0.3064', '0.0795', '0.2372', '0.4648', '-0.511', '-0.9053', '0.567', '-0.2844', '0.1445', '0.0987', '-0.325', '0.012665', '-0.4072', '-0.03802', '0.8994', '0.891', '-0.816', '1.138', '0.2488', '0.7', '-0.6416', '0.5044', '-0.693', '0.1471', '0.623', '-0.02754', '1.485', '0.4531', '-0.3972', '0.6343', '0.3367', '-0.1686', '-0.1644', '0.09204', '1.016', '0.4646', '0.2854', '0.0573', '0.3083', '0.633', '0.857', '0.1309', '0.0653', '-0.1523', '0.306', '0.372', '0.306', '0.615', '0.7646', '-0.6597', '-0.3147', '0.3997']",,,C535413,,,,
mondo:0011688,muscular dystrophy-dystroglycanopathy type B5,"['congenital muscular dystrophy 1C', 'muscular dystrophy, congenital, FKRP-related', 'muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5', 'MDDGB5', 'MDC1C', 'FKRP-related congenital muscular dystrophy', 'congenital muscular dystrophy-FKRP related', 'muscular dystrophy, congenital, 1C', 'muscular dystrophy-dystroglycanopathy (congenital with or without intellectual disability), type B, 5']",0110635,606612,52428,C1847759,"['-0.05475', '0.0699', '0.0192', '-0.03287', '0.0726', '-0.1354', '0.008965', '0.0704', '-0.1186', '-0.02327', '-0.04843', '-0.03714', '-0.015366', '0.01066', '-0.01949', '-0.04163', '0.01743', '-0.06934', '-0.0361', '-0.1393', '-0.01089', '-0.04114', '0.07574', '0.0129', '-0.006855', '-0.03867', '0.01536', '-0.05984', '0.01161', '-0.05222', '0.0799', '0.003422', '0.099', '0.03528', '0.05502', '-0.04626', '-0.00958', '-0.01793', '0.007236', '-0.11127', '-0.002728', '-0.0968', '-0.002687', '0.02222', '-0.0554', '-0.0461', '0.01782', '0.0912', '0.02693', '0.02908', '-0.02127', '-0.0441', '0.00928', '-0.00441', '-0.04056', '-0.07104', '0.08606', '-0.02803', '-0.1024', '0.02663', '0.0285', '0.02016', '0.02466', '0.01492', '-0.01407', '0.008446', '0.0991', '0.0786', '-0.09033', '0.03104', '-0.09155', '0.001291', '0.0371', '-0.06335', '0.0776', '0.06015', '-0.02061', '-0.02805', '-0.0738', '-0.03004', '0.0328', '0.01901', '-0.05225', '0.07056', '-0.04172', '0.0145', '0.01545', '0.1168', '0.11145', '0.0073', '0.014824', '0.0627', '0.03485', '0.02663', '0.1672', '0.04593', '0.10425', '-0.1191', '-0.02663', '0.01643']",,,C564691,,,,
mondo:0011689,"dyslexia, susceptibility to, 6","['DYX6', 'dyslexia, susceptibility to, 6']",,606616,,,,,,,,,,
mondo:0011690,"Camurati-Engelmann disease, type 2","['Camurati-Engelmann disease, type 2', 'CAEND2', 'Camurati Engelmann disease, type 2', 'progressive diaphyseal dysplasia with striations of the bones']",,606631,,C2931683,,,,C537978,,,,
mondo:0011691,amyotrophic lateral sclerosis type 3,"['amyotrophic lateral sclerosis 3', 'ALS3']",0060195,606640,,,,,,C564688,,,,
mondo:0011693,"glaucoma, normal tension, susceptibility to","['NTG', 'glaucoma, normal tension, susceptibility to', 'glaucoma, normal pressure, susceptibility to']",,606657,,,,,,,,,,
mondo:0011694,spinocerebellar ataxia type 15/16,"['spinocerebellar ataxia type 15/16', 'spinocerebellar ataxia type 15', 'SCA15/16', 'SCAR16', 'spinocerebellar ataxia 15', 'SCA16 (formerly)', 'spinocerebellar ataxia 16', 'spinocerebellar ataxia 16, formerly', 'spinocerebellar ataxia type 16', 'SCA15', 'spinocerebellar ataxia 16 (formerly)']",0050966,606658,98770,CN229296,"['-0.03035', '-0.2646', '-0.01645', '0.09406', '-0.2408', '-1.015', '0.415', '0.2698', '-0.605', '-1.085', '0.2974', '0.2544', '-0.0883', '0.0843', '0.6807', '-0.2136', '-0.0898', '-0.503', '0.0667', '-0.8843', '-0.2083', '-0.3772', '0.1813', '-0.773', '0.617', '-0.5786', '-0.3174', '0.08545', '-0.1211', '-0.7407', '0.2314', '0.368', '-0.4438', '-0.2054', '0.3708', '0.08026', '0.0495', '0.0422', '0.2769', '0.4636', '0.4211', '0.26', '-0.4675', '0.4863', '0.6797', '-0.5664', '0.03662', '0.3835', '0.3186', '-0.0755', '-0.0719', '0.0673', '0.01633', '-0.577', '0.1403', '-0.7324', '0.2727', '0.5034', '-0.07776', '0.399', '-0.661', '0.3733', '0.1814', '-0.3022', '-0.3555', '0.4546', '0.2217', '0.863', '-0.5947', '0.5063', '0.8594', '0.422', '-0.08295', '-0.7197', '0.778', '0.4158', '0.2184', '0.1787', '0.01191', '0.561', '-0.1278', '-0.917', '0.621', '0.555', '-0.3713', '-0.5435', '0.2964', '0.03793', '0.836', '0.3865', '0.476', '0.4849', '-0.007656', '-0.0998', '1.129', '0.944', '0.3354', '0.3003', '-0.3472', '-0.11035']",C150250,,C564685,,,,
mondo:0011695,"melanoma, uveal, susceptibility to, 1","['melanoma, uveal, susceptibility to, type 1', 'UVM1', 'melanoma, uveal, susceptibility to, 1']",,606660,,,,,,,,,,
mondo:0011696,"melanoma, uveal, susceptibility to, 2","['UVM2', 'melanoma, uveal, susceptibility to, type 2', 'melanoma, uveal, susceptibility to, 2']",,606661,,,,,,,,,,
mondo:0011697,Waardenburg syndrome type 2C,"['WS2C', 'Waardenburg syndrome, type 2C', 'Waardenburg syndrome type IIC']",0110951,606662,,C1847722,,,,C564684,,,,
mondo:0011698,glycine N-methyltransferase deficiency,"['hypermethioninemia due to glycine N-methyltransferase deficiency', 'Glycine N-methyltransferase deficiency', 'hypermethioninemia due to GNMT deficiency', 'glycine N-methyltransferase deficiency', 'GNMT deficiency']",0111037,606664,289891,C1847720,"['-0.6533', '0.255', '-0.64', '-0.2983', '0.2146', '-0.0999', '-0.3652', '0.1569', '-0.2051', '0.3052', '-0.2617', '0.123', '0.536', '-0.13', '0.01768', '-0.2009', '0.3503', '-0.2139', '-0.78', '-0.7285', '0.1511', '0.0733', '0.3723', '0.11383', '0.1917', '0.1279', '0.3354', '0.0455', '0.1458', '0.3047', '0.64', '-0.0766', '0.5522', '0.1265', '-0.366', '-0.5015', '-0.1901', '-0.4924', '0.4226', '-0.3184', '-0.01174', '-0.5264', '0.3782', '-0.49', '-0.6245', '-0.2903', '0.388', '-0.3838', '0.0679', '0.07587', '0.0999', '0.03308', '-0.603', '-0.07153', '-0.297', '0.4565', '0.04733', '-0.3467', '-0.1459', '0.237', '0.3323', '-0.0474', '0.28', '-0.28', '0.063', '0.6367', '-0.06152', '0.362', '-0.443', '-0.0933', '-0.0196', '0.2825', '-0.0009284', '0.002075', '0.1979', '0.1097', '0.4846', '0.09393', '0.1433', '-0.0156', '-0.06174', '0.0479', '-0.358', '-0.2922', '-0.07135', '0.3774', '-0.162', '0.4275', '0.884', '0.2764', '0.505', '0.1638', '-0.761', '-0.1312', '0.762', '0.792', '0.3962', '-0.5654', '-0.2766', '-0.1224']",,,,,,,
mondo:0011699,inflammatory bowel disease 8,"['inflammatory bowel disease type 8', 'IBD8', 'inflammatory bowel disease 8']",0110904,606668,,C1847719,,,,C564682,,,,
mondo:0011700,inflammatory bowel disease 6,"['inflammatory bowel disease type 6', 'IBD6', 'inflammatory bowel disease 6']",0110907,606674,,C1847692,,,,C564681,,,,
mondo:0011701,inflammatory bowel disease 4,"['IBD4', 'inflammatory bowel disease 4', 'inflammatory bowel disease type 4']",0110903,606675,,C1847691,,,,C564680,,,,
mondo:0011702,dilated cardiomyopathy 1L,"['dilated cardiomyopathy type 1L', 'cardiomyopathy, dilated, 1L', 'SGCD familial isolated dilated cardiomyopathy', 'CMD1L', 'cardiomyopathy, dilated, type 1L', 'familial isolated dilated cardiomyopathy caused by mutation in SGCD']",0110436,606685,,C1847667,,,,C564679,,,,
mondo:0011703,spongiform encephalopathy with neuropsychiatric features,['spongiform encephalopathy with neuropsychiatric features'],,606688,,C1847650,,,,C564678,,,,
mondo:0011705,lymphangioleiomyomatosis,"['lung lymphangioleiomyomatosis', 'lymphangioleiomyomatosis', 'lymphangio-myomatosis', 'LAM', 'lymphangioleiomyomatosis, somatic', 'pulmonary lymphangioleiomyomatosis', 'lymphangiomyomatosis']",,606690,,,,C3725,,D018192,,J84.81,,
mondo:0011706,Kufor-Rakeb syndrome,"['Kufor-Rakeb syndrome', 'autosomal recessive juvenile onset Parkinson disease 9', 'KRS', 'autosomal recessive Parkinson disease 9', 'PARK9', 'Pallidopyramidal degeneration with supranuclear upgaze paresis, and dementia', 'ceroid lipofuscinosis, neuronal, 12', 'Pallidopyramidal Degeneration with supranuclear upgaze paresis and dementia', 'Parkinson disease 9, autosomal recessive', 'park 9', 'Parkinson disease 9, autosomal recessive, juvenile-onset', 'Parkinson disease type 9', 'KRPPD']",0060556,606693,306674,,"['-0.275', '0.2874', '0.0731', '-0.2101', '0.1904', '-0.6387', '-0.0862', '0.1328', '-0.2783', '0.02988', '-0.1993', '-0.134', '-0.0741', '-0.601', '0.4697', '-0.4011', '-0.0382', '-0.4678', '-0.3833', '-0.4954', '0.1769', '-0.3062', '0.0008082', '0.1526', '0.2856', '0.06287', '-0.02171', '-0.162', '-0.249', '0.2559', '0.2181', '0.3188', '0.282', '-0.07355', '0.3096', '-0.1719', '-0.0894', '-0.377', '-0.02684', '-0.1608', '0.6045', '-0.61', '-0.003443', '0.08435', '0.1799', '-0.421', '-0.08655', '0.2703', '0.2747', '-0.1279', '0.0605', '0.2654', '-0.3704', '0.1539', '0.0796', '-0.2627', '0.2688', '-0.2236', '-0.3867', '0.2717', '0.1655', '-0.0686', '0.428', '-0.176', '-0.1487', '0.2167', '0.2866', '0.1798', '-0.1974', '0.2522', '-0.5654', '-0.4133', '-0.2338', '0.0392', '0.05176', '0.0678', '0.2522', '0.376', '-0.51', '-0.1923', '0.1858', '-0.567', '-0.04828', '0.6104', '-0.1718', '-0.3008', '0.1616', '0.449', '0.4807', '0.03052', '0.453', '0.0919', '0.0088', '-0.2313', '0.5767', '0.395', '0.3591', '-0.0789', '0.266', '0.1945']",,,C537177,,,,
mondo:0011708,autosomal dominant nonsyndromic hearing loss 36,"['autosomal dominant nonsyndromic deafness type 36', 'deafness, autosomal dominant 36', 'deafness, autosomal dominant type 36', 'autosomal dominant deafness 36', 'DFNA36', 'TMC1 autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness 36', 'autosomal dominant nonsyndromic deafness caused by mutation in TMC1']",0110563,606705,,C1847626,,,,C564675,,,,
mondo:0011709,split hand-foot malformation 5,"['split-hand/foot malformation 5', 'SHFM5', 'split hand-foot malformation type 5', 'split-hand/foot malformation type 5']",0090022,606708,,C1847622,,C75002,,C564674,,,,
mondo:0011710,specific language impairment 1,"['specific language impairment QTL, 1', 'SLI1', 'specific language impairment quantitative trait locus on chromosome 16', 'specific language impairment 1']",,606711,,C1847614,,,,,,,,
mondo:0011711,specific language impairment 2,"['specific language impairment QTL, 2', 'specific language impairment 2', 'SLI2', 'specific language impairment quantitative trait locus on chromosome 19']",,606712,,C1847605,,,,,,,,
mondo:0011712,van der Woude syndrome 2,"['Van Der Woude syndrome type 2', 'van der Woude syndrome caused by mutation in GRHL3', 'VAN DER Woude syndrome 2', 'GRHL3 van der Woude syndrome', 'van der Woude syndrome 2', 'VWS2']",,606713,,C1847604,,,,C536529,,,,
mondo:0011713,melanoma-pancreatic cancer syndrome,"['melanoma-pancreatic cancer syndrome', 'familial atypical multiple Mole melanoma-pancreatic carcinoma syndrome']",,606719,,,,C176904,,C563985,,,,
mondo:0011714,"partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome","['LCCNS', 'lipodystrophy, partial, with congenital cataracts and neurodegeneration', 'partial lipodystrophy, congenital cataracts, and neurodegeneration syndrome', 'lipodystrophy, familial partial, type 7']",,606721,,C3807567,,,,,,,,
mondo:0011715,Seckel syndrome 2,"['Seckel syndrome type 2', 'Seckel syndrome 2', 'RBBP8 Seckel syndrome', 'Seckel-type dwarfism 2', 'microcephalic primordial dwarfism 2', 'SCKL2', 'Seckel syndrome caused by mutation in RBBP8']",0070013,606744,,C1847572,,,,C537534,,,,
mondo:0011716,acute hemorrhagic leukoencephalitis,"['acute hemorrhagic encephalomyelitis', 'Weston-Hurst syndrome', 'acute necrotizing hemorrhagic leukoencephalitis', 'AHL', 'Ahl', 'AHLE', 'acute hemorrhagic leukoencephalitis', 'acute haemorrhagic leucoencephalitis of Weston Hurst']",10992,606752,,C0014077,,C84535,0007132,D004684,136.9,,,
mondo:0011717,hyperinsulinism-hyperammonemia syndrome,"['hyperinsulinism hyperammonemia syndrome', 'hyperinsulinism-hyperammonemia syndrome', 'hyperinsulinemic hypoglycemia, familial, 6', 'GLUD1 hyperinsulinism', 'glutamate dehydrogenase 1 hyperinsulinism', 'hyperinsulinism/hyperammonemia syndrome', 'HA/hi syndrome', 'hi/HA syndrome', 'GDH hyperinsulinism', 'HHF6', 'hyperinsulinemic hypoglycemia, familial, type 6', 'hyperinsulinemic hypoglycemia familial 6']",0070217,606762,35878,C1847555,"['0.2847', '0.304', '-0.7876', '-0.1294', '-0.5825', '-0.03516', '0.1554', '0.581', '0.2646', '-0.007397', '-0.2534', '-0.2527', '0.4324', '-0.003464', '-0.05707', '0.07935', '0.3892', '-0.3232', '0.08295', '-0.2979', '0.4', '-0.03827', '0.182', '0.11304', '-0.4905', '-0.267', '-0.678', '-0.432', '0.595', '-0.2664', '0.4075', '0.4104', '0.4944', '0.2461', '-0.807', '0.0627', '-0.4536', '0.2223', '-0.3696', '0.3108', '0.3125', '-0.2856', '0.3157', '0.2717', '-0.2598', '-0.0956', '-0.2119', '-0.0549', '0.2333', '0.5776', '-0.01802', '0.1978', '-0.1366', '-0.4634', '-0.04727', '0.755', '0.695', '-0.549', '-0.3506', '0.524', '-0.397', '0.262', '0.313', '-0.634', '0.3455', '0.1672', '0.4238', '0.4858', '-0.6704', '0.3733', '-0.2374', '0.5933', '0.3984', '-0.2167', '0.1434', '0.3333', '-0.04352', '-0.1975', '-0.1062', '-0.1334', '0.04095', '-0.257', '-0.4834', '-0.0975', '0.162', '0.4517', '0.0863', '0.48', '1.387', '0.6763', '0.614', '0.951', '-0.07806', '0.04672', '0.05566', '0.4768', '0.3', '-0.8833', '0.196', '0.3198']",C131832,,C538375,,,,
mondo:0011718,primary ciliary dyskinesia 2,"['primary ciliary dyskinesia caused by mutation in DNAAF3', 'ciliary dyskinesia, primary, type 2', 'ciliary dyskinesia, primary, 2', 'primary ciliary dyskinesia type 2', 'DNAAF3 primary ciliary dyskinesia', 'primary ciliary dyskinesia 2 with or without situs inversus', 'ciliary dyskinesia, primary, 2, with or without situs inversus', 'CILD2']",0110626,606763,,C1847554,,,,C535277,,,,
mondo:0011719,gastrointestinal stromal tumor,"['gastrointestinal stromal tumours', 'stromal tumour of gastrointestinal tract', 'gist', 'gastrointestinal stromal tumour (gist)', 'gastrointestinal stromal tumor (gist)', 'gastrointestinal stromal tumors', 'gastrointestinal stromal tumor', 'gastrointestinal stromal sarcoma', 'stromal tumor of gastrointestinal tract', 'gant', 'gastrointestinal stromal neoplasm', 'gastrointestinal stromal tumor, familial, isolated cases', 'gastrointestinal stromal tumor, isolated cases']",9253,606764,44890,C3179349,"['-0.0646', '-0.172', '0.05917', '-0.01421', '0.2307', '0.12134', '0.2086', '0.2566', '-0.1586', '-0.04227', '0.01227', '0.319', '-0.4321', '0.1359', '-0.482', '-0.2764', '-0.136', '-0.1857', '0.2532', '-0.506', '0.1144', '-0.5312', '0.1936', '-0.1537', '0.1676', '0.0006704', '-0.185', '0.179', '0.2279', '-0.02335', '0.593', '-0.5806', '0.1921', '-0.07446', '0.1844', '0.3145', '-0.815', '0.1324', '-0.1302', '0.2847', '0.04398', '-0.2025', '0.3318', '-0.3955', '0.302', '-0.1967', '-0.1704', '0.05338', '0.252', '0.3833', '-0.06726', '0.5293', '-0.2974', '-0.247', '-0.2281', '0.2522', '-0.1008', '-0.2117', '-0.3196', '0.2288', '0.1678', '0.1721', '-0.2737', '-0.269', '-0.008255', '0.1437', '0.2605', '0.1981', '0.1433', '0.487', '0.3333', '0.0984', '-0.2421', '-0.255', '0.1858', '0.03955', '0.2102', '0.2103', '0.1499', '-0.609', '-0.668', '-0.2769', '-0.086', '-0.1736', '0.04047', '-0.0918', '0.373', '0.02083', '0.3035', '-0.3674', '-0.1178', '0.1647', '0.2568', '-0.2876', '1.162', '0.11835', '0.0732', '-0.1753', '-0.2637', '0.05487']",C3868,,D046152,,,10051066,
mondo:0011720,spermatogenic failure 3,"['SPGF3', 'azoospermia caused by mutation in SLC26A8', 'spermatogenic failure 3', 'spermatogenic failure type 3', 'SLC26A8 azoospermia']",0070168,606766,,C1847540,,,,C564665,,,,
mondo:0011721,distal myopathy with anterior tibial onset,"['DMAT', 'distal anterior compartment myopathy', 'myopathy, distal, with anterior tibial onset']",0111187,606768,178400,C1847532,"['-0.587', '-0.1722', '-0.1738', '-0.2286', '0.083', '-0.564', '-0.152', '0.784', '-1.022', '-0.2734', '-0.3962', '0.5703', '0.3586', '-0.07434', '0.2217', '-0.2498', '-0.19', '0.05212', '-0.4714', '-0.71', '0.424', '-0.0717', '0.1301', '0.426', '0.2793', '0.1824', '0.05884', '-0.05676', '-0.2098', '0.04855', '0.771', '0.419', '0.01514', '-0.1901', '0.3208', '-0.09314', '-0.1326', '0.1537', '0.3813', '-0.3782', '-0.2717', '-0.528', '-0.07874', '0.3682', '-0.2646', '0.05447', '-0.188', '0.2103', '0.1761', '0.2656', '-0.3909', '0.11395', '-0.1829', '-0.2496', '-0.3086', '-0.647', '0.3726', '-0.2157', '-0.1586', '-0.1211', '0.2983', '0.2451', '0.04846', '-0.1167', '-0.2888', '0.333', '0.185', '0.8247', '-0.5337', '-0.0248', '-0.06726', '-0.0851', '0.2325', '0.3193', '0.6196', '-0.2532', '0.128', '0.02428', '0.00346', '-0.2303', '0.05972', '0.1702', '0.6465', '0.2563', '-0.4424', '0.0678', '-0.1647', '0.463', '0.655', '0.03732', '0.4043', '-0.1946', '0.1823', '-0.04742', '0.547', '-0.1389', '0.4546', '-0.3289', '-0.4648', '0.0496']",,,C564664,,,,
mondo:0011722,intellectual disability-obesity-prognathism-eye and skin anomalies syndrome,"['Momes syndrome', 'MOMES syndrome', 'intellectual disability, obesity, mandibular prognathism, and eye and skin anomalies', 'mental retardation, obesity, mandibular prognathism, and eye and skin anomalies']",,606772,397973,C1847522,,,,C564660,,,,
mondo:0011723,hemifacial myohyperplasia,"['HMH', 'hemifacial myohyperplasia', 'hypertrophy and asymmetry of the facial muscles']",,606773,141148,,,,,C535862,744.89,,,
mondo:0011724,encephalopathy due to GLUT1 deficiency,"['G1D', 'GLUT1DS1', 'De Vivo disease', 'GLUT1 deficiency syndrome 1, autosomal recessive', 'GLUT1-DS', 'GLUT1 deficiency syndrome type 1', 'GLUT1 deficiency syndrome', 'glucose transporter type 1 deficiency syndrome', 'glut-1 deficiency syndrome', 'glucose transporter type 1 deficiency', 'glucose transporter protein syndrome', 'glucose transporter Protein syndrome', 'glucose transport defect, blood-brain barrier', 'glucose transporter type1 (glut-1) deficiency', 'encephalopathy due to GLUT1 deficiency', 'GLUT1 deficiency syndrome 1', 'GLUT1 deficiency syndrome 1, infantile onset, severe', 'glucose TRANSPORT defect, blood-brain barrier GLUT1 deficiency syndrome 1, autosomal recessive, included', 'GLUT1 DS', 'glucose Transport defect, blood-brain barrier']",,606777,71277,CN030711,"['-0.03516', '0.5073', '-0.2488', '-0.1874', '0.03284', '-0.2695', '0.4636', '0.4238', '-0.356', '-0.01141', '-0.1635', '0.3257', '0.1888', '-0.1097', '0.315', '-0.326', '0.2069', '-0.3403', '-0.4463', '-0.5107', '0.04248', '-0.2175', '0.1583', '-0.2712', '-0.11707', '-0.2292', '0.1782', '0.1178', '-0.4258', '0.2954', '0.0976', '0.2698', '0.2798', '0.0698', '-0.2388', '0.2194', '0.0889', '0.001297', '-0.2092', '0.053', '0.08636', '-0.2842', '0.263', '0.06445', '-0.1361', '-0.3284', '-0.011696', '0.03192', '-0.06113', '0.06287', '-0.02528', '0.1335', '-0.2408', '-0.336', '0.218', '0.1164', '0.4192', '-0.02275', '-0.0787', '0.2473', '-0.05615', '-0.04614', '0.5137', '-0.0607', '0.01231', '-0.013504', '0.552', '0.0334', '-0.3867', '0.2046', '-0.064', '0.425', '0.209', '-0.3696', '-0.1519', '0.1575', '0.3887', '0.2129', '-0.3625', '0.002651', '0.1412', '0.02986', '-0.1826', '-0.2153', '0.08386', '-0.04376', '0.2344', '0.3376', '0.617', '-0.0674', '0.353', '0.53', '0.04807', '-0.1368', '-0.02318', '0.3816', '0.302', '-0.2786', '0.3098', '0.3003']",,0009139,C536830,,,,
mondo:0011725,Crigler-Najjar syndrome type 2,"['Crigler-Najjar syndrome, type 2', 'Arias syndrome', 'hereditary unconjugated hyperbilirubinemia type 2', 'bilirubin-UGT deficiency type 2', 'bilirubin uridinediphosphate glucuronosyltransferase deficiency type 2', 'UGT deficiency type 2', 'hyperbilirubinemia, Crigler-Najjar type 2', 'Crigler Najjar syndrome, type 2', 'Crigler-Najjar syndrome, type II']",,606785,79235,C2931132,"['0.03934', '0.1942', '-0.4404', '-0.2651', '0.126', '0.06445', '-0.3308', '0.624', '-0.10126', '-0.307', '0.1718', '0.2284', '0.04617', '0.2473', '0.322', '-0.316', '0.2388', '0.2457', '0.2654', '-0.5522', '-0.156', '-0.4258', '0.867', '0.1565', '0.0082', '-0.05124', '-0.1395', '0.0322', '-0.2825', '0.1329', '0.04678', '0.1812', '0.4824', '0.06433', '-0.5625', '0.05923', '-0.0934', '-0.458', '0.57', '0.287', '0.3882', '-0.3923', '0.1384', '0.3745', '-0.1719', '-0.03427', '-0.1289', '0.131', '0.1126', '0.1349', '0.06934', '-0.11035', '-0.01383', '-0.6084', '-0.2551', '0.8257', '0.8037', '0.1221', '-0.7056', '0.2201', '0.0523', '0.596', '1.029', '-0.12476', '0.2634', '0.1324', '0.5044', '0.3018', '-0.8228', '-0.06216', '0.04657', '0.1484', '0.0636', '0.003038', '0.642', '0.402', '0.606', '-0.05115', '-0.5513', '0.0196', '-0.01816', '0.1694', '-0.1984', '-0.14', '0.1355', '0.318', '0.1283', '0.2954', '0.1346', '0.2257', '1.306', '0.682', '0.09735', '-0.3333', '0.539', '0.311', '0.1746', '-0.4912', '-0.2496', '0.3755']",,,C536213,,,10011387,
mondo:0011726,peripheral arterial occlusive disease 1,"['peripheral arterial occlusive disease type 1', 'Paod1', 'peripheral arterial occlusive disease 1']",,606787,,C1847493,,,,C564658,,,,
mondo:0011727,"anorexia nervosa, susceptibility to, 1","['anon', 'ANON1', 'anorexia nervosa, susceptibility to', 'anorexia nervosa, susceptibility to, 1', 'AN']",,606788,,CN244557,,,,,,,,
mondo:0011728,blepharospasm,"['benign essential blepharospasm', 'BEB', 'blepharospasm, benign essential', 'blepharospasm, benign essential, susceptibility to', 'blepharospasm, primary benign']",529,606798,,C0005747,,,,D001764,333.81,G24.5,,
mondo:0011729,"stroke, susceptibility to, 1","['Strk1', 'stroke, susceptibility to, type 1', 'stroke, susceptibility to, 1']",,606799,,,,,,,,,,
mondo:0011730,fumaric aciduria,"['FMRD', 'fumarate hydratase deficiency', 'fumaric aciduria', 'fumarase deficiency']",0111261,606812,24,C2936826,"['0.10895', '0.02545', '-0.0744', '-0.2573', '-0.537', '-0.3728', '0.2335', '0.806', '-0.683', '-0.8086', '-0.003796', '-0.355', '-0.2177', '-0.1342', '0.0919', '0.06775', '0.2788', '-0.407', '-0.5483', '-0.5425', '0.06726', '0.1396', '0.02092', '0.0494', '0.00873', '-0.3086', '-0.3723', '-0.3281', '-0.2603', '-0.2632', '-0.08044', '0.4502', '0.556', '0.1628', '-0.293', '-0.06854', '-0.11926', '-0.4937', '-0.2181', '0.132', '0.4575', '-0.1948', '0.2484', '-0.0882', '0.04773', '-0.08765', '-0.2766', '-0.4233', '-0.0488', '0.3083', '-0.1869', '-0.1891', '-0.2119', '0.0901', '-0.3909', '0.1293', '-0.0886', '-0.02713', '0.1698', '0.9136', '0.1431', '-0.0815', '0.2834', '-0.02148', '-0.2556', '0.006588', '0.2257', '0.4575', '-0.765', '0.4321', '0.254', '0.3623', '-0.65', '-0.2786', '0.336', '0.2086', '0.349', '-0.5938', '-0.2482', '-0.143', '0.1786', '0.0867', '-0.282', '0.5728', '-0.307', '0.6396', '0.3152', '-0.3813', '0.626', '0.1287', '0.1193', '-0.01602', '-0.325', '0.4866', '0.3125', '0.781', '0.01453', '-0.3604', '0.6357', '-0.01909']",,,C538191,282.3,,,
mondo:0011731,glucose-galactose malabsorption,"['Complex carbohydrate intolerance', 'GGM', 'monosaccharide malabsorption', 'glucose galactose malabsorption deficiency', 'SGLT1 deficiency', 'carbohydrate intolerance of glucose galactose', 'glucose/galactose malabsorption']",,606824,35710,,"['-0.4915', '0.421', '-0.0716', '-0.02846', '-0.191', '-0.2524', '-0.547', '0.214', '-0.0433', '-0.1755', '-0.1869', '-0.1794', '-0.05103', '0.312', '-0.3774', '-0.4897', '0.0629', '0.04266', '-0.11755', '-0.4045', '0.1495', '-0.7046', '0.545', '-0.4622', '0.1885', '0.2358', '0.1534', '-0.0421', '0.2954', '-0.4272', '0.2135', '0.1855', '0.4307', '0.258', '-0.1864', '0.1287', '-0.1447', '-0.1622', '-0.3225', '0.01219', '-0.232', '-0.2954', '0.2078', '-0.11646', '-0.1454', '-0.1981', '0.1398', '-0.01245', '0.3916', '0.671', '-0.0749', '0.05252', '-0.01294', '-0.3054', '-0.013664', '-0.312', '0.1511', '-0.2998', '-0.097', '0.4075', '0.03049', '-0.0408', '0.165', '-0.27', '0.1644', '-0.2238', '0.321', '0.2944', '-0.3967', '0.2266', '-0.3186', '-0.10284', '0.1719', '-0.2917', '-0.0256', '-0.06714', '0.3245', '-0.0462', '-0.02425', '-0.01576', '0.1525', '-0.402', '-0.2688', '-0.01484', '0.24', '0.0881', '0.2441', '-0.243', '0.501', '0.1144', '0.378', '0.1191', '0.1484', '0.1646', '0.3118', '0.4583', '0.2402', '-0.2483', '0.3098', '0.09503']",,,C562602,271.3,,10066388,
mondo:0011732,familial digital arthropathy-brachydactyly,"['digital arthropathy-brachydactyly, familial', 'FDAB']",,606835,85169,C1847406,"['-0.435', '0.1573', '-0.0957', '-0.0061', '0.1686', '-0.646', '-0.1342', '0.5483', '-0.439', '-0.1803', '-0.245', '0.5645', '0.0509', '-0.125', '-0.074', '-0.179', '0.168', '0.0773', '0.1721', '-0.4275', '0.1392', '0.215', '0.1041', '-0.05905', '0.10345', '0.4487', '0.2737', '0.269', '0.06052', '-0.474', '0.2747', '-0.388', '-0.2445', '-0.0506', '-0.00526', '-0.3206', '0.10583', '-0.5063', '-0.04828', '-0.3025', '0.012245', '-0.2866', '0.1837', '0.1998', '0.04086', '-0.1952', '-0.1781', '0.2136', '-0.01287', '-0.02779', '-0.08466', '-0.11316', '0.00446', '-0.1097', '0.2307', '-0.5366', '0.4895', '0.2229', '-0.12036', '-0.0006247', '0.3342', '0.0972', '-0.2096', '0.0337', '0.03046', '0.1465', '0.11707', '0.4795', '-0.309', '0.08923', '-0.3242', '-0.2303', '0.1946', '-0.003305', '0.2969', '0.304', '-0.1191', '0.535', '-0.1633', '-0.009445', '0.00328', '0.3735', '0.09375', '0.1503', '0.1458', '0.212', '0.06464', '0.674', '0.1101', '-0.2686', '-0.1908', '0.07983', '0.3748', '-0.1094', '0.513', '-0.1313', '0.4385', '-0.7334', '0.03125', '-0.0804']",C175208,,C564656,,,,
mondo:0011733,"parasomnia, sleep bruxism type","['parasomnia, Sleeptalking type', 'parasomnia, sleep bruxism type', 'PSMNSB', 'faciomandibular myoclonus, nocturnal', 'nocturnal facio-mandibular myoclonus']",,606840,,,,,,C536389,,,,
mondo:0011734,Cardioneuromyopathy with hyaline masses and nemaline rods,['Cardioneuromyopathy with hyaline masses and nemaline rods'],,606842,,C1847387,,,,C564655,,,,
mondo:0011735,hyper-IgM syndrome type 3,"['hyper IgM syndrome 3', 'immunodeficiency with hyper IgM type 3', 'hyper-IgM syndrome 3', 'CD40 hyper-IgM syndrome', 'immunodeficiency with hyper-IgM, type 3', 'type 3 hyper-IgM immunodeficiency', 'CD40 deficiency', 'hyper-IgM syndrome due to CD40 deficiency', 'immunodeficiency with hyper-IgM type 3', 'HIGM3', 'hyper-IgM syndrome caused by mutation in CD40']",0060023,606843,101090,,"['-0.2366', '0.478', '0.1589', '0.1627', '0.1887', '-0.1098', '-0.0917', '-0.147', '-0.0125', '-0.1642', '-0.04883', '0.02788', '0.03802', '0.0761', '0.02855', '-0.2886', '-0.07104', '-0.1271', '-0.02919', '-0.1026', '0.012955', '-0.2886', '0.474', '0.04678', '0.3335', '0.02263', '0.1228', '-0.05298', '0.02696', '-0.1847', '0.09625', '0.279', '0.379', '-0.04147', '-0.01046', '-0.1985', '-0.0765', '0.1368', '0.02621', '-0.404', '-0.11206', '-0.369', '-0.0857', '0.0387', '-0.492', '-0.3545', '0.04062', '-0.12286', '0.3662', '-0.1552', '0.2115', '-0.4692', '-0.03842', '0.1025', '-0.3237', '0.01866', '0.2783', '-0.09424', '-0.3408', '0.3745', '-0.06415', '0.193', '0.166', '0.03342', '0.2107', '0.1055', '0.2908', '0.03015', '-0.3003', '0.2458', '-0.129', '-0.05957', '0.1002', '0.0401', '0.2411', '0.1237', '-0.06305', '0.1313', '-0.1327', '-0.1301', '-0.01329', '-0.099', '-0.03412', '-0.04938', '-0.4138', '-0.11694', '0.2568', '0.53', '0.3516', '0.085', '0.1792', '0.3591', '-0.03029', '-0.1854', '0.4463', '0.2917', '0.118', '-0.678', '-0.2688', '0.284']",,,,,,,
mondo:0011736,Cree intellectual disability syndrome,"['Cree intellectual disability syndrome', 'Cree mental retardation syndrome']",,606851,,C1847361,,,,C564654,,,,
mondo:0011737,parkinson disease 10,"['Parkinson disease 10', 'PARK10', 'Parkinson disease, Age at onset of']",,606852,,C1847360,,,,C564653,,,,
mondo:0011738,bilateral frontoparietal polymicrogyria,"['polymicrogyria, bilateral frontoparietal', 'cerebellar ataxia with neuronal migration defect', 'BFPP']",0080922,606854,101070,C1847352,"['-0.485', '0.1768', '0.1389', '-0.7705', '-0.274', '-0.4248', '0.333', '0.252', '-0.65', '-0.00527', '-0.714', '-0.3818', '-0.0359', '-0.2052', '0.0947', '-0.05295', '0.3113', '-0.8325', '0.03102', '-0.84', '0.03262', '0.05566', '-0.1243', '-0.4724', '0.2637', '-0.2395', '0.11597', '-0.3057', '-0.1026', '0.0677', '-0.393', '0.735', '0.4983', '-3.43e-05', '0.1519', '0.00381', '-0.4365', '0.1146', '-0.657', '-0.2795', '0.7417', '-0.5386', '0.03366', '0.2979', '0.1854', '-0.3362', '0.1329', '0.3376', '0.3545', '-0.321', '0.1909', '0.3865', '-0.1643', '-0.248', '-0.1565', '0.1931', '0.422', '0.1063', '-0.6133', '0.558', '-0.005325', '0.10645', '0.5356', '-0.0459', '-0.684', '0.02191', '0.4612', '0.3257', '-0.517', '0.0624', '-0.3948', '0.9326', '0.4897', '-0.3828', '-0.1389', '0.28', '0.4773', '0.0715', '-0.1702', '-0.1915', '-0.1384', '-0.3887', '-0.02293', '0.3074', '-0.1672', '-0.12366', '-0.1605', '0.4238', '0.325', '-0.01639', '0.1735', '0.9043', '0.1247', '0.1361', '0.4458', '0.1267', '0.5176', '-0.228', '0.568', '0.2852']",C148367,,C564652,,,,
mondo:0011739,"pancreatic cancer, susceptibility to, 1","['pancreatic cancer, susceptibility to, type 1', 'pancreatic cancer, susceptibility to, 1', 'familial pancreatic carcinoma caused by mutation in PALLD', 'Pnca1', 'PALLD familial pancreatic carcinoma', 'susceptibility to pancreatic cancer 1']",,606856,,,,,,,,,,
mondo:0011740,Carney-Stratakis syndrome,"['Carney-Stratakis dyad', 'paraganglioma and gastrointestinal stromal tumor', 'Carney-Stratakis syndrome', 'paraganglioma and gastrointestinal stromal tumour', 'paraganglioma and gastric stromal sarcoma', 'Carney dyad', 'Carney-Stratakis dyad of paraganglioma and gastric stromal sarcoma', 'gist-paraganglioma dyad', 'paraganglioma and gist']",0080533,606864,97286,C1847319,"['-0.1959', '0.0461', '-0.196', '-0.01102', '-0.1326', '0.777', '0.732', '0.471', '-0.336', '0.1674', '-0.11487', '-0.0856', '-0.519', '0.1815', '0.425', '-0.1156', '0.1106', '-0.1169', '-0.0825', '-0.4812', '0.09106', '-0.4106', '0.1533', '-0.294', '0.137', '-0.238', '-0.4712', '0.4795', '-0.2786', '-0.1425', '0.6333', '0.0739', '0.11694', '-0.1493', '-0.1232', '0.007145', '-0.3452', '-0.1247', '-0.06058', '-0.1555', '-0.0417', '-0.496', '0.4353', '-0.8804', '0.672', '-0.0959', '-0.6465', '-0.303', '0.2046', '0.1432', '-0.3533', '-0.05704', '-0.2441', '0.0486', '-0.3723', '0.3196', '0.07574', '0.4646', '-0.005547', '0.4646', '0.677', '0.0629', '-0.1316', '0.168', '-0.1072', '0.0753', '0.1469', '0.4514', '-0.1815', '0.3936', '0.4075', '-0.1039', '0.2266', '0.1433', '0.5977', '-0.0735', '0.1398', '0.514', '-0.2866', '-0.9185', '-0.1708', '0.198', '0.587', '0.5674', '-0.8164', '-0.305', '0.5625', '0.2445', '0.1586', '-0.1782', '0.1646', '-0.1287', '0.02698', '0.03595', '1.234', '0.0404', '0.2637', '-0.509', '0.1722', '0.2006']",C94831,,C564650,,,,
mondo:0011741,"Hirschsprung disease, susceptibility to, 6","['HSCR6', 'Hirschsprung disease, susceptibility to, 6']",,606874,,,,,,,,,,
mondo:0011742,"Hirschsprung disease, susceptibility to, 7","['Hirschsprung disease, susceptibility to, 7', 'HSCR7']",,606875,,,,,,,,,,
mondo:0011743,Alzheimer disease 4,"['AD4', 'Alzheimer^s disease 4', 'Alzheimer disease type 4', 'Alzheimer disease, familial4', 'Alzheimer disease-4', 'familial Alzheimer^s disease, type 4', 'Alzheimer disease familial type 4', 'Alzheimer disease, familial, 4', 'Alzheimer disease 4', 'familial Alzheimer disease, type 4', 'Alzheimer^s disease type 4', 'Ad4']",0110040,606889,,C1847200,,C123413,,C536596,,,,
mondo:0011744,primary intraosseous venous malformation,"['osseous venous malformation', 'intraosseous hemangioma', 'vascular malformation, primary intraosseous', 'hemangioma, intraosseous', 'vascular malformation osseous']",,606893,140436,C1847197,"['-0.644', '-0.4514', '0.1519', '-0.2922', '0.0427', '0.06915', '0.0566', '0.10675', '-0.679', '0.1266', '-0.4487', '-0.1547', '0.2097', '-0.0375', '-0.508', '-0.2148', '0.11334', '-0.2788', '-0.1937', '-0.3696', '0.2583', '-0.2177', '0.1162', '-0.518', '0.633', '0.08466', '-0.3032', '0.117', '0.7817', '0.288', '-0.01518', '0.2008', '0.2463', '-0.06384', '0.1401', '0.2039', '-0.05322', '0.1788', '0.1351', '-0.6636', '0.1326', '-0.002047', '0.5083', '-0.5312', '0.2803', '-0.0663', '-0.1393', '0.1971', '0.2235', '0.2512', '0.0544', '0.3625', '0.2341', '0.3125', '-0.6255', '-0.1534', '0.01584', '-0.2947', '-0.2458', '0.4138', '0.0746', '0.2136', '-0.4353', '-0.3586', '0.1517', '-0.05865', '0.3318', '0.5283', '-0.1539', '0.48', '-0.4001', '0.5527', '0.1453', '-0.1919', '-0.2152', '-0.15', '0.665', '0.1854', '-0.1026', '-0.1201', '-0.283', '-0.4749', '0.0891', '0.464', '-0.514', '0.0679', '0.203', '0.1371', '0.327', '-0.02652', '-0.376', '0.65', '0.276', '0.1798', '0.9673', '0.0396', '0.3896', '-0.339', '0.5605', '-0.2103']",,,C564648,,,,
mondo:0011745,"duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery","['duodenojejunal atresia with volvulus, absent dorsal mesentery, and absent superior mesenteric artery', 'duodenojejunal atresia with volvulus, absent dorsal mesentery and absent superior mesenteric artery']",,606894,,C1847196,,,,C535722,,,,
mondo:0011746,"symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch","['symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch', 'distal symphalangism, hypoplastic carpal bones, microdontia, dental pulp stones, and narrowing of the zygomatic arch']",,606895,,C1847185,,,,C538148,,,,
mondo:0011747,"dyslexia, susceptibility to, 5","['DYX5', 'dyslexia, susceptibility to, 5']",,606896,,,,,,,,,,
mondo:0011748,Usher syndrome type 1G,"['USHER syndrome, type Ig', 'USH1G Usher syndrome', 'Usher syndrome type Ig', 'Usher syndrome, type 1G', 'USH1G', 'Usher syndrome caused by mutation in USH1G']",0110834,606943,,C1847089,,,,C564643,,H35.5,,
mondo:0011749,oculocutaneous albinism type 1B,"['oculocutaneous albinism, Amish type', 'Yellow oculocutaneous albinism', 'albinism, oculocutaneous, type I, temperature-sensitive', 'oculocutaneous albinism type IB', 'Yellow mutant albinism', 'platinum oculocutaneous albinism', 'oculocutaneous albinism, type 1B', 'albinism, oculocutaneous, type IB', 'OCA1B', 'albinism, oculocutaneous, type 1B', 'albinism, Yellow mutant type', 'Oca1-Ts', 'Yellow albinism']",0070095,606952,79434,C1847132,"['0.4248', '0.2361', '-0.3672', '0.2334', '0.4124', '-0.1321', '-0.1173', '0.4067', '-0.0332', '-0.7847', '0.615', '-0.2109', '-0.1349', '0.7095', '-0.5815', '0.4158', '0.6064', '-0.3735', '0.8286', '-0.87', '-0.9395', '0.2659', '0.5586', '-0.362', '-0.2861', '-0.1158', '-0.653', '0.1401', '0.5767', '0.1598', '0.5425', '0.072', '0.4143', '0.667', '0.04858', '0.4937', '-0.8047', '-0.6875', '0.2544', '-0.2126', '1.195', '-0.141', '-0.0634', '0.0343', '-0.263', '-0.749', '0.5386', '-0.9224', '0.973', '0.0432', '-0.05453', '-0.4714', '0.03296', '-0.2246', '0.405', '0.4167', '0.3445', '0.714', '-0.1517', '-1.217', '-0.4175', '0.2289', '0.493', '0.2856', '-0.1482', '0.177', '0.5537', '0.8096', '-0.146', '0.7354', '-0.0003698', '0.5044', '0.003014', '-0.3154', '0.7876', '0.0854', '-0.1663', '-0.4785', '0.159', '-0.6196', '0.693', '-0.6074', '0.3257', '0.377', '-0.455', '-1.228', '0.4175', '0.573', '0.984', '0.2932', '0.351', '0.938', '-0.2856', '-0.0861', '0.4678', '0.098', '-0.64', '-0.1492', '0.3206', '0.7017']",,,C537729,,,,
mondo:0011751,"COPD, severe early onset","['COPD, severe early-onset', 'COPD', 'COPD, rate of decline of lung function in', 'pulmonary disease, chronic obstructive', 'pulmonary disease, chronic obstructive, severe early-onset']",,,,,,,,,,,,
mondo:0011752,nephronophthisis 4,"['nephronophthisis 4', 'NPHP4 nephronophthisis (disease)', 'NPHP4', 'nephronophthisis type 4', 'juvenile nephronophthisis 4', 'nephronophthisis 4, juvenile']",0111115,606966,,C2959367,,,,C564640,,,,
mondo:0011753,"epilepsy, idiopathic generalized, susceptibility to, 2","['epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 14', 'epilepsy, idiopathic generalized, susceptibility to, 2', 'EIG2']",0111317,606972,,,,,,,,,,
mondo:0011754,familial hyperreninemic hypoaldosteronism type 2,"['hyperreninemic hypoaldosteronism, familial, 2', 'FHHA2', 'aldosterone synthase deficiency unrelated to CYP11B2', 'aldosterone synthase deficiency unrelated to the aldosterone synthase gene', 'Fhha2', 'hyperreninemic hypoaldosteronism, familial, type 2']",,606984,99764,C1846990,,,,C564638,,,,
mondo:0011755,senior-loken syndrome 3,"['SENIOR-Loken syndrome 3', 'SLSN3']",,606995,,C1846980,,,,C564637,,,,
mondo:0011756,Senior-Loken syndrome 4,"['SLSN4', 'Senior-Loken syndrome 4', 'Senior-Loken syndrome caused by mutation in NPHP4', 'Senior-Loken syndrome type 4', 'NPHP4 Senior-Loken syndrome', 'SENIOR-Loken syndrome 4']",,606996,,C1846979,,,,C537581,,,,
mondo:0011757,brachydactyly type A1B,"['brachydactyly, type A1, B', 'BDA1B']",0110974,607004,,C1846949,,,,C564635,,,,
mondo:0011758,Hurler syndrome,"['MPS1H', 'mucopolysaccharidosis type 1H', 'MPS I H', 'MPS1-H', 'Hurler syndrome', 'MPSIH', 'mucopolysaccharidosis IH', 'mucopolysaccharidosis type IH', 'Hurler disease']",0111390,607014,93473,,"['-0.1648', '0.422', '0.1971', '-0.0812', '0.1099', '-0.02481', '0.6484', '1.075', '-0.939', '-0.1022', '-0.412', '-0.0387', '0.235', '0.0703', '-0.6885', '-0.8765', '-0.01039', '-0.1185', '-0.3064', '-0.2905', '0.2177', '-0.2388', '0.359', '-0.5005', '0.325', '-0.3008', '-0.07776', '0.2856', '-0.2208', '0.0946', '0.7104', '0.634', '0.06323', '-0.1576', '-0.03207', '-0.2869', '-0.2852', '-0.3767', '0.41', '-0.0774', '0.2423', '-0.2385', '0.594', '0.6577', '0.2715', '0.222', '-0.2878', '-0.0751', '-0.4639', '-0.02461', '0.005997', '0.2089', '-0.1863', '-0.05487', '0.831', '-0.3977', '-0.2158', '0.561', '0.1561', '-0.0664', '-0.2291', '0.0615', '-0.731', '-0.1254', '0.004517', '-0.752', '0.2235', '-0.4424', '-0.4937', '0.3289', '-0.4148', '-0.177', '-0.04678', '-0.04', '0.2754', '0.0721', '0.04855', '-0.2656', '-0.9165', '-0.3694', '-0.1987', '-0.8013', '-0.4226', '0.5312', '-0.4507', '0.4316', '-0.0736', '-0.1263', '0.4705', '-0.0746', '0.248', '0.2233', '0.797', '0.1458', '0.699', '0.3174', '0.2708', '-0.5884', '0.6045', '-0.1787']",C61261,,,,,,
mondo:0011759,Hurler-Scheie syndrome,"['MPSIH/S', 'mucopolysaccharidosis type 1H/S', 'Hurler-Scheie syndrome', 'mucopolysaccharidosis type Ih/S', 'mucopolysaccharidosis type IH/S', 'mucopolysaccharidosis IH/S', 'Hurler–Scheie syndrome', 'MPS1-HS', 'MPS1H/S', 'MPS I H-S']",0111389,607015,93476,C0086431,"['0.079', '0.4392', '0.3857', '-0.01566', '0.2186', '0.2727', '0.1881', '0.8867', '-0.626', '0.1334', '-0.3555', '0.0476', '0.1759', '0.787', '0.314', '-0.723', '-0.3313', '-0.4324', '-0.2383', '-0.4888', '-0.1693', '-0.02104', '0.987', '-0.3352', '0.701', '-0.1713', '0.002548', '0.3843', '-0.2932', '0.1433', '0.6606', '0.2896', '-0.1185', '0.2246', '-0.1113', '-0.769', '-0.1292', '-0.4666', '0.1815', '-0.04755', '0.3948', '-0.217', '0.568', '0.2031', '0.2114', '0.2081', '0.01187', '-0.3767', '-0.333', '-0.2499', '-0.2281', '-0.1416', '0.1333', '0.1213', '0.534', '-0.4727', '-0.4954', '-0.1232', '-0.141', '0.3306', '0.078', '-0.2115', '-0.3484', '-0.2454', '-0.1976', '-0.667', '0.1581', '0.06494', '-0.4492', '0.08923', '-0.633', '-0.6763', '-0.1536', '-0.4622', '0.1656', '0.2218', '-0.4905', '-0.297', '-0.6235', '-0.3374', '0.2255', '-0.5728', '-0.547', '0.854', '-0.631', '0.1414', '0.4194', '0.0979', '0.3125', '0.1422', '0.04263', '0.3457', '0.1694', '-0.04004', '0.3796', '0.3506', '0.004158', '-0.5566', '0.2131', '-0.319']",C122782,,,,,10056916,
mondo:0011760,Scheie syndrome,"['mucopolysaccharidosis type IS', 'MPS I S', 'mucopolysaccharidosis type V, formerly', 'mucopolysaccharidosis type 1S', 'MPSIS', 'MPS V', 'mucopolysaccharidosis Is', 'MPS5, formerly', 'mucopolysaccharidosis type V', 'Scheie syndrome', 'MPS V, formerly', 'MPS1-S', 'MPS1S']",0060222,607016,93474,C0026708,"['0.1537', '0.338', '0.45', '-0.003672', '0.0362', '0.02254', '0.1865', '0.7534', '-0.6943', '-0.5015', '-0.07404', '0.1312', '-0.1222', '0.299', '0.2009', '-0.5366', '-0.357', '-1.03', '-0.032', '-0.3008', '0.2396', '-0.0799', '0.521', '-0.01788', '-0.0606', '-0.06476', '0.1744', '0.3115', '0.253', '0.2593', '0.09906', '0.464', '0.02376', '0.1691', '-0.2932', '-0.6733', '0.136', '-0.633', '0.5815', '0.1771', '0.285', '-0.2927', '0.4377', '0.7935', '0.11847', '0.3484', '-0.1674', '-0.1432', '0.1829', '-0.1558', '-0.08746', '0.07416', '0.2375', '-0.067', '0.02908', '-0.542', '-0.04797', '0.065', '0.10223', '0.118', '0.2896', '0.5034', '-0.1412', '-0.1813', '0.0751', '-0.3198', '0.2153', '0.00366', '-0.1658', '0.05716', '-0.4983', '-0.1776', '-0.297', '-0.3071', '0.2754', '0.4207', '-0.5024', '0.1653', '-0.565', '-0.4712', '-0.263', '-0.3875', '-0.6074', '0.71', '-0.3232', '0.384', '0.2451', '0.02878', '0.5903', '0.2096', '0.05167', '0.6226', '0.198', '-0.1118', '0.1644', '0.1843', '-0.001115', '-0.658', '0.1595', '0.1943']",C61265,,,,,,
mondo:0011761,autosomal dominant nonsyndromic hearing loss 21,"['deafness, autosomal dominant 21', 'DFNA21', 'autosomal dominant deafness 21', 'autosomal dominant nonsyndromic deafness 21', 'autosomal dominant nonsyndromic deafness type 21']",0110551,607017,,C1846922,,,,C564634,,,,
mondo:0011762,autosomal recessive nonsyndromic hearing loss 22,"['autosomal recessive nonsyndromic deafness 22', 'autosomal recessive deafness 22', 'autosomal recessive nonsyndromic deafness type 22', 'deafness, autosomal recessive type 22', 'OTOA autosomal recessive nonsyndromic deafness', 'DFNB22', 'deafness, autosomal recessive 22', 'autosomal recessive nonsyndromic deafness caused by mutation in OTOA']",0110480,607039,,C1846896,,,,C564633,,,,
mondo:0011764,autosomal dominant Parkinson disease 8,"['Parkinson disease 8, autosomal dominant', 'autosomal dominant Parkinson disease type 8', 'PARK8', 'LRRK2 Parkinson disease', 'Parkinson disease 8', 'Parkinson disease caused by mutation in LRRK2', 'autosomal dominant Parkinson^s disease 8']",0060371,607060,,C1846862,,,,,,,,
mondo:0011765,multiple epiphyseal dysplasia type 5,"['Microepiphyseal dysplasia, bilateral hereditary', 'bilateral hereditary micro-epiphyseal dysplasia', 'multiple epiphyseal dysplasia, MATN3 related', 'multiple epiphyseal dysplasia, MATN3-related', 'MED5', 'epiphyseal dysplasia multiple 5', 'multiple epiphyseal dysplasia 5', 'MATN3 multiple epiphyseal dysplasia (disease)', 'BHMED', 'Polyepiphyseal dysplasia type 5', 'epiphyseal dysplasia, multiple, type 5', 'EDM5', 'epiphyseal dysplasia, multiple, 5']",0070299,607078,93311,C4275060,"['-0.678', '0.2054', '0.2744', '-0.5713', '0.5835', '-0.649', '-0.2052', '0.4353', '-0.783', '-0.1293', '-0.1545', '0.555', '0.2712', '-0.3145', '0.1203', '0.358', '0.2744', '0.187', '-0.355', '-0.5146', '-0.1555', '0.1198', '0.403', '-0.3674', '-0.01558', '0.586', '0.1565', '-0.2134', '0.02734', '0.006935', '0.1455', '-0.0471', '0.1637', '0.1387', '0.115', '0.0932', '-0.2598', '-0.567', '-0.005524', '-0.357', '0.1736', '-0.4302', '-0.086', '0.2034', '-0.031', '-0.362', '-0.2668', '0.3926', '0.11316', '-0.3997', '0.1294', '0.1714', '0.01671', '-0.05573', '-0.1957', '-0.8022', '0.1276', '-0.1779', '-0.2229', '-0.1971', '0.675', '-0.048', '-0.324', '-0.0803', '-0.2998', '0.0389', '0.4868', '0.3784', '-0.2347', '0.1305', '-0.3547', '-0.2861', '0.010635', '-0.6387', '0.1279', '0.086', '-0.3508', '0.511', '-0.2917', '-0.288', '0.1132', '0.3225', '0.0591', '0.1525', '-0.349', '0.003635', '0.03293', '0.669', '0.1262', '0.01442', '-0.2457', '0.3206', '0.1116', '0.3076', '0.4136', '0.2603', '0.687', '-0.3115', '0.323', '0.1484']",,,C535505,,Q77.3,,
mondo:0011766,"46,XY gonadal dysgenesis-motor and sensory neuropathy syndrome","['46,XY gonadal dysgenesis, partial, with MINIFASCICULAR neuropathy', '46XY gonadal dysgenesis with minifascicular neuropathy']",,607080,168563,C2751325,"['-0.3796', '0.01134', '0.2585', '-0.4407', '0.1164', '-0.0888', '-0.007084', '0.418', '-0.2644', '0.06976', '-0.0719', '-0.309', '-0.09564', '0.0592', '-0.1101', '-0.0566', '0.2347', '-0.1399', '0.03705', '-0.652', '-0.03384', '-0.2487', '0.1458', '-0.010056', '0.1165', '-0.01472', '0.1587', '0.297', '-0.2487', '-0.487', '0.2524', '-0.00892', '0.7686', '-0.11694', '-0.1169', '-0.3992', '0.1401', '-0.117', '-0.3865', '-0.3232', '0.12415', '-0.002356', '-0.4011', '0.2059', '-0.0644', '-0.1405', '-0.366', '0.1345', '-0.01746', '0.571', '-0.00754', '0.0797', '-0.1443', '0.0325', '-0.0881', '0.03284', '0.4514', '-0.497', '-0.5005', '0.2428', '-0.006237', '0.064', '0.258', '0.3186', '-0.4788', '0.302', '0.2451', '0.5913', '-0.1494', '0.2664', '-0.12427', '0.2', '0.0822', '-0.07495', '0.4084', '-0.459', '0.12335', '0.3677', '-0.1901', '-0.2776', '-0.1956', '0.3528', '0.4082', '0.2683', '-0.1659', '-0.1553', '-0.0959', '-0.012794', '0.0774', '-0.2979', '0.2234', '0.3008', '0.1425', '-0.3267', '0.571', '-0.3972', '0.4175', '-0.1974', '-0.1677', '0.3545']",,,C567773,,,,
mondo:0011767,autosomal recessive nonsyndromic hearing loss 31,"['autosomal recessive nonsyndromic deafness type 31', 'DFNB31', 'autosomal recessive deafness 31', 'autosomal recessive nonsyndromic deafness caused by mutation in WHRN', 'autosomal recessive nonsyndromic deafness 31', 'whirler, mouse, homolog of', 'deafness, autosomal recessive type 31', 'WHRN autosomal recessive nonsyndromic deafness', 'deafness, autosomal recessive 31']",0110490,607084,,C1846839,,,,C564629,,,,
mondo:0011768,myasthenia gravis with thymus hyperplasia,"['myasthenia gravis with thymus hyperplasia', 'Myas1']",,607085,,C1846838,,,,C564628,,,,
mondo:0011770,"aortic aneurysm, familial thoracic 2","['FAA2', 'AAT2', 'aortic aneurysm, familial thoracic 2']",,607087,,C1846837,,,,C564627,,,,
mondo:0011771,distal spinal muscular atrophy type 3,"['dSMA3', 'neuronopathy, distal hereditary motor, type 4', 'HMN 3', 'dHMN3', 'dHMN4', 'distal hereditary motor neuropathy type 3 and type 4', 'spinal muscular atrophy, chronic distal, autosomal recessive', 'spinal muscular atrophy, distal, autosomal recessive, 3', 'HMN 4', 'dHMN3 and dHMN4', 'neuropathy, distal hereditary motor, type 4', 'autosomal recessive distal spinal muscular atrophy type 3', 'neuronopathy, distal hereditary motor, type 3']",0111211,607088,139547,C1846823,,,,C564626,,,,
mondo:0011772,B4GALT1-congenital disorder of glycosylation,"['B4GALT1-CDG', 'congenital disorder of glycosylation type IId', 'carbohydrate deficient glycoprotein syndrome type IId', 'congenital disorder of glycosylation, type IId', 'congenital disorder of glycosylation type 2d', 'CDG IId', 'Beta-1,4-galactosyltransferase deficiency', 'CDG syndrome type IId', 'CDG 2D', 'CDG-IId', 'CDG2D', 'B4GALT1-CDG (CDG-IId)']",0070256,607091,79332,C2931009,"['-0.768', '0.06445', '0.02621', '-0.1427', '0.3232', '-0.602', '-0.1288', '0.2551', '-0.253', '-0.211', '0.04755', '-0.2123', '0.1449', '-0.1903', '-0.1359', '-0.01401', '0.07367', '-0.191', '-0.5684', '-0.5073', '0.2329', '0.00845', '0.4468', '-0.3833', '-0.06088', '-0.00784', '-0.1947', '-0.0404', '0.04288', '-0.205', '0.2002', '0.1125', '0.3748', '0.1195', '0.002235', '-0.514', '0.2595', '-0.3152', '-0.1265', '-0.2427', '0.01689', '-0.2903', '-0.07886', '-0.02199', '-0.1017', '-0.1296', '0.2947', '0.07983', '-0.2698', '-0.09174', '-0.03702', '-0.1771', '0.10034', '0.2883', '-0.3408', '-0.4668', '0.6294', '0.0734', '-0.2207', '0.43', '0.03802', '0.0895', '0.5527', '0.1396', '-0.0689', '-0.2351', '0.181', '0.08136', '-0.9478', '-0.2156', '-0.3154', '0.4702', '0.02399', '0.2937', '-0.0014', '0.1456', '0.413', '-0.1876', '-0.3638', '0.11334', '0.0727', '0.4084', '0.01564', '0.4377', '0.12256', '0.2076', '0.11786', '0.716', '0.3247', '-0.2886', '0.2012', '0.6187', '0.0436', '-0.3677', '0.693', '0.1001', '0.417', '-0.4915', '0.3909', '0.1615']",,,C535753,,,,
mondo:0011773,anauxetic dysplasia,"['anauxetic dysplasia 1', 'spondylometaepiphyseal dysplasia Menger type', 'spondylometaepiphyseal dysplasia, Menger type', 'spondylometaepiphyseal dysplasia anauxetic type', 'ANXD1', 'anauxetic dysplasia type 1', 'spondyloepimetaphyseal dysplasia, Menger type', 'spondyloepimetaphyseal dysplasia, anauxetic type', 'anauxetic dysplasia', 'spondylometaepiphyseal dysplasia, anauxetic type']",0080942,,93347,CN029084,"['-0.0818', '0.2115', '0.371', '-0.543', '0.361', '-0.3152', '-0.155', '0.712', '-0.5024', '-0.6694', '0.2455', '0.1624', '-0.3167', '0.2607', '-0.13', '0.11755', '0.2297', '-0.1658', '-0.3384', '-0.4705', '0.0841', '0.0886', '0.1827', '-0.3438', '0.0718', '0.1812', '0.0719', '-0.1766', '0.6567', '-0.413', '0.00862', '-0.1592', '0.1251', '0.3264', '0.224', '-0.09467', '-0.1714', '-0.4688', '0.1998', '-0.2264', '-0.09454', '-0.3545', '-0.1481', '0.1724', '-0.02379', '-0.349', '0.1065', '0.2328', '0.2512', '-0.11664', '0.10223', '0.1953', '-0.05914', '-0.06097', '-0.0954', '-0.416', '0.1941', '-0.1394', '0.2708', '0.2402', '0.343', '-0.0008345', '-0.6396', '0.11395', '-0.0743', '0.1908', '-0.1719', '0.3674', '-0.1081', '0.12335', '-0.5474', '0.1484', '0.0583', '-0.3914', '-0.2272', '-0.02605', '0.1805', '0.432', '-0.4019', '-0.04327', '-0.1904', '-0.11426', '-0.1298', '0.707', '-0.03323', '0.4963', '0.1692', '0.2656', '0.4578', '0.3357', '-0.2522', '0.2598', '0.004112', '0.2197', '0.7188', '0.0816', '0.7817', '-0.1343', '0.5845', '0.287']",,,C538256,,,,
mondo:0011774,autosomal recessive nonsyndromic hearing loss 30,"['DFNB30', 'autosomal recessive nonsyndromic deafness type 30', 'deafness, autosomal recessive 30', 'deafness, autosomal recessive type 30', 'autosomal recessive nonsyndromic deafness caused by mutation in MYO3A', 'autosomal recessive nonsyndromic deafness 30', 'autosomal recessive deafness 30', 'MYO3A autosomal recessive nonsyndromic deafness']",0110489,607101,,C1846784,,,,C564624,,,,
mondo:0011775,"nasopharyngeal carcinoma, susceptibility to, 1","['nasopharyngeal carcinoma caused by mutation in TP53', 'nasopharyngeal carcinoma, susceptibility to, 1', 'NPC', 'TP53 nasopharyngeal carcinoma', 'nasopharyngeal cancer', 'nasopharyngeal carcinoma', 'nasopharyngeal carcinoma, somatic', 'nasopharyngeal carcinoma 1', 'Npca']",,607107,,C1846758,,,,,,,,
mondo:0011776,CINCA syndrome,"['IOMID syndrome', 'chronic neurologic cutaneous and articular syndrome', 'NOMID syndrome', 'CINCA/NOMID', 'CINCA syndrome', 'neonatal-onset multisystem inflammatory disease', 'multisystem inflammatory disease, neonatal-onset', 'infantile onset multisystem inflammatory disease', 'neonatal onset multisystem inflammatory disease', 'NOMID', 'infantile-onset multisystem inflammatory disease', 'chronic infantile neurological cutaneous and articular syndrome', 'IOMID', 'Cryopyrin-associated periodic syndrome 3', 'chronic infantile neurological cutaneous articular syndrome', 'Prieur Griscelli syndrome', 'cryopyrin-associated periodic syndrome 3', 'CINCA', 'Prieur-Griscelli syndrome']",0090029,607115,1451,,"['-0.2979', '0.1652', '-0.01953', '0.347', '0.1004', '-0.207', '0.251', '0.393', '-0.4258', '0.5835', '-0.4224', '0.1096', '-0.316', '0.1523', '-0.4202', '-0.1705', '0.1132', '0.03387', '0.1671', '-0.43', '0.281', '-0.2915', '0.0671', '-0.42', '-0.11005', '0.1335', '-0.1681', '0.2842', '-0.2896', '-0.3281', '0.2935', '0.3262', '0.266', '0.2079', '0.2173', '-0.009445', '-0.2764', '-0.751', '-0.1393', '0.2642', '-0.02733', '-0.6045', '0.5327', '-0.2996', '0.1681', '0.541', '-0.0713', '-0.388', '0.02579', '0.2262', '-0.4377', '0.4895', '0.3328', '-0.3027', '-0.002806', '0.03946', '0.2727', '-0.1642', '-0.3108', '0.10187', '0.0295', '0.603', '-0.753', '0.2123', '-0.1893', '-0.1469', '0.1863', '0.3484', '0.2349', '0.808', '-0.353', '0.381', '0.1655', '-0.394', '-0.10345', '0.6147', '0.359', '0.4026', '0.1862', '-0.4072', '0.3662', '-0.5884', '-0.441', '0.766', '-0.1307', '0.0966', '0.57', '0.8145', '-0.4883', '0.6704', '0.756', '0.1127', '0.3552', '-0.1873', '0.2998', '0.03833', '0.4336', '-0.2091', '0.0946', '-0.2245']",C116380,,,759.89,,,
mondo:0011777,Alzheimer disease 8,"['Alzheimer^s disease 8', 'AD8', 'Alzheimer disease, familial 8', 'Alzheimer disease type 8', 'Alzheimer^s disease type 8', 'Alzheimer disease, familial, 8', 'Ad8', 'Alzheimer disease 8']",0110041,607116,,C1846735,,,,C564622,,,,
mondo:0011778,"multiple epiphyseal dysplasia, Al-Gazali type","['AGBK', 'AL-Gazali-BAKALINOVA syndrome', 'Al-Gazali-Bakalinova syndrome', 'multiple epiphyseal dysplasia-macrocephaly-distinctive facies syndrome', 'macrocephaly with multiple epiphyseal dysplasia and distinctive facies', 'Mmedf']",,607131,166024,,"['-0.4028', '0.05038', '0.4158', '-0.64', '0.1514', '-0.2993', '-0.2925', '0.337', '-0.7427', '-0.1309', '-0.138', '0.1296', '-0.1001', '-0.1167', '-0.10736', '0.5327', '0.195', '-0.10767', '-0.2064', '-0.507', '-0.0698', '0.0634', '0.7305', '-0.1218', '0.0906', '0.1376', '-0.2205', '-0.3552', '0.2605', '-0.353', '0.2324', '-0.152', '0.2886', '0.4387', '0.2717', '-0.0709', '-0.4836', '-0.3691', '-0.4338', '-0.645', '0.0807', '-0.3865', '0.156', '0.0776', '-0.16', '-0.5464', '-0.0798', '0.4805', '0.144', '0.04205', '0.3948', '-0.0961', '0.2556', '0.245', '-0.3333', '-1.048', '-0.1641', '-0.2062', '-0.005535', '0.0967', '0.328', '0.0434', '-0.523', '0.0353', '0.03815', '-0.04938', '0.2053', '0.3652', '-0.02568', '0.4055', '-0.348', '0.2496', '0.164', '-0.1876', '0.05594', '0.331', '0.0382', '0.1018', '-0.5146', '-0.12213', '-0.09564', '0.03464', '-0.1255', '0.4429', '-0.11053', '0.3218', '-0.131', '0.2346', '0.1659', '-0.03662', '-0.1414', '0.2385', '0.4136', '0.02766', '0.6675', '0.3352', '0.54', '-0.2218', '0.404', '0.2201']",,,C564621,,Q77.3,,
mondo:0011779,"laryngeal atresia, encephalocele, and limb deformities","['laryngeal atresia, encephalocele, and limb deformities', 'Lel']",,607132,,C1846721,,,,C564620,,,,
mondo:0011780,specific language impairment 3,"['SLI3', 'specific language impairment quantitative trait locus on chromosome 13', 'specific language impairment 3', 'specific language impairment QTL, 3']",,607134,,C1846719,,,,,,,,
mondo:0011781,spinocerebellar ataxia type 17,"['CPD, late-onset recessive type', 'olivopontocerebellar atrophy type 5', 'spinocerebellar ataxia 17', 'SCA 17', 'OPCA with dementia and extrapyramidal signs', 'SCA17', 'olivopontocerebellar atrophy V', 'cerebelloparenchymal disorder II', 'olivopontocerebellar atrophy 5', 'Huntington disease-like 4', 'spinocerebellar ataxia type 17', 'HDL4', 'CPD2', 'OPCA V']",0050967,607136,98759,C1859299,"['0.00728', '0.0432', '-0.1595', '0.1719', '-0.4019', '-1.038', '0.4155', '0.4434', '-0.6455', '-0.8647', '0.2208', '0.10297', '-0.10486', '-0.02278', '0.922', '-0.3513', '-0.2385', '-0.46', '-0.0445', '-0.701', '-0.2275', '-0.4346', '0.2306', '-0.672', '0.655', '-0.4617', '-0.5293', '0.1821', '-0.2438', '-0.7153', '0.3718', '0.1923', '-0.506', '-0.2173', '0.3633', '-0.0637', '0.08014', '-0.1947', '0.1942', '0.68', '0.5493', '0.1223', '-0.5557', '0.152', '0.745', '-0.4849', '-0.1', '0.3828', '0.1631', '-0.1973', '-0.1681', '-0.0935', '-0.1232', '-0.5713', '-0.02118', '-0.803', '0.429', '0.516', '0.1703', '0.231', '-0.6484', '0.3884', '0.3342', '-0.2524', '-0.2286', '0.3772', '0.1665', '0.58', '-0.7344', '0.4727', '0.736', '0.3674', '-0.1399', '-0.5093', '0.573', '0.507', '0.3474', '-0.0907', '-0.1082', '0.2288', '-0.1647', '-0.9067', '0.5225', '0.513', '-0.1871', '-0.4595', '0.4224', '0.0362', '0.6465', '0.1296', '0.626', '0.1902', '-0.07007', '-0.1755', '0.97', '0.9844', '0.4583', '0.5327', '-0.1711', '-0.1559']",C179861,,C565866,,,,
mondo:0011782,angioid streaks,['angioid streaks'],13401,607140,,C0002982,,,1000805,D000793,,,10066191,
mondo:0011783,ALG12-congenital disorder of glycosylation,"['CDG 1G', 'CDG1G', 'congenital disorder of glycosylation type Ig', 'CDG syndrome type Ig', 'congenital disorder of glycosylation, type Ig', 'CDGIg', 'ALG12-CDG (CDG-Ig)', 'mannosyltransferase 8 deficiency', 'CDG Ig', 'ALG12-congenital disorder of glycosylation', 'congenital disorder of glycosylation type 1g', 'ALG12-CDG', 'CDG-Ig', 'carbohydrate deficient glycoprotein syndrome type Ig']",0080559,607143,79324,C2931001,"['-0.2778', '-0.033', '0.4023', '-0.5347', '0.03262', '-0.2073', '0.02441', '0.478', '-0.5635', '-0.0791', '0.1356', '-0.3945', '-0.153', '0.03333', '-0.368', '0.1615', '0.2238', '0.05692', '-0.5103', '-0.2864', '0.213', '0.0041', '0.2324', '0.00524', '0.4214', '0.03738', '-0.05353', '-0.0554', '0.2532', '-0.3337', '0.2576', '0.1256', '0.598', '0.00949', '-0.1109', '-0.06824', '-0.2832', '-0.09424', '-0.2438', '-0.2056', '0.10913', '-0.218', '-0.1323', '0.269', '-0.1544', '-0.1149', '0.11816', '0.0533', '0.1426', '0.3408', '-0.39', '-0.07556', '0.08453', '-0.0006084', '-0.2783', '-0.1721', '0.0846', '-0.0712', '-0.1189', '0.287', '-0.1288', '0.08716', '0.1636', '0.2003', '0.1139', '-0.02774', '0.0655', '0.1141', '-0.4263', '0.2279', '-0.4556', '0.3362', '0.1787', '0.2363', '0.07526', '0.03882', '0.8223', '-0.04724', '-0.1455', '0.164', '0.036', '-0.1257', '0.2659', '0.3418', '-0.06476', '-0.0313', '-0.04184', '0.3716', '0.3914', '0.1693', '-0.1658', '0.426', '0.01967', '0.06238', '0.506', '0.604', '0.2444', '-0.2056', '0.04184', '0.3936']",C126873,,C535745,271.8,,,
mondo:0011784,Moyamoya disease 2,"['RNF213 Moyamoya disease', 'Moyamoya disease type 2', 'moyamoya disease 2, susceptibility to', 'Moyamoya disease caused by mutation in RNF213', 'MYMY2', 'Moyamoya disease 2']",,607151,,C1846689,,C183312,,C536992,,,,
mondo:0011785,hereditary spastic paraplegia 19,"['SPG19', 'autosomal dominant spastic paraplegia 19', 'spastic paraplegia 19', 'autosomal dominant spastic paraplegia type 19', 'hereditary spastic paraplegia type 19', 'spastic paraplegia 19, autosomal dominant']",0110772,607152,100999,C1846685,,,,C536856,,,,
mondo:0011786,allergic rhinitis,"['Perenial allergic rhinitis', 'seasonal allergic rhinitis', 'allergic rhinitis', 'non-seasonal allergic rhinitis', 'perennial allergic rhinitis', 'pollenosis', 'atopic rhinitis', 'allergic form of rhinitis', 'Alrh']",4481,,,C2607914,"['0.05392', '0.903', '-0.4565', '0.3594', '-0.6313', '-0.511', '0.2803', '0.1506', '-0.1202', '-0.8037', '0.4844', '0.2408', '-0.3257', '0.8364', '-0.91', '-0.136', '-0.5845', '-0.3267', '-0.4973', '-0.141', '0.0472', '0.03836', '0.2494', '0.01091', '0.11926', '-0.2544', '-0.1346', '0.618', '-0.03345', '-0.3425', '0.09906', '0.1175', '-0.444', '0.1886', '-0.3054', '-0.0882', '-0.7305', '0.04337', '-0.4514', '-0.2135', '0.4675', '0.3396', '-0.4407', '-0.623', '0.2043', '-0.01657', '-0.0976', '0.3665', '0.384', '0.9883', '-0.437', '-0.6064', '0.385', '0.2091', '0.05634', '0.0809', '-0.3755', '0.689', '-0.281', '-0.3677', '-0.3591', '0.7686', '-0.3494', '0.0009313', '0.1432', '0.4663', '0.9126', '0.7153', '0.2676', '1.251', '-0.4292', '-0.287', '0.5977', '-0.6006', '-0.2805', '0.7837', '0.699', '0.2399', '0.691', '0.411', '0.12036', '-0.5723', '-0.1608', '0.2893', '0.0934', '-0.261', '0.1652', '0.333', '0.3032', '0.422', '0.2964', '0.3423', '-0.3196', '0.3035', '0.352', '-0.1823', '-0.2615', '-0.891', '-0.6353', '-0.4314']",C79532,0005854,,477.9,,,0003193
mondo:0011787,autosomal recessive limb-girdle muscular dystrophy type 2I,"['LGMD2I', 'muscular dystrophy-dystroglycanopathy limb-girdle FRKP-related', 'FKRP autosomal recessive limb-girdle muscular dystrophy', 'LGMD-FKRP related', 'muscular dystrophy limb-girdle type 2I', 'muscular dystrophy, limb-girdle, type 2I', 'muscular dystrophy-dystroglycanopathy (limb-girdle) type C 5', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in FKRP', 'limb-girdle muscular dystrophy due to FKRP deficiency', 'muscular dystrophy-dystroglycanopathy (limb-girdle), type C, 5', 'limb-girdle muscular dystrophy type 2I', 'muscular dystrophy-dystroglycanopathy, limb-girdle, Frkp-related', 'muscular dystrophy-dystroglycanopathy (Limb-girdle) type C, 5', 'MDDGC5']",0110299,607155,34515,,"['0.135', '-0.375', '-0.789', '-0.344', '0.641', '-1.042', '0.2065', '0.9346', '-1.743', '-0.5786', '-0.0878', '0.5195', '-0.1205', '0.4836', '0.0908', '0.1382', '-0.634', '-0.3672', '-0.694', '-0.5586', '-0.2261', '-0.04608', '0.282', '0.456', '-0.0515', '-0.301', '0.1316', '-0.4084', '0.081', '-0.4482', '0.698', '0.3992', '0.186', '0.1698', '0.143', '-0.1873', '-0.2874', '0.7197', '0.2125', '-0.2343', '-0.1213', '-0.25', '0.01218', '-0.08307', '-0.344', '0.7695', '-0.3794', '0.447', '-0.2428', '0.595', '0.2167', '-0.01067', '-0.06445', '-0.9097', '0.247', '-0.402', '0.4792', '0.315', '-0.2917', '-0.0755', '0.1794', '0.2498', '0.0815', '-0.1698', '0.04294', '-0.1322', '0.01267', '0.4045', '-0.458', '-0.2947', '-0.10406', '0.2812', '-0.1315', '0.2493', '0.798', '0.916', '0.02286', '-0.1914', '0.07043', '-0.012085', '0.1764', '-0.528', '0.04587', '0.1048', '-0.321', '0.4934', '0.02031', '-0.09906', '0.397', '-0.1499', '-0.08203', '-0.727', '0.04947', '0.5454', '0.0743', '0.02304', '0.4941', '-0.7827', '-0.205', '-0.1803']",C126739,,C564612,,,,
mondo:0011788,cloverleaf skull-multiple congenital anomalies syndrome,['multiple congenital anomalies syndrome with cloverleaf skull'],,607161,93267,C1846671,,,,C564611,,,,
mondo:0011789,familial meningioma,"['meningioma, NF2-related, somatic', 'hereditary meningioma', 'meningioma, familial, susceptibility to', 'familial meningioma', 'susceptibility to familial meningioma', 'meningioma, SIS-related', 'hereditary meningioma (disease)', 'meningioma']",4586,607174,,C1333989,"['-0.0184', '0.0688', '-0.02692', '-0.0001514', '0.03342', '-0.0867', '0.021', '0.0966', '-0.0637', '-0.02773', '-0.006104', '-0.010254', '-0.02222', '0.029', '-0.0641', '-0.0511', '-0.02759', '-0.01575', '0.02023', '-0.1334', '0.01012', '-0.04294', '0.0576', '-0.03772', '0.01808', '-0.009636', '0.01653', '-0.03442', '-0.00667', '-0.0387', '0.0921', '-3.6e-07', '0.0973', '0.00485', '-0.00708', '-0.03574', '-0.0358', '-0.03186', '-0.01505', '-0.0714', '0.05377', '-0.06683', '0.0728', '-0.0465', '0.03072', '-0.04886', '-0.0323', '0.03522', '0.01244', '0.02275', '0.0157', '0.02844', '0.02881', '0.03186', '-0.0585', '-0.010635', '0.05386', '-0.0369', '-0.1313', '0.02425', '0.05902', '0.03818', '0.03265', '-0.01025', '-0.00903', '0.0461', '0.0816', '0.06934', '-0.0709', '0.0934', '-0.04346', '0.007107', '0.01418', '-0.04538', '0.04318', '0.03156', '-0.0128', '0.03403', '-0.043', '-0.06113', '0.005264', '0.03363', '-0.0291', '0.02782', '-0.01607', '0.0074', '0.0354', '0.03812', '0.0759', '-0.005447', '0.01888', '0.04987', '-0.0251', '0.01317', '0.1439', '0.01845', '0.08203', '-0.1173', '-0.02267', '0.0125']",C5301,,C537443,,,,
mondo:0011790,Amish lethal microcephaly,"['MCPHA', 'microcephaly, Amish type', 'Amish lethal microcephaly', 'thiamine metabolism dysfunction syndrome 3 (microcephaly type)']",,607196,99742,C1846648,"['-0.08075', '0.3462', '0.2395', '0.1043', '0.3132', '-0.1803', '0.4546', '0.942', '-0.974', '-0.1604', '0.1724', '0.1197', '0.357', '0.6157', '0.478', '-0.1483', '0.5425', '0.4292', '-0.4639', '-0.989', '-0.37', '0.05865', '0.4263', '-0.3044', '0.3901', '-0.0353', '-0.206', '-0.01636', '0.2864', '-0.1184', '-0.01199', '-0.553', '0.4167', '0.1987', '-0.4854', '0.8735', '-0.5347', '-0.3894', '0.1334', '-0.2351', '0.07764', '0.2169', '-0.3955', '-0.75', '0.1722', '-0.309', '0.882', '0.2844', '0.2133', '-0.1759', '0.1387', '-0.681', '-0.0756', '-0.4968', '-0.1231', '0.2886', '-0.6006', '0.529', '-0.2603', '0.1744', '0.2747', '0.5454', '0.0963', '0.2427', '-0.427', '0.0285', '0.7524', '-0.576', '-1.279', '0.2443', '-0.603', '1.049', '0.1879', '-0.7144', '0.006424', '0.4653', '0.2335', '-0.2703', '-0.2515', '0.10925', '-0.3142', '1.031', '-0.1385', '0.62', '0.1809', '-0.2573', '0.3877', '-0.532', '0.8926', '0.3145', '0.1345', '0.2388', '-0.067', '0.1661', '-0.2225', '0.459', '0.756', '-0.4375', '0.6494', '-0.7695']",,,C538247,,,,
mondo:0011792,thyroid dyshormonogenesis 6,"['hypothyroidism, congenital, due to dyshormonogenesis, 6', 'thyroid dyshormonogenesis 6', 'thyroid dyshormonogenesis type 6', 'thyroid hormonogenesis, genetic defect in, 6', 'TDH6', 'familial thyroid dyshormonogenesis caused by mutation in DUOX2', 'DUOX2 familial thyroid dyshormonogenesis']",0112189,607200,,C1846632,,,,C564608,,,,
mondo:0011793,"celiac disease, susceptibility to, 5","['CELIAC5', 'GSES', 'gluten-sensitive enteropathy, susceptibility to, 5', 'celiac disease, susceptibility to, 5']",,607202,,,,,,,,,,
mondo:0011795,anonychia-microcephaly syndrome,"['anonychia, total, with microcephaly', 'anonychia total with microcephaly', 'Teebi-Kaurah syndrome', 'total anonychia with microcephaly', 'total anonychia congenita and microcephaly']",,607214,1094,,,,,,,,,
mondo:0011796,"epilepsy, partial, with pericentral spikes","['PEPS', 'Epps', 'epilepsy, partial, with pericentral spikes']",,607221,,C1846609,,,,C564605,,,,
mondo:0011797,infantile-onset ascending hereditary spastic paralysis,"['IAHSP', 'spastic paralysis, infantile-onset ascending', 'spastic paralysis, infantile onset ascending']",,607225,293168,C2931441,"['0.153', '0.4321', '-0.3064', '-0.2067', '-0.615', '-0.6943', '-0.152', '1.179', '-0.6533', '-0.1898', '-0.3357', '-0.03317', '-0.01596', '0.1301', '0.725', '0.2544', '0.075', '-0.651', '-0.1006', '-0.571', '0.2896', '-0.659', '0.377', '-0.02638', '-0.1655', '0.000663', '-0.0505', '0.1527', '-0.7715', '-0.02188', '0.558', '0.1814', '0.1742', '-0.0344', '-0.1572', '-0.0349', '-0.1416', '-0.2374', '0.2976', '0.5347', '0.06506', '-0.5654', '-0.4463', '0.397', '0.3132', '-0.1335', '-0.2756', '0.1019', '0.2637', '0.4058', '-0.3958', '0.2693', '-0.157', '-0.4211', '0.02057', '-0.2456', '0.4177', '-0.238', '0.1754', '0.3545', '0.1406', '0.1897', '0.2537', '-0.1736', '-0.6187', '0.02983', '0.3757', '0.4294', '-0.358', '0.432', '0.03888', '0.10956', '-0.0195', '-0.1979', '0.794', '0.1738', '-0.4536', '0.1075', '-0.6255', '0.0959', '0.347', '-0.2568', '1.142', '0.723', '-0.2686', '-0.11597', '-0.04675', '0.1608', '0.1534', '0.3364', '0.03613', '-0.605', '-0.4282', '0.4167', '0.4507', '-0.03903', '0.4875', '-0.2786', '0.2263', '0.1794']",,,C537217,343.8,,,
mondo:0011798,"hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration","['harp syndrome', 'hypoprebetalipoproteinemia, acanthocytosis, retinitis pigmentosa, and pallidal degeneration']",,607236,157855,C1846582,,,,C564603,,,,
mondo:0011799,autosomal recessive nonsyndromic hearing loss 33,"['autosomal recessive nonsyndromic deafness type 33', 'deafness, autosomal recessive 33', 'DFNB33', 'autosomal recessive nonsyndromic deafness 33', 'autosomal recessive deafness 33']",0110492,607239,,C1846576,,,,C564602,,,,
mondo:0011800,glioma susceptibility 4,"['glioma susceptibility 4', 'GLM4']",,607248,,C2750944,,,,,,,,
mondo:0011801,"spinocerebellar ataxia, autosomal recessive, with axonal neuropathy 1","['SCAN1', 'spinocerebellar ataxia, autosomal recessive, with axonal neuropathy', 'autosomal recessive spinocerebellar ataxia with axonal neuropathy', 'spinocerebellar ataxia with axonal neuropathy type 1', 'spinocerebellar ataxia with axonal neuropathy', 'spinocerebellar ataxia type 1 with axonal neuropathy', 'spinocerebellar ataxia autosomal recessive with axonal neuropathy']",0090115,607250,94124,C1846574,"['-0.2798', '-0.2532', '0.01859', '-0.02025', '-0.2712', '-0.9824', '0.1632', '0.1224', '-0.7466', '-0.877', '0.232', '0.2712', '-0.2856', '0.1705', '0.3591', '-0.2378', '-0.1476', '-0.1997', '0.10724', '-0.6494', '-0.0218', '-0.3982', '0.0662', '-0.4287', '0.569', '-0.4673', '-0.3035', '0.1962', '-0.154', '-0.948', '0.1768', '0.4912', '-0.4338', '-0.0961', '0.3271', '-0.00812', '-0.3213', '0.2327', '0.3936', '0.4077', '0.399', '0.1299', '-0.4814', '0.4333', '0.3572', '-0.4968', '0.04166', '0.5684', '0.2441', '-0.2349', '-0.04932', '0.2832', '-0.0906', '-0.285', '0.01617', '-0.88', '0.311', '0.416', '0.088', '0.3752', '-0.4714', '0.2249', '0.3484', '-0.0993', '-0.619', '0.4587', '0.18', '0.658', '-0.3147', '0.397', '0.766', '0.6226', '-0.1592', '-0.8535', '0.786', '0.24', '0.2766', '0.386', '0.1844', '0.294', '-0.437', '-0.872', '0.537', '0.956', '-0.1075', '-0.672', '0.1724', '-0.00614', '0.4949', '0.557', '0.467', '0.3616', '0.1565', '-0.0521', '1.084', '1.01', '0.513', '0.66', '-0.3389', '0.1049']",,,C537313,,,,
mondo:0011802,"hypercalciuria, absorptive, 1","['hypercalciuria, absorptive, 1', 'hypercalciuria, absorptive, type 1', 'hypercalciuria, absorptive', 'Hca1']",,607258,,C1846573,,,,C564600,,,,
mondo:0011803,hereditary spastic paraplegia 7,"['SPG7 hereditary spastic paraplegia', 'spastic paraplegia type 7', 'spastic paraplegia 7, autosomal recessive', 'hereditary spastic paraplegia caused by mutation in SPG7', 'hereditary spastic paraplegia paraplegin type', 'hereditary spastic paraplegia type 7', 'autosomal recessive spastic paraplegia 7', 'spastic paraplegia 7', 'SPG7']",0110816,607259,99013,C3711370,"['-0.1682', '0.4417', '0.1982', '-0.02191', '0.1758', '-0.768', '-0.0828', '0.4622', '-0.842', '0.2394', '-0.2299', '0.3123', '-0.3042', '0.1079', '-0.3167', '-0.014854', '0.268', '-0.4314', '0.2483', '-0.432', '-0.1887', '-0.4136', '0.1565', '0.3872', '0.1885', '0.3213', '-0.08026', '0.1466', '-0.1592', '0.01543', '0.264', '-0.02051', '0.4778', '0.5293', '-0.323', '-0.599', '-0.522', '-0.0997', '-0.2834', '-0.0656', '-0.3286', '-0.1947', '0.1934', '0.4358', '-0.1428', '-0.2207', '0.09595', '0.12427', '-0.039', '0.412', '-0.2361', '0.488', '-0.5356', '-0.6816', '0.1602', '-0.683', '0.7393', '-0.4324', '-0.6406', '0.0106', '0.0704', '-0.11163', '0.286', '0.2551', '-0.6763', '0.3494', '0.4683', '0.839', '-0.1576', '0.2367', '-0.1552', '0.6187', '0.1345', '-0.61', '0.9844', '-0.0839', '-0.0836', '-0.2263', '-0.368', '-0.2031', '0.1416', '-0.5356', '0.726', '1.208', '0.02657', '0.2507', '-0.3145', '0.161', '0.1407', '-0.1272', '0.4143', '0.3806', '0.3015', '0.2812', '0.8105', '0.319', '0.729', '0.1416', '-0.2375', '0.1434']",,,C564599,,,,
mondo:0011804,autoimmune lymphoproliferative syndrome type 2B,"['CEDS', 'caspase eight deficiency state', 'autoimmune lymphoproliferative syndrome, type 2B', 'autoimmune lymphoproliferative syndrome, type IIB', 'autoimmune lymphoproliferative syndrome caused by mutation in CASP8', 'caspase-8 deficiency', 'ALPS with recurrent viral infections', 'caspase 8 deficiency', 'ALPS2B', 'autoimmune lymphoproliferative syndrome type IIB', 'autoimmune lymphoproliferative syndrome with recurrent viral infections', 'Ceds', 'CASP8 autoimmune lymphoproliferative syndrome', 'caspase 8 deficiency syndrome']",0110116,607271,275517,,"['0.387', '0.1741', '0.008545', '-0.696', '0.05084', '-0.399', '0.08057', '0.2139', '0.5176', '-0.1995', '-0.07587', '0.1631', '-0.3333', '-0.1708', '-0.1377', '0.3313', '0.01886', '0.1837', '-0.3862', '-0.715', '-0.1841', '-0.266', '0.3096', '-0.4106', '-0.07263', '0.10516', '-0.4792', '0.0577', '0.2168', '-1.014', '0.0985', '0.04544', '0.291', '0.02312', '-0.0944', '-0.665', '-0.566', '-0.3242', '-0.3699', '-0.2556', '-0.06714', '0.1344', '0.5522', '-0.5093', '-0.06555', '-0.3074', '0.1589', '-0.4077', '-0.07855', '0.1012', '-0.3792', '-0.4316', '0.2834', '0.1775', '-0.3228', '-0.02448', '0.06042', '-0.3777', '-0.07086', '0.3835', '0.3035', '0.2081', '0.3145', '0.13', '0.3503', '0.05017', '0.2866', '0.2205', '-0.4614', '0.804', '-0.577', '-0.4697', '-0.2603', '0.1624', '0.3472', '-0.007713', '0.368', '0.04523', '0.0999', '0.2625', '-0.013954', '0.12427', '0.1306', '0.2378', '-0.0255', '-0.1252', '0.642', '0.2603', '0.5884', '0.229', '0.298', '0.6934', '-0.4658', '0.01067', '0.6807', '0.664', '-0.03384', '-0.522', '-0.05823', '-0.5317']",,,,,,,
mondo:0011805,"asthma-related traits, susceptibility to, 1","['AS1', 'PTGDR inherited susceptibility to asthma', 'asthma-related traits, susceptibility to, type 1', 'ASRT1', 'inherited susceptibility to asthma caused by mutation in PTGDR', 'asthma-related traits, susceptibility to, 1', 'asthma, susceptibility to, 1']",,607277,,C1846534,,,,,,,,
mondo:0011806,osteofibrous dysplasia,"['osteofibrous dysplasia', 'OFD', 'ossifying fibroma of long bones', 'tibia, bowing of, with pseudarthrosis and pectus excavatum', 'OSFD', 'osteofibrous dysplasia, susceptibility to', 'cortical fibrous dysplasia', 'osteofibrous dysplasia of bone', 'Kempson-Campanacci lesion']",,609143,488265,C1836723,,C53970,,C563787,,,,
mondo:0011807,"systemic lupus erythematosus with hemolytic anemia, susceptibility to, 1","['SLEH1', 'systemic lupus erythematosus with hemolytic anaemia', 'systemic lupus erythematosus, hemolytic Anemia-related', 'systemic lupus erythematosus with hemolytic anemia, susceptibility to, 1', 'systemic lupus erythematosus with hemolytic anemia']",,607279,,,,,,,,,,
mondo:0011808,cataract 27,"['Ccnp', 'cataract 27, nuclear progressive', 'cataract 27 nuclear progressive', 'CTRCT27', 'cataract type 27', 'cataract 27']",0110233,607304,,C1846520,,,,C564596,,,,
mondo:0011810,horizontal gaze palsy with progressive scoliosis,"['gaze palsy, familial horizontal, with progressive scoliosis', 'progressive external ophthalmoplegia and scoliosis', 'HGPPS', 'gaze palsy, horizontal, with progressive scoliosis', 'ophthalmoplegia, progressive external, and scoliosis']",,,2744,C1846496,"['0.02956', '0.2837', '0.2212', '-0.3074', '0.3518', '-1.113', '0.53', '0.5835', '-1.203', '-0.813', '0.711', '-0.03683', '-0.2966', '0.8984', '-0.1758', '-0.0903', '0.2122', '-0.825', '-0.483', '-0.2769', '0.0855', '0.05054', '0.01005', '0.09357', '-0.1901', '-0.15', '0.02893', '0.1931', '-0.162', '0.5083', '0.2473', '0.1705', '0.3562', '0.0813', '-0.367', '0.08136', '-0.8755', '-0.7607', '-0.0728', '-0.0686', '0.2311', '0.2157', '-0.5483', '0.08997', '0.2756', '0.431', '-0.2264', '0.3206', '-0.1295', '0.3596', '0.3882', '0.0639', '0.4106', '-0.5977', '0.03815', '-0.4102', '-0.5215', '0.3027', '-0.408', '-0.1431', '0.4263', '0.05872', '0.153', '0.506', '-0.3936', '-0.043', '0.10077', '1.094', '0.0968', '0.266', '0.6343', '0.0182', '0.2834', '-0.4514', '-0.1906', '0.63', '0.0393', '0.2517', '-0.1964', '-0.2444', '0.03473', '-0.3733', '-0.1732', '0.1207', '-0.1708', '-0.6235', '0.08496', '-0.2942', '-0.136', '0.4014', '-0.09', '-0.2754', '-0.02943', '0.518', '0.8496', '0.272', '0.313', '0.4417', '0.2786', '0.09973']",,,C564593,737.43,H49.4,,
mondo:0011811,autosomal recessive cerebellar ataxia-saccadic intrusion syndrome,"['spinocerebellar ataxia with saccadic Intrusions', 'spinocerebellar ataxia 24', 'spinocerebellar ataxia 24, formerly', 'spinocerebellar ataxia 24 (formerly)', 'spinocerebellar ataxia autosomal recessive 4', 'SCASI', 'spinocerebellar ataxia, autosomal recessive 4', 'SCAR4']",0111611,607317,95434,C1846492,"['-0.2515', '-0.1032', '0.1143', '-0.0384', '0.02419', '-0.659', '0.1558', '-0.05768', '-0.7183', '-0.6807', '0.33', '0.4714', '-0.1603', '0.293', '0.37', '-0.257', '-0.05756', '-0.3281', '0.2084', '-0.937', '0.0315', '-0.2473', '0.001448', '-0.4382', '0.7134', '-0.3315', '-0.01949', '0.1197', '-0.0556', '-0.53', '0.03903', '0.5', '-0.4675', '-0.06836', '0.2754', '0.12354', '-0.3706', '-0.004993', '0.5366', '0.1644', '0.236', '0.2234', '-0.2437', '0.5757', '0.3303', '-0.571', '0.1186', '0.523', '0.3035', '0.1266', '-0.1472', '0.255', '-0.1788', '-0.318', '0.1096', '-0.79', '0.3691', '0.3906', '-0.1677', '0.5933', '-0.457', '0.3357', '0.255', '-0.2725', '-0.3442', '0.6436', '0.424', '0.4797', '-0.5273', '0.6313', '1.067', '0.6763', '-0.1299', '-0.8022', '0.74', '0.1914', '0.07526', '0.3262', '0.392', '0.2174', '-0.5273', '-0.936', '0.4185', '0.876', '-0.2996', '-0.6675', '0.1857', '-0.1315', '0.2365', '0.549', '0.3154', '0.10803', '0.0699', '-0.04822', '0.97', '1.139', '0.5', '0.1709', '-0.4553', '0.0802']",,,C537310,,,,
mondo:0011812,Duane-radial ray syndrome,"['Duane anomaly with radial abnormalities and deafness', 'Okihiro syndrome', 'Duane-radial ray syndrome', 'acrorenocular syndrome', 'acro-renal-ocular syndrome', 'DRRS', 'DR syndrome', 'Duane anomaly with radial ray abnormalities and deafness']",0060747,607323,959,CN206803,"['0.1401', '-0.065', '0.563', '-0.2201', '0.1884', '-0.2094', '0.0867', '-0.0009327', '-0.1819', '-0.6055', '-0.05902', '-0.5317', '-0.3438', '0.1724', '-0.3916', '-0.4277', '0.06757', '-0.4526', '0.301', '-0.4436', '0.0805', '0.1399', '0.2827', '-0.139', '0.3652', '0.411', '-0.557', '-0.16', '0.667', '-0.331', '0.0973', '0.12476', '0.5435', '0.3333', '0.364', '-0.649', '-0.2362', '0.02597', '-0.5767', '-0.2869', '0.06018', '-0.1161', '0.5273', '-0.6772', '0.6357', '-0.6035', '0.1766', '0.6724', '0.1741', '0.192', '-0.202', '0.508', '-0.10834', '-0.639', '-0.555', '-0.2211', '0.4636', '0.2727', '-0.6504', '0.203', '0.3464', '-0.00423', '-0.1562', '0.2517', '-0.2686', '-0.05945', '0.102', '0.2803', '-0.2886', '0.3657', '-0.4536', '0.4163', '0.564', '-0.451', '0.4668', '-0.02223', '0.1431', '-0.3203', '-0.67', '-0.3445', '0.2754', '-0.11584', '0.4268', '0.6416', '-0.2815', '-0.2339', '0.201', '0.385', '-0.2272', '0.005695', '-0.05933', '0.2854', '0.36', '0.1633', '0.7397', '-0.3723', '0.8022', '-0.3118', '0.1256', '0.772']",,,,759.89,,,
mondo:0011813,"polydactyly, postaxial, type A3","['PAPA3', 'postaxial polydactyly, type A3', 'polydactyly, postaxial, type A3', 'Papa3']",,607324,,C1846452,,,,C564590,,,,
mondo:0011814,Smith-McCort dysplasia 1,"['DYM Smith-McCort dysplasia', 'Smith-McCort dysplasia caused by mutation in DYM', 'SMITH-McCort dysplasia 1', 'Smith-McCort dysplasia', 'SMC', 'Smith-McCort dysplasia type 1', 'Smc1', 'Smith-McCort dysplasia 1']",0081270,607326,,C3888088,,,,,,,,
mondo:0011815,"hypertension, essential, susceptibility to, 3","['hypertension, essential, susceptibility to, type 3', 'hypertension, essential, susceptibility to, 3', 'Hyt3']",,607329,,C1846430,,,,,,,,
mondo:0011816,lathosterolosis,"['Sc5D deficiency', 'lathosterolosis', 'sterol C5-desaturase deficiency']",,607330,46059,C1846421,"['-0.366', '-0.225', '0.1777', '-0.05136', '0.1603', '-0.6445', '-0.4998', '1.02', '-0.2161', '-0.747', '-0.6055', '-0.3972', '0.339', '0.375', '-0.629', '-0.538', '0.3762', '-0.4028', '-0.1403', '-0.2847', '0.1465', '-0.2874', '0.1691', '-0.2476', '0.02455', '-0.1252', '-0.3716', '0.6865', '0.178', '-0.3745', '0.4487', '0.4275', '0.3901', '-0.2051', '-0.1382', '-0.566', '0.4993', '-0.202', '0.01182', '0.02818', '0.009865', '-0.3232', '0.3904', '0.2615', '-0.2815', '-0.3645', '0.2534', '-0.426', '-0.73', '-0.09406', '-0.548', '0.2375', '-0.3005', '0.0333', '-0.1903', '-1.027', '0.2976', '-0.2211', '-0.1486', '0.2607', '-0.02718', '-0.0636', '0.2435', '0.03284', '0.04514', '-0.0685', '0.06107', '0.418', '-0.2974', '-0.24', '-0.557', '0.2595', '0.11096', '0.567', '0.2478', '0.0233', '-0.418', '-0.244', '-0.3918', '0.3362', '-0.2269', '0.456', '0.1826', '0.3682', '0.1616', '0.3635', '0.03616', '0.08295', '0.2573', '0.01249', '-0.03265', '0.648', '-0.374', '0.2167', '0.574', '0.336', '-0.0732', '-0.1545', '0.5596', '0.4219']",,,C537880,,,,
mondo:0011817,"coronary heart disease, susceptibility to, 1","['coronary heart disease, susceptibility to', 'coronary heart disease, susceptibility to, type 1', 'Chds1', 'coronary artery disease caused by mutation in CX3CR1', 'coronary heart disease, susceptibility to, 1', 'CX3CR1 coronary artery disease', 'coronary artery disease, resistance to']",,607339,,C1846418,,,,,,,,
mondo:0011818,isolated focal cortical dysplasia type II,"['cortical dysplasia of Taylor with balloon cells', 'FCD 2B', 'cortical dysplasia of Taylor without balloon cells', 'FCD type II', 'cortical dysplasia of Taylor', 'focal cortical dysplasia type 2', 'FCORD2', 'focal cortical dysplasia, type 2', 'Fcd2', 'focal cortical dysplasia of Taylor, type 2A', 'focal cortical dysplasia of Taylor, type 2B', 'focal cortical dysplasia, type II, somatic', 'focal cortical dysplasia type II', 'focal cortical dysplasia, type 2A', 'cortical dysplasia, Taylor type', 'isolated focal cortical dysplasia type 2', 'focal cortical dysplasia of Taylor', 'focal cortical dysplasia, type 2B', 'FCDT', 'focal cortical dysplasia, type II', 'CDT', 'FCD 2A', 'cortical dysplasia of Taylor, dysplasia only']",,607341,268994,,"['-0.05865', '0.2637', '-0.06274', '-0.171', '0.0891', '0.1559', '0.2188', '0.1092', '-0.2576', '0.005634', '-0.383', '-0.2832', '-0.2089', '-0.1786', '-0.04907', '-0.01389', '-0.04633', '-0.324', '-0.09515', '-0.3157', '0.00887', '-0.04263', '0.4548', '0.05072', '0.11444', '-0.0441', '-0.2166', '-0.1735', '-0.03107', '0.2247', '0.10205', '-0.2042', '0.327', '0.04675', '0.3206', '0.2585', '-0.1655', '-0.1365', '0.01151', '-0.4917', '0.12036', '-0.3794', '-0.061', '0.0403', '-0.08777', '-0.1434', '-0.1863', '0.1041', '-0.013275', '-0.01161', '0.4675', '-0.05603', '0.08246', '0.11115', '-0.3345', '0.0663', '0.2145', '-0.1427', '-0.2013', '0.177', '0.1278', '-0.0681', '0.0759', '-0.03366', '-0.10114', '0.0965', '0.5127', '0.0249', '-0.2666', '0.1952', '0.0788', '0.2524', '0.1866', '-0.01788', '-0.1572', '0.1475', '0.1642', '0.04608', '-0.2617', '-0.2357', '-0.1963', '0.25', '-0.11035', '-0.013336', '-0.08875', '-0.3083', '0.0952', '0.4363', '0.3743', '0.0671', '-0.0111', '0.3728', '0.0409', '0.08545', '0.4348', '0.05884', '0.4778', '-0.1946', '0.2722', '0.2205']",,,C537067,,,,
mondo:0011819,spinocerebellar ataxia type 19/22,"['spinocerebellar ataxia 19', 'spinocerebellar ataxia 22', 'SCA19/22', 'spinocerebellar ataxia type 19', 'spinocerebellar ataxia 19 and 22', 'SCA19']",0050970,607346,98772,,"['-0.1407', '-0.135', '-0.2323', '0.1959', '-0.1902', '-0.726', '0.4353', '0.252', '-0.8027', '-1.145', '0.3564', '0.1318', '-0.2625', '0.1862', '0.8423', '-0.381', '-0.0984', '-0.4878', '0.1489', '-0.9526', '-0.3054', '-0.3135', '0.143', '-0.4446', '0.7075', '-0.439', '-0.35', '0.1747', '-0.2212', '-0.9272', '0.2715', '0.464', '-0.5723', '-0.3928', '0.4507', '-0.04776', '-0.05798', '0.2369', '0.3782', '0.459', '0.463', '0.1302', '-0.522', '0.2267', '0.6846', '-0.757', '0.068', '0.4204', '0.1406', '-0.04465', '0.0332', '0.092', '-0.1349', '-0.4446', '0.07983', '-0.7495', '0.2676', '0.3752', '0.1151', '0.3037', '-0.6597', '0.327', '0.1862', '-0.2474', '-0.3784', '0.595', '0.1771', '0.793', '-0.6416', '0.2534', '0.8335', '0.4185', '0.013275', '-0.838', '0.8135', '0.3362', '0.4133', '0.3481', '0.04462', '0.5684', '-0.3262', '-0.964', '0.3845', '0.722', '-0.0955', '-0.6855', '0.0622', '0.01913', '0.679', '0.3223', '0.532', '0.4795', '-0.07135', '-0.2451', '0.926', '0.847', '0.3315', '0.4854', '-0.2551', '0.1039']",C163756,,C542540,,,,
mondo:0011820,"scoliosis, isolated, susceptibility to, 2","['IS2', 'scoliosis, isolated, susceptibility to, 2', 'scoliosis, idiopathic 2']",,607354,,,,,,,,,,
mondo:0011821,"Meckel syndrome, type 3","['Meckel syndrome, type 3', 'Meckel-Gruber syndrome, type 3', 'MKS3', 'Meckel syndrome 3', 'TMEM67 Meckel syndrome', 'Meckel syndrome type 3', 'Meckel syndrome caused by mutation in TMEM67']",0070117,607361,,C1846357,,,,C536132,,,,
mondo:0011822,Bartter disease type 3,"['adult Bartter syndrome', 'classic Bartter syndrome', 'Bartter syndrome classic', 'Bartter syndrome type III', 'Bartter syndrome, type 3, with hypocalciuria', 'Bartter syndrome, type 3', 'Bartter syndrome, classic', 'BARTS3', 'Bartter syndrome type 3']",0110144,607364,93605,C1846343,"['-0.05734', '-0.1327', '-0.652', '-0.1829', '-0.473', '-0.1848', '0.1357', '0.4795', '-0.3335', '-0.05234', '0.04767', '-0.0626', '0.4397', '0.2632', '-0.4463', '0.03543', '-0.1273', '0.3118', '0.714', '-0.681', '-0.1936', '-0.4941', '0.6074', '0.003666', '0.3774', '0.5093', '0.01286', '-0.1192', '0.006355', '-0.0873', '0.2043', '-0.005733', '0.4824', '0.5576', '-0.1608', '-0.2268', '-0.1877', '0.1311', '-0.3372', '-0.3862', '-0.1415', '-0.4424', '0.3613', '-0.4531', '0.4744', '-0.2341', '-0.3071', '0.3389', '-0.044', '0.2866', '-0.1324', '-0.2957', '0.2467', '-0.8696', '-0.3276', '0.0355', '-0.1046', '-0.3542', '0.3213', '0.3975', '-0.3865', '0.211', '0.09033', '-0.7017', '-0.03693', '-0.445', '0.1449', '0.4915', '-0.3674', '0.5293', '-0.4775', '0.183', '0.484', '0.1487', '0.4202', '0.3538', '-0.3167', '-0.4211', '0.0501', '0.03885', '-0.1124', '0.2903', '-0.762', '0.0874', '-0.0828', '0.867', '0.4763', '-0.1017', '1.114', '-0.265', '0.794', '-0.02304', '0.2114', '0.1937', '0.3926', '0.4158', '0.1459', '-0.3743', '-0.1954', '0.521']",,,,,,,
mondo:0011823,developmental malformations-deafness-dystonia syndrome,"['dystonia, juvenile-onset', 'DJO', 'juvenile-onset dystonia']",,607371,79107,C1846331,"['0.8027', '0.207', '0.1633', '-0.493', '-0.1142', '-1.1', '0.5444', '0.0647', '-0.654', '-0.093', '0.857', '0.4138', '-0.1892', '0.283', '0.581', '0.562', '0.05725', '-0.558', '-0.9136', '-0.9873', '-0.2238', '-0.1898', '-0.02516', '-0.295', '-0.2191', '-0.03653', '-0.2369', '0.0736', '0.1361', '0.1057', '0.4846', '0.4553', '1.11', '-0.1597', '0.749', '-0.011894', '0.8364', '-0.1837', '0.2646', '-0.4785', '0.4658', '0.2047', '-0.3113', '0.02757', '0.6216', '-0.1746', '-0.276', '0.2542', '0.447', '0.2383', '0.03687', '0.05273', '0.7974', '-0.0471', '0.424', '-0.2394', '0.153', '0.655', '0.0634', '-0.1814', '-0.7583', '-0.709', '-0.3252', '-0.6616', '-1.176', '0.618', '0.2075', '0.3303', '-0.488', '0.2908', '-0.1356', '0.005512', '0.0708', '-0.303', '0.2458', '0.2435', '0.907', '-0.01303', '0.0251', '-0.1041', '-0.0973', '0.08875', '0.2827', '0.63', '0.888', '-0.0466', '-0.007256', '0.542', '1.51', '0.1562', '0.3442', '0.301', '0.64', '0.1797', '1.114', '-0.184', '-0.4229', '-0.02055', '0.4595', '-0.402']",,,C537704,,,,
mondo:0011824,"autism, susceptibility to, 8","['autism susceptibility 8, isolated cases', 'autism, susceptibility to, 8', 'AUTS8', 'AUTS2', 'AUTS2, formerly']",,607373,,,,,,,,,,
mondo:0011825,"streptococcus, group A, severity of infection by","['streptococcus, group A, severity of infection by']",,607395,,,,,,,,,,
mondo:0011826,glucocorticoid deficiency 2,"['MRAP familial glucocorticoid deficiency', 'familial glucocorticoid deficiency caused by mutation in MRAP', 'familial glucocorticoid deficiency 2', 'glucocorticoid deficiency type 2', 'GCCD2', 'glucocorticoid deficiency 2']",,607398,,C1846284,,C123728,,C564577,,,,
mondo:0011827,patent ductus arteriosus,"['PDA', 'patent ductus arteriosus', 'patent ductus arteriosus familial (type)', 'ductus arteriosus, patent', 'patent ductus botalli', 'persistent patency of the arterial duct', 'patency of the ductus arteriosus']",13832,,706,,,C84492,,D004374,747.0,Q25.0,,
mondo:0011828,"intellectual disability, autosomal recessive 2","['autosomal recessive non-syndromic intellectual disability caused by mutation in CRBN', 'mental retardation, autosomal recessive 2A', 'MRT2', 'intellectual disability, autosomal recessive type 2', 'intellectual disability, autosomal recessive 2', 'CRBN autosomal recessive non-syndromic intellectual disability', 'mental retardation, autosomal recessive type 2', 'mental retardation, autosomal recessive 2', 'intellectual disability, autosomal recessive 2A']",0081178,607417,,C1843942,,,,C564404,,,,
mondo:0011829,"coenzyme Q10 deficiency, primary, 1","['coenzyme Q10 deficiency, primary, type 1', 'COQ10D1', 'Coq10 deficiency, primary, 1', 'COQ2 coenzyme Q10 deficiency', 'coenzyme Q10 deficiency, primary, 1', 'coenzyme Q deficiency 1', 'coenzyme Q10 deficiency caused by mutation in COQ2', 'ubiquinone deficiency 1', 'CoQ deficiency 1']",0070238,607426,,C3551954,,,,,,,,
mondo:0011830,lissencephaly due to LIS1 mutation,"['lissencephaly sequence, isolated', 'PAFAH1B1-related lissencephaly', 'subcortical band heterotopia', 'lissencephaly 1', 'LIS1', 'lissencephaly, classic', 'subcortical laminar heterotopia']",0112237,607432,99796,CN228917,"['-0.3733', '0.2118', '0.3098', '-0.245', '0.286', '-0.03647', '-0.00924', '0.1766', '-0.4934', '-0.01572', '-0.5664', '-0.2032', '0.1344', '-0.02618', '0.319', '-0.1376', '-0.1448', '-0.3137', '-0.0942', '-0.4985', '0.0714', '0.0894', '0.3828', '-0.2319', '0.2996', '-0.168', '-0.00523', '0.25', '-0.1794', '0.0355', '0.1354', '0.06122', '0.4968', '0.179', '0.003769', '0.231', '-0.2346', '-0.0721', '-0.03616', '-0.3562', '0.4128', '-0.3066', '0.0588', '-0.03604', '-0.07513', '-0.3228', '0.1256', '-0.0794', '-0.03093', '0.05878', '0.1122', '0.2263', '-0.4302', '-0.1344', '-0.1114', '0.02957', '0.08026', '-0.0655', '-0.2228', '0.1428', '0.12354', '0.0285', '0.0705', '0.111', '0.03647', '0.3264', '0.363', '0.3071', '-0.4504', '0.127', '-0.1002', '0.251', '0.006283', '0.0008373', '-0.07275', '-0.1448', '0.602', '-0.1311', '-0.2281', '-0.4626', '-0.1786', '-0.0233', '-0.2573', '0.3901', '0.229', '-0.11725', '-0.07874', '0.2515', '0.3198', '-0.014786', '0.305', '0.538', '-0.0535', '0.1045', '0.2664', '-0.03668', '0.6426', '-0.1659', '0.5615', '0.2362']",,,,,,,
mondo:0011831,arrhythmogenic right ventricular dysplasia 8,"['DSP arrhythmogenic right ventricular cardiomyopathy', 'arrhythmogenic right ventricular cardiomyopathy 8', 'familial arrhythmogenic right ventricular dysplasia 8', 'arrhythmogenic right ventricular dysplasia, familial, 8', 'ARVC8', 'arrhythmogenic right ventricular dysplasia type 8', 'arrhythmogenic right ventricular cardiomyopathy caused by mutation in DSP', 'arrhythmogenic right ventricular dysplasia, familial, type 8', 'ARVD8']",0110076,607450,,C1843896,,,,C564400,,,,
mondo:0011832,autosomal dominant nonsyndromic hearing loss 44,"['deafness, autosomal dominant type 44', 'autosomal dominant nonsyndromic deafness 44', 'autosomal dominant nonsyndromic deafness type 44', 'CCDC50 autosomal dominant nonsyndromic deafness', 'DFNA44', 'deafness, autosomal dominant 44', 'autosomal dominant nonsyndromic deafness caused by mutation in CCDC50', 'autosomal dominant deafness 44']",0110569,607453,,C1843895,,,,C564399,,,,
mondo:0011833,spinocerebellar ataxia type 21,"['spinocerebellar ataxia type 21', 'SCA21', 'spinocerebellar ataxia 21']",0050972,607454,98773,C4305144,"['-0.0942', '-0.1805', '-0.1783', '-0.0381', '-0.2854', '-0.8716', '0.385', '0.2957', '-0.4807', '-0.9043', '0.135', '0.2256', '-0.1874', '0.05383', '0.588', '-0.25', '-0.01217', '-0.2927', '0.0669', '-1.043', '-0.1774', '-0.302', '0.3171', '-0.5283', '0.4355', '-0.515', '-0.427', '0.2294', '-0.1223', '-0.671', '0.0008073', '0.397', '-0.4324', '-0.3638', '0.2231', '0.0887', '-0.164', '0.04767', '0.5', '0.5273', '0.3506', '0.3308', '-0.4312', '0.4026', '0.672', '-0.6113', '0.1866', '0.3967', '0.1353', '0.03214', '-0.0877', '0.272', '-0.1415', '-0.378', '-0.0813', '-0.668', '0.277', '0.541', '0.1627', '0.4243', '-0.8115', '0.353', '0.2242', '-0.266', '-0.4153', '0.5874', '0.379', '0.6875', '-0.6284', '0.3984', '0.8735', '0.4692', '-0.07446', '-0.8257', '0.593', '0.3872', '0.1593', '0.2496', '0.1194', '0.507', '-0.3665', '-0.839', '0.433', '0.6245', '-0.214', '-0.751', '0.3267', '0.01136', '0.6787', '0.4714', '0.6274', '0.4026', '-0.06915', '-0.0203', '1.031', '1.024', '0.4053', '0.498', '-0.189', '-0.10504']",,,C537200,,,,
mondo:0011834,spinocerebellar ataxia type 18,"['SMNA', 'sensorimotor neuropathy with ataxia autosomal dominant', 'sensorimotor neuropathy with ataxia, autosomal dominant', 'SCA18', 'spinocerebellar ataxia 18']",0050969,607458,98771,C4304848,,,,C537197,,,,
mondo:0011835,"sensory ataxic neuropathy, dysarthria, and ophthalmoparesis","['PRICKLE2 progressive myoclonic epilepsy', 'sensory ataxic neuropathy-dysarthria-ophthalmoparesis syndrome', 'sensory ataxic neuropathy, dysarthria, and ophthalmoparesis', 'mitochondrial recessive ataxia syndrome (includes SANDO and SCAE)', 'epilepsy, progressive myoclonic, 5, formerly', 'progressive myoclonus epilepsy type 5', 'sensory ataxic neuropathy with mitochondrial DNA deletions, autosomal recessive', 'epilepsy, progressive myoclonic, with sensory ataxic neuropathy', 'SANDO', 'PME type 5', 'progressive myoclonic epilepsy caused by mutation in PRICKLE2', 'EPM5', 'epilepsy, progressive myoclonic, type 5', 'spinocerebellar ataxia with epilepsy', 'epilepsy, progressive myoclonic, 5']",0111276,613832,70595,CN226157,"['0.4097', '0.3406', '0.04407', '-0.05298', '-1.144', '-0.503', '0.5103', '0.2046', '-1.0205', '-0.2236', '0.853', '0.02661', '-0.1309', '-0.0634', '0.4683', '-0.3105', '0.2125', '-0.1305', '-0.3665', '-0.594', '0.1279', '0.3752', '-0.74', '0.002222', '0.06537', '-0.3425', '-0.2374', '-0.275', '0.2996', '-0.1295', '-0.1175', '0.433', '0.733', '0.04086', '0.3684', '-0.01648', '-0.01057', '0.01358', '-0.2208', '-0.5615', '0.1027', '-0.2588', '-0.7935', '0.3523', '0.4421', '-0.256', '0.1726', '0.326', '0.03568', '-0.010315', '-0.3838', '0.62', '0.02765', '-0.6514', '0.2079', '0.2473', '-0.2566', '0.066', '-0.1068', '0.1531', '-0.04617', '-0.04663', '0.1746', '0.03693', '-0.798', '0.0727', '0.2378', '0.4348', '-0.9067', '0.11005', '-0.3894', '-0.0608', '-0.0984', '-0.7036', '0.1203', '0.5044', '0.4653', '0.6636', '-0.3557', '-0.4084', '0.1428', '-0.1522', '0.1459', '0.3245', '0.1885', '-0.01415', '-0.2437', '0.0467', '0.812', '0.6523', '0.4277', '-0.1356', '0.4917', '0.7227', '0.6714', '0.648', '-0.03888', '0.5767', '-0.05728', '0.173']",,,,,,,
mondo:0011836,thyroid Hurthle cell carcinoma,"['Hurthle cell thyroid cancer', 'oncocytic carcinoma of the thyroid', 'thyroid carcinoma, Hurthle cell', 'Hurthle cell thyroid neoplasia', 'follicular thyroid cancer, Hurthle cell type', 'thyroid cancer, follicular, Hurthle cell type', 'thyroid cancer, Hurthle cell']",8161,607464,,,,C4946,,C536913,,,,
mondo:0011837,"vitamin K-dependent clotting factors, combined deficiency of, type 2","['congenital vitamin K-dependent coagulation factors combined deficiency caused by mutation in VKORC1', 'vitamin K-dependent clotting factors, combined deficiency of, 2', 'VKCFD2', 'VKORC1 congenital vitamin K-dependent coagulation factors combined deficiency']",0112174,607473,,C1843832,,,,C564393,,,,
mondo:0011838,Bothnia retinal dystrophy,"['Västerbotten dystrophy', 'VC$sterbotten dystrophy', 'Bothnia retinal dystrophy', 'Vasterbotten dystrophy']",0050683,607475,85128,C1843816,"['-0.6665', '-0.261', '-0.353', '-0.3245', '0.1302', '-0.8315', '-0.2615', '0.765', '-0.4348', '-0.2343', '-0.0784', '0.0679', '-0.4524', '-0.1465', '0.1638', '-0.5127', '0.0921', '-0.4797', '0.01903', '-0.3872', '0.1512', '-0.12244', '0.2448', '0.1824', '-0.2343', '0.4902', '-0.594', '-0.1687', '-0.311', '0.2688', '0.3762', '-0.731', '-0.0877', '0.4392', '0.1248', '0.606', '-0.3713', '-0.1209', '-0.2362', '-0.4768', '0.4104', '-0.3086', '0.1853', '-0.1048', '-0.457', '0.3506', '0.3882', '-0.1603', '0.08344', '0.2266', '0.566', '0.06027', '0.3394', '-0.1719', '0.4392', '-0.5547', '1.308', '-0.3567', '-0.2651', '0.502', '0.3325', '0.2905', '0.3447', '-0.08606', '0.03055', '0.01955', '0.521', '0.6094', '-0.398', '0.6763', '-0.07245', '-0.0797', '0.03802', '0.07196', '0.1772', '-0.3647', '-0.1436', '-0.0414', '-0.2058', '-0.10376', '0.164', '-0.3442', '-0.06433', '0.893', '-0.556', '-0.3499', '-0.09515', '0.06137', '0.6206', '-0.2489', '-0.1654', '0.1432', '0.10504', '0.2642', '0.2133', '-0.08264', '0.658', '-0.2866', '-0.1763', '-0.002235']",,,C564392,,H35.5,,
mondo:0011839,Newfoundland cone-rod dystrophy,"['RLBP1 cone-rod dystrophy', 'NFRCD', 'Newfoundland ROD-cone dystrophy', 'cone-rod dystrophy caused by mutation in RLBP1']",0111015,607476,,C1843815,,,,C564391,,,,
mondo:0011840,dilated cardiomyopathy 1M,"['cardiomyopathy, dilated, type 1M', 'CSRP3 familial isolated dilated cardiomyopathy', 'familial isolated dilated cardiomyopathy caused by mutation in CSRP3', 'CMD1M', 'dilated cardiomyopathy type 1M', 'cardiomyopathy, dilated, 1M']",0110449,607482,,C1843808,,,,C564390,,,,
mondo:0011841,biotin-responsive basal ganglia disease,"['biotin-thiamine-responsive basal ganglia disease', 'BBGD', 'thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive encephalopathy type 2)', 'thiamine-responsive encephalopathy', 'basal ganglia disease, biotin-responsive', 'thiamine metabolism dysfunction syndrome 2 (biotin- or thiamine-responsive type)', 'THMD2', 'encephalopathy, thiamine-responsive', 'BTBGD']",0050659,607483,65284,C1843807,"['-0.1733', '0.2281', '-0.4048', '0.2126', '-0.333', '-0.4302', '-0.11224', '0.2223', '-0.1667', '0.1515', '-0.3745', '-0.3157', '-0.12244', '-0.1586', '0.11835', '0.001595', '-0.11273', '-0.3308', '-0.1874', '-0.455', '-0.1238', '-0.1815', '0.02731', '0.03964', '0.281', '-0.08606', '0.0792', '0.001955', '-0.0918', '-0.1936', '0.0705', '0.09814', '0.1577', '0.302', '-0.326', '0.1055', '-0.05054', '-0.3225', '-0.1184', '0.1792', '0.10803', '-0.3357', '0.35', '-0.01692', '0.13', '-0.2225', '-0.03754', '-0.228', '-0.3762', '-0.1332', '0.069', '0.07654', '0.1654', '0.0414', '0.2957', '-0.1611', '0.4062', '0.2219', '-0.336', '0.3376', '0.00635', '0.0662', '0.4675', '-0.49', '-0.2883', '0.215', '0.4219', '0.4258', '-0.489', '0.4246', '-0.01752', '0.2812', '-0.2588', '-0.2014', '-0.03662', '0.2021', '0.2084', '-0.1656', '0.1375', '0.125', '0.1606', '0.064', '-0.1876', '0.4514', '0.2854', '0.09125', '-0.1373', '0.2273', '0.2369', '0.3596', '0.2185', '0.3115', '-0.007603', '-0.08374', '0.2224', '0.5', '0.3264', '-0.4045', '0.008255', '0.2142']",,,C537658,333.99,,,
mondo:0011842,GRN-related frontotemporal lobar degeneration with Tdp43 inclusions,"['FTLD-TDP, GRN-related', 'frontotemporal dementia, ubiquitin-positive', 'frontotemporal lobar degeneration with ubiquitin-positive inclusions', 'frontotemporal lobar degeneration with TDP43 inclusions, GRN-related', 'dementia, hereditary dysphasic disinhibition', 'frontotemporal dementia with TDP43 inclusions, GRN-related', 'aphasia, primary progressive']",0060672,607485,,,"['-0.02097', '0.02435', '0.00318', '-0.01625', '0.01209', '-0.03583', '0.004875', '0.03128', '-0.02841', '-0.01761', '-0.01663', '-0.00879', '-0.002453', '-0.01152', '0.00844', '-0.04556', '-0.01005', '-0.01714', '-0.01869', '-0.0651', '0.01141', '-0.013756', '0.01994', '-0.0066', '0.02103', '-0.00466', '0.0007453', '-0.005802', '-0.01528', '-0.01566', '0.03174', '-0.0124', '0.03093', '0.008766', '0.0365', '-0.002369', '-0.01582', '-8.1e-06', '-0.01909', '-0.0578', '0.02376', '-0.04736', '0.0086', '-0.01471', '0.0004373', '-0.0263', '0.004627', '0.0316', '0.014145', '0.001638', '0.004124', '0.00955', '-0.004345', '0.0108', '-0.005493', '-0.01923', '0.035', '-0.01068', '-0.0397', '-0.0007772', '0.02138', '0.02094', '0.001404', '-0.00432', '-0.005016', '-0.0003338', '0.0496', '0.0421', '-0.02585', '0.0473', '-0.01356', '-0.007175', '0.002985', '-0.01177', '0.003262', '0.01974', '-0.00917', '-0.00302', '-0.0382', '-0.02408', '0.01101', '-0.0333', '-0.007805', '0.0337', '-0.01807', '-0.00522', '0.001118', '0.03317', '0.05383', '0.00851', '0.02548', '0.02715', '-0.007835', '0.02396', '0.05893', '0.02666', '0.03503', '-0.0347', '-0.00797', '0.00733']",,,,,,,
mondo:0011843,hypertrophic cardiomyopathy 25,"['cardiomyopathy, hypertrophic, 25', 'hypertrophic cardiomyopathy caused by mutation in TCAP', 'Tcap hypertrophic cardiomyopathy', 'cardiomyopathy, familial hypertrophic, 25', 'cardiomyopathy, familial hypertrophic, type 25', 'CMH25', 'cardiomyopathy familial hypertrophic 25', 'hypertrophic cardiomyopathy type 25', 'TCAP hypertrophic cardiomyopathy']",0110328,607487,,C1843791,,,,C564388,,,,
mondo:0011844,myoclonic dystonia 15,"['dystonia 15, myoclonic', 'myoclonic dystonia type 15', 'dystonia-15, myoclonic', 'DYT15']",0090035,607488,210566,C1843786,,,,C538002,,,,
mondo:0011845,"migraine with or without aura, susceptibility to, 3","['MGR3', 'migraine with or without aura, susceptibility to, 3', 'migraine with or without aura, susceptibility to, type 3']",,607498,,,,,,,,,,
mondo:0011846,"bulimia nervosa, susceptibility to, 1","['bulimia nervosa, susceptibility to', 'bulimia nervosa, susceptibility to, 1', 'bulimia nervosa, susceptibility to, type 2', 'BN', 'BULN2', 'bulimia nervosa, susceptibility to, 2', 'anorexia nervosa, susceptibility to, 2', 'BULN', 'susceptibility to bulimia nervosa 2', 'BULN1']",,607499,,CN244558,,,,,,,,
mondo:0011847,"migraine without aura, susceptibility to, 4","['MGR4', 'MGOA', 'migraine without aura, susceptibility to, 4', 'migraine without aura, susceptibility to, type 4', 'common migraine']",12783,607501,,C0338480,,C117004,0005296,D020326,346.1,,,0002083
mondo:0011848,headache associated with sexual activity,"['HSA', 'benign sexual headache', 'headache associated with sexual activity']",,607504,,,,,,,,G44.82,,
mondo:0011849,psoriatic arthritis,"['psoriatic arthritis, susceptibility to', 'arthropathic psoriasis', 'psoriatic arthritis, susceptibility to, 1', 'arthritis psoriatica', 'psoriatic arthropathy', 'susceptibility to psoriatic arthritis']",9008,607507,40050,C0003872,"['0.02737', '-0.4514', '0.1547', '0.505', '-0.04132', '-0.76', '0.00932', '0.4814', '-0.3726', '-0.1917', '0.602', '0.2401', '-0.2189', '0.519', '-0.07544', '-0.4426', '-0.10724', '0.3271', '-0.4087', '-0.4521', '-0.0844', '-0.1873', '0.1445', '-0.586', '-0.4739', '-0.0879', '-0.011284', '0.2864', '0.257', '-0.2175', '0.3943', '-0.5806', '0.10626', '-0.0942', '0.2744', '-0.1093', '-0.3394', '-0.2026', '0.4124', '-0.67', '-0.0632', '-0.46', '-0.4492', '0.368', '0.3625', '0.4934', '-0.3496', '0.0421', '0.197', '0.4407', '0.12427', '0.07526', '0.3542', '-0.0448', '-0.1349', '-0.02272', '-0.3467', '-8.214e-05', '-0.499', '-0.006943', '-0.0973', '0.0888', '-0.3064', '0.426', '-0.05313', '0.938', '0.01682', '0.962', '-0.1239', '0.9463', '-0.01555', '-0.0814', '0.2388', '-0.344', '-0.114', '0.653', '-0.05682', '1.457', '-0.0595', '-0.647', '-0.8154', '-0.03592', '0.03262', '-0.0523', '0.2822', '-0.2095', '-0.3801', '0.3967', '0.12317', '0.4622', '-0.0401', '0.1257', '0.2603', '0.2153', '0.3438', '0.3638', '0.0476', '-0.4526', '-0.1727', '-0.335']",C61277,0003778,D015535,696.0,,,
mondo:0011850,"migraine with or without aura, susceptibility to, 5","['migraine with or without aura, susceptibility to, 5', 'migraine with or without aura, susceptibility to, type 5', 'Mgr5']",,607508,,,,,,,,,,
mondo:0011851,"migraine with or without aura, susceptibility to, 6","['migraine with or without aura, susceptibility to, type 6', 'migraine, familial hemiplegic, 4', 'MGR6', 'migraine with or without aura, susceptibility to, 6']",,607516,569,,,,,C564385,,,,
mondo:0011852,nonsyndromic congenital nail disorder 8,"['nail disorder, nonsyndromic congenital, type 8', 'COL7A1 inherited isolated nail anomaly', 'nail disorder, nonsyndromic congenital, 8', 'NDNC8', 'nonsyndromic congenital nail disorder type 8', 'inherited isolated nail anomaly caused by mutation in COL7A1', 'toenail dystrophy, isolated']",0080086,607523,,C1843761,,,,C564384,,,,
mondo:0011853,"Camptosynpolydactyly, complex","['CCSPD', 'camptopolydactyly, disorganisation type', 'camptosynpolydactyly, complex', 'camptopolydactyly, disorganization type']",,607539,,C1843758,"['-0.03183', '0.05634', '0.0007296', '0.004105', '-0.01278', '-0.05646', '-0.01546', '0.04156', '-0.03986', '-0.01698', '-0.01354', '-0.02606', '-0.00572', '0.02818', '-0.004', '-0.0538', '-0.02089', '-0.02888', '-0.05652', '-0.1029', '-0.00847', '-0.015045', '0.0509', '0.01955', '0.01819', '-0.012505', '0.01089', '-0.014984', '-0.01084', '-0.011986', '0.03708', '-0.005054', '0.0593', '0.0313', '0.01245', '-0.015366', '0.0129', '-0.01834', '-0.01515', '-0.05148', '0.02565', '-0.0627', '0.03357', '-0.01391', '0.004364', '-0.08295', '-0.006134', '0.007664', '0.02444', '0.04153', '-0.01195', '-0.01868', '0.02791', '0.01575', '-0.03964', '-0.005695', '0.0416', '-0.01863', '-0.0746', '0.002758', '0.014595', '0.01775', '0.0451', '0.02466', '-0.02654', '0.02354', '0.06854', '0.04346', '-0.05753', '0.07556', '-0.03143', '0.02145', '0.01505', '-0.02693', '0.0374', '0.04614', '0.02632', '0.0357', '0.0002252', '0.00785', '-0.01776', '0.01454', '0.01973', '0.0671', '0.004356', '-0.012276', '0.03607', '0.05295', '0.0797', '0.0045', '0.015305', '0.07666', '-0.01926', '0.00976', '0.11914', '0.04593', '0.02986', '-0.05768', '0.00673', '0.01475']",,,C564383,,,,
mondo:0011854,"secretory diarrhea, myopathy, and deafness","['secretory diarrhea, myopathy, and deafness']",,607540,,C1843757,,,,C564382,,,,
mondo:0011855,granular corneal dystrophy type II,"['GCDII', 'combined granular-lattice corneal dystrophy', 'CGD2', 'granular corneal dystrophy, type 2', 'GCD2', 'Avellino corneal dystrophy', 'ACD', 'corneal dystrophy, AVELLINO type', 'granular and lattice corneal dystrophies', 'avellino corneal dystrophy', 'combined granular-lattice corneal dystrophies', 'granular corneal dystrophy type 2', 'CDA', 'granular-lattice (Avellino) corneal dystrophy', 'granular-lattice corneal dystrophy', 'corneal dystrophy Avellino type']",0060444,607541,98963,C1275685,"['-0.1963', '-0.04645', '-0.5464', '0.2048', '0.2139', '-0.398', '-0.285', '0.2198', '-0.4375', '-0.509', '-0.2554', '0.0845', '-0.3699', '0.2908', '-0.1327', '-0.2499', '0.1659', '-0.699', '0.2683', '-0.8765', '-0.4153', '-0.0987', '0.3315', '0.443', '-0.329', '0.4563', '-0.2031', '0.12054', '-0.499', '0.3694', '0.6587', '0.1373', '0.1006', '0.1611', '0.0824', '0.1979', '-0.0901', '-0.376', '0.4065', '0.2524', '0.1361', '-0.304', '0.415', '0.618', '-0.1148', '0.3198', '-0.135', '0.05222', '0.1858', '0.2379', '1.24', '0.0963', '0.1604', '-0.721', '0.0265', '0.1781', '0.7603', '0.0372', '-0.6826', '0.1868', '0.06433', '-0.3403', '0.3254', '0.3174', '0.3381', '-0.2593', '1.185', '0.9814', '0.006207', '0.5283', '-0.2593', '-0.3298', '0.3608', '-0.02666', '0.6523', '0.4802', '-0.008835', '0.754', '-0.0768', '-0.208', '-0.1176', '-0.3936', '-0.4202', '0.389', '0.0566', '-0.1313', '-0.07074', '0.06573', '0.3315', '0.5244', '0.2512', '0.4983', '0.3518', '0.2502', '0.3835', '0.1976', '0.6104', '-0.803', '0.1517', '0.1405']",,,C535474,371.56,,,
mondo:0011856,spondylometaphyseal dysplasia-bowed forearms-facial dysmorphism syndrome,"['spondylometaphyseal dysplasia with bowed forearms and facial dysmorphism', 'SmD with with bowed forearms and facial dysmorphism', 'SmD with bowed forearms and Facial Dysmorphism']",0112305,607543,168552,C1843706,,,,C535791,,,,
mondo:0011857,"atrial fibrillation, familial, 3","['ATFB3', 'atrial fibrillation, familial, type 3', 'KCNQ1 familial atrial fibrillation', 'familial atrial fibrillation caused by mutation in KCNQ1', 'atrial fibrillation, familial, 3']",,607554,,C1837014,,,,C563817,,,,
mondo:0011858,"spastic paraplegia, ataxia, and intellectual disability","['spastic paraplegia, ataxia, and mental retardation', 'Spar', 'spastic paraplegia, ataxia, and intellectual disability']",,607565,,C1843661,,,,C564378,,,,
mondo:0011860,"leprosy, susceptibility to, 2","['leprosy, susceptibility to, 2', 'LPRS2']",,607572,,C1843632,,,,,,,,
mondo:0011861,breath-holding Spells,"['Bhs', 'breath-holding Spells']",,607578,,,,,,,,,,
mondo:0011862,hereditary spastic paraplegia 24,"['spastic paraplegia 24', 'SPG24', 'autosomal recessive spastic paraplegia type 24', 'autosomal recessive spastic paraplegia 24', 'spastic paraplegia 24, autosomal recessive', 'hereditary spastic paraplegia type 24']",0110775,607584,101004,C1843569,,,,C564375,,,,
mondo:0011863,prostate cancer aggressiveness quantitative trait locus on chromosome 19,"['prostate cancer aggressiveness quantitative trait locus on chromosome type 19', 'prostate cancer aggressiveness QTL', 'prostate cancer aggressiveness quantitative trait locus on chromosome 19', 'HPCqtl19']",,607592,,,,,,,,,,
mondo:0011864,"immunodeficiency, common variable, 1","['CVID1', 'antibody deficiency due to Icos defect', 'immunodeficiency, common variable', 'immunodeficiency, common variable, 1', 'immunodeficiency, common variable, type 1']",0081144,607594,,C3149378,,,,,,,,
mondo:0011866,pontocerebellar hypoplasia type 1A,"['non-syndromic pontocerebellar hypoplasia caused by mutation in VRK1', 'pontocerebellar hypoplasia with infantile spinal muscular atrophy', 'VRK1 non-syndromic pontocerebellar hypoplasia', 'pontocerebellar hypoplasia with anterior horn cell disease', 'Pch1', 'PCH1A', 'pontocerebellar hypoplasia, type 1A']",0060265,607596,,,,,,,,,,
mondo:0011867,"microphthalmia with cyst, bilateral facial clefts, and limb anomalies","['microphthalmia with cyst, bilateral facial clefts, and limb anomalies']",,607597,,C1843492,,,,C564370,,,,
mondo:0011868,lethal congenital contracture syndrome 2,"['ERBB3 lethal congenital contracture syndrome', 'LCCS2', 'lethal congenital contracture syndrome 2', 'multiple contracture syndrome, Israeli Bedouin type', 'lethal congenital contracture syndrome caused by mutation in ERBB3', 'lethal congenital contracture syndrome type 2', 'lethal congenital contractural syndrome 2', 'multiple contracture syndrome, Israeli-Bedouin type', 'multiple contracture syndrome, Israeli Bedouin type a']",0060560,607598,137783,C4275145,"['-0.4832', '-0.1849', '0.3042', '0.0019455', '-0.01645', '-0.4885', '-0.1055', '0.379', '-0.7866', '-0.3005', '-0.2168', '-0.1242', '-0.2317', '0.09686', '-0.0634', '-0.0424', '-0.001857', '0.0782', '0.01903', '-0.4744', '-0.0666', '-0.2678', '0.62', '-0.1145', '0.1683', '0.1461', '-0.3396', '0.00691', '-0.01086', '-0.307', '0.106', '-0.12415', '0.0748', '0.388', '0.0796', '-0.5537', '-0.0682', '0.1241', '-0.1471', '0.07697', '-0.1243', '-0.625', '-0.3691', '0.1915', '-0.0717', '-0.2903', '0.1881', '0.351', '0.0385', '-0.1652', '-0.2852', '-0.2057', '0.1632', '-0.493', '-0.6016', '-0.723', '0.0914', '-0.347', '-0.01117', '-0.02522', '0.3425', '0.0766', '-0.0754', '0.0791', '-0.4932', '-0.12476', '0.0883', '0.1229', '-0.3184', '0.2399', '-0.074', '0.03595', '0.0991', '-0.1153', '0.09326', '-0.1102', '-0.5444', '-0.02245', '-0.426', '-0.398', '-0.03958', '0.2247', '0.1826', '0.2189', '-0.4705', '0.1886', '0.2576', '0.555', '0.196', '-0.2266', '-0.09076', '0.4075', '0.64', '-0.1339', '0.345', '0.1169', '0.506', '-0.232', '0.1533', '0.2166']",,,C564369,,,,
mondo:0011869,epidermolysis bullosa simplex superficialis,"['EBSS', 'epidermolysis bullosa simplex superficialis']",,607600,89839,C1843477,,,,C564368,,,,
mondo:0011870,annular epidermolytic ichthyosis,"['AEI', 'ichthyosis, cyclic, with epidermolytic hyperkeratosis', 'ichthyosis, annular epidermolytic', 'epidermolytic ichthyosis, annular', 'Ciehk']",,,281139,C1843463,"['-0.1107', '0.522', '-0.718', '-0.2993', '0.5503', '-0.782', '-0.219', '-0.2263', '0.0476', '-0.5947', '-0.1915', '0.2118', '-0.326', '0.3584', '0.199', '0.546', '0.502', '-0.543', '-0.02507', '-0.899', '-0.186', '-0.0393', '0.546', '-0.5156', '-0.181', '0.6084', '-0.3718', '0.3865', '-0.789', '-0.0895', '0.4375', '-0.1818', '-0.1516', '0.4758', '-0.1532', '-0.04196', '-0.0676', '-0.1378', '-0.3357', '0.5137', '0.455', '-0.3967', '-0.1573', '-0.0465', '-0.1688', '-0.621', '-0.2847', '0.04303', '0.11536', '-0.12213', '-0.05453', '-0.823', '-0.1566', '0.04733', '-0.2328', '-0.4148', '0.7505', '0.264', '-0.3167', '0.0724', '-0.03906', '0.1092', '-0.4167', '0.5903', '0.3118', '0.2004', '0.4226', '0.561', '-0.5376', '0.935', '-0.29', '-0.3193', '0.669', '0.4355', '0.515', '0.13', '-0.4392', '0.6274', '0.155', '-0.6357', '0.2148', '-0.02379', '0.2966', '0.1743', '-0.011', '0.2786', '-0.1305', '0.7573', '0.448', '0.501', '0.5293', '0.4717', '-0.4124', '0.5415', '0.2161', '0.185', '0.4006', '-0.4138', '0.1438', '-0.09515']",,,C564367,,,,
mondo:0011871,Niemann-Pick disease type B,"['Niemann Pick disease type B', 'type B Niemann-Pick disease', 'Niemann-Pick disease, type F', 'Niemann-PICK disease, type B', 'Niemann-Pick disease, type E', 'Niemann-Pick disease, Intermediate, with visceral involvement and rapid progression']",0070112,607616,99022,C0268243,"['0.1089', '0.7534', '-0.2013', '0.1302', '0.3655', '-1.079', '-0.2974', '0.5063', '-0.376', '-0.609', '-0.473', '-0.7666', '0.2311', '0.8213', '-0.3398', '-0.31', '-0.2208', '-0.3596', '-1.174', '-0.7207', '-0.4272', '-0.674', '0.806', '-0.008896', '0.284', '-0.1582', '0.1836', '0.2301', '-0.1295', '0.3613', '0.9565', '-0.158', '0.7715', '-0.5854', '0.0482', '-0.1814', '-0.771', '0.03143', '0.08276', '-0.3313', '-0.09344', '0.1682', '-0.02565', '0.1211', '-0.4187', '0.3745', '-0.0828', '-0.422', '0.1318', '0.2095', '0.4692', '-0.2328', '0.4038', '-0.341', '-0.04733', '-0.6167', '-0.9062', '0.3843', '-0.2908', '-0.346', '-0.003826', '0.0993', '0.827', '-0.3525', '-0.2668', '-0.3179', '0.269', '-0.1098', '-0.636', '-0.5493', '-0.812', '-0.448', '-0.3362', '0.03738', '0.876', '-0.179', '0.09937', '0.157', '0.2264', '0.4575', '-0.1415', '-0.92', '0.01203', '-0.5903', '-0.4927', '-0.1549', '0.7417', '0.1349', '1.196', '0.447', '0.1417', '0.6963', '-0.5327', '0.067', '0.1472', '0.2114', '-0.3333', '-0.1359', '0.7495', '-0.3196']",C126866,,D052537,,E75.241,,
mondo:0011872,Griscelli syndrome type 2,"['Griscelli disease type 2', 'PAID syndrome', 'hypopigmentation-immunodeficiency with or without neurologic impairment syndrome', 'Griscelli syndrome, type 2', 'Griscelli-Pruniéras syndrome type 2', 'GS2', 'Griscelli-PruniC)ras syndrome type 2', 'Paid syndrome', 'partial albinism and immunodeficiency syndrome', 'Griscelli syndrome with hemophagocytic syndrome', 'Griscelli-Pruni��ras syndrome type 2']",0060833,607624,79477,C1868679,"['0.1361', '0.785', '-0.11694', '-0.5254', '-0.2101', '-0.5107', '-0.3806', '-0.1869', '-0.1015', '-0.08624', '0.05917', '-0.2969', '-0.286', '0.2194', '-0.335', '-0.3132', '0.1162', '0.1478', '-0.2059', '-0.52', '-0.3333', '-0.208', '0.2422', '-0.1274', '-0.2732', '0.0839', '-0.4695', '-0.07434', '-0.2925', '-0.003752', '0.858', '0.2073', '0.2825', '0.1201', '0.3262', '0.423', '-0.01252', '-0.08514', '-0.0942', '-0.2642', '0.3367', '-0.2023', '0.2107', '-0.0828', '-0.8325', '-0.1776', '-0.2434', '-0.634', '0.4944', '-0.2214', '0.0986', '0.1627', '0.5674', '-0.026', '-0.02223', '0.05286', '0.0827', '0.3286', '0.1053', '0.07086', '-0.01749', '0.3723', '-0.06305', '0.0888', '0.1954', '-0.1613', '0.327', '0.3445', '-0.4353', '0.9536', '-0.3538', '-0.458', '-0.1482', '0.6196', '-0.1641', '-0.2367', '-0.211', '0.538', '-0.1517', '-0.1025', '-0.0739', '-0.603', '0.2113', '0.2876', '-0.8013', '-0.2317', '0.5005', '0.406', '0.4985', '0.507', '0.3906', '0.1283', '0.1248', '-0.0906', '0.4788', '0.8696', '0.1322', '-0.3691', '0.0106', '0.379']",C111814,,C537302,,E70.3,,
mondo:0011873,"Niemann-Pick disease, type C2","['Niemann-Pick disease type C2', 'NPC2', 'Niemann-PICK disease, type C2', 'type C2 Niemann-Pick disease', 'Niemann-Pick disease, type C2']",0070114,607625,,C1843366,,C126865,,C536119,,,,
mondo:0011874,neonatal ichthyosis-sclerosing cholangitis syndrome,"['IHSC', 'NISCH syndrome', 'Nisch syndrome', 'ILVASC', 'Ilvasc', 'ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis', 'neonatal ichthyosis-sclerosing cholangitis syndrome', 'ichthyosis-hypotrichosis-sclerosing cholangitis syndrome', 'ichthyosis-sclerosing cholangitis syndrome']",,607626,59303,C1843355,"['0.0976', '0.1874', '-0.2954', '-0.2817', '0.2568', '-0.2167', '-0.1366', '-0.10944', '0.694', '0.3047', '-0.55', '-0.6177', '-0.097', '0.0264', '-0.4397', '0.083', '0.5073', '-0.735', '-0.009796', '-1.146', '-0.3865', '-0.1887', '0.4922', '-0.0307', '0.0879', '0.1625', '-0.1317', '0.721', '0.03195', '-0.4216', '1.081', '0.4082', '0.1853', '0.03915', '0.2766', '-0.4658', '-1.087', '-0.54', '0.03326', '0.1439', '-0.627', '-0.2059', '0.2852', '0.1992', '-0.303', '-0.08167', '-0.3696', '-0.289', '-0.0624', '-0.6865', '-0.2394', '-0.3264', '0.0726', '0.53', '-0.822', '-0.2156', '0.736', '-0.09875', '-0.4436', '-0.2443', '0.0664', '0.4402', '0.3445', '-0.693', '0.3545', '0.1666', '0.923', '0.7256', '-0.6333', '0.467', '-0.641', '-0.2429', '-0.06586', '0.5464', '-0.02039', '0.03827', '0.342', '-0.553', '0.1584', '0.10455', '0.597', '0.2974', '-0.4556', '0.1346', '0.02812', '0.3496', '-0.1825', '0.3193', '0.00911', '0.3694', '0.3289', '0.2377', '-0.3372', '0.673', '1.097', '-0.4077', '0.1012', '-0.1678', '0.4663', '-0.0945']",,,C564365,,,,
mondo:0011875,"epilepsy, idiopathic generalized, susceptibility to, 11","['CLCN2 generalised epilepsy', 'epilepsy, idiopathic generalized, susceptibility to, 11', 'EIG11', 'generalized epilepsy caused by mutation in CLCN2', 'epilepsy, juvenile absence, susceptibility to, 2', 'susceptibility to idiopathic generalized epilepsy 11', 'generalised epilepsy caused by mutation in CLCN2', 'epilepsy, juvenile myoclonic, susceptibility to, 8', 'CLCN2 generalized epilepsy', 'susceptibility to idiopathic generalised epilepsy 11', 'epilepsy, idiopathic generalized, susceptibility to, type 11']",0111312,607628,,,,,,,,,,
mondo:0011876,juvenile absence epilepsy,"['epilepsy juvenile absence', 'susceptibility to juvenile absence epilepsy 1', 'EJA1', 'epilepsy, juvenile absence, susceptibility to, 1', 'JAE', 'epilepsy, juvenile absence, susceptibility to, type 1']",0060172,,1941,C4317339,"['1.115', '0.1927', '-0.3606', '-0.31', '-0.2261', '-0.2393', '0.9185', '0.4443', '-0.6284', '-0.637', '0.07733', '-0.417', '-0.4346', '0.35', '0.0387', '-0.121', '-0.4497', '-0.76', '-0.2852', '-0.5913', '-0.212', '0.325', '0.0255', '-0.781', '-0.2976', '-0.01819', '-0.1315', '-0.24', '-0.4094', '0.2878', '0.511', '-0.871', '0.2898', '0.2177', '0.744', '0.2712', '-0.0198', '0.3188', '-0.1636', '-0.2874', '0.012695', '-0.4626', '0.1298', '-0.6133', '-0.1871', '-0.592', '-0.3838', '0.3308', '0.4597', '0.766', '-0.0916', '0.09827', '-0.0509', '-0.294', '0.0645', '-0.2494', '-0.02356', '0.065', '-0.03784', '0.1309', '-0.8115', '0.5503', '0.469', '-0.3813', '-0.2795', '1.385', '0.1682', '0.0011425', '-0.7446', '0.4453', '0.951', '0.5845', '-0.00936', '-0.2683', '0.421', '0.7446', '1.028', '0.305', '-0.5996', '0.2708', '0.07056', '0.582', '0.551', '0.00591', '0.2717', '0.04047', '0.012085', '0.6475', '0.647', '0.4744', '0.1227', '-0.0056', '-0.335', '-0.04913', '0.1882', '0.3145', '0.535', '-0.392', '0.4226', '0.08014']",C129868,,,,,,
mondo:0011877,autosomal dominant osteopetrosis 1,"['osteopetrosis, autosomal dominant 1', 'osteopetrosis autosomal dominant type 1', 'osteopetrosis, autosomal dominant type 1', 'osteopetrosis, autosomal dominant, type 1', 'OPTA1', 'autosomal dominant osteopetrosis type 1', 'LRP5 osteopetrosis (disease)']",0110937,607634,2783,C1843330,"['0.11456', '0.04428', '0.3035', '-0.615', '0.2164', '-0.265', '0.0903', '1.041', '-0.0913', '-0.2502', '-0.1016', '-0.4043', '-0.3142', '-0.06143', '0.2803', '0.271', '0.1636', '-0.86', '-0.2098', '-0.717', '0.1202', '-0.3958', '0.5547', '-0.2327', '0.3008', '0.3672', '0.06186', '-0.5176', '-0.4326', '-0.172', '0.1661', '0.513', '0.1724', '-0.0297', '-0.1742', '-0.344', '0.3096', '-0.6465', '-0.2206', '-0.1842', '-0.06183', '-0.12036', '-0.02682', '0.1118', '-0.12195', '-0.831', '-0.1121', '-0.409', '0.3286', '-0.1086', '-0.05267', '0.2052', '0.0965', '0.0907', '0.1073', '-0.4558', '-0.03937', '0.2094', '0.0408', '0.313', '0.4597', '-0.2563', '-0.2119', '-0.3176', '-0.1045', '-0.1677', '0.3677', '0.965', '-0.3818', '0.3435', '-0.227', '-0.2416', '-0.1678', '-0.007336', '0.527', '-0.2644', '-0.34', '0.9644', '0.3428', '-0.3123', '-0.07574', '-0.376', '0.1858', '0.2964', '-0.54', '0.0673', '0.1842', '0.10516', '0.0922', '0.287', '-0.4119', '0.03235', '-0.635', '0.1719', '0.579', '0.2983', '0.5', '-0.29', '0.2327', '0.1982']",,,C536056,,,,
mondo:0011879,"neuronopathy, distal hereditary motor, type 7B","['HMN7B', 'Lower motor neuron disease, dynactin type', 'neuronopathy, distal hereditary motor caused by mutation in DCTN1', 'neuropathy, distal hereditary motor, type 7B', 'HMN 7B', 'neuropathy, distal hereditary motor, with vocal cord paralysis, type 7B', 'DCTN1 neuronopathy, distal hereditary motor', 'neuronopathy, distal hereditary motor, type VIIB', 'Dhmn7B']",0111202,607641,,C1843315,,,,C564362,,,,
mondo:0011880,"candidiasis, familial, 3","['candidiasis, familial, 3', 'Fcnc', 'CANDF3', 'candidiasis, familial chronic nail, with Icam1 deficiency']",,607644,,C1843306,,,,C564361,,,,
mondo:0011881,keratosis palmoplantaris striata 3,"['keratoderma, palmoplantar, striate form 3', 'keratosis palmoplantaris striata III', 'KRT1 striate palmoplantar keratoderma', 'striate palmoplantar keratoderma 3', 'striate palmoplantar keratoderma caused by mutation in KRT1', 'keratosis palmoplantaris striata type 3', 'PPKS3', 'keratoderma palmoplantar striate form 3']",0081110,607654,,C2931123,,,,C536163,,,,
mondo:0011882,skin fragility-woolly hair-palmoplantar keratoderma syndrome,"['skin fragility-woolly hair-palmoplantar hyperkeratosis syndrome', 'SFWHS', 'skin fragility wooly hair syndrome', 'skin fragility-woolly hair syndrome', 'skin fragility woolly hair syndrome']",,607655,293165,C1843292,"['-0.05463', '0.11487', '-0.0569', '-0.2627', '0.1382', '-0.2593', '0.07104', '0.00751', '0.05365', '-0.02426', '-0.1328', '0.05664', '-0.4536', '-0.0682', '-0.1427', '0.2241', '0.4204', '-0.429', '-0.0882', '-0.923', '-0.1764', '0.09735', '0.2832', '-0.0446', '-0.0509', '0.2603', '-0.12274', '0.1954', '0.1381', '-0.2888', '0.1711', '-0.1278', '0.074', '0.2598', '0.1927', '0.01002', '-0.1294', '-0.1276', '-0.1376', '-0.2289', '0.0954', '-0.2413', '-0.07697', '-0.2189', '-0.2018', '-0.1526', '-0.2983', '0.2556', '0.01881', '-0.0641', '-0.1305', '-0.0957', '0.6064', '0.2563', '-0.295', '-0.05197', '0.3718', '-0.0978', '-0.3896', '-0.314', '0.1097', '0.006657', '-0.2815', '-0.2651', '0.1772', '0.10803', '0.4436', '0.3713', '-0.1698', '0.4888', '-0.5796', '-0.1812', '0.0458', '0.05386', '-0.03516', '-0.4165', '0.2012', '-0.11444', '0.1094', '-0.2427', '8.523e-05', '0.2097', '0.0957', '0.0794', '0.0447', '-0.11945', '-0.0824', '0.588', '0.4307', '0.2664', '0.4082', '0.2322', '0.1874', '0.3796', '0.3245', '0.06122', '0.2766', '-0.264', '0.2494', '0.2272']",,,C564359,,,,
mondo:0011883,Curly hair - acral keratoderma - caries syndrome,"['Curly hair - acral keratoderma - caries syndrome', 'Chacs', 'CHACS', 'Chac syndrome']",,607656,307766,,,,,C536220,,,,
mondo:0011884,hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome,"['hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome', 'Hopp syndrome', 'hypotrichosis-striate palmoplantar hyperkeratosis-acroosteolysis-periodontitis syndrome', 'hypotrichosis-striate palmoplantar keratoderma-acroosteolysis-periodontitis syndrome', 'HOPP syndrome', 'hypotrichosis-osteolysis-periodontitis-palmoplantar hyperkeratosis syndrome']",,607658,307936,C1843285,,,,C564357,,,,
mondo:0011885,tubulointerstitial nephritis and uveitis syndrome,"['Tubulointerstitial nephritis and uveitis', 'acute Tubulointerstitial nephritis', 'TINU syndrome', 'acute tubulointerstitial nephritis and uveitis syndrome', 'TUBULOINTERSTITIAL nephritis with uveitis', 'Dobrin syndrome', 'TINU']",,607665,91500,C1843273,,C123021,,C536922,,N10,10069039,
mondo:0011886,torsion dystonia 13,"['torsion dystonia type 13', 'primary dystonia with mixed phenotype', 'DYT13', 'dystonia 13, torsion, autosomal dominant', 'primary dystonia, DYT13 type', 'primary torsion dystonia with predominant craniocervical or upper limb onset']",0090037,607671,98807,,,,,C564354,,,,
mondo:0011887,"cataract, congenital, with mental impairment and dentate gyrus atrophy","['cataract, congenital, with mental impairment and dentate gyrus atrophy']",,607674,,C1843257,,,,C564353,,,,
mondo:0011888,immunodeficiency 67,"['invasive pneumococcal disease, protection against', 'immunodeficiency due to interleukin-1 receptor-associated kinase-4 deficiency', 'invasive pneumococcal disease, recurrent isolated, 1', 'IPD1', 'IRAK4 deficiency', 'invasive pneumococcal disease, recurrent isolated, type 1', 'IRAK-4 deficiency', 'Interleukin receptor-associated kinase deficiency', 'IRAK4D']",,607676,70592,C1843256,"['0.068', '0.06192', '-0.3696', '-0.0566', '0.009155', '-0.452', '0.517', '-0.02325', '0.0587', '-0.437', '-0.3564', '0.285', '-0.2479', '0.04062', '-0.214', '-0.0754', '-0.2957', '0.2869', '-0.3806', '-0.5103', '0.0626', '-0.4421', '0.3784', '-0.7803', '-0.0594', '-0.1898', '-0.7905', '0.0483', '-0.2439', '-0.372', '-0.04025', '0.2842', '0.11096', '0.42', '0.2493', '-0.1116', '-0.5415', '-0.605', '-0.3645', '0.00796', '-0.3691', '-0.03635', '0.01651', '-0.2034', '-0.537', '-0.1454', '-0.1277', '-0.4597', '0.09906', '0.4204', '-0.0824', '-0.6245', '0.2954', '0.301', '0.299', '0.4077', '0.514', '-1.095', '-0.3413', '0.4019', '0.366', '0.9644', '-0.389', '0.4124', '0.6294', '-0.2109', '0.2861', '0.663', '-0.344', '0.635', '-0.2834', '-0.01542', '-0.3933', '-0.161', '0.495', '0.04636', '0.403', '0.2646', '0.2854', '0.2448', '0.0763', '0.229', '0.0545', '0.418', '-0.04813', '0.2666', '0.5728', '0.314', '-0.003666', '0.1247', '0.489', '0.351', '-0.3406', '-0.02275', '0.6865', '0.8076', '0.1694', '-0.3147', '-0.2778', '-0.2433']",,,C564352,,,,
mondo:0011889,Charcot-Marie-Tooth disease type 2I,"['Charcot-Marie-Tooth disease, axonal, type 2I', 'Charcot-Marie-Tooth neuropathy, type 2I', 'Charcot Marie Tooth disease type 2I', 'Charcot-Marie-Tooth neuropathy type 2I', 'CMT2I', 'autosomal dominant Charcot-Marie-Tooth disease type 2I', 'CMT 2I', 'Charcot-Marie-Tooth disease, type 2I']",0110158,607677,99942,CN207466,"['0.1139', '0.3743', '0.3074', '-0.07855', '0.03464', '-0.03442', '0.0939', '0.5107', '-0.8105', '-0.15', '-0.07684', '0.4277', '-0.4167', '0.4329', '-0.2078', '-0.03735', '-0.3318', '-0.5767', '-0.6367', '-0.6807', '0.2214', '0.2815', '0.10364', '0.708', '0.0893', '0.2328', '-0.01697', '0.2349', '0.01311', '0.02403', '0.1415', '-0.725', '-0.097', '0.3025', '0.5825', '-0.696', '-0.699', '-0.1046', '0.2595', '-0.1698', '-1.597', '-0.538', '-0.1283', '0.3696', '-0.2727', '-0.3494', '0.00379', '-0.001848', '-0.0855', '0.03677', '0.5073', '0.463', '-0.2063', '-1.103', '0.3132', '-0.1251', '-0.1572', '0.4097', '-0.8867', '-0.2878', '-0.3767', '-0.1067', '0.8423', '0.681', '-0.8027', '1.241', '-0.02187', '0.5356', '-0.569', '0.4844', '-0.689', '0.04742', '0.555', '-0.2356', '1.47', '0.5767', '-0.2756', '0.4932', '0.07733', '-0.4846', '-0.3823', '-0.2069', '0.7207', '0.8584', '0.1326', '-0.1421', '-0.02617', '0.5317', '0.6333', '0.3877', '-0.02695', '-0.0866', '0.171', '0.2034', '0.4844', '0.5967', '0.6255', '-0.579', '-0.2148', '0.757']",,,,,,,
mondo:0011890,Charcot-Marie-Tooth disease type 1D,"['Charcot-Marie-Tooth disease type 1 caused by mutation in EGR2', 'HMSN ID', 'hereditary motor and sensory neuropathy 1D', 'Charcot Marie Tooth disease type 1D', 'CMT 1D', 'CMT1D', 'HMSN 1D', 'Charcot-Marie-Tooth disease, demyelinating, type 1D', 'HMSN1D', 'Charcot-Marie-Tooth neuropathy type 1D', 'Charcot-Marie-Tooth neuropathy, type 1D', 'EGR2 Charcot-Marie-Tooth disease type 1', 'Charcot-Marie-Tooth disease, type 1D']",0110150,607678,101084,C1843247,"['0.0695', '0.0638', '0.2717', '0.05875', '-0.11755', '-0.02336', '0.074', '0.429', '-1.051', '-0.6333', '-0.0316', '0.549', '-0.5034', '0.763', '-0.3445', '-0.568', '-0.2634', '-0.852', '-0.3896', '-0.5674', '0.3347', '0.274', '0.1982', '0.893', '0.3645', '0.6284', '0.3188', '0.4927', '0.375', '0.0648', '-0.4817', '-0.6826', '0.10614', '0.1505', '0.4153', '-0.981', '-0.853', '-0.2275', '0.4133', '-0.3223', '-0.981', '-0.0903', '-0.2257', '0.689', '-0.02191', '0.1497', '0.09686', '-0.1835', '-0.1482', '0.3687', '0.12274', '0.2654', '-0.3037', '-1.211', '0.254', '-0.418', '0.11365', '0.505', '-0.7036', '-0.2471', '-0.1652', '0.07574', '0.54', '0.7285', '-0.5547', '1.354', '-0.0733', '0.6216', '-0.5337', '0.348', '-0.4946', '0.0753', '0.527', '0.02977', '1.28', '0.564', '-0.1893', '0.1866', '-0.0677', '-0.996', '0.0709', '0.04022', '0.7056', '0.6743', '-0.3372', '0.04214', '0.3474', '0.529', '0.949', '-0.0594', '-0.3372', '0.1985', '-0.06158', '0.05484', '0.327', '0.5215', '0.968', '-0.3174', '0.0284', '0.0656']",,,C537985,,,,
mondo:0011891,"febrile seizures, familial, 8","['GABRG2 generalised epilepsy with febrile seizures plus', 'epilepsy, childhood absence, susceptibility to, 2', 'generalised epilepsy with febrile seizures plus, type 3', 'Gefs+, type 3', 'childhood absence epilepsy caused by mutation in GABRG2', 'GABRG2 generalized epilepsy with febrile seizures plus', 'generalized epilepsy with febrile seizures plus caused by mutation in GABRG2', 'ECA2', 'generalized epilepsy with febrile seizures plus, type 3', 'GABRG2 childhood absence epilepsy', 'epilepsy, childhood absence, susceptibility to, type 2', 'generalised epilepsy with febrile seizures plus caused by mutation in GABRG2', 'susceptibility to childhood absence epilepsy 2', 'GEFSP3']",0111298,611277,,C1858674,,,,C565811,,,,
mondo:0011892,"epilepsy, idiopathic generalized, susceptibility to, 9","['generalized epilepsy caused by mutation in CACNB4', 'generalised epilepsy caused by mutation in CACNB4', 'CACNB4 generalised epilepsy', 'epilepsy, idiopathic generalized, susceptibility to, 9', 'CACNB4 generalized epilepsy', 'epilepsy, idiopathic generalized, susceptibility to, type 9', 'susceptibility to idiopathic generalized epilepsy 9', 'susceptibility to idiopathic generalised epilepsy 9', 'EIG9', 'epilepsy, juvenile myoclonic, susceptibility to, 6']",0111323,607682,,,,,,,,,,
mondo:0011893,autosomal dominant nonsyndromic hearing loss 52,"['autosomal dominant deafness 52', 'DFNA52', 'autosomal dominant nonsyndromic deafness 52', 'deafness, autosomal dominant 52', 'deafness, autosomal dominant 42', 'autosomal dominant nonsyndromic deafness type 52']",0110578,607683,,C1843232,,,,C564348,,,,
mondo:0011894,Charcot-Marie-Tooth disease type 2E,"['Charcot-Marie-Tooth neuropathy, type 2E', 'CMT 2E', 'Charcot-Marie-Tooth neuropathy type 2E', 'NEFL Charcot-Marie-Tooth disease type 2', 'CMT2E', 'Charcot-Marie-Tooth disease, axonal, type 2E', 'Charcot-Marie-Tooth disease type 2 caused by mutation in NEFL', 'Charcot-Marie-Tooth disease, type 2E', 'autosomal dominant Charcot-Marie-Tooth disease type 2E', 'Charcot Marie Tooth disease type 2E']",0110165,607684,99939,,"['0.2374', '0.2482', '-0.1425', '-0.001597', '0.04285', '-0.5713', '-0.1214', '0.944', '-0.742', '-0.0382', '0.1948', '0.6997', '-0.27', '0.41', '-0.272', '-0.1594', '-0.1547', '-1.117', '-0.476', '-0.6816', '0.03207', '0.4075', '-0.09406', '0.5625', '0.557', '0.3203', '-0.2163', '0.5244', '0.06696', '0.02339', '0.071', '-0.4807', '0.2766', '0.1077', '0.3264', '-0.639', '-0.4138', '0.00152', '0.3296', '-0.1927', '-1.374', '0.2252', '0.1615', '0.10156', '-0.1881', '-0.2268', '0.05905', '-0.2278', '-0.4666', '-0.06067', '0.3318', '0.4277', '-0.24', '-1.212', '0.604', '-0.1951', '0.2275', '-0.1199', '-0.4858', '-0.1533', '-0.489', '0.11365', '0.4417', '0.6055', '-1.067', '1.309', '0.08325', '0.716', '-0.4285', '0.4133', '-0.4207', '0.00686', '0.4058', '-0.339', '1.456', '0.7026', '-0.2374', '0.3806', '-0.01932', '-0.3916', '-0.239', '-0.1763', '0.9346', '0.9736', '0.08606', '-0.2686', '0.1901', '0.576', '0.7407', '0.1434', '0.2185', '0.12354', '0.279', '0.488', '0.8413', '0.7554', '0.4124', '-0.3254', '-0.2472', '0.9653']",C134953,,C537994,,,,
mondo:0011895,idiopathic hypereosinophilic syndrome,"['HES', 'hypereosinophilic syndrome, idiopathic', 'hypereosinophilic syndrome, idiopathic, resistant to imatinib, isolated cases, somatic mutation']",,607685,3260,C0206141,,,,,,,,
mondo:0011896,"Parkinson disease 11, autosomal dominant, susceptibility to","['Parkinson disease 11, autosomal dominant, susceptibility to', 'GIGYF2 hereditary late onset Parkinson disease', 'susceptibility to autosomal dominant Parkinson disease 11', 'hereditary late onset Parkinson disease caused by mutation in GIGYF2', 'PARK11', 'Parkinson disease 11']",,607688,,C1843211,,,,C564345,,,,
mondo:0011897,leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome,"['hypomyelination-cerebellar atrophy-hypoplasia of the corpus callosum syndrome', 'ataxia, delayed dentition, and hypomyelination', 'leukoencephalopathy, hypomyelinating, with ataxia and delayed dentition', 'leukodystrophy, hypomyelinating, 7, with or without oligodontia and/or hypogonadotropic hypogonadism', 'leukodystrophy, hypomyelinating, with hypodontia and hypogonadotropic hypogonadism', 'leukoencephalopathy-ataxia-hypodontia-hypomyelination syndrome', '4H syndrome', 'HLD7', 'hypomyelinating leukodystrophy-ataxia-hypodontia-hypomyelination syndrome', 'dentoleukoencephalopathy', 'hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism', 'ataxia-delayed dentition-hypomyelination syndrome', 'ataxia-delayed dentition-hypomyelination syndrome; odontoleukodystrophy']",0060794,607694,88637,,"['-0.419', '0.00268', '-0.1154', '-0.06335', '-0.0402', '-0.3848', '-0.1103', '0.4492', '-0.4114', '-0.1998', '-0.3015', '-0.04382', '-0.268', '-0.2415', '0.3735', '-0.3506', '0.0366', '0.05045', '-0.5557', '-0.509', '0.1979', '-0.1969', '-0.2744', '-0.2654', '0.2598', '0.0003839', '-0.12225', '0.01775', '0.37', '-0.5396', '0.2122', '0.1626', '0.1921', '-0.0986', '0.1427', '-0.1427', '-0.0587', '-0.3738', '-0.2227', '-0.1877', '0.1348', '-0.04507', '-0.09607', '0.03506', '0.03754', '-0.322', '0.12335', '0.2327', '-0.3777', '-0.607', '0.2417', '0.293', '-0.2101', '-0.00258', '-0.3962', '0.003092', '0.448', '-0.2686', '-0.6055', '0.3906', '0.1284', '0.1505', '0.2778', '0.2908', '-0.3713', '-0.01516', '0.2886', '0.3857', '-0.2155', '0.1365', '-0.3445', '0.1968', '0.3213', '-0.2793', '0.317', '-0.004066', '-0.02719', '0.156', '0.1326', '0.04895', '0.05423', '0.097', '-0.3203', '0.2788', '0.04346', '-0.2286', '0.2032', '0.05414', '0.1271', '0.010895', '0.3835', '0.3584', '0.3657', '-0.272', '0.8237', '0.1301', '0.0977', '-0.1372', '-0.0648', '0.3433']",,,,,,,
mondo:0011898,"Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive","['Charcot-Marie-Tooth neuropathy, axonal, with vocal cord paresis, autosomal recessive', 'Charcot-Marie-Tooth disease, type 4A, axonal form', 'Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive', 'CMT2 with vocal cord paresis, autosomal recessive']",,607706,,C1843183,,,,,,,,
mondo:0011899,Noonan syndrome-like disorder with loose anagen hair,"['NS/LAH', 'NSLH1', 'Tosti syndrome', 'Noonan syndrome-like disorder with loose anagen hair 1', 'Noonan-like syndrome with loose anagen hair', 'Noonan syndrome-like disorder with loose anagen hair', 'NSLH']",0080691,,2701,C3501846,"['-0.007263', '-0.04068', '0.4426', '-0.2983', '-0.1132', '0.1156', '0.1371', '0.934', '-0.497', '-0.714', '0.517', '-0.339', '0.2427', '0.0864', '-0.2793', '0.3096', '-0.0867', '-0.3992', '-0.8833', '-0.2869', '-0.185', '0.1248', '-0.04044', '-0.623', '0.168', '-0.2107', '-0.5347', '0.529', '1.098', '0.1858', '0.463', '-0.5854', '0.2842', '0.6157', '-0.582', '-0.1827', '-0.2219', '0.7095', '0.1842', '-0.5664', '0.3806', '0.7075', '0.07574', '-0.03812', '0.011215', '-0.1929', '-0.006985', '0.2495', '0.2769', '-0.354', '-0.0399', '0.236', '-0.2104', '0.532', '-0.7393', '-0.4612', '-0.005398', '0.2208', '-0.0632', '-0.3245', '0.3472', '-0.373', '0.5005', '-0.2267', '0.7124', '-0.1711', '-0.04797', '0.2214', '0.04132', '0.7534', '0.2119', '0.3413', '-0.0567', '0.2233', '0.342', '-0.006077', '0.5967', '-0.07434', '0.36', '-0.1791', '0.6895', '-0.3318', '-0.1334', '-0.2361', '-0.0499', '-0.5283', '0.45', '-0.1223', '1.052', '1.244', '0.0314', '0.2339', '-0.2708', '-0.12494', '0.8633', '-0.374', '0.38', '-0.1167', '0.2556', '0.04016']",C178129,,C564342,,,,
mondo:0011900,"porokeratosis 4, disseminated superficial actinic type","['porokeratosis 4, disseminated superficial actinic type', 'porokeratosis 4, disseminated superficial actinic', 'porokeratosis, disseminated superficial actinic, 2', 'POROK4']",,607728,,C1843180,,,,,,,,
mondo:0011901,Charcot-Marie-Tooth disease axonal type 2H,"['Charcot-Marie-Tooth disease, axonal, with pyramidal features, autosomal recessive', 'Charcot-Marie-Tooth disease type 2H', 'Charcot Marie Tooth disease type 2H', 'CMT2H', 'axonal Charcot-Marie-Tooth disease with pyramidal involvement', 'autosomal recessive axonal Charcot-Marie-Tooth neuropathy with pyramidal features', 'autosomal recessive axonal Charcot-Marie-Tooth disease with pyramidal features', 'autosomal recessive axonal CMT4C2', 'Charcot-Marie-Tooth neuropathy, axonal, with pyramidal features, autosomal recessive', 'Charcot-Marie-Tooth disease, axonal, type 2H', 'AR-CMT2C', 'CMT 2H']",0110166,607731,101102,C1843173,,,,C535415,,,,
mondo:0011902,Charcot-Marie-Tooth disease type 1F,"['NEFL Charcot-Marie-Tooth disease type 1', 'CMT 1F', 'Charcot Marie Tooth disease type 1F', 'Charcot-Marie-Tooth disease type 1 caused by mutation in NEFL', 'Charcot-Marie-Tooth disease, demyelinating, type 1F', 'Charcot-Marie-Tooth neuropathy, type 1F', 'CMT1F', 'Charcot-Marie-Tooth neuropathy type 1F', 'Charcot-Marie-Tooth disease, type 1F']",0110149,607734,101085,C1843164,"['-0.0761', '0.424', '0.3347', '0.289', '-0.10535', '-0.1503', '-0.2874', '0.4795', '-0.947', '-0.2427', '-0.04907', '0.2712', '-0.015076', '0.3125', '-0.07947', '-0.4087', '0.1945', '-0.217', '-0.0943', '-0.614', '0.10535', '0.4834', '0.6973', '0.847', '0.265', '0.3962', '0.0001842', '0.526', '0.2251', '-0.3845', '-0.1833', '-0.4346', '0.1354', '0.361', '0.2969', '-0.646', '-0.5674', '0.092', '0.2017', '-0.5117', '-1.219', '-0.4768', '-0.478', '0.4868', '-0.373', '-0.4175', '-0.02684', '-0.05405', '-0.264', '0.12366', '0.3208', '0.0519', '0.0009613', '-0.7524', '0.764', '-0.1483', '0.06018', '0.1514', '-0.2164', '-0.1732', '-0.6616', '0.2402', '1.276', '0.8735', '-0.6973', '1.206', '-0.08136', '1.027', '-0.3696', '0.3945', '-0.7886', '-0.0808', '0.387', '-0.1528', '1.252', '0.5923', '-0.1919', '0.518', '0.2996', '-0.5425', '0.2222', '-0.3252', '0.796', '0.6587', '0.3103', '-0.5483', '-0.167', '0.5747', '0.858', '0.03497', '0.403', '-0.007008', '0.1267', '0.286', '0.542', '0.5205', '0.607', '-0.6665', '-0.0698', '0.3164']",,,C537987,,,,
mondo:0011903,Charcot-Marie-Tooth disease type 2J,"['CMT2J', 'Charcot-Marie-Tooth disease type 2 with hearing loss and pupillary abnormalities', 'Charcot Marie Tooth disease type 2J', 'Charcot-Marie-Tooth disease, type 2J', 'Charcot-Marie-Tooth neuropathy, type 2J', 'Charcot-Marie-Tooth neuropathy type 2J', 'Charcot-Marie-Tooth disease, axonal, type 2J', 'Charcot-Marie-Tooth disease, type 2, with hearing loss and pupillary abnormalities', 'autosomal dominant Charcot-Marie-Tooth disease type 2J', 'CMT 2J']",0110157,607736,99943,,"['0.2463', '0.2213', '0.2307', '0.1183', '-0.02681', '-0.2107', '0.2222', '0.4453', '-0.867', '-0.1747', '-0.00984', '0.515', '-0.5786', '0.3154', '-0.3083', '-0.2173', '-0.3157', '-0.5005', '-0.628', '-0.8096', '0.0318', '0.2598', '0.058', '0.6846', '0.219', '0.003677', '-0.0733', '-0.005287', '0.1472', '0.04422', '0.257', '-0.8843', '0.10565', '0.02979', '0.2717', '-0.621', '-0.7344', '-0.1974', '0.11786', '-0.0772', '-1.46', '-0.3955', '-0.05725', '0.4138', '-0.2546', '-0.3364', '0.1858', '-0.0703', '-0.1165', '0.159', '0.2703', '0.2434', '-0.271', '-0.9756', '0.328', '-0.2007', '-0.06137', '0.4084', '-0.652', '-0.2079', '-0.1533', '-0.1741', '0.711', '0.6797', '-0.8794', '1.259', '-0.2229', '0.6987', '-0.4524', '0.656', '-0.6953', '0.1605', '0.649', '-0.2646', '1.204', '0.3657', '-0.326', '0.648', '0.1744', '-0.5103', '-0.0621', '-0.068', '0.7847', '0.8013', '0.2915', '-0.2145', '0.1926', '0.2905', '0.602', '0.3606', '0.2039', '-0.01094', '0.162', '0.4583', '0.399', '0.5874', '0.7256', '-0.6875', '-0.3901', '0.6187']",,,C535417,,,,
mondo:0011904,"seizures, benign familial infantile, 3","['BFIS3', 'convulsions, benign familial infantile, 3', 'benign familial infantile convulsions', 'seizures, benign familial neonatal-infantile', 'seizures, benign familial infantile, type 3', 'benign familial infantile epilepsy caused by mutation in SCN2A', 'BFNIS', 'benign neonatal-infantile epilepsy', 'epilepsy, benign neonatal-infantile', 'SCN2A benign familial infantile epilepsy', 'seizures, benign familial infantile, 3', 'convulsions benign familial neonatal']",0081116,607745,140927,C1843140,"['0.1958', '-0.01685', '-0.0605', '0.1487', '-0.4604', '-0.3582', '0.995', '0.2795', '-0.2334', '-0.546', '-0.3186', '-0.3828', '-0.358', '0.813', '-0.362', '0.1549', '-0.10583', '-0.0874', '-0.3367', '-0.4863', '-0.05045', '0.7144', '0.0835', '-0.2184', '0.0934', '-0.1893', '0.0653', '-0.1113', '-0.2737', '0.7544', '0.0005827', '-0.1831', '0.4631', '0.4243', '0.3684', '0.4392', '-0.1415', '-0.276', '0.1681', '-0.635', '-0.3088', '-0.365', '-0.1525', '-0.3538', '0.1853', '-0.347', '-0.10767', '0.675', '0.517', '0.9795', '-0.02399', '0.3657', '0.3489', '-0.3171', '0.0897', '0.2498', '0.0325', '0.1562', '-0.2102', '-0.2241', '-0.3914', '0.3738', '0.614', '0.02333', '-0.869', '1.339', '0.1951', '-0.3333', '-0.9536', '0.8022', '0.593', '0.658', '0.03098', '-0.628', '0.5913', '0.7563', '0.7246', '0.6533', '-0.2118', '-0.1497', '0.01962', '1.011', '0.436', '0.11255', '0.1866', '-0.08154', '0.1262', '0.9805', '0.644', '1.103', '0.01753', '0.085', '0.223', '-0.01846', '0.01349', '0.1774', '0.05478', '-0.572', '-0.0614', '0.4834']",,,,,,10067866,
mondo:0011906,congenital bile acid synthesis defect 1,"['congenital bile acid synthesis defect caused by mutation in HSD3B7', 'congenital bile acid synthesis defect, type 1', 'BASD1', '3-alpha beta-hydroxy-delta-5-C27-steroid oxidoreductase, deficiency of', 'bile acid synthesis defect, congenital, 1', 'HSD3B7 congenital bile acid synthesis defect', '3-Beta-hydroxy-Delta-5-C27-steroid oxidoreductase deficiency', 'CBAS1', 'congenital bile acid synthesis defect type 1', '3-beta-hydroxy-delta-5-C27-steroid oxidoreductase deficiency type 1', 'bile acid synthesis defect, congenital, type 1']",0111071,607765,79301,,"['-0.3635', '-0.3325', '-0.1447', '-0.1423', '0.2104', '-0.1098', '0.07214', '0.2333', '-0.2737', '0.413', '-0.6064', '-0.4268', '-0.0774', '0.3435', '-0.6074', '-0.91', '0.3406', '-0.446', '-0.04187', '-1.125', '0.3093', '-0.7554', '0.9946', '-0.02306', '0.1976', '-0.5566', '-0.0863', '-0.0556', '-0.0006814', '0.1609', '0.792', '0.4539', '-0.12134', '0.8726', '-0.01862', '-0.332', '-0.5776', '-0.1925', '0.4429', '0.404', '0.2612', '0.01431', '0.133', '0.3933', '-0.66', '-0.4028', '0.675', '-0.512', '-0.2025', '-0.3613', '-0.1104', '0.10223', '-0.1881', '-0.449', '-0.4482', '-0.2476', '0.09344', '-0.1473', '-0.5894', '0.1838', '0.4055', '0.2974', '0.3994', '-0.4058', '0.233', '-0.02701', '0.4885', '0.492', '-0.3257', '0.542', '-0.1921', '0.2107', '0.2766', '-0.10016', '0.793', '-0.2937', '0.3286', '-0.4927', '0.08795', '0.012245', '0.2705', '-0.2502', '-0.4475', '-0.4346', '-0.6094', '-0.1887', '0.1658', '0.11847', '0.2676', '-0.5327', '0.9937', '0.4592', '0.0677', '-0.2437', '0.682', '0.2092', '0.4758', '-0.3018', '-0.3843', '-0.1912']",,,C535442,,,,
mondo:0011907,acrocapitofemoral dysplasia,"['ACFD', 'acrocapitofemoral dysplasia']",0050604,607778,63446,C1843096,"['-0.568', '0.292', '-0.07733', '-0.19', '0.3975', '-0.575', '-0.357', '0.7173', '-0.7095', '-0.64', '-0.4067', '0.2151', '-0.1512', '-0.10034', '0.1566', '0.5317', '0.226', '-0.1249', '-0.4653', '-0.4744', '0.0371', '0.2019', '0.9014', '0.296', '0.4653', '0.2362', '-0.207', '0.0925', '-0.1571', '-0.1592', '0.387', '-0.7563', '0.03033', '0.2793', '0.4067', '-0.4792', '0.05365', '-0.3745', '0.2399', '-0.527', '-0.3909', '-0.4524', '0.0836', '0.01938', '-0.4126', '-0.1349', '0.02213', '0.256', '0.3499', '-0.716', '-0.1234', '-0.3398', '-0.5796', '0.07227', '-0.1073', '-0.8105', '0.1703', '-0.3965', '0.009315', '-0.0393', '0.0877', '-0.10223', '-0.4905', '0.1553', '-0.3525', '-0.11066', '-0.178', '0.666', '-0.2852', '-0.0485', '-0.3416', '-0.1998', '0.1891', '0.3594', '0.3186', '0.549', '-0.3564', '0.372', '-0.6084', '-0.5044', '0.3735', '0.2141', '-0.005642', '0.2617', '-0.1779', '0.348', '-0.007996', '0.2426', '0.10876', '-0.1351', '-0.3384', '0.2208', '-0.2096', '0.01706', '1.118', '0.2296', '0.4487', '-0.338', '0.2761', '-0.1449']",,,C564334,,,,
mondo:0011908,juvenile myelomonocytic leukemia,"['juvenile myelomonocytic leukemia, autosomal dominant, somatic mutation', 'juvenile chronic myelomonocytic leukaemia', 'JCML', 'juvenile chronic myeloid leukemia', 'leukemia, juvenile myelomonocytic', 'chronic myelomonocytic leukemia', 'juvenile chronic myelomonocytic leukemia', 'juvenile myelomonocytic leukemia', 'leukemia, juvenile myelomonocytic, somatic', 'juvenile chronic myelogenous leukemia', 'JMML', 'leukemia, chronic myelomonocytic', 'juvenile chronic myeloid leukaemia', 'juvenile chronic myelogenous leukaemia', 'chronic myelomonocytic leukaemia', 'leukemia, juvenile myelomonocytic, autosomal dominant, somatic mutation']",0050458,607785,86834,C0349639,"['0.5176', '0.04855', '-0.23', '0.10065', '-0.542', '-0.2656', '0.545', '0.9326', '0.2385', '-0.1621', '0.02496', '0.3066', '-0.05804', '0.4187', '-0.2788', '0.45', '-0.1819', '-0.2927', '-0.00564', '-0.2534', '0.0691', '-0.12463', '0.604', '-0.913', '0.3887', '-0.242', '-0.0852', '-0.5117', '-0.2886', '0.0634', '0.62', '0.3953', '0.574', '0.1814', '0.4678', '0.3674', '-1.477', '0.3018', '0.1855', '-0.5425', '-0.10077', '0.423', '-0.10223', '-0.02802', '-0.2477', '-0.1711', '0.0204', '-0.1735', '0.5747', '-0.6045', '0.3455', '0.1562', '0.2252', '-0.1996', '0.599', '0.1414', '-0.4646', '0.08936', '-0.5156', '-0.0786', '0.2306', '0.1813', '0.2076', '-0.3503', '-0.384', '-0.0637', '0.1636', '-0.1626', '-0.05002', '1.492', '-0.1333', '-0.10345', '-0.1776', '0.1135', '0.5312', '-0.05743', '-0.01596', '0.931', '-0.0832', '-0.4224', '-0.9146', '-0.4058', '-0.06125', '0.0665', '-0.6636', '-0.5537', '0.5957', '0.5156', '0.3384', '-0.1427', '0.1744', '-0.05103', '-0.621', '0.1072', '0.9424', '0.718', '-0.1277', '-0.8184', '-0.3677', '0.003767']",C9233,1000309,D054429,,,10023249,
mondo:0011909,Charcot-Marie-Tooth disease dominant intermediate D,"['autosomal dominant intermediate Charcot-Marie-Tooth disease type D', 'Charcot Marie Tooth disease dominant intermediate 3', 'MPZ Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth disease, dominant intermediate D', 'Di-Cmtd', 'Charcot-Marie-Tooth disease dominant intermediate type D', 'Charcot-Marie-Tooth disease caused by mutation in MPZ', 'CMTDID', 'Charcot-Marie-Tooth neuropathy, dominant Intermediate D', 'MPZ-related intermediate Charcot-Marie-Tooth neuropathy', 'Charcot-Marie-Tooth neuropathy dominant intermediate D', 'DI-CMTD', 'Charcot-Marie-Tooth disease, dominant Intermediate type D']",0110200,607791,100046,C1843075,"['0.368', '0.2786', '-2.7e-05', '-0.1571', '-0.11383', '0.1729', '-0.02121', '0.7905', '-0.7485', '-0.06064', '-0.1411', '0.309', '-0.4307', '0.5967', '-0.09143', '-0.1548', '-0.1299', '-0.5913', '-0.3982', '-0.5063', '0.1964', '0.2852', '0.0502', '0.9873', '0.39', '0.556', '0.011314', '0.0745', '0.16', '-0.1371', '0.2915', '-0.5645', '0.1918', '0.1444', '0.461', '-0.748', '-0.58', '-0.6104', '0.3215', '-0.11383', '-1.215', '-0.223', '-0.3179', '0.2961', '0.007072', '-0.0729', '-0.04312', '-0.09546', '-0.526', '-0.10364', '-0.08527', '0.06113', '-0.7275', '-0.8706', '0.1233', '-0.7144', '-0.123', '0.3345', '-0.6646', '-0.3633', '-0.1898', '0.2432', '0.758', '0.7534', '-1.104', '0.7983', '0.152', '0.9146', '-0.4104', '0.3413', '-0.6416', '0.1852', '0.3203', '-0.0911', '1.169', '0.8135', '-0.0866', '0.4524', '-0.0419', '-0.791', '0.0046', '-0.4004', '0.9707', '0.8203', '0.006058', '-0.0555', '0.10144', '0.8853', '1.012', '0.2487', '0.533', '-0.2404', '-0.2517', '0.3147', '0.74', '0.8374', '0.6865', '-0.6636', '-0.0348', '0.528']",,,C564333,,,,
mondo:0011911,craniolenticulosutural dysplasia,"['cranio-lenticulo-sutural dysplasia, CLSD', 'Boyadjiev-Jabs syndrome', 'CLSD', 'craniolenticulosutural dysplasia']",0070307,607812,50814,C1843042,"['-0.2081', '0.03027', '-0.1495', '-0.0867', '0.497', '-0.7427', '-0.337', '0.9385', '-0.773', '0.09485', '-0.1804', '0.161', '0.02084', '-0.2437', '-0.2225', '0.572', '0.788', '-0.256', '-0.263', '-0.4316', '0.12134', '0.0955', '0.254', '0.02435', '0.0789', '-0.1279', '-0.5854', '0.1807', '0.4612', '-0.2389', '0.7856', '-0.7256', '0.1812', '0.12396', '0.7886', '0.0986', '-0.372', '-0.4688', '0.149', '-0.6426', '0.553', '-0.2925', '-0.3735', '-0.0343', '0.1554', '0.1118', '0.0949', '0.0762', '-0.2155', '-0.7896', '0.551', '-0.002085', '0.08575', '0.3706', '-0.3354', '-0.87', '0.4358', '-0.1461', '0.342', '0.3137', '0.388', '-0.476', '-0.11664', '-0.226', '-0.3992', '0.4297', '0.4465', '0.6226', '-0.05148', '0.3306', '-0.3188', '0.3394', '-0.004322', '0.1078', '-0.6284', '-0.0541', '-0.407', '-0.2795', '-0.5205', '0.1377', '0.3306', '0.7275', '0.1416', '0.3354', '-0.1547', '-0.0201', '0.2196', '0.4485', '0.6943', '0.5044', '-0.286', '1.006', '-0.2185', '-0.0922', '0.6055', '-0.2815', '0.19', '-0.3955', '0.284', '0.2196']",,,C564332,,,,
mondo:0011912,autosomal recessive nonsyndromic hearing loss 37,"['deafness, autosomal recessive type 37', 'autosomal recessive deafness 37', 'deafness, autosomal recessive 37', 'autosomal recessive nonsyndromic deafness caused by mutation in MYO6', 'autosomal recessive nonsyndromic deafness 37', 'DFNB37', 'autosomal recessive nonsyndromic deafness type 37', 'MYO6 autosomal recessive nonsyndromic deafness']",0110495,607821,,C1843028,,,,C564331,,,,
mondo:0011913,Alzheimer disease 3,"['Alzheimer disease, familial, 3, with spastic paraparesis and apraxia', 'Alzheimer disease, type 3', 'Alzheimer disease, type 3, with spastic paraparesis and unusual plaques', 'Alzheimer disease 3, early-onset', 'AD', 'Alzheimer disease early onset type 3', 'familial Alzheimer^s disease, type 3', 'Alzheimer disease type 3', 'Alzheimer disease 3', 'early-onset autosomal dominant Alzheimer disease caused by mutation in PSEN1', 'familial Alzheimer disease, type 3', 'PSEN1 early-onset autosomal dominant Alzheimer disease', 'Alzheimer disease 3, early onset', 'Alzheimer disease, familial, 3, with spastic paraparesis and unusual plaques', 'Alzheimer disease familial 3', 'Alzheimer disease, protection against, due to APOE3-Christchurch', 'Alzheimer disease, type 3, with spastic paraparesis and apraxia', 'Alzheimer disease, familial, 3', 'Alzheimer^s disease type 3', 'Alzheimer^s disease 3', 'AD3']",0110042,607822,,,,C123412,,C536598,,,,
mondo:0011914,hypotrichosis-lymphedema-telangiectasia syndrome,"['HLTS', 'hypotrichosis-lymphedema-telangiectasia syndrome']",0111361,607823,,C1843004,,,,C564327,,,,
mondo:0011915,"mitral valve prolapse, myxomatous 2","['mitral valve prolapse 2', 'MMVP2', 'mitral valve prolapse, myxomatous 2', 'MVP2', 'myxomatous mitral valve prolapse 2']",,607829,,C1843003,,,,C564326,,,,
mondo:0011916,Charcot-Marie-Tooth disease axonal type 2K,"['CMT2K', 'autosomal recessive axonal CMT4C4', 'autosomal recessive Charcot-Marie-Tooth disease with hoarseness', 'autosomal recessive axonal Charcot-Marie-Tooth disease type 2K', 'Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2K', 'Charcot-Marie-Tooth neuropathy axonal type 2K', 'ARCMT2K', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2K', 'autosomal recessive axonal Charcot-Marie-Tooth disease disease type 2K', 'Charcot-Marie-Tooth neuropathy, axonal, type 2K', 'Charcot-Marie-Tooth disease, axonal, type 2K', 'Charcot-Marie-Tooth disease, autosomal dominant, type 2K']",0110167,607831,99944,C1842984,"['-0.01298', '0.3635', '-0.10046', '0.2031', '-0.10767', '-0.192', '0.01852', '0.645', '-0.4', '-0.4197', '-0.05627', '-0.04865', '-0.4353', '0.491', '-0.3918', '0.2047', '-0.09546', '-0.689', '-0.353', '-0.3293', '0.1969', '0.393', '0.2712', '0.566', '0.1575', '0.318', '0.228', '0.4714', '0.1602', '-0.48', '0.2527', '-0.4897', '0.282', '0.04337', '0.2625', '-0.788', '-0.65', '-0.4338', '0.2986', '-0.144', '-1.553', '-0.647', '-0.596', '0.2576', '0.08167', '0.0167', '0.407', '-0.2305', '-0.5713', '0.0947', '0.16', '0.3662', '-0.541', '-0.8774', '0.5513', '-0.427', '-0.437', '0.4417', '-0.2203', '0.08344', '0.02313', '-0.1819', '0.4934', '0.681', '-0.632', '1.08', '-0.11456', '0.6064', '-0.3896', '0.4016', '-0.634', '0.09094', '0.673', '0.0622', '0.8843', '0.8696', '-0.2426', '0.613', '0.117', '-0.4004', '-0.0902', '-0.3564', '0.838', '0.864', '0.12006', '-0.05713', '0.45', '0.4768', '0.536', '0.1776', '0.6055', '-0.008896', '0.147', '0.4316', '0.5674', '0.483', '0.245', '-0.6377', '0.0683', '0.3267']",,,,,,,
mondo:0011917,"focal segmental glomerulosclerosis 3, susceptibility to","['focal segmental glomerulosclerosis 3, susceptibility to', 'susceptibility to focal segmental glomerulosclerosis 3', 'CD2AP focal segmental glomerulosclerosis', 'glomerulosclerosis, focal segmental, 3', 'glomerulosclerosis, focal segmental, 3, susceptibility to', 'focal segmental glomerulosclerosis caused by mutation in CD2AP', 'FSGS3']",0112245,607832,,,,,,,,,,
mondo:0011918,anxiety,"['anxiety-related personality traits', 'harm avoidance', 'anxiety']",,607834,,,,,,D001007,,,,
mondo:0011919,"autoimmune disease, susceptibility to, 1","['AIS1', 'autoimmune disease caused by mutation in FOXD3', 'susceptibility to autoimmune disease 1', 'autoimmune disease, susceptibility to, type 1', 'autoimmune disease susceptibility locus, chromosome 1P-related', 'FOXD3 autoimmune disease', 'autoimmune disease, susceptibility to, 1', 'vitiligo-associated multiple autoimmune disease susceptibility 2']",,607836,,,,,,,,,,
mondo:0011920,autosomal dominant nonsyndromic hearing loss 48,"['MYO1A autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness 48', 'deafness, autosomal dominant type 48', 'autosomal dominant deafness 48', 'autosomal dominant nonsyndromic deafness caused by mutation in MYO1A', 'DFNA48', 'autosomal dominant nonsyndromic deafness type 48', 'deafness, autosomal dominant 48']",0110571,607841,,C1842939,,,,C564322,,,,
mondo:0011921,"aural atresia, congenital","['CAA', 'aural atresia, congenital, with hyposmia', 'aural atresia, congenital']",,607842,,C1842937,,,,C564321,,,,
mondo:0011922,nonimmune chronic idiopathic neutropenia of adults,"['adult idiopathic neutropenia', 'nonimmune chronic idiopathic neutropenia of adults', 'neutropenia, nonimmune chronic idiopathic, of adults', 'NI-CINA']",,607847,2688,C1842930,,,,C564320,,D70,,
mondo:0011923,osteoarthritis susceptibility 3,"['ASPN osteoarthritis', 'OS3', 'osteoarthritis of knee/hip', 'osteoarthritis caused by mutation in ASPN', 'osteoarthritis susceptibility 3', 'osteoarthritis susceptibility type 3']",,607850,,,,,,,,,,
mondo:0011924,panic disorder 2,"['Pand2', 'panic disorder 2', 'panic disorder susceptibility locus, chromosome 9Q-related', 'panic disorder type 2']",,607853,,C1842922,,,,,,,,
mondo:0011925,congenital merosin-deficient muscular dystrophy 1A,"['CMD1A', 'congenital merosin-deficient muscular dystrophy type 1A', 'muscular dystrophy, congenital merosin-deficient, type 1A', 'merosin-negative congenital muscular dystrophy', 'muscular dystrophy, congenital merosin-deficient, 1A', 'congenital muscular dystrophy caused by mutation in LAMA2', 'muscular dystrophy, congenital, due to partial LAMA2 deficiency', 'congenital muscular dystrophy due to laminin alpha2 deficiency', 'muscular dystrophy, congenital, merosin-deficient', 'muscular dystrophy, congenital merosin-deficient', 'LAMA2 congenital muscular dystrophy', 'LAMA2-related muscular dystrophy', 'muscular dystrophy, congenital, merosin deficient or partially deficient', 'merosin-deficient congenital muscular dystrophy', 'MDC1A', 'merosin-deficient congenital muscular dystrophy type 1A', 'congenital muscular dystrophy type 1A', 'laminin alpha-2 deficiency']",0110636,607855,258,C1263858,"['0.4033', '-0.541', '-0.6865', '-0.02504', '0.4414', '-1.089', '0.1628', '1.014', '-1.723', '-0.7373', '-0.2162', '0.0253', '-0.1151', '0.7256', '0.2256', '0.3743', '-0.527', '-0.6104', '-0.691', '-0.8433', '0.2301', '0.1219', '0.4666', '0.2847', '-0.08765', '-0.1525', '-0.325', '-0.5957', '0.1309', '-0.3584', '0.4854', '0.1321', '0.4373', '-0.1191', '0.04724', '0.0486', '-0.4158', '0.08813', '-0.2778', '-0.0475', '-0.06232', '-0.1847', '-0.44', '0.292', '0.04346', '0.2202', '0.1674', '0.402', '-0.377', '0.4827', '0.1775', '-0.256', '0.3152', '-0.7456', '0.4053', '-0.8223', '0.1746', '0.9766', '-0.2732', '0.2313', '0.25', '0.1654', '-0.03873', '0.3564', '-0.227', '0.05475', '-0.03162', '0.529', '-0.5186', '-0.2568', '-0.2063', '0.3635', '0.1257', '0.0804', '0.5605', '0.4907', '-0.00976', '0.1487', '-0.2507', '0.086', '0.505', '-0.2305', '-0.1125', '0.3154', '-0.4612', '0.3625', '-0.1638', '-0.2494', '0.5957', '0.263', '-0.248', '-0.0002768', '0.1016', '0.7', '-0.468', '-0.1727', '0.3599', '-0.605', '0.03085', '-0.1086']",C118783,0009138,,,,,
mondo:0011926,"psoriasis 9, susceptibility to","['psoriasis 9, susceptibility to', 'PSORS9', 'psoriasis susceptibility 9']",0111284,607857,,,,,,,,,,
mondo:0011927,tufted angioma,"['tufted angioma', 'tufted angioma (disease)', 'tufted hemangioma', 'angioma, tufted', 'tufted hemangioma of the skin', 'angioma tufted', 'tufted hemangioma of skin', 'angioblastoma of Nakagawa', 'tufted skin angioma', 'tufted angioma of skin', 'Nakagawa angioblastoma', 'tufted angioma of the skin']",,607859,1063,C0346073,,C4487,,C536924,215.9,,,0012329
mondo:0011928,caudal duplication,"['caudal DUPLICATION anomaly', 'dipygus', 'split notochord syndrome']",,607864,1756,C1842884,"['-0.1989', '0.1775', '0.1483', '-0.05374', '0.1997', '-0.05725', '0.03906', '0.003149', '-0.1405', '-0.1317', '-0.1993', '-0.03308', '-0.001644', '0.03235', '-0.1334', '-0.1239', '-0.06003', '-0.1753', '-0.01955', '-0.324', '0.01198', '0.07587', '0.4216', '-0.2249', '0.1398', '-0.02301', '-0.1418', '0.09546', '0.1245', '-0.1771', '0.1737', '-0.02094', '0.193', '0.1327', '0.0756', '-0.2106', '0.0703', '-0.10205', '-0.1412', '-0.2129', '0.010414', '-0.11456', '0.06287', '-0.2426', '-0.0671', '-0.1753', '0.004906', '0.0897', '-0.01516', '0.07526', '-0.02287', '-0.05356', '-0.0911', '0.02135', '-0.2303', '-0.1948', '0.1508', '-0.02133', '-0.2856', '0.187', '0.0478', '-0.01129', '-0.01454', '0.1742', '-0.05005', '-0.08075', '0.2017', '0.1346', '-0.299', '0.07605', '-0.1715', '0.1342', '0.2014', '0.01595', '-0.01804', '0.001805', '0.008316', '-0.0547', '-0.2045', '-0.3123', '0.0381', '0.02312', '0.08105', '0.3018', '-0.03162', '-0.1653', '0.03406', '0.1724', '0.0775', '-0.09515', '0.06033', '0.2482', '0.10986', '-0.0009594', '0.4453', '-0.1714', '0.3123', '-0.3123', '0.02069', '0.1368']",,,C564315,,,,
mondo:0011929,chromosome 1p36 deletion syndrome,"['chromosome 1p36 deletion syndrome, distal, isolated cases', 'deletion 1p36', 'monosomy 1P36 syndrome', 'chromosome 1p36 deletion syndrome', 'Del(1)(p36)', 'monosomy 1p36', 'monosomy 1pter', '1p36 deletion syndrome', 'subtelomeric 1p36 deletion', '1p36 microdeletion syndrome', '1p telomere deletion syndrome', 'deletion 1pter']",0060410,607872,1606,C1842870,,C74983,,C535362,758.39,,,
mondo:0011930,"epilepsy, familial adult myoclonic, 2","['epilepsy, familial adult myoclonic, type 2', 'benign adult familial myoclonic epilepsy 2', 'epilepsy, familial ADULT myoclonic, 2', 'cortical myoclonic tremor with epilepsy, familial, 2', 'ADRA2B epilepsy, familial adult myoclonic', 'cortical myoclonus and epilepsy, autosomal dominant', 'FAME2', 'epilepsy, familial adult myoclonic caused by mutation in ADRA2B', 'epilepsy, familial adult myoclonic, 2']",0111692,607876,,C1842852,,,,C564313,,,,
mondo:0011931,"ovarian cancer, susceptibility to, 1","['ovarian cancer, susceptibility to, 1', 'OVCAS1', 'ovarian cancer, susceptibility to']",,607893,,,,,,,,,,
mondo:0011932,hypotrichosis 6,"['hypotrichosis caused by mutation in DSG4', 'hypotrichosis 6', 'monilethrix-like hypotrichosis', 'HYPT6', 'autosomal recessive localized hypotrichosis', 'autosomal recessive localised hypotrichosis', 'DSG4 hypotrichosis', 'hypotrichosis type 6', 'hypotrichosis, localized, autosomal recessive', 'Htl', 'hypotrichosis, localized, autosomal recessive 1', 'Lah1']",0110703,607903,,C1842839,,,,C564312,,,,
mondo:0011933,ALG2-congenital disorder of glycosylation,"['CDG1I', 'mannosyltransferase 2 deficiency', 'congenital disorder of glycosylation type Ii', 'ALG2-CDG (CDG-II)', 'carbohydrate-deficient glycoprotein syndrome type 1I', 'congenital disorder of glycosylation type 1i', 'ALG2-CDG', 'CDG syndrome type Ii', 'CDG 1I', 'CDG Ii', 'congenital disorder of glycosylation, type Ii', 'carbohydrate deficient glycoprotein syndrome type Ii']",0080561,607906,79326,,"['-0.1448', '0.1715', '0.276', '-0.02324', '0.1439', '-0.2036', '-0.0929', '0.1431', '-0.2495', '-0.2578', '-0.147', '-0.1849', '-0.0823', '-0.2378', '-0.04102', '0.1525', '0.1388', '-0.1909', '-0.0788', '-0.4666', '0.005924', '-0.0693', '-0.0726', '0.004574', '0.0938', '0.1493', '-0.1647', '-0.02737', '0.301', '-0.1385', '0.152', '0.3052', '0.3818', '0.10675', '-0.1741', '-0.0659', '0.1225', '-0.2986', '-0.1393', '-0.3513', '0.1005', '-0.2725', '0.1252', '0.0698', '-0.1425', '-0.262', '0.0544', '0.322', '0.3567', '0.1335', '-0.04935', '-0.0502', '0.03326', '-0.05682', '-0.0754', '-0.2766', '0.3445', '0.2898', '-0.3855', '0.2034', '0.1218', '-0.00902', '0.3325', '0.02844', '-0.01706', '-0.1626', '0.195', '0.1741', '-0.2422', '0.0854', '-0.342', '0.0986', '0.0963', '0.09454', '0.1299', '0.2167', '0.358', '0.05615', '-0.3032', '0.1722', '0.08264', '0.1081', '-0.0713', '0.2275', '0.1934', '0.08704', '0.2373', '0.488', '0.208', '0.3796', '0.01562', '0.506', '0.0631', '-0.1483', '0.498', '0.242', '0.4792', '-0.3599', '0.1604', '0.1759']",,,,,,,
mondo:0011934,dermatofibrosarcoma protuberans,"['dermatofibrosarcoma', 'metastatic dermatofibrosarcoma protuberans (subtype)', 'dermatofibrosarcoma protuberans', 'giant cell fibroblastoma', 'DFSP', 'familial dermatofibrosarcoma protuberans (subtype)']",3507,607907,31112,C0392784,"['-0.10913', '0.2913', '-0.0571', '0.0334', '0.11365', '-0.0621', '0.7573', '0.169', '-0.3167', '-0.603', '0.1926', '0.5454', '-0.274', '0.05515', '-0.2952', '0.05276', '0.005066', '-0.626', '0.4333', '-0.53', '-0.5435', '-0.2827', '0.653', '-0.407', '0.0802', '0.0814', '0.033', '-0.11304', '-0.7554', '-0.04465', '0.812', '-0.115', '0.1428', '-0.4102', '-0.2003', '0.4465', '-0.3293', '0.683', '-0.1769', '-0.1664', '0.259', '-0.1302', '-0.2583', '-0.591', '0.3506', '-0.11017', '-0.2898', '-0.5415', '0.5376', '-0.92', '0.2927', '0.002531', '0.4607', '-0.354', '-0.01556', '0.1213', '-0.3813', '0.3525', '-0.1462', '-0.1691', '0.3394', '0.511', '-0.653', '-0.1942', '-0.10504', '0.1423', '0.7925', '0.08923', '0.1255', '0.7705', '-0.465', '0.4146', '-0.1464', '-0.1747', '0.8735', '0.403', '0.03265', '0.3552', '-0.2092', '-0.601', '-0.7075', '0.03146', '0.2184', '-0.0529', '-0.746', '-0.356', '0.3115', '0.3406', '0.3765', '-0.02707', '0.04977', '-0.11633', '-0.4856', '-0.2473', '0.4514', '-0.1458', '0.014496', '-0.7324', '-0.303', '-0.4014']",C4683,,D018223,,,10057070,
mondo:0011935,retinitis pigmentosa 30,"['RP30', 'RP 30', 'retinitis pigmentosa 30', 'macular Degeneration', 'retinitis pigmentosa type 30', 'FSCN2 retinitis pigmentosa', 'retinitis pigmentosa caused by mutation in FSCN2']",0110406,607921,,C1842816,,,,,,H35.5,,
mondo:0011936,microphthalmia with brain and digit anomalies,"['anophthalmia, clinical, with micrognathia, malformed ears, digital anomalies, and abnormal external genitalia', 'anophthalmia clinical with micrognathia malformed ears digital anomalies and abnormal external genitalia', 'syndromic microphthalmia type 6', 'microphthalmia with brain and digit developmental anomalies', 'microphthalmia syndromic 6', 'microphthalmia, syndromic type 6', 'Bakrania-Ragge syndrome', 'microphthalmia and pituitary anomalies', 'microphthalmia, syndromic 6', 'MCOPS6']",0111805,607932,139471,C4303070,"['-0.1425', '-0.1637', '0.117', '0.1398', '0.1624', '-0.2235', '-0.087', '0.005672', '-0.2112', '-0.3584', '-0.3672', '-0.2327', '0.05478', '-0.1445', '0.00931', '-0.395', '0.2754', '-0.38', '-0.4268', '-0.4763', '0.0829', '0.09', '0.1278', '-0.3743', '0.1681', '-0.151', '-0.1957', '0.2954', '-0.01819', '-0.2227', '0.3337', '-0.1892', '0.3708', '0.04617', '0.1915', '-0.02736', '0.4785', '-0.1868', '0.013115', '-0.0706', '0.3848', '0.001192', '-0.2258', '-0.3357', '-0.02695', '-0.1509', '0.281', '0.0543', '-0.4233', '-0.3054', '-0.02771', '-0.3523', '0.0804', '0.2294', '0.1885', '-0.1768', '0.3728', '0.0241', '-0.311', '0.407', '0.1803', '-0.03117', '0.2041', '0.2766', '-0.4019', '-0.0246', '0.3184', '0.3865', '-0.4731', '0.233', '-0.318', '0.3252', '0.0613', '0.04807', '0.35', '-0.03778', '0.2659', '0.2192', '-0.09753', '-0.0519', '0.1749', '0.3726', '0.343', '0.8647', '-0.1254', '-0.3237', '0.1605', '0.5605', '-0.01396', '0.2722', '-0.005184', '0.4492', '-0.0727', '0.03174', '0.447', '-0.095', '0.2361', '-0.2783', '0.2644', '-0.03058']",,,C566440,,,,
mondo:0011937,peeling skin syndrome 4,"['peeling skin syndrome caused by mutation in CSTA', 'ichthyosis, exfoliative, autosomal recessive', 'CSTA peeling skin syndrome', 'PSS4', 'peeling skin syndrome 4', 'peeling skin syndrome type 4', 'ichthyosis bullosa of Siemens-like']",,607936,,C4225407,,,,C564309,,,,
mondo:0011938,atrial septal defect 2,"['GATA4 atrial heart septal defect', 'atrial septal defect 2', 'atrial heart septal defect type 2', 'atrial heart septal defect caused by mutation in GATA4', 'atrial septal defect type 2', 'ASD2']",0110107,607941,,C1842778,,,,C538263,,,,
mondo:0011939,Spondyloenchondrodysplasia with immune dysregulation,"['SEM', 'SPENCD', 'SPENCDI', 'spondyloenchondromatosis', 'spondylometaphyseal dysplasia with combined immunodeficiency', 'Roifman Immunoskeletal syndrome', 'spondylometaphyseal dysplasia with enchondromatous changes', 'spondyloenchondrodysplasia', 'combined immunodeficiency with autoimmunity and spondylometaphyseal dysplasia', 'spondyloenchondrodysplasia with immune dysregulation']",,607944,50816,C1842763,"['-0.2844', '0.2054', '0.368', '-0.3782', '0.1432', '-0.05624', '-0.07806', '-0.1476', '-0.04105', '-0.0903', '-0.01558', '0.005142', '0.10016', '-0.15', '-0.03375', '-0.09485', '0.01686', '0.03378', '-0.205', '-0.557', '0.1759', '-0.03592', '0.436', '-0.2426', '-0.07336', '0.1088', '-0.05035', '-0.1465', '0.2434', '-0.296', '0.0738', '-0.03314', '0.553', '0.2546', '0.2937', '-0.1406', '-0.3396', '-0.394', '-0.2637', '-0.2617', '-0.04413', '-0.3174', '0.02875', '-0.445', '0.2455', '-0.309', '0.03946', '0.556', '0.1058', '0.09845', '0.03482', '0.3552', '0.08765', '0.1295', '-0.2189', '-0.3945', '-0.362', '-0.2588', '-0.3235', '0.1163', '0.35', '-0.02968', '-0.3806', '0.02121', '0.010376', '-0.1135', '0.362', '0.2932', '-0.3901', '0.3618', '-0.1362', '-0.353', '0.09534', '-0.0797', '-0.003885', '0.1666', '0.1274', '-0.01473', '0.10406', '-0.1622', '-0.05298', '-0.07574', '-0.0951', '0.0962', '-0.06494', '0.0189', '0.0617', '0.01085', '0.2563', '-0.02419', '0.4412', '-0.01448', '0.2139', '-0.06506', '0.3232', '0.3564', '0.49', '0.1917', '0.2722', '0.1843']",,0002326,C564307,759.89,,,
mondo:0011940,"mycobacterium tuberculosis, susceptibility to","['tuberculosis, protection against', 'tuberculosis, susceptibility to', 'tuberculosis infection, protection against', 'Mycobacterium tuberculosis, susceptibility to infection by', 'mycobacterium tuberculosis, susceptibility to', 'Mycobacterium tuberculosis, protection against']",,607948,,,,,,C536092,,,,
mondo:0011941,"mycobacterium tuberculosis, susceptibility to, 1","['mycobacterium tuberculosis, susceptibility to, 1', 'MTBS1', 'Mycobacterium tuberculosis, susceptibility to, type 1', 'tuberculosis, susceptibility to']",,607949,,,,,,,,,,
mondo:0011942,"systemic lupus erythematosus with nephritis, susceptibility to, 1","['SLEN1', 'systemic lupus erythematosus with nephritis, susceptibility to, 1']",,607965,,,,,,,,,,
mondo:0011943,"systemic lupus erythematosus with nephritis, susceptibility to, 2","['SLEN2', 'systemic lupus erythematosus with nephritis, susceptibility to, 2']",,607966,,,,,,,,,,
mondo:0011944,"systemic lupus erythematosus with nephritis, susceptibility to, 3","['systemic lupus erythematosus with nephritis, susceptibility to, 3', 'SLEN3']",,607967,,,,,,,,,,
mondo:0011945,Gaucher disease perinatal lethal,"['Gaucher disease perinatal lethal', 'Gaucher disease, collodion type', 'perinatal lethal Gaucher disease', 'Gaucher disease collodion type', 'Gaucher disease, perinatal lethal', 'Gaucher disease, perinatal-lethal form', 'Gaucher^s disease perinatal lethal', 'fetal Gaucher disease', 'foetal Gaucher disease']",0110960,608013,85212,C1842704,"['-0.3625', '0.819', '0.1556', '-0.688', '-0.16', '-0.5034', '-0.2284', '0.85', '-1.078', '-0.4553', '-0.2847', '0.03302', '-0.06805', '0.893', '0.2642', '-0.4224', '-0.07446', '0.4177', '-0.453', '-0.844', '-0.735', '-0.6265', '0.6997', '-0.538', '-0.0959', '-0.03375', '-0.1425', '0.4624', '0.5894', '-0.3293', '0.3828', '0.1683', '0.5137', '0.017', '0.10895', '0.11523', '-0.6685', '-0.4863', '0.1412', '-0.07684', '0.2102', '-0.2507', '-0.4512', '-0.4868', '-0.517', '0.02771', '-0.3584', '-0.1222', '-0.01298', '0.232', '0.3718', '0.1759', '0.9253', '-0.3608', '0.2435', '-0.3384', '-0.4749', '0.11273', '0.4521', '-0.2903', '-0.12195', '-0.364', '0.395', '-0.95', '-0.359', '0.09515', '0.1721', '-0.10785', '-1.108', '-0.02034', '0.1815', '0.2266', '0.1266', '-0.01553', '0.3872', '-0.005077', '-0.05423', '0.5654', '-0.1992', '-0.6143', '-0.3796', '-0.665', '-0.0805', '-0.4001', '-0.6143', '-0.612', '0.8545', '0.1025', '0.346', '0.2036', '0.02556', '-0.2311', '0.3962', '0.486', '0.571', '1.321', '-0.0929', '-0.2242', '0.77', '-1.226']",,,C564306,,,,
mondo:0011946,diaphanospondylodysostosis,"['vertebral ossification, defect in, with nephrogenic rests', 'diaphanospondylodysostosis']",,608022,66637,C1842691,"['-0.2318', '0.1783', '0.008385', '-0.2102', '0.1715', '-0.0648', '-0.4348', '0.519', '-0.446', '-0.919', '-0.1426', '-0.3572', '-0.6006', '0.2234', '-0.1006', '0.2317', '0.05243', '0.08234', '-0.3982', '-0.5615', '-0.0481', '0.02876', '0.884', '-0.293', '0.192', '-0.1208', '-0.4675', '0.11285', '0.4998', '-0.4963', '0.3464', '-0.563', '0.07227', '0.544', '0.4268', '-0.311', '-0.2898', '-0.3684', '0.2455', '-0.01741', '-0.1503', '0.05573', '-0.1117', '-0.526', '-0.01593', '-0.5684', '0.1242', '0.4744', '-0.2043', '-0.0363', '0.2385', '-0.1652', '-0.1125', '0.203', '-0.1255', '-0.5776', '-0.06506', '-0.05374', '0.2296', '0.2522', '0.3677', '0.1506', '-0.3787', '0.312', '-0.1439', '-0.203', '0.531', '0.4321', '-0.6636', '0.2266', '0.1791', '0.3616', '0.251', '-0.1687', '-0.3647', '0.2211', '0.11633', '0.0619', '-0.1279', '-0.1014', '-0.4968', '0.6357', '0.3894', '0.2368', '-0.306', '0.3079', '0.11163', '-0.1209', '-0.2103', '-0.1655', '-0.3704', '-0.1686', '-0.2678', '0.1376', '0.8057', '0.07806', '0.218', '-0.0145', '0.08575', '0.1362']",,,C564305,,,,
mondo:0011948,pontocerebellar hypoplasia type 3,"['PCH with optic atrophy', 'non-syndromic pontocerebellar hypoplasia caused by mutation in PCLO', 'Pch with optic atrophy', 'PCH without dyskinesia', 'cerebellar atrophy with progressive microcephaly', 'PCLO non-syndromic pontocerebellar hypoplasia', 'PCH3', 'clam', 'pontocerebellar hypoplasia, type 3']",0060272,608027,97249,C1842687,"['0.1481', '0.532', '-0.139', '-0.1544', '0.234', '-0.5537', '-0.311', '0.8745', '-0.762', '-0.3967', '-0.3247', '-0.5044', '-0.5967', '-0.2837', '0.345', '0.8022', '0.2915', '-0.4907', '0.147', '-1.228', '-0.1434', '-0.4026', '0.5874', '-0.03336', '0.015396', '0.2014', '-0.3223', '0.2327', '0.011665', '-0.4438', '0.656', '0.244', '-0.021', '0.164', '-0.263', '0.3477', '-0.2798', '0.3184', '-0.377', '0.02835', '0.1593', '-0.6816', '-0.0675', '-0.0734', '-0.282', '-0.44', '0.1268', '-0.01932', '-0.1056', '-0.273', '0.2273', '-0.1201', '-0.399', '-0.1685', '0.3472', '-0.6953', '0.1323', '-0.3328', '-0.007576', '0.724', '-0.6206', '-0.3127', '0.4473', '0.323', '-1.019', '0.00798', '0.584', '0.113', '-0.3357', '0.8433', '-0.866', '0.2688', '0.2225', '0.1404', '0.7246', '0.02684', '0.09485', '-0.2109', '-0.6895', '0.115', '0.3171', '0.3584', '0.7427', '0.825', '-0.2847', '0.2935', '-0.134', '0.912', '0.7207', '0.0813', '-0.4297', '0.548', '0.1681', '-0.19', '0.3733', '0.654', '0.1042', '0.1669', '0.5815', '-0.01105']",,,C548072,,,,
mondo:0011949,Thai symphalangism syndrome,['Thai symphalangism syndrome'],,608028,,C1842679,,,,C564303,,,,
mondo:0011950,infantile-onset autosomal recessive nonprogressive cerebellar ataxia,"['autosomal recessive spinocerebellar ataxia type 6', 'SCAR6', 'cerebellar ataxia, infantile nonprogressive, autosomal recessive', 'cerebellar ataxia infantile nonprogressive autosomal recessive', 'Norwegian infantile onset ataxia', 'spinocerebellar ataxia, autosomal recessive 6', 'spinocerebellar ataxia autosomal recessive 6']",0111617,608029,284332,C1842676,"['-0.1685', '-0.2148', '0.0638', '0.03806', '-0.298', '-0.964', '0.1573', '0.04892', '-0.613', '-0.856', '-0.02832', '0.295', '-0.1777', '0.1139', '0.4827', '-0.2578', '-0.2017', '-0.3093', '-0.02753', '-0.9526', '-0.05463', '-0.1733', '0.2294', '-0.6704', '0.592', '-0.4055', '-0.2317', '0.1951', '-0.1226', '-0.96', '-0.05197', '0.3523', '-0.514', '-0.081', '0.3892', '0.03464', '-0.2107', '0.2003', '0.58', '0.2137', '0.3425', '0.317', '-0.4631', '0.4949', '0.6216', '-0.6973', '0.1495', '0.4631', '0.466', '-0.0243', '-0.03102', '0.326', '-0.3477', '-0.437', '-0.1255', '-0.8076', '0.4155', '0.544', '-0.1986', '0.565', '-0.536', '0.2493', '0.2201', '-0.1191', '-0.4326', '0.6196', '0.2725', '0.6606', '-0.62', '0.4785', '0.9634', '0.625', '-0.0345', '-0.883', '0.947', '0.2325', '0.2622', '0.3362', '0.2137', '0.5337', '-0.4214', '-0.832', '0.3152', '0.8354', '-0.275', '-0.6196', '0.1271', '-0.09894', '0.444', '0.4883', '0.396', '0.5576', '-0.094', '0.0832', '0.9907', '1.037', '0.4275', '0.5186', '-0.3574', '-0.02924']",,,C537312,,,,
mondo:0011951,amyotrophic lateral sclerosis type 6,"['amyotrophic lateral sclerosis 6, with or without frontotemporal dementia', 'amyotrophic lateral sclerosis caused by mutation in FUS', 'amyotrophic lateral sclerosis 6 with or without frontotemporal dementia', 'FUS amyotrophic lateral sclerosis', 'autosomal recessive amyotrophic lateral sclerosis 6', 'ALS6']",0060198,608030,,,,,,C567699,,,,
mondo:0011952,amyotrophic lateral sclerosis type 7,"['ALS7', 'amyotrophic lateral sclerosis 7']",0060199,608031,,C1842674,,,,C564300,,,,
mondo:0011953,familial acute necrotizing encephalopathy,"['susceptibility to acute necrotizing encephalopathy', 'susceptibility to infection-induced acute encephalopathy 3', 'encephalopathy, acute, infection-induced, susceptibility to, 3', 'encephalopathy, acute, infection-induced, 3, susceptibility to', 'encephalopathy, acute necrotizing, susceptibility to', 'recurrent acute necrotizing encephalopathy', 'ADANE', 'Postinfectious acute necrotizing hemorrhagic encephalopathy', 'encephalopathy, acute, infection-induced, susceptibility to, type 3', 'susceptibility to acute infection-induced encephalopathy-3', 'IIAE3', 'infection-induced acute encephalopathy 3', 'ANE1', 'acute necrotizing encephalopathy type 1', 'autosomal dominant acute necrotizing encephalopathy']",,608033,88619,C4509836,"['-0.5137', '0.3413', '-0.4343', '-0.27', '-0.4216', '-1.003', '0.2242', '0.2134', '-0.6133', '0.10815', '-0.736', '-0.3035', '0.1208', '-0.3967', '0.4263', '0.4038', '-0.11676', '0.04507', '0.01501', '-1.002', '0.1417', '0.24', '0.1266', '-0.7544', '0.03323', '-0.1743', '0.1508', '0.428', '-0.949', '-0.3196', '0.0945', '-0.02734', '0.253', '-0.2754', '0.0532', '0.191', '0.01396', '-0.4287', '-0.368', '-0.004353', '0.3442', '-0.29', '0.2874', '-0.02676', '0.2028', '-0.1148', '-0.4028', '-0.3613', '-0.8076', '0.2656', '0.0634', '0.582', '0.05646', '0.4067', '0.6255', '-0.7363', '0.3916', '0.2776', '-0.07367', '0.4822', '0.0627', '-0.2195', '0.4214', '0.2014', '-0.6016', '0.0721', '0.623', '0.284', '-0.1355', '0.6616', '-0.2296', '0.4448', '-0.2484', '-0.00982', '-0.1118', '0.202', '-0.223', '0.788', '-0.237', '0.01301', '-0.2703', '0.2026', '0.10724', '0.3635', '0.8', '-0.1862', '0.4634', '0.4763', '0.1511', '-0.0014', '0.4326', '0.3904', '-0.2834', '0.1997', '0.6436', '0.3936', '0.0951', '-0.4885', '0.4648', '-0.01965']",,,,,,,
mondo:0011954,"melanoma, cutaneous malignant, susceptibility to, 4","['melanoma, cutaneous malignant, 4', 'melanoma, cutaneous malignant, susceptibility to, 4', 'CMM4']",,608035,,,,,,,,,,
mondo:0011955,"diabetes mellitus, noninsulin-dependent, 4","['noninsulin-dependent diabetes mellitus 4', 'diabetes mellitus, noninsulin-dependent, 4', 'Niddm4', 'diabetes mellitus, noninsulin-dependent, type 4']",,608036,,C1842642,,,,C564299,,,,
mondo:0011956,"autism, susceptibility to, 3","['autism susceptibility 3, isolated cases', 'autism, susceptibility to, 3', 'AUTS3']",,608049,,,,,,,,,,
mondo:0011957,retinal macular dystrophy type 2,"['macular dystrophy, retinal, 2', 'macular dystrophy, retinal, type 2', 'MCDR2']",,608051,319640,,"['-0.2339', '-0.385', '0.221', '-0.1736', '0.00961', '-0.3826', '-0.05353', '0.04956', '-0.2067', '-0.3013', '-0.1046', '-0.2412', '-0.5024', '-0.1353', '-0.05075', '-0.3645', '0.397', '0.2761', '0.1619', '-0.4233', '-0.2335', '-0.005417', '0.1459', '0.3525', '-0.1604', '-0.1356', '-0.2651', '-0.3655', '-0.1272', '0.11743', '0.4595', '-0.0609', '0.2524', '0.1061', '0.1508', '0.3127', '-0.11804', '-0.1534', '-0.02448', '-0.365', '0.637', '0.00285', '0.1915', '-0.02196', '-0.3281', '0.11237', '-0.05322', '-0.1764', '-0.262', '0.11804', '0.3557', '0.2637', '0.2399', '-0.3425', '-0.2338', '-0.04916', '0.5625', '-0.2556', '-0.2756', '-0.0899', '0.1586', '-0.1581', '0.1398', '0.006847', '0.1428', '-0.10223', '0.5728', '0.44', '-0.3142', '0.3325', '-0.2421', '-0.1356', '0.02708', '-0.003498', '0.4082', '0.03915', '0.01945', '0.2177', '-0.202', '-0.1788', '0.2551', '-0.2494', '0.2228', '0.6274', '-0.4058', '-0.282', '0.0832', '-0.1004', '0.1714', '-0.02469', '0.1377', '0.2773', '0.1792', '0.2976', '0.7495', '0.4602', '0.3845', '-0.389', '-0.0731', '0.1503']",,,C562746,,H35.5,,
mondo:0011958,"bile and pancreatic ducts, complete absence of","['bile and pancreatic ducts, complete absence of']",,608063,,,,,,C564298,,,,
mondo:0011959,sweet syndrome,"['Gomm-button disease', 'acute febrile neutrophilic dermatosis', 'neutrophilic dermatosis, acute febrile', 'Afnd', 'sweet syndrome', 'Gomm button disease']",0080746,608068,3243,C0085077,,C85177,,D016463,702.8,,10000748,
mondo:0011960,schizophrenia 11,"['schizophrenia 11', 'schizophrenia susceptibility locus, chromosome 10Q-related', 'SCZD11', 'schizophrenia type 11', 'Sczd11']",0070087,608078,,C1842605,,,,,,,,
mondo:0011961,hereditary sensory and autonomic neuropathy type 1B,"['hereditary sensory and autonomic neuropathy type 1 with cough and gastroesophageal reflux', 'neuropathy, hereditary sensory and autonomic, type 1B', 'neuropathy, hereditary sensory and autonomic, type I, with cough and gastroesophageal reflux', 'hereditary sensory and autonomic neuropathy type IB', 'hereditary sensory neuropathy type 1B', 'neuropathy, hereditary sensory, type 1B', 'neuropathy, hereditary sensory, type IB', 'HSAN with cough and gastroesophageal reflux', 'HSAN1B', 'hereditary sensory neuropathy type IB']",0070148,608088,139564,C4303567,,,,C564296,,,,
mondo:0011962,endometrial cancer,"['endometrial cancer', 'endometrial cancer, familial, autosomal dominant, somatic mutation', 'malignant neoplasm of endometrium', 'tumour of endometrium', 'endometrium cancer', 'tumor of endometrium', 'endometrial neoplasm', 'primary malignant neoplasm of endometrium', 'cancer of endometrium', 'malignant endometrium neoplasm', 'endometrial Ca', 'endometrial carcinoma, somatic', 'malignant endometrial neoplasm', 'endometrial cancer, susceptibility to, autosomal dominant, somatic mutation', 'neoplasm of endometrium']",1380,608089,,,"['0.01657', '0.04413', '-0.02873', '-0.00717', '0.012856', '-0.0633', '0.02672', '0.0531', '-0.03232', '-0.03983', '0.00454', '0.02548', '0.01336', '0.01477', '-0.0412', '-0.0737', '-0.007366', '-0.01662', '-0.01407', '-0.088', '-0.012535', '-0.02888', '0.02982', '-0.04385', '0.05853', '-0.0358', '-0.0002573', '-0.0002906', '-0.02011', '-0.057', '0.04858', '-0.01582', '0.06793', '-0.013054', '0.02689', '-0.0132', '-0.0341', '-0.01595', '0.00953', '-0.02333', '0.00949', '-0.0538', '0.02411', '-0.05466', '0.00686', '-0.0305', '0.001051', '0.03772', '0.04193', '0.01498', '-0.01819', '0.01015', '0.00467', '0.02377', '-0.04117', '-0.001856', '0.0365', '-0.01478', '-0.08905', '-0.02885', '0.05637', '0.01079', '0.02495', '0.02928', '0.01143', '0.0462', '0.08075', '0.03482', '-0.03778', '0.0569', '-0.02795', '-0.001779', '-0.001952', '-0.02203', '0.04913', '0.006172', '-0.009834', '-0.00367', '-0.03378', '-0.05356', '-0.05014', '0.01212', '-0.02544', '0.01718', '-0.02992', '-0.02808', '0.02382', '0.04504', '0.082', '-0.00844', '-0.00573', '0.06525', '-0.00939', '-0.008286', '0.096', '0.02785', '0.03522', '-0.06995', '-0.0356', '0.01726']",C27815,0004230,,,,,
mondo:0011963,Joubert syndrome 2,"['cerebellooculorenal syndrome 2', 'Joubert syndrome type 2', 'Joubert syndrome caused by mutation in TMEM216', 'Cerebellooculorenal syndrome 2', 'Joubert syndrome 2', 'CORS2', 'TMEM216 Joubert syndrome', 'JBTS2']",0110988,608091,,C1842577,,,,C536294,,,,
mondo:0011964,DPAGT1-congenital disorder of glycosylation,"['dolichyl-phosphate N-acetylgalactosamine phosphotransferase deficiency', 'CDG 1J', 'carbohydrate deficient glycoprotein syndrome type Ij', 'congenital disorder of glycosylation type 1j', 'DPAGT1-CDG', 'CDGIj', 'DPAGT1-CDG (CDG-Ij)', 'CDG syndrome type Ij', 'congenital disorder of glycosylation, type Ij', 'congenital disorder of glycosylation type Ij', 'CDG-Ij', 'CDG1J', 'CDG Ij']",0080562,608093,86309,C2931004,"['-0.505', '0.0689', '0.292', '-0.3916', '0.2239', '-0.557', '0.01261', '0.3386', '-0.7236', '-0.5454', '-0.2206', '-0.186', '-0.02948', '-0.175', '-0.09314', '0.3564', '0.272', '-0.0516', '-0.3928', '-0.431', '0.2415', '0.004547', '0.0501', '-0.0463', '0.296', '0.1986', '0.0895', '0.0942', '0.332', '-0.324', '0.0694', '0.1946', '0.5586', '0.2986', '-0.05222', '-0.02719', '-0.03265', '-0.07196', '-0.2396', '-0.2069', '-0.1407', '-0.3533', '-0.00858', '0.3455', '-0.2206', '0.00821', '0.2102', '0.24', '0.2144', '0.3628', '-0.4985', '-0.02382', '-0.10095', '0.2308', '-0.256', '-0.3328', '0.3008', '0.0881', '-0.10645', '0.394', '0.4119', '0.0847', '0.1661', '-0.0006514', '0.0349', '-0.04272', '0.1908', '0.0962', '-0.3467', '0.1667', '-0.4675', '0.4094', '0.3132', '0.11847', '-0.0932', '0.1328', '0.638', '-0.1262', '-0.4438', '0.3167', '0.2306', '0.12286', '0.1055', '0.4194', '0.00632', '0.1525', '-0.08734', '0.7085', '0.2932', '0.2206', '-0.07385', '0.5225', '0.001191', '-0.000985', '0.2401', '0.415', '0.661', '-0.1437', '0.4026', '0.2942']",C126874,,C535748,,,,
mondo:0011965,familial temporal lobe epilepsy 2,"['familial temporal lobe epilepsy', 'Ftle', 'familial temporal lobe epilepsy type 2', 'epilepsy, familial temporal lobe', 'epilepsy, familial temporal lobe, 2', 'ETL2', 'temporal epilepsy, familial']",0060755,608096,98819,,,,,C536956,,,,
mondo:0011966,"periventricular heterotopia with microcephaly, autosomal recessive","['periventricular heterotopia with microcephaly, autosomal recessive', 'periventricular nodular heterotopia 2', 'heterotopia, periventricular, autosomal recessive', 'ARPHM']",,608097,,C1842563,,,,C564292,,,,
mondo:0011967,"heterotopia, periventricular, associated with chromosome 5P anomalies","['heterotopia, periventricular, associated with chromosome 5P anomalies', 'periventricular nodular heterotopia 3']",,608098,,C1842562,,,,C564291,,,,
mondo:0011968,autosomal recessive limb-girdle muscular dystrophy type 2D,"['autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCA', 'limb-girdle muscular dystrophy due to alpha-sarcoglycan deficiency', 'limb-girdle muscular dystrophy type 2D', 'SGCA autosomal recessive limb-girdle muscular dystrophy', 'Duchenne-like autosomal recessive muscular dystrophy type 2', 'Adhalinopathy, primary', 'muscular dystrophy, limb-girdle, autosomal recessive 3', 'limb-girdle muscular dystrophy, type 2D', 'muscular dystrophy, limb-girdle, type 2D', 'muscular dystrophy limb-girdle with alpha-sarcoglycan', 'Alpha-sarcoglycanopathy', 'primary adhalinopathy', 'Duchenne-like autosomal recessive muscular dystrophy, type 2', 'LGMD2D', 'DMDA2']",0110278,608099,62,,"['-0.28', '-0.7495', '-0.4126', '-0.3262', '0.09436', '-1.282', '0.2345', '0.551', '-1.758', '-0.9697', '0.05176', '0.329', '-0.2903', '1.226', '0.4248', '0.3098', '-0.7993', '-0.431', '-0.3777', '-0.6494', '-0.136', '0.1426', '0.5527', '0.426', '0.2595', '-0.3628', '-0.0206', '-0.774', '0.03784', '-0.3706', '0.7695', '0.1611', '0.801', '0.02458', '0.15', '0.007557', '-0.538', '0.1564', '0.3503', '-0.5127', '-0.0697', '-0.615', '-0.6377', '0.6045', '-0.14', '0.2169', '-0.1941', '0.6846', '-0.119', '0.5337', '0.4668', '-0.3467', '0.4287', '-0.853', '0.358', '-0.4326', '0.495', '0.9077', '-0.2861', '0.1121', '0.0938', '0.04184', '0.0003166', '-0.09973', '-0.1307', '-0.1416', '0.07837', '0.53', '-0.4326', '-0.0652', '-0.2253', '0.09045', '0.1147', '-0.0564', '0.9966', '0.617', '-0.2305', '0.0592', '-0.1442', '0.0759', '0.2025', '-0.453', '-0.01175', '0.0919', '-0.2174', '0.2433', '-0.1666', '-0.526', '0.838', '0.337', '-0.669', '-0.04614', '0.11475', '0.788', '-0.1691', '0.404', '0.426', '-0.361', '0.0489', '-0.0174']",C142081,,,,,,
mondo:0011969,ALG8-congenital disorder of glycosylation,"['carbohydrate deficient glycoprotein syndrome type Ih', 'congenital disorder of glycosylation, type Ih', 'ALG8-CDG', 'ALG8-CDG (CDG-Ih)', 'CDG syndrome type Ih', 'CDG1H', 'CDG 1H', 'congenital disorder of glycosylation type Ih', 'congenital disorder of glycosylation type 1h', 'glucosyltransferase 2 deficiency', 'CDG-Ih', 'CDG Ih']",0080560,608104,79325,C2931002,"['-0.7075', '0.0558', '0.09546', '-0.1184', '0.1542', '-0.372', '-0.1045', '0.1458', '-0.7495', '-0.2788', '-0.3284', '-0.347', '-0.3572', '0.0723', '-0.6514', '-0.2449', '0.1381', '-0.2148', '-0.2722', '-0.3567', '0.55', '-0.01933', '-0.000427', '0.1558', '0.4126', '0.0229', '-0.2446', '0.2183', '0.3323', '-0.05283', '-0.01313', '0.4253', '0.704', '0.1448', '-0.1427', '-0.2961', '0.1532', '0.293', '-0.596', '-0.01472', '-0.788', '0.1476', '0.41', '0.1481', '-0.4192', '0.1771', '-0.01651', '0.1606', '0.107', '0.181', '-0.429', '0.1758', '0.05948', '0.007477', '-0.3127', '-0.1353', '0.2622', '0.00809', '-0.3125', '0.7104', '0.1796', '0.1448', '0.2952', '0.0786', '-0.001907', '-0.1486', '0.2656', '0.3906', '-0.4072', '0.3418', '-0.894', '0.5283', '0.3162', '-0.0963', '0.296', '0.003305', '0.6284', '0.0639', '-0.1624', '-0.01539', '-0.2883', '-0.4365', '0.2632', '0.1677', '0.07666', '0.1743', '0.3464', '0.497', '0.4866', '-0.1803', '-0.3093', '0.6055', '0.3599', '-0.03558', '0.2988', '0.867', '0.5845', '-0.11456', '0.3516', '0.271']",,,C535746,,,,
mondo:0011970,rolandic epilepsy-paroxysmal exercise-induced dystonia-writer^s cramp syndrome,"['epilepsy, ROLANDIC, with paroxysmal exercise-induced dystonia and writer^S cramp', 'Re-ped-Wc', 'epilepsy, rolandic, with paroxysmal exercise-induce dystonia and writer^s cramp', 'EPRPDC']",0111645,608105,163727,C1842531,"['0.9062', '0.2646', '-0.2598', '-0.10126', '-0.2964', '-0.3796', '0.8247', '0.2737', '-0.6187', '-0.4446', '0.1625', '-0.2472', '-0.6016', '0.2375', '0.088', '0.1225', '-0.3306', '-0.632', '-0.5967', '-0.6436', '-0.305', '0.7007', '0.05273', '-0.4917', '-0.3232', '-0.0668', '-0.06586', '-0.1508', '-0.4824', '0.3928', '0.1461', '-0.5483', '0.3943', '0.2295', '0.7915', '0.517', '-0.1048', '-0.01863', '-0.107', '-0.3713', '-0.1924', '-0.179', '0.04163', '-0.3328', '-0.4634', '-0.6743', '-0.35', '0.2134', '0.522', '0.734', '-0.3215', '0.1426', '-0.0633', '-0.542', '0.03387', '-0.2068', '-0.0685', '0.0844', '-0.1395', '0.3333', '-0.8877', '0.5625', '0.568', '-0.2253', '-0.459', '1.62', '-0.01854', '0.1383', '-0.941', '0.7783', '1.061', '0.982', '-0.04883', '-0.2349', '0.1958', '0.6816', '0.9233', '0.5566', '-0.389', '0.2003', '-0.1225', '0.9424', '0.4607', '0.4045', '0.4363', '0.2297', '0.1733', '0.65', '0.8613', '0.3276', '0.02112', '-0.02292', '-0.2214', '0.1243', '0.212', '0.3489', '0.555', '-0.5967', '0.1095', '0.2615']",,,C535499,,,,
mondo:0011971,hyper-IgM syndrome type 5,"['immunodeficiency with hyper IgM, type 5', 'hyper-IgM syndrome due to uracil N-glycosylase', 'hyper IgM syndrome 5', 'hyper-IgM syndrome 5', 'hyper-IgM syndrome caused by mutation in UNG', 'immunodeficiency with hyper IgM type 5', 'UNG hyper-IgM syndrome', 'immunodeficiency with hyper-IgM, type 5', 'hyper-IgM syndrome due to UNG deficiency', 'HIGM5']",0060759,608106,101092,,"['-0.1589', '0.2102', '0.013214', '0.01258', '0.08307', '-0.2888', '-0.04584', '0.05917', '-0.2494', '-0.08325', '-0.04233', '0.03778', '-0.02763', '0.03372', '0.07086', '-0.1809', '-0.04147', '-0.03894', '-0.05356', '-0.2389', '0.0617', '-0.05212', '0.1832', '-0.0824', '0.1309', '0.05194', '-0.09326', '0.0276', '0.02573', '-0.0777', '0.1472', '0.03592', '0.1743', '0.076', '0.1236', '-0.149', '-0.04688', '-0.087', '0.002846', '-0.2261', '0.06354', '-0.1632', '0.11224', '-0.0667', '-0.1621', '-0.2588', '-0.01011', '0.0876', '0.1395', '-0.01904', '0.03784', '-0.10864', '0.01169', '0.01145', '-0.1741', '-0.167', '0.2793', '-0.003685', '-0.2125', '0.0722', '0.0735', '0.11096', '0.11383', '0.03333', '0.11237', '0.0895', '0.162', '-0.00912', '-0.198', '0.1643', '-0.2168', '-0.0329', '0.0704', '-0.1915', '0.1342', '0.01486', '-0.0825', '0.06934', '-0.1627', '-0.0404', '-0.03348', '-0.007687', '-0.03513', '0.101', '-0.0896', '-0.2079', '0.1787', '0.3472', '0.1917', '0.1007', '0.08966', '0.077', '0.0286', '-0.1366', '0.4265', '0.1714', '0.2125', '-0.413', '-0.01454', '-0.03378']",,,,,,,
mondo:0011972,ovarian hyperstimulation syndrome,"['ovarian hyperstimulation syndrome', 'ovarian hyperstimulation syndrome, familial gestational spontaneous', 'secondary Meig^s syndrome', 'OHSS']",5425,608115,64739,C0085083,"['-0.1984', '0.1584', '0.2517', '-0.01446', '-0.053', '-0.617', '-0.0738', '0.3047', '-0.3228', '-0.2233', '-0.1968', '0.5293', '0.6133', '0.574', '-0.716', '-0.1887', '-0.4148', '0.4136', '0.1957', '-0.5034', '-0.1838', '0.2744', '0.06323', '-0.8506', '0.0666', '-0.3696', '0.281', '0.2421', '0.4958', '-0.1383', '0.4597', '-0.2598', '1.0205', '-0.549', '-0.5806', '0.05365', '-0.3638', '0.7', '0.1078', '0.07874', '0.728', '-0.3132', '0.1514', '-0.525', '0.555', '-0.4246', '-0.585', '-0.396', '-0.002235', '0.6216', '-0.04633', '-0.1152', '0.2842', '-0.116', '-0.4072', '0.569', '-0.1388', '0.3184', '-0.7505', '-0.11285', '-0.3298', '0.4524', '-0.1512', '-0.569', '-0.608', '0.1538', '0.3875', '0.592', '-0.4106', '0.5654', '0.3635', '0.2227', '0.2886', '-0.549', '0.07056', '0.377', '0.03333', '0.04382', '0.7095', '-0.02583', '-0.429', '0.3005', '-0.1385', '-0.6245', '0.10406', '0.0882', '-0.00394', '-0.4595', '0.2427', '-0.0398', '0.3176', '0.538', '-0.5605', '0.4114', '-0.1445', '0.1943', '-0.03262', '-0.931', '-0.39', '-0.1311']",,,D016471,256.1,,10033266,
mondo:0011973,"zinc deficiency, transient neonatal","['zinc deficiency, transient neonatal', 'TNZD', 'zinc in breast milk, reduced', 'zinc deficiency, neonatal, due to Low breast milk zinc']",,608118,,C1842486,"['-0.014046', '0.03586', '-0.01208', '-0.002256', '0.02052', '-0.03555', '0.00248', '0.04224', '-0.0332', '-0.008835', '-0.010506', '-0.0002537', '-0.004585', '-0.003056', '-0.02661', '-0.03134', '0.004456', '-0.0238', '-0.0263', '-0.0782', '-0.00927', '-0.01604', '0.03168', '-0.01582', '0.01125', '-0.01378', '-0.003313', '0.01137', '-0.00523', '-0.01657', '0.03467', '0.006577', '0.03943', '0.02269', '-0.00826', '-0.02016', '-0.01024', '-0.002623', '-0.003233', '-0.03363', '0.014114', '-0.0368', '0.03029', '-0.006084', '0.002974', '-0.02538', '-0.01028', '0.01912', '0.002457', '0.02109', '-0.01753', '-0.01045', '0.001701', '0.005764', '-0.00933', '-0.006096', '0.02885', '-0.01396', '-0.03714', '0.02046', '0.02454', '0.01872', '0.009254', '0.00925', '0.01353', '-0.006252', '0.05002', '0.03418', '-0.04047', '0.03836', '-0.02162', '-0.000545', '0.00574', '-0.009476', '0.001854', '0.0114', '0.02362', '-0.01414', '-0.0174', '-0.011314', '0.0007586', '-0.0082', '-0.01993', '0.01941', '0.01593', '0.005707', '0.01243', '0.02866', '0.06195', '0.00962', '0.0207', '0.03995', '-0.007355', '-0.007725', '0.074', '0.0191', '0.03766', '-0.0622', '-0.000871', '0.0148']",,,C564286,,,,
mondo:0011974,retinitis pigmentosa 7,"['retinitis pigmentosa type 7', 'RP7', 'leber congenital amaurosis 18, autosomal recessive, autosomal dominant, digenic dominant', 'retinitis pigmentosa 7, digenic form, autosomal recessive, autosomal dominant, digenic dominant', 'RP 7', 'retinitis pigmentosa 7 and digenic form, autosomal recessive, autosomal dominant, digenic dominant', 'Leber congenital amaurosis 18', 'retinitis pigmentosa 7', 'retinitis pigmentosa 7, digenic']",0110383,608133,,C1842475,,,,,,H35.5,,
mondo:0011975,paternal uniparental disomy of chromosome 14,"['UPD(14)pat', 'paternal uniparental disomy 14', 'KAGAMI-Ogata syndrome', 'paternal uniparental disomy of chromosome type 14', 'uniparental disomy, paternal, chromosome 14']",,608149,96334,C1842466,,,,C536471,,,,
mondo:0011976,lipodystrophy-intellectual disability-deafness syndrome,"['lipodystrophy, generalized, with intellectual disability, deafness, short stature, and slender bones', 'lipodystrophy, generalized, with mental retardation, deafness, short stature, and slender bones', 'Rajab-Spranger syndrome']",,608154,50811,,,,,C564283,,,,
mondo:0011977,8q22.1 microdeletion syndrome,"['NMLFS', 'Nablus mask-like facial syndrome', 'chromosome 8Q22.1 deletion syndrome', 'NABLUS mask-like facial syndrome', 'monosomy 8q22.1']",,608156,178303,C1842464,,,,C536110,,,,
mondo:0011978,CoQ-responsive OXPHOS deficiency,['CoQ-responsive OXPHOS deficiency'],,608158,,C1842463,,,,C535470,,,,
mondo:0011979,adult-onset foveomacular vitelliform dystrophy,"['adult-onset vitelliform macular dystrophy', 'pseudo-Best disease', 'macular dystrophy, vitelliform, 3', 'adult-onset foveomacular dystrophy with choroidal neovascularization', 'adult-onset foveomacular dystrophy', 'macular dystrophy, vitelliform, adult-onset', 'pseudo-vitelliform macular dystrophy', 'AOFMD', 'VMD3', 'Gass disease', 'AVMD', 'macular dystrophy, vitelliform, type 3', 'foveomacular dystrophy, adult-onset, with choroidal neovascularization', 'foveomacular dystrophy, adult-onset; AOFMD']",,,99000,C1842914,"['-0.7256', '-0.3555', '-0.05145', '0.2128', '0.242', '-0.2908', '-0.2976', '0.524', '-0.2477', '0.04623', '0.0875', '-0.2119', '-0.38', '0.4995', '0.2284', '-0.2517', '0.2742', '-0.411', '0.2365', '-0.9473', '-0.6265', '0.03397', '0.0825', '0.0983', '-0.118', '-0.1342', '-0.01631', '-0.007618', '-0.279', '0.3552', '0.7573', '-0.2378', '0.02858', '-0.1627', '-0.1494', '0.309', '0.365', '-0.4517', '0.1312', '-0.7715', '0.615', '-0.231', '0.404', '-0.2413', '-0.4683', '0.06125', '-0.611', '-0.698', '-0.2644', '0.08014', '0.561', '0.2238', '0.1788', '-0.656', '0.3252', '0.2583', '0.919', '-0.2617', '-0.8413', '0.049', '-0.1237', '-0.0446', '0.1161', '0.5703', '-0.01247', '0.03897', '0.6445', '0.557', '-0.0748', '0.6143', '-0.1481', '-0.448', '0.261', '-0.181', '0.2822', '-0.0931', '0.254', '-0.10803', '0.02158', '-0.00656', '0.754', '0.04272', '0.1009', '0.561', '0.1201', '-0.05655', '-0.0699', '-0.2668', '0.403', '0.4766', '0.00887', '0.3757', '-0.2454', '0.65', '0.6943', '-0.4893', '0.0688', '-0.3057', '-0.2666', '-0.05148']",,,,,H35.5,,
mondo:0011980,"autoimmune thyroid disease, susceptibility to, 1","['AITD1', 'autoimmune thyroid disease, susceptibility to, 1', 'autoimmune thyroid disease, susceptibility to, type 1']",,608173,,C1842446,,,,,,,,
mondo:0011981,"autoimmune thyroid disease, susceptibility to, 2","['autoimmune thyroid disease, susceptibility to, 2', 'AITD2', 'autoimmune thyroid disease, susceptibility to, type 2']",,608174,,C1842445,,,,,,,,
mondo:0011982,"autoimmune thyroid disease, susceptibility to, 3","['autoimmune thyroid disease, susceptibility to, 3', 'autoimmune thyroid disease, susceptibility to, type 3', 'AITD3']",,608175,,,,,,,,,,
mondo:0011983,"autoimmune thyroid disease, susceptibility to, 4","['autoimmune thyroid disease, susceptibility to, 4', 'autoimmune thyroid disease, susceptibility to, type 4', 'AITD4']",,608176,,C1842443,,,,,,,,
mondo:0011984,synpolydactyly type 2,"['synpolydactyly, 3/3^4, associated with metacarpal and metatarsal synostoses', 'SPD, Debeer type', 'synpolydactyly type 2', 'synpolydactyly 2', 'SD2b', 'SD2, Debeer type', 'SPD2', 'FBLN1 non-syndromic synpolydactyly', 'synpolydactyly, 3/3-prime/4, associated with metacarpal and metatarsal synostoses', 'synpolydactyly, Debeer type', 'non-syndromic synpolydactyly caused by mutation in FBLN1']",,608180,295197,C1842422,"['-0.136', '-0.00881', '0.3123', '0.1726', '0.2286', '-0.401', '-0.2046', '0.089', '-0.4133', '-0.3088', '-0.0386', '0.003395', '-0.0669', '0.1736', '0.006706', '-0.2025', '0.1775', '-0.10974', '0.0793', '-0.296', '0.0994', '0.19', '0.423', '-0.10187', '0.34', '0.10095', '0.04782', '0.1716', '-0.05072', '-0.03848', '0.00647', '-0.488', '0.0987', '0.0628', '0.3464', '-0.1364', '0.0393', '0.02122', '0.08905', '-0.6787', '0.1532', '-0.3445', '0.2413', '0.01262', '0.2595', '-0.5767', '0.0517', '0.3809', '-0.08997', '0.01089', '0.2463', '-0.0875', '0.2491', '0.1661', '-0.2605', '-0.5093', '0.2339', '0.1879', '-0.238', '0.08563', '0.237', '0.145', '0.03885', '0.3262', '0.0182', '0.282', '0.212', '0.04', '-0.1339', '0.1062', '-0.3303', '0.0231', '0.3032', '-0.3562', '0.07355', '0.2184', '-0.1575', '0.1929', '-0.3757', '-0.522', '-0.332', '-0.05362', '0.1992', '0.1027', '0.03452', '-0.3145', '-0.3193', '0.1528', '-0.08984', '-0.268', '-0.2769', '0.1104', '0.1179', '-0.10065', '0.486', '0.12445', '0.3066', '-0.723', '0.3667', '0.04028']",,,C564278,,,,
mondo:0011985,hyper-IgM syndrome type 4,"['hyper-IgM syndrome 4', 'immunodeficiency with hyper-IgM type 4', 'immunodeficiency with hyper IgM type 4', 'hyper IgM syndrome 4', 'HIGM4', 'immunodeficiency with hyper-IgM, type 4', 'hyper-IgM syndrome type 4']",0060760,608184,101091,C1842413,,,,C564277,,,,
mondo:0011986,tropical pancreatitis,"['tropical calcific chronic pancreatitis', 'TCP', 'tropical calcific pancreatitis', 'fibrocalculous pancreatic diabetes, susceptibility to']",,608189,103918,C4510860,,,,C564276,,,,
mondo:0011987,cone-rod dystrophy 13,"['cone-rod dystrophy 13', 'cone-rod dystrophy caused by mutation in RPGRIP1', 'CORD13', 'cone-rod dystrophy type 13', 'RPGRIP1 cone-rod dystrophy']",0111016,608194,,C2750720,,,,C567698,,,,
mondo:0011988,neutrophil immunodeficiency syndrome,"['neutrophil immunodeficiency syndrome', 'immunodeficiency 73A with defective neutrophil chemotaxix and leukocytosis']",0112064,608203,183707,C1842398,"['-0.2443', '-0.2352', '0.0735', '-0.2126', '-0.005234', '-0.4731', '0.038', '-0.02786', '0.2773', '-0.1049', '0.0442', '-0.2489', '-0.3406', '-0.3704', '0.19', '-0.0569', '0.1556', '0.0466', '-0.4739', '-0.731', '-0.2037', '-0.2339', '0.806', '-0.3276', '0.116', '0.03494', '-0.153', '0.01617', '-0.02615', '-0.0464', '0.2404', '0.3064', '0.04156', '-0.259', '0.0917', '0.0341', '-0.2534', '-0.4468', '-0.1561', '-0.1775', '-0.05338', '-0.2125', '-0.2925', '-0.3074', '-0.014366', '-0.1465', '-0.06805', '-0.0576', '0.0917', '0.1428', '-0.1044', '-0.2598', '0.1265', '0.2866', '-0.5166', '0.09503', '0.285', '-0.2347', '-0.4238', '0.292', '-0.081', '0.3127', '0.10016', '-0.11005', '0.6045', '0.11395', '0.0747', '0.0125', '-0.4873', '0.5654', '-0.6494', '-0.4373', '-0.006603', '-0.2905', '0.2146', '-0.02524', '0.2996', '0.2225', '0.324', '0.3967', '-0.0693', '-0.1395', '-0.1437', '0.1475', '0.1111', '-0.1324', '0.6675', '0.3735', '0.42', '-0.1804', '0.2311', '0.4417', '-0.003874', '0.2664', '0.661', '0.854', '0.2593', '-0.569', '0.2717', '-0.2433']",,,C564275,,,,
mondo:0011989,leishmaniasis,"['cutaneous leishmaniasis (subtype)', 'post-kala-azar dermal infectious disease by leishmaniasis', 'visceral leishmaniasis (subtype)', 'post kala-Azar dermal leishmaniasis', 'post-kala-azar dermal leishmaniasis']",9065,,507,C0023281,,C34767,0005044,D007896,085.9,B55,10024198,
mondo:0011990,"seizures, benign familial neonatal, 3","['BFNS3', 'seizures, benign familial neonatal, 3', 'convulsions, benign familial neonatal, 3']",,608217,,C1842382,,,,C564274,,,,
mondo:0011991,autosomal recessive nonsyndromic hearing loss 38,"['autosomal recessive nonsyndromic deafness type 38', 'DFNB38', 'autosomal recessive nonsyndromic deafness 38', 'autosomal recessive deafness 38', 'deafness, autosomal recessive 38']",0110496,608219,,C1842381,,,,C564273,,,,
mondo:0011992,hereditary spastic paraplegia 25,"['spastic paraplegia 25, autosomal recessive', 'spinal disc herniation with autosomal recessive spastic paraplegia', 'Disc herniation with spastic paraplegia, autosomal recessive', 'hereditary spastic paraplegia type 25', 'SPG25', 'autosomal recessive spastic paraplegia-disc herniation syndrome', 'spinal disk herniation with autosomal recessive spastic paraplegia', 'autosomal recessive spastic paraplegia 25', 'spastic paraplegia 25', 'autosomal recessive spastic paraplegia type 25']",0110776,608220,101005,C4518003,,,,C536861,,,,
mondo:0011993,aspirin resistance,"['aspirin, resistance to Antithrombotic Effect of', 'aspirin resistance', 'aspirin, resistance to Cardioprotective Effect of']",,608223,,,,,,,,,,
mondo:0011994,autosomal dominant nonsyndromic hearing loss 41,"['autosomal dominant nonsyndromic deafness caused by mutation in P2RX2', 'P2RX2 autosomal dominant nonsyndromic deafness', 'autosomal dominant deafness 41', 'DFNA41', 'deafness, autosomal dominant type 41', 'deafness, autosomal dominant 41', 'autosomal dominant nonsyndromic deafness 41', 'autosomal dominant nonsyndromic deafness type 41']",0110567,608224,,C1842371,,,,C564272,,,,
mondo:0011995,cataract - congenital heart disease - neural tube defect syndrome,"['craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developintellectual disability', 'craniofacial abnormalities, cataracts, congenital heart disease, sacral neural tube defects, and growth and developmental retardation']",,608227,314993,C1842363,,,,C564271,,,,
mondo:0011996,"chronic myelogenous leukemia, BCR-ABL1 positive","['CML - chronic myelogenous leukaemia', 'chronic myelocytic leukemia', 'chronic myelogenous leukemia', 'BCR-ABL Positive chronic myelogenous leukaemia', 'leukemia, chronic myeloid', 'CML', 'chronic granulocytic leukaemia', 'hematopoeitic - chronic myelocytic leukemia (CML)', 'chronic myelogenous leukaemia (CML)', 'chronic myelogenous leukemia, BCR-ABL1 Positive', 'leukemia, chronic myelogenous', 'leukemia, chronic myeloid, Philadelphia chromosome positive, somatic', 'hematopoeitic - chronic myelocytic leukaemia (CML)', 'leukemia, chronic myeloid, atypical', 'chronic myelogenous leukemias', 'myeloid leukemia, chronic', 'BCR-ABL Positive chronic myelogenous leukemia', 'chronic myelogenous leukemia (CML)', 'chronic myelocytic leukaemia', 'chronic granulocytic leukemia', 'chronic myelogenous leukaemia', 'leukemia, Philadelphia chromosome-positive, resistant to imatinib, Somatic mutation', 'chronic myeloid leukemia', 'chronic myeloid leukaemia', 'CML - chronic myelogenous leukemia']",8552,608232,521,C0023473,"['0.3535', '-0.1548', '-0.188', '0.1334', '-0.3398', '-0.3867', '0.7573', '1.439', '0.06088', '-0.3152', '0.05502', '0.3687', '0.2003', '0.4023', '-0.2', '0.2358', '-0.134', '-0.6006', '-0.1696', '-0.2496', '-0.2969', '-0.119', '0.6494', '-0.969', '0.3882', '-0.2551', '-0.00703', '-0.654', '-0.639', '0.0737', '0.8955', '0.7725', '0.6123', '0.11487', '0.3196', '0.4006', '-1.089', '0.2856', '0.3281', '-0.2803', '0.0534', '0.2952', '-0.0879', '-0.296', '-0.2094', '-0.2081', '-0.202', '-0.595', '0.255', '-0.4773', '0.503', '-0.1304', '0.3591', '-0.338', '0.9663', '-0.05768', '-0.448', '-0.2231', '-0.6426', '-0.3293', '0.2664', '0.35', '0.1901', '-0.668', '-0.2296', '0.05966', '0.2544', '-0.1906', '0.282', '1.402', '-0.205', '-0.163', '-0.294', '-0.1866', '0.6724', '0.2352', '0.008606', '0.4773', '-0.00779', '-0.3079', '-0.639', '-0.413', '0.05728', '-0.02426', '-0.652', '-0.4246', '0.4844', '0.502', '0.2402', '0.104', '0.01802', '-0.1434', '-0.528', '-0.1636', '0.8057', '0.9976', '-0.4153', '-0.7056', '-0.169', '-0.2656']",C3177,0000339,,205.1,,10009013,
mondo:0011997,Hermansky-Pudlak syndrome 2,"['Hermansky Pudlak syndrome 2', 'Hermansky-Pudlak syndrome type 2', 'HPS-2', 'Platelet defects and oculocutaneous albinism', 'Hermansky-Pudlak syndrome 2', 'Hermansky-Pudlak syndrome caused by mutation in AP3B1', 'AP3B1 Hermansky-Pudlak syndrome', 'Hermansky-Pudlak syndrome with neutropenia', 'HPS2']",0060540,608233,183678,C1842362,"['0.05106', '-0.278', '-0.3618', '-0.5737', '0.0917', '0.1316', '-0.4702', '0.6123', '0.06445', '-0.01569', '-0.1094', '-0.394', '-0.2815', '-0.2173', '-0.1747', '0.10535', '0.5527', '0.0674', '0.287', '-0.6436', '-0.2004', '-0.5854', '0.566', '-0.834', '-0.521', '-0.2278', '-0.4531', '0.10913', '0.482', '-0.1603', '0.479', '0.1024', '0.3792', '0.3284', '0.0654', '-0.196', '-0.4087', '-0.3545', '-0.2993', '-0.149', '1.129', '-0.09155', '-0.3398', '-0.1487', '-0.007687', '0.05807', '0.2542', '-0.1761', '0.4065', '-0.1508', '0.3481', '-0.3052', '0.1932', '0.4658', '0.4768', '0.1654', '0.2798', '-0.4258', '-0.09863', '-0.6235', '-0.187', '-0.5967', '-0.04272', '-0.1714', '0.2744', '0.1726', '0.4001', '0.08386', '-0.5225', '0.5776', '-0.4453', '-1.097', '-0.2213', '-0.522', '0.5913', '0.1407', '0.526', '-0.1285', '0.3206', '0.567', '0.322', '-0.3835', '0.4172', '0.637', '-0.346', '-0.02663', '0.3997', '0.694', '0.801', '-0.1964', '0.653', '0.9985', '0.3838', '0.0979', '1.105', '0.1493', '-0.3064', '-0.052', '-0.06775', '0.4375']",C150368,,C537709,,E70.3,,
mondo:0011998,autosomal dominant slowed nerve conduction velocity,"['slowed nerve conduction velocity, AD', 'slowed nerve conduction velocity, autosomal dominant', 'SNCV']",,608236,140481,C1842357,"['-0.759', '-0.0875', '0.698', '-0.1076', '0.0716', '-0.2842', '-0.449', '0.6914', '-0.445', '-0.099', '-0.0731', '-0.2238', '-0.4478', '-0.4219', '0.729', '0.10443', '0.2059', '-0.2942', '-0.238', '-0.7007', '0.3228', '-0.11365', '0.173', '0.5835', '0.3145', '0.1409', '0.069', '0.08044', '0.02592', '-0.3447', '0.5254', '-0.0927', '0.6636', '0.2395', '-0.2578', '-0.21', '-0.08875', '0.02046', '0.2014', '-0.57', '-0.142', '-0.3', '-0.04843', '0.5083', '-0.0355', '-0.4614', '-0.3528', '0.4226', '0.1725', '0.1236', '0.116', '0.1873', '-0.678', '-0.2212', '0.1159', '-0.2705', '0.6504', '-0.1327', '-0.66', '0.3599', '0.01741', '-0.0538', '0.623', '0.3157', '-0.2041', '0.2542', '0.04242', '0.6987', '-0.1764', '0.1812', '-0.3284', '0.302', '0.3535', '-0.05603', '0.772', '-0.3633', '0.0918', '0.3918', '-0.03038', '-0.3577', '-0.1577', '-0.593', '0.03702', '0.4746', '-0.2325', '-0.2152', '0.1987', '0.5713', '0.4429', '0.1604', '-0.06433', '0.0919', '0.0968', '0.1262', '0.4954', '0.4692', '0.45', '0.1316', '0.0912', '0.2043']",,,C564269,,,,
mondo:0011999,otosclerosis 3,"['OTSC3', 'otosclerosis 3']",,608244,,C1842353,,,,C564268,,,,
mondo:0012000,specific phobia,"['simple phobia', 'phobia, simple', 'phobia, specific']",599,608251,,,,C35284,1001918,C562465,300.29,,,
mondo:0012001,"mandibulofacial dysostosis with ptosis, autosomal dominant","['mandibulofacial dysostosis with ptosis, autosomal dominant']",,608257,,C1842349,,,,C564267,,,,
mondo:0012002,autosomal recessive nonsyndromic hearing loss 40,"['autosomal recessive nonsyndromic deafness 40', 'autosomal recessive nonsyndromic deafness type 40', 'deafness, autosomal recessive 40', 'autosomal recessive deafness 40', 'DFNB40']",0110499,608264,,C1842345,,,,C564266,,,,
mondo:0012003,autosomal recessive nonsyndromic hearing loss 39,"['autosomal recessive nonsyndromic deafness type 39', 'deafness, autosomal recessive 39', 'autosomal recessive nonsyndromic deafness caused by mutation in HGF', 'HGF autosomal recessive nonsyndromic deafness', 'autosomal recessive deafness 39', 'autosomal recessive nonsyndromic deafness 39', 'deafness, autosomal recessive type 39', 'DFNB39']",0110497,608265,,C1842342,,C129874,,C564265,,,,
mondo:0012004,parathyroid gland carcinoma,"['malignant tumour of parathyroid gland', 'carcinoma of the parathyroid', 'carcinoma of parathyroid', 'carcinoma of parathyroid gland', 'carcinoma of the parathyroid gland', 'parathyroid adenocarcinoma', 'parathyroid gland carcinoma', 'parathyroid cancer', 'parathyroid gland neoplasm', 'adenocarcinoma of the parathyroid', 'adenocarcinoma of parathyroid', 'adenocarcinoma of parathyroid gland', 'malignant neoplasm of the parathyroid', 'parathyroid neoplasm', 'cancer of the parathyroid gland', 'parathyroid gland adenocarcinoma', 'cancer of parathyroid gland', 'parathyroid carcinoma', 'malignant neoplasm of parathyroid gland', 'parathyroid gland cancer', 'adenocarcinoma of the parathyroid gland', 'PRTC']",1540,608266,143,,"['-0.2896', '0.1378', '-0.04996', '-0.1521', '-0.2576', '0.2607', '0.1449', '0.2003', '-0.1202', '-0.068', '-0.2917', '0.003002', '-0.4163', '0.443', '-0.0672', '-0.03854', '-0.08093', '-0.2766', '0.1324', '-0.7173', '0.1372', '-0.282', '0.6147', '-0.1109', '0.1343', '0.0467', '0.04932', '-0.3394', '-0.3442', '0.004757', '0.3752', '-0.1438', '0.306', '-0.262', '-0.01467', '-0.1902', '-0.3147', '0.0536', '-0.00508', '0.1918', '-0.06445', '-0.052', '0.4153', '-0.3809', '0.5146', '-0.01508', '-0.1581', '-0.4346', '0.2886', '0.396', '0.2847', '0.2886', '0.07025', '0.3105', '-0.672', '-0.01467', '0.05847', '-0.1389', '-0.319', '0.1691', '0.5674', '0.03888', '-0.4363', '-0.1344', '-0.3525', '0.545', '0.2339', '0.5635', '-0.1389', '0.2007', '0.06604', '-0.1533', '0.4111', '0.0807', '0.04626', '-0.1962', '0.2329', '0.521', '0.201', '-0.6187', '-0.527', '0.1207', '0.2389', '-0.0835', '-0.4136', '-0.3784', '0.2825', '0.01776', '0.441', '-0.04855', '0.02892', '0.2308', '0.02562', '-0.3098', '0.794', '-0.02155', '0.3477', '-0.1613', '-0.006676', '0.2186']",C4906,1000456,,194.1,,,
mondo:0012005,"growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy","['growth failure, microcephaly, intellectual disability, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy', 'growth failure, microcephaly, mental retardation, cataracts, large joint contractures, osteoporosis, cortical dysplasia, and cerebellar atrophy']",,608278,,C1842321,,,,C564264,,,,
mondo:0012006,craniosynostosis with ocular abnormalities and hallucal defects,['craniosynostosis with ocular abnormalities and hallucal defects'],,608279,,C1842316,,,,C564263,,,,
mondo:0012007,"scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities","['scimitar anomaly, multiple cardiac malformations, and craniofacial and central nervous system abnormalities', 'anomalous pulmonary Venous return, multiple Cardiac malformations, and craniofacial and central nervous system abnormalities']",,608281,,C1842315,,,,C564262,,,,
mondo:0012008,Lelis syndrome,"['ectodermal dysplasia, hypohidrotic, with acanthosis nigricans', 'Lelis syndrome', 'ectodermal dysplasia-acanthosis nigricans syndrome']",,608290,140936,C1842307,,,,C564261,,,,
mondo:0012009,"coronary heart disease, susceptibility to, 2","['coronary heart disease, susceptibility to, 2', 'Chds2', 'coronary heart disease, susceptibility to, type 2']",,608316,,C1842260,,,,,,,,
mondo:0012010,"coronary heart disease, susceptibility to, 4","['coronary heart disease, susceptibility to, 4', 'coronary heart disease, susceptibility to, type 4', 'Chds4']",,608318,,C1842258,,,,,,,,
mondo:0012011,"coronary artery disease, autosomal dominant, 1","['coronary artery disease, autosomal dominant, 1', 'coronary artery disease, autosomal dominant, type 1', 'ADCAD1', 'coronary artery disease with myocardial infarction', 'MEF2A coronary artery disease', 'coronary artery disease caused by mutation in MEF2A']",,608320,,C1842247,,,,C564258,,,,
mondo:0012012,Charcot-Marie-Tooth disease dominant intermediate C,"['autosomal dominant intermediate Charcot-Marie-Tooth disease type C', 'Charcot-Marie-Tooth neuropathy dominant intermediate C', 'Charcot-Marie-Tooth neuropathy, dominant Intermediate C', 'Charcot-Marie-Tooth disease, dominant Intermediate type C', 'Di-Cmtc', 'Charcot-Marie-Tooth disease dominant intermediate type C', 'CMTDIC', 'DI-CMTC', 'YARS Charcot-Marie-Tooth disease', 'YARS-related intermediate Charcot-Marie-Tooth neuropathy', 'Charcot-Marie-Tooth disease caused by mutation in YARS', 'Charcot-Marie-Tooth disease, dominant intermediate C']",0110199,608323,100045,C1842237,"['-0.0684', '0.1888', '0.1439', '0.2498', '-0.227', '-0.004047', '-0.2053', '0.6045', '-0.889', '0.02673', '-0.2246', '0.07654', '-0.664', '-0.02232', '-0.11096', '0.1092', '-0.253', '-0.3162', '-0.335', '-0.6772', '0.0447', '0.5396', '0.09283', '0.9556', '0.44', '0.5024', '-0.06506', '0.0675', '-0.0302', '-0.3506', '0.3528', '-0.737', '0.329', '0.0909', '0.4377', '-0.928', '-0.6436', '-0.2844', '0.807', '-0.1654', '-1.417', '-0.2898', '-0.6074', '0.4705', '-0.3079', '-0.0806', '-0.2617', '0.1346', '-0.227', '-0.3804', '0.3174', '0.2798', '-0.4084', '-0.863', '0.1072', '-0.3928', '-0.2386', '0.1979', '-0.9395', '-0.2742', '-0.623', '0.1356', '0.4836', '0.4805', '-0.912', '0.758', '0.1895', '0.7563', '-0.5513', '0.738', '-0.543', '0.1247', '0.2983', '-0.2546', '1.487', '0.777', '-0.03873', '0.3198', '-0.3271', '-0.3662', '-0.3608', '-0.5757', '0.979', '0.4033', '-0.07806', '0.242', '0.211', '1.214', '0.547', '0.11554', '0.4204', '-0.1567', '-0.5234', '0.1382', '0.4353', '0.4226', '0.514', '-0.655', '0.00894', '0.4468']",,,C564257,,,,
mondo:0012013,"Weill-Marchesani syndrome 2, dominant","['WMS2', 'glaucoma-lens ectopia-microspherophakia-stiffness-shortness syndrome', 'GEMSS syndrome', 'glaucoma, ectopia, microspherophakia, Stiff joints and short stature syndrome', 'GEMSS', 'Weill-Marchesani syndrome type 2', 'mesodermal Dysmorphodystrophy, congenital', 'spherophakia-brachymorphia syndrome', 'Weill-Marchesani syndrome, autosomal dominant', 'Weill-Marchesani syndrome 2']",,608328,2084,,"['0.3389', '-0.00525', '-0.633', '0.7524', '0.007717', '-0.1165', '-0.01455', '0.9277', '-0.0946', '-1.051', '0.5127', '-0.05225', '-0.02063', '0.505', '-0.4973', '-0.3481', '-0.03108', '0.127', '0.01651', '-0.574', '0.3074', '0.7627', '-0.1628', '-0.4077', '0.02731', '0.1974', '-0.1465', '0.5107', '0.0787', '0.1604', '0.3972', '-0.4146', '0.571', '0.04828', '-0.524', '0.002087', '0.003256', '-0.899', '0.4734', '-0.4155', '0.5845', '-0.558', '0.609', '-0.4692', '-0.186', '0.832', '0.367', '-0.1014', '0.8296', '-0.3918', '0.1362', '0.0677', '-0.439', '-1.327', '0.8184', '-0.51', '0.262', '0.4802', '-1.153', '-0.579', '-0.1614', '-0.291', '-0.1384', '0.5854', '-0.454', '-0.3604', '0.2961', '0.475', '-0.7153', '0.7793', '0.2166', '0.6265', '0.3696', '-1.142', '-0.1632', '0.15', '0.0708', '0.8076', '0.02515', '0.4038', '0.2617', '-0.04553', '-0.672', '0.9185', '0.214', '0.4211', '0.633', '0.01659', '0.33', '0.811', '-0.4768', '0.1009', '-0.507', '0.0649', '0.9966', '-0.3591', '-0.3213', '-0.1766', '-0.01446', '-0.5156']",,,,,,,
mondo:0012014,Charcot-Marie-Tooth disease recessive intermediate A,"['Ri-Cmta', 'Charcot-Marie-Tooth neuropathy recessive intermediate A', 'Charcot-Marie-Tooth disease, recessive Intermediate type a', 'CMTRIA', 'GDAP1 Charcot-Marie-Tooth disease', 'Charcot-Marie-Tooth disease, recessive intermediate A', 'Charcot-Marie-Tooth disease recessive intermediate type A', 'Charcot-Marie-Tooth disease caused by mutation in GDAP1', 'Charcot-Marie-Tooth disease, recessive intermediate, A', 'RI-CMT type A', 'RI-CMTA', 'autosomal recessive intermediate Charcot-Marie-Tooth disease type A', 'Charcot-Marie-Tooth neuropathy, recessive Intermediate a']",0110201,608340,217055,C1842197,"['0.2491', '0.346', '0.283', '0.1071', '0.01564', '-0.1891', '0.1886', '0.539', '-0.6323', '-0.305', '-0.2023', '0.383', '-0.5728', '0.4404', '-0.11847', '0.1982', '0.00842', '-0.3337', '-0.1572', '-0.5933', '-0.00992', '0.4373', '0.2236', '0.795', '0.2126', '0.3823', '0.13', '0.0985', '0.106', '-0.4595', '0.3728', '-0.5244', '0.301', '0.0702', '0.1146', '-0.685', '-0.4797', '-0.4907', '0.619', '-0.4087', '-1.482', '-0.6006', '-0.4026', '0.354', '-0.1869', '-0.3938', '0.3003', '-0.18', '-0.416', '0.11456', '0.3806', '0.3306', '-0.506', '-1.142', '0.1254', '-0.1405', '-0.4167', '0.4697', '-0.7134', '-0.001916', '-0.1406', '-0.3145', '0.5454', '0.6987', '-0.8657', '1.22', '-0.05643', '0.6875', '-0.497', '0.3486', '-0.85', '0.4287', '0.442', '-0.04276', '1.233', '0.5024', '-0.3748', '0.4705', '0.1104', '-0.576', '-0.0699', '-0.664', '0.607', '0.941', '0.2964', '0.1128', '0.1396', '0.622', '0.4368', '0.689', '0.267', '0.00911', '-0.05173', '0.3394', '0.4744', '0.573', '0.5386', '-0.7744', '0.0956', '0.7466']",,,C564256,,,,
mondo:0012015,"nystagmus 3, congenital, autosomal dominant","['NYSTAGMUS 3, congenital, autosomal dominant', 'NYS3']",0111793,608345,,C1842186,,,,C537855,,,,
mondo:0012016,capillary malformation-arteriovenous malformation syndrome,"['CM-AVM', 'CM-AVM syndrome', 'capillary malformation without arteriovenous malformation', 'CMAVM', 'capillary malformation-arteriovenous malformation']",,,137667,,"['-0.2312', '-0.3945', '-0.0545', '0.02477', '-0.202', '-0.458', '-0.1744', '0.1453', '-0.359', '0.327', '-0.4712', '-0.562', '0.11194', '0.3198', '-0.2761', '-0.3213', '-0.2024', '-0.3699', '-0.1006', '-0.6284', '-0.03732', '0.2256', '-0.3474', '0.199', '0.4937', '-0.4104', '0.002851', '0.1366', '0.4155', '0.0053', '0.323', '-0.4023', '0.6587', '-0.2913', '0.0897', '0.03305', '0.01732', '0.2893', '0.522', '0.124', '1.094', '-0.402', '-0.014694', '-0.4622', '0.812', '0.3137', '-0.0797', '0.0711', '-0.1836', '-0.4602', '-0.0567', '0.437', '0.2096', '-0.1876', '0.06476', '-0.0664', '-0.411', '0.3044', '-0.4941', '0.2137', '-0.3772', '-0.2197', '0.02849', '-0.07294', '-0.1786', '0.536', '0.2585', '0.3025', '0.11237', '1.008', '0.1964', '0.5693', '-0.4375', '-0.4048', '0.3533', '0.2996', '0.315', '0.8203', '-0.2068', '-0.2512', '-0.0809', '0.01845', '-0.2876', '0.2573', '0.0794', '-0.3896', '0.3423', '0.06866', '-0.0673', '-0.264', '-0.1533', '0.3267', '0.5874', '0.5596', '0.3704', '0.386', '0.4077', '-0.35', '0.4578', '0.6626']",C179668,,C564254,747.69,,,
mondo:0012019,"spondyloepiphyseal dysplasia, Kimberley type","['SEDK', 'Sedk', 'spondyloepiphyseal dysplasia, Kimberley type']",0112282,608361,93283,,"['-0.494', '0.4612', '-0.1843', '-0.1169', '0.281', '-0.561', '-0.6826', '0.731', '-0.4946', '-0.4243', '0.54', '-0.0573', '-0.03406', '0.0778', '0.3647', '-0.1292', '0.547', '0.5273', '-0.2367', '-0.257', '-0.0404', '-0.1655', '0.643', '-0.10156', '0.2566', '0.5454', '-0.05173', '-0.2542', '0.05405', '-0.535', '0.4045', '-0.648', '-0.1023', '0.2256', '0.4902', '-0.249', '-0.605', '-0.5327', '0.0111', '-0.6807', '0.1819', '-0.26', '-0.1054', '0.1398', '0.1848', '-0.5693', '0.3247', '0.2598', '0.05045', '-0.614', '0.4263', '0.1658', '-0.1417', '0.11786', '-0.2288', '-1.427', '0.002554', '-0.4', '-0.08606', '-0.332', '0.5767', '0.0819', '-0.4946', '0.3179', '-0.1021', '-0.12244', '0.2482', '0.6265', '-0.5664', '0.334', '-0.369', '-0.0161', '0.0657', '-0.1311', '-0.2522', '0.38', '-0.5713', '0.4358', '-0.3643', '-0.2773', '0.2012', '0.1255', '-0.6045', '0.432', '-0.08563', '0.02446', '0.10925', '0.4402', '0.2051', '0.1525', '-0.3535', '0.014854', '0.1876', '0.0485', '0.601', '0.1451', '0.4958', '0.08105', '-0.0864', '-0.4368']",,,C564252,,,,
mondo:0012020,chromosome 22q11.2 microduplication syndrome,"['dup(22)(q11)', '22q11 duplication syndrome', 'duplication 22q11.2', 'chromosome 22q11.2 duplication syndrome', 'chromosome 22q11.2 DUPLICATION syndrome', 'Duplication 22q11.2', 'chromosome 22q11.2 microduplication syndrome, isolated cases', '22q11.2 duplication', '22q11.2 microduplication syndrome', '22q11.2 duplication syndrome', 'trisomy 22q11.2', 'chromosome 22q11.2 microduplication syndrome']",0060436,608363,1727,C2675369,,,,C567224,758.5,,,
mondo:0012021,"myopia 17, autosomal dominant","['MYP17', 'myopia 4, formerly', 'myopia 17, autosomal dominant', 'myopia 4']",,608367,,C3888211,,,,,,,,
mondo:0012022,orofacial cleft 4,"['cleft lip with or without cleft palate, nonsyndromic, 4', 'OFC4', 'orofacial cleft 4']",0080398,608371,,C1842143,,,,C564251,,,,
mondo:0012023,autosomal dominant nonsyndromic hearing loss 49,"['autosomal dominant nonsyndromic deafness 49', 'autosomal dominant deafness 49', 'autosomal dominant nonsyndromic deafness type 49', 'DFNA49', 'deafness, autosomal dominant 49']",0110572,608372,,C1842136,,,,C564250,,,,
mondo:0012024,retinitis pigmentosa 26,"['retinitis pigmentosa 26', 'RP26', 'RP 26', 'retinitis pigmentosa caused by mutation in CERKL', 'retinitis pigmentosa type 26', 'CERKL retinitis pigmentosa']",0110368,608380,,C1842127,,,,C564249,,H35.5,,
mondo:0012025,branchiootic syndrome 3,"['branchiootic syndrome type 3', 'BOS3', 'branchiootic syndrome 3', 'branchiootic syndrome caused by mutation in SIX1', 'bo syndrome 3', 'SIX1 branchiootic syndrome']",,608389,,C1842124,,,,C564248,,,,
mondo:0012027,"autoimmune disease, susceptibility to, 2","['autoimmune disease susceptibility locus, chromosome 7-related', 'autoimmune disease, susceptibility to, 2', 'vitiligo-associated multiple autoimmune disease susceptibility 3', 'AIS2']",,608391,,,,,,,,,,
mondo:0012028,"autoimmune disease, susceptibility to, 3","['autoimmune disease, susceptibility to, 3', 'AIS3', 'autoimmune disease susceptibility locus, chromosome 8-related', 'vitiligo-associated multiple autoimmune disease susceptibility 4']",,608392,,,,,,,,,,
mondo:0012029,"microcephaly 6, primary, autosomal recessive","['CENPJ autosomal recessive primary microcephaly', 'MCPH6', 'microcephaly 6, primary, autosomal recessive', 'autosomal recessive primary microcephaly caused by mutation in CENPJ']",0070290,608393,,C1842109,,,,C564247,,,,
mondo:0012030,autosomal dominant nonsyndromic hearing loss 43,"['autosomal dominant deafness 43', 'autosomal dominant nonsyndromic deafness type 43', 'deafness, autosomal dominant 43', 'autosomal dominant nonsyndromic deafness 43', 'DFNA43']",0110568,608394,,C1842108,,,,C564246,,,,
mondo:0012031,platelet-type bleeding disorder 10,"['platelet glycoprotein 4 deficiency', 'BDPLT10', 'CD36 inherited bleeding disorder, platelet-type', 'CD36 deficiency', 'platelet glycoprotein IV deficiency', 'bleeding disorder, Platelet-type, 10', 'inherited bleeding disorder, platelet-type caused by mutation in CD36']",0111046,608404,,C1842090,,,,C564245,,,,
mondo:0012032,Braddock syndrome,"['Vater-like syndrome with pulmonary hypertension, abnormal ears and growth deficiency', 'VATER-like defects with pulmonary hypertension, laryngeal webs, and growth deficiency']",,608406,52047,C4303988,,,,C564244,,,,
mondo:0012033,bradyopsia,"['bradyopsia', 'PERRS', 'prolonged electroretinal response suppression']",0070363,608415,75374,,"['-0.4832', '0.237', '-0.10205', '0.05145', '-0.0981', '-0.1606', '-0.0627', '0.435', '-0.0835', '-0.236', '-0.1309', '0.02223', '-0.08466', '0.05508', '0.134', '0.1866', '0.1025', '-0.03885', '-0.2573', '-0.4202', '-0.02774', '0.0323', '0.03357', '-0.1384', '-0.1079', '-0.0692', '-0.2413', '-0.02667', '-0.2266', '0.06903', '0.2666', '0.04742', '0.1482', '0.0931', '-0.1704', '-0.11395', '0.05856', '-0.2654', '-0.0867', '-0.0569', '0.2805', '-0.1192', '0.1699', '-0.28', '-0.1014', '0.02756', '-0.0702', '-0.275', '-0.12256', '0.1614', '-0.0669', '0.04724', '0.06854', '0.1945', '0.1472', '0.11096', '0.3552', '-0.2109', '-0.2386', '0.06195', '0.2474', '0.2445', '0.03516', '-0.003477', '0.0934', '-0.0143', '0.4124', '0.3127', '-0.1819', '0.1888', '-0.2313', '0.2423', '0.001294', '-0.1093', '0.2028', '0.2659', '-0.01211', '-0.2173', '0.10333', '-0.0823', '0.2104', '0.09845', '0.2361', '0.2898', '0.1831', '0.168', '0.11945', '0.1537', '0.3008', '-0.11816', '0.367', '0.4202', '-0.2046', '0.01604', '0.4856', '0.3386', '0.01776', '-0.3538', '0.0519', '0.2888']",,,C564243,368.8,,,
mondo:0012034,autosomal dominant limb-girdle muscular dystrophy type 1F,"['limb-girdle muscular dystrophy type 1F', 'muscular dystrophy limb-girdle type 1F', 'muscular dystrophy, limb-girdle, autosomal dominant 2', 'muscular dystrophy, limb-girdle, type 1F', 'LGMD1F']",0110304,608423,55595,,"['-0.01463', '-0.714', '-0.486', '-0.249', '0.4673', '-1.184', '0.4888', '0.838', '-1.578', '-0.78', '0.1635', '0.3875', '-0.3176', '1.221', '-0.04306', '0.3948', '-0.664', '-0.5215', '-0.807', '-0.793', '0.08954', '0.3032', '0.1207', '0.7974', '0.2646', '0.11847', '0.1338', '-0.6943', '0.4587', '-0.616', '1.036', '-0.02097', '0.4304', '0.12', '0.2433', '-0.0627', '-0.741', '0.12195', '-0.02109', '-0.253', '0.4165', '-0.1781', '-0.3', '0.5176', '-0.1508', '0.3865', '-0.04935', '0.737', '-0.338', '0.595', '0.3237', '-0.349', '0.3157', '-0.81', '0.3237', '-0.745', '0.3594', '0.6567', '-0.403', '-0.1187', '0.225', '-0.1006', '0.1411', '-0.08325', '-0.2302', '-0.0781', '0.1925', '0.3606', '-0.2703', '-0.2089', '-0.2578', '0.541', '0.3684', '-0.11926', '0.8213', '0.4475', '0.05722', '0.4233', '0.05872', '-0.04767', '0.05695', '-0.3103', '0.1818', '0.0662', '0.03772', '0.3108', '0.001089', '-0.176', '0.7812', '0.3562', '-0.2808', '-0.0852', '0.4106', '1.018', '0.05078', '-0.09314', '0.319', '-0.4927', '-0.0671', '-0.0641']",,,C564242,,,,
mondo:0012035,craniosynostosis-intracranial calcifications syndrome,"['Longman-Tolmie syndrome', 'craniosynostosis, calcification of basal ganglia, and facial dysmorphism']",,608432,52054,C1842058,,,,C564241,,,,
mondo:0012036,"systemic lupus erythematosus, susceptibility to, 4","['systemic lupus erythematosus, susceptibility to, 4', 'SLEB4']",,608437,,,,,,,,,,
mondo:0012037,"intellectual disability, autosomal recessive 3","['MRT3', 'intellectual disability, autosomal recessive 3', 'intellectual disability, autosomal recessive type 3', 'mental retardation, autosomal recessive 3', 'mental retardation, autosomal recessive type 3', 'autosomal recessive non-syndromic intellectual disability caused by mutation in CC2D1A', 'CC2D1A autosomal recessive non-syndromic intellectual disability']",0081179,608443,,C1838023,,,,C563929,,,,
mondo:0012038,speech-sound disorder,"['speech-sound disorder', 'SSD']",,608445,,C4078288,,,,C563928,,,,
mondo:0012039,"myocardial infarction, susceptibility to","['myocardial infarction, susceptibility to', 'myocardial infarction, protection against', 'myocardial infarction, decreased susceptibility to', 'myocardial infarction, susceptibility to, 1', 'susceptibility to myocardial infarction']",,608446,,,,,,,,,,
mondo:0012040,inflammatory bowel disease 9,"['inflammatory bowel disease type 9', 'inflammatory bowel disease 9', 'IBD9']",0110886,608448,,C1838019,,,,C563926,,,,
mondo:0012041,familial adenomatous polyposis 2,"['familial adenomatous polyposis 2', 'MUTYH-related attenuated FAP', 'MUTYH-associated polyposis', 'autosomal recessive multiple colorectal adenomas', 'MUTYH-related attenuated familial polyposis coli', 'MAP', 'MYH-associated polyposis', 'FAP2', 'MAP syndrome', 'MUTYH-related attenuated familial adenomatous polyposis', 'adenomas, multiple colorectal, autosomal recessive', 'autosomal recessive familial adenomatous polyposis', 'familial adenomatous polyposis, 2', 'familial adenomatous polyposis, type 2', 'colorectal adenomatous polyposis, autosomal recessive', 'MUTYH-related AFAP']",0080410,608456,247798,C1837991,"['0.3494', '0.365', '-0.4285', '0.1016', '-0.04288', '-0.4536', '-0.1362', '0.522', '-0.2852', '-0.08295', '0.4778', '0.333', '-0.166', '0.08466', '-0.205', '-0.3066', '-0.1203', '-0.2119', '0.4836', '-0.54', '0.05814', '0.1926', '-0.0631', '-0.2986', '0.6816', '-0.04413', '0.165', '0.143', '-0.0659', '-0.447', '0.5835', '-0.7397', '-0.04004', '-0.0332', '-0.1589', '0.237', '-0.21', '0.03653', '0.1821', '-0.0797', '0.3086', '-0.3904', '-0.38', '-0.1833', '-0.1425', '-0.1198', '-0.4124', '0.05286', '0.5444', '0.1364', '-0.04767', '-0.0329', '-0.2537', '0.07904', '-0.2241', '-0.3835', '-0.03052', '0.6816', '-0.928', '-0.05588', '0.7393', '0.06647', '0.607', '0.1616', '-0.2947', '0.5703', '0.51', '0.3938', '-0.7544', '0.343', '0.02478', '0.1746', '0.379', '0.03204', '0.1218', '0.06635', '0.056', '0.578', '-0.01013', '0.0852', '-0.4792', '0.2632', '0.0702', '-0.3984', '-0.4968', '-0.5635', '0.3638', '0.1171', '0.04095', '0.1459', '-0.1764', '-0.0578', '0.0705', '-0.18', '0.538', '-0.0977', '0.4026', '-0.6875', '-0.4143', '-0.0575']",C96520,,C563924,,,,
mondo:0012042,"Hirschsprung disease, susceptibility to, 8","['HSCR8', 'Hirschsprung disease, susceptibility to, 8']",,608462,,,,,,,,,,
mondo:0012043,Reis-Bucklers corneal dystrophy,"['geographic corneal dystrophy', 'CDB1', 'CDRB', 'granular corneal dystrophy type III', 'corneal dystrophy, geographic', 'superficial granular corneal dystrophy', 'corneal dystrophy of Bowman Layer, type 1', 'granular corneal dystrophy type 3', 'corneal dystrophy, REIS-Bucklers type', 'atypical granular corneal dystrophy', 'corneal dystrophy of Bowman layer type I', 'granular corneal dystrophy, type 3', 'Reis-Bücklers corneal dystrophy', 'anterior limiting membrane dystrophy type I', 'corneal dystrophy Reis Bucklers type', 'anterior limiting membrane dystrophy type 1', 'corneal dystrophy geographic', 'Reis Bucklers dystrophy', 'corneal dystrophy of Bowman layer type 1', 'RBCD', 'Reis-Bucklers corneal dystrophy', 'Reis Bucklers corneal dystrophy']",0060453,608470,98961,C0339278,"['-0.436', '-0.2368', '-0.8003', '0.02017', '0.3713', '-0.55', '-0.0676', '0.556', '-0.1746', '0.04416', '-0.0975', '-0.0661', '0.089', '0.7407', '-0.5303', '-0.3318', '0.5625', '-0.547', '0.1396', '-0.5596', '-0.592', '0.1547', '0.00517', '0.299', '-0.4114', '0.3892', '0.0961', '0.05283', '-0.666', '0.2372', '0.4783', '0.622', '0.1373', '0.158', '0.078', '0.3452', '-0.1592', '-0.6167', '0.2433', '-0.2712', '0.5854', '-0.614', '0.2788', '0.2722', '-0.2445', '0.431', '-0.3484', '-0.3113', '0.02406', '0.3364', '0.7476', '0.1604', '0.1925', '0.000773', '0.02281', '-0.0327', '0.4136', '0.242', '-0.5713', '-0.2507', '0.06464', '-0.256', '0.436', '0.259', '0.01132', '-0.2527', '1.025', '0.9126', '0.1279', '0.618', '-0.316', '-0.5625', '0.1642', '-0.219', '0.7085', '0.2756', '-0.2131', '0.3506', '-0.2852', '-0.5566', '0.1453', '-0.007557', '-0.02621', '0.06198', '0.154', '-0.922', '-0.3', '0.3096', '0.01852', '-0.143', '0.0916', '0.426', '0.08386', '0.3687', '0.1971', '0.2615', '0.3232', '-0.4841', '-0.246', '0.4956']",,,C535476,371.52,,,
mondo:0012044,"corneal dystrophy, lattice type 3A","['lattice corneal dystrophy type III A', 'CDL3A', 'corneal dystrophy, lattice type IIIA', 'lattice corneal dystrophy type 3A', 'lattice corneal dystrophy, type 3A']",,608471,,C1837974,,,,C563923,,,,
mondo:0012045,"myopia 5, autosomal dominant","['myopia 5, autosomal dominant', 'MYP5']",,608474,,C1837972,,,,C563922,,,,
mondo:0012046,"congenital corneal opacities, cornea guttata, and corectopia","['corneal opacities, congenital, with cornea guttata and corectopia', 'congenital corneal opacities, cornea guttata, and corectopia']",,608484,,C1837970,,,,C563921,,,,
mondo:0012047,"alopecia universalis congenita, 10Y gonadal dysgenesis, and laryngomalacia","['alopecia universalis congenita, XY gonadal dysgenesis, and laryngomalacia']",,608509,,C1837946,,,,C563920,,,,
mondo:0012048,endogenous depression,"['MDD', 'unipolar depression', 'clinical depression', 'major depressive disorder']",1595,,,,"['0.0676', '-0.01775', '-0.304', '0.5664', '-0.09595', '-0.488', '0.4749', '0.836', '-0.115', '-0.07355', '0.3066', '-0.1266', '-0.285', '0.281', '0.06216', '-0.12225', '-0.632', '-0.002872', '-0.952', '-0.6157', '-0.5903', '-0.2299', '0.3079', '-0.3533', '0.3704', '-0.43', '0.1313', '-0.1991', '0.332', '-0.576', '0.4436', '-0.3948', '0.2339', '0.3608', '-0.527', '0.42', '-0.621', '-0.06003', '0.2644', '-0.6235', '0.927', '0.0797', '-0.4077', '-0.1365', '0.8457', '-0.2542', '-0.2607', '-0.1812', '0.3105', '0.8022', '-0.1753', '0.4321', '0.1658', '0.03705', '0.827', '0.8057', '0.1436', '0.1929', '-0.3228', '-0.285', '-0.4417', '0.367', '-0.4905', '-0.1294', '-0.185', '0.8857', '-0.03214', '0.2147', '-0.5166', '0.3208', '0.2727', '0.08484', '0.201', '-1.104', '0.05905', '0.4204', '-0.0853', '0.6465', '-0.34', '-0.252', '0.4045', '-0.2021', '-0.4224', '-0.153', '0.3284', '-0.01619', '-0.03464', '-0.2817', '0.706', '0.2148', '-0.2128', '0.2642', '-0.3945', '0.1176', '0.1918', '0.5967', '-0.4668', '-0.634', '-0.457', '0.3887']",C35094,0003761,,,,,
mondo:0012049,orofaciodigital syndrome VII,"['orofaciodigital syndrome type VII', 'orofaciodigital syndrome VII', 'Whelan syndrome', 'oral-Facial-digital syndrome, type 7', 'OFD7', 'Ofds 7', 'orofaciodigital syndrome type 7', 'orofaciodigital syndrome 7']",0060377,608518,90649,CN206429,,,,C563104,,,,
mondo:0012050,major depressive disorder 1,"['major depressive disorder 1', 'major depressive disorder type 1', 'MDD1', 'unipolar depression 1']",,608520,,C1837929,,,,C563919,,,,
mondo:0012051,"periodontitis, aggressive, 2","['periodontitis, aggressive, 2', 'periodontitis, aggressive, type 2']",,608526,,C1969478,,,,C566946,,,,
mondo:0012052,ALG1-congenital disorder of glycosylation,"['ALG1-CDG (CDG-Ik)', 'CDG1K', 'ALG1-CDG', 'CDG 1K', 'CDG Ik', 'CDG-Ik', 'mannosyltransferase 1 deficiency', 'CDG syndrome type Ik', 'congenital disorder of glycosylation type 1k', 'carbohydrate deficient glycoprotein syndrome type Ik', 'congenital disorder of glycosylation, type Ik', 'congenital disorder of glycosylation type Ik']",0080563,608540,79327,C2931005,"['-0.276', '-0.0405', '0.0442', '-0.633', '-0.252', '-0.6016', '0.05106', '0.1512', '-0.2856', '-0.1393', '-0.1932', '-0.484', '-0.01501', '-0.2505', '-0.5386', '-0.166', '0.233', '-0.07745', '-0.088', '-0.5005', '0.3762', '-0.3984', '-0.02336', '0.1757', '0.2544', '0.01564', '0.0715', '0.1792', '0.2678', '-0.2056', '0.4436', '0.3372', '1.208', '0.3533', '-0.0928', '0.109', '-0.4434', '0.2047', '-0.4246', '-0.5107', '-0.2101', '-0.1635', '0.2482', '0.0233', '-0.01104', '0.0794', '-0.0692', '0.289', '0.4033', '0.0632', '-0.2966', '0.2754', '0.2847', '0.177', '-0.1125', '-0.1847', '0.0475', '0.0717', '-0.3196', '0.4807', '-0.0336', '-0.05875', '0.371', '-0.2179', '-0.07275', '-0.4429', '0.2852', '0.1338', '-0.6533', '0.1906', '-0.6772', '0.3564', '0.1261', '0.2422', '-0.0104', '-0.09436', '0.814', '-0.1096', '-0.127', '0.5547', '-0.08606', '0.02806', '-0.2693', '0.2438', '0.0871', '0.181', '0.2878', '0.684', '0.3416', '0.3416', '-0.01204', '0.7183', '0.1428', '-0.1835', '0.3142', '0.705', '0.4468', '-0.1309', '0.00536', '0.3452']",,,C535749,,,,
mondo:0012053,"aneurysm, intracranial berry, 2","['ANIB2', 'aneurysm, intracranial BERRY, 2']",0080965,608542,,C1837894,,,,C536360,,,,
mondo:0012054,schizophrenia 12,"['Sczd12', 'SCZD12', 'schizophrenia type 12', 'schizophrenia susceptibility locus, chromosome 1P-related', 'schizophrenia 12']",0070088,608543,,C1837893,,,,,,,,
mondo:0012055,Larsen-like osseous dysplasia-short stature syndrome,"['Larsen-like syndrome', 'Lrsl', 'Larsen-like syndrome, isolated cases']",,608545,2370,C1837884,,,,C563914,,,,
mondo:0012056,Leber congenital amaurosis 9,"['NMNAT1 Leber congenital amaurosis', 'Leber congenital amaurosis type 9', 'amaurosis congenita of Leber, type 9', 'LCA9', 'Leber congenital amaurosis caused by mutation in NMNAT1', 'Leber congenital amaurosis 9']",0110005,608553,,,,,,C536603,,H35.5,,
mondo:0012057,"legionnaire disease, susceptibility to","['Legionella infection', 'susceptibility to legionnaire disease', 'legionnaire^s disease', 'legionnaire disease, susceptibility to']",,608556,,,"['-0.02615', '0.04352', '0.02196', '-0.01822', '0.03644', '-0.08856', '0.0194', '0.04443', '-0.04132', '-0.06097', '-0.00222', '0.02408', '-0.004684', '0.01761', '-0.01037', '-0.05487', '0.01491', '-0.03726', '-0.02652', '-0.1174', '0.02684', '-0.02628', '0.0784', '-0.00206', '-0.02025', '-0.01785', '-0.0329', '0.01254', '-0.02263', '-0.04855', '0.0532', '-0.01276', '0.07', '-0.002728', '0.02394', '-0.02797', '-0.0295', '-0.01698', '-0.00453', '-0.0484', '0.01903', '-0.03238', '0.04056', '-0.0308', '-0.01006', '-0.0863', '0.01869', '0.03238', '0.01055', '0.02007', '-0.02821', '-0.02701', '0.0424', '0.012856', '-0.00942', '-0.02495', '0.0389', '-0.03348', '-0.059', '0.01296', '0.02861', '0.02953', '-0.01204', '0.02737', '0.03061', '0.04266', '0.0629', '0.0611', '-0.06476', '0.087', '-0.05582', '-0.004814', '0.005352', '-0.04703', '0.02483', '0.04416', '-0.00505', '-0.00596', '-0.01584', '-0.006664', '-0.02173', '-0.01248', '-0.01515', '0.0863', '-0.004147', '-0.01186', '0.04578', '0.06024', '0.0672', '0.001378', '0.01924', '0.063', '-0.00894', '0.009796', '0.1278', '0.0688', '0.06238', '-0.0672', '-0.0287', '0.0015745']",,,,,,,
mondo:0012058,"myocardial infarction, susceptibility to, 2","['Mci2', 'myocardial infarction, susceptibility to, 2', 'myocardial infarction, susceptibility to, type 2']",,608557,,C1837871,,,,,,,,
mondo:0012059,"polydactyly, postaxial, type A4","['polydactyly, postaxial, type A4', 'postaxial polydactyly, type A4', 'Papa4']",,608562,,C1837868,,,,C563909,,,,
mondo:0012060,autosomal recessive nonsyndromic hearing loss 35,"['autosomal recessive nonsyndromic deafness caused by mutation in ESRRB', 'ESRRB autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 35', 'autosomal recessive deafness 35', 'deafness, autosomal recessive type 35', 'autosomal recessive nonsyndromic deafness 35', 'deafness, autosomal recessive 35', 'DFNB35']",0110493,608565,,C1837857,,,,C563908,,,,
mondo:0012061,familial sick sinus syndrome,"['familial sinus node dysfunction', 'sick sinus syndrome 1, autosomal recessive', 'SSS1', 'hereditary sick sinus syndrome']",,,166282,,"['0.2325', '0.3684', '0.4646', '0.4578', '-0.3616', '0.4546', '0.8247', '0.94', '-0.1052', '-0.1687', '0.312', '-0.01549', '-0.355', '0.6177', '-0.2766', '0.3994', '-0.609', '0.0647', '-0.3708', '-0.3699', '0.3862', '0.2207', '0.5464', '0.2722', '0.2817', '-1.073', '0.04068', '0.03183', '0.5215', '0.5166', '0.4194', '0.606', '0.531', '0.2695', '-0.1892', '-0.3525', '0.3582', '0.2235', '0.05', '-0.4138', '0.3318', '0.323', '0.1528', '0.1624', '0.591', '0.1593', '-0.568', '-0.05505', '0.5156', '0.03278', '-0.1473', '0.2969', '-0.3474', '-0.2515', '-0.53', '-0.657', '-0.5396', '0.3057', '-0.6655', '-0.1406', '0.06824', '0.7983', '-0.01239', '-0.1858', '-0.2073', '0.0754', '0.4106', '1.107', '-0.2847', '0.06445', '-0.5703', '0.412', '0.11', '-0.2382', '0.1512', '0.603', '-0.08716', '0.4521', '-0.4158', '0.1882', '-0.172', '-0.42', '-0.1239', '-0.10315', '0.346', '-0.05737', '1.14', '0.1176', '0.4253', '0.5303', '0.2605', '-0.0702', '-0.1968', '0.4216', '0.6895', '0.545', '0.0889', '-0.2151', '-0.951', '-0.1147']",,,C563907,,,10040639,
mondo:0012062,dilated cardiomyopathy 1O,"['dilated cardiomyopathy type 1O', 'cardiomyopathy, dilated, with ventricular tachycardia', 'cardiomyopathy, dilated, type 1O', 'dilated cardiomyopathy with ventricular tachycardia', 'familial isolated dilated cardiomyopathy caused by mutation in ABCC9', 'cardiomyopathy, dilated, 1O', 'ABCC9 familial isolated dilated cardiomyopathy', 'CMD1O']",0110451,608569,,C1837839,,,,C563906,,,,
mondo:0012063,ulnar/fibula ray defect-brachydactyly syndrome,"['ulnar/fibular RAY defect and brachydactyly', 'Morava-Mehes syndrome']",,608571,52056,,,,,C563905,,,,
mondo:0012064,choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome,"['bilateral choanal atresia, cardiac defects, deafness, and dysmorphic appearance', 'BMKS', 'Burn-McKeown syndrome', 'oculootofacial dysplasia', 'choanal atresia deafness cardiac defects dysmorphism']",0080695,608572,1200,C1835913,"['0.581', '0.1761', '0.2512', '0.0767', '-0.4812', '0.212', '0.872', '0.8833', '-0.1212', '-0.8354', '0.6216', '0.01349', '-0.326', '0.3994', '-0.6147', '-0.4553', '-1.077', '0.1396', '-0.3538', '-0.2275', '0.3176', '0.2825', '-0.475', '0.358', '0.9834', '0.1032', '-1.362', '0.1732', '-0.0898', '0.064', '0.0627', '-0.183', '0.2822', '-0.09393', '-0.1764', '-0.616', '-0.2864', '-0.556', '0.03995', '-0.4734', '0.1613', '-0.06015', '0.1173', '-0.67', '0.039', '-0.3523', '-0.0672', '0.5264', '-0.3547', '-0.1929', '-0.283', '-0.667', '-0.175', '-0.1549', '0.04025', '0.3196', '-0.1484', '-0.02249', '0.0733', '0.06683', '-0.26', '0.9424', '-0.4958', '0.4397', '-0.6177', '-0.1437', '-0.2795', '0.9956', '-0.3171', '-0.262', '0.1656', '0.747', '0.918', '-0.78', '-0.086', '-0.205', '1.139', '-0.0746', '-0.1583', '-0.2173', '0.4229', '-0.7026', '-0.406', '0.6313', '0.08276', '-0.531', '-0.1229', '1.19', '-0.1835', '0.6367', '0.2815', '0.4976', '0.2028', '0.7944', '0.597', '-0.2605', '0.0557', '-0.989', '-0.08765', '-0.10834']",,,C563682,,,,
mondo:0012066,"atrial fibrillation, familial, 1","['atrial fibrillation, autosomal dominant', 'ATFB1', 'atrial fibrillation, familial, 1']",,608583,,C1843687,,,,C538261,,,,
mondo:0012067,"asthma-related traits, susceptibility to, 2","['inherited susceptibility to asthma caused by mutation in NPSR1', 'asthma, susceptibility to, 2', 'NPSR1 inherited susceptibility to asthma', 'asthma-related traits, susceptibility to, 2', 'asthma-related traits, susceptibility to, type 2', 'ASRT2']",,608584,,C1837811,,,,,,,,
mondo:0012068,"brachial palsy, familial congenital","['brachial palsy, familial congenital']",,608585,,C1837810,,,,C563901,,,,
mondo:0012069,keratoconus 3,"['keratoconus 3', 'KTCN3']",,608586,,C1837809,,,,C563900,,,,
mondo:0012071,congenital generalized lipodystrophy type 1,"['lipodystrophy, congenital generalized, type 1', 'Brunzell syndrome, AGPAT2-related', 'BSCL1', 'Berardinelli-Seip congenital lipodystrophy, type 1', 'Berardinelli-Seip congenital lipodystrophy type 1', 'AGPAT2 congenital generalised lipodystrophy (disease)', 'CGL1', 'congenital generalised lipodystrophy (disease) caused by mutation in AGPAT2', 'AGPAT2 congenital generalized lipodystrophy (disease)', 'AGPAT2-related Brunzell syndrome', 'lipodystrophy, Berardinelli-Seip congenital, type 1', 'Brunzell syndrome AGPAT2-related']",0111135,608594,,,,,,,,,,
mondo:0012072,"familial partial lipodystrophy, Kobberling type","['lipodystrophy, familial partial, type 1', 'familial partial lipodystrophy, Köbberling type', 'lipodystrophy, familial partial, Kobberling type', 'familial partial lipodystrophy type 1', 'familial partial lipodystrophy type Köbberling', 'FPLD1']",0070207,608600,79084,,,,,,,,,
mondo:0012073,ribose-5-P isomerase deficiency,['ribose 5-phosphate isomerase deficiency'],,608611,440706,C1291609,,,,C563212,277.6,,,
mondo:0012074,mandibuloacral dysplasia with type B lipodystrophy,"['lipodystrophy, type B, associated with Mandibuloacral dysplasia', 'mandibuloacral dysplasia with type B lipodystrophy', 'MANDIBULOACRAL dysplasia with type B lipodystrophy', 'MADB']",0081129,608612,90154,C1837756,"['-0.0468', '0.11346', '0.09534', '-0.06232', '0.10944', '-0.1678', '0.0504', '0.08856', '-0.0826', '-0.0691', '-0.1111', '-0.0369', '-0.006615', '0.01531', '-0.0958', '-0.02768', '0.0698', '-0.04312', '-0.04083', '-0.2141', '-0.001259', '-0.05838', '0.1898', '-0.0272', '0.04434', '0.002731', '-0.005795', '-0.06155', '0.00785', '-0.1293', '0.1202', '0.01187', '0.1345', '0.04724', '0.10254', '-0.06616', '-0.03397', '-0.05768', '-0.06793', '-0.154', '-0.04053', '-0.1439', '-0.03574', '0.00803', '-0.06125', '-0.123', '-0.04495', '0.1334', '0.0385', '-0.03156', '0.01834', '-0.058', '0.0614', '0.03177', '-0.156', '-0.06604', '0.05167', '-0.1539', '-0.2229', '-0.02187', '0.03958', '0.03065', '-0.02681', '-0.012695', '0.00411', '0.01318', '0.153', '0.03662', '-0.10205', '0.1259', '-0.1343', '-0.02068', '0.06586', '-0.09827', '0.09326', '0.02766', '-0.05698', '-0.02266', '-0.07874', '-0.0733', '-0.02655', '0.02777', '-0.02022', '0.09064', '-0.0595', '0.013855', '0.06726', '0.2113', '0.1451', '0.005558', '0.04034', '0.108', '0.03925', '0.04266', '0.2245', '0.03287', '0.133', '-0.2206', '-0.03064', '0.0786']",,,C535706,,,,
mondo:0012075,oligodontia-cancer predisposition syndrome,"['autosomal dominant ectodermal dysplasia-cancer predisposition syndrome', 'tooth agenesis-colorectal cancer syndrome', 'ODCRCS', 'oligodontia-colorectal cancer syndrome']",,608615,300576,C1837750,"['0.2284', '-0.0296', '0.0461', '0.4736', '0.851', '-0.9937', '0.626', '0.575', '-0.05493', '0.02281', '0.8', '-0.00983', '-0.2761', '0.5464', '-0.3926', '-0.4275', '-0.11993', '-0.622', '-0.868', '-0.4753', '-0.05618', '-0.689', '-0.5605', '-0.1617', '0.3933', '-0.6167', '0.2194', '0.08765', '0.4644', '-0.005432', '0.5312', '-0.483', '0.1674', '-0.8975', '0.941', '-0.1294', '-1.073', '0.127', '-0.2573', '-0.11414', '0.419', '-0.1289', '0.01974', '-0.03442', '-0.0713', '0.0013', '-0.2028', '-0.9556', '1.528', '-0.4534', '-0.1384', '-0.4163', '0.076', '-0.216', '-0.3772', '0.10455', '-0.3623', '0.0948', '-1.194', '-0.936', '0.6484', '0.1164', '-0.2708', '-0.53', '-0.4263', '0.6006', '0.442', '0.317', '0.06024', '0.935', '-0.0784', '0.9043', '0.00882', '-0.11426', '1.2295', '0.3315', '-0.07465', '0.11096', '0.1788', '0.51', '-0.08905', '0.2542', '-0.0519', '0.1251', '0.1694', '-0.08075', '0.7524', '0.4446', '0.771', '-0.5547', '-0.02573', '0.1368', '-0.07635', '0.506', '0.04333', '0.3423', '-0.339', '-0.722', '-0.3972', '-0.1643']",,,C563898,,,,
mondo:0012076,"midface hypoplasia, obesity, developmental delay, and neonatal hypotonia","['midface hypoplasia, obesity, developmental delay, and neonatal hypotonia']",,608624,,C1837730,,,,C563896,,,,
mondo:0012077,amyotrophic lateral sclerosis type 8,"['ALS8', 'amyotrophic lateral sclerosis caused by mutation in VAPB', 'amyotrophic lateral sclerosis 8', 'amyotrophic lateral sclerosis type 8', 'VAPB amyotrophic lateral sclerosis']",0050752,608627,,,,,,C563895,,,,
mondo:0012078,Joubert syndrome 3,"['JBTS3', 'Joubert syndrome 3', 'AHI1 Joubert syndrome', 'Joubert syndrome caused by mutation in AHI1', 'Joubert syndrome type 3']",0110998,608629,,C1837713,,C148259,,C536295,,,,
mondo:0012079,"asperger syndrome, susceptibility to, 2","['ASPG2', 'Asperger syndrome susceptibility 2, Isolated cases', 'ASPERGER syndrome, susceptibility to, 2']",,608631,,C1837697,,,,,,,,
mondo:0012080,"neuronopathy, distal hereditary motor, type 2B","['neuropathy, distal hereditary motor, type 2B', 'HSPB1 neuronopathy, distal hereditary motor', 'HMN 2B', 'neuronopathy, distal hereditary motor, type IIB', 'neuronopathy, distal hereditary motor caused by mutation in HSPB1', 'HMN2B']",0111207,608634,,C2608087,,,,C567084,,,,
mondo:0012081,15q11q13 microduplication syndrome,"['Duplication 15Q11-q13 syndrome', '15q11q13 duplication syndrome', '15q11-q13 microduplication syndrome', 'autism, susceptibility to, 4', 'trisomy 15q11q13', 'chromosome 15q11-q13 DUPLICATION syndrome', 'trisomy 15q11-q13', 'dup(15)(q11q13)', 'chromosome 15Q11.2 Duplication syndrome', 'autism susceptibility 4', '15q11-q13 duplication syndrome']",,608636,238446,C4304726,,C126692,,,,,,
mondo:0012082,"asperger syndrome, susceptibility to, 1","['Asperger syndrome susceptibility 1, Isolated cases', 'ASPERGER syndrome, susceptibility to, 1', 'ASPG1']",,608638,,C1837646,,,,,,,,
mondo:0012083,autosomal dominant nonsyndromic hearing loss 28,"['autosomal dominant nonsyndromic deafness type 28', 'deafness, autosomal dominant 28', 'GRHL2 autosomal dominant nonsyndromic deafness', 'autosomal dominant nonsyndromic deafness 28', 'deafness, autosomal dominant type 28', 'DFNA28', 'autosomal dominant nonsyndromic deafness caused by mutation in GRHL2', 'autosomal dominant deafness 28']",0110557,608641,,C1837640,,,,C563890,,,,
mondo:0012084,aromatic L-amino acid decarboxylase deficiency,"['aromatic L-amino acid decarboxylase deficiency', 'aromatic L-amino-acid decarboxylase deficiency', 'Aadc deficiency', 'aromatic amino acid decarboxylase deficiency', 'DDC deficiency', 'AADC deficiency', 'Dopa decarboxylase deficiency']",0090123,608643,35708,,"['-0.623', '0.4355', '-0.0149', '-0.08234', '-0.1605', '-0.4668', '0.2068', '0.7446', '-0.508', '-0.194', '0.09204', '0.5884', '-0.10815', '0.05838', '0.3037', '-0.0319', '-0.0718', '-0.133', '-0.5083', '-0.669', '-0.0348', '-0.1512', '0.268', '-0.03366', '-0.1969', '-0.2651', '0.2954', '0.1827', '-0.4502', '-0.594', '0.564', '0.6245', '1.1045', '0.632', '-0.1844', '-0.3643', '-0.2913', '-0.5254', '-0.3474', '0.003384', '0.2444', '-0.1024', '-0.1377', '0.1146', '0.5127', '-0.3684', '-0.2754', '-0.2432', '-0.2703', '0.7456', '-1.163', '0.3484', '-0.4382', '0.04077', '-0.09283', '0.2063', '0.3547', '-0.02132', '0.1703', '0.0866', '0.4958', '0.3218', '0.865', '-0.1015', '0.3535', '0.2754', '0.1505', '-0.05487', '-0.3237', '0.04254', '-0.2944', '-0.3723', '-0.275', '0.4011', '0.6533', '0.9707', '0.4639', '-0.2361', '0.1909', '0.6377', '0.8247', '-0.515', '0.09375', '0.704', '0.451', '1.059', '-0.3132', '0.1559', '0.91', '0.3223', '0.5728', '0.1328', '-0.12164', '-0.0004432', '0.2764', '0.4832', '0.1111', '-0.1619', '0.2524', '-0.1312']",C142085,,C537437,270.8,,,
mondo:0012085,primary ciliary dyskinesia 3,"['ciliary dyskinesia, primary, type 3', 'primary ciliary dyskinesia type 3', 'ciliary dyskinesia, primary, 3', 'ciliary dyskinesia, primary, 3, with or without situs inversus', 'primary ciliary dyskinesia caused by mutation in DNAH5', 'primary ciliary dyskinesia 3 with or without situs inversus', 'CILD3', 'DNAH5 primary ciliary dyskinesia']",0110599,608644,,C1837618,,C172392,,C535278,,,,
mondo:0012086,autosomal dominant nonsyndromic hearing loss 31,"['autosomal dominant deafness 31', 'deafness, autosomal dominant 31', 'autosomal dominant nonsyndromic deafness type 31', 'DFNA31', 'autosomal dominant nonsyndromic deafness 31']",0110561,608645,,C1837617,,,,C563888,,,,
mondo:0012087,primary ciliary dyskinesia 4,"['ciliary dyskinesia, primary, 4, with or without situs inversus', 'CILD4', 'ciliary dyskinesia, primary, 4', 'primary ciliary dyskinesia type 4', 'primary ciliary dyskinesia 4 with or without situs inversus']",0110614,608646,,C1837616,,,,C535279,,,,
mondo:0012088,primary ciliary dyskinesia 5,"['ciliary dyskinesia, primary, 5, without situs inversus', 'primary ciliary dyskinesia caused by mutation in HYDIN', 'ciliary dyskinesia, primary, 5', 'primary ciliary dyskinesia type 5', 'HYDIN primary ciliary dyskinesia', 'ciliary dyskinesia, primary, type 5', 'CILD5', 'primary ciliary dyskinesia 5 without situs inversus']",0110617,608647,,C1837615,,,,C563886,,,,
mondo:0012089,ichthyosis prematurity syndrome,"['congenital ichthyosis type 4', 'IPS', 'ichthyosis congenita 4', 'ichthyosis congenita IV', 'idiopathic pneumonia syndrome', 'ichthyosis-prematurity syndrome', 'ichthyosis prematurity syndrome']",,608649,88621,C1837610,"['-0.1498', '0.11615', '-0.305', '-0.03674', '0.1931', '-0.3677', '0.05243', '-0.03079', '-0.03632', '-0.04047', '-0.0201', '0.3027', '-0.2385', '-0.2637', '-0.1875', '-0.11224', '0.2356', '0.0601', '0.003199', '-0.6836', '-0.0959', '-0.1973', '0.5576', '-0.3804', '0.151', '0.1575', '-0.02979', '0.4944', '-0.1186', '-0.1893', '0.1676', '-0.09106', '0.4858', '0.2864', '0.06055', '0.3362', '-0.1931', '-0.2632', '-0.3022', '-0.0817', '-0.1995', '-0.157', '0.04022', '0.02554', '-0.4036', '0.0875', '-0.3499', '0.197', '0.1101', '0.2263', '-0.2487', '-0.2505', '0.0916', '-0.04202', '-0.478', '-0.1426', '-0.01324', '-0.2196', '-0.1658', '-0.1779', '0.1986', '0.171', '-0.1758', '-0.003317', '0.32', '-0.1376', '0.4905', '0.2223', '-0.5044', '0.6323', '-0.2886', '0.02243', '-0.0658', '0.3381', '-0.4294', '-0.1145', '0.4126', '-0.2063', '-0.1421', '-0.1593', '-0.3584', '0.2325', '-0.4229', '-0.11127', '0.0324', '0.0523', '0.2886', '0.612', '0.2952', '-0.01231', '0.6562', '0.1821', '-0.01396', '0.2952', '0.2695', '-0.02592', '0.1284', '-0.306', '0.2198', '-0.1328']",C62590,,C536271,,,,
mondo:0012090,autosomal dominant nonsyndromic hearing loss 47,"['autosomal dominant deafness 47', 'deafness, autosomal dominant 47', 'autosomal dominant nonsyndromic deafness 47', 'autosomal dominant nonsyndromic deafness type 47', 'DFNA47']",0110570,608652,,C1837609,,,,C563885,,,,
mondo:0012091,autosomal recessive nonsyndromic hearing loss 32,"['DFNB32', 'autosomal recessive nonsyndromic deafness 32', 'deafness, autosomal recessive 105', 'autosomal recessive nonsyndromic deafness type 105', 'DFNB105', 'deafness, autosomal recessive type 105', 'autosomal recessive deafness 105', 'autosomal recessive deafness 32', 'autosomal recessive nonsyndromic deafness 105', 'deafness, autosomal recessive 32', 'autosomal recessive nonsyndromic deafness caused by mutation in CDC14A', 'deafness, autosomal recessive 32, with or without immotile sperm', 'CDC14A autosomal recessive nonsyndromic deafness', 'autosomal recessive nonsyndromic deafness type 32']",0110491,608653,,C4310777,,,,C563884,,,,
mondo:0012092,hereditary sensory and autonomic neuropathy type 5,"['HSAN 5', 'neuropathy, hereditary sensory and autonomic, type 5', 'HSAN5', 'hereditary sensory and autonomic neuropathy type V', 'autosomal recessive hereditary sensory and autonomic neuropathy caused by mutation in NGF', 'insensitivity to pain, congenital', 'NGF autosomal recessive hereditary sensory and autonomic neuropathy', 'congenital insensitivity to pain and thermal analgesia', 'HSAN V', 'neuropathy, hereditary sensory and autonomic, type V']",0070145,608654,64752,,"['0.5864', '-0.149', '-0.4185', '0.4287', '-0.1979', '-0.4297', '-0.3533', '0.4946', '-0.333', '0.0822', '0.1151', '0.4658', '0.2308', '0.4663', '-0.62', '0.47', '-0.1616', '0.8926', '-0.873', '-0.912', '0.2559', '0.066', '-0.525', '0.3245', '0.01411', '0.0843', '-0.7134', '0.1117', '-0.22', '-0.3857', '0.843', '-0.2805', '0.1189', '-0.1345', '-0.433', '-0.2605', '0.2964', '-0.0687', '-0.0929', '-0.2686', '-0.5347', '-0.2732', '-0.004036', '-0.1455', '0.3313', '-0.323', '0.3186', '-0.1192', '0.1791', '0.07404', '-0.418', '1.079', '0.2927', '-1.011', '0.1235', '0.521', '0.4766', '0.2512', '-0.5356', '-0.3926', '0.3252', '0.6733', '0.3572', '0.4392', '-0.10657', '0.712', '0.4375', '0.414', '-0.1963', '0.12036', '-1.067', '0.273', '-0.5723', '-0.1663', '0.7207', '0.538', '0.3618', '0.913', '-0.6636', '0.706', '-0.0558', '-0.6914', '0.4834', '0.3276', '-0.02158', '-0.2407', '0.464', '0.3276', '0.395', '-0.3364', '0.3733', '0.2632', '0.35', '-0.1986', '1.071', '0.7246', '-0.2017', '-0.306', '0.267', '0.345']",,,,,,,
mondo:0012093,"prostate cancer, hereditary, 3","['HPC3', 'prostate cancer, hereditary, type 3', 'prostate cancer, susceptibility to, 3', 'prostate cancer, hereditary, 3']",,608656,,C1837595,,,,C563883,,,,
mondo:0012094,"prostate cancer, hereditary, 4","['HPC4', 'prostate cancer, hereditary, type 4', 'prostate cancer, susceptibility to, 4', 'prostate cancer, hereditary, on chromosome 7', 'prostate cancer, hereditary, 4']",,608658,,C1837593,,,,C563882,,,,
mondo:0012095,intellectual disability-brachydactyly-Pierre Robin syndrome,['ROBIN sequence with distinctive facial appearance and brachydactyly'],,608670,364577,C1837564,,,,C563880,,,,
mondo:0012096,Charcot-Marie-Tooth disease axonal type 2L,"['Charcot-Marie-Tooth disease, axonal, type 2L', 'Charcot-Marie-Tooth disease type 2L', 'Charcot-Marie-Tooth neuropathy, axonal, type 2L', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2L', 'Charcot-Marie-Tooth disease type 2 caused by mutation in HSPB8', 'Charcot-Marie-Tooth neuropathy axonal type 2L', 'autosomal dominant axonal Charcot-Marie-Tooth disease type 2L', 'CMT2L', 'autosomal dominant Charcot-Marie-Tooth disease type 2L', 'HSPB8 Charcot-Marie-Tooth disease type 2']",0110174,608673,99945,C4304673,"['0.4224', '0.2133', '0.04565', '0.03204', '0.2428', '-0.4355', '0.01147', '0.8247', '-0.486', '-0.3008', '-0.127', '0.46', '-0.6016', '0.1688', '-0.0831', '-0.02888', '-0.1654', '-0.694', '-0.583', '-0.657', '0.02145', '0.4329', '-0.1181', '0.2898', '0.2634', '0.1454', '0.1095', '0.2004', '-0.0713', '0.03638', '0.09686', '-0.585', '0.1215', '0.2368', '0.4368', '-1.079', '-0.472', '-0.3625', '0.3247', '-0.0371', '-1.564', '-0.493', '-0.2622', '0.04813', '0.05356', '-0.282', '0.09546', '-0.3623', '-0.3298', '-0.0879', '0.3577', '0.4856', '-0.5767', '-1.196', '0.4028', '0.2262', '-0.1985', '0.3105', '-0.9263', '-0.09424', '-0.2123', '-0.2869', '0.7583', '0.555', '-0.8306', '0.924', '-0.1425', '0.8325', '-0.5913', '0.4104', '-0.4329', '-0.0873', '0.4702', '-0.2437', '1.328', '0.8667', '-0.02602', '0.3062', '0.128', '-0.3884', '-0.1337', '-0.4004', '1.2295', '0.7524', '0.1532', '-0.2456', '0.16', '0.558', '0.4946', '0.1873', '0.4368', '-0.1842', '-0.1897', '0.4536', '0.682', '0.519', '0.5493', '-0.672', '-0.05664', '0.633']",,,,,,,
mondo:0012097,"spondylocostal dysostosis 2, autosomal recessive","['spondylocostal dysostosis 2, autosomal recessive', 'spondylocostal dysostosis 2', 'SCDO2']",0112362,608681,,C1837549,,,,,,,,
mondo:0012098,spinocerebellar ataxia type 20,"['chromosome 11q12 duplication syndrome, 260-Kb', 'spinocerebellar ataxia with spasmodic cough', 'spinocerebellar ataxia 20', 'spinocerebellar ataxia with dysphonia', 'SCA20', 'spinocerebellar ataxia type 20']",0050971,608687,101110,C1837541,"['-0.01283', '-0.2166', '-0.0996', '0.10583', '-0.3323', '-1.01', '0.2236', '0.3145', '-0.5674', '-0.9126', '0.06354', '0.2258', '-0.148', '0.079', '0.6704', '-0.2168', '-0.1503', '-0.4375', '0.1956', '-0.861', '-0.2974', '-0.2324', '0.1522', '-0.6787', '0.4954', '-0.4758', '-0.3083', '0.2269', '-0.2244', '-0.8315', '0.2092', '0.4275', '-0.4846', '-0.223', '0.4207', '0.04675', '-0.0702', '0.165', '0.3518', '0.4956', '0.3862', '0.249', '-0.5557', '0.351', '0.538', '-0.6104', '0.010635', '0.4111', '0.1437', '0.07117', '-0.08545', '-0.02013', '-0.013504', '-0.5005', '0.04065', '-0.821', '0.3657', '0.3645', '0.1137', '0.3035', '-0.5537', '0.4016', '0.1609', '-0.1233', '-0.293', '0.4856', '0.355', '0.804', '-0.7', '0.5547', '0.7847', '0.4688', '-0.04282', '-0.637', '0.65', '0.357', '0.2812', '0.1338', '0.09406', '0.4558', '-0.3408', '-0.912', '0.4575', '0.574', '-0.387', '-0.5938', '0.2866', '0.01227', '0.5435', '0.4429', '0.5415', '0.291', '-0.093', '-0.05127', '1.059', '0.8037', '0.3723', '0.4695', '-0.3232', '-0.06104']",,,C537199,,,,
mondo:0012099,AICA-ribosiduria,"['Atic deficiency', 'AICA-ribosiduria due to ATIC deficiency', 'AICAR transformylase/IMP cyclohydrolase deficiency', 'ATIC deficiency', 'Aica-Ribosuria due to Atic deficiency', '5-amino-4-imidazole carboxamide ribosiduria']",,608688,250977,C4510943,"['0.05014', '-0.066', '-0.289', '-0.1378', '0.2583', '-0.8687', '0.2225', '0.65', '-1.234', '-0.277', '0.02289', '0.411', '0.534', '-0.131', '0.1824', '-0.11896', '0.255', '-0.07153', '-0.572', '-0.7065', '0.3372', '0.3152', '0.5796', '0.6255', '-0.1656', '0.05557', '-0.09955', '0.788', '0.374', '-0.01364', '0.06003', '-0.2495', '0.528', '0.2783', '-0.4685', '-0.003813', '-0.00647', '-0.2769', '-0.0759', '0.241', '0.2524', '-0.1081', '0.0323', '-0.4446', '0.3389', '0.6743', '-0.2266', '-0.641', '-0.541', '0.2003', '-0.2355', '-0.4307', '0.02963', '0.354', '-0.1724', '-0.1635', '0.5923', '-0.3923', '-0.1062', '0.1394', '0.07874', '-0.4805', '-0.0834', '0.1453', '0.1326', '-0.3901', '0.464', '0.58', '-0.307', '0.257', '-0.2218', '-0.2096', '-0.5664', '-0.079', '-0.392', '0.06323', '0.2654', '-0.1927', '-0.328', '0.3762', '1.068', '0.563', '-0.531', '0.8066', '-0.0215', '0.664', '-0.06757', '0.3884', '0.922', '0.74', '0.2913', '0.173', '-0.5503', '-0.1226', '0.4573', '0.2915', '0.4233', '-0.2705', '0.7524', '0.128']",,,C563876,,,,
mondo:0012100,major depressive disorder 2,"['MDD2', 'major depressive disorder 2', 'unipolar depression 2', 'major depressive disorder type 2']",,608691,,C1837529,,,,C563875,,,,
mondo:0012101,"glaucoma 1, open angle, J","['JOAG2', 'JOAG1J', 'glaucoma, primary open angle, juvenile-onset, 2', 'glaucoma 1, open angle, J', 'GLC1J']",,608695,,C1837528,,,,C563874,,,,
mondo:0012102,"glaucoma 1, open angle, K","['glaucoma 1K, primary open angle, juvenile-onset', 'GLC1K', 'glaucoma, primary open angle, juvenile-onset, 3', 'JOAG1K', 'glaucoma 1, open angle, K']",,608696,,C1837527,,,,C563873,,,,
mondo:0012103,spinocerebellar ataxia type 25,"['spinocerebellar ataxia 25', 'SCA25']",0050974,608703,101111,C1837518,,,,C537202,,,,
mondo:0012104,acquired partial lipodystrophy,"['lipodystophy partial progressive', 'lipodystrophy, cephalothoracic type', 'lipodystrophy, partial, progressive', 'acquired partial lipodystrophy', 'progressive cephalothoracic lipodystrophy', 'lipodystrophy, partial, acquired, susceptibility to', 'lipodystrophy partial acquired', 'lipodystrophy cephalothoracic type', 'Barraquer-Simons syndrome', 'APLD, susceptibility to', 'partial acquired lipodystrophy', 'APLD', 'susceptibility to partial acquired lipodystrophy']",,,79087,C0220989,"['-0.02835', '0.06555', '0.02898', '-0.01212', '0.02304', '-0.1088', '0.03708', '0.0844', '-0.03665', '-0.02606', '-0.03946', '-0.03033', '0.01611', '-0.010956', '-0.05542', '-0.03912', '0.03418', '-0.0357', '-0.01874', '-0.184', '-0.03027', '-0.0665', '0.0807', '-0.01973', '0.02838', '0.000599', '-0.03162', '0.00113', '-0.02129', '-0.0746', '0.112', '-0.03488', '0.10736', '0.06305', '-0.000676', '-0.01331', '-0.005966', '-0.01982', '-0.03262', '-0.07306', '0.0007963', '-0.09106', '0.009224', '0.01952', '0.03986', '-0.0991', '-0.02214', '0.03192', '0.0269', '0.019', '-0.02112', '-0.01729', '0.05118', '0.00842', '-0.087', '-0.02562', '0.08026', '-0.07227', '-0.135', '-0.02528', '0.02438', '0.04504', '0.025', '0.03065', '-0.001205', '0.02551', '0.06125', '0.01326', '-0.0512', '0.103', '-0.0712', '0.008', '0.04703', '-0.08093', '0.04803', '0.03513', '0.06067', '-0.001585', '-0.04922', '-0.0486', '-0.01567', '0.0158', '0.0266', '0.0906', '-0.007122', '0.003138', '0.04666', '0.09894', '0.0838', '0.01956', '0.02225', '0.10834', '-0.01784', '0.02428', '0.1827', '0.01316', '0.1095', '-0.1432', '-0.00171', '0.01884']",C129723,,C562448,,,,
mondo:0012105,granulomatosis with polyangiitis,"['Wegener granulomatosis', 'necrotizing respiratory granulomatosis', 'granulomatosis with polyangiitis', 'pauci-immune glomerulonephritis associated with granulomatosis with polyangiitis', 'Midline granulomatosis', 'GPA', 'Wegener^s syndrome', 'granulomatosis - Wegener^s', 'Wg', 'Wegener^s granulomatosis', 'ANCA-associated vasculitis']",12132,608710,900,C4050407,,C3444,0005297,D014890,446.4,M31.3,10047888,
mondo:0012106,"microcephaly 5, primary, autosomal recessive","['microcephaly 5, primary, autosomal recessive', 'MCPH5', 'ASPM autosomal recessive primary microcephaly', 'autosomal recessive primary microcephaly caused by mutation in ASPM']",0070280,608716,,C1837501,,,,C563871,,,,
mondo:0012107,"neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia","['neuropathy, hereditary sensory and autonomic, adult-onset, with anosmia']",,608720,,C1837492,,,,C563870,,,,
mondo:0012108,"spondyloepimetaphyseal dysplasia, matrilin-3 type","['SEMD, MATN3-related', 'spondyloepimetaphyseal dysplasia matrilin-3 type', 'spondyloepimetaphyseal dysplasia, matrilin-3 related', 'SEMD MATN3-related', 'spondyloepimetaphyseal dysplasia matrilin-3 related', 'SEMD, matrilin-3 type', 'spondyloepimetaphyseal dysplasia, Borochowitz-Cormier-Daire type']",,608728,156728,C1837481,"['-0.8374', '0.376', '0.245', '-0.3887', '0.4612', '-0.583', '-0.3313', '0.7607', '-0.5776', '-0.3171', '0.02153', '-0.0735', '-0.0658', '0.0084', '0.2542', '0.2468', '0.3494', '0.302', '-0.517', '-0.337', '-0.1046', '-0.2113', '0.532', '-0.219', '0.05878', '0.0972', '-0.06537', '0.1162', '0.4312', '-0.2382', '0.4119', '-0.62', '-0.1141', '-0.0723', '0.4495', '-0.4937', '-0.39', '-0.6226', '0.2546', '-0.551', '-0.2422', '-0.5713', '-0.08905', '-0.1877', '-0.3535', '-0.3086', '-0.1843', '0.273', '0.1904', '-0.4353', '0.1562', '0.05664', '-0.11', '0.1704', '-0.0594', '-1.075', '-0.1583', '-0.2742', '0.0334', '0.202', '0.4402', '-0.1196', '-0.3599', '0.1617', '-0.4023', '0.0591', '0.0339', '0.3086', '-0.3896', '0.264', '-0.598', '0.1437', '0.1525', '-0.06216', '-0.4885', '0.777', '-0.45', '0.486', '-0.1407', '-0.2583', '-0.1351', '0.1666', '-0.0466', '0.441', '0.02242', '0.2568', '-0.0959', '0.526', '0.2213', '0.08405', '-0.608', '0.0532', '-0.0699', '0.1506', '0.669', '0.2065', '0.524', '-0.8667', '0.05072', '0.0766']",,,C563869,,,,
mondo:0012109,"hypertension, essential, susceptibility to, 4","['hypertension, essential, susceptibility to, 4', 'Hyt4', 'hypertension, essential, susceptibility to, type 4']",,608742,,C1837479,,,,,,,,
mondo:0012110,growth delay due to insulin-like growth factor type 1 deficiency,"['IGF1 deficiency', 'growth retardation with deafness and mental retardation due to IGF1 deficiency', 'insulin-like growth Factor 1 deficiency', 'growth retardation with sensorineural deafness and intellectual disability', 'IGF-1 deficiency', 'insulin-like growth factor I deficiency', 'growth retardation with sensorineural deafness and mental retardation', 'growth delay-deafness- intellectual disability syndrome', 'primary insulin-like growth factor deficiency']",,608747,73272,C4518327,"['-0.2874', '0.1442', '0.1833', '-0.2844', '0.3157', '0.1134', '0.2522', '0.816', '-0.147', '-0.8726', '-0.408', '-0.3228', '0.2062', '0.0298', '0.04852', '-0.03763', '0.597', '0.015366', '-0.6675', '-0.99', '0.3125', '-0.4392', '0.1186', '-0.1805', '0.10675', '0.572', '-0.2429', '-0.3708', '0.5137', '-0.5537', '0.4731', '0.3599', '0.4685', '0.2773', '-0.9165', '-0.3496', '0.0632', '-0.4197', '-0.32', '0.0862', '0.4465', '-0.1425', '0.1951', '0.1996', '0.05637', '-0.1785', '0.0875', '-0.5405', '-0.459', '-0.02988', '-0.0517', '-0.598', '0.1462', '0.621', '-0.613', '0.4456', '0.11676', '-0.4998', '-0.4768', '0.8335', '-0.08765', '-0.12305', '0.2152', '-0.1539', '-0.2236', '0.2035', '-0.3157', '0.4426', '-0.504', '0.4006', '-0.284', '0.346', '-0.1648', '-0.4321', '0.766', '-0.2279', '0.0177', '-0.1891', '0.2123', '0.2195', '-0.1356', '0.5356', '-0.2808', '0.4404', '-0.2339', '0.2396', '0.339', '0.7275', '0.4429', '0.4727', '0.524', '0.6265', '-0.337', '-0.2222', '0.6577', '0.1808', '-0.2454', '-0.744', '0.3352', '0.0455']",,,C563867,,,,
mondo:0012111,hypertrophic cardiomyopathy 8,"['cardiomyopathy, familial hypertrophic, type 8', 'hypertrophic cardiomyopathy type 8', 'cardiomyopathy, familial hypertrophic, 8', 'MYL3 hypertrophic cardiomyopathy', 'CMH8', 'hypertrophic cardiomyopathy caused by mutation in MYL3', 'cardiomyopathy hypertrophic mid-left ventricular chamber type 1', 'cardiomyopathy, hypertrophic, 8', 'cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 1']",0110314,608751,,C1837471,,,,C563866,,,,
mondo:0012112,hypertrophic cardiomyopathy 10,"['CMH10', 'hypertrophic cardiomyopathy caused by mutation in MYL2', 'MYL2 hypertrophic cardiomyopathy', 'hypertrophic cardiomyopathy type 10', 'cardiomyopathy, hypertrophic, mid-left ventricular chamber type, 2', 'cardiomyopathy, hypertrophic, 10', 'cardiomyopathy, familial hypertrophic, 10', 'cardiomyopathy, familial hypertrophic, type 10']",0110316,608758,,C1834460,,,,C563865,,,,
mondo:0012113,"epilepsy, idiopathic generalized, susceptibility to, 3","['epilepsy, idiopathic generalized, susceptibility to, locus on chromosome 9', 'epilepsy, idiopathic generalized, susceptibility to, 3', 'EIG3']",0111318,608762,,,,,,,,,,
mondo:0012114,"Ehlers-Danlos syndrome, Beasley-Cohen type","['Ehlers-Danlos syndrome with mental retardation, deafness, and cataract', 'Ehlers-Danlos syndrome with intellectual disability, deafness, and cataract', 'Ehlers-Danlos syndrome, Beasley-Cohen type']",,608763,,C1837462,,,,C536199,,,,
mondo:0012115,"scoliosis, isolated, susceptibility to, 3","['scoliosis, isolated, susceptibility to, 3', 'IS3']",,608765,,,,,,,,,,
mondo:0012116,spinocerebellar ataxia type 8,"['spinocerebellar ataxia 8', 'spinocerebellar ataxia type 8', 'SCA8']",0050959,608768,98760,C4275024,"['-0.07416', '-0.11523', '-0.03174', '0.2051', '-0.1886', '-0.896', '0.0938', '0.1348', '-0.598', '-0.935', '0.10657', '0.2336', '-0.02232', '0.2983', '0.599', '-0.4053', '-0.1594', '-0.2683', '0.01079', '-0.7803', '-0.184', '-0.3835', '0.4285', '-0.7427', '0.548', '-0.3687', '-0.429', '0.279', '-0.301', '-0.9106', '0.3035', '0.603', '-0.57', '-0.2917', '0.446', '0.07166', '-0.325', '0.0359', '0.469', '0.5864', '0.2467', '0.2336', '-0.4307', '0.4512', '0.5806', '-0.522', '0.1831', '0.4514', '0.3127', '0.08075', '-0.225', '0.1769', '-0.0329', '-0.4958', '-0.02135', '-0.8335', '0.3633', '0.5127', '-0.144', '0.3782', '-0.4983', '0.2334', '0.446', '-0.0974', '-0.4734', '0.5415', '0.1732', '0.5728', '-0.6016', '0.5938', '0.6035', '0.4766', '-0.0907', '-0.6797', '0.6587', '0.4326', '0.2423', '0.2119', '0.1265', '0.6216', '-0.2483', '-0.9834', '0.4502', '0.6523', '-0.08215', '-0.653', '0.1182', '0.02887', '0.6367', '0.4111', '0.427', '0.522', '0.0547', '0.09314', '1.064', '1.006', '0.3567', '0.4832', '-0.3435', '-0.063']",,,,,,,
mondo:0012117,ALG9-congenital disorder of glycosylation,"['CDG syndrome type IL', 'CDG1L', 'carbohydrate deficient glycoprotein syndrome type 1L', 'congenital disorder of glycosylation, type IL', 'congenital disorder of glycosylation type IL', 'mannosyltransferase 7-9 deficiency', 'ALG9-CDG', 'CDG-IL', 'CDG 1L', 'congenital disorder of glycosylation type 1L', 'carbohydrate deficient glycoprotein syndrome type IL', 'CDG IL', 'ALG9-CDG (CDG-IL)']",0080564,608776,79328,C2931006,"['-0.2404', '0.3179', '0.2499', '-0.463', '0.1348', '-0.494', '-0.1296', '0.2087', '-0.7', '-0.04782', '-0.2908', '-0.3882', '0.1293', '-0.3665', '-0.3762', '0.0457', '-0.00843', '-0.2998', '-0.2805', '-0.7656', '0.602', '0.01512', '0.01221', '-0.3022', '0.1669', '-0.2074', '-0.2144', '0.001312', '0.4111', '-0.3384', '0.2393', '0.1555', '0.715', '0.2368', '0.2251', '-0.0937', '-0.511', '-0.0007997', '-0.2864', '-0.1729', '-0.2424', '-0.1061', '0.2688', '0.2114', '-0.44', '-0.1461', '0.01261', '0.1162', '0.1592', '0.1915', '-0.1367', '0.11456', '-0.0488', '0.3708', '-0.1426', '-0.4717', '0.01119', '0.1152', '-0.1797', '0.656', '0.4324', '-0.1054', '-0.2108', '-0.00894', '0.1526', '-0.3125', '0.374', '0.2546', '-0.2637', '0.3992', '-0.2048', '0.2654', '0.4778', '0.2908', '-0.334', '0.2534', '0.5957', '-0.2216', '-0.3303', '0.3232', '0.1476', '0.1127', '-0.3506', '0.1436', '-0.1937', '0.0943', '0.1064', '0.5854', '0.2056', '0.3718', '-0.0839', '0.2798', '0.1316', '-0.03986', '0.4607', '0.5073', '0.864', '-0.0239', '0.3303', '0.1213']",,,C535750,,,,
mondo:0012118,COG7-congenital disorder of glycosylation,"['CDG2E', 'CDG 2E', 'CDG IIe', 'congenital disorder of glycosylation type 2e', 'congenital disorder of glycosylation, type IIe', 'CDG syndrome type IIe', 'carbohydrate deficient glycoprotein syndrome type IIe', 'CDG-IIe', 'COG7-CDG', 'congenital disorder of glycosylation type IIe', 'COG7-CDG (CDG-IIe)']",,608779,79333,,"['-0.1965', '0.4912', '0.0705', '-0.00745', '0.259', '-0.915', '0.1431', '0.632', '-0.2109', '-0.371', '-0.321', '-0.0334', '0.2505', '0.03445', '-0.0715', '0.0696', '-0.03168', '0.004894', '-0.607', '-0.3943', '0.1901', '-0.0163', '0.3694', '-0.1448', '0.4111', '-0.10095', '-0.10364', '0.4282', '0.08673', '-0.2925', '0.3313', '0.01761', '0.205', '-0.01585', '-0.05698', '0.2148', '-0.0991', '-0.363', '-0.6753', '0.1053', '-0.05307', '-0.2559', '0.08704', '-0.09906', '-0.2888', '0.12164', '-0.172', '-0.0758', '-0.2817', '-0.0927', '-0.309', '-0.03723', '0.02763', '0.3003', '0.1649', '-0.5054', '0.3992', '0.2778', '0.02904', '0.5347', '0.2499', '-0.01614', '0.2302', '0.03622', '0.154', '-0.2847', '0.4453', '0.0229', '-0.583', '-0.013985', '0.0766', '-0.0671', '0.2301', '0.09717', '-0.11115', '0.0811', '0.3662', '0.4377', '-0.1978', '0.3882', '0.2452', '0.3745', '0.003574', '-0.012146', '-0.0015335', '-0.02074', '0.367', '0.7183', '0.598', '-0.1974', '-0.2184', '0.532', '0.23', '-0.3215', '0.625', '0.5303', '0.3943', '-0.786', '0.415', '-0.2433']",,,C535754,,,,
mondo:0012119,"asperger syndrome, susceptibility to, 3","['Asperger syndrome susceptibility 3', 'ASPG3', 'ASPERGER syndrome, susceptibility to, 3']",,608781,,C1837434,,,,,,,,
mondo:0012120,pyruvate dehydrogenase phosphatase deficiency,"['PDH phosphatase deficiency', 'PDHPD', 'lactic acidemia with pyruvate dehydrogenase phosphatase deficiency', 'pyruvate dehydrogenase phosphatase deficiency']",,608782,79246,C1837429,"['-0.2925', '0.3533', '-0.4783', '0.6074', '0.1418', '-0.5107', '-0.2434', '0.824', '-0.0186', '-0.03632', '-0.2274', '-0.00188', '0.0546', '-0.01166', '0.015366', '0.1254', '-0.10284', '-0.4177', '-0.278', '-0.608', '-0.338', '-0.002153', '0.687', '-0.04822', '0.3076', '0.137', '-0.2732', '0.03696', '0.000933', '-0.3867', '0.3003', '0.0957', '0.2625', '0.396', '-0.1881', '-0.07983', '-0.2927', '-0.3828', '-0.2983', '0.1674', '0.2441', '-0.532', '0.1948', '-0.05728', '-0.1538', '0.1268', '-0.2644', '0.2051', '-0.1692', '0.2893', '-0.0855', '-0.526', '-0.1821', '0.0211', '-0.3057', '-0.468', '0.3206', '-0.2876', '-0.04788', '0.4658', '0.3179', '-0.2316', '0.5215', '-0.19', '-0.0667', '0.1665', '0.4146', '0.0952', '-0.5903', '0.2588', '0.3896', '0.2013', '-0.06366', '0.1571', '0.4126', '0.5073', '-0.0186', '-0.4697', '-0.1242', '0.1425', '-0.0408', '0.02367', '-0.3672', '-0.185', '0.6724', '0.241', '0.1021', '0.01285', '1.097', '-0.1147', '0.3623', '0.4585', '-0.1769', '-0.05255', '0.4707', '0.2352', '-0.001535', '-0.2637', '0.1372', '-0.1327']",,,C536258,,,,
mondo:0012121,otosclerosis 5,"['OTSC5', 'otosclerosis 5']",,608787,,C1837422,,,,C563858,,,,
mondo:0012122,moyamoya disease 3,"['Moyamoya disease 3', 'MYMY3']",,608796,,C1837418,,,,C536993,,,,
mondo:0012123,congenital disorder of glycosylation type 1E,"['CDGIe', 'CDG Ie', 'congenital disorder of glycosylation caused by mutation in DPM1', 'congenital disorder of glycosylation type 1e', 'CDG syndrome type Ie', 'carbohydrate deficient glycoprotein syndrome type Ie', 'DPM1 congenital disorder of glycosylation', 'congenital disorder of glycosylation type Ie', 'carbohydrate-deficient glycoprotein syndrome type 1E', 'CDG1E', 'Dol-P-mannosyltransferase deficiency', 'CDG 1E', 'CDG-Ie', 'DPM1-CDG', 'congenital disorder of glycosylation, type Ie', 'DPM1-CDG (CDG-Ie)']",0080557,608799,79322,,"['-0.3438', '0.1855', '0.195', '-0.1561', '0.1646', '-0.261', '-0.0641', '0.55', '-0.23', '-0.1827', '-0.1663', '-0.255', '0.10693', '-0.1769', '-0.02663', '0.2656', '0.2998', '-0.02899', '-0.4673', '-0.5464', '0.2295', '0.00916', '0.2905', '-0.2457', '0.1324', '0.003614', '-0.5103', '-0.4114', '0.2578', '-0.0782', '0.3813', '0.265', '0.1578', '0.2986', '-0.2185', '0.17', '0.02701', '-0.3057', '-0.5796', '-0.0481', '0.1833', '-0.5166', '-0.1572', '0.04245', '-0.1804', '-0.3506', '0.2338', '0.2225', '0.2386', '0.0401', '-0.2642', '-0.00908', '-0.04166', '0.1882', '-0.03093', '-0.653', '0.2988', '0.1606', '-0.05612', '0.658', '0.116', '0.0835', '0.4856', '0.24', '-0.0846', '-0.3955', '-0.1989', '0.10706', '-0.7793', '0.1599', '-0.628', '0.2712', '-0.0669', '0.3416', '0.1367', '0.3054', '0.07336', '-0.2228', '-0.2001', '0.1868', '0.2391', '0.2054', '-0.1678', '0.544', '-0.01194', '-0.1157', '0.2688', '0.746', '0.3271', '0.2463', '0.2288', '0.6904', '0.0767', '-0.3389', '0.4326', '0.6777', '0.3916', '-0.4', '0.2327', '0.06183']",C126871,,C535743,,,,
mondo:0012124,sudden infant death-dysgenesis of the testes syndrome,"['SIDDT', 'sudden infant death - dysgenesis of the testes', 'sudden infant death with dysgenesis of the testes syndrome']",,608800,168593,C1837371,"['0.118', '0.5435', '-0.311', '0.1162', '-0.2108', '-0.3818', '-0.1132', '0.8423', '0.04022', '-0.3242', '-0.2837', '-0.4424', '-0.409', '0.1815', '0.3083', '0.1652', '0.0679', '0.1051', '-0.2133', '-0.7256', '-0.2194', '0.02463', '-0.01', '-0.4656', '0.659', '-0.591', '-0.1246', '0.4521', '0.2598', '-0.2927', '0.5874', '-0.07983', '0.4365', '0.0619', '-0.2421', '0.2327', '0.1327', '-0.511', '-0.09357', '0.03772', '0.5435', '-0.08655', '-0.1809', '-0.07007', '-0.1807', '-0.1251', '-0.2805', '0.1604', '-0.06805', '0.5234', '-0.1577', '-0.1493', '-0.5913', '-0.0694', '0.1392', '0.03174', '0.322', '-0.03494', '0.2988', '0.574', '0.338', '0.167', '0.02328', '0.6245', '-0.4065', '0.004288', '0.8022', '0.3909', '-0.571', '0.385', '-0.2015', '0.739', '0.2852', '-0.0591', '-0.306', '-0.4526', '-0.0526', '0.18', '-0.717', '-0.10693', '0.09015', '0.531', '0.01828', '-0.277', '-0.05582', '0.04608', '0.0946', '-0.0495', '0.1421', '-0.22', '-0.1333', '0.4426', '-0.03632', '0.4053', '0.4988', '0.1893', '0.0674', '-0.2788', '0.2231', '0.0697']",,,C563856,,,,
mondo:0012125,hypomyelinating leukodystrophy 2,"['PMLD1', 'Pelizaeus-Merzbacher-like disease 1', 'GJC2 leukodystrophy', 'Pelizaeus-Merzbacher-like disease due to GJC2 mutation', 'hypomyelinating leukodystrophy type 2', 'Pelizaeus-Merzbacher-like disease, 1', 'leukodystrophy caused by mutation in GJC2', 'leukodystrophy, hypomyelinating, 2', 'HLD2', 'leukodystrophy, hypomyelinating, type 2']",0060787,608804,280282,C1837355,"['-0.301', '0.2292', '0.02257', '0.0412', '0.1042', '-0.291', '-0.1186', '0.1516', '-0.2666', '-0.10065', '-0.06836', '0.02765', '-0.09064', '-0.0883', '0.2074', '-0.1843', '-0.0686', '-0.1037', '-0.1285', '-0.267', '0.1434', '-0.1373', '0.1028', '0.00676', '0.148', '-0.013', '-0.0021', '0.0739', '0.01846', '-0.01339', '0.0725', '0.1018', '0.1837', '0.0233', '0.1698', '-0.147', '0.03873', '-0.0454', '0.10895', '-0.2212', '0.0842', '-0.1677', '0.11316', '0.03928', '-0.1361', '-0.2385', '0.03137', '0.0763', '0.1843', '-0.007904', '0.0628', '-0.0671', '-0.03207', '0.01735', '-0.142', '-0.182', '0.3533', '0.0246', '-0.2678', '0.1416', '0.06287', '0.1495', '0.2062', '-0.003328', '0.1242', '0.1665', '0.1804', '0.05878', '-0.1592', '0.11005', '-0.278', '0.01138', '0.06854', '-0.1687', '0.12317', '0.04868', '0.07526', '0.1131', '-0.1663', '-0.005077', '-0.0367', '-0.063', '-0.047', '0.1145', '-0.02606', '-0.1902', '0.1855', '0.273', '0.2283', '0.1512', '0.07007', '0.0216', '-0.01782', '-0.0858', '0.4426', '0.1719', '0.217', '-0.337', '-0.01576', '-0.03488']",,,C563855,,,,
mondo:0012126,familial avascular necrosis of femoral head,"['ischaemic Necrosis of femoral head', 'osteonecrosis of femoral head', 'primary avascular necrosis of the femoral head', 'familial avascular necrosis of the femoral head', 'aseptic Necrosis of head of femur', 'avascular NECROSIS of femoral head, primary', 'femoral head, avascular Necrosis of', 'femoral head, aseptic Necrosis of', 'avascular NECROSIS of femoral head, primary, 1', 'aseptic Necrosis of femoral head', 'ANFH1', 'ischemic Necrosis of femoral head', 'avascular Necrosis of femoral head, primary, 1', 'familial osteonecrosis of the femoral head', 'ANFH']",,,86820,CN206226,,C35480,,D005271,,,,
mondo:0012127,autosomal recessive limb-girdle muscular dystrophy type 2J,"['LGMD2J', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in TTN', 'limb-girdle muscular dystrophy type 2J', 'TTN autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, limb-girdle, autosomal recessive 10', 'muscular dystrophy, limb-girdle, type 2J']",0110283,608807,140922,C1837342,,,,C563854,,,,
mondo:0012128,"transposition of the great arteries, dextro-looped","['D-TGA', 'dextro-looped transposition of the great arteries caused by mutation in MED13L', 'DTGA1', 'DTGA', 'dextro-looped transposition of the great arteries type 1', 'transposition of the great arteries, dextro-looped 1', 'MED13L dextro-looped transposition of the great arteries', 'transposition of the great arteries, dextro-looped type 1', 'dextro-looped transposition of the great arteries 1']",0060771,608808,,C1837341,,,,C563853,,,,
mondo:0012129,"leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema","['LACH', 'leukoencephalopathy, arthritis, colitis, and hypogammaglobulinema']",,608809,,C1837329,,,,C563852,,,,
mondo:0012130,myofibrillar myopathy 2,"['myopathy, desmin-related, associated with mutation in the Cryab Gene', 'MFM2', 'myopathy, myofibrillar, 2', 'CRYAB autosomal dominant distal myopathy', 'myopathy, myofibrillar, alpha-B crystallin-related', 'alpha-B crystallinopathy', 'autosomal dominant distal myopathy caused by mutation in CRYAB', 'myopathy, myofibrillar, type 2', 'late-onset distal crystallinopathy', 'alpha-B crystallin-related late-onset distal myopathy', 'myopathy, myofibrillar, with or without cataract and/or cardiomyopathy', 'myofibrillar myopathy type 2']",0080093,608810,399058,C1837317,"['-0.498', '0.00878', '-0.08203', '-0.2424', '-0.0603', '-0.574', '0.1769', '0.516', '-0.7324', '-0.2384', '-0.3203', '-0.1398', '-0.3198', '0.0845', '0.1702', '0.03815', '-0.3052', '-0.1476', '-0.2465', '-0.4849', '0.6616', '-0.1528', '0.147', '0.516', '0.1771', '0.072', '0.2029', '-0.1306', '-0.1837', '-0.01485', '0.3335', '0.298', '0.2717', '0.06024', '0.3125', '-0.0648', '-0.2239', '-0.1438', '0.01465', '-0.343', '0.02586', '-0.54', '0.04388', '0.628', '-0.001732', '-0.51', '-0.2854', '0.2837', '0.221', '0.3792', '0.0511', '0.00436', '0.05826', '-0.374', '-0.09503', '-0.869', '0.619', '0.10504', '0.0786', '-0.1431', '0.3562', '-0.04825', '-0.01953', '-0.258', '-0.641', '0.03607', '0.3433', '0.6436', '-0.1636', '0.2732', '-0.139', '-0.333', '0.3022', '0.03732', '0.2578', '-0.338', '-0.06903', '0.08954', '-0.2367', '-0.1324', '0.335', '0.1102', '0.5522', '0.1626', '-0.2163', '0.03812', '-0.04156', '0.22', '0.2368', '-0.2864', '0.4912', '-0.1876', '0.261', '0.269', '0.6416', '0.1635', '0.6294', '0.0109', '-0.269', '-0.0805']",,,C563848,,,,
mondo:0004046,childhood brain meningioma,"['childhood meningioma of brain', 'paediatric brain meningioma', 'paediatric meningioma of the brain', 'pediatric meningioma of brain', 'brain pediatric meningioma', 'paediatric meningioma of brain', 'pediatric meningioma of the brain', 'childhood meningioma of the brain', 'pediatric brain meningioma', 'brain paediatric meningioma', 'Brain meningioma']",6939,,,C1332949,,C6253,,,,,,
mondo:0004047,sphenoidal sinus neoplasm,"['tumour of the sphenoidal sinus', 'sphenoidal sinus tumour', 'neoplasm of the sphenoidal sinus', 'sphenoidal sinus tumor', 'tumor of sphenoid sinus', 'tumour of sphenoidal sinus', 'tumor of the sphenoid sinus', 'neoplasm of sphenoidal sinus', 'sphenoidal sinus neoplasm (disease)', 'neoplasm of the sphenoid sinus', 'sphenoid sinus neoplasm', 'tumor of sphenoidal sinus', 'sphenoid sinus tumour', 'tumour of the sphenoid sinus', 'tumour of sphenoid sinus', 'tumor of the sphenoidal sinus', 'sphenoidal sinus neoplasm', 'sphenoid sinus tumor', 'neoplasm of sphenoid sinus']",6947,,,C0345676,,C6792,,,,,,
mondo:0004048,immature gastric teratoma,"['malignant teratoma of the stomach', 'stomach malignant teratoma', 'malignant gastric teratoma', 'malignant teratoma of stomach', 'immature gastric teratoma']",6948,,,C1334151,,C5256,,,,,,
mondo:0004049,combat disorder,"['stress disorders, combat', 'combat neurosis', 'neuroses, war', 'disorders, combat stress', 'war neurosis', 'Shocks, shell', 'combat disorder', 'disorders, combat', 'neurosis, combat', 'disorder, combat stress', 'shell Shocks', 'combat neuroses', 'stress disorder, combat', 'war neuroses', 'disorder, combat', 'neuroses, combat', 'combat stress disorders', 'combat stress disorder', 'shock, shell', 'neurosis, war', 'shell shock']",6950,,,,,,,D003130,,,,
mondo:0004050,telangiectatic osteogenic sarcoma,"['malignant bone aneurysm', 'TEOS', 'telangiectatic osteosarcoma (morphologic abnormality)', 'telangiectatic osteosarcoma']",6951,,,C0259782,,C3902,,,,,,
mondo:0004051,aleukemic monocytic leukemia cutis,['aleukemic monocytic leukemia cutis'],6958,,,C1332232,,C5630,,,,,,
mondo:0004052,rectal cloacogenic carcinoma,"['rectal transitional zone carcinoma', 'transition zone carcinoma of rectum', 'cloacogenic carcinoma of the rectum', 'transitional zone carcinoma of the rectum', 'rectal cloacogenic carcinoma', 'cloacogenic carcinoma of rectum', 'transition zone carcinoma of the rectum', 'rectal transition zone carcinoma', 'transitional zone carcinoma of rectum']",6959,,,C1333074,,C5555,,,,,,
mondo:0004053,bartholin gland squamous cell carcinoma,"['Bartholin^s gland squamous cell carcinoma', 'major vestibular gland squamous cell carcinoma', 'bartholin gland squamous cell carcinoma']",6961,,,C1511052,,C40293,1000104,,,,,
mondo:0004054,acute canaliculitis,"['acute lacrimal canaliculitis', 'acute canaliculitis, lacrimal']",6969,,,C0339130,,,,,375.31,,,
mondo:0004055,acute inflammation of lacrimal passage,,6970,,,C0339129,,,,,375.3,,,
mondo:0004056,bladder papillary urothelial carcinoma,"['bladder urothelial papillary carcinoma', 'urinary bladder papillary transitional cell carcinoma', 'urothelial papillary carcinoma of the bladder', 'bladder papillary urothelial carcinoma']",6975,,,C1518882,,C7383,,,,,,
mondo:0004057,micropapillary variant infiltrating bladder urothelial carcinoma,"['infiltrating bladder urothelial carcinoma, micropapillary variant']",6976,,,C1517579,,C27202,0008512,,,,,
mondo:0004058,pancreatic cholera,"['WDHH', 'excessive vasoactive intestinal peptide secretion', 'WDHA syndrome', 'pancreatic WDHA syndrome', 'watery diarrhea, hypokalemia, and achlorhydria syndrome', 'watery diarrhoea with hypokalemic alkalosis', 'Verner Morrison syndrome', 'islet cell WDHA syndrome', 'watery diarrhea with hypokalemic alkalosis', 'watery diarrhoea syndrome', 'watery diarrhea syndrome']",6977,,,,,C3488,,D003969,259.3,,,
mondo:0004059,dentin sensitivity,['sensitive dentin'],698,,,C0011432,,,,D003807,,,,
mondo:0004060,peripheral epithelioid sarcoma,"['distal-type epithelioid sarcoma', 'conventional epithelioid sarcoma']",6988,,,C1333306,,C27473,,,,,,
mondo:0004062,intermediate cell type uveal melanoma,"['intraocular mixed cell type melanoma', 'Intermediate cell type uveal melanoma', 'Intermediate cell type intraocular melanoma', 'mixed cell type uveal melanoma']",6992,,,C0279693,,C7989,,,,,,
mondo:0004063,intermediate cell type iris melanoma,"['intermediate cell type uveal melanoma of iris', 'Intermediate cell type iris melanoma', 'iris intermediate cell type uveal melanoma', 'iris mixed cell melanoma']",6993,,,C1334210,,C6101,,,,,,
mondo:0004064,iris melanoma,"['malignant melanoma of the iris', 'melanoma of iris', 'iris melanoma', 'malignant iris melanoma', 'iris melanoma (disease)', 'malignant melanoma of iris', 'iris malignant melanoma', 'melanoma of the iris']",6994,,,CN204945,,C9088,,,,,,
mondo:0004065,intermediate cell type choroid melanoma,"['mixed cell melanoma of choroid', 'Intermediate cell type choroid melanoma', 'intermediate cell type uveal melanoma of optic choroid', 'optic choroid intermediate cell type uveal melanoma']",6996,,,C1334208,,C6100,,,,,,
mondo:0004066,intermediate cell type ciliary body melanoma,"['ciliary body intermediate cell type uveal melanoma', 'Intermediate cell type ciliary body melanoma', 'intermediate cell type uveal melanoma of ciliary body']",6997,,,C1334209,,C6118,,,,,,
mondo:0004067,gallbladder mucinous adenocarcinoma,"['mucinous carcinoma of the gallbladder', 'gallbladder mucinous carcinoma', 'colloid carcinoma of gallbladder', 'colloidal carcinoma of gallbladder', 'gallbladder mucinous adenocarcinoma', 'gallbladder colloidal carcinoma', 'colloidal carcinoma of the gallbladder', 'mucinous carcinoma of gallbladder', 'gallbladder colloid carcinoma', 'gall bladder mucinous adenocarcinoma', 'colloid carcinoma of the gallbladder']",6998,,,C1333750,,C5744,,,,,,
mondo:0004069,inborn mitochondrial metabolism disorder,"['mitochondrial genetic disorders', 'mitochondrial metabolism disease', 'mitochondrial disease']",700,,68380,CN552492,,,,D028361,,,,
mondo:0004071,childhood cerebral astrocytoma,"['paediatric astrocytoma of cerebrum', 'telencephalon juvenile astrocytoma', 'paediatric astrocytoma of the cerebrum', 'childhood astrocytic tumour of telencephalon', 'childhood astrocytoma of cerebrum', 'childhood astrocytic tumor of telencephalon', 'pediatric cerebral astrocytoma', 'pediatric astrocytoma of cerebrum', 'telencephalon childhood astrocytic tumor', 'paediatric cerebral astrocytoma', 'telencephalon childhood astrocytic tumour', 'childhood astrocytoma of the cerebrum', 'cerebral astrocytoma, childhood', 'pediatric astrocytoma of the cerebrum', 'cerebral astrocytoma']",7007,,,C0338070,,C4347,,,,,,
mondo:0004074,ovarian mucinous cystadenofibroma,['ovarian mucinous cystadenofibroma'],7013,,,C1518725,,C40041,,,,,,
mondo:0004075,infiltrating lipoma,"['intramuscular lipoma', 'intramuscular lipoma (morphologic abnormality)']",7014,,,C0334473,,C7451,,,,,,
mondo:0004076,tendon sheath lipoma,"['lipoma of the tendon sheath', 'lipoma of tendon sheath', 'tendon sheath lipoma']",7016,,,C1336703,,C6499,,,,,,
mondo:0004077,lumbosacral lipoma,['sacral region of vertebral column lipoma'],7017,,,C1334438,,C6500,,,,,,
mondo:0004078,mucinous intrahepatic cholangiocarcinoma,"['mucin-producing intrahepatic cholangiocarcinoma', 'mucinous intrahepatic cholangiocarcinoma']",7024,,,C1513718,,C41618,,,,,,
mondo:0004079,lung mucous gland adenoma,"['bronchial cystadenoma', 'adenoma of the bronchial mucous gland', 'lung mucous gland adenoma', 'adenoma of the bronchial mucus gland', 'adenoma of bronchial mucous gland', 'adenoma of bronchial mucus gland', 'lung polyadenoma', 'bronchial mucus gland adenoma']",7030,,,C1332640,,C5664,,,,,,
mondo:0004080,glottis squamous cell carcinoma,"['squamous cell carcinoma of the glottis', 'squamous cell carcinoma of glottis', 'epidermoid carcinoma of glottis', 'glottis epidermoid carcinoma', 'glottic squamous cell carcinoma', 'epidermoid carcinoma of the glottis', 'glottic epidermoid carcinoma', 'glottis squamous cell carcinoma']",7031,,,C0280325,,C8186,,,,,,
mondo:0004081,extrahepatic bile duct clear cell adenocarcinoma,"['extrahepatic bile duct clear cell adenocarcinoma', 'bile duct clear cell adenocarcinoma', 'clear cell adenocarcinoma of bile duct', 'bile duct clear cell carcinoma', 'clear cell adenocarcinoma of the bile duct', 'clear cell bile duct adenocarcinoma']",7032,,,C0861855,,C5775,,,,,,
mondo:0004082,childhood immature teratoma of ovary,"['pediatric immature teratoma of the ovary', 'childhood ovarian immature teratoma', 'childhood immature teratoma of the ovary', 'paediatric immature teratoma of ovary', 'paediatric ovarian immature teratoma', 'paediatric immature teratoma of the ovary', 'immature ovarian teratoma of childhood', 'pediatric ovarian immature teratoma', 'paediatric immature ovarian teratoma', 'childhood immature ovarian teratoma', 'pediatric immature ovarian teratoma', 'pediatric immature teratoma of ovary']",7037,,,C1332990,,C6547,,,,,,
mondo:0004083,Borst-Jadassohn intraepidermal carcinoma,"['Bowen^s disease, clonal', 'intraepidermal epithelioma of Jadassohn']",7039,,,C2937231,,C4110,1001841,,,,,
mondo:0004085,choroid epithelioid cell melanoma,"['epithelioid cell melanoma of choroid', 'epithelioid cell melanoma of optic choroid', 'choroid epithelioid cell melanoma', 'choroidal epithelioid cell melanoma', 'optic choroid epithelioid cell melanoma', 'epithelioid cell melanoma of the choroid']",7041,,,C1333024,,C6102,,,,,,
mondo:0004086,ciliary body epithelioid cell melanoma,"['epithelioid cell melanoma of the ciliary body', 'ciliary body epithelioid cell melanoma', 'epithelioid cell melanoma of ciliary body']",7042,,,C1333050,,C6119,,,,,,
mondo:0004087,basaloid large cell lung carcinoma,"['basaloid large cell lung carcinoma', 'basaloid large cell carcinoma of the lung', 'basaloid lung carcinoma']",7045,,,C1332463,,C7266,,,,,,
mondo:0004088,cervical basaloid carcinoma,"['cervical basaloid carcinoma', 'cervical basaloid squamous cell carcinoma']",7046,,,C1511063,,C40189,,,,,,
mondo:0004089,basaloid carcinoma of the penis,"['basaloid squamous cell carcinoma of the penis', 'basaloid carcinoma of the penis', 'squamous cell carcinoma of the penis, basaloid type', 'basaloid squamous cell carcinoma of penis', 'penis basaloid squamous cell carcinoma', 'basaloid carcinoma of penis', 'penis basaloid carcinoma', 'squamous cell carcinoma of penis, basaloid type', 'BPSCC', 'basaloid penile squamous cell carcinoma']",7047,,,C1332462,,C6980,,,,,,
mondo:0004090,vulvar basaloid squamous cell carcinoma,"['vulvar basaloid carcinoma', 'vulvar basaloid squamous cell carcinoma']",7048,,,C2211850,,C40286,,,,,,
mondo:0004091,skin basaloid carcinoma,"['basaloid squamous cell skin carcinoma', 'zone of skin basaloid squamous cell carcinoma', 'skin basaloid carcinoma', 'skin basaloid squamous cell carcinoma', 'basaloid skin squamous cell carcinoma']",7049,,,C1335973,,C27543,,,,,,
mondo:0004092,thymic basaloid carcinoma,"['basaloid carcinoma of Thymus', 'thymic basaloid carcinoma', 'basaloid carcinoma of the Thymus', 'Thymus basaloid carcinoma', 'thymus basaloid squamous cell carcinoma']",7050,,,C1332464,,C6456,,,,,,
mondo:0004093,esophageal basaloid carcinoma,"['basaloid squamous carcinoma of the esophagus', 'esophageal basaloid cancer', 'basaloid squamous carcinoma of the oesophagus', 'basaloid squamous carcinoma of oesophagus', 'basaloid squamous carcinoma of esophagus', 'esophageal basaloid carcinoma', 'esophageal basaloid squamous cell carcinoma']",7051,,,C1333443,,C7032,,,,,,
mondo:0004094,multiple skull base meningioma,['multiple skull base meningiomas'],7054,,,C1334829,,C5279,,,,,,
mondo:0004095,B-cell neoplasm,"['B-cell neoplasm', 'B-cell lymphocytic neoplasm', 'B-cell lymphoma', 'lymphoma, B-cell']",707,,,,,C27907,,D016393,,,,
mondo:0004096,spinal cord dermoid cyst,"['dermoid cyst of spinal cord', 'dermoid cyst of the spinal cord', 'spinal cord dermoid cyst', 'spinal cord dermoid']",7071,,,C1333278,,C6808,,,,,,
mondo:0004098,malignant melanocytic peripheral nerve sheath tumor of mediastinum,"['mediastinum malignant melanocytic neoplasm of the peripheral nerve sheath', 'malignant mediastinal melanocytic peripheral nerve sheath tumour', 'malignant melanotic peripheral nerve sheath tumor of the mediastinum', 'mediastinal melanocytic MPNST', 'malignant melanocytic neoplasm of the peripheral nerve sheath of mediastinum', 'malignant mediastinal melanocytic peripheral nerve sheath tumor', 'malignant melanocytic peripheral nerve sheath tumor of mediastinum', 'malignant melanotic peripheral nerve sheath tumour of the mediastinum']",7077,,,C1334600,,C6630,,,,,,
mondo:0004099,adult cystic teratoma,"['adult cystic teratoma', 'cystic teratoma of adults']",7079,,,C1368888,,C9012,,,,,,
mondo:0004100,lung mixed small cell and squamous cell carcinoma,"['small cell and large cell carcinoma of the lung', 'small cell and squamous cell carcinoma of the lung', 'combined small cell and squamous cell lung carcinoma', 'mixed small cell and squamous cell carcinoma of the lung', 'small cell and squamous cell lung carcinoma', 'small cell and squamous cell carcinoma of lung', 'mixed small cell and squamous cell carcinoma of lung']",7081,,,C1334788,,C9423,,,,,,
mondo:0004101,multicentric papillary thyroid carcinoma,"['multicentric thyroid gland papillary carcinoma', 'multicentric papillary thyroid gland carcinoma', 'multicentric papillary thyroid carcinoma']",7086,,,C1334817,,C37304,,,,,,
mondo:0004102,columnar cell variant thyroid gland papillary carcinoma,"['columnar cell variant papillary carcinoma', 'columnar cell variant papillary thyroid gland carcinoma', 'columnar cell variant thyroid gland papillary carcinoma']",7088,,,C1333120,,C35830,,,,,,
mondo:0004103,tall cell variant thyroid gland papillary carcinoma,"['tall cell variant papillary carcinoma', 'tall cell variant thyroid gland papillary carcinoma']",7089,,,C1336695,,C35558,,,,,,
mondo:0004104,splenic manifestation of hairy cell leukemia,"['spleen hairy cell leukemia', 'hairy cell leukaemia of spleen', 'spleen hairy cell leukaemia', 'hairy cell leukemia of spleen', 'splenic manifestation of hairy cell leukemia']",709,,,C1336064,,C7301,,,202.47,,,
mondo:0004105,childhood epithelioid sarcoma,"['pediatric epithelioid sarcoma', 'childhood epithelioid sarcoma', 'epithelioid sarcoma', 'epithelioid sarcoma of childhood', 'paediatric epithelioid sarcoma']",7095,,,C0279989,,C8095,,,,,,
mondo:0004106,"testicular yolk sac tumor, macrocystic pattern","['testicular yolk sac tumor, macrocystic pattern', 'macrocystic pattern testicular yolk sac tumor', 'macrocystic pattern testicular yolk sac tumour']",7097,,,C1515307,,C39924,,,,,,
mondo:0004107,splenic manifestation of leukemia,"['splenic leukemia', 'splenic manifestation of leukemia', 'spleen leukemia (disease)', 'leukaemia (disease) of spleen', 'splenic leukaemia', 'spleen leukaemia (disease)']",710,,,C1336065,,C7296,,,,,,
mondo:0004108,diaphragma sellae meningioma,"['meningioma of the diaphragm sellae', 'meningioma of diaphragm sellae', 'diaphragm sellae meningioma', 'meningioma of Diaphragma sellae', 'meningioma of the Diaphragma sellae', 'diaphragma sellae meningioma (disease)']",7103,,,C1333283,,C5283,,,,,,
mondo:0004109,epiglottis neoplasm,"['tumor of Epiglottis', 'tumour of the Epiglottis', 'epiglottic tumour', 'epiglottis neoplasm (disease)', 'Epiglottis tumor', 'epiglottis tumor', 'neoplasm of Epiglottis', 'tumour of epiglottis', 'tumor of epiglottis', 'tumour of Epiglottis', 'neoplasm of epiglottis', 'epiglottis tumour', 'neoplasm of the Epiglottis', 'tumor of the Epiglottis', 'epiglottic neoplasm', 'Epiglottis tumour', 'epiglottic tumor']",7105,,,C1290353,,C4933,,,,,,
mondo:0004110,refractory hairy cell leukemia,"['hairy cell leukemia, refractory', 'refractory hairy cell leukemia']",711,,,C0279780,,C8030,,,,,,
mondo:0004111,refractory hematologic cancer,"['refractory hematologic malignancy', 'refractory hematologic cancer']",712,,,C1335724,,C27357,,,,,,
mondo:0004112,radiation cystitis,['irradiation cystitis'],7127,,,C0156270,,C123174,,,595.82,N30.4,,
mondo:0004114,urinary bladder small cell neuroendocrine carcinoma,"['urinary bladder small cell carcinoma', 'small cell carcinoma of the urinary bladder', 'small cell neuroendocrine carcinoma of the urinary bladder', 'poorly differentiated neuroendocrine carcinoma of the bladder', 'small cell bladder carcinoma', 'small cell carcinoma of the bladder', 'small cell neuroendocrine carcinoma of urinary bladder', 'small cell bladder cancer', 'SCCB', 'bladder small cell neuroendocrine carcinoma', 'small cell/neuroendocrine carcinoma of urinary bladder', 'bladder small cell neuroendocrine cancer', 'small cell carcinoma of urinary bladder']",7132,,284400,CN202866,,C9461,1000129,,,,,
mondo:0004116,esophageal small cell neuroendocrine carcinoma,"['esophageal small cell carcinoma', 'oesophagus Oat cell carcinoma', 'Oat cell carcinoma of oesophagus', 'Oat cell carcinoma of the oesophagus', 'Oat cell carcinoma of esophagus', 'small cell carcinoma of esophagus', 'esophagus Oat cell carcinoma', 'esophageal Oat cell carcinoma', 'small cell carcinoma of oesophagus', 'oesophagus small cell carcinoma', 'small cell carcinoma of the esophagus', 'small cell carcinoma of the oesophagus', 'esophageal small cell neuroendocrine carcinoma', 'esophageal small cell NEC', 'small cell carcinoma, oesophagus', 'esophagus small cell carcinoma', 'Oat cell carcinoma of the esophagus', 'small cell carcinoma, esophagus']",7134,,,C1112474,,C6762,,,,,,
mondo:0004117,ampulla of vater small cell neuroendocrine carcinoma,"['ampullary small cell carcinoma', 'ampulla of Vater small cell neuroendocrine carcinoma', 'ampulla of Vater small cell NEC', 'ampulla of Vater small cell carcinoma', 'small cell neuroendocrine carcinoma of the ampullary region', 'hepatopancreatic ampulla small cell carcinoma']",7136,,,C1332250,,C6655,,,,,,
mondo:0004118,cystitis cystica,,7138,,,C0152262,,C96230,,,595.81,,,
mondo:0004120,Bartholin gland small cell carcinoma,"['small cell carcinoma of major vestibular gland', 'Bartholin^s gland small cell carcinoma', 'Bartholin gland small cell carcinoma', 'major vestibular gland small cell carcinoma']",7140,,,C1511051,,C40298,,,,,,
mondo:0004122,thymus small cell carcinoma,"['small cell carcinoma of Thymus', 'Thymus small cell carcinoma', 'small cell carcinoma of the Thymus', 'thymus small cell carcinoma', 'thymic small cell carcinoma', 'thymic small cell carcinoma neuroendocrine type']",7142,,,C1335980,,C6460,1000578,,,,,
mondo:0004124,prostate stromal sarcoma,"['stromal sarcoma of the prostate', 'prostate stromal sarcoma', 'stromal sarcoma of prostate']",7152,,,C1335521,,C5524,,,,,,
mondo:0004125,rectum leiomyoma,"['leiomyoma of the rectum', 'rectal leiomyoma', 'rectum leiomyoma', 'leiomyoma of rectum']",7160,,,C1335682,,C5552,,,,,,
mondo:0004126,thyroiditis,"['thyroiditis', 'thyroid gland inflammation', 'thyroiditis (disease)']",7166,,,C0040147,,C26894,,D013966,245.9,,,0100646
mondo:0004127,lung occult adenocarcinoma,"['occult adenocarcinoma of lung', 'occult adenocarcinoma of the lung', 'occult lung adenocarcinoma']",7168,,,C1335096,,C6699,,,,,,
mondo:0004128,lung occult large cell carcinoma,"['occult large cell carcinoma of the lung', 'occult large cell lung carcinoma', 'occult large cell carcinoma of lung']",7169,,,C1335095,,C6685,,,,,,
mondo:0004129,cloacogenic carcinoma,"['anal cloacogenic carcinoma', 'cloacogenic carcinoma of the anus', 'cloacogenic anal carcinoma', 'cloacogenic carcinoma of anus', 'anal canal cloacogenic cancer', 'anal canal cloacogenic carcinoma', 'cloacogenic carcinoma', 'cloacogenic carcinoma (morphologic abnormality)']",7173,,,,,C8255,,C563020,,,,
mondo:0004130,anus basaloid carcinoma,"['anal basaloid carcinoma', 'basaloid carcinoma of the anus', 'basaloid carcinoma of anus', 'anus basaloid squamous cell carcinoma']",7174,,,C0280470,,C8256,,,,,,
mondo:0004131,anal verrucous carcinoma,"['anal Buschke-Lowenstein tumor', 'anal giant (malignant) condyloma', 'anal Buschke-Lowenstein tumour', 'anal verrucous carcinoma']",7175,,,C1332278,,C7470,,,,,,
mondo:0004132,anal canal squamous cell carcinoma,"['anal canal squamous cell carcinoma', 'squamous cell carcinoma of the anal canal']",7177,,424019,C1332262,,C7469,,,,,,
mondo:0004133,pituitary gland mixed eosinophil-basophil adenoma,"['mixed acidophil-basophil adenoma', 'pituitary gland mixed acidophil-basophil adenoma', 'mixed acidophil-basophil adenoma (morphologic abnormality)', 'mixed eosinophil-basophil adenoma']",7179,,,C0334312,,C4148,,,,,,
mondo:0004134,benign dermal neurilemmoma,"['benign schwannoma of the skin', 'benign dermal schwannoma', 'benign schwannoma of skin', 'benign skin neurilemmoma', 'benign neurilemmoma of the skin', 'benign skin schwannoma', 'benign neurilemmoma of skin']",7181,,,C1332490,,C5569,,,,,,
mondo:0004135,subacute lymphocytic thyroiditis,"['Subacute painless thyroiditis', 'Subacute lymphocytic thyroiditis', 'silent thyroiditis']",7187,,,C1306804,,C35829,,,,,,
mondo:0004136,ovarian endometrioid cystadenoma,['ovarian endometrioid cystadenoma'],7191,,,C1518713,,C40075,,,,,,
mondo:0004139,normocytic anemia,"['normocytic Anaemia', 'normocytic Anemia', 'anaemia normocytic', 'anemia normocytic']",720,,,C0085577,,C35142,,,285.8,,,
mondo:0004140,intermediate malignant teratoma,"['malignant teratoma, intermediate', 'malignant teratoma, intermediate (morphologic abnormality)', 'Intermediate immature teratoma']",7202,,,C0334522,,C4288,,,,,,
mondo:0004141,melanomatosis,['melanomatosis'],7206,,,C1334691,,C9499,,,,,,
mondo:0004142,lung combined large cell neuroendocrine carcinoma,"['combined large cell lung neuroendocrine carcinoma', 'combined large cell neuroendocrine carcinoma of the lung', 'pulmonary combined large cell neuroendocrine carcinoma', 'combined large cell neuroendocrine carcinoma of lung']",7207,,,C1333122,,C7267,,,,,,
mondo:0004143,psammomatous meningioma,['psammomatous meningioma (morphologic abnormality)'],7210,,,C0334607,,C4331,1000500,,,,,
mondo:0004144,fibrous meningioma,"['fibroblastic meningioma', 'fibrous meningioma (morphologic abnormality)']",7211,,,C0334606,,C4330,1000258,,,,,
mondo:0004145,meningothelial meningioma,"['Meningotheliomatous meningioma', 'meningothelial meningioma (morphologic abnormality)']",7212,,,C0334605,,C4329,1000372,,,,,
mondo:0004146,transitional meningioma,"['transitional (mixed) meningioma', 'transitional meningioma (morphologic abnormality)', 'mixed meningioma']",7213,,,C0334611,,C4333,1000602,,,,,
mondo:0004147,noninvasive malignant thymoma,"['malignant thymoma, noninvasive', 'thymoma malignant noninvasive']",7214,,,C0278847,,C9080,,,,,,
mondo:0004148,gallbladder papillary neoplasm with an associated invasive carcinoma,"['intracystic papillary neoplasm with an associated invasive carcinoma', 'papillary carcinoma of gallbladder', 'papillary carcinoma of the gallbladder', 'gallbladder papillary carcinoma', 'gallbladder papillary neoplasm with an associated invasive cancer', 'gallbladder papillary neoplasm with an associated invasive carcinoma', 'gall bladder papillary carcinoma']",7221,,,C1333753,,C5743,,,,,,
mondo:0004149,gallbladder pleomorphic giant cell adenocarcinoma,['pleomorphic giant cell adenocarcinoma of the gallbladder'],7222,,,,,,,,,,,
mondo:0004150,breast giant fibroadenoma,"['giant fibroadenoma of breast', 'breast giant fibroadenoma', 'giant fibroadenoma', 'giant fibroadenoma of the breast', 'giant breast fibroadenoma']",7223,,,C0346157,,C4273,,,,,,
mondo:0004151,spinal meninges cancer,"['malignant neoplasm of meninx of spinal cord', 'meninx of spinal cord cancer', 'cancer of meninx of spinal cord', 'malignant neoplasm of spinal meninges', 'malignant meninx of spinal cord neoplasm']",7224,,,C0153647,,,,,192.3,,,
mondo:0004152,chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation,"['postgerminal centre chronic lymphocytic leukemia/small lymphocytic lymphoma', 'postgerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma', 'CLL/SLL with IGVH SHM', 'chronic lymphocytic leukemia/small lymphocytic lymphoma with immunoglobulin heavy chain variable-region gene somatic hypermutation']",7230,,,C1333037,,C37201,,,,,,
mondo:0004153,childhood central nervous system embryonal carcinoma,"['embryonal carcinoma of the pediatric CNS', 'paediatric central nervous system embryonal carcinoma', 'embryonal carcinoma of the paediatric CNS', 'pediatric central nervous system embryonal carcinoma', 'embryonal carcinoma of paediatric CNS', 'embryonal carcinoma of the central nervous system of childhood', 'paediatric CNS embryonal cell carcinoma', 'embryonal carcinoma of paediatric central nervous system', 'pediatric CNS embryonal cell carcinoma', 'embryonal carcinoma of pediatric central nervous system', 'embryonal carcinoma of childhood central nervous system', 'embryonal carcinoma of the paediatric central nervous system', 'childhood CNS embryonal cell carcinoma', 'paediatric embryonal carcinoma of the central nervous system', 'embryonal carcinoma of childhood CNS', 'embryonal carcinoma of the childhood central nervous system', 'pediatric embryonal carcinoma of the central nervous system', 'embryonal carcinoma of the childhood CNS', 'childhood central nervous system embryonal carcinoma', 'embryonal carcinoma of the pediatric central nervous system', 'childhood embryonal carcinoma of the central nervous system', 'embryonal carcinoma of pediatric CNS']",7231,,,C1377605,,C6208,,,,,,
mondo:0004155,adult central nervous system embryonal carcinoma,"['embryonal carcinoma of the central nervous system of adults', 'adult embryonal carcinoma of the central nervous system', 'embryonal carcinoma of the adult CNS', 'adult CNS embryonal carcinoma', 'embryonal carcinoma of adult CNS', 'embryonal carcinoma of the adult central nervous system', 'adult central nervous system embryonal carcinoma', 'Central nervous system embryonal carcinoma', 'embryonal carcinoma of adult central nervous system']",7233,,,C1370503,,C5790,,,,,,
mondo:0004156,pancreatic mucinous cystadenocarcinoma,"['colloid Cystadencarcinoma of pancreas', 'colloidal Cystadencarcinoma of pancreas', 'mucinous Cystadencarcinoma of the pancreas', 'pancreatic mucinous cystadenocarcinoma', 'colloidal Cystadencarcinoma of the pancreas', 'colloid Cystadencarcinoma of the pancreas', 'mucinous Cystadencarcinoma of pancreas', 'pancreatic colloidal Cystadencarcinoma', 'pancreatic colloid Cystadencarcinoma', 'pancreatic colloid cystadenocarcinoma']",7234,,,C1335308,,C5713,,,,,,
mondo:0004158,pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma,"['pancreatic mucinous-cystic neoplasm with an associated invasive carcinoma', 'pancreatic mucinous cystic neoplasm with an associated invasive carcinoma', 'pancreatic invasive mucinous cystadenocarcinoma']",7236,,,C1518870,,C41246,,,,,,
mondo:0004159,pancreatic non-invasive mucinous cystadenocarcinoma,,7237,,,C1518874,,C41245,,,,,,
mondo:0004160,female stress incontinence,"['stress incontinence - female', 'female urinary stress incontinence']",724,,,C0038437,,C35042,,,625.6,,,
mondo:0004161,uterine corpus apoplectic leiomyoma,"['uterine corpus hemorrhagic cellular leiomyoma', 'uterine corpus leiomyoma with apoplectic change']",7241,,,C1519852,,C40165,,,,,,
mondo:0004162,uterine corpus cellular leiomyoma,"['body of uterus cellular leiomyoma', 'cellular leiomyoma of body of uterus', 'uterine corpus cellular leiomyoma']",7242,,,C1519845,,C40163,,,,,,
mondo:0004163,bladder urachal urothelial carcinoma,['bladder urachal urothelial carcinoma'],7244,,,C1511207,,C39844,,,,,,
mondo:0004164,lymphoepithelioma-like acinar prostate adenocarcinoma,"['lymphoepithelioma-like variant acinar prostate adenocarcinoma', 'acinar prostate adenocarcinoma, lymphoepithelioma-like variant']",7246,,,C1515864,,C39885,,,,,,
mondo:0004165,selective IgD deficiency disease,"['selective IgD immunodeficiency', 'selective immunoglobulin D deficiency']",7263,,,C0398695,,C27144,,,279.03,,,
mondo:0004166,hereditary fallopian tube carcinoma,"['hereditary fallopian tube carcinoma', 'familiar fallopian tube carcinoma', 'familial fallopian tube carcinoma', 'hereditary fallopian tube cancer']",7266,,,C1512418,,C40455,,,,,,
mondo:0004168,cribriform variant testicular seminoma,"['testicular seminoma, cribriform variant']",7269,,,C1515292,,C40957,,,,,,
mondo:0004169,premenstrual tension,,727,,,C0376356,,,,D011293,625.4,,,
mondo:0004170,nodular episcleritis,,728,,,C0155352,,,,,379.02,,,
mondo:0004172,uterine corpus adenocarcinofibroma,['body of uterus adenocarcinofibroma'],7281,,,,,,,,,,,
mondo:0004173,adenocarcinoma of skene gland origin,"['adenocarcinoma of Skene gland origin', 'carcinoma of paraurethral gland', 'Skene gland carcinoma', 'adenocarcinoma of Skene gland', 'paraurethral gland adenocarcinoma', 'paraurethral gland carcinoma', 'carcinoma of Skene^s gland', 'carcinoma of the paraurethral gland', 'carcinoma of Skene gland']",7284,,,C1527427,,C39863,,,,,,
mondo:0004174,secretory uterine corpus endometrioid adenocarcinoma,"['secretory uterine corpus endometrioid adenocarcinoma', 'endometrial endometrioid adenocarcinoma, secretory variant']",7289,,,C1336907,,C27839,,,,,,
mondo:0004175,mucin-rich endometrial endometrioid adenocarcinoma,,7293,,,C1513711,,C8717,,,,,,
mondo:0004176,childhood extraosseous osteosarcoma,"['childhood extraskeletal osteosarcoma', 'paediatric extraskeletal osteosarcoma', 'pediatric extraosseous osteosarcoma', 'childhood extraosseous osteosarcoma', 'pediatric extraskeletal osteosarcoma', 'paediatric extraosseous osteosarcoma', 'extraosseous osteosarcoma of childhood']",7297,,,C1332968,,C27376,,,,,,
mondo:0004177,benign urethral neoplasm,"['neoplasm. urethra', 'benign tumor of the urethra', 'urethra benign neoplasm', 'benign tumour of urethra', 'benign neoplasm of the urethra', 'benign urethra tumour', 'benign neoplasm of urethra', 'benign urethral neoplasm', 'benign urethral tumour', 'benign tumour of the urethra', 'benign tumor of urethra', 'urethral benign neoplasm', 'benign urethra neoplasm', 'benign urethral tumor', 'benign urethra tumor']",730,,,,,C3619,,,223.81,,,
mondo:0004178,"testicular yolk sac tumor, endodermal sinus pattern","['endodermal sinus pattern testicular yolk sac tumour', 'testicular yolk sac tumor, endodermal sinus pattern', 'endodermal sinus pattern testicular yolk sac tumor']",7302,,,C1515303,,C39927,,,,,,
mondo:0004180,benign urinary system neoplasm,"['neoplasm of urinary system', 'benign neoplasm of urinary tract', 'benign tumour of the urinary tract', 'benign urinary tract tumour', 'renal system benign neoplasm', 'tumor of urinary tract', 'tumor of the urinary system', 'urinary system benign neoplasm', 'tumour of urinary tract', 'benign urinary system neoplasm', 'benign urinary tract tumor', 'benign tumor of urinary tract', 'benign tumour of urinary tract', 'urinary tract neoplasm', 'benign urinary tract neoplasm', 'benign tumor of the urinary tract', 'tumour of the urinary system', 'benign neoplasm of the urinary tract']",731,,,,,C4893,,D014571,223.9,,,
mondo:0004181,breast adenomyoepithelial adenosis,,7312,,,C1511283,,C40391,,,,,,
mondo:0004182,stage IVb bladder cancer,"['stage IVB bladder cancer', 'Jewett-Marshall bladder cancer', 'Jewett-Marshall stage D1 bladder cancer', 'stage IVB urinary bladder cancer', 'Jewett-Marshall stage D2 urinary bladder cancer', 'Jewett-Marshall stage D2 bladder cancer', 'stage IVB urinary bladder carcinoma', 'Jewett-Marshall stage D2 urinary bladder carcinoma']",7315,,,C1336362,,C9368,,,,,,
mondo:0004183,axonal neuropathy,"['axon peripheral neuropathy', 'peripheral neuropathy of axon', 'axonal neuropathy']",7319,,,C0270921,,C27301,,,,,,
mondo:0004184,urethral disorder,"['disorder of urethra', 'urethra disease or disorder', 'disease of urethra', 'urethra disease', 'urethra disorder']",732,,,C0041969,,C26903,,D014522,,,,
mondo:0004185,ovarian serous cystadenofibroma,"['ovarian serous cystadenofibroma', 'ovary serous cystadenofibroma']",7320,,,C0877572,,C40032,,,,,,
mondo:0004186,cranial nodular fasciitis,"['cranial nodular fasciitis', 'cranial pseudosarcomatous fasciitis']",7326,,,C1333162,,C27248,,,,,,
mondo:0004187,nodular fasciitis,"['pseudosarcomatous fasciitis', 'fasciitis - nodular', 'pseudosarcomatous fibromatosis', 'nodular fasciitis']",7327,,477742,C0410005,,C3827,,,728.79,M72.4,,
mondo:0004188,iris spindle cell melanoma,"['spindle cell melanoma of the iris', 'spindle cell melanoma of iris', 'iris spindle cell melanoma']",7328,,,C1334287,,C6098,,,,,,
mondo:0004189,esophageal tuberculosis,"['tuberculosis of oesophagus', 'esophagus tuberculosis', 'tuberculosis of esophagus', 'oesophagus tuberculosis']",7332,,,C0152902,,,,,017.83,,,
mondo:0004190,nephrogenic adenoma of urinary bladder,"['nephrogenic adenoma of the urinary bladder', 'urinary bladder nephrogenic adenoma']",7333,,,C1336892,,C7415,,,,,,
mondo:0004191,nephrogenic adenoma,['nephrogenic adenoma'],7334,,,C0334039,,C7413,,,,,,
mondo:0004192,urethra cancer,"['malignant urethra tumor', 'malignant neoplasm of urethra', 'urethra cancer', 'malignant urethral tumour', 'malignant urethral neoplasm', 'malignant tumor of the urethra', 'malignant tumor of urethra', 'malignant tumour of urethra', 'malignant urethra neoplasm', 'malignant urethral tumor', 'malignant tumour of the urethra', 'urethral cancer', 'urethral Ca', 'cancer of urethra', 'malignant urethra tumour', 'malignant neoplasm of the urethra']",734,,,,,C7507,,,189.3,C68.0,,
mondo:0004193,pediatric ovarian dysgerminoma,"['childhood dysgerminoma', 'paediatric dysgerminoma of ovary', 'childhood ovarian germinomatous germ cell tumor', 'dysgerminoma of ovary of childhood', 'childhood ovarian germinomatous germ cell tumour', 'childhood ovarian dysgerminoma', 'pediatric dysgerminoma of ovary']",7340,,,C1332988,,C6550,,,,,,
mondo:0004194,ovarian stromal hyperthecosis,,7347,,,C1518743,,C40446,,,,,,
mondo:0004195,thymic dysplasia,,7350,,,C1331541,,C27802,,,,,,
mondo:0004196,rectal sarcomatoid carcinoma,"['rectal sarcomatoid cancer', 'rectal sarcomatoid carcinoma', 'rectum sarcomatoid carcinoma', 'rectal spindle cell carcinoma', 'sarcomatoid carcinoma of the rectum', 'sarcomatoid carcinoma of rectum']",7356,,,C1335689,,C5556,,,,,,
mondo:0004197,male urethral cancer,"['Male urethral malignant neoplasm', 'cancer of male urethra', 'male urethra cancer', 'malignant male urethra neoplasm', 'malignant neoplasm of male urethra']",736,,,C1518164,,C39867,,,,,,
mondo:0004198,"testicular yolk sac tumor, solid pattern","['solid pattern testicular yolk sac tumor', 'testicular yolk sac tumor, solid pattern', 'solid pattern testicular yolk sac tumour']",7360,,,C1515312,,C39925,,,,,,
mondo:0004199,vulvar keratinizing squamous cell carcinoma,['vulvar keratinizing squamous cell carcinoma'],7363,,,C2109334,,C40284,,,,,,
mondo:0004200,superficial urinary bladder carcinoma,"['superficial urinary bladder carcinoma', 'superficial bladder carcinoma', 'superficial urinary bladder cancer', 'superficial bladder cancer']",7371,,,C1336527,,C27474,,,,,,
mondo:0004201,pituitary hypoplasia,"['pituitary gland hypoplasia', 'pituitary hypoplasia']",7378,,,C0948740,,C27343,,,,,,
mondo:0004202,adrenal medulla carcinoma,"['adrenal medulla carcinoma', 'carcinoma of adrenal medulla']",7379,,,C1334717,,C9276,,,,,,
mondo:0004203,female urethral cancer,"['female urethra cancer', 'malignant neoplasm of female urethra', 'female urethral malignant neoplasm', 'cancer of female urethra', 'malignant female urethra neoplasm']",738,,,C1517154,,C39866,,,,,,
mondo:0004204,squamous cell skin papilloma,"['squamous cell papilloma of skin', 'zone of skin squamous papilloma', 'hyperkeratotic papilloma of skin', 'Dyskeratotic papilloma of the skin', 'squamous cell skin papilloma', 'Dyskeratotic papilloma of skin', 'parakeratotic papilloma of skin', 'parakeratotic papilloma of the skin', 'Dyskeratotic skin papilloma', 'parakeratotic skin papilloma', 'hyperkeratotic skin papilloma', 'squamous cell papilloma of the skin', 'hyperkeratotic papilloma of the skin']",7380,,,C0345983,,C4462,,,,,,
mondo:0004205,lymphohistiocytoid mesothelioma,,7381,,,C1334464,,C27779,,,,,,
mondo:0004206,pulmonary vein leiomyosarcoma,"['leiomyosarcoma of pulmonary vein', 'leiomyosarcoma of the pulmonary vein', 'pulmonary vein leiomyosarcoma']",7388,,,C1335575,,C5374,,,,,,
mondo:0004207,pulmonary artery leiomyosarcoma,"['pulmonary artery leiomyosarcoma', 'leiomyosarcoma of the pulmonary artery', 'leiomyosarcoma of pulmonary artery']",7389,,,C1335572,,C5373,,,,,,
mondo:0004208,superior vena cava leiomyosarcoma,"['anterior vena cava leiomyosarcoma', 'leiomyosarcoma of the Superior vena cava', 'leiomyosarcoma of Superior vena cava']",7390,,,C1336531,,C6745,,,,,,
mondo:0004209,cerebral primitive neuroectodermal tumor,"['primitive neuroectodermal neoplasm of the cerebrum', 'cerebral hemisphere primitive neuroectodermal tumor', 'cerebral hemisphere primitive neuroectodermal tumour', 'cerebral hemisphere PNET', 'cerebral PNET', 'primitive neuroectodermal tumor of cerebral hemispheres', 'cerebral hemisphere primitive neuroectodermal neoplasm', 'primitive neuroectodermal neoplasm of the cerebral hemispheres', 'PNET of the cerebrum', 'primitive neuroectodermal neoplasm of cerebrum', 'PNET of cerebrum', 'primitive neuroectodermal tumour of cerebrum', 'primitive neuroectodermal tumour of the cerebrum', 'primitive neuroectodermal tumor of cerebrum', 'primitive neuroectodermal tumour of cerebral hemispheres', 'primitive neuroectodermal tumor of the cerebral hemispheres', 'primitive neuroectodermal tumour of the cerebral hemispheres', 'PNET of cerebral hemispheres', 'PNET of the cerebral hemispheres', 'primitive neuroectodermal tumor of the cerebrum', 'cerebral primitive neuroectodermal tumor', 'cerebral primitive neuroectodermal neoplasm', 'primitive neuroectodermal neoplasm of cerebral hemispheres']",7398,,,C0751675,,C4970,,,,,,
mondo:0004210,colonic L-cell glucagon-like peptide producing tumor,"['colon L-cell glucagon-like peptide-producing neuroendocrine tumor', 'L-cell glucagon-like peptide-producing neuroendocrine tumor of colon', 'colon L-cell glucagon-like peptide-producing NET', 'L-cell glucagon-like peptide-producing neuroendocrine tumour of colon', 'colonic L-cell glucagon-like peptide-producing neuroendocrine tumour', 'colonic L-cell glucagon-like peptide-producing neuroendocrine tumor', 'colon L-cell glucagon-like peptide-producing neuroendocrine tumour']",7401,,,C3274139,,C27447,,,,,,
mondo:0004211,L-cell glucagon-like peptide-producing neuroendocrine tumor,"['L-cell glucagon-like peptide producing tumor', 'L-cell glucagon-like peptide-producing neuroendocrine tumor', 'L-cell glucagon-like peptide producing tumour', 'L-cell glucagon-like peptide-producing NET']",7402,,,C3274140,,C27448,,,,,,
mondo:0004212,vulvar keratoacanthoma-like carcinoma,"['vulvar squamous cell carcinoma, keratoacanthoma type']",7408,,,C1520086,,C40288,,,,,,
mondo:0004213,vulvar non-keratinizing squamous cell carcinoma,,7409,,,C1520092,,C40285,,,,,,
mondo:0004214,ovarian endometrioid cystadenofibroma,['ovarian endometrioid cystadenofibroma'],7411,,,C1335158,,C27288,,,,,,
mondo:0004215,cutaneous anthrax,"['skin anthrax', 'anthrax, skin type']",7426,,,C0003177,,,,C531621,022.0,A22.0,,
mondo:0004216,pineal region germinoma,"['pineal germinoma', 'germinoma']",7428,,91352,C0854912,,C8712,,,,,,
mondo:0004217,childhood brain germinoma,"['germinoma of the childhood brain', 'pediatric brain germ cell cancer', 'paediatric brain germinoma', 'germinoma of the pediatric brain', 'paediatric brain germ cell cancer', 'brain germinoma of childhood', 'germinoma of pediatric brain', 'germinoma of childhood brain', 'germinoma of paediatric brain', 'pediatric brain germinoma', 'germinoma of the paediatric brain']",7429,,,C1332948,,C6207,,,,,,
mondo:0004218,childhood germ cell brain tumor,"['Brain germ cell tumour', 'germ cell neoplasm of the paediatric brain', 'germ cell neoplasm of the childhood brain', 'germ cell neoplasm of childhood brain', 'childhood brain germ cell neoplasm', 'germ cell tumor of the pediatric brain', 'germ cell tumor of the childhood brain', 'pediatric brain germ cell neoplasm', 'germ cell tumor of childhood brain', 'pediatric brain germ cell tumor', 'germ cell neoplasm of pediatric brain', 'Brain germ cell tumor', 'germ cell tumour of the childhood brain', 'paediatric brain germ cell tumour', 'germ cell neoplasm of the pediatric brain', 'childhood germ cell brain neoplasm', 'childhood brain germ cell tumour', 'germ cell neoplasm of paediatric brain', 'germ cell tumor of pediatric brain', 'germ cell tumour of the paediatric brain', 'germ cell tumour of childhood brain', 'childhood brain germ cell tumor', 'paediatric brain germ cell neoplasm', 'germ cell tumour of paediatric brain']",7430,,,C1377598,,C5795,,,,,,
mondo:0004219,polyvesicular vitelline pattern testicular yolk sac tumor,"['testicular yolk Sac tumor, polyvesicular vitelline pattern']",7435,,,C1515311,,C39930,,,,,,
mondo:0004220,endometrial endometrioid adenocarcinoma with spindled epithelial cells,"['endometrial endometrioid adenocarcinoma with spindled epithelial cells', 'sarcomatoid uterine corpus endometrioid adenocarcinoma']",7436,,,C1336913,,C27850,,,,,,
mondo:0004221,uterine corpus perivascular epithelioid cell tumor,"['uterus perivascular epithelioid cell tumor', 'uterine corpus PEComa', 'body of uterus neoplasm with perivascular epithelioid cell differentiation', 'uterine perivascular epithelioid cell tumour', 'uterine corpus perivascular epithelioid cell tumor', 'uterine perivascular epithelioid cell tumor', 'uterus perivascular epithelioid cell tumour']",7437,,,C1519862,,C40180,,,,,,
mondo:0004222,ovarian clear cell cystadenocarcinoma,['ovarian clear cell cystadenocarcinoma'],7438,,,C0279667,,C7980,,,,,,
mondo:0004223,polyp of middle ear,"['middle ear polyp', 'polyp - middle ear', 'middle Ear polyp', 'polyp of the middle ear']",7439,,,C0271466,,C6933,,,,H74.4,,
mondo:0004224,chronic metabolic polyneuropathy,['chronic metabolic polyneuropathy'],7441,,,C1333042,,C35602,,,,,,
mondo:0004225,monoclonal gammopathy of uncertain significance,"['MGUS', 'monoclonal gammopathy Of undetermined significance (MGUS)', 'monoclonal gammopathy of undetermined significance', 'monoclonal gammopathy of undetermined significance (MGUS)', 'monoclonal gammopathy of undetermined significance (morphologic abnormality)', 'monoclonal gammopathy, benign', 'monoclonal gammopathy of unknown significance', 'benign monoclonal gammopathy']",7442,,,C0026470,,C3996,1000836,D008998,238.6,,,
mondo:0004226,diffuse intraductal papillomatosis,['diffuse intraductal papillomatosis'],7444,,,C1377912,,C7364,,,,,,
mondo:0004227,epididymal adenomatoid tumor,"['adenomatoid tumor of the epididymis', 'adenomatoid neoplasm of epididymis', 'epididymal adenomatoid tumor', 'adenomatoid tumour of the epididymis', 'adenomatoid tumor of epididymis', 'adenomatoid tumour of epididymis', 'benign epididymal epithelial mesothelioma', 'epididymis adenomatoid tumour', 'epididymis adenomatoid tumor', 'adenomatoid neoplasm of the epididymis']",745,,,C1333415,,C6382,,,,,,
mondo:0004229,acantholytic variant squamous cell breast carcinoma,"['squamous cell breast carcinoma, acantholytic variant']",7459,,,C1519485,,C40359,1001969,,,,,
mondo:0004230,adenomatoid tumor,"['adenomatoid tumour NOS (morphologic abnormality)', 'benign tumor of mesothelium', 'adenomatoid tumor (morphologic abnormality)', 'benign neoplasm of the mesothelium', 'benign tumour of the mesothelium', 'adenomatoid tumor', 'benign localised epithelial mesothelioma', 'adenomatoid tumour (morphologic abnormality)', 'benign localized epithelial mesothelioma', 'adenomatoid tumor NOS (morphologic abnormality)', 'mesothelioma, benign', 'benign mesothelial neoplasm', 'benign mesothelial tumor', 'benign mesothelial tumour', 'benign neoplasm of mesothelium', 'adenomatoid tumor, benign', 'benign tumour of mesothelium', 'benign mesothelioma', 'benign tumor of the mesothelium']",746,,,C0206675,,C3762,,D018254,,,,
mondo:0004231,spindle cell variant squamous cell breast carcinoma,"['squamous cell breast carcinoma, spindle cell variant', 'metaplastic adenocarcinoma with spindle cell differentiation']",7460,,,C1519487,,C40358,,,,,,
mondo:0004232,large cell keratinizing variant squamous cell breast carcinoma,"['squamous cell breast carcinoma, large cell keratinizing variant']",7461,,,C1519486,,C40357,,,,,,
mondo:0004233,childhood pleomorphic rhabdomyosarcoma,"['childhood anaplastic rhabdomyosarcoma', 'paediatric pleomorphic rhabdomyosarcoma', 'Pleomorphic rhabdomyosarcoma', 'pleomorphic rhabdomyosarcoma of childhood', 'pediatric pleomorphic rhabdomyosarcoma', 'pleomorphic childhood rhabdomyosarcoma']",7463,,,C0279614,,C7959,,,,,,
mondo:0004234,chronic lymphoproliferative disorder of NK-cells,"['chronic NK-large granular lymphocyte lymphoproliferative disorder', 'NK-LGL leukemia', 'NK-cell large granular lymphocyte lymphocytosis', 'natural killer-cell large granular lymphocyte leukaemia', 'indolent NK-cell lymphoproliferative disorder', 'natural killer-cell large granular lymphocyte leukemia', 'CNKL', 'chronic lymphoproliferative disorder of natural killer cells', 'chronic NK-cell lymphocytosis', 'chronic lymphoproliferative disorder of NK-cells', 'indolent large granular NK-cell lymphoproliferative disorder', 'NK-cell lineage granular lymphocyte proliferative disorder', 'NK-LGLL', 'NK-type lymphoproliferative disorder of granular lymphocytes', 'CLPD-NK', 'chronic NK-LGL lymphoproliferative disorder', 'chronic NK lymphocytosis', 'NK-LGL leukaemia']",7465,,512017,C1512709,,C39591,,,,,,
mondo:0004235,diverticulitis,['digestive tract diverticulum inflammation'],7475,,,C0012813,,C26752,1001460,D004238,,,,
mondo:0004236,duodenal somatostatinoma,"['duodenal somatostatin producing tumor', 'duodenal somatostatin-producing neuroendocrine tumour', 'duodenal somatostatin-producing NET', 'duodenal somatostatinoma', 'duodenal delta cell somatostatin producing tumour', 'duodenal somatostatin-producing neuroendocrine tumor', 'duodenal delta cell somatostatin producing tumor', 'duodenal somatostatin producing tumour']",7479,,,C1333320,,C27407,,,,,,
mondo:0004237,large cell carcinoma with rhabdoid phenotype,"['large cell lung carcinoma with rhabdoid phenotype', 'large cell carcinoma with rhabdoid phenotype (morphologic abnormality)', 'RLCLC']",7480,,,C1265997,,C6876,,,,,,
mondo:0004238,petrous apex meningioma,"['meningioma of the petrous apex', 'petrous ridge meningioma', 'meningioma of petrous ridge', 'meningioma of the petrous ridge', 'meningioma of petrous apex']",7482,,,C1335396,,C5271,,,,,,
mondo:0004239,cervical keratinizing squamous cell carcinoma,['cervical keratinizing squamous cell carcinoma'],7483,,,C1517658,,C40187,,,,,,
mondo:0004240,posterior urethra cancer,"['malignant tumor of the posterior urethra', 'posterior urethral malignant tumour', 'posterior urethral cancer', 'malignant neoplasm of posterior urethra', 'posterior urethra malignant neoplasm', 'malignant tumour of the posterior urethra', 'posterior urethral malignant tumor', 'malignant neoplasm of the posterior urethra', 'malignant tumor of posterior urethra', 'posterior urethra malignant tumor', 'posterior urethra malignant tumour', 'malignant tumour of posterior urethra', 'posterior urethral malignant neoplasm']",7488,,,C0279931,,C7640,,,,,,
mondo:0004241,Osgood-Schlatter disease,"['osteochondritis of the tibial tubercle', 'aseptic necrosis of the tibial tubercle', 'Osteochondrosis of the tibial tubercle', 'juvenile osteochondrosis of tibial tubercle', 'osteochondritis of tibial tubercle', 'Osgood-Schlatter disease', 'Osteochondrosis of proximal tibia', 'Osgood-Schlatter^s disease']",7489,,97335,,,C34874,,,736.89,,10031130,
mondo:0004242,active peptic ulcer disease,['GI bleeding'],749,,,,,,,,578.9,,,
mondo:0004243,vulvar proximal-type epithelioid sarcoma,,7491,,,C1520093,,C40319,,,,,,
mondo:0004244,proximal-type epithelioid sarcoma,"['PTES', 'proximal-type epithelioid sarcoma', 'central epithelioid sarcoma']",7492,,,C1335563,,C27472,,,,,,
mondo:0004245,ependymal tumor of brain,"['brain ependymal tumor', 'ependymal tumor of brain', 'brain ependymoma', 'brain ependymal tumour', 'ependymoma of brain']",7497,,,C0238029,,C3861,,,,,,
mondo:0004247,peptic ulcer disease,"['acute peptic ulcer with haemorrhage and perforation', 'acute peptic ulcer with haemorrhage', 'acute peptic ulcer with hemorrhage', 'acute peptic ulcer with hemorrhage and perforation', 'peptic ulcer', 'acute peptic ulcer without hemorrhage and without perforation', 'acute peptic ulcer without haemorrhage and without perforation']",750,,,C0030920,,C3318,,D010437,533,,,
mondo:0004248,pediatric infratentorial ependymoma,"['childhood infratentorial ependymoma', 'pediatric infratentorial ependymoma', 'infratentorial ependymoma']",7501,,,C0278599,,C9041,,,,,,
mondo:0004249,pediatric supratentorial ependymoma,"['supratentorial ependymoma', 'pediatric cerebral ependymoma', 'paediatric cerebral ependymoma', 'paediatric supratentorial ependymoblastoma', 'pediatric supratentorial ependymoblastoma', 'childhood supratentorial ependymoma']",7502,,,C0278650,,C9043,0008495,,,,,
mondo:0004250,extrahepatic bile duct papillary adenoma,"['extrahepatic bile duct papillary adenoma', 'papillary adenoma of extrahepatic bile duct', 'papillary adenoma of the extrahepatic bile duct']",7503,,,C1333510,,C5849,,,,,,
mondo:0004251,small intestine neoplasm,"['small intestinal neoplasm', 'tumour of small bowel', 'tumour of small intestine', 'tumor of the small bowel', 'small intestine neoplasm', 'small bowel tumour', 'tumor of small intestine', 'tumor of the small intestine', 'tumour of the small intestine', 'neoplasm of the small bowel', 'small intestine tumour', 'tumor of small bowel', 'small bowel tumor', 'tumour of the small bowel', 'neoplasm of small intestine', 'neoplasm of the small intestine', 'small intestine tumor', 'small bowel neoplasm', 'small intestine neoplasm (disease)', 'neoplasm of small bowel']",7505,,,C0345832,,C4432,,,,,,
mondo:0004252,small intestinal L-cell glucagon-like peptide producing tumor,"['small intestinal L-cell, glucagon-like peptide-producing neuroendocrine tumour', 'small intestine L-cell glucagon-like peptide-producing neuroendocrine tumor', 'small intestinal L-cell glucagon-like peptide-producing neuroendocrine tumour', 'L-cell glucagon-like peptide-producing neuroendocrine tumour of small intestine', 'small intestinal L-cell glucagon-like peptide-producing neuroendocrine tumor', 'small intestinal L-cell glucagon-like peptide-producing NET', 'small intestine L-cell glucagon-like peptide-producing neuroendocrine tumour', 'small intestinal L-cell, glucagon-like peptide-producing neuroendocrine tumor', 'L-cell glucagon-like peptide-producing neuroendocrine tumor of small intestine']",7506,,,C3274143,,C27452,,,,,,
mondo:0004253,intraductal breast papillomatosis,"['intraductal papillomatosis of the breast', 'intraductal breast papillomatosis', 'intraductal papillomatosis of breast', 'breast intraductal papillomatosis']",7511,,,C1334247,,C5201,,,,,,
mondo:0004254,focal intraductal papillomatosis,"['localised intraductal papillomatosis', 'focal intraductal papillomatosis', 'localized intraductal papillomatosis']",7512,,,C1333626,,C7365,,,,,,
mondo:0004255,Wolffian adnexal tumor,"['female adnexal tumour of probable Wolffian origin', 'Wolffian tumour', 'WAT', 'FATWO', 'Wolffian tumor', 'Wolffian adnexal tumor', 'Wolffian adnexal neoplasm', 'Wolffian adenoma', 'female adnexal tumor of probable Wolffian origin']",7514,,,C1520159,,C40141,,C536741,,,,
mondo:0004256,lumbar spinal canal and spinal cord meningioma,"['meningioma of the lumbar spinal canal and spinal cord', 'lumbar intraspinal meningioma', 'meningioma of lumbar spinal canal and spinal cord']",7515,,,C1334436,,C5298,,,,,,
mondo:0004257,childhood central nervous system mixed germ cell tumor,"['childhood mixed germ cell tumour of central nervous system', 'Central nervous system Mixed germ cell tumour', 'childhood mixed germ cell tumor of central nervous system', 'Central nervous system Mixed germ cell tumor', 'pediatric mixed germ cell tumor of central nervous system', 'mixed germ cell tumour of central nervous system of childhood', 'mixed germ cell tumor of central nervous system of childhood', 'paediatric mixed germ cell tumour of central nervous system']",7516,,,C1332956,,C27403,,,,,,
mondo:0004258,female orgasmic disorder,"['female orgasmic disorder', 'inhibited female orgasm']",7518,,,,,C34958,,,302.73,F52.31,,
mondo:0004259,endocervical carcinoma,"['endocervical carcinoma', 'carcinoma of the endocervix', 'endocervical cancer', 'endocervix carcinoma', 'carcinoma of endocervix', 'endocervical adenocarcinoma']",7519,,,C1299237,,C28327,,,,,,
mondo:0004260,peptic ulcer perforation,"['perforated peptic ulcer', 'acute peptic ulcer with perforation', 'peptic ulcer with perforation']",752,,,C0267291,,,1001389,D010439,,,,
mondo:0004261,periductal breast myoepitheliosis,['periductal breast myoepitheliosis'],7520,,,C1518974,,C40388,,,,,,
mondo:0004262,breast myoepitheliosis,['breast myoepitheliosis'],7521,,,C1513799,,C40385,,,,,,
mondo:0004263,pediatric infratentorial ependymoblastoma,"['childhood infratentorial embryonal tumor with Multilayered Rosettes, C19MC-altered', 'childhood infratentorial ependymoblastoma', 'childhood infratentorial embryonal tumour with Multilayered Rosettes, C19MC-altered', 'pediatric infratentorial ependymoblastoma']",7522,,,C1332972,,C6773,,,,,,
mondo:0004264,acute gonococcal endometritis,"['uterus - acute gonorrhea', 'gonococcal endometritis (acute)', 'uterus - acute gonorrhoea', 'acute gonorrhoea of uterus', 'gonococcal endometritis', 'acute gonorrhea of uterus']",7527,,,C0341829,,,,,098.16,,,
mondo:0004265,acute endometritis,"['endometritis, acute']",7528,,,C0238103,,C27022,,,615.0,,,
mondo:0004266,anal gland adenocarcinoma,"['adenocarcinoma of anal ducts', 'adenocarcinoma of anal gland', 'adenocarcinoma of the anal gland', 'anal glands adenocarcinoma']",7531,,,C1266027,,C5609,,,,,,
mondo:0004267,squamous papillomatosis,['squamous papillomatosis'],7532,,,C1378340,,C9009,,,,,,
mondo:0004269,breast cystic hypersecretory carcinoma,"['cystic hypersecretory duct carcinoma of the breast', 'cystic hypersecretory carcinoma of the breast']",7537,,,,,,,,,,,
mondo:0004270,breast ductal adenoma,"['ductal adenoma', 'breast ductal adenoma']",7538,,,C1511307,,C40384,,,,,,
mondo:0004271,pregnancy adenoma,"['Lactating adenoma (morphologic abnormality)', 'Lactating adenoma']",7539,,,C1266023,,C9473,,,,,,
mondo:0004272,urinary bladder tuberculosis,"['bladder tuberculous', 'bladder tuberculosis', 'urinary bladder tuberculosis', 'tuberculosis of bladder, unspecified examination', 'tuberculous cystitis', 'tuberculosis of bladder']",754,,,C0152793,,,,,016.14,,,
mondo:0004273,breast apocrine adenoma,"['apocrine adenoma of breast', 'breast apocrine adenoma']",7540,,,C1388299,,C40383,,,,,,
mondo:0004274,mixed epithelial/mesenchymal metaplastic breast carcinoma,"['mixed type metaplastic breast cancer', 'breast carcinosarcoma']",7541,,,C1513365,,C40364,,,,,,
mondo:0004275,osteosarcoma arising in bone Paget disease,"['Paget osteosarcoma', 'osteosarcoma arising in osseous Paget^s disease', 'osteosarcoma arising in osteitis deformans', 'Paget^s osteosarcoma', 'osteosarcoma arising in bone Paget disease', 'osteosarcoma arising in bone Paget^s disease', 'osteosarcoma arising in Paget disease of bone', 'osteosarcoma arising in Paget^s disease of bone']",7542,,,C1335148,,C6469,,,,,,
mondo:0004276,ceruminoma,"['adenoma, ceruminous gland, benign', 'ceruminous adenoma', 'external auditory canal ceruminous adenoma', 'ceruminous adenoma of external auditory canal', 'ceruminous adenoma of the external auditory canal', 'ceruminous adenoma (morphologic abnormality)']",7549,,,C1333488,,C6088,,,,,,
mondo:0004277,gonorrhea,"['PAS', 'infections, Neisseria gonorrhoeae', 'Gianotti Crosti syndrome', 'PAC', 'Crosti-gianotti syndrome', 'chronic gonococcal infectious disease of upper genitourinary tract', 'acrodermatitis, papular infantile', 'papular acrodermatitis of childhood', 'acrodermatitis, infantile lichenoid', 'GC', 'Neisseria gonorrhoeae infection', 'chronic gonococcal infectious disease of lower genitourinary tract']",7551,,100642,C0018081,,C92950,,D006069,098.89,,,
mondo:0004278,infiltrating bladder urothelial carcinoma sarcomatoid variant,"['infiltrating bladder urothelial carcinoma sarcomatoid variant', 'infiltrating bladder urothelial carcinoma, sarcomatoid variant with heterologous elements', 'sarcomatoid carcinoma of the urinary bladder', 'infiltrating bladder urothelial carcinoma, sarcomatoid variant without heterologous elements']",7553,,,C1512745,,C39824,1000303,,,,,
mondo:0004279,glossopharyngeal motor neuropathy,"['glossopharyngeal nerve motor peripheral neuropathy', 'motor peripheral neuropathy of glossopharyngeal nerve']",7558,,,C0751942,,C27212,,,,,,
mondo:0004280,asymmetric motor neuropathy,,7559,,,C1332341,,C27953,,,,,,
mondo:0004281,vulvar eccrine porocarcinoma,"['mammalian vulva eccrine porocarcinoma', 'eccrine porocarcinoma of mammalian vulva', 'vulvar eccrine porocarcinoma']",7565,,,C1520081,,C40306,,,,,,
mondo:0004283,vulvar clear cell hidradenocarcinoma,['vulvar clear cell hidradenocarcinoma'],7567,,,C1520076,,C40307,,,,,,
mondo:0004285,pancreatic intraductal papillary-mucinous carcinoma,"['pancreatic intraductal papillary-colloidal carcinoma', 'intraductal papillary-colloid carcinoma of the pancreas', 'intraductal papillary-colloidal carcinoma of pancreas', 'intraductal papillary-mucinous carcinoma of pancreas', 'pancreatic intraductal papillary-mucinous carcinoma', 'intraductal papillary-colloidal carcinoma of the pancreas', 'intraductal papillary-mucinous carcinoma of the pancreas', 'intraductal papillary-colloid carcinoma of pancreas', 'pancreatic intraductal papillary mucinous carcinoma', 'pancreatic intraductal papillary-colloid carcinoma', 'intraductal papillary mucinous carcinoma of pancreas']",7574,,424058,C1335304,,C5725,,,,,,
mondo:0004286,pancreatic intraductal papillary-mucinous neoplasm,"['pancreatic intraductal papillary-mucinous neoplasm', 'pancreatic IPMN', 'IPMN', 'pancreatic intraductal papillary-mucinous tumour', 'intraductal papillary mucinous neoplasm', 'pancreatic intraductal papillary-mucinous tumor']",7575,,,C1518869,,C38342,,,,,,
mondo:0004287,pancreatic foamy gland adenocarcinoma,['pancreatic foamy gland adenocarcinoma'],7577,,,C1335303,,C37256,,,,,,
mondo:0004288,scirrhous breast carcinoma,"['scirrhous breast carcinoma', 'scirrhous carcinoma of breast', 'scirrhous carcinoma of the breast', 'infiltrating carcinoma of the breast with fibrotic Stroma', 'breast scirrhous carcinoma', 'infiltrating carcinoma of breast with fibrotic Stroma']",7578,,,C0346151,,C7362,,,,,,
mondo:0004289,glottis verrucous carcinoma,"['glottis verrucous carcinoma', 'verrucous carcinoma of the glottis', 'verrucous carcinoma of glottis', 'glottic verrucous carcinoma']",7583,,,C0280329,,C8189,,,,,,
mondo:0004290,subglottis verrucous carcinoma,"['subglottic verrucous carcinoma', 'subglottis verrucous carcinoma', 'verrucous carcinoma of the subglottis', 'verrucous carcinoma of subglottis']",7584,,,C0280330,,C8190,,,,,,
mondo:0004291,subglottis squamous cell carcinoma,"['subglottic epidermoid carcinoma', 'epidermoid carcinoma of the subglottis', 'epidermoid carcinoma of subglottis', 'squamous cell carcinoma of the subglottis', 'squamous cell carcinoma of subglottis', 'subglottis epidermoid carcinoma', 'subglottis squamous cell carcinoma', 'subglottic squamous cell carcinoma']",7585,,,C0280326,,C8187,,,,,,
mondo:0004292,supraglottis verrucous carcinoma,"['supraglottis verrucous carcinoma', 'verrucous carcinoma of the supraglottis', 'supraglottic verrucous carcinoma', 'supraglottic part of larynx verrucous carcinoma', 'verrucous carcinoma of supraglottis']",7586,,,C0280331,,C8191,,,,,,
mondo:0004293,supraglottis squamous cell carcinoma,"['epidermoid carcinoma of supraglottis', 'supraglottis epidermoid carcinoma', 'squamous cell carcinoma of the supraglottis', 'supraglottic part of larynx squamous cell carcinoma', 'squamous cell carcinoma of supraglottis', 'supraglottis squamous cell carcinoma', 'epidermoid carcinoma of the supraglottis', 'supraglottic epidermoid carcinoma', 'supraglottic squamous cell carcinoma']",7587,,,C0749163,,C4945,,,,,,
mondo:0004294,gestational ovarian choriocarcinoma,['gestational ovarian choriocarcinoma'],7591,,,C1517538,,C40442,,,,,,
mondo:0004295,asbestos-related lung carcinoma,"['asbestos-related lung carcinoma', 'asbestos-related lung cancer']",7596,,,C1332337,,C27925,,,,,,
mondo:0004296,cervical lymphoepithelioma-like carcinoma,['cervical lymphoepithelioma-like carcinoma'],7598,,,C1516418,,C40193,,,,,,
mondo:0004297,lymphoepithelioma-like thymic carcinoma,"['lymphoepithelial cancer of the Thymus', 'lymphoepithelial Thymus cancer', 'lymphoepithelioma-like carcinoma of the Thymus', 'lymphoepithelial cancer of Thymus', 'lymphoepithelioma-like carcinoma of Thymus', 'lymphoepithelioma-like Thymus carcinoma', 'lymphoepithelioma-like thymic carcinoma', 'thymic lymphoepithelioma-like carcinoma', 'malignant lymphoepithelial thymoma']",7599,,,C0279706,,C7998,,,,,,
mondo:0004298,stomach disorder,"['stomach disorder', 'stomach disease or disorder', 'gastric disease', 'disorder of stomach', 'stomach disease', 'disease of stomach', 'gastropathy']",76,,,C0038354,,C26886,,D013272,537.9,,,
mondo:0004299,infiltrating bladder lymphoepithelioma-like carcinoma,['infiltrating bladder lymphoepithelioma-like carcinoma'],7600,,,C1512736,,C39821,1000302,,,,,
mondo:0004301,fibrosarcomatous osteosarcoma,"['fibroblastic osteogenic sarcoma', 'fibroblastic osteosarcoma', 'fibrosarcomatous osteosarcoma', 'fibroblastic osteosarcoma (morphologic abnormality)', 'fibrosarcomatous osteogenic sarcoma', 'FIOS']",7603,,,C0279602,,C4020,,,,,,
mondo:0004302,chief cell adenoma,"['parathyroid chief cell adenoma', 'chief cell adenoma of the parathyroid gland', 'chief cell adenoma of parathyroid gland', 'chief cell adenoma', 'parathyroid gland chief cell adenoma', 'chief cell adenoma of the parathyroid', 'chief cell adenoma of parathyroid']",7607,,,C0334320,,C4154,,,,,,
mondo:0004303,parathyroid gland clear cell adenoma,"['clear cell adenoma of parathyroid', 'clear cell adenoma of the parathyroid', 'clear cell adenoma of parathyroid gland', 'transitional clear cell adenoma of the parathyroid gland', 'clear cell adenoma of the parathyroid gland', 'parathyroid gland clear cell adenoma', 'transitional clear cell adenoma of the parathyroid', 'parathyroid gland transitional clear cell adenoma', 'transitional clear cell adenoma of parathyroid', 'transitional clear cell adenoma of parathyroid gland', 'parathyroid clear cell adenoma', 'parathyroid transitional clear cell adenoma']",7609,,,C0279700,,C7993,,,,,,
mondo:0004304,mixed cell type adenoma of parathyroid,"['mixed cell type adenoma of the parathyroid gland', 'mixed cell type adenoma of parathyroid', 'parathyroid mixed cell type adenoma', 'mixed cell type adenoma of the parathyroid', 'mixed cell type adenoma of parathyroid gland', 'parathyroid gland mixed cell type adenoma']",7610,,,C0279701,,C7994,,,,,,
mondo:0004305,parathyroid oncocytic adenoma,"['parathyroid gland oncocytic adenoma', 'parathyroid oncocytic adenoma']",7611,,,C1335351,,C27393,,,,,,
mondo:0004306,childhood intracortical osteosarcoma,"['childhood conventional osteosarcoma', 'childhood intracortical osteosarcoma']",7612,,,C1332974,,C6590,,,,,,
mondo:0004307,sarcomatosis of the meninges,"['meningeal cluster sarcomatosis', 'meningeal sarcomatosis', 'sarcomatosis of the meninges', 'meninges sarcomatosis', 'meningeal sarcomatosis (morphologic abnormality)', 'sarcomatosis of meninges']",7613,,,C0334612,,C4334,,,,,,
mondo:0004308,meningeal sarcoma,"['meningeal cluster sarcoma', 'sarcoma of meningeal cluster', 'sarcoma of the meninges', 'sarcoma of meninges', 'meninges sarcoma', 'meningeal sarcoma']",7614,,,C0302327,,C4073,,,,,,
mondo:0004309,sarcomatosis,"['sarcomatosis', 'sarcomatosis (morphologic abnormality)', 'sarcomatosis NOS (morphologic abnormality)']",7615,,,C0334451,,C4243,,,,,,
mondo:0004310,"adult embryonal tumor with multilayered rosettes, c19mc-altered","['ependymoblastoma of adults', 'embryonal tumour with multilayered rosettes, C19MC-altered', 'adult embryonal tumor with multilayered rosettes, C19MC-altered', 'embryonal tumor with multilayered rosettes, C19MC-altered', 'adult ependymoblastoma', 'adult embryonal tumour with multilayered rosettes, C19MC-altered']",7631,,,C0281330,,C8290,,,,,,
mondo:0004311,carcinoma of Cowper glands,"['carcinoma of bulbo-urethral gland', 'Cowper gland carcinoma', 'bulbo-urethral gland carcinoma', 'carcinoma of Cowper glands']",7632,,,C1516284,,C39864,,,,,,
mondo:0004312,suprasellar meningioma,['sella turcica meningioma (disease)'],7634,,,C1336535,,C6776,,,,,,
mondo:0004313,gasserian ganglion meningioma,"['meningioma of Gasserian ganglion', 'Gasserian meningioma', 'gasserian ganglion meningioma (disease)', 'meningioma of the Gasserian ganglion']",7635,,,C1333760,,C6779,,,,,,
mondo:0004314,malignant cutaneous granular cell skin tumor,"['malignant granular cell skin tumour', 'malignant granular cell tumour of skin', 'malignant granular cell skin tumor', 'malignant granular cell skin neoplasm', 'malignant granular cell tumor of skin', 'malignant granular cell tumour of the skin', 'malignant granular cell neoplasm of the skin', 'malignant cutaneous granular cell tumor', 'malignant granular cell neoplasm of skin', 'malignant granular cell tumor of the skin', 'malignant cutaneous granular cell tumour']",7639,,,C1334575,,C5614,,,,,,
mondo:0004315,cholangiolocellular carcinoma,"['CLC', 'cholangiocarcinoma of intralobular bile duct', 'cholangiolocellular carcinoma', 'intralobular bile duct cholangiocarcinoma']",7642,,,C1516490,,C41617,,,,,,
mondo:0004316,acantholytic squamous cell skin carcinoma,"['acantholytic squamous cell skin carcinoma', 'acantholytic squamous cell carcinoma of skin', 'acantholytic squamous cell carcinoma of the skin']",7643,,,C0345979,,C4460,,,,,,
mondo:0004317,multiple spinal canal and spinal cord meningioma,"['multiple spinal canal and spinal cord Meningiomas', 'multiple meningiomas of the spinal canal and spinal cord', 'multiple intraspinal Meningiomas', 'multiple Meningiomas of spinal canal and spinal cord']",7646,,,C1334825,,C5275,,,,,,
mondo:0004318,pulmonary type ovarian small cell carcinoma,"['ovarian small cell carcinoma, pulmonary type']",7650,,,C1518737,,C40440,,,,,,
mondo:0004319,hypercalcemic type ovarian small cell carcinoma,"['SCCOHT', 'ovarian small cell carcinoma, hypercalcemic type']",7651,,,C1518736,,C40439,,,,,,
mondo:0004320,adult infiltrating astrocytic neoplasm,"['adult infiltrating astrocytic neoplasm', 'adult infiltrating astrocytic tumor', 'adult infiltrating astrocytoma', 'adult infiltrating astrocytic tumour']",7656,,,C0281329,,C8289,,,,,,
mondo:0004321,endometrial mixed adenocarcinoma,['endometrial mixed adenocarcinoma'],7664,,,C1516856,,C40153,,,,,,
mondo:0004322,non-gestational ovarian choriocarcinoma,,7665,,,C1518355,,C39991,,,,,,
mondo:0004323,muscular atrophy,"['muscle wasting', 'amyotrophia', 'wasting - muscle']",767,,,,,,,D009133,728.2,,,
mondo:0004324,testicular fibroma,,7675,,,C1515282,,C39951,,,,,,
mondo:0004325,testicular thecoma,"['thecoma of testis', 'testis thecoma']",7676,,,C1515299,,C39952,,,,,,
mondo:0004326,sphenoid sinus inverted papilloma,"['sphenoidal sinus inverted papilloma', 'inverted papilloma of sphenoid sinus', 'inverted papilloma of the sphenoid sinus']",7678,,,C1336037,,C6841,,,,,,
mondo:0004327,sphenoid sinus Schneiderian papilloma,"['Schneiderian papilloma of sphenoid sinus', 'sphenoid sinus Schneiderian papilloma', 'Schneiderian papilloma of the sphenoid sinus']",7679,,,C1336038,,C6838,,,,,,
mondo:0004328,maxillary sinus adenocarcinoma,"['adenocarcinoma of maxillary sinus', 'adenocarcinoma of the maxillary sinus', 'maxillary sinus adenocarcinoma']",7684,,,C1334642,,C6240,,,,,,
mondo:0004329,pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia,"['pancreatic intraductal papillary mucinous neoplasm with high grade dysplasia', 'pancreatic intraductal papillary-mucinous neoplasm with high grade dysplasia', 'pancreatic non-invasive intraductal papillary-mucinous carcinoma']",7685,,,C1518873,,C41251,,,,,,
mondo:0004330,leptomeningeal sarcoma,"['sarcoma of the leptomeninges', 'leptomeninges sarcoma', 'sarcoma of leptomeninx', 'leptomeningeal sarcoma', 'sarcoma of leptomeninges', 'leptomeninx sarcoma', 'sarcoma, meningeal', 'sarcoma, leptomeningeal, malignant']",7689,,,C1384416,,C8312,,,,,,
mondo:0004331,bladder urachal adenocarcinoma,"['urachal adenocarcinoma', 'bladder urachal adenocarcinoma', 'adenocarcinoma of the urachus', 'urachus adenocarcinoma']",7694,,,C1511204,,C39843,,C536474,,,,
mondo:0004332,lung hilum cancer,"['primary malignant neoplasm of hilus of lung', 'malignant lung hilum tumour', 'malignant tumor of lung hilum', 'malignant tumour of the lung hilum', 'malignant hilar lung neoplasm', 'malignant lung hilus neoplasm', 'malignant neoplasm of lung hilus', 'cancer of lung hilus', 'lung hilus cancer', 'malignant lung hilum neoplasm', 'malignant tumor of the lung hilum', 'malignant hilar lung tumour', 'malignant hilar lung tumor', 'malignant neoplasm of lung hilum', 'malignant neoplasm of the lung hilum', 'malignant tumour of lung hilum', 'malignant lung hilum tumor']",7696,,,C2607931,,C4566,,,,,,
mondo:0004333,pancreatic ACTH-producing neuroendocrine tumor,"['pancreatic ACTH producing neuroendocrine tumor', 'pancreatic ACTH hormone producing tumour', 'pancreatic ACTH-producing neuroendocrine tumor', 'pancreatic adrenocorticotropic hormone producing tumor', 'pancreatic ACTH producing neuroendocrine tumour', 'pancreatic adrenocorticotropic hormone producing tumour', 'pancreatic ACTH producing tumour', 'pancreatic ACTH hormone producing tumor', 'pancreatic ACTH producing NET', 'pancreatic ACTH producing tumor']",7697,,,C1335300,,C27466,,,,,,
mondo:0004334,non-functional pancreatic neuroendocrine tumor,"['nonsyndromic pancreatic endocrine tumor', 'non-syndromic pancreatic neuroendocrine tumor', 'non-functioning pancreatic NET', 'nonsyndromic pancreatic neuroendocrine tumour', 'non-functional pancreatic neuroendocrine tumor', 'non-functioning neuroendocrine tumour of pancreas', 'nonsyndromic pancreatic neuroendocrine tumor', 'nonfunctional pancreatic neuroendocrine tumour', 'nonfunctional pancreatic NET', 'inactive pancreatic endocrine tumor', 'non-functioning well-differentiated pancreatic NEN', 'non-functioning pancreatic neuroendocrine tumor', 'non-functioning pancreatic endocrine tumor', 'non-functioning well-differentiated neuroendocrine neoplasm of pancreas', 'non-functioning pancreatic neuroendocrine tumour', 'inactive pancreatic endocrine tumour', 'non functioning pancreatic endocrine tumor', 'non-functioning endocrine pancreatic tumors', 'non functioning pancreatic endocrine tumour', 'non-functioning well differentiated pancreatic endocrine tumour', 'non-functioning well-differentiated NEN of pancreas', 'non-functioning pancreatic endocrine tumour', 'non-functioning EPTs', 'non-functioning endocrine pancreatic tumours', 'non-functioning PNET', 'non-functioning neuroendocrine tumor of pancreas', 'non-syndromic pancreatic NET', 'non-functioning well differentiated pancreatic endocrine tumor', 'non-functioning well-differentiated pancreatic neuroendocrine neoplasm', 'nonfunctional pancreatic neuroendocrine tumor', 'nonsyndromic pancreatic endocrine tumour', 'non-syndromic pancreatic neuroendocrine tumour']",7698,,506075,C1334977,,C45837,1000398,C536126,,,,
mondo:0004335,digestive system disorder,"['digestive disease', 'git disease', 'gastroenterological system disorder', 'digestive system disease', 'gastrointestinal disorder', 'digestive system disorder', 'digestive system disease or disorder', 'gastroenterological system disease', 'gastrointestinal system disease', 'disorder of digestive system', 'gastroenteropathy', 'disease of digestive system', 'gastrointestinal disease', 'stomach or intestinal disorder', 'gastrointestinal system disorder', 'alimentary system disease']",77,,,,,C2990,0000405,D005767,V47.3,K00-K95,,
mondo:0004336,rectal signet ring cell adenocarcinoma,"['signet Ring adenocarcinoma of the rectum', 'signet Ring cell adenocarcinoma of rectum', 'signet Ring cell adenocarcinoma of the rectum', 'signet Ring adenocarcinoma of rectum', 'rectal signet Ring cell adenocarcinoma', 'rectum signet ring cell carcinoma', 'rectum signet ring adenocarcinoma']",7707,,,C0279654,,C9168,,,,,,
mondo:0004337,perianal skin Paget disease,"['anal margin Paget^s disease', 'perianal skin Paget disease', 'Paget^s disease of the anal margin', 'perianal skin Paget^s disease', 'perianal skin mammary Paget^s disease', 'Paget disease of the anal margin']",7708,,,C1332270,,C7476,,,,,,
mondo:0004338,retinal cell cancer,"['cancer of retinal cell', 'malignant neoplasm of retinal cell', 'malignant retinal cell neoplasm', 'retinal cell cancer']",771,,,C1335765,,C7061,,,,,,
mondo:0004339,tuberculum sellae meningioma,"['tuberculum sellae sella turcica neoplasm', 'meningioma of the tuberculum sellae', 'meningioma of tuberculum sellae', 'sella turcica neoplasm of tuberculum sellae']",7713,,,C1336829,,C5284,,,,,,
mondo:0004340,mixed ductal-endocrine carcinoma of pancreas,"['mixed ductal-endocrine carcinoma of the pancreas', 'mixed ductal-endocrine carcinoma', 'mixed ductal-neuroendocrine carcinoma of the pancreas']",7716,,,C1301048,,C6879,,,,,,
mondo:0004341,colloid carcinoma of the pancreas,"['colloid carcinoma of the pancreas', 'mucinous Noncystic carcinoma', 'pancreatic mucinous Noncystic carcinoma']",7717,,,C1333081,,C37214,,,,,,
mondo:0004343,pancreatic acinar cell cystadenocarcinoma,"['acinar cell cystadenocarcinoma', 'acinar cell cystadenocarcinoma of pancreas', 'pancreatic acinar cell cystadenocarcinoma', 'acinar cell cystadenocarcinoma (morphologic abnormality)', 'acinar cell cystadenocarcinoma of the pancreas']",7729,,,C1266087,,C5727,,,,,,
mondo:0004344,childhood malignant hemangiopericytoma,"['malignant childhood hemangiopericytoma', 'malignant pediatric hemangiopericytoma', 'malignant hemangiopericytoma', 'malignant paediatric hemangiopericytoma']",7731,,,C0279983,,C8090,,,,,,
mondo:0004345,childhood malignant schwannoma,"['paediatric malignant neurilemmoma', 'childhood malignant tumor of the peripheral nerve sheath', 'paediatric malignant peripheral nerve sheath tumour', 'paediatric malignant schwannoma', 'childhood neurogenic sarcoma', 'childhood malignant tumour of the peripheral nerve sheath', 'childhood malignant neoplasm of peripheral nerve sheath', 'paediatric malignant tumour of peripheral nerve sheath', 'pediatric malignant neoplasm of peripheral nerve sheath', 'paediatric malignant neoplasm of peripheral nerve sheath', 'childhood malignant schwannoma', 'childhood malignant neoplasm of the peripheral nerve sheath', 'pediatric malignant neoplasm of the peripheral nerve sheath', 'malignant peripheral nerve sheath tumor', 'pediatric malignant tumor of the peripheral nerve sheath', 'pediatric malignant peripheral nerve sheath tumor', 'paediatric malignant tumour of the peripheral nerve sheath', 'childhood malignant neurilemmoma', 'pediatric malignant tumor of peripheral nerve sheath', 'paediatric malignant neoplasm of the peripheral nerve sheath', 'pediatric malignant peripheral nerve sheath neoplasm', 'malignant peripheral nerve sheath tumour', 'paediatric malignant peripheral nerve sheath neoplasm', 'pediatric malignant schwannoma', 'childhood malignant peripheral nerve sheath tumour', 'childhood malignant tumor of peripheral nerve sheath', 'childhood malignant peripheral nerve sheath neoplasm', 'pediatric malignant neurilemmoma', 'childhood malignant peripheral nerve sheath tumor', 'childhood MPNST', 'pediatric MPNST', 'childhood neurofibrosarcoma', 'childhood malignant tumour of peripheral nerve sheath', 'paediatric MPNST']",7732,,,C0279987,,C8094,,,,,,
mondo:0004346,signet ring cell intrahepatic cholangiocarcinoma,['signet Ring cell intrahepatic cholangiocarcinoma'],7733,,,C1519321,,C41619,,,,,,
mondo:0004348,retinal telangiectasia,,7736,,,C0154835,,,,,362.15,,,0007763
mondo:0004349,retina lymphoma,"['retina lymphoma', 'retinal lymphoma', 'lymphoma of the retina', 'lymphoma of retina', 'primary retinal lymphoma']",774,,,C0339556,,C4365,,,198.4,,,
mondo:0004350,pediatric extraocular retinoblastoma,"['pediatric extraocular retinoblastoma', 'childhood metastatic retinoblastoma', 'extraocular retinoblastoma', 'childhood extraocular retinoblastoma', 'extraocular retinoblastoma of childhood']",7747,,,C1321870,,C9048,,,,,,
mondo:0004351,intraocular lymphoma,"['primary intraocular lymphoma', 'PIOL', 'primary intraocular non-Hodgkin^s lymphoma', 'intraocular lymphoma']",775,,279904,,,C9184,,D064090,200.50,,,
mondo:0004352,adult brain ependymoma,"['brain ependymoma', 'adult brain ependymoma']",7750,,,C1332186,,C9372,,,,,,
mondo:0004353,extrahepatic biliary papillomatosis,"['extrahepatic biliary papillomatosis', 'extrahepatic bile duct papillary neoplasm', 'extrahepatic bile duct papillomatosis']",7752,,,C1333511,,C7124,,,,,,
mondo:0004354,neonatal leukemia,['neonatal leukemia'],7756,,,C0235813,,C3845,,,,,,
mondo:0004355,childhood leukemia,"['leukaemia', 'childhood leukemia', 'leukemia', 'leukaemia (disease) of childhood', 'pediatric leukemia (disease)', 'childhood leukaemia (disease)', 'leukemia (disease) of childhood', 'paediatric leukaemia (disease)']",7757,,,C1332977,,C4989,,,,,,
mondo:0004356,childhood multilocular cystic kidney neoplasm,"['pediatric multilocular cystic kidney neoplasm', 'pediatric multilocular cystic renal neoplasm', 'pediatric multilocular cystic renal tumor', 'paediatric multilocular cystic kidney tumour', 'paediatric multilocular cystic renal neoplasm', 'pediatric multilocular cystic kidney tumor', 'childhood multilocular cystic renal tumor', 'childhood multilocular cystic renal neoplasm', 'childhood multilocular cystic kidney tumor', 'paediatric multilocular cystic renal tumour', 'benign multilocular cystic renal tumour', 'benign multilocular cystic renal tumor', 'childhood multilocular cystic renal tumour', 'paediatric multilocular cystic kidney neoplasm', 'childhood multilocular cystic kidney tumour', 'childhood multilocular cystic kidney neoplasm']",7762,,,C1332983,,C6566,,,,,,
mondo:0004357,carcinoma of supraglottis,"['cancer of the supraglottis', 'supraglottic part of larynx carcinoma', 'supraglottic carcinoma', 'carcinoma of supraglottis', 'supraglottic throat cancer', 'cancer of supraglottis', 'carcinoma of supraglottic part of larynx', 'carcinoma of the supraglottis', 'supraglottis carcinoma', 'supraglottic cancer']",7763,,,C1299240,,C5973,,,,,,
mondo:0004358,subglottis carcinoma,"['subglottis carcinoma', 'subglottic carcinoma', 'subglottic cancer', 'carcinoma of subglottis', 'cancer of subglottis', 'cancer of the subglottis', 'carcinoma of the subglottis', 'subglottic throat cancer']",7764,,,C1299239,,C5972,,,,,,
mondo:0004359,delusional disorder,,778,,,,,C94379,,D012563,297.1,,,
mondo:0004360,breast extraskeletal osteosarcoma,"['osteogenic sarcoma of the breast', 'osteogenic sarcoma of breast', 'breast osteosarcoma (disease)', 'osteogenic breast sarcoma', 'osteosarcoma of breast', 'osteosarcoma of the breast', 'breast osteosarcoma', 'breast extraskeletal osteosarcoma']",7787,,,C1335149,,C5189,,,,,,
mondo:0004361,adult spinal cord ependymoma,"['spinal cord ependymoma', 'adult spinal cord ependymoma', 'spinal cord ependymoma of adults']",7788,,,C1332215,,C27399,,,,,,
mondo:0004363,adult spinal cord glioblastoma,"['adult spinal cord glioblastoma', 'adult spinal cord glioblastoma multiforme', 'glioblastoma multiforme of spinal cord']",7806,,,C0559185,,C27183,,,,,,
mondo:0004364,choroid necrotic melanoma,"['necrotic melanoma of choroid', 'necrotic choroid melanoma', 'choroid necrotic melanoma', 'necrotic melanoma of the choroid']",7807,,,C1333026,,C6865,,,,,,
mondo:0004365,necrotic uveal melanoma,,7808,,,C1334931,,C7990,,,,,,
mondo:0004366,mixed astrocytoma-ependymoma-oligodendroglioma,['mixed astrocytoma-ependymoma-oligodendroglioma'],7817,,,C0280792,,C8272,,,,,,
mondo:0004367,petroclival meningioma,,7818,,,C1335395,,C5278,,,,,,
mondo:0004368,sphenoorbital meningioma,,7819,,,C1336040,,C5285,,,,,,
mondo:0004369,renal infectious disease,,782,,,,,,,,590.9,,,
mondo:0004370,sphenocavernous meningioma,,7820,,,C1336036,,C5313,,,,,,
mondo:0004371,spinal multifocal clear cell meningioma,"['spinal multifocal clear cell meningioma', 'multifocal clear cell meningioma of the spine', 'multifocal clear cell meningioma of spine']",7824,,,C1336051,,C5287,,,,,,
mondo:0004372,chronic toxic polyneuropathy,['chronic toxic polyneuropathy'],7825,,,C1333048,,C35603,,,,,,
mondo:0004373,adult papillary meningioma,"['papillary meningioma', 'adult papillary meningioma', 'papillary meningioma of adults']",7826,,,C0281334,,C8293,,,,,,
mondo:0004374,adult extraskeletal osteosarcoma,"['extraosseous osteosarcoma of adults', 'adult extraskeletal osteosarcoma', 'extraskeletal osteosarcoma', 'adult extraosseous osteosarcoma']",7827,,,C0278985,,C7925,,,,,,
mondo:0004375,end stage renal failure,"['end stage renal disease', 'ESRD', 'disease (ESRD), end stage renal', 'renal disease (ESRD), end stage', 'end stage kidney disease', 'chronic kidney disease, stage 5', 'ESRD, end stage renal disease', 'end stage kidney failure', 'renal disease, end stage', 'end stage renal disease (ESRD)']",783,,,,,C9439,,,585.6,N18.5,,
mondo:0004376,infiltrating nipple syringomatous adenoma,"['nipple syringomatous adenoma', 'infiltrating nipple syringomatous adenoma']",7839,,,C1518329,,C40363,,,,,,
mondo:0004377,pancreatic non-functioning delta cell tumor,"['non-functional pancreatic Delta cell NET', 'nonfunctional Pancreatic Delta cell Neuroendocrine tumor', 'non-functioning pancreatic Delta cell tumor', 'non-functional pancreatic Delta cell neuroendocrine tumor', 'non-functional pancreatic Delta cell neuroendocrine tumour', 'nonfunctional Pancreatic Delta cell Neuroendocrine tumour', 'non-functioning pancreatic Delta cell neoplasm', 'non-functioning pancreatic Delta cell tumour']",7840,,,C1335311,,C28333,,,,,,
mondo:0004378,pediatric cerebral ependymoblastoma,"['childhood cerebral embryonal tumor with Multilayered Rosettes, C19MC-altered', 'childhood cerebral ependymoblastoma', 'childhood cerebral embryonal tumour with Multilayered Rosettes, C19MC-altered']",7841,,,C1332962,,C6957,,,,,,
mondo:0004379,female breast carcinoma,"['carcinoma of female breast', 'female breast carcinoma', 'mammary carcinoma of the female breast', 'female breast cancer', 'carcinoma of the female breast', 'mammary carcinoma of female breast', 'breast carcinoma, female']",7843,,,C0007104,,C2918,,,174.9,,,
mondo:0004380,dendritic cell sarcoma,"['follicular dendritic cell sarcoma', 'Dendritic cell sarcoma', 'dendritic cell sarcoma', 'Dendritic cell sarcoma, not otherwise specified (morphologic abnormality)', 'sarcoma of dendritic cell']",7849,,,,,C27260,,,,,,
mondo:0004381,pancreatic intraductal papillary-mucinous neoplasm with low grade dysplasia,"['pancreatic intraductal papillary-mucinous adenoma', 'pancreatic intraductal papillary mucinous neoplasm with Low grade dysplasia', 'pancreatic intraductal papillary-mucinous neoplasm with Low grade dysplasia']",7851,,,C1518868,,C41249,,,,,,
mondo:0004382,laryngeal disorder,"['disorder of larynx', 'larynx disease or disorder', 'laryngeal disorder', 'larynx disease', 'laryngeal disease', 'disease of larynx']",786,,,C0023051,,C26810,,D007818,478.70,,,
mondo:0004383,adult central nervous system germinoma,"['central nervous system germinoma of adults', 'germinoma of the adult CNS', 'central nervous system germinoma', 'germinoma of adult central nervous system', 'adult CNS germinoma', 'germinoma of adult CNS', 'germinoma of the adult central nervous system', 'adult central nervous system germinoma']",7867,,,C1370504,,C5792,,,,,,
mondo:0004384,maxillary sinus inverted papilloma,"['maxillary sinus inverted papilloma', 'inverted papilloma of the maxillary sinus', 'inverted papilloma of maxillary sinus']",7868,,,C1334645,,C6840,,,,,,
mondo:0004385,adult xanthogranuloma,"['adult xanthogranuloma', 'xanthogranuloma of adults']",7875,,,C1332220,,C27514,,,,,,
mondo:0004386,uterine corpus atypical polypoid adenomyoma,"['body of uterus atypical polypoid adenomyoma', 'atypical polypoid adenomyoma of body of uterus']",7878,,,C1519844,,C40235,,,,,,
mondo:0004387,luteoma of pregnancy,"['leuteoma of pregnancy', 'luteoma']",7880,,,C1517842,,C40445,,D018311,,,,
mondo:0004389,mite infestation,,7894,,,C0026229,,,,D008924,133.9,,,
mondo:0004390,ocular hypotension,['hypotony of eye'],790,,,C0028841,,,,D015814,360.30,,,
mondo:0004392,intracranial extraskeletal myxoid chondrosarcoma,"['intracranial chondrosarcoma', 'intracranial extraskeletal myxoid chondrosarcoma']",7903,,,C1334238,,C5462,,,,,,
mondo:0004393,mixed astrocytoma-ependymoma,['mixed astrocytoma-ependymoma'],7907,,,C0280791,,C8271,,,,,,
mondo:0004394,maxillary sinus squamous cell carcinoma,"['maxillary antrum squamous cell carcinoma', 'squamous cell carcinoma of the maxillary sinus', 'maxillary antrum epidermoid carcinoma', 'epidermoid carcinoma of maxillary sinus', 'epidermoid carcinoma of the maxillofacial sinus', 'maxillofacial sinus epidermoid carcinoma', 'squamous cell carcinoma of maxillary sinus', 'maxillary sinus epidermoid carcinoma', 'maxillary sinus squamous cell carcinoma', 'maxillofacial sinus squamous cell carcinoma', 'epidermoid carcinoma of the maxillary antrum', 'epidermoid carcinoma of maxillary antrum', 'squamous cell carcinoma of the maxillofacial sinus', 'squamous cell carcinoma of maxillofacial sinus', 'epidermoid carcinoma of the maxillary sinus', 'squamous cell carcinoma of maxillary antrum', 'squamous cell carcinoma of the maxillary antrum', 'epidermoid carcinoma of maxillofacial sinus']",7910,,,C1334647,,C6064,,,,,,
mondo:0004396,cervical spinal canal and spinal cord meningioma,"['meningioma of cervical spinal canal and spinal cord', 'cervical intraspinal meningioma', 'meningioma of the cervical spinal canal and spinal cord']",7915,,,C1332916,,C5296,,,,,,
mondo:0004397,benign mediastinal psammomatous neurilemmoma,"['benign psammomatous neurilemmoma of mediastinum', 'benign psammomatous schwannoma of the mediastinum', 'benign psammomatous neurilemmoma of the mediastinum', 'benign mediastinal psammomatous schwannoma', 'benign psammomatous schwannoma of mediastinum']",7921,,,C1332513,,C6636,,,,,,
mondo:0004398,mediastinal schwannoma,"['schwannoma of the mediastinum', 'neurilemmoma of the mediastinum', 'schwannoma of mediastinum', 'mediastinal schwannoma', 'benign neurilemmoma of mediastinum', 'benign neurilemmoma of the mediastinum', 'benign mediastinal schwannoma', 'benign schwannoma of the mediastinum', 'benign mediastinal neurilemmoma', 'mediastinum schwannoma', 'benign schwannoma of mediastinum', 'mediastinal neurilemmoma', 'neurilemmoma of mediastinum']",7922,,,C1334679,,C6643,,,,,,
mondo:0004400,malignant type A thymoma,"['malignant type A thymoma', 'thymoma, medullary, malignant']",7927,,,C0279707,,C7999,,,,,,
mondo:0004401,testis refractory cancer,"['refractory malignant testicular germ cell tumour', 'refractory testicular cancer', 'refractory cancer of testis', 'refractory malignant testicular germ cell tumor', 'refractory cancer of the testis', 'refractory testicular carcinoma']",7928,,,C1377904,,C9077,,,,,,
mondo:0004402,"testicular yolk sac tumor, glandular-alveolar pattern","['glandular-alveolar pattern testicular yolk sac tumor', 'testicular yolk sac tumor, glandular-alveolar pattern', 'glandular-alveolar pattern testicular yolk sac tumour']",7930,,,C1515305,,C39926,,,,,,
mondo:0004403,childhood precursor T-lymphoblastic lymphoma/leukemia,"['childhood precursor T-lymphoblastic lymphoma/leukemia', 'precursor T-lymphoblastic lymphoma/leukemia of childhood', 'paediatric precursor T-lymphoblastic lymphoma/leukemia', 'childhood T lymphoblastic leukemia/lymphoma', 'pediatric precursor T-lymphoblastic lymphoma/leukemia']",7933,,,C1332997,,C5640,,,,,,
mondo:0004404,refractory precursor T-lymphoblastic lymphoma/leukemia,"['refractory T lymphoblastic leukemia/lymphoma', 'refractory precursor T-lymphoblastic lymphoma/leukemia', 'precursor T lymphoblastic lymphoma/leukemia refractory']",7936,,,C0854859,,C8696,,,,,,
mondo:0004405,Barrett adenocarcinoma,"['adenocarcinoma arising in Barrett^s mucosa', 'Barrett adenocarcinoma', 'Barrett^s adenocarcinoma']",7941,,,C1332460,,C7027,1001939,,,,,
mondo:0004406,adult central nervous system mixed germ cell tumor,"['adult mixed germ cell tumor of central nervous system', 'central nervous system Mixed germ cell tumor', 'central nervous system Mixed germ cell tumour', 'adult mixed germ cell tumour of central nervous system', 'mixed germ cell tumor of central nervous system of adults', 'mixed germ cell tumour of central nervous system of adults', 'adult central nervous system mixed germ cell tumor']",7945,,,C1332195,,C27402,,,,,,
mondo:0004407,stroma-dominant and stroma-poor composite ganglioneuroblastoma,"['composite ganglioneuroblastoma, Stroma-dominant and Stroma-poor']",7949,,,C1516761,,C42060,,,,,,
mondo:0004408,schwannian stroma-rich and stroma-poor composite ganglioneuroblastoma,"['composite ganglioneuroblastoma, Schwannian Stroma-rich and Stroma-poor']",7951,,,C1516760,,C42059,,,,,,
mondo:0004409,nipple duct carcinoma,['nipple duct carcinoma'],7953,,,C1334967,,C27234,,,,,,
mondo:0004410,sarcomatoid penile squamous cell carcinoma,"['sarcomatoid penile carcinoma', 'sarcomatous carcinoma of the penis', 'sarcomatoid carcinoma of the penis', 'spindle cell carcinoma of the penis', 'sarcomatoid penile squamous cell carcinoma', 'squamous cell carcinoma of the penis, sarcomatoid type', 'squamous cell carcinoma of penis, sarcomatoid type']",7958,,,C1335923,,C6984,,,,,,
mondo:0004411,duodenal gastrin-producing neuroendocrine tumor,"['gastrin producing tumor of duodenum', 'duodenal G-cell gastrin producing tumour', 'duodenal gastrin-producing NET', 'gastrin-producing neuroendocrine tumour of duodenum', 'gastrinoma of the duodenum', 'gastrinoma of duodenum', 'gastrin producing tumor of the duodenum', 'gastrin-producing neuroendocrine tumor of duodenum', 'duodenal gastrin-producing neuroendocrine tumor', 'duodenum gastrin-producing neuroendocrine tumor', 'duodenal G-cell gastrin producing tumor', 'gastrin producing tumour of duodenum', 'duodenal gastrinoma', 'gastrin producing tumour of the duodenum', 'malignant duodenal gastrinoma', 'duodenum gastrin-producing neuroendocrine tumour']",7959,,,C1333321,,C5731,1000224,,,,,
mondo:0004412,malignant spiradenoma,"['malignant eccrine spiradenoma (morphologic abnormality)', 'spiradenoma, malignant', 'Spiradenocarcinoma', 'malignant eccrine spiradenoma', 'malignant spiradenoma']",7960,,,C1266063,,C5117,,,,,,
mondo:0004413,cervical non-keratinizing squamous cell carcinoma,,7961,,,C1518366,,C40188,,,,,,
mondo:0004414,tamoxifen-related endometrial lesion,['tamoxifen-related endometrial disorder'],7962,,,C1515212,,C40159,,,,,,
mondo:0004415,lipid-cell variant infiltrating bladder urothelial carcinoma,"['infiltrating bladder urothelial carcinoma, Lipid-cell variant']",7967,,,C1512738,,C39828,,,,,,
mondo:0004416,plasmacytoid variant infiltrating bladder urothelial carcinoma,"['infiltrating bladder urothelial carcinoma, plasmacytoid variant', 'plasmacytoid/signet ring cell bladder carcinoma']",7968,,,C1512742,,C39823,,,,,,
mondo:0004417,nested variant infiltrating bladder urothelial carcinoma,"['infiltrating bladder urothelial carcinoma, nested variant']",7969,,,C1512741,,C39819,,,,,,
mondo:0004418,microcystic variant infiltrating bladder urothelial carcinoma,"['infiltrating bladder urothelial carcinoma, microcystic variant']",7971,,,C1512740,,C39820,,,,,,
mondo:0004419,lymphoma-like variant infiltrating bladder urothelial carcinoma,"['infiltrating bladder urothelial carcinoma, lymphoma-like variant']",7972,,,C1512739,,C39822,,,,,,
mondo:0004420,breast malignant eccrine spiradenoma,"['malignant spiradenoma of breast', 'breast malignant spiradenoma', 'malignant eccrine spiradenoma of the breast', 'malignant breast eccrine spiradenoma', 'malignant eccrine spiradenoma of breast']",7983,,,C1334565,,C5180,,,,,,
mondo:0004421,sclerosing breast papilloma,"['Complex sclerosing papillary lesion of the breast', 'Complex sclerosing papillary lesion', 'sclerosing breast papilloma']",7984,,,C1335932,,C27944,,,,,,
mondo:0004422,cerebral falx meningioma,"['meningioma of falx cerebri', 'falx cerebri meningioma (disease)', 'meningioma of falx of cerebrum', 'Falcine meningioma', 'meningioma of the falx of the cerebrum', 'falx cerebri meningioma', 'meningioma of cerebral falx', 'meningioma of the falx cerebri', 'meningioma of the cerebral falx']",7986,,,C1333597,,C5267,,,,,,
mondo:0004423,central nervous system extraskeletal osteosarcoma,"['central nervous system osteosarcoma (disease)', 'osteosarcoma of central nervous system', 'osteosarcoma of the central nervous system', 'central nervous system osteosarcoma', 'central nervous system extraskeletal osteosarcoma']",7994,,,C1335150,,C7002,,,,,,
mondo:0004425,hyperthyroidism,['overactive thyroid'],7998,,,,,C3123,0009189,D006980,242.90,,,
mondo:0004426,frontal convexity meningioma,,8000,,,C1333643,,C5292,,,,,,
mondo:0004427,supraglottis neoplasm,"['supraglottic part of larynx tumor', 'tumour of the supraglottis', 'neoplasm of supraglottic part of larynx', 'supraglottic tumour', 'neoplasm of supraglottis', 'supraglottis neoplasm', 'supraglottic tumor', 'supraglottic neoplasm', 'supraglottis tumour', 'tumor of supraglottic part of larynx', 'tumour of supraglottis', 'supraglottic part of larynx neoplasm (disease)', 'tumor of the supraglottis', 'neoplasm of the supraglottis', 'supraglottis tumor', 'supraglottic part of larynx tumour', 'tumour of supraglottic part of larynx', 'tumor of supraglottis']",8002,,,C0345726,,C6793,,,,,,
mondo:0004428,alveoli adenoma,"['adenoma, bronchioloalveolar, benign', 'alveolar adenoma', 'adenoma of the alveoli', 'alveolar adenoma (morphologic abnormality)', 'adenoma of alveoli']",8003,,,C0334303,,C4140,,,,,,
mondo:0004429,skin meningioma,"['zone of skin meningioma (disease)', 'primary meningioma of the skin']",8006,,,C1335481,,,,,,,,
mondo:0004430,penis mixed squamous cell carcinoma,['mixed squamous cell carcinoma of the penis'],8009,,,C1513369,,C39959,,,,,,
mondo:0004431,hemarthrosis,"['hemarthrosis of the pelvic region and thigh', 'hemarthrosis of forearm', 'hemarthrosis of the upper arm', 'haemarthrosis of the pelvic region and thigh', 'hemarthrosis involving ankle and foot', 'hemarthrosis of the ankle and foot', 'hemarthrosis of the shoulder region', 'hemarthrosis of the lower leg', 'hemarthrosis of shoulder', 'hemarthrosis of the forearm', 'hemarthrosis of lower leg', 'hemarthrosis involving forearm', 'hemarthrosis of the ankle and/or foot', 'hemarthrosis involving lower leg', 'hemarthrosis of shoulder region', 'hemarthrosis of upper arm', 'haemarthrosis of shoulder joint', 'hemarthrosis involving upper arm', 'hemarthrosis of ankle and/or foot', 'hemarthrosis of the hand', 'haemarthrosis of the ankle and foot', 'hemarthrosis of hand', 'hemarthrosis involving shoulder region', 'hemarthrosis involving pelvic region and thigh', 'hemarthrosis involving hand']",801,,,C0158159,,,1001344,D006395,719.18,,,
mondo:0004432,mature pericardial teratoma,"['benign pericardial teratoma', 'mature pericardial teratoma', 'mature teratoma of the pericardium', 'mature teratoma of pericardium', 'pericardium mature teratoma']",8012,,,C1334638,,C6744,,,,,,
mondo:0004433,papillary carcinoma of the penis,"['papillary carcinoma of penis', 'papillary squamous carcinoma of penis', 'squamous carcinoma of penis, papillary type', 'papillary carcinoma of the penis', 'papillary squamous carcinoma of the penis', 'squamous carcinoma of the penis, papillary type', 'papillary penile carcinoma', 'papillary penile squamous carcinoma', 'penis papillary carcinoma']",8013,,,C1335322,,C6983,,,,,,
mondo:0004435,liver fibrosarcoma,"['hepatic fibrosarcoma', 'liver fibrosarcoma', 'fibrosarcoma of liver', 'fibrosarcoma of the liver', 'liver fibrosarcoma (disease)']",8022,,,C1333966,,C5832,,,,,,
mondo:0004436,ovarian myxoid liposarcoma,"['myxoid liposarcoma of ovary', 'ovarian myxoid liposarcoma', 'ovary myxoid liposarcoma', 'myxoid liposarcoma of the ovary']",8023,,,C1335170,,C5235,,,,,,
mondo:0004438,sporadic breast cancer,"['sporadic breast cancer', 'sporadic breast carcinoma']",8029,,,C1336076,,C7566,,,,,,
mondo:0004439,periocular meningioma,,8030,,,C1335383,,C6777,,,,,,
mondo:0004440,pineal region meningioma,"['meningioma of the pineal gland', 'pineal meningioma', 'pineal body meningioma (disease)', 'meningioma of pineal region', 'meningioma of pineal gland', 'pineal area meningioma', 'pineal gland meningioma', 'meningioma of pineal area', 'meningioma of the pineal area', 'meningioma of the pineal region']",8031,,,C1335418,,C6756,,,,,,
mondo:0004441,childhood ovarian embryonal carcinoma,"['pediatric embryonal carcinoma of the ovary', 'paediatric embryonal carcinoma of ovary', 'ovarian embryonal carcinoma of childhood', 'pediatric ovarian embryonal carcinoma', 'childhood embryonal carcinoma of ovary', 'childhood embryonal carcinoma of the ovary', 'paediatric embryonal carcinoma of the ovary', 'paediatric ovarian embryonal carcinoma', 'pediatric embryonal carcinoma of ovary']",8036,,,C1332989,,C6546,,,,,,
mondo:0004442,testis polyembryoma,"['polyembryoma of testis', 'polyembryoma of the testis', 'testicular polyembryoma']",8042,,,C1514200,,C40962,,,,,,
mondo:0004443,chest wall parachordoma,"['parachordoma of the chest wall', 'parachordoma of chest wall', 'chest wall parachordoma']",8043,,,C1332934,,C6720,,,,,,
mondo:0004444,bladder tubulo-cystic clear cell adenocarcinoma,['bladder tubulo-cystic clear cell adenocarcinoma'],8050,,,C1511203,,C39847,,,,,,
mondo:0004445,bladder papillary clear cell adenocarcinoma,['bladder papillary clear cell adenocarcinoma'],8051,,,C1511196,,C39848,,,,,,
mondo:0004446,olfactory groove meningioma,"['olfactory sulcus meningioma (disease)', 'meningioma of the olfactory groove', 'meningioma of olfactory groove']",8057,,,C1335107,,C6771,,,,,,
mondo:0004447,pituitary stalk meningioma,"['meningioma of the pituitary stalk', 'meningioma of pituitary stalk', 'pituitary stalk meningioma (disease)']",8058,,,C1335422,,C5311,,,,,,
mondo:0004448,frontal sinus inverted papilloma,"['inverted papilloma of frontal sinus', 'inverted papilloma of the frontal sinus', 'frontal sinus inverted papilloma']",8060,,,C1333644,,C6842,,,,,,
mondo:0004449,intraductal breast myoepitheliosis,,8068,,,C1512935,,C40387,,,,,,
mondo:0004450,carotid artery occlusion,"['carotid artery segment occlusion precerebral artery', 'occlusion precerebral artery of carotid artery segment', 'occlusion and stenosis of carotid artery']",807,,,C0265101,,,,,433.10,,,
mondo:0004451,sarcomatous intrahepatic cholangiocarcinoma,"['intrahepatic cholangiocarcinoma with extensive sarcomatous changes', 'sarcomatoid intrahepatic cholangiocarcinoma']",8072,,,C1519184,,C41620,,,,,,
mondo:0004452,childhood central nervous system germinoma,"['central nervous system germinoma of childhood', 'Central nervous system germinoma', 'pediatric central nervous system germinoma', 'paediatric central nervous system germinoma']",8078,,,C1332953,,C27406,,,,,,
mondo:0004453,"testicular yolk sac tumor, myxomatous pattern","['myxomatous pattern testicular yolk sac tumour', 'testicular yolk sac tumor, myxomatous pattern', 'myxomatous pattern testicular yolk sac tumor']",8081,,,C1515309,,C39929,,,,,,
mondo:0004454,cellular congenital mesoblastic nephroma,['cellular congenital mesoblastic nephroma'],8082,,,C1516474,,C39815,,,,,,
mondo:0004455,classic congenital mesoblastic nephroma,['classic congenital mesoblastic nephroma'],8083,,,C1516475,,C39814,,,,,,
mondo:0004456,cocaine abuse,,809,,,,,,,,305.60,,,
mondo:0004457,maxillary sinus Schneiderian papilloma,"['maxillary sinus Schneiderian papilloma', 'maxillary sinus paranasal sinus Schneiderian papilloma', 'Schneiderian papilloma of the maxillary sinus', 'Schneiderian papilloma of maxillary sinus', 'paranasal sinus Schneiderian papilloma of maxillary sinus']",8093,,,C1334646,,C6839,,,,,,
mondo:0004458,bladder mixed adenocarcinoma,,8096,,,C1511192,,C39839,,,,,,
mondo:0004459,bladder hepatoid adenocarcinoma,['bladder hepatoid adenocarcinoma'],8097,,,C1511189,,C39838,,,,,,
mondo:0004460,thyroid gland fetal adenoma,"['microfollicular adenoma', 'foetal adenoma', 'microfollicular adenoma (morphologic abnormality)', 'thyroid gland microfollicular adenoma', 'thyroid foetal adenoma', 'thyroid fetal adenoma']",8102,,,C0334328,,C4160,,,,,,
mondo:0004461,vaginal tubulovillous adenoma,['vaginal tubulovillous adenoma'],8104,,,C1519933,,C40258,,,,,,
mondo:0004462,extrahepatic bile duct cystadenoma,"['cystadenoma of the extrahepatic bile duct', 'extrahepatic bile duct mucinous cystic neoplasm', 'extrahepatic bile duct cystadenoma', 'cystadenoma of extrahepatic bile duct']",8105,,,C1333504,,C5851,,,,,,
mondo:0004463,cellular phase chronic idiopathic myelofibrosis,"['primary myelofibrosis, Prefibrotic/early stage', 'Prefibrotic/Early Primary myelofibrosis', 'primary myelofibrosis, Prefibrotic stage', 'chronic idiopathic myelofibrosis, Prefibrotic stage', 'chronic idiopathic myelofibrosis, cellular phase', 'PMFPES']",8106,,,C1516553,,C41237,,,,,,
mondo:0004464,nephrogenic adenoma of the urethra,"['nephrogenic adenoma of urethra', 'urethral nephrogenic adenoma', 'urethra nephrogenic adenoma']",8109,,,C1336889,,C7416,,,,,,
mondo:0004465,periampullary adenocarcinoma,"['periampullary cancer', 'periampullary region of duodenum adenocarcinoma', 'periampullary adenocarcinoma']",8110,,,C1335377,,C27322,,,,,,
mondo:0004466,neuronitis,['neuroinflammation'],8117,,,C0027881,,C34847,,,,,,
mondo:0004467,mature gastric teratoma,"['stomach mature teratoma', 'mature teratoma of the stomach', 'mature teratoma of stomach', 'mature gastric teratoma']",8118,,,C1334635,,C5260,,,,,,
mondo:0004468,anal canal Paget disease,"['anal canal Paget disease', 'anal canal mammary Paget^s disease', 'Paget^s disease of the anal canal', 'anal canal Paget^s disease', 'Paget^s disease of anal canal', 'Paget disease of the anal canal']",8119,,,C1332261,,C7477,,,,,,
mondo:0004469,pseudovascular skin squamous cell carcinoma,"['skin pseudovascular squamous cell carcinoma', 'pseudovascular skin squamous cell carcinoma']",8122,,,C1335974,,C27542,,,,,,
mondo:0004471,bacterial arthritis,"['pyogenic arthritis', 'infectious arthritis', 'septic arthritis']",813,,,,,C26700,1001351,D001170,711.97,,,
mondo:0004472,breast columnar cell mucinous carcinoma,['breast columnar cell mucinous carcinoma'],8130,,,C1511305,,C40355,,,,,,
mondo:0004473,epiglottis cancer,"['malignant neoplasm of the Epiglottis', 'cancer of epiglottis', 'epiglottic throat cancer', 'malignant Epiglottis tumour', 'epiglottic carcinoma', 'malignant epiglottic tumor', 'malignant epiglottis neoplasm', 'epiglottis cancer', 'malignant Epiglottis neoplasm', 'malignant neoplasm of anterior aspect of epiglottis', 'malignant neoplasm of Epiglottis', 'malignant Epiglottis tumor', 'malignant epiglottic tumour', 'malignant neoplasm of anterior epiglottis', 'malignant tumour of Epiglottis', 'malignant neoplasm of anterior surface of epiglottis', 'malignant tumour of the Epiglottis', 'malignant tumor of Epiglottis', 'malignant neoplasm of epiglottis', 'malignant tumor of the Epiglottis', 'epiglottic cancer', 'malignant epiglottic neoplasm']",8133,,,,,C4836,,,146.4,C10.1,,
mondo:0004474,gallbladder lymphoma,"['gallbladder lymphoma', 'gall bladder lymphoma', 'lymphoma of gallbladder', 'lymphoma of the gallbladder', 'primary gallbladder lymphoma', 'lymphoma of gall bladder']",8135,,,C1333748,,C5734,,,,,,
mondo:0004475,thymus clear cell carcinoma,"['clear cell carcinoma of Thymus', 'Thymus clear cell carcinoma', 'clear cell carcinoma of the Thymus', 'thymus clear cell carcinoma', 'thymic clear cell carcinoma']",8137,,,C1333069,,C6462,,,,,,
mondo:0004477,adrenal gland ganglioneuroblastoma,"['adrenal gland ganglioneuroblastoma', 'adrenal gland ganglioneuroblastoma (disease)', 'adrenal ganglioneuroblastoma']",8140,,,C1332176,,C7646,,,,,,
mondo:0004478,pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma,"['CLL/SLL with unmutated IGVH', 'chronic lymphocytic leukemia/small lymphocytic lymphoma with unmutated Immunoglobulin heavy chain variable-region Gene', 'pregerminal center chronic lymphocytic leukemia/small lymphocytic lymphoma']",8144,,,C1333038,,C37204,,,,,,
mondo:0004479,malignant childhood germ cell neoplasm,"['malignant childhood germ cell neoplasm', 'malignant paediatric germ cell neoplasm', 'malignant paediatric germ cell tumour', 'malignant childhood germ cell tumor', 'malignant pediatric germ cell neoplasm', 'malignant childhood germ cell tumour', 'malignant pediatric germ cell tumor']",8149,,,C1334574,,C6541,,,,,,
mondo:0004481,pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma,"['pancreatic intraductal papillary-mucinous neoplasm with an associated invasive carcinoma', 'pancreatic intraductal papillary mucinous neoplasm with an associated invasive carcinoma', 'pancreatic invasive intraductal papillary-mucinous carcinoma']",8150,,,C3274138,,C5726,,,,,,
mondo:0004482,fibroosseous pseudotumor of the digits,"['fibroosseous digital pseudotumor', 'fibroosseous pseudotumor of the digits', 'fibroosseous pseudotumor of digits']",8153,,,C1333612,,C6573,,,215.9,,,
mondo:0004483,thyroid gland oncocytic adenoma,"['benign oncocytoma of the thyroid gland', 'oncocytic adenoma of the thyroid', 'Hurthle cell adenoma of thyroid', 'Hurthle cell adenoma of the thyroid', 'thyroid gland Hurthle cell adenoma', 'benign oncocytoma of thyroid', 'benign oncocytoma of the thyroid', 'thyroid gland oncocytic adenoma', 'follicular adenoma of the thyroid of the oxyphilic cell type', 'oncocytic adenoma of thyroid', 'Hurthle cell adenoma of the thyroid gland', 'thyroid gland follicular adenoma of the oxyphilic cell type', 'benign thyroid oncocytoma', 'benign thyroid gland oncocytoma', 'follicular adenoma of thyroid gland of oxyphilic cell type', 'thyroid follicular adenoma of the oxyphilic cell type', 'Hurthle cell adenoma of thyroid gland', 'thyroid Hurthle cell adenoma', 'thyroid oncocytic adenoma', 'oncocytic adenoma of the thyroid gland', 'follicular adenoma of the thyroid gland of the oxyphilic cell type', 'OAT', 'benign oncocytoma of thyroid gland', 'Hurthle cell adenoma', 'follicular adenoma of thyroid of oxyphilic cell type', 'thyroid follicular adenoma of oxyphilic cell type', 'oncocytic adenoma of thyroid gland', 'thyroid gland follicular adenoma of oxyphilic cell type']",8162,,,C1336750,,C6042,,,,,,
mondo:0004484,gallbladder melanoma,"['melanoma of gallbladder', 'gall bladder melanoma (disease)', 'gallbladder melanoma', 'gallbladder malignant melanoma', 'malignant melanoma of gallbladder', 'melanoma of the gallbladder', 'malignant melanoma of the gallbladder']",8167,,,C1333749,,C5735,,,,,,
mondo:0004485,interstitial myocarditis,,817,,,C0027060,,C35786,,,,,,
mondo:0004486,endocervical type cervical adenomyoma,"['cervical adenomyoma, endocervical type']",8177,,,C1516405,,C40232,,,,,,
mondo:0004487,endometrial type cervical adenomyoma,"['cervical adenomyoma, endometrial type']",8178,,,C1516406,,C40233,,,,,,
mondo:0004488,cervical atypical polypoid adenomyoma,,8179,,,C1516409,,C40234,,,,,,
mondo:0004489,fallopian tube gestational choriocarcinoma,"['fallopian tube gestational choriocarcinoma', 'gestational choriocarcinoma of fallopian tube', 'gestational choriocarcinoma of the fallopian tube']",8186,,,C1333593,,C6278,,,,,,
mondo:0004490,gestational uterine corpus choriocarcinoma,"['gestational choriocarcinoma of body of uterus', 'body of uterus gestational choriocarcinoma']",8187,,,,,,,,,,,
mondo:0004491,uterine corpus choriocarcinoma,"['body of uterus choriocarcinoma (disease)', 'gestational uterine corpus choriocarcinoma', 'uterine corpus gestational choriocarcinoma', 'choriocarcinoma']",8188,,,C1336904,,C27246,,,,,,
mondo:0004492,mediastinitis,,819,,,C0025064,,C26827,,D008480,519.2,J98.51,,
mondo:0004493,"testicular yolk sac tumor, papillary pattern","['papillary pattern testicular yolk sac tumor', 'papillary pattern testicular yolk sac tumour', 'testicular yolk sac tumor, papillary pattern']",8193,,,C1515310,,C39928,,,,,,
mondo:0004494,"testicular yolk sac tumor, hepatoid pattern","['testicular yolk sac tumor, hepatoid pattern', 'hepatoid pattern testicular yolk sac tumor', 'hepatoid pattern testicular yolk sac tumour']",8195,,,C1515306,,C39931,,,,,,
mondo:0004495,myotonic cataract,,82,,,C0027128,,C34833,,,366.43,,,
mondo:0004496,myocarditis,"['myocardial inflammation', 'myocardium inflammation', 'myocardial inflammation (finding)']",820,,,C0027059,,C34831,,D009205,429.0,I40,,
mondo:0004497,tertiary syphilis,['late syphilis'],8200,,,C0153188,,C128414,,C536774,097.0,,,
mondo:0004498,sacral spinal canal and spinal cord meningioma,"['sacral intraspinal meningioma', 'meningioma of sacral spinal canal and spinal cord', 'meningioma of the sacral spinal canal and spinal cord']",8203,,,C1335893,,C5299,,,,,,
mondo:0004499,lung hilum carcinoma,"['lung hilus carcinoma', 'lung hilum cancer', 'hilar lung carcinoma', 'lung hilum carcinoma', 'carcinoma of lung hilus']",8207,,,C1334445,,C7454,,,,,,
mondo:0004500,lung superior sulcus carcinoma,"['superior sulcus lung carcinoma', 'superior sulcus carcinoma of the lung', 'superior sulcus carcinoma of lung']",8208,,,C1336529,,C7779,,,,,,
mondo:0004501,fallopian tube cystadenofibroma,"['fallopian tube serous cystadenofibroma', 'cystadenofibroma of fallopian tube', 'fallopian tube cystadenofibroma']",8211,,,C1517111,,C40114,,,,,,
mondo:0004502,parapharyngeal meningioma,,8216,,,C1335345,,C5303,,,,,,
mondo:0004503,upper clivus meningioma,"['meningioma of upper clivus', 'meningioma of the upper clivus']",8221,,,C1336871,,C5290,,,,,,
mondo:0004504,penile urethral cancer,"['urethra cancer of penis', 'penile urethral malignant neoplasm', 'penis urethra cancer']",8223,,,C1518950,,C39868,,,,,,
mondo:0004505,central breast papilloma,"['solitary intraductal breast papilloma', 'large duct breast papilloma']",8224,,,C1332896,,C36087,,,,,,
mondo:0004506,microscopic breast papilloma,"['microscopic breast papilloma', 'peripheral breast papilloma']",8225,,,C1335390,,C36088,,,,,,
mondo:0004507,atypical breast papilloma,['atypical breast papilloma'],8227,,,C1332346,,C36089,,,,,,
mondo:0004508,periapical periodontitis,['apical periodontitis'],823,,,C0031030,,,1001391,D010485,,,,
mondo:0004509,intrahepatic biliary papillomatosis,"['intrahepatic bile duct papillomatosis', 'intrahepatic bile duct papillary neoplasm', 'intrahepatic biliary papillomatosis']",8230,,,C1334258,,C7125,,,,,,
mondo:0004510,inflammatory liposarcoma,['inflammatory liposarcoma'],8233,,,C1370890,,C6508,,,,,,
mondo:0004511,lower clivus meningioma,"['meningioma of Lower clivus', 'meningioma of the lower clivus']",8239,,,C1334434,,C5288,,,,,,
mondo:0004512,meningeal melanomatosis,"['meningeal melanomatosis', 'meningeal melanomatosis (morphologic abnormality)', 'leptomeningeal melanomatosis', 'melanomatosis of meningeal cluster', 'meningeal cluster melanomatosis']",8243,,,C1266114,,C6891,,,,,,
mondo:0004513,adult pleomorphic rhabdomyosarcoma,"['adult pleomorphic rhabdomyosarcoma', 'pleomorphic rhabdomyosarcoma of adults']",8251,,,C1332211,,C27369,,,,,,
mondo:0004514,chronic rhinitis,"['rhinitis - chronic', 'rhinitis, chronic']",8252,,,C0008711,,C34479,,,472.0,,,
mondo:0004516,bulbomembranous urethral cancer,['bulbomembranous urethral malignant neoplasm'],8259,,,C1511339,,C39869,,,,,,
mondo:0004517,ureter tuberculosis,"['ureter tuberculosis', 'tuberculosis of ureter']",827,,,C0152800,,,,,016.20,,,
mondo:0004518,anterior urethra cancer,"['anterior urethral malignant tumour', 'anterior urethra malignant tumour', 'anterior urethral malignant tumor', 'malignant tumor of the anterior urethra', 'anterior urethra malignant neoplasm', 'malignant tumour of anterior urethra', 'malignant tumour of the anterior urethra', 'malignant tumor of anterior urethra', 'malignant neoplasm of anterior urethra', 'anterior urethral cancer', 'malignant neoplasm of the anterior urethra', 'anterior urethra malignant tumor', 'anterior urethral malignant neoplasm']",8272,,,C0279930,,C7641,,,,,,
mondo:0004519,synovial angioma,"['hemangioma of the synovium', 'hemangioma of synovium', 'synovial hemangioma', 'hemangioma of layer of synovial tissue', 'angioma of the synovium', 'angioma of synovium', 'layer of synovial tissue hemangioma']",8274,,,C1336546,,C6525,,,,,,
mondo:0004520,intratubular embryonal carcinoma,"['intratubular embryonal carcinoma', 'stage 0 testicular embryonal carcinoma', 'stage 0 testicular embryonal carcinoma aJCC v7', 'stage 0 testicular embryonal carcinoma aJCC v6 and v7', 'stage 0 testicular embryonal carcinoma aJCC v6']",8275,,,C1336096,,C7325,,,,,,
mondo:0004521,adult epithelioid sarcoma,"['epithelioid sarcoma of adults', 'adult epithelioid sarcoma', 'epithelioid sarcoma']",8282,,,C0279545,,C7944,,,,,,
mondo:0004522,peritonitis,"['primary bacterial peritonitis', 'peritoneum inflammation', 'acute generalized peritonitis', 'retractile mesenteritis', 'acute generalised peritonitis']",8283,,,,,C26849,0008588,D010538,567.89,,,
mondo:0004523,clear cell squamous cell skin carcinoma,"['clear cell squamous cell carcinoma of skin', 'clear cell squamous cell skin carcinoma', 'clear cell squamous cell carcinoma of the skin']",8288,,,C0345978,,C4459,,,,,,
mondo:0004524,thyroid gland atypical follicular adenoma,"['atypical follicular adenoma (morphologic abnormality)', 'thyroid gland atypical follicular adenoma', 'atypical follicular adenoma']",8292,,,C1266046,,C27729,,,,,,
mondo:0004525,scabies,"['Sarcoptes scabiei caused disease or disorder', 'infestation by Sarcoptes scabiei var hominis', 'sarcoptic itch', 'infestation by Sarcoptes scabiei']",8295,,,C0036262,,C34998,,D012532,133.0,B86,,
mondo:0004526,mixed endometrial stromal and smooth muscle tumor,"['Stromomyoma', 'mixed endometrial stromal and smooth muscle neoplasm', 'uterine corpus soft tissue neoplasm']",8302,,,C1519865,,C40178,,,,,,
mondo:0004527,congenital granular cell tumor,['congenital granular cell tumor'],8303,,,,,,,,,,,
mondo:0004528,lymph node palisaded myofibroblastoma,"['palisaded lymph node myofibroblastoma', 'palisaded myofibroblastoma of the lymph node', 'palisaded myofibroblastoma of lymph node']",8304,,,C1335295,,C6584,,,,,,
mondo:0004529,non-ossifying fibromyxoid tumor,"['nonossifying fibromyxoma', 'nonossifying fibromyxoid tumour', 'nonossifying fibromyxoid neoplasm', 'nonossifying fibromyxoid tumor']",8305,,,C1335063,,C6583,,,,,,
mondo:0004530,early invasive cervical adenocarcinoma,['cervical microinvasive adenocarcinoma'],8307,,,C1333369,,C36096,,,,,,
mondo:0004531,sclerosing adenosis of breast,"['sclerosing adenosis of the breast', 'breast sclerosing adenosis', 'sclerosing breast adenosis', 'sclerosing adenosis']",8310,,,C1335931,,C5205,,,,,,
mondo:0004532,auditory system cancer,"['malignant auditory system neoplasm', 'auditory system cancer', 'cancer of auditory system', 'malignant neoplasm of auditory system']",833,,,,,C3000,,D004428,,,,
mondo:0004533,perineural angioma,['perineural hemangioma'],8331,,,C1335382,,C6526,,,,,,
mondo:0004534,microglandular adenosis of breast,"['breast microglandular adenosis', 'microglandular adenosis of the breast']",8335,,,C1334753,,C5199,,,,,,
mondo:0004535,childhood choriocarcinoma of the ovary,"['pediatric ovarian choriocarcinoma', 'paediatric ovarian choriocarcinoma', 'choriocarcinoma of ovary of childhood', 'pediatric choriocarcinoma of the ovary', 'paediatric choriocarcinoma of ovary', 'childhood choriocarcinoma of ovary', 'childhood ovarian choriocarcinoma', 'paediatric choriocarcinoma of the ovary', 'pediatric choriocarcinoma of ovary']",8336,,,C1332987,,C6549,,,,,,
mondo:0004537,intestinal variant cervical mucinous adenocarcinoma,"['cervical mucinous adenocarcinoma, intestinal variant', 'intestinal type mucinous carcinoma', 'cervical mucinous adenocarcinoma, intestinal-type']",8339,,,C1516422,,C40203,,,,,,
mondo:0004538,endocervical type cervical mucinous adenocarcinoma,"['cervical mucinous adenocarcinoma, endocervical type', 'cervical adenocarcinoma, endocervical type']",8340,,,C1516421,,C40202,,,,,,
mondo:0004539,aortic malignant tumor,"['malignant aortic neoplasm', 'malignant tumor of the aorta', 'aortic malignant neoplasm', 'malignant tumor of aorta', 'malignant tumour of the aorta', 'malignant aorta neoplasm', 'cancer of aorta', 'malignant neoplasm of aorta', 'malignant neoplasm of the aorta', 'malignant tumour of aorta']",8352,,,C1334560,,C5375,,,,,,
mondo:0004540,epithelioid malignant peripheral nerve sheath tumor,"['malignant epithelioid peripheral nerve sheath tumour', 'malignant epithelioid neoplasm of peripheral nerve sheath', 'malignant epithelioid neoplasm of the peripheral nerve sheath', 'malignant epithelioid tumor of the peripheral nerve sheath', 'epithelioid MPNST', 'malignant epithelioid tumor of peripheral nerve sheath', 'malignant epithelioid peripheral nerve sheath neoplasm', 'malignant epithelioid tumour of peripheral nerve sheath', 'epithelioid malignant peripheral nerve sheath tumor', 'malignant epithelioid peripheral nerve sheath tumor', 'malignant epithelioid tumour of the peripheral nerve sheath']",8353,,,C1321427,,C6561,1000245,,,,,
mondo:0004541,pseudoglandular variant testicular seminoma,"['testicular seminoma, pseudoglandular variant']",8358,,,C1515293,,C40958,,,,,,
mondo:0004542,"cervical adenosquamous carcinoma, glassy cell variant","['glassy cell carcinoma of the cervix uteri', 'glassy cell carcinoma of the cervix', 'glassy cell adenocarcinoma of the uterine cervix', 'glassy cell variant cervical adenosquamous carcinoma', 'GCC of the cervix', 'cervical adenosquamous carcinoma, glassy cell variant']",8361,,213833,,,C40212,,C536823,,C53.0,,
mondo:0004543,enteric pattern testicular yolk sac tumor,"['testicular yolk Sac tumor, enteric pattern']",8362,,,C1515304,,C39932,,,,,,
mondo:0004544,chordoid meningioma,"['meningioma, chordoid', 'chordoid meningioma', 'CHOM', 'meningioma, chordoid (morphologic abnormality)']",8368,,,C1370510,,C6908,1000176,,,,,
mondo:0004545,adult malignant schwannoma,"['adult malignant peripheral nerve sheath neoplasm', 'adult MPNST', 'adult malignant tumour of the peripheral nerve sheath', 'adult malignant neoplasm of the peripheral nerve sheath', 'adult malignant neurilemmoma', 'adult malignant neoplasm of peripheral nerve sheath', 'adult malignant peripheral nerve sheath tumour', 'adult malignant tumor of the peripheral nerve sheath', 'adult malignant tumour of peripheral nerve sheath', 'malignant peripheral nerve sheath tumor', 'malignant peripheral nerve sheath tumour', 'adult malignant peripheral nerve sheath tumor', 'adult malignant tumor of peripheral nerve sheath', 'adult malignant schwannoma']",8369,,,C0278622,,C7814,,,,,,
mondo:0004546,lumbar plexus neoplasm,"['tumour of lumbar plexus', 'neoplasm of lumbar plexus', 'tumor of lumbar nerve plexus', 'neoplasm of the lumbar plexus', 'lumbar nerve plexus tumour', 'lumbar nerve plexus neoplasm (disease)', 'neoplasm of lumbar nerve plexus', 'lumbar plexus neoplasms', 'tumour of lumbar nerve plexus', 'lumbar nerve plexus tumor', 'tumor of the lumbar plexus', 'lumbar plexus tumor', 'lumbar plexus tumour', 'tumour of the lumbar plexus', 'tumor of lumbar plexus']",8389,,,C1334437,,C5824,,,,,,
mondo:0004547,reticular pattern testicular yolk sac tumor,"['testicular yolk Sac tumor, microcystic pattern', 'testicular yolk Sac tumor, reticular pattern']",8392,,,C1515308,,C39923,,,,,,
mondo:0004548,adult type testicular granulosa cell tumor,"['adult testicular granulosa cell tumour', 'adult type testicular granulosa cell tumor']",8394,,,C1515284,,C39946,,,,,,
mondo:0004549,cork-handlers^ disease,"['cork-handlers^ disease or lung', 'cork worker^s lung', 'cork-handlers^ lung', 'cork workers lung', 'Suberosis']",840,,,C0152108,,,,,495.3,,,
mondo:0004550,malignant cornea melanoma,"['melanoma of cornea', 'melanoma of the cornea', 'corneal melanoma', 'malignant corneal melanoma', 'malignant cornea melanoma', 'malignant melanoma of cornea', 'cornea melanoma', 'malignant melanoma of the cornea', 'cornea melanoma (disease)']",8400,,,C0346367,,C4553,,,,,,
mondo:0004551,Meckel diverticulitis,"['Meckel^s diverticulum inflammation', 'Meckel diverticulitis', 'Meckel^s diverticulitis']",8408,,,C0267497,,C27300,,,,,,
mondo:0004552,microinvasive cervical squamous cell carcinoma,['early invasive cervical squamous cell carcinoma'],8409,,,C1333370,,C36094,,,,,,
mondo:0004554,childhood kidney angiomyolipoma,"['pediatric renal angiomyolipoma', 'paediatric kidney angiomyolipoma', 'childhood renal angiomyolipoma', 'kidney angiomyolipoma of childhood', 'paediatric renal angiomyolipoma', 'pediatric kidney angiomyolipoma']",8410,,,C1333000,,C6565,,,,,,
mondo:0004555,kidney angiomyolipoma,"['kidney angiomyolipoma', 'RAML', 'renal angiomyolipoma', 'angiomyolipoma of the kidney', 'angiomyolipoma of kidney']",8411,,,C0241961,,C3888,1000312,,,,,
mondo:0004556,carcinoma arising in nasal papillomatosis,['carcinoma arising in nasal papillomatosis'],8415,,,C1332840,,C27389,,,,,,
mondo:0004557,congenital fibrosarcoma,"['infantile fibrosarcoma (morphologic abnormality)', 'IFS', 'infantile fibrosarcoma (congenital fibrosarcoma)', 'congenital fibrosarcoma', 'infantile fibrosarcoma']",8418,,,C0334459,,C4244,,,171.9,,,
mondo:0004558,thyroid gland macrofollicular adenoma,"['macrofollicular adenoma', 'colloid adenoma', 'macrofollicular adenoma (morphologic abnormality)']",8419,,,C0334329,,C4161,,,,,,
mondo:0004559,malignant glandular tumor of peripheral nerve sheath,"['malignant glandular peripheral nerve sheath tumour', 'malignant glandular tumor of the peripheral nerve sheath', 'malignant glandular tumour of the peripheral nerve sheath', 'malignant glandular tumor of peripheral nerve sheath', 'glandular malignant peripheral nerve sheath tumor', 'malignant glandular peripheral nerve sheath tumor', 'glandular malignant peripheral nerve sheath tumour', 'malignant glandular peripheral nerve sheath neoplasm', 'glandular MPNST', 'malignant glandular schwannoma', 'malignant glandular neoplasm of the peripheral nerve sheath', 'malignant glandular neoplasm of peripheral nerve sheath']",8420,,,C1333821,,C6560,,,171.9,,,
mondo:0004560,follicular infundibulum tumor,"['tumor of follicular infundibulum', 'tumour of follicular infundibulum', 'tumour of the follicular infundibulum', 'tumor of the follicular infundibulum', 'basal cell hamartoma with follicular differentiation', 'neoplasm of the follicular infundibulum', 'follicular infundibulum neoplasm']",8426,,,C0346006,,C4469,,,239.2,,,
mondo:0004561,retinal melanoma,"['melanoma of the retina', 'melanoma of retina', 'retina melanoma (disease)', 'malignant melanoma of retina', 'retinal melanoma', 'malignant melanoma of the retina', 'malignant retinal melanoma']",8427,,,C0853394,,C8601,,,,,,
mondo:0004562,breast apocrine carcinoma in situ,"['apocrine carcinoma in situ of the breast', 'apocrine carcinoma in situ of breast', 'apocrine breast carcinoma in situ']",8428,,,C1332315,,C5140,,,,,,
mondo:0004563,physiological polycythemia,,8431,,,C0856817,,C27311,,,,,,
mondo:0004564,thyroid malformation,['thyroid gland malformation'],8433,,,,,C27331,,,,,,
mondo:0004565,intestinal obstruction,['bowel obstruction'],8437,,,C0021843,,C9175,,D007415,560.9,,,
mondo:0004566,postgastrectomy syndrome,['postgastric surgery syndrome'],8439,,,C0032763,,,,D011178,564.2,,,
mondo:0004567,ileus,['ileus of intestine'],8440,,,C1258215,,C37979,,D045823,,,,
mondo:0004568,paralytic ileus,"['paralytic ileus', 'paralytic ileus (disease)']",8442,,,C0030446,,C93045,,D007418,560.1,,,0002590
mondo:0004569,brachial plexus neuropathy from injury,"['brachial plexus lesions', 'brachial plexus lesion']",8443,,,C0006091,,,,,353.0,,,
mondo:0004570,intestinal volvulus,"['volvulus', 'intestinal volvulus', 'twist of intestine, bowel, or colon']",8445,,,C0042961,,,1000989,D045822,560.2,K56.2,,
mondo:0004571,intestinal impaction,,8448,,,,,,,,560.39,,,
mondo:0004572,cyclothymic disorder,"['cyclothymia', 'affective personality disorder', 'cyclothymic personality', 'cycloid personality']",845,,,,,,,D003527,301.13,F34.0,,
mondo:0004573,ariboflavinosis,"['riboflavin deficiency', 'vitamin B2 deficiency']",8454,615026,,,,,,,266.0,,,
mondo:0004574,pyridoxine deficiency anemia,"['vitamin B6 deficiency syndrome', 'deficiency, vitamin B 6', 'pyridoxine deficiency', 'vitamin deficiency, B6', 'B6 deficiency, vitamin', 'deficiencies, B6 vitamin', 'deficiency, B6 vitamin', 'deficiencies, vitamin B6', 'B6 deficiencies, vitamin', 'vitamin B6 deficiencies', 'deficiency, pyridoxine', 'deficiency, vitamin B6', 'vitamin B6 deficiency', 'vitamin deficiencies, B6', 'pyridoxine Deficincy', 'B6 vitamin deficiency', 'B6 vitamin deficiencies']",8455,,,,,C85221,,D026681,281.8,,,
mondo:0004575,choline deficiency disease,['choline deficiency'],8456,,,C0008412,,,,D002796,266.2,,,
mondo:0004577,corneal ulcer,"['Ulcer, corneal', 'ulcer disease of cornea', 'cornea ulcer disease']",8463,,,C0010043,,C50515,,D003320,370.00,H16.0,,0200020
mondo:0004578,flat retinoschisis,,8464,,,C0154817,,,,,361.11,,,
mondo:0004579,retinoschisis,,8465,,,C0152439,,C85046,,D041441,361.10,,,
mondo:0004580,retinal degeneration,"['degeneration of retina', 'retina degeneration', 'retina, Degeneration Of']",8466,,,,,C34979,,D012162,,,,
mondo:0004582,rheumatic myocarditis,"['acute rheumatic myocarditis (disorder) [ambiguous]', 'rheumatic degeneration of myocardium', 'acute rheumatic myocarditis', 'rheumatic fever with myocarditis', 'rheumatic myocarditis', 'rheumatoid myocarditis', 'acute rheumatic carditis', 'active rheumatic fever with myocarditis']",8481,,,C0155557,,C35202,,,398.0,,,
mondo:0004583,transient retinal arterial occlusion,"['transient retinal arterial occlusion', 'transient arterial retinal occlusion', 'retinal transient arterial occlusion']",8482,,,C0154840,,C35193,,,362.34,,,
mondo:0004584,maple bark strippers^ lung,"['maple-bark strippers^ lung', 'maple bark stripper^s disease', 'maple bark disease', 'alveolitis due to cryptostroma corticale', 'maple bark-strippers^ lung', 'maple bark stripper^s lung']",8484,,,C0155890,,,,,495.6,,,
mondo:0004585,polyhydramnios,"['polyhydramnios (disease)', 'polyhydramnios']",8488,,,,,,,D006831,657.00,,,0001561
mondo:0004586,rheumatoid lung disease,['rheumatoid lung'],849,,,C0994344,,,,,714.81,,,
mondo:0004587,hereditary night blindness,"['congenital night blindness', 'hereditary night blindness', 'Oguchi^s disease']",8498,,,,,,,C537743,368.61,,,
mondo:0004588,night blindness,['nyctalopia'],8499,,,C0028077,,C34850,,D009755,368.69,H53.6,,
mondo:0004591,impetigo herpetiformis,,8503,,,C1314968,,,1000715,,694.3,,,
mondo:0004592,impetigo,,8504,,,C0021099,,C99088,1000714,D007169,684,L01,,
mondo:0004593,Bartholin duct cyst,"['Bartholin^s duct cyst', 'cyst of Bartholin^s gland', 'Bartholin^s cyst', 'cyst of Bartholin^s gland duct']",851,,,C0004767,,,,,616.2,N75.0,,
mondo:0004594,puerperal pulmonary embolism,,8512,,,,,,,,673.81,,,
mondo:0004596,cor pulmonale,"['heart disease, pulmonary', 'disease, pulmonary heart', 'diseases, pulmonary heart', 'cardiopulmonary disease', 'cor pulmonale', 'pulmonary heart diseases', 'pulmonary heart disease', 'heart diseases, pulmonary']",8515,,,C0034072,,,,D011660,,I27.81,,
mondo:0004597,pulmonary embolism and infarction,"['infarction, pulmonary', 'lung infarction']",8516,,,,,C50714,1001408,D054060,415.19,,,
mondo:0004598,acute cor pulmonale,"['acute pulmonary heart disease', 'cor pulmonale, acute']",8517,,,C0155672,,,,,415.0,,,
mondo:0004599,barbiturate abuse,,8519,,,,,,,,305.43,,,
mondo:0004600,monocytic leukemia,"['schilling^s leukemia', 'schilling^s leukaemia']",8527,,,,,,,,206.91,,,
mondo:0004601,ulcer of lower limbs,"['Ulcer of calf', 'Ulcer of thigh', 'Ulcer of ankle', 'Ulcer of heel and midfoot']",8529,,,,,,0007068,,707.13,,,
mondo:0004603,collagenopathy,,,,,,,,,,,,,
mondo:0004604,"Hodgkin^s lymphoma, lymphocytic-histiocytic predominance","['lymphocyte rich classical Hodgkin^s lymphoma', 'lymphocyte rich classical Hodgkin^s disease', 'lymphocyte rich Hodgkin lymphoma', 'Hodgkin lymphoma, lymphocytic-histiocytic predominance', 'Hodgkin lymphoma, lymphocyte-rich', 'lymphocyte-rich Classic Hodgkin lymphoma', 'lymphocyte-rich classical Hodgkin^s lymphoma', 'Hodgkin^s disease, lymphocyte predominance [obs]', 'lymphocyte rich Hodgkin^s lymphoma', 'lymphocyte rich classical Hodgkin lymphoma', 'lymphocyte-rich classical Hodgkin lymphoma', 'lymphocyte rich Hodgkin^s disease', 'Hodgkin^s disease, lymphocyte predominance', 'LRCHL', 'classic Hodgkin lymphoma, lymphocyte-rich type']",8543,,98845,,,C6913,,,201.4,,10020231,
mondo:0004605,chronic ulcer of skin,"['indolent ulcer (morphologic abnormality)', 'callous ulcer', 'indolent ulcer', 'callous ulcer (morphologic abnormality)']",8549,,,C0157738,,,0007066,,707.9,,,
mondo:0004607,vallecula cancer,"['malignant neoplasm of epiglottic vallecula', 'malignant epiglottic vallecula neoplasm', 'cancer of epiglottic vallecula', 'epiglottic vallecula cancer', 'malignant tumor of vallecula', 'malignant tumour of vallecula']",8556,,,C0153386,,,,,146.3,C10.0,,
mondo:0004608,oropharynx cancer,"['malignant tumour of the oropharynx', 'oropharynx cancer', 'malignant oropharynx neoplasm', 'malignant tumor of oropharynx', 'malignant tumor of mesopharynx', 'malignant tumor of the oropharynx', 'oropharyngeal carcinoma', 'primary malignant neoplasm of lateral wall of oropharynx', 'cancer of oropharynx', 'oropharyngeal cancer', 'malignant oropharyngeal neoplasm', 'malignant tumour of oropharynx', 'malignant tumor of posterior wall of oropharynx', 'malignant neoplasm of the oropharynx', 'malignant neoplasm of junctional region of oropharynx', 'malignant oropharyngeal tumour', 'malignant tumour of posterior wall of oropharynx', 'malignant neoplasm of posterior wall of oropharynx', 'malignant neoplasm of oropharynx', 'malignant oropharyngeal tumor', 'malignant neoplasm of lateral wall of oropharynx', 'malignant tumour of mesopharynx']",8557,,,C3165521,,C7398,1001931,D009959,146.9,C10,,
mondo:0004609,herpes simplex infectious disease,"['Herpesvirus hominis disease', 'Simplexvirus caused disease or disorder']",8566,,,C0019348,,,1002022,D006561,058.89,B00,,
mondo:0004611,soft palate cancer,"['malignant soft palate tumor', 'malignant soft palate tumour', 'malignant tumor of the soft palate', 'malignant neoplasm of soft palate', 'malignant tumour of the soft palate', 'malignant soft palate neoplasm', 'malignant tumour of soft palate', 'malignant tumor of soft palate', 'soft palate cancer', 'malignant neoplasm of the soft palate', 'cancer of soft palate']",8578,,,C0153376,,C3529,,,145.3,C05.1,,
mondo:0004612,malignant histiocytosis,"['histiocytic disorder, malignant', 'malignant histiocytic disease', 'histiocytic medullary reticulosis', 'malignant reticulosis', 'Stewart^s granuloma', 'malignant histiocytic disorders', 'disorders, malignant histiocytic', 'malignant midline reticulosis']",8580,,,C0019623,,C7202,1001499,D054747,202.3,C96.A,,
mondo:0004613,acute intestinal ischemia,"['acute intestinal ischemia', 'acute intestinal vascular insufficiency']",8590,,,C0001363,,C34356,,,557.0,,,
mondo:0004614,chronic monocytic leukemia,"['monocytic leukemia, chronic']",8593,,,C0023466,,C34774,,,206.11,,,
mondo:0004615,upper gum cancer,"['malignant tumour of upper gingiva', 'cancer of gingiva of upper jaw', 'malignant tumour of upper gum', 'malignant tumor of upper gingiva', 'malignant neoplasm of gingiva of upper jaw', 'malignant tumor of upper gum', 'gingiva of upper jaw cancer', 'malignant gingiva of upper jaw neoplasm']",8601,,,C0153365,,,,,143.0,,,
mondo:0004616,herpetic whitlow,"['Simplexvirus caused paronychia (disease)', 'herpetic felon']",8607,,,C0153042,,C128402,,,054.6,,,
mondo:0004617,recurrent hypersomnia,['primary recurrent hypersomnia'],8619,,,C0751226,,,,,327.13,G47.13,,
mondo:0004618,diplegia of upper limb,"['diplegia of upper limbs', 'diplegia, upper']",862,,,C0154701,,,,,344.2,,,
mondo:0004619,measles,"['morbilli', 'rubeola infection', 'Measles morbillivirus caused disease or disorder', 'rubeola']",8622,,,C0025007,,C96406,1002025,D008457,055,B05,,
mondo:0004620,"Hodgkin^s lymphoma, lymphocytic depletion","['adult lymphocyte-depleted classical Hodgkin lymphoma', 'classic Hodgkin lymphoma, lymphocyte-depleted type', 'Hodgkin^s disease, lymphocytic depletion', 'lymphocyte-depleted classical Hodgkin lymphoma', 'Hodgkin lymphoma, lymphocyte depletion', 'Adult lymphocyte-depleted Classic Hodgkin lymphoma', 'Hodgkin^s lymphocytic depletion of unspecified site', 'adult lymphocyte depleted Hodgkin^s lymphoma', 'adult LDHD', 'Hodgkin^s disease, lymphocytic depletion, unspecified site, extranodal and solid organ sites', 'adult lymphocyte depletion Hodgkin^s disease', 'adult HDLD', 'adult lymphocyte depleted Hodgkin lymphoma', 'adult lymphocyte depleted classical Hodgkin lymphoma', 'Hodgkin^s disease, lymphocytic depletion NOS (morphologic abnormality)']",8628,,98846,,,C9125,,,201.7,,,
mondo:0004621,upper lip cancer,"['malignant neoplasm of upper lip', 'upper lip cancer', 'malignant upper lip neoplasm', 'cancer of upper lip']",8630,,,,,,,,140.3,,,
mondo:0004622,chronic intestinal vascular insufficiency,"['chronic mesenteric ischemia', 'CMI - chronic mesenteric ischaemia']",8633,,,C0311262,,,,,557.1,,,
mondo:0004624,uvula cancer,"['malignant uvula tumor', 'malignant uvula neoplasm', 'malignant uvular tumour', 'cancer of palatine uvula', 'malignant uvular tumor', 'malignant tumor of uvula', 'malignant palatine uvula neoplasm', 'malignant tumour of uvula', 'palatine uvula cancer', 'malignant neoplasm of palatine uvula', 'malignant uvula tumour', 'malignant uvular neoplasm']",8635,,,C0153377,,C35177,,,145.4,,,
mondo:0004625,phlebitis,['vein inflammation'],864,,,,,C38003,1001395,D010689,,,,
mondo:0004627,duodenitis,"['hemorrhagic duodenitis', 'duodenum inflammation']",8643,,,C0013298,,C94409,,D004382,535.60,K29.8,,
mondo:0004628,gastroduodenitis,['peptic ulcer gastroduodenitis'],8644,,,C0267166,,,,,535.50,,,
mondo:0004629,subacute delirium,,8645,,,,,,,,293.1,,,
mondo:0004630,substance-induced psychosis,,8646,,,,,,,,293.89,,,
mondo:0004631,tongue cancer,"['tongue neoplasm malignant stage unspecified', 'tongue neoplasm, malignant', 'malignant neoplasm of tip and lateral border of tongue', 'malignant neoplasm of fixed part of tongue NOS', 'malignant tumour of tongue', 'malignant neoplasm of mobile part of tongue NOS', 'malignant neoplasm of fixed part of tongue', 'malignant neoplasm of tip and/or lateral border of tongue', 'malignant neoplasm of anterior two-thirds of tongue', 'malignant tumour of base of tongue', 'malignant neoplasm of base of tongue', 'malignant tumor of posterior tongue', 'malignant tumor of anterior two-thirds of tongue', 'malignant tumor of the tongue', 'malignant neoplasm of tongue, NOS', 'malignant tumour of posterior tongue', 'tongue neoplasm malignant', 'malignant neoplasm of the tongue', 'malignant tumor of mobile part of tongue', 'malignant neoplasm of dorsum of tongue', 'malignant neoplasm of anterior 2/3 of tongue', 'malignant neoplasm of anterior two-thirds of tongue, part unspecified', 'cancer of tongue', 'malignant neoplasm of border of tongue', 'malignant neoplasm of ventral tongue surface', 'malignant tumour of the tongue', 'malignant neoplasm of tongue, tip and lateral border', 'malignant tumour of anterior two-thirds of tongue', 'malignant tumour of lingual tonsil', 'malignant neoplasm of dorsal tongue NOS', 'malignant neoplasm of dorsal surface of tongue', 'malignant neoplasm of dorsal tongue', 'malignant tumour of mobile part of tongue', 'malignant neoplasm of tongue NOS', 'malignant neoplasm of tongue', 'malignant tumor of lingual tonsil (disorder)', 'malignant tongue tumour', 'malignant tumor of base of tongue', 'malignant tumor of lingual tonsil', 'malignant neoplasm of mobile part of tongue', 'malignant neoplasm of lingual tonsil', 'malignant tongue tumor', 'malignant tumour of lingual tonsil (disorder)', 'malignant tongue neoplasm', 'tongue carcinoma', 'malignant neoplasm of ventral surface of tongue', 'malignant tumor of tongue', 'malignant neoplasm of junctional zone of tongue', 'tongue cancer', 'malignant neoplasm of other sites of tongue']",8649,,,,,C9345,,D014062,141.9,,,
mondo:0004633,"Hodgkin^s lymphoma, mixed cellularity","['mixed cellularity Hodgkin^s disease', 'MCCHL', 'classic Hodgkin lymphoma, mixed cellularity type', 'Mixed cellularity Classic Hodgkin lymphoma', 'mixed cellularity classical Hodgkin lymphoma', 'Hodgkin^s disease mixed cellularity', 'MCHL', 'mixed cellularity Hodgkin lymphoma', 'Hodgkin^s disease, mixed cellularity of unspecified site', 'Hodgkin^s disease, mixed cellularity', 'Hodgkin lymphoma, mixed cellularity', 'Hodgkin^s lymphoma mixed cellularity', 'mixed cellularity Hodgkin^s lymphoma']",8654,,98844,,,C3517,,,201.6,,,
mondo:0004634,vein disorder,"['vein disease or disorder', 'disorder of vein', 'vein disease', 'disease of vein']",866,,,C0235522,,C35279,,,453,,,
mondo:0004635,postcricoid region cancer,"['malignant tumour of the postcricoid area', 'malignant tumor of the postcricoid area', 'malignant tumor of pharyngoesophageal junction', 'malignant neoplasm of postcricoid area', 'malignant postcricoid neoplasm', 'malignant neoplasm of the postcricoid area', 'malignant tumour of pharyngoesophageal junction', 'malignant tumour of postcricoid area', 'malignant tumor of postcricoid area', 'malignant postcricoid tumour', 'malignant postcricoid tumor']",8660,,,C0496769,,C9323,,,148.0,,,
mondo:0004636,lip carcinoma in situ,"['lip in situ carcinoma', 'stage 0 Lip cancer aJCC v6 and v7', 'stage 0 carcinoma of Lip', 'stage 0 carcinoma of the Lip', 'carcinoma in situ of the Lip', 'stage 0 cancer of the Lip', 'stage 0 Lip cancer aJCC v6', 'stage 0 cancer of Lip', 'stage 0 lip carcinoma', 'stage 0 Lip cancer aJCC v7', 'stage 0 Lip cancer', 'carcinoma in situ of lip']",8661,,,C4316815,,C4588,,,230.0,,,
mondo:0004637,aryepiglottic fold cancer,"['malignant neoplasm of hypopharyngeal aspect of aryepiglottic fold', 'aryepiglottic fold cancer', 'malignant tumour aryepiglottic fold - hypopharyngeal aspect', 'malignant neoplasm of aryepiglottic fold', 'malignant aryepiglottic fold neoplasm', 'cancer of aryepiglottic fold', 'malignant tumor aryepiglottic fold - hypopharyngeal aspect']",8663,,,,,,,,148.2,C13.1,,
mondo:0004638,lymphosarcoma,"['malignant lymphoma (category)', 'diffuse lymphoma', 'lymphosarcoma']",8675,,,,,C27824,,,200.7,,,
mondo:0004639,perinatal necrotizing enterocolitis,"['pseudomembranous enterocolitis in newborn', 'perinatal necrotising enterocolitis', 'enterocolitis, necrotizing', 'necrotizing enterocolitis in foetus or newborn', 'necrotizing enterocolitis in fetus or newborn', 'necrotizing enterocolitis', 'enterocolitis necrotizing']",8677,,,,,,,,,,,
mondo:0004640,alcoholic gastritis,"['alcoholic gastritis', 'alcoholic gastritis, without mention of haemorrhage', 'alcoholic gastritis, with hemorrhage', 'alcoholic gastritis, without mention of hemorrhage', 'alcoholic gastritis, with haemorrhage']",8680,,,C0156076,,C26977,,,535.30,K29.2,,
mondo:0004641,skin carcinoma in situ,"['stage 0 skin cancer aJCC v6', 'stage 0 skin carcinoma', 'nonmelanoma carcinoma in situ', 'carcinoma in situ of the skin', 'stage 0 skin cancer aJCC v7', 'stage 0 skin cancer', 'zone of skin in situ carcinoma', 'skin carcinoma in situ', 'stage 0 zone of skin carcinoma', 'stage 0 nonmelanoma skin carcinoma in situ', 'skin carcinoma stage 0', 'carcinoma in situ of skin', 'cutaneous carcinoma in situ', 'carcinoma of the skin stage 0', 'carcinoma of skin stage 0', 'carcinoma in situ of zone of skin', 'skin cancer stage 0']",8687,,,C0154073,,C3640,,,232.9,D04,,
mondo:0004642,tonsillar pillar cancer,"['malignant tumor of tonsillar pillar', 'malignant neoplasm of tonsillar pillars, posterior', 'malignant tumour of tonsillar pillar', 'malignant neoplasm of tonsillar pillar']",8688,,,C0153385,,,,,146.2,C09.1,,
mondo:0004643,myeloid leukemia,"['leukaemia myeloid', 'myelocytic leukemia', 'myelogenous leukaemia', 'non-lymphoblastic leukaemia', 'leukaemia granulocytic', 'leukemia myelogenous', 'myelogenous leukemia', 'non-lymphocytic leukaemia', 'myeloid leukemia', 'myeloid granulocytic leukemia', 'leukaemia myelogenous', 'myelocytic leukaemia', 'leukemia granulocytic', 'leukemia myeloid', 'non-lymphocytic leukemia', 'leukemia, granulocytic, malignant', 'non-lymphoblastic leukemia', 'myeloid granulocytic leukaemia']",8692,,,C0023470,,C3172,,D007951,205.90,,,
mondo:0004644,subacute monocytic leukemia,,8696,,,C0152275,,,,,206.20,,,
mondo:0004645,cheek mucosa cancer,"['malignant tumour of buccal mucosa', 'malignant buccal mucosa tumor', 'malignant neoplasm of the buccal mucosa', 'cancer of buccal mucosa', 'malignant tumor of the buccal mucosa', 'malignant neoplasm of buccal mucosa', 'malignant neoplasm of cheek, inner aspect', 'malignant tumor of buccal mucosa', 'malignant tumour of the buccal mucosa', 'buccal mucosa cancer', 'malignant buccal mucosa neoplasm', 'malignant buccal mucosa tumour']",8702,,,C0153373,,C9320,,,145.0,,,
mondo:0004646,decubitus ulcer,"['decubitus ulcer', 'pressure sores', 'decubitus ulcer, lower back', 'decubitus ulcer, elbow', 'decubitus (pressure) ulcer', 'decubitus ulcer, other site', 'pressure ulcer', 'decubitus ulcer, upper back', 'decubitus ulcer any site', 'bedsore']",8717,,,C0011127,,,0007067,D003668,707.00,,,
mondo:0004647,in situ carcinoma,"['intraepithelial carcinoma', 'CIS', 'epithelial tumor, in situ, malignant', 'carcinoma, in situ, malignant', 'carcinoma in situ', 'stage 0 disease', 'non-invasive carcinoma']",8719,,,C0007099,,C2917,,D002278,234.9,,,
mondo:0004648,vascular dementia,"['multi infarct dementia', 'multifocal dementia', 'vascular dementia']",8725,,,C0011269,,C34525,0004718,D015140,290.4,,,
mondo:0004649,anaerobic pneumonia,['pneumonia due to anaerobes'],873,,,C1443976,,,,,482.89,,,
mondo:0004650,malignant carotid body paraganglioma,"['malignant carotid body tumor (morphologic abnormality)', 'malignant tumour of carotid body', 'malignant neoplasm of carotid body', 'malignant carotid body tumour', 'malignant carotid body neoplasm', 'chemodectoma, malignant', 'malignant carotid body paraganglioma', 'malignant carotid body tumour (morphologic abnormality)', 'malignant tumor of the carotid body', 'cancer of carotid body', 'malignant neoplasm of the carotid body', 'malignant tumour of the carotid body', 'carotid body cancer', 'malignant tumor of carotid body', 'malignant carotid body tumor', 'carotid body paraganglioma, malignant']",8731,,,C0153656,,C3574,,,194.5,C75.4,,
mondo:0004651,smallpox,"['Variola', 'Variola virus caused disease or disorder', 'variola virus VAR infection', 'ordinary smallpox', 'smallpox virus infection', 'variola virus infection']",8736,,,C0037354,,C35027,,D012899,050.9,B03,,
mondo:0004652,bacterial pneumonia,"['gram-negative pneumonia', 'Bacteria caused pneumonia', 'pneumonia due to other gram-negative bacteria']",874,,,C0004626,,C26704,1001272,D018410,482.9,,,
mondo:0004653,"atypical chronic myeloid leukemia, BCR-ABL1 negative","['subacute granulocytic leukemia', 'atypical chronic myeloid leukemia BCR-ABL1 negative', 'subacute myeloid leukaemia', 'atypical chronic myeloid leukaemia', 'atypical chronic myeloid leukaemia BCR-ABL1 negative', 'subacute myeloid leukemia', 'aCML', 'subacute granulocytic leukaemia', 'subacute myelogenous leukaemia', 'subacute myelogenous leukemia', 'atypical CML', 'atypical chronic myeloid leukemia', 'atypical chronic myeloid leukemia, BCR-ABL1 Negative']",8747,,98824,,,C3519,,,,,10054651,
mondo:0004656,rubella,"['Rubella infection', 'Rubella virus caused disease or disorder', 'three-Day Measles', 'three day measles', 'german measles']",8781,,,C0035920,,C85051,1002026,D012409,056,B06,,
mondo:0004657,disseminated chorioretinitis,,8787,,,C0154879,,,,,363.10,,,
mondo:0004658,breast carcinoma in situ,"['stage 0 breast cancer aJCC v7', 'non-invasive carcinoma of the breast', 'breast cancer in situ', 'carcinoma in situ of the breast', 'stage 0 breast carcinoma in situ', 'in situ breast cancer', 'non-infiltrating carcinoma of breast', 'stage 0 breast carcinoma', 'stage 0 breast cancer', 'non-invasive breast carcinoma', 'carcinoma in situ of breast', 'stage 0 breast cancer aJCC v6', 'stage 0 carcinoma of breast', 'breast cancer stage 0', 'stage 0 carcinoma of the breast', 'breast carcinoma in situ', 'non-infiltrating carcinoma of the breast', 'stage 0 breast cancer aJCC v6 and v7', 'non-infiltrating breast carcinoma', 'breast in situ carcinoma', 'non-invasive carcinoma of breast']",8791,,,C0154084,,C3641,,D000071960,233.0,,,
mondo:0004659,eye carcinoma in situ,"['stage 0 eye carcinoma', 'eye in situ carcinoma', 'carcinoma in situ of eye', 'stage 0 eyeball of camera-type eye carcinoma', 'carcinoma in situ of eyeball of camera-type eye']",8792,,,C0154094,,,,,234.0,,,
mondo:0004660,lung carcinoma in situ,"['stage 0 lung cancer aJCC v6', 'carcinoma in situ of lung', 'stage 0 lung cancer aJCC v7', 'bronchial carcinoma in situ', 'stage 0 lung cancer aJCC v6 and v7', 'lung in situ carcinoma', 'stage 0 lung cancer', 'stage 0 lung carcinoma']",8800,,,C0685053,,C27467,,,231.2,,,
mondo:0004661,trachea carcinoma in situ,"['stage 0 trachea carcinoma', 'severe epithelial dysplasia of trachea', 'carcinoma in situ of the trachea', 'tracheal carcinoma in situ', 'trachea in situ carcinoma', 'trachea carcinoma in situ', 'carcinoma in situ of trachea']",8802,,,C0154070,,C3639,,,231.1,D02.1,,
mondo:0004662,heterophyiasis,"['Heterophyes infection', 'infections, Heterophyes', 'Heterophyes infectious disease']",882,,,C0152071,,C128389,,,121.6,,,
mondo:0004663,colon carcinoma in situ,"['carcinoma in situ of colon', 'stage 0 colon cancer aJCC v6', 'stage 0 colon cancer aJCC v6 and v7', 'stage 0 carcinoma of the colon', 'stage 0 colon cancer aJCC v7', 'stage 0 colonic carcinoma', 'stage 0 carcinoma of colon', 'colon cancer stage 0', 'colon carcinoma in situ', 'colonic carcinoma in situ', 'stage 0 colon cancer', 'stage 0 colon carcinoma', 'colon in situ carcinoma', 'carcinoma in situ of the colon']",8826,,,C0154061,,C3638,,,230.3,D01.0,,
mondo:0004664,helminthiasis,"['parasitic helminthiasis infectious disease', 'helminthosis', 'helminth infection', 'worm infection', 'helminthiasis']",883,,,C0018889,,C84751,1001342,D006373,128.9,B65-B83,,
mondo:0004665,nodular sclerosis classical Hodgkin lymphoma,"['nodular sclerosis Hodgkin lymphoma', 'nodular sclerosis Hodgkin^s lymphoma', 'NSCHL', 'Hodgkin^s disease, nodular sclerosis NOS (morphologic abnormality)', 'Hodgkin^s lymphoma, nodular sclerosis', 'NSHL', 'Hodgkin^s nodular sclerosis', 'nodular sclerosis Hodgkin^s disease', 'NSHD', 'nodular sclerosis Classic Hodgkin lymphoma', 'nodular sclerosis classical Hodgkin lymphoma', 'Hodgkin^s disease, nodular sclerosis', 'Hodgkin^s disease nodular sclerosis', 'Hodgkin^s disease, nodular sclerosis of unspecified site', 'Hodgkin lymphoma, nodular sclerosis', 'classical Hodgkin lymphoma, nodular sclerosis']",8838,,,,,C3518,0004708,,201.5,,,
mondo:0004666,metagonimiasis,"['infection by Metagonimus yokogawai', 'infections, Metagonimus yokogawai', 'Metagonimus yokogawai infection']",884,,,C0025530,,C128390,,,121.5,,,
mondo:0004667,sublingual gland cancer,"['malignant tumour of the sublingual gland', 'malignant sublingual gland tumour', 'malignant tumour of sublingual gland', 'malignant sublingual gland tumor', 'malignant neoplasm of the sublingual gland', 'malignant tumor of sublingual gland', 'sublingual gland cancer', 'cancer of sublingual gland', 'malignant tumor of the sublingual gland', 'malignant sublingual gland neoplasm', 'malignant neoplasm of sublingual gland']",8849,,,C0153361,,C3527,,,142.2,,,
mondo:0004668,fascioliasis,"['liver flukes', 'infection by fasciola', 'Fasciolosis', 'sheep liver fluke infection', 'fasciola hepatica infection']",885,,,C1331532,,C128387,1001324,D005211,121.3,B66.3,,
mondo:0004669,salivary gland cancer,"['malignant neoplasm of saliva-secreting gland', 'malignant salivary gland neoplasm', 'malignant neoplasm of major salivary gland', 'malignant saliva-secreting gland neoplasm', 'malignant tumour of salivary gland', 'salivary gland cancer', 'malignant neoplasm of salivary gland duct', 'malignant tumor of salivary gland', 'malignant neoplasm of salivary gland', 'malignant tumor of the salivary gland', 'cancer of salivary gland', 'cancer of saliva-secreting gland', 'malignant tumour of the salivary gland', 'malignant salivary gland tumor', 'malignant salivary gland tumour', 'cancer of the salivary gland', 'malignant tumour of the major salivary gland', 'malignant neoplasm of the salivary gland']",8850,,,,,C3811,,D012468,142.8,C08,,
mondo:0004670,lupus erythematosus,"['lupus erythematosus', 'lupus']",8857,,,C0409974,,C27153,,,695.4,L93,,
mondo:0004671,penis carcinoma in situ,"['penile intraepithelial neoplasia grade III', 'Bowen^s disease of penis', 'penile carcinoma in situ aJCC v7', 'Queyrat^s erythroplasia', 'stage 0 penis carcinoma', 'grade III squamous intraepithelial lesion of penis', 'penile carcinoma in situ', 'Bowen disease of the penis', 'carcinoma in situ of penis', 'erythroplasia of Queyrat', 'carcinoma in situ of the penis', 'penis in situ carcinoma', 'grade III penile intraepithelial neoplasia', 'grade III squamous intraepithelial lesion of the penis', 'Queyrat erythroplasia', 'Bowen^s disease of the penis', 'stage 0 penile carcinoma in situ']",8872,,,C0154089,,C27790,,,233.5,,,
mondo:0004672,fasciolopsiasis,"['infection by Fasciolopsis buski', 'infectious disease by Fasciolopsis']",888,,,C0015656,,C128388,,,121.4,B66.5,,
mondo:0004673,lower lip cancer,"['malignant neoplasm of lower lip', 'cancer of lower lip', 'malignant lower lip neoplasm', 'lower lip cancer']",8883,,,C0432520,,,,,140.1,,,
mondo:0004674,chorioretinitis,"['chorioretinitis (disease)', 'chorioretinitis', 'retinochoroiditis']",8886,,,C0008513,,C110923,,D002825,363.20,,,0012424
mondo:0004675,mitochondrial encephalomyopathy,,890,,,C0162666,,,,D017237,277.87,,,
mondo:0004677,tinea nigra,"['keratomycosis nigricans', 'microsporosis nigra', 'Tinea palmaris nigra', 'infection by Cladosporium werneckii']",8912,,,C0152067,,,,,111.1,B36.1,,
mondo:0004678,dermatophytosis,"['fungal skin disease', 'dermatomycosis', 'skin disease, fungal', 'fungal skin diseases', 'ringworm', 'skin diseases, fungal']",8913,,,C0011636,,C26745,,,110.9,B35,,
mondo:0004679,leukoplakia of vagina,"['vaginal leukoplakia', 'leukoplakia of the vagina']",8920,,,C0156385,,C3663,,,623.1,N89.4,,
mondo:0004680,primary thrombocytopenia,,8925,,,C0701157,,,,,287.39,,,
mondo:0004681,learning disability,"['Academic skill disorder', 'learning disorder']",8927,,,CN229495,,C89334,,D007859,315.2,,,
mondo:0004682,retromolar area cancer,"['neoplasm of retromolar area, malignant', 'malignant tumour of retromolar area', 'malignant tumor of retromolar area']",8930,,,,,,,,145.6,C06.2,,
mondo:0004684,plantar fibromatosis,"['Lederhose disease', 'superficial fibromatosis of plantar part of pes', 'plantar fibromatosis', 'Dupuytren^s contracture of foot', 'Ledderhose^s disease', 'plantar part of pes superficial Fibromatosis', 'plantar fascial fibromatosis', 'plantar part of pes superficial fibromatosis']",8936,,199251,,,C4680,1000481,C537000,728.71,,10035154,
mondo:0004685,Waldeyer^s ring cancer,"['tonsillar ring cancer', 'malignant tonsillar ring neoplasm', 'cancer of tonsillar ring', 'malignant tumor of Waldeyer^s ring', 'malignant neoplasm of tonsillar ring', 'Waldeyer ring cancer', 'malignant neoplasm of Waldeyer^s ring', 'malignant tumour of Waldeyer^s ring']",8937,,,C0153406,,,,,149.1,C14.2,,
mondo:0004686,lattice corneal dystrophy,"['familial amyloid neuropathy, Finnish type', 'lattice corneal dystrophy (disease)', 'lattice corneal dystrophy']",8943,,,C0155127,,,,,357.4,,,0001149
mondo:0004687,severe nonproliferative diabetic retinopathy,"['high risk non proliferative diabetic retinopathy', 'severe NPDR']",8946,,,C0730278,,,,,362.06,,,
mondo:0004689,inborn metal metabolism disorder,"['metal metabolism, inborn error', 'metal metabolism disorder']",896,,,C0025534,,,,D008664,,,,
mondo:0004690,tonsillar fossa cancer,"['malignant tumor of tonsillar fossa', 'malignant neoplasm of tonsillar fossa', 'malignant tumour of tonsillar fossa', 'tonsillar fossa cancer', 'cancer of tonsillar fossa', 'malignant tonsillar fossa neoplasm']",8969,,,C0153384,,,,,146.1,C09.0,,
mondo:0004691,autosomal dominant polycystic kidney disease,"['congenital biliary ectasias', 'ADPKD', 'polycystic kidney disease, autosomal dominant']",898,,730,CN119611,"['0.506', '0.2852', '-0.378', '0.0708', '0.2578', '-0.4255', '-0.615', '1.174', '-0.5522', '0.02917', '-0.1267', '-0.2322', '0.4387', '0.205', '-0.4875', '-0.9277', '-0.3816', '0.05356', '0.2311', '-0.2194', '-0.2822', '-0.03087', '-0.524', '0.077', '-0.01959', '-0.4336', '-0.307', '0.769', '0.806', '-0.2512', '0.916', '-0.09485', '0.561', '-0.01933', '0.3054', '-0.8633', '-0.527', '0.127', '0.54', '-0.2986', '0.52', '0.346', '0.5063', '0.07837', '0.10126', '-0.06445', '-0.5366', '-0.2537', '0.2035', '0.1138', '-0.09436', '0.1436', '0.6924', '-0.7275', '0.2507', '-0.3325', '0.09955', '0.3965', '-0.627', '-0.02545', '0.1711', '0.1272', '0.265', '-0.5156', '0.087', '-0.001655', '0.03372', '0.3125', '0.02524', '0.2214', '0.4126', '0.4873', '0.2041', '-0.4502', '0.1088', '0.099', '0.06573', '0.5063', '-0.0822', '0.11304', '-0.256', '0.1895', '0.483', '-0.1595', '0.05127', '0.061', '0.772', '-0.779', '-0.10114', '-0.246', '-0.1744', '0.3228', '-0.6147', '0.2922', '0.799', '0.2286', '0.2307', '-0.3728', '-0.2637', '-0.5225']",C84578,1001496,D016891,753.13,,,
mondo:0004693,squamous carcinoma in situ,"['stage 0 squamous cell carcinoma', 'squamous cell carcinoma in situ', 'cervical intraepithelial neoplasia grade III with severe dysplasia', 'carcinoma in situ of cervix', 'stage 0 uterine cervix carcinoma', 'squamous intraepithelial neoplasia, grade III', 'grade 3 squamous intraepithelial neoplasia', 'grade III SIN', 'epidermoid cell carcinoma in situ', 'squamous cell carcinoma in-situ', 'cervix Ca in situ', 'grade III squamous intraepithelial neoplasia', 'carcinoma, squamous cell, in situ, malignant', 'CIN III - carcinoma in situ of cervix', 'squamous carcinoma in situ', 'CIN III - severe dyskaryosis', 'epidermoid carcinoma in situ', 'carcinoma in situ of uterine cervix', 'uterine cervix in situ carcinoma', 'intraepithelial squamous cell carcinoma', 'severe dysplasia of cervix', 'CIN III', 'severe dysplasia of the cervix uteri', 'grade 3 SIN']",,,,C0334245,,C27093,,,,,,
mondo:0004694,hepatopulmonary syndrome,,900,,,C0600452,,,1001346,D020065,573.5,K76.81,,
mondo:0004695,liver lymphoma,"['primary hepatic lymphoma', 'primary liver lymphoma', 'lymphoma of the liver', 'liver lymphoma', 'lymphoma of liver', 'hepatic lymphoma']",901,,,C1112746,,C4949,,,,,,
mondo:0004696,larynx carcinoma in situ,"['stage 0 laryngeal carcinoma in situ', 'stage 0 laryngeal cancer aJCC v8', 'laryngeal carcinoma in situ', 'stage 0 carcinoma of the larynx', 'larynx carcinoma in situ', 'laryngeal cancer stage 0', 'stage 0 carcinoma of larynx', 'laryngeal carcinoma stage 0', 'stage 0 laryngeal throat cancer', 'stage 0 laryngeal cancer aJCC v6, v7, and V8', 'larynx in situ carcinoma', 'stage 0 laryngeal cancer aJCC v6', 'stage 0 laryngeal cancer aJCC v7', 'stage 0 laryngeal carcinoma', 'carcinoma in situ of the larynx', 'carcinoma in situ of larynx', 'stage 0 laryngeal cancer', 'stage 0 larynx carcinoma']",9011,,,C0154069,,C9100,,,231.0,D02.0,,
mondo:0004697,esophageal leukoplakia,"['esophageal leukoplakia (disease)', 'esophagus leukoplakia', 'leukoplakia of the esophagus', 'leukoplakia of the oesophagus', 'leukoplakia of esophagus', 'leukoplakia of oesophagus', 'esophageal leukoplakia', 'esophageal epidermoid metaplasia', 'oesophagus leukoplakia']",9021,,,C0267095,,C3953,,,530.83,,,0012859
mondo:0004698,intestine carcinoma in situ,"['carcinoma in situ of intestine', 'stage 0 intestine carcinoma', 'intestine in situ carcinoma']",9024,,,C0685941,,,,,230.7,,,
mondo:0004699,gastrointestinal lymphoma,"['gastrointestinal lymphoma', 'primary digestive system lymphoma', 'digestive system lymphoma', 'primary gastrointestinal lymphoma', 'lymphoma of digestive system']",903,,,C0740372,,C38162,,,202.80,,,
mondo:0004700,parotid gland cancer,"['malignant parotid tumor', 'malignant neoplasm of parotid gland', 'malignant parotid tumour', 'malignant parotid gland tumor', 'malignant tumor of parotid', 'cancer of the parotid', 'malignant tumor of parotid gland', 'malignant tumour of the parotid gland', 'malignant parotid neoplasm', 'malignant tumour of the parotid', 'malignant parotid gland tumour', 'cancer of parotid', 'malignant neoplasm of parotid', 'malignant neoplasm of the parotid', 'parotid gland cancer', 'cancer of parotid gland', 'malignant neoplasm of the parotid gland', 'malignant tumor of the parotid', 'malignant tumor of the parotid gland', 'malignant tumour of parotid', 'malignant tumour of parotid gland', 'cancer of the parotid gland', 'parotid cancer', 'malignant parotid gland neoplasm']",9036,,,C0747273,,C3525,,D010307,142.0,,,
mondo:0004701,uterine polyp,"['uterus polyp', 'polyp of uterus', 'polyp, uterus', 'polyp of endometrium', 'polyp of the uterus', 'uterine polyp', 'polyp of corpus uteri', 'endometrial/uterine polyp']",9042,,,C0156369,,C3662,,,621.0,N84.0,,
mondo:0004702,uterine cervix leukoplakia,"['leukoplakia of cervix', 'leukoplakia of uterine cervix', 'leukoplakia of the cervix uteri', 'cervix uteri leukoplakia', 'cervix leukoplakia', 'leukoplakia of the uterine cervix', 'leukoplakia of the cervix', 'leukoplakia of cervix (uteri)', 'cervical leukoplakia', 'leukoplakia of cervix uteri']",9043,,,C0269194,,C3976,,,622.2,N88.0,,
mondo:0004703,bladder carcinoma in situ,"['stage 0 urinary bladder carcinoma', 'bladder flat CIS', 'urinary bladder in situ carcinoma', 'bladder Ca in situ', 'stage 0is bladder urothelial carcinoma aJCC v6 and v7', 'urinary bladder flat CIS', 'stage 0is bladder urothelial carcinoma aJCC v6', 'flat carcinoma in situ of the urinary bladder', 'stage 0is carcinoma of urinary bladder', 'stage 0is bladder urothelial carcinoma aJCC v7', 'stage 0is carcinoma of the bladder', 'bladder flat carcinoma in situ', 'stage 0is bladder urothelial carcinoma', 'stage 0is urinary bladder carcinoma', 'stage 0is bladder urothelial cancer', 'carcinoma in situ of bladder', 'carcinoma in situ of urinary bladder', 'high grade bladder Intraurothelial neoplasia', 'stage 0is bladder cancer', 'cancer in situ of urinary bladder', 'flat carcinoma in situ of the bladder', 'stage 0is carcinoma of the urinary bladder', 'urinary bladder flat carcinoma in situ', 'flat CIS of the bladder', 'stage 0is bladder carcinoma', 'stage 0is carcinoma of bladder', 'flat CIS of the urinary bladder', 'carcinoma in situ of the urinary bladder']",9053,,,C0154091,,C3644,,,233.7,D09.0,,
mondo:0004705,liver solitary fibrous tumor,"['fibroma of the liver', 'liver solitary fibrous tumor', 'hepatic fibroma', 'liver localised fibrous tumour', 'liver localized fibrous tumor', 'liver fibroma', 'liver localized fibrous mesothelioma', 'fibroma of liver', 'liver localised fibrous mesothelioma']",907,,,C1333965,,C5752,,,,,,
mondo:0004706,discoid lupus erythematosus of eyelid,,9076,,,C0155180,,,,,373.34,,,
mondo:0004707,anal canal carcinoma in situ,"['anal canal in situ carcinoma', 'carcinoma in situ of anus', 'carcinoma in situ of anal canal', 'anal carcinoma in situ', 'stage 0 anal canal cancer aJCC v6', 'stage 0 anal canal cancer aJCC v6 and v7', 'stage 0 anal canal carcinoma aJCC v6 and v7', 'stage 0 anal canal cancer aJCC v7', 'anal carcinoma stage 0', 'stage 0 anal carcinoma aJCC v6 and v7', 'anal intraepithelial neoplasia grade III', 'stage 0 anal canal carcinoma', 'stage 0 anal carcinoma in situ', 'stage 0 anal canal cancer']",9087,,,C2242854,,C7794,,,230.6,,,
mondo:0004708,esophagus carcinoma in situ,"['esophagus in situ carcinoma', 'stage 0 carcinoma of the esophagus', 'stage 0 esophageal cancer aJCC v7', 'severe esophageal dysplasia', 'esophageal carcinoma in situ', 'carcinoma in situ of esophagus', 'stage 0 oesophagus carcinoma', 'oesophagus in situ carcinoma', 'carcinoma in situ of oesophagus', 'stage 0 carcinoma of the oesophagus', 'stage 0 esophagus carcinoma', 'stage 0 esophageal cancer', 'severe esophageal dysplasia aJCC v7', 'esophageal carcinoma in situ aJCC v7', 'stage 0 esophageal carcinoma in situ']",9095,,,C0154059,,C89771,,,230.1,D00.1,,
mondo:0004709,occipital lobe neoplasm,"['malignant neoplasm of occipital lobe', 'neoplasm of the occipital lobe', 'occipital lobe tumour', 'tumor of occipital lobe', 'occipital lobe tumor', 'tumour of occipital lobe', 'neoplasm of occipital lobe', 'tumour of the occipital lobe', 'occipital lobe neoplasm (disease)', 'tumor of the occipital lobe', 'occipital lobe neoplasm']",910,,,C1263889,,C5574,,,191.4,C71.4,,
mondo:0004710,uterus carcinoma in situ,"['uterus in situ carcinoma', 'stage 0 uterus carcinoma', 'carcinoma in situ of uterus']",9108,,,C0686237,,,,,233.2,,,
mondo:0004712,herpes simplex dermatitis,"['Herpes simplex eyelid dermatitis', 'Simplexvirus caused dermatitis', 'Herpes simplex virus dermatitis', 'eczema herpeticum', 'herpes simplex virus eyelid dermatitis', 'herpes simplex dermatitis', 'Herpes simplex dermatitis of eyelid', 'Herpes simplex dermatitis', 'eczema herpeticum (disorder) [ambiguous]']",9123,,,C0854331,,C35620,,D007617,054.41,B00.0,,
mondo:0004713,lower gum cancer,"['gingiva of lower jaw cancer', 'cancer of gingiva of lower jaw', 'malignant gingiva of lower jaw neoplasm', 'malignant tumour of lower gum', 'malignant neoplasm of gingiva of lower jaw', 'malignant tumour of lower gingiva', 'malignant tumor of lower gingiva', 'malignant tumor of lower gum']",9125,,,C0432581,,,,,143.1,,,
mondo:0004714,atrophic muscular disease,['atrophic muscular disorder'],913,,,,,C84574,,,,,,
mondo:0004715,liver carcinoma in situ,"['carcinoma in situ of liver', 'liver in situ carcinoma', 'carcinoma in situ of liver and biliary system', 'carcinoma in situ of liver, gallbladder and bile ducts', 'stage 0 liver carcinoma']",9132,,,C0345908,,,,,230.8,D01.5,,
mondo:0004716,stomach carcinoma in situ,"['carcinoma in situ of the stomach', 'carcinoma of stomach stage 0', 'stage 0 gastric carcinoma in situ', 'gastric carcinoma, stage 0', 'gastric carcinoma stage 0', 'stage 0 carcinoma of stomach', 'carcinoma of the stomach stage 0', 'stomach carcinoma in situ', 'stage 0 stomach cancer', 'stage 0 gastric cancer', 'stage 0 gastric cancer aJCC v7', 'stage 0 stomach carcinoma', 'gastric carcinoma in situ', 'stage 0 carcinoma of the stomach', 'stage 0 gastric cancer aJCC v6 and v7', 'carcinoma in situ of stomach', 'stomach carcinoma stage 0', 'stomach in situ carcinoma', 'stage 0 gastric (stomach) cancer', 'stage 0 gastric carcinoma', 'stage 0 gastric cancer aJCC v6']",9138,,,C0154060,,C7788,,,230.2,D00.2,,
mondo:0004717,peliosis hepatis,['hepatic peliosis'],914,,,C0030781,,,1001387,D010382,,K76.4,,
mondo:0004718,xeroderma of eyelid,,9140,,,C0155179,,,,,373.33,,,
mondo:0004719,hard palate cancer,"['malignant hard palate tumour', 'malignant tumour of the hard palate', 'malignant neoplasm of the hard palate', 'malignant tumour of hard palate', 'malignant tumor of the hard palate', 'malignant hard palate tumor', 'hard palate cancer', 'malignant tumor of hard palate', 'hard palate', 'cancer of hard palate', 'malignant neoplasm of hard palate', 'malignant hard palate neoplasm']",9149,,,C0153375,,C3528,,,145.2,C05.0,,
mondo:0004720,variola minor infection,"['whitepox', 'milkpox', 'alastrim', 'Variola minor', 'cottonpox']",9153,,,C0001906,,C34365,,,050.1,,,
mondo:0004723,liver leiomyoma,"['leiomyoma of liver', 'leiomyoma of the liver', 'hepatic leiomyoma', 'liver leiomyoma']",917,,,C1333968,,C5753,,,,,,
mondo:0004724,submandibular gland cancer,"['malignant neoplasm of submandibular gland', 'malignant tumor of submandibular gland', 'malignant tumour of submandibular gland', 'carcinoma of submandibular gland', 'malignant tumour of the submandibular gland', 'carcinoma of the submandibular gland', 'malignant tumor of the submandibular gland', 'submandibular gland carcinoma', 'malignant submandibular gland neoplasm', 'cancer of submandibular gland', 'malignant neoplasm of submaxillary gland', 'submandibular gland cancer']",9173,,,C0153360,,C8396,,,142.1,,,
mondo:0004725,rectum carcinoma in situ,"['stage 0 rectal cancer aJCC v6 and v7', 'rectal carcinoma in situ', 'stage 0 carcinoma of the rectum', 'marked rectal dysplasia', 'marked dysplasia of rectum', 'stage 0 rectal carcinoma', 'stage 0 rectum carcinoma', 'carcinoma in situ of rectum', 'rectum in situ carcinoma', 'stage 0 rectal cancer aJCC v7', 'severe dysplasia of the rectum', 'stage 0 rectal cancer', 'severe rectal dysplasia', 'marked dysplasia of the rectum', 'stage 0 carcinoma of rectum', 'carcinoma in situ of the rectum', 'stage 0 rectal cancer aJCC v6', 'severe dysplasia of rectum']",9174,,,C0154062,,C4853,,,230.4,D01.2,,
mondo:0004726,liver inflammatory myofibroblastic tumor,"['hepatic inflammatory myofibroblastic tumor', 'inflammatory pseudotumor of the liver', 'inflammatory pseudotumor of liver', 'hepatic inflammatory myofibroblastic tumour', 'liver inflammatory pseudotumor', 'liver inflammatory myofibroblastic tumor']",918,,,C1333967,,C5858,1000324,,,,,
mondo:0004727,vestibule of mouth cancer,"['malignant tumour of vestibule of mouth', 'cancer of oral opening', 'malignant oral opening neoplasm', 'malignant neoplasm of oral opening', 'malignant neoplasm of vestibule of mouth', 'malignant tumor of vestibule of mouth', 'oral opening cancer']",9188,,,C0153374,,,,,145.1,C06.1,,
mondo:0004728,diabetic macular edema,,9191,,,C0730285,,,,,362.07,,,
mondo:0004729,dyskinesia of esophagus,"['esophageal motility disorder', 'oesophageal dysmotility', 'dyskinesia of esophagus', 'esophageal dysmotility', 'oesophageal motor disorder']",9192,,,C0014858,,,1001785,D015154,530.5,K22.4,,
mondo:0004730,speech disorder,['speech impediment or impairment'],92,,,C0037822,,C5041,,D013064,784.49,,,
mondo:0004731,central sleep apnea syndrome,"['central apnea', 'hypoventilations, central alveolar', 'breathing, central sleep-disordered', 'apnea, central sleep', 'central sleep apnea', 'central sleep apnea syndrome', 'central sleep apnea, primary', 'central Apneas', 'Breathings, central sleep-disordered', 'ondine syndrome', 'central sleep-disordered breathing', 'hypoventilation, central alveolar', 'central sleep apnea, secondary', 'sleep-disordered Breathings, central', 'central sleep-disordered Breathings', 'sleep apnea, lethal central', 'sleep Apneas, central', 'central alveolar hypoventilation syndrome', 'primary central sleep apnea', 'alveolar hypoventilations, central', 'sleep disordered breathing, central', 'Apneas, central sleep', 'sleep-disordered breathing, central', 'central sleep disordered breathing', 'apnea, sleep, central', 'secondary central sleep apnea', 'central alveolar hypoventilation', 'apnea, central', 'Apneas, central', 'alveolar hypoventilation, central', 'central sleep Apneas']",9220,,,C3887547,,C27169,,D020182,327.21,,,
mondo:0004732,kidney carcinoma in situ,"['carcinoma in situ of kidney', 'stage 0 kidney carcinoma', 'kidney in situ carcinoma']",9234,,,C0686172,,,,,233.9,,,
mondo:0004733,pyriform sinus cancer,"['malignant neoplasm of pyriform sinus', 'malignant pyriform sinus tumour', 'malignant tumor of pyriform fossa', 'malignant tumor of pyriform sinus', 'malignant tumour of the pyriform fossa', 'malignant tumour of pyriform fossa', 'malignant pyriform sinus tumor', 'malignant tumor of the pyriform sinus', 'malignant pyriform fossa tumor', 'malignant tumour of pyriform sinus', 'malignant pyriform fossa tumour', 'malignant neoplasm of the pyriform sinus', 'malignant pyriform sinus neoplasm', 'malignant tumour of the pyriform sinus', 'malignant pyriform fossa neoplasm', 'malignant tumor of the pyriform fossa', 'malignant neoplasm of pyriform fossa', 'malignant neoplasm of the pyriform fossa']",9235,,,C0153400,,C3531,,,148.1,C12,,
mondo:0004736,inborn disorder of amino acid metabolism,"['inborn amino acid metabolism disorder', 'inborn error of cellular amino acid metabolic process', 'inborn errors of amino acid metabolism', 'inborn error of amino acid metabolism', 'amino acid metabolism, inborn errors', 'amino acid metabolic disorder', 'rare inborn error of cellular amino acid metabolic process']",9252,,,,,,,D000592,270.9,,,
mondo:0004737,homocystinuria,"['cystathionine beta synthase deficiency', 'cystathionine synthase deficiency', 'CBS deficiency', 'homocystinuria', 'homocystinuria (disease)']",9263,,,C0019880,,C84765,,D006712,,E72.11,,0002156
mondo:0004739,urea cycle disorder,"['inborn urea cycle disorder', 'UCD', 'disorder of metabolism of ornithine, citrulline, argininosuccinic acid, arginine and ammonia', 'disorder of urea cycle metabolism and ammonia detoxification', 'inborn disorder of urea cycle metabolism and ammonia detoxification', 'urea cycle metabolism disorder', 'disorder of urea cycle metabolism', 'urea cycle defect', 'urea cycle disorders']",9267,,79167,C0154246,,C84785,,D056806,270.6,,,
mondo:0004741,tyrosinemia,,9275,,,C0268483,,C98640,,D020176,270.2,E70.21,,
mondo:0004742,primary cerebellar degeneration,,9277,,,C0033132,,,,,334.2,,,
mondo:0004743,hyperhomocysteinemia,"['homocysteinemia', 'hyperhomocysteinemia']",9279,603174,,C3495426,,C84770,,D020138,,,,
mondo:0004744,borderline glaucoma,['Preglaucoma'],9283,,,C1533674,,,,,365.00,,,
mondo:0004745,priapism,['Mentulagra'],9286,,140949,C0033117,,,,D011317,607.3,N48.3,,
mondo:0004746,myopathy of extraocular muscle,"['myopathy of extra-ocular muscle', 'extra-ocular muscle myopathy', 'myopathy of extraocular muscles']",929,,,C0155286,,,,,376.82,,,
mondo:0004747,cleft lip,"['labium leporinum', 'cleft lip, unilateral, complete', 'hare lip', 'cleft lip (disease)', 'cleft lip', 'complete unilateral cleft lip', 'cheiloschisis']",9296,,,,,C87175,0003959,D002971,749.11,,,0410030
mondo:0004748,lip disorder,"['lip disease', 'disorder of lip', 'disease of lip', 'lip disorder', 'disease of lips', 'lip disease or disorder']",9297,,,C0023760,,C26818,,D008047,528.5,,,
mondo:0004749,myocardium cancer,"['malignant neoplasm of myocardium', 'malignant myocardial tumour', 'malignant myocardium neoplasm', 'malignant tumour of myocardium', 'malignant myocardial tumor', 'malignant tumor of myocardium', 'tumor of myocardium', 'malignant tumor of the myocardium', 'cancer of myocardium', 'malignant tumour of the myocardium', 'myocardium cancer', 'malignant myocardial neoplasm', 'tumour of myocardium', 'malignant neoplasm of the myocardium']",9299,,,C0346611,,C4569,,,,,,
mondo:0004750,language disorder,,93,,,,"['-0.1821', '0.09106', '0.2717', '-0.063', '0.01707', '-0.1614', '0.08606', '0.3347', '-0.4385', '-0.1339', '-0.03943', '-0.2101', '0.02708', '0.07776', '0.1869', '-0.2429', '-0.04153', '-0.06168', '-0.1628', '-0.5786', '-0.00901', '0.04468', '0.1043', '-0.08575', '0.1733', '-0.1733', '-0.01408', '-0.0727', '-0.2788', '-0.02188', '0.1021', '-0.007603', '0.2422', '0.0881', '-0.02467', '0.00949', '0.0268', '-0.0914', '-0.2255', '-0.2266', '0.3567', '-0.1423', '-0.0321', '0.03247', '0.065', '-0.1562', '0.0435', '-0.004406', '0.1406', '0.3284', '-0.1749', '0.1396', '-0.1483', '0.0861', '0.196', '-0.02608', '-0.02219', '-0.02226', '-0.2983', '0.2397', '0.03494', '-0.04385', '0.2094', '0.1846', '-0.03023', '0.1526', '0.0734', '0.248', '-0.2361', '0.1708', '-0.3555', '0.136', '-0.005844', '-0.09906', '0.1552', '-0.04373', '0.00766', '-0.04514', '-0.4236', '-0.0902', '0.1383', '-0.1737', '-0.04144', '0.3142', '-0.0127', '-0.03123', '0.01537', '0.0833', '0.4146', '0.2715', '0.1142', '0.4539', '-0.223', '0.05554', '0.1852', '0.2345', '0.2391', '-0.1978', '0.258', '0.234']",C97155,0005425,D007806,,,,0002463
mondo:0004751,disease of orbital part of eye adnexa,['orbital disease'],930,,,C0029182,,,,D009916,376.9,,,
mondo:0004752,neurofibroma of the heart,"['Cardiac neurofibroma', 'neurofibroma of the heart', 'heart neurofibroma', 'neurofibroma of heart']",9300,,,C1096349,,C5359,,,,,,
mondo:0004753,mechanical strabismus,,9306,,,C0152223,,,,,378.60,H50.6,,
mondo:0004754,rectal prolapse,"['rectal prolapse (disease)', 'procidentia, rectum', 'rectal prolapse']",9307,,,C0034888,,C34973,,D012005,569.1,K62.3,,0002035
mondo:0004755,monieziasis,,931,,,C0026414,,,1001372,D008989,,,,
mondo:0004756,nasal cavity neoplasm,"['nasal cavity tumor', 'nasal cavity tumour', 'tumor of nasal cavity', 'tumor of the nasal cavity', 'neoplasm of the nasal cavity', 'neoplasm of nasal cavity', 'tumour of nasal cavity', 'tumour of the nasal cavity', 'nasal cavity neoplasm (disease)', 'nasal cavity neoplasm']",9310,,,C0345630,,C4413,,,,,,
mondo:0004757,chronic ethmoidal sinusitis,"['chronic ethmoidal sinusitis', 'chronic ethmoiditis', 'ethmoidal sinusitis - chronic', 'chronic ethmoid sinusitis', 'ethmoid sinusitis, chronic']",9312,,,C0008681,,C34472,,,473.2,J32.2,,
mondo:0004758,scotoma,"['scotoma of blind spot area', 'sector or arcuate visual field defects', 'blind spot area scotoma', 'scotoma', 'scotoma (disease)', 'enlarged blind spot', 'generalized visual field contraction or constriction', 'enlarged paracaecal scotoma', 'enlarged angioscotoma', 'generalised visual field contraction or constriction']",9335,,,,,,,D012607,368.45,,,0000575
mondo:0004759,bestiality,['zoophilia'],9336,,,,,,,,302.1,,,
mondo:0004760,urethral false passage,,9339,,,,,,,,599.4,N36.5,,
mondo:0004762,Taylor syndrome,"['pelvic congestion syndrome', 'Taylor^s syndrome', 'congestion-fibrosis syndrome']",9346,,,C0152078,,,,,625.5,,,
mondo:0004763,carotid artery dissection,['dissection of carotid artery'],9348,,,C0338585,,C125662,,,443.21,I77.71,,
mondo:0004764,fibular collateral ligament bursitis,,9358,,,C0158316,,,,,726.63,,,
mondo:0004765,intrinsic asthma,,9360,,,C0155880,,,,,493.1,,,
mondo:0004766,status asthmaticus,"['asthma with status asthmaticus', 'severe asthma attack']",9362,,,C0038218,,C122577,0008590,D013224,493.91,,,
mondo:0004767,vesiculitis,"['seminal vesicles', 'seminal vesicle', 'gland, seminal vesicle', 'seminal vesicle inflammation', 'seminal vesiculitis', 'seminal Sacs']",9365,,,C0042588,,C12787,,,608.0,,,
mondo:0004768,keratoconjunctivitis,,9368,,,C0022573,,C34744,,D007637,370.8,H16.2,,0001096
mondo:0004769,orbital plasma cell granuloma,"['orbital inflammatory pseudotumor', 'orbital granuloma, plasma cell', 'pseudotumor of orbit', 'inflammatory pseudotumor, orbital', 'orbital pseudotumors', 'pseudotumor, inflammatory, orbital', 'orbital myositis', 'pseudotumors, orbital', 'inflammatory pseudotumors, orbital', 'pseudotumor, orbital inflammatory', 'inflammatory pseudotumor of orbit', 'granuloma, plasma cell, orbital', 'plasma cell granuloma, orbital', 'pseudotumor, orbital', 'orbital inflammatory pseudotumors']",9369,,,,,C117296,,D016727,376.12,,,
mondo:0004770,exophthalmos,"['proptosis', 'exophthalmos', 'exophthalmos (disease)']",9370,,,C0015300,,C118763,,D005094,376.30,,,0000520
mondo:0004772,glaucomatocyclitic crisis,"['Terrien-Viel syndrome', 'glaucomatocyclitic crisis disease', 'Posner-Schlossman syndrome']",9378,,636950,C0152138,,,,,364.22,,,
mondo:0004773,iridocyclitis,"['iridocyclitis (disease)', 'primary iridocyclitis', 'iridocyclitis']",9383,,,C0022073,,C34736,,D015863,364.3,,,0001094
mondo:0004774,gonococcal iridocyclitis,['Neisseria gonorrhoeae caused iridocyclitis (disease)'],9384,,,C0153212,,,,,098.41,A54.32,,
mondo:0004775,lens-induced iridocyclitis,['lens-induced iridocyclitis'],9388,,,C0339320,,,,,364.23,,,
mondo:0004777,acute laryngitis,"['laryngitis, acute', 'laryngitis']",9396,,,C0001327,,C26688,,,464.01,J04.0,,
mondo:0004778,epididymo-orchitis,,9401,,,C0149881,,,,,604.90,N45.3,,
mondo:0004779,epididymitis,"['epididymitis (disease)', 'epididymal', 'epididymitis', 'epididymis']",9402,,,C0014534,,C12328,,D004823,,N45.1,,0000031
mondo:0004780,strictly posterior acute myocardial infarction,,9407,,,,,,,,410.60,,,
mondo:0004781,acute myocardial infarction,"['myocardial infarction (disease), acute']",9408,,,C0155626,,C35204,0008583,,410.92,I21.9,,
mondo:0004782,diabetes insipidus,,9409,,,C0011848,,C43263,,D003919,253.5,E23.2,,
mondo:0004784,allergic asthma,"['atopic asthma', 'extrinsic asthma with acute exacerbation', 'extrinsic asthma with status asthmaticus', 'allergic form of asthma']",9415,,,C0155877,,,,,493.0,,,
mondo:0004785,blepharitis,['eyelid inflammation'],9423,,,C0005741,,C112183,,D001762,373.9,H01.0,,
mondo:0004786,chronic cholangitis,"['cholangitis, chronic']",9439,,,C0267918,,C35335,,,,,,
mondo:0004787,cervical mullerian papilloma,"['cervical Mullerian papilloma', 'cervical Müllerian papilloma', 'cervical Muellerian papilloma']",9442,,,C1516427,,C40215,,,,,,
mondo:0004788,cervix squamous papilloma,"['cervix squamous papilloma', 'squamous papilloma of cervix', 'squamous papilloma of the cervix', 'squamous papilloma of the uterine cervix', 'squamous papilloma of uterine cervix', 'squamous papilloma of the cervix uteri', 'squamous papilloma of cervix uteri', 'uterine cervix squamous papilloma', 'cervix uteri squamous papilloma', 'cervical squamous papilloma']",9445,,,C1336900,,C6342,,,,,,
mondo:0004789,cholangitis,"['biliary tree inflammation', 'biliary tract infection', 'cholangitis']",9446,,,C0008311,,C26718,,D002761,576.1,K83.0,,
mondo:0004790,fatty liver disease,"['fatty change of liver', 'steatosis of liver', 'fatty liver', 'hepatic lipidosis']",9452,,,,,,0003934,D005234,571.8,,,
mondo:0004792,cancer of isthmus of fallopian tube,"['malignant neoplasm of isthmus of fallopian tube', 'malignant isthmus of fallopian tube neoplasm', 'cancer of isthmus of fallopian tube']",9459,,,,,,,,182.1,,,
mondo:0004794,exposure keratitis,"['lagophthalmic keratitis', 'exposure keratoconjunctivitis']",9461,,,C0339295,,,,,370.34,,,
mondo:0004795,otitis externa,"['outer Ear infection', 'swimmer^s ear', 'otitis externa', 'external Ear infection', 'swimmer^s Ear', 'infectious otitis externa']",9463,,,,,C79601,,D010032,380.10,H60,,
mondo:0004796,infectious meningitis,"['infectious meningitis', 'infective meningitis', 'meningitis']",9471,,,,,C79598,0000584,,322.9,,,0001287
mondo:0004797,mononeuritis of lower limb,"['hindlimb mononeuritis simplex', 'mononeuritis simplex of hindlimb']",9473,,,,,,,,355.8,,,
mondo:0004799,ulcerative blepharitis,,9483,,,C0155173,,,,,373.01,,,
mondo:0004800,chronic dacryoadenitis,"['dacryoadenitis, chronic']",949,,,C0155224,,,,,375.02,,,
mondo:0004801,unilateral hypoactive labyrinth,,9496,,,C0155517,,,,,386.53,,,
mondo:0004802,pulmonary eosinophilia,,9498,,,C0034068,,,,D011657,518.3,,,
mondo:0004803,disseminated eosinophilic collagen disease,,9499,,,C0263662,,,,,710.8,,,
mondo:0004804,dacryoadenitis,['lacrimal gland inflammation'],950,,,C0155223,,C26971,,D003607,375.00,,,
mondo:0004805,leukocyte disorder,"['leukocyte disorder', 'disorders, leukocyte', 'disease of leukocyte', 'leukocyte disease', 'disorder, leukocyte', 'leukocyte disease or disorder', 'disorder of leukocyte']",9500,,,C0023510,,,,D007960,288.9,,,
mondo:0004806,chronic eosinophilic pneumonia,"['eosinophilic pneumonia, chronic', 'cryptogenic pulmonary eosinophilia']",9502,,,,,C34471,,,,,,
mondo:0004808,benign mammary dysplasia,,9504,,,,,,,,610.9,,,
mondo:0004810,acute ethmoiditis,"['acute ethmoidal sinusitis', 'ethmoid sinusitis, acute', 'acute ethmoid sinusitis', 'ethmoidal sinus - acute']",9506,,,C0155806,,,,,461.2,,,
mondo:0004811,simple chronic conjunctivitis,,9512,,,C0155146,,,,,372.11,,,
mondo:0004812,acute dacryoadenitis,"['dacryoadenitis, acute']",952,,,C0149505,,,,,375.01,,,
mondo:0004813,tuberculous pneumothorax,,9534,,,C0152600,,,,,011.76,,,
mondo:0004815,osteosclerotic plasma cell myeloma,"['osteosclerotic myeloma', 'osteosclerotic multiple myeloma', 'osteosclerotic plasma cell myeloma']",9541,,,,,C7765,,,,,,
mondo:0004816,refractory plasma cell neoplasm,['refractory plasma cell neoplasm'],9544,,,C0278620,,C7813,,,,,,
mondo:0004817,non-secretory plasma cell myeloma,"['non-secretory plasma cell myeloma', 'non-secretory myeloma', 'non-secretory multiple myeloma']",9547,,,C3898125,,C4734,,,,,,
mondo:0004819,indolent plasma cell myeloma,"['indolent plasma cell myeloma', 'indolent myeloma']",9550,,,C2049069,,C7150,,,,,,
mondo:0004820,peripheral nerve schwannoma,['peripheral nerve schwannoma'],956,,,C1519001,,C41430,,,,,,
mondo:0004821,nasopharyngeal disorder,"['nasopharynx disease or disorder', 'nasopharynx disease', 'nasopharyngeal disorder', 'disorder of nasopharynx', 'disease of nasopharynx']",9561,,,C0027438,,C35723,,D009302,,,,
mondo:0004822,bronchiectasis,['Polynesian bronchiectasis'],9563,,,C0006267,,C84475,,D001987,494,J47,,
mondo:0004824,neonatal candidiasis,"['neonatal Monilia infection', 'neonatal candida infection', 'neonatal moniliasis', 'neonatal Candida infection']",9577,,,C0276682,,C116810,,,771.7,P37.5,,
mondo:0004826,urethral calculus,"['urolithiasis of urethra', 'urethra urolithiasis', 'urethral Stone']",9589,,,C0162301,,,,,594.2,,,
mondo:0004827,esophagus squamous cell papilloma,"['squamous cell papilloma of the esophagus', 'squamous cell papilloma of oesophagus', 'squamous cell papilloma of esophagus', 'esophagus squamous papilloma', 'squamous cell papilloma of the oesophagus', 'esophagus squamous cell papilloma', 'oesophagus squamous papilloma', 'esophageal squamous papilloma']",959,,,C1333467,,C5344,,,,,,
mondo:0004828,lower urinary tract calculus,"['lower urinary tract urolithiasis', 'urolithiasis of lower urinary tract']",9590,,,C0156264,,,,,594.9,N21.9,,
mondo:0004829,Krukenberg carcinoma,"['Krukenberg tumour', 'Krukenberg’s tumour', 'Krukenberg’s tumor', 'Krukenberg neoplasm', 'Krukenberg tumor']",9597,,,C0022790,,C3153,1000316,D007725,,,,
mondo:0004830,fasciitis,"['fasciitis (disease)', 'fascia inflammation', 'fasciitis', 'Fascitis']",9598,,,C0015645,,C50559,,D005208,729.4,,,0100537
mondo:0004831,proliferative fasciitis,,9599,,,C0432528,,C4728,,,,,,
mondo:0004832,esophagus leiomyoma,"['leiomyoma of the esophagus', 'leiomyoma of esophagus', 'leiomyoma of the oesophagus', 'esophageal leiomyoma', 'esophagus leiomyoma', 'leiomyoma of oesophagus']",960,,,C0238114,,C3866,,,,,,
mondo:0004833,plantar fasciitis,,9600,,,C0149756,,,1001909,D036981,,,,
mondo:0004834,ischemic fasciitis,['atypical decubital fibroplasia'],9601,,,C1304514,,C6483,,,,,,
mondo:0004835,necrotizing fasciitis,,9602,,,C0238124,,C84916,,D019115,728.86,M72.6,,
mondo:0004836,intravascular fasciitis,"['intravascular pseudosarcomatous fasciitis', 'intravascular nodular fasciitis']",9603,,,C0432529,,C4729,,,728.79,,,
mondo:0004837,neurofibroma of the esophagus,"['neurofibroma of the esophagus', 'esophageal neurofibroma', 'esophagus neurofibroma', 'oesophagus neurofibroma', 'neurofibroma of esophagus', 'neurofibroma of oesophagus']",961,,,C1333463,,C5704,,,,,,
mondo:0004838,orthostatic proteinuria,['postural albuminuria'],9617,,,C0232867,,,,,593.6,,,
mondo:0004840,non-congenital cyst of kidney,,9621,,,C0268799,,,,,593.2,,,
mondo:0004841,kidney hypertrophy,"['renal Hypertrophy', 'hypertrophy of the kidney']",9622,,,C0156259,,C122991,,,593.1,N28.81,,
mondo:0004842,stomatitis,"['mouth mucosa inflammation', 'oral mucositis', 'mucositis oral']",9637,,,C1568868,,C26887,1001904,D013280,528.00,,,
mondo:0004843,pathologic nystagmus,,9650,,,C0028738,,,,D009759,379.50,,,
mondo:0004844,oral mucosa leukoplakia,"['oral keratoses', 'leukoplakia of the oral mucosa', 'leukoplakia of oral mucosa', 'oral leukoplakia', 'oral keratosis', 'leukokeratosis of oral mucosa']",9655,,,C0023532,,C3187,,D007972,528.6,,,
mondo:0004845,aphthous stomatitis,"['aphthous ulceration', 'oral aphthous ulcer', 'aphtha', 'oral aphthae', 'oral ulcer', 'canker sore']",9663,,,,,,,,528.2,,,
mondo:0004846,placental abruption,"['premature separation of placenta', 'abruptio placentae', 'Abruptio placentae, premature separation of placenta', 'abruptio placenta', 'placental abruption', 'placental abruption (disease)']",9667,,,,,C26685,1001754,D000037,641.20,,,0011419
mondo:0004847,senile cataract,,9669,,,,,C35012,,,366.10,,,
mondo:0004848,ulcerative stomatitis,['ulcerative stomatitis'],9673,,,C0038367,,C35039,,D005892,528.00,,,
mondo:0004849,pulmonary emphysema,"['emphysema, pulmonary', 'emphysema']",9675,,,,,C3348,0000464,D011656,492.8,J43,,
mondo:0004851,toxic myocarditis,,9694,,,C0155691,,,,,422.93,,,
mondo:0004852,gonococcal keratitis,,9697,,,C0153214,,,,,098.43,A54.33,,
mondo:0004853,gonococcal endophthalmia,,9698,,,C0153213,,,,,098.42,,,
mondo:0004854,ophthalmia neonatorum,"['gonococcal ophthalmia neonatorum', 'neonatal conjunctivitis', 'gonococcal conjunctivitis (neonatorum)']",9699,,,C0029076,,C116815,,D009878,771.6,,,
mondo:0004855,tenosynovitis,"['tendon sheath inflammation', 'Inflammation of tendon sheath', 'Tenosynovitides']",970,,,C0039520,,,1001435,D013717,,,,
mondo:0004856,rosacea conjunctivitis,,9709,,,C0155152,,,,,372.31,,,
mondo:0004857,tendinitis,"['tendon inflammation', 'tendonitis']",971,,,C0039503,,C97141,,,,,,
mondo:0004858,occlusion of gallbladder,['obstruction of gallbladder'],9714,,,C0156214,,,,,575.2,K82.0,,
mondo:0004859,hydrops of gallbladder,,9717,,,C0152445,,,,,575.3,K82.1,,
mondo:0004860,vitreous disorder,"['disease of vitreous humor', 'disorder of vitreous humour', 'disease or disorder of vitreous humour', 'disorder of vitreous humor', 'vitreous humor disease', 'vitreous humour disease or disorder', 'disease of vitreous humour', 'vitreous humor disease or disorder', 'vitreous humour disease']",9720,,,,,,,,379.24,,,
mondo:0004861,ophthalmia nodosa,,9722,,,C0154775,,,,,360.14,,,
mondo:0004862,vitreous abscess,,9723,,,C0042904,,,,,360.04,,,
mondo:0004863,purulent endophthalmitis,,9724,,,C0259800,,,,,360.00,H44.0,,
mondo:0004864,acute allergic mucoid otitis media,,9735,,,C0155419,,,,,381.05,,,
mondo:0004865,blue drum syndrome,['acute mucoid otitis media'],9736,,,C0395863,,,,,381.02,,,
mondo:0004866,eustachian tube disorder,"['disease of pharyngotympanic tube', 'pharyngotympanic tube disease or disorder', 'pharyngotympanic tube disease', 'disorder of pharyngotympanic tube']",9739,,,C0271468,,,,,381.9,H68,,
mondo:0004867,upper respiratory tract disorder,"['upper respiratory tract disease or disorder', 'disorder of upper respiratory tract', 'upper respiratory tract disease', 'disease of upper respiratory tract']",974,,,,,,,,478.9,,,
mondo:0004868,biliary tract disorder,"['biliary tree disease or disorder', 'biliary tree disease', 'disorder of biliary tree', 'disease of biliary tree']",9741,,,,,,,D001660,576.9,,,
mondo:0004869,pelvic varices,"['pelvic region of trunk varicose disease', 'varicose disease of pelvic region of trunk']",9742,,,C0155795,,,,,456.5,I86.2,,
mondo:0004871,perianal hematoma,"['Thrombosed external haemorrhoids', 'external thrombosed haemorrhoids', 'Thrombosed external hemorrhoids', 'external thrombosed hemorrhoids']",9745,,,,,,,,455.4,,,
mondo:0004872,hemorrhoid,"['Hemorrhoids', 'hemorrhoidal disease', 'Haemorrhoids', 'hemorrhoid']",9746,,,C0019112,,C26792,,D006484,455.8,,,
mondo:0004873,internal hemorrhoid,['internal hemorrhoid'],9749,,,C0265034,,C35319,,,455.6,,,
mondo:0004874,ganglion or cyst of synovium/tendon/bursa,,9754,,,,,,,,727.49,,,
mondo:0004875,xanthogranulomatous cholecystitis,['CX'],9766,,,C1337035,,C35792,,C536762,,,,
mondo:0004876,myocardial stunning,,9767,,,C0206146,,,,D017682,,,,
mondo:0004877,transient neonatal thrombocytopenia,,9771,,,C0158991,,,,,776.1,P61.0,,
mondo:0004878,female breast upper-outer quadrant cancer,,9773,,,C0153552,,,,,174.4,,,
mondo:0004879,senile atrophy of choroid,,9776,,,C0154891,,,,,363.41,,,
mondo:0004880,bowel dysfunction,"['disease of lower digestive tract', 'lower digestive tract disease']",9779,,,C2004461,,,,,564.9,,,
mondo:0004881,myositis fibrosa,['interstitial myositis'],9788,,,C0158362,,C26985,,,728.81,M60.1,,
mondo:0004882,angioid streaks of choroid,"['angioid streaks of optic choroid', 'optic choroid angioid streaks']",979,,,C0002983,,,,,363.43,,,
mondo:0004883,hereditary choroidal atrophy,,9794,,,C0154893,,,,,363.50,,,
mondo:0004884,eye degenerative disorder,"['neurodegenerative disease of eyeball of camera-type eye', 'eye neurodegenerative disease', 'eyeball of camera-type eye neurodegenerative disease']",9799,,,C0154777,,,,,360.40,H44.5,,
mondo:0004885,choroidal sclerosis,"['optic choroid neurodegenerative disease', 'choroidal degenerations', 'neurodegenerative disease of optic choroid']",980,,,,,,,C535358,363.40,,,
mondo:0004886,diffuse secondary choroid atrophy,,981,,,C0154892,,,,,363.42,,,
mondo:0004888,partial circumpapillary choroid dystrophy,,9811,,,C0154895,,,,,363.51,,,
mondo:0004889,total central choroidal atrophy,"['choroidal dystrophy, serpiginous']",9820,,,C0154898,,,,,363.54,,,
mondo:0004890,partial central choroid dystrophy,"['choroidal dystrophy, central areolar']",9822,,,C0339427,,,,,363.53,,,
mondo:0004891,hyperopia,"['hypermetropia', 'Far-sightedness']",9834,,,C0020490,,,,D006956,367.0,H52.0,,
mondo:0004892,refractive error,,9835,,,,,,,D012030,,,,
mondo:0004893,hypertropia,,9837,,,C0020575,,C34716,,,378.31,,,
mondo:0004894,cyclotropia,,9838,,,C0152209,,,,,378.33,,,
mondo:0004895,accommodative esotropia,,9839,,,C0155336,,,,,378.35,,,
mondo:0004896,esotropia,"['convergence in manifest squint', 'internal strabismus', 'crossed eyes']",9840,,,C0014877,,C34596,,D004948,378.00,,,
mondo:0004897,hypotropia,"['sunset sign', 'downward ocular deviation', 'hypotropia']",9841,,,C0152208,,C42086,,,378.32,,,
mondo:0004898,total circumpapillary dystrophy of choroid,"['circumpapillary dystrophy of choroid, total']",9842,,,C0154896,,,,,363.52,,,
mondo:0004899,monofixation syndrome,"['microstrabismus', 'microtropia']",9843,,,C0339611,,,,,378.34,H50.42,,
mondo:0004900,peripheral vertigo,,9847,,,C0155501,,,,,386.19,,,
mondo:0004901,lingual-facial-buccal dyskinesia,['oro-facial dyskinesia'],9854,,,C0152115,,,,,333.82,,,
mondo:0004902,interstitial keratitis,,9857,,,C0155088,,,,,370.50,,,
mondo:0004903,deep keratitis,,9858,,,C2960633,,,,,370.59,,,
mondo:0004904,toxic maculopathy,['toxic maculopathy of retina'],9867,,,C0271086,,,,,362.55,,,
mondo:0004905,intestinal disaccharidase deficiency,['intestinal disaccharidase deficiency and disaccharide malabsorption'],9868,,,,,C34731,1000060,,271.3,,,
mondo:0004907,alopecia,"['alopecia areata', 'hair loss', 'loss Of hair', 'alopecia']",987,,79364,C0002170,,C50575,,D000505,704.09,,,
mondo:0004909,urethral gland abscess,,9877,,,,,,,,597.0,,,
mondo:0004910,mitral valve prolapse,"['mitral valve prolapse', 'myxomatous mitral valve prolapse', 'barlow^s syndrome', 'mitral valve prolapse (disease)', 'floppy mitral valve', 'mitral valve prolapse, myxomatous', 'systolic click-murmur syndrome', 'valve, prolapse Of mitral', 'mitral leaflet syndrome', 'mitral valve prolapse syndrome', 'prolapse, mitral valve']",988,,,,,C50655,,D008945,,,,0001634
mondo:0004911,cardiovascular syphilis,,9880,,,C0039130,,,,,093.9,,,
mondo:0004913,alternating esotropia,,9888,,,C0152205,,,,,378.05,H50.05,,
mondo:0004914,celiac artery stenosis from compression by median arcuate ligament of diaphragm,"['syndromic disease of median arcuate ligament', 'Harjola-Marable syndrome', 'celiac access syndrome', 'median arcuate ligament syndromic disease', 'Marable^s syndrome', 'coeliac access syndrome', 'median arcuate ligament syndrome', 'celiac artery stenosis from compression by median arcuate ligament of diaphragm', 'celiac artery compression syndrome', 'coeliac artery compression syndrome']",9892,116870,,C1861783,,,,C566151,447.4,,,
mondo:0004917,internal hordeolum,"['hordeolum of tarsal gland', 'tarsal gland hordeolum']",9908,,,C0085690,,,,,373.12,,,
mondo:0004918,central corneal ulcer,,9910,,,C0155069,,,,,370.03,,,
mondo:0004919,infected hydrocele,,9911,,,C0156300,,,,,603.1,N43.1,,
mondo:0004920,hydrocele,,9912,,,,,,,,603.9,,,
mondo:0004922,developmental coordination disorder,"['clumsy child syndrome', 'developmental dyspraxia', 'development coordination disorder']",9923,,,C0520947,,C92561,,D019957,315.4,,,
mondo:0004923,chronic inflammation of lacrimal passage,,9935,,,C0155239,,,,,375.4,,,
mondo:0004924,chronic canaliculitis,"['chronic actinomycosis', 'actinomycosis, chronic']",9936,,,C0155240,,,,,375.41,,,
mondo:0004925,chronic dacryocystitis,"['dacryocystitis, chronic']",9937,,,C0149506,,,,,375.42,,,
mondo:0004926,dacryocystitis,"['dacryoadenitis', 'lacrimal sac inflammation', 'Dacryocystitides', 'Dacryoadenitides']",9938,,,C0010930,,C34521,,D003607,375.30,,,
mondo:0004927,dacryocystocele,['lacrimal mucocele'],9939,,,,,,,,375.43,,,
mondo:0004928,lymph node disorder,"['lymph node disease or disorder', 'lymph node disorder', 'lymph node disease', 'disease of lymph node', 'disorder of lymph node']",9942,,,C0272394,,C35346,,,,,,
mondo:0004929,constant exophthalmos,,9945,,,C0155267,,,,,376.31,,,
mondo:0004930,steroid-induced glaucoma,['corticosteroid-induced glaucoma'],9946,,,C0339578,,,,,365.89,,,
mondo:0004931,residual stage corticosteroid-induced glaucoma,,9948,,,C0339580,,,,,365.32,,,
mondo:0004932,null-cell leukemia,"['null cell acute lymphoblastic leukaemia', 'null cell acute lymphoblastic leukemia']",9954,,,C0023483,,,,,,,,
mondo:0004933,hypoplastic left heart syndrome,['HLHS'],9955,,2248,C0152101,,C98894,,D018636,746.7,Q23.4,10021076,
mondo:0004934,periostitis,"['periosteum inflammation', 'periostitis', 'periosteum', 'periostitis (disease)']",9957,,,C0031111,,C13184,,D010522,,,,0040165
mondo:0004936,uterine inversion,,997,,,,,,1001446,D019687,665.2,,,
mondo:0004937,hypervitaminosis D,['hypervitaminosis type D'],9971,,,C1442839,,,,,278.4,E67.3,,
mondo:0004938,substance dependence,['dependence'],9973,,,,,C35458,,,304.60,,,
mondo:0004939,hallucinogen dependence,,9977,,,,,C34657,,,304.50,,,
mondo:0004940,acute female pelvic peritonitis,,9978,,,C0269032,,,,,614.5,N73.3,,
mondo:0004941,eosinophilia-myalgia syndrome,"['severe muscle pain and abnormally high eosinophils', 'syndrome with inflammatory and autoimmune components that affect the skin, fascia, muscle, nerve, blood vessels, lung, and heart', 'eosinophilia myalgia syndrome', 'EMS', 'L-tryptophan induced EMS']",998,,,,,,1001316,D016603,710.5,,,
mondo:0004942,orbit lymphoma,"['lymphoma of the orbit', 'lymphoma of orbit', 'primary orbit lymphoma', 'primary orbital lymphoma', 'orbital lymphoma']",9986,,,C0271333,,C6244,,C537131,,,,
mondo:0004943,orbit sarcoma,"['orbit of skull sarcoma', 'orbital sarcoma', 'sarcoma of orbit', 'sarcoma of orbit of skull', 'sarcoma of the orbit']",9987,,,C1335131,,C6095,,,,,,
mondo:0004944,neurosyphilis,"['neurosyphilis', 'late neurosyphilis', 'tertiary neurosyphilis']",9988,,,C0027927,,C84935,,D009494,094.9,A52.3,,
mondo:0004946,hypoglycemia,"['low blood glucose', 'blood glucose, Low', 'hypoglycaemia', 'glucose, Low blood']",9993,,,C0020615,,C3126,,D007003,251.2,,,
mondo:0004947,B-cell acute lymphoblastic leukemia,"['precursor B-lymphoblastic lymphoma/leukemia', 'B lymphoblastic leukemia/lymphoma', 'precursor B lymphoblastic leukemia/lymphoma', 'precursor B lymphoblastic lymphoma/leukemia']",7061,,,,,C8936,0000094,,,,,
mondo:0004948,B-cell chronic lymphocytic leukemia,"['B-cell chronic lymphoid leukemia', 'B-cell chronic lymphogenous leukaemia', 'B cell lymphocytic leukemia', 'chronic lymphatic leukemia', 'chronic B-cell lymphocytic leukaemia', 'small lymphocytic lymphoma', 'chronic lymphogenous leukaemia', 'leukemia, lymphocytic, chronic', 'B-cell chronic lymphogenous leukemia', 'B-cell lymphocytic leukaemia', 'chronic B-cell lymphocytic leukemia', 'B-CLL', 'chronic lymphocytic leukaemia (CLL)', 'chronic lymphocytic leukaemia', 'chronic lymphogenous leukemia', 'chronic lymphatic leukaemia', 'B cell chronic lymphocytic leukaemia', 'BCLL', 'B cell CLL', 'B-cell chronic lymphoid leukaemia', 'CLL', 'hematopoeitic - chronic lymphocytic leukaemia (CLL)', 'B cell chronic lymphocytic leukemia', 'B cell lymphocytic leukaemia', 'chronic lymphocytic leukemia (CLL)', 'B-cell CLL', 'leukemia, chronic lymphatic', 'B-cell lymphocytic leukemia', 'lymphoplasmacytic leukemia', 'lymphoplasmacytic leukaemia', 'B-cell chronic lymphocytic leukemia', 'leukemia, chronic LYMPHOCYTIC', 'hematopoeitic - chronic lymphocytic leukemia (CLL)', 'chronic lymphocytic leukemia']",1040,151400,67038,C0855095,"['0.01292', '0.3306', '-0.1057', '0.1277', '0.0793', '-0.1952', '0.555', '0.7427', '-0.2279', '-0.7056', '0.5557', '0.4233', '-0.4626', '0.3667', '-0.267', '-0.2246', '-0.722', '-0.244', '-0.4248', '-0.572', '-0.344', '0.1958', '0.4536', '-0.1142', '0.4976', '0.1556', '-0.07043', '-0.07916', '-0.4722', '-0.2363', '0.485', '0.1368', '0.563', '0.10425', '0.429', '0.0651', '-1.567', '0.36', '-0.2231', '-0.4143', '-0.1925', '0.2396', '0.1503', '-0.926', '0.1527', '0.09125', '-0.3809', '-0.6895', '0.5923', '0.2727', '0.2737', '0.2462', '-0.1968', '0.2654', '0.2136', '0.1372', '-0.7793', '-0.3887', '-0.06192', '-0.471', '0.4512', '0.2358', '-0.1254', '-0.2079', '-0.002274', '-0.0872', '0.4304', '0.4146', '0.144', '1.309', '0.0466', '-0.2048', '0.1179', '0.2979', '0.3699', '0.0976', '0.1886', '0.3665', '0.1326', '-0.3362', '-0.445', '-0.537', '0.3079', '-0.409', '-0.2255', '-0.3447', '0.8516', '-0.04428', '0.6855', '-0.257', '0.2578', '0.0324', '-0.104', '0.084', '0.851', '0.9893', '-0.1487', '0.0742', '0.02911', '-0.2856']",C3163,0000095,D015451,204.1,,10008958,
mondo:0004949,neoplasm of mature B-cells,"['mature B-cell lymphocytic neoplasm', 'mature B-cell neoplasms', 'mature B-cell neoplasm']",706,,,C1334633,,C3457,0000096,,202.0,,,
mondo:0004950,gastric carcinoma,"['fundus of stomach cancer', 'gastric cancer, NOS', 'carcinoma of the stomach', 'gastric carcinoma', 'stomach cancer', 'cancer of stomach', 'malignant fundus of stomach neoplasm', 'malignant tumour of fundus of stomach', 'Ca fundus - stomach', 'gastric (stomach) cancer', 'carcinoma of stomach', 'malignant tumor of fundus of stomach', 'gastric cancer', 'cancer of the stomach', 'cancer of fundus of stomach', 'malignant neoplasm of fundus of stomach', 'gastric fundus cancer', 'stomach carcinoma']",5517,,,C0699791,"['-0.1159', '0.1315', '-0.007626', '0.0473', '0.04272', '-0.06934', '0.0465', '0.09155', '-0.05957', '-0.03314', '-0.05508', '-0.06824', '-0.1162', '0.10645', '-0.2566', '-0.1647', '-0.0393', '-0.1345', '0.0898', '-0.2463', '-0.015236', '-0.1545', '0.1305', '-0.1896', '0.1748', '-0.06433', '0.02095', '0.03302', '-0.0859', '-0.1749', '0.1936', '-0.00205', '0.1207', '-0.09015', '0.0009427', '0.00848', '-0.0898', '0.03903', '0.02675', '-0.11414', '-0.013176', '-0.2399', '0.0515', '-0.1356', '-0.0687', '-0.04526', '-0.0573', '0.011284', '0.11334', '0.02538', '0.01971', '0.02538', '0.10095', '0.06744', '-0.2036', '-0.05737', '0.11694', '0.03262', '-0.3027', '-0.0122', '0.1512', '0.0748', '-0.03912', '0.01005', '0.0452', '0.10767', '0.2878', '0.2013', '-0.2017', '0.1693', '0.02583', '-0.007565', '0.1103', '-0.08075', '0.0836', '0.08716', '-0.01572', '-0.0189', '-0.00543', '-0.1664', '-0.258', '0.0809', '-0.07666', '-0.01021', '-0.1523', '-0.075', '0.05148', '0.07886', '0.2522', '-0.1342', '-0.004265', '0.2012', '0.03943', '-0.01689', '0.3108', '0.00783', '0.135', '-0.2517', '-0.1301', '0.07355']",C4911,0000178,,230.2,,,
mondo:0004951,susceptibility to HIV infection,"['HIV-1 disease, delayed progression of', 'HIV-1, susceptibility to', 'AIDS, resistance to', 'acquired immunodeficiency syndrome, progression to', 'HIV/AIDS, susceptibility to', 'AIDS, progression to', 'human immunodeficiency virus type 1, susceptibility to', 'HIV-1 viremia, susceptibility to', 'HIV-1 disease, rapid progression of', 'HIV type 1, susceptibility to', 'AIDS, slow progression to', 'rapid progression to AIDS from HIV1 infection', 'AIDS, delayed/rapid progression to', 'HIV-1, resistance to', 'human immunodeficiency virus type 1, resistance to', 'HIV1 infection, resistance to', 'AIDS, rapid progression to', 'HIV infection, resistance to', 'HIV1, resistance to']",,609423,,CN282826,"['-0.002922', '0.013885', '0.01158', '-0.0365', '0.0088', '-0.07526', '0.03952', '0.015114', '-0.0314', '-0.0898', '0.00729', '0.00604', '-0.03195', '0.04126', '-0.02002', '-0.03293', '-0.03918', '-0.02931', '-0.0439', '-0.1041', '0.01276', '-0.03094', '0.0741', '-0.02379', '0.013954', '-0.01596', '-0.01355', '0.0398', '-0.01854', '-0.0506', '0.0555', '0.007378', '0.0307', '-0.007656', '0.02045', '0.01475', '-0.02678', '-0.02344', '-0.003527', '-0.05637', '0.01012', '-0.02759', '0.0236', '-0.02019', '-0.0136', '-0.07684', '-0.0013485', '0.03897', '0.006294', '0.02827', '-0.05856', '-0.02133', '0.04715', '0.00882', '-0.01913', '-0.01185', '0.0817', '-0.03017', '-0.0843', '0.01354', '0.01581', '0.03632', '-0.002546', '0.04395', '0.03302', '0.03568', '0.06192', '0.0653', '-0.07', '0.1229', '-0.0706', '-0.01108', '0.02306', '-0.0515', '0.04425', '0.02963', '0.011635', '0.005486', '0.00701', '-0.01297', '-0.0712', '-0.04926', '-0.004066', '0.05493', '-0.03091', '0.002567', '0.02289', '0.0288', '0.0711', '0.03105', '0.03824', '0.06647', '-0.02701', '0.01513', '0.11896', '0.0897', '0.0682', '-0.06192', '-0.02536', '-0.02254']",C14220,0000180,,,,,
mondo:0004952,Hodgkins lymphoma,"['lymphoma, Hodgkin^s', 'stage II subdiaphragmatic Hodgkin lymphoma', 'Hodgkin^s lymphoma', 'Hodgkin^s sarcoma', 'stage I subdiaphragmatic Hodgkin lymphoma', 'Hodgkin disease', 'Hodgkin^s disease', 'Hodgkin lymphoma', 'Hodgkins lymphoma', 'HL']",8567,,98293,,"['0.2903', '0.2195', '0.2399', '-0.5264', '0.10925', '-0.1854', '0.5205', '1.024', '-0.2576', '-0.525', '0.2213', '0.4458', '-0.4568', '-0.02031', '0.1493', '-0.1685', '-0.7827', '-0.5107', '-0.3152', '-0.1826', '-0.3022', '0.2179', '0.4368', '-0.1661', '0.2222', '0.3762', '-0.2046', '0.02634', '-0.688', '-0.2559', '0.697', '0.649', '0.4707', '-0.4033', '0.337', '0.0905', '-1.357', '0.3232', '-0.3967', '-0.2462', '0.0373', '-0.2754', '0.1869', '-0.84', '0.6816', '0.2177', '-0.858', '-0.31', '0.7656', '0.2615', '0.47', '-0.1071', '0.0892', '0.1873', '-0.331', '0.2734', '-0.1577', '-0.06885', '-0.1361', '-0.4893', '0.2358', '0.3328', '-0.1284', '-0.251', '-0.2827', '0.2129', '0.1864', '0.51', '-0.01191', '1.166', '-0.0246', '0.1678', '-0.1814', '-0.2137', '0.6323', '0.0723', '0.03137', '0.315', '-0.06915', '-0.552', '-0.3213', '-0.4568', '0.06995', '-0.00209', '-0.1584', '-0.678', '0.4285', '-0.3276', '0.2642', '-0.3064', '0.8525', '-0.3037', '0.1412', '-0.03085', '0.8755', '0.4775', '-0.02245', '-0.0795', '-0.5913', '-0.4678']",C9357,0000183,D006689,201.90,,,
mondo:0004953,invasive ductal breast carcinoma,"['invasive ductal carcinoma of the breast', 'invasive ductal carcinoma, NST', 'infiltrating ductal breast carcinoma', 'invasive ductal carcinoma of breast', 'breast invasive ductal carcinoma', 'invasive ductal adenocarcinoma', 'invasive ductal breast carcinoma', 'infiltrating ductal carcinoma of breast', 'infiltrating ductal carcinoma of the breast', 'infiltrating ductal adenocarcinoma', 'ductal adenocarcinoma', 'invasive ductal carcinoma', 'invasive ductal carcinoma, No specific type', 'infiltrating ductal carcinoma']",3008,,,,,C4194,0000186,,174.8,,,
mondo:0004956,metastatic prostate carcinoma,"['prostate carcinoma metastatic', 'prostate cancer metastatic', 'metastatic prostate carcinoma', 'metastatic prostate cancer']",,,,,,C8946,0000196,,199.1,,,
mondo:0004957,mucinous adenocarcinoma,"['gelatinous adenocarcinoma', 'colloid adenocarcinoma', 'mucin-secreting carcinoma', 'mucinous carcinoma', 'mucoid carcinoma', 'mucin-secreting adenocarcinoma', 'mucin-producing adenocarcinoma', 'pseudomyxoma peritonei with unknown primary site', 'mucinuos carcinoma', 'gelatinous carcinoma', 'mucinous adenocarcinoma', 'adenocarcinoma, mucinous, malignant', 'mucoid adenocarcinoma', 'mucous adenocarcinoma', 'mucous carcinoma', 'mucin-producing adenocarcinoma (morphologic abnormality)', 'CEMU', 'colloid carcinoma']",3030,,,C0334368,,C26712,0000197,D002288,,,,
mondo:0004958,oral cavity squamous cell carcinoma,"['scc of the oral cavity', 'squamous cell carcinoma of the oral cavity', 'OCSC', 'scc of oral cavity', 'squamous cell carcinoma of oral cavity', 'scc of the mouth', 'mouth squamous cell carcinoma', 'scc of mouth', 'squamous cell carcinoma of the mouth', 'oral squamous cell carcinoma', 'oral cavity scc', 'squamous cell carcinoma of mouth', 'oral cavity squamous cell carcinoma', 'mouth scc', 'oral cavity squamous cell cancer']",0050866,,502363,C0585362,,C4833,0000199,,,,,
mondo:0004959,plasma cell neoplasm,"['plasma cell tumor', 'plasma cell neoplasm', 'plasma cell tumour', 'plasmacytic tumour', 'plasma cell tumor, malignant', 'plasmacytic neoplasm', 'plasmacytic tumor', 'plasma cell dyscrasia']",6536,,98282,C1959632,,C4665,0000200,D054219,238.6,,,
mondo:0004960,monoclonal gammopathy,,,,,,,C35548,0000203,D010265,,D47.2,,
mondo:0004961,stage I endometrioid carcinoma,,,,,,,,0000205,,,,,
mondo:0004962,stage II endometrioid carcinoma,,,,,,,,0000206,,,,,
mondo:0004963,T-cell acute lymphoblastic leukemia,"['acute T-cell lymphoblastic leukaemia', 'T-cell ALL', 'precursor T-lymphoblastic leukemia', 'acute T cell leukemia', 'T-cell type acute leukaemia', 'acute T-cell leukemia', 'T-cell acute lymphoblastic leukemia', 'T-cell type acute leukemia', 'precursor T-lymphoblastic leukaemia', 'T acute lymphoblastic leukemia', 'acute T-cell leukaemia', 'acute T-cell lymphoblastic leukemia', 'acute T-cell lymphocytic leukaemia', 'T-cell acute lymphocytic leukaemia', 'acute T-cell lymphocytic leukemia', 'acute T cell lymphoblastic leukaemia', 'acute T cell lymphocytic leukaemia', 'T-ALL', 'T-cell acute lymphocytic leukemia', 'acute T cell leukaemia', 'precursor T-lymphoblastic leukaemia (T-cell ALL)', 'T acute lymphoblastic leukaemia', 'acute T cell lymphoblastic leukemia', 'precursor T-lymphoblastic leukemia (T-cell ALL)', 'acute T cell lymphocytic leukemia']",5603,,,,,C3183,0000209,,,,,
mondo:0004964,"peripheral T-cell lymphoma, not otherwise specified","['PTCL', 'peripheral T-cell lymphoma, not otherwise specified']",,,,,,C4340,0000211,,,,,
mondo:0004965,acinar cell carcinoma,"['acinic cell tumour', 'carcinoma of acinar cell', 'acinar cell adenocarcinoma', 'acinic cell tumor', 'acinar cell carcinoma', 'acinar adenocarcinoma', 'acinic cell adenocarcinoma', 'acinic cell carcinoma', 'acinar cell carcinoma (morphologic abnormality)', 'carcinoma, acinar cell, malignant', 'acinar carcinoma', 'ACCC']",3025,,,C0206685,,C3768,0000216,D018267,,,,
mondo:0004966,gastritis,"['gastritis', 'stomach inflammation', 'erosive gastritis', 'erosive gastropathy', 'acute gastric mucosal erosion', 'gastritis (disease)']",4029,,,C3854048,,C26780,0000217,D005756,535.41,,,0005263
mondo:0004967,acute lymphoblastic leukemia,"['precursor cell lymphoblastic leukaemia', 'acute lymphoblastic leukemia (ALL)', 'acute lymphogenous leukaemia', 'acute lymphoblastic leukaemia (ALL)', 'acute lymphoblastic leukaemia (disease)', 'acute lymphoid leukaemia', 'acute lymphoblastic leukemia', 'ALL - acute lymphocytic leukemia', 'precursor cell lymphoblastic leukemia', 'ALL', 'acute lymphoid leukemia', 'acute lymphocytic leukaemia', 'leukemia, lymphoblastic, malignant', 'precursor lymphoblastic leukaemia', 'lymphoblastic leukaemia', 'precursor Lymphoblasic leukaemia', 'acute lymphogenous leukemia', 'lymphoblastic leukemia, acute', 'acute lymphoblastic leukemia/lymphoma', 'acute lymphocytic leukemia', 'acute lymphoblastic leukemia (disease)', 'ALL - acute lymphocytic leukaemia', 'lymphoblastic leukemia', 'precursor lymphoblastic leukemia', 'precursor Lymphoblasic leukemia', 'acute lymphocytic leukemias']",9952,,513,,"['0.271', '-0.379', '0.0422', '0.3462', '-0.4202', '0.007675', '0.3853', '1.408', '-0.1885', '-0.5605', '0.2883', '0.2158', '-0.1562', '0.4426', '0.04807', '0.1366', '-0.6284', '-0.695', '-0.00948', '-0.2338', '-0.652', '-0.4248', '0.5503', '-0.2993', '0.0884', '-0.05032', '0.5264', '-0.144', '-0.635', '0.03128', '0.909', '0.9277', '0.873', '-0.1644', '0.1288', '0.5903', '-0.9663', '0.4338', '0.239', '-0.4104', '-0.2192', '-0.1595', '0.3198', '-0.336', '-0.4395', '0.1954', '-0.07697', '-0.7', '0.11304', '0.1827', '0.512', '0.0807', '0.6074', '0.5327', '-0.2126', '-0.2368', '-0.2473', '0.4058', '-0.8647', '-0.4548', '0.01875', '0.6753', '0.1666', '-0.3198', '-0.2512', '0.2014', '0.4214', '-0.0808', '0.1014', '0.8486', '-0.04242', '-0.182', '-0.2433', '-0.3582', '0.257', '0.8022', '-0.3875', '0.1615', '0.0955', '0.001528', '-0.5005', '-0.1299', '-0.744', '-0.286', '-0.3308', '-0.353', '0.537', '0.3948', '0.2067', '-0.01327', '0.222', '-0.09094', '-1.135', '-0.1244', '0.668', '0.55', '-0.262', '-0.61', '-0.1473', '0.05148']",C3167,0000220,,204.9,,,0006721
mondo:0004969,acute quadriplegic myopathy,,,,,,,,0000225,,,,,
mondo:0004970,adenocarcinoma,"['adenocarcinoma NOS (morphologic abnormality)', 'adenocarcinoma, no subtype (morphologic abnormality)', 'adenocarcinomas', 'adenocarcinoma', 'ADNOS', 'adenocarcinoma, malignant']",299,,,C0001418,,C2852,0000228,D000230,,,,
mondo:0004971,adenoid cystic carcinoma,"['cylindroid adenocarcinoma', 'cylindroma', 'adenocystic carcinoma', 'cribriform carcinoma', 'adenoid cystic carcinoma', 'adenoid cystic cancer']",0080202,,,C0010606,,C2970,0000231,D003528,,,,
mondo:0004972,adenoma,"['adenomas', 'acinar cell adenoma', 'acinic cell adenoma', 'acinar cell adenoma (morphologic abnormality)', 'adenoma', 'adenoma, benign']",657,,,C0001430,,C2855,0000232,D000236,,,,
mondo:0004973,adenosquamous lung carcinoma,"['adenosquamous lung carcinoma', 'adenosquamous cell lung carcinoma', 'lung adenosquamous carcinoma', 'adenosquamous lung cancer']",4829,,,C0279557,,C9133,0000233,,162.9,,,
mondo:0004974,adrenal gland pheochromocytoma,"['pheochromocytoma (adrenal)', 'PCC', 'adrenal gland paraganglioma', 'adrenal gland pheochromocytoma', 'adrenal medullary pheochromocytoma', 'adrenal pheochromocytoma', 'adrenal gland Chromaffinoma', 'chromaffin paraganglioma of the adrenal gland', 'adrenal gland chromaffin paraganglioma', 'pheochromocytoma', 'adrenal medullary paraganglioma', 'Intraadrenal paraganglioma']",0050892,,,,"['-0.3127', '0.7896', '0.147', '-0.2246', '-0.5923', '0.4785', '0.506', '0.4155', '-0.2524', '-0.4258', '0.364', '-0.05975', '0.018', '0.1692', '-0.663', '-0.0564', '-0.757', '0.01079', '-0.05728', '-0.09235', '0.2449', '-0.6147', '0.328', '-0.08105', '0.06433', '-0.01666', '-0.10144', '-0.4404', '0.0855', '-0.35', '0.6377', '0.03183', '0.6626', '-0.1744', '-0.4648', '-0.0949', '-0.778', '0.4822', '0.1929', '-0.3774', '-0.1344', '0.03522', '0.3276', '-0.2161', '0.88', '-0.4543', '-0.1478', '0.1614', '0.3887', '-0.1251', '-0.02588', '0.58', '0.01537', '-0.05887', '-0.0986', '0.262', '0.0826', '0.5024', '-0.1167', '-0.3564', '-0.2556', '0.043', '0.0722', '-0.4023', '-0.4312', '1.058', '0.3225', '0.3633', '-0.03677', '0.713', '0.4792', '0.2817', '0.2318', '-0.5347', '-0.3882', '0.746', '-0.1267', '0.799', '-0.0927', '-0.7515', '-0.1273', '-0.23', '-0.09204', '-0.0927', '-0.09515', '-0.1521', '0.672', '0.04187', '0.3567', '0.0786', '-0.4639', '-0.456', '0.4104', '-0.0921', '0.963', '0.3357', '-0.11646', '-0.08545', '-0.147', '0.9937']",C3326,0000239,,,,,
mondo:0004975,Alzheimer disease,"['Alzheimers disease', 'Alzheimer disease, familial', 'Alzheimer dementia', 'presenile and senile dementia', 'Alzheimer^s dementia', 'Alzheimer disease', 'Alzheimer^s disease', 'AD', 'Alzheimers dementia']",10652,,238616,C0002395,"['-0.0458', '0.323', '0.2903', '0.1038', '-0.2072', '-0.2003', '0.022', '0.3804', '-0.3547', '-0.0746', '-0.01695', '-0.06445', '-0.2986', '-0.09155', '0.4238', '-0.5073', '-0.1025', '-0.0941', '-0.1703', '-0.4917', '0.1289', '-0.4187', '-0.05902', '0.0627', '0.4016', '-0.343', '-0.1146', '-0.1255', '-0.6675', '0.3013', '0.1558', '0.08545', '0.15', '-0.06113', '0.3901', '0.04395', '0.012886', '0.006466', '-0.06198', '-0.3586', '0.1923', '-0.426', '0.09784', '0.10834', '0.3325', '-0.3494', '-0.09753', '-0.1459', '0.01559', '0.2808', '0.1798', '0.509', '-0.3645', '-0.08594', '0.233', '-0.1084', '0.275', '-0.1371', '-0.3472', '0.01261', '-0.2091', '0.0605', '0.04642', '-0.157', '-0.0998', '0.00761', '0.31', '0.4568', '-0.1658', '0.2081', '0.1088', '0.09607', '0.1655', '-0.1982', '-0.1396', '0.2399', '0.2563', '0.437', '-0.6797', '-0.3667', '0.2179', '-0.5825', '-0.3015', '0.2822', '0.1846', '-0.1235', '0.06116', '0.1162', '0.348', '0.2913', '0.4136', '0.292', '0.10205', '0.3818', '0.0784', '0.08905', '0.3152', '0.05017', '0.1161', '0.1726']",C2866,0000249,D000544,331.0,G30,,0002511
mondo:0004976,amyotrophic lateral sclerosis,"['Lou Gehrig^s disease', 'Lou Gehrig disease', 'motor neuron disease, bulbar', 'ALS', 'Charcot disease']",332,,803,C0002736,"['0.358', '0.782', '-0.3337', '0.035', '-0.04044', '-0.291', '0.867', '0.818', '-0.7026', '-0.5195', '0.00817', '-0.337', '-0.4622', '0.2927', '0.742', '-0.4658', '-0.5195', '-0.3904', '-0.3406', '-0.4302', '-0.2544', '-0.2437', '0.08563', '0.091', '0.02347', '-0.1048', '0.2374', '0.2433', '-0.6826', '0.3328', '0.3403', '-0.1882', '-0.002705', '-0.4587', '0.3713', '-0.02237', '-0.286', '0.01686', '0.1843', '-0.2258', '0.1509', '0.1581', '-0.356', '-0.1707', '0.03314', '0.5376', '-0.2251', '-0.3115', '-0.15', '0.4805', '-0.4558', '-0.0761', '0.05533', '-0.3113', '0.221', '-0.1409', '-0.04324', '-0.3079', '-0.3381', '-0.4204', '0.242', '0.3442', '0.11816', '0.3176', '-0.3687', '0.1821', '-0.0373', '0.7324', '-0.3132', '0.5684', '-0.02907', '-0.1857', '0.3643', '-0.288', '0.6987', '0.3098', '-0.1584', '0.6064', '-0.2974', '-0.362', '0.006737', '-0.2998', '0.3567', '0.1437', '0.06183', '0.1737', '-0.3733', '0.07416', '0.6797', '-0.5786', '-0.3877', '-0.4949', '-0.421', '0.2732', '-0.1354', '0.2194', '0.4722', '-0.0721', '0.05588', '-0.0257']",C34373,0000253,D000690,335.20,G12.21,10002026,
mondo:0004977,angioimmunoblastic T-cell lymphoma,"['AITL', 'angioimmunoblastic T-cell lymphoma', 'AILT', 'angioimmunoblastic lymphadenopathy type T-cell lymphoma', 'AILD', 'angioimmunoblastic lymphadenopathy', 'T-cell lymphoma, AILD type', 'angioimmunoblastic lymphadenopathy with Dysproteinemia', 'immunoblastic lymphadenopathy', 'lymphogranulomatosis X']",0111147,,86886,C0020981,,C7528,0000255,D007119,202.70,C86.5,10002449,
mondo:0004979,asthma,"['chronic obstructive asthma', 'exercise induced asthma', 'exercise-induced asthma', 'bronchial hyperreactivity', 'chronic obstructive asthma with acute exacerbation', 'chronic obstructive asthma with status asthmaticus']",2841,,,C0004096,"['-0.002586', '0.411', '-0.04428', '0.1553', '-0.12244', '-0.42', '0.427', '0.1487', '-0.5034', '-0.4072', '0.5493', '0.3567', '-0.2576', '0.435', '-0.1737', '0.1098', '-0.294', '0.1455', '-0.606', '-0.8184', '0.08765', '0.03238', '0.04654', '-0.316', '-0.5806', '-1.019', '0.2117', '0.1803', '0.337', '-0.6665', '0.4033', '-0.306', '0.2617', '0.0935', '-0.6523', '-0.0437', '-0.8623', '0.2986', '0.822', '-0.272', '0.2551', '-0.01475', '0.2455', '-0.198', '-0.0664', '-0.2676', '-0.1384', '-0.09924', '0.4792', '0.7163', '-0.695', '0.04288', '0.352', '0.0416', '0.345', '0.2042', '-0.787', '0.5596', '0.193', '-0.42', '-0.2386', '1.052', '-0.1306', '0.10944', '0.3442', '0.1504', '0.9795', '0.4004', '-0.2834', '1.131', '-0.03174', '-0.2324', '0.2637', '-0.04398', '0.3853', '0.6753', '0.1554', '0.538', '-0.07086', '-0.2717', '0.006107', '-0.393', '-0.5146', '0.05203', '0.4915', '0.2188', '0.1857', '0.5615', '0.5947', '0.08594', '0.34', '-0.06415', '-0.78', '0.67', '0.1951', '0.529', '-0.7607', '-0.2595', '-0.3584', '-0.2766']",C28397,0000270,D001249,493.9,J45,,0002099
mondo:0004980,atopic eczema,"['eczema', 'atopic eczema', 'allergic', 'Besnier^s prurigo', 'eczematous dermatitis', 'Atopic dermatitis', 'allergic dermatitis', 'Atopic neurodermatitis', 'allergic form of dermatitis']",3310,,,,"['0.304', '0.2878', '-0.5117', '0.2512', '-0.4036', '-0.1339', '-0.1322', '0.134', '-0.6294', '0.06396', '0.3118', '0.4727', '-0.5684', '0.1819', '-0.546', '-0.1477', '0.03052', '0.0825', '-0.266', '-0.737', '-0.625', '0.4421', '0.257', '-0.291', '-0.3706', '-0.3079', '-0.5376', '0.39', '-0.4526', '-0.4214', '-0.1268', '-0.1351', '-0.2108', '0.633', '0.1571', '0.08997', '-0.7373', '0.0099', '-0.2332', '-0.12134', '0.254', '-0.409', '-0.2319', '0.2102', '-0.2389', '-0.261', '0.0862', '0.2507', '0.746', '0.5093', '-0.525', '-0.5723', '0.236', '0.226', '-0.1272', '0.2915', '0.010635', '0.3887', '-0.4797', '-1.028', '0.03078', '0.9023', '-0.04715', '0.1613', '0.869', '0.4436', '0.503', '0.3516', '-0.3193', '0.7944', '0.1686', '-0.0757', '0.2357', '-0.221', '-0.0892', '0.4385', '-0.00641', '0.4006', '0.3298', '0.10657', '0.1506', '-0.4104', '-0.4287', '0.1235', '0.3325', '0.224', '-0.2328', '0.01535', '0.4343', '0.7466', '-0.1423', '-0.1225', '-0.4673', '0.263', '0.462', '0.0572', '-0.3953', '-0.8364', '0.05322', '-0.4688']",C3001,0000274,,691.8,,,
mondo:0004981,atrial fibrillation,"['A-fib', 'AFib', 'atrial fibrillation', 'AF', 'atrial fibrillation (disease)']",0060224,,,C0004238,"['0.2355', '0.5874', '-0.4885', '-0.0385', '0.3086', '-0.2089', '0.5757', '0.453', '0.3801', '-0.64', '0.548', '-0.2632', '0.3315', '0.7603', '-0.4287', '-0.2793', '-0.7183', '-0.0872', '-0.671', '-0.5815', '0.5864', '0.692', '0.329', '0.014885', '0.2189', '-0.804', '0.1378', '0.04266', '0.7026', '-0.1611', '0.733', '0.7275', '0.5767', '0.521', '-0.219', '-0.225', '-0.386', '0.5083', '0.919', '-0.5146', '0.2136', '0.2284', '0.1598', '0.158', '0.645', '0.0358', '-0.1075', '-0.344', '0.507', '0.5024', '-0.1059', '0.492', '-0.5283', '-0.507', '0.071', '-0.3174', '-0.553', '0.2964', '-0.994', '-0.3125', '-0.09015', '1.018', '0.04675', '-0.3074', '-0.1794', '0.1372', '0.822', '0.9766', '-0.6426', '0.2622', '0.09076', '0.9224', '0.169', '-0.321', '0.0942', '0.452', '0.4124', '0.07855', '-0.6265', '-0.2184', '-0.2712', '-0.1638', '0.04987', '0.1576', '0.7153', '0.03024', '0.682', '-0.014404', '0.2808', '0.1288', '0.0945', '-0.2397', '-0.2876', '0.4011', '0.6113', '0.4138', '0.1473', '-0.3752', '-1.084', '-0.3052']",C50466,0000275,D001281,427.31,,,0005110
mondo:0004982,pancreatitis,['pancreas inflammation'],4989,,,C0030305,,C3306,0000278,D010195,,,,
mondo:0004983,spermatogenic failure,['spermatogenic failure'],0111910,,,,,,,,,,,
mondo:0004984,basal-like breast carcinoma,"['basal-like breast carcinoma', 'basal-like breast cancer', 'basal-like subtype of breast carcinoma']",,,,C3642347,,C53558,0000281,,,,,
mondo:0004985,bipolar disorder,"['manic bipolar I disorder', 'major affective disorder', 'bipolar disorder manic phase', 'manic bipolar affective disorder', 'bipolar depression', 'manic disorder', 'depressive-manic psych.', 'mixed bipolar disorder', 'manic-depression', 'bipolar disorder', 'manic depressive disorder', 'manic depression', 'MAFD']",3312,,,C0005586,"['0.2228', '0.05536', '-0.4539', '0.6167', '-0.4385', '-0.09094', '0.1364', '0.831', '-0.1481', '0.2112', '0.46', '-0.1465', '0.655', '0.4426', '0.1555', '-0.1578', '-0.9697', '0.126', '-0.542', '-0.7065', '-0.5063', '0.344', '0.8945', '-0.3857', '0.636', '-0.23', '0.08636', '-0.2866', '0.578', '-0.2235', '0.3762', '-0.2456', '0.5747', '0.1735', '-0.4424', '-0.2367', '-0.9805', '0.2222', '0.3594', '-0.3074', '0.9814', '-0.1827', '-0.529', '-0.0791', '0.849', '-0.3403', '-0.1531', '0.1243', '-0.002422', '0.774', '-0.1211', '0.2183', '-0.539', '-0.03604', '0.845', '0.661', '0.1473', '0.1294', '-0.3967', '-0.3367', '-0.903', '0.0741', '-0.2208', '0.254', '-0.2937', '0.6533', '0.08374', '0.2644', '-0.401', '0.5747', '-0.1853', '0.1719', '0.11456', '-0.984', '-0.06903', '0.5244', '-0.3225', '0.763', '-0.04977', '0.2854', '0.3772', '-0.1754', '-0.4111', '0.291', '0.1279', '0.237', '0.004677', '0.0691', '0.3938', '0.5547', '-0.2439', '0.434', '-0.735', '0.6064', '0.00417', '0.1803', '-0.0313', '-0.575', '0.0758', '0.7505']",C34423,0000289,D001714,296.89,F31,,
mondo:0004986,urinary bladder carcinoma,"['bladder cancer', 'bladder carcinoma', 'carcinoma of urinary bladder', 'carcinoma of the bladder', 'carcinoma of bladder', 'cancer of the bladder', 'cancer of the urinary bladder', 'urinary bladder carcinoma', 'carcinoma bladder', 'cancer of urinary bladder', 'urinary bladder cancer', 'cancer of bladder', 'carcinoma of the urinary bladder']",4007,,,C0699885,"['-0.0843', '0.1075', '0.01195', '0.07654', '-0.01872', '-0.1263', '0.1265', '0.1216', '-0.12476', '-0.033', '-0.0689', '-0.1298', '-0.1858', '0.1346', '-0.2168', '-0.1148', '-0.0509', '-0.1053', '0.10596', '-0.2698', '-0.02316', '-0.09344', '0.0952', '-0.1748', '0.1825', '-0.07416', '-0.02925', '0.02994', '-0.135', '-0.0802', '0.2146', '-0.009895', '0.06097', '-0.0477', '0.01625', '-0.0171', '-0.0321', '0.10156', '-0.001166', '-0.1404', '-0.05328', '-0.1975', '0.09186', '-0.1288', '-0.02748', '-0.1713', '-0.03836', '-0.04846', '0.0783', '0.07874', '-0.02745', '0.09515', '0.02437', '-0.0364', '-0.1821', '-0.00711', '0.217', '-0.05447', '-0.2673', '-0.0762', '0.2095', '0.1103', '-0.0378', '0.04813', '0.07184', '0.1359', '0.32', '0.1987', '-0.1515', '0.2517', '-0.01616', '0.0734', '0.07886', '-0.03452', '0.02951', '0.02393', '-0.0633', '0.07947', '-0.1064', '-0.2798', '-0.1992', '0.02063', '0.0534', '0.0379', '-0.1178', '-0.02563', '0.0591', '-0.000879', '0.2129', '-0.197', '0.004158', '0.2338', '0.00503', '-0.01193', '0.3254', '0.03111', '0.1409', '-0.2522', '-0.079', '0.205']",C4912,0000292,,,,,0002862
mondo:0004987,urinary bladder neoplasm,"['bladder tumours', 'tumor of urinary bladder', 'tumour of the bladder', 'bladder tumour', 'neoplasm of the urinary bladder', 'urinary bladder neoplasm (disease)', 'urinary bladder tumours', 'urinary bladder neoplasms', 'tumour of the urinary bladder', 'urinary bladder tumor', 'tumour of bladder', 'bladder tumors', 'urinary bladder neoplasm', 'tumor of the bladder', 'tumor of the urinary bladder', 'tumor of bladder', 'neoplasm of urinary bladder', 'urinary bladder tumors', 'bladder tumor', 'bladder neoplasm', 'neoplasm of the bladder', 'tumour of urinary bladder', 'urinary bladder tumour', 'neoplasm of bladder']",,,,C0005695,,C2901,0000294,,239.4,,,
mondo:0004988,breast adenocarcinoma,"['mammary adenocarcinoma', 'adenocarcinoma of the breast', 'breast adenocarcinoma', 'adenocarcinoma of breast']",3458,,,,,C5214,0000304,,,,,
mondo:0004989,breast carcinoma,"['breast cancer, NOS', 'carcinoma of the breast', 'cancer, breast', 'breast cancer', 'carcinoma of breast', 'mammary carcinoma', 'cancer of the breast', 'breast carcinoma', 'cancer of breast']",3459,,,C0678222,"['-0.0551', '0.1296', '-0.03006', '0.0804', '0.0699', '-0.1743', '0.06354', '0.06256', '-0.07477', '-0.0935', '0.003592', '0.007397', '-0.0997', '0.1383', '-0.197', '-0.2173', '0.0193', '-0.1393', '0.05847', '-0.259', '-0.08093', '-0.158', '0.1671', '-0.2311', '0.2112', '-0.11835', '-0.00631', '0.0408', '-0.05997', '-0.2261', '0.2452', '0.0425', '0.1382', '-0.103', '0.01714', '-0.0244', '-0.09406', '0.0839', '0.04532', '-0.1079', '0.005085', '-0.179', '0.011635', '-0.0907', '0.01778', '-0.0717', '-0.01354', '-0.0363', '0.1228', '0.02153', '0.04916', '-0.006145', '0.002443', '0.136', '-0.2023', '-0.03754', '0.1777', '-0.03815', '-0.2913', '0.003807', '0.231', '0.0735', '0.002094', '0.0538', '0.03735', '0.1511', '0.3154', '0.2166', '-0.1975', '0.1942', '0.01391', '0.03464', '0.1169', '-0.055', '0.0626', '-0.00516', '-0.02089', '-0.02222', '-0.1074', '-0.2225', '-0.2407', '0.03464', '0.0311', '0.02365', '-0.1815', '-0.1226', '0.0485', '0.0631', '0.2069', '-0.07324', '0.0313', '0.3164', '-0.00235', '-0.01909', '0.3616', '0.04486', '0.09924', '-0.1906', '-0.0822', '0.1052']",C4872,0000305,,,,,
mondo:0004990,breast tumor luminal A or B,"['luminal breast cancer', 'luminal breast carcinoma', 'breast tumour luminal', 'breast tumor luminal']",0060548,,,,,,0000306,,,,,
mondo:0004991,minimally invasive lung adenocarcinoma,"['bronchioloalveolar adenocarcinoma of the lung', 'bronchioloalveolar lung adenocarcinoma', 'bronchiolo-alveolar carcinoma of lung', 'bronchioloalveolar adenocarcinoma of lung', 'bronchiolo-alveolar carcinoma of the lung', 'bronchiolo-alveolar lung carcinoma', 'bronchioloalveolar carcinoma', 'bronchiolo-alveolar adenocarcinoma', 'bac', 'bronchioalveolar adenocarcinoma of the lung', 'carcinoma, bronchioloalveolar, malignant', 'bronchioalveolar lung carcinoma', 'minimally invasive lung adenocarcinoma', 'bronchioalveolar adenocarcinoma of lung']",4926,,,,,C2923,0000308,D002282,162.9,,,
mondo:0004992,cancer,"['primary cancer', 'malignant neoplasm', 'malignant neoplastic disease', 'neoplasm, malignant', 'MT', 'malignant tumor', 'cancer', 'cell type cancer', 'malignant Growth', 'organ system cancer', 'malignant tumour', 'CA', 'malignancy', 'neoplasm (disease), malignant']",162,,,C0006826,,C9305,0000311,,199.1,,,
mondo:0004993,carcinoma,"['malignant epithelial tumor', 'epithelioma', 'malignant epithelioma', 'malignant epithelial tumour', 'Other carcinoma', 'epithelioma malignant', 'epithelial carcinoma', 'carcinoma', 'carcinoma, malignant', 'malignant epithelial neoplasm']",305,,,C0007097,,C2916,0000313,D002277,,,,
mondo:0004994,cardiomyopathy,"['cardiomyopathy', 'Cardiomyopathies']",0050700,,167848,C0878544,,C34830,0000318,D009202,425.9,I42,10007636,
mondo:0004995,cardiovascular disorder,"['disease of cardiovascular system', 'cardiovascular system disease or disorder', 'cardiovascular disorder', 'cardiovascular disease (CVD)', 'circulatory system disease', 'disease of subdivision of hemolymphoid system', 'cardiovascular system disease', 'cardiovascular disease', 'disorder of cardiovascular system']",1287,,,C0007222,,C2931,0000319,D002318,459.9,,,
mondo:0004996,childhood acute myeloid leukemia,"['childhood acute myelogenous leukemia', 'paediatric AML', 'childhood acute myelogenous leukaemia', 'acute myeloid leukemia (AML)', 'pediatric acute myelocytic leukemia', 'pediatric acute myeloid leukemia', 'paediatric acute myeloid leukaemia', 'pediatric AML', 'paediatric acute myelocytic leukaemia', 'pediatric acute myelogenous leukemia', 'childhood acute granulocytic leukemia', 'acute myeloid leukaemia (AML)', 'childhood acute granulocytic leukaemia', 'paediatric acute myelogenous leukaemia', 'childhood AML', 'acute myeloid leukemia of childhood', 'pediatric acute myeloblastic leukemia', 'acute myeloid leukaemia of childhood', 'childhood acute myeloblastic leukaemia', 'childhood acute myelocytic leukaemia', 'paediatric acute myeloblastic leukaemia', 'childhood acute myelocytic leukemia', 'childhood acute myeloblastic leukemia', 'childhood acute myeloid leukemia']",0070323,,,C0220621,,C9160,0000330,,,,,
mondo:0004997,chondroblastoma,"['chondroblastoma', 'chondroblastoma (disease)', 'chondroblastoma of bone', 'CHBL']",2649,,,C0008441,,C2945,0000331,D002804,,,,0030432
mondo:0005001,chronic gastritis,"['chronic gastritis', 'chronic gastritis (disease)', 'gastritis (disease), chronic']",,,,C0085695,,C26929,0000337,,535.41,,,0005231
mondo:0005002,chronic obstructive pulmonary disease,"['COPD, chronic obstructive pulmonary disease', 'chronic obstructive lung disease', 'chronic obstructive airways disease', 'obstructive lung disease, chronic', 'COPD', 'obstructive pulmonary disease (COPD), chronic', 'cold', 'disease (COPD), chronic obstructive', 'cold (chronic obstructive lung disease)', 'chronic obstructive airway disease', 'chronic obstructive pulmonary disease, (COPD)', 'pulmonary disease (COPD), chronic obstructive', 'chronic obstructive pulmonary disease (COPD)']",3083,606963,,,,C3199,0000341,D029424,496,,,
mondo:0005003,chronic pancreatitis,"['pancreatitis, chronic']",,,,C0149521,"['0.03754', '0.3308', '-0.02473', '0.07587', '-0.5874', '0.05487', '0.415', '0.157', '-0.5273', '0.0975', '0.1663', '-0.3523', '0.08795', '0.548', '-0.789', '-0.3987', '0.1328', '0.825', '-0.364', '-0.4978', '-0.164', '-0.01843', '0.463', '-0.466', '0.10187', '0.09515', '0.3884', '0.72', '0.2595', '-0.555', '-0.347', '-0.159', '0.6157', '-0.1749', '0.0853', '0.2598', '-0.808', '0.0649', '0.4707', '-0.03363', '-0.6816', '0.149', '-0.01703', '0.347', '-0.5864', '-0.2769', '0.3645', '-0.487', '0.2095', '0.1533', '0.0811', '-0.02182', '0.4585', '-0.1714', '0.2695', '0.4463', '-0.1595', '-0.05795', '-0.637', '-0.2051', '0.4097', '0.4336', '0.0904', '-0.985', '-0.3423', '0.5166', '0.4426', '0.5454', '-0.3052', '0.1537', '0.03278', '0.3865', '0.4', '-0.2742', '0.4883', '0.2725', '0.3955', '0.848', '-0.1409', '-0.1992', '-0.9175', '0.09344', '-0.3196', '-0.2327', '0.1699', '0.1636', '0.3936', '0.6646', '1.03', '-0.2286', '0.2124', '-0.2499', '-0.4443', '0.6797', '0.9463', '-0.02628', '-0.3652', '-0.849', '-0.611', '0.7314']",C84637,0000342,D050500,577.1,,,
mondo:0005004,clear cell adenocarcinoma,"['malignant mesonephroma', 'clear cell adenocarcinoma (morphologic abnormality)', 'mesonephroma, malignant (morphologic abnormality)', 'water-clear cell adenocarcinoma', 'adenocarcinoma, clear cell, malignant', 'Wolffian duct neoplasm', 'clear cell carcinoma', 'water-clear cell adenocarcinoma (morphologic abnormality)', 'clear cell adenocarcinoma NOS (morphologic abnormality)', 'mesonephroid clear cell carcinoma', 'clear cell adenocarcinoma', 'mesonephroma, malignant', 'mesonephroma NOS (morphologic abnormality)', 'water-clear cell carcinoma', 'mesonephroid clear cell adenocarcinoma']",4468,,,C0206681,,C4072,0000348,D018262,,,,
mondo:0005005,clear cell renal carcinoma,"['clear cell adenocarcinoma, kidney', 'kidney clear cell adenocarcinoma', 'RCC, clear cell adenocarcinoma', 'conventional (clear cell) renal cell adenocarcinoma', 'Grawitz tumour', 'conventional (clear cell) renal cell carcinoma', 'clear cell renal cell cancer', 'renal clear cell carcinoma', 'Grawitz tumor', 'clear cell carcinoma of the kidney', 'clear cell kidney carcinoma', 'renal clear cell adenocarcinoma', 'kidney clear cell carcinoma', 'clear cell renal cell carcinoma', 'conventional renal cell carcinoma', 'renal cell carcinoma, clear cell adenocarcinoma', 'clear-cell metastatic renal cell carcinoma', 'clear cell carcinoma of kidney', 'clear cell adenocarcinoma of the kidney', 'clear cell adenocarcinoma of kidney', 'hypernephroma']",4467,,319276,,"['-0.1126', '0.08844', '0.014565', '0.09686', '0.03162', '-0.0952', '0.1469', '0.0807', '-0.02304', '-0.02463', '0.03723', '-0.03348', '-0.071', '0.1705', '-0.2715', '-0.2085', '-0.0718', '-0.2352', '0.1533', '-0.334', '0.0327', '-0.244', '0.2079', '-0.1636', '0.0835', '-0.0888', '-0.01913', '-0.04205', '-0.1718', '0.03427', '0.3435', '-0.02809', '0.2472', '-0.04498', '0.1206', '-0.00723', '-0.1816', '0.08636', '-0.07904', '-0.0994', '0.1254', '-0.2673', '0.2031', '-0.152', '0.06134', '-0.01901', '-0.079', '-0.03116', '0.1893', '0.03787', '0.1405', '-0.04196', '0.12415', '0.0996', '-0.2347', '0.01092', '0.087', '-0.073', '-0.3596', '-0.09564', '0.4392', '0.03076', '-0.2277', '0.1538', '0.0869', '-0.0689', '0.3354', '0.3064', '-0.0839', '0.441', '0.09705', '-0.10516', '0.0489', '0.07477', '0.0001341', '0.06604', '-0.16', '0.2494', '-0.0838', '-0.3645', '-0.252', '0.0828', '-0.2161', '0.0768', '-0.3362', '-0.2328', '0.2051', '0.05197', '0.2053', '-0.1486', '0.1732', '0.1815', '-0.1586', '-0.0411', '0.4211', '-0.02359', '0.2067', '-0.316', '-0.1968', '0.1221']",C4033,0000349,,189.0,,,
mondo:0005006,clear cell sarcoma of kidney,"['clear cell sarcoma - kidney', 'paediatric renal clear cell sarcoma', 'pediatric renal clear cell sarcoma', 'pediatric kidney clear cell sarcoma', 'clear cell sarcoma of kidney', 'renal clear cell sarcoma', 'childhood kidney clear cell sarcoma', 'paediatric kidney clear cell sarcoma', 'childhood renal clear cell sarcoma', 'kidney clear cell sarcoma', 'CCSK', 'clear cell sarcoma of the kidney', 'childhood clear cell sarcoma of the kidney']",4880,,457246,CN242113,,C4264,0000350,,,,,
mondo:0005007,colon mucinous adenocarcinoma,"['colonic colloid adenocarcinoma', 'mucinous adenocarcinoma of colon', 'mucinous colon adenocarcinoma', 'colloid adenocarcinoma of the colon', 'colloidal colon adenocarcinoma', 'colloid colon adenocarcinoma', 'colloidal adenocarcinoma of colon', 'colon colloidal adenocarcinoma', 'colon colloid adenocarcinoma', 'mucinous adenocarcinoma of the colon', 'colonic mucinous adenocarcinoma', 'colloid adenocarcinoma of colon', 'colonic colloidal adenocarcinoma', 'colloidal adenocarcinoma of the colon', 'colon mucinous adenocarcinoma']",3029,,,C0279639,,C7966,0000364,,,,,
mondo:0005008,colorectal adenocarcinoma,"['adenocarcinoma of large intestine', 'large bowel adenocarcinoma', 'colorectal (colon or rectal) adenocarcinoma', 'adenocarcinoma of large bowel', 'adenocarcinoma of the large bowel', 'colorectal adenocarcinoma', 'colorectum adenocarcinoma', 'large intestine adenocarcinoma', 'adenocarcinoma of the large intestine']",0050913,,,C1319315,"['-0.1254', '0.1338', '0.0729', '-0.02823', '0.03983', '-0.2053', '0.161', '0.03735', '-0.00783', '0.02179', '-0.12146', '-0.05853', '-0.1744', '0.02649', '-0.4038', '-0.2275', '-0.03195', '-0.2', '0.2815', '-0.1855', '-0.2013', '-0.2544', '0.3875', '-0.3164', '0.4092', '-0.12463', '-0.01225', '0.002516', '-0.1547', '-0.195', '0.356', '-0.008736', '0.08527', '-0.12146', '0.2279', '-0.076', '-0.332', '0.012596', '0.02588', '-0.2598', '0.02711', '-0.3542', '0.238', '-0.1654', '0.10864', '-0.10565', '-0.108', '-0.02629', '0.2316', '-0.1567', '0.1395', '-0.1415', '-0.1187', '0.10583', '-0.4028', '-0.1133', '0.2225', '-0.01237', '-0.4988', '0.02567', '0.3364', '0.09644', '-0.2006', '0.0858', '0.1392', '0.00901', '0.4856', '0.2275', '-0.01559', '0.4844', '0.05188', '0.0197', '0.1478', '-0.01927', '-0.01659', '0.03226', '-0.2129', '-0.02692', '-0.02759', '-0.3245', '-0.3442', '0.1421', '-0.1588', '-0.0375', '-0.4053', '-0.2856', '0.1315', '0.1186', '0.1555', '-0.2983', '0.0709', '0.3394', '0.0399', '-0.07825', '0.4321', '-0.02307', '0.346', '-0.443', '-0.3625', '0.011246']",C5105,0000365,,,,,
mondo:0005009,congestive heart failure,"['heart failure, congestive', 'failure, congestive heart', 'CHF', 'weak heart', 'congestive heart disease', 'cardiac failure, congestive']",6000,,,C0018802,,C3080,0000373,,428.9,,,
mondo:0005010,coronary artery disorder,"['coronary arteriosclerosis', 'coronary disease', 'coronary artery disease', 'CAD', 'disorder of coronary artery', 'disease of coronary artery', 'coronary heart disease', 'coronary artery disease or disorder', 'CHD (coronary heart disease)', 'CHD']",3393,,,C1956346,"['-0.0188', '0.02272', '-0.279', '0.2086', '0.224', '-0.4963', '-0.006348', '0.3066', '0.01385', '-0.5923', '0.1847', '-0.2001', '0.6304', '0.2102', '-0.5103', '-0.2808', '-0.3245', '0.595', '-0.1549', '-0.1709', '0.7188', '-0.1548', '0.4167', '0.2451', '-0.2654', '-0.2825', '0.1076', '0.2715', '0.3926', '0.2993', '0.5894', '-0.254', '0.628', '-0.0654', '-0.1919', '-0.10535', '0.03403', '-0.006287', '0.5747', '-0.603', '0.3218', '0.1186', '0.3865', '0.153', '0.7275', '0.1902', '0.1377', '0.2029', '-0.0161', '0.448', '0.2617', '0.03644', '0.4548', '-0.1368', '-0.165', '-0.2974', '-0.4553', '0.4587', '-0.1929', '-0.2822', '-0.4456', '0.81', '-0.02802', '-0.5', '-0.289', '0.6914', '0.603', '0.5024', '-0.552', '0.2705', '-0.0915', '0.1116', '0.3584', '-0.5273', '0.265', '0.7915', '0.2294', '0.2051', '-0.6787', '0.1852', '-0.4148', '-0.4553', '-0.1472', '-0.1633', '0.257', '0.2634', '0.02669', '0.4084', '0.5903', '-0.04633', '-0.0988', '-0.0633', '-0.2893', '0.7773', '0.5767', '-0.0659', '-0.3254', '-0.2507', '-0.889', '-0.1741']",C26732,0001645,D017202,414.9,,,
mondo:0005011,Crohn disease,"['Crohn^s disease of colon', 'Crohn^s disease', 'Crohn^s disease of large bowel', 'pediatric Crohn^s disease', 'Crohn disease', 'granulomatous colitis', 'paediatric Crohn^s disease', 'regional enteritis']",8778,,206,CN043071,"['0.1392', '0.2091', '-0.03708', '0.646', '-0.04517', '0.2566', '0.2235', '0.4797', '-0.228', '-0.0825', '0.287', '0.07733', '-0.831', '0.4692', '-0.509', '-0.313', '-0.4216', '0.369', '-0.538', '-0.421', '0.4478', '-0.4844', '0.1373', '-0.646', '-0.07526', '-0.0843', '0.1263', '0.1203', '0.685', '-0.1953', '0.4841', '-0.6577', '-0.02164', '0.07837', '0.5293', '0.2428', '-0.587', '-0.439', '0.3936', '0.11957', '-0.002775', '-0.2822', '0.286', '-0.04443', '0.2236', '-0.09644', '0.2405', '-0.4087', '0.1637', '0.7183', '-0.5454', '-0.4065', '0.0656', '-0.1584', '-0.2245', '0.005836', '-0.3333', '0.356', '-0.5547', '-0.333', '0.1882', '0.4985', '0.2773', '-0.2756', '-0.0789', '0.2001', '0.798', '0.04834', '0.0456', '0.774', '0.165', '0.1772', '0.06226', '-0.2754', '-0.1779', '0.4248', '0.1705', '0.68', '0.1836', '-0.5176', '-0.4363', '-0.3528', '-0.2274', '-0.2634', '-0.0748', '-0.3667', '0.3445', '0.229', '-0.0951', '-0.2338', '0.06714', '-0.1018', '0.3691', '0.2416', '0.926', '0.4075', '-0.512', '-0.2722', '-0.622', '0.2008']",C2965,0000384,D003424,555.1,,,
mondo:0005012,cutaneous melanoma,"['zone of skin melanoma (disease)', 'malignant melanoma of skin of upper limb', 'cutaneous melanoma (disease)', 'cutaneous (skin) melanoma', 'malignant melanoma (of skin), stage unspecified', 'cutaneous melanoma', 'malignant melanoma of skin stage unspecified', 'malignant melanoma of skin of lower limb', 'melanoma of the skin', 'malignant lower limb melanoma', 'malignant trunk melanoma', 'malignant melanoma of skin of trunk except scrotum', 'melanoma of skin', 'malignant ear melanoma', 'malignant scalp melanoma', 'skin melanoma', 'malignant cutaneous melanoma', 'malignant melanoma of skin', 'malignant upper limb melanoma', 'skin, melanoma', 'malignant melanoma of ear and/or external auricular canal', 'malignant lip melanoma', 'malignant neck melanoma']",8923,,,C0153536,"['0.3691', '-0.0508', '-1.027', '0.3003', '0.5913', '0.2258', '-0.2908', '0.3083', '-0.742', '0.1312', '0.919', '0.0856', '-0.8203', '0.742', '-0.6104', '-0.2094', '0.4282', '-0.5405', '-0.10767', '-0.1499', '-0.1632', '0.292', '-0.3013', '-0.364', '0.2527', '-0.551', '-0.676', '-0.2053', '0.1885', '0.1624', '0.9146', '-0.724', '-0.03326', '-0.12305', '0.3743', '0.707', '-0.4907', '-0.04623', '0.1515', '-0.3938', '0.4568', '-0.931', '0.11444', '-0.0841', '-0.09', '-0.64', '-0.01974', '-0.3032', '0.0316', '-0.544', '0.0833', '-0.2715', '-0.0686', '-0.318', '-0.86', '-0.3958', '-0.02853', '0.02068', '-1.015', '-0.4824', '-0.2162', '-0.0626', '-0.9355', '0.8174', '0.00497', '1.354', '0.5366', '0.4229', '0.3193', '1.05', '0.3743', '0.6455', '0.26', '0.0988', '0.3098', '0.3', '-0.871', '0.55', '-0.1943', '-0.1335', '0.05408', '-0.265', '0.1149', '-0.2783', '-0.1292', '-0.966', '-0.0801', '0.2485', '1.225', '0.08105', '0.8276', '0.06415', '-0.4146', '0.609', '0.642', '0.5483', '-0.4316', '-0.9224', '-0.9487', '0.5327']",C3510,0000389,,172.9,,,0012056
mondo:0005013,dedifferentiated chondrosarcoma,"['Dedifferentiated chondrosarcoma', 'DDCHS']",0081247,,,C0862878,,C6476,0000394,,,,,
mondo:0005015,diabetes mellitus,"['diabetes mellitus (disease)', 'DM', 'diabetes', 'diabetes mellitus']",9351,,,C0011849,"['0.7144', '-0.11597', '0.2344', '0.8584', '-0.46', '-0.764', '-0.3325', '1.127', '-0.1742', '-0.692', '-0.0368', '-0.2866', '0.2305', '0.2195', '-0.9766', '-0.3364', '0.3496', '0.1426', '-0.0674', '-0.8364', '-0.01917', '-0.2235', '0.01692', '0.08105', '-0.829', '-0.4392', '0.07666', '0.02786', '0.5337', '-0.2476', '0.6597', '-0.3206', '-0.07', '-0.2358', '-0.2167', '0.6455', '-0.7534', '0.5776', '0.0367', '-0.1371', '-0.10504', '0.5986', '0.2603', '0.5474', '-0.4822', '-0.2993', '0.3687', '-0.4314', '0.3591', '0.166', '0.10486', '-0.2822', '0.9976', '-0.642', '-0.0477', '0.4695', '0.1902', '-0.849', '-1.017', '0.655', '-0.506', '0.4146', '-0.1993', '0.03317', '-0.10736', '0.615', '-0.225', '0.6436', '-0.864', '-0.0586', '0.2324', '0.446', '0.3176', '-0.1891', '0.5923', '0.5327', '-0.5405', '1.024', '-0.4592', '-0.1537', '0.0986', '0.11633', '-0.146', '-0.5366', '0.3188', '0.1023', '-0.01859', '0.471', '0.865', '0.2593', '0.6055', '0.4785', '-0.1858', '-0.3093', '1.259', '0.2852', '-0.1355', '-0.0951', '-0.1841', '0.4692']",C2985,0000400,D003920,250,E08-E13,,0000819
mondo:0005016,diabetic kidney disease,"['type 1 diabetes nephropathy', 'diabetic nephropathy', 'type 2 diabetes nephropathy', 'DKD']",11503,,,,"['0.4395', '-0.01607', '0.2065', '0.3984', '-0.3677', '-0.4202', '0.11255', '1.022', '-0.4324', '-0.33', '-0.3484', '-0.03845', '0.3901', '0.8574', '-0.3198', '-0.5366', '-0.1635', '0.406', '0.884', '-0.12024', '0.0873', '-0.721', '0.04678', '0.1497', '-0.0933', '-0.1063', '-0.05783', '0.3745', '0.325', '0.0947', '0.862', '0.1901', '0.6895', '0.1752', '0.00826', '-0.2244', '-0.4326', '0.215', '0.249', '-0.379', '-0.4666', '0.10565', '0.647', '-0.4043', '-0.1081', '-0.174', '-0.06805', '0.1068', '0.369', '-0.0434', '-0.3906', '0.2211', '0.4873', '-0.8706', '-0.1837', '0.2491', '0.2249', '0.0958', '-1.124', '-0.3132', '-0.5586', '0.01767', '-0.1078', '-0.09033', '0.07495', '0.09314', '-0.1356', '0.6123', '-0.7056', '0.3965', '-0.1978', '0.1829', '0.1626', '-0.3333', '0.6987', '0.02095', '0.4917', '0.694', '0.00413', '0.2324', '-0.194', '-0.453', '0.1715', '0.2808', '0.263', '-0.02946', '0.423', '0.05905', '0.11304', '0.36', '0.4072', '0.3103', '-0.796', '0.384', '0.2832', '0.2072', '-0.3237', '-0.3481', '-0.3933', '0.4248']",C84417,0004997,D003928,583.81,,,
mondo:0005017,diffuse gastric adenocarcinoma,"['diffuse adenocarcinoma of stomach', 'diffuse adenocarcinoma of the stomach', 'diffuse gastric adenocarcinoma', 'adenocarcinoma of the linitis plastica type', 'gastric diffuse adenocarcinoma', 'adenocarcinoma of linitis plastica type', 'carcinoma, diffuse type (morphologic abnormality)', 'carcinoma, diffuse type', 'stomach diffuse type adenocarcinoma', 'diffuse stomach adenocarcinoma', 'diffuse type stomach adenocarcinoma']",6217,,,,,C9159,0000402,,,,,
mondo:0005019,diffuse scleroderma,"['diffuse systemic sclerosis', 'systemic sclerosis, diffuse']",1580,,,,,C116791,0000404,D045743,,,,
mondo:0005020,intestinal disorder,"['intestine disease', 'disorder of intestine', 'intestinal disorder', 'diseases, intestinal', 'disease of intestine', 'disease, intestinal', 'intestinal disease', 'intestine disease or disorder']",5295,,,,,C26801,,D007410,575,,,
mondo:0005021,dilated cardiomyopathy,"['congestive cardiomyopathy', 'idiopathic dilation cardiomyopathy', 'familial dilated cardiomyopathy', 'primary dilated cardiomyopathy']",12930,,217604,C0007193,"['0.3206', '-0.731', '-0.1543', '0.569', '0.01903', '-0.5654', '0.6143', '0.5796', '-0.2225', '-0.4863', '0.4407', '-0.4768', '-0.317', '0.3872', '-0.4075', '0.2327', '-0.784', '-0.0708', '-0.72', '-0.636', '0.3923', '0.4714', '0.4924', '-0.175', '0.4668', '-0.2024', '0.4714', '0.496', '-0.1495', '-0.4116', '0.8022', '-0.2311', '0.73', '0.3738', '-0.04636', '-0.602', '-0.3245', '-0.649', '0.73', '-0.502', '-0.08484', '0.771', '0.094', '0.622', '0.258', '0.2605', '0.2375', '0.6924', '0.82', '-0.684', '-0.2751', '0.1467', '0.665', '-0.0371', '0.587', '-0.5244', '-0.2805', '0.5356', '-0.761', '-0.1675', '-0.06107', '0.477', '0.4077', '-1.026', '-0.8843', '0.37', '0.1505', '0.3188', '-0.808', '0.01633', '-0.5044', '0.266', '0.1364', '-0.3245', '-0.224', '0.763', '-0.3088', '-0.03232', '-0.3071', '0.512', '0.05167', '-0.3062', '0.03035', '-0.4524', '1.176', '-0.109', '0.6255', '-0.07996', '0.6353', '0.3416', '0.0805', '0.07166', '-0.3135', '0.291', '1.035', '1.072', '0.318', '-0.5835', '-0.452', '-0.1487']",C84673,0000407,D002311,425.4,I42.0,10056370,0001644
mondo:0005023,ductal breast carcinoma in situ,"['non-invasive ductal carcinoma of the breast', 'non-invasive ductal breast carcinoma', 'non-infiltrating ductal carcinoma of breast', 'non-invasive ductal breast adenocarcinoma', 'stage 0 mammary duct carcinoma', 'non-invasive ductal carcinoma of breast', 'mammary duct in situ carcinoma', 'non-infiltrating ductal adenocarcinoma of the breast', 'breast ductal carcinoma in situ', 'non-invasive intraductal adenocarcinoma of the breast', 'non-infiltrating ductal breast carcinoma', 'ductal breast carcinoma in situ', 'non-invasive intraductal adenocarcinoma of breast', 'non-infiltrating intraductal carcinoma', 'intraductal carcinoma', 'intraductal breast carcinoma', 'ductal carcinoma in situ (DCIS)', 'non-infiltrating intraductal breast adenocarcinoma', 'carcinoma in situ of mammary duct', 'non-infiltrating intraductal adenocarcinoma', 'intraductal carcinoma of breast', 'non-invasive ductal adenocarcinoma of breast', 'DCIS', 'non-infiltrating ductal carcinoma of the breast', 'non-infiltrating ductal adenocarcinoma of breast', 'ductal carcinoma in situ of breast', 'non-infiltrating ductal breast adenocarcinoma', 'non-infiltrating intraductal adenocarcinoma of breast', 'non-infiltrating intraductal adenocarcinoma of the breast', 'intraductal carcinoma of the breast', 'non-invasive intraductal breast adenocarcinoma', 'non-invasive ductal adenocarcinoma of the breast', 'ductal carcinoma in situ', 'ductal carcinoma in situ of the breast']",0060074,,,,,C2924,0000432,D002285,233.0,,,
mondo:0005025,endocarditis,"['endocarditis (disease)', 'endocarditis', 'endocardium inflammation']",10314,,,,,C34582,0000465,D004696,424.99,,,0100584
mondo:0005026,endometrioid adenocarcinoma,"['endometrioid carcinoma of female reproductive system', 'endometrioid adenocarcinoma', 'endometrioid carcinoma of the female reproductive system', 'endometrioid carcinoma', 'female reproductive endometrioid carcinoma']",,,,C1569637,,C3769,0000466,,,,,
mondo:0005027,epilepsy,['seizure disorder'],1826,,,,,C3020,0000474,D004827,345.91,G40,,
mondo:0005028,esophageal adenocarcinoma,"['esophagus adenocarcinoma', 'esophageal adenocarcinoma', 'adenocarcinoma of the oesophagus', 'oesophagus adenocarcinoma', 'adenocarcinoma of oesophagus', 'oesophageal adenocarcinoma', 'adenocarcinoma of the esophagus', 'adenocarcinoma - oesophagus', 'adenocarcinoma - esophagus', 'adenocarcinoma of esophagus']",4914,,99976,C0279628,,C4025,0000478,,,,,
mondo:0005029,essential thrombocythemia,"['essential thrombocythaemia', 'ET', 'essential thrombocytemia', 'essential thrombocytosis', 'essential thrombocythemia', 'primary thrombocytosis', 'idiopathic thrombocythemia', 'primary thrombocythemia', 'hemorrhagic thrombocythemia']",2224,,71493,C0040028,"['-0.3267', '-0.4397', '-0.799', '0.2123', '-0.08954', '-0.1193', '0.003448', '0.871', '-0.176', '-0.2502', '0.03516', '-0.2817', '0.2244', '0.02942', '0.1643', '0.4363', '-0.51', '0.3157', '0.1804', '-0.67', '0.166', '-0.301', '1.0205', '0.0791', '0.3193', '-0.002993', '0.06805', '-0.2695', '-0.1418', '0.264', '0.0992', '-0.2133', '0.2375', '0.2856', '-0.012665', '-0.02487', '-0.4841', '-0.257', '0.6045', '-0.4062', '0.1172', '-0.03732', '0.3948', '-0.2362', '0.2612', '-0.0724', '-0.5293', '0.4614', '0.4802', '-0.1015', '0.337', '0.3042', '0.5493', '-0.1176', '-0.2593', '0.269', '-0.1498', '-0.3752', '-0.737', '0.1317', '-0.3926', '0.546', '0.2878', '-0.6675', '0.09155', '0.57', '0.3625', '0.2996', '-0.3167', '0.9463', '-0.02728', '-0.263', '-0.1898', '-0.4658', '0.3225', '0.393', '0.1477', '0.823', '0.7437', '0.1875', '-0.7754', '-0.2896', '0.1936', '-0.5034', '-0.2173', '-0.322', '0.4224', '0.3638', '0.3997', '-0.0722', '0.5063', '-0.2827', '-0.575', '-0.1885', '0.1362', '0.6675', '0.01337', '-0.8535', '-0.3137', '0.1705']",C3407,0000479,D013920,238.71,,10015493,
mondo:0005030,fetal growth restriction,"['fetal SGA', 'fetal small for gestational Age', 'fetus small for gestational Age', 'foetal small for gestational Age', 'intrauterine Growth restriction', 'foetal Growth retardation', 'IUGR', 'foetal growth retardation', 'fetal Growth retardation', 'foetus small for gestational Age', 'intrauterine Growth retardation', 'fetal growth retardation', 'foetal SGA']",,,,,,C114875,0000495,D005317,764.99,,,
mondo:0005031,fibromatosis,['fibromatosis'],,,,,"['-0.1724', '0.10626', '0.0981', '-0.1676', '0.1284', '-0.084', '0.000651', '-0.03912', '-0.03735', '0.04398', '-0.12256', '0.10364', '0.01246', '0.04352', '-0.274', '-0.0363', '0.05823', '-0.1804', '-0.03214', '-0.4226', '-0.04166', '-0.1632', '0.3', '-0.1722', '0.0596', '-0.00958', '-0.0959', '0.008156', '-0.01058', '-0.2076', '0.1497', '0.0162', '0.04742', '-0.0627', '0.0088', '0.05005', '-0.2065', '0.0786', '0.03696', '-0.3572', '0.0698', '-0.2229', '0.02252', '-0.07904', '0.02516', '-0.1499', '0.04504', '0.08734', '0.2104', '0.01462', '0.06088', '-0.0719', '0.094', '0.1807', '-0.1948', '-0.1069', '0.1403', '0.02925', '-0.3713', '-0.06555', '0.1427', '0.1486', '-0.2054', '-0.0245', '0.004982', '0.0898', '0.2766', '0.183', '-0.1755', '0.1772', '-0.1875', '-0.02808', '0.1399', '0.05908', '-0.02232', '-0.00678', '-0.03784', '0.1387', '-0.1549', '-0.3398', '-0.2294', '-0.0579', '-0.004566', '0.0792', '-0.1598', '-0.131', '0.04565', '0.12195', '0.2161', '-0.0371', '0.0622', '0.3154', '-0.00542', '0.0318', '0.3167', '-0.010666', '0.1542', '-0.3447', '0.02075', '0.1147']",C3042,0000497,,,,,
mondo:0005032,follicular thyroid adenoma,"['thyroid adenoma', 'follicular adenoma of the thyroid', 'follicular adenoma of thyroid', 'thyroid follicular adenoma', 'follicular adenoma of the thyroid gland', 'thyroid adenoma (disease)', 'follicular adenoma', 'thyroid gland follicular adenoma', 'adenoma of the thyroid gland', 'adenoma of thyroid', 'follicular adenoma (morphologic abnormality)', 'follicular adenoma of thyroid gland', 'follicular thyroid adenoma', 'adenoma of the thyroid', 'thyroid gland adenoma', 'adenoma of thyroid gland', 'adenoma, follicular cell, benign']",6204,,,C0205647,,C3502,0000499,,,,,0000854
mondo:0005033,ganglioneuroma,"['GN', 'ganglioneuroma (Schwannian Stroma-dominant)', 'ganglioneuroma, benign', 'ganglioneuroma', 'ganglioneuroma (disease)', 'neural Crest tumor, benign']",4817,,251992,C0017075,,C3049,0000500,D005729,215.9,,10017709,0003005
mondo:0005034,thyroid gland follicular carcinoma,"['carcinoma, follicular cell, malignant', 'follicular adenocarcinoma, well differentiated (morphologic abnormality)', 'follicular adenocarcinoma, well differentiated', 'follicular carcinoma of thyroid gland', 'carcinoma of thyroid follicle', 'well-differentiated follicular adenocarcinoma', 'thyroid follicular carcinoma', 'follicular cancer of thyroid gland', 'thyroid gland adenocarcinoma', 'follicular carcinoma', 'follicular carcinoma of the thyroid gland', 'follicular cancer of thyroid', 'well-differentiated follicular carcinoma', 'follicular adenocarcinoma', 'thyroid gland follicular carcinoma', 'follicular carcinoma of the thyroid', 'follicular thyroid carcinoma', 'follicular thyroid cancer', 'follicular cancer of the thyroid gland', 'thyroid gland follicular cancer', 'follicular thyroid gland carcinoma', 'follicular cancer of the thyroid', 'follicular carcinoma of thyroid', 'follicular adenocarcinoma (morphologic abnormality)']",3962,,,,"['-0.1771', '0.246', '-0.1165', '0.0904', '0.1708', '0.3154', '0.2483', '0.09326', '0.09216', '-0.1617', '-0.0341', '0.1261', '-0.2285', '-0.2002', '-0.12195', '-0.2163', '0.0366', '-0.3113', '0.0918', '-0.2913', '0.2115', '-0.3005', '0.531', '-0.4607', '0.3538', '0.1882', '0.03217', '0.1122', '-0.1436', '-0.2903', '0.4353', '0.04288', '0.0451', '-0.033', '0.001298', '0.05865', '-0.163', '-0.0269', '0.0853', '-0.06476', '-0.02536', '0.0555', '0.1964', '-0.1192', '0.2039', '-0.1132', '0.0892', '0.03525', '0.1898', '-0.1909', '0.0985', '-0.1054', '0.0363', '0.193', '-0.3818', '-0.002705', '0.444', '-0.3914', '-0.4697', '-0.03027', '0.225', '0.2289', '-0.3887', '-0.006454', '-0.002491', '0.377', '0.312', '0.295', '-0.3257', '0.4866', '0.09625', '-0.01862', '0.244', '-0.1489', '0.2042', '-0.04102', '-0.1453', '-0.05502', '-0.04858', '-0.468', '-0.3977', '0.0824', '0.06714', '-0.275', '-0.4214', '-0.1752', '0.1869', '0.04395', '0.3127', '-0.2744', '0.253', '0.2167', '-0.1141', '-0.0864', '0.708', '-0.1608', '-0.0536', '-0.3716', '-0.1779', '-0.0614']",C8054,0000501,D018263,,,,0006731
mondo:0005035,ganglioneuroblastoma,"['ganglioneuroblastoma, malignant', 'ganglioneuroblastoma (morphologic abnormality)', 'ganglioneuroblastoma (disease)', 'ganglioneuroblastoma']",4163,,251877,C0206718,,C3790,0000502,D018305,171.9,,10017708,0006747
mondo:0005036,gastric adenocarcinoma,"['stomach adenocarcinoma', 'STAD', 'gastric adenocarcinoma', 'gastric (stomach) adenocarcinoma', 'adenocarcinoma of stomach', 'adenocarcinoma - stomach', 'adenocarcinoma of the stomach']",3717,,464463,C0278701,,C4004,0000503,,,,,
mondo:0005037,gastric intestinal type adenocarcinoma,"['intestinal adenocarcinoma of the stomach', 'intestinal adenocarcinoma of stomach', 'gastric intestinal type adenocarcinoma', 'intestinal gastric adenocarcinoma', 'intestinal stomach adenocarcinoma', 'gastric intestinal-type adenocarcinoma', 'intestinal type stomach adenocarcinoma']",,,,C0279633,,C9157,0000504,,,,,
mondo:0005039,reproductive system disorder,"['disease of reproductive system', 'reproductive system disorder', 'genital disorders', 'reproductive disease', 'reproductive system disease or disorder', 'reproductive system disease', 'genital system disease', 'disorder of reproductive system']",15,,,C0178829,,C4875,0000512,,,,,
mondo:0005040,germ cell tumor,"['tumor of the germ cell', 'germ cell tumor', 'germ cells tumors', 'tumor of germ cell', 'malignant tumour of the germ cell', 'germ cell neoplasm', 'neoplasm of the germ cell', 'germ cells tumours', 'tumour of germ cell', 'tumour of the germ cell', 'germ cell cancer', 'neoplasm of germ cell']",688,,,C0205851,,C3708,0000514,,,,,
mondo:0005041,glaucoma,"['glaucoma (disease)', 'glaucoma']",1686,,,C0017601,,C26782,0000516,D005901,365.9,H40-H42,,0000501
mondo:0005043,hyperplasia,"['hyperplasia', 'hyperplastic']",,,,,,C3113,0000536,D006965,,,,
mondo:0005044,hypertensive disorder,"['blood pressure, high', 'pressure, high blood', 'HTN', 'hypertension', 'blood pressure, increased', 'vascular hypertensive disorder', 'increased blood pressure', 'high blood pressure', 'hyperpiesia', 'hypertensive disease']",10763,,,C0020538,"['-0.1799', '-0.1067', '-0.3345', '0.1915', '0.05383', '-0.10834', '-0.02638', '0.5356', '-0.0501', '0.2404', '-0.01744', '-0.02527', '0.2507', '-0.0874', '-0.3489', '-0.3596', '-0.1384', '0.12354', '0.2172', '-0.3047', '0.03983', '-0.195', '0.146', '0.1515', '0.1696', '-0.0704', '0.01929', '0.03894', '-0.331', '0.1772', '0.266', '-0.0667', '0.3167', '-0.0339', '-0.0001644', '-0.1923', '-0.2351', '-0.2072', '0.3208', '-0.6753', '0.01252', '-0.0781', '0.2045', '-0.4988', '0.2118', '-0.216', '-0.11237', '0.554', '-0.1509', '-0.11066', '0.1124', '0.1423', '0.0646', '-0.0685', '-0.1929', '0.3604', '0.1606', '-0.34', '-0.5303', '-0.0843', '0.06097', '0.3887', '0.1459', '-0.281', '-0.01086', '0.05264', '0.249', '0.1823', '-0.4167', '0.2084', '0.004555', '0.1439', '0.11304', '-0.0638', '0.0809', '0.02379', '-0.129', '-0.0781', '-0.1942', '-0.04147', '-0.1558', '0.1421', '-0.2362', '-0.12396', '0.3438', '0.1868', '0.157', '0.08936', '0.193', '-0.06024', '0.1812', '-0.1838', '-0.1332', '-0.02768', '0.6143', '0.11816', '0.1968', '-0.1461', '-0.502', '0.09033']",C3117,0000537,D006973,997.91,I15,,0000822
mondo:0005045,hypertrophic cardiomyopathy,"['familial hypertrophic cardiomyopathy', 'hypertrophic obstructive cardiomyopathy', 'obstructive hypertrophic cardiomyopathy', 'hypertrophic subaortic stenosis']",11984,,217569,C0007194,"['0.4375', '-0.6733', '-0.10535', '0.513', '0.02727', '-0.4397', '0.809', '0.796', '-0.3672', '-0.4995', '0.447', '-0.4592', '-0.401', '0.4985', '-0.566', '0.2905', '-0.8906', '-0.1389', '-0.726', '-0.7964', '0.3425', '0.3452', '0.661', '-0.2515', '0.4236', '-0.3396', '0.3828', '0.289', '-0.0786', '-0.2329', '0.761', '-0.2717', '0.4958', '0.528', '0.133', '-0.4731', '-0.328', '-0.4626', '0.7104', '-0.5293', '0.0806', '0.618', '0.12427', '0.5903', '0.3186', '0.421', '0.2678', '0.77', '0.581', '-0.511', '-0.3306', '0.1937', '0.76', '-0.1821', '0.5073', '-0.4998', '-0.4485', '0.4006', '-0.713', '-0.3389', '0.2246', '0.4697', '0.3733', '-1.082', '-0.742', '0.3896', '0.2028', '0.4558', '-0.573', '0.1769', '-0.3513', '0.2622', '0.09973', '-0.2898', '-0.1631', '0.7505', '-0.0863', '-0.05197', '-0.4282', '0.3472', '0.11316', '-0.4429', '0.02171', '-0.3757', '1.091', '-0.2722', '0.4932', '-0.076', '0.646', '0.2289', '0.05765', '-0.01283', '-0.2883', '0.3123', '0.943', '0.975', '0.1702', '-0.5586', '-0.3452', '-0.1752']",C34449,0000538,D002312,425.4,I42.2,10020871,0001639
mondo:0005046,immune system disorder,"['disease of immune system', 'immune system disorder', 'disorder of immune system', 'immune dysfunction', 'immune disease', 'immune disorder', 'immune system disease or disorder']",2914,,,,"['-0.1903', '0.2603', '0.03766', '-0.00998', '0.072', '0.03378', '0.1376', '-0.228', '-0.1814', '-0.026', '0.1697', '-0.0858', '-0.01576', '-0.009285', '-0.1827', '-0.2211', '-0.172', '0.10876', '-0.3442', '-0.483', '0.2087', '-0.1721', '0.4714', '-0.3062', '0.0389', '-0.2944', '-0.2683', '-0.2532', '-0.08075', '-0.2942', '0.444', '0.1981', '0.2751', '0.00655', '0.002726', '0.05508', '-0.278', '0.01122', '-0.2588', '-0.1754', '0.02884', '-0.1774', '0.0382', '-0.10925', '0.1542', '-0.4001', '0.2905', '-0.1292', '0.3088', '0.1665', '-0.05222', '0.248', '0.2524', '0.1454', '-0.261', '-0.2568', '0.03333', '-0.01394', '-0.2617', '0.03595', '0.156', '0.14', '0.06274', '0.4473', '-0.04315', '0.1412', '0.15', '0.3684', '-0.469', '0.315', '-0.364', '0.01518', '0.0283', '0.07587', '0.1945', '0.1278', '0.05524', '0.2493', '-0.045', '-0.2505', '-0.2281', '-0.2876', '0.0848', '0.4094', '-0.03912', '-0.296', '0.4504', '0.013145', '0.007706', '0.0867', '0.1361', '0.2947', '0.05182', '-0.0974', '0.4075', '0.501', '0.2903', '-0.3635', '-0.1384', '0.2886']",C3507,0000540,D007154,279.9,,,
mondo:0005047,infertility disorder,"['fertility disorders', 'sterility', 'Sterile', 'sterile', 'infertile', 'infertility']",5223,,,,,C3836,0000545,D007246,,,,
mondo:0005048,pancreatic insulin-producing neuroendocrine tumor,"['pancreatic insulin producing tumour', 'insulin-producing tumour of islet cells', 'Beta cell tumor of the pancreas', 'pancreatic insulin-producing tumor', 'pancreatic insulin producing tumor', 'insulin-producing islet cell tumor', 'beta cell tumour of the pancreas', 'Beta cell tumor of pancreas', 'insulin-producing tumour of the islet cells', 'pancreatic insulin producing neoplasm', 'pancreatic insulin-producing neuroendocrine tumor', 'beta cell tumor of the pancreas', 'insulin-producing tumor of the islet cells', 'beta cell neoplasm', 'Beta cell tumour of the pancreas', 'Beta cell tumor', 'insulin-producing tumor of islet cells', 'pancreatic Beta cell tumour', 'Beta cell tumour', 'pancreatic Beta cell tumor', 'pancreatic insulin-producing tumour', 'Beta cell tumour of pancreas', 'insulin-producing islet cell tumour', 'pancreatic insulin producing NET']",,,97279,,,C3140,,,,,,
mondo:0005050,invasive ductal and lobular carcinoma,"['invasive duct and lobular carcinoma', 'invasive ductal and lobular carcinoma', 'infiltrating ductal and lobular carcinoma']",,,,C1334277,,C7688,0000552,,,,,
mondo:0005051,invasive lobular breast carcinoma,"['invasive lobular carcinoma', 'invasive lobular carcinoma of breast', 'lobular carcinoma (morphologic abnormality)', 'infiltrating lobular breast carcinoma', 'infiltrating lobular carcinoma of breast', 'invasive lobular carcinoma, classic type', 'invasive lobular breast carcinoma', 'lobular carcinoma of the breast', 'infiltrating lobular carcinoma of the breast', 'infiltrating lobular adenocarcinoma', 'invasive lobular carcinoma of the breast', 'lobular carcinoma', 'lobular carcinoma NOS (morphologic abnormality)', 'breast invasive lobular carcinoma', 'classic invasive lobular carcinoma', 'invasive lobular adenocarcinoma']",3457,,,C0279565,,C7950,0000553,,,,,
mondo:0005052,irritable bowel syndrome,"['irritable colon', 'IBD', 'irritable bowel syndrome', 'psychogenic IBS', 'spastic colon', 'mucus colitis', 'IBS']",9778,,,C0022104,,C82343,0000555,D043183,564.1,K58,,
mondo:0005053,ischemic disease,['ischemia'],326,,,,,C34738,0000556,D054058,,,,
mondo:0005055,Kaposi^s sarcoma,"['anal Kaposi^s sarcoma', 'Kaposi^s sarcoma of soft tissues', 'Kaposi^s sarcoma of cornea', 'Kaposi^s sarcoma of esophagus', 'Kaposi^s sarcoma of skin', 'Kaposi^s sarcoma of lung', 'Kaposi^s sarcoma of central nervous system', 'Kaposi^s sarcoma of penis', 'Kaposi^s sarcoma of palate', 'Kaposi^s sarcoma, lung', 'Kaposi^s sarcoma of soft tissue', 'gastric Kaposi^s sarcoma', 'lymphadenopathic Kaposi^s sarcoma', 'KS', 'cardiac Kaposi^s sarcoma', 'Mediterranean Kaposi sarcoma', 'conjunctival Kaposi^s sarcoma', 'Kaposi^s sarcoma of conjunctiva', 'Kaposi^s sarcoma-associated herpesvirus (KSHV)', 'soft tissue Kaposi^s sarcoma', 'Kaposi^s sarcoma', 'Kaposi^s sarcoma (disease)', 'Kaposi^s sarcoma of the prostate', 'Kaposi^s sarcoma of heart', 'Kaposi^s sarcoma of anus', 'African lymphadenopathic Kaposi^s sarcoma', 'Kaposi^s sarcoma of gastrointestinal sites', 'penis Kaposi^s sarcoma', 'esophageal Kaposi^s sarcoma', 'prostate Kaposi^s sarcoma', 'pulmonary Kaposi^s sarcoma', 'multiple hemorrhagic sarcoma', 'Kaposi^s sarcoma of the gallbladder', 'Kaposi^s sarcoma of oesophagus', 'central nervous system Kaposi^s sarcoma', 'HHV8', 'Kaposi^s sarcoma of the CNS', 'cutaneous Kaposi^s sarcoma', 'non AIDS related Kaposi sarcoma', 'Kaposi sarcoma herpesvirus', 'KSHV', 'intestinal Kaposi^s sarcoma', 'corneal Kaposi^s sarcoma', 'Kaposi sarcoma', 'Kaposi^s sarcoma, skin', 'gallbladder Kaposi^s sarcoma', 'lymph node Kaposi^s sarcoma', 'human herpesvirus 8', 'palate Kaposi^s sarcoma', 'Kaposi^s sarcoma of lymph nodes']",8632,,33276,,"['-0.0963', '-0.4807', '-0.0531', '-0.1979', '0.0449', '-0.305', '0.6475', '-0.04086', '-0.1702', '-0.672', '0.3184', '0.11316', '-0.0981', '0.2102', '-0.0761', '0.164', '-0.3352', '-0.4436', '-0.1833', '-0.515', '-0.1592', '-0.4155', '0.7725', '-0.1993', '-0.0903', '-0.3245', '-0.2195', '-0.602', '-0.6104', '-0.2056', '1.025', '-0.4226', '0.2457', '-0.2593', '0.1663', '0.3865', '-0.747', '-0.08014', '0.01131', '-0.12', '0.3516', '-0.664', '-0.0744', '-0.2966', '0.532', '0.262', '-0.51', '-0.4849', '0.3955', '-0.7646', '0.07056', '-0.2747', '0.8574', '0.01339', '-0.2527', '0.5957', '-0.2769', '0.3484', '-0.328', '-0.5273', '0.2025', '0.63', '-0.4216', '-0.02147', '0.2458', '0.2285', '0.5625', '-0.10596', '0.04987', '0.93', '-0.2979', '0.1329', '-0.1371', '0.5576', '0.88', '0.203', '-0.09534', '-0.05508', '0.02936', '-0.3872', '-0.88', '-0.4895', '0.0871', '0.05066', '-0.464', '-0.3335', '0.54', '0.0285', '-0.05707', '-0.12054', '0.0888', '0.0535', '-0.454', '0.01218', '0.8687', '0.2485', '0.127', '-0.7334', '0.1892', '-0.571']",C9087,0000558,D012514,176.9,,10023284,0100726
mondo:0005056,keratinizing squamous cell carcinoma,"['keratinizing squamous cell carcinoma', 'keratinizing epidermoid carcinoma', 'squamous cell carcinoma, keratinizing (morphologic abnormality)', 'squamous cell carcinoma, keratinizing']",5521,,,C0334247,,C4105,0000559,,,,,
mondo:0005057,large cell neuroendocrine carcinoma,"['large cell NEC', 'large cell neuroendocrine carcinoma', 'LCNEC', 'large-cell neuroendocrine carcinoma']",0050872,,,C1265996,,C6875,0000563,,,,,
mondo:0005058,leiomyosarcoma,"['leiomyosarcoma', 'Leiomyosarcomas', 'leiomyosarcoma (excluding uterine leiomyosarcoma)', 'leiomyosarcoma - not uterine', 'leiomyosarcoma, malignant']",1967,,64720,C0023269,"['-0.5684', '-0.3535', '0.3108', '-0.04562', '0.4382', '-0.5264', '0.541', '-0.4097', '0.08374', '-0.5176', '-0.0169', '0.4827', '-0.1564', '0.2496', '-0.5347', '-0.03494', '-0.3132', '-0.414', '-0.07544', '-0.6665', '-0.003746', '-0.2107', '0.524', '-0.1545', '0.3093', '-0.1991', '-0.1519', '-0.316', '-0.4993', '0.135', '0.7026', '-0.1345', '0.7266', '-0.5527', '0.2969', '0.4683', '-1.02', '0.4165', '-0.0429', '-0.41', '-0.04535', '-0.1908', '-0.2817', '-0.06052', '0.5674', '0.0354', '-0.2194', '-0.3005', '0.892', '-0.4556', '0.127', '-0.2852', '0.0809', '0.10706', '-0.0679', '-0.1978', '-0.2542', '0.576', '-0.4795', '-0.3574', '0.1919', '0.348', '-0.4058', '-0.1271', '-0.388', '0.2715', '0.5635', '0.1295', '0.2104', '0.856', '-0.3674', '0.4912', '-0.3582', '0.1959', '0.4453', '0.2637', '-0.1384', '0.727', '0.04', '-0.8086', '-0.8716', '0.146', '-0.1877', '0.08813', '-0.849', '-0.4343', '0.4255', '0.1256', '0.2285', '-0.00986', '-0.00461', '-0.0233', '-0.4197', '0.05704', '0.5664', '0.1852', '0.1926', '-0.815', '-0.528', '-0.4995']",C3158,0000564,D007890,171.9,,10024189,
mondo:0005059,leukemia,"['leukaemia NOS', 'leukemia', 'leukemias', 'blood (leukemia)', 'leukemia, disease', 'leukemia, malignant', 'leukaemia (disease)', 'leukemia (disease)', 'leukemias, general']",1240,,,C0023418,,C3161,0000565,D007938,208.90,,,0001909
mondo:0005060,liposarcoma,"['sarcoma of lip', 'liposarcoma, malignant', 'lip sarcoma', 'liposarcoma']",3382,,69078,C0023827,,C3194,0000569,D008080,171.9,,10024627,
mondo:0005061,lung adenocarcinoma,"['adenocarcinoma of lung', 'adenocarcinoma of the lung', 'nonsmall cell adenocarcinoma', 'bronchogenic lung adenocarcinoma', 'non-small cell lung adenocarcinoma', 'lung adenocarcinoma']",3910,,415268,C0152013,"['-0.2869', '-0.05783', '-0.4116', '0.04852', '0.1365', '-0.148', '0.2703', '0.2107', '0.1045', '-0.0817', '0.04922', '0.1799', '-0.1842', '0.1868', '-0.2983', '0.0467', '-0.0372', '0.10724', '0.0648', '-0.2329', '-0.12244', '-0.07635', '0.306', '-0.1698', '0.185', '-0.3296', '0.1696', '0.2617', '0.0717', '-0.1772', '0.466', '-0.1532', '0.3882', '-0.2625', '0.05902', '-0.3337', '-0.2245', '0.01546', '0.1708', '-0.0696', '-0.00918', '-0.1774', '0.2124', '-0.3418', '0.2091', '0.02763', '-0.3762', '0.07043', '0.0821', '0.2291', '-0.00526', '-0.1505', '-0.11084', '0.3372', '-0.2578', '0.1512', '-0.0665', '-0.05975', '-0.4473', '-0.3508', '0.2542', '0.2397', '0.05957', '0.004242', '0.08325', '0.1412', '0.4326', '0.3977', '-0.1327', '0.5615', '-0.1333', '0.02208', '0.2286', '-0.0736', '0.0442', '0.05283', '-0.1553', '-0.11505', '0.0422', '-0.3425', '-0.2268', '0.1528', '-0.03412', '-0.08716', '-0.2837', '-0.06744', '0.1472', '-0.09283', '0.06076', '-0.3894', '0.08057', '0.10913', '-0.1854', '0.0927', '0.5693', '0.02078', '-0.01076', '-0.1731', '-0.542', '-0.08624']",C3512,0005288,C538231,,,,
mondo:0005062,lymphoma,"['lymphoma (Hodgkin^s and non-Hodgkin^s)', 'lymphoid cancer', 'lymphoma, malignant', 'lymphoma', 'lymphoma (Hodgkin and non-Hodgkin)', 'malignant lymphoma', 'lymphomatous', 'MLYM']",0060058,,223735,C0024299,"['-0.353', '0.12396', '0.1627', '-0.255', '-0.1172', '-0.3264', '0.4517', '0.742', '-0.11017', '-0.1986', '0.5054', '0.4514', '-0.8774', '0.05377', '-0.2192', '0.09283', '-0.8125', '-0.0316', '-0.486', '-0.2019', '-0.2324', '0.00559', '0.2196', '-0.05237', '0.3489', '0.05304', '0.0503', '-0.3325', '-0.4417', '-0.379', '0.22', '0.3252', '0.7295', '-0.2498', '0.833', '0.08417', '-1.541', '0.3972', '0.0396', '-0.3926', '0.0182', '0.001157', '-0.12384', '-0.4316', '-0.03268', '-0.06058', '-0.5083', '-0.10284', '0.97', '0.02664', '-0.16', '0.05298', '0.4414', '0.2861', '-0.556', '0.10675', '-0.2013', '-0.193', '-0.274', '-0.4153', '0.3494', '0.2402', '0.1177', '-0.1879', '-0.1431', '0.2498', '0.4685', '0.623', '0.2178', '1.327', '-0.0257', '0.3765', '-0.513', '-0.442', '0.1936', '-0.0633', '-0.266', '0.908', '0.3118', '-0.1783', '-0.508', '-0.08154', '-0.06076', '-0.1311', '-0.4312', '-0.3135', '0.3774', '-0.2617', '0.4492', '0.1368', '0.3777', '-0.3555', '-0.002838', '-0.08203', '0.6016', '0.693', '-0.3123', '-0.291', '-0.705', '-0.2074']",C3208,0000574,D008223,202.80,,10025310,
mondo:0005063,medullary breast carcinoma,"['invasive medullary breast carcinoma', 'infiltrating medullary carcinoma of breast', 'medullary breast carcinoma with lymphoid Stroma', 'breast medullary carcinoma', 'invasive medullary carcinoma of breast', 'medullary carcinoma of the breast', 'medullary carcinoma of breast', 'invasive medullary carcinoma of the breast', 'infiltrating medullary carcinoma of the breast', 'medullary breast carcinoma', 'medullary breast cancer']",5605,,,C0860580,,C9119,0000580,,,,,
mondo:0005065,mesothelioma,['mesothelioma'],,,,C0025500,"['0.06757', '-0.11395', '-0.06476', '0.05988', '0.1971', '-0.0054', '0.0235', '0.2659', '-0.5103', '-0.1617', '0.888', '0.3828', '-0.399', '0.1024', '-0.0362', '-0.1054', '-0.8296', '-0.7144', '-0.2952', '-0.2568', '0.1501', '-0.6753', '0.3276', '-0.2676', '0.00954', '-0.6035', '-0.1848', '0.4453', '0.208', '-0.0507', '0.2477', '-0.2986', '0.6953', '-0.1821', '0.417', '-0.2708', '-0.92', '0.4272', '0.814', '-0.4949', '-0.10974', '0.1515', '0.5117', '-0.415', '-0.2417', '0.0719', '-0.03436', '0.09424', '1.024', '-0.1076', '-0.04565', '-0.7695', '0.1466', '-0.001553', '0.2318', '0.4949', '-0.2148', '0.469', '-0.78', '-0.5815', '0.5835', '0.2974', '-0.403', '0.2231', '-0.4265', '0.6733', '0.3054', '0.568', '-0.608', '1.085', '-0.127', '0.258', '-0.1519', '-0.3994', '0.722', '0.6284', '-0.4082', '0.4893', '0.195', '-0.2299', '-0.3997', '0.5645', '-0.296', '0.1274', '0.00635', '-0.12115', '0.355', '0.5435', '0.5425', '0.0699', '-0.4111', '-0.806', '-0.897', '0.95', '0.995', '-0.00659', '-0.3816', '-0.3245', '-0.6997', '-0.0683']",C3234,0000588,D008654,,C45,,
mondo:0005066,metabolic disease,"['metabolic process disease', 'disorder of metabolic process', 'metabolic disease', 'metabolic disorder', 'disease of metabolism']",0014667,,,C0025517,,C3235,0000589,D008659,277.9,E70-E88,,
mondo:0005067,monophasic synovial sarcoma,"['monophasic sarcoma of the synovium', 'monophasic synovial sarcoma', 'monophasic sarcoma of synovium']",5495,,,C1334801,,C6534,0000595,,,,,
mondo:0005068,myocardial infarction,"['myocardial infarction', 'myocardial infarct', 'myocardial infarction, (MI)', 'MI', 'myocardial infarction (disease)', 'heart attack', 'infarction (MI), myocardial', 'MI, myocardial infarction']",5844,,,C0027051,"['0.04605', '0.3171', '-0.3586', '0.6055', '0.3171', '-0.721', '0.07855', '-0.002113', '-0.3044', '-0.5107', '0.409', '-0.02414', '0.4265', '0.1635', '-0.6206', '-0.3652', '-0.75', '0.111', '-0.354', '-0.258', '0.4072', '0.444', '0.0973', '-0.1016', '-0.0745', '-0.7456', '0.2369', '0.4607', '0.0568', '-0.224', '0.707', '0.04913', '0.509', '0.06335', '-0.394', '-0.2542', '-0.0825', '0.05084', '0.515', '-0.544', '0.3718', '0.01562', '0.6807', '-0.1172', '0.3452', '-0.09064', '-0.1672', '-0.1123', '0.299', '0.2332', '0.01417', '0.3557', '0.828', '0.0948', '-0.1818', '0.0624', '-0.4592', '0.2219', '-0.2046', '-0.3184', '-0.841', '0.7812', '0.00855', '-0.4421', '-0.8574', '0.3113', '0.1952', '0.566', '-0.2164', '0.1511', '0.144', '-0.03214', '0.1284', '-0.694', '0.2361', '0.497', '0.2279', '0.5757', '-0.1252', '0.5283', '-0.3367', '-0.171', '-0.1567', '-0.01852', '0.3462', '-0.0413', '-0.05603', '0.367', '0.566', '0.1694', '-0.1063', '-0.07336', '-0.2815', '0.652', '0.7144', '0.2103', '-0.3833', '-0.714', '-0.6143', '0.02962']",C27996,0000612,D009203,,I21,,0001658
mondo:0005070,neoplasm,"['neoplastic growth', 'other neoplasm', 'tumor', 'tumour disease', 'neoplasm (disease)', 'disease of cellular proliferation', 'neoplastic disease', 'tumour', 'neoplasm', 'neoplasia', 'cell process disease']",14566,,,CN236628,,C3262,0000616,D009369,239.9,C7B-C7B,,0002664
mondo:0005071,nervous system disorder,"['neurologic disorder', 'neurological disease', 'neurological disorder', 'disease of nervous system', 'nervous system disease', 'nervous system disorder', 'nervous system disease or disorder', 'neurologic disease', 'disorder of nervous system']",863,,,C0027765,,C26835,0000618,D009422,349.9,G00-G99,,
mondo:0005072,neuroblastoma,"['neuroblastoma', 'neuroblastoma (Schwannian Stroma-poor)', 'neural Crest tumor, malignant', 'NB', 'neuroblastoma, malignant']",769,,635,CN205405,"['-0.09235', '0.2925', '0.2817', '-0.1838', '-0.10254', '0.2084', '0.14', '0.7', '-0.691', '-0.2139', '0.04776', '-0.2925', '-0.413', '0.3354', '-0.4517', '0.149', '-0.8433', '-0.8916', '0.3606', '-0.29', '0.3005', '-0.951', '0.11926', '-0.724', '-0.002922', '-0.0802', '0.4163', '0.4812', '-0.01778', '-0.02077', '0.2976', '-0.01519', '0.7534', '-0.09', '-0.145', '0.5005', '-1.054', '0.3481', '-0.4983', '0.01238', '0.2391', '-0.04184', '0.2708', '-0.7515', '-0.3958', '0.0225', '-0.314', '-0.4487', '0.4832', '-0.05334', '0.0918', '-0.3792', '0.00935', '0.04883', '-0.3582', '-0.1335', '-0.358', '0.1012', '0.01955', '-0.348', '0.4158', '0.182', '-0.4417', '0.0925', '-0.1608', '0.3975', '0.2527', '-0.1238', '0.657', '0.7266', '0.2069', '0.444', '0.00933', '-0.4695', '0.6416', '0.8276', '0.0418', '0.589', '0.04837', '-0.856', '-0.3271', '-0.186', '0.1407', '-0.39', '-0.4153', '-0.197', '1.135', '0.363', '0.2747', '0.5034', '0.1209', '-0.7246', '-0.1597', '0.2678', '1.132', '-0.2355', '0.2448', '-0.3691', '0.2573', '-0.0005465']",C3270,0000621,D009447,,,10029260,
mondo:0005073,melanocytic nevus,"['nevus', 'mole', 'mole of skin', 'melanocytic Nevus', 'melanotic Nevus']",,,,,"['-0.1263', '0.1547', '0.03296', '0.01276', '0.2524', '-0.1453', '-0.0853', '0.1131', '-0.147', '0.03244', '0.01087', '0.1439', '0.03162', '0.0425', '-0.1908', '-0.002956', '0.04678', '-0.1877', '0.08563', '-0.3145', '-0.0777', '-0.0998', '0.135', '-0.07965', '0.06155', '-0.0588', '-0.0951', '-0.0524', '-0.07513', '-0.00488', '0.2445', '-0.1482', '0.1061', '-0.05426', '0.10693', '0.1084', '-0.0667', '0.03044', '0.0003002', '-0.2642', '0.1565', '-0.2598', '0.0347', '-0.10944', '-0.066', '-0.0878', '-0.0454', '0.077', '0.09827', '0.0781', '0.0218', '-0.002611', '0.0824', '0.1826', '-0.1161', '0.00515', '0.2507', '-0.02496', '-0.2842', '-0.08923', '0.09406', '0.05862', '-0.1387', '0.10913', '0.0911', '0.02644', '0.307', '0.1595', '-0.03235', '0.315', '-0.04327', '0.03412', '0.05072', '-0.03925', '-0.00769', '0.08875', '-0.08606', '0.0442', '-0.05078', '-0.351', '-0.04712', '-0.1026', '-0.04425', '0.0637', '-0.1188', '-0.1018', '-0.01924', '0.1012', '0.2094', '0.02881', '0.11395', '0.0938', '0.02023', '0.04092', '0.3083', '-0.03146', '0.09485', '-0.2002', '-0.0665', '-0.02434']",C7570,0000625,D009506,,,,
mondo:0005074,papillary cystadenocarcinoma,"['papillary cystadenocarcinoma', 'cystadenocarcinoma, papillary, malignant', 'papillary cystadenocarcinoma, NOS (morphologic abnormality)', 'papillary cystadenocarcinoma (morphologic abnormality)']",3110,,,C0206700,,C3777,0000639,D018283,,,,
mondo:0005075,thyroid gland papillary carcinoma,"['thyroid gland papillary carcinoma', 'papillary cancer of the thyroid gland', 'papillary carcinoma of the thyroid', 'papillary carcinoma of the thyroid gland', 'thyroid papillary carcinoma', 'papillary cancer of thyroid gland', 'papillary cancer of thyroid', 'papillary carcinoma of thyroid gland', 'papillary thyroid carcinoma', 'papillary thyroid gland carcinoma', 'papillary cancer of the thyroid', 'papillary carcinoma of thyroid', 'papillary thyroid cancer', 'thyroid gland papillary cancer']",3969,,,C0238463,"['-0.1989', '0.1214', '-0.0902', '0.08716', '0.1373', '0.3533', '0.222', '0.09937', '0.1508', '-0.013855', '-0.09827', '0.04974', '-0.01993', '-0.01267', '-0.2805', '-0.282', '-0.0527', '-0.4224', '0.1417', '-0.1957', '0.1124', '-0.14', '0.4734', '-0.2092', '0.4915', '0.0353', '0.03543', '-0.01174', '0.03085', '-0.3481', '0.4087', '-0.005306', '0.141', '-0.279', '0.1432', '0.07275', '-0.1409', '-0.1216', '0.1476', '-0.1087', '-0.0454', '0.04626', '0.05255', '-0.03363', '0.3232', '-0.3252', '0.05267', '-0.03864', '0.1495', '-0.02457', '0.03192', '-0.244', '-0.142', '0.2905', '-0.7964', '-0.10706', '0.3777', '-0.3655', '-0.3125', '0.04318', '0.3423', '0.1111', '-0.4482', '0.03105', '-0.02866', '0.4832', '0.2961', '0.3184', '-0.1193', '0.4563', '-0.05038', '0.1179', '0.2837', '-0.1322', '0.0983', '0.05978', '-0.06396', '-0.3262', '-0.2031', '-0.5083', '-0.2974', '0.00951', '-0.1755', '-0.155', '-0.4016', '-0.2401', '0.1759', '0.2379', '0.1182', '-0.2079', '-0.01454', '0.05484', '-0.1604', '0.06964', '0.71', '-0.1431', '0.07263', '-0.1525', '-0.10443', '-0.02014']",C4035,0000641,,,,,0002895
mondo:0005076,periodontitis,"['periodontium inflammation', 'chronic pericementitis', 'periodontosis']",9893,,,C0600298,"['0.9053', '-0.2395', '0.1906', '0.572', '0.4646', '-0.3926', '0.2401', '0.4133', '-0.3965', '0.7427', '-0.1786', '-0.556', '-0.35', '0.693', '-0.2136', '-0.1742', '-0.7144', '0.5996', '-0.544', '-1.191', '-0.2427', '-0.5425', '0.1395', '-0.3809', '-0.1761', '-0.522', '-0.9185', '-0.06635', '0.073', '-0.315', '-0.406', '0.2155', '-0.05057', '0.3904', '0.73', '0.842', '-0.02971', '0.1849', '0.7935', '-0.8696', '-0.1755', '0.2078', '-0.5615', '-0.04068', '0.0728', '0.05997', '-0.02223', '-0.1577', '0.04102', '-0.3237', '-0.07355', '0.21', '0.573', '0.0952', '-0.215', '-0.5874', '-0.435', '-0.2086', '-1.322', '-0.83', '-0.08453', '0.2383', '-0.2467', '-0.584', '-0.3162', '0.314', '0.6147', '-0.1053', '0.1132', '1.239', '0.2983', '-0.2556', '0.3604', '-0.866', '0.765', '0.01904', '-0.03021', '0.4539', '-0.1683', '-0.5537', '-0.7383', '-0.2756', '-0.15', '-0.02446', '0.5815', '-0.067', '0.1995', '-0.352', '0.8423', '-0.00967', '0.3938', '0.1313', '0.3435', '0.6094', '0.3103', '0.0933', '-0.54', '-1.034', '-0.3591', '-0.1172']",C34918,0000649,D010520,523.5,K05.4,,
mondo:0005077,pertussis,"['Bordetella pertussis infection', 'WC - whooping cough', 'pertussis', 'Bordetella pertussis caused disease or disorder', 'Bordetella infection', 'whooping cough']",1116,,1489,C0043167,,C85231,0000650,D014917,033.9,A37.1,10047974,
mondo:0005078,phyllodes tumor,"['cystosarcoma phyllodes', 'phyllodes neoplasm', 'CSP', 'phyllodes tumor']",,,,,,C2977,0000653,D003557,,,,
mondo:0005079,polyp,['polyp'],,,,,,C3340,0000662,D011127,,N84,,
mondo:0005080,portal hypertension,,10762,,,C0020541,"['-0.0678', '0.07184', '-0.074', '-0.1946', '-0.02493', '-0.2104', '0.1439', '0.04822', '-0.02307', '0.07025', '-0.306', '-0.31', '-0.0828', '0.0512', '-0.579', '-0.478', '-0.2964', '-0.0401', '-0.009636', '-0.4583', '0.1409', '-0.1733', '0.1532', '-0.1377', '0.01311', '-0.003819', '0.1619', '0.2634', '0.0804', '0.00347', '0.3218', '-0.11804', '0.4072', '-0.05777', '-0.12445', '-0.003729', '-0.2573', '-0.01846', '0.1456', '-0.2686', '-0.1794', '0.1257', '0.338', '-0.04727', '0.02797', '0.05075', '0.01881', '0.1411', '0.03796', '-0.00334', '-0.1704', '0.3367', '0.2186', '-0.03937', '-0.218', '0.0897', '0.02568', '-0.03748', '-0.3862', '0.0952', '0.1114', '0.2532', '-0.002197', '-0.2712', '-0.03778', '-0.1991', '0.211', '0.2568', '-0.4473', '0.3813', '-0.3083', '0.1586', '-0.005596', '-0.163', '-0.02812', '0.1001', '0.1404', '-0.075', '0.0431', '-0.02658', '-0.3003', '-0.011086', '-0.2214', '-0.01233', '0.1176', '0.04025', '0.3113', '-0.004925', '0.2286', '-0.2023', '-0.0358', '0.03198', '-0.10986', '-0.00397', '0.594', '0.3896', '0.298', '-0.12067', '-0.1085', '-0.012856']",C3119,0000666,D006975,572.3,K76.6,,
mondo:0005081,preeclampsia,"['hypertension induced by pregnancy', 'gestational hypertension', 'preeclampsia/eclampsia', 'pregnancy associated hypertension', 'pre-eclampsia', 'proteinuric hypertension of pregnancy', 'toxemia of pregnancy', 'pregnancy toxemia', 'preeclampsia', 'pregnancy toxaemia', 'toxaemia of pregnancy', 'pre-eclamptic toxemia', 'pre-eclamptic toxaemia']",10591,,275555,,"['0.1345', '-0.0972', '-0.268', '-0.09973', '0.5645', '-0.3833', '-0.006664', '0.9756', '-0.12445', '-0.02237', '-0.4133', '-0.2042', '0.413', '0.794', '-0.806', '-0.3977', '-0.3252', '0.2068', '0.3735', '-0.2477', '-0.1401', '-0.4126', '0.0872', '-0.1274', '0.167', '-0.2239', '0.04065', '0.5596', '0.3167', '0.03854', '0.586', '-0.6196', '0.808', '0.1498', '-0.4539', '0.1779', '-0.3025', '0.1647', '0.586', '-0.1049', '0.2625', '-0.0801', '0.3489', '-0.315', '0.2351', '-0.5347', '-0.2622', '-0.03894', '0.151', '-0.1464', '-0.03735', '0.02258', '0.2715', '-0.3843', '0.09656', '0.008156', '0.05792', '-0.0689', '0.06647', '0.01429', '-0.375', '-0.04834', '0.3198', '-0.002573', '-0.3838', '0.551', '0.2144', '0.33', '-0.587', '0.749', '0.5405', '0.5195', '0.414', '-0.3389', '0.1434', '0.5024', '-0.0005107', '0.658', '0.4673', '0.2744', '-0.4465', '0.07153', '-0.5474', '-0.1499', '0.2559', '-0.1497', '0.3264', '-0.1688', '0.7676', '0.0465', '0.1895', '0.02605', '-0.6973', '0.218', '0.54', '0.2522', '-0.3694', '-0.541', '-0.271', '0.3176']",C85021,0000668,D011225,642.44,,10036485,
mondo:0005082,prostate adenocarcinoma,"['prostate gland adenocarcinoma', 'prostate adenocarcinoma', 'prad', 'adenocarcinoma of the prostate', 'adenocarcinoma of prostate']",2526,,,C0007112,"['-0.2073', '0.1123', '-0.00134', '0.1002', '0.04297', '-0.0838', '0.069', '0.0663', '-0.0334', '-0.1338', '-0.0957', '0.007065', '-0.0941', '0.1566', '-0.227', '-0.1725', '-0.02182', '-0.0981', '0.0779', '-0.2379', '-0.06366', '-0.142', '0.10675', '-0.2015', '0.2183', '-0.119', '0.0718', '0.0406', '-0.0762', '-0.2615', '0.2344', '-0.009636', '0.0853', '-0.1112', '0.0809', '-0.05417', '-0.07086', '0.0789', '0.02063', '-0.1564', '0.02737', '-0.2041', '0.04434', '-0.191', '-0.09686', '-0.1342', '0.0038', '-0.04556', '0.1685', '0.03366', '0.03102', '0.02766', '0.014145', '0.1175', '-0.233', '0.01385', '0.213', '0.003735', '-0.3074', '-0.02289', '0.2476', '0.1544', '-0.0732', '0.05402', '0.00547', '0.11664', '0.329', '0.2786', '-0.138', '0.1842', '0.03888', '0.00917', '0.1423', '-0.0895', '0.04816', '-0.01191', '-0.01913', '0.04584', '-0.12494', '-0.1823', '-0.2825', '0.1299', '-0.06107', '-0.04126', '-0.2289', '-0.1566', '0.09985', '0.0196', '0.1785', '-0.1996', '0.01962', '0.2068', '0.02682', '-0.0433', '0.423', '-0.04684', '0.0798', '-0.2094', '-0.1616', '0.11957']",C2919,0000673,,,,,
mondo:0005083,psoriasis,,8893,,,C0033860,"['0.06464', '-0.12445', '-0.3584', '0.05258', '-0.2717', '-0.822', '0.1863', '-0.2573', '-0.2734', '-0.03842', '0.164', '0.8857', '-0.157', '0.4785', '-0.187', '0.2852', '0.63', '0.3354', '-0.03372', '-0.531', '-0.4893', '0.0389', '0.479', '-0.1891', '0.06143', '0.5674', '-0.5337', '0.2437', '-0.0857', '-0.263', '0.589', '-0.334', '-0.2522', '0.272', '-0.03018', '0.261', '-0.811', '-0.2041', '0.27', '-0.3472', '0.05438', '-0.2435', '-0.1918', '0.3442', '0.9565', '0.06015', '0.3645', '-0.0716', '0.1906', '0.2109', '-0.635', '0.05496', '0.3877', '-0.2944', '0.01836', '-0.3123', '-0.1731', '0.01645', '-0.7524', '-0.746', '-0.5522', '0.09344', '-0.10986', '0.4285', '0.176', '0.4673', '0.54', '0.7095', '-0.0485', '1.202', '-0.1636', '-0.2588', '0.556', '-0.1969', '-0.578', '0.6357', '-0.01659', '0.687', '-0.2048', '-0.6665', '-0.545', '-0.2494', '-0.7056', '-0.03036', '0.439', '0.00584', '-0.3262', '0.2903', '0.207', '0.891', '0.4658', '0.3113', '0.4514', '0.4282', '0.657', '0.4502', '-0.1915', '-0.51', '-0.2491', '-0.03754']",C3346,0000676,D011565,696.8,L40,,
mondo:0005084,mental disorder,"['disorder of mental process', 'mental process disease', 'mental or behavioral disorder', 'mental or behavioural disorder']",150,,,CN240636,,C2893,0000677,D001523,V11.9,,,
mondo:0005085,pterygium,"['surfer^s eye', 'pterygium of conjunctiva and cornea']",0002116,,,C0033999,,C133744,0000678,D011625,372.40,H11.0,,
mondo:0005086,renal cell carcinoma,"['RCC', 'renal cell carcinoma (disease)', 'renal cell carcinoma', 'kidney adenocarcinoma', 'renal cell adenocarcinoma', 'hypernephroma']",4450,,217071,,"['-0.1165', '0.1826', '0.001276', '0.09845', '0.03644', '-0.1136', '-0.01082', '0.1333', '0.01997', '-0.0762', '-0.05765', '-0.1593', '-0.1134', '0.1398', '-0.3008', '-0.1927', '-0.06854', '-0.1396', '0.2096', '-0.2734', '-0.052', '-0.1359', '0.2126', '-0.1519', '0.2146', '-0.1364', '0.0263', '0.0626', '-0.0954', '-0.0985', '0.2028', '-0.007423', '0.1923', '-0.0755', '0.02553', '-0.1326', '-0.08386', '0.03723', '-0.00937', '-0.177', '-0.11475', '-0.2043', '0.1378', '-0.1432', '-0.0637', '-0.1093', '-0.0855', '-0.0666', '0.0977', '-0.08325', '0.0849', '0.02626', '0.1005', '0.0713', '-0.2004', '-0.10547', '0.2256', '0.01258', '-0.3516', '-0.03143', '0.2157', '0.03638', '-0.04327', '0.0002342', '0.1455', '0.05017', '0.3398', '0.2399', '-0.1622', '0.2222', '0.0317', '-0.0338', '0.1294', '-0.0114', '0.02112', '-0.01041', '-0.0461', '0.02878', '-0.0742', '-0.2327', '-0.2632', '0.11035', '-0.06287', '-0.00821', '-0.2129', '-0.1504', '0.07355', '0.03775', '0.191', '-0.0997', '0.06476', '0.1978', '0.03543', '-0.05356', '0.324', '0.0451', '0.1306', '-0.287', '-0.1675', '0.1688']",C9385,0000681,D002292,189.0,,10067946,0005584
mondo:0005087,respiratory system disorder,"['disorder of respiratory system', 'respiratory system disorder', 'respiratory system disease or disorder', 'respiratory system disease', 'respiratory disorder', 'respiratory disease', 'disease of respiratory system']",1579,,,,,C26871,0000684,D012140,V47.2,J00-J99,,
mondo:0005089,sarcoma,"['sarcoma, malignant', 'sarcoma of the soft tissue and bone', 'tumor of soft tissue and skeleton', 'tumour of soft tissue and skeleton', 'sarcoma', 'mesenchymal tumor, malignant', 'sarcoma of soft tissue and bone']",1115,,,,,C9118,0000691,D012509,171.9,,,
mondo:0005090,schizophrenia,"['schizophrenia-1', 'schizophrenia', 'SCZD', 'schizoaffective disorder', 'schizophrenia with or without an affective disorder', 'schizophrenia 12', 'schizophrenia (disease)', 'schizophrenia, susceptibility to']",5419,181500,3140,,"['0.416', '0.369', '-0.1598', '0.777', '-0.3325', '-0.459', '0.3513', '0.654', '-0.106', '-0.254', '0.4895', '-0.5415', '0.05707', '0.957', '0.1008', '-0.0678', '-0.637', '0.09283', '-0.34', '-0.929', '-0.5044', '-0.1664', '0.1729', '-0.307', '0.1635', '-0.304', '-0.071', '0.2952', '-0.1371', '-0.3967', '-0.09564', '-0.2534', '0.567', '0.3718', '-0.1123', '-0.05652', '-0.646', '0.0679', '0.1663', '-0.5396', '1.039', '-0.01371', '-0.371', '0.1954', '0.732', '-0.5356', '0.2876', '-0.5684', '0.0867', '0.472', '0.0581', '0.3113', '-0.302', '-0.1703', '0.6523', '0.53', '-0.4277', '0.02841', '-0.04193', '-0.3042', '-0.629', '0.333', '0.12286', '0.505', '-0.2634', '0.545', '0.382', '0.1805', '-0.5415', '0.7197', '0.1282', '-0.11694', '0.02065', '-0.2678', '0.1965', '0.705', '-0.0935', '1.103', '-0.1343', '-0.2089', '0.2345', '-0.4207', '-0.0717', '0.615', '0.2394', '0.0649', '-0.282', '0.0497', '0.606', '0.682', '0.179', '0.4937', '-0.38', '0.418', '-0.351', '0.1714', '-0.2842', '-0.666', '0.4019', '0.07635']",C3362,0000692,,295.90,,,0100753
mondo:0005091,severe acute respiratory syndrome,"['SARS-CoV infection', 'SARS coronavirus caused disease or disorder', 'SARS']",2945,,140896,C1175175,,C85064,0000694,D045169,079.82,,10061982,
mondo:0005092,signet ring cell carcinoma,"['signet ring carcinoma NOS (morphologic abnormality)', 'signet ring cell carcinoma (morphologic abnormality)', 'signet ring carcinoma', 'signet ring cell adenocarcinoma', 'signet ring cell carcinoma']",3493,,,C0206696,,C3774,0000698,D018279,,,,
mondo:0005093,skin disorder,"['skin diseases and manifestations', 'dermatosis', 'disorder of zone of skin', 'disease of zone of skin', 'genodermatosis', 'zone of skin disease or disorder', 'disorder of skin', 'zone of skin disease', 'cutaneous disorder', 'skin disorder', 'skin and subcutaneous tissue disease']",37,,,,,C3371,0000701,D012871,709.8,,,
mondo:0005094,hemangiopericytoma,"['hemangiopericytoma, malignant (morphologic abnormality)', 'hemangiopericytoma', 'malignant hemangiopericytoma', 'haemangiopericytic meningioma', 'haemangiopericytic meningioma [obs]']",264,,,,,C3087,,D006393,,,,
mondo:0005095,spondyloarthropathy,"['spondylarthrosis', 'spondyloarthritis', 'seronegative spondyloarthropathy', 'spondylarthropathy', 'spondarthropathy']",1123,,,,"['0.106', '0.007725', '0.03824', '-0.2064', '-0.0154', '-0.3916', '0.439', '-0.1449', '-0.2382', '-0.027', '-0.222', '-0.0922', '-0.02863', '0.5186', '-0.1721', '0.0668', '-0.0917', '0.0943', '0.006584', '-0.2164', '-0.00633', '-0.2435', '0.474', '-0.1454', '-0.2474', '0.1392', '0.08234', '-0.221', '0.11774', '0.0286', '0.04068', '-0.1595', '0.3154', '0.329', '0.2751', '0.1552', '-0.3765', '-0.1978', '-0.03815', '-0.3782', '-0.3152', '-0.5557', '-0.07404', '0.2098', '0.3362', '-0.2299', '-0.01889', '0.1571', '0.0536', '0.6357', '-0.0835', '0.12134', '0.1492', '0.0722', '-0.08826', '-0.3894', '0.05267', '-0.2615', '-0.1445', '-0.2297', '0.0893', '-0.07623', '-0.2207', '0.229', '-0.2432', '-0.2198', '0.1588', '0.5513', '0.1941', '0.421', '-0.3228', '-0.1199', '0.01005', '-0.421', '0.1012', '0.4395', '0.07855', '0.4763', '-0.1873', '-0.335', '-0.4177', '-0.1986', '-0.09796', '0.3584', '-0.05338', '-0.1692', '-0.0805', '0.05548', '-0.005672', '-0.1919', '0.3474', '0.07745', '0.128', '0.2556', '0.4514', '0.1936', '0.4136', '-0.03049', '-0.01753', '-0.2988']",C116778,0000706,D055009,,,,
mondo:0005096,squamous cell carcinoma,"['squamous cell epithelioma', 'malignant squamous cell tumour', 'squamous cell carcinoma NOS (morphologic abnormality)', 'squamous cell carcinoma (morphologic abnormality)', 'squamous carcinoma', 'malignant squamous cell neoplasm', 'carcinoma, squamous cell, malignant', 'epidermoid carcinoma', 'malignant epidermoid cell tumour', 'epidermoid cell cancer', 'malignant squamous cell tumor', 'squamous cell cancer', 'squamous cell carcinoma', 'malignant epidermoid cell neoplasm', 'malignant epidermoid cell tumor']",1749,,,C0007137,,C2929,0000707,D002294,,,,
mondo:0005097,squamous cell lung carcinoma,"['lung squamous cell carcinoma', 'squamous cell lung cancer', 'epidermoid cell carcinoma of lung', 'epidermoid cell lung carcinoma', 'squamous cell carcinoma of the lung', 'epidermoid cell carcinoma of the lung', 'squamous cell carcinoma of lung', 'squamous cell lung carcinoma']",3907,,,C0149782,,C3493,0000708,,162.9,,,
mondo:0005098,stroke disorder,"['stroke', 'cerebrovascular accident', 'cerebrovascular accident, (CVA)', 'stroke syndrome', 'CVA, cerebrovascular accident', 'CVA', 'syndrome, stroke', 'undetermined stroke', 'cerebral infarction']",,,,,"['-0.03958', '0.01703', '-0.5557', '0.4011', '-0.08575', '-0.5137', '0.322', '0.2864', '-0.2664', '-0.6997', '-0.1659', '-0.2391', '0.7896', '0.563', '0.005318', '-0.5996', '-0.2275', '0.2427', '-0.0731', '-0.3025', '0.1614', '0.04962', '-0.691', '0.1779', '-0.2332', '-0.6187', '-0.195', '0.04828', '0.1661', '-0.02176', '0.5566', '-0.34', '0.59', '-0.05695', '0.2028', '-0.2644', '-0.2219', '-0.11035', '0.0677', '-1.172', '0.5845', '-0.03067', '0.2367', '-0.1643', '0.539', '0.0394', '-0.33', '0.0773', '0.2039', '0.0376', '-0.05435', '0.07043', '0.2341', '0.02669', '-0.3125', '0.259', '-0.177', '0.3013', '-0.394', '-0.2585', '-0.671', '0.546', '0.146', '-0.1855', '-0.1799', '0.583', '-0.2115', '0.3086', '-0.626', '0.554', '0.5396', '0.3848', '0.09186', '-0.4507', '0.3755', '0.551', '0.2375', '0.334', '-0.0826', '0.271', '-0.2583', '-0.2542', '-0.183', '0.1198', '0.5083', '0.11163', '0.1461', '0.0592', '0.744', '-0.105', '-0.0825', '-0.224', '-0.2798', '0.5015', '0.6265', '0.11273', '-0.586', '-0.4275', '-0.55', '0.0208']",C3390,0000712,D020521,,,,0001297
mondo:0005099,subarachnoid hemorrhage,"['subarachnoid hemorrhage (disease)', 'subarachnoid hemorrhage', 'subarachnoid haemorrhage (disease)']",,,,C0038525,,,0000713,D013345,430,,,0002138
mondo:0005100,systemic sclerosis,"['systemic Scleroderma', 'Scleroderma syndrome', 'Scleroderma, diffuse', 'PSS (progressive systemic sclerosis)', 'Scleroderma', 'progressive systemic sclerosis', 'systemic scleroderma', 'SSc', 'Scleroderma, systemic', 'diffuse sclerosis', 'Scleroderma (& [systemic sclerosis])', 'diffuse Scleroderma', 'SSc, diffuse sclerosis', 'systemic sclerosis']",418,,90291,CN206012,,C72070,0000717,D012595,710.1,,10042953,
mondo:0005101,ulcerative colitis,"['colitis ulcerative', 'ulcerative proctosigmoiditis', 'ulcerative colitis', 'left-sided ulcerative colitis', 'ulcerative colitis (disease)']",8577,,771,C0009324,"['-0.2803', '-0.1422', '-0.2487', '0.3286', '-0.2559', '-0.5483', '0.386', '0.4143', '-0.2983', '0.474', '0.383', '0.1685', '-0.407', '0.521', '-0.2673', '-0.296', '-0.0586', '0.2908', '0.1499', '-0.861', '0.3135', '-0.03326', '0.055', '-0.4246', '0.2233', '-0.1798', '0.3225', '0.6846', '0.1646', '0.03647', '0.728', '-0.7705', '-0.1088', '0.01075', '0.003405', '-0.06104', '-1.351', '-0.0433', '0.461', '0.0901', '0.0701', '-0.0781', '0.201', '-0.02347', '0.429', '0.1665', '-0.0476', '-0.2795', '0.0854', '0.656', '0.003765', '-0.4202', '0.01823', '-0.348', '-0.1655', '-0.1477', '-0.3633', '0.4478', '-0.4807', '-0.718', '0.1181', '0.3345', '0.5083', '-0.4023', '0.1964', '0.6606', '0.7817', '0.1975', '-0.101', '0.7847', '0.5015', '0.3237', '0.01808', '-0.261', '-0.2507', '0.6904', '0.36', '0.9917', '0.757', '-0.7593', '-0.4324', '-0.152', '0.1155', '-0.2018', '0.1918', '-0.2153', '0.224', '-0.04385', '0.3657', '-0.4849', '-0.10126', '-0.00375', '0.275', '0.2642', '1.19', '0.4727', '-0.3672', '-0.6216', '-0.498', '-0.2113']",C2952,0000729,D003093,556.9,,,0100279
mondo:0005102,undifferentiated (embryonal) sarcoma,"['embryonal sarcoma', 'sarcoma, undifferentiated, malignant', 'embryonal sarcoma (undifferentiated sarcoma)', 'undifferentiated sarcoma', 'undifferentiated (embryonal) sarcoma', 'UES', 'embryonal sarcoma, undifferentiated']",,,,C0855073,,C27096,0000730,,,,,
mondo:0005103,well-differentiated liposarcoma,"['well-differentiated liposarcoma', 'atypical lipomatous tumor', 'well differentiated liposarcoma of deep soft tissue', 'well differentiated liposarcoma', 'atypical lipomatous tumour', 'WDLS', 'ALT', 'atypical lipoma']",,,99971,C1370889,,C4250,0000736,,,,,
mondo:0005104,aJCC grade 1 sarcoma,"['well differentiated sarcoma', 'aJCC grade I sarcoma', 'aJCC grade 1 sarcoma', 'aJCC G1 sarcoma']",,,,C1332066,,C9419,0000737,,,,,
mondo:0005105,melanoma,"['melanoma (disease)', 'melanoma, malignant', 'malignant melanoma', 'Naevocarcinoma', 'melanoma']",1909,,411533,CN971653,"['0.4487', '0.02899', '-0.816', '0.3113', '0.5586', '0.2283', '-0.1078', '0.0966', '-0.3997', '0.09406', '0.9653', '0.2008', '-0.735', '0.564', '-0.6816', '-0.211', '0.2961', '-0.3728', '-0.08624', '-0.05002', '-0.04517', '0.2607', '-0.1969', '-0.3784', '0.2255', '-0.7134', '-0.527', '-0.1724', '0.1288', '0.1162', '0.6074', '-0.7144', '0.2094', '-0.1545', '0.352', '0.6885', '-0.4324', '0.00932', '0.06186', '-0.5073', '0.3098', '-0.902', '0.09515', '-0.1223', '-0.04327', '-0.502', '-0.06024', '-0.4175', '-0.1692', '-0.416', '0.1427', '-0.1962', '0.01135', '-0.3308', '-0.7817', '-0.3691', '-0.183', '-0.00823', '-0.93', '-0.505', '-0.07684', '-0.094', '-0.8687', '0.681', '0.09045', '1.411', '0.4458', '0.6323', '0.1522', '1.051', '0.221', '0.6475', '0.2413', '-0.1157', '0.2435', '0.346', '-0.9414', '0.4536', '-0.1077', '-0.2878', '0.0511', '-0.0986', '0.2465', '-0.1846', '-0.1042', '-0.845', '0.07965', '0.0811', '1.087', '-0.05087', '0.8384', '0.02092', '-0.3096', '0.536', '0.6714', '0.562', '-0.4258', '-0.8525', '-0.975', '0.6787']",C3224,0000756,D008545,,,,0002861
mondo:0005106,lipoma,"['benign tumor of adipose tissue', 'lipomatous tumor', 'tumour of adipose tissue', 'multiple lipomatosis', 'lipoma, benign', 'lipomatous tumour', 'benign tumour of adipose tissue', 'lipoma', 'lipomatous neoplasm (morphologic abnormality)', 'benign lipomatous tumour', 'lipomatous neoplasm', 'lipomatosis, familial multiple']",3315,,,C0206631,,C3192,0000759,D008067,214.9,,,
mondo:0005108,viral infectious disease,"['viral infection', 'viral disorder', 'infection, viral', 'virus infection', 'viral disease', 'Viruses infection', 'Viruses caused disease or disorder', 'infections, Viruses']",934,,,,,C3439,0000763,D014777,079.99,,,
mondo:0005109,HIV infectious disease,"['Human immunodeficiency virus caused disease or disorder', 'human immunodeficiency virus infectious disease', 'HIV infection']",526,,,C0019693,,C3108,0000764,D015658,042-042.99,B20-B20,,
mondo:0005110,idiopathic cardiomyopathy,,,,,,,C53654,0000767,,,,,
mondo:0005111,Epstein-Barr virus infection,"['Human Herpes Virus 4 infections', 'Human gammaherpesvirus 4 caused disease or disorder', 'Virus infections, Epstein-Barr', 'infections, EBV', 'Epstein Barr Virus infections', 'Epstein-Barr Virus infection', 'infections, Epstein-Barr Virus', 'Herpesvirus 4 infections, Human', 'Human Herpesvirus 4 infections', 'EBV infections', 'EBV infection']",,,,C0149678,,C38759,0000769,D020031,,,,
mondo:0005112,malignant pleural mesothelioma,"['malignant mesothelioma of pleura', 'pleural malignant mesothelioma', 'pleura mesothelioma', 'malignant pleural mesothelioma', 'pleural diffuse malignant mesothelioma', 'malignant mesothelioma of the pleura']",7474,,,C0812413,,C7376,0000770,,,,,
mondo:0005113,bacterial infectious disease,"['infection, bacterial', 'bacterial infection', 'bacterial disorder', 'bacterial disease', 'Bacteria caused disease or disorder', 'infections, bacterial', 'bacterial infectious disease']",104,,,C0004623,,C2890,0000771,D001424,041.9,,,
mondo:0005114,pneumococcal infection,"['infection, pneumococcal', 'infections, pneumococcal', 'pneumoniae infection, Streptococcus', 'Streptococcus pneumoniae infections', 'Streptococcus pneumoniae infection', 'Streptococcus pneumoniae caused disease or disorder', 'pneumococcal infection', 'pneumoniae infections, Streptococcus', 'infections, Streptococcus pneumoniae', 'infection, Streptococcus pneumoniae']",,,,C0032269,,,0000772,D011008,041.2,,,
mondo:0005115,temporal lobe epilepsy,"['epilepsy of temporal lobe', 'epilepsy, temporal lobe', 'temporal lobe epilepsy', 'epilepsy, familial temporal lobe']",3328,,,C1842564,"['0.9385', '0.2346', '-0.2245', '-0.0738', '-0.53', '-0.3052', '0.8193', '0.00804', '-0.5938', '-0.392', '0.04', '-0.3499', '-0.3489', '0.1968', '-0.06506', '0.11316', '-0.2717', '-0.5547', '-0.3281', '-0.561', '-0.2974', '0.8203', '0.3545', '-0.6074', '-0.1921', '-0.1385', '-0.1131', '0.02023', '-0.4685', '0.443', '0.2037', '-0.6426', '0.3608', '0.0635', '0.884', '0.4353', '-0.01548', '0.06186', '-0.04514', '-0.6196', '-0.1993', '-0.212', '0.164', '-0.4785', '-0.5977', '-0.599', '-0.3257', '0.291', '0.65', '0.7676', '-0.002874', '0.2245', '0.006046', '-0.435', '0.02007', '-0.1968', '-0.1385', '0.054', '-0.1913', '0.4446', '-0.781', '0.505', '0.6597', '-0.2263', '-0.266', '1.646', '0.2443', '-0.0673', '-0.874', '0.92', '1.068', '1.178', '0.04947', '-0.3013', '0.1428', '0.72', '0.856', '0.2498', '-0.4111', '-0.05496', '-0.003227', '0.8135', '0.4575', '0.498', '0.4424', '0.1747', '0.2632', '0.7197', '0.683', '0.2988', '-0.0591', '0.00866', '-0.04288', '0.006912', '0.1875', '0.2156', '0.4248', '-0.6787', '0.1765', '0.3135']",C177244,0000773,D004833,,,,
mondo:0005116,Whipple disease,"['Whipple disease', 'intestinal lipophagic granulomatosis', 'intestinal lipodystrophy', 'Tropheryma whippelii infection', 'Tropheryma whipplei caused disease or disorder', 'secondary non-tropical sprue', 'Whipple^s disease']",8476,,3452,CN204440,,C85228,0000775,D008061,040.2,K90.81,10047931,
mondo:0005117,Aeromonas hydrophila infectious disease,['Aeromonas hydrophila caused disease or disorder'],,,,,,,0000776,,,,,
mondo:0005118,human granulocytic ehrlichiosis,"['human ehrlichial infection, human granulocytic type', 'human granulocytic anaplasmosis', 'HGE']",0050025,,,,,,0000777,,082.49,,,
mondo:0005119,anthrax infection,"['Bacillus anthracis caused disease or disorder', 'anthrax disease', 'anthrax']",7427,,,C0003175,,C84565,0000778,D000881,022.9,,,
mondo:0005120,Drosophila C virus infection,['Drosophila C virus caused disease or disorder'],,,,,,,0000779,,,,,
mondo:0005121,Enterococcus faecalis infection,['Enterococcus faecalis caused disease or disorder'],,,,,,,0000780,,,,,
mondo:0005122,Pectobacterium carotovorum infection,['Pectobacterium caused disease or disorder'],,,,,,,0000781,,,,,
mondo:0005124,leprosy,"['Hansen disease', 'Mycobacterium leprae caused disease or disorder', 'Hansen^s disease']",1024,,548,C0023343,,C84824,0001054,D007918,030.9,A30,10024229,
mondo:0005125,borderline leprosy,"['borderline or dimorphous leprosy', 'Midborderline leprosy', 'borderline leprosy [group B]']",1023,,,C3251797,,,0001055,D015439,030.3,A30.3,,
mondo:0005126,tuberculoid leprosy,"['smooth leprosy', 'tuberculoid leprosy [type T]', 'type T leprosy']",1025,,,C0023351,,,0001056,D015441,030.1,A30.1,,
mondo:0005127,lepromatous leprosy,"['type L leprosy', 'lepromatous leprosy [type L]']",10887,,,C0023348,,,0001057,D015440,030.0,A30.5,,
mondo:0005129,cataract,"['cataract', 'opacity of the lens', 'cataract (disease)']",83,,,,"['-0.1854', '0.1262', '-0.1425', '0.0792', '0.0965', '-0.2036', '0.1028', '0.2598', '-0.228', '-0.05383', '-0.0981', '-0.281', '-0.1737', '0.3008', '-0.1224', '-0.302', '0.1647', '-0.2302', '0.1271', '-0.3752', '-0.3452', '-0.0737', '0.03876', '-0.006714', '0.05856', '0.05936', '-0.11414', '0.292', '-0.1164', '0.2444', '0.3313', '-0.277', '0.1876', '0.2988', '0.05957', '0.0856', '0.1661', '-0.08997', '-0.0682', '-0.11914', '0.3489', '-0.06274', '0.04483', '0.1691', '-0.02441', '0.148', '-0.04977', '-0.07355', '-0.04395', '0.2446', '0.2578', '-0.02998', '0.1914', '0.0385', '-0.000243', '-0.1824', '0.5957', '-0.0752', '-0.2786', '0.0384', '0.1066', '-0.1354', '0.04834', '0.326', '-0.1191', '-0.01965', '0.427', '0.3433', '0.107', '0.1758', '-0.0689', '0.0789', '0.2399', '-0.1345', '0.2216', '-0.002693', '0.04202', '-0.05743', '-0.1193', '-0.1272', '-0.0712', '-0.1027', '-0.04697', '0.3538', '-0.0257', '-0.101', '-0.013794', '-0.05463', '0.3022', '-0.05865', '0.1384', '0.405', '-0.1531', '-0.013306', '0.3992', '-0.04706', '0.144', '-0.321', '0.02307', '0.0947']",C26713,0001059,D002386,366.9,,,0000518
mondo:0005130,celiac disease,"['non tropical sprue', 'celiac sprue', 'coeliac sprue', 'idiopathic steatorrhea', 'gluten intolerance', 'celiac disease', 'gluten-induced enteropathy']",10608,,555,C0007570,"['-0.2186', '0.349', '0.2798', '0.1611', '0.3372', '-0.1654', '-0.4678', '0.04648', '-0.01484', '-0.005398', '0.4312', '-0.08887', '-0.4875', '0.1998', '0.089', '0.4385', '0.1196', '0.1187', '-0.8228', '-0.699', '0.1641', '-0.5024', '-0.2351', '-0.2844', '-0.008', '-0.572', '-0.4624', '0.227', '0.1366', '-0.1231', '0.1676', '-0.4265', '0.1605', '-0.0851', '0.2263', '0.1909', '-0.46', '0.1431', '0.12195', '0.4238', '-0.425', '-0.2275', '0.4285', '-0.0713', '0.03815', '-0.8447', '0.1409', '-0.11505', '0.2344', '0.377', '-0.4055', '0.003124', '0.12036', '-0.04044', '-0.0453', '-0.00789', '-0.8047', '0.02567', '-0.4087', '-0.4111', '0.3462', '-0.1815', '0.05548', '-0.6035', '0.5166', '0.3352', '0.6406', '0.4678', '0.352', '0.6743', '-0.0512', '0.3198', '-0.217', '-1.001', '-0.09625', '-0.1442', '-0.0857', '0.635', '0.2263', '0.4065', '-0.18', '-0.1515', '-0.3872', '-0.06476', '0.1824', '-0.2189', '-0.01886', '-0.4338', '1.419', '0.2471', '-0.3452', '0.054', '-0.3035', '0.1342', '0.6436', '0.717', '-0.062', '-0.33', '-0.0376', '0.372']",C26714,0001060,D002446,579.0,K90.0,,
mondo:0005131,cervical carcinoma,"['carcinoma of the cervix', 'carcinoma of uterine cervix', 'uterine cervix carcinoma', 'cancer of uterine cervix', 'carcinoma of the uterine cervix', 'cervix uteri carcinoma', 'carcinoma of cervix', 'cervix cancer', 'cervix carcinoma', 'carcinoma of the cervix uteri', 'cancer of the uterine cervix', 'cancer of cervix', 'cervical cancer, NOS', 'uterine cervix cancer', 'carcinoma of cervix uteri', 'cervical cancer', 'cancer of the cervix', 'cervical carcinoma', 'carcinoma cervix uteri']",2893,,,C0302592,"['0.005848', '0.1338', '-0.1246', '-0.056', '0.09796', '-0.2634', '0.01294', '0.04163', '-0.004402', '0.1021', '-0.0869', '-0.163', '-0.2491', '0.10077', '-0.3748', '-0.2964', '0.0649', '-0.2708', '0.1885', '-0.315', '-0.1259', '-0.1034', '0.348', '-0.291', '0.3462', '-0.0216', '0.1213', '0.00861', '-0.1292', '-0.257', '0.3818', '-0.03247', '0.1123', '-0.05777', '0.2627', '-0.04874', '-0.2429', '-0.1385', '-0.0862', '-0.2498', '-0.01686', '-0.292', '0.1332', '-0.2037', '-0.04462', '-0.1649', '-0.177', '0.010345', '-0.02406', '-0.0802', '0.155', '-0.0899', '0.05396', '0.1298', '-0.283', '-0.12274', '0.3032', '0.12463', '-0.4294', '0.00879', '0.1892', '0.0299', '-0.1661', '0.168', '0.03146', '0.173', '0.424', '0.2747', '-0.1853', '0.414', '-0.05142', '-0.0301', '0.0717', '-0.03455', '0.05746', '-0.1087', '-0.01384', '-0.09235', '-0.09766', '-0.2544', '-0.3845', '0.2954', '-0.1382', '0.0637', '-0.3157', '-0.2878', '0.1245', '0.1115', '0.3416', '-0.3242', '-0.11334', '0.2944', '0.1466', '-0.006126', '0.427', '-0.11633', '0.2266', '-0.245', '-0.1735', '-0.01312']",C9039,0001061,,,,,
mondo:0005132,cytomegalovirus infection,"['HCMV infection', 'CMV infection', 'Cytomegaloviral infection']",,,,C0010823,,C53649,0001062,D003586,078.5,,,
mondo:0005133,endometriosis,"['endometriosis', 'endometriosis (disease)']",289,,,,,C3014,0001065,D004715,617.9,N80,,0030127
mondo:0005134,experimental autoimmune encephalomyelitis,,,,,,,,0001066,D004681,,,,
mondo:0005135,parasitic infectious disease,"['ectoparasitic disease', 'parasitic disease', 'parasitic infectious disease', 'disease, parasitic', 'parasitemia', 'parasitic infection', 'diseases, parasitic']",1398,,,,,C27864,0001067,D010272,376.13,,,
mondo:0005136,malaria,,12365,,673,C0024530,,C34797,0001068,D008288,084.6,B53.0,10025487,
mondo:0005137,nutritional disorder,"['nutrition disease', 'nutritional disorder']",374,,,C3714509,,C26836,0001069,D009748,783.9,,,
mondo:0005138,lung carcinoma,"['carcinoma of the lung', 'carcinoma of lung', 'lung carcinoma', 'lung cancer, NOS', 'cancer of lung', 'cancer of the lung', 'lung cancer']",3905,,,C0684249,"['-0.07654', '0.1293', '-0.0593', '0.10767', '0.02298', '-0.1614', '0.0907', '0.04703', '-0.06616', '-0.11774', '0.00928', '-0.04068', '-0.09393', '0.1244', '-0.2139', '-0.2202', '-0.04544', '-0.1151', '0.0853', '-0.294', '-0.053', '-0.1439', '0.2021', '-0.2427', '0.1581', '-0.1598', '-0.01118', '0.0797', '-0.09247', '-0.1755', '0.2188', '0.02461', '0.1804', '-0.07117', '0.02435', '-0.0541', '-0.1357', '0.02307', '0.06555', '-0.03854', '0.00785', '-0.2125', '0.03802', '-0.0692', '-0.0493', '-0.02481', '-0.0768', '-0.02261', '0.1459', '0.02267', '0.05774', '0.0004609', '0.0821', '0.1287', '-0.1785', '-0.05252', '0.1498', '0.01021', '-0.2426', '-0.06445', '0.1871', '0.0878', '0.0005937', '0.0372', '0.04446', '0.044', '0.3232', '0.2612', '-0.2068', '0.1835', '-0.01395', '0.04877', '0.1395', '0.01441', '0.03778', '-0.008644', '-0.04346', '-0.0387', '-0.0836', '-0.2433', '-0.2407', '0.03708', '-0.0789', '0.03653', '-0.2452', '-0.097', '0.11865', '0.095', '0.2039', '-0.0767', '0.05414', '0.2725', '-0.02454', '-0.02176', '0.3289', '0.087', '0.0785', '-0.2072', '-0.0945', '0.08826']",C4878,0001071,,,,,
mondo:0005139,morbid obesity,['severe obesity'],11981,,,C0028756,,,0001074,D009767,278.01,,,
mondo:0005140,ovarian carcinoma,"['ovary carcinoma', 'carcinoma of the ovary', 'carcinoma of ovary', 'ovarian epithelial cancer', 'ovarian carcinoma', 'ovarian cancer', 'epithelial ovarian cancer']",4001,,,,"['0.0755', '0.2222', '-0.1902', '0.11444', '0.27', '-0.2094', '0.4963', '0.194', '-0.2258', '-0.053', '-0.1932', '0.1747', '-0.5493', '0.2756', '-0.2512', '-0.4585', '-0.0394', '-0.1836', '0.011536', '-0.3625', '-0.3376', '-0.406', '0.4062', '-0.637', '0.1509', '-0.245', '0.1869', '0.1086', '-0.1938', '-0.1316', '0.8174', '-0.0669', '0.2605', '-0.2612', '0.1924', '0.09076', '-0.2927', '0.014946', '0.0698', '0.433', '0.06854', '-0.1719', '0.2095', '-0.03372', '0.04333', '0.07684', '-0.2114', '-0.2695', '0.0459', '0.1744', '0.3977', '-0.2454', '-0.3398', '0.01695', '-0.428', '-0.09485', '0.1353', '0.03986', '-0.2181', '-0.199', '0.3567', '0.1931', '-0.0483', '0.2128', '0.1218', '0.125', '0.273', '0.2224', '-0.014145', '0.3228', '0.0629', '-0.1287', '-0.03714', '-0.1292', '-0.00918', '0.1013', '-0.09937', '-0.1161', '-0.0924', '-0.6714', '-0.448', '-0.1729', '-0.142', '0.0478', '-0.4229', '-0.3777', '0.3787', '-0.2411', '0.09406', '-0.497', '-0.1353', '0.1628', '-0.259', '-0.05267', '0.8057', '-0.2284', '0.08716', '-0.546', '0.11005', '-0.1624']",C4908,0001075,,,,,
mondo:0005141,Pseudomonas infection,['Pseudomonas caused disease or disorder'],,,,,,,0001076,D011552,041.7,,,
mondo:0005142,Pseudomonas aeruginosa CF5 infection,,,,,,,,0001077,,,,,
mondo:0005143,Pseudomonas aeruginosa PA14 infection,,,,,,,,0001078,,,,,
mondo:0005144,familial amyotrophic lateral sclerosis,['hereditary amyotrophic lateral sclerosis'],,,,,"['-0.1045', '0.1948', '0.03772', '-0.0338', '-0.001349', '-0.217', '0.06866', '-0.00524', '-0.252', '-0.1255', '0.2013', '0.02234', '0.02783', '-0.1407', '0.1582', '-0.2338', '-0.1102', '-0.1131', '0.05652', '-0.4033', '0.1444', '-0.1231', '0.0945', '-0.05783', '0.1802', '-0.013306', '0.05515', '0.0949', '-0.03403', '0.0673', '0.09735', '-0.04648', '0.1826', '-0.0853', '0.1636', '-0.0643', '-0.0546', '0.01997', '0.0413', '-0.3596', '0.191', '-0.1501', '0.0457', '-0.1875', '0.2039', '-0.1421', '0.0549', '0.0971', '0.2612', '0.0722', '0.03256', '0.05713', '-0.04407', '0.1177', '-0.1669', '-0.4294', '0.1385', '0.1116', '-0.4724', '0.0769', '0.2666', '0.062', '0.1455', '0.0944', '-0.09314', '0.1471', '0.3645', '0.03256', '-0.2355', '0.2786', '-0.2117', '-0.08496', '0.1311', '-0.0973', '-0.05087', '0.2246', '-0.06866', '0.2043', '-0.2998', '-0.275', '-0.0266', '0.1667', '-0.0408', '0.2343', '-0.1187', '-0.144', '0.02658', '-0.0009017', '0.1316', '0.04266', '-0.00563', '0.06305', '0.0952', '0.03256', '0.3425', '0.1919', '0.315', '-0.1763', '-0.03174', '0.012024']",,0001356,,,,,
mondo:0005145,sporadic amyotrophic lateral sclerosis,,0080917,,,,"['-0.11835', '0.09204', '-0.03268', '0.02747', '-0.1469', '-0.4531', '0.1901', '0.0957', '-0.3938', '-0.07764', '0.1832', '0.00674', '-0.1935', '-0.1257', '0.3884', '-0.2186', '-0.108', '-0.10925', '0.0718', '-0.2198', '0.2085', '-0.1766', '0.06274', '-0.1597', '0.1593', '-0.0782', '-0.07587', '0.0339', '-0.002893', '0.01447', '0.153', '-0.1699', '0.1028', '-0.0683', '0.4807', '-0.0803', '-0.2198', '-0.0979', '0.1436', '-0.2869', '0.2034', '-0.2252', '-0.09186', '-0.3154', '0.3677', '-0.284', '0.0768', '0.2515', '-0.0847', '0.1454', '0.095', '0.10095', '0.06107', '0.0823', '-0.0731', '-0.322', '0.10864', '-0.0189', '-0.3577', '0.1685', '0.0361', '-0.103', '0.06537', '0.02052', '0.05048', '0.1958', '0.3318', '0.02994', '-0.3132', '0.517', '-0.0228', '-0.11', '-0.0693', '-0.3137', '-0.0726', '0.1202', '0.03357', '0.0767', '-0.1653', '-0.1137', '-0.1656', '0.08026', '-0.10614', '0.3071', '-0.07404', '-0.2313', '-0.05783', '0.01811', '0.1989', '0.1672', '0.05917', '-0.0815', '0.05496', '-0.0634', '0.5044', '0.1691', '0.292', '-0.11523', '0.0705', '-0.1617']",,0001357,,,,,
mondo:0005146,post-traumatic stress disorder,"['PTSD', 'combat neurosis', 'traumatic neurosis', 'post-traumatic stress disorder']",2055,,,,,C3389,0001358,D013313,309.81,,,
mondo:0005147,type 1 diabetes mellitus,"['juvenile diabetes', 'insulin dependent diabetes', 'immune mediated diabetes', 'type I diabetes mellitus', 'type 1 diabetes', 'type I diabetes', 'insulin-dependent diabetes mellitus', 'IDDM']",9744,222100,243377,,"['0.727', '-0.2484', '0.07477', '0.689', '-0.3716', '-0.804', '-0.2935', '0.9937', '0.07855', '-0.568', '0.083', '-0.4077', '0.3171', '0.2325', '-1.107', '-0.2776', '0.395', '0.1832', '0.0864', '-0.5825', '0.1647', '-0.10614', '0.0707', '-0.0558', '-0.8706', '-0.4058', '0.10236', '0.01967', '0.4065', '-0.4626', '0.949', '-0.468', '0.07684', '-0.2062', '-0.2065', '0.689', '-0.639', '0.449', '0.1288', '-0.159', '0.027', '0.4207', '0.2598', '0.4424', '-0.3506', '-0.3215', '0.3362', '-0.2034', '-0.01029', '0.2996', '0.2595', '-0.5127', '0.668', '-0.892', '0.01776', '0.4856', '0.0791', '-0.8477', '-1.087', '0.4448', '-0.3933', '0.4795', '-0.1953', '0.2035', '-0.06757', '0.8887', '-0.4138', '0.7275', '-0.874', '0.2834', '0.4712', '0.3157', '0.0992', '-0.3918', '0.767', '0.434', '-0.5845', '1.045', '-0.2583', '-0.2683', '0.167', '0.1942', '-0.0975', '-0.5063', '0.2607', '0.2186', '0.04688', '0.489', '0.802', '0.06073', '0.6206', '0.408', '-0.0902', '-0.3591', '1.323', '0.2583', '-0.3008', '-0.1902', '-0.376', '0.156']",C2986,0001359,D003922,,,,
mondo:0005148,type 2 diabetes mellitus,"['non-insulin-dependent diabetes mellitus', 'diabetes mellitus, type 2, protection against', 'diabetes mellitus, type II, susceptibility to', 'maturity-onset diabetes', 'insulin resistance, susceptibility to', 'noninsulin-dependent diabetes mellitus', 'type 2 diabetes mellitus', 'diabetes mellitus, noninsulin-dependent, association with', 'diabetes, type 2', 'type II diabetes', 'type II diabetes mellitus', 'non-insulin dependent diabetes mellitus', 'diabetes mellitus, type II', 'diabetes mellitus, noninsulin-dependent', 'insulin resistance, severe, digenic', 'diabetes mellitus, type 2', 'hypertension, insulin resistance-related, susceptibility to', 'diabetes mellitus, noninsulin-dependent, 2', 'type 2 diabetes', 'noninsulin dependent diabetes', 'NIDDM', 'adult onset diabetes', 'adult-onset diabetes', 'type 2 diabetes mellitus, susceptibility to', 'diabetes mellitus, non-insulin-dependent, susceptibility to', 'T2DM - type 2 diabetes mellitus', 'diabetes mellitus, noninsulin-dependent, susceptibility to', 'diabetes mellitus, type 2, susceptibility to', 'type 2 diabetes mellitus non-insulin dependent', 'non-insulin dependent diabetes', 'diabetes mellitus, noninsulin-dependent, late onset']",9352,125853,,CN244395,"['0.5244', '0.2932', '-0.02153', '0.694', '0.02736', '-0.2654', '-0.529', '0.609', '-0.33', '-0.3936', '0.01132', '-0.153', '-0.02608', '0.5884', '-0.2583', '0.08307', '-0.1813', '0.4324', '-0.2996', '-0.531', '-0.2754', '-0.3704', '-0.2429', '0.04736', '-0.4626', '-0.5537', '-0.05197', '0.0604', '0.713', '-0.3762', '0.784', '-0.108', '0.09985', '0.1952', '-0.316', '0.434', '-0.68', '0.793', '0.1497', '-0.528', '0.01816', '0.1995', '-0.1388', '0.2861', '-0.1373', '-0.08655', '0.4673', '0.04208', '0.1798', '0.11066', '-0.03482', '-0.1857', '0.798', '-0.0259', '0.1987', '0.1877', '0.2272', '-0.2238', '-0.4353', '-0.089', '-0.3887', '0.05844', '-0.02466', '0.011826', '-0.1494', '0.3608', '-0.1436', '0.2264', '-0.761', '0.1841', '0.6333', '0.3708', '0.2179', '-0.3652', '0.6226', '0.3079', '-0.4536', '1.003', '-0.0415', '-0.5073', '-0.2825', '-0.1538', '-0.29', '-0.4224', '-0.006897', '0.209', '-0.1159', '0.1292', '0.915', '0.2', '0.3567', '0.3591', '-0.3547', '0.1663', '0.762', '0.1777', '-0.2476', '-0.531', '-0.2094', '0.4583']",C26747,0001360,D003924,,,,
mondo:0005149,pulmonary hypertension,,6432,,,,"['0.2479', '-0.06024', '-0.1881', '0.3076', '0.01707', '-0.2793', '0.04025', '0.4768', '-0.5303', '-0.2551', '0.2461', '-0.01371', '0.2883', '0.546', '-0.1754', '-0.754', '-0.03004', '0.741', '-0.1979', '-0.4583', '0.02531', '-0.309', '-0.02383', '0.116', '0.0543', '-0.5107', '-0.03232', '-0.04065', '0.1826', '0.5474', '0.615', '-0.3445', '0.674', '0.082', '-0.04626', '0.07324', '-0.331', '0.2365', '0.523', '-0.576', '0.461', '0.009094', '0.08777', '-0.007313', '0.514', '0.1947', '0.1598', '0.188', '0.2019', '0.0463', '0.2291', '0.553', '0.521', '-0.1703', '-0.1175', '-0.1118', '-0.06195', '0.1537', '-0.4836', '-0.106', '-0.3647', '0.69', '-0.3508', '-0.1847', '-0.6333', '0.1504', '-0.3083', '0.1653', '-1.045', '0.59', '0.3052', '0.5317', '-0.04843', '-0.5522', '-0.01762', '0.383', '0.0688', '0.2477', '-0.3445', '0.03568', '-0.1664', '0.2219', '-0.04233', '0.0949', '0.4895', '-0.08453', '0.2769', '-0.09784', '0.844', '0.072', '-0.42', '-0.5264', '-0.4', '0.1945', '0.635', '0.329', '-0.4377', '-0.282', '-1.031', '0.006016']",,0001361,D006976,,,10037400,
mondo:0005150,age-related macular degeneration,"['age related Maculopathies', 'age-related macular degeneration', 'Senile macular degeneration', 'ARMD', 'age related maculopathy', 'macular degeneration, age-related', 'AMD', 'age related macular degeneration', 'Senile macular retinal degeneration']",10871,,279,C0242383,"['0.1088', '-0.1937', '0.02255', '0.5156', '-0.1677', '-0.0812', '0.05258', '0.5435', '-0.3538', '-0.8467', '0.2477', '-0.4612', '-0.2766', '0.4268', '-0.09766', '-0.761', '0.32', '0.2164', '-0.0971', '-0.296', '0.093', '-0.277', '-0.1433', '0.2961', '0.03943', '0.2666', '-0.05646', '-0.3552', '-0.2898', '0.03134', '0.5825', '-0.0473', '0.2502', '-0.2761', '0.355', '0.4382', '-0.1448', '-0.336', '0.04727', '-0.5737', '0.545', '-0.586', '0.1434', '-0.2092', '-0.2961', '0.0649', '0.0752', '-0.4783', '0.4158', '0.01895', '-0.03317', '-0.2717', '0.153', '-0.9863', '0.148', '-0.10706', '0.4778', '0.4348', '-0.6045', '-0.7495', '-0.5293', '-0.0856', '0.2109', '0.06134', '-0.1531', '0.6226', '0.1228', '0.7056', '0.0657', '1.139', '0.6', '0.077', '0.03552', '-0.0909', '0.05276', '0.523', '-0.442', '0.6836', '-0.371', '0.208', '0.3584', '-0.822', '-0.709', '0.82', '0.295', '-0.05975', '0.0959', '-0.4998', '0.863', '0.2024', '-0.348', '0.2087', '-0.1624', '0.639', '0.8267', '-0.0933', '-0.3293', '-0.124', '-0.502', '-0.2021']",C84391,0001365,,362.50,,,
mondo:0005151,endocrine system disorder,"['endocrine system disease or disorder', 'endocrine system disorder', 'endocrine disease', 'disease of endocrine system', 'thyroid or other glandular disorders', 'endocrine disorder', 'endocrine system disease', 'endocrinopathy', 'disorder of endocrine system']",28,,,C0014130,,C3009,0001379,D004700,259.9,,,
mondo:0005152,hypopituitarism,"['pituitary insufficiency', 'pituitary hypofunction', 'pituitary hormone deficiency']",9406,,95494,C0020635,"['-0.7036', '-0.1245', '-0.299', '-0.3225', '0.01587', '0.258', '0.3447', '-0.1055', '-0.383', '-0.3855', '0.253', '-0.0712', '-0.07465', '0.619', '-0.5435', '-0.2003', '-0.02383', '0.5977', '-0.733', '-0.516', '-0.0835', '-0.3362', '0.1444', '-0.435', '0.3135', '0.1412', '-0.4138', '-0.133', '-0.548', '0.2299', '0.332', '0.04242', '0.732', '0.0922', '-0.0874', '0.4314', '-0.3235', '0.1516', '-0.05124', '0.4153', '0.2742', '-0.10895', '-0.2041', '-0.4692', '0.4202', '-0.341', '0.1643', '-0.3665', '0.633', '0.521', '-0.03766', '0.3757', '-0.01192', '0.04694', '-0.04373', '0.536', '0.432', '0.03162', '-0.149', '-0.10187', '-0.1595', '0.4148', '-0.406', '-0.3704', '-0.3972', '0.775', '0.4746', '0.549', '-0.2937', '-0.1065', '-0.4968', '0.3667', '0.313', '-0.5737', '0.4229', '0.067', '-0.2903', '0.4927', '0.3442', '0.2786', '-0.08685', '0.3613', '-0.04044', '-0.3994', '0.05423', '0.04233', '0.4412', '-0.513', '1.008', '0.01657', '-0.0854', '0.4902', '0.04456', '-0.3418', '1.071', '0.2874', '-0.53', '-0.3816', '0.1326', '0.3296']",C62591,0001380,D007018,,E23.0,,
mondo:0005153,cervical adenocarcinoma,"['cervix uteri adenocarcinoma', 'adenocarcinoma of the cervix uteri', 'adenocarcinoma of the cervix', 'adenocarcinoma - cervix', 'cervical adenocarcinoma', 'adenocarcinoma of cervix', 'adenocarcinoma cervix uteri', 'adenocarcinoma of the uterine cervix', 'uterine cervix adenocarcinoma', 'adenocarcinoma of cervix uteri', 'adenocarcinoma of uterine cervix', 'cervix adenocarcinoma']",3702,,213772,,"['0.02855', '0.1793', '-0.03696', '-0.1349', '0.2454', '-0.1304', '0.1584', '0.01203', '-0.01953', '-0.1821', '-0.11127', '0.1111', '-0.2439', '0.00687', '-0.306', '-0.271', '0.1278', '-0.38', '-0.117', '-0.1681', '-0.1043', '-0.1685', '0.301', '-0.4045', '0.2313', '0.0587', '0.2896', '0.0487', '-0.1917', '-0.1299', '0.3738', '0.02225', '0.1802', '-0.3762', '0.2705', '0.006153', '-0.162', '-0.2177', '0.02043', '-0.3027', '0.1608', '-0.1091', '0.2993', '-0.305', '-0.1788', '-0.186', '-0.229', '-0.10474', '0.1375', '0.2659', '0.0594', '-0.085', '-0.1285', '0.04077', '-0.3184', '0.089', '0.376', '-0.1272', '-0.3098', '-0.03008', '0.3376', '0.2244', '-0.3652', '0.09', '-0.04254', '0.2421', '0.294', '0.1997', '-0.0333', '0.561', '-0.08484', '-0.00976', '-0.02824', '-0.0894', '0.2666', '-0.0637', '-0.1998', '-0.04547', '-0.205', '-0.2969', '-0.4385', '0.1676', '0.1095', '-0.0731', '-0.185', '-0.1975', '0.1329', '0.1287', '0.2195', '-0.4165', '-0.0749', '0.1456', '-0.1726', '0.0656', '0.512', '-0.1376', '0.317', '-0.3923', '-0.2042', '-0.4343']",C4029,0001416,,,C53.0,,
mondo:0005154,liver disorder,"['disease of liver', 'hepatic disease', 'disorder of liver', 'liver disease or disorder', 'liver and intrahepatic bile duct disorder', 'hepatic disorder', 'liver disease', 'liver disorder']",409,,,C0023895,,C3196,0001421,D008107,573.9,K70-K77,,
mondo:0005155,cirrhosis of liver,"['liver cirrhosis', 'cirrhosis of liver', 'cirrhosis']",5082,,,C0023890,"['-0.04654', '0.02269', '0.7217', '-0.2632', '-0.142', '-0.0827', '-0.11456', '-0.05023', '0.0676', '0.356', '0.5464', '-0.369', '-0.1244', '0.2043', '-0.6196', '-0.907', '-0.002121', '0.3032', '-0.07983', '-0.553', '-0.1929', '-0.2408', '0.392', '0.05975', '-0.1945', '-0.3833', '0.1779', '0.785', '-0.2522', '-0.4365', '0.6826', '-0.5396', '0.4014', '-0.04193', '0.1921', '-0.00612', '-0.582', '0.1874', '0.2338', '-0.4998', '-0.0439', '0.2455', '-0.02237', '0.655', '0.01656', '0.146', '0.3057', '-0.4663', '0.7603', '-0.2812', '-0.3105', '0.1713', '0.18', '-0.06683', '-0.728', '-0.2102', '-0.05054', '-0.1577', '-1.002', '-0.387', '0.3135', '0.0625', '0.0906', '-0.563', '-0.2842', '0.0505', '-0.01351', '0.4036', '-0.63', '0.519', '-0.16', '0.44', '0.04602', '-0.4006', '0.2698', '0.10516', '0.3833', '0.657', '0.473', '0.0598', '-0.05313', '-0.3118', '-0.3801', '-0.2388', '0.1714', '0.03436', '0.05423', '-0.418', '0.836', '-0.4841', '0.5293', '0.872', '-0.522', '0.5146', '0.507', '0.3538', '-0.2651', '-0.2886', '0.269', '-0.0919']",C2951,0001422,D008103,571.5,,,
mondo:0005156,encephalomyelitis,"['central nervous system inflammation', 'encephalitis &/or myelitis', 'encephalitis and/or myelitis']",640,,,C0014070,,C34580,0001423,D004679,323.9,,,
mondo:0005157,lymphoid neoplasm,"['lymphocytic and plasmacytic neoplasm', 'lymphoid neoplasm', 'lymphocytic and plasma cell neoplasm', 'lymphoid and plasmacytic tumor', 'lymphocytic neoplasm', 'lymphoid and plasma cell tumor', 'lymphoid tumor', 'lymphoid and plasma cell tumour', 'lymphoid and plasmacytic neoplasm', 'lymphocytic and plasma cell tumour', 'lymphocytic and plasma cell tumor', 'lymphocytic tumour', 'lymphocytic tumor', 'lymphoid and plasmacytic tumour', 'lymphoid tumour']",,,,C0598798,,C7065,0001642,,200.7,,,
mondo:0005159,prostate carcinoma,"['prostate gland carcinoma', 'carcinoma of the prostate', 'prostate carcinoma', 'cancer of the prostate', 'prostate cancer, NOS', 'prostate cancer', 'cancer of prostate', 'carcinoma of prostate gland', 'carcinoma of prostate']",10286,,,C0600139,"['-0.1685', '0.126', '0.02238', '0.09357', '0.0396', '-0.0741', '0.06946', '0.09106', '-0.0515', '-0.1495', '-0.04062', '-0.01595', '-0.0921', '0.1262', '-0.2441', '-0.1803', '0.01019', '-0.11523', '0.0729', '-0.2544', '-0.05643', '-0.1216', '0.0891', '-0.1788', '0.202', '-0.09766', '0.0707', '0.01207', '-0.0524', '-0.2413', '0.2166', '-0.02348', '0.1266', '-0.11096', '0.03574', '-0.0425', '-0.07007', '0.083', '0.06', '-0.093', '0.02446', '-0.2035', '0.01746', '-0.2028', '-0.06555', '-0.1173', '0.01611', '-0.05325', '0.1255', '0.01848', '0.0198', '0.05655', '0.0562', '0.1178', '-0.2003', '0.0301', '0.176', '-0.001835', '-0.2747', '-0.03616', '0.2617', '0.1675', '-0.06995', '0.03104', '0.006508', '0.1587', '0.3054', '0.2898', '-0.1606', '0.1886', '0.001772', '0.02153', '0.11835', '-0.05753', '0.04642', '-0.010376', '-0.02446', '0.0628', '-0.1116', '-0.182', '-0.252', '0.1271', '-0.0996', '-0.04822', '-0.1969', '-0.1339', '0.0872', '0.0395', '0.1958', '-0.1514', '0.001175', '0.2114', '0.0343', '-0.03857', '0.4165', '-0.02988', '0.06204', '-0.1708', '-0.1284', '0.1349']",C4863,0001663,,,,,
mondo:0005160,aortic aneurysm,"['aortic aneurysm (disease)', 'thoracoabdominal aortic aneurysm, ruptured', 'abdominal aortic aneurysm, ruptured', 'aortic aneurysm', 'thoracic aortic aneurysm which HAS ruptured', 'ruptured thoracic aortic aneurysm', 'aortic aneurysm of unspecified site, ruptured', 'ruptured abdominal aortic aneurysm', 'thoracic aortic aneurysm, ruptured', 'ruptured thoracoabdominal aortic aneurysm', 'ruptured aortic aneurysm', 'ruptured thoracic aneurysm']",3627,,,C1305122,,,0001666,D001014,441.6,,,0004942
mondo:0005161,human papilloma virus infection,"['Human papilloma Virus infection', 'Human papillomavirus caused disease or disorder', 'Human Papillomavirus infection']",11166,,,C0343641,,C27851,0001668,,079.4,,,
mondo:0005163,simian immunodeficiency virus infection,['Simian immunodeficiency virus caused disease or disorder'],,,,,,,0001675,,,,,
mondo:0005164,fibrosarcoma,"['fibrocytic tumour', 'fibrosarcoma (disease)', 'fibrosarcoma, malignant', 'fibrosarcoma - not infantile', 'fibrosarcoma of soft tissue', 'fibrosarcoma', 'fibrosarcoma (excluding infantile fibrosarcoma)', 'malignant fibromatous neoplasm', 'fibrocytic tumor', 'fibrous tissue neoplasm']",3355,,2030,C0016057,,C3043,0002087,D005354,171.9,,10016632,0100244
mondo:0005165,benign neoplasm,"['benign unclassifiable tumour', 'organ system benign neoplasm', 'neoplasm (disease), benign', 'benign unclassifiable tumor', 'neoplasm, benign', 'cell type benign neoplasm', 'benign neoplasm', 'benign tumor', 'benign tumour']",0060085,,,,,C3677,0002422,,229.9,D10-D36,,
mondo:0005166,osteoma,"['osteoma', 'osteoma (disease)', 'osteoma, benign']",,,,C0029440,,C3296,0002423,D010016,,,,0100246
mondo:0005167,fibroma,"['fibroma, benign', 'fibroma']",0050871,,,,,C3041,0002424,D005350,215.9,,,
mondo:0005168,neoplasm of immature B and T cells,,,,,,,,0002425,,,,,
mondo:0005169,neoplasm of mature T-cells or NK-cells,"['mature T-cell neoplasm', 'mature T-cell and NK-cell neoplasm']",,,,C1334640,,C27909,0002426,,,,,
mondo:0005170,myeloid neoplasm,"['myeloid neoplasm', 'myeloid malignancy', 'myeloid tumor', 'myeloid tumour']",0070004,,,C2939461,,C9290,0002427,,,,,
mondo:0005172,skeletal system disorder,"['disorder of skeletal system', 'skeletal system disease or disorder', 'skeletal system disease', 'disease of skeletal system']",,,,C0263661,,,0002461,,,,,
mondo:0005173,actinic keratosis,"['actinic (solar) keratosis', 'solar keratosis', 'Senile hyperkeratosis', 'SK - solar keratosis', 'actinic keratosis', 'senile keratosis', 'Senile keratosis', 'actinic keratosis (disease)']",8866,,,C0022602,,C3148,0002496,D055623,702.19,L57.0,,0025127
mondo:0005174,acute hypotension,"['hypotension (disease), acute']",,,,,,,0002497,,,,,
mondo:0005175,aggressive insulitis,,,,,,,,0002498,,,,,
mondo:0005176,benign insulitis,,,,,,,,0002502,,,,,
mondo:0005177,serous cystadenoma,"['serous cystadenoma', 'serous cystoma']",,,,,,C3783,0002504,,,,,
mondo:0005178,osteoarthritis,"['degenerative arthritis', 'hypertrophic arthritis', 'osteoarthrosis', 'degenerative joint disease', 'osteoarthrosis and allied disorder']",8398,,,C0029408,"['-0.3184', '0.3635', '0.1175', '0.2343', '0.09204', '-0.7256', '-0.1179', '0.4463', '-0.4717', '-0.3232', '0.238', '0.921', '0.03047', '0.592', '0.1847', '-0.09534', '0.2168', '0.2039', '-0.6675', '-0.808', '0.6123', '0.1356', '0.2002', '-0.2288', '-0.6387', '0.349', '0.0807', '-0.3955', '0.1415', '-0.003319', '0.0506', '-0.507', '0.346', '0.5474', '0.5474', '-0.08984', '0.1387', '-0.553', '0.3313', '-0.942', '0.719', '0.2134', '-0.7827', '0.6636', '0.0939', '0.07446', '0.2302', '-0.1997', '0.547', '-0.171', '-0.0003765', '0.098', '0.786', '0.349', '0.795', '-0.329', '0.2573', '0.0623', '-0.3872', '-0.1605', '0.6733', '0.1788', '-0.8574', '-0.5327', '-0.743', '0.0781', '0.2903', '0.656', '0.04614', '0.7314', '0.1792', '0.1008', '-0.045', '-0.7407', '0.255', '0.1917', '-0.0911', '1.709', '0.013664', '-0.454', '-0.5986', '-0.2163', '0.167', '0.3936', '0.603', '0.3164', '-0.26', '0.4639', '0.5376', '-0.11975', '0.2019', '0.4836', '-0.2146', '0.010635', '-0.1648', '0.394', '-0.1041', '-0.4316', '-0.3435', '-0.2952']",C3293,0002506,D010003,715.3,M19,,0002758
mondo:0005179,ovarian adenoma benign,,,,,,,,0002507,,,,,
mondo:0005180,Parkinson disease,"['paralysis agitans', 'Parkinson^s disease']",14330,,319705,C0030567,"['-0.276', '0.4158', '-0.1626', '0.1449', '-0.2338', '-0.4253', '0.2263', '0.4153', '-0.3198', '-0.0727', '0.8325', '0.1278', '-0.538', '0.6543', '0.6816', '-0.0553', '-0.4731', '-0.3623', '-0.5596', '-0.673', '-0.086', '-0.2202', '-0.444', '0.02509', '0.04044', '-0.007446', '-0.11774', '0.2917', '0.1019', '0.301', '0.2062', '-0.3252', '0.3767', '-0.2048', '0.3901', '-0.0798', '-0.2576', '0.05212', '0.1616', '-0.3047', '0.5034', '-0.03677', '-0.3474', '0.10364', '0.3276', '-0.672', '0.1826', '-0.4255', '0.1846', '0.7163', '-0.1866', '-0.1677', '-0.00591', '-0.1473', '0.05576', '-0.2135', '0.2947', '-0.08466', '-0.3467', '-0.1888', '0.4006', '0.1716', '0.0386', '-0.2654', '-0.802', '0.181', '0.3005', '0.316', '-0.1869', '0.889', '0.00193', '0.2869', '0.3665', '0.12445', '0.2686', '0.7646', '-0.1569', '1.097', '-0.2153', '-0.1499', '-0.1123', '-0.701', '0.436', '0.2397', '0.2598', '-0.2563', '-0.1732', '-0.404', '0.8125', '0.2136', '-0.2247', '-0.2015', '-0.5474', '0.635', '0.3572', '0.3376', '-0.2262', '0.09955', '-0.244', '-0.3965']",C26845,0002508,D010300,332.0,,,
mondo:0005181,progressive external ophthalmoplegia,"['chronic progressive external ophthalmoplegia', 'progressive external ophthalmoplegia', 'chronic progressive external ophthalmoplegia [ambiguous]']",12558,,520820,,,,0002509,D017246,378.72,H49.4,,0000590
mondo:0005182,serous cystadenofibroma,,7320,,,,,C40032,0002510,,,,,
mondo:0005183,ovarian cystadenoma,"['ovary cystadenoma', 'benign cystadenoma of the ovary', 'cystadenoma of ovary', 'cystadenoma of the ovary', 'ovarian cystadenoma', 'benign ovarian cystadenoma', 'cystoma serosum simplex', 'simple cystoma of ovary', 'simple ovarian cystoma', 'simple cystoma of the ovary', 'benign cystadenoma of ovary']",3269,,,C0346169,,C4060,0002511,,620.2,,,
mondo:0005184,pancreatic ductal adenocarcinoma,"['ductal adenocarcinoma of the pancreas', 'pancreatic tubular adenocarcinoma', 'pancreatic ductal adenocarcinoma', 'pancreas ductal adenocarcinoma', 'pancreatic duct cancer', 'pancreatic ductal carcinoma', 'malignant neoplasm of duct of Wirsung', 'pancreatic duct adenocarcinoma', 'ductal adenocarcinoma of pancreas']",3587,,,C1335302,,C9120,0002517,D021441,157.3,,,
mondo:0005185,chronic childhood arthritis,"['Juvenile rheumatoid arthritis', 'Juvenile rheumatoid arthritis (AQ)', 'JRA']",6776,,,,"['0.3076', '0.06903', '0.0004828', '0.2351', '0.337', '-0.81', '0.2817', '-0.0718', '-0.9062', '0.1012', '0.11743', '0.0324', '0.03543', '0.546', '0.1603', '-0.363', '0.01095', '0.2656', '-0.4656', '-0.06235', '0.4185', '0.10474', '0.484', '-0.738', '-0.2585', '0.4517', '-0.3862', '-0.04272', '0.02103', '0.261', '0.1975', '-0.4329', '0.661', '0.0711', '0.932', '0.3232', '-1.145', '-0.05624', '0.3792', '0.272', '0.0281', '-0.3118', '-0.585', '0.778', '0.4731', '0.3452', '0.125', '-0.3384', '0.3972', '0.1879', '-0.3103', '-0.2122', '0.7095', '0.7676', '0.2114', '-0.9478', '-0.3076', '0.114', '-0.7983', '-0.7656', '0.505', '0.2607', '-0.422', '0.1432', '-0.1164', '0.3035', '0.02002', '0.592', '-0.4773', '0.1027', '0.1926', '-0.3342', '-0.1002', '-0.7036', '-0.2373', '0.8423', '-0.497', '1.487', '-0.464', '-0.3438', '-0.2373', '-0.2551', '-0.567', '0.488', '-0.2622', '0.2815', '-0.2125', '0.628', '0.686', '0.2964', '-0.2686', '0.0869', '-0.3909', '0.5664', '0.5454', '0.4392', '0.5044', '-0.7417', '-0.6357', '-0.5566']",C27179,0002609,,,,,
mondo:0005186,cocaine dependence,['cocaine addiction'],9975,,,,,C34492,0002610,,304.20,,,
mondo:0005187,human herpesvirus 8 infection,"['HHV8 infection', 'Human Herpesvirus 8 infection', 'Human Herpes Virus 8 infection']",,,,C1512508,,C39291,0002612,,,,,
mondo:0005188,iatrogenic Kaposi^s sarcoma,"['iatrogenic Kaposi^s sarcoma', 'iatrogenic Kaposi sarcoma']",,,,C1334149,,C35873,0002613,,,,,
mondo:0005189,internal carotid artery stenosis,,,,,,,,0002615,,433.10,,,
mondo:0005190,macroglobulinemia,['primary macroglobulinemia'],9080,,,C0024419,,C80307,0002616,D008258,273.3,C88.0,,
mondo:0005191,metastatic melanoma,['metastatic melanoma'],,,,C0278883,,C8925,0002617,,,,,
mondo:0005192,exocrine pancreatic carcinoma,"['exocrine cancer', 'pancreas cancer', 'pancreas carcinoma', 'exocrine pancreas carcinoma', 'carcinoma of pancreas', 'pancreatic cancer (not islets)', 'pancreatic carcinoma, familial', 'pancreatic cancer', 'carcinoma of exocrine pancreas', 'cancer of pancreas', 'cancer of the pancreas', 'carcinoma of the pancreas', 'pancreatic carcinoma']",4905,,,C0235974,"['-0.10236', '0.2155', '0.03568', '0.1134', '0.099', '-0.0815', '0.02583', '0.067', '0.02013', '-0.07983', '-0.1219', '-0.1254', '-0.085', '0.1127', '-0.2822', '-0.2255', '-0.05478', '-0.087', '0.084', '-0.2732', '-0.01593', '-0.1775', '0.1438', '-0.1741', '0.10895', '-0.07324', '0.006523', '0.0595', '-0.02147', '-0.2104', '0.1583', '0.01572', '0.1241', '-0.08405', '-0.013565', '-0.02954', '-0.0981', '0.04224', '-0.04254', '-0.05142', '-0.1065', '-0.148', '0.0727', '-0.0782', '-0.06335', '-0.08984', '-0.00922', '-0.05502', '0.0781', '-0.00782', '0.02667', '0.01654', '0.1087', '0.1404', '-0.1343', '-0.04868', '0.1841', '-0.0795', '-0.295', '0.00822', '0.2473', '0.0964', '-0.05988', '0.002203', '0.1039', '0.05774', '0.2415', '0.2413', '-0.1757', '0.1375', '0.001102', '-0.01525', '0.112', '0.002392', '0.06836', '-0.00677', '-0.0664', '-0.01851', '-0.0774', '-0.1713', '-0.2416', '0.07587', '-0.112', '-0.0697', '-0.1902', '-0.0861', '0.06714', '0.1083', '0.2391', '-0.1421', '0.1228', '0.2106', '0.0428', '-0.0901', '0.3647', '-0.002657', '0.10895', '-0.3352', '-0.09894', '0.1443']",C3850,0002618,,,,,
mondo:0005193,prostate intraepithelial neoplasia,"['prostatic intraepithelial neoplasia', 'prostate intraepithelial neopl.', 'pin - prostatic intraepithelial neoplasia', 'pin', 'prostate intraepithelial neoplasia (pin)']",,,,C0282612,,C4064,0002621,D019048,,,,
mondo:0005194,Rotavirus infection,['Rotavirus caused disease or disorder'],,,,C0035869,,,0002622,D012400,078.89,,,
mondo:0005195,septic peritonitis,,,,,,,,0002623,,,,,
mondo:0005197,thymus neoplasm,"['tumor of the Thymus', 'tumour of thymus', 'tumor of Thymus', 'THYMUS', 'thymic tumor', 'thymic neoplasm', 'thymus tumor', 'Thymus neoplasm', 'neoplasm of the Thymus', 'tumour of the Thymus', 'thymic tumour', 'neoplasm of thymus', 'thymus tumour', 'Thymus tumour', 'Thymus tumor', 'tumour of Thymus', 'tumor of thymus', 'thymus neoplasm (disease)', 'neoplasm of Thymus']",,,100100,C3714644,,C3412,0002626,,239.89,,,
mondo:0005198,vulvar intraepithelial neoplasia,"['vulvar intraepithelial tumor', 'intraepithelial neoplasia of the vulva', 'VIN', 'intraepithelial neoplasia of vulva', 'vulval intraepithelial neoplasia', 'squamous vulvar intraepithelial neoplasia', 'vulvar intraepithelial tumour', 'vulva intraepithelial neoplasia']",,,137583,C0346210,,C4756,0002627,,,,,
mondo:0005200,viral dilated cardiomyopathy,['Viruses caused dilated cardiomyopathy'],,,,C0264797,,,0002629,,,,,
mondo:0005201,restrictive cardiomyopathy,"['cardiomyopathy, constrictive', 'familial restrictive cardiomyopathy', 'primary restrictive cardiomyopathy', 'restrictive cardiomyopathy']",397,,217632,C0007196,,C62798,0002630,D002313,425.4,,10038748,
mondo:0005202,atopic IgE-mediated allergic disorder,['Atopic allergy'],,,,C1706410,,,0002686,,995.3,,,
mondo:0005203,ischemia reperfusion injury,,,,,,,,0002687,D015427,,,,
mondo:0005204,primary antiphospholipid syndrome,,,,,C0409980,,,0002689,,795.79,,,
mondo:0005206,renal carcinoma,"['kidney (renal) cancer', 'kidney cancer', 'renal carcinoma', 'renal cancer', 'kidney carcinoma', 'kidney (including renal cell) cancer', 'carcinoma of kidney']",4451,,,C1378703,"['-0.06085', '0.003557', '-0.05167', '-0.07007', '-0.01738', '-0.0444', '0.0861', '0.5195', '-0.1315', '0.07184', '-0.1101', '-0.1138', '-0.1957', '0.2284', '-0.3962', '-0.1769', '0.11865', '-0.1549', '0.1316', '-0.2089', '-0.0694', '-0.213', '0.2094', '-0.153', '0.3013', '-0.2275', '-0.0322', '0.214', '-0.12274', '0.01593', '0.265', '-0.3547', '0.397', '-0.06415', '0.1464', '-0.0606', '-0.2927', '-0.1536', '-0.11365', '0.0584', '-0.073', '-0.1077', '0.1044', '-0.2236', '0.10345', '-0.1272', '-0.2856', '-0.06866', '0.0592', '0.1243', '0.1473', '0.1118', '0.0905', '0.1041', '-0.1704', '0.0006886', '0.1113', '-0.004448', '-0.4814', '0.0219', '0.4055', '0.0557', '-0.191', '-0.0919', '-0.0434', '-0.04944', '0.3652', '0.43', '0.08905', '0.3281', '0.06396', '-0.06192', '0.1411', '0.00807', '0.0892', '-0.001702', '-0.02527', '0.007507', '-0.03165', '-0.3823', '-0.5435', '-0.02951', '0.00778', '-0.06226', '-0.2109', '-0.1788', '0.214', '-0.02382', '0.3076', '-0.1874', '0.1065', '0.1711', '0.038', '-0.09784', '0.4766', '-0.0271', '0.3855', '-0.347', '-0.1704', '0.132']",C9384,0002890,,,,,
mondo:0005207,choriocarcinoma,"['choriocarcinoma, malignant', 'chorioepithelioma', 'chorionic carcinoma', 'choriocarcinoma (disease)', 'chorion carcinoma', 'choriocarcinoma', 'chorioblastoma']",3594,,,C0008497,,C2948,0002893,D002822,,,,0100768
mondo:0005208,amelanotic skin melanoma,"['amelanotic malignant melanoma (of skin)', 'amelanotic malignant melanoma of skin', 'amelanotic cutaneous (skin) melanoma', 'amelanotic melanoma of skin', 'skin amelanotic malignant melanoma', 'amelanotic skin melanoma', 'amelanotic malignant melanoma of the skin', 'amelanotic melanoma of the skin', 'amelanotic malignant skin melanoma', 'amelanotic melanoma of zone of skin', 'skin amelanotic melanoma', 'zone of skin amelanotic melanoma']",10054,,,C0349515,,C4633,0002894,,,,,
mondo:0005210,uterine corpus sarcoma,"['sarcoma of the corpus uteri', 'body of uterus sarcoma', 'uterine sarcoma/mesenchymal', 'sarcoma of uterus', 'sarcoma of the uterine body', 'sarcoma of the uterus', 'sarcoma of corpus uteri', 'corpus uteri sarcoma', 'sarcoma of uterine body', 'uterine body sarcoma', 'uterine sarcoma', 'sarcoma of uterine corpus', 'sarcoma of the uterine corpus', 'uterus sarcoma', 'sarcoma of the body of uterus', 'sarcoma of body of uterus']",5165,,213620,C0338113,,C6339,0002914,,,,10039497,
mondo:0005211,ovarian serous adenocarcinoma,"['serous adenocarcinoma of ovary', 'ovarian serous adenocarcinoma', 'serous carcinoma of ovary', 'ovary serous adenocarcinoma', 'serous adenocarcinoma of the ovary', 'ovarian serous carcinoma', 'serous carcinoma of the ovary', 'serous ovarian cancer', 'malignant ovarian serous tumour']",5744,,,,,C7550,0002917,,,,,
mondo:0005212,rhabdomyosarcoma,"['rhabdomyosarcoma (disease)', 'rhabdomyosarcoma, malignant', 'rhabdomyosarcoma']",3247,,780,C0035412,,C3359,0002918,D012208,171.9,,10039022,0002859
mondo:0005213,uterine carcinoma,"['uterus carcinoma', 'carcinoma of uterus']",,,,C2960452,,,0002919,,,,,
mondo:0005214,vulva sarcoma,"['sarcoma of mammalian vulva', 'mammalian vulva sarcoma', 'vulvar sarcoma', 'sarcoma of vulva']",2096,,,C0238525,,C40317,0002920,,,,,
mondo:0005215,vulvar carcinoma,"['cancer of vulva', 'carcinoma of mammalian vulva', 'vulvar cancer', 'vulva carcinoma', 'mammalian vulva carcinoma', 'vulva cancer', 'carcinoma of vulva', 'cancer of the vulva', 'carcinoma of the vulva', 'vulvar carcinoma']",1294,,494418,C0677055,,C4866,0002921,,,,,
mondo:0005216,hypopharyngeal carcinoma,"['hypopharyngeal carcinoma', 'carcinoma of hypopharynx', 'hypopharynx carcinoma', 'carcinoma of the hypopharynx', 'cancer of the hypopharynx', 'hypopharyngeal cancer', 'cancer of hypopharynx', 'hypopharyngeal throat cancer']",,,,,,C9465,0002938,,,,,
mondo:0005217,familial cardiomyopathy,['hereditary cardiomyopathy'],,,,C0264789,"['0.3396', '-0.7114', '-0.1298', '0.604', '0.12317', '-0.6323', '0.564', '0.749', '-0.289', '-0.4204', '0.5137', '-0.1915', '-0.4429', '0.401', '-0.635', '0.2566', '-0.677', '-0.1368', '-0.7505', '-0.8135', '0.2976', '0.4092', '0.632', '-0.326', '0.4077', '-0.1827', '0.2915', '0.3513', '-0.05493', '-0.2593', '0.6426', '-0.3801', '0.8027', '0.267', '0.1843', '-0.4678', '-0.3203', '-0.531', '0.751', '-0.6914', '0.132', '0.692', '0.033', '0.657', '0.2316', '0.28', '0.3467', '0.576', '0.7217', '-0.431', '-0.3064', '0.1897', '0.5513', '0.04498', '0.4216', '-0.5625', '-0.3008', '0.415', '-0.8345', '-0.287', '0.0794', '0.57', '0.4934', '-1.015', '-0.925', '0.42', '0.3079', '0.5024', '-0.665', '0.216', '-0.3765', '0.3481', '0.00834', '-0.3127', '-0.0902', '0.8394', '-0.3662', '0.1978', '-0.3167', '0.3137', '-0.03104', '-0.2874', '-0.06158', '-0.541', '1.218', '-0.2686', '0.3843', '-0.068', '0.666', '0.2693', '0.01897', '-0.10895', '-0.2189', '0.2325', '0.9927', '1.114', '-0.01585', '-0.604', '-0.2627', '-0.264']",,0002945,,425.4,,,
mondo:0005219,breast fibrocystic disease,"['fibrocystic disease of breast', 'fibrocystic breast disease', 'mammary dysplasia', 'fibrocystic breast changes', 'diffuse cystic mastopathy', 'cystic disease of breast', 'breast fibrocystic change', 'benign breast disease', 'fibrocystic breast', 'fibrocystic disease of the breast', 'fibrocystic change of breast', 'fibrocystic mastopathy', 'cystic disease of the breast', 'fibrocystic change of the breast', 'fibrocystic disease']",10354,,,C0016034,,C3039,0003014,D005348,610.1,,,
mondo:0005220,collecting duct carcinoma,"['collecting duct renal cancer', 'carcinoma of renal collecting duct', 'collecting duct renal cell carcinoma', 'renal collecting duct carcinoma', 'collecting duct carcinoma', 'collecting duct carcinoma of the kidney', 'renal medullary carcinoma', 'carcinoma of the collecting ducts of Bellini', 'Bellini’s duct carcinoma', 'Bellini duct carcinoma', 'collecting duct of renal tubule carcinoma', 'kidney collecting duct carcinoma', 'carcinoma of kidney collecting duct', 'carcinoma of the renal collecting duct', 'Bellini carcinoma', 'cDC', 'renal carcinoma, collecting duct type', 'BDC', 'carcinoma of the kidney collecting duct', 'carcinoma of collecting ducts of Bellini', 'carcinoma of collecting duct of renal tubule']",4464,,247203,C1266044,,C6194,0003016,,,,,
mondo:0005221,renal pelvis urothelial carcinoma,"['kidney renal pelvis urothelial cancer', 'renal pelvis urothelial cancer', 'urothelial cell carcinoma of the renal pelvis', 'transitional cell carcinoma of the renal pelvis', 'transitional cell carcinoma of renal pelvis', 'renal pelvis transitional cell carcinoma', 'renal pelvis urothelial carcinoma', 'urothelial cell carcinoma of renal pelvis']",5974,,,C0238410,,C7355,0003017,,189.0,,,
mondo:0005223,acute myeloid leukemia with minimal differentiation,"['M0 acute myelogenous leukemia', 'AMLMD', 'minimally differentiated acute myeloblastic leukaemia', 'AML M0', 'AML with minimal differentiation', 'acute myeloblastic leukemia with minimal differentiation', 'M0 myeloid leukaemia with minimal differentiation', 'M0 acute myelogenous leukaemia', 'M0 acute myelocytic leukemia', 'acute myeloid leukemia with minimal differentiation', 'acute myeloid leukemia, minimally differentiated', 'M0 acute granulocytic leukaemia with minimal differentiation', 'M0 acute myelocytic leukaemia', 'acute myelogenous leukemia with minimal differentiation', 'M0 myeloid leukemia with minimal differentiation', 'M0 acute myeloblastic leukemia', 'M0 myeloid leukaemia', 'acute myeloid leukemia with minimal differentiation (MO)', 'acute myeloblastic leukemia, minimally differentiated', 'acute myelogenous leukaemia with minimal differentiation', 'M0 acute myelogenous leukemia with minimal differentiation', 'M0 acute granulocytic leukemia with minimal differentiation', 'minimally differentiated acute myeloblastic leukemia', 'M0 acute granulocytic leukaemia', 'M0 myeloid leukemia', 'M0 acute myelogenous leukaemia with minimal differentiation', 'acute myelocytic leukemia with minimal differentiation', 'M0 acute granulocytic leukemia', 'acute myelocytic leukaemia with minimal differentiation', 'M0 acute myeloblastic leukaemia', 'acute myeloblastic leukaemia with minimal differentiation', 'acute myeloid leukaemia with minimal differentiation (MO)']",0081085,,98832,C0522631,,C8460,0003026,,,,,
mondo:0005224,acute myeloblastic leukemia without maturation,"['M1 acute myeloid leukaemia without maturation', 'acute granulocytic leukaemia without maturation', 'acute myeloblastic leukemia M1', 'acute M1 myeloid leukaemia', 'acute M1 myeloid leukemia', 'acute myelogenous leukemia without maturation', 'acute myelocytic leukemia without maturation', 'acute myeloblastic leukemia type 1', 'M1 acute myeloblastic leukaemia without maturation', 'M1 acute myeloid leukaemia', 'AWM', 'M1 acute myelocytic leukaemia', 'M1 acute granulocytic leukaemia without maturation', 'M1 acute myelocytic leukaemia without maturation', 'M1 acute myelogenous leukemia without maturation', 'M1 acute myelogenous leukaemia without maturation', 'M1 acute granulocytic leukaemia', 'M1 acute myeloid leukemia', 'acute myeloid leukemia without maturation', 'M1 acute myelogenous leukaemia', 'AML without maturation', 'acute myeloid leukaemia without maturation', 'M1 acute myelocytic leukemia', 'M1 acute granulocytic leukemia', 'acute myeloid leukemia without maturation (FAB M1)', 'acute myelogenous leukaemia without maturation', 'acute myeloblastic leukaemia M1', 'acute myelocytic leukaemia without maturation', 'acute myeloblastic leukaemia type 1', 'M1 acute myelocytic leukemia without maturation', 'AML M1', 'M1 acute granulocytic leukemia without maturation', 'M1 acute myeloblastic leukemia', 'M1 acute myeloid leukemia without maturation', 'M1 acute myeloblastic leukaemia', 'acute myeloid leukaemia without maturation (FAB M1)', 'M1 acute myelogenous leukemia', 'acute granulocytic leukemia without maturation', 'M1 acute myeloblastic leukemia without maturation', 'FAB M1']",0081086,,98833,,,C3249,0003027,,,,,
mondo:0005227,abscess,['abscess (disease)'],,,,C0000833,,C26686,0003030,D000038,682.9,,,
mondo:0005229,bacterial infectious disease with sepsis,"['Bacteremias', 'bacteremia', 'symptomatic bacteremia', 'bacterial sepsis']",0040085,,,C0004610,,,0003033,D016470,790.7,,,
mondo:0005230,cellulitis,"['cellulitis (disease)', 'cellulitis']",3488,,,,,C26715,0003035,D002481,682.9,,,0100658
mondo:0005231,hepatitis C virus infection,"['hepatitis Nona nonB', 'viral hepatitis C', 'Hepatitis C virus caused hepatitis', 'non-A, non-B Hepatitis', 'chronic hepatitis C', 'hepatitis C infection', 'hepatitis type C', 'NANBH']",1883,,,C0019196,,C3098,0003047,D006526,070.7,,,
mondo:0005232,large cell carcinoma,"['carcinoma, large cell', 'large cell carcinoma']",4552,,,C0206704,,C3780,,D018287,,,,
mondo:0005233,non-small cell lung carcinoma,"['NSCLC', 'non-small cell carcinoma of the lung', 'non-small cell cancer of the lung', 'non-small cell carcinoma of lung', 'non-small cell lung carcinoma (disease)', 'non-small cell lung carcinoma', 'non-small cell lung cancer', 'NSCLC - non-small cell lung cancer', 'non-small cell cancer of lung']",3908,,488201,C0007131,"['0.06113', '-0.011', '0.00868', '0.1693', '0.1028', '-0.2952', '0.2181', '0.11896', '-0.04492', '-0.1622', '0.1091', '-0.10565', '0.03418', '-0.0376', '-0.3887', '-0.251', '-0.01921', '-0.0772', '0.183', '-0.3062', '-0.06537', '-0.0643', '0.4563', '-0.3257', '0.4395', '-0.2732', '-0.01672', '0.0438', '-0.2306', '-0.3335', '0.4055', '0.1494', '0.3323', '-0.05405', '0.04095', '-0.05673', '-0.3638', '-0.0635', '-0.0955', '-0.002068', '-0.0668', '-0.337', '0.07043', '-0.1361', '0.06836', '-0.1277', '-0.1294', '0.01688', '0.1362', '-0.1504', '0.03583', '-0.0985', '0.00905', '0.2778', '-0.1931', '-0.1307', '0.1647', '0.1449', '-0.5186', '-0.01554', '0.04965', '0.03595', '-0.1132', '0.2251', '0.02478', '-0.07477', '0.3296', '0.188', '-0.0575', '0.592', '0.1259', '0.03433', '0.0426', '-0.04376', '0.1917', '-0.01964', '-0.1573', '-0.412', '-0.1248', '-0.2249', '-0.336', '0.1942', '-0.2446', '0.1322', '-0.505', '-0.251', '0.3416', '0.0913', '0.2832', '-0.1798', '0.00367', '0.2126', '0.01415', '-0.1315', '0.371', '0.2177', '0.03326', '-0.171', '-0.1711', '-0.01903']",C2926,0003060,D002289,,,,0030358
mondo:0005235,smoldering plasma cell myeloma,"['smoldering Multiple myeloma/plasma cell myeloma', 'smouldering multiple myeloma', 'smoldering plasma cell myeloma', 'smoldering multiple myeloma', 'smouldering myeloma', 'smoldering myeloma', 'asymptomatic myeloma', 'asymptomatic plasma cell myeloma', 'smouldering Multiple myeloma/plasma cell myeloma']",9551,,,,,C7149,0003073,,,,,
mondo:0005236,xanthoma,"['xanthoma', 'xanthoma (disease)']",,,,,,C4071,0003075,,,,,0001114
mondo:0005238,round cell liposarcoma,"['round cell liposarcoma', 'cellular myxoid liposarcoma', 'round cell liposarcoma (morphologic abnormality)']",5692,,,C0334471,,C4252,0003084,,171.9,,,
mondo:0005240,kidney disorder,"['nephropathy', 'disease of kidney', 'kidney disorder', 'renal disorder', 'renal disease', 'kidney disease or disorder', 'kidney disease', 'disorder of kidney']",557,,,C0022658,,C3149,0003086,D007674,583.81,,,
mondo:0005242,empyema,,,,,,,C34572,0003097,D004653,510,,,
mondo:0005244,peripheral neuropathy,"['peripheral nerve disorder', 'neuropathy', 'peripheral neuropathy']",870,,,C0442874,"['0.4644', '0.1777', '-0.3445', '0.538', '0.062', '-0.04144', '-0.142', '-0.12476', '-0.1884', '0.06696', '0.1981', '-0.1389', '0.10864', '0.6685', '-0.253', '0.3904', '-0.2153', '0.1086', '-0.755', '-0.1917', '0.629', '-0.5737', '0.0728', '0.2695', '0.02545', '-0.085', '-0.05927', '-0.4375', '-0.0979', '-0.9478', '0.219', '0.2383', '0.2277', '-0.4631', '0.2031', '-0.1204', '-0.295', '-0.4192', '0.2634', '-0.5337', '-0.62', '-0.3875', '-0.2214', '0.39', '-0.0914', '-0.6226', '0.3118', '0.1285', '0.6904', '0.4006', '-0.648', '0.2783', '0.2786', '0.2683', '-0.2289', '-0.3315', '0.308', '-0.2598', '-0.95', '-0.62', '-0.3906', '0.3123', '-0.3354', '0.5884', '-0.279', '0.4578', '0.1421', '0.9795', '-0.1562', '0.3857', '0.00974', '0.4797', '-0.166', '-1.061', '0.515', '0.3193', '0.00586', '0.627', '-0.00856', '0.1974', '-0.549', '-0.4045', '-0.05026', '0.266', '-0.2258', '0.0825', '0.3113', '0.3003', '0.4937', '-0.00554', '0.2438', '0.1289', '-0.3875', '-0.09595', '-0.03592', '0.1768', '-0.7925', '0.004562', '0.174', '-0.02122']",C4731,0004149,,,,10034606,
mondo:0005246,osteomyelitis,"['osteomyelitis', 'osteomyelitis (disease)']",1019,,,C0029443,,C27577,0003102,D010019,730.97,,,0002754
mondo:0005247,bacterial urinary tract infection,"['UTI', 'urinary tract infectious disease', 'bacterial urinary tract infection (disease)', 'tract, infection of urinary', 'infection, urinary tract', 'urinary tract infection']",,,,,,C50791,0003103,,599.0,,,
mondo:0005249,pneumonia,['acute pneumonia'],552,,,C0032285,,C3333,0003106,D011014,486,J18.9,,
mondo:0005250,placental villitis,,,,,C1270169,,,0003110,,,,,
mondo:0005252,heart failure,"['heart failure', 'insufficiency, Cardiac', 'cardiac failure', 'cardiac insufficiency', 'failure, heart']",,,,CN236639,,C50577,0003144,D006333,428.9,,,
mondo:0005253,high output heart failure,,,,,C0221045,,,0003145,,,,,
mondo:0005254,symptomatic heart failure,,,,,,,,0003146,,,,,
mondo:0005255,mild heart failure,,,,,,,,0003147,,,,,
mondo:0005256,moderate heart failure,,,,,,,,0003148,,,,,
mondo:0005257,advanced heart failure,,,,,,,,0003149,,,,,
mondo:0005258,autism spectrum disorder,"['pervasive developmental disorders', 'atypical autism', 'autistic spectrum disorder', 'pervasive developmental disorder - not otherwise specified']",0060042,,106,,"['0.1498', '0.2563', '0.228', '0.2474', '0.04968', '-0.4065', '0.4658', '0.7188', '-0.4338', '-0.392', '0.996', '0.1809', '0.063', '0.4714', '0.3496', '0.3484', '-0.499', '-0.2607', '-0.2659', '-0.654', '-0.321', '-0.3376', '0.01222', '-0.3726', '0.4365', '-0.5635', '-0.03403', '0.05957', '0.1888', '-0.2803', '0.6187', '-0.1996', '1.105', '0.557', '-0.04034', '0.09344', '0.09924', '0.453', '0.5264', '-0.5083', '0.564', '-0.005543', '-0.7437', '-0.371', '0.701', '-1.305', '0.05762', '-0.316', '-0.1276', '0.0914', '-0.581', '-0.07306', '-0.697', '0.0895', '1.0', '0.149', '-0.7734', '0.5234', '-0.04117', '0.5103', '0.0975', '0.2357', '0.3137', '0.628', '-0.406', '0.1669', '0.832', '-0.002275', '-0.5356', '0.4702', '0.338', '0.145', '-0.3296', '-0.5845', '0.681', '0.3218', '-0.3564', '0.675', '-0.1771', '-0.2305', '0.5244', '0.3787', '-0.4004', '0.3809', '0.3535', '0.06573', '-0.4797', '0.2148', '0.4622', '0.67', '-0.3538', '0.0848', '-1.046', '0.1473', '-0.1785', '0.549', '-0.00707', '-0.639', '0.3862', '-0.1642']",C88412,0003759,,,,,
mondo:0005259,Asperger syndrome,"['ASPG', 'asperger syndrome, susceptibility to', 'autism spectrum disorder without disorder of intellectual development and with mild or no impairment of functional language']",0050432,,1162,,"['0.04208', '0.2803', '0.3384', '0.09534', '-0.1923', '-0.3113', '0.4072', '0.4116', '-0.3694', '-0.03946', '-0.1139', '-0.03116', '0.2334', '0.05692', '0.3481', '-0.1715', '-0.0653', '-0.11145', '-0.3914', '-0.571', '-0.1142', '0.002487', '0.1975', '-0.2155', '0.3042', '-0.1868', '0.05017', '0.0773', '-0.2817', '-0.10754', '0.318', '-0.009674', '0.3523', '0.1368', '-0.08594', '0.1675', '-0.02391', '-0.09186', '-0.1115', '-0.3606', '0.5093', '-0.3115', '-0.2715', '-0.10876', '0.3628', '-0.3215', '0.02335', '-0.03735', '-0.08716', '0.516', '-0.2725', '0.2103', '-0.4934', '0.1234', '0.3215', '0.2113', '0.05997', '-0.0258', '-0.0676', '0.10223', '-0.0509', '-0.02127', '0.2085', '0.189', '0.09784', '0.123', '0.2006', '-0.06287', '-0.00411', '0.1953', '-0.2318', '0.04068', '-0.1263', '-0.0957', '0.1223', '0.1616', '0.1398', '-0.0297', '-0.2546', '-0.338', '0.2698', '-0.0925', '-0.1693', '0.4521', '0.04248', '0.0896', '-0.2042', '0.02875', '0.57', '0.2732', '-0.1174', '0.4058', '-0.11115', '-0.0635', '0.1267', '0.1141', '0.0832', '-0.1713', '0.05093', '-0.0881']",C97159,0003757,D020817,,,,
mondo:0005260,autism,"['infantile autism', 'autism spectrum disorder', 'autistic disorder of childhood onset', 'autism (disease)', 'autistic disorder', 'childhood autism', 'Kanner^s syndrome', 'autism, susceptiblity to', 'autism']",12849,209850,,,"['-0.171', '0.3933', '0.2754', '-0.1197', '0.05682', '-0.3508', '0.3315', '0.627', '-0.336', '0.01685', '-0.1509', '-0.187', '0.2842', '0.3018', '0.4634', '0.1442', '-0.04645', '-0.2405', '-0.414', '-0.7124', '-0.1365', '-0.0626', '0.1209', '-0.0177', '0.114', '-0.225', '0.2688', '0.3735', '-0.3918', '0.1974', '0.2426', '-0.05426', '0.6514', '0.293', '-0.05237', '-0.005825', '-0.2236', '-0.0962', '0.1761', '-0.633', '0.48', '-0.506', '-0.0772', '0.003431', '0.02254', '-0.799', '0.02246', '0.02164', '0.08466', '0.571', '-0.2666', '0.1707', '-0.2827', '0.1189', '0.2164', '0.2878', '-0.218', '-0.22', '-0.2874', '-0.2001', '-0.1805', '0.1857', '0.10596', '0.1268', '-0.0388', '0.3386', '0.413', '0.0794', '0.1329', '-0.1658', '-0.2462', '0.1353', '-0.1959', '-0.0008736', '0.4067', '0.1627', '0.3535', '0.0857', '-0.1567', '-0.6147', '0.13', '0.4878', '-0.0451', '0.406', '0.3118', '-0.0549', '-0.2656', '0.2141', '0.3015', '0.03796', '-0.10876', '0.5596', '-0.117', '0.00797', '-0.0003326', '0.1772', '-0.04703', '-0.1707', '0.03812', '0.1377']",C97161,0003758,D001321,299.0,,,0000717
mondo:0005262,central nervous system cyst,"['cyst of Central nervous system', 'cyst, suprasellar', 'cleft cysts, Rathke^s', 'cysts, central nervous system', 'suprasellar cyst', 'cysts, suprasellar', 'CNS cyst', 'cysts, Rathke cleft', 'cyst of the Central nervous system', 'central nervous system cyst (disease)', 'cyst of CNS', 'Rathke cleft cysts', 'suprasellar cysts', 'Rathke^s cleft cysts', 'central nervous system cyst', 'Rathkes cleft cysts', 'cyst of the CNS']",,,,C0349606,,C4657,0003760,D020863,,,,0030724
mondo:0005264,transient ischemic attack,"['attack, transient ischemic', 'ischemic attack, transient', 'transient cerebral ischaemia', 'transient cerebral ischemia', 'ischaemic attack, transient', 'transient ischaemic attack (disease)', 'TIA', 'transient ischemic attack (disease)', 'transient cerebral ischemia (disorder) [ambiguous]', 'transient ischemic attack', 'transient ischemic attacks', 'TIA - transient ischaemic attack', 'attack, transient ischaemic', 'transient ischaemic attacks', 'TIA - transient ischemic attack']",224,,,,,C50781,0003764,D002546,435.9,,,0002326
mondo:0005265,inflammatory bowel disease,"['IBD', 'autoimmune bowel disorder', 'inflammatory bowel disease']",0050589,,,C0021390,"['0.1287', '0.1346', '-0.1035', '0.56', '0.01845', '-0.01872', '0.311', '0.3528', '-0.361', '-0.1288', '0.201', '-0.12195', '-0.3684', '0.6978', '-0.6577', '-0.5513', '-0.2406', '0.2786', '-0.0637', '-0.988', '0.5356', '-0.392', '-0.2329', '-0.214', '0.05215', '-0.377', '-0.1621', '0.4575', '0.942', '-0.1124', '0.3606', '-0.6733', '-0.07135', '0.01958', '0.7256', '0.1797', '-0.928', '-0.4463', '0.523', '0.03568', '0.11725', '0.0451', '0.06635', '0.0973', '0.217', '-0.06226', '0.2103', '-0.2903', '0.445', '0.5044', '-0.4822', '-0.2898', '0.11993', '-0.04315', '-0.3452', '0.25', '-0.7134', '0.3125', '-0.4128', '-0.1007', '0.2922', '0.356', '0.462', '-0.2869', '0.1979', '0.194', '0.9224', '0.0324', '0.02274', '1.002', '0.1055', '0.1395', '0.2471', '0.00875', '0.1259', '0.41', '0.4346', '0.77', '0.1943', '-0.428', '-0.317', '-0.3267', '-0.2825', '-0.1759', '0.02875', '-0.5293', '0.2205', '0.091', '0.4673', '-0.03638', '0.1165', '-0.3333', '0.0724', '0.1724', '0.62', '0.2725', '-0.438', '-0.2019', '-0.4407', '-0.2441']",C3138,0003767,D015212,558.9,,,
mondo:0005266,diabetic retinopathy,['retinal abnormality - diabetes-related'],8947,,,C0011884,"['-0.05206', '0.112', '0.3098', '0.4973', '-0.0418', '-0.3315', '-0.0958', '0.843', '-0.394', '0.291', '-0.6343', '-0.1365', '0.2205', '0.4302', '-0.53', '-0.5205', '0.3105', '0.417', '0.474', '-0.8286', '0.087', '-0.1497', '-0.3413', '-0.04407', '-0.2576', '0.01092', '-0.03696', '0.03876', '0.3303', '0.319', '0.653', '-0.0761', '0.06744', '0.1031', '-0.3865', '0.4387', '0.1295', '-0.0588', '0.5156', '-0.7764', '0.4827', '-0.1653', '0.2341', '0.3281', '0.03983', '0.1317', '-0.353', '-0.2979', '0.3928', '-0.529', '0.3381', '-0.09174', '0.524', '-0.603', '0.582', '0.1709', '0.452', '0.1619', '-0.932', '-0.3284', '-0.4805', '-0.0786', '-0.1407', '0.0072', '-0.2651', '0.346', '0.418', '0.6714', '-0.3062', '0.683', '0.4514', '0.418', '-0.003588', '-0.157', '0.268', '0.0953', '0.0705', '0.6055', '0.0488', '-0.04895', '-0.2566', '-0.2576', '-0.5835', '0.2654', '0.1495', '0.02556', '0.426', '-0.01855', '0.5635', '0.2495', '0.02563', '0.2761', '-0.883', '0.65', '0.4897', '0.006756', '-0.3748', '-0.4966', '-0.5425', '0.5605']",C34538,0003770,D003930,362.0,,,
mondo:0005267,heart disorder,"['heart disease or disorder', 'cardiac disease', 'heart disorder', 'heart disease', 'disease of heart', 'disorder of heart', 'heart/pericardial disease or disorder', 'heart/pericardial disorder', 'heart trouble', 'heart/pericardial disease', 'disorder of heart/pericardium', 'heart/pericardial trouble']",114,,,CN239852,,C3079,0003777,D006331,V47.2,,,
mondo:0005269,carotid artery disorder,"['carotid artery segment disease or disorder', 'disorder of carotid artery', 'carotid artery segment disease', 'carotid artery disorder', 'disorder of carotid artery segment', 'disease of carotid artery segment']",3407,,,C0007273,,C84476,0003781,D002340,447.9,,,
mondo:0005271,allergic disease,"['type I hypersensitivity disease', 'hypersensitivity reaction type I disease', 'allergy', 'allergic reaction', 'allergic form of immune system disease', 'disorder of type I hypersensitivity', 'hypersensitivity', 'allergic response', 'allergic hypersensitivity disease', 'allergic form of disease or disorder']",1205,,,C1527304,,C114476,0003785,D006967,V15.09,,,
mondo:0005272,myelodysplastic syndrome with single lineage dysplasia,"['MDS-SLD', 'aregenerative anaemia', 'refractory anemia', 'MDS with single lineage dysplasia', 'RA', 'refractory anaemia', 'aregenerative anemia']",,,98826,C2826318,,C82591,0003802,D000753,238.72,,10038269,
mondo:0005275,lung disorder,"['lung disease', 'disease of lung', 'pulmonary diseases', 'pulmonary disorder', 'disorder of lung', 'lung disorders', 'pulmonary disorders', 'lung disease or disorder']",850,,,,,C3198,0003818,D008171,518.89,,,
mondo:0005276,dental caries,"['dental caries of smooth surface', 'dental caries extending into pulp', 'dental caries pit and fissure']",216,,,C0011334,,,0003819,D003731,521.07,K02,,
mondo:0005277,migraine disorder,"['migraine variant', 'migraine', 'migraine disorder', 'migraine with or without aura', 'migraine headache']",6364,,,,"['0.02495', '-0.2842', '-0.0896', '0.3691', '-0.1847', '-0.07196', '-0.0891', '-0.226', '-0.4133', '-0.5137', '0.105', '0.7197', '0.01831', '0.3647', '-0.5625', '-0.1127', '-0.1392', '0.3022', '-1.209', '-0.02615', '-0.3677', '-0.2695', '-0.0827', '-0.409', '-0.4678', '-0.622', '0.2644', '-0.4072', '-0.4995', '-0.384', '0.6396', '-0.37', '0.4033', '0.0449', '-0.2262', '0.3901', '-0.821', '-0.5884', '0.01808', '-0.479', '1.103', '-0.0222', '0.312', '-0.1453', '0.332', '-0.7056', '-0.5127', '0.1497', '-0.2291', '0.676', '-0.331', '0.1984', '-0.0735', '0.325', '0.996', '0.3083', '0.4067', '-0.1054', '-0.3945', '-0.02852', '-0.428', '0.2583', '0.0536', '-0.03023', '-0.6313', '0.5117', '0.4004', '1.113', '0.3528', '0.3384', '0.08075', '0.608', '0.4011', '-1.246', '0.2808', '0.755', '-0.2913', '1.164', '0.367', '-0.1324', '0.1528', '0.05276', '-0.0626', '-0.02043', '0.4443', '-0.12085', '0.5093', '0.1299', '0.943', '0.3235', '-0.2228', '-0.2095', '-0.002628', '-0.1903', '0.301', '0.2493', '-0.5303', '-1.043', '-0.191', '0.162']",C89715,0003821,D008881,346.9,,,
mondo:0005278,serous adenocarcinoma,"['serous cystadenocarcinoma', 'serous carcinoma', 'serous adenocarcinoma', 'serous cystadenocarcinoma, NOS (morphologic abnormality)']",3114,,,C0206701,,C40101,0003825,,,,,
mondo:0005279,pulmonary embolism,"['pulmonary artery embolism', 'embolism, pulmonary', 'pulmonary embolism', 'pulmonary embolus', 'pulmonary embolism (disease)']",9477,,,C0034065,,C50713,0003827,D011655,415.19,,,0002204
mondo:0005280,prostatitis,"['prostatitis (disease)', 'prostatitis', 'prostate gland inflammation']",14654,,,C0033581,,C26866,0003830,D011472,601.9,,,0000024
mondo:0005281,gallbladder disorder,"['disorder of gall bladder', 'Gall bladder disorder', 'disease of gall bladder', 'gallbladder disorder', 'gall bladder disease or disorder', 'gall bladder disease']",0060262,,,C0016977,,C34631,0003832,D005705,575.9,K82,,
mondo:0005282,cutaneous lupus erythematosus,"['lupus erythematosus, cutaneous']",0050169,,,C0024137,,C26819,0003834,D008178,,,,
mondo:0005283,retinal disorder,"['retinopathy', 'eye disease of retina', 'retina eye disease']",5679,,,C0035309,,C62601,0003839,D012164,362.9,,,
mondo:0005284,chronic progressive multiple sclerosis,,,,,C0393665,,,0003840,D020528,,,,
mondo:0005286,palatal neoplasm,"['secondary palate tumour', 'neoplasm of the palate', 'tumor of palate', 'neoplasm of palate', 'secondary palate neoplasm (disease)', 'tumour of the palate', 'tumor of the palate', 'palate neoplasm', 'secondary palate tumor', 'palate tumor', 'palate tumour', 'tumour of secondary palate', 'tumor of secondary palate', 'tumour of palate', 'neoplasm of secondary palate']",,,,C0030215,,C4402,0003849,D010157,,,,
mondo:0005287,developmental disability,,,,,,,,0003852,D002658,,,,
mondo:0005288,intestinal polyp,"['intestinal polyp', 'intestinal polyp (disease)']",,,,,,,0003855,D007417,569.89,,,0005266
mondo:0005289,paranasal sinus neoplasm,"['tumour of the accessory sinus', 'neoplasm of the accessory sinus', 'paranasal sinus tumor', 'tumor of paranasal sinus', 'accessory sinus tumour', 'paranasal sinus neoplasms', 'accessory sinus neoplasm', 'tumor of the accessory sinus', 'tumor of the paranasal sinus', 'tumour of accessory sinus', 'neoplasm of the paranasal sinus', 'accessory sinus tumor', 'neoplasm of accessory sinus', 'tumour of the paranasal sinus', 'neoplasm of paranasal sinus', 'paranasal sinus tumour', 'tumor of accessory sinus', 'paranasal sinus neoplasm (disease)', 'paranasal sinus neoplasm', 'tumour of paranasal sinus']",1350,,,C0030470,,C7488,0003866,,,,,0030072
mondo:0005291,brain aneurysm,"['intracranial aneurysm', 'brain aneurysm']",10941,,,C0007766,,,0003870,D002532,,,,
mondo:0005292,colitis,"['colon inflammation', 'colitis', 'colitis (disease)']",0060180,,,C0009319,,C26723,0003872,D003092,558.9,,,0002583
mondo:0005293,flatfoot,"['fallen Arch', 'flat Foot']",,,,,,C34616,0003874,D005413,734,,,
mondo:0005294,peripheral vascular disease,"['arterial occlusive disease', 'vascular disease, peripheral', 'disease, peripheral vascular', 'peripheral vascular disorder']",341,,,,,C35136,0003875,D016491,443.81,,,
mondo:0005295,intermittent vascular claudication,"['intermittent claudication', 'Charcot^s syndrome']",3669,,,C0021775,,,0003876,D007383,440.21,,,
mondo:0005296,sleep apnea syndrome,"['sleep apnea', 'sleep apnea, mixed central and obstructive', 'apneas, sleep', 'mixed sleep apnea', 'hypersomnia with periodic respiration', 'apnea syndrome, sleep', 'sleep apneas, mixed', 'sleep-disordered breathing', 'mixed central and obstructive sleep apnea', 'mixed sleep Apneas', 'breathing, sleep-disordered', 'sleep disordered breathing', 'sleep apneas', 'apnea syndromes, sleep', 'sleep hypopnea', 'sleep hypopneas', 'sleep apnea, mixed', 'hypopneas, sleep', 'sleep apnea syndrome', 'SDB', 'hypopnea, sleep', 'apnea, sleep']",0050847,,,,,C148023,0003877,D012891,780.57,G47.3,,0010535
mondo:0005297,urethritis,"['non-gonococcal urethritis', 'Nongonococcal urethritis', 'urethritis', 'urethritis (disease)', 'urethra inflammation']",1343,,,,,C26904,0003878,D014526,597.80,,,0500006
mondo:0005298,osteoporosis,"['osteoporosis, postmenopausal, susceptibility', 'osteoporosis, susceptibility to', 'fracture, hip, susceptibility to', 'bone mineral density variation QTL, osteoporosis', 'osteoporosis, involutional', 'osteoporosis, postmenopausal']",11476,166710,,,"['0.3638', '-0.1484', '0.2126', '0.698', '0.25', '-0.5', '-0.4983', '0.9795', '-0.74', '-0.3972', '0.2325', '0.5127', '0.00472', '0.586', '-0.402', '-0.2006', '-0.2876', '0.3726', '-0.719', '-0.1849', '-0.1793', '-0.5923', '0.3958', '-0.5405', '0.5376', '-0.351', '0.2261', '-0.782', '-0.5474', '-0.0476', '0.7036', '-0.6206', '-0.2708', '-0.3516', '-0.04108', '-0.2312', '-0.0642', '-0.7817', '0.4001', '-0.54', '0.1982', '-0.1171', '0.2524', '-0.3066', '0.635', '-0.5723', '0.151', '0.0904', '0.4836', '0.9663', '0.7114', '0.1265', '0.3823', '-0.186', '-0.4207', '-0.4697', '-0.3176', '0.432', '-0.495', '-0.1257', '0.1356', '0.274', '-1.051', '-0.6113', '-0.0566', '0.9497', '0.657', '0.725', '-0.4055', '-0.37', '0.6694', '-0.1791', '-0.11304', '-0.5986', '0.588', '0.6953', '-0.1659', '0.6836', '-0.1882', '-0.01988', '-0.08185', '-0.453', '0.3987', '0.5244', '-0.5986', '0.5234', '0.4958', '-0.0905', '1.286', '0.03445', '-0.5923', '-0.3132', '-1.108', '-0.2179', '0.6064', '-0.2876', '0.08014', '-0.5684', '-0.3906', '-0.3977']",C3298,0003882,D010024,733.09,M81,,
mondo:0005299,brain ischemia,"['ischemia cerebrovascular', 'brain ischemia', 'brain ischaemic disease', 'ischemic encephalopathy', 'ischaemic disease of brain', 'brain ischemic disease', 'ischemic disease of brain', 'cerebrovascular ischemia', 'ischaemic encephalopathy']",2316,,,C0007786,,C78394,0003883,D002545,348.89,,,
mondo:0005300,chronic kidney disease,"['chronic kidney disease', 'renal failure - chronic', 'CKD - chronic kidney disease', 'kidney disease, chronic', 'chronic renal insufficiency', 'chronic renal failure syndrome', 'chronic renal disease', 'CKD']",784,,,C0022661,,C80078,0003884,D007676,585.6,N18.9,,
mondo:0005301,multiple sclerosis,"['generalized multiple sclerosis', 'insular sclerosis', 'generalised multiple sclerosis']",2377,,802,C0026769,"['-0.1787', '-0.03452', '-0.2302', '0.1368', '0.10266', '-0.3926', '0.32', '-0.02821', '-0.248', '-0.0138', '0.2852', '-0.11206', '-0.2625', '0.544', '0.6504', '-0.3506', '-0.10803', '-0.1412', '-0.1722', '-0.1592', '-0.3', '-0.4565', '0.03152', '-0.07916', '-0.1967', '-0.2249', '0.0826', '0.1085', '-0.2695', '-0.2008', '0.1666', '-0.1063', '0.3032', '-0.3308', '0.4058', '-0.2386', '-0.433', '-0.435', '0.2966', '-0.2375', '0.1132', '-0.23', '0.04016', '0.1711', '0.1741', '-0.1836', '0.02061', '-0.3413', '-0.3943', '0.549', '-0.4114', '0.6274', '-0.1399', '-0.4514', '-0.437', '0.01785', '0.266', '0.03928', '0.04337', '-0.8086', '-0.1746', '0.1763', '0.1962', '0.6875', '-0.2391', '0.715', '0.6934', '0.8916', '-0.2013', '0.524', '0.4595', '-0.1114', '0.2375', '-0.597', '0.0488', '0.933', '-0.1161', '1.278', '-0.02661', '-0.3518', '-0.1247', '-0.5996', '-0.1403', '-0.04132', '0.3086', '0.01697', '0.01631', '0.4326', '0.542', '0.05768', '-0.0247', '-0.4187', '0.12415', '-0.0385', '0.4673', '-0.02257', '-0.711', '-0.1503', '-0.09045', '-0.2725']",C3243,0003885,D009103,340,G35,,
mondo:0005302,"attention deficit hyperactivity disorder, inattentive type","['hyperkinetic disorder', 'attention deficit hyperactivity disorder, predominantly inattentive type', 'attention deficit disorder', 'attention deficit hyperactivity disorder, inattentive/distractible type', 'ADHD', 'ADD']",1094,,,,"['-0.04446', '0.1431', '0.0919', '0.01341', '-0.085', '-0.2064', '0.0639', '0.08344', '-0.1271', '-0.01895', '-0.08496', '-0.12415', '0.3035', '0.1722', '-0.0341', '0.0572', '-0.075', '0.03253', '-0.1935', '-0.4062', '-0.2878', '0.004223', '0.04437', '-0.1343', '0.02592', '-0.0506', '0.01426', '-0.05988', '0.1449', '-0.004482', '-0.1165', '-0.11115', '0.1609', '0.1438', '-0.1948', '-0.1071', '0.05438', '-0.1461', '-0.0812', '-0.2732', '0.3918', '-0.1345', '-0.1366', '0.07104', '-0.01189', '-0.2903', '-0.2286', '-0.014305', '0.0832', '0.2114', '-0.2554', '0.1084', '0.1671', '0.1334', '0.305', '0.0866', '0.0498', '-0.03543', '-0.247', '0.01026', '0.03314', '0.1461', '-0.001865', '0.01309', '0.04413', '0.2659', '0.1919', '0.01486', '-0.1615', '0.2097', '-0.11505', '0.0316', '-0.1519', '-0.3398', '0.05368', '0.3203', '0.0738', '-0.1871', '-0.1259', '-0.1267', '0.1232', '-0.05615', '-0.1415', '0.386', '0.0678', '0.1761', '-0.0509', '0.103', '0.3152', '0.1891', '0.005714', '0.1924', '-0.2583', '0.1769', '0.1691', '0.188', '0.1484', '-0.2106', '0.2362', '0.4717']",C35092,0003888,D001289,314.9,,,
mondo:0005303,drug dependence,['chemical dependence'],9974,,,,,C3894,0003890,,304.90,,,
mondo:0005304,biliary tract neoplasm,"['biliary tree tumor', 'tumour of the extrahepatic bile duct', 'neoplasm of biliary tree', 'biliary tree neoplasm (disease)', 'tumor of biliary tree', 'biliary tract neoplasm (disease)', 'neoplasm of extrahepatic bile ducts', 'biliary tree tumour', 'tumour of biliary tree', 'biliary tract neoplasm']",0050625,,,,,,0003891,,,,,0100574
mondo:0005306,ankylosing spondylitis,"['ankylosing spondylarthritis', 'Bekhterev syndrome', 'Bekhterev^s disease', 'Marie-Strumpell disease']",7147,,825,,,C84564,0003898,D013167,720.0,M45,,
mondo:0005308,ciliopathy,['ciliopathies'],0060340,,363250,CN580792,"['-0.313', '0.09265', '0.06903', '-0.09985', '0.04398', '-0.10736', '-0.00529', '0.05643', '-0.0805', '-0.02512', '-0.1492', '-0.1781', '-0.0871', '-0.07965', '-0.03864', '-0.1209', '0.1292', '-0.0521', '-0.1244', '-0.3843', '0.02322', '-0.1857', '0.3013', '-0.058', '0.1075', '-0.0003197', '-0.03867', '-0.02643', '-0.0679', '-0.1477', '0.2029', '0.07526', '0.116', '0.09125', '0.1381', '-0.1272', '0.003717', '-0.0096', '0.01746', '-0.2861', '0.01634', '-0.1246', '0.076', '-0.1121', '-0.05215', '-0.3389', '0.04996', '0.01947', '0.02573', '0.07886', '0.03183', '-0.02707', '-0.03513', '0.01363', '-0.2603', '-0.124', '0.2406', '-0.01796', '-0.2546', '4.84e-05', '0.1968', '0.07477', '0.03677', '0.0712', '-0.08527', '-0.03656', '0.2455', '0.1648', '-0.2283', '0.07056', '-0.193', '0.0303', '0.0562', '-0.0642', '-0.0609', '-0.0209', '-0.02315', '0.1115', '-0.2069', '-0.2336', '0.001169', '0.01956', '0.00939', '0.2517', '-0.157', '-0.1425', '-0.02531', '0.1827', '-0.0482', '-0.008286', '0.0842', '0.1757', '-0.03072', '0.0429', '0.282', '0.013214', '0.2676', '-0.269', '-0.1608', '0.1825']",,0003900,,,,,
mondo:0005309,spinal fracture,"['bone fracture of vertebral column', 'vertebral column bone fracture']",,,,,,,0003902,D016103,,,,
mondo:0005310,atrial flutter,"['atrial flutter (disease)', 'atrial flutter']",,,,,,C51224,0003911,D001282,427.32,,,0004749
mondo:0005311,atherosclerosis,['atherosclerotic cardiovascular disease'],1936,,,,,C35771,0003914,D050197,440.8,I70,,
mondo:0005312,pouchitis,,,,217067,C0376620,,,0003921,D019449,569.71,K91.850,,
mondo:0005313,necrotizing enterocolitis,"['NEC', 'necrotizing enterocolitis', 'necrotizing enterocolitis in fetus or newborn', 'necrotizing enterocolitis in foetus or newborn']",,,391673,C4082937,,C84915,0003928,D020345,777.5,,,
mondo:0005314,relapsing-remitting multiple sclerosis,"['RRMS', 'Relapsing-remitting MS']",2378,,,C0751967,,C165675,0003929,D020529,,,,
mondo:0005315,bone fracture,"['fracture of bone', 'fracture(s)', 'fracture']",,,,,,C3046,0003931,D050723,,,,
mondo:0005316,bacterial vaginosis,['BV'],3385,,,C0085166,,C116973,0003932,D016585,,,,
mondo:0005318,canker sore,"['aphthous stomatitis', 'aphthous ulcer', 'canker sore']",,,,,,C62546,0003938,D013281,,,,0032154
mondo:0005319,humerus fracture,"['fracture, humeral', 'humeral fracture', 'fractures, humeral']",,,,,,,0003943,D006810,,,,
mondo:0005320,tibia fracture,"['tibia bone fracture', 'bone fracture of tibia']",,,,,,,0003944,D013978,,,,
mondo:0005321,Fuchs^ endothelial dystrophy,"['Fuchs^ corneal dystrophy', 'FCED', 'late hereditary endothelial dystrophy', 'Fuchs^ endothelial corneal dystrophy', 'Fuchs endothelial dystrophy', 'FECD', 'Endoepithelial corneal dystrophy', 'corneal dystrophy, Fuchs endothelial', 'Fuchs endothelial corneal dystrophy']",11555,,98974,CN207231,"['-0.6978', '-0.3018', '-0.3936', '0.717', '-0.0657', '-0.4336', '0.179', '0.52', '-0.4', '-0.1556', '0.01273', '0.2603', '-0.3643', '0.2788', '-0.2744', '-0.2712', '0.3196', '-0.537', '0.328', '-1.254', '-0.5176', '-0.1613', '0.2125', '0.7993', '-0.5586', '0.213', '-0.7046', '0.4543', '0.0626', '-0.0389', '0.7275', '-0.10474', '0.07043', '0.3354', '0.07117', '0.4224', '-0.2893', '-0.3628', '0.419', '0.0467', '0.562', '-0.2917', '-0.3845', '0.0507', '0.1562', '0.861', '-0.2075', '-0.4656', '0.2349', '0.4065', '0.5767', '0.2617', '1.086', '-0.825', '-0.03726', '0.1985', '-0.2747', '-0.3335', '-0.8003', '-0.5215', '-0.1088', '-0.2876', '-0.1499', '0.3516', '0.3972', '0.253', '0.742', '0.7656', '-0.1812', '0.89', '0.4324', '-0.2593', '0.4197', '-0.056', '0.7144', '0.3047', '0.1669', '0.2788', '0.259', '-0.0808', '0.3267', '-0.2406', '-0.3943', '0.5225', '0.5', '-0.7925', '-0.03503', '0.119', '0.4302', '-0.04718', '-0.195', '0.4753', '-0.251', '-0.0916', '0.278', '-0.04123', '0.3662', '-0.4712', '-0.3628', '0.001542']",C84721,0003946,D005642,,,,
mondo:0005322,ulna fracture,"['ulna bone fracture', 'bone fracture of ulna']",,,,,,,0003950,D014458,,,,
mondo:0005323,bacterial sexually transmitted disease,,,,,C0036917,,,0003955,D015231,,,,
mondo:0005324,seasonal allergic rhinitis,"['seasonal allergic rhinitis', 'hay fever']",,,,,,C92188,0003956,D006255,,,,
mondo:0005325,radius fracture,,,,,,,,0003957,D011885,,,,
mondo:0005326,sunburn,,,,,,,,0003958,D013471,692.71,L55,,
mondo:0005327,hip fracture,,,,,,,,0003964,D006620,,,,
mondo:0005328,eye disorder,"['globe disease', 'eyeball of camera-type eye disease or disorder', 'disease of eye', 'eye disease', 'eyeball of camera-type eye disease', 'disorder of eyeball of camera-type eye', 'disease of eyeball of camera-type eye', 'eye disorder', 'disorder of eye']",5614,,,C0015397,,C26767,0003966,D005128,379.90,,,
mondo:0005333,hyperthyroxinemia,,2855,,,C0020551,"['-0.2524', '0.1302', '-0.03876', '0.04468', '0.010315', '-0.00635', '-0.0977', '0.2318', '-0.1434', '-0.02675', '-0.03485', '-0.0348', '0.03125', '0.1708', '-0.0649', '-0.1037', '-0.04822', '0.0568', '-0.08624', '-0.2544', '0.04932', '-0.1299', '0.11945', '0.013214', '0.1567', '-0.0516', '-0.01588', '-0.01918', '-0.0868', '-0.04932', '0.2206', '-0.013466', '0.1054', '0.0904', '-0.1023', '0.01875', '0.0583', '0.0779', '0.1357', '-0.2886', '0.03485', '-0.0751', '0.149', '-0.1674', '-0.0203', '-0.1418', '0.0902', '0.1284', '0.10925', '0.0398', '-0.0347', '-0.03308', '0.162', '0.02873', '-0.111', '0.1451', '0.1792', '-0.136', '-0.2544', '0.1022', '0.05032', '0.1772', '0.02567', '-0.0768', '-0.08044', '-0.05386', '0.10785', '0.1658', '-0.3105', '0.09296', '-0.10583', '0.1508', '0.02992', '-0.1142', '0.0356', '0.1228', '0.0467', '0.0667', '-0.05756', '-0.0966', '-0.012695', '0.011955', '-0.0642', '0.02534', '0.003271', '0.1124', '0.02672', '0.06152', '0.229', '0.0539', '0.05505', '0.1936', '-0.09625', '-0.0803', '0.4045', '0.1471', '0.0581', '-0.2133', '-0.2815', '0.08386']",,0004127,D006981,,,,
mondo:0005334,hereditary nephritis,"['familial nephritis', 'nephritis, familial', 'hereditary nephritis']",,,,,,,0004128,D009394,,,,
mondo:0005335,colorectal neoplasm,"['tumor of large bowel', 'tumor of colorectum', 'colorectal tumor', 'colorectum tumour', 'large bowel tumor', 'large intestine tumour', 'tumor of the large bowel', 'large intestinal neoplasm', 'colorectal neoplasm', 'colorectum neoplasm (disease)', 'large bowel neoplasm', 'large bowel tumour', 'neoplasm of the large bowel', 'colorectal tumour', 'neoplasm of colorectum', 'large intestine tumor', 'tumour of colorectum', 'large intestine neoplasm', 'tumour of the large bowel', 'tumour of large bowel', 'colorectum tumor', 'neoplasm of large bowel']",,,,,"['0.04984', '0.0933', '-0.02423', '-0.474', '0.01839', '-0.0823', '0.2322', '0.02458', '-0.0402', '0.07404', '0.002632', '0.269', '-0.1117', '0.122', '-0.2269', '-0.05707', '-0.001683', '-0.1989', '0.12244', '-0.3992', '-0.2107', '-0.3706', '0.3533', '-0.2317', '0.134', '-0.259', '0.0692', '-0.178', '-0.1304', '-0.3284', '0.4092', '-0.1004', '0.3657', '-0.0818', '0.1101', '-0.0341', '-0.4048', '0.05316', '-0.006363', '-0.1342', '-0.01735', '-0.2507', '0.10626', '-0.1252', '0.2454', '-0.1295', '-0.0549', '0.1857', '0.1873', '0.1274', '0.05286', '0.069', '-0.10455', '0.11847', '-0.43', '-0.1015', '0.00805', '0.0282', '-0.3054', '-0.0787', '0.5205', '0.02002', '-0.10876', '0.03885', '0.00646', '0.07355', '0.4976', '0.4219', '-0.1373', '0.2778', '-0.0891', '0.009476', '0.2013', '-0.04922', '0.1565', '0.01351', '-0.1511', '0.1231', '-0.00527', '-0.453', '-0.2437', '0.2617', '-0.1718', '-0.08435', '-0.4722', '-0.3154', '0.2334', '-0.1342', '0.215', '-0.2878', '0.03522', '0.1058', '-0.029', '-0.0441', '0.5034', '-0.1348', '0.303', '-0.233', '-0.2798', '0.1309']",C2956,0004142,D015179,,,,
mondo:0005336,myopathy,,423,,,C0026848,"['-0.2546', '-0.03845', '-0.0715', '-0.09766', '-0.2874', '-0.03232', '0.2615', '0.1665', '-0.2098', '-0.2429', '-0.05096', '-0.02538', '-0.0325', '0.326', '-0.09235', '-2.59e-05', '-0.492', '-0.172', '-0.1268', '-0.5283', '0.4595', '-0.408', '0.1355', '0.3496', '-0.03604', '-0.11914', '0.2412', '-0.3499', '-0.1997', '-0.1655', '0.00784', '0.1711', '0.367', '0.0856', '0.03857', '-0.0862', '-0.04538', '0.006035', '0.1385', '-0.2465', '-0.1665', '-0.4573', '-0.07916', '0.1637', '0.1791', '0.010704', '0.07025', '-0.02559', '0.3018', '0.4463', '-0.06146', '-0.0788', '0.2206', '-0.05817', '-0.12305', '-0.2896', '0.684', '-0.11584', '-0.136', '0.05447', '0.02104', '0.05258', '0.0693', '-0.2083', '-0.2122', '-0.07184', '0.1229', '0.4204', '-0.2583', '0.09314', '-0.2861', '-0.03177', '0.1929', '-0.08246', '0.247', '0.258', '0.1849', '0.4263', '-0.07776', '0.0642', '0.2695', '0.1032', '0.111', '0.01155', '-0.1109', '-0.02069', '0.2462', '0.3198', '0.3086', '0.11206', '0.2335', '-0.1326', '0.01423', '-0.037', '0.2605', '0.2354', '0.2832', '-0.1855', '-0.4133', '0.2219']",C101216,0004145,,728.3,,,
mondo:0005338,open-angle glaucoma,"['wide-angle glaucoma', 'POAG', 'open angle glaucoma', 'glaucoma, primary open angle', 'glaucoma simplex', 'primary open angle glaucoma', 'pigmentary glaucoma']",1067,,,C0017612,"['0.4478', '-0.2244', '-0.787', '1.016', '-0.11084', '0.0598', '0.0502', '0.905', '-0.2507', '-0.7715', '0.5312', '-0.1692', '-0.006474', '0.8423', '-0.8843', '-0.1792', '-0.084', '-0.00891', '0.1786', '-0.622', '0.1901', '0.4604', '0.03336', '-0.1202', '0.04968', '-0.301', '-0.0696', '0.754', '-0.249', '0.3274', '0.3188', '-0.2688', '0.585', '0.1188', '-0.2311', '-0.03033', '-0.1234', '-0.4312', '0.3975', '-0.4978', '0.6016', '-0.513', '0.6187', '-0.1848', '-0.3909', '0.8696', '0.2688', '-0.0845', '1.028', '-0.3762', '0.001389', '-0.043', '-0.612', '-1.462', '0.4883', '-0.2244', '0.6006', '0.547', '-1.524', '-0.6514', '-0.558', '0.0997', '0.0956', '0.6577', '-0.6772', '-0.3518', '0.3623', '0.634', '-0.3396', '0.8394', '0.1752', '0.859', '0.4495', '-0.6885', '-0.3926', '0.2244', '0.4175', '1.07', '-0.1554', '0.389', '0.2673', '-0.09235', '-0.6514', '0.8145', '0.1908', '0.07855', '0.4204', '-0.1714', '0.629', '0.622', '-0.04892', '0.10065', '-0.6924', '0.3484', '1.4375', '-0.1918', '-0.358', '-0.3123', '-0.3252', '-0.1975']",C34641,0004190,D005902,365.13,,,
mondo:0005339,androgenetic alopecia,"['androgenic alopecia', 'male pattern baldness', 'androgenetic alopecia', 'alopecia androgenetica, male pattern baldness']",0050801,,,,,,0004191,,704.09,,,
mondo:0005340,alopecia areata,"['alopecia circumscripta', 'alopecia areata', 'circumscribed alopecia']",986,,,C0002171,,,0004192,D000506,704.01,L63,,
mondo:0005341,skin basal cell carcinoma,"['skin basal cell carcinoma', 'malignant basal cell tumour', 'basal cell epithelioma', 'basal cell carcinoma of the skin', 'basal cell tumour (morphologic abnormality)', 'epithelioma basal cell', 'BCC', 'basal cell carcinoma of skin', 'basal cell carcinoma', 'basal cell cancer', 'basal cell tumour', 'basal cell tumor', 'skin basal cell cancer', 'basal cell skin carcinoma', 'malignant basal cell tumour (morphologic abnormality)']",2513,,,C0751676,"['0.291', '0.1621', '-0.557', '0.6704', '0.2314', '-0.2532', '0.1288', '0.3828', '-0.1897', '-0.0349', '0.5327', '0.437', '-0.1248', '0.1652', '-1.066', '-0.8027', '0.529', '-0.6772', '0.272', '-0.1687', '-0.591', '-0.2607', '0.03073', '-0.5503', '0.00868', '-0.2534', '-0.7085', '-0.1757', '-0.3877', '-0.3237', '0.5454', '-0.241', '0.1022', '-0.1218', '0.4517', '0.4062', '-0.596', '-0.243', '0.3032', '-0.5425', '0.3008', '-0.4177', '-0.05222', '0.3645', '0.18', '-0.4492', '-0.001042', '-0.6636', '0.45', '-0.4304', '0.6313', '-0.6016', '0.2047', '-0.01599', '-0.677', '-0.243', '0.1031', '0.4883', '-0.4485', '-0.1515', '-0.06604', '0.03207', '-1.035', '0.2988', '-0.1206', '0.755', '0.671', '0.78', '0.02116', '1.332', '0.2625', '0.606', '0.2081', '-0.01901', '0.2194', '0.6035', '-1.077', '-0.0881', '0.05408', '-0.646', '-0.2878', '0.05954', '-0.0848', '-0.3315', '-0.2175', '-0.8223', '0.1921', '0.4072', '0.3928', '0.2174', '0.63', '-0.03595', '-0.371', '0.446', '0.39', '0.05637', '-0.00702', '-0.8228', '-0.251', '-0.0934']",C2921,0004193,,,,,0002671
mondo:0005342,IgA glomerulonephritis,"['IgA nephropathy', 'IgA glomerulonephritis', 'primary IgA nephropathy', 'segmental glomerulonephritis', 'focal glomerulonephritis', 'berger^s disease', 'berger^s IgA or IgG nephropathy']",2986,,34145,C0017661,"['0.8213', '0.3074', '-0.545', '0.346', '-0.05243', '-0.4595', '0.05164', '-0.06604', '-0.6143', '-0.02158', '0.1987', '-0.01785', '-0.497', '1.14', '-0.2244', '-0.311', '-0.1809', '0.538', '0.709', '-0.0444', '-0.1655', '-1.082', '0.8057', '-0.03253', '0.807', '-0.245', '-0.7856', '0.874', '0.203', '-0.202', '0.09625', '0.4084', '0.7617', '0.06433', '-0.1653', '-0.1562', '-0.384', '0.7817', '0.4124', '-0.534', '-0.452', '-0.129', '0.07635', '-0.4785', '0.2585', '-0.5205', '-0.5566', '-0.229', '-0.1139', '-0.03912', '0.2952', '0.07324', '1.261', '-0.406', '-0.563', '-0.1471', '0.0366', '0.04922', '-0.759', '-0.4773', '-0.7305', '0.2656', '-0.1729', '-0.2191', '-0.3037', '-0.3752', '0.267', '0.4216', '-0.9673', '0.584', '-0.8467', '0.2854', '0.3718', '-0.2214', '0.00665', '0.2327', '0.662', '1.029', '-0.05722', '0.4263', '-0.3552', '0.1394', '0.0005894', '0.2659', '0.2399', '-0.1203', '0.12085', '-0.3184', '0.00956', '1.162', '0.723', '0.3174', '-0.5234', '0.1825', '0.7427', '0.7383', '-0.3694', '-0.7983', '-0.7812', '0.07104']",C34643,0004194,D005922,583.9,,,
mondo:0005344,hepatitis B virus infection,"['chronic hepatitis B', 'Hepatitis B infection', 'viral Hepatitis B', 'hepatitis type B', 'Hepatitis B', 'hepatitis B infection', 'serum hepatitis', 'Hepatitis B virus caused hepatitis']",2043,,,C0019163,,C3097,0004197,D006509,070.30,,,
mondo:0005345,hypospadias,"['familial hypospadias', 'hypospadias', 'hypospadias (disease)', 'hypospadias familial']",10892,,440,CN205090,"['-0.495', '-0.009094', '0.04056', '-0.336', '-0.1833', '-0.4531', '-0.03693', '1.198', '-0.776', '-0.4412', '0.3967', '-0.2078', '-0.5674', '0.081', '0.1246', '0.05692', '-0.2341', '-0.1107', '-0.5444', '-0.643', '-0.709', '0.3513', '0.2793', '-0.55', '0.1649', '-0.0304', '-0.3572', '0.3606', '0.288', '-0.3733', '0.2585', '-0.7476', '0.04648', '-0.0765', '0.6885', '0.1937', '0.2732', '-0.4666', '0.265', '-0.443', '0.92', '1.114', '0.01092', '-0.2036', '0.6274', '-0.8496', '0.8267', '-0.2659', '0.4072', '0.5596', '-0.1451', '-0.5845', '-0.463', '0.1075', '-0.3142', '0.971', '0.2493', '0.143', '-0.244', '0.1018', '0.08295', '0.1339', '-0.2181', '0.5166', '0.1212', '0.553', '0.7007', '0.3145', '-0.6553', '1.052', '0.1126', '0.867', '0.446', '-0.2198', '-0.1962', '0.6025', '0.423', '0.8477', '-0.03494', '-0.6177', '0.351', '0.304', '-0.1101', '-0.6177', '0.1641', '-0.03116', '0.04404', '-0.532', '0.5127', '0.0141', '-0.4692', '-0.2229', '-0.0956', '0.3123', '0.5186', '-0.5703', '0.2703', '-0.3872', '-0.2925', '-0.1622']",C40341,0004209,D007021,752.61,,,0000047
mondo:0005346,gallstones,,,,,,,,0004210,D042882,574.20,,,
mondo:0005347,hypertriglyceridemia,"['hypertriglyceridemia', 'hypertriglyceridemia (disease)']",,,,C0020557,,,0004211,D015228,,,,0002155
mondo:0005348,keloid,,,,,,,C3145,0004212,D007627,701.4,,,
mondo:0005349,otosclerosis,"['otosclerosis (disease)', 'otosclerosis']",12185,,2794,C0029899,,C185242,0004213,D010040,387.9,,,0000362
mondo:0005350,abdominal aortic aneurysm,"['aortic aneurysm, familial abdominal 1']",7693,,,C0162871,,,0004214,D017544,,,,
mondo:0005351,anorexia nervosa,,8689,,36297,,,C34387,0004215,D000856,307.1,F50.0,,
mondo:0005352,conduct disorder,,12995,,,,,C89329,0004216,D019955,312.9,,,
mondo:0005354,chronic hepatitis C virus infection,"['hepatitis C infection, chronic', 'chronic Hepatitis C', 'hepatitis C, chronic']",,,,,,,0004220,D019698,070.44,,,
mondo:0005355,coronary restenosis,,4247,,,C0948480,,,0004224,D023903,,,,
mondo:0005356,coronary vasospasm,"['coronary artery vasospasm', 'coronary artery spasm', 'coronary vasospasm']",11840,,,C0010073,,,0004225,D003329,413.9,,,
mondo:0005357,Creutzfeldt Jacob disease,"['Jakob-Creutzfeldt disease', 'CJD', 'CJD (Creutzfeldt Jakob disease)', 'transmissible virus dementia', 'Subacute spongiform encephalopathy', 'Creutzfeldt-Jakob disease', 'Creutzfeldt Jacob syndrome', 'Creutzfeldt-Jacob disease', 'classic Creutzfeldt-Jakob disease', 'Creutzfeldt Jakob disease']",11949,,,,,C26802,0004226,D007562,046.19,,,
mondo:0005358,Dengue hemorrhagic fever,"['Dengue haemorrhagic fever', 'DHF']",12206,,,,,C34683,0004227,,,A91,,
mondo:0005359,drug-induced liver injury,"['drug induced hepatotoxicity', 'drug-induced disorder of liver']",,,,,,,0004228,D056486,,,,
mondo:0005361,eosinophilic esophagitis,['EoE'],13922,,73247,C0341106,,C27105,0004232,D057765,530.13,K20.0,10064212,
mondo:0005362,erectile dysfunction,"['sexual impotence, Male', 'impotence, male sexual', 'male sexual impotence', 'male impotence', 'erectile dysfunction', 'erectile dysfunction (disease)', 'sexual impotence (finding)', 'impotence, male', 'dysfunction, erectile', 'male erectile Disorder', 'impotence', 'sexual impotence']",1875,,,,,C34801,0004234,D007172,,,,0000802
mondo:0005363,inherited focal segmental glomerulosclerosis,,,,,,"['0.0536', '-0.00912', '-0.1351', '-0.2588', '-0.2976', '-0.2715', '0.2128', '-0.2333', '0.01062', '-0.2703', '0.0739', '-0.1207', '-0.3318', '-0.0355', '-0.3044', '-0.2228', '-0.2458', '-0.301', '0.0963', '-0.529', '0.3535', '-0.297', '0.1372', '0.07605', '0.2483', '-0.4084', '0.07434', '0.06082', '-0.06915', '-0.1389', '0.2869', '-0.1619', '0.3464', '-0.1183', '0.3896', '-0.1492', '-0.0747', '-0.11005', '0.1265', '-0.367', '-0.445', '0.03418', '0.1465', '0.04935', '0.1346', '-0.2452', '0.1135', '-0.0723', '0.3657', '-0.00572', '-0.05127', '0.2384', '0.613', '-0.05853', '0.3381', '-0.2141', '0.478', '-0.02237', '-0.769', '-0.00757', '-0.1981', '-0.1605', '0.11884', '-0.3887', '-0.05975', '0.1038', '0.4243', '0.2554', '-0.2507', '0.4834', '-0.323', '-0.3308', '0.2517', '0.3108', '-0.0758', '0.232', '0.2507', '0.423', '-0.1525', '-0.02153', '-0.4258', '0.38', '0.0941', '0.04492', '-0.0887', '-0.3938', '0.1884', '-0.0254', '0.276', '0.5806', '0.0409', '-0.12335', '-0.2168', '-0.12054', '0.479', '0.2812', '0.3345', '-0.09424', '-0.05307', '0.11']",,0004236,,,,,
mondo:0005364,Graves disease,"['Graves^ hyperthyroidism', 'exophthalmic goiter', 'Graves disease', 'grave^s disease', 'Basedow^s disease', 'Graves^ disease', 'Basedow disease', 'exophthalmic goitre', 'parry disease']",12361,,,,,C3071,0004237,D006111,242.0,,,
mondo:0005365,hearing loss disorder,"['deafness', 'loss of hearing', 'loss, hearing', 'hearing impairment', 'hearing loss', 'hypoacusis', 'hypoacuses']",,,,C1384666,,C35731,0004238,D034381,389.9,H90,,
mondo:0005366,chronic hepatitis B virus infection,"['hepatitis B infection, chronic', 'chronic Hepatitis B', 'hepatitis B, chronic']",,,,C0524909,,,0004239,D019694,,,,
mondo:0005367,heroin dependence,['Heroin addiction'],9976,,,CN236651,,C34694,0004240,D006556,,,,
mondo:0005369,carcinoid tumor,"['carcinoid', 'neuroendocrine neoplasm G1', 'neuroendocrine tumor G1', 'NET G1', 'neuroendocrine tumour G1', 'carcinoid tumor', 'carcinoid tumour (disease)', 'carcinoid tumor (disease)']",,,,,,C2915,0004243,D002276,209.60,,,0100570
mondo:0005371,mood disorder,,3324,,,CN236678,,C92200,0004247,D019964,296.99,F30-F39,,
mondo:0005372,male infertility,"['male reproductive system infertility disorder', 'infertility disorder of male reproductive system', 'male reproductive system infertility']",12336,,,C0021364,,,0004248,D007248,606.9,N46,,
mondo:0005373,meningococcal infection,"['meningococcal disease', 'infections, Neisseria meningitidis', 'Neisseria meningitidis infection']",,,,C0025303,,,0004249,D008589,036.9,A39,,
mondo:0005374,bone marrow neoplasm,"['bone marrow tumor', 'bone marrow cancer', 'malignant bone marrow tumour', 'neoplasm of bone marrow', 'tumor of bone marrow', 'tumour of bone marrow', 'bone marrow neoplasm (disease)', 'bone marrow neoplasm', 'bone marrow tumour', 'malignant bone marrow tumor']",4960,,,C0282609,,C35370,,D019046,238.79,,,
mondo:0005375,nasopharyngeal neoplasm,"['nasopharynx tumor', 'neoplasm of the nasopharynx', 'nasopharynx tumour', 'tumour of nasopharynx', 'tumor of the nasopharynx', 'nasopharyngeal tumour', 'tumour of the nasopharynx', 'nasopharynx neoplasm (disease)', 'tumor of nasopharynx', 'nasopharyngeal neoplasms', 'nasopharyngeal tumor', 'neoplasm of nasopharynx']",,,,C0027439,"['-0.115', '0.1038', '-0.04916', '-0.3127', '0.01886', '-0.0774', '0.2795', '0.04373', '-0.04727', '0.02422', '0.008', '0.07355', '-0.136', '0.1018', '-0.3477', '-0.0716', '-0.0306', '-0.2354', '0.1208', '-0.325', '-0.2124', '-0.3354', '0.286', '-0.1843', '0.1732', '-0.0889', '0.08417', '-0.1873', '-0.1608', '-0.2737', '0.352', '0.0881', '0.4275', '-0.0716', '0.05484', '0.04773', '-0.2522', '-0.079', '-0.04752', '-0.3145', '-0.1859', '-0.3486', '0.0986', '-0.1594', '0.1606', '-0.1813', '0.03238', '0.04938', '0.1575', '0.09045', '0.10034', '0.0909', '-0.01595', '0.1738', '-0.3313', '-0.04807', '0.0971', '0.10614', '-0.351', '-0.1191', '0.2856', '0.0387', '-0.2236', '0.1111', '0.0601', '0.108', '0.46', '0.4053', '-0.2089', '0.3088', '-0.1655', '0.02296', '0.1141', '-0.01518', '0.1758', '0.04855', '-0.08936', '0.00835', '0.03598', '-0.3608', '-0.3257', '0.1985', '-0.2062', '-0.01309', '-0.2128', '-0.2556', '0.2101', '-0.04712', '0.3127', '-0.2458', '0.014366', '0.1298', '0.1015', '-0.06183', '0.4026', '-0.09076', '0.361', '-0.2147', '-0.2301', '0.06024']",C3257,0004252,D009303,,,,
mondo:0005376,membranous glomerulonephritis,"['membranous Glomerulonephropathy', 'membranous nephropathy']",10976,,,C0017665,,C34645,0004254,D015433,583.1,,,
mondo:0005377,nephrotic syndrome,"['syndrome, nephrotic', 'syndromes, nephrotic', 'nephrosis', 'nephrotic syndromes', 'nephrotic syndrome']",1184,,564127,C0027726,"['0.518', '-0.2798', '0.1681', '-0.006516', '-0.4397', '-0.1282', '0.2817', '0.1803', '-0.5996', '-0.3208', '0.272', '-0.1683', '-0.559', '0.891', '-0.3628', '-0.2023', '0.03458', '0.6045', '0.858', '-0.563', '0.696', '-0.9707', '0.4734', '0.5566', '0.09045', '-0.592', '-0.5645', '0.2534', '0.05392', '-0.35', '0.8364', '-0.1659', '0.8877', '-0.01509', '-0.6006', '-0.176', '-0.12244', '0.0992', '0.2751', '-0.5312', '-0.4314', '0.02368', '-0.4412', '-0.548', '0.0986', '-0.2917', '-0.11755', '-0.1515', '0.2224', '-0.2776', '-0.1891', '0.5776', '0.9937', '-0.717', '-0.1826', '-0.4976', '0.0639', '-0.05872', '-1.0625', '-0.1644', '-0.2551', '-0.338', '-0.03647', '-0.6567', '-0.1079', '-0.1472', '0.5767', '0.00878', '-0.794', '0.4578', '-0.523', '0.528', '0.5767', '-0.1781', '0.2395', '0.11804', '0.3186', '0.783', '-0.2441', '0.3813', '-0.256', '-0.2449', '-0.2418', '-0.1658', '0.00605', '-0.4302', '-0.004482', '-0.2886', '0.5825', '0.3223', '0.468', '0.753', '-0.9126', '-0.1296', '0.3774', '0.7227', '-0.415', '-0.753', '-0.2008', '-0.277']",C34845,0004255,D009404,581.9,,,
mondo:0005379,neurotic disorder,"['disorder, neurotic', 'neuroses', 'neurotic depressive state', 'psychoneurosis NOS', 'Psychoneuroses', 'reactive depression', 'neurotic disorder', 'depressive neurosis', 'psychoneurosis', 'neurotic depression', 'disorders, neurotic', 'neurotic depression reactive type', 'neurosis']",4964,,,,,C35369,0004257,D009497,300.9,F34.1,,
mondo:0005380,osteonecrosis,"['bone necrosis', 'ischemic bone disease', 'aseptic necrosis', 'ischaemic bone disease', 'osteonecrosis']",10159,,399158,,,C35476,0004259,D010020,733.49,M87,,
mondo:0005381,bone disorder,"['skeletal disease', 'disorder of bone element', 'bone element disease or disorder', 'bone element disease', 'disease of bone element', 'rare bone disease related to a common gene or pathway defect']",0080001,,364803,CN204768,,,0004260,D001847,733.99,M80-M85,,
mondo:0005382,bone Paget disease,"['bone Paget^s disease', 'Paget^s bone disease', 'osseous Paget^s disease', 'Pagets disease (bone)', 'Paget^s disease of bone', 'Paget^s disease of the bone', 'Paget^s disease', 'bone Paget disease', 'Paget disease of bone', 'familial Paget^s disease of bone', 'osteitis deformans']",5408,,280110,C0029401,"['-0.243', '0.1189', '0.1467', '-0.1151', '0.0653', '-0.1576', '0.06445', '0.3716', '-0.1761', '-0.05283', '-0.1252', '-0.05103', '0.2837', '0.1405', '-0.07135', '-0.11926', '-0.002125', '-0.2161', '0.137', '-0.4583', '0.11304', '-0.1309', '0.508', '-0.2158', '0.0661', '-0.171', '0.0638', '-0.2352', '-0.3965', '-0.12463', '0.1593', '0.1738', '0.0967', '0.2393', '0.1405', '0.05548', '0.2145', '0.1941', '-0.06006', '-0.53', '0.1973', '-0.11884', '0.3545', '-0.2249', '-0.01596', '-0.3782', '-0.0912', '0.1556', '0.3467', '-0.06104', '0.137', '-0.2245', '0.4324', '0.529', '-0.08026', '-0.3271', '0.05893', '-0.1692', '-0.2324', '-0.14', '0.4712', '0.1771', '-0.3389', '-0.4507', '0.1444', '-0.1536', '0.2627', '0.1708', '-0.1764', '0.2081', '-0.02141', '-0.04907', '0.1139', '-0.1392', '0.2223', '-0.1554', '-0.2164', '0.167', '-0.1405', '-0.4517', '-0.1821', '-0.1489', '-0.0955', '0.11554', '-0.4568', '-0.01671', '0.2216', '-0.0207', '0.3188', '-0.1647', '0.02391', '-0.1213', '-0.5093', '0.1967', '0.1897', '0.10046', '0.04953', '-0.4578', '-0.2115', '-0.14']",C3292,0004261,,,,,
mondo:0005383,panic disorder,['panic anxiety syndrome'],594,,,CN240645,,C34890,0004262,D016584,300.01,,,
mondo:0005384,focal epilepsy,"['localisation-related epilepsy', 'partial epilepsy', 'focal epilepsy']",2234,,,C0014547,,C122812,0004263,D004828,345.50,,,
mondo:0005385,vascular disorder,"['vascular disorder', 'disorder of vasculature', 'vasculopathy', 'disease of vasculature', 'vasculature disease', 'vascular tissue disease', 'vasculature disease or disorder']",178,,,C0042373,,C35117,0004264,D014652,442.9,I70-I79,,
mondo:0005386,peripheral arterial disease,"['peripheral artery disease', 'pad', 'peripheral arterial disorder']",0050830,,,,,C84496,0004265,D058729,443.81,,,
mondo:0005387,primary ovarian failure,"['primary ovarian insufficiency', 'hypergonadotropic hypogonadism (female)', 'premature menopause', 'primary ovarian failure', 'premature ovarian insufficiency', 'hypergonadotropic hypogonadism', 'premature ovarian failure']",5426,,619,C0085215,"['-0.384', '-0.4373', '-0.1448', '0.0796', '0.1378', '-0.2347', '0.3337', '0.0851', '-0.1212', '-0.2075', '0.273', '0.548', '-0.361', '0.9272', '-0.013535', '-0.5835', '-0.11426', '0.659', '-0.6606', '-0.517', '0.2825', '-0.151', '-0.1732', '-0.3079', '-0.04706', '-0.02643', '0.3062', '0.0877', '0.1771', '-0.1533', '1.01', '0.6733', '0.1869', '-0.5244', '0.0922', '-0.11896', '-0.2185', '0.266', '0.2334', '-0.2373', '0.7466', '0.3887', '0.2996', '-0.2328', '0.01046', '-0.808', '-0.00971', '-0.3628', '0.2435', '0.6475', '0.5566', '-0.3093', '-0.03165', '0.3042', '-0.2668', '0.01051', '-0.3152', '-0.324', '-0.4714', '-0.3594', '0.2532', '0.3635', '-0.0721', '0.1284', '-0.2664', '0.2175', '0.1776', '0.732', '-0.852', '0.5195', '0.1092', '-0.157', '0.1234', '-0.7627', '0.329', '0.4072', '-0.04974', '0.5347', '0.3445', '-0.1351', '0.00966', '0.3567', '0.09906', '-0.0587', '0.0769', '-0.3074', '0.4548', '0.04855', '0.8896', '0.0874', '-0.588', '0.4795', '-0.403', '0.3997', '0.1218', '-0.3225', '-0.07654', '-0.4302', '-0.267', '0.1462']",C113352,0004266,D016649,256.39,E28.3,,
mondo:0005388,primary biliary cholangitis,"['cholestatic cirrhosis', 'familial primary biliary cirrhosis', 'biliary cirrhosis, primary', 'primary biliary cirrhosis', 'PBC', 'chronic nonsuppurative destructive cholangitis', 'primary Bilary cirrhosis (PBC)', 'chronic non-suppurative destructive cholangitis', 'Hanot syndrome', 'biliary liver cirrhosis']",12236,,186,C0008312,,C27167,0004267,D008105,571.6,,10019137,
mondo:0005391,restless legs syndrome,"['RLS', 'WED', 'restless leg syndrome', 'Wittmaack-Ekbom syndrome', 'Willis-Ekbom disease']",0050425,,,C0035258,"['-0.1538', '0.2186', '-0.5376', '-0.2065', '-0.02623', '-0.2974', '0.2285', '0.4666', '-0.3765', '-0.0908', '0.7236', '0.3938', '-0.09186', '0.8936', '-0.0385', '-0.509', '0.0178', '-0.174', '-0.11786', '-1.172', '-0.636', '-0.1803', '-0.4856', '-0.10657', '-0.1587', '-0.3381', '0.0638', '-0.00986', '-0.2339', '0.288', '-0.2603', '-0.6904', '0.0831', '-0.006245', '-0.1104', '-0.0172', '-0.425', '-0.5605', '0.2832', '-0.10724', '0.04874', '-0.02776', '0.09955', '0.3818', '0.4373', '-0.2163', '0.02974', '0.1841', '0.1763', '0.899', '-0.012405', '-0.0989', '0.1202', '0.2979', '0.09735', '-0.3628', '-0.142', '0.4968', '0.13', '-0.454', '0.1853', '0.3113', '0.1583', '-0.04086', '-0.7554', '0.535', '0.2382', '0.696', '-0.2053', '0.5996', '-0.5854', '0.001041', '-0.09827', '-0.664', '-0.1602', '0.266', '0.1735', '1.02', '0.294', '0.1942', '-0.0474', '-0.2927', '0.4167', '-0.04312', '0.7563', '0.1299', '0.03152', '-0.05774', '0.5366', '0.1621', '0.03818', '-0.3655', '-0.5005', '0.05005', '0.6704', '0.2063', '-0.488', '-0.3726', '-0.2216', '0.1401']",C84501,0004270,D012148,333.99,G25.81,,
mondo:0005392,scoliosis,,0060249,,,,,C78603,0004273,D012600,737.43,M41,,0002650
mondo:0005393,gout,"['articular gout', 'tophaceous disease', 'gout', 'tophaceous gout', 'gouty arthropathy', 'chronic gout', 'gouty arthritis']",13189,,,C0018099,,C34650,0004274,D006073,274.9,M10,,
mondo:0005394,brain infarction,,3454,,,C0751955,,,0004277,D020520,,,,
mondo:0005395,movement disorder,"['movement disorders', 'movement disease']",480,,,,,C116757,0004280,D009069,333.99,,,
mondo:0005396,thoracic aortic aneurysm,,14004,,91387,C0162872,"['0.1975', '-0.1543', '-0.616', '-0.1628', '0.02722', '-0.01917', '0.07715', '0.54', '-0.4102', '-0.2598', '0.505', '-0.4954', '0.5234', '0.6426', '-0.749', '-0.0952', '-0.68', '0.2369', '-0.0673', '-0.6133', '0.3298', '0.10675', '0.2615', '0.4167', '-0.4302', '0.0747', '0.2722', '0.589', '0.1047', '-0.0565', '0.8267', '-0.2744', '0.574', '-0.02588', '0.1396', '0.03262', '0.2207', '0.3435', '0.4062', '-1.09', '-0.0357', '0.1216', '0.28', '0.4338', '0.3489', '-0.1399', '-0.6104', '0.11774', '0.6157', '0.079', '-0.06433', '-0.11505', '0.375', '0.00908', '-0.383', '-0.7407', '-0.343', '0.1654', '-0.2123', '-0.724', '-0.2595', '0.2693', '-0.04712', '-0.6265', '0.2805', '0.667', '-0.0717', '0.3496', '-0.5244', '0.526', '-0.02739', '0.3992', '-0.2017', '-0.3022', '0.24', '0.1633', '-0.02069', '0.3076', '-0.1633', '-0.4238', '-0.709', '0.02795', '0.08765', '-0.12164', '0.6016', '-0.2776', '0.6265', '0.1882', '0.4421', '-0.5815', '-0.4497', '-0.215', '-0.00651', '0.7305', '0.3142', '-0.2776', '0.459', '-0.2217', '-0.1953', '0.1957']",,0004282,D017545,,,,
mondo:0005397,goiter,"['goiter (disease)', 'goiter', 'Thyromegaly', 'goitre (disease)']",12176,,,,,C26785,0004283,D006042,240.9,,,0000853
mondo:0005398,upper aerodigestive tract neoplasm,,,,,,,,0004284,,239.89,,,
mondo:0005399,venous thromboembolism,['venous thromboembolism'],,,,C1861172,,C99537,0004286,D054556,,,,
mondo:0005401,colonic neoplasm,"['tumour of colon', 'colonic tumour', 'colon neoplasm', 'tumor of colon', 'colon tumour', 'colon neoplasm (disease)', 'neoplasm of colon', 'tumour of the colon', 'tumor of the colon', 'neoplasm of the colon', 'colonic neoplasm', 'colon tumor', 'colonic tumor']",,,,C0009375,,C2953,0004288,D003110,,,,
mondo:0005402,lymphoid leukemia,"['lymphoid leukaemia (disease)', 'lymphocytic leukemia', 'lymphocytic leukaemia', 'lymphogenous leukaemia', 'subacute lymphoid leukaemia', 'lymphoid leukemia', 'lymphoid leukemia (disease)', 'lymphogenous leukemia', 'subacute lymphoid leukemia', 'leukemia, LYMPHOCYTIC, malignant']",10747,,,C0152271,,C7539,0004289,D007945,204.20,,,0005526
mondo:0005404,myalgic encephalomeyelitis/chronic fatigue syndrome,"['chronic fatigue syndrome', 'myalgic encephalomyelitis', 'Postviral fatigue syndrome', 'chronic fatigue immune dysfunction syndrome', 'myalgic encephalitis', 'systemic exertion intolerance disease', 'CFS']",8544,,1983,C0015674,,C3037,0004540,D015673,780.79,,,
mondo:0005405,childhood onset asthma,"['childhood asthma', 'pediatric asthma', 'paediatric asthma', 'asthma of childhood']",0080815,,,C0264408,,,0004591,,,,,
mondo:0005406,gestational diabetes,"['maternal gestational diabetes mellitus', 'gestational diabetes mellitus', 'diabetes in pregnancy', 'GDM']",11714,,,C0085207,,C34942,0004593,D016640,,,,
mondo:0005407,childhood eosinophilic esophagitis,"['paediatric eosinophilic esophagitis', 'eosinophilic esophagitis of childhood', 'pediatric eosinophilic esophagitis']",,,,,,,0004594,,,,,
mondo:0005408,diabetes mellitus type 2 associated cataract,,,,,,,,0004596,,,,,
mondo:0005411,gallbladder cancer,"['tumor of the gallbladder', 'malignant gallbladder neoplasm', 'malignant gallbladder tumor', 'malignant neoplasm of gallbladder', 'malignant gall bladder neoplasm', 'malignant tumor of the gallbladder', 'gallbladder neoplasm', 'malignant tumor of gallbladder', 'malignant tumour of gallbladder', 'localised malignant gallbladder neoplasm', 'malignant neoplasm of gall bladder', 'localized malignant gallbladder neoplasm', 'malignant tumour of the gallbladder', 'malignant neoplasm of the gallbladder', 'malignant gallbladder tumour', 'cancer of gall bladder', 'tumour of the gallbladder', 'gall bladder cancer', 'gallbladder Ca']",3121,,,C0153452,,C7481,0004606,,156.8,,,
mondo:0005412,duodenal ulcer,"['stress Ulcer', 'curling Ulcer', 'duodenal ulcer (disease)', 'curling^s ulcers']",1724,,,,,C26755,0004607,D004381,532,K26,,0002588
mondo:0005413,cystic fibrosis associated meconium ileus,['cystic fibrosis associated meconium ileum'],,,,,,,0004608,,,,,
mondo:0005414,treatment-refractory schizophrenia,"['treatment-refractory schizophrenia', 'TRS']",,,,,,,0004609,,,,,
mondo:0005416,"osteoarthritis, knee",,,,,,,,0004616,D020370,,,,
mondo:0005417,wet macular degeneration,"['Senile macular degeneration, wet', 'neovascular age-related macular degeneration', 'wet age related macular degeneration', 'wet senile macular retinal degeneration', 'wet ARMD', 'wet AMD', 'exudative senile macular degeneration of retina', 'Kuhnt-Junius degeneration']",10873,,,C2237660,,,0004683,D057135,362.52,,,
mondo:0005418,non-compaction cardiomyopathy,,,,,,,,0004686,,,,,
mondo:0005419,metamphetamine dependence,,,,,,,,0004701,,,,,
mondo:0005420,hypothyroidism,"['thyroid insufficiency', 'thyroid deficiency', 'underactive thyroid']",1459,,,,,C26800,0004705,D007037,244.9,,,
mondo:0005424,elephantiasis,,4976,,,C0013882,,,0004711,D004604,,,,
mondo:0005425,podoconiosis,"['nonfilarial elephantiasis', 'soil elephantiasis', 'non-filarial elephantiasis']",0050138,,,,,,0004712,,457.1,,,
mondo:0005426,MRI defined brain infarct,,,,,,,,0004715,,,,,
mondo:0005429,prion disease,"['prion protein disease', 'prion disease pathway', 'spongiform encephalopathy', 'prion induced disorder']",649,,,,"['-0.2988', '0.1959', '0.1235', '0.2109', '0.042', '-0.1543', '-0.04218', '-0.0647', '-0.1552', '0.1075', '-0.02452', '0.08246', '-0.01429', '-0.03915', '0.2405', '-0.2966', '-0.2047', '-0.02655', '-0.2095', '-0.2913', '0.405', '-0.2175', '0.1654', '-0.05527', '0.0744', '-0.3916', '-0.06024', '-0.004326', '-0.4563', '0.02211', '0.2117', '-0.1897', '0.04828', '-0.03104', '0.3054', '-0.04752', '-0.1445', '0.0712', '0.2017', '-0.2507', '0.0622', '-0.3994', '0.0971', '0.1903', '-0.012184', '-0.603', '-0.04196', '0.00696', '0.151', '0.2069', '0.1543', '0.2363', '0.1886', '0.0877', '-0.10315', '-0.1604', '0.3643', '0.0702', '-0.3071', '0.1373', '0.0737', '0.2161', '0.05035', '0.04907', '-0.1315', '0.0837', '0.3535', '0.3184', '-0.0841', '0.5767', '0.05978', '0.2231', '0.05896', '-0.05865', '-0.2045', '0.2131', '0.11224', '0.4465', '-0.2725', '-0.1001', '-0.275', '-0.3777', '0.11383', '0.1766', '-0.2445', '-0.2494', '-0.03986', '0.3088', '0.0506', '0.1211', '0.2725', '0.1448', '-0.1098', '0.3115', '-0.00391', '0.252', '0.09076', '-0.2383', '0.1064', '0.06125']",C128346,0004720,D017096,046.19,,,
mondo:0005430,early onset hypertension,,,,,,,,0004772,,,,,
mondo:0005432,alcohol and nicotine codependence,,,,,,,,0004776,,,,,
mondo:0005433,alcohol withdrawal,,,,,C0236663,,,0004777,,291.81,,,
mondo:0005434,skin sensitivity to sun,,,,,,,,0004795,,,,,
mondo:0005435,anti-neutrophil antibody associated vasculitis,,,,,,,,0004826,,,,,
mondo:0005436,postoperative ventricular dysfunction,,,,,,,,0004889,,,,,
mondo:0005437,testicular dysgenesis syndrome,,,,,C2919755,,,0004893,,,,,
mondo:0005438,metastatic malignant neoplasm in the lymph nodes,"['metastatic tumor to lymph node', 'metastasis to lymph node', 'metastatic neoplasm to the lymph node', 'metastatic tumour to lymph node', 'Metastases to lymph nodes', 'metastatic malignant neoplasm to the lymph nodes']",,,,C0686619,,C4904,0004906,,,,,
mondo:0005439,familial hypercholesterolemia,"['hyperbetalipoproteinemia', 'familial hyperbetalipoproteinaemia', 'hyperlipoproteinemia type II', 'type II hyperlipidemia', 'Fredrickson type IIa hyperlipoproteinemia', 'Fredrickson type IIa lipidaemia', 'familial hypercholesteremia']",13810,,477811,CN118841,"['-0.05908', '-0.0642', '-0.5093', '1.004', '0.3755', '-0.3545', '-0.1299', '0.3809', '-0.2783', '-0.379', '-0.0877', '0.4834', '0.3677', '0.2437', '-0.3574', '-0.865', '0.282', '0.4197', '-0.07446', '0.07556', '0.783', '-0.4182', '0.3833', '0.2413', '0.0959', '-0.242', '0.1099', '0.2123', '0.2385', '-0.3137', '1.103', '0.3489', '0.4324', '-0.1263', '0.6606', '0.03717', '-0.1958', '0.3577', '0.639', '-1.334', '0.2886', '-0.5073', '0.2438', '-0.1824', '-0.04376', '-0.2206', '0.2888', '0.2076', '-0.2179', '0.0707', '-0.0889', '-0.3486', '0.564', '-0.1353', '-0.0731', '-0.2866', '0.202', '0.3782', '-0.3445', '0.3594', '-0.4595', '0.4802', '0.1398', '-0.7007', '-0.04556', '0.4407', '0.04865', '0.4717', '-0.1537', '0.1785', '0.02', '0.518', '0.03198', '-0.6562', '0.3044', '0.4678', '-0.1774', '0.5684', '-0.5127', '-0.222', '-0.3154', '-0.2412', '-0.1322', '-0.1648', '0.7993', '0.3088', '0.2288', '-0.1871', '0.2196', '-0.00807', '0.03607', '0.10016', '-1.038', '0.425', '0.669', '0.3325', '-0.324', '-0.6353', '-0.9873', '-0.534']",C34704,0004911,,V19.8,,,
mondo:0005440,embryonal carcinoma,"['carcinoma, embryonal, malignant', 'primary extragonadal embryonal carcinoma', 'embryonal carcinoma']",3308,,180226,C0206659,,C3752,0004986,D018236,,,,
mondo:0005441,otitis media,"['middle Ear Inflammation', 'otitis Media', 'medial otitis', 'middle ear inflammation', 'otitis media (disease)']",10754,,,C0029882,,C34885,0004992,D010033,382.9,,,0000388
mondo:0005445,visceral leishmaniasis,"['kala-azar', 'kala-azar susceptibility', 'infection by visceral leishmaniasis', 'viscus leishmaniasis', 'kala-azar, susceptibility to']",9146,,,C0023290,,C34771,0005045,D007898,085.0,B55.0,,
mondo:0005446,cutaneous leishmaniasis,"['Asian desert cutaneous leishmaniasis', 'zone of skin leishmaniasis', 'leproid leishmaniasis']",9111,,,C0023283,,C34770,0005046,D016773,085.2,B55.1,,
mondo:0005447,testicular cancer,"['malignant testicular tumour', 'paediatric testicular neoplasm', 'malignant neoplasm of testis', 'malignant testicular tumor', 'malignant tumour of testis', 'cancer of testis', 'malignant neoplasm of the testis', 'testis cancer', 'testicular tumor', 'testicular tumour', 'malignant tumor of testis', 'testis neoplasm', 'malignant testicular neoplasm', 'malignant testis neoplasm', 'malignant tumour of the testis', 'malignant tumor of the testis']",2998,,,,,C7251,0005088,D013736,186.9,,,
mondo:0005448,hepatitis C induced liver cirrhosis,,,,,,,,0005129,,,,,
mondo:0005449,conduction system disorder,"['disorder of conducting system of heart', 'conducting system of heart disease or disorder', 'disease of conducting system of heart', 'conducting system of heart disease']",,,,,,,0005137,,,,,
mondo:0005451,eating disorder,"['eating disorder', 'feeding and eating disorder']",8670,,,,,C89332,0005203,,307.59,,,
mondo:0005452,bulimia nervosa,"['hyperorexia nervosa', 'bulimia']",12129,,,,,C97162,0005204,D052018,307.51,F50.2,,
mondo:0005453,congenital heart disease,"['congenital heart defect', 'congenital anomaly of heart', 'defect, congenital heart', 'Abnormality, heart', 'congenital heart defects', 'heart abnormalities', 'heart defect', 'heart, malformation Of', 'heart-congenital defect', 'defects, congenital heart', 'heart abnormality', 'abnormalities, heart', 'heart defect, congenital', 'heart malformation']",1682,,,CN169364,"['0.5117', '-0.2324', '0.212', '-0.2043', '0.3145', '-0.5244', '-0.073', '0.6606', '-0.0847', '0.1366', '0.06586', '-0.4136', '0.2206', '0.718', '-0.2244', '-0.66', '-0.86', '0.08136', '-0.3625', '-0.3704', '-0.08124', '0.2487', '-0.2559', '-0.1788', '-0.291', '-0.472', '-0.02632', '0.3506', '0.337', '-0.228', '0.5083', '0.1559', '0.716', '0.04294', '0.1711', '0.1536', '0.1619', '0.3037', '0.483', '-0.2834', '0.07025', '0.5356', '-0.2954', '-0.1262', '0.5225', '-0.2695', '0.0796', '0.6113', '0.02248', '0.0723', '-0.11584', '-0.3801', '0.5225', '-0.0222', '-0.5117', '0.02448', '-0.755', '0.5933', '-0.268', '0.004063', '-0.01715', '0.1565', '0.1815', '0.141', '-0.85', '0.06125', '0.287', '0.2446', '-0.2852', '0.6025', '0.1455', '0.3782', '0.2', '-0.5513', '0.2705', '0.1825', '0.2122', '0.3955', '-0.483', '0.1384', '-0.274', '0.306', '-0.0643', '0.03906', '0.1284', '-0.2023', '0.3909', '-0.07404', '0.2705', '0.1864', '0.0331', '-0.091', '0.259', '0.4058', '0.655', '0.2026', '0.04425', '-0.491', '-0.3389', '0.2202']",C95834,0005207,D006330,746.9,,,
mondo:0005454,lung neuroendocrine neoplasm,"['pulmonary neuroendocrine neoplasm', 'lung neuroendocrine tumor, well differentiated, low or intermediate grade', 'lung neuroendocrine tumor', 'neuroendocrine neoplasm of lung', 'lung neuroendocrine neoplasm', 'lung neuroendocrine tumour', 'pulmonary neuroendocrine tumour', 'lung NET', 'neuroendocrine neoplasm of the lung', 'pulmonary neuroendocrine tumor']",5410,,,C1334452,,C5670,0005220,,209.61,,,
mondo:0005459,human African trypanosomiasis,"['sleeping sickness', 'African sleeping sickness', 'African trypanosomiasis', 'Africam sleeping sickness']",10112,,3385,C0041228,,C84541,0005225,D014353,086.5,,10001461,
mondo:0005460,swine influenza,"['swine flu', 'H1N1 Virus infection', 'H1N1 flu', 'H1N1 Influenza', 'Swine influenza virus caused influenza', 'Influenza A (H1N1) Virus infection', 'Influenza A (H1N1)']",0050211,,,,,C80444,0005226,,,,,
mondo:0005461,endometrium adenocarcinoma,"['endometrioid adenoma or carcinoma', 'adenocarcinoma of endometrium', 'endometrioid adenoma or carcinoma NOS (morphologic abnormality)', 'endometrium adenocarcinoma', 'endometrioid carcinoma of endometrium', 'adenocarcinoma of uterus', 'endometrioid adenomas and carcinomas', 'endometrial adenocarcinoma', 'endometrial adenoacanthoma', 'adenocarcinoma, endometrial, malignant', 'endometrial endometrioid adenocarcinoma', 'adenocarcinoma of the endometrium', 'endometrioid adenomas and carcinomas (morphologic abnormality)', 'endometrial endometrioid adenocarcinoma with squamous differentiation']",2870,,,C1336905,,C7359,0005232,,,,,
mondo:0005462,primitive neuroectodermal tumor,"['primitive neuroectodermal tumour (PNET)', 'PNET', 'neuroepithelioma', 'neuroectodermal tumor', 'neuroectodermal tumour', 'primitive neuroectodermal tumor (PNET)', 'neuroectodermal neoplasm', 'primitive neuroectodermal tumor', 'primitive neuroectodermal neoplasm']",171,,,,,C3716,0005235,D017599,,,,
mondo:0005463,aortic valve calcification,"['aortic valve calcification', 'aortic valve calcification (disease)']",,,,C0428791,,,0005239,,,,,0004380
mondo:0005464,rhegmatogenous retinal detachment,,,,,C0271055,,C118755,0005240,,,,,
mondo:0005465,methamphetamine-induced psychosis,,,,,,,,0005242,,,,,
mondo:0005466,hypersomnia,"['hypersomnia', 'hypersomnia (disease)']",,,,C0917799,,C78346,0005246,,780.54,,,0100786
mondo:0005467,occupation-related stress disorder,,,,,,,,0005250,,,,,
mondo:0005468,hypotensive disorder,"['hypotension', 'hypotension (disease)']",,,,,,,0005251,D007022,458.9,,,0002615
mondo:0005469,orthostatic hypotension,"['orthostatic hypotension (disease)', 'orthostatic hypotension']",,,,,"['-0.0777', '0.05234', '-0.2915', '0.3281', '-0.207', '0.3643', '-0.01622', '0.5215', '-0.346', '0.4385', '0.568', '0.3193', '-0.02376', '0.569', '-0.494', '-0.3843', '-0.506', '0.2328', '0.2347', '-0.1722', '-0.0794', '-0.1776', '0.3137', '0.4258', '-0.10944', '-0.7964', '-0.3406', '-0.0088', '-0.666', '0.1051', '0.2358', '-0.06058', '0.4358', '-0.1443', '-0.617', '0.393', '-0.195', '0.10986', '0.19', '-0.4875', '0.251', '0.002497', '0.1142', '0.278', '0.1896', '-0.6885', '-0.2087', '0.1631', '0.096', '0.239', '-0.1318', '0.2236', '-0.4292', '-0.3152', '0.09045', '0.2966', '0.0746', '0.51', '-0.5664', '0.02786', '-0.2228', '0.8193', '0.167', '-0.446', '-0.3335', '0.35', '0.0495', '0.6416', '-0.3', '0.4397', '-0.1862', '0.839', '-0.2468', '-0.3284', '-0.1621', '0.9297', '0.0932', '0.002867', '-0.2018', '0.4043', '-0.8853', '-0.2128', '0.0538', '0.4485', '0.4705', '-0.2656', '0.1858', '-0.08167', '1.141', '-0.1678', '-0.05862', '-0.5146', '0.3455', '0.2637', '0.859', '0.441', '-0.335', '-0.2136', '-0.5967', '0.1987']",,0005252,,458.0,,,0001278
mondo:0005470,postprandial hypotension,,,,,,,,0005253,,,,,
mondo:0005471,neurally mediated hypotension,,,,,,,,0005254,,,,,
mondo:0005473,temporomandibular joint disorder,['TMD'],,,,,,C63709,0005279,D013705,524.69,,,
mondo:0005475,migraine with aura,['classic migraine'],10024,,,C0154723,,C117005,0005295,D020325,346.00,,,0002077
mondo:0005476,atrioventricular node disorder,"['disorder of atrioventricular node', 'atrioventricular node disease or disorder', 'disease of atrioventricular node', 'atrioventricular node disease']",,,,,,,0005305,,,,,
mondo:0005477,ventricular tachycardia,,,,,C0042514,,C50802,0005306,D017180,,I47.2,,
mondo:0005478,torsades de pointes,,,,,C0040479,,,0005307,D016171,,,,0001664
mondo:0005479,atrial tachycardia,,,,,,,C35481,0005308,,427.89,,,
mondo:0005480,contact dermatitis,"['dermatitis, venenata', 'contact dermatitis', 'contact eczema', 'dermatitis venenata', 'contact dermatitis/eczema']",2773,,,C0011616,,C26743,0005319,D003877,692.9,,,
mondo:0005481,contact dermatitis due to nickel,,,,,C0684345,,,0005320,,,,,
mondo:0005483,chemotherapy-induced alopecia,,,,,,,C164162,0005400,,,,,
mondo:0005484,colorectal adenoma,"['adenoma of large intestine', 'colorectum adenoma', 'adenoma of the large bowel', 'large bowel adenoma', 'large intestine adenoma', 'adenoma of the large intestine', 'adenoma of large bowel', 'colorectal adenoma']",0050914,,,C1302401,,C5673,0005406,,,,,
mondo:0005485,psychotic disorder,"['psychosis', 'mental or behavioral disorder', 'mental or behavioural disorder']",2468,,,,,C78576,0005407,,298.9,,,0000709
mondo:0005486,tooth agenesis,"['selective tooth agenesis', 'hypodontia', 'familial tooth agenesis', 'oligodontia', 'tooth agenesis, selective']",0050591,,99798,CN169366,"['0.2054', '-0.01281', '0.01945', '0.571', '0.6553', '-0.2379', '0.177', '1.039', '-0.2766', '-0.0414', '-0.713', '-0.4346', '0.0729', '0.402', '0.1663', '0.01997', '0.4148', '-0.09814', '-0.582', '-0.8555', '-0.4407', '-0.04483', '0.904', '-0.5938', '0.5503', '-0.07697', '-0.5444', '-0.328', '-0.11127', '-0.2087', '0.2278', '0.28', '-0.2976', '-0.12225', '0.0212', '0.339', '0.2744', '-0.414', '0.05923', '-0.4148', '0.3765', '0.5283', '-0.1649', '-0.611', '0.1688', '-0.3984', '-0.00445', '-0.3198', '-0.05978', '-0.4058', '-0.03455', '-0.4395', '-0.2622', '0.2183', '-0.6436', '0.1558', '0.212', '-0.0936', '-0.4265', '-0.2035', '0.1511', '0.2874', '-0.01263', '-0.4014', '-0.06155', '0.1571', '0.3108', '0.3813', '-0.1669', '-0.06036', '-0.0672', '0.1754', '0.4473', '-0.4312', '0.3496', '-0.2483', '0.4348', '-0.4495', '-0.4172', '-0.4822', '0.0468', '-0.2432', '-0.1622', '0.4822', '-0.02429', '0.2286', '0.1056', '0.2783', '0.3784', '0.3623', '-0.3684', '0.6636', '-0.3936', '0.4453', '0.06476', '-0.4417', '0.2067', '-0.5464', '0.1023', '-0.06995']",,0005410,D000848,520.0,K00.0,,
mondo:0005487,schizoaffective disorder,,5418,,,,,C94378,0005411,,295.7,,,
mondo:0005488,adolescent idiopathic scoliosis,,,,3153,,"['0.3208', '0.09296', '0.04803', '-0.2374', '0.5483', '-0.977', '0.4373', '0.7866', '-1.332', '-0.716', '0.8423', '0.08704', '-0.3154', '1.159', '-0.2128', '-0.00666', '0.09436', '-0.3818', '-0.592', '-0.1225', '0.277', '0.3208', '0.0723', '0.05743', '-0.3713', '-0.2742', '0.273', '-0.005127', '-0.03235', '0.3347', '0.3157', '-0.361', '0.4458', '-0.04962', '-0.1884', '0.03116', '-0.684', '-0.77', '-0.0354', '-0.1637', '0.2323', '0.3184', '-0.5493', '0.2031', '0.3933', '0.3994', '0.0176', '0.356', '0.1722', '0.3208', '0.4456', '0.225', '0.6406', '-0.1637', '-0.1675', '-0.02774', '-0.58', '0.635', '-0.3792', '0.0881', '-0.034', '-0.0544', '0.2961', '0.4487', '-0.187', '0.5327', '-0.09033', '1.19', '-0.1553', '0.4167', '0.3877', '-0.157', '0.3198', '-0.624', '-0.269', '0.8276', '-0.3735', '0.6416', '-0.1562', '-0.418', '-0.1461', '-0.1344', '-0.5527', '-0.03784', '0.1514', '-0.3696', '0.003206', '-0.451', '0.3613', '0.2747', '-0.095', '-0.3604', '-0.2627', '0.5396', '0.902', '0.3916', '0.1998', '-0.03387', '-0.03114', '-0.0868']",,0005423,,,,,
mondo:0005489,dyslexia,"['dyslexia', 'dyslexia (disease)']",4428,,,,"['0.6', '0.1049', '0.861', '0.4622', '-0.375', '-0.2927', '0.01906', '0.516', '-0.675', '-0.3838', '0.5615', '0.2664', '0.12054', '0.6143', '0.7686', '-0.009834', '-0.4834', '0.02423', '-0.0336', '-0.5513', '-0.737', '0.4336', '0.1849', '-0.02234', '0.0107', '-0.5537', '0.0389', '-0.02219', '-0.1697', '0.3506', '0.5864', '-0.4556', '0.4258', '0.8657', '-0.799', '0.4497', '-0.4375', '0.05637', '0.10974', '-1.171', '0.8896', '0.0663', '-0.2122', '-0.101', '0.10443', '-0.3513', '0.4111', '0.02103', '0.4534', '0.5107', '0.1544', '0.1086', '-0.4001', '0.02513', '0.7617', '0.6704', '-0.5625', '0.1674', '-0.4553', '0.3284', '-0.2328', '0.864', '-0.106', '0.4214', '-0.01195', '0.3025', '0.2229', '0.0888', '-0.618', '0.1804', '0.356', '0.2524', '-0.01474', '-0.486', '0.5176', '0.6406', '-0.1383', '0.4749', '-0.3057', '-0.1039', '0.2668', '0.1647', '-0.604', '0.826', '0.551', '0.1279', '-0.3708', '-0.284', '0.66', '0.1962', '-0.4976', '0.525', '-0.4067', '0.2144', '0.624', '0.0384', '0.05615', '-0.4268', '0.3235', '0.2131']",C96410,0005424,D004410,,,,0010522
mondo:0005490,large artery stroke,,,,,,,,0005524,,,,,
mondo:0005491,Chagas cardiomyopathy,['Trypanosoma cruzi caused cardiomyopathy'],,,,,,,0005529,D002598,086.0,,,
mondo:0005492,urticaria,"['Urticarias', 'urticaria (disease)', 'urticaria', 'hives']",1555,,,C0042109,,C3432,0005531,D014581,708.9,L50,,0001025
mondo:0005493,carbon monoxide-induced delayed encephalopathy,['delayed encephalopathy after acute carbon monoxide poisoning'],,,,,,,0005534,,,,,
mondo:0005494,triple-negative breast carcinoma,"['triple-receptor negative breast cancer', 'triple-negative breast cancer', 'triple-negative breast carcinoma']",0060081,,,C3539878,,C71732,0005537,D064726,,,,
mondo:0005495,adrenal gland disorder,"['adrenal gland diseases', 'disease of adrenal gland', 'adrenal gland disease', 'adrenal gland disorder', 'adrenal gland disease or disorder', 'adrenal gland disorders', 'disorder of adrenal gland']",9553,,,,,C26690,0005539,D000307,255.9,,,
mondo:0005496,bile duct carcinoma,"['bile duct cancer', 'bile duct carcinoma', 'carcinoma of bile duct', 'bile duct cancer (including cholangiocarcinoma)']",4897,,,C0740277,,C27814,0005540,,,,,
mondo:0005497,bone development disease,"['bone development disease or disorder', 'disease of bone development', 'bone development disease', 'disorder of bone development']",0080006,,,,,,0005541,,,,,
mondo:0005498,botulism,"['foodborne botulism (subtype)', 'infant botulism (subtype)', 'botulism', 'infection due to Clostridium botulinum', 'intoxication with Clostridium botulinum toxin', 'wound botulism (subtype)', 'botulism poisoning', 'food poisoning due to Clostridium botulinum', 'foodborne botulism']",11976,,1267,C0006057,,C84599,0005542,D001906,,,10006041,
mondo:0005499,brain glioma,"['brain malignant glioma', 'malignant glioma of brain']",0060108,,,C0349661,"['0.6045', '-0.2825', '-0.2119', '0.12476', '0.00553', '0.132', '0.8267', '0.5586', '-0.619', '0.3008', '0.3276', '0.1433', '-0.5684', '0.0882', '0.05856', '-0.2059', '0.0172', '-0.47', '-0.3877', '-0.5034', '-0.1719', '-0.1215', '-0.528', '-0.718', '0.2479', '-0.1938', '-0.2104', '-0.02075', '-0.2291', '-0.1181', '0.5137', '-0.2651', '0.4421', '-0.8867', '0.2129', '-0.1091', '-0.1691', '-0.558', '0.3508', '-0.9937', '0.808', '-0.288', '0.1769', '-0.4456', '0.6724', '0.46', '0.571', '-0.2147', '0.4282', '0.3042', '0.374', '0.39', '-0.1595', '-0.2484', '0.1682', '0.359', '-0.4585', '0.3474', '-0.7275', '-0.2264', '0.0771', '-0.04364', '0.319', '0.293', '-0.1964', '0.452', '0.1312', '0.5347', '-0.2458', '0.876', '-0.251', '0.9395', '0.2426', '-0.3489', '0.8833', '0.2932', '0.0908', '0.3572', '0.3557', '0.01294', '0.2715', '0.1175', '-0.4595', '0.6953', '-0.2998', '-0.6577', '0.532', '-0.0529', '0.807', '-0.01487', '-0.11816', '0.3333', '-0.3145', '-0.2507', '0.6143', '0.2305', '-0.2076', '-0.3152', '-0.6187', '-0.2278']",,0005543,,,,,
mondo:0005500,congenital disorder of glycosylation type I,"['DPM3-CDG', 'MPI-CDG (CDG-1b)', 'ALG3-CDG (CDG-1d)', 'ALG1-CDG', 'ALG11-CDG (CDG-1p)', 'PMM2-CDG (CDG-1a)', 'ALG9-CDG (CDG-1l)', 'DPAGT1-CDG (CDG-1j)', 'MPI-CDG', 'RFT1-CDG (CDG-1n)', 'MPDU1-CDG (CDG-1f)', 'ALG3-CDG', 'MPDU1-CDG', 'ALG2-CDG (CDG-1i)', 'ALG12-CDG', 'DOLK-CDG (CDG-1m)', 'ALG11-CDG', 'congenital disorders of glycosylation, type I', 'ALG8-CDG', 'SRD5A3-CDG', 'ALG2-CDG', 'ALG9-CDG', 'DPM3-CDG (CDG-1o)', 'DOLK-CDG', 'ALG8-CDG (CDG-1h)', 'DPM1-CDG', 'RFT1-CDG', 'DPM1-CDG (CDG-1e)', 'PMM2-CDG', 'ALG6-CDG (CDG-1c)', 'SRD5A3-CDG (CDG-1q)', 'ALG12-CDG (CDG-1g)', 'DPAGT1-CDG', 'ALG6-CDG', 'DPM2-CDG', 'ALG1-CDG (CDG-1k)', 'DPM2-CDG (CDG-1u)']",0050570,,,,"['-0.1937', '0.06555', '0.076', '0.0675', '0.1721', '-0.1892', '-0.02959', '0.02402', '-0.1918', '0.03763', '-0.1344', '-0.06586', '0.1214', '-0.01895', '-0.1399', '-0.10205', '0.04764', '-0.1543', '-0.08655', '-0.3179', '0.01788', '0.0366', '0.2874', '-0.1198', '0.004955', '-0.05176', '0.008316', '-0.1383', '0.05798', '-0.05124', '0.1941', '0.2289', '0.2043', '0.1354', '-0.05933', '-0.1103', '0.03607', '-0.003384', '-0.116', '-0.2898', '0.0823', '-0.2786', '0.014435', '0.03165', '-0.1064', '-0.2292', '0.09247', '0.1945', '0.1656', '0.1482', '-0.1228', '-0.0714', '0.09814', '-0.004803', '-0.1564', '-0.1556', '0.1858', '-0.00511', '-0.2451', '0.0904', '0.10077', '0.0769', '0.2118', '-0.02184', '0.02739', '-0.03418', '0.2153', '0.02467', '-0.2323', '0.01729', '-0.11053', '0.0679', '-0.09607', '-0.09216', '0.1262', '0.1063', '0.05038', '0.01999', '-0.2494', '-0.01454', '0.0618', '-0.059', '-0.1649', '0.1311', '-0.02394', '-0.09607', '0.07104', '0.1989', '0.1311', '-0.0989', '-0.007595', '0.3044', '-0.0472', '-0.07855', '0.3032', '0.05753', '0.2246', '-0.3362', '0.01274', '0.251']",,0005545,,,,,
mondo:0005501,congenital disorder of glycosylation type II,"['B4GALT1-CDG', 'MOGS-CDG', 'B4GALT1-CDG (CDG-2d)', 'congenital disorders of glycosylation, type II', 'MOGS-CDG (CDG-2b)', 'MGAT2-CDG (CDG-2a)', 'MGAT2-CDG']",0050571,,,,"['-0.1636', '0.0989', '0.0891', '0.04895', '0.1019', '-0.1888', '-0.001834', '-0.00963', '-0.1919', '0.0153', '-0.1272', '-0.08234', '0.1405', '-0.03687', '-0.1931', '-0.02954', '0.02657', '-0.1388', '-0.095', '-0.3992', '-0.053', '-0.07654', '0.3054', '-0.08984', '0.03766', '-0.0307', '-0.0741', '-0.1881', '0.0974', '-0.1714', '0.02356', '0.2764', '0.1862', '0.1387', '-0.04425', '-0.1652', '-0.02101', '-0.02058', '-0.09784', '-0.2214', '0.004288', '-0.3186', '-0.02959', '0.1094', '-0.04932', '-0.248', '0.011604', '0.2067', '0.2291', '0.153', '-0.1227', '-0.1153', '0.1055', '-0.02364', '-0.1403', '-0.1385', '0.1792', '0.06058', '-0.1771', '0.0659', '0.0824', '0.0736', '0.2477', '0.04663', '-0.04355', '-0.01924', '0.1871', '0.1272', '-0.263', '0.03238', '-0.1609', '0.1515', '0.01354', '-0.0641', '0.122', '0.1122', '0.0845', '-0.0521', '-0.1763', '0.02588', '0.06067', '-0.079', '-0.1449', '0.1888', '-0.1129', '-0.032', '0.0261', '0.1904', '0.1697', '-0.0749', '0.02962', '0.2294', '0.03992', '0.01122', '0.3093', '0.1753', '0.2208', '-0.3145', '0.01157', '0.1271']",,0005546,C535747,,,,
mondo:0005502,dengue disease,"['Dengue fever', 'break bone fever', 'Dengue virus caused disease or disorder', 'breakbone fever', 'classic dengue', 'Thai hemorrhagic fever', 'hemorrhagic dengue', 'Philippine hemorrhagic fever', 'Dengue', 'Singapore hemorrhagic fever', 'DF', 'Dengue virus infection', 'classical dengue']",12205,,99828,C0011311,,C34528,0005547,D003715,061,,10012310,
mondo:0005503,developmental disorder of mental health,,0060037,,,,,,0005548,,315.8,,,
mondo:0005504,diphtheria,['Corynebacterium infection'],11405,,1679,C0012546,,C34541,0005549,D004165,032.9,A36.3,10013023,
mondo:0005505,dysembryoplastic neuroepithelial tumor,"['dysembryoplastic neuroepithelial neoplasm', 'dysembryoplastic neuroepithelial tumour (morphologic abnormality)', 'DNT', 'DNET', 'dysembryoplastic neuroepithelial tumor (morphologic abnormality)']",2679,,251946,C1266177,,C9505,0005551,,,,,
mondo:0005506,eccrine sweat gland cancer,"['malignant eccrine skin neoplasm', 'malignant neoplasm of eccrine sweat gland', 'malignant eccrine tumor', 'malignant eccrine neoplasm of skin', 'malignant eccrine skin tumor', 'malignant eccrine tumour of the skin', 'malignant eccrine sweat gland neoplasm', 'malignant eccrine skin tumour', 'malignant eccrine tumor of skin', 'cancer of eccrine sweat gland', 'malignant eccrine tumor of the skin', 'malignant eccrine neoplasm', 'malignant eccrine neoplasm of the skin', 'eccrine sweat gland cancer', 'malignant eccrine tumour of skin', 'malignant eccrine tumour']",4921,,,C1334577,,C5559,0005553,,,,,
mondo:0005507,gingival cancer,"['malignant tumour of the gingiva', 'malignant neoplasm of gum', 'gingiva cancer', 'malignant tumor of gum', 'malignant tumour of the gum', 'malignant gingiva neoplasm', 'malignant tumour of gingiva', 'malignant tumour of gum', 'gum cancer', 'malignant gum tumour', 'malignant gum neoplasm', 'malignant gum tumor', 'malignant neoplasm of gingiva', 'malignant gingival neoplasm', 'malignant tumor of the gingiva', 'malignant gingival tumor', 'malignant neoplasm of the gum', 'malignant neoplasm of the gingiva', 'malignant tumor of gingiva', 'cancer of gingiva', 'malignant gingival tumour', 'malignant tumor of the gum', 'malignant neoplasm of other sites of gum']",8602,,,C0153364,,C9317,0005557,,143.9,,10067807,
mondo:0005508,hereditary multiple osteochondromas,"['HMO', 'multiple cartilaginous exostoses', 'hereditary multiple exostosis', 'multiple ostechondromas', 'hereditary multiple exostoses 1', 'osteochondromatosis syndrome (disorder) [ambiguous]', 'multiple exostoses', 'hereditary multiple exostoses 3', 'hereditary multiple exostoses', 'EXT', 'multiple congenital exostosis', 'osteochondromatosis syndrome', 'Bessel-Hagen disease', 'multiple exostosis syndromes', 'hereditary multiple exostoses 2']",206,,321,CN204014,"['-0.5566', '0.1818', '-0.1364', '-0.2164', '0.253', '0.1465', '0.154', '1.1875', '-0.981', '-0.0505', '0.1371', '0.789', '0.0931', '0.4124', '0.04532', '0.1256', '0.01024', '-0.3801', '-0.2052', '-0.424', '-0.2876', '0.2426', '1.004', '-0.6675', '-0.05908', '-0.05734', '-0.0181', '-0.11896', '-0.04337', '0.1853', '0.2328', '-0.2969', '-0.2456', '0.04697', '-0.3486', '0.3083', '-0.02531', '-0.68', '0.39', '0.00842', '0.7583', '-0.4404', '0.5303', '-0.4546', '0.483', '-0.5513', '-0.532', '-0.1191', '0.3333', '-0.1743', '0.595', '-0.2375', '0.01397', '0.04605', '-0.1951', '-0.276', '0.09564', '0.823', '-0.3452', '0.3218', '0.682', '0.4392', '-0.6465', '0.7554', '-0.3152', '0.9517', '0.897', '0.696', '0.1766', '0.3271', '0.2072', '-0.0327', '0.3074', '-0.2129', '0.2427', '0.3157', '-0.07117', '0.664', '-0.092', '-0.7505', '-0.6777', '0.0048', '-0.406', '0.3472', '-0.7485', '-0.3218', '0.2314', '-0.3386', '-0.588', '-0.1504', '-0.04138', '0.01094', '-0.5557', '0.02881', '1.048', '0.0812', '1.151', '-0.554', '0.1215', '-0.1691']",C5183,0005560,D005097,,,,
mondo:0005509,histiocytoma,['histiocytoma'],4231,,,C1509147,"['-0.1366', '0.139', '0.115', '0.003002', '0.06506', '-0.097', '0.0702', '0.0661', '-0.02557', '-0.0485', '-0.03674', '0.02614', '0.008766', '0.01025', '-0.09247', '-0.10205', '-0.0645', '-0.05118', '-0.0274', '-0.2439', '0.011734', '-0.1382', '0.1506', '-0.05484', '0.03912', '-0.0872', '-0.03806', '-0.02531', '-0.08484', '-0.0901', '0.0984', '0.03864', '0.1527', '-0.05612', '0.08984', '0.005726', '-0.0468', '0.06067', '-0.01022', '-0.2389', '0.05273', '-0.1517', '0.05676', '-0.1169', '0.001421', '-0.0876', '-0.02452', '0.07684', '0.12103', '0.02354', '0.08026', '-0.01098', '0.006218', '0.0867', '-0.1063', '-0.0791', '0.1201', '-0.05408', '-0.2435', '0.04114', '0.1411', '0.0507', '-0.09705', '0.04636', '-0.0188', '0.01659', '0.1989', '0.10767', '-0.0957', '0.184', '-0.02126', '0.02306', '0.0977', '-0.04895', '0.001657', '0.0497', '-0.01819', '0.07996', '-0.0863', '-0.2308', '-0.1085', '-0.01458', '-0.0626', '0.07886', '-0.181', '-0.1037', '0.07', '0.09863', '0.0762', '-0.05124', '0.08093', '0.1093', '-0.00876', '0.002996', '0.295', '0.01888', '0.0901', '-0.1879', '-0.0997', '0.0488']",C35765,0005561,D051642,,,,
mondo:0005510,hydronephrosis,,11111,,,C0020295,,C26796,0005562,D006869,591,,,
mondo:0005511,janus kinase-3 deficiency,,0060008,,,,,,0005565,,,,,
mondo:0005512,malignant peritoneal mesothelioma,"['advanced peritoneal malignant mesothelioma', 'peritoneum malignant mesothelioma (disease)', 'peritoneal mesothelioma', 'diffuse malignant peritoneal mesothelioma', 'advanced malignant peritoneal mesothelioma', 'primary malignant peritoneal mesothelioma', 'advanced malignant mesothelioma of the peritoneum', 'malignant peritoneal mesothelioma, advanced', 'malignant mesothelioma of peritoneum', 'peritoneal mesothelioma (disease), malignant', 'advanced malignant mesothelioma of peritoneum']",1788,,168811,,,C8704,0005567,,,,10056558,
mondo:0005514,nanophthalmia,,0080634,,35612,,"['-0.2927', '-0.172', '-0.1403', '-0.2256', '0.04007', '0.3433', '0.03986', '0.6035', '-0.3828', '-0.5903', '0.1609', '-0.2817', '0.01072', '0.02667', '-0.0695', '0.05225', '0.484', '-0.1361', '0.3015', '-0.6436', '-0.286', '-0.0764', '0.1731', '0.1434', '0.09674', '0.3767', '-0.161', '0.4124', '0.2283', '0.6494', '0.349', '-0.2727', '0.342', '0.2964', '-0.4019', '0.2471', '0.1481', '-1.171', '0.3533', '-0.423', '-0.01035', '-0.4946', '0.6924', '-0.5244', '-0.2363', '-0.2272', '0.04135', '-0.2878', '0.1523', '-0.07446', '0.497', '-0.1415', '-0.874', '-0.76', '-0.0491', '-0.0815', '0.3992', '-0.4539', '-0.7393', '-0.3164', '0.10657', '-0.4668', '0.1279', '0.4397', '-0.03928', '0.1825', '0.1615', '0.4705', '-0.151', '0.3877', '-0.1098', '0.286', '0.4736', '-0.03394', '0.2152', '0.361', '0.3687', '0.1334', '0.10693', '0.2076', '-0.3347', '0.6777', '-0.309', '0.7583', '0.02339', '-0.1627', '0.1372', '-0.01017', '0.1333', '0.6133', '-0.00387', '0.2764', '-0.05472', '0.248', '1.128', '-0.4463', '0.543', '-0.453', '-0.2732', '-0.2043']",,,,,,,
mondo:0005515,oral cavity cancer,"['malignant oral cavity tumour', 'malignant mouth tumour', 'malignant mouth neoplasm', 'malignant neoplasm of lateral floor of mouth', 'malignant tumor of anterior floor of mouth', 'malignant oral cavity tumor', 'malignant tumour of anterior floor of mouth', 'malignant mouth tumor', 'cancer of oral cavity', 'malignant oral cavity neoplasm', 'malignant tumor of the floor of the mouth', 'malignant neoplasm of mouth', 'malignant neoplasm of lateral portion of floor of mouth', 'malignant tumour of lateral floor of mouth', 'malignant tumor of the mouth', 'malignant tumour of the floor of the mouth', 'oral cavity cancer', 'malignant neoplasm of oral cavity', 'malignant tumor of mouth', 'malignant neoplasm of floor of mouth', 'malignant neoplasm of anterior portion of floor of mouth', 'malignant tumour of the mouth', 'malignant tumour of mouth', 'malignant tumour of oral cavity', 'malignant neoplasm of the mouth', 'malignant tumor of lateral floor of mouth']",8618,,,,,C9314,0005570,,149.8,,,
mondo:0005516,osteochondrodysplasia,"['cartilage development disorder', 'skeletal dysplasia', 'osteochondrodysplasia syndrome', 'congenital anomaly of cartilage', 'osteochondrodysplasia', 'congenital skeletal dysplasia']",2256,,,C0029422,"['-0.1898', '0.1418', '0.2074', '-0.1929', '0.2', '-0.161', '-0.05154', '0.3262', '-0.2467', '-0.05627', '-0.1071', '-0.03354', '0.1134', '0.02148', '-0.1197', '-0.1437', '0.0958', '-0.006847', '-0.194', '-0.369', '0.01176', '0.000787', '0.3005', '-0.174', '-0.0027', '-0.05667', '-0.0572', '-0.0105', '0.03674', '-0.10754', '0.00818', '0.0102', '0.1753', '0.0363', '0.02661', '-0.01907', '-0.03458', '-0.1065', '-0.0789', '-0.2495', '0.1573', '-0.156', '-0.04657', '-0.08606', '-0.0469', '-0.2186', '0.08984', '0.2144', '0.273', '0.07153', '0.0602', '-0.007763', '0.1139', '0.1478', '-0.1205', '-0.2727', '-0.06476', '0.01709', '-0.1722', '0.04993', '0.3394', '0.0912', '-0.08984', '0.0919', '-0.1134', '-0.0159', '0.2615', '0.1907', '-0.253', '0.1816', '-0.08435', '-0.02522', '0.1086', '-0.12085', '0.00788', '0.11804', '-0.08185', '0.2068', '-0.2007', '-0.1835', '-0.05225', '-0.05734', '-0.0351', '0.1525', '-0.2598', '-0.02219', '0.06042', '0.1754', '0.1825', '0.01884', '-0.0002028', '0.2642', '-0.04807', '0.1393', '0.2083', '0.1759', '0.1619', '-0.2632', '0.1255', '0.08673']",C84978,0005571,D010009,756.4,,,
mondo:0005517,pharynx cancer,"['malignant pharynx tumour', 'malignant tumor of the pharynx', 'cancer of chordate pharynx', 'malignant tumour of the pharynx', 'malignant pharyngeal tumor', 'malignant pharynx neoplasm', 'pharynx neoplasm', 'cancer of pharynx', 'pharyngeal cancer', 'pharyngeal neoplasm', 'malignant pharyngeal tumour', 'malignant pharynx tumor', 'malignant pharyngeal neoplasm', 'malignant neoplasm of pharynx', 'malignant chordate pharynx neoplasm', 'malignant tumor of pharynx', 'malignant neoplasm of chordate pharynx', 'pharynx cancer', 'malignant tumour of pharynx']",0060119,,,,,C7545,0005577,D010610,,,,
mondo:0005518,pseudohermaphroditism,['indeterminate sex and pseudohermaphroditism'],3765,,,,,C124575,0005579,,752.7,Q56.3,,
mondo:0005519,renal pelvis carcinoma,"['carcinoma of the renal pelvis', 'cancer of renal pelvis', 'malignant tumour of renal pelvis', 'carcinoma of kidney pelvis', 'kidney renal pelvis cancer', 'carcinoma of renal pelvis', 'renal pelvis carcinoma', 'malignant neoplasm of renal pelvis', 'kidney pelvis carcinoma', 'malignant renal pelvis neoplasm', 'renal pelvis cancer', 'carcinoma of the kidney pelvis']",4919,,,C1335749,,C6142,0005582,,189.1,C65,,
mondo:0005520,rickets,"['nutritional rickets', 'active rickets', 'rickets (disease)', 'rachitis', 'vitamin D deficiency disease', 'vitamin-D deficiency rickets', 'rickets', 'hypovitaminosis D', 'vitamin D hydroxylation-deficient rickets']",10609,,,C0221468,,C26878,0005583,D012279,268.0,,,0002748
mondo:0005522,small intestine carcinoma,"['small bowel carcinoma', 'small intestine cancer', 'small intestinal cancer', 'cancer of the small bowel', 'cancer of small bowel', 'small intestine carcinoma', 'small intestine cancer, NOS', 'carcinoma of the small bowel', 'carcinoma of small bowel', 'small bowel cancer', 'small intestinal carcinoma', 'carcinoma of the small intestine', 'carcinoma of small intestine']",4907,,,,,C7724,0005588,,,,,
mondo:0005523,steroid inherited metabolic disorder,,1701,,,C1257809,,,0005590,D043202,,,,
mondo:0005524,sweat gland carcinoma,"['carcinoma, sweat gland, malignant', 'carcinoma of the sweat gland', 'sweat gland carcinoma', 'sweat gland carcinoma/apocrine eccrine carcinoma', 'carcinoma of sweat gland']",5667,,,C1412016,,C6938,0005591,,,,,
mondo:0005525,T-cell leukemia,"['leukaemia (disease) of T cell', 'T cell leukemia (disease)', 'T cell leukaemia (disease)']",715,,,C0023492,,C8694,0005592,D015458,,,,
mondo:0005526,tetanus,"['Clostridium tetani caused infectious disease of the nervous system', 'infection due to Clostridium tetani', 'lockjaw', 'clostridial tetanus']",11338,,3299,C0039614,,C85185,0005593,D013742,037,,10043376,
mondo:0005527,toxic encephalopathy,"['neurotoxicity syndrome', 'neurotoxicity syndromes', 'neurotoxicity']",3602,,,,,C27961,0005595,D020258,349.82,G92,,
mondo:0005528,inborn vitamin metabolic disorder,"['rare inborn error of vitamin metabolic process', 'vitamin metabolic disorder', 'inborn error of vitamin metabolic process']",0050718,,,,,,0005596,,,,,
mondo:0005530,opiate dependence,['opioid type dependence'],2559,,,,,,0005611,D009293,304.00,,,
mondo:0005531,morphine dependence,,2560,,,,,,0005612,D009021,,,,
mondo:0005532,Crohn^s colitis,['Crohn colitis'],0060192,,,,,C35211,0005622,,555.1,,,
mondo:0005533,distal colitis,['left colon inflammation'],,,,C0860168,,,0005623,,558.9,,,
mondo:0005534,ileocolitis,,0060190,,,C0949272,,,0005624,,,,10062647,
mondo:0005535,oral Crohn disease,['oral Crohn^s disease'],,,,C0399497,,,0005625,,,,,
mondo:0005536,pancolitis,"['pan-ulcerative colitis', 'universal colitis']",,,,,,,0005626,,,,,
mondo:0005537,perianal Crohn disease,['perianal Crohn^s disease'],,,,C0341395,,,0005627,,,,,
mondo:0005538,proctitis,"['anus inflammation', 'rectitis']",3127,,,C0033246,,C38011,0005628,D011349,569.49,,,
mondo:0005539,small bowel Crohn disease,['small bowel Crohn^s disease'],,,,,,,0005629,,,,,
mondo:0005541,spondylolysis,"['spondylolysis (disease)', 'spondylolysis']",2300,,,C0038018,,C35034,0005649,D013169,,,,0003304
mondo:0005542,acute coronary syndrome,"['acute coronary syndromes', 'coronary syndrome, acute', 'acute coronary syndrome', 'syndromes, acute coronary', 'coronary syndromes, acute', 'syndrome, acute coronary']",,,,C0948089,,C53652,0005672,D054058,,,,
mondo:0005543,autoimmune hepatitis type 1,['type 1 AIH'],,,563576,,,,,,571.49,,,
mondo:0005544,hippocampal sclerosis of aging,,,,,,,,0005678,,,,,
mondo:0005545,staphylococcus aureus infection,,,,,,,C122576,0005681,,,,,
mondo:0005546,fibromyalgia,"['fibromyalgia syndrome', 'fibromyalgia']",631,,41842,C0016053,,C87497,0005687,D005356,729.1,M79.7,,
mondo:0005549,renal cell adenocarcinoma,"['RCC', 'renal cell carcinoma', 'kidney adenocarcinoma', 'adenocarcinoma of kidney', 'renal cell cancer', 'adenocarcinoma of the kidney', 'renal cell carcinoma, stage unspecified', 'renal cell adenocarcinoma', 'carcinoma, renal cell, malignant']",,,,,,C9385,0005708,,,,,
mondo:0005550,infectious disease,"['clinical infection', 'infectious disorder', 'infectious diseases and manifestations', 'infectious disease', 'communicable disease', 'transmissible disease', 'disease by infectious agent', 'infectious', 'infection']",0050117,,,,,C26726,0005741,D003141,136.9,A00-B99,,
mondo:0005551,eye allergy,,,,,,,,0005751,,,,,
mondo:0005552,ocular vascular disorder,"['vasculature of eye disease', 'disorder of vasculature of eye', 'vasculature of eye disease or disorder', 'ocular vascular disorder', 'disease of vasculature of eye']",,,,,,C35664,0005753,,,,,
mondo:0005554,rheumatic disorder,"['collagen vascular disease', 'disease, rheumatic', 'enthesopathies', 'musculoskeletal pain disorder', 'rheumatism', 'diseases, rheumatic', 'rheumatic disease', 'enthesopathy', 'inflammatory rheumatism', 'connective tissue disease', 'collagen disease', 'rheumatologic disorder']",1575,,,C0035435,,C27204,0005755,D012216,729.0,,,
mondo:0005555,cycloplegia,"['paresis of accommodation', 'ciliary muscle paresis', 'cycloplegic paralysis of accommodation']",10033,,,C0235238,,,0005758,,367.51,,,
mondo:0005556,lupus nephritis,"['nephritis, lupus', 'glomerulonephritis, lupus', 'SLE nephritis', 'lupus nephritis', 'lupus glomerulonephritis', 'lupus Nephritides', 'lupus Glomerulonephritides', 'Nephritides, lupus', 'Glomerulonephritides, lupus']",0080162,,,C0024143,,C34789,0005761,D008181,,,,
mondo:0005557,calcium metabolic disease,['calcium metabolism disease'],10575,,,C0006705,,,0005769,D002128,275.49,,,
mondo:0005558,ovarian disorder,"['ovary disease', 'disorder of ovary', 'ovarian disorder', 'disease of ovary', 'ovary disease or disorder', 'ovarian disease']",1100,,,C0029928,,C26841,0005771,D010049,,,,
mondo:0005559,neurodegenerative disease,"['degenerative disorder of central nervous system', 'central nervous system degenerative disorder', 'central nervous system neurodegenerative disorder', 'degenerative disease', 'cerebral degeneration disease', 'brain degeneration', 'neurodegenerative disease']",1289,,,,,C4802,0005772,D019636,349.89,,,
mondo:0005560,brain disorder,"['encephalopathy', 'brain disease', 'disease of brain', 'brain disease or disorder', 'disorder of brain']",936,,,C0085584,,C96413,0005774,D001927,348.9,,,
mondo:0005561,aortic disorder,"['aorta disease or disorder', 'disorder of aorta', 'disease of aorta', 'aortic disorder', 'aorta disease', 'disorder of the aorta']",520,,,C0003493,,C101253,0005775,D001018,447.9,,,
mondo:0005562,age-related hearing impairment,['ARHI'],,,,,,,0005782,,,,,
mondo:0005563,nut midline carcinoma,"['Midline carcinoma of children and Young adults with NUT rearrangement', 'NUT Midline carcinoma', 'NMC', 'nuclear protein in testis midline carcinoma', 'carcinoma with t(15;19)(q13;p13.1) translocation', 'NUT midline carcinoma of the head and neck', 'NUT carcinoma']",0060463,,443167,CN237663,,C45716,0005783,,,,,
mondo:0005564,embryonal neoplasm,"['embryonal neoplasm', 'embryonal tumor', 'embryonal cancer', 'embryo neoplasm', 'EMBT', 'embryonal tumour']",688,,,C0027654,,C3264,0005784,D009373,,,,
mondo:0005565,blastoma,"['blastoma', 'embryoma']",4766,,,C0936282,,C8997,0005785,,,,,
mondo:0005566,neonatal abstinence syndrome,"['neonatal withdrawal', 'drug withdrawal syndrome in newborn', 'NAS', 'neonatal narcotic withdrawal syndrome']",9828,,,C0027609,,C87101,0005799,D009357,779.5,,,
mondo:0005567,substance withdrawal syndrome,"['drug withdrawal', 'substance withdrawal syndrome', 'withdrawal syndrome', 'substance withdrawal disorder', 'withdrawal disorder']",0060001,,,C0152128,,C35046,0005800,D013375,292.0,,,
mondo:0005568,cholesterol embolism,"['trash foot', 'purple toe syndrome', 'atheroembolism', 'cholesterol crystal embolism', 'warfarin blue toe syndrome']",1461,,,C0585266,,,0005801,D017700,459.89,,,
mondo:0005570,hematologic disorder,"['hematopoietic disease', 'disease or disorder of haematopoietic system', 'haematopoietic system disease', 'haematological system disease', 'hematological disease', 'disorder of haematopoietic system', 'hematological disorders and malignancies', 'haematological disorder', 'hematopoietic system disease or disorder', 'hematologic disorder', 'disease of hematopoietic system', 'blood disorder', 'hematopoietic system disease', 'disease of haematopoietic system', 'blood dyscrasia', 'haematopoietic disease', 'disease of the blood and blood-forming organs', 'blood disease', 'haematological disorders and malignancies', 'haematological disease', 'hematologic and lymphocytic disorder', 'haematopoietic system disease or disorder', 'rare hematologic disease', 'hematological system disease', 'disorder of hematopoietic system', 'hematological disorder']",74,,97992,CN882913,,C26323,0005803,D006402,289.9,D50-D89,,
mondo:0005571,polycythemia,"['erythrocythemia', 'polycythemia (disease)', 'polycythemia']",8432,,98427,C0032461,,C26863,0005804,D011086,,,10036051,0001901
mondo:0005572,polycythemia due to hypoxia,,2835,,,C0856818,,C27312,0005805,,,,,
mondo:0005574,tauopathy,,680,,,C0949664,,,0005815,D024801,,,,
mondo:0005575,colorectal cancer,"['cancer of the large bowel', 'malignant large bowel neoplasm', 'malignant neoplasm of large intestine', 'colorectum cancer', 'colorectal cancer', 'cancer of large bowel', 'colorectal cancer, susceptibility to, autosomal dominant, somatic mutation', 'cancer of colorectum', 'colon cancer, advanced, somatic', 'malignant large intestine tumour', 'cancer of large intestine', 'malignant large intestine tumor', 'malignant tumor of large intestine', 'colon cancer, somatic', 'large intestine cancer', 'malignant tumour of large bowel', 'malignant tumour of the large bowel', 'malignant neoplasm of colorectum', 'malignant colorectal tumour', 'malignant tumour of the large intestine', 'colorectal cancer with chromosomal instability, somatic', 'malignant tumor of large bowel', 'malignant large bowel tumour', 'malignant colorectum neoplasm', 'malignant neoplasm of the large bowel', 'malignant tumor of the large bowel', 'malignant colorectal tumor', 'malignant tumor of the large intestine', 'malignant tumour of large intestine', 'malignant large bowel tumor', 'malignant neoplasm of large bowel', 'malignant large intestine neoplasm', 'colon cancer, susceptibility to, autosomal dominant, somatic mutation', 'malignant neoplasm of the large intestine', 'colon cancer', 'colorectal cancer, autosomal dominant, somatic mutation', 'malignant colorectal neoplasm', 'colorectal cancer, somatic', 'CRC']",9256,114500,466667,C1527249,"['0.1692', '-0.1328', '-0.1583', '0.4954', '0.6133', '-0.8374', '0.536', '0.5513', '0.01195', '0.01993', '0.645', '0.3372', '-0.3376', '0.613', '-0.2081', '-0.1427', '-0.1927', '-0.571', '-0.8467', '-0.487', '0.10754', '-0.7114', '-0.4714', '-0.1415', '0.4067', '-0.777', '0.3516', '0.1154', '0.382', '0.0469', '0.58', '-0.4998', '0.1247', '-0.8755', '0.7246', '-0.236', '-1.1455', '0.3213', '-0.3079', '-0.2769', '0.2932', '-0.1407', '0.2333', '0.1279', '-0.02916', '-0.10223', '-0.1362', '-0.875', '1.602', '-0.1826', '0.04114', '-0.3877', '0.1887', '-0.2052', '-0.4338', '0.2034', '-0.1948', '0.3672', '-1.042', '-0.952', '0.645', '0.01154', '-0.3086', '-0.4548', '-0.3745', '0.6245', '0.4014', '0.3245', '-0.1482', '0.941', '0.00492', '1.029', '0.01646', '-0.1534', '1.383', '0.4333', '-0.0545', '0.121', '-0.132', '0.3396', '-0.1398', '0.4814', '-0.263', '-0.0595', '-0.004665', '-0.1714', '0.8125', '0.3105', '0.8403', '-0.3916', '-0.0611', '-0.05133', '-0.1716', '0.401', '0.045', '0.376', '-0.4607', '-0.915', '-0.4995', '-0.0742']",C4978,0005842,,,,,
mondo:0005576,cryoglobulinemia,"['Cryoimmunoglobulinaemia', 'cryoglobulinemia']",2917,,,C0010403,,C26736,0005846,D003449,273.2,D89.1,,
mondo:0005578,arthritic joint disease,"['arthritis', 'skeletal joint inflammation', 'inflammatory disorder of joint']",848,,,C0003864,,C2883,0005856,D001168,,,,
mondo:0005579,"epilepsy, idiopathic generalized","['generalised epilepsy', 'epilepsy, idiopathic generalized', 'idiopathic generalised epilepsy', 'idiopathic generalized epilepsy', 'EIG', 'generalized epilepsy']",1827,600669,,,"['0.9014', '0.1448', '-0.1282', '-0.16', '-0.53', '-0.3733', '0.9087', '0.0974', '-0.651', '-0.2805', '-0.00469', '-0.2954', '-0.4316', '0.301', '0.0984', '0.2157', '-0.3206', '-0.581', '-0.3943', '-0.572', '-0.2673', '0.6743', '0.2866', '-0.563', '-0.3264', '-0.073', '-0.107', '0.01807', '-0.645', '0.483', '0.271', '-0.6123', '0.3804', '0.1564', '0.9062', '0.526', '-0.2224', '-0.003849', '-0.06805', '-0.5947', '-0.2083', '-0.3315', '0.2057', '-0.232', '-0.3794', '-0.6587', '-0.238', '0.3271', '0.623', '0.634', '-0.3027', '0.2467', '0.06168', '-0.3376', '-0.04993', '-0.351', '-0.1865', '0.1011', '-0.1589', '0.4653', '-0.899', '0.6133', '0.7827', '-0.253', '-0.2385', '1.504', '0.0364', '0.1683', '-0.8496', '0.5625', '0.9497', '0.9985', '-0.0717', '-0.3345', '0.3286', '0.6797', '0.973', '0.535', '-0.557', '0.3286', '-0.1373', '0.8174', '0.5264', '0.4248', '0.5195', '0.0524', '0.2107', '0.8555', '0.771', '0.516', '-0.1288', '0.05988', '-0.2605', '0.2491', '0.1646', '0.2218', '0.4683', '-0.832', '0.2476', '0.3882']",C3021,0005917,C562694,,,,
mondo:0005580,esophageal squamous cell carcinoma,"['squamous cell car. - esophagus', 'esophageal scc', 'squamous cell carcinoma of oesophagus', 'squamous cell carcinoma of the oesophagus', 'esophageal squamous cell cancer', 'oesophagus scc', 'scc of the esophagus', 'oesophagus squamous cell carcinoma', 'esophageal squamous cell carcinoma', 'esophagus scc', 'scc of oesophagus', 'esophagus squamous cell carcinoma', 'squamous cell carcinoma of esophagus', 'scc of the oesophagus', 'ESCC', 'squamous cell carcinoma of the esophagus', 'squamous cell car. - oesophagus', 'esophageal epidermoid carcinoma', 'scc of esophagus']",3748,,99977,C0279626,"['0.2001', '0.1134', '-0.4534', '0.00932', '-0.1483', '-0.34', '0.7817', '0.3599', '-1.062', '-0.6235', '0.1453', '-0.2793', '-0.7285', '0.4304', '-0.5977', '-0.2102', '-0.6006', '-1.164', '-0.2825', '-0.4126', '-0.5527', '-0.5513', '0.3623', '-0.2141', '0.567', '0.1643', '-0.2756', '0.3442', '-0.5117', '-0.01724', '0.3489', '0.02782', '-0.1112', '-0.2443', '0.3792', '-0.05093', '0.1104', '-0.3354', '-0.1271', '-0.2102', '-0.1831', '-0.06964', '0.1868', '-0.09576', '0.609', '0.2184', '-0.5723', '-0.0477', '0.0975', '0.3035', '-0.0681', '-0.1476', '0.07764', '-0.511', '-0.2866', '0.4812', '0.1678', '0.599', '-0.3618', '0.35', '0.2944', '0.4558', '-0.2164', '-0.1058', '-0.10425', '-0.1487', '0.649', '-0.1393', '0.3655', '0.8003', '-0.3057', '-0.3425', '0.003134', '-0.08344', '0.7476', '-0.14', '-0.325', '-0.714', '-0.5415', '-0.8306', '-0.7627', '-0.0977', '0.1178', '-0.05676', '-0.2462', '-0.2651', '0.1731', '-0.5273', '1.085', '-0.4539', '-0.3003', '-0.05582', '0.255', '0.3596', '0.371', '-0.1265', '-0.3113', '-0.56', '-0.5615', '-0.1067']",C4024,0005922,D000077277,,,,
mondo:0005581,AVL induced bursal lymphoma,,,,,,,,0005923,,,,,
mondo:0005582,binge eating disorder,['binge eating'],,,,,,C97162,0005924,D002032,,,,
mondo:0005583,non-human animal disease,"['animal disease', 'diseases, animal']",,,,C0003047,,,0005932,D000820,,,,
mondo:0005584,congenital left-sided heart lesions,,,,,,"['-0.165', '0.0594', '0.1643', '-0.01881', '0.2786', '-0.2537', '0.1575', '0.2428', '-0.1406', '-0.1793', '-0.2656', '-0.329', '-0.01186', '0.2236', '-0.462', '-0.2666', '-0.4556', '-0.08044', '-0.2235', '-0.4941', '0.11993', '0.2893', '0.1934', '-0.2152', '0.05075', '-0.01794', '0.04422', '0.26', '0.3477', '0.05862', '0.264', '-0.0849', '0.2795', '0.2252', '0.0792', '-0.287', '0.2568', '0.03198', '0.1434', '-0.2754', '0.0851', '0.11206', '0.2113', '0.0744', '0.01996', '0.04507', '-0.02994', '0.3953', '-0.2075', '0.0846', '-0.11584', '0.1477', '0.1934', '-0.08594', '-0.2328', '-0.11786', '0.1131', '0.06464', '-0.174', '-0.0827', '0.05914', '0.2715', '-0.258', '0.0725', '-0.04', '-0.1464', '0.3281', '0.3774', '-0.4604', '0.1868', '-0.1486', '0.06152', '0.1246', '-0.1704', '-0.2404', '-0.02705', '-0.02083', '-0.1512', '-0.2615', '-0.2732', '-0.131', '0.005875', '-0.005955', '0.1603', '-0.0875', '-0.1009', '0.2396', '0.00688', '-0.001604', '-0.142', '0.0059', '0.0508', '0.1992', '0.1459', '0.645', '0.02974', '0.4048', '-0.1451', '-0.0632', '0.1603']",,0005938,,,,,
mondo:0005585,chemotherapy-induced hypertension,,,,,,,,0005942,,,,,
mondo:0005586,head and neck neoplasm,"['tumour of craniocervical region', 'head and neck neoplasm', 'tumor of craniocervical region', 'tumor of head and neck', 'craniocervical region tumour', 'craniocervical region neoplasm (disease)', 'neoplasm of head and neck', 'tumour of head and neck', 'neoplasm of the head and neck', 'tumour of the head and neck', 'craniocervical region tumor', 'head and neck tumour', 'head and neck tumor', 'neoplasm of craniocervical region', 'head and neck neoplasm (excluding central nervous system)', 'tumor of the head and neck']",,,,C0018671,,C3077,0005950,,239.89,,,
mondo:0005588,chemotherapy-induced oral mucositis,,,,,,,,0006313,,,,,
mondo:0005589,thiopurine immunosuppressant-induced pancreatitis,,,,,,,,0006315,,,,,
mondo:0005590,breast ductal adenocarcinoma,"['ductal breast adenocarcinoma', 'breast ductal carcinoma', 'duct carcinoma', 'mammary duct adenocarcinoma', 'ductal carcinoma of the breast', 'duct adenocarcinoma', 'ductal adenocarcinoma', 'ductal carcinoma of breast', 'ductal breast carcinoma', 'ductal carcinoma']",3007,,,,,C4017,0006318,D018270,,,,
mondo:0005591,pit and fissure surface dental caries,,,,,,,,0006338,,521.06,,,
mondo:0005592,smooth surface dental caries,,,,,,,,0006339,,521.07,,,
mondo:0005593,chronic periodontitis,"['periodontitis, chronic']",,,,,"['0.925', '-0.2338', '0.2161', '0.6846', '0.479', '-0.552', '0.1268', '0.4548', '-0.558', '0.869', '-0.4092', '-0.521', '-0.3906', '0.9053', '-0.1793', '-0.1005', '-0.52', '0.5386', '-0.4673', '-1.335', '-0.12085', '-0.3481', '0.2021', '-0.4634', '-0.2186', '-0.6323', '-0.953', '0.02411', '0.1476', '-0.2257', '-0.424', '0.3145', '-0.152', '0.3286', '0.8228', '0.902', '0.07007', '0.188', '0.7666', '-0.846', '0.1164', '0.248', '-0.4746', '-0.0735', '0.2186', '0.12134', '-0.2124', '-0.0768', '-0.0705', '-0.273', '-0.0217', '0.2386', '0.459', '0.0823', '-0.496', '-0.4634', '-0.4275', '-0.0668', '-1.333', '-0.9414', '-0.3296', '0.1792', '-0.283', '-0.4963', '-0.4639', '0.187', '0.6436', '0.008606', '0.0654', '1.147', '0.1909', '-0.1069', '0.564', '-0.955', '0.735', '0.2441', '-0.1636', '0.5527', '-0.3015', '-0.4602', '-0.8833', '-0.3186', '-0.0829', '0.127', '0.5566', '0.0419', '0.2435', '-0.29', '0.802', '0.02191', '0.3555', '0.2175', '0.2966', '0.63', '0.1886', '0.1355', '-0.4646', '-1.102', '-0.3823', '-0.003536']",C35326,0006343,D055113,523.40,K05.3,,
mondo:0005594,severe cutaneous adverse reaction,"['SCAR', 'scarring', 'Scar']",,,,,,C34483,0006346,,,,20000020,
mondo:0005595,laryngeal squamous cell carcinoma,"['squamous cell carcinoma of the larynx', 'LXSC', 'epidermoid carcinoma of larynx', 'larynx epidermoid carcinoma', 'larynx squamous cell carcinoma', 'epidermoid carcinoma of the larynx', 'squamous cell carcinoma of larynx', 'laryngeal throat squamous cell cancer', 'laryngeal squamous cell carcinoma', 'laryngeal epidermoid carcinoma']",2876,,494550,C0280324,,C4044,0006352,,,,,
mondo:0005596,cystadenocarcinoma,"['cystadenocarcinoma (morphologic abnormality)', 'cystadenocarcinoma', 'cystadenocarcinoma, malignant', 'cystadenocarcinoma NOS (morphologic abnormality)']",3111,,,C0010631,,C2971,0006387,D003536,,,,
mondo:0005597,cystic renal cell carcinoma,,,,,,,,0006388,,,,,
mondo:0005598,dopaminergic neuroblastoma,,,,,,,,0006391,,,,,
mondo:0005599,malignant epithelioid mesothelioma,"['epithelioid mesothelioma', 'epithelial mesothelioma', 'epithelioid mesothelioma, malignant', 'epithelioid mesothelioma, malignant (morphologic abnormality)', 'malignant epithelial mesothelioma']",4489,,,C0862312,,C7985,0006452,,,,,
mondo:0005601,ovarian mucinous adenocarcinoma,"['mucinous adenocarcinoma of the ovary', 'ovarian mucinous carcinoma', 'mucinous carcinoma of ovary', 'ovary mucinous adenocarcinoma', 'mucinous carcinoma of the ovary', 'mucinous adenocarcinoma of ovary', 'ovarian mucinous adenocarcinoma']",3606,,398961,CN205033,,C5243,0006462,,,,,
mondo:0005602,ovarian teratoma,"['ovarian teratoma', 'teratoma of ovary', 'germ cell teratoma of the ovary', 'germ cell teratoma of ovary', 'teratoma of the ovary', 'ovarian germ cell teratoma']",5567,,,C0280131,,C8110,0006463,,,,,
mondo:0005603,pancreatic tubular adenocarcinoma,['pancreas tubular adenocarcinoma'],,,,,,,0006471,,,,,
mondo:0005605,transitional cell papilloma,"['transitional cell papilloma', 'transitional cell papilloma, benign (morphologic abnormality)', 'papilloma, transitional cell, benign', 'transitional papilloma', 'transitional cell papilloma NOS (morphologic abnormality)', 'transitional cell papilloma, benign']",2670,,,C0334266,,C4115,0006497,,,,,
mondo:0005606,tubular adenocarcinoma,"['tubular carcinoma', 'tubular adenocarcinoma (morphologic abnormality)', 'tubular adenocarcinoma', 'carcinoma, tubular cell, malignant']",4929,,,C0205645,,C65192,0006500,,,,,
mondo:0005607,chronic bronchitis,"['bronchitis, chronic']",,,,C0008677,,C26722,0006505,D029481,491.9,,,
mondo:0005608,varicella zoster infection,"['Varicella-zoster Virus infection', 'varicella zoster infection']",,,,C0586989,,C96407,0006509,,052.7,,,
mondo:0005609,herpes zoster,"['shingles', 'Zoster', 'herpes Zoster', 'herpes zona']",8536,,,C0019360,,C71079,0006510,D006562,053,B02,,
mondo:0005610,Kashin-Beck disease,,,,,C2745963,,,0006511,D057767,716.08,,,
mondo:0005611,bladder transitional cell carcinoma,"['transitional cell carcinoma of bladder', 'bladder urothelial cancer', 'urothelial carcinoma of the urinary bladder', 'BLCA', 'urinary bladder transitional cell carcinoma', 'bladder urothelial carcinoma', 'urinary bladder urothelial carcinoma', 'transitional cell carcinoma of the urinary bladder', 'bladder transitional cell carcinoma', 'urothelial bladder carcinoma']",4006,,,C0279680,,C39851,0006544,,,,,
mondo:0005613,mesonephric adenocarcinoma,['malignant mesonephroma'],,,,,,C4072,0006719,,,,,
mondo:0005614,pancreatic adenosquamous carcinoma,"['pancreatic mixed squamous and adenocarcinoma', 'adenosquamous carcinoma of the pancreas', 'PAASC', 'pancreatic adenosquamous cancer', 'pancreatic adenosquamous carcinoma', 'adenosquamous carcinoma of pancreas', 'pancreatic adenoacanthoma', 'pancreatic mucoepidermoid carcinoma', 'pancreas adenosquamous carcinoma', 'adenosquamous pancreas carcinoma']",5637,,,C1335299,,C5721,0006732,,,,,
mondo:0005615,plasmacytoma,"['anaplastic solitary extramedullary plasmacytoma of the cecum (type)', 'solitary plasmacytoma', 'anaplastic plasmacytoma', 'plasmacytoma', 'anaplastic skeletal plasmacytoma (type)', 'solitary myeloma', 'extramedullary anaplastic plasmacytoma (type)', 'myeloma - solitary', 'myeloma, solitary']",3721,,86855,C0032131,,C9349,0006738,D010954,238.6,,10035484,
mondo:0005616,pulmonary mucoepidermoid carcinoma,"['lung mucoepidermoid cancer', 'lung mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the lung']",0050932,,,C1708778,,C45544,0006740,,,,,
mondo:0005617,undifferentiated carcinoma,"['carcinoma, undifferentiated', 'carcinoma, undifferentiated, malignant', 'undifferentiated carcinoma', 'anaplastic carcinoma']",,,,C0205698,,C3692,0006772,,,,,
mondo:0005618,anxiety disorder,"['anxiety state', 'anxiety', 'anxiety disorder']",2030,,,,,C2878,0006788,D001008,300.09,,,
mondo:0005619,typhoid fever,"['typhoid', 'typhoid fever', 'typhoidal salmonellosis']",13258,,99745,C0041466,,C35089,0006789,D014435,002.0,,,
mondo:0005620,cerebral amyloid angiopathy,"['CAA, familial', 'dutch hereditary cerebral amyloid angiopathy', 'cerebral amyloid angiopathy, familial', 'cerebral amyloid angiopathy, genetic', 'HCHWA', 'hereditary cerebral haemorrhage with amyloidosis - Dutch type', 'hereditary cerebral hemorrhage with amyloidosis - Dutch type']",9246,,85458,,"['-0.0202', '-0.0231', '-0.7407', '0.3604', '-0.4446', '-0.4438', '-0.3755', '0.0837', '-0.4954', '0.1572', '-0.6953', '-0.642', '0.04602', '-0.287', '0.2844', '-0.2532', '-0.02733', '-0.2502', '-0.02419', '-0.3345', '1.03', '-0.1233', '0.627', '0.2524', '-0.2795', '-0.1517', '-0.58', '-0.0435', '-0.3706', '0.5684', '0.564', '-0.294', '0.9614', '-0.1192', '0.3223', '-0.3267', '-0.0889', '-0.261', '-0.04285', '-0.3228', '1.332', '-0.8984', '0.611', '-0.2435', '0.4524', '0.528', '-0.4785', '-0.631', '0.478', '-0.1782', '0.354', '0.726', '0.3442', '-0.4175', '-0.02054', '0.0985', '0.73', '0.00441', '-0.5024', '0.6953', '-0.393', '0.03946', '0.3555', '-0.636', '-0.198', '0.3762', '0.2634', '0.3792', '-0.76', '0.4917', '0.1138', '-0.0831', '0.1417', '-0.269', '0.6167', '0.619', '0.2009', '0.303', '-0.12354', '-0.18', '-0.4336', '-0.39', '-0.3284', '0.07135', '0.37', '0.1771', '0.576', '0.7886', '0.126', '-0.1685', '0.2708', '-0.324', '-0.1562', '-0.6807', '0.4856', '0.7944', '0.1544', '-0.09607', '-0.02278', '-0.01595']",C84625,0006790,D016657,277.39,I68.0,,
mondo:0005621,vascular brain injury,"['Vascular Brain injury', 'Brain Vascular trauma', 'injury, Brain Vascular', 'trauma, Brain Vascular', 'Brain injury, Vascular', 'Vascular trauma, Brain', 'trauma, cerebrovascular', 'Vascular Brain Injuries', 'Vascular injury, Brain', 'injury, Vascular Brain', 'injury, Vascular, Brain', 'Vascular Traumas, Brain', 'Brain Vascular injury']",,,,,,,0006791,D020214,,,,
mondo:0005623,autoimmune thyroid disease,"['thyroiditides, autoimmune', 'thyroiditides, lymphomatous', 'autoimmune thyroiditides', 'thyroiditis, lymphocytic', 'autoimmune thyroiditis', 'lymphocytic thyroiditides', 'lymphocytic thyroiditis', 'thyroiditides, lymphocytic', 'thyroiditis, lymphomatous', 'lymphomatous thyroiditides', 'lymphomatous thyroiditis']",,,,,,,0006812,D013967,,,,
mondo:0005624,atrophic thyroiditis,,,,,C0238183,,,0006813,,,,,
mondo:0005625,cerebral malaria,['malarial encephalitis'],14069,,,C0024534,,C128373,0006857,D016779,084.9,,,
mondo:0005626,epithelial neoplasm,"['epithelioma', 'epithelial neoplasm']",,,,,,C3709,0006858,D009375,,,,
mondo:0005627,head and neck cancer,"['malignant tumor of head and neck', 'head and neck tumours', 'malignant neoplasm of craniocervical region', 'head and neck neoplasm', 'tumour of head and neck', 'malignant head and neck neoplasm', 'malignant craniocervical region neoplasm', 'malignant neoplasm of the head and neck', 'cancer of head and neck', 'malignant tumor of the head and neck', 'malignant neoplasm of head and neck', 'head and neck malignant neoplasia', 'malignant head and neck tumour', 'cancer of craniocervical region', 'cancer of the head and neck', 'head and neck cancer', 'craniocervical region cancer', 'malignant tumour of the head and neck', 'head/neck neoplasm', 'head and neck tumors', 'malignant head and neck tumor', 'malignant tumour of head and neck']",11934,,,C0278996,,C4013,0006859,,,,,
mondo:0005628,male breast carcinoma,"['carcinoma of the Male breast', 'male breast carcinoma', 'malignant neoplasm of male breast', 'male breast cancer', 'breast cancer in men', 'Male breast carcinoma', 'neoplasm of male breast', 'breast cancer, male', 'Male breast cancer', 'carcinoma of male breast', 'carcinoma of Male breast']",1614,,,C0242788,,C3862,0006861,D018567,175.9,,,
mondo:0005629,Acanthamoeba keratitis,"['keratitis, Acanthamoeba', 'Acanthamoeba caused keratitis']",,,67043,C0000880,,C50450,0007126,D015823,370.8,,10069408,
mondo:0005630,actinobacillosis,,4974,,,C0001247,,,0007127,D000187,,,,
mondo:0005631,actinomycosis,"['Actinomycetes', 'actinomycetoma', 'actinomycotic madura foot', 'Keratoactinomycosis', 'actinomycotic mycetoma of foot', 'Actinomyces infection', 'Actinomyces israeli', 'actinomycotic mycetema', 'infections, Actinomyces', 'boil', 'anaerobic Actinomyces infection', 'Madura foot due to Actinomadura', 'canaliculitis']",8478,,457095,C0001261,,C34350,0007128,D000196,039.9,,,
mondo:0005632,acute chest syndrome,"['ACS', 'acute chest syndrome in sickle cell disease']",1584,,,C0742343,,C138179,0007129,D056586,517.3,,,
mondo:0005634,acute hemorrhagic conjunctivitis,"['epidemic hemorrhagic conjunctivitis', 'Apollo disease', 'viral conjunctivitis']",11227,,,C0009765,,C34505,0007131,D003232,077.4,,,
mondo:0005635,adenomyoma,"['adenomyoma, benign', 'adenomyoma', 'adenomyoma (morphologic abnormality)']",2609,,,C0206622,,C3726,0007133,D018194,,,,
mondo:0005636,adenosarcoma,"['Mullerian adenosarcoma', 'Müllerian adenosarcoma', 'mullerian adenosarcoma', 'adenosarcoma (morphologic abnormality)', 'adenosarcoma']",1974,,,C0001442,,C9474,0007134,D018195,,,,
mondo:0005638,agnosia,"['dyspraxia (finding)', 'agnosia', 'visual amnesia', 'primary visual agnosia', 'Monomodal visual amnesia', 'dyspraxia syndrome']",4090,,,,,C84542,0007136,D001072,,R48.2,,
mondo:0005639,AIDS related complex,,,,,C0001857,,,0007137,D000386,,,,
mondo:0005640,akinetic mutism,"['Coma vigilans (finding)', 'Coma vigilans']",4267,,,C0001889,,,0007138,D000405,,,,
mondo:0005641,aleutian mink disease,"['Aleutian mink disease virus caused disease or disorder', 'Aleutian disease']",2934,,,C0002016,,,0007139,D000453,079.89,,,
mondo:0005642,atopic conjunctivitis,"['Atopic conjunctivitis', 'allergic conjunctivitis', 'allergic form of conjunctivitis (disease)']",11204,,,C0009766,,C34506,0007141,,372.14,,,0007879
mondo:0005643,Alphavirus infectious disease,['Alphavirus caused disease or disorder'],,,,C0206752,,,0007142,D018354,,,,
mondo:0005644,amebiasis,"['amoebiasis', 'entamoebiasis', 'chronic intestinal amebiasis']",9181,,,C0002438,,C84551,0007144,D000562,006.9,,,
mondo:0005645,ancylostomiasis,"['hookworm infection', 'Ancylostoma duodenale infection', 'Ancylostoma caused disease or disorder']",12841,,78,C0002831,,C35805,0007145,D000724,126.9,B76.1,10020376,
mondo:0005647,anogenital human papillomavirus infection,"['genital Warts', 'anogenital Human papilloma Virus infection', 'anogenital Human Papillomavirus infection', 'anogenital Human papilloma Virus infectious disease', 'condyloma acuminatum', 'venereal wart', 'anogenital Warts', 'genital wart virus infectious disease', 'anogenital venereal wart']",11168,,,,,C4820,0007147,D003218,078.11,,,
mondo:0005648,aortic valve insufficiency,"['rheumatic aortic valve insufficiency', 'rheumatic aortic valve regurgitation', 'aortic regurgitation', 'Corrigan^s disease', 'aortic incompetence', 'rheumatic aortic insufficiency', 'rheumatic aortic regurgitation', 'aortic insufficiency']",57,,,C0155568,,C51223,0007148,D001022,396.3,I06.1,,
mondo:0005649,appendicitis,"['vermiform appendix inflammation', 'acute appendicitis with peritoneal abscess', 'acute appendicitis with generalised peritonitis', 'acute appendicitis with generalized peritonitis', 'acute appendicitis']",8337,,,C0003615,,C35145,0007149,D001064,541,,,
mondo:0005650,Arenaviridae infectious disease,"['Arenaviridae infection', 'arenavirus infectious disease', 'arenavirus infections', 'Arenaviridae caused disease or disorder', 'arenavirus infection', 'infection, Arenaviridae', 'infections, arenavirus', 'infections, Arenaviridae', 'infection, arenavirus']",3944,,,,,,0007150,D001117,078.89,,,
mondo:0005651,arenavirus hemorrhagic fever,,,,,C0153112,,,0007151,,078.7,,,
mondo:0005652,Arterivirus infectious disease,['Arterivirus caused disease or disorder'],,,,C0206604,,,0007152,D018174,,,,
mondo:0005654,ascariasis,"['ascariasis - roundworm', 'Ascaris lumbricoides infection', 'Ascaris lumbricoides caused disease or disorder']",456,,,C0003950,,C128392,0007154,D001196,127.0,B77,,
mondo:0005655,ascaridiasis,['Ascaridia caused disease or disorder'],3108,,,C0003952,,,0007155,D001198,,B77,,
mondo:0005656,Ascaridida infectious disease,"['infections, Ascaridida', 'Ascaridida infection', 'Ascaridida caused disease or disorder', 'infection, Ascaridida']",,,,,,,0007156,D017191,,,,
mondo:0005657,aspergillosis,['infection due to Aspergillus'],13564,,1163,C0004030,,C2886,0007157,D001228,117.3,B44,10003488,
mondo:0005658,Astroviridae infectious disease,,,,,C0376550,,,0007158,D019350,,,,
mondo:0005659,atrophic rhinitis,"['rhinitis, atrophic', 'ozena', 'rhinitis sicca', 'Ozaena', 'dry rhinitis']",4731,,,C0035459,,,0007159,D012222,,,,
mondo:0005660,Avulavirus infectious disease,,,,,C1258034,,,0007161,D045463,,,,
mondo:0005661,babesiosis,"['babesiasis', 'piroplasmosis', 'Babesia parasite infection', 'Babesia caused disease or disorder', 'infection by Babesia', 'Human babesiosis']",9643,,108,C0004576,,C84581,0007162,D001404,088.82,B60.0,10003965,
mondo:0005662,balantidiasis,"['Human balantidiasis', 'balantidiosis', 'B coli infection', 'large-intestinal infection with Balantidium coli', 'Balantidiases', 'Balantidium coli infection', 'ciliary dysentery']",12386,,1223,C0004692,,C84583,0007163,D001447,007.0,A07.0,10004080,
mondo:0005663,Barre-Lieou syndrome,"['posterior cervical sympathetic syndrome', 'Cervicocranial syndrome']",6692,,,C2355645,,C34411,0007165,D055010,723.2,M53.0,,
mondo:0005664,bartonellosis,"['Bartonella infection', 'Rochalimaea infection', 'Bartonella infectious disease', 'bartonelliasis', 'Rochalimaea infections', 'Bartonella caused disease or disorder', 'Rochalimaea infection (disorder)']",11102,,,C0004771,,C84586,0007166,D001474,088.0,A44,,
mondo:0005665,Bell^s palsy,"['facial palsy', 'nerve paralysis, Facial', 'Bell^s (facial) palsy', 'palsy of facial nerve', 'Bell palsy', 'paralysis Of Facial nerve', 'facial nerve palsy', 'facial nerve paralysis']",12506,,2810,C0376175,,C26769,0007167,D020330,351.0,G51.0,,
mondo:0005667,biliary dyskinesia,['sphincter of Oddi dysfunction'],4140,,,C0005416,,,0007169,D001657,575.8,,,0012396
mondo:0005668,bird fancier^s lung,"['pigeon-breeder lung disease', 'bird breeder^s lung', 'bird fancier^s lung', 'pigeon breeder^s lung', 'Avian hypersensitivity pneumonitis', 'bird fancier lung', 'bird-fancier^s lung', 'bird-fanciers^ lung', 'bird-breeder^s lung', 'pigeon-breeder^s lung', 'poultry worker^s lung']",13891,,99908,C0005592,,C34425,0007170,D001716,495.2,J67.2,10004941,
mondo:0005669,black piedra,,12711,,,C0153249,,,0007171,,111.3,B36.3,,
mondo:0005670,blackwater fever,"['Black water fever', 'malarial hemoglobinuria', 'blackwater fever', 'hemoglobinuric, malaria']",14068,,,C0005681,,C34426,0007172,D001742,084.8,,,
mondo:0005671,Blastocystis infectious disease,"['Blastocystis infection', 'infections, Blastocystis', 'infection, Blastocystis']",,,,,,,0007173,D016776,,,,
mondo:0005672,blastomycosis,"['Chicago disease', 'Gilchrist^s disease', 'Blastomyces dermatitidis caused disease or disorder', 'infection by Blastomyces dermatitidis', 'blastomycotic infection', 'Blastomyces dermatitidis infection', 'North American blastomycosis']",12663,,,C0005717,,C34429,0007174,D001759,116.0,B40,,
mondo:0005673,blind loop syndrome,"['blind loop syndrome', 'bacterial overgrowth syndrome', 'stasis syndrome', 'stasis (blind loop) syndrome']",10606,,,C0005750,,C34431,0007175,D001765,579.2,,,
mondo:0005674,bone giant cell tumor,"['giant cell neoplasm of bone', 'giant cell tumor, benign', 'giant cell tumour of bone NOS (morphologic abnormality)', 'giant cell tumor of the bone', 'benign bone giant cell tumor', 'giant cell tumour of bone', 'giant cell tumour of the bone', 'benign bone giant cell tumour', 'giant cell tumor of bone', 'Osteoclastoma, benign', 'giant cell tumor of bone NOS (morphologic abnormality)', 'giant cell tumour of bone (morphologic abnormality)', 'giant cell myeloma', 'osteoclastoma', 'GCT of bone', 'giant cell tumor of bone (morphologic abnormality)']",4305,,363976,C0206638,,C121932,0007176,D018212,,,,0011847
mondo:0005675,border disease,,,,,C0006008,,,0007177,D001882,,,,
mondo:0005676,borna disease,['enzootic encephalomyelitis'],5154,,,C0006023,,,0007178,D001890,,,,
mondo:0005677,Rickettsia conorii infectious disease,,,,,,,,,,,,,
mondo:0005678,bovine respiratory disease complex,,,,,C1449809,,,0007180,D048090,,,,
mondo:0005679,bovine virus diarrhea-mucosal disease,"['bovine hemorrhagic syndrome', 'hemorrhagic syndrome, bovine']",5115,,,C0950112,,,0007181,D030243,,,,
mondo:0005680,Brill-Zinsser disease,"['recrudescent typhus', 'Brill^s disease', 'sporadic typhus', 'latent typhus', 'Brill Zinsser disease', 'Brill disease']",11254,,99990,C0006181,,,0007182,,081.1,,,
mondo:0005682,bronchopneumonia,"['chest infection - unspecified bronchopneumonia', 'lobular pneumonia', 'chest infection - bronchopneumonia', 'bronchial pneumonia']",12375,,,C0006285,,C26710,0007184,D001996,485,,,
mondo:0005683,brucellosis,"['Malta fever', 'Mediterranean fever', 'bang^s disease', 'Rock fever', 'Gibraltar fever', 'undulant fever', 'Maltese fever', 'Cyprus fever']",11077,,1304,C0006309,,C84602,0007185,D002006,023.9,A23,10006500,
mondo:0005684,bulbar polio,"['bulbar polio', 'bulbar poliomyelitis', 'polio, bulbar', 'medullary involvement poliomyelitis', 'poliomyelitis, medullary involvement']",9786,,,C0032372,,,0007186,D011052,045.0,,,
mondo:0005687,Caliciviridae infectious disease,"['Calicivirus infections', 'infection, Caliciviridae', 'infection, Calicivirus', 'Calicivirus infection', 'infections, Caliciviridae', 'Caliciviridae infection', 'infections, Calicivirus']",,,,,,,0007189,D017250,,,,
mondo:0005688,campylobacteriosis,,13622,,,C0006818,,,0007190,D002169,,,,
mondo:0005689,cannabis dependence,"['cannabis abuse', 'marijuana dependence', 'marijuana abuse']",9505,,,,,C34445,0007191,D002189,305.2,,,
mondo:0005690,Caplan syndrome,"['Caplan syndrome', 'Caplans syndrome', 'rheumatoid pneumoconiosis', 'Caplan^s disease', 'Caplan^s syndrome']",10326,,,C0006915,,,0007192,D002205,,,,
mondo:0005691,cardiovirus infectious disease,"['infection, Cardiovirus', 'Cardiovirus infection', 'infections, Cardiovirus']",,,,C0206617,,,0007194,D018188,,,,
mondo:0005692,cat-scratch disease,"['debre^s syndrome', 'debre-Mollaret syndrome', 'benign lymphoreticulosis', 'Cat-scratch fever', 'cat scratch fever', 'Foshay-Mollaret Cat scratch fever', 'bartonellosis due to Bartonella henselae infection', 'Cat scratch disease']",11258,,50839,CN205187,,C84620,0007195,D002372,078.3,A28.1,10007729,
mondo:0005693,cauda equina syndrome,"['cauda equina syndromic disease', 'syndromic disease of cauda equina']",11577,,,C0392548,,C35436,0007196,D011128,344.6,G83.4,,
mondo:0005694,cecal neoplasm,"['tumor of cecum', 'neoplasm of caecum', 'cecum tumour', 'tumour of cecum', 'caecum tumor', 'tumor of the cecum', 'tumour of the cecum', 'tumor of caecum', 'cecum neoplasm', 'cecum tumor', 'caecum neoplasm (disease)', 'neoplasm of cecum', 'cecal benign neoplasm', 'neoplasm of the cecum', 'tumour of caecum', 'caecum tumour']",1517,,,C0007528,,C4433,0007197,D002430,,,,
mondo:0005695,central nervous system AIDS arteritis,"['HIV-associated CNS Vasculitides', 'vasculitis of the central nervous system, HIV-associated', 'Vasculitides, HIV-associated CNS', 'vasculitis of the central nervous system, HIV associated', 'AIDS associated cerebral aneurysmal arteriopathy', 'CNS vasculitis, HIV-associated', 'HIV-associated vasculitis of the central nervous system', 'HIV-associated CNS vasculitis', 'CNS Vasculitides, HIV-associated', 'HIV-1-associated CNS Vasculitides', 'CNS vasculitis, HIV associated', 'AIDS-associated cerebral aneurysmal arteriopathy', 'HIV associated vasculitis of the central nervous system', 'HIV 1 associated CNS vasculitis', 'CNS vasculitis, HIV-1-associated', 'central nervous system AIDS arteritis', 'vasculitis, HIV-1-associated CNS', 'Vasculitides, HIV-1-associated CNS', 'cerebral aneurysmal arteriopathy, AIDS-associated', 'vasculitis, HIV-associated CNS', 'cerebral aneurysmal arteriopathy, AIDS associated', 'CNS Vasculitides, HIV-1-associated', 'HIV-1-associated CNS vasculitis']",,,,C0752331,,,0007198,D020943,,,,
mondo:0005696,central nervous system tuberculosis,"['tuberculosis of meninges and central nervous system', 'central nervous system tuberculosis', 'tuberculous abscess of brain', 'tuberculoma of brain', 'intracranial tuberculoma']",1638,,641396,C0275904,,,0007199,,013.35,,,
mondo:0005697,cerebral toxoplasmosis,"['Toxoplasma encephalitis', 'meningoencephalitis due to toxoplasmosis', 'encephalitis due to acquired toxoplasmosis']",10551,,,,,,0007200,D016781,130.0,,,
mondo:0005698,cervical incompetence,,9681,,,,,,0007202,D002581,654.50,,,
mondo:0005699,cervicofacial actinomycosis,"['cervicofacial actinomycotic infection', 'lumpy jaw']",,,,C0001264,,C34351,0007203,D000197,039.3,A42.2,,
mondo:0005700,chickenpox,"['varicella', 'chicken pox', 'Varicella', 'chickenpox', 'chicken pox infection']",8659,,,C0008049,,C97132,0007204,D002644,052.9,,,
mondo:0005701,chlamydia trachomatis infectious disease,"['chlamydia', 'Chlamydia trachomatis caused disease or disorder', 'Chlamydial infection', 'Chlamydia trachomatis infectious disease', 'chlamydial disease']",11263,,,,,C34463,0007205,D002690,079.98,,,
mondo:0005704,Ciliophora infectious disease,['Ciliophora caused disease or disorder'],,,,C0085308,,,0007209,D016770,,,,
mondo:0005705,clonorchiasis,['Oriental liver fluke disease'],13767,,,C0009021,,,0007210,D003003,121.1,B66.1,,
mondo:0005706,coccidioidomycosis,"['desert fever', 'desert rheumatism', 'Coccidioides immitis caused disease or disorder', 'Coccidioides infection', 'primary extrapulmonary coccidioidomycosis', 'Valley fever', 'California disease', 'San Joaquin valley fever']",13450,,228123,CN201384,,C84642,0007211,D003047,114.9,B38,10009825,
mondo:0005707,coccidiosis,"['coccidiosis (& [intestinal])', 'intestinal coccidiosis']",2113,,,C0009187,,C34493,0007212,D003048,007.2,,,
mondo:0005708,Colorado tick fever,"['Colorado tick fever virus caused disease or disorder', 'Colorado tick encephalitis', 'American mountain fever', 'Tick fever, American mountain', 'Colorado tick-borne disease', 'Mountain fever', 'Mountain tick fever']",4885,,83595,C0009400,,,0007213,D003121,066.1,A93.2,10010022,
mondo:0005709,common cold,"['acute nasopharyngitis', 'nasopharyngitis, acute', 'acute rhinitis', 'nasopharyngitis - acute', 'acute nasopharyngitis [common cold]', 'acute coryza', 'rhino-sinusitis', 'acute viral rhinopharyngitis']",10459,,,C0009443,,C34500,0007214,D003139,460,,,
mondo:0005710,composite lymphoma,"['composite lymphoma', 'composite Hodgkin and non-Hodgkin lymphoma']",5820,,168966,C1266191,,C38661,0007215,D058617,,,,
mondo:0005711,congenital diaphragmatic hernia,"['agenesis of hemidiaphragm', 'CDH', 'diaphragmatic hernia', 'unilateral agenesis of diaphragm', 'congenital diaphragmatic defect']",3827,,2140,C0235833,,C98893,0007216,D006551,,,10010439,
mondo:0005712,congenital nystagmus,"['congenital pathologic nystagmus', 'congenital idiopathic nystagmus', 'motor congenital nystagmus', 'nystagmus, congenital', 'nystagmus']",9649,,651,,,,0007217,D020417,379.51,H55.01,,0000639
mondo:0005714,congenital syphilis,"['mother-to-child transmission of syphilis', 'congenital syphilis', 'MTCT of syphilis']",9856,,499009,C0039131,,C84649,0007219,D013590,090.9,A50,,
mondo:0005715,congenital toxoplasmosis,"['mother-to-child transmission of toxoplasmosis', 'toxoplasmosis, congenital', 'toxoplasmosis - congen.', 'Toxoplasma embryopathy', 'Toxoplasma embryofetopathy', 'congenital toxoplasmosis']",13336,,858,C0040560,,C50503,0007220,D014125,771.2,P37.1,10010652,
mondo:0005716,contagious pleuropneumonia,,,,,C0032243,,,0007221,D011002,,,,
mondo:0005717,contagious pustular dermatitis,"['ecthyma, Contagious', 'thistle disease', 'ecthyma contagiosum', 'scabby mouth', 'sheep pox', 'Orf']",8771,,,C0013570,,,0007222,D004474,051.2,,,
mondo:0005718,Coronaviridae infectious disease,,,,,C0010078,,,0007223,,,,,
mondo:0005719,Coronavinae infectious disease,,,,,,,,0007224,D018352,,,,
mondo:0005720,cowpox,['yaba'],8956,,,C0010232,,,0007225,D015605,051.01,B08.010,,
mondo:0005721,coxsackievirus infectious disease,,10545,,,C0010246,,,0007226,D003384,,,,
mondo:0005722,croup,"['acute obstructive laryngitis', 'acute laryngotracheobronchitis', 'croup syndrome']",9395,,,C0010380,,C26735,0007227,D003440,464.4,,,
mondo:0005723,Cryptococcal meningitis,['Cryptococcus neoformans caused infectious meningitis'],0080159,,,,,C174113,0007228,D016919,321.0,,,
mondo:0005724,cryptococcosis,"['torulosis', 'Cryptococcal infection', 'European cryptococcosis', 'torula', 'cryptococcus neoformans infection', 'Cryptococcus neoformans caused disease or disorder', 'Busse-Buschke^s disease']",12053,,1546,C0010414,,C2967,0007229,D003453,117.5,B45,10011490,
mondo:0005725,cyclosporiasis,"['cyclosporosis', 'Cyclospora caused disease or disorder', 'Cyclospora cayetanensis caused disease or disorder', 'Cyclospora infection']",12750,,210,C4274225,,C128409,0007230,D021866,007.5,A07.4,,
mondo:0005728,diaphragm disorder,"['diaphragm disease or disorder', 'diaphragm disease', 'disorder of diaphragm', 'disease of diaphragm']",10481,,,C0152097,,,0007233,,519.4,,,
mondo:0005729,dicrocoeliasis,"['disease due to Dicrocoeliidae', 'Dicrocoelium caused disease or disorder']",1219,,,C1737210,,,0007234,D004011,121.8,,,
mondo:0005730,Dictyocaulus infectious disease,"['Dictyocaulus infection', 'infections, Dictyocaulus', 'Dictyocauliasis', 'infection, Dictyocaulus', 'Dictyocaulus caused disease or disorder', 'Dictyocauliases']",,,,C0012118,,,0007235,D004022,,,,
mondo:0005731,dipetalonemiasis,"['Dipetalonema infections', 'infection by Dipetalonema', 'Mansonella perstans', 'Dipetalonema infectious disease', 'Acanthocheilonemiasis', 'infection by Dipetalonema perstans', 'Dipetalonema infection', 'dipetalonemiasis', 'infection by Dipetalonema perstans (disorder) [ambiguous]', 'Mansonella perstans caused disease or disorder', 'Acanthocheilonema perstans infection']",14422,,,C0012517,,C34540,0007237,D004154,125.4,,,
mondo:0005734,dourine,,,,,C0013076,,,0007240,D004313,,,,
mondo:0005736,eastern equine encephalitis,"['Neuroinvasive Eastern equine encephalitis virus infection', 'Eastern equine encephalomyelitis', 'EEE']",10841,,83594,C0153065,,,0007242,D020242,062.2,A83.2,10014587,
mondo:0005737,Ebola hemorrhagic fever,"['EHF', 'Ebola fever', 'Ebola virus disease', 'Ebola', 'Ebolavirus caused disease or disorder']",4325,,319218,C0282687,,C36171,0007243,D019142,,,10014071,
mondo:0005738,echinococcosis,"['liver echinococcus', 'echinococcosis, unspecified, of liver', 'hydatid disease', 'echinococcosis of liver', 'pulmonary echinococcosis', 'hepatic echinococcosis', 'echinococcal disease', 'hydatidosis', 'Echinococcus caused disease or disorder']",1496,,,C0013502,,C84682,0007245,D004443,122.9,B67,,
mondo:0005739,echinostomiasis,"['Echinostomatoidea caused disease or disorder', 'infection by Echinochasmus']",1218,,,C0013514,,,0007246,D004451,121.8,,,
mondo:0005740,Echovirus infectious disease,"['infections, Echovirus', 'infection, echo Virus', 'Echovirus infection', 'infections, echo Virus', 'infection, Echovirus', 'Echovirus caused disease or disorder', 'echo Virus infections', 'echo Virus infection']",,,,C0013533,,,0007247,D004457,,,,
mondo:0005742,emphysematous cholecystitis,['gaseous pericholecystitis'],9765,,,C0521610,,C35592,0007249,D041882,,,,
mondo:0005743,encephalitozoonosis,['infection by Encephalitozoon'],4270,,,C0085412,,,0007250,D016890,136.8,,,
mondo:0005744,yolk sac tumor,"['infantile embryonal carcinoma', 'endodermal sinus tumor', 'yolk Sac tumor', 'endodermal sinus tumour', 'yolk Sac neoplasm', 'yolk sac tumor', 'yolk Sac tumor site unspecified', 'yolk Sac tumour site unspecified', 'endodermal sinus neoplasm', 'hepatoid yolk sac tumour', 'yolk SAC tumor, malignant', 'yolk Sac tumour', 'hepatoid yolk sac tumor']",1911,,876,C0014145,,C3011,0007252,,,,10048251,
mondo:0005745,Enoplea infectious disease,['Enoplea caused disease or disorder'],,,,,,,0007253,D017189,,,,
mondo:0005746,enterobiasis,"['threadworm infection', 'pinworm infection', 'Enterobius vermicularis caused disease or disorder', 'Enterobius vermicularis infection', 'Oxyuris vermicularis infection', 'oxyuriasis']",7457,,,C0086227,,C128396,0007254,D017229,127.4,B80,,
mondo:0005747,enterovirus infectious disease,"['Enterovirus infection', 'infections, Enterovirus', 'Enterovirus caused disease or disorder', 'infection, Enterovirus']",,,,C0014378,,,0007255,D004769,079.89,,,
mondo:0005748,enzootic pneumonia of calves,,,,,C0276046,,,0007256,D048089,,,,
mondo:0005749,eosinophilic pneumonia,"['pneumonia, eosinophilic', 'eosinophilic pneumonia']",5870,,,C1527407,,C35150,0007257,D011657,,,,
mondo:0005750,ephemeral fever,,,,,C0014481,,,0007258,D004810,,,,
mondo:0005751,epidemic pleurodynia,"['devil^s grip', 'Bornholm disease', 'Bamble disease', 'epidemic pleurisy', 'epidemic myalgia', 'epidemic, myositis']",10882,,,C0032238,,,0007259,D011000,074.1,B33.0,,
mondo:0005752,epidural abscess,"['intraspinal epidural abscess', 'spinal epidural abscess (disorder)', 'abscess epidural', 'intraspinal extradural abscess', 'spinal epidural abscess', 'spinal extradural abscess', 'extradural intraspinal abscess']",11387,,,C0270629,,,0007260,D020802,,,,
mondo:0005753,epiglottitis,"['mucosa of epiglottis inflammation', 'acute epiglottitis and supraglottitis', 'supraglottitis']",9398,,,C0014541,,C116007,0007261,D004826,464.3,,,
mondo:0005754,epilepsy with generalized tonic-clonic seizures,"['tonic-clonic epilepsy', 'grand Mal epilepsy', 'epileptic seizures, tonic-clonic']",7725,,,C0014549,,C3022,0007262,D004830,345.10,,,
mondo:0005755,equine infectious anemia,,,,,C0014661,,C84694,0007263,D004859,,,,
mondo:0005756,ethmoid sinusitis,"['sinusitis of ethmoid bone', 'ethmoidal sinusitis', 'ethmoiditis', 'ethmoid bone sinusitis']",9507,,,C0015029,,C34597,0007264,D015521,,,,
mondo:0005757,eumycotic mycetoma,"['maduromycosis', 'eumycetoma', 'mycotic mycetoma', 'Maduromycosis, mycotic', 'Madura foot']",13078,,,C0024449,,C85505,0007265,D008271,117.4,B47,,
mondo:0005758,eunuchism,"['Male hypergonadotropic hypogonadism', 'hypergonadotropic hypogonadism (Male)', 'Primary testicular failure']",5003,,,C0238117,,C131195,0007266,D005058,257.2,,,
mondo:0005759,fascioloidiasis,,1217,,,C0015655,,,0007268,D005213,,,,
mondo:0005761,filarial elephantiasis,"['Bancroftian elephantiasis', 'Malayi tropical eosinphilia', 'eyelid elephantiasis', 'elephantiasis', 'Bancroftian filarial chyluria', 'Wuchereriasis', 'Wuchereria Bancrofti infection', 'Bancroftian filariasis', 'elephantiasis of eyelid']",12211,,2035,,,C128360,0007272,D004605,374.83,,10016675,
mondo:0005762,Filoviridae infectious disease,['Filoviridae caused disease or disorder'],,,,C0242917,,,0007273,D018702,,,,
mondo:0005763,Flaviviridae infectious disease,['Flaviviridae caused disease or disorder'],,,,,,,0007274,D018178,,,,
mondo:0005764,follicular dendritic cell sarcoma,"['follicular dendritic cell sarcoma', 'follicular dendritic cell tumour', 'sarcoma of follicular dendritic cell', 'follicular Dendritic cell sarcoma', 'follicular dendritic cell tumor', 'follicular Dendritic cell sarcoma/tumor']",6262,,86902,C1260325,,C9281,0007276,D054740,,,,
mondo:0005765,foot and mouth disease,,,,,C0016514,,,0007277,D005536,,,,
mondo:0005766,fungal lung infectious disease,"['fungal disease, pulmonary', 'pulmonary fungal infection', 'fungal infection, pulmonary', 'pulmonary fungal disease', 'pulmonary fungal diseases', 'lung disease, fungal', 'fungal diseases, pulmonary', 'fungal lung diseases', 'fungal lung disease', 'fungal infections, pulmonary', 'pulmonary fungal infections', 'Fungi caused lung disease']",,,,C0024116,,,0007278,D008172,,,,
mondo:0005767,gas gangrene,"['gas gangrene', 'myonecrosis', 'gas bacillus infection']",9159,,,C0017105,,,0007279,D005738,040.0,A48.0,,
mondo:0005768,gastrointestinal tuberculosis,"['tuberculosis of gastrointestinal tract', 'tuberculosis of intestines, peritoneum and mesenteric glands', 'tuberculosis of intestines, peritoneum, and mesenteric glands']",404,,,C0152717,,,0007280,D014385,014.86,,,
mondo:0005769,geniculate herpes zoster,"['facial nerve palsy due to herpes zoster infection', 'geniculate neuralgia', 'facial nerve paralysis due to VZV', 'Ramsey Hunt syndrome', 'Herpes zoster auricularis', 'nervus intermedius neuralgia', 'Ramsay Hunt syndrome type II', 'facial nerve palsy due to VZV', 'Ramsay Hunt syndrome', 'Herpes Zoster Oticus', 'Hunt syndrome (formerly)', 'herpetic geniculate ganglionitis', 'Hunt^s syndrome (formerly)', 'Ramsay Hunt syndrome type 2 (formerly)', 'Ramsay Hunt syndrome type 2']",9210,,3020,C0458220,,C84763,0007281,,351.8,,,
mondo:0005770,genital herpes,"['herpes genitalis', 'genital herpes simplex', 'herpes genitalia', 'venereal herpes', 'virus-genital herpes']",8704,,,C0019342,,C14364,0007282,D006558,054.19,,,
mondo:0005771,geographic tongue,"['Pityriasis linguae', 'glossitis areata exfoliativa', 'benign migratory glossitis']",1455,,,C0017677,,C84588,0007283,,529.1,K14.1,,
mondo:0005772,geotrichosis,,2832,,,C0017455,,,0007284,D005847,117.9,B48.3,,
mondo:0005773,Gerstmann syndrome,"['developmental Gerstmann syndrome', 'aphasia-angular gyrus syndrome', 'Gerstmann tetrad', 'Gerstmann Badal syndrome', 'GS']",4969,,221117,,,,0007285,D005862,784.69,,10048608,
mondo:0005774,glanders,"['Burkholderia mallei', 'infection due to Pseudomonas mallei', 'Burkholderia mallei caused disease or disorder', 'Burkholderia mallei infection', 'farcy pipes']",13444,,,C0017589,,C34638,0007286,D005896,024,A24.0,,
mondo:0005775,G6PD deficiency,"['G-6-PD variant enzyme deficiency Anaemia', 'glucose-6-phosphate dehydrogenase deficiency', 'G-6-PD variant enzyme deficiency Anemia', 'G6PD', 'inborn error of glucose-6-phosphate dehydrogenase activity', 'rare inborn error of glucose-6-phosphate dehydrogenase activity', 'G6PD deficiency', 'glucosephosphate dehydrogenase deficiency', 'deficiency of G-6PD']",2862,,,C2939465,,C98933,0007287,D005955,,,,
mondo:0005776,gnathomiasis,"['Gnathostoma infection', 'Gnathostomiasis', 'infectious disease by Gnathostoma']",11379,,,C0018013,,C128395,0007289,D058429,128.1,B83.1,,
mondo:0005777,granuloma inguinale,"['granuloma inguinale', 'donovanosis', 'pudendal ulcer']",9113,,,C0018190,,C3065,0007291,D006100,099.2,A58,,
mondo:0005778,haemonchiasis,,3332,,,C0018477,,,0007293,D006188,,,,
mondo:0005779,"hand, foot and mouth disease","['vesicular stomatitis and exanthem', 'hand, foot, and mouth disease', 'HFMD', 'hand foot and mouth disease']",10881,,,C0018572,,C128439,0007294,D006232,074.3,,,
mondo:0005780,hantavirus infectious disease,"['infections, Hantavirus', 'Hantavirus caused disease or disorder', 'Hantavirus infection']",,,,C0242994,,C3899,0007295,D018778,079.81,,,
mondo:0005783,hemopericardium,"['haemopericardium', 'hemopericardium', 'hemopericardium (disease)']",11482,,,C0019064,,,0007298,,423.0,,,0011851
mondo:0005784,hantavirus hemorrhagic fever with renal syndrome,"['hemorrhagic fever, Russian', 'HFRS', 'hemorrhagic fever with renal syndrome', 'Puumala virus nephropathy', 'hemorrhagic nephrosonephritis']",11266,,,,,C84753,0007299,,078.6,A98.5,,
mondo:0005785,henipavirus infectious disease,['Henipavirus caused disease or disorder'],,,,,,,0007300,D045464,,,,
mondo:0005786,Hepadnaviridae infectious disease,['Hepadnaviridae caused disease or disorder'],,,,C0206746,,,0007301,D018347,,,,
mondo:0005787,hepatic tuberculosis,['tuberculosis of liver'],407,,,C0041313,,,0007302,D014386,017.90,,,
mondo:0005788,hepatitis E virus infection,"['hepatitis type E', 'Hepatitis E virus caused hepatitis']",4411,,,C0085293,,,0007303,D016751,,,,
mondo:0005789,hepatitis D virus infection,"['hepatitis type D', 'delta hepatitis', 'hepatitis delta', 'Hepatitis D virus', 'HDV', 'Hepatitis delta virus caused hepatitis']",2047,,402823,,,,0007304,D003699,070.52,,,
mondo:0005790,hepatitis A virus infection,"['hepatitis type A', 'viral hepatitis, type A', 'Hepatitis A', 'viral hepatitis A', 'Hepatitis A infection']",12549,,,C0019159,,C3096,0007305,D006506,,,,
mondo:0005791,herpangina,['vesicular pharyngitis'],10883,,,C0019338,,,0007306,D006557,074.0,,,
mondo:0005792,herpes simplex virus gingivostomatitis,"['Gingivostomatitides, herpetic', 'Simplexvirus caused stomatitis', 'herpetic Gingivostomatitis', 'simplex, oral Herpes', 'Gingivostomatitis, herpetic', 'Herpes simplex, oral', 'herpetic Gingivostomatitides', 'oral Herpes simplex', 'herpetic Stomatitides', 'Stomatitides, herpetic', 'herpetic stomatitis']",,,,,,,0007307,D013283,,,,
mondo:0005794,Herpesviridae infectious disease,"['infections, Herpesviridae', 'Herpesvirus infections', 'infection, Herpesvirus', 'Herpesviridae infection', 'infection, Herpesviridae', 'infections, Herpesvirus', 'Herpesviridae caused disease or disorder', 'Herpesviridae infections', 'Herpesvirus infection']",,,,,,,0007309,D006566,,,,
mondo:0005796,HIV enteropathy,,,,,C0282616,,,0007311,D019053,,,,
mondo:0005797,HIV wasting syndrome,,,,90081,C0343755,,,0007312,D019247,,,,
mondo:0005798,HIV-associated nephropathy,"['HIV nephropathy', 'AIDS-associated nephropathy', 'HIVAN', 'AIDS-related nephropathy']",,,,C0078911,,C26918,0007313,D016263,,,,
mondo:0005799,hookworm infectious disease,"['Bunostomiasis', 'infection, hookworm', 'hookworm infection', 'Bunostomiases', 'infections, hookworm']",,,,,,,0007314,,,,,
mondo:0005800,hordeolum,"['boil of eyelid', 'blepharitis of eyelid gland', 'furuncle of eyelid', 'Stye', 'eyelid gland blepharitis']",9909,,,C0019917,,C118722,0007315,D006726,,,,
mondo:0005801,human T-lymphotropic virus 1 infectious disease,"['HTLV-1', 'Human T-lymphotropic virus 1 caused disease or disorder', 'Human T lymphotropic virus type 1']",,,,C0020097,,,0007316,D015490,,,,
mondo:0005802,hymenolepiasis,"['Hymenolepsis infection', 'dwarf tapeworm infection', 'hymenolepiasis', 'Hymenolepis infectious disease']",10074,,401,C0277045,,C84768,0007317,D006925,123.6,B71.0,10020546,
mondo:0005803,hyperinsulinemic hypoglycemia,"['nesidioblastosis', 'persistent hyperinsulinemia hypoglycemia of infancy', 'islet cell hyperplasia', 'hyperinsulinemia hypoglycemia', 'hyperinsulinemic hypoglycemia (disease)']",13317,,443095,,,C4375,0007318,,,,,0000825
mondo:0005804,hyperprolactinemia,"['secretion, inappropriate prolactin', 'hyperprolactinemia', 'inappropriate secretion prolactin', 'inappropriate prolactin secretion syndrome', 'prolactin hypersecretion syndrome', 'hyperprolactinemias', 'inappropriate prolactin secretion', 'secretion prolactin, inappropriate', 'syndrome, prolactin hypersecretion', 'hyperprolactinemia (disease)', 'prolactin secretion, inappropriate', 'prolactin, inappropriate secretion', 'hyperprolactinaemia', 'hypersecretion syndrome, prolactin']",12700,,,C0020514,,,0007319,D006966,253.1,E22.1,,0000870
mondo:0005805,hypodermyiasis,['Oestridae caused disease or disorder'],12926,,430,C0020607,,,0007320,D007000,,,,
mondo:0005806,hypopharynx cancer,"['malignant neoplasm of other specified hypopharyngeal site', 'malignant hypopharyngeal tumor', 'hypural pharynx cancer', 'hypopharyngeal cancer', 'malignant neoplasm of hypopharynx', 'malignant tumor of the hypopharynx', 'malignant tumour of posterior wall of hypopharynx', 'pharynx cancer of hypopharynx', 'malignant neoplasm of other specified sites of hypopharynx', 'malignant hypopharyngeal tumour', 'malignant tumour of the hypopharynx', 'malignant tumor of posterior wall of hypopharynx', 'malignant tumour of hypopharynx', 'malignant neoplasm of posterior hypopharyngeal wall', 'malignant neoplasm of the hypopharynx', 'hypopharynx pharynx cancer', 'malignant hypopharyngeal neoplasm', 'malignant tumor of hypopharynx', 'malignant neoplasm of ill-defined sites within the lip and oral cavity', 'malignant neoplasm of posterior wall of hypopharynx']",8533,,,,,C7190,0007321,D007012,148.9,C13,,
mondo:0005807,idiopathic CD4-positive T-lymphocytopenia,,3109,,,C0206744,,C84780,0007322,D018344,,,,
mondo:0005808,inclusion conjunctivitis,"['adult inclusion conjunctivitis', 'Chlamydial conjunctivitis', 'inclusion blennorrhoea', 'inclusion blenorrhea', 'Paratrachoma', 'Trachoma', 'neonatal Chlamydia conjunctivitis']",13800,,,C0009770,,C116817,0007324,D003235,077.98,A74.0,,
mondo:0005809,infectious ectromelia,,,,,C0013591,,,0007325,D004482,,,,
mondo:0005810,infectious mononucleosis,"['monocytic angina', 'Mono', 'Filatov^s disease', 'mononucleosis', 'glandular fever', 'Gammaherpesviral mononucleosis', 'Pfeiffer^s disease']",8568,,,C0021345,,C34726,0007326,D007244,075,,,
mondo:0005811,infectious myxomatosis,,,,,C0027152,,,0007327,D009234,,,,
mondo:0005812,influenza,"['influenza with non-respiratory manifestation', 'influenza infection', 'flu', 'orthomyxoviridae caused disease or disorder', 'orthomyxoviridae infectious disease', 'Influenza with other manifestations']",8469,,,,,C53482,0007411,D009976,487.8,,,
mondo:0005813,interdigitating dendritic cell sarcoma,"['interdigitating cell sarcoma', 'interdigitating Dendritic cell sarcoma', 'interdigitating Dendritic cell sarcoma/tumor', 'interdigitating cell sarcoma/tumor']",7848,,,,,C9282,0007329,D054739,,,,
mondo:0005814,intestinal cancer,"['malignant intestinal tumours', 'intestinal tumors, malignant', 'bowel cancer', 'malignant tumor of the intestine', 'malignant intestinal neoplasms', 'intestinal cancer', 'malignant intestinal neoplasm', 'intestinal neoplasms, malignant', 'malignant intestinal tumors', 'malignant neoplasm of the intestine', 'malignant tumour of intestine', 'malignant intestine tumour', 'malignant intestine neoplasm', 'malignant tumor of intestine', 'malignant intestinal tumor', 'malignant tumour of the intestine', 'malignant neoplasm of intestine', 'cancer of intestine', 'malignant intestine tumor', 'cancer of the intestine', 'intestine cancer', 'malignant intestinal tumour']",10155,,,C0346627,,C4572,0007330,D007414,159.0,,,
mondo:0005815,pancreatic neuroendocrine neoplasm,"['Islet of Langerhans tumor', 'tumor of endocrine pancreas', 'neuroendocrine neoplasm of pancreas', 'neoplasm of endocrine pancreas', 'endocrine pancreas tumor', 'islet cell tumor', 'malignant tumour of endocrine pancreas', 'malignant pancreatic endocrine tumor', 'pancreatic NEN', 'tumour of endocrine pancreas', 'malignant pancreatic endocrine tumour', 'pancreatic endocrine neoplasm', 'malignant tumor of endocrine pancreas', 'islet cell tumour', 'pancreatic neuroendocrine neoplasm', 'endocrine pancreas tumour', 'PNEN', 'Islet cell tumors', 'endocrine pancreas neoplasm (disease)', 'Islet cell tumours', 'endocrine pancreas cancer', 'islet cell neoplasm', 'Islet of Langerhans tumour']",1799,,506052,,,C27031,0007331,,,,,
mondo:0005817,Kluver-Bucy syndrome,"['Klver-Bucy syndrome', 'Kluver Bucy syndrome', 'bilateral temporal lobe disorder', 'post-traumatic Kluver Bucy syndrome (type)', 'post-encephalitic Kluver Bucy syndrome (type)', 'memory loss, extreme sexual behavior, placidity, and visual distractibility', 'KLüver-Bucy syndrome', 'syndrome, Kluver-Bucy', 'temporal lobectomy behaviour syndrome', 'temporal lobectomy behavior syndrome']",2510,,157823,,,C84802,0007335,D020232,,,10066431,
mondo:0005819,laryngeal tuberculosis,"['tuberculous laryngitis', 'larynx tuberculosis']",1583,,,C0041315,,C26895,0007337,D014387,012.32,,,
mondo:0005820,Lassa fever,"['Lassa hemorrhagic fever', 'LF']",9537,,99824,C0023092,,C128418,0007338,D007835,078.89,A96.2,10023927,
mondo:0005821,late congenital syphilis,['juvenile neurosyphilis'],10039,,,,,,0007339,,090.7,,,
mondo:0005822,latent syphilis,,9531,,,C0039133,,C35056,0007340,D013592,097.1,,,
mondo:0005823,legionellosis,"['Legionella infection', 'Legionnaires disease']",10458,,600832,CN205282,,C128334,0007342,D007876,,,10061266,
mondo:0005824,Legionnaires^ disease,"['Legionella', 'infection by Legionella pneumophilia', 'Legionella pneumonia', 'legionnaire^s disease']",10457,,,,,C128339,0007343,D007877,482.84,,,
mondo:0005825,leptospirosis,"['hemorrhagic jaundice', 'spirochetal jaundice', 'Leptospira caused disease or disorder', 'rat catcher^s yellows', 'nanukayami fever', 'leptospirosis icterohaemorrhagica', 'Weil disease', 'cane-cutter fever', 'mud fever', 'rice-field fever', 'swamp fever', 'fort Bragg fever', 'Stuttgart disease', 'Icterohemorrhagic fever', 'canicola fever', 'swineherd^s disease']",2297,,509,C0023364,,C84825,0007344,D007922,100.9,A27,10024238,
mondo:0005826,lipid pneumonia,"['cholesterol pneumonia', 'exogenous lipoid pneumonia', 'pneumonia lipid', 'lipoidpneumonitis', 'lipoid pneumonitis']",3241,,,C0032298,,,0007345,D011017,,,,
mondo:0005827,lipoatrophic diabetes,"['lipoatrophic diabetes mellitus', 'diabete, lipoatrophic', 'lipoatrophic diabete', 'lipoatrophic diabetes', 'diabetes, lipoatrophic']",11712,,,,,C34537,0007346,D003923,,,,
mondo:0005828,listeriosis,"['Listeria monocytogenes caused disease or disorder', 'infection by Listeria monocytogenes', 'Listeria monocytogenes infection', 'Listeria infection']",11573,,533,C0023860,,C82994,0007347,D008088,027.0,A32,10024641,
mondo:0005829,louping ill,['Louping ill'],10250,,,C0024025,,,0007348,D008146,063.1,,,
mondo:0005830,lumpy skin disease,,,,,C0024106,,,0007349,D008166,,,,
mondo:0005831,lymph node tuberculosis,"['lymph node tuberculosis', 'scrofula', 'tuberculous adenitis', 'king^s evil', 'tuberculous lymphadenopathy']",4889,,,,,C26896,0007350,D014388,,,,
mondo:0005832,lymphangitis,['lymphatic vessel inflammation'],9317,,,C0024225,,C34790,0007351,D008205,457.2,I89.1,,
mondo:0005833,lymphatic system disorder,"['swollen glands', 'glands, swollen', 'lymphatic disease', 'swollen gland', 'lymphatic disorder', 'lympoid system disease', 'disorder of lymphatic part of lymphoid system', 'lymphadenopathy', 'adenopathy', 'disorder of lymphoid system', 'disorder of lymphatic system', 'lymphangiopathy', 'lymphatic part of lymphoid system disease', 'disease of lymphatic part of lymphoid system', 'disease of lympoid system', 'disorder of lymph node and lymphatics', 'lymphatic part of lymphoid system disease or disorder']",75,,,C0024228,,C50764,0007352,D008206,,,,
mondo:0005834,lymphogranuloma venereum,"['Poradenitis inguinale', 'lymphogranuloma inguinale', 'LGV', 'climatic or tropical bubo', 'Durand-Nicolas-Favre disease', 'lymph granuloma inguinale', 'strumous bubo']",13819,,,C0024286,,C26822,0007353,D008219,099.1,,,
mondo:0005835,Lynch syndrome,"['hereditary defective mismatch repair syndrome', 'familial non-polyposis colon cancer (hMSH2, hMLH1, hPMS1, hPMS2)', 'hereditary non-polyposis colon cancer type 1', 'HNPCC - hereditary nonpolyposis colon cancer', 'hereditary nonpolyposis colorectal cancer', 'Hereditary colorectal endometrial cancer syndrome', 'Hereditary non-polyposis colon cancer (hMSH2, hMLH1, hPMS1, hPMS2)', 'hereditary nonpolyposis colorectal neoplasm', 'Hereditary nonpolyposis colon cancer (hMSH2, hMLH1, hPMS1, hPMS2)']",3883,,144,C0009405,"['0.8267', '0.509', '-0.2329', '0.588', '-0.2323', '-0.1056', '0.02219', '0.7856', '-0.58', '-0.2018', '0.579', '0.2605', '-0.09924', '0.2018', '-0.2', '-0.863', '-0.322', '-0.4272', '-0.1915', '-0.5176', '-0.247', '-0.4902', '-0.1791', '-0.593', '0.628', '-0.3826', '-0.4666', '0.2957', '0.6675', '-0.04932', '0.754', '-0.4512', '0.3928', '-0.3423', '0.1614', '0.219', '-0.583', '0.3435', '-0.10944', '-0.5195', '0.3276', '-0.281', '0.06256', '-0.626', '-0.576', '-0.994', '-0.1137', '-0.4453', '0.53', '-0.1109', '-0.1316', '-0.205', '-0.4434', '-0.2424', '-0.2163', '-0.03934', '-0.3018', '1.335', '-0.512', '0.1962', '0.994', '-0.1294', '0.1653', '0.194', '0.05383', '0.7407', '0.10455', '0.7686', '-0.2766', '0.3542', '0.01037', '0.246', '-0.1153', '-0.01293', '0.4373', '-0.3267', '-0.603', '0.6167', '-0.1261', '-0.3354', '-0.02588', '0.5464', '0.1064', '0.345', '-0.352', '-0.266', '0.5454', '0.04626', '0.0759', '-0.2869', '-0.2341', '0.1259', '-0.5254', '-0.141', '0.69', '-0.429', '-0.009995', '-0.5254', '0.0921', '0.5796']",C8494,0007354,,,,10051981,
mondo:0005836,male reproductive organ cancer,"['neoplasm of male genital organ', 'malignant tumour of male reproductive system', 'tumor of male reproductive system', 'malignant tumor of the Male reproductive system', 'male reproductive organ cancer', 'malignant Male reproductive system tumour', 'malignant male reproductive organ neoplasm', 'malignant neoplasm of male genital organ or tract', 'male reproductive system neoplasm', 'malignant neoplasm of Male reproductive system', 'malignant Male reproductive system neoplasm', 'malignant neoplasm of male genital organs', 'malignant neoplasm of male genital organ', 'male genital cancer', 'malignant tumour of Male reproductive system', 'cancer of male reproductive organ', 'malignant tumour of the Male reproductive system', 'malignant tumour of male genital organ', 'male genital neoplasm', 'malignant tumor of Male reproductive system', 'tumour of male reproductive system', 'malignant neoplasm of male reproductive organ', 'malignant neoplasm of male genital organ, site unspecified', 'malignant Male reproductive system tumor', 'malignant tumor of male reproductive system', 'malignant tumor of male genital organ', 'malignant neoplasm of the Male reproductive system']",3856,,,,,C8561,0007355,D005834,187.9,,,
mondo:0005837,mandibular cancer,"['malignant neoplasm of lower jaw bone', 'cancer of mandible', 'mandibular neoplasm', 'malignant neoplasm of mandible', 'malignant neoplasm of inferior maxilla', 'mandible cancer', 'malignant mandible neoplasm', 'neoplasm of mandible']",2338,,,,,C35178,0007356,D008339,170.1,,,
mondo:0005838,mansonelliasis,"['Mansonellosis', 'Mansonella perstans infections']",1081,,2459,C0024759,,C84882,0007357,D008368,,B74.4,,
mondo:0005841,maxillary neoplasm,"['tumor of bone of upper jaw', 'maxillary cancer', 'maxillary neoplasm', 'bone of upper jaw tumour', 'bone of upper jaw tumor', 'tumour of bone of upper jaw', 'upper jaw bone cancer', 'bone of upper jaw neoplasm (disease)', 'neoplasm of bone of upper jaw']",4618,,,C0024954,,,0007360,D008441,,,,
mondo:0005842,maxillary sinusitis,,2051,,,C0024959,,C34809,0007361,D015523,,,,
mondo:0005843,mediastinal cancer,"['malignant neoplasm of the mediastinum', 'mediastinum cancer', 'cancer of mediastinum', 'tumour of mediastinum', 'malignant mediastinal neoplasm', 'malignant tumor of mediastinum', 'cancer of the mediastinum', 'malignant tumor of the mediastinum', 'mediastinal tumor', 'mediastinal cancer', 'malignant neoplasm of mediastinum', 'malignant tumour of mediastinum', 'malignant mediastinal tumour', 'malignant tumour of the mediastinum', 'malignant mediastinum neoplasm', 'mediastinal tumour', 'malignant mediastinal tumor', 'tumor of mediastinum']",5559,,,,,C3549,0007362,D008479,164.9,,,
mondo:0005844,chalazion,"['meibomian gland lipogranuloma', 'chalazion', 'chalazia', 'Meibomian cyst', 'cyst, Meibomian']",9903,,,C0007933,,C26717,0007363,D017043,373.2,H00.1,,
mondo:0005845,meningoencephalitis,,10554,,,C0025309,,C34813,0007364,D008590,,,,
mondo:0005846,microsporidiosis,"['infection by Microsporea', 'infection by Microspora', 'Microsporidiasis', 'infection by Microsporida', 'Microsporidia infection', 'Microsporidia caused disease or disorder']",4271,,2552,C0085407,,C84891,0007366,D016881,117.9,,10053982,
mondo:0005847,middle lobe syndrome,,2810,,,C0026069,,,0007367,D008878,,,,
mondo:0005848,miliary tuberculosis,"['generalized tuberculosis', 'disseminated tuberculosis', 'tuberculosis miliaris disseminata', 'generalised tuberculosis', 'acute miliary tuberculosis']",9861,,,C0152915,,C35086,0007368,D014391,018.90,A19,,
mondo:0005850,milker^s nodule,"['Pseudocowpox', 'Paravaccinia', 'milker nodule', 'milkers^ node']",8729,,,C0026143,,,0007370,D011213,051.9,,,
mondo:0005851,Miller Fisher syndrome,"['Guillain-Barre syndrome, Miller Fisher variant', 'Miller-Fisher syndrome', 'Fisher^s syndrome', 'Miller-Fisher variant of Guillain-Barre syndrome', 'Guillain Barre syndrome, Miller Fisher variant', 'cranial variant of Guillain-Barré syndrome', 'syndrome, Fisher', 'Fisher syndrome', 'cranial variant of GBS', 'Miller Fisher variant of Guillain Barre syndrome', 'syndrome, Miller-Fisher', 'syndrome, Miller Fisher', 'ophthalmoplegia, ataxia and areflexia syndrome', 'cranial variant of Guillain-Barre syndrome']",12889,,98919,C0393799,,C116958,0007371,D019846,,,10049567,
mondo:0005852,mitral valve stenosis,"['valve stenosis, mitral', 'valve stenoses, mitral', 'stenoses, mitral', 'mitral stenosis', 'stenoses, mitral valve', 'mitral stenoses', 'stenosis, mitral', 'mitral valve stenoses', 'stenosis, mitral valve']",1754,,,C0026269,,C50654,0007372,D008946,,,,
mondo:0005853,malignant mixed neoplasm,"['malignant mixed cancer', 'mixed tumor', 'malignant mixed tumours', 'mixed neoplasm, malignant', 'tumors, malignant mixed', 'malignant mixed tumour', 'tumor, malignant mixed', 'tumor, mixed, malignant', 'mixed tumor, malignant (morphologic abnormality)', 'mixed cell type cancer', 'mixed tumour', 'mixed neoplasm', 'malignant mixed tumor', 'malignant mixed neoplasm', 'mixed tumor, malignant', 'mixed tumor, malignant, NOS (morphologic abnormality)', 'mixed tumors, malignant', 'malignant mixed tumors']",154,,,C0206625,,C3729,1000356,D018198,,,,
mondo:0005854,mixed connective tissue disease,"['MCTD', 'sharp syndrome', 'mixed collagen vascular disease', 'connective tissue disease overlap syndrome']",3492,,809,C0026272,,C84892,0007374,D008947,,,10027754,
mondo:0005855,molluscum contagiosum,,8867,,,C0026393,,,0007375,D008976,078.0,B08.1,,
mondo:0005856,Mononegavirales infectious disease,['Mononegavirales caused disease or disorder'],,,,C0242916,,,0007376,D018701,,,,
mondo:0005857,morbillivirus infectious disease,['Morbillivirus caused disease or disorder'],,,,C0206614,,,0007377,D018185,,,,
mondo:0005858,mucinous cystadenocarcinoma,"['Pseudomucinous adenocarcinoma', 'mucinous cystadenocarcinoma NOS (morphologic abnormality)', 'mucinous cystadenocarcinoma (morphologic abnormality)', 'mucinous cystadenocarcinoma', 'Pseudomucinous cystadenocarcinoma']",3603,,,C0206699,,C3776,0007378,D018282,,,,
mondo:0005859,mucocutaneous leishmaniasis,"['mucocutaneous leishmaniasis, American', 'mucocutaneous leishmaniasis, (American)', 'American mucocutaneous leishmaniasis', 'cutaneous leishmaniasis, American', 'American cutaneous leishmaniasis', 'New World cutaneous leishmaniasis']",9155,,,C3495436,,C34769,0007379,D007897,085.5,B55.2,,
mondo:0005861,multidrug-resistant tuberculosis,"['multidrug-resistant TB', 'MDR-TB']",401,,,C0206526,,C128415,0007381,D018088,,,,
mondo:0005864,muscle cancer,"['malignant tumour of muscle', 'malignant muscle structure neoplasm', 'malignant tumour of the muscle', 'malignant neoplasm of muscle structure', 'malignant muscle tumor', 'malignant tumor of muscle', 'malignant neoplasm of muscle', 'malignant neoplasm of the muscle', 'malignant tumor of the muscle', 'malignant muscle neoplasm', 'muscle structure cancer', 'malignant muscle tumour', 'myosarcoma', 'cancer of muscle structure']",4045,,,C0684743,,C4883,0007384,,171.9,,,
mondo:0005865,mushroom workers^ lung,"['pholiota worker^s lung', 'pleurotus worker^s lung', 'bunashimeji worker^s lung', 'shimeji worker^s lung', 'mushroom workers lung', 'shiitaki worker^s lung']",2708,,,C0155889,,,0007385,,495.5,,,
mondo:0005866,mycobacterium avium complex disease,"['DMAC', 'Mycobacterium avium Complex', 'infection due to Mycobacterium intracellulare', 'Mycobacterium avium infection', 'disseminated infection with mycobacterium avium complex', 'Mycobacterium avium complex caused disease or disorder', 'MAC disease']",2755,,,C0026916,,C36197,0007386,D015270,031.8,,,
mondo:0005867,Mycoplasma pneumoniae pneumonia,"['Mycoplasma pneumonia', 'pneumonia due to Mycoplasma pneumoniae']",13276,,,,,C122526,0007387,D011019,483.0,,,
mondo:0005868,myelophthisic anemia,"['myelophthisis', 'leukoerythroblastic reaction', 'anemia, leukoerythroblastic', 'anaemia LEUKOERYTHROBLASTIC', 'leukoerythroblastosis', 'anemia LEUKOERYTHROBLASTIC']",2354,,,C0002890,,C36218,0007388,D000750,285.8,D61.82,,
mondo:0005870,necatoriasis,,2790,,,C0027528,,C34838,0007390,D009332,126.9,B76.1,,
mondo:0005871,Nematoda infectious disease,"['Infections, Nematode', 'Disease due to Nematoda', 'Nematoda caused disease or disorder', 'Nematode infection', 'Infection, Nematode', 'Nematodiasis', 'Nematode Infection', 'Nematode Infections']",,,,C0027583,,,0007391,D009349,,,,
mondo:0005872,nervous system cancer,"['malignant tumor of the nervous system', 'neural tumor', 'neural tumour', 'nervous system neoplasms, malignant', 'tumor of the nervous system', 'malignant tumour of the nervous system', 'malignant nervous system neoplasm', 'tumour of the nervous system', 'malignant nervous system tumor', 'nervous system cancer', 'cancer of nervous system', 'malignant tumor of nervous system', 'malignant tumour of nervous system', 'malignant neoplasm of nervous system', 'nervous system neoplasm', 'malignant nervous system tumour', 'malignant neoplasm of the nervous system', 'neural neoplasm']",3093,,,,,C4788,0007392,D009423,192.9,,,
mondo:0005873,neuroaspergillosis,,13565,,,C0752342,,,0007393,D020953,,,,
mondo:0005874,neuroschistosomiasis,,13722,,,C0752191,,,0007394,D020818,,,,
mondo:0005875,Newcastle disease,"['Newcastle^s disease', 'pseudo-fowlpest']",2929,,,C0027983,,C34849,0007395,D009521,,,,
mondo:0005876,Nidovirales infectious disease,['Nidovirales caused disease or disorder'],,,,C0969753,,,0007396,D030341,,,,
mondo:0005878,ocular onchocerciasis,"['onchocerciasis of eyeball of camera-type eye', 'eyeball of camera-type eye onchocerciasis']",,,,C0029002,,C34862,0007398,D015827,,,,
mondo:0005879,ocular toxoplasmosis,,,,,C0040561,,,0007399,D014126,130.7,,,
mondo:0005880,oesophagostomiasis,"['infection by Oesophagostomum', 'Oesophagostomum caused disease or disorder']",3983,,,C0028887,,,0007400,D009814,127.7,,,
mondo:0005881,oligohydramnios,"['antepartum oligohydramnios', 'oligohydramnios', 'delivered oligohydramnios', 'oligohydramnios (disease)', 'oligohydramnios - delivered']",12215,,,,,,0007401,D016104,658.00,,,0001562
mondo:0005883,ophthalmic herpes zoster,"['HZO', 'Herpes zoster ophthalmicus (HZO)']",,,,C0019364,,,0007403,D006563,053.29,,,
mondo:0005884,opisthorchiasis,"['infection by Opisthorchis', 'infection due to Opisthorchis (felineus)(viverrini)', 'infection due to cat liver fluke']",13768,,,C0029106,,,0007404,D009889,121.0,B66.0,,
mondo:0005885,optic neuritis,,1210,,,,,C84950,0007405,D009902,377.39,H46,,
mondo:0005886,oral candidiasis,"['thrush, oral', 'mouth candidiasis', 'oral moniliasis', 'candidiasis of mouth', 'thrush']",14262,,,C0006849,,C28137,0007406,D002180,112.0,,,
mondo:0005887,oral tuberculosis,,402,,,C0041323,,,0007407,D014393,528.9,,,
mondo:0005888,ornithosis,['psittacosis'],11262,,,C0029291,,C34873,0007410,D009956,073.9,,,
mondo:0005890,osteitis fibrosa,"['hyperparathyroid bone disease', 'osteitis fibrosa cystica generalisata', 'Von Recklinghausen^s disease of Bone', 'osteitis fibrosa cystica', 'Von Recklinghausen disease of Bone', 'Von Recklinghausen^s bone disease']",3341,,,C0029405,,C34875,0007413,D010002,,,,
mondo:0005891,ostertagiasis,,3985,,,C0029471,,,0007414,D010029,,,,
mondo:0005892,otitis media with effusion,"['secretory otitis Media', 'OME', 'serous otitis Media']",,,,,,C34886,0007415,D010034,381.29,,,
mondo:0005893,pancreatic endocrine carcinoma,"['pancreatic neuroendocrine carcinoma', 'islet cell carcinoma', 'pancreatic NEC', 'pancreatic endocrine cancer', 'endocrine pancreas carcinoma', 'carcinoma, islet cell, malignant', 'malignant pancreatic endocrine tumor', 'poorly-differentiated neuroendocrine neoplasm of pancreas', 'malignant pancreatic endocrine tumour', 'poorly-differentiated pancreatic NEN', 'poorly-differentiated NEN of pancreas', 'pancreatic endocrine carcinoma', 'islet cell cancer', 'malignant islet cell tumour', 'malignant islet cell tumor', 'high-grade pancreatic neuroendocrine carcinoma', 'carcinoma of endocrine pancreas', 'pancreatic NEC G3', 'malignant neoplasm of islets of Langerhans', 'high grade pancreatic neuroendocrine carcinoma', 'islet cell carcinoma (morphologic abnormality)', 'poorly-differentiated pancreatic neuroendocrine neoplasm', 'Pancreatic Neuroendocrine cancer', 'neuroendocrine carcinoma of pancreas', 'poorly differentiated pancreatic endocrine carcinoma']",1798,,506098,C1328479,,C3770,0007416,D018273,157.4,C25.4,,
mondo:0005894,paracoccidioidomycosis,"['South American blastomycosis', 'Lutz-Splendore-Almeida disease', 'mucocutaneous-lymphangitic paracoccidioidomycosis', 'lobo disease', 'Paracoccidioidal granuloma', 'PCM', 'paracoccidioidal mycosis']",12662,,73260,C0030409,,C34891,0007417,D010229,116.1,B41,10061906,
mondo:0005895,paragonimiasis,"['lung fluke infection', 'lung fluke disease', 'Paragonimus westermani caused disease or disorder', 'pulmonary paragonimiasis', 'infection by Paragonimus', 'Paragonimus westermani infection']",10699,,,C0030424,,C84995,0007418,D010237,121.2,B66.4,,
mondo:0005896,Paramyxoviridae infectious disease,['Paramyxoviridae caused disease or disorder'],,,,,,,0007419,D018184,,,,
mondo:0005898,paronychia,"['infected nailfold', 'paronychia (disease)', 'paronychia', 'onychia and paronychia of toe', 'paronychia inflammation', 'fungal nail infection', 'onychia and paronychia of finger']",13117,,,C0030578,,C79702,0007421,D010304,681.9,,,0001818
mondo:0005899,parotid disorder,"['disease of parotid gland', 'disorder of parotid gland', 'parotid gland disease', 'parotid gland disease or disorder']",10302,,,C0030579,,,0007422,D010305,,,,
mondo:0005900,parotitis,['parotid gland inflammation'],10301,,,C0030583,,C114281,0007423,D010309,,,,
mondo:0005901,pasteurellosis,"['Pasteurella caused disease or disorder', 'Pasteurella infectious disease', 'Pasteurella infection']",11055,,,C0030636,,,0007424,D010326,027.2,A28.0,,
mondo:0005903,pericardial tuberculosis,['tuberculous pericarditis'],4962,,,C0031049,,,0007426,D010495,017.90,,,
mondo:0005904,pericarditis,"['pericardium inflammation', 'pericarditis', 'pericarditis (disease)']",1787,,58208,C0031046,,C34915,0007427,D010493,,,,0001701
mondo:0005905,periodic limb movement disorder,['nocturnal myoclonus'],9207,,,C0751774,,,0007428,,327.51,G47.61,,
mondo:0005906,peritonsillar abscess,['quinsy'],,,,C0031157,,C128322,0007429,D000039,475,J36,,
mondo:0005907,persian gulf syndrome,['Gulf war syndrome'],4491,,,C0282550,,,0007430,D018923,300.89,,,
mondo:0005908,peste des petits ruminants infectious disease,"['Small ruminant morbillivirus caused disease or disorder', 'Peste des petits ruminants', 'Pseudorinderpest']",,,,C0949885,,,0007431,D029021,,,,
mondo:0005909,pestivirus infectious disease,"['Pestivirus caused disease or disorder', 'infections, Pestivirus', 'infection, Pestivirus', 'Pestivirus infection']",,,,C0206611,,,0007432,D018182,,,,
mondo:0005910,phagocyte bactericidal dysfunction,['phagocytic dysfunction'],3262,,,C0031306,,,0007433,D010585,,,,
mondo:0005911,pharyngoconjunctival fever,"['Adenoviral pharyngoconjunctivitis', 'pharyngoconjunctival fever', 'pharyngo-conjunctival fever']",13801,,,C0031351,,C34924,0007434,D000258,077.2,,,
mondo:0005912,phencyclidine abuse,"['PCP abuse', 'phencyclidine abuse']",5062,,,,,,0007436,D010623,305.90,,,
mondo:0005913,phlebotomus fever,"['Sandfly-borne Bunyavirus fever', 'Sandfly-borne phleboviral disease', 'pappataci fever', 'Sandfly fever', 'Sandfly-borne arboviral fever']",11360,,,C0030372,,,0007437,D010217,066.0,A93.1,,
mondo:0005914,Picornaviridae infectious disease,"['infections, Picornaviridae', 'Picornaviridae infection']",,,,C0031887,,,0007438,D010850,,,,
mondo:0005915,pityriasis versicolor,"['Malassezia furfur infection', 'infection by Pityrosporum furfur', 'tinea versicolor', 'infections, Malassezia furfur']",9060,,,C0040262,,C82981,0007439,D014010,111.0,B36.0,,
mondo:0005916,placenta accreta,"['Percreta, placenta', 'Increta, placenta', 'placenta Percreta', 'placenta Increta', 'accreta, placenta']",4744,,,,,C26856,0007440,D010921,,,,
mondo:0005917,placenta disorder,"['placental disease', 'disease, placental', 'disease, placenta', 'disorders, placenta', 'diseases, placenta', 'placental disorder', 'placenta disorders', 'disorder of placenta', 'placenta disorder', 'disorder, placenta', 'diseases, placental', 'placenta disease', 'placenta diseases', 'placental diseases', 'placenta disease or disorder', 'disease of placenta']",780,,,,,C26857,0007441,D010922,656.70,,,
mondo:0005918,placenta praevia,"['placenta previa', 'placenta praevia']",11060,,,,,C26858,0007442,D010923,,,,
mondo:0005919,placental insufficiency,"['insufficiency, placental', 'uteroplacental vascular insufficiency']",3891,,439167,C0032051,,,0007443,D010927,762.2,,,
mondo:0005920,Plasmodium falciparum malaria,"['malaria fever, subtertian', 'falciparum malaria', 'falciparum malaria [malignant tertian]', 'Plasmodium falciparum malaria, unspecified', 'malignant tertian fever (finding)', 'malignant tertian fever']",14067,,,C0024535,,C34798,0007444,D016778,084.9,,,
mondo:0005921,Plasmodium vivax malaria,"['vivax malaria', 'malaria by Plasmodium vivax']",12978,,,C0024537,,C34800,0007445,D016780,084.1,B51,,
mondo:0005922,pleural tuberculosis,"['tuberculosis of pleura', 'tuberculous pleurisy in primary progressive tuberculosis', 'pearly disease', 'tuberculous pleuritis', 'pleura tuberculosis', 'tuberculous pleurisy']",106,,,,,C26898,0007446,D014396,012.00,A15.6,,
mondo:0005923,Pneumocystis infectious disease,"['infections, Pneumocystis', 'Pneumocystis infection']",,,,C0851886,,,0007447,D016720,,,,
mondo:0005925,pneumonic pasteurellosis,,,,,C0036969,,,0007449,D012766,,,,
mondo:0005927,polyomavirus infectious disease,,,,,C0949804,,,0007451,D027601,,,,
mondo:0005928,post-thrombotic syndrome,"['postphlebetic syndrome with ulcer and inflammation', 'postphlebitic syndrome', 'postphlebetic syndrome with ulcer', 'venous stress disorder', 'postphlebetic syndrome with inflammation']",2364,,,,,,0007452,D011186,459.13,I87.0,,
mondo:0005929,postpartum depression,"['depressive episode with postpartum onset', 'depression, post-partum', 'maternity blues', 'post-Natal depression', 'post-partum depression', 'major depressive episode with peripartum onset', 'post Natal depression', 'depression, postnatal', 'depression, post-Natal', 'postnatal depression', 'postpartum depression', 'post partum depression']",9478,,,,,C92852,0007453,D019052,,F53,,
mondo:0005932,pseudorabies,,,,,C0033839,,,0007457,D011557,,,,
mondo:0005933,pulmonary blastoma,"['lung blastoma', 'blastoma of the lung', 'Pneumoblastoma', 'blastoma of lung', 'pulmonary blastoma']",4765,,64741,C0206629,,C3732,0007458,D018202,162.9,,,
mondo:0005936,recurrent pneumonia,"['recurrent pneumonia', 'recurrent pneumonia (disease)']",,,,,,,0007461,,,,,0006532
mondo:0005937,REM sleep behavior disorder,"['rapid eye movement sleep behaviour disorder', 'rapid eye movement sleep behavior disorder']",9091,,,,,,0007462,D020187,780.59,G47.52,,
mondo:0005938,renal tuberculosis,"['kidney tuberculosis', 'tuberculosis of kidney']",9733,,,C0041328,,C123020,0007463,D014398,016.00,,,
mondo:0005939,Reoviridae infectious disease,"['infections, Reovirus', 'Reovirus infection', 'infections, Reoviridae', 'infection, Reoviridae', 'Reovirus infections', 'infection, Reovirus', 'Reoviridae infection']",,,,C0035112,,,0007464,D012088,,,,
mondo:0005940,respirovirus infectious disease,"['infections, Respirovirus']",,,,C3714630,,,0007465,D010253,,,,
mondo:0005941,retroperitoneal cancer,"['malignant neoplasm of retroperitoneum', 'neoplasm of the retroperitoneum', 'cancer of retroperitoneal space', 'malignant tumor of peritoneum and retroperitoneum', 'malignant retroperitoneal neoplasm', 'tumor of retroperitoneum', 'neoplasm of retroperitoneum', 'retroperitoneal neoplasm', 'malignant retroperitoneal space neoplasm', 'malignant neoplasm of retroperitoneum and peritoneum', 'malignant tumour of peritoneum and retroperitoneum', 'malignant neoplasm of retroperitoneal space', 'malignant retroperitoneal cancer', 'tumour of retroperitoneum']",5875,,,,,C3537,0007466,D012186,158.0,,,
mondo:0005942,Reye syndrome,['Reye^s syndrome'],14525,,3096,C0035400,,C34983,0007467,D012202,331.81,,10039012,
mondo:0005943,Rhabditida infectious disease,"['infection, Rhabditida', 'infections, Rhabditida', 'Rhabditida infection', 'Rhabditida infections']",,,,C0162631,,,0007468,D017196,,,,
mondo:0005944,Rhabdoviridae infectious disease,"['infection, Rhabdoviridae', 'Rhabdoviridae infection', 'infections, Rhabdoviridae']",,,,C0206751,,,0007469,D018353,,,,
mondo:0005945,rhinoscleroma,,11336,,,C0035468,,,0007470,D012226,040.1,,,
mondo:0005946,rhinosporidiosis,"['infection by Rhinosporidium seeberi', 'Rhinosporidium seeberi caused disease or disorder', 'Rhinosporidioses']",2409,,,C0035469,,,0007471,D012227,117.0,B48.1,,
mondo:0005947,rickettsial pneumonia,['Rickettsiaceae caused pneumonia'],,,,C0032307,,,0007472,D011022,484.8,,,
mondo:0005949,roseolovirus infectious disease,['Roseolovirus caused disease or disorder'],,,,C0376549,,,0007474,D019349,,,,
mondo:0005950,Salmonella gastroenteritis,['Salmonella caused gastroenteritis'],,,,,,,0007475,D012478,003.0,,,
mondo:0005952,scarlet fever,['scarlatina'],8596,,,C0036285,,C94575,0007477,D012541,034.1,A38,,
mondo:0005953,scirrhous adenocarcinoma,"['fibrocarcinoma', 'FIBROADENOCARCINOMA, malignant', 'scirrhous carcinoma', 'adenocarcinoma with productive fibrosis', 'scirrhous adenocarcinoma (morphologic abnormality)', 'scirrhous adenocarcinoma']",4024,,,C0007135,,C2928,0007478,D002293,,,,
mondo:0005954,screw worm infectious disease,"['infection, screw worm', 'Cochliomyia hominivorax caused disease or disorder', 'screw worm infections', 'infections, screw worm']",12927,,,,,,0007479,D012610,,,,
mondo:0005956,septicemic plague,,3481,,,C0152936,,,0007481,,020.2,A20.7,,
mondo:0005957,setariasis,"['infectious disease by Setaria', 'Setaria <nematode> caused disease or disorder']",1079,,,C0036850,,,0007482,D012719,,,,
mondo:0005959,sick building syndrome,,2710,,,C0037050,,,0007484,D018877,,,,
mondo:0005960,silicosis,"['silicotuberculosis', 'chronic silicosis', 'accelerated silicosis', 'pneumoconiosis due to silicates', 'silicotic fibrosis of lung', 'silica pneumoconiosis', 'experimental silicosis', 'acute silicosis']",10325,,,C0037116,,C3369,0007485,D012829,502,,,
mondo:0005961,sinusitis,,0050127,,,C0037199,,C35024,0007486,D012852,461.9,,,
mondo:0005962,skeletal tuberculosis,['osteoarticular tuberculosis'],1639,,,C0041324,,,0007487,D014394,015.9,,,
mondo:0005963,sparganosis,"['sparganosis [larval diphyllobothriasis]', 'Spirometra caused disease or disorder', 'infection by sparganum']",10080,,,C0037753,,C35030,0007488,D013031,123.5,B70.1,,
mondo:0005964,sphenoid sinusitis,"['sphenoid bone sinusitis', 'sinusitis of sphenoid bone', 'sphenoidal sinusitis']",10794,,,C0037886,,C35031,0007489,D015524,,,,
mondo:0005965,spinal stenosis,"['lumbar spinal stenosis', 'cervical spinal stenosis', 'spinal stenosis of lumbar region']",6725,,,C0158288,,C177444,0007490,D013130,724.09,,,0003416
mondo:0005966,spleen cancer,"['malignant splenic neoplasm', 'malignant spleen neoplasm', 'cancer of the spleen', 'malignant splenic tumour', 'malignant neoplasm of spleen', 'malignant tumour of spleen', 'spleen neoplasm', 'malignant tumor of the spleen', 'cancer of spleen', 'splenic cancer', 'malignant neoplasm of the spleen', 'malignant tumour of the spleen', 'spleen cancer', 'splenic neoplasm', 'malignant tumor of spleen', 'malignant splenic tumor']",672,,,,,C3539,0007491,D013160,,C26.1,,
mondo:0005967,splenic tuberculosis,,9305,,,C0041331,,,0007492,D014400,017.7,,,
mondo:0005968,sporotrichosis,['rose gardener^s disease'],14484,,826,C0038034,,,0007494,D013174,117.1,B42,10041736,
mondo:0005969,st. Louis encephalitis,"['Saint Louis encephalitis', 'St. Louis encephalitis virus caused infectious encephalitis', 'Neuroinvasive St. Louis encephalitis virus infection']",10845,,83484,C0014060,,,0007495,D004674,062.3,A83.3,10041896,
mondo:0005970,staphylococcal pneumonia,['Staphylococcus caused pneumonia'],,,,,,,0007496,D011023,482.49,,,
mondo:0005971,staphyloenterotoxemia,"['staphylococcal toxemia due to food', 'staphylococcal toxaemia due to food', 'staphyloenterotoxicosis', 'staphylococcal food poisoning']",96,,,C0038159,,C35037,0007497,D013202,005.0,,,
mondo:0005972,streptococcal pneumonia,"['Streptococcus pneumoniae caused pneumonia', 'Streptococcus pneumonia']",0040084,,,C0155862,,,0007499,D011018,482.39,J13,,
mondo:0005973,Strongylida infectious disease,,,,,,,,0007500,D017206,,,,
mondo:0005974,strongyloidiasis,"['infection by Strongyloides', 'Anguilluliasis', 'Anguillulosis', 'disseminated strongyloidiasis']",10955,,76,C0348996,,C128398,0007501,D013322,127.2,,10042254,
mondo:0005975,suppurative otitis media,"['otitis media with effusion - purulent', 'purulent otitis media']",11506,,,C0029888,,,0007503,D010035,382.4,,,
mondo:0005976,syphilis,"['syphilitic chancre', 'Treponema pallidum caused disease or disorder']",4166,,,,,C35055,0007504,D013587,097.9,,10062120,
mondo:0005977,tabes dorsalis,"['tabes dorsalis - neurosyphilis', 'syphilitic myelopathy', 'posterior spinal sclerosis']",10027,,,C0039223,,C35057,0007505,D013606,094.0,A52.11,,
mondo:0005978,theileriasis,"['infection by Theileria', 'theileriosis']",3733,,,C0039753,,,0007506,D013801,136.8,,,
mondo:0005979,thoracic outlet syndrome,"['TOS', 'thoracic outlet compression syndrome', 'TOS - thoracic outlet syndrome']",3103,,97330,C0039984,,C85188,0007507,D013901,,,10048627,
mondo:0005980,tick infestation,['Ixodoidea caused disease or disorder'],4109,,,C0040196,,,0007508,D013984,,,,
mondo:0005981,tick paralysis,,11285,,,C0040197,,,0007509,D013985,,,,
mondo:0005982,tinea infection,"['Tinea', 'ringworm', 'Tinea caused disease or disorder', 'Tinea infection']",12404,,,C0040247,,C112181,0007510,,,,,
mondo:0005983,tinea favosa,['favus'],4336,,,C0040254,,C35072,0007511,D014007,,B35,,
mondo:0005984,tinea pedis,"['pes dermatophytosis', 'dermatophytosis of pes', 'ringworm of foot', 'athlete^s foot', 'dermatophytosis of foot']",12403,,,C0040259,,,0007512,D014008,110.4,B35.3,,
mondo:0005985,Togaviridae infectious disease,['Togaviridae caused disease or disorder'],,,,C0040361,,,0007513,D014036,,,,
mondo:0005986,torovirus infectious disease,['Torovirus caused disease or disorder'],,,,C0206607,,,0007514,D018176,,,,
mondo:0005987,toxascariasis,['Toxascaris caused disease or disorder'],3107,,,C0040522,,,0007515,D017227,,,,
mondo:0005988,toxocariasis,"['visceral larva migrans', 'Toxocara caused disease or disorder', 'Toxocara infection', 'infection by Toxascaris']",9790,,3343,C0040553,,C85194,0007516,D014120,128.0,,10044269,
mondo:0005989,toxoplasmosis,"['disseminated toxoplasmosis', 'Toxoplasma gondii caused disease or disorder']",9965,,,C0040558,,C3418,0007517,D014123,130.9,B58,,
mondo:0005990,tracheitis,"['chronic tracheitis', 'acute tracheitis', 'tracheal mucosa inflammation', 'tracheal Inflammation']",9392,,,C0264322,,C78643,0007518,D014136,464.1,J04.1,,
mondo:0005991,trench fever,"['fevers, trench', 'shin bone fever', 'fever, trench', 'trench fevers', 'trench fever', 'His-Werner disease', 'quintan fever', 'tibialgic fever', 'Bartonella quintana caused disease or disorder', 'bartonellosis due to Bartonella quintana infection', 'Wolhynian fever']",11101,,64694,C0040830,,,0007519,D014205,083.1,A79.0,10044582,
mondo:0005993,Trichomonas vaginitis urogenital infection,"['urogenital Trichomonas', 'Trichomonas vaginitis', 'Trichomonas vaginalis caused disease of genitourinary system', 'Trichomonas vaginalis trichomoniasis']",0050269,,,,,C35083,0007521,D014247,131.09,A59.0,,
mondo:0005994,trichostrongyloidiasis,['Trichostrongyloidea caused disease or disorder'],1255,,,C0040947,,,0007522,D014252,,,,
mondo:0005995,trichostrongylosis,"['Trichostrongyliasis', 'infection by Trichostrongylus', 'Trichostrongylus caused disease or disorder', 'infection by Trichostrongylus species']",1254,,,C0040948,,,0007523,D014253,127.6,B81.2,,
mondo:0005996,trichuriasis,"['Trichuris trichiura infection', 'Trichuris trichiura caused disease or disorder', 'trichocephaliasis', 'trichuriasis infection', 'whipworm disease', 'infection by Trichuris trichura', 'whipworm infection']",1252,,,C0040954,,C128399,0007524,D014257,127.3,B79,,
mondo:0005997,tricuspid valve stenosis,['tricuspid stenosis'],4078,,,C0040963,,C50783,0007525,D014264,,,,0010446
mondo:0005998,trombiculiasis,['Trombiculidae caused disease or disorder'],8399,,,C0041170,,,0007526,D014323,,,,
mondo:0005999,tuberculous empyema,['tuberculous empyema (& pleural)'],14305,,,C0014014,,C34575,0007528,D004654,,,,
mondo:0006000,tuberculous peritonitis,['Mycobacterium tuberculosis caused peritonitis'],9801,,,C0041325,,,0007529,D014395,014.01,A18.31,,
mondo:0006001,urinary schistosomiasis,"['Schistosoma haematobium infection', 'urinary bladder schistosomiasis', 'cystitis with bilharziasis', 'vesical schistosomiasis', 'Schistosoma hematobium infectious disease', 'Schistosoma hematobium infection', 'Schistosoma haematobium', 'bladder schistosomiasis', 'Schistosoma haematobium (& vesical schistosomiasis)', 'schistosomiasis due to Schistosoma haematobium', 'schistosomiasis of bladder']",1394,,,C1704430,,C39294,0007530,D012553,120.0,,,
mondo:0006002,urogenital tuberculosis,"['genitourinary system tuberculosis', 'genitourinary tuberculosis']",2149,,,C0041333,,,0007531,D014401,016.92,,,
mondo:0006003,uterine corpus cancer,"['endometrial cancer', 'uterine corpus cancer', 'uterine (including endometrial) cancer', 'cancer of body of uterus', 'body of uterus cancer', 'cancer of the corpus uteri', 'malignant body of uterus neoplasm', 'malignant neoplasm of body of uterus', 'corpus uteri cancer']",9460,,,,,C61574,0007532,,182,,,
mondo:0006004,vasomotor rhinitis,,4730,,,C0035460,,C34988,0007533,D012223,,J30.0,,
mondo:0006005,Venezuelan equine encephalitis,"['Venezuelan equine encephalitis virus caused disease or disorder', 'Venezuelan equine fever']",9584,,,C0014078,,C35121,0007534,D004685,066.2,A92.2,,
mondo:0006006,verrucous carcinoma,"['warty carcinoma', 'verrucous squamous carcinoma', 'verrucous carcinoma', 'verrucous squamous cell carcinoma', 'verrucous epidermoid carcinoma', 'verrucous epidermoid cell carcinoma', 'verrucous carcinoma NOS (morphologic abnormality)']",3737,,,C0206706,,C3781,0007535,D018289,199.1,,,
mondo:0006007,vesicoureteral reflux,"['vesicoureteral reflux (disease)', 'vesico-ureteral reflux', 'vesicoureteral reflux']",9620,,289365,C0042580,"['0.563', '-0.11176', '-0.402', '0.0854', '-0.0997', '-0.3005', '-0.5444', '0.73', '-0.2788', '-0.0109', '0.581', '-0.6357', '-0.585', '0.8403', '-0.1548', '0.1041', '-0.3354', '-0.2583', '0.5454', '-0.3755', '0.1721', '0.0724', '0.1702', '-0.484', '0.06934', '-0.05548', '-0.0329', '0.2052', '0.2493', '-0.0656', '0.4373', '-0.6963', '0.5107', '0.1304', '-0.4731', '0.0782', '-0.4463', '0.0973', '-0.0822', '-0.1613', '-0.2262', '0.4836', '0.0667', '-0.4187', '-0.2825', '0.1344', '-0.2045', '-0.2164', '-0.005253', '0.728', '-0.471', '-0.03372', '0.451', '-0.541', '-0.506', '0.1508', '-0.7095', '0.10895', '-0.3213', '-0.03192', '0.3062', '0.506', '0.5166', '0.1779', '0.1815', '0.1176', '0.841', '0.4539', '-0.558', '0.3447', '0.10706', '0.894', '0.02863', '-0.3257', '0.06934', '-0.0681', '0.3362', '1.151', '0.1969', '-0.255', '-0.1837', '-0.06207', '-0.08057', '0.1971', '0.6787', '-0.1832', '0.1765', '-0.4375', '0.1273', '-0.1171', '-0.2908', '0.679', '-0.6436', '0.2302', '1.071', '0.1879', '-0.09827', '-0.454', '-0.10223', '0.1736']",,0007536,D014718,593.7,,,0000076
mondo:0006008,vestibular neuronitis,"['epidemic neurolabyrinthitis', 'vestibular neuritis']",12683,,,C0751908,,,0007537,D020338,386.12,H81.2,,
mondo:0006009,viral encephalitis,"['viral encephalitis', 'Viruses caused encephalitis']",646,,98252,C0243010,,C35302,0007538,,,,10058805,
mondo:0006010,salmonid viral hemorrhagic septicemia,,,,,C1135869,,,0007539,D031941,,,,
mondo:0006011,viral hepatitis,"['Hepatitis viral', 'human viral hepatitis', 'viral Hepatitis', 'viral human hepatitis', 'Viruses caused hepatitis', 'unspecified viral hepatitis with hepatic coma', 'viral hepatitis with hepatic coma']",1884,,,C0042721,,C35124,0004196,D006525,573.1,B15-B19,,
mondo:0006012,viral pneumonia,['Viruses caused pneumonia'],10533,,,C0032310,,,0007541,D011024,480.9,,,
mondo:0006013,visna disease,['Visna/maedi virus caused disease or disorder'],,,,C0080323,,,0007542,D016182,,,,
mondo:0006014,vulvovaginal candidiasis,"['candidal: [vulvovaginitis NOS] or [cervix]', 'vulvovaginal candidiasis', 'candidal: cervix', 'candidal vulvovaginitis', 'monilial vulvovaginitis', 'candidiasis of vulva and vagina', 'vaginal candidiasis']",2272,,,C0700345,,C2914,0007543,D002181,112.1,B37.3,,
mondo:0006015,Waterhouse-Friderichsen syndrome,"['Waterhouse–Friderichsen syndrome', 'fatal pneumococcal Waterhouse-Friderichsen syndrome', 'WFS', 'meningococcal hemorrhagic adrenalitis']",9931,,100067,C0043068,,C85225,0007544,D014884,036.3,A39.1,10047847,
mondo:0006018,Wissler syndrome,"['Wissler^s subsepsis allergica', 'Wissler-Fanconi syndrome (finding)', 'Wissler^s syndrome', 'Wissler syndrome']",3047,,,C0043195,,,0007547,D014924,,,,
mondo:0006019,yaws,"['thymosis', 'frambesia tropica', 'frambesia', 'Bouba', 'polypapilloma tropicum', 'endemic treponematoses', 'frambosie', 'Treponema pertenue infection', 'Treponema pallidum subsp. pertenue caused disease or disorder']",10371,,,C0043388,,C41353,0007548,D015001,102.9,A66,,
mondo:0006021,Prinzmetal angina,"['Prinzmetal^s variant angina', 'Prinzmetal^s angina', 'variant angina', 'angina inversa', 'variant angina pectoris']",0111151,,,C2931193,,,1000013,D000788,413.1,,,
mondo:0006022,acidosis disorder,['acidosis'],,,,,,,1000014,,276.2,,,0001941
mondo:0006025,autosomal recessive disease,"['autosomal recessive disease or disorder', 'disease or disorder, autosomal recessive', 'disease, autosomal recessive']",0050737,,,C0265388,,,1000017,,758.5,,,
mondo:0006026,urinary bladder disorder,"['bladder disease', 'disorder of urinary bladder', 'urinary bladder disease or disorder', 'urinary bladder disorder', 'urinary bladder disease', 'bladder disorder', 'disease of urinary bladder']",365,,,C0005686,,C2900,1000018,D001745,596.9,,,
mondo:0006027,breast synovial sarcoma,['breast synovial sarcoma (disease)'],,,,,,,1000019,,,,,
mondo:0006028,cecum adenocarcinoma,"['caecum adenocarcinoma', 'adenocarcinoma of cecum', 'adenocarcinoma of the cecum', 'cecal adenocarcinoma', 'cecum adenocarcinoma']",3039,,,C1332866,,C5543,1000020,,,,,
mondo:0006029,cecum carcinoma,"['carcinoma of cecum', 'carcinoma of caecum', 'carcinoma of the cecum', 'cecum cancer', 'cecum carcinoma', 'caecum carcinoma', 'cecal cancer']",1519,,,C0149640,,C3491,1000021,,,,,
mondo:0006030,chronic cystitis,"['cystitis, chronic']",1680,,,C0221763,,C27008,1000023,,595.2,,,
mondo:0006031,chronic rhinosinusitis,"['sinusitis, chronic']",,,,C0149516,,C35151,1000024,,473.9,,,
mondo:0006032,cystitis,"['urinary bladder inflammation', 'bladder infection']",1679,,,C0010692,,C26738,1000025,D003556,595.9,,,
mondo:0006033,diffuse intrinsic pontine glioma,"['DIPG', 'infiltrative brainstem glioma', 'diffuse midline glioma']",,,497188,C2986658,,C94764,1000026,D000080443,,,,
mondo:0006034,gastric adenosquamous carcinoma,"['stomach adenosquamous carcinoma', 'STAS', 'gastric (stomach) adenosquamous cancer', 'adenosquamous carcinoma of stomach', 'adenosquamous carcinoma of the stomach', 'gastric adenosquamous carcinoma']",5635,,,C1333761,,C5474,1000029,,,,,
mondo:0006035,gastric tubular adenocarcinoma,"['tubular adenocarcinoma of stomach', 'tubular stomach adenocarcinoma', 'stomach tubular adenocarcinoma', 'gastric tubular adenocarcinoma', 'tubular adenocarcinoma of the stomach']",6595,,,C1333791,,C5473,1000030,,,,,
mondo:0006036,granulosa cell tumor,"['tumour of granulosa cell', 'granulosa cell tumor, adult type', 'granulosa cell neoplasm', 'granulosa cell neoplasm (disease)', 'tumor of granulosa cell', 'GRCT', 'neoplasm of granulosa cell', 'granulosa cell tumor, undetermined', 'granulosa cell tumor, adult type (morphologic abnormality)', 'granulosa cell tumor, sarcomatoid', 'granulosa cell tumor']",2999,,,C0018206,,C3070,1000032,D006106,,,,
mondo:0006037,hydrolethalus syndrome,"['Salonen-Herva-Norio syndrome', 'hydrolethalus', 'HLS']",0050779,,2189,C2931104,"['0.11066', '0.09216', '0.128', '-0.1652', '0.4639', '-0.8228', '-0.1866', '0.9927', '-0.3105', '-0.3777', '-0.558', '-0.673', '-0.467', '-0.3525', '-0.47', '-0.04874', '-0.1781', '-0.637', '-0.55', '-0.4307', '0.09406', '-0.128', '0.5845', '-0.6387', '-0.2074', '-0.04572', '-0.1705', '0.663', '0.825', '-0.494', '1.116', '-0.7373', '0.02637', '-0.567', '0.3047', '0.02132', '-0.2573', '-0.0741', '-0.357', '-0.1326', '-0.3657', '0.06744', '0.04114', '-0.4954', '-0.2966', '-0.09406', '0.3604', '0.1643', '-0.2054', '0.1595', '-0.09644', '-0.3994', '-0.4663', '-0.297', '-0.85', '-0.2832', '0.2502', '-0.01371', '-0.02715', '0.1387', '-0.1309', '0.1982', '0.1577', '0.68', '-0.5674', '-0.05692', '0.3464', '-0.11176', '-0.91', '0.534', '-0.469', '0.525', '0.136', '0.9316', '-0.689', '0.408', '0.642', '0.2054', '-0.6797', '-0.3108', '-0.418', '-0.7524', '0.749', '0.698', '0.2448', '-0.395', '0.3943', '0.282', '0.11584', '-0.2249', '-0.03464', '0.1208', '0.1975', '-0.233', '0.629', '0.0863', '0.519', '-0.4448', '0.5225', '-0.04462']",,1000033,C536079,,,,
mondo:0006038,indeterminate colitis,['colitis of indeterminate type'],,,,C0341332,,C27110,1000034,,558.9,K52.3,,
mondo:0006039,infectious colitis,['infectious colitis'],,,,C0277524,,C78359,1000035,,,,,
mondo:0006040,lactic acidosis,,,,,C0001125,,,,D000140,,,,
mondo:0006041,lung carcinoid tumor,"['carcinoid tumour of lung', 'carcinoid tumour (disease) of lung', 'lung carcinoid tumor', 'lung carcinoid tumour (disease)', 'lung carcinoid tumor (disease)', 'pulmonary carcinoid tumour', 'carcinoid tumour of the lung', 'lung carcinoid', 'carcinoid tumor of lung', 'carcinoid tumor of the lung', 'pulmonary carcinoid tumor']",,,,C0280089,,C4038,1000037,,,,,
mondo:0006042,meningeal tuberculosis,"['tubercular meningitis', 'TB meningitis', 'TBM', 'tuberculous meningitis']",,,499004,C0041318,,C84888,1000039,D014390,,,,
mondo:0006043,metaplastic breast carcinoma,"['metaplastic carcinoma of the breast', 'breast metaplastic carcinoma', 'metaplastic breast cancer', 'metaplastic breast carcinoma', 'metaplastic carcinoma of breast']",4680,,213531,C1334708,,C5164,1000040,,,C50.6,,
mondo:0006044,nephrosclerosis,['renal sclerosis'],11664,,,C0027719,,,1000041,D009400,587,,,
mondo:0006045,ovarian clear cell adenocarcinoma,"['clear cell adenocarcinoma of the ovary', 'ovarian clear cell adenocarcinoma', 'clear cell adenocarcinoma of ovary', 'ovary clear cell adenocarcinoma']",5304,,398971,CN205034,,C40078,1000042,,,,,
mondo:0006046,ovarian serous cystadenocarcinoma,['ovarian serous cystadenocarcinoma'],5746,,,C0279663,,C7978,1000043,,,,,
mondo:0006047,pancreatic adenocarcinoma,"['adenocarcinoma of the pancreas', 'pancreas adenocarcinoma', 'PAAD', 'adenocarcinoma - pancreas', 'pancreatic adenocarcinoma', 'adenocarcinoma of pancreas']",4074,,,C0281361,,C8294,1000044,,,,,
mondo:0006049,papillary lung adenocarcinoma,"['lung papillary adenocarcinoma', 'papillary adenocarcinoma of the lung', 'papillary lung adenocarcinoma', 'papillary adenocarcinoma of lung', 'lung papillary-adenocarcinoma']",5588,,,C1335325,,C5650,1000046,,162.9,,,
mondo:0006050,pleomorphic breast carcinoma,['anaplastic breast carcinoma'],,,,C2211689,,C5161,1000047,,,,,
mondo:0006052,pulmonary tuberculosis,"['pulmonary TB', 'lung tuberculosis', 'lung TB']",2957,,,C0041327,,C26899,1000049,D014397,011.96,,,
mondo:0006053,renal leiomyoma,"['leiomyoma of kidney', 'kidney leiomyoma']",,,,,,,1000050,,,,,
mondo:0006054,reproductive system neoplasm,"['neoplasm of the reproductive system', 'tumor of reproductive system', 'reproductive system neoplasm (disease)', 'reproductive tumor', 'tumour of reproductive system', 'reproductive system tumour', 'tumour of the reproductive system', 'reproductive system tumor', 'neoplasm of reproductive system', 'reproductive system neoplasm', 'reproductive neoplasm', 'reproductive tumour', 'tumor of the reproductive system']",,,,C0178830,,C3674,1000051,,,,,
mondo:0006055,sex cord-stromal tumor,"['Sex cord-stromal tumor, no ICD-O subtype (morphologic abnormality)', 'specialised gonadal neoplasm', 'tumour of sex cord', 'Sex cord-stromal neoplasm', 'sex cord-gonadal stromal tumour', 'Sex cord-stromal tumor', 'neoplasm of sex cord', 'specialised gonadal tumour (qualifier value)', 'sex cord tumor', 'Sex cord-stromal tumour', 'specialized gonadal neoplasm', 'specialized gonadal neoplasm (morphologic abnormality)', 'specialized gonadal tumor', 'Sex cord stromal tumour', 'malignant testicular sex cord-stromal tumor', 'Sex cord stromal tumor', 'sex cord tumour', 'specialized gonadal tumor (qualifier value)', 'specialised gonadal neoplasm (morphologic abnormality)', 'malignant testicular sex cord-stromal tumour', 'Sex cord-stromal tumor, no ICD-O subtype', 'sex cord-stromal tumor', 'sex cord-gonadal stromal tumor', 'specialized gonadal neoplasm NOS (morphologic abnormality)', 'tumor of sex cord', 'specialised gonadal neoplasm NOS (morphologic abnormality)', 'specialised gonadal tumour']",192,,,C1515289,,C3794,1000052,,,,,
mondo:0006056,squamous cell breast carcinoma,"['squamous cell breast carcinoma', 'squamous breast carcinoma', 'breast primary squamous cell carcinoma', 'squamous carcinoma of breast', 'primary squamous cell carcinoma of the breast', 'primary squamous cell carcinoma of breast', 'squamous cell carcinoma of breast', 'breast squamous cell carcinoma', 'squamous cell carcinoma of the breast', 'squamous carcinoma of the breast', 'metaplastic squamous cell carcinoma', 'scc of the breast', 'primary squamous cell breast carcinoma', 'scc of breast']",5514,,,C1336079,,C5177,1000053,,,,,
mondo:0006058,Wilms tumor,"['Wilms^ tumour', 'Wilms^ tumor', 'Wilms tumor', 'Wilms tumor (nephroblastoma)', 'Wilms tumour (nephroblastoma)']",,,,CN244940,,C3267,1000056,D009396,,,,
mondo:0006059,nasal cavity squamous cell carcinoma,"['squamous cell carcinoma of the nasal cavity', 'squamous cell carcinoma of nasal cavity', 'nasal cavity squamous cell carcinoma']",5515,,,C0280333,,C8192,1000057,,,,,
mondo:0006060,nasopharyngeal squamous cell carcinoma,,,,,,,C3871,1000058,C538339,,,,
mondo:0006061,cervical artery dissection,,,,,,,,1000059,,,,,
mondo:0006065,lactose intolerance adult type,"['disaccharide intolerance 3', 'adult lactase deficiency', 'hypolactasia, adult type', 'lactase persistence/nonpersistence', 'lactose intolerance, ADULT type']",,223100,319681,,"['0.395', '0.2607', '-0.2874', '0.5254', '0.5293', '0.2021', '-0.7285', '0.0577', '-0.3716', '-0.387', '0.388', '0.2827', '0.006115', '0.6895', '-0.4', '-0.01521', '-0.23', '0.709', '-0.7026', '-0.3228', '-0.4468', '-0.5894', '0.00865', '-0.02258', '0.673', '-0.04614', '-0.1648', '0.1829', '0.51', '-0.289', '0.185', '-0.1929', '-0.1376', '0.4177', '0.2335', '0.917', '-0.3672', '0.6274', '0.2115', '-0.3047', '-0.284', '-0.2783', '-0.05927', '0.09753', '0.2059', '-0.4177', '-0.1714', '-0.3335', '0.523', '0.433', '-0.1399', '-0.4163', '0.1059', '-0.3608', '0.1857', '-0.697', '-0.007256', '0.05185', '-0.3801', '0.3782', '0.4717', '0.557', '0.6143', '-0.1368', '-0.05118', '0.1357', '0.8115', '0.4602', '-0.255', '0.281', '-0.0426', '0.369', '0.153', '-0.1222', '0.36', '0.4995', '0.07', '0.1454', '0.0197', '0.38', '-0.4363', '0.2189', '-0.2913', '-0.05432', '0.03738', '0.3076', '0.4678', '-0.424', '1.183', '-0.4067', '-0.4448', '0.2712', '-0.26', '0.1099', '0.7246', '0.1145', '-0.1512', '-0.66', '-0.597', '0.1486']",,1000063,,,,,
mondo:0006066,"acinar prostate adenocarcinoma, foamy gland variant",,,,,C1515863,,C39882,1000064,,,,,
mondo:0006067,acinar prostate mucinous adenocarcinoma,"['acinar colloid prostate adenocarcinoma', 'colloid adenocarcinoma of the prostate', 'prostate colloid adenocarcinoma', 'colloidal adenocarcinoma of the prostate', 'colloidal adenocarcinoma of prostate', 'mucinous adenocarcinoma of the prostate', 'colloidal prostate adenocarcinoma', 'mucinous adenocarcinoma of prostate', 'colloid adenocarcinoma of prostate']",3703,,,C1335513,,C5537,1000065,,,,,
mondo:0006068,ACTH-producing pituitary gland adenoma,"['corticotroph adenoma', 'ACTH-secreting adenoma of pituitary', 'adrenocorticotropin producing pituitary gland adenoma', 'adrenocorticotropin producing adenoma of the pituitary gland', 'ACTH-secreting adenoma of pituitary gland', 'adrenocorticotropin producing pituitary adenoma', 'ACTH-secreting adenoma of the pituitary gland', 'ACTH-secreting adenoma of the pituitary', 'adrenocorticotropin secreting adenoma of pituitary', 'adrenocorticotropin secreting adenoma of the pituitary', 'ACTH secreting adenoma of pituitary', 'pituitary ACTH secreting adenoma', 'ACTHoma', 'ACTH-producing pituitary adenoma', 'adrenocorticotropin secreting adenoma of pituitary gland', 'adrenocorticotropin secreting pituitary gland adenoma', 'ACTH producing pituitary gland adenoma', 'adrenocorticotropin secreting pituitary adenoma', 'Corticotropinoma', 'adrenocorticotropin producing adenoma of pituitary gland', 'ACTH-producing pituitary gland adenoma', 'corticotropic adenoma', 'corticotropin secreting adenoma of the pituitary', 'pituitary ACTH-secreting adenoma', 'adrenocorticotropin producing adenoma of pituitary', 'pituitary corticotropin secreting adenoma', 'adrenocorticotropin secreting adenoma of the pituitary gland', 'pituitary gland ACTH-secreting adenoma', 'ACTH secreting adenoma of the pituitary', 'adrenocorticotropin producing adenoma of the pituitary', 'corticotropin secreting pituitary gland adenoma']",,,,C1306214,,C7462,1000066,,,,,
mondo:0006069,ACTH-producing pituitary gland carcinoma,"['malignant Corticotropinoma of pituitary', 'malignant ACTH producing tumour of pituitary gland', 'malignant adrenocorticotropin producing neoplasm of the pituitary gland', 'malignant ACTH secreting pituitary tumour', 'malignant adrenocorticotropin producing tumor of the pituitary gland', 'malignant ACTH producing tumor of the pituitary', 'malignant ACTH producing tumor of the pituitary gland', 'malignant adrenocorticotropin producing tumour of pituitary', 'malignant adrenocorticotropin secreting pituitary neoplasm', 'malignant ACTH producing pituitary tumor', 'malignant adrenocorticotropin producing neoplasm of the pituitary', 'malignant ACTH secreting tumour of the pituitary', 'malignant ACTH producing tumor of pituitary gland', 'malignant ACTH secreting pituitary gland tumor', 'malignant adrenocorticotropin producing pituitary gland tumor', 'malignant ACTH producing pituitary gland neoplasm', 'malignant ACTH producing neoplasm of pituitary gland', 'malignant Corticotropinoma of the pituitary', 'malignant adrenocorticotropin producing pituitary neoplasm', 'malignant adrenocorticotropin producing tumor of pituitary', 'malignant adrenocorticotropin producing tumour of the pituitary gland', 'malignant adrenocorticotropin secreting pituitary tumour', 'malignant ACTH secreting tumor of pituitary', 'malignant adrenocorticotropin producing tumour of pituitary gland', 'malignant ACTH secreting neoplasm of pituitary gland', 'malignant adrenocorticotropin producing pituitary gland tumour', 'malignant adrenocorticotropin secreting pituitary tumor', 'malignant adrenocorticotropin producing pituitary gland neoplasm', 'malignant ACTH secreting neoplasm of pituitary', 'malignant ACTH secreting pituitary neoplasm', 'malignant pituitary Corticotropinoma', 'malignant ACTH producing tumour of the pituitary', 'malignant ACTH secreting neoplasm of the pituitary', 'malignant ACTH secreting tumor of the pituitary', 'malignant Corticotropinoma of pituitary gland', 'malignant ACTH producing tumor of pituitary', 'malignant corticotropin secreting pituitary gland neoplasm', 'malignant adrenocorticotropin producing tumor of pituitary gland', 'malignant adrenocorticotropin secreting pituitary gland tumor', 'malignant ACTH secreting tumour of the pituitary gland', 'malignant adrenocorticotropin producing neoplasm of pituitary', 'malignant ACTH producing tumour of pituitary', 'ACTH producing pituitary gland carcinoma', 'malignant ACTH producing pituitary gland tumor', 'malignant ACTH secreting neoplasm of the pituitary gland', 'malignant ACTH secreting tumor of the pituitary gland', 'malignant ACTH secreting tumour of pituitary gland', 'malignant ACTH producing neoplasm of the pituitary', 'malignant ACTH secreting pituitary tumor', 'malignant adrenocorticotropin producing pituitary tumor', 'malignant ACTH secreting tumor of pituitary gland', 'malignant ACTH secreting pituitary gland tumour', 'malignant adrenocorticotropin producing pituitary tumour', 'malignant ACTH producing pituitary tumour', 'malignant adrenocorticotropin producing tumour of the pituitary', 'malignant Corticotropinoma of the pituitary gland', 'malignant adrenocorticotropin secreting pituitary gland neoplasm', 'malignant adrenocorticotropin producing neoplasm of pituitary gland', 'malignant adrenocorticotropin secreting pituitary gland tumour', 'malignant pituitary gland Corticotropinoma', 'malignant ACTH producing pituitary neoplasm', 'malignant ACTH producing neoplasm of pituitary', 'malignant ACTH producing neoplasm of the pituitary gland', 'malignant ACTH secreting tumour of pituitary', 'malignant ACTH producing pituitary gland tumour', 'malignant adrenocorticotropin producing tumor of the pituitary', 'malignant ACTH producing tumour of the pituitary gland']",6276,,,C1334556,,C5964,1000067,,,,,
mondo:0006071,adenofibroma,"['female reproductive system adenofibroma', 'benign mixed Muellerian tumour', 'adenofibroma, no ICD-O subtype', 'adenofibroma, benign', 'adenofibroma, no ICD-O subtype (morphologic abnormality)', 'benign mixed Muellerian tumor']",2683,,,C0001422,,C8984,1000070,D000232,,,,
mondo:0006073,adenomatoid odontogenic tumor,['adenomatoid odontogenic neoplasm'],,,,,,C4310,1000072,C538229,,,,
mondo:0006074,adenosquamous carcinoma,"['mixed adenocarcinoma and epidermoid carcinoma', 'adenosquamous cell carcinoma', 'adenosquamous carcinoma', 'mixed adenocarcinoma and squamous carcinoma', 'mixed adenocarcinoma and epidermoid cell carcinoma', 'carcinoma, adenosquamous, malignant', 'mixed adenocarcinoma and squamous cell carcinoma', 'adenosquamous carcinoma (morphologic abnormality)']",4830,,,C0206623,,C3727,1000073,D018196,,,,
mondo:0006075,adrenal gland myelolipoma,"['Myelolipoma', 'MYELOLIPOMA, benign', 'adrenal gland myelolipoma']",,,,C0206635,,C3736,1000074,D018209,,,,
mondo:0006076,adrenal gland neuroblastoma,"['neuroblastoma of the adrenal', 'neuroblastoma of adrenal', 'neuroblastoma of the adrenal gland', 'adrenal neuroblastoma', 'adrenal gland neuroblastoma', 'neuroblastoma of adrenal gland']",5718,,,C0559460,,C4827,1000075,,,,,
mondo:0006077,adrenal medullary hyperplasia,['adrenal medulla hyperplasia'],,,,,,C35838,1000076,,,,,
mondo:0006078,AIDS-related primary central nervous system lymphoma,"['AIDS-related lymphoma of primary central nervous system', 'AIDS-related primary CNS lymphoma', 'AIDS related primary CNS lymphoma', 'AIDS related primary central nervous system lymphoma', 'AIDS-related lymphoma of the primary central nervous system', 'AIDS related lymphoma of primary central nervous system', 'AIDS related lymphoma of the primary central nervous system']",,,,C0281241,,C8284,1000077,,,,,
mondo:0006079,ameloblastic carcinoma,"['odontoma, ameloblastic, malignant', 'ameloblastic carcinoma']",,,314422,C1314678,,C7492,1000078,,,,,
mondo:0006081,anal melanoma,"['malignant melanoma of the anus', 'anus melanoma (disease)', 'anal malignant melanoma', 'melanoma of the anus', 'malignant anus melanoma', 'anal melanoma', 'melanoma of anus', 'malignant melanoma of anus']",14145,,,C0349538,,C4639,1000080,,,,,
mondo:0006082,anal squamous cell carcinoma,"['epidermoid anal carcinoma', 'squamous cell carcinoma of the anus', 'anal squamous cell cancer', 'epidermoid carcinoma of the anus', 'anal squamous cell carcinoma', 'squamous cell carcinoma of anus', 'ANSC', 'anus squamous cell carcinoma', 'epidermoid carcinoma of anus', 'squamous cell anal carcinoma', 'squamous cell carcinoma - anus']",5525,,,C1412036,,C9161,1000081,,,,,
mondo:0006085,angiolipoma,"['angiolipoma, benign']",3616,,,C0206632,,C3733,1000085,D018206,,,,
mondo:0006086,angiomyxoma,,,,,C0027149,,C3254,1000087,,215.9,,,
mondo:0006087,appendix adenocarcinoma,"['adenocarcinoma of appendix', 'appendiceal adenocarcinoma', 'APAD', 'adenocarcinoma of the appendix', 'vermiform appendix adenocarcinoma', 'appendix adenocarcinoma']",3608,,,C0238003,,C7718,1000088,,,,,
mondo:0006088,appendix adenoma,"['appendix adenoma', 'vermiform appendix adenoma']",,,,C1706829,,C43550,1000089,,,,,
mondo:0006090,appendix hyperplastic polyp,"['appendix metaplastic polyp', 'vermiform appendix hyperplastic polyp']",,,,C3272761,,C96416,1000091,,,,,
mondo:0006091,appendix neuroendocrine tumor G1,"['appendix carcinoid endocrine tumour', 'vermiform appendix NET G1', 'vermiform appendix carcinoid tumour (disease)', 'vermiform appendix neuroendocrine tumor, well differentiated, low grade', 'vermiform appendix carcinoid tumor (disease)', 'vermiform appendix carcinoid tumour', 'appendix neuroendocrine tumour G1 (carcinoid)', 'appendix carcinoid tumour', 'carcinoid tumor of appendix', 'carcinoid tumour of the appendix', 'grade 1 neuroendocrine neoplasm of vermiform appendix', 'appendix NET G1', 'carcinoid tumour of appendix', 'appendix carcinoid endocrine tumor', 'appendiceal carcinoid tumor', 'vermiform appendix carcinoid tumor', 'appendix neuroendocrine tumor G1 (carcinoid)', 'carcinoid tumor of the appendix', 'appendiceal carcinoid tumour', 'appendix NET G1 (carcinoid)', 'appendix carcinoid tumor']",0050911,,,C0334298,,C4138,1000092,,209.11,,,
mondo:0006092,appendix villous adenoma,"['vermiform appendix villous adenoma', 'appendix villous adenoma', 'villous adenoma of the appendix', 'villous adenoma of appendix']",,,,C1332329,,C5512,1000093,,,,,
mondo:0006093,ascending colon neuroendocrine tumor G1,"['ascending colon carcinoid tumor', 'ascending colon neuroendocrine tumor G1', 'carcinoid tumour of ascending colon', 'ascending colon NET G1', 'carcinoid tumour of the ascending colon', 'carcinoid tumor of ascending colon', 'ascending colon carcinoid tumour', 'ascending colon carcinoid tumour (disease)', 'ascending colon neuroendocrine tumor, well differentiated, low grade', 'carcinoid tumor of the ascending colon', 'grade 1 neuroendocrine neoplasm of ascending colon', 'ascending colon carcinoid tumor (disease)']",,,,C1332340,,C6427,1000094,,,,,
mondo:0006094,Askin tumor,"['PNET of thoracopulmonary region', 'peripheral neuroectodermal tumour of thoracopulmonary region', 'Askin^s tumor', 'Askin tumor', 'peripheral neuroectodermal tumor of thoracopulmonary region', 'small cell tumour of thoracopulmonary region', 'Askin^s tumour', 'small cell tumor of thoracopulmonary region']",0050608,,,C0877849,,C7542,1000095,C563168,,,,
mondo:0006095,atypical carcinoid tumor,"['atypical carcinoid tumor', 'malignant carcinoid tumour', 'malignant carcinoid tumor']",,,,C1266032,,C72074,1000097,,,,,
mondo:0006096,atypical endometrial hyperplasia,"['endometrial hyperplasia with atypia', 'atypical hyperplasia of endometrium', 'atypical hyperplasia of the endometrium']",,,,C0349579,,C4654,1000098,,621.33,,,
mondo:0006097,atypical lipomatous tumor,"['well differentiated liposarcoma', 'lipoma-like liposarcoma', 'ALT', 'liposarcoma, well differentiated (morphologic abnormality)', 'Atypical lipoma', 'well differentiated liposarcoma of superficial soft tissue', 'superficial well differentiated liposarcoma']",5690,,,C1370889,,C6505,1000099,,,,,
mondo:0006098,atypical lobular breast hyperplasia,"['atypical lobular breast hyperplasia', 'atypical lobular hyperplasia of the breast', 'atypical lobular hyperplasia of breast', 'atypical lobular hyperplasia', 'ALH', 'atypical breast lobular hyperplasia']",,,,,,C4730,1000100,,610.8,,,
mondo:0006102,basaloid carcinoma,['basaloid carcinoma'],,,,,,C4121,1000105,,,,,
mondo:0006103,benign adrenal gland pheochromocytoma,"['benign adrenal gland pheochromocytoma', 'pheochromocytoma, benign', 'adrenal gland pheochromocytoma, benign']",,,,,,C48305,1000106,,,,,
mondo:0006104,benign carotid body paraganglioma,"['chemodectoma, benign', 'benign carotid body paraganglioma', 'benign chemodectoma', 'carotid body paraganglioma, benign']",,,,C2698359,,C79950,1000108,,,,,
mondo:0006105,benign conjunctival neoplasm,"['benign conjunctival tumour', 'benign tumor of conjunctiva', 'benign tumour of conjunctiva', 'benign conjunctival neoplasm', 'benign conjunctiva tumour', 'benign conjunctiva neoplasm', 'benign neoplasm of conjunctiva', 'benign conjunctiva tumor', 'conjunctiva benign neoplasm', 'benign neoplasm of the conjunctiva', 'benign conjunctival tumor', 'benign tumour of the conjunctiva', 'benign tumor of the conjunctiva']",,,,C0154025,,C3622,1000110,,,,,
mondo:0006106,benign smooth muscle neoplasm,"['benign tumour of smooth muscle', 'benign neoplasm of smooth muscle', 'benign smooth muscle tumor', 'benign neoplasm of the smooth muscle', 'benign smooth muscle neoplasm', 'benign tumor of smooth muscle', 'smooth muscle tissue benign neoplasm', 'benign smooth muscle tumour', 'benign tumour of the smooth muscle', 'benign tumor of the smooth muscle']",,,,C1332539,,C6510,1000121,,,,,
mondo:0006107,benign thyroid gland neoplasm,"['benign thyroid tumor', 'benign thyroid neoplasm', 'benign tumour of the thyroid', 'benign tumour of the thyroid gland', 'thyroid neoplasm, benign', 'benign thyroid gland tumor', 'benign tumor of the thyroid gland', 'thyroid gland benign neoplasm', 'benign neoplasm of thyroid', 'benign neoplasm of the thyroid', 'benign tumor of thyroid', 'benign neoplasm of thyroid gland', 'benign tumor of the thyroid', 'benign tumour of thyroid gland', 'benign thyroid gland neoplasm', 'benign tumour of thyroid', 'benign thyroid tumour', 'benign tumor of thyroid gland', 'benign thyroid gland tumour', 'benign neoplasm of the thyroid gland', 'benign neoplasm of thyroid glands']",,,,C0154038,,C3628,1000122,,226,,,
mondo:0006108,bile duct adenoma,"['bile duct adenoma (morphologic abnormality)', 'CHOLANGIOMA, benign', 'Cholangioma', 'adenoma of bile duct', 'Cholangioadenoma', 'Hepatocholangioma', 'Hepatocholangiocellular adenoma', 'bile duct adenoma', 'adenoma of the bile duct']",5381,,,C0008309,,C2942,1000123,D002759,,,,
mondo:0006109,malignant biphasic mesothelioma,"['biphasic mesothelioma', 'mesothelioma, biphasic, malignant (morphologic abnormality)', 'malignant biphasic mesothelioma, malignant', 'mesothelioma, biphasic, malignant', 'malignant biphasic mesothelioma', 'malignant mixed mesothelioma', 'mixed mesothelioma']",4486,,,C0334515,,C4282,1000124,,,,,
mondo:0006111,bladder flat intraepithelial lesion,"['flat intraepithelial lesion of the urinary bladder', 'bladder flat intraepithelial lesion', 'urinary bladder flat intraepithelial lesion', 'flat intraepithelial lesion of the bladder']",5429,,,C1332559,,C37266,1000126,,,,,
mondo:0006112,bladder inflammatory myofibroblastic tumor,"['bladder inflammatory myofibroblastic tumor', 'inflammatory myofibroblastic neoplasm of the bladder', 'inflammatory myofibroblastic tumour of the urinary bladder', 'inflammatory myofibroblastic tumour of urinary bladder', 'inflammatory myofibroblastic tumour of the bladder', 'urinary bladder inflammatory myofibroblastic tumor', 'inflammatory myofibroblastic tumor of urinary bladder', 'inflammatory myofibroblastic tumor of the bladder', 'inflammatory myofibroblastic tumour of bladder', 'inflammatory myofibroblastic bladder tumor', 'inflammatory myofibroblastic neoplasm of bladder', 'urinary bladder inflammatory myofibroblastic tumour', 'inflammatory myofibroblastic bladder tumour', 'inflammatory myofibroblastic neoplasm of the urinary bladder', 'inflammatory myofibroblastic tumor of bladder', 'inflammatory myofibroblastic neoplasm of urinary bladder', 'bladder inflammatory myofibroblastic neoplasm', 'urinary bladder inflammatory myofibroblastic neoplasm', 'inflammatory myofibroblastic tumor of the urinary bladder']",,,,C1336891,,C6177,1000127,,,,,
mondo:0006115,"blast phase chronic myelogenous leukemia, BCR-ABL1 positive","['blastic phase chronic myeloid leukemia', 'crises, blast', 'blast phase', 'blast phase chronic granulocytic leukemia', 'crisis, blast', 'blast crisis', 'blast phases', 'blast phase chronic myeloid leukaemia', 'blast phase chronic granulocytic leukaemia', 'blastic phase chronic myelocytic leukemia', 'blast phase chronic myelogenous leukaemia', 'blastic phase chronic myelogenous leukemia', 'blast phase chronic myeloid leukemia', 'blast phase chronic myelocytic leukemia', 'blastic phase chronic myeloid leukaemia', 'phases, blast', 'blastic phase chronic myelogenous leukaemia', 'blastic phase chronic granulocytic leukaemia', 'blast phase chronic myelogenous leukemia', 'blastic phase chronic granulocytic leukemia', 'blastic phase CML', 'blast phase CML', 'blast phase chronic myelocytic leukaemia', 'blast crises', 'phase, blast', 'blastic phase chronic myelocytic leukaemia']",,,,C0005699,,C9110,1000131,D001752,,,,
mondo:0006116,breast carcinoma by gene expression profile,['breast carcinoma by gene expression profile'],,,,C3642344,,C53553,1000143,,,,,
mondo:0006117,breast diffuse large B-cell lymphoma,"['breast DLBCL', 'diffuse large B-cell lymphoma of breast', 'breast diffuse large B-cell lymphoma']",,,,C1511306,,C40375,1000144,,,,,
mondo:0006118,breast fibrosis,"['fibrosis of breast', 'breast fibrosclerosis', 'fibrosclerosis of breast', 'breast fibrosis', 'fibrosis of the breast', 'fibrosclerosis of the breast']",10353,,,C0156318,,C3660,1000145,,610.3,N60.3,,
mondo:0006119,breast mucosa-associated lymphoid tissue lymphoma,"['breast mucosa-associated lymphoid tissue lymphoma', 'breast MALT lymphoma']",,,,C1332633,,C35688,1000146,,,,,
mondo:0006120,C-cell hyperplasia,['C-cell hyperplasia'],,,,C0342190,,C46100,1000147,,,,,
mondo:0006121,calcifying fibrous tumor,"['CFT', 'calcifying fibrous tumor', 'calcifying fibrous pseudotumor']",,,,C1332833,,C6488,1000148,,,,,
mondo:0006122,calcifying nested epithelial stromal tumor of the liver,,,,,C3273067,,C96830,1000149,,,,,
mondo:0006123,cardiac rhabdomyoma,"['rhabdomyoma of heart', 'cardiac rhabdomyoma (disease)', 'cardiac rhabdomyoma', 'rhabdomyoma of the heart', 'heart rhabdomyoma']",,,,C1332852,,C6739,1000150,,,,,0009729
mondo:0006126,cecum neuroendocrine tumor G1,"['caecum carcinoid tumour (disease)', 'caecal carcinoid tumor', 'carcinoid tumor of cecum', 'cecal carcinoid tumor', 'caecum carcinoid tumor (disease)', 'carcinoid tumour of cecum', 'caecum carcinoid tumor', 'cecal carcinoid tumour', 'cecum carcinoid tumor', 'caecum carcinoid tumour', 'carcinoid tumor of the cecum', 'carcinoid tumour of the cecum', 'cecum carcinoid tumour', 'cecum NET G1', 'caecum NET G1', 'cecum neuroendocrine tumor G1', 'caecal carcinoid tumour', 'grade 1 neuroendocrine neoplasm of caecum', 'caecum neuroendocrine tumor, well differentiated, low grade']",,,,C0854488,,C5501,1000154,,,,,
mondo:0006128,central nervous system anaplastic large cell lymphoma,"['anaplastic central nervous system large cell lymphoma', 'anaplastic large cell lymphoma of the CNS', 'central nervous system anaplastic large cell lymphoma', 'anaplastic large cell lymphoma of central nervous system', 'anaplastic CNS large cell lymphoma', 'anaplastic large cell lymphoma of the central nervous system', 'primary central nervous system anaplastic large cell lymphoma', 'anaplastic large cell lymphoma of CNS', 'primary CNS anaplastic large cell lymphoma']",,,,C1335476,,C5322,1000156,,,,,
mondo:0006130,central nervous system neoplasm,"['CNS neoplasm', 'CNS tumor', 'tumour of the CNS', 'central nervous system neoplasm (disease)', 'tumor of CNS', 'neoplasm of the central nervous system', 'brain/spinal cord tumour', 'neoplasm of central nervous system', 'tumor of central nervous system', 'tumour of central nervous system', 'brain/spinal cord tumor', 'tumor of the CNS', 'tumor of the central nervous system', 'central nervous system tumor', 'central nervous system neoplasm', 'CNS tumour', 'neoplasm of CNS', 'tumour of CNS', 'tumour of the central nervous system', 'central nervous system tumour']",,,,,,C9293,1000158,,,,,
mondo:0006131,cerebellar liponeurocytoma,"['cerebellar liponeurocytoma', 'cerebellar liponeurocytoma (WHO grade II)', 'CLNC', 'lipomatous medulloblastoma (formerly)', 'lipomatous medulloblastoma']",6458,,251931,C1370507,,C6905,1000159,,,,,
mondo:0006132,cervical adenoid basal carcinoma,['cervical adenoid basal cancer'],6428,,,C1516403,,C40213,1000160,,,,,
mondo:0006133,cervical adenoid cystic carcinoma,"['adenoid cystic carcinoma of the cervix uteri', 'adenoid cystic carcinoma of cervix', 'cervical adenoid cystic carcinoma', 'cervical adenoid cystic cancer', 'cervix uteri adenoid cystic carcinoma', 'uterine cervix adenoid cystic carcinoma', 'adenoid cystic carcinoma of the uterine cervix', 'adenoid cystic carcinoma of cervix uteri', 'adenoid cystic carcinoma of uterine cervix', 'adenoid cystic carcinoma of the cervix']",4867,,213823,C1332911,,C6346,1000161,,,C53.0,,
mondo:0006134,cervical adenosquamous carcinoma,"['cervical adenosquamous cell carcinoma', 'adenosquamous cell carcinoma of the cervix uteri', 'cervical adenosquamous carcinoma', 'adenosquamous cell carcinoma of the cervix', 'cervix uteri adenosquamous cell carcinoma', 'adenosquamous cell carcinoma of cervix', 'cervix adenosquamous cell carcinoma', 'adenosquamous cell carcinoma of the uterine cervix', 'adenosquamous cell carcinoma of cervix uteri', 'adenosquamous cell carcinoma of uterine cervix', 'cervical adenosquamous cancer', 'uterine cervix adenosquamous cell carcinoma', 'adenosquamous carcinoma of cervix']",5636,,,C0346202,,C4519,1000162,,,,,
mondo:0006135,cervical clear cell adenocarcinoma,"['uterine cervix clear cell carcinoma', 'uterine cervix clear cell adenocarcinoma', 'clear cell adenocarcinoma of cervix uteri', 'cervix uteri clear cell adenocarcinoma', 'clear cell adenocarcinoma of cervix', 'clear cell adenocarcinoma of the uterine cervix', 'clear cell carcinoma of cervix', 'clear cell adenocarcinoma of the cervix', 'clear cell carcinoma of cervix uteri', 'clear cell carcinoma of the cervix', 'clear cell carcinoma of the cervix uteri', 'clear cell carcinoma of the uterine cervix', 'clear cell carcinoma of uterine cervix', 'clear cell adenocarcinoma of uterine cervix', 'cervical clear cell adenocarcinoma', 'clear cell adenocarcinoma of the cervix uteri', 'cervix clear cell carcinoma', 'cervix uteri clear cell carcinoma', 'cervix clear cell adenocarcinoma', 'cervical clear cell carcinoma']",5303,,,C1332912,,C6344,1000163,,,,,
mondo:0006137,cervical intraepithelial neoplasia grade 2/3,['CIN 2/3'],,,,C2986622,,C94676,1000166,,,,,
mondo:0006138,cervical large cell neuroendocrine carcinoma,"['cervical large cell neuroendocrine carcinoma', 'cervical neuroendocrine tumor', 'cervical neuroendocrine tumour']",6659,,,C1516417,,C40214,1000167,,,,,
mondo:0006139,cervical metaplasia,,,,,C0281796,,,1000168,,,,,
mondo:0006140,"cervical mucinous adenocarcinoma, minimal deviation variant","['cervical adenoma malignum', 'cervical mucinous adenocarcinoma, minimal deviation variant', 'cervical mucinous adenocarcinoma, minimal deviation type']",6627,,,C1516423,,C40206,1000169,,,,,
mondo:0006141,cervical villoglandular adenocarcinoma,"['cervical adenocarcinoma, villoglandular variant', 'cervical villoglandular adenocarcinoma', 'cervical villoglandular carcinoma', 'villoglandular variant cervical mucinous adenocarcinoma', 'villoglandular adenocarcinoma of the cervix']",8338,,,C4289808,,C40208,1000170,,,,,
mondo:0006142,cervical small cell carcinoma,"['small cell carcinoma of uterine cervix', 'cervix uteri small cell carcinoma', 'cervical small cell carcinoma', 'small cell carcinoma of the uterine cervix', 'SCCE', 'small cell carcinoma of cervix', 'cervix small cell carcinoma', 'small cell carcinoma of cervix uteri', 'uterine cervix small cell carcinoma', 'small cell carcinoma of the cervix uteri', 'small cell carcinoma of the cervix', 'Cervical small cell cancer']",6740,,,C0279674,,C7982,1000171,,,,,
mondo:0006143,cervical squamous cell carcinoma,"['squamous cervical cancer', 'squamous cell carcinoma of cervix uteri', 'squamous cell carcinoma of the cervix', 'CESC', 'uterine cervix squamous cell carcinoma', 'cervical squamous cell cancer', 'squamous cell carcinoma of the cervix uteri', 'squamous cell carcinoma of uterine cervix', 'cervical squamous cell carcinoma', 'cervix squamous cell carcinoma', 'cervix uteri squamous cell carcinoma', 'squamous cell carcinoma of the uterine cervix', 'squamous cell carcinoma of cervix']",3744,,213767,C0279671,,C4028,1000172,,,C53.0,,
mondo:0006144,cervical Wilms tumor,"['cervical Wilms^ tumor', 'cervical Wilms^ tumour', 'cervical Wilms tumor']",5190,,,C1516437,,C40236,1000173,,,,,
mondo:0006145,chondroid chordoma,"['chondroid chordoma', 'chondroid chordoma (morphologic abnormality)']",4152,,,C1266173,,C6902,1000174,,,,,
mondo:0006146,chondroid hamartoma,,,,,C1707390,,C42589,1000175,,,,,
mondo:0006149,clear cell papillary cystadenoma,['clear cell papillary cystadenoma'],,,,C1880102,,C65203,1000181,,,,,
mondo:0006150,colon Burkitt lymphoma,"['Burkitts lymphoma of colon', 'primary colon Burkitt^s lymphoma', 'colon Burkitts lymphoma', 'colon Burkitt lymphoma', 'colon Burkitt^s lymphoma']",,,,C1333083,,C27465,1000182,,,,,
mondo:0006151,colon dysplasia,"['colonic dysplasia', 'dysplasia of colon', 'dysplasia of the colon']",,,,C1302363,,C4847,1000183,,,,,
mondo:0006152,colon inflammatory polyp,"['inflammatory polyp of colon', 'colonic inflammatory polyp', 'inflammatory polyp of the colon']",,,,C0267392,,C5517,1000184,,,,,
mondo:0006153,colon juvenile polyp,"['juvenile polyp of the colon', 'colonic retention polyp', 'colonic juvenile polyp', 'juvenile polyp of colon', 'retention polyp of the colon', 'retention polyp of colon', 'colon retention polyp']",,,,C1333090,,C5518,1000185,,,,,
mondo:0006154,colon mucosa-associated lymphoid tissue lymphoma,"['MALToma of the colon', 'MALT lymphoma of the colon', 'MALToma of colon', 'MALT lymphoma of colon', 'colonic mucosa-associated lymphoid tissue lymphoma', 'colonic MALToma', 'colon MALT lymphoma', 'colon MALToma', 'colonic MALT lymphoma']",,,,C1333096,,C5498,1000186,,,,,
mondo:0006155,colon neuroendocrine tumor G1,"['carcinoid tumour of the colon', 'colon carcinoid tumour', 'colon carcinoid tumour (disease)', 'grade 1 neuroendocrine neoplasm of colon', 'colonic carcinoid tumor', 'colon carcinoid tumor (disease)', 'colon NET G1', 'carcinoid tumor of the colon', 'colon neuroendocrine tumor G1', 'colon carcinoid tumor', 'colon neuroendocrine tumor, well differentiated, low grade', 'carcinoid tumour of colon', 'colonic carcinoid tumour', 'carcinoid tumor of colon']",,,,,,C5497,1000188,,,,,
mondo:0006156,colon sessile serrated adenoma/polyp,"['colon sessile serrated adenoma/polyp', 'colon SSP', 'colon sessile serrated polyp', 'colon SSA', 'colon sessile serrated adenoma', 'colon SSA/P']",,,,C3272791,,C96464,1000189,,,,,
mondo:0006157,colorectal adenosquamous carcinoma,"['colorectal adenosquamous carcinoma', 'colorectal (colon or rectal) adenosquamous cancer', 'colorectum adenosquamous carcinoma', 'colorectal adenosquamous cancer']",,,,C1707437,,C43589,1000190,,,,,
mondo:0006158,colorectal diffuse large B-cell lymphoma,"['colorectal DLBCL', 'diffuse large B-cell lymphoma of colorectum', 'colorectum diffuse large B-cell lymphoma', 'colorectal diffuse large B-cell lymphoma']",,,,C3272827,,C96503,1000191,,,,,
mondo:0006159,colorectal gastrointestinal stromal tumor,"['colorectal (colon or rectal) gastrointestinal stromal tumour (gist)', 'colorectal (colon or rectal) gastrointestinal stromal tumor (gist)', 'colorectal gastrointestinal stromal tumour (gist)', 'colorectal gastrointestinal stromal tumor', 'colorectal gastrointestinal stromal tumor (gist)', 'colorectal gist']",,,,C1333109,,C27735,1000192,,,,,
mondo:0006160,colorectal hamartoma,"['colorectal hamartoma', 'large intestinal hamartoma', 'colorectum hamartoma (disease)']",,,,C3272801,,C96474,1000193,,,,,
mondo:0006161,colorectal juvenile polyp,"['colorectal retention polyp', 'juvenile polyp of large bowel', 'large bowel juvenile polyp', 'juvenile polyp of the large bowel', 'large intestinal juvenile polyp']",,,,,,C5681,1000194,,,,,
mondo:0006162,colorectal neuroendocrine tumor G1,"['colorectum NET G1', 'colorectal carcinoid tumour', 'colorectal neuroendocrine tumor G1', 'colorectal carcinoid tumor', 'colorectal NET G1', 'colorectum carcinoid tumor', 'colorectum neuroendocrine tumor, well differentiated, low grade', 'colorectum carcinoid tumour', 'large intestinal neuroendocrine tumor G1', 'grade 1 neuroendocrine neoplasm of colorectum', 'large intestinal neuroendocrine tumour G1']",,,,C3272611,,C96160,1000195,,,,,
mondo:0006163,colorectal serrated adenocarcinoma,['colorectal serrated adenocarcinoma'],,,,C3272809,,C96485,1000196,,,,,
mondo:0006164,colorectal sessile serrated adenoma/polyp,"['colorectal sessile serrated polyp', 'colorectal SSA', 'colorectal mixed hyperplastic adenomatous polyp', 'colorectal mixed hyperplastic adenomatous polyp/serrated adenoma', 'colorectal sessile serrated adenoma', 'colorectal sessile serrated adenoma/polyp', 'colorectal SSP', 'colorectal SSA/P']",,,,C2826783,,C83176,1000197,,,,,
mondo:0006165,colorectal squamous cell carcinoma,"['colorectal squamous cell cancer', 'colorectum squamous cell carcinoma', 'colorectal squamous cell carcinoma', 'colorectal (colon or rectal) squamous cell cancer']",,,,C1707442,,C43588,1000198,,,,,
mondo:0006166,columnar cell hyperplasia of the breast,"['CCH', 'columnar cell hyperplasia of breast']",,,,C1707446,,C54183,1000199,,,,,
mondo:0006167,combined lung carcinoma,"['combined lung carcinoma', 'combined carcinoma of the lung', 'combined lung cancer', 'combined carcinoma of lung']",,,,C1333123,,C7591,1000200,,,,,
mondo:0006169,complex endometrial hyperplasia,,,,,C0349578,,C35423,1000202,,621.32,,,
mondo:0006170,conjunctival disorder,"['disorder of conjunctiva', 'conjunctiva disease', 'conjunctival disease', 'conjunctival disorder', 'disease of conjunctiva', 'conjunctiva disease or disorder']",4251,,,,,C27605,1000203,,,H10-H11,,
mondo:0006172,conjunctival nevus,"['Nevus of conjunctiva', 'Nevus of the conjunctiva', 'conjunctival nevus']",0050906,,,C0346363,,C4551,1000205,,,,,
mondo:0006173,conjunctival squamous cell carcinoma,"['conjunctival squamous cell carcinoma', 'conjunctival squamous cell cancer', 'conjunctival epidermoid carcinoma', 'conjunctiva epidermoid carcinoma', 'ocular surface squamous neoplasia', 'conjunctiva squamous cell carcinoma', 'squamous cell carcinoma of the conjunctiva', 'epidermoid carcinoma of conjunctiva', 'epidermoid carcinoma of the conjunctiva', 'squamous cell carcinoma of conjunctiva', 'invasive squamous cell carcinoma of the conjunctiva']",1748,,,C0346359,,C4549,1000206,,,,,
mondo:0006174,cortisol-producing adrenal cortex adenoma,"['cortisol-producing adrenal cortex adenoma', 'cortisol producing adrenal cortical adenoma', 'cortisol producing adrenal cortex adenoma']",,,,C1707525,,C48449,1000208,,,,,
mondo:0006176,cribriform carcinoma,['cribriform carcinoma'],,,,C0205643,,C3680,1000210,,,,,
mondo:0006178,dedifferentiated solitary fibrous tumor,,,,,C2699572,,C79948,1000214,,,,,
mondo:0006179,desmoplastic ameloblastoma,['desmoplastic ameloblastoma'],,,,C0457533,,C39758,1000215,,,,,
mondo:0006180,digestive system adenoma,"['digestive system adenoma', 'digestive tract adenoma', 'gastrointestinal adenoma', 'GI adenoma']",4147,,,C0948101,,C36207,1000217,,,,,
mondo:0006181,digestive system carcinoma,"['carcinoma of digestive system', 'carcinoma of the gastrointestinal system', 'digestive system carcinoma', 'gastrointestinal carcinoma', 'gastrointestinal carcinoma (disease)', 'gastrointestinal system carcinoma']",0050922,,,C0151544,,C96963,1000218,,,,,0002672
mondo:0006182,digestive system mixed adenoneuroendocrine carcinoma,"['gastrointestinal mixed Adenoneuroendocrine carcinoma', 'digestive system Mixed Adenoneuroendocrine cancer', 'digestive system mixed adenoneuroendocrine carcinoma', 'gastrointestinal MANEC', 'mixed Adenoneuroendocrine carcinoma', 'MANEC']",,,,C2987129,,C95406,1000219,,,,,
mondo:0006183,disseminated peritoneal leiomyomatosis,"['disseminated peritoneal leiomyomatosis', 'DPL', 'diffuse peritoneal leiomyomatosis', 'LPD', 'leiomyomatosis peritonealis disseminate', 'leiomyomatosis peritonealis disseminata']",5728,,71274,C0267785,,C3958,1000220,,,,,
mondo:0006184,ductal breast carcinoma in situ and lobular carcinoma in situ,"['ductal carcinoma in situ with lobular carcinoma in situ of breast', 'non-infiltrating ductal and non-infiltrating lobular breast carcinoma', 'non-invasive ductal carcinoma with non-invasive lobular carcinoma of the breast', 'non-invasive ductal carcinoma with non-invasive lobular carcinoma of breast', 'non-invasive ductal and non-invasive lobular breast carcinoma', 'ductal carcinoma in situ with lobular carcinoma in situ of the breast', 'DCIS and LCIS of breast', 'ductal and lobular carcinoma in situ of breast', 'non-infiltrating ductal with non-infiltrating lobular carcinoma of breast', 'intraductal and lobular carcinoma in situ of breast', 'non-invasive ductal and non-invasive lobular carcinoma', 'DCIS and LCIS of the breast', 'non-infiltrating ductal with non-infiltrating lobular carcinoma of the breast', 'intraductal carcinoma and lobular carcinoma in situ', 'non-invasive ductal with non-invasive lobular breast carcinoma', 'non-invasive ductal breast carcinoma with non-invasive lobular breast carcinoma', 'intraductal and lobular carcinoma in situ of the breast', 'ductal and lobular breast carcinoma in situ', 'ductal and lobular carcinoma in situ of the breast', 'intraductal and lobular breast carcinoma in situ']",,,,C0334383,,C4195,1000221,,,,,
mondo:0006186,duodenal adenocarcinoma,"['duodenal adenocarcinoma', 'duodenum adenocarcinoma', 'adenocarcinoma of duodenum', 'adenocarcinoma of the duodenum']",10816,,,C0278804,,C7889,1000223,,,,,
mondo:0006187,duodenal villous adenoma,"['villous adenoma of duodenum', 'villous adenoma of the duodenum', 'duodenum villous adenoma', 'duodenal villous adenoma', 'duodenum adenoma', 'villous adenoma, duodenum']",0050927,,,C1333322,,C5338,1000225,,,,,
mondo:0006188,EBV-positive T-cell lymphoproliferative disorder of childhood,"['EBV-positive T-cell lymphoproliferative disorder of childhood', 'EBV-positive T-cell lymphoproliferative disease of childhood']",,,,C2699838,,C80373,1000228,,,,,
mondo:0006189,eccrine porocarcinoma,"['eccrine porocarcinoma of skin', 'porocarcinoma', 'eccrine porocarcinoma', 'porocarcinoma/spiroadenocarcinoma', 'epidermotropic eccrine carcinoma', 'malignant eccrine poroma']",7566,,,C1266065,,C5560,1000229,D057090,,,,
mondo:0006190,endolymphatic sac tumor,"['endolymphatic sac tumor', 'aggressive papillary tumour of the temporal bone', 'tumour of endolymphatic sac', 'endolymphatic sac tumour (disease)', 'endolymphatic sac tumor (disease)', 'endolymphatic sac neoplasm (disease)', 'neoplasm of endolymphatic sac', 'aggressive papillary tumor of the temporal bone', 'tumor of endolymphatic sac', 'ELST']",,,,C2348239,,C67560,1000230,,212.0,,,0030393
mondo:0006191,endometrial clear cell adenocarcinoma,"['clear cell carcinoma of endometrium', 'clear cell carcinoma of the endometrium', 'endometrium clear cell adenocarcinoma', 'endometrial clear cell adenocarcinoma']",5299,,,C0279765,,C8028,1000231,,,,,
mondo:0006192,endometrial endometrioid adenocarcinoma,"['endometrioid carcinoma of the endometrium', 'endometrioid adenocarcinoma of the endometrium', 'endometrioid carcinoma of endometrium', 'endometrioid endomet. adenocar.', 'endometrioid endometrial adenocarcinoma', 'uterine corpus endometrioid carcinoma', 'endometrial endometrioid adenocarcinoma', 'uterine corpus endometrioid adenocarcinoma', 'uterine endometrioid carcinoma', 'endometrioid adenocarcinoma of endometrium']",,,,C1336905,,C6287,1000233,,,,,
mondo:0006193,endometrial hyperplasia without atypia,['typical endometrial hyperplasia'],,,,,,C40157,1000234,,621.34,,,
mondo:0006195,endometrial polyp,"['endometrial polyp', 'polyp of the endometrium', 'polyp of endometrium', 'polyp, endometrial stromal, benign', 'endometrium polyp', 'endometrial stromal polyp']",,,,,,C6433,1000237,,,,,
mondo:0006196,endometrial serous adenocarcinoma,"['uterine papillary serous carcinoma', 'endometrial serous adenocarcinoma', 'uterine serous papillary adenocarcinoma', 'uterine serous carcinoma', 'uterine serous adenocarcinoma', 'uterine corpus serous adenocarcinoma', 'serous endometrial adenocarcinoma']",,,,,,C27838,1000238,,,,,
mondo:0006197,endometrial small cell carcinoma,"['endometrium small cell carcinoma', 'endometrial small cell carcinoma', 'small cell carcinoma of endometrium']",7139,,,C1516858,,C40155,1000239,,,,,
mondo:0006198,endometrial squamous cell carcinoma,"['squamous cell carcinoma of endometrium', 'endometrium squamous cell carcinoma', 'squamous cell carcinoma of the endometrium', 'endometrial squamous cell carcinoma']",5533,,,C1333396,,C8719,1000240,,,,,
mondo:0006199,endometrial undifferentiated carcinoma,"['undifferentiated endometrial carcinoma', 'endometrial undifferentiated carcinoma']",,,,CN201056,,C40156,1000242,,,,,
mondo:0006200,epithelioid cell uveal melanoma,"['uvea epithelioid cell melanoma', 'epithelioid cell melanoma of uvea', 'epithelioid cell uveal melanoma', 'uveal epithelioid cell melanoma']",7040,,,C1333422,,C35780,1000244,,,,,
mondo:0006201,ethmoid sinus adenoid cystic carcinoma,"['adenoid cystic carcinoma of the ethmoid sinus', 'adenoid cystic carcinoma of ethmoid sinus']",2764,,,C1333473,,C6238,1000246,,,,,
mondo:0006202,extrahepatic bile duct adenosquamous carcinoma,"['adenosquamous bile duct carcinoma', 'adenosquamous carcinoma of bile duct', 'adenosquamous carcinoma of the bile duct', 'bile duct adenosquamous carcinoma', 'extrahepatic bile duct adenosquamous carcinoma']",,,,,,C5778,1000247,,,,,
mondo:0006203,extrahepatic bile duct squamous cell carcinoma,"['bile duct squamous cell carcinoma', 'extrahepatic bile duct squamous cell carcinoma', 'squamous cell bile duct carcinoma', 'squamous cell carcinoma of bile duct', 'squamous cell carcinoma of the bile duct']",,,,C0861861,,C5777,1000248,,,,,
mondo:0006206,fallopian tube carcinoma,"['fallopian tube carcinoma', 'carcinoma of fallopian tube', 'carcinoma of the fallopian tube', 'fallopian tube Ca', 'fallopian tube cancer', 'cancer of the fallopian tube', 'cancer of fallopian tube']",1963,,,C0238122,,C3867,1000251,,,,,
mondo:0006207,fallopian tube carcinosarcoma,"['fallopian tube malignant mixed Mullerian tumour', 'fallopian tube malignant mixed mesodermal (mullerian) tumour', 'fallopian tube carcinosarcoma', 'fallopian tube malignant mixed mesodermal (Müllerian) tumor', 'fallopian tube malignant mixed mesodermal (mullerian) tumor', 'fallopian tube malignant mixed mesodermal (Müllerian) tumour', 'fallopian tube malignant mixed Mullerian tumor']",1970,,,C1517117,,C40124,1000252,,,,,
mondo:0006208,fallopian tube serous adenocarcinoma,['fallopian tube serous adenocarcinoma'],5598,,,C1517124,,C40099,1000253,,,,,
mondo:0006209,fibroblastic neoplasm,"['fibrocytic tumour', 'fibrous tumour', 'fibroblastic tumor', 'fibroblastic tumour', 'fibroblastic neoplasm', 'fibrous neoplasm', 'fibrogenic neoplasm', 'fibrocytic tumor', 'fibrogenicTumor', 'fibrocytic neoplasm', 'fibrous tumor']",,,,,,C7075,1000255,,,,,
mondo:0006210,fibrolamellar hepatocellular carcinoma,"['fibrolamellar hepatocarcinoma', 'fibrolamellar variant of hepatocellular carcinoma', 'eosinophilic glassy cell hepatoma', 'polygonal cell hepatocellular carcinoma with fibrous stroma', 'fibrolamellar carcinoma of the liver cells', 'hepatocellular carcinoma, fibrolamellar', 'fibrolamellar hepatocellular carcinoma', 'oncocytic hepatocellular tumor', 'FLC', 'hepatocellular carcinoma (fibrolamellar variant)', 'fibrolamellar oncocytic hepatoma', 'oncocytic hepatocellular tumour', 'hepatocellular fibrolamellar carcinoma', 'FHCC', 'fibrolamellar cancer', 'fibrolamellar carcinoma of liver cells', 'liver cell fibrolamellar carcinoma', 'eosinophilic hepatocellular carcinoma with lamellar fibrosis', 'hepatocellular carcinoma with increased stromal fibrosis', 'fibrolamellar carcinoma', 'FL-HCC', 'polygonal cell type hepatocellular carcinoma with fibrous Stroma']",5015,,401920,C0334287,,C4131,1000256,C537258,,,,
mondo:0006211,fibrous hamartoma of infancy,"['fibrous hamartoma', 'fibrous hamartoma of infancy', 'infantile fibrous hamartoma']",,,,C0265979,,C3942,1000257,,215.9,,,
mondo:0006212,flat urothelial hyperplasia,['flat urothelial hyperplasia'],,,,,,C27878,1000259,,,,,
mondo:0006213,floor of mouth mucoepidermoid carcinoma,"['mucoepidermoid carcinoma of floor of mouth', 'mouth floor mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the floor of mouth']",,,,C0280310,,C8178,1000260,,,,,
mondo:0006214,follicular variant thyroid gland papillary carcinoma,['FVPTC'],,,,C3714651,,C126594,1000261,,,,,
mondo:0006215,gallbladder adenocarcinoma,"['adenocarcinoma of the gallbladder', 'gall bladder adenocarcinoma', 'gallbladder adenocarcinoma', 'adenocarcinoma of gallbladder']",3500,,,C0279651,,C9166,1000262,,,,,
mondo:0006216,gallbladder adenoma,"['gall bladder adenoma', 'adenoma of gallbladder', 'adenoma of the gallbladder', 'gallbladder adenoma']",0050893,,,C0238137,,C7720,1000263,,,,,
mondo:0006217,gallbladder adenosquamous carcinoma,"['gall bladder adenosquamous carcinoma', 'gallbladder adenosquamous cancer', 'adenosquamous carcinoma of gallbladder', 'adenosquamous carcinoma of the gallbladder', 'GBASC', 'adenosquamous gallbladder carcinoma', 'gallbladder adenosquamous carcinoma']",5627,,,C1333741,,C7356,1000264,,,,,
mondo:0006218,gallbladder biliary intraepithelial neoplasia,"['intracystic biliary intraepithelial neoplasia', 'gallbladder BilIN', 'gallbladder intraepithelial neoplasia', 'intracystic BilIN', 'gallbladder biliary intraepithelial neoplasia', 'gallbladder dysplasia']",,,,C1708174,,C43606,1000265,,,,,
mondo:0006219,gallbladder small cell neuroendocrine carcinoma,"['small cell carcinoma of gall bladder', 'gallbladder small cell NEC', 'gall bladder small cell carcinoma', 'small cell carcinoma of the gallbladder', 'small cell carcinoma of gallbladder', 'gallbladder Oat cell carcinoma', 'gallbladder small cell neuroendocrine carcinoma', 'gallbladder small cell carcinoma', 'Oat cell carcinoma of the gallbladder', 'Oat cell carcinoma of gallbladder']",7133,,,C1333759,,C6763,1000266,,,,,
mondo:0006220,gallbladder squamous cell carcinoma,"['squamous cell carcinoma of gallbladder', 'gall bladder squamous cell carcinoma', 'epidermoid gallbladder carcinoma', 'squamous cell carcinoma of the gallbladder', 'squamous cell gallbladder carcinoma', 'epidermoid carcinoma of gallbladder', 'gallbladder squamous cell carcinoma', 'epidermoid carcinoma of the gallbladder', 'gallbladder squamous cell cancer']",5535,,,C0279658,,C9170,1000267,,,,,
mondo:0006221,gastric adenoma,"['gastric adenoma', 'adenoma of the stomach', 'stomach adenoma', 'adenoma of stomach']",,,,C0149826,,C7699,1000268,,,,,
mondo:0006222,gastric choriocarcinoma,['gastric choriocarcinoma'],,,,C2987398,,C95749,1000269,,,,,
mondo:0006223,gastric diffuse large B-cell lymphoma,"['primary diffuse large B-cell gastric lymphoma', 'primary diffuse large B-cell lymphoma of stomach', 'primary gastric diffuse large B-cell lymphoma', 'gastric diffuse large B-cell lymphoma', 'primary diffuse large B-cell lymphoma of the stomach']",,,,C1335483,,C5253,1000270,,,,,
mondo:0006224,gastric hamartomatous polyp,"['gastric hamartomatous polyp', 'hamartoma of stomach', 'hamartoma of the stomach', 'stomach hamartoma (disease)']",,,,C0341225,,C4373,1000271,,,,,
mondo:0006225,gastric mantle cell lymphoma,"['mantle cell lymphoma of the stomach', 'gastric mantle cell lymphoma', 'stomach mantle cell lymphoma', 'mantle cell lymphoma of stomach']",,,,C1333780,,C27440,1000272,,,,,
mondo:0006226,gastric mucosa-associated lymphoid tissue lymphoma,"['primary gastric B-cell MALT lymphoma', 'gastric MALToma', 'primary MALT lymphoma of the stomach', 'gastric mucosa-associated lymphoid tissue lymphoma', 'MALT lymphoma of stomach', 'MALT lymphoma of the stomach', 'MALToma of the stomach', 'stomach MALT lymphoma', 'primary gastric MALT lymphoma', 'MALToma of stomach', 'gastric MALT lymphoma', 'primary MALT lymphoma of stomach']",,,,C1333782,,C5266,1000274,,,,,
mondo:0006227,gastric neuroendocrine tumor G1,"['gastric enterochromaffin-like cell neuroendocrine tumour', 'gastric enterochromaffin-like cell carcinoid tumor', 'stomach neuroendocrine tumor, well differentiated, low grade', 'gastric enterochromaffin-like cell carcinoid tumour', 'gastric ECL-cell carcinoid tumour', 'stomach NET G1', 'gastric ECL cell, histamine-producing NET', 'stomach carcinoid tumor', 'gastric enterochromaffin-like cell neuroendocrine tumor', 'stomach carcinoid tumour', 'gastric carcinoid tumor', 'gastric carcinoid tumour', 'gastric NET G1', 'gastric ECL cell NET', 'gastric ECL-cell carcinoid tumor', 'gastric ECL cell NET G1', 'grade 1 neuroendocrine neoplasm of stomach']",,,,C0349529,,C4635,1000275,,,,,
mondo:0006228,gastric papillary adenocarcinoma,"['gastric papillary adenocarcinoma', 'papillary stomach adenocarcinoma', 'papillary adenocarcinoma of stomach', 'stomach papillary adenocarcinoma', 'papillary adenocarcinoma of the stomach']",5593,,,C1333785,,C5472,1000276,,,,,
mondo:0006229,gastric small cell neuroendocrine carcinoma,"['stomach small cell carcinoma', 'Oat cell carcinoma of stomach', 'gastric small cell carcinoma', 'small cell carcinoma of the stomach', 'gastric Oat cell carcinoma', 'Oat cell carcinoma of the stomach', 'small cell carcinoma of stomach', 'gastric small cell neuroendocrine carcinoma', 'STSC']",6552,,,C1333788,,C6764,1000277,,,,,
mondo:0006230,gastric squamous cell carcinoma,"['squamous cell carcinoma of stomach', 'gastric squamous cell carcinoma', 'gastric (stomach) squamous cell cancer', 'stomach squamous cell carcinoma', 'squamous cell carcinoma of the stomach']",5516,,418959,CN237470,,C5475,1000278,,,,,
mondo:0006231,gastrointestinal hamartoma,['gastrointestinal hamartoma'],,,,C3272802,,C96475,1000280,,,,,
mondo:0006232,giant cell tumor of soft tissue,"['giant cell tumor of soft tissue', 'GCT-ST', 'Osteoclastoma of soft tissue']",,,,C0334553,,C49107,1000281,,,,,
mondo:0006233,gonadal teratoma,"['gonadal teratoma', 'teratoma, gonads']",,,,C3273942,,C98291,1000282,,,,,
mondo:0006234,grade III prostatic intraepithelial neoplasia,"['carcinoma in situ of prostate', 'carcinoma in situ of prostate gland', 'grade 3 pin', 'prostate adenocarcinoma in situ', 'adenocarcinoma in situ of the prostate', 'pin III', 'adenocarcinoma in situ of prostate', 'grade 3 prostatic intraepithelial neoplasia', 'stage 0 prostate gland carcinoma', 'prostate gland in situ carcinoma', 'grade III pin', 'prostate carcinoma in situ']",8634,,,C0154088,,C3642,1000283,,233.4,D07.5,,
mondo:0006235,granular cell tumor,"['granular cell neoplasm', 'granular cell schwannoma', 'Abrikossoff tumor', 'Abrikosoff^s tumor', 'granular cell tumor', 'GCT', 'Abrikosov^s tumour', 'malignant variant of Abrikosov^s tumour', 'Abrikosoff^s tumour', 'Abrikosov’s tumour', 'granular cell nerve sheath tumor', 'Abrikossoff^s tumour', 'neoplasm of granular cell', 'granular cell myoblastoma', 'giant granulocellular Abrikosov^s tumor', 'granular cell tumour (morphologic abnormality)', 'Abrikosoff^s granulous cell tumour', 'Abrikossoff^s tumor', 'giant granulocellular Abrikosov^s tumour', 'Abrikosov^s tumor', 'Abrikosov’s tumor', 'granular cell tumor NOS (morphologic abnormality)', 'granular cell tumor (morphologic abnormality)', 'Abrikossoff tumour', 'granular cell nerve sheath tumour', 'Abrikosoff^s granulous cell tumor', 'granular cell tumour NOS (morphologic abnormality)', 'malignant variant of Abrikosov^s tumor']",2411,,,C0085167,,C3474,1000284,D016586,215.9,,,
mondo:0006237,granulocytic sarcoma,"['sarcoma, granulocytic, malignant', 'granulocytic sarcoma']",,,,,,C35815,1000286,,,,,
mondo:0006238,growth hormone-producing pituitary gland adenoma,"['growth hormone secreting adenoma of pituitary gland', 'somatotroph adenoma', 'growth hormone producing adenoma of the pituitary gland', 'growth hormone producing adenoma of pituitary gland', 'growth hormone producing pituitary gland adenoma', 'growth hormone secreting pituitary gland adenoma', 'growth hormone producing adenoma of the pituitary', 'growth hormone producing adenoma of pituitary', 'growth hormone-producing pituitary gland adenoma', 'growth hormone-producing adenoma', 'growth hormone secreting adenoma of the pituitary', 'somatotropic adenoma', 'Somatotrophinoma', 'growth hormone secreting adenoma of pituitary', 'growth hormone producing pituitary adenoma', 'GH cell adenoma', 'growth hormone secreting pituitary adenoma', 'growth hormone secreting adenoma of the pituitary gland', 'somatotrope adenoma']",6255,,96256,,"['-0.3203', '0.253', '0.01142', '-0.1888', '0.1179', '0.007053', '0.2041', '0.1356', '-0.1554', '-0.132', '-0.1556', '-0.12115', '0.0774', '0.1781', '-0.09314', '-0.2284', '0.0224', '-0.08734', '-0.1168', '-0.36', '-0.06168', '-0.1383', '0.0919', '-0.2416', '0.2534', '-0.06573', '-0.1326', '-0.2228', '0.01682', '-0.0641', '0.2317', '0.013885', '-0.000298', '-0.08777', '-0.0837', '0.05487', '-0.0681', '0.1576', '-0.02321', '-0.02725', '0.2065', '0.0774', '0.0448', '-0.2025', '0.176', '-0.2404', '-0.01422', '-0.04364', '0.04614', '0.10657', '0.0655', '-0.06836', '-0.10156', '0.273', '-0.3477', '0.05615', '0.2532', '-0.2654', '-0.1494', '0.3208', '0.175', '0.1332', '-0.04724', '0.012886', '-0.108', '0.2068', '0.1903', '0.2367', '-0.2646', '0.1696', '-0.1058', '0.232', '0.2191', '-0.0607', '0.02493', '0.1969', '0.07135', '0.06012', '-0.1555', '-0.19', '-0.1092', '0.2048', '-0.0698', '-0.12427', '-0.1302', '-0.04755', '0.1881', '0.0686', '0.2477', '0.1119', '0.0773', '0.2477', '0.005604', '-0.2212', '0.505', '-0.0763', '0.1725', '-0.2893', '-0.04037', '0.166']",C7461,1000287,,,D35.2,,
mondo:0006239,head and neck paraganglioma,"['craniocervical region paraganglioma', 'paraganglioma of the head and neck', 'paraganglioma of craniocervical region', 'head and neck paraganglioma', 'paraganglioma of head and neck']",,,,C1333944,,C5327,1000288,,,,,
mondo:0006241,hepatic granuloma,,,,,C0745754,,,1000291,,572.8,,,
mondo:0006243,hepatoid adenocarcinoma,"['hepatoid carcinoma', 'hepatoid adenocarcinoma']",0060534,,,C1266090,,C66950,1000293,,,,,
mondo:0006244,HER2 positive breast carcinoma,"['HER2 Positive breast cancer', 'HER2 positive breast carcinoma', 'HER2 Overexpressing subtype of breast carcinoma', 'Her2-receptor positive breast cancer', 'ERBB2 Overexpressing subtype of breast carcinoma', 'HER2 Overexpressing breast carcinoma']",0060079,,,C1960398,,C53556,1000294,,,,,
mondo:0006245,hidradenocarcinoma,"['clear cell eccrine carcinoma', 'hidradenocarcinoma']",,,,,,C54664,1000295,,,,,
mondo:0006246,high grade surface osteosarcoma,"['high-grade surface osteosarcoma', 'high grade surface osteosarcoma']",,,,C1266165,,C53958,1000296,,,,,
mondo:0006247,histiocytic and dendritic cell neoplasm,"['histiocytic and Dendritic cell tumors', 'histiocytic and dendritic cell cancer', 'histiocytic and dendritic cell tumour', 'histiocytic and dendritic cell neoplasm', 'histiocytic and dendritic cell tumor', 'histiocytic and Dendritic cell neoplasms', 'histiocytic and dendritic cell', 'histiocytic and Dendritic cell tumours']",5621,,98287,CN206982,,C9294,1000297,,,,,
mondo:0006248,hydatidiform mole,"['hydatid mole', 'HYDM', 'molar pregnancy', 'hydatidiform mole', 'hydatidiform mole, recurrent']",,,99927,C0020217,"['-0.6753', '0.3643', '-0.3538', '-0.2496', '0.4548', '-0.132', '-0.1262', '0.569', '-0.1293', '0.2654', '-0.3716', '0.4717', '0.001957', '0.4531', '-0.2227', '-0.2039', '0.1766', '0.3608', '0.29', '-0.3186', '-0.265', '-0.2396', '0.415', '-0.5137', '0.1632', '-0.1214', '0.526', '0.1203', '0.03015', '-0.5303', '0.761', '-0.1458', '0.5557', '-0.1243', '-0.3572', '0.705', '0.2163', '-0.0781', '-0.1687', '-0.2087', '0.3708', '0.2612', '0.7163', '-0.2632', '-0.4775', '-0.3655', '-0.591', '-0.4243', '-0.123', '0.2468', '0.356', '-0.114', '-0.01817', '-0.1137', '-0.265', '0.2705', '0.1876', '-0.162', '-0.488', '0.1289', '0.3284', '0.4204', '0.06113', '0.02164', '-0.03506', '0.7983', '0.403', '0.4082', '-0.1104', '0.57', '0.5244', '-0.0528', '-0.1004', '-0.124', '-0.01388', '-0.2224', '0.1066', '0.222', '-0.1321', '-0.1901', '-0.4175', '0.011536', '0.1001', '-0.648', '-0.05502', '-0.1688', '0.3044', '0.3586', '0.4905', '-0.3557', '0.302', '0.397', '-0.2927', '0.1654', '0.1192', '-0.1022', '0.4087', '-0.5825', '0.1472', '0.2927']",C3110,1000298,D006828,631,,10020481,
mondo:0006249,hyperplastic polyp,"['metaplastic polyp', 'MP', 'HP']",,,,C0333983,,C4083,1000299,,,,,
mondo:0006250,ileal neuroendocrine tumor G1,"['ileum neuroendocrine tumor, well differentiated, low grade', 'ileal carcinoid tumor', 'ileum carcinoid tumour', 'ileal neuroendocrine tumor G1', 'ileum carcinoid tumour (disease)', 'ileum carcinoid tumor (disease)', 'ileal carcinoid tumour', 'carcinoid tumor of the ileum', 'carcinoid tumour of the ileum', 'ileum carcinoid tumor', 'grade 1 neuroendocrine neoplasm of ileum', 'ileal NET G1', 'carcinoid tumour of ileum', 'carcinoid tumor of ileum', 'ileum NET G1']",,,,C0745216,,C4935,1000300,,209.03,,,
mondo:0006254,intestinal type adenocarcinoma,"['intestinal-type adenocarcinoma', 'intestinal type carcinoma']",,,,C0334279,,C4126,1000304,,,,,
mondo:0006255,intimal sarcoma,['INTS'],,,,C1708550,,C53677,1000305,,,,,
mondo:0006256,invasive breast carcinoma,"['invasive breast carcinoma', 'infiltrating carcinoma of the breast', 'invasive carcinoma of breast', 'invasive carcinoma of the breast', 'invasive breast cancer', 'infiltrating breast carcinoma', 'infiltrating breast cancer', 'invasive mammary carcinoma', 'infiltrating carcinoma of breast', 'BRCA']",,,,C0853879,,C9245,1000307,,,,,
mondo:0006257,jejunal neuroendocrine tumor G1,"['carcinoid tumor of the jejunum', 'jejunum carcinoid tumour', 'jejunal NET G1', 'jejunum carcinoid tumour (disease)', 'carcinoid tumour of the jejunum', 'grade 1 neuroendocrine neoplasm of jejunum', 'jejunal carcinoid tumour', 'jejunum NET G1', 'jejunum neuroendocrine tumor, well differentiated, low grade', 'jejunum carcinoid tumor', 'jejunum carcinoid tumor (disease)', 'jejunal carcinoid tumor', 'carcinoid tumour of jejunum', 'carcinoid tumor of jejunum']",,,,C1334296,,C6429,1000308,,,,,
mondo:0006258,juvenile polyp,"['retention polyp', 'juvenile polyp']",,,,C0221273,,C3826,1000310,,,,,
mondo:0006260,kidney medullary carcinoma,"['carcinoma of renal medulla', 'renal medullary carcinoma', 'kidney medullary carcinoma']",,,319319,CN203938,,C7572,1000314,,,,10064886,
mondo:0006262,lacrimal gland adenoid cystic carcinoma,"['adenoid cystic carcinoma of the lacrimal gland', 'lacrimal gland adenoid cystic carcinoma', 'adenoid cystic carcinoma of lacrimal gland']",4870,,,C0346340,,C4540,1000317,,,,,
mondo:0006264,laryngeal adenoid cystic carcinoma,"['adenoid cystic carcinoma of larynx', 'adenoid cystic carcinoma of the larynx', 'laryngeal throat adenoid cystic cancer', 'laryngeal adenoid cystic carcinoma']",4869,,,C1334368,,C9462,1000319,,,,,
mondo:0006265,laryngeal small cell carcinoma,"['small cell carcinoma of the larynx', 'larynx small cell carcinoma', 'laryngeal small cell carcinoma', 'small cell carcinoma of larynx', 'laryngeal throat small cell cancer']",7144,,,C1334378,,C6025,1000320,,,,,
mondo:0006266,Leydig cell tumor,"['Leydig cell neoplasm', 'interstitial cell tumour', 'Leydig cell tumor, undetermined', 'Leydig cell tumor', 'interstitial cell neoplasm', 'interstitial cell tumor']",2696,,,C0023601,,C3188,1000321,D007984,,,,
mondo:0006267,liver cavernous hemangioma,"['liver cavernous hemangioma', 'cavernous hemangioma of liver']",,,,C3282904,,C96839,1000322,,,,,
mondo:0006268,liver diffuse large B-cell lymphoma,"['primary liver diffuse large B-cell lymphoma', 'diffuse large B-cell lymphoma of liver', 'liver diffuse large B-cell lymphoma', 'primary hepatic diffuse large B-cell lymphoma', 'hepatic diffuse large B-cell lymphoma']",,,,C2184126,,C96843,1000323,,,,,
mondo:0006270,lobular breast carcinoma in situ,"['LCIS', 'lobular carcinoma in situ of breast', 'lobular carcinoma in situ of the breast (LCIS)', 'non-infiltrating lobular carcinoma', 'non-infiltrating lobular carcinoma of breast', 'non-invasive lobular breast carcinoma', 'non-infiltrating lobular carcinoma of the breast', 'non-infiltrating lobular breast carcinoma', 'non-invasive lobular carcinoma of the breast', 'lobular carcinoma in situ of the breast', 'lobular carcinoma in situ', 'lobular Ca in situ of breast', 'lobular Ca in situ of the breast', 'breast lobular carcinoma in situ', 'non-invasive lobular carcinoma of breast', 'lobular breast carcinoma in situ', 'lobular carcinoma in situ (LCIS)']",,,,C0334381,,C4018,1000326,,,,,
mondo:0006271,low grade central osteosarcoma,"['low grade intramedullary osteosarcoma', 'low-grade intramedullary osteosarcoma', 'intraosseous well-differentiated osteosarcoma', 'low-grade central osteosarcoma', 'intraosseous well-differentiated osteogenic sarcoma', 'low grade central osteosarcoma']",,,,C3814534,,C6474,1000327,,,,,
mondo:0006272,low grade fibromyxoid sarcoma,"['low-grade fibromyxoid sarcoma', 'low grade fibromyxoid sarcoma']",,,,C1275282,,C45202,1000328,,171.9,,,
mondo:0006273,low grade fibromyxoid sarcoma with giant collagen rosettes,"['hyalinizing spindle cell tumor with giant Rosettes', 'hyalinizing spindle cell tumour with giant Rosettes']",,,,C1708749,,C45203,1000329,,,,,
mondo:0006274,low grade vulvar intraepithelial neoplasia,"['grade I vulvar intraepithelial neoplasia', 'VIN 1', 'vulvar Low grade squamous intraepithelial lesion', 'vulva intraepithelial neoplasia grade 1', 'vulvar intraepithelial neoplasia grade 1', 'intraepithelial neoplasia of the vulva grade 1', 'grade 1 vulvar intraepithelial neoplasia', 'VIN grade 1', 'grade I VIN', 'low grade VIN', 'VIN 1 of usual type', 'vulvar Low-grade squamous intraepithelial lesion', 'grade 1 VIN', 'intraepithelial neoplasia of vulva grade 1', 'vulvar intraepithelial neoplasia 1 of usual type', 'vulvar mild squamous dysplasia', 'vulvar flat condyloma']",,,,C0495106,,C4760,1000330,,,,,
mondo:0006275,lung giant cell carcinoma,"['giant cell carcinoma', 'lung giant cell carcinoma', 'giant cell carcinoma of lung', 'giant cell lung carcinoma', 'GCLC', 'giant cell carcinoma of the lung']",5583,,,C0345960,,C4452,1000332,D018286,162.9,,,
mondo:0006276,lung inflammatory myofibroblastic tumor,"['lung inflammatory myofibroblastic tumor', 'inflammatory myofibroblastic lung tumor', 'inflammatory myofibroblastic lung tumour']",,,,C1518038,,C39740,1000333,,,,,
mondo:0006277,lung lymphangioleiomyomatosis,"['lymphangioleiomyomatosis', 'lung lymphangioleiomyomatosis', 'pulmonary lymphangiomyomatosis', 'lung lymphangiomyomatosis']",3319,,538,,"['-0.2847', '0.1776', '-0.3948', '-0.4785', '-0.4082', '-0.0902', '0.6953', '-0.1571', '-0.16', '-0.1719', '-0.07996', '0.2927', '-0.2406', '0.618', '0.349', '-0.2388', '-0.4055', '0.003332', '0.0256', '-0.862', '-0.6445', '-0.4976', '0.6177', '-0.5405', '-0.2185', '-0.1367', '0.013466', '-0.01393', '0.366', '0.284', '0.729', '-0.2708', '0.929', '0.311', '0.0931', '-0.5215', '-0.3462', '0.136', '0.75', '0.5874', '0.08765', '0.1963', '0.7285', '-0.2625', '0.263', '0.3335', '-1.002', '-0.3733', '-0.0827', '0.1138', '-0.06134', '0.3972', '0.2627', '-0.0913', '-0.5586', '-0.1743', '0.0876', '-0.506', '-0.6987', '0.0892', '0.8154', '0.6714', '0.3713', '-0.07135', '0.03485', '-0.0524', '1.065', '0.1337', '-0.1156', '0.7305', '0.1226', '-0.387', '-0.163', '-0.6226', '0.2922', '-0.438', '0.3406', '0.012985', '0.0465', '-0.4373', '-0.6367', '-0.1351', '0.3691', '0.11835', '-0.55', '-0.1744', '0.1926', '-0.04855', '-0.2183', '-0.0462', '0.302', '0.10297', '-0.6396', '0.000436', '0.848', '-0.196', '0.416', '-0.4192', '-0.1924', '0.254']",C38153,1000334,,518.89,,10049459,
mondo:0006278,lung papilloma,"['papilloma of the respiratory tract', 'respiratory tract papilloma', 'papilloma of respiratory tract', 'lung papilloma']",,,,C0281373,,C8295,1000335,,,,,
mondo:0006279,lung sarcomatoid carcinoma,"['sarcomatoid carcinoma of the lung', 'lung sarcomatoid carcinoma']",0080777,,,,,C45540,1000336,,162.9,,,
mondo:0006280,lung sclerosing hemangioma,"['sclerosing Pneumocytoma', 'sclerosing hemangioma of lung', 'pulmonary sclerosing hemangioma', 'sclerosing hemangioma', 'sclerosing haemangioma', 'sclerosing hemangioma of the lung', 'lung sclerosing angioma', 'Pneumocytoma', 'sclerosing angioma of the lung', 'sclerosing angioma of lung', 'lung sclerosing hemangioma']",5766,,,C1509148,,C5656,1000337,D047868,228.09,,,
mondo:0006281,lung signet ring cell carcinoma,"['signet ring lung adenocarcinoma', 'lung signet ring cell carcinoma']",0080305,,,,,C45514,1000338,,162.9,,,
mondo:0006282,lymphangiosarcoma,"['lymphangiosarcoma', 'lymphangiosarcoma, malignant', 'lymphangiosarcoma of Stewart and Treves', 'Stewart-Treves syndrome', 'malignant lymphangioendothelioma', 'lymphangioendothelial sarcoma']",2689,,,C0024224,,C3205,1000339,D008204,171.9,,,
mondo:0006283,lymphoepithelioma-like lung carcinoma,['lymphoepithelioma-like carcinoma of the lung'],,,,C1708792,,C45519,1000340,,,,,
mondo:0006284,major salivary gland carcinoma,"['carcinoma of Major salivary gland', 'major salivary gland carcinoma', 'carcinoma of the major salivary gland', 'carcinoma of major salivary gland', 'major salivary gland cancer']",,,,C1334549,,C5907,1000344,,,,,
mondo:0006285,major salivary gland carcinoma ex pleomorphic adenoma,"['carcinoma ex pleomorphic adenoma of the Major salivary gland', 'major salivary gland salivary gland carcinoma ex pleomorphic adenoma', 'major salivary gland carcinoma ex pleomorphic adenoma', 'carcinoma ex pleomorphic adenoma of Major salivary gland']",,,,C1334550,,C5975,1000345,,,,,
mondo:0006286,major salivary gland mucoepidermoid carcinoma,"['major salivary gland mucoepidermoid cancer', 'mucoepidermoid carcinoma of Major salivary gland', 'mucoepidermoid carcinoma of the Major salivary gland', 'major salivary gland mucoepidermoid carcinoma']",,,,C1334551,,C5906,1000346,,,,,
mondo:0006287,malignancy in giant cell tumor of bone,"['malignancy in giant cell tumour of the bone', 'giant cell tumour of bone, malignant (morphologic abnormality)', 'giant cell tumour of bone, malignant', 'malignancy in giant cell tumor of bone', 'giant cell tumor of bone, malignant', 'malignant giant cell tumor of bone', 'Dedifferentiated giant cell tumor', 'malignancy in giant cell tumor of the bone', 'Dedifferentiated giant cell tumour', 'giant cell tumor of bone, malignant (morphologic abnormality)', 'giant cell bone sarcoma', 'OSTEOCLASTOMA, malignant', 'giant cell sarcoma of bone', 'giant cell sarcoma of the bone', 'malignant giant cell tumour of bone', 'bone giant cell sarcoma']",4719,,,C0334552,,C4304,1000347,,,,,
mondo:0006288,malignant adrenal gland pheochromocytoma,"['malignant adrenal gland paraganglioma', 'malignant adrenal medullary pheochromocytoma', 'malignant adrenal gland chromaffin tumor', 'pheochromocytoma, malignant', 'malignant adrenal gland chromaffin paraganglioma', 'malignant adrenal gland chromaffin tumour', 'malignant pheochromocytoma', 'pheochromoblastoma', 'malignant adrenal gland pheochromocytoma', 'adrenal gland pheochromocytoma, malignant', 'malignant adrenal gland Chromaffinoma', 'malignant adrenal gland chromaffin neoplasm', 'malignant adrenal pheochromocytoma', 'malignant adrenal medullary paraganglioma']",0080347,,,C0334419,,C4220,1000348,,,,,
mondo:0006290,malignant germ cell tumor,"['malignant germ cell tumor', 'malignant neoplasm of the germ cell', 'malignant neoplasm of germ cell', 'malignant tumor of germ cell', 'malignant tumour of germ cell', 'malignant germ cell neoplasm', 'malignant tumour of the germ cell', 'germ cell tumor, malignant', 'germ cell cancer', 'cancer of germ cell', 'malignant tumor of the germ cell']",,,,C4048549,,C4925,1000352,,,,,
mondo:0006291,malignant jugulotympanic paraganglioma,"['malignant glomus jugulare neoplasm', 'malignant glomus jugulare tumour', 'malignant tumor of glomus jugulare', 'jugular body cancer', 'malignant tumour of the glomus jugulare', 'malignant jugular body neoplasm', 'malignant tumour of glomus jugulare', 'malignant neoplasm of jugular body', 'malignant tumor of the glomus jugulare', 'malignant neoplasm of the glomus jugulare', 'malignant glomus jugulare tumor', 'malignant jugulotympanic paraganglioma', 'malignant neoplasm of glomus jugulare', 'cancer of jugular body']",,,,C0347856,,C4623,1000353,,,,,
mondo:0006292,malignant mesothelioma,"['mesothelioma, malignant', 'MESOM', 'malignant mesothelial tumour', 'mesothelioma, somatic', 'asbestos-related malignant mesothelioma', 'malignant tumour of the mesothelium', 'malignant mesothelial tumor', 'diffuse malignant mesothelioma', 'advanced malignant mesothelioma', 'malignant mesothelioma (disease)', 'malignant neoplasm of mesothelium', 'malignant tumor of the mesothelium', 'malignant mesothelial neoplasm', 'malignant tumor of mesothelium', 'malignant mesothelioma', 'malignant neoplasm of the mesothelium', 'malignant tumour of mesothelium']",1790,156240,50251,C1332338,"['0.3315', '0.05722', '0.1969', '0.0546', '0.03528', '0.5396', '0.009155', '0.6187', '-0.4983', '-0.1385', '0.757', '0.2617', '-0.2286', '0.00699', '-0.4583', '0.06125', '-0.9375', '-0.5454', '-0.1682', '-0.3801', '0.0924', '-0.7065', '0.642', '-0.167', '-0.2372', '-0.5244', '-0.2367', '0.7173', '0.3484', '0.04465', '0.562', '-0.1733', '0.825', '-0.1943', '0.4705', '-0.4575', '-0.996', '0.4585', '0.817', '-0.1012', '0.03287', '-0.01186', '0.533', '-0.4316', '-0.1964', '0.4204', '-0.1306', '-0.03976', '0.6304', '0.0085', '0.07416', '-0.711', '0.1272', '-0.02477', '0.2568', '0.3315', '-0.3884', '0.4026', '-0.5967', '-0.4958', '0.5215', '0.261', '-0.709', '0.1898', '-0.1289', '0.75', '0.1254', '0.7344', '-0.4243', '0.7637', '-0.2439', '0.1841', '0.05225', '-0.2837', '0.8354', '0.6387', '-0.168', '0.3584', '0.11017', '-0.399', '-0.3804', '0.204', '-0.1798', '0.05762', '0.03062', '0.003565', '0.6357', '0.633', '0.4678', '-0.1125', '-0.06097', '-0.754', '-0.904', '0.7627', '0.899', '-0.2354', '-0.002638', '-0.1909', '-0.4656', '-0.0455']",C4456,1000355,C562839,199.1,,10027406,0100001
mondo:0006294,pleural cancer,"['malignant neoplasm of pleura', 'cancer of the pleura', 'malignant tumor of pleura', 'malignant tumour of the pleura', 'neoplasm of pleura', 'cancer of pleura', 'malignant tumor of the pleura', 'pleural cancer', 'malignant pleural neoplasm', 'malignant pleura neoplasm', 'malignant tumour of pleura', 'malignant pleural tumor', 'malignant pleural tumour', 'pleura cancer', 'pleural tumour', 'pleural tumor', 'malignant neoplasm of the pleura']",5158,,,C0153494,,C3547,1000362,,163.9,C38.4,,
mondo:0006295,malignant urinary system neoplasm,"['cancer of renal system', 'malignant renal system neoplasm', 'malignant neoplasm of renal system', 'urinary system cancer', 'malignant urinary system neoplasm', 'renal system cancer', 'malignant urinary tract neoplasm']",3996,,,,,C9297,1000363,,189.9,C64-C68,,
mondo:0006297,maxillary sinus adenoid cystic carcinoma,"['adenoid cystic carcinoma of the maxillary sinus', 'adenoid cystic carcinoma of maxillary sinus', 'maxillary sinus adenoid cystic carcinoma']",7198,,,C1334643,,C6239,1000365,,,,,
mondo:0006298,mediastinal malignant germ cell tumor,"['malignant germ cell neoplasm of the mediastinum', 'malignant mediastinal germ cell tumour', 'thymic malignant germ cell tumour', 'malignant germ cell tumour of mediastinum', 'malignant germ cell tumour of the mediastinum', 'mediastinal germ cell tumor, malignant', 'thymic malignant germ cell tumor', 'malignant germ cell tumor of the mediastinum', 'malignant mediastinal germ cell neoplasm', 'malignant germ cell neoplasm of mediastinum', 'malignant germ cell tumor of mediastinum', 'mediastinal malignant germ cell tumor']",,,,C1334597,,C6446,1000366,,,,,
mondo:0006300,medullomyoblastoma with myogenic differentiation,"['medullomyoblastoma', 'MMB', 'medullomyoblastoma with myogenic differentiation']",3861,,,C0205833,,C3706,1000368,,,,,
mondo:0006301,metanephric adenoma,"['metanephric adenoma (morphologic abnormality)', 'metanephric adenoma']",6404,,,C1266045,,C27253,1000373,,,,,
mondo:0006302,micropapillary serous carcinoma,,,,,,,C6882,1000377,,,,,
mondo:0006303,middle ear squamous cell carcinoma,"['epidermoid carcinoma of the middle Ear', 'squamous cell carcinoma of middle ear', 'epidermoid carcinoma of the middle ear', 'epidermoid carcinoma of middle Ear', 'middle ear squamous cell carcinoma', 'squamous cell carcinoma of middle Ear', 'middle Ear epidermoid carcinoma', 'squamous cell carcinoma of the middle Ear']",5526,,,C1334762,,C6086,1000378,,,,,
mondo:0006304,minor salivary gland adenocarcinoma,"['adenocarcinoma of minor salivary gland', 'adenocarcinoma of the minor salivary gland']",,,,C1334768,,C5948,1000379,,,,,
mondo:0006306,mixed lobular and ductal breast carcinoma,"['mixed ductal and lobular breast carcinoma', 'ductal and lobular carcinoma', 'mixed lobular and ductal carcinoma of breast', 'mixed ductal and lobular carcinoma of breast', 'mixed lobular and ductal carcinoma', 'breast mixed ductal and lobular carcinoma', 'mixed lobular and ductal carcinoma of the breast', 'mixed lobular and ductal breast carcinoma', 'mixed ductal and lobular carcinoma of the breast']",,,,C0334384,,C5160,1000382,,174.8,,,
mondo:0006307,mixed somatotroph-lactotroph pituitary gland adenoma,"['Mixed somatotroph and lactotroph adenoma', 'mixed Somatolactotrope adenoma', 'mixed GH-PRL cell adenoma', 'mixed somatotroph-lactotroph pituitary gland adenoma', 'mixed somatotroph-lactotroph adenoma']",,,,C1709052,,C45927,1000383,,,,,
mondo:0006309,mucinous gastric adenocarcinoma,"['mucinous stomach adenocarcinoma', 'mucinous adenocarcinoma of stomach', 'MSTAD', 'mucinous gastric adenocarcinoma', 'mucinous adenocarcinoma of the stomach', 'stomach mucinous adenocarcinoma']",3716,,,C1334809,,C5248,1000386,,,,,
mondo:0006311,myelodysplastic/myeloproliferative neoplasm,"['MPD-MDS', 'myelodysplastic/myeloproliferative disorder', 'myelodysplastic myeloproliferative disease', 'myelodysplastic/myeloproliferative disorders', 'myelodysplastic/myeloproliferative neoplasm', 'MDS/MPD', 'MPD/MDS', 'myelodysplastic/myeloproliferative neoplasms', 'myelodysplastic/myeloproliferative diseases', 'MDS-MPD', 'myeloproliferative/myelodysplastic syndromes', 'MDS/MPN', 'myelodysplastic/myeloproliferative disease', 'myelodysplastic myeloproliferative cancer', 'myeloproliferative/myelodysplastic disorders']",4972,,,,,C27262,1000388,D054437,,,,
mondo:0006312,myofibroma,"['myofibroma', 'infantile hemangiopericytoma', 'myofibroma (morphologic abnormality)', 'lipoleiomyoma']",4386,,,C1266121,,C7052,1000389,D047708,,,,
mondo:0006313,nabothian cyst,,,,,C0027269,,C34835,1000390,,,,,
mondo:0006314,nasal cavity polyp,"['nasal cavity polyp', 'nasal polyp', 'polyp of the nasal cavity', 'polyp of nasal cavity']",,,,C0027430,,C3256,1000391,D009298,471.9,,,
mondo:0006316,neuroblastic tumor,['neuroblastic tumor'],,,,C1334953,,C6963,1000393,,,,,
mondo:0006317,neurothekeoma,"['neurothekeoma', 'nerve sheath Myxoma']",,,,C0206730,,C7018,1000394,D018321,,,,
mondo:0006320,non-cutaneous melanoma,"['non-cutaneous melanoma', 'extracutaneous melanoma']",,,,C1334974,,C8711,1000397,,,,,
mondo:0006321,non-functioning adrenal cortex adenoma,"['non-functioning adrenal cortical adenoma', 'adrenal cortical incidentaloma', 'non-functioning adrenal cortex adenoma', 'adrenal cortex non-functioning endocrine neoplasm', 'non-functioning endocrine neoplasm of adrenal cortex', 'nonfunctional adrenal cortex adenoma']",,,,C1709240,,C48458,1000399,,,,,
mondo:0006322,non-neoplastic bile duct disorder,['non-neoplastic bile duct disorder'],,,,C3275160,,C35774,1000400,,,,,
mondo:0006323,non-seminomatous lesion,,,,,,,,1000401,,,,,
mondo:0006324,normal breast-like subtype of breast carcinoma,"['normal breast-like subtype of breast cancer', 'normal breast-like subtype of breast carcinoma']",,,,C3642471,,C53557,1000402,,,,,
mondo:0006325,ocular melanoma,"['OM', 'eye melanoma', 'melanoma of the eye', 'eye melanoma (disease)', 'ocular melanoma', 'melanoma of eye', 'eyeball of camera-type eye melanoma (disease)']",1752,,,,,C8562,1000403,,,,,
mondo:0006326,ocular melanoma with extraocular extension,"['extraocular extension of melanoma', 'ocular melanoma with extraocular extension', 'extraocular extension melanoma']",,,,C0278869,,C7913,1000404,,,,,
mondo:0006327,ocular sebaceous carcinoma,"['eye sebaceous carcinoma', 'ocular sebaceous carcinoma']",,,,C1709308,,C43340,1000405,,,,,
mondo:0006328,odontogenic cyst,,,,,,,C54220,1000406,D009807,526.89,,,
mondo:0006329,olfactory neuroblastoma,"['paranasal sinus olfactory neuroblastoma', 'Asthesioneuroblastoma', 'Esthesioneuroepithelioma [dup] (morphologic abnormality)', 'esthesioneuroblastoma', 'Esthesioneuroepithelioma', 'Asthesioneuroblastoma (morphologic abnormality)', 'olfactory neuroblastoma', 'Esthesioneuroepithelioma (morphologic abnormality)', 'olfactory neuroepithelioma', 'esthesioneuroblastoma (morphologic abnormality)', 'olfactory esthesioneuroblastoma']",369,,,,,C3789,1000407,,,,,
mondo:0006330,ossifying fibromyxoid tumor,"['ossifying fibromyxoid tumor (morphologic abnormality)', 'OFMT', 'ossifying fibromyxoma', 'ossifying fibromyxoid neoplasm', 'ossifying fibromyxoid tumour (morphologic abnormality)']",2685,,,C1266128,,C6582,1000408,,,,,
mondo:0006335,ovarian endometrioid adenocarcinoma,"['ovarian endometrioid adenocarcinoma', 'endometrioid cancer of the ovary', 'endometrioid cancer of ovary', 'endometrioid ovarian cancer', 'ovarian endometrioid cancer', 'ovarian endometrioid carcinoma', 'endometrium adenocarcinoma of ovary', 'ovary endometrium adenocarcinoma', 'endometrioid carcinoma of ovary', 'endometrioid adenocarcinoma of ovary', 'endometrioid carcinoma of the ovary', 'endometrioid adenocarcinoma of the ovary', 'endometrioid carcinoma ovary', 'endometrioid ovary carcinoma']",5828,,454723,C0346163,,C7979,1000416,,,,,
mondo:0006336,ovarian endometrioid adenocarcinoma with squamous differentiation,"['ovarian adenoacanthoma', 'ovarian adenosquamous carcinoma', 'ovarian endometrioid adenocarcinoma with squamous differentiation']",,,,,,C40061,1000417,,,,,
mondo:0006337,ovarian endometriosis,"['ovarian endometriosis', 'ovary endometriosis (disease)', 'endometriosis of ovary']",11432,,,C0156344,,C27628,1000418,,617.1,N80.1,,
mondo:0006339,ovarian microcystic stromal tumor,"['microcystic stromal tumor', 'MCST', 'microcystic stromal tumour']",,,569248,C4054287,,C121953,1000424,,,,,
mondo:0006340,ovarian serous adenofibroma,"['ovary serous adenofibroma', 'serous adenofibroma of ovary', 'ovarian serous adenofibroma']",5474,,,C1518729,,C40031,1000428,,,,,
mondo:0006343,ovarian transitional cell carcinoma,"['malignant ovarian transitional cell neoplasm', 'ovarian transitional cell carcinoma', 'transitional cell carcinoma of ovary', 'ovarian transitional cell cancer', 'ovary transitional cell carcinoma', 'ovarian transitional cell neoplasm', 'transitional cell carcinoma of the ovary']",4000,,,C1335184,,C5240,1000435,,,,,
mondo:0006344,ovarian yolk sac tumor,"['ovarian yolk Sac neoplasm', 'germ cell endodermal sinus tumour of the ovary', 'ovarian germ cell endodermal sinus tumor', 'yolk Sac neoplasm of the ovary', 'germ cell endodermal sinus tumor of ovary', 'germ cell endodermal sinus tumour of ovary', 'endodermal sinus neoplasm of ovary', 'yolk sac tumour', 'germ cell endodermal sinus neoplasm of the ovary', 'ovarian endodermal sinus tumor', 'endodermal sinus tumor of the ovary', 'yolk Sac tumour of ovary', 'ovarian germ cell endodermal sinus tumour', 'ovarian endodermal sinus tumour', 'yolk Sac neoplasm of ovary', 'ovarian germ cell endodermal sinus neoplasm', 'endodermal sinus tumor of ovary', 'endodermal sinus tumour of the ovary', 'endodermal sinus neoplasm of the ovary', 'ovarian endodermal sinus neoplasm', 'endodermal sinus tumour of ovary', 'ovary yolk sac tumor', 'ovary yolk sac tumour', 'yolk Sac tumor of the ovary', 'yolk sac tumor', 'germ cell endodermal sinus neoplasm of ovary', 'ovarian yolk sac tumor', 'yolk Sac tumor of ovary', 'yolk Sac tumour of the ovary', 'germ cell endodermal sinus tumor of the ovary']",5350,,,C0346188,,C8107,1000437,,,,,
mondo:0006345,palmar fibromatosis,"['Dupuytren^s contracture', 'palmar part of manus fibromatosis', 'Dupuytren contracture', 'palmar fibromatosis', 'Dupuytren contracture (disease)']",,,,,,C3469,1000438,D004387,,,,0005679
mondo:0006346,pancreatic acinar cell carcinoma,"['acinar cell adenocarcinoma of the pancreas', 'Pancreatic acinar cell cancer', 'acinar cell carcinoma of the pancreas', 'pancreatic acinar cell carcinoma', 'carcinoma of pancreatic acinar cell', 'acinar cell carcinoma of pancreas', 'pancreas acinar cell adenocarcinoma', 'PAAC', 'acinar cell adenocarcinoma of pancreas', 'pancreatic acinar cell adenocarcinoma']",5742,,424046,C0279661,,C7977,1000439,,,,,
mondo:0006347,pancreatic large cell neuroendocrine carcinoma,"['pancreatic large cell NEC G3', 'pancreatic large cell neuroendocrine carcinoma', 'pancreas large cell neuroendocrine carcinoma', 'pancreatic large cell NEC', 'large cell neuroendocrine carcinoma of pancreas']",,,,C2987239,,C95582,1000442,,,,,
mondo:0006348,pancreatic small cell neuroendocrine carcinoma,"['pancreatic small cell NEC G3', 'endocrine pancreas small cell carcinoma', 'pancreatic small cell NEC', 'small cell carcinoma of endocrine pancreas', 'pancreatic small cell neuroendocrine carcinoma']",,,,C2987240,,C95583,1000444,,,,,
mondo:0006349,papillary cystic neoplasm,"['papillary cystic tumour', 'papillary cystic neoplasm', 'papillary cystic tumor']",,,,C0334357,,C4179,1000448,,,,,
mondo:0006350,papillary transitional cell carcinoma,"['papillary transitional carcinoma', 'papillary transitional cell carcinoma', 'papillary transitional cell carcinoma (morphologic abnormality)']",4012,,,C0334274,,C4122,1000450,,,,,
mondo:0006351,parachordoma,['parachordoma'],2647,,,C1266175,,C6581,1000452,,,,,
mondo:0006352,paranasal sinus adenoid cystic carcinoma,"['adenoid cystic carcinoma of the accessory sinus', 'adenoid cystic carcinoma of accessory sinus', 'adenoid cystic carcinoma of paranasal sinus', 'paranasal sinus adenoid cystic carcinoma', 'accessory sinus adenoid cystic carcinoma', 'adenoid cystic carcinoma of the paranasal sinus']",,,,C1335337,,C6019,1000454,,,,,
mondo:0006353,paranasal sinus Schneiderian papilloma,"['Schneiderian papilloma of the paranasal sinus', 'Schneiderian papilloma of the accessory sinus', 'accessory sinus Schneiderian papilloma', 'Schneiderian papilloma of paranasal sinus', 'paranasal sinus Schneiderian papilloma', 'Schneiderian papilloma of accessory sinus']",,,,C1335343,,C6835,1000455,,,,,
mondo:0006354,parathyroid hyperplasia,"['parathyroid hyperplasia', 'hyperplasia of parathyroid', 'parathyroid gland hyperplasia', 'parathyroid hyperplasia (disease)', 'hyperplasia of the parathyroid']",,,,C0271844,,C3989,1000457,,,,,0008208
mondo:0006355,parotid gland acinic cell carcinoma,"['parotid gland acinic cell carcinoma', 'acinic cell carcinoma of parotid', 'acinic cell carcinoma of parotid gland', 'parotid acinic cell carcinoma', 'acinic cell carcinoma of the parotid', 'parotid gland acinar cell carcinoma', 'acinic cell carcinoma of the parotid gland']",,,,C1335353,,C5933,1000458,,,,,
mondo:0006356,parotid gland adenoid cystic carcinoma,"['adenoid cystic carcinoma of the parotid', 'parotid adenoid cystic carcinoma', 'adenoid cystic carcinoma of parotid gland', 'parotid gland adenoid cystic carcinoma', 'adenoid cystic carcinoma of parotid', 'adenoid cystic carcinoma of the parotid gland']",0050931,,,C1335355,,C5937,1000459,,,,,
mondo:0006357,parotid gland carcinoma ex pleomorphic adenoma,"['carcinoma ex pleomorphic adenoma of the parotid', 'carcinoma ex pleomorphic adenoma of the parotid gland', 'parotid gland carcinoma ex pleomorphic adenoma', 'carcinoma ex pleomorphic adenoma of parotid gland', 'carcinoma ex pleomorphic adenoma of parotid', 'parotid carcinoma ex pleomorphic adenoma']",,,,C1335356,,C5974,1000461,,,,,
mondo:0006358,parotid gland squamous cell carcinoma,"['squamous cell carcinoma of the parotid', 'squamous cell carcinoma of the parotid gland', 'squamous cell carcinoma of parotid', 'parotid squamous cell carcinoma', 'squamous cell carcinoma of parotid gland', 'parotid gland squamous cell carcinoma']",,,,C1335367,,C5942,1000463,,,,,
mondo:0006359,neoplasm with perivascular epithelioid cell differentiation,"['tumour with perivascular epithelioid cell differentiation', 'neoplasm with perivascular epithelioid cell differentiation', 'tumor with perivascular epithelioid cell differentiation', 'perivascular epithelioid cell tumour', 'perivascular epithelioid cell tumor', 'PEComa']",2643,,595133,C1300127,,C38150,1000464,D054973,,,,
mondo:0006360,penile carcinoma,"['cancer of the penis', 'cancer penis', 'cancer of penis', 'carcinoma of the penis', 'penis carcinoma', 'penile cancer, adult', 'carcinoma of penis', 'penile carcinoma', 'penile cancer']",3449,,,,,C9061,1000465,,,,,
mondo:0006361,penile fibromatosis,"['penis fibromatosis', 'penile fibromatosis', 'Peyronie^s fibromatosis', 'Peyronie^s disease', 'penile induration']",,,,C0030848,,C3316,1000466,,,,,
mondo:0006362,peritoneal mesothelioma,"['peritoneal mesothelioma (disease)', 'mesothelioma of peritoneum', 'peritoneal mesothelioma', 'peritoneum mesothelioma', 'mesothelioma of the peritoneum']",,,,,,C7633,1000467,,,,,0100003
mondo:0006363,peritoneal multicystic mesothelioma,"['peritoneal multicystic mesothelioma', 'multicystic mesothelioma', 'peritoneal cystic mesothelioma', 'benign cystic peritoneal mesothelioma', 'multilocular peritoneal inclusion cysts', 'multicystic mesothelioma of the peritoneum', 'multilocular peritoneal inclusion cyst', 'multicystic mesothelioma of peritoneum', 'multilocular peritoneal cysts', 'BMPM', 'benign multicystic peritoneal mesothelioma']",,,168816,C1334818,,C6536,1000468,,,,,
mondo:0006364,peritoneal well differentiated papillary mesothelioma,"['peritoneal WDPM', 'peritoneal well differentiated papillary mesothelioma']",,,,C1709507,,C45661,1000469,,,,,
mondo:0006365,Peutz-Jeghers polyp,"['Peutz Jeghers polyp', 'Peutz-Jeghers polyp']",,,,,,C4733,1000470,,,,,
mondo:0006366,Peutz-Jeghers polyp of the stomach,['Gastric Peutz-Jeghers polyp'],,,,C1335398,,C36205,1000471,,,,,
mondo:0006367,pharyngeal adenoid cystic carcinoma,"['pharynx adenoid cystic carcinoma', 'pharyngeal throat adenoid cystic cancer', 'pharyngeal adenoid cystic carcinoma', 'adenoid cystic carcinoma of pharynx', 'adenoid cystic carcinoma of the pharynx']",,,,C1335399,,C5818,1000472,,,,,
mondo:0006368,phosphaturic mesenchymal tumor,"['phosphaturic mesenchymal tumor, mixed connective tissue variant', 'phosphaturic mesenchymal tumor', 'phosphaturic mesenchymal tumor, mixed connective tissue type']",,,,C1831619,,C67237,1000473,,,,,
mondo:0006369,pineal parenchymal tumor of intermediate differentiation,"['pineal parenchymal tumor of intermediate differentiation (morphologic abnormality)', 'pineal parenchymal tumor of intermediate differentiation', 'pineal parenchymal tumors of intermediate differentiation', 'pineal parenchymal tumours of intermediate differentiation', 'pineal parenchymal tumour of intermediate differentiation (morphologic abnormality)', 'PPTID']",5030,,,C1367859,,C6967,1000474,,,,,
mondo:0006372,pituicytoma,"['pituicytoma', 'posterior pituitary astrocytoma', 'pituicytoma (WHO grade I)', 'PTCY']",0081280,,251623,C2986550,,C94524,1000477,,237.0,,,
mondo:0006373,pituitary gland adenoma,"['pituitary gland adenoma', 'PTAD', 'adenoma of pituitary', 'adenoma of pituitary gland', 'adenoma of the pituitary', 'adenoma, anterior lobe pituitary gland, benign', 'adenoma of the pituitary gland', 'pituitary adenoma']",3829,,99408,C0032000,"['-0.4358', '0.04587', '0.08344', '0.1583', '0.08636', '0.1364', '0.2732', '0.0443', '-0.4644', '-0.1056', '-0.4187', '-0.1669', '0.03568', '0.0804', '-0.03284', '-0.365', '-0.10974', '-0.4456', '-0.192', '-0.3706', '0.1133', '-0.174', '0.294', '-0.194', '0.3213', '-0.07764', '-0.1652', '0.1556', '-0.2073', '0.2766', '0.397', '-0.07513', '0.2568', '-0.2864', '0.0763', '-0.02057', '0.06647', '0.1125', '0.0886', '-0.3113', '0.3735', '0.01924', '0.2898', '-0.098', '0.266', '-0.00565', '0.121', '-0.07324', '0.06836', '0.0332', '0.2229', '0.05118', '-0.05655', '0.3347', '-0.3264', '0.358', '0.4536', '-0.247', '-0.3362', '0.2454', '-0.02524', '0.00953', '-0.04684', '0.0547', '-0.1785', '0.272', '0.3552', '0.4788', '-0.0332', '0.1971', '-0.03976', '0.3572', '0.3552', '-0.1676', '-0.1328', '-0.00872', '0.2505', '-0.1382', '-0.04837', '-0.678', '-0.1699', '0.1278', '0.00888', '0.2996', '-0.269', '-0.0689', '0.0635', '0.03622', '0.2864', '0.0868', '0.00933', '0.126', '0.03876', '-0.079', '0.581', '-0.299', '0.2327', '-0.02727', '-0.04395', '0.3542']",C3329,1000478,,,D35.2,10035079,
mondo:0006374,placental choriocarcinoma,"['placenta choriocarcinoma', 'choriocarcinoma of placenta', 'choriocarcinoma of the placenta', 'placenta choriocarcinoma (disease)', 'placental choriocarcinoma']",2024,,,C0855173,,C8893,1000479,,,,,
mondo:0006375,placental hemangioma,"['chorioangioma', 'placenta hemangioma', 'placental hemangioma', 'hemangioma of the placenta', 'angioma of placenta', 'Chorangioma', 'hemangioma of placenta', 'Chorangioma of the placenta', 'Chorangioma placentae', 'placental angioma', 'angioma of the placenta']",277,,,C0677608,,C4868,1000480,,219.8,,,
mondo:0006377,pleural biphasic mesothelioma,['pleural biphasic mesothelioma'],,,,C1709570,,C45665,1000483,,,,,
mondo:0006378,pleural epithelioid mesothelioma,"['pleura malignant epithelioid mesothelioma', 'pleural epithelioid mesothelioma', 'malignant epithelioid mesothelioma of pleura']",,,,C1709574,,C45662,1000484,,,,,
mondo:0006380,pleural sarcomatoid mesothelioma,"['pleura sarcomatoid mesothelioma', 'sarcomatoid mesothelioma of pleura', 'pleural sarcomatoid mesothelioma']",,,,C1709578,,C45663,1000486,,,,,
mondo:0006381,plexiform ameloblastoma,,,,,C0457529,,C39753,1000487,,,,,
mondo:0006382,poorly differentiated thyroid gland carcinoma,"['poorly differentiated thyroid carcinoma', 'insular carcinoma', 'poorly differentiated thyroid gland carcinoma', 'poorly differentiated thyroid cancer', 'poorly differentiated carcinoma of thyroid gland', 'thyroid gland poorly differentiated carcinoma', 'poorly differentiated thyroid gland cancer', 'poorly differentiated carcinoma of the thyroid gland']",,,,C1266050,,C6040,1000489,,,,,
mondo:0006383,"primary cutaneous diffuse large B-cell lymphoma, Leg type","['primary cutaneous diffuse large B-cell lymphoma, Leg type', 'PCDLBCL,LT']",,,178544,C1709656,,C45194,1000490,,,,,
mondo:0006412,sinus histiocytosis with massive lymphadenopathy,"['RDD', 'Rosaï-Dorfman-Destombes disease', 'sinus histiocytosis with massive lymphadenopathy', 'Destombes-Rosaï-Dorfman disease', 'Rosai-Dorfman disease', 'SHML', 'RosaC/-Dorfman-Destombes disease', 'Destombes-RosaC/-Dorfman disease']",,,158014,,,C36075,1000528,D015618,277.89,,10063397,
mondo:0006414,skin sarcoma,"['sarcoma of skin', 'sarcoma of the skin', 'sarcoma of zone of skin', 'skin sarcoma', 'cutaneous sarcoma', 'zone of skin sarcoma']",2687,,,C0856900,,C5585,1000531,,,,,
mondo:0006416,small intestinal Burkitt lymphoma,"['primary small intestinal Burkitt^s lymphoma', 'Burkitts lymphoma of small intestine', 'small intestine Burkitts lymphoma', 'small intestinal Burkitt lymphoma', 'small intestine Burkitt^s lymphoma', 'small intestinal Burkitt^s lymphoma', 'small intestine Burkitt lymphoma']",,,,C1335991,,C27409,1000533,,,,,
mondo:0006417,small intestinal diffuse large B-cell lymphoma,"['small intestinal diffuse large B-cell lymphoma', 'small intestine diffuse large B-cell lymphoma', 'diffuse large B-cell lymphoma of small intestine']",,,,C3272522,,C96055,1000534,,,,,
mondo:0006418,small intestinal enteropathy-associated T-cell lymphoma,"['small intestinal enteropathy-type T-cell lymphoma', 'small intestinal EATL', 'small intestine enteropathy-associated T-cell lymphoma', 'enteropathy-associated T-cell lymphoma of small intestine']",,,,C1519371,,C39610,1000535,,,,,
mondo:0006419,small intestinal intraepithelial neoplasia,"['small intestinal dysplasia', 'small intestinal intraepithelial neoplasia']",,,,C1335999,,C27462,1000536,,,,,
mondo:0006420,small intestinal mucosa-associated lymphoid tissue lymphoma,"['small bowel mucosa-associated lymphoid tissue lymphoma', 'MALToma of the small bowel', 'mucosa-associated lymphoid tissue lymphoma of the small intestine', 'small bowel MALT lymphoma', 'mucosa-associated lymphoid tissue lymphoma of small intestine', 'MALToma of small bowel', 'small bowel MALToma', 'mucosa-associated lymphoid tissue lymphoma of the small bowel', 'MALToma of small intestine', 'small intestine MALT lymphoma', 'MALT lymphoma of small intestine', 'small intestine mucosa-associated lymphoid tissue lymphoma', 'small intestine MALToma', 'small intestinal mucosa-associated lymphoid tissue lymphoma', 'MALT lymphoma of the small bowel', 'MALToma of the small intestine', 'MALT lymphoma of the small intestine', 'mucosa-associated lymphoid tissue lymphoma of small bowel', 'MALT lymphoma of small bowel']",,,,C1336004,,C5635,1000537,,,,,
mondo:0006421,small intestinal tubular adenoma,,,,,C1710112,,C43552,1000538,,,,,
mondo:0006422,small intestinal tubulovillous adenoma,,,,,C1710113,,C43553,1000539,,,,,
mondo:0006423,soft tissue chondroma,"['soft tissue chondroma', 'chondroma of soft parts', 'extraskeletal chondroma', 'extraskeletal osteochondroma']",3814,,,C1275277,,C9482,1000540,,,,,
mondo:0006424,soft tissue neoplasm,"['tumor of soft tissue', 'soft tissue tumour', 'soft tissue tumours', 'soft tissue tumors', 'tumour of soft tissue', 'SOFTTISSUE', 'tumour of the soft tissue', 'soft tissue neoplasm', 'neoplasm of soft tissue', 'tumor of the soft tissue', 'neoplasm of the soft tissue', 'soft tissue tumor']",,,,,,C3377,1000541,,,,,
mondo:0006426,spinal cord primitive neuroectodermal tumor,"['primitive neuroectodermal tumour of the spinal cord', 'primitive neuroectodermal neoplasm of spinal cord', 'primitive neuroectodermal tumor of the spinal cord', 'spinal cord primitive neuroectodermal neoplasm', 'spinal cord PNET', 'primitive neuroectodermal neoplasm of the spinal cord', 'spinal cord primitive neuroectodermal tumor', 'primitive neuroectodermal tumor of spinal cord', 'primitive neuroectodermal tumour of spinal cord']",6872,,,C1336048,,C5406,1000545,,,,,
mondo:0006427,spindle cell melanoma,"['spindle cell melanoma', 'spindle cell malignant melanoma', 'spitzoid malignant melanoma', 'malignant spindle cell melanoma', 'desmoplastic melanoma']",3162,,,C0334444,,C4237,1000546,,,,,
mondo:0006428,splenic diffuse large B-cell lymphoma,"['primary splenic diffuse large B-cell lymphoma', 'splenic diffuse large B-cell lymphoma']",,,,C2018774,,C7308,1000547,,,,,
mondo:0006429,splenic hodgkin lymphoma,"['splenic Hodgkin^s lymphoma', 'Hodgkin^s lymphoma of the spleen', 'primary splenic Hodgkin^s lymphoma', 'Hodgkin^s disease of the spleen', 'splenic Hodgkins lymphoma', 'Hodgkin^s disease of spleen', 'Hodgkin^s lymphoma of spleen', 'splenic Hodgkin^s disease']",,,,C0153791,,C7295,1000548,,,,,
mondo:0006430,splenic mantle cell lymphoma,['splenic mantle cell lymphoma'],,,,C2018777,,C7306,1000549,,,,,
mondo:0006432,stromal predominant kidney Wilms tumor,"['stromal predominant renal Wilms^ tumor', 'stromal predominant renal Wilms^ tumour', 'stromal predominant renal Wilm^s tumor', 'stromal predominant kidney adenosarcoma', 'stromal predominant renal Wilms tumour', 'stromal predominant Wilms tumour', 'stromal predominant kidney Wilms^ tumour', 'stromal predominant kidney Wilms^ tumor', 'stromal predominant nephroblastoma', 'stromal predominant renal Wilms tumor', 'stromal predominant renal adenosarcoma', 'stromal predominant renal Wilm^s tumour', 'stromal predominant Wilms tumor', 'stromal predominant kidney Wilms tumor']",5191,,,C0279610,,C9148,1000551,,,,,
mondo:0006435,submandibular gland adenocarcinoma,"['adenocarcinoma of the submandibular gland', 'submandibular gland adenocarcinoma', 'adenocarcinoma of submandibular gland']",,,,C1336521,,C5940,1000554,,,,,
mondo:0006436,submandibular gland adenoid cystic carcinoma,"['submandibular gland adenoid cystic carcinoma', 'adenoid cystic carcinoma of the submandibular gland', 'adenoid cystic carcinoma of submandibular gland']",,,,C1336522,,C5935,1000555,,,,,
mondo:0006438,synovial chondromatosis,"['Reichel^s syndrome', 'Henderson-Jones syndrome', 'synovial osteochondromatosis']",,,,C0008476,,C34467,1000557,D015838,,,,
mondo:0006442,tendon sheath fibroma,"['fibroma of the tendon sheath', 'tendon sheath fibroma', 'fibroma of tendon sheath']",,,,C1275236,,C6485,1000561,,215.9,,,
mondo:0006444,teratoma with malignant transformation,"['TMT', 'dermoid cyst with malignant transformation', 'teratoma with malignant transformation']",0081246,,,C0334523,,C4289,1000563,,,,,
mondo:0006446,testicular embryonal carcinoma,"['testis embryonal carcinoma', 'embryonal carcinoma of the testis', 'embryonal testis carcinoma', 'testicular embryonal carcinoma', 'embryonal carcinoma of testis']",5680,,,C0238448,,C6341,1000565,,,,,
mondo:0006447,testicular non-seminomatous germ cell tumor,"['non-dysgerminomatous germ cell tumour of testis', 'non-dysgerminomatous germ cell tumor of testis', 'testicular non-dysgerminomatous germ cell tumour', 'non-seminomatous germ cell tumor of testis', 'testicular non-dysgerminomatous germ cell tumor', 'testicular non-seminomatous germ cell tumor', 'non-seminomatous germ cell tumour of testis', 'testicular germ cell tumour non-seminomatous', 'testicular non seminomatous germ cell tumor', 'testicular non seminomatous germ cell tumour', 'testicular germ cell tumor non-seminomatous']",4086,,363494,CN204702,,C9313,1000570,,,,,
mondo:0006450,therapy-related myeloid neoplasm,"['therapy-related myeloid neoplasms', 'TMN', 'therapy-related myeloid neoplasm', 'acute myeloid Leukaemias and myelodysplastic syndromes, therapy-related', 'therapy-related AML and MDS', 'therapy-related acute myeloid leukemia and myelodysplastic syndrome', 'therapy-related acute myeloid leukaemia and myelodysplastic syndrome']",,,,,,C27912,1000575,,,,,
mondo:0006451,thymic carcinoma,"['thymoma type C', 'thymoma, malignant', 'thymus carcinoma', 'type C thymoma', 'thymic carcinoma (excluding well differentiated thymic carcinoma)', 'malignant thymoma', 'thymic carcinoma excluding well differentiated thymic carcinoma', 'thymic carcinoma', 'carcinoma of thymus', 'thymoma, malignant (morphologic abnormality)', 'thymoma, type C', 'thymoma, type C (morphologic abnormality)', 'THYC']",4554,,99868,CN207411,,C7569,1000576,,,,10061031,
mondo:0006452,thymic sarcomatoid carcinoma,"['Thymus sarcomatoid carcinoma', 'thymic sarcomatoid carcinoma', 'thymic carcinosarcoma', 'sarcomatoid carcinoma of Thymus', 'sarcomatoid carcinoma of the Thymus', 'thymus sarcomatoid carcinoma', 'thymic spindle cell carcinoma']",8138,,,C1335924,,C6463,1000577,,,,,
mondo:0006455,thymic undifferentiated carcinoma,['thymic undifferentiated carcinoma'],,,,C1336865,,C35718,1000580,,,,,
mondo:0006456,thymoma,"['THYM', 'primary thymic epithelial tumor', 'thymoma', 'primary thymic epithelial tumour', 'thymoma (disease)', 'primary thymic epithelial neoplasm']",3275,,99867,C0040100,,C3411,1000581,D013945,239.89,D15.0,10043670,0100522
mondo:0006458,thymoma type B3,"['epithelial thymoma', 'atypical thymoma', 'epithelial malignant thymoma', 'well-differentiated thymic carcinoma', 'malignant thymoma type B3', 'thymoma type B3', 'squamoid thymoma', 'well differentiated thymic carcinoma', 'thymoma, epithelial']",7926,,,C0279705,,C7997,1000583,,,,,
mondo:0006459,thymoma type B1,"['predominantly cortical thymoma', 'lymphocyte-rich thymoma', 'organoid thymoma', 'lymphocyte-predominant thymoma', 'thymoma type B1', 'thymoma, organoid']",6917,,,C1266094,,C6887,1000584,,,,,
mondo:0006460,thyroglossal duct cyst,['thyroglossal tract cyst'],,,489,,,,1000585,D013955,759.2,,,
mondo:0006462,thyroid gland diffuse large B-cell lymphoma,"['diffuse large B-cell lymphoma of the thyroid gland', 'diffuse large B-cell lymphoma of thyroid gland', 'thyroid diffuse large B-cell lymphoma', 'primary thyroid gland diffuse large B-cell lymphoma', 'diffuse large B-cell lymphoma of the thyroid', 'thyroid gland diffuse large B-cell lymphoma', 'diffuse large B-cell lymphoma of thyroid']",,,,C1336749,,C6046,1000587,,,,,
mondo:0006463,thyroid gland mucoepidermoid carcinoma,"['thyroid gland mucoepidermoid carcinoma', 'mucoepidermoid thyroid carcinoma', 'mucoepidermoid thyroid gland carcinoma']",4687,,,C1513721,,C38762,1000590,,,,,
mondo:0006464,thyroid gland mucosa-associated lymphoid tissue lymphoma,"['thyroid mucosa-associated lymphoid tissue lymphoma', 'thyroid MALT lymphoma']",,,,C1336754,,C7601,1000591,,,,,
mondo:0006465,thyroid gland oncocytic follicular carcinoma,"['oncocytic carcinoma of the thyroid', 'thyroid gland Hurthle cell carcinoma', 'Hurthle cell carcinoma of thyroid', 'Hurthle cell carcinoma of the thyroid', 'Hurthle cell carcinoma of thyroid gland', 'Hurthle cell carcinoma of the thyroid gland', 'thyroid Hurthle cell carcinoma', 'Hurthle cell thyroid gland carcinoma', 'oncocytic carcinoma of thyroid', 'thyroid oncocytic carcinoma']",,,,,,C4946,1000592,,,,,
mondo:0006466,thyroid gland spindle cell tumor with thymus-like differentiation,"['spindle epithelial tumour with thymus-like differentiation tumour', 'spindle epithelial tumor with thymus-like differentiation tumor', 'settle tumour', 'settle tumor', 'settle']",0050923,,,C1266099,,C46105,1000593,,,,,
mondo:0006467,thyroid gland squamous cell carcinoma,"['squamous cell thyroid gland carcinoma', 'thyroid gland squamous cell carcinoma']",,,,C1710177,,C46008,1000594,,,,,
mondo:0006468,thyroid gland undifferentiated (anaplastic) carcinoma,"['thyroid gland carcinosarcoma', 'thyroid gland undifferentiated carcinoma', 'undifferentiated carcinoma of the thyroid gland', 'anaplastic carcinoma of the thyroid', 'THAP', 'thyroid cancer, anaplastic', 'undifferentiated thyroid tumor', 'undifferentiated carcinoma of the thyroid', 'undifferentiated thyroid carcinoma', 'anaplastic carcinoma of thyroid', 'undifferentiated carcinoma of thyroid gland', 'undifferentiated carcinoma of thyroid', 'anaplastic thyroid carcinoma', 'undifferentiated (anaplastic) thyroid gland carcinoma', 'undifferentiated thyroid tumour', 'pleomorphic thyroid gland carcinoma', 'anaplastic thyroid cancer', 'metaplastic thyroid gland carcinoma', 'undifferentiated (anaplastic) thyroid gland cancer', 'anaplastic carcinoma of the thyroid gland', 'thyroid gland undifferentiated (anaplastic) carcinoma', 'anaplastic carcinoma of thyroid gland', 'undifferentiated thyroid gland carcinoma', 'Dedifferentiated thyroid gland carcinoma', 'thyroid carcinoma, anaplastic', 'anaplastic thyroid gland carcinoma', 'sarcomatoid thyroid gland carcinoma']",0080522,,142,C0238461,,C3878,1000595,D065646,,,10002240,0011779
mondo:0006469,tibial adamantinoma,"['tibial adamantinoma morphology', 'tibial adamantinoma', 'adamantinoma of tibia', 'tibia long bone adamantinoma', 'tibia adamantinoma']",6322,,,C1273017,,C8461,1000596,,,,,
mondo:0006470,tonsillar squamous cell carcinoma,"['palatine tonsil squamous cell carcinoma', 'scc of the tonsil', 'squamous cell carcinoma of the tonsil', 'squamous cell carcinoma of tonsil', 'scc of tonsil', 'tonsil scc', 'tonsillar scc']",,,,C0280317,,C8183,1000597,,,,,
mondo:0006471,tracheal adenoid cystic carcinoma,"['tracheal adenoid cystic carcinoma', 'trachea adenoid cystic carcinoma', 'adenoid cystic carcinoma of the trachea', 'adenoid cystic carcinoma of trachea']",4875,,,C0345945,,C6051,1000598,,,,,
mondo:0006474,transitional cell carcinoma,"['transitional cell tumor', 'transitional cell carcinoma', 'carcinoma of transitional epithelial cell', 'urothelial cell carcinoma', 'transitional cell neoplasm', 'transitional cell tumour', 'transitional carcinoma', 'carcinoma, urothelial, malignant', 'carcinoma of urothelial cell']",2671,,,C0334265,,C6783,1000601,D002295,,,,
mondo:0006476,undifferentiated gallbladder carcinoma,"['gallbladder undifferentiated carcinoma', 'anaplastic gallbladder carcinoma', 'undifferentiated carcinoma of gallbladder', 'undifferentiated gallbladder cancer', 'anaplastic carcinoma of the gallbladder', 'anaplastic carcinoma of gallbladder', 'undifferentiated gallbladder carcinoma', 'gall bladder undifferentiated carcinoma', 'undifferentiated carcinoma of the gallbladder']",,,,C0279653,,C9167,1000604,,,,,
mondo:0006477,undifferentiated ovarian carcinoma,"['undifferentiated ovarian cancer', 'undifferentiated carcinoma of the ovary', 'undifferentiated carcinoma of ovary', 'ovary undifferentiated carcinoma', 'anaplastic carcinoma of ovary', 'anaplastic ovarian carcinoma', 'undifferentiated ovarian carcinoma', 'ovarian undifferentiated carcinoma', 'anaplastic carcinoma of the ovary']",,,,C0346167,,C4509,1000605,,,,,
mondo:0006478,undifferentiated pancreatic carcinoma,"['pancreas undifferentiated carcinoma', 'pleomorphic large cell pancreatic carcinoma', 'undifferentiated carcinoma of the pancreas', 'sarcomatoid pancreatic carcinoma', 'undifferentiated carcinoma of pancreas', 'spindle cell pancreatic carcinoma', 'undifferentiated pancreatic carcinoma', 'UCP', 'undifferentiated (anaplastic) pancreatic carcinoma', 'pancreatic carcinosarcoma']",,,,C1336861,,C5722,1000606,,,,,
mondo:0006479,undifferentiated pancreatic carcinoma with osteoclast-like giant cells,"['pancreatic osteoclastic giant cell tumour', 'osteoclastic giant cell tumor of pancreas', 'undifferentiated carcinoma of pancreas with osteoclast-like giant cells', 'osteoclast-like giant cell neoplasm of the pancreas', 'pancreatic osteoclastic giant cell tumor', 'undifferentiated pancreatic carcinoma with osteoclast-like giant cells', 'osteoclast-like giant cell neoplasm of pancreas', 'osteoclastic giant cell tumour of pancreas', 'pancreatic undifferentiated carcinoma with osteoclast-like giant cells', 'pancreatic osteoclast-like giant cell carcinoma', 'OGCT of pancreas']",7718,,424080,CN237530,,C5723,1000607,,,,,
mondo:0006480,"undifferentiated pleomorphic sarcoma, inflammatory variant","['inflammatory MFH', 'Xanthosarcoma', 'malignant xanthogranuloma', 'undifferentiated pleomorphic sarcoma, inflammatory variant', 'inflammatory malignant fibrous histiocytoma']",6192,,,C1334180,,C6497,1000608,,,,,
mondo:0006481,ureter carcinoma,"['ureter cancer', 'carcinoma of ureter', 'carcinoma of the ureter', 'ureter carcinoma', 'ureteral carcinoma']",4939,,,C0600079,,C8993,1000609,,,,,
mondo:0006482,ureter small cell carcinoma,"['small cell carcinoma of the ureter', 'small cell carcinoma of ureter', 'ureteral small cell carcinoma', 'ureter small cell carcinoma']",6886,,,C1336878,,C6176,1000610,,,,,
mondo:0006483,urothelial dysplasia,"['transitional cell dysplasia of the urinary tract', 'urothelial dysplasia']",,,,C1275859,,C39856,1000611,,,,,
mondo:0006484,usual ductal breast hyperplasia,"['ordinary intraductal breast hyperplasia', 'UDH', 'ductal breast hyperplasia of usual type']",,,,C3532429,,C27941,1000612,,611.89,,,
mondo:0006485,uterine carcinosarcoma,"['uterine malignant mixed mesodermal (Mullerian) tumour', 'uterus carcinosarcoma', 'uterine carcinosarcoma/uterine malignant mixed mullerian tumor', 'uterine carcinosarcoma/uterine malignant mixed mullerian tumour', 'malignant mixed mesodermal (Müllerian) tumor of the uterus', 'carcinosarcoma of the uterus', 'malignant mixed mesodermal (Mullerian) tumor of the uterus', 'malignant mixed mesodermal (Mullerian) tumour of the uterus', 'mixed mullerian sarcoma of uterus', 'uterine malignant mixed mesodermal (Mullerian) tumor', 'uterine malignant mixed mesodermal (Müllerian) tumour', 'uterine malignant mixed mesodermal (Müllerian) tumor', 'uterine carcinosarcoma', 'malignant mixed mesodermal (Müllerian) tumour of the uterus']",6171,,,C0280630,,C42700,1000613,D012192,,,,
mondo:0006486,uveal melanoma,"['melanoma of the uvea', 'melanoma of uvea', 'choroidal melanoma', 'uveal melanoma', 'melanoma, uveal, malignant', 'iris melanoma', 'uvea melanoma (disease)', 'intraocular melanoma']",6039,155720,39044,C0220633,,C7712,1000616,C536494,,,10061252,
mondo:0006487,vaginal adenoid cystic carcinoma,"['vaginal adenoid cystic cancer', 'vaginal adenoid cystic carcinoma']",,,,C1519912,,C40261,1000617,,,,,
mondo:0006488,vaginal carcinosarcoma,"['vaginal malignant mixed mesodermal (Müllerian) tumor', 'vaginal carcinosarcoma', 'vaginal malignant mixed mesodermal (Mullerian) tumour', 'vaginal mixed epithelial and mesenchymal tumour', 'vaginal mixed epithelial and mesenchymal tumor', 'vaginal malignant mixed mesodermal (Müllerian) tumour', 'vaginal malignant mixed mesodermal (Mullerian) tumor', 'malignant vaginal mixed epithelial and mesenchymal tumor', 'malignant vaginal mixed epithelial and mesenchymal tumour', 'vaginal malignant mixed Mullerian tumor', 'vaginal malignant mixed Mullerian tumour']",136,,,C1519918,,C40278,1000618,,,,,
mondo:0006489,vaginal melanoma,"['vagina melanoma (disease)', 'melanoma of vagina', 'mucosal melanoma of the vulva/vagina', 'melanoma of the vagina', 'vaginal melanoma']",,,,C2004576,,C27394,1000619,,,,,
mondo:0006490,vaginal squamous cell carcinoma,"['vaginal epidermoid cell carcinoma', 'epidermoid carcinoma of the vagina', 'epidermoid carcinoma of vagina', 'vaginal epidermoid carcinoma', 'carcinoma of vagina squamous cell', 'vagina epidermoid carcinoma', 'epidermoid cell carcinoma of the vagina', 'epidermoid cell carcinoma of vagina', 'vagina epidermoid cell carcinoma', 'vagina squamous cell carcinoma', 'squamous cell carcinoma of vagina', 'squamous cell carcinoma of the vulva/vagina', 'squamous cell carcinoma of the vagina', 'vaginal squamous cell cancer, NOS', 'vaginal squamous cell cancer', 'vaginal squamous cell carcinoma']",,,,C0238518,,C7736,1000620,,,,,
mondo:0006491,vulvar lichen sclerosus,"['lichen sclerosus et atrophicus of mammalian vulva', 'mammalian vulva lichen sclerosus et atrophicus', 'vulvar lichen sclerosus']",,,,C0022783,,C27723,1000623,D007724,,,,
mondo:0006493,Warthin tumor,"['Warthin^s tumor', 'papillary cystadenoma lymphomatosum (formerly)', 'Warthin^s tumour', 'papillary cystadenoma lymphomatosum', 'adenolymphoma', 'Warthin tumor']",,,,C0001429,,C2854,1000625,D000235,,,,
mondo:0006496,palsy,"['Plegias', 'Plegia']",,,,,,,1000631,D010243,,G80-G83,,
mondo:0006497,cerebral palsy,['infantile cerebral palsy'],1969,,,C0007789,,C34460,1000632,D002547,343.9,G80,,0100021
mondo:0006498,adenomatous colon polyp,"['colonic adenomatous polyp', 'adenomatous polyp of colon', 'adenomatous polyp of the colon', 'colon adenomatous polyp']",,,,,,C96479,1000633,,,,,0005227
mondo:0006499,hamartoma,"['hamartoma (disease)', 'hamartoma']",,,,C0018552,,C3075,1000634,D006222,759.6,,,0010566
mondo:0006500,hemangioma,"['hemangioma, benign', 'benign hemangioma', 'benign angioma', 'hemangioma', 'angioma']",255,,,C0018916,,C3085,1000635,D006391,228.09,,,0001028
mondo:0006502,acute respiratory distress syndrome,"['increased-permeability pulmonary edema', 'shock lung', 'non-cardiogenic pulmonary oedema', 'ARDS', 'non-cardiogenic pulmonary edema', 'Stiff lung', 'acute respiratory distress syndrome', 'ALI', 'increased-permeability pulmonary oedema', 'acute lung injury']",,,,,,C3353,1000637,,,J80,10001052,
mondo:0006504,acquired metabolic disease,['acquired metabolic disease'],0060158,,,,,,1000639,,,,,
mondo:0006505,basal ganglia cerebrovascular disorder,"['cerebrovascular disorder of collection of basal ganglia', 'collection of basal ganglia cerebrovascular disorder']",10991,,,C0751739,,,1000640,D020144,,,,
mondo:0006506,congenital nonspherocytic hemolytic anemia,"['hereditary nonspherocytic hemolytic anaemia', 'hereditary nonspherocytic hemolytic anemia', 'HNSHA']",2861,,,C0002882,,,1000641,D000746,282.3,,,
mondo:0006507,hereditary hemochromatosis,"['diabetes bronze', 'haemochromatosis', 'iron storage disorder', 'hemochromatosis, hereditary', 'hemochromatosis']",2352,,,,,C84481,1000642,D006432,,E83.110,,
mondo:0006509,papillary carcinoma,"['papillary carcinoma NOS (morphologic abnormality)', 'papillary carcinoma', 'papillary carcinoma (morphologic abnormality)']",3113,,,C0007133,,C2927,1000646,D002291,,,,
mondo:0006510,renal tubular transport disease,"['kidney tubular transport, inborn error', 'inborn renal tubular transport disorder', 'renal absorption disease', 'renal tubular transport errors', 'renal tubular transport, inborn error', 'disorder of renal absorption', 'kidney tubular transport, inborn errors']",447,,,C0035091,,,1000647,D015499,,,,
mondo:0006512,estrogen-receptor positive breast cancer,['oestrogen receptor positive breast cancer'],0060075,,,,,,1000649,,,,,
mondo:0006513,estrogen-receptor negative breast cancer,,0060076,,,,,,1000650,,,,,
mondo:0006514,recalcitrant atopic dermatitis,,,,,,,,1000651,,,,,
mondo:0006515,acute pancreatitis,"['pancreatitis, acute', 'acute pancreatitis (disorder) [ambiguous]']",2913,,,C0267941,,C95437,1000652,,577.0,,,0001735
mondo:0006517,childhood malignant neoplasm,"['malignant pediatric tumor', 'malignant childhood tumor', 'childhood malignant neoplasm', 'malignant neoplasm', 'malignant paediatric tumour', 'pediatric cancer', 'malignant childhood tumour', 'malignant childhood neoplasm', 'malignant pediatric neoplasm', 'paediatric cancer', 'malignant paediatric neoplasm', 'childhood cancer', 'childhood neoplasm, malignant']",,,,C0278704,,C4005,1000654,,,,,
mondo:0006518,sporadic Creutzfeld Jacob disease,,,,,,,,1000656,,,,,
mondo:0006519,rectal cancer,"['malignant neoplasm of the rectum', 'malignant tumor of the rectum', 'malignant tumour of rectum', 'cancer of rectum', 'malignant rectum tumor', 'malignant tumor of rectum', 'malignant rectum neoplasm', 'malignant neoplasm of rectum', 'malignant rectum tumour', 'malignant tumour of the rectum', 'carcinoma of the rectum', 'malignant rectal tumour', 'malignant rectal neoplasm', 'rectal cancer', 'rectum cancer', 'malignant rectal tumor', 'carcinoma of rectum']",1993,,,,,C7418,1000657,,154.1,,,
mondo:0006520,Achenbach syndrome,"['paroxysmal hematoma of the finger', 'Achenbach syndrome']",6687,,,,,C35467,1000661,,,,,
mondo:0006521,acneiform dermatitis,['Rash acneiform'],4399,,,C0234894,,C35277,1000662,,,,,
mondo:0006522,acquired keratosis,"['keratoderma, acquired', 'acquired keratoderma', 'acquired hyperkeratosis', 'keratoderma - acquired', 'acquired keratosis']",13072,,,,,C34746,1000663,,701.1,,,
mondo:0006523,acrodermatitis,,2722,,,C0001197,,C84532,1000664,D000169,686.8,,,
mondo:0006524,acrodermatitis chronica atrophicans,"['Herxheimer disease', 'primary diffuse atrophy']",0060344,,,C0263421,,,1000665,,701.8,L90.4,,
mondo:0006525,allergic contact dermatitis,"['allergic form of contact dermatitis', 'allergic contact dermatitis']",3042,,,C0162820,,C26998,1000668,D017449,692.9,L23,,
mondo:0006526,allergic urticaria,"['allergic form of urticaria (disease)', 'allergic form of urticaria']",10612,,,C0149526,,,1000669,,708.0,L50.0,,
mondo:0006527,anhidrosis,"['absence of sweating', 'adiaphoresis']",11156,,,,,,1000670,D007007,705.0,L74.4,,
mondo:0006528,bacterial exanthem,,0050487,,,,,,1000671,,,,,
mondo:0006530,cholesteatoma,"['congenital cholesteatoma (type)', 'cholesteatoma (disease)', 'secondary acquired cholesteatoma (type)', 'primary acquired cholesteatoma (type)', 'cholesteatoma']",869,,,C0008373,,C2944,1000675,D002781,385.30,,,0009797
mondo:0006531,cholesteatoma of attic,,10963,,,C0155489,,,1000676,,385.31,,,
mondo:0006532,cholesteatoma of external ear,"['external ear cholesteatoma (disease)', 'external canal cholesteatoma']",9462,,,C0155398,,,1000677,,380.21,H60.4,,
mondo:0006533,cholesteatoma of middle ear,"['middle ear cholesteatoma', 'cholesteatoma of middle ear', 'unspecified cholesteatoma (morphologic abnormality)', 'cholesteatoma of the middle ear', 'cholesteatoma of middle ear and/or mastoid', 'middle ear cholesteatoma (disease)', 'cholesteatoma of middle ear and mastoid', 'Epidermosis of ear', 'Epidermosis of middle ear']",10964,,,C0155490,,C3654,1000678,D018424,385.33,H71,,
mondo:0006534,cholinergic urticaria,,14443,,,C0152230,,,1000679,,708.5,L50.5,,
mondo:0006536,congenital generalized lipodystrophy,"['hereditary generalised lipodystrophy', 'familial generalised lipodystrophy', 'familial generalized lipodystrophy', 'congenital generalized lipodystrophy (disease)', 'lipodystrophy, congenital generalised', 'congenital generalised lipodystrophy (disease)', 'lipodystrophy, congenital generalized', 'congenital generalized lipodystrophy', 'hereditary generalized lipodystrophy']",0050585,,,,,,1000681,,,,,0009059
mondo:0006537,conjunctival pigmentation,,12304,,,C0155163,,,1000682,,372.55,,,
mondo:0006539,diffuse lipomatosis,['diffuse lipomatosis'],3923,,,C1333298,,C6504,1000687,,,,,
mondo:0006540,dyshidrosis,"['vesicular eczema of hands and/or feet', 'dyshidrosis', 'DYSHYDROTIC eczema', 'cheiropompholyx', 'pompholyx']",9230,,,C0032633,,,1000688,D011146,705.81,,,
mondo:0006541,epidermolysis bullosa,"['EB', 'acantholysis bullosa', 'epidermolysis bullosa']",2730,,,,,C67383,1000690,D004820,757.39,Q81,,
mondo:0006543,epidermolysis bullosa dystrophica,"['epidermolysis bullosa, dermolytic', 'DEB', 'epidermolysis bullosa dystrophica', 'dermolytic epidermolysis bullosa']",4959,,303,,"['0.709', '-0.2441', '-0.2773', '-0.1598', '-0.00948', '-0.6504', '-0.6216', '0.3901', '-0.3357', '-0.688', '0.3037', '-0.2683', '-0.8433', '0.4924', '-0.62', '0.05618', '0.2382', '-1.062', '-0.326', '-0.996', '-0.0931', '-0.372', '0.427', '0.585', '0.5396', '0.1487', '-1.115', '0.8', '-0.5273', '-0.8716', '0.1383', '-0.06934', '-0.4355', '-0.05957', '0.02798', '0.1229', '-1.15', '0.1721', '1.308', '-0.5874', '-0.05927', '-0.747', '0.2313', '0.04922', '-0.009705', '-0.2805', '-0.2146', '0.04538', '0.7676', '-0.09625', '-0.616', '-0.681', '0.4866', '-0.08203', '-0.02173', '-0.5225', '-0.078', '1.274', '-0.8467', '-0.268', '-0.02939', '0.412', '0.1377', '0.3997', '0.991', '0.7905', '0.3257', '0.2776', '-0.6367', '0.196', '-0.2556', '-0.132', '-0.5684', '-0.1389', '-0.05124', '-0.01139', '-0.11115', '0.2043', '-0.002773', '-0.3486', '-1.02', '0.04102', '-0.302', '-0.0949', '0.1647', '0.3184', '-0.99', '0.726', '0.993', '0.3486', '-0.6187', '0.5806', '0.0168', '0.6216', '-0.0404', '0.899', '0.1456', '-0.72', '0.7373', '0.1644']",C84691,1000692,D016108,757.39,,,
mondo:0006544,erythema infectiosum,['fifth disease'],8743,,,C0085273,,C84695,1000693,D016731,057.0,,,
mondo:0006545,erythema multiforme,"['Herpes iris, erythema multiforme type', 'EM', 'erythema polymorphe, erythema multiforme type', 'erythema multiforme bullosum', 'febrile mucocutaneous syndrome', 'Dermatostomatitis, erythema multiforme type']",0050185,,,C0014742,,C3024,1000694,D004892,695.10,L51,,
mondo:0006546,erythematosquamous dermatosis,"['Other erythematosquamous dermatosis', 'erythematosquamous dermatosis']",9097,,,C0014747,,C34591,1000695,,690.8,,,
mondo:0006547,exanthem,"['skin eruption', 'exanthem (disease)', 'cutaneous eruption', 'skin Rash', 'exanthema', 'Rash', 'exanthem']",0050486,,,,,C39594,1000697,D005076,782.1,,,0000988
mondo:0006548,facial dermatosis,,3134,,,C0015456,,,1000698,D005148,,,,
mondo:0006549,fibroepithelial polyp of the anus,"['anus skin tag', 'fibrous polyp of anus', 'anal tag', 'fibrous polyp of the anus', 'fibroepithelial polyp of anus', 'anal fibrous polyp', 'anal fibroepithelial polyp']",8170,,,,,C4435,1000699,,,,,
mondo:0006550,fibroepithelial polyp of urethra,"['fibroepithelial polyp of urethra', 'urethra skin tag', 'urethra fibroepithelial polyp', 'urethral fibroepithelial polyp', 'fibroepithelial polyp of the urethra']",8108,,,C1336884,,C6170,1000700,,,,,
mondo:0006551,alopecia mucinosa,"['hair follicle cutaneous focal mucinosis', 'alopecia mucinosis', 'follicular mucinosis', 'alopecia Mucinosa', 'cutaneous focal mucinosis of hair follicle', 'alopecia mucinosa']",9905,,,C0002173,,C82859,1000701,D000507,704.09,L65.2,,
mondo:0006552,folliculitis,"['dermatitis of hair follicle', 'hair follicle dermatitis']",4409,,,,,C94408,1000702,D005499,704.8,,,
mondo:0006553,Fox-Fordyce disease,"['Fox-Fordyce syndrome', 'miliaria, apocrine', 'Fox-Fordyce disease', 'Fox Fordyce disease', 'apocrine miliaria']",1381,,,C0016632,,C84716,1000703,D005588,705.82,L75.2,,
mondo:0006554,granuloma annulare,"['granuloma annulare', 'Granulome annulare']",3777,,,C0085074,,C3470,1000704,D016460,709.8,L92.0,,
mondo:0006555,granulomatous dermatitis,,4397,,,C0743086,,C3505,1000705,,,,,
mondo:0006556,hand dermatosis,,3158,,,C0018567,,,1000706,D006229,,,,
mondo:0006557,hemangioma of subcutaneous tissue,"['superficial fascia hemangioma', 'subcutaneous tissue angioma', 'hemangioma of the subcutaneous tissue', 'hemangioma of superficial fascia', 'subcutaneous hemangioma', 'subcutaneous tissue hemangioma', 'angioma of the subcutaneous tissue', 'subcutaneous angioma', 'angioma of subcutaneous tissue', 'hemangioma of subcutaneous tissue', 'subcutaneous haemangioma']",13081,,,C0685200,,C8540,1000707,,,,,
mondo:0006558,pemphigoid gestationis,"['Herpes gestationis', 'gestational pemphigoid', 'Herpes gestationis NOS (disorder)', 'gestational herpes', 'pemphigus gestationis', 'pemphigoid gestationis', 'Herpes gestationis (disorder)', 'Herpes gestationis unspecified (disorder)']",14482,,63275,C0019343,,C85003,1000709,D006559,646.80,,10019939,
mondo:0006559,hidradenitis suppurativa,"['fox den disease', 'pyoderma fistulans significa', 'hidradenitis suppurativa', 'acne inversa', 'verneuil disease', 'acne inversa, familial', 'ectopic acne']",2280,,387,C0162836,,,1000710,D017497,,L73.2,,
mondo:0006561,eyelid hypopigmentation,,11668,,,C0155212,,,1000713,,374.53,,,
mondo:0006563,inverted follicular keratosis,"['inverted folicular keratosis', 'inverted follicular keratosis']",6945,,,C0334019,,C9007,1000717,,264.8,,,
mondo:0006564,irritant dermatitis,"['primary irritant dermatitis', 'irritant contact dermatitis']",2772,,,C0162823,,C27151,1000718,D017453,692.9,,,
mondo:0006565,juvenile dermatitis herpetiformis,,8507,,,C0152092,,,1000719,,694.2,,,
mondo:0006566,keratosis,['keratoderma'],161,,,C0022593,,C34745,1000720,D007642,,,,
mondo:0006567,kernicterus due to isoimmunization,"['kernicterus - due to isoimm.', 'kernicterus related to isoimmunization', 'kernicterus due to isoimmunization of foetus or newborn', 'kernicterus due to isoimmunization of fetus or newborn']",12043,,,C0270204,,C101270,1000721,,773.4,P57.0,,
mondo:0006569,leg dermatosis,,3142,,,C0023219,,,1000723,D007868,,,,
mondo:0006570,lichen disease,,8574,,,C0023643,,,1000724,,697.9,,,
mondo:0006571,lichen nitidus,['Pinkus^ disease'],8573,,,C0162849,,,1000725,D017513,697.1,L44.1,,
mondo:0006572,lichen planus,"['lichen, ruber planus', 'lichen ruber planus']",9201,,,C0023646,,C3189,1000726,D008010,697.0,L43,,
mondo:0006573,lipodystrophy,"['lipodystrophy', 'lipodsystrophic syndromes', 'lipodsystrophic syndrome', 'lipodystrophy (disease)']",811,,,C0023787,,C97093,1000727,D008060,272.6,,,0009125
mondo:0006574,lipomatosis,"['Madelung disease', 'Madelung^s disease', 'lipomatosis', 'Launois-Bensaude syndrome']",3153,,,C0023801,,C3193,1000728,D008068,272.8,,,
mondo:0006576,Ludwig^s angina,"['cellulitis of floor of mouth', 'mouth floor cellulitis (disease)', 'Ludwig angina']",4558,,,C3247204,,,1000730,D008158,528.3,,,
mondo:0006577,maxillary sinus cholesteatoma,['maxillary sinus cholesteatoma (disease)'],867,,,C1334644,,C35868,1000731,,,,,
mondo:0006578,mediastinal lipomatosis,['mediastinal lipomatosis'],3926,,,C1334662,,C27488,1000732,,,,,
mondo:0006579,melanoacanthoma,,11684,,,C1321683,,C27548,1000733,,,,,
mondo:0006580,miliaria,"['prickly heat', 'heat rash']",1382,,,C0026113,,C34820,1000734,D008883,,,,
mondo:0006581,miliaria rubra,"['prickly heat - miliaria', 'sudamina', 'miliaria crystallina']",11153,,,C3241961,,,1000735,,705.1,,,
mondo:0006582,mongolian spot,"['Mongolian macula', 'congenital dermal melanocytosis', 'blue sacral spot']",4702,,,C0265985,,C3945,1000736,D049328,,,,
mondo:0006583,necrobiosis lipoidica,"['necrobiosis lipoidica diabeticorum (formerly)', 'necrobiosis lipoidica']",3486,,542592,C0027538,,C34840,1000738,D009335,,,,
mondo:0006585,neurodermatitis,['lichen simplex Chronicus'],3309,,,C0149922,,C111963,1000740,D009450,,,,
mondo:0006586,neurotic excoriation,"['factitious skin disease', 'dermatitis factitia [artefacta]', 'dermatitis factitia', 'dermatitis artefacta', 'dermatitis ficta']",9165,,,C1274184,,,1000741,,698.4,,,
mondo:0006589,occupational dermatitis,"['occupational allergic contact dermatitis', 'occupational dermatitis', 'occupational eczema (disorder) [ambiguous]', 'occupational eczema']",4404,,,C0028796,,C34859,1000744,D009783,692.9,,,
mondo:0006590,palmoplantar keratosis,"['keratosis palmaris et plantaris', 'palmoplantar keratoderma', 'keratoderma, palmoplantar']",3390,,,,,C34748,1000745,,757.39,,,
mondo:0006591,panniculitis,"['Subcutaneous adipose tissue', 'subcutaneous adipose tissue inflammation', 'Subcutaneous tissue', 'subcutis']",1526,,,C0030326,,C33645,1000746,D015434,729.39,,,
mondo:0006592,parapsoriasis,"['digitate dermatosis', 'parapsoriasis en plaque']",9088,,,C0030491,,C3312,1000747,D010267,696.2,L41,,
mondo:0006593,pelvic lipomatosis,"['pelvic lipomatosis (morphologic abnormality)', 'pelvic lipomatosis', 'Excess of mature unencapsulated fatty tissue in the pelvis']",3927,,,C0406608,,C27486,1000748,C535549,,,,
mondo:0006594,pemphigus,,9182,,,C0030807,,C34909,1000749,D010392,694.4,L10,,
mondo:0006595,perinatal jaundice due to hepatocellular damage,,11452,,,C0158976,,,1000750,,774.4,,,
mondo:0006596,photoallergic dermatitis,"['photoallergic contact dermatitis', 'photoallergic eczema']",3818,,,C0162824,,,1000751,D017454,692.72,,,
mondo:0006597,photosensitivity disease,"['disorder, photosensitivity', 'disorders, photosensitivity', 'photodermatitides', 'photodermatitis', 'photosensitivity disorder', 'photosensitization']",3159,,,C0031762,,,1000752,D010787,,,,
mondo:0006598,phototoxic dermatitis,"['Photodermatitis', 'Photosensitisation reaction', 'photosensitive dermatitis', 'photosensitiveness', 'photosensitivity reaction']",4407,,,C0162830,,C4816,1000753,D017484,,,,
mondo:0006599,physical urticaria,,0060220,,,,,,1000754,,,,,
mondo:0006601,pityriasis rosea,"['Pityriasis circinata', 'Pityriasis rosea']",8892,,,C0032026,,C26855,1000756,D017515,696.3,L42,,
mondo:0006602,porokeratosis,"['porokeratosis (disease)', 'porokeratosis']",3805,,79358,C0162839,,C85019,1000757,D017499,757.39,,10036175,0200044
mondo:0006603,reactive cutaneous fibrous lesion,,2053,,,C1335666,,C27549,1000759,,,,,
mondo:0006604,rosacea,"['acne rosacea', 'acne roscea', 'acne, erythematosa']",8881,,,C0035854,,C97136,1000760,D012393,695.3,L71,,
mondo:0006605,scalp dermatosis,['dermatosis of scalp'],3136,,,C0036271,,,1000761,D012536,,,,
mondo:0006606,scleredema adultorum,"['scleredemas', 'Buschke scleredema Diabeticorum', 'Diabeticorums, scleredema', 'scleredema Diabeticorums', 'scleredema Diabeticorum of Buschke', 'scleredema adultorum of Buschke', 'Buschke^s scleredema', 'scleredema adultorum', 'Buschke scleredema adultorum', 'Buschkes scleredema', 'scleredema Diabeticorum', 'scleredema, Buschke^s', 'Buschke scleredema', 'Diabeticorum, scleredema', 'scleredema']",3140,,352763,C0036413,,C85057,1000762,D012592,,,,
mondo:0006607,sebaceous gland disorder,"['sebaceous gland disease or disorder', 'disease of sebaceous gland', 'sebaceous gland disease', 'disorder of sebaceous gland']",9098,,,C0036502,,,1000763,D012625,706.1,,,
mondo:0006608,seborrheic dermatitis,"['seborrhea', 'cradle Cap', 'seborrheic dermatitis (disease)', 'Seborrhoeic dermatitis', 'seborrheic eczema', 'skin seborrheic', 'Seborrhoeic eczema', 'seborrheic dermatitis']",8741,,,C0036508,,C111888,1000764,D012628,706.3,,,0001051
mondo:0006609,seborrheic infantile dermatitis,"['infantile seborrheic dermatitis', 'scalp seborrheic dermatitis (disease)', 'infantile seborrhoeic dermatitis', 'seborrhea sicca', 'generalized seborrheic dermatitis of infants', 'generalised seborrheic dermatitis of infants', 'pityriasis capitis', 'cradle cap', 'Seborrhoeic eczema of scalp', 'Seborrhoeic dermatitis of scalp', 'Seborrhoea capitis', 'seborrhea capitis', 'complement 5 dysfunction']",8941,,,,,,1000765,,690.11,,,
mondo:0006610,skin atrophy,"['atrophic condition of skin', 'atrophy of skin', 'atrophy - skin', 'atrophoderma', 'atrophic skin']",2733,,,C0151514,,C35163,1000766,,701.8,,,
mondo:0006611,skin sarcoidosis,"['zone of skin sarcoidosis', 'cutaneous sarcoid', 'cutaneous sarcoidosis', 'sarcoidosis of zone of skin']",13402,,,C0036203,,C34996,1000767,,,D86.3,,
mondo:0006612,steroid lipomatosis,['steroid lipomatosis'],3925,,,C1336506,,C27487,1000769,,,,,
mondo:0006613,stromal corneal pigmentation,['stromal corneal pigmentations'],12311,,,C0155105,,,1000770,,371.12,,,
mondo:0006614,subcorneal pustular dermatosis,"['subcorneal pustular dermatosis', 'Sneddon-Wilkinson disease or syndrome', 'subcorneal pustular dermatitis', 'pustulosis subcornealis', 'Sneddon-Wilkinson disease']",8508,,48377,C0600336,,,1000771,D012872,694.1,,10042342,
mondo:0006615,sweat gland disorder,"['disease of sweat gland', 'sweat gland disease', 'sweat gland disease or disorder', 'disorder of sweat gland']",1383,,,C0038986,,,1000772,D013543,705.9,,,
mondo:0006616,toxicodendron dermatitis,"['contact dermatitis due to genus Toxicodendron', 'Rhus dermatitis']",3819,,,C0032342,,,1000773,D011040,692.6,,,
mondo:0006617,vesiculobullous skin disease,"['bullous skin diseases', 'pustular dermatoses, subcorneal', 'vesiculobullous dermatoses', 'vesiculobullous skin disease', 'dermatoses, bullous', 'skin diseases, vesicular', 'bullous dermatoses', 'skin disease, vesiculobullous', 'skin disease, vesicular', 'skin diseases, bullous', 'Sneddon-Wilkinson disease', 'pustular dermatosis, subcorneal', 'skin disease, bullous', 'dermatosis, subcorneal pustular', 'vesicular skin diseases', 'subcorneal pustular dermatoses', 'subcorneal pustular dermatosis', 'vesicular skin disease', 'dermatoses, vesiculobullous', 'vesiculobullous skin diseases', 'dermatoses, subcorneal pustular', 'bullous skin disease', 'Sneddon Wilkinson disease']",2731,,,C0037275,,,1000774,D012872,,,,
mondo:0006618,vibratory urticaria,,1554,,,C0157743,"['0.04114', '0.0941', '-0.4478', '0.2776', '-0.63', '-0.0727', '0.00825', '0.0886', '0.03943', '-0.04657', '-0.02834', '0.45', '0.2264', '-0.1714', '-0.2126', '0.1222', '-0.095', '-0.3774', '0.02232', '-0.0869', '0.2147', '-0.2688', '0.1252', '-0.02798', '0.1051', '-0.03427', '-0.04303', '-0.1179', '-0.2065', '-0.04263', '0.1223', '0.0997', '-0.02536', '-0.01171', '0.0461', '-0.09125', '-0.1771', '-0.1493', '0.2766', '-0.3083', '-0.05353', '-0.333', '0.0286', '-0.05392', '-0.00681', '0.1114', '-0.2006', '0.32', '0.0393', '0.06635', '-0.3354', '-0.3015', '-0.07996', '0.3228', '-0.05536', '-0.03662', '0.4414', '-0.53', '-0.4475', '0.1588', '0.04224', '0.05795', '-0.3242', '0.0931', '-0.3481', '-0.04745', '0.7266', '0.11206', '-0.1512', '0.546', '-0.1581', '0.1326', '-0.0382', '-0.4673', '0.3562', '0.3486', '-0.1798', '-0.03842', '0.0844', '0.1105', '-0.02147', '-0.02655', '0.3408', '0.2443', '0.0309', '0.2385', '-0.2869', '0.2153', '0.2588', '-0.177', '0.408', '0.2502', '-0.1094', '0.346', '0.616', '0.1573', '-0.278', '-0.253', '-0.7373', '0.2188']",,1000775,,708.4,L50.4,,
mondo:0006619,viral exanthem,,8672,,,C0153062,,,1000776,,057.9,,,
mondo:0006620,vulva fibroepithelial polyp,"['vulvar fibroepithelial polyp', 'fibroepithelial polyp of vulva', 'skin tag of mammalian vulva', 'vulvar fibroepithelial stromal polyp', 'vulval fibroepithelial polyp', 'fibroepithelial polyp of the vulva', 'mammalian vulva skin tag']",8255,,,C1336978,,C6857,1000777,,,,,
mondo:0006621,vulvar inverted follicular keratosis,"['mammalian vulva inverted follicular keratosis', 'inverted follicular keratosis of mammalian vulva']",6943,,,C1520084,,C40291,1000778,,,,,
mondo:0006622,vulvar seborrheic keratosis,"['seborrheic keratosis of mammalian vulva', 'seborrheic keratosis of vulva', 'seborrheic keratosis of the vulva', 'mammalian vulva seborrheic keratosis']",6944,,,C1336981,,C6375,1000779,,,,,
mondo:0006624,overactive bladder,"['overactive bladder', 'overactive bladder (disease)']",0070355,,,,,,1000781,D053201,596.51,,10020853,0000012
mondo:0006625,altitude sickness,,,,,,,,1000782,D000532,,,,
mondo:0006626,diabetic neuropathy,,9743,,,C0011882,,C26748,1000783,D003929,250.6,,,
mondo:0006629,"osteoarthritis, hip",['hip osteoarthritis'],,,,C0029410,,C34876,1000786,D015207,,,,
mondo:0006630,"osteoarthritis, spine",,,,,,,,1000787,D055013,,,,
mondo:0006631,"osteoarthritis, toe",,,,,,,,1000788,,,,,
mondo:0006632,"osteoarthritis, hand",,,,,,,,1000789,,,,,
mondo:0006633,acalculous cholecystitis,"['acute cholecystitis without calculus', 'cholecystitis without calculus', 'acute acalculous cholecystitis']",2828,,,C0267842,,C35578,1000790,D042101,,,10000347,
mondo:0006634,pituitary gland acidophil adenoma,"['eosinophil adenoma', 'pituitary gland acidophil adenoma', 'acidophil adenoma']",5392,,,C0001433,,C6780,1000791,D000239,,,,
mondo:0006635,Acinetobacter infectious disease,"['infection, Acinetobacter', 'infections, Mimae', 'Acinetobacter caused disease or disorder', 'infections, Acinetobacter', 'infection, Mimae', 'Mimae infections', 'Mimae infection', 'Acinetobacter infection']",3091,,,C0001139,,,1000792,D000151,,,,
mondo:0006636,Actinobacillus infectious disease,"['infections, Actinobacillus', 'infection, Actinobacillus', 'Actinobacillus infection', 'Actinobacillus caused disease or disorder']",,,,,,,1000793,D000189,,,,
mondo:0006637,acute kidney tubular necrosis,"['acute tubular necrosis', 'acute renal failure with lesion of tubular necrosis', 'acute renal failure with tubular necrosis', 'acute tubule necrosis', 'ATN - acute tubular necrosis']",12556,,,C0022672,,C34749,1000794,D007683,584.5,,10023441,0008682
mondo:0006638,acute retinal necrosis syndrome,['acute retinal necrosis'],3611,,,C0035319,,,1000795,D015882,,,,
mondo:0006639,adrenal cortex carcinoma,"['malignant adrenocortical tumour', 'adrenal cortical tumours', 'malignant tumor of adrenal cortex', 'adrenocortical carcinoma (disease)', 'adrenal cortical adenocarcinoma', 'ACC', 'malignant neoplasm of adrenal cortex', 'adrenal cortex carcinoma', 'adrenal cortical carcinoma (morphologic abnormality)', 'adrenocortical cancer', 'malignant tumour of adrenal cortex', 'malignant adrenocortical tumor', 'adrenal cortex adenocarcinoma', 'adenocarcinoma, adrenocortical, malignant', 'adrenocortical carcinoma', 'carcinoma of adrenal cortex', 'carcinoma, adrenocortical, malignant', 'adrenal cortex cancer', 'carcinoma of the adrenal cortex', 'adrenal cortical tumors', 'cancer of the adrenal cortex', 'adrenal cortical carcinoma', 'cortical cell carcinoma']",660,,1501,C0206686,"['-0.1053', '0.4976', '-0.3333', '-0.627', '0.3645', '0.2515', '0.3892', '0.4587', '-0.0752', '-0.3628', '0.03796', '0.2686', '-0.0747', '1.056', '-0.6914', '-0.75', '-0.3684', '-0.39', '-0.1838', '-0.2433', '-0.587', '-0.656', '0.902', '-0.626', '0.4336', '0.0494', '0.4482', '-0.2057', '-0.01642', '-0.2441', '0.9575', '0.1469', '0.5957', '-0.2666', '0.4426', '0.3992', '-0.713', '-0.1615', '-0.2338', '0.09094', '0.1511', '-0.1611', '0.10675', '-0.646', '0.355', '-0.04092', '-0.2717', '0.161', '0.1669', '0.11816', '0.775', '-0.1548', '0.0509', '-0.2815', '-0.3704', '0.0628', '0.1759', '-0.3496', '-0.2856', '0.3008', '0.3738', '0.589', '0.1432', '-0.4492', '-0.1887', '0.4548', '0.2764', '0.01006', '-0.1562', '0.3936', '-0.3281', '-0.1345', '0.2563', '0.2612', '0.2566', '-0.2212', '-0.5444', '-0.2197', '0.02628', '-0.859', '0.06805', '0.02545', '-0.3552', '-0.319', '-0.4526', '-0.1101', '0.05634', '-0.558', '0.4114', '-0.10406', '0.06537', '0.05838', '0.0348', '0.1696', '0.8105', '-0.7573', '0.1605', '-0.413', '0.1538', '-0.05527']",C9325,1000796,,,,10001388,0006744
mondo:0006640,adrenal gland hyperfunction,"['hyperfunction, adrenocortical', 'adrenocortical hyperfunction', 'hypercorticism', 'hypercortisolemia', 'hypercortisolism', 'hyperadrenalism', 'hyperfunction, adrenal gland', 'adrenal gland hyperfunction', 'hyperadrenocorticism']",3947,,,CN205287,,,1000797,D000308,255.3,,,0003118
mondo:0006641,afferent loop syndrome,,8438,,,C0001727,,,1000799,D000343,537.89,,10056245,
mondo:0006642,alcohol withdrawal delirium,"['alcohol withdrawal-induced delirium Tremens', 'alcohol withdrawal associated autonomic hyperactivity', 'alcohol withdrawal hallucinosis', 'autonomic hyperactivity, alcohol withdrawal associated', 'delirium, alcohol withdrawal', 'delirium Tremens', 'alcohol withdrawal induced delirium Tremens', 'delirium Tremens, alcohol withdrawal induced', 'hallucinosis, alcohol withdrawal']",,,,,,,1000800,D000430,291.0,,10001610,
mondo:0006643,alcoholic cardiomyopathy,"['alcohol-induced heart muscle disease', 'dilated cardiomyopathy secondary to alcohol', 'alcoholic cardiomyopathy']",12935,,,C0007192,,C53653,1000801,D002310,425.5,I42.6,10001616,
mondo:0006644,alcoholic liver cirrhosis,"['alcoholic cirrhosis', 'alcoholic cirrhosis of liver', 'portal cirrhosis', 'Laennec^s cirrhosis, alcoholic', 'Laennec^s cirrhosis']",14018,,,C1622502,,C34782,1000802,D008104,571.2,K70.3,10001618,
mondo:0006645,alcoholic polyneuropathy,"['alcoholic neuropathy', 'alcohol-related polyneuropathy']",14183,,,C0085677,,C26926,1000803,D020269,357.5,G62.1,,
mondo:0006646,angioleiomyoma,"['vascular leiomyoma', 'angiomyoma (morphologic abnormality)', 'angioleiomyoma', 'angiomyoma']",4265,,,C0206653,,C3747,1000806,D018229,,,,
mondo:0006647,anterior cerebral artery infarction,,3528,,,C0751843,,,1000807,D020243,,,,
mondo:0006648,anterior compartment of tibia syndrome,['anterior compartment syndrome'],3933,,,C0003152,,,1000808,D000868,,,,
mondo:0006649,anterior ischemic optic neuropathy,"['ischemic optic neuropathy', 'aion', 'ischaemic optic neuropathy', 'optic disc infarction leading to vision loss']",12010,,,C0155305,,,1000809,D018917,377.41,,10068250,
mondo:0006650,anterior spinal artery syndrome,['anterior spinal artery syndromic disease'],6712,,,C0221069,,,1000810,D020759,433.80,,10002703,
mondo:0006651,anterior uveitis,"['anterior uveitis', 'anterior uveitis (disease)', 'iridocyclitis']",1407,,280886,C0042165,,C35109,1000811,D014606,,,10002709,0012122
mondo:0006652,anterolateral myocardial infarction,"['infarction, anteroseptal myocardial', 'infarctions, anterolateral myocardial', 'anterolateral myocardial infarction', 'infarctions, anteroseptal myocardial', 'myocardial infarctions, anterolateral', 'myocardial infarction, anteroseptal', 'myocardial infarction, anterior wall', 'myocardial infarctions, anteroseptal', 'myocardial infarction, anterolateral', 'acute anterior wall myocardial infarction', 'anteroseptal myocardial infarctions', 'anterolateral myocardial infarctions', 'infarction, anterolateral myocardial', 'anteroseptal myocardial infarction']",5845,,,C0262564,,,1000812,D056988,,,10068109,
mondo:0006653,anthracosilicosis,,10324,,,C0003164,,C34389,1000813,D000874,,,10050363,
mondo:0006654,anthracosis,"['black lung', 'coal workers^ lung', 'coal workers^ pneumoconiosis', 'coal dust pneumoconiosis', 'coal miner^s pneumoconiosis', 'melanoedema']",10327,,,C0003165,,C34390,1000814,D055008,500,,10073051,
mondo:0006655,aortic valve prolapse,,5232,,,C0003505,,,1000815,D001023,,,10057454,
mondo:0006656,aortitis,['aorta inflammation'],519,,,C0003509,,C97085,1000816,D001025,,,10002921,
mondo:0006658,arteriolosclerosis,['arteriolosclerosis (morphologic abnormality)'],5162,,,C0878486,,C35543,1000819,D050379,,I70,,
mondo:0006659,arteriosclerosis obliterans,['arteriosclerosis obliterans (disorder) [ambiguous]'],5160,,,C0003851,,,1000820,D001162,440.8,,10065418,
mondo:0006660,arthus reaction,"['arthus reaction (function)', 'arthus reaction', 'arthus type urticaria', 'arthus phenomenon']",1556,,,C0003907,,C34400,1000821,D001183,995.21,,10003420,
mondo:0006662,aseptic meningitis,"['acute aseptic meningitis', 'aseptic meningitis']",12157,,,C0025290,,C118299,1000823,D008582,,,10003458,
mondo:0006663,perinatal asphyxia,"['perinatal depression', 'birth asphyxia', 'intrapartum asphyxia', 'asphyxia neonatorum', 'asphyxia - birth', 'hypoxia neonatorum', 'hypoxic and ischemic brain injury in the newborn', 'birth depression', 'neonatal hypoxic and ischaemic brain injury', 'fetal asphyxia', 'HIE', 'hypoxic-ischemic encephalopathy', 'postnatal asphyxia', 'hypoxic and ischaemic brain injury in the newborn', 'perinatal asphyxia', 'foetal asphyxia', 'asphyxia, in liveborn infant', 'perinatal hypoxia', 'neonatal hypoxic and ischemic brain injury']",11088,,137577,C0004045,,C116313,1000824,D001238,768.9,,,
mondo:0006664,atrial septal defect,"['congenital atrial septal defect', 'interauricular communication', 'interauricular septal defect', 'interatrial communication', 'atrioseptal defect', 'atrial septum defect', 'auricular septal defect', 'interatrial septal defect', 'ASD', 'atrial septal defect']",1882,,1478,C0018817,"['-0.09644', '-0.25', '-0.2815', '-0.2316', '0.279', '-0.2015', '0.4812', '1.108', '0.04132', '0.00184', '-0.1582', '-0.2107', '-0.0439', '0.2253', '-0.4534', '-0.577', '-0.4084', '-0.1674', '-0.1476', '-0.1895', '-0.3796', '0.2996', '0.7876', '0.232', '0.08484', '-0.1167', '0.0861', '0.082', '0.853', '0.3682', '0.2517', '0.255', '0.4912', '0.1554', '0.03156', '-0.2942', '0.624', '0.2233', '0.262', '-0.2812', '0.5146', '0.2101', '0.3748', '-0.1965', '0.06464', '0.159', '0.1788', '0.1224', '-0.2903', '0.4229', '-0.2072', '-0.2441', '-0.94', '-0.24', '-0.7217', '-0.04315', '-0.08435', '0.594', '-0.11957', '0.05096', '-0.3838', '0.4329', '0.6816', '0.03976', '-0.02425', '-0.6343', '0.9634', '0.3757', '-0.2085', '0.4878', '-0.04688', '0.1852', '0.5083', '-0.4805', '0.2927', '0.3865', '0.1694', '-0.6187', '-1.026', '0.06015', '-0.2837', '0.06586', '0.1904', '-0.03784', '0.1389', '-0.3652', '0.8174', '0.02728', '0.1711', '-0.4932', '-0.2365', '0.1387', '0.3945', '0.02904', '0.6978', '0.1043', '0.603', '-0.619', '-0.5156', '-0.1646']",C84473,1000825,D006344,,,10068864,
mondo:0006665,chronic atrophic gastritis,"['Gastritides, atrophic', 'atrophic gastritis', 'gastric atrophy', 'atrophic Gastritides']",8929,,,,,C7405,1000826,D005757,535.11,K29.4,10003685,
mondo:0006666,atrophy of thyroid,"['thyroid gland atrophy', 'thyroid atrophy']",,,,C2981141,,C26942,1000827,,246.8,,10043693,
mondo:0006668,bacterial conjunctivitis,"['purulent conjunctivitis', 'Bacteria caused conjunctival disease']",9700,,,C0009768,,C53656,1000829,D003234,372.03,,10061784,
mondo:0006669,bacterial endocarditis,"['bacterial endocarditis (disease)', 'bacterial endocarditis', 'Bacteria caused endocarditis (disease)']",,,,C0014121,,C128359,1000830,D004697,,,10004019,0006689
mondo:0006670,bacterial meningitis,"['Bacteria caused infectious meningitis', 'meningitis, bacterial']",9470,,,C0085437,,C118297,1000831,D016920,320.9,,10004049,
mondo:0006671,Bacteroides infectious disease,"['Bacteroides caused disease or disorder', 'infection, Bacteroides', 'Bacteroides infection', 'infections, Bacteroides']",,,,C0004669,,,1000832,D001442,041.84,,,
mondo:0006672,balanitis,"['glans penis inflammation', 'balanitis']",13033,,,C0004690,,C26705,1000833,D001446,,N48.1,10004073,
mondo:0006673,pituitary gland basophil adenoma,"['pituitary basophilic adenoma', 'pituitary gland basophilic adenoma', 'mucoid cell adenoma', 'basophilic pituitary gland adenoma', 'basophilic adenoma', 'basophil adenoma']",4542,,,C0001431,,C2856,1000834,D000237,,,,
mondo:0006676,beriberi,"['Beri Beri', 'vitamin B1 deficiency', 'thiamine deficiency']",13725,,,C0005122,,C34418,1000837,D001602,265.0,,10004482,
mondo:0006677,bile reflux,,12237,,,C0005403,,,1000838,D001655,,,,
mondo:0006678,bladder calculus,,11355,,,C0005683,,,1000839,D001744,594.1,,10005001,
mondo:0006679,bladder neck obstruction,['obstruction of bladder neck or vesicourethral orifice'],13948,,,C0005694,,,1000840,D001748,596.0,N32.0,10005053,
mondo:0006680,blue nevus,"['Jadassohn-Tièche syndrome', 'blue neuronevus', 'blue Nevus of the skin', 'blue skin Nevus', 'Tièche-Jadassohn nevus', 'benign mesenchymal melanoma', 'blue Nevus of skin', 'blue nevus', 'Jadassohn-TiC(che nevus', 'Jadassohn-Tièche nevus', 'Jadassohn-TiC(che syndrome']",,,,,,C3803,1000841,D018329,,,10062788,
mondo:0006681,Borrelia infectious disease,['Borrelia caused disease or disorder'],,,,C0006035,,,1000842,D001899,,,10061591,
mondo:0006682,brachial plexus neuritis,"['neuritis of brachial nerve plexus', 'brachial neuritis', 'brachial nerve plexus neuritis', 'acute shoulder neuritis', 'acute brachial radiculitis syndrome', 'parsonage Turner syndrome', 'parsonage-Aldren-Turner syndrome', 'acute brachial neuritis syndrome', 'idiopathic neuralgic amyotrophy', 'acute brachial neuritis']",3689,,,,,C84600,1000843,D020968,723.4,,10073002,
mondo:0006683,brachial plexus neuropathy,"['brachial plexopathy', 'peripheral neuropathy of brachial nerve plexus', 'brachial plexus disorder', 'brachial nerve plexus peripheral neuropathy']",3690,,,C0700251,,C27194,1000844,D020516,353.0,,,
mondo:0006684,brain edema,"['intracranial swelling', 'wet brain']",4724,,,,,,1000845,D001929,348.5,,10006121,
mondo:0006685,brain hypoxia - ischemia,,,,,,,,1000846,D020925,,,,
mondo:0006686,brain stem infarction,"['brainstem infarction', 'brainstem brain infarction', 'brain infarction of brainstem']",3523,,,C0521542,,,1000847,D020526,434.91,,,
mondo:0006687,burning mouth syndrome,"['stomatodynia', 'oral dysesthesia', 'BMS', 'Orodynia', 'Stomatopyrosis']",4331,,353253,CN242089,,C62545,1000850,D002054,,,10068065,
mondo:0006688,byssinosis,"['stripper^s asthma', 'flax-dressers^ disease', 'Monday morning fever', 'textile worker^s lung', 'cotton mill fever', 'cotton dust pneumoconiosis']",10323,,,C2242894,,C84605,1000851,D002095,504,J66.0,10006822,
mondo:0006690,carotid artery thrombosis,['carotid artery thrombosis'],3410,,,C0007274,,,1000853,D002341,433.10,,10007688,
mondo:0006692,central pontine myelinolysis,['osmotic demyelination syndrome'],636,,,C0206083,,C84623,1000857,D017590,341.8,G37.2,10007968,
mondo:0006693,cerebral arterial disease,,3527,,,C0007774,,,1000859,D002539,,,,
mondo:0006694,cerebral atherosclerosis,['cerebral atherosclerosis'],12720,,,C0007775,,C34459,1000860,D002537,437.0,I67.2,1008095,
mondo:0006696,cervix erosion,['erosion of cervix'],3456,,,C0007869,,,1000862,D002579,,,10015128,
mondo:0006698,cholecystolithiasis,,11151,,,C0947622,,,1000864,D041761,,,10049890,
mondo:0006699,choledocholithiasis,,11755,,,C0701818,,,1000865,D042883,,,10049891,
mondo:0006700,choroid cancer,"['malignant neoplasm of optic choroid', 'malignant neoplasm of choroid', 'malignant neoplasm of the choroid', 'cancer of optic choroid', 'choroidal tumor', 'optic choroid cancer', 'choroid neoplasm', 'malignant tumour of choroid', 'malignant optic choroid neoplasm', 'choroidal tumour', 'malignant tumor of the choroid', 'malignant tumour of the choroid', 'malignant choroid neoplasm', 'malignant choroid tumor', 'malignant tumor of choroid', 'malignant choroid tumour']",12759,,,,,C3566,1000866,D002830,190.6,,10057405,
mondo:0006701,chromophobe adenoma,"['pituitary chromophobe adenoma', 'pituitary gland chromophobe adenoma', 'chromophobe adenoma of the pituitary gland', 'chromophobe adenoma of pituitary gland']",3828,,,C0001432,,C2857,1000867,D000238,,,,
mondo:0006702,chronic inflammatory demyelinating polyradiculoneuropathy,"['CIDP', 'chronic relapsing polyneuropathy', 'chronic inflammatory demyelinating polyradiculoneuropathy']",5213,,2932,,,C84636,1000868,D020277,357.89,G61.81,10057645,
mondo:0006704,CNS demyelinating autoimmune disease,,,,,,,,1000870,D020278,,,,
mondo:0006705,Bacteroidaceae infectious disease,"['Bacteroidaceae infection', 'infections, Bacteroidaceae', 'Bacteroidaceae caused disease or disorder', 'infection, Bacteroidaceae']",,,,C0085392,,,1000872,D016866,,,,
mondo:0006706,Bifidobacteriales infectious disease,"['Bifidobacteriales caused disease or disorder', 'infection, Bifidobacteriales', 'Bifidobacteriales infection', 'infections, Bifidobacteriales']",,,,C1136339,,,1000873,D039941,,,,
mondo:0006708,Desulfovibrionaceae infectious disease,"['infections, Bilophila', 'Bilophila infection', 'infection, Desulfovibrio', 'Lawsonia infections', 'infection, Bilophila', 'Desulfovibrionaceae caused disease or disorder', 'infection, Lawsonia', 'infections, Desulfovibrionaceae', 'infections, Desulfovibrio', 'infection, Desulfovibrionaceae', 'Desulfovibrio infections', 'Desulfovibrionaceae infection', 'infections, Lawsonia', 'Bilophila infections', 'Desulfovibrio infection', 'Lawsonia infection']",,,,,,,1000875,D045824,,,,
mondo:0006709,common bile duct neoplasm,"['tumour of common bile duct', 'neoplasm of common bile duct', 'common bile duct tumor', 'common bile duct neoplasm (disease)', 'common bile duct tumour', 'tumor of common bile duct']",4608,,,C0009442,,,1000876,D003138,,,,
mondo:0006710,complex partial epilepsy,"['epilepsy, psychomotor', 'psychomotor epilepsy', 'Complex partial epileptic seizure']",12382,,,C0085417,,,1000877,D017029,345.40,,,
mondo:0006711,constrictive pericarditis,"['constrictive pericarditis', 'constrictive pericarditis (disease)']",11481,,,C0031048,,C78246,1000878,D010494,423.2,,10010783,0002563
mondo:0006712,corneal edema,['corneal edema'],11030,,,C0010037,,,1000879,D015715,371.20,,10011007,
mondo:0006713,corneal neovascularization,,11382,,,C0085109,,,1000880,D016510,370.60,,10011031,
mondo:0006714,coronary aneurysm,"['coronary artery aneurysm', 'arteriovenous aneurysm of coronary vessels', 'aneurysmal lesion of coronary artery', 'aneurysm of coronary vessels']",3362,,,C0010051,,,1000881,D003323,414.11,,10002348,0030882
mondo:0006715,coronary stenosis,['coronary artery stenosis'],4248,,,C0242231,,,1000882,D023921,,,10011089,
mondo:0006716,coronary thrombosis,"['coronary artery thrombosis', 'coronary vessel thrombotic disease', 'thrombotic disease of coronary vessel']",11847,,,C0010072,,,1000883,D003328,,I22,10011108,
mondo:0006717,cutaneous fibrous histiocytoma,"['fibrous xanthoma of skin', 'fibrous histiocytoma of skin', 'dermatofibroma, no ICD-O subtype', 'benign skin fibrous histiocytoma', 'fibrohistiocytic tumor', 'benign fibrous histiocytoma of the skin', 'fibrohistiocytic neoplasm', 'dermatofibroma, no ICD-O subtype (morphologic abnormality)', 'sclerosing angioma of skin', 'pleomorphic fibroma', 'fibrohistiocytic tumour', 'benign fibrous histiocytoma of skin', 'benign fibrous cutaneous histiocytoma', 'sclerosing angioma (morphologic abnormality)', 'benign cutaneous fibrous histiocytoma', 'sclerosing angioma', 'fibrous histiocytoma of the skin', 'dermatofibroma', 'DF', 'cutaneous fibrous histiocytoma']",4418,,,C0346049,,C6801,1000885,,,,,
mondo:0006718,cutaneous syphilis,['Treponema pallidum caused skin disease caused by bacterial infection'],,,,,,,1000887,D013591,,,,
mondo:0006720,"cystic, mucinous, and serous neoplasm",,,,,,,,1000889,D018297,,,,
mondo:0006721,de Quervain disease,"['radial styloid tenosynovitis', 'tenosynovitis, de Quervain^s']",14107,,,C0149870,,,1000891,D053684,727.04,,,
mondo:0006722,dental fluorosis,"['intrinsic enamel discolouration of fluorosis', 'mottled teeth', 'fluorosis', 'mottling of enamel']",13711,,,C0026618,,C85059,1000892,D009050,520.3,K00.3,10016819,
mondo:0006723,denture stomatitis,['denture sore mouth'],11875,,,C0038364,,,1000893,D013282,528.9,,,
mondo:0006726,diaphragmatic eventration,"['diaphragmatic eventration (disease)', 'diaphragmatic eventration']",10480,,,,,C98912,1000898,D003965,,,,0009110
mondo:0006727,diastolic heart failure,,9775,,,C1135196,,,1000899,D054144,428.30,,10069211,
mondo:0006729,discrete subaortic stenosis,,5804,,,C0012628,,,1000901,D021922,,,,
mondo:0006730,drug psychosis,"['drug-induced psychosis', 'drug-induced psychotic disorder']",1742,,,,,,1000902,D011605,292.1,,10045855,
mondo:0006731,drug-induced akathisia,,,,,,,,1000903,D017109,333.99,G25.71,10001540,
mondo:0006732,drug-induced dyskinesia,,,,,,,,1000904,D004409,333.99,,10013916,
mondo:0006733,dry eye syndrome,"['KCS', 'keratoconjunctivitis sicca', 'tear film insufficiency', 'dry eye(s)', 'dry eye syndrome', 'dry eye', 'eye(s), dry', 'sicca, keratoconjunctivitis']",12895,,,C0022575,,C34553,1001001,D015352,375.15,,100233350,
mondo:0006734,benign duodenal neoplasm,"['benign neoplasm of duodenum', 'benign tumor of duodenum', 'benign tumor of the duodenum', 'benign duodenal neoplasm', 'benign tumour of the duodenum', 'neoplasm of the duodenum', 'benign duodenal tumour', 'duodenal benign neoplasm', 'benign duodenal tumor', 'duodenum benign neoplasm', 'benign neoplasm of the duodenum', 'benign tumour of duodenum']",1737,,,,,C4775,1000907,D004379,,,10004251,
mondo:0006735,duodenogastric reflux,['duodenogastric reflux (finding)'],4071,,,C0013299,,,1000909,D004383,,,10060865,
mondo:0006736,dysplasia of cervix,,,,,C0007868,,,1000910,D002578,622.11,,10013957,
mondo:0006737,dystocia,,,,,,,,1000911,D004420,,,,
mondo:0006738,eccrine acrospiroma,"['acrospiroma, eccrine', 'Hidradrenoma, clear-cell', 'acrospiromas', 'Hidradrenomas, nodular', 'eccrine acrospiroma', 'nodular Hidradrenoma', 'poroma/acrospiroma', 'eccrine hidradenoma', 'acrospiromas, eccrine', 'eccrine Acrospiromas', 'clear-cell Hidradrenomas', 'poroma', 'nodular Hidradrenomas', 'solid cystic hidradenoma', 'poroma (acrospiroma)', 'Hidradrenomas, clear-cell', 'clear-cell Hidradrenoma', 'solid-cystic hidradenoma', 'eccrine poroma', 'Hidradrenoma, nodular', 'hidradenoma, solid-cystic', 'eccrine hidradenoma of skin', 'hidradenoma', 'Hidradenomas, solid-cystic', 'clear cell Hidradrenoma', 'solid-cystic Hidradenomas', 'Hidradenomas']",5442,,,,,C7568,1000912,D018250,,,,
mondo:0006739,Ehrlich tumor carcinoma,"['Ehrlich^s tumour', 'Ehrlich^s tumor']",5050,,,C0007125,,,1000913,D002286,,,,
mondo:0006740,empty sella syndrome,"['empty sella syndrome', 'empty sella', 'empty sella turcica']",3642,,,C0014008,,C84686,1000914,D004652,253.8,,10014567,
mondo:0006741,encephalomalacia,,2034,,,C0014068,,C98920,1000915,D004678,,,10051818,
mondo:0006742,endemic goiter,"['iodine-deficiency-related endemic goiter', 'iodine-deficiency-related endemic goitre', 'simple goitre', 'simple goiter']",13198,,,,,C35023,1000916,D006043,240.0,,10068848,
mondo:0006743,endocrine tuberculosis,,,,,C0041310,,,1000917,D014383,,,,
mondo:0006744,endolymphatic hydrops,['labyrinthine hydrops'],9848,,,C0206586,,,1000918,D018159,386.8,,10049934,
mondo:0006745,endometrioid stromal sarcoma,"['undifferentiated endometrial sarcoma', 'stromal sarcoma of the corpus uteri', 'ess', 'endometrioid stromal sarcoma', 'stromal sarcoma, endometrial, malignant', 'stromal sarcoma, endometrial', 'endometrial stromal sarcomas', 'endometrial stromal sarcoma, high grade', 'endometrial stromal sarcoma', 'sarcomas, endometrial stromal', 'stromal sarcomas, endometrial']",4226,,213711,C2239246,,C8973,1000919,D018203,,,10057649,
mondo:0006746,endomyocardial fibrosis,"['African endomyocardial fibrosis', 'obscure African cardiomyopathy', 'endomyocardial sclerosis']",12932,,,,,C34585,1000921,D004719,425.0,,10014800,
mondo:0006747,enterotoxemia,,,,,C0014371,,,1000922,D004767,799.89,,,
mondo:0006748,epilepsia partialis continua,,,,,,,,1000924,D017036,345.70,,10015034,
mondo:0006749,mixed epithelioid and spindle cell melanoma,['mixed epithelioid and spindle cell melanoma'],,,,,,C66756,1000925,D018332,,,,
mondo:0006751,Erysipelothrix infectious disease,"['Erysipelothrix caused disease or disorder', 'infections, Erysipelothrix', 'Erysipelothrix infection', 'infection, Erysipelothrix']",,,,C0014736,,,1000927,D004889,,,,
mondo:0006752,Erysipelothrix rhusiopathiae infectious disease,"['erysipeloid', 'Erysipelothrix rhusiopathiae caused disease or disorder']",0050061,,,C1276801,,,1000928,D004887,,A26,,
mondo:0006753,Escherichia coli meningitis,,,,,C0338395,,,1000929,D020814,320.82,,,
mondo:0006754,esophageal diverticulosis,,13185,,,C0917875,,,1000930,D045723,,,,
mondo:0006755,euthyroid sick syndrome,"['euthyroid sick syndrome', 'sick-euthyroid syndrome', 'sick euthyroid syndrome']",2856,,,C0015190,,C113170,1000931,D005067,790.94,E07.81,10015549,
mondo:0006757,extrahepatic cholestasis,"['extrahepatic bile duct cholestasis', 'extrahepatic cholestasis (finding)', 'cholestasis of extrahepatic bile duct', 'extrahepatic biliary stasis', 'extrahepatic obstructive biliary disease']",13619,,,C0005398,,,1000933,D001651,,,10008637,
mondo:0006758,female genital tuberculosis,,,,,,,,1000935,D014384,,,10061150,
mondo:0006759,femoral neuropathy,"['femoral nerve lesions', 'femoral nerve dysfunction', 'femoral nerve peripheral nerve lesion', 'peripheral nerve lesion of femoral nerve']",4196,,,C0751931,,C27595,1000936,D020428,355.2,,,
mondo:0006760,fetal erythroblastosis,"['erythroblastosis fetalis', 'HDFN', 'hemolytic disease of the foetus or newborn', 'isoimmune hemolytic disease of the newborn', 'hemolytic disease of the fetus or newborn', 'hemolytic disease of the newborn', 'EF - erythroblastosis foetalis', 'rhesus isoimmunisation of the newborn', 'haemolytic disease due to rhesus isoimmunisation']",1098,,,C0014761,,C101304,1000937,D004899,773.2,,,
mondo:0006761,fibromuscular dysplasia,"['FMDA', 'fibromuscular dysplasia of arteries', 'fibromuscular dysplasia']",,135580,336,C1851111,,C84714,1000938,D005352,,,10054794,
mondo:0006762,freemartinism,,4671,,,C0016697,,,1000939,D005611,,,,
mondo:0006763,frozen shoulder,"['adhesions-capsulitis,shoulder', 'adhesive capsulitis of shoulder', 'adhesive capsulitis']",14188,,,C0311223,,,1000941,D002062,726.0,M75.0,10017391,
mondo:0006764,fungal meningitis,['Fungi caused infectious meningitis'],11608,,,C0085438,,,1000942,D016921,321.1,,10017538,
mondo:0006765,Fusobacterium infectious disease,['Fusobacterium caused disease or disorder'],,,,C4039413,,,1000943,,041.84,,,
mondo:0006766,gait apraxia,['Gait apraxia (finding)'],4260,,,C1510417,,,1000944,D020235,,,10070635,
mondo:0006767,gastric antral vascular ectasia,['gave'],2493,,,,,C84724,1000945,D020252,,,10051585,
mondo:0006769,gastroparesis,"['gastroparalysis', 'gastroparesis', 'gastroparesis syndrome', 'gastroparesis (disease)', 'gastric atonia']",11914,,,C0152020,,,1000948,D018589,536.3,K31.84,10018043,0002578
mondo:0006770,giant cell reparative granuloma,"['GCLSB', 'central giant cell granuloma', 'central giant cell reparative granuloma of jaw', 'giant cell lesion of small bones', 'central giant cell (reparative) granuloma']",1866,,,C0162375,,C121893,1000950,D006101,526.3,,,
mondo:0006771,glossitis,['tongue inflammation'],1456,,,C0017675,,,1000951,D005928,529.0,K14.0,10018386,
mondo:0006773,gonadal tissue neoplasm,,,,,C0206722,,,1000953,D018309,,,,
mondo:0006774,habitual spontaneous abortion,,,,,,"['0.02603', '0.2622', '-0.074', '-0.02608', '0.157', '-0.0723', '0.01689', '0.2734', '-0.1702', '-0.0639', '-0.182', '0.06186', '0.06757', '0.0801', '-0.0684', '-0.0654', '-0.106', '0.0189', '-0.1073', '-0.2308', '-0.1525', '0.01554', '0.3716', '-0.1619', '-0.03677', '0.03375', '0.02728', '0.08417', '-0.01078', '0.02171', '0.206', '-0.2474', '0.1632', '0.1912', '-0.02254', '0.0806', '-0.1664', '-0.1803', '-0.1711', '-0.0844', '0.1274', '0.0374', '0.003504', '-0.2446', '-0.1688', '-0.1527', '-0.1149', '0.0994', '0.0888', '0.1848', '0.004143', '-0.2698', '-0.04733', '0.0869', '-0.1503', '0.03314', '0.1392', '-0.2139', '-0.2169', '-0.03818', '0.0661', '0.12494', '0.11804', '0.0599', '0.0247', '0.06714', '0.3425', '0.0088', '-0.3093', '0.09204', '-0.01267', '0.1785', '-0.0281', '-0.2294', '0.2131', '0.1037', '0.0393', '0.06995', '-0.12067', '-0.1427', '-0.1279', '0.1313', '-0.01445', '-0.00214', '0.04007', '0.01374', '0.2073', '0.1903', '0.2393', '-0.0956', '0.0369', '0.1443', '-0.0377', '0.0661', '0.2433', '0.04272', '-0.03494', '-0.3608', '0.0002904', '-0.04382']",,1000954,D000026,,,10062935,
mondo:0006777,hairy tongue,"['hairy Tongues', 'hairy tongue', 'overgrowth of filiform papillae', 'Tongues, hairy']",13500,,,C0040414,,C35075,1000957,D014064,529.8,,10043960,
mondo:0006778,halo nevus,"['leukoderma acquisitum Centrifugum of Sutton', 'halo nevi']",,,,C0474824,,C7602,1000958,D055882,709.09,,10062794,
mondo:0006779,heart aneurysm,['cardiac aneurysm'],9768,,,C0018789,,,1000959,D006322,414.19,I25.3,10002350,
mondo:0006780,heartwater disease,"['disease, heartwater']",,,,C0018835,,,1000960,D006357,,,,
mondo:0006781,Helicobacter pylori infectious disease,"['infection, Helicobacter', 'infections, Helicobacter', 'Helicobacter pylori infection, susceptibility to', 'Helicobacter infection', 'Helicobacter pylori caused disease or disorder']",,,,,,,1000961,D016481,,,,
mondo:0006782,hemometra,['hematometra'],9958,,,,,,1000962,D006409,621.4,N85.7,,
mondo:0006783,hemopneumothorax,,2718,,,C0019077,,,1000963,D006468,511.89,,10060632,
mondo:0006784,hemorrhagic disease of newborn,"['hemorrhagic disease of newborn', 'vitamin K deficiency bleeding in newborn']",,,,,,C111857,1000964,D006475,776.0,P53,10019601,
mondo:0006786,hepatic vein thrombosis,"['hepatic vein thrombosis', 'Budd-Chiari syndrome']",11512,,,,,,1000966,D006502,453.0,I82.0,10019713,
mondo:0006787,hidrocystoma,"['Hydrocystoma', 'cystadenoma', 'apocrine cystadenoma', 'apocrine/eccrine hidrocystoma', 'hidrocystoma', 'eccrine cystadenoma', 'hidrocystoma (morphologic abnormality)', 'eccrine hidrocystoma of skin']",3893,,,C0206672,,C3760,1000967,D018251,709.8,,10059019,
mondo:0006788,hydrophthalmos,,11212,,,,,,1000968,D006871,743.20,,,
mondo:0006789,hyperamylasemia,,,,,,,,1000969,D034321,,,10062777,
mondo:0006790,hypercementosis,['cementation hyperplasia'],12733,,,C0020441,,,1000970,D006936,521.5,K03.4,10020596,
mondo:0006791,hyperemesis gravidarum,"['pregnancy pernicious vomiting', 'hyperemesis gravidarum', 'hyperemesis gravidarum (disease)', 'pernicious vomiting of pregnancy']",,,,,,,1000971,D006939,,,10020614,0012188
mondo:0006792,hyperglobulinemic purpura,,3325,,,C0034151,,,1000972,D011694,,,,
mondo:0006793,hyperpituitarism,,2444,,,C0020506,,,1000973,D006964,253.1,,10020716,
mondo:0006794,hypersensitivity vasculitis,['leukocytoclastic vasculitis'],9809,,,,,C82863,1000974,,446.29,,10020764,
mondo:0006795,hypersplenism,"['hypersplenia', 'hypersplenism', 'hypersplenism (disease)']",6376,,,C0020532,,C34714,1000975,D006971,289.4,D73.1,10020769,0001971
mondo:0006796,hypertensive encephalopathy,,9427,,,C0151620,,C3503,1000976,D020343,437.2,I67.4,10020803,
mondo:0006797,hypertensive retinopathy,,11561,,,C0152132,,C3514,1000977,D058437,362.11,,10020839,
mondo:0006798,hypervitaminosis A,['hypervitaminosis type A'],9972,,,C0020579,,,1000978,D006986,278.2,E67.0,10020916,
mondo:0006799,hypothalamic neoplasm,"['hypothalamic tumor', 'tumor of the hypothalamus', 'tumour of hypothalamus', 'hypothalamus tumor', 'neoplasm of the hypothalamus', 'tumour of the hypothalamus', 'hypothalamus tumour', 'tumor of hypothalamus', 'hypothalamic tumour', 'neoplasm of hypothalamus', 'hypothalamic neoplasms']",3644,,,C0020659,,C3129,1000979,D007029,,,,
mondo:0006800,ideomotor apraxia,"['limb-kinetic apraxia (finding)', 'transcortical apraxia (finding)', 'ideomotor dyspraxia', 'classic apraxia (finding) [ambiguous]', 'limb-kinetic apraxia', 'transcortical apraxia', 'classic apraxia']",4627,,,,,,1000980,D020240,315.8,,10021216,
mondo:0006801,ileal neoplasm,"['neoplasm of the ileum', 'ileal tumor', 'ileal tumour', 'ileum neoplasm (disease)', 'ileum tumor', 'tumor of the ileum', 'tumour of the ileum', 'neoplasm of ileum', 'tumour of ileum', 'tumor of ileum', 'ileum tumour']",10156,,,C0020876,,C3130,1000981,D007078,,,,
mondo:0006802,inappropriate ADH syndrome,"['ectopic ADH secretion', 'syndrome of inappropriate secretion of antidiuretic hormone', 'ectopic antidiuretic hormone secretion', 'syndrome of inappropriate antidiuretic hormone', 'inappropriate Arginine vasopressin secretion', 'inappropriate antidiuretic hormone secretion syndrome', 'syndrome of inappropriate antidiuretic hormone secretion', 'syndrome of inappropriate secretion of ADH', 'SIADH', 'syndrome of inappropriate vasopressin secretion', 'inappropriate ADH secretion']",3401,,83449,C0021141,,C3988,1000982,D007177,253.6,,10042818,
mondo:0006803,inferior myocardial infarction,,5850,,,C0340305,,,1000983,D056989,,,10057546,
mondo:0006804,inflammatory breast carcinoma,"['inflammatory breast carcinoma', 'inflammatory carcinoma of breast', 'mastitis Carcinomatosa', 'mastitis carcinomatosa', 'IBC', 'inflammatory carcinoma of the breast', 'breast cancer, inflammatory', 'inflammatory breast cancer']",6263,,,C0278601,,C4001,1000984,D058922,,,10006205,
mondo:0006805,intermediate coronary syndrome,"['impending infarction', 'anginal chest pain at rest', 'angina at rest', 'unstable angina', 'worsening angina', 'Preinfarction angina']",8805,,,C0002965,,,1000985,D000789,411.1,I20.0,10022554,
mondo:0006806,intermediate uveitis,"['peripheral uveoretinitis', 'chronic cyclitis', 'pars planitis', 'intermediate uveitis (disease)', 'intermediate uveitis', 'IU']",12732,,279914,C0042166,,C35110,1000986,D015867,,,10022557,0012124
mondo:0006807,intestinal perforation,"['bowel perforation', 'perforation of intestine']",2074,,,C0021845,,C39611,1000987,D007416,777.6,,10022694,
mondo:0006808,intracranial arterial disease,,13089,,,C0752138,,,1000990,D020765,,,,
mondo:0006809,intracranial embolism,"['cerebral embolism with cerebral infarction', 'cerebral embolism']",4372,,,,,,1000991,D020766,434.10,,,
mondo:0006810,intracranial hypertension,['raised intracranial pressure'],9428,,,C0151740,,,1000992,D019586,,,10022764,
mondo:0006811,intracranial hypotension,,4723,,,C0524812,,,1000993,D019585,349.89,,10049977,
mondo:0006812,intracranial vasospasm,,13100,,,C0751895,,,1000994,D020301,,,,
mondo:0006813,intradermal nevus,['dermal Nevus'],,,,C0206737,,C3804,1000995,D018330,,,10058537,
mondo:0006814,iritis,"['iritis (disease)', 'iris inflammation', 'iritis']",1406,,,C0022081,,C50621,1000997,D007500,,,10022955,0001101
mondo:0006815,jejunal cancer,"['cancer of jejunum', 'malignant jejunum neoplasm', 'malignant tumour of jejunum', 'malignant neoplasm of jejunum', 'malignant tumor of jejunum', 'jejunum cancer']",13499,,,C0153427,,,1000998,,152.1,,10023166,
mondo:0006816,arthropathy,"['Joint ankylosis of the pelvic region and thigh', 'disease of skeletal joint', 'ankylosis of joint of lower leg', 'ankylosis of joint of shoulder region', 'ankylosis of forearm joint', 'ankylosis of hand joint', 'disorder of skeletal joint', 'Joint disorder', 'ankylosis of joint of pelvic region and thigh', 'ankylosis of joint of hand', 'ankylosis of ankle and foot joint', 'disorder, Joint', 'ankylosis of multiple joints', 'ankylosis of upper arm joint', 'ankylosis of joint of multiple sites', 'skeletal joint disease or disorder', 'Joint ankylosis of the forearm', 'skeletal joint disease', 'ankylosis of joint of ankle and/or foot', 'Joint ankylosis of the shoulder region', 'infectious arthropathy', 'Joint ankylosis of the ankle and foot', 'ankylosis of lower leg joint', 'ankylosis of joint of upper arm', 'arthropathy', 'Joint ankylosis of the upper arm', 'Joint ankylosis of the hand', 'Joint ankylosis of the lower leg', 'ankylosis of joint of forearm', 'Joint ankylosis of the ankle and/or foot']",381,,,C0022408,,C35760,1000999,D007592,719.98,,10003285,
mondo:0006817,juxtacortical osteosarcoma,"['juxtacortical osteogenic sarcoma', 'parosteal osteosarcoma', 'juxtacortical osteosarcoma', 'PAOS', 'parosteal osteogenic sarcoma']",3373,,,C0206642,,C8969,1001000,D018217,,,,
mondo:0006820,kidney cortex necrosis,['renal cortical necrosis'],2973,,,,,,1001003,D007673,583.6,,10023414,
mondo:0006821,kidney papillary necrosis,"['necrotizing renal papillitis', 'papillary necrosis', 'renal papillitis necrotizing']",2981,,,C0022667,,,1001004,D007681,583.7,,10028865,
mondo:0006823,Klinefelter syndrome,"['XXY trisomy', 'Klinefelter syndrome', 'Klinefelter^s syndrome', 'Klinefelter^s syndrome, XXY', '47,XXY syndrome', 'XXY syndrome', 'hypogonadotropic hypogonadism', 'XXY syndrome (Klinefelter syndrome)']",1921,,,C0022735,,C34752,1001006,D007713,758.7,,10023463,
mondo:0006824,Krebs 2 carcinoma,,,,,C0007128,,,1001007,D002287,,,,
mondo:0006825,kuru,['kuru encephalopathy'],648,,454745,C0022802,,,1001008,D007729,046.0,A81.81,10023497,
mondo:0006826,kwashiorkor,"['nutritional oedema with dyspigmentation of skin and/or hair', 'nutritional oedema with dyspigmentation of skin and hair', 'nutritional edema with dyspigmentation of skin and hair', 'nutritional edema with dyspigmentation of skin and/or hair', 'Kwashiokor']",13579,,,C0022806,,,1001009,D007732,260,E40,10023504,
mondo:0006827,lateral medullary syndrome,"['PICA syndrome', 'Vertebral artery syndrome', 'Posterior inferior cerebellar artery syndrome', 'Lateral medullary syndrome', 'Wallenberg^s syndrome', 'Wallenberg syndrome']",3522,,,C0043019,,C84807,1001011,D014854,437.1,,10024033,
mondo:0006828,nasal cavity and paranasal sinus lethal midline granuloma,"['Midline lethal granuloma of the nasal cavity and paranasal sinus', 'malignant granuloma of face', 'midfacial Necrotising lesion', 'lethal midline granuloma', 'nasal cavity and paranasal sinus lethal Midline granuloma', 'Midline lethal granuloma of nasal cavity and paranasal sinus']",9072,,,,,C8196,1001013,D006103,446.3,,10024255,
mondo:0006829,leukemoid reaction,,,,,C0023501,,,1001014,D007955,288.8,D72.823,10024373,
mondo:0006830,leukoplakia of penis,"['kraurosis of penis', 'penile leukoplakia', 'leukoplakia of the penis', 'kraurosis penis']",8738,,,C0022782,,C3151,1001015,,607.0,,10024394,
mondo:0006831,leukostasis,['leukostasis (morphologic abnormality)'],12986,,,C0282548,,,1001016,D018921,,,10024404,
mondo:0006833,lingual goiter,,13196,,,C0271760,,,1001018,D047268,759.2,,,
mondo:0006834,lip cancer,"['malignant tumor of lower labial mucosa', 'malignant tumour of labial mucosa', 'malignant tumor of the Lip', 'malignant tumour of the Lip', 'malignant tumour of lip', 'malignant tumour of lower labial mucosa', 'malignant neoplasm of lip, inner aspect', 'lip cancer', 'malignant neoplasm of lower lip, mucosa', 'malignant tumour of Lip', 'malignant neoplasm of lower lip, inner aspect', 'malignant neoplasm of commissure of lip', 'malignant Lip tumor', 'cancer of lip', 'malignant tumor of Lip', 'malignant neoplasm of external Lip, not specified as upper or lower', 'malignant neoplasm of Lip', 'malignant neoplasm of vermilion border of lip', 'malignant lip neoplasm', 'malignant neoplasm of other sites of lip', 'malignant tumor of commissure of lip', 'malignant neoplasm of lip, unspecified', 'malignant tumor of labial mucosa', 'malignant tumor of labial commissure', 'malignant neoplasm of lower lip, oral aspect', 'malignant neoplasm of lower lip, buccal aspect', 'malignant neoplasm of oral aspect of lip, not specified whether upper or lower', 'malignant neoplasm of labial commissure of lip', 'malignant neoplasm of lip, unspecified, vermilion border', 'malignant tumour of labial commissure', 'malignant tumour of commissure of lip', 'malignant neoplasm of lip, external', 'malignant tumor of lip', 'malignant neoplasm of lip, unspecified, inner aspect', 'malignant neoplasm of lip', 'malignant Lip neoplasm', 'malignant Lip tumour', 'malignant neoplasm of lip, vermilion border', 'malignant neoplasm of the Lip']",8564,,,,,C7485,1001019,D008048,140.8,C00,10007089,
mondo:0006835,lipoid nephrosis,"['minimal change nephrotic syndrome', 'MCNS', 'minimal change disease', 'minimal change glomerulonephritis', 'nephrotic syndrome with lesion of minimal change nephrotic syndrome', 'nil disease', 'minimal change glomerulopathy', 'idiopathic minimal change nephrotic syndrome', 'lipoid nephrosis', 'minimal change nephropathy', 'nephrotic syndrome with lesion of minimal change glomerulonephritis']",10966,,,C0027721,,C34844,1001020,D009402,,,10058325,
mondo:0006836,Listeria meningitis,"['Listeria monocytogenes meningitis', 'Meningitides, Listeria', 'Listeria Meningoencephalitides', 'Meningitides, Listeria monocytogenes', 'Listeria monocytogenes caused infectious meningitis', 'meningoencephalitis, Listeria', 'Meningoencephalitides, Listeria', 'cerebritis, Listeria', 'Listeria Cerebritides', 'Listeria meningitis', 'Listeria Meningitides', 'Listeria monocytogenes Meningitides', 'Cerebritides, Listeria', 'meningitis, Listeria monocytogenes', 'Listeria cerebritis', 'Listeria meningoencephalitis']",11572,,,C0025293,,,1001021,D008584,320.7,,,
mondo:0006837,low tension glaucoma,"['tension glaucoma, normal', 'glaucoma, normal tension', 'tension Glaucomas, Low', 'Glaucomas, normal tension', 'normal tension glaucoma', 'tension glaucoma, Low', 'low tension Glaucomas', 'normal tension Glaucomas', 'tension Glaucomas, normal', 'glaucoma, Low tension', 'Glaucomas, Low tension']",13544,,,C0152136,,,1001022,D057066,365.12,,10024931,
mondo:0006838,lupus vulgaris,,,,,C0024131,,,1001023,D008177,,,10025143,
mondo:0006839,Lutembacher syndrome,"['Lutembacher syndrome', 'syndrome, Lutembacher', 'Lutembacher^s anomaly', 'Lutembacher^s syndrome', 'syndrome, Lutembacher^s', 'Lutembachers syndrome']",1998,,,C0024164,,,1001024,D008185,,,,
mondo:0006840,lymphangiectasis,['lymphangiectasia'],,,,C0024214,,C97087,1001025,D008200,,,,
mondo:0006841,lymphangioendothelioma,['acquired progressive lymphangioma'],,,,,,C3203,1001026,,,,,
mondo:0006842,lymphangiomyoma,"['lymphangioleiomyoma', 'lymphangiomyoma']",,,,C0024223,,C3204,1001027,D008203,,,,
mondo:0006843,macular holes,['macular hole'],7633,,,C0024441,,C34795,1001028,D012167,,,,
mondo:0006844,magnesium deficiency,,,,,C0024473,,,1001029,D008275,,E61.2,10025433,
mondo:0006845,male genital tuberculosis,"['genital Tuberculoses, Male', 'male reproductive system tuberculosis', 'Male genital Tuberculoses', 'genital tuberculosis, Male', 'Tuberculoses, Male genital', 'male genital tuberculosis']",,,,C0041317,,,1001030,D014389,,,10061234,
mondo:0006846,malignant hypertension,"['MHT', 'hypertensive emergency', 'malignant phase hypertension', 'accelerated-malignant hypertension']",10824,,,C0745136,,,1001031,D006974,,,10025600,
mondo:0006847,malignant lymphatic vessel tumor,,,,,,,,1001032,,,,,
mondo:0006848,marasmus,"['nutritional atrophy', 'nutritional marasmus']",12328,,,C0086588,,,1001033,,261,E41,10026820,
mondo:0006849,mastitis,"['breast infection', 'breast inflammation', 'inflammatory breast disease', 'inflammatory disease of breast']",10690,,,C0392317,,C53662,1001034,D008413,,,10026883,
mondo:0006850,maxillary sinus neoplasm,"['neoplasm of the maxillary sinus', 'maxillary sinus tumour', 'tumour of the maxillary antrum', 'tumor of maxillary sinus', 'maxillary sinus neoplasm', 'maxillary antrum tumour', 'tumour of maxillary sinus', 'neoplasm of maxillary sinus', 'tumor of the maxillary antrum', 'tumor of the maxillofacial sinus', 'tumour of the maxillofacial sinus', 'tumor of the maxillary sinus', 'neoplasm of maxillofacial sinus', 'maxillary antrum neoplasm', 'maxillary sinus neoplasm (disease)', 'maxillary antrum tumor', 'tumour of maxillary antrum', 'neoplasm of the maxillofacial sinus', 'tumor of maxillary antrum', 'maxillofacial sinus tumor', 'maxillofacial sinus tumour', 'tumor of maxillofacial sinus', 'tumour of maxillofacial sinus', 'neoplasm of the maxillary antrum', 'maxillofacial sinus neoplasm', 'neoplasm of maxillary antrum', 'maxillary sinus tumor', 'tumour of the maxillary sinus']",1358,,,C0024958,,C3219,1001035,D008444,,,10026130,
mondo:0006851,meconium aspiration syndrome,"['neonatal aspiration of meconium', 'meconium aspiration', 'meconium inhalation', 'syndrome, meconium aspiration', 'aspiration, meconium', 'aspiration syndrome, meconium', 'meconium aspiration syndrome', 'MAS']",11049,,70588,C0025048,,C87093,1001037,D008471,770.1,,10027057,
mondo:0006853,mesenchymal chondrosarcoma,['mesenchymal chondrosarcoma'],4545,,,C0206637,,C3737,1001041,D018211,,,10027389,
mondo:0006854,mesenchymoma,['mesenchymoma'],2668,,,C0025464,,C3233,1001042,D008637,,,,
mondo:0006855,mesenteric vascular occlusion,,13252,,,C0025472,,,1001043,D008641,,,10074583,
mondo:0006856,mesothelial neoplasm,"['mesothelial tumour', 'mesothelial neoplasm', 'mesothelial tumor']",,,,C3714739,,C3786,1001044,D018301,,C45-C49,,
mondo:0006857,middle cerebral artery infarction,,3525,,,C0740392,,,1001045,D020244,,,,
mondo:0006858,mouth disorder,"['oral disorder', 'disease of mouth', 'mouth disease or disorder', 'mouth disease', 'disorder of mouth', 'oral disease']",403,,,C0026636,,C3240,1001047,D009059,528.9,,,
mondo:0006859,mucinous cystadenoma,"['adenoma, mucinous, benign', 'mucinous cystadenoma', 'pseudomucinous cystadenoma', 'mucinous adenoma', 'mucinous cystoma']",,,,C0010635,,C2973,1001048,D018291,,,,
mondo:0006861,myeloid sarcoma,"['sarcoma, myeloid, malignant', 'chloroma', 'myeloid sarcoma', 'granulocytic sarcoma', 'MS', 'extramedullary myeloid tumor', 'extramedullary myeloid tumour']",8683,,86850,,,C3520,1001052,D023981,205.3,C92.3,10028562,
mondo:0006862,myofascial pain syndrome,,431,,,C0027073,,,1001054,D009209,729.1,,10048780,
mondo:0006863,myxosarcoma,"['myxosarcoma', 'myxosarcoma (morphologic abnormality)', 'myxosarcoma, malignant']",4136,,,C0027155,,C3255,1001056,D009236,,,,
mondo:0006864,necrotizing sialometaplasia,,12901,,,C0037033,,,1001057,D012797,527.8,,10072176,
mondo:0006865,necrotizing ulcerative gingivitis,"['Vincent^s disease', 'Vincent angina', 'Fusospirillosis', 'phagedenic gingivitis', 'acute necrotising ulcerative gingivitis', 'acute membranous gingivitis', 'acute necrotizing ulcerative gingivostomatitis', 'acute necrotising ulcerative gingivostomatitis [ambiguous]', 'angina - Vincents', 'early acute necrotising gingivitis', 'Vincent^s infection, any site', 'acute necrotising ulcerative gingivitis [ambiguous]', 'Fusospirillary gingivitis', 'acute necrotising ulcerative gingivostomatitis', 'Vincent^s gingivitis', 'Vincent^s infection', 'acute necrotizing ulcerative gingivitis', 'Vincent^s stomatitis', 'acute ulceromembranous gingivitis', 'Vincent^s angina - pharyngitis', 'Vincent^s angina', 'ANUG', 'trench mouth']",13924,,,C0017575,,C34637,1001058,D005892,101,,,
mondo:0006866,neonatal myasthenia gravis,['neonatal myasthenia gravis'],14043,,,,,,1001059,D020941,775.2,,10028963,
mondo:0006868,neurogenic bowel,,13419,,,C0695242,,,1001061,D055496,564.81,,10048657,
mondo:0006869,nodular goiter,"['nodular goiter (disease)', 'nodular goiter', 'nodular goitre NOS', 'nodular goitre (disease)', 'goiter, nodular']",13197,,,C0018023,,C131437,1001062,D006044,,,10018495,0005994
mondo:0006871,non-gestational choriocarcinoma,,4320,,,C1135873,,,1001064,D031954,,,,
mondo:0006873,nutritional deficiency disease,['malnourished'],5113,,,,,C3669,1001067,D003677,269.9,E40-E46,10046058,
mondo:0006874,obstructive jaundice,"['cholestatic jaundice syndrome', 'cholestatic jaundice', 'obstructive hyperbilirubinemia']",13603,,,C0022354,,,1001068,D041781,,,10029982,
mondo:0006875,ocular hypertension,,9282,,,C0028840,,,1001069,D009798,365.04,,10030043,
mondo:0006876,ocular tuberculosis,,0070344,,,C0041322,,,1001070,D014392,017.32,,,
mondo:0006877,oophoritis,['ovary inflammation'],10974,,,C0029051,,,1001071,D009869,,,10030345,
mondo:0006878,Moraxellaceae infectious disease,"['infection, Psychobacter', 'infection, Moraxella', 'infections, Moraxella', 'infections, Psychobacter', 'Moraxella infections', 'Psychobacter infection', 'Moraxella infection', 'infection, Moraxellaceae', 'infections, Moraxellaceae', 'Moraxellaceae infection', 'Psychobacter infections', 'Moraxellaceae caused disease or disorder']",,,,,,,1001072,D045828,,,,
mondo:0006879,optic papillitis,"['edema, retinal', 'retinal Edemas', 'Edemas, optic disk', 'retinal edema', 'edema, optic disk', 'edema of the optic disk', 'optic disk inflammation', 'Choked disks', 'disks, Choked', 'disk, Choked', 'Choked disc', 'Edemas, optic disc', 'optic papilla oedema', 'Choked disk', 'optic disc inflammation', 'inflammation of optic disc', 'optic disc oedema', 'optic discitis', 'papilledema associated with decreased intraocular pressure', 'papillitis, optic', 'papillitis, optic nerve', 'edema, optic papilla', 'Edemas, retinal', 'optic disk edema', 'oedema of the optic disc', 'optic papillitis', 'papillitis', 'Choked discs', 'edema, optic disc', 'increased intracranial pressure-associated papilledema', 'optic nerve papillitis', 'increased intracranial pressure associated papilledema', 'optic papilla edema', 'papilledema associated with increased intracranial pressure', 'retinal oedema', 'decreased intraocular pressure associated papilledema', 'decreased intraocular pressure-associated papilledema']",10175,,,,,,1001074,,377.31,,10030948,
mondo:0006880,oral leukoedema,['leukedema of mouth'],4557,,,C0023523,,,1001075,D007967,528.79,,10057365,
mondo:0006881,orbital cellulitis,['orbital cellulitis'],11234,,,C0149507,,C99000,1001076,D054517,376.01,,10031036,
mondo:0006882,orchitis,"['Inflammation of testis', 'orchitis (disease)', 'orchitis', 'Orchititis', 'testis inflammation', 'testisitis']",2518,,,C0029191,,C97145,1001078,D009920,,N45.2,10031064,0100796
mondo:0006883,malignant superior sulcus neoplasm,"['malignant Superior sulcus tumor of the lung', 'Pancoast^s syndrome', 'malignant Superior sulcus tumour', 'malignant Superior sulcus neoplasm', 'pulmonary sulcus neoplasm, malignant', 'superior pulmonary sulcus syndrome', 'Pancoast tumor', 'pulmonary sulcus tumour', 'malignant Superior sulcus tumour of lung', 'malignant Superior sulcus lung neoplasm', 'malignant Superior sulcus neoplasm of lung', 'superior sulcus tumour', 'malignant Superior sulcus tumour of the lung', 'malignant Superior sulcus neoplasm of the lung', 'Pancoast^s tumour', 'malignant Superior sulcus tumor of lung', 'malignant Superior sulcus lung tumor', 'superior pulmonary sulcus syndrome (disorder) [ambiguous]', 'Pancoast tumour', 'malignant Superior sulcus lung tumour', 'malignant Superior sulcus tumor', 'Pancoast^s tumor']",8007,,,C0549471,,C7527,1001080,D010178,,,,
mondo:0006884,panophthalmitis,,13732,,,C0030332,,,1001081,D010202,360.02,,10033683,
mondo:0006886,thyroid gland papillary and follicular carcinoma,"['papillary and follicular carcinoma', 'thyroid gland papillary and follicular carcinoma', 'papillary and follicular adenocarcinoma', 'papillary follicular thyroid adenocarcinoma']",3968,,,C0206683,,C7380,1001083,D018265,,,,
mondo:0006887,parametritis,"['pelvic cellulitis', 'parametrium inflammation']",1260,,,C0030455,,,1001084,D010249,,,,
mondo:0006888,paraneoplastic polyneuropathy,['paraneoplastic polyneuropathy'],8681,,,C0270932,,C3981,1001085,D020364,357.3,,10062289,
mondo:0006889,paraphimosis,,5334,,,C0030483,,C34893,1001086,D010263,,N47.2,10033890,
mondo:0006890,parathyroid gland adenoma,"['adenoma of parathyroid gland', 'adenoma of parathyroid', 'adenoma of the parathyroid gland', 'parathyroid gland adenoma', 'adenoma of the parathyroid', 'parathyroid adenoma']",7608,,,C0262587,,C3916,1001087,,,,10033940,0002897
mondo:0006891,partial motor epilepsy,"['focal motor seizure', 'epilepsy, focal motor']",3327,,,,,,1001089,D020938,780.39,,,
mondo:0006892,partial sensory epilepsy,,3330,,,,,,1001090,D020937,,,,
mondo:0006893,Pasteurella hemorrhagic septicemia,"['bacteremia, hemorrhagic', 'haemorrhagic septicemia', 'bacteremia, haemorrhagic', 'haemorrhagic bacteremia', 'Septicaemia, hemorrhagic', 'septicemia, hemorrhagic', 'septicemia, haemorrhagic', 'Septicaemia, haemorrhagic', 'hemorrhagic bacteremia', 'haemorrhagic Septicaemia', 'hemorrhagic Septicaemia']",,,,,,,1001091,D006483,,,,
mondo:0006894,patellofemoral pain syndrome,,14284,,,C0877149,,,1001092,D046788,,,10049143,
mondo:0006895,penile neoplasm,"['penis neoplasm (disease)', 'tumour of penis', 'neoplasm of the penis', 'penis tumour', 'penis tumor', 'neoplasm of penis', 'penile neoplasms', 'tumour of the penis', 'penile tumour', 'tumor of penis', 'penile neoplasm', 'penile tumor', 'tumor of the penis']",11624,,,C0030849,,C3317,1001094,D010412,239.5,,10061913,
mondo:0006896,peptic esophagitis,"['peptic reflux disease', 'peptic esophagitis', 'reflux oesophagitis', 'reflux esophagitis']",13976,,,C0014869,,,1001095,D004942,530.11,,,
mondo:0006897,periapical granuloma,"['apical granuloma', 'periapical granuloma']",4617,,,C0031029,,,1001096,D010484,,,10060985,
mondo:0006898,periarthritis,,2964,,,C0031037,,,1001097,D010489,,,10034464,
mondo:0006899,pericoronitis,,3671,,,C0031055,,,1001098,D010497,,,10034504,
mondo:0006900,perinephritis,['perirenal fat inflammation'],2982,,,C0031065,,,1001099,D010501,,,10072058,
mondo:0006901,peritoneal neoplasm,"['tumor of peritoneum', 'tumour of peritoneum', 'peritoneum tumour', 'peritoneum tumor', 'neoplasm of peritoneum', 'peritoneum neoplasm (disease)', 'peritoneal neoplasm']",,,,,,C3322,1001100,D010534,,,10061344,
mondo:0006903,peroneal nerve paralysis,"['peroneal nerve palsy', 'palsy, peroneal nerve', 'nerve palsy, peroneal']",6925,,,C0270810,,C27061,1001102,D020427,,,10033828,
mondo:0006904,phimosis,"['tight foreskin', 'tight frenulum']",2712,,,,,C26852,1001104,D010688,,N47.1,10034878,
mondo:0006905,pigmented spindle cell nevus,['spindle cell Nevus of Reed'],,,,,,C4751,1001105,D018331,,,,
mondo:0006907,pilar sheath acanthoma,"['acanthoma of the Pilar sheath', 'Infundibuloisthmicoma', 'Pilar sheath acanthoma', 'acanthoma of Pilar sheath']",4322,,,C0346005,,C4468,1001107,,,,,
mondo:0006908,pituitary apoplexy,['pituitary gland apoplexy'],1129,,95613,C0032001,,C26853,1001108,D010899,253.8,,10056447,
mondo:0006909,pituitary dwarfism,,,,,C0013338,,,1001109,D004393,253.3,,10035083,
mondo:0006912,pneumatosis cystoides intestinalis,,13249,,,C0032266,,,1001113,D011006,569.89,,10049732,
mondo:0006913,pneumococcal meningitis,['Streptococcus pneumoniae caused infectious meningitis'],,,55655,C0025295,,C157958,1001114,D008586,320.1,G00.1,10035645,
mondo:0006915,polyradiculoneuropathy,,4308,,,C0032587,,,1001116,D011129,,,,
mondo:0006916,postcholecystectomy syndrome,,9740,,,C0152099,,,1001117,D017562,576.0,K91.5,,
mondo:0006917,posterior cerebral artery infarction,,3821,,,C0752132,,,1001118,D020762,,,,
mondo:0006918,posterior uveitis,"['chorioretinal region inflammation', 'uveitis, posterior', 'inflammation of chorioretinal region']",12574,,280892,C0042167,,C35111,1001119,D015866,,,10036370,
mondo:0006919,potassium deficiency,,,,,,,,1001120,D011191,,,10036445,
mondo:0006920,prediabetes syndrome,"['prediabetic state', 'borderline diabetes', 'prediabetes']",11716,,,C0362046,,C122685,1001121,D011236,,,10065542,
mondo:0006921,Actinomycetales infectious disease,"['infections, actinomycetales', 'infection, actinomycete', 'infection, actinomycetales', 'infection caused by actinomycetales', 'actinomycetales infection', 'infections, actinomycete', 'actinomycotic infectious disease', 'actinomycetales caused disease or disorder', 'actinomycete infections', 'actinomycete infection', 'actinomycetales infections']",,,,C0001255,,C84534,1001122,D000193,039.9,,,
mondo:0006922,Anaplasmataceae infectious disease,"['infections, Anaplasmataceae', 'Anaplasmataceae infection', 'Anaplasmataceae caused disease or disorder', 'infection, Anaplasmataceae', 'Haemobartonellosis', 'Haemobartonelloses']",,,,,,,1001123,D000711,,,,
mondo:0006923,Bacillaceae infectious disease,"['infection, Bacillaceae', 'Bacillaceae infection', 'infections, Bacillaceae', 'Bacillaceae caused disease or disorder']",,,,C0085389,,,1001124,D016863,,,,
mondo:0006924,Bartonellaceae infectious disease,"['Bartonellaceae infection', 'Bartonellaceae caused disease or disorder', 'infection, Bartonellaceae', 'infections, Bartonellaceae']",,,,C0004773,,,1001125,D001476,,,,
mondo:0006925,Fusobacteriaceae infectious disease,"['Fusobacteriaceae caused disease or disorder', 'infections, Fusobacteriaceae', 'infection, Fusobacteriaceae', 'Fusobacteriaceae infection']",,,,C1258222,,,1001126,D045825,,,,
mondo:0006926,haemophilus infectious disease,"['Hemophilus infections', 'Hemophilus infection', 'infection, Hemophilus', 'infections, Haemophilus', 'Haemophilus caused disease or disorder', 'infections, Hemophilus', 'Haemophilus infection', 'infection, Haemophilus']",,,,,,C34654,1001127,D006192,,,,
mondo:0006927,Rickettsiaceae infectious disease,"['infection, Rickettsiaceae', 'Rickettsiaceae infection', 'rickettsialpox', 'infections, Rickettsiaceae', 'Rickettsiaceae caused disease or disorder']",,,,,,,1001128,D012288,,,,
mondo:0006929,Proteus infectious disease,"['infection, Proteus', 'infections, Proteus', 'Proteus infection', 'Proteus <enterobacteria> caused disease or disorder']",,,,C0033700,,,1001130,D011512,,,,
mondo:0006930,pseudobulbar palsy,"['pseudobulbar palsy', 'pseudobulbar paralysis']",12680,,,C0033790,,C129934,1001131,D020828,335.23,,10037114,
mondo:0006931,pulmonary coin lesion,"['coin lesion of lung (context-dependent category)', 'coin lesion of lung', 'coin lesion of lung (finding)', 'coin lesion lung']",5364,,,C0009250,,,1001133,D003074,,,,
mondo:0006932,pulmonary edema,"['edema, pulmonary']",11396,,,C0034063,,C26868,1001134,D011654,,J81,10037375,
mondo:0006933,pulmonary plasma cell granuloma,"['granuloma, plasma cell, pulmonary', 'lymphocytic pseudotumor of lung', 'sclerosing hemangiocytoma of lung']",3677,,,C0085269,,,1001135,D016726,518.89,,,
mondo:0006935,pulmonary subvalvular stenosis,"['congenital infundibular stenosis', 'pulmonary infundibular stenosis', 'infundibular pulmonic stenosis, congenital', 'infundibular pulmonic stenosis', 'subvalvular pulmonic stenosis']",8861,,,,,C34961,1001137,D011662,746.83,,,
mondo:0006936,pulmonary valve stenosis,,6420,,,,,,1001138,D011666,,,10037450,
mondo:0006937,pulpitis,['dental pulp inflammation'],11121,,,C0034103,,,1001139,D011671,522.0,K04.0,10037463,
mondo:0006938,pyelitis,['renal pelvis inflammation'],2744,,,C0034183,,C34964,1001140,D011702,,,10037584,
mondo:0006939,pyelonephritis,"['kidney infection', 'pyometrium']",11400,,,C0034186,,C34965,1001141,D011704,590.80,,10037596,
mondo:0006940,radial nerve lesion,"['lesion of radial nerve', 'radial nerve lesions', 'peripheral nerve lesion of radial nerve', 'radial nerve peripheral nerve lesion']",12170,,,C0154744,,,1001143,,354.3,,10061477,
mondo:0006941,rat-bite fever,"['Streptobacillosis', 'spirillosis', 'rat bite fever']",,,31205,C0034686,,C34971,1001144,D011906,026.9,,10037904,
mondo:0006944,renal aminoaciduria,,,,,,,,1001149,D000608,,,10001939,
mondo:0006945,renal artery obstruction,,2972,,,C0035066,,,1001150,D012078,,,,
mondo:0006946,renal osteodystrophy,"['osteodystrophy, renal', 'Osteodystrophies, renal', 'renal Osteodystrophies', 'renal rickets', 'rickets, renal']",13068,,,C0035086,,,1001152,D012080,588.0,N25.0,10038489,
mondo:0006947,renovascular hypertension,"['renovascular hypertension', 'renovascular hypertension (disease)']",1591,,,C0020545,,,1001153,,405.91,I15.0,,0100817
mondo:0006948,retinal artery occlusion,,8483,,,C0035302,,C34978,1001154,D015356,,,10038827,
mondo:0006949,retinal drusen,,2569,,,C0035312,,,1001155,D015593,362.57,,10062776,
mondo:0006950,retinal vasculitis,['retinal vasculitis'],11563,,,C0152026,,,1001156,D031300,362.18,,10038905,
mondo:0006951,retinal vein occlusion,"['occlusion, of retinal vein', 'retinal vein occlusion']",1727,,,C0035328,,C34981,1001157,D012170,,,10038907,
mondo:0006952,retinopathy of prematurity,"['retrolental fibroplasia', 'ROP', 'premature retinopathy', 'Terry syndrome']",13025,,90050,C0035344,,C34982,1001158,D012178,362.21,,10038933,
mondo:0006953,Rh isoimmunization,['Rh incompatibility affecting management of mother'],4175,,,C0035404,,,1001159,,,,10039016,
mondo:0006955,rheumatic heart disease,"['RHD', 'heart disease, rheumatic', 'disease, rheumatic heart', 'rheumatic carditis']",0050827,,,,,C34882,1001161,D012214,398.99,,10062110,
mondo:0006956,Rickettsiosis,"['infection, Rickettsia', 'Rickettsia caused disease or disorder', 'Rickettsial infectious disorder', 'Rickettsia infection', 'infections, Rickettsia', 'Rickettsial disease', 'Rickettsial infectious disease', 'Rickettsiosis', 'Rickettsiae disease']",,,102021,C0035585,,C34991,1001162,D012282,083.9,A75-A79,10061495,
mondo:0006957,root caries,"['root caries', 'dental caries of root surface', 'cementum caries', 'cementum dental caries', 'dental caries of cementum']",14089,,,C0162644,,,1001163,D017213,521.08,,,
mondo:0006960,sciatic neuropathy,,11446,,,C0149940,,,1001166,D020426,,,10048950,
mondo:0006961,scrapie,,5434,,,C0036457,,,1001168,D012608,,,,
mondo:0006962,sebaceous adenocarcinoma,"['carcinoma of sebaceous gland', 'sebaceous gland adenocarcinoma', 'malignant sebaceous tumour', 'sebaceous gland carcinoma', 'sebaceous carcinoma', 'Seba', 'adenocarcinoma of the sebaceous gland', 'carcinoma of the sebaceous gland', 'adenocarcinoma, sebaceous, malignant', 'sebaceous cancer', 'malignant sebaceous tumor']",4840,,,C1382026,,C8409,1001171,D018266,,,,
mondo:0006963,sebaceous gland neoplasm,"['sebaceous neoplasm', 'sebaceous tumor', 'sebaceous tumour', 'sebaceous gland tumor', 'sebaceous gland neoplasm (disease)', 'neoplasm of sebaceous gland', 'tumour of sebaceous gland', 'sebaceous gland tumour', 'sebaceous gland neoplasm', 'tumor of sebaceous gland']",5759,,,C3805742,,C3363,1001172,D012626,239.2,,,
mondo:0006964,secondary hyperparathyroidism,"['secondary hyperparathyroidism (disease)', 'secondary hyperparathyroidism NOS', 'secondary hyperparathyroidism']",12466,,,C0020503,,C113335,1001173,D006962,,,10020708,0000867
mondo:0006965,secondary hypertrophic osteoarthropathy,"['hypertrophic pulmonary osteoarthropathy (disorder) [ambiguous]', 'Bamberger-Marie disease', 'Marie Bamberger disease', 'HPOA - hypertrophic pulmonary osteoarthropathy', 'hypertrophic pulmonary osteoarthropathy']",10393,,,C0029412,,,1001174,D010005,731.2,,,
mondo:0006966,secondary Parkinson disease,"['symptomatic parkinsonism', 'secondary parkinsonism (disorder) [ambiguous]', 'secondary parkinsonism, unspecified', 'secondary Parkinsonism', 'disorder presenting primarily with parkinsonism']",13548,,,C0030569,,C34899,1001175,D010302,332.1,,,
mondo:0006968,shoulder impingement syndrome,"['subacromial impingement', 'shoulder impingement syndrome (disorder) [ambiguous]', 'Impingement syndrome of shoulder region']",14276,,,C0376685,,,1001178,D019534,726.2,M75.4,10049039,
mondo:0006969,sialadenitis,"['sialoadenitis', 'sialitis', 'saliva-secreting gland lymphadenitis (disease)', 'adenitis, salivary gland', 'salivary gland inflammation']",10303,,,C0037023,,C26882,1001179,D012793,527.2,,10040627,
mondo:0006970,sialolithiasis,"['Stone of salivary gland or duct', 'sialolith', 'salivary gland Stone']",12905,,,C0036091,,,1001180,D015494,527.5,K11.5,10040631,
mondo:0006971,sigmoid neoplasm,"['sigmoid colon tumor', 'sigmoid colon tumour', 'tumor of sigmoid colon', 'neoplasm of sigmoid colon', 'sigmoid colon neoplasm (disease)', 'tumour of sigmoid colon']",1896,,,C0037073,,,1001181,D012811,153.3,,10026456,
mondo:0006972,silo filler disease,"['silo-fillers^ disease', 'silo filler^s disease', 'silo filler disease']",4374,,,C0037120,,,1001182,D012832,,,,
mondo:0006973,skin appendage carcinoma,"['carcinoma of skin appendage', 'carcinoma, adnexal, malignant', 'cutaneous appendage carcinoma', 'adnexal carcinoma', 'carcinoma of cutaneous appendage', 'carcinoma of adnexa', 'skin appendage carcinoma', 'skin adnexal carcinoma']",,,,C0206697,,C3775,1001183,D018280,,,10040798,
mondo:0006974,small cell sarcoma,"['small cell sarcomas', 'small cell sarcoma']",3098,,,C0206652,,C3746,1001184,D018228,,,,
mondo:0006975,smooth muscle tumor,"['smooth muscle tumor', 'tumour of smooth muscle', 'tumour of the smooth muscle', 'smooth muscle neoplasm', 'tumor of smooth muscle', 'neoplasm of smooth muscle', 'neoplasm of the smooth muscle', 'tumor of the smooth muscle']",4310,,,C0206658,,C3751,1001185,D018235,,,,
mondo:0006976,somatostatinoma,"['Delta cell tumour', 'Delta cell tumor', 'somatostatin-secreting pancreatic neoplasm', 'somatostatinoma', 'tumour of the Delta cells', 'somatostatin cell tumor', 'Somatomedin-secreting carcinoid', 'somatostatin producing tumor', 'somatostatin producing tumour', 'somatostatin-producing neuroendocrine tumor', 'tumor of the Delta cells', 'somatostatin-producing tumour', 'somatostatin cell neoplasm', 'somatostatin-producing NET', 'malignant islet cell tumour', 'malignant islet cell tumor', 'ampullary somatostatinoma', 'tumour of Delta cells', 'somatostatin cell tumour', 'somatostatin-producing neuroendocrine tumour', 'carcinoid somatostatinoma', 'somatostatin-producing tumor', 'tumor of Delta cells']",4430,,97283,C0037661,,C3379,1001187,D013005,235.5,,10041329,
mondo:0006977,spermatocele,,11997,,,C0037859,,,1001189,D013088,608.1,N43.4,10041490,
mondo:0006978,splenic infarction,"['splenic infarction', 'infarct of the spleen', 'splenic infarcts', 'splenic infarct']",2533,,,C0037998,,,1001190,D013159,289.59,D73.5,10041648,
mondo:0006979,steatitis,"['Nutritional Panniculitis', 'Yellow fat disease', 'Nutritional Steatitis']",4025,,,C0038235,,,1001191,D013231,,,,
mondo:0006980,struma ovarii,"['struma ovarii', 'struma ovarii NOS (morphologic abnormality)', 'struma ovarii (morphologic abnormality)']",2640,,,C0038478,,C7468,1001192,D013330,,,,
mondo:0006981,subacute bacterial endocarditis,"['SBE', 'Subacute bacterial endocarditis', 'endocarditis lenta', 'SBE - Subacute bacterial endocarditis', 'Subacute endocarditis, lenta']",4562,,,C0014122,,C34583,1001193,D004698,,,10042271,
mondo:0006982,subacute thyroiditis,"['DeQuervain thyroiditis', 'granulomatous thyroiditis', 'De Quervain thyroiditis', 'de Quervain^s thyroiditis', 'Subacute thyroiditis', 'Subacute granulomatous thyroiditis', 'giant-cell thyroiditis', 'De Quervain^s thyroiditis']",7165,,,C0040149,,C35828,1001194,D013968,245.1,E06.1,10042298,
mondo:0006983,subclavian steal syndrome,"['subclavian artery stenosis', 'subclavian steal steno-occlusive disease', 'subclavian steal phenomenon']",13002,,,C0038531,,C35044,1001195,D013349,435.2,,10042335,
mondo:0006984,subdural empyema,['subdural abscess'],11389,,,C0038539,,,1001196,D013354,,,10042360,
mondo:0006986,substernal goiter,"['retrosternal thyroid goiter', 'retrosternal thyroid goitre']",13200,,,C0018024,,,1001198,D006045,,,,
mondo:0006987,subvalvular aortic stenosis,,5805,,,C0340375,,C85172,1001199,D001020,,,10042431,
mondo:0006988,sulfhemoglobinemia,['Sulfemoglobinemia'],12451,,,C0038732,,,1001200,D013436,,,10042481,
mondo:0006989,suppurative periapical periodontitis,"['apical abscess', 'periapical dental abscess', 'suppurative apical periodontitis', 'dentoalveolar abscess', 'periapical abscess']",2562,,,C0031024,,C34913,1001202,D010482,,,,
mondo:0006990,suppurative uveitis,,13140,,,C0042168,,,1001203,D015829,,,,
mondo:0006992,syphilitic aortitis,,,,,C0003511,,,1001206,,093.1,A52.02,10042900,
mondo:0006993,systolic heart failure,,9651,,,C1135191,,,1001207,D054143,428.20,,10074631,
mondo:0006994,tarsal tunnel syndrome,"['neuropathy of the posterior tibial nerve and its branches', 'posterior tibial nerve neuralgia']",12526,,,C0039319,,C85183,1001208,D013641,355.5,G57.5,10043121,
mondo:0006995,tethered spinal cord syndrome,"['spinal cord syndrome', 'tethered cord']",1089,,,,,C99080,1001210,D016135,756.19,,,
mondo:0006996,thyroid crisis,"['thyrotoxic crisis', 'thyroid storm', 'thyroid crisis (disease)', 'thyroid crisis']",12837,,,C0040127,,C112836,1001212,D013958,242.91,,10043705,0011782
mondo:0006997,tibial neuropathy,"['Posterior tibial neuropathy', 'tibial neuropathy (disorder) [ambiguous]']",1187,,,C0751932,,,1001213,D020429,,,,
mondo:0006998,tonsil cancer,"['malignant tumour of the tonsil', 'tonsil cancer', 'malignant neoplasm of tonsil', 'malignant neoplasm of palatine tonsil', 'malignant tonsil neoplasm', 'malignant neoplasm of tonsil, faucial', 'malignant tumor of the tonsil', 'malignant neoplasm of faucial tonsil', 'cancer of tonsil', 'malignant neoplasm of the tonsil', 'malignant tumour of tonsil', 'malignant tonsillar neoplasm', 'malignant tonsillar tumour', 'malignant tonsil tumour', 'malignant tonsillar tumor', 'malignant tumor of tonsil', 'malignant tonsil tumor']",8858,,,C0751560,,C7404,1001214,D014067,146.0,C09,10044002,
mondo:0006999,tooth disorder,"['tooth disorder', 'disease of calcareous tooth', 'calcareous tooth disease or disorder', 'disorder of calcareous tooth', 'dental disorder', 'calcareous tooth disease']",1091,,,C0040435,,C35077,1001216,D014076,,,,
mondo:0007000,Treponema infectious disease,"['Bejels', 'infections, Treponemal', 'Treponema caused disease or disorder', 'Treponemal infection', 'infection, Treponemal', 'bejel']",,,,,,C85197,1001217,D014211,,,,
mondo:0007001,tricuspid valve prolapse,"['tricuspid valve prolapse', 'tricuspid valve prolapse (disease)']",5644,,95458,C0040962,,,1001218,D014263,,,10066862,0001704
mondo:0007002,trochlear nerve disorder,"['IVth cranial nerve disorder', 'disease of trochlear nerve', 'trochlear nerve disease or disorder', 'trochlear nerve disorder', 'IVth nerve disorder', 'disorder of trochlear nerve', 'superior oblique muscle innervation disorder', 'trochlear nerve disease']",13864,,,,,C78395,1001220,D020432,378.53,,10074765,
mondo:0007004,type III hypersensitivity disease,"['immune complex disease', 'type III hypersensitivity reaction', 'disorder of type III hypersensitivity', 'type 3 hypersensitivity reaction', 'hypersensitivity reaction type III disease', 'type III hypersensitivity']",1557,,,C0020951,,C114346,1001222,D007105,,,10045265,
mondo:0007005,ulcerative proctosigmoiditis,,,,,,,,1001223,,556.3,,,
mondo:0007006,ulnar neuropathy,"['mononeuropathy of ulnar nerve', 'ulnar neuropathy (disorder) [ambiguous]', 'ulnar nerve mononeuropathy', 'ulnar neuropathy']",4613,,,C0154743,,,1001224,D020424,,,,
mondo:0007007,Ureaplasma urethritis,"['Ureaplasma infection', 'infection, Ureaplasma', 'Ureaplasma caused disease or disorder', 'infections, Ureaplasma']",,,,,,,1001225,D016869,,,,
mondo:0007008,uremia,['uremia of renal origin'],4676,,,C0041948,,,1001226,D014511,,,10046369,
mondo:0007009,ureterolithiasis,"['ureteric calculus', 'ureteric stone', 'calculus of ureter']",14146,,,C0041952,,C114696,1001228,D053039,592.1,,,
mondo:0007011,uveoparotid fever,"['uveoparotid fever', 'Heerfordt^s syndrome']",13404,,,C0042171,,,1001232,D014608,,,,
mondo:0007012,variant Creutzfeldt-Jakob disease,['vCJD'],5435,,576370,C0085209,,C26802,1001233,D016643,046.11,A81.01,10064199,
mondo:0007013,vasculogenic impotence,,4762,,,C0243000,,,1001234,D018783,,,,
mondo:0007014,vibrio infectious disease,['Vibrio caused disease or disorder'],,,,C0042636,,,1001235,D014735,,,,
mondo:0007015,viral meningitis,,10310,,,C0025297,,C118298,1001236,D008587,321.2,A87,10047469,
mondo:0007016,vitamin A deficiency,"['vitamin A deficiency', 'vitamin A deficiencies', 'deficiencies, vitamin A', 'vitamin A deficiency (disease)', 'deficiency, vitamin A']",,,,C0042842,,C85220,1001237,D014802,264.9,,10047586,0004905
mondo:0007017,vitreous detachment,"['vitreous, detachment Of', 'detachment Of vitreous']",9726,,,C0042907,,C50807,1001238,D020255,,,10047650,
mondo:0007018,vulvitis,['mammalian vulva inflammation'],3901,,,C0042996,,,1001239,D014847,,,10047780,
mondo:0007019,vulvovaginitis,['Vulvo-vaginitis'],2273,,,C0042998,,C35131,1001240,D014848,,,10047794,
mondo:0007020,Wernicke encephalopathy,"['Wernicke^s encephalopathy', 'dementia due to thiamine deficiency', 'Wernicke^s disease']",2384,,97354,C0043121,,,1001241,D014899,265.1,E51.2,,
mondo:0007022,xanthogranulomatous pyelonephritis,['xanthogranulomatous pyelonephritis'],11401,,,C0034188,,C123038,1001244,D011705,582.89,,10074389,
mondo:0007023,Yersinia infectious disease,"['infection, Yersinia', 'Yersinia infection', 'infections, Yersinia', 'infections, Yersinia <bacteria>', 'Yersinia <bacteria> infection']",,,,,,C128337,1001245,D015009,,,,
mondo:0007024,Yersinia pseudotuberculosis infectious disease,"['Pasteurella pseudotuberculosis', 'Pasteurella Pseudotuberculoses', 'infections, Yersinia pseudotuberculosis', 'Pseudotuberculoses, Pasteurella', 'pseudotuberculosis, Pasteurella']",,,,C0043410,,,1001246,D015012,,,,
mondo:0007025,chancre,,,,,,,,1001247,D002601,,,,
mondo:0007027,non-alcoholic steatohepatitis,"['nash - nonalcoholic Steatohepatitis', 'nonalcoholic Steatohepatitis']",0080547,,,,,C84445,1001249,,,,10053219,
mondo:0007028,rotator cuff syndrome,,,,,C0263912,,,1001250,,726.10,M75.1,,
mondo:0007029,branchio-oto-renal syndrome,"['Branchio oto renal syndrome', 'branchiootorenal dysplasia', 'Melnick-Fraser syndrome', 'bor syndrome', 'Branchio-Oto-renal syndrome', 'Branchio-otorenal dysplasia', 'branchiootorenal syndrome']",14702,,107,CN043574,"['0.342', '0.01162', '0.291', '-0.2493', '-0.00979', '-0.08044', '0.2181', '0.516', '-0.593', '-0.409', '0.1824', '-0.749', '-0.2097', '0.1895', '-0.5405', '-0.2837', '0.263', '-0.3525', '-0.2175', '-0.10156', '0.3218', '0.1536', '0.5225', '-0.08185', '0.3616', '-0.1362', '-0.541', '0.3076', '0.4915', '-0.04416', '0.5522', '-0.2874', '0.1619', '0.03232', '0.3955', '-0.713', '-0.007267', '-0.7373', '-0.1824', '-0.4468', '0.02736', '0.5054', '0.6357', '-0.0931', '-0.1127', '-0.5796', '-0.0604', '-0.57', '-0.1456', '0.1455', '-0.01727', '-0.04514', '0.2156', '-0.6353', '-0.352', '-0.4783', '0.2693', '0.10657', '-0.621', '-0.03592', '0.2493', '-0.2119', '-0.365', '0.3425', '-0.05896', '-0.1316', '0.2583', '0.3743', '-0.2048', '-0.126', '-0.306', '-0.372', '0.067', '-0.1799', '-0.0005417', '-0.2446', '0.582', '-0.12415', '-0.3284', '0.01912', '0.0663', '-0.07025', '0.1365', '1.021', '-0.531', '-0.01455', '0.1934', '0.434', '-0.01326', '0.1898', '-0.3274', '0.4094', '0.1357', '0.1044', '0.995', '-0.2795', '0.583', '-0.831', '-0.03452', '0.7314']",C98983,1001251,D019280,759.89,,10071135,
mondo:0007030,autosomal dominant Aarskog syndrome,"['Aarskog syndrome, autosomal dominant', 'faciogenital dysplasia', 'Aarskog-Scott syndrome', 'Aarskog syndrome']",0111825,100050,915,,"['-0.5117', '0.1317', '0.1792', '-0.4055', '0.1226', '-0.3074', '0.05704', '1.057', '-0.8184', '-0.8457', '0.619', '0.4565', '0.1239', '0.3167', '0.2544', '0.2625', '0.1171', '-0.2756', '-0.4395', '-0.6494', '-0.3467', '-0.1322', '0.727', '0.05676', '0.2937', '-0.3047', '-0.01157', '-0.0698', '0.5166', '-0.2563', '0.2627', '-0.7153', '-0.1582', '0.1508', '-0.0632', '-0.39', '0.1295', '0.0632', '-0.06042', '0.3064', '0.1304', '-0.2118', '0.251', '0.0594', '0.4993', '-0.313', '-0.0912', '0.3286', '-0.11414', '0.0922', '-0.3735', '-0.1087', '-0.868', '0.5864', '-0.4062', '0.0958', '0.012505', '-0.2285', '-0.06158', '0.709', '-0.045', '-0.00905', '-0.181', '0.2415', '0.3296', '0.2903', '-0.04538', '0.593', '-0.05154', '0.1375', '-0.4697', '0.6133', '0.02975', '0.437', '-0.09686', '0.347', '-0.04697', '0.01022', '-0.53', '-0.2041', '0.5347', '-0.06854', '0.0702', '0.3208', '0.1254', '0.3254', '-0.3225', '-0.403', '0.4329', '0.7017', '0.0904', '0.1874', '-0.285', '-0.1838', '0.578', '-0.5312', '0.54', '-0.782', '0.4724', '0.4636']",,,C535331,,,,
mondo:0007031,familial abdominal aortic aneurysm,"['aortic aneurysm, familial abdominal', 'hereditary abdominal aortic aneurysm']",,,86,CN206207,,,,,,,,
mondo:0007032,prune belly syndrome,"['Obrisnksy syndrome', 'eagle-Barrett syndrome', 'triad syndrome', 'PBS', 'syndrome of agenesis of abdominal muscles', 'abdominal muscles, absence of, with urinary tract Abnormality and cryptorchidism', 'prune belly syndrome', 'abdominal muscle deficiency syndrome', 'eagle-Barret syndrome', 'Obrinsky syndrome']",0060889,100100,2970,C0265363,"['-0.3828', '-0.903', '0.505', '-0.2084', '0.01677', '-0.5977', '0.02925', '0.972', '-0.264', '-0.0542', '-0.272', '-0.1442', '-0.1722', '-0.02678', '-0.4985', '-0.0329', '-0.5093', '0.0203', '-0.3281', '-0.857', '-0.4446', '-0.1696', '0.5215', '-0.4797', '0.1051', '-0.3792', '-0.0712', '0.4514', '0.5605', '-0.356', '0.4521', '-0.7124', '0.2974', '0.02504', '-0.4023', '-0.363', '-0.139', '0.3298', '0.2332', '-0.253', '-0.5405', '0.295', '0.2192', '-0.563', '0.4143', '0.11755', '-0.524', '-0.255', '-0.2617', '0.4814', '-0.583', '0.03223', '0.09406', '-0.799', '-0.7583', '0.2578', '0.1355', '-0.4526', '-0.1388', '0.02988', '0.1534', '0.283', '-0.2136', '0.4382', '-0.2278', '-0.1714', '0.4314', '-0.1332', '-0.195', '0.286', '-0.2241', '-0.03348', '0.3464', '0.157', '-0.2903', '-0.621', '0.532', '-0.07764', '-0.2583', '-0.762', '-0.2482', '-0.3242', '0.279', '0.6904', '-0.1719', '0.0917', '0.1958', '-0.3132', '0.1714', '-0.673', '-0.147', '0.02461', '-0.2223', '0.466', '0.6807', '-0.341', '0.4517', '-0.793', '0.407', '0.02806']",C85033,,D011535,756.71,,10051025,
mondo:0007033,abducens nerve palsy,"['6th nerve palsy', 'cranial mononeuropathy VI', 'sixth cranial nerve palsy', 'abducent nerve paralysis', 'lateral rectus muscle denervation paresis', 'VI nerve palsy', 'lateral rectus muscle innervation disorder', 'sixth nerve palsy', 'sixth cranial nerve disorder', 'cranial nerve VI palsy', 'abducens nerve weakness', 'abducens palsy', 'VIth nerve disorder', 'abducens nerve disease', 'cranial nerve palsy of abducens nerve', 'abducens nerve cranial nerve palsy', 'sixth nerve paralysis', 'disorder of abducent nerve', 'sixth or abducens nerve palsy', 'VIth nerve paralysis']",10865,100200,,,,C27592,,,378.54,,,
mondo:0007034,Adams-Oliver syndrome,"['limb scalp and skull defects', 'limb, scalp and skull defects', 'congenital scalp defects with distal limb anomalies', 'Adams Oliver syndrome', 'congenital scalp defects with distal limb reduction anomalies', 'AOS']",0060227,,974,C0265268,"['-0.317', '-0.188', '0.1346', '-0.5786', '0.1163', '-0.3435', '0.2438', '0.3606', '-0.7466', '-0.45', '-0.4739', '0.01897', '0.1469', '-0.2039', '-0.2065', '-0.2266', '0.1366', '-0.531', '-0.4468', '-0.9385', '-0.04242', '0.3904', '0.551', '-0.0801', '0.2024', '-0.546', '-0.414', '0.667', '0.6685', '0.2205', '0.3801', '-0.1147', '0.0794', '0.2067', '0.2113', '-0.4448', '-0.11395', '-0.275', '0.04895', '-0.1613', '0.0653', '-0.2423', '0.464', '0.01217', '0.658', '-0.6777', '-0.2281', '0.6', '0.2522', '-0.3254', '-0.4895', '0.1285', '0.3223', '-0.523', '-0.542', '-0.2834', '-0.2267', '-0.0925', '0.05173', '-0.0212', '-0.2817', '-0.2927', '0.079', '0.0538', '-0.502', '0.4053', '0.2362', '0.559', '-0.429', '0.2025', '-0.547', '-0.1992', '-0.428', '0.00443', '-0.1105', '-0.10956', '0.1807', '-0.4053', '-0.0312', '-0.7754', '0.3389', '0.1192', '0.1946', '0.6577', '0.02745', '-0.07654', '-0.04922', '0.1879', '-0.1597', '0.2307', '-0.1937', '0.12085', '0.38', '0.03006', '0.4211', '-0.5024', '0.657', '-0.2404', '0.32', '0.1897']",,,C538225,759.89,,,
mondo:0007035,acanthosis nigricans,"['an - acanthosis nigricans', 'keratosis nigricans', 'acanthosis nigricans (disease)', 'acanthosis nigricans']",3138,,924,C0000889,,C26687,1000660,D000052,,L83,,0000956
mondo:0007036,Achard syndrome,"['Achard syndrome', 'arachnodactyly, receding lower jaw and joint laxity of hands/feet']",6686,100700,,C1332135,,C35809,,C536012,,,,
mondo:0007037,Achondroplasia,"['Achondroplastic dwarfism', 'Achondroplasia', 'ACH', 'Achondroplastic physique', 'chondrodystrophia']",4480,100800,15,C0001080,"['0.3447', '0.624', '-0.1383', '-0.767', '-0.586', '-0.05554', '0.7173', '1.022', '-0.453', '-0.1697', '0.1344', '0.09717', '0.08887', '-0.012856', '0.00429', '-0.2563', '0.2742', '-0.119', '-0.395', '-0.3943', '-0.2625', '-0.1959', '0.72', '-0.0996', '-0.362', '-0.04666', '-0.2917', '-0.4282', '0.4478', '0.2059', '0.1896', '-0.2112', '0.4954', '-0.1517', '-0.2183', '-0.07104', '0.1329', '-0.588', '0.4722', '-0.1698', '-0.28', '0.1608', '0.466', '-0.01773', '0.0982', '0.323', '-0.329', '0.07477', '0.1818', '0.02985', '-0.01675', '0.3398', '0.3064', '-0.10706', '-0.2191', '-0.3308', '-0.3396', '-0.6973', '0.3508', '-0.0446', '0.05988', '0.797', '-0.7573', '0.6016', '-0.1984', '0.6606', '-0.145', '0.483', '-0.3796', '0.4155', '-0.04498', '0.1553', '-0.07825', '-1.005', '-0.428', '0.0661', '0.179', '-0.3696', '-0.7695', '-0.439', '-0.4668', '-0.3032', '0.0441', '0.6455', '0.1058', '0.9688', '-0.09534', '-0.00122', '0.703', '-0.1606', '-0.5146', '0.1884', '-0.702', '0.4639', '0.305', '-0.503', '0.75', '-0.1593', '0.4092', '0.1503']",C34345,,D000130,,Q77.4,10000452,
mondo:0007038,Achoo syndrome,"['Peroutka sneeze', 'autosomal dominant compelling helio ophthalmic outburst syndrome', 'autosomal dominant compelling Helioophthalmic outburst syndrome', 'Achoo syndrome', 'photic sneeze reflex', 'sneezing from Light exposure']",,100820,,C1863416,,,0007887,C535300,,,,
mondo:0007039,neurofibromatosis type 2,"['central neurofibromatosis', 'neurofibromatosis, type 2', 'neurofibromatosis, type II', 'neurofibromatosis, central type', 'bilateral acoustic neurofibromatosis', 'acoustic schwannomas bilateral', 'neurofibromatosis type 2', 'acoustic neurinoma bilateral', 'neurofibromatosis central type', 'NF2', 'acoustic neurofibromatosis', 'neurofibromatosis 2', 'acoustic neurinoma, bilateral', 'acoustic Schwannomas, bilateral', 'neurofibromatosis type II']",0111252,101000,637,C0027832,"['0.5044', '0.5156', '0.1091', '-0.583', '0.713', '0.1154', '0.0437', '0.8745', '-1.018', '-0.10956', '-0.1934', '-0.1426', '0.2915', '0.2502', '-0.2303', '-0.046', '0.3987', '0.113', '-0.3035', '0.09106', '-0.3174', '-0.4565', '0.2179', '0.3003', '-0.3142', '-0.3013', '-0.3672', '-0.5264', '0.1835', '0.2375', '0.7085', '-0.7256', '0.2108', '-0.1064', '-0.505', '0.002409', '-0.454', '0.3147', '0.2202', '0.10114', '0.441', '0.308', '0.1901', '-0.265', '0.51', '0.2228', '-0.4827', '-0.0313', '0.8877', '0.03815', '0.1082', '0.3743', '0.1426', '-0.2883', '0.498', '0.5317', '0.00543', '0.04367', '-0.2361', '0.04105', '-0.632', '-0.1504', '-0.36', '-0.1523', '0.04883', '0.938', '0.2666', '0.802', '-0.2542', '0.943', '0.1492', '0.1304', '0.0919', '-0.8623', '0.6885', '-0.2876', '-0.1316', '0.6143', '0.1619', '-0.3584', '-0.04208', '-0.0829', '0.444', '0.409', '-0.528', '-0.767', '0.4246', '0.504', '0.3062', '0.3354', '-0.721', '0.2805', '-0.551', '-0.718', '0.6494', '0.03842', '0.7896', '-0.1633', '0.3599', '0.5566']",C3274,,D009464,237.72,Q85.02,10029271,
mondo:0007040,Sakati-Nyhan syndrome,"['ACPS3', 'Sakati syndrome', 'ACPS with leg hypoplasia', 'ACPS 3', 'Sakati-Nyhan syndrome', 'acrocephalopolysyndactyly type III', 'Sakati-Nyhan-Tisdale syndrome', 'acrocephalopolysyndactyly type 3']",0060359,101120,3128,C1275079,,,,C537227,,,,
mondo:0007041,Apert syndrome,"['acrocephalosyndactyly type 1', 'Apert-Crouzon disease', 'ACS 2', 'ACS 1', 'ACS1', 'acrocephalosyndactyly, type 2', 'Apert syndrome', 'Vogt Cephalodactyly', 'syndactylic oxycephaly', 'type I Acrocephalosyndactyly', 'acrocephalosyndactyly, type 1', 'acrocephalo-syndactyly type 1', 'acrocephalosyndactyly type I']",,101200,87,C0001193,"['0.2466', '-0.6045', '0.1984', '-0.7505', '0.4465', '0.02266', '0.3977', '0.7783', '-0.9673', '-0.0842', '-0.3333', '-0.676', '-0.1428', '-0.09894', '-0.1459', '-0.3901', '0.3723', '-0.632', '-0.0699', '-0.9126', '-0.3274', '0.02287', '0.536', '-0.0826', '0.1506', '0.001203', '-0.2405', '0.2925', '0.352', '0.01825', '0.1376', '-0.012375', '-0.1727', '-0.148', '-0.0838', '-0.449', '0.1713', '-0.48', '0.05313', '-0.531', '0.1521', '-0.03482', '0.3875', '-0.1951', '0.7266', '-0.1333', '0.0791', '-0.3372', '0.421', '0.05664', '0.09924', '-0.08624', '0.10095', '-0.2242', '-0.4802', '0.0745', '-0.2834', '0.3848', '0.01746', '0.02423', '0.06445', '0.2651', '-0.2778', '0.2886', '0.01085', '0.02345', '-0.04266', '0.0385', '-0.8013', '0.2612', '-0.64', '0.4448', '0.3457', '-0.591', '0.348', '0.2362', '0.686', '-0.785', '-0.2983', '0.003576', '0.07245', '-0.4343', '-0.01371', '0.661', '-0.1825', '0.612', '-0.537', '0.2128', '-0.01392', '-0.0136', '-0.4521', '0.433', '0.01228', '0.1765', '0.09125', '0.02748', '0.7046', '-0.5957', '0.7896', '0.6367']",C99099,,D000168,,,10002943,
mondo:0007042,Saethre-Chotzen syndrome,"['Chotzen syndrome', 'Saethre-Chotzen syndrome with or without eyelid anomalies', 'SCS', 'ACS3', 'Saethre-Chotzen syndrome with eyelid anomalies', 'blepharophimosis, epicanthus inversus, and ptosis 3, formerly', 'acrocephalosyndactyly type III', 'blepharophimosis,epicanthus inversus, and ptosis 3 (formerly)', 'ACS 3', 'acrocephaly, skull asymmetry, and mild syndactyly', 'Saethre-Chotzen syndrome', 'acrocephalo-syndactyly, type 3', 'acrocephalosyndactyly, type 3', 'blepharophimosis, epicanthus inversus, and ptosis 3', 'type III Acrocephalosyndactyly', 'acrocephalosyndactyly type 3']",14768,101400,794,C0175699,"['0.6294', '0.12427', '-0.2241', '-0.541', '0.1167', '0.3545', '0.633', '0.8906', '-0.4548', '-0.004677', '-0.1571', '-0.399', '0.5205', '0.3828', '-0.483', '-0.2788', '0.367', '-0.4792', '-0.05713', '-0.6406', '0.0847', '-0.2161', '0.3657', '0.2108', '0.624', '-0.0893', '-0.2421', '0.361', '0.54', '0.2705', '0.289', '-0.0644', '0.519', '0.10333', '-0.6196', '0.2001', '0.1492', '-0.8354', '-0.2827', '-0.656', '0.11975', '-0.07367', '0.573', '-0.3303', '0.148', '-0.2374', '0.08496', '0.00811', '-0.2769', '0.3042', '0.3335', '0.2253', '-0.445', '-0.1813', '-0.11914', '-0.283', '0.01125', '-0.001045', '0.01775', '0.501', '0.644', '0.484', '0.11255', '0.3198', '-0.4814', '-0.205', '-0.12067', '0.5166', '-0.5015', '0.4395', '-0.2103', '0.633', '-0.1976', '-0.3953', '0.3064', '-0.2291', '0.1615', '-0.4695', '-0.4456', '-0.3386', '0.2703', '0.00363', '-0.4521', '0.9785', '-0.1721', '0.498', '-0.2463', '0.03793', '-0.1737', '-0.1854', '-0.513', '0.596', '-0.365', '0.76', '0.412', '-0.2468', '0.634', '-0.3818', '0.561', '0.434']",C75034,0007029,D000168,,,,
mondo:0007043,Pfeiffer syndrome,"['Pfeiffer syndrome', 'type V Acrocephalosyndactyly', 'ACS5', 'acrocephalosyndactyly type 5', 'acrocephalosyndactylia type V', 'acrocephalosyndactyly type V', 'Pfeiffer type acrocephalosyndactyly', 'acrocephalosyndactyly, type 5', 'Noack syndrome', 'ACS 5', 'craniofacial-skeletal-Dermatologic dysplasia']",14705,101600,710,C0220658,"['0.61', '-0.6094', '0.1394', '0.05725', '0.3564', '-0.2808', '0.4045', '0.43', '-1.119', '-0.2113', '-0.737', '-0.4287', '0.3228', '0.0904', '0.011894', '-0.264', '0.4553', '0.159', '0.0779', '-0.375', '-0.1145', '-0.136', '0.774', '0.05338', '0.396', '0.2517', '-0.2957', '0.3296', '0.5625', '0.0925', '0.482', '-0.0064', '0.4443', '0.2844', '-0.228', '0.03008', '-0.1818', '-0.1372', '0.1284', '-0.2472', '0.1066', '-0.10675', '0.616', '-0.2686', '0.718', '-0.3958', '-0.1445', '0.443', '-0.307', '0.2156', '0.02226', '-0.3267', '-0.07043', '-0.523', '0.1698', '0.02185', '-0.2294', '0.114', '0.0797', '-0.2266', '-0.12', '-0.0862', '0.1', '0.4321', '-0.2705', '0.0579', '-0.1816', '-0.275', '-0.6104', '0.5957', '-0.2274', '0.04782', '0.5767', '-0.255', '0.0981', '0.4539', '0.527', '-0.0236', '-0.5728', '-0.2096', '-0.08167', '-0.349', '0.2252', '0.879', '0.05695', '0.303', '0.1241', '0.324', '0.00997', '-0.1512', '-1.088', '0.1469', '0.1329', '-0.089', '0.1279', '0.3967', '0.7783', '-0.6416', '0.4097', '0.218']",C99100,,D000168,,,,
mondo:0007044,Acrodysostosis 1 with or without hormone resistance,"['Acrodysostosis 1 with or without hormone resistance', 'ADOHR', 'Acrodysostosis 1', 'Acrodysostosis 1, with or without hormone resistance', 'ACRDYS1']",,101800,,C3276228,,C136464,,,,,,
mondo:0007045,"acrofacial dysostosis, Catania type","['Opitz Mollica Sorge syndrome', 'acrofacial dysostosis Catania type', 'acrofacial dysostosis, Catania type', 'AFD Catania type', 'Afd, Catania type', 'Opitz-Caltabiano syndrome']",0060384,101805,1786,C2931762,,,,C538182,,,,
mondo:0007046,hereditary papulotranslucent acrokeratoderma,"['acrokeratoderma, hereditary papulotranslucent']",0060360,101840,,C1863343,,,1000708,C566323,,,,
mondo:0007047,punctate palmoplantar keratoderma type III,"['palmoplantar keratoderma, punctate type 3', 'near-total intestinal aganglionosis', 'ake', 'rare form of Hirschsprung^s disease', 'TIA', 'punctate palmoplantar keratoderma type 3', 'collagenous plaques of hands and feet', 'NTIA', 'punctate palmoplantar hyperkeratosis type 3', 'keratoderma, palmoplantar, punctate type 3', 'palmoplantar keratoderma, punctate type III', 'acrokeratoelastoidosis of Costa', 'PPKP3', 'collagenous plaques of hand and feet', 'acrokeratoelastoidosis', 'aganglionosis, total colonic']",0060362,101850,38,C0545044,,,1000758,C535653,,,,
mondo:0007048,acrokeratosis verruciformis,"['acrokeratosis verruciformis', 'AKV of Hopf', 'AKV', 'acrokeratosis verruciformis of Hopf', 'Hopf disease']",0050606,101900,79151,C0265971,"['-0.452', '0.3108', '0.2006', '-0.2289', '0.3655', '-0.563', '-0.2499', '-0.2438', '-0.517', '0.01851', '-0.10785', '0.11414', '-0.065', '-0.493', '-0.1804', '0.04688', '0.2274', '-0.498', '0.02711', '-0.6646', '-0.2465', '-0.271', '0.5835', '-0.0674', '0.138', '0.4905', '-0.3015', '0.1587', '0.03772', '-0.3364', '0.2532', '-0.4421', '-0.1464', '0.133', '0.4226', '-0.02126', '-0.4214', '0.2389', '0.4238', '-0.679', '0.00536', '-0.4412', '0.0637', '-0.1757', '0.4033', '-0.511', '-0.2069', '0.269', '0.10364', '-0.0777', '-0.1866', '0.2407', '0.1744', '-0.2374', '-0.6377', '-0.39', '0.391', '0.1705', '-0.5864', '-0.2688', '-0.007717', '-0.06934', '-0.424', '0.02417', '-0.01388', '0.09357', '0.426', '0.406', '0.2517', '0.7065', '-0.4539', '-0.269', '0.3909', '0.1414', '-0.2305', '0.065', '-0.2302', '0.013824', '-0.1126', '-0.6367', '-0.051', '-0.05692', '0.37', '0.1748', '0.0715', '-0.06903', '-0.3032', '0.447', '0.11194', '0.4614', '0.1809', '0.0794', '0.002037', '-0.02702', '0.319', '-0.1729', '0.4814', '-0.465', '0.1572', '0.144']",C27519,1000666,,757.39,,10069445,
mondo:0007049,"acroleukopathy, symmetric","['acroleukopathy, symmetric']",,102000,,C1863342,,,,C566322,,,,
mondo:0007050,"acromegaloid changes, cutis verticis gyrata, and corneal leukoma","['acromegaly-cutis verticis gyrata-corneal leukoma syndrome', 'Rosenthal-Kloepfer syndrome', 'acromegaloid changes, cutis verticis gyrata and corneal leukoma', 'acromegaloid changes, cutis verticis gyrata, and corneal leukoma']",,102100,964,CN225973,,,,C535654,,,,
mondo:0007051,acromegaloid facial appearance syndrome,"['thick lips and oral mucosa', 'acromegaloid facial appearance syndrome', 'AFA syndrome']",,102150,965,C0796280,,,,C535655,,,,
mondo:0007052,growth hormone secreting pituitary adenoma 1,"['PITA1', 'somatotropinoma, familial isolated', 'familial isolated pituitary adenoma syndrome', 'pituitary adenoma predisposition', 'pituitary adenoma 1, multiple types, autosomal dominant, somatic mutation', 'isolated familial somatotropinoma', 'pituitary adenoma, familial isolated', 'pituitary adenoma, growth hormone-secreting, 1', 'pituitary adenoma predisposition, autosomal dominant, somatic mutation', 'pituitary adenoma, growth hormone-secreting, type 1', 'acromegaly due to pituitary adenoma 1', 'Somatotrophinoma, familial', 'pituitary adenoma 1, multiple types', 'PAGH1']",0112009,102200,99725,,"['-0.0635', '0.06665', '0.0082', '-0.03857', '0.0295', '-0.0272', '0.01504', '0.09937', '-0.0727', '-0.0509', '-0.0216', '-0.004406', '0.02138', '0.0215', '-0.04138', '-0.0619', '-0.00227', '-0.0371', '-0.03918', '-0.1201', '-0.01404', '-0.0455', '0.04404', '-0.0491', '0.0313', '-0.0401', '-0.015396', '-0.02975', '-0.003815', '-0.04034', '0.087', '-0.01381', '0.07776', '-0.01277', '0.00311', '-0.0208', '-0.001434', '-0.01331', '-0.02931', '-0.03009', '0.0399', '-0.046', '0.0199', '-0.0409', '0.02908', '-0.07446', '0.004635', '0.04462', '0.02606', '0.03418', '-0.01459', '-0.02338', '-0.0088', '0.034', '-0.0718', '0.003395', '0.0644', '-0.05716', '-0.08075', '0.02617', '0.04962', '0.0377', '0.002506', '0.003792', '-0.012665', '0.03265', '0.0793', '0.07495', '-0.081', '0.05997', '-0.04343', '0.0248', '0.03976', '-0.05792', '0.02312', '0.03574', '0.00889', '-0.001072', '-0.0524', '-0.06665', '-0.01092', '0.02426', '-0.027', '0.02287', '-0.04816', '0.007046', '0.05804', '0.03043', '0.1132', '0.01326', '0.02179', '0.05313', '0.000707', '-0.0226', '0.1606', '0.01343', '0.0443', '-0.0886', '-0.01421', '0.0684']",,,,,,,
mondo:0007053,"restless legs syndrome, susceptibility to, 1","['RLS1', 'restless legs syndrome, susceptibility to, 1', 'acromelalgia, hereditary', 'Ekbom syndrome']",,102300,,C3888109,,,,C538443,,,,
mondo:0007054,acromial dimples,"['acromial dimples', 'supraspinous fossae, congenital']",,102350,,C1863321,,,,,,,,
mondo:0007055,Acromicric dysplasia,"['Acromicric skeletal dysplasia', 'ACMICD', 'Acromicric dysplasia']",0111243,102370,969,,"['-0.0435', '-0.3538', '0.3354', '-0.0542', '0.0439', '-0.5464', '0.534', '1.382', '-0.3047', '-1.035', '0.239', '0.084', '-0.01044', '0.4473', '-0.358', '0.3276', '0.4978', '-0.756', '-0.3794', '-0.4539', '-0.1871', '0.0242', '0.6367', '0.1605', '-0.264', '-0.1874', '-0.299', '-0.1355', '0.2058', '0.3914', '0.0775', '-0.4768', '0.2622', '-0.3032', '-0.341', '-0.2036', '-0.2612', '-0.4429', '0.3723', '-0.2162', '0.1543', '-0.2773', '0.3105', '0.2766', '0.8535', '-0.07263', '-0.05316', '0.454', '-0.1603', '-0.4558', '-0.464', '0.2428', '-0.3354', '0.268', '-0.1224', '-0.3057', '-0.4277', '-0.5117', '0.5386', '-0.139', '0.4033', '0.14', '-0.504', '0.1323', '-0.0826', '-0.2827', '-0.0418', '0.1725', '-0.3271', '0.4456', '-0.3757', '0.1422', '0.1547', '0.1423', '-0.2832', '0.07605', '0.1312', '0.06604', '-0.11914', '-0.1255', '0.2605', '-0.1313', '-0.559', '0.3594', '-0.5835', '0.3032', '-0.1448', '-0.04974', '0.9663', '0.319', '0.2172', '-0.1567', '-0.3767', '0.03592', '0.6904', '0.2761', '0.02469', '-0.655', '0.6343', '0.2097']",,,C535662,756.59,,,
mondo:0007056,acroosteolysis,['acroosteolysis'],,102400,,,,C35545,,D030981,,,,
mondo:0007057,Acroosteolysis dominant type,"['Hajdu-Cheney syndrome', 'acrodentoosteodysplasia', 'serpentine fibula-polycystic kidneys syndrome', 'Arthrodentoosteodysplasia', 'HJCYS', 'serpentine fibula polycystic kidney syndrome', 'acroosteolysis with osteoporosis and changes in skull and mandible', 'serpentine fibula-polycystic kidney syndrome', 'Cheney syndrome']",2736,102500,955,C2930971,"['0.317', '0.1514', '0.10535', '-0.2095', '-0.0925', '-0.1465', '0.2766', '0.752', '-0.304', '0.205', '-0.1489', '-0.4192', '-0.3076', '0.3352', '0.06555', '0.3088', '0.1092', '-0.4995', '-0.1543', '-0.522', '0.04446', '-0.04462', '0.442', '-0.2308', '0.4448', '-0.06744', '0.2053', '0.06805', '0.1431', '-0.5728', '0.7964', '-0.1575', '-0.2246', '0.1748', '0.1908', '-0.4329', '-0.1344', '-0.2126', '-0.4487', '-0.3774', '0.1895', '0.2401', '0.4854', '-0.1339', '0.1704', '-0.802', '0.02267', '0.3938', '-0.3577', '-0.1011', '0.1508', '0.2356', '0.5015', '0.2146', '-0.05133', '-0.853', '-0.512', '-0.186', '0.508', '0.2389', '0.1897', '-0.03735', '-0.4587', '-0.3064', '-0.4973', '0.1527', '0.622', '0.832', '0.11066', '0.7925', '0.00941', '-0.3936', '0.1987', '-0.2235', '-0.1407', '-0.332', '0.2217', '0.3176', '0.1113', '0.2097', '-0.464', '0.1693', '0.0434', '0.602', '0.02771', '0.078', '-0.3557', '0.431', '0.1338', '0.0471', '-0.1092', '0.4153', '-0.4585', '0.02417', '0.769', '-0.1593', '0.8813', '-0.1942', '0.0898', '0.369']",C84745,,C537586,756.59,,,
mondo:0007058,Acropectorovertebral dysplasia,"['Acropectorovertebral dysplasia', 'Acropectorovertebral dysplasia F form', 'ACRPV', 'F syndrome']",,102510,957,C1863307,,,,C566319,,,,
mondo:0007059,acrorenal syndrome,['acrorenal syndrome'],0060347,102520,971,CN206860,,,,C563159,,,,
mondo:0007060,spermatogenic failure 6,"['SPGF6', 'acrosome malformation of spermatozoa', 'globozoospermia', 'round-headed spermatozoa', 'azoospermia caused by mutation in SPATA16', 'spermatogenic failure type 6', 'spermatogenic failure 6', 'SPATA16 azoospermia', 'spermatozoa, round-headed']",0070167,102530,,,,,,,,,,
mondo:0007062,"adactylia, unilateral","['digits 2-5 hypodactyly, unilateral', 'digits 2-5 oligodactyly, unilateral', 'terminal transverse defects of hand, unilateral', 'Adactyly of hand, unilateral', 'adactylia, unilateral', 'congenital absence/hypoplasia of fingers excluding thumb, unilateral', 'adactylia unilateral']",,102650,973,,,,,C562417,,,,
mondo:0007064,"severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency","['adenosine deaminase deficiency, partial, Autosomal recessive, Somatic mosaicism', 'adenosine deaminase deficiency', 'SCID due to ADA deficiency, early-onset', 'SCID due to ADA deficiency', 'ADA', 'ADA deficiency', 'adenosine deaminase deficiency, partial', 'severe combined immunodeficiency due to ADA deficiency, Autosomal recessive, Somatic mosaicism', 'SCID due to adenosine deaminase deficiency', 'partial ADA deficiency', 'SCID due to ADA deficiency, delayed onset', 'SCID due to ADA deficiency, late-onset', 'severe combined immunodeficiency due to ADA deficiency', 'ADA-SCID', 'adenosine deaminase deficient severe combined immunodeficiency', 'severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, NK cell-negative, due to adenosine deaminase deficiency', 'severe combined immunodeficiency due to adenosine deaminase deficiency']",5810,102700,277,,"['0.014854', '0.277', '-0.04395', '-0.1078', '0.5464', '-0.04163', '0.649', '0.5547', '-0.443', '-0.3076', '-0.2275', '0.1671', '-0.3984', '0.1868', '-0.1838', '-0.6353', '0.2229', '-0.152', '-0.5776', '-0.459', '-0.2683', '-0.5615', '0.557', '-0.5913', '0.4482', '0.2966', '-0.02405', '-0.04303', '-0.2449', '-0.3682', '0.5205', '0.4458', '0.6523', '-0.06158', '-0.1841', '-0.2487', '-0.6494', '-0.3396', '-0.559', '0.2695', '-0.3364', '-0.3496', '0.4507', '-0.03876', '-0.3916', '-0.10693', '-0.1093', '-0.93', '-0.196', '0.48', '0.624', '-0.02292', '0.03268', '0.1964', '-0.02376', '-0.11725', '0.2401', '-0.2805', '-0.1737', '0.6313', '-0.0105', '0.07983', '0.5005', '0.647', '0.4888', '-0.359', '0.281', '-0.1378', '-0.137', '0.2546', '0.2148', '-0.1918', '-0.2627', '-0.10425', '0.4805', '-0.08655', '0.612', '-0.2727', '-0.1667', '-0.2822', '0.32', '-0.2495', '-0.02635', '0.3252', '-0.02188', '0.04916', '0.5747', '0.3215', '0.4824', '0.2866', '0.2512', '0.5107', '-0.4678', '-0.613', '0.6577', '1.175', '0.4333', '-0.676', '0.3071', '-0.366']",C3962,0009147,C531816,277.2,,10066367,
mondo:0007066,"adenosine triphosphatase deficiency, anemia due to","['anaemia due to adenosine triphosphatase deficiency', 'adenosine triphosphatase deficiency, anemia due to', 'anemia due to adenosine triphosphatase deficiency', 'adenosine triphosphatase deficiency anemia', 'adenosine triphosphatase deficiency anaemia']",,102800,1044,C1863225,,,,C566311,,,,
mondo:0007067,pyruvate kinase hyperactivity,"['pyruvate kinase hyperactivity', 'adenosine triphosphate, elevated, of erythrocytes']",,102900,,C1863224,"['-0.2927', '0.1145', '0.0692', '-0.0791', '-0.001075', '-0.1464', '-0.07056', '0.1847', '0.0004783', '-0.1481', '-0.07965', '0.0367', '0.108', '-0.05124', '0.00401', '-0.03018', '-0.03026', '-0.05692', '-0.04672', '-0.2512', '-0.10175', '-0.06476', '0.0731', '0.0356', '0.119', '0.01291', '-0.01804', '-0.1321', '-0.11774', '-0.1895', '0.1067', '0.0794', '0.291', '0.07', '-0.1687', '-0.10626', '-0.00247', '-0.0476', '0.012665', '-0.25', '0.03836', '-0.2249', '0.0738', '-0.08057', '-0.06647', '-0.317', '-0.002996', '0.12024', '0.11835', '0.01071', '0.05167', '-0.05597', '0.08594', '0.00945', '0.03784', '-0.09937', '0.1849', '-0.06494', '-0.1664', '0.0781', '0.03204', '0.005096', '0.1487', '-0.0886', '0.0894', '-0.012505', '0.1447', '0.1405', '-0.1665', '0.2632', '-0.04346', '-0.01276', '-0.0522', '0.02814', '0.1588', '0.101', '0.02008', '-0.05988', '-0.0532', '-0.11426', '0.03244', '0.001704', '-0.01598', '0.05746', '0.1028', '0.09656', '0.04276', '0.0707', '0.2686', '-0.001276', '0.1431', '0.201', '0.01089', '-0.11456', '0.3345', '0.3186', '0.10504', '-0.2361', '0.03226', '0.08276']",,0005840,C566310,,,,
mondo:0007068,adenylosuccinate lyase deficiency,"['ADSL deficiency', 'adenylosuccinase lyase deficiency', 'adenylosuccinase deficiency', 'Adsl deficiency', 'ADSLD', 'rare inborn error of (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate AMP-lyase (fumarate-forming) activity', 'adenylosuccinate lyase deficiency', 'inborn error of (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido)succinate AMP-lyase (fumarate-forming) activity']",0050762,103050,46,C0268126,"['0.0416', '0.343', '0.04602', '-0.1508', '0.1353', '-0.7754', '0.6333', '0.4329', '-0.4905', '-0.03967', '-0.6157', '-0.05145', '0.2345', '0.000366', '-0.1511', '0.2261', '0.1334', '-0.0939', '-0.2356', '-0.702', '-0.2255', '0.2573', '0.698', '-0.412', '0.177', '-0.2206', '0.1903', '-0.01895', '-0.4976', '-0.1765', '-0.0485', '-0.0994', '0.231', '0.6997', '-0.0979', '-0.3745', '-0.358', '-0.5347', '-0.2302', '-0.1482', '0.02641', '-0.4773', '-0.2263', '-0.07324', '0.4775', '-0.1776', '0.3271', '0.00513', '-0.54', '0.436', '-0.2656', '-0.2502', '-0.0242', '-0.2115', '0.144', '0.3098', '0.4033', '-0.279', '0.1764', '0.00708', '-0.6636', '-0.2225', '0.4749', '0.1427', '-0.268', '0.00046', '0.037', '-0.06384', '-0.3757', '-0.0948', '0.2156', '0.535', '-0.4856', '0.3003', '0.3608', '0.5024', '0.4097', '-0.812', '-0.2223', '0.2776', '0.2446', '0.3018', '-0.6543', '0.3196', '0.344', '0.14', '0.1157', '0.079', '0.7363', '0.474', '0.2494', '-0.02733', '-0.4602', '0.0965', '0.6074', '0.3928', '0.11945', '0.1095', '0.4849', '-0.046']",,,C538235,277.2,,,
mondo:0007070,adiposis dolorosa,"['lipomatosis dolorosa', 'adiposis dolorosa', 'Dercum^s disease', 'Neurolipomatosis', 'Adiposalgia', 'Dercum disease', 'adipose tissue rheumatism']",3928,103200,36397,C0001529,,C84540,1000667,D000274,272.8,,10001294,
mondo:0007071,"adrenocortical hypofunction, chronic primary congenital","['adrenocortical hypofunction, chronic primary congenital', 'Addison disease, congenital']",,103230,85138,C0271740,,,,C562711,255.41,,,
mondo:0007072,ADULT syndrome,"['acro dermato ungual lacrimal tooth syndrome', 'pigment anomaly-ectrodactyly-hypodontia syndrome', 'acrodermatounguallacrimaltooth syndrome', 'acro-dermato-ungual-lacrimal-tooth syndrome', 'ADULT syndrome', 'acro-dermato-ungual-lacrimal-Tooth syndrome']",0050601,103285,978,C1863204,"['0.10144', '-0.1154', '0.3757', '-0.4124', '0.5557', '-0.261', '0.1008', '0.2925', '0.2917', '-0.4966', '-0.46', '-0.1575', '-0.3738', '0.312', '-0.1495', '0.1948', '0.2404', '-0.2683', '-0.4263', '-0.4333', '-0.401', '-0.2281', '0.1032', '-0.4148', '0.2947', '0.1101', '-0.3425', '-0.1658', '0.7773', '-0.486', '0.428', '-0.1294', '-0.1087', '0.4119', '0.5', '-0.2291', '-0.267', '-0.2642', '-0.009895', '-0.03165', '0.251', '-0.314', '0.02843', '-0.4915', '0.2646', '-0.755', '0.147', '0.1376', '-0.28', '-0.2113', '0.1353', '0.4443', '-0.248', '0.2299', '-0.2793', '-0.4128', '0.1628', '-0.2289', '-0.6035', '-0.3892', '0.445', '0.1708', '-0.3557', '-0.1726', '0.2239', '-0.02434', '0.5806', '0.2993', '-0.08093', '0.2028', '-0.6665', '0.07416', '0.2546', '-0.2766', '0.3093', '-0.1694', '0.1936', '0.12286', '-0.02182', '-0.07733', '0.1837', '0.365', '0.1462', '0.3936', '0.06555', '-0.251', '0.0697', '0.292', '0.1443', '-0.3555', '0.1326', '0.653', '0.3582', '0.0814', '0.9365', '-0.442', '0.3582', '-0.4697', '0.2039', '0.612']",,,C538052,,,,
mondo:0007073,Hypoglossia-hypodactyly syndrome,"['aglossia-adactylia', 'peromelia with micrognathia', 'peromelia with micrognathism', 'oromandibular limb hypoplasia', 'aglossia-adactylia syndrome', 'aglossia adactylia', 'Jussieu syndrome', 'Hypoglossia-hypodactylia', 'Hypoglossia-hypodactylia syndrome', 'Hanhart syndrome']",,103300,989,,,,,,759.89,,,
mondo:0007074,ainhum,"['ainhum', 'ainhum (disease)', 'Dactylolysis', 'spontaneous dactylolysis', 'Dactylolysis spontanea']",11329,103400,,C0001860,,C84544,,D000387,136.0,L94.6,,0031009
mondo:0007075,"alacrima, congenital, autosomal dominant","['alacrimia congenita, autosomal dominant', 'alacrimia congenita', 'alacrima, congenital']",,103420,,,,,,C566307,,,,
mondo:0007077,Tietz syndrome,"['Tietz albinism-deafness syndrome', 'albinism-deafness of Tietz', 'Tietz syndrome', 'hypopigmentation/deafness of Tietz', 'TADS', 'hypopigmentation-deafness syndrome']",0090002,103500,42665,C0391816,"['0.13', '0.03824', '0.1534', '0.1606', '0.506', '-0.4663', '-0.3127', '0.742', '0.06555', '0.003355', '-0.0698', '-0.1544', '-0.33', '-0.1534', '-0.09766', '0.2925', '0.689', '0.001346', '0.10315', '-0.1559', '-0.1428', '-0.151', '0.01029', '-0.1274', '0.10956', '0.05185', '-0.623', '0.006363', '0.1516', '0.1121', '0.413', '-0.2198', '0.2942', '-0.0653', '-0.215', '-0.10474', '-0.3303', '-0.2708', '-0.127', '-0.2036', '0.3474', '-0.2089', '-0.1821', '-0.3926', '-0.314', '-0.5005', '0.0512', '0.11145', '0.1653', '-0.07904', '-0.10724', '-0.1481', '0.225', '0.1274', '-0.1367', '0.1403', '0.3958', '-0.2136', '-0.12103', '-0.314', '-0.1459', '-0.2717', '-0.1212', '0.06885', '-0.497', '-0.1516', '0.268', '0.666', '-0.0721', '0.6196', '-0.29', '0.1792', '0.1254', '-0.404', '0.03693', '-0.2488', '0.03476', '-0.0936', '-0.1102', '-0.0518', '0.4185', '-0.208', '0.2201', '0.4077', '-0.2478', '-0.502', '-0.01307', '0.6743', '0.2423', '0.6094', '0.4792', '0.8384', '0.1705', '0.4832', '0.5947', '-0.1338', '-0.04495', '-0.621', '0.536', '0.1807']",,,C536919,270.2,,,
mondo:0007078,Pseudohypoparathyroidism type 1A,"['Pseudohypoparathyroidism type 1A', 'Pseudohypoparathyroidism Ia', 'Pseudohypoparathyroidism, type 1A', 'Albright hereditary osteodystrophy with multiple hormone resistance', 'AHO', 'Pseudohypoparathyroidism, type IA', 'AHO-PHP syndrome Ia', 'Albright hereditary osteodystrophy', 'PHP 1A', 'Albright^s hereditary osteodystrophy', 'Albright hereditary osteodystrophy-PHP syndrome Ia', 'PHP1A']",0080053,103580,79443,C3494506,"['-0.05478', '-0.1313', '-0.0978', '0.03418', '-0.2842', '0.5215', '-0.02692', '0.7954', '-0.935', '-1.073', '-0.1802', '-0.1589', '-0.3958', '0.714', '-0.442', '0.5117', '-0.2705', '-0.596', '-0.0704', '-0.6523', '0.1858', '-0.1168', '0.457', '-0.4246', '0.2067', '0.0445', '-0.2708', '-0.3096', '0.4775', '-1.134', '0.1868', '0.1057', '0.02408', '0.3132', '-0.3574', '-0.6646', '0.05197', '-0.0627', '0.271', '0.3972', '0.47', '-0.02702', '0.6045', '-0.552', '0.5464', '-0.3936', '0.768', '0.466', '0.04642', '0.448', '0.1885', '0.3274', '0.6943', '-0.2057', '-0.8833', '-0.4165', '-0.1309', '-0.7515', '-0.4023', '-0.3796', '-0.1959', '-0.3206', '0.2089', '-0.2133', '-0.379', '0.669', '0.4724', '0.9453', '-0.5283', '0.1802', '-0.03616', '-0.2097', '0.3687', '-0.1465', '0.633', '0.1174', '0.081', '0.1177', '0.1665', '0.6055', '0.6567', '0.253', '-0.11536', '-1.072', '0.2267', '-0.298', '-0.04697', '0.2908', '0.6074', '0.2715', '0.04514', '0.7847', '-0.5156', '-0.2198', '0.3152', '-0.0673', '0.0475', '-0.37', '0.2144', '0.3796']",C129721,,C537045,275.49,,,
mondo:0007079,alcohol dependence,"['alcohol dependence, protection against', 'alcohol dependence, susceptibility to', 'aerodigestive tract cancer, squamous cell, alcohol-related, protection against', 'alcohol dependence', 'alcoholism']",0050741,103780,,,"['0.06226', '0.06696', '0.1616', '0.0643', '-0.10175', '-0.2556', '0.3389', '0.0904', '-0.1578', '-0.115', '-0.04596', '0.01404', '0.2786', '0.2133', '0.2094', '-0.1793', '-0.015', '0.1033', '-0.2903', '-0.4023', '-0.2427', '0.07086', '0.0987', '-0.1185', '0.102', '-0.1256', '0.02937', '-0.0825', '-0.2476', '-0.2214', '0.0661', '0.05673', '0.1903', '0.05655', '-0.03766', '-0.322', '0.06094', '-0.1686', '0.0707', '-0.2556', '0.1561', '-0.1537', '-0.0788', '0.03293', '0.1305', '-0.2385', '0.12213', '-0.03412', '0.12274', '0.2815', '-0.2979', '0.1326', '0.11926', '0.02855', '0.2383', '0.1198', '0.2158', '0.1823', '-0.222', '-0.2155', '0.09296', '0.2295', '0.0895', '0.05466', '-0.03497', '0.2788', '-0.0684', '0.1821', '-0.1991', '0.11395', '-0.01121', '0.0271', '0.12445', '-0.2034', '0.1273', '0.1057', '0.004555', '-0.04172', '-0.1354', '-0.22', '-0.02441', '-0.1056', '-0.0544', '0.3286', '0.02254', '0.07764', '0.01605', '0.009514', '0.3708', '0.02098', '0.03717', '0.11865', '-0.10913', '0.1182', '0.2031', '0.06726', '0.2395', '-0.1025', '-0.1162', '0.0887']",C93040,0003829,D019973,305.0,,,
mondo:0007080,glucocorticoid-remediable aldosteronism,"['ACTH-dependent hyperaldosteronism syndrome', 'aldosteronism, glucocorticoid-remediable', 'glucocorticoid sensitive hypertension', 'hyperaldosteronism, familial type 1', 'HALD1', 'GRA', 'hyperaldosteronism, familial, type I', 'dexamethasone sensitive hypertension', 'FH1', 'glucocorticoid-sensitive hypertension', 'aldosteronism, sensitive to dexamethasone', 'FH 1', 'dexamethasone-sensitive hypertension', 'hyperaldosteronism, familial, type 1', 'familial hyperaldosteronism type I', 'FH-I', 'familial hyperaldosteronism type 1', 'glucocorticoid-suppressible hyperaldosteronism', 'glucocorticoid-remediable aldosteronism']",14080,103900,403,C3838731,"['-0.4043', '-0.02718', '-0.1322', '-0.1161', '0.09863', '0.2195', '0.613', '0.572', '-0.5234', '0.0251', '-0.1416', '-0.01267', '0.4673', '0.1577', '-0.2737', '-0.4631', '-0.3909', '0.1624', '0.10974', '-0.8193', '-0.08105', '-0.287', '0.77', '-0.1147', '-0.014206', '0.1454', '0.3113', '0.01062', '0.0836', '0.1486', '0.6016', '-0.0955', '0.7617', '0.1721', '-0.51', '-0.03253', '-0.257', '0.1145', '0.2634', '-0.1439', '0.1978', '-0.3994', '0.4917', '-0.942', '0.1326', '-0.1241', '0.2133', '-0.1741', '0.04126', '0.6113', '0.1276', '0.507', '0.1758', '-0.8154', '-0.2664', '0.3643', '0.1664', '-1.138', '-0.4866', '0.3948', '-0.4521', '0.2903', '0.2083', '-0.9663', '-0.297', '0.2048', '-0.1449', '0.1974', '0.0538', '-0.284', '0.0794', '-0.02895', '0.1952', '-0.4858', '0.497', '0.4219', '-0.2075', '-0.294', '-0.136', '-0.3633', '-0.468', '0.6997', '-0.06885', '-0.2605', '0.3794', '-0.4307', '0.1259', '-0.09534', '0.2698', '-0.2874', '-0.3777', '-0.0914', '0.2145', '-0.4678', '0.939', '0.3372', '0.789', '-0.343', '-0.803', '0.01014']",,,C563177,255.11,E26.02,,
mondo:0007082,alopecia areata 1,"['AA1', 'alopecia universalis', 'alopecia areata 1']",,104000,701,C1863094,"['-0.1835', '0.1375', '0.2107', '-0.1171', '0.5933', '-0.3235', '-0.11145', '-0.156', '-0.2688', '0.02435', '-0.1884', '0.0671', '-0.1783', '-0.001161', '-0.4048', '-0.2551', '0.3323', '0.02293', '-0.2925', '-0.672', '-0.4243', '-0.1493', '0.3655', '-0.311', '0.3108', '0.2131', '-0.1815', '-0.08136', '-0.04028', '0.1312', '0.4111', '0.00813', '-0.01636', '0.0656', '0.4285', '0.2026', '-0.529', '0.1345', '-0.0646', '0.03665', '-0.12067', '-0.171', '0.1136', '-0.1881', '-0.159', '-0.3398', '-0.02173', '-0.1677', '0.3274', '0.06174', '-0.03117', '0.1534', '0.5967', '0.07996', '-0.5522', '-0.2876', '0.402', '-0.2976', '-0.416', '-0.5864', '-0.1097', '-0.05182', '0.2874', '-0.00736', '0.1703', '0.3135', '0.2915', '0.1951', '0.04352', '0.2727', '-0.1058', '-0.2499', '-0.0474', '-0.2163', '-0.1849', '0.3171', '0.03427', '0.04404', '-0.263', '-0.2678', '0.146', '-0.402', '0.1859', '0.11566', '0.1306', '-0.5435', '-0.1587', '0.5215', '0.1906', '0.573', '0.2362', '0.341', '0.2139', '0.3564', '0.5093', '0.1472', '0.1261', '-0.6113', '0.3489', '0.1658']",,,C566303,,,,
mondo:0007083,autosomal dominant palmoplantar keratoderma and congenital alopecia,"['palmoplantar keratoderma with congenital alopecia', 'autosomal dominant palmoplantar hyperkeratosis and congenital alopecia', 'palmoplantar keratoderma and congenital alopecia type 1', 'alopecia congenita with hyperkeratosis of the palms and soles', 'keratoderma-hypotrichosis-leukonychia totalis syndrome', 'PPKCA1', 'Ppkca, Stevanovic type', 'palmoplantar keratoderma and congenital alopecia 1', 'palmoplantar keratoderma and congenital alopecia, Stevanovic type', 'PPK-CA, Stevanovic type']",0111244,104100,1010,,"['-0.00886', '0.1034', '-0.3047', '-0.04773', '0.352', '-0.5923', '0.04715', '0.3525', '-0.2556', '-0.1631', '-0.196', '0.1976', '-0.4248', '0.09906', '-0.2032', '0.45', '0.4727', '-0.4253', '-0.4353', '-1.468', '-0.774', '0.3708', '0.2002', '-0.2556', '0.2239', '0.63', '-0.3335', '0.4583', '-0.189', '-0.2301', '0.581', '-0.1438', '0.0398', '0.000979', '-0.2922', '0.8535', '-0.586', '-0.2003', '-0.5215', '0.006435', '-0.04797', '0.1324', '0.3398', '0.1614', '0.355', '-0.2', '-0.1562', '0.03482', '-0.3425', '-0.2815', '0.1628', '0.24', '0.373', '0.1194', '-0.1033', '-0.93', '0.5073', '0.25', '-0.4463', '-0.569', '0.3643', '-0.3093', '0.1327', '6.92e-05', '-0.0195', '0.3567', '1.046', '0.1683', '-0.4138', '0.6294', '-0.219', '0.03403', '0.4724', '-0.106', '0.595', '0.002497', '-0.7876', '0.3298', '0.3347', '-0.242', '0.6724', '0.7314', '0.9473', '-0.1594', '0.5854', '-0.144', '-0.0923', '0.762', '0.421', '0.3118', '0.4583', '0.697', '0.112', '0.1371', '0.585', '-0.0321', '0.5894', '-0.621', '0.8555', '0.2988']",,,,,,,
mondo:0007084,familial focal alopecia,"['alopecia, familial focal', 'ALPF']",,104110,,C1863092,,,,C566301,,,,
mondo:0007085,alopecia-epilepsy-pyorrhea-intellectual disability syndrome,"['congenital universal alopecia, epilepsy, mental subnormality and pyorrhea', 'Shokeir syndrome', 'alopecia, psychomotor epilepsy, pyorrhea, and mental subnormality', 'alopecia, epilepsy, pyorrhea, mental subnormality']",,104130,1008,C1863090,,,,C537057,,,,
mondo:0007086,autosomal dominant Alport syndrome,"['renal failure and sensorineural hearing loss', 'Alport syndrome 3, autosomal dominant', 'Alport syndrome, autosomal dominant', 'Alport syndrome dominant type']",0110032,104200,88918,,"['0.08453', '0.4033', '-0.06235', '0.0785', '0.1354', '-0.4502', '-0.2373', '0.3335', '-0.2375', '-0.363', '0.05066', '-0.2295', '-0.4438', '0.2482', '0.1262', '-0.4731', '0.07104', '-0.2627', '0.1141', '0.04285', '-0.1875', '-0.2245', '-0.05365', '-0.10425', '0.4421', '-0.0759', '-0.2834', '-0.2487', '0.22', '0.12085', '0.2935', '-0.00874', '0.3845', '0.0753', '0.1015', '-0.2878', '0.003433', '-0.1449', '0.02429', '0.1625', '0.01958', '0.07904', '-0.1425', '-0.06726', '-0.2676', '-0.2041', '-0.3616', '-0.11633', '0.1385', '0.2145', '0.0936', '0.1764', '0.2362', '-0.3625', '0.2327', '-0.548', '0.3684', '0.11926', '-0.1481', '-0.0179', '0.1954', '-0.2172', '0.267', '-0.04178', '-0.2064', '-0.0784', '0.0923', '0.4436', '-0.3638', '0.449', '-0.1857', '-0.04578', '0.1196', '-0.3928', '0.4026', '-0.0719', '-0.1088', '0.4924', '-0.2349', '0.1615', '0.1797', '-0.10425', '0.1681', '0.5894', '-0.0919', '-0.3071', '0.3083', '0.03168', '0.083', '0.7617', '-0.1356', '0.2084', '-0.053', '0.1027', '0.7666', '-0.0779', '0.218', '-0.3804', '-0.10486', '0.3276']",,,,,,,
mondo:0007087,alternating hemiplegia of childhood 1,"['ATP1A2 alternating hemiplegia of childhood', 'alternating hemiplegia of childhood type 1', 'AHC1', 'alternating hemiplegia of childhood 1', 'alternating hemiplegia of childhood caused by mutation in ATP1A2']",,104290,,C3549447,,,,,,,,
mondo:0007088,Alzheimer disease type 1,"['Alzheimer disease, familial, 1', 'Alzheimer disease, early-onset, with cerebral amyloid angiopathy', 'presenile and senile dementia', 'Alzheimer disease', 'Alzheimer disease, susceptibility to', 'Alzheimer disease 1', 'Alzheimer disease, late-onset, susceptibility to', 'AD1', 'early-onset familial form of Alzheimer disease', 'AD', 'Alzheimer disease 1, familial', 'Alzheimer disease, protection against']",0080348,104300,,C2931257,,,,C536594,,,,
mondo:0007089,Alzheimer disease 2,"['Alzheimer^s disease type 2', 'AD2', 'Alzheimer disease type 2', 'Alzheimer disease associated with APOE E4', 'Alzheimer^s disease 2', 'Alzheimer disease 2', 'Alzheimer disease associated with APOE4', 'late onset Alzheimer disease', 'Alzheimer disease 2, late-onset', 'late-onset familial alzheimer disease', 'LOFAD', 'late onset familial Alzheimer disease', 'Alzheimer disease 2, late onset', 'Alzheimer disease-2']",0110035,104310,,C1863051,,,,C536595,,,,
mondo:0007090,"amastia, bilateral, with ureteral triplication and dysmorphism","['amastia, bilateral, with ureteral triplication and dysmorphism']",,104350,,C1863015,,,,C566295,,,,
mondo:0007091,amelia and terminal transverse hemimelia,['amelia and terminal transverse hemimelia'],,104400,,C1863014,,,,C566294,,,,
mondo:0007092,amelogenesis imperfecta type 1B,"['amelogenesis imperfecta, type 1B', 'AI1B', 'amelogenesis imperfecta type IB', 'ENAM amelogenesis imperfecta', 'hereditary localized enamel hypoplasia', 'amelogenesis imperfecta, hypoplastic local, autosomal dominant', 'amelogenesis imperfecta, type IB', 'amelogenesis imperfecta caused by mutation in enam', 'AIH2', 'enamel hypoplasia, hereditary localized', 'enamel hypoplasia, hereditary localised', 'hereditary localised enamel hypoplasia', 'enam amelogenesis imperfecta', 'autosomal dominant hypoplastic local amelogenesis imperfecta']",0110052,104500,,C0399368,,,,C562879,520.5,,,
mondo:0007093,hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism,"['amelogenesis imperfecta caused by mutation in DLX3', 'amelogenesis imperfecta type 4', 'AI4', 'amelogenesis imperfecta hypomaturation-hypoplastic type with taurodontism', 'amelogenesis imperfecta, hypomaturation-hypoplastic type, with taurodontism', 'amelogenesis imperfecta, type IV', 'AIHHT', 'DLX3 amelogenesis imperfecta', 'amelogenesis imperfecta, type 4']",0110053,104510,100034,C1863012,"['-0.1381', '0.1102', '0.1444', '-0.0416', '0.097', '-0.2058', '-0.03032', '0.2054', '-0.1958', '-0.1255', '-0.1077', '-0.0764', '-0.135', '-0.0804', '0.1371', '-0.1362', '0.0492', '-0.10077', '-0.0774', '-0.2896', '0.08136', '-0.02667', '0.1882', '-0.03888', '0.1288', '0.1334', '-0.07947', '0.004196', '0.0313', '-0.06635', '-0.03296', '0.06885', '0.1016', '0.1395', '0.2612', '-0.1284', '0.0294', '-0.1957', '-0.0421', '-0.2861', '0.03061', '-0.2025', '0.0893', '-0.1092', '-0.1925', '-0.1625', '0.07526', '0.1989', '0.1819', '0.01069', '0.1602', '-0.1401', '0.13', '-0.02524', '-0.1123', '-0.1699', '0.2964', '-0.0929', '-0.1515', '0.09155', '0.08185', '0.09406', '0.04214', '-0.1065', '0.08435', '0.10706', '0.12024', '0.0877', '-0.11755', '0.1376', '-0.2019', '-0.012085', '0.0653', '-0.2408', '0.1608', '0.0009713', '0.01868', '-0.012634', '-0.08105', '-0.06247', '-0.001402', '0.02965', '-0.08203', '0.1578', '-0.0941', '-0.10455', '0.02863', '0.237', '0.2866', '0.05173', '-0.0191', '0.02725', '0.01901', '0.04077', '0.3718', '0.07654', '0.2236', '-0.2798', '0.0874', '-0.0619']",,,C566293,,,,
mondo:0007094,amelogenesis imperfecta type 1A,"['amelogenesis imperfecta local hypoplastic', 'LAMB3 amelogenesis imperfecta', 'amelogenesis imperfecta caused by mutation in LAMB3', 'AI1A', 'amelogenesis imperfecta, hypoplastic type 1A', 'amelogenesis imperfecta, type IA', 'local hypoplastic amelogenesis imperfecta', 'amelogenesis imperfecta type IA', 'amelogenesis imperfecta hypoplastic type IA', 'amelogenesis imperfecta, type 1A']",0110054,104530,,,,,,C538240,,,,
mondo:0007095,ameloonychohypohidrotic syndrome,"['ameloonychohypohidrotic syndrome', 'hypocalcified-hypoplastic enamel, onycholysis with subungual hyperkeratosis, and hypohidrosis', 'amelo-onycho-hypohidrotic syndrome']",,104570,1028,C1863006,,,,C538245,,,,
mondo:0007096,amenorrhea-galactorrhea syndrome,['amenorrhea-galactorrhea syndrome'],,104600,,C0271556,,,,C537072,253.1,,,
mondo:0007097,Finnish type amyloidosis,"['gelsolin amyloidosis', 'amyloidosis, Finnish type', 'AGel amyloidosis', 'lattice corneal dystrophy type II Finnish', 'amyloidosis V', 'lattice corneal dystrophy, type 2', 'cerebral amyloid angiopathy, Gsn-related', 'corneal dystrophy, lattice type 2', 'amyloidosis due to mutant gelsolin', 'amyloidosis 5', 'amyloid cranial neuropathy with lattice corneal dystrophy', 'amyloidosis, Meretoja type', 'hereditary amyloidosis, Finnish type', 'familial amyloidosis, Finnish type', 'hereditary gelsolin amyloidosis', 'amyloidosis, MERETOJA type', 'familial amyloid polyneuropathy type IV']",0050637,105120,85448,,"['0.4558', '-0.804', '-0.518', '0.2323', '0.0513', '-0.3748', '-0.7266', '0.383', '-1.277', '-0.01207', '-0.4', '-0.0884', '-1.185', '0.3306', '-0.874', '-0.02989', '0.00265', '-0.3044', '-0.05338', '-0.789', '0.5356', '-0.1938', '0.5312', '0.1031', '-0.0855', '0.632', '-0.5557', '-0.3582', '0.569', '0.356', '0.316', '-0.3247', '0.844', '-0.6987', '0.554', '-0.7764', '-0.214', '0.2808', '0.2189', '-0.1716', '0.0574', '-0.05386', '0.0639', '0.4673', '0.2493', '-0.616', '-0.3618', '0.608', '0.2396', '0.728', '-0.0618', '0.8096', '0.3286', '-0.3809', '-0.578', '-0.2206', '0.5996', '0.1788', '-0.5537', '-0.817', '-0.276', '0.248', '0.581', '-0.714', '0.10754', '-0.511', '0.2693', '1.118', '-0.817', '0.3604', '-0.4595', '0.6396', '-0.582', '-0.2256', '0.281', '0.573', '-0.3545', '1.052', '-0.3809', '-0.816', '-0.1466', '-0.383', '-0.1785', '-0.00462', '0.1149', '-0.4192', '-0.089', '-0.1118', '0.04932', '-0.1516', '0.6846', '-0.2527', '-0.382', '-0.2045', '0.716', '0.4', '-0.661', '-0.1403', '0.1887', '0.01865']",,,C537459,277.39,,,
mondo:0007098,ACys amyloidosis,"['amyloidosis 6', 'hereditary cerebral hemorrhage with amyloidosis', 'cystatin amyloidosis', 'cerebral amyloid angiopathy, CST3-related', 'hereditary cerebral haemorrhage with amyloidosis', 'hereditary cystatin C amyloid angiopathy', 'cerebral hemorrhage, hereditary, with amyloidosis', 'cerebral amyloid angiopathy', 'CST3-related cerebral amyloid angiopathy', 'CST3-related amyloidosis', 'amyloidosis VI', 'amyloidosis, Cerebroarterial, Icelandic type', 'hereditary cerebral haemorrhage with amyloidosis, Icelandic type', 'hereditary cerebral hemorrhage with amyloidosis, Icelandic type', 'HCHWA, Icelandic type']",0070027,105150,100008,,"['0.371', '-0.5874', '-0.745', '0.194', '0.1462', '-0.312', '-0.727', '0.4524', '-1.481', '0.2214', '-0.2408', '0.01912', '-0.9067', '0.0703', '-0.5044', '-0.3289', '0.0951', '-0.1385', '-0.0344', '-0.5483', '0.5093', '0.1667', '0.4036', '0.1038', '0.0621', '0.655', '-0.6406', '0.04144', '0.451', '0.555', '0.4312', '-0.3855', '1.153', '-0.8115', '0.4365', '-0.699', '-0.4827', '0.3933', '0.255', '-0.0865', '0.3857', '-0.5947', '-0.1219', '0.4404', '0.4905', '-0.4714', '-0.396', '0.1071', '0.4602', '0.797', '0.2428', '0.8994', '0.1497', '-0.1676', '-0.5137', '-0.2173', '0.812', '0.1001', '-0.458', '-0.7715', '-0.6387', '0.2383', '0.723', '-0.7705', '0.522', '-0.10864', '0.3574', '0.727', '-0.787', '0.2266', '-0.4236', '0.01807', '-0.4595', '-0.1715', '0.516', '0.666', '-0.1813', '1.663', '-0.5684', '-0.5146', '-0.619', '-0.592', '0.1614', '-0.1531', '0.3496', '-0.5103', '0.0502', '0.07855', '0.3486', '-0.151', '0.564', '-0.1334', '-0.479', '-0.526', '0.487', '0.5347', '-0.6216', '-0.36', '0.09296', '0.1101']",,,,437.8,,,
mondo:0007099,familial visceral amyloidosis,"['amyloidosis familial renal', 'Ostertag type amyloidosis', 'amyloidosis, renal', 'amyloidosis 8', 'German type amyloidosis', 'amyloidosis, systemic Nonneuropathic', 'familial amyloid nephropathy', 'hereditary renal amyloidosis', 'amyloidosis, 3 or more types', 'amyloidosis VIII', 'familial renal amyloidosis', 'hereditary amyloid nephropathy', 'hereditary amyloidosis with primary renal involement', 'amyloidosis, Ostertag type', 'amyloidosis systemic nonneuropathic', 'amyloidosis familial visceral', 'amyloidosis, familial visceral', 'amyloidosis, familial renal', 'systemic nonneuropathic amyloidosis']",0050636,105200,85450,C0268389,"['0.5913', '-0.844', '-0.4885', '0.1004', '0.1456', '-0.356', '-0.7656', '0.2917', '-1.191', '-0.1018', '-0.2355', '-0.1257', '-1.144', '0.309', '-0.806', '-0.02266', '0.012024', '-0.3208', '0.0715', '-0.6934', '0.4429', '-0.06506', '0.6006', '-0.1508', '0.2335', '0.545', '-0.593', '-0.149', '0.4736', '0.2412', '0.3496', '-0.552', '0.965', '-0.623', '0.3975', '-0.858', '-0.3213', '0.2203', '0.2074', '-0.1697', '0.276', '-0.10516', '0.05646', '0.3289', '0.3616', '-0.7676', '-0.6606', '0.357', '0.342', '0.9863', '-0.1313', '0.643', '0.3113', '-0.4502', '-0.587', '-0.1262', '0.5186', '0.1824', '-0.6196', '-0.881', '-0.3833', '0.495', '0.5156', '-0.6646', '0.10486', '-0.4666', '0.4182', '0.936', '-0.766', '0.2244', '-0.4429', '0.5913', '-0.469', '-0.1969', '0.2316', '0.671', '-0.3923', '1.114', '-0.363', '-0.805', '-0.3892', '-0.2285', '0.02167', '-0.2224', '0.4324', '-0.5347', '-0.1771', '-0.1991', '0.1619', '-0.2458', '0.667', '-0.4365', '-0.527', '-0.297', '0.765', '0.659', '-0.663', '-0.4307', '-0.0981', '0.0439']",,,C538249,277.39,,,
mondo:0007100,familial amyloid neuropathy,"['familial amyloid polyneuropathy, Portuguese-Swedish-Japanese type', 'transthyretin amyloid polyneuropathy', 'ATTRV30M-related amyloidosis', 'hereditary amyloidosis, transthyretin-related', 'amyloid cardiomyopathy, transthyretin-related', 'ATTRV30M amyloidosis', 'Corino de Andrade^s disease', 'TTR amyloidosis', 'paramyloidosis', 'amyloid Neuropathies, familial', 'familial amyloid polyneuropathy type I (Portuguese-Swedish-Japanese type)', 'transthyretin amyloid neuropathy', 'amyloidosis transthyretin related', 'TTR amyloid neuropathy', 'amyloidosis, hereditary, transthyretin-related', 'amyloidosis, leptomeningeal, transthyretin-related', 'familial amyloid polyneuropathy', 'familial transthyretin amyloidosis', 'transthyretin amyloidosis', 'familial amyloid polyneuropathy type I', 'transthyretin-related hereditary amyloidosis', 'amyloid polyneuropathy, familial']",0050761,105210,85447,C2751492,"['-0.1271', '-0.11395', '-0.1881', '0.325', '0.4104', '-0.03293', '-0.02045', '0.6655', '-0.1672', '0.1729', '-0.59', '-0.72', '-0.139', '0.4148', '-0.2097', '0.409', '-0.2047', '-0.8145', '-0.1926', '-0.545', '0.8755', '-0.486', '0.444', '0.2842', '0.01724', '-0.00765', '0.1387', '-0.2866', '-0.2915', '0.01567', '0.9487', '0.2385', '0.1423', '-0.4219', '0.12177', '-0.6416', '-0.1868', '-0.2817', '-0.02863', '0.2573', '-0.1562', '-0.1522', '0.8364', '0.11206', '0.6733', '-0.3696', '-0.4373', '0.2507', '-0.01102', '0.4268', '-0.2264', '0.545', '-0.06064', '-0.403', '0.1583', '-0.3164', '0.7085', '0.1863', '-0.7397', '-0.2455', '0.1766', '-0.1649', '0.4333', '0.0094', '-0.341', '0.528', '0.2732', '0.557', '-0.10126', '0.2588', '-0.2822', '0.005604', '-0.2998', '-0.1267', '0.7437', '0.4314', '0.3584', '0.528', '-0.1527', '-0.897', '0.1115', '-0.8013', '-0.1667', '0.509', '-0.1705', '-0.3528', '0.4463', '-0.202', '0.10126', '-0.602', '0.553', '-0.5557', '-0.066', '-0.2837', '0.5146', '-0.2273', '0.1195', '-0.1886', '-0.00786', '0.0527']",C84554,0004129,C567782,277.39,,,
mondo:0007101,familial primary localized cutaneous amyloidosis,"['FPLCA', 'hereditary primary cutaneous amyloidosis', 'primary localized cutaneous amyloidosis', 'primary localised cutaneous amyloidosis']",,,353220,CN204529,"['0.3552', '-0.7295', '-0.5283', '0.1384', '0.1669', '-0.342', '-0.799', '0.1875', '-1.246', '0.1569', '-0.3284', '-0.002487', '-1.183', '0.2625', '-0.794', '0.04364', '0.188', '-0.09937', '0.125', '-0.7217', '0.4744', '-0.1887', '0.6445', '-0.0278', '0.1753', '0.7754', '-0.4224', '-0.1317', '0.2172', '0.2922', '0.376', '-0.544', '0.847', '-0.7983', '0.572', '-0.6357', '-0.2625', '0.3628', '0.314', '-0.2588', '-0.00789', '-0.2422', '-0.0155', '0.2678', '0.1947', '-0.5767', '-0.6343', '0.2842', '0.4067', '0.703', '0.03757', '0.6646', '0.279', '-0.2472', '-0.727', '-0.1378', '0.625', '0.2124', '-0.782', '-0.901', '-0.351', '0.4507', '0.5405', '-0.799', '0.1103', '-0.1881', '0.512', '1.03', '-0.4812', '0.61', '-0.352', '0.3394', '-0.538', '-0.2803', '0.2039', '0.551', '-0.4956', '1.265', '-0.5063', '-0.925', '-0.505', '-0.316', '0.05142', '-0.3254', '0.1676', '-0.587', '-0.2211', '-0.2415', '0.1935', '0.02257', '0.4917', '-0.4182', '-0.5366', '-0.0697', '0.459', '0.2805', '-0.391', '-0.4304', '0.04984', '-0.007763']",,,C562643,,,,
mondo:0007102,amyotrophic dystonic paraplegia,['amyotrophic dystonic paraplegia'],,105300,,C1862956,,,,C566292,,,,
mondo:0007103,amyotrophic lateral sclerosis type 1,"['amyotrophic lateral sclerosis type 1', 'amyotrophic lateral sclerosis, familial', 'amyotrophic lateral sclerosis, autosomal dominant', 'amyotrophic lateral sclerosis 1', 'FALS', 'amyotrophic lateral sclerosis, sporadic, included', 'ALS1', 'amyotrophic lateral sclerosis 1, familial', 'amyotrophic lateral sclerosis 1, autosomal dominant', 'amyotrophic lateral sclerosis 1, autosomal recessive', 'amyotrophic lateral sclerosis, susceptibility to', 'amyotrophic lateral sclerosis 1, autosomal dominant amyotrophic lateral sclerosis 1, autosomal recessive, included', 'amyotrophic lateral sclerosis, sporadic']",0060193,105400,,,,,,C531617,,,,
mondo:0007104,amyotrophic lateral sclerosis-parkinsonism-dementia complex,"['amyotrophic lateral sclerosis-parkinsonism/dementia complex, susceptibility to', 'amyotrophic lateral sclerosis-Parkinsonism/dementia Complex of Guam', 'amyotrophic lateral sclerosis-Parkinsonism/dementia Complex type 1', 'amyotrophic lateral sclerosis-PARKINSONISM/dementia complex 1', 'Guam disease', 'Lytigo-Bodig disease', 'Parkinsonism-dementia-ALS complex', 'PDALS', 'amyotrophic lateral sclerosis-parkinsonism-dementia of Guam syndrome', 'amyotrophic lateral sclerosis, Parkinsonism/dementia complex of Guam', 'ALS-pDC', 'Lytico-Bodig disease']",0111246,105500,90020,,,,,,,G12.2,,
mondo:0007105,frontotemporal dementia and/or amyotrophic lateral sclerosis 1,"['frontotemporal dementia with motor neuron disease caused by mutation in C9ORF72', 'FTDALS1', 'C9ORF72 frontotemporal dementia with motor neuron disease', 'FTDMND', 'frontotemporal dementia and/or amyotrophic lateral sclerosis', 'frontotemporal dementia and/or motor neuron disease', 'amyotrophic lateral sclerosis and/or frontotemporal dementia', 'C9orf72 frontotemporal dementia with motor neuron disease', 'frontotemporal dementia and/or amyotrophic lateral sclerosis type 1', 'frontotemporal dementia and/or amyotrophic lateral sclerosis 1', 'ALSFTD']",0060213,105550,,C3888102,,C168756,,,,,,
mondo:0007106,anal sphincter dysplasia,"['ASDP', 'anal sphincter dysplasia']",,105563,,C1862936,,,,C538254,,,,
mondo:0007107,"anal sphincter myopathy, internal","['proctalgia fugax due to anal sphincter myopathy', 'anal sphincter myopathy, internal']",,105565,,C1862935,,,,C566287,,,,
mondo:0007108,anal canal carcinoma,"['anal canal and perianal gland cancer', 'carcinoma of anal canal', 'carcinoma of the anal canal', 'anal canal carcinoma', 'cloacogenic carcinoma', 'anal canal cancer', 'anal canal and perianal gland carcinoma']",6126,105580,424013,,,C7489,,C563020,,,,
mondo:0007109,congenital dyserythropoietic anemia type 3,"['CDAN3', 'CDA type III', 'congenital dyserythropoietic anemia type 3', 'CDA type 3', 'CDA 3', 'Erythroreticulosis, hereditary benign', 'anemia with multinucleated erythroblasts', 'anemia, congenital dyserythropoietic, type III', 'dyserythropoietic anemia, congenital, type III', 'dyserythropoietic Anemia, congenital, type 3', 'dyserythropoietic anemia, congenital type 3', 'anaemia with multinucleated erythroblasts', 'CDA III']",0111399,105600,98870,C0271934,,,,,285.8,,,
mondo:0007110,Diamond-Blackfan anemia 1,"['Diamond-Blackfan anaemia caused by mutation in RPS19', 'DBA1', 'Diamond-Blackfan anemia caused by mutation in RPS19', 'Diamond-Blackfan Anemia type 1', 'anemia, congenital hypoplastic, of Blackfan and Diamond', 'Aase syndrome', 'Red cell aplasia, Pure, hereditary', 'RPS19 Diamond-Blackfan anemia', 'Diamond-Blackfan anemia 1', 'DBA', 'Blackfan-Diamond syndrome', 'anemia, congenital erythroid hypoplastic', 'Aase-Smith syndrome 2', 'Diamond-Blackfan Anaemia type 1', 'RPS19 Diamond-Blackfan anaemia', 'aregenerative Anemia, chronic congenital', 'erythrogenesis imperfecta']",0111895,105650,,C2676137,,C176911,,C567302,,,,
mondo:0007111,"aneurysm, intracranial berry type 1","['aneurysmal subarachnoid hemorrhage, familial', 'ANIB1', 'aneurysm, intracranial berry, 1']",0080964,105800,,C1862932,,,,C566284,,,,
mondo:0007112,interventricular septum aneurysm,['aneurysm of interventricular septum'],,105805,99092,C1387721,,,,C563239,,,,
mondo:0007113,Angelman syndrome,"['AS', 'happy puppet syndrome (formerly)', 'Angelman syndrome (Type 2)', 'Angelman syndrome', 'Angelman syndrome (Type 1)', 'puppetlike syndrome', 'happy puppet syndrome, formerly', 'Angelman syndrome chromosome region', 'happy puppet syndrome']",1932,105830,72,C0162635,"['0.2391', '0.7925', '0.1244', '-0.12366', '-0.144', '-0.7285', '-0.285', '0.3442', '-0.3833', '-0.662', '0.3796', '0.1079', '0.06726', '0.3035', '-0.05164', '0.2837', '-0.04355', '-0.1207', '-0.66', '-0.4492', '-0.589', '0.1158', '-0.1467', '0.03592', '0.1582', '-0.5874', '0.2034', '-0.4158', '0.2102', '-0.09094', '0.5737', '-0.527', '0.4023', '-0.1697', '-0.4346', '-0.1267', '-0.1272', '-0.1348', '-0.09546', '-0.7393', '0.3572', '0.1898', '-0.3535', '0.03766', '-0.11536', '-0.906', '-0.5034', '-0.5356', '0.17', '0.5127', '-0.1614', '-0.1946', '-0.5703', '-0.565', '0.02429', '-0.3186', '-0.368', '0.7017', '0.236', '0.04163', '0.0457', '0.41', '0.188', '0.2235', '-0.1464', '-0.1307', '0.12054', '0.1016', '-0.562', '0.4727', '-0.0453', '0.7925', '-0.0497', '-0.4934', '0.1171', '0.411', '0.0785', '-0.5625', '-0.3794', '0.1053', '0.6704', '-0.2013', '0.1426', '0.00924', '0.431', '0.1766', '0.0633', '0.312', '0.4824', '0.491', '-0.156', '0.311', '-0.5093', '-0.08344', '0.2988', '-0.251', '-0.1593', '-0.6343', '0.348', '-0.1169']",C75462,,D017204,759.89,Q93.51,10049004,
mondo:0007114,Angel-shaped phalango-epiphyseal dysplasia,"['ASPED', 'Angel shaped phalangoepiphyseal dysplasia', 'Angel-shaped phalangoepiphyseal dysplasia']",,105835,63442,,,,,C536361,,,10066017,
mondo:0007115,"angioma serpiginosum, autosomal dominant","['angioma serpiginosum, autosomal dominant', 'autosomal dominant angioma serpiginosum']",,106050,,C1970130,,,,C536365,,,,
mondo:0007116,hereditary neurocutaneous angioma,"['hemangiomatosis, disseminated', 'angioma hereditary neurocutaneous', 'angioma, hereditary neurocutaneous', 'hereditary neurocutaneous malformation', 'hereditary neurocutaneous angioma', 'spinal arterial Venous malformations with cutaneous hemangiomas']",,106070,1062,,,,,,,,,
mondo:0007118,isolated anhidrosis with normal sweat glands,"['Dann-Epstein-Sohar syndrome', 'isolated generalised anhidrosis with normal sweat glands', 'ITPR2 anhidrosis', 'isolated generalized anhidrosis with normal sweat glands', 'anhidrosis, isolated, with normal sweat glands', 'ANHD', 'anhidrosis caused by mutation in ITPR2']",0060603,106190,468666,C1862871,,,,,,,,
mondo:0007119,isolated aniridia,"['aniridia without systemic involvement', 'nonsyndromic aniridia']",,,250923,,"['-0.231', '-0.1582', '-0.1458', '0.3032', '0.1593', '0.2861', '0.5137', '0.7515', '-0.2177', '-0.6377', '-0.2205', '-0.3442', '-0.05682', '0.2465', '-0.2524', '-0.472', '0.429', '-0.4485', '0.0787', '-0.941', '-0.2969', '0.1288', '0.607', '-0.0761', '-0.2148', '-0.03534', '-0.2598', '0.327', '-0.1786', '0.4253', '0.9277', '0.1936', '0.1676', '0.373', '-0.4858', '0.2703', '0.595', '-0.4604', '-0.05', '-0.361', '0.552', '0.12067', '0.4182', '-0.418', '-0.015045', '0.1436', '0.1355', '-0.2625', '0.2361', '-0.301', '0.3103', '0.0662', '0.0922', '-0.5444', '0.0638', '0.03177', '0.5903', '-0.1519', '-0.87', '-0.3127', '-0.05414', '-0.0478', '0.4995', '0.2267', '-0.2327', '0.1466', '0.3794', '0.1277', '-0.1481', '0.1831', '-0.3098', '0.2883', '-0.0292', '-0.2407', '0.2468', '-0.2754', '0.4404', '-0.1842', '-0.2031', '0.0689', '-0.2815', '0.4778', '-0.02994', '0.907', '-0.2174', '-0.5894', '0.3152', '0.2766', '0.1858', '0.1921', '0.04355', '0.605', '0.014656', '-0.1654', '0.595', '-0.4817', '0.5527', '-0.0775', '0.1829', '0.2297']",,,,,,,
mondo:0007120,aniridia-absent patella syndrome,"['aniridia absent patella', 'familial syndrome of aniridia and absence of the patella', 'aniridia and absent patella']",,106220,1069,C1862868,,,,C566281,,,,
mondo:0007121,"aniridia, microcornea, and spontaneously Reabsorbed cataract","['aniridia, microcornea, and spontaneously Reabsorbed cataract']",,106230,,C1862867,,,,C566280,,,,
mondo:0007122,anisocoria,"['anisocoria (disease)', 'anisocoria']",,106240,,,,,,D015875,379.41,,,0009916
mondo:0007123,ankyloblepharon filiforme adnatum-cleft palate syndrome,"['congenital filiform fusion of the eyelids with cleft palate and/or cleft lip', 'AFA', 'ankyloblepharon filiforme adnatum and cleft palate', 'ankyloblepharon filiforme adnatum cleft palate', 'ankyloblepharon filiforme adnatum', 'ankyloblepharon filiforme congenitum']",,106250,1072,C1302999,,,,C536373,,,,
mondo:0007124,ankyloblepharon-ectodermal defects-cleft lip/palate syndrome,"['Rapp-Hodgkins syndrome', 'Ankyloblepharon-ectodermal defects-cleft lip and palate syndrome', 'Hay-Wells syndrome', 'cleft palate, ankyloblepharon, alveolar synechiae, and ectodermal defects', 'ankyloblepharon-ectodermal defects-cleft LIP/palate', 'Ankyloblepharon ectodermal defects cleft lip/palate', 'Seres-Santamaria Arimany Muniz syndrome', 'AEC syndrome']",0090119,106260,1071,,"['0.885', '-0.08734', '0.3745', '-0.688', '0.695', '0.001112', '0.0823', '0.6265', '-0.35', '-0.598', '0.1373', '0.1981', '-0.4026', '0.2405', '-0.4658', '0.4355', '0.0857', '-0.3206', '-0.2428', '-0.8154', '-0.2554', '-0.03052', '0.2769', '-0.1373', '0.3784', '0.2406', '-0.803', '0.3494', '0.803', '-0.7686', '0.2096', '-0.3982', '0.2089', '0.1323', '0.1923', '0.161', '-0.337', '-0.632', '-0.1525', '-0.2227', '0.0481', '0.164', '0.3523', '0.2123', '-0.245', '-0.3193', '-0.299', '0.0912', '0.513', '-0.1067', '-0.459', '-0.12415', '-0.04318', '-0.0814', '-0.664', '-0.1387', '0.5405', '-0.0642', '-0.1638', '0.1249', '0.4326', '0.8154', '-0.516', '0.1776', '0.5225', '-0.505', '0.006695', '0.384', '0.3054', '0.9023', '-0.3772', '-0.2358', '-0.268', '-0.2024', '-0.005344', '-0.4163', '-0.001502', '-0.4827', '-0.3662', '-0.2474', '0.267', '-0.2225', '-0.08984', '0.1825', '-0.01962', '0.3232', '-0.502', '0.493', '0.1214', '0.608', '0.149', '0.4316', '-0.505', '0.85', '0.569', '-0.3796', '0.3074', '-0.4534', '0.4011', '0.558']",,,C535847,,,,
mondo:0007125,ankyloglossia,"['FUSED to floor of mouth', 'tongue-tie', 'ankyloglossia', '^tongue-Tie^']",0060604,106280,,,,C124538,,D000072676,750.0,Q38.1,,
mondo:0007126,"spondyloarthropathy, susceptibility to, 1","['spondyloarthropathy, susceptibility to, type 1', 'Bechterew syndrome', 'HLA-B spondyloarthropathy, susceptibility to', 'susceptibility to spondyloarthropathy 1', 'SPDA1', 'ankylosing spondylitis, susceptibility to', 'spondyloarthropathy, susceptibility to, 1', 'spondyloarthropathy, susceptibility to caused by mutation in HLA-B', 'Marie-Strumpell spondylitis']",0080603,106300,,,,,,,,,,
mondo:0007127,diffuse idiopathic skeletal hyperostosis,"['Forestier^s disease', 'dish', 'ankylosing vertebral hyperostosis', 'diffuse idiopathic skeletal hyperostosis', 'ankylosing vertebral hyperostosis with tylosis', 'disseminated idiopathic skeletal hyperostosis', 'Forestier disease']",6652,,2206,C0020498,,C84671,0007236,D004057,733.99,,,
mondo:0007128,annular erythema,['annular erythema'],,106500,,C0234906,,,,C562461,,,,
mondo:0007129,"tooth agenesis, selective, 1","['tooth agenesis, selective, 1', 'hypodontia/oligodontia 1', 'tooth agenesis, selective, with orofacial cleft', 'tooth agenesis caused by mutation in MSX1', 'tooth agenesis, selective, type 1', 'hypodontia/oligodontia with orofacial cleft', 'MSX1 tooth agenesis', 'tooth agenesis, selective, 1, with or without orofacial cleft', 'tooth agenesis, familial', 'STHAG1', 'second premolars and third molars, absence of']",,106600,,,,,,,,,,
mondo:0007130,congenital total pulmonary venous return anomaly,"['scimitar syndrome', 'total anomalous pulmonary venous return', 'scimitar anomaly', 'pulmonary venolobar syndrome', 'anomalous pulmonary Venous return', 'TAPVR1', 'total anomalous pulmonary VENOUS return 1', 'TAPVR']",4297,106700,99125,C0036400,,C98585,1001167,D012587,747.41,,,
mondo:0007131,anonychia with flexural pigmentation,['anonychia with flexural pigmentation'],,106750,69125,C1862844,,,,C566278,,,,
mondo:0007132,anonychia-ectrodactyly,"['anonychia-ectrodactyly', 'anonychia ectrodactyly']",,106900,,C1862843,,,,C566277,,,,
mondo:0007133,anonychia-onychodystrophy with brachydactyly type b and ectrodactyly,"['anonychia-onychodystrophy with brachydactyly type b and ectrodactyly', 'Kumar-Levick syndrome', 'autosomal dominant onychodystrophy and anonychia with type B brachydactyly and ectrodactyly']",,106990,2355,C1862842,,,,C536379,,,,
mondo:0007134,Cooks syndrome,"['anonychia-onychodystrophy with hypoplasia or absence of distal phalanges syndrome', 'ODP', 'Cooks syndrome', 'anonychia-onychodystrophy with hypoplasia or absence of distal phalanges', 'anonychia and absence/hypoplasia of distal phalanges']",,106995,1487,C1862841,,,,C537766,,,,
mondo:0007135,nonsyndromic congenital nail disorder 6,"['anonychia, partial', 'onychodystrophy-anonychia', 'nonsyndromic congenital nail disorder type 6', 'NDNC6', 'anonychia/hyponychia and onychodystrophy', 'nail disorder, nonsyndromic congenital, 6', 'absent nails and dystrophic nails']",0080084,107000,90390,C1862840,,,,,,,,
mondo:0007136,hereditary anorectal anomalies,"['genetic anorectal anomalies', 'anorectal anomalies']",,107100,,,,,,C567938,,,,
mondo:0007137,isolated congenital anosmia,"['ANIC', 'anosmia, congenital', 'anosmia, isolated congenital', 'congenital anosmia']",,107200,88620,,,,,C535983,,,,
mondo:0007138,anterior segment dysgenesis 1,"['anterior segment mesenchymal dysgenesis', 'ASGD1', 'anterior segment dysgenesis 1', 'anterior segment dysgenesis 1, multiple subtypes', 'anterior segment ocular dysgenesis', 'ASMD']",0080606,107250,,C1862839,,,,,,,,
mondo:0007142,Townes-Brocks syndrome,"['deafness, sensorineural, with imperforate anus and hypoplastic thumbs', 'renal-ear-anal-radial syndrome', 'Townes-Brocks syndrome 1', 'rear syndrome', 'deafness, sensorineural, with imperforate anus and thumb anomalies', 'renal-Ear-anal-radial syndrome', 'imperforate anus with hand, foot and ear anomalies', 'anus, imperforate, with hand, foot, and Ear anomalies', 'sensorineural deafness with imperforate anus and hypoplastic thumbs', 'Townes-Brocks syndrome', 'Townes-Brocks-branchiootorenal-like syndrome', 'TBS', 'anus, imperforate, with hand, foot and ear anomalies', 'Townes syndrome', 'TBS1']",0050887,,857,CN034849,"['-0.0849', '-0.111', '0.3652', '-0.375', '0.4768', '0.1274', '0.3374', '1.076', '-0.237', '-0.6562', '-0.2688', '-1.164', '-0.3147', '-0.06018', '-0.528', '-0.3303', '-0.1581', '-0.594', '0.2183', '-0.494', '0.0631', '0.112', '0.2181', '-0.0706', '0.1375', '0.03918', '-0.4407', '0.2233', '1.084', '-0.044', '0.2776', '0.083', '-0.10657', '0.283', '0.1981', '-0.8677', '-0.3909', '-0.7646', '-0.2737', '0.1978', '0.0937', '0.63', '0.5044', '-0.2673', '0.4468', '-0.413', '0.406', '0.475', '-0.2856', '0.1914', '-0.526', '0.3203', '-0.0787', '-0.996', '-0.362', '-0.1653', '0.3145', '-0.06204', '-0.5376', '0.2004', '-0.0063', '0.0934', '-0.0596', '0.08636', '-0.06964', '0.01845', '0.04297', '0.7954', '-0.3882', '0.3174', '-0.1099', '0.03915', '0.1989', '0.2343', '0.717', '0.11115', '-0.02773', '-0.229', '-0.3042', '-0.08417', '0.01843', '-0.1812', '0.004887', '0.06854', '0.2773', '-0.2031', '0.5996', '0.3186', '-0.3943', '-0.2219', '-0.3237', '0.08325', '0.2152', '0.2627', '0.846', '-0.02008', '0.3933', '-0.5044', '0.298', '0.793']",C99085,,C536974,759.89,,,
mondo:0007143,aortic arch anomaly-facial dysmorphism-intellectual disability syndrome,"['aortic arch anomaly - peculiar facies - intellectual disability', 'aortic arch anomaly-peculiar facies-intellectual disability syndrome', 'aortic arch anomaly with peculiar facies and intellectual disability', 'aortic arch anomaly with peculiar facies and mental retardation', 'familial syndrome of right-sided aortic arch, mental deficiency, and facial dysmorphism']",,107500,1110,C1862682,,,,C537785,,,,
mondo:0007144,"aortic arch interruption, facial palsy, and retinal coloboma","['aortic arch interruption, facial palsy, and retinal coloboma']",,107550,,C1862681,,,,C566271,,,,
mondo:0007145,aplasia cutis congenita,"['aplasia cutis congenita, nonsyndromic', 'aplasia cutis congenita nonsyndromic', 'scalp defect congenital', 'aplasia cutis congenita', 'congenital defect of skull and scalp', 'aplasia cutis congenita recessive', 'aplasia cutis congenita (disease)', 'ACC', 'scalp defect, congenital']",0080661,107600,1114,,"['-0.4304', '-0.1842', '-0.3674', '-0.2446', '0.7188', '0.03986', '0.2256', '-0.001357', '-0.4666', '-0.2776', '0.0905', '0.1189', '-0.0826', '-0.02748', '-0.517', '-0.00499', '0.2996', '-0.9775', '0.3242', '-0.97', '-0.3057', '-0.05975', '0.6855', '-0.389', '-0.522', '-0.31', '-0.7773', '0.3296', '0.09326', '0.2773', '0.603', '-0.4888', '-0.1365', '0.2417', '0.0994', '0.32', '-0.431', '-0.1764', '0.2642', '0.04352', '0.0868', '-0.05093', '0.09607', '-0.2727', '0.5356', '0.02151', '-0.057', '0.10376', '0.2922', '-0.3782', '0.4297', '-0.768', '0.3557', '-0.1617', '-0.825', '0.1736', '0.08905', '-0.006496', '-0.5703', '-0.0796', '0.0224', '0.2683', '-0.1893', '-0.058', '-0.2075', '0.2166', '0.9683', '0.1838', '-0.4163', '0.7446', '-0.5054', '0.05554', '-0.1279', '-0.3362', '0.1791', '-0.1401', '0.0727', '-0.0894', '0.1904', '-1.243', '-0.416', '-0.1436', '0.3923', '-0.1696', '-0.2262', '0.0751', '-0.078', '0.813', '-0.2896', '0.532', '0.227', '-0.01897', '-0.2866', '0.10406', '0.4739', '-0.6235', '0.2028', '-0.4998', '0.4858', '0.1561']",C98822,,,757.39,,,0001057
mondo:0007147,obstructive sleep apnea syndrome,"['Apneas, obstructive sleep', 'obstructive sleep apnea syndrome', 'obstructive sleep apnea', 'sleep Apneas, obstructive', 'sleep apnea syndrome, obstructive', 'syndrome, obstructive sleep apnea', 'syndrome, sleep apnea, obstructive', 'upper airway resistance sleep apnea syndrome', 'apnea, obstructive sleep', 'OSAHS', 'sleep apnea/hypopnea syndrome', 'syndrome, upper airway resistance, sleep apnea', 'Osa', 'sleep apnea hypopnea syndrome', 'obstructive sleep Apneas']",0050848,107650,,C0520679,,C27168,0003918,D020181,780.57,G47.33,,0002870
mondo:0007148,"appendicitis, proneness to","['appendicitis, susceptibility', 'appendicitis, proneness to']",,107700,,,,,,,,,,
mondo:0007150,arcus senilis,"['arcus corneae', 'arcus senilis', 'corneal arcus', 'arcus of cornea']",11342,107800,,C0003742,,,1000818,D001112,,,10003082,
mondo:0007151,"arms, malformation of","['arms, malformation of']",,107900,,,,,,C566258,,,,
mondo:0007152,arrhythmogenic right ventricular dysplasia 1,"['ARVC1', 'Uhl anomaly', 'familial arrhythmogenic right ventricular dysplasia 1', 'TGFB3 arrhythmogenic right ventricular cardiomyopathy', 'arrhythmogenic right ventricular dysplasia type 1', 'cardiomyopathy, right ventricular dilated', 'ARVD1', 'arrhythmogenic right ventricular cardiomyopathy 1', 'arrhythmogenic right ventricular dysplasia, familial, type 1', 'arrhythmogenic right ventricular cardiomyopathy caused by mutation in TGFB3', 'arrhythmogenic right ventricular dysplasia, familial, 1']",0110070,107970,3403,C1862511,,,,,,,,
mondo:0007153,"arteries, anomalies of","['arteries, anomalies of']",,108000,,,,,,,,,,
mondo:0007154,arteriovenous malformations of the brain,"['intracranial AVM', 'intracranial haemorrhage in brain arteriovenous malformations, susceptibility to', 'intracranial haemorrhage in brain cerebrovascular malformations, susceptibility to, somatic mutation', 'arteriovenous malformations of the brain', 'cerebral arteriovenous malformations', 'Bavm', 'cerebral arteriovenous malformation', 'intracranial hemorrhage in brain arteriovenous malformations, susceptibility to', 'intracranial arteriovenous malformation', 'intracranial hemorrhage in brain cerebrovascular malformations, susceptibility to, somatic mutation', 'arteriovenous malformation of the brain, somatic']",0060688,108010,46724,C0007772,,C2936,,D002538,,,,
mondo:0007155,"arteritis, familial granulomatous, with juvenile polyarthritis","['arteritis, familial granulomatous, with juvenile polyarthritis']",,108050,,C1862510,,,,C566253,,,,
mondo:0007156,"arthritis, sacroiliac","['arthritis, sacroiliac']",,108100,,C0748473,,,,C563037,,,,
mondo:0007157,"arthrogryposis, distal, type 1A","['arthrogryposis multiplex congenita, distal, type 1', 'arthrogryposis, distal, type 1', 'arthrogryposis multiplex congenita', 'DA1A', 'AMC', 'arthrogryposis, distal, type 1A', 'arthrogryposis, distal, type 2B4']",0111597,108120,,,,,,,,,,
mondo:0007158,arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome,"['arthrogryposis with oculomotor limitation and electroretinal abnormalities', 'oculomelic amyoplasia', 'distal arthrogryposis type IIB', 'Arthogryposis with oculomotor limitation and electroretinal abnormalities', 'distal arthrogryposis type 5', 'arthrogryposis ophthalmoplegia retinopathy', 'arthrogryposis, distal, type 2B', 'distal arthrogryposis with ophthalmoplegia', 'arthrogryposis, distal, type 5', 'arthrogryposis-oculomotor limitation-electroretinal anomalies syndrome', 'DA5', 'arthrogryposis- oculomotor limitation-electroretinal anomalies syndrome']",0111608,108145,1154,C1862472,"['-0.1759', '-0.1747', '0.202', '-0.606', '0.10095', '-0.2158', '-0.00393', '0.4045', '-0.7666', '-0.1428', '0.1353', '-0.04605', '-0.01955', '0.1472', '-0.1317', '-0.0744', '0.1117', '-0.0203', '-0.1958', '-0.8643', '-0.003256', '-0.1339', '0.2683', '0.1642', '-0.01605', '0.01188', '-0.2834', '0.10626', '0.001646', '0.1815', '0.1155', '0.2617', '0.3496', '0.1323', '-0.08966', '-0.343', '-0.01178', '-0.106', '0.0766', '0.0341', '0.3086', '-0.3726', '-0.07434', '0.1313', '-0.04367', '-0.1501', '-0.06525', '0.2279', '0.0807', '0.02959', '-0.4138', '0.1483', '0.1853', '-0.38', '-0.1262', '-0.51', '0.1171', '-0.4297', '-0.0454', '-0.284', '0.4785', '0.06064', '0.315', '0.2146', '-0.4395', '-0.1995', '0.1923', '0.3914', '-0.3809', '0.03784', '-0.3894', '0.1764', '0.0312', '-0.0853', '0.321', '-0.1306', '0.01319', '0.05798', '-0.4753', '-0.2852', '0.07874', '0.171', '0.4832', '0.3271', '-0.5205', '-0.000892', '-0.0518', '0.2042', '-0.0042', '0.02551', '0.1033', '0.4475', '0.1881', '0.1355', '0.516', '0.2964', '0.5645', '-0.416', '0.3035', '0.3748']",,,,,,,
mondo:0007159,arthrogryposis-like hand anomaly-sensorineural deafness syndrome,"['arthrogryposis, distal, type 6', 'arthrogryposis and sensorineural deafness', 'familial hand abnormality and sensori-neural deafness', 'DA6', 'distal arthrogryposis type 6', 'arthrogryposis-like hand anomaly and sensorineural deafness']",0111609,108200,1144,C1862471,,,,C535386,,,,
mondo:0007160,Stickler syndrome type 1,"['Stickler syndrome, type 1', 'Stickler syndrome, vitreous type 1', 'STL1', 'Stickler syndrome, membranous vitreous type', 'arthroophthalmopathy, hereditary progressive', 'Stickler syndrome, type I']",0080676,108300,90653,,"['0.7036', '0.3027', '-0.378', '0.428', '0.2935', '-0.7593', '-0.014046', '0.9346', '-1.051', '-0.5146', '0.3464', '-0.6343', '-0.12463', '1.06', '0.001229', '-0.0658', '-0.399', '0.5547', '-0.4805', '-0.005604', '-0.212', '0.1754', '0.3235', '0.1617', '-0.0313', '0.4634', '-0.9014', '0.1401', '1.055', '0.8457', '0.1787', '-0.1393', '-0.4146', '0.3286', '-0.199', '-0.11523', '-0.01991', '-0.12134', '-0.0782', '-0.4033', '0.5244', '0.3877', '-0.791', '-0.04324', '-0.4602', '-0.3667', '-0.01698', '0.04367', '0.3389', '-0.3684', '-0.4534', '0.5757', '0.586', '-0.1489', '0.4802', '-0.5366', '-0.3647', '0.1423', '0.1035', '-0.2189', '0.697', '0.06824', '-0.01087', '0.3208', '-0.2273', '0.4087', '0.2915', '0.4658', '-0.4092', '0.463', '0.08746', '0.574', '0.03806', '-0.518', '0.06177', '0.1434', '0.2944', '0.3875', '0.554', '0.738', '-0.06537', '-0.1606', '-0.2754', '0.764', '-0.8853', '-0.02574', '0.412', '0.5415', '0.3345', '0.312', '-0.637', '0.4658', '0.0652', '0.4175', '0.4421', '0.2693', '0.52', '-0.541', '-0.4072', '0.3572']",C168733,,C537492,,,,
mondo:0007161,spermatogenic failure 2,"['Aspermiogenesis Factor', 'spermatogenic failure 2', 'SPGF2']",0070164,108420,,,,,,,,,,
mondo:0007162,asymmetric short stature syndrome,['asymmetric short stature syndrome'],,108450,,C1862458,,,,C566248,,,,
mondo:0007163,episodic ataxia type 2,"['cerebellar ataxia, paroxysmal, Acetazolamide-responsive', 'ataxia, familial paroxysmal', 'CACNA1A hereditary episodic ataxia', 'ataxia, episodic, with Nystagmus', 'EA2', 'CAPA', 'episodic ataxia with nystagmus', 'ataxia, familial, paroxysmal', 'episodic ataxia, type 2', 'episodic ataxia type 2', 'hereditary episodic ataxia caused by mutation in CACNA1A', 'Cerebellopathy, hereditary paroxysmal', 'familial paroxysmal ataxia', 'Nystagmus-associated episodic ataxia', 'APCA', 'Acetazolamide-responsive episodic ataxia syndrome', 'Acetazolamide-responsive hereditary paroxysmal cerebellar ataxia', 'episodic ataxia, Nystagmus-associated', 'Acetazolamide-responsive, hereditary, paroxysmal, cerebellar ataxia']",0050990,108500,97,C1720416,"['-0.1984', '-0.3281', '0.04932', '-0.09015', '-0.176', '-1.099', '0.1093', '-0.07825', '-0.6025', '-0.7876', '0.1798', '0.4316', '-0.342', '0.2551', '0.4932', '-0.3591', '-0.1287', '-0.1692', '0.0742', '-0.8745', '0.1302', '-0.3176', '0.325', '-0.617', '0.5757', '-0.558', '-0.2822', '0.2412', '-0.01006', '-0.8755', '-0.02475', '0.514', '-0.469', '-0.1748', '0.1442', '0.0973', '-0.2517', '0.04303', '0.5186', '0.32', '0.333', '0.1649', '-0.3936', '0.4507', '0.558', '-0.5034', '0.1037', '0.477', '0.4546', '0.02257', '-0.11975', '0.2145', '-0.10785', '-0.3179', '-0.1495', '-0.7656', '0.4167', '0.7554', '-0.0858', '0.544', '-0.707', '0.4382', '0.345', '-0.04584', '-0.5513', '0.5435', '0.3984', '0.4702', '-0.674', '0.3965', '0.792', '0.4072', '-0.0681', '-0.84', '0.87', '0.34', '0.2686', '0.395', '0.1097', '0.5264', '-0.3347', '-0.9917', '0.2324', '0.7373', '-0.1871', '-0.682', '0.2074', '-0.1292', '0.4993', '0.654', '0.2517', '0.525', '0.1556', '0.1533', '1.06', '1.088', '0.33', '0.4536', '-0.637', '0.06183']",,,C535506,,,,
mondo:0007164,spastic ataxia 1,"['spastic ataxia 1, autosomal dominant', 'autosomal dominant spastic ataxia type 1', 'autosomal dominant spastic ataxia caused by mutation in VAMP1', 'spastic ataxia type 1', 'VAMP1 autosomal dominant spastic ataxia', 'SPAX1']",0050772,108600,251282,C1970107,"['-0.1749', '-0.3362', '0.04474', '-0.03638', '-0.3936', '-1.092', '0.0609', '-0.2383', '-0.6597', '-0.953', '0.084', '0.10516', '-0.2401', '0.2957', '0.567', '-0.2329', '-0.1055', '-0.226', '0.1176', '-0.853', '-0.0314', '-0.4006', '0.1664', '-0.674', '0.588', '-0.6685', '-0.3118', '0.265', '-0.1045', '-0.9077', '0.1696', '0.4934', '-0.5903', '-0.10297', '0.3796', '0.1567', '-0.2399', '0.07025', '0.4807', '0.324', '0.3357', '0.1473', '-0.3242', '0.3562', '0.3672', '-0.5586', '-0.004513', '0.442', '0.4185', '0.03152', '-0.08575', '0.1719', '-0.03787', '-0.3406', '-0.1716', '-0.886', '0.3696', '0.6543', '-0.0889', '0.5815', '-0.4504', '0.205', '0.324', '-0.1132', '-0.5713', '0.5903', '0.2524', '0.4573', '-0.553', '0.4497', '0.727', '0.4465', '-0.04938', '-0.927', '0.915', '0.3223', '0.0804', '0.2542', '0.01607', '0.4697', '-0.3777', '-0.7397', '0.4983', '0.96', '-0.09766', '-0.761', '0.3533', '-0.1799', '0.687', '0.5244', '0.5146', '0.377', '0.1554', '0.09216', '1.157', '0.9946', '0.4014', '0.402', '-0.5835', '-0.1066']",,,C566993,,G11.4,,
mondo:0007165,spastic ataxia 7,"['autosomal dominant spastic ataxia type 7', 'spastic ataxia type 7', 'spastic ataxia with congenital miosis', 'SPAX7', 'spastic ataxia 7, autosomal dominant', 'miosis, congenital, with spastic ataxia']",0050945,108650,1182,C1862441,,,,C566247,,G11.4,,
mondo:0007166,ataxia with fasciculations,['ataxia with fasciculations'],,108700,,C1862440,,,,C566246,,,,
mondo:0007167,atelosteogenesis type I,"['AOI', 'AO1', 'spondylo-humero-femoral dysplasia', 'spondylohumerofemoral hypoplasia', 'giant cell chondrodysplasia', 'atelosteogenesis, type I', 'atelosteogenesis type 1', 'atelosteogenesis, type 1']",,108720,1190,,"['-0.341', '0.8086', '-0.4426', '0.4849', '0.2642', '-0.5103', '-0.5503', '0.871', '-0.822', '-0.3074', '-0.157', '-0.167', '0.2803', '-0.367', '-0.3313', '0.3643', '0.607', '-0.4553', '-0.3674', '-0.679', '-0.1812', '0.00894', '1.291', '-0.08826', '0.214', '0.07635', '-0.2317', '0.1359', '0.7026', '-0.5464', '-0.629', '0.1678', '0.2292', '0.33', '0.713', '-0.714', '0.0631', '-0.1678', '-0.04434', '-0.4124', '-0.559', '-0.2957', '-0.2766', '0.2045', '-0.08307', '0.1902', '-0.5933', '0.5547', '-0.069', '-0.1678', '-0.0137', '-0.642', '-0.257', '0.1283', '-0.1367', '-1.046', '-0.1842', '-0.2207', '0.517', '0.571', '0.591', '0.0815', '-0.1235', '0.3071', '-0.2173', '0.1145', '0.3394', '0.321', '-0.6245', '0.3352', '-0.323', '0.04236', '0.2617', '0.2659', '-0.595', '-0.3176', '-0.171', '0.2208', '-0.4114', '0.0437', '-0.02368', '-0.4524', '-0.4673', '0.749', '-0.4802', '0.8257', '0.1993', '0.977', '0.4968', '0.2489', '-0.05267', '-0.1863', '0.2803', '0.4421', '0.586', '0.4517', '0.2463', '-0.531', '0.6367', '0.5737']",,,C535396,,,,
mondo:0007168,atelosteogenesis type III,"['AO3', 'atelosteogenesis type 3', 'atelosteogenesis, type III', 'atelosteogenesis, type 3', 'Aoiii', 'AOIII']",,108721,56305,,"['-0.4468', '0.2367', '-0.0998', '-0.03638', '0.3289', '-0.5005', '-0.1603', '0.6543', '-0.3025', '-0.41', '-0.3794', '-0.04398', '-0.098', '0.0973', '0.1927', '0.5376', '0.1797', '-0.1897', '-0.3633', '-0.2125', '-0.00809', '0.2297', '0.7827', '0.1025', '0.3123', '0.03574', '-0.2615', '0.2542', '0.4236', '-0.3894', '0.0661', '-0.0248', '0.732', '0.2983', '0.2285', '-0.538', '0.2073', '-0.3977', '-0.3115', '-0.237', '-0.2556', '-0.1802', '-0.0858', '0.4636', '0.05713', '-0.1361', '-0.451', '0.2896', '-0.1191', '-0.016', '-0.1318', '-0.3862', '-0.5493', '0.3535', '0.0761', '-0.588', '-0.09546', '-0.3613', '0.2212', '0.3108', '0.01524', '0.0894', '-0.3672', '0.3376', '-0.2125', '-0.1316', '-0.1935', '0.4988', '-0.5596', '0.11084', '-0.2983', '0.0831', '0.2152', '-0.04877', '-0.1302', '0.1609', '-0.26', '0.0659', '-0.4675', '-0.1293', '0.2947', '-0.01009', '0.2244', '0.232', '-0.2927', '0.7173', '0.1688', '0.602', '0.689', '-0.126', '-0.2827', '0.3374', '-0.3945', '0.11145', '0.7144', '0.561', '0.5107', '-0.503', '0.5244', '0.2795']",,,C579928,,,,
mondo:0007169,atherosclerosis susceptibility,"['ATHS', 'atherosclerosis, susceptibility to', 'Atherogenic lipoprotein phenotype', 'atherosclerosis susceptibility']",,108725,,,,,,,,,,
mondo:0007170,atresia of external auditory canal and conductive deafness,['atresia of external auditory canal and conductive deafness'],,108760,,C3276095,,,,,,,,
mondo:0007171,atrial standstill 1,"['atrial standstill caused by mutation in GJA5', 'atrial standstill type 1', 'atrial standstill 1', 'atrial cardiomyopathy with heart block', 'GJA5 atrial standstill', 'atrial standstill, digenic (GJA5/SCN5A)', 'cardiomyopathy, familial, with conduction disturbance', 'ATRST1']",0080662,108770,,,,,,,,,,
mondo:0007172,atrial septal defect 1,"['ASD 2', 'ASD 1', 'atrial septal defect, secundum type', 'atrial septal defect 1', 'atrial septal defect, primum type', 'ASD1', 'atrial heart septal defect type 1']",0110106,108800,,C1862389,,,,,,,,
mondo:0007173,atrial septal defect 7,"['ASD with or without atrioventricular conduction defects', 'NKX2-5 atrial heart septal defect', 'atrial heart septal defect caused by mutation in NKX2-5', 'atrial septal defect 7 with or without atrioventricular conduction defects', 'ASD7', 'atrial septal defect 7, with or without AV conduction defects', 'atrial heart septal defect type 7', 'atrial septal defect-atrioventricular conduction defects syndrome']",0110112,108900,1479,C3502353,"['-0.2078', '-0.003048', '0.2313', '-0.04794', '0.3972', '-0.2245', '0.5347', '0.478', '-0.3027', '0.06635', '-0.549', '-0.615', '-0.1316', '0.2993', '-0.382', '-0.1913', '-0.677', '-0.01845', '-0.3936', '-0.4172', '-0.03207', '0.713', '0.587', '-0.02846', '0.5273', '-0.3547', '0.3623', '0.3862', '0.3918', '0.2048', '0.4155', '0.4148', '0.5024', '0.2817', '0.209', '-0.4524', '0.2294', '-0.0584', '0.2333', '-0.9014', '0.3115', '-0.1484', '0.1862', '0.08026', '0.05646', '-0.11127', '0.11487', '0.5015', '-0.2118', '0.1041', '0.1355', '-0.369', '-0.1705', '-0.2988', '-0.634', '-0.4436', '-0.21', '0.4158', '-0.508', '-0.1559', '-0.2094', '0.2808', '0.4565', '0.2355', '-0.343', '-0.2413', '0.6094', '0.3552', '-0.435', '0.1134', '-0.07336', '-0.08746', '0.09326', '-0.05142', '-0.0428', '-0.195', '0.00622', '0.06335', '-0.792', '-0.34', '-0.00936', '0.1628', '0.3506', '0.09686', '0.2327', '-0.4644', '0.526', '0.2372', '-0.1353', '-0.1321', '-0.11597', '0.175', '0.3103', '0.2886', '0.9053', '0.274', '0.738', '-0.5356', '-0.632', '0.1556']",,,,,,,
mondo:0007174,Lown-Ganong-Levine syndrome,"['syndrome of short P-R interval, normal QRS complexes, and supraventricular tachycardias', 'Lown-Ganong-Levine syndrome', 'atrial tachyarrhythmia with short PR interval', 'LGL syndrome']",13087,108950,844,C1862387,,,,D008151,426.81,,10024984,
mondo:0007175,"PR interval, variation in","['PR interval, variation in', 'Atrioventricular conduction time, variation in', 'PR interval, variation type in']",,108980,,C3152251,,,,,,,,
mondo:0007176,helicoid peripapillary chorioretinal degeneration,"['Sveinsson chorioretinal atrophy', 'peripapillary chorioretinal Degeneration, Icelandic type', 'atrophia areata', 'SVEINSSON chorioretinal atrophy', 'SCRA', 'helicoidal peripapillary chorioretinal Degeneration']",0111228,108985,86813,C1862382,"['-0.6543', '0.0762', '-0.2008', '0.1954', '0.262', '-0.5615', '-0.3696', '0.357', '-0.5684', '-0.3357', '-0.0503', '-0.09515', '-0.2262', '-0.209', '0.011635', '-0.07666', '0.0631', '-0.4219', '-0.1114', '-0.7573', '0.0794', '-0.3584', '-0.1866', '0.07434', '0.2367', '0.3218', '-0.54', '-0.05084', '-0.10406', '0.5537', '0.4968', '0.0906', '-0.2905', '0.3013', '0.02068', '0.00916', '0.1079', '-0.0687', '-0.01764', '-0.0849', '0.1603', '-0.0922', '0.2314', '0.2418', '-0.1306', '-0.1836', '0.0971', '-0.02547', '0.366', '0.0734', '0.422', '0.0944', '-0.05176', '-0.2357', '0.1262', '-0.4785', '0.9326', '-0.003597', '-0.5312', '0.1868', '0.0991', '0.06757', '-0.0991', '0.436', '-0.2023', '0.4517', '0.651', '0.888', '-0.01657', '0.618', '-0.382', '0.2499', '0.08466', '0.01322', '0.2191', '-0.5337', '0.184', '0.4717', '-0.3264', '-0.1888', '0.1892', '-0.1173', '0.06775', '0.749', '-0.4172', '-0.723', '0.2786', '0.2476', '0.1388', '0.4229', '0.205', '0.2446', '0.2479', '0.02475', '0.488', '-0.0894', '0.607', '-0.0993', '0.0177', '0.1735']",,,C566236,,,,
mondo:0007177,auriculoosteodysplasia,"['auriculo-osteodysplasia', 'auriculoosteodysplasia', 'multiple osseous dysplasia, characteristic ear shape, and short stature']",,109000,114,C1862381,,,,C538271,,,,
mondo:0007178,aurocephalosyndactyly,"['aurocephalosyndactyly', 'aural cephalosyndactyly', 'Kurczynski-Casperson syndrome', 'Auralcephalosyndactyly']",,109050,1219,C1862380,,,,C566235,,,,
mondo:0007179,autoimmune disease,"['autoimmune hypersensitivity disease', 'disease, autoimmune', 'autoimmune disorder', 'autoimmune disease', 'hypersensitivity reaction type II disease']",417,109100,,C0004364,"['-0.2688', '0.191', '-0.01884', '-0.1304', '-0.011665', '-0.01585', '0.1788', '-0.576', '-0.1831', '-0.09845', '0.005245', '-0.11035', '-0.0642', '0.1555', '-0.2317', '-0.172', '-0.1274', '0.02309', '-0.1897', '-0.6206', '0.0056', '-0.4517', '0.512', '-0.326', '0.1653', '-0.179', '-0.10474', '-0.001127', '-0.219', '-0.2119', '0.3516', '0.2455', '0.425', '0.112', '0.1454', '-0.1118', '-0.3486', '0.206', '0.03262', '-0.2404', '0.228', '0.012886', '-0.001174', '-0.3108', '0.2722', '-0.382', '0.1522', '-0.0864', '0.384', '0.3296', '-0.1145', '0.2476', '0.399', '0.2668', '-0.1885', '0.08673', '0.1663', '-0.10596', '-0.5093', '0.0327', '0.2146', '0.0974', '-0.10614', '0.1925', '-0.0666', '0.1495', '0.3835', '0.3179', '-0.3232', '0.24', '-0.1686', '-0.10205', '-0.128', '-0.1433', '0.05194', '0.03784', '0.01955', '0.4104', '-0.1382', '-0.3967', '-0.319', '-0.1617', '0.1276', '-0.008316', '-0.3884', '-0.3252', '-0.00728', '-0.0516', '-0.003416', '-7.16e-05', '0.3372', '0.1273', '-0.05115', '-0.252', '0.27', '0.3445', '0.1318', '-0.0578', '-0.2036', '0.4246']",C2889,0005140,D001327,720,,,
mondo:0007180,"Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities","['iris dysplasia with ocular hypertelorism, psychomotor retardation, and sensorineural deafness', 'De Hauwere syndrome', 'Axenfeld-Rieger anomaly with partially absent eye muscles, distinctive face, hydrocephaly, and skeletal abnormalities']",,109120,1831,C1862373,,,,C566234,,,,
mondo:0007181,axial osteomalacia,"['axial osteomalacia', 'atypical osteomalacia involving the axial skeleton']",0080039,109130,,C1862372,,,,C537791,,,,
mondo:0007182,Machado-Joseph disease,"['Azorean neurologic disease', 'Azorean disease of the nervous system', 'Machado disease', 'Machado-Joseph disease', 'spinocerebellar ataxia 3', 'spinocerebellar atrophy type 3', 'Nigro-spino-dentatal degeneration with nuclear ophthalmoplegia', 'MJD', 'SCA3', 'spinocerebellar ataxia type 3', 'Nigrospinodentatal Degeneration', 'autosomal dominant striatonigral degeneration', 'spinocerebellar atrophy 3', 'Spinopontine atrophy', 'Azorean disease']",1440,109150,98757,C0024408,"['-0.00887', '0.05225', '0.003363', '-0.0092', '0.001697', '-0.07495', '0.007095', '0.03503', '-0.03778', '-0.01546', '-0.01857', '-0.01414', '-0.01762', '0.008125', '0.01218', '-0.02034', '0.0004582', '-0.01318', '-0.0006976', '-0.09644', '0.014114', '-0.03084', '0.04068', '-0.01519', '0.01732', '-0.0137', '-0.006184', '-0.011665', '-0.003233', '-0.0243', '0.02766', '0.02762', '0.04117', '0.02406', '0.02405', '-0.03137', '-0.01376', '-0.01822', '-0.00966', '-0.03156', '0.00891', '-0.06885', '0.02452', '-0.004936', '0.005917', '-0.04224', '-0.02362', '0.03116', '0.02571', '0.01419', '-0.004196', '-0.01942', '-0.001775', '-0.01744', '-0.02478', '-0.01521', '0.05447', '-0.012115', '-0.05576', '0.001027', '0.01678', '0.0283', '0.01617', '-0.005054', '0.010445', '0.01516', '0.05347', '0.01475', '-0.02869', '0.05215', '-0.03323', '-0.006123', '0.0212', '-0.02853', '0.0341', '0.02777', '-0.00847', '-0.01484', '-0.0385', '-0.01837', '0.001293', '-0.01166', '-0.02629', '0.04947', '-0.01006', '-0.01103', '0.02237', '0.05005', '0.0569', '0.02788', '0.022', '0.04', '0.015045', '0.02214', '0.0939', '0.03317', '0.0449', '-0.04926', '-0.02032', '-0.01215']",C84830,,D017827,336.8,,,
mondo:0007183,"azotemia, familial","['azotemia, familial']",,109160,,C1862358,,,,C566233,,,,
mondo:0007184,"alopecia, androgenetic, 1","['baldness, Male pattern', 'AGA1', 'alopecia, androgenetic, 1']",,109200,,,,,,,,,,
mondo:0007185,Banki syndrome,"['fusion of the lunate and cuneiform bones of the wrist, clinodactyly, clinometacarpy, brachymetacarpy and leptometacarpy (thin diaphysis)', 'Banki syndrome']",,109300,1228,C1862319,,,,C566228,,,,
mondo:0007186,gastroesophageal reflux disease,"['GERD', 'GERD - gastro-esophageal reflux disease', 'gastro-esophageal reflux', 'Gastresophageal reflux', 'acid reflux', 'gastroesophageal reflux', 'ger', 'gastroesophageal reflux disease', 'gastroesophageal reflux, paediatric', 'gastroesophageal reflux, pediatric']",8534,109350,,C0017168,,C26781,0003948,D005764,530.81,,,
mondo:0007187,nevoid basal cell carcinoma syndrome,"['NBCCS', 'nevoid basal cell carcinoma syndrome', 'basal cell nevus syndrome', 'BCNS', 'Gorlin syndrome', 'multiple basal cell nevi, odontogenic keratocysts, and skeletal anomalies', 'multiple basal cell carcinomas', 'nevoid basal cell cancer syndrome', 'Gorlin-Goltz syndrome']",2512,109400,377,C0004779,"['0.09204', '-0.06696', '-0.4595', '0.4883', '0.325', '-0.1665', '0.551', '0.9087', '-0.2374', '-0.293', '0.8726', '0.402', '0.0814', '0.3684', '-1.441', '-0.568', '0.2117', '-0.56', '0.02402', '-0.12225', '-0.624', '-0.3408', '-0.1592', '-0.5615', '0.01371', '-0.3904', '-0.637', '-0.474', '-0.1345', '-0.309', '0.5073', '-0.1932', '0.5386', '-0.2035', '0.3975', '0.331', '-0.2108', '-0.2693', '0.2141', '-0.332', '0.518', '-0.1356', '-0.07336', '0.11346', '0.2842', '-0.509', '-0.1893', '-0.584', '0.04984', '-0.6387', '0.482', '-0.4397', '0.466', '-0.1709', '-0.5454', '-0.2437', '-0.1196', '0.434', '-0.3142', '-0.09393', '-0.1708', '-0.04636', '-0.722', '0.276', '0.1837', '0.6807', '0.4995', '0.7656', '0.4429', '1.173', '0.1627', '0.143', '0.2263', '-0.002771', '0.2979', '0.547', '-0.7817', '-0.3008', '-0.0951', '-0.75', '-0.418', '-0.0395', '0.04645', '-0.2336', '-0.52', '-0.5464', '0.0862', '0.6396', '0.2052', '0.176', '0.1826', '0.2318', '-0.3538', '0.0769', '0.2727', '-0.12366', '0.04376', '-0.679', '-0.0529', '-0.06274']",C2892,,D001478,,,10062804,
mondo:0007188,primary basilar invagination,"['primary basilar impression', 'basilar impression, primary', 'Bull-Nixon syndrome']",,109500,2285,C1862299,,,,C566226,,,,
mondo:0007190,"leukemia, chronic lymphocytic, susceptibility to, 2","['Clls2', 'leukemia, chronic lymphocytic, susceptibility to, 2', 'leukemia, chronic lymphocytic, susceptibility to, type 2', 'leukemia, chronic lymphocytic, B-cell', 'disrupted in B-cell malignancy', 'B-cell malignancy, low-grade']",,109543,,,,,,,,,,
mondo:0007191,Behcet disease,"['triple symptom complex', 'Behcet^s syndrome', 'Behcet disease', 'Behçet disease', 'silk road disease', 'Adamantiades-Behcet disease', 'Behçet’s disease', 'Behçet^s syndrome', 'Morbus Behçet^s syndrome', 'BD', 'Behcet syndrome', 'Behet^s syndrome', 'Behçet syndrome', 'Behçet^s disease', 'Behçet-Adamantiades syndrome', 'Behcet^s disease']",13241,109650,117,C0004943,,C34416,0003780,D001528,136.1,,10004213,
mondo:0007192,"beta-amino acids, renal transport of","['taurine renal reabsorption', 'AABT', 'BETA-amino acids, renal TRANSPORT OF']",,109660,,C1862289,,,,,,,,
mondo:0007193,primary biliary cholangitis 1,"['Pbc', 'biliary cirrhosis, primary, 1', 'PBC1']",0070358,109720,,CN029380,,,,,,,,
mondo:0007194,familial bicuspid aortic valve,"['familial BAV', 'aortic valve disease type 1', 'AOVD1', 'aortic valve disease 1']",0080332,,402075,C0428791,"['-0.0824', '-0.05325', '0.08856', '-0.1888', '0.2126', '-0.252', '0.1663', '0.566', '-0.3274', '0.02287', '-0.1948', '-0.3367', '-0.01593', '0.0604', '-0.2311', '-0.368', '-0.3884', '-0.1132', '-0.1652', '-0.5674', '0.1372', '0.2112', '0.5166', '-0.04874', '0.0924', '0.1005', '0.3362', '0.1594', '0.3613', '-0.093', '0.5635', '0.0127', '0.404', '0.3208', '-0.08936', '-0.3452', '0.1772', '0.1938', '0.3076', '-0.473', '0.4001', '0.08575', '0.4268', '0.07086', '-0.0583', '0.1671', '-0.165', '0.4214', '-0.197', '0.08044', '-0.0958', '0.10175', '0.1219', '-0.209', '-0.1099', '-0.2236', '0.2964', '-0.1725', '-0.255', '-0.205', '0.307', '0.636', '0.04193', '-0.1389', '0.2114', '-0.09296', '0.5522', '0.1648', '-0.5557', '0.2654', '-0.2365', '0.0231', '0.1978', '-0.169', '-0.1346', '-0.288', '-0.005714', '0.2261', '-0.531', '-0.2188', '-0.229', '0.2249', '0.08655', '-0.09796', '-0.06287', '-0.0454', '0.3245', '0.01263', '-0.13', '-0.3718', '0.1454', '0.1257', '0.10175', '0.3823', '0.7056', '-0.2296', '0.644', '-0.2314', '-0.3948', '0.02417']",,,,,,,
mondo:0007195,"bifid nose, autosomal dominant","['bifid nose, autosomal dominant']",,109740,,C2751431,,,,,,,,
mondo:0007197,bladder diverticulum,"['bladder diverticulum', 'bladder diverticulum (disease)', 'diverticulum - bladder', 'diverticulum of bladder']",11353,109820,,,,C160155,,C562406,596.3,N32.3,,0000015
mondo:0007198,Ascher syndrome,"['Double upper lip, blepharochalasis and enlargement of the thyroid', 'blepharochalasis-double lip syndrome', 'Ascher syndrome', 'blepharochalasis and DOUBLE LIP', 'blepharochalasis and Double lip', 'blepharochalasis and double lip', 'Ascher^s syndrome', 'blepharochalasis and Double type lip', 'blepharochalasis - double lip']",,109900,1253,C0339085,,,,C562742,374.89,,,
mondo:0007199,"blepharochalasis, superior","['blepharochalasis, superior']",,110000,,C1862275,,,,C566223,,,,
mondo:0007200,blepharonasofacial malformation syndrome,"['blepharonasofacial malformation syndrome', 'Pashayan-Prozansky syndrome', 'Pashayan syndrome']",,110050,1252,C0796197,,,,C536303,,,,
mondo:0007201,"blepharophimosis, ptosis, and epicanthus inversus syndrome","['blepharophimosis-epicanthus inversus-ptosis syndrome', 'BPES with ovarian failure', 'blepharophimosis, ptosis, and epicanthus inversus syndrome type 1', 'blepharophimosis, epicanthus inversus, and ptosis, type 2', 'BPES', 'BPES with premature ovarian failure', 'blepharophimosis syndrome type 1', 'BPES with Duane retraction syndrome', 'blepharophimosis, ptosis, and epicanthus inversus', 'blepharophimosis, ptosis, epicanthus inversus syndrome', 'BPES, type 1', 'BPES, type I, autosomal recessive', 'blepharophimosis, epicanthus inversus, and ptosis, type 1', 'blepharophimosis types 1 and 2', 'BPES, type 2', 'blepharophimosis, ptosis, epicanthus inversus with ovarian failure', 'BPES type 1', 'BPES without ovarian failure']",14778,110100,126,C0220663,"['0.397', '-0.1257', '-0.3022', '-0.2847', '-0.06155', '-0.2363', '0.276', '0.1697', '-1.062', '-0.213', '0.1838', '-0.01254', '0.4412', '0.2322', '-0.3938', '-0.3533', '0.3347', '-0.2644', '0.05545', '-0.5234', '-0.868', '-0.3933', '0.6772', '-0.8457', '0.1137', '0.1605', '-0.01799', '-0.05582', '1.038', '-0.06586', '0.836', '0.622', '0.894', '-0.582', '-0.1815', '-0.355', '0.02522', '-0.2368', '-0.1698', '-0.502', '0.6904', '0.2532', '0.2072', '0.2925', '0.2341', '-0.5444', '-0.02269', '0.3928', '-0.467', '0.001541', '-0.1744', '-0.1375', '0.04587', '-0.1617', '-0.2076', '-0.419', '0.573', '-0.06305', '-0.518', '0.4775', '0.5864', '0.1515', '0.6006', '0.6997', '-0.0958', '-0.1335', '0.3218', '0.0715', '0.2299', '0.3677', '-0.3337', '0.2183', '0.3906', '-0.578', '0.1362', '-0.329', '-0.005177', '-0.3032', '-0.8037', '0.11084', '0.9854', '-0.09485', '-0.152', '0.2062', '-0.52', '-0.1443', '0.1148', '-0.04736', '0.1495', '-0.0623', '-0.3462', '0.3762', '0.1997', '0.611', '0.5596', '-0.5425', '0.5117', '-0.1525', '0.1504', '0.1329']",,,C562419,,,,
mondo:0007202,blepharoptosis-myopia-ectopia lentis syndrome,"['blepharoptosis myopia ectopia lentis', 'dominantly inherited blepharoptosis, high myopia, and ectopia lentis', 'blepharoptosis, myopia, and ectopia lentis']",,110150,1259,C1862259,,,,C536236,,,,
mondo:0007203,blue rubber bleb nevus,"['bean syndrome', 'blue rubber bleb nevus', 'blue rubber bleb nevus syndrome', 'BRBN', 'BRBNS']",,112200,1059,C0346072,,C4486,,C536240,,,,
mondo:0007204,Cole-Carpenter syndrome 1,"['Cole-Carpenter syndrome caused by mutation in P4HB', 'Cole-Carpenter syndrome type 1', 'COLE-CARPENTER syndrome 1', 'Cole-Carpenter syndrome 1', 'bone fragility with craniosynostosis, ocular proptosis, hydrocephalus, and distinctive Facial features', 'P4HB Cole-Carpenter syndrome', 'CLCRP1']",,112240,,CN029402,,,,,,,,
mondo:0007205,diaphyseal medullary stenosis-bone malignancy syndrome,"['bone dysplasia-medullary fibrosarcoma syndrome', 'diaphyseal medullary stenosis with malignant fibrous histiocytoma', 'diaphyseal medullary stenosis-malignant fibrous histiocytoma syndrome', 'BDMF', 'DMS-MFH', 'Hardcastle syndrome', 'myopathy, limb-girdle, with bone fragility', 'bone dysplasia with malignant fibrous histiocytoma', 'Hardcastle^s syndrome', 'bone dysplasia with medullary fibrosarcoma', 'DMSMFH']",0080664,112250,85182,C1862177,"['-0.1593', '0.05164', '0.4219', '-0.677', '0.2893', '-0.1195', '0.1412', '0.6216', '-0.1334', '-0.07025', '-0.2944', '0.04898', '4.435e-05', '-0.2964', '-0.1718', '0.01445', '0.1926', '-0.07306', '0.0455', '-0.519', '0.010994', '-0.2239', '0.4678', '-0.3086', '0.0724', '0.1624', '0.06757', '-0.0459', '-0.03436', '-0.3472', '0.2273', '-0.05563', '0.212', '0.02774', '-0.01149', '-0.1609', '-0.115', '-0.2318', '-0.02696', '-0.584', '0.19', '-0.1193', '0.5044', '-0.4026', '0.01386', '-0.4236', '-0.1294', '0.2063', '0.3918', '-0.1646', '0.3635', '-0.01926', '0.01512', '0.12384', '-0.2878', '-0.685', '-0.2256', '0.01563', '-0.392', '-0.02765', '0.6064', '0.0715', '-0.3335', '-0.39', '-0.05017', '0.1693', '0.3977', '0.436', '-0.2917', '0.483', '-0.0641', '-0.2134', '0.2373', '-0.1805', '-0.01814', '-0.1122', '-0.2656', '0.1934', '-0.09064', '-0.432', '-0.3813', '0.1696', '-0.0841', '0.3179', '-0.699', '-0.10645', '0.2896', '0.10284', '-0.0857', '-0.0897', '-0.1417', '0.0906', '-0.1225', '0.0664', '0.5244', '0.1296', '0.6895', '-0.2422', '-0.01604', '-0.10486']",C122660,,,,,,
mondo:0007206,"bone pain, periodic","['bone pain, periodic']",,112270,,,,,,,,,,
mondo:0007207,Böök syndrome,"['PHC syndrome', 'Böök syndrome', 'premolar aplasia, hyperhidrosis, and canities prematura', 'book syndrome']",,112300,1262,C0457014,,,,C562993,,,,
mondo:0007208,Boomerang dysplasia,"['Boomerang-like skeletal dysplasia', 'dwarfism with short, bowed, rigid limbs and characteristic facies', 'Boomerang dysplasia']",0050680,112310,1263,C0432201,"['-0.3782', '0.4482', '0.0825', '0.003105', '0.2625', '-0.381', '-0.1975', '0.81', '-0.3335', '-0.5103', '-0.09674', '-0.05618', '-0.0881', '0.1522', '-0.3452', '0.2712', '0.4429', '-0.2291', '-0.441', '-0.638', '0.00537', '0.08453', '1.005', '0.04474', '0.1722', '-0.0667', '-0.1405', '-0.01229', '0.579', '-0.2091', '-0.3335', '-0.2145', '0.12244', '0.6064', '0.4', '-0.2776', '-0.07275', '-0.4531', '-0.0741', '-0.1072', '-0.2334', '-0.2499', '-0.00817', '-0.151', '-0.1749', '0.004795', '-0.3818', '0.4565', '0.1245', '-0.126', '0.1385', '-0.4287', '0.0887', '-0.0973', '-0.3708', '-0.682', '-0.2007', '-0.3926', '0.235', '0.1926', '0.582', '0.1294', '-0.634', '0.331', '-0.263', '-0.2864', '0.1447', '0.437', '-0.2583', '0.35', '-0.02649', '0.05862', '0.2683', '-0.2051', '-0.391', '0.1068', '-0.006367', '-0.0415', '-0.3967', '-0.242', '-0.3147', '-0.04144', '0.01508', '0.4', '-0.2253', '0.4927', '-0.02525', '0.2598', '0.331', '-0.1332', '0.1105', '-0.02954', '0.1764', '0.263', '0.3608', '0.5073', '0.4219', '-0.4006', '0.516', '0.3523']",,,C536573,756.9,,,
mondo:0007209,Weismann-Netter syndrome,"['Weismann-Netter syndrome', 'anterior bowing of legs with dwarfism', 'bowing of legs, anterior, with dwarfism', 'WEISMANN-NETTER syndrome', 'Weismann Netter syndrome', 'WNS', 'Weismann-Netter-Stuhl syndrome', 'Toxopachyosteose Diaphysaire Tibio-Peroniere', 'bowing of legs, anterior with dwarfism']",,112350,3344,C1862172,,,,C537082,,,,
mondo:0007210,"Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay","['Brachmann-de Lange-like facial changes with microcephaly, metatarsus adductus, and developmental delay']",,112370,,C1862171,,,,C566206,,,,
mondo:0007211,brachydactyly-arterial hypertension syndrome,"['brachydactyly type E, with short stature and hypertension', 'brachydactyly type E with short stature and hypertension', 'HTNB', 'hypertension and brachydactyly syndrome', 'Bilginturan brachydactyly', 'brachydactyly, type E, with short stature and hypertension', 'Bilginturan syndrome', 'brachydactyly with hypertension']",0111247,112410,1276,C1862170,"['0.01236', '-0.07806', '-0.3481', '0.3457', '0.168', '-0.9497', '0.1606', '0.5513', '-0.493', '-0.1981', '0.1978', '0.362', '0.1699', '0.4578', '-0.1186', '-0.6504', '0.424', '0.03857', '0.377', '-0.486', '0.069', '0.135', '0.4792', '-0.201', '-0.03375', '0.2925', '-0.0268', '0.11237', '0.7983', '-0.213', '0.7036', '-0.3674', '0.6846', '0.1969', '0.6396', '0.11743', '-0.2905', '-0.654', '0.12256', '-0.3054', '0.1127', '-0.4778', '0.382', '-0.375', '-0.01495', '0.0653', '0.0922', '0.77', '0.2194', '-0.2708', '0.6226', '0.4526', '0.2363', '-0.51', '-0.5015', '-0.5625', '-0.649', '-0.5713', '0.2239', '0.2166', '-0.007168', '0.4175', '-0.05038', '-0.976', '-0.3428', '0.5796', '-0.1305', '0.741', '-0.559', '0.2148', '0.01807', '0.5522', '0.2947', '-0.415', '-0.279', '-0.249', '-0.3562', '-0.2117', '0.014244', '0.08014', '-0.0166', '0.542', '-0.2449', '0.06174', '0.1902', '0.159', '0.2114', '-0.216', '1.159', '-0.2605', '0.2551', '0.586', '-0.3972', '0.03647', '0.5664', '0.0883', '-0.03876', '-0.02338', '0.2864', '0.327']",,,C537095,,,,
mondo:0007212,brachydactyly-long thumb syndrome,"['brachydactyly long thumb type', 'brachydactyly, long thumb type', 'long-thumb brachydactyly syndrome', 'brachydactyly, long-thumb type']",,112430,2946,C1862169,,,,C566204,,,,
mondo:0007213,Ballard syndrome,"['Pitt-Williams brachydactyly', 'brachydactyly, combined B and E types', 'brachydactyly, Ballard type', 'Ballard type brachydactyly', 'Pitt Williams brachydactyly', 'brachydactyly types B and E combined', 'brachydactyly Ballard type', 'brachydactyly combined B and E types']",0110963,112440,93395,C1862163,,,,C537094,,,,
mondo:0007214,brachydactyly-preaxial hallux varus syndrome,"['Christian brachydactyly', 'preaxial brachydactyly with hallux varus and thumb abduction', 'dominant preaxial brachydactyly with hallux varus and thumb abduction', 'brachydactyly preaxial with hallux varus and thumb abduction', 'brachydactyly, preaxial, with hallux varus and thumb abduction']",0110962,112450,1278,C1862162,,,,C537087,,,,
mondo:0007215,brachydactyly type A1,"['brachydactyly, type A1', 'Farabee-type brachydactyly', 'brachydactyly Farabee type', 'brachydactyly, Farabee type', 'BDA1', 'Farabee type brachydactyly']",0110964,112500,93388,C1862151,"['-0.3574', '-0.1937', '0.1687', '-0.3354', '0.2651', '-0.3694', '-0.2546', '0.662', '-0.2751', '-0.5874', '-0.1317', '0.0848', '-0.2451', '0.05273', '-0.0745', '0.0953', '0.05206', '-0.2783', '-0.3345', '-0.5117', '-0.02628', '0.3584', '0.595', '0.03035', '0.5117', '0.3076', '0.06915', '0.06366', '0.1891', '-0.0985', '0.255', '-0.507', '0.02733', '0.1931', '0.1993', '-0.2269', '-0.01872', '-0.07184', '0.01151', '-0.1508', '-0.176', '-0.3013', '0.1777', '-0.0734', '0.0666', '-0.451', '-0.3289', '0.8027', '0.2935', '-0.07306', '0.1888', '-0.1164', '-0.06586', '0.04263', '-0.3677', '-0.6455', '-0.035', '-0.0655', '-0.3003', '-0.005367', '-0.061', '-0.07135', '0.1123', '-0.05472', '-0.5054', '-0.11194', '0.2448', '0.3499', '-0.1942', '0.08405', '-0.534', '0.1852', '0.3806', '-0.4177', '0.552', '0.2491', '-0.2695', '-0.2678', '-0.3835', '-0.27', '-0.0905', '0.1295', '0.2751', '0.1638', '0.1758', '0.08325', '-0.332', '0.299', '0.1891', '-0.4258', '-0.3635', '0.3965', '0.2273', '0.1504', '0.4417', '-0.2832', '0.1885', '-0.637', '0.452', '0.242']",,,C537088,,,,
mondo:0007216,brachydactyly type A2,"['Mohr-Wriedt type brachydactyly', 'brachydactyly, type A2', 'BDA2', 'Brachymesophalangy type 2', 'brachymesophalangy II', 'Brachymesophalangy 2', 'brachydactyly, Mohr-Wriedt type']",0110965,112600,93396,,"['-0.4338', '-0.2186', '-0.2964', '-0.0986', '0.4565', '-0.5884', '-0.2837', '0.6475', '-0.762', '-1.0625', '-0.262', '0.1349', '-0.015564', '0.0935', '-0.0911', '0.04654', '0.3079', '-0.355', '-0.2712', '-0.2766', '0.1512', '0.2795', '0.4307', '-0.2988', '0.5933', '0.3047', '-0.3896', '-0.0798', '0.3567', '0.1313', '0.557', '-0.617', '-0.05957', '-0.03427', '0.3772', '-0.2537', '0.4727', '-0.3208', '0.0631', '-0.3838', '-0.1593', '-0.2969', '-0.1481', '-0.1045', '-0.1699', '-0.065', '-0.1243', '0.673', '0.3398', '-0.11444', '0.0166', '-0.331', '-0.11804', '0.319', '-0.7236', '-0.1105', '0.2644', '-0.04257', '-0.2029', '0.2438', '-0.06775', '-0.0448', '0.04654', '0.0516', '-0.4436', '-0.04852', '0.02113', '0.2666', '-0.2688', '-0.0723', '-0.614', '0.4824', '0.278', '-0.04297', '0.525', '0.2986', '0.0561', '-0.05325', '-0.523', '-0.3855', '-0.10144', '-0.2012', '0.69', '0.2339', '0.2947', '0.02196', '-0.4004', '0.547', '0.3555', '0.02419', '-0.1078', '0.3513', '0.3298', '0.0748', '0.4084', '-0.3628', '0.4854', '-1.25', '0.2349', '0.327']",,,C537089,,,,
mondo:0007217,brachydactyly type A3,"['brachydactyly-clinodactyly', 'Brachymesophalangy 5', 'BDA3', 'brachymesophalangy V', 'brachydactyly, type A3']",0110966,112700,93393,C1862140,,,,C537090,,,,
mondo:0007218,brachydactyly type A4,"['brachydactyly, Temtamy type', 'Brachymesophalangy 2 and 5', 'Brachymesophalangy II and V', 'brachydactyly Temtamy type', 'brachymesophalangy II and V', 'BDA4', 'Temtamy type brachydactyly', 'brachydactyly, type A4']",0110967,112800,93394,,,,,C537097,,,,
mondo:0007219,Osebold-Remondini syndrome,"['brachydactyly, type A6', 'BDA6', 'brachydactyly type A6', 'OSEBOLD-Remondini syndrome', 'brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities', 'Brachymesophalangy with mesomelic short limbs and carpal and tarsal osseous abnormalities', 'Osebold-Remondini syndrome']",0110968,112910,93382,C1862130,,,,C537092,,,,
mondo:0007220,brachydactyly type B1,"['BDB1', 'ROR2 brachydactyly type B', 'brachydactyly, type B', 'brachydactyly, type B1', 'brachydactyly type B caused by mutation in ROR2']",0110969,113000,572385,,,,,C566196,,,,
mondo:0007221,brachydactyly type C,"['brachydactyly, Haws type', 'brachydactyly, type C', 'brachydactyly Haws type']",0110970,113100,93384,C1862103,"['0.06696', '0.09796', '0.1687', '-0.0386', '0.1969', '-0.2773', '0.0244', '0.3806', '-0.674', '-0.2448', '-0.332', '0.2146', '0.0619', '0.0705', '-0.1271', '-0.2046', '0.1798', '-0.1914', '0.1355', '-0.2925', '-0.005424', '0.02861', '0.423', '-0.1298', '0.3245', '0.2228', '-0.05283', '0.0632', '0.08496', '-0.2052', '0.2451', '-0.2266', '0.07587', '0.1572', '0.247', '-0.2382', '-0.10925', '-0.2096', '-0.08527', '-0.1456', '0.0435', '-0.5444', '0.0415', '0.07404', '-0.002321', '-0.2566', '-0.0973', '0.4329', '-0.041', '0.06384', '-0.1958', '-0.048', '-0.11053', '-0.2566', '-0.439', '-0.3794', '-0.1421', '-0.3167', '-0.1407', '-0.1246', '0.06128', '0.1769', '-0.05295', '0.12317', '-0.1445', '-0.1571', '0.23', '0.081', '-0.09186', '-0.1296', '-0.2063', '0.0705', '0.2119', '-0.1704', '0.3252', '0.07513', '-0.1265', '-0.1096', '-0.303', '-0.411', '-0.1605', '-0.0532', '0.1335', '0.2391', '0.01782', '-0.0286', '-0.2932', '0.554', '0.2861', '-0.278', '-0.0813', '0.3838', '0.3457', '-0.08435', '0.4087', '-0.1461', '0.3', '-0.5938', '0.1458', '0.04053']",,,C537093,,,,
mondo:0007222,brachydactyly type D,"['stub thumb', 'BDD', 'brachydactyly, type D']",0110971,113200,93385,,,,,C562420,,,,
mondo:0007223,brachydactyly type E1,"['brachydactyly type E caused by mutation in HOXD13', 'BDE1', 'brachydactyly, type E1', 'brachydactyly, type E', 'HOXD13 brachydactyly type E']",0110972,113300,,,,,,C566194,,,,
mondo:0007224,"brachydactyly, type E, with atrial septal defect, type 2","['brachydactyly, type E, with atrial septal defect, type II']",,113301,,C1862101,,,,C566193,,,,
mondo:0007225,fibular aplasia-ectrodactyly syndrome,"['brachydactyly-ectrodactyly with fibular aplasia or hypoplasia', 'fibular aplasia ectrodactyly']",,113310,1118,C1862100,,,,C537930,,,,
mondo:0007226,brachydactyly-nystagmus-cerebellar ataxia syndrome,"['brachydactyly, nystagmus and cerebellar ataxia', 'brachydactyly - nystagmus - cerebellar ataxia', 'brachydactyly-NYSTAGMUS-cerebellar ataxia', 'Biemond syndrome', 'Biemond syndrome type 1']",,113400,1246,,,,,C566192,759.89,,,
mondo:0007227,Sillence syndrome,"['brachydactyly-distal symphalangism syndrome', 'brachydactyly-symphalangism syndrome']",,113450,3168,C1862092,,,,C537338,,,,
mondo:0007228,brachymesomelia-renal syndrome,"['brachymesomelia renal syndrome', 'brachymesomelia-renal syndrome', 'severe upper limb brachymesomelia, glomerulocystic renal dysplasia, cranial and facial abnormalities, corneal opacities']",,113470,,C1862084,,,,C537096,,,,
mondo:0007229,Brachymetatarsus 4,"['toe, fourth, short', 'Brachymetatarsus type 4', 'metatarsus IV, short', 'BRACHYMETATARSUS IV']",,113475,,,,,,,,,,
mondo:0007230,Brachymorphism-onychodysplasia-dysphalangism syndrome,"['Senior syndrome', 'bod syndrome', 'Brachymorphism-onychodysplasia-dysphalangism syndrome', 'Brachymorphism onychodysplasia dysphalangism syndrome']",,113477,1292,C1862082,,,,C536242,,,,
mondo:0007231,brachytelephalangy-dysmorphism-Kallmann syndrome,['BRACHYTELEPHALANGY with characteristic facies and Kallmann syndrome'],,113480,1295,C2931421,,,,C537101,,,,
mondo:0007232,autosomal dominant brachyolmia,"['brachyolmia, autosomal dominant', 'BCYM3', 'brachyolmia autosomal dominant', 'brachyrachia', 'brachyolmia type 3']",,113500,93304,,"['-0.714', '0.38', '-0.0727', '-0.2286', '0.4875', '-1.028', '-0.2057', '1.178', '-0.3833', '-0.4512', '0.184', '0.2057', '-0.345', '0.2246', '0.3528', '0.1925', '0.607', '-0.1569', '-0.402', '-0.7026', '0.179', '0.05212', '0.7246', '-0.2922', '-0.01808', '0.5063', '-0.1749', '-0.64', '0.2993', '-0.0261', '0.4607', '-0.77', '0.0762', '0.3928', '0.1393', '-0.3535', '-0.3093', '-0.542', '0.0913', '0.2769', '0.006187', '-0.701', '0.305', '0.45', '0.1587', '-0.06097', '-0.007294', '0.2019', '0.728', '0.3242', '0.777', '-0.1007', '-0.2905', '0.1547', '-0.012665', '-0.766', '-0.06683', '-0.4414', '0.1715', '0.08826', '0.715', '-0.1276', '-0.373', '-0.11743', '-0.1505', '0.03336', '-0.3484', '0.6934', '0.5293', '0.566', '-0.7646', '0.1951', '0.6226', '-0.404', '0.3147', '0.529', '-0.514', '0.341', '-0.8223', '0.00639', '-0.4429', '-0.2288', '0.03125', '0.2205', '0.159', '0.527', '0.04205', '-0.005943', '0.1571', '0.2156', '-0.1356', '0.1234', '-0.1252', '0.09766', '0.193', '0.3115', '0.896', '-0.3296', '0.1715', '-0.05673']",,,,,,,
mondo:0007233,second branchial cleft anomaly,"['branchial cysts', 'second branchial cleft fistula', 'branchial cleft', 'branchial cleft remnant', 'branchial cleft anomalies', 'second branchial cleft cyst']",,113600,141022,,,C104813,,,,,,
mondo:0007234,branchial myoclonus with spastic paraparesis and cerebellar ataxia,['branchial myoclonus with spastic paraparesis and cerebellar ataxia'],,113610,,C1862071,,,,C566188,,,,
mondo:0007235,branchiooculofacial syndrome,"['branchiooculofacial syndrome', 'hemangiomatous branchial clefts-Lip Pseudocleft syndrome', 'lip Pseudocleft-Hemangiomatous branchial cyst syndrome', 'branchial clefts with characteristic facies growth retardation imperforate nasolacrimal duct and premature ageing', 'branchial clefts with characteristic facies growth retardation imperforate nasolacrimal duct and premature aging', 'branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature Ageing', 'branchial clefts with characteristic facies, growth retardation, imperforate nasolacrimal duct, and premature Aging', 'BOFS', 'branchio-oculo-facial syndrome', 'BOFS syndrome', 'Bof syndrome']",0050691,113620,1297,,"['0.07196', '0.03506', '0.3687', '-0.1606', '0.655', '0.01643', '0.3064', '0.564', '-0.579', '-0.606', '-0.283', '-0.957', '0.391', '0.07715', '-0.645', '0.3438', '0.615', '-0.05432', '-0.2983', '-0.3804', '0.3296', '0.1257', '0.2228', '0.01317', '0.2522', '-0.4717', '-0.6333', '0.2937', '0.8535', '-0.1786', '0.739', '-0.2307', '-0.1722', '0.02586', '-0.0844', '-0.0891', '-0.3313', '0.1501', '-0.2017', '-0.3997', '0.2148', '-0.002193', '-0.02849', '-0.341', '0.3235', '-0.9526', '-0.213', '0.12415', '-0.523', '-0.02472', '-0.5093', '0.1814', '-0.1495', '-0.0663', '-0.796', '-0.5728', '0.193', '-0.055', '-0.1658', '-0.002123', '0.2278', '-0.01213', '-0.3892', '0.2795', '0.239', '-0.2085', '0.3381', '0.636', '-0.0873', '0.299', '-0.0798', '-0.10767', '-0.0184', '-0.1249', '0.08075', '-0.1422', '0.511', '0.0676', '-0.2664', '-0.7466', '0.3184', '0.302', '0.3794', '0.551', '-0.1917', '0.4082', '0.1266', '0.3137', '-0.1276', '0.2588', '-0.0724', '0.6304', '-0.2925', '0.682', '0.804', '-0.3997', '0.2035', '-0.03168', '0.5967', '0.4568']",,,,759.89,,,
mondo:0007236,branchiootorenal syndrome 1,"['branchiootorenal dysplasia', 'Melnick-Fraser syndrome', 'BOR1', 'branchiootorenal syndrome 1, with or without cataracts', 'branchiootorenal syndrome 1', 'branchiootorenal syndrome type 1']",0111423,113650,,,,,,,,,,
mondo:0007237,familial juvenile hypertrophy of the breast,"['virginal breast hypertrophy', 'juvenile gigantomastia', 'familial juvenile gigantomastia', 'juvenile macromastia', 'hypertrophy of the breast, juvenile', 'gigantomastia, juvenile', 'virginal mammary hypertrophy', 'JHB']",,113670,180176,CN226754,,,,C536821,,N62,,
mondo:0007238,amastia,"['amazia', 'breasts and/or nipples, aplasia or hypoplasia of, 1', 'complete absence of breasts', 'amastia', 'BNAH1', 'athelia', 'absent breasts and nipples']",,,,CN033494,,C118459,,C535565,,,,
mondo:0007239,epidermolytic ichthyosis,"['bullous ichthyosiform erythroderma', 'bullous congenital ichthyosiform erythroderma of Brock', 'bullous erythroderma Ichthyosiformis congenita of Brocq', 'BCIE', 'EHK', 'congenital bullous ichthyosiform erythroderma', 'bullous ichthyosis', 'epidermolytic hyperkeratosis', 'bullous congenital ichthyosiform erythroderma', 'bullous ichthyosiform erythroderma congenita', 'epidermolytic hyperkeratosis, late-onset', 'autosomal dominant epidermolytic ichthyosis', 'epidermolytic palmoplantar hyperkeratosis', 'epidermolytic ichthyosis', 'EI', 'ichthyosis hystrix Brocq type']",4603,113800,312,,"['0.10046', '-0.3582', '-0.6265', '-0.3293', '-0.05505', '-0.6655', '0.1562', '-0.1172', '-0.07544', '-0.7983', '0.01559', '0.013626', '-0.342', '0.2405', '-0.2903', '0.2922', '0.0845', '-1.043', '-0.1798', '-1.335', '-0.686', '0.04395', '1.016', '0.1116', '-0.0967', '0.604', '-0.6094', '0.1486', '-1.039', '-0.3696', '0.2378', '-0.1296', '-0.3704', '0.4575', '-0.2954', '0.675', '-0.33', '-0.569', '0.1678', '0.3384', '0.2379', '-0.4583', '0.01845', '0.379', '0.11847', '-0.11304', '-0.1951', '-0.1682', '0.6074', '0.0999', '-0.397', '-0.648', '0.1548', '-0.0824', '-0.1189', '0.2144', '0.5464', '0.413', '-0.2632', '-0.11597', '0.003275', '-0.01741', '-0.6597', '-0.1624', '-0.02908', '0.5186', '0.7236', '0.885', '0.037', '0.7397', '-0.2786', '-0.487', '0.2905', '0.3794', '0.1189', '0.4556', '0.04956', '-0.1416', '0.2754', '-0.4663', '-0.213', '-0.2152', '-0.5376', '0.1957', '-0.02707', '0.216', '-0.2852', '0.2954', '0.503', '0.11', '0.7007', '0.2156', '0.3538', '0.864', '0.3794', '0.2074', '0.3591', '-0.3477', '0.3696', '-0.04956']",C62569,,D017488,,,,
mondo:0007240,"progressive familial heart block, type 1A","['SCN5A progressive familial heart block', 'progressive familial heart block, type IA', 'progressive familial heart block type 1A', 'progressive familial heart block type IA', 'Lenegre^s syndrome', 'heart block, progressive familial, type 1', 'hereditary bundle branch system defect', 'heart block, progressive, type IA', 'PFHB1A', 'Cardiac conduction defect, progressive', 'Lev disease', 'progressive familial heart block caused by mutation in SCN5A', 'Lenegre-Lev disease', 'Lenegre^s disease', 'Lenegre disease', 'Cardiac conduction defect, nonprogressive', 'heart block progressive familial type 1', 'heart block, nonprogressive']",0111074,113900,,,"['-0.2472', '0.1951', '0.0709', '0.2458', '0.2974', '-0.1676', '0.1357', '0.0895', '-0.1757', '-0.1278', '-0.1482', '-0.412', '-0.05847', '0.10504', '-0.11414', '-0.411', '-0.4656', '-0.1785', '-0.206', '-0.3933', '-0.0715', '0.4353', '0.237', '-0.1366', '0.1791', '-0.1139', '0.186', '0.11475', '0.1593', '0.1571', '0.1013', '0.1675', '0.0243', '0.07666', '-0.2712', '-0.1958', '0.4526', '0.06235', '0.2229', '-0.4055', '0.2654', '0.04083', '0.3174', '-0.02948', '-0.02539', '-0.1137', '-0.2522', '0.207', '-0.2036', '0.08795', '0.213', '-0.16', '0.1447', '-0.04932', '-0.1644', '-0.2245', '0.4624', '0.346', '-0.3738', '0.01157', '-0.1093', '0.176', '0.1921', '0.1022', '-0.11', '-0.12177', '0.3088', '0.2255', '-0.321', '-0.02739', '-0.2316', '0.1322', '0.2484', '-0.3318', '0.0652', '0.1617', '0.02899', '0.09283', '-0.3552', '-0.1893', '-0.3787', '-0.04422', '0.1724', '0.1519', '0.256', '-0.118', '0.2323', '-0.11224', '0.1403', '0.1588', '-0.00514', '0.194', '-0.05643', '0.1929', '0.5024', '0.1982', '0.2377', '-0.3945', '-0.2443', '0.2847']",C126651,0004138,D002037,,,,
mondo:0007241,"bundle branch block, familial isolated complete right","['bundle branch block, familial isolated complete right']",,113950,,C0340504,,,,C562759,,,,
mondo:0007242,butyrylesterase 1,"['butyrylesterase 1', 'Butyrylesterase type 1']",,113960,,,,,,,,,,
mondo:0007243,Burkitt lymphoma,"['Burkitt^s tumour', 'Burkitt^s tumor', 'burkitt lymphoma, somatic', 'BL', 'Burkitt^s tumour or lymphoma', 'malignant lymphoma, Burkitt^s type', 'Burkitt lymphoma/leukemia', 'Burkitt^s tumor or lymphoma', 'Burkitt^s lymphoma', 'small non-cleaved cell lymphoma, Burkitt^s type', 'Burkitt lymphoma', 'small non-cleaved cell lymphoma']",8584,113970,543,C0006413,"['-0.1901', '0.4106', '-0.4292', '-0.1462', '-0.1654', '-0.1951', '0.4683', '1.333', '-0.2568', '-0.2133', '0.1244', '0.3584', '-0.5293', '0.02837', '-0.1531', '-0.04263', '-0.9233', '-0.555', '-0.6753', '0.1362', '-0.7583', '-0.0874', '0.3132', '-0.3413', '-0.102', '0.127', '-0.4326', '-0.2203', '-0.2422', '-0.4805', '0.339', '0.2778', '0.4229', '-0.2189', '0.4272', '0.1188', '-0.754', '0.4294', '-0.1697', '0.121', '-0.1744', '0.2102', '0.1826', '-0.973', '0.332', '0.1426', '-0.536', '-0.587', '0.3367', '-0.03287', '-0.04968', '0.4766', '0.01467', '0.3542', '-0.617', '-0.02426', '-0.2598', '-0.1323', '-0.4617', '-0.3438', '-0.0344', '0.0808', '-0.2693', '0.319', '-0.1422', '-0.1931', '0.3743', '0.2114', '0.3813', '1.291', '0.1137', '-0.261', '0.1321', '-0.1929', '0.27', '0.1882', '0.1426', '0.725', '0.2233', '-0.3845', '-0.694', '-0.4675', '-0.01229', '0.3157', '-0.772', '0.1305', '0.643', '-0.305', '0.2404', '-0.0956', '0.2646', '-0.1881', '-0.2297', '-0.2297', '0.753', '0.2499', '-0.3855', '-0.447', '-0.0932', '-0.2334']",C2912,0000309,D002051,200.2,,10067184,
mondo:0007244,Caffey disease,"['Caffey disease', 'cortical congenital hyperostosis', 'infantile cortical hyperostosis']",4257,114000,1310,C0020497,"['-0.06107', '0.10065', '-0.352', '-0.01499', '0.0813', '-0.261', '-0.1688', '0.9243', '-0.5205', '-0.49', '-0.3547', '0.7603', '-0.06018', '0.208', '-0.11804', '-0.0328', '0.2617', '0.1302', '0.10046', '-0.874', '0.3372', '-0.3655', '0.4995', '-0.6655', '0.0006633', '0.3171', '0.1865', '0.8706', '-0.279', '-0.2427', '0.1523', '0.2847', '-0.0277', '-0.274', '-0.04016', '0.1521', '-0.3628', '-0.7354', '0.1669', '0.1026', '0.0453', '-0.4612', '0.1581', '-0.084', '0.0382', '0.1089', '-0.192', '-0.2644', '0.634', '0.2751', '0.10583', '-0.00625', '0.4524', '0.4548', '0.3372', '-0.4321', '-0.562', '0.4148', '-0.1941', '-0.0571', '0.4543', '0.3555', '-0.7197', '-0.1896', '0.3518', '-0.2761', '0.2607', '-0.2688', '0.0584', '0.3784', '0.11316', '-0.0529', '0.1517', '-0.2085', '-0.0771', '0.01984', '0.1533', '0.4749', '-0.1896', '-0.8345', '-0.1293', '0.02791', '0.315', '-0.003227', '-0.014694', '0.604', '-0.02061', '0.5728', '0.06616', '-0.1615', '-0.074', '0.173', '0.0693', '-0.005493', '0.565', '0.5005', '0.816', '-0.5415', '0.3442', '-0.2993']",C118423,,D006958,756.59,,,
mondo:0007245,"cafe au lait spots, multiple","['multiple cafe-au-lait syndrome', 'NF6', 'cafe-au-lait spots, multiple', 'familial café-au-lait spots', 'autosomal dominant café au lait spots', 'multiple café-au-lait syndrome', 'multiple café-au-lait spots', 'neurofibromatosis type 6', 'multiple cafe-au-lait spots', 'familial cafe-au-lait spots']",,114030,2678,CN035858,,,,C537421,,,,
mondo:0007246,"calcific aortic disease with immunologic abnormalities, familial","['calcific aortic disease with immunologic abnormalities, familial']",,114065,,C1861974,,,,C566182,,,,
mondo:0007247,"basal ganglia calcification, idiopathic, childhood-onset","['cerebral calcification nonarteriosclerotic idiopathic childhood-onset', 'striopallidodentate calcinosis, bilateral, childhood-onset', 'cerebral calcification, nonarteriosclerotic, idiopathic, childhood-onset', 'idiopathic basal ganglia calcification childhood-onset', 'bilateral striopallidodentate calcinosis childhood-onset', 'basal ganglia calcification, idiopathic, childhood-onset', 'IBGC childhood onset', 'IBGC, childhood-onset']",,114100,,C1861967,,,,C536276,,,,
mondo:0007248,hereditary painful callosities,"['callosities, painful plantar', 'callosities, hereditary painful', 'Plamoplantar hyperkeratosis nummularis', 'Plamoplantar keratoderma nummularis', 'PPK nummularis', 'keratosis palmoplantaris nummularis']",,114140,79141,C1861964,,,,C566180,,,,
mondo:0007249,camptobrachydactyly,"['short foot/brachydactyly of toes, camptodactyly, brachydactyly', 'camptobrachydactyly']",,114150,1319,,,,,C537967,,,,
mondo:0007250,camptodactyly of fingers,"['CAMPD1', 'minor streblomicrodactyly, familial', 'camptodactyly 1', 'camptodactyly and knuckle pads', 'familial streblodactyly', 'crooked little finger, familial', 'streblodactyly']",,114200,295016,,,,,C567780,755.59,,,
mondo:0007251,campomelic dysplasia,"['Cmd1', 'Cmpd1/Sra1', 'acampomelic campomelic dysplasia', 'campomelic dysplasia', 'camptomelic dysplasia', 'campomelic dwarfism', 'acampomelic campomelic dysplasia with autosomal Sex reversal', 'CMPD1', 'Cmpd', 'CMD', 'campomelic dysplasia with autosomal Sex reversal']",0050463,114290,140,C1861923,"['-0.03973', '-0.02222', '0.04984', '-0.4802', '0.729', '-0.4763', '0.0824', '1.111', '-0.8057', '-1.285', '0.2625', '-0.56', '-0.07465', '0.46', '-0.02795', '-0.2214', '0.486', '-0.0484', '-0.6284', '-0.2861', '-0.2607', '0.3184', '0.7363', '-0.2698', '0.05', '-0.2166', '0.227', '0.053', '0.3074', '-0.6646', '0.305', '-0.1076', '0.2133', '-0.1126', '-0.04715', '-0.3953', '0.1251', '-0.5967', '-0.3904', '-0.0539', '0.3518', '-0.2133', '0.10236', '0.02083', '-0.1744', '-0.311', '-0.662', '-0.0577', '-0.1256', '0.1362', '-0.06604', '-0.2113', '-0.1631', '0.343', '-0.04382', '-0.4604', '-0.1655', '-0.2246', '0.4072', '-0.013794', '0.09717', '0.3538', '-0.977', '-0.1532', '-0.4421', '0.1965', '-0.1638', '0.1362', '-0.589', '0.462', '-0.3582', '0.1559', '0.2883', '0.02869', '-0.3394', '-0.2178', '-0.3867', '0.435', '-0.511', '-0.3523', '-0.076', '0.3801', '0.72', '0.7534', '-0.356', '0.252', '0.128', '0.1127', '-0.03464', '-0.1572', '-0.1874', '-0.2413', '-0.251', '0.457', '0.5166', '-0.2007', '0.591', '-0.2103', '0.1837', '0.02785']",C84609,,D055036,733.29,,,
mondo:0007252,Gordon syndrome,"['Gordon syndrome', 'distal arthrogryposis type 3', 'arthrogryposis distal type 3', 'arthrogryposis multiplex congenita, distal, type 2A', 'arthrogryposis, distal, type 3', 'camptodactyly, cleft palate, and clubfoot', 'distal arthrogryposis type IIA', 'DA3', 'camptodactyly-cleft palate-clubfoot syndrome']",0111607,114300,376,C0220666,"['0.04056', '-0.02596', '0.1956', '-0.1844', '0.317', '-0.4124', '0.05685', '0.2742', '-0.381', '-0.6587', '0.2512', '0.098', '-0.05673', '0.11664', '-0.01625', '0.2225', '0.2778', '-0.2532', '0.198', '-0.5747', '0.1343', '0.1708', '0.355', '0.156', '0.2488', '0.1963', '-0.1676', '-0.005592', '0.5205', '-0.04333', '0.1508', '-0.4045', '0.1375', '0.636', '0.02332', '-0.4172', '-0.0401', '-0.071', '-0.0761', '0.059', '-0.2274', '-0.3584', '-0.0826', '0.11346', '0.1401', '-0.417', '-0.00796', '0.597', '-0.0837', '-0.1512', '-0.3567', '-0.0713', '-0.332', '-0.3464', '-0.1638', '-0.5146', '-0.04788', '-0.652', '-0.1483', '-0.05157', '0.2461', '-0.1693', '-0.2664', '0.18', '-0.3298', '-0.0817', '0.1074', '0.3818', '-0.291', '0.2905', '-0.5522', '0.1617', '0.2192', '-0.2268', '0.2361', '0.1963', '-0.0781', '-0.1869', '-0.5156', '-0.2776', '0.2659', '0.2976', '0.3914', '0.6406', '-0.09265', '0.2318', '-0.092', '0.4026', '-0.02696', '0.1455', '0.1403', '0.372', '0.2197', '-0.04752', '0.628', '0.117', '0.3865', '-0.352', '0.1707', '-0.04126']",,,C537288,579.8,,,
mondo:0007253,"cancer, familial, with in vitro Radioresistance","['cancer, familial, with in vitro RADIORESISTANCE']",,114450,,C1861915,,,,C566179,,,,
mondo:0007254,breast cancer,"['mammary neoplasm', 'breast tumour', 'malignant tumour of the breast', 'mammary cancer', 'malignant tumour of breast', 'breast tumor', 'mammary tumor', 'malignant tumor of the breast', 'malignant breast neoplasm', 'mammary tumour', 'primary breast cancer', 'breast cancer', 'malignant breast tumour', 'malignant neoplasm of the breast', 'malignant tumor of breast', 'malignant neoplasm of breast', 'cancer of breast', 'malignant breast tumor']",1612,,,,,C9335,,,174.8,C50,,
mondo:0007256,hepatocellular carcinoma,"['hepatoblastoma, somatic', 'liver cancer', 'liver carcinoma', 'cancer, hepatocellular', 'liver cell cancer (hepatocellular carcinoma)', 'adult primary hepatocellular carcinoma', 'hepatocellular cancer, somatic', 'hepatoblastoma caused by somatic mutation', 'adult hepatoma', 'carcinoma of liver cells', 'hepatocellular carcinoma, childhood type, somatic', 'primary carcinoma of liver cells', 'carcinoma of the liver cells', 'hepatoma', 'hepatoblastoma', 'liver and intrahepatic bile duct carcinoma', 'hepatocellular carcinoma, somatic', 'carcinoma, hepatocellular, malignant', 'hepatocellular cancer', 'HCC', 'primary carcinoma of the liver cells', 'carcinoma of liver', 'liver cell carcinoma', 'hepatocellular carcinoma', 'hepatocellular adenocarcinoma']",686,114550,88673,,"['0.1816', '0.07874', '-0.4648', '0.3687', '-0.01297', '-0.0798', '0.1416', '0.5264', '0.256', '0.05212', '0.001277', '0.0698', '-0.3945', '0.2893', '-0.519', '-0.3352', '-0.2238', '-0.265', '0.06696', '-0.4004', '-0.303', '-0.3835', '0.7666', '-0.402', '0.2634', '-0.1799', '0.06647', '-0.00823', '-0.1315', '-0.5557', '0.69', '-0.5225', '0.3342', '-0.3955', '0.1581', '-0.2625', '-0.7695', '-0.3042', '-0.01498', '0.139', '-0.234', '-0.05914', '0.11755', '-0.2737', '-0.03754', '0.2637', '-0.24', '-0.338', '-0.05774', '-0.2292', '0.4233', '0.404', '-0.1542', '0.2212', '-0.4807', '0.184', '0.4438', '-0.3684', '-0.5425', '0.02643', '0.3708', '0.4072', '-0.03897', '-0.09015', '-0.1965', '0.1766', '0.1952', '0.4434', '0.066', '0.3765', '0.1947', '0.2568', '0.311', '0.1475', '0.147', '-0.00567', '-0.255', '-0.16', '-0.01735', '-0.7095', '-0.8315', '-0.2085', '-0.4868', '-0.1332', '-0.2141', '-0.3784', '0.441', '-0.419', '0.4094', '-0.3613', '0.4175', '0.1775', '-0.3826', '-0.2322', '0.6875', '0.1946', '0.09814', '-0.67', '-0.1267', '-0.311']",C3099,0000182,D006528,,,10049010,
mondo:0007257,"candidiasis, familial, 1","['Cmct', 'candidiasis, familial, 1', 'candidiasis, familial chronic mucocutaneous, autosomal dominant, with or without thyroid disease', 'candidiasis, familial, 1, autosomal dominant', 'CANDF1']",,114580,,C2751429,,,,C567779,,,,
mondo:0007258,"canine teeth, absence of upper permanent","['canine teeth, absence of upper permanent']",,114600,,C1861899,,,,,,,,
mondo:0007259,craniofaciofrontodigital syndrome,"['Cantu craniofaciofrontodigital syndrome', 'craniofaciofrontodigital syndrome']",,114620,363705,C2676032,,,,C567298,,,,
mondo:0007260,Car factor deficiency,['Car factor deficiency'],,114650,,C1861898,,,,C566176,,,,
mondo:0007261,Carabelli anomaly of maxillary molar teeth,['Carabelli anomaly of maxillary molar teeth'],,114700,,C1861897,,,,C566175,,,,
mondo:0007263,cardiac rhythm disease,['arrhythmia'],,,,,,C2881,0004269,,427.9,,,
mondo:0007265,cardiofaciocutaneous syndrome 1,"['BRAF cardiofaciocutaneous syndrome', 'CFC syndrome', 'cardiofaciocutaneous syndrome caused by mutation in BRAF', 'CFC1', 'cardiofaciocutaneous syndrome', 'cardiofaciocutaneous syndrome type 1', 'cardiofaciocutaneous syndrome 1', 'Cfcs']",0111460,115150,,CN029449,,,,,,,,
mondo:0007266,hypertrophic cardiomyopathy 2,"['hypertrophic cardiomyopathy caused by mutation in TNNT2', 'CMH2', 'cardiomyopathy, hypertrophic, 2', 'cardiomyopathy, familial hypertrophic, 2', 'TNNT2 hypertrophic cardiomyopathy', 'hypertrophic cardiomyopathy type 2', 'cardiomyopathy, familial hypertrophic, type 2', 'familial hypertrophic cardiomyopathy type 2', 'cardiomyopathy familial hypertrophic 2']",0110308,115195,,C1861864,,C142892,,C566171,,,,
mondo:0007267,hypertrophic cardiomyopathy 3,"['CMH3', 'TPM1 hypertrophic cardiomyopathy', 'cardiomyopathy, hypertrophic, 3', 'hypertrophic cardiomyopathy caused by mutation in TPM1', 'cardiomyopathy, familial hypertrophic, type 3', 'cardiomyopathy, familial hypertrophic, 3', 'hypertrophic cardiomyopathy type 3', 'cardiomyopathy familial hypertrophic 3']",0110309,115196,,C1861863,,,,C566170,,,,
mondo:0007268,hypertrophic cardiomyopathy 4,"['hypertrophic cardiomyopathy caused by mutation in MYBPC3', 'cardiomyopathy, familial hypertrophic, type 4', 'cardiomyopathy, familial hypertrophic, 4, susceptibility to', 'cardiomyopathy, familial hypertrophic, 4', 'MYBPC3 hypertrophic cardiomyopathy', 'CMH4', 'familial hypertrophic cardiomyopathy type 4', 'cardiomyopathy, hypertrophic, 4', 'hypertrophic cardiomyopathy type 4']",0110310,115197,,C1861862,,C133725,,C566169,,,,
mondo:0007269,dilated cardiomyopathy 1A,"['cardiomyopathy, dilated, 1A', 'cardiomyopathy, congestive', 'dilated cardiomyopathy type 1A', 'cardiomyopathy, familial idiopathic', 'CDCD1', 'dilated cardiomyopathy with conduction defect 1', 'cardiomyopathy, idiopathic dilated', 'familial isolated dilated cardiomyopathy caused by mutation in LMNA', 'LMNA familial isolated dilated cardiomyopathy', 'familial dilated cardiomyopathy with conduction defect due to LMNA mutation', 'cardiomyopathy, dilated, with conduction defect 1', 'cardiomyopathy dilated with conduction defect type 1', 'cardiomyopathy, dilated, type 1A']",0110425,115200,300751,C1449563,"['-0.5415', '-0.513', '-0.1548', '0.3748', '0.5737', '-0.329', '0.6133', '0.5776', '0.3032', '-0.3772', '0.924', '-0.08435', '-0.815', '0.257', '-0.891', '-0.5913', '-0.786', '-0.0993', '-0.4375', '-1.137', '0.391', '0.539', '-0.01674', '0.102', '-0.4111', '-0.588', '-0.526', '0.5327', '-0.3198', '-0.2888', '1.267', '0.3992', '0.817', '0.1576', '0.02142', '-0.575', '-0.11707', '-0.1328', '0.7847', '-0.5767', '0.2139', '0.5845', '0.8115', '0.507', '0.2712', '0.3755', '-0.5103', '0.5845', '0.1581', '0.1917', '-0.3013', '-0.1799', '0.361', '-0.3005', '0.2756', '-0.652', '-0.3855', '-0.2778', '-0.504', '0.0641', '0.3687', '0.5356', '0.073', '-0.758', '-1.009', '0.77', '0.0942', '1.171', '-0.6357', '-0.4802', '-0.494', '0.1897', '0.5054', '-0.1489', '0.164', '0.415', '0.6714', '-0.086', '0.06445', '0.1971', '0.4775', '-0.4622', '0.4534', '-0.559', '0.9097', '0.2034', '0.4583', '-0.09564', '0.4744', '0.2059', '0.3223', '0.05057', '-0.604', '0.2883', '0.6606', '0.6245', '0.6504', '0.01869', '-0.5615', '0.01493']",,,,,,,
mondo:0007270,"cardiomyopathy, familial restrictive, 1","['Rcm', 'RCM1', 'TNNI3 familial isolated restrictive cardiomyopathy', 'familial isolated restrictive cardiomyopathy caused by mutation in TNNI3', 'cardiomyopathy, familial restrictive, 1', 'cardiomyopathy, familial restrictive, type 1']",0111425,115210,,C1861861,,,,C566168,,,,
mondo:0007271,familial cutaneous collagenoma,"['collagenoma, familial cutaneous']",,115250,53296,C0406817,,,,C562925,,,,
mondo:0007272,hereditary hypercarotenemia and vitamin A deficiency,"['Carotenoids, plasma level of, quantitative trait locus 1', 'HCVAD', 'hypercarotenemia and vitamin A deficiency, autosomal dominant']",,115300,199285,,"['-0.225', '-0.08203', '-0.2817', '-0.002201', '0.45', '-0.1761', '-0.631', '0.3875', '-0.159', '-0.003603', '0.143', '0.1511', '0.1323', '-0.1406', '-0.00971', '0.1309', '0.4087', '0.3235', '-0.245', '-0.555', '0.04895', '-0.4287', '0.3694', '0.04254', '0.2734', '-0.0241', '-0.0271', '-0.2625', '-0.101', '-0.348', '0.1243', '0.11597', '-0.087', '0.1335', '-0.272', '-0.2203', '-0.1719', '-0.4385', '0.1996', '-0.2074', '-0.01639', '-0.6685', '0.10394', '-0.568', '-0.0777', '-0.481', '0.0762', '0.1907', '0.03061', '-0.1361', '-0.06586', '-0.2104', '0.1335', '0.2168', '-0.565', '0.08264', '0.4338', '-0.4443', '-0.4202', '0.117', '0.2517', '0.2534', '0.527', '-0.3743', '0.1248', '-0.1159', '0.2222', '0.692', '-0.6953', '-0.05508', '-0.04608', '-0.3728', '-0.09674', '-0.08746', '0.2', '0.4375', '0.147', '0.09735', '0.1323', '-0.03473', '0.3704', '-0.1578', '0.0316', '-0.02373', '0.06525', '0.1197', '0.10223', '0.3718', '0.608', '0.1627', '0.5557', '0.3767', '-0.2166', '-0.176', '0.6455', '0.569', '0.1766', '-0.4087', '-0.1844', '0.0203']",,,C567296,,,,
mondo:0007273,paragangliomas 4,"['paragangliomas 4', 'paraganglioma caused by mutation in SDHB', 'paragangliomas, hereditary extraadrenal', 'SDHB paraganglioma', 'pheochromocytoma, familial extraadrenal', 'paraganglioma, familial malignant', 'carotid body tumours and multiple extraadrenal Pheochromocytomas', 'SDHB-related hereditary paraganglioma-pheochromocytoma syndrome', 'carotid body tumors and multiple extraadrenal Pheochromocytomas', 'pheochromocytoma, extraadrenal, and cervical paraganglioma', 'PGL4', 'paragangliomas type 4', 'pheochromocytoma, extraadrenal and cervical paraganglioma']",,115310,,C1861848,,,,,,,,
mondo:0007274,carpal displacement,"['carpal bossing', 'carpal displacement']",,115400,,C1861847,,,,,,,,
mondo:0007275,carpal tunnel syndrome,"['CTS', 'carpal tunnel median neuropathy', 'median nerve entrapment', 'amyotrophy, thenar, of carpal origin', 'carpal tunnel syndrome', 'CTS - carpal tunnel syndrome']",12169,,50838,C0007286,"['-0.003597', '-0.2369', '-0.06195', '0.712', '0.0258', '0.0882', '0.4075', '0.511', '-0.711', '-0.728', '0.1359', '0.5225', '-0.0003674', '0.583', '0.1124', '-0.2898', '-0.069', '0.1126', '-0.3438', '-0.8833', '0.186', '0.2355', '-0.2146', '0.2786', '0.3254', '0.01103', '0.05344', '0.11755', '0.4858', '0.1865', '-0.2957', '0.0972', '0.07837', '0.11316', '0.2418', '-0.09576', '0.2358', '-0.5464', '0.985', '-0.6396', '-0.1646', '-0.0118', '-0.4014', '-0.1191', '1.138', '-0.1256', '-0.173', '0.3596', '0.6475', '0.681', '-0.5938', '-0.06097', '0.31', '0.7744', '-0.5513', '0.1589', '-0.3145', '-0.454', '-0.7583', '-0.7207', '-0.1068', '0.03735', '-0.002302', '-0.1614', '-0.519', '0.108', '-0.02948', '0.9805', '-0.2201', '0.6406', '0.01953', '-0.01817', '0.5083', '-0.722', '0.4912', '0.792', '0.05826', '0.938', '-0.555', '-0.2194', '-0.167', '0.1403', '-0.0541', '0.2211', '0.3047', '0.1256', '-0.664', '0.545', '0.333', '0.2399', '-0.1658', '-0.1115', '-0.273', '0.4326', '0.248', '-0.743', '-0.1042', '-0.7764', '-0.134', '-0.04742']",C34450,0004143,D002349,354.0,G56.0,,
mondo:0007276,cat-eye syndrome,"['cat-eye syndrome (Type I)', 'CES', 'Inv dup(22)(q11)', 'CAT eye syndrome', 'chromosome 22 partial tetrasomy', 'Schmid-Fraccaro syndrome']",,115470,195,C0265493,,C75477,,C535918,,,,
mondo:0007277,cataract-aberrant oral frenula-growth delay syndrome,"['cataracts, aberrant oral frenula, and growth retardation', 'Wellesley-Carman-French syndrome', 'Wellesley Carmen French syndrome', 'cataract, aberrant oral frenula, and growth retardation']",,115645,1373,,,,,C536691,,,,
mondo:0007278,cataract 32 multiple types,"['cataract 32, multiple types', 'CTAA1', 'CTPP5', 'CTRCT32', 'posterior polar cataract 5', 'anterior polar cataract 1', 'cataract, anterior polar, 1', 'cataract, anterior polar', 'cataract, posterior polar, 5']",0110227,115650,98993,C1855179,"['-0.3215', '0.0842', '0.02264', '0.171', '-0.01646', '-0.1611', '-0.00502', '0.4155', '-0.2642', '-0.2482', '-0.05292', '-0.2072', '-0.116', '0.2595', '-0.2', '-0.2087', '0.0395', '-0.1771', '0.0762', '-0.4954', '0.05557', '-0.0781', '0.04175', '-0.11633', '0.04654', '-0.0008636', '-0.0878', '0.05988', '-0.0904', '0.1702', '0.136', '-0.1874', '0.1471', '0.232', '0.0206', '0.0676', '0.1674', '-0.1219', '-0.10516', '-0.2325', '0.289', '-0.1512', '-0.0002549', '0.1471', '-0.09534', '-0.1948', '0.07104', '-0.1028', '0.1587', '0.08374', '0.1493', '0.01326', '0.0839', '0.07544', '-0.04633', '-0.24', '0.4648', '-0.0733', '-0.2705', '-0.01717', '0.2283', '-0.10815', '0.05173', '0.1819', '-0.1958', '0.1451', '0.4106', '0.3757', '0.008446', '0.1366', '-0.2578', '0.2318', '0.2032', '0.0385', '0.004562', '0.11615', '0.109', '0.01438', '-0.2764', '-0.0637', '-0.1215', '0.1396', '-0.10614', '0.222', '0.06058', '-0.2115', '0.1547', '0.1', '0.22', '0.153', '0.2146', '0.288', '0.07477', '-0.0001539', '0.3025', '-0.1426', '0.2903', '-0.2197', '0.0909', '0.05392']",,,,,,,
mondo:0007279,cataract 7,"['CTRCT7', 'cataract 7, cerulean type', 'cerulean type cataract 7', 'cataract 7', 'CCA1', 'congenital cerulean type cataract 1', 'cataract, congenital, cerulean type, 1', 'cataract type 7']",0110260,115660,,,,,,,,,,
mondo:0007280,cataract 8 multiple types,"['cataract congenital Volkmann type', 'CTRCT8', 'cataract, congenital, Volkmann type', 'cataract 8, multiple types']",0110228,115665,98983,C1861833,,,,C538285,,,,
mondo:0007281,cataract 4 multiple types,"['cataract, congenital, cerulean type, 3', 'cataract 4, multiple types', 'CTRCT4', 'cataract 4 multiple types with or without microcornea', 'cataract, Nonnuclear polymorphic congenital', 'cataract, crystalline aculeiform', 'congenital cataract cerulean type 3', 'CRYGD cataract (disease)', 'cataract 4, multiple types, with or without microcornea', 'cataract, punctate, progressive juvenile-onset', 'CCA3']",0110234,115700,98995,,"['-0.08813', '0.1233', '0.00463', '0.05487', '0.06683', '-0.1558', '-0.0763', '0.2446', '-0.1838', '-0.0942', '-0.05215', '-0.0351', '-0.02089', '0.06616', '-0.0675', '-0.03043', '-0.00364', '-0.11676', '-0.00915', '-0.3284', '-0.01962', '-0.03378', '0.08777', '-0.02931', '0.0699', '-0.0481', '-0.04413', '0.0457', '-0.02477', '0.0269', '0.1285', '-0.04626', '0.1097', '0.163', '0.00838', '-0.02686', '0.03973', '-0.0373', '0.004684', '-0.058', '0.05652', '-0.05307', '0.0702', '0.01907', '-0.04315', '-0.06036', '-0.02164', '0.1558', '0.04062', '0.0347', '0.002445', '-0.1251', '0.04037', '-0.03372', '-0.006714', '-0.0503', '0.2426', '-0.03818', '-0.1262', '-0.04755', '0.1145', '-0.00558', '0.01249', '0.06033', '-0.01249', '0.04666', '0.2474', '0.2235', '-0.06604', '0.1455', '-0.08435', '0.1077', '0.06223', '-0.1307', '0.06256', '-0.003056', '0.01717', '-0.04398', '-0.1449', '-0.0787', '-0.05225', '0.0157', '-0.05032', '0.1149', '-0.03766', '-0.006207', '0.03357', '0.0903', '0.1445', '0.0633', '0.08484', '0.1346', '0.05002', '0.04898', '0.2593', '-0.00435', '0.1313', '-0.10986', '0.002573', '0.01956']",,,,,,,
mondo:0007282,cataract 29,"['cataract 29', 'cataract 29 coralliform', 'cataract type 29', 'cataract 29, coralliform', 'CTRCT29']",0110232,115800,,C3805409,,,,,,,,
mondo:0007283,cataract 42,"['cataract 42', 'early-onset non-syndromic cataract caused by mutation in CRYBA2', 'CRYBA2 early-onset non-syndromic cataract', 'cataract type 42', 'CTRCT42', 'A cataract that has_material_basis_in heterozygous mutation in the CRYBA2 gene on chromosome 2q35.']",0110237,115900,,C4011454,,,,,,,,
mondo:0007284,cataract 20 multiple types,"['CRYGS cataract (disease)', 'CTRCT20', 'cataract 20, multiple types']",0110240,116100,98994,,,,,,,,,
mondo:0007285,cataract 1 multiple types,"['cataract 1, multiple types', 'CAE1', 'GJA8 cataract (disease)', 'CZP1', 'zonular pulverulent cataract 1', 'CTRCT1', 'cataract, Duffy-linked', 'cataract 1, multiple types, with or without microcornea', 'cataract, zonular pulverulent, 1', 'Duffy linked cataract']",0110231,116200,98984,C1861828,"['-0.3435', '0.1282', '0.00367', '0.2708', '0.02148', '-0.2207', '-0.05557', '0.4067', '-0.3748', '-0.2578', '0.0109', '-0.2617', '-0.185', '0.2343', '-0.0909', '-0.2737', '0.0698', '-0.05475', '0.0541', '-0.4758', '0.1292', '-0.01073', '-0.001765', '-0.09247', '0.06995', '0.02734', '-0.0224', '0.1233', '-0.02312', '0.2024', '0.1257', '-0.1693', '0.1725', '0.2585', '0.0757', '0.06946', '0.1603', '-0.184', '-0.03412', '-0.2522', '0.3176', '-0.1646', '0.00954', '0.1722', '-0.12366', '-0.2751', '0.0964', '-0.1562', '0.2605', '0.029', '0.2125', '0.01984', '0.1372', '0.0434', '-0.02559', '-0.2998', '0.552', '0.03183', '-0.3062', '-0.03424', '0.2035', '-0.0843', '0.1786', '0.0875', '-0.1766', '0.266', '0.3606', '0.3123', '0.02402', '0.157', '-0.371', '0.118', '0.2583', '0.0138', '0.06287', '0.04422', '0.10077', '0.1181', '-0.3218', '0.0356', '-0.1821', '0.0792', '-0.1189', '0.1583', '0.1454', '-0.3606', '0.2659', '0.2476', '0.1893', '0.3018', '0.2223', '0.1862', '0.0335', '-0.07416', '0.296', '-0.11346', '0.3562', '-0.297', '0.126', '-0.03114']",,,C566158,,,,
mondo:0007286,cataract 30,"['cataract type 30', 'cataract Coppock-like', 'cataract 30 pulverulent', 'cataract 30, pulverulent', 'cataract 30, multiple types', 'cataract 30', 'CTRCT30']",0110248,116300,,C3805411,,,,C566157,,,,
mondo:0007287,cataract 41,"['cataract 41', 'cataract type 41', 'cataract 41, congenital nuclear type', 'congenital nuclear type cataract 41', 'CTRCT41', 'early-onset non-syndromic cataract caused by mutation in WFS1', 'WFS1 early-onset non-syndromic cataract']",0110241,116400,,C3805412,,,,,,,,
mondo:0007288,cataract 6 multiple types,"['Posterior polar cataract, 1', 'CTPA', 'CTPP1', 'age related cortical cataract 2', 'ARCC2', 'cataract, age-related cortical, 2', 'CTRCT6', 'posterior polar cataract 1', 'cataract 6, multiple types', 'cataract, posterior polar, 1', 'CTPP', 'EPHA2 cataract (disease)']",0110229,116600,98994,,"['-0.3127', '0.1489', '0.0833', '0.1114', '0.0964', '-0.06052', '-0.02327', '0.1775', '-0.3215', '-0.10785', '-0.1512', '-0.12213', '-0.05038', '0.02882', '-0.1658', '-0.0968', '0.08093', '-0.1471', '0.11633', '-0.3389', '-0.0919', '0.01987', '0.10345', '-0.02266', '0.03186', '0.0775', '-0.09174', '0.1013', '-0.007473', '0.09735', '0.10754', '-0.08936', '0.12384', '0.1558', '0.09955', '0.02776', '0.1686', '-0.1335', '-0.010475', '-0.2822', '0.1334', '-0.154', '0.10657', '0.03864', '-0.05884', '0.03122', '0.01292', '0.1924', '0.1075', '0.03845', '0.10223', '-0.0952', '0.10724', '-0.05618', '-0.03995', '-0.1489', '0.3418', '-0.05933', '-0.2338', '-0.0224', '0.1389', '-0.0856', '0.02913', '0.0957', '-0.0882', '0.0493', '0.3247', '0.2795', '-0.05728', '0.1517', '-0.1978', '0.03757', '0.1162', '-0.181', '0.05988', '0.06223', '-0.0243', '-0.1151', '-0.0966', '-0.0646', '-0.0786', '0.1404', '-0.0683', '0.235', '-0.1095', '0.00432', '0.000639', '0.1375', '0.1091', '0.007355', '0.04797', '0.1265', '0.1237', '0.1125', '0.3542', '-0.1602', '0.1704', '-0.2822', '-0.0599', '0.1501']",,,,,,,
mondo:0007289,cataract 13 with adult I phenotype,"['CTRCT13', 'cataract 13 with adult I phenotype', 'cataract 13 with ADULT I phenotype']",0110242,116700,,C3805373,"['-0.002747', '0.00888', '-0.000659', '0.000501', '0.002289', '-0.0251', '0.007317', '0.03925', '-0.02826', '-0.006477', '-0.00913', '-0.01236', '0.00696', '0.012344', '-0.007553', '-0.0192', '0.00508', '-0.01756', '-0.01327', '-0.03336', '-0.00945', '-0.01697', '0.015015', '-0.0007024', '0.00986', '-0.001359', '-0.004307', '-0.003403', '0.003887', '-0.01872', '0.02145', '0.001777', '0.03296', '0.009995', '0.01306', '-0.01733', '-0.00971', '-0.004204', '-0.013504', '-0.02786', '0.011856', '-0.01312', '0.01249', '-0.005093', '0.003061', '-0.02277', '0.000995', '0.0262', '0.00888', '0.01794', '-0.00833', '0.004906', '-0.0003726', '0.00461', '-0.018', '-0.005245', '0.01692', '-0.00583', '-0.02151', '0.0016165', '0.0148', '0.01269', '0.003918', '-0.0008097', '0.003035', '0.001036', '0.02751', '0.01828', '-0.02295', '0.01465', '-0.00968', '0.003607', '0.0158', '-0.0106', '0.009445', '0.02173', '-0.00985', '-0.00893', '-0.001245', '-0.002115', '-0.00575', '-0.00578', '0.001301', '0.02106', '-0.00387', '-0.002148', '0.00569', '0.01846', '0.02626', '0.0035', '0.005207', '0.02585', '-0.010925', '0.01055', '0.0561', '0.00729', '0.02223', '-0.0211', '0.00757', '0.004322']",,,,,,,
mondo:0007290,cataract 5 multiple types,"['HSF4 cataract (disease)', 'cataract 5, multiple types', 'CTRCT5', 'cataract, Marner type', 'cataract, lamellar']",0110255,116800,98995,,"['-0.2678', '0.1049', '0.006123', '0.1881', '0.0308', '-0.1255', '0.01359', '0.41', '-0.2322', '-0.2216', '-0.06134', '-0.2047', '-0.1333', '0.2426', '-0.1823', '-0.1741', '0.04605', '-0.1768', '0.0924', '-0.4465', '0.05823', '-0.03268', '0.0413', '-0.1032', '0.03842', '-0.051', '-0.06433', '0.07465', '-0.0603', '0.1959', '0.1439', '-0.2174', '0.1389', '0.2527', '0.0377', '0.08984', '0.183', '-0.1248', '-0.10016', '-0.2379', '0.3127', '-0.1456', '-0.0539', '0.1302', '-0.1213', '-0.1887', '0.0734', '-0.0911', '0.1532', '0.0964', '0.162', '0.02179', '0.12213', '0.1077', '-0.03888', '-0.2227', '0.4229', '-0.08026', '-0.2732', '-0.03055', '0.2181', '-0.1077', '0.02573', '0.12286', '-0.2115', '0.1254', '0.4014', '0.3699', '0.02557', '0.1476', '-0.2502', '0.1951', '0.1791', '0.02687', '0.01804', '0.1185', '0.12463', '0.01498', '-0.274', '-0.07135', '-0.1256', '0.1084', '-0.0948', '0.1947', '0.08105', '-0.1907', '0.1475', '0.12463', '0.1854', '0.149', '0.1793', '0.255', '0.06665', '0.0372', '0.251', '-0.1384', '0.2563', '-0.2456', '0.10516', '0.06506']",,,C535342,,,,
mondo:0007293,leukocyte adhesion deficiency 1,"['leukocyte adhesion deficiency caused by mutation in ITGB2', 'Lad1', 'lymphocyte function-associated antigen 1 immunodeficiency', 'LFA 1 immunodeficiency', 'lad 1', 'leukocyte adhesion deficiency, type I', 'lad', 'LFA-I deficiency', 'lad-I', 'leukocyte adhesion deficiency', 'LFA1 immunodeficiency', 'leukocyte adhesion deficiency type 1', 'Lfa1 immunodeficiency', 'ITGB2 leukocyte adhesion deficiency', 'lad-type I', 'leukocyte adhesion deficiency type I', 'leukocyte adhesion deficiency, type 1', 'LAD1']",0110910,116920,99842,C0398738,"['0.2245', '0.0869', '-0.331', '-0.2979', '0.2505', '-0.2428', '0.02379', '0.36', '-0.2385', '0.2517', '-0.4424', '-0.01554', '-0.1282', '0.2808', '-0.10474', '-0.1439', '-0.0678', '-0.3557', '0.2837', '-0.991', '-0.8345', '-0.3042', '0.6675', '0.3057', '0.3643', '0.0745', '-0.1704', '0.8457', '-0.668', '-0.153', '0.1437', '0.7407', '-0.1534', '-0.0921', '-0.3696', '0.396', '-0.2812', '-0.0327', '0.02618', '-0.273', '-0.03726', '-0.02745', '0.01258', '0.0812', '-0.428', '0.1345', '-0.2727', '-0.7373', '0.2439', '0.3994', '-0.099', '-0.3708', '0.2203', '-0.0331', '-0.06665', '-0.03168', '0.11804', '0.5596', '0.2125', '-0.11224', '-0.321', '0.6763', '-0.2032', '0.0647', '0.635', '0.0979', '0.52', '-0.1582', '-0.4048', '0.797', '-0.4587', '-0.3381', '-0.3635', '-0.3218', '0.6562', '0.1896', '0.164', '0.401', '0.02046', '0.258', '-0.4272', '-0.4636', '-0.1902', '-0.02353', '-0.2761', '-0.1022', '0.1206', '0.6177', '0.4922', '-0.2184', '-0.112', '0.7065', '-0.007244', '-0.558', '0.725', '0.5957', '-0.1359', '-0.6357', '0.6416', '0.402']",C4689,,C535887,,,,
mondo:0007294,central core myopathy,"['myopathy, central fibrillar', 'central CORE disease of muscle', 'multicore myopathy, moderate, with hand involvement', 'muscular central core disease', 'muscle core disease', 'myopathy, central core', 'neuromuscular disease, congenital, with uniform type 1 Fiber', 'CCD', 'multiminicore disease, moderate, with hand involvement', 'neuromuscular disease, congenital, with uniform type 1 Fibre', 'Shy-Magee syndrome', 'central core disease', 'minicore myopathy, moderate, with hand involvement', 'Cco']",3529,117000,598,C1861753,"['-0.0743', '0.03705', '0.04874', '-0.02914', '-0.02077', '-0.1506', '0.001519', '0.1428', '-0.1289', '-0.0429', '-0.05475', '0.01449', '0.009926', '0.0342', '6.09e-05', '-0.08154', '-0.02574', '-0.08966', '-0.07404', '-0.2494', '0.003807', '-0.01437', '0.10205', '0.02095', '0.04453', '-0.0364', '0.006104', '-0.00729', '-0.02708', '-0.0671', '0.006676', '-0.006527', '0.12366', '0.0781', '0.0758', '-0.09393', '-0.05554', '-0.065', '-0.000558', '-0.1614', '0.013695', '-0.1608', '-0.005783', '0.0215', '0.043', '-0.07446', '-0.08575', '0.0906', '-0.0366', '0.02599', '-0.06744', '-0.00791', '0.02502', '-0.01997', '-0.081', '-0.0786', '0.0982', '-0.0557', '-0.10474', '-0.0271', '0.09045', '-0.002584', '-0.0289', '0.01349', '-0.03625', '0.001398', '0.1062', '0.09656', '-0.07623', '0.1126', '-0.124', '0.0074', '0.0283', '-0.07764', '0.08746', '0.0668', '0.010025', '-0.05426', '-0.04306', '-0.05206', '-0.01958', '0.0033', '0.03986', '0.1254', '-0.00082', '0.0636', '-0.03558', '0.112', '0.175', '-0.010445', '0.07007', '0.1272', '0.01418', '0.03152', '0.2769', '0.0708', '0.08887', '-0.1921', '0.02298', '0.02707']",C83010,1000855,D020512,,,,
mondo:0007295,childhood epilepsy with centrotemporal spikes,"['centrotemporal epilepsy', 'benign familial epilepsy of childhood with rolandic spikes', 'BCECTS', 'BRE', 'benign Rolandic epilepsy of childhood (BREC)', 'sylvan seizures', 'centrotemporal epilepsy, isolated cases', 'centralopathic epilepsy', 'benign childhood epilepsy with centrotemporal spike', 'benign Rolandic epilepsy', 'BECRS', 'benign epilepsy with centro-temporal spikes (BECTS)', 'Rolandic epilepsy', 'benign childhood epilepsy with centrotemporal spikes', 'benign epilepsy of childhood with centrotemporal spikes', 'BECTS', 'benign epilepsy of childhood with centrotemporal spikes (BECCT)', 'temporal-central focal epilepsy', 'benign epilepsy with centrotemporal spikes', 'benign Rolandic epilepsy (BRE)']",3329,117100,1945,CN200685,"['1.111', '0.2988', '-0.3489', '-0.152', '-0.5215', '-0.1133', '0.8433', '0.556', '-0.67', '-0.493', '-0.11615', '-0.2686', '-0.1897', '0.3445', '0.0535', '0.11847', '-0.582', '-0.7754', '-0.2708', '-0.3813', '-0.1666', '0.425', '-0.00843', '-0.5625', '-0.07794', '-0.05246', '-0.2686', '-0.1497', '-0.5923', '0.342', '0.1896', '-0.745', '0.3762', '0.08563', '0.6167', '0.3425', '-0.04706', '0.1451', '-0.0934', '-0.2742', '0.02576', '-0.2396', '0.05948', '-0.401', '-0.284', '-0.4011', '-0.4104', '0.1733', '0.4023', '0.848', '0.06396', '0.137', '-0.0805', '-0.3083', '0.178', '-0.2274', '-0.2827', '0.06134', '-0.0696', '0.4653', '-0.807', '0.462', '0.65', '-0.373', '-0.2152', '1.203', '-0.02965', '0.11957', '-0.5303', '0.644', '0.7334', '0.8325', '-0.1037', '-0.3567', '0.5044', '0.6445', '0.786', '0.3923', '-0.5146', '0.1877', '-0.03235', '0.409', '0.3906', '0.1451', '0.3', '0.2347', '0.3418', '0.7793', '0.4553', '0.4565', '-0.002674', '0.1663', '-0.292', '-0.004425', '0.0998', '0.067', '0.375', '-0.7114', '0.3984', '0.234']",C116538,,,345.80,,,
mondo:0007296,spinocerebellar ataxia type 31,"['SCA31', 'spinocerebellar ataxia, 16Q22-linked', 'spinocerebellar ataxia type 31', 'spinocerebellar ataxia 16q22-linked', 'spinocerebellar ataxia 31']",0050980,117210,217012,C4274986,"['-0.08374', '-0.0797', '-0.1565', '0.02966', '-0.0853', '-0.7144', '0.2612', '0.4102', '-0.4783', '-0.863', '0.355', '0.111', '-0.0709', '0.08264', '0.748', '-0.3223', '-0.2025', '-0.636', '0.03513', '-0.92', '-0.3044', '-0.4128', '0.1108', '-0.4873', '0.3147', '-0.4727', '-0.4077', '0.2332', '0.0845', '-0.629', '0.1875', '0.319', '-0.3474', '-0.1748', '0.1997', '0.05353', '0.00946', '0.10986', '0.3125', '0.471', '0.438', '0.3518', '-0.263', '0.44', '0.509', '-0.4673', '-0.1026', '0.452', '0.3064', '-0.113', '-0.10254', '0.004738', '-0.0759', '-0.6475', '0.1315', '-0.621', '0.6133', '0.2299', '-0.03668', '0.3618', '-0.4697', '0.3474', '0.2406', '-0.2223', '-0.359', '0.3523', '0.2979', '0.639', '-0.3953', '0.568', '0.867', '0.2935', '-0.1782', '-0.7065', '0.925', '0.2152', '0.3643', '-0.099', '0.09204', '0.3496', '-0.1294', '-0.93', '0.645', '0.7905', '-0.2717', '-0.491', '0.07697', '0.0805', '0.503', '0.5444', '0.1918', '0.279', '-0.0834', '-0.0974', '0.988', '0.852', '0.3994', '0.5083', '-0.3225', '-0.1907']",C176901,,C566146,,,,
mondo:0007297,ADan amyloidosis,"['cerebellar ataxia, cataract, deafness, and dementia or psychosis', 'familial Danish dementia', 'FDD', 'dementia, familial Danish', 'HOOE', 'familial dementia, Danish type', 'ITM2B-related cerebral amyloid angiopathy 2', 'cerebral amyloid angiopathy, ITM2B-RELATED, 2', 'cerebral amyloid angiopathy, ITM2B-related, type 2', 'Heredopathia Ophthalmootoencephalica', 'cerebellar ataxia, cataract, deafness, and dementia Or psychosis']",0070030,117300,97346,C1861735,"['0.2957', '-0.7627', '-0.4673', '0.2108', '0.2678', '-0.509', '-0.7915', '0.3708', '-1.417', '0.1768', '-0.2747', '-0.1837', '-1.03', '0.1265', '-0.341', '-0.2462', '0.2253', '-0.2177', '-0.1112', '-0.599', '0.4214', '-0.1342', '0.0519', '-0.04318', '0.03378', '0.6304', '-0.5977', '-0.278', '0.4692', '0.2333', '0.4133', '-0.3254', '0.8975', '-1.014', '0.4492', '-0.6963', '-0.596', '0.1832', '0.02777', '-0.123', '0.2223', '-0.1947', '-0.2551', '0.3777', '0.4602', '-0.5854', '-0.399', '0.325', '0.359', '0.459', '0.131', '1.019', '0.1528', '-0.4365', '-0.2979', '-0.2316', '0.5225', '-0.02393', '-0.644', '-0.7666', '-0.3838', '0.272', '0.603', '-0.702', '-0.363', '-0.366', '0.4246', '0.939', '-0.6255', '0.5996', '-0.3813', '0.4014', '-0.4238', '-0.4119', '0.1095', '0.6426', '-0.3538', '1.473', '-0.3333', '-0.8276', '-0.26', '-0.3418', '-0.1609', '0.0051', '0.4358', '-0.5605', '-0.1398', '-0.04858', '0.2252', '0.0829', '0.5073', '-0.431', '-0.3162', '-0.02596', '0.5283', '0.5234', '-0.645', '0.06097', '0.3286', '0.1338']",,,C538209,,,,
mondo:0007298,spinocerebellar ataxia type 29,"['spinocerebellar ataxia type 29', 'aplasia of cerebellar vermis', 'cerebellar ataxia, congenital nonprogressive, autosomal dominant', 'spinocerebellar ataxia 29', 'cerebellar ataxia early-onset nonprogressive', 'cerebellar vermis aplasia', 'spinocerebellar ataxia 29, congenital nonprogressive', 'ACV', 'SCA29', 'congenital nonprogressive spinocerebellar ataxia']",0050978,117360,208513,C4274987,"['-0.0731', '-0.283', '-0.003366', '-0.04172', '-0.1532', '-0.8643', '0.09845', '0.296', '-0.5923', '-0.916', '0.1812', '0.139', '-0.03467', '0.2576', '0.6304', '-0.2296', '-0.0683', '-0.3943', '0.04965', '-0.9385', '-0.1847', '-0.1904', '0.1254', '-0.5054', '0.3462', '-0.599', '-0.2542', '0.0348', '-0.223', '-0.693', '0.2261', '0.29', '-0.4756', '0.1178', '0.3137', '0.1119', '-0.1653', '0.1181', '0.367', '0.582', '0.4746', '0.1951', '-0.3792', '0.347', '0.579', '-0.4875', '0.1442', '0.296', '0.1965', '-0.001255', '-0.1482', '0.04477', '0.0864', '-0.4585', '0.132', '-0.5103', '0.4287', '0.42', '0.10236', '0.3555', '-0.4634', '0.10693', '0.2566', '-0.1353', '-0.4521', '0.417', '0.1324', '0.4219', '-0.4856', '0.2372', '0.5254', '0.5054', '-0.2303', '-0.574', '0.8433', '0.241', '0.356', '0.1552', '0.1989', '0.3667', '-0.3677', '-0.8906', '0.3987', '0.64', '-0.3213', '-0.2734', '0.1902', '-0.09125', '0.578', '0.5806', '0.4094', '0.6577', '-0.0633', '0.0928', '1.007', '0.782', '0.542', '0.427', '0.10596', '-0.0822']",,,C537206,,,,
mondo:0007299,Sotos syndrome 1,"['Sotos syndrome caused by mutation in NSD1', 'Sotos syndrome 1', 'chromosome 5q35 deletion syndrome', 'SOTOS1', 'Sotos syndrome', 'Sotos syndrome type 1', 'NSD1 Sotos syndrome', 'cerebral gigantism']",0112103,117550,,CN035106,,,,,,,,
mondo:0007300,cerebral sarcoma,"['sarcoma of telencephalon', 'telencephalon sarcoma', 'cerebral sarcoma']",,117600,,C1861714,,,,C537946,,,,
mondo:0007301,cerebrocostomandibular syndrome,"['CEREBROCOSTOMANDIBULAR syndrome', 'rib Gap defects with micrognathia', 'cerebro-costo-mandibular syndrome', 'CCM syndrome', 'CCMS', 'cerebrocostomandibular syndrome']",0111248,117650,1393,C0265342,"['-0.479', '0.574', '-0.155', '-0.652', '0.3403', '-0.2944', '0.0102', '0.754', '-0.4937', '-0.945', '-0.4016', '-0.6226', '0.04617', '0.4587', '-0.773', '-0.3975', '0.5757', '-0.5776', '-0.629', '-0.4287', '0.0995', '0.3215', '0.661', '-0.2408', '-0.1947', '0.01414', '-0.3462', '0.1945', '0.3318', '-0.03638', '-0.37', '-0.11566', '0.1953', '0.7', '-0.2664', '-0.1007', '0.2167', '-0.0523', '-0.252', '0.2598', '0.451', '0.02893', '-0.8237', '-0.1368', '-0.1647', '0.10535', '-0.2404', '0.3193', '-0.1353', '1.004', '-0.266', '-0.525', '0.1342', '-0.1382', '-0.0627', '0.2646', '0.2058', '0.5005', '0.3918', '0.746', '0.066', '0.1159', '-0.5317', '0.03433', '-0.285', '-0.3457', '0.0543', '0.0869', '-0.8496', '0.3225', '0.1921', '-0.3403', '-0.1702', '-0.55', '0.3308', '-0.1294', '0.3208', '-0.4126', '-0.504', '-0.01119', '-0.1134', '0.01622', '0.3533', '0.597', '-0.2046', '0.65', '0.1694', '0.2156', '-0.02252', '0.02287', '-0.2095', '0.0705', '-0.347', '0.9644', '0.7017', '-0.06665', '0.264', '-0.3235', '0.692', '0.276']",,,C562538,759.89,,,
mondo:0007302,cervical hypertrichosis with underlying kyphoscoliosis,"['cervical hypertrichosis with underlying kyphoscoliosis', 'hypertrichosis, posterior cervical, with underlying kyphoscoliosis']",,117850,,C1861695,,,,C566142,,,,
mondo:0007303,cervical rib disease,"['cervical rib syndrome', 'cervical rib']",,117900,,,,C158329,1000861,D002573,756.2,,10008301,0000891
mondo:0007304,cervical vertebral Bridge,['cervical vertebral Bridge'],,118000,,,,,,,,,,
mondo:0007305,cervical vertebral dysplasia,"['cervical vertebral dysplasia (disease)', 'cervical vertebral dysplasia']",,118005,,C1861693,,,,C566140,,,,0008469
mondo:0007306,"Klippel-Feil syndrome 1, autosomal dominant","['Klippel-Feil syndrome 1, autosomal dominant', 'GDF6 isolated Klippel-Feil syndrome', 'cervical vertebral fusion, autosomal dominant', 'Klippel-FEIL syndrome 1, autosomal dominant', 'KFS1', 'isolated Klippel-Feil syndrome caused by mutation in GDF6', 'Kfs']",0080589,118100,,C1861689,,,,C536887,,,,
mondo:0007307,Charcot-Marie-Tooth disease type 1B,"['Charcot-Marie-Tooth disease type 1 caused by mutation in MPZ', 'HMSN1B', 'MPZ Charcot-Marie-Tooth disease type 1', 'Charcot-Marie-Tooth disease slow nerve conduction type linked to Duffy', 'HMSN 1B', 'Charcot-Marie-Tooth disease, demyelinating, type 1B', 'Charcot-Marie-Tooth disease, slow nerve conduction type, linked to Duffy', 'Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1B', 'CMT1B', 'autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B', 'hereditary motor and sensory neuropathy 1', 'HMSN1', 'HMSN IB', 'Charcot-Marie-Tooth neuropathy type 1B', 'CMT 1B', 'hereditary motor and sensory neuropathy IB', 'Charcot-Marie-Tooth neuropathy, type 1B', 'Charcot-Marie-Tooth disease, type 1B', 'hereditary motor and sensory neuropathy 1B', 'Charcot Marie Tooth disease type 1B']",0110152,118200,101082,C0270912,"['0.2474', '0.3008', '0.1492', '-0.052', '0.2576', '0.01817', '-0.2832', '0.643', '-0.7256', '-0.1216', '-0.037', '0.1572', '-0.6914', '0.2578', '0.01653', '-0.3733', '-0.4753', '-0.918', '-0.1985', '-0.11847', '0.317', '0.3162', '0.2993', '0.3474', '0.2651', '0.3762', '-0.0813', '-0.1499', '0.2124', '-0.2329', '0.10925', '-0.2534', '0.2347', '-0.02716', '0.2446', '-0.682', '-0.576', '-0.2362', '0.3538', '0.1122', '-1.11', '-0.5737', '-0.3826', '0.05225', '0.1423', '0.04224', '0.1797', '-0.0763', '-0.013596', '-0.05975', '0.3079', '0.1843', '-0.5723', '-1.008', '0.1602', '-0.1436', '0.1099', '0.05', '-0.6006', '-0.3132', '-0.3005', '0.0894', '0.2106', '0.739', '-0.541', '1.317', '-0.3987', '0.589', '-0.505', '0.09283', '-0.4573', '0.11865', '0.5566', '-0.407', '1.193', '0.748', '-0.3992', '0.241', '0.2742', '-0.4958', '0.416', '-0.243', '0.793', '0.5757', '0.09576', '0.006035', '0.6294', '0.551', '0.4397', '0.3489', '0.1708', '-0.04623', '-0.001874', '0.1748', '0.6343', '0.7095', '0.695', '-0.843', '-0.1364', '0.394']",C118782,,,,,,
mondo:0007308,Charcot-Marie-Tooth disease type 2A1,"['Charcot-Marie-Tooth disease, neuronal, type 2A', 'hereditary motor and sensory neuropathy IIA1', 'Charcot-Marie-Tooth disease, type 2A1', 'Charcot-Marie-Tooth disease, axonal, type 2A', 'hereditary motor and sensory neuropathy 2 A', 'Charcot-Marie-Tooth disease, axonal, autosomal dominant, type 2A1', 'Charcot-Marie-Tooth neuropathy, type 2A1', 'autosomal dominant Charcot-Marie-Tooth disease axonal type 2A1', 'CMT2A', 'KIF1B Charcot-Marie-Tooth disease type 2', 'Charcot-Marie-Tooth disease neuronal type 2A1', 'CMT2A1', 'HMSN IIA', 'hereditary motor and sensory neuropathy IIa1', 'Charcot-Marie-Tooth disease, axonal, type 2A1', 'Charcot-Marie-Tooth disease, neuronal, type 2A1', 'CMT 2A', 'HMSN2A1', 'Charcot Marie Tooth disease type 2A', 'autosomal dominant Charcot-Marie-Tooth disease type 2A1', 'HMSN IIa1', 'Charcot-Marie-Tooth disease type 2A', 'Charcot-Marie-Tooth neuropathy type 2A1', 'Charcot-Marie-Tooth disease type 2 caused by mutation in KIF1B', 'HMSN IIA1']",0110154,118210,99946,,"['0.1987', '0.4038', '-0.02797', '-0.3298', '0.0451', '-0.3123', '0.0823', '0.7344', '-0.6567', '-0.11096', '0.2349', '0.3325', '-0.4155', '0.4185', '-0.1317', '-0.006733', '-0.2634', '-0.6255', '-0.447', '-0.4358', '0.04715', '0.3633', '0.10455', '0.514', '0.4758', '0.4084', '0.2235', '0.03394', '0.2593', '0.0187', '0.09314', '-0.44', '0.1827', '-0.168', '0.2272', '-0.639', '-0.3816', '-0.0989', '0.468', '-0.329', '-1.327', '-0.4539', '-0.3662', '0.3462', '-0.299', '-0.1387', '0.02608', '-0.09033', '0.04904', '-0.1171', '-0.006237', '0.2156', '-0.2947', '-0.9', '0.1812', '-0.2404', '0.3145', '0.2054', '-0.5103', '-0.11145', '-0.2632', '0.2607', '0.679', '0.4504', '-0.8325', '1.133', '-0.2886', '0.4246', '-0.696', '0.4187', '-0.611', '0.3281', '0.3918', '-0.0478', '0.8403', '0.716', '-0.3894', '0.369', '0.0687', '-0.3708', '0.005165', '-0.2477', '0.7915', '0.6045', '0.2339', '0.0759', '0.163', '0.6787', '0.7334', '0.4814', '0.09973', '-0.3245', '0.1121', '0.2439', '0.7964', '0.737', '0.6343', '-0.617', '-0.2817', '0.4292']",C150609,,C566138,,,,
mondo:0007309,Charcot-Marie-Tooth disease type 1A,"['HMSN1A', 'HMSN 1A', 'Charcot-Marie-Tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1A', 'Charcot-Marie-Tooth neuropathy, type 1A', 'Charcot-Marie-Tooth disease, type 1A', 'Charcot Marie Tooth disease type 1A', 'Charcot-Marie-Tooth syndrome type 1A', 'Charcot-Marie-Tooth disease, demyelinating, type 1A', 'CMT1A', 'microduplication 17p12', 'hereditary motor and sensory neuropathy 1A', 'CMT 1A', 'autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1A', 'Charcot-Marie-Tooth neuropathy type 1A']",0110148,118220,101081,C0270911,"['0.3418', '0.2068', '0.193', '-0.0967', '-0.1028', '-0.1415', '-0.2235', '0.4338', '-0.769', '-0.573', '0.0693', '-0.0237', '0.04132', '0.9326', '-0.3188', '-0.2876', '-0.1343', '-0.6177', '-0.5737', '-0.3162', '0.1501', '-0.03253', '0.3818', '0.5854', '0.0672', '0.1188', '0.1444', '0.387', '0.4111', '-0.1422', '0.09314', '-0.5254', '0.0673', '-0.09827', '0.1654', '-0.6343', '0.0122', '-0.2905', '0.578', '-0.1548', '-1.165', '-0.1984', '-0.3362', '0.4749', '-0.06046', '-0.4326', '0.2124', '0.07196', '-0.03537', '0.0595', '-0.1621', '-0.1245', '-0.02885', '-1.316', '0.0873', '-0.1635', '0.4207', '0.61', '-0.5107', '-0.08356', '-0.3499', '0.04706', '0.632', '0.4468', '-0.7773', '1.201', '0.10846', '0.187', '-0.6753', '0.03482', '-0.741', '-0.2222', '0.1874', '-0.4314', '1.247', '0.497', '-0.597', '0.3372', '-0.0428', '-0.6406', '0.3503', '-0.2223', '0.6533', '0.639', '-0.3179', '-0.203', '0.1777', '0.4316', '0.5527', '0.6064', '-0.3145', '-0.0699', '0.05768', '0.1733', '0.611', '0.05722', '0.4304', '-0.569', '-0.1886', '0.464']",C75468,,,,,,
mondo:0007310,"Charcot-Marie-Tooth disease, Guadalajara neuronal type","['Charcot-Marie-Tooth disease, Guadalajara neuronal type']",,118230,,C1861673,,,,C566137,,,,
mondo:0007311,Charcot-Marie-Tooth disease type 1E,"['Charcot Marie Tooth disease type 1E', 'Charcot-Marie-Tooth disease-deafness', 'Charcot-Marie-Tooth disease, demyelinating, type 1E', 'Charcot-Marie-Tooth disease and deafness', 'Charcot-Marie-Tooth disease demyelinating type 1E', 'Charcot-Marie-Tooth disease-deafness syndrome', 'Charcot-Marie-Tooth neuropathy and deafness, autosomal dominant', 'autosomal dominant Charcot-Marie-Tooth neuropathy and deafness', 'CMT 1E', 'Charcot-Marie-Tooth disease, type 1E', 'CMT1E']",0110153,118300,90658,C2931686,"['0.04886', '0.2415', '0.1051', '0.2725', '-0.1251', '-0.383', '0.08', '0.402', '-0.5596', '-0.10095', '0.107', '0.4504', '-0.1486', '0.4917', '0.1334', '-0.3306', '-0.2025', '-0.449', '-0.42', '-0.6304', '0.317', '0.4512', '0.3086', '0.654', '0.4182', '0.3376', '0.0926', '0.3726', '0.1942', '-0.1371', '0.3035', '-0.743', '0.007904', '0.2695', '0.1008', '-0.5537', '-0.486', '-0.348', '0.2622', '-0.10376', '-1.326', '-0.3237', '-0.2307', '0.2299', '0.1273', '-0.03091', '0.2559', '-0.08636', '-0.2856', '0.373', '0.2146', '0.2803', '-0.611', '-1.07', '0.01956', '0.01079', '-0.03644', '0.4016', '-0.599', '-0.08496', '-0.1804', '0.0636', '0.399', '0.361', '-0.714', '0.9917', '-0.2352', '0.517', '-0.5405', '0.1982', '-0.547', '0.01987', '0.617', '-0.1648', '1.122', '0.6333', '-0.0926', '0.519', '-0.1404', '-0.5903', '0.01709', '-0.3325', '0.521', '0.82', '0.3735', '-0.2299', '0.2769', '0.48', '0.5825', '0.4524', '0.3674', '0.1104', '-0.004826', '0.3342', '0.396', '0.4695', '0.281', '-0.639', '-0.10175', '0.3994']",,,C537986,,,,
mondo:0007312,Charcot-Marie-Tooth disease with ptosis and parkinsonism,['Charcot-Marie-Tooth disease with ptosis and parkinsonism'],,118301,,C1861668,,,,C538079,,,,
mondo:0007313,cheilitis glandularis,['cheilitis glandularis'],,118330,1221,C0267034,,,,C535921,,,,
mondo:0007314,"chemodectoma, intraabdominal, with cutaneous angiolipomas","['chemodectoma, intraabdominal, with cutaneous angiolipomas', 'abdominal chemodectomas with cutaneous angiolipomas']",,118350,,C2930928,,,,C535552,,,,
mondo:0007315,cherubism,"['cherubism', 'familial multilocular cystic disease of the jaws', 'Crbm', 'familial fibrous dysplasia of the jaws', 'CRBM']",1856,118400,184,C0008029,"['-0.01426', '0.1282', '-0.0488', '0.0739', '0.1142', '-0.03128', '0.67', '0.2108', '-0.78', '-0.03003', '-0.6777', '-0.207', '-0.1257', '0.5723', '0.6187', '0.138', '0.03317', '-0.1466', '-0.1746', '-0.388', '-0.4954', '0.01518', '0.8975', '-0.3523', '0.2512', '0.04623', '-0.0856', '0.02637', '0.524', '-0.0485', '0.3215', '0.1412', '-0.1423', '0.2231', '0.462', '0.2524', '0.011284', '-0.2261', '0.515', '0.0394', '0.969', '0.2418', '0.07214', '0.01251', '0.598', '-0.00935', '-0.03925', '0.0572', '0.0917', '0.0424', '0.119', '0.4822', '-0.223', '-0.1411', '-0.5127', '0.313', '0.01382', '-0.2712', '0.2668', '0.2418', '0.4353', '0.2424', '0.01319', '-0.2705', '0.0462', '-0.282', '0.5566', '1.018', '-0.1266', '0.3853', '0.3657', '-0.2734', '0.2268', '-0.4868', '-0.0589', '-0.2231', '-0.0244', '-0.1586', '0.02884', '-0.5786', '-0.1603', '-0.1938', '0.12006', '0.573', '-0.001143', '-0.2683', '0.4683', '-0.3286', '0.443', '0.2272', '-0.169', '0.2766', '-0.3047', '0.8896', '0.5625', '-0.4568', '0.4265', '-0.7764', '0.129', '0.7397']",C84630,,D002636,526.89,,10070535,
mondo:0007316,Chiari malformation type I,"['Chiari malformation type I', 'Chiari malformation type 1', 'Arnold-Chiari malformation type I', 'Cm1', 'Cm1 with syringomyelia', 'Arnold-Chiari malformation type 1', 'Chiari malformation type 1 with syringomyelia']",,118420,268882,,,,,,,,10056944,
mondo:0007318,Alagille syndrome,"['Cardiovertebral syndrome', 'Alagille-Watson syndrome', 'Watson Alagille syndrome', 'hepatic ductular hypoplasia', 'Alagille syndrome', 'paucity of interlobular bile ducts', 'Arteriohepatic dysplasia', 'syndromic bile duct paucity', 'Hepatofacioneurocardiovertebral syndrome', 'Watson-Miller syndrome']",9245,,52,C0085280,"['-0.1176', '0.2703', '0.5015', '-1.007', '-0.03735', '0.11993', '-0.1785', '0.4485', '-0.1908', '-0.09906', '-0.625', '-0.01802', '-0.06274', '0.1547', '-1.177', '-0.5986', '0.1892', '-0.1156', '0.3376', '-0.4084', '0.4924', '-0.4502', '0.408', '0.12213', '-0.5146', '0.2888', '0.14', '0.11597', '1.2705', '0.04492', '0.3481', '-0.2773', '0.3306', '0.1248', '-0.02673', '-0.3535', '-0.1055', '-0.485', '0.2773', '-0.1658', '-0.3403', '-0.03812', '0.742', '0.3704', '-0.3767', '0.0434', '0.5044', '0.549', '0.1101', '-0.1675', '-0.06616', '0.243', '-0.1399', '-0.3423', '-0.525', '-0.6416', '0.449', '0.1642', '0.0241', '0.3516', '0.301', '-0.01816', '-0.01182', '-0.4941', '0.1305', '0.10944', '0.509', '0.8125', '-0.2996', '0.3923', '-0.509', '0.1957', '0.4385', '0.3057', '0.04343', '0.08234', '0.8066', '-0.715', '-0.2537', '-0.07684', '-0.03424', '-0.2607', '-0.5576', '-0.04605', '-0.403', '0.3645', '0.2148', '0.3813', '0.2583', '-0.2356', '0.296', '0.3992', '0.176', '0.09717', '0.72', '-0.2556', '0.2522', '-0.5293', '0.2957', '0.1799']",C35139,,D016738,759.89,,10053870,
mondo:0007319,chondrocalcinosis 2,"['chondrocalcinosis 2', 'calcium pyrophosphate arthropathy', 'calcium pyrophosphate dihydrate deposition disease', 'calcium gout', 'chondrocalcinosis familial articular', 'familial calcium pyrophosphate dihydrate deposition disease', 'familial calcium pyrophosphate deposition', 'calcium pyrophosphate dihydrate crystal deposition disease', 'familial CC', 'hereditary articular chondrocalcinosis', 'calcium pyrophosphate arthropathy, familial', 'chondrocalcinosis, familial articular', 'hereditary CC', 'CPPDD', 'hereditary calcium pyrophosphate deposition', 'familial articular chondrocalcinosis', 'Pseudogout, familial', 'CCAL2', 'chondrocalcinosis type 2', 'familial CPPD', 'calcium gout, familial']",,118600,1416,CN199517,,,,C563162,,,,
mondo:0007320,chondrocalcinosis due to apatite crystal deposition,"['chondrocalcinosis due to apatite crystal deposition', 'familial apatite disease']",,118610,,C1861580,,,,C535939,,,,
mondo:0007321,autosomal dominant chondrodysplasia punctata,"['chondrodysplasia punctata, Sheffield type', 'chondrodysplasia punctata due to warfarin teratogenicity', 'chondrodysplasia punctata, autosomal dominant', 'chondrodysplasia punctata due to vitamin K deficiency']",0060293,118650,79344,,,,,C563248,,,,
mondo:0007322,"chondrodysplasia punctata, tibial-metacarpal type","['chondrodysplasia punctata, Mt type', 'chondrodysplasia punctata, tibia-metacarpal type']",,118651,79346,,,,,C562961,756.59,,,
mondo:0007323,Chondronectin,['Chondronectin'],,118670,,,,,,,,,,
mondo:0007325,"choreoathetosis, familial inverted","['infantile choreoathetosis of Fisher', 'choreoathetosis, familial inverted']",,118750,,C1861569,,,,C566127,,,,
mondo:0007327,"chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase","['hyperlipoproteinemia, type 1C', 'chylomicronemia, familial, due to circulating inhibitor of lipoprotein lipase']",0111419,118830,411,C1861560,"['-0.009026', '0.0569', '0.01048', '-0.01472', '0.0338', '-0.06076', '0.00458', '0.06506', '-0.05646', '-0.0072', '-0.0416', '-0.005173', '0.01567', '0.00471', '-0.02074', '-0.03677', '0.01524', '-0.03357', '0.006786', '-0.0845', '-0.004177', '-0.03745', '0.0646', '-0.008224', '0.006138', '-0.007145', '-0.00751', '-0.02516', '0.006172', '-0.01823', '0.05765', '0.001003', '0.06256', '0.01675', '0.010345', '-0.02776', '-0.02322', '-0.02293', '-0.005802', '-0.04135', '0.03018', '-0.06537', '0.0317', '0.002684', '-0.0217', '-0.04868', '-0.00895', '0.04974', '0.0222', '0.01026', '0.006046', '-0.01202', '0.00887', '-0.0292', '-0.03455', '-0.02583', '0.0558', '-0.0531', '-0.06024', '0.01148', '0.007362', '0.02936', '0.02454', '-0.012245', '0.00864', '0.01996', '0.058', '0.0275', '-0.0582', '0.05167', '-0.03656', '-0.004883', '0.01352', '-0.04282', '0.03305', '0.0476', '-0.02512', '0.0055', '-0.06055', '-0.0392', '-0.0009394', '0.004047', '-0.01569', '0.01354', '-0.01587', '0.01345', '0.01924', '0.07587', '0.06775', '0.00531', '0.01384', '0.05313', '0.02415', '-0.013374', '0.1005', '0.05365', '0.04843', '-0.0841', '-0.02354', '0.009125']",,,C566126,,,,
mondo:0007328,"choroidal osteoma, bilateral","['choroidal osteoma, bilateral']",,118865,,C1861558,,,,C566124,,,,
mondo:0007329,"cirrhosis, familial","['endemic Tyrolean infantile cirrhosis', 'hereditary cirrhosis of liver', 'cirrhosis, Noncryptogenic, susceptibility to', 'cryptogenic cirrhosis', 'copper-overload cirrhosis', 'Sen syndrome', 'cirrhosis, familial, with pulmonary hypertension', 'Indian childhood cirrhosis', 'copper toxicosis, idiopathic', 'cirrhosis, familial', 'cirrhosis, cryptogenic']",,215600,209919,,"['0.002123', '0.0322', '-0.00397', '-0.007652', '0.02621', '-0.0572', '-0.0026', '0.0441', '-0.02586', '-0.01106', '-0.00687', '-0.02257', '-0.003145', '0.02638', '-0.03238', '-0.0382', '-0.006844', '-0.002806', '-0.003662', '-0.0756', '0.001737', '-0.01593', '0.04492', '-0.0322', '0.007504', '-0.003975', '0.01394', '-0.009125', '0.01296', '-0.03214', '0.05518', '-0.01482', '0.04642', '0.01802', '0.004147', '-0.01958', '-0.03467', '-0.0188', '-0.01171', '-0.03305', '0.02031', '-0.02982', '0.02408', '-0.01688', '0.0001438', '-0.02478', '-0.0188', '0.02133', '-0.003426', '0.01329', '-0.01298', '0.01726', '0.011185', '0.02063', '-0.00518', '-0.0211', '0.02525', '-0.02466', '-0.06555', '-0.01831', '0.02869', '0.02502', '0.005196', '-0.01283', '-0.0009184', '0.007492', '0.0576', '0.03665', '-0.05814', '0.05658', '-0.01768', '-0.002438', '0.02043', '-0.02397', '0.02443', '0.02701', '0.0002794', '0.007004', '-0.03102', '-0.02257', '-0.01145', '0.008316', '-0.02698', '0.02087', '-0.002804', '-0.006725', '0.01448', '0.02827', '0.05542', '-0.004734', '0.01294', '0.01662', '-0.002626', '-0.001201', '0.09314', '0.03333', '0.051', '-0.06366', '-0.02748', '0.006424']",C84411,,C566123,,,,
mondo:0007330,congenital pseudoarthrosis of clavicle,"['clavicle, pseudarthrosis of, congenital', 'congenital pseudarthrosis of the clavicle', 'congenital pseudoarthrosis of the clavicle']",,118980,66630,,,,,C562548,,,,
mondo:0007332,split-hand/foot malformation with long bone deficiency 1,"['tibial aplasia with split-hand-split-foot deformity', 'ectrodactyly with aplasia of long bones', 'aplasia of tibia with ectrodactyly', 'cleft hand and absent tibia', 'split-hand/foot malformation with long bone deficiency', 'split-hand/foot malformation with long bone deficiency 1', 'cleft hand absent tibia', 'SHFLD1', 'tibial aplasia with split-hand/split-foot deformity', 'SHFLD', 'split-hand-foot malformation with long bone deficiency']",,119100,,,,,,C536425,,,,
mondo:0007333,van der Woude syndrome 1,"['lip-pit syndrome', 'VAN DER Woude syndrome 1', 'cleft lip and/or palate with mucous cysts of Lower lip', 'IRF6 van der Woude syndrome', 'van der Woude syndrome 1', 'Vdws', 'Van Der Woude syndrome type 1', 'VWS1', 'van der Woude syndrome caused by mutation in IRF6']",,119300,,,,,,,,,,
mondo:0007334,autosomal dominant popliteal pterygium syndrome,"['cleft lip/palate paramedian mucous cysts of the lower lip popliteal pterygium digital and genital anomalies', 'popliteal pterygium syndrome, autosomal dominant', 'popliteal pterygium syndrome 1', 'cleft Lip/palate, paramedian mucous cysts of the Lower Lip, popliteal pterygium, digital and genital anomalies', 'popliteal pterygium syndrome', 'popliteal web syndrome', 'faciogenitopopliteal syndrome', 'facio-genito-popliteal syndrome', 'PPS']",,119500,1300,CN199177,"['0.579', '-0.2664', '0.433', '-0.678', '0.762', '-0.7427', '0.1677', '1.036', '-0.866', '-0.6865', '0.0018015', '-0.507', '-0.146', '0.47', '0.3135', '0.2234', '0.3218', '-0.8535', '-0.5327', '-0.638', '-0.0563', '-0.03433', '0.3098', '-0.03754', '0.1748', '0.2247', '-0.2747', '0.1356', '0.4688', '-0.443', '0.699', '-0.6504', '-0.04724', '0.01994', '-0.583', '-0.1522', '0.0421', '-0.199', '0.2654', '0.00673', '0.5005', '-0.0316', '0.4543', '-0.1313', '-0.0497', '-0.3794', '-0.2156', '0.4087', '0.1813', '-0.2178', '-0.9263', '-0.4324', '-0.5874', '-0.1282', '-1.004', '-0.0886', '0.693', '0.04514', '-0.271', '0.07104', '0.507', '0.804', '-0.1985', '0.6265', '0.125', '0.3108', '0.08813', '-0.1201', '0.2494', '0.2395', '-0.351', '-0.09216', '-0.2944', '-0.1726', '0.5186', '0.4573', '0.04047', '-0.1774', '-0.8745', '-0.377', '-0.0897', '0.186', '0.934', '0.4485', '-0.1192', '0.4202', '-0.5264', '0.4504', '-0.4304', '0.396', '-0.1389', '0.4905', '-0.01169', '0.5376', '0.3997', '-0.575', '0.2957', '-0.2039', '0.3823', '0.2798']",,,,,,,
mondo:0007335,orofacial cleft 1,"['orofacial cleft-1', 'cleft Lip/palate, nonsyndromic', 'orofacial cleft 1', 'orofacial cleft, nonsyndromic', 'OFC1', 'cleft lip with or without cleft palate, nonsyndromic, 1']",0080395,119530,,C1861537,,C124838,,C566121,,,,
mondo:0007336,isolated cleft palate,"['dominant cleft palate', 'nonsyndromic cleft palate', 'CPI', 'cleft palate, isolated', 'cleft palate']",0110213,119540,,CN234898,"['-0.01031', '0.01935', '0.00707', '-0.003899', '0.00906', '-0.02086', '0.002127', '0.03503', '-0.01447', '-0.0281', '0.0006537', '-0.002266', '0.00454', '0.00467', '-0.0186', '-0.01715', '0.00827', '-0.02632', '-0.0237', '-0.05896', '-0.001272', '-0.004097', '0.0351', '-0.001119', '0.0163', '0.004723', '-0.01128', '0.00478', '0.02063', '-0.012085', '0.0108', '0.0002646', '0.04102', '0.006794', '0.00812', '-0.00447', '0.00446', '-0.01112', '0.001779', '-0.0391', '0.00941', '-0.02727', '-0.001765', '-0.0199', '-0.01695', '-0.02443', '-0.000317', '0.01903', '0.00368', '0.0129', '-0.01265', '-0.02098', '0.00552', '-0.006954', '-0.01834', '-0.02097', '0.0243', '-0.0131', '-0.03616', '0.007042', '0.02449', '0.01272', '-0.01016', '0.0008864', '-0.0144', '0.0035', '0.02167', '0.0323', '-0.02852', '0.02922', '-0.032', '-0.000565', '0.02177', '-0.02696', '0.01094', '0.01442', '0.01502', '-0.01826', '-0.02133', '-0.01917', '-0.010735', '0.007088', '-9.9e-05', '0.03137', '-0.01349', '0.011734', '-0.005062', '0.02081', '0.0359', '0.009315', '0.00199', '0.02647', '0.00266', '0.002508', '0.064', '0.001563', '0.01715', '-0.02304', '0.0105', '0.01525']",,,,,Q35.3,,
mondo:0007337,cleft palate-lateral synechia syndrome,"['cleft palate-lateral synechia syndrome', 'CPLS syndrome', 'Cpls syndrome', 'cleft palate lateral synechia syndrome', 'syngnathia']",0080313,119550,2016,C0795898,,,,C563047,759.89,,,
mondo:0007338,cleft soft palate,"['cleft soft palate', 'soft cleft palate', 'cleft velum', 'cleft velum palatinum']",0110214,119570,99772,,,,,C562950,,Q35.3,,
mondo:0007339,blepharocheilodontic syndrome,"['blepharo-cheilo-odontic syndrome', 'lagophthalmia-cleft lip and palate syndrome', 'clefting, ectropion, and conical teeth', 'lagophthalmia with bilateral cleft lip and palate', 'Elsching syndrome', 'clefting-ectropion-conical teeth syndrome', 'BCD syndrome', 'ectropion inferior-cleft lip and/or palate syndrome', 'BCDS', 'BCDS1', 'blepharo-cheilo-dontic syndrome', 'Elschnig syndrome', 'blepharocheilodontic syndrome 1', 'ectropion, inferior, with cleft lip and/or palate', 'ectropion inferior cleft lip and or palate', 'ectropion inferior-cleft lip and or palate syndrome', 'blepharocheilodontic syndrome']",0080344,,1997,C1861536,"['0.581', '0.01113', '0.04086', '-0.0988', '0.238', '-0.12115', '0.3032', '0.958', '-0.2573', '-0.7617', '-0.1803', '-0.442', '-0.1008', '0.2786', '-0.2157', '0.206', '-0.08215', '-0.505', '-0.3127', '-0.8345', '-0.2156', '-0.2249', '0.03732', '-0.5522', '0.427', '0.4465', '-0.2976', '0.4668', '1.213', '-0.3184', '0.414', '0.3406', '-0.1593', '-0.0203', '-0.06088', '-0.2244', '0.3792', '-0.3525', '0.407', '-0.2708', '0.3418', '-0.2075', '-0.08203', '-0.6562', '0.4138', '-0.05347', '0.2546', '-0.079', '0.0614', '-0.3794', '-0.375', '0.4268', '0.3093', '0.1014', '-1.123', '-0.6177', '0.0417', '-0.554', '-0.4695', '-0.411', '0.5513', '-0.1283', '-0.0476', '0.0911', '-0.3408', '0.1329', '0.4321', '0.1236', '0.09924', '0.112', '-0.1398', '0.1442', '-0.2598', '0.4302', '0.836', '-0.07605', '0.0681', '-0.5547', '0.0886', '0.4812', '-0.03232', '0.2622', '0.648', '0.879', '-0.1803', '0.0227', '0.1458', '0.4697', '0.514', '0.03558', '0.1919', '0.5244', '-0.1186', '0.07794', '1.205', '-0.801', '0.0681', '-0.2203', '-0.04034', '0.361']",,,C536188,,,,
mondo:0007340,cleidocranial dysplasia 1,"['cleidocranial dysplasia, forme fruste, dental anomalies only', 'CCD', 'cleidocranial dysplasia, forme fruste, with brachydactyly', 'cleidocranial dysplasia', 'CLCD', 'dysplasia cleidocranial', 'Marie-Sainton disease', 'cleidocranial dysostosis']",13994,119600,1452,C0008928,"['-0.2595', '-0.068', '0.3884', '-0.414', '0.532', '0.361', '0.2937', '1.153', '-0.684', '-0.1581', '-0.255', '-0.3418', '-0.0968', '0.692', '0.1796', '0.5347', '0.5176', '0.3564', '-0.8237', '-0.5396', '-0.3574', '-0.0979', '0.619', '0.1159', '0.2659', '-0.1907', '-0.3394', '0.256', '0.0971', '-0.6987', '0.3794', '-0.2766', '-0.2465', '0.0714', '0.4133', '-0.3477', '0.00462', '-0.5596', '0.2615', '-0.6846', '0.1648', '0.4429', '0.1013', '-0.687', '0.2379', '-0.55', '0.189', '-0.01517', '-0.2947', '0.4187', '0.2583', '0.1602', '-0.0579', '-0.2303', '-0.33', '-0.525', '-0.2109', '-0.2595', '0.2756', '-0.4294', '0.10187', '0.4844', '-0.2666', '-0.1288', '0.3208', '-0.005272', '-0.1414', '0.0696', '-0.07837', '0.298', '0.08276', '-0.314', '-0.0723', '-0.03088', '0.0489', '0.2302', '0.729', '0.3245', '0.04254', '-0.6562', '-0.31', '-0.06204', '0.0542', '0.72', '-0.15', '0.0924', '-0.04468', '0.05725', '0.06445', '0.3242', '-0.8', '-0.09235', '-0.721', '0.5273', '0.7754', '0.4075', '0.7437', '-0.3972', '0.819', '-0.1271']",C75020,,D002973,755.59,,,
mondo:0007341,cleidorhizomelic syndrome,"['Wallis-Zieff-Goldblatt syndrome', 'rhizomelic shortness with clavicular defect', 'cleido rhizomelic syndrome', 'brachydactyly, enlarged diaphysis, rhizomelic micromelia, short stature and abnormal clavicle', 'Wallis Zieff Goldblatt syndrome', 'cleidorhizomelic syndrome']",,119650,1453,C1861515,,,,C536428,,,,
mondo:0007342,clubfoot,"['talipes', 'clubfoot, congenital, with or without deficiency of long bones and/or mirror-IMAGE polydactyly', 'equinovarus deformity of foot', 'congenital equinovarus', 'CCF', 'congenital talipes equinovarus', 'club foot', 'congenital clubfoot', 'clubbed foot', 'equinovarus deformity of foot (finding)', 'talipes equinovarus']",11836,119800,,,"['-0.0003004', '0.002998', '0.01182', '0.005577', '0.00957', '-0.01898', '0.003166', '0.02263', '-0.01973', '-0.012344', '-0.01155', '0.005943', '-0.009445', '0.004368', '0.001598', '-0.011536', '-0.006557', '-0.01112', '-0.01587', '-0.01217', '-0.002285', '-0.00537', '0.002272', '0.004494', '0.00919', '-0.00299', '0.0082', '0.004032', '-0.00401', '-0.01376', '0.00885', '-0.01416', '-0.001272', '0.00761', '-0.006382', '-0.01103', '-0.006107', '-0.01598', '0.00949', '-0.002495', '0.009766', '-0.004063', '-0.002594', '-0.00606', '0.000913', '0.002975', '0.002377', '0.007576', '0.006924', '-0.001221', '-0.01176', '-0.005646', '-0.006413', '-0.00419', '-0.01346', '-0.00824', '0.002083', '-0.002195', '-0.009926', '-0.003773', '0.00407', '0.006557', '0.002893', '-0.0007834', '-0.00691', '-0.002615', '0.01228', '0.012436', '0.002005', '0.01145', '-0.004787', '-0.00024', '-0.003391', '-0.01564', '0.006397', '0.010735', '-0.00342', '0.003027', '-0.00936', '0.001521', '-0.005386', '0.005344', '-0.0003736', '0.01548', '0.0007763', '-0.00555', '0.00817', '0.006794', '0.01892', '0.00895', '-0.0004075', '0.01013', '-0.005703', '0.00435', '0.01425', '0.0006285', '0.00853', '-0.01052', '0.002048', '-0.003128']",C84641,,D003025,754.51,,,
mondo:0007343,isolated congenital digital clubbing,"['clubbing of digits', 'isolated congenital nail clubbing', 'acropachy, hereditary', 'digital clubbing, isolated congenital', 'isolated congenital acropachy']",,119900,217059,,"['-0.2544', '-0.322', '-0.03583', '-0.10956', '0.5635', '-0.03525', '0.07416', '0.385', '-0.4187', '-0.2542', '0.0664', '0.1626', '-0.2522', '0.2827', '0.07745', '0.1294', '0.5845', '-0.5854', '-0.2317', '-0.8726', '-0.2544', '0.1268', '0.599', '-0.2986', '0.6294', '0.0963', '-0.06836', '0.2908', '0.07324', '-0.05353', '0.346', '-0.3108', '-0.1211', '0.3179', '-0.1512', '0.0429', '-0.04367', '-0.0787', '0.03824', '-0.0946', '0.2947', '-0.2329', '0.2015', '-0.0005984', '0.0993', '-0.09186', '-0.1422', '0.2644', '0.04883', '0.1958', '-0.1323', '0.02151', '-0.04266', '-0.2178', '-0.6084', '-0.348', '0.2036', '-0.1431', '-0.4204', '-0.2522', '0.2484', '0.006798', '-0.1527', '0.1026', '-0.426', '0.2515', '0.4724', '0.5435', '-0.0788', '0.1572', '-0.3967', '0.1855', '0.1874', '-0.1415', '0.094', '-0.05066', '0.1478', '0.04132', '-0.4355', '-0.4658', '-0.1846', '0.0968', '0.44', '-0.04407', '-0.0698', '-0.3213', '-0.2069', '-0.02191', '-0.02496', '-0.1464', '-0.2874', '0.4043', '0.2515', '0.0863', '0.2428', '-0.04718', '0.3506', '-0.609', '0.464', '0.3596']",,,,,,,
mondo:0007344,"cluster headache, familial","['cluster headache, familial', 'hereditary cluster headache syndrome']",,119915,,C1861513,,,,C566117,,,,
mondo:0007345,aorta coarctation,"['coarctation of the aorta', 'aortic coarctation', 'coarctation of aorta']",,120000,1457,C0003492,,C84567,1001267,D001017,747.10,Q25.1,10009807,
mondo:0007346,cochleosaccular degeneration-cataract syndrome,"['COCHLEOSACCULAR degeneration with progressive cataracts', 'Cochleosaccular Degeneration of the inner Ear with progressive cataracts', 'Cochleosaccular degeneration of the inner ear and progressive cataracts', 'Cochleosaccular Degeneration']",,120040,3233,C1861512,,,,C536432,,,,
mondo:0007349,familial cold autoinflammatory syndrome 1,"['cold-induced autoinflammatory syndrome, familial', 'Fcas', 'cold hypersensitivity', 'familial cold autoinflammatory syndrome caused by mutation in NLRP3', 'familial cold inflammatory syndrome 1', 'familial cold autoinflammatory syndrome type 1', 'familial cold autoinflammatory syndrome 1', 'Cryopyrin-associated periodic syndrome 1', 'cold urticaria, familial', 'NLRP3 familial cold autoinflammatory syndrome', 'FCAS1']",0090062,120100,,,,,,,,,,
mondo:0007350,"coloboma, ocular, autosomal dominant","['coloboma of iris, choroid, and retina', 'coloboma, Uveoretinal', 'coloboma, ocular, autosomal dominant', 'coloboma, ocular']",,120200,,,"['-0.06537', '0.0711', '0.03204', '-0.05096', '0.0569', '-0.1255', '0.03293', '0.09845', '-0.0985', '-0.0671', '-0.0532', '-0.0556', '-0.01901', '0.01869', '-0.0561', '-0.04266', '0.02795', '-0.0837', '0.00399', '-0.1818', '-0.0459', '-0.0201', '0.03943', '-0.003645', '0.0442', '-0.002821', '-0.06793', '-0.01901', '0.04935', '-0.06036', '0.0884', '-0.01116', '0.1019', '0.0472', '0.002493', '-0.02739', '0.0003211', '-0.0709', '-0.009705', '-0.1177', '0.06052', '-0.1025', '0.03041', '-0.02255', '-0.015564', '-0.1305', '-0.0338', '0.0789', '0.0318', '0.01703', '-0.007236', '0.02261', '0.00954', '-0.04712', '-0.02975', '-0.0931', '0.1188', '-0.00707', '-0.1466', '-0.0205', '0.06003', '0.014', '0.004597', '0.02228', '-0.01334', '-0.01006', '0.12006', '0.1074', '-0.0767', '0.11127', '-0.08484', '0.02345', '0.04315', '-0.0706', '0.05795', '0.02101', '0.03912', '-0.04013', '-0.05743', '-0.05597', '-0.00538', '0.014206', '0.01183', '0.1517', '-0.011566', '0.01944', '0.0349', '0.1231', '0.0626', '0.071', '0.007248', '0.1202', '0.02478', '0.01726', '0.2505', '0.02481', '0.1208', '-0.1175', '-0.010574', '0.077']",,,,,,,
mondo:0007351,coloboma of macula,"['hereditary macular coloboma (subtype)', 'macular coloboma', 'agenesis of macula', 'coloboma of macula']",,120300,98945,,,,,,,,,
mondo:0007352,renal coloboma syndrome,"['optic coloboma, vesicoureteral reflux, and renal anomalies', 'congenital anomalies of the kidney and urinary tract with or without ocular abnormalities', 'optic coloboma, vesicoureteral reflux and renal anomalies', 'renal-coloboma syndrome with macular abnormalities', 'papillo-renal syndrome, optic nerve coloboma with renal disease', 'CAKUT with or without ocular abnormalities', 'Papillo-renal syndrome', 'renal-coloboma syndrome', 'coloboma of optic nerve with renal disease', 'PAPRS', 'optic nerve coloboma with renal disease', 'papillorenal syndrome', 'PAPILLORENAL syndrome']",0090006,120330,1475,C1852759,"['0.1428', '-0.3596', '0.03702', '0.303', '-0.2028', '0.09937', '-0.2852', '0.9365', '-0.3105', '-0.4365', '0.05728', '-0.716', '-0.4133', '0.518', '-0.3262', '-0.06836', '0.4097', '-0.2429', '0.5376', '-0.412', '0.1654', '-0.2198', '0.638', '0.3071', '0.2141', '0.2568', '-0.57', '0.4856', '0.3267', '0.4924', '0.5312', '-0.468', '0.6772', '0.0855', '0.03546', '-0.1169', '0.10266', '-0.4019', '0.3718', '-0.3115', '-0.4756', '-0.1473', '0.582', '-0.4832', '-0.006092', '-0.688', '-0.1362', '0.1282', '-0.0611', '-0.1693', '0.2537', '0.321', '0.0317', '-0.6387', '0.0385', '-0.03662', '0.04126', '-0.2795', '-0.4258', '0.2374', '0.218', '-0.1779', '0.2944', '0.0629', '0.01895', '-0.576', '0.541', '0.824', '-0.305', '0.5454', '-0.006313', '0.00815', '0.1209', '0.2798', '0.1282', '-0.613', '0.4592', '-0.0772', '-0.832', '-0.0558', '0.5913', '0.1508', '0.4624', '0.652', '-0.4019', '-0.32', '0.7026', '-0.1151', '-0.089', '0.3188', '0.08514', '0.3364', '-0.7905', '0.4595', '1.063', '-0.4397', '0.0873', '-0.1244', '-0.01174', '0.546']",C123230,,C537168,759.89,Q60.4,,
mondo:0007353,coloboma of macula-brachydactyly type B syndrome,"['coloboma of macula with type B brachydactyly', 'Sorsby syndrome', 'apical dystrophy']",,120400,1471,C1852752,,,,C535969,,,,
mondo:0007354,coloboma of optic nerve,"['coloboma of optic disc', 'coloboma of optic nerve (disease)', 'optic nerve coloboma', 'optic nerve head pits, bilateral congenital', 'coloboma of optic papilla', 'morning glory Disc anomaly', 'congenital coloboma of the optic nerve']",11975,120430,98947,,"['-0.06616', '0.09576', '0.04916', '-0.002914', '0.014046', '-0.07043', '0.00943', '0.10516', '-0.09705', '-0.0416', '-0.02788', '-0.06274', '-0.01765', '-0.002113', '-0.06604', '-0.1114', '0.00573', '-0.04715', '-0.003792', '-0.1976', '0.00928', '-0.069', '0.03262', '0.01883', '0.03445', '-0.01735', '-0.05533', '0.04248', '0.03574', '-0.03497', '0.07733', '0.01473', '0.15', '0.0534', '0.03041', '-0.04547', '0.00598', '-0.0714', '-0.006683', '-0.1208', '0.0407', '-0.0917', '0.04614', '-0.0376', '0.002207', '-0.0684', '-0.006348', '0.0781', '0.00921', '0.03357', '-0.01279', '0.03906', '-0.007183', '-0.02545', '-0.03818', '-0.0344', '0.1511', '-0.0255', '-0.1567', '-0.003424', '0.03406', '0.01207', '0.00734', '0.07196', '-0.05', '0.02434', '0.11774', '0.1287', '-0.03308', '0.1306', '-0.04422', '0.04565', '0.07385', '-0.06836', '0.0473', '0.01974', '0.0358', '0.0088', '-0.08813', '-0.0819', '0.03232', '-0.04614', '-0.00606', '0.1566', '-0.05063', '-0.03168', '0.05542', '0.1156', '0.11', '0.0263', '0.0333', '0.1029', '0.01978', '0.052', '0.2437', '-0.01811', '0.1153', '-0.094', '-0.02165', '0.0673']",,,C535970,377.23,,,0000588
mondo:0007355,uveal coloboma-cleft lip and palate-intellectual disability,"['COB1', 'coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or intellectual disability', 'coloboma-microphthalmos syndrome', 'coloboma, ocular, with or without hearing impairment, cleft lip/palate, and/or mental retardation', 'uveal coloboma-cleft lip/palate-intellectual disability syndrome', 'uveal coloboma-cleft lip/palate-mental retardation syndrome', 'coloboma, cleft lip/palate and intellectual disability syndrome', 'coloboma, cleft lip/palate and mental retardation syndrome', 'coloboma-microphthalmos syndrome associated with sensorineural hearing loss, hematuria, and cleft lip/palate']",0111249,120433,1473,C0795902,"['-0.2708', '-0.003061', '0.1144', '0.02502', '0.0728', '-0.0879', '0.5044', '0.1555', '-0.338', '-0.4338', '-0.1954', '-0.3704', '-0.058', '-0.1758', '-0.1251', '0.0376', '0.1261', '-0.1959', '0.0752', '-0.449', '0.04343', '0.1989', '0.1708', '-0.004143', '0.3035', '0.0964', '-0.479', '0.11945', '0.3794', '-0.0115', '0.368', '-0.1669', '0.173', '0.3484', '0.222', '-0.324', '-0.0663', '-0.574', '-0.3137', '-0.3525', '0.431', '-0.3457', '0.2413', '-0.2362', '-0.1724', '-0.1846', '0.0442', '-0.0379', '-0.2366', '0.1757', '-0.34', '0.04883', '-0.03702', '-0.1957', '-0.0151', '-0.5723', '0.6206', '-0.1803', '-0.2625', '0.00817', '0.1511', '-0.4368', '-0.02167', '0.1273', '-0.685', '-0.3694', '0.3206', '0.7036', '-0.1265', '-0.04813', '-0.363', '0.1432', '0.1517', '-0.1423', '0.0876', '-0.1567', '0.11816', '-0.3188', '-0.2368', '0.0258', '0.2426', '0.0499', '0.2556', '0.9355', '-0.0802', '-0.0901', '-0.05267', '0.5796', '-0.06036', '0.4155', '0.1782', '0.7246', '0.3625', '0.0417', '1.082', '-0.422', '0.358', '-0.348', '0.3245', '0.16']",,,C535971,,,,
mondo:0007356,Lynch syndrome 1,"['Lynch syndrome 2', 'HNPCC1', 'colon cancer, familial nonpolyposis, type 1', 'colorectal cancer, hereditary nonpolyposis, type 1', 'Lynch syndrome type 1', 'COCA1', 'LYNCH syndrome I', 'hereditary nonpolyposis colorectal cancer type 1', 'familial non-polyposis colon cancer type 1', 'Lynch 1 syndrome', 'Hereditary non-polyposis colon cancer type 1']",0070271,120435,,,,C6725,,C537261,,,,
mondo:0007357,colonic varices without portal hypertension,['colonic varices without portal hypertension'],,120440,,C1852721,,,,C565172,,,,
mondo:0007358,"comedones, familial Dyskeratotic","['comedones, familial Dyskeratotic']",,120450,,C0345424,,,,C562838,757.39,,,
mondo:0007359,commissural lip pits,['commissural lip pits'],,120500,,,,,,,,,,
mondo:0007360,branchiootic syndrome 2,"['bo syndrome 2', 'branchiootic syndrome type 2', 'branchiootic syndrome 2']",,120502,,C1852718,,,,C565171,,,,
mondo:0007361,C1 inhibitor deficiency,"['Quincke oedema', 'complement component 4, partial deficiency OF']",0060002,120790,459353,C1852700,"['-0.1274', '0.087', '-0.416', '-0.1403', '0.1179', '-0.2152', '0.1846', '-0.612', '-0.2063', '0.0505', '-0.1219', '0.1981', '-0.03032', '0.02263', '-0.002878', '-0.00983', '-0.3425', '-0.04153', '-0.506', '-0.4695', '0.2854', '-0.3105', '0.858', '-0.1256', '0.05554', '0.1466', '-0.1442', '0.1532', '-0.010376', '-0.1842', '0.2087', '0.2318', '0.525', '-0.08014', '0.232', '-0.11865', '-0.3286', '0.1076', '-0.11865', '-0.38', '-0.1543', '0.1873', '0.1984', '-0.196', '-0.03084', '-0.5786', '0.2476', '-0.2256', '0.2307', '0.4268', '-0.2773', '-0.02003', '0.305', '-0.1587', '-0.5938', '0.013275', '0.1648', '-0.3567', '-0.4304', '0.00265', '-0.0655', '0.1008', '-0.067', '0.3438', '0.402', '0.3796', '0.252', '0.3198', '-0.2465', '0.393', '-0.2131', '-0.1545', '-0.01904', '-0.1694', '0.1708', '-0.03516', '0.4062', '0.2798', '0.2423', '-0.1544', '-0.1913', '-0.306', '-0.1272', '0.2224', '-0.092', '-0.2113', '0.396', '0.1873', '0.1754', '-0.00401', '0.2612', '-0.0919', '-0.02348', '-0.259', '0.7417', '0.7637', '0.3591', '-0.2189', '-0.3047', '-0.1112']",,,,,,,
mondo:0007362,cone-rod dystrophy 2,"['cone-rod dystrophy', 'CORD2', 'CRD2', 'CRX cone-rod dystrophy', 'retinal cone-rod dystrophy 2', 'cone-rod dystrophy 2', 'cone-rod retinal dystrophy 2', 'cone-rod dystrophy caused by mutation in CRX', 'retinal cone-rod dystrophy', 'cone-rod retinal dystrophy', 'cone-rod dystrophy type 2', 'RCRD2', 'cone-rod retinal dystrophy-2']",0111005,120970,,CN074280,,C162399,,,362.75,,,
mondo:0007363,congenital contractural arachnodactyly,"['distal arthrogryposis type 9', 'Beals-Hecht syndrome', 'contractures, multiple with arachnodactyly', 'Beals syndrome', 'arachnodactyly, contractural Beals type', 'contractural arachnodactyly, congenital', 'DA9', 'CCA', 'CCA syndrome', 'arthrogryposis, distal, type 9', 'Ear anomalies-contractures-dysplasia of bone with kyphoscoliosis']",0111595,121050,115,C0220668,"['-0.0192', '0.04193', '0.312', '-0.1973', '0.399', '-0.702', '0.3384', '0.678', '-0.6865', '-0.2805', '0.1904', '-0.1808', '0.013', '-0.2065', '0.054', '0.1644', '0.01182', '-0.0998', '-0.5684', '-0.4587', '-0.02989', '-0.1772', '0.1678', '0.1611', '0.1464', '0.2688', '-0.1769', '0.1207', '0.3213', '-0.165', '0.2408', '0.1736', '0.1084', '0.1064', '-0.1092', '-0.3523', '0.31', '-0.2812', '0.2172', '-0.3916', '0.0754', '-0.263', '-0.00799', '0.3167', '0.10425', '-0.2083', '0.264', '0.336', '0.19', '-0.2249', '-0.2136', '-0.2358', '0.2476', '0.01738', '-0.2498', '-0.27', '0.3162', '0.2249', '-0.1427', '0.1247', '0.527', '0.1736', '-0.2065', '0.0463', '0.3425', '-0.0908', '-0.0696', '0.12256', '-0.1393', '-0.03497', '-0.5034', '-0.1084', '-0.002113', '-0.0628', '0.2717', '-0.00256', '-0.00624', '-0.12354', '-0.619', '-0.3267', '0.2825', '-0.303', '-0.2069', '0.5996', '-0.4343', '0.2363', '-0.129', '0.11414', '-0.1154', '-0.00451', '0.1713', '0.1871', '-0.1453', '-0.000994', '0.2507', '0.08405', '0.873', '-0.4087', '0.1892', '0.0765']",C129865,,C536211,759.89,,,
mondo:0007364,"arthrogryposis, distal, type 2E","['arthrogryposis, distal, type 2E', 'contractures of fingers and jaw']",,121070,,C1852597,,,,C535384,,,,
mondo:0007365,"seizures, benign familial neonatal, 1","['KCNQ2 benign neonatal seizures', 'myokymia', 'benign neonatal seizures caused by mutation in KCNQ2', 'seizures, benign familial neonatal, 1, and/or myokymia', 'seizures, benign familial neonatal, type 1', 'epilepsy, benign neonatal, 1, and/or myokymia', 'BFNS1', 'seizures, benign familial neonatal, 1', 'seizures, benign neonatal, 1']",,121200,,C3149074,,,,C567743,,,,
mondo:0007366,"seizures, benign familial neonatal, 2","['KCNQ3 benign neonatal seizures', 'BFNS2', 'seizures, benign familial neonatal, 2', 'convulsions, benign familial neonatal, 2', 'seizures, benign familial neonatal, type 2', 'benign neonatal seizures caused by mutation in KCNQ3', 'seizures, benign neonatal, 2']",,121201,,C1852581,,,,,,,,
mondo:0007367,"febrile seizures, familial, 1","['febrile seizures, familial, 1', 'convulsions, familial febrile, 1', 'FEB1', 'convulsions, familial febrile']",0111307,121210,,C1852577,,,,C565162,780.39,,,
mondo:0007368,familial benign copper deficiency,"['familial benign hypocupremia', 'copper deficiency, familial benign']",,121270,1551,C1852576,,,,C535468,,,,
mondo:0007369,hereditary coproporphyria,"['HCP', 'Cpx deficiency', 'Harderoporphyria', 'hereditary coproporphyria', 'hereditary coproporphyria porphyria', 'porphyria hepatica coproporphyria', 'coproporphyria', 'Cpo deficiency', 'Cpox deficiency', 'coproporphyria hereditary', 'coproporphyria, hereditary', 'porphyria hepatica II', 'coproporphyrinogen oxidase deficiency', 'CPRO deficiency']",13269,121300,79273,C0162531,"['0.10315', '-0.10236', '-0.6523', '-0.69', '-0.1287', '-0.3408', '0.2174', '-0.1798', '-0.4473', '0.02045', '-0.3308', '0.5356', '-0.01857', '1.354', '-0.8433', '0.07904', '0.179', '0.3433', '-0.5146', '-0.5933', '-0.3027', '-0.2698', '0.225', '-0.3455', '0.04166', '-0.579', '-0.08167', '0.01659', '0.4683', '-0.588', '-0.05328', '-0.586', '0.801', '-1.029', '-0.2874', '-0.5317', '-0.61', '-0.1475', '-0.03537', '-0.126', '0.5273', '-0.416', '0.1821', '-0.36', '-0.010345', '-0.4263', '0.2622', '-0.3013', '0.877', '0.374', '-0.2279', '0.56', '1.011', '0.1294', '-0.001791', '-0.2507', '0.0551', '-0.02644', '-0.04727', '-0.2336', '-0.04514', '-0.2537', '0.925', '-0.05063', '-0.239', '0.5806', '0.0438', '0.8745', '0.2751', '0.1311', '-0.3542', '-0.1534', '0.311', '-0.9453', '0.1295', '0.545', '0.4255', '-0.11536', '0.0469', '-0.552', '0.5586', '-0.795', '0.2795', '-0.4421', '0.473', '0.2001', '1.184', '0.4146', '-0.2246', '-0.006176', '0.7354', '-0.2427', '-0.4094', '0.4038', '0.1694', '0.9014', '0.232', '-0.5283', '0.3118', '0.3535']",C84759,,D046349,,,10019866,
mondo:0007370,"coracoclavicular joint, anomalous","['coracoclavicular joint, anomalous']",,121350,,,,,,C565161,,,,
mondo:0007371,cornea guttata with anterior polar cataracts,"['cornea guttata with anterior polar cataract', 'familial congenital cornea guttata with anterior polar cataracts (type)', 'cornea guttata with anterior polar cataracts']",,121390,,C1852558,,,,C535471,,,,
mondo:0007372,"cornea plana 1, autosomal dominant","['CNA1', 'cornea plana 1', 'cornea plana 1, autosomal dominant']",,121400,,C1852557,,,,C565158,,,,
mondo:0007373,"corneal degeneration, ribbonlike, with deafness","['band keratopathy with deafness', 'corneal degeneration, ribbonlike, with deafness']",,121450,,C1852556,,,,C565157,,,,
mondo:0007374,Schnyder corneal dystrophy,"['hereditary crystalline stromal dystrophy of Schnyder', 'corneal dystrophy, Schnyder', 'Schnyder crystalline dystrophy sine crystals', 'Schnyder corneal dystrophy', 'corneal dystrophy, Schnyder type', 'SCCD', 'SCD', 'corneal dystrophy, crystalline, of Schnyder', 'Schnyder crystalline corneal dystrophy', 'crystalline stromal dystrophy', 'corneal dystrophy crystalline of Schnyder']",0060456,121800,98967,,"['-0.705', '-0.03165', '-0.4807', '0.1724', '0.6953', '-0.575', '-0.2708', '0.05002', '-0.2905', '-0.588', '-0.2048', '-0.39', '-0.2947', '0.2888', '-0.2417', '-0.6904', '0.534', '-0.278', '-0.0889', '-0.7197', '-0.2227', '0.04413', '0.1456', '-0.1616', '-0.4424', '0.506', '-0.6753', '-0.097', '-0.4985', '0.2028', '0.8794', '-0.01787', '0.1631', '0.0507', '0.1277', '0.02641', '-0.3623', '-0.547', '0.0178', '-0.3296', '0.7153', '-0.2351', '0.04895', '-0.0653', '-0.1072', '0.731', '0.02046', '-0.2465', '0.1139', '0.3638', '0.6855', '0.6953', '0.7534', '0.2045', '-0.2725', '-0.1912', '0.1478', '0.3718', '-0.894', '0.09467', '0.5957', '-0.4001', '0.2406', '-0.1417', '-0.276', '-0.487', '0.5493', '1.1875', '-0.0972', '0.7896', '0.11743', '-0.2035', '0.0449', '0.1288', '0.6396', '0.0799', '-0.12463', '0.055', '-0.2258', '-0.08496', '-0.11', '-0.4578', '-0.11127', '0.558', '-0.04263', '-0.3794', '-0.4263', '0.11884', '0.1853', '-0.11194', '-0.2435', '0.2001', '-0.313', '0.336', '0.1692', '0.03592', '0.4424', '-0.4307', '-0.163', '0.1263']",,,C535475,,,,
mondo:0007375,epithelial basement membrane dystrophy,"['EBMD', 'corneal dystrophy, Map-Dot-Fingerprint type', 'corneal dystrophy, anterior basement Membrane', 'anterior basement membrane dystrophy', 'Map-dot-fingerprint dystrophy of cornea', 'corneal dystrophy, microcystic', 'Cogan corneal dystrophy', 'Map-dot-fingerprint dystrophy', 'Cogan microcystic epithelial dystrophy', 'microcystic corneal dystrophy', 'corneal dystrophy, epithelial basement MEMBRANE', 'microcystic dystrophy of the cornea', 'epithelial basement membrane corneal dystrophy']",0060447,121820,98956,,"['-0.0412', '0.0693', '-0.134', '0.0087', '0.1345', '-0.4038', '-0.4336', '0.04373', '-0.1175', '-0.5083', '-0.1648', '0.1206', '-0.004868', '0.03293', '-0.0347', '-0.05994', '0.2783', '-0.2015', '0.3003', '-0.7617', '-0.258', '0.1174', '0.3574', '0.4556', '0.02725', '0.0096', '-0.0414', '0.1958', '-0.2617', '0.07495', '0.5376', '0.02237', '-0.12354', '0.2966', '0.04855', '0.5576', '0.02559', '0.05737', '0.2136', '-0.3335', '0.3782', '-0.1995', '0.1434', '0.4478', '-0.0973', '-0.1644', '-0.4536', '0.1843', '0.08765', '0.1699', '0.5107', '0.0941', '0.03035', '-0.161', '0.1791', '-0.1214', '0.659', '0.2086', '-0.3577', '-0.11', '0.2336', '-0.0498', '-0.1324', '0.1214', '0.2295', '-0.264', '0.9062', '0.6953', '-0.0308', '0.557', '-0.1718', '-0.2136', '0.306', '0.12225', '0.3713', '-0.1859', '0.2225', '0.1556', '0.1509', '-0.3252', '-0.2155', '-0.08203', '0.291', '0.2856', '-0.11316', '-0.07904', '-0.3308', '0.0989', '-0.05695', '0.2673', '0.3044', '0.4036', '0.1021', '0.381', '0.3816', '0.157', '0.271', '-0.5396', '-0.1509', '0.1426']",,,C535477,,,,
mondo:0007376,fleck corneal dystrophy,"['Cfd', 'Francois-Neetens speckled corneal dystrophy', 'FranC^ois-Neetens speckled corneal dystrophy', 'corneal dystrophy, Francois-Neetens speckled or flecked', 'fleck corneal dystrophy', 'François-Neetens speckled corneal dystrophy', 'FCD', 'corneal dystrophy, FLECK', 'corneal fleck dystrophy']",0060448,121850,98970,C1562113,"['-0.4675', '-0.2106', '-0.5645', '0.1725', '0.7417', '-0.9365', '-0.3638', '0.4717', '-0.2292', '-0.503', '0.2051', '-0.322', '0.1329', '0.613', '-0.003866', '-0.1203', '0.1248', '-0.474', '0.00852', '-0.9883', '-0.627', '-0.0519', '0.2554', '0.5483', '-0.2458', '0.1588', '-0.7856', '-0.392', '-0.5093', '0.4768', '0.7505', '0.1506', '0.3215', '-0.058', '0.1674', '-0.1354', '-0.3552', '-0.4617', '0.2126', '-0.2117', '0.6265', '-0.3215', '0.0867', '-0.01456', '0.1415', '0.57', '0.1084', '0.06073', '0.05704', '0.4229', '0.6675', '0.2347', '0.7534', '-0.3857', '-0.0604', '0.2019', '0.409', '-0.1367', '-0.5264', '0.1221', '0.2395', '-0.4727', '0.3281', '-0.07275', '0.12195', '0.2074', '0.6265', '0.5044', '-0.329', '0.559', '0.106', '-0.6367', '0.1569', '0.02667', '0.721', '-0.11676', '0.1611', '0.3535', '-0.1755', '0.142', '-0.32', '-0.06158', '0.1718', '0.3506', '-0.1522', '-0.5986', '-0.518', '-0.3066', '0.3015', '0.411', '0.0696', '0.47', '0.3025', '-0.12494', '0.1324', '0.1417', '0.2793', '-0.957', '0.2311', '0.4272']",,,C563256,371.56,,,
mondo:0007377,granular corneal dystrophy type I,"['granular corneal dystrophy type 1', 'corneal dystrophy Groenouw type I', 'corneal dystrophy granular type', 'GCD1', 'corneal dystrophy, Groenouw type I', 'CDGG1', 'corneal dystrophy, punctate or nodular', 'GCDI', 'classic granular corneal dystrophy', 'corneal dystrophy punctate or nodular', 'granular corneal dystrophy, type 1', 'Groenouw type I corneal dystrophy', 'corneal dystrophy, Groenouw type 1', 'classic GCD']",0080530,121900,98962,C1641846,"['-0.05087', '-0.03287', '-0.5176', '-0.1266', '0.233', '-0.4573', '-0.187', '0.01123', '-0.584', '-0.709', '-0.0408', '0.1586', '-0.3342', '0.6113', '-0.03366', '-0.4934', '0.35', '-0.51', '0.2142', '-0.6426', '-0.5337', '0.11975', '0.432', '0.4187', '-0.2654', '0.461', '-0.0606', '0.10126', '-0.525', '0.466', '0.643', '0.208', '0.1792', '0.275', '0.1506', '0.451', '-0.1954', '-0.00841', '0.05103', '0.09216', '0.311', '-0.2612', '0.2598', '0.3767', '0.03568', '0.09576', '-0.197', '-0.02307', '0.178', '0.03745', '0.9873', '0.12476', '0.273', '-0.9536', '-0.1119', '0.10803', '0.603', '-0.03574', '-0.6997', '0.2445', '0.01059', '-0.2996', '0.04965', '0.2854', '0.1498', '-0.3706', '1.193', '1.042', '0.09955', '0.5933', '0.12146', '-0.2654', '0.4426', '0.128', '0.7065', '0.2888', '-0.08673', '0.436', '-0.2238', '0.03958', '0.001598', '-0.2405', '-0.3115', '0.375', '-0.1039', '-0.10376', '0.05258', '0.01329', '0.1414', '0.4346', '0.2133', '0.549', '0.2852', '0.357', '0.1713', '0.1964', '0.4788', '-0.6436', '-0.06415', '0.0992']",,,C537304,,,,
mondo:0007378,posterior polymorphous corneal dystrophy 1,"['corneal dystrophy, POSTERIOR polymorphous, 1', 'corneal endothelial dystrophy 1, autosomal dominant, formerly', 'Ppcd1', 'Maumenee corneal dystrophy', 'posterior polymorphous corneal dystrophy', 'corneal dystrophy, hereditary polymorphous posterior', 'Ched1', 'corneal dystrophy, posterior polymorphous, type 1', 'corneal endothelial dystrophy 1, autosomal dominant', 'PPCD1', 'posterior polymorphous corneal dystrophy type 1']",0110855,122000,,CN029625,,,,,371.58,,,
mondo:0007379,Meesmann corneal dystrophy,"['corneal dystrophy, juvenile epithelial, of Meesmann', 'MECD', 'juvenile epithelial of Meesmann corneal dystrophy', 'juvenile hereditary epithelial dystrophy of Meesmann', 'corneal dystrophy, Meesmann', 'Meesmann corneal epithelial dystrophy', 'Meesman dystrophy', 'stocker-Holt dystrophy', 'juvenile hereditary epithelial dystrophy', 'corneal dystrophy, Meesmann epithelial', 'Meesmann corneal dystrophy', 'corneal dystrophy, juvenile epithelial of Meesmann']",0060451,,98954,C0339277,"['-0.3313', '-0.2086', '-0.629', '0.02731', '0.01596', '-0.5264', '-0.4648', '0.6147', '0.3142', '-0.2366', '-0.1437', '-0.2317', '-0.3965', '0.4302', '-0.1647', '0.3186', '0.2832', '-0.548', '0.4575', '-0.606', '-0.7886', '0.222', '0.2041', '0.1724', '-0.6562', '0.2644', '-0.3733', '-0.00876', '-0.4595', '0.0653', '0.535', '0.1676', '-0.09033', '-0.0498', '-0.148', '0.05014', '0.1562', '-0.292', '0.64', '-0.442', '0.261', '-0.2998', '-0.1126', '0.1235', '-0.1854', '0.3066', '0.06903', '-0.3044', '0.3257', '-0.02898', '0.4802', '0.04117', '0.431', '0.0519', '-0.263', '0.3174', '0.4766', '0.1108', '-0.2328', '0.2369', '0.11395', '-0.2976', '-0.07837', '0.4353', '-0.1898', '-0.29', '0.808', '1.031', '-0.06616', '0.6675', '-0.3552', '-0.441', '0.1711', '0.5474', '0.3704', '0.453', '0.0538', '0.3735', '-0.03024', '0.3926', '-0.2205', '-0.1406', '-0.5293', '0.1996', '-0.1565', '-0.419', '0.1694', '0.08954', '0.2045', '0.2323', '0.262', '0.54', '0.4084', '0.2063', '0.857', '-0.2275', '0.2152', '-1.019', '0.07874', '0.1074']",C84795,,D053559,371.51,,,
mondo:0007380,lattice corneal dystrophy type I,"['Biber-Haab-Dimmer dystrophy', 'classic lattice corneal dystrophy', 'corneal dystrophy, lattice type I', 'lattice corneal dystrophy type 1', 'LCDI', 'lattice corneal dystrophy, type 1', 'corneal dystrophy, lattice type 1', 'Lcd1', 'LCD', 'CDL1']",,122200,98964,CN207224,"['-0.322', '-0.0682', '-0.7964', '0.2793', '-0.03992', '-0.569', '-0.313', '0.4', '-0.1343', '-0.494', '-0.3015', '-0.2485', '-0.4824', '0.108', '0.013145', '-0.416', '0.2152', '-0.8555', '0.2157', '-0.774', '-0.4849', '-0.03091', '0.4387', '0.2029', '0.0698', '0.3748', '-0.4946', '0.2056', '-0.717', '0.1768', '0.5938', '0.146', '-0.1995', '0.237', '0.1875', '-0.0522', '0.1604', '-0.09955', '0.2651', '0.2083', '0.1177', '-0.03543', '0.572', '0.3787', '0.09485', '0.3848', '-0.11896', '-0.1317', '0.1388', '0.282', '0.997', '0.02611', '0.02702', '-0.5474', '0.2277', '0.08466', '0.6396', '-0.3342', '-0.621', '0.06976', '0.2411', '-0.497', '0.1311', '0.09265', '0.0413', '-0.488', '1.009', '0.715', '-0.399', '0.6167', '-0.05167', '-0.3164', '0.533', '-0.2583', '0.828', '0.0313', '-0.2744', '0.7007', '-0.5063', '-0.1803', '-0.4602', '-0.379', '-0.2324', '0.4111', '-0.0752', '0.0913', '0.0659', '-0.001322', '0.2076', '-0.2456', '0.1757', '0.553', '0.1166', '-0.0848', '0.3533', '-0.02077', '0.3772', '-0.7593', '-0.02599', '0.392']",,,C537881,,,,
mondo:0007381,epithelial recurrent erosion dystrophy,"['dystrophia Helsinglandica', 'dystrophia Smolandiensis', 'recurrent hereditary corneal erosions', 'epithelial recurrent erosion dystrophy', 'corneal erosions, recurring hereditary', 'ERED']",0070337,122400,293381,C1852551,"['-0.01209', '-0.2905', '-0.951', '-0.3665', '-0.0806', '-0.1765', '0.4746', '0.12024', '0.415', '-0.693', '-0.1917', '0.3657', '-0.6865', '0.1335', '-0.1615', '-0.1089', '0.632', '-0.03867', '0.2717', '-0.931', '-0.3992', '-0.003792', '0.1836', '-0.2617', '-0.657', '0.4895', '-0.244', '0.0487', '-0.3213', '0.2074', '0.4436', '0.1432', '0.47', '0.261', '-0.03485', '0.4048', '-0.03427', '-0.406', '0.03812', '0.2261', '0.806', '-0.6133', '0.3923', '0.524', '0.01883', '0.242', '-0.7456', '-0.182', '0.11035', '0.857', '-0.2876', '0.002201', '0.1443', '-0.4038', '-0.045', '-0.06256', '0.6777', '0.3577', '-0.2388', '-0.8633', '-0.2208', '0.03894', '0.01542', '0.4854', '0.2423', '0.1236', '0.814', '1.174', '-0.01562', '0.3953', '-0.1464', '-0.1244', '0.2433', '-0.2264', '1.106', '0.3584', '0.1092', '0.1715', '-0.2161', '0.02145', '-0.0756', '0.04053', '0.1787', '0.2683', '-0.05194', '-0.114', '-0.3252', '0.8022', '0.338', '0.1061', '0.582', '0.8438', '0.0495', '0.4429', '0.3074', '-0.2756', '-0.3735', '-0.718', '-0.377', '-0.3518']",,,C565155,,,,
mondo:0007382,Ramos-Arroyo syndrome,"['congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and intellectual disability', 'corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and intellectual disability', 'corneal anesthesia-deafness-intellectual disability syndrome', 'congenital corneal anaesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and intellectual disability', 'congenital corneal anaesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation', 'Ramos-Arroyo syndrome', 'Ramos Arroyo Clark syndrome', 'corneal hypesthesia with retinal abnormalities, sensorineural deafness, unusual facies, persistent ductus arteriosus, and mental retardation', 'congenital corneal anesthesia with retinal abnormalities, deafness, unusual facies, persistent ductus arteriosus, and mental retardation']",,122430,1051,C2930866,,,,C535286,,,,
mondo:0007383,Stern-Lubinsky-Durrie syndrome,"['corneal dystrophy epithelial and short stature', 'corneo-dermato-osseous syndrome', 'Cdo syndrome', 'Stern Lubinsky Durrie syndrome', 'corneal dystrophy, epithelial, with skin and skeletal changes', 'CORNEODERMATOOSSEOUS syndrome']",,122440,3194,,,,,C537488,,,,
mondo:0007384,congenital trigeminal anesthesia,"['familial trigeminal anaesthesia', 'trigeminal anesthesia, familial', 'corneal hypesthesia, familial', 'familial trigeminal anesthesia']",,122450,231013,C1852541,,,,C536440,,,,
mondo:0007385,idiopathic spontaneous coronary artery dissection,"['coronary artery dissection, spontaneous', 'idiopathic SCAD']",,122455,458718,C1852540,,,,C565153,,,,
mondo:0007387,Cornelia de Lange syndrome 1,"['Cornelia De Lange syndrome type 1', 'Cornelia de Lange syndrome 1', 'Cornelia DE Lange syndrome 1', 'NIPBL Cornelia de Lange syndrome', 'Cornelia de Lange syndrome caused by mutation in NIPBL', 'Brachmann-De Lange syndrome', 'Cdl', 'typus Degenerativus Amstelodamensis', 'De Lange syndrome', 'CDLS1']",0080505,122470,,CN029798,,,,,759.89,,,
mondo:0007388,congenitally short costocoracoid ligament,"['fixation of the scapula to the first rib by a congenitally short costocoracoid ligament', 'congenital shortness of the costocoracoid ligament', 'costocoracoid ligament, congenitally short', 'costocoracoid ligament congenitally short']",,122580,2391,,,,,C536448,,,,
mondo:0007389,spondylocostal dysostosis 5,"['costovertebral segmentation anomalies', 'TBX6 spondylocostal dysostosis', 'spondylocostal dysostosis 5', 'polydysspondyly', 'spondylocostal dysplasia', 'spondylothoracic dysostosis', 'spondylocostal dysostosis caused by mutation in TBX6', 'scoliosis, congenital, with or without rib anomalies', 'spondylocostal dysostosis type 5', 'SCDO5']",0112363,122600,1797,C4083048,,,,,,,,
mondo:0007390,coumarin resistance,"['coumarin resistance', 'warfarin resistance', 'coumarin sensitivity', 'coumarin, poor metabolism of', 'warfarin sensitivity']",0080665,122700,,CN078029,,,,C563039,,,,
mondo:0007391,coxa vara,"['coxa vara', 'coxa vara, congenital', 'coxa vara (disease)']",,122750,,,,,1001298,D060905,,,,0002812
mondo:0007392,coxoauricular syndrome,['coxoauricular syndrome'],,122780,1508,C1852513,,,,C565148,,,,
mondo:0007393,cranioacrofacial syndrome,['Cranioacrofacial syndrome'],,122850,1339,C1852512,,,,C565147,,,,
mondo:0007395,craniofacial-deafness-hand syndrome,"['Sommer-Young-Wee-Frye syndrome', 'features of flat facial profile, hypertelorism, hypoplastic nose with slitlike nares, and a sensorineural hearing loss', 'craniofacial-deafness-hand syndrome', 'craniofacial deafness hand syndrome', 'CDHS']",0111336,122880,1529,,"['-0.137', '0.2495', '0.3772', '-0.1133', '0.0693', '-0.2896', '-0.3015', '0.3403', '-0.4397', '-0.352', '0.0905', '-0.1572', '-0.03111', '-0.292', '-0.1367', '0.0693', '0.4983', '-0.1855', '0.004223', '-0.2189', '0.0828', '-0.06274', '0.3115', '0.11707', '0.4563', '0.272', '-0.4133', '-0.003403', '0.5654', '-0.52', '0.1478', '-0.1752', '0.1777', '0.1805', '-0.1571', '-0.09015', '-0.2417', '0.11395', '-0.1923', '-0.525', '0.2915', '-0.3599', '-0.1962', '-0.3242', '0.0931', '-0.4265', '-0.0375', '0.5635', '-0.3213', '-0.259', '-0.03873', '-0.3977', '-0.3464', '-0.01999', '-0.0835', '-0.7134', '0.0755', '-0.0782', '-0.395', '0.1388', '-0.02896', '-0.0638', '-0.2957', '0.1858', '0.08606', '-0.1923', '0.0983', '-0.05695', '-0.2477', '0.5674', '-0.507', '0.3025', '0.2837', '-0.0945', '-0.2078', '0.2125', '0.006813', '-0.05038', '-0.412', '-0.2203', '0.3247', '-0.04276', '0.11945', '0.8633', '-0.25', '0.148', '-0.3643', '0.4968', '0.0376', '0.1735', '0.05215', '0.656', '0.1342', '0.1984', '0.658', '-0.03008', '0.3613', '-0.6133', '0.2961', '0.04672']",,,C536453,759.89,,,
mondo:0007396,"dysostosis, Stanescu type","['autosomal dominant osteosclerosis, Stanescu type', 'craniofacial dysostosis-diaphyseal hyperplasia syndrome', 'craniofacial dysostosis with diaphyseal hyperplasia', 'Stanescu osteosclerosis', 'dysostosis Stanescu type', 'osteosclerosis, Stanescu type']",,122900,1798,C0432263,,,,C562974,,,,
mondo:0007397,"craniometaphyseal dysplasia, autosomal dominant","['craniometaphyseal dysplasia, autosomal dominant', 'craniometaphyseal dysplasia Jackson type', 'craniometaphyseal dysplasia, Jackson type', 'CMDD', 'CMD', 'CMDJ']",0080801,123000,,C1852502,,,,C565145,,,,
mondo:0007398,craniorhiny,['craniorhiny'],,123050,157832,C1852501,,,,C565144,,,,
mondo:0007399,TWIST1-related craniosynostosis,"['CRS1', 'craniostenosis', 'craniosynostosis 1', 'CRS', 'craniosynostosis type 1']",,123100,,CN029978,,,,,,,,
mondo:0007400,Jackson-Weiss syndrome,"['craniosynostosis, midfacial hypoplasia, and foot abnormalities', 'Jackson-Weiss syndrome', 'craniosynostosis-midfacial hypoplasia-foot abnormalities syndrome', 'JWS']",0111337,123150,1540,C0795998,"['-0.2263', '-0.05988', '0.0818', '-0.05676', '-0.00537', '-0.4114', '-0.2382', '0.5176', '-0.5244', '-0.4575', '-0.2339', '-0.1285', '0.1065', '0.2184', '0.02425', '0.007347', '0.3323', '-0.0893', '-0.1737', '-0.2396', '-0.0672', '0.264', '0.4895', '-0.2092', '0.3865', '0.1814', '-0.2123', '-0.02724', '0.375', '-0.2168', '0.2954', '-0.4424', '0.0552', '0.3022', '0.1075', '-0.276', '-0.13', '-0.2358', '-0.1761', '-0.2468', '-0.03032', '-0.2751', '-0.166', '-0.2017', '0.0634', '-0.2192', '0.083', '0.3494', '-0.241', '-0.2588', '-0.1666', '-0.1544', '-0.174', '0.1083', '-0.1918', '-0.31', '-0.10504', '-0.1948', '-0.04938', '0.3286', '0.1919', '-0.299', '-0.1709', '0.2468', '-0.2544', '0.003567', '-0.01926', '0.3135', '-0.491', '0.1898', '-0.4214', '0.0903', '0.033', '0.098', '-0.03244', '0.3118', '-0.0521', '-0.2668', '-0.2365', '-0.4553', '0.2015', '0.06744', '0.0382', '0.4717', '0.03708', '-0.05383', '-0.196', '0.1991', '0.2607', '-0.12054', '-0.2217', '0.4883', '0.0723', '0.1831', '0.545', '0.2615', '0.4417', '-0.4492', '0.4355', '-0.0532']",C123814,,C537559,759.89,,,
mondo:0007401,craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome,"['craniosynostosis-Dandy-Walker malformation-hydrocephalus syndrome', 'HDCPH1', 'hydrocephalus, autosomal dominant', 'Braddock-Jones-Superneau syndrome', 'sagittal craniosynostosis, Dandy-Walker malformation and hydrocephalus', 'Braddock Jones Superneau syndrome', 'Dandy-Walker malformation with sagittal craniosynostosis and hydrocephalus']",,123155,1538,CN199608,,,,C563973,,,,
mondo:0007402,"creatine phosphokinase, elevated serum","['CPK, elevated serum', 'hyperCKemia, idiopathic', 'creatine phosphokinase, elevated serum']",,123320,,,,,,,,,,
mondo:0007403,inherited Creutzfeldt-Jakob disease,"['CJD', 'Creutzfeldt-Jakob disease, variant', 'Creutzfeldt-Jakob disease, variant, resistance to', 'inherited CJD', 'Creutzfeldt-Jakob disease, sporadic', 'hereditary Creutzfeldt Jacob disease', 'Creutzfeldt-Jakob disease', 'Creutzfeldt-Jakob disease, Heidenhain variant', 'Creutzfeldt-Jakob disease, familial']",,123400,282166,CN202816,"['0.2362', '0.618', '-0.539', '0.5596', '-0.2495', '0.4458', '-0.383', '0.1239', '-0.1458', '0.0952', '-0.0803', '-0.10266', '-0.2517', '0.27', '0.3062', '-0.2993', '-0.549', '-0.4016', '-0.0995', '-0.7246', '-0.1718', '-0.2014', '-0.3025', '-0.9204', '0.2634', '-0.6353', '-0.437', '-0.1779', '-0.1047', '-0.1028', '0.849', '-0.6514', '0.004536', '-0.002268', '0.2725', '-0.08655', '-0.2861', '0.0976', '0.4597', '-0.2727', '0.1247', '-0.651', '0.1644', '-0.7617', '0.685', '-0.2164', '-0.5156', '-0.2175', '-0.2935', '0.3745', '-0.134', '-0.4011', '-0.069', '0.2734', '0.02998', '0.2435', '0.2532', '0.1797', '0.3298', '0.1147', '0.866', '0.3386', '-0.1807', '-0.1915', '-0.1228', '0.4768', '0.58', '-0.2441', '-0.935', '0.6304', '0.01397', '-0.001089', '-0.078', '-0.1534', '0.5347', '0.285', '0.02753', '0.4294', '-0.3672', '0.5396', '-0.26', '-0.818', '-0.545', '-0.1195', '-0.245', '-0.4573', '0.1326', '0.2654', '0.7417', '-0.1569', '0.1881', '-0.341', '-0.3088', '0.497', '0.1473', '0.181', '-0.3582', '-0.287', '0.3557', '-0.4573']",,,,,,,
mondo:0007404,Cri-du-chat syndrome,"['Cat Cry syndrome', 'chromosome 5p deletion syndrome', 'chromosome 5P deletion syndrome', 'chromosome 5p- syndrome', 'monosomy type 5p', 'Cat-Cry syndrome', 'Cri du chat syndrome', 'monosomy 5p', 'Cri-du-chat syndrome', 'deletion 5p', '5p minus syndrome', '5p- syndrome', 'chromosome 5 short arm deletion syndrome', '5p deletion syndrome', '5p partial monosomy syndrome']",12580,123450,281,CN776901,,C34518,,D003410,758.39,,10011385,
mondo:0007405,Crouzon syndrome,"['craniofacial dysostosis', 'Cfd1', 'Crouzon syndrome', 'Crouzon craniofacial dysostosis', 'Crouzon disease', 'craniofacial dysostosis type 1', 'craniofacial dysostosis, type 1', 'Crouzon^s disease']",2339,123500,207,CN200892,"['0.1555', '0.0416', '-0.1508', '0.01648', '0.4995', '-0.05878', '-0.03522', '0.6567', '-1.054', '-0.2993', '-0.1815', '-0.386', '-0.3193', '0.2046', '-0.2285', '-0.227', '0.034', '-0.4421', '-0.00958', '-0.623', '-0.3835', '-0.01062', '0.747', '-0.3374', '0.2717', '0.03964', '0.2258', '0.05286', '0.7485', '0.0989', '0.5156', '-0.05768', '0.05475', '0.1206', '-0.1259', '0.297', '0.289', '-0.1466', '-0.2167', '-0.04752', '0.264', '0.222', '0.2407', '-0.4849', '0.1164', '0.1832', '-0.4456', '0.09326', '-0.1941', '0.09015', '0.1305', '-0.5605', '0.1885', '-0.3472', '-0.004997', '0.0566', '0.04407', '0.385', '-0.177', '0.2255', '-0.10614', '-0.1451', '-0.1473', '-0.05188', '-0.3691', '-0.4265', '0.1489', '0.3716', '-0.1799', '0.4773', '-0.1664', '0.386', '0.2737', '-0.093', '-0.5127', '0.1924', '0.3477', '-0.7905', '-0.528', '-0.3818', '-0.10315', '-0.1101', '0.014275', '0.875', '-0.1459', '0.2556', '0.1898', '0.07', '0.345', '-0.0662', '-0.2622', '0.1709', '-0.1014', '-0.0423', '0.5044', '-0.193', '0.5312', '0.09406', '0.134', '0.0572']",C84653,,D003394,,,,
mondo:0007406,"cryofibrinogenemia, familial primary","['cryofibrinogenemia, familial primary']",,123540,,C1852457,,,,C565142,,,,
mondo:0007407,Cryoglobulinemic vasculitis,"['cryoglobulinemia, familial mixed', 'essential cryoglobulinemia', 'familial mixed cryoglobulinemia', 'essential mixed cryoglobulinemia', 'Meltzer syndrome', 'primary cryoglobulinemia', 'MC', 'mixed cryoglobulinemia']",,123550,91138,C1852456,,,,C565141,273.2,D89.1,10027756,
mondo:0007408,"cryptotia, familial","['cryptotia, familial']",,123557,,C1852455,,,,C565140,,,,
mondo:0007409,cryptomicrotia-brachydactyly-excess fingertip arch syndrome,"['Cryptomicrotia-brachydactyly syndrome', 'Cryptomicrotia brachydactyly syndrome', 'Tonoki Ohura Niikawa syndrome', 'bilateral cryptomicrotia, brachytelomesophalangy, hypoplastic toe nails, and excess fingertip arch', 'CRYPTOMICROTIA-brachydactyly syndrome', 'Cryptomicrotia brachydactyly syndrome excess fingertip arch', 'Tonoki-Ohura-Niikawa syndrome']",,123560,1547,C1852454,,,,C536219,,,,
mondo:0007410,isolated cryptophthalmia,"['cryptophthalmos with microphthalmia and Peters anomaly', 'ankyloblepharon, simple', 'nonsyndromic cryptophthalmia', 'cryptophthalmos, unilateral or bilateral, isolated']",0111717,123570,91396,C1852453,"['-0.1084', '0.1411', '-0.2986', '-0.02408', '0.2338', '-0.11053', '-0.2128', '0.1631', '-0.3105', '-0.2058', '-0.1919', '8.72e-05', '-0.1086', '0.2024', '-0.2104', '0.1619', '0.5312', '-0.1588', '-0.1434', '-0.5776', '-0.2341', '0.2443', '0.08105', '-0.2374', '0.01636', '0.0661', '-0.2258', '-0.0777', '0.03354', '0.0756', '0.2524', '-0.03235', '-0.0445', '0.000506', '-0.001469', '0.05753', '0.2411', '-0.1042', '-0.087', '-0.2146', '0.353', '-0.1716', '-0.0593', '-0.3003', '0.02664', '-0.2401', '-0.279', '0.257', '0.0662', '0.084', '-0.03137', '-0.1327', '0.3904', '-0.0808', '-0.4258', '-0.2035', '0.4895', '0.2316', '-0.06396', '-0.0455', '0.0445', '-0.01224', '-0.1354', '-0.1262', '-0.02371', '-0.1192', '0.2123', '0.179', '-0.2573', '0.1536', '-0.1384', '0.2242', '0.05045', '-0.09753', '-0.1371', '0.1414', '0.11255', '0.09845', '0.1174', '-0.1887', '0.1447', '-0.02768', '0.4421', '0.3152', '0.1471', '-0.08295', '-0.1632', '0.5684', '-0.03683', '0.427', '0.07605', '0.2306', '0.2048', '0.1763', '0.9473', '-0.1178', '0.0752', '-0.558', '-0.11566', '0.2646']",,,C565138,,,,
mondo:0007411,"cutis laxa, autosomal dominant 1","['cutis laxa, autosomal dominant', 'autosomal dominant cutis laxa 1', 'cutis laxa, autosomal dominant 1', 'autosomal dominant cutis laxa caused by mutation in ELN', 'cutis laxa, autosomal dominant type 1', 'ELN autosomal dominant cutis laxa', 'ADCL1']",0070130,123700,,C3276539,,,,,,,,
mondo:0007412,Beare-Stevenson cutis gyrata syndrome,"['BSTVS', 'cutis gyrata-acanthosis nigricans-craniosynostosis syndrome', 'Beare-Stevenson cutis gyrata syndrome', 'cutis gyrata syndrome of Beare and Stevenson', 'Beare Stevenson syndrome', 'cutis gyrata - acanthosis nigricans - craniosynostosis', 'Beare-Stevenson syndrome']",0050660,123790,1555,C1852406,"['0.537', '0.338', '-0.269', '-0.4397', '0.1461', '-0.6914', '-0.02054', '0.579', '-0.1293', '-0.216', '-0.318', '-0.421', '-0.2878', '-0.4163', '-0.5425', '-0.2396', '0.213', '-0.1766', '-0.2703', '-0.861', '-0.03021', '-0.3293', '0.10956', '-0.05457', '0.3816', '0.4365', '-0.5474', '0.0363', '0.79', '-0.00849', '0.527', '-0.09534', '-0.2095', '0.0841', '-0.1897', '0.2876', '-0.1517', '-0.6143', '-0.2627', '-0.5215', '0.00981', '-0.02995', '0.3538', '-0.2915', '-0.1974', '-0.1454', '-0.0972', '-0.02264', '-0.0991', '0.699', '-0.2864', '-0.0815', '-0.3638', '0.3833', '-0.9766', '-0.03848', '-0.176', '0.4114', '0.09436', '0.7007', '-0.0794', '0.3516', '-0.527', '0.2646', '0.01726', '0.005974', '-0.521', '0.658', '-0.506', '1.378', '-0.362', '0.394', '0.605', '-0.1794', '0.011826', '-0.199', '0.1665', '-0.2805', '-0.423', '-0.4602', '-0.1857', '-0.2451', '-0.51', '-0.4336', '0.06976', '-0.1338', '-0.2996', '0.6113', '-0.1299', '0.352', '-0.2654', '0.6978', '0.0868', '0.3457', '0.678', '-0.158', '0.3857', '-0.1488', '0.44', '-0.3516']",C123813,,C565129,759.89,,,
mondo:0007413,Cyprus facial-neuromusculoskeletal syndrome,"['unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defects', 'CYPRUS facial neuromusculoskeletal syndrome']",,123853,2674,C1852396,,,,C536229,,,,
mondo:0007414,Gorham-Stout disease,"['Gorham-Stout disease', 'osteolysis massive', 'osteolysis, massive', 'Gorham syndrome', 'vanishing bone disease', 'cystic angiomatosis of bone, diffuse', 'Gorham disease', 'idiopathic massive osteolysis', 'cystic angiomatosis of bone diffuse', 'progressive massive osteolysis']",,123880,73,,,,,,733.99,,10071283,
mondo:0007415,mitochondrial complex III deficiency nuclear type 1,"['MC3DN1', 'mitochondrial complex III deficiency caused by mutation in BCS1L', 'BCS1L mitochondrial complex III deficiency', 'mitochondrial complex III deficiency, nuclear type 1', 'Complex 3 mitochondrial respiratory chain deficiency', 'mitochondrial Complex 3 deficiency, nuclear type 1', 'mitochondrial complex III deficiency']",0080111,124000,,,"['-0.03925', '0.0684', '-0.0008388', '0.00934', '0.02542', '-0.07135', '0.014336', '0.09064', '-0.08154', '-0.03845', '-0.0346', '-0.02107', '0.02332', '0.01541', '-0.03226', '-0.04556', '-0.01605', '-0.03497', '-0.03458', '-0.1447', '-0.0293', '-0.0506', '0.10583', '-0.0201', '0.02153', '-0.00783', '0.000277', '-0.01947', '0.003002', '-0.0383', '0.066', '0.00357', '0.0915', '0.04468', '0.012726', '-0.0677', '-0.003666', '-0.03296', '0.001765', '-0.0841', '0.02342', '-0.10126', '0.0319', '0.02228', '-0.02722', '-0.0712', '0.015495', '0.0508', '0.03915', '0.02725', '-0.01203', '-0.04086', '0.01962', '-0.012825', '-0.05005', '-0.03873', '0.0917', '-0.037', '-0.0971', '0.03268', '0.01502', '0.00998', '0.03912', '0.02971', '3.89e-05', '0.03078', '0.0838', '0.05463', '-0.07806', '0.07916', '-0.05237', '-0.002651', '0.01171', '-0.0579', '0.04028', '0.0598', '0.006073', '0.01378', '-0.04123', '-0.01225', '0.01379', '0.00965', '-0.00798', '0.05084', '-0.01001', '-0.0104', '0.05743', '0.09424', '0.1188', '0.01918', '0.02698', '0.0733', '-0.004234', '-0.01027', '0.1674', '0.0786', '0.074', '-0.11255', '-0.01823', '0.02684']",,,C565128,,,,
mondo:0007416,Balkan nephropathy,"['AAN', 'endemic nephropathy', 'Chinese herb endemic nephropathy', 'aristolochic acid nephropathy', 'BEN', 'nephropathia epidemica', 'DEFN', 'Danubian endemic familial nephropathy', 'Balkan endemic nephropathy']",3052,124100,,C4049993,,C123025,0007164,D001449,583.89,N15.0,,
mondo:0007417,Darier disease,"['DAR', 'Darier White disease', 'Darier disease', 'Darier-White disease', 'Darier^s disease', 'dar', 'keratosis follicularis', 'Darier disease, segmental', 'Darier disease, acral hemorrhagic type']",2734,124200,218,C0022595,"['0.56', '0.2109', '-0.4844', '-0.6846', '0.1251', '-0.1746', '0.1544', '-0.251', '-0.2776', '-0.1667', '-0.3127', '-0.05048', '0.0952', '-0.3894', '-0.2542', '0.5337', '0.444', '-0.5757', '-0.664', '-0.592', '-0.428', '-0.1973', '1.054', '0.114', '-0.3042', '0.05905', '-0.3057', '0.5625', '0.0605', '-0.4697', '0.619', '-0.3674', '0.0952', '0.135', '0.3792', '-0.2156', '0.11945', '-0.2627', '0.326', '0.0496', '0.3733', '-0.4248', '-0.2827', '-0.2346', '0.0784', '-0.2357', '0.1473', '-0.3345', '0.1252', '-0.07764', '-0.08044', '-0.4272', '0.162', '0.1012', '-0.1077', '0.02551', '0.708', '0.377', '-0.6177', '-0.481', '-0.165', '0.1238', '-0.6436', '-0.2744', '0.0619', '0.5166', '0.6587', '0.8193', '0.5244', '0.7266', '0.1232', '-0.6284', '-0.4023', '0.1356', '0.2222', '-0.0566', '0.009155', '-0.2302', '0.0651', '-0.6343', '-0.3704', '0.02167', '0.2175', '0.0735', '-0.1588', '0.2155', '-0.1405', '0.1248', '0.0352', '0.3098', '-0.6074', '0.3074', '-0.1703', '0.7705', '0.7095', '-0.0783', '-0.2028', '-0.4658', '-0.3042', '0.03268']",C84665,,D007644,757.39,,10023369,
mondo:0007418,Darwinian tubercle of pinna,"['Darwinian tubercle of pinna', 'Darwinian point of Pinna', 'Darwinian Notch']",,124400,,C2751189,,,,,,,,
mondo:0007420,autosomal dominant deafness - onychodystrophy syndrome,"['DDOD syndrome', 'deafness and onychodystrophy, dominant form', 'familial ectodermal dysplasia with sensori-neural deafness and other anomalies', 'deafness, congenital, and onychodystrophy, autosomal dominant', 'Ddod syndrome', 'Robinson Miller Bensimon syndrome', 'deafness-onychodystrophy syndrome, autosomal dominant', 'Robinson-Miller-Bensimon syndrome', 'deafness, congenital, with onychodystrophy, autosomal dominant', 'DDOD']",0080720,124480,79499,C2675730,"['0.2224', '-0.1015', '0.543', '-0.0007915', '0.4287', '-0.4812', '-0.0648', '0.7837', '-0.0343', '-1.154', '-0.2158', '-0.3918', '0.1915', '0.2356', '0.1777', '0.631', '0.5757', '-0.661', '-0.1611', '-0.6465', '-0.2296', '-0.3555', '0.342', '0.1697', '0.374', '-0.1165', '-1.023', '0.129', '0.545', '0.002838', '0.351', '-0.2085', '-0.3691', '0.195', '-0.1343', '-0.765', '-0.2852', '-0.4546', '0.1685', '0.02937', '0.6265', '-0.312', '0.2756', '-0.2744', '0.2451', '-0.721', '-0.3599', '0.2233', '-0.1192', '-0.1909', '0.06116', '0.05246', '-0.00915', '-0.0499', '-0.5874', '-0.2734', '-0.1821', '-0.002977', '-0.5273', '-0.07465', '-0.4392', '0.01188', '-0.2625', '0.5273', '-0.4878', '-0.06573', '-0.2267', '0.4685', '-0.1805', '0.4104', '-0.609', '-0.02783', '0.02454', '0.00804', '0.534', '0.1594', '0.301', '-0.4739', '-0.21', '0.0876', '0.006767', '0.3298', '0.2053', '0.7954', '-0.4954', '0.242', '-0.2307', '0.504', '-0.2448', '0.2803', '-0.05493', '0.87', '-0.000404', '0.1619', '0.2825', '0.0973', '0.158', '-1.112', '0.4229', '0.459']",,,,,,,
mondo:0007421,deafness-ear malformation-facial palsy syndrome,"['Sellars-Beighton syndrome', 'deafness, conductive stapedial, with EAR malformation and facial palsy']",,124490,3232,,,,,C565123,,,,
mondo:0007422,keratoderma hereditarium mutilans,"['keratoderma hereditarium mutilans', 'KHM', 'mutilating keratoderma', 'mutilating keratoderma plus deafness', 'mutilating keratoderma of Vohwinkel', 'VOWNKL', 'Vohwinkel syndrome', 'deafness, congenital, with KERATOPACHYDERMIA and constrictions of fingers and toes', 'PPK mutilans and deafness']",0111339,124500,494,,"['-0.1857', '0.1091', '0.142', '-0.2544', '0.10974', '-0.547', '-0.2988', '0.004032', '-0.2043', '0.03336', '-0.04584', '0.1782', '-0.2227', '-0.2135', '-0.06525', '-0.0672', '0.5684', '-0.3801', '0.0501', '-0.7856', '-0.10913', '-0.091', '0.2336', '0.1549', '0.2177', '0.4912', '-0.1827', '0.2043', '-0.04388', '-0.2059', '-0.0649', '-0.138', '0.141', '0.2394', '0.09955', '-0.2316', '-0.2418', '-0.3467', '-0.0887', '-0.188', '-0.1305', '-0.2429', '-0.05652', '0.2668', '0.076', '-0.1974', '-0.2172', '0.404', '0.02783', '-0.1334', '-0.3394', '0.11694', '0.2308', '-0.004124', '-0.3452', '-0.362', '0.4854', '0.006943', '-0.4092', '-0.1114', '0.02', '-0.03506', '-0.06934', '0.1171', '-0.06525', '0.04877', '0.2917', '0.645', '-0.1064', '0.339', '-0.4836', '-0.06537', '0.2178', '-0.287', '0.2622', '-0.01517', '0.09076', '-0.08856', '0.221', '-0.1919', '0.0486', '0.11', '0.0884', '0.2908', '0.0768', '0.0841', '-0.3457', '0.614', '0.03683', '0.3604', '0.279', '0.2205', '0.2654', '0.2793', '0.2869', '0.01805', '0.4639', '-0.402', '0.2644', '0.2369']",,,C536457,757.39,,,
mondo:0007423,"deafness, mid-tone neural","['deafness, mid-tone neural']",,124700,,C1852283,,,,C565122,,,,
mondo:0007424,autosomal dominant nonsyndromic hearing loss 1,"['Konigsmark syndrome', 'DIAPH1 autosomal dominant nonsyndromic deafness', 'DFNA1', 'deafness, autosomal dominant 1', 'deafness, autosomal dominant 1, with or without thrombocytopenia', 'deafness, autosomal dominant type 1', 'deafness, progressive Low tone', 'LFHL1', 'autosomal dominant nonsyndromic deafness type 1', 'autosomal dominant nonsyndromic deafness caused by mutation in DIAPH1', 'autosomal dominant nonsyndromic deafness 1', 'hereditary Low frequency hearing loss', 'autosomal dominant deafness 1', 'hereditary low frequency hearing loss 1']",0110541,124900,,C1852282,,,,C565121,,,,
mondo:0007425,"deafness, sensorineural, with peripheral neuropathy and arterial disease","['deafness, sensorineural, with peripheral neuropathy and arterial disease']",,124950,,C1852280,,,,C565120,,,,
mondo:0007426,"deafness, unilateral","['deafness, unilateral']",,125000,,C2607947,,,,C567079,,,,
mondo:0007427,deafness with anhidrotic ectodermal dysplasia,['deafness with anhidrotic ectodermal dysplasia'],,125050,,C1852279,,,,C565119,,,,
mondo:0007428,deafness-craniofacial syndrome,"['deafness-craniofacial syndrome', 'deafness craniofacial syndrome']",,125230,3241,C1852278,,,,C565118,,,,
mondo:0007429,"optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy","['dominant optic atrophy plus syndrome', 'optic atrophy plus syndrome', 'optic atrophy with or without deafness, ophthalmoplegia, myopathy, ataxia, and neuropathy', 'optic atrophy 1 and deafness']",,125250,3212,C3276549,,,,,,,,
mondo:0007430,dens evaginatus,['dens evaginatus'],,125280,,,,,,,,,,
mondo:0007431,dens in dente and palatal invaginations,['dens in dente and palatal INVAGINATIONS'],,125300,,C1852250,,,,C538211,,,,
mondo:0007432,cerebral arteriopathy with subcortical infarcts and leukoencephalopathy,"['cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy', 'CADASIL', 'Casil', 'dementia, hereditary multi-infarct type', 'cerebral arteriopathy with subcortical infaracts and leukoencephalopathy']",13945,,,,,,,,447.8,,,
mondo:0007433,dementia/parkinsonism with non-Alzheimer amyloid plaques,['dementia/parkinsonism with non-Alzheimer amyloid plaques'],,125320,,C1852223,,,,C565115,,,,
mondo:0007434,primary failure of tooth eruption,"['dental noneruption', 'posterior Openbite malocclusion, familial', 'PFE', 'unerupted second primary molar', 'primary failure of eruption, nonsyndromic', 'primary retention of teeth', 'failure of tooth eruption, primary']",0111341,125350,412206,C1852222,"['-0.083', '-0.08246', '0.10785', '0.003296', '0.0736', '-0.05347', '0.1642', '0.2805', '-0.3987', '0.1216', '-0.412', '-0.1432', '-0.0854', '0.2844', '-0.1666', '-0.10016', '0.05466', '-0.341', '-0.2925', '-0.5176', '-0.1355', '0.02507', '0.2979', '-0.01217', '0.1426', '-0.0962', '-0.2847', '0.05252', '0.2112', '-0.0862', '0.1674', '0.04404', '-0.2825', '-0.01666', '0.223', '0.00669', '0.06027', '-0.0968', '0.1732', '-0.2462', '0.207', '-0.02605', '0.02197', '-0.0434', '-0.2482', '0.04114', '-0.1858', '0.006393', '0.0909', '0.2144', '0.03534', '0.06064', '0.2177', '0.05722', '-0.3772', '-0.2074', '0.1886', '-0.2443', '-0.1921', '-0.11664', '0.342', '0.0788', '-0.1321', '-0.0581', '0.1188', '-0.0364', '0.4111', '0.4465', '0.0976', '0.1903', '-0.0978', '-0.0386', '0.2488', '-0.2551', '0.1407', '-0.03644', '0.08057', '-0.285', '-0.04126', '-0.1184', '-0.1183', '-0.10376', '0.01418', '0.1569', '0.09357', '0.1084', '-0.1356', '0.010956', '0.2888', '0.0979', '-0.1339', '0.10126', '-0.0719', '0.4626', '0.4148', '-0.0639', '0.2229', '-0.3987', '0.0568', '0.2014']",,,C565114,,,,
mondo:0007435,dentatorubral-pallidoluysian atrophy,"['DRPLA', 'Dentatorubropallidoluysian atrophy', 'dentatorubral pallidoluysian atrophy', 'Naito-Oyanagi disease', 'dentatorubral-pallidoluysian atrophy', 'myoclonic epilepsy with choreoathetosis', 'ataxia, chorea, seizures, and dementia', 'Naito Oyanagi disease', 'haw River syndrome', 'NOD']",0060162,125370,101,C0751781,"['0.11163', '0.648', '-0.1704', '-0.2734', '-0.03336', '-0.551', '0.3782', '0.4585', '-0.6655', '-0.3215', '-0.3076', '0.0323', '-0.2352', '-0.9526', '1.116', '-0.267', '0.5728', '-0.785', '0.2664', '-0.3635', '0.04224', '-0.3455', '0.2822', '-0.2913', '-0.08875', '0.2476', '-0.4146', '-0.419', '-0.582', '0.0376', '0.545', '-0.2324', '0.276', '-0.234', '-0.1338', '0.2627', '-0.481', '-0.455', '-0.09515', '-0.1421', '0.3328', '-0.751', '-0.1033', '0.2842', '0.0669', '-0.46', '0.3362', '0.3594', '0.06165', '0.03656', '0.576', '0.5703', '-1.132', '-0.5356', '-0.11743', '0.1661', '0.3108', '-0.3252', '-0.07404', '0.1345', '-0.01611', '-0.04868', '0.4167', '0.0084', '-0.53', '0.2308', '0.4229', '0.4958', '-0.5825', '0.06525', '0.313', '0.3818', '0.1766', '0.2194', '0.5605', '0.467', '0.0734', '-0.2054', '-0.201', '-0.4265', '-0.0859', '-0.2954', '-0.4375', '0.612', '0.1699', '-0.1794', '0.1322', '0.7095', '0.6357', '0.159', '0.1794', '0.4373', '-0.0408', '-0.0361', '0.567', '0.3442', '0.3809', '0.1703', '0.2393', '0.10126']",C7636,,D020191,333.99,,,
mondo:0007436,dentin dysplasia type I,"['rootless teeth', 'DTDP1', 'dentin dysplasia, type 1', 'dentin dysplasia, type I', 'dentin dysplasia, Shields type 1', 'dentin dysplasia, type I, with extreme microdontia and misshapen teeth', 'radicular dentin dysplasia', 'dentin dysplasia, type i, with microdontia and misshapen teeth', 'DD-I']",,125400,99789,C0399379,"['-0.06042', '0.04678', '0.2559', '-0.1791', '0.2676', '0.0347', '0.2001', '0.584', '-0.1064', '0.010155', '-0.3022', '-0.1444', '-0.4036', '0.05917', '0.0783', '0.0779', '0.3755', '-0.2251', '0.2489', '-1.094', '-0.63', '0.2141', '0.809', '0.00593', '0.4324', '0.3428', '-0.5913', '0.0004652', '0.007793', '0.03128', '-0.2605', '0.1843', '-0.293', '-0.1278', '0.05194', '-0.02602', '0.4692', '-0.332', '0.3738', '-0.885', '0.2', '-0.167', '0.00867', '-0.2086', '-0.422', '-0.0499', '-0.2822', '0.07635', '0.3792', '0.00493', '0.6', '-0.178', '0.7305', '-0.4797', '-0.508', '-0.3462', '0.1247', '-0.7764', '-0.1566', '-0.1487', '0.2817', '0.1814', '0.1738', '0.08844', '0.1194', '0.3481', '0.4766', '0.0909', '-0.111', '0.1536', '-0.1598', '-0.2246', '0.3066', '-0.3833', '0.2996', '0.11224', '-0.2625', '-0.05612', '-0.2363', '-0.03094', '-0.2874', '-0.543', '-0.2332', '0.04785', '-0.1528', '0.09875', '-0.10944', '-0.0994', '0.1766', '0.05023', '-0.4458', '0.2041', '-0.2094', '0.8354', '0.71', '0.1543', '0.0671', '-0.7866', '0.415', '0.1521']",,,C538215,520.5,,,
mondo:0007437,dentin dysplasia type II,"['anomalous dysplasia of dentin', 'dentin dysplasia, type II', 'DTDP2', 'Dtdp2', 'pulpal dysplasia', 'dentin dysplasia, type 2', 'DD-II', 'coronal dentin dysplasia', 'pulp stones', 'dentin dyspalsia, Shields type 2', 'dentin dysplasia, Shields type 2', 'dentin dysplasia, coronal']",,125420,99791,,"['0.0387', '0.0757', '0.5513', '-0.0648', '0.377', '0.1729', '0.159', '0.5522', '-0.07587', '0.408', '-0.323', '-0.481', '-0.3518', '0.2952', '-0.09424', '-0.0654', '0.00844', '-0.4148', '0.1901', '-1.1455', '-0.1063', '0.1697', '0.614', '0.0846', '0.1893', '0.2666', '-0.988', '-0.0332', '0.1197', '-0.0682', '-0.05795', '0.7236', '-0.4307', '-0.0749', '0.08386', '-0.4514', '-0.04095', '-0.857', '0.564', '-1.056', '1.149', '-0.2034', '-0.3423', '0.1807', '-0.358', '-0.139', '0.04935', '0.05533', '0.1759', '-0.2471', '1.02', '-0.36', '0.3008', '-0.4875', '-1.16', '-0.0757', '0.1427', '-0.6475', '-0.1254', '0.03253', '0.4036', '0.2922', '-0.305', '-0.1378', '-0.254', '0.04626', '0.3745', '0.1466', '-0.07245', '0.2656', '-0.7725', '-0.0503', '0.10486', '-0.6934', '0.0732', '-0.1071', '-0.37', '-0.352', '-0.3418', '-0.3613', '-0.6255', '-0.08514', '-0.3074', '0.09674', '-0.55', '-0.0896', '-0.2322', '-0.04074', '0.533', '0.1504', '-0.5015', '0.5015', '-0.159', '0.859', '0.6597', '0.315', '0.09546', '-0.557', '0.3162', '0.03041']",,,,520.5,,,
mondo:0007438,dentin dysplasia-sclerotic bones syndrome,"['dentin dysplasia sclerotic bones', 'dentin dysplasia with sclerotic bones', 'sclerotic bones with dentin dysplasia']",,125440,99792,C1852201,,,,C538213,,,,
mondo:0007439,deoxyribose-5-phosphate aldolase deficiency,['deoxyribose-5-phosphate aldolase deficiency'],,125460,,C1852200,,,,C565112,,,,
mondo:0007440,major affective disorder 1,"['bipolar affective disorder', 'manic-depressive psychosis', 'MAJOR affective disorder 1', 'manic-depressive psychosis, autosomal', 'major affective disorder 1', 'MAFD1']",0080220,125480,,,,,,C565111,,,,
mondo:0007441,dentinogenesis imperfecta type 2,"['DGI1', 'DGI-II', 'dentinogenesis imperfecta, Shields type II', 'dentinogenesis imperfecta 1', 'dentinogenesis imperfecta type 1', 'opalescent teeth without osteogenesis imperfecta', 'DGI-2', 'dentinogenesis imperfecta, Shields type 2', 'Capdepont teeth', 'DI-2', 'dentinogenesis imperfecta without osteogenesis imperfecta', 'opalescent dentin']",,125490,166260,,"['0.2893', '0.0677', '0.4092', '0.1349', '0.01305', '-0.0684', '0.2605', '0.574', '-0.3523', '0.2764', '-0.368', '-0.3667', '-0.1724', '0.1664', '-0.0743', '-0.1882', '0.3467', '-0.2644', '0.0004964', '-0.903', '-0.219', '-0.11053', '0.3994', '-0.0698', '0.3', '0.211', '-0.788', '0.12384', '-0.02571', '-0.44', '-0.203', '0.4438', '-0.3926', '-0.1503', '0.3174', '-0.3516', '0.327', '-0.3582', '0.53', '-0.5254', '0.586', '-0.3738', '-0.1646', '-0.345', '-0.4504', '0.1974', '-0.1266', '0.104', '0.01119', '0.1564', '0.5796', '-0.3862', '0.6367', '-0.513', '-0.716', '-0.3164', '-0.02371', '-0.2913', '-0.005688', '-0.251', '0.2239', '-0.04578', '-0.211', '-0.2678', '-0.05362', '-0.07526', '-0.05106', '0.4102', '0.131', '0.1962', '-0.335', '-0.297', '0.4', '-1.0205', '0.4685', '-0.1146', '-0.3396', '-0.1338', '-0.2349', '-0.1823', '0.1721', '-0.3003', '-0.2805', '0.217', '-0.3923', '0.502', '-0.2467', '0.1772', '0.6616', '-0.01003', '-0.1969', '0.2028', '-0.1505', '0.7607', '0.6646', '-0.0871', '0.00507', '-0.8765', '0.07404', '-0.0738']",,,,,,,
mondo:0007442,dentinogenesis imperfecta type 3,"['brandywine type dentinogenesis imperfecta', 'dentinogenesis imperfecta type III', 'dentinogenesis imperfecta, Shields type III', 'DGI-III', 'dentinogenesis imperfecta, Shields type 3', 'dentinogenesis imperfecta Shields type 3']",,125500,166265,,"['0.235', '0.07477', '0.3555', '-0.1404', '0.3389', '0.1047', '-0.1747', '0.3467', '-0.05847', '0.2957', '-0.2261', '-0.2074', '-0.4155', '-0.0345', '-0.211', '-0.1498', '0.3184', '-0.4026', '-0.0979', '-0.561', '-0.478', '0.02605', '0.786', '-0.5527', '0.201', '0.3567', '-0.685', '-0.2196', '0.09174', '-0.2585', '0.1545', '0.2996', '-0.487', '-0.1381', '0.378', '-0.52', '0.0556', '-0.2778', '0.1494', '-0.677', '0.416', '-0.8115', '-0.1655', '-0.161', '-0.5107', '-0.008026', '0.4236', '0.63', '0.4463', '0.10425', '0.2703', '-0.4558', '0.1747', '-0.1332', '-0.811', '-0.152', '0.306', '-0.568', '-0.2952', '0.05505', '0.257', '0.2139', '-0.453', '-0.11914', '0.1305', '-0.0455', '0.348', '0.4106', '-0.0407', '0.1334', '-0.28', '0.4329', '0.4458', '-0.7637', '0.254', '0.6216', '-0.2905', '0.0162', '-0.3254', '-0.02275', '0.09814', '-0.1276', '0.01862', '-0.03497', '-0.2311', '-0.5103', '-0.1371', '0.399', '0.549', '-0.1644', '-0.06256', '0.491', '0.2334', '0.4688', '0.448', '0.1521', '0.2905', '-0.4421', '-0.0045', '-0.4753']",,,C538216,520.5,,,
mondo:0007443,congenital unilateral hypoplasia of depressor anguli oris,"['Cayler cardiofacial syndrome', 'asymmetric crying facies', 'facial paresis, partial, unilateral', 'isolated asymmetric crying facies', 'depressor anguli oris muscle, hypoplasia of']",,125520,1166,,,,,,759.89,,,
mondo:0007444,"dermal Ridges, patternless","['dermal Ridges, patternless']",,125540,,C1852160,,,,C565109,,,,
mondo:0007445,dermatopathia pigmentosa reticularis,"['DPR', 'dermatopathia pigmentosa reticularis']",0111342,125595,86920,,"['-0.1896', '0.2146', '0.037', '-0.2048', '0.02657', '-0.3816', '-0.2152', '0.1387', '0.01828', '-0.08716', '-0.223', '-0.00736', '-0.2856', '-0.0671', '-0.2412', '0.0121', '0.3616', '-0.2285', '-0.1481', '-0.7705', '-0.136', '-0.02931', '0.1757', '0.03607', '0.04242', '0.3035', '-0.3057', '0.0679', '0.00986', '-0.2698', '0.1821', '-0.0638', '-0.01238', '0.3057', '0.2742', '0.04303', '-0.2856', '-0.1683', '-0.0387', '-0.1504', '-0.007584', '-0.03467', '-0.11255', '-0.1857', '-0.1293', '-0.168', '-0.2297', '0.1318', '-0.04733', '0.0002404', '-0.1624', '-0.02045', '0.2446', '0.10974', '-0.272', '-0.0665', '0.359', '-0.05078', '-0.2003', '-0.0673', '0.2484', '0.0668', '-0.1724', '-0.1676', '0.01854', '0.0511', '0.393', '0.552', '0.02632', '0.5073', '-0.2563', '-0.1715', '0.1733', '-0.04654', '-0.00676', '-0.3455', '0.09845', '-0.06146', '0.05484', '-0.012', '0.01266', '-0.03976', '0.1562', '0.201', '-0.006565', '-0.0348', '-0.2346', '0.2632', '0.2666', '0.239', '0.3853', '0.1547', '0.1505', '0.3184', '0.359', '-0.0734', '0.3867', '-0.2893', '0.2393', '0.2291']",,,C535374,,,,
mondo:0007446,dermatosis papulosa nigra,"['dermatosis papulosa nigra', 'dermatosis papulosa nigra (morphologic abnormality)']",4400,125600,,C0011645,,C2984,1000686,C562379,709.8,L82,,
mondo:0007447,autosomal dominant vibratory urticaria,"['DDU', 'vibratory angioedema', 'dermodistortive urticaria', 'angioedema, vibratory', 'VBU', 'vibratory urticaria, autosomal dominant']",,193050,493348,C1852146,,,,C536347,995.1,,,
mondo:0007448,familial dermatographia,"['dermographism', 'DDU', 'familial dermographism', 'vibratory angioedema', 'dermatographic urticaria', 'familial dermatographism', 'Dermatographism, familial', 'VBU', 'dermatographia', 'dermo-distortive urticaria', 'dermographism, familial', 'vibratory urticaria', 'Dermodistortive urticaria']",743,125635,,,,,1000685,C536612,708.3,L50.3,,
mondo:0007449,dermo-odonto dysplasia,"['DERMOODONTODYSPLASIA', 'dermo-odonto-dysplasia', 'ectodermal dysplasia, hair-nail-Tooth type']",,125640,1660,C4303591,,,,C565103,,,,
mondo:0007450,neurohypophyseal diabetes insipidus,"['ADH deficiency', 'Arginine vasopressin deficiency', 'hereditary CDI', 'hereditary neurogenic diabetes insipidus', 'vasopressin deficiency', 'hereditary central diabetes insipidus', 'pituitary diabetes insipidus', 'diabetes insipidus, cranial type', 'neurogenic diabetes insipidus', 'AVP deficiency', 'diabetes insipidus of pituitary gland', 'vasopressin defective diabetes insipidus', 'pituitary gland diabetes insipidus', 'diabetes insipidus, primary central', 'diabetes insipidus, neurohypophyseal', 'antidiuretic hormone deficiency']",12388,125700,30925,,"['0.7393', '-0.1621', '0.1176', '0.7954', '-0.4336', '-0.929', '-0.3958', '0.9146', '0.26', '-0.5195', '0.04346', '-0.02261', '0.2903', '0.2072', '-0.937', '-0.366', '0.5767', '0.3257', '-0.0793', '-0.5303', '0.1831', '-0.1279', '0.1539', '0.1159', '-0.7026', '-0.3586', '0.06366', '-0.1697', '0.38', '-0.501', '1.001', '-0.6987', '0.3425', '-0.2357', '-0.2046', '0.4497', '-0.7764', '0.4863', '0.010704', '-0.208', '0.1635', '0.3813', '0.2712', '0.4746', '-0.408', '-0.419', '0.417', '-0.11084', '0.03232', '0.3682', '0.3596', '-0.3635', '0.7827', '-0.85', '-0.03564', '0.2003', '-0.04987', '-0.6885', '-1.034', '0.594', '-0.4192', '0.626', '-0.1115', '0.1708', '-0.05508', '0.892', '-0.318', '0.624', '-0.9873', '0.1964', '0.4822', '0.357', '0.09503', '-0.2595', '0.712', '0.524', '-0.664', '1.169', '-0.3953', '-0.1044', '0.1837', '-0.00477', '0.03592', '-0.545', '0.10016', '0.3606', '0.1024', '0.5454', '0.7095', '0.1763', '0.677', '0.3638', '0.0889', '-0.1497', '1.242', '0.3296', '-0.1927', '-0.0767', '-0.4565', '0.02173']",C84933,,,,,,
mondo:0007451,"diabetes insipidus, nephrogenic, autosomal","['diabetes insipidus, nephrogenic, autosomal', 'diabetes insipidus, nephrogenic, type 2', 'diabetes insipidus, nephrogenic, 2']",0081061,125800,,C1563706,,,,,,,,
mondo:0007452,maturity-onset diabetes of the young type 1,"['MODY HNF4A related', 'diabetes mellitus MODY type 1', 'HNF4A-associated monogenic diabetes', 'MODY1', 'diabetes mellitus type 2', 'maturity-onset diabetes of the young, type 1', 'mild juvenile diabetes mellitus', 'MODY type 1', 'maturity onset diabetes of the Young, type 1', 'hepatocyte nuclear Factor 4-Alpha associated monogenic diabetes', 'type 1 maturity-onset diabetes of the young', 'MODY, type 1', 'MODY, type I']",0111099,125850,,C1852093,,C129744,,C565101,,,,
mondo:0007453,maturity-onset diabetes of the young type 2,"['GCK-associated diabetes mellitus', 'MODY, type 2', 'diabetes mellitus MODY type 2', 'glucokinase-associated diabetes mellitus', 'GCK maturity-onset diabetes of the young (disease)', 'MODY 2 monogenic diabetes type 2', 'MODY glucokinase-related', 'MODY2', 'MODY, glucokinase-related', 'maturity onset diabetes of the Young, type 2', 'type 2 maturity-onset diabetes of the young', 'MODY, type II', 'MODY type 2', 'maturity-onset diabetes of the young, type 2']",0111100,125851,,C0085207,,C129741,,,,,,
mondo:0007454,type 1 diabetes mellitus 2,"['type 1 diabetes mellitus caused by mutation in INS', 'IDDM2', 'diabetes mellitus, insulin-dependent, 2', 'insulin-dependent diabetes mellitus 2', 'diabetes mellitus, insulin-dependent, type 2', 'INS type 1 diabetes mellitus']",0110741,125852,,C1852092,,,,C565100,,,,
mondo:0007456,"diarrhea, glucose-stimulated secretory, with common variable immunodeficiency","['diarrhea, glucose-stimulated secretory, with common variable immunodeficiency']",,125890,,C1852087,,,,C565099,,,,
mondo:0007457,"diastema, dental medial","['diastema, dental medial']",,125900,,,,,,C565098,,,,
mondo:0007458,"digitotalar dysmorphism; ulnar drift, hereditary","['digitotalar dysmorphism', 'ulnar drift, hereditary']",,126050,,,,,,,,,,
mondo:0007459,"dilution, pigmentary","['hypomelanotic disorder', 'dilution, pigmentary', 'hypopigmentation', 'Albinoidism, oculocutaneous, autosomal dominant', 'albinism, partial']",,126070,,C1876214,,,,C566872,,,,
mondo:0007460,"discrimination, Two-point, reduction 1N","['discrimination, TWO-point, reduction IN', 'discrimination, Two-point, reduction type 1N', 'sensory discrimination']",,126180,,,,,,,,,,
mondo:0007461,short stature-valvular heart disease-characteristic facies syndrome,['disproportionate short stature with ptosis and valvular heart lesions'],,126190,2868,C1852073,,,,C565094,,,,
mondo:0007462,"multiple sclerosis, susceptibility to","['MS', 'disseminated sclerosis']",,,,,,,,,,,,
mondo:0007463,distal osteosclerosis,"['osteosclerosis, distal', 'distal osteosclerosis']",,126250,,C1852063,,,,C565093,,,,
mondo:0007465,distichiasis with congenital anomalies of the heart and peripheral vasculature,"['distichiasis with congenital anomalies of the heart and peripheral vasculature', 'distichiasis-congenital heart defects-peripheral vascular anomalies syndrome']",,126320,1683,C1852062,,,,C565092,,,,
mondo:0007466,"DNA, satellite, 3","['D1Z1', 'DNA, satellite, type 3', 'DNA, satellite, III', 'HS3']",,126370,,,,,,,,,,
mondo:0007467,"DNA, low-repetitive sequences of","['DNA, low-repetitive sequences of', 'repetitive sequence DNA']",,126390,,,,,,,,,,
mondo:0007469,double nail for fifth toe,"['Double nails on the fifth toe', 'fifth toe, double nails', 'double nail for fifth toe']",,126500,,,,,,C565090,,,,
mondo:0007470,calvarial doughnut lesions-bone fragility syndrome,"['calvarial doughnut lesions with bone fragility with or without spondylometaphyseal dysplasia', 'doughnut lesions of skull, familial', 'familial doughnut lesions of skull']",0080721,126550,85192,C1852022,"['-0.5776', '-0.03793', '0.2429', '-0.51', '0.5874', '0.1454', '-0.274', '0.462', '-0.2028', '0.0955', '-0.435', '0.06494', '-0.1859', '-0.3203', '0.0399', '0.412', '0.3557', '-0.0631', '-0.37', '-0.807', '0.04968', '-0.2664', '0.5713', '-0.1231', '0.3228', '0.65', '-0.06616', '-0.1644', '-0.1302', '-0.154', '0.3396', '-0.1625', '0.1946', '0.4211', '0.07404', '-0.06104', '-0.2305', '-0.4995', '0.0642', '-0.5293', '0.1306', '-0.173', '0.408', '-0.5127', '0.0417', '-0.4734', '0.0704', '0.2937', '-0.1906', '-0.3796', '0.2886', '-0.1603', '0.4124', '0.214', '-0.556', '-0.2842', '0.1814', '-0.285', '-0.3667', '-0.05252', '0.534', '-0.09546', '-0.3877', '-0.529', '-0.1958', '-0.11914', '0.325', '0.5674', '-0.368', '0.08685', '-0.2433', '-0.06226', '-0.1735', '-0.3005', '0.0532', '0.03546', '-0.0136', '0.342', '0.301', '-0.5083', '0.04996', '0.3315', '0.1335', '0.2303', '-0.1959', '-0.0529', '0.1787', '0.31', '-0.001029', '-0.2119', '0.1567', '0.3179', '-0.2585', '0.04474', '0.5845', '0.529', '0.4426', '-0.53', '0.348', '0.01932']",,,C565089,,,,
mondo:0007471,Doyne honeycomb retinal dystrophy,"['drusen, radial, autosomal dominant', 'Malattia leventinese', 'dominant drusen', 'familial drusen', 'dominant radial drusen', 'DHD', 'DHRD', 'Doyne honeycomb retinal dystrophy', 'Doyne honeycomb degeneration of retina']",0060745,126600,75376,CN205694,"['-0.5176', '0.2312', '-0.1473', '0.2634', '0.44', '-0.4146', '-0.342', '-0.02667', '-0.4824', '-0.0446', '0.2546', '-0.1392', '-0.6377', '-0.148', '-0.02536', '-0.1277', '0.05524', '-0.2722', '0.323', '-0.692', '-0.12054', '-0.1698', '0.0643', '0.174', '0.10425', '0.1564', '-0.389', '-0.05765', '-0.07855', '0.3757', '0.824', '-0.2646', '-0.1418', '0.1277', '0.1367', '0.4216', '-0.03848', '-0.0418', '0.28', '-0.4358', '0.3572', '-0.3572', '0.01816', '-0.156', '-0.1936', '0.1113', '-0.09875', '-0.06024', '0.2224', '-0.0964', '0.523', '0.363', '0.095', '-0.4382', '0.1874', '-0.4905', '0.738', '0.4363', '-0.6377', '-0.1381', '0.00195', '-0.01296', '0.1465', '0.003944', '-0.1238', '0.0514', '0.5073', '0.67', '-0.135', '0.6724', '-0.1903', '-0.08514', '0.3274', '0.437', '0.2144', '-0.2305', '-0.0776', '0.3345', '0.1675', '-0.564', '0.1864', '-0.159', '0.1313', '0.3442', '-0.1482', '-0.2517', '0.05786', '0.1675', '0.2625', '0.2434', '0.005695', '0.512', '0.1412', '-0.02155', '0.3179', '-0.1382', '0.1294', '-0.368', '-0.0727', '0.323']",,,,,H35.5,,
mondo:0007472,basal laminar drusen,"['drusen, early adult-onset, grouped', 'early adult-onset grouped drusen', 'drusen, cuticular', 'basal laminar drusen', 'cuticular drusen', 'drusen of Bruch membrane']",0060746,126700,,C0730295,,,,C563034,,H35.5,,
mondo:0007473,Duane retraction syndrome,"['Duane retraction syndrome', 'Duane^s syndrome', 'Stilling-Turk-Duane syndrome', 'Duane anomaly', 'DRS', 'DURS', 'retraction syndrome', 'Duane syndrome']",12557,,233,C0013261,"['0.228', '-0.4443', '-0.2778', '-0.02126', '0.6533', '-0.03622', '0.2825', '0.82', '-0.6523', '-0.0448', '0.04578', '0.1469', '-0.0641', '0.03366', '-0.621', '0.05426', '0.8867', '-0.9243', '0.4175', '-0.5386', '-0.4045', '-0.005707', '0.495', '-0.2542', '-0.01985', '0.259', '-0.1785', '0.1681', '0.1874', '0.638', '-0.4873', '0.327', '0.666', '0.044', '-0.3608', '-0.449', '0.003336', '-0.396', '0.56', '-0.4072', '0.643', '0.2893', '0.1044', '-0.2391', '0.4636', '0.0922', '0.2134', '0.2017', '0.2974', '0.4128', '-0.11115', '-0.4653', '0.1545', '-0.7837', '-0.4084', '0.09814', '0.11224', '-0.386', '-0.3477', '-0.1599', '0.2457', '0.8403', '0.6543', '0.3818', '-0.524', '-0.2612', '0.0863', '0.2712', '0.4412', '0.4238', '-0.2659', '0.5605', '-0.3157', '-0.576', '0.4976', '0.642', '0.4297', '-0.2815', '-1.098', '-0.06494', '0.6206', '-0.3433', '-0.0413', '1.01', '-0.833', '0.07935', '0.3', '0.454', '0.1329', '0.1714', '-0.548', '0.3618', '0.3938', '0.5117', '0.698', '-0.01356', '0.68', '-0.0643', '-0.0359', '0.522']",C84678,,D004370,378.71,,10013799,
mondo:0007474,duodenal ulcer due to antral G-cell hyperfunction,"['hypergastrinemic, hyperpepsinogenemic duodenal ulcer', 'duodenal ulcer due to antral G-cell hyperfunction']",,126840,,C1852009,,,,C535721,,,,
mondo:0007475,"duodenal ulcer, hyperpepsinogenemic 1","['duodenal Ulcer, hyperpepsinogenemic type 1', 'duodenal ulcer, hyperpepsinogenemic I']",,126850,,C1852008,,,,C565086,,,,
mondo:0007476,familial Dupuytren contracture,"['plantar fibromas', 'Dupuytren contracture 1', 'plantar fibromatosis, familial', 'Dupuytren contracture']",,126900,79142,,,,,,,,,
mondo:0007477,3-M syndrome,"['three M syndrome', 'three-M slender-boned nanism', '3M1', '3-MSBN', 'Yakut short stature syndrome', 'Le Merrer syndrome', 'Miller-McKusick-Malvaux syndrome', 'gloomy face syndrome', 'dolichospondylic dysplasia', '3M syndrome', 'dwarfism with tall vertebrae', '3-M syndrome', 'gloomy face syndrome Yakut short stature syndrome, included', 'Dolichospondylic dysplasia', 'three M syndrome 1']",0060241,,2616,,"['-0.3882', '-0.07904', '0.1022', '-0.325', '0.1868', '-0.3003', '0.5527', '1.129', '-0.835', '-0.8726', '0.508', '0.3733', '0.501', '0.01685', '0.207', '-0.011086', '0.614', '-0.1619', '-0.72', '-0.5366', '-0.3186', '-0.0374', '0.717', '-0.5444', '0.1858', '0.03041', '-0.1025', '-0.4082', '0.000226', '-0.3035', '0.5166', '-0.3318', '0.229', '0.3232', '-0.2725', '0.4058', '0.459', '0.02728', '-0.0897', '0.3005', '0.315', '-0.196', '0.001123', '-0.097', '0.1896', '-0.1477', '-0.401', '-0.1247', '0.0765', '-0.036', '-0.299', '-0.518', '-0.4768', '0.2893', '-0.5854', '0.1396', '-0.3623', '-0.461', '0.02254', '0.1527', '0.4648', '-0.2205', '-0.6807', '0.2322', '0.1124', '0.2722', '-0.013374', '0.1693', '-0.02118', '0.595', '0.2125', '0.5063', '0.01139', '-0.3188', '0.1512', '-0.1198', '-0.0546', '-0.256', '-0.7593', '-0.1339', '-0.00772', '0.0846', '-0.4832', '0.06247', '-0.51', '0.4429', '-0.5127', '-0.4456', '0.3892', '0.335', '0.3755', '0.3496', '-0.751', '0.2527', '0.533', '-0.01782', '0.1714', '-0.5195', '0.251', '0.06226']",,,C535314,756.59,,,
mondo:0007478,autosomal dominant Kenny-Caffey syndrome,"['KCS2', 'Kenny-Caffey syndrome type 2', 'dwarfism, cortical thickening of tubular bones and transient hypocalcemia', 'Kenny-Caffey syndrome, autosomal dominant', 'Kenny syndrome', 'dwarfism, cortical thickening of tubular bones, and transient hypocalcemia', 'Kenny-Caffey syndrome, type 2']",0080723,127000,93325,CN031291,"['-0.618', '0.55', '0.8384', '-0.623', '0.3176', '0.02818', '-0.1954', '0.6426', '-0.7974', '-0.4824', '-0.2979', '0.06934', '-0.08905', '-0.1339', '-0.2593', '-0.10144', '0.562', '-0.2532', '0.02232', '-0.851', '0.2488', '-0.01775', '0.2166', '-0.1221', '0.2622', '0.2817', '-0.183', '0.1167', '0.5747', '0.1523', '-0.423', '0.04504', '0.2233', '-0.1066', '-0.3171', '-0.1619', '0.281', '0.1466', '0.095', '-0.3623', '0.4993', '-0.0548', '0.3916', '-0.1277', '0.144', '-0.637', '0.2852', '0.1986', '0.66', '-0.0619', '0.2769', '0.2705', '-0.01154', '-0.2024', '-0.3574', '-0.814', '0.1791', '0.2834', '-0.2732', '0.302', '0.2815', '-0.0186', '-0.4211', '-0.267', '0.3008', '-0.11005', '0.2717', '0.3967', '-0.5264', '-0.02611', '-0.5034', '0.146', '0.418', '-0.3608', '-0.3987', '0.2014', '0.1864', '0.1598', '-0.1641', '0.2776', '-0.11597', '0.3555', '-0.0802', '0.00366', '-0.1404', '0.007538', '0.2303', '0.2009', '0.4863', '0.5405', '-0.5747', '0.561', '0.011635', '-0.10425', '0.932', '0.01058', '0.4631', '-0.1873', '0.4983', '0.276']",C130993,,,,,,
mondo:0007479,"dwarfism, Levi type","['dwarfism, Levi type', 'snub-nosed type of dwarfism', 'dwarfism Levi type', 'dwarfism Levi^s type']",,127100,,C1851994,,,,C565081,,,,
mondo:0007480,dwarfism with stiff joints and ocular abnormalities,"['Moore-Federman syndrome', 'dwarfism with stiff joints and ocular abnormalities']",,127200,2569,,,,,C535724,759.89,,,
mondo:0007481,Leri-Weill dyschondrosteosis,"['Leri Weill dyschondrosteosis', 'Léri-Weill dyschondrosteosis', 'Leri-Weill dyschondrostosis', 'Leri-Weill syndrome', 'Leri-Weill dyschondrosteosis, Pseudoautosomal dominant', 'Léri-Weill syndrome', 'dyschondrosteosis', 'Leri-Weill dyschondrosteosis', 'LWD', 'Madelung deformity', 'DCo']",0060847,127300,240,C0265309,"['-1.021', '0.02695', '0.11444', '-0.271', '0.155', '-0.284', '0.609', '0.573', '-0.4775', '-0.5156', '0.2434', '0.545', '0.5215', '0.5054', '0.1493', '-0.000647', '0.3938', '-0.09863', '-0.814', '-0.7437', '0.0826', '-0.11017', '0.2788', '-0.1667', '0.2217', '0.231', '0.445', '-0.04733', '-0.2542', '-0.1349', '0.504', '-0.51', '-0.11115', '0.2798', '-0.02025', '-0.502', '0.2979', '-0.6924', '0.1844', '0.0923', '-0.09283', '-0.2878', '0.531', '-0.11334', '0.3542', '-0.502', '-0.0771', '-0.11316', '0.395', '0.002806', '-0.2244', '-0.509', '-0.1642', '0.00406', '-0.2389', '-0.4448', '-0.0563', '-0.1384', '-0.2954', '-0.1493', '0.5117', '-0.0699', '-0.4353', '-0.432', '-0.587', '0.523', '0.236', '0.3774', '0.0896', '-0.2363', '-0.3284', '-0.4932', '0.5073', '-0.1242', '0.662', '0.07184', '-0.1565', '-0.2118', '-0.2094', '-0.6797', '0.3218', '0.0001509', '0.3042', '0.1735', '-0.2152', '0.2566', '0.02657', '-0.1147', '0.489', '0.2408', '-0.3032', '-0.2148', '-0.8833', '0.37', '-0.07117', '-0.219', '0.982', '-0.7666', '0.3728', '0.3406']",C126560,,,756.59,,,
mondo:0007482,dyschondrosteosis-nephritis syndrome,"['mesomelic shortening and hereditary nephritis', 'dyschondrosteosis and nephritis', 'dyschondrosteosis nephritis']",,127350,1765,C1851986,,,,C565080,,,,
mondo:0007483,dyschromatosis symmetrica hereditaria,"['dyschromatosis symmetrica hereditaria', 'reticulate acropigmentation of Dohi', 'acropigmentation of Dohi', 'dyschromatosis symmetrica hereditaria 1', 'familial reticulate acropigmentation of Dohi', 'DSH', 'DSH1', 'symmetric dyschromatosis of the extremities', 'RAD']",0060257,127400,41,C0406775,"['-0.4697', '0.151', '-0.3188', '-0.283', '0.3657', '-0.7007', '-0.3757', '0.1481', '-0.4363', '-0.0386', '-0.4272', '0.4949', '0.128', '-0.1373', '0.1489', '0.38', '0.176', '-0.2742', '-0.1385', '-0.4336', '-0.2603', '-0.1431', '0.78', '-0.1638', '-0.04266', '0.228', '-0.2957', '-0.04898', '-0.1898', '-0.1935', '0.448', '-0.413', '-0.1012', '-0.395', '0.1116', '0.2487', '-0.0926', '-0.06158', '0.0911', '0.01023', '-0.0275', '-0.2893', '0.2079', '-0.04694', '-0.04376', '-0.10974', '-0.2186', '0.2825', '0.401', '-0.10583', '-0.1127', '-0.02774', '-0.1671', '0.1611', '-0.4443', '-0.3022', '0.6357', '-0.1433', '-0.4626', '0.07855', '0.1026', '0.0982', '-0.0416', '-0.00862', '0.01534', '0.4263', '0.3618', '0.5337', '-0.01614', '0.4507', '-0.2493', '-0.2986', '0.3489', '0.4844', '0.28', '0.302', '-0.1915', '0.3816', '-0.01114', '-0.4683', '0.0967', '-0.3801', '0.4966', '0.2568', '-0.01932', '-0.376', '0.1094', '0.566', '0.1019', '0.1644', '0.08496', '0.337', '0.1732', '0.08875', '0.42', '-0.0913', '0.761', '-0.722', '0.0501', '-0.078']",C118435,0008878,C535729,,,,
mondo:0007485,"dyskeratosis congenita, autosomal dominant 1","['dyskeratosis congenita, Scoggins type', 'DKCA1', 'dyskeratosis congenita, autosomal dominant 1', 'autosomal dominant dyskeratosis congenita', 'dyskeratosis congenita, autosomal dominant type 1', 'autosomal dominant dyskeratosis congenita 1', 'dyskeratosis congenita Scoggins type', 'dyskeratosis congenita autosomal dominant', 'DKCA']",0070014,127550,,,,C176921,,C565079,,,,
mondo:0007486,hereditary benign intraepithelial dyskeratosis,"['Dkbi', 'dyskeratosis, hereditary benign intraepithelial', 'HBID', 'Witkop-Von Sallmann disease', 'hereditary benign corneal intraepithelial dyskeratosis']",,127600,352657,C0265966,,C3940,,C562551,,,,
mondo:0007487,"dyslexia, susceptibility to, 1","['dyslexia, susceptibility to, type 1', 'dyslexia, susceptibility to, 7', 'dyslexia, susceptibility to, 1', 'Word-blindness, congenital', 'dyslexia, susceptibility to, 4', 'susceptibility to dyslexia 1', 'DYX1', 'reading disability, specific, 1']",,127700,,,,,,,,,,
mondo:0007488,Lewy body dementia,"['dementia with Lewy bodies', 'diffuse Lewy body disease with gaze palsy', 'Lewy body disease', 'Lewy body variant of Alzheimer disease', 'diffuse Lewy body disease', 'Senile dementia of the Lewy body type', 'Lewy body dementia', 'dementia, Lewy body', 'DLB', 'lewy body dementia, susceptibility to', 'cortical Lewy body disease']",12217,127750,1648,C0752347,"['0.2588', '-0.1227', '-0.291', '-0.4785', '-0.3184', '-0.342', '0.0162', '0.1365', '-1.061', '-0.4094', '-0.07086', '-0.4824', '0.2358', '0.7437', '0.4614', '-0.7095', '-0.2576', '-0.3662', '-0.5244', '0.1418', '0.2428', '-0.1428', '-0.2058', '-0.03412', '0.773', '-0.3225', '-0.1361', '0.1396', '-0.218', '-0.1575', '0.3242', '-0.1495', '-0.1876', '-0.566', '0.8457', '-0.4126', '-0.4421', '-0.4294', '0.2795', '-1.158', '0.6484', '-0.603', '0.3037', '-0.0475', '0.1226', '-0.1753', '0.629', '-0.3828', '0.441', '0.376', '0.1643', '0.1164', '0.1396', '-0.55', '0.296', '0.2578', '0.1278', '-0.514', '-0.629', '-0.636', '-0.0787', '0.2173', '0.403', '-0.9785', '-0.005318', '0.8623', '0.2861', '1.037', '-0.7573', '0.869', '0.2205', '0.01521', '0.1153', '0.1926', '-0.4106', '1.03', '0.2852', '0.2041', '-0.963', '0.02669', '-0.275', '-0.74', '-0.4827', '1.029', '0.6846', '0.5044', '-0.2477', '-0.2296', '1.651', '0.817', '0.3042', '0.5283', '-0.3127', '0.798', '-0.5264', '0.3928', '-0.4707', '-0.205', '-0.6733', '-0.423']",C84826,0006792,,331.82,G31.83,,
mondo:0007489,dysplasia epiphysealis hemimelica,"['dysplasia epiphysealis hemimelica', 'Trevor disease']",,127800,1822,C0432282,,,,C537997,756.59,,,
mondo:0007490,carpotarsal osteochondromatosis,"['Maroteaux Le Merrer Bensahel syndrome', 'dominant carpotarsal osteochondromatosis', 'osteochondromatosis, dominant carpotarsal', 'dysplasia epiphysealis hemimelica with CHONDROMAS and osteochondromas', 'Maroteaux-Le Merrer-Bensahel syndrome']",,127820,2767,C1300233,,,,C565076,,,,
mondo:0007491,dystelephalangy,"['Kirner deformity', 'congenital bilateral metadiaphyseal acrodysplasia of the little finger', 'dystelephalangy']",,128000,,C1851955,,,,C538000,,,,
mondo:0007492,early-onset generalized limb-onset dystonia,"['dystonia musculorum deformans', 'early-onset generalised torsion dystonia', 'EOTD', 'idiopathic dystonia DYT1', 'Oppenheim dystonia', 'Oppenheim^s dystonia', 'early-onset generalized torsion dystonia', 'Primary torsion dystonia', 'torsion dystonia 1', 'DYT-TOR1A', 'DYT-TOR1A dystonia', 'early-onset generalized limb-onset dystonia', 'idiopathic torsion dystonia', 'Early-onset torsion dystonia', 'Early-onset Primary dystonia', 'early-onset torsion dystonia', 'torsion dystonia 1, autosomal dominant', 'early-onset primary dystonia', 'early onset primary dystonia', 'dystonia 1, torsion, autosomal dominant', 'dystonia-1, torsion', 'dystonia musculorum deformans 1', 'early onset torsion dystonia', 'dystonia 1', 'idiopathic dystonia', 'Dyt1', 'DYT1', 'torsion dystonia type 1', 'dystonia 1, torsion, Autosomal dominant']",0060730,128100,256,C3888090,"['0.6416', '0.2443', '-0.3667', '-0.2625', '-0.2507', '-1.116', '0.736', '0.1442', '-0.583', '-0.12115', '0.583', '0.8135', '-0.1644', '0.4814', '0.4785', '0.517', '-0.0842', '-0.8037', '-0.416', '-0.8784', '-0.5327', '-0.2788', '0.3164', '-0.2334', '-0.616', '0.1847', '0.1616', '0.2053', '-0.1702', '0.1742', '0.517', '0.1461', '0.5303', '-0.05865', '0.656', '-0.2203', '0.6504', '-0.619', '0.3655', '-0.2263', '0.2458', '-0.2465', '-0.2646', '-0.1343', '0.8833', '0.2335', '-0.3704', '0.043', '0.0997', '0.4304', '0.1956', '0.1498', '0.385', '-0.661', '0.3794', '0.0445', '0.2328', '0.445', '0.1012', '-0.519', '-0.3293', '-0.508', '-0.3103', '-0.6846', '-0.964', '0.742', '0.307', '-0.3604', '-0.2268', '0.2141', '-0.392', '-0.532', '-0.09875', '-0.11945', '0.2715', '0.611', '0.8804', '-0.173', '-0.171', '-0.433', '-0.1456', '0.1125', '0.5493', '0.539', '0.521', '-0.0312', '0.0948', '0.3696', '1.443', '0.03305', '0.1292', '0.0838', '0.1902', '0.01892', '0.9883', '-0.2296', '-0.2203', '-0.02339', '0.5127', '-0.613']",C116718,,C538005,,,,
mondo:0007493,torsion dystonia 4,"['whispering dysphonia', 'hereditary whispering dysphonia', 'torsion dystonia type 4', 'dystonia musculorum deformans 4', 'DYT4', 'dystonia 4, torsion, autosomal dominant', 'autosomal dominant torsion dystonia-4', 'whispering dysphonia, hereditary', 'primary dystonia, DYT4 type']",0090041,128101,98805,C1860315,"['0.7305', '0.2642', '-0.1703', '-0.1888', '0.06155', '-1.355', '0.613', '0.0735', '-0.5986', '-0.015495', '0.92', '0.852', '-0.3877', '0.4482', '0.687', '0.6772', '0.0872', '-0.456', '-0.779', '-1.084', '-0.4456', '0.06665', '-0.2627', '-0.3442', '-0.3335', '0.2206', '-0.2156', '0.1031', '0.001852', '-0.05298', '0.698', '0.459', '0.7666', '-0.1575', '0.7446', '-0.2269', '0.541', '-0.2207', '0.512', '-0.5186', '0.5625', '-0.03387', '-0.5713', '-0.01848', '0.3584', '-0.013535', '-0.347', '0.04474', '0.2317', '0.0654', '0.3357', '0.12213', '0.486', '-0.1764', '0.676', '-0.1384', '0.0293', '0.8784', '0.1475', '-0.2003', '-0.6455', '-0.3005', '-0.03275', '-0.6914', '-0.8823', '0.524', '0.374', '0.4705', '-0.2009', '0.3389', '-0.3914', '-0.211', '-0.0641', '-0.03668', '0.3994', '0.6816', '0.7754', '0.1462', '-0.063', '-0.4067', '-0.2201', '0.3806', '0.436', '0.5176', '0.9707', '0.1584', '0.264', '0.7183', '1.625', '-0.05057', '0.4404', '0.167', '0.704', '0.3088', '1.326', '-0.1284', '-0.247', '0.2172', '0.3872', '-0.4067']",,,,,,,
mondo:0007495,dystonia 5,"['Segawa syndrome, autosomal dominant', 'hereditary progressive dystonia with marked diurnal fluctuation', 'dystonia 5', 'autosomal dominant Segawa syndrome', 'dystonia type 5', 'GTPCH1-deficient dopa-responsive dystonia', 'Dopa-responsive dystonia, autosomal dominant', 'dystonia-Parkinsonism with diurnal fluctuation', 'dystonia, DOPA-responsive, with or without hyperphenylalaninemia', 'DYT-GCH1', 'HPD with marked diurnal fluctuation', 'GTPCH1-deficient DRD', 'GTP cyclohydrolase 1-deficient dopa-responsive dystonia', 'DRD', 'autosomal dominant dopa-responsive dystonia', 'DYT5a', 'dystonia, DOPA-responsive', 'dystonia, progressive, with diurnal variation', 'Dopa-responsive dystonia; Segawa syndrome AD', 'dystonia, Dopa-responsive, autosomal dominant']",0090043,128230,98808,CN207122,"['0.5605', '0.1804', '-0.3955', '-0.3884', '-0.02797', '-0.7715', '0.427', '0.675', '-0.4739', '-0.27', '0.6445', '0.725', '-0.2412', '0.6333', '0.557', '0.543', '-0.1263', '-0.6763', '-0.471', '-0.5693', '-0.5645', '-0.3748', '0.3572', '0.1727', '-0.2507', '0.3809', '0.1964', '-0.1271', '-0.1892', '0.016', '0.1166', '0.3123', '0.4182', '0.1225', '-0.02397', '0.11816', '0.5435', '0.05493', '0.2603', '-0.4565', '0.3035', '-0.2666', '-0.05673', '-0.02213', '0.6016', '-0.3022', '-0.649', '0.342', '-0.3337', '0.552', '0.05466', '0.0727', '0.3555', '-0.2627', '0.6904', '0.01607', '0.31', '0.002295', '0.2783', '-0.1451', '-0.4565', '-0.09735', '-0.1002', '-0.534', '-1.025', '0.689', '0.3047', '-0.0904', '-0.526', '0.2384', '0.0941', '-0.3132', '0.1131', '-0.10016', '0.4353', '0.4036', '0.4158', '-0.512', '0.2219', '-0.1238', '-0.3254', '-0.1292', '0.9688', '0.47', '1.027', '0.4382', '0.06116', '0.0477', '1.259', '0.3596', '0.1387', '-0.0825', '-0.0296', '0.1678', '0.7075', '0.09845', '-0.1838', '-0.1316', '0.4883', '-0.23']",,,,,,,
mondo:0007496,dystonia 12,"['DYT-ATP1A3', 'DYT12', 'RDP', 'dystonia 12', 'rapid-onset dystonia-parkinsonism', 'ATP1A3 dystonic disorder', 'dystonia-Parkinsonism, rapid-onset', 'dystonia type 12', 'dystonia-12', 'dystonic disorder caused by mutation in ATP1A3']",0090056,128235,71517,C1868681,"['0.6143', '0.2576', '-0.61', '-0.1721', '-0.3308', '-0.9653', '0.584', '0.3708', '-0.5425', '-0.3403', '0.6006', '0.6924', '-0.014175', '0.531', '0.4353', '0.5444', '-0.2185', '-0.9404', '-0.4773', '-0.7197', '-0.39', '-0.074', '-0.2327', '-0.366', '-0.2734', '0.0866', '-0.1644', '0.11206', '-0.3086', '-0.01519', '0.2783', '0.605', '0.535', '-0.00851', '0.3833', '-0.1869', '0.3628', '-0.0832', '0.04456', '0.05765', '0.3884', '-0.579', '-0.0766', '0.0284', '0.6016', '-0.0917', '-0.4404', '0.1754', '0.3599', '0.2756', '0.1614', '-0.05518', '0.393', '0.1667', '0.701', '0.09406', '0.193', '0.4521', '0.179', '-0.1442', '-0.3408', '-0.11597', '0.1235', '-0.866', '-0.774', '0.504', '0.1917', '0.2837', '-0.1471', '0.53', '-0.3088', '-0.12366', '-0.266', '-0.2466', '0.4155', '0.9326', '0.6567', '-0.3223', '0.3438', '0.0771', '0.02774', '-0.0417', '0.61', '0.4712', '0.8687', '0.532', '0.2039', '0.1426', '1.559', '0.1862', '0.6606', '0.06183', '0.2927', '0.1459', '0.7544', '-0.1032', '-0.1019', '0.05856', '0.4822', '-0.128']",C157577,,C538001,,,,
mondo:0007497,"ear antitragus, tag at base of","['ear antitragus, tag at base of']",,128290,,,,,,,,,,
mondo:0007498,ear exostoses,"['ear exostoses', 'exostoses of external auditory canal']",,128300,,C0155411,,,,,,,,
mondo:0007499,ear folding,['ear folding'],,128500,,,,,,,,,,
mondo:0007500,ear malformation,"['cup Ear', 'ear malformation']",,128600,,,,,,,744.3,,,
mondo:0007501,"preauricular fistulae, congenital","['Pafc', 'preauricular fistulae, congenital', 'Ear pits']",,128700,,,,,,C563015,,,,
mondo:0007502,"ear pits, posterior helical","['posterior helical Ear pits', 'earlobe Indentations, posterior', 'ear pits, posterior helical']",,128710,,,,,,,,,,
mondo:0007503,ear without helix,['ear without helix'],,128800,,,,,,,,,,
mondo:0007504,thickened earlobes-conductive deafness syndrome,"['Escher-Hirt syndrome', 'Escher Hirt syndrome', 'earlobes, thickened, with conductive deafness from incudostapedial abnormalities']",,128980,2405,,,,,,,,,
mondo:0007505,"earring holes, natural","['earlobe sinuses', 'earring holes, natural']",,129000,,,,,,,,,,
mondo:0007507,absence of fingerprints-congenital milia syndrome,"['ectodermal dysplasia, absent dermatoglyphic pattern, changes in nails, and Simian Crease', 'absence of fingerprints congenital milia', 'adermatoglyphia with congenital facial milia and acral blisters, digital contractures, and nail abnormalities', 'absence of dermatoglyphics congenital milia', 'Baird syndrome', 'absence of dermatoglyphics-congenital milia syndrome', 'Basan syndrome']",0080725,129200,1658,,"['-0.0847', '-0.02519', '-0.4736', '0.02612', '0.2299', '-0.7646', '-0.5493', '0.3818', '-0.383', '-0.4878', '-0.2173', '-0.284', '-0.176', '-0.0649', '-0.204', '0.586', '0.3726', '-0.2727', '-0.1775', '-0.3762', '-0.3513', '0.10645', '0.537', '-0.1792', '0.531', '0.273', '-0.5815', '0.3186', '0.05786', '-0.4924', '0.4368', '-0.851', '-0.1464', '0.0809', '-0.2156', '-0.1421', '-0.06067', '-0.6133', '0.0348', '-0.319', '-0.01744', '-0.6875', '-0.1705', '-0.1992', '-0.0892', '-0.2546', '-0.3186', '0.5693', '-0.1376', '-0.44', '-0.3047', '-0.2468', '0.412', '0.1979', '-0.495', '-0.4185', '0.713', '0.325', '-0.705', '0.02646', '-0.3154', '-0.1528', '-0.12354', '0.38', '-0.353', '-0.02267', '0.04904', '0.2487', '-0.0798', '0.2384', '-0.11554', '0.02289', '0.2847', '0.0958', '0.1924', '0.05045', '-0.1071', '-0.06033', '-0.2404', '-0.05423', '-0.2136', '0.3403', '0.783', '-0.1053', '0.202', '-0.0799', '-0.135', '0.78', '0.1304', '-0.3801', '-0.2686', '0.6875', '0.4998', '-0.1114', '0.6606', '0.4368', '0.2852', '-0.829', '0.417', '-0.1832']",,,C537659,,,,
mondo:0007508,Rapp-Hodgkin syndrome,"['Rapp-Hodgkin ectodermal dysplasia syndrome', 'anhidrotic ectodermal dysplasia with cleft lip/palate', 'cleft lip with or without cleft palate, nonsyndromic, 8', 'ectodermal dysplasia, anhidrotic, with cleft Lip/palate', 'Rapp-Hodgkin syndrome', 'orofacial cleft 8', 'RHS', 'ectodermal dysplasia, anhidrotic, with cleft lip-palate', 'OFC8, included']",0060330,129400,3022,CN203427,,,,C535289,,,,
mondo:0007509,"ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant","['hypohidrotic ectodermal dysplasia autosomal dominant', 'ectodermal dysplasia, hypohidrotic, autosomal dominant', 'ectodermal dysplasia hypohidrotic autosomal dominant', 'ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant', 'ECTD10A']",0111663,129490,,C3888065,,,,,,,,
mondo:0007510,Clouston syndrome,"['Clouston^s syndrome', 'alopecia, dysplastic nails, palmar and plantar hyperkeratosis', 'ectodermal dysplasia, hidrotic, 2', 'autosomal dominant hidrotic ectodermal dysplasia', 'hidrotic ectodermal dysplasia, autosomal dominant', 'Clouston^s hidrotic ectodermal dysplasia', 'ectodermal dysplasia 2, Clouston type', 'ectodermal dysplasia, hidrotic, 2, formerly', 'palmoplantar hyperkeratosis and alopecia', 'hidrotic ectodermal dysplasia', 'ED2', 'Clouston syndrome', 'ectodermal dysplasia, hidrotic, autosomal dominant', 'Patel Bixler syndrome', 'hidrotic ectodermal dysplasia syndrome', 'Clouston hidrotic ectodermal dysplasia', 'ectodermal dysplasia, hidrotic']",14693,129500,189,,"['-0.05032', '0.3496', '-0.1043', '0.1737', '0.2778', '-0.4106', '-0.1885', '0.8906', '0.0063', '-0.4575', '-0.254', '0.1609', '-0.771', '0.2566', '0.3535', '0.4448', '0.623', '-0.4434', '-0.6084', '-0.9023', '-0.3408', '-0.2206', '0.6094', '-0.1046', '0.2429', '0.2146', '-0.3337', '0.1963', '-0.1178', '-0.05667', '0.5137', '-0.165', '-0.541', '0.3923', '0.2659', '-0.01915', '-0.04398', '-0.1339', '0.1298', '0.1702', '0.03653', '0.1252', '-0.2067', '-0.197', '0.5137', '-0.01169', '-0.221', '-0.1017', '-0.02206', '-0.4924', '0.2001', '-0.1517', '0.6255', '0.0636', '0.04703', '-0.03035', '0.2822', '-0.09357', '-0.2395', '-0.187', '0.02704', '0.0852', '-0.1649', '-0.3406', '0.1678', '0.255', '0.3154', '0.33', '-0.00726', '0.7397', '-0.2732', '-0.3052', '0.1595', '0.06555', '-0.11255', '-0.3022', '0.0585', '0.0542', '0.1913', '-0.4275', '0.2935', '-0.0654', '0.2128', '0.3748', '0.1406', '0.10394', '-0.001621', '-0.02304', '0.7505', '0.593', '0.2137', '0.32', '0.2952', '0.3818', '0.5845', '0.00884', '0.4995', '-0.1158', '0.4932', '-0.1835']",,,,,,,
mondo:0007511,"ectodermal dysplasia, trichoodontoonychial type","['ectodermal dysplasia trichoodontoonychial type', 'ectodermal dysplasia, trichoodontoonychial type']",,129510,1818,C1851858,,,,C565068,,,,
mondo:0007512,ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet,['ectodermal dysplasia syndrome with distinctive facial appearance and preaxial polydactyly of feet'],,129540,,C1851851,,,,C565067,,,,
mondo:0007513,ectodermal dysplasia with adrenal cyst,"['Odonto-onycho-hypohidrotic dysplasia-midline scalp defects syndrome', 'ectodermal dysplasia with adrenal cyst']",,129550,3391,C1851850,,,,C538015,,,,
mondo:0007514,"ectopia lentis 1, isolated, autosomal dominant","['ECTOL1', 'ectopia lentis 1, isolated, autosomal dominant', 'isolated ectopia lentis caused by mutation in FBN1', 'ectopia lentis, familial', 'autosomal dominant isolated ectopia lentis 1', 'FBN1 isolated ectopia lentis']",0111150,129600,,C3541518,,,,,,,,
mondo:0007515,ectopia pupillae,"['familial ectopic pupil', 'ectopia pupillae (disease)', 'ectopia pupillae', 'congenital eye malformation in which the pupils are displaced from their normal central position']",,129750,,,,,,C536185,,,,0009918
mondo:0007516,ectrodactyly and ectodermal dysplasia without cleft lip/palate,"['ectrodactyly-ectodermal dysplasia without clefting syndrome', 'EEC syndrome without cleft Lip/palate', 'ectrodactyly and ectodermal dysplasia without cleft lip/palate']",,129810,1888,C1851849,,,,C565065,,,,
mondo:0007517,ectrodactyly-cleft palate syndrome,"['ectrodactyly-cleft palate syndrome', 'Ecp syndrome']",,129830,1889,CN229012,,,,C565064,,,,
mondo:0007518,"edema, familial idiopathic, prepubertal","['edema, familial idiopathic, prepubertal']",,129840,,C1851847,,,,C565063,,,,
mondo:0007519,Edinburgh malformation syndrome,"['typus Edinburgensis', 'Edinburgh malformation syndrome']",,129850,1895,C0795933,,,,C563051,,,,
mondo:0007520,"ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1","['EEC1', 'ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome type 1', 'ectrodactyly, ectodermal dysplasia, and cleft LIP/palate syndrome 1', 'EEC syndrome-1', 'EEC', 'EEC syndrome 1']",0060784,129900,,,,,,C565062,,,,
mondo:0007522,"Ehlers-Danlos syndrome, classic type","['Ehlers-Danlos syndrome, classic type', 'classic Ehlers-Danlos syndrome', 'classical Ehlers-Danlos syndrome', 'EDS II', 'Ehlers Danlos syndrome, mild classic type, formerly', 'Ehlers-Danlos syndrome, type II, formerly', 'Ehlers-Danlos syndrome, gravis type', 'Ehlers Danlos syndrome, mitis type', 'EDS, classic type', 'EDS I, formerly', 'Ehlers-Danlos syndrome type 2', 'Ehlers Danlos syndrome, mild classic type', 'Ehlers-Danlos syndrome, type I', 'Ehlers-Danlos syndrome, gravis type, formerly', 'EDS II, formerly', 'Ehlers-Danlos syndrome, severe classic type, formerly', 'Ehlers-Danlos syndrome type 2 (formerly)', 'Ehlers Danlos syndrome, mitis type, formerly', 'Ehlers-Danlos syndrome, type II', 'Ehlers-Danlos syndrome type 1 (formerly)', 'Ehlers-Danlos syndrome, severe classic type', 'EDS I', 'Ehlers-Danlos syndrome, type I, formerly']",,,287,C4225429,"['0.3818', '0.004753', '-0.626', '-0.1982', '0.4268', '-0.4746', '0.4062', '0.7417', '-0.687', '0.8105', '-0.1897', '-0.267', '0.07196', '1.184', '-0.5923', '0.5137', '-0.7124', '0.0786', '-0.10126', '-0.504', '0.2397', '0.4404', '0.289', '0.1318', '-0.5767', '0.2053', '0.605', '0.10345', '1.332', '0.227', '0.9907', '-0.2101', '0.1594', '-0.06464', '-0.1345', '0.2213', '-0.3457', '-0.05865', '0.0948', '-0.585', '0.576', '-0.08386', '-0.717', '0.03775', '0.09357', '-0.2856', '-0.4902', '0.622', '0.4788', '0.02814', '-0.2032', '-0.8335', '0.561', '0.02057', '0.005104', '-0.2048', '-0.2727', '0.8306', '0.4824', '0.1722', '0.02277', '0.605', '0.165', '0.1105', '0.1263', '0.3765', '-0.08215', '0.8535', '-0.05887', '1.079', '-0.8525', '0.10187', '-0.4375', '-0.1573', '-0.2051', '-0.2996', '-0.2432', '-0.0968', '-0.2078', '-0.4312', '-0.2227', '-0.3186', '0.0809', '0.224', '-0.736', '0.2131', '-0.02908', '0.597', '0.364', '-0.431', '0.7876', '0.377', '-0.264', '0.3367', '0.308', '0.1754', '1.011', '-0.0002532', '0.473', '0.1609']",,,,,,,
mondo:0007523,"Ehlers-Danlos syndrome, hypermobility type","['Ehlers-Danlos syndrome, type III', 'HT-EDS', 'benign hypermobility syndrome', 'EDSHMB', 'EDS 3', 'hypermobile Ehlers-Danlos syndrome', 'Ehlers-Danlos syndrome, hypermobility type', 'benign joint hypermobility syndrome', 'EDS3 (formerly)', 'Ehlers-Danlos syndrome type 3', 'hypermobile EDS', 'BJHS', 'Ehlers-Danlos syndrome, type 3', 'Ehlers-Danlos syndrome type 3 (formerly)', 'hEDS', 'Ehlers-Danlos syndrome, hypermobile type', 'EDS III']",14757,130020,285,C0268337,,C125698,,C536196,,,,
mondo:0007524,"autosomal dominant Ehlers-Danlos syndrome, vascular type","['autosomal dominant type IV Ehlers-Danlos syndrome', 'Ehlers-Danlos syndrome, vascular type', 'EDSVASC', 'Ehlers-Danlos syndrome, vascular type, autosomal dominant', 'Ehlers-Danlos syndrome, sack-Barabas type', 'Ehlers-Danlos syndrome, Ecchymotic type', 'Ehlers-Danlos syndrome, arterial type', 'EDS 4', 'Ehlers-Danlos syndrome, type IV, autosomal dominant']",14756,130050,,,,,,,,,,
mondo:0007525,"Ehlers-Danlos syndrome, arthrochalasis type","['Ehlers-Danlos syndrome, type VII', 'Ehlers-Danlos syndrome, type VII, autosomal dominant', 'EDS VII', 'Ehlers-Danlos syndrome, arthrochalasia type', 'arthrochalasia EDS', 'Ehlers-Danlos syndrome type 7', 'EDS 7A', 'EDS 7B', 'arthrochalasia Ehlers-Danlos syndrome', 'EDS VII, mutant procollagen type', 'EDSARTH1', 'AEDS', 'Ehlers-Danlos syndrome type 7A (formerly)', 'EDS7A (formerly)', 'Ehlers-Danlos syndrome, arthrochalasia type, 1', 'Ehlers-Danlos syndrome, type VIIA, autosomal dominant', 'arthrochalasis multiplex congenita']",0080727,130060,1899,CN200649,"['0.508', '-0.175', '-0.10223', '0.0623', '0.1156', '-0.6104', '-0.08826', '1.225', '-0.868', '0.3022', '0.04077', '-0.2441', '0.4368', '1.007', '-0.2498', '0.3606', '-0.52', '0.1536', '-0.1365', '-0.7227', '-0.02', '0.448', '0.149', '0.10815', '-0.0765', '0.389', '0.2588', '0.2375', '1.089', '0.4653', '0.6577', '-0.5303', '-0.04794', '0.1134', '0.136', '-0.2878', '-0.06744', '-0.3157', '0.1412', '-0.7427', '0.583', '-0.3037', '-0.6523', '0.361', '0.1259', '0.0826', '-0.61', '0.671', '0.872', '-0.4868', '0.2135', '-0.8154', '0.522', '-0.02934', '0.486', '-0.5684', '-0.3215', '0.3218', '0.3625', '-0.0671', '-0.2465', '0.2186', '-0.02156', '-0.3645', '-0.09204', '0.2673', '-0.0689', '0.6895', '-0.1884', '0.806', '-0.3384', '-0.2817', '-0.2827', '-0.1329', '-0.10583', '-0.2825', '-0.1029', '-0.2622', '0.1235', '0.04825', '-0.3867', '-0.543', '0.3352', '1.046', '-0.7026', '0.299', '-0.1704', '0.7856', '0.0498', '0.1197', '0.0563', '0.4614', '-0.3843', '-0.1644', '0.4504', '0.01219', '0.592', '-0.475', '0.64', '-0.1959']",C125701,,C562625,,,,
mondo:0007526,"Ehlers-Danlos syndrome, spondylodysplastic type","['Ehlers-Danlos syndrome progeroid type', 'dermatan sulphate proteoglycan', 'B4GALT7-CDG', 'proteodermatan sulfate, defective biosynthesis of', 'EDSSPD1', 'Ehlers-Danlos syndrome with short stature and limb anomalies', 'Pds, defective biosynthesis of', 'EDS, progeroid type', 'Ehlers-Danlos syndrome, progeroid type', 'defective biosynthesis of proteodermatan sulfate', 'xylosylprotein 4-beta-galactosyltransferase deficiency', 'Ehlers-Danlos syndrome, spondylodysplastic type, 1', 'XGPT deficiency', 'galactosyltransferase 1 deficiency', 'galactosyltransferase I deficiency', 'Ehlers-Danlos syndrome, progeroid type (former)', 'PDS', 'spondylodysplastic Ehlers-Danlos syndrome', 'defective biosynthesis of proteodermatan sulphate', 'dermatan sulfate proteoglycan']",0050802,,75496,C1869122,"['0.3987', '-0.02142', '-0.2211', '0.2213', '0.3992', '-0.4092', '-0.2118', '0.67', '-0.711', '0.3447', '-0.04416', '-0.5005', '0.3142', '0.9907', '-0.545', '0.2153', '-0.4475', '0.03555', '0.2413', '-0.6006', '0.2273', '0.781', '0.1071', '0.01433', '-0.11066', '0.3823', '-0.02539', '0.3723', '1.53', '0.139', '0.8545', '-0.652', '0.12177', '-0.0177', '0.2654', '0.25', '-0.2002', '-0.4358', '0.1674', '-0.752', '0.5557', '-0.1007', '-0.679', '0.3188', '0.487', '-0.399', '-0.3486', '0.891', '0.5864', '-0.4585', '0.132', '-0.4038', '0.616', '-0.1323', '-0.06726', '-0.5483', '-0.6626', '0.4026', '0.2668', '-0.1593', '0.127', '0.3052', '0.1823', '-0.00633', '-0.01744', '0.1464', '-0.408', '1.089', '-0.1437', '0.78', '-0.447', '0.2668', '-0.4424', '-0.3623', '-0.11633', '-0.3362', '-0.3723', '-0.1276', '-0.1088', '-0.1666', '0.02509', '-0.3167', '0.375', '0.746', '-0.9214', '0.01671', '-0.0697', '0.7153', '0.3318', '-0.06055', '0.316', '0.546', '-0.5464', '0.2175', '0.588', '0.1289', '0.621', '-0.1443', '0.685', '-0.1344']",,,C536201,,,,
mondo:0007527,"Ehlers-Danlos syndrome, periodontitis type","['pEDS', 'Ehlers-Danlos syndrome, type 8', 'EDS VIII', 'EDS8', 'Ehlers-Danlos syndrome, periodontosis type', 'Ehlers-Danlos syndrome, type VIII', 'periodontal EDS', 'EDS 8', 'Ehlers-Danlos syndrome, periodontitis type', 'Ehlers-Danlos syndrome type 8', 'EDS VIII (formerly)', 'EDS8 (formerly)', 'Ehlers-Danlos syndrome, type VIII (formerly)', 'Ehlers-Danlos syndrome type 8 (formerly)', 'periodontal Ehlers-Danlos syndrome']",,,75392,,"['0.989', '-0.3074', '0.17', '0.6797', '0.4375', '-0.57', '0.2041', '0.224', '-0.4204', '0.895', '-0.29', '-0.478', '-0.1566', '0.772', '-0.3052', '-0.0629', '-0.536', '0.9336', '-0.3489', '-1.025', '-0.03226', '-0.3748', '0.1663', '-0.2257', '-0.28', '-0.147', '-0.787', '-0.0643', '0.1174', '-0.381', '-0.1105', '0.4932', '-0.12415', '0.7793', '0.9287', '0.7856', '-0.07184', '0.0677', '0.4783', '-0.6562', '0.1693', '-0.04022', '-0.7676', '-0.2306', '0.2157', '0.0644', '-0.1184', '0.02956', '-0.01924', '-0.3657', '-0.1451', '-0.05212', '0.763', '0.003544', '-0.1907', '-0.4602', '-0.7104', '0.02957', '-1.128', '-0.614', '0.01836', '0.171', '-0.3264', '-0.5366', '0.01305', '-0.10785', '0.516', '0.01025', '0.3232', '1.042', '-0.04837', '-0.1844', '0.5127', '-0.892', '0.821', '0.1018', '0.2158', '0.4014', '-0.141', '-0.6055', '-0.724', '-0.639', '-0.001145', '0.03598', '0.3267', '0.02242', '0.1316', '-0.1103', '0.2852', '-0.1597', '0.5786', '0.5557', '0.1937', '0.566', '0.09247', '0.02109', '0.05975', '-0.6733', '-0.03598', '-0.06003']",,,C562626,,,,
mondo:0007528,"Ehlers-Danlos syndrome, autosomal dominant, type unspecified","['Ehlers-Danlos syndrome, Friedman-Harrod type', 'Ehlers-Danlos syndrome, autosomal dominant, type unspecified', 'EDS, unspecified type']",,130090,,C0220679,,,,C562424,,,,
mondo:0007529,elastosis perforans serpiginosa,"['elastoma Intrapapillare perforans verruciformis', 'elastosis perforans serpiginosa', 'Miescher elastoma', 'eps']",,130100,79148,C0221271,,,,C536202,,L87.2,10014338,
mondo:0007530,electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon,['electroencephalographic peculiarity: 14 and 6 per sec. positive spike phenomenon'],,130200,,,,,,,,,,
mondo:0007531,electroencephalographic peculiarity: fronto-precentral beta wave groups,['electroencephalographic peculiarity: fronto-precentral beta wave groups'],,130300,,,,,,,,,,
mondo:0007533,elliptocytosis 2,"['elliptocytosis-2', 'SPTA1 hereditary elliptocytosis', 'EL2', 'hereditary elliptocytosis caused by mutation in SPTA1', 'elliptocytosis 2', 'elliptocytosis, Rhesus-unlinked type', 'elliptocytosis type 2']",,130600,,C1851741,,,,C565058,,,,
mondo:0007534,Beckwith-Wiedemann syndrome,"['EMG syndrome', 'Wiedemann-Beckwith syndrome (WBS)', 'exomphalos macroglossia gigantism syndrome', 'BWS', 'Beckwith-Wiedemann syndrome', 'exomphalos-macroglossia-gigantism syndrome', 'Beckwith-Wiedemann syndrome chromosome region', 'Wiedemann-Beckwith syndrome']",5572,130650,116,C0004903,"['-0.4602', '0.6377', '0.0527', '-0.01082', '-0.005226', '-0.3364', '0.6016', '0.7065', '-0.8247', '-0.382', '-0.0369', '0.2316', '0.586', '0.02875', '-0.2086', '0.376', '0.1024', '-0.4822', '-0.476', '-0.1793', '0.06866', '0.144', '0.5264', '-0.1438', '0.1603', '0.2278', '0.04022', '0.2668', '0.5537', '-0.4329', '0.4495', '0.07416', '0.5635', '-0.1521', '-0.2942', '0.2023', '0.03387', '-0.1293', '-0.6597', '-0.2837', '-0.1605', '0.3853', '0.283', '0.11676', '0.5093', '-0.3682', '0.08984', '-0.2883', '-0.0691', '0.2427', '-0.0793', '0.341', '-0.5303', '-0.218', '-0.3044', '-0.1411', '0.2429', '0.2083', '-0.4062', '0.9194', '0.3044', '-0.10535', '-0.1729', '-0.0844', '0.005672', '0.1421', '0.46', '0.1456', '-0.05716', '0.8896', '0.449', '0.51', '-0.0577', '0.4348', '-0.262', '-0.7583', '0.3625', '0.1575', '-0.669', '-0.03745', '-0.373', '0.484', '-0.1698', '-0.1646', '-0.3018', '0.1499', '0.5664', '0.3335', '0.4023', '-0.1071', '-0.1018', '0.04828', '-0.3757', '-0.482', '1.081', '-0.3682', '0.3716', '-0.2778', '0.005867', '0.0608']",C34415,,D001506,759.89,,10050344,
mondo:0007535,"emphysema, hereditary pulmonary","['emphysema, hereditary pulmonary']",,130700,,C1851718,,,,C565057,,,,
mondo:0007536,congenital lobar emphysema,"['emphysema, congenital lobar', 'CLE', 'infantile lobar hyperinflation', 'congenital lobar hyperinflation']",,130710,1928,C0265797,,C98895,,C535735,,,10010456,
mondo:0007537,lateral meningocele syndrome,"['Lms', 'Lehman syndrome', 'LMNS', 'lateral meningocele syndrome']",0111343,130720,2789,C1851710,"['-0.1388', '0.03003', '0.4565', '-0.3591', '0.0807', '-0.1757', '0.16', '0.3909', '-0.4412', '0.03973', '0.09814', '-0.095', '-0.05182', '-0.1672', '-0.2167', '0.01628', '0.1798', '-0.1425', '-0.2368', '-0.3394', '0.1978', '0.0849', '0.3516', '-0.03078', '0.248', '-0.0258', '-0.3162', '-0.0806', '0.3171', '-0.2898', '0.2776', '-0.186', '0.4158', '0.337', '0.3145', '-0.3518', '-0.1868', '-0.2471', '-0.03568', '-0.554', '0.1241', '-0.11194', '-0.0644', '-0.05853', '0.0647', '-0.414', '0.2197', '0.4934', '-0.1361', '-0.02698', '-0.2054', '0.08887', '0.04724', '-0.00488', '-0.2566', '-0.2717', '-0.2052', '-0.075', '-0.1862', '0.1434', '0.3643', '0.004868', '-0.5996', '0.1897', '-0.111', '-0.1327', '0.2201', '0.2734', '-0.2064', '0.2864', '-0.3862', '0.118', '-0.06137', '-0.2312', '-0.2471', '-0.10394', '0.11804', '-0.06635', '-0.2644', '-0.1421', '0.04257', '-0.2064', '-0.08374', '0.6284', '-0.2742', '0.1484', '-0.206', '0.168', '0.1797', '0.2081', '0.03026', '0.322', '0.2751', '0.0965', '0.61', '0.03906', '0.5645', '-0.2045', '0.2072', '0.268']",,,C537878,,,,
mondo:0007538,"amelogenesis imperfecta, type 3A","['amelogenesis imperfecta, type IIIA', 'amelogenesis imperfecta hypomineralization type', 'AI3', 'ADHCAI', 'AI3A', 'amelogenesis imperfecta type 3', 'amelogenesis imperfecta type III', 'amelogenesis imperfecta, type 3A', 'autosomal dominant amelogenesis imperfecta hypocalcification type', 'amelogenesis imperfecta, type III', 'amelogenesis imperfecta, hypocalcification type, autosomal dominant', 'FAM83H amelogenesis imperfecta', 'amelogenesis imperfecta, hypomineralization type', 'amelogenesis imperfecta, type 3', 'amelogenesis imperfecta type 3A', 'amelogenesis imperfecta caused by mutation in FAM83H']",0110055,130900,100032,,"['-0.105', '0.1559', '0.10443', '-0.03096', '0.1229', '-0.2032', '-0.02058', '0.2086', '-0.2057', '-0.1361', '-0.1168', '-0.0751', '-0.1497', '-0.0593', '0.1425', '-0.1617', '0.02151', '-0.1001', '-0.05545', '-0.2983', '0.1002', '-0.04077', '0.2092', '-0.03604', '0.1082', '0.1257', '-0.07227', '0.02081', '0.01372', '-0.04648', '-0.07513', '0.08093', '0.0986', '0.1226', '0.253', '-0.0951', '0.03394', '-0.197', '-0.06067', '-0.2747', '0.0248', '-0.23', '0.0806', '-0.1134', '-0.1731', '-0.1433', '0.074', '0.1796', '0.218', '0.01029', '0.1573', '-0.168', '0.175', '-0.02107', '-0.1271', '-0.2175', '0.2944', '-0.1089', '-0.1466', '0.094', '0.11554', '0.10284', '0.0814', '-0.1103', '0.04016', '0.1088', '0.1348', '0.1', '-0.135', '0.1255', '-0.2203', '0.001706', '0.0484', '-0.254', '0.1428', '0.006973', '0.006817', '0.01936', '-0.11993', '-0.0636', '-0.02481', '0.03357', '-0.09625', '0.1594', '-0.0867', '-0.1222', '0.0496', '0.2245', '0.3086', '0.06088', '-0.01288', '0.0637', '0.0399', '0.04666', '0.3599', '0.074', '0.2268', '-0.2744', '0.11786', '-0.03452']",,,C562880,,,,
mondo:0007539,"encephalopathy, recurrent, of childhood","['Neuhauser Eichner Opitz syndrome', 'encephalopathy, recurrent, of childhood', 'encephalopathy recurrent of childhood']",,130950,2672,,,,,C536407,,,,
mondo:0007540,multiple endocrine neoplasia type 1,"['endocrine adenomatosis, multiple', 'multiple endocrine neoplasia type 1 syndrome', 'multiple endocrine neoplasia type I', 'multiple endocrine neoplasia, type 1', 'men type 1', 'multiple endocrine neoplasia caused by mutation in MEN1', 'multiple endocrine neoplasia, type I', 'endocrine adenomatosis multiple', 'multiple endocrine adenomatosis type I', 'multiple endocrine adenomatosis type 1', 'Wermer syndrome', 'men 1', 'MEA type I', 'multiple endocrine adenomatosis', 'MEN1 somatic mutations', 'MEN1 multiple endocrine neoplasia', 'MEA 1', 'men type I', 'multiple endocrine adenomatosis, type I', 'MEA type 1', 'multiple endocrine neoplasia type 1', 'multiple endocrine neoplasia 1', 'MEN1 syndrome', 'MEN1', 'Wermer^s syndrome']",10017,131100,652,C0025267,"['-0.0424', '0.2698', '-0.5293', '-0.637', '0.1713', '0.573', '0.336', '0.91', '-0.7554', '0.04068', '-0.3987', '0.3943', '-0.1245', '0.4836', '-0.6123', '-0.2913', '-0.2803', '-0.04327', '0.00961', '0.3804', '0.06155', '-0.6094', '0.1724', '-0.5283', '0.1705', '0.4353', '-0.0872', '-0.3796', '0.1677', '-0.283', '0.5527', '0.01035', '0.1415', '-0.638', '-0.3267', '-0.6123', '-0.625', '0.0928', '-0.5083', '0.4607', '0.428', '0.0447', '0.9937', '-0.6743', '0.7456', '-0.45', '-0.2944', '-0.275', '0.3818', '0.1465', '-0.03586', '0.3992', '0.0591', '-0.1968', '-0.5283', '0.668', '0.07306', '-0.134', '-0.3079', '0.718', '0.781', '0.9653', '0.0849', '-0.778', '-0.4165', '0.51', '0.10315', '0.7603', '-0.2563', '0.1251', '0.0634', '-0.3235', '0.4746', '-0.3997', '0.7637', '0.3516', '-0.3052', '0.349', '-0.0812', '-0.1373', '0.1132', '0.04892', '0.1738', '-0.0207', '-0.7227', '0.07886', '0.2112', '0.0427', '0.6577', '-0.4053', '-0.322', '0.0005946', '0.02779', '-0.514', '1.009', '0.3127', '0.4475', '-0.0251', '-0.382', '0.4573']",C3225,,D018761,258.01,,10028190,
mondo:0007541,"endometriosis, susceptibility to, 1","['endometriosis, susceptibility to, 1', 'ENDO1', 'endometriosis, susceptibility to, type 1']",,131200,,,,,,,,,,
mondo:0007542,Camurati-Engelmann disease,"['diaphyseal dysplasia 1, progressive', 'DPD1', 'diaphyseal dysplasia', 'Camurati-Englemann disease', 'CAEND', 'Engelman^s disease', 'CED', 'Camurati-Engelmann disease', 'Engelmann disease', 'progressive diaphyseal dysplasia', 'Camurati-Engelmann syndrome']",4997,131300,1328,C0011989,"['-0.6245', '0.217', '0.187', '-0.4617', '0.3252', '-0.3176', '0.2954', '0.897', '-0.918', '-0.166', '-0.4658', '0.08344', '0.2181', '0.1422', '0.263', '0.3953', '0.502', '0.012985', '-0.3188', '-0.636', '0.5347', '-0.3982', '0.2441', '-0.3088', '-0.421', '0.1494', '0.0355', '0.3555', '0.1555', '-0.2057', '0.3003', '-0.466', '-0.0442', '-0.08563', '-0.2778', '-0.455', '-0.995', '-0.4705', '-0.003569', '0.2556', '0.175', '-0.172', '-0.05194', '-0.2837', '0.6323', '0.2534', '0.2261', '0.3005', '0.4375', '-0.0932', '0.374', '0.4382', '0.2118', '-0.005733', '0.3003', '-0.4324', '0.334', '-0.3235', '-0.2451', '-0.2512', '0.2095', '0.27', '-0.529', '-0.717', '-0.0577', '-0.3386', '-0.0718', '0.4463', '0.0498', '0.2534', '-0.1536', '-0.3354', '-0.2104', '-0.5454', '0.6304', '0.5483', '0.03958', '0.04248', '0.3193', '-0.5205', '0.04416', '0.2212', '0.5938', '0.5327', '-0.3235', '0.2115', '0.1289', '0.04492', '0.161', '-0.05664', '-0.532', '0.1351', '0.174', '0.1165', '0.9272', '0.4937', '0.5947', '0.193', '0.2207', '0.0868']",C84610,,,756.59,,,
mondo:0007544,"eosinophilia, familial","['Eos', 'familial eosinophilia', 'eosinophilia, familial']",,131400,,,,,,C562722,,,,
mondo:0007545,Eosinophilopenia,"['Eosinophilopenia', 'eosinophil aplasia']",,131430,,C1851586,,,,,,,,
mondo:0007546,"myeloproliferative disorder, chronic, with eosinophilia","['eosinophils, malignant proliferation of', 'myeloproliferative disorder with eosinophilia', 'MPE', 'myeloproliferative disorder, chronic, with eosinophilia']",0111344,131440,,C1851585,,,,C565054,,,,
mondo:0007547,epidermoid cysts,"['infundibular cyst', 'epidermoid cyst', 'Epidermal cyst', 'squamous cyst', 'keratin cyst', 'keratinizing cyst', 'epidermal inclusion cyst', 'epithelial cyst', 'horn cyst', 'inclusion cyst', 'epidermoid cysts', 'keratinous cyst', 'Follicular infundibular cyst']",,131600,,,,C3134,1000243,D004814,,,,
mondo:0007548,transient bullous dermolysis of the newborn,"['DEB, bullous dermolysis of the newborn', 'dystrophic epidermolysis bullosa, neonatal', 'epidermolysis bullosa dystrophica, neonatal form', 'TBDN', 'transient bullous dermolysis of the newborn', 'transient bullous of the newborn', 'epidermolysis bullosa dystrophica, dominant neonatal form', 'DEB-BDN', 'MONDON']",0111345,131705,79411,C1851573,"['0.2242', '0.3557', '-0.8975', '0.0568', '0.2245', '-1.202', '-0.343', '0.505', '-0.04886', '-0.156', '-0.2245', '0.004482', '-0.4373', '-0.2637', '-0.03583', '-0.12085', '0.567', '-0.1495', '-0.0279', '-1.336', '-0.03348', '-0.2693', '0.308', '0.4688', '0.428', '0.1584', '-0.7593', '0.2229', '-0.7124', '0.2856', '0.635', '-0.2751', '-0.4038', '0.2886', '-0.2815', '-0.1537', '-0.7817', '-0.3103', '0.1338', '0.07404', '0.06183', '-0.5596', '0.1844', '0.1942', '-0.135', '-0.5015', '-0.1285', '-0.418', '0.2308', '0.01052', '0.028', '-0.639', '0.5645', '-0.0153', '-0.3113', '0.1139', '0.65', '0.6855', '0.004242', '0.196', '0.2361', '-0.04916', '-0.1932', '-0.2517', '0.2874', '0.008026', '1.03', '0.4805', '-0.859', '-0.0889', '-0.2612', '-0.3872', '0.1852', '0.3062', '0.4424', '0.11774', '-0.0969', '0.494', '-0.163', '-0.4172', '-0.1185', '-0.05695', '0.03677', '-0.742', '0.2698', '0.34', '-0.3967', '0.8647', '-0.2408', '0.11273', '0.3848', '0.876', '0.6074', '0.565', '0.1489', '1.234', '0.5073', '-0.547', '0.1459', '-0.408']",,,C536979,,,,
mondo:0007549,generalized dominant dystrophic epidermolysis bullosa,"['DDEB, Pasini and Cockayne-Touraine types', 'DDEB-gen', 'DDEB, generalised', 'epidermolysis bullosa dystrophica, AD', 'Albopapuloid dominant dystrophic epidermolysis bullosa', 'dominant dystrophic epidermolysis bullosa, generalised', 'autosomal dominant dystrophic epidermolysis bullosa, Pasini and Cockayne-Touraine types', 'dominant dystrophic epidermolysis bullosa, generalized', 'epidermolysis bullosa dystrophica, Pasini type', 'epidermolysis bullosa dystrophica, Pasini type (formerly)', 'dystrophic epidermolysis bullosa, autosomal dominant', 'autosomal dominant dystrophic epidermolysis bullosa', 'dominant dystrophic epidermolysis bullosa', 'epidermolysis bullosa dystrophica, autosomal dominant', 'epidermolysis bullosa dystrophica, Cockayne-Touraine type (formerly)', 'DDEB', 'DDEB, generalized', 'epidermolysis bullosa dystrophica, Cockayne-Touraine type', 'epidermolysis bullosa dystrophica with subcorneal cleavage']",0080224,131750,231568,,"['0.708', '0.10706', '-0.275', '-0.1793', '0.0891', '-0.3918', '-0.674', '0.201', '-0.1635', '-0.7627', '0.10126', '-0.4373', '-0.819', '0.526', '-0.7', '0.2637', '0.0993', '-0.781', '-0.1731', '-0.992', '-0.2505', '-0.214', '0.478', '0.564', '0.2554', '0.348', '-1.007', '0.6157', '-0.1147', '-0.828', '0.2888', '-0.1421', '-0.372', '-0.05914', '0.3325', '0.1796', '-0.964', '0.1407', '0.961', '-0.6714', '0.2103', '-0.4238', '0.238', '0.06116', '0.2305', '-0.4963', '-0.5425', '0.2263', '0.4192', '-0.308', '-0.4788', '-0.8086', '0.653', '-0.1415', '-0.4414', '-0.7207', '-0.21', '1.055', '-0.894', '-0.2546', '-0.1416', '0.508', '0.02043', '0.2942', '1.009', '0.5923', '0.225', '0.1893', '-0.5176', '0.326', '-0.3887', '0.0612', '-0.2888', '-0.05823', '0.0724', '-0.227', '-0.07324', '0.02988', '0.06726', '-0.2366', '-0.954', '0.12164', '-0.2705', '-0.2023', '0.05334', '0.5513', '-0.6826', '0.6074', '0.746', '0.3247', '-0.3418', '0.2197', '-0.1997', '0.5337', '-0.0772', '0.5786', '0.2974', '-0.6113', '0.805', '0.2074']",,,,757.39,,,
mondo:0007550,"epidermolysis bullosa simplex 1A, generalized severe","['epidermolysis bullosa herpetiformis, Dowling-Meara type', 'EBSDM', 'epidermolysis bullosa simplex, Dowling-Meara type', 'epidermolysis bullosa simplex, generalized severe', 'generalized severe epidermolysis bullosa simplex', 'epidermolysis bullosa simplex 1A, generalized severe', 'EBS-DM', 'EBS, generalised severe', 'epidermolysis bullosa simplex, generalised severe', 'epidermolysis bullosa simplex, herpetiformis', 'generalised severe epidermolysis bullosa simplex', 'epidermolysis bullosa simplex Dowling-Meara type', 'Dowling-Meara type epidermolysis bullosa simplex', 'EBS, generalized severe', 'EBS-gen sev', 'epidermolysis bullosa herpetiformis Dowling-Meara type']",0060735,131760,79396,,"['0.6963', '0.02101', '-0.4648', '0.10297', '0.005554', '-0.687', '-0.6274', '0.3857', '-0.06213', '-0.85', '0.10504', '-0.2262', '-0.786', '0.324', '-0.737', '0.003813', '0.173', '-0.9346', '-0.356', '-0.938', '-0.254', '-0.111', '0.3826', '0.568', '0.1704', '0.37', '-1.059', '0.8413', '-0.358', '-0.8267', '0.3445', '-0.3604', '-0.2386', '0.04623', '0.0562', '0.1205', '-1.049', '0.1307', '1.073', '-0.5005', '0.5186', '-0.4521', '0.3113', '-0.05054', '0.1086', '-0.0647', '-0.2986', '0.2832', '0.5664', '-0.1434', '-0.32', '-0.6123', '0.612', '-0.1133', '0.087', '-0.4792', '-0.03455', '1.248', '-0.8135', '-0.1959', '0.00668', '0.3677', '-0.0326', '0.2401', '1.009', '0.646', '0.3215', '0.3228', '-0.6904', '0.228', '-0.178', '0.1288', '-0.3984', '-0.0677', '-0.06354', '0.02449', '-0.1622', '0.1705', '0.02461', '-0.2527', '-0.788', '0.02925', '-0.2366', '-0.3025', '0.2644', '0.10223', '-0.745', '0.682', '0.9976', '0.1823', '-0.4622', '0.1813', '-0.01085', '0.597', '-0.05316', '0.702', '0.06885', '-0.6123', '0.8926', '0.06018']",,,,771.2,,,
mondo:0007551,"epidermolysis bullosa simplex 1C, localized","['localised epidermolysis bullosa simplex', 'epidermolysis bullosa simplex of palms and soles', 'Weber-Cockayne syndrome', 'epidermolysis bullosa simplex, Weber-Cockayne type', 'localized epidermolysis bullosa simplex', 'epidermolysis bullosa of hands and feet', 'EBS-loc', 'epidermolysis bullosa simplex, localised', 'epidermolysis bullosa simplex, localized', 'EBS, acral form', 'Weber-Cockayne type epidermolysis bullosa simplex', 'epidermolysis bullosa simplex 1C, localized']",0080510,131800,79400,,"['0.7554', '-0.002829', '-0.5864', '0.0616', '-0.07355', '-0.4485', '-0.5005', '0.618', '-0.1075', '-0.6177', '0.2064', '-0.2454', '-0.8306', '0.337', '-0.6714', '-0.06665', '0.05008', '-1.207', '-0.4878', '-0.907', '-0.3887', '-0.2104', '0.56', '0.5874', '0.2072', '0.485', '-1.067', '0.626', '-0.297', '-0.8213', '0.2527', '-0.3318', '-0.4487', '-0.003056', '-0.06323', '0.09705', '-1.195', '0.1625', '1.209', '-0.523', '0.4546', '-0.5464', '0.09656', '0.05872', '0.1926', '-0.12305', '-0.312', '0.2079', '0.4778', '0.0787', '-0.5103', '-0.606', '0.7217', '-0.01582', '-0.00588', '-0.3657', '0.004818', '1.147', '-0.5586', '-0.4585', '-0.1105', '0.326', '0.1699', '0.411', '0.902', '0.928', '0.4026', '0.2054', '-0.679', '0.3486', '-0.395', '-0.1302', '-0.4626', '0.0668', '0.05942', '0.1438', '-0.1597', '0.2502', '-0.04684', '-0.206', '-0.8794', '0.1837', '-0.2844', '-0.2228', '0.5366', '0.1654', '-0.869', '0.588', '1.146', '0.2695', '-0.5376', '0.2595', '-0.0661', '0.5913', '0.0629', '0.6494', '0.1858', '-0.777', '0.8823', '-0.1552']",,,,757.39,,,
mondo:0007552,pretibial dystrophic epidermolysis bullosa,"['pretibial epidermolysis bullosa', 'DEB-Pt', 'Deb, pretibial', 'dystrophic epidermolysis bullosa, pretibial', 'epidermolysis bullosa dystrophica, pretibial', 'epidermolysis bullosa, pretibial', 'pretibial DEB']",0080988,131850,79410,,"['0.616', '-0.0363', '-0.4485', '-0.08795', '0.0931', '-0.598', '-0.4634', '0.564', '-0.2286', '-0.534', '0.1077', '-0.448', '-0.854', '0.2445', '-0.5527', '0.3254', '0.1354', '-0.871', '-0.2502', '-0.838', '-0.4182', '-0.3044', '0.584', '0.636', '0.326', '0.4026', '-1.361', '0.7676', '-0.4011', '-0.7646', '0.11993', '-0.4683', '-0.3396', '0.05447', '0.07446', '-0.1477', '-0.917', '0.2144', '1.119', '-0.565', '0.287', '-0.6313', '0.18', '0.12317', '-0.002617', '-0.213', '-0.2428', '0.2383', '0.3513', '-0.4875', '-0.4243', '-0.7783', '0.554', '-0.1573', '0.03326', '-0.504', '-0.03442', '1.028', '-0.69', '-0.02301', '-0.04486', '0.354', '-0.0465', '0.5493', '0.944', '0.7686', '0.351', '0.502', '-0.5405', '0.3162', '-0.2036', '-0.09784', '-0.5156', '0.02284', '-0.1667', '0.1467', '-0.2062', '0.1572', '-0.06604', '-0.0465', '-0.9844', '0.1095', '-0.1114', '-0.0856', '0.2477', '0.1713', '-0.9526', '0.5635', '0.901', '0.2395', '-0.3738', '0.1827', '-0.08746', '0.759', '0.00216', '0.7144', '0.2147', '-0.4678', '0.764', '0.01787']",,,C535494,757.39,,,
mondo:0007553,epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase,['epidermolysis bullosa with deficiency of galactosylhydroxylysyl glucosyltransferase'],,131880,,C1851570,,,,C565049,,,,
mondo:0007554,"epidermolysis bullosa simplex 1B, generalized intermediate","['EBS, generalised', 'generalized epidermolysis bullosa simplex, non-Dowling-Meara type', 'generalized EBS, non-Dowling-Meara type', 'epidermolysis bullosa simplex, Kobner type', 'epidermolysis bullosa simplex, generalized', 'generalised EBS, non-Dowling-Meara type', 'EBS, generalised intermediate', 'EBS-K', 'generalised epidermolysis bullosa simplex, non-Dowling-Meara type', 'EBS, generalized intermediate', 'generalized EBS', 'EBS, generalized', 'epidermolysis bullosa simplex, generalized non-Dowling-Meara', 'generalised EBS', 'epidermolysis bullosa simplex, Koebner type', 'epidermolysis bullosa simplex, generalised non-Dowling-Meara', 'epidermolysis bullosa simplex, generalised intermediate', 'epidermolysis bullosa simplex, Köbner type', 'epidermolysis bullosa simplex 1B, generalized intermediate', 'epidermolysis bullosa simplex, generalised', 'epidermolysis bullosa simplex, generalized intermediate']",0080511,131900,79399,,"['0.806', '0.0731', '-0.3572', '0.0563', '0.0643', '-0.4302', '-0.398', '0.4448', '-0.07434', '-0.7485', '0.1888', '-0.6104', '-0.9336', '0.2664', '-0.5645', '0.1227', '0.0881', '-1.339', '-0.3848', '-0.8535', '-0.5444', '-0.1066', '0.5693', '0.7075', '0.1656', '0.4783', '-1.131', '0.596', '-0.3594', '-0.5806', '0.3093', '-0.2225', '-0.3298', '0.1284', '0.1869', '0.00949', '-1.067', '0.00623', '0.8906', '-0.624', '0.2668', '-0.8066', '0.0384', '-0.1472', '0.3044', '-0.2335', '-0.1494', '0.1584', '0.579', '-0.118', '-0.3767', '-0.7227', '0.665', '-0.1548', '0.133', '-0.522', '-0.2494', '1.158', '-0.6357', '-0.2627', '-0.1008', '0.285', '0.1746', '0.4575', '0.8726', '0.838', '0.2737', '0.2903', '-0.8306', '0.2942', '-0.1917', '-0.00593', '-0.4214', '-0.165', '0.1343', '0.3105', '-0.0412', '0.098', '-0.1086', '-0.3262', '-0.9287', '0.0983', '-0.3123', '-0.1776', '0.3572', '0.17', '-0.9746', '0.701', '1.035', '0.1597', '-0.41', '0.1744', '-0.1217', '0.5737', '-0.1332', '0.828', '0.1593', '-0.616', '0.721', '-0.0371']",,,,757.39,,,
mondo:0007555,"pidermolysis bullosa simplex 5A, Ogna type","['epidermolysis bullosa simplex, Ogna type', 'epidermolysis bullosa simplex 5A, Ogna type', 'EBSOG', 'EBS-Og', 'EBS-O']",0060736,131950,79401,,"['0.729', '-0.006145', '-0.3572', '-0.004776', '0.01567', '-0.721', '-0.562', '0.4167', '-0.01971', '-0.6772', '0.2634', '-0.444', '-0.7686', '0.3232', '-0.706', '0.0997', '0.1617', '-1.113', '-0.512', '-0.8726', '-0.2474', '0.05237', '0.3804', '0.5195', '0.3071', '0.334', '-1.112', '0.761', '-0.11273', '-0.8296', '0.1636', '-0.2622', '-0.2854', '-0.0279', '-0.007782', '0.07745', '-0.977', '0.1747', '1.145', '-0.671', '0.3958', '-0.579', '0.294', '-0.1844', '0.03934', '-0.11456', '-0.1323', '0.1882', '0.496', '-0.266', '-0.5576', '-0.7593', '0.541', '-0.1265', '0.2045', '-0.5923', '-0.2046', '1.137', '-0.879', '-0.1403', '-0.2488', '0.451', '0.05795', '0.328', '0.8774', '0.673', '0.2189', '0.05798', '-0.8', '0.2205', '-0.3154', '0.10504', '-0.637', '-0.06464', '-0.09174', '0.04105', '-0.2264', '0.3962', '0.05853', '-0.3196', '-0.8774', '-0.0548', '-0.2228', '-0.1342', '0.1566', '0.3855', '-0.943', '0.671', '1.039', '0.3306', '-0.3716', '0.1721', '0.04547', '0.694', '0.0462', '0.9863', '0.1394', '-0.55', '0.769', '0.03418']",,,C535962,757.39,,,
mondo:0007556,"epidermolysis bullosa simplex 2F, with mottled pigmentation","['epidermolysis bullosa simplex 2F, with mottled pigmentation', 'epidermolysis bullosa simplex with mottled pigmentation', 'EBSMP', 'EBS with mottled pigmentation', 'speckled hyperpigmentation, palmo-plantar punctate keratoses and childhood blistering', 'EBS-MP', 'speckled hyperpigmentation with punctate palmoplantar keratoses and childhood blistering']",0111346,131960,79397,,"['0.614', '-0.0612', '-0.398', '-0.06573', '-0.045', '-0.5947', '-0.5513', '0.4673', '-0.2003', '-0.8345', '0.3381', '-0.389', '-0.9463', '0.3435', '-0.689', '0.1194', '0.2056', '-1.047', '-0.4412', '-0.9307', '-0.2742', '-0.1547', '0.4006', '0.4429', '0.164', '0.2566', '-1.059', '0.6973', '-0.312', '-0.6855', '0.2389', '-0.428', '-0.1617', '-0.11475', '-0.12286', '0.1004', '-1.118', '0.01172', '1.166', '-0.468', '0.5312', '-0.7764', '0.0732', '0.05478', '0.02481', '-0.2595', '-0.1881', '0.1709', '0.65', '-0.1119', '-0.3652', '-0.6885', '0.621', '-0.1119', '0.1263', '-0.5767', '-0.05997', '1.048', '-0.7007', '-0.2932', '-0.1077', '0.3132', '0.1605', '0.1298', '0.6465', '0.8813', '0.4436', '0.2874', '-0.768', '0.3325', '-0.3328', '0.001232', '-0.4348', '-0.0539', '-0.05383', '0.1167', '-0.18', '0.1775', '0.002338', '-0.1819', '-0.7437', '0.04404', '-0.3486', '-0.0932', '0.3052', '0.2477', '-0.9033', '0.5874', '1.09', '0.2305', '-0.4448', '0.2827', '0.1807', '0.59', '0.08606', '0.75', '0.2267', '-0.499', '0.6777', '0.001491']",,,C535959,757.39,,,
mondo:0007557,epidermolysis bullosa with congenital localized absence of skin and deformity of nails,"['epidermolysis bullosa with congenital localized absence of skin and deformity of nails', 'EBD, Bart type', 'epidermolysis bullosa dystrophica, Bart type']",0111347,132000,,,,,,C562638,757.39,,,
mondo:0007558,benign occipital epilepsy,"['epilepsy, benign occipital', 'BOE']",,132090,25968,C1851549,,,,,,,,
mondo:0007559,photoparoxysmal response 1,"['photoparoxysmal response 1', 'photosensitivity', 'PPR1', 'epilepsy, photogenic', 'Ppr', 'Photoconvulsive reaction']",,132100,,C1868677,,,,,,,,
mondo:0007560,reading seizures,"['epilepsy, reading']",,132300,166433,C0278193,,,,,,,,
mondo:0007561,multiple epiphyseal dysplasia type 1,"['Polyepiphyseal dysplasia type 1', 'epiphyseal dysplasia, Fairbank type', 'multiple epiphyseal dysplasia, Comp-related', 'epiphyseal dysplasia, multiple, type 1', 'COMP multiple epiphyseal dysplasia (disease)', 'epiphyseal dysplasia multiple 1', 'multiple epiphyseal dysplasia COMP-related', 'MED1', 'multiple epiphyseal dysplasia 1', 'epiphyseal dysplasia, ribbing type', 'EDM1', 'epiphyseal dysplasia, multiple, 1']",0070303,132400,93308,C4275061,"['-0.3933', '0.3848', '0.0956', '-0.5767', '0.4758', '-0.6455', '-0.0987', '0.725', '-0.8716', '-0.2874', '-0.02086', '0.3171', '-0.1327', '0.239', '0.2229', '0.0798', '0.1877', '-0.00853', '-0.1462', '-0.4534', '-0.0538', '-0.0374', '0.523', '0.06586', '0.2433', '0.6226', '0.148', '-0.2874', '-0.204', '-0.09546', '0.1345', '-0.1434', '0.03223', '0.3687', '0.08527', '-0.1211', '-0.3596', '-0.1742', '0.077', '-0.03976', '0.3735', '-0.3367', '-0.0714', '0.25', '0.2247', '-0.4656', '-0.2642', '0.01246', '0.1641', '-0.4243', '0.3105', '0.154', '-0.01435', '-0.1771', '-0.1188', '-0.8667', '0.005283', '-0.491', '-0.1316', '-0.3804', '0.46', '0.0957', '-0.3704', '-0.066', '0.07715', '0.2786', '0.2257', '0.14', '0.2095', '-0.11255', '-0.2766', '-0.0902', '0.2527', '-0.5835', '0.4387', '0.4827', '-0.3486', '0.5527', '-0.2542', '-0.4175', '0.12036', '0.1378', '0.010445', '0.1821', '-0.09674', '0.667', '0.0775', '0.2465', '0.2883', '0.3042', '-0.3025', '0.2517', '0.0844', '-0.01819', '0.4714', '0.0648', '0.726', '-0.3027', '0.03726', '0.0898']",,,,,Q77.3,,
mondo:0007562,"multiple epiphyseal dysplasia, Beighton type","['multiple epiphyseal dysplasia-myopia-deafness syndrome', 'epiphyseal dysplasia, multiple, with myopia and conductive deafness', 'epiphyseal dysplasia, multiple, with myopia and deafness', 'EDMMD']",0111348,132450,166011,,,,,C565046,,Q77.3,,
mondo:0007564,pilomatrixoma,"['benign pilomatrixoma', 'benign pilomatricoma', 'epithelioma calcificans of Malherbe', 'calcifying Epitherlioma of Malherbe', 'pilomatrixoma, benign', 'pilomatricoma', 'pilomatricoma, somatic', 'calcifying epithelioma of Malherbe', 'pilomatrixoma', 'PTR', 'benign hair follicle neoplasm']",5374,132600,91414,C0853031,"['-0.01868', '0.02187', '-0.00886', '-0.00829', '0.01218', '-0.0333', '0.00555', '0.03204', '-0.03436', '-0.00816', '-0.00533', '-0.01646', '0.00563', '0.01162', '-0.01982', '-0.01982', '-0.004196', '-0.02153', '-0.000969', '-0.0594', '-0.00789', '-0.027', '0.02177', '-0.004997', '0.006294', '-0.02345', '-0.01654', '-0.01522', '0.00842', '-0.014244', '0.04587', '0.00348', '0.02156', '0.002726', '0.01214', '-0.0099', '-0.02348', '-0.00594', '-0.00551', '-0.046', '0.012184', '-0.0523', '0.00939', '-0.02336', '0.000598', '-0.04227', '-0.0041', '0.02827', '0.011314', '0.013214', '-0.01029', '-0.00161', '0.008736', '0.00879', '-0.0341', '-0.02696', '0.03348', '-0.01909', '-0.05362', '0.005688', '0.01266', '0.013306', '0.007114', '0.002853', '0.004555', '-0.003998', '0.04825', '0.0209', '-0.04318', '0.0423', '-0.02411', '0.004974', '0.02356', '-0.00885', '0.001458', '0.0339', '-0.00968', '0.004578', '-0.02135', '-0.01643', '-0.002779', '-0.010376', '-0.00482', '0.0262', '-0.00933', '-0.005405', '-0.00327', '0.03253', '0.04453', '0.01733', '0.013275', '0.02538', '0.00295', '0.01923', '0.0747', '0.02058', '0.02794', '-0.03058', '-0.01195', '0.007656']",C7368,0009082,D018296,,,10035040,
mondo:0007565,familial cylindromatosis,"['^turban tumor^ syndrome', 'Ancell-Spiegler Cylindromas', 'CYLD', 'cylindromatosis, familial', 'Cylindromas, dermal eccrine', 'turban tumors', 'turban tumours', 'turban tumor', 'turban tumour', 'turban tumor syndrome', 'Ancell-Spiegler syndrome', 'turban tumour syndrome']",,132700,211,,"['-0.02711', '0.06238', '0.001468', '-0.01855', '0.01794', '-0.0756', '0.000901', '0.067', '-0.05173', '-0.00999', '0.0004182', '-0.03143', '-0.02147', '0.02101', '-0.04974', '-0.049', '-0.02899', '-0.03204', '0.0235', '-0.1152', '-0.000499', '-0.02335', '0.03888', '-0.03592', '0.03128', '-0.01207', '-0.0003498', '-0.011116', '-0.003414', '-0.0326', '0.09235', '-0.01354', '0.0741', '0.0336', '0.02336', '-0.0348', '-0.01616', '-0.02919', '-0.00681', '-0.0929', '0.05472', '-0.06226', '0.03064', '-0.02849', '-0.001515', '-0.05386', '-0.02216', '0.0672', '0.01282', '0.03186', '-0.0209', '0.00959', '0.00666', '0.03284', '-0.03842', '-0.01243', '0.0821', '-0.08246', '-0.10114', '-0.005367', '0.0515', '0.04535', '0.002502', '-0.002981', '0.00504', '0.00802', '0.0902', '0.03983', '-0.06143', '0.07184', '-0.0411', '0.02017', '0.02751', '-0.0467', '0.0373', '0.05597', '0.01988', '0.03122', '-0.04413', '-0.0484', '0.005257', '0.03305', '-0.0158', '0.03128', '0.00814', '-0.0135', '0.02945', '0.0436', '0.07855', '-0.007553', '0.0278', '0.03094', '-0.01037', '0.002054', '0.1407', '0.02748', '0.0744', '-0.11743', '-0.07935', '0.007694']",C43352,,C536611,,,,
mondo:0007566,multiple self-healing squamous epithelioma,"['Ferguson-Smith-type epithelioma', 'MSSE', 'Ferguson-Smith disease', 'multiple self healing squamous epithelioma', 'Ferguson-Smith type epithelioma', 'Ferguson-Smith tumour', 'Ferguson-Smith tumor', 'multiple self healing epithelioma of Ferguson-Smith', 'multiple self-healing squamous epithelioma, susceptibility to', 'familial primary self-healing squamous epithelioma of the skin, Ferguson-Smith type', 'ESS1, formerly', 'self-healing squamous epithelioma type 1', 'multiple keratoacanthoma, Ferguson-Smith type', 'ESS1', 'ESS1 (formerly)', 'multiple self-healing epithelioma of Ferguson-Smith']",5585,132800,65748,C0345982,"['0.4797', '0.1451', '-0.6113', '0.42', '0.1945', '-0.4668', '0.1346', '0.2593', '-0.1917', '-0.1136', '0.3936', '0.523', '-0.2145', '0.11835', '-0.08136', '0.152', '0.2651', '-0.2401', '0.3816', '-0.3293', '-0.327', '0.2827', '0.713', '-0.353', '0.2012', '0.09393', '-0.792', '0.1602', '-0.3', '0.02985', '0.7925', '-0.4297', '0.1406', '-0.4746', '0.2318', '-0.09894', '-0.055', '-0.3975', '-0.05945', '-0.2185', '0.2664', '-0.3367', '-0.01342', '-0.4443', '0.265', '-0.1593', '-0.6816', '0.2705', '0.10754', '-0.3137', '0.05823', '0.1626', '0.03607', '0.3176', '-0.608', '0.3198', '0.3694', '0.162', '-0.3416', '0.0865', '-0.2307', '0.12164', '-0.642', '0.1907', '-0.1117', '-0.0771', '0.3835', '0.6084', '-0.0676', '1.012', '0.5225', '-0.08374', '0.387', '0.25', '0.11536', '-0.03452', '-0.4382', '-0.218', '-0.3677', '-1.053', '-0.3374', '0.02864', '0.5503', '0.09204', '-0.3135', '-0.1976', '0.2656', '0.2644', '0.303', '-0.1462', '0.261', '0.3013', '0.07776', '0.3142', '0.3545', '0.3557', '0.2644', '-0.2222', '0.0827', '-0.03806']",C4461,,C536150,,,,
mondo:0007568,"aortic aneurysm, familial thoracic 4","['aortic aneurysm, familial thoracic type 4', 'FAA4', 'familial thoracic aortic aneurysm and aortic dissection caused by mutation in MYH11', 'MYH11 familial thoracic aortic aneurysm and aortic dissection', 'aortic aneurysm, familial thoracic 4', 'AAT4', 'aortic aneurysm/aortic dissection and patent ductus arteriosus']",,132900,,C1851504,,,,C537784,,,,
mondo:0007569,"erythema nodosum, familial","['erythema nodosum, familial', 'familial erythema nodosum']",,132990,,C1851503,,,,C535510,,,,
mondo:0007570,erythema palmare hereditarium,"['erythema palmare hereditarium', 'lane disease', 'Red palms disease']",,133000,231031,C1851502,,,,C565041,,,,
mondo:0007571,primary erythermalgia,"['erythromelalgia, primary', 'small fibre neuropathy', 'erythromelalgia, familial', 'neuropathy, small fiber', 'primary erythromelalgia', 'PERYTHM', 'small fiber neuropathy', 'erythermalgia, primary', 'neuropathy, small fibre', 'Mitchell disease (formerly)']",,133020,90026,C0014805,"['-0.0929', '-0.617', '-0.3953', '0.02385', '-0.2612', '-0.0436', '0.0969', '0.1754', '-0.1193', '-0.2878', '-0.1276', '0.1348', '-0.1009', '0.2391', '-0.5103', '0.2438', '-0.2083', '-0.4248', '0.3696', '-0.5273', '0.1431', '-0.779', '-0.0726', '-0.04208', '-0.455', '-0.147', '-0.2129', '0.09247', '-0.3745', '-0.342', '-0.372', '0.00418', '-0.0728', '-0.1382', '-0.0371', '-0.324', '0.2263', '-0.3806', '0.591', '-0.2024', '0.05908', '-0.5786', '0.3882', '-0.0919', '0.6', '0.0001478', '-0.464', '0.6357', '0.1819', '0.2998', '-0.2598', '-0.1362', '0.0688', '0.02394', '0.279', '-0.1422', '0.772', '-0.1098', '-0.6724', '-0.141', '0.3674', '0.3347', '-0.0367', '-0.0959', '-0.2227', '0.0735', '0.3857', '0.8555', '0.304', '-0.1414', '-0.586', '-0.648', '0.2175', '0.3352', '0.704', '0.987', '0.1181', '0.3247', '0.02214', '-0.3884', '-0.243', '-0.2067', '0.3293', '-0.04916', '0.1271', '0.1495', '-0.07965', '0.3147', '0.4414', '0.1791', '0.4033', '-0.3274', '0.05444', '0.1466', '0.2942', '-0.1404', '0.161', '-0.935', '-0.3975', '-0.3533']",C125383,,,,,,
mondo:0007572,primary familial polycythemia due to EPO receptor mutation,"['PFCP', 'autosomal dominant benign erythrocytosis', 'congenital polycythemia due to erythropoietin receptor mutation', 'erythrocytosis, familial, 1', 'primary familial and congenital polycythemia', 'familial erythrocytosis type 1', 'primary congenital erythrocytosis', 'polycythemia, primary familial and congenital', 'erythrocytosis, autosomal dominant benign', 'familial erythrocytosis, 1', 'erythrocytosis, familial, type 1', 'familial erythrocytosis', 'EPOR familial polycythemia', 'familial erythrocytosis 1', 'primary familial polycythemia', 'erythrocytosis, somatic', 'ECYT1', 'erythrocytosis autosomal dominant benign', 'familial polycythemia caused by mutation in EPOR', 'congenital erythrocytosis due to erythropoietin receptor mutation']",0060652,133100,90042,,"['-0.1581', '-0.076', '-0.571', '-0.1831', '0.08435', '0.4739', '-0.1954', '0.499', '0.335', '0.01348', '-0.05716', '0.1849', '0.2208', '0.03943', '-0.1399', '0.2356', '-0.1998', '-0.1262', '0.1582', '-0.4385', '0.2883', '-0.4604', '0.3884', '0.10944', '0.6235', '0.151', '0.05902', '0.02275', '-0.4639', '0.2147', '0.8325', '-0.11786', '0.653', '0.4534', '-0.4812', '-0.08374', '-0.275', '-0.2241', '0.4111', '-0.8716', '0.05383', '0.3225', '0.8003', '-0.9897', '0.0586', '-0.1569', '0.1992', '0.2605', '0.253', '-0.3967', '0.4214', '0.315', '-0.00875', '0.2578', '-0.0315', '0.1606', '0.4053', '-0.3682', '-0.583', '0.1101', '0.2009', '0.4353', '0.3992', '-0.8086', '-0.1891', '0.0497', '-0.1682', '0.7266', '-0.4053', '0.7256', '-0.02391', '-0.1065', '-0.5195', '-0.1658', '0.7944', '0.1266', '0.3252', '-0.1495', '0.1647', '-0.122', '-0.04712', '-0.08295', '0.2081', '-0.06082', '0.12494', '-0.2207', '0.311', '0.1393', '0.522', '-0.0874', '0.2092', '-0.06052', '-0.5747', '0.3035', '0.626', '0.1501', '0.2563', '-0.2874', '-0.4417', '0.09064']",,,,289.6,,,
mondo:0007573,"erythroleukemia, familial, susceptibility to","['ERYTHROLEUKEMIA, familial', 'leukemia, acute myelogenous, M6', 'hereditary acute erythroid leukemia', 'hereditary acute erythroid leukaemia', 'erythroleukemia, familial, susceptibility to', 'Di Guglielmo disease, familial']",,133180,,,"['-0.02072', '0.03586', '-0.0176', '0.00074', '0.01095', '-0.0525', '-0.001121', '0.06335', '-0.0875', '-0.001303', '-0.00994', '-0.0241', '-0.012245', '0.04468', '-0.04907', '-0.04388', '-0.007015', '-0.03894', '0.02435', '-0.1326', '0.001718', '-0.0364', '0.0636', '-0.0517', '-0.002367', '-0.02127', '-0.0005016', '-0.0161', '-0.00698', '-0.05057', '0.03766', '0.00887', '0.07184', '0.01776', '0.01189', '0.0091', '-0.0174', '-0.02966', '-0.00868', '-0.061', '0.02165', '-0.04535', '0.02904', '-0.01255', '-0.01193', '-0.03275', '-0.02698', '0.04105', '0.013626', '0.02675', '-0.007812', '-0.004333', '0.03026', '0.00505', '-0.01435', '-0.03123', '0.0668', '-0.04254', '-0.07587', '0.00887', '0.04205', '0.0393', '0.02388', '-0.03473', '0.01093', '0.02658', '0.0727', '0.06305', '-0.0449', '0.0705', '-0.03714', '0.01114', '-0.0006127', '-0.05847', '0.0318', '0.04587', '0.0307', '0.015144', '-0.03342', '-0.03357', '-0.00873', '-0.01413', '-0.03906', '0.02328', '0.001558', '-0.013054', '0.024', '0.04535', '0.0683', '-0.002325', '0.04193', '0.0349', '-0.01319', '-0.006096', '0.10455', '0.0568', '0.08093', '-0.08984', '-0.03775', '0.01188']",,0000218,C565039,207.0,,,
mondo:0007574,spinocerebellar ataxia type 34,"['SCA34', 'erythrokeratodermia with ataxia', 'erythrokeratodermia - ataxia', 'spinocerebellar ataxia 34', 'spinocerebellar ataxia type 34', 'Giroux Barbeau syndrome', 'spinocerebellar ataxia and erythrokeratodermia']",0050981,133190,1955,C1851481,"['-0.1469', '-0.09283', '-0.5083', '0.0655', '-0.10913', '-0.795', '-0.0429', '0.08', '-0.6133', '-0.9453', '0.05566', '0.2268', '0.12494', '0.2698', '0.597', '-0.2023', '-0.1887', '-0.2922', '0.2737', '-0.822', '0.001728', '-0.3574', '0.01897', '-0.305', '0.2133', '-0.5254', '-0.3547', '0.1708', '-0.03186', '-0.7715', '0.2357', '0.3704', '-0.267', '-0.06464', '0.4238', '0.08136', '0.03342', '0.0636', '0.516', '0.4346', '0.2462', '0.2079', '-0.3386', '0.549', '0.5947', '-0.6157', '0.02155', '0.217', '0.251', '-0.259', '-0.1337', '-0.0317', '0.0626', '-0.5396', '-0.2295', '-0.597', '0.5347', '0.4927', '-0.2401', '0.3157', '-0.608', '0.1908', '0.2308', '-0.154', '-0.4949', '0.546', '0.2876', '0.504', '-0.5176', '0.3901', '0.714', '0.447', '-0.1691', '-0.8315', '0.678', '0.2651', '0.1797', '-0.1508', '0.03812', '0.558', '-0.2576', '-0.9233', '0.62', '0.514', '-0.266', '-0.6807', '0.2878', '-0.0598', '0.578', '0.3792', '0.4102', '0.553', '0.0857', '0.1935', '0.849', '0.8525', '0.2937', '0.3943', '-0.113', '0.03406']",,,C535738,,,,
mondo:0007576,esophageal cancer,"['esophageal carcinoma, somatic', 'malignant neoplasm of upper third oesophagus', 'esophageal cancer, somatic', 'malignant esophageal tumor', 'malignant neoplasm of upper third esophagus', 'malignant neoplasm of the oesophagus', 'esophageal squamous cell carcinoma, susceptibility to', 'malignant neoplasm of middle third of oesophagus', 'malignant tumour of the oesophagus', 'malignant neoplasm of proximal third of oesophagus', 'malignant esophagus neoplasm', 'malignant oesophagus tumour', 'Ca middle third esophagus', 'esophagus cancer', 'malignant oesophagus neoplasm', 'malignant esophageal neoplasm', 'Escc, susceptibility to', 'Ca middle third oesophagus', 'cancer of esophagus', 'cancer of oesophagus', 'oesophagus cancer', 'malignant neoplasm of the esophagus', 'malignant tumor of proximal third of esophagus', 'malignant tumour of abdominal oesophagus', 'gastric cardia adenocarcinoma, susceptibility to', 'malignant esophageal tumour', 'malignant neoplasm of distal third of oesophagus', 'malignant neoplasm of distal third of esophagus', 'malignant tumor of the middle third of the esophagus', 'malignant neoplasm of esophagus', 'malignant esophagus tumor', 'Aerodigestive tract cancer, susceptibility to', 'malignant tumour of proximal third of oesophagus', 'malignant neoplasm of oesophagus', 'malignant neoplasm of middle third of esophagus', 'malignant neoplasm of lower third of esophagus', 'malignant neoplasm of lower third of oesophagus', 'malignant tumor of the esophagus', 'malignant tumour of oesophagus', 'esophageal cancer', 'Ca lower third oesophagus', 'Ca lower third esophagus', 'malignant tumor of abdominal esophagus', 'malignant tumour of the middle third of the oesophagus', 'esophageal squamous cell carcinoma, somatic', 'malignant neoplasm of proximal third of esophagus', 'malignant tumor of distal third of esophagus', 'malignant tumor of esophagus', 'malignant tumour of distal third of oesophagus']",5041,133239,,C0546837,"['0.012085', '0.02461', '0.001329', '-0.01005', '-0.001166', '-0.03735', '0.01582', '0.03217', '-0.03001', '-0.01797', '-0.002344', '-0.00812', '-0.01483', '0.01216', '-0.02812', '-0.0352', '0.001218', '-0.02625', '-0.008446', '-0.08417', '-0.01425', '-0.015434', '0.01738', '-0.02333', '0.0362', '-0.01712', '-0.011986', '0.0001569', '-0.00991', '-0.0406', '0.03793', '-0.02478', '0.03076', '-0.01923', '0.02887', '0.006706', '-0.01447', '-0.02058', '-0.006268', '-0.02325', '0.01336', '-0.04663', '0.00986', '-0.02585', '-0.004436', '-0.01585', '-0.0229', '0.04514', '0.02075', '0.02231', '-0.02939', '0.00904', '0.00735', '0.00853', '-0.0264', '-0.01616', '0.04196', '-0.003113', '-0.0653', '-0.01982', '0.039', '0.02388', '-0.007114', '0.000438', '0.00689', '0.013535', '0.04794', '0.02475', '-0.03284', '0.04645', '-0.02524', '0.0088', '0.007603', '-0.01564', '0.02434', '0.003548', '0.012146', '-0.02872', '-0.0346', '-0.03058', '-0.01732', '0.0002515', '-0.0164', '0.013725', '-0.02037', '-0.02287', '0.01825', '0.03333', '0.0507', '0.000944', '-0.01297', '0.04437', '-0.00535', '-0.0069', '0.0703', '0.00793', '0.03613', '-0.03485', '-0.01224', '0.00201']",C7478,,,150.9,,,
mondo:0007577,"esophageal ring, lower","['esophageal ring, lower']",,133240,,C0341137,,,,C562765,750.3,,,
mondo:0007581,"exchondrosis of pinna, posterior","['exchondrosis of pinna, posterior', 'Ear bump']",,133500,,C1851463,,,,C565036,,,,
mondo:0007584,exostoses-anetodermia-brachydactyly type E syndrome,"['exostoses with anetodermia and brachydactyly, type E']",,133690,1962,C1851428,,,,C565034,,,,
mondo:0007585,"exostoses, multiple, type 1","['multiple cartilaginous exostoses', 'diaphyseal Aclasis', 'EXT1 exostoses, multiple', 'exostoses, multiple, type I', 'exostoses, multiple caused by mutation in EXT1', 'EXT', 'osteochondromatosis', 'multiple osteochondromas']",,133700,,,,,,,,,,
mondo:0007586,"exostoses, multiple, type 2","['Ext2', 'EXT2 Gene', 'exostoses (Multiple) 2 Gene', 'exostoses, multiple, type II', 'exostoses, multiple caused by mutation in EXT2', 'EXT2 exostoses, multiple']",,133701,,C1851413,,C18252,,,,,,
mondo:0007587,external auditory canal atresia-vertical talus-hypertelorism syndrome,"['external auditory canal, bilateral atresia of, with congenital vertical talus', 'Rasmussen Johnsen Thomsen syndrome', 'inherited congenital bilateral atresia of the external auditory canal, congenital bilateral vertical talus and increased interocular distance', 'Rasmussen-Johnsen-Thomsen syndrome', 'Rasmussen syndrome']",,133705,3023,C2930867,,,,,,,,
mondo:0007588,extrasystoles-short stature-hyperpigmentation-microcephaly syndrome,"['Char-Douglas-Dungan syndrome', 'extrasystoles, multiform ventricular, with short stature, hyperpigmentation and microcephaly']",,133750,1964,C1851412,,,,C565032,,,,
mondo:0007589,exudative vitreoretinopathy 1,"['exudative vitreoretinopathy 1', 'exudative vitreoretinopathy type 1', 'FEVR, autosomal dominant', 'EVR1', 'retinopathy of prematurity', 'Criswick-Schepens syndrome', 'exudative vitreoretinopathy, familial, autosomal dominant']",0111412,133780,90050,C1851402,,C175048,,C536382,,,,
mondo:0007590,hemifacial hypertrophy,"['hemifacial hypertrophy', 'facial asymmetry', 'hemifacial hyperplasia', 'facial hemihypertrophy']",,133900,141145,C1399354,,,,,,,,
mondo:0007592,familial recurrent peripheral facial palsy,"['familial recurrent Bell palsy', 'facial palsy, familial recurrent peripheral']",,134200,2809,C1851399,,,,C565028,,G51.0,,
mondo:0007593,facial spasm,['facial spasm'],,134300,,,,,,,,,,
mondo:0007594,factor 5 excess with spontaneous thrombosis,"['thrombophilia with elevated Factor 5', 'factor V excess with spontaneous thrombosis', 'Proaccelerin Excess']",,134400,,C1851378,,,,C565026,,,,
mondo:0007595,"factor VII and Factor VIII, combined deficiency of","['factor VII and Factor VIII, combined deficiency of', 'familial multiple coagulation Factor deficiency 4', 'multiple coagulation Factor deficiency 4', 'factor 7 and Factor VIII, combined deficiency of']",,134430,,C1851377,,,,C565025,,,,
mondo:0007597,"factor VIII and Factor IX, combined deficiency of","['familial multiple coagulation Factor deficiency 2', 'factor VIII and factor IX, combined deficiency OF', 'factor VIII and Factor IX, combined deficiency of', 'F8F9D', 'factor 8 and Factor IX, combined deficiency of']",,134510,,C1851376,,,,C565024,,,,
mondo:0007598,"factors VIII, IX and XI, combined deficiency of","['factors VIII, IX and XI, combined deficiency of', 'factors VIII, 9 and Xi, combined deficiency of', 'familial multiple coagulation Factor deficiency 5', 'multiple coagulation Factor deficiency 5']",,134520,,C1851375,,,,C565023,,,,
mondo:0007599,"factor 9 and Factor XI, combined deficiency of","['multiple coagulation Factor deficiency 6', 'factor IX and factor XI, combined deficiency OF', 'familial multiple coagulation Factor deficiency 6']",,134540,,C1851374,,,,C565022,,,,
mondo:0007600,primary Fanconi syndrome,"['FRTS1', 'Fanconi renotubular syndrome 1', 'primary Fanconi renotubular syndrome']",,,,,,C123229,,,,,,
mondo:0007601,"familial Mediterranean fever, autosomal dominant","['Fmf, autosomal dominant', 'familial Mediterranean fever, AD', 'familial Mediterranean fever, autosomal dominant']",,134610,,C1851347,,,,C565021,,,,
mondo:0007603,Felty syndrome,"['familial Felty^s syndrome', 'rheumatoid arthritis, splenomegaly and neutropenia', 'Felty^s syndrome', 'rheumatoid arthritis with splenoadenomegaly and leukopenia', 'splenomegaly-neutropenia-rheumatoid arthritis syndrome', 'Felty syndrome']",11042,134750,47612,C0015773,,C84712,0007269,D005258,714.1,,10016386,
mondo:0007604,femoral-facial syndrome,"['femoral facial syndrome', 'femoral dysgenesis, bilateral', 'FHUFS', 'femoral hypoplasia unusual facies syndrome', 'femoral hypoplasia-unusual facies syndrome', 'femoral-facial syndrome', 'FFS']",,134780,1988,,,,,C537916,759.89,,,
mondo:0007605,fibrinolytic defect,['fibrinolytic defect'],,134900,,C1851184,,,,C565017,,,,
mondo:0007606,fibrodysplasia ossificans progressiva,"['Stone man syndrome', 'progressive ossifying myositis', 'Stone Man syndrome', 'myositis ossificans progressiva', 'progressive myositis ossificans', 'fibrodysplasia ossificans progressiva', 'fop']",13374,135100,337,C0016037,"['-0.405', '-0.375', '-0.594', '0.00501', '0.09735', '-0.708', '0.1917', '0.3643', '-0.2805', '0.3813', '-0.1753', '-0.1863', '0.09894', '0.2493', '-0.0793', '0.7085', '0.248', '-0.4077', '-0.1815', '-0.2966', '0.34', '0.0633', '0.4602', '-0.08264', '0.4736', '-0.1873', '-0.1631', '-0.06793', '-0.3884', '-0.7554', '0.07623', '-0.07025', '-0.02641', '0.636', '0.1597', '0.2347', '0.7524', '-0.4766', '0.311', '-0.36', '0.004864', '-0.4954', '-0.14', '0.386', '0.8203', '0.0637', '-0.486', '0.604', '-0.1389', '0.317', '-0.1317', '-0.516', '0.604', '0.0367', '0.2367', '-0.3499', '0.7725', '0.1871', '-0.1915', '0.6235', '0.4216', '0.5405', '-0.8677', '0.515', '0.172', '0.006878', '0.1569', '0.1826', '-0.723', '0.2712', '-0.06323', '-0.2292', '0.1003', '-0.5425', '1.005', '-0.3374', '0.212', '0.07074', '-0.3188', '-0.3628', '-0.134', '-0.4285', '0.0673', '-0.069', '-0.2534', '-0.0688', '0.2083', '-0.03296', '-0.4841', '0.0404', '0.3262', '0.403', '-0.1643', '-0.07117', '0.2554', '0.1943', '0.976', '-0.3145', '0.0902', '-0.2241']",C3040,,D009221,728.11,,10068715,
mondo:0007607,Birt-Hogg-Dube syndrome,"['Birt-Hogg-Dube syndrome', 'Birt-Hogg-Dubé syndrome', 'Hornstein-Knickenberg syndrome', 'BHD syndrome', 'Birt Hogg Dube syndrome', 'BHD', 'fibrofolliculomas with trichodiscomas and acrochordons']",0050676,135150,122,C0346010,"['-0.1672', '0.2979', '-0.942', '0.0899', '0.1439', '-0.4453', '0.1118', '0.1515', '0.04965', '-0.1337', '-0.0007086', '-0.324', '-0.3389', '0.287', '-0.3872', '-0.2286', '0.1458', '-0.2559', '0.04904', '-0.371', '-0.3992', '-0.4211', '0.8525', '-0.6187', '0.0997', '0.003754', '-0.6187', '0.3892', '-0.01397', '0.1043', '1.303', '-0.559', '-0.2389', '-0.2461', '0.2245', '0.1696', '-0.1483', '0.09656', '-0.10876', '-0.1099', '-0.0434', '-0.1843', '0.616', '-0.6235', '0.4082', '-0.1555', '-0.576', '-0.4907', '0.2607', '-0.4075', '0.0903', '0.1475', '0.3088', '0.0683', '-0.10815', '-0.0774', '0.2778', '0.22', '-0.765', '0.10175', '0.398', '0.2277', '-0.272', '-0.1649', '0.006557', '-0.1343', '0.4768', '0.8506', '-0.4265', '1.265', '-0.1434', '-0.659', '0.1176', '0.313', '0.12146', '-0.6304', '-0.2131', '0.4429', '-0.1613', '-0.5557', '0.0881', '0.1421', '0.2461', '0.3125', '-0.5874', '0.1069', '0.4958', '0.671', '-0.2646', '0.04526', '0.2656', '0.09674', '-0.4844', '-0.02043', '0.875', '-0.6646', '0.5947', '-0.4119', '-0.3794', '0.2522']",C28244,1001273,D058249,704.8,,10067736,
mondo:0007608,desmoid tumor,"['desmoid-type fibromatosis', 'FIF', 'deep fibromatosis/desmoid tumor', 'aggressive fibromatosis', 'desmoid disorder, hereditary', 'desmoid disease, hereditary', 'familial infiltrative fibromatosis', 'deep fibromatosis/desmoid tumour', 'desmoid fibromatosis', 'desmoid/aggressive fibromatosis', 'fibromatosis, familial infiltrative', 'deep fibromatosis', 'desmoid tumor', 'desmoid type fibromatosis']",0080366,135290,873,CN072436,"['-0.002224', '0.00441', '0.004055', '0.008835', '0.01554', '-0.02118', '-0.001484', '0.006138', '-0.0176', '-0.001782', '-0.00815', '0.002607', '0.006275', '0.00486', '-0.004837', '0.0004287', '0.001913', '-0.008934', '-0.003595', '-0.01547', '0.004597', '-0.00507', '0.00138', '-0.01505', '0.0104', '0.0006747', '0.002356', '-0.005287', '-0.008865', '-0.01153', '0.01144', '0.00643', '0.02167', '0.00938', '-0.00607', '-0.01064', '-0.0117', '0.007195', '-0.001685', '-0.009346', '0.00859', '-0.00889', '0.01054', '-0.01636', '0.013084', '-0.002394', '0.00826', '0.00311', '0.0183', '0.01298', '8.91e-05', '-0.00889', '-0.001694', '-0.0026', '-0.01689', '-0.0001521', '0.010956', '-0.00808', '-0.01391', '0.00291', '0.00919', '-0.000316', '0.00203', '0.00231', '0.003014', '0.01212', '0.01982', '0.009865', '-0.01851', '0.02261', '0.00486', '0.00593', '-0.001082', '-0.003305', '-0.000628', '0.01581', '-0.00817', '-0.003508', '-0.006306', '-0.022', '-0.01953', '0.007042', '-0.002586', '0.01607', '-0.008545', '0.002598', '0.002378', '0.01657', '0.01736', '0.00833', '-0.004707', '-0.0008583', '0.003502', '0.005596', '0.02477', '0.00852', '0.013084', '-0.00448', '-0.001132', '-0.002827']",C9182,,,,,,
mondo:0007609,"fibromatosis, gingival, 1","['HGF1', 'gingival fibromatosis caused by mutation in SOS1', 'fibromatosis gingival, hereditary, 1', 'GINGF1', 'GINGF', 'fibromatosis, gingival, hereditary', 'gingival fibromatosis, 1', 'GGF1', 'fibromatosis, gingival, type 1', 'SOS1 gingival fibromatosis', 'hereditary gingival fibromatosis, 1', 'fibromatosis, gingival, 1', 'SOS1 hereditary gingival fibromatosis']",,135300,,CN030594,,,,,,,,
mondo:0007610,gingival fibromatosis-hypertrichosis syndrome,"['extreme hirsutism with gingival fibromatosis', 'congenital generalised hypertrichosis terminalis', 'hypertrichosis, congenital generalized, with gingival hyperplasia', 'chromosome 17Q24.2-q24.3 Duplication syndrome', 'microdeletion 17Q24.2-q24.3 syndrome', 'chromosome 17Q24.2-q24.3 deletion syndrome', 'hypertrichosis terminalis, generalized, with gingival hyperplasia', 'hypertrichosis terminalis, generalized, with or without gingival hyperplasia', 'congenital generalized hypertrichosis terminalis', 'hereditary gingival fibromatosis with hypertrichosis', 'hirsutism-congenital gingival hyperplasia syndrome', 'CGHT', 'fibromatosis, gingival, with hypertrichosis', 'microduplication 17Q24.2-q24.3 syndrome', 'gingival fibromatosis with hypertrichosis', 'HTC3', 'hypertrichosis with or without gingival hyperplasia', 'hypertrichosis, congenital generalized, with or without gingival hyperplasia']",,135400,2026,,,,,C565016,,,,
mondo:0007612,gingival fibromatosis-progressive deafness syndrome,"['gingival fibromatosis with sensorineural hearing loss', 'GFD', 'fibromatosis, gingival, with progressive deafness', 'Jones syndrome', 'familial gingival fibromatosis associated with progressive deafness', 'gingival fibromatosis with progressive deafness']",,135550,2027,C1851112,,,,C535886,,,,
mondo:0007614,congenital fibrosis of extraocular muscles,"['ophthalmoplegia, congenital', 'congenital fibrosis of the extraocular muscles', 'fibrosis of extraocular muscles, congenital, 1', 'Feom1 locus', 'fibrosis of extraocular muscles, congenital', 'blepharoptosis with absent eye movements', 'Tukel syndrome', 'fibrosis of extraocular muscles, congenital, 3B', 'fibrosis of extraocular muscles, congenital, type 1', 'FEOM', 'CFEOM1']",0080143,,45358,CN043677,"['-0.2683', '-0.1277', '0.1613', '-0.3677', '-0.2979', '-0.1912', '0.2455', '0.2878', '-0.8926', '0.1094', '0.1276', '0.01508', '0.03653', '0.0924', '0.1521', '-0.04675', '0.3457', '-0.2927', '0.0865', '-0.737', '-0.0229', '0.2207', '0.010895', '-0.1042', '0.0755', '-0.136', '-0.11255', '-0.1448', '0.1643', '0.1434', '-0.08215', '0.10266', '0.3367', '0.2295', '0.07947', '-0.1892', '-0.1938', '-0.2064', '-0.0963', '-0.2365', '0.337', '0.02446', '0.011566', '0.1527', '0.10364', '-0.2158', '0.08606', '0.2219', '-0.09357', '0.382', '-0.253', '0.2367', '0.1562', '-0.3743', '-0.231', '-0.1359', '0.455', '-0.08655', '-0.001575', '-0.1158', '0.4187', '-0.1987', '0.02129', '0.3542', '-0.7236', '-0.1327', '0.1255', '0.613', '-0.0942', '0.0683', '-0.2795', '0.414', '0.04272', '-0.11536', '0.2856', '0.0818', '0.335', '-0.2708', '-0.361', '-0.2222', '0.012', '-0.452', '0.1284', '0.652', '-0.4978', '-0.05246', '-0.0806', '0.1743', '0.1396', '0.11975', '0.2603', '0.4043', '0.0373', '0.1351', '0.5835', '0.05167', '0.3362', '0.08563', '0.1744', '0.1721']",,,,728.2,,,
mondo:0007615,laurin-Sandrow syndrome,"['laurin-Sandrow syndrome', 'Sandrow syndrome', 'mirror-Image polydactyly', 'fibula ulna duplication tibia radius absence', 'laurin-Sandrow syndrome, segmental', 'tetramelic mirror-Image polydactyly', 'fibula and ulna, Duplication of, with absence of tibia and radius', 'laurin Sandrow syndrome', 'LSS', 'mirror hands and feets-nasal defects syndrome', 'mirror hands and feet with nasal defects']",0111350,135750,2378,,"['-0.147', '-0.08606', '-0.07635', '0.383', '0.03568', '-0.2825', '0.2412', '0.10535', '-0.292', '-0.787', '-0.6143', '-0.334', '-0.194', '0.3154', '-0.1218', '0.2334', '0.4387', '-0.2644', '0.04004', '-0.3843', '0.0518', '0.4624', '0.253', '0.07526', '0.299', '0.4153', '-0.374', '0.3755', '0.3853', '0.3064', '0.4067', '-0.6763', '-0.3516', '0.2057', '0.6562', '-0.2198', '-0.0725', '-0.245', '-0.1494', '-0.1627', '-0.06964', '0.006367', '-0.4949', '-0.1522', '0.2385', '0.001198', '-0.2404', '0.4', '-0.3289', '-0.0742', '-0.03038', '-0.2422', '-0.1854', '0.0391', '-0.4995', '-0.1135', '0.368', '-0.0947', '-0.3386', '0.1818', '0.1465', '0.2524', '0.05618', '0.05652', '-0.3965', '-0.1209', '0.1752', '0.1609', '-0.3394', '0.4158', '-0.1718', '0.11975', '0.222', '-0.1588', '-0.04117', '0.629', '-0.1945', '-0.1964', '-0.3018', '-0.583', '0.03427', '0.0587', '0.5903', '0.658', '0.2917', '0.01863', '-0.4194', '0.7183', '0.06128', '0.004356', '-0.1766', '0.2769', '0.1355', '-0.1342', '0.839', '-0.3352', '0.2844', '-1.373', '0.1827', '-0.07306']",,,C535689,,,,
mondo:0007616,"fibula, recurrent dislocation of head of","['fibula, recurrent dislocation of head of']",,135800,,C1851099,,,,C565011,,,,
mondo:0007617,Coffin-Siris syndrome 1,"['autosomal dominant mental retardation 12', 'CSS1', 'intellectual disability, autosomal dominant 12', 'mental retardation, autosomal dominant 12', 'MRD12', 'fifth digit syndrome', 'COFFIN-SIRIS syndrome 1', 'hypertrichosis, hyperkeratosis, intellectual disability, and distinctive facial features', 'CSS', 'COFFIN-SIRIS syndrome', 'hypertrichosis, hyperkeratosis, mental retardation, and distinctive facial features', 'ARID1B-related BAFopathy', 'mental retardation, autosomal dominant type 12']",0070042,614562,,CN029606,,,,C538391,,,,
mondo:0007618,Eng-Strom syndrome,"['finger locking, recurrent, with intrauterine growth retardation and proportionate short stature', 'short stature-locking fingers syndrome']",,135950,1937,C2931545,,,,,,,,
mondo:0007619,isolated congenital adermatoglyphia,"['adermatoglyphia', 'ADG', 'absence of fingerprints', 'ADERM', 'fingerprints, absence of', 'immigration delay disease', 'isolated congenital adermatoglyphia', 'congenital absence of fingerprints']",0111357,136000,289465,,"['-1.008', '-0.195', '-0.1792', '0.1531', '0.8076', '-0.3274', '-0.2262', '0.295', '-0.2847', '-0.1458', '-0.0959', '-0.525', '-0.04242', '-0.2651', '-0.416', '0.2006', '0.6177', '-0.1835', '-0.6914', '-1.087', '-0.1516', '-0.1387', '0.7124', '-0.3086', '0.1754', '0.3025', '-0.3003', '0.505', '0.01883', '-0.4612', '0.2316', '-0.1147', '-0.06494', '0.512', '0.3098', '0.1265', '-0.1057', '0.4126', '0.0969', '-0.4043', '0.2383', '0.1735', '-0.1147', '-0.2234', '0.237', '-0.588', '0.3303', '0.5093', '0.487', '0.1293', '-0.2296', '-0.05853', '0.1212', '0.4016', '-0.607', '-0.134', '0.4827', '-0.1913', '-0.5093', '-0.2742', '-0.1836', '0.245', '0.3481', '-0.09625', '-0.07776', '0.504', '0.301', '0.457', '-0.3826', '0.4924', '-0.3606', '0.1658', '0.4075', '0.4377', '0.0813', '-0.1141', '0.775', '0.03424', '-0.1298', '-0.006325', '0.04138', '-0.2323', '0.4382', '0.126', '0.1632', '-0.797', '-0.2207', '0.604', '0.3545', '0.2174', '0.1865', '-0.00476', '0.10144', '-0.2462', '0.4453', '-0.2391', '0.489', '-0.5728', '0.1846', '0.7563']",,,C565010,,,,
mondo:0007620,fish eye disease,"['fed', 'LCATA deficiency', 'alpha-lecithin:cholesterol acyltransferase deficiency', 'partial LCAT deficiency', 'alpha-lecithin cholesterol acyltransferase deficiency', 'fish eye disease', 'dyslipoproteinemic corneal dystrophy', 'fish-eye disease', 'alpha-LCAT deficiency']",,136120,79292,C0342895,"['-0.2761', '0.4038', '-0.1587', '-0.1222', '0.4995', '-0.09485', '-0.2517', '0.56', '0.194', '-0.7256', '-0.12286', '-0.58', '-0.5093', '0.114', '-0.24', '-0.393', '0.533', '0.1385', '0.2793', '-0.322', '-0.03073', '-0.2225', '0.455', '-0.06616', '0.10803', '0.38', '0.05344', '0.0433', '-0.02634', '-0.11584', '0.5605', '0.306', '0.427', '0.388', '0.015274', '-0.192', '-0.1993', '-0.731', '-0.0386', '-0.317', '0.5786', '-0.2222', '0.3806', '-0.4077', '-0.6387', '0.2329', '0.2124', '0.07745', '0.1453', '0.2137', '0.6875', '0.03262', '0.2174', '-0.113', '-0.2805', '0.02025', '0.1738', '-0.797', '-0.383', '-0.06494', '0.1376', '0.088', '0.2507', '-0.6797', '0.3594', '-0.2113', '0.5615', '0.716', '0.12427', '-0.10645', '0.401', '-0.4521', '-0.0796', '0.402', '0.5205', '0.632', '0.01607', '-0.02339', '-0.1401', '0.3162', '0.07227', '-0.1877', '-0.2837', '0.6245', '0.11005', '0.01746', '0.3088', '-0.1368', '0.7866', '0.503', '0.414', '0.816', '-0.2139', '0.473', '0.8457', '0.6143', '0.2072', '-0.1509', '-0.2585', '-0.1242']",,,,,,,
mondo:0007621,Floating-Harbor syndrome,"['FLHS', 'floating-HARBOR syndrome', 'floating-Harbor syndrome', 'Pelletier-Leisti syndrome', 'short stature with delayed bone age, expressive language delay, a triangular face with a prominent nose and deep-set eyes', 'FHS']",0111358,136140,2044,C0729582,"['0.1718', '0.2178', '0.2944', '-0.2488', '0.1179', '-0.012344', '0.4036', '1.434', '-0.8276', '-0.4644', '0.3167', '0.2217', '0.6504', '-0.02997', '0.225', '0.1169', '0.3728', '-0.4675', '-0.4092', '-0.596', '0.0948', '0.1333', '0.1602', '-0.6084', '0.412', '-0.4414', '-0.452', '0.1638', '0.4907', '-0.3665', '0.1873', '-0.1833', '0.1832', '0.365', '0.2612', '-0.11017', '0.204', '-0.2903', '-0.1626', '-0.0816', '-0.10944', '-0.3076', '-0.253', '-0.2683', '0.3467', '-0.4468', '0.2325', '0.4358', '-0.2362', '0.049', '-0.2028', '0.1661', '-0.829', '0.694', '-0.552', '-0.1964', '-0.569', '-0.0085', '0.1552', '-0.03656', '0.1458', '0.08984', '-0.4187', '-0.3608', '0.1871', '-0.006382', '0.3474', '0.4111', '-0.2678', '-0.1954', '-0.2472', '0.3013', '-0.2874', '-0.02702', '0.4175', '0.254', '0.05893', '-0.578', '-0.813', '0.11505', '0.2388', '0.04916', '-0.02164', '0.4805', '-0.239', '0.2817', '-0.4417', '0.281', '0.5713', '0.3872', '0.4446', '0.134', '0.1846', '0.231', '0.5093', '-0.3147', '0.2642', '-0.818', '0.471', '0.267']",C175241,,C537062,759.89,,,
mondo:0007623,flushing of ears and somnolence,['flushing of ears and somnolence'],,136200,,C1851055,,,,,,,,
mondo:0007624,Flynn-Aird syndrome,"['Flynn-Aird syndrome', 'Flynn Aird syndrome', 'cataracts, retinitis pigmentosa, sensorineural hearing loss, ataxia, peripheral neuritis, epilepsy, dementia, skin atrophy, chronic ulceration, dental']",,136300,2047,C0343108,,,,C537066,,,,
mondo:0007625,focal epithelial hyperplasia of the oral mucosa,['focal epithelial hyperplasia of the oral mucosa'],,136400,,C1851009,,,,C565008,,,,
mondo:0007626,familial congenital palsy of trochlear nerve,"['superior oblique oculomotor palsy, familial congenital', 'hereditary fourth cranial nerve palsy', 'strabismus from Superior oblique palsy', 'trochlear nerve palsy, familial congenital', 'fourth cranial nerve palsy, familial congenital']",,136480,91498,C1850996,,,,C565007,,,,
mondo:0007627,focal facial dermal dysplasia type I,"['FFDD type I', 'Brauer syndrome', 'hereditary symmetrical aplastic nevi of temples', 'focal facial dermal dysplasia type 1', 'bitemporal aplasia cutis congenita', 'FFDD1', 'focal facial dermal dysplasia 1, Brauer type', 'FFDD, type 1']",,136500,79133,CN776929,,,,,,,,
mondo:0007628,foveal hypoplasia 1,"['foveal hypoplasia, congenital nystagmus, corneal pannus, and presenile cataracts', 'foveal hypoplasia 1', 'foveal hypoplasia 1 with or without anterior segment anomalies and/or cataract', 'FVH1', 'foveal hypoplasia, presenile cataract', 'PAX6 foveal hypoplasia', 'foveal hypoplasia type 1', 'foveal hypoplasia caused by mutation in PAX6', 'O Donnell Pappas syndrome']",,136520,2253,C3805604,"['-0.576', '-0.0096', '-0.0845', '0.03244', '0.1951', '-0.1189', '-0.2126', '0.419', '-0.3572', '-0.4043', '-0.1517', '-0.3052', '-0.137', '-0.0799', '-0.1989', '-0.1991', '0.383', '-0.4563', '0.10455', '-0.588', '-0.00702', '-0.04504', '-0.1659', '0.2029', '0.4414', '0.2605', '-0.366', '0.3403', '0.317', '0.0675', '0.4368', '0.365', '0.3289', '0.233', '0.3137', '-0.1218', '0.1203', '-0.3792', '0.1326', '-0.2651', '0.2485', '-0.001239', '0.1311', '0.2279', '-0.1901', '-0.06964', '0.05353', '-0.0348', '0.174', '-0.2505', '0.1014', '0.2184', '-0.11847', '-0.188', '-0.1013', '0.01924', '0.736', '-0.211', '-0.3237', '0.0666', '0.2068', '0.1461', '0.07135', '0.2229', '-0.1288', '-0.0156', '0.5522', '0.748', '-0.02731', '0.4316', '-0.4072', '0.0939', '0.2069', '-0.2393', '0.32', '-0.4355', '0.3918', '0.01188', '-0.2678', '0.04858', '0.2576', '-0.04565', '0.3547', '0.629', '-0.355', '-0.3403', '0.04327', '0.65', '0.3853', '0.2366', '0.135', '0.5303', '0.1595', '0.02382', '0.5786', '-0.32', '0.568', '-0.2151', '0.171', '0.2568']",,,,,,,
mondo:0007629,fragile site 10Q23,"['fragile site type 10Q23', 'fragile site 10Q23']",,136540,,C1850987,,,,,,,,
mondo:0007630,North Carolina macular dystrophy,"['foveal dystrophy, progressive', 'North Carolina macular dystrophy', 'NCMD', 'macular dystrophy, retinal, 1, NORTH Carolina type', 'foveal dystrophy, progressive, formerly', 'macular dystrophy 1, North Carolina type', 'retinal pigment epithelial dystrophy, central', 'caped', 'macular dystrophy retinal 1 North Carolina type', 'retinal pigment epithelial dystrophy central', 'progressive foveal dystrophy', 'North Carolina macular dystrophy, retinal 1', 'MCDR1', 'central retinal pigment epithelial dystrophy', 'CAPE dystrophy', 'central areolar pigment epithelial dystrophy', 'foveal dystrophy progressive']",,136550,75327,C0730294,,,,C537835,,H35.5,,
mondo:0007631,"chromosome 16p12.1 deletion syndrome, 520kb","['fragile site, Distamycin a type, Rare, fra(16)(p12.1)', 'fragile site 16P12', 'chromosome 16p12.1 deletion syndrome', 'Recurrent 16p12.1 microdeletion (neurodevelopmental susceptibility locus)', 'chromosome 16p12.1 deletion syndrome, 520-KB', 'chromosome 16p12.1 deletion syndrome, type 520kb']",0060399,136570,,,,C129875,,C565001,,,,
mondo:0007633,"Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness","['Friedreich ataxia, so-called, with optic atrophy and sensorineural deafness']",,136600,,C1850982,,,,C564999,,,,
mondo:0007634,"intellectual disability, FRA12A type","['mental retardation, FRA12A type', 'intellectual disability, FRA12A type']",,136630,,C1969893,,,,C566980,,,,
mondo:0007635,Frasier syndrome,"['Frasier syndrome, autosomal dominant, somatic mutation', 'Frasier syndrome']",0050438,136680,347,C0950122,"['0.2527', '-0.3457', '-0.542', '-0.1475', '-0.03012', '-0.777', '0.1344', '0.611', '-0.1512', '-0.674', '-0.2002', '-0.0379', '0.2214', '0.3135', '0.2472', '-0.2964', '0.4648', '-0.3748', '0.3599', '-1.176', '-0.1417', '-0.1431', '0.2551', '-0.0834', '0.3806', '-0.1686', '0.1676', '0.4084', '0.09534', '-0.6196', '0.663', '0.1588', '0.94', '-0.613', '0.0636', '-0.6924', '-0.0814', '0.1261', '-0.4443', '-0.2156', '-0.2251', '0.3828', '-0.00359', '-0.00977', '-0.201', '0.1532', '-0.662', '-0.8633', '-0.06238', '0.3713', '0.298', '0.4563', '0.2424', '0.112', '-0.09894', '-0.10065', '0.1954', '-0.416', '-1.056', '-0.114', '0.676', '0.3096', '0.3047', '0.4773', '0.1384', '0.2025', '0.1589', '0.614', '-0.3074', '0.1155', '-0.307', '-0.03415', '-0.133', '0.319', '0.501', '-0.5044', '0.2008', '0.6245', '-0.697', '0.2075', '0.22', '0.944', '0.11505', '0.5796', '-0.3296', '-0.3528', '-0.1829', '-0.1283', '-0.03069', '0.359', '-0.1549', '0.777', '-0.8276', '0.01878', '0.0846', '-0.6416', '0.1979', '-0.4988', '-0.2239', '0.1169']",C122805,,D052159,759.89,,,
mondo:0007636,frontorhiny,"['frontonasal dysplasia type 1', 'frontonasal malformation', 'FND1', 'isolated median cleft syndrome', 'frontonasal dysplasia 1', 'frontonasal dysplasia', 'frontorhiny', 'ALX3-related frontonasal dysplasia', 'median Facial cleft syndrome', 'isolated median cleft face syndrome']",0081045,136760,391474,,"['-0.09424', '0.2747', '0.1477', '-0.5005', '0.2369', '-0.0636', '-0.1382', '0.2091', '-0.602', '-0.266', '-0.2429', '-0.3264', '0.2725', '-0.3618', '-0.2883', '0.2678', '0.2593', '-0.1423', '-0.113', '-0.1975', '-0.04837', '-0.047', '0.2316', '-0.06506', '0.3242', '0.05045', '-0.2174', '0.1658', '0.424', '-0.3806', '0.3809', '0.1754', '-0.0377', '-0.0834', '0.1641', '-0.0881', '0.0787', '0.00586', '0.08246', '-0.755', '0.2335', '-0.1849', '0.097', '-0.1214', '-0.1427', '-0.6704', '0.2551', '0.36', '0.1742', '-0.289', '-0.0455', '-0.326', '-0.544', '0.2446', '-0.3767', '-0.651', '0.2747', '0.08527', '-0.3186', '0.4053', '0.0918', '0.1284', '-0.3464', '0.179', '0.05096', '-0.1332', '0.1434', '0.09937', '-0.1626', '0.4014', '-0.4822', '0.1934', '0.2515', '0.085', '-0.04672', '0.4197', '0.0701', '0.02173', '-0.2446', '-0.1885', '0.2502', '0.04633', '-0.0794', '0.6123', '-0.10236', '0.2703', '-0.2805', '0.429', '0.002827', '0.1876', '-0.4614', '0.445', '0.2136', '-0.0602', '0.8687', '-0.11536', '0.2493', '-0.4856', '0.09863', '-0.05286']",C129028,,,,,,
mondo:0007637,"corneal dystrophy, Fuchs endothelial, 1","['corneal dystrophy, Fuchs endothelial, 1', 'corneal dystrophy, Fuchs endothelial, type 1', 'Fuchs^ endothelial dystrophy caused by mutation in COL8A2', 'COL8A2 Fuchs^ endothelial dystrophy', 'FECD1', 'corneal dystrophy, Fuchs endothelial, early-onset']",,136800,,C1850959,,,,C535478,,,,
mondo:0007638,fucosidase regulator,"['Alpha-L-fucosidase regulator', 'fucosidase regulator']",,136830,,,,,,,,,,
mondo:0007639,fundus albipunctatus,"['fundus albipunctatus', 'pigmentary retinal dystrophy', 'retinitis punctata albescens']",11105,136880,227796,,"['-0.6606', '-0.09875', '-0.7207', '0.281', '0.0392', '-0.397', '0.0852', '0.1754', '-0.358', '-0.4436', '0.03717', '-0.2162', '-0.277', '0.4636', '0.2505', '-0.04993', '0.4827', '-0.3174', '-0.3022', '-0.9546', '-0.03053', '0.1561', '0.413', '0.584', '-0.462', '0.1711', '-0.02985', '-0.2783', '-0.3123', '0.518', '0.988', '-0.317', '-0.1207', '0.6963', '0.0737', '0.589', '0.03915', '-0.1443', '-0.0608', '-0.3774', '0.7725', '-0.2013', '0.05768', '0.1976', '-0.721', '-0.2335', '0.05054', '-0.2325', '0.71', '0.619', '0.593', '-0.0575', '0.197', '-0.1486', '-0.1791', '0.262', '1.094', '-0.3052', '-0.424', '-0.26', '0.2808', '-0.2522', '-0.0224', '0.03134', '-0.2866', '0.2109', '0.776', '1.095', '-0.0217', '0.7695', '0.0907', '-0.003775', '0.1576', '0.1572', '0.1495', '-0.08844', '-0.001403', '0.0485', '-0.2308', '-0.4092', '-0.184', '0.01548', '0.314', '0.693', '-0.09344', '-0.2625', '-0.339', '0.08594', '0.4006', '-0.2117', '0.1694', '0.5586', '-0.2966', '0.2133', '-0.001457', '-0.166', '0.2091', '-0.523', '0.0541', '0.3564']",,,C562733,362.76,H35.5,,
mondo:0007640,Sorsby fundus dystrophy,"['Sorsby pseudoinflammatory fundus dystrophy', 'hemorrhagic macular dystrophy', 'Sorsby fundus dystrophy', 'fundus dystrophy, pseudoinflammatory, of Sorsby', 'SFD', 'pseudoinflammatory fundus dystrophy of Sorsby', 'macular dystrophy, hemorrhagic', 'Sorsby^s pseudoinflammatory macular dystrophy', 'Sorsby^s fundus dystrophy']",0090114,136900,59181,,"['-0.1587', '0.1472', '0.01088', '0.1186', '0.2128', '-0.4304', '-0.05847', '0.2393', '-0.3208', '-0.07434', '-4.905e-05', '-0.05075', '-0.2043', '-0.11755', '0.05685', '-0.5337', '0.1494', '-0.1349', '0.1304', '-0.5596', '-0.378', '-0.1436', '-0.2023', '0.368', '-0.05447', '0.0425', '-0.05496', '-0.1254', '-0.3176', '0.267', '0.3245', '-0.02412', '0.0712', '0.0552', '-0.02168', '0.3179', '0.1831', '-0.01328', '-0.06506', '-0.2825', '0.1799', '-0.1805', '0.2385', '0.0795', '-0.2157', '0.0816', '-0.148', '-0.1288', '0.02011', '0.1543', '0.3418', '0.2795', '0.08984', '-0.2312', '0.1262', '-0.3828', '0.4517', '0.1068', '-0.545', '-0.08234', '0.151', '-0.1135', '0.2051', '0.387', '-0.04715', '-0.0659', '0.552', '0.5366', '-0.2278', '0.38', '-0.3025', '0.02321', '0.322', '-0.3062', '0.399', '0.0392', '-0.1758', '0.0692', '-0.151', '-0.1964', '0.2678', '-0.23', '-0.0659', '0.591', '-0.1683', '-0.2307', '0.11646', '0.008865', '0.2056', '0.1469', '0.2158', '0.2399', '0.12427', '0.3247', '0.4146', '-0.03836', '0.4558', '-0.2006', '-0.01381', '0.3074']",,,C564992,,,,
mondo:0007642,isolated agenesis of gallbladder,"['gallbladder, agenesis OF']",,137040,440987,,,,,C562564,,,,
mondo:0007643,"gamma-A-globulin, defect in assembly of","['gamma-A-globulin, defect in ASSEMBLY OF', 'IgA, defect in Assembly of', 'Immunoglobulin A, defect in Assembly of']",,137050,,C1850934,,,,C564991,,,,
mondo:0007644,IgAD1,"['IMMUNOGLOBULIN A deficiency 1', 'Immunoglobulin A, selective deficiency of', 'immunoglobulin A deficiency, autosomal recessive, autosomal dominant, isolated cases', 'IgAD1', 'gamma-A-globulin, selective deficiency of', 'IgA, selective deficiency of']",,137100,,,,C123434,,C536290,,,,
mondo:0007646,Gamstorp-Wohlfart syndrome,"['autosomal recessive Charcot-Marie-Tooth disease type 2 with neuromyotonia', 'ARAN-NM', 'neuromyotonia and axonal neuropathy, autosomal recessive', 'NMAN', 'myokymia, myotonia, and muscle wasting', 'autosomal recessive neuromyotonia and axonal neuropathy', 'ARCMT2-NM', 'myokymia, myotonia and muscle wasting', 'Gamstorp-Wohlfart syndrome', 'autosomal recessive axonal neuropathy with neuromyotonia']",0050526,137200,324442,CN074193,"['-0.845', '0.01247', '0.569', '-0.376', '0.304', '-0.709', '0.235', '0.4158', '-0.536', '0.273', '0.02501', '0.5117', '0.11145', '-0.3833', '0.2125', '0.586', '0.1168', '-0.4565', '-0.3635', '-0.7695', '0.3162', '-0.02141', '0.3462', '0.7817', '-0.3225', '0.0597', '0.386', '-0.3286', '-0.9053', '-0.04318', '-0.02705', '0.03323', '0.3552', '0.4053', '0.01041', '-0.3767', '-0.633', '-0.5137', '-0.02257', '-0.612', '-0.5825', '-0.5664', '0.04303', '0.627', '0.04202', '-0.4841', '-0.4607', '0.4583', '-0.1292', '0.4932', '-0.2776', '0.4402', '-0.1417', '-0.5024', '-0.3315', '-0.3208', '0.1484', '-0.2874', '-0.612', '-0.11456', '-0.2047', '0.03638', '0.2354', '0.3953', '-0.7207', '0.424', '0.1365', '0.7246', '-0.1967', '-0.04114', '-0.11676', '0.2216', '0.285', '-0.3845', '1.0', '0.3438', '0.1945', '0.6016', '0.2915', '-0.4685', '-0.1884', '-0.3198', '0.735', '0.7744', '0.339', '0.2888', '-0.379', '0.4912', '-0.06915', '-0.2028', '0.78', '0.013596', '0.317', '0.2576', '0.707', '0.5396', '0.3706', '-0.3865', '-0.293', '0.3599']",,,,,,,
mondo:0007647,"gastric volvulus, intrathoracic","['gastric volvulus, intrathoracic']",,137210,,C1850902,,,,C564989,,,,
mondo:0007648,hereditary diffuse gastric adenocarcinoma,"['FDGC', 'signet cell adenocarcinoma', 'hereditary diffuse gastric cancer', 'diffuse gastric cancer', 'hereditary diffuse cancer of stomach', 'HDGC', 'familial diffuse gastric cancer', 'familial diffuse cancer of stomach', 'signet ring cell gastric carcinoma', 'signet ring gastric carcinoma', 'hereditary diffuse gastric adenocarcinoma']",0080764,,26106,C1708349,"['-0.02246', '0.0403', '0.0067', '-0.033', '-0.02249', '-0.067', '0.006283', '0.0635', '-0.0553', '0.01111', '-0.01049', '0.00251', '-0.02231', '0.00333', '-0.03516', '-0.0483', '0.00434', '-0.04526', '0.009155', '-0.127', '-0.000452', '-0.05017', '0.0633', '-0.0266', '0.04062', '-0.00921', '0.01304', '-0.010414', '-0.00113', '-0.06586', '0.05582', '-0.00481', '0.06885', '-0.008675', '0.03195', '-0.04352', '-0.04068', '-0.034', '0.0009246', '-0.06064', '0.02025', '-0.0983', '0.02649', '-0.04272', '0.00325', '-0.04944', '-0.0403', '0.02638', '0.01628', '0.03772', '-0.006405', '0.00854', '0.008965', '0.005333', '-0.06116', '-0.01158', '0.0909', '-0.00959', '-0.1277', '0.002668', '0.04745', '0.0334', '0.00629', '0.00791', '-0.0009604', '0.02635', '0.11206', '0.10187', '-0.06168', '0.10767', '-0.04614', '0.0311', '0.03026', '-0.05338', '0.06604', '0.02388', '0.002192', '-0.01762', '-0.03204', '-0.03123', '-0.04', '0.03162', '-0.01151', '0.05066', '-0.07074', '-0.00927', '0.02034', '0.04996', '0.0742', '-0.01598', '0.05508', '0.0798', '0.02602', '0.0257', '0.1448', '0.00798', '0.0935', '-0.0841', '-0.03516', '0.03336']",C43295,,,,,,
mondo:0007650,MALT lymphoma,"['gastric lymphoma, primary', 'extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue (MALT lymphoma)', 'MALT lymphoma', 'mucosa-associated lymphoid tissue lymphoma', 'Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue', 'Immunocytoma', 'lymphoma of mucosa-associated lymphoid tissue', 'lymphoma, mucosa-associated lymphoid type', 'Extranodal marginal zone B-cell lymphoma of mucosa-associated lymphoid tissue (MALT-lymphoma)', 'Extranodal marginal zone lymphoma of mucosa-associated lymphoid tissue', 'Extranodal marginal zone B-cell lymphoma', 'lymphoma, MALT, somatic', 'MALToma', 'MALT-lymphoma', 'familial primary gastric lymphoma', 'mucosa-associated lymphatic tissue lymphoma']",0050909,137245,52417,C1850900,"['-0.06726', '0.1116', '0.1555', '-0.689', '0.1368', '0.04578', '0.6543', '1.14', '-0.495', '-0.4387', '0.5757', '0.298', '-1.165', '0.4211', '-0.2064', '0.196', '-0.748', '-0.4775', '-0.6064', '-0.2302', '-0.2427', '-0.3477', '0.391', '-0.3044', '0.325', '0.293', '-0.001392', '-0.01135', '-0.1558', '-0.669', '0.558', '0.6396', '0.7837', '-0.2961', '0.3875', '0.2347', '-1.356', '0.2905', '0.02553', '-0.03873', '0.2964', '-0.07544', '0.2427', '-0.6025', '0.1328', '0.5063', '-0.919', '-0.4485', '0.689', '0.01787', '-0.11176', '-0.05945', '0.254', '-0.1715', '-0.8994', '0.7134', '-0.0842', '0.01', '-0.2932', '-0.481', '0.4482', '0.008484', '0.11835', '-0.1451', '0.1366', '-0.08075', '0.3057', '0.428', '0.1019', '1.314', '-0.0314', '0.1348', '-0.3845', '-0.467', '0.582', '-0.1417', '0.00471', '0.4807', '-0.1628', '-0.29', '-0.74', '-0.4062', '0.2072', '-0.12225', '-0.4214', '-0.3591', '0.293', '-0.10767', '0.4426', '-0.093', '0.3206', '-0.2551', '0.1783', '-0.4014', '1.105', '0.436', '-0.5845', '0.214', '-0.2157', '-0.0163']",C3898,0000191,,202.80,,10060707,
mondo:0007651,gastrocutaneous syndrome,"['peptic Ulcer/hiatal hernia, multiple lentigines/cafe-Au-lait Spots, hypertelorism, myopia', 'gastrocutaneous syndrome']",,137270,2069,C1850899,,,,C535651,,,,
mondo:0007652,gastric mucosal hypertrophy,"['gastritis, familial giant hypertrophic', 'familial giant hypertrophic gastritis', 'giant hypertrophic gastritis', 'Menetrier^s disease', 'Menetrier disease', 'hypertrophic gastropathy', 'giant hypertrophic gastropathy', 'Gastroenteropathy, protein losing', 'giant rugal hypertrophy of stomach', 'hypertrophic gastritis', 'giant hypertrophy of the gastric mucosa', 'MENETRIER disease', 'Ménétrier disease', 'hypoproteinemic hypertrophic gastropathy']",8757,137280,2494,C0017155,,C67277,1000946,D005758,535.21,,10017868,
mondo:0007653,genochondromatosis,['genochondromatosis'],,137360,,C1300229,,,,C563215,,,,
mondo:0007654,"genu valgum, st. Helena familial","['severe ^knock-knees^ and variable lesser malalignment at the elbows and wrists', 'genu valgum, st. Helena familial', 'genu valgum, hereditary pubertal', 'genu valgum, st Helena familial', 'St. Helena familial genu valgum', 'hereditary pubertal genu valgum']",,137370,,C1842052,,,,C537685,,,,
mondo:0007655,fissured tongue,"['tongue, fissured', 'lingua plicata', 'erythema migrans', 'glossitis, benign migratory', 'geographic tongue and fissured tongue', 'scrotal tongue', 'geographic and fissured tongue', 'fissure of tongue', 'congenital plicated tongue', 'fissure of tongue, congenital', 'plicated tongue', 'congenital fissure of tongue', 'Furrowed tongue', 'ectopic geographic tongue']",11514,137400,,C1842051,,,,D014063,750.13,K14.5,,
mondo:0007656,Gerstmann-Straussler-Scheinker syndrome,"['encephalopathy subacute spongiform Gerstmann-Straussler type', 'Gerstmann-Straussler-Scheinker disease', 'amyloidosis cerebral with spongiform encephalopathy', 'cerebellar ataxia, progressive dementia, and amyloid deposits in the central nervous system', 'amyloidosis, cerebral, with spongiform encephalopathy', 'GSD', 'Gerstmann-Straussler disease', 'Gerstmann Straussler Scheinker syndrome', 'prion dementia', 'cerebellar ataxia, progressive dementia, and amyloid deposits in CNS', 'cerebral amyloid angiopathy, Prnp-related', 'encephalopathy, Subacute spongiform, Gerstmann-Straussler type', 'subacute spongiform encephalopathy, Gerstmann-Straussler type']",4249,137440,356,C0017495,"['0.2412', '0.5356', '-0.4778', '0.003857', '-0.4126', '-1.047', '-0.3525', '-0.06073', '-0.3264', '0.261', '-0.4526', '-0.4502', '-0.399', '-0.2479', '0.7124', '0.02815', '-0.288', '-0.855', '-0.09674', '-0.371', '0.3271', '-0.416', '-0.202', '0.1394', '0.558', '0.2021', '-0.4446', '0.03326', '-0.2308', '-0.5044', '0.713', '-0.5293', '0.1841', '-0.0897', '0.2303', '-0.5337', '0.01034', '0.3865', '-0.784', '0.05475', '0.1649', '-0.3918', '-0.01936', '-0.06076', '0.727', '0.1902', '0.08215', '-0.2314', '-0.07983', '-0.01148', '0.1421', '0.2925', '-0.4722', '-0.2834', '0.35', '-0.514', '0.831', '-0.2074', '-0.0426', '0.567', '-0.099', '0.641', '0.4373', '-0.0504', '-0.001623', '0.075', '0.3616', '0.1779', '-0.3467', '0.753', '-0.1812', '0.26', '0.2231', '0.1587', '0.1548', '0.8774', '0.2242', '0.4922', '-0.3333', '-0.7324', '0.01608', '-0.764', '-0.2145', '0.5303', '0.2202', '-0.1758', '0.545', '0.4211', '0.7217', '-0.05865', '-0.1533', '-0.1288', '-0.341', '-0.07196', '0.4575', '0.12384', '0.274', '-0.0259', '-0.09436', '-0.2296']",C84727,,C535800,046.71,A81.82,10072075,
mondo:0007657,giant neutrophil leukocytes,['giant neutrophil leukocytes'],,137500,,C1842039,,,,,,,,
mondo:0007660,familial ossifying fibroma,"['cemental dysplasia, periapical', 'Cementomas, familial multiple', 'GIGANTIFORM cementoma, familial', 'multiple ossifying fibroma', 'Jaffe-Campanacci syndrome', 'hereditary ossifying fibroma (disease)', 'intracortical fibrous dysplasia']",,137575,435329,CN237560,,,,C563017,,,,
mondo:0007661,Tourette syndrome,"['Guinon^s disease', 'Tourette disease', 'chronic motor tics', 'Gilles de la Tourette syndrome', 'Tourette disorder', 'psychogenic tics', 'motor-verbal tic disorder', 'Tourette syndrome', 'GTS', 'Gilles De 50A Tourette syndrome', 'Tourette^s syndrome']",11119,137580,856,,"['0.3433', '0.328', '0.001385', '0.2864', '-0.2091', '-0.2744', '0.6294', '-0.11896', '-0.4082', '-0.3247', '0.5806', '-0.2242', '0.02368', '0.907', '0.511', '-0.1627', '-0.699', '-0.288', '-0.262', '-0.618', '-0.2323', '0.1359', '-0.1584', '-0.3147', '-0.01685', '-0.4705', '-0.1313', '-0.0846', '0.4539', '-0.4207', '-0.331', '-0.03622', '0.6797', '0.5034', '0.052', '0.4915', '-0.2218', '-0.2744', '0.0747', '-0.53', '0.512', '-0.4082', '-0.344', '0.02559', '0.5225', '-0.6836', '-0.4363', '0.3608', '-0.1661', '0.971', '-0.483', '0.1094', '-0.269', '0.2537', '0.283', '0.3164', '-0.7397', '0.506', '0.0521', '-0.3054', '-0.07355', '0.12115', '0.4902', '0.3489', '-0.5195', '-0.0901', '0.47', '0.992', '-0.01409', '0.445', '0.2386', '-0.1382', '0.11786', '-0.1653', '0.4666', '0.7583', '0.03613', '1.096', '0.1272', '-0.01633', '0.6104', '-0.2883', '-0.1952', '0.1109', '0.4004', '-0.0061', '-0.000686', '0.2917', '0.9487', '0.727', '-0.1418', '0.05377', '-0.474', '-0.00829', '0.06775', '-0.4053', '0.2617', '-0.815', '0.002306', '0.37']",C35078,0004895,D005879,307.23,,,
mondo:0007662,anterior segment dysgenesis 4,"['iridogoniodysgenesis caused by mutation in PITX2', 'iris hypoplasia with early-onset glaucoma, autosomal dominant', 'iridogoniodysgenesis type 2', 'anterior segment dysgenesis 4', 'PITX2 iridogoniodysgenesis', 'IRID2', 'iridogoniodysgenesis, type 2', 'iridogoniodysgenesis syndrome', 'ASGD4']",0080609,137600,,C1842031,,,,,,,,
mondo:0007663,glaucoma with elevated episcleral venous pressure,['glaucoma with elevated episcleral venous pressure'],,137700,,C1842030,,,,C564235,,,,
mondo:0007664,"glaucoma 1, open angle, A","['JOAG1A', 'glaucoma hereditary, juvenile', 'GLC1A', 'primary open angle glaucoma juvenile onset 1', 'MYOC juvenile open angle glaucoma', 'glaucoma 1, open angle, 50', 'JOAG1', 'MYOC juvenile glaucoma', 'glaucoma, primary open angle, juvenile-onset, 1', 'glaucoma 1, open angle, type A', 'glaucoma 1A, primary open angle', 'juvenile glaucoma caused by mutation in MYOC', 'glaucoma 1, open angle, A']",,137750,,C1842028,,,,C564234,,,,
mondo:0007666,glaucoma-sleep apnea syndrome,"['glaucoma and sleep apnea', 'glaucoma sleep apnea']",,137763,2085,C1842025,,,,C564232,,,,
mondo:0007667,subependymoma,"['subependymal astrocytoma (formerly)', 'SUBEPENDYMOMA, benign', 'WHO grade I ependymal tumor', 'mixed subependymoma-ependymoma', 'WHO grade I ependymal tumour', 'subependymoma', 'WHO grade I ependymal neoplasm', 'subependymal glioma', 'subependymal astrocytoma']",4843,,251639,C0206725,,C3795,1001197,D018315,,,,
mondo:0007668,globulin anomaly involving beta (2A)-globulin,['globulin anomaly involving beta (2A)-globulin'],,137900,,C1842009,,,,C564229,,,,
mondo:0007669,renal cysts and diabetes syndrome,"['HNF1B-MODY', 'FJHN, atypical', 'maturity-onset diabetes of the young type 5', 'familial hypoplastic glomerulocystic kidney', 'glomerulocystic kidney, familial hypoplastic', 'maturity-onset diabetes of the Young, type 5', 'hypoplastic type glomerulocystic kidney disease', 'RCAD syndrome', 'renal cysts and diabetes syndrome', 'maturity onset diabetes of the Young, type 5', 'glomerulocystic kidney disease, hypoplastic type', 'hepatocyte nuclear Factor 1-beta-associated monogenic diabetes', 'atypical FJHN', 'congenital anomalies of the kidney and urinary tract with diabetes', 'CAKUT with diabetes', 'RCAD', 'HNF1B-related renal cysts and diabetes syndrome', 'FJHN atypical', 'hyperuricemic nephropathy, familial juvenile, atypical', 'renal dysfunction-early-onset diabetes syndrome', 'MODY5', 'atypical familial juvenile hyperuricemic nephropathy', 'MODY type 5', 'renal cysts-maturity-onset diabetes of the young syndrome']",0111101,137920,93111,CN206512,"['0.756', '-0.11835', '0.2844', '0.874', '-0.4204', '-0.694', '-0.3223', '0.9893', '-0.1073', '-0.646', '-0.05945', '-0.432', '0.1252', '0.0729', '-1.086', '-0.4092', '0.2832', '0.03738', '0.01003', '-0.7373', '0.3496', '-0.10956', '0.1367', '0.1637', '-0.622', '-0.3608', '0.026', '0.0356', '0.6396', '-0.4211', '0.777', '-0.3804', '0.2993', '-0.3218', '0.0957', '0.4905', '-0.8013', '0.585', '0.04706', '-0.09204', '0.1577', '0.5034', '0.388', '0.2773', '-0.3083', '-0.357', '0.307', '-0.3176', '0.182', '-0.0793', '0.12213', '-0.2083', '0.764', '-0.7383', '-0.1676', '0.2556', '-0.01929', '-0.749', '-1.189', '0.654', '-0.3535', '0.603', '-0.2186', '0.1696', '-0.09564', '0.6206', '-0.472', '0.5693', '-0.736', '-0.1973', '0.0884', '0.247', '0.3516', '0.04376', '0.5713', '0.2456', '-0.5464', '0.98', '-0.433', '-0.1257', '0.2047', '0.0636', '0.2307', '-0.718', '0.286', '0.1796', '0.185', '0.5967', '0.8755', '0.1527', '0.709', '0.56', '-0.0669', '-0.2108', '1.334', '0.1527', '0.03253', '-0.1958', '-0.286', '0.4724']",C123018,,C535520,,,,
mondo:0007670,hypotrichosis-lymphedema-telangiectasia syndrome (grouping),['hypotrichosis lymphedema telangiectasia syndrome'],,,69735,,"['0.619', '-0.0751', '-0.4163', '-0.0379', '-0.1191', '-1.235', '0.4836', '0.1876', '-0.02954', '-0.567', '0.351', '1.503', '0.01022', '1.026', '-0.413', '0.0927', '-0.06866', '-0.2815', '-0.4307', '-0.372', '0.01005', '0.0923', '0.01404', '0.2035', '0.1116', '0.08325', '-0.4238', '0.8403', '0.4534', '-0.0663', '-0.605', '0.4246', '0.5483', '-0.2708', '0.2964', '0.3376', '-0.3733', '-0.0977', '0.7944', '-0.592', '0.11176', '0.274', '0.4248', '0.007427', '0.2363', '-0.15', '-0.557', '-0.935', '1.163', '-0.6167', '-0.0406', '-0.3513', '0.752', '0.418', '-0.75', '-0.1033', '0.08044', '-1.09', '-1.06', '-0.629', '0.202', '0.3584', '-0.3616', '-0.146', '-0.512', '0.6733', '0.5337', '1.033', '-0.672', '-0.1105', '-0.8438', '0.159', '-0.06647', '-0.3337', '0.4756', '0.1924', '-0.601', '0.763', '0.1652', '-0.11914', '-0.3525', '0.6543', '-0.287', '0.5894', '0.814', '-0.2372', '-0.617', '-0.5127', '-0.1017', '0.009796', '0.0484', '0.961', '-0.4155', '0.2954', '1.363', '0.2418', '0.8936', '-0.381', '0.132', '-0.07916']",,,,,,,
mondo:0007671,fibronectin glomerulopathy,"['GFND2', 'lobular glomerulopathy, familial', 'glomerulopathy with fibronectin deposits 1', 'GFND', 'glomerulopathy with fibronectin deposits', 'fibronectin glomerulopathy', 'GFND1', 'glomerular nephritis, familial, with fibronectin deposits', 'glomerulopathy with fibronectin deposits 2', 'glomerulopathy with giant fibrillar deposits']",,,84090,,"['0.2184', '-0.0653', '-0.593', '0.69', '-0.443', '-0.7197', '-0.3933', '0.509', '-0.889', '-0.2307', '-0.07513', '-0.1849', '-0.0327', '0.2957', '-0.275', '0.3716', '0.1356', '-0.415', '0.543', '-0.353', '-0.0879', '-0.2063', '0.3953', '0.01587', '0.7744', '-0.1454', '0.04797', '0.784', '0.02235', '0.2837', '1.24', '-0.06113', '0.6084', '0.154', '0.1259', '-0.7417', '-0.07825', '0.307', '-0.0167', '0.509', '-0.1456', '0.00693', '0.665', '-0.1815', '0.07214', '-0.4106', '-0.5005', '-0.3047', '-0.2058', '-0.3281', '-0.078', '0.2815', '0.365', '-0.3567', '0.2993', '-0.509', '0.864', '-0.0321', '-0.4702', '0.1321', '0.1488', '-0.3765', '0.0705', '-0.4973', '-0.3987', '-0.2817', '0.549', '0.9365', '-0.4307', '0.7715', '-0.0819', '-0.868', '0.5205', '-0.1317', '0.4587', '0.00516', '-0.3242', '0.4548', '-0.155', '0.4226', '0.402', '0.00901', '0.1705', '0.229', '-0.002123', '0.2769', '0.3547', '0.2627', '-0.01219', '0.04904', '0.05997', '-0.5063', '-0.5146', '0.11334', '0.8857', '-0.1362', '0.53', '-0.681', '0.11975', '0.165']",,,C562900,,,,
mondo:0007672,glomuvenous malformation,"['familial glomangioma', 'GLOMUVENOUS malformations', 'hereditary glomangioma', 'multiple glomus tumors', 'glomangiomas, multiple', 'multiple glomus tumours', 'glomus tumors, multiple', 'Venous malformations with glomus cells', 'glomangiomatosis', 'GVM', 'hereditary multiple glomangiomas', 'VMGLOM']",7996,138000,83454,C1841984,"['0.5835', '-0.211', '-0.857', '-0.2145', '0.315', '0.01727', '-0.1522', '-0.07965', '-0.4507', '-0.432', '-0.425', '0.2888', '0.0917', '0.2098', '0.02637', '0.5435', '0.11346', '-0.598', '0.3342', '-0.4104', '-0.2201', '0.2817', '1.034', '-0.3347', '0.007633', '0.011536', '0.1697', '0.10254', '0.2795', '0.3933', '0.497', '-0.341', '-0.3054', '0.1359', '-0.11554', '-0.1991', '-0.0609', '-0.5845', '0.7817', '-0.1938', '0.477', '-0.2051', '0.6157', '-0.3235', '0.4907', '-0.3296', '-0.575', '0.1917', '0.5713', '0.2327', '-0.11566', '-0.1245', '-0.52', '0.1447', '-0.4707', '0.1316', '0.4656', '0.2273', '-0.667', '0.3152', '0.10284', '0.3398', '-0.362', '-0.494', '-0.04996', '0.3052', '0.3965', '0.7295', '-0.1279', '0.3574', '-0.2666', '-0.1837', '-0.01045', '-0.04486', '0.1357', '0.3052', '0.3984', '-0.1814', '0.2747', '-0.7974', '-0.6533', '-0.4197', '0.1766', '0.1422', '-0.277', '-0.5366', '0.121', '0.5044', '-0.2332', '-0.002201', '-0.06604', '-0.1602', '-0.0948', '0.545', '0.9663', '-0.278', '0.7075', '-0.9517', '0.18', '-0.2693']",C5350,,C536827,,,10018381,
mondo:0007673,Glucoglycinuria,['Glucoglycinuria'],,138070,,C0268536,,,,C562670,,,,
mondo:0007674,glucose-6-phosphate dehydrogenase-like,"['glucose-6-phosphate dehydrogenase-like', 'G6PDL']",,138110,,,,,,,,,,
mondo:0007675,"glutamic acid decarboxylase, brain, membrane form","['glutamic acid decarboxylase, brain, membrane form']",,138277,,,,,,,,,,
mondo:0007676,glutathione transferase activity toward trans-stilbene oxide,"['trans-stilbene oxide glutathione transferase activity', 'glutathione transferase activity toward trans-stilbene oxide']",,138340,,,,,,,,,,
mondo:0007677,hyperglycinuria,"['glycinuria with or without oxalate urolithiasis', 'hyperglycinuria', 'glycinuria with or without oxalate nephrolithiasis', 'hyperglycinuria (disease)', 'Iminoglycinuria type 2']",,138500,,C0543541,,,,C563009,,,,0003108
mondo:0007679,GMS syndrome,"['Goniodysgenesis-intellectual disability-short stature syndrome', 'Goniodysgenesis--mental retardation--short stature syndrome', 'Goniodysgenesis--intellectual disability--short stature syndrome', 'GMS syndrome']",,138770,2090,C1841854,,,,C564214,,,,
mondo:0007680,multinodular goiter-cystic kidney-polydactyly syndrome,"['MNG/CRD/Da', 'multinodular goiter, cystic renal disease, and digital anomalies', 'multinodular goitre - cystic kidney - polydactyly', 'goiter, multinodular, cystic renal disease, and digital anomalies', 'Daneman-Davy-Mancer syndrome', 'thyroid-renal-digital anomalies', 'multinodular goiter/cystic renal disease/digital anomalies', 'multinodular goiter - cystic kidney - polydactyly', 'Daneman Davy Mancer syndrome']",,138790,2091,C1841853,,,,C535986,,,,
mondo:0007681,"goiter, multinodular 1, with or without Sertoli-Leydig cell tumors","['goiter, nontoxic, with Intrathyroidal calcification', 'multinodular goiter, adolescent', 'familial MNG', 'FMNG', 'goiter, multinodular 1, with or without Sertoli-Leydig cell tumors', 'simple goiter', 'euthyroid goiter', 'simple goitre', 'MNG1', 'euthyroid goitre']",,138800,276399,CN202615,"['-0.603', '0.2218', '-0.444', '0.4033', '0.1103', '0.257', '0.1882', '0.2832', '-0.543', '-0.1244', '0.623', '-0.02469', '-0.4229', '0.2537', '-0.4973', '0.4136', '-0.613', '-0.1764', '-0.4426', '-0.2395', '-0.00381', '-0.547', '0.1857', '-0.462', '-0.1173', '-0.1019', '-0.0834', '-0.1483', '0.3015', '-0.29', '0.8345', '0.2074', '0.0855', '0.1054', '-0.1809', '0.05408', '-0.0552', '0.3628', '0.9023', '0.003462', '-0.2234', '0.5713', '0.2524', '-0.2069', '0.723', '-0.02493', '0.594', '0.012314', '0.3462', '0.3674', '-0.1573', '-0.01508', '0.01176', '0.2966', '-0.644', '0.404', '0.2174', '0.1241', '-0.4172', '-0.4521', '0.634', '0.5557', '-0.2292', '-0.4583', '-0.674', '1.037', '0.4841', '0.4426', '-0.358', '0.7583', '0.02573', '0.5156', '0.2583', '-0.372', '0.09186', '0.565', '-0.04666', '0.4526', '-0.2566', '-0.2542', '-0.2495', '0.10724', '-0.2537', '-0.5386', '0.532', '-0.1825', '0.0892', '0.1733', '0.9097', '0.5347', '-0.246', '-0.09607', '-0.4456', '-0.06586', '0.5947', '-0.1628', '-0.4524', '-0.1315', '-0.391', '0.1788']",,,C562732,240.0,,,
mondo:0007682,granddad syndrome,"['Growth retardation, aged facies, normal development, decreased subcutaneous fat, autosomal dominant inheritance', 'granddad syndrome']",,138920,,C1841836,,,,C564211,,,,
mondo:0007683,Grant syndrome,"['Grant syndrome', 'persistent wormian bones, blue sclerae, mandibular hypoplasia, shallow glenoid fossae and campomelia']",,138930,2097,C1841835,,,,C537293,,,,
mondo:0007685,granulosis rubra nasi,['granulosis rubra nasi'],,139000,,C0263471,,,,C562483,705.89,,,
mondo:0007686,gray platelet syndrome,"['bleeding disorder, Platelet-type, 4', 'GPS', 'platelet-type bleeding disorder 4', 'Alpha storage pool deficiency', 'gray platelet syndrome', 'platelet alpha-granule deficiency', 'marked decrease or absence of alpha-granules and of platelet-specific alpha-granule proteins', 'BDPLT4']",0111044,139090,721,CN205641,"['-0.2468', '-0.289', '-0.488', '-0.07336', '0.11584', '-0.1024', '-0.3452', '1.104', '-0.1641', '0.0764', '0.06964', '0.2827', '0.2054', '0.4539', '0.4275', '0.06976', '-0.1779', '0.2034', '0.3235', '-0.798', '-0.05963', '-0.4973', '0.772', '-0.38', '0.1454', '-0.4866', '-0.252', '0.11005', '0.1271', '-0.08813', '0.3772', '-0.2996', '0.4766', '0.4377', '-0.04276', '-0.3206', '-0.4907', '-0.5933', '0.6006', '-0.2683', '0.421', '-0.08057', '0.064', '-0.587', '0.414', '-0.5386', '-0.294', '0.0924', '0.2285', '-0.002325', '0.331', '0.21', '0.2778', '0.2585', '0.1139', '0.5537', '0.472', '-0.196', '-0.0869', '-0.03134', '-0.324', '-0.02592', '0.4832', '-0.721', '0.05966', '0.06903', '-0.09607', '0.4836', '-0.1821', '0.4702', '-0.4421', '-0.3594', '-0.4077', '0.1538', '0.427', '-0.0933', '0.69', '-0.02713', '0.386', '-0.2118', '-0.253', '-0.5312', '0.2188', '0.0896', '-0.4226', '0.3906', '0.154', '0.02397', '0.3137', '-0.527', '0.498', '0.4592', '-0.332', '-0.2534', '0.5044', '0.5864', '0.1548', '-0.4187', '0.4211', '-0.1897']",C84741,,D055652,,,,
mondo:0007687,"graying of hair, precocious","['White hair, premature', 'graying of hair, precocious']",,139100,,C1841809,,,,C564209,,,,
mondo:0007688,Myhre syndrome,"['LAPS syndrome', 'MYHRE syndrome', 'facial dysmorphism - intellectual deficit - short stature - hearing loss', 'Growth-mental deficiency syndrome of Myhre', 'laryngotracheal stenosis, arthropathy, prognathism, and short stature', 'Growth mental deficiency syndrome of Myhre', 'Myhre syndrome', 'facial dysmorphism-intellectual disability-short stature-hearing loss syndrome', 'MYHRS']",,139210,2588,C0796081,"['0.3037', '-0.3176', '0.0686', '-0.1569', '0.2842', '-0.0782', '1.018', '0.8994', '-0.558', '-0.678', '-0.3608', '0.1542', '-0.604', '0.1766', '-0.345', '-0.135', '0.1764', '-0.3281', '-0.6177', '-0.7266', '0.526', '-0.3254', '0.205', '0.1423', '-0.008514', '-0.3953', '-0.1808', '0.454', '0.452', '0.203', '0.779', '-0.2454', '0.4297', '-0.01906', '0.1722', '-0.2786', '-0.2224', '-0.2297', '-0.11224', '0.41', '0.4924', '-0.2783', '0.2306', '0.3406', '0.521', '0.1478', '0.1973', '0.4053', '-0.335', '0.1334', '-0.578', '-0.0846', '0.5254', '0.01338', '-0.3132', '-0.2808', '-0.3135', '0.0896', '0.1339', '-0.1011', '-0.10767', '0.7803', '-0.5723', '0.001484', '0.3523', '-0.719', '-0.02533', '0.4175', '-0.1836', '0.1195', '0.03087', '-0.2544', '-0.4336', '-0.1841', '-0.05768', '-0.2072', '0.711', '-0.5796', '-0.494', '-0.1775', '0.489', '-0.1832', '-0.517', '0.6445', '-0.3267', '0.343', '-0.08484', '0.901', '0.429', '0.1389', '0.11304', '0.1361', '-0.155', '0.617', '0.4468', '-0.0738', '0.2487', '-0.4028', '0.1299', '0.329']",C123815,,C537620,759.89,,,
mondo:0007689,guanylate kinase 3,"['guanylate kinase 3', 'GUK3', 'guanylate kinase type 3', 'guanylate KINASE 3']",,139290,,,,,,,,,,
mondo:0007690,aromatase excess syndrome,"['AEXS', 'gynecomastia, familial, due to increased aromatase activity', 'gynecomastia, hereditary', 'increased aromatase activity', 'aromatase excess syndrome', 'aromatase activity, increased', 'hereditary prepubertal gynecomastia', 'familial hyperestrogenism']",0090122,139300,178345,C1970109,"['-0.5176', '0.000597', '-0.1039', '-0.3252', '0.4229', '-0.0984', '-0.1985', '1.097', '-0.668', '-0.1349', '0.00469', '0.729', '0.04095', '0.5356', '0.3901', '-0.2024', '0.4167', '0.1195', '-0.8433', '-0.7104', '-0.187', '-0.2477', '0.724', '-0.4666', '0.3755', '0.1969', '0.2115', '-0.3333', '-0.04782', '-0.09424', '1.026', '-0.486', '0.943', '0.3408', '-0.0455', '-0.06915', '-0.266', '-0.125', '-0.0708', '0.07965', '0.4922', '0.3787', '-0.0386', '0.04083', '-0.1099', '-0.4421', '0.4133', '0.1009', '-0.013084', '0.1792', '0.4097', '-0.2522', '-0.1293', '0.02007', '-0.1572', '0.1377', '0.4941', '-0.661', '-0.0391', '0.002409', '0.374', '0.4001', '0.0782', '-0.2583', '0.3337', '0.2803', '0.2372', '0.517', '-0.2888', '-0.4595', '0.06445', '0.3374', '0.196', '-0.2137', '0.4458', '-0.702', '0.0389', '0.3535', '-0.2416', '-0.2058', '-0.1233', '0.533', '0.126', '-0.237', '0.3', '-0.03387', '0.3083', '-0.2654', '0.5786', '-0.01907', '0.1891', '0.67', '-0.2131', '-0.06174', '0.5825', '0.3516', '0.235', '-0.1667', '0.1736', '-0.0956']",,,C000591739,259.8,,,
mondo:0007691,"Guillain-Barre syndrome, familial","['neuropathy, inflammatory demyelinating', 'GBS', 'polyneuropathy, inflammatory demyelinating, acute', 'AIDP', 'Guillain-Barre syndrome, familial']",,139393,2932,,,,,,,,10057645,
mondo:0007693,hypertrichosis cubiti-short stature syndrome,"['MacDermot-Patton-Williams syndrome', 'hairy elbows', 'hypertrichosis cubiti', 'hairy elbows syndrome']",,139600,2220,C1841696,,,,C535618,,,10068636,
mondo:0007694,hairy nose tip,"['hairy nose tip', 'HNT']",,139630,,,,,,C535619,,,,
mondo:0007695,hairy palms and soles,"['circumscribed hairy Dysembryoplasia of palms', 'hairy palms and soles', 'hairy cutaneous malformations of palms and soles', 'thickened hair-bearing skin on the palms of both hands']",,139650,,,,,,C535620,,,,
mondo:0007696,Emery-Nelson syndrome,"['familial syndrome of short stature, deformities of the hands and feet, and unusual facies', 'hand and foot deformity with flat facies', 'hand and foot deformity - flat facies', 'hand and foot deformity-flat facies syndrome']",,139750,1927,C1841693,,,,C535626,,,,
mondo:0007697,hand clasping pattern,['hand clasping pattern'],,139800,,,,,,,,,,
mondo:0007698,hand-foot-genital syndrome,"['HFG', 'hand foot uterus syndrome', 'hand-foot-genital syndrome', 'HFU syndrome', 'HFGS', 'hand-foot-uterus syndrome', 'hand foot genital syndrome', 'HFG syndrome']",0060739,140000,2438,C1841679,"['-0.2323', '0.02383', '0.1709', '-0.2397', '0.1729', '-0.1874', '-0.07776', '0.2257', '-0.211', '-0.1853', '0.001629', '-0.01054', '-0.01976', '0.014084', '-0.1831', '-0.0754', '-0.04388', '-0.04626', '-0.0826', '-0.3032', '0.04343', '0.06934', '0.2296', '0.00446', '0.1283', '0.07336', '-0.1053', '-0.06696', '0.2693', '-0.2238', '0.1603', '0.04877', '0.1575', '0.2263', '0.1603', '-0.1023', '-0.005844', '-0.06177', '-0.11115', '-0.1813', '0.10846', '-0.2527', '0.06305', '-0.138', '0.03021', '-0.2778', '-0.09247', '0.2927', '0.1053', '-0.02058', '-0.1501', '-0.04074', '-0.00497', '-0.0773', '-0.3413', '-0.1486', '0.0721', '-0.1179', '-0.245', '-0.0002868', '0.1857', '0.002104', '-0.02173', '0.1232', '-0.04807', '0.01785', '0.2438', '0.08984', '-0.2522', '0.1122', '-0.264', '0.01128', '0.06573', '0.01277', '0.05313', '-0.01982', '0.05295', '-0.06415', '-0.2004', '-0.2097', '-0.0588', '0.0447', '0.0717', '0.2756', '-0.05643', '-0.07086', '0.00974', '0.2107', '0.01222', '-0.0992', '0.119', '0.2598', '0.1743', '0.0914', '0.4612', '-0.0669', '0.4177', '-0.351', '0.002836', '0.2058']",,,C535627,759.89,,10072361,
mondo:0007699,Hashimoto thyroiditis,"['Hashimoto struma', 'chronic lymphocytic thyroiditides', 'lymphocytic thyroiditis', 'Hashimoto^s thyroiditis', 'Ht', 'Hashimoto disease', 'thyroiditides, chronic lymphocytic', 'Hashimotos syndrome', 'chronic lymphocytic thyroiditis', 'thyroid autoantibodies', 'disease, Hashimoto^s', 'lymphocytic thyroiditides, chronic', 'lymphocytic thyroiditis, chronic', 'Hashimoto^s syndrome', 'Hashimoto hypothyroidism', 'hypothyroidism, autoimmune thyroid autoantibodies, included', 'thyroiditis, chronic lymphocytic', 'Hashimoto^s syndromes', 'disease, Hashimoto', 'thyroiditides, Hashimoto', 'Hashimotos disease', 'syndromes, Hashimoto^s', 'HT', 'thyroiditis, Hashimoto', 'syndrome, Hashimoto^s', 'Hashimoto thyroiditis', 'Hashimoto^s struma', 'Hashimoto thyroiditides', 'Hashimoto syndrome', 'autoimmune thyroiditis', 'hypothyroidism, autoimmune', 'Hashimoto^s disease']",7188,140300,855,C0677607,"['-0.3464', '0.2888', '-0.0974', '0.0269', '0.1558', '-0.1709', '0.09515', '-0.276', '-0.07184', '-0.1826', '0.02959', '0.0867', '-0.003077', '0.01857', '0.0659', '-0.1068', '-0.2104', '0.0517', '-0.2028', '-0.5103', '0.1954', '-0.205', '0.299', '-0.3425', '0.2761', '0.1882', '0.04556', '0.04016', '0.02672', '-0.3154', '0.258', '0.2036', '0.2407', '0.1059', '0.041', '-0.0857', '-0.2478', '0.07983', '-0.03928', '-0.0752', '-0.0892', '0.2842', '0.2415', '-0.04456', '-0.0947', '-0.3875', '0.5317', '-0.1493', '0.3855', '0.01064', '0.01069', '0.2432', '0.3716', '0.0963', '-0.36', '0.0676', '0.2198', '-0.512', '-0.523', '0.1022', '0.1835', '0.2837', '-0.01746', '-0.06445', '0.1168', '0.2167', '0.3596', '0.3914', '-0.551', '0.2507', '-0.1655', '-0.0783', '-0.10876', '-0.2646', '0.3345', '0.10205', '0.11304', '0.2108', '-0.038', '-0.1654', '-0.3118', '-0.2659', '-0.2318', '-0.2333', '-0.2212', '-0.2515', '0.2404', '0.1003', '0.279', '-0.2091', '0.2367', '0.159', '0.01013', '-0.2693', '0.5244', '0.1931', '0.0782', '-0.1329', '-0.1633', '0.266']",C27191,0003779,D050031,245.2,E06.3,,
mondo:0007700,hawkinsinuria,"['hawkinsinuria', '4-alpha-hydroxyphenylpyruvate hydroxylase deficiency', '4-HPPD deficiency', '4-hydroxyphenylpyruvic acid dioxygenase deficiency']",0111362,140350,2118,C2931042,"['-0.2954', '0.3313', '-0.0686', '0.316', '0.2173', '-0.3667', '-0.822', '0.2418', '-0.1501', '-0.01659', '-0.003252', '-0.2152', '0.0527', '-0.1577', '-0.2605', '0.3838', '0.3286', '-0.03955', '-0.2443', '-0.9575', '-0.371', '-0.3047', '0.2786', '-0.2952', '0.1171', '-0.2106', '-0.4043', '0.08246', '-0.0268', '-0.2834', '0.4365', '-0.003832', '0.3096', '0.0001162', '-0.1517', '0.1459', '-0.07837', '0.1716', '-0.1813', '0.2747', '0.2783', '-0.4202', '0.0678', '-0.1357', '-0.5107', '-0.21', '0.0817', '0.04318', '0.1179', '0.1481', '-0.5425', '-0.219', '0.06934', '0.0902', '-0.59', '-0.0958', '0.1898', '-0.1842', '-0.6333', '0.1373', '0.5947', '0.346', '0.01614', '-0.2432', '0.343', '0.2144', '0.621', '-0.2175', '-0.1256', '0.3022', '0.06586', '0.09216', '-0.2273', '0.4097', '0.1404', '0.67', '0.011475', '-0.728', '-0.3296', '0.05777', '-0.05356', '-0.1576', '0.1589', '-0.097', '0.3442', '0.2922', '0.01663', '-0.0842', '0.4958', '0.4756', '0.3293', '0.2515', '-0.3816', '0.0646', '0.0666', '0.77', '0.07043', '-0.066', '0.1438', '0.3333']",,,C535845,,,,
mondo:0007701,progressive familial heart block type II,"['progressive familial heart block, type II', 'progressive familial heart block type 2', 'heart block progressive familial type 2', 'PFHBII', 'PFHB2']",0111075,140400,,,,,,C564202,426.6,,,
mondo:0007702,heart-hand syndrome type 3,"['Cardiomelic syndrome type 3', 'upper limb malformations and congenital cardiac anomalies', 'heart-hand syndrome, Spanish type', 'atriodigital dysplasia type 3', 'brachydactyly and intraventricular conduction defect', 'heart-limb syndrome type 3']",,140450,1342,C1841657,"['0.153', '0.2035', '0.007744', '0.3684', '0.1652', '-0.46', '0.1357', '0.627', '-0.2032', '-0.4634', '-0.4092', '-0.1578', '-0.3958', '0.0157', '-0.507', '-0.0096', '-0.2769', '0.1747', '0.1813', '-0.2172', '0.0976', '0.484', '0.718', '-0.05142', '0.06476', '0.408', '-0.288', '0.4062', '0.5103', '-0.2239', '0.1674', '-0.2496', '-0.1534', '-0.2026', '0.5503', '-0.4346', '-0.1713', '-0.3447', '-0.3828', '-0.6875', '-0.114', '-0.2947', '0.004494', '0.1667', '0.03067', '-0.2546', '-0.12085', '1.135', '-0.3293', '-0.2573', '-0.1285', '-0.4604', '-0.0562', '-0.462', '-0.951', '-1.108', '0.1698', '-0.3293', '-0.412', '0.1523', '0.0896', '-0.3455', '0.2139', '0.25', '-0.378', '-0.2827', '0.4058', '0.1016', '-0.517', '-0.2856', '-0.3145', '-0.1248', '0.3022', '0.3987', '0.1853', '0.4363', '-0.819', '0.2123', '-0.5283', '-0.4773', '-0.02266', '-0.4353', '0.5625', '0.207', '0.394', '-0.323', '0.3765', '0.68', '0.7974', '0.1647', '-0.1156', '0.269', '0.3552', '0.37', '0.3103', '0.1787', '0.3179', '-1.122', '-0.4463', '0.2335']",,,C535853,,,,
mondo:0007704,osteoarthritis susceptibility 2,"['Dipoa', 'hand osteoarthritis', 'osteoarthritis of distal interphalangeal joints', 'Heberden nodes', 'osteoarthritis caused by mutation in MATN3', 'OS2', 'osteoarthritis susceptibility type 2', 'osteoarthritis susceptibility 2', 'MATN3 osteoarthritis', 'OADIP']",,140600,,,,,,,,,,
mondo:0007705,Heinz body anemia,"['Heinz body anemias', 'Heinz body anemias, alpha-']",0111363,140700,178330,C0700299,"['-0.1816', '0.3555', '-0.2383', '0.3044', '0.8467', '-0.1246', '-0.252', '0.3545', '-0.1718', '-0.278', '0.7544', '-0.03314', '0.1073', '0.3103', '-1.363', '-0.1855', '-0.646', '0.3643', '-0.3962', '-0.507', '-0.1498', '-0.4822', '0.3752', '-0.3523', '0.668', '-0.4028', '-0.01974', '-0.2062', '0.524', '0.3247', '0.1716', '0.0346', '0.3665', '0.6353', '0.4321', '-0.0774', '-0.9575', '-0.3247', '0.476', '-0.566', '-0.753', '0.3386', '0.0868', '-0.2905', '-0.758', '-0.888', '0.171', '0.1926', '0.497', '-0.1497', '0.5522', '0.3633', '0.7915', '-0.1445', '0.5195', '-0.8267', '0.2373', '0.538', '-1.087', '0.2499', '-0.1373', '0.2996', '-0.1115', '-0.4036', '-0.3708', '0.3032', '0.2483', '0.743', '-0.6777', '0.987', '0.966', '-0.2744', '-0.4263', '-0.7217', '0.2211', '0.9375', '0.2532', '0.2144', '-0.01648', '0.342', '0.1489', '-0.1246', '-0.211', '0.1317', '0.411', '-0.5435', '-0.743', '0.4287', '0.9873', '-0.1921', '0.5654', '0.012276', '-0.1588', '-0.05783', '0.5303', '1.111', '0.0726', '-0.1698', '-0.003628', '-0.4634']",,,C563030,,,10002058,0005511
mondo:0007706,cavernous hemangiomas of face-supraumbilical midline raphe syndrome,"['hemangiomas cavernous of face supraumbilical midline raphe', 'supraumbilical midabdominal raphe and facial cavernous hemangiomas', 'raphe, supraumbilical Midline, with cavernous Facial hemangiomas', 'hemangiomas, cavernous, of face and supraumbilical MIDLINE raphe', 'sternal nonunion with supraumbilical raphe']",,140850,2124,C0472694,,,,C538144,,,,
mondo:0007707,hemangiomas of small intestine,"['hemangiomas of small intestine', 'small intestine hemangioma']",,140900,,C1841654,,,,C564201,,,,
mondo:0007708,Kasabach-Merritt syndrome,"['hemangioma thrombocytopenia syndrome', 'hemangiomatosis with thrombocytopenia', 'hemangioma-hemorrhage syndrome', 'Kasabach Merritt syndrome', 'hemangioma-thrombocytopenia syndrome', 'Kasabach Merritt phenomenon', 'Kasabach-Merritt syndrome', 'KMP', 'thrombocytopenia-hemangioma syndrome', 'thrombopenia-hemangioma syndrome']",,141000,2330,C0221025,,C3821,,D059885,287.39,,10058423,
mondo:0007709,"hematuria, benign familial","['thin-basement-membrane nephropathy', 'hematuria, familial benign', 'BFH', 'thin membrane nephropathy', 'hematuria, benign familial']",0111365,141200,97562,,,,,C562476,,,,
mondo:0007710,facial hemiatrophy,"['hemifacial atrophy, progressive', 'progressive hemifacial atrophy', 'PHA', 'hemifacial atrophy', 'Romberg syndrome', 'progressive facial hemiatrophy', 'HFA', 'parry-Romberg syndrome', 'Romberg hemi-facial atrophy']",1757,141300,1214,C0015458,,C116916,,D005150,,,,
mondo:0007711,Bencze syndrome,"['Bencze syndrome', 'hemifacial hyperplasia with strabismus', 'hemifacial hyperplasia-strabismus syndrome', 'hemifacial hyperplasia strabismus']",,141350,1241,C1841640,,,,C564199,,,,
mondo:0007712,oculoauriculovertebral spectrum with radial defects,"['Moeschler-Clarren syndrome', 'oculoauriculovertebral spectrum with radial defect', 'hemifacial microsomia-radial defects syndrome', 'Goldenhar syndrome with ipsilateral radial defect', 'microsomia hemifacial radial defects', 'Oavs with radial defect', 'hemifacial microsomia with radial defects', 'Moeschler Clarren syndrome']",,141400,2549,,,,,,,,,
mondo:0007713,clonic hemifacial spasm,"['hemifacial spasm, familial', 'focal myoclonus of face', 'hemifacial spasm', 'facial hemispasm']",,141405,221083,C3536936,,,,C564198,,G51.3,,
mondo:0007715,hemolytic poikilocytic anemia due to reduced ankyrin binding sites,['hemolytic poikilocytic anemia due to reduced ankyrin binding sites'],,141700,,C1841622,,,,C564197,,,,
mondo:0007716,alpha thalassemia-intellectual disability syndrome type 1,"['alpha-thalassemia-intellectual disability syndrome linked to chromosome 16', 'ATR-16 syndrome', 'Alpha-thalassemia-intellectual disability syndrome linked to chromosome type 16', 'chromosome 16P deletion syndrome', 'mental retardation with Haemoglobin H', 'Alpha-thalassemia/intellectual disability syndrome, deletion-type', 'Haemoglobin H-related mental retardation', 'intellectual disability with Haemoglobin H', 'Haemoglobin H-related intellectual disability', 'Alpha thalassemia-mental retardation syndrome', 'Alpha thalassemia-intellectual disability syndrome, deletion type', 'alpha thalassemia-retardation syndrome', 'ATR syndrome, deletion type', 'ATR syndrome linked to chromosome 16', 'Alpha-thalassemia/mental retardation syndrome, deletion-type', 'Hemoglobin H-related mental retardation', 'ALPHA-thalassemia/intellectual disability syndrome, chromosome 16-related', 'Alpha thalassemia-intellectual disability syndrome', 'mental retardation with Hemoglobin H', 'Hemoglobin H-related intellectual disability', 'alpha-thalassemia/mental retardation syndrome, type 1', 'alpha-thalassemia/mental retardation syndrome, deletion-type', 'ATR, deletion-type', 'alpha-thalassemia/intellectual disability syndrome, deletion-type', 'alpha thalassemia-intellectual disability syndrome, deletion type', 'ALPHA-thalassemia/mental retardation syndrome, chromosome 16-related', 'alpha-thalassemia/intellectual disability syndrome, type 1', 'intellectual disability with Hemoglobin H']",0110029,141750,98791,C0795917,,,,C563050,282.49,D56.0,,
mondo:0007717,hemoglobin--variants for which the chain carrying the mutation 1S unknown or uncertain,['HEMOGLOBIN--variants FOR which the chain carrying the mutation IS unknown or uncertain'],,142309,,C1840647,,,,,,,,
mondo:0007718,"hepatic adenomas, familial","['liver cell adenomas, familial', 'hepatic adenoma, somatic', 'hepatic adenomas, familial']",0111366,142330,,C1840646,,,,C564190,,,,
mondo:0007719,diaphragmatic hernia 1,"['diaphragm, complete agenesis of', 'hernia, congenital diaphragmatic', 'diaphragmatic hernia, congenital 1', 'DIH1', 'diaphragmatic defect, congenital', 'hemidiaphragm, agenesis of', 'diaphragm, unilateral agenesis of', 'hernia, congenital diaphragmatic 1', 'diaphragmatic hernia, congenital']",,142340,,,,,,,,,,
mondo:0007720,"hernia, double inguinal","['hernia, double inguinal']",,142350,,C0860251,,,,C563164,,,,
mondo:0007721,hiatus hernia,"['hiatus hernia', 'hiatus hernia (disease)', 'hernia, hiatus', 'hiatal hernia', 'diaphragmatic - hiatus -hernia']",12642,142400,,,,C98945,,D006551,,,,0002036
mondo:0007722,heterochromia iridis,"['heterochromia iridis', 'heterochromia iridis (disease)']",,142500,,,,,,C538115,,,,0001100
mondo:0007723,"Hirschsprung disease, susceptibility to, 1","['HSCR1', 'Hirschsprung disease, protection against', 'megacolon, aganglionic', 'aganglionic megacolon', 'Hirschsprung disease, susceptibility to, type 1', 'Hirschsprung disease', 'susceptibility to Hirschsprung disease 1', 'RET Hirschsprung disease', 'Hirschsprung disease, susceptibility to, 1']",,142623,,C2931876,,,,,,,,
mondo:0007724,hirsutism-skeletal dysplasia-intellectual disability syndrome,"['Wiedemann-Oldigs-Oppermann syndrome', 'hirsutism, skeletal dysplasia, and mental retardation', 'hirsutism skeletal dysplasia intellectual disability syndrome', 'Wiedemann Oldigs Oppermann syndrome', 'hirsutism skeletal dysplasia mental retardation syndrome', 'hirsutism, skeletal dysplasia, and intellectual disability']",,142625,2156,C0795976,,,,C536705,,,,
mondo:0007725,hereditary progressive mucinous histiocytosis,"['histiocytosis, progressive mucinous']",,142630,158025,C1840586,,,,C564186,,,,
mondo:0007726,"hip dysplasia, Beukes type","['Beukes hip dysplasia', 'Cilliers-Beighton syndrome', 'BFHD', 'hip dysplasia Beukes type', 'osteoarthropathy, premature degenerative, of hip', 'BHD', 'Beukes familial hip dysplasia', 'hip dysplasia, Beukes type', 'premature degenerative osteoarthropathy of the hip']",0111367,142669,2114,,"['-0.3203', '-0.1844', '-0.3184', '0.0242', '-0.1305', '-0.9917', '-0.4458', '1.268', '-0.733', '-0.7026', '-0.004166', '-0.0857', '-0.049', '0.863', '0.2062', '-0.4302', '-0.2725', '-0.2358', '0.2957', '-1.348', '-0.1763', '0.316', '1.066', '0.341', '0.2161', '0.6587', '0.4338', '-0.1121', '0.02753', '-0.0827', '-0.1812', '-0.535', '0.281', '0.8125', '0.4053', '0.3455', '-0.1514', '-0.2253', '-0.004856', '-0.2094', '0.8013', '-0.1927', '-0.8745', '-0.1986', '-0.1477', '-0.2134', '-0.1128', '-0.0318', '0.3804', '0.06964', '0.5024', '0.3428', '0.5156', '0.2742', '-0.326', '-0.576', '-0.997', '0.06027', '-0.3442', '-0.6797', '0.849', '0.5596', '-0.695', '0.4', '-0.5117', '-0.1121', '0.769', '0.3267', '0.2192', '-0.2944', '0.696', '0.1378', '0.02419', '-0.3088', '-0.1974', '0.0464', '-0.2546', '1.235', '0.1914', '-0.3574', '-0.5977', '0.03207', '-0.2776', '0.5435', '0.1407', '0.1879', '0.2251', '0.01187', '0.963', '0.3086', '-0.2874', '-0.1203', '-0.2207', '0.34', '-0.05548', '-0.514', '0.9097', '-0.01446', '-0.03885', '0.255']",,,C564185,,,,
mondo:0007727,autosomal dominant familial periodic fever,"['tumor necrosis factor receptor 1 associated periodic syndrome', 'familial Hibernian fever', 'periodic FEVER, familial, autosomal dominant', 'TNF receptor 1-associated periodic syndrome', 'TRAPS syndrome', 'TRAPS', 'TNF receptor-associated periodic syndrome', 'tumor necrosis factor receptor-associated periodic syndrome', 'FPF', 'tumour necrosis factor receptor 1-associated periodic syndrome', 'FHF', 'Hibernian fever, familial', 'tumour necrosis factor receptor-associated periodic syndrome', 'tumor necrosis factor receptor 1-associated periodic syndrome', 'tumour necrosis factor receptor 1 associated periodic syndrome', 'TNF receptor-associated periodic fever syndrome']",0090018,142680,32960,,"['0.3948', '0.472', '-0.5347', '0.476', '0.0399', '-0.1403', '-0.0635', '0.2164', '-0.627', '-0.1737', '0.2634', '0.3535', '0.2054', '0.2922', '-0.7617', '0.177', '-0.1608', '-0.1744', '0.1893', '-0.1697', '0.1367', '-0.37', '0.1025', '-0.01764', '-0.288', '-0.2275', '-0.2568', '0.396', '-0.4375', '0.155', '-0.0682', '0.05728', '0.0935', '-0.1964', '-0.312', '0.483', '-0.7617', '0.02043', '-0.02328', '-0.689', '0.2659', '-0.416', '-0.10876', '-0.4148', '0.4568', '0.5996', '-0.4973', '-0.2477', '-0.471', '0.8965', '-0.8057', '0.0488', '0.185', '0.3643', '-0.162', '0.3298', '-0.3093', '0.0716', '-0.1564', '-0.12366', '0.1389', '-0.02873', '-0.01515', '-0.0823', '0.59', '-0.12103', '0.4692', '0.4163', '0.05267', '0.4348', '-0.3926', '0.634', '-0.1638', '-0.8135', '0.405', '0.6855', '-0.085', '0.314', '0.5215', '-0.4575', '0.0958', '-0.03134', '0.1654', '0.1893', '0.0912', '-0.1628', '0.264', '0.9277', '0.4812', '0.1151', '0.315', '-0.1477', '0.2866', '-0.051', '0.4763', '0.351', '0.1838', '-0.5713', '-0.2283', '-0.4038']",C119051,,C536657,,,,
mondo:0007728,"acne inversa, familial, 1","['NCSTN familial acne inversa', 'acne inversa, familial, 1', 'acne inversa, familial, type 1', 'familial acne inversa caused by mutation in NCSTN', 'ACNINV1', 'hidradenitis suppurativa, familial', 'acne inversa, familial']",,142690,,CN028850,"['-0.01723', '0.05588', '-0.01273', '-0.03065', '0.001974', '-0.05624', '0.00801', '0.06476', '-0.0516', '-0.00975', '-0.01089', '-0.0173', '-0.015335', '0.01892', '-0.0566', '-0.04498', '0.012215', '-0.01752', '0.01199', '-0.10516', '-0.02646', '-0.01723', '0.0571', '-0.0185', '0.02162', '-0.01505', '0.00653', '-0.00969', '0.004917', '-0.05032', '0.05783', '-0.015335', '0.07214', '0.03105', '0.001851', '-0.02379', '-0.02803', '-0.01881', '0.00383', '-0.053', '0.03778', '-0.0671', '0.02646', '-0.03017', '-0.001825', '-0.0487', '-0.0256', '0.0413', '-0.002975', '0.01148', '-0.011246', '-0.0314', '0.03014', '0.003748', '-0.03583', '-0.01607', '0.05765', '-0.04214', '-0.0819', '-0.00907', '0.02783', '0.01909', '0.01591', '0.00617', '0.00794', '0.023', '0.06186', '0.0262', '-0.05508', '0.0701', '-0.03775', '0.007366', '-0.0005045', '-0.0372', '0.0326', '0.0377', '0.00849', '0.001371', '-0.04126', '-0.03366', '-0.00749', '0.02779', '-0.02489', '0.01978', '-0.00549', '0.00764', '0.03152', '0.06143', '0.07495', '-0.00239', '0.01113', '0.03967', '0.01656', '0.01073', '0.10956', '0.03088', '0.06085', '-0.0872', '-0.01273', '0.004665']",,,,,,,
mondo:0007729,developmental dysplasia of the hip 1,"['hip dysplasia, congenital', 'DDH1', 'acetabular dysplasia', 'hip dysplasia, developmental', 'developmental dysplasia of the hip 1']",,142700,,,,,,,,,,
mondo:0007730,histiocytic dermatoarthritis,['histiocytic dermatoarthritis'],,142730,,C1840551,,,,C564183,,,,
mondo:0007732,Holt-Oram syndrome,"['heart-hand syndrome, type 1', 'heart-hand syndrome type 1', 'Cardiac-limb syndrome', 'HOLT-Oram syndrome', 'Holt-Oram syndrome', 'atrio-digital syndrome', 'HOS', 'atriodigital dysplasia', 'heart-hand syndrome', 'atriodigital dysplasia type 1', 'HOS 1', 'ventriculo-radial syndrome', 'Hos1', 'atrio digital syndrome']",0060468,142900,392,C0265264,"['0.149', '-0.3958', '0.614', '-0.3567', '0.0494', '0.1555', '0.4397', '0.68', '-0.4976', '-0.6216', '-0.4375', '-0.2773', '0.1919', '0.838', '-0.264', '0.3164', '-0.532', '-0.5146', '-0.6816', '-0.301', '-0.09595', '0.8745', '0.6963', '-0.1054', '0.29', '-0.2147', '0.11', '0.1431', '1.048', '0.10986', '0.1937', '0.1726', '-0.2311', '0.2241', '0.1247', '-0.4673', '0.04962', '-0.6074', '-0.1594', '-0.336', '0.2086', '-0.382', '-0.003384', '0.05127', '0.4465', '-0.3652', '-0.3774', '0.4697', '-0.0656', '0.08057', '-0.3193', '0.0722', '-0.4067', '-0.11804', '-0.684', '-0.2886', '-0.02037', '-0.1178', '-0.06586', '-0.04086', '0.1276', '0.1081', '-0.2377', '0.2603', '-0.414', '-0.0916', '0.4067', '0.3494', '-0.355', '0.04333', '0.1973', '0.1211', '-0.2448', '-0.144', '0.1683', '0.2115', '-0.2219', '-0.403', '-0.8613', '-0.7344', '0.1278', '0.0639', '0.7197', '0.3276', '-0.08484', '-0.2494', '0.3267', '0.1995', '-0.3264', '-0.2537', '0.1705', '-0.0845', '0.0833', '0.00276', '1.022', '-0.00964', '0.95', '-0.2588', '-0.1777', '0.1602']",C125592,,C535326,759.89,,10050469,
mondo:0007733,holoprosencephaly 3,"['HLP3', 'holoprosencephaly type 3', 'HPE3', 'Shh holoprosencephaly', 'holoprosencephaly caused by mutation in Shh', 'SHH holoprosencephaly', 'Hlp3', 'holoprosencephaly 3']",0110875,142945,,C1840529,"['0.00557', '0.06396', '0.02527', '-0.00725', '0.03772', '-0.05954', '0.00634', '0.0813', '-0.07153', '-0.0339', '-0.05603', '-0.01968', '0.03345', '0.0073', '-0.03827', '-0.06055', '-0.002176', '-0.04984', '-0.010666', '-0.0971', '-0.03296', '-0.0072', '0.079', '-0.02696', '0.0483', '-0.013954', '-0.0264', '0.01355', '-0.0102', '-0.03848', '0.07336', '-0.0137', '0.0634', '0.0416', '0.02388', '-0.042', '-0.01259', '-0.0339', '0.004574', '-0.0485', '0.0426', '-0.0701', '0.02197', '-0.0232', '-0.01507', '-0.04755', '-0.02304', '0.0488', '-0.012726', '0.03488', '-0.010445', '-0.01958', '0.01174', '-0.003963', '-0.04224', '-0.01964', '0.05817', '-0.06174', '-0.08624', '0.01671', '0.0481', '0.04587', '0.02757', '0.02678', '-0.01489', '0.003004', '0.0939', '0.0238', '-0.0503', '0.04764', '-0.02948', '0.02757', '0.03473', '-0.078', '0.02821', '0.0341', '0.006615', '-0.02042', '-0.07776', '-0.06445', '-0.01335', '0.005024', '-0.003666', '0.05545', '-0.02614', '-0.02628', '0.03903', '0.1056', '0.0832', '0.00074', '0.01605', '0.0845', '0.01721', '-0.006363', '0.1411', '0.02248', '0.0603', '-0.0837', '-0.0169', '0.01814']",,,C564181,,,,
mondo:0007734,holoprosencephaly 4,"['holoprosencephaly 4', 'TGIF1 holoprosencephaly', 'holoprosencephaly caused by mutation in TGIF1', 'HPE4', 'holoprosencephaly type 4']",0110880,142946,,C1840528,,C75475,,C564180,,,,
mondo:0007735,congenital Horner syndrome,"['congenital Claude-Bernard-Horner syndrome', 'congenital Horner syndrome', 'congenital Horner syndrome (disease)', 'HORNER syndrome, congenital']",,143000,91413,C1840475,,,,C564178,,,,0006837
mondo:0007736,"HPA 1 Recognition polymorphism, beta-globin-related","['HPA I RECOGNITION polymorphism, BETA-globin-RELATED', 'HPA1', 'restriction fragment length polymorphism, sickle cell Anemia-related', 'HPA I RECOGNITION polymorphism, BETA-globin-related']",,143020,,,,,,,,,,
mondo:0007737,humeroradial synostosis,"['humero-radial fusion', 'humeroradial synostosis (disease)', 'humero-radial synostosis', 'humeroradial synostosis']",0060467,143050,3265,,,,,,755.59,,,0003041
mondo:0007738,spondyloepiphyseal dysplasia with congenital joint dislocations,"['spondyloepiphyseal dysplasia', 'CHST3-related skeletal dysplasia', 'Humerospinal dysostosis', 'Gollop Coates syndrome', 'bifurcation of distal humerus with oligoectro-syndactyly', 'SDCD, CHST3 type', 'humero-spinal dysostosis with congenital heart disease', 'SEDCJD', 'spondyloepiphyseal dysplasia with congenital joint dyslocations, CHST3 type', 'spondyloepiphyseal dysplasia with congenital JOINT dislocations', 'chondrodysplasia with multiple dislocations', 'Kozlowski Celermajer tink syndrome', 'Omani type', 'spondyloepiphyseal dysplasia, Omani type', 'spondyloepiphyseal dysplasia with congenital joint dislocations', 'chondrodysplasia with congenital joint dislocations, CHST3 type']",0050813,143095,263463,,"['0.2233', '-0.3503', '-0.3628', '0.58', '-0.2512', '-0.7183', '-0.01636', '0.7246', '-0.6855', '-0.803', '0.3765', '0.216', '0.07666', '0.772', '-0.3638', '-0.3643', '-0.2164', '-0.794', '-0.6978', '0.0175', '0.817', '0.4602', '0.2426', '0.2163', '-0.5073', '0.4043', '-0.537', '0.0759', '-0.0875', '-0.609', '0.1097', '-0.4468', '-0.12396', '0.2341', '0.4666', '-0.2712', '0.0759', '-0.719', '0.577', '-0.8125', '0.10565', '-0.2329', '-0.2329', '0.8613', '-0.0944', '-0.2177', '-0.487', '0.3535', '0.2808', '-0.2585', '-0.1108', '-0.461', '0.899', '0.2534', '0.233', '-0.7783', '-0.4575', '-0.346', '0.04767', '-0.2573', '-0.1566', '0.2192', '-0.891', '0.171', '-0.683', '0.2296', '-0.05063', '0.946', '-0.4053', '0.09204', '-0.02203', '-0.291', '0.08685', '-0.9556', '0.3538', '0.3323', '-0.0977', '0.7617', '0.0258', '-0.441', '-0.4404', '0.3027', '-0.6636', '0.95', '-0.2861', '0.1624', '0.3533', '0.513', '0.539', '0.2198', '0.1699', '0.6733', '-0.3914', '0.4048', '0.03146', '0.2979', '0.404', '-0.2186', '0.6216', '-0.3962']",,,C537283,756.9,,,
mondo:0007739,Huntington disease,"['HD', 'Huntington disease', 'Huntington chorea', 'Huntington^s disease', 'Huntington^s chorea']",12858,143100,399,C0020179,"['0.3228', '0.74', '-0.03111', '0.1395', '-0.3345', '-0.218', '0.4697', '0.6646', '-0.5454', '-0.308', '0.3662', '0.03152', '0.2352', '0.439', '0.821', '-0.572', '-0.771', '0.11035', '-0.2378', '-0.9023', '-0.3389', '-0.372', '0.0135', '-0.545', '-0.03583', '-0.2861', '0.3582', '0.108', '0.2177', '0.1599', '0.434', '-0.556', '0.342', '0.06866', '-0.1857', '-0.3179', '-0.3503', '0.1969', '-0.2986', '-0.2466', '0.9624', '0.1278', '0.1025', '-0.0111', '0.1461', '-0.6104', '-0.52', '-0.708', '-0.01446', '1.194', '0.3062', '0.08997', '-0.5015', '-0.0988', '0.3608', '-0.1302', '0.2133', '0.3906', '0.1155', '-0.2502', '0.13', '0.3083', '0.1237', '0.31', '-0.08167', '0.5947', '-0.06024', '0.284', '-0.5737', '0.01715', '0.1503', '-0.332', '0.1818', '-0.0454', '0.6333', '0.03885', '-0.0832', '0.1877', '-0.008606', '-0.2114', '0.6226', '-0.9937', '0.03052', '0.1725', '0.3623', '-0.2703', '0.2727', '0.136', '0.4224', '0.1943', '-0.06238', '-0.1161', '-0.75', '0.3257', '0.12396', '0.1015', '-0.175', '-0.3008', '0.3525', '0.2754']",C82342,,D006816,333.4,,10070668,
mondo:0007740,Wagner disease,"['Wagner disease (formerly)', 'hyaloideoretinal Degeneration of Wagner', 'VCAN-related vitreoretinopathy', 'WGVRP', 'Wagner syndrome', 'erosive vitreoretinopathy', 'WGN1', 'Wagner syndrome type 1', 'Wagner vitreoretinopathy', 'Wagner syndrome 1', 'Wagner vitreoretinal Degeneration', 'vitreoretinal degeneration, Wagner type', 'ERVR', 'dominant hyaloideoretinal dystrophy of Wagner']",,143200,898,C1840452,"['-0.3987', '-0.03613', '-0.6577', '0.3052', '-0.3103', '0.311', '-0.11774', '1.004', '-0.644', '-0.1907', '-0.02618', '-0.1209', '-0.6953', '-0.1676', '-0.203', '-0.3381', '-0.1364', '-0.1782', '0.049', '-0.675', '0.063', '0.082', '0.2175', '-0.1552', '-0.197', '-0.0837', '-0.512', '0.1733', '0.2123', '0.596', '0.8154', '-0.505', '0.3054', '-0.1282', '0.0925', '0.2878', '0.053', '-0.736', '-0.1418', '-0.8994', '0.303', '-0.1098', '0.3142', '0.0653', '-0.1481', '0.824', '-0.38', '-0.737', '-0.009346', '-0.0928', '1.145', '0.362', '0.2588', '-0.2322', '0.1702', '-0.187', '0.715', '-0.0965', '-0.1779', '0.2896', '0.698', '-0.1892', '0.01242', '0.5015', '-0.2568', '-0.865', '0.872', '0.7534', '0.0486', '0.04697', '-0.596', '0.3281', '0.05695', '-0.1464', '0.4858', '-0.212', '0.1089', '-0.0912', '-0.459', '0.01312', '0.03442', '-0.5117', '-0.0738', '1.12', '-0.4053', '0.0591', '0.2017', '0.3213', '-0.0761', '-0.1393', '0.1617', '0.3357', '0.1295', '0.6196', '1.359', '-0.1348', '0.0274', '-0.3445', '-0.3247', '0.1279']",,,C536075,,H35.5,10063383,
mondo:0007741,congenital hydronephrosis,,,,2190,C0266316,"['-0.1329', '-0.003458', '0.2069', '-0.0732', '0.08075', '0.0008173', '-0.1371', '0.3867', '-0.2822', '-0.03656', '-0.1664', '-0.2656', '-0.2106', '0.2764', '-0.4614', '-0.1559', '-0.05576', '0.00628', '0.03183', '-0.6675', '0.02812', '-0.07007', '0.257', '-0.1271', '0.2167', '-0.3035', '0.02332', '0.2922', '0.1864', '0.06036', '0.3125', '-0.3042', '0.2515', '0.1946', '-0.132', '-0.218', '0.0634', '0.1432', '0.0502', '-0.03897', '-0.1144', '-0.0688', '0.2393', '-0.10065', '-0.1337', '-0.1422', '-0.1173', '0.192', '0.00854', '0.1378', '-0.2756', '0.11816', '0.0878', '-0.2927', '-0.3037', '-0.1027', '0.2769', '-0.000965', '-0.3564', '0.05334', '0.3945', '0.03177', '-0.3206', '0.0722', '0.1298', '-0.1544', '0.3728', '0.357', '-0.2177', '0.09326', '-0.007378', '0.1351', '0.1653', '-0.08026', '-0.2644', '-0.1798', '0.11896', '0.01381', '-0.268', '-0.132', '-0.2329', '0.003876', '0.217', '0.1266', '-0.1313', '-0.03442', '0.1556', '-0.2131', '0.00118', '-0.158', '0.1661', '0.2096', '-0.1212', '-0.01797', '0.537', '0.05286', '0.434', '-0.2312', '0.0489', '0.3308']",C102979,,,753.29,Q62.0,10050975,
mondo:0007742,5-hydroxytryptamine oxygenase regulator,"['HTOR', '5-hydroxytryptamine oxygenase regulator', '5-HYDROXYTRYPTAMINE oxygenase regulator']",,143460,,,,,,,,,,
mondo:0007743,attention deficit-hyperactivity disorder,"['attention deficit-hyperactivity disorder', 'ADHD', 'attention deficit hyperactivity disorder', 'attention deficit/hyperactivity disorder']",,,,,,C97160,,,,,,
mondo:0007744,cholesterol-ester transfer protein deficiency,"['cholesterol ester transfer Protein deficiency', 'CETP deficiency', 'HALP1', 'high density lipoprotein cholesterol level quantitative trait locus 10', 'hyperalphalipoproteinemia', 'CEPT deficiency', 'hyperalphalipoproteinemia type 1', 'hyperalphalipoproteinemia 1', 'Hdlcq10', 'familial hyperalphalipoproteinemia', 'high density lipoprotein cholesterol level QTL 10']",0111369,143470,79506,CN205999,"['-0.0745', '0.0908', '0.002554', '0.0241', '0.0657', '-0.106', '-0.01458', '0.0817', '-0.0635', '-0.04105', '-0.0514', '0.01717', '0.0299', '0.00849', '-0.0592', '-0.07806', '-0.03214', '-0.02649', '-0.0688', '-0.1766', '-0.001778', '-0.1076', '0.1031', '0.02441', '0.02003', '-0.0361', '-0.0611', '-0.02351', '0.005302', '-0.06104', '0.0825', '0.03065', '0.11884', '0.01327', '0.00261', '-0.0909', '0.009', '-0.01595', '-0.00877', '-0.1274', '0.0539', '-0.1079', '0.0631', '-0.004612', '-0.05908', '-0.11163', '0.04474', '0.0525', '0.07623', '0.05997', '-0.04398', '-0.05627', '0.04254', '0.004513', '-0.06335', '-0.0322', '0.1603', '-0.0668', '-0.1442', '0.03004', '0.05148', '0.06058', '0.0463', '-0.02109', '0.05786', '0.03522', '0.0978', '0.05466', '-0.1004', '0.0887', '-0.08386', '0.01129', '-0.01098', '-0.0599', '0.05603', '0.0792', '0.02554', '0.006054', '-0.04138', '-0.04248', '0.01199', '-0.01283', '-0.03815', '0.05002', '0.02507', '0.01158', '0.05112', '0.07825', '0.164', '0.04453', '0.03824', '0.071', '-0.07117', '-0.0293', '0.1931', '0.114', '0.02968', '-0.1672', '-0.03044', '0.04852']",,,,,,,
mondo:0007745,Gilbert syndrome,"['Gilbert-Meulengracht syndrome', 'Gilbert^s disease', 'Gilbert syndrome', 'familial cholemia', 'hyperbilirubinemia, Gilbert type', 'hereditary nonhemolytic jaundice', 'hyperbilirubinemia type 1', 'Gilbert disease', 'constitutional hyperbilirubinemia', 'hyperbilirubinemia, Arias type', 'hyperbilirubinemia 1', 'Gilbert^s syndrome']",2739,143500,357,,"['-0.2379', '0.1683', '-0.2233', '0.1246', '-0.3596', '0.5063', '-0.716', '0.5435', '0.3584', '0.2052', '0.1687', '0.6763', '0.10406', '0.9507', '-0.2615', '-0.6123', '-0.4856', '0.3672', '0.0477', '-0.7534', '-0.0374', '-0.257', '0.2167', '0.04837', '0.04462', '0.005913', '0.0855', '-0.0676', '-0.000836', '-0.447', '0.6562', '0.2257', '-0.2443', '0.04697', '-0.3293', '0.4417', '-0.602', '-0.0898', '0.5312', '-0.7207', '0.1367', '0.3008', '-0.1423', '-0.1627', '-0.1757', '-0.4656', '0.2446', '-0.406', '0.4465', '0.3809', '-0.2732', '-0.3457', '0.04294', '0.3486', '-0.0894', '-0.2462', '0.2303', '0.298', '-0.2522', '-0.2952', '0.2', '0.399', '0.9893', '-0.1823', '-0.3286', '0.0867', '0.883', '0.089', '-0.409', '0.672', '-0.2295', '0.5513', '0.2218', '0.2478', '-0.05246', '0.6665', '0.2903', '0.4553', '0.3882', '0.1869', '0.2377', '0.087', '-0.0668', '-0.4128', '-0.0486', '-0.3113', '0.4429', '-0.2498', '0.7964', '0.0527', '0.44', '0.2542', '0.1609', '-0.2847', '0.8687', '0.5874', '-0.5474', '-0.513', '-0.2496', '-0.403']",C84729,0005556,D005878,,E80.4,,
mondo:0007746,"orthostatic hypotensive disorder, Streeten type","['OHDS', 'orthostatic hypotensive disorder', 'hyperbradykininism', 'orthostatic hypotensive disorder, Streeten type', 'orthostatic hypotensive disorder of Streeten']",,143850,,C1840438,,,,C564174,,,,
mondo:0007747,isolated hyperchlorhidrosis,"['hyperchlorhidrosis, isolated']",0111371,143860,542657,,"['-0.02502', '0.0279', '-0.00425', '0.002052', '0.01833', '-0.02232', '0.0049', '0.02808', '-0.02484', '-0.006607', '-0.00129', '-0.006252', '-0.0096', '0.01419', '-0.01078', '-0.01561', '-9.91e-05', '-0.02602', '-0.0243', '-0.0726', '-0.01082', '0.002167', '0.03323', '-0.01171', '0.01826', '0.00446', '-0.006718', '-0.008835', '0.00783', '-0.0166', '0.03137', '0.0009775', '0.01633', '0.006718', '0.01471', '-0.01301', '0.002151', '-0.001748', '-0.006996', '-0.03473', '0.01619', '-0.0376', '0.0146', '-0.013435', '-0.01384', '-0.0273', '-0.00972', '0.01675', '-0.003994', '0.03033', '-0.004997', '-0.002079', '-0.005188', '-0.004616', '-0.0329', '-0.008194', '0.0417', '-0.015274', '-0.04883', '0.001375', '0.01634', '0.01799', '0.0076', '0.001354', '-0.01264', '0.005135', '0.03485', '0.01313', '-0.03096', '0.02205', '-0.03041', '0.00788', '0.01252', '-0.02823', '0.010376', '0.02031', '0.001075', '-0.0007377', '-0.03174', '-0.0146', '0.00819', '-0.006145', '0.004936', '0.02971', '0.00954', '0.00215', '0.00469', '0.02852', '0.0425', '0.006645', '0.02052', '0.02533', '-0.004936', '0.0008354', '0.0697', '0.01617', '0.01665', '-0.0483', '-0.01683', '0.01233']",,,,276.9,,,
mondo:0007748,"hypercalciuria, absorptive, 2","['hypercalciuria, absorptive, type 2', 'hypercalciuria, absorptive, 2', 'hypercalciuria, absorptive, susceptibility to', 'hypercalciuria, familial idiopathic', 'HCA2']",,143870,,,,,,C562790,V18.19,,,
mondo:0007750,"hypercholesterolemia, familial, 1","['hypercholesterolemia, susceptibility to', 'hypercholesterolemia, familial', 'hyper-low-density-lipoproteinemia', 'FHC', 'low density lipoprotein cholesterol level quantitative trait locus 2', 'LDL receptor disorder', 'FHCL1', 'hypercholesterolemia, familial, modifier of', 'hyperlipoproteinemia, type 2', 'hyperlipoproteinemia, type 2A', 'LDL cholesterol level QTL2', 'hypercholesterolemia, familial, due to ldlr defect, modifier of', 'hypercholesterolemic xanthomatosis, familial']",,143890,,,,,,,,,,
mondo:0007751,"hypercholesterolemia, autosomal dominant, type B","['hypercholesterolemia, familial, due to ligand-defective apolipoprotein B', 'apolipoprotein B-100, familial defective', 'hypercholesterolemia, familial, 2', 'hypercholesterolemia, autosomal dominant, type B', 'apolipoprotein B-100, familial ligand-defective']",,144010,,,"['-0.015236', '0.0345', '-0.001273', '-0.01683', '0.007248', '-0.04105', '0.00595', '0.0376', '-0.02406', '-0.02808', '-0.012985', '-0.0002366', '0.01011', '0.005695', '-0.005856', '-0.02086', '-0.00481', '-0.004204', '-0.01155', '-0.0484', '-0.014496', '-0.02502', '0.02075', '-0.01376', '0.00605', '0.00376', '-0.00893', '-0.00963', '-0.001168', '-0.0211', '0.0372', '0.004494', '0.04208', '0.009514', '-0.002436', '-0.01289', '-0.02107', '-0.02432', '0.00635', '-0.03348', '0.006542', '-0.03214', '0.0155', '-0.0174', '-0.00494', '-0.04858', '-0.011856', '0.02386', '0.01011', '0.00312', '0.007378', '-0.01313', '0.01258', '-0.001451', '-0.00968', '-0.02115', '0.0313', '-0.001626', '-0.04114', '0.00249', '0.0158', '0.01003', '-0.003042', '0.0003579', '0.01155', '0.00636', '0.03864', '0.0378', '-0.03693', '0.04474', '-0.03964', '-0.006493', '-0.000426', '-0.01517', '0.01863', '0.02417', '0.001848', '0.00249', '-0.01874', '-0.0258', '0.000849', '0.00209', '-0.008194', '0.02507', '-0.00909', '0.01555', '0.01602', '0.02103', '0.04434', '0.003674', '0.01863', '0.03406', '-0.006096', '0.005352', '0.06366', '0.0307', '0.03854', '-0.03824', '0.0003886', '0.01839']",,,,,,,
mondo:0007752,hyperheparinemia,['hyperheparinemia'],,144050,,C3203346,,,,C562723,286.5,,,
mondo:0007753,Frey syndrome,"['HYPRG', 'Baillarger syndrome', 'hyperhidrosis, gustatory', 'Frey^s syndrome', 'auriculotemporal nerve syndrome', 'Frey syndrome', 'gustatory sweating', 'hyperhidrosis gustatory', 'gustatory hyperhidrosis']",11599,144100,,,,,1000940,D013547,,,,
mondo:0007754,hyperhidrosis palmaris ET plantaris,"['HYPRPP', 'hyperhidrosis, primary palmar', 'hyperhidrosis palmaris ET plantaris']",,144110,,C1274743,,,,C563185,,,,
mondo:0007755,hyperimmunoglobulin G1(A1) syndrome,"['hyperimmunoglobulin G1 syndrome', 'Immunoglobulin heavy chain regulator', 'hyperimmunoglobulin G1(A1) syndrome']",,144120,,C1840429,,,,C564173,,,,
mondo:0007756,hyperkeratosis lenticularis perstans,"['hyperkeratosis lenticularis perstans (disease)', 'hyperkeratosis lenticularis perstans of Flegel', 'hyperkeratosis lenticularis perstans', 'HLP', 'Flegel disease', 'Flegel^s disease']",,144150,409,C0263420,,,,C538377,,,10071311,0007570
mondo:0007757,hyperkeratosis-hyperpigmentation syndrome,['hyperkeratosis-hyperpigmentation syndrome'],,144190,1336,C1840428,,,,C564172,,,,
mondo:0007758,epidermolytic palmoplantar keratoderma,"['hyperkeratosis palmoplantar localized epidermolytic', 'epidermolytic palmoplantar keratoderma of VC6rner', 'hyperkeratosis, localised epidermolytic', 'hyperkeratosis palmoplantar localised epidermolytic', 'palmoplantar keratoderma, epidermolytic, with knuckle pads', 'palmoplantar keratoderma, Vorner type', 'diffuse erythrodermic palmoplantar keratoderma, Vörner type', 'hyperkeratosis, localized epidermolytic', 'diffuse erythrodermic palmoplantar keratoderma, Voerner type', 'keratosis palmaris Et plantaris Familiaris', 'keratosis of Greither', 'tylosis', 'epidermolytic palmoplantar keratoderma of Voerner', 'keratoderma, epidermolytic palmoplantar', 'EPPK', 'palmoplantar keratoderma, epidermolytic', 'Ppke', 'diffuse erythrodermic palmoplantar keratoderma, VC6rner type', 'epidermolytic palmoplantar keratoderma of Vörner']",0080223,144200,2199,C1721006,"['-0.2573', '0.10364', '0.0446', '0.0429', '0.2998', '-0.4546', '-0.1921', '-0.04102', '-0.1578', '-0.000666', '0.0005865', '0.1558', '-0.4314', '-0.2008', '-0.4585', '0.0639', '0.4517', '-0.5425', '0.02173', '-0.986', '-0.147', '-0.1665', '0.2585', '0.4387', '0.2698', '0.606', '-0.01881', '0.2754', '-0.0692', '-0.0822', '0.02512', '-0.2285', '-0.3154', '0.0671', '0.2512', '0.01379', '-0.2932', '0.0724', '0.2294', '-0.618', '-0.1555', '-0.4985', '-0.03314', '0.2369', '0.0425', '-0.3591', '-0.242', '0.323', '0.4578', '-0.2155', '-0.0536', '-0.1603', '0.1937', '0.1774', '-0.2489', '-0.4592', '0.66', '0.3853', '-0.5625', '-0.302', '-0.04977', '0.05847', '0.019', '-0.0698', '0.1589', '0.0674', '0.3528', '0.509', '0.2382', '0.7466', '-0.4885', '-0.1742', '0.3306', '0.4006', '0.075', '0.1794', '-0.06012', '0.3782', '-0.001525', '-0.351', '-0.06076', '-0.3203', '0.1816', '-0.03772', '0.0738', '-0.3806', '-0.0858', '0.7075', '0.1564', '0.2551', '0.11206', '0.335', '0.1426', '0.5757', '0.222', '0.1771', '0.358', '-0.646', '0.02005', '0.3093']",C84693,,,757.39,,,
mondo:0007759,"hyperlipidemia, familial combined, LPL related","['FCHL', 'combined hyperlipidemia, familial', 'hyperlipidemia, familial combined', 'familial combined hyperlipidemia']",,144250,,,,,,,,,,
mondo:0007760,"hyperlipoproteinemia, type II, and deafness","['hyperlipoproteinemia, type II, and deafness']",,144300,,C1840425,,,,C564170,,,,
mondo:0007762,hyperlipoproteinemia type V,"['type V hyperlipoproteinemia', 'mixed hyperlipemia', 'familial apolipoprotein a5 deficiency', 'familial hyperlipoproteinemia type V', 'familial APOA5 deficiency', 'hyperchylomicronemia, late-onset', 'HLP type 5', 'major hyperlipidemia', 'hyperlipemia, mixed', 'hyperlipemia mixed', 'hyperchylomicronemia with Hyperprebetalipoproteinemia, familial', 'familial type 5 hyperlipoproteinemia', 'hyperlipoproteinemia, type V', 'hyperlipidemia, type 5', 'hyperlipemia combined fat and carbohydrate-induced', 'hyperlipidemia type V', 'familial apolipoprotein A-V deficiency', 'hyperlipoproteinemia type 5', 'hyperlipemia, combined fat and carbohydrate-induced', 'hyperlipoproteinemia, type 5', 'hyperchylomicronemia late onset', 'Fredrickson type V lipaemia']",1171,144650,70470,,"['-0.08234', '0.257', '0.07117', '0.05145', '0.1313', '-0.1616', '-0.1808', '0.1396', '-0.1072', '0.06232', '-0.2595', '0.05453', '0.2844', '-0.1537', '-0.3433', '-0.2734', '0.2063', '-0.02408', '0.07745', '-0.3684', '0.0584', '-0.2472', '0.4087', '0.1355', '-0.01247', '0.2693', '0.1687', '-0.1327', '-0.0343', '-0.04044', '0.3438', '0.05658', '0.3496', '0.2194', '-0.0203', '-0.3633', '0.074', '-0.01588', '0.0105', '-0.5503', '-0.1969', '-0.2893', '0.2356', '0.0698', '-0.386', '-0.10315', '0.157', '0.269', '0.087', '0.135', '0.1769', '-0.1793', '0.0765', '-0.2703', '-0.1498', '-0.0697', '0.1385', '-0.482', '-0.37', '0.142', '-0.12036', '0.2405', '0.3347', '-0.315', '-0.03757', '0.1083', '0.1982', '0.04614', '-0.2656', '0.02495', '-0.2081', '-0.05377', '0.0458', '-0.1796', '0.2656', '0.1075', '-0.08386', '0.24', '-0.1669', '-0.1659', '-0.04492', '0.1753', '-0.12213', '0.0002444', '-0.04013', '0.10425', '0.01191', '0.2896', '0.4272', '-0.07794', '0.05624', '0.1219', '0.0912', '-0.1', '0.4353', '0.2219', '0.02415', '-0.6187', '-0.408', '0.08746']",,,D006954,,,10060755,
mondo:0007763,nonpapillary renal cell carcinoma,"['renal cell carcinoma, clear cell', 'RCC', 'renal cell carcinoma, nonpapillary', 'CCRCC', 'renal cell carcinoma, clear cell, somatic', 'adenocarcinoma of kidney', 'nonpapillary renal carcinoma 1 locus', 'renal cell carcinoma', 'renal cell carcinoma, somatic', 'clear cell renal cell adenocarcinoma', 'renal carcinoma, chromophobe, somatic', 'clear cell renal cell carcinoma', 'hypernephroma']",0050387,144700,,,"['-0.02353', '0.07263', '-0.002398', '0.01415', '0.01182', '-0.074', '0.012436', '0.1061', '-0.03354', '-0.04922', '-0.01778', '-0.0794', '-0.01554', '0.02258', '-0.1173', '-0.0731', '-0.00688', '-0.05377', '0.01671', '-0.1445', '-0.02266', '-0.08374', '0.0816', '-0.05426', '0.0866', '-0.05542', '-0.01115', '-0.011215', '-0.02522', '-0.059', '0.0912', '-0.01764', '0.1492', '0.000825', '0.009766', '-0.03946', '-0.03497', '-0.04648', '-0.0302', '-0.05698', '-0.01258', '-0.07556', '0.0441', '-0.0659', '-0.007427', '-0.0963', '-0.03384', '0.00835', '0.00143', '0.006023', '-0.00411', '0.00993', '0.04938', '0.013504', '-0.05725', '-0.03015', '0.08', '-0.01339', '-0.1536', '-0.01295', '0.08307', '0.03174', '-0.014275', '0.00985', '0.0311', '0.01191', '0.11084', '0.1069', '-0.0753', '0.1307', '-0.03262', '-0.03084', '0.005363', '-0.02324', '0.03604', '0.03906', '0.00976', '2.17e-05', '-0.04547', '-0.0574', '-0.0817', '0.05283', '-0.04636', '0.02142', '-0.0379', '-0.05368', '0.05743', '0.03168', '0.1346', '-0.000978', '0.0135', '0.0608', '-0.0117', '-0.03604', '0.1302', '0.0483', '0.06287', '-0.12177', '-0.02654', '0.04303']",,,,,,,
mondo:0007764,"autosomal dominant osteosclerosis, Worth type","['Ostéosclérose autosomique dominante type Worth', 'autosomal dominant endosteal hyperostosis', 'Worth^s syndrome', 'Van Buchem disease type 2', 'hyperostosis, endosteal', 'VBCH2', 'endosteal hyperostosis, autosomal dominant', 'hyperostosis corticalis generalisata, benign form of Worth with torus palatinus', 'osteosclerosis of the skull and enlarged mandible', 'hyperostosis corticalis generalisata, benign form of Worth, with torus palatinus', 'Worth syndrome', 'benign form of Worth hyperostosis corticalis generalisata with torus platinus', 'Van Buchem disease, type 2', 'osteosclerosis, autosomal dominant', 'osteosclerosis, autosomal dominant, Worth type', 'autosomal dominant osteosclerosis', 'endosteal hyperostosis, Worth type']",0080037,607636,2790,,"['-0.1603', '0.0644', '0.4324', '-0.615', '0.203', '-0.0322', '-0.10364', '0.827', '-0.2935', '-0.3884', '-0.05835', '-0.3638', '-0.237', '-0.444', '-0.05768', '0.2937', '0.254', '-0.3625', '-0.2427', '-0.59', '0.5605', '-0.1368', '0.518', '-0.1914', '0.1847', '0.299', '-0.0755', '-0.4163', '-0.1357', '-0.1555', '0.2164', '0.2827', '0.238', '-0.0797', '0.07587', '-0.2668', '-0.05612', '-0.432', '-0.05533', '-0.7036', '0.1453', '0.08856', '-0.10565', '0.0678', '-0.229', '-0.9556', '0.1775', '-0.05316', '0.4475', '-0.2043', '0.1389', '-0.0357', '0.4143', '0.11383', '-0.1257', '-0.7007', '0.08295', '0.418', '-0.1747', '0.266', '0.2617', '-0.3533', '-0.485', '-0.25', '0.1181', '-0.1846', '0.03287', '0.695', '-0.481', '0.4333', '-0.2047', '-0.03116', '0.013336', '-0.0079', '-0.04688', '0.0681', '-0.11115', '0.661', '0.2068', '-0.2603', '-0.04886', '-0.01097', '0.16', '0.526', '-0.364', '0.193', '0.00837', '0.03476', '0.02187', '0.4695', '-0.3608', '-0.128', '-0.307', '0.000148', '0.4841', '0.4077', '0.6895', '-0.1986', '-0.02551', '0.2435']",,,,,,,
mondo:0007765,hyperostosis cranialis interna,"['hyperostosis cranalis interna', 'hyperostosis cranialis interna', 'hyperostosis cranialis interna (disease)', 'HCIN']",,144755,443098,,"['-0.3433', '0.2367', '0.1383', '-0.1898', '-0.05893', '0.0196', '-0.1246', '0.6533', '-0.3154', '0.01776', '-0.396', '0.2465', '0.3132', '0.1306', '0.05942', '-0.2311', '0.281', '0.01967', '0.01287', '-0.6113', '-0.252', '-0.3364', '0.3613', '0.1418', '0.3748', '0.1238', '0.06052', '0.03568', '-0.07574', '0.507', '-0.006214', '0.01636', '0.1122', '-0.11255', '-0.2559', '-0.2441', '0.269', '-0.2725', '0.07513', '-0.1941', '-0.2573', '-0.1459', '0.2847', '-0.0845', '0.1783', '-0.2006', '0.1547', '0.1707', '0.0448', '0.0972', '0.3687', '0.3323', '0.1296', '-0.2004', '-0.00657', '-0.02386', '-0.2153', '-0.07465', '-0.02458', '0.1625', '-0.03748', '0.12256', '-0.2502', '0.077', '-0.2155', '-0.0002887', '0.3525', '0.5083', '-0.1295', '0.29', '-0.1008', '0.0958', '0.2279', '-0.4949', '0.3093', '0.06793', '0.2568', '0.589', '0.3464', '-0.1334', '-0.4531', '-0.05066', '0.2664', '0.2869', '-0.2493', '-0.1667', '-0.03973', '0.0165', '0.3823', '-0.2438', '-0.2278', '0.4126', '0.08905', '0.162', '0.3464', '0.4236', '0.3008', '-0.2017', '0.3115', '0.216']",,,C564168,,,,0005890
mondo:0007766,Morgagni-Stewart-Morel syndrome,"['Morgagni-Stewart-Morel syndrome', 'hyperostosis frontalis interna, obesity, shortness and cognitive impairment', 'MSM syndrome', 'hyperostosis frontalis interna']",,144800,77296,,,C84772,,D006957,,,,
mondo:0007767,hyperparathyroidism 1,"['HRPT1', 'hyperparathyroidism, familial primary', 'hyperparathyroidism 1', 'hyperparathyroidism type 1', 'parathyroid adenoma, familial', 'hyperparathyroidism, familial isolated primary']",,145000,99877,C1840403,"['-0.249', '0.1915', '-0.01996', '-0.07306', '0.1907', '0.2319', '-0.01259', '0.2142', '-0.08966', '-0.2079', '0.1355', '0.1788', '-0.012566', '-0.05502', '-0.3855', '-0.3103', '-0.092', '-0.08264', '-0.1354', '-0.6113', '0.09045', '-0.2388', '0.2937', '-0.04825', '0.3108', '-0.11194', '0.447', '-0.236', '0.0324', '-0.1641', '0.10077', '0.07965', '0.1835', '-0.1509', '-0.2996', '-0.1707', '-0.04398', '0.1572', '-0.0808', '-0.409', '0.1947', '-0.2202', '0.495', '-0.3835', '-0.02734', '-0.4348', '0.1034', '0.02045', '0.4595', '0.05243', '-0.05', '-0.1276', '0.1624', '0.1547', '-0.523', '-0.0586', '0.05106', '-0.09625', '-0.511', '0.2079', '0.6055', '0.03323', '0.1204', '-0.3015', '-0.05493', '0.1482', '0.3691', '0.541', '-0.3643', '0.07025', '-0.3599', '-0.015236', '0.2708', '0.0788', '-0.01302', '0.2208', '-0.003313', '0.3518', '-0.10406', '-0.1261', '-0.1783', '0.4658', '-0.0854', '-0.2917', '-0.2917', '-0.1166', '0.289', '-0.2703', '0.2854', '0.07745', '-0.01106', '0.2222', '-0.2024', '-0.2568', '0.4077', '0.0937', '0.307', '-0.4045', '-0.446', '0.2874']",,,,,,,
mondo:0007768,hyperparathyroidism 2 with jaw tumors,"['HPT-JT', 'hyperparathyroidism type 2', 'hyperparathyroidism-jaw tumour syndrome, hereditary', 'parathyroid adenoma with cystic changes', 'hyperparathyroidism-jaw tumor syndrome, hereditary', 'hyperparathyroidism 2 with jaw tumors', 'hyperparathyroidism-jaw tumor syndrome', 'parathyroid adenomatosis, familial cystic', 'hyperparathyroidism, familial primary, with multiple ossifying jaw fibromas', 'HRPT2', 'hereditary hyperparathyroidism-jaw tumor syndrome', 'hyperparathyroidism 2', 'hyperparathyroidism-2', 'hyperparathyroidism-jaw tumour syndrome', 'hereditary hyperparathyroidism-jaw tumour syndrome', 'familial primary hyperparathyroidism with multiple ossifying jaw fibromas']",,145001,99880,C1704981,"['0.5674', '-0.4883', '-0.3345', '0.1968', '-0.2627', '0.73', '-0.4607', '0.5854', '-0.3682', '0.0664', '0.2177', '-0.1327', '-0.4678', '0.4585', '-0.5635', '-0.2135', '-0.5425', '0.09906', '-0.68', '-1.079', '0.00386', '-0.7114', '0.365', '-0.4639', '0.626', '-0.201', '-0.026', '-0.5176', '0.2092', '0.0769', '0.623', '0.3132', '0.1353', '-0.1875', '-0.8516', '-0.3362', '-0.06976', '0.1199', '0.628', '0.04764', '0.1326', '-0.3188', '0.294', '-0.6855', '0.487', '-0.636', '-0.2416', '-0.0386', '0.7417', '-0.07526', '0.1967', '0.1512', '0.608', '0.07513', '-1.036', '0.007496', '-0.634', '0.1498', '-0.707', '0.2448', '0.5156', '-0.0086', '-0.512', '-0.302', '-0.4124', '0.553', '-0.0329', '1.025', '-0.2778', '0.1034', '0.33', '0.03696', '0.6553', '-0.135', '-0.09344', '0.1823', '-0.1464', '0.876', '0.9146', '0.5103', '-0.1365', '0.2318', '-0.011', '0.1064', '-0.08795', '-0.2393', '0.1866', '-0.2278', '1.028', '0.5034', '-0.1831', '0.2532', '-0.2227', '-0.688', '0.994', '-0.0834', '-0.2253', '-0.6235', '-0.02406', '0.3245']",C48287,,,,,,
mondo:0007769,hyperpigmentation of eyelid,"['dyspigmentation of eyelid', 'hyperpigmentation of eyelids']",10122,145100,,C0155211,,,1000711,C562400,374.52,,,
mondo:0007770,hyperpigmentation of Fuldauer and Kuijpers,['hyperpigmentation of Fuldauer and Kuijpers'],,145200,,C1840393,,,,C564164,,,,
mondo:0007771,"hyperpigmentation with or without hypopigmentation, familial progressive","['hyperpigmentation with or without hypopigmentation, familial progressive', 'hyperpigmentation, familial progressive, 2, formerly', 'hyperpigmentation, familial progressive, 2', 'melanosis universalis hereditaria', 'hyperpigmentation with or without hypopigmentation', 'melanosis, universal', 'FPHH', 'macules, hereditary congenital hypopigmented and hyperpigmented']",0111373,145250,,C1835039,"['-0.0611', '0.09094', '-0.01631', '-0.06287', '0.0763', '-0.09937', '-0.01053', '0.1159', '-0.125', '0.00189', '-0.0315', '-0.02528', '-0.0913', '0.02255', '-0.0763', '-0.0796', '0.03748', '-0.0985', '-0.04105', '-0.2494', '-0.02455', '-0.05542', '0.07214', '-0.010925', '0.0318', '0.02284', '-0.03653', '-0.04355', '0.01003', '-0.0669', '0.1272', '-0.02109', '0.1159', '0.04343', '0.01408', '-0.02693', '-0.09143', '-0.02187', '-0.02475', '-0.1317', '0.1261', '-0.1542', '0.04517', '-0.0176', '0.005653', '-0.08026', '-0.04233', '0.0545', '-0.01851', '0.0088', '-0.02843', '0.02303', '0.09503', '-0.01054', '-0.0276', '-0.04855', '0.08154', '-0.09607', '-0.2073', '-0.01988', '0.0663', '0.05692', '-0.004185', '-0.0007806', '0.01164', '-0.0256', '0.1577', '0.1881', '-0.076', '0.1602', '-0.09766', '-0.01212', '0.0461', '-0.10266', '0.05176', '0.02222', '0.01108', '-0.00787', '-0.03467', '-0.0772', '0.0647', '-0.0402', '-0.004864', '0.0499', '-0.03354', '-0.02367', '0.02954', '0.0956', '0.1664', '0.02493', '0.04663', '0.1168', '0.0243', '0.0529', '0.254', '-0.00791', '0.1323', '-0.121', '-0.001719', '0.0818']",,,,,,,
mondo:0007772,pseudohypoaldosteronism type 2A,"['hypertensive hyperkalemia, familial', 'hyperpotassemia and hypertension, familial', 'pseudohypoaldosteronism, type IIA', 'PHA2A', 'Gordon hyperkalemia-hypertension syndrome']",,145260,88938,C1840389,,,,,,,,
mondo:0007773,hyperproglucagonemia,"['glucagon, large molecular weight species of', 'hyperproglucagonemia']",,145270,,C1840388,,,,C564159,,,,
mondo:0007774,hyperreflexia,"['hyperreflexia', 'HRX', 'hyperreflexia (disease)']",,145290,,,,,,D012021,,,,0001347
mondo:0007775,"hypersecretion of adrenal androgens, familial","['familial hypersecretion of adrenal androgens', 'hypersecretion of adrenal androgens, familial']",,145295,,C1840387,,,,C536845,,,,
mondo:0007776,"hypersensitivity pneumonitis, familial","['hereditary hypersensitivity pneumonitis', 'hypersensitivity pneumonitis, familial']",,145300,,C1840386,,,,C536846,,,,
mondo:0007777,hypotaurinemic retinal degeneration and cardiomyopathy,['hypotaurinemic retinal degeneration and cardiomyopathy'],,145350,,C1840385,,,,C564157,,,,
mondo:0007781,"essential hypertension, genetic","['blood pressure regulation QTL', 'EHT', 'genetic essential hypertension', 'hypertension, essential, susceptibility to, 3', 'hypertension, essential, susceptibility to, 4', 'hypertension, essential, susceptibility to, 1', 'hypertension, salt-sensitive essential, susceptibility to', 'hypertension, essential, susceptibility to, 5', 'hypertension, essential, susceptibility to', 'hypertension, essential, salt-sensitive', 'hypertension, essential, susceptibility to, 6', 'hypertension, essential, susceptibility to, 2', 'hypertension, essential', 'hypertension, susceptibility to']",,145500,,,,,,,,,,
mondo:0007782,"hyperthermia, cutaneous, with headaches and nausea","['farmer syndrome', 'hyperthermia, cutaneous, with headaches and nausea']",,145590,,C1840373,,,,C564156,,,,
mondo:0007783,"malignant hyperthermia, susceptibility to, 1","['malignant hyperthermia of anaesthesia caused by mutation in RYR1', 'RYR1 malignant hyperthermia of anesthesia', 'King-Denborough syndrome', 'RYR1 malignant hyperthermia of anaesthesia', 'malignant hyperthermia, susceptibility to, 1', 'malignant hyperthermia susceptibility type 1', 'hyperpyrexia, malignant;MH KING syndrome, included', 'hyperthermia of anaesthesia', 'susceptibility to malignant hyperthermia 1', 'King syndrome', 'malignant hyperthermia of anesthesia caused by mutation in RYR1', 'malignant hyperthermia, susceptibility to, type 1', 'malignant hyperthermia susceptibility 1', 'King-Denborough syndrome, included', 'hyperpyrexia, malignant', 'MHS1', 'MHS', 'hyperthermia of anesthesia']",0080990,145600,99741,CN031421,"['-0.54', '-0.0211', '0.4407', '-0.569', '-0.0759', '-0.3872', '0.7686', '0.4038', '-0.2634', '-0.3145', '0.221', '0.4807', '0.263', '-0.3198', '-0.2737', '0.524', '-0.071', '-0.185', '-0.571', '-0.6826', '0.3608', '0.4001', '0.1903', '0.085', '-0.5845', '-0.2776', '-0.0938', '0.1719', '-0.06067', '-1.049', '0.354', '0.6177', '0.761', '0.0969', '-0.02637', '-0.457', '-0.368', '-0.3455', '0.2686', '-0.785', '-0.03366', '0.2', '0.323', '0.3372', '-0.2095', '-0.11145', '0.3086', '0.602', '0.04678', '0.3003', '-0.7197', '0.0708', '0.255', '0.666', '0.0531', '-0.4946', '-0.1882', '-0.2898', '0.177', '-0.05292', '0.459', '0.3657', '-0.4548', '0.3716', '-0.1692', '0.3057', '0.4116', '0.644', '-0.43', '0.5044', '-0.505', '0.3154', '0.4202', '0.1492', '0.355', '-0.04175', '0.1273', '-0.3503', '-0.1929', '-0.1317', '-0.08606', '0.09125', '-0.1438', '0.656', '-0.07556', '0.513', '-0.1225', '0.156', '0.4082', '-0.2471', '0.4492', '0.3975', '0.2118', '0.004967', '0.277', '0.2964', '0.3945', '-0.1033', '0.05048', '-0.1981']",,0009071,C535694,,,,
mondo:0007784,selective pituitary resistance to thyroid hormone,"['PRTH', 'pituitary resistance to thyroid hormone', 'thyroid hormone resistance, selective pituitary', 'hyperthyroidism, familial, due to inappropriate thyrotropin secretion']",0111374,145650,165994,C1840364,"['-0.63', '0.0719', '0.2117', '-0.1012', '0.1276', '0.03766', '0.361', '0.3735', '-0.1329', '-0.1803', '0.011086', '-0.1031', '0.05493', '-0.02414', '-0.04816', '-0.1256', '0.11957', '-0.0813', '-0.3552', '-0.505', '0.1475', '-0.0876', '0.1654', '-0.01292', '0.2588', '0.0975', '0.2302', '-0.1003', '0.1665', '-0.2457', '0.2108', '0.2338', '0.11285', '0.1389', '-0.2588', '-0.256', '-0.0349', '0.1512', '-0.03522', '-0.2029', '0.1626', '0.2263', '0.361', '-0.07', '0.1367', '-0.17', '0.2373', '0.1407', '-0.002924', '0.10535', '0.005882', '0.1216', '0.04724', '0.186', '-0.531', '0.4622', '0.3193', '-0.6655', '-0.298', '0.1187', '0.2412', '0.1439', '-0.2245', '-0.3867', '-0.2463', '0.2286', '0.2856', '0.594', '-0.4683', '0.1613', '-0.1946', '0.1755', '0.1831', '-0.3591', '0.1257', '-0.01903', '0.2305', '-0.2424', '-0.165', '-0.03146', '-0.2103', '0.3423', '0.01573', '0.00659', '-0.2452', '0.1093', '0.03192', '-0.07104', '0.507', '-0.0822', '0.2576', '0.2925', '0.00646', '-0.208', '0.694', '-0.2703', '-0.05707', '-0.1681', '-0.1444', '0.4497']",,,C564154,,,,
mondo:0007785,"hyperthyroxinemia, dystransthyretinemic","['hyperthyroxinemia, dystransthyretinemic', 'dystransthyretinemic hyperthyroxinemia', 'hyperthyroxinemia, Dysprealbuminemic', 'euthryroidal hyperthyroxinemia 2', 'DTTRH', 'dystransthyretinemic ethyroidal hyperthyroxinemia']",0080219,145680,,C2750824,,,,C567719,,,,
mondo:0007787,Ambras type hypertrichosis universalis congenita,"['congenital generalised hypertrichosis, Ambras type', 'congenital generalized hypertrichosis, Ambras type', 'hypertrichosis universalis congenita Ambras type', 'hypertrichosis, congenital generalized', 'hypertrichosis universalis congenita, Ambras type', 'Ambras syndrome', 'HTC 1', 'HTC1', 'hypertrichosis, congenital generalised']",0111060,145701,1023,C1840362,,,,,,,,
mondo:0007788,hypertriglyceridemia 1,"['hypertriglyceridemia, familial', 'hypertriglyceridemia, susceptibility to']",,145750,,,"['-0.01408', '0.03473', '-0.00774', '-0.01756', '0.00872', '-0.05545', '0.01066', '0.06042', '-0.0646', '0.003433', '-0.03085', '-0.004154', '-0.01688', '0.03436', '-0.05814', '-0.04428', '0.001356', '-0.01976', '-0.01475', '-0.1191', '0.02284', '-0.04407', '0.05627', '-0.02919', '0.0004356', '-0.003534', '0.01962', '-0.01846', '-0.005756', '-0.04514', '0.09766', '-0.01518', '0.0752', '0.02608', '-0.00941', '-0.02628', '-0.03586', '-0.02263', '-0.004116', '-0.06396', '0.010025', '-0.0638', '0.05145', '-0.0116', '0.01851', '-0.02113', '-0.0214', '0.0635', '-0.001376', '0.03897', '-0.007397', '0.002687', '0.03616', '-0.007015', '-0.03552', '-0.0175', '0.0552', '-0.05405', '-0.08124', '0.01239', '0.04752', '0.02682', '0.01277', '-0.0336', '-0.01941', '0.01524', '0.0779', '0.05017', '-0.06183', '0.0619', '-0.03223', '0.00902', '0.03296', '-0.03882', '0.03085', '0.04074', '0.001344', '0.021', '-0.027', '-0.05252', '-0.02477', '0.01079', '-0.0213', '0.0322', '0.004314', '0.02074', '0.01289', '0.04852', '0.09344', '-0.002703', '0.0362', '0.02333', '0.003386', '-0.0001281', '0.1236', '0.02606', '0.07697', '-0.0844', '-0.03854', '0.02129']",,,,,,,
mondo:0007789,hypertrophia musculorum vera,['hypertrophia musculorum vera'],,145800,,C1840361,,,,C564152,,,,
mondo:0007790,Charcot-Marie-Tooth disease type 3,"['Dejerine-Sottas syndrome', 'hereditary motor and sensory neuropathy type 3', 'HMSN III', 'Charcot-Marie-Tooth disease type 3', 'DSN', 'dejerine-sottas disease', 'hereditary motor and sensory neuropathy 3', 'hypertrophic neuropathy of Dejerine-Sottas', 'CMT3', 'Dejerine-Sottas neuropathy', 'HMSN3', 'hereditary motor and sensory neuropathy type III', 'Charcot-Marie-Tooth disease, type 3', 'hypertrophic neuropathy of infancy', 'HMSN 3']",0050540,145900,64748,C0011195,"['0.1606', '0.308', '0.126', '0.1105', '-0.2305', '-0.0989', '-0.492', '0.5156', '-0.748', '-0.04745', '-0.2244', '0.09406', '-0.3386', '-0.00481', '-0.05832', '-0.3064', '-0.06476', '-0.4246', '-0.3098', '-0.7285', '0.1444', '0.2394', '0.3706', '0.4133', '0.2507', '0.5645', '-0.1348', '0.2905', '0.0626', '-0.3254', '-0.04166', '-0.6753', '0.3635', '0.333', '0.1846', '-0.983', '-0.2008', '-0.1267', '0.1908', '-0.4219', '-1.65', '-0.2358', '-0.419', '0.3442', '-0.1628', '-0.2432', '0.205', '0.09973', '-0.236', '0.03714', '-0.03244', '0.3157', '-0.4624', '-0.9253', '0.3662', '-0.1964', '-0.01569', '0.2664', '-0.7104', '0.1599', '-0.2417', '0.10364', '0.9155', '1.068', '-0.744', '1.141', '-0.01672', '0.8604', '-0.5283', '0.2458', '-0.744', '-0.035', '0.262', '-0.07587', '1.344', '0.4746', '-0.594', '0.4116', '0.2314', '-0.4636', '0.2361', '0.259', '0.53', '0.713', '-0.07623', '-0.2247', '0.2361', '0.7256', '0.694', '0.2275', '0.3276', '-0.2267', '0.1113', '0.3726', '0.3801', '0.7886', '0.5034', '-0.651', '-0.1024', '0.2029']",C133087,,,,,,
mondo:0007791,familial hypocalciuric hypercalcemia 1,"['familial hypocalciuric hypercalcemia type 1', 'FHH type 1', 'familial hypocalciuric hypercalcemia type I', 'CASR familial hypocalciuric hypercalcemia', 'hpocalciuric hypercalcemia, type I', 'hypercalcemia, familial benign type 1', 'hypocalciuric hypercalcemia, familial, type 1', 'Fhh1', 'hypocalciuric hypercalcemia, familial, type I', 'HHC1', 'hypercalcemia, familial benign', 'hypocalciuric hypercalcemia type I', 'familial benign hypercalcemia type 1', 'familial hypocalciuric hypercalcemia caused by mutation in CASR', 'familial benign hypercalcemia 1', 'hypocalciuric hypercalcemia, acquired', 'FBH1']",0060700,145980,93372,,"['-0.04382', '0.0954', '0.7373', '0.0782', '-0.08374', '0.2754', '-0.0985', '0.5034', '-0.687', '-0.2046', '0.07214', '0.3235', '-0.89', '0.8774', '-0.05368', '-0.635', '-0.4297', '0.0958', '-0.03827', '-0.335', '0.6123', '-0.4902', '-0.3594', '-0.621', '0.785', '-0.417', '0.6904', '-0.759', '0.1254', '-0.4873', '-0.0505', '0.2269', '0.344', '-0.305', '-0.6733', '-0.6235', '-0.345', '0.1251', '0.1561', '-0.3354', '0.1173', '-0.3274', '0.2874', '-0.6665', '0.5537', '-0.4077', '-0.09033', '-0.11505', '0.2505', '0.625', '-0.2114', '0.6865', '0.5664', '-0.1332', '-0.7734', '0.1215', '-0.54', '0.721', '0.0229', '0.525', '0.6997', '0.2013', '0.00739', '-0.653', '-0.659', '0.3584', '0.0973', '0.632', '-0.3699', '0.1412', '0.1458', '0.5107', '0.2267', '-0.0685', '-0.09', '1.155', '-0.3408', '1.295', '0.744', '0.2627', '-0.7173', '-0.4543', '-0.00478', '-0.04852', '-0.05432', '-0.09814', '0.247', '0.1414', '0.8203', '0.389', '-0.004868', '0.2832', '-0.4446', '-0.4607', '0.8438', '0.8433', '0.2478', '-0.5605', '-0.577', '0.1188']",,,C537145,,,10068704,
mondo:0007792,familial hypocalciuric hypercalcemia 2,"['FHH type 2', 'hypocalciuric hypercalcemia, familial, type II', 'hypocalciuric hypercalcemia, familial, type 2', 'hypercalcemia, familial benign, type 2', 'hypercalcemia, familial benign type 2', 'FBH2', 'HHC2', 'hpocalciuric hypercalcemia, type II', 'familial benign hypercalcemia, type 2', 'hypocalciuric hypercalcemia type II', 'familial hypocalciuric hypercalcemia type 2']",0060701,145981,101049,C1840347,"['0.10095', '0.0617', '0.6924', '0.1492', '-0.045', '0.2164', '-0.3345', '0.4834', '-0.6846', '-0.0834', '0.09314', '0.2607', '-0.9775', '0.7217', '-0.2507', '-0.7856', '-0.6885', '0.1133', '-0.236', '-0.4446', '0.5483', '-0.4707', '-0.311', '-0.6133', '0.7476', '-0.5977', '0.4492', '-0.6353', '-0.02147', '-0.2766', '0.1132', '-0.04605', '0.446', '-0.3516', '-0.7183', '-0.734', '-0.512', '0.2025', '0.4753', '-0.4443', '0.0631', '-0.3318', '0.1877', '-0.545', '0.58', '-0.2852', '0.1517', '-0.0841', '0.1578', '0.6294', '-0.2883', '0.6924', '0.5986', '-0.1675', '-0.7886', '0.0719', '-0.5225', '0.5283', '-0.1025', '0.3052', '0.4285', '-0.03293', '0.04193', '-0.623', '-0.55', '0.2732', '0.1462', '0.6494', '-0.629', '0.2', '0.184', '0.421', '0.1371', '-0.2651', '-0.2338', '1.179', '-0.1621', '1.435', '0.842', '0.2146', '-0.6523', '-0.474', '-0.0401', '-0.03186', '0.231', '0.04504', '0.2362', '0.0928', '0.753', '0.629', '-0.227', '0.2028', '-0.657', '-0.3455', '0.6357', '0.99', '0.10974', '-0.3997', '-0.5522', '0.05655']",,,C537146,,,,
mondo:0007793,hypochondroplasia,"['hypochondroplasia', 'HCH']",0080041,146000,429,C0410529,"['0.06088', '0.3513', '0.2778', '-0.9824', '0.055', '-0.4175', '0.7134', '1.125', '-0.5806', '-0.4724', '0.2463', '0.1062', '0.1986', '0.5747', '0.3633', '-0.1116', '-0.0622', '-0.386', '-0.2173', '-0.5054', '-0.3115', '0.01851', '0.815', '-0.2168', '-0.639', '0.4224', '0.1252', '-0.2129', '0.1523', '-0.002539', '-0.03415', '-0.817', '-0.01073', '0.3901', '-0.1142', '-0.2448', '-0.2189', '-0.4668', '-0.01206', '0.1581', '-0.008125', '-0.0896', '0.2035', '0.266', '0.2678', '-0.2544', '-0.0485', '0.4685', '0.1833', '0.3657', '0.2002', '-0.375', '-0.32', '-0.09503', '-0.3855', '-0.6426', '-0.2842', '-0.2037', '0.159', '0.1395', '0.2413', '0.2908', '-0.4265', '-0.07837', '-0.323', '0.2197', '-0.1365', '0.3604', '-0.06104', '0.004467', '-0.0742', '0.1492', '0.2866', '-0.798', '-0.08966', '0.6484', '-0.1024', '-0.064', '-0.2996', '-0.4395', '0.464', '-0.284', '-0.4714', '0.532', '-0.0691', '0.4612', '0.274', '-0.3167', '0.5757', '0.53', '-0.000905', '-0.215', '-0.589', '0.461', '0.3337', '-0.5225', '0.6914', '-0.5093', '0.4265', '0.3916']",C118697,,C562937,756.9,Q77.4,10020967,
mondo:0007794,hypogonadotropic hypogonadism 7 with or without anosmia,"['hypogonadism, isolated hypogonadotropic', 'hypogonadotropic hypogonadism 7 without anosmia', 'idiopathic hypogonadotropic hypogonadism', 'hypogonadotropic hypogonadism 7 with or without anosmia', 'HH7']",0090078,146110,,,,,,,253.4,E23.0,,
mondo:0007795,mullerian duct anomalies-limb anomalies syndrome,"['limb-uterus syndrome', 'hypomelia with mullerian duct anomalies', 'Müllerian duct anomalies-limb anomalies syndrome', 'limb uterus syndrome', 'hypomelia mullerian duct anomalies', 'severe upper limb hypoplasia and Mullerian duct anomalies']",,146160,2491,C1840335,,,,C537155,,,,
mondo:0007796,"hypoparathyroidism, familial isolated 1","['FIH1', 'hypoparathyroidism familial isolated', 'hypoparathyroidism, familial isolated 1', 'FIH', 'hypoparathyroidism, autosomal dominant', 'hypoparathyroidism, familial isolated', 'hypoparathyroidism, autosomal recessive']",,146200,,,"['-0.01036', '0.0334', '0.00604', '0.003296', '0.00961', '-0.03616', '-0.00257', '0.0431', '-0.029', '-0.014946', '-0.00789', '-0.01378', '-0.001974', '0.006607', '-0.01209', '-0.02591', '0.006866', '-0.02147', '-0.01134', '-0.0537', '-0.0157', '-0.003944', '0.03073', '-0.01409', '0.0104', '0.00893', '-0.01168', '-0.01286', '0.02173', '-0.03223', '0.0197', '0.003714', '0.03946', '0.0247', '0.006668', '-0.003838', '0.001106', '-0.004482', '0.001644', '-0.02399', '0.012', '-0.02435', '0.013565', '-0.01125', '0.01897', '-0.02756', '-0.01275', '0.02533', '0.01225', '0.01495', '-0.006073', '-0.001396', '0.00899', '0.000707', '-0.02924', '-0.006454', '0.04477', '-0.02881', '-0.04742', '-0.001524', '0.03473', '0.004143', '0.00339', '-0.01735', '0.00817', '0.01507', '0.03986', '0.03117', '-0.0356', '0.04285', '-0.02911', '0.00716', '0.01918', '-0.031', '0.0172', '0.02617', '0.01973', '0.00855', '-0.01388', '-0.02097', '-0.01936', '-0.002123', '-0.01321', '0.01727', '0.011696', '-0.0187', '0.01118', '0.01453', '0.0563', '0.01131', '0.009', '0.01502', '-0.002453', '-0.00781', '0.089', '0.01564', '0.0351', '-0.04962', '-0.002827', '0.0125']",,,,,,,
mondo:0007797,hypoparathyroidism-deafness-renal disease syndrome,"['HDR syndrome', 'hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome', 'nephrosis, nerve deafness, and hypoparathyroidism', 'Barakat syndrome', 'hypoparathyroidism, sensorineural deafness, and renal dysplasia', 'hypoparathyroidism, deafness, and renal anomalies syndrome', 'hypoparathyroidism, sensorineural deafness, and renal disease', 'HDR']",0060878,146255,2237,C1840333,"['0.227', '-0.0726', '-0.2496', '0.1202', '-0.9526', '0.4958', '-0.03796', '0.8965', '-0.865', '-1.253', '-0.2131', '-0.12274', '-0.3518', '0.5215', '-0.2668', '0.3176', '0.1133', '-0.2903', '0.09674', '-0.317', '0.2075', '-0.1566', '-0.3875', '-0.2081', '0.2698', '-0.4016', '-0.2703', '-0.3354', '0.6504', '-0.703', '0.02277', '0.0422', '-0.109', '-0.1287', '-0.045', '-0.3616', '-0.0866', '-0.04636', '0.5854', '0.3044', '0.0732', '0.3438', '0.826', '-0.641', '0.6313', '-0.914', '0.221', '0.02141', '-0.5347', '0.2693', '0.1321', '0.4412', '0.9707', '-0.2786', '-0.652', '-0.4382', '-0.1588', '-0.817', '-0.3425', '-0.1927', '-0.2042', '-0.774', '0.1417', '-0.05273', '-0.2222', '0.613', '0.6816', '0.91', '-0.5854', '-0.0773', '-0.1871', '-0.4448', '0.3003', '-0.3054', '0.369', '0.0661', '0.6772', '0.293', '0.311', '0.1993', '0.4202', '0.3613', '0.11975', '-0.4966', '-0.1543', '-0.829', '-0.1439', '0.4343', '0.2328', '0.2263', '0.0677', '0.3213', '-0.3352', '-0.401', '0.592', '-0.04074', '0.2612', '-0.945', '0.2322', '0.2397']",C130983,,C537907,,,,
mondo:0007799,hypophosphatemic bone disease,"['hypophosphatemic bone disease', 'HBD']",,146350,,C1840321,,,,C564145,,,,
mondo:0007800,chromosome 18p deletion syndrome,"['De Grouchy syndrome', '18p-', 'chromosome 18p deletion', 'chromosome 18p deletion syndrome', 'monosomy type 18p', 'partial deletion of chromosome 18p', 'partial deletion of the short arm of chromosome type 18', 'partial monosomy of the short arm of chromosome 18', 'monosomy 18p', 'partial monosomy of chromosome 18p', 'deletion 18p syndrome', '18p syndrome', 'partial deletion of the short arm of chromosome 18']",0060406,146390,261974,C0432442,,C84521,,C538309,758.39,,,
mondo:0007802,"hypospadias 3, autosomal","['hypospadias 3, autosomal, multifactorial', 'HYSP3', 'hypospadias 3, autosomal']",,146450,,C2675154,,,,C567191,,,,
mondo:0007803,multiple system atrophy,"['autonomic failure, Pure', 'hypotension, orthostatic', 'susceptibility to multiple system atrophy 1', 'multisystem atrophy', 'Shy-Drager syndrome', 'MSA', 'Shy-dragger syndrome (formerly)']",4752,,102,C0393571,"['0.2042', '0.3188', '-0.669', '0.3467', '-0.7456', '-0.2238', '0.4536', '0.9688', '-0.3398', '-0.01358', '-0.03754', '-0.0756', '-0.7754', '-0.01167', '0.3467', '-0.3152', '-0.469', '-0.3425', '-0.12146', '-0.3164', '-0.1306', '-0.324', '0.4292', '0.163', '0.2622', '-0.04395', '0.02162', '-0.0648', '-0.1663', '0.2106', '0.3804', '0.1505', '0.874', '-0.2458', '-0.2852', '-0.2308', '-0.2231', '0.4246', '0.2751', '-0.296', '0.67', '-0.2454', '-0.3564', '-0.072', '0.684', '-0.515', '-0.1816', '0.03125', '-0.1637', '0.139', '-0.258', '0.6514', '-0.364', '-0.881', '-0.10803', '-0.145', '0.378', '0.08673', '0.06223', '-0.889', '0.11365', '0.407', '-0.3474', '0.3298', '-0.785', '0.175', '0.3545', '0.3286', '-0.3916', '0.3313', '-0.4905', '-0.0545', '-0.11383', '-0.2081', '0.1313', '0.1093', '0.0675', '0.4548', '-0.1799', '0.0682', '0.0478', '-0.8335', '0.728', '0.2898', '-0.02055', '0.3098', '0.3384', '0.05414', '0.7124', '0.0807', '0.07245', '-0.1995', '-0.2324', '0.2281', '-0.061', '0.4548', '-0.2094', '0.1425', '0.1674', '0.4756']",C84909,1001050,D019578,,,10064060,
mondo:0007804,Pallister-Hall syndrome,"['Pallister Hall syndrome', 'Pallister-Hall syndrome', 'ano-cerebro-digital syndrome', 'hypothalamic hamartoblastoma, hypopituitarism, imperforate anus, and postaxial polydactyly', 'PHS', 'hypothalamic hamartoblastoma syndrome']",9248,146510,672,C0265220,"['-0.1418', '0.2458', '-0.0857', '-0.8086', '0.1277', '-0.1033', '0.02573', '0.06213', '-0.4946', '-0.9937', '-0.05582', '-0.6113', '0.0941', '-0.03717', '-0.2883', '-0.06866', '0.4133', '-0.9424', '-0.159', '-0.6416', '0.1665', '-0.0696', '0.982', '-0.10315', '0.04663', '-0.3762', '-0.11127', '-0.0374', '0.8525', '-0.683', '0.3604', '-0.415', '0.3108', '-0.1967', '0.05136', '-0.3486', '-0.11707', '-0.3562', '-0.06866', '0.3757', '0.3591', '0.2932', '0.727', '0.0832', '0.221', '-0.6147', '-0.1497', '0.5923', '0.08185', '0.3044', '-0.0715', '0.03848', '0.0289', '-0.03937', '-0.01259', '-0.2534', '0.509', '-0.1725', '0.174', '0.3784', '0.7305', '0.572', '-0.5967', '0.0462', '-0.2219', '0.4255', '-0.08844', '0.347', '-0.1262', '0.06207', '-0.5015', '0.01566', '-0.05908', '-0.0393', '-0.10815', '0.1699', '0.8364', '-0.3728', '-0.4402', '0.4436', '-0.1407', '0.736', '0.1428', '0.03854', '-0.4365', '0.419', '0.341', '0.4263', '-0.06824', '-0.3179', '-0.2551', '-0.3289', '-0.0716', '0.2834', '0.487', '0.2556', '0.3303', '-0.365', '0.5566', '0.8613']",C84987,,D054975,759.89,,,
mondo:0007805,hypotrichosis 2,"['Spanish type hypotrichosis', 'Htss', 'hypt2', 'hypotrichosis type 2', 'hypotrichosis, Spanish type', 'CDSN hypotrichosis', 'hypotrichosis caused by mutation in CDSN', 'hypotrichosis 2', 'hypotrichosis simplex of the scalp 1', 'HYPT2']",0110699,146520,,,,,,C564143,,,,
mondo:0007807,hypoxanthine guanine phosphoribosyltransferase suppressor,['hypoxanthine guanine phosphoribosyltransferase suppressor'],,146580,,,,,,,,,,
mondo:0007808,ichthyosis hystrix of Curth-Macklin,"['ichthyosis hystrix, Curth Macklin type', 'ichthyosis hystrix, Curth-Macklin type', 'IHCM', 'ichthyosis histrix, curth-macklin type', 'Curth-Macklin type ichthyosis hystrix', 'ichthyosis HYSTRIX, Curth-Macklin type']",,146590,79503,C1840296,"['-0.03635', '0.01965', '-0.3513', '-0.437', '-0.3342', '-0.6914', '-0.2064', '-0.01958', '-0.2615', '-0.281', '-0.1986', '0.3242', '-0.4182', '-0.0341', '-0.0323', '0.06055', '0.4768', '-0.7334', '0.03293', '-1.004', '-0.4495', '-0.10535', '0.61', '-0.526', '0.007504', '0.536', '-0.4675', '0.2778', '-0.1655', '-0.0351', '-0.0728', '0.004025', '-0.2986', '-0.02545', '0.08466', '-0.1042', '-0.02026', '-0.2477', '0.391', '0.4448', '0.1997', '-0.536', '0.05783', '-0.1217', '0.1107', '0.05328', '-0.3748', '0.2473', '0.0737', '-0.3896', '0.11835', '-0.1914', '0.708', '-0.0763', '-0.7886', '0.218', '0.7456', '0.06885', '-0.3118', '-0.09863', '-0.12494', '0.003275', '-0.5884', '-0.2712', '0.2367', '0.065', '0.616', '0.375', '0.06198', '0.714', '-0.137', '-0.1819', '0.1783', '-0.2744', '0.2295', '-0.3098', '-0.4097', '-0.3196', '-0.0433', '-0.3076', '0.00011927', '-0.4236', '0.1565', '0.4565', '0.3296', '0.02892', '-0.1462', '0.3696', '0.3525', '0.4702', '0.5713', '0.25', '0.4453', '0.8174', '0.4966', '0.2322', '0.3113', '-0.554', '0.364', '0.2104']",,,C536088,757.39,,,
mondo:0007809,"ichthyosis histrix, Lambert type","['Lambert type ichthyosis', 'ichthyosis, Lambert type', 'porcupine Man', 'ichthyosis hystrix gravior']",,146600,79504,,,,,C536087,757.39,Q80.0,,
mondo:0007810,autosomal dominant ichthyosis vulgaris,"['ichthyosis vulgaris', 'ichthyosis simplex', 'dominant congenital ichthyosiform erythroderma', 'ichthyosis vulgaris, autosomal dominant', 'dominant ichthyosis vulgaris']",1702,146700,462,C0079584,,C84778,,,,Q80.0,,
mondo:0007811,ichthyosis-cheek-eyebrow syndrome,"['ichthyosis cheek eyebrow syndrome', 'ichthyosis--cheek--eyebrow syndrome', 'Sidransky-Feinstein-Goodman syndrome', 'Sidransky Feinstein Goodman syndrome', 'Ice syndrome']",,146720,2267,,,,,C536084,,,,
mondo:0007812,"ichthyosis, lamellar, autosomal dominant","['lamellar ichthyosis, autosomal dominant', 'ichthyosis, lamellar, autosomal dominant', 'ichthyosis lamellar, autosomal dominant']",,146750,,,,,,C537263,,,,
mondo:0007813,superficial epidermolytic ichthyosis,"['ichthyosis bullosa of Siemens', 'bullous type of ichthyosis', 'superficial epidermolytic ichthyosis', 'bullous type ichthyosis', 'ichthyosis, bullous type', 'SEI', 'IBS', 'ichthyosis exfoliativa']",0060877,146800,455,C0432306,"['-0.1283', '0.2001', '-0.9194', '-0.304', '0.1674', '-0.2805', '-0.2605', '0.2413', '0.334', '-1.102', '-0.1968', '0.1906', '-0.2097', '0.313', '-0.258', '0.466', '0.3184', '-0.6943', '-0.05133', '-1.238', '0.0081', '0.09937', '0.977', '0.06033', '-0.3823', '0.4915', '-0.4595', '0.3572', '-0.654', '-0.3596', '0.2507', '0.0787', '-0.3699', '0.4158', '-0.3735', '0.2241', '-0.566', '-0.4216', '-0.1283', '0.1307', '0.3115', '-0.6', '-0.2847', '0.2428', '0.05334', '0.02626', '-0.0746', '-0.0968', '0.432', '-0.02357', '0.03793', '-0.609', '0.2578', '0.0191', '-0.7905', '0.2878', '0.8174', '0.2341', '-0.1177', '-0.4424', '-0.2365', '0.4426', '-0.654', '-0.795', '0.2935', '0.2175', '0.776', '0.6626', '0.1714', '0.734', '-0.09357', '-0.0806', '0.7617', '0.1572', '0.358', '0.2988', '-0.2861', '0.0158', '0.5913', '-0.4429', '-0.2021', '0.1305', '0.1407', '0.01761', '0.07776', '0.2223', '-0.01878', '0.09863', '0.3342', '0.247', '0.4902', '0.00928', '0.2441', '0.906', '0.1731', '0.608', '0.315', '-0.4448', '0.0657', '0.05505']",C84777,,D053560,,,,
mondo:0007814,"immune deficiency, familial variable","['immune deficiency, familial variable']",,146830,,C1840266,,,,C564136,,,,
mondo:0007817,"IgE responsiveness, atopic","['IGER', 'type 1 hypersensitivity reaction', 'IgE responsiveness, atopic', 'type I hypersensitivity', 'IgE response underlying allergic asthma and rhinitis', 'IgE, elevated level of', 'type I immediate hypersensitivity reaction', 'immediate hypersensitivity', 'IgE responsiveness, ATOPIC', 'Immunoglobulin E, basic level of, in serum', 'atopy, susceptibility to', 'IgE, level of', 'type 1 hypersensitivity', 'type I hypersensitivity reaction', 'Atopic hypersensitivity']",,147050,,C1840253,"['-0.0677', '0.08734', '0.02725', '-0.02817', '0.0106', '-0.0691', '0.0497', '0.0669', '-0.07214', '-0.00345', '-0.04642', '0.00805', '-0.04123', '0.00819', '-0.03888', '-0.02647', '0.05148', '-0.0115', '-0.0376', '-0.1967', '-0.0724', '-0.04306', '0.10046', '-0.027', '0.05295', '-0.005795', '-0.001751', '0.0286', '-0.0228', '-0.0992', '0.0909', '-0.013756', '0.1305', '0.0905', '0.004402', '-0.02556', '-0.02663', '-0.01097', '-0.03485', '-0.1254', '0.06033', '-0.07837', '0.04395', '0.002386', '0.0042', '-0.07513', '0.03427', '0.068', '-0.0246', '0.0828', '-0.04517', '-0.05075', '0.01445', '0.02567', '-0.0544', '0.05936', '0.07166', '-0.06384', '-0.0843', '0.01046', '0.01819', '0.0897', '-0.0339', '0.02689', '0.05432', '-0.00952', '0.1306', '0.05914', '-0.04486', '0.1406', '-0.0796', '0.008545', '0.03622', '-0.0859', '-0.001268', '-0.01634', '0.03317', '-0.0439', '-0.0005865', '-0.02069', '0.01796', '-0.02298', '-0.056', '0.07733', '-0.03207', '0.007244', '0.00975', '0.07104', '0.1229', '-0.01467', '0.01439', '0.0858', '-0.02669', '0.0214', '0.1844', '0.06094', '0.04004', '-0.10126', '-0.04077', '0.01878']",C3116,,C564133,,,,
mondo:0007818,"hyper-IgE recurrent infection syndrome 1, autosomal dominant","['hyperimmunoglobulin E syndrome type 1', 'HIES autosomal dominant', 'HIES, autosomal dominant', 'immunodeficiency with defective leukocyte and lymphocyte function and with response to histamine-1 antagonist', 'autosomal dominant HIES', 'AD-HIES', 'autosomal dominant hyperimmunoglobulin E syndrome', 'hyper-IgE syndrome, autosomal dominant', 'JOB syndrome', 'hyperimmunoglobulin E recurrent infection syndrome, autosomal dominant', 'autosomal dominant hyper IgE syndrome', 'Job^s syndrome', 'autosomal dominant hyper-IgE syndrome', 'hyper-IgE recurrent infection syndrome', 'STAT3 deficiency', 'hyper Ig E syndrome, autosomal dominant', 'hyper-IgE recurrent infection syndrome, autosomal dominant', 'AD hyperimmunoglobulin E syndrome', 'Job syndrome autosomal dominant', 'hyperimmunoglobulin E-recurrent infection syndrome', 'Buckley syndrome']",3261,147060,2314,C1968689,"['0.2522', '0.02841', '-0.2467', '-0.3647', '0.01743', '0.2585', '0.5176', '0.461', '-0.6133', '0.4062', '-0.2288', '0.00702', '-0.1786', '-0.5854', '-0.4072', '0.2386', '0.233', '0.648', '-0.1621', '-0.6655', '0.05243', '-0.243', '0.512', '0.146', '-0.2615', '0.06335', '0.009514', '0.0955', '0.4885', '-0.301', '0.5645', '0.05603', '0.3054', '-0.0921', '-0.02795', '-0.2307', '0.1252', '-0.1613', '0.259', '-0.352', '0.32', '0.303', '0.32', '-0.1672', '0.1902', '-0.0739', '0.359', '0.1004', '-0.08624', '-0.2137', '0.3503', '-0.05203', '0.573', '-0.2278', '-0.771', '-0.3296', '0.1729', '-0.4844', '0.4072', '-0.199', '0.4272', '0.5166', '-0.1437', '0.0754', '0.7407', '-0.02414', '0.1267', '0.3738', '-0.438', '0.948', '-0.2186', '-0.03888', '-0.1272', '-0.06934', '0.3508', '-0.007835', '0.3228', '-0.0945', '0.66', '-0.1809', '-0.4678', '-0.3171', '0.05127', '0.72', '-0.4492', '0.6587', '-0.12463', '0.313', '0.0719', '-0.108', '-0.04745', '0.1765', '-0.004112', '0.0256', '0.833', '0.6743', '0.4583', '-0.548', '-0.2257', '0.03818']",C126342,0003775,C567925,,,,
mondo:0007819,solitary median maxillary central incisor syndrome,"['solitary MEDIAN maxillary central incisor', 'single central maxillary incisor', 'SMMCI syndrome', 'SMMCI', 'single upper central incisor', 'incisors, Fused', 'solitary median maxillary central incisor syndrome', 'single median maxillary central incisor', 'incisors fused', 'Fused incisors']",,147250,2286,,"['-0.1992', '0.312', '0.2312', '-0.2473', '0.1323', '0.1713', '-0.0318', '0.2402', '-0.2532', '-0.1554', '-0.1984', '-0.05994', '-0.07306', '-0.02321', '0.036', '0.1292', '0.1995', '-0.1969', '-0.3', '-0.3254', '-0.1113', '-0.10657', '0.07526', '-0.1406', '0.3298', '0.09344', '-0.1161', '-0.11816', '0.1738', '-0.508', '0.325', '0.1738', '0.08813', '0.03375', '0.2257', '-0.01863', '0.2712', '-0.4028', '-0.1191', '-0.144', '-0.03494', '-0.2893', '0.2869', '-0.11163', '-0.0819', '-0.1824', '0.0853', '-0.0668', '0.10126', '0.1392', '0.04', '-0.1823', '-0.394', '0.2646', '-0.4722', '-0.12317', '0.3606', '-0.2443', '-0.2446', '0.2031', '0.1084', '-0.1664', '-0.2487', '0.1934', '-0.03568', '0.0125', '0.2717', '0.51', '-0.1908', '0.202', '-0.2263', '0.1505', '0.4678', '-0.1704', '0.0814', '0.1061', '-0.00863', '0.1802', '-0.346', '-0.1316', '-0.1307', '0.0907', '-0.006245', '0.1864', '-0.1092', '0.03108', '-0.05582', '0.1967', '0.11304', '-0.0995', '-0.1278', '0.2595', '0.07837', '0.0417', '0.762', '-0.2238', '0.3845', '-0.5146', '0.1499', '0.137']",,,C537342,,,,
mondo:0007820,fused mandibular incisors,"['Double tooth', 'incisors, FUSED mandibular', '^Double Tooth^']",,147251,2287,CN201433,,,,,,,,
mondo:0007824,"incisors, lower central, absence of","['incisors, lower central, absence of']",,147330,,,,,,,,,,
mondo:0007825,"incisors, rotation of upper central","['incisors, rotation of upper central']",,147350,,,,,,,,,,
mondo:0007826,"incisors, shovel-shaped","['Sinodonty', 'incisors, shovel-shaped']",,147400,,,,,,,,,,
mondo:0007827,inclusion body myositis,"['inclusion body myositis', 'sporadic inclusion body myositis', 'inflammatory myopathy', 'Ibm', 'IBM', 'sIBM']",3429,147421,611,C0238190,,C84786,0007323,D018979,729.1,,10066407,
mondo:0007828,"indifference to pain, congenital, autosomal dominant","['insensitivity to pain, congenital, autosomal dominant', 'Marsili syndrome', 'MARSIS', 'congenital analgesia, autosomal dominant', 'indifference to pain, congenital, autosomal dominant', 'MARSILI syndrome']",0081075,147430,,C1840219,,,,C564128,,,,
mondo:0007829,"cholestasis, intrahepatic, of pregnancy, 1","['ICP1', 'cholestasis, intrahepatic, of pregnancy, 1', 'cholestasis, pregnancy-related, 1', 'cholestasis, intrahepatic, of pregnancy, type 1']",0070228,147480,,C3549845,,,,,,,,
mondo:0007830,insensitivity to pain with hyperplastic Myelinopathy,['insensitivity to pain with hyperplastic Myelinopathy'],,147530,,,,,,,,,,
mondo:0007831,"insect Stings, hypersensitivity to","['insect Stings, hypersensitivity to']",,147540,,,,,,,,,,
mondo:0007832,interferon antiviral depressor,['interferon antiviral depressor'],,147560,,,,,,,,,,
mondo:0007833,"iris pigment layer, cleavage of","['iris pigment layer, cleavage of']",,147610,,,,,,,,,,
mondo:0007834,islet cell adenomatosis,"['INSULINOMATOSIS and diabetes mellitus', 'Insulinomatosis and diabetes mellitus', 'nesidioblastosis', 'islet cell adenomatosis', 'INSDM']",,147630,,C1578917,"['-0.0178', '0.02179', '0.01299', '0.004883', '0.00901', '-0.02617', '0.01904', '0.0466', '-0.01727', '-0.0215', '-0.00977', '-0.002926', '0.0004', '0.003664', '-0.02457', '-0.0344', '-0.002817', '-0.01415', '-0.006657', '-0.0603', '-0.006817', '-0.03091', '0.02844', '-0.00982', '0.01142', '-0.01958', '-0.008286', '-0.00682', '-0.00604', '-0.01281', '0.03918', '-0.01379', '0.04123', '-0.001092', '-0.008545', '-0.01747', '-0.003967', '-0.01634', '-0.01331', '-0.02504', '0.006138', '-0.03137', '0.02667', '-0.02057', '-0.001498', '-0.03284', '-0.01695', '-9.76e-05', '0.01028', '0.00529', '-0.00756', '0.008125', '0.0005827', '0.01962', '-0.02487', '-4.93e-05', '0.0303', '-0.0239', '-0.0417', '0.01486', '0.02675', '0.02272', '-0.01624', '0.01464', '-0.003193', '0.011345', '0.02669', '0.03223', '-0.01266', '0.05194', '-0.01482', '-0.011696', '-0.00548', '-0.0272', '0.02141', '0.01307', '0.002565', '-0.002594', '-0.00921', '-0.01459', '-0.02148', '0.00784', '-0.01022', '0.01657', '-0.02512', '-0.008354', '0.0018215', '0.0288', '0.04642', '-0.00486', '0.01682', '0.02493', '-0.00395', '-0.01301', '0.0725', '0.02702', '0.0179', '-0.05234', '-0.02238', '0.01008']",C4375,,C563258,,,,
mondo:0007835,intussusception,"['intussusception (morphologic abnormality)', 'intussusception of intestine', 'invagination of intestine or colon', 'intussusception']",8446,147710,,C0021933,,,,D007443,560.0,K56.1,,
mondo:0007836,IVIC syndrome,"['Instituto venezolano de Investigaciones Cientificas syndrome', 'oculootoradial syndrome', 'IVIC syndrome', 'OORS', 'radial ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia', 'radial Ray defects, hearing impairment, external ophthalmoplegia, and thrombocytopenia', 'oculo-oto-radial syndrome']",0111381,147750,2307,C1327918,"['0.07764', '-0.11816', '-0.3296', '-0.03946', '0.05933', '-0.6475', '0.33', '0.5015', '-0.1676', '-0.271', '0.03894', '-0.5415', '-0.7617', '-0.0635', '0.2075', '0.1313', '-0.2454', '-0.4207', '-0.3198', '-0.2324', '0.4226', '0.3025', '0.4548', '-0.2932', '0.648', '0.578', '-0.0243', '0.06168', '0.658', '-0.143', '0.2732', '0.144', '-0.0711', '-0.3135', '0.2245', '-0.911', '0.046', '-0.616', '-0.362', '-0.1829', '-0.1299', '-0.4243', '0.1799', '-0.2769', '0.2145', '-0.3406', '-0.0696', '0.3267', '-0.0279', '0.511', '0.002058', '-0.4568', '-0.312', '-0.1886', '-0.6846', '-0.7446', '0.3008', '-0.6694', '-0.1262', '-0.01733', '-0.05035', '-0.526', '0.3696', '0.1283', '-0.92', '-0.4167', '-0.1464', '0.715', '-0.476', '0.1494', '-0.6562', '0.0823', '-0.121', '0.2266', '0.5234', '0.3289', '-0.1345', '0.10046', '0.1126', '-0.1809', '-0.1295', '0.11847', '0.5513', '0.815', '-0.1656', '0.2455', '0.05457', '0.3389', '0.2468', '-0.4067', '-0.179', '0.2471', '0.2401', '0.187', '0.736', '0.2854', '0.6616', '-0.5522', '0.4685', '0.2008']",,,C535544,,,,
mondo:0007837,Johnson neuroectodermal syndrome,"['alopecia-anosmia-deafness-hypogonadism syndrome', 'alopecia-anosmia-conductive hearing loss-hypogonadism syndrome', 'alopecia anosmia deafness hypogonadism syndrome', 'Johnson-McMillin syndrome', 'Johnson neuroectodermal syndrome', 'Aadh syndrome']",,147770,2316,C0796002,,,,C535882,,,,
mondo:0007838,Jacobsen syndrome,"['Jacobsen syndrome', 'JBS', '11q terminal deletion disorder', 'distal monosomy 11q', 'distal deletion 11q', 'Jacobsen syndrome, Isolated cases', 'Del(11)(qter)', 'Del(11)(q23.3)', 'monosomy 11qter', 'chromosome 11q deletion syndrome', 'telomeric deletion 11q', 'partial 11q monosomy syndrome']",0111723,147791,2308,C0795841,,C75457,,,,,,
mondo:0007839,Aase-Smith syndrome,"['Aase-Smith syndrome type 1', 'Aase-Smith syndrome', 'Aase-Smith syndrome I', 'Aase-Smith syndrome 1', 'Joint contractures with Other abnormalities', 'hydrocephalus-cleft palate-joint contractures syndrome', 'Aase-Smith I syndrome']",,147800,916,C0220686,,,,C535332,,,10063429,
mondo:0007840,"internal carotid artery, spontaneous dissection of","['internal carotid artery, spontaneous dissection of']",,147820,,C1840073,,,,C564125,,,,
mondo:0007841,coxopodopatellar syndrome,"['ischiocoxopodopatellar syndrome with or without pulmonary arterial hypertension', 'Coxo-podo-patellar syndrome', 'congenital coxa vara, patella aplasia and tarsal synostosis', 'ischiopatellar dysplasia', 'ICPPS', 'SPS', 'small patella syndrome', 'patella aplasia, coxa vara, tarsal synostosis', 'coxopodopatellar syndrome', 'Scott-Taor syndrome', 'ischiocoxopodopatellar syndrome']",0111382,147891,1509,C1840061,"['-0.2308', '-0.1123', '-0.3457', '-0.443', '0.4514', '-0.0459', '0.1936', '1.214', '-0.774', '-0.463', '-0.0322', '-0.2004', '0.1087', '0.497', '-0.4229', '0.405', '0.104', '-0.4807', '-0.4727', '-0.1661', '-0.1813', '0.01315', '0.1063', '-0.2476', '0.1644', '0.3115', '0.1433', '0.2292', '0.5913', '-0.04126', '0.726', '-0.238', '-0.0863', '0.2491', '0.0588', '-0.3447', '-0.0627', '-0.3115', '-0.2008', '-0.0606', '0.0335', '-0.05124', '0.02838', '-0.4404', '0.1571', '-0.2455', '-0.07764', '0.1901', '0.063', '-0.2267', '0.1565', '-0.06192', '-0.476', '0.4055', '-0.5176', '-0.899', '-0.1376', '-0.3035', '-0.1769', '0.1278', '0.757', '0.1615', '-0.4695', '0.206', '-0.1631', '0.2505', '0.2593', '0.2827', '-0.2228', '0.3691', '-0.4673', '-0.09644', '0.2483', '0.3818', '0.8726', '0.6074', '0.2372', '-0.2515', '0.4219', '-0.1392', '0.1342', '-0.1846', '0.684', '0.4119', '-0.1991', '0.2125', '-0.07654', '0.2192', '0.09686', '-0.394', '-0.53', '-0.1381', '-0.4294', '0.694', '0.724', '0.1915', '0.949', '-0.568', '0.1813', '0.266']",,,C535540,,,,
mondo:0007842,"joint laxity, familial","['joint laxity, familial', 'familial joint instability syndrome', 'EDS Xi', 'Ehlers-Danlos syndrome, type 11 (formerly)', 'EDS11', 'Ehlers-Danlos syndrome type 11, formerly', 'EDS 11 (formerly)', 'EDS Xi, formerly', 'EDS11, formerly', 'articular hypermobility syndrome', 'EDS XI', 'familial joint laxity', 'Ehlers-Danlos syndrome, type Xi', 'Ehlers-Danlos syndrome, type Xi, formerly', 'Joint instability syndrome']",,147900,2295,C0268349,,,,C535884,,,,
mondo:0007843,Kabuki syndrome 1,"['Kabuki syndrome 1', 'Kabuki make-Up syndrome', 'KABUKI syndrome 1', 'Kabuki syndrome type 1', 'Niikawa-Kuroki syndrome', 'KABUK1', 'Kabuki syndrome']",,147920,,CN030661,,,,,,,,
mondo:0007844,hypogonadotropic hypogonadism 2 with or without anosmia,"['FGFR1 hypogonadotropic hypogonadism', 'Kallmann syndrome 2', 'HH2', 'hypogonadotropic hypogonadism caused by mutation in FGFR1', 'hypogonadotropic hypogonadism 2 with or without anosmia', 'KAL2']",0090083,147950,,C1563720,,,,,,E23.0,,
mondo:0007845,"Kaposi sarcoma, susceptibility to","['multicentric Castleman disease, susceptibility to', 'susceptibility to Kaposi sarcoma', 'Kaposi sarcoma, susceptibility to', 'multiple idiopathic pigmented hemangiosarcoma, susceptibility to']",,148000,160,,"['-0.02536', '0.0838', '0.05002', '-0.05316', '0.05923', '-0.118', '0.06384', '0.02687', '-0.001708', '-0.02635', '-0.03503', '0.064', '-0.03763', '0.03125', '-0.05698', '-0.0637', '0.00931', '-0.07043', '-0.02582', '-0.1522', '0.01788', '-0.0943', '0.0954', '-0.05844', '-0.01857', '0.002369', '-0.02193', '-0.00909', '-0.0683', '-0.0667', '0.0955', '-0.03635', '0.11584', '-0.02432', '0.04688', '0.00843', '-0.04404', '0.002798', '-0.03183', '-0.0758', '0.0356', '-0.0672', '0.0364', '-0.06604', '0.003607', '-0.0762', '-0.01726', '0.07574', '0.02039', '0.01726', '-0.04117', '-0.02853', '0.06036', '0.036', '-0.0668', '-0.001385', '0.03568', '-0.04825', '-0.06274', '0.00769', '0.0646', '0.05984', '-0.0297', '0.05234', '0.02892', '0.03323', '0.07764', '0.11597', '-0.0839', '0.2007', '-0.06287', '0.0172', '0.02072', '-0.04446', '0.05505', '0.051', '-0.06805', '0.0085', '-0.02007', '-0.09515', '-0.0481', '-0.004047', '-0.05945', '0.126', '-0.0654', '-0.03046', '0.0842', '0.0493', '0.1003', '-0.01895', '0.02841', '0.04465', '-0.04938', '0.00416', '0.169', '0.0665', '0.1049', '-0.0874', '-0.079', '-0.02557']",,,,,,,
mondo:0007846,KBG syndrome,"['macrodontia, intellectual disability, characteristic facies, short stature, and skeletal anomalies', 'short stature, characteristic facies, macrodontia, intellectual disability, and skeletal anomalies', 'short stature, characteristic facies, macrodontia, mental retardation, and skeletal anomalies', 'short stature-facial and skeletal anomalies-intellectual disability-macrodontia syndrome', 'KBGS', 'KBG syndrome', 'macrodontia, mental retardation, characteristic facies, short stature, and skeletal anomalies']",14780,148050,2332,C0220687,"['0.3071', '0.0774', '0.508', '-0.3438', '0.1699', '0.164', '0.4756', '1.612', '-0.966', '-0.0841', '-0.669', '-0.4822', '0.352', '0.4165', '-0.11194', '0.3315', '0.1542', '-0.3044', '-1.002', '-0.4736', '0.2861', '-0.03418', '0.3748', '-0.3225', '0.4854', '-0.2367', '-0.2527', '-0.1349', '0.373', '-0.325', '0.5186', '-0.1124', '-0.10956', '-0.2747', '0.4927', '0.1752', '-0.3684', '-0.938', '-0.4163', '-0.3806', '0.1315', '-0.0428', '-0.002508', '-0.1989', '0.3726', '-0.2854', '-0.1388', '0.2537', '-0.10187', '0.2499', '-0.2277', '0.603', '-0.804', '0.1746', '-0.4954', '-0.308', '0.08844', '-0.4983', '0.04614', '-0.07825', '0.588', '0.1614', '-0.0601', '0.1326', '-0.00495', '0.1927', '-0.0444', '0.08514', '0.1174', '0.1874', '-0.1187', '0.1676', '-0.381', '-0.0697', '0.26', '-0.235', '0.4292', '-0.3784', '-0.3452', '-0.05255', '0.6084', '-0.531', '-0.5737', '0.591', '0.04486', '0.1393', '-0.2351', '0.1539', '0.39', '0.01598', '-0.1257', '0.2654', '-0.3613', '0.0712', '0.6567', '0.1896', '0.2617', '-0.9136', '0.9873', '0.01056']",,,C537015,759.89,,,
mondo:0007847,keloid formation,['keloid formation'],,148100,,,,,,,,,,
mondo:0007848,autosomal dominant keratitis,"['dominantly inherited keratitis', 'keratitis, autosomal dominant', 'hereditary keratitis', 'keratitis, hereditary']",0111383,148190,2334,CN068649,"['0.1318', '-0.07324', '-0.204', '0.609', '-0.2249', '-0.664', '-0.2446', '0.2042', '-0.3035', '-0.431', '0.2312', '0.253', '-0.582', '0.8037', '-0.8354', '-0.1915', '0.1796', '0.3796', '-0.3289', '-0.5513', '-0.4973', '0.4316', '-0.3655', '0.03613', '-0.6123', '-0.4314', '-0.9766', '0.686', '0.02423', '-0.435', '0.1222', '0.02716', '0.3284', '0.1365', '0.3525', '0.438', '0.4104', '-0.874', '0.877', '-0.528', '0.5547', '0.2024', '-0.1881', '-0.53', '-0.1877', '0.1586', '0.08765', '-0.3254', '0.03473', '-0.07477', '-0.1316', '-0.4485', '0.6924', '-0.4019', '0.09717', '-0.1732', '0.2625', '-0.2493', '-0.6436', '-1.074', '-0.05496', '-0.1517', '-0.2347', '0.3232', '-0.06354', '-0.25', '0.5127', '0.006195', '-0.01416', '0.7114', '0.03555', '0.10645', '0.3655', '-0.9727', '0.7275', '0.3904', '0.2358', '0.632', '0.4216', '0.5576', '-0.3154', '-0.3608', '-0.1538', '0.653', '-0.2379', '-0.219', '0.5464', '0.7637', '0.02097', '0.7793', '-0.0576', '0.1305', '-0.651', '0.258', '0.481', '0.0398', '0.3882', '-1.033', '-0.4346', '-0.3806']",,,C537022,,,,
mondo:0007849,keratitis fugax hereditaria,"['keratoendotheliitis fugax hereditaria', 'KEFH', 'KERATOENDOTHELIITIS fugax hereditaria', 'keratoendothelitis fugax hereditaria', 'keratitis fugax hereditaria', 'Keratoendotheliitis fugax hereditaria']",,148200,,C1835697,"['-0.01953', '0.03082', '0.00962', '-0.01917', '-0.001591', '-0.02812', '0.002716', '0.01895', '0.00086', '-0.01402', '-0.02066', '-0.0146', '-0.01002', '0.01309', '-0.01813', '-0.004227', '0.01293', '-0.01604', '-0.01712', '-0.05536', '-0.01698', '-0.01559', '0.01142', '-0.01484', '0.00586', '-0.01534', '4.977e-05', '0.003119', '0.00291', '-0.02145', '0.01327', '-0.01817', '0.02109', '0.006092', '0.001162', '-0.001075', '-0.00414', '-0.01938', '-0.000499', '-0.02652', '0.01959', '-0.01773', '0.0224', '-0.007763', '-0.00992', '-0.02875', '-0.001062', '0.01714', '0.002888', '0.00901', '0.004272', '0.005688', '0.02872', '0.01688', '-0.02599', '-0.00439', '0.03598', '-0.02623', '-0.05405', '-0.001687', '0.01656', '0.0162', '-0.0048', '0.005886', '0.00778', '0.00754', '0.03162', '0.02219', '-0.02164', '0.0381', '-0.01582', '-0.01066', '0.002048', '-0.03004', '0.002945', '0.017', '0.013725', '-0.01044', '-0.005566', '-0.01639', '-0.001646', '0.005356', '-0.01762', '0.02795', '0.0008388', '0.002254', '0.006584', '0.04135', '0.02396', '0.00351', '0.003382', '0.01683', '0.0082', '0.012924', '0.04135', '0.01007', '0.0349', '-0.03925', '-0.00972', '0.01388']",,,C563650,,,,
mondo:0007850,autosomal dominant keratitis-ichthyosis-hearing loss syndrome,"['keratitis-ichthyosis-deafness syndrome, autosomal dominant', 'autosomal dominant KID syndrome', 'autosomal dominant keratitis-ichthyosis-deafness syndrome', 'KID syndrome, autosomal dominant', 'keratitis-ichthyosis -deafness syndrome']",0060871,148210,,,,,,,,,,
mondo:0007851,keratoconus 1,"['keratoconus type 1', 'KTCN1', 'VSX1 keratoconus (disease)', 'keratoconus 1']",,148300,,C1835677,,,,C563649,,,,
mondo:0007852,palmoplantar keratoderma-deafness syndrome,"['keratoderma, palmoplantar, with deafness', 'focal palmoplantar keratoderma with sensorineural deafness (subtype)', 'palmoplantar keratoderma and sensorineural deafness', 'palmoplantar keratoderma-hearing loss syndrome', 'keratoderma palmoplantar deafness', 'keratoderma palmoplantar, with deafness', 'palmoplantar hyperkeratosis-hearing loss syndrome', 'diffuse palmoplantar keratoderma with deafness (subtype)', 'hereditary palmoplantar keratoderma with deafness (subtype)', 'PPK-deafness syndrome', 'palmoplantar hyperkeratosis-deafness syndrome']",0111505,148350,2202,C1835672,"['-0.2444', '0.2705', '-0.0481', '0.1032', '0.3372', '-0.6816', '-0.1971', '0.4426', '-0.0387', '-0.1735', '-0.1335', '-0.1037', '-0.3618', '-0.3506', '0.335', '0.4329', '0.2515', '-0.651', '0.0885', '-0.785', '-0.0362', '-0.2673', '0.3792', '0.1575', '0.4', '0.494', '-0.1948', '0.579', '-0.1027', '0.1056', '0.515', '-0.0959', '0.0569', '0.269', '-0.107', '-0.2274', '0.0459', '-0.05167', '0.1478', '-0.2656', '-0.2612', '-0.0847', '0.1595', '-0.1943', '0.003029', '-0.3652', '-0.399', '0.3394', '-0.1186', '-0.2764', '0.1371', '-0.02998', '-0.1382', '0.044', '0.193', '-0.645', '0.635', '-0.003277', '-0.4353', '-0.2659', '-0.1903', '-0.0673', '-0.0477', '-0.182', '-0.1382', '0.4954', '0.1288', '0.53', '-0.4014', '0.575', '-0.657', '-0.06033', '0.539', '0.2834', '0.497', '-0.12024', '0.1176', '0.277', '-0.002377', '-0.2585', '0.488', '0.4138', '0.06207', '0.165', '0.3542', '-0.4028', '-0.0402', '0.8105', '0.05728', '0.4973', '0.173', '0.4546', '0.1862', '0.3098', '0.6426', '-0.2705', '0.326', '-0.7285', '0.3848', '-0.07556']",,,C536152,,,,
mondo:0007853,palmoplantar keratoderma-hereditary motor and sensory neuropathy syndrome,"['keratoderma, palmoplantar, with nail dystrophy and hereditary motor-sensory neuropathy', 'Charcot-Marie-Tooth disease with palmoplantar keratoderma and nail dystrophy', 'axonal neuropathy with palmoplantar keratoderma']",,148360,538574,,,,,C536153,,,,
mondo:0007854,keratolytic winter erythema,"['keratolytic WINTER erythema', 'keratolytic winter erythema', 'Oudtshoorn skin disease', 'Erythrokeratolysis hiemalis', 'Erythrokeratolysis hiemalis ichthyosis', 'Oudtshoorn disease', 'Oudtshoorn skin', 'KWE']",,148370,50943,C0406756,"['-0.1274', '0.3047', '-0.2452', '-0.2837', '0.02058', '-0.544', '-0.0334', '-0.1414', '-0.11475', '-0.0926', '-0.1501', '0.3096', '-0.2153', '-0.1965', '-0.11', '0.3083', '0.3574', '-0.4805', '-0.05087', '-0.537', '-0.1456', '-0.2355', '0.2961', '0.05737', '0.1842', '0.205', '-0.0992', '0.273', '-0.183', '-0.3281', '-0.0007844', '-0.1617', '-0.1998', '0.0817', '0.11084', '0.07904', '-0.0973', '-0.02222', '0.2029', '-0.2488', '-0.267', '-0.4421', '0.1509', '0.01671', '0.12354', '-0.2499', '-0.4412', '0.3694', '0.1313', '0.1064', '-0.416', '-0.1678', '0.1471', '0.001015', '-0.2725', '-0.1898', '0.546', '-0.03723', '-0.545', '-0.4038', '0.1694', '0.1433', '-0.4827', '0.05615', '0.04874', '0.2285', '0.3904', '0.4626', '0.2203', '0.4915', '-0.4343', '-0.11316', '0.1348', '-0.12115', '0.1672', '0.0695', '0.0954', '0.05185', '0.2184', '-0.357', '-0.0678', '-0.04114', '0.4656', '0.1566', '0.003595', '0.1371', '-0.2522', '0.5737', '0.0912', '0.3464', '0.2421', '0.1356', '-0.03026', '0.3394', '0.1958', '0.1355', '0.4739', '-0.563', '-0.233', '0.1323']",,,C536155,695.89,,,
mondo:0007855,"keratosis, familial actinic","['keratosis, familial actinic']",,148390,,C2675099,,,,C567190,,,,
mondo:0007856,palmoplantar keratoderma-esophageal carcinoma syndrome,"['tylosis-oesophageal carcinoma syndrome', 'Howell-Evans syndrome', 'palmoplantar keratoderma-esophageal carcinoma syndrome', 'keratosis palmoplantaris with esophageal cancer', 'palmoplantar keratoderma with esophageal cancer', 'tylosis - oesophageal carcinoma', 'tylosis with esophageal cancer', 'Bennion-Patterson syndrome', 'keratosis palmoplantaris-esophageal carcinoma syndrome', 'keratosis palmaris Et plantaris with esophageal cancer', 'howel-Evans syndrome', 'keratosis palmaris et plantaris with esophageal cancer', 'palmoplantar hyperkeratosis-esophageal carcinoma syndrome', 'Toc']",0111506,148500,2198,,"['0.818', '0.509', '-0.3608', '-0.2423', '0.3042', '-0.44', '-0.09686', '0.27', '-0.3022', '-0.1669', '0.10223', '0.254', '-0.4844', '-0.4297', '-0.3608', '-0.2108', '0.4238', '-0.628', '0.09357', '-0.7603', '-0.3499', '-0.3928', '0.1621', '-0.1434', '0.1876', '0.3647', '-0.07086', '0.4182', '-0.1748', '-0.289', '0.402', '-0.06537', '0.2798', '-0.318', '0.006718', '0.259', '-0.1763', '-0.05267', '0.2915', '-0.04498', '-0.2927', '-0.2383', '0.2842', '-0.002974', '-0.1565', '0.009026', '-0.475', '0.09015', '0.5034', '0.11536', '-0.01797', '0.168', '0.228', '-0.085', '-0.1587', '0.0932', '0.4302', '0.1283', '-0.634', '-0.4907', '0.2874', '0.309', '0.1664', '-0.479', '0.3013', '0.4976', '0.5166', '0.2153', '-0.2014', '0.524', '-0.2284', '-0.0816', '0.1055', '0.1537', '0.542', '-0.2915', '-0.1293', '0.1859', '0.0348', '-0.4812', '-0.3533', '0.2576', '0.272', '-0.4026', '0.1649', '-0.3962', '-0.2576', '0.6445', '0.3313', '0.392', '-0.3115', '0.2515', '0.1663', '0.02525', '0.1974', '0.1343', '0.5728', '-0.4993', '-0.02797', '-0.3145']",,,C536164,,,,
mondo:0007857,keratosis palmaris et plantaris-clinodactyly syndrome,"['keratosis palmaris ET plantaris with clinodactyly', 'palmoplantar keratoderma-clinodactyly syndrome']",,148520,86919,C1835663,,,,C563646,,,,
mondo:0007858,"palmoplantar keratoderma, punctate type 1A","['keratodermia palmoplantaris papulosa, Buschke-Fischer-Brauer type', 'keratosis palmoplantaris papulosa', 'punctate palmoplantar keratoderma type 1A', 'palmoplantar keratoderma, punctate type 1', 'PPKP1A', 'palmoplantar keratoderma, punctate type IA', 'Kppp1', 'punctate palmoplantar keratoderma caused by mutation in AAGAB', 'keratoderma, palmoplantar, punctate type IA', 'AAGAB punctate palmoplantar keratoderma']",0080214,148600,,,,,,,,,,
mondo:0007859,"palmoplantar keratoderma i, striate, focal, or diffuse","['keratoderma, palmoplantar striate form 1', 'PPKS1', 'SPPK1', 'keratosis palmoplantaris striata 1', 'palmoplantar keratoderma i, striate, focal, or diffuse', 'striate palmoplantar keratoderma 1', 'keratoderma, palmoplantar, striate form 1', 'keratosis palmoplantaris striata i, AD', 'palmoplantar keratoderma I, striate, focal, or diffuse']",0081108,148700,370002,,"['-0.008194', '0.2456', '0.1002', '-0.08765', '0.09796', '-0.4731', '-0.0644', '0.1137', '-0.2842', '0.05972', '-0.2534', '0.0778', '-0.1526', '-0.01657', '-0.1967', '0.1533', '0.3347', '-0.3784', '0.09436', '-0.761', '-0.2512', '0.06232', '0.53', '0.1526', '0.004726', '0.2461', '-0.02599', '0.2351', '-0.0637', '-0.004803', '0.10034', '-0.3245', '0.0981', '0.2213', '0.2527', '-0.0842', '-0.1912', '-0.10516', '0.12054', '-0.329', '-0.1183', '-0.501', '-0.012665', '0.2079', '0.1912', '-0.1829', '-0.1197', '0.3584', '0.09076', '0.009224', '-0.3618', '0.11145', '0.3613', '0.254', '-0.2886', '-0.2366', '0.3552', '-0.0186', '-0.3943', '-0.4656', '0.1804', '-0.0385', '-0.4407', '-0.1388', '-0.05637', '0.2034', '0.2515', '0.471', '0.157', '0.3823', '-0.3806', '-0.2048', '0.1842', '-0.05527', '0.00622', '0.06158', '0.046', '0.05634', '-0.1633', '-0.307', '-0.2732', '0.1019', '0.1832', '0.1117', '0.2001', '-0.1498', '-0.2886', '0.4678', '0.1844', '0.2168', '0.139', '0.2472', '0.1744', '0.266', '0.191', '0.04175', '0.414', '-0.2566', '0.1747', '0.2878']",,,C536162,,,,
mondo:0007860,focal palmoplantar and gingival keratoderma,"['focal palmoplantar and oral mucosa hyperkeratosis', 'keratosis focal palmoplantar gingival', 'focal palmoplantar and gingival hyperkeratosis', 'focal palmoplantar and gingival hyperkeratosis syndrome', 'keratosis, focal palmoplantar and gingival']",,148730,2200,C1835650,,,,C536157,,,,
mondo:0007861,isolated cloverleaf skull syndrome,"['Kleeblattschaedel syndrome', 'cloverleaf skull', 'Kleeblattschaedel-deformity syndrome', 'cloverleaf skull syndrome', 'Kleeblattschaedel deformity syndrome', 'Kleeblattschadel', 'KLEEBLATTSCHAEDEL', 'isolated cloverleaf skull syndrome']",,148800,2343,CN201565,"['-0.1849', '0.2644', '0.1172', '-0.4998', '-0.01884', '0.001451', '0.1031', '-0.1554', '-0.767', '0.097', '-0.3677', '-0.2434', '0.287', '-0.2219', '-0.3882', '-0.1396', '0.07623', '-0.201', '0.0771', '-0.7456', '0.1494', '0.3733', '0.603', '-0.09955', '0.2932', '0.2292', '0.11224', '0.3853', '0.574', '0.1338', '0.08966', '-0.10986', '0.8857', '0.05048', '0.07587', '-0.06256', '-0.3027', '-0.2267', '-0.313', '-0.878', '0.2725', '-0.405', '0.3125', '-0.6543', '0.094', '-0.1975', '0.05603', '0.3574', '0.073', '-0.0727', '0.3083', '-0.252', '-0.07776', '0.05255', '-0.5195', '0.1279', '-0.1659', '0.2021', '-0.2625', '0.1799', '-0.0462', '-0.2622', '-0.06525', '-0.02007', '-0.326', '0.02878', '0.2194', '0.4844', '-0.6016', '0.198', '-0.2998', '0.4568', '0.621', '-0.3586', '-0.2747', '0.612', '0.5996', '-0.1727', '-0.4023', '-0.782', '-0.1353', '-0.09973', '-0.3438', '0.729', '0.2534', '0.12225', '0.06018', '0.1174', '0.2573', '-0.11847', '-0.2155', '0.4832', '0.4958', '0.1566', '0.532', '-0.1311', '0.6265', '-0.09155', '0.478', '0.178']",,,C536884,,,,
mondo:0007862,Waardenburg syndrome type 3,"['Waardenburg syndrome type III', 'Klein-Waardenburg syndrome', 'Waardenburg syndrome, type 3', 'Waardenburg syndrome with upper limb anomalies', 'White forelock (poliosis) syndrome with multiple congenital malformations', 'Waardenburg syndrome with limb anomalies', 'WS3']",0110949,148820,896,,"['0.1874', '-0.0814', '0.36', '-0.02298', '0.7964', '-0.2472', '0.292', '0.1553', '-0.5474', '-0.0446', '-0.2186', '-0.132', '-0.3208', '0.3608', '-0.53', '-0.736', '0.3547', '-0.1254', '-0.3333', '-0.4297', '-0.1464', '-0.1376', '0.3796', '-0.1987', '-0.3267', '0.1647', '-0.214', '0.1637', '0.1589', '-0.4182', '0.1743', '0.11163', '-0.1835', '-0.2524', '-0.1995', '0.01675', '0.163', '-0.2783', '-0.373', '-0.2251', '0.801', '-0.8887', '0.4663', '-0.1103', '0.0765', '-0.7583', '0.2742', '0.2285', '0.356', '0.0529', '-0.2285', '-0.718', '0.1564', '-0.391', '-0.591', '-0.4924', '-0.4795', '0.0631', '-0.513', '-0.649', '-0.7007', '-0.5415', '-0.01347', '0.0376', '-0.4126', '-0.0981', '-0.1206', '0.2783', '-0.342', '0.1525', '-0.4016', '-0.04153', '-0.2632', '-0.03072', '0.2441', '0.02193', '0.0477', '-0.5166', '-0.3774', '-0.642', '0.1989', '-0.7144', '0.1844', '0.8545', '-0.5625', '-0.2668', '0.1769', '0.5615', '0.1854', '-0.02774', '0.4263', '0.638', '0.2861', '-0.0343', '0.4165', '-0.209', '0.2944', '-0.311', '0.201', '0.31']",,,,,E70.3,,
mondo:0007863,Kleine-Levin syndrome,"['familial hibernation syndrome', 'Kleine Levin syndrome', 'familial Kleine-Levin syndrome', 'Kleine-LEVIN hibernation syndrome', 'Kleine-Levin syndrome']",0060165,148840,33543,C0206085,,C84800,1001354,D017593,,,10053712,
mondo:0007864,angioosteohypertrophic syndrome,"['Klippel-Trenaunay-Weber syndrome', 'angio-osteohypertrophy syndrome', 'Ktw syndrome', 'Weber-Klippel-Trenaunay', 'angioosteohypertrophy syndrome', 'Klippel-Trenaunay syndrome', 'KTS', 'Klippel-Trénaunay syndrome', 'Klippel-Trenaunay-Weber syndrome, Isolated cases', 'haemangiectatic hypertrophy', 'Klippel Trenaunay syndrome']",2926,149000,90308,CN201567,"['-0.0715', '0.0811', '0.0317', '-0.0342', '0.05826', '-0.12463', '0.01157', '0.1335', '-0.1395', '-0.05173', '-0.0389', '6.06e-05', '0.002277', '0.05383', '-0.10486', '-0.04337', '-0.0006804', '-0.05368', '-0.05264', '-0.2277', '-0.01362', '-0.0354', '0.1615', '-0.05212', '0.0391', '-0.005154', '-0.0623', '-0.03125', '0.06445', '-0.07666', '0.10455', '-0.05392', '0.1088', '0.0589', '0.02469', '-0.0577', '-0.06854', '-0.01326', '0.006237', '-0.1772', '0.0909', '-0.1436', '0.02307', '-0.0556', '0.0513', '-0.0874', '-0.04495', '0.11975', '0.0724', '0.0126', '-0.0399', '-0.011505', '0.083', '0.03119', '-0.1047', '-0.06616', '0.0792', '-0.03403', '-0.1571', '-0.02414', '0.11456', '0.06854', '-0.0775', '-0.004898', '-0.01733', '-0.01384', '0.1351', '0.1415', '-0.11237', '0.1617', '-0.1184', '0.02568', '0.05734', '-0.0642', '0.03323', '0.05585', '0.02498', '0.01382', '-0.09393', '-0.0737', '-0.0477', '-0.0157', '-0.0149', '0.10626', '-0.04523', '0.01622', '0.02008', '0.1035', '0.1522', '-0.02281', '0.02823', '0.1237', '0.0277', '0.05963', '0.2045', '0.02095', '0.1175', '-0.1976', '0.02496', '0.08435']",C84801,0007334,D007715,,,10051452,
mondo:0007865,knuckle pads,['knuckle pads'],,149100,,C0264000,,,,,728.79,M72.1,,
mondo:0007866,Bart-Pumphrey syndrome,"['Bart-Pumphrey syndrome', 'knuckle pads-leukonychia-sensorineural deafness-palmoplantar hyperkeratosis syndrome', 'knuckle pads, leukonychia, and sensorineural deafness', 'knuckle pads, leuconychia and sensorineural deafness', 'knuckle pads-leukonychia-sensorineural deafness-palmoplantar keratoderma syndrome']",0050658,149200,2698,,"['-0.279', '0.1265', '0.1613', '-0.1337', '0.2286', '-0.3918', '-0.0736', '0.1658', '-0.2268', '-0.03876', '-0.178', '0.10657', '0.002567', '-0.1138', '-0.10394', '-0.0304', '0.2457', '-0.149', '0.1019', '-0.594', '0.0008454', '0.05368', '0.2152', '0.0824', '0.2317', '0.2499', '-0.1755', '0.1071', '0.001894', '-0.1388', '0.1359', '-0.003014', '0.1333', '0.178', '0.1043', '-0.323', '-0.173', '-0.1711', '-0.068', '-0.307', '-0.01325', '-0.1858', '-0.117', '0.010574', '0.05637', '-0.1154', '-0.2048', '0.2524', '0.1729', '-0.11786', '-0.2036', '-0.0604', '0.127', '-0.0637', '-0.2915', '-0.1787', '0.3179', '-0.04803', '-0.356', '0.0142', '0.1685', '-0.0567', '-0.2119', '0.03317', '-0.1192', '-0.0879', '0.0935', '0.4177', '-0.08026', '0.301', '-0.455', '-0.10425', '0.1628', '-0.03757', '0.1036', '-0.112', '0.1268', '0.01639', '-0.12494', '-0.1523', '-0.00338', '0.04816', '0.06033', '0.268', '0.0957', '-0.00811', '-0.1489', '0.484', '0.1256', '0.1785', '0.2646', '0.421', '0.2336', '0.1111', '0.2827', '-0.1044', '0.5005', '-0.457', '0.1667', '0.1037']",,,C537210,759.89,,,
mondo:0007867,nonsyndromic congenital nail disorder 2,"['congenital koilonychia', 'Koilonychia, hereditary', 'nail disorder, nonsyndromic congenital, 2', 'spoon nails', 'Koilonychia with leukonychia', 'nonsyndromic congenital nail disorder type 2', 'familial koilonychia', 'hereditary koilonychia', 'NDNC2']",0080080,149300,,,,,,C537260,703.8,,,
mondo:0007868,hyperekplexia 1,"['startle disease, familial', 'Stiff-baby syndrome', 'Sthe', 'exaggerated startle reaction', 'startle reaction, exaggerated', 'hyperekplexia, hereditary type 1', 'hyperekplexia type 1', 'Stiff-Man syndrome, congenital', 'hyperekplexia, hereditary 1', 'HKPX1', 'Stiff-Person syndrome, congenital', 'hyperekplexia 1', 'Kok disease']",0060696,149400,,,,,,,,,,
mondo:0007869,Kyrle disease,"['hyperkeratosis follicularis et parafollicularis in cutem penetrans', 'Kyrle disease', 'Kyrle^s disease']",,149500,,C0263382,,,,C538130,,,,
mondo:0007870,"labia minora, incomplete adhesion of","['labia minora, incomplete adhesion of']",,149600,,,,,,,,,,
mondo:0007871,familial congenital nasolacrimal duct obstruction,"['lacrimal duct defect', 'LCDD', 'nasolacrimal duct obstruction', 'lacrimal puncta, absence of']",,149700,451612,,,,,C566703,,,,
mondo:0007872,LADD syndrome,"['lacrimoauriculodentodigital syndrome', 'LACRIMOAURICULODENTODIGITAL syndrome', 'Levy-Hollister syndrome', 'LADD syndrome', 'lard syndrome', 'Lacrimo-auriculo-dento-digital syndrome', 'Levy Hollister syndrome', 'LADD', 'Lacrimoauriculoradiodental syndrome', 'Lacrimoauriculodento-digital syndrome']",0050331,,2363,C0265269,"['0.0153', '-0.131', '0.4668', '-0.357', '-0.10986', '-0.02238', '0.1054', '0.1555', '-0.1234', '-0.4138', '-0.2825', '-0.393', '-0.6196', '0.3225', '-0.3142', '-0.2467', '0.1296', '-0.3225', '-0.282', '-0.3545', '0.2542', '-0.1759', '0.1519', '-0.39', '0.7163', '0.0825', '-0.6016', '0.131', '0.509', '-0.5684', '0.2954', '0.04648', '-0.205', '0.3423', '0.3857', '-0.4312', '-0.07654', '-0.1583', '-0.4883', '-0.1929', '0.0391', '0.1438', '0.1262', '-0.4841', '0.1433', '-0.4648', '0.0682', '0.3723', '-0.0269', '0.1539', '-0.3455', '0.1919', '0.159', '0.01663', '-0.7485', '-0.3748', '0.05963', '-0.1068', '-0.3464', '-0.3223', '0.3518', '0.0525', '-0.3376', '-0.218', '-0.299', '-0.1885', '0.4158', '0.7656', '-0.3152', '0.131', '-0.3906', '0.0455', '0.5073', '-0.5034', '0.1968', '0.02051', '0.3162', '-0.1081', '-0.1356', '-0.08295', '-0.1255', '-0.1631', '0.085', '0.702', '-0.0678', '-0.2974', '-0.2542', '0.1208', '-0.1418', '-0.0676', '-0.1709', '0.7324', '0.585', '0.1443', '0.6924', '-0.3894', '0.4763', '-0.5854', '0.463', '0.3975']",,,C538132,759.89,,,
mondo:0007873,"lactic acidosis, chronic adult form","['lactic acidosis, chronic adult form']",,150170,,C1835591,,,,C563640,,,,
mondo:0007874,trichorhinophalangeal syndrome type II,"['TRPS 2', 'chromosome 8Q24.1 deletion syndrome', 'trichorhinophalangeal syndrome, type 2', 'deletion 8q24.1', 'TRPS2', 'trichorhinophalangeal dysplasia type II', 'Giedion-Langer syndrome', 'trichorhinophalangeal syndrome type 2', 'Langer-Giedion syndrome', 'Langer Giedion syndrome', 'trichorhinophalangeal syndrome, type II', 'monosomy 8q24.1']",4998,150230,502,C0023003,"['-0.0525', '-0.3037', '0.2542', '-0.28', '0.275', '-0.4558', '0.2166', '0.4763', '-0.831', '-0.2925', '0.1029', '0.6777', '0.0895', '-0.2001', '0.05396', '0.126', '0.366', '0.2703', '-0.4434', '-0.5127', '0.1672', '0.3271', '0.3289', '-0.58', '0.4465', '0.2014', '-0.4663', '-0.0998', '0.2646', '0.07275', '0.3933', '-0.2585', '-0.04446', '0.03558', '0.185', '-0.0305', '-0.1236', '-0.511', '-0.08636', '0.362', '0.4868', '-0.3037', '-0.08325', '-0.2563', '0.2062', '-0.7573', '-0.1672', '0.5234', '0.107', '-0.3896', '-0.5005', '0.4128', '-0.1092', '0.11035', '-0.37', '-0.2283', '-0.006516', '0.2793', '0.0754', '0.01532', '-0.0159', '0.1599', '-0.532', '-0.03275', '0.104', '0.0649', '0.2349', '0.366', '-0.706', '0.473', '-0.4111', '-0.0525', '0.2905', '-0.1427', '0.03223', '-0.0786', '0.04364', '0.1597', '-0.1443', '0.1733', '-0.1307', '-0.3088', '0.3804', '0.6426', '-0.205', '-0.4343', '-0.3247', '0.4192', '0.189', '0.4143', '-0.0735', '0.501', '0.3281', '0.1779', '0.3484', '0.3271', '0.758', '-0.781', '0.6353', '0.09674']",C75118,,D015826,759.89,,10050638,
mondo:0007875,Larsen syndrome,"['autosomal dominant Larsen syndrome', 'Larsen syndrome', 'LRS', 'dominant Larsen syndrome']",14764,150250,503,C0175778,"['0.398', '-0.1545', '-0.0092', '-0.11304', '0.7246', '-0.5225', '0.1376', '1.132', '-0.9277', '-0.7373', '0.0882', '0.2079', '0.387', '0.674', '-0.321', '0.263', '0.124', '-0.523', '-0.3262', '-0.657', '-0.2363', '0.011154', '0.7417', '0.1323', '-0.0647', '0.3926', '-0.1862', '-0.0492', '0.5957', '-0.2186', '0.1326', '-0.2142', '-0.1278', '0.08746', '0.07874', '-0.2441', '-0.1316', '-0.6523', '0.03546', '-0.001854', '-0.3289', '0.1383', '0.2137', '-0.092', '0.1681', '-0.1849', '-0.387', '0.2129', '-0.1888', '-0.1741', '-0.2461', '-0.2052', '0.1444', '-0.2932', '-0.11115', '-0.6055', '0.04916', '0.1027', '0.2656', '-0.09607', '0.3967', '0.1461', '-0.634', '0.389', '-0.326', '0.3486', '0.0777', '0.004845', '0.07776', '0.3877', '-0.1893', '0.03925', '-0.256', '-0.542', '-0.1855', '0.2444', '-0.004772', '-0.2798', '-0.3584', '-0.5044', '-0.1057', '-0.09064', '0.02533', '1.348', '-0.1494', '0.5728', '0.4348', '0.1682', '0.06616', '-0.04822', '-0.1284', '0.09204', '0.2247', '0.1375', '0.677', '-0.2367', '0.603', '-0.3071', '0.363', '0.1453']",,,C580241,759.89,,,
mondo:0007876,laryngeal abductor paralysis,"['familial vocal cord dysfunction', 'Labd', 'Gerhardt syndrome', 'laryngeal abductor paralysis', 'vocal cord dysfunction, familial', 'vocal cord dysfunction familial']",,150260,2808,CN202762,,,,,748.3,,,
mondo:0007877,laryngeal adductor paralysis,"['laryngeal adductor paralysis', 'LAP', 'vocal cord dysfunction, adductor type']",,150270,,,,,,C562861,,,,
mondo:0007878,congenital laryngomalacia,"['laryngomalacia', 'congenital laryngeal stridor', 'laryngomalacia congenital']",0080833,150280,2373,,,C98971,,D055092,748.3,Q31.5,10060786,
mondo:0007879,larynx atresia,"['laryngeal atresia', 'congenital partial atresia of the larynx', 'congenital atresia of the larynx', 'larynx, congenital partial atresia OF', 'congenital atresia of larynx']",,150300,1202,C0265756,,C98972,,C563637,748.3,,,
mondo:0007880,congenital laryngeal web,"['subglottic bar, congenital heart disease and low stature', 'subglottic Bar', 'glottic web, congenital anterior', 'gay Feinmesser Cohen syndrome', 'laryngeal web, congenital heart disease and low stature', 'laryngeal web, familial', 'subglottic web', 'Laryngeal web']",,150360,2374,,,C98970,,C563636,,,10023871,
mondo:0007881,"tooth agenesis, selective, 4","['tooth agenesis caused by mutation in WNT10A', 'lateral incisors, absence of', 'STHAG4', 'WNT10A tooth agenesis', 'tooth agenesis, selective, 4, with or without ectodermal dysplasia', 'lateral incisors, pegged or missing', 'tooth agenesis, selective, type 4', 'tooth agenesis, selective, 4', 'succedaneous teeth, agenesis of']",,150400,,,,,,C563634,,,,
mondo:0007882,lattice degeneration of retina leading to retinal detachment,['lattice degeneration of retina leading to retinal detachment'],,150500,,C1835491,,,,C563633,,,,
mondo:0007883,"periodic fever, immunodeficiency, and thrombocytopenia syndrome",['lazy leukocyte syndrome'],,150550,,C0272174,,,,C562721,288.09,,,
mondo:0007884,"leg ulcers, familial, of juvenile onset","['leg ulcers, familial, of juvenile onset']",,150590,,C1835489,,,,C563632,,,,
mondo:0007885,Legg-Calve-Perthes disease,"['LCPD', 'Lcp', 'pseudocoxalgia', 'osteochondritis of the capital femoral epiphysis', 'osteochondrosis of Legg-Calve-Perthes', 'Legg-Calve-Perthes disease', 'Calve - Perthes^ disease', 'coxa plana', 'Perthes disease', 'aseptic necrosis of the capital femoral epiphysis', 'Legg-Calvé-Perthes disease', 'Legg-Perthes disease', 'Legg-Calve-Perthes syndrome', 'juvenile osteochondrosis of hip and/or pelvis', 'Legg-Calve-Perthes symptom', 'Legg-CALVE-Perthes disease', 'juvenile osteochond-hip/pelvis', 'juvenile osteochondrosis of hip and pelvis', 'Pseudocoxalgia', 'Osteochondrosis of the capital femoral epiphysis', 'Perthe^s disease', 'osteochondritis deformans']",14415,150600,2380,C0023234,"['0.2915', '-0.1838', '-0.796', '0.2395', '0.2715', '-0.723', '0.607', '1.151', '-1.129', '-1.006', '0.2277', '-0.02861', '-0.09717', '0.8115', '-0.2073', '0.3467', '0.3674', '-0.03677', '0.12244', '-0.04205', '-0.547', '-0.2507', '0.2847', '-0.2573', '0.1921', '0.509', '0.1676', '0.4763', '-0.03366', '0.1553', '-0.09467', '-0.1669', '0.012665', '0.4355', '-0.311', '0.257', '-0.3013', '-0.801', '0.02168', '-0.8193', '0.2253', '-0.2338', '-0.3425', '-0.06494', '0.299', '0.3418', '-0.525', '-0.10425', '0.09424', '-0.1163', '0.0932', '-0.1348', '0.3926', '0.1696', '0.1863', '-0.3472', '-0.451', '-0.2952', '-0.571', '0.02336', '0.4993', '0.313', '0.0463', '0.7256', '-0.1997', '0.2311', '0.7207', '0.2786', '-0.2725', '-0.0682', '0.2086', '-0.014694', '-0.001174', '-0.277', '0.444', '0.3223', '-0.67', '0.895', '0.1366', '-0.902', '-0.3716', '-0.3984', '-0.544', '-0.1669', '-0.3738', '0.385', '0.2866', '0.1649', '0.1821', '-0.5015', '-0.4744', '0.3818', '-0.4055', '0.1394', '0.466', '0.153', '-0.02644', '-0.3967', '0.11957', '-0.535']",C34766,0007341,D007873,,,10034735,
mondo:0007886,uterine corpus leiomyoma,"['fibroid of the uterine corpus', 'fibroid of corpus uteri', 'leiomyoma of the body of uterus', 'uterus fibroma', 'uterine corpus leiomyoma', 'corpus uteri leiomyoma', 'leiomyoma, uterine', 'uterine corpus fibroid', 'leiomyoma of body of uterus', 'fibroid of the uterine body', 'fibroid of body of uterus', 'corpus uteri fibroid', 'leiomyoma of the uterine corpus', 'fibroid of uterine body', 'uterine body leiomyoma', 'UL', 'fibroid of the corpus uteri', 'leiomyoma of the corpus uteri', 'leiomyoma of uterine corpus', 'leiomyoma of corpus uteri', 'uterine body fibroid', 'uterine fibroid', 'body of uterus leiomyoma', 'fibroid of uterine corpus', 'uterine leiomyoma', 'body of uterus fibroid', 'leiomyoma of uterine body', 'leiomyoma of the uterine body', 'plexiform leiomyoma', 'fibroid of the body of uterus', 'uterine corpus leiomyomata']",13223,150699,,C2242776,"['-0.3389', '0.0987', '0.08484', '-0.0642', '0.1603', '-0.10443', '0.1259', '0.03482', '-0.1135', '0.03192', '-0.173', '0.0709', '-0.05197', '0.0715', '-0.1826', '-0.1312', '-0.1846', '-0.10364', '-0.01316', '-0.3845', '0.02405', '-0.1406', '0.275', '-0.1417', '0.05945', '-0.1666', '0.05765', '-0.07825', '-0.0992', '-0.07574', '0.3418', '-0.00433', '0.1149', '-0.1017', '0.09814', '0.0743', '-0.1525', '0.1208', '0.0265', '-0.3257', '0.1263', '-0.2439', '-0.0718', '-0.0443', '-0.02751', '-0.2024', '-0.04297', '0.11786', '0.2399', '0.0957', '0.05338', '-0.1293', '0.0783', '0.07477', '-0.1501', '-0.11224', '0.1973', '0.03308', '-0.2573', '0.001305', '0.1412', '0.10187', '-0.0928', '-0.0203', '-0.1227', '0.05045', '0.2074', '0.2141', '-0.1757', '0.2822', '-0.01557', '-0.01942', '0.12244', '0.1448', '-0.0807', '-0.05878', '-0.0647', '0.183', '-0.03366', '-0.3242', '-0.176', '0.01602', '0.0696', '0.0394', '-0.2036', '-0.2141', '0.03848', '0.1842', '0.1396', '-0.1273', '0.1183', '0.1937', '0.02138', '0.0226', '0.3374', '-0.06085', '0.2236', '-0.2595', '-0.09937', '0.1212']",C7052,0000731,D047708,218.9,,,0000131
mondo:0007887,leiomyoma of vulva and esophagus,"['leiomyoma of vulva and esophagus', 'leiomyomatosis, esophagogastric and vulvar', 'esophagogastric and vulvar leiomyomatosis']",,150700,,C1835488,,,,C537006,,,,
mondo:0007888,hereditary leiomyomatosis and renal cell cancer,"['familial leiomyomatosis cutis et uteri', 'hereditary leiomyomatosis and renal cell cancer syndrome', 'hereditary leiomyomatosis and renal cell carcinoma', 'leiomyomatosis familial', 'multiple cutaneous leiomyomata', 'hereditary multiple cutaneous leiomyomas', 'familial leiomyomatosis with renal carcinoma', 'leiomyoma, multiple cutaneous', 'multiple cutaneous and uterine leiomyomata', 'multiple cutaneous and uterine leiomyomata 1, with or without renal cell carcinoma', 'familial multiple cutaneous leiomyomas', 'hereditary leiomyomatosis', 'leiomyomatosis and renal cell cancer, hereditary', 'hereditary leiomyomatosis with renal carcinoma', 'leiomyomatosis and renal cell cancer', 'familial leiomyomatosis', 'LRCC', 'HLRCC', 'familial leiomyomatosis and renal cell cancer', 'MCUL', 'Reed syndrome', 'multiple cutaneous and uterine leiomyomas', 'hereditary leiomyomatosis and renal cell cancer', 'Reed^s syndrome']",,150800,523,CN239164,"['0.1537', '0.1137', '-0.292', '0.4963', '0.592', '-0.2151', '0.532', '0.561', '-0.1257', '-0.0334', '0.4724', '-0.0742', '-0.44', '0.663', '-0.5435', '0.074', '-0.306', '-0.667', '-0.4998', '-0.3838', '0.0729', '-0.676', '-0.2428', '-0.0663', '0.2336', '-0.4744', '0.3403', '0.1186', '0.5293', '-0.1632', '0.66', '-0.607', '0.442', '-0.7314', '0.6055', '-0.401', '-0.835', '0.0475', '-0.303', '0.04007', '0.5615', '-0.3376', '0.308', '-0.0615', '-0.02863', '-0.255', '-0.4143', '-0.9062', '1.369', '-0.2217', '-0.1544', '-0.4512', '0.204', '-0.3713', '-0.2449', '0.2664', '-0.2013', '0.1611', '-1.0625', '-1.05', '0.648', '0.0444', '-0.3713', '-0.4011', '-0.2698', '0.4805', '0.3423', '0.3865', '0.2433', '0.7456', '0.284', '0.6323', '-0.2031', '-0.1581', '1.368', '0.2146', '0.1278', '-0.10925', '-0.21', '-0.046', '-0.2319', '0.61', '0.2205', '-0.3384', '-0.028', '0.1351', '0.731', '0.2537', '0.8037', '-0.2249', '0.1958', '0.1062', '0.05432', '0.3052', '-0.1071', '0.1243', '-0.275', '-0.564', '-0.4304', '-0.1246']",C51302,,C535516,,,,
mondo:0007890,"lentiginosis, centrofacial neurodysraphic","['lentiginosis, Touraine type', 'lentiginosis, centrofacial neurodysraphic']",,151000,,C1835484,,,,C563630,,,,
mondo:0007891,familial generalized lentiginosis,"['lentiginosis, generalized', 'familial lentigines profusa', 'lentiginosis, diffuse', 'lentiginosis, generalised', 'lentiginosis, inherited patterned', 'lentiginosis profusa', 'familial multiple lentigines syndrome without systemic involvement']",,151001,231040,CN201466,,,,C573023,,,,
mondo:0007892,Lenz-Majewski hyperostotic dwarfism,"['multiple congenital anomalies, mental retardation and progressive skeletal sclerosis', 'Lenz-Majewski syndrome', 'multiple congenital anomalies, intellectual disability and progressive skeletal sclerosis', 'Lenz Majewski hyperostotic dwarfism', 'hyperostotic dwarfism Lenz-Majewski type', 'LMHD', 'Lenz-Majewski hyperostotic dwarfism', 'Lenz-Majewski hyperostotic dysplasia']",0111507,151050,2658,,"['-0.2832', '0.2023', '-0.1052', '-0.5293', '0.4246', '0.01608', '-0.1675', '1.167', '-0.775', '-0.769', '0.02852', '-0.3118', '0.4062', '0.54', '-0.064', '-0.717', '0.649', '0.2455', '-0.4382', '-1.143', '-1.342', '0.193', '0.9526', '-0.1393', '0.1449', '-0.312', '-0.5044', '-0.2847', '0.584', '-0.093', '0.2191', '-0.5503', '-0.2205', '-0.0947', '-0.3438', '-0.59', '-0.02115', '0.1652', '0.3076', '-0.3118', '-0.0638', '0.3267', '-0.706', '-0.4197', '0.639', '-0.2478', '-0.07794', '0.2006', '0.514', '-0.3137', '-0.07153', '0.09406', '-0.3066', '0.4434', '-0.10834', '-1.02', '-0.6357', '-0.192', '0.8286', '0.2852', '-0.2144', '0.3252', '-0.10516', '0.259', '0.2151', '1.064', '-0.03598', '0.3408', '-0.3433', '0.502', '-0.5205', '-0.04703', '0.3293', '-1.123', '-0.2332', '0.408', '0.001532', '0.3904', '-0.1804', '-0.02347', '-0.593', '0.1552', '-0.1019', '0.0298', '0.3457', '-0.3154', '-0.0358', '-0.1873', '0.51', '0.438', '0.0512', '0.0665', '-0.4224', '-0.7773', '0.4734', '-0.2922', '-0.03467', '-0.06757', '0.908', '0.09753']",,,C537115,,,,
mondo:0007893,Noonan syndrome with multiple lentigines,"['lentigines, electrocardiographic conduction defects, 0cular hypertelorism, pulmonary stenosis, abnormalities of the genitals, retarded Growth, deafness', 'lentigines, electrocardiographic conduction abnormalities, ocular hypertelorism, pulmonic stenosis, abnormal genitalia, retardation of growth, Deafnes', 'Cardiomyopathic lentiginosis', 'LEOPARD syndrome', 'Gorlin syndrome II', 'generalised lentiginosis', 'lentiginosis profusa syndrome', 'Capute-Rimoin-Konigsmark-Esterly-Richardson syndrome', 'generalized lentiginosis', 'Moynahan syndrome', 'progressive cardiomyopathic lentiginosis', 'familial multiple lentigines syndrome']",14291,,500,CN074218,"['0.1562', '0.0716', '0.4985', '-0.563', '-0.11597', '0.11414', '0.3372', '1.156', '-0.571', '-0.764', '0.7324', '-0.3113', '0.1895', '0.1476', '-0.11285', '0.11237', '-0.4746', '-0.3713', '-0.676', '-0.2766', '0.00751', '0.2343', '0.01415', '-0.703', '0.2515', '-0.1698', '-0.7393', '0.3071', '1.189', '0.2428', '0.7627', '-0.7773', '0.484', '0.4424', '-0.2219', '-0.5034', '-0.2382', '0.6846', '0.2725', '-0.4712', '0.4932', '0.9043', '0.3438', '-0.1967', '-0.05914', '-0.2712', '-0.11804', '0.2161', '0.4417', '-0.083', '-0.3315', '0.1628', '-0.1759', '0.481', '-0.544', '-0.525', '-0.1248', '0.04578', '-0.0664', '-0.3782', '-0.11224', '-0.6333', '0.4778', '-0.0704', '0.558', '-0.2008', '-0.1664', '0.415', '0.1346', '0.7183', '0.05664', '0.2495', '-0.046', '0.2272', '0.5127', '0.2224', '0.3198', '0.0581', '0.0208', '-0.3057', '0.2864', '-0.4727', '0.01304', '-0.1162', '-0.2485', '-0.5654', '0.369', '-0.2031', '0.706', '0.946', '-0.1931', '0.352', '-0.377', '-0.275', '0.819', '-0.3357', '0.5527', '-0.1403', '0.0739', '0.0779']",C84820,,D044542,709.09,,10062901,
mondo:0007894,Leri pleonosteosis,"['leri pleonosteosis chromosome duplication syndrome', 'Leri pleonosteosis', 'pleonosteosis Leri type', 'Leri type pleonosteosis', 'chromosome 8q22.1 DUPLICATION syndrome', 'Leri^s pleonosteosis']",,151200,2900,C1835450,,,,C537118,,,,
mondo:0007895,"platyspondylic dysplasia, Torrance type","['Platyspondylic lethal skeletal dysplasia Torrance type', 'lethal short-limbed Platyspondylic dwarfism Torrance type', 'thanatophoric dysplasia Torrance variant', 'platyspondylic skeletal dysplasia, Torrance type', 'Platyspondylic lethal skeletal dysplasia, Luton type', 'thanatophoric dysplasia, Torrance variant', 'PLSD-T', 'lethal short-limbed Platyspondylic dwarfism, Torrance type', 'Platyspondylic dysplasia, Torrance-Luton type', 'thanatophoric dysplasia, Luton variant', 'PLSDT', 'Platyspondylic lethal skeletal dysplasia, Torrance type']",0111508,151210,85166,C1835437,"['-0.409', '0.0876', '0.224', '-0.3308', '0.2031', '-0.3372', '-0.03008', '0.584', '-0.3984', '-0.4707', '-0.11115', '-0.09515', '-0.1619', '-0.0163', '0.05765', '0.0718', '0.17', '-0.137', '-0.2615', '-0.3442', '0.1381', '-0.10254', '0.5957', '-0.1864', '0.3442', '0.1749', '-0.1149', '-0.0776', '0.0268', '-0.006252', '0.295', '-0.1976', '-0.0932', '0.103', '0.1521', '-0.3674', '-0.12305', '-0.4404', '0.07947', '-0.2474', '0.02292', '-0.3425', '0.0959', '-0.1311', '-0.1098', '-0.1102', '-0.1065', '0.2351', '0.06445', '-0.2312', '0.197', '-0.262', '-0.1588', '0.009186', '-0.233', '-0.5225', '0.06885', '-0.1338', '-0.01535', '0.1044', '0.2306', '0.0483', '-0.3147', '-0.02509', '-0.03302', '-0.2174', '0.0845', '0.2583', '-0.3767', '0.1764', '-0.313', '-0.02905', '0.3257', '0.08093', '-0.05432', '0.3113', '-0.2876', '0.1278', '-0.1498', '-0.271', '0.05685', '0.303', '0.1267', '0.2329', '-0.07324', '0.4597', '-0.05222', '0.3403', '0.12286', '0.005955', '-0.2793', '0.11914', '-0.00866', '0.0936', '0.564', '0.0796', '0.633', '-0.4045', '0.1481', '-0.0553']",,,C563627,,,,
mondo:0007896,acute monocytic leukemia,"['acute monocytic leukemia (FAB M5b)', 'acute monocytic leukemia', 'acute myeloblastic leukemia type 5', 'acute monocytic leukemia without mention of remission', 'monocytic leukemia, acute', 'acute monocytic leukemia, FAB M5', 'leukemia, acute monocytic', 'acute monocytic leukemia (FAB M5B)', 'acute monocytic leukaemia (FAB M5B)', 'acute monoblastic/monocytic leukemia', 'acute monoblastic/monocytic leukaemia', 'acute monoblastic leukemia and acute monocytic leukemia', 'AML-M5', 'acute myeloblastic leukaemia type 5', 'leukemia, monocytic, malignant', 'acute monocytic leukaemia (FAB M5b)', 'acute monocytic leukemia, morphology', 'acute monoblastic leukaemia and acute monocytic leukaemia', 'acute monocytic leukemia, morphology (morphologic abnormality)', 'acute monoblastic leukaemia', 'acute monocytic leukaemia without mention of remission', 'AML M5', 'monocytic leukaemia', 'acute monoblastic leukemia', 'monocytic leukemia']",8864,151380,514,C1318544,,C4861,0000221,D007948,206.0,,10059439,
mondo:0007898,"leukocyte nuclear appendages, hereditary prevalence of","['leukocyte nuclear appendages, hereditary prevalence of']",,151500,,C1835405,,,,C563626,,,,
mondo:0007899,lichen sclerosus et atrophicus,"['lichen sclerosus et atrophicus', 'lichen sclerosis', 'lichen sclerosis et atrophicus', 'lichen sclerosus', 'LSA', 'lichen SCLEROSUS ET ATROPHICUS']",,151590,33409,C0023652,,C26817,,D018459,,L90.0,,
mondo:0007900,nonsyndromic congenital nail disorder 3,"['porcelain nails', 'inherited isolated nail anomaly caused by mutation in PLCD1', 'leukonychia punctata', 'leukonychia Striatus', 'PLCD1 inherited isolated nail anomaly', 'nail disorder, nonsyndromic congenital, type 3', 'Gorlin Bushkell Jensen syndrome', 'NDNC3', 'nail disorder, nonsyndromic congenital, 3, (leukonychia)', 'nail disorder, nonsyndromic congenital, 3', 'leukonychia totalis multiple sebaceous cysts renal calculi', 'nonsyndromic congenital nail disorder type 3', 'leukonychia totalis and/or partialis']",0080081,151600,2387,,"['-0.122', '0.01531', '0.01527', '-0.1598', '0.3196', '-0.0689', '-0.2258', '0.00932', '-0.0595', '-0.1918', '-0.1368', '-0.02669', '-0.1926', '-0.03363', '-0.1615', '0.1194', '0.083', '-0.2632', '-0.1681', '-0.4927', '-0.1084', '-0.00461', '0.3738', '-0.1236', '0.2878', '0.093', '-0.1703', '0.07446', '0.193', '-0.2211', '0.2798', '-0.05286', '0.0696', '0.3145', '0.0614', '-0.1127', '-0.1984', '-0.0286', '-0.0055', '-0.27', '0.001982', '-0.1575', '0.2087', '-0.1678', '-0.0377', '-0.1183', '-0.0933', '0.01363', '-0.056', '-0.0578', '0.0689', '0.00945', '0.2522', '0.03845', '-0.3809', '-0.05176', '0.3403', '-0.259', '-0.3398', '-0.1212', '0.0737', '0.145', '-0.12396', '0.07263', '0.1694', '0.07', '0.3088', '0.4043', '0.00117', '0.4119', '-0.3013', '-0.2222', '-0.001434', '-0.0681', '-0.05273', '-0.02124', '0.2515', '0.06476', '-0.10333', '-0.2434', '-0.01532', '0.1202', '0.1691', '0.1414', '0.07104', '-0.01813', '-0.1968', '0.2773', '0.11945', '0.0166', '0.1422', '0.3435', '0.0947', '0.11865', '0.5474', '0.04034', '0.1164', '-0.2617', '0.1602', '0.2085']",,,C537289,703.8,,,
mondo:0007901,levator-medial rectus synkinesis,"['levator-medial rectus synkinesis', 'oculomotor-levator synkinesis']",,151610,,C1835403,,,,C563625,,,,
mondo:0007902,"lichen planus, familial","['lichen planus, familial', 'hereditary lichen planus']",,151620,,C1835402,,,,C563624,,,,
mondo:0007904,median nodule of the upper lip,"['LIP, MEDIAN NODULE of upper']",,151630,2699,C1835396,,,,,,,,
mondo:0007905,"lip, hamartomatous","['enlargement of Lower lip', 'lip, hamartomatous']",,151640,,C1835395,,,,C563621,,,,
mondo:0007906,"familial partial lipodystrophy, Dunnigan type","['reverse partial lipodystrophy', 'lipodystrophy, reverse partial', 'familial lipodystrophy of limbs and lower trunk', 'lipodystrophy, familial, of limbs and Lower trunk', 'familial partial lipodystrophy Dunnigan type', 'FPL2', 'familial partial lipodystrophy type 2', 'Dunnigan syndrome', 'FPLD2', 'lipodystrophy, familial partial, type 2', 'lipodystrophy, familial partial, Dunnigan type']",0070202,151660,2348,,"['0.732', '-0.004143', '-0.198', '-0.4683', '0.449', '-0.6133', '0.4177', '0.539', '-0.2186', '-0.2241', '-0.5117', '-0.27', '0.298', '0.3508', '-0.69', '-0.07935', '0.1175', '0.0447', '-0.3784', '-0.164', '-0.2588', '-0.607', '0.4912', '-0.10706', '-0.3652', '0.2233', '0.1641', '-0.3357', '0.279', '-0.722', '1.633', '-0.2507', '0.4146', '-0.283', '-0.437', '0.3809', '0.06885', '0.03035', '-0.07654', '-0.4082', '-0.635', '-0.261', '0.2449', '0.753', '0.7104', '-0.122', '-0.0846', '0.01747', '0.2383', '0.05008', '-0.1743', '-0.05', '0.52', '-0.2507', '-0.2385', '-0.2878', '0.4788', '-0.558', '-0.5415', '-0.326', '-0.3877', '-0.05988', '-0.02606', '-0.8916', '-0.597', '0.4492', '-0.1658', '-0.014984', '-0.1387', '-0.2153', '-0.1293', '-0.08606', '-0.02615', '-0.0517', '0.537', '-0.2925', '0.2395', '0.4883', '-0.0958', '-0.537', '-0.3176', '0.508', '0.09344', '-0.04208', '-0.1675', '0.555', '-0.0466', '-0.352', '0.6636', '0.236', '0.2275', '0.3599', '-0.03812', '0.3884', '0.7983', '-0.3635', '0.8384', '-0.218', '-0.4038', '-0.3743']",,,,,,,
mondo:0007907,lipoma of the conjunctiva,['lipoma of the conjunctiva'],,151700,,C1835373,,,,C563620,,,,
mondo:0007908,multiple symmetric lipomatosis,"['Madelung disease', 'multiple symmetrical lipomatosis', 'benign symmetrical lipomatosis', 'familial symmetric lipomatosis', 'lipodystrophy, cephalothoracic', 'MSL', 'multiple symmetric lipomatosis', 'Madelung^s neck', 'Launois-Bensaude lipomatosis', 'lipomatosis, familial benign cervical', 'Launois-Bensaude syndrome', 'Launois-Bensaude^s lipomatosis', 'Madelung^s disease', 'cervical symmetrical lipomatosis', 'lipomatosis, multiple symmetric', 'cephalothoracic lipodystrophy', 'familial benign cervical lipomatosis']",14116,151800,2398,CN201658,,C4392,1000737,,,,,
mondo:0007909,familial multiple lipomatosis,"['lipoma', 'lipomatosis, multiple', 'lipomatosis, familial multiple']",,151900,199276,,,,,D000071070,214.9,,,
mondo:0007910,lipoprotein types--Lt system,['lipoprotein types--Lt system'],,152300,,C1835359,,,,,,,,
mondo:0007911,"lipoprotein, variant of beta","['lipoprotein, variant of beta', 'Beta-lipoprotein, Double']",,152400,,,,,,,,,,
mondo:0007912,lithium transport,['lithium transport'],,152420,,,,,,,,,,
mondo:0007913,"low density lipoprotein, variation in molecular weight of","['LOW density lipoprotein, variation in molecular weight OF']",,152450,,,,,,,,,,
mondo:0007914,"lumbar stenosis, familial","['lumbar stenosis, familial']",,152550,,C1835320,,,,C563613,,,,
mondo:0007915,systemic lupus erythematosus,"['SLE', 'systemic lupus erythematosus (disease)', 'excess lymphocyte low molecular weight DNA', 'SLE - lupus erythematosus, systemic', 'lupus erythematosus, systemic', 'systemic lupus erythematosus, susceptibility to', 'disseminated lupus erythematosus', 'excess LMW-DNA', 'systemic lupus erythematosus', 'systemic lupus erythematosus susceptibility to', 'lupus nephritis, susceptibility to']",9074,152700,536,,"['0.4788', '-0.3137', '-0.2185', '0.091', '-0.09454', '-0.3103', '0.08014', '-0.0102', '-0.4875', '0.4329', '0.001081', '-0.1425', '0.03061', '-0.0892', '-0.2097', '-0.43', '0.03818', '0.5205', '-0.1978', '-0.661', '-0.2406', '-0.0464', '0.4924', '-0.7144', '-0.04904', '-0.355', '-0.1284', '0.2764', '-0.3474', '0.1287', '0.86', '-0.3086', '0.5093', '-0.3118', '0.11694', '0.02646', '-0.187', '0.169', '0.2485', '-0.3826', '0.03592', '-0.1683', '0.326', '-0.4902', '-0.02405', '0.01578', '0.1777', '-0.1494', '0.1626', '0.1658', '-0.1406', '0.04852', '0.5127', '0.01206', '-0.0817', '0.4524', '-0.3162', '0.316', '-0.3318', '-0.5786', '-0.099', '0.208', '-0.183', '-0.2546', '-0.5747', '-0.0978', '0.5293', '1.075', '-0.364', '0.65', '0.04266', '0.0867', '-0.1572', '-0.0945', '0.133', '0.3413', '0.3381', '0.959', '0.7544', '-0.6387', '-0.1749', '-0.3352', '-0.085', '-0.4568', '0.4658', '-0.4368', '-0.1301', '0.3052', '0.1962', '0.2058', '0.708', '-0.1029', '0.2678', '0.8057', '0.3127', '0.753', '-0.1365', '-0.2698', '-0.05603', '-0.289']",C3201,0002690,D008180,710.0,,,0002725
mondo:0007916,primary intestinal lymphangiectasia,"['lymphangiectasia, intestinal', 'Waldmann disease', 'primary intestinal lymphangiectasis', 'familial Waldmann^s disease (type)', 'Waldmann^s disease']",,152800,90362,CN206410,,,,,457.1,,,
mondo:0007917,lymphedema-cerebral arteriovenous anomaly syndrome,"['lymphedema and cerebral arteriovenous anomaly', 'primary pulmonary hypertension, cerebrovascular malformation and lymphedema feet']",,152900,86914,C1835272,,,,C563612,,,,
mondo:0007918,"microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability","['microcephaly with or without chorioretinopathy, lymphedema, or mental retardation', 'lymphedema and retinal Folds with microcephaly and microphthalmos', 'lymphedema, microcephaly and chorioretinopathy syndrome', 'microcephaly lymphedema chorioretinal dysplasia', 'lymphedema, microcephaly, chorioretinopathy syndrome', 'microcephaly and chorioretinopathy with or without mental retardation, autosomal dominant', 'microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability', 'microcephaly-lymphedema-chorioretinopathy syndrome', 'microcephaly and chorioretinopathy with or without intellectual disability, autosomal dominant', 'Cdmmr syndrome', 'chorioretinal dysplasia-microcephaly-mental retardation syndrome', 'MCLMR', 'microcephaly, lymphedema, chorioretinal dysplasia syndrome', 'lymphedema and retinal folds with ficrocephaly and microphthalmos', 'Mlcrd syndrome', 'chorioretinal dysplasia-microcephaly-intellectual disability syndrome', 'MLCRD']",0060349,152950,2526,C1835265,"['0.5557', '0.01967', '-0.2155', '-0.0797', '-0.183', '-0.543', '0.359', '0.3594', '-0.3325', '-0.554', '0.4014', '1.133', '0.1467', '0.4626', '-0.5093', '0.319', '-0.331', '-0.2742', '-0.09174', '-0.1527', '0.10297', '0.431', '-0.181', '-0.03244', '0.2052', '0.0772', '-0.4268', '0.6206', '0.6875', '0.01178', '-0.3293', '0.1855', '0.7764', '-0.1692', '0.3948', '0.2913', '-0.6055', '0.005497', '0.4954', '-0.07556', '0.632', '0.2146', '0.375', '-0.1726', '0.10443', '0.181', '-0.014824', '-0.546', '0.833', '-0.1846', '0.04254', '-0.2146', '0.3044', '0.1558', '-0.435', '-0.4963', '-0.06122', '-0.7075', '-0.4304', '-0.2659', '0.0454', '0.09375', '-0.4736', '0.2817', '-0.427', '0.5977', '0.269', '0.9434', '-0.848', '-0.03894', '-0.871', '0.2366', '-0.1432', '-0.03763', '0.2102', '0.1339', '-0.3826', '0.03017', '0.1776', '0.1048', '0.0429', '0.5596', '-0.109', '0.5684', '0.3816', '0.1584', '-0.8037', '-0.3955', '-0.1464', '0.2223', '0.1263', '1.016', '-0.1637', '0.3098', '1.462', '0.1482', '0.8115', '-0.2058', '0.3196', '-0.184']",,,C537711,,,,
mondo:0007919,lymphatic malformation 1,"['congenital primary lymphedema', 'LMPH1A', 'FLT4 hereditary lymphedema', 'congenital hereditary lymphedema', 'early onset lymphedema', 'Nonne-Milroy disease', 'hereditary lymphedema caused by mutation in FLT4', 'lymphedema, early-onset', 'lymphedema, hereditary, 1A', 'Nonne-Milroy syndrome', 'Nonne-Milroy lymphedema', 'primary congenital lymphedema', 'lymphedema, hereditary, type 1A', 'Nonne’s syndrome', 'Milroy disease', 'hereditary lymphedema type I', 'hereditary lymphedema 1']",0070212,153100,79452,,"['0.4722', '-0.3735', '-0.4329', '0.1687', '-0.1837', '-1.27', '0.3108', '0.1564', '-0.2275', '-0.2974', '0.4873', '1.259', '-0.07513', '1.049', '-0.554', '-0.04742', '-0.4546', '-0.1247', '-0.3462', '-0.2091', '0.1482', '-0.02135', '0.2295', '0.05832', '0.006657', '-0.0714', '-0.207', '0.865', '0.6304', '-0.065', '-0.4072', '0.2361', '0.4385', '-0.0692', '0.2201', '0.1912', '-0.3586', '-0.123', '1.004', '-0.528', '0.2673', '0.3364', '0.5596', '0.07446', '0.02605', '-0.1155', '-0.607', '-0.844', '1.389', '-0.10657', '0.01005', '-0.3037', '0.5005', '0.636', '-0.5215', '-0.323', '0.2756', '-0.7334', '-0.768', '-0.3965', '0.1004', '0.4368', '-0.426', '-0.03583', '-0.3962', '0.7104', '0.7905', '1.042', '-0.779', '-0.3574', '-0.7266', '0.4795', '-0.27', '-0.5103', '0.463', '0.1943', '-0.607', '0.973', '0.2517', '-0.4495', '-0.2615', '0.643', '-0.1962', '0.3594', '0.583', '-0.3396', '-0.3667', '-0.3086', '0.0894', '0.0758', '0.01717', '0.721', '-0.4224', '0.247', '1.224', '0.0841', '0.5537', '-0.3716', '0.0573', '0.05206']",,,,,,,
mondo:0007920,lymphatic malformation 5,"['hereditary lymphedema type II', 'late-onset lymphedema', 'lymphedema, hereditary, II', 'lymphedema, late-onset', 'Meige disease', 'Meige lymphedema', 'lymphedema preacox', 'late-onset primary lymphedema', 'lymphedema praecox', 'LMPH2', 'lymphedema hereditary type 2']",0070213,153200,90186,,,,,C562467,,,10027138,
mondo:0007921,yellow nail syndrome,"['yellow nail syndrome', 'lymphedema with yellow nails', 'YNS', 'lymphedema and Yellow nails', 'Yns']",0050468,153300,662,C0221348,,C85238,1001452,D056684,757.0,L60.5,10048244,
mondo:0007922,lymphedema-distichiasis syndrome,"['lymphedema-distichiasis syndrome with renal disease and diabetes mellitus', 'hereditary lymphedema-distichiasis syndrome (subtype)', 'lymphedema-distichiasis syndrome', 'lymphedema with distichiasis']",0111509,153400,33001,C0265345,"['0.5767', '-0.025', '-0.2178', '-0.02618', '-0.0638', '-0.773', '0.5605', '0.3218', '-0.2308', '-0.6953', '0.2827', '1.213', '0.3606', '0.6543', '-0.588', '0.1117', '-0.1898', '-0.1937', '-0.1924', '-0.2717', '0.05502', '0.2045', '0.0232', '0.1062', '0.0568', '0.1941', '-0.398', '0.5713', '0.6978', '0.01448', '-0.5996', '0.469', '0.8257', '-0.01967', '0.0208', '0.4946', '-0.05777', '-0.0667', '0.778', '-0.4722', '0.4412', '0.6836', '0.512', '0.248', '0.05188', '-0.1349', '-0.4163', '-0.796', '1.172', '-0.4534', '-0.0359', '-0.4075', '0.725', '0.1289', '-0.7944', '-0.04004', '0.02914', '-0.8325', '-0.5527', '-0.8203', '0.0434', '0.4104', '-0.4236', '-0.3564', '-0.365', '0.4246', '0.808', '1.027', '-0.749', '-0.2238', '-0.709', '0.1434', '0.0071', '-0.48', '0.706', '-0.1812', '-0.4688', '0.5234', '0.2717', '-0.1738', '-0.0316', '0.551', '0.1553', '0.621', '0.5083', '-0.2683', '-0.617', '-0.539', '-0.2329', '-0.001575', '0.2242', '0.875', '-0.0331', '0.2708', '1.487', '-0.1371', '0.705', '-0.3079', '0.2068', '-0.1003']",C128191,,C537710,743.63,Q82.0,,
mondo:0007923,"macrocephaly, benign familial","['benign familial megalencephaly', 'benign familial macrocephaly', 'Cole-Hughes syndrome', 'macrocephaly, benign familial']",,153470,,,,,,C537717,,,,
mondo:0007924,Bannayan-Riley-Ruvalcaba syndrome,"['Myhre-Riley-Smith syndrome', 'RMSS', 'Ruvalcaba -Myhre-Smith syndrome', 'RILEY-SMITH syndrome', 'BZS', 'Bannayan-Zonana syndrome', 'Riley-Smith syndrome', 'macrocephaly multiple lipomas and hemangiomata', 'Bannayan-Riley-Ruvalcaba syndrome', 'BRRS', 'Ruvalcaba-MYHRE-SMITH syndrome', 'macrocephaly with multiple lipomas and hemangiomas', 'Ruvalcaba-Myhre-Smith syndrome', 'macrocephaly pseudopapilledema and multiple hemangiomas', 'Bannayan syndrome', 'macrocephaly, pseudopapilledema, and multiple hemangiomata', 'macrocephaly, multiple lipomas, and hemangiomata']",0050657,153480,109,C0265326,,C3939,,,759.6,,,
mondo:0007925,myelodysplastic syndrome associated with isolated del(5q),"['5q syndrome', '5q- syndrome', 'refractory macrocytic anemia due to 5q deletion', '5Q minus syndrome', 'myelodysplastic syndrome with isolated del(5q)', '5q- syndrome, refractory macrocytic anemia due to 5q deletion', 'megakaryocytes, unilobular nucleated', '5q- syndrome, refractory macrocytic anaemia due to 5q deletion', '5Q- syndrome', 'macrocytic anemia, refractory, due to 5q deletion, somatic', 'chromosome 5q deletion syndrome', 'refractory macrocytic anaemia due to 5q deletion', '5q deletion syndrome', 'myelodysplastic syndrome associated with isolated del(5q) chromosome abnormality', 'macrocytic Anemia, refractory, due to 5Q deletion', 'MAR', 'myelodysplastic syndrome associated with isolated del (5q) chromosome Abnormality', 'myelodysplastic syndrome with 5q deletion']",0090016,153550,86841,CN206233,,C6867,,C535323,,,,
mondo:0007927,congenital macroglossia,['macroglossia'],,153630,2430,,,,,C531735,750.15,,,
mondo:0007930,"Bernard-Soulier syndrome, type A2, autosomal dominant","['BSSA2', 'Bernard-Soulier syndrome, type A2, autosomal dominant', 'Bernard-Soulier syndrome type A2', 'Bernard-Soulier syndrome, type A2 (dominant)']",0111059,153670,,C3277076,,,,,,,,
mondo:0007931,vitelliform macular dystrophy 2,"['Best macular dystrophy', 'macular dystrophy, vitelliform, 2', 'Best vitelliform macular dystrophy, multifocal', 'BVMD', 'BEST1 retinopathy', 'early-onset vitelliform macular dystrophy', 'vitelliform macular dystrophy, early-onset', 'BMD', 'macular degeneration, polymorphic vitelline', 'macular dystrophy, vitelliform, type 2', 'juvenile-onset vitelliform macular dystrophy', 'VMD2', 'polymorphic vitelline macular degeneration', 'vitelliform macular dystrophy, type 2', 'Best disease', 'vitelliform macular dystrophy, juvenile-onset', 'vitelliform macular dystrophy type 2', 'macular Degeneration, polymorphic vitelline']",,153700,1243,,"['-0.07434', '-0.2998', '-0.3127', '-0.08014', '0.271', '-0.1599', '-0.2437', '0.4949', '-0.2211', '-0.3403', '-0.187', '0.10645', '-0.2046', '0.6016', '-0.05777', '-0.651', '-0.1437', '-0.2164', '0.2239', '-0.4492', '-0.4773', '-0.383', '0.1836', '0.01039', '-0.5176', '0.006226', '-0.4219', '-0.5386', '-0.436', '0.7827', '1.072', '-0.2482', '0.3425', '-0.0349', '-0.03885', '0.1696', '0.4744', '0.0841', '0.02255', '-0.5703', '0.2372', '0.07245', '-0.0709', '-0.0322', '-0.2864', '0.1229', '-0.3574', '-0.471', '-0.010124', '-0.09796', '0.492', '-0.2913', '0.0784', '-0.302', '0.303', '0.377', '0.9766', '-0.2341', '-0.7397', '-0.386', '0.11273', '0.7314', '0.3503', '0.5903', '0.2308', '-0.01974', '0.8135', '0.2705', '0.08453', '0.5977', '-0.0791', '-0.6475', '0.395', '0.04376', '0.3276', '-0.4385', '0.06934', '0.00525', '-0.2456', '-0.9707', '0.665', '-0.4392', '0.2534', '0.7954', '-0.456', '0.0655', '0.011856', '-0.2698', '0.5493', '0.3967', '0.1009', '0.1372', '-0.4836', '0.4917', '0.618', '-0.4412', '0.33', '-0.3884', '-0.3394', '-0.0003994']",,,,,H35.5,,
mondo:0007932,age related macular degeneration 2,"['macular Degeneration, Senile', 'macular degeneration, age-related, 2', 'ARMD2', 'age related macular degeneration type 2', 'macular Degeneration, age-related, type 2', 'maculopathy, age-related, 2']",0110015,153800,,C3495438,,,,C562479,,,,
mondo:0007933,vitelliform macular dystrophy 1,"['VMD1', 'macular dystrophy, atypical vitelliform', 'macular dystrophy, vitelliform, 1', 'vitelliform macular dystrophy, atypical']",,153840,,,,,,C537832,,,,
mondo:0007934,benign concentric annular macular dystrophy,"['maculopathy, bull^s eye', 'macular dystrophy, concentric annular', 'Mcdca', 'retinitis pigmentosa 91', 'macular dystrophy, benign concentric annular']",,153870,251287,C4304667,,,,C537833,,H35.5,,
mondo:0007935,cystoid macular edema,"['cystoid macular dystrophy', 'macular edema, cystoid', 'autosomal dominant cystoid macular oedema', 'familial macular edema', 'macular dystrophy, dominant cystoid', 'familial macular oedema', 'Mddc', 'autosomal dominant cystoid macular edema', 'DCMD']",4447,153880,75381,C0730317,,C34794,,,,H35.5,,
mondo:0007936,"macular dystrophy, fenestrated sheen type","['macular dystrophy, fenestrated sheen type']",,153890,,C1835173,,,,C563607,,,,
mondo:0007937,renal hypomagnesemia 2,"['isolated autosomal dominant hypomagnesemia', 'magnesium loss, isolated renal', 'HOMG2', 'magnesium wasting, renal', 'isolated renal magnesium wasting', 'renal hypomagnesemia type 2', 'autosomal dominant primary hypomagnesemia with hypocalciuria', 'hypomagnesemia 2, renal', 'primary hypomagnesemia caused by mutation in FXYD2', 'FXYD2 primary hypomagnesemia', 'FXYD2 familial primary hypomagnesemia']",0060885,154020,34528,C4511005,"['-0.3708', '0.006', '-0.1472', '-0.514', '-0.04562', '-0.1246', '-0.618', '0.5283', '-0.7607', '0.1608', '-0.9106', '0.0904', '-0.3997', '0.633', '-0.11255', '0.3816', '-0.0532', '-0.157', '0.0381', '-0.5693', '-0.01418', '-0.4526', '0.1296', '0.10645', '0.4822', '0.1813', '-0.116', '-0.4866', '-0.0555', '-0.2642', '0.3352', '-0.09503', '0.3728', '-0.4897', '-0.3335', '-0.2568', '-0.0901', '-0.05676', '-0.3748', '0.115', '0.542', '-0.842', '0.3447', '-0.57', '-0.5547', '-0.344', '-0.5664', '-0.3853', '-0.009254', '0.806', '0.1917', '-0.131', '0.7876', '0.0909', '-0.352', '-0.6714', '0.8564', '-0.3264', '-0.1056', '0.3914', '0.5786', '-0.2705', '-0.00639', '-0.0641', '-0.2693', '-0.5312', '0.223', '0.4062', '-0.04648', '-0.3496', '-0.3005', '-0.1428', '0.1284', '0.01608', '0.804', '0.81', '-0.00924', '0.5635', '0.2756', '0.08954', '0.11865', '0.4634', '0.3625', '0.2029', '0.329', '0.3037', '-0.085', '0.2054', '0.2869', '-0.01775', '-0.1354', '0.0979', '-0.0503', '-0.8096', '1.052', '-0.415', '0.4436', '-0.661', '0.10156', '0.1785']",,,C537152,,,,
mondo:0007938,"46,XY sex reversal 4","['SRXY4', '46,XY SEX reversal 4', '46,XY sex reversal 4', 'chromosome 9P24.3 deletion syndrome', '46,XY Sex reversal type 4', '46,XY gonadal dysgenesis, partial or complete, with 9P24.3 deletion', '46XY sex reversal 4, Isolated cases']",0111771,154230,,,,C132270,,C567887,,,,
mondo:0007939,"malignant hyperthermia, susceptibility to, 2","['malignant hyperthermia susceptibility type 2', 'malignant hyperthermia susceptibility 2', 'malignant hyperthermia, susceptibility to, type 2', 'malignant hyperthermia, susceptibility to, 2', 'MHS2', 'malignant hyperpyrexia susceptibility type 2', 'Mhs2']",,154275,,,,,,C535695,,,,
mondo:0007940,"malignant hyperthermia, susceptibility to, 3","['Mhs3', 'malignant hyperthermia susceptibility type 3', 'malignant hyperpyrexia susceptibility type 3', 'malignant hyperthermia susceptibility 3', 'malignant hyperthermia, susceptibility to, 3', 'MHS3', 'malignant hyperthermia, susceptibility to, type 3']",,154276,,,,,,C535696,,,,
mondo:0007941,malocclusion due to protuberant upper front teeth,['malocclusion due to protuberant upper front teeth'],,154300,,,,,,,,,,
mondo:0007942,Mammastatin,['Mammastatin'],,154370,,,,,,C060120,,,,
mondo:0007943,Nager acrofacial dysostosis,"['split hand deformity-mandibulofacial dysostosis', 'preaxial manibulofacial dysostosis', 'mandibulofacial dysostosis with preaxial limb anomalies', 'NAFD', 'AFD, Nager type', 'mandibulofacial dysostosis, Treacher Collins type, with limb anomalies', 'Nager acrofacial dysostosis', 'preaxial acrofacial dysostosis', 'Nager acrofacial dysostosis syndrome', 'AFD1', 'preaxial acrodysostosis', 'AFD', 'Nager syndrome', 'acrofacial dysostosis 1, Nager type']",5768,154400,245,C0265245,"['0.1013', '0.04346', '0.3218', '-0.5825', '0.163', '-0.448', '0.6807', '0.2776', '-0.8936', '-1.011', '0.3142', '-0.862', '0.2015', '-0.02345', '0.151', '0.1087', '0.5186', '-0.2786', '-0.3093', '-0.177', '-0.1387', '-0.0643', '0.3647', '0.0685', '0.1555', '0.333', '-0.1622', '0.1698', '0.4468', '0.2659', '0.3926', '0.01686', '-0.3438', '-0.5103', '0.00604', '-0.266', '-0.05374', '-0.04755', '-0.717', '-0.1964', '0.2163', '-0.03625', '0.2659', '-0.1273', '-0.1671', '-0.6626', '-0.3997', '-0.203', '-0.0373', '0.304', '-0.619', '-0.5645', '-0.1373', '-0.1058', '-0.1041', '-0.3987', '0.2659', '-0.00961', '-0.007866', '0.2096', '-0.3706', '0.3533', '0.12396', '0.02193', '-0.4668', '-0.007553', '0.04846', '0.3003', '-0.1772', '0.2048', '-0.5244', '0.1941', '-0.00214', '0.2015', '0.3025', '0.5415', '0.1008', '-0.7935', '-0.6694', '0.1399', '0.2002', '0.03494', '0.645', '0.7915', '-0.506', '0.00832', '0.2361', '1.048', '-0.002676', '0.2457', '-0.977', '0.3367', '-0.2057', '0.292', '1.189', '-0.1597', '0.574', '-0.9033', '0.2542', '-0.144']",,,C538184,,,,
mondo:0007944,Treacher Collins syndrome 1,"['Treacher Collins syndrome type 1', 'TCS1', 'Treacher-Collins syndrome caused by mutation in TCOF1', 'mandibulofacial dysostosis', 'TREACHER COLLINS syndrome 1', 'Treacher Collins-Franceschetti syndrome', 'Treacher Collins syndrome', 'TCOF1 Treacher-Collins syndrome']",0080789,154500,,CN119605,,,,,,,,
mondo:0007945,"mannose 6-phosphate receptor recognition defect, Lebanese type","['phosphodiester glycoside deficiency', 'mannose 6-phosphate receptor recognition defect, Lebanese type']",,154570,,C1835134,,,,C563601,,,,
mondo:0007946,jaw-winking syndrome,"['jaw-winking syndrome', 'jaw-winking', 'mandibulo-palpebral synkinesis-ptosis syndrome', 'abnormal innervation syndrome of eyelid', 'Marcus-Gunn phenomenon', 'Marcus Gunn syndrome', 'jaw-blinking', 'pterygoid-levator synkinesis', 'familial Marcus Gunn phenomenon (subtype)', 'Marcus-Gunn syndrome', 'Maxillopalpebral synkinesis', 'Marcus Gunn phenomenon']",560,154600,91412,C0266521,,,,C535908,742.8,,10064583,
mondo:0007947,Marfan syndrome,"['Marfan^s syndrome', 'MFS', 'MFS1', 'Marfan syndrome type 1', 'Marfan syndrome', 'Marfan syndrome, type 1']",14323,154700,558,CN202883,"['-0.2235', '0.2998', '-0.1953', '0.2393', '0.264', '-0.526', '0.1707', '1.082', '-0.8623', '-0.7954', '0.2708', '-0.549', '0.3538', '0.6763', '-0.7246', '-0.2065', '-0.1312', '0.1322', '-0.2356', '-0.2754', '-0.00995', '0.757', '0.745', '-0.0866', '-0.4292', '0.512', '0.0857', '0.7227', '1.075', '0.8564', '1.177', '-0.0843', '0.972', '0.5073', '0.4202', '-0.4614', '0.3335', '-0.1738', '0.405', '-0.928', '0.3801', '0.663', '0.006855', '0.1697', '0.3813', '0.01904', '-0.10266', '0.2247', '0.3535', '-0.4734', '0.3042', '0.2524', '0.989', '-0.742', '0.001434', '-0.8794', '0.02875', '0.753', '0.2115', '-0.1987', '0.619', '0.2815', '-0.3083', '0.2418', '0.1266', '1.002', '0.001293', '0.3564', '-0.312', '0.1844', '0.1652', '0.206', '-0.04938', '-0.6777', '0.1755', '0.04562', '-0.449', '0.4932', '0.07434', '-0.6226', '0.375', '-0.5176', '0.2527', '-0.10333', '-0.1236', '0.1418', '0.01181', '0.5605', '-0.195', '0.2644', '-0.4678', '-0.2063', '-0.671', '-0.3489', '0.594', '-0.528', '0.9893', '-0.4502', '-0.181', '0.2205']",C34807,,D008382,759.82,,10026829,
mondo:0007948,marfanoid hypermobility syndrome,['marfanoid hypermobility syndrome'],,154750,,C0268365,,,,C531742,,,,
mondo:0007949,Marshall syndrome,"['Marshall syndrome', 'deafness, myopia, cataract, saddle nose-Marshall type', 'MRSHS']",0111510,154780,560,C0265235,"['-0.2961', '0.341', '0.4612', '-0.4517', '0.4116', '-0.5376', '0.003925', '0.2869', '-0.3542', '-0.395', '0.10004', '-0.2979', '-0.3997', '-0.1263', '-0.2622', '-0.2017', '0.2379', '0.2262', '-0.3938', '-0.4312', '0.1671', '-0.1432', '0.264', '0.1967', '0.296', '0.2869', '-0.0695', '-0.254', '0.592', '-0.03946', '-0.1792', '0.01197', '-0.06213', '-0.001398', '0.3936', '-0.2668', '-0.296', '-0.2292', '-0.157', '-0.5093', '0.1964', '-0.226', '-0.04587', '0.008865', '-0.269', '-0.4548', '-0.06573', '0.0569', '0.396', '-0.3472', '-0.2206', '0.1312', '0.121', '-0.05298', '0.05078', '-0.645', '0.0753', '-0.01057', '-0.1173', '-0.00991', '0.581', '0.0008297', '-0.3708', '0.2986', '-0.0884', '-0.0979', '-0.1696', '0.459', '-0.2703', '0.3245', '-0.585', '0.02028', '0.2512', '-0.02121', '-0.3372', '-0.0266', '0.1746', '0.569', '0.0433', '0.1812', '0.04312', '-0.01178', '-0.1925', '0.6846', '-0.484', '0.1687', '0.0642', '1.013', '0.2668', '0.537', '-0.299', '0.4119', '0.36', '0.137', '0.939', '-0.1432', '0.5513', '-0.41', '0.2666', '0.2712']",C128115,,C536025,759.89,,,
mondo:0007950,mastocytosis,"['urticaria pigmentosa', 'mast cell hyperplasia', 'Mast cell disease', 'MAST cell disease', 'mastocytosis']",350,,98292,C0024899,,C84269,,D008415,,,10026891,
mondo:0007951,"masticatory muscles, hypertrophy of","['masseter muscle Hypertrophy', 'masticatory muscles, hypertrophy of']",,154850,,,,,,C563600,,,,
mondo:0007952,maxillofacial dysostosis,['maxillofacial dysostosis'],,155000,,C1835088,,,,C563599,,,,
mondo:0007953,Binder syndrome,"['binder syndrome', 'MAXILLONASAL dysplasia, BINDER type', 'maxillonasal dysplasia', 'Binder syndrome', 'Maxillonasal dysostosis', 'binder type maxillonasal dysplasia']",14683,155050,1248,C0220692,,,,C536036,,,,
mondo:0007955,Meckel diverticulum,"['Meckel diverticulum', 'Meckel^s diverticulum', 'persistent vitelline duct']",9487,155140,,,,C12264,1001036,D008467,751.0,,10027055,
mondo:0007956,Pai syndrome,"['Pai syndrome', 'cleft, Median, of upper lip with polyps of Facial skin and nasal mucosa', 'median cleft of upper lip with polyps of facial skin and nasal mucosa', 'median cleft of the upper lip-corpus callosum lipoma-cutaneous polyps syndrome', 'cleft, MEDIAN, of upper LIP with polyps of facial skin and nasal mucosa']",,155145,1993,C1835087,,,,C536135,,,,
mondo:0007957,mediosternal depigmentation line,['mediosternal depigmentation line'],,155200,,,,,,,,,,
mondo:0007958,familial medullary thyroid carcinoma,"['Mtc1', 'Fmtc', 'thyroid carcinoma, familial medullary', 'familial MTC', 'hereditary medullary thyroid gland carcinoma', 'MTC', 'hereditary thyroid medullary carcinoma', 'medullary thyroid carcinoma']",0050547,155240,99361,C1833921,"['-0.0423', '0.2294', '-0.0701', '0.05447', '0.1033', '-0.1526', '-0.03986', '0.05905', '-0.1389', '-0.2212', '0.1923', '-0.0823', '0.02097', '-0.10004', '-0.221', '-0.2196', '-0.0318', '-0.1082', '-0.02121', '-0.421', '0.01176', '-0.06683', '0.2247', '-0.2037', '0.2883', '0.0397', '0.1346', '0.02856', '0.0861', '-0.1809', '0.2456', '0.0315', '0.1527', '-0.1091', '-0.09546', '-0.08417', '0.0251', '-0.04355', '0.00316', '-0.1183', '0.1282', '-0.1799', '0.2208', '-0.1337', '0.1201', '-0.1921', '-0.004223', '-0.01611', '0.3022', '-0.05676', '0.02336', '0.0319', '0.002768', '0.04337', '-0.2024', '-0.2411', '0.1891', '0.02798', '-0.4258', '0.003471', '0.3806', '0.05768', '0.0792', '-0.0817', '-0.01211', '0.1931', '0.334', '0.2295', '-0.288', '0.2247', '-0.2737', '-0.0565', '0.1804', '-0.0803', '0.11053', '0.2351', '-0.1112', '0.1222', '-0.2917', '-0.1873', '-0.1903', '0.2051', '-0.0892', '-0.07526', '-0.1326', '-0.0703', '0.1962', '-0.03735', '0.2272', '-0.03732', '-0.0759', '0.175', '0.04318', '-0.12476', '0.3096', '0.0778', '0.2473', '-0.2524', '-0.1543', '0.10187']",,,C536911,,,,
mondo:0007959,medulloblastoma,"['medulloblastoma, autosomal recessive, autosomal dominant, somatic mutation', 'cerebellar medulloblastoma', 'cerebellum embryonal neoplasm', 'medulloblastoma, desmoplastic, autosomal recessive, autosomal dominant, somatic mutation', 'medulloblastoma, somatic', 'medulloblastomas', 'infratentorial primitive neuroectodermal tumor', 'infratentorial primitive neuroectodermal tumour', 'localised primitive neuroectodermal tumour', 'localized primitive neuroectodermal tumor', 'medulloblastoma', 'brain medulloblastoma', 'medulloblastoma, desmoplastic', 'CPNET', 'MDB', 'medulloblastoma with extensive nodularity', 'CNS PNET', 'medulloblastoma, malignant']",0060104,155255,616,C1334410,"['0.297', '0.07385', '0.02017', '0.2072', '0.09454', '-0.1733', '0.3342', '0.7197', '-0.6655', '0.3438', '-0.06445', '0.01596', '-0.26', '0.09326', '0.4165', '0.1573', '-0.6875', '-0.6914', '0.02525', '-0.03864', '0.2576', '-0.2727', '0.5996', '-0.3252', '0.2686', '-0.1711', '0.24', '-0.1426', '-0.1934', '-0.1244', '0.2397', '0.0484', '0.611', '-0.1771', '-0.2834', '0.1997', '-0.4695', '-0.1184', '-0.3699', '-0.1757', '-0.06323', '0.0099', '0.619', '-0.6094', '0.2598', '0.08057', '-0.5537', '0.1522', '0.4304', '0.10284', '-0.141', '0.1295', '-0.4868', '-0.3384', '0.05246', '-0.1149', '0.2886', '0.3203', '-0.6514', '0.8057', '0.2896', '0.453', '-0.3672', '0.2086', '-0.1925', '0.03668', '-0.4495', '0.1311', '-0.1815', '0.5977', '0.3977', '0.773', '-0.0476', '0.03265', '0.3562', '-0.00417', '0.1969', '-0.0538', '-0.134', '-0.834', '-0.57', '-0.4272', '-0.239', '0.6045', '-0.503', '-0.08014', '0.8', '0.0289', '0.2148', '-0.2866', '0.4124', '0.2375', '-0.08356', '-0.792', '0.7983', '-0.1622', '0.7065', '0.1781', '-0.313', '0.11926']",C3222,0002939,D008527,,,10027107,
mondo:0007961,"megalencephaly, autosomal dominant","['megalencephaly, autosomal dominant']",,155350,,C3805727,,,,,,,,
mondo:0007962,megalodactyly,"['macrodactyly, somatic, (3), cerebral cavernous malformations 4, somatic', 'macrodactyly', 'Megalodactyly']",,155500,,,"['0.002016', '0.006126', '-0.001828', '-0.00759', '-0.0103', '0.005013', '-0.00423', '0.006832', '-0.000532', '-0.01018', '-0.002249', '0.00606', '-0.004753', '-0.00612', '0.00878', '-0.00585', '-0.000853', '0.006844', '0.00256', '-0.012314', '0.002344', '-0.003454', '0.001306', '-0.004597', '-0.006676', '0.002396', '0.007328', '0.001605', '-0.002169', '-0.005573', '-0.008644', '-0.008415', '0.001695', '-0.000633', '-0.005352', '-0.004803', '0.002476', '0.009705', '-0.00763', '0.001218', '0.003368', '0.00401', '-0.00815', '0.006676', '0.004898', '-0.00839', '-0.001955', '-0.005432', '0.010124', '-0.00791', '-0.001123', '-0.008705', '0.00015', '0.00811', '-0.01025', '0.00892', '0.000781', '-0.00884', '-0.007317', '-0.00621', '0.003052', '-0.00926', '-0.005527', '-0.002422', '0.004013', '-0.00537', '0.00929', '0.00842', '0.0001688', '0.000607', '-0.00879', '0.009926', '0.003498', '0.00426', '-0.002123', '0.001781', '-0.004078', '-0.003601', '-0.001364', '0.00979', '0.004635', '0.000943', '-0.006756', '0.008766', '-0.01042', '0.007687', '-0.003632', '-0.00326', '0.00961', '0.00576', '0.007206', '-0.003132', '-0.00859', '-0.003206', '-0.00653', '0.005466', '0.002523', '0.002787', '-0.00803', '0.004444']",C48900,,C562546,,,,
mondo:0007963,"melanoma, cutaneous malignant, susceptibility to, 1","['melanoma, cutaneous malignant', 'familial atypical Mole-malignant melanoma syndrome', 'dysplastic Nevus syndrome, hereditary', 'melanoma, cutaneous malignant, susceptibility to, 1', 'CMM1', 'melanoma, malignant', 'melanoma, malignant, somatic', 'B-K Mole syndrome', 'melanoma, cutaneous malignant, 1', 'melanoma, familial']",,155600,,C0151779,,,,,,,,
mondo:0007964,"melanoma, cutaneous malignant, susceptibility to, 2","['familial dysplastic nevi', 'CMM2', 'melanoma, cutaneous malignant, susceptibility to, 2', 'dysplastic nevus syndrome', 'melanoma, cutaneous malignant, 2', 'B-K Mole syndrome', 'Atypical Mole syndrome', 'susceptibility to cutaneous malignant melanoma 2', 'melanoma, cutaneous malignant, susceptibility to, type 2']",10041,155601,,,,C7584,0004199,D004416,,,,
mondo:0007965,"melanoma, malignant familial intraocular","['melanoma, malignant familial intraocular']",,155700,,C1835043,,,,C563596,,,,
mondo:0007966,susceptibility to uveal melanoma,,,,,,,,,,,,,
mondo:0007967,melanoma and neural system tumor syndrome,"['melanoma astrocytoma syndrome', 'melanoma and neural system tumor syndrome', 'melanoma-astrocytoma syndrome']",0111511,155755,252206,C1835042,,,,C536149,,,,
mondo:0007968,melanoma tumor antigen Gp90,"['melanoma tumor antigen Gp90', 'Class 1 unique tumor antigen of melanoma', 'Class 1 unique tumour antigen of melanoma']",,155770,,,,,,,,,,
mondo:0007969,Melkersson-Rosenthal syndrome,"['Melkersson syndrome', 'Melkersson-Rosenthal syndrome', 'cheilitis Granulomatosa', 'Mros', 'cheilitis granulomatosa of Mescher-Melkersson-Rosenthal', 'Melkersson^s syndrome', 'MRS']",1761,155900,2483,C0025235,,C84886,1001039,D008556,,,10027166,
mondo:0007970,melorheostosis,"['Mel', 'melorheostosis, isolated, somatic mosaic', 'melorheostosis, isolated']",4253,155950,2485,C0025239,,C84887,,D008557,756.89,,10050284,
mondo:0007971,delayed membranous cranial ossification,"['Gonzales-del Angel syndrome', 'membranous cranial ossification, delayed']",,155980,3034,C1835030,,,,C563592,,,,
mondo:0007972,Meniere disease,"['Mnire^s vertigo', 'otogenic vertigo', 'Meniere disease', 'Meniere^s disease']",9849,156000,45360,C0025281,,C185243,0006862,D008575,386.00,,,
mondo:0007973,mental and growth retardation with amblyopia,['mental and growth retardation with amblyopia'],,156190,,C1835028,,,,C563591,,,,
mondo:0007974,"intellectual disability, autosomal dominant 1","['intellectual disability, autosomal dominant type 1', 'MBD5 autosomal dominant non-syndromic intellectual disability', 'MRD1', 'autosomal dominant non-syndromic intellectual disability caused by mutation in MBD5', 'chromosome 2Q23.1 deletion syndrome', 'autosomal dominant non-syndromic intellectual disability 1', 'mental retardation, autosomal dominant type 1', 'autosomal dominant intellectual disability 1', 'intellectual disability, autosomal dominant 1', 'mental retardation, autosomal dominant 1', 'autosomal dominant mental retardation 1']",0070031,156200,228402,,"['-0.6357', '0.7383', '0.8086', '-0.1971', '-0.344', '-0.454', '0.2291', '0.818', '-0.4585', '-0.4006', '-0.3894', '-0.4834', '0.3105', '-0.2146', '0.198', '0.827', '0.3035', '-0.2842', '-0.4153', '-0.2473', '-0.0696', '0.08997', '0.2622', '-0.231', '0.447', '-0.4082', '-0.266', '0.05487', '0.4438', '-0.3826', '0.224', '-0.602', '0.726', '0.2617', '-0.02594', '-0.1385', '-0.10596', '-0.2323', '0.10333', '-0.3445', '0.2261', '-0.7065', '-0.3914', '0.3606', '0.3625', '-0.6606', '-0.2534', '0.298', '-0.1729', '0.1831', '-0.65', '0.603', '-0.766', '0.4275', '-0.063', '-0.3625', '-0.1465', '-0.349', '0.3484', '-0.2646', '0.1975', '-0.11285', '-0.596', '0.2969', '-0.4468', '-0.007328', '0.01639', '0.2449', '-0.2322', '0.3706', '-0.5137', '0.3606', '0.194', '0.5645', '-0.2646', '0.6147', '0.10376', '-0.3496', '-0.2401', '0.4329', '0.05493', '-0.013916', '0.1958', '0.652', '0.5327', '0.651', '0.03876', '0.8613', '0.6846', '0.2976', '0.004547', '0.2917', '-0.3875', '-0.11005', '0.782', '0.4675', '0.10455', '-0.8413', '0.7793', '0.1831']",C141424,,C566947,,,,
mondo:0007975,"meralgia paraesthetica, familial","['meralgia paraesthetica, familial']",,156220,,C1835026,,,,C563590,,,,
mondo:0007976,mesomelic dwarfism of hypoplastic tibia and radius type,['mesomelic dwarfism of hypoplastic tibia and radius type'],,156230,,C1835010,,,,C563589,,,,
mondo:0007977,"mesomelic dysplasia, Kantaputra type","['mesomelic dysplasia Kantaputra type', 'mesomelic dysplasia, Thai type', 'mesomelic dysplasia Thai type', 'mesomelic dysplasia with ankle, carpal, and tarsal synostosis', 'MMDK', 'Mdk', 'mesomelic dysplasia, Kantaputra type', 'MDK', 'mesomelic dysplasia with ankle carpal and tarsal synostosis', 'Kantaputra mesomelic dysplasia']",,156232,1836,,,,,C535547,,,,
mondo:0007979,metachondromatosis,"['METACHONDROMATOSIS', 'metachondromatosis', 'METCDS']",0111512,156250,2499,C0410530,"['-0.8027', '-0.1392', '0.06995', '-0.3337', '0.071', '-0.8027', '0.314', '0.793', '-0.3293', '-0.5537', '0.1829', '0.3481', '-0.1879', '0.444', '0.1842', '0.276', '0.3499', '-0.03604', '0.2036', '-0.4895', '0.0005636', '-0.243', '0.6924', '-0.1569', '0.05844', '0.2644', '-0.2352', '0.2216', '-0.3416', '0.518', '0.1792', '-0.5356', '-0.1808', '-0.0006423', '-0.0731', '0.1847', '-0.173', '-0.4775', '0.3845', '0.367', '0.314', '-0.2262', '0.0531', '-0.1475', '0.533', '-0.1337', '-0.2515', '0.2725', '0.0786', '0.2311', '0.0557', '-0.225', '0.03023', '-0.1027', '-0.719', '-0.2012', '-0.0449', '0.247', '-0.286', '0.1914', '0.688', '-0.0771', '-0.5474', '-0.01536', '0.00834', '0.1223', '0.2084', '0.4458', '0.1858', '-0.2311', '0.1658', '-0.4983', '0.02095', '-0.1254', '0.1549', '0.4521', '-0.02188', '0.5215', '-0.1968', '-0.49', '-0.4053', '-0.004997', '0.336', '0.233', '-0.1964', '-0.263', '-0.3154', '-0.0743', '0.006947', '-0.1826', '-0.01369', '0.3318', '-0.2457', '0.201', '0.5503', '0.03293', '0.88', '-1.324', '0.4883', '0.3596']",,,C562938,756.59,,,
mondo:0007980,metachromasia of fibroblasts,['metachromasia of fibroblasts'],,156300,,,,,,,,,,
mondo:0007982,"metaphyseal chondrodysplasia, Jansen type","['murk Jansen type metaphyseal chondrodysplasia', 'Jansen type metaphyseal chondrodysplasia', 'Jansen disease', 'metaphyseal chondrodysplasia murk Jansen type', 'Jansen metaphyseal chondrodysplasia', 'Jansen metaphyseal dysostosis', 'metaphyseal chondrodysplasia, Jansen type', 'metaphyseal chondrodysplasia, murk Jansen type', 'Jansen^s metaphyseal chondrodysplasia']",0080020,156400,33067,C0265295,"['-0.4016', '0.275', '0.3037', '-0.48', '-0.00534', '-0.1493', '-0.2269', '0.5327', '-0.8267', '-0.4275', '0.01901', '0.574', '-0.2119', '0.01614', '0.1647', '-0.0941', '0.2998', '-0.0429', '0.1057', '-0.48', '0.03418', '-0.3506', '0.423', '-0.06976', '0.1733', '0.3262', '0.4548', '-0.10645', '0.4004', '-0.3809', '-0.283', '-0.2751', '0.02136', '-0.03049', '0.1472', '-0.184', '-0.1449', '0.011246', '0.1077', '-0.2544', '-0.0455', '-0.6426', '0.2195', '0.2327', '-0.07983', '-0.205', '-0.1654', '0.6494', '0.524', '0.0406', '-0.2864', '0.2798', '-0.02827', '0.304', '-0.5483', '-0.668', '-0.2803', '-0.2627', '0.1287', '0.5166', '0.4807', '0.02834', '-0.4268', '-0.2369', '0.01172', '0.2426', '0.0663', '0.4812', '0.02405', '0.06088', '-0.3416', '0.04156', '0.5337', '0.09204', '0.04626', '0.5127', '-0.1166', '0.1528', '-0.0648', '-0.02853', '-0.3643', '0.1263', '0.1973', '-0.1997', '-0.1362', '0.2705', '0.077', '0.03812', '0.661', '0.351', '-0.1382', '0.1537', '-0.1052', '-0.3635', '0.434', '0.2408', '0.7715', '-0.3682', '0.0008416', '0.2484']",C131868,,C537564,,,,
mondo:0007983,Schmid metaphyseal chondrodysplasia,"['metaphyseal chondrodysplasia Schmid type', 'MCDS', 'Schmid type metaphyseal dysplasia', 'Japanese type spondylometaphyseal dysplasia', 'metaphyseal chondrodysplasia, Schmid type', 'spondylometaphyseal dysplasia, Japanese type']",0080021,156500,174,,"['-0.4502', '0.11005', '0.3425', '-0.3308', '0.2502', '-0.2969', '0.12', '0.4355', '-0.3904', '-0.1342', '0.03848', '0.09705', '0.1268', '0.0703', '0.05194', '0.1434', '0.3474', '-0.0718', '-0.3062', '-0.696', '-0.1411', '-0.04282', '0.5645', '-0.02025', '-0.04532', '0.00489', '-0.01439', '-0.0988', '0.07104', '-0.07495', '0.0494', '-0.11914', '0.0529', '0.004105', '0.2708', '-0.0927', '0.08203', '-0.4517', '0.2091', '-0.1844', '0.188', '-0.3738', '0.1027', '0.1048', '0.08374', '-0.2637', '-0.1405', '0.4146', '0.10754', '-0.1454', '0.1247', '-0.2269', '0.1354', '-0.0948', '-0.32', '-0.4626', '-0.05002', '-0.386', '-0.09564', '-0.0221', '0.1997', '0.0269', '-0.298', '0.006805', '-0.2231', '-0.1012', '0.1536', '0.1248', '-0.123', '0.1467', '-0.35', '-0.1467', '0.0691', '-0.1476', '-0.057', '0.1837', '-0.1066', '-0.04855', '-0.3167', '-0.2756', '-0.12103', '0.1527', '0.07916', '0.423', '-0.2708', '0.303', '0.00847', '0.05872', '0.1608', '-0.03912', '-0.2234', '0.153', '-0.0456', '0.1586', '0.3909', '0.09094', '0.665', '-0.422', '0.288', '0.05783']",,,C537352,,,,
mondo:0007984,metaphyseal dysplasia-maxillary hypoplasia-brachydacty syndrome,"['metaphyseal dysplasia maxillary hypoplasia brachydactyly', 'metaphyseal dysplasia with maxillary hypoplasia with or without brachydactyly', 'MDMHB']",0111513,156510,2504,CN201864,"['-0.1012', '0.3691', '0.0172', '-0.1835', '0.12476', '-0.2627', '-0.1693', '0.3962', '-0.12256', '-0.397', '-0.02953', '0.02374', '-0.2644', '-0.2354', '-0.10345', '0.3787', '0.2216', '-0.1547', '-0.3625', '-0.2008', '-0.2817', '0.11884', '0.2737', '-0.357', '0.3572', '0.0525', '-0.1259', '0.02187', '0.3643', '-0.368', '0.1976', '-0.3599', '-0.04684', '-0.02324', '0.3052', '-0.2368', '-0.015076', '-0.5396', '-0.1809', '-0.4495', '0.1455', '-0.3787', '-0.0438', '-0.3806', '-0.0504', '-0.3416', '-0.2191', '0.3738', '-0.3018', '-0.4805', '0.06088', '-0.3154', '-0.00533', '0.1621', '-0.2058', '-0.7515', '-0.01855', '0.0313', '-0.1644', '0.04993', '0.1699', '-0.00816', '-0.4077', '0.113', '-0.1846', '-0.2744', '0.3281', '0.2666', '-0.3306', '0.3796', '-0.3054', '0.05676', '0.3408', '-0.0849', '-0.1497', '0.257', '-0.004288', '-0.092', '-0.1373', '-0.09045', '0.2664', '0.3367', '0.2603', '0.1641', '0.1725', '0.2053', '-0.1345', '0.651', '0.1431', '-0.00578', '-0.3125', '0.3447', '0.2617', '0.1608', '0.8193', '-0.02785', '0.2211', '-0.679', '0.2001', '0.1175']",,,,,,,
mondo:0007985,"metatarsus varus, type 1","['metatarsus varus, type I']",,156520,,C1834968,,,,C563585,,,,
mondo:0007986,metatropic dysplasia,"['Metatropic dwarfism', 'metatropic dysplasia', 'Metatropic dysplasia, nonlethal dominant']",0111514,156530,2635,,"['-0.512', '-0.1075', '-0.3306', '-0.5054', '-0.3318', '-0.5806', '0.1364', '1.125', '-1.018', '-0.8735', '0.3433', '0.369', '0.2286', '0.1921', '0.3599', '-0.1857', '0.2249', '-0.11554', '0.0788', '-0.726', '-0.03833', '0.02522', '0.6934', '-0.01294', '-0.2458', '0.2065', '-0.2451', '0.6646', '0.0796', '-0.4023', '0.1119', '-0.468', '0.1715', '0.0736', '-0.1009', '-0.4531', '0.434', '-0.744', '0.2288', '0.3357', '0.2422', '-0.006485', '0.5913', '0.3196', '-0.1266', '-0.1239', '-0.3481', '-0.2915', '0.537', '-0.005123', '-0.1946', '-0.3052', '-0.01799', '-0.1895', '-0.1499', '-0.5054', '-0.327', '-0.08014', '0.2944', '0.1611', '0.182', '0.507', '-0.45', '-0.04553', '-0.1339', '0.066', '0.227', '0.02994', '-0.1205', '0.2937', '-0.612', '0.0767', '0.1674', '0.04517', '0.2233', '0.06525', '-0.03964', '0.2098', '-0.461', '-0.145', '-0.3826', '0.3894', '0.002733', '0.5127', '-0.5586', '0.9253', '0.1233', '0.07263', '0.6', '0.07715', '-0.01913', '-0.679', '-0.287', '0.2566', '0.3452', '0.1245', '1.089', '-0.6577', '0.276', '0.4065']",C175209,,C537356,,,,
mondo:0007987,Kniest dysplasia,['Kniest dysplasia'],0080045,156550,485,C0265279,"['-0.1885', '0.005234', '-0.1194', '-0.2644', '0.3958', '-0.3472', '-0.05518', '0.3918', '-0.6143', '-0.3115', '0.2397', '-0.0628', '-0.02618', '-0.1284', '-0.3806', '0.081', '0.6846', '-0.001894', '-0.10547', '-0.5244', '-0.476', '0.14', '0.578', '-0.1105', '-0.2996', '0.2402', '-0.4365', '-0.1148', '0.434', '0.4397', '0.1661', '-0.195', '0.2617', '0.12335', '0.03305', '-0.008484', '0.04883', '-0.6606', '-0.1376', '-0.3367', '0.0699', '0.2301', '-0.1046', '0.1427', '-0.15', '-0.1144', '0.0589', '0.595', '0.5757', '-0.2524', '0.4927', '-0.1952', '0.1688', '-0.2961', '0.0253', '-0.717', '0.0373', '-0.1495', '-0.0449', '0.0939', '0.10156', '-0.1353', '-0.3706', '0.1292', '-0.1895', '-0.1503', '0.1174', '0.6343', '-0.3484', '0.543', '-0.5674', '0.11707', '0.1426', '-0.0002103', '-0.02757', '0.05478', '-0.255', '-0.07904', '-0.144', '-0.03864', '0.05457', '-0.1965', '-0.1556', '0.509', '-0.3486', '0.2783', '0.02235', '0.2192', '0.5234', '0.2605', '-0.2742', '0.3743', '0.2343', '0.1965', '0.5327', '0.2605', '0.4263', '-0.4595', '0.4875', '0.374']",C125594,,C537207,756.9,,,
mondo:0007988,autosomal dominant primary microcephaly,"['autosomal dominant microcephaly', 'microcephaly autosomal dominant', 'autosomal dominant primary microcephaly', 'microcephaly (disease), autosomal dominant', 'microcephaly with autosomal dominant inheritance', 'microcephaly, autosomal dominant']",14725,156580,2514,C4755316,"['0.1768', '0.1548', '0.3357', '-0.2961', '0.3474', '-0.129', '0.1183', '0.687', '-1.051', '-0.4185', '-0.01357', '0.1135', '0.6533', '0.7266', '0.708', '-0.2443', '0.7397', '0.5376', '-0.5405', '-1.16', '-0.2186', '-0.01472', '0.2986', '-0.2216', '0.4512', '0.2585', '0.03027', '0.1454', '0.2805', '-0.2456', '-0.1995', '-0.4893', '0.612', '0.2251', '-0.2993', '0.6587', '-0.608', '-0.05356', '0.2515', '-0.207', '0.09656', '0.389', '-0.6235', '-0.413', '0.2742', '-0.678', '0.8687', '0.1573', '0.06744', '-0.3013', '0.4197', '-0.6465', '-0.3088', '-0.509', '-0.04376', '0.2056', '-0.776', '0.5938', '-0.753', '0.2086', '0.472', '0.5024', '0.568', '0.1768', '-0.1119', '0.08167', '0.3792', '-0.2522', '-1.219', '0.2646', '-0.845', '1.224', '0.3633', '-0.8115', '0.1976', '0.3801', '0.2874', '-0.205', '-0.4194', '-0.1182', '-0.2498', '0.9014', '0.0943', '0.4934', '0.01535', '-0.1315', '0.4333', '-0.359', '0.929', '0.6665', '0.0439', '0.1622', '-0.3108', '0.1456', '0.0192', '0.522', '0.9287', '-0.5244', '0.6665', '-0.609']",,,C537323,,,,
mondo:0007989,congenital microcoria,"['congenital miosis', 'microcoria, congenital', 'Mcor', 'pinhole pupils', 'chromosome 13Q32 deletion syndrome', 'miosis, congenital']",,156600,566,,,,,C537550,,,,
mondo:0007990,multiple benign circumferential skin creases on limbs,"['Kunze-Riehm syndrome', 'congenital circumferential skin folds', 'CSCSC', 'Kunze Riehm syndrome', 'skin creases, multiple benign ring-shaped, of limbs', 'Michelin tire baby syndrome', 'circumferential skin creases, Kunze type', 'Michelin tyre baby syndrome', 'CCSF']",0112241,,2505,C0473586,"['-0.421', '0.2734', '0.1808', '-0.4597', '0.1433', '-0.2834', '0.03503', '0.3826', '-0.3066', '0.0082', '-0.1583', '0.1094', '0.153', '0.08746', '-0.2078', '0.003805', '-0.1288', '-0.4644', '-0.3362', '-0.1935', '0.11615', '0.02196', '0.2135', '0.01542', '0.03522', '-0.2612', '-0.329', '0.1508', '0.2656', '-0.05432', '0.3596', '-0.511', '0.3289', '0.362', '0.1577', '0.1853', '-0.263', '0.1268', '-0.0213', '-0.05124', '0.2388', '-0.2327', '-0.08704', '0.03513', '-0.02814', '-0.2834', '0.2377', '0.4304', '-0.2642', '0.02963', '-0.3691', '0.1376', '-0.1538', '0.2695', '-0.3992', '0.0322', '-0.0816', '-0.08154', '-0.2854', '0.3494', '-0.1996', '-0.03238', '-0.6978', '0.367', '-0.2715', '-0.0902', '0.1708', '0.575', '-0.0633', '0.5337', '-0.3103', '0.2507', '0.255', '-0.00881', '-0.2935', '-0.007965', '0.11816', '-0.2947', '-0.1675', '-0.4827', '0.3057', '-0.0448', '0.07996', '0.2411', '0.03735', '-0.1884', '-0.1305', '0.2764', '0.1026', '0.4358', '0.3975', '0.528', '0.3486', '0.04572', '0.5146', '-0.0687', '0.619', '-0.0964', '0.3118', '0.1838']",,,C537575,,,,
mondo:0007991,microcephaly-deafness-intellectual disability syndrome,"['microcephaly-deafness syndrome', 'Kawashima-Tsuji syndrome', 'Kawashima Tsuji syndrome', 'syndrome of microcephaly, deafness/malformed ears, intellectual disability and peculiar facies', 'syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies', 'microcephaly deafness syndrome']",,156620,2533,C0796062,,,,C537326,,,,
mondo:0007992,microcornea-glaucoma-absent frontal sinuses syndrome,"['hereditary microcornea, glaucoma, and absent frontal sinuses', 'microcornea, glaucoma, and absent frontal sinuses']",,156700,2536,C1834935,,,,C537552,,,,
mondo:0007993,microgastria-limb reduction defect syndrome,"['microgastria limb reduction defect', 'MLRD', 'congenital microgastria and limb reduction defects', 'microgastria-limb reduction defects association']",,156810,2538,C1834929,,,,C537554,,,,
mondo:0007994,micromelic bone dysplasia with cloverleaf skull,['micromelic bone dysplasia with cloverleaf skull'],,156830,,,,,,C536429,,,,
mondo:0007995,"microphthalmia, isolated, with cataract 1","['microphthalmia with cataract 1', 'cataract, congenital, with microphthalmia', 'congenital cataract with microphthalmia', 'microphthalmia, isolated, with cataract 1', 'MCOPCT1']",,156850,,C1834919,,,,C563582,,,,
mondo:0007996,"microphthalmia, isolated, with corectopia","['MCOPCR', 'microphthalmia, isolated, with corectopia', 'microphthalmia with myopia and corectopia', 'microphthalmia and corectopia']",,156900,,C1834918,,,,C563581,,,,
mondo:0007997,microspherophakia with hernia,['microspherophakia with hernia'],,157150,,C1834881,,,,C537468,,,,
mondo:0007998,microspherophakia-metaphyseal dysplasia syndrome,"['Verloes-Van Maldergem-de Marneffe syndrome', 'Verloes Van Maldergem Marneffe syndrome', 'microspherophakia-metaphyseal dysplasia', 'dominantly inherited bone dysplasia with severe eye involvement']",,157151,2551,C1834880,,,,C536540,,,,
mondo:0007999,holoprosencephaly 2,"['SIX3 holoprosencephaly', 'holoprosencephaly 2', 'holoprosencephaly type 2', 'holoprosencephaly caused by mutation in SIX3', 'HPE2']",0110872,157170,,C1834877,,C74995,,C563579,,,,
mondo:0008000,"migraine with or without aura, susceptibility to, 1","['migraine with or without aura, susceptibility to, 1', 'Mgau', 'migraine, susceptibility to', 'migraine with or without aura, susceptibility to, type 1', 'migraine without aura, susceptibility to', 'migraine, resistance to', 'migraine', 'Mgr1']",,157300,,,,,,,346.90,,,
mondo:0008001,"milia, multiple eruptive","['milia, multiple eruptive', 'MEM']",,157400,,C0343079,,,,C562823,,,,
mondo:0008002,mirror movements 1,"['mirror movements 1 and/Or agenesis of the corpus callosum', 'MRMV1', 'mirror movements type 1', 'mirror movements, congenital', 'familial congenital mirror movements caused by mutation in DCC', 'bimanual synergia', 'mirror movements 1', 'DCC familial congenital mirror movements']",,157600,,,,,,,,,,
mondo:0008003,autosomal dominant progressive external ophthalmoplegia,"['progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 1', 'adPEO', 'progressive external ophthalmoplegia, autosomal dominant', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 1', 'PEOA1']",,,254892,CN202062,"['-0.378', '0.288', '0.1854', '-0.2422', '-0.006496', '-0.4473', '0.292', '0.4697', '-0.516', '-0.09595', '-0.1941', '0.04526', '-0.2466', '0.1225', '0.06464', '-0.1025', '0.1906', '-0.0852', '-0.0787', '-0.4739', '-0.10126', '-0.011604', '-0.3997', '0.0804', '0.1279', '0.2426', '-0.08234', '-0.1703', '-0.01195', '-0.00845', '-0.04803', '0.2908', '0.2324', '-0.1395', '-0.1643', '-0.27', '-0.354', '-0.1455', '-0.2311', '-0.1221', '0.1035', '-0.239', '0.03055', '0.3044', '0.1259', '-0.302', '-0.1877', '0.1761', '0.01036', '0.04947', '-0.1102', '0.2864', '-0.1344', '-0.3008', '0.06107', '-0.4612', '0.511', '-0.2397', '-0.2756', '-0.2803', '0.2712', '-0.04474', '0.1682', '0.191', '-0.729', '-0.0524', '0.2437', '0.4438', '0.0543', '0.1986', '-0.316', '0.11584', '0.2554', '-0.1638', '0.4348', '0.157', '-0.1617', '0.2415', '-0.2391', '-0.141', '0.38', '-0.1914', '0.2883', '0.6133', '0.1001', '0.1553', '-0.0225', '0.2018', '0.1753', '0.507', '0.2732', '0.3855', '0.3096', '0.251', '0.712', '0.2041', '0.3447', '0.0991', '-0.0776', '0.18']",,,C563575,,,,
mondo:0008004,familial mitral valve prolapse,"['hereditary mitral valve prolapse (disease)', 'MVP', 'mitral valve prolapse, familial, autosomal dominant', 'mitral valve prolapse, familial']",,,741,,,,,,,,,
mondo:0008005,cardiospondylocarpofacial syndrome,"['cardiospondylocarpofacial syndrome', 'Forney syndrome', 'mitral regurgitation, conductive deafness, and fusion of cervical vertebrae and of carpal and tarsal bones', 'Forney Robinson Pascoe syndrome', 'congenital heart disease, deafness, and skeletal malformations', 'mitral regurgitation-deafness-skeletal anomalies syndrome', 'Forney-Robinson-Pascoe syndrome', 'CSCF']",,157800,3238,CN204053,"['-0.1521', '0.2935', '0.581', '-0.2832', '0.211', '-0.6484', '0.4397', '0.553', '-0.4304', '-0.447', '-0.02693', '-0.4783', '-0.558', '0.0393', '-0.4368', '0.3086', '0.03992', '0.10693', '-0.3672', '-0.0912', '-0.04663', '0.3015', '0.006855', '-0.261', '0.25', '0.271', '-0.00136', '0.11926', '0.5356', '-0.546', '0.5176', '-0.4458', '0.3364', '-0.2236', '0.1355', '-0.758', '-0.0898', '-0.635', '-0.3518', '-0.3767', '-0.0721', '0.2595', '0.4165', '-0.0873', '0.05884', '-0.563', '-0.05417', '0.2416', '-0.627', '0.2012', '0.0656', '-0.3677', '0.12494', '-0.3447', '-0.01976', '-0.9966', '-0.2722', '0.377', '-0.167', '0.0849', '0.1503', '-0.10425', '-0.4106', '0.1039', '-0.04166', '-0.316', '0.07465', '0.4556', '-0.4146', '0.455', '-0.669', '0.08484', '0.04376', '-0.211', '-0.291', '-0.0662', '0.07184', '0.3066', '-0.1348', '0.05624', '0.1572', '0.4597', '0.06006', '0.6484', '0.0961', '0.285', '0.2769', '0.2195', '0.0895', '-0.004307', '-0.7246', '0.4253', '0.0738', '0.306', '0.9346', '-0.0179', '0.7344', '-0.4297', '0.4473', '0.02298']",C188216,,C563572,,,,
mondo:0008006,Mobius syndrome,"['congenital facial diplegia', 'absence or underdevelopment of the 6th and 7th cranial nerves', 'congenital oculofacial paralysis', 'Moebius syndrome, Isolated cases', 'oromandibular-limb hypogenesis spectrum', 'Möbius syndrome', 'Moebius syndrome', 'Moebius sequence', 'Moebius congenital oculofacial paralysis', 'congenital facial diplegia syndrome', 'MBS', 'Mobius syndrome']",13501,157900,570,C0853240,,C84893,1001046,D020331,759.89,,10030069,
mondo:0008007,tooth ankylosis,"['calcareous tooth ankylosis (disease)', 'ankylosis of tooth', 'dental ankylosis', 'secondary retention of permanent molars', 'abnormal fusion of dental cementum with alveolar bone', 'molar I reinclusion', 'molar 1 reinclusion', 'ankylosis of teeth', 'permanent molars, secondary retention OF']",12661,157950,1077,C0155930,,,1001215,D020254,521.6,,10044019,
mondo:0008008,MOMO syndrome,"['macrocephaly-obesity-mental disability-ocular abnormalities syndrome', 'macrosomia-obesity-macrocephaly-ocular abnormalities syndrome', 'macrosomia, obesity, macrocephaly, and ocular abnormalities', 'macrosomia, obesity, macrocephaly, ocular abnormalities', 'macrocrania, obesity, ocular abnormalities (retinal coloboma and nystagmus)', 'momo syndrome']",,157980,2563,C1834759,,,,C535812,,,,
mondo:0008009,monilethrix,"['moniliform hair syndrome', 'monilethrix', 'nodose hair', 'MNLIX']",0050472,252200,573,C0546966,"['0.00857', '-0.1569', '-0.1403', '-0.205', '0.09625', '-0.4475', '0.03455', '0.2573', '-0.2369', '-0.2915', '-0.1879', '-0.2021', '0.077', '-0.0707', '-0.1656', '0.1941', '0.774', '-0.535', '-0.3022', '-0.78', '-0.3909', '-0.1445', '0.776', '-0.1365', '0.3975', '0.376', '-0.5405', '-0.2698', '-0.639', '-0.3345', '0.3396', '0.11707', '-0.1733', '0.2324', '0.69', '-0.0544', '-0.03053', '-0.2747', '0.474', '-0.3877', '0.3884', '-0.626', '0.10333', '-0.3591', '-0.10443', '-0.8335', '-0.07965', '-0.1096', '0.2432', '-0.3865', '0.00735', '-0.1342', '0.711', '0.2556', '-0.2988', '-0.4866', '0.4966', '-0.1965', '-0.1821', '-0.4753', '-0.3857', '-0.238', '-0.1249', '-0.605', '-0.02628', '0.3826', '0.3892', '0.1708', '-0.1141', '0.6', '-0.3596', '-0.355', '0.08887', '0.3784', '0.2277', '0.342', '-0.1825', '-0.8813', '0.06183', '0.1508', '0.4094', '0.2314', '0.01181', '0.198', '0.1254', '0.2401', '-0.5103', '0.112', '0.1082', '0.549', '-0.3887', '0.1787', '-0.2434', '0.4434', '0.2974', '-0.2106', '0.04214', '-0.8228', '-0.02113', '0.383']",C84894,,D056734,,,,
mondo:0008010,antigen defined by monoclonal antibody Aj9,"['antigen defined by monoclonal antibody Aj9', 'Msk1']",,158030,,,,,,,,,,
mondo:0008011,antigen defined by monoclonal antibody T87,"['antigen defined by monoclonal antibody T87', 'Msk2']",,158040,,,,,,,,,,
mondo:0008012,Monophalangy of great toe,['Monophalangy of great toe'],,158100,,C1834753,,,,C563570,,,,
mondo:0008013,chromosome 9p deletion syndrome,"['partial deletion of chromosome 9p', 'partial monosomy 9p', '9p deletion', 'partial monosomy of chromosome 9p', 'partial deletion of the short arm of chromosome 9', 'chromosome 9p deletion', 'Alfi syndrome', 'monosomy 9p syndrome', '9p- syndrome', 'partial deletion of the short arm of chromosome type 9', '9p syndrome', '9p deletion syndrome', 'deletion 9p', 'monosomy 9p', '9p monosomy', 'monosomy type 9p', 'partial monosomy of the short arm of chromosome 9']",0060732,158170,261112,,,,,C538024,758.39,,,
mondo:0008014,nondisjunction,"['mosaicism, chromosomal', 'nondisjunction', 'mixoploidy, familial']",,158250,,C1834741,,,,,,,,
mondo:0008015,motion sickness,"['travel sickness', 'motion sickness']",2951,158280,,C0026603,,,0006928,D009041,994.6,T75.3,,
mondo:0008016,trismus-pseudocamptodactyly syndrome,"['mouth, inability to open completely, and short finger-flexor tendons', 'arthrogryposis distal type 7', 'distal arthrogryposis type 7', 'Hecht syndrome', 'arthrogryposis, distal, type 7', 'trismus-pseudocamptodactyly syndrome', 'Dutch-Kentucky syndrome', 'Hecht-Beals syndrome', 'DA7']",0111603,158300,3377,C0265226,"['-0.445', '0.0645', '0.2013', '-0.1316', '-0.0359', '-0.317', '0.1095', '0.4534', '-0.459', '-0.12274', '-0.0829', '0.2195', '-0.04465', '0.1422', '-0.1098', '0.0734', '0.1565', '-0.1721', '-0.02173', '-0.284', '-0.1763', '0.1109', '0.1342', '0.003397', '0.05273', '0.0229', '-0.03552', '0.02841', '0.03357', '-0.219', '0.0336', '-0.2162', '-0.02126', '0.3213', '0.1609', '-0.2957', '-0.09937', '-0.1652', '-0.02484', '-0.2812', '-0.2659', '-0.3125', '-0.0875', '0.2437', '-0.0676', '-0.1486', '-0.0305', '0.3218', '0.1532', '0.0189', '-0.2874', '-0.05972', '0.04715', '-0.038', '-0.1907', '-0.3555', '0.0655', '-0.285', '-0.0326', '-0.05716', '0.066', '0.03918', '-0.4077', '0.1743', '-0.1938', '0.0055', '0.1257', '0.4116', '-0.1045', '0.02415', '-0.2302', '0.03766', '0.1199', '-0.09186', '0.1676', '0.1985', '-0.03024', '0.02599', '-0.11426', '-0.1857', '-0.05496', '-0.127', '0.223', '0.2788', '-0.02167', '0.2708', '-0.231', '0.2397', '0.2522', '-0.1328', '0.0492', '0.2245', '0.0756', '0.075', '0.2391', '0.02495', '0.4297', '-0.4165', '0.0395', '0.2546']",,,C535857,759.89,,,
mondo:0008017,hereditary mucoepithelial dysplasia,"['mucoepithelial dysplasia, hereditary', 'HMD', 'Urban-Schosser-Spohn syndrome']",,158310,1839,,,,,C536476,478.79,,,
mondo:0008018,Muir-Torre syndrome,"['Muir-Torre syndrome', 'MRTES', 'multiple keratoacanthoma, Muir-Torre type', 'MUIR-Torre syndrome', 'cutaneous sebaceous neoplasms and keratoacanthomas multiple with gastrointestinal and other carcinomas', 'cutaneous sebaceous neoplasms and keratoacanthomas, multiple, with gastrointestinal and Other carcinomas']",0050465,158320,587,C1321489,"['0.5083', '0.1473', '-0.4053', '-0.1866', '0.02939', '-0.2052', '0.1554', '0.2411', '-0.3364', '-0.0705', '-0.08405', '0.475', '-0.207', '-0.00765', '-0.3152', '0.01092', '0.1652', '-0.2074', '0.1273', '-0.6157', '-0.3157', '-0.1132', '0.653', '-0.3638', '0.2437', '-0.0849', '-0.3928', '-0.07227', '0.01165', '-0.5674', '0.5083', '-0.2118', '0.09607', '-0.10614', '0.1077', '0.0349', '-0.4617', '-0.05676', '-0.1476', '0.3484', '0.09064', '-0.3118', '0.327', '-0.3447', '0.427', '0.1666', '-0.2986', '0.133', '0.04657', '0.02596', '-0.1783', '0.09595', '-0.1505', '-0.0413', '-0.5884', '0.04535', '0.2223', '-0.1006', '-0.527', '-0.1211', '0.4824', '0.2603', '-0.06573', '0.1549', '0.03625', '0.2043', '0.5605', '0.573', '0.1272', '0.4434', '0.3098', '0.3638', '0.2444', '0.00865', '0.2056', '-0.1589', '-0.196', '0.1423', '-0.1879', '-0.374', '-0.4556', '0.1492', '0.1131', '0.0346', '-0.3037', '-0.4617', '0.269', '0.02501', '-0.0004604', '-0.2964', '0.04034', '0.2612', '0.3289', '-0.1991', '0.6567', '-0.0868', '0.371', '-0.3289', '-0.268', '-0.1943']",C84905,,D055653,,,10063042,
mondo:0008019,mullerian aplasia and hyperandrogenism,"['WNT4 deficiency', 'Mullerian duct failure and hyperandrogenism', 'mullerian aplasia and hyperandrogenism', 'Müllerian duct failure and hyperandrogenism', 'Müllerian aplasia and hyperandrogenism']",0111526,158330,3109,C2675014,"['-0.5977', '-0.0693', '0.0916', '-0.7373', '0.4893', '-0.1054', '-0.1532', '0.2428', '-0.577', '-0.3123', '-0.1986', '-0.3103', '-0.2339', '0.2554', '-0.3547', '-0.333', '0.4795', '0.1871', '-0.4866', '-0.7476', '0.1307', '-0.2942', '0.668', '-0.2247', '0.834', '0.237', '0.1527', '0.2312', '0.2974', '-0.2815', '0.804', '-0.304', '0.3645', '0.1583', '0.1282', '-0.4146', '0.004154', '0.1384', '-0.2297', '-0.3335', '0.4675', '-0.12305', '0.0359', '0.004818', '-0.135', '-0.7285', '0.006382', '-0.2544', '-0.01662', '0.501', '-0.2233', '0.1366', '-0.2198', '-0.1792', '-0.486', '0.0557', '0.531', '-0.509', '-0.316', '0.2081', '0.0166', '0.4028', '0.337', '0.04834', '0.0188', '0.246', '0.12054', '0.189', '-0.4326', '0.05392', '-0.3708', '0.4028', '0.01512', '0.1271', '0.10236', '-0.64', '0.2537', '0.2073', '-0.2957', '-0.1536', '0.0618', '0.4033', '0.3328', '-0.4905', '-0.3423', '-0.2576', '-0.2406', '0.1236', '0.1927', '-0.3757', '-0.0306', '0.4302', '-0.1638', '-0.4263', '0.5986', '-0.2744', '0.296', '-0.5454', '-0.04248', '0.4346']",C120376,,C567186,,,,
mondo:0008020,multiple exostoses with spastic tetraparesis,"['Hamann Zanki schimrigk syndrome', 'multiple exostoses with spastic tetraparesis', 'spasticity multiple exostoses']",,158345,,C1834724,,,,C563566,,,,
mondo:0008021,Cowden syndrome 1,"['cerebellar granule cell Hypertrophy and megalencephaly', 'CWS1', 'cerebelloparenchymal disorder 6', 'PTEN Cowden disease', 'dysplastic gangliocytoma of the cerebellum', 'Cowden syndrome type 1', 'Cowden syndrome 1', 'multiple hamartoma syndrome', 'Cowden disease caused by mutation in PTEN', 'Lhermitte-Duclos syndrome', 'Lhermitte-Duclos disease', 'CS', 'Proteus-like syndrome']",,158350,65285,CN072330,"['-0.2773', '0.0311', '0.04443', '-0.51', '-0.2776', '-0.007355', '0.02647', '0.3604', '-0.4253', '0.0401', '-0.11255', '-0.1724', '-0.04254', '-0.3035', '-0.006306', '-0.5386', '0.2917', '-0.1409', '0.1411', '-0.7354', '-0.12286', '-0.4229', '0.2477', '-0.1621', '0.2634', '-0.07465', '-0.11176', '0.3977', '0.2372', '-0.3096', '0.01656', '0.2917', '0.3523', '0.0635', '-0.2034', '0.3047', '0.0661', '-0.1721', '-0.05182', '0.09576', '-0.0332', '0.1614', '0.5703', '-0.00824', '0.4617', '-0.3044', '-0.0541', '-0.013664', '-0.076', '0.06354', '0.2118', '0.4138', '-0.1051', '-0.522', '-0.0937', '-0.00355', '0.1578', '-0.1586', '-0.2737', '0.1956', '0.0362', '0.279', '-0.04663', '0.2698', '-0.42', '-0.08545', '0.1265', '0.4036', '-0.123', '0.5605', '-0.07733', '0.2847', '0.2866', '-0.2426', '0.2598', '-0.1119', '0.2205', '0.303', '-0.5273', '-0.07935', '-0.4045', '-0.372', '0.1652', '0.633', '0.01741', '-0.0715', '0.3005', '0.0974', '0.114', '-0.1515', '-0.08887', '0.1293', '0.0781', '-0.0858', '0.7437', '0.2494', '0.4214', '0.1517', '0.5376', '0.1382']",,,,,,,
mondo:0008022,"muscle cramps, familial","['muscle cramps, familial']",,158400,,C1834708,,,,C563563,,,,
mondo:0008023,muscular atrophy-ataxia-retinitis pigmentosa-diabetes mellitus syndrome,"['muscular atrophy ataxia retinitis pigmentosa and diabetes mellitus', 'Furukawa-Takagi-Nakao syndrome', 'muscular atrophy, ataxia, retinitis pigmentosa, and diabetes mellitus']",,158500,2579,,,,,,728.2,,,
mondo:0008024,"neuronopathy, distal hereditary motor, type 7A","['Harper-Young myopathy', 'neuronopathy, distal hereditary motor, type VIIA', 'Dhmnvp', 'HMN7A', 'HMN 7A', 'neuropathy, distal hereditary motor, type 7A', 'spinal muscular atrophy, distal, with vocal cord paralysis', 'Dhmn7A', 'SLC5A7 neuronopathy, distal hereditary motor', 'neuronopathy, distal hereditary motor caused by mutation in SLC5A7']",0111201,158580,,C1834703,,,,C563562,,,,
mondo:0008025,"neuronopathy, distal hereditary motor, type 2A","['neuropathy, distal hereditary motor, type 2A', 'HMN 2A', 'Charcot-Marie-Tooth disease, spinal, 2A', 'neuronopathy, distal hereditary motor, type IIA', 'spinal muscular atrophy, distal, adult, autosomal dominant, 2A', 'HSPB8 neuronopathy, distal hereditary motor', 'HMN2A', 'neuronopathy, distal hereditary motor caused by mutation in HSPB8']",0111208,158590,,C1834692,,,,C563561,,,,
mondo:0008026,autosomal dominant childhood-onset proximal spinal muscular atrophy without contractures,"['Sma-led', 'SMALED1', 'spinal muscular atrophy, lower extremity-predominant 1, AD', 'spinal muscular atrophy, childhood, proximal, autosomal dominant', 'Kugelberg-Welander syndrome, autosomal dominant', 'spinal muscular atrophy, juvenile, proximal, autosomal dominant', 'Lower extremity-predominant autosomal dominant proximal spinal muscular atrophy without contractures', 'spinal muscular atrophy, LOWER extremity-predominant, 1, autosomal dominant']",0070351,158600,209341,C1834690,"['-0.107', '0.10913', '0.0766', '-0.1466', '0.06506', '-0.3203', '0.02863', '0.2893', '-0.3242', '-0.08887', '-0.10345', '-0.05582', '-0.1584', '0.02959', '0.1018', '-0.0651', '0.01678', '-0.1456', '-0.0932', '-0.3538', '-0.05493', '-0.1073', '0.0656', '0.03183', '0.00478', '0.02553', '0.00745', '-0.0829', '-0.1195', '-0.1432', '0.04953', '0.02339', '0.1677', '0.004284', '-0.01362', '-0.1161', '-0.04538', '-0.0435', '0.09186', '-0.2224', '-0.0352', '-0.2642', '-0.04926', '0.1067', '-0.1212', '-0.1371', '-0.06158', '0.1829', '-0.03122', '0.03026', '-0.001409', '0.004204', '0.11725', '-0.0964', '-0.0653', '-0.1774', '0.1666', '0.01025', '-0.17', '0.00811', '0.092', '0.00957', '-0.02618', '0.01917', '-0.1567', '-0.01076', '0.1855', '0.2238', '-0.0975', '0.0718', '-0.1993', '-0.01184', '0.0712', '-0.1564', '0.1779', '0.0935', '0.002945', '0.0327', '-0.07733', '-0.02293', '0.03723', '0.05844', '0.07904', '0.277', '-0.0893', '0.125', '0.0877', '0.2075', '0.11035', '0.01964', '0.0775', '0.1653', '0.04312', '0.125', '0.337', '0.0712', '0.3486', '-0.1125', '-0.001824', '0.1334']",,,C563560,,,,
mondo:0008027,"muscular atrophy, malignant neurogenic","['muscular atrophy, malignant neurogenic']",,158650,,C1834689,,,,C563559,,,,
mondo:0008028,"muscular dystrophy, Barnes type","['muscular dystrophy, Barnes type']",,158800,,C1834688,,,,C563558,,,,
mondo:0008029,Bethlem myopathy,"['benign autosomal dominant myopathy', 'Bethlem myopathy 1', 'BTHLM1', 'benign congenital muscular dystrophy', 'Bethlem myopathy type 1']",0050663,,610,C1834674,"['-0.3792', '-0.1448', '-0.1035', '0.01291', '0.5273', '-0.8306', '0.0781', '0.315', '-0.4187', '-0.3489', '0.002855', '0.07806', '-0.262', '0.2756', '0.3755', '0.4885', '0.0653', '-0.464', '-0.336', '-0.6685', '-0.1256', '-0.005104', '0.0801', '0.0998', '-0.09235', '-0.04388', '0.0794', '-0.0786', '-0.1517', '-0.01932', '0.1403', '-0.10583', '-0.004044', '0.2278', '0.12036', '-0.6313', '-0.2542', '-0.1085', '0.3596', '0.10657', '-0.01168', '-0.754', '-0.2185', '0.4023', '0.304', '-0.1277', '-0.1318', '0.4229', '0.2349', '-0.337', '-0.1836', '-0.013306', '-0.0744', '0.1307', '-0.1887', '-0.748', '0.4194', '0.0482', '-0.3364', '-0.322', '0.3623', '-0.2842', '0.0537', '-0.02696', '-0.2603', '-0.0905', '0.1761', '0.565', '-0.01497', '0.0891', '-0.614', '-0.2627', '-0.003466', '0.1967', '0.6094', '0.6396', '-0.0918', '-0.0417', '-0.0742', '-0.11127', '0.4014', '0.3237', '0.04782', '0.02827', '-0.0915', '0.6304', '0.04236', '0.4216', '-0.056', '-0.05902', '-0.02861', '-0.1852', '-0.2478', '-0.0675', '0.2471', '0.3225', '0.589', '-0.799', '0.02937', '0.1763']",C126688,,C535436,,,,
mondo:0008030,facioscapulohumeral muscular dystrophy 1,"['muscular dystrophy, facioscapulohumeral, type 1A', 'FRG1 facioscapulohumeral muscular dystrophy', 'Landouzy-Dejerine muscular dystrophy facioscapulohumeral muscular dystrophy, infantile, included', 'facioscapulohumeral muscular dystrophy type 1', 'FSHD1A', 'muscular dystrophy, facioscapulohumeral', 'facioscapulohumeral muscular dystrophy', 'FSHD', 'facioscapulohumeral muscular dystrophy caused by mutation in FRG1', 'FSHD1', 'Landouzy-Dejerine muscular dystrophy', 'facioscapulohumeral muscular dystrophy, infantile', 'facioscapulohumeral muscular dystrophy 1', 'muscular dystrophy, facioscapulohumeral, type 1', 'facioscapulohumeral muscular dystrophy 1A', 'FSHMD1A', 'facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles', 'FMD', 'facioscapulohumeral dystrophy with sensorineural hearing loss and tortuosity of retinal arterioles, included']",0111192,158900,,,,C172704,,C536391,,,,
mondo:0008031,facioscapulohumeral muscular dystrophy 2,"['Fshd2, digenic', 'facioscapulohumeral muscular dystrophy 2, digenic', 'facioscapulohumeral muscular dystrophy type 2', 'muscular dystrophy, facioscapulohumeral, type 1B', 'facioscapulohumeral muscular dystrophy 2', 'FSHD2', 'muscular dystrophy, facioscapulohumeral, type 2', 'SMCHD1 facioscapulohumeral muscular dystrophy', 'facioscapulohumeral muscular dystrophy caused by mutation in SMCHD1', 'fascioscapulohumeral muscular dystrophy 2, digenic, digenic dominant']",0111193,158901,,C1834671,,C172705,,C563557,,,,
mondo:0008034,"muscular dystrophy, pseudohypertrophic, with Internalized capillaries","['muscular dystrophy, pseudohypertrophic, with Internalized capillaries']",,159050,,C1834652,,,,C563554,,,,
mondo:0008035,"muscular hypoplasia, congenital universal, of Krabbe","['muscular hypoplasia, congenital universal, of Krabbe']",,159100,,C1834651,,,,C563553,,,,
mondo:0008036,"myasthenia, limb-girdle, autoimmune","['myasthenia, limb-girdle, autoimmune', 'myasthenia gravis, limb-girdle']",,159400,,C1834635,,,,C563552,,,,
mondo:0008037,myelinated optic nerve fibers,['myelinated optic nerve fibers'],,159500,,,,,,,,,,
mondo:0008038,ataxia-pancytopenia syndrome,"['ATXPC', 'myelocerebellar disorder', 'ataxia-pancytopenia syndrome']",,159550,2585,C1327919,"['-0.1267', '-0.318', '0.1782', '0.0849', '-0.2145', '-0.74', '0.05573', '0.007538', '-0.542', '-0.7686', '0.04617', '0.2081', '-0.323', '-0.00794', '0.3835', '-0.2722', '-0.3296', '-0.2803', '0.08484', '-0.8203', '-0.0653', '-0.3286', '0.00454', '-0.615', '0.826', '-0.446', '0.0005827', '0.1317', '-0.2367', '-0.5767', '-0.1917', '0.3916', '-0.398', '-0.12177', '0.258', '0.1836', '-0.408', '-0.03693', '0.2944', '0.1345', '0.2993', '0.439', '-0.3586', '0.4893', '0.4182', '-0.543', '0.08', '0.4421', '0.449', '-0.162', '-0.2299', '0.079', '-0.186', '-0.2015', '0.02763', '-0.7256', '0.231', '0.3809', '-0.2019', '0.3179', '-0.3794', '0.1401', '0.1328', '-0.1793', '-0.3643', '0.48', '0.4302', '0.7715', '-0.4326', '0.5415', '0.8813', '0.518', '-0.0983', '-0.6226', '0.4968', '0.0929', '0.3262', '0.3293', '0.46', '0.296', '-0.2852', '-0.7876', '0.278', '0.739', '-0.3142', '-0.5747', '0.3296', '-0.002754', '0.5415', '0.524', '0.4656', '0.236', '0.00879', '-0.0953', '0.936', '1.17', '0.3657', '0.2598', '-0.2893', '0.01591']",C176909,,C563233,,D61.0,,
mondo:0008039,tropical spastic paraparesis,"['tropical spastic paralysis', 'HTLV-1 associated myelopathy/tropical spastic paraparesis', 'TSP', 'ham/TSP', 'tropical spastic paraplegia', 'familial spastic paraparesis, HTLV-1-associated', 'Human T-lymphotropic virus type-1-associated myelopathy/tropical spastic paraparesis', 'Human T-lymphotropic virus type I-associated myelopathy/tropical spastic paraparesis', 'myelopathy, HTLV-1-associated', 'Human T-cell leukemia virus type 1 associated myelopathy/tropical spastic paraparesis', 'tropical spastic paraparesis (formerly)', 'HTLV-associated myelopathy', 'HTLV-1-associated myelopathy/tropical spastic paraparesis', 'Human T-cell leukaemia virus type 1 associated myelopathy/tropical spastic paraparesis', 'ham']",321,159580,289326,C0030481,,,0007527,D015493,323.01,,10044696,
mondo:0008040,transient myeloproliferative syndrome,"['transient myeloproliferative syndrome', 'transient myeloproliferative disease', 'transient leukemia', 'leukemia, transient', 'myeloproliferative syndrome, transient', 'transient leurkemia of Down syndrome', 'TMD', 'transient abnormal myelopoiesis', 'Mst', 'MST', 'leukemia, transient, of Down syndrome', 'transient leukaemia', 'transient myeloproliferative syndrome (disease)', 'TAM', 'Transient abnormal myelopoiesis associated with Down syndrome', 'transient myeloproliferative disorder']",0060888,159595,420611,C1834582,,C82339,,C563551,,,,0005534
mondo:0008041,"myoclonic epilepsy, Hartung type","['myoclonic epilepsy, Hartung type']",,159600,,C1834581,,,,C563550,,,,
mondo:0008043,myoclonus-cerebellar ataxia-deafness syndrome,"['myoclonus cerebellar ataxia deafness', 'myoclonus, cerebellar ataxia, and deafness']",,159800,2589,C1834579,,,,C563549,,,,
mondo:0008044,myoclonic dystonia 11,"['dystonia-11, myoclonic', 'DYT11', 'myoclonic dystonia', 'myoclonus-dystonia syndrome', 'SGCE myoclonus-dystonia syndrome', 'dystonia, alcohol-responsive', 'myoclonus, hereditary essential', 'dystonia 11, myoclonic', 'alcohol-responsive dystonia', 'myoclonic dystonia type 11']",0090034,159900,,,,,,,,,,
mondo:0008045,spinal muscular atrophy-progressive myoclonic epilepsy syndrome,"['Jankovic Rivera syndrome', 'spinal muscular atrophy with progressive myoclonic epilepsy', 'hereditary myoclonus and progressive distal muscular atrophy', 'hereditary myoclonus-progressive distal muscular atrophy syndrome', 'Jankovic-Rivera syndrome', 'myoclonus, hereditary, with progressive distal muscular atrophy', 'myoclonus hereditary progressive distal muscular atrophy', 'SMAPME']",0111527,159950,2590,C1834569,"['0.9214', '0.1917', '-0.279', '-0.12085', '-0.5786', '-0.51', '0.7095', '0.487', '-0.6636', '-0.431', '0.1884', '-0.5166', '-0.5806', '0.513', '0.066', '0.07294', '-0.2495', '-0.6055', '-0.3872', '-0.6714', '-0.247', '0.606', '0.05365', '-0.4578', '-0.296', '-0.0938', '0.00854', '-0.1981', '-0.474', '0.2666', '0.3079', '-0.7397', '0.2439', '0.2292', '0.768', '0.536', '-0.05118', '-0.01551', '-0.0745', '-0.4336', '-0.03036', '-0.4312', '-0.01423', '-0.325', '-0.4365', '-0.742', '-0.1914', '0.2354', '0.515', '0.5356', '-0.1781', '0.01714', '0.1881', '-0.563', '0.0631', '-0.2585', '-0.1594', '0.2334', '-0.06158', '0.2108', '-0.6313', '0.4446', '0.7197', '-0.3352', '-0.36', '1.446', '0.398', '0.10333', '-0.9917', '0.587', '1.071', '1.025', '-0.01274', '-0.458', '0.0328', '0.6274', '1.148', '0.3796', '-0.4985', '0.4502', '-0.05585', '0.717', '0.3494', '0.2715', '0.3237', '0.1808', '0.0543', '0.6895', '0.6797', '0.2568', '0.00853', '-0.0162', '-0.1963', '0.0956', '0.1191', '0.2185', '0.3867', '-0.437', '0.2285', '0.2747']",,,C537563,345.10,,,
mondo:0008046,autosomal dominant myoglobinuria,"['myoglobinuria, autosomal dominant']",,160010,99846,C1834567,,,,C563546,,,,
mondo:0008047,episodic ataxia type 1,"['hereditary episodic ataxia caused by mutation in KCNA1', 'hereditary paroxysmal ataxia with neuromyotonia', 'myokymia 1', 'continuous muscle fiber activity, hereditary', 'acetazolamide-responsive periodic ataxia', 'episodic ataxia/myokymia syndrome', 'EA1', 'episodic ataxia with myokymia', 'continuous muscle fiber activity', 'Isaacs-Mertens syndrome', 'episodic ataxia, type 1', 'KCNA1 hereditary episodic ataxia', 'myokymia 1 with or without hypomagnesemia', 'myokymia with periodic ataxia', 'continuous muscle fibre activity', 'ataxia, episodic, with myokymia', 'continuous muscle fibre activity, hereditary', 'paroxysmal ataxia with neuromyotonia, hereditary']",0050989,160120,972,CN042654,"['-0.4387', '-0.1714', '-0.08295', '-0.6523', '-0.2688', '-0.1863', '0.2042', '0.2335', '-0.4824', '0.08624', '-0.1935', '0.3025', '-0.1708', '-0.11945', '0.2174', '0.1635', '-0.1533', '-0.2703', '-0.2668', '-1.032', '0.255', '-0.12085', '0.2072', '0.3948', '-0.2354', '0.1414', '0.2935', '-0.6133', '-0.4966', '-0.2786', '0.1719', '0.04263', '0.194', '-0.10944', '-0.4307', '0.3586', '-0.0737', '0.09204', '0.1711', '-0.4429', '-0.1289', '-0.2668', '-0.04825', '0.4836', '0.5557', '-0.0938', '-0.10175', '0.5317', '0.273', '0.652', '-0.2445', '0.2065', '0.1178', '0.02518', '0.0633', '-0.4067', '0.5127', '-0.1294', '-0.3225', '-0.002602', '0.2744', '0.1256', '0.4192', '0.1542', '-0.3484', '0.2585', '0.336', '0.2744', '-0.591', '0.09', '-0.3872', '0.1804', '0.01793', '-0.0929', '0.5127', '0.269', '0.209', '0.2319', '0.1245', '-0.537', '0.2983', '0.0849', '0.2544', '0.0986', '-0.03915', '0.276', '-0.1567', '0.334', '0.289', '0.05682', '-0.02884', '0.07043', '0.1703', '0.432', '0.29', '0.1771', '0.0983', '-0.0764', '-0.3723', '0.10236']",,,,,,,
mondo:0008048,autosomal dominant centronuclear myopathy,"['DNM2-related centronuclear myopathy', 'CNM1', 'myopathy, centronuclear, type 1', 'myopathy, centronuclear, type 3', 'CNM3', 'myopathy, centronuclear, 1', 'AD-CNM', 'centronuclear myopathy 1', 'myopathy, centronuclear, 3', 'myotubular myopathy, autosomal dominant', 'myopathy, centronuclear, autosomal dominant', 'centronuclear myopathy, autosomal dominant', 'centronuclear myopathy, autosomal, modifier of', 'autosomal dominant centronuclear myopathy caused by mutation in MYF6']",0111223,614408,169189,C3280703,"['-0.626', '-0.394', '-0.286', '-0.07434', '0.32', '-0.609', '0.2798', '0.7715', '-0.8125', '-0.7505', '-0.1359', '-0.268', '-0.12103', '0.01862', '0.2091', '0.3071', '-0.333', '-0.67', '-0.468', '-1.149', '0.6074', '-0.02538', '0.6357', '0.2952', '0.0258', '0.284', '0.1453', '-0.06238', '-0.4568', '-0.02306', '0.7754', '0.4573', '0.0738', '-0.4927', '-0.00625', '0.0866', '-0.2974', '-0.406', '0.846', '-0.1123', '0.3127', '-0.05557', '-0.089', '0.757', '0.4644', '-0.2335', '-0.3682', '0.10956', '0.00272', '0.1144', '-0.05948', '0.2339', '-0.1056', '-0.2185', '-0.3281', '-0.3835', '0.6367', '0.454', '-0.2072', '0.06042', '0.2373', '0.1924', '-0.252', '0.1776', '-0.8057', '0.0328', '0.04263', '0.546', '-0.4768', '0.3728', '-0.3193', '-0.1514', '0.3933', '0.8047', '0.6553', '-0.2324', '0.31', '-0.1622', '0.1046', '-0.5034', '0.745', '-0.3462', '0.3923', '0.621', '-0.32', '0.7197', '-0.1271', '0.627', '-0.03497', '-0.0649', '0.2546', '-0.1903', '-0.2365', '-0.04666', '0.543', '-0.01732', '0.9053', '-0.05017', '-0.4026', '0.201']",C126689,,,,,,
mondo:0008049,"myopathy, distal, infantile-onset","['myopathy, distal, infantile-onset']",0070196,160300,,C4011725,,,,,,,,
mondo:0008050,MYH7-related skeletal myopathy,"['MYH7-related skeletal myopathy', 'Laing distal myopathy', 'Laing early-onset distal myopathy', 'myopathy, distal, type 1', 'MPD1', 'myosin storage myopathy', 'myopathy, distal, 1', 'myopathy distal, type 1', 'distal myopathy type 1', 'myopathy, distal, early-onset, autosomal dominant', 'myopathy, late distal hereditary', 'Gowers disease']",0070197,160500,59135,CN074249,"['-0.1362', '-0.09204', '-0.3542', '-0.2299', '0.2766', '-0.8096', '0.2361', '0.738', '-0.92', '0.105', '-0.1078', '0.1808', '0.02846', '0.3992', '-0.0455', '-0.06775', '-0.169', '-0.3284', '-0.1522', '-0.801', '0.02626', '0.1614', '0.4524', '0.5522', '-0.1354', '0.00434', '0.2737', '-0.0848', '-0.277', '-0.11304', '0.79', '0.0992', '0.12067', '-0.0283', '0.2032', '-0.02573', '-0.2734', '-0.0877', '-0.01625', '0.01682', '-0.521', '-0.854', '0.0787', '0.7915', '-0.1553', '0.332', '-0.3538', '0.5947', '0.1698', '0.0516', '0.0542', '0.10016', '0.1274', '-0.1904', '-0.1302', '-0.617', '0.198', '-0.02206', '0.1164', '-0.0144', '0.4026', '0.1077', '-0.04922', '0.258', '-0.594', '0.03824', '0.314', '0.5537', '-0.2544', '-0.1503', '-0.1666', '-0.2585', '0.3303', '0.03354', '0.8423', '0.3071', '-0.593', '-0.1876', '-0.4075', '-0.34', '0.4011', '-0.3396', '-0.11615', '0.003092', '-0.1852', '0.01767', '-0.2393', '0.1144', '0.1953', '-0.5034', '0.2432', '-0.2257', '0.154', '0.2278', '0.2588', '0.1677', '0.687', '-0.317', '-0.2769', '0.2211']",,,,,,,
mondo:0008051,tubular aggregate myopathy,"['TAM1', 'myopathy, tubular aggregate, 1', 'myopathy, tubular aggregate, type 1']",0080089,,2593,,"['-0.501', '-0.156', '-0.0834', '-0.1708', '-0.0707', '-0.3992', '-0.1654', '0.3408', '-0.379', '-0.3455', '-0.1444', '0.3281', '-0.367', '0.315', '0.144', '0.4832', '-0.4116', '-0.2646', '-0.32', '-0.858', '0.2042', '-0.01968', '0.09686', '0.4192', '0.1193', '-0.1482', '0.04416', '-0.3606', '-0.0643', '-0.0865', '0.3696', '-0.3735', '0.1395', '-0.3914', '-0.01924', '-0.1515', '-0.2086', '-0.02487', '0.292', '0.0824', '-0.072', '-0.3267', '-0.3232', '0.2551', '0.0654', '0.0699', '-0.3884', '0.1443', '0.1556', '0.2299', '-0.1747', '0.11163', '0.09283', '-0.035', '0.1622', '-0.6904', '0.5693', '0.1055', '-0.144', '0.1329', '0.4412', '-0.01875', '-0.3418', '-0.2627', '-0.7197', '-0.05148', '0.2595', '0.412', '-0.2688', '0.08374', '-0.3242', '-0.1061', '-0.1699', '0.1221', '0.5415', '0.4897', '-0.09503', '0.1306', '0.442', '-0.0421', '0.258', '-0.1599', '0.834', '0.2524', '0.02383', '0.5703', '-0.2338', '0.405', '0.4316', '0.0074', '0.02003', '0.3958', '-0.08777', '0.2625', '0.7227', '0.2166', '0.1218', '-0.2534', '-0.2266', '-0.2322']",,,,,,,
mondo:0008052,myopathy with storage of glycoproteins and Glycosaminoglycans,['myopathy with storage of glycoproteins and Glycosaminoglycans'],,160570,,C1834532,,,,C563542,,,,
mondo:0008053,"myopia 2, autosomal dominant","['myopia 2, autosomal dominant', 'MYP2']",,160700,,C1834531,,,,C563541,,,,
mondo:0008054,juvenile dermatomyositis,"['childhood type dermatomyositis', 'childhood dermatomyositis', 'myopathy, familial idiopathic inflammatory', 'JDM', 'juvenile myositis', 'myositis', 'myoseptum inflammation', 'juvenile dermatomyositis', 'JPM', 'juvenile DM', 'myoseptumitis']",14203,,93672,C2931785,,C27576,0000557,C538250,,,10008521,
mondo:0008055,"myotonia congenita, autosomal dominant","['myotonia Levior', 'congenital myotonia, autosomal dominant form', 'Thomsen and Becker disease', 'Thomsen disease', 'Thomsen^s disease', 'myotonia congenita, dominant', 'myotonia congenita, autosomal dominant']",0081336,160800,,,,,,,359.29,,,
mondo:0008056,myotonic dystrophy type 1,"['myotonic dystrophy 1', 'DM1', 'MD1', 'Steinert myotonic dystrophy syndrome', 'myotonic dystrophy of Steinert', 'dystrophia myotonica 1', 'Steinert disease', 'dystrophia myotonica type 1', 'Steinert syndrome', 'myotonic dystrophy caused by mutation in DMPK', 'myotonic dystrophy type 1', 'Steinert myotonic dystrophy', 'Steinert^s disease', 'dystrophia myotonica', 'DMPK myotonic dystrophy']",11722,160900,273,,"['-0.11774', '0.0734', '-0.389', '-0.3052', '0.3647', '-0.1577', '0.6924', '0.661', '-0.693', '0.2139', '-0.5586', '-0.396', '-0.7134', '0.3157', '-0.015274', '0.1553', '-0.3743', '-0.1865', '-0.5327', '-0.823', '0.06616', '0.04788', '0.0841', '-0.3198', '-0.387', '-0.4973', '0.0721', '-0.3843', '0.784', '-0.423', '0.4062', '-0.1078', '0.3855', '-0.05377', '-0.3376', '-0.1423', '-0.422', '0.1703', '0.1658', '0.4617', '-0.1052', '-0.602', '0.1632', '0.349', '0.82', '0.1278', '0.2913', '0.2395', '0.2317', '0.4543', '-0.4978', '0.5664', '-0.3538', '-0.2993', '0.4814', '-0.08655', '0.401', '-0.358', '-0.008064', '-0.3906', '0.4294', '-0.1876', '0.5874', '0.1199', '0.06726', '0.0851', '0.04724', '0.2612', '-0.58', '0.0628', '-0.04388', '-0.376', '0.1589', '0.03503', '1.22', '-0.422', '0.3438', '-0.1109', '-0.2751', '-0.4502', '0.275', '-0.1199', '-0.1813', '0.2349', '0.4868', '0.577', '0.4019', '0.3157', '0.735', '-0.1536', '0.02664', '0.09534', '0.3577', '0.129', '0.3408', '-0.262', '0.6484', '0.09784', '-0.0699', '0.03943']",C84679,,,359.21,,,
mondo:0008057,"Carney complex, type 1","['Carney syndrome', 'myxoma, spotty pigmentation, and endocrine overactivity', 'PRKAR1A Carney complex', 'Carney complex caused by mutation in PRKAR1A', 'Carney Myxoma-endocrine Complex', 'lamb syndrome', 'CNC1', 'Carney complex, type 1', 'name syndrome']",,160980,,,,,,,,,,
mondo:0008058,cylindrical spirals myopathy,['myotonic myopathy with cylindrical spirals'],0080103,160990,171886,C1834418,,,,C563535,,,,
mondo:0008059,Naegeli-Franceschetti-Jadassohn syndrome,"['Naegeli-Franceschetti-Jadassohn syndrome', 'NFJ syndrome', 'Naegeli syndrome', 'NAEGELI-Franceschetti-Jadassohn syndrome', 'reticular skin changes, dental anomalies, decreased function of sweat glands, strabismus, and optic atrophy', 'Nfj syndrome', 'NFJS', 'NAEGELI syndrome']",0111528,161000,69087,C0343111,"['0.2343', '-0.0006595', '-0.275', '0.04117', '0.3', '-0.1162', '-0.246', '0.4424', '0.4456', '-0.0717', '-0.0744', '0.3328', '-0.03833', '-0.003967', '0.03503', '0.4124', '0.5566', '-0.3772', '-0.4978', '-0.5356', '-0.2705', '-0.0837', '0.1506', '-0.1057', '0.01293', '0.0523', '-0.6357', '0.1517', '-0.0954', '-0.5005', '0.5547', '-0.2069', '-0.238', '0.494', '0.07904', '-0.1786', '-0.07214', '-0.1707', '-0.0324', '0.1505', '0.1466', '-0.10156', '0.1377', '-0.1693', '0.04465', '-0.04556', '-0.3904', '0.2253', '-0.2474', '-0.1669', '-0.409', '-0.0563', '0.5625', '0.298', '-0.4038', '0.10803', '0.8457', '-0.12494', '-0.7266', '-0.7197', '0.1521', '0.1835', '0.1497', '-0.2153', '0.1746', '0.028', '0.456', '0.747', '-0.1489', '0.2825', '-0.4624', '-0.4204', '-0.09204', '-0.2379', '0.4766', '-0.2329', '-0.2307', '0.01358', '-0.374', '-0.1622', '0.2336', '0.4436', '0.3962', '0.2231', '-0.2198', '0.1627', '-0.3704', '0.5327', '-0.01268', '0.061', '-0.095', '0.4734', '0.568', '0.4875', '0.3618', '-0.2593', '0.0322', '-0.828', '0.3005', '0.4355']",,,C538331,,,,
mondo:0008060,nonsyndromic congenital nail disorder 1,"['nonsyndromic congenital nail disorder type 1', 'FZD6 inherited isolated nail anomaly', 'claw-Shaped nails', 'NDNC10', 'autosomal recessive nail dysplasia', 'trachyonychia', 'nail disorder, nonsyndromic congenital, 10', 'nonsyndromic congenital nail disorder type 10', 'idiopathic trachyonychia', 'nail disorder, nonsyndromic congenital, 1', 'sandpaper nails', 'onychauxis, hyponychia, and onycholysis', 'twenty-nail dystrophy', 'nonsyndromic congenital nail disorder 10', 'onychodystrophy totalis', 'onychodystrophy totalis, isolated', 'autosomal dominant nail dysplasia', 'nail disorder, nonsyndromic congenital 1', 'twenty nail dystrophy', 'inherited isolated nail anomaly caused by mutation in FZD6', 'nail Growth', 'nail disorder, nonsyndromic congenital, type 10', 'NDNC1']",0080088,161050,79153,C3279974,"['-0.03345', '0.2013', '0.07587', '-0.2969', '0.5166', '-0.339', '-0.1865', '0.1757', '-0.10095', '-0.07666', '-0.1113', '0.142', '-0.2947', '-0.0726', '0.0464', '0.2922', '0.346', '-0.4702', '-0.1614', '-0.5464', '-0.3086', '-0.02403', '0.1373', '0.0345', '0.1808', '0.3757', '-0.2445', '0.0779', '0.03537', '-0.3228', '0.2717', '-0.1709', '-0.01941', '0.2832', '0.0413', '-0.0592', '-0.2043', '-0.326', '0.007053', '-0.208', '-0.1011', '-0.3135', '0.0009336', '-0.365', '-0.1576', '-0.2573', '-0.0799', '0.1423', '-0.01063', '-0.537', '0.09656', '0.04642', '0.322', '0.04767', '-0.3875', '-0.4827', '0.2357', '0.05057', '-0.542', '-0.2129', '0.1616', '-0.08234', '-0.3103', '-0.05566', '0.07184', '0.04453', '0.2096', '0.4592', '-0.01097', '0.317', '-0.51', '-0.3657', '0.3398', '-0.0888', '0.356', '0.005245', '-0.2216', '0.06604', '0.1451', '-0.2583', '-0.09973', '0.033', '-0.002596', '0.1649', '0.3003', '0.03091', '-0.0849', '0.4448', '0.1793', '0.3035', '0.03906', '0.3628', '0.1184', '0.4272', '0.5356', '0.05762', '0.4597', '-0.629', '0.1735', '0.3577']",,,C562907,703.8,,,
mondo:0008061,nail-patella syndrome,"['arthro-onychodysplasia', 'Fong disease', 'NPS1', 'NPS', 'hereditary Osteo-onychodysplasia', 'onychoosteodysplasia', 'NPS 1', 'iliac horn syndrome', 'Turner-Kieser syndrome', 'osteo-onychodysplasia', 'nail-patella syndrome', 'nail patella syndrome', 'hereditary onychoostedysplasia', 'Turner-Kiser syndrome']",9467,161200,2614,C0027341,"['-0.3503', '-0.855', '-0.0662', '-0.10516', '0.5786', '-0.1827', '-0.176', '0.807', '-0.2217', '-0.3914', '-0.3633', '-0.1312', '0.11365', '0.765', '0.6045', '0.11444', '0.084', '-0.1686', '-0.1235', '-0.8237', '-0.4543', '-0.0606', '0.533', '0.3826', '-0.07654', '-0.089', '0.2386', '-0.04306', '0.4094', '-0.1475', '0.44', '-0.425', '0.0159', '0.1833', '0.2177', '-0.53', '-0.0905', '-0.892', '0.03262', '-0.1417', '-0.1736', '-0.1344', '0.633', '-0.2534', '0.0619', '-0.8267', '-0.1832', '0.08435', '0.3645', '-0.3057', '-0.03235', '0.5605', '0.4917', '0.2048', '-0.2434', '-0.2756', '-0.2148', '-0.512', '-0.5923', '-0.3296', '0.459', '-0.316', '-0.4934', '0.11224', '-0.1029', '0.269', '0.288', '0.5044', '-0.01973', '0.00826', '0.0054', '0.05563', '-0.5176', '0.1779', '0.447', '-0.1139', '0.2433', '-0.4553', '-0.01628', '-0.3743', '0.002592', '-0.02617', '-0.1898', '0.6865', '-0.03683', '-0.1382', '-0.3452', '0.6753', '-0.4622', '0.01246', '0.3232', '-0.2052', '-0.3425', '-0.0736', '0.5737', '-0.6523', '0.5996', '-0.1606', '0.03198', '0.4626']",C75120,,D009261,759.89,,10063431,
mondo:0008062,narcolepsy 1,"['narcolepsy 1', 'narcolepsy caused by mutation in HCRT', 'NRCLP1', 'narcolepsy type 1', 'narcoleptic syndrome 1', 'HCRT narcolepsy', 'cataplexy']",,161400,,C1834372,,C84618,,C563534,,,,
mondo:0008063,"nasal alar collapse, bilateral","['nasal alar collapse, bilateral']",,161470,,C1834371,,,,C563533,,,,
mondo:0008064,"nasal bones, absence of","['nasal bones, absence of']",,161480,,C4082198,,,,C562753,,,,
mondo:0008065,"nasal groove, familial transverse","['nasal groove, familial transverse']",,161500,,C1834370,,,,,,,,
mondo:0008066,"nasal hyperpigmentation, familial transverse","['nasal hyperpigmentation, familial transverse']",,161530,,C1834369,,,,,,,,
mondo:0008067,"nasopharyngeal carcinoma, susceptibility to, 2","['nasopharyngeal carcinoma, susceptibility to, type 2', 'Npca2', 'NPCA2', 'nasopharyngeal carcinoma, susceptibility to, 2']",,161550,,C2750548,,,,,,,,
mondo:0008069,"necrotizing encephalomyelopathy, subacute, of Leigh, adult","['necrotizing encephalomyelopathy, subacute, of Leigh, adult', 'Leigh syndrome, adult']",,161700,,C1834340,,,,C563530,,,,
mondo:0008070,nemaline myopathy 3,"['ACTA1 nemaline myopathy', 'nemaline myopathy 3', 'nemaline myopathy type 3', 'NEM3', 'congenital myopathy with excess of thin filaments', 'nemaline myopathy 3, autosomal dominant or recessive', 'myopathy, actin, congenital, with cores', 'myopathy, actin, congenital, with Excess of thin myofilaments', 'nemaline myopathy 3, with intranuclear rods', 'actin myopathy', 'nemaline myopathy caused by mutation in ACTA1']",0110927,161800,98904,CN187050,"['-0.4282', '-0.01382', '-0.01758', '-0.1426', '0.02156', '-0.5176', '0.0754', '0.1669', '-0.6675', '-0.0343', '-0.3452', '-0.1522', '0.1328', '-0.2175', '-0.05365', '0.514', '-0.3657', '-0.2261', '-0.1912', '-0.644', '0.2295', '0.02206', '0.55', '0.1848', '0.265', '0.0806', '0.2676', '-0.2051', '-0.1134', '0.015114', '0.2278', '0.03195', '0.3638', '0.013306', '0.02037', '-0.04898', '-0.1277', '-0.01125', '0.01076', '-0.4563', '-0.39', '-0.5576', '-0.03967', '0.3096', '-0.159', '0.06027', '-0.1141', '-0.05594', '0.2236', '0.3872', '-0.2915', '-0.2092', '0.1577', '-0.2688', '-0.1796', '-0.5425', '0.3228', '-0.004112', '0.04346', '-0.1112', '-0.078', '0.1444', '-0.2194', '-0.04755', '-0.2052', '-0.0691', '0.3303', '0.3403', '-0.2927', '0.0857', '-0.0973', '0.04324', '0.12286', '0.414', '0.1958', '-0.1719', '0.0978', '-0.1227', '-0.2246', '-0.1217', '0.2722', '-0.1898', '0.4568', '0.38', '-0.1403', '0.2659', '0.087', '0.569', '0.5273', '-0.1724', '-0.001018', '0.2913', '0.2308', '0.3633', '0.4001', '0.289', '0.2383', '-0.0592', '0.00468', '0.1713']",C129870,,C580202,,,,
mondo:0008071,autosomal dominant progressive nephropathy with hypertension,"['nephritis, familial, without deafness or ocular defect', 'RFH1', 'renal failure, adult-onset', 'nephropathy-hypertension', 'renal failure, progressive, with hypertension', 'nephropathy, familial']",,161900,88659,C3839782,,,,C562889,583.9,,,
mondo:0008072,"IgA nephropathy, susceptibility to, 1","['berger disease', 'IGAN1', 'nephritis, IgA type', 'Igan', 'glomerulonephritis, IgA', 'IgA nephropathy, susceptibility to, 1']",,161950,,,,,,,,,,
mondo:0008073,familial juvenile hyperuricemic nephropathy type 1,"['hyperuricemic nephropathy, familial juvenile, type 1', 'medullary cystic kidney disease 2', 'medullary cystic kidney disease type II', 'UMOD-associated FJHN', 'ADTKD-UMOD', 'gouty nephropathy, familial juvenile', 'familial juvenile hyperuricaemic nephropathy', 'familial nephropathy with gout', 'UMOD-related ADTKD', 'nephropathy, familial, with gout', 'hyperuricemic nephropathy, familial juvenile, 1', 'tubulointerstitial kidney disease, autosomal dominant, 1', 'medullary cystic kidney disease 2, autosomal dominant', 'HNFJ1', 'UMOD-related autosomal dominant tubulointerstitial kidney disease', 'FJHN type 1', 'medullary cystic kidney disease type 2', 'glomerulocystic kidney disease with hyperuricemia and isosthenuria', 'hyperuricemic nephropathy, familial juvenile', 'MCKD2', 'familial juvenile gouty nephropathy', 'uromodulin-associated kidney disease', 'ADMCKD2', 'autosomal dominant tubulointerstitial kidney disease due to mutations in UMOD', 'UMOD familial juvenile hyperuricemic nephropathy', 'autosomal dominant medullary cystic kidney disease type 2', 'UMOD-related kidney disease', 'UMOD-associated familial juvenile hyperuricemic nephropathy', 'familial juvenile hyperuricemic nephropathy caused by mutation in UMOD']",,609886,88950,CN239214,"['0.03123', '0.1835', '-0.05045', '-0.04007', '0.03503', '-0.2651', '-0.0955', '0.1833', '-0.3047', '0.2222', '-0.05826', '0.0003054', '-0.1323', '0.01826', '-0.0992', '-0.3794', '0.09546', '0.0661', '0.2162', '-0.3965', '-0.05753', '-0.1786', '0.3352', '-0.23', '0.0266', '-0.0888', '0.0636', '-0.08044', '0.01834', '-0.1362', '0.2262', '0.0826', '0.3105', '0.2004', '0.04025', '-0.2732', '-0.0894', '-0.05157', '-0.07556', '-0.02557', '-0.0815', '-0.3005', '0.259', '-0.01552', '-0.1027', '-0.0863', '-0.1357', '0.2173', '0.0739', '0.065', '0.1066', '0.12463', '0.1154', '-0.2262', '-0.04776', '-0.2162', '0.1713', '-0.2257', '-0.3948', '-0.02937', '0.2488', '0.02985', '0.03137', '-0.1329', '0.1774', '-0.1089', '0.441', '0.2708', '-0.303', '0.129', '-0.1808', '-0.1512', '0.1586', '-0.1699', '0.1569', '-0.00863', '-0.12067', '0.3064', '-0.2524', '-0.01012', '-0.0732', '0.1603', '-0.1782', '0.10675', '-0.03787', '-0.11554', '0.2424', '0.02065', '0.118', '0.04556', '0.1231', '0.2593', '0.08417', '-0.05182', '0.4102', '0.04633', '0.4453', '-0.2957', '-0.2642', '0.1504']",C123172,0008618,C563693,,,,
mondo:0008075,schwannomatosis,"['Neurinomatosis', 'congenital cutaneous neurilemmomatosis', 'schwannomatosis', 'neurinoma', 'neurilemmomatosis', 'neurilemmomatosis congenital cutaneous', 'neurilemmomatosis, congenital cutaneous', 'Schwannomatosis', 'NF3']",3204,,93921,C1335929,"['0.3655', '0.5264', '0.1913', '-0.512', '0.7485', '0.03616', '-0.1664', '0.6763', '-0.87', '-0.1616', '-0.1971', '0.001047', '0.174', '0.572', '-0.1643', '0.06476', '0.3296', '0.3384', '-0.4988', '-0.00143', '-0.2517', '-0.38', '0.02766', '0.2795', '-0.3418', '-0.2314', '-0.1847', '-0.822', '0.4636', '0.2666', '0.5303', '-0.7866', '0.132', '0.0636', '-0.666', '-0.2482', '-0.63', '0.1433', '0.1425', '-0.301', '0.3286', '0.2842', '0.2043', '-0.04288', '0.5776', '0.0692', '-0.329', '0.1129', '1.244', '-0.1018', '0.314', '0.4348', '-0.11664', '-0.03708', '0.2532', '0.3093', '-0.09564', '0.292', '-0.3987', '0.0185', '-0.567', '-0.105', '-0.2375', '-0.1904', '-0.2861', '1.057', '0.3691', '0.754', '-0.4915', '0.8105', '0.501', '0.0886', '0.0811', '-0.7686', '0.6255', '-0.2544', '-0.4995', '0.9453', '0.0826', '-0.3982', '-0.10474', '0.0685', '0.4412', '0.3604', '-0.4915', '-0.7227', '0.4512', '0.523', '0.69', '0.5483', '-0.6567', '0.504', '-0.661', '-0.781', '0.6895', '-0.06113', '0.564', '-0.2659', '0.1577', '0.4478']",C6557,,,237.73,,,
mondo:0008076,amyotrophic neuralgia,"['hereditary neuralgic amyotrophy', 'amyotrophy, hereditary neuralgic', 'neuritis with brachial predilection', 'neuralgic amyotrophy', 'amyotrophy, hereditary neuralgic, with predilection for brachial plexus', 'hereditary brachial plexus neuropathy', 'brachial plexus neuropathy, hereditary', 'HNA']",10383,162100,,,,,,D020968,353.5,,,
mondo:0008078,"neurofibromatosis, familial spinal","['neurofibromatosis, familial spinal', 'Fsnf']",,162210,,C1834235,,,,C563523,,,,
mondo:0008079,neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome,"['Npdc syndrome', 'neurofibromatosis-pheochromocytoma-duodenal carcinoid syndrome', 'duodenal carcinoid syndrome']",,162240,,C1834232,,,,C563522,,,,
mondo:0008080,"neurofibromatosis, type III, mixed central and peripheral","['neurofibromas, palmar cutaneous', 'NF3A', 'neurofibromatosis, type III, Riccardi type', 'Nf 3', 'neurofibromatosis, type III, mixed central and peripheral', 'neurofibromatosis, type III, of Riccardi']",,162260,,,,,,C537389,,,,
mondo:0008081,"neurofibromatosis, type IV, of Riccardi","['neurofibromatosis, atypical', 'neurofibromatosis, variant form(S) of', 'neurofibromatosis, type IV, of Riccardi', 'NF4', 'neurofibromatosis, type IV, of RICCARDI', 'Nf 4']",,162270,,,,,,C537392,,,,
mondo:0008082,multiple endocrine neoplasia type 2B,"['mucosal neuroma syndrome', 'multiple endocrine neoplasia type 2B', 'mucosal Neuroma syndrome', 'multiple endocrine neoplasia, type 3 (formerly)', 'Neuromata, mucosal, with endocrine tumours', 'multiple endocrine neoplasia, type III, formerly', 'men type 2B', 'multiple endocrine adenomatosis type IIB', 'multiple endocrine neoplasia type III', 'multiple endocrine neoplasia, type 3', 'multiple endocrine neoplasia IIB', 'Wagenmann-Froboese syndrome', 'multiple endocrine neoplasia, type III', 'multiple endocrine neoplasia, type IIB', 'men type IIB', 'men IIB', 'multiple endocrine neoplasia type IIB', 'Neuromata, mucosal, with endocrine tumors', 'men 2B', 'MEN2B', 'multiple endocrine neoplasia type 3', 'multiple endocrine neoplasia, type 2B']",10016,162300,247709,C0025269,"['0.06903', '0.4375', '-0.2454', '-0.1719', '-0.1555', '-0.1757', '0.2783', '0.7676', '-0.6694', '-0.3413', '0.3853', '0.11774', '-0.6626', '-0.2751', '-0.4966', '-0.07043', '0.1891', '-0.3652', '-0.1754', '-0.3533', '-0.001178', '-0.4392', '0.5977', '-0.4456', '0.307', '0.4111', '-0.487', '-0.3733', '0.382', '-0.06555', '0.1132', '-0.1832', '0.3694', '0.1501', '0.0965', '-0.4163', '-0.583', '-0.05527', '-0.4348', '0.3794', '0.011086', '-0.4392', '0.333', '-0.395', '0.676', '0.328', '0.10016', '0.1862', '0.1054', '-0.0228', '-0.02058', '0.4827', '-0.03574', '-0.6226', '-0.7397', '-0.1569', '0.0394', '-0.1323', '-0.10693', '-0.10223', '0.733', '0.3152', '-0.0688', '-0.423', '0.2336', '0.047', '0.3416', '-0.1803', '-0.1938', '0.5034', '-0.03041', '-0.2842', '-0.07086', '-0.6035', '0.1243', '0.03029', '-0.3691', '0.1936', '-0.4626', '-0.4768', '-0.1301', '-0.106', '-0.312', '-0.4854', '-0.314', '0.2052', '0.2568', '-0.2964', '0.2522', '-0.1478', '0.03864', '-0.1494', '0.807', '-0.06433', '1.132', '0.1458', '-0.04675', '-0.582', '0.1492', '0.2515']",C3227,,D018814,258.03,,10056420,
mondo:0008083,"ceroid lipofuscinosis, neuronal, 4 (Kufs type)","['Kufs disease, autosomal dominant', 'Kuf^s disease type B', 'neuronal ceroid lipofuscinosis type 4B', 'adult neuronal ceroid lipofuscinosis 4B', 'CLN4B disease', 'neuronal ceroid lipofuscinosis 4B', 'autosomal dominant Kufs disease', 'neuronal ceroid lipofuscinosis 4 parry type', 'CLN4B', 'ceroid lipofuscinosis, neuronal, parry type', 'ceroid lipofuscinosis, neuronal, 4 (Kufs type), autosomal dominant', 'ceroid lipofuscinosis, neuronal, 4 (Kufs type)', 'CLN4', 'autosomal dominant neuronal ceroid lipofuscinosis 4B', 'ceroid lipofuscinosis, neuronal, 4B, autosomal dominant', 'neuronal ceroid lipofuscinosis, parry type', 'Kuf^s disease, autosomal dominant']",0110720,162350,228343,C4284284,"['-0.2214', '0.5034', '-0.2046', '0.007435', '0.2502', '-0.309', '-0.3003', '-0.176', '-0.3416', '-0.1016', '0.0894', '0.0991', '0.2188', '-0.3857', '0.04898', '-0.145', '-0.1589', '-0.1418', '0.01086', '-0.453', '0.1395', '-0.1292', '0.4673', '0.011185', '-0.004017', '-0.01142', '0.05563', '-0.0855', '0.01235', '-0.29', '0.3516', '0.1013', '0.2761', '-0.03174', '0.132', '-0.2257', '-0.0579', '-0.08386', '-0.3943', '-0.58', '-5.91e-05', '-0.4429', '0.1753', '0.1819', '-0.1366', '-0.5913', '0.03', '0.1096', '0.4648', '0.2432', '0.03253', '0.03577', '-0.257', '-0.138', '0.0742', '-0.7627', '0.4507', '0.0838', '-0.3853', '0.2129', '0.1593', '0.1707', '0.349', '0.0692', '0.1152', '0.188', '0.224', '0.04532', '-0.582', '-0.04886', '-0.2937', '-0.241', '0.1284', '0.3596', '0.3467', '0.289', '0.08386', '0.4954', '-0.3318', '0.01264', '0.2651', '-0.133', '-0.1058', '0.1136', '-0.04794', '-0.3667', '0.205', '0.465', '0.3745', '-0.1074', '0.1749', '0.1092', '-0.1913', '-0.2646', '0.562', '0.1262', '0.2057', '-0.457', '-0.1498', '0.00988']",C128116,,,,,,
mondo:0008084,"neuropathy, congenital, with arthrogryposis multiplex","['neuropathy, congenital, with arthrogryposis multiplex', 'congenital non-progressive peripheral neuropathy with arthrogryposis multiplex']",,162370,,C1834206,,,,C535714,,,,
mondo:0008086,"neuropathy, hereditary sensory and autonomic, type 1A","['HSAN1A', 'neuropathy, hereditary sensory and autonomic, type IA', 'neuropathy, hereditary sensory radicular, autosomal dominant, type 1A', 'HSAN 1A', 'neuropathy, hereditary sensory, type 1A', 'hereditary sensory and autonomic neuropathy type IA', 'hereditary sensory and autonomic neuropathy type 1 caused by mutation in SPTLC1', 'HSN 1A', 'hereditary sensory and autonomic neuropathy type 1A', 'SPTLC1 hereditary sensory and autonomic neuropathy type 1']",0070152,162400,,,,,,,,,,
mondo:0008087,hereditary neuropathy with liability to pressure palsies,"['potato-grubbing palsy', 'neuropathy, hereditary, with liability to pressure palsies', 'polyneuropathy, familial recurrent', 'familial recurrent polyneuropathy', 'heterozygous microdeletion 17p11.2p12', 'HNPP', 'Tomaculous neuropathy', 'neuropathy, recurrent, with pressure palsies', 'tulip-bulb digger^s palsy', 'hereditary neuropathy with liability to pressure palsy', 'tomaculous neuropathy', 'current pressure-sensitive neuropathy', 'hereditary liability to pressure palsies']",0060843,162500,640,,"['0.5215', '-0.0725', '-0.34', '0.298', '-0.7764', '-0.1086', '0.8237', '0.685', '-0.1957', '-0.05322', '-0.1553', '0.628', '0.2406', '0.4128', '0.4036', '0.1099', '-0.1924', '-0.3635', '0.02899', '-0.7812', '0.341', '0.078', '0.429', '0.783', '-0.2319', '0.03906', '-0.7393', '0.2722', '-0.2113', '0.2764', '0.265', '-0.2421', '0.2437', '0.2234', '-0.2966', '-0.5884', '-0.4263', '-0.6494', '0.1873', '-0.2546', '-0.733', '-0.644', '0.0906', '0.01993', '0.526', '0.4663', '-0.9644', '0.0431', '0.387', '0.8613', '-0.535', '0.1638', '-0.6123', '-0.0009704', '-0.03053', '-0.07654', '0.492', '-0.2947', '-0.2566', '0.09125', '-0.1013', '-0.5454', '0.0771', '0.09863', '-0.575', '0.401', '-0.1678', '1.445', '0.296', '0.619', '-0.1925', '0.2522', '-0.1748', '-0.1744', '0.6694', '0.5044', '0.4133', '0.38', '-0.501', '-0.747', '-0.715', '0.1124', '0.3564', '0.785', '0.355', '0.1285', '-0.2009', '0.4087', '0.1945', '0.03308', '0.3972', '-0.04825', '-0.2322', '0.187', '0.5215', '-0.03784', '0.6045', '-0.1455', '0.5713', '0.1298']",,,C536965,,,10069382,
mondo:0008088,"neuropathy, with paraprotein in serum, cerebrospinal fluid and urine","['neuropathy, with paraprotein in serum, cerebrospinal fluid and urine']",,162600,,C1834180,,,,C563516,,,,
mondo:0008089,"neutropenia, chronic familial","['neutropenia, chronic familial', 'leukopenia benign familial', 'leukopenia, benign familial', 'neutropenia chronic familial', 'chronic familial neutropenia']",,162700,,C3665676,,,,C535815,288.09,,,
mondo:0008090,cyclic hematopoiesis,"['cyclic hematopoiesis', 'cyclic neutropenia', 'periodic neutropenia', 'cyclical neutropenia', 'dysplasia, myelocytic periodic', 'neutropenia, cyclic', 'neutropenia, periodic', 'neutropenia cyclic', 'CH', 'cyclic agranulocytosis', 'CN']",5339,162800,2686,,"['-0.3203', '0.1914', '0.02966', '-0.03952', '-0.03857', '-0.2449', '0.00525', '0.03177', '-0.11395', '-0.251', '-0.10657', '0.1841', '0.01685', '0.1025', '-0.062', '0.2216', '0.0997', '0.215', '0.0899', '-0.255', '-0.10767', '0.04184', '0.2261', '-0.4763', '0.1536', '0.1785', '-0.06506', '0.2358', '-0.2081', '-0.436', '0.06204', '0.08466', '0.2137', '0.00948', '-0.2224', '0.0962', '-0.5024', '-0.522', '-0.5254', '-0.106', '-0.1033', '0.2632', '0.2366', '-0.1381', '-0.3408', '-0.3223', '-0.1569', '-0.03592', '0.128', '0.2375', '-0.0869', '-0.1925', '-0.0821', '0.06152', '-0.06366', '0.1395', '0.4216', '-0.1604', '-0.1807', '-0.1912', '0.01979', '0.4304', '-0.01839', '-0.4019', '0.1904', '-0.1221', '0.4868', '0.1656', '-0.2783', '0.3394', '-0.5503', '-0.1231', '-0.2018', '-0.3213', '0.5337', '0.1744', '0.1969', '0.1077', '0.2715', '-0.02016', '-0.2732', '-0.1487', '0.0822', '0.05618', '0.007244', '0.3367', '0.2969', '0.3286', '0.1492', '0.0652', '0.1656', '0.1957', '-0.3364', '0.03046', '0.4587', '0.4917', '0.2125', '-0.3872', '-0.1398', '-0.0735']",C3820,,C536227,288.02,,10053176,
mondo:0008092,hereditary neutrophilia,"['neutrophilia, hereditary']",0090120,162830,279943,C0543669,"['-0.4067', '0.1765', '-0.0767', '-0.2458', '0.0402', '-0.1572', '-0.03268', '0.176', '0.08057', '0.2798', '-0.1697', '0.0848', '0.1743', '-0.128', '0.2483', '0.1669', '-0.1284', '0.1326', '0.01846', '-0.5938', '0.152', '-0.2498', '0.2185', '-0.3167', '0.2532', '-0.113', '-0.1005', '-0.03424', '-0.1982', '-0.2683', '0.3125', '0.3914', '0.3557', '-0.0634', '-0.01069', '-0.176', '-0.4631', '-0.1225', '-0.007786', '-0.446', '-0.2515', '-0.1952', '0.3945', '-0.3052', '-0.3381', '-0.3323', '-0.1768', '-0.0867', '0.3286', '0.0596', '0.1448', '-0.02374', '0.234', '0.5903', '-0.1537', '-0.1427', '0.1355', '-0.18', '-0.2316', '0.1414', '0.2578', '0.2854', '0.1917', '-0.328', '0.0511', '0.1647', '0.3892', '0.514', '-0.1846', '0.6816', '-0.2405', '-0.2598', '-0.2189', '0.1464', '0.149', '-0.04517', '0.166', '0.2383', '0.1381', '-0.1209', '-0.2369', '0.07336', '0.012314', '-0.02202', '-0.4158', '-0.1602', '0.457', '0.583', '-0.244', '0.0414', '0.3296', '-0.0761', '-0.07245', '-0.11835', '0.5815', '0.4285', '0.3489', '-0.3735', '-0.12415', '-0.1251']",,,C563010,,,,
mondo:0008093,"nevus, epidermal","['nevus sebaceous or wooly hair nevus, somatic', 'Nevus, wooly hair', 'epidermal nevus, somatic', 'nevus sebaceous or woolly hair nevus, somatic', 'nonepidermolytic keratinocytic nevus', 'nevus, epidermal, somatic', 'Nevus, Keratinocytic, nonepidermolytic', 'nevus, epidermal', 'Nevus, woolly hair', 'Epidermal Nevus', 'Nevus sebaceous']",0111162,162900,,,"['-0.04227', '0.0439', '-0.001191', '-0.03125', '0.0424', '-0.06824', '-0.00875', '0.05316', '-0.06082', '-0.014206', '-0.00942', '-0.01624', '0.022', '-0.02464', '-0.0405', '-0.03357', '0.03165', '-0.05524', '-0.02353', '-0.1254', '-0.006634', '-0.02235', '0.05847', '-0.048', '0.02061', '-0.0001848', '-0.02383', '0.001126', '-0.003077', '-0.06866', '0.09344', '0.00434', '0.05844', '0.03043', '0.01988', '-0.003582', '-0.011284', '-0.004375', '-0.010475', '-0.0668', '0.02892', '-0.0707', '0.01364', '-0.0371', '-0.00928', '-0.04324', '0.004936', '0.04456', '0.01982', '0.02216', '-0.01952', '-0.011925', '-0.003944', '0.03186', '-0.073', '-0.007565', '0.061', '-0.02237', '-0.0961', '-0.01076', '0.04688', '0.02525', '-0.01706', '0.04224', '0.00731', '-0.0104', '0.06775', '0.0631', '-0.04913', '0.0977', '-0.04193', '-0.007225', '0.010796', '0.014275', '-0.003078', '0.02234', '0.01245', '0.009544', '-0.01263', '-0.0497', '-0.01458', '-0.008064', '-0.0082', '0.06073', '-0.02286', '-0.027', '0.009544', '0.067', '0.0563', '0.01787', '0.04184', '0.0411', '0.001193', '0.01892', '0.1046', '-0.002953', '0.08154', '-0.08734', '0.000944', '0.02608']",C4088,,C580062,,,,
mondo:0008094,familial multiple nevi flammei,"['port wine stain', 'Salmon patch Nevus', 'port wine type hemangioma', 'port-wine stain familial multiple', 'CMC', 'nevi flammei, familial multiple', 'port wine birthmark', 'port wine stain of the skin', 'capillary malformations, congenital', 'capillary malformations', 'port-wine stain of skin', 'Nevus flammeus', 'port wine Nevus', 'familial multiple port-wine stains', 'port-wine stain', 'port wine stain of skin', 'capillary malformations, congenital, 1, somatic, mosaic']",0111529,163000,624,CN205384,"['-0.5874', '-0.297', '0.01223', '0.1117', '0.3787', '-0.256', '-0.0639', '-0.01247', '-0.8193', '-0.1394', '0.3271', '0.508', '-0.1029', '-0.1799', '-0.108', '0.2566', '0.3247', '-0.2401', '0.3198', '-0.3271', '-0.119', '0.4058', '0.2715', '-0.3677', '0.332', '-0.002743', '0.002392', '0.3958', '0.0942', '0.1128', '0.8555', '-0.685', '0.1545', '-0.2239', '0.178', '0.5312', '-0.0519', '0.4185', '-0.0667', '-0.511', '0.335', '-0.3948', '0.0183', '-0.3413', '0.11774', '-0.2546', '-0.1799', '0.26', '0.3843', '-0.5103', '-0.1088', '-0.04364', '0.2854', '0.225', '-0.3186', '-0.0948', '0.414', '0.2286', '-0.4182', '-0.0212', '-0.0732', '-0.3071', '-0.1384', '-0.1182', '0.03067', '0.1973', '0.8696', '0.396', '-0.282', '0.6553', '-0.1521', '0.4038', '-0.1464', '0.1015', '-0.0749', '-0.05753', '-0.2344', '0.2888', '0.03516', '-0.2915', '-0.2651', '-0.006187', '0.157', '0.04825', '0.1439', '-0.9287', '0.2301', '0.3318', '0.3044', '0.1444', '-0.013435', '0.6504', '-0.001371', '-0.1364', '0.846', '-0.1492', '0.2795', '-0.2534', '0.131', '0.08215']",C3840,,,,,10067193,
mondo:0008095,nevus anemicus,"['nevus anemicus (disease)', 'Nevus anemicus', 'NEVUS anemicus', 'anemicus Nevus']",,163050,,,,C3943,,,709.09,,,0025105
mondo:0008096,nevus flammeus of nape of neck,"['Unna Nevus', 'erythema nuchae', 'nevus flammeus of nape of neck']",,163100,,,,,,C567524,,,,
mondo:0008097,linear nevus sebaceous syndrome,"['organoid Nevus', 'sebaceous nevus syndrome linear', 'Epidermal Nevus syndrome, formerly', 'SFM', 'JNP', 'linear sebaceous Nevus syndrome', 'Schimmelpenning syndrome', 'Nevus sebaceus of Jadassohn', 'Nevus sebaceus syndrome', 'Nevus sebaceous of Jadassohn', 'sebaceous Nevus syndrome, linear', 'Schimmelpenning Feuerstein Mims syndrome', 'Solomon syndrome', 'SCHIMMELPENNING-FEUERSTEIN-MIMS syndrome', 'epidermal nevus syndrome', 'organoid nevus syndrome', 'Jadassohn nevus phakomatosis', 'SFM syndrome', 'linear sebaceous Nevus', 'Jadassohn Nevus phakomatosis', 'organoid nevus phakomatosis', 'organoid Nevus phakomatosis', 'Schimmelpenning-Feuerstein-Mims syndrome, somatic mosaic', 'Sfm syndrome']",0111530,163200,2612,,"['0.0688', '0.5933', '0.08246', '-0.3535', '0.2096', '0.03714', '0.2827', '0.589', '-0.699', '-0.0698', '0.1777', '-0.4238', '-0.3218', '0.2004', '-0.26', '-0.07904', '0.517', '-1.138', '-0.4724', '-0.2122', '-0.01738', '-0.1696', '0.6606', '-0.0553', '0.00962', '-0.1409', '0.0064', '-0.124', '0.07855', '-0.1072', '0.76', '-0.3267', '0.4114', '0.2285', '0.1421', '0.1355', '0.002089', '-0.439', '0.02045', '0.0995', '0.47', '0.02638', '0.569', '0.134', '0.3667', '0.10254', '0.2465', '-0.3062', '-0.4915', '-0.3042', '-0.03986', '0.8467', '0.05136', '-0.1663', '-1.308', '0.1953', '0.2289', '0.0792', '-0.494', '0.1615', '0.02686', '-0.3142', '-0.287', '0.4604', '-0.0724', '0.1779', '0.9087', '0.5776', '-0.2568', '0.4172', '0.4197', '0.1478', '0.03094', '0.4067', '-0.07294', '0.011765', '0.1947', '-0.2937', '-0.542', '-0.7896', '-0.4111', '-0.288', '-0.4285', '0.2434', '-0.3418', '-0.729', '0.3381', '0.526', '0.245', '0.4944', '0.2454', '0.2042', '0.1038', '-0.5405', '-0.02846', '-0.3145', '0.7573', '-0.3345', '0.389', '0.0338']",C4678,,,,,,
mondo:0008098,"mesomelic dwarfism, Nievergelt type","['Nievergelt syndrome', 'mesomelic dysplasia, Nievergelt type', 'mesomelic dwarfism Nievergelt type', 'radioulnar synostosis and a typical rhomboid shape of the tibia and fibula']",,163400,2633,C0432231,,,,C536120,,,,
mondo:0008099,congenital stationary night blindness autosomal dominant 2,"['night blindness, congenital stationary, autosomal dominant type 2', 'CSNBAD2', 'night blindness, congenital stationary, autosomal dominant 2', 'congenital stationary night blindness caused by mutation in PDE6B', 'night blindness, congenital stationary, Rambusch type', 'congenital stationary night blindness autosomal dominant type 2', 'PDE6B congenital stationary night blindness', 'Rambusch type congenital stationary night blindness']",0110863,163500,,C1876182,,,,C566869,,,,
mondo:0008100,nipples inverted,"['Mammillae Invertitae', 'nipples inverted']",,163600,,,,,,,,,,
mondo:0008101,familial supernumerary nipples,"['polymastia', 'polythelia, familial', 'nipples, supernumerary', 'isolated polythelia', 'accessory nipples']",,163700,2456,,,,,,,,,
mondo:0008102,"sick sinus syndrome 2, autosomal dominant","['SSS2', 'sick sinus syndrome 2', 'HCN4 sick sinus syndrome', 'atrial fibrillation with Bradyarrhythmia', 'sick sinus syndrome 2 with or without Cardiac noncompaction and/Or ascending aorta dilation', 'sick sinus syndrome 2, autosomal dominant', 'sinus node disease, familial, autosomal dominant', 'Sss, autosomal dominant', 'sick sinus syndrome caused by mutation in HCN4', 'sinus bradycardia syndrome, familial, autosomal dominant']",,163800,,C1834144,,,,C563513,,,,
mondo:0008103,"noduli Cutanei, multiple, with urinary tract abnormalities","['noduli Cutanei, multiple, with urinary tract abnormalities']",,163850,,C1834143,,,,C563512,,,,
mondo:0008104,Noonan syndrome 1,"['Noonan syndrome', 'NS1', 'pterygium colli syndrome', 'Turner phenotype with normal karyotype', 'Noonan syndrome type 1', 'Noonan syndrome 1', 'Male Turner syndrome', 'female pseudo-Turner syndrome']",0060578,163950,,C4551602,,C75459,,,,,,
mondo:0008105,"nose, anomalous shape of","['potato Nose', 'nose, anomalous shape of']",,164000,,,,,,C538354,,,,
mondo:0008106,"nystagmus 2, congenital, autosomal dominant","['Nystagmus congenital, motor 2', 'NYSTAGMUS 2, congenital, autosomal dominant', 'Nystagmus, congenital motor, 2', 'NYS2']",0111792,164100,,,,,,C537854,,,,
mondo:0008107,"nystagmus, hereditary vertical","['nystagmus, hereditary vertical', 'congenital hereditary vertical nystagmus', 'hereditary vertical nystagmus']",,164150,,C1834078,,,,C537857,,,,
mondo:0008108,oculocerebrocutaneous syndrome,"['Delleman Oorthuys syndrome', 'orbital cyst with cerebral and focal dermal malformations', 'oculocerebrocutaneous syndrome', 'OCCS', 'Delleman syndrome', 'OCC syndrome', 'Delleman-Oorthuys syndrome', 'Leichtman-Wood-Rohn syndrome', 'oculo-cerebro-cutaneous syndrome']",,164180,1647,C0796092,,,,C538088,759.89,,,
mondo:0008109,ocular cicatricial pemphigoid,"['cicatricial pemphigoid, ocular', 'pemphigoid, ocular cicatricial', 'ocular cicatricial pemphigoid', 'OCP']",,164185,,C1282359,,C84939,0008610,,,,,
mondo:0008111,oculodentodigital dysplasia,"['oculodentodigital syndrome', 'oculo-dento-digital syndrome', 'oculodentodigital dysplasia', 'ODDD syndrome', 'Meyer-Schwickerath syndrome', 'oculo-dento-digital dysplasia', 'oculodentoosseous dysplasia', 'ODDD', 'odd syndrome']",0060291,164200,2710,,"['-0.11835', '-0.485', '0.06305', '-0.384', '0.003796', '0.01072', '-0.1261', '0.9834', '-0.1759', '-0.2057', '-0.6953', '-0.636', '-0.0621', '0.1086', '-0.1027', '0.1287', '0.4297', '-0.5957', '-0.4482', '-0.5527', '0.2113', '-0.2917', '-0.05493', '0.2161', '0.3293', '-0.713', '-0.2485', '0.4084', '0.549', '-0.1833', '0.3674', '-0.05527', '0.1406', '-0.01726', '-0.2008', '-0.1833', '0.1946', '-0.3232', '-0.1488', '-0.01758', '0.01778', '-0.3926', '0.6255', '0.05328', '0.22', '-0.11304', '0.2065', '0.3965', '-0.3677', '-0.3328', '-0.04575', '0.4963', '-0.1473', '0.1497', '-0.5796', '-0.5146', '0.2551', '-0.248', '-0.1603', '-0.07465', '0.04297', '-0.0314', '-0.0887', '0.2732', '-0.5337', '0.3325', '0.4253', '0.5537', '-0.1782', '0.2477', '-0.2505', '0.3396', '-0.1481', '-0.00517', '0.1809', '-0.1917', '0.402', '-0.576', '0.2646', '0.118', '0.3513', '-0.04486', '0.0697', '0.9697', '-0.316', '0.00381', '-0.1322', '0.2021', '0.3652', '-0.4492', '-0.2585', '0.5464', '0.2778', '0.2698', '0.6187', '-0.01007', '0.4966', '-0.04956', '0.6094', '0.3445']",,,C563160,759.89,,10063691,
mondo:0008113,Schilbach-Rott syndrome,"['hypotelorism cleft palate hypospadias', 'cleft palate, hypotelorism, and hypospadias', 'ocular hypotelorism, submucosal cleft palate, and hypospadias', 'Schilbach-Rott syndrome', 'BRSS', 'blepharofacioskeletal syndrome', 'hypotelorism-cleft palate-hypospadias syndrome']",,164220,2353,,,,,C563509,,,,
mondo:0008114,obsessive-compulsive disorder,"['obsessive-compulsive disorder, susceptibility to', 'Anancastic neurosis', 'OCD', 'obsessive-compulsive disorder', 'obsessive compulsive disorder']",10933,164230,,,"['-0.0816', '0.3594', '-0.0999', '0.8965', '-0.514', '-0.3276', '0.5996', '0.3218', '-0.186', '0.2305', '0.2075', '0.1592', '0.14', '0.5635', '-0.1969', '0.2274', '-0.6357', '0.2017', '-0.3079', '-0.9946', '-0.926', '0.6187', '-0.00238', '-0.1521', '0.699', '-0.6597', '0.0768', '-0.05417', '0.1345', '-0.699', '0.3015', '-0.3328', '0.388', '0.701', '0.1433', '0.0902', '-1.076', '-0.0316', '0.3064', '-0.758', '0.792', '-0.4966', '-0.5317', '0.0633', '0.6426', '-0.1359', '-0.4155', '-0.413', '0.3413', '1.078', '-0.2585', '0.1709', '-0.3298', '0.0299', '0.3467', '0.4875', '-0.3691', '0.3225', '-0.5', '-0.711', '-0.6865', '-0.11066', '-0.0991', '-0.146', '-0.3474', '1.092', '0.4766', '0.1353', '-0.1914', '0.501', '-0.3442', '-0.2262', '-0.72', '-0.2009', '-0.1517', '0.486', '-0.2563', '0.9893', '0.02832', '-0.03223', '0.3953', '-0.3738', '-0.2006', '0.3235', '0.354', '0.5776', '-0.2483', '0.0609', '0.5566', '0.3264', '-0.0595', '0.285', '-1.013', '0.293', '0.002779', '-0.0541', '0.1283', '-1.136', '-0.2793', '0.593']",C88411,0004242,D009771,300.3,F42,,
mondo:0008115,Feingold syndrome type 1,"['Feingold syndrome type 1', 'MMT type 1', 'digital anomalies with short palpebral fissures and atresia of esophagus or duodenum', 'microcephaly-digital anomalies-normal intelligence syndrome type 1', 'oculo-digito-esophageal-duodenal syndrome type 1', 'MODED syndrome type 1', 'Feingold syndrome caused by mutation in MYCN', 'Feingold syndrome', 'Oded syndrome', 'Mmt syndrome', 'microcephaly and digital abnormalities with normal intelligence', 'FGLDS1', 'microcephaly-oculo-digito-esophageal-duodenal syndrome syndrome type 1', 'microcephaly, mental retardation, and tracheoesophageal fistula syndrome', 'microcephaly-intellectual disability-tracheoesophageal fistula syndrome type 1', 'MYCN Feingold syndrome', 'digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum type 1', 'FS1', 'oculodigitoesophagoduodenal syndrome', 'microcephaly-oculo-digito-esophageal-duodenal syndrome', 'ODED syndrome type 1', 'Brunner-Winter syndrome type 1', 'Feingold syndrome 1', 'microcephaly, intellectual disability, and tracheoesophageal fistula syndrome', 'digital anomalies with short palpebral fissures and atresia of esophagus or duodenum type 1', 'digital anomalies with short palpebral fissures and atresia of oesophagus or duodenum']",,164280,391641,CN204984,"['0.6274', '-0.503', '0.10394', '-0.5513', '-0.4941', '0.1114', '0.8696', '0.9453', '-0.7734', '-0.574', '0.2844', '0.03047', '-0.392', '0.3374', '-0.5215', '-0.0447', '-0.1227', '-0.4421', '-0.2654', '-1.292', '0.06033', '0.09625', '0.3838', '0.0786', '0.1329', '-0.03687', '-0.7036', '0.378', '0.5703', '-0.6733', '0.3936', '-0.2698', '0.396', '-0.0846', '-0.391', '0.178', '0.1349', '-0.1738', '0.255', '0.7456', '-0.2426', '-0.206', '0.9575', '-0.3726', '0.03705', '-0.0893', '-0.1302', '0.27', '-0.1247', '0.1642', '-0.8545', '-0.4092', '-0.3232', '-0.6987', '-0.0202', '-0.1782', '-0.1477', '0.2131', '-0.3394', '0.3962', '0.2786', '0.2495', '0.04977', '0.431', '-0.62', '-0.1191', '-0.234', '-0.3296', '-0.402', '0.4658', '-0.5024', '0.158', '-0.1266', '0.05774', '0.6016', '-0.1064', '0.2844', '-0.853', '-0.3005', '-0.2006', '-0.292', '0.0915', '-0.03903', '0.3223', '-0.008995', '0.4973', '0.3071', '0.6123', '-0.2004', '-0.155', '-0.2903', '-0.0911', '0.297', '-0.1272', '0.6226', '0.1969', '0.0691', '-1.155', '0.7324', '0.367']",,,,759.89,,,
mondo:0008116,oculopharyngeal muscular dystrophy,"['OPMD', 'oculopharyngeal muscular dystrophy', 'muscular dystrophy, oculopharyngeal']",11719,164300,270,C0270952,"['-0.0382', '-0.7266', '-0.6978', '-0.4941', '0.349', '-0.9194', '0.2576', '0.7773', '-1.81', '-0.949', '0.2194', '0.6', '-0.3433', '0.769', '0.2113', '0.394', '-0.9165', '-0.909', '-0.2844', '-0.7817', '-0.1138', '0.05142', '-0.04477', '0.635', '-0.0864', '-0.476', '-0.04636', '-0.76', '0.2288', '-0.3965', '0.7544', '0.07117', '0.357', '-0.1121', '0.0812', '-0.1638', '-0.631', '0.1915', '-0.03714', '-0.382', '0.1909', '-0.2915', '0.1731', '0.2426', '-0.2194', '0.5513', '0.01968', '0.7153', '-0.1665', '-0.00974', '0.4368', '-0.3682', '0.2083', '-0.907', '0.07764', '-0.4954', '0.806', '0.7275', '-0.3567', '-0.3823', '0.2925', '-0.001878', '0.1901', '-0.1799', '-0.1084', '0.04517', '0.0876', '0.181', '0.05887', '-0.02594', '-0.0828', '0.0581', '0.1868', '-0.301', '0.9146', '0.764', '0.0886', '-0.0871', '-0.2764', '-0.08563', '0.3704', '-0.607', '-0.0008974', '0.319', '-0.13', '0.4226', '-0.2393', '-0.5854', '0.5635', '-0.2473', '-0.3232', '-0.12256', '0.6406', '0.956', '0.2341', '-0.05652', '0.1638', '-0.34', '-0.0982', '-0.006264']",C84942,,D039141,,,10052181,
mondo:0008118,odontomatosis-aortae esophagus stenosis syndrome,"['Odontomatosis (multiple odontomas) with dysphagia', 'odontoma dysphagia syndrome', 'boder syndrome', 'odontoma-dysphagia syndrome']",,164330,2724,C1834013,,,,C537740,,,,
mondo:0008119,spinocerebellar ataxia type 1,"['ATXN1 autosomal dominant cerebellar ataxia type I', 'Schut-haymaker type OPCA', 'Sca1', 'spinocerebellar ataxia type 1', 'autosomal dominant cerebellar ataxia type I caused by mutation in ATXN1', 'spinocerebellar atrophy 1', 'olivopontocerebellar atrophy 1', 'olivopontocerebellar atrophy 4', 'OPCA1', 'OPCA 4', 'OPCA4', 'OPCA 1', 'cerebelloparenchymal disorder 1', 'spinocerebellar ataxia 1', 'Menzel type OPCA']",0050954,164400,98755,C0752120,"['-0.03384', '-0.00559', '-0.12427', '0.1361', '-0.3533', '-1.073', '0.1796', '0.3516', '-0.606', '-0.9307', '0.1526', '0.3716', '-0.1849', '-0.1172', '0.614', '-0.0781', '-0.1603', '-0.6733', '0.2844', '-0.9014', '-0.12054', '-0.294', '0.04132', '-0.291', '0.5493', '-0.3232', '-0.367', '0.3572', '-0.2207', '-0.745', '0.2922', '0.4119', '-0.3025', '-0.1511', '0.337', '0.05795', '-0.084', '-0.1215', '0.04156', '0.563', '0.5894', '0.2915', '-0.541', '0.3865', '0.5786', '-0.4758', '-0.0671', '0.4119', '0.1289', '0.0488', '-0.11096', '0.0642', '-0.0707', '-0.6763', '0.215', '-0.6606', '0.5703', '0.3418', '0.07446', '0.3018', '-0.348', '0.2091', '0.1499', '-0.09216', '-0.525', '0.4678', '0.1094', '0.538', '-0.486', '0.4597', '0.605', '0.2744', '-0.1686', '-0.7295', '0.7705', '0.1091', '0.3352', '0.1361', '0.2651', '0.3328', '-0.1316', '-0.904', '0.549', '0.7876', '-0.1749', '-0.302', '0.2112', '0.1432', '0.5566', '0.273', '0.381', '0.4375', '0.07306', '-0.1107', '1.228', '0.6514', '0.4277', '0.5044', '-0.1447', '0.1628']",C129982,,,,,,
mondo:0008121,"onychogryposis, pedal, with keratosis plantaris and coarse hair","['onychogryposis, pedal, with keratosis plantaris and coarse hair']",,164680,,C1833997,,,,C563506,,,,
mondo:0008123,autosomal dominant omodysplasia,"['OMOD2', 'omodysplasia 2', 'omodysplasia, autosomal dominant']",0080845,164745,93328,,"['-0.2146', '0.2996', '0.146', '-0.1744', '0.1482', '-0.2717', '-0.01276', '0.2688', '-0.3113', '-0.2588', '-0.07965', '0.05353', '-0.0355', '-0.012726', '0.0748', '0.02815', '0.0879', '-0.0366', '-0.1727', '-0.3577', '-0.176', '0.1382', '0.3018', '-0.04916', '0.05457', '0.1802', '-0.03882', '-0.2413', '0.1026', '-0.1946', '0.05292', '0.0327', '-0.01984', '0.02829', '0.04034', '-0.05914', '-0.00435', '-0.2474', '0.0638', '-0.2084', '0.01895', '-0.471', '0.0635', '0.0166', '-0.0958', '-0.3079', '-0.1719', '0.161', '0.1573', '-0.11487', '0.1609', '-0.1667', '-0.05267', '-0.03812', '-0.1816', '-0.566', '0.1862', '-0.1796', '-0.1924', '-0.1075', '0.154', '-0.04147', '-0.04892', '0.08545', '0.0005436', '-0.1564', '0.0779', '0.1531', '-0.1649', '0.1672', '-0.335', '0.01116', '0.1621', '-0.1936', '0.1921', '0.289', '-0.1813', '0.0497', '-0.1678', '-0.1798', '-0.01643', '0.06027', '0.245', '0.3025', '-0.02559', '0.2954', '0.1078', '0.2311', '0.145', '0.1816', '-0.1313', '0.1582', '0.0266', '0.137', '0.545', '0.1741', '0.4263', '-0.4104', '-0.015', '0.2017']",,,C567664,,,,
mondo:0008124,"omphalocele, autosomal","['type - hypogastric - defect in the caudal fold', 'type - epigastric - defect in the cephalic fold', 'paraomphalocele', 'omphalocele, autosomal', 'omphalocele due to duplication of 1p31.3, isolated cases', 'chromosome 1P31 Duplication syndrome']",,164750,,C3277235,,,,,,,,
mondo:0008125,nonsyndromic congenital nail disorder 5,"['nonsyndromic congenital nail disorder type 5', 'NDNC5', 'onycholysis, partial, with scleronychia', 'nail disorder, nonsyndromic congenital, 5', 'onycholysis, hereditary distal']",0080083,164800,,C1833909,,,,C563503,,,,
mondo:0008127,ophthalmomandibulomelic dysplasia,"['Pillay syndrome', 'OMM syndrome', 'Ophthalmo-mandibulo-melic dysplasia', 'ophthalmomandibulomelic dysplasia']",,164900,2741,C1833872,,,,C563501,,,,
mondo:0008128,"ophthalmoplegia, familial static","['external ophthalmoplegia, nonprogressive, congenital hereditary', 'ophthalmoplegia, familial static']",,165000,,C1833839,,,,C563500,,,,
mondo:0008129,"ophthalmoplegia, familial total, with iris transillumination","['ophthalmoplegia, familial total, with iris transillumination']",,165098,,C1833836,,,,C563499,,,,
mondo:0008130,ophthalmoplegia-intellectual disability-lingua scrotalis syndrome,"['Levic Stefanovic Nikolic syndrome', 'ophthalmoplegia, progressive, with scrotal tongue and mental deficiency', 'ophthalmoplegia-intellectual disability-lingua scrotalis syndrome', 'Levic-Stefanovic-Nikolic syndrome']",,165150,2743,C1833835,,,,C563498,,,,
mondo:0008131,"optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant","['optic atrophy, hearing loss, and peripheral neuropathy, autosomal dominant']",,165199,,C1833831,,,,C563497,,,,
mondo:0008132,optic atrophy with demyelinating disease of CNS,['optic atrophy with demyelinating disease of CNS'],0111756,165200,,C1833830,,,,C563496,,,,
mondo:0008133,optic atrophy 3,"['optic atrophy, cataract, and neurologic disorder', 'OPA3, autosomal dominant', 'autosomal dominant optic atrophy type 3', 'OPA3', 'optic atrophy 3, autosomal dominant', 'optic atrophy 3 with cataract', 'optic atrophy and cataract, autosomal dominant', 'optic atrophy 3']",0111433,165300,67036,C1833809,"['-0.354', '0.2048', '-0.05722', '-0.209', '-0.0724', '0.03394', '0.11664', '-0.000736', '-0.4185', '-0.1186', '-0.0719', '-0.3657', '-0.3867', '-0.09985', '-0.0754', '-0.4448', '-0.1451', '-0.2058', '0.1527', '-0.4863', '0.274', '-0.348', '-0.0482', '0.2896', '0.385', '0.3875', '-0.2825', '0.2103', '-0.289', '0.00601', '0.1644', '0.074', '0.549', '0.131', '-0.1203', '-0.089', '-0.11884', '-0.4312', '0.1274', '-0.2983', '0.1278', '-0.137', '0.0593', '0.01437', '0.084', '-0.1298', '0.3518', '-0.1194', '0.498', '0.079', '0.332', '0.2551', '-0.2355', '-0.6133', '0.414', '-0.1746', '0.965', '0.10565', '-0.519', '0.03784', '-0.3142', '-0.006363', '-0.01854', '0.05386', '-0.5435', '0.1879', '0.2861', '0.7935', '-0.16', '0.4766', '-0.3083', '-0.02554', '0.41', '-0.4758', '0.05786', '-0.04062', '0.4429', '0.3943', '0.02507', '-0.2715', '0.08154', '-0.1665', '0.08185', '0.4912', '-0.1735', '-0.10406', '0.3167', '0.206', '0.1964', '0.3313', '0.157', '0.1185', '0.09766', '0.0915', '0.6753', '0.11725', '0.4937', '0.443', '-0.06003', '0.2052']",,,C537128,,,,
mondo:0008134,"autosomal dominant optic atrophy, classic form","['optic atrophy, juvenile', 'optic atrophy 1', 'optic atrophy, Kjer type', 'Kjer-type optic atrophy', 'OAK', 'Kjer optic atrophy', 'optic atrophy type 1', 'OPA1', 'autosomal dominant optic atrophy, Kjer type']",0111441,165500,98673,CN207069,"['-0.6323', '-0.1262', '-0.1924', '0.1005', '0.382', '-0.529', '-0.209', '0.7627', '-0.1261', '-0.544', '-0.0634', '0.0383', '-0.09296', '0.3984', '0.2151', '-0.6', '-0.2003', '0.04108', '-0.12244', '-0.1455', '-0.677', '-0.325', '-0.1129', '0.4348', '0.05637', '-0.174', '-0.4006', '-0.001058', '0.1641', '-0.1588', '0.3347', '0.03528', '0.2412', '0.3596', '-0.1619', '-0.779', '0.04083', '-0.54', '-0.083', '0.09485', '0.2876', '-0.339', '0.31', '-0.03024', '-0.08624', '-0.3274', '-0.2201', '-0.6973', '0.4763', '0.36', '0.3591', '0.183', '-0.286', '-0.7686', '0.3591', '-0.1901', '1.53', '-0.2996', '-0.612', '0.698', '-0.3125', '-0.06885', '0.3892', '0.508', '-0.5317', '0.1498', '0.1462', '0.6323', '0.4297', '0.953', '-0.2976', '0.1335', '-0.00947', '-0.4326', '0.742', '0.248', '0.7163', '-0.1725', '-0.2761', '0.155', '0.4607', '-0.472', '0.2522', '0.948', '0.2253', '-0.17', '0.1169', '-0.1865', '-0.0827', '0.010254', '0.484', '0.1447', '0.52', '-0.371', '0.3972', '-0.03867', '0.519', '-0.4824', '-0.4336', '-0.2231']",,,,,,,
mondo:0008135,optic atrophy 13 with retinal and foveal abnormalities,"['optic atrophy with negative Electroretinograms', 'optic atrophy 13 with retinal and foveal abnormalities']",,165510,,C1833799,,,,C563494,,,,
mondo:0008136,isolated optic nerve hypoplasia,"['optic nerve hypoplasia', 'optic nerve hypoplasia, bilateral', 'isolated optic nerve hypoplasia/aplasia', 'familial bilateral optic nerve hypoplasia', 'optic nerve aplasia, bilateral', 'optic nerve hypoplasia, familial bilateral']",0111531,165550,137902,C4510723,"['-0.3616', '-0.0426', '0.1293', '-0.166', '0.1891', '0.2375', '0.2375', '0.1349', '-0.3787', '-0.05313', '-0.0923', '-0.3254', '-0.2018', '-0.03256', '-0.168', '-0.4194', '0.3123', '-0.0552', '-0.2224', '-0.5884', '0.04453', '0.05618', '0.2603', '0.1304', '0.00791', '-0.2522', '-0.2437', '0.2263', '0.1482', '0.0928', '0.4683', '0.003317', '0.35', '0.1544', '-0.1404', '0.05923', '0.05234', '-0.1675', '-0.1126', '-0.364', '0.01826', '0.04773', '0.04987', '-0.1782', '-0.1489', '-0.1946', '0.09644', '-0.1191', '0.2198', '0.23', '0.1344', '0.358', '0.0871', '-0.4014', '-0.1624', '0.0863', '0.2578', '-0.02675', '-0.364', '0.3035', '-0.1232', '-0.2588', '0.202', '0.4075', '-0.518', '0.1566', '0.1904', '0.772', '-0.3977', '0.4514', '-0.256', '0.3608', '0.11365', '0.02994', '0.08746', '-0.3855', '0.291', '0.3914', '-0.2253', '-0.4897', '-0.1663', '-0.3545', '0.3186', '0.761', '-0.2698', '-0.594', '-0.08246', '0.1575', '0.0423', '-0.01491', '0.05106', '0.5664', '0.02377', '0.1892', '0.7188', '0.05212', '0.281', '-0.295', '0.2065', '0.544']",,,,,,,
mondo:0008137,orofaciodigital syndrome X,"['OFD10', 'orofaciodigital syndrome with fibular aplasia', 'OFD syndrome 10', 'orofaciodigital syndrome type 10', 'oral-Facial-digital syndrome with fibular aplasia', 'oral facial digital syndrome type 10', 'oral-Facial-digital syndrome, type 10', 'orofaciodigital syndrome type Figuera', 'oral-facial-digital syndrome 10', 'orofaciodigital syndrome X', 'Ofds 10', 'orofaciodigital syndrome 10', 'orofaciodigital syndrome type X', 'oral facial digital syndrome 10', 'oral-facial-digital syndrome type 10', 'Figuera syndrome']",0060380,165590,2756,C1833796,,,,C563491,,,,
mondo:0008138,syndromic orbital border hypoplasia,"['Urrets-Zavalia syndrome', 'orbital margin, hypoplasia OF']",,165600,98606,C4273912,,,,C563490,,,,
mondo:0008139,OSLAM syndrome,"['osteosarcoma, limb anomalies, and erythroid macrocytosis with megaloblastic marrow', 'osteosarcoma-limb anomalies-erythroid macrocytosis syndrome', 'OSLAM syndrome', 'osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anemia', 'osteosarcoma, limb anomalies, and macrocytosis', 'osteosarcoma, limb anomalies (clinodactyly, absence of digital ray in foot, bilateral radioulnar synostosis) and macrocytosis without anaemia']",,165660,2760,C1833792,,,,C537138,,,,
mondo:0008140,ossified ear cartilages,['ossified ear cartilages'],,165670,,C1833791,,,,C563488,,,,
mondo:0008141,"ossicular malformations, familial","['familial ossicular malformations', 'ossicular malformations, familial', 'familial middle ear ossicular anomalies']",,165680,,C1833790,,,,C537142,,,,
mondo:0008142,"Thiemann disease, familial form","['aseptic necrosis of phalangeal epiphyses', 'Thiemann epiphyseal disease', 'Osteochondrosis of phalangeal epiphyses', 'osteochondritis of phalangeal epiphyses', 'osteoarthropathy of fingers, familial', 'Thiemann^s disease', 'THIEMANN disease', 'osteoarthropathy of fingers familial']",,165700,3314,C0264081,,,,C537144,716.84,,,
mondo:0008143,osteoarthritis susceptibility 1,"['osteoarthritis of hip, female-specific, susceptibility to', 'osteoarthritis susceptibility type 1', 'FRZB osteoarthritis', 'Oa', 'osteoarthritis caused by mutation in FRZB', 'osteoarthrosis', 'osteoarthritis susceptibility 1', 'OS1']",,165720,,C0029408,,,,,715.98,,,
mondo:0008145,Ollier disease,"['enchondromatosis, multiple, Ollier type', 'Ollier^s disease', 'Kast^s syndrome', 'enchondromatosis, multiple', 'Ollier type enchondromatosis', 'enchondromatosis with haemangiomata', 'multiple enchondromatosis', 'multiple cartilaginous enchondroses', 'dyschondroplasia', 'osteochondromatosis', 'Ollier disease', 'enchondromatosis']",4624,166000,296,CN203308,,C3213,,,,,10014642,
mondo:0008146,osteogenesis imperfecta type 1,"['OI1', 'osteogenesis imperfecta, type I', 'non-deforming osteogenesis imperfecta', 'osteogenesis imperfecta with blue sclerae', 'OI, type 1', 'OI type 1', 'osteogenesis imperfecta, type 1', 'osteogenesis imperfecta type I', 'classic non-deforming OI with blue sclerae', 'osteogenesis imperfecta tarda', 'Van der Hoeve syndrome', 'mild osteogenesis imperfecta', 'Adair-Dighton syndrome']",0110334,166200,216796,CN536249,"['-0.2705', '-0.012886', '0.3372', '-0.327', '0.7026', '-0.1868', '-0.151', '0.713', '-0.3315', '-0.00213', '-0.0677', '0.3076', '0.1534', '-0.2311', '-0.074', '0.003036', '0.6284', '-0.1642', '0.0988', '-0.3735', '0.1948', '0.01015', '0.8896', '0.07623', '0.0207', '0.1893', '-0.05542', '-0.289', '-0.141', '0.0861', '-0.0713', '-0.02922', '0.08905', '0.1644', '-0.2155', '-0.3564', '-0.3696', '-0.4702', '-0.3315', '-0.6626', '0.147', '-0.3367', '0.203', '-0.2788', '-0.4832', '-0.6216', '0.1672', '0.4534', '0.5435', '-0.1222', '0.376', '-0.3948', '0.4502', '-0.0801', '-0.11084', '-0.544', '-0.2625', '-0.2095', '-0.0484', '0.1931', '0.3086', '0.02115', '-0.1924', '-0.3777', '-0.2642', '0.0994', '-0.0174', '0.578', '-0.4421', '0.2024', '0.02757', '-0.2252', '0.0668', '-0.509', '0.2238', '0.02919', '-0.4465', '0.11', '0.1602', '-0.3167', '-0.1316', '-0.521', '0.05353', '0.301', '-0.4668', '0.4224', '0.10614', '0.0732', '0.5845', '-0.1222', '-0.2179', '0.4258', '-0.003494', '0.132', '0.605', '0.4949', '0.4907', '-0.4866', '-0.000807', '-0.07086']",C99003,,,,,,
mondo:0008147,osteogenesis imperfecta type 2,"['OI type 2', 'OI, type 2', 'osteogenesis imperfecta, type II', 'osteogenesis imperfecta congenita, perinatal lethal form', 'osteogenesis imperfecta congenita perinatal lethal form', 'Perinatally lethal OI', 'perinatal lethal osteogenesis imperfecta congenita', 'Vrolik type of osteogenesis imperfecta', 'osteogenesis imperfecta congenita', 'OI2', 'lethal osteogenesis imperfecta', 'osteogenesis imperfecta, type 2', 'osteogenesis imperfecta type II']",0110341,166210,216804,CN536250,,C99001,,C536042,,,,
mondo:0008148,osteogenesis imperfecta type 4,"['osteogenesis imperfecta, type 4', 'osteogenesis imperfecta with normal sclera', 'OI type 4', 'osteogenesis imperfecta with normal sclerae', 'OI type IV', 'common variable OI with normal sclerae', 'osteogenesis imperfecta type IV', 'osteogenesis imperfecta, type IV', 'OI, type 4', 'OI4']",0110340,166220,216820,C0268363,,C98576,,C536045,,,,
mondo:0008149,"osteogenesis imperfecta with opalescent teeth, blue sclerae and wormian bones but without fractures","['osteogenesis imperfecta with opalescent teeth, blue sclerae and WORMIAN bones, but without fractures']",0110335,166230,,C1833748,,,,C563487,,,,
mondo:0008150,osteoglophonic dwarfism,"['OSTEOGLOPHONIC dysplasia', 'Fairbank-Keats syndrome', 'osteoglophonic dwarfism', 'Osteoglosphonic dysplasia', 'OGD']",0111532,166250,2645,,"['-0.255', '0.1387', '-0.0713', '-0.2085', '0.4778', '-0.1483', '0.00868', '1.252', '-1.084', '-0.866', '0.3396', '-0.3557', '0.226', '0.603', '-0.275', '-0.364', '0.4849', '0.1852', '-0.5693', '-0.9805', '-1.35', '0.2715', '1.274', '-0.1377', '0.0787', '-0.3728', '-0.584', '-0.2238', '0.4375', '-0.1714', '-0.051', '-0.4753', '-0.0929', '-0.0845', '-0.3281', '-0.4312', '-0.03094', '0.26', '0.4343', '-0.1965', '0.06586', '0.5503', '-0.596', '-0.408', '0.6016', '0.0128', '-0.05383', '0.11914', '0.698', '-0.1116', '-0.164', '-0.06107', '-0.7153', '0.415', '-0.06494', '-0.7803', '-0.729', '-0.0734', '0.867', '0.3152', '-0.1617', '0.3572', '-0.209', '0.3787', '0.1968', '1.001', '-0.01172', '0.4514', '-0.373', '0.3218', '-0.3064', '0.03378', '0.0951', '-1.071', '-0.4', '0.3457', '-0.06464', '0.685', '-0.3672', '-0.02144', '-0.2712', '0.10596', '-0.1837', '0.2207', '0.3635', '-0.262', '0.2512', '-0.2255', '0.7812', '0.7104', '-0.347', '0.1155', '-0.61', '-0.4521', '0.572', '0.0796', '0.421', '-0.1343', '0.8696', '0.09863']",,,C536050,,,,
mondo:0008151,gnathodiaphyseal dysplasia,"['GNATHODIAPHYSEAL dysplasia', 'Gnathodiaphyseal sclerosis', 'Levin syndrome 2', 'osteogenesis imperfecta Levin type', 'GDD', 'gnathodiaphyseal dysplasia', 'osteogenesis imperfecta with unusual skeletal lesions']",0111533,166260,53697,C1833736,"['-0.00448', '0.2404', '0.178', '-0.3687', '-0.0249', '-0.3518', '-0.02051', '0.859', '-0.237', '-0.2861', '-0.00649', '0.3342', '-0.0767', '-0.2269', '0.3176', '0.2683', '0.2917', '-0.01332', '-0.00537', '-0.4185', '-0.0996', '-0.3164', '0.512', '-0.1522', '0.05978', '0.302', '0.0841', '-0.04715', '-0.1421', '-0.05515', '-0.09155', '-0.4324', '-0.01215', '0.2068', '0.1998', '-0.1215', '-0.1565', '-0.416', '-0.1909', '-0.4878', '-0.0442', '-0.4028', '0.2844', '-0.4663', '-0.0807', '-0.505', '-0.3723', '0.4592', '0.1827', '0.11505', '0.4292', '-0.01068', '0.4307', '-0.0862', '-0.3555', '-0.8735', '0.1366', '0.154', '-0.1065', '-0.3096', '0.5117', '0.2852', '-0.3457', '-0.4883', '0.0959', '-0.02776', '0.372', '0.2142', '-0.02779', '0.4727', '0.1973', '-0.3147', '0.206', '-0.361', '0.1493', '-0.04248', '-0.216', '0.1274', '0.1145', '-0.2136', '-0.3225', '0.2932', '0.1729', '0.301', '-0.4106', '0.1405', '-0.03174', '0.3645', '-0.02019', '-0.102', '-0.2893', '0.1036', '0.135', '0.07666', '0.6465', '0.286', '0.5854', '-0.3594', '0.10785', '-0.2161']",,,C536039,,,,
mondo:0008152,multicentric carpo-tarsal osteolysis with or without nephropathy,"['MCTO', 'multicentric carpo-tarsal osteolysis with or without nephropathy', 'idiopathic multicentric osteolysis with or without nephropathy', 'osteolysis, hereditary, of carpal bones with or without nephropathy', 'multicentric osteolysis, autosomal dominant', 'multicentric osteolysis nephropathy', 'multicentric carpotarsal osteolysis syndrome', 'Carnevale canun Mendoza syndrome']",0111534,166300,2774,C2674705,"['-0.202', '-0.2476', '0.2407', '-0.1715', '0.2328', '-0.3528', '-0.0172', '0.5522', '-0.3982', '0.02248', '-0.0602', '-0.11456', '-0.07544', '0.1154', '-0.1444', '-0.4048', '0.2246', '0.081', '-0.101', '-0.5137', '0.1907', '0.04965', '0.294', '-0.2842', '0.602', '0.1307', '-0.1282', '-0.1306', '0.2053', '0.3506', '0.1953', '-0.3767', '0.1218', '0.1345', '0.2327', '-0.44', '-0.2485', '-0.4536', '-0.1404', '0.0219', '-0.2157', '-0.2443', '0.2668', '-0.1073', '0.1895', '-0.414', '-0.2115', '0.07', '0.2225', '0.01372', '-0.05124', '0.5845', '0.2551', '0.0998', '-0.0367', '-0.2595', '-0.2034', '-0.1898', '-0.268', '0.3083', '0.4177', '-0.03253', '0.0489', '-0.2927', '-0.1627', '-0.04343', '-0.1058', '0.686', '-0.1504', '0.6035', '-0.2969', '-0.2456', '0.1534', '0.04053', '-0.03995', '-0.04907', '0.3418', '0.4905', '-0.2346', '-0.1738', '-0.1211', '-0.03857', '0.04587', '0.2413', '-0.2668', '-0.2249', '0.1604', '0.546', '0.2094', '0.4888', '0.04987', '0.1766', '-0.1884', '-0.143', '0.1682', '0.05914', '0.562', '-0.4854', '0.3647', '0.2925']",,,C567171,,,,
mondo:0008153,progressive osseous heteroplasia,"['ectopic ossification familial type', 'osseous heteroplasia, progressive', 'osteoma cutis', 'familial ectopic ossification', 'ectopic ossification, familial', 'poh']",0111535,166350,2762,C0334041,"['-0.1973', '0.223', '0.446', '-0.0669', '-0.145', '-0.872', '-0.2233', '-0.01404', '-0.262', '0.1276', '-0.2559', '-0.258', '0.2532', '-0.05984', '-0.2659', '0.0714', '-0.05862', '-0.608', '-0.2129', '-0.987', '0.3384', '0.3174', '0.9097', '0.438', '0.2268', '0.6216', '-0.05432', '-0.3052', '-0.2698', '-0.9717', '0.1907', '0.2927', '0.03262', '0.7983', '-0.1526', '-0.3364', '-0.3123', '0.494', '-0.3848', '-0.5576', '0.7363', '-0.5425', '0.3276', '0.1134', '0.853', '-0.395', '0.1483', '0.4233', '0.616', '0.00551', '0.1692', '0.02252', '0.638', '0.5273', '-0.5757', '-0.642', '0.5483', '0.33', '-0.1487', '0.2727', '0.5635', '0.013695', '-0.02313', '-0.0394', '-0.3604', '-0.1658', '0.2598', '1.014', '0.000846', '0.567', '0.255', '-0.4343', '0.321', '-0.187', '0.4539', '0.3516', '-0.3792', '0.6216', '-0.268', '-0.263', '0.4543', '-0.4434', '-0.2278', '0.1051', '-1.15', '-0.06088', '0.253', '0.08923', '-0.2122', '-0.3848', '0.2815', '-0.3044', '-0.19', '0.2864', '0.0291', '-0.0835', '0.864', '-0.1256', '0.01122', '0.4985']",,,C562735,,,10048902,
mondo:0008154,osteomas of mandible,['osteomas of mandible'],,166400,,C1833733,,,,C563485,,,,
mondo:0008155,osteomesopyknosis,"['axial osteosclerosis', 'osteomesopyknosis']",,166450,2777,C0432264,,,,C537792,,,,
mondo:0008156,autosomal dominant osteopetrosis 2,"['Albers-Schonberg osteopetrosis', 'OPTA2', 'osteopetrosis, autosomal dominant type 2', 'autosomal dominant Albers-Schonberg disease', 'osteopetrosis autosomal dominant type 2', 'osteosclerosis Fragilis generalisata', 'marble bones, autosomal dominant', 'Albers-Schönberg osteopetrosis', 'autosomal dominant osteopetrosis type II', 'osteopetrosis, autosomal dominant 2', 'osteopetrosis, autosomal dominant, type 2', 'Albers-Schonberg disease, autosomal dominant', 'autosomal dominant osteopetrosis type 2']",0110938,166600,53,C3179239,"['0.2002', '0.1359', '0.13', '-0.4255', '0.3472', '-0.3042', '0.1344', '1.256', '-0.6187', '-0.4727', '-0.4028', '0.1514', '0.1422', '-0.1772', '0.2803', '-0.2183', '0.2993', '-0.2279', '-0.461', '-0.6533', '-0.07556', '0.0166', '1.227', '-0.09045', '-0.2118', '0.1918', '-0.1959', '0.1495', '-0.699', '0.191', '0.4814', '-0.00546', '-0.628', '0.763', '0.0708', '0.04218', '0.3733', '-0.723', '-0.1603', '-0.4473', '0.1559', '0.1819', '0.566', '-0.522', '0.271', '-0.2654', '-0.4473', '0.0948', '0.004066', '-0.1118', '0.1993', '0.2827', '0.45', '-0.07086', '-0.2076', '-0.572', '0.0685', '-0.1808', '-0.3882', '-0.1891', '0.3975', '-0.09485', '-0.308', '-0.1049', '0.3154', '0.2181', '0.5854', '0.374', '-0.5586', '0.4084', '0.416', '-0.4153', '-0.2208', '-0.5474', '0.1293', '-0.502', '-0.3477', '0.4329', '0.5347', '-0.7144', '-0.2299', '-0.5957', '-0.11115', '0.8804', '-0.6626', '0.3652', '-0.08466', '-0.2778', '-0.2094', '-0.0651', '-0.388', '-0.284', '-0.416', '0.2426', '0.5063', '0.3684', '0.7573', '-0.2686', '0.2019', '-0.3684']",,,,,,,
mondo:0008157,Buschke-Ollendorff syndrome,"['osteopoikilosis, isolated', 'Buschke-Ollendorff syndrome', 'dermatofibrosis, disseminated, with osteopoikilosis', 'osteopoikilosis with melorheostosis', 'osteopathia condensans disseminata', 'Buschke Ollendorff syndrome', 'dermatofibrosis lenticularis disseminata with osteopoikilosis', 'Bos', 'dermatofibrosis, disseminated with osteopoikilosis', 'Dermatoosteopoikilosis', 'dermatofibrosis lenticularis disseminata, isolated', 'disseminated dermatofibrosis with osteopoikilosis', 'osteopoikilosis with or without melorheostosis']",0111536,166700,1306,,"['0.2673', '0.2666', '-0.2852', '-0.07635', '0.3765', '-0.3352', '-0.252', '0.328', '-0.4954', '-0.0939', '-0.1797', '0.465', '-0.03455', '0.41', '0.2964', '0.2834', '0.31', '-0.01415', '-0.09125', '-0.658', '-0.1025', '0.1316', '1.046', '-0.3564', '-0.11896', '0.2888', '-0.5415', '0.1509', '0.06647', '0.1833', '0.3635', '-0.875', '-0.03738', '0.362', '0.154', '-0.325', '0.0927', '-0.4624', '0.1818', '-0.2412', '0.692', '-0.6787', '-0.0924', '-0.5557', '0.4443', '-0.1884', '0.0243', '0.1697', '0.2712', '-0.405', '0.2139', '-0.247', '0.6313', '0.3494', '-0.5063', '-0.00881', '0.4668', '0.1453', '-0.3987', '-0.1886', '0.1262', '-0.0195', '-0.6387', '-0.1821', '0.10675', '0.1892', '0.199', '0.6416', '0.582', '0.4722', '0.010704', '-0.4905', '-0.011505', '-0.09546', '0.1973', '0.454', '-0.3074', '0.4285', '-0.2374', '-0.7656', '-0.159', '-0.1095', '0.11676', '0.0918', '-0.2664', '-0.0228', '0.2144', '0.02122', '-0.1321', '-0.01037', '-0.0912', '0.12476', '-0.2366', '-0.01352', '0.2727', '0.1359', '0.4011', '-0.374', '0.1847', '0.0513']",,,C537415,,,,
mondo:0008158,dacryocystitis-osteopoikilosis syndrome,"['Gunal Seber Basaran syndrome', 'osteopoikilosis and dacryocystitis', 'dacryocystitis osteopoikilosis', 'Gunal-Seber-Basaran syndrome']",,166705,1562,C1833698,,,,C536061,,,,
mondo:0008159,postmenopausal osteoporosis,"['bone mineral density quantitative trait locus', 'osteoporosis, postmenopausal']",,,,C0029458,"['0.3804', '-0.2274', '0.1438', '0.643', '0.3257', '-0.597', '-0.538', '0.8223', '-0.713', '-0.4604', '0.2144', '0.5938', '0.11993', '0.574', '-0.392', '-0.2727', '-0.0956', '0.4768', '-0.94', '-0.1562', '-0.1411', '-0.5493', '0.1812', '-0.4636', '0.24', '-0.3733', '0.132', '-0.755', '-0.508', '-0.03125', '0.539', '-0.578', '-0.2974', '-0.292', '-0.06665', '-0.1683', '-0.0326', '-0.7827', '0.2693', '-0.5215', '0.03638', '0.003956', '0.2527', '-0.2646', '0.7295', '-0.545', '0.1462', '0.1782', '0.317', '0.886', '0.6504', '0.0925', '0.3445', '-0.010796', '-0.317', '-0.7734', '-0.2654', '0.3682', '-0.386', '-0.06064', '0.308', '0.0691', '-0.965', '-0.4949', '-0.1178', '0.8545', '0.5483', '0.76', '-0.2542', '-0.366', '0.727', '-0.1681', '-0.07495', '-0.443', '0.6216', '0.6694', '-0.2288', '0.6216', '-0.10803', '0.08813', '-0.122', '-0.2935', '0.2487', '0.4568', '-0.591', '0.6562', '0.2578', '-0.07947', '1.215', '0.1399', '-0.4827', '-0.309', '-1.005', '-0.1443', '0.5073', '-0.356', '0.01147', '-0.548', '-0.2805', '-0.454']",,0003854,D015663,,,,
mondo:0008160,osteosclerosis with ichthyosis and fractures,"['cortical thickening of long bones with bowing and ichthyosis', 'osteosclerosis with ichthyosis and fractures']",,166740,,C1833697,,,,C563483,,,,
mondo:0008161,otodental syndrome,"['otodental syndrome with coloboma', 'otodental dysplasia', 'globodontia', 'oculootodental syndrome', 'chromosome 11q13 deletion syndrome', 'otodental dysplasia chromosome deletion syndrome', 'otodental syndrome']",,166750,2791,C1833693,,,,,,,,
mondo:0008162,"otitis media, susceptibility to","['otitis media, susceptibility to', 'OMS', 'come/Rom', 'otitis Media, chronic/recurrent']",,166760,,,"['-0.006588', '0.05344', '0.01258', '-0.07306', '0.01907', '-0.0873', '0.11255', '0.0828', '-0.04544', '-0.0455', '-0.02078', '0.001191', '-0.05338', '0.02841', '-0.04114', '-0.0593', '-0.003267', '-0.04343', '-0.03848', '-0.1361', '0.01093', '-0.03253', '0.089', '-0.03314', '0.000539', '-0.010735', '-0.05698', '0.02696', '-0.04187', '-0.0743', '0.0766', '0.00804', '0.10443', '0.0363', '0.02594', '-0.0565', '-0.0683', '-0.0705', '-0.0535', '-0.0959', '-0.0306', '-0.02516', '0.0852', '-0.04797', '-0.003353', '-0.06024', '-0.01968', '0.05444', '-0.02916', '0.08075', '-0.08844', '-0.012726', '0.0709', '-0.02998', '-0.006493', '-0.002764', '0.0632', '-0.1035', '-0.0742', '0.02151', '0.06683', '0.0897', '-0.0599', '0.06506', '0.04828', '-0.002209', '0.07135', '0.1123', '-0.05728', '0.1271', '-0.0873', '0.01785', '0.0141', '-0.1087', '0.03802', '0.01941', '0.0341', '-0.0341', '-0.004627', '-0.02852', '-0.04672', '-0.03232', '-0.02702', '0.1205', '-0.0403', '0.05115', '0.065', '0.05563', '0.12195', '-0.03108', '0.03784', '0.0911', '-0.04547', '0.05304', '0.1671', '0.09534', '0.0851', '-0.0894', '-0.01933', '0.02437']",,,,,,,
mondo:0008163,otofaciocervical syndrome,"['OFC syndrome', 'Fara-Chlupackova syndrome']",,,2792,C2931416,"['-0.3752', '-0.03943', '0.594', '-0.905', '-0.1517', '-0.234', '0.4717', '0.6274', '-0.82', '-0.2437', '-0.3022', '-0.095', '0.395', '-0.0325', '-0.4268', '-0.2272', '0.1733', '-0.3848', '-0.2961', '-0.483', '0.4', '0.4973', '0.431', '0.02122', '0.1543', '0.0447', '0.1255', '-0.3777', '0.465', '-0.721', '0.366', '-0.4163', '0.2905', '0.2278', '0.465', '0.1471', '0.2175', '-0.329', '0.0153', '-0.6494', '0.2406', '0.1069', '0.2869', '-0.2737', '-0.2388', '-0.6343', '0.0817', '0.1609', '0.06015', '0.549', '-0.4463', '-0.0631', '0.2284', '0.1012', '-0.609', '-0.1888', '-0.2032', '0.009575', '0.354', '0.3445', '-0.05518', '0.0313', '-0.7114', '0.0913', '-0.3376', '0.0985', '0.3098', '0.9824', '-0.353', '0.5527', '0.0936', '0.339', '0.1461', '-0.1876', '-0.3293', '0.1655', '0.1282', '-0.3423', '-0.4531', '-0.2783', '0.135', '0.14', '0.3376', '0.6704', '-0.1385', '-0.0168', '-0.5854', '0.7524', '0.4038', '0.6904', '0.1343', '0.497', '0.4912', '0.2625', '0.5615', '-0.559', '0.6094', '-0.7974', '0.3318', '0.1696']",,,C563481,,,,
mondo:0008164,otosclerosis 1,"['otosclerosis 1', 'OTSC1', 'OTS']",,166800,,CN032031,,,,,,,,
mondo:0008165,southeast Asian ovalocytosis,"['stomatocytic elliptocytosis', 'Melanesian ovalocytosis', 'elliptocytosis, stomatocytic hereditary', 'Melanesian elliptocytosis', 'ovalocytosis, SA type', 'ovalocytosis, Malaysian-Melanesian-Filipino type', 'ovalocytosis, hereditary hemolytic', 'ovalocytosis, southeast Asian', 'he, stomatocytic', 'hereditary ovalocytosis', 'elliptocytosis 4', 'sao']",,166900,98868,C1862323,"['-0.05804', '0.04614', '-0.1691', '-0.2566', '-0.11273', '-0.522', '-0.6875', '0.8257', '0.6074', '-0.328', '0.03078', '0.11206', '-0.2563', '0.372', '-0.2349', '0.000773', '-0.3164', '-0.1974', '0.2588', '-0.609', '-0.6025', '-0.2893', '0.6416', '0.4873', '0.3267', '0.01889', '0.01543', '-0.0859', '0.52', '-0.2747', '0.2314', '-0.3428', '-0.01186', '0.367', '-0.3677', '0.2106', '-0.4329', '-0.705', '-0.02142', '-0.3574', '-0.1371', '-0.3179', '0.2041', '-0.2499', '-0.44', '-0.2126', '-0.59', '0.06174', '0.6064', '-0.3267', '0.5703', '-0.4424', '0.0585', '-0.386', '-0.02231', '0.1003', '0.446', '-0.2893', '-0.4182', '-0.01778', '-0.04718', '-0.1627', '-0.0882', '-0.2201', '-0.08575', '-0.3535', '0.8647', '0.3828', '0.0824', '0.5947', '0.2693', '-0.4116', '-0.447', '0.1874', '0.0617', '0.4177', '0.1855', '-0.2238', '0.05615', '-0.3904', '-0.4307', '-0.2651', '0.0009575', '-0.1261', '0.01133', '-0.1057', '0.1641', '0.386', '0.4924', '-0.4924', '0.6147', '0.07526', '0.4949', '-0.2656', '0.761', '0.4368', '-0.2676', '-0.6074', '-0.106', '-0.2163']",,,,282.1,,,
mondo:0008166,"ovalocytosis, hereditary hemolytic, with defective erythropoiesis","['ovalocytosis, hereditary hemolytic, with defective erythropoiesis']",,166910,,C1833689,,,,C563479,,,,
mondo:0008167,dermoid cyst of ovary,"['dermoid cyst (& [ovarian])', 'ovarian dermoid cyst', 'teratoma, ovarian', 'dermoid cyst, ovarian', 'dermoid cyst of ovary', 'ovary dermoid cyst', 'dermoid cyst of the ovary']",5117,166950,,C0237020,,C3856,,C562731,,,,
mondo:0008168,ovarian fibroma,"['fibroma of ovary', 'ovarian fibroma (disease)', 'fibroma of the ovary', 'ovarian fibroma', 'ovarian fibromata']",,166970,314473,C0149951,,C3498,,C562391,,,10064257,0010618
mondo:0008169,"osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension","['osteochondrodysplasia, rhizomelic, with callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension', 'osteochondrodysplasia with rhizomelia, platyspondyly, callosal agenesis, thrombocytopenia, hydrocephalus, and hypertension']",,166990,,C1833688,,,,C563478,,,,
mondo:0008170,ovarian cancer,"['cancer of the ovary', 'tumour of the ovary', 'ovarian cancer, epithelial', 'ovarian cancer', 'malignant tumour of ovary', 'malignant neoplasm of ovary', 'malignant ovary neoplasm', 'malignant ovarian tumor', 'primary ovarian cancer', 'ovary neoplasm', 'ovarian malignant tumour', 'malignant neoplasm of the ovary', 'malignant tumour of the ovary', 'ovarian malignant tumor', 'malignant ovarian neoplasm', 'cancer of ovary', 'tumor of the ovary', 'ovarian cancer, somatic', 'malignant ovarian tumour', 'ovarian neoplasm', 'malignant tumor of ovary', 'malignant tumor of the ovary', 'ovary cancer']",2394,167000,213500,,"['0.003597', '0.0305', '-0.002914', '-0.008835', '0.00971', '-0.06223', '0.0234', '0.03928', '-0.03806', '-0.04953', '0.01183', '0.013016', '-0.00875', '0.01186', '-0.0272', '-0.062', '0.003326', '-0.02525', '-0.02219', '-0.0809', '-0.01152', '-0.02408', '0.03656', '-0.04822', '0.03857', '-0.02155', '-0.003975', '0.01149', '-0.003298', '-0.06635', '0.06586', '0.01642', '0.06006', '-0.0179', '0.005875', '-0.02104', '-0.02817', '-0.00033', '0.00649', '-0.02379', '0.01343', '-0.02924', '0.01105', '-0.02225', '0.009186', '-0.03323', '-0.0102', '0.0386', '0.01997', '0.03214', '-0.001783', '0.01145', '0.00826', '0.04813', '-0.0501', '-0.01249', '0.03078', '-0.02643', '-0.0628', '-0.002453', '0.05338', '0.007454', '-0.004395', '0.02296', '-0.00978', '0.02095', '0.04337', '0.03766', '-0.03708', '0.02693', '-0.00965', '0.02621', '0.02194', '-0.02531', '0.0369', '0.0006356', '0.01354', '-0.02199', '-0.00953', '-0.04987', '-0.02293', '-0.015335', '-0.02528', '0.02518', '-0.03506', '-0.02823', '0.0305', '0.00933', '0.0449', '0.006817', '0.001229', '0.06354', '-0.00933', '0.002398', '0.08936', '0.02623', '0.04218', '-0.0402', '-0.01674', '0.01743']",C7431,,D010051,183.0,,,
mondo:0008171,nephrolithiasis,"['kidney stone', 'Stone - kidney/ureter', 'calculus of kidney and ureter', 'nephrolithiasis, calcium oxalate', 'kidney stones', 'renal calculi', 'urolithiasis, calcium oxalate', 'CAON']",585,,,C0392525,"['-0.153', '0.05893', '0.0696', '0.1715', '0.1221', '-0.05075', '-0.2566', '0.3281', '-0.1932', '0.01938', '-0.1841', '-0.02441', '-0.1106', '0.3452', '-0.2284', '-0.273', '0.04456', '-0.11566', '0.0632', '-0.367', '-0.01994', '-0.2391', '0.172', '0.00839', '0.2438', '-0.3267', '-0.131', '0.009186', '0.12134', '0.03296', '0.1836', '-0.334', '0.10236', '-0.1375', '0.0448', '-0.1497', '-0.115', '0.05106', '0.2339', '-0.0924', '0.0823', '-0.2615', '0.1863', '-0.2388', '-0.1498', '-0.0843', '-0.02911', '-0.02489', '0.2874', '0.1986', '-0.03308', '-0.07404', '0.199', '-0.004887', '-0.2756', '-0.1748', '0.2334', '0.128', '-0.3738', '0.01421', '0.4414', '0.001', '-0.343', '-0.1357', '0.08954', '-0.213', '0.3413', '0.2742', '-0.10614', '-0.033', '0.2216', '-0.0405', '0.1298', '-0.09973', '0.04596', '0.1895', '-0.005817', '0.363', '-0.0951', '-0.2285', '-0.3577', '-0.0946', '-0.04944', '0.02809', '-0.2394', '-0.1758', '-0.05164', '-0.3203', '0.358', '0.07733', '-0.1276', '0.2292', '-0.181', '0.002226', '0.4976', '0.11993', '0.10596', '-0.2421', '-0.3506', '0.0639']",C114667,0004253,D053040,592,,,
mondo:0008172,"hypertrophic osteoarthropathy, primary, autosomal dominant","['pachydermoperiostosis, autosomal dominant', 'PDP, autosomal dominant', 'PHOAD', 'hypertrophic osteoarthropathy, primary, autosomal dominant', 'Pho, autosomal dominant']",,167100,,C2674695,,,,,,,,
mondo:0008173,pachyonychia congenita 1,"['pachyonychia congenita, Jadassohn-Lewandowsky type', 'pachyonychia congenita, Jadassohn-Lewandowsky type, formerly', 'Jadassohn-Lewandowsky syndrome', 'pachyonychia congenita caused by mutation in KRT16', 'Jadassohn-Lewandowsky syndrome, formerly', 'pachyonychia congenita type 1', 'PC1', 'KRT16 pachyonychia congenita', 'pachyonychia congenita 1']",,167200,,,,,,,,,,
mondo:0008174,pachyonychia congenita 2,"['pachyonychia congenita type 2', 'pachyonychia congenita, Jackson-Lawler type', 'pachyonychia congenita, Jackson-Lawler type, formerly', 'pachyonychia congenita caused by mutation in KRT17', 'pachyonychia congenita 2', 'PC2', 'KRT17 pachyonychia congenita']",,167210,,,,,,,,,,
mondo:0008175,pacman dysplasia,"['pacman dysplasia', 'Pacman syndrome', 'epiphyseal stippling syndrome-osteoclastic hyperplasia syndrome', 'epiphyseal stippling with osteoclastic hyperplasia']",,167220,1952,C1833676,,,,C538095,,,,
mondo:0008176,Paget disease of bone 3,"['Paget disease of bone 3', 'familial Paget disease of bone', 'Paget disease of bone type 3', 'PDB3', 'Paget disease of bone, familial']",0081366,167250,,C4085252,,,,,,,,
mondo:0008177,extramammary Paget disease,"['EMPD', 'extramammary Paget disease', 'Paget disease Extramammary', 'cutaneous Paget^s disease', 'Paget^s disease of the skin', 'Extramammary Paget^s disease', 'Paget^s skin disease', 'Paget^s disease of skin', 'Paget disease, EXTRAMAMMARY']",,167300,2800,C0030186,,C3302,1000249,D010145,,,10068223,
mondo:0008178,inclusion body myopathy with Paget disease of bone and frontotemporal dementia type 1,"['inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia 1', 'lower motor neuron degeneration with Paget-like bone disease', 'pagetoid amyotrophic lateral sclerosis', 'inclusion body myopathy with early-onset Paget disease with or without frontotemporal dementia type 1', 'muscular dystrophy, limb-girdle, with Paget disease of bone', 'inclusion body myopathy with early-onset paget disease and frontotemporal dementia 1', 'IBMPFD1', 'multisystem proteinopathy 1']",0111385,167320,,,,C122663,,C563476,,,,
mondo:0008179,paroxysmal extreme pain disorder,"['Pexpd', 'PEPD', 'submandibular, ocular, and rectal pain with flushing', 'familial rectal syndrome', 'familial rectal pain', 'rectal pain, familial', 'pain, submandibular, ocular, and rectal, with flushing', 'paroxysmal extreme pain disorder']",0111537,167400,46348,C1833661,"['-0.5947', '-0.0009003', '-0.577', '-0.1794', '-0.7593', '0.07947', '0.4312', '0.5596', '-0.4897', '0.3108', '-0.2091', '0.3303', '0.09174', '0.1952', '-0.0704', '0.35', '0.303', '-0.1774', '-0.0665', '-0.8486', '0.07214', '-0.2303', '-0.2318', '-0.458', '-0.2395', '0.09015', '0.2', '-0.111', '0.0804', '0.1317', '0.5576', '-0.2537', '-0.00298', '0.1805', '-0.3162', '0.4426', '-0.2878', '0.1732', '-0.07855', '0.2678', '0.231', '-0.421', '-0.1499', '0.2234', '0.606', '0.1146', '-0.4146', '0.1476', '0.39', '1.043', '-0.4595', '0.1793', '0.1241', '-0.217', '-0.0515', '0.339', '0.775', '0.1792', '-0.3289', '-0.2357', '-0.08276', '0.0868', '0.3997', '-0.2462', '0.02306', '0.171', '0.701', '0.4902', '0.1636', '0.06055', '-0.439', '0.1252', '-0.2302', '0.0989', '0.4434', '0.746', '0.548', '0.5386', '-0.1395', '0.147', '0.1288', '0.03177', '0.3665', '0.369', '0.4114', '-0.161', '0.0978', '0.1631', '-0.1974', '0.8633', '-0.3127', '-0.2115', '-0.2152', '0.4836', '0.83', '0.04022', '0.0363', '-0.4263', '-0.3367', '-0.02065']",C125385,,C563475,349.89,,,
mondo:0008180,congenital velopharyngeal incompetence,"['velopharyngeal incompetence', 'palatopharyngeal incompetence', 'velopharyngeal insufficiency']",,167500,2291,C0042454,,,,D014681,,,,
mondo:0008181,"palmaris longus muscle, absence of","['palmaris longus muscle, absence of']",,167600,,,,,,,,,,
mondo:0008182,nasopalpebral lipoma-coloboma syndrome,"['NPLCS', 'palpebral coloboma-lipoma syndrome', 'NASOPALPEBRAL lipoma-coloboma syndrome', 'nasopalpebral lipoma-coloboma syndrome', 'Nasopalpebral lipoma coloboma syndrome', 'palpebral coloboma lipoma syndrome']",,167730,2399,C1868660,,,,C538338,,,,
mondo:0008183,annular pancreas,"['pancreas, annular']",0060850,167750,675,C0149955,,C98813,,C536376,,Q45.1,10071757,
mondo:0008184,"pancreas, dorsal, agenesis of","['pancreas, dorsal, agenesis of', 'congenital short pancreas', 'partial agenesis of the dorsal pancreas', 'pancreas agenesis, dorsal', 'complete agenesis of the dorsal pancreas', 'agenesis of the dorsal pancreas']",,167755,,C1868659,,,,C538109,,,,
mondo:0008185,hereditary chronic pancreatitis,"['pancreatitis, calcific', 'Hp', 'pancreatitis, chronic pancreatitis, chronic, susceptibility to, included', 'HPC', 'pancreatitis, chronic, protection against', 'pancreatitis, chronic, protection against, included', 'pancreatitis, chronic, susceptibility to', 'familial pancreatitis', 'PCTT', 'pancreatitis, chronic', 'hereditary chronic pancreatitis', 'pancreatitis, hereditary', 'hereditary pancreatitis', 'autosomal dominant hereditary pancreatitis', 'pancreatitis, calcific, included']",,167800,676,,"['0.263', '0.1603', '-0.3987', '0.3032', '-0.623', '-0.068', '0.535', '0.4238', '-0.5684', '0.1041', '0.3394', '-0.443', '0.2703', '0.4443', '-0.6846', '-0.1335', '-0.139', '0.676', '-0.383', '-0.1261', '-0.1404', '-0.193', '0.6577', '-0.4785', '0.2318', '0.3315', '0.3474', '0.4114', '0.579', '-0.8726', '-0.1373', '-0.01196', '0.4956', '-0.1295', '0.02286', '0.0311', '-0.6533', '-0.02318', '0.3076', '0.1687', '-0.4946', '-0.1621', '0.1907', '0.1631', '-0.513', '-0.4106', '0.1731', '-0.6387', '0.04337', '0.07196', '-0.1355', '-0.1552', '0.295', '-0.3557', '0.4817', '0.4663', '-0.1373', '-0.04895', '-0.55', '-0.4636', '0.5596', '0.407', '0.3252', '-0.654', '-0.0905', '0.1985', '0.5415', '0.5137', '-0.1373', '0.00716', '-0.0896', '0.164', '0.3206', '-0.3496', '0.8027', '0.3364', '0.179', '0.7676', '-0.2227', '-0.279', '-0.829', '-0.2969', '-0.2133', '-0.1855', '0.264', '0.4832', '0.6724', '0.534', '0.626', '-0.4998', '0.1787', '-0.3044', '-0.3794', '0.2822', '0.88', '0.04865', '0.02371', '-0.813', '-0.5205', '0.7144']",C95436,,C537262,577.8,,,
mondo:0008186,pancytopenia and occlusive vascular disease,['pancytopenia and occlusive vascular disease'],,167850,,C1868652,,,,C566836,,,,
mondo:0008187,panic disorder 1,"['panic disorder syndrome 1', 'panic disorder', 'panic disorder susceptibility locus, chromosome 13Q-related', 'PAND1', 'panic disorder with bladder conditions', 'panic disorder with Joint laxity', 'panic disorder, susceptibility to', 'panic disorder 1']",,167870,,,,,,,,,,
mondo:0008188,"papillomatosis, confluent and reticulated","['papillomatosis, reticulated and confluent, of Gougerot and Carteaud', 'papillomatosis, confluent and reticulated', 'papillomatosis, familial cutaneous', 'carp']",,167900,,C0263385,,,,C566832,,,,
mondo:0008189,"papillomatosis, florid, of nipple","['papillomatosis, florid, of nipple', 'florid papillomatosis of the nipple', 'erosive adenomatosis of nipple', 'papillomatosis florid of nipple', 'erosive nipple adenomatosis', 'florid papillomatosis', 'erosive adenomatosis of the nipple']",,167950,,C1868647,,C4383,,C537167,,,,
mondo:0008192,paragangliomas 1,"['carotid body tumours', 'chemodectomas', 'paragangliomas 1', 'paragangliomas, familial, 1', 'carotid body tumors', 'glomus jugulare tumours', 'paragangliomas 1, with or without deafness', 'SDHD paraganglioma', 'paraganglioma caused by mutation in SDHD', 'paraganglioma, carotid body', 'PGL1', 'glomus tumors, familial, 1', 'paragangliomas type 1', 'Paragangliomata', 'paragangliomas, familial nonchromaffin, 1', 'glomus jugulare tumors', 'paragangliomas with sensorineural hearing loss']",,168000,,C0017671,,,,,,,,
mondo:0008193,"paralysis agitans, juvenile, of Hunt","['Parkinson disease, juvenile, of Hunt', 'paralysis agitans, juvenile, of Hunt']",,168100,,,,,,C562469,333.0,,,
mondo:0008194,Paramolar tubercle of bolk,"['Paramolar tubercle of bolk', 'bolk cusp']",,168200,,,,,,,,,,
mondo:0008195,paramyotonia congenita of Von Eulenburg,"['paralysis periodica Paramyotonica', 'paramyotonia congenita of Von Eulenburg', 'Eulenburg disease', 'PMC', 'Von Eulenburg paramyotonia congenita', 'paramyotonia congenita without cold paralysis', 'paramyotonia congenita', 'paramyotonia congenita of VON Eulenburg', 'myotonia congenita intermittens']",0111538,168300,684,,"['-0.3845', '0.2349', '0.1643', '-0.732', '-0.217', '-0.07275', '0.1268', '-0.01976', '-0.3354', '-0.2279', '-0.3237', '0.2693', '-0.1609', '-0.1119', '0.286', '0.1238', '-0.1862', '-0.2568', '-0.2059', '-0.8755', '0.1427', '-0.3684', '0.3662', '0.1986', '0.1259', '0.2191', '0.272', '-0.5815', '-0.0465', '-0.09937', '0.11804', '0.0956', '0.12134', '-0.2313', '-0.2986', '-0.1562', '0.1641', '0.12366', '0.2515', '-0.3135', '-0.3765', '-0.302', '0.2058', '0.1692', '0.563', '-0.2388', '-0.1168', '0.4592', '0.3916', '0.2355', '-0.0549', '-0.1292', '0.03735', '-0.1633', '-0.1677', '-0.4048', '0.6567', '0.1786', '-0.3667', '0.04877', '0.0833', '-0.01041', '0.0866', '-0.1371', '-0.04456', '-0.2725', '0.1646', '0.03308', '-0.6045', '-0.02843', '-0.93', '-0.4478', '0.1284', '0.0735', '0.5576', '0.4778', '0.05316', '0.2834', '-0.04752', '-0.3945', '0.413', '0.1221', '0.255', '-0.0867', '-0.02826', '0.1342', '0.11115', '0.5894', '0.366', '0.1605', '-0.2922', '0.03955', '0.4495', '-0.02136', '0.4893', '0.06616', '0.2961', '-0.5073', '-0.256', '0.05173']",C122790,,,359.29,,,
mondo:0008196,parastremmatic dwarfism,"['parastremmatic dwarfism', 'Parastremmatic dysplasia']",0111539,168400,2646,,"['-0.4907', '0.1726', '-0.01572', '-0.576', '0.4993', '-0.2786', '0.1385', '1.236', '-0.9453', '-0.703', '0.3828', '-0.2869', '0.4185', '0.554', '-0.02434', '-0.5684', '0.5127', '0.1842', '-0.723', '-1.138', '-1.346', '0.1226', '1.125', '-0.10925', '-0.00011486', '-0.3313', '-0.3572', '-0.2678', '0.558', '-0.1677', '0.06696', '-0.498', '-0.1138', '0.1298', '-0.4006', '-0.4343', '0.05966', '-0.1096', '0.4143', '-0.3047', '7.76e-05', '0.2676', '-0.6187', '-0.511', '0.2878', '-0.1318', '-0.10504', '0.263', '0.915', '-0.1332', '0.03854', '-0.227', '-0.7393', '0.549', '-0.06027', '-0.7217', '-0.4863', '-0.2532', '1.05', '0.2544', '-0.04257', '0.4038', '-0.405', '0.2247', '-0.01265', '1.243', '-0.1345', '0.285', '-0.478', '0.4346', '-0.4514', '-0.1235', '0.4346', '-1.17', '-0.1715', '0.7383', '-0.2988', '0.842', '-0.2795', '0.341', '-0.516', '-0.11816', '-0.2983', '0.0557', '0.4182', '-0.2129', '-0.06384', '-0.0586', '0.6567', '0.7666', '-0.2145', '-0.1881', '-0.4958', '-0.5645', '0.524', '-0.1652', '0.1405', '-0.0936', '0.702', '0.186']",,,C537172,,,,
mondo:0008197,parietal foramina 1,"['parietal foramina, symmetric', 'PFM', 'PFM1', 'cranium bifidum, hereditary', 'catlin Marks', 'MSX2 parietal foramina', 'parietal foramina caused by mutation in MSX2', 'cranium bifidum occultum', 'foramina parietalia permagna', 'parietal foramina', 'parietal foramina 1']",,168500,,,,,,C566827,,,,
mondo:0008198,parietal foramina with cleidocranial dysplasia,"['parietal foramina with clavicular hypoplasia', 'parietal foramina with cleidocranial dysplasia', 'parietal foramina with cleidocranial dysostosis', 'cleidocranial dysplasia with parietal foramina', 'PFMCCD']",,168550,251290,C1868597,"['-0.5464', '-0.1483', '0.4033', '-0.683', '0.11035', '-0.1818', '-0.4465', '1.022', '-0.657', '0.3096', '-0.2827', '-0.166', '0.12085', '-0.03873', '-0.07556', '0.0274', '0.8086', '-0.404', '-0.773', '-0.614', '0.3423', '-0.165', '0.4624', '-0.211', '0.76', '-0.0855', '-0.1411', '0.1159', '0.3865', '-0.4473', '0.12103', '0.014786', '0.1453', '0.1548', '0.4219', '-0.233', '-0.3726', '-0.5205', '0.2822', '-0.5127', '0.432', '0.04495', '0.02606', '-0.4866', '0.1361', '-0.612', '0.2109', '0.2947', '0.05606', '-0.0196', '0.256', '0.009514', '-0.03833', '0.591', '-0.4915', '-0.787', '-0.326', '-0.0461', '-0.124', '0.2455', '0.4548', '-0.1267', '0.0905', '-0.1852', '-0.1805', '0.4316', '0.362', '0.0775', '-0.475', '0.396', '-0.1388', '0.1043', '0.2047', '0.09186', '-0.1813', '0.05157', '0.428', '0.1011', '-0.581', '-0.1483', '0.164', '0.05014', '0.3394', '0.7695', '-0.3513', '0.03326', '-0.1047', '0.581', '0.326', '0.3604', '-0.1982', '0.25', '0.1123', '0.1334', '0.7173', '-0.1836', '0.8555', '-0.5015', '0.713', '0.02936']",,,C566825,,,,
mondo:0008199,late-onset Parkinson disease,"['PD', 'late-onset Parkinson disease', 'late onset Parkinson disease', 'Parkinson disease, late-onset, susceptibility to, Multifactorial', 'Parkinson disease, age of onset, modifier, Multifactorial', 'LOPD', 'Parkinson disease, late-onset', 'autosomal dominant late-onset Parkinson disease', 'PARK', 'late onset Parkinson^s disease', 'Parkinson disease, susceptibility to, Multifactorial', 'hereditary late-onset Parkinson disease']",0060892,168600,411602,C3160718,"['-0.01364', '0.0767', '-0.02486', '-0.009796', '0.0048', '-0.11523', '0.002659', '0.06076', '-0.09393', '-7.8e-06', '-0.003246', '0.001489', '-0.0291', '0.04718', '0.02939', '-0.06555', '-0.02695', '-0.06726', '-0.0434', '-0.1467', '-0.008095', '-0.0769', '0.0263', '-0.03964', '0.01738', '-0.04633', '-0.01837', '-0.03467', '-0.003098', '-0.0385', '0.0578', '0.0161', '0.05978', '0.01444', '0.0405', '-0.03934', '-0.02846', '-0.03738', '-0.000862', '-0.03053', '0.0417', '-0.0445', '0.072', '0.02618', '0.0454', '-0.06537', '-0.0174', '0.03696', '0.03543', '0.03784', '-0.005554', '0.01726', '0.006397', '-0.00852', '-0.004635', '-0.085', '0.07684', '-0.05362', '-0.1092', '0.002382', '0.06604', '0.02884', '0.02432', '0.006134', '0.005707', '0.0323', '0.11566', '0.0697', '-0.03708', '0.0826', '-0.04282', '-0.02324', '0.05048', '-0.04074', '0.02452', '0.05017', '0.0006123', '0.00982', '-0.0758', '-0.02455', '-0.001785', '-0.0402', '-0.02861', '0.05728', '-0.012024', '-0.01018', '0.0372', '0.01519', '0.0907', '0.01278', '0.0435', '0.03546', '0.03546', '0.03943', '0.1687', '0.0572', '0.05472', '-0.03494', '-0.02507', '0.005733']",,,,,,,
mondo:0008200,autosomal dominant Parkinson disease 1,"['atypical Parkinson disease', 'autosomal dominant Parkinson^s disease 1', 'Parkinson disease 1, autosomal dominant Lewy body', 'autosomal dominant Parkinson disease type 1', 'Parkinson disease 1, autosomal dominant', 'PARK1']",0060367,168601,171695,,,,,C566823,,,,
mondo:0008201,Perry syndrome,"['Parkinsonism with alveolar hypoventilation and mental depression', 'Perry syndrome', 'parkinsonism with alveolar hypoventilation and mental depression']",0060486,168605,178509,C1868594,"['0.0465', '0.4426', '-0.2715', '0.6113', '-0.429', '-0.594', '0.4895', '1.2295', '0.02136', '-0.1857', '0.4895', '-0.1113', '-0.0835', '-0.05087', '0.5483', '-0.3406', '-0.0402', '0.05426', '-0.4165', '-0.783', '-0.0834', '-0.4553', '-0.0288', '-0.5244', '-0.2966', '-0.0712', '-0.4834', '-0.3953', '-0.0943', '-0.5215', '0.7603', '0.288', '-0.10443', '-0.1376', '-0.343', '-0.374', '-0.4404', '-0.364', '-0.0865', '0.0989', '0.1785', '-0.3367', '0.374', '-0.3892', '0.2374', '0.3655', '-0.8086', '-0.3413', '-0.1995', '0.573', '-0.3762', '0.703', '-0.3665', '-0.63', '0.8525', '0.2491', '0.5156', '-0.02866', '-0.2345', '-0.137', '0.5103', '0.5903', '0.2047', '-0.05865', '-0.3845', '0.4568', '0.04117', '0.1666', '0.109', '0.46', '-0.4253', '-0.1018', '-0.04828', '-0.1881', '0.2014', '0.1929', '0.124', '-0.3215', '-0.1625', '-0.3833', '-0.2383', '-0.2505', '-0.04987', '1.035', '0.08435', '0.6675', '0.0805', '0.1371', '0.4038', '-0.003016', '0.5405', '0.0625', '-0.123', '0.4905', '0.02216', '-0.2452', '0.141', '-0.4812', '0.1342', '0.1118']",,,C566822,348.89,,,
mondo:0008202,"Parotidomegaly, hereditary bilateral","['Parotidomegaly, hereditary bilateral']",,168800,,C1868590,,,,C566821,,,,
mondo:0008203,Passovoy factor defect,['Passovoy factor defect'],,168830,,C3149707,,,,,,,,
mondo:0008205,patella aplasia/hypoplasia,"['patella aplasia or hypoplasia', 'patella aplasia-hypoplasia', 'absent patella', 'familial absence of the patella', 'familial aplasia of the patella (subtype)', 'PTLAH']",,168860,86789,,,,,C535568,,,,
mondo:0008206,benign paroxysmal tonic upgaze of childhood with ataxia,"['Ouvrier-Billson syndrome', 'Ouvrier Billson syndrome', 'paroxysmal tonic upgaze, benign childhood, with ataxia']",,168885,1179,C1868576,,,,C566817,,,,
mondo:0008207,chondromalacia patellae,"['patella chondromalacia', 'softening of articular cartilage of patella', 'chondromalacia patellae', 'familial chondromalacia patellae', 'chondromalacia of patella', 'patella, chondromalacia OF']",13357,168900,1428,C0008475,,,,D046789,717.7,M22.4,,
mondo:0008208,"patella, familial recurrent dislocation of","['patella, familial recurrent dislocation of']",,169000,,C1868575,,,,C566816,,,,
mondo:0008209,Char syndrome,"['patent ductus arteriosus with facial dysmorphism and abnormal fifth digits', 'patent ductus arteriosus with Facial Dysmorphism and abnormal fifth digits', 'Char', 'CHAR syndrome', 'CHAR', 'Char syndrome']",0060563,169100,46627,C1868570,"['0.1769', '-0.5464', '0.0842', '0.2065', '-0.2318', '-0.2351', '0.4277', '0.7266', '-0.554', '-0.5737', '-0.3098', '-0.4133', '-0.1201', '0.5576', '-0.3406', '-0.1566', '0.0882', '-0.2524', '-0.2437', '-0.83', '-0.4016', '0.6514', '0.4067', '-0.10156', '0.2795', '-0.1067', '-0.2019', '0.9204', '0.754', '-0.1896', '0.461', '-0.05685', '0.04318', '0.1664', '0.3071', '-0.6064', '-0.0437', '-0.5063', '-0.03137', '-0.7275', '0.07605', '0.0453', '0.1112', '0.07355', '0.513', '-0.4475', '-0.1774', '0.672', '-0.4385', '-0.2156', '-0.566', '0.0958', '-0.0692', '0.2423', '-0.563', '-0.499', '-0.1505', '0.2416', '0.0507', '0.01974', '-0.00904', '0.010345', '-0.3108', '0.1447', '0.2435', '-0.0764', '0.2062', '0.33', '-0.3938', '0.2776', '-0.581', '0.1709', '-0.010956', '0.279', '-0.001675', '0.07', '0.3767', '-0.6514', '-0.6543', '-0.05725', '0.11035', '0.236', '-0.2355', '0.666', '0.1166', '0.1913', '-0.4783', '0.707', '-0.0762', '-0.0935', '0.295', '0.3276', '0.0937', '0.2578', '0.495', '-0.4458', '0.4546', '-0.763', '0.3254', '0.3242']",,,C566815,759.89,,,
mondo:0008210,patterned macular dystrophy 1,"['butterfly-shaped pigmentary maculary dystrophy 1', 'patterned macular dystrophy caused by mutation in PRPH2', 'patterned macular dystrophy type 1', 'macular dystrophy, patterned, 1', 'patterned dystrophy of retinal pigment epithelium', 'macular dystrophy, butterfly-shaped pigmentary', 'macular dystrophy, patterned, type 1', 'macular dystrophy, butterfly-Shaped pigmentary', 'butterfly dystrophy of retinal pigment epithelium', 'PRPH2 patterned macular dystrophy', 'butterfly-shaped pigment dystrophy of the fovea', 'MDPT1']",0060866,169150,,,,,,,,,,
mondo:0008211,"pseudoleprechaunism syndrome, Patterson type","['Patterson syndrome', 'Patterson^s leprechaunoid syndrome', 'Patterson pseudoleprechaunism syndrome']",,169170,2976,C1868546,,,,C536310,,,,
mondo:0008212,Pechet factor deficiency,"['Dynia factor deficiency', 'Pechet factor deficiency']",,169200,,C1868545,,,,C566814,,,,
mondo:0008213,pectus excavatum,"['funnel chest', 'pectus excavatum', 'pectus excavatum (disease)']",,169300,,,,,,D005660,754.81,,,0000767
mondo:0008214,Pelger-Huet anomaly,"['ovoid neutrophil nuclei, developmental delay, epilepsy and skeletal abnormalities', 'PHA', 'Pelger Huet anomaly', 'Pelger-Huet anomaly', 'Pelger-Huet nuclear anomaly']",9631,169400,,C0030779,"['-0.562', '0.1763', '0.2041', '-0.3445', '0.2155', '-0.0727', '-0.1395', '0.2666', '-0.1342', '-0.1924', '-0.01514', '-0.0376', '0.2104', '-0.01707', '-0.003883', '-0.00658', '0.01384', '-0.04065', '-0.1908', '-0.2854', '0.2827', '-0.261', '0.3015', '0.1501', '0.55', '-0.1149', '-0.04553', '-0.11786', '-0.02983', '-0.1039', '0.2406', '0.235', '0.3057', '0.12195', '0.1202', '-0.0985', '-0.02971', '-0.11084', '0.0594', '-0.709', '-0.01371', '-0.0712', '0.003708', '-0.0794', '-0.44', '-0.5073', '-0.0851', '-0.08746', '0.3281', '-0.02122', '0.2355', '-0.2241', '-0.03976', '0.1628', '-0.2898', '-0.1493', '0.36', '-0.068', '-0.3015', '0.2288', '-0.02461', '0.03494', '0.0932', '-0.0425', '-0.003418', '-0.1257', '0.03812', '0.1785', '-0.2788', '0.12146', '-0.3367', '0.0378', '-0.1565', '0.2131', '0.06445', '0.02744', '0.2377', '0.1855', '-0.2515', '-0.1213', '-0.0731', '-0.0696', '0.347', '-0.00754', '-0.3628', '-0.01883', '0.1432', '0.2827', '0.003822', '0.109', '-0.06433', '0.2827', '-0.2052', '-0.01294', '0.5166', '0.374', '0.355', '-0.4727', '-0.06015', '0.248']",C85002,1001093,D010381,,,10029377,
mondo:0008215,adult-onset autosomal dominant demyelinating leukodystrophy,"['adult-onset autosomal dominant leukodystrophy', 'leukodystrophy, demyelinating, ADULT-onset, autosomal dominant', 'autosomal dominant leukodystrophy with autonomic disease', 'leukodystrophy, adult-onset, autosomal dominant', 'Pelizaeus-Merzbacher disease, autosomal dominant or late-onset type', 'adult-onset autosomal dominant demyelinating leukodystrophy', 'Pelizaeus-Merzbacher disease, autosomal dominant or late-onset type, formerly', 'ADLD', 'autosomal dominant adult-onset demyelinating leukodystrophy', 'autosomal-dominant or late-onset type Pelizaeus-Merzbacher disease', 'multiple sclerosis-like disorder']",0060785,169500,99027,,"['-0.4949', '0.09894', '-0.3027', '-0.2349', '-0.3547', '-0.3184', '-0.1113', '0.939', '-0.311', '-0.4138', '-0.02435', '-0.1595', '-0.4856', '-0.0501', '0.835', '0.1459', '-0.008804', '0.0832', '-0.2935', '-0.4749', '0.011665', '-0.4343', '0.000387', '0.00719', '0.2502', '0.10846', '-0.2291', '0.2239', '-0.9575', '-0.0356', '0.512', '-0.01639', '0.318', '-0.0477', '0.2473', '-0.07916', '-0.546', '-0.1126', '-0.03165', '0.1864', '-0.0814', '-0.1232', '0.08685', '0.197', '0.4456', '-0.4436', '0.05505', '0.2151', '-0.3926', '-0.1477', '0.41', '0.7656', '-0.3262', '-0.3464', '-0.4436', '0.1719', '0.6416', '-0.508', '-0.431', '-0.001541', '-0.0792', '-0.1252', '0.2505', '0.2196', '-0.524', '-0.2227', '0.04388', '0.2147', '-0.1284', '0.8438', '-0.1362', '0.0727', '-0.2', '0.057', '0.3193', '0.4297', '-0.12256', '0.647', '-0.2235', '-0.3472', '-0.00889', '-0.7617', '0.6523', '0.698', '0.328', '0.4504', '0.3386', '-0.10284', '0.583', '-0.1511', '0.331', '-0.1946', '-0.0393', '0.5396', '0.53', '0.3535', '0.699', '-0.1737', '0.729', '0.7046']",,,C566813,,,,
mondo:0008216,pelvic lipomatosis with crossed renal ectopia,['pelvic lipomatosis with crossed renal ectopia'],,169545,,C1868511,,,,C566812,,,,
mondo:0008217,pelvis-shoulder dysplasia,"['pelvis-shoulder dysplasia', 'Kosenow syndrome', 'Scapuloiliac dysostosis']",,169550,2839,C1868508,,,,C566811,,,,
mondo:0008218,Hailey-Hailey disease,"['familial benign chronic pemphigus', 'familial benign pemphigus', 'benign familial pemphigus', 'pemphigus, benign familial', 'Hailey-Hailey disease', 'benign chronic familial pemphigus of Hailey-Hailey', 'benign chronic pemphigus', 'BCPM']",0050429,169600,2841,C0085106,"['0.5864', '-0.2471', '-0.3542', '-0.5674', '-0.184', '-0.4814', '0.3098', '-0.1573', '-0.2429', '-0.3228', '0.10114', '-0.1322', '-0.3662', '0.3901', '-0.005444', '0.6533', '-0.1659', '-0.1946', '0.05624', '-0.56', '-0.333', '-0.1945', '0.4832', '-0.1849', '-0.4705', '0.03354', '0.1808', '0.0712', '-0.01958', '-0.2495', '0.406', '-0.231', '0.04465', '-0.08575', '-0.1814', '0.3713', '-0.38', '-0.1755', '0.2017', '0.0751', '0.1923', '-0.358', '0.591', '-0.1124', '0.724', '-0.1852', '-0.7803', '0.1559', '0.1225', '0.3982', '-0.1093', '-0.0937', '0.06494', '-0.0721', '0.1543', '0.29', '0.4062', '-0.1465', '-0.6216', '-0.2211', '0.03134', '0.3604', '-0.535', '-0.1305', '0.495', '0.0634', '0.971', '0.1738', '-0.02959', '0.719', '-0.2246', '-0.4717', '-0.2554', '-0.3657', '0.2285', '0.01241', '0.429', '0.0935', '-0.10333', '-0.4197', '-0.1547', '0.2795', '-0.02147', '0.045', '0.0721', '0.02725', '-0.0522', '0.2101', '-0.002592', '0.5264', '0.289', '0.0328', '-0.06', '0.1406', '0.5303', '-0.2607', '0.344', '-0.208', '-0.1729', '-0.09454']",C82865,,D016506,,,,
mondo:0008219,pemphigus vulgaris,"['pemphigus vulgaris, familial', 'familial pemphigus vulgaris']",0060851,169610,704,C0030809,,C34910,0004719,C536645,,L10.0,10052802,
mondo:0008221,prolidase deficiency,"['Imidodipeptidase deficiency', 'prolidase deficiency', 'Peptidase deficiency', 'hyperimidodipeptiduria']",0111540,170100,742,C0268532,"['0.1727', '0.0514', '-0.2732', '-0.1885', '0.2378', '-0.4187', '0.5317', '0.2308', '-0.2795', '-0.26', '0.02457', '0.649', '0.011345', '0.068', '-0.1818', '0.3828', '0.1056', '0.06525', '-0.305', '-0.4058', '-0.04797', '-0.3584', '0.6475', '-0.3345', '-0.5757', '-0.171', '-0.4087', '0.1208', '0.1826', '-0.8184', '0.6094', '-0.11884', '0.04742', '-0.206', '-0.1239', '-0.0801', '-0.6025', '-0.66', '0.1956', '0.07043', '-0.2097', '-0.335', '0.1538', '-0.3147', '0.1562', '0.4014', '0.3018', '0.344', '-0.0489', '-0.1821', '-0.716', '0.393', '0.1047', '0.1729', '-0.2184', '0.266', '0.2998', '-0.3188', '-0.259', '0.248', '-0.09845', '0.2563', '-0.4043', '-0.0953', '0.4211', '-0.4062', '0.3623', '0.7173', '0.1846', '0.4253', '-0.473', '-0.2974', '-0.213', '-0.006935', '-0.0493', '0.2083', '0.3616', '-0.7837', '0.2512', '-0.2537', '0.1326', '-0.0696', '0.010185', '0.6875', '0.1481', '0.4216', '0.0692', '-0.2698', '0.1614', '0.4868', '0.2098', '0.1903', '-0.05057', '-0.195', '0.835', '0.5474', '0.22', '-0.1301', '0.297', '-0.01888']",C85029,,D056732,,,,
mondo:0008222,Andersen-Tawil syndrome,"['Andersen syndrome', 'Potassium-sensitive cardiodysrhythmic type', 'LQT7', 'periodic paralysis, Potassium-sensitive cardiodysrhythmic type', 'cardiodysrhythmic potassium-sensitive periodic paralysis', 'long QT syndrome type 7', 'ATS', 'Andersen cardiodysrhythmic periodic paralysis', 'Andersen-Tawil syndrome', 'long QT syndrome 7', 'Potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features']",0050434,170390,37553,C1563715,"['-0.1887', '-0.1354', '0.2205', '0.1678', '-0.0924', '-0.179', '0.5283', '0.301', '-0.2388', '0.02257', '0.1315', '-0.05463', '0.319', '-0.2212', '-0.5747', '0.12195', '-0.1796', '-0.03845', '-0.1884', '-0.805', '0.431', '-0.0527', '0.2336', '0.1948', '0.3254', '-0.595', '0.06027', '-0.1857', '0.2957', '-0.387', '0.3176', '0.08356', '0.803', '-0.2964', '-0.11865', '-0.3945', '0.12415', '-0.2551', '-0.00523', '-0.325', '0.1356', '-0.4348', '0.3948', '0.1874', '0.2573', '0.02304', '-0.5957', '0.8228', '0.373', '0.4658', '-0.531', '-0.0952', '-0.0977', '0.3975', '-0.1907', '-0.591', '-0.5303', '-0.09955', '0.03111', '0.3252', '-0.05438', '0.09985', '-0.504', '-0.10406', '-0.03302', '0.3494', '0.1443', '0.5894', '-0.4387', '0.2373', '-0.646', '0.504', '0.3306', '0.1228', '-0.2107', '0.09143', '0.254', '-0.583', '-0.1671', '-0.322', '0.576', '-0.1028', '-0.3032', '0.3794', '-0.1299', '0.10925', '0.007282', '0.0777', '0.2357', '-0.1322', '-0.2817', '-0.2096', '0.10297', '0.06015', '0.397', '0.2347', '0.6357', '-0.157', '-0.09894', '0.2546']",C84559,,D050030,759.89,,,
mondo:0008223,hypokalemic periodic paralysis,"['hypokalemic familial periodic paralysis', 'familial hypokalemic periodic paralysis', 'Westphall disease', 'periodic hypokalemic paralysis', 'HOKPP', 'HypoPP', 'familial periodic paralysis (& [hypokalaemic])', 'hypokalemic periodic paralysis', 'HKPP', 'periodic paralysis I']",14452,,681,C0238358,"['-0.3984', '0.3633', '-0.552', '-0.08545', '-0.3628', '-0.0091', '0.6147', '0.6895', '-0.4932', '-0.05798', '-0.953', '-0.3362', '0.4429', '0.6353', '0.1902', '0.2399', '-0.606', '0.2109', '-0.4475', '-0.6875', '0.259', '-0.1604', '0.3408', '0.2732', '-0.4236', '-0.2886', '-0.1707', '-0.2627', '-0.65', '-0.1526', '-0.0166', '0.3357', '0.0766', '-0.2036', '-0.4355', '0.2842', '0.03976', '-0.0664', '-0.2188', '0.02545', '-0.4458', '-0.927', '0.3088', '0.1882', '0.06143', '-0.0665', '-0.5586', '0.3752', '0.87', '0.4792', '-0.639', '-0.3804', '0.475', '-0.3206', '0.04208', '0.0937', '0.1499', '-0.4553', '0.05984', '0.11646', '0.1597', '-0.01599', '0.01388', '0.02992', '-0.4724', '0.919', '0.4583', '0.3254', '-0.2465', '0.3835', '0.2727', '-0.1534', '0.3767', '0.1692', '0.814', '0.2915', '0.5244', '0.01146', '0.00901', '-0.0621', '0.527', '-0.5723', '0.6514', '-0.0981', '-0.05112', '0.6733', '-0.2089', '0.6016', '0.405', '-0.0948', '0.5513', '0.1659', '-0.537', '-0.0838', '-0.05383', '0.1935', '0.431', '-0.804', '-0.752', '0.02191']",C84775,,D020514,,,,
mondo:0008224,hyperkalemic periodic paralysis,"['adynamia episodica hereditaria with or without myotonia', 'sodium channel muscle disease', 'primary hyperPP', 'Gamstorp disease', 'familial hyperkalemic periodic paralysis', 'hyperkalemic periodic paralysis', 'hyperkalemic periodic paralysis, type 2', 'Gamstorp episodic adynamy', 'primary hyperkalemic periodic paralysis', 'hyperPP', 'adynamia episodica hereditaria', 'HYPP', 'hyperKPP', 'normokalemic periodic paralysis, potassium-sensitive', 'hyperkalemic PP', 'familial hyperkalemic periodic paralysis (disorder) [ambiguous]', 'familial hyperPP']",14451,170500,682,CN074266,"['-0.00398', '0.3098', '-0.4995', '-0.3281', '-0.03082', '0.1914', '0.31', '0.519', '-0.4358', '0.277', '-1.063', '0.3777', '0.5947', '0.2217', '0.004402', '0.335', '-0.514', '-0.1044', '-0.3606', '-1.021', '0.2004', '0.0941', '0.2076', '0.3765', '-0.3696', '0.1009', '-0.04984', '-0.10846', '-0.4304', '-0.1208', '0.1688', '0.8423', '0.2515', '0.06793', '-0.6035', '0.3535', '-0.1777', '0.1192', '0.2031', '-0.3103', '0.08624', '-0.8613', '0.4944', '-0.2722', '0.5137', '0.2012', '-0.1353', '0.4465', '0.649', '0.582', '-0.815', '-0.2175', '0.188', '-0.3699', '-0.0717', '-0.2396', '0.12054', '-0.2642', '0.1862', '-0.2825', '0.3218', '0.2472', '-0.0473', '-0.139', '0.2664', '0.8804', '0.4517', '0.4539', '-0.0249', '0.083', '0.213', '0.12146', '0.291', '-0.04083', '0.984', '0.8594', '0.443', '-0.05032', '0.1857', '-0.12463', '0.777', '-0.10626', '0.2441', '-0.1006', '-0.01341', '0.298', '-0.1674', '0.3513', '0.4011', '-0.2314', '0.4182', '0.08295', '-0.2722', '0.5054', '0.534', '0.05435', '0.3564', '-0.3057', '-0.7925', '-0.2844']",C123429,,D020513,,,,
mondo:0008225,normokalemic periodic paralysis,"['NormoKPP', 'normokalemic periodic paralysis', 'normokalemic PP', 'potassium-sensitive normokalemic periodic paralysis', 'periodic paralysis type 3']",,170600,680,C0268445,,C122791,,,,,,
mondo:0008226,"periodontitis, aggressive 1","['periodontitis, aggressive, 1', 'periodontitis 1, juvenile', 'periodontitis, aggressive, type 1', 'juvenile periodontitis', 'periodontitis, juvenile', 'periodontitis, prepubertal']",1474,170650,,C0031106,"['0.8438', '-0.268', '0.1781', '0.703', '0.28', '-0.347', '0.1849', '0.49', '-0.529', '0.674', '-0.1732', '-0.5195', '-0.3882', '0.4927', '-0.2573', '-0.1863', '-0.592', '0.587', '-0.3357', '-1.145', '0.04428', '-0.3877', '0.1603', '-0.5083', '0.2391', '-0.2258', '-1.049', '-0.2396', '-0.1089', '-0.342', '-0.3826', '0.5435', '0.02985', '0.2615', '0.6416', '0.8013', '-0.0997', '0.1489', '0.5664', '-0.9077', '-0.1572', '0.1797', '-0.8228', '-0.3552', '0.2598', '0.00971', '-0.001161', '-0.1927', '0.0522', '-0.2245', '0.10486', '0.05606', '0.5825', '0.08', '-0.1004', '-0.3943', '-0.678', '-0.3066', '-1.1875', '-0.8896', '0.09045', '0.05237', '-0.51', '-0.7715', '-0.269', '0.12036', '0.718', '0.0563', '0.4268', '1.253', '0.2247', '-0.2347', '0.519', '-0.914', '0.4724', '0.221', '-0.2144', '0.664', '-0.2416', '-0.583', '-0.819', '-0.0816', '-0.118', '0.1299', '0.602', '-0.288', '0.3018', '-0.1969', '0.7925', '0.3054', '0.3013', '0.1273', '0.327', '0.6562', '0.3447', '-0.257', '-0.436', '-1.018', '-0.3113', '-0.4062']",,0006342,D010520,523.5,,,
mondo:0008227,peripheral dysostosis,"['peripheral dysostosis', 'dysostosis peripheral']",,170700,1795,CN074256,,,,,,,,
mondo:0008228,pernicious anemia,"['pernicious anemia', 'anaemia pernicious', 'Addison-Biermer anaemia', 'Biermer anaemia', 'Addison-Biermer anemia', 'Addison^s anemia', 'acquired pernicious anemia', 'juvenile onset pernicious anaemia', 'Addison anaemia', 'Biermer disease', 'anemia pernicious', 'Biermer^s anaemia', 'Biermer anemia', 'Biermer^s anemia', 'intrinsic factor deficiency', 'juvenile onset pernicious anemia', 'acquired pernicious anaemia', 'Addison^s anaemia']",13381,170900,120,C0002892,,C2871,0005576,D000752,281.0,,,
mondo:0008229,"peroneal nerve, accessory deep","['accessory deep peroneal nerve', 'peroneal nerve, accessory deep']",,170980,,C1868426,,,,C536001,,,,
mondo:0008230,"peroxidase, salivary","['SAPX', 'peroxidase, salivary']",,170990,,,,,,,,,,
mondo:0008231,Peyronie disease,"['Peyronie^s fibromatosis', 'Peyronie disease', 'Peyronie^s disease', 'Induratio penis plastica']",8616,171000,2870,C0030848,,C3316,,,607.85,,,
mondo:0008232,"phagocytosis, plasma-related defect 1N","['phagocytosis, plasma-related defect type 1N', 'phagocytosis, plasma-RELATED defect IN']",,171100,,C1868402,,,,C566808,,,,
mondo:0008233,pheochromocytoma,"['phaeochromocytoma', 'pheochromocytoma', 'pheochromocytoma, susceptibility to']",0050771,171300,,,,,,D010673,,,,
mondo:0008234,multiple endocrine neoplasia type 2A,"['thyroid carcinoma, familial medullary', 'multiple endocrine neoplasia II', 'multiple endocrine neoplasia, type II', 'Sipple syndrome', 'MEN2A', 'multiple endocrine neoplasia type II', 'MEA type 2a', 'MEA type II', 'multiple endocrine adenomatosis type 2A', 'ptc syndrome', 'men type II', 'multiple endocrine neoplasia, type 2A', 'multiple endocrine neoplasia IIA', 'pheochromocytoma and amyloid-producing medullary thyroid carcinoma', 'pheochromocytoma and amyloid producing medullary thyroid carcinoma', 'multiple endocrine adenomatosis, type II', 'multiple endocrine adenomatosis type 2a', 'men-2A syndrome', 'multiple endocrine adenomatosis type II', 'men type 2a', 'multiple endocrine neoplasia, type IIA', 'multiple endocrine neoplasia type 2A', 'men 2A']",0050430,171400,247698,C1833921,"['0.07574', '0.4373', '-0.2717', '-0.176', '0.0482', '0.2083', '0.2507', '0.0863', '-0.2725', '-0.2491', '0.08356', '0.303', '-0.4023', '0.3752', '-0.03433', '-0.682', '-0.2617', '-0.4016', '-0.11755', '-0.3447', '-0.2654', '-0.3303', '0.618', '-0.5913', '0.6343', '0.2976', '-0.2435', '-0.0794', '0.4202', '-0.278', '0.3408', '-0.03336', '0.416', '-0.1187', '0.10986', '-0.3967', '-0.71', '0.01136', '-0.503', '0.4695', '0.1926', '-0.4983', '0.6064', '-0.4392', '0.5117', '-0.0483', '-0.2095', '0.1764', '0.427', '0.1786', '0.446', '0.3777', '0.2109', '-0.582', '-0.6533', '0.1519', '0.3179', '-0.4683', '-0.3362', '0.1859', '0.5127', '-0.03394', '0.0971', '-0.3635', '0.1497', '0.1469', '0.401', '0.3135', '-0.2754', '0.1344', '0.1982', '-0.4214', '0.4465', '-0.2288', '0.5454', '-0.1255', '-0.3682', '0.3833', '-0.3713', '-0.3865', '-0.2825', '-0.2595', '-0.2104', '-0.486', '-0.0929', '-0.2198', '0.3054', '-0.2761', '0.5244', '-0.163', '0.09924', '0.2837', '0.6865', '-0.05832', '0.807', '-0.04956', '-0.0561', '-0.442', '-0.3005', '0.262']",C3226,,D018813,258.02,,,
mondo:0008235,pheochromocytoma-islet cell tumor syndrome,"['pheochromocytoma--islet cell tumor syndrome', 'pheochromocytoma--islet cell tumour syndrome', 'pheochromocytoma and islet cell tumor of the pancreas', 'pheochromocytoma-islet cell tumor syndrome', 'pheochromocytoma and islet cell tumour of the pancreas']",,171420,,C1868392,,,,C566807,,,,
mondo:0008236,phlebectasia of lips,['phlebectasia of lips'],,171450,,C1868391,,,,C566806,,,,
mondo:0008237,phocomelia-ectrodactyly-deafness-sinus arrhythmia syndrome,"['Stoll-LC)vy-Francfort syndrome', 'facioauriculoradial dysplasia', 'phocomelia ectrodactyly deafness sinus arrhythmia', 'Stoll-levy-Francfort syndrome', 'phocomelia-ectrodactyly, EAR malformation, deafness, and sinus arrhythmia', 'Stoll-Lévy-Francfort syndrome']",,171480,2878,C1868390,,,,C537498,,,,
mondo:0008238,"phosphatase, acid, of tissues","['Acp3--Alpha polypeptide', 'phosphatase, acid, of tissues', 'lysosomal acid phosphatase']",,171660,,,,,,,,,,
mondo:0008239,phosphoglucomutase 4,"['phosphoglucomutase 4', 'Pgm4', 'milk PGM', 'phosphoglucomutase type 4']",,172110,,,,,,,,,,
mondo:0008240,6-phosphogluconolactonase deficiency,"['6Pgl deficiency', '6-phosphogluconolactonase deficiency', 'Pgls deficiency']",,172150,,C1868355,,,,C566803,,,,
mondo:0008241,phosphoglycoprotein 1,"['phosphoglycoprotein type 1', 'PGP1', 'phosphoglycoprotein 1']",,172290,,,,,,,,,,
mondo:0008242,"photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction","['photomyoclonus, diabetes mellitus, deafness, nephropathy, and cerebral dysfunction', 'Herrmann syndrome', 'hereditary photomyoclonus associated with diabetes mellitus, deafness, nephropathy, and cerebral dysfunction']",,172500,,C1809475,,,,C538113,583.9,,,
mondo:0008243,Pick disease,"['lobar atrophy of the brain', 'Pick^s disease', 'lobar atrophy of brain', 'Pick disease', 'dementia in Pick^s disease', 'dementia with lobar atrophy and neuronal cytoplasmic inclusions', 'PICK disease of brain', 'Pick disease of the brain']",11870,172700,,C0236642,"['-0.12335', '0.2164', '0.3074', '0.0813', '0.04135', '-0.1381', '-0.03745', '-0.1195', '-0.1902', '-0.0654', '-0.2678', '-0.2952', '-0.2087', '0.008156', '0.1332', '-0.611', '-0.1183', '-0.0845', '-0.1328', '-0.4314', '0.2651', '-0.2593', '0.1823', '0.0433', '-0.1614', '-0.154', '-0.2129', '-0.1964', '-0.2087', '-0.1903', '0.0672', '0.1699', '0.2386', '-0.0495', '0.0238', '-0.06256', '-0.1886', '-0.0999', '-0.2123', '-0.432', '0.2903', '-0.349', '-0.00977', '0.1249', '-0.01904', '-0.414', '0.2021', '0.006508', '0.3625', '0.192', '0.2676', '0.10724', '0.02461', '0.02173', '0.09314', '-0.2294', '0.3518', '-0.0608', '-0.4636', '0.1398', '-0.05557', '-0.01134', '0.193', '-0.2074', '-0.11053', '-0.03186', '0.1644', '0.3', '-0.2206', '0.0175', '0.08417', '-0.0184', '0.1361', '-0.1277', '-0.1142', '0.3572', '0.2546', '0.235', '-0.5044', '-0.3682', '-0.0663', '-0.4343', '-0.1694', '0.3079', '-0.01399', '-0.08594', '-0.007744', '0.1711', '0.2935', '0.05954', '0.3003', '0.1676', '-0.359', '0.1576', '0.02641', '0.0922', '0.301', '0.0918', '0.1092', '0.1892']",C85008,0003096,D020774,331.11,G31.01,,
mondo:0008244,piebaldism,"['piebaldism', 'PBT', 'partial albinism', 'piebald trait']",3263,172800,2884,C0080024,"['-0.363', '0.04974', '-0.011375', '-0.1711', '0.5596', '-0.3372', '-0.2922', '-0.02565', '-0.4456', '-0.0773', '-0.02132', '-0.0986', '0.0479', '-0.1881', '-0.4768', '-0.0302', '0.4119', '0.09534', '-0.2317', '-0.2876', '-0.3206', '-0.1698', '0.474', '-0.1708', '-0.1814', '0.006943', '-0.09705', '0.2532', '-0.2028', '0.124', '0.2666', '-0.3938', '-0.0777', '-0.02216', '0.10895', '0.362', '-0.3184', '0.1958', '-0.03967', '-0.2145', '0.304', '-0.4412', '-0.153', '-0.2445', '0.005424', '-0.4746', '0.1315', '0.5117', '0.3804', '0.09454', '-0.249', '-0.1595', '0.1216', '0.0378', '-0.4639', '-0.2883', '0.2588', '0.05157', '-0.4243', '-0.3684', '-0.1935', '-0.0787', '-0.0791', '0.05618', '-0.01817', '0.2834', '0.4631', '0.3193', '-0.1248', '0.3394', '0.0529', '-0.03323', '-0.01468', '0.1893', '-0.07513', '0.252', '0.06134', '-0.3416', '-0.003439', '-0.41', '0.2158', '-0.4805', '0.4456', '0.1968', '0.02101', '-0.3582', '-0.225', '0.4163', '0.1517', '0.1763', '0.172', '0.1351', '0.1384', '0.252', '0.573', '0.1053', '0.082', '-0.2262', '0.08276', '0.23']",C85009,,D016116,270.2,E70.3,,
mondo:0008245,piebald trait-neurologic defects syndrome,"['piebald trait neurologic defects', 'piebald trait with neurologic defects', 'telfer Sugar Jaeger syndrome', 'telfer-Sugar-Jaeger syndrome', 'White forelock and leukoderma with neurological impairment']",,172850,2885,C1868311,,,,C536955,,,,
mondo:0008246,pigmented paravenous retinochoroidal atrophy,"['PPCRA', 'pigmented paravenous chorioretinal atrophy', 'PPRCA']",0111541,172870,251295,C1868310,"['-0.4473', '-0.02031', '0.0867', '-0.0868', '0.2103', '-0.362', '-0.361', '0.02396', '-0.4143', '-0.03108', '0.03427', '-0.04056', '-0.2161', '-0.1461', '-0.05188', '-0.3713', '0.3215', '-0.04175', '0.2866', '-0.5107', '-0.25', '-0.2805', '0.006516', '0.06396', '-0.18', '0.0831', '-0.2852', '-0.01208', '-0.1624', '-0.006474', '0.3218', '-0.0991', '0.2078', '0.0809', '-0.1276', '0.3413', '-0.1016', '0.04886', '0.1877', '-0.575', '0.533', '-0.35', '0.000958', '0.1746', '-0.0768', '-0.1097', '-0.1321', '0.1748', '0.0342', '0.0844', '0.3528', '0.297', '0.06903', '-0.206', '-0.1011', '-0.1527', '0.5806', '-0.2006', '-0.541', '-0.01299', '0.01193', '-0.10077', '0.02483', '0.1643', '-0.311', '0.02596', '0.641', '0.517', '0.10065', '0.3267', '-0.255', '0.0663', '0.362', '-0.0009117', '0.225', '-0.163', '0.0671', '0.0641', '-0.06805', '-0.3936', '0.09033', '-0.3684', '0.0772', '0.5215', '-0.10254', '-0.237', '-0.1273', '0.006763', '0.07153', '0.1056', '0.3132', '0.4067', '0.2228', '0.1793', '0.533', '0.123', '0.415', '-0.2375', '0.04654', '0.2421']",,,C566801,,H35.5,,
mondo:0008247,Robin sequence-oligodactyly syndrome,"['Robin sequence and oligodactyly', 'Pierre Robin syndrome and oligodactyly', 'Pierre Robin sequence-oligodactyly syndrome']",,172880,3104,C1868309,,,,C535688,,,,
mondo:0008248,pigmented purpuric eruption,"['progressive pigmented purpura', 'pigmented purpuric dermatosis', 'pigmented purpuric eruption', 'pigmented purpura', 'familial pigmented purpuric eruption', 'Schamberg disease', 'Schamberg purpura']",,172900,,C0406515,,,,C537186,,,,
mondo:0008249,pilonidal sinus,"['pilonidal sinus (disease)', 'pilonidal sinus']",,173000,,,,,,D010864,,,,0010769
mondo:0008250,isolated growth hormone deficiency type II,"['IGHD 2', 'autosomal dominant pituitary dwarfism due to isolated growth hormone deficiency', 'autosomal dominant isolated growth hormone deficiency', 'Growth hormone deficiency, isolated autosomal dominant', 'IGHD II', 'congenital isolated GH deficiency type II', 'Growth hormone deficiency, isolated, autosomal dominant', 'isolated growth hormone deficiency, type II', 'congenital isolated growth hormone deficiency type II', 'pituitary dwarfism due to isolated Growth hormone deficiency, autosomal dominant', 'growth hormone deficiency, isolated, type II', 'isolated growth hormone deficiency type 2', 'isolated Growth hormone deficiency, type 2', 'IGHD2', 'congenital IGHD type II', 'pituitary dwarfism due to isolated growth hormone deficiency autosomal dominant']",0060872,173100,231679,C0271567,"['-0.3293', '0.1247', '-0.2397', '-0.1063', '0.1387', '0.2795', '0.4014', '-0.1576', '-0.1283', '-0.2325', '-0.04813', '-0.1906', '0.142', '0.295', '-0.4045', '-0.2585', '-0.0498', '-0.1136', '-0.2169', '-0.3403', '-0.08026', '-0.239', '0.3545', '-0.3948', '0.1116', '-0.10425', '-0.0451', '-0.1013', '0.02106', '-0.2465', '0.1464', '-0.05252', '0.2974', '-0.1522', '-0.012794', '-0.2072', '-0.08545', '0.02122', '-0.0796', '-0.2152', '0.09393', '0.1844', '0.02794', '-0.1725', '0.3228', '-0.2106', '0.2296', '-0.1084', '0.0794', '-0.03525', '0.1642', '-0.0753', '0.06903', '0.2283', '-0.2285', '0.1294', '0.3848', '-0.2522', '-0.2854', '0.188', '0.0653', '0.1685', '-0.184', '0.02759', '-0.1469', '0.2932', '0.386', '0.3677', '-0.313', '0.0311', '-0.2284', '0.2036', '0.369', '-0.265', '0.04276', '0.264', '0.098', '0.0491', '-0.0335', '-0.1396', '-0.2327', '0.3567', '-0.1628', '-0.04642', '-0.1455', '-0.1477', '0.3591', '-0.05316', '0.4016', '-0.01659', '0.07947', '-0.002539', '0.0422', '-0.3196', '0.7544', '-0.00894', '0.1833', '-0.2795', '-0.1409', '0.3245']",,,C562704,,,,
mondo:0008251,familial pityriasis rubra pilaris,"['pityriasis rubra pilaris', 'PRP', 'hereditary pityriasis rubra pilaris', 'Devergie^s disease', 'pityriasis rubra pilaris--familial type']",,173200,2897,C2930842,"['-0.1663', '0.2365', '-0.3022', '-0.000598', '0.1409', '-0.4148', '-0.0488', '-0.292', '-0.4514', '0.2222', '0.2307', '0.2343', '-0.4644', '-0.2593', '0.0734', '-0.0782', '0.3914', '-0.129', '0.2773', '-0.665', '-0.155', '-0.05872', '0.58', '-0.3235', '0.2329', '0.1483', '-0.1522', '0.04153', '0.01828', '-0.1666', '0.49', '-0.04404', '0.0939', '0.2148', '0.2314', '0.361', '-0.2947', '-0.11786', '0.04456', '-0.04178', '0.1309', '-0.518', '0.06616', '-0.1996', '0.05005', '-0.1669', '-0.4333', '0.2512', '0.3293', '0.0774', '-0.0319', '0.153', '0.04297', '0.1724', '-0.448', '0.010414', '0.4722', '-0.2169', '-0.558', '-0.1581', '0.1752', '-0.04205', '-0.07733', '-0.1142', '0.4731', '-0.1421', '0.3242', '0.357', '0.2396', '0.6445', '-0.3208', '-0.4277', '0.3025', '-0.05008', '-0.187', '0.0883', '0.003363', '0.11163', '-0.01802', '-0.3218', '-0.08734', '-0.2102', '-0.3071', '-0.05762', '0.1465', '-0.1929', '-0.0682', '0.06134', '0.2395', '0.3372', '0.3464', '0.1663', '0.12164', '0.2888', '0.409', '0.1443', '0.4766', '-0.606', '0.144', '-0.07806']",,,C531784,696.4,,10035116,
mondo:0008252,platelet adenylate cyclase activity,['platelet adenylate cyclase activity'],,173395,,,,,,,,,,
mondo:0008253,"platelet aggregation, spontaneous","['platelet aggregation, spontaneous']",,173400,,C1868263,,,,C566800,,,,
mondo:0008254,"platelet disorder, undefined","['platelet disorder, undefined']",,173420,,C1868258,,,,C566799,,,,
mondo:0008255,platelet factor 3 deficiency,['platelet factor 3 deficiency'],,173450,,C1868256,,,,C566798,,,,
mondo:0008256,platelet membrane fluidity,"['platelet membrane fluidity', 'PMF']",,173560,,,,,,,,,,
mondo:0008257,"platelet responsiveness to adrenaline, depressed","['platelet responsiveness to adrenaline, depressed']",,173580,,,,,,,,,,
mondo:0008258,platelet signal processing defect,['platelet signal processing defect'],,173590,,C1868199,,,,C566796,,,,
mondo:0008259,familial spontaneous pneumothorax,"['spontaneous pneumothorax', 'pneumothorax, primary spontaneous', 'Psp', 'primary spontaneous pneumothorax']",0080218,173600,2903,C4275252,"['0.3071', '-0.02542', '-0.912', '0.528', '-0.4941', '-0.11487', '0.619', '0.3872', '-0.8223', '-0.2319', '0.324', '-0.3496', '-0.3767', '0.0547', '-0.2966', '-0.0758', '-0.1009', '-0.00816', '-0.05005', '-0.9297', '-0.06183', '0.5405', '0.2465', '-0.298', '-0.1195', '-0.1041', '0.1866', '0.4248', '0.4534', '0.5024', '0.0839', '-0.6733', '0.5586', '0.2815', '0.04724', '0.1608', '-0.2576', '-0.3662', '0.03072', '0.22', '0.1483', '0.3047', '-0.1934', '-0.2236', '-0.2593', '0.3962', '-0.5674', '0.2203', '0.12146', '0.4028', '-0.513', '-0.10767', '0.212', '-0.2256', '0.2803', '-0.00755', '-0.752', '0.5996', '-0.6196', '-0.10175', '0.5117', '0.1914', '-0.2338', '0.171', '-0.12396', '0.05975', '0.5586', '0.3464', '-0.4468', '0.9443', '0.03345', '-0.263', '0.1814', '0.1731', '0.1957', '0.194', '0.544', '0.5615', '-0.1989', '-0.2059', '-0.5874', '-0.2255', '-0.4072', '0.1635', '0.07886', '-0.2742', '0.561', '0.9126', '0.0797', '-0.3787', '-0.266', '-0.4', '-0.6016', '0.647', '0.367', '0.09485', '0.2996', '-0.3572', '-0.919', '-0.1936']",,,C566795,,,,
mondo:0008260,Kindler syndrome,"['KS', 'KINDLER syndrome', 'KNDLRS', 'poikiloderma of Kindler', 'poikiloderma, congenital, with bullae, Weary type', 'congenital bullous poikiloderma', 'bullous acrokeratotic poikiloderma of Kindler and Weary', 'poikiloderma, hereditary acrokeratotic', 'Kindler syndrome']",0060472,173650,2908,,"['0.4917', '-0.2263', '-0.3867', '-0.1403', '-0.02884', '-0.3784', '-0.04608', '0.5894', '-0.5645', '0.12115', '-0.1395', '0.1278', '-0.789', '-0.0912', '-0.4214', '-0.12494', '0.4292', '-0.7197', '-0.1353', '-0.846', '-0.2272', '-0.4797', '0.2747', '-0.06046', '-0.1676', '0.6284', '-0.3171', '0.3555', '-0.4976', '-0.3784', '-0.03915', '-0.313', '0.01496', '0.1365', '0.3794', '0.11554', '-0.4092', '-0.263', '-0.12244', '0.2063', '0.1324', '0.1432', '0.2952', '0.12213', '0.176', '-0.0954', '-0.505', '0.368', '-0.9106', '-0.304', '-0.1494', '-0.3267', '0.502', '0.21', '-0.6147', '-0.283', '0.4626', '0.597', '-0.491', '-0.296', '-0.1483', '0.2142', '-0.1472', '0.312', '0.4531', '0.3137', '0.503', '0.4238', '0.03152', '0.8555', '-0.2141', '-0.1562', '-0.03165', '0.4612', '0.4534', '-0.4155', '-0.4365', '-0.239', '0.1659', '-0.2089', '-0.2095', '-0.0664', '-0.317', '0.155', '-0.3142', '0.3884', '0.03802', '0.583', '0.756', '-0.8037', '-0.04282', '0.3538', '0.1105', '-0.05597', '0.256', '0.2166', '0.752', '0.02338', '0.2482', '-0.146']",,,C536321,,,,
mondo:0008261,"hereditary sclerosing poikiloderma, Weary type","['poikiloderma, hereditary sclerosing']",,173700,221039,,,,,C562824,,,,
mondo:0008262,Poland syndrome,"['Poland syndactyly', 'Poland^s syndactyly', 'pectoralis muscle, absence of', 'unilateral defect of pectoralis muscle and syndactyly of the hand', 'Poland syndrome', 'Poland^s syndrome', 'Poland anomaly', 'Poland sequence']",12961,173800,2911,C0032357,,C85017,,D011045,756.89,,10036007,
mondo:0008263,polycystic kidney disease 1,"['polycystic kidney disease, adult, type 1', 'PKD1', 'polycystic kidney disease, adult', 'PKD1 autosomal dominant polycystic kidney disease', 'APKD1', 'autosomal dominant polycystic kidney disease caused by mutation in PKD1', 'polycystic kidney disease 1', 'polycystic kidney disease type 1', 'polycystic kidney disease, adult, type I', 'polycystic kidney disease 1 with or without polycystic liver disease', 'Potter type 3 polycystic kidney disease, formerly', 'Potter type 3 polycystic kidney disease']",0110858,173900,,C3149841,,,,C536326,,,,
mondo:0008264,autosomal dominant medullary cystic kidney disease with or without hyperuricemia,"['medullary cystic disease', 'medullary cystic kidney disease', 'autosomal dominant interstitial kidney disease', 'autosomal dominant tubulointerstitial kidney disease', 'polycystic kidneys, medullary type', 'autosomal dominant medullary cystic kidney disease', 'MCKD', 'autosomal dominant medullary cystic kidney disease with or without hyperuricemia', 'ADTKD']",,,34149,CN536252,"['-0.0952', '0.2788', '-0.7456', '0.3567', '-0.3018', '-0.2656', '-0.6533', '1.063', '-0.51', '-0.4783', '0.1207', '-0.4849', '-0.3074', '0.3733', '0.1956', '0.3271', '0.2224', '0.3762', '0.2656', '-0.741', '-0.3508', '-0.351', '0.09607', '0.179', '0.668', '-0.2316', '0.06616', '0.4375', '-0.461', '0.255', '0.2761', '-0.4429', '0.359', '0.3315', '-0.13', '-0.6475', '-0.1708', '0.10706', '-0.3767', '-0.2842', '-0.1323', '0.2318', '0.3252', '-0.1478', '0.2034', '-0.295', '-0.1048', '-0.2428', '0.0355', '0.1131', '0.4597', '0.173', '0.0709', '-0.6836', '0.209', '-0.5527', '0.364', '-0.264', '-0.861', '0.3835', '0.685', '0.2491', '-0.1952', '-0.04306', '0.06647', '-0.63', '0.921', '-0.263', '-0.4248', '0.02469', '-0.529', '-0.603', '0.7334', '-0.001598', '1.256', '0.2147', '0.1488', '0.647', '-0.4854', '0.5693', '0.479', '-0.188', '0.4526', '-0.2357', '-0.297', '0.3403', '0.585', '-0.407', '-0.1113', '-0.0533', '0.3486', '0.3018', '-0.09', '-0.3723', '0.751', '0.4707', '0.0344', '-0.382', '-0.815', '0.1799']",,0008617,C536137,,,,
mondo:0008265,polycystic liver disease 1,"['ADPCLD', 'autosomal dominant polycystic liver disease', 'nonsyndromic congenital polycystic liver disease', 'PCLD', 'PCLD1', 'nonsyndromic polycystic liver disease (disease)', 'isolated polycystic liver disease', 'polycystic liver disease', 'isolated congenital polycystic liver disease', 'polycystic liver disease 1 with or without kidney cysts', 'isolated autosomal dominant polycystic liver disease']",,174050,,C4255088,,,,,,,10048834,
mondo:0008266,"polydactyly, postaxial, type A1","['polydactyly, postaxial, type A1', 'polydactyly, postaxial', 'PAPA1', 'polydactyly, postaxial, types A1 and B', 'postaxial polydactyly, type A', 'postaxial polydactyly, type B']",,174200,93335,C1868120,"['-0.1298', '-0.2279', '0.1389', '0.067', '0.11847', '-0.307', '-0.1516', '0.1126', '-0.2396', '-0.2698', '-0.3936', '0.09674', '-0.02672', '0.08484', '-0.2869', '-0.1121', '0.10425', '-0.509', '0.01942', '-0.5654', '-0.05243', '0.0815', '0.256', '-0.02287', '0.3213', '0.1465', '-0.2238', '0.171', '0.2457', '-0.2366', '0.0982', '-0.2817', '0.05646', '0.01563', '0.2256', '-0.2406', '0.145', '0.05048', '-0.1101', '-0.2903', '0.0682', '0.006973', '-0.004967', '0.0109', '0.0959', '-0.0771', '-0.11084', '0.396', '0.12244', '0.06213', '-0.1306', '-0.2925', '-0.0676', '0.02022', '-0.5034', '-0.2017', '0.02571', '-0.1757', '-0.346', '-0.09424', '0.1721', '0.0619', '-0.0939', '0.1187', '-0.2893', '0.085', '0.2107', '0.1686', '-0.2042', '0.02678', '-0.265', '0.1007', '0.3164', '-0.0598', '0.2334', '-0.002836', '0.01942', '0.0654', '-0.299', '-0.4583', '-0.2605', '-0.04684', '0.3071', '0.4531', '0.06573', '-0.1635', '-0.1991', '0.2659', '0.0596', '-0.1945', '-0.0981', '0.3472', '0.3787', '0.1508', '0.4578', '-0.2198', '0.3013', '-0.593', '0.0572', '0.2429']",,,,,,,
mondo:0008267,orofaciodigital syndrome V,"['oral facial digital syndrome type 5', 'polydactyly postaxial with median cleft of upper lip', 'orofaciodigital syndrome Thurston type', 'polydactyly, postaxial, with Median cleft of upper lip', 'polydactyly, postaxial, with median cleft of upper lip', 'OFD syndrome 5', 'Thurston syndrome', 'OFD5', 'orofaciodigital syndrome V', 'oral-Facial-digital syndrome, type 5', 'orofaciodigital syndrome type 5', 'orofaciodigital syndrome type V', 'orofaciodigital syndrome, Thurston type', 'oral facial digital syndrome 5', 'oral-facial-digital syndrome type 5', 'Ofds 5', 'orofaciodigital syndrome 5', 'oral-facial-digital syndrome 5']",0060375,174300,2919,C1868118,"['0.2527', '0.2151', '0.0924', '0.0749', '0.4111', '-0.5034', '-0.1669', '0.4143', '-0.1898', '-0.582', '-0.3564', '-0.432', '-0.04813', '-0.1355', '-0.03041', '0.485', '0.3328', '-0.2484', '-0.05862', '0.009026', '-0.0457', '-0.0739', '0.129', '-0.01854', '0.1873', '0.05997', '-0.361', '0.2998', '0.5566', '-0.522', '0.4575', '-0.3066', '-0.123', '0.3066', '0.273', '-0.4602', '-0.006264', '-0.4758', '-0.066', '0.0788', '0.0356', '-0.5547', '0.05737', '-0.1493', '0.1362', '-0.2177', '-0.1876', '0.623', '-0.442', '-0.372', '-0.3452', '-0.2683', '-0.4683', '-0.008194', '-0.218', '-0.4893', '0.245', '-0.3708', '-0.2793', '0.01736', '0.2437', '0.2443', '0.03009', '-0.054', '-0.10175', '-0.1937', '-0.1382', '0.4358', '-0.301', '0.4927', '-0.3665', '-0.1016', '0.1592', '0.03156', '0.4587', '0.7554', '-0.3638', '-0.05933', '-0.343', '-0.2305', '0.00764', '0.0206', '0.624', '0.5337', '-0.02248', '0.426', '-0.01595', '0.8003', '0.02628', '0.1439', '0.1902', '0.1827', '0.02667', '-0.1941', '1.048', '-0.10864', '0.434', '-0.875', '-0.1288', '0.1642']",,,C557819,,,,
mondo:0008268,polydactyly-myopia syndrome,"['postaxial polydactyly-progressive myopia syndrome', 'postaxial polydactyly with progressive myopia', 'Czeizel-Brooser syndrome', 'polydactyly, postaxial, with progressive myopia', 'Czeizel Brooser syndrome', 'polydactyly-myopia syndrome', 'PMS', 'polydactyly myopia syndrome']",,174310,2917,,,,,C536331,625.4,,,
mondo:0008269,polydactyly of a biphalangeal thumb,"['thenar hypoplasia', 'Fromont anomaly', 'polydactyly, preaxial type 1', 'preaxial polydactyly type 1', 'PPD1', 'preaxial polydactyly 1', 'polydactyly preaxial 1', 'thumb polydactyly', 'polydactyly, preaxial 1', 'polydactyly, preaxial I']",,174400,93339,,"['0.05527', '-0.01125', '-0.01987', '0.141', '0.4868', '-0.4316', '0.005257', '-0.1334', '-0.4587', '-0.4915', '-0.2578', '-0.0956', '-0.279', '0.4421', '-0.2512', '-0.03778', '-0.1221', '-0.461', '-0.0451', '-0.481', '-0.02773', '0.5527', '0.7236', '-0.03128', '0.5093', '0.2678', '-0.4607', '0.1998', '0.4187', '-0.05627', '-0.0755', '-0.5234', '-0.0459', '0.09', '0.2013', '-0.27', '-0.2512', '-0.05466', '-0.3384', '-0.2391', '0.1279', '-0.0674', '-0.0845', '-0.1584', '0.4485', '0.01088', '-0.507', '0.272', '0.3079', '0.1487', '-0.3284', '-0.119', '-0.259', '-0.3281', '-0.883', '-0.4165', '0.2018', '-0.2185', '-0.2225', '-0.1184', '0.0943', '0.05563', '0.0909', '0.5317', '-0.698', '-0.01148', '0.1637', '0.234', '-0.2091', '-0.11066', '0.3022', '0.2457', '0.6177', '-0.0681', '0.2478', '0.5728', '-0.0693', '0.02039', '-0.4104', '-0.6377', '0.000662', '-0.2305', '0.2172', '0.326', '0.1418', '0.0563', '-0.04263', '0.09454', '-0.05722', '-0.365', '-0.3296', '0.2073', '0.2903', '-0.02933', '0.96', '-0.0862', '0.1827', '-0.9897', '-0.11255', '0.1768']",,,C536332,,,,
mondo:0008270,polydactyly of a triphalangeal thumb,"['PPD2', 'triphalangeal thumb-polydactyly syndrome', 'triphalangeal thumb with polysyndactyly', 'triphalangeal thumb-polysyndactyly syndrome', 'preaxial polydactyly type 2', 'polydactyly, preaxial 2', 'TPT-PS syndrome', 'triphalangeal thumb', 'polydactyly of triphalangeal thumb', 'polydactyly, preaxial type II', 'triphalangeal thumb, type i', 'polydactyly, preaxial II', 'polydactyly, preaxial type 2']",,174500,93336,C1868114,"['-0.2168', '0.3574', '-0.03616', '-0.2898', '0.378', '-0.2644', '-0.04962', '-0.5156', '-0.324', '-0.5444', '-0.2338', '-0.142', '-0.1781', '0.4512', '-0.285', '-0.4421', '0.1232', '-0.8013', '-0.02103', '-0.8496', '0.3577', '0.42', '0.6333', '-0.334', '0.934', '0.554', '-0.251', '0.011116', '0.762', '-0.08044', '-0.26', '-0.4282', '0.02792', '0.278', '0.5317', '-0.2166', '-0.7246', '-0.3489', '-0.8354', '-0.3884', '0.3118', '0.095', '0.1307', '-0.3828', '0.755', '-0.791', '-0.03287', '0.3806', '0.1859', '-0.09906', '-0.289', '0.2961', '0.04144', '-0.02278', '-0.4944', '-0.7095', '-0.04044', '0.03513', '-0.666', '0.2307', '0.1876', '-0.1453', '0.0598', '0.08307', '-0.3125', '-0.1099', '0.12256', '-0.05734', '0.02165', '0.271', '-0.1782', '0.06024', '0.542', '-0.01012', '0.2194', '0.296', '0.001618', '-0.29', '-0.4', '-0.8125', '0.01553', '-0.03442', '0.2139', '-0.00746', '0.2454', '-0.2307', '0.2239', '0.3994', '0.2139', '0.182', '-0.1434', '-0.1741', '0.6377', '-0.1555', '0.4646', '0.4902', '0.3574', '-0.7905', '-0.1277', '0.1288']",,,,,,,
mondo:0008271,polydactyly of an index finger,"['polydactyly, preaxial 3', 'preaxial polydactyly type 3', 'polydactyly, preaxial III', 'PPD3', 'index finger polydactyly', 'polydactyly, preaxial type 3']",,174600,93337,C1868113,,,,C566784,,,,
mondo:0008272,polysyndactyly 4,"['polydactyly, preaxial IV', 'polydactyly, preaxial 4', 'preaxial polydactyly type 4', 'polydactyly preaxial 4', 'preaxial polydactyly 4', 'crossed polydactyly type 1', 'polydactyly, preaxial, type IV', 'polysyndactyly, uncomplicated', 'crossed polydactyly, type 1', 'polysyndactyly uncomplicated', 'PPD4', 'polydactyly, preaxial type 4']",,174700,93338,C1868111,"['-0.331', '-0.0895', '0.3206', '-0.145', '0.1838', '-0.2322', '-0.1556', '0.1364', '-0.3716', '-0.3787', '-0.3872', '0.014145', '-0.11676', '-0.005753', '-0.2424', '-0.234', '0.317', '-0.5537', '-0.0997', '-0.7803', '0.05008', '0.3286', '0.6494', '-0.1583', '0.4968', '0.1995', '-0.1076', '0.255', '0.4448', '-0.506', '0.0734', '-0.372', '-0.00872', '0.2698', '0.3389', '-0.3435', '-0.1674', '-0.05905', '-0.2252', '-0.2551', '0.2034', '-0.3262', '0.3135', '-0.2197', '0.3303', '-0.2163', '-0.301', '0.376', '0.2052', '0.1892', '-0.2998', '-0.426', '-0.2805', '-0.2454', '-0.549', '-0.429', '0.09174', '-0.3933', '-0.3433', '0.255', '0.10004', '-0.1001', '0.11536', '0.1781', '-0.2617', '0.1489', '0.15', '0.2026', '-0.326', '0.0269', '-0.06107', '0.003319', '0.367', '-0.0174', '0.1886', '0.2449', '0.0849', '-0.0749', '-0.325', '-0.584', '-0.0968', '-0.1722', '0.3003', '0.6113', '0.2883', '-0.008995', '-0.4016', '0.3635', '-0.05194', '-0.3337', '-0.07495', '0.2317', '0.529', '0.11115', '0.638', '-0.278', '0.37', '-0.965', '0.0891', '0.3042']",,,,755.10,,10063143,
mondo:0008273,actinic prurigo,"['hydroa aestivale', 'familial polymorphous light eruption of American Indians', 'actinic prurigo', 'Hutchinson summer prurigo', 'polymorphic Light eruption, hereditary', 'juvenile Spring eruption of ears', 'hereditary polymorphous light eruption of American Indians']",,174770,330061,C0406217,,,,C566780,,,,
mondo:0008274,polyostotic fibrous dysplasia,"['polyostotic fibrous dysplasia of bone', 'PFD', 'fibrous dysplasia of bone']",,,93276,,,C34610,,D005359,756.54,Q78.1,10036120,
mondo:0008275,familial expansile osteolysis,"['EOF', 'FEO', 'expansile osteolysis, familial', 'osteolysis, familial expansile', 'polyostotic osteolytic dysplasia, hereditary expansile', 'Mccabe disease', 'hereditary expansile polyostotic osteolytic dysplasia', 'familial expansile osteolysis', 'McCabe disease', 'HEPOD']",0111542,174810,85195,,"['-0.11066', '0.2401', '0.2607', '-0.169', '0.279', '-0.2065', '0.11176', '0.4895', '-0.1626', '0.3098', '-0.3462', '-0.01697', '-0.1749', '-0.08514', '0.03964', '-0.1042', '0.06366', '-0.0956', '-0.1344', '-0.376', '0.00911', '-0.02898', '0.434', '-0.1836', '0.2091', '0.1604', '0.04633', '0.03055', '-0.275', '0.1145', '0.1598', '-0.1736', '-0.0224', '0.2344', '0.02243', '0.0383', '0.05554', '-0.2255', '-0.05856', '-0.4355', '0.0581', '-0.1772', '0.2415', '0.003183', '0.10455', '-0.4905', '-0.2925', '-0.047', '0.2015', '0.10693', '0.249', '0.1924', '0.488', '0.0743', '0.004547', '-0.4963', '0.1265', '-0.0483', '-0.1409', '-0.2361', '0.3542', '-0.1316', '-0.1989', '-0.3342', '-0.309', '0.08417', '0.4712', '0.5767', '0.2227', '0.2803', '-0.03314', '-0.2263', '0.08124', '-0.2747', '0.0913', '-0.143', '0.03983', '0.3672', '0.0812', '-0.3418', '-0.3457', '0.2235', '0.161', '0.3286', '-0.198', '-0.00292', '0.12024', '0.1957', '0.0667', '0.2463', '0.01855', '0.2878', '-0.1257', '0.3416', '0.366', '-0.02452', '0.7495', '-0.3433', '0.245', '0.0675']",,,C536335,756.9,,,
mondo:0008276,generalized juvenile polyposis/juvenile polyposis coli,"['juvenile polyposis syndrome', 'jPS', 'polyposis, juvenile intestinal', 'juvenile polyposis of stomach', 'polyposis, familial, of Entire gastrointestinal tract', 'juvenile intestinal polyposis', 'juvenile polyposis coli']",0050787,,329971,CN204230,"['0.014015', '0.1367', '-0.02373', '-0.0315', '0.00718', '-0.1498', '0.0225', '0.1204', '-0.0783', '-0.0014', '-0.0764', '-0.003744', '-0.07654', '-0.01447', '-0.0525', '-0.12177', '-0.014824', '-0.07587', '0.00404', '-0.161', '-0.00693', '-0.01275', '0.1387', '-0.11755', '0.03305', '0.00807', '0.02573', '-0.03146', '-0.02696', '-0.0674', '0.0903', '-0.0484', '0.1046', '0.005783', '0.10986', '0.01721', '-0.10974', '-0.05655', '-0.0632', '-0.06152', '0.06018', '-0.1884', '0.0356', '-0.0301', '0.03845', '-0.01097', '-0.0715', '0.1003', '0.001897', '0.0718', '-0.02353', '0.02988', '0.01261', '0.00212', '-0.0669', '-0.10657', '0.05127', '-0.0305', '-0.1699', '-0.02155', '0.1257', '0.063', '0.01706', '0.0384', '0.08325', '0.0668', '0.1807', '0.04602', '-0.0939', '0.1525', '-0.03824', '-0.0594', '0.05026', '-0.03366', '-0.02895', '0.05908', '0.08405', '0.02415', '-0.03455', '-0.0794', '-0.02258', '0.01712', '-0.06885', '0.0769', '-0.02007', '0.00605', '0.09174', '0.0757', '0.1207', '0.0002133', '0.05344', '0.1111', '0.004787', '0.02144', '0.2092', '0.036', '0.1583', '-0.1436', '-0.10266', '0.015175']",,,,,,,
mondo:0008277,stomach polyp,"['polyps of stomach', 'gastric polyposis', 'gastric polyp', 'gastric polyposa', 'polyps of the stomach']",,,,C0236048,,C3954,,C562464,,,,
mondo:0008278,juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome,"['polyposis, generalized juvenile, with pulmonary arteriovenous malformation', 'telangiectasia, hereditary hemorrhagic, with juvenile polyposis coli', 'jPS/Hht', 'JP/Hht syndrome', 'polyposis, generalised juvenile, with pulmonary arteriovenous malformation', 'juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome', 'juvenile polyposis with hereditary hemorrhagic telangiectasia', 'JPHT']",0111543,175050,,C1832942,"['-0.01628', '0.04462', '0.007713', '-0.05798', '0.01002', '-0.1248', '0.0318', '0.03824', '-0.046', '-0.04135', '-0.04095', '0.04413', '-0.04028', '-0.04596', '0.014046', '-0.05634', '0.03436', '-0.0075', '-0.03653', '-0.1802', '-0.03064', '-0.02377', '0.10504', '-0.05832', '-0.0032', '-0.0094', '-0.0555', '0.02663', '-0.01814', '-0.08075', '0.03876', '-0.03075', '0.12067', '0.01134', '0.05988', '-0.02249', '-0.0229', '-0.0487', '-0.00683', '-0.1206', '0.04163', '-0.10254', '0.04907', '-0.07947', '0.09735', '-0.1076', '-0.0859', '0.0955', '0.008514', '-0.03836', '-0.0267', '-0.003056', '0.04822', '0.03168', '-0.04007', '-0.06586', '0.07306', '-0.02162', '-0.124', '0.02325', '0.03326', '0.03195', '0.0409', '-0.01808', '0.0756', '-0.00855', '0.1024', '0.0777', '-0.09937', '0.1779', '-0.07355', '-0.01892', '0.03186', '-0.0007234', '0.06207', '-0.0453', '0.0413', '0.02808', '-0.0475', '-0.0387', '-0.02043', '-0.0359', '-0.0395', '0.09686', '0.01199', '-0.0518', '0.09595', '0.03784', '0.0965', '-0.04785', '0.03708', '0.1229', '0.02277', '0.01848', '0.2313', '0.1288', '0.1384', '-0.1495', '-0.0162', '0.02985']",,,C563412,,,,
mondo:0008280,Peutz-Jeghers syndrome,"['Peutz-Jeghers syndrome', 'Peutz-Jeghers polyp of small intestine', 'PJS', 'Peutz-Jeghers small bowel hamartoma', 'colonic hamartomatous polyp', 'gastric Peutz-Jeghers polyp', 'Peutz Jeghers polyposis', 'hamartomatous intestinal polyposis', 'lentiginosis, perioral', 'periorificial lentiginosis syndrome', 'polyposis, hamartomatous intestinal', 'polyps-and-Spots syndrome', 'Jeghers-Peutz syndrome', 'Peutz^s syndrome', 'polyps and spots syndrome', 'Peutz Jeghers colon polyp']",3852,175200,2869,C1333088,"['0.548', '0.03806', '-0.4822', '-0.3174', '0.7036', '-0.04922', '0.0853', '0.4773', '-1.003', '0.1461', '-0.2654', '0.4546', '-0.0733', '-0.1848', '-0.1755', '-0.05606', '0.2369', '0.06177', '-0.008675', '-0.08356', '-0.5513', '-0.8096', '0.1656', '-0.616', '0.4666', '0.02019', '0.3103', '0.5293', '0.1428', '-0.312', '1.066', '-0.7534', '-0.1018', '-0.2915', '-0.0342', '0.01715', '-0.606', '-0.3203', '0.4143', '0.2142', '0.293', '-0.453', '0.818', '-0.639', '0.03265', '-0.4377', '0.1465', '0.1617', '0.5835', '0.7856', '-0.3154', '-0.12244', '-0.6606', '-0.0962', '-0.2673', '1.025e-05', '0.1233', '0.2715', '-0.8735', '-0.01317', '0.3635', '0.463', '-0.1843', '0.1622', '-0.0741', '0.3955', '0.714', '0.3599', '-0.12164', '1.065', '0.2363', '-0.618', '0.03503', '-0.0788', '0.477', '-0.3691', '-0.1814', '-0.1423', '0.2279', '0.04623', '-0.0612', '-0.385', '0.559', '0.10004', '-0.07574', '-0.00881', '-0.0478', '-0.328', '0.02342', '-0.594', '-0.1302', '0.09076', '-0.689', '-0.4087', '0.5596', '-0.5083', '0.6987', '-0.3794', '-0.0232', '0.5654']",C4733,,D010580,759.6,,10034764,
mondo:0008281,"polyposis, intestinal, scattered and discrete","['polyposis, intestinal, scattered and discrete', 'polyps, scattered, discrete intestinal']",,175400,,C1868006,,,,,,,,
mondo:0008282,"polyposis, intestinal, with multiple exostoses","['polyposis, intestinal, with multiple exostoses']",,175450,,C1868005,,,,C566776,,,,
mondo:0008283,Cronkhite-Canada syndrome,"['Cronkhite-Canada syndrome', 'gastrointestinal polyposis-skin pigmentation-alopecia-fingernail changes syndrome', 'polyposis, skin pigmentation, alopecia, and fingernail changes', 'polyposis skin pigmentation alopecia fingernail changes', 'gastric Cronkhite Canada polyposis', 'gastrointestinal polyposis-ectodermal changes syndrome', 'Cronkhite-Canada disease']",6225,175500,2930,C0282207,,C7035,,D044483,,,10062907,
mondo:0008284,polyposis of gastric fundus without polyposis coli,"['fundic gland polyposis', 'polyposis of gastric fundus without polyposis coli']",,175505,,C1868001,,,,C566775,,,,
mondo:0008285,"polyps, multiple and recurrent inflammatory fibroid, gastrointestinal","['gastrointestinal stromal tumor/GIST-plus syndrome, somatic or familial', 'polyps, multiple and recurrent inflammatory fibroid, gastrointestinal']",,175510,,C1868000,,,,C566774,,,,
mondo:0008286,crossed polysyndactyly,"['polysyndactyly, crossed', 'crossed polydactyly']",,175690,2935,C1867999,,,,C566773,,,,
mondo:0008287,Greig cephalopolysyndactyly syndrome,"['Greig cephalosyndactyly syndrome', 'Greig cephalopolysyndactyly syndrome', 'Greig syndrome', 'polysyndactyly with peculiars skull shape', 'Greig^s syndrome', 'polysyndactyly with peculiar skull Shape', 'GCPS']",14761,175700,380,C0265306,"['-0.2617', '-0.2952', '0.02162', '-0.3755', '0.1594', '-0.2222', '0.07117', '0.1974', '-0.9023', '-0.2727', '0.00658', '0.0932', '0.402', '0.00952', '-0.10345', '0.1633', '0.4456', '-0.4438', '-0.1305', '-0.543', '-0.04306', '0.1456', '0.451', '-0.03287', '-0.013885', '0.02444', '-0.4688', '0.377', '0.4685', '-0.448', '0.1394', '-0.3406', '0.1954', '0.141', '0.1526', '0.0438', '-0.1088', '-0.2373', '0.11066', '-0.129', '0.3203', '-0.000847', '0.4673', '-0.2634', '0.5684', '-0.72', '0.4255', '0.3406', '0.1298', '-0.003536', '-0.2654', '0.10187', '-0.3997', '-0.4077', '-0.464', '-0.0959', '-0.065', '-0.0603', '-0.034', '-0.1942', '0.2922', '0.005257', '0.0381', '0.3496', '0.003868', '0.2126', '-0.06934', '0.1797', '-0.514', '-0.2185', '-0.7705', '0.1375', '0.3113', '0.2046', '0.3972', '0.2183', '0.4497', '-0.2947', '-0.3313', '-0.6543', '-0.103', '-0.06903', '-0.139', '0.9165', '0.01836', '0.2064', '0.18', '0.395', '-0.0796', '0.1302', '-0.08167', '0.1425', '0.2673', '-0.1713', '0.2686', '0.03748', '0.785', '-0.917', '0.628', '0.2703']",C35255,,C537300,,,10053878,
mondo:0008288,popliteal cyst,"['baker cyst', 'popliteal cyst']",,175750,,,,,,D011151,727.51,,,
mondo:0008289,brain small vessel disease 1 with or without ocular anomalies,"['BSVD1', 'hemiplegia, infantile, with porencephaly', 'BSVD', 'infantile hemiparesis', 'COL4A1-related brain small vessel disease with haemorrhage', 'autosomal dominant retinal arteriolar tortuosity, infantile hemiparesis, and leukencephalopathy', 'porencephaly caused by mutation in COL4A1', 'hemiplegia, infantile, with porencephaly porencephaly, type 1', 'brain small vessel disease with or without ocular anomalies', 'POREN1', 'brain small vessel disease with Axenfeld-Riegar anomaly', 'porencephaly 1', 'COL4A1-related familial vascular leukoencephalopathy', 'COL4A1 porencephaly', 'T1P', 'retinal arteriolar tortuosity, infantile hemiparesis, and leukoencephalopathy, autosomal dominant', 'ADT1P', 'brain small vessel disease with axenfeld-rieger anomaly', 'porencephaly type 1', 'brain small vessel disease with haemorrhage', 'COL4A1-related retinal arteriolar tortuosity-infantile hemiparesis-autosomal dominant leukoencephalopathy syndrome', 'COL4A1-related brain small vessel disease with hemorrhage', 'leukoencephalopathy with axenfeld-rieger anomaly', 'brain small vessel disease with hemorrhage', 'porencephaly, type 1, autosomal dominant']",0090125,607595,36383,CN032791,,,,C564372,,,,
mondo:0008290,"porokeratosis 1, Mibelli type","['porokeratosis 1, multiple types', 'POROK1', 'porokeratosis 1, MIBELLI type', 'porokeratosis of Mibelli']",,175800,,,,,,,,,,
mondo:0008291,porokeratosis plantaris palmaris et disseminata,"['porokeratosis, palmar, plantar, and disseminated', 'porokeratosis 2, palmar, plantar, and disseminated type', 'porokeratosis palmaris Et plantaris disseminata', 'palmar, plantar and disseminated porokeratosis', 'porokeratosis plantaris palmaris et disseminata', 'porokeratosis 2, palmar, plantar, and disseminated', 'porokeratosis, palmar, plantar, and disseminated, 1', 'POROK2']",,175850,737,,,,,,,,,
mondo:0008292,punctate palmoplantar keratoderma type 2,"['palmoplantar keratoderma, punctate type II', 'PPPP', 'type 2 punctate PPK', 'keratoderma palmoplantar, punctate type 2', 'punctate palmoplantar hyperkeratosis type 2', 'PPKP2', 'porokeratosis punctata palmaris Et plantaris', 'punctate palmoplantar keratoderma type II']",0080213,175860,79502,C1867982,,,,,,,,
mondo:0008293,"porokeratosis 3, disseminated superficial actinic type","['Dsap', 'porokeratosis, disseminated superficial actinic, 1', 'porokeratosis, disseminated superficial actinic 1', 'porokeratosis 3, disseminated superficial actinic type', 'porokeratosis 3, multiple types', 'DSAP1', 'POROK3']",,175900,,,,,,C536339,,,,
mondo:0008294,acute intermittent porphyria,"['porphyria, acute intermittent, Nonerythroid variant', 'porphyria, acute intermittent', 'porphyria, Chester type', 'porphyria, Swedish type', 'HMBS deficiency', 'hydroxymethylbilane synthase deficiency', 'AIP', 'porphobilinogen deaminase deficiency', 'pyrroloporphyria', 'AIP - acute intermittent porphyria', 'PBGD deficiency', 'UPS deficiency', 'uroporphyrinogen synthase deficiency', 'porphyria intermittent acute']",3890,176000,79276,C0162565,"['0.08466', '-0.3206', '-0.62', '-0.5093', '-0.2874', '-0.531', '0.0865', '-0.264', '-0.6055', '0.1459', '-0.447', '0.4348', '-0.03827', '1.135', '-0.879', '0.03314', '0.3542', '0.3032', '-0.3835', '-0.501', '-0.0766', '-0.2532', '-0.079', '-0.3647', '0.1407', '-0.4534', '-0.10614', '-0.2612', '0.2004', '-0.716', '-0.00977', '-0.1428', '0.6353', '-0.934', '-0.2764', '-0.7236', '-0.536', '0.04486', '-0.0784', '-0.2905', '0.1814', '-0.4246', '0.1425', '-0.3806', '-0.1914', '-0.384', '0.2362', '-0.4346', '0.8545', '0.3403', '-0.2467', '0.8403', '0.825', '0.0692', '-0.1307', '-0.2181', '0.0918', '-0.301', '-0.0014925', '-0.1812', '-0.05814', '-0.02582', '0.838', '0.09393', '-0.1608', '0.742', '-0.2417', '0.746', '0.433', '0.02185', '-0.52', '-0.04187', '0.1458', '-0.907', '0.3513', '0.7583', '0.557', '0.12494', '-0.1159', '-0.6514', '0.1884', '-0.525', '0.4866', '-0.2397', '0.714', '0.744', '1.154', '0.4043', '-0.1862', '0.07184', '0.836', '-0.2123', '-0.621', '0.2788', '0.394', '1.061', '-0.02977', '-0.5884', '0.2313', '0.2954']",C84536,,D017118,,,,
mondo:0008295,sporadic porphyria cutanea tarda,"['porphyria cutanea tarda, type I', 'PCT, type 1', 'PCT, ^sporadic^ type', 'acquired porphyria cutanea tarda', 'porphyria cutanea tarda type I', 'porphyria cutanea tarda, type 1']",,176090,443057,C1867968,,,,C566768,,,,
mondo:0008296,familial porphyria cutanea tarda,"['PCT', 'hereditary porphyria cutanea tarda', 'porphyria, hepatoerythropoietic', 'porphyria cutanea tarda type II', 'uroporphyrinogen decarboxylase deficiency', 'Urod deficiency', 'porphyria cutanea tarda, type 2', 'porphyria, Hepatocutaneous type', 'PCT, ^familial^ type', 'porphyria cutanea tarda, susceptibility to', 'porphyria cutanea tarda', 'PCT, type 2']",,176100,95159,C0268323,"['0.08527', '-0.1941', '-0.978', '-0.3394', '-0.0745', '-0.4248', '0.03342', '-0.241', '-0.593', '-0.1608', '-0.1674', '0.444', '-0.1558', '1.267', '-0.7295', '-0.0542', '0.4204', '0.219', '-0.2053', '-0.6753', '-0.331', '-0.1987', '0.1877', '-0.2898', '0.05322', '-0.8247', '-0.2203', '-0.1683', '0.58', '-0.6934', '-0.2487', '-0.5938', '0.5713', '-0.9', '-0.2003', '-0.4275', '-0.612', '-0.3105', '0.2507', '-0.265', '0.269', '-0.3894', '0.1079', '-0.3557', '-0.01941', '-0.4937', '0.416', '-0.2998', '1.09', '0.0932', '0.1119', '0.52', '1.01', '0.3508', '-0.01762', '-0.1674', '-0.02785', '0.1116', '-0.06995', '-0.578', '-0.04785', '-0.0963', '1.005', '-0.03983', '-0.1992', '0.5884', '-0.1531', '0.7124', '0.3801', '-0.0873', '-0.422', '-0.2437', '0.3254', '-0.633', '0.4521', '0.6875', '0.2078', '-0.00955', '0.1395', '-0.3057', '0.1971', '-0.5186', '0.05704', '-0.4995', '0.6045', '0.4524', '1.39', '0.574', '-0.0968', '0.3042', '0.825', '-0.1844', '-0.684', '0.4263', '0.524', '1.109', '-0.1669', '-0.9', '0.4578', '0.3457']",,,,,,,
mondo:0008297,variegate porphyria,"['PPOX deficiency', 'porphyria variegata, susceptibility to', 'porphyria variegata', 'Protocoproporphyria', 'variegate porphyria', 'porphyria variegate', 'protoporphyrinogen oxidase deficiency', 'porphyria, South African type', 'VP', 'variegate porphyria, homozygous variant']",4346,176200,79473,C0162532,"['0.3345', '-0.1108', '-0.8584', '-0.6357', '-0.09906', '-0.1746', '-0.02968', '-0.141', '-0.5444', '-0.0966', '-0.2827', '0.366', '-0.112', '1.301', '-0.7305', '0.0762', '0.05624', '0.2688', '-0.495', '-0.605', '-0.494', '-0.2615', '0.1643', '-0.1407', '-0.09094', '-0.4858', '-0.2666', '-0.1063', '0.3064', '-0.6436', '0.0739', '-0.6807', '0.3684', '-0.877', '-0.304', '-0.3818', '-0.5615', '-0.1378', '0.12036', '-0.3276', '0.3105', '-0.4072', '-0.03616', '-0.4268', '-0.0799', '-0.4507', '0.255', '-0.4417', '0.515', '0.4824', '-0.1547', '0.4136', '0.8667', '0.1345', '0.0708', '0.00181', '0.1665', '0.08105', '-0.2351', '-0.4692', '0.004177', '-0.1631', '0.9473', '0.007965', '-0.154', '0.724', '-0.01395', '0.843', '0.3772', '0.1213', '-0.353', '-0.0281', '0.3079', '-0.8047', '0.4724', '0.646', '0.3945', '-0.10767', '0.1445', '-0.5146', '0.2515', '-0.829', '0.0819', '-0.5566', '0.5605', '0.2173', '1.07', '0.364', '-0.074', '0.06726', '0.7515', '-0.2825', '-0.6777', '0.438', '0.4001', '1.133', '-0.1803', '-0.635', '0.2642', '0.1611']",C85219,,D046350,,,,
mondo:0008298,postaxial tetramelic oligodactyly,"['oligodactyly tetramelic postaxial', 'postaxial oligodactyly, tetramelic']",,176240,2730,C1867924,,,,C566767,,,,
mondo:0008299,posterior column ataxia,"['posterior column ataxia', 'Biemond ataxia']",,176250,,C1867923,,,,C536342,,,,
mondo:0008300,Prader-Willi syndrome,"['Willi-Prader syndrome', 'obesity, muscular hypotonia, intellectual disability, short stature, hypogonadotropic hypogonadism, and small hands and feet', 'obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet', 'Prader-Willi-Labhart syndrome', 'Prader-Labhart-Willi syndrome', 'Prader-Willi syndrome chromosome region', 'Prader Willi syndrome', 'Prader-Willi-like syndrome associated with chromosome 6', 'PWS', 'Prader-Willi syndrome']",11983,176270,739,C0032897,"['-0.1268', '0.197', '-0.03983', '0.159', '-0.0553', '-0.2722', '-0.372', '0.893', '-0.4363', '-0.4202', '-0.257', '-0.5005', '0.4253', '0.3862', '-0.4458', '-0.1675', '-0.2732', '0.3909', '-1.032', '-0.2805', '-0.09204', '0.1846', '0.534', '-0.1971', '0.2654', '0.05093', '0.1407', '-0.3428', '0.351', '-0.368', '0.6367', '-0.4302', '-0.1791', '0.6245', '-0.5083', '0.1866', '-0.01997', '0.0983', '-0.3472', '-0.2605', '0.7725', '0.535', '-0.2008', '-0.1134', '0.1274', '-0.6387', '0.3557', '0.1229', '0.03008', '0.3652', '-0.662', '0.1672', '-0.586', '0.003069', '0.07996', '-0.08276', '-0.3274', '0.5063', '0.355', '-0.2937', '-0.036', '0.6836', '-0.04272', '-0.4363', '-0.367', '0.2485', '-0.4585', '0.1451', '-0.1968', '0.475', '-0.04037', '-0.3357', '-0.01366', '-0.4934', '-0.02533', '-0.0932', '0.1459', '0.3433', '-0.1923', '-0.1835', '0.2676', '0.05225', '0.05966', '0.0921', '0.0649', '-0.04102', '0.261', '-0.2096', '1.055', '0.4224', '0.1918', '0.01605', '-0.802', '0.007137', '0.389', '-0.2546', '0.009415', '-0.71', '0.1509', '0.3152']",C75463,,D011218,759.81,,10036476,
mondo:0008301,Guttmacher syndrome,"['autosomal dominant preaxial deficiency, postaxial polydactyly, and hypospadias', 'preaxial deficiency, postaxial polydactyly, and hypospadias', 'Guttmacher syndrome', 'preaxial deficiency, postaxial polydactyly and hypospadias', 'preaxial deficiency-postaxial polydactyly-hypospadias syndrome']",0111544,176305,2957,C1867801,"['-0.338', '0.3914', '0.05423', '-0.3975', '0.3733', '-0.818', '-1.145', '0.4363', '-0.2542', '-1.09', '0.1239', '0.0094', '0.0108', '0.3083', '-0.0403', '0.0896', '0.4556', '-0.4756', '-0.2856', '-0.4639', '-0.26', '0.2034', '0.2277', '-0.236', '0.9053', '0.02191', '-0.3364', '0.3157', '0.612', '-0.7344', '0.3972', '-0.3408', '-0.3384', '0.1852', '0.1769', '-0.658', '0.1716', '-0.2424', '-0.141', '-0.3264', '0.0616', '-0.1804', '-0.0855', '-0.1068', '0.362', '-0.1736', '-0.2192', '0.299', '0.2742', '-0.0745', '-0.0001818', '-0.2445', '-0.6523', '0.006523', '-0.2683', '-0.8423', '0.1743', '-0.0892', '-0.3865', '0.5996', '0.0766', '0.0893', '0.2593', '0.752', '0.04404', '0.2261', '-0.3394', '0.0813', '-0.563', '0.3171', '-0.901', '0.002178', '0.2208', '-0.1519', '0.3193', '0.3618', '0.05817', '0.563', '-0.403', '-0.1043', '0.508', '0.5674', '0.3494', '-0.0558', '-0.1475', '-0.0831', '-0.2712', '0.7554', '0.1091', '-0.1774', '-0.7734', '0.4414', '0.02696', '-0.1418', '0.811', '0.0007915', '-0.1523', '-1.103', '0.201', '0.2676']",,,C538278,,,,
mondo:0008302,centra precocious puberty 1,"['KISS1R central precocious puberty', 'precocious puberty, central, type 1', 'precocious puberty, central, 1', 'CPPB1', 'central precocious puberty caused by mutation in KISS1R']",0112310,176400,,C3805879,,,,,,,,
mondo:0008303,familial male-limited precocious puberty,"['precocious puberty, male', 'pubertas praecox', 'testotoxicosis, familial', 'precocious puberty, male-limited', 'LHCGR peripheral precocious puberty', 'familial Testotoxicosis (subtype)', 'Leydig cell adenoma, somatic, with male-limited precocious puberty', 'leydig cell adenoma, somatic, with precocious puberty', 'familial gonadotropin-independent male-limited sexual precocity', 'testotoxicosis', 'precocious puberty, male limited', 'FMPP', 'male-limited precocious puberty', 'sexual precocity, familial, gonadotropin-independent']",0111545,176410,3000,C1504412,,,,,,,10063656,
mondo:0008304,premature chromatid separation trait,"['PCS', 'premature chromatid separation trait', 'total premature chromatid separation trait']",,176430,,C1864389,"['-0.04205', '0.06274', '0.02899', '-0.04028', '0.05136', '-0.08374', '-0.03812', '0.11176', '-0.04852', '-0.05246', '-0.03021', '-0.01126', '-0.01081', '0.01553', '-0.02861', '-0.0803', '-0.006054', '-0.01749', '-0.02806', '-0.1772', '-0.0742', '-0.01282', '0.1348', '-0.02951', '0.1213', '0.0114', '0.0093', '0.02855', '0.04724', '-0.0282', '0.08167', '-0.04538', '0.0865', '0.05887', '0.05933', '-0.03143', '-0.0154', '-0.05438', '-0.0005302', '-0.1835', '0.001629', '-0.086', '0.06088', '-0.04276', '0.01677', '-0.1384', '-0.0555', '0.02592', '0.05298', '0.03854', '0.01004', '-0.0812', '-0.0404', '0.04764', '-0.01517', '-0.05215', '0.1103', '-0.02663', '-0.1213', '0.02412', '0.06866', '0.0641', '-0.0614', '0.08167', '0.04614', '-0.005028', '0.135', '0.073', '-0.1293', '0.10126', '-0.1095', '0.03952', '0.0664', '-0.0929', '0.010025', '0.1042', '0.05463', '0.00535', '-0.073', '-0.1187', '-0.009', '0.0319', '-0.0404', '0.05124', '0.02933', '0.04764', '-0.01874', '0.1179', '0.10187', '-0.0277', '-0.04922', '0.1058', '-0.00897', '0.05057', '0.1808', '0.05502', '0.1237', '-0.1208', '-0.001767', '-0.00554']",,0009077,,,,,
mondo:0008305,Currarino triad,"['Scra1', 'Currarino triad', 'partial sacral agenesis with intact first sacral vertebra, presacral mass and anorectal malformation', 'Currarino syndrome', 'sacral agenesis syndrome', 'sacral agenesis, hereditary, with presacral Mass, anterior meningocele, and/or teratoma, and anorectal malformation', 'CURRARINO syndrome']",0111546,176450,1552,C1531773,"['-0.3936', '0.1936', '0.3997', '-0.3716', '0.2013', '-0.095', '0.0789', '0.0712', '-0.2465', '-0.2974', '-0.221', '0.0681', '-0.1516', '-0.1611', '-0.39', '-0.2185', '0.11334', '-0.4153', '0.02417', '-0.2764', '0.11127', '0.1249', '0.3894', '-0.07855', '0.09576', '0.1987', '-0.299', '-0.03598', '0.297', '-0.1716', '0.02756', '-0.12286', '0.2177', '0.072', '0.2935', '-0.281', '0.1458', '-0.2179', '-0.11707', '-0.3574', '-0.02965', '-0.1493', '0.2656', '-0.2551', '0.1049', '-0.2527', '0.04486', '0.3293', '0.146', '0.277', '-0.06854', '0.1183', '0.005703', '-0.2228', '-0.525', '-0.2651', '0.0372', '-0.04697', '-0.4797', '0.10754', '0.185', '0.1993', '-0.2244', '0.0707', '0.032', '-0.002853', '0.2986', '0.0405', '-0.1523', '0.02124', '-0.00468', '0.06433', '0.2415', '0.08325', '-0.02335', '-0.0858', '-0.02039', '-0.1244', '-0.2983', '-0.3464', '-0.08386', '0.03223', '0.2764', '0.218', '-0.0897', '-0.01388', '0.03757', '0.3655', '0.1895', '-0.1135', '-0.01069', '0.3713', '0.2927', '0.06805', '0.3901', '-0.2715', '0.4993', '-0.3699', '-0.00465', '0.1931']",,,C536221,759.89,,,
mondo:0008306,ABri amyloidosis,"['cerebral amyloid angiopathy, British type', 'presenile dementia with spastic ataxia', 'ABri amyloidosis', 'dementia familial British', 'cerebral amyloid angiopathy, ITM2B-related, type 1', 'familial British dementia', 'familial dementia, British type', 'cerebral amyloid angiopathy, ITM2B-RELATED, 1', 'dementia, familial British', 'Bri amyloidosis', 'ITM2B-related cerebral amyloid angiopathy 1', 'FBD']",0070029,176500,97345,C1867773,"['0.2622', '-0.6445', '-0.4824', '0.1071', '0.1725', '-0.5107', '-0.6865', '0.3862', '-1.375', '0.12305', '-0.1771', '-0.0672', '-0.917', '0.3145', '-0.2927', '-0.215', '0.1387', '-0.2593', '-0.128', '-0.64', '0.2091', '-0.02576', '0.1653', '0.0395', '-0.04257', '0.5615', '-0.4873', '-0.2482', '0.09344', '0.4055', '0.2688', '-0.3835', '0.836', '-0.907', '0.4197', '-0.6123', '-0.3396', '0.3027', '0.1627', '-0.08795', '0.1542', '-0.1454', '-0.4976', '0.7515', '0.3987', '-0.6807', '-0.3455', '0.3403', '0.2896', '0.6685', '-0.06107', '1.117', '0.1654', '-0.1913', '-0.05026', '-0.1788', '0.6626', '-0.07227', '-0.588', '-0.75', '-0.4675', '0.2844', '0.688', '-0.8525', '-0.007935', '-0.2491', '0.51', '0.973', '-0.8574', '0.361', '-0.3315', '0.2517', '-0.463', '-0.4434', '0.385', '0.549', '-0.2568', '1.296', '-0.4983', '-0.8154', '-0.2056', '-0.3816', '-0.1421', '-0.02086', '0.312', '-0.4626', '-0.2124', '-0.0271', '0.2634', '-0.07074', '0.4353', '-0.3901', '-0.2627', '-0.359', '0.5254', '0.4546', '-0.5947', '-0.0198', '0.3682', '-0.0399']",,,C538208,,,,
mondo:0008307,"presenile dementia, Kraepelin type","['catatonia of Kraepelin', 'Kraepelin disease', 'presenile dementia, Kraepelin type']",,176600,,C1867772,,,,C535273,,,,
mondo:0008308,"priapism, familial idiopathic","['priapism, familial idiopathic', 'familial idiopathic priapism']",,176620,,C1867771,,,,C531791,,,,
mondo:0008309,primary release disorder of platelets,"['bleeding disorder due to primary defects in platelet release mechanism', 'primary release disorder of platelets']",,176630,,C1867770,,,,C566759,,,,
mondo:0008310,Hutchinson-Gilford progeria syndrome,"['progeria syndrome, childhood-onset', 'Hutchinson Gilford progeria syndrome', 'premature senility syndrome', 'Hutchinson-Gilford progeria', 'Hutchinson Gilford syndrome', 'Hutchinson-Gilford progeria syndrome', 'HGPS', 'progeria', 'Hutchinson-Gilford disease']",3911,176670,740,CN236401,"['-0.0766', '0.2932', '0.12195', '0.2001', '0.3374', '-0.8574', '0.0927', '1.391', '-0.158', '-0.3948', '0.2281', '-0.0764', '0.314', '0.2585', '-0.3896', '0.332', '0.64', '0.02954', '-0.1666', '0.00399', '-0.1306', '-0.4524', '0.0938', '-0.287', '0.7134', '0.6504', '0.0896', '0.465', '0.3982', '0.0592', '0.511', '-0.1467', '0.157', '0.1891', '-0.05453', '0.6055', '-0.0766', '0.01111', '-0.05234', '-0.749', '0.2162', '0.0107', '-0.4368', '0.09296', '-0.0774', '-0.489', '0.09436', '-0.04044', '0.4675', '-0.3333', '-0.3372', '0.4033', '0.2124', '0.3823', '-0.3933', '-1.033', '-0.4968', '0.2195', '0.1105', '0.02773', '-0.4883', '0.1995', '0.07574', '-0.473', '-0.0856', '0.405', '0.391', '0.3948', '-0.535', '0.956', '-0.504', '0.499', '0.3828', '0.385', '-0.2546', '-0.1783', '-0.1732', '0.5034', '-0.11676', '-0.284', '-0.1819', '-0.06122', '-0.1683', '-0.3494', '-0.11224', '-0.03014', '0.4404', '-0.03537', '0.6', '0.371', '0.3218', '-0.002333', '0.227', '0.5796', '0.04642', '0.0234', '0.3103', '0.0455', '0.4883', '0.01794']",C34951,,,259.8,,10036794,
mondo:0008311,progeria-short stature-pigmented nevi syndrome,"['Mulvihill-Smith syndrome', 'progeroid short stature with pigmented nevi']",,176690,2959,C1261128,,,,C536422,759.89,,,
mondo:0008312,autosomal dominant prognathism,"['prognathism, mandibular', '^Hapsburg jaw^', 'Hapsburg jaw', 'Habsburg jaw', '^Habsburg jaw^', 'prognathism mandibular']",,176700,2964,CN203311,,,,D008313,,,,
mondo:0008313,"pelvic organ prolapse, susceptibility to","['pelvic organ prolapse, susceptibility to', 'vaginal prolapse', 'pelvic organ prolapse, susceptibility to, 1', 'prolapse of vagina and rectum', 'rectal prolapse']",,176780,,C0034888,,,,,,,,
mondo:0008314,"pronation-supination of the forearm, impairment of","['pronation-supination of the forearm, impairment of']",,176800,,C1867726,,,,C566757,,,,
mondo:0008315,prostate cancer,"['prostate gland cancer', 'malignant tumour of the prostate', 'malignant tumor of prostate', 'malignant neoplasm of prostate', 'malignant prostate gland neoplasm', 'cancer of prostate gland', 'prostatic neoplasm', 'malignant prostate tumour', 'malignant tumor of the prostate', 'prostate cancer, familial', 'hereditary prostate cancer', 'NGP - new growth of prostate', 'malignant neoplasm of prostate gland', 'tumour of the prostate', 'malignant neoplasm of the prostate', 'tumor of the prostate', 'malignant tumour of prostate', 'malignant prostate neoplasm', 'prostatic cancer', 'prostate neoplasm', 'malignant prostate tumor']",10283,,,C0376358,,C7378,,D011471,185,,,
mondo:0008316,"thrombophilia due to protein C deficiency, autosomal dominant","['thrombophilia due to PROTEIN C deficiency, autosomal dominant', 'THPH3', 'thrombophilia 3 due to protein C deficiency, autosomal dominant', 'Proc deficiency, autosomal dominant', 'Protein C deficiency, acquired', 'thrombophilia due to protein C deficiency, autosomal dominant', 'Protein C deficiency, autosomal dominant']",0111909,176860,,,,,,,,,,
mondo:0008317,proteolytic capacity of plasma,['proteolytic capacity of plasma'],,176900,,,,,,,,,,
mondo:0008318,Proteus syndrome,"['Wiedemann^s syndrome', 'gigantism, partial, of hands and feet, nevi, hemihypertrophy, and macrocephaly', 'partial gigantism of hands and feet, nevi, hemihypertrophy, macrocephaly', 'proteus syndrome, somatic', 'hemihypertrophy and macrocephaly', 'partial gigantism-nevi-hemihypertrophy-macrocephaly syndrome', 'Proteus syndrome', 'Elattoproteus syndrome']",13482,176920,744,C0085261,"['0.0627', '0.2585', '-0.5044', '-0.3733', '-0.08325', '-0.241', '0.4912', '0.666', '-0.03406', '-0.5615', '-0.4568', '-0.07214', '0.494', '0.3699', '0.10675', '0.6387', '-0.1892', '-0.279', '-0.218', '-0.3672', '0.2426', '-0.06995', '0.7456', '0.06647', '-0.0896', '-0.2369', '-0.5903', '0.3752', '0.6074', '0.06033', '0.8477', '-0.4292', '0.3086', '0.1279', '0.02159', '0.3164', '-0.2368', '-0.08826', '0.01039', '0.04443', '0.00543', '-0.5415', '0.4648', '0.05542', '0.6924', '0.04456', '-0.8354', '-0.04666', '-0.1103', '-0.5635', '-0.0668', '0.3047', '-0.005466', '0.198', '-1.004', '-0.11035', '0.03583', '0.2693', '-0.0563', '0.456', '0.684', '-0.03214', '-0.4624', '0.55', '-0.04587', '0.3816', '0.1688', '0.2445', '-0.571', '0.8203', '-0.1057', '-0.4043', '-0.07996', '0.05313', '0.0657', '-0.09607', '-0.1316', '0.1421', '-0.634', '-0.6123', '-0.86', '-0.4487', '0.10266', '-0.0693', '-0.503', '0.0586', '0.4387', '-0.0529', '-0.2295', '0.2957', '0.7056', '0.1818', '-0.685', '0.1536', '0.37', '-0.3403', '0.908', '-0.2563', '-0.1874', '0.4902']",C85032,,D016715,759.89,,,
mondo:0008319,"protoporphyria, erythropoietic, 1","['erythrohepatic protoporphyria', 'protoporphyria, erythropoietic, 1', 'ferrochelatase deficiency', 'EPP', 'erythropoietic protoporphyria', 'heme synthetase deficiency', 'EPP1', 'protoporphyria, erythropoietic']",,177000,79278,,"['0.0893', '-0.3616', '-1.079', '-0.10864', '0.0315', '-0.208', '-0.05917', '-0.4097', '-0.6167', '0.04312', '-0.3914', '0.4536', '0.03595', '1.122', '-0.579', '-0.05313', '0.383', '0.1725', '-0.0314', '-0.476', '-0.1964', '-0.506', '0.2864', '-0.3308', '0.1204', '-0.7456', '0.03967', '-0.2172', '0.1989', '-0.637', '0.1003', '-0.424', '0.53', '-0.623', '-0.1248', '-0.2522', '-0.4604', '-0.2428', '0.198', '-0.3975', '0.2203', '-0.2487', '0.2688', '-0.5024', '-0.2927', '-0.536', '0.3416', '-0.356', '0.5728', '0.291', '-0.0769', '0.4646', '0.8755', '0.2131', '0.04514', '-0.2379', '0.1516', '0.4207', '-0.06082', '-0.548', '0.1583', '-0.02155', '0.692', '-0.00806', '-0.3682', '0.5786', '-0.1398', '0.7915', '0.6147', '0.1265', '-0.5723', '0.1682', '0.395', '-0.7773', '0.2788', '0.2717', '0.444', '-0.2676', '0.3162', '-0.4146', '0.365', '-0.415', '-0.1985', '-0.5366', '0.4128', '0.4656', '0.78', '0.2908', '-0.1375', '0.1305', '0.874', '-0.3408', '-0.68', '0.255', '0.3586', '0.824', '-0.1078', '-0.9536', '0.10486', '0.33']",C84698,,,,,,
mondo:0008320,Protrusio acetabuli,"['Protrusio acetabuli (disease)', 'Protrusio acetabuli', 'PROTRUSIO acetabuli']",,177050,,,,,,,,,,0003179
mondo:0008321,"pruritus, hereditary localized","['pruritus, hereditary localized']",,177100,,C1867499,,,,C566754,,,,
mondo:0008322,pseudoachondroplasia,"['spondyloepiphyseal dysplasia, Pseudoachondroplastic', 'spondyloepiphyseal dysplasia, PSEUDOACHONDROPLASTIC', 'Pseudoachondroplastic dysplasia', 'Pseudoachondroplastic spondyloepiphyseal dysplasia syndrome', 'pseudoachondroplasia', 'Pseudoachondroplastic spondyloepiphyseal dysplasia', 'pseudoachondroplastic dysplasia', 'PSACH']",0080047,177170,750,C0410538,"['-0.3655', '0.2252', '0.0528', '-0.2708', '0.4683', '-0.714', '0.3977', '0.7246', '-0.78', '-0.5015', '-0.1609', '0.5356', '0.3713', '0.3232', '0.0946', '0.3071', '0.312', '-0.6924', '-0.4548', '-0.6475', '-0.546', '-0.1251', '0.6387', '-0.1096', '-0.3672', '0.04407', '0.0791', '0.3372', '-0.1914', '0.2632', '0.02798', '-0.1595', '-0.2189', '0.47', '-0.1975', '-0.1162', '-0.02328', '-0.7065', '0.3032', '0.1749', '-0.265', '-0.1016', '0.253', '0.6934', '0.2827', '-0.1948', '-0.071', '0.11957', '0.7773', '-0.323', '-0.224', '-0.2566', '0.03918', '0.2118', '0.573', '-0.7695', '0.1687', '0.0339', '-0.123', '-0.1459', '0.3418', '0.1103', '-0.3882', '0.3257', '0.1786', '0.6646', '0.373', '0.2089', '0.1387', '-0.02142', '-0.1611', '-0.0813', '-0.1825', '-0.0604', '0.3772', '0.311', '0.0988', '-0.01198', '-0.0968', '-0.3113', '-0.1731', '-0.2722', '-0.2537', '0.2507', '-0.03436', '0.3125', '0.0955', '0.02605', '0.5376', '0.1776', '-0.4338', '0.02695', '-0.3162', '0.13', '0.3337', '-0.2129', '0.705', '-0.623', '0.7256', '0.1708']",C118635,,C535819,756.9,,,
mondo:0008323,Liddle syndrome,"['Liddle syndrome', 'pseudoaldosteronism', 'pseudohyperaldosteronism type 1', 'Liddle^s syndrome', 'LIDLS']",0050477,,526,C0221043,"['-0.1549', '-0.3938', '-0.9087', '0.283', '-0.2145', '-0.2054', '-0.04105', '0.69', '-0.3557', '-0.2595', '-0.1339', '-0.1729', '0.3179', '-0.2185', '-0.3806', '-0.2048', '-0.0666', '0.2415', '0.0942', '-0.963', '0.433', '-0.4053', '0.6865', '-0.1893', '0.2869', '0.01382', '-0.01547', '-0.1931', '0.3755', '-0.4358', '0.743', '0.2233', '0.6206', '0.0996', '-0.4434', '-0.3079', '-0.0769', '-0.3274', '0.407', '-0.5234', '-0.02083', '-0.2445', '0.4863', '-0.3538', '0.204', '-0.01756', '-0.2688', '0.05072', '0.1085', '0.3132', '0.3545', '0.2725', '0.2284', '-0.349', '0.2262', '-0.0795', '0.5024', '-0.6133', '0.004192', '0.339', '-0.4536', '0.614', '0.09985', '-0.4243', '-0.4077', '0.395', '-0.1654', '0.5273', '-0.3774', '0.2189', '-0.722', '0.008156', '0.03415', '0.48', '0.4194', '-0.1088', '0.3237', '-0.2842', '-0.3567', '-0.2109', '0.3167', '0.409', '-0.0973', '0.2097', '0.2113', '0.6445', '0.2737', '-0.0676', '0.4094', '0.255', '-0.07324', '-0.2023', '-0.1893', '-0.1722', '0.543', '0.432', '0.4038', '-0.1189', '-0.9614', '0.0802']",C84827,,D056929,,,10052313,
mondo:0008324,pseudoarthrogryposis,"['hereditary congenital rigidity of elbows and knees', 'ankylosis at elbow and knee', 'pseudoarthrogryposis']",,177300,,C1867485,,,,C566753,,,,
mondo:0008325,Pseudoatrophoderma colli,['Pseudoatrophoderma colli'],,177350,,C0406561,,,,C562909,,,,
mondo:0008327,exfoliation syndrome,"['XFG', 'pseudoexfoliation syndrome', 'XFS', 'pseudoexfoliation glaucoma']",13641,,529819,C0206368,"['-0.5327', '0.1248', '0.10547', '0.03296', '0.426', '0.05035', '-0.2134', '-0.22', '-0.273', '0.03937', '-0.2275', '-0.2042', '-0.007458', '-0.1355', '-0.451', '-0.10315', '0.001119', '-0.2524', '0.265', '-0.565', '0.01027', '-0.05096', '0.273', '0.2146', '0.07007', '0.319', '-0.2065', '0.383', '0.03247', '0.3806', '0.2325', '0.1298', '0.01179', '-0.002829', '0.1709', '-0.02475', '0.09424', '0.06335', '0.2145', '-0.826', '0.1703', '-0.2979', '0.1743', '0.2146', '-0.2456', '-0.2397', '0.2218', '0.1573', '0.6436', '-0.0776', '0.1963', '-0.2123', '0.2102', '-0.0453', '-0.1036', '-0.3235', '0.721', '0.2013', '-0.5635', '-0.1256', '0.04944', '-0.0438', '-0.10175', '0.0843', '-0.01773', '-0.1345', '0.4636', '0.4666', '-0.1362', '0.1573', '-0.4463', '-0.1192', '0.1066', '0.005043', '-0.2128', '0.1737', '-0.0228', '0.3672', '-0.1365', '-0.2039', '-0.00786', '-0.06555', '-0.04028', '0.3145', '-0.328', '-0.1967', '-0.1562', '0.2922', '0.0301', '0.2103', '-0.01607', '0.3105', '0.02623', '0.0849', '0.718', '0.0365', '0.404', '-0.2793', '-0.11896', '0.1277']",C129025,0004235,D017889,365.52,,,
mondo:0008328,"glaucoma 1, open angle, P","['glaucoma 1, open angle, type P', 'glaucoma 1, open angle, P', 'GLC1P']",,177700,,C3888338,,,,C566748,,,,
mondo:0008329,autosomal dominant pseudohypoaldosteronism type 1,"['pseudohypoaldosteronism, type I, autosomal dominant', 'renal pseudohypoaldosteronism type 1', 'autosomal dominant PHA 1', 'PHA I, autosomal dominant', 'pseudohypoaldosteronism type 1, dominant', 'autosomal dominant pseudohypoaldosteronism type 1', 'renal PHA1', 'pseudohypoaldosteronism type 1 autosomal dominant', 'PHA1A', 'pseudohypoaldosteronism type i, autosomal dominant']",0060855,177735,171871,C1449842,"['-0.1866', '-0.0292', '-0.05847', '0.07526', '0.0632', '-0.4185', '-0.2054', '0.9897', '-0.3967', '-0.2166', '-0.448', '0.1685', '-0.03262', '0.622', '0.05386', '-0.09845', '0.3772', '-0.2279', '-0.0067', '-0.969', '0.2598', '-0.3076', '0.4062', '0.02821', '0.4902', '0.04214', '0.00941', '0.1097', '-0.2505', '-0.2054', '0.4983', '0.2837', '0.461', '0.4941', '-0.486', '0.1034', '-0.1267', '0.2279', '-0.2827', '0.2089', '0.1443', '-0.1475', '0.713', '-0.1454', '0.05795', '-0.4534', '-0.3657', '-0.249', '-0.008316', '0.4062', '0.006466', '0.02084', '-0.02962', '-0.627', '-0.2922', '0.002153', '0.3232', '-0.522', '-0.08795', '0.825', '0.1957', '0.3313', '0.0779', '-0.7437', '0.4905', '0.007206', '0.1394', '-0.0701', '0.1819', '-0.1499', '-0.703', '-0.128', '0.0973', '-0.04166', '0.010956', '-0.1748', '0.08203', '-0.05417', '-0.114', '0.1503', '0.2144', '0.659', '-0.1328', '-0.1654', '-0.348', '0.5356', '0.3289', '-0.2059', '0.599', '0.3396', '0.1399', '0.2654', '-0.4985', '-0.7197', '0.703', '0.3984', '-0.06024', '-0.5615', '-0.0921', '0.352']",C126810,,,,,,
mondo:0008330,pseudomonilethrix,['pseudomonilethrix'],,177750,,C0432346,,,,C562988,,,,
mondo:0008332,platelet-type von Willebrand disease,"['VWDP', 'von Willebrand disease platelet-type', 'BDPLT3', 'pseudo-von Willebrand disease type 2B', 'Von Willebrand disease, platelet type', 'platelet-type bleeding disorder 3', 'platelet type-von Willebrand disease', 'Von Willebrand disease, Platelet-type', 'PT-VWD', 'bleeding disorder, Platelet-type, 3', 'pseudo-von Willebrand disease', 'pseudo-VON WILLEBRAND disease', 'platelet-type von Willebrand disease']",0111056,177820,52530,,"['-0.4246', '0.498', '-0.408', '0.2252', '-0.224', '-0.09174', '-0.2915', '0.569', '-0.0841', '-0.907', '0.4834', '0.6724', '0.608', '0.902', '0.1573', '-0.4768', '0.1704', '0.4607', '-0.3967', '-0.4607', '-0.0642', '-0.7393', '0.871', '0.3904', '-0.1211', '-0.2927', '-0.363', '0.1328', '0.686', '0.2303', '0.6396', '-0.3147', '0.2622', '0.4072', '-0.04626', '-0.3787', '-0.5176', '-0.2605', '0.1365', '-0.3154', '0.5034', '0.07294', '0.1895', '-0.5903', '0.269', '-0.3198', '-0.588', '0.195', '0.3157', '-0.1802', '0.7534', '-0.02399', '0.2769', '-0.1245', '-0.2046', '-0.552', '-0.4817', '1.047', '-0.7197', '-0.0753', '-0.623', '-0.0843', '0.558', '-0.5703', '0.05893', '-0.06934', '-0.2815', '-0.5186', '-1.01', '0.546', '-0.1857', '0.03198', '-0.2078', '-0.838', '0.6074', '0.3655', '0.8486', '0.855', '0.389', '0.03546', '-0.655', '-0.4368', '0.878', '-0.4714', '-0.00634', '0.4263', '0.08344', '0.214', '0.258', '0.0685', '-0.4924', '0.2988', '-0.01073', '-0.0775', '1.107', '0.6167', '0.005707', '-1.018', '-0.531', '0.0822']",C131681,,C536458,,,,
mondo:0008333,"pseudoxanthoma elasticum, forme fruste","['pseudoxanthoma elasticum, heterozygous', 'pseudoxanthoma elasticum, forme fruste']",,177850,,,,,,,,,,
mondo:0008334,"psoriasis 1, susceptibility to","['PSORS1', 'susceptibility to psoriasis 1', 'psoriasis caused by mutation in HLA-C', 'HLA-C psoriasis', 'psoriasis susceptibility 1', 'psoriasis 1, susceptibility to']",0111286,177900,,,,,,,,,,
mondo:0008335,short stature-craniofacial anomalies-genital hypoplasia syndrome,"['pterygia intellectual disability facial dysmorphism', 'Haspeslagh-Fryns-Muelenaere syndrome', 'pterygia, intellectual disability and distinctive craniofacial features', 'Haspeslagh syndrome', 'pterygia, mental retardation, and distinctive craniofacial features', 'pterygia mental retardation facial dysmorphism', 'pterygia, intellectual disability, and distinctive craniofacial features', 'pterygia, mental retardation and distinctive craniofacial features']",,177980,2994,C1867443,,,,C535844,,,,
mondo:0008336,"pterygium colli, isolated","['pterygium colli, isolated']",,177990,,C1867442,,,,C566741,,,,
mondo:0008337,familial pterygium of the conjunctiva,"['pterygium of the conjunctiva and cornea', 'pterygium of conjunctiva and cornea']",,178000,2989,C1867441,,,,C566740,,H11.0,,
mondo:0008338,"contractures, pterygia, and spondylocarpotarsal fusion syndrome 1A","['distal arthrogryposis type 8', 'multiple pterygium syndrome, autosomal dominant', 'DA8', 'pterygium syndrome, multiple, autosomal dominant', 'contractures, pterygia, and spondylocarpostarsal fusion syndrome 1A', 'arthrogryposis, distal, type 8']",0081321,178110,65743,C1867440,"['-0.5513', '0.07056', '0.3416', '-0.4856', '0.4685', '-0.616', '-0.0633', '0.4395', '-0.8867', '-0.543', '0.0509', '0.2123', '-0.05646', '-0.1078', '-0.03476', '0.353', '0.276', '-0.04016', '-0.39', '-0.4612', '-0.013176', '0.0462', '0.2563', '-0.08057', '0.292', '0.3457', '-0.2576', '0.11566', '0.2225', '-0.1028', '0.1516', '-0.2708', '0.1896', '0.1317', '0.3254', '-0.414', '-0.02142', '-0.2141', '0.0802', '-0.1836', '-0.07623', '-0.415', '0.0654', '0.1255', '0.2151', '-0.2705', '-0.1971', '0.6284', '0.2076', '-0.0901', '-0.378', '-0.06714', '0.193', '0.136', '-0.4575', '-0.61', '-0.00715', '-0.04883', '-0.1803', '0.0798', '0.4832', '0.013016', '-0.3455', '0.1982', '-0.1523', '0.1807', '0.356', '0.433', '-0.1619', '0.2588', '-0.5', '-0.0766', '0.1741', '-0.1656', '-0.2474', '0.02075', '0.00973', '0.1852', '-0.4622', '-0.11163', '0.01573', '0.0327', '0.2495', '0.393', '-0.1484', '0.0912', '-0.1864', '0.565', '0.1262', '0.1456', '-0.03653', '0.1967', '0.337', '-0.02376', '0.5747', '-0.0309', '0.6445', '-0.4292', '0.3403', '0.1315']",,,C566739,,,,
mondo:0008339,antecubital pterygium syndrome,"['pterygium, antecubital', 'antecubital pterygium', 'pterygium antecubital']",,178200,2987,C1867439,,,,C566738,,,,
mondo:0008340,"ptosis, hereditary congenital, 1","['ptosis, hereditary congenital, 1', 'congenital eyelid ptosis', 'ptosis, congenital', 'ptosis, hereditary congenital 1', 'congenital ptosis', 'congenital ptosis (disease)', 'PTOS1']",0060261,178300,91411,,,C27049,,C566737,743.61,,10015996,0007970
mondo:0008341,ptosis-strabismus-ectopic pupils syndrome,"['ptosis strabismus ectopic pupils', 'ptosis, strabismus, and ectopic pupils', 'McPherson-Hall syndrome']",,178330,2999,C1867437,,,,C566736,,,,
mondo:0008342,pubic bone dysplasia,['pubic bone dysplasia'],,178350,,C1867436,,,,C566735,,,,
mondo:0008343,pulmonary atresia with ventricular septal defect,"['pulmonary valve atresia with ventricular septal defect', 'pulmonary atresia with ventricular septal defect']",,178370,1207,C0344976,,C99033,,C562833,,,,
mondo:0008344,"pulmonary edema of mountaineers, susceptibility to","['HAPH', 'pulmonary oedema of mountaineers', 'pulmonary edema of mountaineers, susceptibility to', 'high altitude pulmonary hypertension', 'pulmonary edema of mountaineers']",,178400,,,,,,C535833,993.2,,,
mondo:0008346,pulmonary hemosiderosis,"['brown lung', 'brown induration', 'idiopathic pulmonary hemosiderosis', 'pulmonary hemosiderosis', 'alveolar hypoventilation syndrome', 'siderosis', 'pulmonary siderosis']",12118,178550,99931,,,,,D012806,516.1,,,
mondo:0008347,idiopathic and/or familial pulmonary arterial hypertension,"['PPH1', 'pulmonary hypertension, primary, 1', 'pulmonary hypertension, primary, type 1', 'IFPAH']",,,422,CN205068,"['0.1497', '0.434', '0.163', '-0.149', '0.0852', '-0.8267', '0.3662', '0.346', '-0.01411', '-0.6406', '0.2676', '-0.6704', '-0.3005', '-0.0383', '-0.1764', '-0.806', '-0.2588', '-0.3467', '0.4534', '-0.3884', '0.03687', '-0.05508', '0.4487', '-0.6', '-0.005993', '0.894', '0.2402', '0.2122', '0.299', '-0.1766', '0.6074', '-0.0668', '0.646', '-0.3237', '0.0744', '-0.815', '-0.317', '-0.05536', '0.2323', '-0.5317', '0.588', '-0.407', '0.7617', '-0.04593', '0.08813', '0.5825', '0.2135', '0.1903', '0.2241', '0.03162', '-0.197', '0.07965', '0.1948', '-0.1888', '-0.2307', '0.06805', '0.3936', '0.05493', '-0.3135', '0.7764', '-0.013504', '0.2467', '0.306', '-0.2299', '0.02985', '-0.10077', '0.2198', '0.53', '-0.3403', '0.7114', '-0.2732', '-0.2273', '0.3406', '-0.1605', '0.09406', '0.766', '-0.37', '0.003447', '-0.4614', '0.1017', '0.1539', '0.6406', '0.0386', '-0.4795', '0.294', '0.3433', '0.63', '0.2347', '0.08246', '-0.2306', '0.2241', '-0.511', '-0.6865', '0.04898', '1.157', '-0.10846', '0.388', '-0.0673', '-0.517', '-0.4385']",,,,,,,
mondo:0008348,pulmonary nodular lymphoid hyperplasia,"['pulmonary nodular lymphoid hyperplasia, familial', 'pulmonary pseudolymphoma']",,178610,60026,C1867419,,,,,,,,
mondo:0008349,"pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities","['pulmonic stenosis, atrial septal defect, and unique electrocardiographic abnormalities', 'Ciuffo syndrome']",,178650,,C1867407,,,,C566733,,,,
mondo:0008350,pulmonic stenosis and deafness,['pulmonic stenosis and deafness'],,178651,,C1867406,,,,,,,,
mondo:0008352,"pupillary membrane, persistence of","['pupillary membrane, persistence of']",,178900,,,,,,C562700,,,,
mondo:0008353,pruritic urticarial papules and plaques of pregnancy,"['polymorphic eruption of pregnancy', 'pruritic urticarial papules and plaques of pregnancy', 'PUPPP', 'pruritic urticarial papules and plaques of pregnancy, familial (subtype)', 'pruritic urticarial papules plaques of pregnancy']",,178995,64745,,,,,C535817,692.9,,10066100,
mondo:0008354,purpura simplex,['purpura simplex'],,179000,,C0272309,,,,C536249,287.2,,,
mondo:0008355,"pyloric stenosis, infantile hypertrophic, 1","['pyloric stenosis, infantile hypertrophic', 'pyloric stenosis, infantile hypertrophic 1, multifactorial', 'pyloric stenosis, infantile hypertrophic, 1', 'IHPS1', 'pyloric stenosis, infantile']",,179010,,C1867403,,,,,,,,
mondo:0008356,"radial heads, posterior dislocation of","['radial heads, posterior dislocation of']",,179200,,C1867398,,,,C566728,,,,
mondo:0008357,radial hypoplasia-triphalangeal thumbs-hypospadias-maxillary diastema syndrome,"['Schmitt-Gillenwater-Kelly syndrome', 'Schmitt Gillenwater Kelly syndrome', 'radial hypoplasia, triphalangeal thumbs and hypospadias', 'radial hypoplasia, triphalangeal thumbs, hypospadias, and maxillary diastema', 'radial hypoplasia triphalangeal thumbs hypospadias maxillary diastema']",,179250,2252,,,,,C536262,,,,
mondo:0008358,radial ray hypoplasia-choanal atresia syndrome,"['radial ray hypoplasia and choanal atresia', 'radial RAY hypoplasia with choanal atresia', 'Goldblatt-Viljoen syndrome', 'radial ray hypoplasia choanal atresia']",,179270,3026,,,,,,,,,
mondo:0008359,radio-renal syndrome,"['radial-renal syndrome', 'radio renal syndrome']",,179280,3015,C2931146,,,,C536267,,,,
mondo:0008361,"radius, aplasia of, with cleft lip/palate","['radius, aplasia of, with cleft lip/palate']",,179400,,C1867395,,,,,,,,
mondo:0008362,ragweed sensitivity,['ragweed sensitivity'],,179450,,,,,,C566725,,,,
mondo:0008363,raindrop hypopigmentation,['raindrop hypopigmentation'],,179500,,,,,,C566724,,,,
mondo:0008364,Raynaud disease,"['Raynaud^s disease', 'Raynaud syndrome', 'secondary Raynaud^s phenomenon', 'Raynaud^s syndrome', 'Raynaud^s syndrome (disorder) [ambiguous]', 'Raynaud disease', 'secondary Raynaud phenomenon', 'secondary Raynaud disease', 'cold fingers, hereditary', 'secondary Raynaud^s disease']",10300,179600,,C0034734,,C116359,1001145,D011928,443.0,I73.0,,
mondo:0008365,recombinant 8 syndrome,"['San Luis Valley syndrome', 'Rec8 syndrome', 'RECOMBINANT chromosome 8 syndrome', 'San Luis Valley recombinant chromosome 8 syndrome', 'Recombinant chromosome 8 syndrome', 'Rec(8) syndrome', 'Duplication 8q/deletion 8p', 'chromosome 8Q22.1-qter Duplication and 8Pter-p23.1 deletion']",,179613,96167,C0795822,,,,C535296,,,,
mondo:0008366,red cell permeability defect,"['elliptocytosis with transverse slitlike changes', 'red cell permeability defect']",,179650,,C1867340,,,,,,,,
mondo:0008367,red cell phospholipid defect with hemolysis,"['leaky Red cell syndrome', 'high Red cell phosphatidylcholine hemolytic Anemia', 'phosphatidylcholine Red cell Membrane disorder', 'HPCHA', 'high Red cell phosphatidylcholine hemolytic Anaemia', 'red cell phospholipid defect with hemolysis']",,179700,,C1867339,,,,C535298,,,,
mondo:0009440,"ichthyosiform erythroderma, corneal involvement, and hearing loss","['KID syndrome, autosomal recessive', 'ichthyosiform erythroderma, corneal involvement, deafness', 'Desmons syndrome', 'ichthyosiform erythroderma, corneal involvement, and deafness', 'keratitis-ichthyosis-deafness syndrome, autosomal recessive']",,242150,,C1275089,,,,C537363,,,,
mondo:0009441,autosomal recessive congenital ichthyosis 1,"['LI1', 'ichthyosis congenita 2', 'ARCI1', 'lamellar exfoliation of newborn', 'collodion fetus', 'ichthyosis, lamellar, 1', 'ichthyosis, congenital, autosomal recessive 1, with bathing suit distribution', 'autosomal recessive congenital ichthyosis type 1', 'lamellar ichthyosis, type 1', 'collodion baby, self-healing', 'ichthyosis, congenital, autosomal recessive 1', 'ichthyosis, lamellar, 1, formerly', 'ichthyosis congenita', 'ichthyosis, congenital, autosomal recessive type 1', 'bathing suit ichthyosis', 'desquamation of newborn', 'collodion foetus', 'ichthyosis lamellar 1']",0060656,242300,313,C3536797,"['-0.2172', '0.4617', '-0.3464', '-0.1506', '-0.1015', '-1.192', '-0.6973', '0.7515', '-0.3816', '-0.916', '0.015236', '0.1283', '-0.01251', '0.2064', '-0.302', '0.165', '0.1874', '-0.36', '-0.1682', '-0.7817', '-0.7476', '-0.0493', '0.65', '-0.2462', '0.0648', '0.608', '-0.4766', '0.586', '0.2009', '-0.07465', '0.1473', '-0.1454', '-0.1833', '0.3203', '-0.322', '0.6846', '0.1631', '-0.2534', '0.1594', '0.0579', '0.2178', '-0.669', '-0.1129', '0.1487', '-0.09076', '-0.207', '-0.1054', '-0.2085', '0.603', '-0.1367', '-0.0872', '-1.14', '0.1934', '0.0186', '-0.37', '-0.003096', '0.1779', '0.274', '-0.06168', '-0.4458', '0.12396', '-0.08966', '-0.365', '0.2394', '0.597', '-0.129', '0.6494', '0.04877', '-0.1724', '0.813', '0.2332', '-0.0705', '0.0417', '-0.1831', '-0.1313', '0.503', '-0.188', '0.07117', '-0.231', '-0.06107', '-0.3943', '0.2135', '-0.1132', '-0.2883', '-0.04922', '0.05148', '0.007393', '0.558', '0.1175', '0.2399', '0.2913', '0.4695', '0.7383', '0.27', '0.1562', '0.1858', '0.3057', '-0.4172', '0.2986', '-0.59']",,,D017490,,,,
mondo:0009442,ichthyosis congenita with biliary atresia,"['ichthyosis congenita with biliary atresia', 'ichthyosis congenita biliary atresia', 'congenital ichthyosis with biliary atresia']",,242400,,,,,,C562886,,,,
mondo:0009443,autosomal recessive congenital ichthyosis 4B,"['ichthyosis fetalis, Harlequin type', 'ichthyosis, congenital, autosomal recessive type 4B', 'ichthyosis congenita, Harlequin type', 'autosomal recessive congenital ichthyosis type 4B', 'hi', 'ichthyosis congenita, Harlequin fetus type', 'ichthyosis congenita, Harlequin foetus type', 'ichthyosis , congenital, autosomal recessive 4b (harlequin)', 'ichthyosis, congenital, autosomal recessive 4B', '^Harlequin fetus^', 'harlequin type ichthyosis fetalis', 'ARCI4B', 'harlequin ichthyosis', 'Harlequin foetus', 'Harlequin fetus', 'harlequin type ichthyosis congenita']",0060713,242500,457,C0239849,"['0.2384', '-0.2452', '0.10736', '0.0813', '0.1328', '-0.833', '-0.5503', '0.509', '-0.1466', '-0.6064', '0.2488', '-0.03873', '0.296', '0.1218', '-0.6743', '0.11285', '0.1302', '-0.2239', '-0.2374', '-1.378', '-0.381', '0.02574', '0.621', '0.1489', '-0.2461', '0.602', '-0.536', '0.2505', '0.3967', '-0.7124', '0.8457', '0.2673', '-0.4343', '0.355', '-0.0884', '0.3215', '-0.1848', '-0.09406', '-0.2712', '-0.311', '-0.2686', '0.01424', '-0.0948', '0.3604', '-0.2751', '-0.2294', '-0.8125', '-0.543', '0.6304', '0.1744', '-0.6675', '-1.21', '0.3796', '-0.4712', '-0.4812', '-0.4197', '0.1246', '0.1935', '-0.3357', '-0.141', '0.2886', '0.532', '-0.2206', '0.4106', '-0.01979', '-0.09015', '0.6323', '-0.00805', '-0.185', '0.8574', '-0.3188', '0.02612', '0.0854', '0.2905', '-0.08307', '0.376', '-0.03238', '-0.462', '-0.1646', '-0.4404', '-0.1575', '-0.0255', '-0.3845', '0.4604', '0.0779', '0.5654', '-0.4104', '0.2715', '-0.02626', '0.29', '0.03021', '0.5415', '0.507', '0.6123', '-0.2974', '0.2607', '0.4084', '-0.3623', '0.2524', '0.367']",C98934,,,,,10019163,
mondo:0009444,ichthyosis-alopecia-eclabion-ectropion-intellectual disability syndrome,"['Jagell-Holmgren-Hofer syndrome', 'ichthyosis alopecia eclabion ectropion mental retardation', 'ichthyosis with alopecia, eclabium, ectropion, and intellectual disability', 'ichthyosis with alopecia, eclabium, ectropion, and mental retardation', 'ichthyosis alopecia eclabion ectropion intellectual disability', 'Jagell Holmgren Hofer syndrome']",,242510,2269,C1855788,,,,C537364,,,,
mondo:0009445,ichthyosis-hepatosplenomegaly-cerebellar degeneration syndrome,"['Dykes Markes Harper syndrome', 'Dykes-Markes-Harper syndrome', 'Dykes-Marks-Harper syndrome', 'ichthyosis, hepatosplenomegaly, and cerebellar degeneration']",,242520,2274,C1275088,,,,C535727,571.8,,,
mondo:0009446,ichthyosis-intellectual disability-dwarfism-renal impairment syndrome,"['ichthyosis, mental retardation, dwarfism and renal impairment', 'Passwell-Goodman-Siprkowski syndrome', 'ichthyosis, mental retardation, dwarfism, and renal impairment', 'ichthyosis, intellectual disability, dwarfism and renal impairment', 'ichthyosis, intellectual disability, dwarfism, and renal impairment', 'ichthyosis intellectual deficit dwarfism renal impairment']",,242530,2278,C1855787,,,,C536274,,,,
mondo:0009447,"ichthyosis, split hairs, and amino aciduria","['ichthyosis, split hairs, and amino aciduria']",,242550,,C1855786,,,,C565471,,,,
mondo:0009448,iminoglycinuria,"['iminoglycinuria, digenic', 'iminoglycinuria']",0112265,242600,42062,C0268654,"['-0.2585', '0.3875', '-0.091', '-0.2524', '0.3474', '-0.4084', '-0.4106', '0.2654', '-0.10205', '0.04166', '-0.1774', '-0.04105', '0.0771', '0.05966', '0.04672', '0.0603', '0.03897', '-0.0648', '-0.03647', '-0.512', '-0.2299', '-0.4038', '0.63', '-0.05893', '-0.0767', '-0.1372', '0.2832', '-0.1449', '0.04602', '0.02466', '0.2101', '-0.006336', '0.0675', '0.1708', '-0.524', '-0.1627', '0.0843', '-0.1294', '0.0584', '-0.3174', '-0.00738', '-0.4722', '0.4385', '-0.466', '-0.5146', '-0.596', '0.1566', '-0.1836', '0.1831', '0.1777', '0.1058', '-0.1766', '-0.1353', '-0.4556', '-0.1108', '-0.2617', '0.6216', '-0.0091', '-0.4404', '0.1377', '0.327', '0.004803', '0.2776', '0.02483', '0.2225', '0.075', '0.3481', '0.02972', '-0.5303', '-0.06775', '-0.2566', '-0.232', '-0.1836', '0.05185', '0.3', '0.375', '0.09235', '0.0549', '-0.07556', '-0.1583', '0.1564', '0.2554', '-0.006107', '0.0664', '0.03378', '0.2961', '0.05087', '-0.2595', '0.11395', '0.1406', '0.09894', '0.2448', '-0.4465', '-0.1919', '0.4604', '0.256', '0.324', '-0.534', '-0.4097', '0.03583']",,,C536285,270.8,,,
mondo:0009449,ciliary dyskinesia with defective radial spokes,"['ciliary dyskinesia with defective radial spokes', 'immotile cilia syndrome, due to defective radial spokes', 'cilia with defective radial spokes', 'immotile cilia syndrome due to defective radial spokes']",,242670,,C0340035,,,,C536286,759.89,,,
mondo:0009450,ciliary dyskinesia with excessively long cilia,"['ciliary dyskinesia with excessively long cilia', 'immotile cilia syndrome due to excessively long cilia']",,242680,,,,,,C536287,759.89,,,
mondo:0009451,Nezelof syndrome,"['immune defect due to absence of THYMUS', 'immune defect due to absence Of Thymus', 'Nezelof^s syndrome', 'thymic aplasia', 'Nezelof syndrome', 'T-lymphocyte deficiency']",2012,242700,83471,CN206066,"['-0.1112', '0.1603', '-0.2172', '-0.4402', '0.2585', '0.0339', '0.01286', '0.1185', '-0.2377', '-0.2128', '-0.1198', '-0.0695', '-0.3137', '-0.03983', '-0.1616', '0.02898', '0.2233', '0.1306', '-0.4028', '-0.526', '-0.1196', '-0.2006', '0.495', '-0.1686', '0.178', '0.061', '-0.0632', '0.06464', '-0.0482', '-0.4724', '0.3591', '0.1569', '0.3232', '0.1886', '0.02867', '0.0876', '-0.4104', '0.1631', '-0.1895', '-0.2446', '-0.1643', '-0.1152', '0.1167', '-0.1042', '-0.2458', '-0.4539', '-0.00415', '-0.1667', '0.0001046', '0.2161', '-0.06616', '-0.04483', '0.3445', '-0.131', '-0.3064', '-0.00457', '0.2382', '-0.45', '-0.2133', '0.0991', '0.1975', '0.1417', '-0.04144', '0.03647', '0.2925', '-0.2349', '0.3418', '0.3203', '-0.1377', '0.2056', '-0.3562', '-0.05087', '-0.0434', '-0.08264', '-0.07007', '-0.2515', '0.3145', '0.0417', '0.1302', '0.08636', '-0.1525', '-0.06433', '0.1614', '0.0826', '-0.2568', '-0.06683', '0.1525', '0.04645', '0.0823', '-0.05408', '0.1818', '0.1855', '-0.11523', '0.0843', '0.639', '0.4426', '0.1565', '-0.2443', '0.02719', '0.289']",,,C536288,279.13,,,
mondo:0009452,Vici syndrome,"['immunodeficiency with cleft lip/palate, cataract, hypopigmentation, and absent corpus callosum', 'Dionisi Vici Sabetta Gambarara syndrome', 'immunodeficiency with cleft lip/palate, cataract, hypopigmentation and absent corpus callosum', 'Dionisi-Vici-Sabetta-Gambarara syndrome', 'VICIS', 'immunodeficiency with cleft Lip/palate, cataract, hypopigmentation, and absent corpus callosum', 'absent corpus callosum-cataract-immunodeficiency syndrome', 'absent corpus callosum cataract immunodeficiency', 'corpus callosum agenesis-cataract-immunodeficiency syndrome', 'Vici syndrome']",0060356,242840,1493,C1855772,"['0.4504', '0.2365', '-0.1907', '-0.351', '0.3928', '0.1484', '0.1743', '0.5176', '-0.1768', '-0.641', '0.1288', '-0.5337', '-0.4978', '0.2556', '-0.3513', '0.05066', '-0.2069', '-0.745', '-0.1458', '-0.7036', '0.3367', '-0.08673', '0.3447', '-0.0562', '0.04257', '-0.1897', '-0.654', '0.1913', '0.3992', '-0.3643', '0.6978', '-0.01474', '0.385', '-0.2258', '-0.2708', '0.2527', '-0.09015', '-0.8467', '-0.08795', '0.283', '-0.2651', '0.2242', '0.4067', '0.3645', '-0.311', '-0.278', '-0.09595', '-0.4534', '0.0983', '0.3896', '-0.619', '0.68', '0.2284', '0.02916', '-0.3516', '-0.00524', '0.7686', '-0.289', '-0.1686', '0.1317', '0.0631', '0.1327', '-0.1193', '0.1533', '0.1459', '-0.2341', '0.2479', '0.5107', '-0.6167', '0.221', '-0.1693', '-0.1843', '-0.5034', '0.1359', '0.01501', '-0.476', '0.8306', '-0.6514', '0.1923', '0.277', '0.2751', '0.1699', '-0.1295', '0.5093', '-0.3228', '0.3635', '0.1694', '0.2423', '0.4592', '0.2976', '0.1229', '0.1283', '-0.339', '-0.009026', '0.53', '0.2108', '0.1098', '0.0727', '0.2769', '0.698']",C138174,,C535566,,,,
mondo:0009453,immune deficiency disease,['immune deficiency disease'],,242850,,C1855771,,,,C565469,,,,
mondo:0009454,immunodeficiency-centromeric instability-facial anomalies syndrome 1,"['ICF1', 'centromeric instability, immunodeficiency syndrome', 'DNMT3B immunodeficiency-centromeric instability-facial anomalies syndrome', 'immunodeficiency-centromeric instability-facial anomalies syndrome type 1', 'immunodeficiency syndrome, variable', 'ICF syndrome 1', 'immunodeficiency-centromeric instability-Facial anomalies syndrome type 1', 'immunodeficiency-centromeric instability-facial anomalies syndrome caused by mutation in DNMT3B', 'immunodeficiency-centromeric instability-facial anomalies syndrome 1', 'immune deficiency, variable, with centromeric instability of chromosomes 1, 9, and 16']",0090008,242860,,,,C156430,,,,,,
mondo:0009455,"immunodeficiency, partial combined, with absence of HLA Determinants and beta-2-microglobulin from lymphocytes","['immunodeficiency, partial combined, with absence of HLA Determinants and beta-2-microglobulin from lymphocytes']",,242870,,C1855762,,,,C565468,,,,
mondo:0009456,Immunoerythromyeloid hypoplasia,['Immunoerythromyeloid hypoplasia'],,242880,,CN074232,,,,,,,,
mondo:0009457,"immunoglobulin d level in plasma, low","['IMMUNOGLOBULIN D level in plasma, LOW']",,242890,,,,,,,,,,
mondo:0009458,Schimke immuno-osseous dysplasia,"['Schimke syndrome', 'IMMUNOOSSEOUS dysplasia, Schimke type', 'Schimke IMMUNOOSSEOUS dysplasia', 'Schimke Immunoosseous dysplasia', 'SIOD', 'spondyloepiphyseal dysplasia-nephrotic syndrome', 'Schimke immunoosseous dysplasia', 'immunoosseous dysplasia Schimke type', 'spondyloepiphyseal dysplasia nephrotic syndrome', 'spondyloepiphyseal dysplasia - nephrotic syndrome']",0060490,242900,1830,C0877024,"['-0.2607', '0.11835', '0.2612', '-0.5586', '0.1216', '0.0564', '0.4097', '0.3826', '-0.6333', '-0.512', '0.1362', '-0.1033', '0.7427', '0.3582', '-0.4385', '0.165', '0.6294', '0.4443', '-0.1432', '-0.7188', '0.42', '0.03757', '0.7607', '0.2869', '-0.07947', '-0.272', '-0.01425', '-0.1326', '0.2742', '-0.6416', '0.4167', '0.5244', '0.73', '-0.186', '0.3074', '-0.2383', '-0.3276', '-0.05734', '-0.1477', '-0.2651', '-0.2272', '0.2598', '0.6', '0.01209', '0.199', '-0.607', '-0.1072', '-0.01978', '0.4695', '-0.3218', '-0.4958', '0.455', '0.3955', '0.1105', '-0.433', '-0.4133', '0.00979', '-0.8423', '-0.5015', '0.3083', '0.011894', '-0.0851', '-0.1863', '0.4385', '0.6816', '-0.221', '0.22', '0.02635', '0.2003', '0.553', '-0.4795', '-0.6665', '-0.4487', '0.12463', '-0.3264', '0.544', '0.2482', '0.1373', '0.366', '0.3474', '0.0159', '0.01643', '-0.3003', '0.069', '-0.642', '0.135', '0.501', '-0.1753', '0.06604', '0.3943', '0.01985', '-0.02032', '-0.1342', '-0.368', '1.0', '0.4287', '0.1396', '-0.1484', '0.6', '0.4812']",C135087,,C536629,,,10048699,
mondo:0009459,"channelopathy-associated congenital insensitivity to pain, autosomal recessive","['channelopathy-associated CIP', 'indifference to pain, congenital, autosomal recessive', 'HSAN2D', 'congenital analgesia, autosomal recessive', 'neuropathy, hereditary sensory and autonomic, type 2D', 'asymbolia for pain', 'insensitivity to pain, congenital', 'insensitivity to pain, channelopathy-associated', 'neuropathy, hereditary sensory and autonomic, type IID', 'HSAN2D, AR', 'CIP']",,243000,88642,C1855739,"['-0.302', '0.2588', '0.0692', '-0.09436', '0.2283', '-0.1274', '-0.3574', '-0.01087', '-0.01366', '-0.2146', '0.1812', '0.141', '-0.11176', '-0.1699', '0.1775', '0.4058', '0.1241', '-0.1927', '-0.01035', '-0.3289', '-0.1332', '0.1066', '-0.09015', '-0.05283', '0.1328', '0.212', '0.00978', '0.0663', '-0.1719', '-0.2546', '0.06415', '-0.1279', '0.471', '0.264', '-0.1403', '-0.4631', '-0.02762', '-0.1305', '0.2028', '-0.506', '0.004185', '-0.2194', '-0.0674', '-0.2448', '0.02687', '-0.3538', '-0.1344', '0.24', '0.203', '0.3728', '0.2294', '0.1164', '0.03403', '0.0988', '0.2754', '0.05814', '0.3264', '-0.0792', '-0.2366', '-0.03278', '0.02527', '0.0706', '0.2365', '0.02673', '0.0345', '0.1311', '0.4795', '0.2047', '-0.4304', '0.0925', '-0.397', '0.05646', '0.1019', '-0.1619', '0.3484', '0.4827', '0.1377', '0.3337', '0.0885', '-0.01587', '0.2449', '0.2742', '0.3013', '0.527', '0.00349', '0.1462', '-0.1283', '0.2184', '0.079', '0.3538', '0.2295', '0.254', '-0.1711', '0.12384', '0.3335', '0.12335', '0.395', '-0.287', '0.01797', '0.2498']",,,,,,,
mondo:0009460,indolylacroyl glycinuria with intellectual disability,"['indolylacroyl glycinuria with intellectual disability', 'indolylacroyl glycinuria with mental retardation']",,243050,,C1855738,,,,C565466,,,,
mondo:0009461,spermatogenic failure 5,"['spermatogenic failure type 5', 'male infertility due to large-headed multiflagellar polyploid spermatozoa', 'male infertility with large-headed, multiflagellar, polyploid spermatozoa', 'infertility associated with multi-tailed spermatozoa and excessive DNA', 'infertility associated with multitailed spermatozoa and excessive DNA', 'spermatogenic failure 5', 'male infertility due to macrozoospermia', 'macrocephalic sperm head syndrome', 'macrozoospermia', 'SPGF5']",0070183,243060,137893,C0403812,"['-0.38', '-0.687', '0.1707', '-0.586', '-0.097', '-0.4485', '0.02669', '0.619', '-0.4744', '-0.3938', '1.66', '-0.0711', '-0.1494', '1.27', '-0.04166', '-0.1685', '0.1637', '0.6963', '-0.653', '-1.3', '-0.2725', '0.0682', '0.393', '-0.494', '0.3945', '-0.782', '0.349', '0.08453', '-0.713', '-0.4211', '0.566', '-0.1732', '-0.2732', '-0.193', '0.0326', '0.0885', '-0.3125', '0.10706', '0.1776', '-0.1261', '0.2014', '0.3232', '0.2546', '-0.392', '0.759', '-0.7954', '0.4136', '-0.9497', '0.677', '0.3516', '-0.728', '-0.1223', '-0.0863', '0.66', '0.02608', '0.611', '0.1306', '0.1738', '-0.7524', '0.1997', '0.2435', '0.9478', '-0.1437', '0.1323', '-0.332', '0.503', '0.02306', '0.598', '-1.121', '0.6704', '-0.4348', '0.2546', '-0.1082', '-0.1681', '0.1526', '0.7563', '0.3853', '0.4998', '-0.2427', '0.2327', '-0.06824', '0.424', '0.02573', '-0.7617', '-0.1148', '-0.706', '0.1409', '0.05045', '0.4785', '-0.588', '-0.6235', '0.3242', '-0.6196', '1.117', '0.494', '-0.2688', '0.09656', '-0.458', '-0.718', '0.0855']",,,C562903,,,,
mondo:0009462,"inosine phosphorylase deficiency, immune defect due to","['inosine phosphorylase deficiency, immune defect due to']",,243080,,C1855737,,,,C565465,,,,
mondo:0009463,"internal carotid arteries, hypoplasia of","['internal carotid arteries, hypoplasia of']",,243100,,,,,,,,,,
mondo:0009464,immunodeficiency with defective T-cell response to interleukin 1,"['immunodeficiency with defective T-cell response to interleukin 1', 'immunodeficiency with defective T-cell response to Interleukin type 1', 'Interleukin 1, defective T-cell response to']",,243110,,C1855735,,,,,,,,
mondo:0009465,multiple intestinal atresia,"['combined immunodeficiency-enteropathy spectrum', 'intestinal atresia multiple', 'intestinal atresia, multiple and/or inflammatory bowel disease with or without immunodeficiency', 'GIDID', 'multiple gastrointestinal atresias', 'intestinal atresia, multiple', 'familial intestinal polyatresia syndrome', 'gastrointestinal defects and immunodeficiency syndrome', 'CID-MIA/early-onset IBD']",14671,,436252,,"['-0.615', '0.2148', '0.3015', '-0.1616', '0.0579', '-0.2103', '-0.075', '-0.1559', '0.0531', '0.2568', '-0.0661', '-0.1272', '-0.342', '-0.1421', '-0.4663', '-0.3162', '0.1138', '0.2952', '-0.1737', '-0.628', '0.08276', '-0.3396', '0.6167', '-0.2164', '0.365', '-0.02896', '0.0647', '0.4202', '0.05', '-0.2642', '0.488', '0.02182', '0.1855', '0.02629', '0.2583', '0.0173', '-0.912', '0.3247', '-0.2927', '0.1011', '-0.2399', '-0.2542', '0.3743', '-0.43', '-0.2722', '-0.213', '-0.1101', '0.0285', '-0.2151', '0.2395', '-0.4133', '-0.127', '0.4368', '-0.2416', '-0.503', '-0.2235', '-0.2413', '-0.1621', '-0.2861', '0.03528', '0.3037', '0.337', '0.00958', '-0.09686', '0.3794', '0.003855', '0.439', '0.2421', '-0.3186', '0.3108', '-0.1', '0.1123', '0.1621', '0.08246', '-0.0873', '-0.1293', '0.2147', '0.01915', '0.349', '0.02554', '-0.42', '-0.07965', '-0.04126', '-0.2351', '-0.2634', '-0.1394', '0.0732', '0.0863', '0.299', '-0.6025', '0.2134', '0.4478', '0.01566', '0.0678', '0.5347', '0.5386', '0.0822', '-0.5293', '0.00967', '0.3489']",,,C562441,751.8,,10028210,
mondo:0009467,natal teeth-intestinal pseudoobstruction-patent ductus syndrome,"['Natal teeth, intestinal pseudoobstruction and patent ductus', 'intestinal pseudoobstruction with patent ductus arteriosus and NATAL teeth']",,243185,1654,C1855732,,,,C538341,,,,
mondo:0009468,pseudotumor cerebri,"['benign intracranial hypertension', 'intracranial hypertension, idiopathic', 'pseudotumor cerebri', 'idiopathic intracranial hypertension', 'IIH', 'benign intracran. hypt.']",11459,243200,238624,C0033845,,C85035,1001132,D011559,348.2,,10037149,
mondo:0009469,benign recurrent intrahepatic cholestasis type 1,"['benign recurrent intrahepatic cholestasis caused by mutation in ATP8B1', 'cholestasis, benign recurrent intrahepatic 1', 'cholestasis, benign recurrent intrahepatic, 1', 'BRIC1', 'mild ATP8B1 deficiency', 'Bric type 1', 'benign recurrent intrahepatic cholestasis 1', 'cholestasis, benign recurrent intrahepatic, type 1', 'cholestasis, benign recurrent intrahepatic', 'ATP8B1 benign recurrent intrahepatic cholestasis', 'Summerskill syndrome', 'recurrent familial intrahepatic cholestasis 1']",0070231,243300,99960,,"['-0.03096', '0.237', '-0.342', '0.2546', '-0.01718', '-0.2595', '0.2283', '-0.26', '-0.1547', '0.1338', '-0.2788', '-0.2379', '-0.3196', '0.4045', '-0.1968', '-0.4233', '0.0995', '-0.1104', '0.295', '-0.568', '-0.351', '-0.1544', '0.531', '-0.1936', '0.157', '-0.3196', '0.1548', '0.352', '-0.01347', '0.0767', '0.601', '0.02255', '-0.2268', '-0.04846', '-0.1031', '-0.1059', '-0.3945', '0.09485', '-0.01162', '0.358', '-0.005234', '-0.5234', '-0.03552', '0.3157', '-0.3267', '0.2258', '-0.1661', '-0.0574', '0.4722', '0.2029', '-0.0922', '0.00877', '-0.1718', '-0.0373', '-0.010086', '0.1486', '-0.2554', '0.2023', '-0.339', '0.508', '0.2402', '0.01279', '0.5137', '-0.2861', '0.1805', '-0.06186', '0.6196', '0.2988', '-0.4036', '0.3982', '0.1509', '0.2155', '0.5537', '-0.2659', '0.3467', '0.3281', '0.4648', '0.533', '-0.02391', '0.2188', '-0.2136', '-0.526', '-0.413', '-0.3674', '-0.04004', '-0.2185', '0.2056', '-0.04205', '0.4236', '0.03503', '0.3481', '0.3865', '-0.1315', '0.06433', '0.724', '0.2861', '-0.03854', '-0.5127', '-0.1554', '0.411']",,,,,,,
mondo:0009470,Baraitser-Winter syndrome 1,"['cerebrofrontofacial syndrome', 'cerebrooculofacial lymphatic syndrome', 'intellectual disability with epilepsy and characteristic facies', 'mental retardation with epilepsy and characteristic facies', 'BRWS1', 'Fryns-Aftimos syndrome', 'Baraitser-Winter syndrome type 1', 'Baraitser-WINTER syndrome 1', 'iris coloboma with ptosis, hypertelorism, and intellectual disability', 'pachygyria, intellectual disability, epilepsy, and characteristic facies', 'chromosome 7P22 deletion syndrome', 'Baraitser-Winter syndrome 1', 'ACTB Baraitser-Winter cerebrofrontofacial syndrome', 'Baraitser-Winter cerebrofrontofacial syndrome caused by mutation in ACTB', 'iris coloboma with ptosis, hypertelorism, and mental retardation', 'ACTB-related BAFopathy', 'pachygyria, mental retardation, epilepsy, and characteristic facies']",0081112,243310,,C1853623,,,,,,,,
mondo:0009471,"intrinsic factor and r binder, combined congenital deficiency of","['intrinsic factor and r binder, combined congenital deficiency of']",,243320,,C1855721,,,,C565461,,,,
mondo:0009472,"acetylation, slow","['acetylation, Fast', 'Isoniazid inactivation, slow', 'Fast acetylator phenotype', 'acetylation, slow', 'INH inactivation, Fast', 'slow acetylator phenotype', 'INH inactivation, slow']",,243400,,,,,,,,,,
mondo:0009473,isotretinoin-like syndrome,"['Kawashima syndrome', 'microtia-aortic arch syndrome', 'syndrome of microtia and aortic arch anomalies', 'microtia aortic arch syndrome', 'Isotretinoin embryopathy like syndrome', 'ISOTRETINOIN embryopathy-like syndrome', 'microtia-aortic Arch syndrome']",,243440,2306,,,,,C535542,,,,
mondo:0009474,"isovaleric acid, inability to smell","['isovaleric acid, inability to smell']",,243450,,,,,,,,,,
mondo:0009475,isovaleric acidemia,"['isovaleric acid CoA dehydrogenase deficiency', 'isovaleryl-CoA dehydrogenase deficiency', 'Isovalericacidemia', 'IVA', 'IVD deficiency', 'isovaleric aciduria', 'isovaleric acid Coa dehydrogenase deficiency', 'isovaleryl CoA carboxylase deficiency', 'isovaleric acidemia']",14753,243500,33,C0268575,"['0.1826', '0.3525', '-0.5073', '0.2751', '0.2708', '-0.571', '-0.1113', '0.1449', '0.1566', '-0.0828', '-0.0743', '-0.2605', '0.7056', '0.11774', '-0.374', '0.2761', '0.184', '-0.521', '-0.3838', '-0.9204', '-0.2347', '-0.556', '0.8555', '-0.299', '0.4458', '-0.4724', '-0.09863', '0.08075', '0.3599', '-0.6655', '0.4727', '-0.3235', '0.4863', '0.4207', '-0.8457', '0.3127', '-0.1729', '0.439', '-0.1511', '-0.0705', '-0.0625', '-0.6084', '0.601', '-0.079', '-0.1321', '-0.5024', '-0.09595', '-0.574', '0.0643', '0.5293', '-0.505', '-0.1566', '-0.4194', '-0.4468', '0.61', '-0.414', '0.2434', '-0.399', '-0.10736', '0.8496', '0.4897', '0.1113', '0.2378', '-0.2094', '-0.1582', '0.771', '0.2524', '0.598', '0.3276', '0.5176', '-0.395', '0.2803', '-0.3345', '0.2422', '0.2727', '0.02711', '0.5547', '-0.0746', '0.1142', '-0.07184', '0.4216', '-0.358', '-0.2002', '0.1015', '0.6523', '0.8774', '-0.01024', '-0.1285', '0.3374', '0.3992', '0.511', '0.3398', '-0.925', '0.3237', '-0.07086', '1.168', '0.0745', '-0.491', '-0.4773', '-0.1242']",C98964,,C538167,,E71.110,,
mondo:0009476,atresia of small intestine,"['small intestine atresia', 'apple peel syndrome', 'APSB', 'congenital atresia of the small intestine', 'congenital small intestine atresia', 'intestinal atresia type IIIb', 'jejunal atresia', 'familial apple peel jejunal atresia', 'small intestinal atresia', 'apple peel small bowel syndrome', 'atresia of the small intestine', 'Jejunoileal atresia', 'apple-peel intestinal atresia']",,243600,1201,C0266172,,C98828,,C538260,,,10010626,
mondo:0009477,Stromme syndrome,"['apple peel syndrome with microcephaly and ocular anomalies', 'ciliary dyskinesia, primary, 31, formerly', 'lethal fetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome', 'jejunal atresia with microcephaly and ocular anomalies', 'primary ciliary dyskinesia 31', 'STROMS', 'CILD31', 'apple-peel intestinal atresia-ocular anomalies-microcephaly syndrome', 'lethal foetal brain malformation-duodenal atresia-bilateral renal hypoplasia syndrome', 'jejunal atresia-microcephaly-ocular anomalies syndrome', 'Stromme syndrome', 'ciliary dyskinesia, primary, 31', 'ciliary dyskinesia, primary, type 31']",0110595,616369,506307,CN237682,"['-0.05698', '0.0807', '-0.07733', '-0.4385', '-0.12354', '-0.2783', '-0.02975', '0.2568', '-0.5244', '-0.4114', '0.03717', '-0.3796', '-0.04276', '-0.171', '-0.2029', '-0.1509', '-0.04407', '-0.2461', '-0.1249', '-0.4285', '0.1615', '-0.01575', '0.2798', '-0.4185', '0.3535', '-0.03278', '-0.4382', '0.02083', '0.328', '-0.3447', '0.2285', '-0.2155', '0.3247', '0.2299', '0.371', '0.00567', '-0.4001', '-0.322', '-0.2893', '-0.0356', '0.0384', '-0.0375', '0.005196', '-0.1904', '-0.0516', '-0.4534', '0.3037', '0.08405', '-0.4905', '-0.04517', '-0.0561', '0.164', '-0.3118', '-0.2018', '-0.47', '-0.336', '-0.05093', '-0.10583', '-0.09686', '0.2815', '0.325', '0.0254', '-0.3281', '0.1272', '-0.1549', '-0.09784', '0.2073', '0.2156', '-0.1849', '0.415', '-0.552', '0.1445', '-0.0595', '0.0523', '-0.1825', '-0.0737', '0.1185', '-0.1936', '-0.1503', '-0.03296', '-0.0506', '0.1287', '0.11426', '0.672', '-0.131', '0.01236', '-0.0499', '0.11835', '-0.0499', '-0.0863', '0.2169', '0.3984', '0.3567', '-0.04733', '0.625', '0.2927', '0.605', '-0.2346', '0.3643', '0.585']",,0009160,C565460,,,,
mondo:0009478,combined immunodeficiency due to DOCK8 deficiency,"['DOCK8 immunodeficiency syndrome', 'HIES autosomal recessive', 'combined immunodeficiency due to dedicator of cytokinesis 8 protein deficiency', 'hyperimmunoglobulin E recurrent infection syndrome, autosomal recessive', 'hyper Ig E syndrome, autosomal recessive', 'hyper-IgE recurrent infection syndrome, autosomal recessive', 'HIES, autosomal recessive', 'dedicator of cytokinesis 8 deficiency', 'DOCK8 deficiency', 'AR-HIES', 'autosomal recessive hyper IgE syndrome', 'AR hyperimmunoglobulin E syndrome', 'Cid due to DOCK8 deficiency', 'hyper-IgE syndrome, autosomal recessive']",0080594,243700,217390,C1968689,"['0.3547', '0.208', '-0.1714', '-0.836', '0.08887', '-0.2944', '0.3325', '-0.155', '0.135', '-0.372', '-0.01682', '0.1902', '-0.6675', '-0.5444', '-0.2817', '0.3906', '0.1309', '-0.1305', '-0.4307', '-0.4414', '-0.3542', '-0.4412', '0.6606', '-0.1896', '0.4539', '0.3552', '-0.428', '0.2505', '-0.25', '-1.019', '0.4', '0.2487', '0.4778', '-0.3152', '0.1852', '-0.3904', '-0.4458', '-0.223', '-0.4065', '-0.1675', '-0.2025', '-0.3887', '0.1785', '0.0632', '-0.1793', '-0.4824', '0.2002', '0.06635', '0.1361', '-0.1976', '-0.2502', '-0.181', '0.2615', '0.1664', '-0.542', '0.2795', '0.2205', '-0.3833', '-0.001461', '0.05606', '0.1624', '0.5894', '-0.353', '0.0117', '0.786', '0.007793', '0.432', '0.4246', '-0.2678', '0.561', '-0.666', '-0.3804', '-0.1853', '0.2725', '-0.02194', '0.0384', '0.1694', '-0.1895', '0.679', '0.6006', '-0.4019', '-0.006294', '0.001622', '0.03903', '0.258', '-0.1565', '0.4058', '0.4014', '0.6426', '-0.1907', '-0.002842', '0.6167', '-0.03403', '0.02858', '0.95', '1.075', '-0.07776', '-0.2866', '-0.3254', '0.09265']",C126343,,,,,,
mondo:0009479,Johanson-Blizzard syndrome,"['Johanson-Blizzard syndrome', 'Johanson-BLIZZARD syndrome', 'JBS', 'nasal alar hypoplasia, hypothyroidism, pancreatic achylia and congenital deafness', 'pancreatic insufficiency, combined exocrine', 'nasal alar hypoplasia, hypothyroidism, pancreatic achylia, and congenital deafness']",14694,260450,2315,C1850081,"['0.11084', '0.3235', '0.6187', '-0.628', '0.724', '-0.05368', '0.3774', '1.019', '-0.0963', '-0.226', '-1.031', '-0.2285', '-0.233', '0.573', '-0.908', '-0.3093', '-0.4397', '-0.3865', '-0.913', '-0.1227', '0.1373', '-0.4382', '0.00464', '-0.2517', '-0.0569', '-0.1843', '-0.2181', '0.1681', '0.882', '-0.946', '0.3047', '0.2744', '0.1907', '0.333', '0.03638', '-0.264', '-0.2039', '-0.552', '-0.3164', '0.3', '-0.2915', '0.2983', '0.454', '-0.1416', '-0.2272', '0.01071', '0.645', '0.827', '-0.0635', '0.2485', '-0.516', '0.05164', '-0.1908', '-0.0976', '-0.4055', '-0.4124', '0.2747', '-0.4292', '-0.366', '0.4028', '0.514', '0.135', '-0.3174', '-0.3232', '-0.2305', '0.6084', '0.1357', '0.4224', '-0.391', '0.0782', '-0.08154', '-0.02382', '-0.1632', '-0.4824', '0.544', '-0.1693', '0.10956', '-0.684', '-0.6577', '-0.06903', '0.01271', '-0.4062', '-0.4106', '-0.1895', '0.03976', '0.05554', '0.2676', '-0.04205', '0.646', '0.2268', '0.10077', '0.6147', '0.4883', '0.074', '0.573', '-1.233', '0.3647', '-0.1675', '0.2573', '0.346']",,0001063,C564907,759.89,,,
mondo:0009480,Joubert syndrome with oculorenal defect,"['Dekaban-Arima syndrome', 'Joubert syndrome with oculorenal defect', 'Joubert syndrome with bilateral chorioretinal coloboma', 'Dekaban Arima syndrome', 'Cerebellooculorenal syndrome', 'CORS', 'coloboma, chorioretinal, with cerebellar vermis aplasia', 'Joubert syndrome with oculorenal anomalies', 'Joubert syndrome 5', 'JS-OR', 'chorioretinal coloboma with cerebellar vermis aplasia', 'JS type B', 'Arima syndrome', 'cerebrooculohepatorenal syndrome', 'cerebello-oculo-renal syndrome', 'Joubert syndrome with Senior-Loken syndrome', 'cerebro-oculo-hepato-renal syndrome']",,243910,2318,C1855675,"['-0.2874', '0.44', '-0.362', '0.1981', '0.0902', '-0.6826', '-0.556', '0.2935', '-0.2551', '-0.5415', '-0.06085', '-0.7383', '-0.0841', '0.1609', '0.1572', '-0.3564', '0.0495', '-0.53', '0.373', '-1.317', '-0.581', '0.02994', '0.4272', '0.01723', '0.3567', '0.418', '-0.663', '0.2566', '0.1503', '0.1869', '0.672', '0.526', '0.396', '0.4353', '0.3223', '0.06238', '-0.2046', '-0.1908', '-0.3374', '0.1742', '-0.00856', '0.05798', '0.5938', '0.1553', '0.2654', '0.424', '-0.4', '0.02919', '0.1213', '0.2788', '0.364', '0.644', '-0.03598', '-0.748', '0.03018', '-0.69', '0.6016', '0.3352', '-0.2273', '0.3677', '0.799', '0.1848', '0.775', '0.5146', '0.1649', '0.0775', '0.954', '0.5054', '-0.8066', '0.562', '-0.4458', '-0.1243', '0.3608', '0.2786', '0.712', '-0.455', '0.33', '0.000205', '-0.4172', '0.2297', '0.3267', '-0.1268', '0.312', '0.2444', '-0.3684', '-0.4255', '0.1837', '0.4373', '0.1375', '-0.2174', '0.06946', '0.2788', '0.249', '0.01933', '0.5864', '0.1658', '0.759', '-0.2454', '0.2861', '0.4265']",,,C537430,,,,
mondo:0009481,Jumping Frenchmen of Maine,"['^jumpers^ of Maine', 'exaggerated startle reflex', 'Jumping Frenchmen of Maine']",,244100,,,,,,,,,,
mondo:0009482,hypogonadotropic hypogonadism 3 with or without anosmia,"['hypogonadotropic hypogonadism caused by mutation in PROKR2', 'PROKR2 hypogonadotropic hypogonadism', 'HH3', 'hypogonadotropic hypogonadism 3 with or without anosmia', 'KAL3', 'Kallmann syndrome 3']",0090092,244200,,C3550478,,,,,,E23.0,,
mondo:0009483,Kapur-Toriello syndrome,"['kapur Toriello syndrome', 'cleft lip/palate-facial, eye, heart and intestinal anomalies syndrome', 'kapur-Toriello syndrome', 'long columella with cleft Lip/palate and eye, heart, and intestinal anomalies', 'long columella with cleft lip/palate and eye, heart and intestinal anomalies']",,244300,2328,C0796005,,,,C537008,,,,
mondo:0009484,primary ciliary dyskinesia 1,"['primary ciliary dyskinesia 1 with or without situs inversus', 'ciliary dyskinesia, primary, type 1', 'CILD1', 'DNAI1 primary ciliary dyskinesia', 'Polynesian bronchiectasis', 'Kartagener syndrome', 'ciliary dyskinesia, primary, 1', 'Siewert syndrome', 'ciliary dyskinesia, primary, 1, with or without situs inversus', 'immotile cilia syndrome', 'primary ciliary dyskinesia type 1', 'primary ciliary dyskinesia caused by mutation in DNAI1', 'PCD', 'dextrocardia, bronchiectasis, and sinusitis']",0110594,244400,98861,,,C128117,,,,,,
mondo:0009485,"oculocerebrofacial syndrome, Kaufman type","['BPIDS', 'severe mental retardation, microcephaly, long narrow face, ocular anomalies, and long thin hands and feet', 'kos', 'blepharophimosis-ptosis-intellectual disability syndrome', 'KOS', 'severe intellectual disability, microcephaly, long narrow face, ocular anomalies, and long thin hands and feet', 'Kaufman oculocerebrofacial syndrome']",0111456,244450,2707,C1855663,"['0.1992', '-0.2461', '0.2646', '-0.2335', '0.512', '0.1465', '-0.261', '1.108', '-0.8325', '-0.8115', '0.009026', '-0.3213', '-0.261', '-0.3777', '-0.0863', '0.07526', '0.6045', '-0.579', '-0.4468', '-0.1034', '0.2284', '0.2966', '-0.2191', '0.2183', '0.544', '-0.46', '0.02402', '0.5', '0.3723', '-0.2024', '0.517', '-0.1779', '0.4373', '0.4224', '0.194', '-0.498', '-0.2537', '-0.0691', '0.04565', '-0.2874', '0.1488', '0.07544', '0.10876', '0.2019', '-0.00579', '-0.5693', '-0.1359', '0.3398', '-0.339', '-0.175', '-0.1263', '-0.2783', '-0.3506', '-0.2133', '-0.6104', '0.2036', '-0.06067', '0.02406', '0.1328', '-0.2593', '0.1592', '0.4368', '-0.4897', '-0.04868', '-0.1262', '0.2498', '0.5146', '0.2917', '-0.4102', '0.2585', '-0.1378', '0.2036', '-0.2384', '-0.12', '-0.4136', '-0.3022', '0.5903', '-0.05002', '-0.6665', '-0.03375', '0.3347', '-0.206', '0.01085', '0.5186', '-0.2788', '0.6104', '-0.1462', '0.422', '0.5103', '0.7065', '-0.1411', '0.263', '-0.436', '0.4407', '0.3962', '-0.11926', '0.0003376', '-0.2375', '0.581', '0.3147']",,,C537013,,,,
mondo:0009486,autosomal recessive Kenny-Caffey syndrome,"['Kenny-Caffey syndrome type 1', 'Kcs', 'Kenny-Caffey syndrome, type 1', 'Kenny-Caffey syndrome, autosomal recessive', 'KCS1']",0080722,244460,93324,C1855648,"['-0.451', '0.592', '0.8315', '-0.7505', '0.1307', '0.04068', '-0.2474', '0.4475', '-0.7397', '-0.7607', '-0.4365', '0.3135', '-0.1417', '-0.4106', '-0.1127', '0.0467', '0.443', '-0.1744', '-0.0662', '-0.5347', '0.1709', '-0.2913', '0.2825', '-0.10315', '0.1359', '0.279', '0.0475', '0.3083', '0.673', '-0.3816', '-0.426', '0.04547', '0.1478', '-0.04184', '-0.000763', '-0.2852', '0.0358', '0.167', '0.2869', '-0.3345', '0.1927', '-0.2245', '0.2874', '-0.03043', '0.3347', '-0.8486', '0.3018', '0.4788', '0.4932', '-0.1335', '0.01044', '0.05484', '-0.1724', '0.1065', '-0.59', '-0.617', '-0.1858', '0.2524', '-0.3838', '0.2722', '0.05927', '-0.2527', '-0.402', '-0.2064', '0.3896', '0.1079', '0.2039', '0.3657', '-0.4998', '0.1061', '-0.5527', '-0.0746', '0.557', '-0.275', '-0.333', '0.3533', '0.4429', '0.1053', '-0.01988', '0.4348', '-0.3176', '0.2944', '-0.01501', '-0.06824', '-0.184', '-0.07465', '-0.02184', '0.2294', '0.658', '0.4668', '-0.5786', '0.531', '-0.0796', '-0.11255', '0.4924', '0.2029', '0.6816', '-0.632', '0.46', '0.3337']",C130992,,C537021,,,,
mondo:0009487,keratoconus and congenital hip dysplasia,['keratoconus and congenital hip dysplasia'],,244510,,C1855647,,,,C565456,,,,
mondo:0009488,keratoconus posticus circumscriptus,"['Kpc with associated malformations', 'KPC', 'keratoconus posticus CIRCUMSCRIPTUS', 'keratoconus posticus circumscriptus']",,244600,,C1855645,,,,C536151,,,,
mondo:0009489,"hereditary palmoplantar keratoderma, Gamborg-Nielsen type","['palmoplantar keratoderma, Norrbotten recessive type', 'PPKNR', 'PPK, Gamborg-Nielsen type', 'hereditary palmoplantar hyperkeratosis, Gamborg-Nielsen type']",,244850,86923,,,,,C565454,,,,
mondo:0009490,Papillon-Lefevre disease,"['palmar-plantar hyperkeratosis and concomitant periodontal destruction', 'PALS', 'Papillon Lefevre syndrome', 'keratosis palmoplantar - periodontopathy', 'PLS', 'hyperkeratosis palmoplantaris with periodontosis', 'palmoplantar keratoderma with periodontosis', 'Keratoris palmoplantaris with periodontopathia', 'Papillon-Lefvre syndrome', 'PAPILLON-Lefevre syndrome', 'Papillon-LEFèvre syndrome', 'keratosis palmoplantaris with periodontopathia', 'Pls', 'keratosis palmoplantar-periodontopathy syndrome']",3389,245000,678,C0030360,"['0.221', '0.0563', '-0.09', '-0.4739', '0.608', '-0.558', '0.253', '0.562', '0.1134', '0.06476', '-0.3008', '-0.2229', '-0.2554', '-0.0836', '-0.2329', '-0.3096', '0.2656', '-0.5225', '-0.2073', '-0.999', '-0.4338', '-0.1948', '0.7427', '-0.8228', '0.09595', '0.2676', '-0.5117', '0.578', '-0.341', '-0.769', '-0.05225', '0.2964', '-0.3418', '-0.2335', '0.4668', '0.0547', '0.0738', '-0.407', '0.1028', '0.2015', '-0.2262', '-0.3118', '0.1919', '0.01694', '-0.1422', '0.0771', '-0.4736', '0.0883', '0.516', '-0.387', '0.10846', '-0.029', '0.5913', '-0.04837', '-0.2905', '0.05118', '0.8813', '-0.61', '-0.2988', '-0.3608', '0.1477', '0.4963', '-0.595', '-0.192', '0.301', '-0.2491', '0.335', '0.4841', '0.226', '0.7446', '-0.296', '-0.87', '-0.1954', '0.1904', '0.3757', '0.003347', '-0.3406', '0.4062', '0.1268', '-0.309', '-0.1026', '0.1181', '0.3506', '0.1395', '0.31', '0.1123', '0.2302', '0.1354', '0.5283', '0.906', '0.0649', '-0.1783', '0.02513', '0.8003', '-0.07605', '0.4297', '0.6357', '-0.731', '-0.0785', '-0.1583']",C84992,,D010214,759.89,,,
mondo:0009491,Haim-Munk syndrome,"['HMS', 'HAIM-Munk syndrome', 'Haim-Munk syndrome', 'keratosis palmoplantaris-periodontopathia-onychogryposis syndrome', 'keratosis palmoplantaris with periodontopathia and onychogryposis', 'Cochin Jewish disorder', 'palmoplantar hyperkeratosis-periodontopathia-onychogryposis syndrome', 'palmoplantar keratoderma-periodontopathia-onychogryposis syndrome']",,245010,2342,C1855627,"['-0.03458', '0.1298', '-0.1572', '-0.1898', '0.01602', '-0.6006', '-0.098', '-0.06964', '-0.3533', '0.2408', '-0.3262', '-0.271', '-0.2219', '0.1993', '-0.432', '0.10406', '0.3777', '-0.078', '-0.2354', '-0.3132', '-0.03186', '-0.0237', '0.1367', '-1.197', '-0.158', '0.4507', '-0.7144', '0.716', '-0.0901', '-0.8315', '0.1176', '-0.004322', '-0.2898', '0.773', '0.4675', '-0.624', '-0.04047', '-0.6855', '0.1505', '-0.2883', '-0.5264', '-1.092', '-0.3784', '0.1273', '-0.0924', '-0.3794', '-0.0738', '0.2355', '-0.216', '-0.514', '-0.1902', '0.1592', '0.4724', '0.4172', '0.144', '-0.469', '0.7974', '-0.2361', '-0.2363', '-0.000807', '0.6753', '-0.09564', '-0.3533', '0.06805', '0.07227', '0.3376', '0.458', '0.81', '0.09766', '0.548', '-0.764', '-0.53', '0.2091', '0.0852', '0.2363', '0.379', '-0.09875', '0.5225', '0.696', '-0.11774', '-0.1409', '0.2273', '0.03091', '0.825', '0.1986', '0.674', '-0.377', '0.549', '0.04483', '0.2778', '0.00824', '-0.1177', '-0.311', '0.7334', '0.1641', '-0.04135', '0.7407', '-1.169', '0.7876', '-0.634']",,,C537627,,,,
mondo:0009492,succinyl-CoA:3-ketoacid CoA transferase deficiency,"['succinyl-CoA:3-oxoacid CoA transferase deficiency', 'succinyl-CoA:3-oxoacid-CoA transferase deficiency', 'OXCT1 deficiency', 'SCOTD', 'succinyl-Coa:3-ketoacid Coa-transferase deficiency', '3-oxoacid CoA transferase deficiency', 'succinyl-Coa:acetoacetate transferase deficiency', 'SCOT deficiency', 'succinyl-CoA acetoacetate transferase deficiency', 'ketoacidosis due to Scot deficiency', 'Scot deficiency', 'Succinyl CoA:3-oxoacid CoA transferase deficiency']",,245050,832,,"['-0.07416', '0.384', '-0.721', '0.2632', '-0.0718', '-0.4568', '-0.2693', '0.5703', '0.191', '-0.498', '-0.4548', '-0.08075', '0.5625', '0.4958', '-0.5376', '-0.3354', '-0.08844', '0.1548', '-0.8003', '-1.268', '-0.259', '-0.1864', '0.519', '-0.4001', '-0.1111', '-0.4836', '-0.11383', '0.4858', '0.0614', '-0.2522', '0.6987', '0.2854', '0.3552', '0.1982', '-0.697', '-0.11273', '0.3545', '0.2522', '-0.06903', '-0.08203', '-0.08295', '-0.3147', '0.0889', '-0.2415', '0.03577', '0.01168', '-0.03802', '-0.8296', '-0.4438', '0.9336', '-0.2893', '-0.4507', '0.5396', '-0.10034', '-0.02982', '0.2927', '0.2976', '0.09406', '0.2118', '0.2727', '0.513', '0.1742', '0.4314', '-0.2375', '0.1322', '0.1437', '-0.01208', '0.349', '-0.7744', '0.1068', '-0.05392', '0.3318', '-0.269', '-0.1874', '0.4617', '0.752', '0.145', '-0.1301', '-0.3188', '0.2069', '0.11273', '-0.4666', '0.1417', '-0.0884', '0.813', '0.865', '-0.1882', '0.07166', '0.3687', '0.3354', '0.857', '-0.2218', '-0.5664', '0.282', '-0.08875', '0.465', '-0.0996', '-0.1626', '-0.4463', '0.2189']",,,C537527,270.8,,,
mondo:0009493,Richards-Rundle syndrome,"['ataxia-deafness-intellectual disability syndrome', 'ataxia-deafness-mental retardation syndrome', 'familial ataxia-hypogonadism syndrome', 'ataxia-deafness-retardation syndrome with ketoaciduria', 'ketoaciduria-intellectual disability-ataxia-deafness syndrome', 'Richards-Rundle syndrome', 'ketoaciduria - intellectual disability - ataxia - deafness', 'RRNS', 'ketoaciduria-mental deficiency syndrome', 'RICHARDS-RUNDLE syndrome']",,245100,1399,C0796136,,,,C535674,,,,
mondo:0009495,Keutel syndrome,"['Keutel syndrome', 'pulmonic stenosis, brachytelephalangism, and calcification of cartilages', 'KEUTEL syndrome', 'KTLS', 'pulmonic stenosis-brachytelephalangism-calcification of cartilages syndrome', 'pulmonic stenosis brachytelephalangism and calcification of cartilages']",,245150,85202,C1855607,"['0.0806', '0.4731', '0.1332', '-1.084', '-0.1578', '-0.3604', '0.6885', '0.595', '-0.2394', '-0.318', '-0.654', '-0.3044', '0.08295', '-0.2438', '-0.2217', '0.3704', '0.2477', '-0.05127', '-0.5376', '-0.2155', '0.3176', '-0.4255', '0.1748', '-0.2443', '-0.1103', '-0.1898', '-0.318', '0.08', '0.833', '-0.4314', '0.1823', '-0.2737', '-0.183', '-0.8887', '0.2135', '-0.2688', '-0.1718', '-0.57', '0.231', '-0.3262', '-0.1167', '-0.2054', '0.571', '-0.02403', '-0.04077', '0.2028', '-0.0827', '-0.166', '-0.3098', '-0.3752', '-0.2064', '0.2112', '0.349', '0.7144', '0.004955', '-0.5815', '0.2717', '0.02597', '0.3726', '0.1991', '-0.178', '0.5254', '-0.02477', '0.1832', '-0.2477', '-0.724', '0.3494', '0.8', '-0.3562', '0.559', '-0.3406', '0.537', '0.0792', '0.11646', '-0.0802', '0.2769', '0.5337', '0.765', '0.199', '0.0529', '0.229', '-0.2393', '0.473', '0.8784', '-0.502', '0.364', '0.1476', '0.8555', '-0.1698', '0.503', '-0.05057', '0.6255', '0.2664', '0.55', '1.137', '-0.01018', '0.736', '-0.625', '0.1378', '-0.2443']",,,C536167,,,,
mondo:0009496,Kniest-like dysplasia with pursed lips and ectopia lentis,"['burton syndrome', 'Kniest-like dysplasia with pursed lips and ectopia lentis']",,245160,,C1855606,,,,,,,,
mondo:0009497,Kifafa seizure disorder,"['Vitsala', 'parkinsonian features and neurologic abnormalities, intellectual disability and transient psychotic episodes', 'Kifafa seizure disorder', 'Complex familial seizure disorder', 'parkinsonian features and neurologic abnormalities, mental retardation and transient psychotic episodes']",,245180,,C0796010,,,,C537708,,,,
mondo:0009498,lethal Kniest-like dysplasia,"['arthrosis, flat face, hypotonia, short neck and macrocephaly', 'Kniest-like dysplasia, lethal', 'Kniest like dysplasia lethal']",,245190,2347,C1855605,,,,C537208,,,,
mondo:0009499,Krabbe disease,"['Krabbe^s disease', 'beta galactocerebrosidase deficiency', 'galactosylceramide Beta-galactosidase deficiency', 'Krabbe^s leukodystrophy', 'globoid cell leukoencephalopathy', 'galactosylceramidase deficiency', 'globoid cell leukodystrophy', 'Krabbe leukodystrophy', 'GALC deficiency', 'GLD', 'diffuse globoid body sclerosis', 'Krabbe disease', 'galactosylceramide lipidosis', 'galactocerebrosidase deficiency']",10587,245200,487,C0023521,"['-0.003428', '0.4604', '-0.06207', '0.3506', '-0.01918', '-0.2932', '-0.2727', '1.053', '-0.164', '-0.2556', '0.21', '-0.5386', '0.03094', '0.4065', '0.3545', '-0.2856', '-0.9546', '-0.614', '-0.2827', '-0.1952', '-0.4329', '-0.6265', '0.0986', '-0.3967', '-0.1635', '-0.8413', '-0.1436', '0.2856', '-0.1428', '-0.1389', '0.1108', '-0.0494', '0.6123', '0.266', '-0.3137', '0.3616', '-0.4133', '0.3552', '-0.10583', '-0.32', '0.3726', '-0.0664', '0.0769', '0.47', '-0.2253', '-0.1338', '-0.02502', '-0.833', '0.0106', '0.763', '0.3606', '-0.0002856', '-0.2595', '-0.4956', '0.1279', '-0.836', '-0.0479', '0.1947', '0.1998', '-0.12354', '0.08826', '0.1256', '0.7983', '0.569', '-0.0692', '0.5933', '-0.2367', '0.2559', '-0.3901', '0.2119', '0.282', '-0.1451', '0.048', '-0.2683', '0.553', '-0.1169', '0.01507', '0.465', '0.4749', '-0.2007', '0.4495', '-0.6675', '0.02559', '0.271', '-0.1582', '-0.294', '0.3374', '0.3296', '0.696', '0.541', '0.5586', '-0.1407', '-0.693', '0.069', '0.2197', '0.2898', '0.3135', '-1.033', '0.281', '0.03047']",C61254,,D007965,,E75.23,10023492,
mondo:0009500,"kuru, susceptibility to","['susceptibility to kuru', 'kuru, susceptibility to']",,245300,,C1855588,,,,,,,,
mondo:0009501,metabolic myopathy due to lactate transporter defect,"['lactate transporter defect, myopathy due to', 'erythrocyte lactate transporter defect']",,245340,171690,C1855577,"['-0.649', '-0.1339', '-0.0872', '-0.0797', '0.2025', '-0.4426', '-0.0658', '0.5273', '-0.2229', '0.03522', '-0.0559', '0.3167', '0.3523', '-0.04166', '-0.292', '0.3108', '-0.01503', '-0.0823', '-0.494', '-0.6475', '0.3684', '-0.2693', '0.02838', '0.3298', '-0.1283', '0.005013', '0.2002', '-0.1451', '-0.284', '-0.3542', '0.1342', '0.2341', '0.341', '0.1868', '-0.2937', '-0.349', '-0.0834', '-0.12305', '0.1027', '-0.3608', '-0.1566', '-0.2998', '0.2668', '0.3977', '-0.3552', '0.03494', '0.1085', '0.2703', '0.2192', '0.5327', '-0.4055', '-0.3403', '0.2142', '0.07916', '0.01462', '-0.2646', '0.4475', '-0.3599', '-0.2566', '-0.11145', '0.516', '0.448', '0.12054', '-0.372', '-0.284', '0.4207', '0.466', '0.4968', '-0.4514', '-0.02129', '-0.1715', '0.01889', '0.165', '0.01495', '0.3157', '0.2288', '0.2898', '0.00888', '0.0842', '0.279', '0.1929', '0.1588', '0.2389', '-0.1108', '-0.0768', '0.3164', '0.0742', '0.5874', '0.5327', '-0.1753', '0.501', '0.004215', '0.2327', '-0.03885', '0.3987', '0.3455', '0.2252', '-0.3657', '-0.3713', '0.0955']",,,C565449,,,,
mondo:0009502,pyruvate dehydrogenase E2 deficiency,"['PDHDD', 'dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex deficiency', 'lactic acidemia due to defect of E2 lipoyl transacetylase of the pyruvate dehydrogenase Complex', 'dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex deficiency', 'pyruvate dehydrogenase complex component E2 deficiency', 'pyruvate dehydrogenase E2 deficiency']",,245348,79244,C1855565,"['-0.8438', '0.2896', '-0.1466', '-0.1304', '0.1587', '-0.2069', '-0.3203', '0.5674', '-0.0533', '0.042', '-0.3848', '-0.1289', '0.1692', '0.2407', '0.2761', '0.0782', '0.03796', '-0.287', '-0.4229', '-0.9023', '-0.3035', '-0.2177', '0.611', '0.03363', '-0.1283', '0.1581', '-0.485', '0.02531', '-0.391', '-0.03458', '0.1829', '0.236', '0.1769', '0.5024', '-0.1394', '0.1622', '-0.2576', '-0.08167', '-0.1353', '0.4573', '0.2399', '-0.6094', '0.0817', '-0.008766', '0.04224', '0.01875', '0.2725', '0.3696', '0.0908', '0.1947', '0.1141', '0.0766', '-0.3445', '-0.01083', '0.04233', '0.1223', '0.3772', '-0.6387', '-0.1753', '0.7925', '0.03894', '-0.03363', '0.4028', '0.0587', '-0.04678', '0.0581', '0.4602', '0.2339', '-0.269', '0.4756', '0.02353', '0.10175', '-0.02213', '-0.148', '0.2368', '0.542', '0.05945', '-0.01752', '-0.346', '0.09283', '0.245', '-0.4158', '0.0867', '0.1635', '0.5176', '0.128', '0.04794', '-0.1956', '0.8154', '-0.1236', '0.6914', '0.3948', '-0.28', '0.004112', '0.425', '0.495', '0.37', '-0.0218', '0.1858', '0.2471']",,,C565448,,,,
mondo:0009503,pyruvate dehydrogenase E3-binding protein deficiency,"['2-oxoglutarate complex deficiency', 'lactic acidemia due to defect in lipoyl-containing component 10 of the pyruvate dehydrogenase Complex', 'Glycine cleavage system L protein deficiency', 'pyruvate dehydrogenase E3-binding PROTEIN deficiency', 'branched chain alpha-ketoacid dehydrogenase complex deficiency', 'PDHXD', 'pyruvate dehydrogenase E3-binding protein deficiency', 'pyruvate dehydrogenase protein X component deficiency', 'lacticacidemia due to PDX1 deficiency', 'lipoamide dehydrogenase deficiency', 'diaphorase deficiency', 'dihydrolipoyl dehydrogenase deficiency', 'pyruvate dehydrogenase complex component E3 deficiency']",,245349,255182,C1855553,"['-0.5234', '0.2607', '-0.1844', '0.1493', '0.0706', '-0.2172', '-0.2603', '0.6167', '0.1519', '-0.0856', '-0.4854', '-0.4316', '-0.1508', '-0.10114', '-0.11224', '-0.2161', '-0.063', '-0.4075', '-0.409', '-0.524', '-0.2019', '-0.0883', '0.9644', '0.156', '0.2004', '0.187', '-0.4275', '0.2764', '-0.009834', '-0.01316', '0.01503', '-0.074', '0.4187', '0.1462', '-0.04242', '-0.262', '-0.3337', '-0.1504', '-0.1718', '0.2988', '0.5054', '-0.4211', '0.08636', '0.09424', '0.2883', '-0.2418', '0.1475', '0.304', '0.165', '0.0742', '0.2474', '-0.15', '-0.633', '-0.07623', '-0.606', '0.1158', '0.4753', '-0.5786', '-0.2485', '0.708', '0.01397', '0.0935', '0.5503', '-0.0564', '-0.0818', '0.1385', '0.3784', '0.4072', '-0.4575', '0.4775', '0.3108', '0.2646', '0.03967', '-0.266', '0.2542', '0.5234', '0.2656', '-0.2534', '-0.1562', '0.5127', '0.5054', '-0.1642', '0.0643', '0.00997', '0.67', '0.0221', '0.1749', '-0.04605', '0.7974', '-0.1151', '0.6587', '0.617', '-0.2607', '-0.11566', '0.4106', '0.525', '0.2253', '-0.3716', '0.3218', '0.2085']",,,C565447,,,,
mondo:0009504,mitochondrial DNA depletion syndrome 9,"['mitochondrial DNA depletion syndrome type 9', 'mitochondrial DNA depletion syndrome caused by mutation in SUCLG1', 'succinate-CoA ligase deficiency', 'fatal infantile lactic acidosis with methylmalonic aciduria', 'MTDPS9', 'lactic acidosis congenital infantile', 'lactic acidosis, fatal infantile, formerly', 'SUCLG1 mitochondrial DNA depletion syndrome', 'mitochondrial DNA depletion syndrome 9 (encephalomyopathic type with methylmalonic aciduria)', 'lactic acidosis, fatal infantile']",0080128,245400,17,,"['-0.2551', '-0.07025', '-0.0978', '0.154', '-0.1335', '-0.296', '-0.2825', '0.5625', '-0.1309', '-0.1301', '-0.3977', '-0.444', '-0.03061', '0.1417', '-0.0644', '0.07495', '-0.2274', '-0.2074', '-0.452', '-0.7603', '0.4072', '-0.2372', '0.4797', '0.0412', '0.05692', '-0.4', '0.0938', '-0.05014', '-0.007698', '0.079', '0.07336', '-0.0827', '0.521', '0.4626', '-0.1637', '0.3096', '-0.4143', '-0.004482', '-0.2952', '0.12177', '0.3787', '-0.3782', '0.2983', '0.05078', '-0.1483', '-0.3599', '-0.1199', '0.02574', '-0.2688', '0.5186', '-0.211', '-0.2013', '0.4207', '-0.4045', '0.2391', '-0.313', '0.286', '-0.1694', '-0.155', '0.3745', '0.1844', '-0.08936', '0.7373', '-0.1857', '-0.0479', '-0.04803', '0.3738', '0.1039', '-0.4375', '0.1324', '-0.09717', '0.3774', '-0.2979', '0.0778', '-0.1523', '-0.1312', '0.4766', '-0.327', '-0.392', '0.2362', '-0.485', '0.3435', '-0.1807', '0.01187', '0.3948', '0.1222', '0.0861', '-0.12103', '0.2854', '-0.1388', '0.5967', '0.2323', '-0.01839', '-0.02145', '0.2367', '0.55', '0.1843', '-0.2355', '0.1501', '0.00737']",,,C566885,,,,
mondo:0009505,lactic aciduria due to D-lactic acid,"['D-lactic aciduria with susceptibility to gout', 'lactic aciduria due to D-lactic acid']",,245450,,C1855552,"['-0.06366', '0.07513', '0.0185', '0.00686', '0.03534', '-0.0743', '-0.02766', '0.1008', '-0.05988', '0.0154', '-0.03912', '-0.01918', '0.006023', '-0.00666', '-0.03047', '-0.02747', '-0.007023', '-0.04007', '-0.05472', '-0.1316', '-0.02739', '-0.05594', '0.0611', '-0.01585', '0.01267', '-0.02446', '-0.01352', '-0.01376', '-0.001639', '-0.0196', '0.042', '0.005978', '0.07056', '0.0438', '-0.01643', '-0.02885', '-0.02791', '-0.02754', '-0.02449', '-0.04245', '0.02191', '-0.1028', '0.02466', '-0.01236', '-0.041', '-0.05167', '0.004585', '0.04642', '0.01078', '0.01869', '-0.04974', '-0.0272', '0.010735', '-0.001951', '-0.03143', '-0.01219', '0.07806', '-0.03812', '-0.0813', '0.02858', '0.05853', '0.02242', '0.0555', '-0.01283', '0.01148', '0.00357', '0.10406', '0.05554', '-0.0649', '0.08307', '-0.04697', '0.01898', '-0.01042', '-0.03824', '0.03214', '0.0604', '0.03552', '-0.03522', '-0.03117', '-0.00688', '0.004894', '-0.0105', '-0.02338', '0.04993', '0.015434', '0.02287', '0.02878', '0.05145', '0.10254', '0.01697', '0.0523', '0.0472', '-0.01962', '0.0001004', '0.11536', '0.0675', '0.05087', '-0.08356', '-0.01284', '0.03156']",,,C565446,,,,
mondo:0009506,specific granule deficiency,"['lactoferrin-deficient neutrophils', 'neutrophil-specific granule deficiency', 'neutrophil lactoferrin deficiency', 'SGD', 'specific granule deficiency', 'recurrent infection due to specific granule deficiency']",,,169142,C0398593,"['-0.4448', '-0.1029', '0.417', '-0.3867', '0.09045', '-0.07635', '0.1549', '0.2043', '-0.07916', '0.04645', '-0.2284', '-0.0883', '-0.01401', '-0.04837', '-0.09705', '0.1654', '-0.05185', '-0.03976', '-0.0566', '-0.3643', '0.2461', '-0.212', '0.3184', '-0.1217', '0.1278', '-0.0568', '0.0275', '0.1904', '-0.07947', '-0.1942', '0.02988', '0.425', '0.1855', '0.0654', '0.1879', '-0.004448', '-0.533', '-0.1318', '0.0397', '-0.4395', '-0.0563', '0.02518', '0.1045', '-0.11426', '-0.335', '-0.4697', '0.02556', '0.2086', '0.08655', '-0.1672', '-0.09265', '0.1288', '0.2754', '0.4023', '-0.3691', '-0.1722', '0.0785', '-0.3816', '-0.255', '0.07983', '-0.01736', '0.2118', '-0.517', '-0.2025', '0.257', '-0.0267', '0.2451', '0.4907', '-0.25', '0.4612', '-0.10846', '-0.0438', '-0.1268', '-0.0935', '-0.0786', '-0.06238', '0.5073', '-0.0844', '0.1547', '-0.1008', '-0.3142', '-0.309', '-0.2052', '0.2286', '-0.295', '0.02982', '0.0785', '0.3052', '0.1254', '-0.1139', '0.338', '0.388', '-0.1043', '0.11444', '0.4888', '0.368', '0.355', '-0.082', '0.2556', '-0.014404']",,,C562873,,,,
mondo:0009507,Lambert syndrome,"['Lambert syndrome', 'branchial dysplasia clubfoot inguinal hernia and biliary atresia', 'branchial dysplasia, clubfoot, inguinal hernia, and biliary atresia', 'branchial dysplasia-intellectual disability-inguinal hernia syndrome']",,245550,1296,C1855551,,,,C538396,,,,
mondo:0009508,Lambotte syndrome,"['microcephaly, holoprosencephaly, and intrauterine Growth retardation', 'Lambotte syndrome']",,245552,,C1855550,,,,C537549,,,,
mondo:0009509,Landau-Kleffner syndrome,"['aphasia, acquired, with epilepsy', 'Rolandic epilepsy, intellectual disability, and speech dyspraxia, autosomal dominant', 'epilepsy, focal, with speech disorder and with or without mental retardation', 'Rolandic epilepsy, mental retardation, and speech dyspraxia, autosomal dominant', 'acquired epileptic aphasia', 'acquired epileptiform aphasia', 'LKS', 'epilepsy, focal, with speech disorder and with or without intellectual disability', 'acquired aphasia with convulsive disorder', 'benign epilepsy of childhood with centrotemporal spikes', 'continuous Spike and waves during slow-Wave sleep syndrome', 'Landau-Kleffner syndrome', 'epilepsy, focal, with speech disorder and with or without impaired intellectual development', 'FESD']",2538,245570,98818,C0282512,"['0.866', '0.443', '0.1915', '-0.3298', '-0.667', '-0.2727', '1.001', '0.827', '-0.5845', '-0.4512', '-0.3767', '0.3794', '-0.1383', '-0.1655', '0.644', '-0.02357', '-0.4573', '0.07385', '-0.2494', '-0.4387', '0.2181', '0.1483', '0.1013', '-0.06195', '0.2062', '0.04544', '-0.594', '-0.2559', '-0.386', '0.3745', '1.04', '-0.08673', '0.3083', '0.445', '-0.04706', '0.3496', '0.2517', '-0.5054', '0.3071', '-0.5796', '0.466', '-0.4265', '0.012115', '-0.1', '1.097', '-0.166', '-0.4358', '0.00589', '0.3198', '0.755', '0.1826', '0.3118', '-0.181', '-0.4004', '0.4392', '0.1357', '0.2944', '0.146', '-0.4736', '0.2683', '0.1356', '0.316', '0.979', '0.1881', '-0.256', '-0.04184', '0.2445', '-0.425', '0.06235', '0.5435', '-0.3232', '-0.06445', '-0.2742', '0.03568', '0.4353', '0.1383', '0.3545', '-0.0728', '-0.508', '-0.1626', '0.1826', '0.4382', '-0.2351', '-0.0996', '-0.4421', '0.3794', '0.3674', '0.3767', '0.311', '0.11426', '0.02592', '0.725', '-0.2625', '0.475', '0.05392', '0.00209', '0.2422', '-0.4858', '0.1278', '0.02617']",C84806,1001010,D018887,,,10052083,
mondo:0009511,"Larsen-like syndrome, B3GAT3 type","['multiple Joint dislocations, short stature, and craniofacial Dysmorphism with or without congenital heart defects', 'Larsen syndrome, autosomal recessive', 'multiple joint dislocations, short stature, craniofacial dysmorphism, with or without congenital heart defects', 'multiple JOINT dislocations, short stature, craniofacial dysmorphism, and congenital heart defects', 'Larsen syndrome, autosomal recessive, formerly', 'JDSCD', 'multiple joint dislocations-short stature-craniofacial dysmorphism-congenital heart defects syndrome', 'multiple JOINT dislocations, short stature, and craniofacial dysmorphism with or without congenital heart defects']",0080575,245600,284139,,"['-0.1982', '-0.2336', '0.5474', '-0.1553', '0.1145', '-0.2312', '0.04694', '0.418', '-0.5586', '-0.1074', '-0.06805', '-0.09534', '-0.0928', '-0.108', '-0.4617', '0.2288', '0.4736', '-0.05798', '0.1092', '-0.3623', '0.03494', '0.08685', '0.2612', '-0.114', '0.05237', '0.0956', '-0.114', '0.1251', '0.3904', '-0.2598', '0.1453', '-0.2986', '0.608', '0.5146', '0.3132', '-0.3882', '-0.03748', '-0.4229', '-0.1879', '-0.6094', '0.05115', '-0.2013', '0.1824', '-0.0781', '0.0135', '-0.2861', '0.1143', '0.87', '0.0339', '0.0392', '-0.3306', '0.1732', '0.1466', '0.0353', '-0.2512', '-0.455', '-0.1885', '-0.3381', '0.0373', '0.0472', '0.3904', '-0.1368', '-0.4033', '0.2642', '-0.0746', '-0.00919', '0.0952', '0.4468', '-0.1901', '0.2942', '-0.3525', '0.201', '-0.001218', '-0.2837', '-0.1404', '0.06494', '-0.1475', '-0.3127', '-0.3', '0.03555', '0.08997', '0.0349', '-0.0684', '0.8584', '-0.2487', '0.0556', '-0.166', '0.3901', '0.10657', '0.1315', '-0.2451', '0.2651', '0.1328', '0.1475', '0.664', '0.2091', '0.649', '-0.2097', '0.3992', '0.1412']",,,C537874,,,,
mondo:0009512,lethal Larsen-like syndrome,"['Larsen-like syndrome, lethal type', 'Larsen-like multiple joint dislocation syndrome']",,245650,2371,C4304741,,,,C537872,,,,
mondo:0009513,laryngo-onycho-cutaneous syndrome,"['LOC syndrome', 'laryngo-onycho-cutaneous syndrome', 'LOCS', 'laryngeal and ocular granulation tissue in children from the Indian subcontinent syndrome', 'logic syndrome', 'LARYNGOONYCHOCUTANEOUS syndrome', 'Shabbir syndrome']",,245660,2407,C1328355,"['0.0759', '0.4456', '-1.3', '-0.636', '-0.2289', '-0.4517', '0.1296', '0.1874', '-0.2228', '-0.641', '-0.1558', '-0.559', '-0.946', '-0.466', '-0.05405', '0.1816', '0.459', '-0.5596', '0.01869', '-0.9956', '-0.4614', '-0.2007', '0.788', '-0.01316', '0.3608', '0.1697', '-0.3604', '0.4463', '-0.005524', '-0.1423', '0.2449', '-0.01132', '-0.375', '0.412', '-0.0288', '0.1195', '-0.007904', '-0.1085', '-0.3015', '-0.2299', '-0.1364', '-0.377', '-0.2737', '-0.03156', '-0.12445', '-0.0371', '-0.2162', '0.3179', '0.3936', '-0.1625', '-0.4766', '-0.3997', '0.0825', '-0.07715', '-0.668', '-0.7456', '0.7124', '0.6016', '0.417', '-0.1254', '0.1564', '0.1108', '-0.12396', '0.1803', '0.03214', '-0.8145', '0.04813', '0.653', '-0.623', '0.743', '-0.4795', '-0.1617', '-0.3914', '0.5176', '-0.2473', '0.2705', '0.0528', '0.311', '-0.0451', '0.3142', '-0.676', '0.0852', '0.321', '-0.4504', '-0.1719', '0.2832', '-0.00953', '0.4297', '0.2261', '-0.951', '-0.0681', '0.1777', '-0.4683', '0.3948', '1.032', '0.514', '0.681', '-0.4314', '0.00839', '0.4185']",,,C537032,,,,
mondo:0009514,Laurence-Moon syndrome,"['LNMS', 'Laurence-MOON syndrome', 'Laurence-Moon-Biedl syndrome', 'Laurence-Moon syndrome', 'LMS']",1930,245800,2377,C0023138,"['-0.7285', '0.06714', '-0.2318', '-0.2194', '-0.4683', '-0.809', '-0.2947', '0.377', '-0.471', '-0.05508', '-0.3616', '-0.591', '-0.1538', '-0.232', '0.584', '-0.2615', '0.2507', '0.2876', '-0.1204', '-0.8003', '-0.06757', '-0.01523', '-0.0873', '-0.3093', '-0.0585', '0.2211', '-0.3376', '-0.1975', '0.2074', '-0.01593', '0.5874', '0.0468', '-0.01546', '0.262', '-0.2703', '-0.3713', '0.1625', '-0.1677', '-0.3472', '0.005642', '0.0008397', '-0.3154', '0.3835', '0.11774', '0.3633', '-0.7393', '0.1628', '-0.1682', '-0.001812', '-0.548', '0.04495', '0.438', '-0.07043', '0.01511', '0.1324', '-0.185', '0.7754', '-0.1073', '-0.2279', '0.543', '-0.00298', '-0.1252', '0.356', '0.05908', '-0.317', '0.1426', '0.0673', '0.8994', '-0.7725', '0.628', '-0.833', '-0.003717', '0.3286', '-0.1195', '0.7134', '-0.3794', '-0.1065', '-0.1575', '0.1342', '0.07776', '0.4746', '0.2622', '-0.626', '0.961', '-0.3755', '-0.1061', '0.3162', '0.1865', '0.1974', '0.1947', '0.4639', '0.2983', '-0.1991', '0.0378', '0.4663', '0.2722', '0.5273', '0.1611', '0.586', '0.4792']",C34760,,D007849,253.4,,10056710,
mondo:0009515,Norum disease,"['lecithin:cholesterol acyltransferase deficiency', 'LCAT deficiency', 'Norum disease', 'lecithin acyltransferase deficiency', 'familial LCAT deficiency', 'complete LCAT deficiency', 'FLD']",1391,245900,79293,CN205883,"['-0.375', '0.2607', '-0.2795', '0.0759', '0.509', '-0.2079', '-0.925', '0.6885', '0.153', '-1.084', '-0.04074', '-0.5093', '-0.11865', '0.2437', '-0.2532', '-0.814', '0.6743', '-0.303', '0.2019', '-0.6714', '0.2317', '0.04227', '0.6406', '0.1567', '0.2201', '0.624', '0.302', '0.1268', '-0.03053', '-0.11334', '0.8394', '0.0751', '0.8384', '0.1791', '-0.03087', '-0.464', '-0.3086', '-0.8896', '0.1079', '-0.09656', '-0.09204', '0.345', '0.8716', '-0.3572', '-0.833', '-0.00964', '0.1245', '-0.538', '0.1992', '0.389', '0.4795', '0.3557', '0.6475', '-0.3022', '-0.3281', '0.03003', '0.439', '-0.1783', '-0.4465', '0.2174', '-0.06134', '-0.1727', '0.3572', '-0.694', '0.1141', '-0.578', '0.531', '0.798', '-0.1272', '-0.204', '0.2832', '-0.851', '-0.1522', '0.2964', '0.6426', '0.3245', '0.2656', '-0.1626', '-0.066', '-0.0591', '0.1882', '-0.323', '-0.1578', '0.4988', '0.482', '0.3303', '-0.2391', '-0.2583', '0.8945', '0.2351', '0.4812', '0.1946', '-0.1434', '0.1808', '0.7295', '0.572', '0.512', '-0.5127', '0.1241', '0.7266']",C84813,,,,,,
mondo:0009516,absence deformity of leg-cataract syndrome,"['leg, absence deformity of, with congenital cataract']",,246000,2310,C1855523,,,,C565442,,,,
mondo:0009517,Donohue syndrome,"['Donohue syndrome', 'insulin receptor, defect 1N', 'leprechaunism']",0050470,246200,508,C0271695,"['-0.02797', '0.2766', '-0.2297', '-0.4854', '0.3003', '-0.347', '0.3176', '0.292', '-0.146', '-0.55', '-0.0439', '-0.1985', '0.282', '-0.1818', '-0.709', '0.0922', '0.00197', '0.2888', '0.01241', '-0.933', '0.2512', '-0.5996', '0.7', '-0.4119', '-0.007835', '0.722', '-0.52', '-0.838', '0.1025', '-0.903', '0.939', '0.624', '0.5903', '0.2742', '-0.8657', '0.4307', '-0.2502', '0.02089', '-0.683', '-0.3113', '0.3633', '-0.2266', '-0.5493', '0.1873', '-0.006496', '-0.233', '0.011696', '0.0779', '0.1385', '0.1917', '0.2063', '-0.4456', '0.4434', '-0.10693', '-0.6504', '-0.2413', '0.1345', '-0.4282', '-0.115', '0.2905', '-0.2998', '-0.03757', '-0.2384', '0.07117', '-0.01978', '-0.2288', '-0.1445', '-0.3816', '-0.84', '0.03708', '-0.668', '0.2603', '0.4065', '0.09595', '0.4548', '-0.1748', '-0.4402', '-0.10394', '-0.526', '-0.3455', '0.164', '-0.1713', '-0.4675', '0.1895', '-0.354', '0.2925', '0.3508', '0.1484', '0.462', '0.5107', '0.3162', '0.3674', '0.2161', '-0.2026', '0.482', '0.0621', '0.04855', '-0.625', '0.2213', '0.0398']",C84676,,D056731,259.8,,,
mondo:0009518,"leprosy, susceptibility to, 3","['TLR2 leprosy', 'LPRS3', 'leprosy, susceptibility to, type 3', 'susceptibility to leprosy 3', 'leprosy, susceptibility to, 3', 'leprosy, susceptibility to', 'leprosy caused by mutation in TLR2']",,246300,,,,,,,,,,
mondo:0009519,letterer-Siwe disease,"['acute and disseminated Langerhans cell histiocytosis', 'histiocytosis X, acute disseminated', 'multifocal multisystem Langerhans cell histiocytosis', 'letterer-Siwe disease', 'acute disseminated Langerhans cell histiocytosis', 'L-S disease']",,246400,99870,C0023381,,C3160,,,,,10024265,
mondo:0009520,3-hydroxy-3-methylglutaric aciduria,"['HMG CoA lyase deficiency', '3-OH 3-Methyl glutaric aciduria', 'Hmgcl deficiency', 'HMG-CoA lyase deficiency', 'hydroxymethylglutaryl-CoA lyase deficiency', 'HMGCLD', '3-hydroxy-3-methylglutaryl-CoA lyase deficiency', 'Hydroxymethylglutaric aciduria', 'HMG-Coa lyase deficiency', 'defect in leucine metabolism', 'deficiency of hydroxymethylglutaryl-CoA lyase', 'HL deficiency']",,246450,20,C1533587,"['-0.1841', '0.1749', '-0.565', '0.02065', '-0.1362', '-0.11694', '-0.0992', '0.6733', '0.08984', '0.3584', '-0.3994', '-0.2489', '0.004204', '-0.1428', '-0.3599', '0.02087', '-0.273', '-0.3167', '-0.6704', '-0.76', '0.1815', '-0.3733', '0.62', '-0.21', '-0.397', '-0.478', '-0.228', '0.2322', '-0.4553', '-0.307', '0.544', '0.1133', '0.8145', '0.06152', '-0.589', '0.6084', '-0.668', '0.01106', '-0.3745', '0.1635', '-0.1556', '0.08276', '0.2338', '0.04044', '0.04013', '-0.1251', '0.018', '-0.1763', '-0.0968', '0.401', '-0.227', '-0.07043', '-0.4885', '-0.3403', '0.5044', '0.04602', '0.848', '-0.587', '0.001415', '0.1642', '-0.1056', '0.584', '0.572', '-0.3118', '-0.1299', '0.0589', '0.2727', '0.3123', '-0.6255', '0.4812', '-0.0928', '0.6665', '-0.6577', '-0.03546', '-0.2861', '0.266', '0.1874', '-0.2834', '-0.3357', '-0.1808', '0.6504', '-0.4968', '-0.1763', '0.021', '0.5386', '0.2284', '-0.1589', '0.101', '0.6025', '-0.1165', '0.4685', '-0.004498', '-0.32', '0.2346', '0.1492', '0.846', '0.4685', '-0.1871', '-0.2267', '0.4602']",C84523,,C538324,,,,
mondo:0009521,"leukemia, acute myelocytic, with polyposis coli and colon cancer","['leukemia, acute myelocytic, with polyposis coli and colon cancer']",,246470,,C1855505,,,,C565441,,,,
mondo:0009522,Leukomelanoderma-infantilism-intellectual disability-hypodontia-hypotrichosis syndrome,"['ectodermal dysplasia, Berlin type', 'LEUKOMELANODERMA, infantilism, mental retardation, hypodontia, hypotrichosis', 'Berlin syndrome', 'LEUKOMELANODERMA, infantilism, intellectual disability, hypodontia, hypotrichosis']",,246500,1816,C1855504,,,,C565440,,,,
mondo:0009523,Lichtenstein syndrome,"['neutropenia immunoglobulin deficiency peculiar facies and bony anomalies', 'Lichtenstein syndrome']",,246550,2390,C1855502,,,,C535894,,,,
mondo:0009524,intellectual disability-spasticity-ectrodactyly syndrome,"['limb defects, distal transverse, with mental retardation and spasticity', 'mental retardation, spasticity and transverse limb defects', 'mental retardation spasticity ectrodactyly', 'ectrodactyly, spastic paraplegia and mental retardation', 'ectrodactyly, spastic paraplegia and intellectual disability', 'intellectual disability, spasticity and transverse limb defects', 'intellectual disability spasticity ectrodactyly', 'limb defects, distal transverse, with intellectual disability and spasticity', 'Jancar syndrome']",,246555,1891,C0796001,,,,C537446,,,,
mondo:0009525,split hand-foot malformation 3,"['chromosome 10Q24 Duplication syndrome', 'split hand-foot malformation type 3', 'Shsf3', 'distal limb deficiencies with micrognathia', 'split-hand/foot malformation 3, gene duplication syndrome', 'chromosome 10q24 duplication syndrome', 'SHFM3', 'limb deficiencies distal with micrognathia', 'split-hand/foot malformation 3', 'Buttiens Fryns syndrome', 'distal limb deficiencies-micrognathia syndrome', 'limb deficiencies, distal, with micrognathia', '10q24 microduplication syndrome', 'Buttiens-Fryns syndrome', 'split-hand/foot malformation type 3']",0090025,246560,1307,,"['-0.1512', '-0.2712', '0.1652', '-0.03394', '0.1794', '0.081', '-0.05093', '0.949', '-0.00882', '-0.804', '0.1076', '-0.718', '-0.226', '0.385', '-0.00917', '-0.4404', '-0.10095', '-0.4985', '-0.3582', '-0.334', '0.03156', '-0.07684', '0.2191', '-0.07684', '0.6226', '-0.1001', '0.05438', '-0.076', '0.573', '-0.603', '-0.0361', '-0.2328', '-0.2352', '0.4038', '0.2306', '-0.6064', '-0.2124', '-0.835', '-0.7974', '-0.4758', '-0.1782', '-0.5127', '0.05026', '-0.582', '-0.644', '0.12396', '-0.353', '-0.001728', '-0.4163', '-0.235', '-0.4526', '-0.5366', '0.12067', '-0.02794', '-0.3748', '-0.924', '-0.01424', '-0.695', '-0.5713', '0.5835', '-0.3047', '-0.5625', '0.05054', '0.4875', '-0.8965', '0.3113', '-0.4448', '0.4175', '-0.2076', '0.1842', '-0.0871', '-0.05713', '0.2439', '-0.3638', '0.4304', '0.4165', '-0.1512', '-0.0513', '-0.0553', '0.06445', '-0.324', '0.4788', '0.9424', '0.76', '0.465', '-0.2206', '-0.009674', '0.2329', '0.3315', '0.2786', '0.3572', '0.709', '0.10895', '0.1825', '0.8945', '-0.2479', '-0.4976', '-0.7705', '0.1927', '0.2996']",C75121,,C565437,,,,
mondo:0009526,"fibular aplasia, tibial campomelia, and oligosyndactyly syndrome","['limb deficiency-heart malformation syndrome', 'fibular aplasia-tibial campomelia-oligosyndactyly syndrome', 'fibular aplasia, tibial campomelia, and oligosyndactyly syndrome', 'FATCO syndrome', 'terminal transverse defects of the limbs associated with congenital heart malformations']",,246570,480773,CN776928,,,,C565436,,,,
mondo:0009527,"lipase deficiency, combined","['LPL and HL deficiency', 'lipase deficiency, combined', 'combined lipase deficiency', 'LPL and HTGL deficiency', 'lipoprotein lipase deficiency with hepatic triglyceride lipase deficiency', 'lipase deficiency combined']",0111422,246650,535453,C1855498,,C126558,,C535904,,,,
mondo:0009528,chylomicron retention disease,"['lipid Transport defect of intestine', 'CRD', 'chylomicron retention disease', 'CMRD', 'Anderson disease', 'hypobetalipoproteinemia with accumulation of apolipoprotein B-like Protein in intestinal cells', 'hypobetalipoproteinemia with accumulation of apolipoprotein B-like protein in intestinal cells']",0060357,246700,71,C0795956,"['-0.3752', '-0.02937', '0.2544', '0.205', '0.3386', '-0.2179', '-0.434', '0.4114', '0.09296', '0.137', '-0.6978', '-0.4846', '0.1137', '0.3845', '-0.8335', '-0.5254', '0.05774', '0.3142', '-0.4502', '-0.5576', '-0.00824', '-0.949', '-0.1611', '-0.0167', '-0.3142', '0.08124', '-0.3215', '0.0204', '0.1888', '-0.3928', '0.7754', '-0.08923', '0.4048', '-0.6274', '-0.6274', '-0.0655', '0.1142', '-0.4067', '0.01061', '-0.04343', '-0.3792', '-0.3918', '0.4575', '0.1427', '0.1453', '-0.3564', '0.4028', '0.136', '-0.3115', '-0.1565', '0.1387', '0.4307', '0.533', '-0.539', '0.02489', '-0.4028', '0.3325', '0.2515', '-0.1266', '-0.05203', '0.05527', '0.0242', '0.1963', '-0.506', '-0.3306', '0.3435', '0.1332', '0.08575', '0.1315', '0.1475', '0.1708', '-0.2673', '0.1862', '-0.2174', '0.3484', '0.3064', '0.2864', '-0.01787', '0.3643', '0.3032', '0.1523', '-0.545', '-0.1285', '0.4495', '0.1584', '0.3281', '0.4312', '-0.03677', '0.812', '0.1512', '0.303', '0.128', '-0.5537', '0.3896', '0.366', '0.81', '-0.1477', '-0.2164', '0.6763', '-0.082']",,,C535460,,,,
mondo:0009529,pyruvate dehydrogenase E3 deficiency,"['DLDD', 'E3-deficient maple syrup urine disease', 'E3 deficiency', 'lipoamide dehydrogenase deficiency, lactic acidosis due to', 'dihydrolipoamide dehydrogenase deficiency', 'DLD deficiency', 'Dld deficiency', 'maple syrup urine disease, type III', 'maple syrup urine disease, type 3']",,246900,2394,CN043137,"['-0.5527', '0.03134', '-0.354', '0.1665', '0.2922', '-0.555', '-0.7197', '0.6934', '0.01636', '-0.11835', '-0.2438', '-0.258', '-0.0672', '-0.1671', '0.3264', '-0.1691', '0.3586', '-0.4973', '0.3599', '-0.4597', '0.2046', '-0.2399', '1.206', '-0.3914', '0.179', '0.05728', '-0.001593', '0.01563', '-0.308', '-0.1848', '0.409', '-0.05838', '0.3901', '0.2352', '-0.3982', '-0.4768', '-0.68', '0.0351', '-0.3203', '0.4084', '0.1813', '-0.1838', '0.2084', '0.4226', '-0.1149', '-0.2522', '-0.02267', '0.10187', '0.3003', '0.2598', '-0.3499', '-0.2566', '-0.09406', '0.1582', '0.234', '0.1556', '0.586', '-0.1334', '-0.3606', '0.684', '0.0683', '0.338', '0.923', '-0.06793', '-0.601', '-0.3167', '0.07007', '0.1383', '-0.363', '0.5444', '-0.1348', '0.1382', '0.03754', '0.4648', '0.343', '0.3574', '0.2251', '0.0893', '-0.3813', '0.5596', '0.547', '-0.4377', '-0.1492', '-0.3733', '0.09625', '0.3064', '0.394', '0.3162', '0.915', '-0.0583', '0.253', '0.369', '0.249', '-0.105', '0.688', '1.025', '-0.1576', '-0.3467', '0.4426', '-0.0806']",,,,,,,
mondo:0009530,lipoid proteinosis,"['lipoproteinosis', 'hyalinosis cutis Et mucosae', 'lipoid proteinosis', 'hyalinosis cutis et mucosae', 'Urbach Wiethe disease', 'lipid proteinosis', 'lipoid proteinosis of Urbach and Wiethe', 'Urbach-Wiethe disease']",14498,247100,530,C0023795,"['0.05023', '0.1611', '-0.8877', '-0.2477', '0.0768', '-0.5845', '0.2903', '0.6406', '-0.5454', '0.003899', '-0.02818', '-0.507', '-0.6274', '0.0674', '0.3645', '0.456', '-0.04218', '-0.5015', '-0.2896', '-0.4324', '-0.55', '-0.4329', '0.3994', '-0.04294', '-0.1326', '0.05112', '-0.5024', '0.329', '-0.4312', '-0.6143', '0.551', '-0.4636', '-0.2756', '-0.0621', '0.14', '-0.2524', '-0.58', '-0.2524', '0.00734', '-0.2688', '0.2954', '-0.3665', '0.1555', '0.03802', '0.2264', '0.643', '-0.0174', '-0.2717', '-0.06274', '0.271', '-0.3293', '0.461', '0.508', '0.06506', '-0.099', '0.4219', '0.1415', '0.1658', '0.1578', '-0.2228', '0.074', '0.3105', '-0.7363', '-0.1287', '-0.2084', '-0.3396', '0.7314', '-0.09076', '-0.4106', '1.002', '-0.3247', '-0.1995', '-0.229', '0.5283', '0.10297', '0.03784', '0.525', '-0.288', '0.2783', '-0.2499', '-0.1514', '-0.4946', '0.1208', '0.0466', '0.1814', '0.03128', '-0.1617', '-0.0245', '0.4075', '0.03021', '-0.1769', '0.1461', '0.01427', '0.4978', '0.7485', '-0.348', '0.05164', '-0.144', '0.2252', '-0.09534']",C84829,,D008065,272.8,,,
mondo:0009532,Miller-Dieker lissencephaly syndrome,"['Miller-Dieker lissencephaly syndrome', 'telomeric deletion 17p', 'Miller-Dieker syndrome', 'MDLS', 'chromosome 17P13.3 deletion syndrome', 'Miller-Dieker syndrome chromosome region', 'monosomy 17p13.3', 'lissencephaly due to 17p13.3 deletion']",0060469,247200,531,C0265219,"['0.3335', '0.4229', '0.3108', '-0.6465', '0.01752', '-0.6006', '0.2537', '0.391', '-1.1045', '-0.575', '-0.10815', '-0.382', '-0.084', '-0.3408', '0.501', '0.2169', '-0.2452', '-0.2208', '-0.307', '-0.274', '0.02214', '0.3677', '0.5537', '-0.0579', '0.3015', '-0.2979', '-0.387', '-0.4646', '0.2411', '-0.03078', '0.5356', '0.1733', '0.05032', '0.2314', '0.05353', '0.1836', '0.2047', '0.03952', '-0.3323', '-0.3596', '0.11035', '-0.3', '-0.4067', '-0.1648', '-0.3755', '-0.2085', '-0.3765', '-0.1816', '0.05783', '0.02423', '-0.392', '-0.3027', '-0.1357', '-0.1504', '0.00768', '0.2496', '0.11145', '0.2073', '0.35', '0.1614', '-0.04614', '0.3752', '-0.04868', '-0.0888', '0.201', '0.09155', '-0.2815', '-0.2452', '-0.975', '0.5386', '-0.1675', '0.3467', '-0.3987', '0.11115', '-0.4607', '0.4631', '0.3408', '-0.2986', '-0.4497', '-0.205', '0.2208', '0.0966', '-0.2377', '0.4812', '-0.2502', '0.2094', '-0.1565', '0.599', '0.2874', '0.275', '-0.4573', '0.32', '0.1285', '0.1175', '0.4587', '0.0543', '0.1755', '-0.4417', '0.2175', '0.391']",C124852,,,758.33,,10068361,
mondo:0009533,Dahlberg-Borer-Newcomer syndrome,"['lymphedema-hypoparathyroidism syndrome', 'Dahlberg syndrome', 'hypoparathyroidism lymphedema syndrome', 'Dahlberg Borer Newcomer syndrome', 'lymphedema hypoparathyroidism syndrome', 'hypoparathyroidism-lymphedema syndrome']",,247410,1563,C1855477,,,,C535769,,,,
mondo:0009534,chronic mucocutaneous candidiasis due to inhibition of lymphoblastic transformation,"['lymphoblastic transformation, inhibition of']",,247430,,,,,,C565433,,,,
mondo:0009536,chronic mucocutaneous candidiasis due to intrinsic defect in lymphoblastic transformation,"['lymphoblastic transformation, intrinsic defect type 1N', 'lymphoblastic transformation, intrinsic defect IN']",,247450,,C1855474,,,,C565431,,,,
mondo:0009537,lymphoid interstitial pneumonia,"['diffuse hyperplasia of bronchus-associated lymphoid tissue', 'lymphocytic interstitial pneumonia', 'lymphocytic interst. pneumonitis', 'LIP', 'lymphocytic interstitial pneumonitis', 'lymphoid interstitial pneumonia']",0050159,247610,79128,C0264511,,C27558,,C562489,516.8,J84.2,10062997,
mondo:0009538,"lymphoid system deterioration, progressive","['lymphoid system deterioration, progressive']",,247630,,C1855473,,,,C565430,,,,
mondo:0009539,"lymphoblastic leukemia, acute, with lymphomatous features","['lall', 'lymphoblastic leukemia, acute, with lymphomatous features', 'leukemia, acute lymphoblastic', 'lymphomatous All']",,247640,,C1855472,,,,C565429,,,,
mondo:0009540,chronic mucocutaneous candidiasis due to lymphokine deficiency,['lymphokine deficiency'],,247650,,C1855471,,,,C565428,,,,
mondo:0009541,"lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis","['lymphopenic hypergammaglobulinemia, antibody deficiency, autoimmune hemolytic anemia, and glomerulonephritis']",,247800,,C1855470,,,,C565427,,,,
mondo:0009542,lysine malabsorption syndrome,['lysine malabsorption syndrome'],,247950,,C0796023,,,,C563080,,,,
mondo:0009543,prominent glabella-microcephaly-hypogenitalism syndrome,"['MacDermot-Winter syndrome', 'Mac Dermot Winter syndrome', 'prominent glabella microcephaly hypogenitalism']",,247990,2083,C0796024,,,,C537714,,,,
mondo:0009544,"macrocephaly/megalencephaly syndrome, autosomal recessive","['MGCPH', 'Fryns Dereymaeker Haegeman syndrome', 'macrocephaly/megalencephaly syndrome, autosomal recessive', 'intellectual disability, macrocephaly, short stature and craniofacial dysmorphism', 'mental retardation, macrocephaly, short stature and craniofacial dysmorphism']",,248000,,C3806412,"['-0.0175', '0.01665', '0.009514', '-0.00806', '0.0132', '-0.03014', '-0.00944', '0.02255', '-0.01904', '-0.01651', '-0.01598', '-0.01006', '0.002855', '0.0006676', '-0.001588', '-0.0164', '0.003496', '-0.002241', '-0.01997', '-0.0377', '-0.01569', '-0.01839', '0.01311', '-0.013084', '0.002485', '0.00932', '-0.009056', '-0.0124', '0.010895', '-0.01894', '0.02002', '-0.00918', '0.02298', '0.01959', '-0.00898', '-0.01622', '-0.01346', '-0.006214', '-0.004852', '-0.02394', '0.006927', '-0.01447', '0.002378', '0.002508', '-0.004513', '-0.0247', '-0.01813', '0.010765', '0.004993', '0.01519', '-0.002544', '-0.01013', '0.0079', '-0.001037', '-0.003588', '-0.01392', '0.02367', '-0.006504', '-0.0366', '0.00585', '0.02155', '0.011215', '0.010445', '0.003191', '-0.002258', '0.009056', '0.03336', '0.02917', '-0.013054', '0.03123', '-0.01557', '0.00926', '-0.0002319', '-0.005074', '0.006577', '0.01743', '0.00843', '0.004307', '-0.015175', '-0.00894', '0.004715', '0.00598', '-0.007652', '0.01566', '0.001639', '-0.003134', '0.00975', '0.0207', '0.02061', '0.02148', '0.007446', '0.02252', '-0.0005617', '-0.002243', '0.0435', '0.0146', '0.02936', '-0.04486', '-0.00962', '0.014114']",,,C537453,,,,
mondo:0009545,"macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance","['McAlister coe Whyte syndrome', 'Macroepiphyseal dysplasia, McAlister coe type', 'macroepiphyseal dysplasia with osteoporosis, wrinkled skin, and aged appearance']",,248010,,C2931597,,,,C537721,,,,
mondo:0009546,macrosomia adiposa congenita,['macrosomia adiposa congenita'],,248100,,C1855468,,,,C565425,,,,
mondo:0009547,macrosomia-microphthalmia-cleft palate syndrome,"['macrosomia microphthalmia cleft palate', 'macrosomia with lethal microphthalmia', 'Teebi Al-Saleh Hassoon syndrome', 'Teebi-Al Saleh-Hassoon syndrome', 'macrosomia with microphthalmia, lethal']",,248110,2432,C1855467,,,,C537830,,,,
mondo:0009548,renal hypomagnesemia 5 with ocular involvement,"['FHHNC with severe ocular involvement', 'FHHNCOI', 'familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis with severe ocular involvement', 'hypomagnesemia, renal, with ocular involvement', 'familial hypomagnesemia with hypercalciuria, nephrocalcinosis and severe ocular involvement', 'idiopathic hypercalciuria with bilateral macular colobomata', 'hypercalciuria-bilateral macular coloboma syndrome', 'bilateral macular coloboma with hypercalciuria', 'hypomagnesemia 5, renal, with ocular involvement', 'HOMG5', 'Meier-Blumberg-Imahorn syndrome', 'macular coloboma, bilateral, with hypercalciuria', 'hypomagnesemia, familial, with hypercalciuria, nephrocalcinosis, and severe ocular involvement', 'Meier Blumberg Imahorn syndrome']",0060881,248190,2196,,"['-0.5', '-0.2351', '-0.153', '-0.383', '-0.3152', '-0.2769', '0.02324', '0.975', '-0.615', '-0.2983', '-0.5527', '-0.3257', '-0.88', '0.2151', '-0.3467', '-0.511', '0.4153', '0.02385', '0.4958', '-0.6265', '-0.135', '-0.3936', '-0.399', '-0.03099', '0.1725', '0.1035', '-0.1731', '-0.0893', '-0.1788', '0.01917', '0.278', '0.1521', '0.4656', '0.11005', '0.3157', '0.03934', '-0.294', '-0.3809', '-0.3042', '0.07904', '0.3303', '-0.01793', '0.642', '-0.2028', '-0.05057', '0.301', '-0.1708', '-0.123', '-0.329', '0.553', '0.1791', '0.8394', '0.434', '-0.5596', '-0.2302', '-0.3513', '0.1108', '-0.4531', '-0.10675', '0.1943', '0.9463', '-0.2751', '0.004116', '-0.1595', '-0.01843', '-0.2617', '0.7505', '0.6357', '-0.2208', '-0.1693', '-0.2998', '0.01134', '0.0974', '0.08514', '0.518', '0.01743', '0.1906', '0.015144', '0.3076', '0.1766', '0.4692', '-0.0357', '0.251', '0.2534', '-0.0737', '-0.0419', '0.02707', '-0.2664', '0.3843', '0.0995', '0.2124', '0.3079', '-0.04004', '0.3264', '0.9883', '-0.0448', '0.6973', '-0.4836', '-0.4253', '0.5503']",,,C536148,,,,
mondo:0009549,severe early-childhood-onset retinal dystrophy,"['SECORD', 'Stargardt disease type 1', 'Stargardt disease 1', 'Stgd', 'macular dystrophy with flecks, type 1', 'EOSRD', 'retinal dystrophy, early-onset severe', 'early-onset severe retinal dystrophy', 'macular Degeneration, juvenile', 'STGD1', 'fundus flavimaculatus']",,248200,364055,,"['-0.3315', '-0.4744', '-0.5396', '0.543', '0.672', '-0.691', '-0.12317', '0.4143', '-0.502', '-0.663', '-0.022', '0.1098', '-0.02301', '0.3225', '0.0128', '-0.833', '0.351', '-0.1185', '-0.1572', '-0.8765', '-0.2834', '-0.2869', '-0.11206', '0.4834', '0.3777', '-0.3413', '-0.4827', '0.334', '-0.4304', '0.846', '0.478', '0.3826', '0.04898', '0.31', '0.296', '-0.1044', '-0.2313', '-0.1807', '-0.09247', '-0.3862', '0.641', '-0.551', '0.465', '-0.1943', '0.1376', '0.08575', '-0.1039', '-0.556', '0.517', '0.2192', '0.3513', '0.04733', '0.06256', '-0.6587', '0.615', '0.01105', '0.7485', '0.3113', '-0.1106', '0.02638', '0.4407', '0.7334', '0.693', '0.3904', '-0.01768', '-0.05417', '0.2605', '0.4758', '-0.10187', '0.2067', '0.01582', '-0.3545', '-0.0981', '-0.2045', '0.951', '-0.584', '0.1964', '-0.4578', '-0.3313', '0.01648', '0.5415', '-0.04483', '-0.2932', '0.713', '-0.422', '-0.3984', '0.01915', '0.401', '0.806', '0.2091', '0.324', '0.6997', '-0.1478', '0.4788', '0.0227', '-0.047', '0.4243', '-0.614', '-0.1636', '0.08636']",,,,,H35.5,,
mondo:0009550,renal hypomagnesemia 3,"['CLDN16 primary hypomagnesemia', 'hypercalciuria, childhood, self-limiting', 'hypomagnesemia, isolated renal', 'renal hypomagnesemia type 3', 'primary hypomagnesemia due to defect in renal tubular transport of magnesium', 'hypomagnesemia 3, renal', 'primary hypomagnesemia caused by mutation in CLDN16', 'hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis', 'familial primary hypomagnesemia with hypercalciuria and nephrocalcinosis without severe ocular involvement', 'CLDN16 familial primary hypomagnesemia', 'magnesium, defect in renal tubular transport of', 'FHHNC without severe ocular involvement', 'hypomagnesemia, familial, with hypercalciuria and nephrocalcinosis hypercalciuria, childhood, self-limiting, included', 'isolated renal hypomagnesemia', 'hypomagnesemia, primary, due to defect in renal tubular Transport of magnesium', 'hypomagnesemia, primary, due to defect in renal tubular Transport Of magnesium', 'HOMG3']",0060880,248250,31043,,"['-0.0901', '-0.258', '-0.09766', '-0.4944', '0.04135', '-0.527', '-0.2113', '0.927', '-0.6274', '-0.283', '0.1093', '-0.2693', '-1.003', '0.3083', '-0.4277', '-0.06012', '0.2727', '-0.3772', '0.1575', '-0.446', '0.03992', '-0.3918', '-0.07404', '0.2352', '0.4622', '0.556', '-0.1489', '0.01872', '-0.1589', '-0.01817', '-0.3079', '0.00722', '0.3147', '-0.03848', '-0.2074', '-0.4248', '-0.397', '0.1698', '-0.588', '0.312', '0.2556', '-0.2664', '0.8574', '-0.526', '-0.4038', '0.1464', '-0.512', '-0.4617', '-0.3845', '0.511', '-0.1869', '0.189', '0.6904', '-0.4153', '-0.3008', '-0.4658', '0.503', '-0.446', '-0.4155', '0.2004', '0.6406', '0.2333', '-0.0854', '-0.0694', '0.169', '-0.5845', '0.432', '0.549', '-0.1517', '-0.3708', '-0.0764', '0.04352', '0.516', '0.11017', '0.2175', '0.2922', '0.382', '0.6055', '0.044', '0.502', '0.1826', '0.4573', '0.4426', '0.3276', '0.2249', '-0.01762', '0.3525', '-0.435', '0.3406', '0.4238', '0.2698', '0.2179', '0.02284', '0.04797', '1.137', '0.5166', '0.555', '-0.678', '-0.4001', '0.4404']",,,C537153,,,,
mondo:0009551,"magnesium, elevated red cell","['magnesium, elevated red cell']",,248260,,,,,,,,,,
mondo:0009552,mal de Meleda,"['MDM', 'MAL DE Meleda', 'keratosis palmoplantaris transgradiens of Siemens', 'keratosis palmoplantaris transgrediens of Siemens', 'transgrediens palmoplantar keratoderma of Siemens', 'Meleda disease', 'mal de Meleda']",0060862,248300,87503,C0025221,"['-0.065', '0.4478', '-0.02954', '-0.1927', '0.0348', '-0.9375', '0.1323', '-0.1285', '-0.0892', '0.02963', '-0.2544', '0.1992', '-0.522', '-0.013916', '-0.06207', '0.044', '0.316', '-0.8765', '0.3704', '-0.71', '-0.01171', '-0.0645', '0.5015', '-0.2384', '0.0199', '0.3628', '-0.2922', '0.1809', '-0.3516', '0.0793', '0.1547', '-0.2319', '-0.0971', '0.1808', '0.4094', '-0.11127', '0.1283', '0.2583', '-0.02367', '-0.0981', '-0.3782', '-0.558', '-0.0726', '-0.08167', '0.2747', '0.05103', '-0.4048', '0.585', '0.1747', '0.137', '-0.2021', '0.01566', '0.1787', '0.005905', '-0.1384', '-0.1562', '0.738', '-0.04163', '-0.5273', '0.156', '-0.0633', '-0.0646', '-0.2944', '-0.006325', '0.11395', '0.2056', '0.1757', '0.5347', '0.225', '0.5894', '-0.3442', '0.02992', '0.449', '0.05762', '-0.1396', '0.1913', '-0.04306', '-0.1367', '-0.03494', '-0.3286', '-0.05383', '-0.04825', '0.0605', '-0.05212', '-0.013985', '-0.2312', '-0.215', '0.7363', '0.516', '0.2886', '0.2417', '0.2472', '0.2876', '0.1864', '0.142', '0.0921', '0.5835', '-0.723', '0.126', '0.05994']",,,,757.39,,,
mondo:0009554,3MC syndrome 3,"['3MC syndrome type 3', '3MC syndrome 3', 'COLEC10 3MC syndrome', '3Mc syndrome type 3', 'Malpuech Facial clefting syndrome, formerly', 'facial clefting syndrome, Gypsy type', '3MC syndrome caused by mutation in COLEC10', '3MC3', 'Malpuech Facial clefting syndrome']",0060577,248340,2453,C0796032,,,,C535704,,,,
mondo:0009555,malocclusion and short stature,['malocclusion and short stature'],,248350,,C1855453,,,,C565421,,,,
mondo:0009556,malonic aciduria,"['malonic acidemia', 'malonyl-CoA decarboxylase deficiency', 'Malonicaciduria', 'MCD deficiency']",,248360,943,C0342793,"['-0.0802', '0.3157', '-0.3147', '-0.06052', '0.0873', '-0.2103', '-0.2041', '0.4736', '-0.02733', '-0.007965', '-0.2196', '-0.2352', '0.12', '-0.1361', '-0.0867', '0.0819', '0.11163', '0.01582', '-0.3743', '-0.782', '0.06537', '-0.443', '0.03903', '0.02252', '0.02145', '-0.1659', '-0.2161', '-0.10364', '0.1449', '-0.5327', '0.1469', '0.1757', '-0.02318', '0.4998', '-0.1998', '-0.10767', '-0.07886', '-0.2952', '-0.0711', '-0.01259', '0.1766', '-0.425', '0.3909', '-0.0474', '-0.03464', '-0.3416', '8.41e-05', '0.215', '-0.2054', '0.09216', '-0.2766', '0.06635', '0.07043', '0.169', '-0.0227', '-0.245', '0.2725', '-0.2688', '-0.07294', '0.3105', '0.4275', '0.1984', '0.706', '-0.3472', '-0.03873', '0.05844', '0.2305', '0.2065', '-0.4626', '0.2155', '-0.05948', '-0.04355', '-0.1763', '0.3108', '0.2206', '0.3728', '-0.04208', '-0.309', '-0.0938', '0.1448', '0.8164', '-0.1495', '-0.0884', '0.333', '0.3777', '0.54', '0.05334', '0.03558', '0.655', '0.196', '0.4644', '0.1149', '-0.364', '0.07263', '0.2742', '0.5757', '0.1982', '-0.3716', '0.02576', '-0.3296']",,,C535702,,,,
mondo:0009557,mandibuloacral dysplasia with type A lipodystrophy,"['mandibuloacral dysplasia', 'MADA', 'lipodystrophy, type A, associated with Mandibuloacral dysplasia', 'Mandibuloacral dysplasia with type a lipodystrophy, atypical', 'mandibuloacral dysplasia with type A lipodystrophy', 'MANDIBULOACRAL dysplasia with type A lipodystrophy', 'craniomandibular Dermatodysostosis']",0081128,248370,90153,CN236772,"['-0.3057', '0.2169', '0.158', '-0.3362', '0.435', '-0.2788', '-0.02774', '0.2896', '-0.34', '-0.1838', '-0.1218', '0.1247', '-0.1209', '-0.1881', '-0.2129', '0.3035', '0.5176', '-0.1567', '-0.3875', '-0.461', '-0.0358', '-0.1368', '0.2058', '-0.1277', '0.1305', '0.2319', '0.04446', '-0.14', '0.01311', '-0.298', '0.3523', '-0.1059', '0.0492', '-0.06235', '0.04776', '-0.10376', '-0.02086', '-0.139', '0.02696', '-0.2517', '-0.11774', '-0.2273', '0.01448', '0.1757', '-0.0904', '-0.2328', '-0.0858', '0.2477', '0.3909', '-0.2354', '-0.011925', '-0.1428', '0.2015', '0.1696', '-0.3262', '-0.4026', '-0.02437', '0.00468', '-0.3965', '-0.02086', '0.2463', '-0.1406', '-0.3284', '-0.02275', '-0.1021', '-0.01894', '0.16', '0.2703', '-0.257', '0.1667', '-0.382', '-0.0819', '0.0924', '0.01523', '0.12354', '-0.02905', '-0.02797', '0.119', '-0.1185', '-0.2961', '0.0265', '-0.02109', '0.2725', '0.1489', '-0.1708', '-0.07263', '-0.0935', '0.3333', '0.1649', '0.1758', '-0.011475', '0.4355', '0.1926', '0.1769', '0.4482', '-0.11725', '0.4016', '-0.4485', '0.33', '0.259']",C123417,,C535705,,,,
mondo:0009558,Treacher Collins syndrome 3,"['mandibulofacial dysostosis, Treacher Collins type, autosomal recessive', 'POLR1C Treacher-Collins syndrome', 'TREACHER COLLINS syndrome 3', 'TCS3', 'Treacher Collins syndrome type 3', 'Treacher Collins syndrome 3', 'Treacher-Collins syndrome caused by mutation in POLR1C']",0080791,248390,,,,,,C535707,,,,
mondo:0009559,mandibulofacial dysostosis with mental deficiency,"['mandibulofacial dysostosis with mental deficiency', 'mandibulofacial dysostosis with intellectual disability', 'mandibulofacial dysostosis with mental retardation']",,248400,,C1855432,,,,C565420,,,,
mondo:0009560,oculotrichoanal syndrome,"['Marles-Greenberg-Persaud syndrome', 'unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies', 'MOTA', 'Manitoba Trichoanal syndrome', 'Manitoba oculotrichoanal syndrome', 'MOTA syndrome', 'Marles syndrome', 'MANITOBA oculotrichoanal syndrome']",,248450,2717,C1855425,"['-0.3396', '-0.02739', '0.2805', '-0.2314', '0.1015', '-0.01576', '0.2058', '0.1995', '-0.426', '-0.1688', '-0.1549', '-0.1249', '0.0151', '-0.2305', '-0.3345', '0.0172', '0.229', '-0.1741', '-0.11975', '-0.6304', '0.01242', '0.2166', '0.3254', '-0.0904', '0.275', '-0.01997', '-0.3018', '0.0811', '0.4692', '-0.1868', '0.2156', '0.02065', '0.26', '0.2241', '0.1443', '-0.1688', '-0.03217', '-0.158', '-0.19', '-0.35', '0.2096', '-0.0908', '0.1186', '-0.3909', '0.03537', '-0.2917', '0.01298', '0.3044', '-0.1335', '0.007412', '-0.383', '-0.0353', '-0.11487', '-0.1197', '-0.2637', '-0.1448', '-0.00821', '-0.0988', '-0.1597', '0.1781', '0.294', '0.1752', '-0.1422', '0.1809', '0.05682', '-0.1405', '0.3179', '0.2408', '-0.207', '0.2961', '-0.338', '0.1611', '-0.003567', '0.1293', '-0.239', '-0.10077', '0.1367', '-0.1942', '-0.4243', '-0.1167', '0.10815', '0.2047', '0.000954', '0.548', '-0.08386', '-0.11255', '-0.0463', '0.0756', '0.1344', '0.0303', '0.02388', '0.533', '0.3267', '0.1079', '0.5503', '-0.05234', '0.411', '-0.3777', '0.2122', '0.231']",,,C536022,759.89,,,
mondo:0009561,alpha-mannosidosis,"['lysosomal Alpha-D-mannosidase deficiency', 'mannosidosis, alpha B lysosomal', 'Alpha-mannosidase B deficiency', 'mannosidosis, ALPHA B, lysosomal', 'deficiency of alpha-mannosidase', 'lysosomal alpha-D-mannosidase deficiency', 'mannosidosis, alpha-, types I and II', 'alpha-mannosidase deficiency', 'alpha-mannosidosis', 'Alpha-D-mannosidosis', 'Alpha mannosidase B deficiency', 'MANSA']",3413,248500,61,C0024748,"['0.04407', '0.4866', '-0.0727', '-0.4456', '-0.184', '-0.1506', '0.129', '1.09', '-0.776', '-0.1261', '0.4092', '0.2356', '0.2028', '-0.0781', '-0.1243', '-0.2954', '0.553', '0.1549', '-0.996', '-0.632', '-0.37', '-0.392', '0.6294', '0.369', '0.1923', '-0.4917', '-0.09503', '0.2144', '-0.2644', '-0.01118', '0.12067', '-0.0468', '-0.504', '0.05173', '-0.334', '-0.06354', '0.02818', '-0.5215', '0.04926', '-0.1716', '0.00451', '0.11755', '0.4985', '0.2274', '0.02193', '-0.1037', '0.393', '-0.506', '-0.253', '0.2722', '-0.2527', '-0.1231', '-0.092', '-0.359', '0.2717', '-0.4646', '0.06018', '0.1748', '0.1902', '-0.227', '0.2224', '-0.02525', '-0.2993', '0.7017', '-0.1528', '0.0656', '0.2255', '0.16', '0.01685', '0.02356', '-0.4475', '-0.4255', '-0.0572', '-0.116', '-0.003437', '0.192', '0.2664', '-0.03622', '-0.558', '-0.5903', '0.1633', '-0.7393', '-0.5786', '0.753', '0.08044', '0.2585', '-0.03467', '-0.1316', '0.069', '0.627', '0.2037', '0.4502', '0.3743', '0.1102', '0.323', '0.8604', '0.1304', '-0.4424', '0.7046', '0.2']",C84548,,D008363,271.8,,,
mondo:0009562,beta-mannosidosis,"['Beta-D-mannosidosis', 'Beta-mannosidase deficiency', 'lysosomal beta-mannosidase deficiency', 'mannosidosis, beta', 'MANSB', 'mannosidosis, BETA A, lysosomal', 'lysosomal Beta-mannosidase deficiency', 'beta-mannosidase deficiency', 'beta-mannosidosis']",3633,248510,118,C4048196,"['-0.237', '0.3472', '0.1038', '-0.311', '0.0581', '-0.2277', '0.1444', '0.2041', '-0.306', '-0.07874', '-0.1338', '-0.01063', '-0.02481', '-0.06885', '0.10394', '0.0996', '0.01305', '-0.0189', '-0.3657', '-0.4714', '-0.03152', '-0.1849', '0.3625', '0.02835', '0.0639', '-0.08307', '-0.10864', '0.1576', '0.05847', '-0.0974', '0.1048', '0.11487', '0.194', '0.1981', '-0.08295', '-0.2056', '-0.1489', '-0.0839', '-0.0717', '-0.1644', '0.00787', '-0.3037', '0.2698', '0.11', '-0.1376', '-0.3438', '0.11505', '0.014206', '0.177', '0.2065', '-0.1915', '0.02182', '-0.07605', '-0.04465', '0.1501', '-0.708', '0.08', '-0.1076', '-0.02051', '0.1661', '0.000173', '-0.02617', '0.3027', '0.03262', '0.1761', '0.05838', '0.006287', '0.0741', '-0.43', '0.04608', '-0.4988', '-0.1614', '0.01216', '0.0715', '0.1208', '0.2104', '0.3376', '0.0769', '-0.1575', '-0.1976', '0.1952', '-0.2102', '-0.3296', '0.3955', '0.1365', '-0.00711', '0.2489', '0.2012', '0.334', '0.3542', '0.1538', '0.4785', '-0.1091', '-0.04965', '0.4692', '0.542', '0.2361', '-0.4268', '0.3313', '-0.06033']",C84596,,D044905,271.8,,,
mondo:0009563,maple syrup urine disease,"['branched chain ketoaciduria', 'maple syrup urine disease, Intermediate', 'maple syrup urine disease, classic', 'BCKDH deficiency', 'maple syrup urine disease, intermittent', 'branched-chain Alpha-Keto acid dehydrogenase deficiency', 'branched-chain 2-ketoacid dehydrogenase deficiency', 'MSUD', 'maple syrup urine disease, type II', 'maple syrup urine disease, type IB', 'maple syrup urine disease, type 1A', 'maple syrup urine disease, type IA', 'branched-chain ketoaciduria', 'Keto acid decarboxylase deficiency', 'Ketoacidaemia', 'dihydrolipoamide dehydrogenase deficiency', 'maple syrup urine disease, thiamine-responsive', 'maple syrup urine disease', 'maple syrup urine disease, type 2', 'BCKD deficiency', 'maple syrup urine disease, type 1B']",9269,248600,511,C0024776,"['0.03406', '0.533', '-0.2015', '0.1003', '-0.2018', '-1.01', '-0.9204', '0.4465', '0.204', '-0.158', '-0.2446', '-0.552', '0.1203', '0.261', '0.373', '0.0656', '0.01872', '-0.42', '0.1359', '-0.659', '-0.02773', '-0.725', '1.25', '-0.1812', '0.04126', '-0.2886', '-0.07416', '-0.06726', '-0.509', '-0.5522', '0.3066', '0.03128', '0.4348', '0.5522', '-0.4634', '0.574', '-0.06287', '0.4673', '-0.596', '-0.0966', '0.2377', '-0.0736', '0.4182', '-0.0735', '-0.1858', '-0.05054', '-0.125', '-0.0789', '-0.2961', '1.071', '-0.343', '-0.1072', '-0.4622', '-0.808', '0.21', '-0.735', '0.599', '0.0827', '-0.394', '0.1599', '-0.001613', '0.08923', '0.3276', '-0.0275', '-0.4746', '0.1696', '0.789', '-0.0853', '-1.078', '0.1565', '-0.4775', '-0.0618', '0.08203', '-0.1344', '0.2169', '0.702', '0.1345', '-0.00854', '-0.2612', '0.106', '0.482', '-0.3965', '-0.0967', '0.1404', '0.7046', '0.1934', '-0.1786', '-0.5454', '-0.04364', '0.272', '0.2286', '0.6006', '0.0656', '0.3188', '-0.00904', '1.06', '-0.0932', '-0.575', '0.3333', '-0.06915']",C34806,,D008375,,E71.0,10026817,
mondo:0009564,Marden-Walker syndrome,"['Marden-Walker syndrome', 'MARDEN-WALKER syndrome', 'MWKS', 'Mws', 'connective tissue disorder Marden Walker type']",,248700,2461,,"['-0.11285', '-0.2932', '0.12146', '-0.6914', '0.08215', '-0.613', '0.261', '1.456', '-0.8184', '-0.4556', '-0.2109', '-0.3887', '0.2517', '0.12244', '-0.08105', '0.6055', '0.3867', '-0.5664', '-0.2322', '-0.85', '-0.1099', '-0.1786', '0.35', '0.3525', '-0.3186', '0.04202', '-0.329', '0.1578', '0.22', '-0.3867', '0.5', '-0.1536', '1.061', '0.4648', '0.03476', '-0.1853', '0.3857', '0.0465', '-0.1005', '-0.136', '-0.527', '-0.271', '-0.173', '0.1287', '0.3137', '-0.07965', '0.257', '0.732', '-0.3303', '0.002876', '-0.5293', '-0.3108', '0.2267', '0.2045', '-0.795', '-0.0863', '-0.1511', '-0.5303', '0.0683', '0.1208', '0.1852', '0.1294', '-0.561', '0.0629', '-0.1407', '-0.0932', '-0.03622', '0.518', '-0.2595', '0.1882', '-0.3982', '0.3525', '-0.1947', '0.2089', '0.5264', '0.289', '-0.05334', '0.09436', '-0.629', '-0.04935', '0.5195', '0.2378', '0.008354', '0.851', '-0.2239', '0.3684', '-0.33', '0.4841', '0.0635', '-0.1044', '0.1725', '0.2383', '0.3037', '-0.01692', '0.1644', '-0.0849', '0.6245', '-0.381', '0.5127', '0.2947']",,,C535910,759.89,,,
mondo:0009565,microcephaly-glomerulonephritis-marfanoid habitus syndrome,"['microcephaly glomerulonephritis Marfanoid habitus', 'MARFANOID habitus with microcephaly and glomerulonephritis']",,248760,2172,C1855348,,,,C565411,,,,
mondo:0009566,marfanoid habitus-autosomal recessive intellectual disability syndrome,"['MARFANOID intellectual disability syndrome, autosomal', 'Marfanoid mental retardation syndrome autosomal', 'MARFANOID mental retardation syndrome, autosomal', 'Marfanoid intellectual disability syndrome autosomal']",,248770,2463,C1855347,,,,C565410,,,,
mondo:0009567,Marinesco-Sjogren syndrome,"['Marinesco-Sjogren syndrome', 'Marinesco-Garland syndrome', 'Garland-Moorhouse syndrome', 'Marinesco-Sjögren syndrome', 'hereditary oligophrenic cerebello-lental degeneration', 'Marinesco-Sjogren syndrome-myopathy', 'Marinesco-Sjogren-Garland syndrome', 'oligophrenic cerebellolenticular degeneration', 'MSS', 'Marinesco-Sjogren syndrome-Hypergonadotrophic hypogonadism']",0080195,248800,559,C0024814,"['-0.3533', '-0.2435', '-0.2695', '-0.133', '-0.08624', '-0.0473', '0.2642', '0.8037', '-0.764', '-0.3525', '-0.7554', '-0.1571', '-0.2742', '0.1781', '0.1884', '0.408', '0.0982', '0.2627', '-0.1294', '-0.5186', '0.2773', '-0.3784', '-0.4258', '0.0842', '0.004993', '-0.12164', '-0.09467', '-0.2925', '-0.09827', '-0.3062', '0.1979', '0.4817', '0.478', '-0.05148', '-0.4355', '0.1842', '-0.1304', '0.0432', '-0.1465', '0.05762', '0.01895', '-0.2566', '0.0006504', '1.014', '0.1288', '-0.7573', '-0.07135', '0.177', '0.1061', '-0.42', '0.7896', '0.01756', '0.2795', '-0.04507', '0.1449', '-0.0525', '0.4524', '-0.4365', '-0.5474', '0.4077', '0.271', '0.07495', '0.1405', '0.3706', '-0.4841', '0.005356', '0.432', '0.559', '0.03546', '0.1439', '-0.6626', '0.3206', '0.311', '-0.481', '0.693', '-0.3037', '0.1984', '-0.4727', '0.1442', '0.01653', '0.841', '0.1873', '-0.4329', '0.338', '-0.641', '0.186', '0.3853', '0.1991', '0.2954', '0.1035', '0.8574', '0.397', '0.02411', '-0.3035', '0.4028', '0.2515', '0.5044', '-0.2842', '-0.11426', '0.483']",,,,742.4,,,
mondo:0009568,mast syndrome,"['autosomal recessive spastic paraplegia 21', 'Mast syndrome', 'hereditary spastic paraplegia 21', 'SPG21', 'mast syndrome', 'spastic paraplegia 21, autosomal recessive', 'autosomal recessive spastic paraplegia type 21']",0060245,248900,101001,C1855346,"['0.0957', '0.1078', '-0.1418', '-0.4958', '-0.3528', '-0.4482', '-0.3271', '0.03278', '-0.578', '-0.246', '-0.3025', '-0.2961', '-0.2086', '0.07477', '0.877', '0.2496', '-0.6', '-0.4148', '0.1423', '-0.3508', '0.1437', '-0.4219', '0.205', '0.09625', '-0.03723', '0.02017', '0.03854', '0.04462', '0.00276', '-0.3137', '0.2212', '0.08466', '0.4783', '0.1672', '0.2776', '-0.1025', '-0.356', '-0.5635', '-0.3203', '-0.3318', '0.6084', '-0.4155', '-0.1987', '0.2693', '0.1603', '-0.4631', '-0.1843', '0.4133', '-0.00713', '0.2013', '0.1552', '0.4187', '-0.5825', '-0.3447', '-0.0482', '-0.3875', '0.596', '-0.3745', '-0.2233', '0.714', '-0.3274', '-0.08344', '0.3337', '0.1765', '-0.7505', '0.02187', '0.294', '0.5176', '-0.0494', '0.5513', '-0.2272', '-0.0622', '-0.274', '-0.1477', '0.811', '0.17', '-0.1115', '-0.1045', '-0.2246', '-0.5264', '0.03903', '-0.2922', '0.6763', '1.06', '0.01888', '0.0539', '0.1644', '0.2607', '0.4468', '-0.00614', '0.4915', '0.1675', '0.02374', '0.5073', '0.63', '0.394', '0.489', '0.2578', '0.221', '0.003302']",,,C565409,,,,
mondo:0009569,Hennekam-Beemer syndrome,"['Hennekam Beemer syndrome', 'cutaneous mastocytosis, conductive hearing loss and microtia', 'mastocytosis cutaneous with short stature conductive hearing loss and microtia', 'skin mastocytosis hearing loss microcephaly mild dysmorphic features and severe intellectual disability', 'skin mastocytosis hearing loss microcephaly mild dysmorphic features and severe mental retardation', 'mastocytosis-short stature-hearing loss syndrome']",,248910,2135,CN201032,,,,C536033,,Q82.2,,
mondo:0009570,McDonough syndrome,"['intellectual disability, peculiar facies, kyphoscoliosis, diastasis recti, cryptorchidism, and congenital heart defect', 'mental retardation, peculiar facies, kyphoscoliosis, diastasis recti, cryptorchidism, and congenital heart defect', 'McDonough syndrome']",,248950,2471,C0796038,,,,C538158,,,,
mondo:0009571,"Meckel syndrome, type 1","['MKS', 'Meckel syndrome', 'Meckel syndrome 1', 'Meckel-Gruber syndrome, type 1', 'Meckel syndrome, type 1', 'Gruber syndrome', 'Meckel Gruber syndrome', 'Meckel syndrome caused by mutation in MKS1', 'Meckel syndrome type1', 'Meckel-Gruber syndrome', 'MKS1', 'Dysencephalia splachnocystica', 'MKS1 Meckel syndrome', 'Dysencephalia Splanchnocystica', 'Mes']",0070115,249000,,C3714506,,,,C536133,,,,
mondo:0009572,autosomal recessive familial Mediterranean fever,"['familial Mediterranean fever, autosomal recessive', 'familial Mediterranean fever, AR', 'familial MEDITERRANEAN FEVER', 'polyserositis, recurrent', 'FMF', 'familial Mediterranean fever', 'polyserositis, familial paroxysmal']",,249100,,,,,,,,,,
mondo:0009573,megaepiphyseal dwarfism,['megaepiphyseal dwarfism'],,249230,,,,,,C536140,,,,
mondo:0009574,megalencephaly with dysmyelination,"['megalencephaly with diffuse white matter hypodensity', 'megalencephaly with dysmyelination']",,249240,,C1855309,,,,C565408,,,,
mondo:0009575,thiamine-responsive megaloblastic anemia syndrome,"['thiamine metabolism dysfunction syndrome 1 (megaloblastic anemia, diabetes mellitus and deafness type)', 'TRMA', 'thiamine metabolism dysfunction syndrome 1 (megaloblastic Anemia, diabetes mellitus, and deafness type)', 'thiamine responsive megaloblastic anemia syndrome', 'thiamine metabolism dysfunction syndrome 1', 'megaloblastic anaemia thiamine-responsive with diabetes mellitus and sensorineural deafness', 'thiamine-responsive megaloblastic anemia with diabetes mellitus and sensorineural deafness', 'thiamine-responsive anemia syndrome', 'thiamine-responsive Anemia syndrome', 'Rogers syndrome', 'megaloblastic Anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness', 'thiamine responsive megaloblastic anaemia syndrome', 'thiamine-responsive megaloblastic anemia syndrome', 'thiamine-responsive megaloblastic anaemia with diabetes mellitus and sensorineural deafness', 'THMD1', 'thiamine-responsive Anaemia syndrome', 'thiamine-responsive anaemia syndrome', 'thiamine-responsive myelodysplasia', 'megaloblastic anemia thiamine-responsive with diabetes mellitus and sensorineural deafness']",0090117,249270,49827,,"['-0.1749', '0.3308', '0.0633', '0.3354', '0.5117', '-0.013954', '0.1211', '0.456', '-0.0732', '-0.327', '0.4243', '-0.2878', '0.1365', '0.4377', '-0.81', '-0.2195', '-0.6973', '0.269', '-0.3098', '-0.3599', '-0.03308', '-0.572', '0.1929', '0.02031', '0.6787', '-0.2195', '-0.2507', '-0.0483', '0.3245', '0.252', '0.0821', '0.011375', '0.6304', '0.5327', '0.457', '-0.1251', '-0.04306', '-0.4915', '0.291', '-0.2255', '-0.649', '0.3596', '0.1515', '-0.643', '-0.529', '-0.698', '0.3806', '0.387', '-0.0884', '-0.3972', '0.3145', '0.553', '0.7803', '-0.363', '0.5903', '-0.6436', '-0.169', '0.1249', '-1.064', '-0.2866', '-0.1936', '0.10095', '-0.236', '-0.1525', '-0.1663', '0.05087', '0.0819', '0.842', '-0.5723', '0.8125', '0.64', '-0.236', '-0.6333', '-0.6514', '0.335', '0.726', '0.3774', '-0.2021', '0.04965', '-0.01256', '0.6167', '-0.2844', '-0.1225', '0.175', '0.4993', '-0.54', '-0.4602', '0.1825', '0.6772', '-0.07184', '0.678', '0.2861', '0.08435', '-0.1558', '0.4553', '0.544', '0.4246', '-0.03766', '0.1737', '-0.3665']",,,C536510,,,,
mondo:0009576,megalocornea,"['anterior megalophthalmos', 'megalocornea', 'megalocornea (disease)']",0060305,249300,,,,,,C562829,,,,0007660
mondo:0009577,megalocornea-intellectual disability syndrome,"['NeuhC$user syndrome', 'megalocornea-mental retardation syndrome', 'megalocornea intellectual disability syndrome', 'Neuhäuser syndrome', 'megalocornea-intellectual disability syndrome', 'Neuhauser syndrome', 'MMR syndrome', 'megalocornea mental retardation syndrome']",,249310,2479,C0796086,,,,C536143,,,,
mondo:0009578,neurocutaneous melanocytosis,"['melanosis, neurocutaneous', 'neurocutaneous melanosis, somatic', 'neurocutaneous melanosis', 'NCMS', 'NCM', 'neurocutaneous melanosis syndrome', 'Neuromelanosis']",,249400,2481,,"['-0.01854', '0.0266', '0.02174', '-0.02046', '0.02065', '-0.03418', '-0.002995', '0.03009', '-0.02289', '-0.02728', '-0.00395', '-0.00901', '0.007435', '-0.00438', '-0.005924', '-0.01869', '0.01617', '-0.02574', '-0.03494', '-0.04596', '-0.00589', '0.004017', '0.03754', '-0.02122', '-0.007156', '0.001514', '0.000281', '-0.01021', '0.00646', '-0.02669', '0.03943', '-0.004932', '0.0322', '0.01833', '-0.002363', '-0.002653', '-0.001952', '-0.0221', '-0.002768', '-0.02538', '0.0273', '-0.04044', '0.01025', '-0.0255', '-0.003061', '-0.03607', '0.0001686', '0.01437', '0.01717', '0.00796', '-0.00824', '-0.00976', '-0.00558', '0.01198', '-0.01231', '-0.01167', '0.0315', '-0.02026', '-0.0629', '0.01057', '0.02776', '0.00455', '0.005512', '0.011284', '-0.00224', '0.005558', '0.02785', '0.0144', '-0.04184', '0.03915', '-0.01926', '0.003729', '0.008736', '0.00411', '0.004826', '0.01184', '0.01598', '-0.00864', '-0.01637', '-0.02748', '0.005306', '0.01181', '0.004955', '0.0412', '-0.02106', '-0.004425', '0.01654', '0.02733', '0.02274', '0.01498', '0.01646', '0.02765', '-0.003477', '0.00946', '0.04575', '0.00227', '0.04626', '-0.039', '0.00947', '0.01509']",,,C537387,,,,
mondo:0009579,Frank-Ter Haar syndrome,"['FRANK-TER Haar syndrome', 'Melnick-Needles syndrome, autosomal recessive, formerly', 'Frank Ter Haar syndrome', 'Ter Haar syndrome', 'Borrone Dermatocardioskeletal syndrome', 'Borrone di Rocco Crovato syndrome', 'FTHS', 'Melnick-Needles syndrome, autosomal recessive', 'megalocornea, multiple skeletal anomalies, and developmental delay', 'Borrone dermatocardioskeletal syndrome', 'autosomal recessive Melnick-Needles syndrome (formerly)', 'Frank-Ter Haar syndrome']",0111789,249420,137834,C1859406,"['-0.1295', '0.0882', '0.4414', '-0.1534', '0.414', '-0.1155', '-0.1581', '0.6973', '-0.3596', '-0.06683', '0.07544', '-0.1458', '0.05246', '-0.5303', '-0.2573', '0.266', '0.2333', '-0.00638', '-0.1293', '-0.3489', '0.2451', '0.1143', '0.29', '-0.3513', '0.0691', '-0.2056', '-0.4731', '-0.4124', '0.669', '-0.07465', '0.2397', '-0.06757', '0.1896', '0.0468', '0.3892', '0.0696', '-0.1344', '-0.2776', '-0.139', '-0.7524', '0.2465', '-0.326', '-0.1384', '-0.1556', '0.0577', '-0.4736', '0.07495', '0.6973', '-0.466', '-0.02925', '-0.1534', '-0.0343', '-0.2563', '0.2917', '-0.4917', '-0.6357', '0.04968', '0.000747', '-0.0916', '-0.1626', '0.3606', '0.1754', '-0.3455', '-0.2212', '0.3413', '-0.3665', '0.1833', '0.4026', '-0.4421', '0.278', '-0.3584', '0.2693', '0.2001', '-0.1371', '-0.3142', '0.0912', '-0.02432', '-0.2184', '-0.5835', '-0.1001', '0.347', '-0.01133', '-0.1367', '0.7705', '-0.0441', '0.10364', '0.1217', '0.2505', '0.11743', '0.2474', '0.2527', '0.5425', '0.3032', '0.10364', '0.7705', '0.3545', '0.591', '-0.3455', '0.3862', '-0.0359']",,,C537274,,,,
mondo:0009580,"intellectual disability, autosomal recessive 1","['intellectual disability, autosomal recessive 1', 'autosomal recessive non-syndromic intellectual disability caused by mutation in PRSS12', 'PRSS12 autosomal recessive non-syndromic intellectual disability', 'MRT1', 'mental retardation, autosomal recessive 1', 'intellectual disability, autosomal recessive type 1', 'mental retardation, autosomal recessive type 1']",0081177,249500,,C1855304,,,,C565406,,,,
mondo:0009581,intellectual disability-dysmorphism-hypogonadism-diabetes mellitus syndrome,"['Belgian type mental retardation syndrome', 'intellectual disability syndrome, Belgian type', 'mental retardation syndrome, Belgian type', 'Belgian type intellectual disability syndrome']",,249599,3044,C1855303,,,,C537447,,,,
mondo:0009582,Mietens syndrome,"['Mietens-Weber syndrome', 'mental retardation syndrome, Mietens-WEBER type', 'corneal opacity, nystagmus, flexion contracture of the elbows, growth failure, and intellectual disability', 'mental retardation syndrome, Mietens Weber type', 'corneal opacity, nystagmus, flexion contracture of the elbows, growth failure, and mental retardation', 'intellectual disability syndrome, Mietens-WEBER type', 'intellectual disability, Mietens-Weber type', 'intellectual disability syndrome, Mietens Weber type']",,249600,2557,C0265249,,,,C537444,759.89,,,
mondo:0009583,"blepharophimosis - intellectual disability syndrome, Ohdo type","['mental retardation, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth', 'blepharophimosis syndrome, Ohdo type', 'Ohdo blepharophimosis syndrome', 'Ohdo-Madokoro-Sonoda syndrome', 'intellectual disability, congenital heart disease, blepharophimosis, blepharoptosis, and hypoplastic teeth', 'BMRS, Ohdo type', 'Ohdo syndrome']",,249620,2728,C0796094,,,,,525.8,,,
mondo:0009584,"intellectual disability, Buenos-Aires type","['intellectual disability, Buenos Aires type', 'intellectual disability Buenos Aires type', 'mental retardation Buenos Aires type', 'mental retardation, Buenos Aires type', 'Mutchinick syndrome', 'intellectual deficit Buenos-Aires type']",,249630,3079,C0796080,,,,C563095,,,,
mondo:0009585,encephalopathy due to beta-mercaptolactate-cysteine disulfiduria,"['Ampola syndrome', 'MCDU', '3-mercaptopyruvate sulfurtransferase deficiency', 'disulfiduria, mixed', 'mercaptolactate-cysteine disulfiduria', 'Beta-mercaptolactate cysteine disulfiduria']",,249650,1035,C0796055,"['-0.4607', '0.1614', '0.1328', '0.04086', '0.08075', '-0.2013', '-0.1869', '0.632', '-0.3215', '-0.07574', '-0.2722', '-0.1764', '0.0671', '-0.3525', '-0.05942', '0.10803', '0.338', '0.1929', '-0.4575', '-0.4019', '0.005672', '-0.198', '0.1656', '-0.257', '0.01848', '-0.2224', '0.06384', '0.04785', '0.08966', '0.04672', '0.1798', '-0.03072', '0.2239', '0.1327', '-0.3274', '-0.2336', '0.2668', '-0.3215', '0.2278', '-0.4797', '0.318', '-0.3718', '0.1006', '-0.5557', '-0.1427', '-0.10614', '0.3933', '0.2415', '-0.2369', '0.11115', '-0.3638', '-0.11414', '0.0323', '0.0895', '0.01389', '0.0744', '0.1643', '-0.1519', '-0.3328', '0.12213', '0.2937', '-0.288', '0.06903', '-0.2595', '0.11786', '-0.1348', '0.2059', '0.2817', '-0.2585', '0.1874', '-0.3633', '0.211', '-0.1659', '0.004772', '-0.06647', '0.2654', '0.4856', '-0.4055', '0.069', '0.107', '0.2327', '0.4028', '-0.1284', '0.6323', '0.2817', '0.3015', '-0.2017', '0.3413', '0.1436', '0.2274', '0.1694', '0.2048', '-0.415', '-0.0211', '0.41', '0.0867', '0.11896', '-0.4363', '0.2161', '-0.03522']",,,C563085,,,,
mondo:0009586,"mesangial sclerosis, diffuse renal, with ocular abnormalities","['mesangial sclerosis, diffuse renal, with ocular abnormalities']",,249660,,C1855282,,,,C565405,,,,
mondo:0009587,mesoaxial hexadactyly and cardiac malformation,"['Mexican Cardiomelic dysplasia', 'mesoaxial hexadactyly and cardiac malformation']",,249670,,C0796057,,,,C563087,,,,
mondo:0009588,Langer mesomelic dysplasia,"['LMD', 'mesomelic dwarfism, Langer type', 'mesomelic dwarfism of the hypoplastic ulna, fibula, and mandible type', 'mesomelic dwarfism of the hypoplastic ulna, fibula and mandible type', 'Langer type mesomelic dysplasia', 'dyschondrosteosis, homozygous', 'Langer mesomelic dysplasia', 'Langer syndrome', 'langer mesomelic dysplasia, pseudoautosomal recessive']",,249700,2632,C0432230,"['-0.4797', '-0.0003555', '0.05975', '-0.1521', '0.312', '-0.5835', '0.515', '1.723', '-0.6445', '-1.106', '0.1394', '-0.09753', '-0.12103', '-0.03174', '0.2115', '0.1908', '0.488', '-0.0885', '-0.2544', '-0.657', '-0.404', '0.09735', '1.091', '-0.1935', '0.1447', '0.642', '0.2664', '0.2198', '-0.09064', '0.0681', '0.2822', '-0.357', '-0.368', '-0.1562', '0.03108', '-0.0979', '0.084', '-0.3987', '-0.2037', '-0.09955', '-0.4277', '-0.299', '0.06195', '-0.1914', '0.194', '0.003077', '-0.4912', '0.346', '0.566', '-0.00821', '0.1112', '-0.8213', '-0.0902', '-0.04993', '-0.5933', '-0.346', '0.01811', '-0.4978', '0.0953', '0.4385', '0.10535', '0.0734', '0.06235', '-0.0922', '-0.4646', '0.2081', '0.03232', '0.526', '-0.235', '-0.3318', '-0.2172', '0.311', '0.215', '0.1173', '0.00522', '0.495', '-0.07153', '0.02176', '-0.2544', '-0.1737', '-0.1032', '0.2659', '-0.03644', '0.4778', '0.06042', '0.5615', '0.04254', '0.06323', '0.5894', '0.04016', '-0.02618', '-0.1841', '-0.4263', '-0.07947', '0.67', '-0.3154', '0.6455', '-0.9243', '0.489', '0.0743']",C126876,,C537267,756.59,,,
mondo:0009589,mesomelic dwarfism-cleft palate-camptodactyly syndrome,"['Reardon-Hall-Slaney syndrome', 'mesomelic dwarfism cleft palate camptodactyly', 'mesomelic dysplasia, Kozlowski-Reardon type', 'mesomelic limb shortening and bowing', 'mesomelic dysplasia, Reardon type']",,249710,2631,,,,,C565404,,,,
mondo:0009590,metachromatic leukodystrophy due to saposin B deficiency,"['metachromatic leukodystrophy due to sap-B deficiency', 'metachromatic leukodystrophy due to cerebroside sulfatase activator deficiency', 'metachromatic leukodystrophy due to saposin b deficiency', 'saposin B deficiency']",,249900,,C0268262,,,,C562609,,,,
mondo:0009591,"metachromatic leukodystrophy, juvenile form","['MLD, juvenile form', 'MLD', 'leukodystrophy metachromatic', 'cerebral sclerosis, diffuse, metachromatic form', 'metachromatic leukodystrophy, juvenile', 'cerebroside sulfatase deficiency', 'Mld', 'ARSA deficiency', 'cerebral sclerosis diffuse metachromatic form', 'metachromatic leukodystrophy', 'metachromatic leukodystrophy, late infantile', 'pseudoarylsulfatase A deficiency', 'metachromatic leukodystrophy, adult', 'sulfatide lipidosis', 'arylsulfatase A deficiency, juvenile form', 'arylsulfatase A deficiency', 'metachromatic leukoencephalopathy']",,250100,309263,,"['0.01613', '0.589', '0.3484', '0.4233', '-0.3228', '-0.3606', '-0.424', '0.5986', '-0.3052', '-0.0887', '0.0518', '0.01133', '-0.00923', '0.1716', '0.279', '-0.2822', '-0.4211', '-0.2688', '-0.674', '0.0797', '-0.1642', '-0.5835', '-0.3438', '0.2815', '0.598', '-0.686', '-0.7847', '-0.013794', '-0.389', '0.2437', '0.1333', '0.1792', '0.5044', '-0.1925', '0.2983', '-0.08014', '-0.8784', '-0.00873', '0.5337', '-0.2104', '0.3816', '-0.514', '-0.04025', '0.6655', '0.3484', '-0.04425', '0.3335', '-0.957', '0.571', '0.754', '0.524', '0.3984', '-0.246', '-0.4065', '0.3591', '-0.347', '0.51', '0.5366', '-0.192', '-0.5146', '-0.0753', '0.0203', '0.711', '0.4363', '-0.258', '0.2615', '0.256', '0.2712', '-0.609', '-0.1444', '-0.1514', '0.1394', '0.106', '-0.735', '0.1182', '0.1636', '0.3542', '0.9873', '-0.1354', '-0.1586', '0.2422', '-0.512', '-0.06885', '-0.05118', '0.3257', '0.166', '0.4824', '-0.12085', '0.3176', '0.718', '0.1223', '0.599', '-0.2522', '0.4172', '0.541', '0.1298', '-0.3923', '-0.6323', '0.3984', '0.409']",,,,,,,
mondo:0009592,metaphyseal acroscyphodysplasia,"['wedge-Shaped epiphyses of knees', 'metaphyseal acroscyphodysplasia', 'cupped metaphyses and cone-Shaped epiphyses of knees with brachydactyly', 'intellectual disability-short stature-wedge-shaped epiphyses of knees syndrome', 'Bellini syndrome', 'Bellini Chiumello Rimoldi syndrome', 'wedge-shaped epiphyses of knees', 'wedge-shaped epiphyses of the knees with mental retardation and short stature', 'wedge-shaped epiphyses of the knees with intellectual disability and short stature']",,250215,1240,C1855243,,,,C537350,,,,
mondo:0009593,"spondylometaphyseal dysplasia, Sedaghatian type","['spondylometaphyseal dysplasia, Sedaghatian type', 'spondylometaphyseal dysplasia Sedaghatian type', 'metaphyseal chondrodysplasia, congenital lethal', 'Sedaghatian chondrodysplasia', 'SMDS', 'lethal metaphyseal dysplasia']",0112298,250220,93317,C1855229,"['-0.7188', '0.3845', '0.1722', '-0.3066', '-0.005787', '-0.5757', '-0.0464', '0.912', '-0.2465', '-0.3145', '-0.6924', '-0.355', '0.04532', '-0.3313', '0.02342', '-0.11847', '0.2153', '0.1447', '-0.1981', '-0.429', '0.1665', '-0.0408', '0.523', '-0.4004', '-0.01208', '-0.09296', '0.02672', '0.2004', '0.1636', '-0.1175', '0.1304', '0.0857', '0.4016', '0.0848', '0.506', '0.001582', '-0.3335', '-0.4602', '-0.03625', '0.2827', '0.03812', '-0.692', '0.03992', '-0.3428', '-0.353', '0.2014', '-0.3057', '0.422', '-0.243', '-0.3425', '0.4382', '0.2556', '-0.09204', '0.5127', '-0.4822', '-0.393', '0.03534', '-0.2136', '0.1121', '0.2727', '0.1514', '0.09717', '-0.2197', '-0.3394', '-0.2277', '-0.3643', '0.1256', '0.4119', '-0.3782', '0.2632', '0.213', '0.1919', '0.1606', '-0.0945', '-0.304', '0.2595', '-0.0439', '-0.012764', '-0.504', '-0.1123', '-0.3237', '-0.01513', '-0.03986', '0.0261', '-0.1576', '-0.2893', '0.07715', '0.331', '-0.0819', '-0.1982', '0.10944', '0.001836', '0.05417', '0.2463', '0.7017', '0.09644', '0.7373', '-0.6562', '0.2424', '0.04358']",,,C535798,,,,
mondo:0009594,"metaphyseal chondrodysplasia, Kaitila type","['metaphyseal chondrodysplasia, Kaitila type']",,250230,166038,C1855217,,,,C565400,,,,
mondo:0009595,cartilage-hair hypoplasia,"['metaphyseal chondrodysplasia McKusick type', 'CHH', 'autosomal recessive metaphyseal chondrodysplasia', 'metaphyseal chondrodysplasia, Mckusick type', 'cartilage hair hypoplasia like syndrome', 'metaphyseal chondrodysplasia, McKusick type', 'McKusick type metaphyseal chondrodysplasia', 'cartilage-hair hypoplasia', 'cartilage hair hypoplasia']",14773,250250,175,C0220748,,C61245,,C535916,,,10069596,
mondo:0009596,"metaphyseal chondrodysplasia, Pena type","['metaphyseal chondrodysplasia, Pena type']",,250300,,C1855195,,,,C565399,,,,
mondo:0009597,"metaphyseal chondrodysplasia, Spahr type","['metaphyseal dysplasia, Spahr type', 'metaphyseal chondrodysplasia Spahr type', 'metaphyseal chondrodysplasia, Spahr type', 'MDST', 'Spahr type metaphyseal chondrodysplasia']",,250400,2501,C0432225,"['-0.584', '0.1153', '0.337', '-0.4194', '0.3054', '-0.2236', '-0.183', '0.5474', '-0.4866', '0.1731', '-0.1876', '0.2195', '-0.07544', '0.04794', '0.06445', '0.1667', '0.4116', '-0.09686', '-0.2095', '-0.6836', '0.01857', '0.05338', '0.4465', '-0.1636', '0.03854', '0.2148', '0.2258', '-0.0868', '0.109', '-0.10406', '0.0632', '-0.1924', '0.1531', '0.1998', '0.2676', '-0.06665', '-0.1855', '-0.353', '0.09674', '-0.1545', '0.01446', '-0.2312', '-0.02495', '0.1364', '-0.1356', '-0.2732', '-0.1514', '0.3345', '0.06683', '-0.007397', '0.06964', '0.1584', '-0.12067', '0.074', '-0.2603', '-0.6313', '-0.1396', '-0.2947', '-0.2302', '0.12274', '0.2477', '0.0642', '-0.4153', '-0.01456', '-0.1672', '-0.0235', '0.3757', '0.4697', '0.04437', '0.1412', '-0.3271', '-0.1465', '0.1213', '-0.3242', '0.06635', '0.004738', '-0.07184', '-0.0883', '-0.02592', '-0.3992', '-0.07965', '-0.0762', '0.1433', '0.2322', '-0.2068', '0.2184', '0.04187', '0.1693', '0.4778', '0.1309', '-0.0748', '0.253', '-0.0685', '0.3547', '0.2908', '0.3083', '0.507', '-0.2888', '0.187', '0.0465']",,,C537353,,,,
mondo:0009598,metaphyseal chondrodysplasia-retinitis pigmentosa syndrome,"['brachydactyly-short stature-retinitis pigmentosa syndrome', 'RPSKA', 'metaphyseal chondrodysplasia with retinitis pigmentosa', 'retinitis pigmentosa with or without skeletal anomalies']",,250410,166035,C1855188,"['-0.394', '0.10144', '0.3098', '-0.335', '0.0937', '-0.3425', '-0.03117', '0.3315', '-0.3462', '-0.2727', '-0.1854', '0.0658', '-0.0325', '-0.1317', '0.01028', '-0.307', '-0.00687', '0.0594', '-0.1384', '-0.6567', '-0.01313', '0.06354', '0.05023', '-0.04968', '0.1262', '0.1863', '-0.2744', '-0.10406', '0.2053', '-0.1382', '0.1133', '-0.10175', '0.2852', '0.1807', '0.1716', '-0.1044', '-0.003176', '-0.4417', '-0.2263', '-0.2903', '0.1539', '-0.1626', '-0.1948', '-0.1135', '-0.03836', '-0.1456', '-0.07776', '0.3145', '0.106', '-0.1909', '-0.03326', '0.1217', '-0.04825', '-0.269', '-0.125', '-0.3975', '0.03207', '-0.1503', '-0.123', '0.1714', '0.1686', '-0.04614', '-0.01778', '0.1184', '-0.2698', '-0.02861', '0.2124', '0.4385', '-0.3528', '0.12305', '-0.586', '0.0368', '0.00925', '-0.1721', '0.0385', '-0.2477', '0.074', '-0.1953', '-0.04205', '-0.1573', '0.0387', '0.04578', '-0.2189', '0.5957', '-0.1333', '0.0425', '-0.01291', '0.3425', '0.2852', '0.1624', '0.0802', '0.3706', '0.1901', '0.121', '0.442', '-0.05215', '0.538', '-0.3218', '0.2866', '0.2163']",,,C565398,,,,
mondo:0009599,metaphyseal dysostosis-intellectual disability-conductive deafness syndrome,"['metaphyseal dysostosis intellectual disability conductive deafness', 'metaphyseal dysostosis, conductive hearing loss and mental retardation', 'metaphyseal dysostosis, mental retardation, and conductive deafness', 'metaphyseal dysostosis mental retardation conductive deafness', 'metaphyseal dysostosis, intellectual disability, and conductive deafness', 'metaphyseal dysostosis, conductive hearing loss and intellectual disability']",,250420,2502,C1855175,,,,C565396,,,,
mondo:0009600,"metaphyseal dysplasia, anetoderma, and optic atrophy","['metaphyseal dysplasia, anetoderma, and optic atrophy']",,250450,,C1855174,,,,C565395,,,,
mondo:0009601,metaphyseal dysplasia without hypotrichosis,"['CHHV', 'cartilage-hair hypoplasia-like skeletal dysplasia without hypotrichosis or immunodeficiency', 'MDWH', 'metaphyseal dysplasia without hypotrichosis', 'cartilage-hair hypoplasia variant, skeletal manifestations only']",,250460,1838,C1834821,,,,C563574,,,,
mondo:0009602,"metaphyseal modeling abnormality, skin lesions, and spastic paraplegia","['Roy Maroteaux Kremp syndrome', 'metaphyseal modeling abnormality, skin lesions, and spastic paraplegia']",,250500,,C1855164,,,,C535875,,,,
mondo:0009603,3-hydroxyisobutyryl-CoA hydrolase deficiency,"['HIBCHD', '3-hydroxyisobutyryl-CoA hydrolase deficiency', 'Beta-hydroxyisobutyryl-CoA deacylase deficiency', 'methacrylic aciduria', 'valine metabolic defect', 'HIBCH deficiency', 'methacrylic acid toxicity', '3-hydroxyisobutryl-CoA hydrolase deficiency', 'beta-hydroxyisobutyryl Coa deacylase deficiency', 'neurodegeneration due to 3-hydroxyisobutyryl-CoA hydrolase deficiency']",,250620,88639,,"['-0.4312', '0.3228', '0.1418', '-0.03586', '0.7197', '-0.693', '-0.3728', '0.7876', '-0.4724', '-0.2064', '-0.3152', '-0.04572', '-0.0838', '-0.3545', '0.6865', '0.2338', '-0.02075', '-0.2722', '-0.768', '-0.4915', '0.2842', '-0.346', '0.483', '-0.3958', '0.2091', '-0.184', '-0.1007', '-0.1985', '-0.3508', '-0.2588', '0.4392', '0.1914', '0.0008264', '0.084', '0.1594', '-0.3445', '0.07764', '-0.11395', '-0.01717', '-0.05194', '0.2048', '-0.3975', '-0.1329', '0.2041', '-0.1637', '-0.2317', '0.3613', '0.2244', '-0.1302', '-0.02443', '-0.1006', '-0.2223', '-0.2686', '0.4622', '0.1129', '-0.3699', '0.3943', '-1.78e-05', '-0.6675', '0.7173', '0.1486', '0.3042', '0.465', '0.2988', '0.1194', '-0.10144', '0.01159', '0.4138', '-0.35', '0.02693', '-0.5396', '-0.2969', '0.07404', '0.02744', '0.174', '0.3389', '-0.1003', '0.4976', '-0.207', '0.1937', '0.5625', '-0.0363', '-0.04117', '0.2213', '0.0503', '-0.1019', '0.2522', '0.5312', '0.5347', '0.146', '-0.01098', '0.4668', '-0.02747', '-0.3267', '0.5605', '0.4768', '0.2477', '-0.6', '0.04266', '-0.393']",,,C562803,,,,
mondo:0009604,methemoglobin reductase deficiency,"['methemoglobin reductase deficiency', 'TPNH-methemoglobin reductase deficiency', 'NADPH-dependent methemoglobin reductase deficiency']",,250700,,C0472786,,,,C563171,,,,
mondo:0009605,methemoglobinemia type 4,"['METAG', 'methemoglobinemia due to deficiency of cytochrome B5', 'CYB5A methemoglobinemia', 'methemoglobinemia type IV, formerly', 'methemoglobinemia due to deficiency of cytochrome B5, formerly', 'methemoglobinemia type IV', 'methemoglobinemia caused by mutation in CYB5A', 'isolated 17,20-lyase deficiency, Pure', 'methemoglobinemia and ambiguous genitalia']",0112316,250790,,C2673427,,,,C567102,,,,
mondo:0009606,methemoglobinemia due to deficiency of methemoglobin reductase,"['methemoglobinemia, type 1', 'methemoglobinemia, type II', 'NADH-cytochrome B5 reductase deficiency, type 2', 'NADH-dependent methemoglobin reductase deficiency', 'methemoglobinemia, type 2', 'methemoglobinemia due to deficiency of methemoglobin reductase', 'NADH-cytochrome B5 reductase deficiency', 'NADH cytochrome B5 reductase deficiency', 'NADH-cytochrome B5 reductase deficiency, type 1', 'methemoglobinemia, congenital, autosomal recessive', 'NADH diaphorase deficiency', 'NADH methemoglobin reductase deficiency', 'methemoglobinemia, type I']",,250800,,C0268193,,,,,,,,
mondo:0009607,methionine adenosyltransferase deficiency,"['brain demyelination due to methionine adenosyltransferase deficiency', 'methionine adenosyltransferase deficiency, autosomal recessive', 'MAT I/III deficiency', 'hypermethioninemia, isolated persistent', 'methionine adenosyltransferase I/III deficiency', 'Mat I/III deficiency', 'methionine adenosyltransferase deficiency', 'hypermethioninemia, persistent, autosomal dominant, due to methionine adenosyltransferase I/III deficiency', 'MAT deficiency', 'isolated persistent hypermethioninemia']",,250850,168598,,"['-0.4607', '0.3477', '-0.11566', '0.02739', '0.1338', '-0.1387', '-0.321', '-0.1483', '0.03494', '0.02272', '-0.01889', '-0.1753', '0.1392', '-0.03763', '0.0473', '-0.0734', '0.065', '-0.1858', '-0.563', '-0.4465', '-0.09344', '-0.3083', '0.3596', '0.0085', '-0.03732', '-0.0953', '-0.02931', '-0.1111', '-0.02332', '-0.0703', '0.36', '-0.0772', '0.315', '0.155', '-0.206', '-0.141', '0.0655', '-0.4348', '0.2625', '-0.2322', '-0.002857', '-0.592', '0.1831', '0.04303', '-0.257', '-0.1985', '-0.0167', '0.0331', '0.08203', '0.2522', '0.323', '-0.03555', '-0.136', '0.2107', '-0.04288', '-0.0613', '0.447', '0.04333', '-0.3667', '0.4414', '0.2263', '-0.09265', '0.4717', '-0.2267', '-0.1606', '0.1997', '0.3389', '-0.02948', '-0.3604', '0.1842', '-0.373', '0.02893', '-0.0897', '-0.07526', '0.3054', '0.2421', '0.3281', '0.109', '0.01668', '-0.0739', '0.05807', '0.0633', '0.422', '-0.01636', '0.2411', '0.1913', '0.1945', '0.1072', '0.4558', '0.1257', '0.1562', '0.4985', '-0.1785', '-0.3125', '0.283', '0.478', '0.2083', '-0.3813', '0.2163', '0.1844']",C123435,,,,,,
mondo:0009608,methionine malabsorption syndrome,"['oasthouse urine disease', 'methionine malabsorption syndrome', 'Smith-strang disease']",,250900,,C0268622,,,,C562682,,,,
mondo:0009609,methylcobalamin deficiency type cblG,"['homocystinuria-megaloblastic Anemia due to defect in cobalamin metabolism, cblG complementation type', 'functional methionine synthase deficiency type cblG', 'homocystinuria-megaloblastic anemia, cblG complementation type', 'cblG', 'HMAG', 'homocystinuria-megaloblastic Anaemia due to defect in cobalamin metabolism, cblG complementation type', 'methionine synthase deficiency', 'homocystinuria due to defect in methylation Cbl g', 'methylmalonic aciduria and homocystinuria type cblG', 'methylcobalamin deficiency Cbl G type', 'methylcobalamin deficiency, cblG type']",0112256,250940,2170,,"['-0.2217', '0.4082', '-0.02437', '-0.0547', '-0.1238', '-0.3687', '-0.2974', '0.2644', '-0.3818', '-0.3845', '-0.1034', '-0.011925', '0.254', '0.2097', '-0.1587', '0.07245', '-0.1439', '-0.111', '-0.2603', '-0.397', '-0.2104', '-0.4556', '0.0775', '0.01541', '0.2656', '0.1126', '-0.0165', '-0.02925', '-0.1183', '-0.02832', '0.1926', '0.1869', '0.01682', '0.1301', '-0.12366', '0.369', '0.1825', '-0.2798', '-0.01791', '-0.10486', '0.10425', '-0.1683', '0.03323', '0.09735', '-0.462', '-0.3223', '0.3281', '-0.1567', '0.1423', '0.392', '0.0653', '-0.1694', '-0.1439', '-0.03613', '0.02266', '-0.2325', '0.10693', '0.3027', '-0.1344', '0.512', '0.2333', '0.1404', '0.0471', '-0.2534', '-0.01901', '-0.010284', '0.3804', '0.10345', '-0.4133', '0.0991', '-0.01361', '0.1003', '-0.3315', '-0.2054', '0.187', '0.615', '0.1071', '-0.2369', '-0.053', '0.1025', '0.5635', '-0.02638', '-0.3606', '-0.0897', '0.1865', '0.2937', '-0.06726', '0.01121', '0.8237', '0.1837', '0.02757', '0.1527', '0.1919', '-0.1617', '0.2345', '0.4668', '0.11523', '-0.2544', '0.2351', '0.006454']",,0005597,,,,,
mondo:0009610,3-methylglutaconic aciduria type 1,"['3-methylglutaconyl-CoA hydratase deficiency', '3-METHYLGLUTACONIC aciduria, type I', '3MG-CoA hydratase deficiency', '3 methylglutaconic aciduria type 1', '3-Mg-Coa-hydratase deficiency', '3 methylglutaconyl CoA hydratase deficiency', 'MGCA1', '3-methylglutaconic aciduria caused by mutation in auh', '3-Methylglutaconic aciduria, type 1', 'MGA type I', 'MGA1', 'Mga, type 1', '3-MGCA type I (3-MGCA-1)', '3MG CoA hydratase deficiency', 'AUH 3-methylglutaconic aciduria', '3-methylglutaconyl-CoA hydratase deficiency (auh defect)', '3-methylglutaconic aciduria type I', '3-methylglutaconyl-Coa hydratase deficiency', 'auh 3-methylglutaconic aciduria', '3 alpha methylglutaconic aciduria type I']",0110002,250950,67046,C0342728,"['-0.00411', '0.2041', '-0.3906', '-0.05402', '-0.1509', '-0.5474', '-0.08545', '0.602', '-0.663', '-0.2427', '-0.675', '-0.3418', '-0.0515', '-0.1456', '-0.2267', '0.1613', '0.05362', '-0.1304', '-0.4355', '-0.9995', '0.0707', '-0.473', '0.2844', '0.2817', '-0.0954', '-0.09576', '-0.05438', '0.08716', '-0.1023', '-0.381', '0.3845', '0.178', '0.5044', '-0.06143', '-0.7124', '0.3606', '-0.2196', '-0.03757', '0.05014', '0.548', '0.06464', '-0.5435', '0.1967', '0.4644', '0.0809', '-0.318', '-0.1654', '-0.2617', '-0.10803', '-0.0436', '-0.233', '-0.10675', '-0.3892', '-0.001199', '0.178', '-0.298', '0.512', '-0.1937', '-0.0008664', '0.3423', '-0.0909', '0.05972', '0.7812', '-0.2656', '-0.545', '-0.1973', '0.4202', '0.5137', '-0.4753', '0.236', '-0.6245', '-0.1842', '-0.3794', '0.1642', '0.328', '0.2695', '0.1385', '-0.3882', '0.1138', '-0.00927', '0.271', '0.0945', '-0.1395', '0.139', '0.333', '0.9307', '-0.3528', '0.515', '0.713', '0.6206', '0.3967', '0.1271', '-0.0937', '-0.0823', '0.1459', '0.7583', '-0.00848', '-0.4019', '0.6455', '-0.0572']",C98683,,C562801,,,,
mondo:0009611,3-methylglutaconic aciduria type 4,"['Not otherwise specified 3-MGA-Uria type', 'MGA4', 'MGCA4', '3-Methylglutaconic aciduria, type 4', '3 methylglutaconic aciduria type IV', '3 alpha methylglutaconic aciduria type IV', '3-methylglutaconic aciduria type IV', 'MGA type IV', '3-METHYLGLUTACONIC aciduria, type IV', 'Mga, type 4']",0110006,250951,67048,C1855126,,,,C565393,,,,
mondo:0009612,methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency,"['methylmalonyl-CoA mutase deficiency', 'methylmalonyl-Coenzyme A mutase deficiency', 'methylmalonic aciduria, mut(0) type', 'MCM deficiency', 'methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency', 'vitamin B12-unresponsive methylmalonic aciduria', 'methylmalonic aciduria, mut type', 'methylmalonic acidemia due to methylmalonyl-Coa mutase deficiency MMA due to MCM deficiency', 'vitamin B12-unresponsive methylmalonic acidemia', 'methylmalonic aciduria mut type', 'methylmalonic acidemia due to methylmalonyl-CoA mutase deficiency', 'methylmalonic aciduria, mut(-) type']",0060740,251000,27,C1855114,"['-0.1561', '0.1403', '0.02069', '0.02205', '0.05884', '-0.1322', '-0.0577', '0.1309', '-0.04285', '0.0031', '-0.06885', '0.003273', '0.0002615', '-0.0674', '-0.05887', '-0.0882', '-0.02892', '-0.03784', '-0.126', '-0.2559', '-0.004036', '-0.1123', '0.1232', '-0.02715', '0.02257', '-0.001306', '0.003807', '-0.0736', '-0.03198', '-0.08527', '0.01947', '0.0937', '0.12213', '0.1018', '0.01602', '-0.12384', '0.002272', '-0.1134', '-0.05646', '-0.1016', '0.02016', '-0.2299', '0.06104', '-0.01765', '-0.1743', '-0.0986', '0.0596', '0.07495', '0.02522', '0.0763', '-0.06665', '-0.10925', '0.011375', '0.00581', '-0.0882', '-0.007637', '0.1936', '-0.0803', '-0.1804', '0.10864', '0.1371', '0.04828', '0.1092', '-0.04587', '0.0474', '0.01877', '0.1522', '0.0513', '-0.1544', '0.1324', '-0.0827', '-0.01425', '-0.0662', '-0.0822', '0.0447', '0.1139', '0.0714', '-0.11255', '-0.04517', '0.012245', '0.0807', '-0.00859', '-0.0703', '0.0908', '0.0927', '0.05255', '0.05933', '0.129', '0.2495', '0.01808', '0.1094', '0.06934', '-0.08', '-0.04736', '0.2563', '0.2164', '0.0981', '-0.184', '-0.03017', '0.0637']",C148366,,C565390,,,,
mondo:0009613,"methylmalonic aciduria, cblA type","['vitamin B12-responsive methylmalonic acidemia type cblA', 'methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA type', 'MMA Cbl A type', 'methylmalonic acidemia, cblA type', 'methylmalonic acidemia cblA type', 'methylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cblA type', 'vitamin B12-responsive methylmalonic aciduria type cblA', 'methylmalonic aciduria cblA type', 'methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblA complementation type', 'Methylmalonic aciduria, vitamin B12-responsive, cblA type', 'methylmalonic aciduria, cblA type', 'methylmalonic aciduria, vitamin B12-responsive due to a defect in synthesis of adenosylcobalamin cb1A type']",0060742,251100,79310,C1855109,"['-0.1627', '0.3464', '-0.01717', '-0.05298', '0.1317', '-0.3538', '-0.3884', '0.02615', '-0.25', '-0.1907', '-0.2345', '-0.0148', '0.1642', '-0.2766', '-0.05792', '-0.1569', '-0.09503', '-0.2091', '-0.1285', '-0.3438', '0.0319', '-0.355', '0.1346', '-0.00394', '0.3118', '0.11804', '-0.02103', '-0.1927', '0.1575', '-0.2168', '-0.0616', '0.3503', '0.1769', '-0.06076', '-0.0002272', '-0.2374', '0.01996', '-0.4067', '0.02574', '-0.3945', '0.02388', '-0.64', '0.2491', '-0.02255', '-0.3872', '-0.4797', '0.0766', '0.1194', '0.318', '0.02522', '-0.09686', '-0.354', '-0.1356', '0.002228', '-0.2338', '-0.3108', '0.6826', '0.01524', '-0.5244', '0.4617', '0.2769', '0.1164', '0.3596', '-0.193', '0.2', '0.02223', '0.293', '-0.0732', '-0.2498', '0.1218', '-0.2177', '-0.10693', '-0.1549', '-0.2286', '0.1562', '0.4268', '0.05103', '-0.06445', '-0.168', '0.1365', '0.3777', '-0.04254', '-0.1409', '0.1279', '0.07776', '0.154', '0.03064', '0.501', '0.478', '0.2983', '0.0841', '0.2122', '0.06323', '-0.2998', '0.5454', '0.4702', '0.3735', '-0.4856', '-0.1543', '0.03262']",C142171,,,,,,
mondo:0009614,"methylmalonic aciduria, cblB type","['methylmalonic acidemia, cblB type', 'methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB complementation type', 'vitamin B12-responsive methylmalonic acidemia type cblB', 'vitamin B12-responsive methylmalonic aciduria, type cblB', 'methylmalonic aciduria, vitamin B12-responsive, due to defect in synthesis of adenosylcobalamin, cblB type', 'methylmalonic aciduria cblB type', 'methylmalonic aciduria, cblB type', 'methylmalonic acidemia cblB type', 'methylmalonic aciduria, vitamin B12-responsive, cblB type']",0060743,251110,79311,C1855102,"['-0.2035', '0.338', '0.0744', '-0.0464', '0.1696', '-0.3115', '-0.305', '0.04916', '-0.3047', '-0.1134', '-0.1938', '-0.1312', '0.1908', '-0.2642', '-0.1202', '-0.2023', '-0.0863', '-0.2527', '-0.191', '-0.347', '0.02464', '-0.343', '0.2428', '0.007557', '0.2328', '0.122', '0.05212', '-0.10284', '0.07715', '-0.2295', '-0.0423', '0.2886', '0.2385', '-0.01055', '-0.07764', '-0.2231', '-0.03345', '-0.3723', '0.00706', '-0.2751', '0.02357', '-0.6763', '0.2019', '0.0899', '-0.343', '-0.4434', '0.1315', '0.1581', '0.285', '0.05307', '-0.1165', '-0.3594', '-0.1423', '-0.0907', '-0.1597', '-0.3704', '0.592', '0.05444', '-0.4673', '0.396', '0.3022', '0.1216', '0.4844', '-0.178', '0.1243', '0.03784', '0.3108', '-0.07666', '-0.2578', '0.1606', '-0.0938', '-0.1687', '-0.09515', '-0.1766', '0.2242', '0.4683', '0.02989', '-0.1467', '-0.09534', '0.1805', '0.2827', '-0.0692', '-0.1902', '0.0977', '0.0666', '0.1888', '0.0697', '0.4036', '0.5', '0.2261', '0.1903', '0.237', '0.07745', '-0.251', '0.4714', '0.5015', '0.3853', '-0.3416', '-0.2094', '0.002869']",C142172,,,,,,
mondo:0009615,methylmalonic acidemia due to methylmalonyl-CoA epimerase deficiency,"['MCEE deficiency', 'methylmalonyl-Coa epimerase deficiency with sepiapterin reductase deficiency', 'methylmalonyl-Coa racemase deficiency', 'methylmalonyl-CoA epimerase deficiency', 'methylmalonic aciduria III, formerly', 'methylmalonic aciduria III', 'methylmalonic aciduria due to methylmalonyl-CoA epimerase deficiency', 'methylmalonic acidemia due to methylmalonyl-CoA racemase deficiency', 'methylmalonic aciduria due to methylmalonyl-CoA racemase deficiency']",,251120,308425,C1855100,"['-0.75', '0.307', '-0.332', '0.03625', '-0.2166', '-0.04874', '-0.4617', '0.1925', '-0.06125', '0.678', '-0.475', '-0.2327', '0.1641', '0.281', '-0.1267', '-0.1702', '0.04825', '0.06335', '-0.2634', '-0.871', '0.06366', '-0.289', '0.6514', '0.06305', '0.10004', '-0.1313', '0.2217', '0.0536', '-0.0629', '-0.08545', '-0.1015', '0.1576', '0.766', '0.3564', '-0.33', '-0.1891', '-0.534', '-0.068', '-0.2297', '0.02173', '0.1543', '-0.4958', '0.596', '-0.2173', '-0.3289', '-0.05255', '0.051', '-0.2505', '-0.154', '0.3596', '-0.0934', '0.03223', '0.02032', '-0.3296', '-0.0744', '0.002337', '0.3071', '-0.3816', '-0.4202', '0.269', '0.2734', '-0.11487', '0.2852', '-0.3406', '-0.08075', '0.2803', '0.3655', '0.082', '-0.3418', '0.2336', '-0.3257', '0.2401', '-0.2573', '-0.2627', '0.04895', '0.377', '0.5117', '-0.1752', '0.3225', '0.04172', '0.1781', '-0.3489', '-0.311', '0.11475', '0.729', '0.504', '0.1768', '0.1763', '0.5283', '0.4087', '0.4678', '0.2827', '-0.3167', '-0.03455', '0.563', '0.8877', '0.11664', '-0.1775', '-0.2742', '0.4023']",,,C565386,,,,
mondo:0009616,"microcephalic primordial dwarfism, Toriello type","['microcephalic primordial dwarfism Toriello type', 'microcephalic primordial dwarfism, Toriello type', 'microcephalic primordial dwarfism and cataracts']",,251190,2643,C1855089,,,,C537321,,,,
mondo:0009617,"microcephaly 1, primary, autosomal recessive","['MCPH1', 'microcephaly 1, primary, autosomal recessive', 'premature chromosome condensation with microcephaly and intellectual disability', 'PCC syndrome', 'MCPH1 autosomal recessive primary microcephaly', 'premature chromosome condensation with microcephaly and mental retardation', 'premature chromosome condensation syndrome', 'autosomal recessive primary microcephaly caused by mutation in MCPH1']",0070285,251200,52183,C1855081,"['-0.1152', '0.3267', '0.3862', '-0.04358', '0.4275', '-0.1302', '0.2273', '0.527', '-1.04', '-0.3284', '-0.1098', '0.267', '0.402', '0.7583', '0.693', '-0.1523', '0.55', '0.5703', '-0.7847', '-1.137', '-0.2524', '0.00478', '0.2632', '-0.0483', '0.5093', '-0.05902', '-0.2133', '0.3057', '0.3523', '-0.1792', '-0.1984', '-0.697', '0.5186', '0.306', '-0.2554', '0.8423', '-0.3223', '-0.3105', '0.2151', '-0.3506', '-0.04755', '0.49', '-0.405', '-0.324', '0.1332', '-0.6167', '0.8667', '0.1328', '0.1164', '0.02866', '0.3271', '-0.5063', '-0.318', '-0.1431', '-0.1833', '0.1709', '-0.6177', '0.6636', '-0.3943', '0.339', '0.10864', '0.4976', '0.4265', '0.1589', '-0.1786', '0.1675', '0.4636', '-0.2107', '-1.379', '0.2014', '-0.5933', '0.9795', '0.3838', '-1.023', '-0.0844', '0.4336', '0.2438', '-0.2075', '-0.2399', '-0.05075', '-0.4282', '1.0', '-0.00659', '0.456', '0.1279', '-0.349', '0.4531', '-0.3682', '1.022', '0.872', '-0.1771', '0.1746', '-0.2053', '0.1952', '-0.12494', '0.5415', '0.6147', '-0.5415', '0.6504', '-0.7017']",,,C565384,,,,
mondo:0009618,microcephaly-cardiomyopathy syndrome,"['microcephaly with cardiomyopathy', 'severe microcephaly and self-limiting dilated cardiomyopathy', 'severe microcephaly with mental retardation and dilated cardiomyopathy', 'severe microcephaly with intellectual disability and dilated cardiomyopathy', 'microcephaly-cardiomyopathy', 'Winship-Viljoen-Leary syndrome']",,251220,2515,C1855080,,,,C536711,,,,
mondo:0009619,microcephaly-micromelia syndrome,"['MIMIS', 'microcephaly-micromelia syndrome']",,251230,572768,C1855079,"['-0.02748', '0.02028', '0.015045', '-0.007996', '0.004467', '-0.05045', '0.002026', '0.0465', '-0.03143', '-0.03583', '0.0005655', '0.00989', '0.001903', '0.01515', '-0.02306', '-0.02559', '0.01143', '-0.00562', '-0.008705', '-0.06696', '0.007202', '-0.009254', '0.02348', '-0.002619', '0.01308', '0.005417', '-0.02243', '-0.006676', '0.01634', '-0.01314', '0.02295', '-0.01071', '0.0531', '0.03717', '-0.0015545', '-0.01898', '0.00551', '-0.01715', '-0.01414', '-0.0349', '0.01851', '-0.02948', '0.009094', '-0.0203', '0.005375', '-0.02525', '-0.03522', '0.04297', '0.013336', '0.00776', '-0.02255', '0.00221', '0.01041', '0.01033', '-0.01964', '-0.009766', '0.00945', '-0.002632', '-0.0388', '-0.004948', '0.012314', '0.00686', '-0.002237', '-0.001011', '-0.00393', '0.0079', '0.02974', '0.03119', '-0.03162', '0.03934', '-0.0533', '0.004776', '0.009094', '-0.01959', '0.009964', '0.02354', '0.01776', '-0.01107', '-0.013565', '-0.02109', '-0.002287', '0.00235', '-0.01787', '0.04144', '-0.001903', '0.01187', '0.004498', '0.04736', '0.05685', '0.01349', '0.0202', '0.05026', '0.00709', '0.00982', '0.06177', '0.02731', '0.04553', '-0.0443', '0.01118', '0.02171']",,,C565382,,,,
mondo:0009620,Say-Barber-Miller syndrome,"['Say Barber Miller syndrome', 'microcephaly-hypogammaglobulinemia-abnormal immunity syndrome', 'microcephaly hypogammaglobulinemia abnormal immunity', 'microcephaly with chemotactic defect and transient hypogammaglobulinemia']",,251240,3132,,,,,C536618,,,,
mondo:0009621,microcephaly-cervical spine fusion anomalies syndrome,"['microcephaly, mild intellectual disability, short stature, and skeletal anomalies', 'microcephaly, mild mental retardation, short stature, and skeletal anomalies', 'microcephaly with cervical spine fusion anomalies', 'microcephaly cervical spine fusion anomalies']",,251250,2522,C0796066,,,,C537325,,,,
mondo:0009622,Jawad syndrome,"['microcephaly with intellectual disability and digital anomalies', 'JAWAD syndrome', 'Kelly syndrome', 'JWDS', 'Jawad syndrome', 'microcephaly with mental retardation and digital anomalies']",,251255,313795,C0796063,"['-0.2385', '-0.1758', '0.3542', '-0.318', '0.464', '-0.3027', '-0.1655', '0.3884', '-0.515', '-0.3413', '-0.1771', '0.2015', '0.11847', '-0.2177', '-0.176', '0.1252', '0.658', '-0.05322', '-0.1195', '-0.531', '0.003485', '0.2612', '0.2386', '-0.3167', '0.368', '0.02226', '-0.2382', '-0.01211', '0.318', '-0.315', '0.281', '-0.4482', '0.2325', '0.3496', '0.2583', '-0.0847', '-0.4211', '-0.1853', '-0.2766', '-0.2803', '0.2362', '-0.301', '-0.0522', '-0.04184', '0.1177', '-0.4678', '-0.0658', '0.569', '-0.1008', '-0.0632', '-0.4324', '0.0537', '-0.1462', '-0.0926', '-0.511', '-0.2404', '0.0816', '-0.01473', '-0.185', '-0.01859', '-0.000825', '-0.0983', '-0.3508', '0.3206', '-0.2842', '0.0633', '0.2042', '0.5737', '-0.3267', '0.3389', '-0.457', '0.1616', '0.3323', '-0.136', '-0.169', '-0.3555', '0.1747', '-0.2686', '-0.4346', '-0.2391', '0.06824', '-0.05545', '0.0857', '0.4563', '-0.02101', '-0.1914', '-0.3877', '0.713', '0.2251', '0.0658', '0.1392', '0.6787', '0.3325', '0.1575', '0.5127', '0.01733', '0.3389', '-0.6616', '0.674', '0.3005']",,,,,,,
mondo:0009623,Nijmegen breakage syndrome,"['Seemanova syndrome type 2', 'microcephaly, normal intelligence and immunodeficiency', 'AT V1', 'microcephaly-immunodeficiency-lymphoreticuloma syndrome', 'NBs', 'microcephaly with normal intelligence immunodeficiency and lymphoreticular malignancies', 'ataxia-telangiectasia variant V2', 'immunodeficiency, microcephaly, and chromosomal instability', 'Nijmegen breakage syndrome', 'Nonsyndromal microcephaly autosomal recessive with normal intelligence', 'Seemanova syndrome 2', 'microcephaly with normal intelligence, immunodeficiency, and lymphoreticular malignancies', 'microcephaly immunodeficiency lymphoreticuloma', 'Berlin breakage syndrome', 'immunodeficiency-microcephaly-chromosomal instability syndrome', 'ataxia-telangiectasia, variant 1', 'Nonsyndromal microcephaly, autosomal recessive, with normal intelligence', 'Seemanova syndrome', 'ataxia-telangiectasia variant V1']",7400,251260,647,CN860323,"['0.075', '-0.05356', '-0.1753', '-0.3872', '0.295', '-0.2593', '0.3972', '0.3594', '-0.295', '-0.5894', '0.556', '0.3093', '0.0891', '0.174', '-0.1854', '0.01253', '0.535', '-0.1498', '-0.1166', '-0.2238', '0.2291', '-0.1058', '0.5605', '0.09735', '0.1421', '-0.1727', '-0.5254', '0.3298', '0.1907', '-0.2793', '0.9136', '-0.2396', '0.3518', '-0.4429', '0.5854', '-0.12494', '-0.4377', '-0.2542', '-0.5415', '0.2505', '-0.00548', '0.181', '0.1879', '0.003273', '0.03073', '-0.402', '0.3071', '-0.2075', '0.269', '-0.0288', '0.1536', '-0.1271', '-0.335', '0.1718', '-0.2556', '-0.3013', '0.1635', '-0.5283', '0.03735', '0.3042', '0.0976', '0.2314', '-0.6177', '0.635', '0.4634', '0.1877', '0.2231', '0.1393', '-0.329', '0.666', '-0.1954', '0.1333', '0.0779', '0.4016', '0.0699', '0.05408', '0.4167', '-0.2411', '0.1996', '0.3123', '-0.05048', '-0.1427', '0.09595', '0.05704', '-0.2886', '-0.285', '0.1989', '0.3171', '0.302', '0.1181', '0.04596', '0.371', '-0.3003', '-0.3694', '0.722', '0.2693', '-0.1904', '-0.2183', '0.3318', '0.2275']",C4692,,D049932,,,10067857,
mondo:0009624,microcephaly and chorioretinopathy 1,"['microcephaly and chorioretinopathy caused by mutation in TUBGCP6', 'autosomal recessive chorioretinopathy-microcephaly syndrome', 'autosomal recessive chorioretinopathy-microcephaly-intellectual disability syndrome', 'microcephaly and chorioretinopathy, autosomal recessive, type 1', 'TUBGCP6 microcephaly and chorioretinopathy', 'MCCRP1', 'microcephaly and chorioretinopathy type 1', 'Pseudotoxoplasmosis syndrome', 'microcephaly and chorioretinopathy, autosomal recessive, 1']",0080105,251270,2518,,"['-0.1259', '0.1803', '0.672', '-0.0975', '0.3625', '0.05484', '-0.1266', '0.272', '-1.088', '-0.2617', '0.009796', '0.171', '0.4895', '-0.03613', '0.3674', '-0.4478', '0.947', '-0.00422', '-0.1902', '-0.5293', '-0.2837', '-0.0784', '-0.01877', '0.473', '0.1263', '0.579', '-0.2954', '0.41', '0.3306', '-0.3003', '-0.05386', '-0.3464', '0.845', '0.08887', '-0.402', '0.892', '-0.6978', '-0.4705', '-0.0367', '-0.3848', '0.0522', '0.2808', '-0.425', '-0.3743', '0.1984', '-0.544', '0.7925', '-0.047', '0.0423', '-0.2546', '0.399', '-0.6675', '-0.4443', '-0.2646', '0.2352', '0.04785', '-0.3828', '0.4458', '-1.002', '0.2898', '0.12006', '0.2588', '0.422', '0.2803', '0.014656', '0.04242', '0.6274', '0.2607', '-0.8315', '0.2013', '-0.675', '1.004', '0.2411', '-0.3882', '0.114', '0.3354', '0.658', '-0.1069', '-0.1885', '0.07306', '-0.1437', '0.627', '0.1816', '1.058', '-0.2169', '-0.06934', '0.2869', '-0.377', '0.7515', '0.7544', '-0.1302', '0.408', '-0.4426', '0.1288', '-0.2052', '0.1725', '1.127', '-0.1353', '1.014', '-0.4563']",C129306,,,,,,
mondo:0009625,diencephalic-mesencephalic junction dysplasia syndrome 1,"['DMJDS1', 'recessive microcephaly with spastic quadriplegia', 'microcephaly, seizures, spasticity, and brain calcifications', 'MISSBC', 'microcephaly with spastic quadriplegia']",,251280,,C1855055,,,,C537546,,,,
mondo:0009626,pseudo-TORCH syndrome,"['BLCPMG', 'Baraitser Brett Piesowicz syndrome', 'microcephaly-intracranial calcification-intellectual disability syndrome', 'bilateral band-like calcification with polymicrogyria', 'Baraitser-Brett-Piesowicz syndrome', 'band-like calcification with simplified gyration and polymicrogyria', 'congenital intrauterine infection-like syndrome', 'pseudo-TORCH syndrome', 'BLC-PMG', 'Baraitser-Reardon syndrome', 'microcephaly - intracranial calcification - intellectual disability', 'microcephaly intracranial calcification']",0050656,,1229,C3489725,"['-0.6514', '-0.2026', '-0.594', '-0.2467', '0.2573', '-0.2974', '0.5386', '0.1785', '-0.5356', '-0.574', '-0.4053', '-0.5015', '-0.4758', '-0.317', '0.5522', '0.535', '0.4214', '-0.4097', '-0.07117', '-0.9907', '0.4805', '0.02016', '-0.1519', '-0.682', '-0.2047', '-0.05023', '-0.6455', '0.01266', '-0.03717', '-0.5986', '0.396', '-0.03134', '0.4995', '0.638', '0.0923', '0.4612', '-0.5244', '-0.1412', '-0.4097', '0.313', '0.1862', '-0.1783', '0.511', '-0.2323', '0.257', '-0.8267', '-0.04626', '-0.113', '-0.743', '-0.03032', '0.1364', '-0.8027', '0.3467', '0.2764', '0.11163', '0.246', '0.2167', '-0.2668', '-0.4297', '0.0674', '-0.42', '0.04395', '0.5347', '-0.2822', '0.2391', '-0.2405', '0.3018', '0.4644', '-0.4365', '0.9927', '-0.601', '0.3325', '0.3958', '-0.04086', '0.3386', '-0.121', '0.393', '-0.0516', '0.1409', '0.00218', '-0.05716', '0.8003', '-0.1311', '-0.08276', '-0.05725', '-0.01289', '1.022', '0.734', '-0.2104', '0.3562', '0.451', '0.453', '0.2327', '0.1869', '0.4255', '0.3555', '0.539', '-0.223', '0.6797', '-0.4697']",,,,,,,
mondo:0009627,Galloway-Mowat syndrome,"['nephrosis-microcephaly syndrome', 'Galloway Mowat syndrome', 'nephrosis-neuronal dysmigration syndrome', 'microcephaly nephrosis syndrome', 'microcephaly, hiatal hernia and nephrotic syndrome', 'nephrosis neuronal dysmigration syndrome', 'Galloway syndrome', 'GAMOS', 'hiatal hernia-microcephaly-nephrosis, Galloway type', 'microcephaly, hiatal hernia, and nephrotic syndrome', 'Galloway-Mowat syndrome', 'cerebellar ataxia with intellectual disability, optic atrophy, and skin abnormalities', 'cerebellar ataxia with mental retardation, optic atrophy, and skin abnormalities', 'microcephaly-hiatus hernia-nephrotic syndrome', 'spinocerebellar ataxia, autosomal recessive 5, formerly', 'spinocerebellar ataxia, autosomal recessive 5']",0080694,,2065,C0795949,"['0.03687', '0.4868', '-0.01653', '0.01694', '-0.2385', '-0.844', '0.1807', '0.8013', '-1.093', '-0.499', '0.1095', '-0.2228', '-0.261', '0.04745', '-0.2256', '-0.0946', '0.6357', '-0.2517', '0.09644', '-0.3943', '0.6377', '-0.05154', '-0.05615', '-0.3125', '-0.076', '-0.661', '0.3623', '0.2139', '0.273', '-0.2573', '0.6045', '-0.02107', '0.886', '0.1725', '0.3184', '-0.3147', '-0.6694', '0.2627', '-0.4272', '0.1558', '-0.05374', '-0.2468', '0.03055', '0.00575', '0.1482', '-0.3623', '0.00902', '0.1103', '-0.7866', '-0.7183', '0.02309', '0.458', '0.244', '-0.1443', '-0.2844', '0.273', '-0.05518', '-0.05533', '-0.1082', '0.6694', '0.03003', '-0.279', '-0.015236', '0.02933', '-0.5557', '-0.2325', '0.712', '0.04495', '-0.2446', '0.56', '-0.2316', '-0.09686', '0.0434', '0.4731', '0.014786', '-0.0985', '0.731', '0.02516', '-0.3486', '-0.04758', '0.3733', '0.1798', '0.0798', '1.049', '-0.3647', '0.7183', '0.003489', '-0.1384', '0.0786', '0.576', '0.6504', '0.598', '-0.1436', '-0.3462', '0.1793', '-0.4658', '0.61', '-0.1427', '0.1467', '0.755']",C132195,,C537548,,,,
mondo:0009629,Desbuquois dysplasia 1,"['Desbuquois dysplasia caused by mutation in CANT1', 'micromelic dwarfism with vertebral and metaphyseal abnormalities and advanced carpotarsal ossification', 'Desbuquois dysplasia 1', 'desbuquois syndrome', 'Desbuquois dysplasia type 1', 'DBQD1', 'CANT1 Desbuquois dysplasia', 'Desbuquois dysplasia, Kim variant']",,251450,,C4012146,,,,,,,,
mondo:0009630,"microphthalmia, isolated, with coloboma 4","['microphthalmia, isolated, with coloboma 4', 'MCOPCB4', 'microphthalmia with colobomatous cyst', 'microphthalmia, isolated, with coloboma type 4']",,251505,,C1855053,,,,C565378,,,,
mondo:0009631,isolated microphthalmia 1,"['Mcop', 'microphthalmos, autosomal recessive', 'anophthalmia, clinical, isolated', 'isolated microphthalmia type 1', 'MCOP1', 'microphthalmia, isolated 1']",0060840,251600,2542,C1855052,"['-0.2913', '-0.4167', '-0.3542', '0.318', '0.424', '0.0727', '0.3127', '0.562', '-0.4592', '-0.508', '-0.08246', '-0.3428', '0.09314', '-0.102', '-0.2693', '-0.3162', '0.5664', '-0.623', '0.1272', '-1.172', '-0.4446', '-0.3174', '0.3054', '-0.1022', '-0.1318', '0.02705', '-0.333', '0.596', '0.4011', '0.604', '0.71', '-0.07367', '-0.0185', '0.47', '-0.0412', '0.4717', '0.1854', '-0.5273', '0.2446', '-1.091', '0.3555', '0.1547', '0.03412', '-0.712', '0.1766', '-0.127', '0.3293', '-0.3616', '-0.2844', '0.3464', '-0.356', '-0.21', '0.00859', '-0.822', '0.02126', '-0.1637', '0.4783', '0.11566', '-0.518', '0.1531', '0.295', '0.2094', '0.2397', '0.748', '-0.6387', '0.1609', '0.3933', '0.5728', '-0.1225', '0.3203', '0.1737', '0.0868', '0.1647', '0.002354', '0.11664', '-0.5054', '0.5', '-0.3472', '-0.5933', '-0.318', '0.0319', '0.2189', '0.0364', '0.7705', '-0.2368', '-0.8267', '0.2092', '0.2471', '-0.1561', '0.06137', '0.3838', '0.1873', '-0.3528', '-0.00956', '0.3115', '-0.6465', '0.3213', '-0.2786', '0.2118', '-0.156']",,,C565377,,,,
mondo:0009632,"microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies","['microphthalmia with hyperopia, retinal degeneration, macrophakia, and dental anomalies']",,251700,,C1968637,,,,C566884,,,,
mondo:0009633,"microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma","['MSPKA', 'microspherophakia and/or megalocornea, with ectopia lentis and with or without secondary glaucoma']",,251750,,C3538951,"['-0.1115', '0.05283', '0.05524', '-0.01709', '0.06076', '-0.03204', '0.0563', '0.1461', '-0.1359', '-0.1005', '-0.06647', '-0.0937', '-0.06064', '0.0183', '-0.2095', '-0.1409', '0.0349', '-0.0801', '0.00657', '-0.3096', '-0.01501', '0.01595', '0.0962', '-0.01458', '0.04575', '-0.01178', '-0.01984', '0.06097', '0.0941', '0.01444', '0.0842', '-0.0661', '0.1927', '0.0918', '0.02441', '-0.0542', '-0.03876', '-0.1301', '-0.03094', '-0.1897', '0.1129', '-0.0967', '0.11743', '-0.04254', '0.01142', '-0.0018215', '0.002377', '0.10394', '0.01855', '0.010605', '0.02264', '0.0524', '0.02115', '-0.054', '-0.04297', '-0.07336', '0.192', '-0.142', '-0.2408', '-0.03625', '0.1418', '0.049', '-0.07117', '0.04813', '-0.03079', '-0.05984', '0.1453', '0.152', '-0.0995', '0.10785', '-0.1621', '0.113', '0.04688', '-0.1796', '-0.02437', '-0.0438', '-0.003813', '-0.03125', '-0.1153', '-0.07733', '0.00921', '0.01099', '-0.05423', '0.1904', '-0.04147', '-0.01654', '0.04062', '0.1635', '0.05524', '0.0187', '-0.00637', '0.17', '-0.02483', '0.05484', '0.3835', '-0.03032', '0.1289', '-0.11035', '-0.01936', '0.0666']",,,,,,,
mondo:0009634,microtia with meatal atresia and conductive deafness,"['microtia meatal atresia deafness dominant', 'Gupta Patton syndrome', 'familial microtia and meatal atresia', 'familial microtia with meatal atresia and conductive deafness', 'microtia, meatal atresia and conductive deafness', 'microtia with meatal atresia and conductive deafness']",,251800,,C2931502,,,,C537469,,,,
mondo:0009635,microvillus inclusion disease,"['microvillus inclusion disease', 'Davidson^s disease', 'congenital familial protracted diarrhoea with enterocyte Brush-border abnormalities', 'microvillous inclusion disease', 'secretory diarrhea caused by mutation in MYO5B', 'MYO5B secretory diarrhoea', 'intractable diarrhoea of infancy', 'diarrhea 2, with microvillus atrophy', 'MVD', 'MVID', 'MYO5B secretory diarrhea', 'congenital familial protracted diarrhea with enterocyte brush-border abnormalities', 'diarrhoea 2 with microvillus atrophy', 'microvillus atrophy, congenital', 'congenital familial protracted diarrhea', 'familial enteropathy, microvillus', 'congenital familial protracted diarrhoea with enterocyte brush-border abnormalities', 'congenital familial protracted diarrhea with enterocyte Brush-border abnormalities', 'Davidson disease', 'intractable diarrhea of infancy', 'secretory diarrhoea caused by mutation in MYO5B', 'diarrhoea 2, with microvillus atrophy', 'congenital microvillous atrophy', 'congenital microvillus atrophy', 'DIAR2', 'congenital familial protracted diarrhoea', 'diarrhea 2 with microvillus atrophy']",0060775,251850,2290,C0341306,"['-0.4817', '-0.1616', '-0.1473', '0.2822', '0.337', '-0.742', '-0.5103', '0.676', '-0.1554', '-0.045', '-0.6074', '-0.9526', '-0.4646', '0.1366', '-0.4692', '-0.03165', '0.1719', '0.4167', '-0.2979', '-1.324', '0.2032', '-0.7134', '0.3843', '-0.3818', '0.3706', '-0.02332', '-0.283', '0.3064', '-0.01714', '-0.4785', '0.327', '0.1793', '0.1686', '-0.0597', '0.3499', '0.02164', '-0.2905', '-0.309', '0.1399', '0.4136', '0.2756', '-0.1334', '-0.0971', '-0.56', '0.371', '-0.131', '-0.6216', '-0.2732', '-0.4875', '0.5044', '-0.4202', '-0.1989', '-0.003986', '-0.1449', '-0.2874', '-0.4136', '-0.2406', '-0.4436', '-0.515', '0.1238', '0.8115', '0.2488', '0.11914', '-0.6284', '0.2129', '-0.5796', '0.6626', '-0.02492', '-0.439', '0.6616', '0.297', '-0.2019', '0.06757', '-0.10864', '0.3079', '-0.0702', '0.1395', '0.04337', '-0.1658', '0.1484', '-0.02629', '0.00506', '-0.2479', '-0.208', '0.0809', '0.345', '0.0776', '0.05753', '0.0787', '-0.2568', '0.832', '-0.2737', '0.1516', '0.2107', '0.01468', '0.2893', '0.4844', '-0.5786', '0.1782', '0.0191']",,,,579.8,,10068494,
mondo:0009636,mitochondrial DNA depletion syndrome 3 (hepatocerebral type),"['MTDPS3', 'mitochondrial DNA depletion syndrome 3 (hepatocerebral type)', 'mitochondrial DNA depletion syndrome type 3', 'DGUOK mitochondrial DNA depletion syndrome', 'mitochondrial DNA depletion syndrome caused by mutation in DGUOK', 'mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency']",0080121,251880,279934,C4310935,"['-0.6235', '0.167', '0.2054', '0.537', '-0.2546', '-0.561', '0.1638', '0.997', '-0.1941', '-0.3713', '-0.3137', '-0.4377', '-0.2064', '0.12006', '-0.385', '-0.0821', '-0.1929', '-0.263', '-0.09375', '-0.8613', '0.3552', '-0.613', '0.5244', '-0.08215', '-0.0672', '-0.0711', '-0.04053', '-0.001951', '-0.3208', '-0.1567', '0.354', '0.916', '0.0813', '-0.11127', '0.311', '-0.696', '-0.599', '0.074', '0.04153', '0.2598', '-0.2668', '-0.00492', '-0.2476', '0.4739', '-0.526', '0.0673', '-0.0831', '-0.3162', '-0.2152', '0.005447', '-0.3098', '-0.1895', '0.164', '-0.0686', '-0.03836', '-0.1841', '0.4087', '-0.02446', '-0.3716', '0.6284', '0.3665', '0.2031', '0.2634', '-0.1416', '-0.0848', '-0.1664', '0.3638', '0.04776', '0.06042', '0.484', '-0.2438', '0.1217', '0.05194', '0.4924', '0.0919', '-0.0908', '0.2184', '-0.5083', '-0.3936', '0.4067', '0.06586', '-0.1539', '-0.2676', '0.0409', '0.1963', '0.3323', '0.408', '-0.2288', '1.001', '0.2488', '1.187', '0.2761', '-0.2355', '-0.3835', '0.1772', '0.3926', '0.2079', '-0.547', '-0.194', '-0.3552']",,,,,,,
mondo:0009637,inborn mitochondrial myopathy,"['mitochondrial myopathy', 'mitochondrial cytopathy']",699,,206966,C0162670,"['-0.021', '0.3926', '-0.119', '0.509', '0.2598', '0.05798', '0.05978', '-0.1099', '-0.315', '-0.2651', '-0.1893', '-0.5767', '0.0511', '0.6733', '-0.207', '-0.1141', '-0.627', '0.12244', '-0.863', '-0.3862', '0.00904', '-0.1167', '0.3018', '-0.0935', '0.07404', '-0.6445', '-0.3987', '-0.01572', '-0.06094', '0.1881', '0.1389', '-0.1569', '0.279', '-0.02348', '0.214', '0.04526', '-0.4607', '0.5117', '0.3877', '-0.4724', '-0.376', '-0.407', '-0.4648', '0.11066', '-0.0513', '-0.4585', '0.1783', '0.2142', '0.5703', '-0.10144', '-0.046', '0.00967', '0.6157', '-0.02731', '0.4639', '-0.1722', '0.0296', '0.5215', '-0.1351', '0.1777', '0.4795', '-0.1192', '0.3726', '0.1095', '-0.7163', '0.1658', '0.19', '0.3997', '-0.3552', '0.01466', '0.2598', '0.2323', '-0.217', '-0.010254', '0.2654', '0.692', '-0.2219', '0.2251', '-0.2617', '-0.2203', '0.006348', '-0.3188', '-0.3818', '0.1288', '-0.0489', '0.1777', '-0.03244', '0.07733', '0.8506', '0.3577', '0.531', '-0.1498', '-0.4429', '0.1063', '0.2095', '0.5913', '-0.4023', '-0.3206', '-0.3699', '0.09094']",C101328,,D017240,,,10027710,
mondo:0009638,mitochondrial myopathy with a defect in mitochondrial-protein transport,['mitochondrial myopathy with a defect in mitochondrial-protein transport'],,251945,,C1855034,,,,C565376,,,,
mondo:0009642,orofaciodigital syndrome type II,"['oral facial digital syndrome type 2', 'orofaciodigital syndrome 2', 'oral facial digital syndrome 2', 'orofaciodigital syndrome type 2', 'oral-facial-digital syndrome type 2', 'MOHR syndrome', 'Ofds 2', 'OFD2', 'Mohr syndrome', 'orofaciodigital syndrome II', 'oral-Facial-digital syndrome, type 2', 'OFD syndrome 2']",,252100,2751,,,,,,759.89,,,
mondo:0009643,sulfite oxidase deficiency due to molybdenum cofactor deficiency type A,"['molybdenum cofactor deficiency type A', 'molybdenum cofactor deficiency, complementation group A', 'molybdenum cofactor deficiency complementation group A', 'molybdenum cofactor deficiency, complementation group type a', 'MOCODA', 'sulfite oxidase, xanthine dehydrogenase, and aldehyde oxidase, combined deficiency of', 'combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type A', 'MOCOD type A', 'molybdenum cofactor deficiency A']",0111164,252150,308386,C1854988,"['-0.3257', '0.3198', '0.1682', '-0.0842', '0.08636', '-0.418', '-0.05804', '0.0625', '-0.2566', '-0.2046', '-0.1226', '-0.0737', '0.0739', '-0.221', '0.0634', '0.1697', '-0.01703', '-0.0366', '-0.2412', '-0.4387', '0.0761', '-0.1937', '0.2397', '0.04755', '0.05533', '0.02298', '-0.0003624', '-0.0985', '0.08466', '-0.1948', '0.1938', '0.323', '0.2717', '0.1116', '-0.0636', '-0.198', '0.0927', '-0.067', '-0.05786', '-0.2605', '0.0335', '-0.346', '0.0957', '0.0729', '-0.2578', '-0.321', '0.12354', '0.0598', '0.11847', '0.1643', '-0.1884', '-0.1589', '-0.1293', '0.03041', '-0.11456', '-0.3', '0.3242', '0.06976', '-0.2101', '0.3772', '0.05225', '0.11285', '0.2542', '-0.1318', '0.1715', '0.005657', '0.1621', '-0.06396', '-0.3757', '0.1389', '-0.3809', '0.02457', '0.002', '-0.03604', '0.05237', '0.3179', '0.2144', '-0.04495', '-0.1995', '0.1819', '0.343', '0.0889', '-0.139', '0.1805', '0.0709', '0.1885', '0.1724', '0.4158', '0.4497', '0.106', '0.0483', '0.2683', '0.00285', '-0.2007', '0.4663', '0.482', '0.1793', '-0.376', '0.2498', '0.03476']",,,C565372,,,,
mondo:0009644,sulfite oxidase deficiency due to molybdenum cofactor deficiency type B,"['molybdenum cofactor deficiency type B', 'molybdenum cofactor deficiency, complementation group type B', 'MOCOD type B', 'molybdenum cofactor deficiency complementation group B', 'MOCODB', 'molybdenum cofactor deficiency, complementation group B', 'molybdenum cofactor deficiency B', 'combined deficiency of sulfite oxidase, xanthine dehydrogenase and aldehyde oxidase type B']",0111163,252160,308393,C1854989,"['-0.2101', '0.148', '0.0837', '0.0426', '0.11755', '-0.1522', '0.01778', '-0.003386', '-0.0349', '-0.0697', '-0.07324', '0.0008054', '0.0041', '-0.01913', '-0.0344', '-0.05344', '-0.06024', '-0.01224', '-0.1749', '-0.2686', '0.01784', '-0.146', '0.2393', '-0.002449', '-0.02652', '-0.02524', '0.000793', '-0.0724', '-0.03268', '-0.1619', '0.1233', '0.1543', '0.1509', '0.1309', '0.06903', '-0.2141', '0.0278', '-0.0673', '-0.01862', '-0.1974', '-0.01773', '-0.278', '0.05954', '-0.03867', '-0.1503', '-0.1909', '0.0943', '0.06415', '0.05093', '0.1306', '0.0005455', '-0.1915', '0.001279', '0.04553', '-0.1816', '-0.04834', '0.2288', '-0.12274', '-0.2245', '0.079', '0.00892', '0.06067', '0.11163', '-0.01775', '0.1197', '0.04718', '0.2074', '-0.010086', '-0.1781', '0.08624', '-0.1595', '-0.0469', '-0.04156', '-0.1398', '0.1373', '0.1844', '0.04352', '-0.1179', '-0.0939', '0.0694', '0.02791', '0.0002129', '-0.0994', '0.06525', '0.06366', '0.002657', '0.1118', '0.175', '0.3386', '-0.03017', '0.12396', '0.1263', '-0.0334', '-0.0957', '0.282', '0.2375', '0.0989', '-0.3389', '0.007507', '0.0729']",,,C565373,,,,
mondo:0009645,chronic mucocutaneous candidiasis due to monocyte chemotactic disorder,['monocyte chemotactic disorder'],,252250,,C1854982,,,,C565371,,,,
mondo:0009646,monosomy 7 myelodysplasia and leukemia syndrome 1,"['myelodysplasia and leukemia syndrome with monosomy 7', 'monosomy 7 of bone marrow', 'myelodysplasia and leukaemia syndrome with monosomy 7', 'chromosome 7Q deletion', 'M7MLS1']",,252270,,C1854978,,C176908,,C565370,,,,
mondo:0009647,Morquio syndrome C,"['Morquio syndrome type C', 'Morquio syndrome C', 'Morquio syndrome, Nonkeratosulfate-Excreting type']",,252300,,,,,,C536247,,,,
mondo:0009648,peripheral motor neuropathy-dysautonomia syndrome,"['motor neuropathy, peripheral, with dysautonomia', 'Lisker-Garcia-Ramos syndrome']",,252320,2400,C1854961,,,,C536988,,,,
mondo:0009649,moyamoya disease 1,"['spontaneous occlusion of the circle of Willis', 'Moyamoya disease 1', 'Moyamoya disease', 'MYMY1']",,252350,,,,,,C536991,437.5,,,
mondo:0009650,mucolipidosis type II,"['inclusion cell disease', 'mucolipidosis 2 alpha/beta', 'mucolipidosis type II alpha/beta', 'mucolipidosis II', 'ML disorder type 2', 'N-acetylglucosamine 1phosphotransferase deficiency', 'ML 2 Alpha/Beta', 'Leroy disease', 'I cell disease', 'GNPTA', 'mucolipidosis type II', 'N-acetylglucosamine 1-phosphotransferase deficiency', 'I-cell disease', 'mucolipidosis II alpha/beta', 'mucolipidosis 2', 'ML 2']",0080070,252500,576,C2673377,"['-0.1471', '-0.2122', '0.4373', '-0.04242', '-0.288', '-0.774', '0.4617', '1.483', '-0.39', '-0.35', '-0.2118', '-0.05417', '-0.09015', '0.1196', '-0.077', '0.174', '0.1305', '-0.10864', '-0.4524', '-0.395', '0.03302', '-0.3909', '0.5654', '-0.01717', '-0.367', '-0.2515', '-0.3406', '0.3394', '-0.2072', '0.04724', '0.603', '0.4167', '-0.1505', '0.11725', '-0.4478', '-0.0224', '0.10034', '-0.02692', '0.5522', '0.07886', '0.3486', '-0.613', '-0.1378', '0.4897', '0.1304', '0.2307', '0.0872', '0.2179', '-0.586', '-0.2478', '-0.4097', '0.02954', '0.0851', '0.1603', '0.5566', '-0.0577', '-0.1705', '-0.012726', '0.5713', '0.0902', '0.07947', '0.1469', '-0.7666', '0.1804', '-0.2239', '-0.00399', '0.681', '-0.0162', '-0.4104', '0.1312', '-0.6045', '-0.10803', '-0.1395', '-0.1934', '-0.111', '0.3586', '0.04776', '-0.1334', '-0.4558', '-0.2289', '0.00599', '-0.4387', '-0.5273', '0.1283', '-0.3767', '0.4834', '-0.01102', '0.06714', '0.3167', '-0.1271', '0.3281', '-0.1115', '0.0862', '0.02902', '0.5117', '0.314', '0.2979', '-0.6577', '0.4646', '0.03906']",C61270,,C538602,,,,
mondo:0009652,GNPTG-mucolipidosis,"['GNPTG-mucolipidosis', 'ML 3C', 'mucolipidosis 3 gamma', 'mucolipidosis III gamma', 'mucolipidosis III, Iranian variant form', 'mucolipidosis III, variant form', 'mucolipidosis 3C', 'mucolipidosis III, complementation group C', 'mucolipidosis type III gamma', 'ML III gamma', 'ML 3 gamma', 'mucolipidosis type 3 gamma']",0080678,252605,423470,C1854896,,C129978,,C565367,,,,
mondo:0009653,mucolipidosis type IV,"['ML IV', 'ganglioside neuraminidase deficiency', 'Berman syndrome', 'sialolipidosis', 'MLIV', 'mucolipidosis type IV', 'mucolipidosis 4', 'ganglioside sialidase deficiency', 'mucolipidosis type 4', 'ML4', 'mucolipidosis IV', 'ML 4']",0080490,252650,578,CN716584,"['-0.632', '0.603', '-0.10187', '0.1257', '0.08167', '-0.885', '-0.2825', '0.4104', '-0.534', '-0.4917', '-0.4536', '0.2067', '0.1766', '0.1364', '-0.1142', '0.01418', '0.3066', '-0.437', '-0.1175', '-0.4595', '-0.156', '-0.3816', '0.644', '0.2737', '0.1459', '-0.2493', '-0.11255', '0.6', '-0.648', '0.496', '0.891', '-0.00793', '-0.1471', '-0.02983', '0.03333', '0.10767', '0.194', '-0.096', '-0.2192', '0.3638', '0.04715', '0.08844', '0.1608', '0.2708', '0.222', '-0.1516', '0.481', '-0.0523', '-0.1295', '-0.54', '0.5884', '0.1924', '-0.2913', '-0.554', '0.3975', '-0.477', '0.9', '-0.2155', '-0.5503', '0.5156', '0.1702', '-0.1279', '-0.2573', '0.1932', '0.2192', '-0.01108', '0.6147', '-0.2241', '-0.392', '0.2334', '-0.606', '-0.6484', '0.01877', '0.2646', '0.3162', '0.2734', '0.1189', '0.334', '-0.3318', '0.357', '0.2289', '-0.6997', '-0.2705', '0.7227', '-0.51', '-0.3518', '0.11975', '0.4443', '0.473', '0.287', '0.2214', '-0.164', '-0.0962', '-0.08307', '0.664', '0.325', '0.2886', '-0.3098', '0.012634', '-0.225']",C84896,,,,,,
mondo:0009655,mucopolysaccharidosis type 3A,"['MPS IIIA', 'mucopolysaccharidosis type IIIA (Sanfilippo A)', 'heparane sulfamidase deficiency', 'MPS III A', 'MPS3A', 'heparan sulfamidase deficiency', 'mucopoly-saccharidosis type 3A', 'heparan sulphate sulfatase deficiency', 'sulfamidase deficiency', 'MPS 3A', 'Sanfilippo A', 'mucopolysaccharidosis, type IIIA', 'Sanfilippo syndrome a', 'Sanfilippo syndrome type A', 'MPSIIIA', 'heparan sulfate sulfatase deficiency', 'mucopolysaccharidosis type IIIA', 'mucopolysaccharidosis, type 3A', 'mucopolysaccharidosis type 3A']",0111395,252900,79269,C0086647,"['-0.2449', '0.3357', '0.2979', '-0.1373', '0.09644', '-0.298', '-0.0332', '0.1254', '-0.2437', '0.01936', '-0.2678', '-0.0846', '0.0352', '-0.0772', '0.1703', '-0.0678', '0.0003388', '0.072', '-0.3208', '-0.3955', '0.05582', '-0.26', '0.1755', '-0.1085', '-0.02739', '-0.09625', '0.04266', '-0.1853', '0.01622', '-0.10266', '0.1228', '0.1554', '0.2559', '0.12256', '-0.10516', '-0.1063', '-0.01805', '-0.29', '-0.0426', '-0.3367', '0.1793', '-0.386', '0.0736', '0.1847', '-0.0714', '-0.3716', '0.09656', '0.1158', '0.1274', '0.336', '-0.1444', '0.163', '-0.1193', '-0.01863', '0.2299', '-0.3403', '0.1697', '-0.12103', '-0.3699', '0.0878', '0.1847', '0.02951', '0.198', '-0.002722', '0.04004', '-0.01052', '0.0969', '-0.1339', '-0.2566', '-0.03363', '-0.589', '-0.084', '-0.1255', '0.0341', '0.07715', '0.2712', '0.0703', '-0.01094', '-0.2695', '-0.1493', '0.2446', '-0.1005', '-0.2378', '0.2966', '0.3123', '0.10297', '0.2198', '0.2297', '0.3547', '0.165', '0.1543', '0.3167', '0.0134', '-0.05838', '0.258', '0.364', '0.1815', '-0.36', '0.352', '0.1459']",C84897,,,,,,
mondo:0009656,mucopolysaccharidosis type 3B,"['Mucopoly-saccharidosis type 3B', 'Sanfilippo syndrome type B', 'Sanfilippo B', 'MPS IIIB', 'N-Acetyl-Alpha-D-glucosaminidase deficiency', 'MPSIIIB', 'Sanfilippo syndrome B', 'mucopolysaccharidosis type IIIB', 'mucopolysaccharidosis type IIIB (Sanfilippo B)', 'MPS3B', 'mucopolysaccharidosis, type 3B', 'MPS 3B', 'N-acetyl-alpha-glucosaminidase deficiency', 'mucopolysaccharidosis, type IIIB', 'NAGLU deficiency', 'MPS III B', 'mucopolysaccharidosis type 3B']",0111394,252920,79270,C0086648,"['-0.1572', '0.2854', '0.196', '-0.1162', '0.1268', '-0.2634', '-0.0394', '0.1543', '-0.2505', '-0.07153', '-0.2302', '-0.0352', '-0.03647', '-0.05515', '0.11206', '-0.09906', '-0.02252', '0.11316', '-0.35', '-0.397', '0.0599', '-0.2097', '0.1272', '-0.1204', '-0.04602', '-0.0579', '0.05823', '-0.124', '0.02579', '-0.1266', '0.1787', '0.1692', '0.2913', '0.0481', '-0.0853', '-0.0736', '-0.02567', '-0.3381', '-0.07086', '-0.278', '0.1205', '-0.329', '0.01976', '0.1339', '-0.1169', '-0.3232', '0.04672', '0.1383', '0.1573', '0.2089', '-0.0924', '0.1283', '-0.1729', '-0.0697', '0.1512', '-0.3074', '0.10455', '-0.1453', '-0.3838', '-0.01662', '0.1726', '-0.01166', '0.2079', '0.02335', '0.048', '0.05246', '0.11743', '-0.0643', '-0.2795', '0.04257', '-0.6143', '-0.0848', '-0.09235', '-0.02666', '0.2001', '0.1997', '0.04626', '0.02144', '-0.2373', '-0.0997', '0.1979', '-0.1299', '-0.1962', '0.1976', '0.3135', '0.1266', '0.2742', '0.2068', '0.3806', '0.1636', '0.1564', '0.3105', '0.00746', '-0.0662', '0.2405', '0.2922', '0.1544', '-0.4238', '0.3137', '0.1455']",C84898,,,,,,
mondo:0009657,mucopolysaccharidosis type 3C,"['mucopolysaccharidosis, type IIIC', 'Sanfilippo syndrome C', 'Sanfilippo syndrome type C', 'mucopolysaccharidosis type 3C', 'mucopolysaccharidosis, type 3C', 'MPSIIIC', 'mucopolysaccharidosis type IIIC (Sanfilippo C)', 'Sanfilippo C', 'HGSNAT deficiency', 'MPS IIIC', 'MPS III C', 'MPS3C', 'acetyl-CoA:alpha-glucosaminide N-acetyltransferase deficiency', 'MPS 3C', 'mucopolysaccharidosis type IIIC', 'Acetyl-CoA alpha-glucosaminide n-acetyltransferase deficiency', 'heparan-alpha-glucosaminide N-acetyltransferase deficiency', 'Mucopoly-saccharidosis type 3C']",0111393,252930,79271,C0086649,"['-0.1337', '0.3013', '0.249', '-0.09705', '0.03928', '-0.265', '-0.1373', '0.0986', '-0.2776', '0.03833', '-0.202', '-0.06085', '-0.011055', '0.003075', '0.0724', '-0.05786', '-0.0686', '0.1366', '-0.3413', '-0.3394', '0.04092', '-0.2566', '0.0525', '-0.1036', '-0.0654', '-0.0308', '0.04718', '-0.1322', '0.1259', '-0.1681', '0.1345', '0.1359', '0.3162', '0.0683', '-0.0335', '-0.0917', '-0.03204', '-0.3376', '-0.04672', '-0.3022', '0.1381', '-0.3389', '0.0485', '0.11365', '-0.05646', '-0.38', '0.1002', '0.1862', '0.2273', '0.2059', '-0.1104', '0.1149', '-0.19', '-0.0548', '0.1326', '-0.3806', '0.10614', '-0.1272', '-0.3794', '0.03268', '0.1455', '-0.01672', '0.211', '0.04724', '0.10114', '0.0188', '0.12256', '-0.09546', '-0.2908', '-0.03546', '-0.5913', '-0.05862', '-0.202', '-0.0493', '0.2239', '0.2314', '-0.02028', '0.112', '-0.1763', '-0.0399', '0.2898', '-0.1854', '-0.1979', '0.1757', '0.439', '0.1248', '0.196', '0.259', '0.4153', '0.1489', '0.0437', '0.2727', '-0.0649', '-0.0929', '0.3088', '0.3489', '0.1626', '-0.2793', '0.3118', '0.1508']",C84899,,,,,,
mondo:0009658,mucopolysaccharidosis type 3D,"['N-acetylglucosamine-6-sulfate sulfatase deficiency', 'MPS 3D', 'N-acetylglucosamine-6-sulfatase deficiency', 'MPS III D', 'mucopolysaccharidosis type IIID', 'mucopolysaccharidosis, type 3D', 'GNS deficiency', 'MPSIIID', 'Sanfilippo syndrome type D', 'mucopolysaccharidosis, type IIID', 'Sanfilippo syndrome D', 'MPS IIID', 'Sanfilippo D', 'mucopolysaccharidosis type 3D', 'glucosamine N-acetyl-6-sulfatase deficiency', 'Mucopoly-saccharidosis type 3D', 'MPS3D']",0111402,252940,79272,C0086650,"['-0.1162', '0.2328', '0.2234', '-0.0906', '0.1516', '-0.1881', '-0.02466', '0.1559', '-0.2869', '-0.0728', '-0.1869', '-0.0472', '-0.06476', '0.014946', '0.1266', '-0.1411', '-0.003574', '0.1046', '-0.322', '-0.3901', '0.0625', '-0.249', '0.0812', '-0.1224', '-0.0327', '-0.0193', '-0.003159', '-0.1219', '0.077', '-0.1263', '0.0651', '0.0744', '0.295', '0.03186', '-0.1048', '-0.1244', '0.02115', '-0.3313', '0.003382', '-0.2634', '0.1305', '-0.3418', '0.10596', '0.1058', '-0.06143', '-0.3484', '0.05215', '0.1469', '0.10504', '0.2175', '-0.141', '0.1285', '-0.1089', '0.03577', '0.1128', '-0.3467', '0.0909', '-0.1776', '-0.3335', '-0.03256', '0.2145', '-0.012474', '0.2173', '-0.03638', '0.06305', '0.0526', '0.1451', '-0.04178', '-0.255', '0.02808', '-0.458', '-0.05554', '-0.0519', '-0.05313', '0.1039', '0.2206', '0.02222', '0.08655', '-0.1782', '-0.1377', '0.1594', '-0.1301', '-0.191', '0.2566', '0.276', '0.098', '0.1921', '0.1366', '0.4343', '0.2668', '0.1656', '0.2932', '-0.05197', '-0.0731', '0.2712', '0.2778', '0.1489', '-0.3286', '0.2288', '0.1793']",C84900,,,,,,
mondo:0009659,mucopolysaccharidosis type 4A,"['MPS IV A', 'MPSIVA', 'mucopolysaccharidosis IVA', 'Morquio A disease', 'GALNS deficiency', 'mucopolysaccharidosis, type IVA', 'mucopolysaccharidosis type IVA', 'MPS IVA', 'MPS4A', 'N-acetylgalactosamine-6-sulfate sulfatase deficiency', 'galactosamine-6-sulfatase deficiency', 'mucopolysaccharidosis, type 4A', 'Morquio disease type A', 'Morquio syndrome A', 'MPS 4A']",0111391,253000,309297,,"['-0.1539', '0.323', '0.1794', '-0.003937', '0.1063', '-0.2064', '-0.02817', '0.146', '-0.308', '-0.04544', '-0.11584', '0.01129', '-0.1043', '-0.0636', '-0.01261', '-0.1089', '-0.08167', '-0.1102', '-0.3215', '-0.3396', '0.10486', '-0.1321', '0.3093', '0.04752', '-0.1918', '-0.06903', '-0.001182', '-0.0785', '-0.05112', '-0.0947', '0.3186', '0.1644', '0.288', '0.02805', '-0.02545', '-0.2114', '-0.04404', '-0.1617', '-0.0779', '-0.2142', '0.05612', '-0.3423', '0.2405', '0.1169', '-0.1349', '-0.1517', '0.0847', '0.02571', '0.12354', '0.11646', '0.0479', '0.003618', '-0.02147', '-0.162', '-0.03014', '-0.2937', '0.0856', '0.02206', '-0.3499', '-0.02914', '0.1956', '0.03122', '0.182', '-0.00967', '0.04843', '0.08167', '0.2324', '0.002333', '-0.326', '0.06757', '-0.3887', '-0.1201', '-0.0161', '-0.009', '0.23', '0.2308', '0.02477', '0.2676', '-0.2023', '-0.2355', '-0.05698', '-0.2042', '-0.08636', '0.4177', '0.02753', '0.02309', '0.3728', '0.09985', '0.1216', '0.07355', '0.08954', '0.1304', '0.1145', '-0.1819', '0.4617', '0.4001', '0.2673', '-0.4087', '0.1361', '0.0701']",C84901,,,,,,
mondo:0009660,mucopolysaccharidosis type 4B,"['mucopolysaccharidosis type IVB (Morquio)', 'MPS IV B', 'mucopolysaccharidosis type IVB', 'mucopolysaccharidosis, type 4B', 'MPSIVB', 'Morquio disease type B', 'MPS IVB', 'mucopolysaccharidosis, type IVB', 'Beta-D-galactosidase deficiency', 'Morquio syndrome B', 'MPS 4B', 'MPS4B']",0111392,253010,309310,C0086652,"['-0.1481', '0.287', '0.234', '-0.0676', '0.2151', '-0.1765', '-0.01169', '0.2261', '-0.1597', '-0.1515', '-0.0337', '0.1488', '-0.005497', '-0.0368', '-0.04977', '-0.0651', '-0.03534', '-0.00955', '-0.3396', '-0.4087', '0.03952', '-0.1333', '0.361', '-0.02113', '-0.03207', '-0.002766', '0.02684', '-0.0823', '0.0442', '-0.1533', '0.1991', '0.1353', '0.2283', '0.07495', '-0.0709', '-0.2769', '0.08246', '-0.1932', '-0.011406', '-0.2402', '0.00883', '-0.3003', '0.11786', '0.1658', '-0.2144', '-0.2053', '0.02771', '0.1145', '0.2847', '-0.03476', '0.00818', '-0.176', '0.06946', '-0.04837', '0.07336', '-0.412', '0.03253', '-0.1014', '-0.2189', '-0.01326', '0.1891', '0.0699', '0.076', '-0.1027', '0.09045', '-0.02342', '0.1611', '0.008995', '-0.29', '0.0204', '-0.3447', '-0.1742', '0.02817', '0.02946', '0.1736', '0.2058', '-0.04504', '0.06223', '-0.2197', '-0.1184', '0.03683', '-0.0104', '-0.08856', '0.188', '0.00833', '0.1544', '0.2651', '0.1721', '0.3145', '0.1509', '-0.02737', '0.2399', '0.04126', '-0.12335', '0.509', '0.214', '0.2441', '-0.3345', '0.083', '0.0955']",C84902,,,,,,
mondo:0009661,mucopolysaccharidosis type 6,"['mucopolysaccharidosis type VI', 'mucopolysaccharidosis type VI (Maroteaux-Lamy)', 'ARSB deficiency', 'N-acetylgalactosamine-4-sulfatase deficiency', 'arylsulfatase B deficiency', 'MPS 6', 'MPSVI', 'mucopolysaccharidosis VI', 'MPS VI', 'Mucopoly-saccharidosis type VI', 'MPS6', 'Maroteaux - Lamy syndrome', 'Maroteaux-Lamy disease', 'Maroteaux Lamy syndrome', 'deficiency of N-acetylgalactosamine-4-sulfatase', 'Arsb deficiency', 'N-acetylgalactosamine 4-sulfatase deficiency', 'MPS VI - Maroteaux-Lamy syndrome', 'Maroteaux-Lamy syndrome', 'ASB deficiency']",12800,253200,583,C0026709,"['-0.2133', '0.5205', '0.0711', '0.383', '0.6733', '-0.08826', '0.571', '0.6084', '-0.3062', '-0.4268', '0.247', '-0.1633', '-0.5376', '0.01709', '-0.1487', '-0.443', '0.04645', '-0.1578', '-0.11255', '-0.536', '0.1295', '-0.579', '0.4053', '-0.5503', '0.1908', '-0.4749', '0.585', '0.2637', '-0.64', '0.0913', '0.771', '0.384', '0.03876', '-0.2135', '-0.02724', '-1.184', '-0.3245', '-0.734', '0.3904', '-0.2279', '0.09766', '-0.7524', '0.797', '0.4841', '-0.05884', '-0.175', '0.2009', '-0.4175', '-0.4355', '-0.0109', '0.5303', '0.2678', '-0.3147', '-0.3916', '0.334', '-0.132', '-0.2803', '-0.4263', '0.3281', '-0.316', '-0.04745', '0.316', '-0.579', '0.3733', '0.1558', '-0.3958', '0.751', '0.3276', '-0.1938', '-0.01857', '-1.031', '-0.4214', '0.2517', '-0.3347', '0.4717', '0.1707', '0.291', '0.2151', '-0.5747', '-0.04456', '-0.02469', '-0.3616', '-0.4258', '0.8804', '-0.0788', '1.046', '0.2115', '0.1436', '0.2471', '-0.0719', '-0.1078', '0.2612', '0.724', '0.0185', '0.3196', '0.10486', '0.1192', '-0.2344', '0.681', '0.2673']",C61264,,D009087,,,10056892,
mondo:0009662,mucopolysaccharidosis type 7,"['MPS7', 'Beta-glucuronidase deficiency', 'MPS 7', 'MPS VII - Sly syndrome', 'MPSVII', 'mucopolysaccharidosis, type 7', 'MPS VII', 'Sly disease', 'mucopolysaccharidosis, type VII', 'Sly syndrome', 'deficiency of beta-glucuronidase', 'mucopolysaccharidosis VII', 'Gusb deficiency', 'mucopolysaccharidosis type VII', 'beta-glucuronidase deficiency']",12803,253220,584,C0085132,"['-0.4111', '0.2365', '0.03836', '0.1488', '-0.0677', '-0.9253', '0.3127', '0.653', '-0.3904', '-0.2922', '-0.4016', '-0.2203', '0.2014', '0.2239', '-0.1521', '-0.2201', '0.039', '-0.10834', '-0.6943', '-0.1671', '-0.2218', '0.02124', '0.999', '-0.533', '-0.2559', '-0.0167', '0.001446', '0.2595', '-0.381', '0.09515', '0.6978', '0.1744', '-0.00654', '0.4233', '-0.2427', '-0.6025', '-0.4053', '-0.31', '0.4749', '0.3782', '-0.4126', '-0.3325', '0.493', '0.595', '-0.1288', '0.02065', '0.07837', '-0.1611', '0.10254', '-0.523', '-0.09656', '-0.1854', '0.0608', '0.04187', '0.1919', '-0.8154', '-0.6475', '-0.4277', '0.4448', '-0.3262', '0.1427', '-0.2688', '-0.0751', '0.05853', '0.1516', '-0.1302', '0.327', '-0.422', '-0.5303', '0.3025', '-0.6963', '-0.2222', '0.0762', '0.01086', '0.1263', '0.186', '0.2408', '-0.01991', '-0.3271', '-0.376', '-0.3867', '-0.4124', '-0.438', '0.726', '-0.396', '0.7104', '0.05127', '0.278', '0.448', '0.1976', '0.06064', '0.02293', '-0.4048', '-0.00533', '0.4873', '0.6763', '0.5054', '-0.622', '0.634', '-0.02316']",C84903,,D016538,,,10056893,
mondo:0009663,mucus inspissation of respiratory tract,['mucus inspissation of respiratory tract'],,253240,,C1854729,,,,C565366,,,,
mondo:0009664,mulibrey nanism,"['Perheentupa syndrome', 'pericardial constriction and growth failure', 'mulibrey dwarfism', 'pericardial constriction and Growth failure', 'mulibrey nanism', 'MUL', 'muscle-liver-brain-eye nanism', 'pericardial constriction-growth failure syndrome']",0050436,253250,2576,C2931895,"['-0.0887', '-0.1124', '0.1183', '-0.2168', '0.081', '-0.2551', '-0.2666', '0.8022', '-0.1251', '-0.1445', '-0.693', '0.3057', '0.3525', '0.04166', '-0.649', '0.04422', '0.2937', '-0.06635', '-0.1927', '-0.684', '0.03308', '-0.3108', '0.7373', '-0.372', '-0.4329', '-0.3516', '0.1396', '-0.4097', '0.2966', '-0.3357', '0.7266', '-0.00164', '0.6235', '-0.6885', '-0.1744', '0.644', '-0.06824', '0.1313', '-0.06555', '-0.10974', '-0.1611', '-0.1737', '0.1833', '0.2178', '-0.2133', '-0.2769', '0.2566', '0.0904', '-0.4634', '0.05728', '-0.1674', '0.634', '-0.6406', '0.1667', '-0.01796', '0.0313', '0.1566', '-0.2343', '0.0734', '-0.0632', '-0.0691', '0.2651', '-0.4062', '0.2407', '-0.2303', '0.02982', '-0.1423', '0.9595', '-0.589', '0.5273', '0.0692', '0.6533', '0.02202', '0.745', '-0.64', '0.0978', '0.0925', '0.0949', '-0.02177', '-0.1887', '0.0798', '0.2289', '-0.608', '0.00512', '-0.615', '0.4895', '0.5483', '-0.3652', '0.287', '0.1533', '-0.03625', '-0.002855', '-0.1449', '0.1653', '0.8013', '-0.1343', '0.6353', '-0.1021', '0.02074', '-0.1455']",C84906,,D050336,759.89,,,
mondo:0009665,biotinidase deficiency,"['biotin deficiency', 'juvenile-onset multiple carboxylase deficiency', 'late-onset multiple carboxylase deficiency', 'late-onset biotin-responsive multiple carboxylase deficiency', 'multiple carboxylase deficiency, juvenile-onset', 'multiple carboxylase deficiency, late-onset', 'deficiency of biotinidase', 'biotinidase deficiency', 'BTD deficiency']",856,253260,79241,CN043572,"['0.02466', '0.553', '-0.5566', '-0.2563', '0.1449', '-0.468', '-0.2357', '1.145', '-0.1772', '0.5117', '0.0791', '0.0003765', '0.1875', '0.012825', '0.01181', '-0.2393', '0.1256', '-0.3384', '-0.5205', '-1.126', '0.298', '-0.5903', '0.1674', '0.3457', '-0.195', '-0.175', '-0.953', '-0.1011', '-0.371', '0.00678', '0.01473', '-0.3328', '0.10474', '0.1982', '-0.6', '-0.2026', '-0.6963', '-0.4805', '-0.3384', '0.785', '0.691', '-0.4133', '0.504', '-0.11804', '0.1329', '-0.397', '0.007595', '-0.6455', '-0.2256', '0.296', '-0.534', '0.04153', '-0.11066', '-0.1083', '-0.2544', '0.1544', '0.5327', '-0.6855', '-0.167', '0.03296', '0.129', '0.313', '0.2783', '-0.02495', '0.3752', '0.662', '0.1781', '0.4353', '0.11066', '0.7227', '0.1696', '-0.2556', '-0.07556', '-0.7583', '-0.00799', '-0.1294', '0.149', '-0.2494', '0.1443', '0.556', '0.6167', '-0.2275', '0.1404', '0.2264', '0.1329', '0.2449', '-0.1027', '-0.03099', '0.1835', '0.7266', '0.9087', '0.6', '0.0938', '-0.0809', '-0.02296', '1.051', '0.1813', '-0.1332', '0.1125', '-0.01283']",C84598,,D028921,277.6,D81.810,10071434,
mondo:0009666,holocarboxylase synthetase deficiency,"['holocarboxylase synthetase deficiency', 'multiple carboxylase deficiency', 'multiple carboxylase deficiency, neonatal form', 'HLCS deficiency', 'multiple carboxylase deficiency - neonatal onset', 'early-onset multiple carboxylase deficiency', 'holocarboxylase synthase deficiency', 'neonatal multiple carboxylase deficiency', 'multiple carboxylase deficiency, early onset', 'biotin-(propionyl-CoA-carboxylase) ligase deficiency']",859,253270,79242,C0268581,"['0.07367', '0.3894', '-0.53', '0.267', '0.0701', '-0.5664', '-0.3228', '0.3489', '-0.235', '-0.0007353', '-0.0797', '-0.1803', '0.01883', '0.3228', '-0.2737', '-0.0649', '-0.1005', '-0.229', '-0.579', '-1.426', '-0.1812', '-0.2715', '0.5527', '-0.438', '0.1544', '-0.3955', '-0.1683', '-0.10046', '-0.2998', '-0.0342', '0.0442', '-0.0319', '0.12256', '0.453', '-0.633', '0.3628', '-0.2834', '-0.5757', '0.01694', '0.3247', '0.3054', '-0.0822', '0.1288', '-0.02446', '-0.0683', '-0.06903', '-0.0824', '-0.524', '-0.1321', '0.532', '-0.4958', '-0.1938', '0.29', '-0.4487', '0.1307', '0.1', '0.4417', '0.4849', '-0.519', '-0.14', '0.2998', '0.2325', '0.694', '-0.4714', '-0.0206', '0.1287', '0.601', '-0.2084', '-0.3604', '0.512', '-0.405', '0.1027', '-0.3064', '-0.575', '-0.225', '0.2391', '0.09094', '-0.2786', '-0.02374', '0.10175', '0.4915', '0.07196', '-0.4136', '-0.1547', '0.741', '0.4182', '-0.1587', '-0.369', '0.3174', '0.8643', '0.3435', '0.175', '-0.0734', '-0.2783', '-0.0944', '0.9575', '0.1747', '-0.4343', '0.671', '-0.0417']",C98842,,D028922,270.8,,,
mondo:0009667,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A3","['Walker-Warburg syndrome or muscle-eye-brain disease, POMGNT1-related', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 3', 'muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 3', 'muscle-eye-brain-POMGNT1 related', 'MDDGA3']",0111236,253280,899,C3151519,,C126740,,,,,,
mondo:0009668,lethal multiple pterygium syndrome,"['lethal multiple pterygium syndrome', 'multiple pterygium syndrome lethal type', 'pterygium syndrome, multiple, lethal type', 'pterygium syndrome multiple lethal type', 'multiple pterygium syndrome, lethal type', 'LMPS', 'autosomal recessive lethal multiple pterygium syndrome']",,253290,33108,C1854678,"['-0.4', '0.506', '0.264', '-0.679', '0.283', '-0.256', '-0.1927', '0.7485', '-0.847', '-0.5195', '-0.1081', '0.3032', '-0.5317', '-0.2964', '-0.4697', '-0.2222', '0.146', '-0.08325', '0.1832', '-0.5586', '-0.544', '0.2177', '0.2072', '-0.536', '-0.2458', '0.2756', '-0.02905', '0.3591', '0.8', '-0.742', '0.3604', '-0.6323', '0.752', '0.1301', '0.33', '-0.10504', '-0.1589', '0.2247', '-0.1221', '0.1012', '-0.5166', '0.3323', '0.04834', '0.04694', '0.1406', '0.0907', '-0.0843', '0.597', '0.04376', '0.215', '-0.0591', '-0.4229', '0.2352', '0.1732', '-0.6', '-0.3545', '0.263', '-0.1102', '0.526', '0.1228', '0.0605', '-0.215', '-0.4119', '0.4895', '-0.4585', '-0.2788', '0.4292', '0.3198', '-0.4465', '0.2074', '0.2573', '0.1967', '-0.1103', '0.1926', '-0.3813', '0.696', '0.2368', '0.1174', '-0.627', '0.0947', '-0.2258', '0.6094', '0.6567', '0.4062', '0.354', '0.00821', '0.406', '0.01396', '-0.3079', '-0.1329', '0.321', '0.3225', '0.5425', '-0.1862', '1.005', '0.2422', '0.48', '-0.01721', '0.554', '0.2162']",C101038,,,759.89,,,
mondo:0009669,"spinal muscular atrophy, type 1","['severe infantile spinal muscular atrophy', 'spinal muscular atrophy-1', 'SMA, infantile acute form', 'SMA1', 'spinal muscular atrophy 1', 'SMA-I', 'Werdnig-Hoffmann disease', 'proximal spinal muscular atrophy, type 1', 'survival motor neuron spinal muscular atrophy', 'HMN (hereditary motor neuropathy) proximal type I', 'infantile spinal muscular atrophy', 'progressive muscular atrophy of infancy', 'hereditary motor neuropathy proximal type I', 'infantile muscular atrophy', 'spinal muscular atrophies of childhood', 'muscular atrophy, infantile', 'spinal muscular atrophy, type I', 'proximal spinal muscular atrophy type 1', 'Werdnig Hoffmann disease', 'SMA type 1', 'SMA type I', 'Werdnig-Hoffman disease']",13137,253300,83330,,"['-0.02348', '0.0359', '-0.01159', '-0.00795', '0.01825', '-0.05267', '0.01607', '0.05405', '-0.0438', '-0.01706', '-0.007153', '-0.006794', '-0.02837', '0.02907', '0.005756', '-0.01196', '0.006405', '-0.01733', '-0.02327', '-0.0713', '0.02365', '-0.02538', '0.0337', '-0.006683', '0.00169', '-0.008446', '-0.02077', '0.002071', '0.0112', '-0.01773', '0.03775', '0.00509', '0.03494', '0.01643', '0.02377', '-0.02502', '-0.01631', '-0.01634', '0.01442', '-0.02525', '-0.01155', '-0.01627', '0.01616', '-0.00895', '0.01027', '-0.02643', '-0.002432', '0.01364', '0.01268', '0.012695', '0.00417', '0.000576', '0.01639', '0.002064', '-0.000729', '-0.01852', '0.01988', '-0.01086', '-0.03357', '-0.00288', '0.02031', '0.00779', '0.001769', '-0.00536', '-0.005283', '0.0225', '0.02824', '0.02101', '-0.03882', '0.04468', '-0.03748', '-0.0004113', '0.01675', '-0.02937', '0.02559', '0.01523', '0.006718', '0.01098', '-0.0254', '-0.02309', '-0.003542', '-0.01886', '-0.002022', '0.03046', '-0.001457', '-0.01707', '0.01131', '0.04596', '0.04935', '0.01721', '0.009155', '0.02463', '0.010086', '0.02911', '0.07733', '0.03607', '0.02992', '-0.04883', '-0.00948', '0.01041']",C98670,,,335.11,,,
mondo:0009670,lethal congenital contracture syndrome 1,"['Lccs', 'lethal congenital contracture syndrome caused by mutation in GLE1', 'lethal autosomal recessive syndrome of multiple congenital contractures', 'lethal congenital contracture syndrome 1', 'lethal congenital contracture syndrome type 1', 'Herva disease', 'GLE1 lethal congenital contracture syndrome', 'multiple contracture syndrome, Finnish type', 'LCCS1']",0060559,253310,1486,C1854664,"['-0.3875', '0.003725', '0.04126', '-0.1595', '0.1165', '-0.578', '0.04028', '0.4504', '-0.8413', '-0.281', '-0.3445', '-0.00487', '0.0794', '0.01362', '0.1013', '-0.0911', '0.1327', '-0.0347', '-0.09174', '-0.5737', '-0.0346', '-0.3164', '0.7754', '-0.4873', '0.08997', '0.1683', '0.01307', '0.337', '0.0506', '-0.2004', '-0.004467', '-0.007263', '0.0928', '0.3135', '-0.004158', '-0.02449', '-0.02274', '0.06946', '0.316', '-0.0177', '-0.0345', '-0.3145', '0.1179', '0.3425', '0.0909', '0.0115', '-0.1407', '0.286', '0.2455', '-0.1066', '-0.3445', '-0.3237', '0.1511', '-0.1805', '-0.2225', '-0.4014', '0.2234', '-0.2406', '0.07837', '-0.0316', '0.04178', '-0.2079', '-0.1581', '0.2024', '-0.3105', '-0.283', '0.4731', '0.2338', '-0.3115', '0.1565', '0.010704', '0.3955', '0.163', '-0.2673', '-0.1785', '-0.0514', '0.0865', '0.01096', '-0.7524', '-0.05585', '-0.2325', '0.1436', '0.3809', '0.4758', '-0.2612', '0.2803', '0.2473', '0.4297', '-0.06555', '-0.3306', '0.3208', '0.3962', '0.2192', '-0.02283', '0.0827', '-0.04517', '0.8096', '-0.4243', '0.3787', '0.1047']",,,C537194,,,,
mondo:0009671,intellectual disability-myopathy-short stature-endocrine defect syndrome,"['Chudley-Rozdilsky syndrome', 'Chudley Rozdilsky syndrome', 'Chudley syndrome', 'multicore myopathy with mental retardation, short stature, and hypogonadotropic hypogonadism', 'multicore myopathy with intellectual disability, short stature, and hypogonadotropic hypogonadism']",,253320,3068,C1854663,,,,C535458,,,,
mondo:0009672,"spinal muscular atrophy, type III","['juvenile spinal muscular atrophy', 'Sma 3', 'SMA type 3', 'SMA-III', 'spinal muscular atrophy, type 3', 'paediatric spinal muscular atrophy', 'type III spinal muscular atrophy', 'SMA type III', 'KWS', 'spinal muscular atrophy III', 'spinal muscular atrophy, mild childhood and adolescent form', 'Kugelberg-Welander syndrome', 'pediatric spinal muscular atrophy', 'SMA 3', 'spinal muscular atrophy type 3', 'spinal muscular atrophy, type III', 'spinal muscular atrophy-3', 'spinal muscular atrophy, familial', 'proximal spinal muscular atrophy type 3', 'muscular atrophy, juvenile', 'childhood spinal muscular atrophy', 'spinal muscular atrophy of childhood', 'spinal muscular atrophy, type III, modifier of', 'Kugelberg-Welander disease', 'SMA3']",12376,253400,83419,C0700595,"['-0.12494', '0.0733', '0.07324', '-0.02686', '-0.01799', '-0.4863', '0.4417', '1.293', '-1.503', '-0.1373', '-0.629', '0.474', '-0.4727', '0.2437', '0.9097', '-0.2495', '-0.4543', '-0.5957', '-0.1382', '-0.1233', '-0.309', '-0.954', '0.502', '0.08453', '-0.02934', '-0.4346', '0.0625', '0.2493', '-1.36', '-0.02312', '0.5957', '0.5547', '0.04456', '-0.2107', '-0.2795', '-0.2318', '-0.003859', '-0.0361', '0.07806', '-0.1439', '-0.06494', '-0.2559', '-0.2076', '0.3484', '0.2461', '-0.2617', '-0.532', '0.03387', '-0.1959', '0.215', '-0.3352', '-0.458', '-0.5977', '-0.5864', '-0.3162', '-0.533', '-0.1644', '0.0394', '-0.2235', '0.03873', '-0.06183', '0.3125', '0.2147', '0.2257', '-0.499', '0.1816', '-0.03317', '0.1688', '-0.4316', '-0.1175', '0.1085', '0.1056', '0.3096', '-0.3552', '1.151', '0.3965', '-0.2693', '-0.02249', '-0.56', '-0.1804', '0.5376', '-0.298', '0.3154', '0.523', '-0.01585', '0.2642', '0.015594', '0.1007', '0.579', '-0.0674', '0.06946', '0.3145', '-0.5054', '0.3882', '0.1757', '-0.1147', '0.834', '-0.1888', '-0.2101', '0.007126']",C118847,,,335.11,,,
mondo:0009673,"spinal muscular atrophy, type II","['spinal muscular atrophy, type 2', 'SMA type II', 'spinal muscular atrophy type II', 'Dubowitz disease', 'SMA2', 'muscular atrophy, spinal, infantile chronic form', 'spinal muscular atrophy, type II', 'SMA II', 'chronic spinal muscular atrophy', 'spinal muscular atrophy type 2', 'muscular atrophy, spinal, intermediate type', 'chronic infantile spinal muscular atrophy', 'Sma 2', 'SMA-II', 'Intermediate spinal muscular atrophy', 'proximal spinal muscular atrophy type 2', 'SMA type 2', 'muscular atrophy, spinal, Intermediate type', 'spinal muscular atrophy-2']",0050530,253550,83418,,"['0.2106', '-0.2006', '-0.4', '0.0738', '0.02849', '-0.5317', '0.3699', '1.11', '-1.146', '-0.3271', '-0.4377', '0.1549', '-0.3088', '0.08234', '0.4473', '-0.916', '-0.6807', '-0.3699', '-0.3647', '-0.6196', '0.11487', '-0.596', '0.469', '-0.0254', '0.191', '-0.2966', '-0.2238', '0.2969', '-0.866', '0.03455', '0.3008', '0.364', '-0.2386', '-0.3547', '-0.346', '-0.622', '-0.1782', '-0.172', '0.312', '-0.1774', '-0.4631', '-0.5454', '0.00775', '0.459', '0.03223', '0.0807', '-0.5024', '-0.07806', '0.2137', '-0.2025', '-0.324', '-0.8135', '-0.5605', '-0.1488', '-0.0484', '-0.4744', '-0.03824', '0.1514', '0.04437', '-0.013275', '0.1708', '0.494', '0.4092', '0.1475', '-0.608', '-0.3992', '0.1924', '0.1681', '-0.4956', '-0.11816', '0.0745', '-0.3286', '-0.04495', '-0.2715', '0.79', '0.5957', '-0.4326', '-0.2676', '-0.4783', '-0.36', '0.1312', '-0.596', '-0.2966', '0.7563', '-0.6416', '0.66', '-0.01263', '0.4473', '0.469', '0.09827', '-0.1481', '0.0904', '-0.723', '0.2197', '0.0107', '-0.0797', '0.7397', '-0.1517', '0.1718', '-0.3088']",,,C536879,335.19,,,
mondo:0009674,"muscular dystrophy, adult-onset, with leukoencephalopathy","['muscular dystrophy, adult-onset, with leukoencephalopathy']",,253590,,C1854646,,,,C565361,,,,
mondo:0009675,autosomal recessive limb-girdle muscular dystrophy type 2A,"['limb-girdle muscular dystrophy due to calpain deficiency', 'LGMD2A', 'limb-girdle muscular dystrophy type 2A', 'primary calpainopathy', 'limb-girdle muscular dystrophy type 2', 'myositis, eosinophilic', 'muscular dystrophy, Pelvofemoral', 'CAPN3 autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, limb-girdle, autosomal recessive 1', 'Leyden-Moebius muscular dystrophy', 'muscular dystrophy, limb-girdle, type 2', 'LGMD2', 'pelvofemoral muscular dystrophy', 'calpainopathy', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in CAPN3', 'muscular dystrophy limb girdle type 2A, erb type', 'muscular dystrophy, limb-girdle, type 2A']",0110275,253600,267,,"['-0.1266', '-0.6025', '-0.648', '-0.0832', '0.6006', '-1.255', '0.05978', '0.527', '-2.057', '-0.812', '0.2207', '0.4812', '-0.08826', '1.123', '0.0843', '0.3662', '-0.7695', '-0.6797', '-0.6064', '-0.732', '0.1383', '0.10504', '0.2725', '0.828', '0.0906', '0.1732', '0.03372', '-0.9053', '0.4482', '-0.284', '0.841', '0.06146', '0.666', '0.07904', '0.2742', '0.03009', '-0.711', '0.4438', '-0.184', '-0.403', '0.321', '-0.5225', '-0.289', '0.4866', '-0.1758', '0.2455', '-0.02374', '0.701', '-0.1389', '0.695', '0.2925', '-0.2795', '0.232', '-0.877', '0.06854', '-0.772', '0.4368', '0.8506', '-0.3757', '-0.2412', '0.4138', '0.06537', '-0.0695', '-0.03111', '-0.0552', '0.116', '0.14', '0.688', '-0.3323', '-0.06046', '-0.1415', '0.556', '0.2339', '0.11426', '0.709', '0.581', '0.0627', '0.403', '0.038', '0.0626', '-0.2056', '-0.01254', '0.09216', '0.3625', '-0.1469', '0.359', '-0.3213', '-0.531', '0.9214', '0.10046', '-0.1605', '0.1445', '0.378', '0.9395', '0.143', '-0.0728', '0.2751', '-0.3958', '0.00964', '0.04166']",C142079,,C535895,,,,
mondo:0009676,autosomal recessive limb-girdle muscular dystrophy type 2B,"['limb-girdle muscular dystrophy type 2B', 'limb-girdle muscular dystrophy, type 2B', 'muscular dystrophy, limb-girdle, type 2B', 'DYSF autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, limb-girdle, type 3', 'limb-girdle muscular dystrophy due to dysferlin deficiency', 'limb-girdle muscular dystrophy type 3', 'LGMD2B', 'muscular dystrophy, limb-girdle, autosomal recessive 2', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in DYSF', 'LGMD3']",0110276,253601,268,,"['-0.2517', '-0.576', '-0.596', '-0.426', '0.4731', '-1.306', '0.2286', '0.8174', '-2.08', '-0.973', '0.0642', '0.699', '-0.3738', '0.9287', '-0.03076', '0.597', '-0.956', '-0.533', '-0.65', '-0.813', '0.164', '-0.083', '0.3684', '0.591', '0.3696', '0.1475', '-0.05533', '-1.07', '0.2869', '-0.603', '0.926', '-0.1027', '0.5845', '0.1522', '-0.02155', '-0.0716', '-0.584', '0.4634', '0.2983', '-0.3557', '0.05737', '-0.434', '-0.247', '0.4739', '-0.519', '0.2281', '0.05267', '0.683', '-0.2957', '0.517', '0.5513', '-0.4138', '0.4307', '-0.8325', '0.12103', '-0.5566', '0.526', '0.716', '-0.3445', '0.1252', '0.2632', '-0.02718', '-0.10236', '-0.1267', '-0.12476', '0.04514', '0.2214', '0.486', '-0.3147', '-0.2295', '-0.2316', '0.4175', '0.306', '-0.02014', '0.6406', '0.5703', '-0.1698', '0.2673', '0.1299', '0.045', '-0.0554', '0.1538', '-0.0629', '-0.01165', '-0.1041', '0.2913', '-0.1504', '-0.419', '0.9443', '0.4177', '-0.2458', '0.06995', '0.585', '0.891', '-0.2166', '0.02591', '0.2778', '-0.3884', '-0.2761', '-0.1103']",C142080,,C535899,,,,
mondo:0009677,autosomal recessive limb-girdle muscular dystrophy type 2C,"['deficiency of sarcoglycan gamma', 'autosomal recessive Duchenne-like muscular dystrophy type 1', 'gamma-sarcoglycanopathy', 'Adhalin deficiency, secondary', 'limb-girdle muscular dystrophy, type 2C', 'limb-girdle muscular dystrophy with gamma-sarcoglycan deficiency', 'muscular dystrophy, Duchenne-like', 'severe childhood autosomal recessive muscular dystrophy North African type', 'Maghrebian myopathy', 'DMDA1', 'muscular dystrophy, limb-girdle, autosomal recessive 5', 'Dmda', 'severe childhood autosomal recessive muscular dystrophy, North African type', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in SGCG', 'sarcoglycan, gamma, deficiency of', 'Duchenne-like muscular dystrophy, autosomal recessive, type 1', 'LGMD2C', 'SGCG autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, limb-girdle, type 2C', 'SCARMD', 'limb-girdle muscular dystrophy due to gamma-sarcoglycan deficiency']",0110277,253700,353,C0410173,"['-0.2017', '-0.6924', '-0.6675', '-0.443', '0.607', '-1.19', '0.2664', '0.785', '-1.797', '-0.8994', '-0.0799', '0.4153', '-0.1576', '0.7217', '0.2493', '0.4165', '-0.9243', '-0.3884', '-0.6597', '-0.69', '0.010414', '0.05603', '0.0888', '0.715', '0.2296', '-0.01273', '-0.0012665', '-1.113', '0.2007', '-0.698', '0.7056', '0.0587', '0.707', '0.2059', '-0.02727', '-0.1638', '-0.6475', '0.4912', '0.01165', '-0.4224', '0.1305', '-0.3774', '-0.506', '0.1431', '-0.3552', '0.1895', '-0.03763', '0.7397', '-0.2472', '0.6694', '0.3303', '-0.3032', '0.2957', '-1.145', '0.1907', '-0.4646', '0.3435', '0.9146', '-0.3367', '0.12054', '0.2415', '0.0678', '-0.1771', '-0.005676', '-0.0121', '0.0236', '-0.2058', '0.4397', '-0.5415', '-0.3508', '-0.1186', '0.5723', '0.2031', '0.05597', '0.8066', '0.757', '0.227', '0.3088', '0.2737', '0.2413', '-0.122', '0.1823', '0.2212', '-0.08026', '-0.3738', '0.2349', '-0.0886', '-0.1587', '0.825', '0.294', '-0.2888', '0.3333', '0.2722', '0.9136', '-0.2185', '0.1549', '0.5894', '-0.4966', '-0.29', '-0.1482']",,,C535900,,,,
mondo:0009678,"muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4","['muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A, 4', 'muscle-eye-brain-FKTN related', 'Fukuyama congenital muscular dystrophy', 'congenital muscular dystrophy, Fukuyama type', 'FCMD', 'MDDGA4', 'muscular dystrophy-dystroglycanopathy (congenital with Brain and eye anomalies) type A, 4', 'Walker-Warburg syndrome or muscle-eye-brain disease, FKTN-related']",0050559,253800,899,C0410174,"['0.3923', '-0.447', '-0.7217', '-0.0731', '0.6714', '-0.9814', '0.446', '0.9307', '-1.517', '-0.7275', '-0.1251', '0.1823', '-0.2166', '0.771', '0.108', '0.3206', '-0.5503', '-0.4707', '-0.4119', '-0.7314', '-0.0986', '0.2666', '0.317', '0.8237', '0.1305', '-0.4119', '0.0856', '-0.768', '0.1222', '-0.3206', '0.7705', '-0.07086', '0.4963', '0.2057', '0.326', '0.2158', '-0.365', '0.01492', '-0.1089', '0.00951', '-0.04123', '-0.2805', '-0.46', '0.1678', '-0.002571', '0.601', '-0.1892', '0.432', '-0.359', '0.505', '0.02208', '-0.0223', '0.4055', '-0.845', '-0.1425', '-0.492', '0.3713', '0.8706', '-0.31', '-0.05942', '0.06464', '0.05563', '-0.01267', '0.1556', '0.1342', '-0.1523', '-0.02173', '0.1965', '-0.544', '-0.1722', '-0.03253', '0.559', '-0.05386', '-0.2722', '0.55', '0.4177', '0.114', '0.01997', '-0.0704', '-0.00942', '0.3052', '-0.2332', '-0.3647', '0.2786', '0.1324', '0.08496', '-0.1482', '0.084', '0.7837', '0.2094', '-0.5776', '0.11554', '0.415', '0.6787', '-0.3032', '0.0402', '0.2155', '-0.4373', '0.363', '0.263']",C126741,,,,,,
mondo:0009679,arthrogryposis due to muscular dystrophy,"['muscular dystrophy, congenital, producing arthrogryposis', 'congenital muscular dystrophy producing arthrogryposis']",0110631,253900,1155,C1850865,,,,C564985,,,,
mondo:0009680,congenital muscular dystrophy-infantile cataract-hypogonadism syndrome,"['familial congenital muscular dystrophy with gonadal dysgenesis', 'muscular dystrophy, congenital, with infantile cataract and hypogonadism', 'Bassoe syndrome', 'benign muscular dystrophy with hypergonadotrophic hypogonadism and congenital cataract', 'muscular dystrophy, congenital, infantile with cataract and hypogonadism']",,254000,1875,C2931578,,,,,,,,
mondo:0009681,Ullrich congenital muscular dystrophy 1,"['Ullrich disease', 'muscular dystrophy, Scleroatonic', 'Ullrich congenital muscular dystrophy type 1', 'UCMD1', 'Ullrich congenital muscular dystrophy 1', 'Ullrich Scleroatonic muscular dystrophy', 'Ullrich congenital muscular dystrophy']",,254090,,CN033863,,,,,,,,
mondo:0009682,"muscular dystrophy, congenital, with rapid progression","['muscular dystrophy, congenital, with rapid progression']",,254100,,C1850840,,,,C564983,,,,
mondo:0009683,autosomal recessive limb-girdle muscular dystrophy type 2H,"['TRIM32 autosomal recessive limb-girdle muscular dystrophy', 'muscular dystrophy, Hutterite type', 'LGMD2H', 'muscular dystrophy, limb-girdle, autosomal recessive 8', 'muscular dystrophy limb-girdle type 2H', 'Sarcotubular myopathy', 'autosomal recessive limb-girdle muscular dystrophy caused by mutation in TRIM32', 'muscular dystrophy Hutterite type', 'limb-girdle muscular dystrophy type 2H', 'sarcotubular myopathy', 'muscular dystrophy, limb-girdle, type 2H', 'limb-girdle muscular dystrophy due to TRIM32 deficiency']",0110282,254110,1878,C0270968,"['-0.3613', '-0.8066', '-0.6406', '-0.3198', '0.4207', '-1.396', '0.11664', '0.6064', '-1.896', '-0.9136', '-0.00925', '0.5605', '-0.04904', '1.062', '0.3643', '0.2045', '-0.6562', '-0.6323', '-0.4404', '-0.8813', '0.04172', '0.01573', '0.3691', '0.797', '0.2437', '0.11566', '-0.1383', '-0.765', '0.2607', '-0.521', '0.647', '0.02402', '0.5156', '0.2659', '0.3875', '0.1343', '-0.7075', '0.3687', '-0.1049', '-0.4739', '0.263', '-0.1683', '-0.2595', '0.5327', '0.09937', '0.4333', '0.1245', '0.495', '-0.3384', '0.583', '0.4438', '-0.364', '0.3408', '-0.8047', '0.1519', '-0.804', '0.3665', '1.06', '-0.1178', '-0.0002', '0.356', '0.03357', '-0.04422', '-0.1011', '0.0998', '0.2091', '0.3955', '0.563', '-0.2068', '-0.10236', '-0.01881', '0.2717', '0.3237', '-0.2576', '0.7246', '0.5566', '-0.07605', '0.2448', '-0.11884', '0.07263', '0.2979', '0.07074', '0.004074', '0.289', '-0.2062', '0.2827', '-0.04468', '-0.4497', '0.847', '0.1295', '-0.265', '0.2382', '0.4612', '0.944', '0.08203', '0.01076', '0.4006', '-0.5977', '0.03046', '0.02126']",,,C535897,359.89,,,
mondo:0009684,"muscular hypertonia, lethal","['muscular hypertonia, lethal']",,254120,,C1850827,,,,C564982,,,,
mondo:0009685,Miyoshi myopathy,"['MMD1', 'Miyoshi muscular dystrophy type 1', 'Miyoshi muscular dystrophy', 'MM', 'Miyoshi muscular dystrophy 1', 'muscular dystrophy, distal, late onset, autosomal recessive', 'Miyoshi distal myopathy']",0070198,,45448,,"['-0.5674', '-0.3076', '-0.468', '-0.3208', '0.02292', '-0.7627', '-0.0775', '1.384', '-1.068', '-0.3606', '-0.004406', '0.3037', '0.1515', '0.2301', '0.483', '-0.1678', '-0.2966', '-0.0465', '-0.456', '-0.468', '0.1268', '-0.05405', '0.1652', '0.0841', '0.084', '-0.152', '-0.4438', '0.1835', '-0.4182', '-0.1991', '0.38', '-0.1536', '-0.1753', '-0.3198', '0.2534', '-0.3972', '-0.06506', '-0.475', '0.4392', '-0.033', '-0.03044', '-0.983', '0.0871', '0.7046', '0.1696', '-0.03043', '-0.6426', '-0.10126', '0.2002', '0.2269', '-0.1805', '0.10297', '-0.0751', '-0.4797', '0.4028', '-0.398', '0.5527', '0.0319', '-0.05725', '-0.4832', '0.0561', '0.745', '-0.352', '-0.4182', '-0.3335', '0.4377', '-0.1886', '0.357', '-0.3662', '0.09265', '-0.01142', '-0.3196', '0.1173', '0.692', '0.8022', '0.333', '-0.2175', '-0.171', '-0.0741', '-0.4436', '-0.0695', '-0.3552', '0.789', '0.8647', '0.013145', '0.7183', '-0.4539', '0.1964', '0.04855', '-0.328', '-0.2556', '-0.3462', '0.03302', '0.3118', '0.747', '-0.2438', '0.674', '-0.4062', '-0.6147', '-0.0758']",C118846,,C537480,,,,
mondo:0009686,"musk, inability to smell","['musk, inability to smell']",,254150,,C1850807,,,,C564980,,,,
mondo:0009687,"myasthenia, congenital, refractory to acetylcholinesterase inhibitors","['myasthenia, congenital, refractory to acetylcholinesterase inhibitors']",,254190,,C1850806,,,,C564979,,,,
mondo:0009688,myasthenia gravis,"['MG', 'myasthenia gravis', 'acquired myasthenia', 'autoimmune myasthenia gravis']",437,254200,589,C0026896,"['-0.0632', '0.6445', '-0.2559', '0.108', '-0.1559', '-0.0957', '0.3176', '0.1799', '-0.799', '-0.516', '0.248', '-0.2004', '0.2607', '0.617', '-0.149', '0.0582', '-0.5005', '-0.519', '-0.7183', '-0.3674', '0.1995', '0.244', '0.02672', '0.3877', '-0.6445', '-0.685', '-0.453', '-0.146', '0.303', '-0.033', '0.2852', '0.3142', '0.4927', '-0.2373', '0.2146', '0.3914', '0.16', '0.05945', '0.0293', '0.2461', '0.2439', '-0.2358', '-0.4692', '-0.2457', '0.4236', '-0.2527', '-0.03894', '0.002651', '0.435', '0.505', '-0.4993', '0.2013', '0.1606', '-0.619', '-0.012535', '0.3171', '0.06274', '0.4382', '-0.1898', '-0.11865', '0.3325', '0.1512', '-0.4604', '0.4055', '-0.2712', '-0.05765', '0.03784', '0.4148', '-0.232', '0.4849', '0.5537', '-0.4753', '0.608', '-0.2234', '0.6978', '0.743', '-0.11053', '0.9106', '-0.11774', '0.2181', '-0.09576', '0.3083', '0.671', '-0.562', '-0.1197', '0.2664', '-0.0663', '-0.067', '1.353', '0.4', '-0.06287', '-0.265', '0.03955', '0.347', '0.937', '0.1022', '-0.3596', '0.1425', '-0.067', '0.3545']",C60989,0004991,D009157,358.00,G70.0,10028417,
mondo:0009689,congenital myasthenic syndrome 6,"['myasthenia gravis familial infantile 2 (formerly)', 'CMSEA', 'congenital myasthenic syndrome type Ia2, formerly', 'myasthenia gravis, familial infantile, 2, formerly', 'familial infantile myasthenia', 'CMS1A', 'congenital myasthenic syndrome type 6', 'myasthenic syndrome congenital associated with episodic apnea', 'Cms Ia2, formerly', 'congenital myasthenic syndrome with episodic apnea', 'CHAT congenital myasthenic syndrome', 'myasthenic syndrome, presynaptic, congenital, associated with episodic apnea', 'myasthenic syndrome, congenital, 6, presynaptic', 'FIM', 'myasthenia, familial infantile, formerly', 'myasthenic syndrome, congenital, associated with episodic apnea', 'Cms Ia2', 'congenital myasthenic syndrome caused by mutation in CHAT', 'CMS6', 'congenital presynaptic myasthenic syndrome associated with episodic apnea', 'FIMG2', 'familial infantile myasthenia gravis 2', 'CMS-ea', 'congenital myasthenic syndrome type Ia2', 'CMS1A2, formerly', 'CMS1A2', 'CMS Ia2, formerly', 'myasthenia familial infantile', 'CMS w/episodic apnea', 'FIMG2 (formerly)', 'FIM, formerly', 'myasthenia gravis, familial infantile, 2', 'FIMG2, formerly', 'congenital myasthenic syndrome type Ia', 'congenital myasthenic syndrome 6, presynaptic', 'presynaptic congenital myasthenic syndrome 6', 'CMS Ia2', 'myasthenia, familial infantile', 'congenital myasthenic syndrome type 1a']",0110671,254210,,C0393929,,C132292,,C535759,358.00,,,
mondo:0009690,congenital myasthenic syndrome 10,"['congenital myasthenic syndrome type 10', 'muscular dystrophy, congenital, merosin-POSITIVE', 'CMS1B', 'myasthenia, limb-girdle, familial', 'DOK7 congenital myasthenic syndrome', 'Cms Ib', 'congenital myasthenic syndrome type IB, formerly', 'familial limb-girdle myasthenia', 'myasthenic myopathy, formerly', 'congenital muscular dystrophy merosin-positive', 'LGM', 'myasthenic syndrome, congenital, type 10', 'congenital myasthenic syndrome type IB', 'Cms Ib, formerly', 'congenital myasthenic syndrome caused by mutation in DOK7', 'myasthenic myopathy', 'myasthenia, limb-girdle, familial, formerly', 'CMS Ib', 'CMS10', 'myasthenic syndrome, congenital, 10']",0110668,609456,,C1836133,,,,C563716,358.00,,,
mondo:0009691,mycosis fungoides,"['CTCL/ mycosis fungoides', 'mycosis fungoides lymphoma', 'granuloma fungoides', 'MF', 'cutaneous T-cell lymphoma/mycosis fungoides', 'mycosis fungoides, Alibert-Bazin type', 'mycosis fungoides of unspecified site', 'mycosis fungoides NOS (morphologic abnormality)', 'mycosis fungoides, unspecified site, extranodal and solid organ sites', 'Alibert-Bazin syndrome', 'classic mycosis fungoides', 'mycosis fungoides', 'mycosis fungoides (morphologic abnormality)']",8691,254400,2584,C0026948,,C3246,1001051,D009182,202.1,C84.0,10028483,
mondo:0009692,primary myelofibrosis,"['Agnogenic myeloid metaplasia', 'idiopathic bone marrow fibrosis', 'idiopathic myelofibrosis', 'osteomyelofibrosis', 'myeloid metaplasia', 'myelofibrosis, somatic', 'myelofibrosis with myeloid metaplasia', 'bone marrow fibrosis', 'megakaryocytic myelosclerosis', 'aleukemic myelosis', 'chronic idiopathic myelofibrosis', 'myelosclerosis with myeloid metaplasia', 'myelofibrosis', 'CIMF', 'myelosclerosis', 'primary myelofibrosis', 'myelofibrosis with myeloid metaplasia, somatic', 'AMM']",4971,254450,824,C2355576,"['-0.1809', '0.4097', '-0.5137', '-0.2625', '-0.1239', '0.277', '-0.2764', '1.247', '-0.3696', '-0.54', '-0.1296', '0.2238', '0.0683', '-0.02625', '-0.0611', '-0.1666', '-0.892', '-0.2273', '0.6284', '-0.7', '-0.1653', '-0.406', '0.656', '-0.499', '0.2389', '0.524', '0.2517', '0.1595', '-0.5215', '0.603', '0.4587', '-0.448', '0.656', '0.002834', '0.5347', '-0.05292', '-0.7754', '-0.0559', '0.548', '-0.412', '0.12427', '0.4578', '0.2065', '-0.03102', '-0.2386', '-0.09766', '-0.4148', '-0.5605', '0.2686', '-0.1971', '0.44', '0.1052', '0.594', '0.2456', '0.2177', '0.1128', '-0.402', '0.003315', '-0.422', '-0.3323', '-0.1904', '0.57', '0.1514', '-0.409', '-0.3071', '-0.06195', '0.1888', '0.1007', '-0.476', '0.9893', '-0.1906', '0.3325', '-0.2886', '-0.2559', '0.3743', '0.2983', '-0.2512', '0.1638', '0.975', '-0.4492', '-0.2106', '-0.4355', '0.4875', '-0.28', '-0.268', '0.006107', '0.7017', '0.4539', '0.3804', '-0.5234', '-0.2368', '-0.3076', '-0.7505', '-0.591', '0.501', '0.4824', '-0.001332', '-0.4988', '0.07153', '-0.07214']",C2862,0002430,D055728,289.83,,,
mondo:0009693,plasma cell myeloma,"['myeloma, multiple', 'Kahler^s disease', 'multiple myeloma/plasma cell myeloma', 'myeloma, plasma cell, malignant', 'plasma cell myeloma', 'Al amyloidosis', 'myeloma', 'amyloidosis, systemic', 'plasma cell myeloid neoplasm', 'multiple myeloma, resistance to, Somatic mutation', 'myeloma - multiple', 'myeloid neoplasm of plasma cell', 'medullary plasmacytoma', 'multiple myeloma, susceptibility to, Somatic mutation', 'Kahler disease', 'multiple myeloma', 'myelomatosis']",9538,254500,85443,C0268381,"['-0.529', '0.0657', '0.1309', '-0.0914', '0.0962', '0.11096', '0.04514', '0.467', '-0.04474', '0.1715', '0.08417', '0.004356', '0.1321', '-0.04178', '-0.3503', '-0.1533', '-0.2062', '-0.1404', '0.1115', '-0.3267', '0.1219', '-0.6216', '0.5977', '-0.1956', '0.4832', '-0.1589', '0.1066', '-0.0795', '-0.3042', '-0.265', '0.1919', '0.02222', '0.6704', '0.0512', '0.2092', '-0.3572', '-0.6133', '-0.1757', '-0.1604', '-0.4753', '0.0102', '-0.2827', '0.278', '-0.4414', '0.01974', '-0.217', '-0.2323', '0.02357', '0.2104', '0.0999', '0.184', '0.1919', '0.3745', '0.2585', '-0.1614', '-0.182', '-0.07874', '-0.1896', '-0.4084', '0.0336', '0.532', '-0.001852', '-0.3733', '-0.4595', '-0.03195', '-0.00155', '0.4292', '0.4414', '0.012474', '0.2192', '0.1293', '-0.1305', '-0.217', '0.0834', '0.04794', '0.03836', '0.1027', '0.1704', '0.1617', '-0.64', '-0.5615', '-0.08105', '-0.187', '-0.1466', '-0.754', '-0.1599', '0.4302', '0.1934', '0.3462', '0.01464', '0.2554', '0.05002', '-0.00614', '-0.3906', '0.5845', '0.4382', '0.3035', '-0.1826', '-0.1965', '0.0701']",C3242,0001378,D009101,203.0,C90.0,10028228,
mondo:0009694,myeloperoxidase deficiency,"['MPO deficiency', 'MPOD', 'myeloperoxidase deficiency']",,254600,2587,C0398595,"['-0.2925', '-0.0497', '-0.01979', '-0.1864', '-0.02628', '-0.094', '0.2096', '0.0896', '0.05362', '-0.004425', '-0.1329', '0.1036', '-0.0675', '0.06445', '-0.1495', '-0.1075', '0.0386', '0.1776', '-0.2028', '-0.4138', '0.04776', '-0.0788', '0.3599', '-0.06683', '-0.08026', '0.02434', '-0.03455', '-0.1261', '-0.0656', '-0.3823', '0.1941', '0.002506', '0.2144', '0.274', '0.10815', '-0.0783', '-0.0874', '-0.10394', '-0.2064', '-0.2339', '-0.01756', '-0.05795', '0.2445', '-0.02565', '-0.2764', '-0.09235', '-0.03207', '-0.03073', '0.1721', '0.4736', '0.05066', '-0.0476', '0.1837', '0.0352', '-0.2407', '-0.03625', '0.1603', '-0.4014', '-0.2275', '0.04605', '0.001807', '0.3118', '0.06976', '-0.11206', '0.10645', '0.1389', '0.1914', '0.193', '-0.1471', '0.1404', '0.002716', '-0.04843', '-0.03464', '-0.04257', '0.03818', '-0.03714', '0.413', '0.10834', '0.07074', '-0.014435', '-0.2145', '0.0727', '0.02666', '0.08716', '-0.0639', '-0.02927', '0.1705', '0.1467', '0.3186', '-0.08466', '0.2969', '0.1293', '-0.0957', '-0.1293', '0.4482', '0.1904', '0.1464', '-0.4832', '-0.1912', '-0.0716']",,,C562864,288.8,,,
mondo:0009695,"myeloproliferative disease, autosomal recessive","['myeloproliferative disease, autosomal recessive']",,254700,,C1850779,,,,C564977,,,,
mondo:0009696,juvenile myoclonic epilepsy,"['EJM', 'Janz syndrome', 'myoclonic epilepsy, juvenile, 1', 'petit mal, impulsive', 'juvenile myoclonus epilepsy', 'JME', 'myoclonic epilepsy, juvenile, susceptibility to, 1', 'myoclonic epilepsy, juvenile', 'epilepsy, myoclonic juvenile']",4890,606904,307,C0270853,"['0.97', '0.1272', '-0.2812', '-0.2517', '-0.2429', '-0.413', '0.7134', '0.3208', '-0.5933', '-0.378', '0.2344', '-0.1813', '-0.2935', '0.4373', '-0.1266', '0.03824', '-0.265', '-0.4153', '-0.4783', '-0.5825', '-0.3438', '0.568', '0.282', '-0.496', '-0.2705', '-0.02945', '0.0181', '-0.1146', '-0.4402', '0.349', '0.3447', '-0.6577', '0.3452', '0.1109', '0.811', '0.3655', '-0.1154', '-0.11505', '0.0949', '-0.3774', '-0.02455', '-0.3271', '-0.09406', '-0.3035', '-0.333', '-0.683', '-0.3428', '0.3145', '0.548', '0.794', '-0.1506', '0.1522', '0.03262', '-0.531', '0.2632', '-0.1102', '-0.1644', '-0.02881', '-0.1406', '0.1726', '-0.6733', '0.4343', '0.6787', '-0.3926', '-0.4338', '1.625', '0.2456', '0.05463', '-0.9985', '0.7266', '0.9497', '0.8433', '-0.01173', '-0.3633', '0.1709', '0.809', '0.9355', '0.6284', '-0.4292', '0.2742', '-0.2742', '0.7476', '0.5015', '0.27', '0.4775', '0.2473', '0.1339', '0.6465', '0.807', '0.2566', '0.037', '0.01894', '-0.4563', '0.1444', '0.06854', '0.0991', '0.1926', '-0.629', '0.11053', '0.3103']",C84796,0006572,D020190,345.10,,10071082,
mondo:0009697,Lafora disease,"['myoclonic epilepsy of Lafora', 'epilepsy, progressive myoclonic 2A (Lafora)', 'Lafora progressive myoclonic epilepsy', 'Lafora disease', 'Lafora body disorder', 'epilepsy, progressive myoclonic, 2A', 'epilepsy, progressive myoclonic, 2B', 'Lafora^s disease', 'epilepsy progressive myoclonic 2', 'PME type 2', 'progressive myoclonic epilepsy type 2', 'epilepsy, progressive myoclonic 2B (Lafora)', 'Epm2', 'progressive myoclonus epilepsy type 2', 'Melf', 'EPM2', 'Lafora body disease']",3534,254780,501,C0751783,"['0.366', '0.7188', '-0.11176', '0.00889', '-0.6416', '-0.2006', '0.4111', '0.8174', '-0.4243', '0.11194', '-0.5063', '0.01622', '-0.2097', '-0.0967', '0.3965', '0.004135', '0.1342', '-0.1968', '-0.3105', '-0.7236', '-0.3706', '-0.1514', '0.3032', '0.6685', '-0.2177', '-0.2795', '-0.2883', '-0.6973', '-0.808', '-0.1744', '0.7705', '-0.0803', '0.2986', '0.0791', '0.258', '-0.013535', '-0.055', '-0.2986', '-0.2195', '0.165', '0.1465', '-0.53', '0.0622', '0.09625', '0.2869', '-0.3389', '-0.1967', '-0.8374', '0.2686', '0.656', '0.0937', '0.4172', '-0.01848', '-0.04855', '0.3281', '0.2144', '0.4583', '-0.2415', '-0.04218', '-0.273', '-0.2172', '0.1482', '0.3643', '-0.0333', '-0.3381', '0.4119', '0.589', '0.1617', '-0.3005', '0.0754', '0.00278', '-0.4255', '0.05066', '0.1371', '0.1344', '0.349', '0.6284', '-0.0187', '-0.557', '-0.45', '0.2058', '-0.1251', '-0.4226', '0.2034', '0.2267', '-0.2017', '-0.0394', '0.6', '0.3171', '0.2888', '0.2319', '-0.04755', '0.547', '-0.281', '0.308', '-0.1387', '0.5654', '-0.31', '0.4016', '0.128']",C84804,,D020192,,,10054030,
mondo:0009698,Unverricht-Lundborg syndrome,"['myoclonic epilepsy of Unverricht and Lundborg', 'progressive myoclonus epilepsy Baltic myoclonic epilepsy', 'Unverricht-Lundborg disease', 'ULD', 'epilepsy, progressive myoclonic, 1', 'PME type 1', 'epilepsy, progressive myoclonus 1', 'epilepsy, progressive myoclonic, 1A', 'Baltic myoclonic epilepsy', 'EPM1', 'epilepsy, progressive myoclonic type 1', 'progressive myoclonus epilepsy type 1', 'epilepsy, progressive myoclonic 1A (Unverricht and Lundborg)', 'progressive myoclonic epilepsy', 'progressive myoclonic epilepsy type 1', 'Unverricht - Lundborg disease', 'Unverricht^s disease', 'myoclonus progressive epilepsy of Unverricht and Lundborg', 'Uld']",3535,254800,308,C0751785,"['0.04178', '0.4438', '-0.3486', '-0.2411', '-0.3276', '-0.517', '0.445', '0.3494', '-0.565', '-0.1049', '-0.1632', '0.435', '-0.277', '-0.3198', '0.581', '-0.0707', '0.471', '-0.2261', '-0.02269', '-0.69', '0.04825', '0.2249', '0.003914', '-0.0647', '-0.0275', '-0.264', '-0.08075', '-0.5776', '-0.4216', '-0.02232', '0.2201', '0.1102', '0.06146', '-0.07074', '0.1743', '-0.01077', '-0.07446', '-0.404', '-0.3118', '-0.002523', '0.0832', '-0.5034', '-0.1251', '0.2141', '0.1123', '-0.3528', '-0.4348', '0.1698', '0.109', '0.3943', '-0.12085', '0.587', '-0.3628', '-0.1238', '0.231', '0.08453', '0.4692', '-0.1196', '-0.0987', '0.10895', '0.0581', '0.0009527', '0.3813', '0.02243', '-0.3457', '0.1309', '0.3616', '0.21', '-0.2307', '0.2053', '0.2756', '0.01828', '0.1416', '-0.1499', '0.07764', '0.2137', '0.366', '0.00479', '0.0713', '-0.1991', '-0.05258', '-0.1289', '-0.00344', '0.2644', '0.573', '-0.002163', '-0.007553', '0.4912', '0.4832', '0.357', '0.1423', '0.2336', '0.04495', '0.0815', '0.451', '0.2842', '0.401', '-0.0166', '-0.2734', '-0.10345']",,,D020194,,,10054895,
mondo:0009699,action myoclonus-renal failure syndrome,"['EPM4', 'progressive myoclonic epilepsy type 4', 'myoclonus-nephropathy syndrome', 'AMRF', 'action myoclonus-renal failure syndrome', 'epilepsy, progressive myoclonic 4, with or without renal failure', 'epilepsy, progressive myoclonic, 4, with or without renal failure']",0111444,254900,163696,,"['0.724', '0.1415', '-0.6733', '-0.1142', '-0.915', '-0.5293', '0.501', '0.4412', '-0.6504', '-0.2666', '0.0753', '-0.187', '0.2888', '0.1659', '0.4321', '-0.3677', '-0.3408', '-0.669', '-0.2603', '-1.339', '0.06247', '-0.7593', '-0.352', '0.09143', '0.4753', '-0.1152', '-0.214', '-0.2297', '0.0821', '0.3074', '0.171', '0.0763', '0.2036', '-0.447', '0.11273', '-0.2856', '-0.8057', '0.221', '-0.3594', '-0.1047', '-0.03748', '0.1388', '0.853', '0.0351', '0.2644', '-0.358', '-0.1449', '-0.55', '0.2147', '0.2883', '-0.0896', '0.611', '0.5503', '-0.1906', '0.1109', '-0.51', '0.0856', '-0.3215', '0.09076', '-0.1838', '0.0661', '-0.541', '0.431', '-0.7666', '-1.015', '0.2107', '0.6973', '0.489', '-0.5703', '-0.3015', '-0.893', '0.2957', '0.2695', '0.3667', '-0.0935', '0.3875', '0.3477', '0.02727', '0.1091', '0.2487', '-0.0719', '-0.287', '0.3296', '0.0991', '0.3323', '-0.282', '0.779', '0.0834', '0.77', '0.3914', '0.007515', '-0.2074', '0.1114', '0.3254', '0.2153', '0.2175', '0.0941', '-0.10425', '0.3254', '0.3494']",,,,,,,
mondo:0009701,"myopathy, granulovacuolar lobular, with electrical myotonia","['myopathy, granulovacuolar lobular, with electrical myotonia']",,254950,,C1850745,,,,C564974,,,,
mondo:0009702,myopathy due to malate-aspartate shuttle defect,['myopathy due to malate-aspartate shuttle defect'],,254960,,C1850744,,,,C564973,,,,
mondo:0009703,myopathy with abnormal lipid metabolism,"['LSMFLAD', 'lipid storage myopathy', 'myopathy with abnormal lipid metabolism', 'lipid storage myopathy due to flavin adenine dinucleotide synthetase deficiency', 'LIPID storage myopathy due to flavin adenine dinucleotide synthetase deficiency']",,255100,,,,,,C562935,,,,
mondo:0009704,"carnitine palmitoyl transferase II deficiency, myopathic form","['Carnitine palmitoyl transferase deficiency type 2, adult-onset form', 'Carnitine palmitoyl transferase deficiency type 2, myopathic form', 'CPT2, myopathic form', 'CARNITINE PALMITOYLTRANSFERASE II deficiency, myopathic, stress-induced', 'CPTII, adult-onset form', 'CPT2, adult-onset form', 'CARNITINE PALMITOYLTRANSFERASE II deficiency, late-onset', 'CPT 2 deficiency, myopathic', 'Carnitine Palmitoyltransferase 2 deficiency, adult-onset', 'Cpt2 deficiency, late-onset', 'CPTII, myopathic form', 'Carnitine palmitoyl transferase II deficiency, adult-onset form', 'CPT II deficiency, myopathic, stress-induced', 'Carnitine Palmitoyltransferase 2 deficiency, myopathic', 'Carnitine Palmitoyltransferase 2 deficiency, myopathic, stress-induced']",,255110,228302,C1833508,"['0.3535', '-0.01537', '-0.337', '0.3286', '0.1495', '-0.175', '0.2708', '0.4714', '-0.1854', '-0.1492', '0.0712', '-0.1017', '0.4087', '0.4417', '-0.6494', '-0.1722', '-0.01235', '-0.12115', '-0.4148', '-0.6797', '0.1044', '-0.4373', '0.689', '-0.3806', '-0.5366', '-0.2303', '-0.02928', '-0.253', '0.03226', '-0.2197', '0.316', '0.3867', '0.6724', '-0.4055', '-0.5723', '-0.7085', '-0.5454', '-0.3594', '-0.04816', '0.1781', '-0.0357', '-1.102', '0.7124', '0.2837', '0.2932', '0.3193', '0.1396', '-0.0796', '0.31', '1.221', '0.0408', '-0.2394', '0.1116', '-0.2295', '0.02571', '-0.3335', '0.628', '-0.2432', '0.04044', '0.02411', '0.3965', '0.2443', '0.5474', '-0.1289', '0.1848', '0.4375', '0.4888', '0.4766', '-0.4204', '-0.3728', '0.1882', '-0.06082', '0.289', '0.122', '0.764', '1.159', '0.04825', '0.0635', '0.1964', '0.3835', '0.5586', '-0.1263', '0.3293', '-0.1478', '0.315', '0.7334', '-0.4707', '0.3582', '0.6475', '-0.4702', '0.0051', '0.2944', '-0.02974', '0.1782', '0.457', '0.852', '0.2101', '-0.2489', '-0.5176', '-0.605']",,,C563461,,,,
mondo:0009705,carnitine palmitoyl transferase 1A deficiency,"['CPT I deficiency', 'Carnitine palmitoyl transferase 1 deficiency', 'carnitine palmitoyl transferase 1A deficiency', 'carnitine palmitoyltransferase I deficiency', 'L-CPT 1 deficiency', 'L-CPTI deficiency', 'CPT1A deficiency', 'Carnitine Palmitoyltransferase 1A deficiency', 'Carnitine palmitoyltransferase 1A deficiency', 'hepatic CPT1', 'carnitine palmitoyl transferase IA deficiency', 'CPT1A disorder of carnitine cycle and carnitine transport', 'CPT deficiency, hepatic, type 1', 'hepatic CPT deficiency type I', 'disorder of carnitine cycle and carnitine transport caused by mutation in CPT1A', 'Carnitine Palmitoyltransferase 1 deficiency', 'hepatic carnitine palmitoyltransferase 1 deficiency', 'cpt deficiency, hepatic, type IA', 'Carnitine palmitoyl transferase IA deficiency', 'hepatic carnitine palmitoyl transferase 1 deficiency', 'CPT 1 deficiency', 'L-CPT1 deficiency', 'hepatic carnitine palmitoyl transferase I deficiency']",0090129,255120,156,C1829703,"['0.2417', '0.2585', '-0.1685', '-0.2683', '-0.0006046', '-0.2617', '0.009995', '0.3357', '0.2869', '0.162', '-0.2815', '-0.4917', '0.3584', '0.3057', '-0.333', '-0.1968', '0.3162', '-0.2322', '-0.5337', '-0.8755', '0.319', '-0.5146', '0.5186', '-0.11273', '-0.2566', '-0.4644', '-0.2551', '0.0941', '-0.08136', '-0.1538', '0.8887', '0.2803', '0.387', '-0.10077', '-0.4426', '-0.4285', '-0.09265', '-0.05743', '-0.4072', '0.3735', '-0.241', '-0.8833', '0.923', '-0.2551', '-0.561', '-0.52', '0.1489', '-0.2961', '-0.01445', '0.8965', '-0.563', '-0.0284', '0.11957', '-0.3384', '0.1023', '-0.4944', '0.0828', '0.4373', '0.1053', '0.0911', '0.12305', '0.1523', '0.715', '-0.5376', '-0.2683', '-0.002861', '0.73', '0.3792', '-1.003', '-0.154', '0.2693', '-0.0955', '0.10284', '0.2397', '0.629', '0.2517', '0.2356', '0.0911', '0.1406', '0.2137', '0.2507', '-0.4045', '-0.001211', '-0.505', '0.6016', '0.6104', '-0.1584', '0.0346', '0.48', '-0.02701', '0.2927', '-0.129', '-0.367', '0.2229', '0.2598', '0.8647', '0.2117', '-0.911', '-0.099', '-0.09033']",C98871,,C535588,277.85,,,
mondo:0009706,hereditary myopathy with lactic acidosis due to ISCU deficiency,"['aconitase deficiency', 'iron-sulfur cluster deficiency myopathy', 'myopathy with deficiency of succinate dehydrogenase and aconitase', 'myoglobinuria due to abnormal glycolysis', 'myopathy with lactic acidosis, hereditary', 'ISCU myopathy', 'HML', 'myopathy with exercise intolerance, Swedish type']",,255125,43115,C1850718,"['-0.6157', '-0.1537', '-0.3455', '0.01852', '-0.3684', '-0.4678', '-0.02551', '0.9565', '-0.09106', '0.0652', '-0.3096', '0.09955', '-0.1486', '0.02995', '-0.1262', '0.554', '-0.2122', '0.04956', '-0.9873', '-0.4956', '0.4263', '-0.446', '0.1669', '-0.2107', '-0.3232', '-0.3079', '0.3472', '-0.0138', '-0.2473', '-0.5347', '-0.1516', '0.335', '0.3865', '0.4934', '-0.3484', '-0.513', '0.1016', '-0.1884', '0.1722', '0.0899', '0.03812', '-0.4949', '-0.1155', '0.2244', '0.04437', '0.1333', '-0.1808', '-0.002647', '-0.03204', '0.374', '-0.5186', '-0.319', '0.1936', '0.2837', '0.0102', '-0.554', '0.761', '-0.446', '0.0582', '0.0816', '0.02946', '-0.0929', '0.128', '-0.3079', '-0.489', '0.4292', '0.422', '0.8267', '-0.3896', '-0.2026', '-0.392', '0.1667', '-0.352', '0.079', '0.166', '0.2505', '0.1567', '0.02266', '-0.1619', '0.1705', '0.1389', '0.157', '0.0832', '0.1323', '0.2734', '0.416', '0.156', '0.09283', '0.4065', '-0.2313', '0.7573', '-0.277', '-0.00432', '-0.2493', '0.2776', '0.5776', '0.2455', '-0.5093', '-0.1738', '-0.4155']",,,C564972,259.8,,,
mondo:0009707,myopathy with giant abnormal mitochondria,['myopathy with giant abnormal mitochondria'],,255140,,C1850717,,,,C564971,,,,
mondo:0009708,"myopathy, myosin storage, autosomal recessive","['autosomal recessive myosin storage myopathy', 'MSMB', 'myopathy, hyaline body, autosomal recessive', 'myopathy, myosin storage, autosomal recessive']",0111268,255160,636970,C1850709,,,,C564970,,,,
mondo:0009709,"myopathy, centronuclear, 2","['myopathy, centronuclear, type 2', 'CNM2', 'centronuclear myopathy 2', 'centronuclear myopathy caused by mutation in BIN1', 'myopathy, centronuclear, autosomal recessive', 'myotubular myopathy, autosomal recessive', 'myopathy, centronuclear, 2', 'BIN1 centronuclear myopathy']",0111220,255200,,,,,,C562934,,,,
mondo:0009710,Thomsen and Becker disease,"['myotonia congenita', 'Batten-Turner congenital myopathy', 'myopathy, congenital']",2106,,614,C0027127,"['-0.279', '-0.167', '0.1364', '-0.4373', '-0.0104', '-0.02055', '0.3584', '0.649', '-0.4707', '-0.3455', '-0.51', '0.42', '-0.1697', '-0.1534', '0.1288', '0.128', '-0.636', '-0.4585', '-0.3218', '-1.067', '-0.422', '-0.4607', '0.5913', '-0.11456', '-0.1743', '0.03345', '0.209', '-0.7363', '-0.3037', '-0.4578', '-0.003904', '0.2247', '-0.2491', '0.1473', '-0.6445', '0.3242', '0.4739', '-0.1652', '0.3113', '-0.0263', '-0.2947', '-0.613', '0.0667', '0.408', '1.032', '0.05453', '-0.3523', '0.4807', '0.2401', '0.4338', '0.02812', '0.197', '0.2117', '-0.722', '0.0815', '-0.409', '0.435', '-0.11017', '-0.5347', '-0.187', '0.193', '0.2046', '0.03177', '-0.0335', '-0.07623', '0.04477', '0.7085', '-0.1195', '-0.3015', '-0.05432', '-0.52', '-0.5547', '0.1681', '0.346', '1.164', '0.6313', '-0.10443', '0.03616', '0.1847', '-0.4714', '0.4595', '0.01119', '0.444', '0.279', '0.2756', '0.6724', '0.2798', '0.0652', '0.6675', '0.3281', '-0.183', '-0.3372', '0.4082', '0.3594', '0.5464', '0.02754', '0.3794', '-0.1576', '-0.6045', '-0.4219']",C84912,,D009224,359.22,G71.12,10043461,
mondo:0009711,congenital fiber-type disproportion myopathy,"['myopathy, congenital with fiber-type disproportion', 'congenital fibre type disproportion', 'congenital myopathy with fibre type disproportion', 'CFTDM', 'congenital fiber type disproportion', 'congenital fiber-type disproportion', 'congenital myopathy with fiber type disproportion']",0080102,,2020,C0546264,"['-0.2238', '0.04306', '-0.3816', '-0.8403', '0.001586', '-0.8643', '0.4648', '0.9185', '-1.437', '-0.819', '0.2223', '-0.013916', '0.1725', '0.2527', '0.03008', '0.3743', '-0.04306', '-0.4207', '-0.517', '-0.777', '0.02599', '-0.1874', '0.08344', '0.2646', '-0.4116', '-0.001972', '-0.0641', '-0.3213', '-0.01944', '-0.05612', '0.1978', '0.151', '0.1267', '-0.05103', '-0.086', '-0.1671', '-0.1511', '-0.2708', '0.4048', '0.07623', '0.1643', '0.02428', '-0.0796', '0.574', '-0.4595', '0.156', '-0.2554', '0.1107', '0.5386', '0.3816', '-0.484', '-0.3186', '0.2402', '-0.6445', '-0.1838', '-0.5503', '0.719', '0.2554', '0.2363', '0.02612', '0.1705', '0.1849', '-0.2563', '0.4639', '-0.764', '0.4138', '-0.28', '0.3633', '-0.3381', '0.10095', '-0.5166', '-0.01846', '-0.04922', '0.2622', '0.1901', '0.3066', '-0.1556', '-0.3179', '-0.553', '-0.1932', '-0.1039', '-0.353', '0.6167', '0.07556', '-0.2107', '1.001', '-0.06775', '0.5825', '-0.1168', '0.1724', '-0.07104', '0.0322', '-0.05453', '-0.1989', '0.259', '-0.0655', '0.656', '-0.455', '0.02365', '0.1853']",C120046,,,,,,
mondo:0009712,congenital multicore myopathy with external ophthalmoplegia,"['minicore myopathy', 'multicore myopathy with external ophthalmoplegia', 'minicore myopathy with external ophthalmoplegia', 'multicore myopathy', 'multiminicore disease with external ophthalmoplegia', 'minicore myopathy, antenatal onset, with arthrogryposis', 'multiminicore myopathy multicore myopathy with external ophthalmoplegia']",,255320,98905,C1850674,"['-0.431', '0.3137', '0.1638', '-0.3408', '0.06033', '-0.279', '-0.166', '0.1978', '-0.3755', '-0.08105', '-0.1913', '0.0718', '0.07886', '-0.2634', '0.04926', '0.2306', '0.03772', '-0.1881', '-0.2096', '-0.496', '0.2144', '-0.1387', '0.2727', '0.0936', '0.08124', '0.01656', '0.3025', '0.1183', '-0.1646', '-0.1448', '0.11914', '0.1838', '0.2305', '-0.10144', '-0.095', '-0.1032', '-0.1104', '0.0137', '0.00885', '-0.31', '0.08685', '-0.472', '-0.2124', '0.4253', '-0.1625', '-0.3843', '0.005375', '0.2976', '0.2559', '0.2103', '-0.1989', '-0.038', '-0.03217', '0.11035', '-0.0747', '-0.525', '0.509', '0.01211', '-0.318', '0.202', '-0.05246', '0.2401', '0.10004', '-0.004955', '-0.222', '0.2354', '0.2417', '0.1544', '-0.2161', '-0.00959', '-0.1803', '-0.0461', '0.2585', '0.1394', '0.1617', '0.0758', '0.1954', '0.2158', '-0.3015', '-0.0456', '0.317', '0.1908', '0.2284', '0.1355', '0.002396', '0.0397', '-0.0808', '0.386', '0.2223', '0.01294', '0.1787', '0.3054', '0.1398', '-0.1376', '0.3474', '0.231', '0.326', '-0.08875', '0.1321', '-0.02588']",C150608,,,,,,
mondo:0009713,"myopia 18, autosomal recessive","['MYP18', 'myopia 18, autosomal recessive']",,255500,,C2749509,,,,C567606,,,,
mondo:0009714,myosclerosis,"['congenital myosclerosis, LC6wenthal type', 'myopathy, myosclerotic', 'myosclerosis, congenital, of Lowenthal', 'congenital myosclerosis, Löwenthal type', 'myosclerosis, autosomal recessive', 'myosclerosis, congenital']",,255600,289380,,"['-0.6655', '-0.1625', '0.01353', '-0.282', '0.03223', '-0.9067', '0.02281', '0.622', '-1.0', '0.07806', '-0.3232', '0.129', '-0.03598', '-0.2496', '0.348', '-0.09296', '-0.04425', '-0.3352', '-0.2595', '-1.126', '0.1428', '0.1715', '0.5894', '0.63', '0.02371', '0.2185', '0.511', '0.2167', '-0.0964', '0.1516', '-0.0332', '-0.316', '-0.2246', '0.1737', '-0.1348', '-0.2832', '0.116', '0.2416', '0.3025', '-0.3774', '-0.1576', '-0.801', '-0.4604', '0.7827', '-0.4873', '0.11334', '-0.2133', '-0.2917', '0.776', '0.0452', '-0.1301', '-0.3877', '0.246', '0.1287', '-0.0923', '-0.6875', '0.5566', '-0.3271', '-0.03888', '-0.2688', '-0.05194', '0.2452', '-0.1935', '0.02032', '-0.2957', '0.083', '0.265', '0.688', '-0.4417', '0.2405', '-0.342', '0.01518', '0.04315', '0.268', '0.2101', '0.01378', '0.1108', '0.2449', '0.0427', '0.01738', '-0.0686', '-0.3352', '0.4355', '0.3547', '-0.4973', '0.07556', '-0.3696', '0.3047', '0.499', '-0.1589', '0.0486', '0.328', '0.328', '0.3352', '0.4246', '0.216', '0.6025', '-0.4312', '0.08496', '-0.2126']",,,C564968,,,10064584,
mondo:0009715,"myotonia congenita, autosomal recessive","['myotonia, generalized', 'myotonia congenita, recessive', 'autosomal recessive myotonia congenita', 'myotonia congenita, autosomal recessive', 'Becker disease', 'myotonia, generalised']",,255700,,C0751360,,,,,,,,
mondo:0009716,Richieri Costa-da Silva syndrome,"['myotonia with skeletal abnormalities and intellectual disability', 'Richieri Costa Da Silva syndrome', 'myotonia-intellectual disability-skeletal anomalies syndrome', 'myotonia with skeletal abnormalities and mental retardation']",,255710,3101,C2930978,,,,C535675,,,,
mondo:0009717,Schwartz-Jampel syndrome,"['myotonic myopathy dwarfism chondrodystrophy and ocular and facial abnormalities', 'SJS', 'myotonic myopathy, dwarfism, chondrodystrophy, and ocular and Facial abnormalities', 'Schwartz Jampel Aberfeld syndrome', 'Catel-Hempel type dysostosis enchondralis metaepiphysaria', 'myotonic chondrodystrophy', 'Schwartz-Jampel-Aberfeld syndrome', 'Schwartz Jampel syndrome', 'Aberfeld syndrome', 'Schwartz-Jampel syndrome', 'burton skeletal dysplasia', 'dysostosis enchondralis metaepiphysaria, Catel-Hempel type', 'myotonic myopathy, dwarfism, chondrodystrophy, ocular and facial anomalies', 'burton syndrome', 'Osteochondromuscular dystrophy', 'Catel-Hempel syndrome', 'osteochondromuscular dystrophy']",,,800,C0036391,"['-0.3716', '-0.000602', '-0.0652', '-0.333', '-0.385', '-0.2427', '0.665', '1.376', '-0.953', '-0.2054', '-0.4275', '0.7124', '0.4392', '-0.05908', '-0.0715', '0.3484', '-0.125', '-0.2847', '-0.1478', '-0.73', '0.1882', '0.08795', '0.4949', '-0.365', '-0.641', '-0.332', '-0.3196', '0.01859', '-0.04013', '-0.3572', '0.5493', '0.113', '0.1769', '0.2092', '-0.08215', '-0.2715', '0.2625', '-1.229', '-0.05344', '0.198', '0.6826', '-0.567', '-0.003994', '-0.03143', '0.21', '-0.079', '0.1796', '0.255', '0.0392', '0.1404', '-0.2294', '0.007015', '0.4587', '0.1765', '0.1184', '-0.917', '0.1332', '-0.04492', '0.309', '-0.228', '0.1481', '0.3408', '-0.908', '0.357', '-0.512', '0.11743', '0.3032', '-0.2335', '-0.1832', '0.4258', '0.0926', '-0.1266', '0.287', '-0.5977', '0.1848', '-0.2446', '0.1514', '0.1087', '-0.3618', '-0.2961', '0.5327', '-0.282', '-0.3833', '0.6064', '-0.478', '0.3274', '-0.5835', '0.61', '0.2242', '-0.2115', '0.1328', '0.1691', '0.784', '0.2235', '0.501', '-0.4136', '0.2368', '-0.259', '0.323', '-0.5703']",C35008,,,759.89,,,
mondo:0009718,myxedema,['myxedema'],11634,255900,,C0027145,,C34834,1001055,D009230,,,10028663,
mondo:0009719,familial atrial myxoma,"['atrial Myxoma, familial', 'intracardiac myxoma', 'MYXOMA, intracardiac']",,255960,615,C1850635,"['-0.3833', '0.04187', '-0.2502', '0.2228', '0.1786', '-0.0708', '0.344', '0.12225', '-0.1395', '0.2006', '-0.304', '0.12067', '-0.06128', '-0.02371', '-0.291', '0.1167', '-0.264', '0.07434', '0.1754', '-0.4592', '0.2688', '0.03906', '0.3147', '-0.2157', '-0.02701', '-0.0846', '0.08154', '0.1304', '0.02335', '0.1025', '0.5806', '0.03232', '0.4187', '-0.258', '-0.07117', '-0.1866', '-0.2062', '-0.02338', '-0.02943', '-0.3826', '0.2277', '-0.2898', '0.2118', '-0.2465', '0.04727', '0.2673', '-0.2314', '0.0945', '0.1007', '0.0869', '-0.01944', '0.2346', '0.1997', '0.2198', '-0.1733', '-0.1532', '-0.1298', '0.0251', '-0.2705', '-0.1584', '0.2327', '0.010765', '-0.2822', '-0.3867', '-0.2148', '0.03174', '0.477', '0.7007', '-0.212', '0.3276', '-0.1033', '0.05777', '-0.06042', '0.02953', '-0.05792', '-0.0149', '0.1082', '0.1538', '0.01941', '-0.5293', '-0.321', '-0.1316', '0.1192', '0.06396', '-0.0326', '-0.1256', '0.2551', '0.06616', '0.135', '-0.2363', '0.2341', '0.06976', '0.2527', '-0.02484', '0.5034', '0.1274', '0.4087', '-0.11646', '-0.2252', '0.2522']",,,C538262,,D15.1,,
mondo:0009720,Keipert syndrome,"['Keipert syndrome', 'nasodigitoacoustic syndrome, formerly', 'Keipert syndrome, X-linked recessive', 'KPTS', 'nasodigitoacoustic syndrome']",0111842,301026,2662,C1850627,"['-0.296', '-0.04272', '0.3125', '-0.512', '-0.2476', '-0.37', '0.1952', '0.6323', '-0.2964', '-0.12067', '0.3225', '-0.619', '-0.1277', '0.1434', '-0.642', '-0.03635', '0.2888', '-0.0733', '-0.2935', '-0.199', '-0.1769', '0.03442', '-0.003546', '-0.1472', '0.6914', '-0.2444', '-0.1076', '0.09894', '0.8696', '-0.4233', '0.3696', '-0.2544', '0.58', '0.5767', '0.5137', '-0.829', '-0.2812', '-0.2566', '0.01964', '-0.608', '0.04507', '-0.02313', '0.2064', '-0.5093', '0.014145', '-0.2693', '-0.264', '0.626', '-0.5146', '-0.1058', '-0.4172', '0.413', '-0.1847', '0.241', '-0.51', '-0.6724', '-0.4565', '-0.2076', '0.02838', '-0.04047', '0.1594', '0.2075', '-0.5547', '-0.1865', '-0.2712', '-0.325', '0.4534', '0.4568', '-0.5786', '0.493', '-0.6343', '0.3425', '0.3184', '-0.1411', '0.04648', '0.2578', '0.09784', '-0.1603', '-0.4265', '0.2207', '0.02878', '0.04544', '0.02695', '0.842', '-0.3608', '0.283', '-0.0894', '0.469', '0.01338', '-0.0629', '-0.0841', '0.4082', '0.479', '0.8267', '1.069', '-0.1628', '0.618', '-0.527', '0.3706', '0.5703']",C186306,,C538337,,,,
mondo:0009721,Nathalie syndrome,"['sensorineural hearing loss-cataract-skeletal anomalies-cardiomyopathy syndrome', 'deafness-cataract-skeletal anomalies syndrome', 'deafness, cataract, muscular atrophy, skeletal abnormalities, growth retardation, underdeveloped secondary sexual characteristics', 'deafness-cataracts-skeletal anomalies syndrome', 'Nathalie syndrome']",,255990,2663,C1850626,,,,C538342,,,,
mondo:0009722,Bailey-Bloch congenital myopathy,"['congenital myopathy-cleft palate-malignant hyperthermia syndrome', 'STAC3 disorder', 'myopathy, congenital, baily-bloch', 'NAM', 'Native American myopathy', 'congenital myopathy - cleft palate - malignant hyperthermia', 'myopathy, congenital, with cleft palate and malignant hyperthermia', 'congenital myopathy cleft palate and malignant hyperthermia']",0060346,255995,168572,C1850625,"['-0.4683', '0.386', '-0.1498', '-0.571', '0.7144', '-0.9185', '0.2084', '0.7', '-0.1329', '-0.525', '0.4692', '0.5454', '-0.04175', '-0.2737', '-0.2441', '0.4792', '0.225', '-0.284', '-0.5605', '-0.4827', '-0.06537', '-0.2756', '0.4336', '-0.1986', '-0.6294', '-0.1421', '-0.03467', '-0.03024', '-0.1487', '-0.5444', '0.02856', '0.0499', '0.262', '0.113', '-0.1729', '-0.1045', '0.349', '-0.4116', '-0.05453', '0.0776', '-0.2979', '-0.1118', '0.2299', '-0.0392', '-0.3098', '0.10254', '0.5327', '0.4556', '0.2722', '-0.1112', '-0.3152', '-0.3274', '-0.1396', '-0.2778', '0.3347', '-0.584', '0.506', '-0.5596', '-0.2472', '-0.2563', '0.605', '0.3115', '-0.11176', '0.629', '-0.286', '0.1715', '0.2874', '0.3503', '-0.6924', '0.6147', '-0.4075', '-0.2576', '0.1489', '-0.09656', '-0.04495', '0.3823', '-0.0828', '0.2961', '-0.3684', '0.10345', '0.3584', '0.0721', '0.0366', '0.826', '-0.4675', '0.171', '0.05655', '0.1592', '-0.1058', '-0.4434', '0.4575', '0.2028', '0.761', '0.03937', '0.794', '-0.4094', '0.726', '-0.1737', '-0.2654', '-0.1937']",,,C538343,,,,
mondo:0009723,Leigh syndrome,"['Leigh syndrome due to mitochondrial Complex 3 deficiency', 'Leigh syndrome due to mitochondrial Complex 4 deficiency', 'LSS', 'Leigh^s disease', 'Leigh syndrome due to mitochondrial Complex 2 deficiency', 'subacute necrotizing encephalomyelopathy', 'Leigh syndrome spectrum', 'necrotizing encephalopathy, infantile Subacute, of Leigh', 'LS', 'Leigh syndrome', 'Leigh^s necrotizing encephalopathy', 'SNE', 'juvenile subacute necrotizing encephalomyelopathy', 'infantile necrotizing encephalomyelopathy', 'Leigh syndrome due to mitochondrial Complex 1 deficiency', 'Leigh disease', 'Leigh syndrome due to mitochondrial Complex 5 deficiency', 'subacute necrotizing encephalopathy', 'infantile subacute necrotizing encephalopathy']",3652,256000,506,C0023264,"['-0.5317', '0.204', '-0.2769', '-0.1013', '-0.156', '-0.3228', '-0.09546', '0.321', '-0.1368', '-0.196', '-0.9404', '-0.568', '0.214', '-0.05133', '0.5737', '0.1984', '-0.0733', '-0.479', '-0.4631', '-0.566', '0.09326', '-0.6294', '0.4492', '-0.01917', '0.1483', '-0.04037', '0.10284', '0.2754', '-0.534', '0.192', '0.3606', '0.666', '0.2854', '0.2031', '0.1576', '0.2869', '-0.0712', '-0.2966', '-0.02673', '0.5713', '0.0489', '-0.7188', '0.4114', '0.08936', '0.1373', '-0.7866', '0.3738', '0.0559', '-0.1311', '0.331', '-0.08344', '0.07434', '-0.683', '-0.477', '0.5684', '-0.692', '0.6562', '0.0519', '0.184', '0.345', '0.1393', '-0.3408', '0.3457', '-0.2769', '-0.726', '0.3796', '0.6514', '0.2812', '-0.4136', '0.975', '-0.10504', '0.05347', '-0.4478', '-0.466', '0.4258', '0.3489', '0.2385', '-0.1122', '-0.10315', '0.345', '0.1661', '-0.3784', '-0.251', '0.667', '-0.0632', '-0.03717', '0.2085', '0.504', '0.458', '-0.0735', '0.364', '0.368', '0.0781', '-0.0493', '0.01276', '0.1649', '0.4592', '0.06946', '0.151', '-0.4187']",C84814,,D007888,330.8,,10062950,
mondo:0009724,nail-patella-like renal disease,"['nail patella like renal disease', 'nail-patella-like renal disease', 'glomerular basement Membrane disease, nail-patella syndrome type', 'focal segmental glomerulosclerosis 10', 'Salcedo syndrome']",,256020,2613,C0403548,,,,C537228,756.89,,,
mondo:0009725,nemaline myopathy 2,"['nemaline myopathy caused by mutation in NEB', 'NEM2', 'nemaline myopathy 2', 'nemaline myopathy 2, autosomal recessive', 'nemaline myopathy type 2', 'NEB nemaline myopathy']",0110928,256030,,CN187052,,C118784,,C538349,,,,
mondo:0009726,proteosome-associated autoinflammatory syndrome,"['Joint contractures, muscular atrophy, microcytic Anemia, and panniculitis-induced lipodystrophy', 'Joint contractures - muscle atrophy - microcytic anemia - panniculitis-induced lipodystrophy', 'amyotrophy-fat tissue anomaly syndrome', 'autoinflammation, lipodystrophy, and dermatosis syndrome', 'Nakajo syndrome', 'autoinflammation-lipodystrophy-dermatosis syndrome', 'CANDLE syndrome', 'Nakajo-Nishimura syndrome', 'ALDD syndrome', 'chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature syndrome', 'Nakajo Nishimura syndrome', 'proteasome disability syndrome', 'Joint contractures-muscular atrophy-microcytic anemia-panniculitis-associated lipodystrophy syndrome', 'chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature', 'ALDD', 'secondary hypertrophic osteoperiostosis with pernio', 'amyotrophy fat tissue anomaly', 'chronic atypical neutrophilic dermatosis-lipodystrophy-elevated temperature syndrome', 'joint contractures, muscular atrophy, microcytic anemia, and panniculitis-induced lipodystrophy', 'Joint contractures - muscle atrophy - microcytic anaemia - panniculitis-induced lipodystrophy', 'PRAAS', 'nodular erythema digital changes', 'JMP syndrome', 'NNS', 'proteasome-associated autoinflammatory syndrome']",0050553,,325004,CN204109,"['0.1332', '0.2598', '-0.2678', '-0.3982', '0.2156', '-0.752', '0.1654', '0.7007', '-0.4495', '-0.3687', '-0.656', '0.4048', '-0.006123', '0.6504', '-0.1963', '0.6777', '0.5815', '0.1958', '-0.094', '-1.055', '-0.003864', '-0.7905', '0.2283', '-0.2937', '0.1134', '0.2668', '-0.2864', '0.3086', '-0.1724', '-0.449', '0.2157', '-0.566', '0.1909', '0.3806', '-0.0006676', '0.0753', '-0.455', '-0.347', '-0.206', '0.521', '-1.042', '-0.84', '0.11957', '-0.1586', '0.8643', '0.1287', '-0.3457', '0.4543', '-0.1298', '0.06836', '-0.2605', '0.372', '0.648', '0.6006', '-0.5044', '-0.2568', '-0.2688', '-0.0831', '-0.1153', '0.03998', '-0.1039', '0.465', '-0.599', '-0.1865', '-0.0891', '0.2096', '0.3145', '0.1926', '0.5894', '0.769', '-0.152', '-0.07623', '0.1848', '-0.1122', '0.0846', '0.415', '0.55', '-0.3857', '0.1886', '-0.571', '0.4697', '-0.3423', '0.2903', '0.3564', '-0.04654', '0.3333', '0.08044', '0.4873', '-0.02989', '0.656', '0.9346', '-0.1567', '0.1964', '-0.04645', '0.532', '0.1986', '0.556', '-0.2415', '0.136', '-0.2194']",,,C538334,709.8,,,
mondo:0009727,atelosteogenesis type II,"['De 50A Chapelle dysplasia', 'AOII', 'AO2', 'neonatal osseous dysplasia 1', 'atelosteogenesis II', 'atelosteogenesis, type 2', 'atelosteogenesis, type II', 'De la Chapelle dysplasia', 'neonatal osseous dysplasia type 1', 'atelosteogenesis type 2']",,256050,56304,C1850555,"['-0.4045', '0.3062', '0.3657', '-0.2842', '0.431', '-0.329', '-0.201', '0.4827', '-0.58', '-0.2247', '-0.2793', '0.0742', '0.453', '-0.0747', '-0.05405', '0.1201', '0.07434', '-0.3135', '-0.372', '-0.3386', '0.2776', '0.04037', '0.863', '-0.0003164', '0.2563', '0.10364', '-0.0621', '0.007378', '0.3862', '-0.1206', '-0.09', '-0.0003738', '0.2893', '0.084', '0.08307', '-0.404', '0.104', '-0.1936', '-0.02469', '-0.6343', '-0.0666', '-0.365', '0.1356', '-0.1296', '-0.2742', '-0.3867', '0.05865', '0.3337', '0.2341', '-0.09467', '-0.2446', '-0.5547', '-0.0538', '0.10065', '-0.2152', '-0.6953', '0.08685', '-0.3047', '0.0651', '0.2542', '0.379', '0.1847', '-0.1484', '0.07385', '-0.1333', '-0.269', '0.06137', '0.2301', '-0.4146', '0.0826', '-0.561', '0.0314', '0.3125', '0.1027', '-0.2157', '0.08844', '-0.0332', '0.1284', '-0.3645', '-0.2886', '-0.04376', '0.3064', '-0.0894', '0.2935', '-0.514', '0.3228', '0.1076', '0.559', '0.366', '0.07104', '-0.3098', '0.2119', '0.3376', '0.1404', '0.508', '0.3057', '0.697', '-0.5454', '0.509', '0.261']",,,C535395,756.9,Q77.5,,
mondo:0009728,nephronophthisis 1,"['NPH1', 'nephronophthisis type 1', 'NPHP1', 'NPHP1 nephronophthisis (disease)', 'nephronophthisis 1', 'nephronophthisis, familial juvenile', 'nephronophthisis 1, juvenile', 'familial juvenile nephronophthisis', 'Nph1', 'juvenile nephronophthisis', 'juvenile nephronophthisis 1']",0111112,256100,93592,CN205459,"['-0.1038', '0.1259', '-0.0925', '-0.01543', '0.094', '-0.3384', '-0.2203', '0.2228', '-0.1761', '-0.1553', '-0.1307', '-0.09155', '-0.1263', '0.03766', '-0.07404', '-0.2448', '-0.03397', '-0.03537', '-0.004612', '-0.4646', '0.04953', '-0.288', '-0.05127', '-0.08307', '0.2096', '-0.0963', '-0.03986', '0.1043', '-0.1298', '-0.1271', '0.1055', '0.03021', '0.259', '0.2605', '-0.06046', '-0.2169', '-0.00646', '-0.02316', '-0.08374', '0.1576', '-0.2788', '-0.127', '0.3367', '0.07666', '-0.1569', '-0.152', '-0.2413', '-0.0622', '0.09546', '0.01534', '0.1268', '0.06885', '0.0997', '-0.05075', '0.1462', '-0.351', '0.2888', '0.05316', '-0.4722', '0.1522', '0.3628', '0.1438', '0.10675', '-0.06537', '0.1222', '-0.184', '0.368', '0.4373', '-0.2351', '0.2334', '-0.2861', '-0.2103', '0.2286', '-0.00847', '0.2351', '-0.03055', '0.09296', '0.264', '-0.1388', '0.02573', '0.0961', '-0.02542', '0.0707', '0.1321', '-0.03796', '0.01204', '0.2983', '-0.02106', '0.1902', '0.1024', '0.1221', '0.2769', '-0.0687', '-0.11786', '0.487', '0.2356', '0.3887', '-0.0825', '-0.0917', '0.1709']",C74998,,C537699,,,,
mondo:0009729,nephropathy - deafness - hyperparathyroidism syndrome,"['nephropathy, deafness, and hyperparathyroidism', 'Edwards-Patton-Dilly syndrome', 'Edwards Patton Dilly syndrome', 'nephropathy - deafness - hyperparathyroidism']",,256120,2668,C1850553,,,,C536401,,,,
mondo:0009731,nephrosis-deafness-urinary tract-digital malformations syndrome,"['nephrosis deafness urinary tract digital malformation', 'nephrosis with deafness and urinary tract and digital malformations', 'Braun-Bayer syndrome']",,256200,2669,C1850552,,,,C536402,,,,
mondo:0009732,"congenital nephrotic syndrome, Finnish type","['congenital nephrotic syndrome - Finnish type', 'nephrotic syndrome - NPHS1 associated', 'nephrotic syndrome, congenital', 'congenital nephrotic syndrome Finnish type', 'CnF', 'Finnish congenital nephrosis', 'congenital nephrotic syndrome 1', 'nephrosis 1, congenital, Finnish type', 'NPHS1', 'nephrotic syndrome, type 1', 'nephrosis, congenital']",0080390,256300,839,C0403399,"['0.4648', '-0.3374', '-0.0712', '-0.1456', '-0.4634', '-0.3264', '-0.003624', '0.3567', '-0.303', '-0.711', '0.2158', '-0.09015', '-0.42', '0.8477', '-0.9023', '0.1654', '-0.1908', '0.1785', '0.6636', '-0.484', '1.058', '-0.9604', '0.725', '0.3743', '0.12036', '-0.3647', '-0.422', '0.516', '-0.01214', '-0.6064', '1.116', '-0.1633', '1.011', '0.1913', '-0.3906', '-0.03925', '-0.2362', '0.4888', '0.1003', '-0.1656', '-0.498', '0.451', '-0.10645', '-0.506', '-0.1284', '-0.0708', '-0.2505', '-0.2113', '-0.2181', '-0.25', '-0.2927', '0.1796', '1.103', '-0.9697', '-0.3813', '-0.44', '0.261', '-0.09906', '-0.815', '-0.1051', '-0.4812', '-0.1062', '0.1198', '-0.5854', '0.1548', '-0.3025', '0.9634', '-0.06238', '-0.968', '0.197', '-0.00815', '0.4333', '0.3726', '0.013885', '0.424', '0.07184', '0.204', '0.6963', '-0.407', '0.1268', '0.0628', '-0.02621', '0.1642', '-0.1726', '-0.2576', '-0.0886', '0.176', '-0.2952', '0.271', '0.1001', '0.5728', '0.7207', '-0.6777', '-0.516', '0.3906', '0.2917', '0.005802', '-0.8438', '0.1785', '-0.454']",C122795,,,,,10060740,
mondo:0009733,"nephrotic syndrome, type 4","['mesangial sclerosis, diffuse', 'diffuse mesangial sclerosis', 'nephrotic syndrome, early onset with diffuse mesangial sclerosis', 'isolated diffuse mesangial sclerosis', 'nephrotic syndrome caused by mutation in WT1', 'congenital nephrotic syndrome - diffuse mesangial sclerosis', 'NPHS4', 'familial mesangial sclerosis', 'DMS', 'nephrotic syndrome, type 4', 'WT1 nephrotic syndrome', 'diffuse isolated mesangial sclerosis']",0080383,256370,,C3151568,,C121198,,,,,,
mondo:0009734,"hyperinsulinemic hypoglycemia, familial, 1","['hyperinsulinemic hypoglycemia, familial, 1', 'Nesidioblastosis of pancreas', 'persistent hyperinsulinemic hypoglycemia of infancy', 'hyperinsulinism, congenital', 'HHF1', 'ABCC8 hyperinsulinemic hypoglycemia (disease)', 'hyperinsulinemic hypoglycemia, familial, type 1', 'hyperinsulinemic hypoglycemia due to focal adenomatous hyperplasia', 'hyperinsulinism, familial, with pancreatic Nesidioblastosis', 'hypoglycemia, hyperinsulinemic, of infancy', 'hyperinsulinemic hypoglycemia due to SUR1 deficiency']",0070219,256450,276575,C2931833,"['-0.02', '0.07635', '-0.008316', '-0.01176', '-0.002098', '-0.0758', '0.03525', '0.08246', '-0.05008', '-0.0178', '-0.026', '-0.00842', '0.001039', '0.01316', '-0.04697', '-0.05725', '-0.008675', '-0.0355', '-0.01628', '-0.12225', '0.01762', '-0.03622', '0.0531', '-0.02097', '0.00632', '-0.00811', '-0.002743', '-0.02205', '-0.007378', '-0.0531', '0.07764', '0.00391', '0.07477', '0.0366', '-0.004055', '-0.0176', '-0.014084', '-0.0364', '-0.01192', '-0.03717', '0.04285', '-0.0851', '0.03397', '-0.01049', '-0.005795', '-0.06107', '-0.03598', '0.06384', '0.01194', '0.05588', '-0.01918', '0.009094', '0.04135', '-0.01076', '-0.0388', '-0.03087', '0.0701', '-0.04523', '-0.08966', '0.01729', '0.04092', '0.044', '0.03093', '-0.02397', '0.00199', '0.01055', '0.0915', '0.04254', '-0.0958', '0.08234', '-0.05054', '0.01544', '0.03033', '-0.0783', '0.044', '0.05966', '0.00798', '0.02759', '-0.0541', '-0.02634', '4.97e-05', '0.01993', '-0.03943', '0.007652', '0.010796', '0.0253', '0.02542', '0.06052', '0.12177', '0.00524', '0.03014', '0.03403', '0.01576', '-0.02325', '0.1512', '0.0458', '0.05936', '-0.1198', '-0.03195', '0.03418']",,,,,,,
mondo:0009735,Netherton syndrome,"['Netherton syndrome', 'erythroderma, ichthyosiform, with hypotrichosis and hyper-IgE', 'NS', 'Comel-Netherton syndrome', 'bamboo hair syndrome', 'neth', 'Comèl-Netherton syndrome', 'Netherton disease']",0050474,256500,634,,"['0.1578', '0.06125', '-0.3623', '-0.4185', '0.1742', '-0.308', '-0.464', '0.3027', '0.1141', '-0.211', '-0.006195', '0.143', '0.2346', '-0.129', '-0.7827', '0.4902', '0.5376', '-0.0734', '-0.4219', '-0.905', '-0.5034', '-0.1709', '1.01', '-0.605', '0.1902', '-0.1378', '-0.1272', '-0.1328', '0.0932', '-0.9233', '0.642', '-0.341', '0.3386', '0.6123', '0.01848', '0.2239', '0.02043', '0.0633', '-0.01318', '0.2417', '0.2255', '-0.2318', '0.2815', '-0.0842', '0.4612', '-0.1471', '0.633', '-0.02667', '0.03555', '0.08276', '-0.1678', '-0.1555', '0.336', '0.03717', '0.12115', '0.1156', '0.2556', '0.1586', '-0.282', '-0.2472', '0.2324', '0.522', '-0.09717', '-0.322', '0.6177', '-0.3398', '0.7285', '0.01973', '-0.3164', '1.199', '-0.3289', '-0.559', '-0.0755', '0.3423', '0.01598', '0.04996', '0.1117', '-0.3872', '0.4531', '0.05283', '0.4202', '-0.008385', '-0.347', '0.0983', '-0.2725', '0.4854', '0.3645', '0.1617', '0.3599', '0.628', '0.4136', '0.38', '0.367', '0.4968', '-0.0692', '-0.02148', '0.1877', '-0.4185', '0.2495', '0.167']",C84922,,D056770,,,10062909,
mondo:0009736,Neu-Laxova syndrome 1,"['Neu-Laxova syndrome type 1', 'NLS1', 'Neu-Laxova syndrome due to 3-phosphoglycerate dehydrogenase deficiency', '3-phosphoglycerate dehydrogenase deficiency, prenatal form', '3-Phosphoglycerate dehydrogenase deficiency, neonatal form', 'Neu-Laxova syndrome caused by mutation in PHGDH', 'PHGDH Neu-Laxova syndrome', 'Neu-Laxova syndrome 1', 'Neu-Laxova syndrome']",0080076,256520,583607,CN032230,,,,,,,,
mondo:0009737,galactosialidosis,"['lysosomal protective Protein deficiency', 'lysosomal protective protein deficiency of', 'galactosialidosis', 'neuraminidase/Beta-galactosidase expression', 'cathepsin A deficiency of', 'PPCA deficiency', 'neuraminidase deficiency with beta-galactosidase deficiency', 'protective Protein/Cathepsin a deficiency', 'GSL', 'cathepsin A deficiency', 'Goldberg syndrome']",0080540,256540,351,C0268233,"['-0.471', '0.44', '0.1924', '0.1295', '0.2223', '-0.4397', '-0.3005', '-0.0786', '-0.2954', '-0.182', '-0.00561', '0.4143', '0.03934', '-0.1239', '0.2151', '-0.2766', '0.1351', '-0.1167', '-0.0836', '-0.2185', '-0.03357', '-0.0693', '0.3367', '0.1317', '0.01715', '0.03253', '-0.05264', '-0.056', '-0.215', '-0.1348', '0.2954', '0.259', '0.3894', '0.1641', '0.02628', '-0.17', '-0.1621', '0.0816', '-0.01119', '-0.5234', '-0.04498', '-0.563', '0.2925', '0.3127', '-0.1908', '-0.2369', '-0.1106', '0.08734', '0.0474', '-0.05865', '0.0876', '0.1448', '-0.0626', '0.03854', '0.3286', '-0.6978', '0.3657', '-0.05527', '-0.1604', '0.00489', '-0.05664', '-0.05328', '0.2766', '-0.1571', '0.4731', '-0.07214', '0.406', '0.1475', '-0.0511', '0.1781', '-0.261', '-0.1807', '0.3745', '0.2607', '0.1528', '0.2593', '0.0903', '0.2484', '-0.3057', '-0.2969', '0.1317', '-0.3735', '-0.1964', '0.4175', '0.2722', '0.104', '-0.05038', '0.12036', '0.5303', '0.2134', '0.2031', '0.3264', '0.00151', '0.1411', '0.2708', '0.4048', '0.4136', '-0.5225', '0.455', '0.1481']",C129928,,C536411,277.6,,,
mondo:0009738,sialidosis type 2,"['NEU 1 deficiency', 'cherry Red spot--myoclonus syndrome', 'neuraminidase 1 deficiency', 'mucolipidosis 1', 'sialidosis, type II', 'sialidosis, type 2', 'nephrosialidosis', 'mucolipidosis I', 'Neu1 deficiency', 'mucolipidosis type I', 'Neug deficiency', 'glycoprotein neuraminidase deficiency', 'myoclonus--cherry Red spot syndrome', 'lipomucopolysaccharidosis', 'sialidase deficiency', 'mucolipidosis type 1', 'ML 1', 'sialidosis caused by mutation in NEU1', 'NEU1 sialidosis', 'glycoproteinosis', 'neuraminidase deficiency', 'sialidosis', 'sialidosis type II', 'sialidosis, type 1', 'infantile dysmorphic sialidosis', 'sialidosis, type I', 'ML1', 'Neu deficiency']",3343,256550,87876,CN206285,"['-0.2769', '0.3008', '0.1024', '0.339', '-0.04916', '-0.915', '0.2766', '0.9497', '-0.9727', '-0.499', '-0.4956', '-0.1328', '-0.0993', '-0.1375', '0.159', '-0.0973', '0.3032', '-0.4626', '-0.1372', '-0.3816', '-0.1274', '-0.3257', '0.4531', '-0.4836', '-0.2532', '0.1399', '-0.3992', '0.4094', '-0.3547', '0.6606', '0.967', '0.0384', '0.2786', '0.02603', '-0.10345', '-0.3447', '-0.2559', '-0.3862', '-0.1384', '-0.1671', '0.1855', '-0.56', '0.777', '0.3938', '0.05392', '-0.151', '0.02907', '-0.1543', '0.2368', '-0.4172', '0.3677', '0.4336', '-0.225', '0.1283', '0.8135', '-0.4995', '-0.12415', '-0.525', '-0.3335', '0.1104', '-0.2474', '-0.574', '0.2756', '-0.1732', '0.5767', '-0.6343', '0.8555', '-0.6274', '-0.4463', '-0.06635', '0.015594', '-0.6206', '0.3293', '0.5195', '0.11694', '0.0473', '0.0678', '-0.1678', '-0.488', '-0.3027', '0.02592', '-0.0631', '-0.5796', '0.4001', '-0.32', '0.3298', '0.03674', '-0.0456', '0.755', '0.11365', '0.3528', '0.862', '0.7563', '-0.04312', '0.504', '1.113', '-0.3252', '-0.5146', '0.9463', '0.1617']",C61267,,C562606,,,,
mondo:0009740,neurofaciodigitorenal syndrome,"['neurofaciodigitorenal syndrome', 'Freire-Maia Pinheiro Opitz syndrome', 'Nfdr syndrome', 'Freire Maia-Pinheiro-Opitz syndrome']",,256690,2673,C0796088,,,,C537388,,,,
mondo:0009741,"neuroblastoma, susceptibility to, 1","['neuroblastoma, susceptibility to, 1, autosomal dominant, somatic mutation', 'susceptibility to neuroblastoma', 'neuroblastoma, susceptibility to']",,256700,635,C0027819,"['-0.0164', '0.03827', '0.01538', '0.0008616', '0.01845', '-0.05905', '0.04214', '0.04694', '-0.02484', '-0.02905', '-0.0053', '0.003254', '-0.00677', '0.027', '-0.02446', '-0.0269', '-0.004623', '-0.0443', '-0.0122', '-0.0895', '0.01469', '-0.03043', '0.04373', '-0.01167', '-0.006233', '-0.02216', '-0.01622', '0.02171', '-0.0236', '-0.0244', '0.05576', '-0.0261', '0.0727', '-0.00266', '0.02147', '-0.01217', '-0.0383', '0.0092', '0.002548', '-0.04742', '0.02649', '-0.0292', '0.04166', '-0.05127', '-0.01163', '-0.04977', '-0.01749', '0.0349', '0.0247', '0.02678', '-0.01671', '-0.02588', '0.0325', '0.00987', '-0.0195', '0.006157', '0.01944', '-0.02887', '-0.05722', '0.0059', '0.01695', '0.03806', '-0.00796', '0.02164', '0.00836', '0.04657', '0.06177', '0.0311', '-0.0442', '0.08606', '-0.01733', '-0.0054', '-0.004', '-0.04407', '0.0284', '0.04187', '-0.01286', '-0.0002499', '-0.00979', '-0.03833', '-0.02043', '-0.01559', '-0.014145', '0.05212', '-0.02829', '0.002176', '0.05527', '0.03165', '0.04767', '0.012344', '0.015434', '0.0348', '-0.01906', '0.011536', '0.1198', '0.04056', '0.0498', '-0.05276', '-0.03198', '0.004295']",,,,,,,
mondo:0009742,neuroectodermal melanolysosomal disease,"['Elejalde disease', 'neuroectodermal melanolysosomal disease', 'ELEJALDE disease']",,256710,33445,C1860157,"['-0.1351', '0.5', '0.05295', '0.2397', '-0.00851', '-0.3098', '-0.6343', '0.653', '0.2001', '0.2169', '-0.2754', '-0.446', '0.08496', '-0.02954', '0.1544', '0.2427', '-0.10016', '-0.1067', '-0.3088', '-0.0946', '-0.0682', '-0.03836', '0.4844', '-0.662', '0.2617', '-0.2935', '-0.3955', '0.1323', '-0.1693', '0.11255', '0.6875', '0.1405', '-0.2198', '-0.0685', '0.1697', '0.2446', '0.1693', '-0.0981', '0.1415', '0.02644', '0.5474', '-0.554', '-0.02983', '-0.6694', '-0.5386', '-0.3032', '-0.01412', '-0.393', '0.2396', '-0.2441', '-0.1649', '0.3323', '0.5425', '0.672', '-0.2605', '-0.04016', '0.8887', '-0.358', '-0.0829', '-0.0857', '-0.03967', '-0.5337', '0.1268', '0.4453', '-0.0963', '-0.2023', '0.35', '0.3538', '-0.493', '0.721', '-0.4922', '-0.1578', '-0.02885', '0.789', '-0.1614', '-0.1647', '-0.2903', '0.6475', '-0.1466', '-0.0889', '0.4932', '-0.676', '-0.2151', '0.433', '0.03442', '-0.4333', '0.2273', '0.839', '0.3748', '0.452', '0.2145', '0.4612', '-0.1219', '-0.0771', '0.07526', '0.541', '0.2998', '-1.013', '0.896', '0.2319']",,,C536203,,,,
mondo:0009743,"neurologic disease, infantile multisystem, with osseous fragility","['neurologic disease, infantile multisystem, with osseous fragility']",,256720,,C1850465,,,,C564954,,,,
mondo:0009744,neuronal ceroid lipofuscinosis 1,"['CLN1 variable age at onset', 'lipofuscin storage disease', 'ceroid storage disease', 'Santavuori disease', 'congenital NCL', 'infantile neuronal ceroid lipofuscinosis', 'congenital neuronal ceroid lipofuscinosis', 'classic late infantile CLN (type of CLN1)', 'CLN1', 'Santavuori-Haltia disease', 'ceroid lipofuscinosis, neuronal, type 1', 'ceroid lipofuscinosis, neuronal, 1', 'neuronal ceroid lipofuscinosis type 1', 'infantile CLN (type of CLN1)', 'juvenile CLN (type of CLN1)', 'PPT1 neuronal ceroid lipofuscinosis', 'CLN1 disease', 'neuronal ceroid lipofuscinosis 1 variable age of onset', 'ceroid lipofuscinosis, neuronal, 1, variable Age at onset', 'neuronal ceroid lipofuscinosis, infantile', 'ceroid lipofuscinosis neuronal 1', 'adult CLN (type of CLN1)', 'neuronal ceroid lipofuscinosis caused by mutation in PPT1']",0110721,256730,228329,,"['-0.31', '0.5063', '-0.0416', '-0.01595', '0.2379', '-0.4365', '-0.2291', '-0.148', '-0.3208', '-0.1874', '0.03256', '0.05716', '0.1564', '-0.2383', '0.155', '-0.08826', '-0.1036', '-0.2133', '-0.06085', '-0.5576', '0.1569', '-0.0972', '0.494', '-0.002438', '0.0453', '0.03574', '0.0896', '-0.0695', '-0.01883', '-0.1765', '0.1862', '0.1587', '0.2461', '0.009254', '0.1268', '-0.2115', '-0.08044', '-0.01973', '-0.347', '-0.5317', '0.00903', '-0.416', '0.1362', '0.10114', '-0.009285', '-0.4993', '0.06', '0.0797', '0.5356', '0.25', '0.04892', '0.08295', '-0.2014', '-0.1703', '0.0726', '-0.757', '0.471', '0.2037', '-0.3022', '0.2566', '0.2379', '0.1915', '0.3054', '-0.00861', '0.0572', '0.1552', '0.1564', '0.0372', '-0.4548', '0.004875', '-0.2262', '-0.1927', '0.0913', '0.2379', '0.263', '0.3435', '0.1545', '0.4783', '-0.3286', '-0.1455', '0.2092', '-0.1796', '-0.1244', '0.2045', '-0.09894', '-0.3198', '0.1677', '0.3196', '0.2878', '-0.1256', '0.2783', '0.014626', '-0.2039', '-0.2686', '0.602', '0.2173', '0.3066', '-0.307', '-0.1709', '0.07324']",C85861,,,,,,
mondo:0009745,neuronal ceroid lipofuscinosis 5,"['CLN5 disease, late infantile (subtype)', 'CLN5 disease', 'ceroid lipofuscinosis, neuronal, type 5', 'neuronal ceroid lipofuscinosis 5 variable age of onset', 'ceroid lipofuscinosis, neuronal, 5, variable Age at onset', 'CLN5 disease, juvenile', 'ceroid lipofuscinosis, neuronal, 5', 'neuronal ceroid lipofuscinosis Finnish variant', 'CLN5 neuronal ceroid lipofuscinosis', 'neuronal ceroid lipofuscinosis type 5', 'neuronal ceroid lipofuscinosis, late infantile, Finnish variant', 'Finnish Vlincl', 'neuronal ceroid lipofuscinosis caused by mutation in CLN5', 'CLN5 disease, adult', 'CLN5']",0110728,256731,228360,,"['0.148', '0.627', '-0.2496', '0.04892', '0.2375', '-1.155', '-0.007397', '0.2903', '-0.1958', '0.081', '-0.6343', '-0.034', '-0.10126', '0.07764', '0.4548', '-0.5024', '-0.2783', '-0.528', '0.1036', '-0.2134', '0.1659', '-0.3896', '-0.0982', '-0.2335', '0.08093', '-0.4146', '-0.42', '-0.362', '-0.8345', '0.4458', '1.063', '-0.2286', '0.539', '-0.3416', '0.6816', '0.09656', '-0.798', '0.4531', '-0.1986', '0.144', '-0.2812', '-0.3684', '0.965', '-0.08984', '0.1517', '-0.773', '-0.1696', '-0.01768', '0.06323', '0.2218', '0.6597', '0.402', '-0.8276', '-0.1316', '0.546', '-1.24', '0.7334', '-0.251', '-0.517', '-0.04257', '0.2695', '0.1122', '0.4065', '-0.02562', '0.4158', '-0.137', '0.6934', '-0.02803', '-0.1504', '0.4048', '-0.1294', '0.2133', '-0.1412', '-0.723', '0.4414', '0.3687', '0.1472', '0.1389', '-0.759', '-0.0345', '0.816', '0.2593', '-0.4954', '0.1804', '0.474', '-0.3818', '0.2137', '0.889', '-0.0738', '0.378', '-0.09717', '0.2727', '-0.532', '0.04358', '0.38', '0.008415', '0.635', '-0.262', '0.67', '-0.2083']",,,C575534,,,,
mondo:0009746,hereditary sensory and autonomic neuropathy type 4,"['HSAN4', 'congenital insensitivity to pain with anhidrosis', 'hereditary sensory neuropathy type 4', 'neuropathy, congenital sensory, with anhidrosis', 'HSNAN4', 'hereditary sensory and autonomic neuropathy 4', 'hereditary sensory and autonomic neuropathy caused by mutation in NTRK1', 'CIPA', 'CIP-anhidrosis syndrome', 'HSAN 4', 'congenital insensitivity to pain-anhidrosis syndrome', 'hereditary sensory neuropathy type IV', 'NTRK1 hereditary sensory and autonomic neuropathy', 'HSAN IV', 'insensitivity to pain, congenital, with anhidrosis', 'hereditary sensory and autonomic neuropathy type IV', 'familial dysautonomia, type 2']",0070146,256800,642,C0020074,"['0.6655', '0.10614', '-0.5576', '0.1997', '-0.2676', '-0.5923', '-0.09686', '0.996', '-0.4248', '0.1465', '-0.2395', '0.581', '0.1982', '0.333', '-0.3762', '0.8403', '0.1483', '0.4912', '-0.3667', '-0.939', '0.02132', '0.12396', '-0.3982', '0.4968', '-0.007275', '0.2903', '-0.552', '0.008385', '-0.0448', '-0.3064', '0.1632', '-0.3762', '-0.2512', '0.001718', '-0.858', '-0.3623', '0.2605', '-0.00792', '-0.1263', '0.1263', '-0.3333', '-0.0404', '-0.2086', '-0.0937', '0.3965', '-0.2664', '0.3237', '0.03958', '0.1938', '0.1171', '-0.3901', '1.002', '0.3855', '-0.3638', '0.1037', '0.7417', '0.2437', '-0.08685', '-0.05057', '-0.508', '0.537', '0.568', '0.321', '0.4995', '0.0682', '0.474', '-0.0246', '0.6826', '0.0511', '0.658', '-0.762', '0.3748', '-0.491', '0.1288', '0.5767', '0.3052', '0.4868', '0.1278', '-0.1127', '0.5117', '0.1665', '-0.4634', '0.4426', '0.1411', '-0.1859', '0.304', '0.1826', '0.2642', '0.4277', '-0.241', '0.2412', '0.3977', '0.4512', '-0.1032', '0.695', '0.641', '0.0921', '-0.2208', '0.6626', '0.2135']",C118633,,,,,,
mondo:0009747,mitochondrial DNA depletion syndrome 6 (hepatocerebral type),"['mitochondrial DNA depletion syndrome 6 (hepatocerebral type)', 'MPV17-related hepatocerebral mitochondrial DNA depletion syndrome', 'Navajo neuropathy', 'NN', 'Navajo familial neurogenic arthropathy', 'mitochondrial DNA depletion syndrome 6', 'Navajo neurohepatopathy', 'MTDPS6']",0080125,256810,255229,,"['-0.584', '0.0622', '-0.2213', '0.0907', '0.3198', '-0.86', '-0.00732', '0.2418', '-0.2742', '0.1754', '0.2257', '-0.2379', '0.02005', '0.2407', '-0.5537', '-0.0547', '0.1204', '0.01807', '-0.2488', '-0.747', '-0.02002', '-0.5063', '0.2034', '0.3008', '0.2095', '0.1151', '0.2059', '0.4307', '-0.303', '-0.4216', '0.02357', '0.4768', '0.4573', '0.1431', '-0.1891', '-0.282', '-0.5186', '-0.2238', '-0.2935', '0.349', '-0.3096', '-0.54', '0.2778', '0.568', '-0.279', '0.0802', '-0.5117', '-0.2366', '-0.132', '-0.00874', '-0.5317', '0.3066', '0.2512', '-0.2094', '0.08', '-0.0845', '0.3484', '-0.6733', '-0.2986', '-0.647', '0.3335', '0.1383', '0.06064', '0.3975', '-0.1317', '0.3472', '0.4944', '0.4668', '-0.3025', '0.518', '-0.3794', '0.01826', '0.1813', '0.3328', '0.1908', '-0.4968', '0.559', '0.3296', '0.1254', '0.09735', '0.011734', '-0.1774', '-0.2603', '0.3738', '-0.0541', '0.2389', '-0.156', '0.271', '0.2957', '-0.4446', '0.866', '-0.2039', '0.2202', '0.04004', '0.4165', '0.576', '0.3928', '-0.1295', '-0.2369', '0.6035']",,,C538344,,,,
mondo:0009748,hereditary sensory and autonomic neuropathy with spastic paraplegia,"['HSAN with spastic paraplegia', 'neuropathy, hereditary sensory, with spastic paraplegia, autosomal recessive']",,256840,139578,C4303565,"['0.774', '-0.1848', '-0.571', '0.718', '-0.1234', '-0.585', '-0.301', '0.679', '-0.517', '0.0501', '-0.10443', '0.4568', '0.02101', '0.559', '-0.2347', '0.1962', '-0.1642', '1.022', '-0.875', '-0.8286', '0.384', '-0.1257', '-0.9453', '0.1364', '0.0909', '-0.03537', '-0.8955', '0.07355', '-0.11957', '-0.4941', '0.797', '0.02614', '0.3113', '-0.1831', '-0.3076', '-0.5884', '0.3652', '0.07776', '0.1624', '-0.03934', '-0.6206', '-0.276', '-0.3608', '-0.5547', '0.661', '-0.595', '0.2186', '-0.063', '-0.1505', '0.04306', '-0.3506', '1.079', '0.3936', '-1.014', '0.10254', '0.6265', '0.902', '0.3423', '-0.251', '-0.2284', '0.5645', '0.6616', '0.2986', '0.2563', '-0.2295', '0.4087', '0.3174', '0.3406', '0.02019', '0.2837', '-0.8887', '0.3755', '-0.528', '-0.2668', '0.8564', '0.608', '-0.0733', '1.019', '-0.4731', '0.592', '-0.11804', '-0.505', '0.518', '0.4734', '0.4412', '0.02692', '0.511', '-0.01172', '0.3047', '-0.2957', '0.3154', '-0.02295', '0.6714', '-0.0543', '0.9976', '0.9575', '-0.28', '-0.3127', '0.0775', '0.1364']",,,C564948,,,,
mondo:0009749,giant axonal neuropathy 1,"['giant axonal neuropathy 1, autosomal recessive', 'neuropathy, giant axonal', 'giant axonal neuropathy caused by mutation in gan', 'GAN giant axonal neuropathy', 'GAN1', 'gan', 'giant axonal neuropathy-1', 'giant axonal neuropathy type 1', 'gan giant axonal neuropathy']",0090068,256850,643,C1850386,"['-0.4836', '0.01056', '-0.151', '0.0348', '-0.1182', '-0.437', '0.2006', '0.896', '-0.536', '-0.539', '0.07574', '0.2522', '-0.03967', '0.013664', '0.2935', '0.08575', '0.3333', '-0.3198', '0.0618', '-0.3403', '-0.278', '-0.279', '-0.186', '0.1571', '-0.5874', '-0.1792', '0.2844', '0.251', '-0.3477', '-0.4202', '0.4844', '-0.0833', '0.523', '-0.09204', '-0.02031', '-0.4578', '-0.1891', '-0.01569', '-0.262', '-0.2076', '0.02751', '-0.1449', '0.3604', '0.2988', '0.2605', '-0.3022', '0.1654', '-0.261', '-0.4832', '-0.3613', '0.084', '0.3982', '-0.2145', '-0.547', '-0.01301', '-0.0659', '0.065', '-0.4731', '0.0398', '-0.2378', '-0.2219', '0.2194', '0.2286', '0.4097', '-0.5005', '0.8286', '0.4038', '0.8228', '-0.1085', '-0.1265', '-0.535', '-0.03687', '0.0914', '0.2988', '0.641', '0.24', '0.1958', '0.2318', '0.00651', '-0.3206', '0.09424', '-0.341', '-0.01674', '1.115', '-0.02434', '0.4521', '-0.04517', '-0.1148', '0.2262', '-0.0753', '0.362', '0.1079', '0.1226', '-0.1516', '0.8223', '0.1436', '0.3958', '0.05966', '0.2224', '-0.2686']",,,,,,,
mondo:0009750,"neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive","['Charcot-Marie-Tooth disease with excessive myelin folding, autosomal recessive', 'neuropathy, hereditary motor and sensory, with excessive myelin folding complex, autosomal recessive', 'HMSN with excessive myelin Outfolding, autosomal recessive']",,256855,,C1850385,,,,C564947,,,,
mondo:0009751,"neuropathy, hereditary sensory, atypical","['neuropathy, hereditary sensory, atypical', 'atypical hereditary sensory neuropathy']",0070160,256860,,C1850384,,,,C564946,,,,
mondo:0009752,"neuropathy, painful","['neuropathy, painful']",,256870,,C1850383,,,,C564945,,,,
mondo:0009754,"neutropenia, lethal congenital, with eosinophilia","['neutropenia, lethal congenital, with eosinophilia', 'lethal congenital neutropenia with eosinophilia', 'neutropenia lethal congenital with eosinophilia']",,257100,,C1850381,,,,C564943,,,,
mondo:0009755,neutrophil actin dysfunction,"['Clark Nevus', 'Clark^s Nevus', 'dysplastic Nevus', 'dysplastic nevi', 'NAD', 'Nevus with architectural disorder and cytologic atypia of melanocytes', 'Nevus with architectural disorder', 'Atypical Nevus', 'lentiginous Nevus', 'dysplastic nevus', 'neutrophil actin dysfunction']",,257150,625,C1850380,,C3694,,C564942,,,,
mondo:0009756,Niemann-Pick disease type A,"['Niemann-Pick disease, Intermediate, protracted neurovisceral', 'sphingomyelin lipidosis', 'sphingomyelinase deficiency', 'Niemann-PICK disease, type A']",0070111,257200,77292,C0268242,"['0.1456', '0.855', '-0.11646', '0.2947', '0.6196', '-0.9746', '-0.4392', '0.8687', '-0.6104', '-0.4155', '-0.05957', '-0.5186', '-0.0839', '0.5396', '-0.3955', '0.0743', '-0.08624', '-0.0974', '-0.9287', '-0.9033', '-0.4292', '-0.623', '0.6514', '0.03366', '-0.00596', '-0.07367', '0.191', '-0.00746', '-0.3909', '0.1531', '0.9307', '-0.0616', '0.685', '-0.602', '-0.2136', '0.09216', '-0.7915', '0.0919', '-0.0397', '-0.09094', '-0.4392', '-0.2246', '0.00010985', '0.2163', '-0.6353', '0.03885', '-0.331', '-0.5513', '0.1938', '0.2098', '0.02472', '-0.1893', '0.2019', '-0.588', '-0.00994', '-0.4695', '-0.657', '0.792', '-0.2172', '-0.4365', '-0.0923', '0.0513', '0.885', '-0.09106', '0.01653', '-0.09766', '0.5796', '0.03635', '-0.685', '-0.00977', '-0.6216', '-0.395', '-0.7183', '0.11536', '0.8755', '-0.4524', '-0.003567', '0.141', '-0.2632', '0.1648', '0.001829', '-1.066', '-0.3174', '-0.0667', '-0.1777', '-0.1815', '0.7524', '-0.05615', '1.124', '0.2632', '-0.007812', '0.5874', '-0.2942', '0.308', '-0.11115', '0.2208', '-0.3125', '-0.1278', '0.7026', '-0.2583']",C126561,,D052536,,,,
mondo:0009757,"Niemann-Pick disease, type C1","['neurovisceral storage disease with vertical supranuclear ophthalmoplegia', 'NPC1', 'Niemann-Pick disease type C1', 'Niemann-Pick disease, type C', 'Niemann-Pick disease, type D', 'Niemann-Pick disease without sphingomyelinase deficiency', 'Niemann-Pick disease with cholesterol esterification block', 'Niemann-Pick disease, chronic neuronopathic form', 'Niemann-PICK disease, type C1', 'Niemann-Pick disease, subacute juvenile form', 'type C1 Niemann-Pick disease', 'Niemann-Pick disease, type C1', 'Niemann-Pick disease, nova Scotian type']",0070113,257220,,C3179455,,C126864,,,,,,
mondo:0009758,congenital stationary night blindness 1B,"['night blindness, congenital stationary, type 1B', 'GRM6 congenital stationary night blindness', 'congenital stationary night blindness 1B autosomal recessive', 'CSNB1B', 'autosomal recessive complete congenital stationary night blindness', 'congenital stationary night blindness caused by mutation in GRM6', 'CSNB, complete, autosomal recessive', 'night blindness, congenital stationary (complete), 1B, autosomal recessive', 'night blindness, congenital stationary, complete, autosomal recessive', 'congenital stationary night blindness type 1B']",0110865,257270,,C1850362,,,,,,,,
mondo:0009759,mosaic variegated aneuploidy syndrome 1,"['MVA1', 'Mosaic variegated aneuploidy syndrome type 1', 'mosaic variegated aneuploidy syndrome type 1', 'BUB1B mosaic variegated aneuploidy syndrome', 'mosaic variegated aneuploidy syndrome 1', 'MVA syndrome', 'mosaic variegated aneuploidy syndrome caused by mutation in BUB1B', 'MOSAIC variegated aneuploidy syndrome 1']",0080141,257300,,CN031748,,,,,,,,
mondo:0009760,Norman-Roberts syndrome,"['Norman-Roberts syndrome', 'lissencephaly 2 (Norman-Roberts type)', 'LIS2', 'lissencephaly syndrome, Norman-Roberts type', 'Microlissencephaly type A', 'lissencephaly syndrome Norman-Roberts type', 'lissencephaly 2', 'Norman Roberts lissencephaly syndrome']",0060902,257320,89844,C0796089,"['-0.1884', '0.2249', '0.3926', '-0.598', '0.0811', '-0.1503', '0.258', '0.4446', '-0.9414', '-0.0734', '-0.3508', '-0.1068', '0.1869', '-0.462', '-0.1638', '-0.215', '0.874', '-0.1102', '-0.2363', '-0.528', '0.1909', '-0.01978', '0.57', '-0.0772', '0.05237', '-0.01587', '-0.1464', '0.03357', '0.2263', '0.01627', '0.2666', '0.1274', '0.3691', '0.076', '0.1592', '0.011375', '-0.1072', '-0.03513', '-0.2343', '-0.4636', '0.419', '-0.4946', '-0.2969', '-0.07544', '-0.3772', '-0.4026', '0.2942', '0.2988', '-0.006927', '-0.2247', '0.161', '-0.05286', '-0.2004', '-0.2477', '-0.4053', '0.0156', '0.010475', '0.04572', '-0.1001', '0.2993', '-0.404', '0.00998', '-0.1237', '-0.02031', '-0.1307', '0.04062', '0.246', '0.3176', '-0.542', '0.3188', '-0.5', '0.3372', '0.4412', '-0.0001625', '-0.377', '0.33', '0.262', '-0.3625', '-0.2532', '-0.1037', '0.002588', '-0.02681', '-0.4648', '0.509', '-0.1512', '-0.0456', '-0.04776', '0.6016', '0.4695', '0.0812', '0.111', '0.466', '0.3752', '-0.1344', '0.2883', '0.089', '0.2727', '-0.3628', '0.4768', '0.3047']",,,,,,,
mondo:0009761,cystic hygroma,"['cystic hygroma, fetal', 'nuchal bleb, familial', 'cystic hygroma, foetal', 'cystic hygroma', 'cystic lymphangioma', 'hygroma', 'macrocystic lymphatic malformation']",3081,257350,79486,,,C3724,1000888,D018191,,,10058949,
mondo:0009762,"nystagmus, congenital, autosomal recessive","['nystagmus, congenital, autosomal recessive', 'Nystagmus, congenital motor, autosomal recessive']",0111797,257400,,C3151571,,,,C564938,,,,
mondo:0009763,obesity-hypoventilation syndrome,"['obesity-hypoventilation syndrome', 'Pickwickian syndrome']",,257500,,C0031880,,,,D010845,786.09,,,
mondo:0009764,"ocular motor apraxia, Cogan type","['COMA', 'ocular motor apraxia', 'oculomotor apraxia, Cogan type', 'oculomotor apraxia Cogan type', 'saccade initiation failure, congenital', 'congenital oculomotor apraxia', 'saccade initiation failure congenital', 'Cogan^s syndrome type 2', 'oculomotor apraxia, congenital, Cogan-type']",0080849,257550,1125,,,,,C537423,,,,
mondo:0009765,ocular myopathy with curare sensitivity,['ocular myopathy with curare sensitivity'],,257600,,C1850341,,,,C564937,,,,
mondo:0009766,oculocerebral hypopigmentation syndrome of Preus,"['oculocerebral hypopigmentation syndrome of Preus', 'oculocerebral hypopigmentation syndrome type Preus']",,257790,2720,C2931646,,,,C537866,,,,
mondo:0009767,"oculocerebral hypopigmentation syndrome, Cross type","['Kramer syndrome', 'Cross syndrome', 'oculocerebral syndrome with hypopigmentation', 'hypopigmentation oculocerebral syndrome Cross type', 'oculocerebral hypopigmentation syndrome']",,257800,2719,,,,,,759.89,E70.3,,
mondo:0009768,"oculodentodigital dysplasia, autosomal recessive","['oculodentoosseous dysplasia, autosomal recessive', 'ODOD recessive', 'oculodentodigital dysplasia, autosomal recessive', 'oculodentoosseous dysplasia recessive', 'autosomal recessive oculodentodigital dysplasia', 'ODOD, autosomal recessive', 'ODDD, autosomal recessive']",,257850,,C2749477,,,,C567605,,,,
mondo:0009769,oculo-palato-cerebral syndrome,"['oculopalatocerebral syndrome', 'oculo-palato-cerebral dwarfism', 'OPC dwarfism', 'oculopalatocerebral dwarfism']",,257910,2714,C1850338,,,,C564935,,,,
mondo:0009770,3MC syndrome 1,"['Michels syndrome, formerly', 'craniosynostosis with 51D anomalies', '3MC1', '3MC syndrome caused by mutation in MASP1', '3Mc syndrome type 1', 'oculopalatoskeletal syndrome', '3MC syndrome 1', 'MASP1 3MC syndrome', '3MC syndrome type 1', 'Michels syndrome']",0060575,257920,2506,C0796059,"['-0.2856', '0.11816', '0.314', '-0.2454', '0.0611', '-0.2168', '0.02979', '0.2329', '-0.4175', '-0.2019', '-0.116', '-0.1686', '0.12006', '-0.02151', '-0.1213', '-0.1418', '0.04282', '-0.1392', '-0.11035', '-0.2544', '0.2715', '0.010635', '0.05743', '-0.111', '0.2534', '0.0467', '-0.04105', '0.138', '0.3628', '-0.05103', '0.0795', '0.1036', '0.2874', '0.1511', '0.1683', '-0.1228', '0.1168', '-0.1859', '-0.0812', '-0.2834', '0.2605', '-0.1539', '0.0808', '-0.00248', '-0.2313', '-0.3333', '0.2103', '0.2366', '-0.06', '-0.0634', '-0.2922', '-0.01346', '-0.04205', '-0.114', '-0.1335', '-0.419', '0.3179', '-0.0643', '-0.1805', '0.1146', '0.09894', '0.03802', '0.01984', '0.161', '-0.04208', '0.0402', '0.1858', '0.0736', '-0.251', '0.06223', '-0.3027', '0.2136', '0.1831', '-0.2145', '-0.09674', '-0.04968', '0.1713', '-0.2367', '-0.279', '0.002249', '0.0894', '-0.02237', '-0.11884', '0.3838', '-0.1864', '-0.2576', '0.12396', '0.5396', '0.1231', '0.3433', '0.04993', '0.2046', '0.279', '-0.06915', '0.678', '-0.09894', '0.305', '-0.3838', '0.2395', '0.07684']",,1001978,,,,,
mondo:0009771,oculotrichodysplasia,"['Cecato de Lima-Pinheiro syndrome', 'OTD', 'oculotrichodysplasia']",,257960,2718,C1850332,,,,C564934,,,,
mondo:0009772,oculorenocerebellar syndrome,"['absence of the cerebellar granular layer, mental retardation, tapetoretinal degeneration and progressive glomerulopathy', 'absence of the cerebellar granular layer, intellectual disability, tapetoretinal degeneration and progressive glomerulopathy', 'oculorenocerebellar syndrome', 'ORC syndrome']",,257970,2715,C1850331,,,,C537739,,,,
mondo:0009773,odonto-onycho-dermal dysplasia,"['ectodermal dysplasia', 'odontoonychodermal dysplasia', 'OODD']",,257980,2721,C0796093,"['-0.11847', '0.2391', '0.2842', '-0.3767', '0.3193', '-0.17', '0.141', '0.02922', '0.02304', '-0.2303', '-0.09393', '-0.2527', '-0.6733', '-0.1616', '-0.2998', '0.2252', '0.5366', '-0.1597', '-0.4277', '-0.694', '-0.1752', '0.0983', '0.508', '-0.1044', '-0.01008', '0.2554', '-0.3896', '-0.00737', '0.1793', '-0.5415', '0.11523', '-0.01755', '-0.2805', '0.06635', '0.679', '0.2137', '-0.2032', '-0.02702', '-0.12256', '-0.396', '0.2747', '-0.3313', '-0.2057', '-0.2203', '-0.02849', '-0.2769', '0.0989', '0.3716', '0.3', '-0.2754', '-0.007698', '0.4446', '0.1254', '0.2537', '-0.6924', '-0.0756', '0.319', '-0.438', '-0.536', '-0.2798', '0.3513', '-0.1542', '-0.2783', '-0.2335', '0.1935', '0.1808', '0.2742', '0.341', '0.01217', '0.425', '-0.599', '-0.3054', '0.3723', '-0.001336', '0.0392', '-0.04276', '0.3406', '-0.003122', '-0.1617', '0.06586', '0.053', '-0.1196', '-0.0692', '0.0724', '0.1221', '-0.1615', '-0.4268', '0.4917', '0.4255', '0.3313', '0.0903', '0.2195', '0.3726', '0.5737', '0.6543', '-0.1323', '0.306', '-0.572', '0.244', '0.5884']",,,C537742,,,,
mondo:0009774,cloacal exstrophy,"['OEIS complex', 'omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects complex', 'OEIS syndrome', 'cloacal exstrophy sequence', 'omphalocele - cloacal exstrophy - imperforate anus - spinal defect', 'omphalocele-exstrophy-imperforate anus-spinal defects', 'omphalocele-cloacal exstrophy-imperforate anus-spinal defect syndrome', 'omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects', 'cloacal exstrophy (disease)', 'cloacal exstrophy']",0080175,,93929,C0345217,,,,C537748,759.89,,10067424,0010475
mondo:0009775,Oguchi disease-1,"['Oguchi disease type 1', 'SAG Oguchi disease', 'congenital stationary night blindness Oguchi type 1', 'night blindness, congenital stationary, Oguchi type 1', 'CSNBO1', 'Oguchi disease 1', 'Oguchi disease caused by mutation in SAG']",0110712,258100,,,,,,,,,,
mondo:0009776,spermatogenic failure 1,"['spermatogenic failure 1', 'Oligosynaptic infertility', 'Oligochiasmatic infertility', 'SPGF1']",0070188,258150,217034,C0403810,,,,C562902,,,,
mondo:0009777,Oliver syndrome,"['Oliver syndrome', 'postaxial polydactyly-intellectual disability syndrome', 'postaxial polydactyly and mental retardation', 'postaxial polydactyly and intellectual disability']",,258200,2920,C1850320,,,,C564931,,,,
mondo:0009778,"olivopontocerebellar atrophy II, autosomal recessive","['olivopontocerebellar atrophy II, autosomal recessive', 'OPCA II, Fickler-Winkler type']",,258300,,C1850319,,,,C564930,,,,
mondo:0009779,autosomal recessive omodysplasia,"['micromelic dysplasia congenita with dislocation of radius', 'omodysplasia, generalised form', 'micromelic dysplasia, congenital, with dislocation of radius', 'omodysplasia generalized form', 'micromelic dysplasia-dislocation of radius syndrome', 'omodysplasia autosomal recessive', 'omodysplasia generalised form', 'omodysplasia, autosomal recessive', 'omodysplasia, generalized form', 'omodysplasia type 1', 'omodysplasia 1', 'OMOD1']",0080844,258315,93329,C1850318,"['-0.2465', '0.4111', '0.1978', '-0.3625', '0.2458', '-0.348', '-0.03433', '0.2751', '-0.3691', '-0.2189', '-0.2108', '0.0631', '0.0453', '0.05914', '0.158', '0.1487', '0.2407', '0.0059', '-0.296', '-0.4277', '-0.3096', '0.103', '0.4487', '-0.04578', '-0.01674', '0.2964', '0.01275', '-0.2305', '0.2637', '-0.1909', '-0.002718', '0.1207', '0.05884', '0.0346', '0.1296', '-0.001864', '-0.04794', '-0.236', '-0.0598', '-0.2812', '-0.1698', '-0.6504', '-0.1094', '0.1214', '-0.1613', '-0.2856', '-0.3174', '0.2454', '0.1559', '-0.05878', '0.1198', '-0.08545', '-0.0694', '-0.02281', '-0.2546', '-0.6914', '0.1194', '-0.1677', '-0.10474', '-0.07947', '0.2238', '-0.07886', '-0.0158', '0.2362', '-0.1213', '-0.1317', '0.11957', '0.1381', '-0.128', '0.176', '-0.3855', '-0.08777', '0.2286', '-0.189', '0.0957', '0.3555', '-0.09326', '0.0988', '-0.0984', '-0.1769', '-0.06775', '0.1505', '0.2435', '0.3', '0.1043', '0.3284', '0.03476', '0.316', '0.1862', '0.1571', '-0.0494', '0.168', '0.04657', '0.2058', '0.5957', '0.2944', '0.551', '-0.423', '0.0835', '0.1749']",,,,,,,
mondo:0009780,lethal omphalocele-cleft palate syndrome,"['omphalocele cleft palate syndrome lethal', 'Czeizel syndrome', 'cleft palate-omphalocele syndrome, lethal', 'omphalocele-cleft palate syndrome, lethal']",,258320,2736,C1850317,,,,C537747,,,,
mondo:0009781,Onychotrichodysplasia and neutropenia,"['onycho-tricho-dysplasia-neutropenia syndrome', 'Onychotrichodysplasia and neutropenia']",,258360,2739,C1850316,,,,C537752,,,,
mondo:0009782,ophthalmoplegia totalis with ptosis and miosis,['ophthalmoplegia totalis with ptosis and miosis'],,258400,,C1850314,,,,C564927,,,,
mondo:0009783,"progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1","['POLG autosomal recessive progressive external ophthalmoplegia', 'progressive external ophthalmoplegia, autosomal recessive 1', 'cerebellar ataxia infantile with progressive external ophthalmoplegia', 'arPEO', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive type 1', 'PEOB1', 'autosomal recessive progressive external ophthalmoplegia caused by mutation in POLG', 'autosomal recessive progressive external ophthalmoplegia', 'progressive external ophthalmoplegia with cerebellar ataxia infantile', 'progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal recessive 1']",0111522,258450,,C4225153,,,,,,,,
mondo:0009784,ophthalmoplegic neuromuscular disorder with abnormal mitochondria,['ophthalmoplegic neuromuscular disorder with abnormal mitochondria'],,258470,,C1850302,,,,C564925,,,,
mondo:0009785,opsismodysplasia,"['OPSISMODYSPLASIA', 'OPSMD', 'opsismodysplasia']",,258480,2746,C0432219,"['-0.4446', '0.1915', '0.2028', '-0.4602', '0.34', '-0.422', '0.0638', '0.7627', '-0.521', '-0.2888', '-0.02376', '0.3733', '0.2764', '-0.3599', '-0.2131', '0.5093', '0.575', '0.03087', '-0.5396', '-0.2969', '-0.1279', '0.02753', '0.6064', '-0.1001', '-0.06024', '-0.1968', '-0.05597', '-0.199', '0.4287', '-0.2815', '0.0853', '-0.1181', '0.2905', '0.2234', '0.2524', '0.01689', '-0.2194', '-0.3237', '-0.1332', '-0.0809', '-0.2468', '-0.2913', '-0.0223', '-0.2045', '-0.1713', '-0.1918', '-0.122', '0.807', '-0.3809', '-0.2776', '-0.4185', '-0.1299', '-0.269', '0.2668', '-0.1121', '-0.4246', '-0.10126', '-0.1642', '0.324', '0.1273', '0.297', '0.2288', '-0.6094', '0.2576', '0.1364', '-0.1882', '0.05786', '0.4602', '-0.521', '0.4307', '-0.03967', '0.1769', '0.2335', '-0.0637', '-0.335', '0.1976', '0.02724', '-0.12195', '-0.1953', '0.02081', '0.00997', '0.11414', '0.1934', '0.4727', '0.0586', '0.4104', '-0.1787', '0.227', '0.4575', '-0.02788', '0.0988', '0.1996', '0.1613', '0.11017', '0.807', '0.469', '0.382', '-0.4568', '0.3909', '-0.008965']",,,C537122,,,,
mondo:0009786,optic atrophy 6,"['optic atrophy 6', 'OPA6', 'optic atrophy, congenital or early infantile, autosomal recessive']",0111435,258500,99012,,,,,C537127,,,,
mondo:0009787,3-methylglutaconic aciduria type 3,"['MGA type III', '3-methylglutaconic aciduria, type 3', 'optic atrophy 3, autosomal recessive', 'OPA3, autosomal recessive', 'MGA, type 3', 'MGA3', 'MGCA3', 'autosomal recessive optic atrophy plus syndrome', 'Costeff syndrome', '3-methylglutaconic aciduria caused by mutation in OPA3', 'infantile optic atrophy with chorea and spastic paraplegia', 'optic atrophy, infantile, with chorea and spastic paraplegia', 'OPA3 defect', 'optic atrophy infantile with chorea and spastic paraplegia', 'Iraqi-Jewish optic atrophy plus', '3-methylglutaconic aciduria type III', 'autosomal recessive optic atrophy type 3', 'Costeff optic atrophy syndrome', 'Iraqi Jewish optic atrophy plus', 'optic atrophy plus syndrome', '3-alpha methylglutaconic aciduria type III', 'Iraqi-Jewish ^optic atrophy plus^', '3-methylglutaconic aciduria, type III', 'OPA3 3-methylglutaconic aciduria']",0110004,258501,67047,C0574084,"['-0.2094', '0.4587', '-0.3953', '-0.0356', '-0.1434', '-0.3823', '0.17', '0.5195', '-0.7646', '0.005875', '-0.3232', '0.08984', '0.1119', '-0.1377', '0.288', '-0.2024', '0.0959', '-0.376', '-0.3', '-0.6533', '-0.1826', '-0.317', '0.11237', '-0.1539', '-0.05518', '0.10645', '-0.03333', '0.2308', '-0.4685', '0.143', '0.4148', '0.3071', '0.2751', '0.1957', '-0.2617', '0.07825', '-0.1652', '-0.3457', '-0.3806', '0.3713', '0.115', '-0.4136', '0.2052', '-0.0534', '-0.2146', '-0.00796', '-0.04398', '-0.0847', '-0.1178', '-0.328', '-0.2257', '0.10913', '-0.1936', '-0.4033', '0.547', '0.1403', '0.7764', '-0.263', '-0.1456', '0.3928', '0.0342', '0.04944', '0.5166', '0.04385', '-0.5854', '0.1766', '0.6113', '0.369', '-0.04724', '0.4294', '-0.2072', '0.1233', '-0.3362', '-0.2634', '0.5786', '0.185', '-0.04965', '-0.1057', '0.0341', '-0.263', '0.6245', '-0.10095', '0.01808', '0.625', '-0.1902', '0.1298', '-0.1282', '0.3242', '0.2084', '-0.11676', '0.1912', '0.12134', '0.0647', '-0.171', '0.3555', '-0.02321', '0.531', '-0.2537', '0.1335', '0.04272']",,,C535311,,,,
mondo:0009788,"optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive","['optic atrophy, hearing loss, and peripheral neuropathy, autosomal recessive']",,258650,,C1839566,,,,,,,,
mondo:0009789,"nonarteritic anterior ischemic optic neuropathy, susceptibility to","['optic neuropathy, anterior ischemic, susceptibility to', 'nonarteritic anterior ischemic optic neuropathy, susceptibility to', 'Naion, susceptibility to', 'susceptibility to nonarteritic anterior ischemic optic neuropathy', 'susceptibility to nonarteritic anterior ischaemic optic neuropathy']",,258660,,,,,,,,,,
mondo:0009790,Opticocochleodentate degeneration,['Opticocochleodentate degeneration'],,258700,,C0520711,,,,C563002,333.90,,,
mondo:0009791,"oral sensibility, disturbance of","['disturbance of oral sensitivity', 'oral sensibility, disturbance of', 'impairment of oral perception']",,258800,,,,,,,,,,
mondo:0009792,ichthyosis-oral and digital anomalies syndrome,"['Clayton Smith-Donnai syndrome', 'unusual facies, digital abnormalities, and ichthyosis', 'oral and digital anomalies with ichthyosis', 'ichthyosis tapered fingers midline groove up']",,258840,2272,C1850268,,,,C536272,,,,
mondo:0009793,orofaciodigital syndrome III,"['oral-Facial-digital syndrome, type 3', 'oral-facial-digital syndrome type 3', 'Ofds 3', 'oral facial digital syndrome 3', 'oral facial digital syndrome type 3', 'orofaciodigital syndrome III', 'orofaciodigital syndrome type 3', 'OFD3', 'OFD syndrome 3', 'orofaciodigital syndrome 3', 'Sugarman syndrome', 'orofaciodigital syndrome type III']",0060373,258850,2752,,,,,C557817,,,,
mondo:0009794,orofaciodigital syndrome IV,"['Baraitser-Burn syndrome', 'oral facial digital syndrome 4', 'Ofd syndrome with tibial defects', 'oral-Facial-digital syndrome, type 4', 'Ofd syndrome, Baraitser-Burn type', 'OFD syndrome 4', 'orofaciodigital syndrome 4', 'OFD4', 'Ofds 4', 'orofaciodigital syndrome type 4', 'orofaciodigital syndrome type IV', 'oral facial digital syndrome type 4', 'Mohr-Majewski syndrome', 'orofaciodigital syndrome IV', 'oral-facial-digital syndrome type 4', 'orofaciodigital syndrome with tibial dysplasia']",0060374,258860,2753,C0406727,"['-0.1398', '0.1681', '0.2344', '-0.278', '0.2446', '-0.508', '-0.02962', '0.5796', '-0.5884', '-0.339', '-0.2405', '0.00929', '-0.0514', '-0.3267', '-0.2079', '0.2878', '0.595', '-0.2493', '-0.1714', '-0.1304', '-0.11615', '0.2101', '0.2075', '-0.3276', '0.02332', '0.1842', '-0.2546', '0.00855', '0.699', '-0.2279', '0.05112', '-0.3572', '0.1528', '0.344', '0.5205', '-0.4966', '-0.1041', '-0.305', '-0.1295', '-0.05695', '-0.2603', '-0.3396', '-0.2822', '-0.141', '-0.2196', '-0.314', '-0.147', '0.7715', '-0.2411', '-0.362', '-0.2408', '0.01733', '-0.456', '-0.1377', '-0.6045', '-0.4175', '-0.014854', '-0.343', '-0.06665', '0.04236', '0.1914', '0.2004', '-0.534', '0.1193', '-0.4578', '-0.0969', '-0.1241', '0.3958', '-0.3215', '0.2695', '-0.5347', '0.3005', '0.275', '-0.3293', '0.1387', '0.4937', '-0.1475', '-0.2255', '-0.3228', '-0.2761', '0.3577', '0.1377', '0.299', '0.582', '0.00345', '0.0692', '-0.1613', '0.7583', '0.06824', '0.1027', '0.03903', '0.1271', '0.4304', '0.03488', '0.935', '0.062', '0.4507', '-0.927', '0.0366', '0.4148']",,,C537133,,,,
mondo:0009795,orofaciodigital syndrome IX,"['oral-Facial-digital syndrome with retinal abnormalities', 'orofaciodigital syndrome type IX', 'orofaciodigital syndrome 9', 'orofaciodigital syndrome type 9', 'OFD9', 'orofaciodigital syndrome with retinal abnormalities', 'Ofds 9', 'OFD syndrome 9', 'oral facial digital syndrome type 9', 'oral-Facial-digital syndrome, type 9', 'oral facial digital syndrome 9', 'oral-facial-digital syndrome with retinal abnormalities', 'orofaciodigital syndrome IX', 'oral-facial-digital syndrome type 9']",0060382,258865,141007,C0796102,,,,C557818,,,,
mondo:0009796,ornithine aminotransferase deficiency,"['gyrate atrophy of choroid and retina with or without ornithinemia', 'gyrate atrophy of choroid and retina', 'Girate atrophy of the retina', 'hyperornithinemia', 'gyrate atrophy', 'gyrate atrophy of the retina', 'hoga', 'Fuchs gyrate atrophy', 'Fuchs gyrate atrophy of the choroid and retina', 'hyperornithinemia with gyrate atrophy of choroid and retina', 'Ornithinemia', 'Okt deficiency', 'ornithine Keto acid aminotransferase deficiency', 'GACR', 'Fuchs atrophia gyrata chorioideae et retinae', 'gyrate atrophy of the choroid and/or retina', 'ornithine-Delta-aminotransferase deficiency', 'ornithine aminotransferase deficiency', 'ornithine ketoacid aminotransferase deficiency', 'OKT deficiency', 'Oat deficiency', 'hyperornithinemia-gyrate atrophy of choroid and retina syndrome', 'Ornithinemia with gyrate atrophy', 'OAT deficiency']",1415,258870,414,C0018425,"['-0.2305', '0.1984', '-0.4866', '0.521', '-0.1407', '-0.4163', '-0.2245', '0.578', '-0.2683', '-0.407', '-0.362', '-0.1299', '-0.2019', '0.1294', '-0.1815', '-0.3438', '-0.074', '-0.3423', '0.288', '-0.3179', '-0.1376', '-0.3015', '-0.144', '0.2507', '-0.1059', '0.4343', '-0.2078', '0.3079', '-0.592', '0.3132', '1.239', '-0.2883', '-0.1289', '0.05817', '-0.0695', '0.1359', '0.02362', '-0.4758', '0.3804', '-0.02449', '0.003464', '-0.4983', '0.7344', '-0.32', '-0.3396', '-0.0858', '0.3574', '-0.3145', '-0.264', '-0.2698', '0.3904', '0.1433', '0.3623', '-0.6387', '0.199', '-0.03778', '1.166', '-0.1501', '-0.5513', '-0.2434', '0.3865', '-0.1119', '0.08484', '-0.01025', '-0.2576', '0.598', '0.7314', '0.6597', '0.1686', '0.1317', '0.409', '0.1116', '0.04926', '0.01582', '0.6514', '0.4634', '-0.06094', '-0.5845', '-0.1498', '-0.4878', '0.2766', '-0.03012', '0.1346', '1.289', '-0.01582', '0.2446', '-0.3125', '-0.0164', '0.4507', '-0.0853', '0.5234', '0.2917', '0.0687', '0.0657', '0.2241', '-0.3066', '0.6553', '-0.1196', '0.2278', '-0.0971']",C84744,,D015799,,,,
mondo:0009797,orotic aciduria,"['OPRT and ODC deficiency', 'orotic aciduria type 1', 'Umps deficiency', 'orotic aciduria without megaloblastic Anemia', 'orotidylic pyrophosphorylase and orotidylic decarboxylase deficiency', 'orotate phosphoribosyltransferase and OMP decarboxylase deficiency', 'oroticaciduria', 'orotic aciduria', 'uridine monophosphate synthase deficiency', 'orotic aciduria II (formerly)', 'oroticaciduria 1', 'Ump synthase deficiency', 'UMP synthtase deficiency', 'hereditary orotic aciduria', 'orotic aciduria 1', 'orotic aciduria without megaloblastic Anaemia', 'uridine monophosphate synthetase deficiency', 'orotate phosphoribosyltransferase and orotidylic decarboxylase deficiency', 'UMPS', 'orotidylic decarboxylase deficiency']",0050833,258900,30,,"['-0.4304', '0.2461', '0.162', '-0.472', '0.1946', '-0.3943', '-0.4993', '0.3035', '-0.2382', '-0.10046', '-0.419', '-0.0005455', '0.1522', '-0.02202', '-0.4294', '0.07605', '0.09717', '-0.2869', '-0.638', '-0.713', '0.236', '-0.4219', '0.2124', '-0.10535', '0.1611', '0.03647', '0.1525', '-0.007', '-0.03598', '-0.0872', '0.1968', '-0.01935', '0.3308', '0.522', '-0.5093', '-0.2817', '-0.268', '-0.1765', '-0.1921', '-0.2954', '-0.275', '-0.385', '0.4148', '-0.07367', '-0.3323', '-0.6665', '0.3457', '-0.1261', '0.2173', '0.3284', '-0.0892', '0.1293', '-0.1827', '-0.1305', '0.195', '-0.3904', '0.4033', '-0.002806', '-0.6177', '0.38', '0.069', '-0.152', '0.2329', '-0.4705', '0.4922', '-0.0759', '0.424', '0.3147', '-0.4604', '0.1472', '-0.359', '0.1074', '-0.3232', '0.1886', '0.186', '0.3428', '0.2854', '0.0001343', '0.128', '0.03882', '0.256', '0.1384', '0.1439', '0.0971', '0.4111', '0.206', '0.1642', '0.2229', '0.3142', '0.1736', '0.4678', '0.463', '-0.2676', '-0.491', '0.4548', '0.9795', '0.255', '-0.2925', '0.2073', '0.1436']",C98944,,,,,10052621,
mondo:0009798,Primrose syndrome,"['PRIMS', 'intellectual disability-cataracts-calcified pinnae-myopathy syndrome', 'Primrose syndrome', 'ossified EAR cartilages with mental deficiency, muscle wasting, and BONY changes']",,259050,3042,C0796121,"['-0.1754', '-0.1726', '0.5806', '0.616', '0.1835', '0.658', '-0.3445', '0.9355', '-0.3577', '-0.75', '0.2178', '-0.4666', '0.1045', '0.9355', '-0.4714', '0.1571', '0.5415', '0.606', '-0.4036', '-0.5356', '0.1472', '0.2393', '-0.3997', '-0.0361', '0.303', '-0.2196', '-0.1879', '0.2297', '0.3152', '-0.05847', '0.2722', '-0.3494', '0.6523', '0.2883', '0.743', '0.06152', '0.03717', '-0.8496', '0.02843', '-0.991', '0.7056', '-0.684', '-0.1225', '0.2341', '0.3135', '-0.002062', '0.7188', '0.3325', '0.4802', '-0.6816', '0.11664', '0.1536', '0.63', '-0.5986', '0.3494', '-0.541', '0.576', '0.2095', '-0.573', '-0.6177', '-0.00976', '-0.329', '0.5107', '-0.5757', '-0.08124', '0.739', '0.6597', '0.7773', '0.56', '0.5576', '-0.1729', '0.792', '0.6313', '-0.34', '1.065', '-0.01402', '0.07385', '0.10046', '-0.3132', '0.5093', '-0.149', '-0.03354', '-0.7407', '0.3164', '0.0891', '0.1992', '0.2542', '-0.07043', '1.19', '0.4316', '0.2766', '0.5176', '0.1804', '0.4622', '-0.0913', '-0.667', '0.05682', '-0.1168', '0.1431', '-0.4165']",,,C536420,,,,
mondo:0009800,"Blount disease, adolescent","['Blount disease, adolescent', 'tibia vara, adolescent', 'Osteochondrosis deformans tibiae, adolescent']",,259200,,C3151572,,,,,,,,
mondo:0009801,"familial osteodysplasia, Anderson type","['osteodysplasia familial Anderson type', 'osteodysplasia, familial, Anderson type']",,259250,2769,C1850186,,,,C564923,,,,
mondo:0009802,"osteodysplasty, precocious, of Danks, Mayne, and Kozlowski","['osteodysplasty, precocious, of Danks, Mayne, and Kozlowski', 'osteodysplasty precocious of Danks Mayne and Kozlowski', 'Danks Mayne Kozlowski precocious osteodysplasty']",,259270,,C1850185,,,,C564922,,,,
mondo:0009803,congenital osteogenesis imperfecta-microcephaly-cataracts syndrome,"['osteogenesis imperfecta congenita, microcephaly, and cataracts']",,259410,2772,C1850184,,,,C537558,,Q78.0,,
mondo:0009804,osteogenesis imperfecta type 3,"['OI3', 'progressively deforming OI', 'OI type 3', 'progressive deforming osteogenesis imperfecta', 'OI type III', 'osteogenesis imperfecta, type 3', 'osteogenesis imperfecta, progressively deforming, with normal sclerae', 'osteogenesis imperfecta type III', 'progressively deforming osteogenesis imperfecta with normal sclera', 'OI, type 3', 'severe osteogenesis imperfecta', 'Oi3', 'osteogenesis imperfecta, type III', 'osteogenesis imperfecta, progressively deforming with normal sclerae']",0110339,259420,216812,C0268362,,C99002,,C536044,,,,
mondo:0009805,osteogenesis imperfecta type 9,"['osteogenesis imperfecta caused by mutation in PPIB', 'OI type IX', 'OI, type 9', 'PPIB osteogenesis imperfecta', 'OI 9', 'OI9', 'osteogenesis imperfecta, type 9', 'osteogenesis imperfecta, type IX', 'osteogenesis imperfecta type IX', 'osteogenesis imperfecta sillence type II/III without abnormality of type I collagen']",0110349,259440,216820,,"['-0.126', '-0.0051', '0.2893', '-0.1713', '0.3923', '-0.2925', '0.00813', '0.6504', '-0.1956', '0.05066', '-0.1152', '0.2194', '-0.1987', '-0.203', '-0.1752', '-0.1864', '0.5195', '-0.0808', '0.11676', '-0.3892', '0.2075', '0.026', '0.899', '0.0413', '-0.0151', '0.3171', '0.04175', '-0.2864', '-0.2688', '0.01923', '-0.1046', '-0.07196', '0.3132', '0.3997', '-0.03546', '-0.3977', '-0.71', '-0.5273', '-0.1833', '-0.5103', '-0.2534', '-0.3162', '0.10846', '0.0018215', '-0.541', '-0.3772', '0.1117', '0.5054', '0.3735', '-0.2314', '0.4617', '-0.5107', '0.337', '-0.1453', '0.01457', '-0.3306', '-0.2625', '-0.608', '-0.1287', '0.007175', '-0.06915', '0.1564', '0.006813', '-0.2006', '-0.415', '0.1544', '-0.00789', '0.5903', '-0.5425', '0.3447', '0.2478', '-0.0886', '0.03555', '-0.647', '0.2251', '0.1865', '-0.3962', '-0.09796', '0.2219', '-0.1525', '-0.08734', '0.011086', '-0.06082', '0.4878', '-0.6343', '0.4128', '0.0972', '0.2842', '0.76', '-0.03928', '0.04208', '0.4102', '0.02068', '0.3433', '0.676', '0.428', '0.2917', '-0.3662', '0.3618', '-0.2927']",,,C564921,,,,
mondo:0009806,Bruck syndrome 1,"['Bruck syndrome 1', 'arthrogryposis-like disorder', 'FKBP10 Bruck syndrome', 'Bruck syndrome type 1', 'Bruck syndrome caused by mutation in FKBP10', 'Kuskokwim disease', 'BRKS1']",,259450,,C1850168,,,,,,,,
mondo:0009807,osteosarcoma,"['osteosarcoma (disease)', 'osteosarcoma, malignant', 'osteogenic sarcoma', 'osteoid sarcoma', 'osteosarcoma', 'bone tissue neoplasm', 'sarcoma of osteoid']",3347,,,,"['0.383', '-0.598', '0.6177', '0.09576', '-0.2905', '-0.4365', '0.4302', '0.5347', '-0.7236', '-0.3093', '0.3257', '0.2484', '0.1437', '1.16', '-0.4521', '0.2864', '-0.634', '-0.4373', '-0.2366', '-0.6963', '0.2908', '-0.1948', '0.0248', '-0.1898', '-0.1174', '0.012184', '-0.3618', '0.11145', '-0.417', '-0.0713', '-0.2063', '-0.3928', '0.1107', '-0.2964', '0.4424', '0.05478', '-0.5312', '-0.1023', '-0.1539', '-0.2686', '-0.1787', '-0.3384', '-0.009285', '-0.3853', '0.3252', '0.271', '-0.3289', '-0.2937', '1.099', '-0.5615', '0.4304', '-0.1556', '0.467', '-0.03384', '-0.1497', '-0.4644', '-0.51', '0.4775', '-0.5107', '-0.3137', '0.42', '-0.12103', '-0.1793', '-0.0006013', '-0.5312', '0.707', '0.4192', '0.1818', '0.1356', '0.7773', '-0.0681', '0.0865', '0.1805', '-0.03775', '0.4578', '0.413', '-0.5713', '0.1126', '0.2178', '-1.051', '-0.4895', '0.128', '-0.3794', '0.7104', '-0.956', '-0.2695', '0.1484', '-0.698', '0.547', '-0.278', '0.1566', '-0.4617', '-0.247', '0.309', '0.533', '0.263', '0.2273', '-0.8906', '0.0769', '0.132']",C9145,0000637,D012516,,,,0002669
mondo:0009808,osteoid osteoma,"['osteoid osteoma (disease)', 'osteoid osteoma']",,259550,,C0029441,,C3297,,D010017,,,,0030433
mondo:0009809,"multicentric osteolysis, nodulosis, and arthropathy","['osteolysis, hereditary multicentric', 'Al-Aqeel Sewairi syndrome', 'Torg-Winchester syndrome', 'Torg syndrome', 'multicentric osteolysis, nodulosis, and arthropathy', 'Torg-Winchester syndrome, formerly', 'nodulosis-arthropathy-osteolysis syndrome', 'NAO syndrome', 'mona']",,259600,,,,C123437,,,,,,
mondo:0009810,autosomal recessive distal osteolysis syndrome,"['osteolysis, distal, with short stature, intellectual disability, and characteristic Facial appearance', 'distal osteolysis-short stature-intellectual disability syndrome', 'Petit-Fryns syndrome', 'osteolysis, distal, with short stature, mental retardation, and characteristic facial appearance', 'osteolysis, distal, with short stature, intellectual disability, and characteristic facial appearance', 'osteolysis syndrome recessive', 'osteolysis, distal, with short stature, mental retardation, and characteristic Facial appearance', 'osteolysis syndrome, recessive']",,259610,2776,C4275111,,,,C536052,,,,
mondo:0009811,osteoma of middle ear,['osteoma of middle ear'],,259650,,C1850142,,,,C564917,,,,
mondo:0009813,chronic recurrent multifocal osteomyelitis,"['CRMO', 'NBO', 'CMO', 'chronic multifocal osteomyelitis', 'non-bacterial osteomyelitis', 'CNO/CRMO', 'multifocal osteomyelitis, chronic', 'chronic recurrent multifocal osteomyelitis (disease)', 'osteomyelitis, chronic multifocal', 'chronic nonbacterial osteomyelitis/chronic recurrent multifocal osteomyelitis', 'chronic recurrent multifocal osteomyelitis']",0060645,259680,324964,C0410422,,C119042,,C535456,,,,0002754
mondo:0009814,osteopenia-intellectual disability-sparse hair syndrome,"['osteopenia and sparse hair', 'Kaler Garrity Stern syndrome', 'Kaler-Garrity-Stern syndrome', 'osteopenia mental retardation sparse hair', 'osteopenia intellectual disability sparse hair']",,259690,2324,C1850140,,,,C537706,,,,
mondo:0009815,autosomal recessive osteopetrosis 1,"['TCIRG1 autosomal recessive osteopetrosis', 'osteopetrosis, autosomal recessive type 1', 'Albers-Schonberg disease, autosomal recessive', 'TCIRG1 autosomal recessive malignant osteopetrosis', 'autosomal recessive Albers-Schonberg disease', 'osteopetrosis, infantile malignant 1', 'autosomal recessive osteopetrosis type 1', 'infantile malignant osteopetrosis 1', 'autosomal recessive malignant osteopetrosis caused by mutation in TCIRG1', 'OPTB1', 'marble bones, autosomal recessive', 'osteopetrosis, autosomal recessive 1', 'marble bones autosomal recessive', 'osteopetrosis infantile malignant 1', 'osteopetrosis autosomal recessive 1']",0110942,259700,,,,C167215,,C564915,,,,
mondo:0009816,autosomal recessive osteopetrosis 2,"['mild autosomal recessive form osteopetrosis', 'osteopetrosis autosomal recessive 2', 'osteopetrosis, autosomal recessive type 2', 'OPTB2', 'autosomal recessive malignant osteopetrosis caused by mutation in TNFSF11', 'TNFSF11 autosomal recessive malignant osteopetrosis', 'osteoclast-poor osteopetrosis', 'osteopetrosis, autosomal recessive 2', 'autosomal recessive osteopetrosis type 2', 'osteopetrosis osteoclast-poor', 'osteopetrosis, mild autosomal recessive form', 'osteopetrosis, osteoclast-poor', 'TNFSF11 autosomal recessive osteopetrosis']",0110943,259710,,,,,,C536059,,,,
mondo:0009817,autosomal recessive osteopetrosis 5,"['infantile malignant osteopetrosis 3', 'osteopetrosis, autosomal recessive type 5', 'OPTB5', 'osteopetrosis, autosomal recessive 5', 'osteopetrosis, infantile malignant 3', 'osteopetrosis autosomal recessive 5', 'OSTM1 osteopetrosis (disease)', 'osteopetrosis infantile malignant 3', 'autosomal recessive osteopetrosis type 5']",0110939,259720,,,,,,C566883,,,,
mondo:0009818,autosomal recessive osteopetrosis 3,"['osteopetrosis, autosomal recessive 3', 'autosomal recessive osteopetrosis type 3', 'carbonic anhydrase II deficiency', 'mixed RTA', 'mixed renal tubular acidosis', 'osteopetrosis with renal tubular acidosis', 'osteopetrosis, autosomal recessive 3, with renal tubular acidosis', 'Guibaud Vainsel syndrome', 'Autosomal Recessive osteopetrosis, type 3', 'osteopetrosis autosomal recessive 3', 'OPTB3', 'marble brain disease', 'carbonic anhydrase 2 deficiency', 'renal tubular acidosis type 3', 'osteopetrosis, autosomal recessive type 3', 'autosomal recessive osteopetrosis 3 with renal tubular acidosis', 'CA2 osteopetrosis (disease)', 'Guibaud-Vainsel syndrome']",0110941,259730,2785,,"['0.0966', '-0.1073', '0.3801', '-0.3462', '0.2588', '-0.1451', '-0.267', '1.415', '0.1112', '-0.5845', '-0.01768', '-1.025', '-0.4937', '-0.1644', '0.5845', '0.125', '0.1118', '-0.611', '-0.2186', '-1.064', '0.5303', '-0.1547', '0.947', '-0.2834', '0.4204', '0.1686', '-0.3342', '-0.382', '-0.269', '-0.5684', '-0.04623', '-0.02284', '0.3638', '-0.1334', '-0.10516', '-0.266', '-0.1858', '-0.8257', '-0.1775', '-0.2103', '-0.003422', '-0.3071', '0.2725', '0.001534', '0.01433', '-0.9175', '0.1526', '-0.264', '0.2627', '-0.3442', '-0.005764', '0.2761', '0.409', '-0.0002182', '-0.2042', '-0.3335', '0.511', '0.282', '-0.4175', '0.3916', '0.58', '-0.531', '-0.3655', '-0.62', '-0.153', '-0.4133', '-0.0002985', '0.9976', '-0.667', '0.2095', '-0.27', '-0.3833', '-0.05215', '0.334', '0.02687', '0.1416', '0.07764', '0.4192', '-0.2834', '0.06744', '0.1292', '-0.5493', '0.0925', '0.729', '-0.6104', '0.3108', '0.206', '-0.1803', '0.137', '-0.0427', '-0.05893', '-0.2451', '-0.5283', '0.1764', '-0.07166', '0.3088', '0.3467', '-0.0362', '0.09924', '0.4597']",C118438,,C536058,588.89,,,
mondo:0009820,osteoporosis-pseudoglioma syndrome,"['pseudoglioma with bone fragility', 'OPPG', 'osteogenesis imperfecta ocular form', 'Ops', 'osteogenesis imperfecta, ocular form', 'osteoporosis-pseudoglioma syndrome', 'ocular form of osteogenesis imperfecta', 'osteoporosis pseudoglioma syndrome']",0060849,259770,2788,C0432252,"['0.3198', '-0.2456', '0.0555', '0.6514', '0.2722', '-0.57', '-0.78', '0.6675', '-0.68', '-0.8247', '0.298', '0.5884', '-0.06946', '0.361', '-0.3093', '-0.1597', '0.001818', '0.715', '-0.77', '-0.0674', '-0.236', '-0.3364', '0.0462', '-0.3342', '0.3213', '-0.165', '0.09186', '-0.7524', '-0.6025', '-0.1559', '0.49', '-0.632', '-0.1154', '-0.4114', '-0.08044', '-0.1549', '0.04944', '-0.7563', '0.08417', '-0.818', '0.12256', '-0.1576', '0.2786', '-0.2861', '0.5063', '-0.5483', '0.2844', '0.3135', '0.4424', '0.4841', '0.752', '0.287', '0.4324', '-0.2827', '-0.5283', '-0.513', '-0.3215', '0.1621', '-0.525', '-0.1554', '0.2942', '0.1263', '-0.6978', '-0.5425', '-0.01282', '0.6963', '0.444', '0.721', '-0.1964', '-0.4287', '0.499', '-0.266', '0.0427', '-0.4438', '0.2937', '0.541', '-0.2866', '0.586', '-0.1121', '0.4832', '0.165', '-0.4912', '0.2286', '0.67', '-0.4797', '0.753', '0.3289', '0.01497', '1.347', '0.2076', '-0.3086', '-0.1958', '-0.8545', '-0.1343', '0.4595', '-0.415', '0.09436', '-0.5386', '-0.2673', '-0.547']",C130998,,C536063,,,10052452,
mondo:0009821,lethal osteosclerotic bone dysplasia,"['Raine syndrome', 'combination of microcephaly, exophthalmos, hypoplastic nose and midface, gum hyperplasia, cleft palate, apparently low-set ears, and osteosclerosis', 'osteosclerotic bone dysplasia, lethal', 'osteomalacia, sclerosing, with cerebral calcification', 'RNS', 'RAINE syndrome']",,259775,1832,C1850141,"['-0.1873', '-0.04694', '0.461', '-0.61', '-0.04645', '0.0808', '-0.1176', '1.1875', '-0.4568', '-0.1421', '-0.547', '-0.961', '-0.5034', '-0.7812', '0.2969', '0.03387', '-0.147', '-0.6133', '-0.4717', '-0.5195', '0.6304', '-0.2185', '0.918', '-0.359', '0.806', '0.229', '-0.2917', '-0.0927', '0.1131', '-0.4067', '0.03598', '-0.302', '-0.04834', '-0.1155', '0.4976', '0.3535', '-0.4128', '-0.1744', '0.2283', '-0.8145', '-0.0961', '-0.03174', '-0.09937', '0.1575', '-0.01096', '-0.7104', '0.3174', '-0.01843', '0.2443', '-0.3345', '0.1278', '-0.0938', '0.3215', '0.4292', '-0.163', '-0.3774', '0.3938', '0.3665', '0.0936', '0.2515', '0.235', '-0.1489', '-0.3542', '-0.465', '-0.1886', '-0.36', '0.5845', '0.5586', '-0.1841', '0.6035', '-0.2878', '0.2183', '0.1514', '0.5024', '-0.674', '0.1635', '0.5625', '0.3838', '0.0052', '-0.1449', '-0.3967', '-0.0319', '0.0546', '0.618', '-0.359', '0.07904', '0.0884', '-0.014114', '-0.1107', '0.00774', '0.003477', '-0.07513', '0.02577', '0.418', '0.8276', '0.3877', '0.9185', '-0.3079', '0.4673', '0.06384']",,,C564916,,,,
mondo:0009822,otoonychoperoneal syndrome,"['otoonychoperoneal syndrome', 'oto-onycho-peroneal syndrome']",,259780,2793,C1850105,,,,C564912,759.89,,,
mondo:0009823,primary hyperoxaluria type 1,"['glycolic aciduria', 'serine:pyruvate aminotransferase deficiency', 'primary hyperoxaluria caused by mutation in AGXT', 'primary hyperoxaluria type I', 'Oxalosis 1', 'serine pyruvate aminotransferase deficiency', 'HP1', 'hyperoxaluria, primary, type 1', 'peroxisomal alanine glyoxylate aminotransferase deficiency', 'peroxisomal alanine:glyoxylate aminotransferase deficiency', 'AGXT primary hyperoxaluria', 'PH1', 'peroxisomal alanine-glyoxylate aminotransferase deficiency', 'hyperoxaluria, primary, type I', 'alanine-glyoxylate aminotransferase deficiency', 'hepatic AGT deficiency']",0111670,259900,93598,C0268164,"['-0.1469', '0.2922', '0.0462', '0.06396', '0.1195', '-0.2397', '-0.10657', '0.00636', '-0.3154', '0.346', '-0.1268', '0.02518', '-0.0685', '-0.0336', '-0.24', '-0.2576', '0.0918', '-0.04086', '-0.04343', '-0.5596', '-0.1149', '-0.297', '0.6157', '-0.1931', '-0.0419', '0.1813', '0.01724', '-0.2306', '-0.0694', '-0.185', '0.2274', '0.2717', '0.3987', '0.1803', '-0.1571', '-0.6934', '-0.04404', '-0.1345', '-0.2434', '-0.1575', '-0.05078', '-0.404', '0.4458', '-0.12103', '-0.2834', '-0.1973', '-0.01869', '-0.01241', '0.04208', '0.1752', '0.1711', '-0.0614', '0.1503', '-0.2605', '-0.3518', '-0.338', '0.3533', '-0.3047', '-0.4304', '-0.0459', '0.4026', '0.0827', '0.1832', '-0.2554', '0.3254', '-0.1042', '0.4062', '0.1731', '-0.3691', '-0.2673', '-0.333', '-0.1247', '0.10065', '-0.06384', '0.414', '-0.02884', '0.05746', '-0.0353', '-0.1699', '-0.10187', '0.04813', '0.1407', '-0.0642', '0.142', '0.1062', '0.169', '0.269', '-0.024', '0.4634', '-0.1863', '0.3215', '0.2808', '-0.2074', '-0.2913', '0.5615', '0.2244', '0.478', '-0.2428', '0.03284', '0.2024']",C123212,,C536414,271.8,,,
mondo:0009824,primary hyperoxaluria type 2,"['L-glyceric aciduria', 'hyperoxaluria, primary, type 2', 'HP2', 'primary hyperoxaluria caused by mutation in GRHPR', 'Oxalosis 2', 'glyoxylate reductase/hydroxypyruvate reductase deficiency', 'glyceric aciduria', 'hyperoxaluria, primary, type II', 'GRHPR primary hyperoxaluria', 'D-glycerate dehydrogenase deficiency', 'primary hyperoxaluria type II']",0111671,260000,93599,C0268165,"['-0.2202', '0.1501', '-0.05566', '-0.03102', '0.079', '-0.2527', '-0.2285', '0.0535', '-0.325', '0.1838', '-0.2261', '0.0549', '-0.0177', '-0.00633', '-0.168', '-0.258', '0.197', '0.06805', '0.0528', '-0.5405', '-0.08746', '-0.3713', '0.555', '-0.14', '-0.0245', '0.0976', '0.05237', '-0.1426', '-0.1065', '-0.233', '0.208', '0.4133', '0.4175', '0.3723', '-0.1295', '-0.579', '0.05862', '-0.2268', '-0.2125', '-0.183', '-0.02596', '-0.4297', '0.4744', '-0.0352', '-0.2876', '-0.2114', '0.1095', '0.0562', '0.01236', '0.3423', '0.11346', '-0.05566', '0.2118', '-0.3113', '-0.2238', '-0.2922', '0.3438', '-0.3008', '-0.513', '0.0881', '0.435', '0.1366', '0.3032', '-0.3284', '0.3628', '-0.1581', '0.3694', '0.1858', '-0.3591', '-0.1661', '-0.344', '-0.2798', '0.11475', '-0.05563', '0.4631', '0.09705', '0.05496', '0.1519', '-0.2352', '0.0004687', '-0.014465', '0.1923', '-0.0636', '0.117', '0.1663', '0.1326', '0.4004', '0.0096', '0.535', '-0.0647', '0.286', '0.3872', '-0.10895', '-0.364', '0.4922', '0.2927', '0.5996', '-0.335', '0.03278', '0.2228']",C123213,,C536415,271.8,,,
mondo:0009825,5-oxoprolinase deficiency,"['5-oxoprolinase deficiency', 'oxoprolinuria due to oxoprolinase deficiency', 'OPLAHD', 'oxoprolinuria due to 5-oxoprolinase deficiency', '5-oxoprolinase deficiency (disease)', 'rare inborn error of 5-oxoprolinase (ATP-hydrolyzing) activity', '5-alpha-oxoprolinase deficiency', 'inborn error of 5-oxoprolinase (ATP-hydrolyzing) activity']",,260005,33572,C0268525,"['-0.541', '0.5146', '-0.293', '0.0901', '0.1926', '-0.641', '-0.5566', '0.4353', '0.05673', '-0.1962', '-0.1387', '0.1962', '0.06335', '-0.1442', '0.1571', '0.02655', '-0.02841', '-0.0596', '0.08374', '-0.7993', '0.2903', '-0.2515', '0.3262', '0.1099', '0.0691', '-0.01249', '0.136', '-0.05142', '-0.3855', '-0.5513', '0.6113', '-0.04965', '0.1384', '0.225', '-0.3147', '-0.175', '-0.1247', '-0.1566', '-0.3247', '0.1268', '0.02666', '-0.1902', '0.4365', '-0.1667', '-0.2805', '-0.5903', '0.03885', '-0.233', '-0.11884', '-0.1506', '-0.1979', '-0.6177', '0.0747', '0.2408', '0.1642', '-0.0981', '0.2383', '-0.2795', '-0.0945', '0.738', '0.0783', '0.03995', '0.2844', '-0.07153', '0.02942', '0.002117', '0.04892', '0.11633', '-0.6914', '0.2773', '-0.02832', '-0.5513', '-0.087', '-0.1034', '0.735', '0.1084', '0.10236', '-0.1604', '0.18', '0.1794', '0.4834', '0.0632', '0.01388', '0.0766', '0.0694', '0.1173', '0.129', '-0.01596', '0.2993', '0.007565', '0.7354', '-0.05704', '-0.3613', '-0.4292', '1.006', '0.657', '-0.0414', '-0.3', '-0.01581', '0.1158']",,,C535322,270.8,,,0040142
mondo:0009826,PA polymorphism of alpha-2-globulin,"['Alpha-2-globulin polymorphism Pa', 'PA polymorphism of alpha-2-globulin']",,260100,,,,,,,,,,
mondo:0009828,palant cleft palate syndrome,"['Palant cleft palate syndrome', 'unusual facies, cleft palate, intellectual disability, and limb abnormalities', 'unusual facies, cleft palate, mental retardation, and limb abnormalities']",,260150,,C1850102,,,,C538102,,,,
mondo:0009830,parkinsonian-pyramidal syndrome,"['autosomal recessive early-onset Parkinson disease 15', 'PARK15', 'autosomal recessive early-onset Parkinson^s disease 15', 'autosomal recessive early-onset Parkinson disease type 15', 'pallidopyramidal syndrome', 'parkinsonian-pyramidal syndrome', 'pallido-pyramidal syndrome', 'Parkinson disease 15, autosomal recessive', 'pallido-pyramidal disease', 'Pallidopyramidal syndrome', 'Parkinson disease 15, autosomal recessive early-onset']",0060372,260300,171695,C1850100,"['-0.2815', '0.2472', '-0.09906', '-0.1584', '0.1737', '-0.4', '-0.2245', '0.1682', '-0.5312', '0.423', '-0.01534', '0.03305', '0.2306', '-0.08704', '0.418', '-0.1134', '0.007145', '-0.3518', '-0.2778', '-0.68', '-0.07697', '0.1859', '0.3303', '0.0894', '-0.02693', '0.146', '0.05014', '0.2252', '-0.2964', '0.0736', '0.2458', '0.3938', '0.519', '-0.0726', '0.2712', '-0.1153', '-0.3677', '-0.1298', '-0.01376', '-0.2832', '0.2717', '-0.3582', '-0.10944', '-0.1573', '0.1577', '-0.481', '-0.01025', '0.1995', '0.10944', '-0.0372', '-0.3262', '0.4336', '-0.3494', '-0.4255', '0.254', '-0.1838', '0.313', '-0.0504', '-0.4846', '-0.1221', '0.0434', '0.03793', '0.2625', '-0.03674', '-0.2856', '0.4607', '0.2605', '0.1561', '-0.3015', '0.2454', '-0.4702', '-0.1675', '0.09705', '-0.0803', '0.1334', '0.2229', '0.02554', '0.1107', '0.101', '-0.573', '0.397', '-0.3213', '0.392', '0.3032', '0.03012', '0.0258', '0.1384', '0.4175', '0.3733', '0.12384', '0.24', '-0.1644', '-0.03833', '-0.04138', '0.2233', '0.4802', '0.416', '0.3174', '0.06216', '0.3438']",,,C538104,,,,
mondo:0009831,malignant pancreatic neoplasm,"['malignant neoplasm of body of pancreas', 'pancreas cancer', 'Ca body of pancreas', 'Ca head of pancreas', 'Ca tail of pancreas', 'malignant neoplasm of tail of pancreas', 'malignant pancreatic neoplasm', 'malignant neoplasm of the pancreas', 'pancreatic cancer', 'pancreatic tumour', 'malignant pancreas neoplasm', 'pancreas neoplasm', 'cancer of pancreas', 'malignant neoplasm of pancreas', 'malignant neoplasm of head of pancreas']",1793,,,,"['-0.1315', '0.1461', '0.0501', '0.00231', '0.1359', '-0.09894', '0.1201', '0.12354', '-0.01921', '-0.0528', '-0.07263', '0.05368', '0.0268', '0.01134', '-0.1917', '-0.1051', '-0.03223', '-0.0775', '-0.06143', '-0.3127', '0.031', '-0.12213', '0.1605', '-0.1329', '-0.010574', '-0.1204', '0.04077', '0.02022', '-0.02545', '-0.1522', '0.1667', '-0.0174', '0.1395', '-0.08203', '0.0758', '-0.03384', '-0.12085', '-0.02896', '-0.07184', '-0.0837', '0.0351', '-0.1089', '0.10645', '-0.05527', '-0.004257', '-0.0685', '-0.0241', '0.04358', '0.1245', '0.0834', '-0.0285', '-0.0351', '0.1119', '0.1737', '-0.09576', '-0.00768', '0.0931', '-0.0553', '-0.267', '-0.05917', '0.2411', '0.05557', '-0.05807', '0.01646', '-0.002274', '0.04977', '0.2233', '0.1869', '-0.08044', '0.1393', '-0.0258', '-0.03854', '0.0938', '-0.01245', '0.0516', '0.02383', '-0.00925', '0.02983', '-0.0424', '-0.2115', '-0.2411', '0.0442', '-0.1114', '0.0328', '-0.19', '-0.09033', '0.1383', '0.07166', '0.1771', '-0.1333', '0.154', '0.06696', '-0.00896', '-0.1089', '0.4263', '-0.0419', '0.11414', '-0.2852', '-0.08325', '0.1677']",C9005,1000359,,157.8,,,
mondo:0009832,pancreatic agenesis,"['congenital pancreatic agenesis', 'partial agenesis of the pancreas', 'pancreatic agenesis 1', 'PAGEN1', 'partial pancreatic agenesis', 'pancreatic agenesis type 1']",0050877,,2805,C1850096,"['-0.4807', '-0.00427', '-0.3074', '0.244', '0.637', '-0.2788', '-0.1392', '0.304', '-0.3071', '-0.2032', '-0.809', '-0.1709', '0.0889', '-0.02417', '-0.567', '-0.4128', '0.178', '-0.1062', '-0.627', '-0.8887', '0.258', '-0.3564', '0.545', '-0.8096', '-0.0213', '0.499', '-0.403', '0.603', '0.7876', '-0.3337', '0.247', '-0.64', '0.6206', '0.2322', '0.3447', '-0.161', '-0.1272', '0.06287', '-0.2705', '0.716', '-0.06354', '0.02126', '0.1914', '-0.0968', '0.1603', '0.10095', '0.0411', '-0.256', '-0.0736', '-0.1735', '0.1909', '0.1487', '-0.0719', '0.6562', '-0.5605', '0.0742', '0.2175', '0.008156', '-0.565', '-0.005295', '0.254', '0.617', '0.4307', '-0.6304', '-0.412', '0.4358', '0.0913', '0.3716', '-0.3904', '-0.263', '-0.013626', '0.2822', '0.153', '0.527', '0.817', '-0.1993', '0.7554', '0.3643', '0.1656', '-0.3557', '-0.4204', '0.0368', '0.5312', '0.0136', '-0.2465', '0.274', '0.7236', '0.9463', '0.2578', '-0.276', '0.391', '0.2837', '0.03085', '-0.502', '1.36', '-0.6987', '0.1722', '-1.111', '-0.474', '0.2311']",,,C564908,,,,
mondo:0009833,Shwachman-Diamond syndrome,"['Schwachman-Diamond syndrome', 'pancreatic insufficiency and bone marrow dysfunction', 'Shwachman-Diamond type metaphyseal dysplasia', 'congenital lipomatosis of pancreas', 'Shwachman-Diamond syndrome', 'SDS', 'Shwachman-Bodian-Diamond syndrome', 'Shwachman syndrome', 'Schwachmann-Diamond syndrome', 'lipomatosis of pancreas, congenital', 'Shwachman-Bodian syndrome']",0080023,,811,,"['-0.3738', '0.1469', '0.1106', '-0.8545', '0.2812', '-0.2026', '0.6963', '0.8325', '-0.1769', '-0.433', '0.03748', '-0.0793', '0.3271', '0.252', '-0.039', '-0.01921', '-0.2487', '-0.34', '-0.08276', '-0.935', '-0.1829', '-0.3037', '0.74', '-0.243', '0.2678', '-0.001194', '-0.1123', '-0.03047', '0.6143', '-0.5127', '0.2708', '-0.04764', '0.0788', '0.3909', '0.2686', '-0.2167', '-0.597', '-0.895', '-0.3018', '-0.05325', '-0.5283', '0.341', '0.2075', '-0.1842', '-0.221', '0.03', '-0.02858', '-0.2373', '0.597', '0.2854', '-0.02118', '0.0659', '0.3455', '0.0695', '0.484', '-0.7256', '0.1573', '-0.529', '-0.3455', '0.3398', '0.321', '0.1515', '-0.409', '-0.4783', '0.608', '0.1492', '0.1364', '0.11615', '-0.4243', '0.2705', '-0.1854', '-0.4446', '-0.6196', '-0.1794', '0.4668', '-0.802', '0.5137', '-0.7134', '0.2216', '0.1411', '-0.4197', '0.2607', '-0.6504', '0.2008', '-0.687', '0.1365', '0.503', '0.6533', '0.5996', '0.2163', '-0.05682', '-0.0909', '-0.3735', '-0.04108', '0.08606', '0.326', '0.6', '-0.3958', '0.6265', '-0.1137']",C61235,,C537330,,,10067940,
mondo:0009835,subacute sclerosing panencephalitis,"['SSPE', 'Subacute sclerosing leukoencephalitis', 'Van Bogaert encephalitis', 'Dawson^s encephalitis', 'Dawson encephalitis', 'Dawson disease', 'Subacute sclerosing panencephalitis', 'Subacute sclerosing panencephalitis (disorder) [ambiguous]', 'Subacute inclusion body encephalitis', 'Immunosuppressive measles encephalitis', 'Van Bogaert^s sclerosing leukoencephalitis', 'subacute sclerosing leukoencephalopathy', 'subacute sclerosing panencephalitis', 'panencephalitis, SUBACUTE sclerosing', 'Van Bogaert disease']",8970,260470,2806,C0038522,,C85171,0007502,D013344,046.2,A81.1,,
mondo:0009836,"pancreatitis, sclerosing cholangitis, and sicca complex","['pancreatitis, sclerosing cholangitis, and sicca complex']",,260480,,C1850080,,,,C564906,,,,
mondo:0009837,choroid plexus papilloma,"['childhood papilloma of choroid plexus', 'CPP', 'childhood choroid plexus papilloma', 'papilloma of choroid plexus', 'papilloma, choroid plexus, benign', 'choroid plexus papilloma', 'papilloma of the choroid plexus', 'choroid plexus papilloma NOS (morphologic abnormality)', 'paediatric papilloma of choroid plexus', 'choroid plexus papilloma, no ICD-O subtype', 'choroid plexus carcinoma', 'pediatric papilloma of choroid plexus']",2626,260500,2807,C0205770,"['-0.153', '0.2245', '0.2253', '-0.2861', '-0.03543', '-0.0324', '0.679', '0.4695', '-0.3267', '0.0554', '-0.04312', '-0.3674', '-0.1227', '0.0775', '-0.1033', '-0.5796', '0.1307', '-0.509', '0.3528', '-0.2354', '-0.1059', '-0.374', '0.1307', '-0.4727', '0.1201', '0.1516', '0.05792', '0.2166', '-0.3071', '0.4116', '0.02026', '-0.245', '0.4724', '-0.2786', '-0.2124', '0.4526', '0.01147', '0.2993', '0.0874', '-0.3474', '0.3506', '-0.4805', '0.3618', '-0.153', '0.271', '0.3223', '0.2308', '0.2339', '0.2218', '0.3997', '0.279', '0.4705', '-0.5996', '-0.5845', '-0.07574', '-0.01692', '0.2411', '-0.10913', '-0.4448', '0.3054', '-0.09467', '0.2737', '-0.1095', '-0.152', '-0.4421', '-0.0797', '0.4', '0.1187', '-0.1831', '0.4092', '0.1545', '0.579', '0.2737', '-0.369', '-0.05292', '0.449', '-0.2258', '-0.1203', '-0.4832', '-0.559', '-0.5854', '0.1976', '0.22', '-0.04868', '-0.1561', '-0.4172', '0.3608', '0.2246', '0.3066', '-0.3662', '0.1796', '0.2883', '0.2333', '-0.2798', '0.911', '0.351', '0.3894', '0.1166', '0.2015', '-0.04214']",C3698,1000177,D020288,,,10008777,
mondo:0009838,Parana hard-skin syndrome,"['hard skin syndrome Parana type', 'hard-skin syndrome, Parana type', 'Parana hard-skin syndrome', 'hard skin syndrome, Parana type', 'Parana hard skin syndrome']",,260530,2812,C1850079,,C126559,,C564905,,,,
mondo:0009839,progressive supranuclear palsy-parkinsonism syndrome,"['PSP-p', 'progressive supranuclear palsy atypical', 'atypical PSP', 'Steele-Richardson-Olszewski syndrome, atypical', 'supranuclear palsy, progressive atypical', 'Parkinson-dementia syndrome', 'supranuclear palsy, progressive, 1, atypical', 'PSP-parkinsonism']",,260540,240085,CN201680,"['0.3533', '1.35', '0.07697', '0.01749', '-0.4548', '-0.664', '0.29', '0.47', '-1.019', '0.3528', '0.79', '-0.1153', '-0.5093', '0.5254', '0.3237', '-0.3', '-0.2668', '-0.7715', '-0.752', '-0.3086', '0.088', '0.10034', '0.04874', '0.06058', '0.2922', '0.1877', '0.27', '-0.0628', '-0.2769', '1.231', '0.1844', '-0.0254', '0.2522', '0.012566', '0.1009', '0.07074', '0.4204', '-0.1327', '0.03726', '-0.642', '1.027', '-0.2856', '-0.4243', '0.3765', '0.4307', '-0.1729', '0.126', '-0.464', '0.08624', '0.6567', '0.1132', '0.3137', '-0.31', '-1.056', '0.2179', '-0.631', '0.002525', '-0.4382', '-0.04053', '-0.08514', '0.2983', '-0.2542', '-0.718', '-0.1813', '-0.2107', '0.5474', '0.2815', '-0.0682', '-0.5156', '0.793', '-0.297', '-0.10864', '0.1488', '-0.6094', '0.5586', '0.4458', '-0.1346', '0.2352', '-0.0618', '0.278', '0.2157', '-1.309', '0.1005', '0.5713', '0.1467', '-0.1688', '0.2698', '-0.06384', '0.746', '-0.5454', '0.539', '0.3174', '-0.5156', '0.9766', '0.1974', '0.9375', '0.0659', '-0.1759', '0.4146', '0.1678']",,,C537240,,,,
mondo:0009840,Partington-Anderson syndrome,['Partington-Anderson syndrome'],,260555,2829,CN202825,,,,C536299,,,,
mondo:0009841,PEHO syndrome,"['peho', 'infantile Cerebellooptic atrophy', 'progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy', 'peho-like syndrome', 'peho syndrome', 'progressive encephalopathy-optic atrophy syndrome', 'progressive encephalopathy with edema, hypsarrhythmia and optic atrophy']",0080539,260565,2836,C1850055,"['-0.1766', '0.0823', '-0.01543', '0.0245', '-0.1753', '-0.709', '0.1906', '0.7285', '-0.6562', '-0.4158', '-0.507', '-0.2783', '-0.0554', '-0.5317', '-0.3965', '-0.02171', '0.563', '-0.1971', '-0.2347', '-0.268', '0.1237', '-0.2517', '0.2617', '-0.1967', '0.0725', '-0.3523', '-0.5444', '0.114', '-0.543', '-0.3816', '0.4404', '0.2974', '0.04166', '0.011055', '-0.1847', '0.5015', '0.273', '-0.131', '-0.3127', '0.0925', '0.00821', '-0.2378', '-0.1855', '-0.3376', '0.1063', '0.08795', '0.0365', '0.4854', '-0.3428', '0.5557', '-0.729', '0.3755', '-0.2169', '-0.2471', '-0.06192', '-0.6587', '0.4788', '-0.02342', '0.0847', '0.543', '-0.3496', '-0.06396', '-0.005535', '0.1268', '-0.09033', '0.11035', '1.075', '0.09503', '-0.1086', '0.328', '-0.4426', '0.2129', '0.5215', '0.0438', '-0.1382', '0.5366', '0.1945', '-0.06573', '-0.578', '0.4985', '0.1313', '0.076', '-0.1346', '0.4712', '-0.09143', '-0.321', '0.1652', '0.3574', '0.355', '0.684', '-0.002474', '0.11646', '0.1981', '-0.4412', '0.11115', '0.1849', '0.509', '-0.2593', '0.546', '0.011375']",,,C536317,,,,
mondo:0009842,Pelger-Huet-like anomaly and episodic fever with abdominal pain,"['Pelger-Huet-like anomaly and episodic fever with abdominal pain', 'immunodeficiency 108 with autoinflammation']",,260570,,C1850054,,,,C564899,,,,
mondo:0009843,hypomyelinating leukodystrophy 3,"['HLD3', 'hypomyelinating leukodystrophy type 3', 'leukodystrophy, hypomyelinating, 3', 'perinatal Sudanophilic leukodystrophy', 'leukodystrophy, hypomyelinating, type 3', 'AIMP1 leukodystrophy', 'leukodystrophy caused by mutation in AIMP1', 'leukodystrophy, hypomyelinating 3', 'Pelizaeus-Merzbacher-like disease due to AIMP1 mutation']",0060790,260600,280293,C1850053,"['-0.2047', '0.2269', '-0.004543', '0.02373', '0.0759', '-0.2793', '-0.05084', '0.1654', '-0.3147', '-0.1025', '-0.02104', '-0.009155', '-0.09784', '-0.014366', '0.1477', '-0.2012', '-0.0906', '-0.0916', '-0.1276', '-0.262', '0.1049', '-0.1315', '0.0903', '0.02173', '0.1016', '-0.02939', '-0.01765', '0.0675', '0.022', '-0.02551', '0.12006', '0.04633', '0.219', '0.03119', '0.11475', '-0.1261', '-0.01752', '-0.0607', '0.09686', '-0.2225', '0.1123', '-0.197', '0.1042', '0.01822', '-0.1144', '-0.1932', '0.01543', '0.03836', '0.1682', '0.02867', '0.05585', '-0.05652', '0.004738', '0.00615', '-0.1128', '-0.1349', '0.3262', '0.04373', '-0.235', '0.0657', '0.07477', '0.1516', '0.1794', '-0.0265', '0.1007', '0.1892', '0.1671', '0.06885', '-0.1798', '0.1265', '-0.2173', '0.003588', '0.0798', '-0.1666', '0.1208', '0.0497', '0.0669', '0.1102', '-0.11725', '0.002476', '-0.07495', '-0.0836', '-0.05627', '0.09863', '-0.02808', '-0.1396', '0.1837', '0.2507', '0.2487', '0.1454', '0.07153', '0.02397', '-0.04092', '-0.0811', '0.4302', '0.174', '0.1904', '-0.3064', '-0.02895', '-0.00945']",,,C536319,,,,
mondo:0009844,pellagra-like syndrome,"['pellagra-like rash with neurologic manifestations', 'pellagra-like syndrome', 'pellagra-like skin rash-neurological manifestations syndrome', 'pellagra like syndrome']",,260650,2837,C1850052,,,,C538352,,,,
mondo:0009845,pelviscapular dysplasia,"['familial pelvis-scapular dysplasia', 'COUSIN syndrome', 'craniofacial Dysmorphism, hypoplasia of scapula and pelvis, and short stature', 'pelviscapular dysplasia', 'Cousin syndrome', 'craniofacial dysmorphism, hypoplasia of scapula and pelvis and short stature']",,260660,93333,C1850040,"['-0.0775', '0.338', '0.1215', '-0.2925', '0.2927', '-0.1981', '-0.1774', '0.4229', '-0.224', '-0.2974', '0.3186', '-0.1103', '0.2737', '0.03088', '0.3098', '0.811', '0.4526', '-0.2544', '-0.05588', '-0.4424', '-0.507', '0.248', '0.964', '0.2544', '-0.10095', '-0.0906', '-0.331', '0.1268', '0.588', '-0.4624', '0.7983', '-0.5317', '0.1332', '0.00659', '0.251', '-0.292', '-0.3054', '-0.634', '-0.4387', '-0.8433', '-0.0965', '-0.318', '0.1337', '-0.503', '-0.4343', '-0.3252', '0.3447', '0.465', '0.02432', '-0.6963', '0.4224', '-0.1877', '0.01837', '0.352', '-0.05524', '-0.8716', '0.1112', '-0.1687', '0.182', '0.2734', '0.1498', '-0.2179', '-0.6733', '0.3145', '-0.0284', '0.1602', '0.3071', '0.4192', '-0.538', '0.428', '-0.5635', '0.5146', '0.4932', '-0.3809', '-0.09973', '0.2615', '-0.2333', '-0.3096', '-0.3076', '0.1565', '0.12085', '0.5024', '0.06366', '0.6743', '-0.646', '-0.138', '-0.0641', '0.3918', '0.3105', '0.03452', '-0.3706', '0.4739', '0.2666', '0.0975', '0.6606', '0.1733', '0.1742', '-0.36', '0.1384', '-0.1528']",,,C535550,,,,
mondo:0009846,pentosuria,"['L-Xylulosuria', 'xylitol dehydrogenase deficiency', 'PNTSU', 'L-xylulose reductase deficiency', 'pentosuria', 'essential pentosuria']",0111258,260800,2843,C0268162,"['-0.2683', '0.462', '-0.341', '-0.03195', '-0.005226', '-0.095', '-0.2422', '0.556', '-0.2019', '0.2291', '-0.2015', '-0.015594', '0.006985', '0.07306', '-0.004898', '0.04105', '-0.0788', '-0.05585', '-0.2076', '-0.4734', '-0.03525', '-0.1925', '0.6504', '0.01269', '0.017', '0.005375', '0.2479', '-0.0343', '-0.1642', '0.1824', '0.3032', '-0.2732', '-0.1512', '-0.01557', '-0.2576', '0.1293', '0.1744', '-0.0429', '0.1307', '-0.1409', '-0.06256', '-0.5864', '0.211', '-0.4456', '-0.2573', '-0.1243', '0.1895', '0.001054', '0.0308', '0.2742', '0.03093', '-0.0673', '-0.295', '-0.322', '0.0761', '-0.141', '0.7524', '-0.2318', '-0.2744', '0.05148', '0.2554', '0.05072', '0.02455', '-0.067', '0.3445', '0.0698', '0.2489', '-0.2903', '-0.2954', '0.0451', '-0.01123', '0.05444', '-0.122', '-0.0858', '0.02397', '0.3315', '-0.04282', '0.0524', '-0.214', '-0.3167', '0.3914', '-0.1687', '0.03665', '-0.02472', '0.211', '-0.00782', '-0.1096', '0.1726', '0.382', '0.0684', '0.335', '-0.1241', '-0.1692', '-0.19', '0.4365', '0.02727', '0.147', '-0.682', '-0.2864', '0.02292']",,,C536652,271.8,,10064170,
mondo:0009847,"pericardial effusion, chronic","['pericardial effusion (disease), chronic', 'pericardial effusion, chronic', 'cholesterol pericarditis']",,260900,,C1850039,,,,C564895,,,,
mondo:0009848,dissecting cellulitis of the scalp,"['perifolliculitis capitis ABSCEDENS ET SUFFODIENS, familial', 'dissecting cellulitis of the scalp']",,260910,345,C0263506,,,,C562486,704.8,,10056961,
mondo:0009849,hyperimmunoglobulinemia D with periodic fever,"['HIDS', 'hyperimmunoglobulinemia D and periodic fever syndrome', 'periodic fever Dutch type', 'hyperimmunoglobulinemia D syndrome', 'periodic fever, Dutch type', 'hyperimmunoglobinemia D with recurrent fever', 'partial mevalonate kinase deficiency', 'hyper-IgD syndrome', 'hyper IgD syndrome']",,260920,343,C0398691,"['0.2583', '0.512', '-0.3813', '0.4692', '0.2023', '-0.2703', '-0.03827', '0.4414', '-0.4585', '-0.1438', '0.4116', '0.2394', '0.1904', '0.4517', '-0.443', '0.2617', '-0.1339', '-0.2727', '-0.1079', '-0.162', '-0.008064', '-0.3708', '0.02086', '-0.1643', '-0.329', '-0.3706', '-0.3604', '0.3484', '-0.4653', '0.12445', '-0.1047', '-0.2397', '-0.06113', '-0.2487', '-0.1677', '0.629', '-0.75', '-0.05798', '-0.006298', '-0.2725', '-0.05124', '-0.4167', '-0.1632', '-0.862', '0.5557', '0.1726', '-0.4646', '-0.2542', '-0.495', '0.9536', '-0.988', '0.1824', '0.3347', '0.3376', '-0.0769', '0.5137', '-0.4556', '0.2224', '-0.2566', '-0.0783', '0.3438', '-0.01423', '0.0088', '-0.0453', '0.454', '-0.1361', '0.5664', '0.2323', '-0.211', '0.553', '-0.3735', '0.5034', '-0.2028', '-0.6787', '0.389', '0.831', '-0.132', '0.2827', '0.4448', '-0.2306', '0.05493', '-0.0307', '0.04303', '0.1065', '0.3223', '-0.2216', '-0.09357', '0.5884', '0.347', '0.1776', '0.2593', '-0.04837', '0.0951', '0.1641', '0.4192', '0.4517', '0.1925', '-0.7007', '-0.011635', '-0.593']",,,,,,,
mondo:0009850,"periodontitis, chronic, adult","['periodontitis, adult', 'periodontitis, chronic']",,260950,,C0266929,,,,,,,,
mondo:0009851,"peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain","['peripheral neuropathy, ataxia, focal necrotizing encephalopathy, and spongy degeneration of brain']",,260970,,C1850022,,,,C564894,,,,
mondo:0009852,hereditary intrinsic factor deficiency,"['pernicious Anemia, congenital, due to defect of intrinsic Factor', 'gastric intrinsic factor deficiency', 'intrinsic factor, congenital deficiency of', 'congenital pernicious anemia due to defect of intrinsic factor', 'hereditary juvenile megaloblastic anaemia due to intrinsic factor deficiency', 'hereditary juvenile megaloblastic anemia due to intrinsic factor deficiency', 'congenital pernicious anaemia due to defect of intrinsic factor', 'intrinsic factor deficiency', 'IFD', 'congenital pernicious anaemia', 'congenital intrinsic factor deficiency', 'congenital pernicious anemia']",0050734,261000,332,C1394891,"['-0.00872', '-0.1443', '-0.005512', '-0.261', '-0.1449', '0.05057', '-0.1407', '0.4546', '-0.2113', '-0.4524', '-0.276', '0.206', '-0.0931', '0.4248', '0.2292', '-0.502', '0.2122', '-0.2046', '-0.2239', '-1.099', '0.2278', '-0.447', '-0.0592', '-0.3994', '-0.02814', '-0.2676', '-0.06726', '0.02133', '-0.4177', '-0.4324', '-0.2715', '-0.0545', '-0.013756', '-0.0518', '-0.1936', '0.2212', '-0.01246', '-0.794', '0.02208', '0.647', '-0.4607', '-0.471', '0.046', '0.1527', '0.2942', '0.0965', '-0.0992', '0.3467', '-0.4631', '-0.0704', '0.3684', '0.1608', '0.1859', '0.1096', '-0.1649', '-0.1648', '0.3506', '0.2118', '-0.418', '0.342', '0.2186', '0.4658', '0.02217', '-0.2837', '0.1825', '-0.01232', '0.135', '0.2499', '-0.3696', '-0.1707', '0.066', '-0.2576', '-0.4976', '-0.548', '0.712', '0.581', '0.2452', '-0.6807', '0.2883', '0.02342', '0.2913', '-0.4045', '0.2058', '0.2793', '0.1356', '-0.1261', '0.006733', '0.573', '0.5557', '-0.3018', '0.461', '0.2527', '0.1926', '-0.4583', '0.5635', '0.664', '0.55', '0.02124', '-0.1691', '-0.0923']",,,C563242,281.3,,10070440,
mondo:0009853,Imerslund-Grasbeck syndrome,"['familial megaloblastic anemia', 'juvenile megaloblastic Anemia', 'selective cobalamin malabsorption with proteinuria', 'juvenile megaloblastic Anaemia', 'Imerslund-Gräsbeck syndrome', 'Imerslund-Grasbeck syndrome', 'defect of enterocyte intrinsic factor receptor', 'enterocyte cobalamin malabsorption', 'familial megaloblastic anaemia', 'Gräsbeck-Imerslund disease']",,,35858,,"['0.3079', '0.3708', '-0.06476', '0.00752', '-0.2896', '-0.1041', '-0.4392', '0.679', '0.04645', '-0.59', '0.06046', '0.268', '-0.1793', '0.4666', '-0.1788', '-0.12036', '0.12103', '-0.07855', '-0.182', '-0.577', '0.08844', '-0.5415', '0.2605', '-0.1903', '0.1736', '0.03882', '-0.2347', '0.4524', '0.0603', '-0.3665', '0.1295', '0.139', '0.2368', '0.2542', '-0.11127', '0.0513', '-0.1049', '-0.3396', '0.01041', '0.776', '-0.22', '-0.2715', '0.609', '-0.2498', '0.1549', '-0.2805', '0.2137', '-0.3853', '-0.2114', '0.02657', '-0.18', '-0.3438', '-0.057', '-0.4558', '0.1119', '-0.04587', '0.3643', '0.02995', '-0.5347', '0.4148', '0.5757', '-0.05234', '0.375', '-0.1917', '0.2886', '0.0716', '0.7935', '0.0856', '-0.1511', '0.3782', '0.3906', '-0.265', '-0.4253', '-0.148', '0.2026', '0.2356', '0.236', '-0.1993', '-0.3035', '0.23', '0.249', '-0.3313', '0.0537', '0.4229', '0.2095', '-0.01096', '0.03296', '0.125', '0.604', '-0.005062', '0.578', '0.2002', '-0.0387', '-0.1963', '0.463', '0.4858', '-0.2537', '-0.3052', '0.194', '0.08765']",,,C538556,281.3,,,
mondo:0009854,"peroneus tertius muscle, absence of","['peroneus tertius muscle, absence of']",,261400,,,,,,,,,,
mondo:0009855,d-bifunctional protein deficiency,"['D-bifunctional enzyme deficiency', '17-beta-hydroxysteroid dehydrogenase 4 deficiency', '17-beta-hydroxysteroid dehydrogenase IV deficiency', 'DBP deficiency', 'HSD17B4 deficiency', 'pseudo-Zellweger syndrome', 'Pbfe deficiency', 'bifunctional enzyme deficiency', 'peroxisomal multifunctional enzyme deficiency', 'multifunctional enzyme deficiency', 'peroxisomal bifunctional enzyme deficiency', 'peroxisomal multifunctional enzyme (MFE2) deficiency', 'd-bifunctional protein deficiency']",0090031,261515,300,CN203333,"['0.1903', '0.1984', '-0.04675', '0.08435', '0.3232', '-0.5464', '-0.2766', '0.06256', '-0.575', '0.1377', '-0.10236', '-0.3657', '0.442', '0.10815', '-0.3018', '0.04977', '-0.04248', '-0.04413', '-0.474', '-0.1334', '-0.3167', '-0.05457', '0.749', '-0.06235', '0.1274', '-0.3374', '-0.1342', '0.2197', '-0.3784', '0.1912', '0.762', '0.1965', '0.7144', '0.207', '0.0758', '-0.3638', '-0.2485', '0.1614', '0.2249', '-0.1874', '0.0001911', '-0.3977', '-0.03317', '0.3015', '-0.1309', '-0.1853', '0.5117', '0.1558', '-0.02162', '0.128', '0.0825', '-0.6616', '-0.1738', '-0.02199', '-0.0568', '-0.3062', '0.014755', '-0.001762', '-0.05988', '0.4321', '-0.0307', '0.00427', '0.6235', '0.2722', '-0.233', '0.0946', '0.11316', '-0.2218', '-0.6157', '-0.1537', '0.005524', '0.2177', '-0.07056', '0.4285', '0.3599', '0.9473', '0.3335', '-0.224', '-0.3286', '-0.02208', '0.258', '-0.03067', '-0.339', '0.03415', '-0.2622', '0.595', '-0.5024', '0.05084', '0.8867', '0.1896', '-0.1719', '0.3845', '-0.2252', '0.333', '0.397', '0.514', '0.02774', '-0.0992', '0.68', '0.1636']",C119676,,,277.6,,,
mondo:0009856,Peters plus syndrome,"['Peters anomaly with short limb dwarfism', 'Peters anomaly with short-limb dwarfism', 'Peters-plus syndrome', 'Peters anomaly-short limb dwarfism syndrome', 'Krause-Kivlin syndrome', 'Krause-van Schooneveld-Kivlin syndrome']",0080201,261540,709,C0796012,"['-0.1886', '-0.1278', '0.6523', '-0.79', '0.2773', '-0.1411', '0.2233', '0.0904', '-0.1426', '-1.039', '-0.02962', '-0.9165', '-0.04114', '-0.06235', '-0.9565', '-0.818', '-0.515', '-0.04608', '-0.1307', '-0.703', '-0.0645', '0.4011', '0.2103', '-0.3105', '0.2925', '0.1556', '-0.5283', '0.2778', '1.061', '0.000986', '0.432', '0.2656', '0.414', '0.2583', '-0.003431', '-0.529', '-0.3005', '0.0364', '0.0308', '-0.6284', '0.2104', '-0.3328', '0.2827', '0.335', '0.1624', '-0.3552', '0.3206', '0.659', '0.4763', '-0.1924', '-0.5293', '0.3164', '-0.4082', '-0.6904', '-0.2257', '-0.8306', '0.1224', '-0.1992', '-0.3193', '0.128', '0.192', '0.03253', '-0.0859', '0.302', '-0.2377', '-0.607', '0.358', '0.4075', '-0.5317', '0.1361', '-0.3245', '0.2576', '0.529', '0.2494', '-0.342', '0.2274', '0.0727', '-0.3477', '-0.424', '0.00432', '0.02759', '0.4949', '0.4177', '0.5156', '-0.02171', '0.03357', '0.3372', '-0.2335', '0.1233', '0.356', '0.1187', '0.2795', '0.2627', '0.3164', '1.401', '0.3706', '0.595', '-0.03574', '0.2467', '0.632']",C123436,,C537617,743.44,,,
mondo:0009857,persistent Mullerian duct syndrome,"['persistent Muellerian duct syndrome', 'female genital ducts in otherwise normal male', 'persistent mullerian duct syndrome, types 1 and 2', 'PMDS', 'persistent MULLERIAN duct syndrome, types I and II', 'persistent mullerian duct syndrome, type I', 'pseudohermaphroditism, Male internal', 'persistent oviduct syndrome', 'persistent Mullerian derivatives', 'hernia uteri inguinale', 'persistent Müllerian duct syndrome', 'female genital ducts in otherwise normal Male', 'persistent Müllerian derivatives', 'persistent mullerian duct syndrome, type II']",0050791,261550,2856,C1849930,"['-0.258', '-0.10944', '0.04764', '-0.3887', '0.3992', '-0.4314', '0.3591', '0.4443', '-0.1307', '-1.065', '0.03445', '-0.3638', '-0.3074', '0.587', '-0.2554', '-0.0246', '0.002079', '0.2893', '-0.5107', '-0.3982', '-0.4705', '0.04758', '0.6895', '-0.3032', '0.6694', '-0.4194', '0.2676', '0.3013', '0.1245', '-0.1476', '0.9766', '-0.0891', '0.2142', '0.1056', '0.2177', '0.104', '0.0211', '0.01304', '-0.2295', '-0.4119', '0.685', '0.2', '-0.1948', '-0.1255', '-0.1488', '-0.05875', '0.0837', '0.03119', '0.0897', '0.116', '-0.073', '-0.3965', '-0.04382', '-0.209', '-0.8115', '0.5884', '-0.1323', '-0.3115', '-0.8916', '0.3496', '0.544', '0.652', '0.3926', '0.03116', '0.00422', '-0.2026', '0.8965', '-0.013916', '-0.0494', '0.2106', '-0.3374', '0.0458', '-0.4043', '0.2744', '0.0638', '-0.02', '-0.1194', '0.2362', '-0.6455', '-0.4688', '0.1129', '0.3203', '0.1914', '-0.1754', '-0.01529', '-0.282', '0.3657', '-0.1819', '-0.10803', '-0.851', '-0.3481', '0.9067', '-0.297', '0.1439', '0.3906', '-0.3733', '0.31', '-0.9136', '-0.8057', '0.4802']",C120188,,C536665,752.89,,,
mondo:0009858,Pfeiffer-Palm-Teller syndrome,"['short stature, unique facies, enamel hypoplasia, progressive Joint stiffness, and high-pitched voice', 'Pfeiffer-Palm-Teller syndrome', 'PPT syndrome', 'Pfeiffer Palm Teller syndrome', 'short stature unique facies enamel hypoplasia progressive joint stiffness and high-pitched voice']",,261560,2871,C1849929,,,,C537889,,,,
mondo:0009859,PHAVER syndrome,"['PHAVER syndrome', 'Powell-Chandra-Saal syndrome', 'pterygia heart defects autosomal recessive inheritance vertebral defects Ear anomalies and radial defects']",,261575,2876,C1849928,,,,C538357,,,,
mondo:0009860,phenformin 4-hydroxylation,['phenformin 4-hydroxylation'],,261590,,,,,,,,,,
mondo:0009861,phenylketonuria,"['phenylalaninemia', 'PKU', 'PAH deficiency', 'phenylketonuria', 'phenylketonuria, maternal', 'oligophrenia Phenylpyruvica', 'HPA, non-PKU mild', 'hyperphenylalaninemia, non-PKU mild', 'phenylalanine hydroxylase deficiency']",9281,261600,716,C0031485,"['0.1519', '0.1829', '0.584', '-0.11646', '0.134', '-0.725', '-0.666', '0.5522', '0.2878', '0.2144', '-0.01021', '-0.10455', '0.2515', '0.7505', '-0.2893', '-0.5483', '-0.1277', '0.06396', '-0.603', '-0.316', '-0.311', '-0.41', '0.324', '-0.11475', '-0.08386', '-0.821', '-0.2898', '0.5317', '0.2778', '-0.3037', '0.5537', '-0.4558', '0.495', '0.244', '-0.505', '-0.04504', '-0.3281', '0.407', '0.5312', '-0.2166', '0.1766', '-0.5205', '-0.43', '-0.507', '-0.3828', '-0.3335', '0.1652', '-0.1873', '0.11346', '0.537', '0.519', '-0.2251', '-0.09814', '-0.3618', '-0.0866', '0.3206', '-0.2072', '0.792', '-0.02292', '0.2922', '-0.5503', '0.2072', '0.513', '0.1827', '-0.04465', '0.6313', '0.02858', '0.6636', '-0.835', '0.0807', '0.4238', '0.276', '-0.2747', '0.02995', '-0.6055', '0.4954', '0.1511', '-0.3347', '-0.31', '-0.1929', '0.568', '-0.4702', '-0.6123', '0.391', '0.3694', '0.0821', '0.01903', '-0.3552', '0.7085', '0.867', '0.4912', '0.276', '-0.1814', '-0.2491', '0.10345', '0.3828', '0.04874', '-0.963', '0.006477', '-0.2234']",C81315,,D010661,270.1,,10034872,
mondo:0009862,dihydropteridine reductase deficiency,"['dihydropteridine reductase deficiency', 'hyperphenylalaninemia, BH4-deficient C', 'hyperphenylalaninemia due to dihydropteridine reductase deficiency', 'DHPR deficiency', 'hyperphenylalaninemia, BH4-deficient, C', 'hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to DHPR deficiency', 'disorder of 6,7-dihydropteridine reductase activity', '6,7-dihydropteridine reductase activity disease', 'PKU type 2', 'hyperphenylalaninemia, Bh4-deficient, type C', 'hyperphenylalaninemia, BH-4-deficient, C', 'quinoid dihydropteridine reductase deficiency', 'HPABH4C', 'Qdpr deficiency', 'phenylketonuria type 2']",0081130,261630,226,,"['-0.65', '0.4404', '0.7163', '-0.4443', '0.0698', '-0.1636', '-0.06287', '0.549', '-0.4744', '-0.4995', '-0.5576', '-0.2416', '0.08954', '0.1378', '0.4116', '-0.09937', '-0.3213', '-0.452', '-0.533', '-0.8076', '0.1345', '-0.2407', '0.4097', '0.1346', '-0.3984', '0.4487', '0.365', '0.1608', '-0.555', '0.01639', '-0.04956', '0.2256', '0.4885', '0.1984', '-0.317', '0.2014', '-0.1577', '-0.03232', '0.00811', '-0.2072', '0.3184', '-0.2803', '0.3333', '-0.0871', '-0.127', '-0.01166', '0.3784', '-0.1783', '0.1655', '0.6167', '0.1354', '-0.1096', '-0.2383', '-0.7466', '0.2142', '0.2157', '0.545', '-0.1855', '-0.4277', '0.2866', '-0.343', '0.533', '0.293', '-0.339', '0.4014', '0.1918', '0.6504', '-0.1869', '-0.508', '-0.1438', '0.1538', '0.4468', '-0.1957', '0.11084', '0.2126', '1.047', '0.729', '-0.5454', '-0.38', '0.004204', '0.0596', '-0.09436', '0.3645', '0.417', '0.477', '0.02815', '0.00782', '0.0639', '0.556', '0.009155', '0.1987', '0.3992', '-0.385', '-0.1365', '0.2556', '0.8413', '-0.2761', '-0.1682', '-0.0666', '-0.2037']",C138173,,,,,,
mondo:0009863,BH4-deficient hyperphenylalaninemia A,"['hyperphenylalaninemia, Bh4-deficient, type a', 'hyperphenylalanemia, BH4-deficient, A', 'hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to PTS deficiency', 'HPABH4A', 'Bh4-deficient hyperphenylalaninemia type A', 'PTS deficiency hyperphenylalaninemia, BH4-deficient, due to partial PTS deficiency, included', 'hyperphenylalaninemia due to 6-pyruvoyl-tetrahydropterin synthase deficiency', 'hyperphenylalaninemia, BH4-deficient, type A', '6-pyruvoyl-tetrahydropterin synthase deficiency', 'hyperphenylalaninemia, BH4-deficient A', '6-pyruvoyl tetrahydropterin synthase deficiency', 'hyperphenylalaninemia due to 6-pyruvoyltetrahydropterin synthase deficiency', 'PTS deficiency', 'hyperphenylalaninemia, BH4-deficient, A', 'tetrahydobioperin-deficient hyperphenylalaninemia due to PTS deficiency', 'hyperphenylalaninemia, Bh4-deficient, due to partial PTS deficiency']",0090106,261640,13,C0878676,"['-0.6265', '0.425', '0.4153', '-0.1754', '0.0764', '-0.1869', '-0.0373', '0.345', '-0.3818', '0.01254', '0.002901', '0.3494', '0.10565', '0.07904', '0.09937', '-0.01633', '-0.03497', '-0.425', '-0.807', '-0.7334', '0.05273', '-0.09735', '-0.1249', '0.1765', '-0.08984', '0.2869', '0.2466', '0.07886', '-0.61', '0.2744', '-0.1229', '0.4922', '0.3025', '0.199', '-0.253', '-0.1841', '0.05017', '-0.3147', '0.10333', '-0.2888', '0.3555', '-0.0909', '0.02417', '-0.0672', '-0.3398', '-0.3943', '0.246', '-0.394', '0.3157', '0.845', '-0.2305', '-0.1803', '-0.419', '-0.3022', '0.3005', '-0.1138', '0.406', '0.2028', '-0.5234', '0.5166', '0.02469', '0.4805', '0.647', '0.0406', '0.1029', '0.0929', '0.5', '-0.0591', '-0.1306', '0.02684', '-0.2737', '0.03162', '-0.2115', '-0.648', '0.3127', '0.528', '0.185', '-0.1306', '-0.3196', '-0.08374', '0.3718', '0.1298', '0.0507', '-0.0705', '0.2783', '-0.3572', '0.10266', '-0.1761', '0.6846', '0.08563', '-0.0758', '0.2104', '-0.0802', '-0.5664', '0.2375', '1.0', '0.2312', '-0.543', '0.2864', '0.2888']",C138171,,C535325,,,,
mondo:0009864,"phosphoenolpyruvate carboxykinase deficiency, mitochondrial","['PEPCK2', 'PEPCK deficiency, mitochondrial', 'phosphoenolpyruvate carboxykinase deficiency, mitochondrial', 'PEPCK 2 deficiency', 'PEPCK2 deficiency', 'PCKDM', 'phosphoenolpyruvate carboxykinase 2 deficiency', 'PCK2 deficiency']",,261650,79317,C1849821,"['-0.1249', '0.1125', '0.01492', '-0.001965', '0.05768', '-0.1158', '-0.01926', '0.04785', '-0.049', '-0.0371', '-0.067', '0.014465', '0.0261', '-0.000825', '-0.0365', '-0.05405', '-0.0164', '0.004158', '-0.075', '-0.196', '-0.01006', '-0.0805', '0.1276', '-0.02412', '0.02107', '-0.01756', '-0.01237', '-0.0618', '-0.0008945', '-0.1082', '0.0663', '0.0676', '0.0908', '0.0825', '-0.00989', '-0.09357', '0.01365', '-0.0504', '-0.03467', '-0.0853', '0.04865', '-0.1569', '0.06207', '0.01332', '-0.0677', '-0.10046', '0.04184', '0.07196', '0.02141', '0.06757', '-0.000534', '-0.0875', '0.02684', '0.01584', '-0.0975', '-0.05685', '0.12115', '-0.05817', '-0.1499', '0.06183', '0.06146', '0.08575', '0.06033', '-0.00546', '0.02267', '-0.02455', '0.12006', '0.0281', '-0.133', '0.0766', '-0.0764', '0.000789', '0.03165', '-0.1055', '0.072', '0.08344', '0.002384', '-0.0163', '-0.10284', '-0.0635', '0.03882', '-0.0209', '-0.03336', '0.05054', '0.0173', '0.0232', '0.04614', '0.08966', '0.198', '0.00501', '0.08325', '0.09607', '0.02982', '-0.06116', '0.2189', '0.1322', '0.1009', '-0.163', '-0.05734', '0.0289']",,,C564890,,,,
mondo:0009865,glycogen storage disease due to phosphoglycerate mutase deficiency,"['GSD due to phosphoglycerate mutase deficiency', 'GSD10', 'myopathy due to phosphoglycerate mutase deficiency', 'glycogen storage disease X', 'GSD type 10', 'PGAM deficiency', 'Phosphoglycerate mutase, muscle, deficiency of', 'GSDX', 'GSD 10', 'glycogen storage disease caused by mutation in PGAM2', 'PGAM2 glycogen storage disease', 'muscle phosphoglycerate mutase deficiency', 'myopathy due to Phosphoglycerate mutase deficiency', 'PGAMM deficiency', 'glycogen storage disease 10', 'Phosphoglycerate mutase deficiency', 'glycogenosis due to phosphoglycerate mutase deficiency', 'glycogen storage disease type 10']",,261670,97234,,"['-0.3047', '0.05664', '-0.361', '-0.0356', '0.1348', '-0.424', '0.006107', '0.4924', '-0.0645', '-0.1014', '-0.0386', '0.0956', '-0.02382', '-0.1833', '-0.4268', '0.2242', '-0.3562', '-0.1038', '-0.4814', '-0.362', '0.675', '-0.0949', '0.3577', '0.4043', '-0.2329', '0.3513', '0.1066', '-0.3777', '-0.007935', '0.1838', '-0.1022', '0.08716', '0.275', '0.1225', '-0.00421', '-0.506', '-0.2101', '-0.062', '-0.0576', '-0.2402', '-0.1243', '-0.6514', '0.217', '0.1835', '-0.2542', '-0.1611', '0.007053', '0.3127', '-0.1561', '0.4084', '-0.01924', '-0.378', '0.05508', '0.07404', '-0.3623', '-0.5083', '0.4722', '0.2144', '-0.7134', '0.0357', '0.4524', '0.1162', '0.2277', '-0.2646', '-0.3828', '-0.01555', '-0.0588', '0.2222', '-0.4368', '-0.02249', '0.01907', '-0.1885', '-0.003265', '0.4385', '0.797', '0.5225', '0.3225', '0.01012', '-0.518', '0.02272', '0.2737', '-0.1169', '0.5664', '-0.3147', '0.2013', '0.2361', '0.07806', '0.539', '0.2384', '-0.2986', '0.8286', '-0.1505', '0.12274', '-0.2915', '0.6587', '0.877', '0.2158', '-0.7046', '-0.1783', '0.0639']",C131647,,C536176,,,,
mondo:0009866,"phosphoenolpyruvate carboxykinase deficiency, cytosolic","['PEPCK deficiency, cytosolic', 'phosphoenolpyruvate carboxykinase deficiency', 'PCKDC', 'phosphoenolpyruvate carboxylase deficiency', 'PCK1 deficiency, cytosolic', 'phosphoenolpyruvate carboxykinase deficiency, cytosolic', 'PEP carboxykinase deficiency', 'phosphopyruvate carboxylase deficiency', 'phosphoenolpyruvate carboxykinase-1 (PCK1) deficiency', 'PEPCK 1 deficiency']",,261680,79316,,"['-0.05673', '0.0476', '-0.004276', '-0.008156', '0.02232', '-0.0555', '0.006424', '0.03516', '-0.02744', '-0.01949', '-0.01547', '0.001431', '0.00989', '0.000446', '-0.02974', '-0.00666', '-0.007202', '-0.02133', '-0.03497', '-0.07306', '-0.003838', '-0.01897', '0.05698', '-0.01304', '0.01566', '-0.010704', '0.011055', '-0.0195', '0.000279', '-0.0363', '0.0353', '0.02515', '0.03293', '0.0188', '0.0009646', '-0.03867', '-0.004097', '-0.00854', '-0.012344', '-0.04926', '0.015366', '-0.06192', '0.02333', '-3.2e-06', '-0.02217', '-0.05', '0.006935', '0.032', '0.011856', '0.0386', '-0.01271', '-0.02438', '-0.003428', '0.0211', '-0.02429', '-0.033', '0.0631', '-0.0231', '-0.05472', '0.02312', '0.03168', '0.03534', '0.01304', '-0.0003169', '0.00849', '0.001933', '0.0542', '0.012695', '-0.04117', '0.03317', '-0.02188', '0.0117', '0.00726', '-0.02066', '0.01599', '0.04056', '0.00479', '-0.01376', '-0.0168', '-0.01929', '0.01703', '0.005474', '-0.005474', '0.03183', '0.0162', '0.00796', '0.006622', '0.0379', '0.0735', '0.006683', '0.02986', '0.03091', '-0.001769', '-0.006187', '0.0885', '0.05035', '0.03403', '-0.06476', '-0.0117', '0.011055']",,,,,,,
mondo:0009867,lethal congenital glycogen storage disease of heart,"['fatal congenital hypertrophic cardiomyopathy due to glycogenosis', 'fatal congenital hypertrophic cardiomyopathy due to glycogen storage disease', 'fatal congenital nonlysosomal cardiac glycogenosis', 'PRKAG2 glycogen storage disease', 'glycogen storage disease of heart, lethal congenital', 'phosphorylase kinase deficiency of heart', 'glycogen storage disease of heart', 'fatal congenital hypertrophic cardiomyopathy due to GSD', 'glycogen storage disease caused by mutation in PRKAG2']",0090101,261740,439854,C1849813,"['-0.0538', '0.09607', '0.01642', '0.032', '0.0695', '-0.113', '0.01479', '0.1052', '-0.05222', '-0.02943', '-0.01556', '-0.01401', '-0.01837', '-0.000773', '-0.05847', '-0.05908', '-0.03833', '-0.0431', '-0.0906', '-0.1656', '0.02966', '-0.0348', '0.12', '-0.0177', '-0.01979', '-0.0235', '-0.00671', '-0.01805', '0.01779', '-0.02', '0.0929', '-0.01522', '0.1027', '0.03662', '0.001529', '-0.087', '0.002625', '-0.00873', '0.00684', '-0.06635', '-0.02246', '-0.08746', '0.03687', '0.04163', '-0.04147', '-0.06122', '0.00943', '0.10706', '-0.036', '0.06647', '-0.05173', '-0.02751', '0.05887', '-0.02547', '-0.0681', '-0.10767', '0.0816', '-0.01538', '-0.09235', '-0.012115', '0.07446', '0.02234', '0.03033', '-0.0193', '-0.02646', '-0.00588', '0.0756', '0.076', '-0.1359', '0.0605', '-0.095', '0.0012865', '0.02135', '-0.00936', '0.0471', '0.0514', '0.010895', '0.02943', '-0.09357', '-0.06604', '-0.02614', '0.000758', '-0.0457', '0.03952', '0.01452', '0.0163', '0.0867', '0.05554', '0.11426', '0.011475', '0.0508', '0.0717', '0.04474', '0.01773', '0.1891', '0.0728', '0.1229', '-0.1127', '-0.001617', '0.03296']",,,C564888,,,,
mondo:0009868,glycogen storage disease IXb,"['GSD9B', 'glycogen storage disease type IXb', 'glycogen storage disease caused by mutation in PHKB', 'phosphorylase kinase deficiency of liver and muscle, autosomal recessive', 'glycogen storage disease type 9B', 'glycogen storage disease due to liver and muscle phosphorylase kinase deficiency', 'GSD IXb', 'GSD type IXb', 'glycogenosis type 9B', 'glycogenosis type IXb', 'glycogenosis of liver and muscle, autosomal recessive', 'PHKB glycogen storage disease', 'GSD type 9B', 'glycogen storage disease IXb', 'PHKB-related glycogen storage disease type IX', 'GSD due to liver and muscle phosphorylase kinase deficiency', 'glycogenosis due to liver and muscle phosphorylase kinase deficiency']",0111041,261750,79240,C0543514,"['-0.6025', '-0.05826', '-0.1276', '0.1595', '0.258', '-0.4553', '-0.0777', '0.6494', '-0.1076', '0.2588', '0.1038', '-0.0566', '-0.06555', '0.36', '0.10004', '-0.2412', '-0.2922', '-0.4106', '-0.809', '-0.7627', '0.2444', '-0.4463', '0.6885', '0.1571', '-0.47', '-0.412', '0.1132', '-0.4697', '-0.03204', '0.2269', '0.1182', '0.1814', '0.256', '0.4492', '-0.00928', '-0.343', '-0.1997', '0.1414', '0.3564', '0.2129', '0.3237', '-0.4202', '0.1624', '0.5225', '-0.52', '0.1995', '-0.1885', '0.1418', '0.0593', '0.6963', '0.2034', '-0.495', '0.523', '-0.1207', '-0.2076', '-0.6304', '0.1056', '0.2252', '-0.2515', '0.08875', '0.09735', '-0.2056', '0.5', '-0.432', '-0.2761', '0.3086', '0.521', '0.1638', '-0.547', '-0.09064', '0.01424', '-0.3718', '0.337', '0.0552', '0.567', '0.4424', '0.327', '-0.08716', '-0.239', '0.258', '-0.5166', '0.07587', '-0.06555', '-0.465', '0.4385', '0.2866', '0.3435', '-0.1902', '0.767', '0.3174', '0.3228', '0.409', '-0.09924', '-0.321', '0.559', '0.5757', '0.3684', '-0.428', '0.07886', '0.07465']",,,C563008,,,,
mondo:0009869,isolated Pierre-Robin syndrome,"['Pierre-Robin syndrome', 'isolated Pierre Robin sequence', 'Pierre Robin sequence', 'glossoptosis, micrognathia, and cleft palate', 'syndrome, Pierre Robin', 'syndrome, Pierre-Robin', 'Robin syndrome, Pierre', 'sequence, Pierre Robin^s', 'Pierre Robins sequence', 'Pierre Robin syndrome', 'PRBNS', 'isolated Pierre Robin syndrome', 'sequence, Pierre Robin', 'sequence, Robin', 'Pierre Robin^s sequence', 'Pierre Robin syndrome skeletal dysplasia polydactyly', 'Robin sequence']",,261800,718,,,C85010,,D010855,,,,
mondo:0009870,pili torti,"['pili torti', 'pili torti, Ronchese type', 'pili torti (disease)', 'twisted hair', 'pili torti, early-onset', 'coarse, dry, lusterless hair which breaks off easily']",,261900,2889,,,,,C562485,,,,0003777
mondo:0009871,pili torti-developmental delay-neurological abnormalities syndrome,"['pili torti developmental delay neurological abnormalities', 'pili torti and developmental delay', 'abnormal hair, joint laxity, and developmental delay']",,261990,2891,C1849811,"['-0.1954', '0.3096', '0.1643', '-0.1588', '0.1404', '-0.3716', '-0.3147', '0.538', '-0.08246', '-0.194', '-0.01368', '-0.2128', '0.0696', '-0.1875', '0.1338', '0.03061', '0.1293', '-0.10077', '-0.3225', '-0.3967', '-0.2216', '0.03668', '0.1768', '-0.512', '0.2366', '-0.1647', '-0.3135', '0.1403', '0.2041', '-0.453', '0.1877', '-0.211', '0.1964', '0.1106', '-0.0647', '-0.01087', '-0.0458', '-0.496', '-0.01875', '-0.2319', '0.2421', '-0.1459', '-0.225', '-0.2017', '0.04913', '0.0581', '-0.1195', '-0.002197', '-0.259', '-0.2191', '-0.28', '-0.08936', '-0.0748', '-0.02515', '0.03091', '-0.05914', '0.108', '0.09076', '-0.1428', '0.2668', '0.2837', '0.013725', '-0.006016', '0.1796', '-0.03156', '0.06934', '-0.02621', '0.1494', '-0.6533', '0.242', '-0.01889', '0.2173', '0.007545', '-0.03796', '-0.03864', '-0.1337', '0.1006', '-0.1175', '-0.0693', '0.0427', '0.1996', '0.1887', '0.02115', '0.3723', '0.0832', '0.11053', '0.0998', '0.4202', '0.3953', '0.2776', '0.1826', '0.3962', '-0.03348', '0.0958', '0.502', '0.003893', '0.11334', '-0.6143', '0.1735', '0.00997']",,,C537398,,,,
mondo:0009872,Bjornstad syndrome,"['PTD', 'BJS', 'deafness-pili torti-hypogonadism syndrome', 'deafness and pili torti, Bjornstad type', 'pili torti-sensorineural hearing loss', 'BJörnstad syndrome', 'PTND', 'Bjornstad syndrome', 'pili torti and nerve deafness']",0050677,262000,123,C0266006,"['-0.3574', '0.5103', '-0.02249', '0.2812', '0.286', '-0.773', '-0.3887', '0.936', '-0.2417', '-0.645', '-0.12274', '0.1393', '-0.1648', '0.0455', '-0.2776', '-0.2341', '0.396', '0.1165', '-0.03693', '-0.347', '-0.05103', '-0.4116', '-0.11975', '-0.2705', '1.036', '0.3862', '-0.4604', '0.2532', '0.2382', '0.02008', '0.2347', '-0.10803', '-0.612', '0.2046', '0.1355', '0.4607', '0.2856', '-0.4001', '0.1116', '0.11816', '0.0817', '0.0535', '0.0398', '-0.0712', '-0.1702', '-0.3433', '-0.2952', '-0.02966', '0.1521', '-0.3982', '0.04727', '-0.1368', '-0.1481', '0.09106', '0.1715', '-0.3682', '0.4678', '0.0735', '0.04398', '0.03833', '-0.1797', '0.523', '-0.2844', '-0.1843', '-0.4502', '-0.3503', '0.0309', '0.3093', '-0.8594', '0.729', '-0.01517', '-0.2037', '0.37', '0.2563', '0.1638', '-0.0235', '-0.354', '0.4644', '-0.327', '0.2185', '0.4019', '-0.2725', '0.3755', '0.274', '0.1181', '0.05304', '0.41', '0.4429', '0.1781', '1.144', '0.3552', '0.506', '0.3262', '0.526', '1.171', '0.06885', '0.4812', '-0.8696', '0.2927', '-0.01214']",,0002779,C537633,,,,
mondo:0009873,pilodental dysplasia-refractive errors syndrome,"['Trichodental dysplasia with hyperopia', 'PILODENTAL dysplasia with refractive errors', 'Euhidrotic ectodermal dysplasia', 'Kopysc-Barczyk-Krol syndrome']",,262020,2892,C1849805,,,,C535763,,,,
mondo:0009874,Rabson-Mendenhall syndrome,"['pineal hyperplasia, insulin-resistant diabetes mellitus, and somatic abnormalities', 'Mendenhall syndrome', 'Rabson-Mendenhall syndrome']",,262190,769,C0271695,"['0.0455', '0.5005', '0.03442', '-0.1794', '0.2263', '-0.6055', '0.3896', '0.4443', '-0.1126', '-0.6914', '-0.332', '0.04202', '0.3787', '-0.2705', '-0.7505', '-0.1191', '0.1008', '0.02748', '-0.1206', '-0.8496', '0.2544', '-0.608', '0.554', '-0.10455', '0.1528', '0.5723', '-0.2869', '-0.1512', '0.0654', '-0.9907', '0.731', '0.393', '0.03278', '-0.1205', '-0.3325', '0.468', '-0.001935', '0.1488', '-0.3696', '0.1212', '-0.01103', '-0.306', '-0.1399', '0.296', '0.0918', '-0.4568', '0.2202', '-0.0637', '0.3562', '-0.2217', '0.1156', '0.2407', '0.2837', '0.1799', '-0.285', '-0.319', '0.2325', '-0.3945', '-0.04645', '0.2861', '-0.10895', '0.1614', '-0.1772', '-0.317', '-0.1523', '0.09', '-0.0101', '0.163', '-0.816', '0.1382', '-0.58', '0.0182', '0.8555', '0.367', '0.618', '-0.05518', '-0.1937', '-0.05197', '0.1327', '-0.03455', '0.2385', '0.1471', '-0.1864', '-0.03552', '-0.2712', '0.0993', '0.1882', '0.275', '0.5493', '0.416', '0.2576', '0.2905', '0.648', '-0.1109', '0.1641', '-0.0189', '0.3318', '-0.3684', '0.07227', '0.04626']",C131000,,D056731,259.8,,,
mondo:0009875,achromatopsia 3,"['ACHM1', 'RMCH1', 'achromatopsia type 3', 'RMCH1 (formerly)', 'CNGB3 achromatopsia', 'rod monochromatism 1, formerly', 'rod monochromacy 1', 'rod monochromacy 1, formerly', 'ACHM3', 'ACHM1 (formerly)', 'Rod monochromacy 1 (formerly)', 'Rod monochromatism 1 (formerly)', 'ACHM1, formerly', 'achromatopsia caused by mutation in CNGB3', 'total colorblindness with myopia', 'rod monochromatism 1', 'achromatopsia with myopia', 'achromatopsia 3']",0110008,262300,,C1849792,,,,,,,,
mondo:0009876,isolated growth hormone deficiency type IA,"['IGHD1A', 'congenital isolated growth hormone deficiency type IA', 'pituitary dwarfism 1', 'ILLIG type growth hormone deficiency', 'autosomal recessive isolated growth hormone deficiency', 'IGHD IA', 'congenital IGHD type IA', 'IGHD 1A', 'primordial dwarfism', 'congenital isolated growth hormone deficiency', 'sexual ateleiotic dwarfism', 'congenital isolated GH deficiency type IA', 'Illig-type Growth hormone deficiency', 'Illig-type growth hormone deficiency', 'congenital isolated GH deficiency', 'congenital IGHD', 'Growth hormone deficiency, isolated, autosomal recessive', 'isolated growth hormone deficiency type 1A', 'pituitary dwarfism I', 'growth hormone deficiency, isolated, type IA', 'Growth hormone deficiency, isolated autosomal recessive', 'isolated growth hormone deficiency type IA', 'isolated growth hormone deficiency, type IA', 'isolated Growth hormone deficiency, type 1A', 'non-acquired isolated growth hormone deficiency']",0060873,262400,231662,,"['-0.4954', '0.3425', '-0.01918', '0.0358', '0.6416', '-0.1519', '0.03256', '0.4216', '-0.4136', '-0.349', '-0.1146', '0.4172', '0.4167', '0.0739', '0.1416', '0.05283', '0.2136', '-0.03787', '-0.3123', '-0.629', '-0.09033', '-0.2034', '0.2333', '-0.08795', '0.1993', '0.0978', '-0.08105', '-0.2966', '-0.05368', '-0.2512', '0.3923', '0.252', '0.1046', '-0.07117', '-0.3323', '0.06015', '0.006737', '-0.0656', '-0.1799', '-0.05118', '0.196', '-0.2394', '0.2112', '-0.1048', '-0.1836', '-0.3074', '0.1313', '-0.1202', '0.2278', '0.0393', '0.0186', '-0.3499', '-0.1605', '0.2266', '-0.1562', '-0.2788', '0.0553', '-0.10944', '0.003328', '0.3794', '0.3477', '-0.05862', '-0.01932', '-0.1655', '0.0843', '0.262', '0.202', '0.203', '-0.4973', '-0.0706', '-0.08325', '-0.1162', '0.08026', '-0.274', '0.2993', '-0.02127', '-0.07916', '0.1389', '-0.2825', '-0.1788', '0.0697', '0.1943', '-0.2505', '-0.2404', '-0.12427', '0.1469', '0.3625', '0.1271', '0.529', '0.3748', '-0.1536', '0.443', '-0.261', '-0.258', '0.509', '0.09735', '0.209', '-0.4102', '0.249', '0.01968']",,,C537404,259.4,,,
mondo:0009877,Laron syndrome,"['Growth hormone receptor deficiency', 'primary growth hormone insensitivity', 'short stature due to growth hormone resistance', 'Laron syndrome', 'Laron type pituitary dwarfism I', 'Laron-type isolated somatotropin defect', 'GH receptor deficiency', 'Laron-type dwarfism', 'primary GH resistance', 'primary GH insensitivity', 'Laron dwarfism', 'pituitary dwarfism 2', 'primary growth hormone resistance', 'growth hormone insensitivity syndrome', 'pituitary dwarfism II', 'complete growth hormone insensitivity']",9521,262500,633,,"['-0.4824', '0.02773', '0.14', '-0.638', '0.551', '-0.03918', '-0.2035', '1.073', '-0.4036', '-0.1742', '-0.03488', '0.2874', '0.2458', '0.0057', '-0.0615', '0.4355', '0.587', '-0.0853', '-0.7256', '-0.3975', '0.001875', '-0.723', '0.5835', '-0.4175', '0.2012', '-0.2485', '-0.1859', '-0.4001', '-0.03017', '-0.5063', '0.787', '0.1959', '-0.1437', '-0.01046', '-0.3118', '-0.1646', '0.3503', '-0.214', '0.05084', '-0.249', '-0.0822', '0.0675', '-0.4136', '-0.1482', '0.3542', '-0.1901', '0.0825', '-0.01787', '-0.1181', '0.1344', '-0.1633', '-0.7266', '0.279', '0.5586', '-0.4805', '0.4202', '0.2241', '-0.709', '0.3784', '0.4565', '0.1323', '1.03', '-0.0859', '-0.641', '0.5186', '0.2844', '0.363', '0.3162', '-0.1238', '0.0705', '-0.1074', '0.324', '0.1337', '0.11774', '0.166', '-0.0937', '-0.0929', '-0.417', '0.01303', '0.1544', '0.3547', '-0.2527', '0.01883', '0.466', '-0.5737', '0.6587', '0.03757', '-0.3418', '1.171', '0.2327', '-0.1758', '0.6597', '0.527', '0.002796', '0.4631', '-0.0736', '0.06305', '-0.6294', '0.1384', '-0.1304']",C130994,,D046150,,,,
mondo:0009878,"pituitary hormone deficiency, combined, 2","['Hanhart dwarfism', 'pituitary hormone deficiency, combined, 2', 'PROP1 combined pituitary hormone deficiencies, genetic form', 'combined pituitary hormone deficiencies, genetic form caused by mutation in PROP1', 'pituitary hormone deficiency, combined, type 2', 'CPHD2', 'panhypopituitarism', 'ateliotic dwarfism with hypogonadism', 'pituitary dwarfism 3']",,262600,,C0878683,,,,C563172,,,,
mondo:0009879,short stature due to growth hormone qualitative anomaly,"['Biodefective Growth hormone', 'Kowarski syndrome', 'pituitary dwarfism with normal immunoreactive Growth hormone and Low Somatomedin', 'KOWARSKI syndrome']",,262650,629,C1849779,"['-0.9585', '0.1581', '0.12415', '-0.3', '0.282', '0.1372', '0.0245', '0.701', '-0.1489', '-0.5864', '0.02582', '0.2142', '0.2256', '0.2026', '-0.03766', '0.2778', '0.2778', '0.09015', '-0.6025', '-0.563', '0.11237', '-0.1065', '0.11194', '-0.3306', '0.2815', '-0.05508', '-0.1288', '-0.305', '-0.0754', '-0.3071', '0.582', '-0.3203', '0.25', '0.1204', '-0.3882', '-0.03644', '0.2622', '-0.07776', '0.00879', '-0.2396', '0.336', '0.06195', '0.2856', '-0.3933', '0.16', '-0.4036', '0.1713', '-0.1334', '-0.02538', '-0.1975', '0.1744', '-0.624', '-0.11365', '0.3022', '-0.3333', '0.3699', '0.1046', '-0.4583', '-0.333', '0.4263', '0.02753', '0.0905', '-0.1888', '-0.3596', '0.11176', '-0.06604', '0.0963', '0.0789', '-0.589', '-0.04617', '-0.3628', '0.292', '0.1466', '0.1403', '0.3157', '0.3079', '-0.0007005', '0.06015', '-0.1356', '0.0695', '0.126', '0.2969', '-0.046', '-0.1323', '-0.1948', '0.2754', '0.4812', '0.2228', '0.442', '0.07837', '0.06366', '0.25', '-0.2742', '-0.4348', '0.8174', '0.0989', '0.066', '-0.616', '0.03915', '0.007797']",,,C537505,,,,
mondo:0009880,short stature-pituitary and cerebellar defects-small sella turcica syndrome,"['pituitary hormone deficiency, combined, with or without cerebellar defects', 'pituitary hormone deficiency, combined with or without cerebellar defects', 'short stature, pituitary and cerebellar defects, and small sella turcica', 'short stature, pituitary and cerebellar defects and small sella turcica', 'pituitary hormone deficiency, combined 4', 'CPHD4', 'pituitary hormone deficiency, combined, 4', 'pituitary hormone deficiency, combined, type 4']",,262700,85442,C2678408,"['-0.6353', '0.1481', '0.10095', '-0.1626', '0.1116', '-0.2101', '-0.1177', '0.3381', '-0.2957', '-0.5815', '0.0152', '-0.09015', '-0.1602', '-0.421', '0.0461', '-0.148', '0.1716', '-0.0348', '-0.366', '-0.2515', '0.2161', '-0.069', '0.0622', '-0.348', '0.3926', '-0.1177', '-0.2434', '0.0639', '0.3777', '-0.2126', '0.4944', '-0.1982', '-0.04837', '-0.1598', '0.1198', '-0.0874', '-0.1052', '-0.276', '-0.1615', '-0.4365', '0.2563', '-0.3076', '0.1444', '-0.0891', '0.01949', '-0.2039', '0.1868', '0.3267', '-0.006317', '-0.5996', '0.3877', '-0.0278', '-0.3162', '0.09424', '-0.0871', '-0.3406', '0.5693', '-0.2615', '-0.3684', '0.5845', '0.1483', '0.3108', '-0.1893', '-0.006966', '-0.271', '-0.1874', '0.2025', '0.3687', '-0.4014', '0.07965', '-0.4575', '0.218', '0.2646', '0.02336', '-0.1393', '0.0806', '0.04553', '-0.01991', '-0.0005975', '0.2837', '-0.0839', '0.4087', '-0.1626', '0.3208', '-0.2454', '-0.0099', '0.2214', '0.4194', '0.2463', '-0.2423', '-0.227', '0.4434', '0.1292', '-0.3982', '0.9565', '0.00296', '0.3054', '-0.4663', '0.04523', '0.10376']",,,C567492,,,,
mondo:0009881,pituitary dwarfism with large sella turcica,['pituitary dwarfism with large sella turcica'],,262710,,C0271575,,,,C562705,253.8,,,
mondo:0009882,"plasma clot retraction factor, deficiency of","['plasma clot retraction factor, deficiency of']",,262800,,C1849778,,,,C564885,,,,
mondo:0009883,alpha-2-plasmin inhibitor deficiency,"['plasmin inhibitor deficiency', 'anti-plasmin deficiency, congenital', 'antiplasmin deficiency', 'antiplasmin deficiency, congenital', 'congenital alpha2-antiplasmin deficiency', 'antiplasmin defiency', 'alpha-2-plasmin inhibitor deficiency']",0060601,262850,79,C2752081,"['-1.023', '0.02768', '-0.5376', '-0.5913', '-0.06946', '0.10315', '0.2588', '-0.2319', '0.000761', '-0.07526', '0.1879', '0.812', '0.08563', '-0.497', '-0.1769', '0.14', '-0.08386', '0.1696', '-0.4885', '-1.044', '-0.2676', '0.1561', '0.294', '-0.4355', '-0.1683', '-0.1742', '-0.07587', '-0.2637', '0.2277', '-0.1721', '-0.2622', '0.1187', '-0.03275', '0.6763', '-0.356', '0.09576', '0.05203', '-0.5586', '-0.4636', '-0.4856', '0.331', '-0.648', '0.424', '-0.2864', '0.10846', '-0.4004', '-0.508', '0.3965', '0.5894', '0.4229', '0.4573', '-0.667', '0.01258', '0.531', '-0.2712', '-0.672', '0.54', '0.412', '-0.3584', '0.4985', '0.002129', '-0.02797', '-0.03912', '-0.2896', '0.3345', '0.3223', '0.418', '0.2554', '-0.7607', '0.4753', '-0.546', '0.1451', '0.09906', '-0.2156', '0.377', '0.1865', '0.4353', '0.2457', '0.6675', '-0.1359', '-0.4648', '0.0979', '0.4358', '0.3103', '0.3472', '0.3064', '0.07983', '0.383', '0.8667', '-0.652', '-0.08374', '1.127', '0.4102', '0.3076', '0.5244', '0.513', '0.8125', '-0.5605', '0.0498', '0.2524']",,,C537777,,,,
mondo:0009884,platelet prostacyclin receptor defect,"['platelet prostacyclin receptor defect', 'Vienna-Hietzing defect']",,262875,,C1849774,,,,C564884,,,,
mondo:0009885,Scott syndrome,"['BDPLT7', 'bleeding Abnormality due to deficiency of Platelet binding of Factor 10', 'familial prothrombin conversion defect', 'bleeding disorder, Platelet-type, 7', 'familial prothrombin consumption inhibitor', 'SCTS', 'Platelet factor X receptor deficiency', 'prothrombin consumption inhibitor, familial', 'bleeding abnormality due to deficiency of platelet biding of factor X', 'Scott syndrome', 'prothrombin consumption deficiency', 'platelet-type bleeding disorder 7', 'prothrombin conversion defect, familial']",0111052,262890,806,C0796149,"['-0.3386', '0.0363', '0.09094', '-0.325', '-0.1223', '-0.09174', '-0.0638', '0.2844', '-0.3386', '0.01665', '-0.10706', '0.005787', '0.2556', '-0.3218', '-0.2477', '0.0446', '0.2974', '0.1451', '-0.22', '-0.409', '0.02122', '0.01147', '0.4211', '-0.2693', '0.2141', '-0.1616', '-0.0373', '0.04422', '0.351', '-0.3542', '-0.0491', '0.09705', '0.2412', '0.1394', '-0.00969', '-0.2369', '0.1139', '-0.2465', '-0.00502', '-0.4836', '0.2783', '-0.4614', '-0.003092', '-0.339', '-0.03253', '-0.1862', '-0.0457', '0.5024', '0.134', '0.001767', '-0.197', '-0.1219', '-0.05063', '0.1118', '-0.417', '-0.293', '0.0509', '-0.2554', '-0.1329', '0.1376', '-0.1394', '-0.1381', '0.02325', '-0.1342', '0.04868', '-0.1448', '0.1534', '0.1287', '-0.2937', '0.2598', '-0.5054', '0.1421', '0.2045', '-0.0397', '0.01497', '0.02144', '0.5034', '-0.1812', '-0.0732', '-0.2217', '-0.2112', '0.01993', '0.0991', '0.343', '0.1976', '0.04944', '-0.177', '0.4146', '0.1986', '0.05542', '0.0479', '0.3506', '0.2063', '0.1489', '0.2998', '0.2089', '0.2937', '-0.626', '0.03114', '0.3267']",,,C563120,,,,
mondo:0009886,pleoconial myopathy with salt craving,['pleoconial myopathy with salt craving'],,262900,,C1849773,,,,C564883,,,,
mondo:0009887,desquamative interstitial pneumonia,"['interstitial lung disease, desquamative', 'interstitial pneumonitis, desquamative, familial', 'ILD, desquamative', 'respiratory bronchiolitis interstitial lung disease', 'desquamative interstitial pneumonia', 'RBILD', 'pneumonitis, desquamative interstitial, familial', 'respiratory bronchiolitis-associated interstitial lung disease', 'DIP', 'pneumonia, desquamative interstitial, familial', 'familial desquamative interstitial pneumonitis']",0050158,263000,98852,C0238378,,C35288,,C562470,516.37,,,
mondo:0009888,"polycystic kidney, cataract, and congenital blindness","['polycystic kidney, cataract, and congenital blindness']",,263100,,C1849771,,,,C564882,,,,
mondo:0009889,autosomal recessive polycystic kidney disease,"['polycystic kidney disease, infantile, type I', 'AR-PKD', 'polycystic kidney disease, infantile type', 'ARPKD', 'autosomal recessive polycystic kidney', 'PKHD1', 'polycystic kidney disease, autosomal recessive', 'polycystic kidney and hepatic disease 1']",0110861,,731,C0085548,"['0.476', '0.2788', '-0.4763', '0.09454', '0.2075', '-0.5166', '-0.5117', '1.017', '-0.617', '-0.01352', '-0.0979', '-0.6226', '0.4802', '0.181', '-0.6836', '-0.762', '-0.2588', '-0.03876', '0.1682', '-0.3813', '-0.3462', '-0.3423', '0.03812', '0.141', '-0.2308', '-0.3892', '-0.314', '0.667', '0.928', '-0.2072', '0.9766', '0.001739', '0.4614', '0.009476', '0.3032', '-0.663', '-0.618', '-0.02974', '0.5005', '-0.1611', '0.413', '0.4104', '0.3835', '0.2062', '-0.188', '0.08734', '-0.4766', '-0.1575', '0.2554', '0.4016', '-0.3274', '-0.0617', '0.9673', '-0.761', '0.2194', '-0.04684', '-0.3008', '0.5513', '-0.9214', '-0.0862', '0.2148', '0.302', '0.4668', '-0.2168', '0.2976', '0.05838', '0.0336', '0.392', '-0.27', '0.0815', '0.3716', '0.5', '0.1124', '-0.3306', '0.3035', '-0.004787', '0.3542', '0.2712', '-0.0527', '-0.167', '-0.2155', '0.2573', '0.162', '-0.266', '-0.05252', '0.155', '0.778', '-0.5366', '0.03001', '-0.1538', '-0.2957', '0.506', '-0.533', '0.1809', '0.603', '0.0009985', '0.1732', '-0.2834', '-0.1731', '-0.528']",C84579,,,753.14,,10036047,
mondo:0009890,Gillessen-Kaesbach-Nishimura syndrome,"['GIKANIS', 'Gillessen-Kaesbach-Nishimura syndrome', 'polycystic kidney disease, autosomal recessive, with microbrachycephaly, hypertelorism, and brachymelia', 'polycystic kidney disease, Potter type I, with microbrachycephaly, hypertelorism, and brachymelia']",,263210,,C1849762,,,,C564881,,,,
mondo:0009891,acquired polycythemia vera,"['polycythemia vera, somatic', 'Osler-Vaquez disease', 'polycythaemia rubra vera', 'proliferative polycythaemia', 'primary polycythemia', 'PRV', 'Osler-Vaquez syndrome', 'polycythemia vera', 'PV', 'acquired primary erythrocytosis', 'Vaquez disease', 'polycythemia rubra vera']",8997,263300,729,C0032463,"['-0.4036', '-0.3943', '-0.315', '-0.2178', '-0.0731', '0.4192', '-0.09344', '0.9326', '-0.3884', '-0.3748', '0.1186', '-0.0719', '0.0736', '0.01633', '-0.088', '-0.2966', '-1.002', '-0.1914', '0.4185', '-0.4246', '-0.5146', '-0.6562', '0.3735', '0.1769', '0.3079', '-0.1497', '-0.0762', '0.2798', '0.01275', '0.3274', '0.4636', '-0.2722', '0.4724', '0.1296', '-0.0422', '-0.10223', '-0.794', '-0.1755', '0.727', '-0.909', '0.4214', '0.3694', '0.2439', '-0.4158', '0.009766', '0.3884', '-0.637', '0.4436', '0.4421', '-0.2102', '0.2573', '0.6147', '0.3486', '-0.02173', '-0.1159', '0.1252', '0.3704', '0.010735', '-0.5654', '-0.4644', '-0.2952', '0.9595', '0.00348', '-0.7754', '-0.2812', '0.03958', '-0.09326', '0.1968', '-0.02135', '0.8296', '0.0214', '-0.0738', '-0.388', '-0.387', '0.568', '0.567', '0.10657', '-0.4563', '0.9116', '-0.0685', '-0.4937', '-0.3975', '0.6074', '-0.1283', '0.2244', '-0.2115', '0.4053', '0.3613', '0.3665', '-0.3125', '-0.012215', '-0.0536', '-0.3762', '-0.1842', '0.787', '0.4446', '0.10504', '-0.2827', '-0.3125', '0.1606']",C3336,0002429,D011087,238.4,D45,10036057,
mondo:0009892,Chuvash polycythemia,"['erythrocytosis, familial, 2', 'Chuvash erythrocytosis', 'VHL familial polycythemia', 'erythrocytosis, autosomal recessive benign', 'autosomal recessive benign erythrocytosis', 'familial erythrocytosis 2', 'familial polycythemia caused by mutation in VHL', 'erythrocytosis, familial, type 2', 'Chuvash type polycythemia', 'Von Hippel-Lindau-dependent polycythemia', 'polycythemia, VHL-dependent', 'ECYT2', 'polycythemia, Chuvash type', 'Chuvash polycythemia', 'Chuvash erythromatosis']",0060474,263400,238557,C1837915,"['-0.263', '0.00557', '-0.2394', '-0.279', '0.058', '0.3176', '-0.0004714', '0.2322', '-0.1324', '0.03775', '-0.142', '0.11725', '0.2354', '-0.0962', '-0.2822', '-0.1703', '-0.1735', '0.2234', '-0.1176', '-0.6064', '-0.09546', '-0.2278', '0.4421', '-0.08124', '0.3162', '-0.1814', '0.292', '-0.10364', '-0.1324', '-0.1037', '0.1544', '0.11426', '0.491', '0.1217', '-0.4138', '0.0722', '-0.05463', '-0.2163', '0.04172', '-0.4775', '0.03035', '-0.128', '0.1426', '-0.428', '-0.395', '-0.1494', '-0.1484', '0.0855', '0.1647', '0.04324', '0.1437', '0.0752', '0.10913', '-0.00947', '0.2231', '-0.0865', '0.2274', '-0.2355', '-0.4246', '0.07605', '0.0161', '0.1578', '0.0386', '-0.4666', '-0.1202', '-0.04465', '0.389', '0.4792', '-0.4583', '0.3118', '-0.1586', '0.2048', '-0.2153', '-0.3152', '0.3147', '-0.1107', '0.2068', '-0.02682', '0.04733', '-0.07684', '-0.1399', '-0.1512', '0.3464', '0.011765', '0.07043', '-0.0337', '-0.02295', '-0.01631', '0.2715', '-0.3257', '0.1812', '0.1754', '-0.1581', '-0.07654', '0.3362', '0.4182', '0.2603', '-0.1392', '-0.208', '0.006653']",,,C563918,,,,
mondo:0009893,"polydactyly, postaxial, type A5","['polydactyly, postaxial, type A5', 'PAPA5']",,263450,,C3550661,,,,,,,,
mondo:0009894,short-rib thoracic dysplasia 6 with or without polydactyly,"['polydactyly with neonatal chondrodystrophy, type II', 'Srps, type 2', 'short rib-polydactyly syndrome, type 2', 'short rib-polydactyly syndrome, type 2A', 'short rib-polydactyly syndrome type II', 'SRTD6', 'short rib-polydactyly syndrome type IIA', 'polydactyly with neonatal chondrodystrophy, type 2', 'Majewski syndrome', 'SRPS2A', 'polydactyly with neonatal chondrodystrophy type II', 'short-rib thoracic dysplasia 6 with or without polydactyly']",0110092,263520,,,,C122654,,,,,,
mondo:0009895,postaxial polydactyly-dental and vertebral anomalies syndrome,"['polydactyly, postaxial, with dental and vertebral anomalies']",,263540,2916,C1849732,,,,C564880,,,,
mondo:0009896,"polymyoclonus, infantile","['polymyoclonus, infantile']",,263550,,C1849731,,,,C535524,,,,
mondo:0009897,adult polyglucosan body disease,"['APBD', 'APBN', 'polyglucosan body neuropathy, adult form', 'polyglucosan body disease, adult', 'polyglucosan body disease, adult form']",,263570,206583,,"['0.1696', '-0.2397', '-0.0003667', '0.3047', '-0.5464', '-0.5747', '0.3318', '1.264', '-1.164', '-0.558', '0.2825', '-0.484', '0.1693', '0.4473', '0.657', '-0.0992', '-0.2712', '0.0733', '-0.401', '-0.5723', '0.51', '-0.0176', '-0.06525', '-0.1462', '0.02759', '-0.62', '-0.84', '0.507', '-0.402', '0.3638', '1.045', '-0.1594', '-0.3125', '-0.2627', '0.09235', '-0.563', '0.1455', '-0.185', '0.1455', '0.1127', '0.0707', '-0.586', '-0.0347', '0.6304', '-0.2025', '-0.454', '-0.3176', '-0.6353', '-0.0463', '0.5127', '-0.1505', '0.65', '-0.5513', '-1.103', '0.02094', '-0.2118', '0.365', '-0.8096', '-0.2284', '-0.444', '0.2532', '0.6846', '0.1165', '-0.2856', '-0.0595', '0.5425', '0.03763', '0.3938', '-0.2104', '-0.408', '-0.09454', '-0.101', '-0.3953', '0.03763', '0.4116', '0.27', '-0.01752', '0.409', '-0.3088', '-0.4062', '-0.09247', '-0.1688', '0.2603', '1.02', '0.00491', '1.183', '0.11633', '0.005207', '0.638', '-0.6', '0.3196', '-0.3235', '-0.4324', '-0.07874', '0.728', '0.3835', '0.541', '-0.2144', '0.05615', '0.299']",,,C564878,,,,
mondo:0009898,"polysaccharide, storage of unusual","['polysaccharide, storage of unusual']",,263600,,,,,,C564877,,,,
mondo:0009899,"polyhydramnios, chronic idiopathic","['Lactogen receptor defect of chorion', 'polyhydramnios, chronic idiopathic']",,263610,,C1849720,,,,C564876,,,,
mondo:0009900,polysyndactyly-cardiac malformation syndrome,"['Bonneau syndrome', 'polysyndactyly with CARDIAC malformation', 'polysyndactyly cardiac malformation']",,263630,2934,C1849719,,,,C564875,,,,
mondo:0009901,Bartsocas-Papas syndrome 1,"['popliteal pterygium syndrome, Bartsocas-Papas type 1', 'popliteal pterygium syndrome, Bartsocas-Papas type', 'popliteal pterygium syndrome lethal type', 'Bartsocas-Papas syndrome', 'autosomal recessive popliteal pterygium syndrome', 'Bartsocas Papas syndrome', 'lethal popliteal pterygium syndrome', 'pterygium, popliteal, lethal type', 'popliteal pterygium syndrome, lethal type', 'BPS', 'multiple pterygium syndrome, Aslan type', 'pterygium popliteal lethal type']",,263650,1234,C1849718,"['0.0686', '0.292', '0.08777', '-0.669', '0.3113', '-0.4824', '-0.366', '0.547', '-0.5605', '-0.575', '0.1263', '0.08826', '-0.3508', '-0.246', '-0.151', '0.323', '0.07886', '-0.5967', '-0.533', '-0.3538', '-0.3887', '0.1824', '0.3762', '0.2585', '0.1295', '0.0006146', '-0.3684', '0.502', '0.696', '-0.3108', '0.3086', '0.06995', '0.11346', '0.4321', '0.3037', '0.05002', '-0.196', '-0.2052', '0.038', '-0.2219', '0.05466', '-0.2172', '0.2485', '-0.1776', '0.0545', '-0.1465', '-0.12396', '0.6265', '0.2004', '-0.2166', '-0.2551', '-0.3376', '-0.2115', '0.007607', '-0.2913', '-0.533', '0.252', '0.01001', '0.0209', '0.14', '0.3743', '0.4944', '0.0924', '0.1705', '0.3555', '0.006203', '0.2922', '0.1672', '-0.32', '0.831', '-0.3994', '0.0098', '0.2125', '0.5938', '-0.1583', '-0.1232', '-0.3406', '-0.3286', '-0.295', '-0.327', '0.2164', '0.532', '-0.04102', '0.05594', '0.0588', '-0.03062', '-0.334', '0.2837', '0.3972', '0.05917', '0.2473', '0.596', '0.2715', '0.2032', '0.4873', '0.04318', '0.4531', '-0.643', '0.3525', '0.3315']",C168990,,C564874,,,,
mondo:0009902,cutaneous porphyria,"['Uros deficiency', 'congenital porphyria', 'uroporphyrinogen III synthase, deficiency of', 'uroporphyrinogen 3 synthase deficiency', 'Cep', 'congenital erythropoietic porphyria', 'Günther disease', 'erythropoietic porphyria', 'CEP', 'porphyria, congenital erythropoietic', 'Gunther disease']",13271,263700,79277,,"['0.05386', '-0.5015', '-0.8525', '-0.3223', '-0.2695', '-0.4385', '0.03105', '-0.136', '-0.5654', '0.0531', '-0.3213', '0.601', '-0.05548', '1.207', '-0.6294', '-0.0376', '0.359', '0.2732', '-0.311', '-0.689', '-0.1938', '-0.2395', '0.1929', '-0.4028', '0.1111', '-0.7065', '0.1044', '-0.0916', '0.3699', '-0.4758', '-0.2544', '-0.71', '0.655', '-0.7056', '-0.2903', '-0.3945', '-0.43', '-0.43', '0.1647', '-0.1842', '0.05', '-0.3372', '0.215', '-0.4197', '-0.1203', '-0.4817', '0.424', '-0.3818', '0.767', '0.1396', '-0.0906', '0.1729', '1.152', '0.2898', '-0.1266', '-0.02383', '-0.0717', '0.2188', '0.10846', '-0.876', '0.1835', '-0.2551', '0.7407', '0.1837', '-0.3953', '0.685', '-0.00403', '0.711', '0.433', '0.2637', '-0.488', '0.0735', '0.2047', '-0.6387', '0.2322', '0.5586', '0.1797', '-0.0801', '0.2242', '-0.2932', '0.1782', '-0.5615', '-0.252', '-0.4502', '0.5347', '0.4521', '1.009', '0.345', '-0.1499', '0.2537', '1.063', '-0.0733', '-0.3994', '0.3633', '0.3818', '1.133', '-0.2228', '-0.785', '0.3606', '0.2128']",C84697,,D017092,,,,
mondo:0009903,postaxial acrofacial dysostosis,"['Miller syndrome', 'acrofacial dysostosis, Genee-Wiedmann type', 'Genee-Wiedemann acrofacial dysostosis', 'POADS', 'Mandibulfacial dysostosis with postaxial limb anomalies', 'GWAFD', 'postaxial acrofacial dysostosis (POADS) syndrome', 'postaxial acrodysostosis', 'Wildervanck-Smith syndrome', 'Genee-Wiedemann syndrome', 'POADS syndrome', 'postaxial acrofacial dysostosis']",0111259,263750,246,C0265257,"['0.2603', '-0.03607', '0.2354', '-0.12256', '0.4744', '0.02177', '0.1807', '0.3926', '-0.569', '-1.182', '-0.015236', '-0.4058', '-0.5337', '0.1245', '0.00271', '0.1306', '0.6987', '-0.2905', '-0.4023', '-0.6353', '-0.347', '-0.3406', '-0.116', '-0.2534', '0.2603', '0.0713', '-0.339', '-0.1904', '0.7114', '-0.0715', '0.751', '-0.032', '-0.3345', '0.10504', '0.28', '-0.1768', '0.2397', '-0.4697', '-0.517', '-0.3423', '0.1984', '-0.3782', '0.1064', '-0.263', '0.1119', '-0.2603', '-0.0524', '0.647', '-0.2546', '0.001058', '-0.452', '-0.17', '0.0984', '0.09595', '-0.726', '-0.4192', '-0.1925', '-0.10815', '-0.3408', '-0.1398', '-0.3567', '0.0259', '-0.2966', '-0.2178', '-0.0175', '-0.4297', '0.3235', '0.9087', '0.1779', '0.1726', '-0.4094', '0.3394', '0.435', '-0.3184', '0.4473', '0.2091', '0.4724', '-0.806', '-0.3472', '0.01338', '0.3682', '-0.1581', '0.6226', '1.141', '0.04388', '0.1686', '-0.6074', '0.2277', '0.1538', '0.257', '0.1144', '0.5337', '0.1203', '0.281', '0.403', '-0.367', '0.52', '-0.9946', '0.06915', '0.2595']",,,C537680,759.89,,,
mondo:0009904,Gitelman syndrome,"['familial hypokalemia-hypomagnesemia', 'Gitelman^s syndrome', 'GTLMNS', 'hypomagnesemia-hypokalemia, primary renotubular, with hypocalciuria', 'primary renal tubular hypokalemic hypomagnesemia with hypocalciuria', 'Potassium and magnesium depletion', 'Gitelman syndrome']",0050450,263800,358,C0268450,"['0.375', '-0.4578', '-0.4568', '-0.2397', '-0.1009', '0.006203', '-0.3179', '1.447', '-0.03613', '0.1525', '-0.4285', '-0.3235', '0.0944', '0.715', '-0.2109', '0.0849', '0.05386', '0.02913', '-0.09015', '-0.781', '0.4165', '-0.5996', '0.3203', '0.4204', '0.1855', '-0.1654', '0.04898', '0.01962', '0.3994', '0.1035', '0.633', '-0.1771', '0.3389', '0.2627', '-0.583', '-0.1594', '0.02557', '-0.1906', '0.1079', '0.0568', '-0.1254', '-0.656', '0.86', '-0.605', '0.03473', '-0.3748', '-0.356', '0.286', '0.4287', '0.141', '-0.3684', '0.262', '0.2', '-0.3472', '0.0703', '-0.2039', '0.324', '-0.4468', '-0.276', '0.4114', '0.2306', '0.389', '-0.175', '-0.2896', '-0.3833', '0.1791', '-0.265', '0.129', '-0.3323', '0.474', '-0.316', '-0.09174', '0.05573', '0.3054', '0.369', '0.2234', '0.321', '-0.02736', '-0.5107', '-0.1494', '0.377', '-0.2394', '-0.03967', '0.1119', '0.0978', '0.5195', '0.2866', '-0.0699', '0.133', '-0.2432', '0.142', '-0.2075', '-0.4617', '-0.296', '0.1964', '0.1133', '0.2039', '-0.502', '-0.8735', '-0.0806']",C84730,,D053579,275.49,,10062906,
mondo:0009905,urban-Rogers-Meyer syndrome,"['Prader-Willi habitus, osteopenia, and camptodactyly', 'urban-Rogers-Meyer syndrome', 'intellectual disability-short stature-hand contractures-genital anomalies syndrome', 'Prader-Willi habitus-osteopenia-camptodactyly syndrome']",,264010,3409,C0796189,,,,C538276,,,,
mondo:0009906,prenatal bowing,['prenatal bowing'],,264050,,,,,,C564873,,,,
mondo:0009907,Prepapillary vascular loops,"['Prepapillary vascular loops', 'preretinal vascular loops']",,264060,,,,,,C563287,,,,
mondo:0009908,pterin-4 alpha-carbinolamine dehydratase 1 deficiency,"['hyperphenylalaninemia, Bh4-deficient, type D', 'CADH deficiency', 'hyperphenylalaninemia, tetrahydrobiopterin-deficient, due to pterin-4-Alpha-carbinolamine dehydratase deficiency', 'hyperphenylalaninemia due to pterin-4-alpha-carbinolamine dehydratase deficiency', 'PCBD1 deficiency', 'dehydratase deficiency', 'PCD deficiency', 'HPABH4D', 'hyperphenylalaninemia with primapterinuria', 'hyperphenylalaninemia, BH4-deficient, D', 'tetrahydrobiopterin (BH4)-deficient hyperphenylalaninemia (HPA) due to pterin-4-alpha-carbinolamine dehydratase deficiency', 'PCBD deficiency', 'pterin-4 alpha-carbinolamine dehydratase deficiency', 'hyperphenylalaninemia due to dehydratase deficiency']",0081131,264070,1578,,"['-0.647', '0.4497', '0.1561', '-0.4922', '-0.0287', '-0.2534', '-0.0786', '0.2651', '-0.0993', '0.04868', '-0.191', '-0.1993', '0.0922', '-0.2185', '0.3958', '0.2925', '0.1272', '-0.3933', '-0.3591', '-0.799', '-0.03038', '-0.1749', '0.08026', '-0.0889', '0.033', '-0.2603', '0.0968', '-0.1494', '-0.007755', '0.03986', '-0.05063', '0.3845', '0.2422', '0.0893', '-0.658', '0.01869', '0.4006', '-0.0837', '-0.1433', '-0.5093', '-0.06076', '-0.6646', '0.3728', '-0.3', '0.265', '-0.327', '-0.08154', '0.1627', '0.1854', '0.3992', '0.0799', '0.4043', '-0.03345', '-0.33', '0.149', '-0.4197', '0.2281', '-0.2446', '-0.5356', '0.5767', '-0.02353', '0.0833', '0.546', '-0.0815', '0.141', '0.05362', '0.1411', '-0.02205', '-0.2338', '0.1077', '-0.3108', '-0.2847', '-0.01517', '-0.565', '0.35', '0.2302', '0.2783', '-0.1697', '-0.557', '-0.1841', '0.3367', '-0.01347', '-0.0305', '0.0988', '0.411', '0.4963', '0.1299', '-0.1726', '0.5645', '0.2374', '0.02617', '0.2416', '-0.2244', '0.1445', '0.2776', '0.7793', '0.000771', '0.04666', '0.07605', '0.401']",,,C538382,277.6,,,
mondo:0009909,progesterone resistance,"['pseudocorpus luteum insufficiency', 'progesterone resistance']",,264080,,C1849699,,,,C564871,,,,
mondo:0009910,Wiedemann-Rautenstrauch syndrome,"['progeroid syndrome, neonatal', 'Wiedemann Rautenstrauch syndrome', 'neonatal progeroid syndrome', 'progeroid syndrome neonatal', 'Wiedemann-Rautenstrauch syndrome']",0081333,264090,3455,C0406586,"['-0.5605', '-0.04938', '-0.1074', '0.0829', '0.3374', '-0.489', '-0.2449', '1.024', '0.02571', '-0.1335', '-0.147', '0.11676', '0.383', '-0.294', '-0.2083', '0.03928', '0.8716', '-0.12006', '-0.2864', '-0.7305', '-0.3655', '-0.222', '0.4617', '-0.5063', '0.4453', '-0.2886', '-0.4026', '-0.4966', '0.279', '-0.225', '0.833', '-0.2937', '0.04376', '0.1098', '-0.1858', '0.5205', '-0.367', '-0.2598', '-0.07983', '0.0533', '0.07117', '-0.0836', '-0.2515', '0.26', '0.0896', '-0.4626', '0.1876', '0.2766', '-0.05844', '-0.5747', '0.05438', '-0.08386', '-0.0822', '0.4768', '-0.2593', '-0.2886', '0.145', '-0.3489', '0.1038', '-0.01805', '-0.03372', '0.0905', '-0.097', '-0.4272', '0.1532', '-0.011604', '0.04538', '0.455', '-0.4053', '0.28', '-0.2244', '0.5845', '0.556', '0.3503', '-0.2383', '0.1399', '0.0499', '-0.4023', '0.2197', '-0.2045', '0.12476', '-0.03336', '-0.2854', '0.2905', '0.3577', '0.1335', '-0.1058', '-0.07135', '0.469', '0.641', '0.0699', '0.721', '0.1027', '0.1737', '0.4292', '0.3438', '0.4673', '-0.4675', '0.4607', '0.093']",C121565,,C536423,259.8,,,
mondo:0009911,"prolactin deficiency, isolated","['prolactin deficiency, isolated']",,264110,,,,,,C562708,253.4,,,
mondo:0009912,prolactin deficiency with obesity and enlarged testes,"['prolactin deficiency with obesity and enlarged testes', 'PRL deficiency with obesity and enlarged testes']",,264120,,C1849698,,,,C564870,,,,
mondo:0009913,"prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness","['prune belly syndrome with pulmonic stenosis, intellectual disability, and deafness', 'prune belly syndrome with pulmonic stenosis, mental retardation, and deafness']",,264140,,C0403551,,,,C562894,,,,
mondo:0009914,pseudodiastrophic dysplasia,"['pseudodiastrophic dysplasia', 'Pseudodiastrophic dwarfism']",,264180,85174,C0432206,,,,C535826,756.9,,,
mondo:0009915,"46,XX disorder of sex development-skeletal anomalies syndrome","['female pseudohermaphroditism-skeletal anomalies syndrome', 'pseudohermaphroditism, female, with skeletal anomalies']",,264270,2975,C1849696,,,,C564869,,,,
mondo:0009916,"46,XY disorder of sex development due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency","['Male pseudohermaphroditism due to 17-beta-hydroxysteroid dehydrogenase 3 deficiency', '17-beta hydroxysteroid dehydrogenase 3 deficiency', '17 beta HSD3 deficiency', '17 alpha KSR deficiency', 'neutral 17 beta hydroxysteroid oxidoreductase deficiency', '17-BETA hydroxysteroid dehydrogenase III deficiency', 'Male pseudoherma-phroditism with gynecomastia', '17-ketosteroid reductase deficiency of testis', '17 beta hydroxysteroid dehydrogenase III deficiency', '17-ketoreductase deficiency', '17-KSR deficiency', '17-ketosteroidreductase deficiency', '17-beta-hydroxysteroid dehydrogenase 3 deficiency', '17 Beta HSD3 deficiency', '17-Beta hydroxysteroid dehydrogenase 3 deficiency', '17 alpha ketosteroid reductase deficiency of testis', 'pseudohermaphroditism, Male, with gynecomastia', 'neutral 17-Beta-hydroxysteroid oxidoreductase deficiency', 'polycystic ovarian disease due to 17-ketosteroid reductase deficiency', 'polycystic ovary syndrome due to 17-ketosteroid reductase deficiency']",0112248,264300,752,,"['-0.7256', '0.1112', '-0.223', '-0.10376', '0.5117', '-0.008606', '-0.373', '0.602', '-0.6494', '-0.5786', '0.0867', '0.1659', '-0.2198', '0.38', '-0.0536', '0.0977', '0.5073', '0.07336', '-0.2515', '-0.5786', '-0.6016', '-0.0825', '1.36', '-0.0751', '0.3442', '-0.1148', '0.02213', '0.4175', '0.06604', '-0.2328', '0.604', '0.1619', '0.5796', '-0.05963', '-0.3418', '-0.4412', '0.1573', '0.02122', '-0.01535', '-0.16', '0.581', '0.02702', '0.0568', '0.5825', '-0.1733', '-0.5044', '0.2632', '-0.2152', '0.2285', '0.7764', '0.1384', '-0.7075', '-0.3208', '-0.1694', '-0.2583', '0.1362', '0.881', '-0.1897', '-0.427', '0.1975', '0.253', '0.869', '0.2427', '0.4902', '0.0337', '0.537', '0.4097', '0.3623', '-0.2786', '-0.3037', '-0.1186', '0.0895', '-0.428', '-0.03041', '-0.2627', '-0.3418', '0.207', '0.09', '-0.8364', '-0.4722', '0.2012', '0.56', '0.2644', '-0.2717', '0.011986', '-0.3613', '-0.2944', '-0.2451', '0.487', '-0.5327', '-0.1251', '0.2434', '-0.2445', '-0.47', '1.083', '0.08795', '0.09296', '0.1821', '-0.07336', '-0.0955']",C120203,,C564868,,,,
mondo:0009917,autosomal recessive pseudohypoaldosteronism type 1,"['pseudohypoaldosteronism type 1, recessive', 'generalized PHA1', 'PHA I, autosomal recessive', 'autosomal recessive pseudohypoaldosteronism type 1', 'pseudohypoaldosteronism, type I, autosomal recessive', 'PHA1B', 'generalized pseudohypoaldosteronism type 1', 'generalised PHA1', 'pseudohypoaldosteronism type 1 autosomal recessive', 'autosomal recessive PHA 1', 'generalised pseudohypoaldosteronism type 1']",0060854,264350,171876,,"['0.02841', '0.01666', '-0.4456', '0.133', '-0.2085', '-0.01569', '0.1823', '0.505', '-0.154', '-0.001803', '-0.527', '-0.0654', '-0.667', '0.737', '-0.2966', '0.08374', '0.3103', '0.1931', '-0.2345', '-0.471', '0.2642', '-0.2339', '0.8555', '-0.3943', '0.4187', '-0.04886', '0.0852', '-0.01811', '-0.1749', '-0.3308', '0.503', '0.2788', '0.1621', '0.2935', '-0.1312', '-0.0776', '-0.09955', '0.2162', '-0.1514', '0.357', '0.185', '-0.5293', '0.511', '-0.2017', '0.11304', '0.3447', '-0.5073', '0.01034', '-0.2224', '0.4758', '-0.4795', '-0.0678', '0.907', '-0.2195', '-0.492', '0.10187', '0.4495', '-0.1527', '-0.03836', '0.0701', '0.1334', '0.01741', '-0.1622', '-0.509', '0.01819', '-0.0259', '0.4658', '0.2484', '-0.2761', '0.2722', '-0.5093', '-0.1432', '0.0597', '-0.082', '-0.2695', '-0.1914', '0.432', '0.05383', '0.131', '0.01512', '-0.0682', '0.5684', '-0.2317', '0.216', '-0.2231', '0.4663', '0.4343', '-0.1584', '0.1909', '-0.1327', '0.3323', '-0.08826', '-0.3088', '-0.1791', '0.537', '0.4229', '0.2668', '-0.662', '-0.2012', '0.5894']",,,,,,,
mondo:0009918,"fundus dystrophy, pseudoinflammatory, recessive form","['fundus dystrophy, pseudoinflammatory recessive form', 'PFD Lavia type', 'fundus dystrophy, pseudoinflammatory, recessive form', 'Pfd, Lavia type', 'pseudoinflammatory fundus dystrophy', 'Pfd, Finnish type']",,264420,,C1849694,,,,C535828,,,,
mondo:0009919,peroxisomal acyl-CoA oxidase deficiency,"['Pseudoadrenoleukodystrophy', 'ACOX1 deficiency', 'straight-chain acyl-Coa oxidase deficiency', 'peroxisomal acyl-CoA oxidase deficiency', 'peroxisomal acyl-coenzyme A oxidase', 'pseudo-NALD', 'pseudo-neonatal adrenoleukodystrophy', 'Pseudoneonatal adrenoleukodystrophy']",0050797,264470,2971,C1849678,"['0.173', '0.619', '-0.05936', '0.4385', '0.1744', '-0.2937', '0.3862', '0.3967', '-0.7188', '-0.4211', '0.2418', '-0.3323', '0.005768', '-0.09326', '-0.2996', '-0.4094', '0.2595', '0.0855', '-0.4927', '-0.303', '-0.04892', '-0.08093', '0.2214', '-0.03119', '-0.2345', '-0.2883', '-0.3545', '0.00265', '0.1323', '-0.2117', '0.6045', '0.1101', '0.254', '-0.02405', '-0.32', '-0.3713', '-0.324', '-0.1904', '-0.5537', '0.2283', '0.2203', '-0.1099', '-0.1598', '0.10126', '0.001948', '-0.2505', '0.2073', '0.1692', '-0.176', '0.272', '-0.0788', '-0.0374', '-0.5015', '0.2554', '0.365', '-0.932', '0.6143', '0.3008', '-0.0897', '0.761', '0.514', '-0.1609', '0.1884', '0.2883', '-0.02716', '-0.1371', '0.6284', '-0.08484', '-0.5244', '-0.1127', '0.2229', '0.3005', '0.09094', '-0.0722', '0.4717', '0.2289', '0.4739', '-0.581', '-0.5645', '-0.08167', '0.546', '-0.1511', '-0.0915', '0.2273', '0.3499', '0.5566', '-0.5044', '0.002928', '0.6333', '0.466', '0.5386', '0.5684', '-0.07996', '0.385', '0.2206', '0.363', '0.3706', '0.10626', '0.675', '0.04602']",C170437,,C536662,255.41,,,
mondo:0009920,Acrootoocular syndrome,"['acrootoocular syndrome', 'Aoo syndrome', 'pseudopapilledema-blepharophimosis-hand anomalies syndrome', 'pseudopapilledema, ocular hypotelorism, blepharophimosis, and hand anomalies']",,264475,2980,C1849661,,,,C564866,,,,
mondo:0009921,holoprosencephaly-postaxial polydactyly syndrome,"['pseudo trisomy 13 syndrome', 'pseudo-trisomy 13 syndrome', 'holoprosencephaly polydactyly syndrome', 'Young-Maders syndrome', 'PSEUDOTRISOMY 13 syndrome', 'holoprosencephaly-polydactyly syndrome']",,264480,2166,C1849649,,C125418,,C535829,,,,
mondo:0009922,Pseudouridinuria and mental defect,['Pseudouridinuria and mental defect'],,264500,,C1849648,,,,C564864,,,,
mondo:0009923,"46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency","['steroid 5-alpha-reductase deficiency', 'Male pseudohermaphroditism due to 5-alpha-reductase 2 deficiency', 'PPSH', '5 Alpha steroid reductase 2 deficiency', 'micropenis', 'Male pseudohermaphroditism due to 5-Alpha-reductase deficiency', '46,XY DSD due to 5-alpha-reductase 2 deficiency', '5-alpha reductase deficiency', '3-oxo-5 Alpha-steroid Delta 4-dehydrogenase deficiency', 'pseudovaginal perineoscrotal hypospadias', 'familial incomplete Male pseudohermaphroditism, type 2']",,264600,753,,"['-0.692', '-0.4744', '-0.3071', '-0.01509', '0.6543', '-0.2052', '-0.05618', '0.5586', '-0.656', '-0.2402', '-0.06903', '-0.02502', '-0.1018', '0.773', '0.01168', '-0.139', '-0.01604', '-0.0744', '-0.5503', '-0.6313', '-0.788', '-0.3208', '0.8413', '-0.3384', '0.2917', '-0.1461', '-0.2389', '0.5464', '0.1697', '-0.7305', '0.6606', '-0.0602', '-0.0775', '0.599', '-0.377', '0.2067', '0.1064', '-0.04303', '-0.1597', '-0.088', '0.738', '0.05664', '-0.3137', '0.09656', '-0.2866', '-0.4424', '-0.0668', '-0.403', '-0.2827', '0.2932', '0.1582', '-0.8105', '-0.3845', '0.1294', '-0.2185', '0.0929', '0.4565', '-0.261', '-0.52', '0.001913', '0.22', '0.474', '-0.2615', '0.624', '0.1405', '0.2417', '0.511', '-0.07605', '-0.2173', '0.2776', '-0.2927', '0.01192', '-0.11664', '0.09326', '0.6367', '-0.459', '-0.4294', '0.1084', '-0.8447', '-0.3723', '-0.3083', '0.6', '-0.1074', '-0.02324', '0.0545', '-0.12177', '-0.1752', '-0.02129', '0.4133', '-0.8906', '0.06247', '0.9463', '-0.2576', '-0.0551', '0.6045', '-0.702', '-0.2212', '-0.1624', '0.04828', '0.455']",C98699,,C535830,,,10000029,
mondo:0009924,"vitamin D-dependent rickets, type 1","['vitamin D 1 Alpha-Hydroxylase deficiency', '1 Alpha-hydroxylase deficiency', 'VDDR1', 'vitamin D dependent rickets type I', 'vitamin D-dependency type I', 'vitamin D-dependent rickets type 1', 'pseudo vitamin-D deficient rickets', 'PDDRI', 'VDDR-I', 'hypocalcemic vitamin D-dependent rickets', 'VDDI', '1-alpha-hydroxylase deficiency', 'vitamin D dependency, type 1', 'pseudovitamin D-deficient rickets', 'selective 1-alpha, 25-hydroxyvitamin D3 deficiency']",,,289157,,"['0.2935', '0.10724', '0.6006', '-0.0931', '-0.04858', '-0.007812', '-0.974', '1.537', '-0.1302', '0.02205', '0.562', '0.6646', '-0.769', '0.4458', '-0.557', '-0.02837', '0.0167', '0.1471', '-0.681', '-1.011', '0.06635', '-1.029', '0.5493', '-0.1486', '0.47', '-0.47', '0.1888', '-0.4932', '0.1667', '-0.02933', '0.1555', '-0.448', '-0.515', '-0.02068', '-0.1764', '-0.01395', '-0.2405', '0.0009174', '0.6035', '0.1178', '-0.4746', '-0.3318', '-0.4397', '0.0707', '0.02167', '-0.4116', '0.329', '-0.05942', '0.297', '0.3535', '-0.2607', '-0.656', '0.088', '0.06064', '-0.7324', '-0.47', '0.1696', '0.203', '-1.1', '0.1273', '0.726', '-0.2368', '-0.2896', '0.4607', '0.599', '0.777', '0.9272', '1.012', '-0.623', '-1.096', '0.541', '0.04803', '0.619', '-0.5576', '0.02878', '1.279', '0.36', '-0.8613', '0.3484', '0.4802', '0.354', '0.429', '0.523', '-0.05865', '-0.0447', '0.01203', '0.3093', '0.2607', '0.9727', '0.2673', '0.457', '-0.0422', '-0.565', '-0.0591', '-0.597', '0.331', '0.702', '-0.3596', '-0.6914', '-0.448']",C131073,,C562688,,,,
mondo:0009925,autosomal recessive inherited pseudoxanthoma elasticum,"['AR inherited pseudoxanthoma elasticum', 'Gronblad-Strandberg-Touraine syndrome', 'pseudoxanthoma elasticum', 'PXE', 'pseudoxanthoma elasticum, modifier of severity of', 'Gronblad-Strandberg syndrome', 'PXE, modifier of severity of', 'Gronblad Strandberg syndrome']",2738,264800,758,C0033847,"['0.113', '0.1181', '-0.4937', '-0.2544', '0.4143', '-0.3093', '0.293', '0.132', '-0.1484', '0.03128', '-0.5435', '-0.2296', '0.1298', '0.316', '0.02444', '0.1489', '0.07776', '-0.009895', '-0.376', '-0.1898', '-0.5327', '0.1289', '0.581', '-0.033', '-0.483', '0.03836', '-0.2266', '0.828', '0.2517', '-0.00826', '0.8057', '-0.2766', '0.2057', '0.01287', '-0.378', '0.2788', '0.04794', '-0.004513', '0.1462', '0.01149', '0.2128', '-0.5356', '0.257', '0.1675', '0.3733', '0.515', '-0.474', '-0.1063', '0.268', '0.1187', '0.09753', '0.0872', '0.538', '0.2117', '-0.127', '-0.10815', '0.848', '-0.4685', '-0.487', '-0.38', '-0.2462', '0.06384', '-0.4197', '0.295', '-0.1067', '0.3064', '0.3848', '0.761', '-0.3145', '0.567', '-0.4333', '0.0435', '0.03772', '0.2119', '0.253', '-0.2834', '0.1873', '0.4785', '-0.2123', '-0.346', '-0.401', '-0.635', '-0.2834', '-0.3054', '-0.1594', '-0.0862', '0.2527', '-0.2164', '0.3296', '-0.3083', '0.1965', '-0.1294', '-0.298', '0.2467', '0.7383', '-0.499', '0.1953', '-0.0951', '-0.1266', '-0.0757']",C85036,,D011561,757.39,,10037150,
mondo:0009926,autosomal recessive multiple pterygium syndrome,"['EVMPS', 'multiple pterygium syndrome nonlethal type', 'pterygium colli syndrome', 'pterygium syndrome', 'multiple pterygium syndrome, autosomal recessive', 'autosomal recessive multiple pterygium syndrome', 'multiple pterygium syndrome', 'multiple pterygium syndrome, ESCOBAR variant', 'multiple pterygium syndrome Escobar type', 'multiple pterygium syndrome, Nonlethal type', 'autosomal recessive non-lethal multiple pterygium syndrome', 'pterygium Universale', 'pterygium universale', 'Escobar syndrome', 'Escobar variant multiple pterygium syndrome']",,265000,2990,CN203342,"['-0.2703', '0.1588', '0.3447', '-0.5747', '0.083', '-0.535', '0.1168', '0.2903', '-0.6963', '-0.3694', '0.281', '0.06042', '-0.0857', '0.01289', '-0.1357', '0.2869', '0.14', '0.06335', '-0.0634', '-0.464', '-0.1322', '0.1703', '0.4304', '-0.2175', '0.08655', '0.2073', '-0.2969', '-0.0734', '0.3938', '-0.549', '0.0697', '-0.1398', '0.5703', '0.391', '0.2379', '-0.2546', '-0.2405', '-0.1945', '-0.1575', '-0.1045', '-0.04034', '-0.3354', '0.128', '0.05392', '0.11816', '-0.4792', '-0.02925', '0.441', '-0.011696', '0.135', '-0.437', '-0.038', '0.10925', '-0.196', '-0.3474', '-0.5625', '-0.2131', '0.09064', '-0.0218', '-0.1148', '0.5234', '-0.2461', '-0.2886', '0.3147', '-0.1423', '-0.04828', '0.3247', '0.06168', '-0.2445', '0.328', '-0.38', '-0.04626', '-0.06647', '0.03937', '-0.0681', '0.348', '-0.08844', '-0.1375', '-0.5034', '-0.0539', '0.0517', '0.11957', '0.0464', '0.6465', '-0.1646', '0.1577', '0.03848', '0.3115', '-0.02681', '0.01802', '-0.0835', '0.368', '0.66', '0.2073', '0.582', '0.06665', '0.857', '-0.3406', '0.4731', '0.221']",C101039,,,759.89,,,
mondo:0009927,3MC syndrome 2,"['Carnevale syndrome', 'Osa syndrome', '3MC2', 'ptosis of eyelids with diastasis recti and hip dysplasia', '3MC syndrome caused by mutation in COLEC11', '3MC syndrome type 2', '3MC syndrome 2', 'COLEC11 3MC syndrome', '3Mc syndrome type 2', 'oculo-skeletal-abdominal syndrome', 'Carnevale syndrome, formerly']",0060576,265050,2998,,"['-0.3896', '0.02885', '0.1649', '-0.1414', '-0.02168', '-0.354', '-0.06155', '0.2437', '-0.3513', '-0.0687', '0.03735', '-0.02682', '0.00518', '-0.02837', '0.02744', '-0.01396', '-0.0725', '-0.07404', '-0.09674', '-0.335', '0.331', '0.003565', '0.01341', '-0.02107', '0.1693', '-0.1396', '0.0773', '0.1295', '0.1661', '-0.0957', '0.09454', '0.0668', '0.4165', '0.2014', '0.11194', '-0.1786', '0.02205', '-0.08234', '-0.012405', '-0.2137', '0.1377', '-0.0953', '0.04565', '0.08386', '-0.1584', '-0.2605', '0.03384', '0.1449', '-0.0505', '-0.01729', '-0.2028', '-0.03952', '-0.0634', '0.00382', '-0.12396', '-0.218', '0.2458', '0.06238', '-0.1904', '0.1522', '0.089', '-0.006523', '0.1716', '0.03143', '-0.0462', '0.04178', '0.1124', '0.0797', '-0.2246', '0.08307', '-0.3047', '0.1798', '0.1283', '-0.1246', '0.07355', '-0.05383', '0.178', '-0.05118', '-0.2356', '0.0764', '0.0862', '-0.01822', '-0.0876', '0.1675', '-0.09454', '-0.1434', '0.1829', '0.3843', '0.1694', '0.1676', '0.05594', '0.0927', '0.222', '-0.07745', '0.5615', '0.066', '0.2534', '-0.3232', '0.149', '0.05017']",,1001977,C535586,,,,
mondo:0009928,pulmonary alveolar microlithiasis,['pulmonary alveolar microlithiasis'],12117,265100,60025,C0155912,"['-0.1208', '-0.1586', '-0.2898', '0.003952', '-0.1853', '-0.1552', '0.2113', '0.05273', '-0.602', '-0.2079', '0.1564', '0.262', '-0.1836', '0.0643', '-0.0923', '-0.1642', '0.1373', '0.0518', '-0.06537', '-0.552', '-0.1244', '-0.3193', '0.3337', '-0.308', '0.01668', '-0.279', '0.0756', '0.573', '-0.2333', '-0.1626', '0.2622', '-0.2922', '0.4932', '-0.10065', '0.2893', '-0.2281', '-0.03726', '0.318', '0.4077', '0.1494', '-0.02673', '-0.03375', '0.0885', '0.2598', '-0.154', '0.003637', '-0.6807', '0.324', '0.0729', '0.2053', '0.01153', '0.1611', '0.093', '0.10547', '0.08563', '-0.03683', '0.03482', '0.4353', '-0.2627', '-0.189', '0.2961', '0.2273', '-0.2281', '-0.349', '0.2354', '-0.543', '0.6235', '0.4714', '0.0442', '0.1532', '-0.2715', '-0.4644', '0.605', '0.1588', '0.1257', '0.1156', '-0.039', '0.361', '0.04712', '-0.281', '-0.1895', '-0.752', '0.2498', '0.08203', '-0.0356', '0.0706', '0.5117', '-0.1514', '0.2788', '0.3035', '0.1577', '-0.1864', '-0.3872', '0.3257', '0.615', '0.4353', '0.1622', '-0.3381', '-0.3865', '0.11066']",,,C562405,516.2,J84.02,10037315,
mondo:0009929,neonatal acute respiratory distress due to SP-B deficiency,"['surfactant metabolism dysfunction, pulmonary, type 1', 'interstitial lung disease, nonspecific, due to surfactant Protein B deficiency', 'pulmonary alveolar proteinosis, congenital, 1', 'pulmonary surfactant protein B, deficiency of', 'surfactant metabolism dysfunction, pulmonary, 1', 'SMDP1', 'interstitial lung disease due to surfactant Protein B deficiency', 'neonatal acute respiratory distress due to surfactant protein B deficiency']",,265120,217563,C1968602,"['-0.1625', '0.246', '-0.03494', '0.2114', '-0.02028', '-0.52', '0.05484', '-0.0609', '-0.1552', '0.04932', '-0.3042', '0.0395', '0.0483', '-0.145', '-0.1573', '-0.2479', '-0.0429', '0.1942', '0.00971', '-0.689', '-0.005127', '-0.5425', '0.684', '-0.2377', '0.0359', '-0.0975', '0.02386', '0.4272', '0.1332', '-0.1123', '0.2115', '0.4075', '0.1755', '-0.2168', '-0.0674', '-0.0211', '-0.1876', '-0.07196', '0.2172', '-0.02339', '-0.3223', '-0.3904', '0.3193', '0.3335', '-0.518', '0.10986', '-0.1857', '-0.05264', '0.2048', '0.1559', '-0.1759', '0.1274', '0.1475', '-0.02934', '-0.01901', '-0.3079', '-0.00987', '-0.0327', '-0.3472', '0.2175', '0.03735', '0.346', '-0.2059', '-0.1499', '0.2181', '-0.2659', '0.6206', '0.09155', '-0.2798', '0.1688', '-0.3296', '-0.1981', '0.234', '0.309', '-0.09814', '0.04736', '0.3298', '0.1142', '-0.211', '-0.0903', '-0.3557', '-0.1603', '-0.11597', '-0.0634', '-0.1893', '-0.02278', '0.3882', '0.504', '0.2693', '-0.05084', '0.273', '0.4216', '-0.2764', '-0.2284', '0.3164', '0.62', '0.36', '-0.5063', '-0.0197', '0.01121']",,,C566882,,,,
mondo:0009931,pulmonary atresia-intact ventricular septum syndrome,"['pulmonary valve atresia with intact ventricular septum', 'pulmonary atresia with intact ventricular septum']",,265150,1208,C0344975,,C99032,,C562832,,,,
mondo:0009932,pulmonary bullae causing pneumothorax,['pulmonary bullae causing pneumothorax'],,265200,,C1849566,,,,C564863,,,,
mondo:0009933,congenital pulmonary lymphangiectasia,"['pulmonary lymphangiomatosis', 'congenital pulmonary lymphangiectasis', 'pulmonary cystic lymphangiectasis', 'lymphangiomatosis pulmonary', 'lymphangiectasia pulmonary congenital', 'CPL', 'lymphangiomatosis, pulmonary', 'lymphangiectasia, pulmonary, congenital']",,265300,2414,C1849554,,C99034,,C537727,,,,
mondo:0009934,alveolar capillary dysplasia with misalignment of pulmonary veins,"['alveolar capillary dysplasia with misalignment of pulmonary vessels', 'foetal circulation', 'familial persistent pulmonary hypertension of the newborn', 'congenital alveolar capillary dysplasia', 'alveolar capillary dysplasia with misalignment of pulmonary veins and Other congenital anomalies', 'fetal circulation', 'alveolar capillary dysplasia with misalignment of pulmonary veins and other congenital anomalies', 'alveolar capillary dysplasia with misalignment of pulmonary veins', 'congenital alveolar capillary dysplasia with misalignment of pulmonary veins', 'persistent pulmonary hypertension of the newborn', 'ACDMPV', 'alveolar capillary dysplasia', 'persistent foetal circulation syndrome', 'persistent fetal circulation', 'alveolar capillary dysplasia with pulmonary venous misalignment', 'pulmonary hypertension, familial persistent of the newborn', 'persistent foetal circulation']",13042,265380,210122,C0031190,"['-0.4375', '0.02293', '0.0757', '-0.1149', '0.06525', '-0.3428', '0.3508', '0.1278', '-0.187', '0.02655', '-0.11847', '-0.203', '-0.02432', '-0.0628', '-0.3557', '-0.2822', '-0.3125', '0.2065', '-0.03937', '-0.6855', '0.02316', '0.1057', '0.6113', '-0.4812', '-0.1503', '-0.1251', '0.141', '0.3752', '0.4805', '-0.05338', '0.0821', '0.2', '0.729', '0.2397', '-0.0297', '-0.2666', '0.0575', '-0.0774', '0.1438', '-0.2998', '-0.1996', '-0.04773', '0.1907', '-0.0818', '-0.2595', '0.3137', '-0.2262', '0.3738', '0.05096', '0.1697', '-0.1227', '0.1672', '0.3103', '-0.02174', '-0.4065', '-0.07904', '-0.0972', '-0.2295', '-0.3157', '0.11444', '0.2542', '0.3967', '-0.005928', '-0.08295', '0.1181', '-0.4248', '0.6636', '0.2253', '-0.4604', '0.3142', '-0.365', '0.01193', '0.12463', '0.002535', '-0.4648', '-0.2369', '0.2003', '-0.3423', '-0.3777', '-0.06192', '-0.1855', '0.2355', '-0.10535', '0.2113', '-0.002972', '-0.10284', '0.4597', '0.274', '0.1432', '-0.2325', '0.2333', '0.1599', '-0.1354', '0.0237', '0.6167', '0.2744', '0.707', '-0.3396', '-0.03104', '0.2664']",C98809,1001103,C536590,747.83,,10054726,
mondo:0009935,"pulmonary hypertension, primary, autosomal recessive","['pulmonary hypertension, primary, autosomal recessive']",,265400,,C1849552,,,,C564862,,,,
mondo:0009936,familial primary pulmonary hypoplasia,"['primary pulmonary hypoplasia', 'pulmonary hypoplasia, primary', 'lung agenesis']",,265430,2257,CN226916,,,,,748.5,,,
mondo:0009937,pulmonary venoocclusive disease,"['obstructive disease of the pulmonary veins', 'PVOD', 'pulmonary veno-occlusive disease', 'pulmonary capillary hemangiomatosis']",5453,,31837,C0034091,"['-0.1827', '0.0782', '-0.0002046', '-0.1653', '-0.006763', '-0.1595', '0.1428', '0.1293', '-0.2186', '-0.05246', '-0.11945', '-0.09753', '0.002415', '0.003683', '-0.2233', '-0.2456', '0.01115', '-0.011375', '-0.008255', '-0.3308', '-0.02275', '-0.07074', '0.2269', '-0.1758', '-0.02731', '-0.02443', '0.0963', '0.202', '0.0699', '-0.0359', '0.1969', '0.0377', '0.2898', '0.1126', '0.0363', '-0.10425', '-0.01499', '-0.10443', '0.06244', '-0.2874', '0.04355', '-0.1114', '0.2145', '-0.0685', '-0.03024', '-0.04285', '-0.0842', '0.1635', '0.01581', '0.11707', '-0.0755', '0.064', '0.201', '0.05774', '-0.09216', '-0.02975', '0.095', '-0.0769', '-0.2634', '-0.00276', '0.0738', '0.104', '0.02568', '-0.07324', '0.04575', '-0.09906', '0.246', '0.16', '-0.2487', '0.265', '-0.2725', '-0.07697', '0.08246', '-0.047', '0.01075', '0.02393', '0.1199', '-0.06775', '-0.1052', '-0.1506', '-0.09064', '-0.01912', '0.052', '0.1569', '-0.00866', '-0.00528', '0.182', '0.2196', '0.1312', '-0.1606', '0.05853', '0.105', '-0.1309', '0.0939', '0.4634', '0.01436', '0.3174', '-0.2262', '-0.1142', '0.2037']",C85039,,D011668,416.8,,10037458,
mondo:0009938,pulmonic stenosis,"['valvular pulmonic stenosis', 'pulmonic stenosis', 'pulmonary stenosis', 'pulmonic stenosis (disease)']",,265500,,C1956257,,,,,,,,0001642
mondo:0009939,pulmonic stenosis and congenital nephrosis,['pulmonic stenosis and congenital nephrosis'],,265600,,C0403552,,,,C562895,,,,
mondo:0009940,pycnodysostosis,"['Pycd', 'PKND', 'Pyknodysostosis', 'pycnodysostosis']",0080038,265800,763,C0238402,"['0.1181', '0.0792', '0.01422', '-0.2303', '0.4', '0.2473', '0.005016', '0.968', '-0.754', '-0.2329', '-0.7197', '0.1924', '0.2725', '0.049', '-0.1967', '0.1718', '0.4338', '-0.8345', '-0.936', '-0.7754', '0.2266', '-0.2133', '0.6885', '0.05322', '0.2034', '0.0559', '0.2585', '0.00393', '0.7583', '-0.08154', '0.3303', '-0.2056', '-0.1477', '-0.02307', '0.1539', '0.02507', '0.1561', '-0.5015', '0.07825', '-0.3599', '-0.1356', '0.1699', '0.4722', '-0.11835', '0.3906', '-1.016', '-0.2444', '-0.1588', '0.635', '-0.4714', '0.2944', '-0.0257', '-0.3413', '0.1532', '-0.42', '-0.802', '0.05234', '-0.1444', '0.1567', '0.1335', '0.2164', '0.1941', '-0.3582', '-0.475', '0.1388', '0.4907', '0.3662', '0.01888', '-0.1248', '0.2773', '-0.3435', '-0.2942', '0.1445', '0.2034', '-0.07715', '-0.352', '0.3474', '0.02444', '0.2424', '-0.4182', '0.1225', '-0.362', '0.04272', '0.2411', '-0.0579', '0.5015', '0.03406', '-0.18', '0.8037', '0.0939', '-0.804', '0.2874', '-0.4368', '0.0462', '0.3794', '0.4084', '-0.2185', '-0.1278', '0.4082', '0.2659']",C131187,,D058631,,,,
mondo:0009941,Pygmy,"['Pygmy', 'Pygmy, African']",,265850,,C1849524,,,,,,,,
mondo:0009942,pyknoachondrogenesis,"['association of skeletal defects resembling achondrogenesis with generalized bone sclerosis', 'camera syndrome', 'association of skeletal defects resembling achondrogenesis with generalised bone sclerosis', 'pyknoachondrogenesis']",,265880,3003,C1849523,,,,C536251,,,,
mondo:0009943,Pyle disease,"['Pyle-Cohn syndrome', 'Pyle disease', 'metaphyseal dysplasia Pyle type', 'Pyle^s disease', 'chondrodysplasia calcificans metaphysealis', 'Bakwin-Krida syndrome', 'Pyle^s syndrome', 'metaphyseal dysplasia', 'Pyl', 'metaphyseal dysplasia, Pyle type']",0080019,265900,3005,,"['-0.62', '0.1185', '0.4165', '-0.4878', '0.2861', '-0.2366', '0.06976', '0.741', '-0.4502', '-0.2737', '-0.4292', '0.074', '-0.1976', '-0.1619', '-0.05084', '0.0706', '0.567', '0.0896', '-0.10736', '-0.564', '0.0753', '-0.1321', '0.571', '-0.51', '-0.07214', '-0.02652', '-0.0458', '0.0838', '-0.1378', '0.2007', '0.1982', '-0.4175', '-0.02953', '0.0342', '0.642', '-0.0686', '-0.2454', '-0.4102', '0.2524', '-0.5127', '0.307', '-0.504', '-0.1101', '-0.5215', '0.0648', '-0.2798', '-0.1242', '0.3862', '-0.01426', '-0.3574', '0.427', '-0.0969', '0.1023', '0.6187', '-0.5923', '-0.5303', '-0.1829', '0.03168', '-0.02159', '-0.0969', '0.3381', '0.03763', '-0.77', '-0.4988', '-0.3372', '-0.3823', '0.4717', '0.295', '-0.3296', '0.1224', '-0.07007', '0.05893', '0.3132', '-0.06506', '-0.2974', '0.464', '-0.248', '0.2417', '0.04648', '-0.5186', '-0.0936', '0.0671', '0.4504', '0.446', '-0.00804', '-0.2104', '-0.3264', '0.4', '0.066', '-0.05023', '0.05292', '0.4048', '-0.1467', '0.4653', '0.843', '0.2412', '0.751', '-0.859', '0.1582', '-0.2057']",,,C536252,758.5,Q78.5,,
mondo:0009944,pyloric atresia,['pyloric atresia'],,265950,,,,,,C562561,750.7,,,
mondo:0009945,pyridoxine-dependent epilepsy,"['Epd', 'pyridoxine-dependent epilepsy', 'antiquitin deficiency', 'pyridoxine dependency', 'EPD', 'pyridoxine dependency with seizures', 'epilepsy, pyridoxine-dependent', 'vitamin B6-dependent seizures', 'AASA dehydrogenase deficiency']",0080768,,3006,CN203406,"['0.959', '0.2463', '-0.4788', '-0.4155', '-0.5503', '-0.3516', '0.911', '0.5093', '-0.4766', '-0.4314', '-0.3362', '-0.311', '-0.001776', '0.3464', '-0.04483', '0.3215', '-0.5547', '-0.6763', '-0.3296', '-0.4402', '-0.0494', '0.2115', '0.1436', '-0.3313', '-0.2435', '-0.1436', '-0.12396', '-0.277', '-0.3687', '0.1464', '0.299', '-0.598', '0.08527', '0.4072', '0.493', '0.551', '0.0355', '0.05356', '-0.09235', '0.01614', '-0.1056', '-0.467', '0.1615', '-0.2123', '-0.327', '-0.693', '-0.1759', '0.1017', '0.1416', '0.816', '-0.1667', '-0.0945', '0.06604', '-0.4192', '0.09564', '-0.4136', '-0.411', '0.1726', '-0.2288', '0.3484', '-0.8774', '0.6436', '0.4563', '-0.4856', '-0.106', '1.071', '0.1074', '-0.0984', '-0.7153', '0.3992', '0.6084', '0.7295', '-0.04007', '-0.1388', '0.3845', '0.597', '0.885', '-0.02812', '-0.234', '0.2932', '-0.0841', '0.6904', '0.1792', '-0.128', '0.2534', '0.4011', '0.01581', '0.571', '0.611', '0.2019', '0.26', '0.3533', '-0.547', '-0.1099', '-0.04474', '0.1532', '0.2124', '-0.6123', '0.664', '0.3862']",,,C536254,,,,
mondo:0009946,hemolytic anemia due to pyrimidine 5^ nucleotidase deficiency,"['hemolytic Anaemia due to P5N deficiency', 'pyrimidine 5-prime Nucleotidase deficiency, hemolytic Anaemia due to', 'UMPH1 deficiency', 'uridine 5-prime monophosphate hydrolase deficiency, hemolytic anemia due to', 'P5N deficiency', 'uridine 5^-monophosphate hydrolase deficiency', 'pyrimidine 5-prime Nucleotidase deficiency, hemolytic Anemia due to', 'anemia, hemolytic, due to UMPH1 deficiency', 'uridine 5-prime monophosphate hydrolase deficiency, hemolytic anaemia due to', 'hemolytic Anaemia due to Umph1 deficiency', 'hemolytic Anemia due to P5N deficiency', 'hemolytic Anemia due to Umph1 deficiency', 'Umph1 deficiency']",,266120,35120,C1849507,"['-0.607', '0.4543', '-0.0461', '0.328', '0.5103', '0.0696', '-0.356', '0.6543', '-0.262', '-0.2615', '0.6724', '0.254', '0.332', '0.4292', '-1.151', '-0.01752', '-0.75', '0.1517', '-0.5293', '-0.49', '-0.1697', '-0.6206', '0.4841', '-0.4185', '0.578', '-0.3806', '-0.1818', '-0.3792', '0.54', '0.068', '0.1239', '0.074', '0.5005', '0.7964', '0.2297', '-0.42', '-0.8486', '-0.4504', '0.469', '-0.2998', '-0.6074', '0.267', '-0.03162', '-0.4773', '-0.8013', '-0.731', '0.35', '0.04907', '0.5073', '-0.1862', '0.337', '0.57', '0.6904', '-0.02332', '0.4055', '-0.6543', '-0.0167', '0.213', '-0.928', '0.1934', '-0.01493', '0.1835', '-0.2026', '-0.2795', '0.05853', '0.3164', '0.2764', '0.8994', '-0.638', '0.8066', '1.056', '-0.3376', '-0.577', '-0.5615', '0.4304', '1.05', '0.406', '0.1925', '0.163', '0.2239', '0.1599', '-0.001004', '-0.03354', '0.0877', '0.562', '-0.284', '-0.5713', '0.3074', '0.769', '-0.2474', '0.6367', '0.364', '-0.3625', '-0.0365', '0.5557', '1.031', '0.0846', '-0.042', '0.2969', '-0.5522']",,,C564859,,,,
mondo:0009947,glutathione synthetase deficiency with 5-oxoprolinuria,"['pyroglutamic aciduria', '5-oxoprolinuria', 'GSSD', 'glutathione synthetase deficiency']",0081034,266130,289846,,"['-0.7095', '0.2483', '-0.2935', '0.28', '0.12', '-0.11346', '-0.1366', '0.1431', '-0.10925', '-0.006367', '-0.291', '-0.0553', '0.08966', '0.117', '-0.1097', '-0.2178', '0.1157', '-0.02515', '-0.3352', '-0.4248', '0.10114', '-0.1703', '0.303', '-0.05246', '0.0594', '-0.2041', '0.0929', '0.014946', '-0.3252', '-0.00305', '0.04083', '0.2705', '0.1081', '0.3562', '-0.03366', '-0.2883', '0.0509', '0.01393', '-0.0912', '-0.2107', '-0.01694', '-0.258', '0.1332', '-0.0444', '-0.6553', '-0.284', '0.0963', '-0.01388', '0.0873', '0.2883', '-0.06903', '-0.3494', '0.1897', '0.03668', '-0.1094', '-0.01611', '0.6113', '-0.2715', '-0.3745', '0.3103', '0.1026', '0.3093', '0.2274', '-0.1344', '0.04846', '-0.0992', '0.2705', '0.02393', '-0.328', '-0.0487', '-0.0604', '0.08905', '-0.0434', '-0.1558', '0.1724', '0.05313', '0.08435', '0.0817', '-0.1086', '-0.0867', '-0.05896', '-0.1855', '0.1288', '0.0753', '0.2842', '0.1772', '-0.08484', '0.0735', '0.3652', '-0.10547', '0.2947', '0.1737', '-0.335', '-0.2583', '0.4539', '0.605', '0.0845', '-0.492', '-0.3298', '0.297']",,,,270.8,,,
mondo:0009948,"pyropoikilocytosis, hereditary","['HPP', 'pyropoikilocytosis hereditary', 'pyropoikilocytosis', 'pyropoikilocytosis, hereditary', 'hereditary pyropoikilocytosis']",,266140,98867,,"['-0.02599', '0.0369', '0.01082', '-0.00579', '-0.00249', '-0.065', '-0.00815', '0.0748', '-0.05673', '-0.007095', '0.00873', '0.01231', '-0.012375', '0.01701', '-0.00533', '-0.0158', '-0.00571', '-0.03806', '-0.00795', '-0.10986', '-0.005104', '-0.03763', '0.04898', '0.01978', '0.02492', '-0.01197', '0.00119', '-0.01129', '0.006855', '-0.04916', '0.01836', '-0.01541', '0.06137', '0.0374', '0.01555', '-0.03836', '-0.02504', '-0.02647', '-0.01532', '-0.06046', '0.01906', '-0.07623', '0.03967', '-0.01092', '-0.01012', '-0.05136', '-0.007317', '0.03244', '0.0219', '0.01814', '-0.00869', '-0.005356', '0.004387', '0.002537', '-0.02643', '-0.00839', '0.073', '-0.0166', '-0.0855', '-0.001591', '0.01639', '0.02763', '0.02908', '0.01703', '0.00135', '0.009', '0.0919', '0.0721', '-0.05594', '0.05417', '-0.03198', '0.02899', '0.03091', '-0.03995', '0.05768', '0.0508', '-0.002266', '0.01904', '-0.02283', '-0.01533', '-0.003092', '-0.00658', '-0.01566', '0.06113', '-0.01518', '-0.00858', '-0.001193', '0.05603', '0.0548', '-0.008156', '0.04742', '0.03017', '0.006355', '0.02332', '0.1159', '0.04022', '0.0519', '-0.0712', '-0.0235', '0.02676']",C98943,,C563004,790.09,,,
mondo:0009949,pyruvate carboxylase deficiency disease,"['Pc deficiency', 'Leigh syndrome due to pyruvate carboxylase deficiency', 'Leigh syndrome due to PC deficiency', 'deficiency of pyruvic carboxylase', 'Leigh necrotizing encephalopathy due to pyruvate carboxylase deficiency', 'pyruvate carboxylase deficiency', 'ataxia with lactic acidosis type 2', 'ataxia with lactic acidosis type II', 'ataxia with lactic acidosis 2']",3651,266150,3008,CN203409,"['-0.1986', '0.1854', '-0.2664', '0.1037', '0.2103', '-0.6353', '0.0971', '0.5483', '-0.3801', '0.04083', '-0.7075', '-0.2458', '0.4954', '0.3318', '0.1643', '0.7036', '-0.00887', '-0.1216', '-0.7886', '-0.671', '-0.09033', '-0.534', '1.047', '-0.2888', '0.1443', '-0.1599', '0.1311', '-0.3296', '-0.1', '-0.07367', '0.4631', '0.4531', '0.386', '0.223', '0.0641', '-0.27', '-0.2788', '-0.256', '-0.2423', '0.6807', '-0.4749', '-0.522', '0.04343', '0.3687', '0.2192', '-0.443', '-0.007626', '-0.04318', '-0.2167', '0.3699', '-0.1509', '-0.312', '0.05225', '-0.3323', '-0.2379', '-0.03232', '0.2317', '-0.1858', '-0.4917', '-0.02129', '-0.5083', '0.11127', '1.116', '-0.1445', '0.391', '0.2734', '0.304', '0.0162', '-0.4944', '0.2378', '-0.259', '-0.2876', '-0.387', '0.1655', '0.4888', '0.3396', '0.1941', '-0.3047', '-0.03497', '-0.0505', '0.524', '-0.1904', '-0.4226', '0.2369', '0.5137', '0.2646', '0.2383', '0.1033', '0.645', '-0.0605', '0.5527', '0.2441', '-0.11804', '0.1787', '0.5156', '0.9346', '0.1992', '-0.2295', '0.1433', '0.1312']",C85040,1001142,D015324,277.89,,,
mondo:0009950,pyruvate kinase deficiency of red cells,"['hemolytic Anemia due to pyruvate Kinase deficiency', 'hemolytic Anaemia due to pyruvate Kinase deficiency', 'hemolytic anaemia due to red cell pyruvate kinase deficiency', 'PK deficiency', 'pyruvate kinase deficiency of red cells', 'pyruvate kinase deficiency', 'pyruvate kinase deficiency of erythrocytes', 'pyruvate kinase deficiency of erythrocyte', 'Pk deficiency', 'hemolytic anemia due to red cell pyruvate kinase deficiency']",0111077,266200,766,C0340968,"['-0.9165', '-0.1881', '-0.793', '0.2272', '0.541', '-0.10474', '-0.471', '0.3806', '0.0894', '-0.2223', '0.2009', '-0.08636', '-0.10077', '0.00296', '-0.0907', '-0.1544', '-0.3943', '-0.921', '-0.531', '-0.8105', '-0.3142', '-0.1989', '0.8354', '0.1085', '0.4084', '-0.5195', '0.08075', '0.09546', '-0.1373', '-0.1923', '0.3293', '-0.2397', '0.306', '0.975', '-0.8267', '-0.3945', '-0.761', '-0.285', '0.1465', '-0.1549', '-0.2152', '0.09454', '0.4883', '-0.2505', '-0.2627', '-0.3972', '-0.1702', '-0.3215', '0.8354', '-0.235', '0.5576', '-0.653', '0.1976', '0.1445', '0.4812', '0.1032', '0.0603', '0.002556', '-0.437', '0.10376', '0.0173', '0.2715', '1.024', '-0.1672', '-0.0416', '0.07074', '0.334', '0.4077', '-0.3242', '0.8257', '0.183', '-0.4878', '-0.1519', '0.2479', '0.3003', '0.1952', '0.6167', '-0.298', '0.00755', '-0.152', '0.11993', '-0.504', '-0.3196', '0.004707', '0.08575', '0.3022', '0.0126', '0.4822', '0.6445', '-0.553', '0.5215', '0.351', '-0.4014', '-0.52', '0.525', '0.8633', '0.34', '-0.279', '0.7007', '-0.1606']",C99037,,C564858,,,,
mondo:0009951,"radiculoneuropathy, fatal neonatal","['Radiculoneuropathy, fatal neonatal']",,266250,,C1849471,,,,C564857,,,,
mondo:0009952,radioulnar synostosis-developmental delay-hypotonia syndrome,"['unilateral radio-ulnar synostosis, generalized hypotonia, developintellectual disability, and a characteristic facial appearance', 'Der Kaloustian-McIntosh-Silver syndrome', 'unilateral radio-ulnar synostosis, generalised hypotonia, developintellectual disability, and a characteristic facial appearance', 'unilateral radio-ulnar synostosis, generalised hypotonia, developmental retardation, and a characteristic facial appearance', 'unilateral radio-ulnar synostosis, generalized hypotonia, developmental retardation, and a characteristic facial appearance', 'radioulnar synostosis, unilateral, with developintellectual disability and hypotonia', 'radioulnar synostosis, unilateral, with developmental retardation and hypotonia']",,266255,3270,,,,,C564856,,,,
mondo:0009953,leukocyte adhesion deficiency type II,"['sialyl-Lewis X defect', 'CDGIIc', 'CDG syndrome type IIc', 'lad-type II', 'Rambam-Hasharon syndrome', 'SLC35C1-CDG', 'leukocyte adhesion deficiency, type II', 'congenital disorder of glycosylation, type IIc', 'leukocyte adhesion deficiency type 2', 'CDG IIc', 'CDG 2C', 'RHS', 'congenital disorder of glycosylation type IIC', 'LAD2', 'SLC35C1-CDG (CDG-IIc)', 'CDG2C', 'lad-II', 'CDG-IIc', 'leukocyte adhesion deficiency, type 2']",0080492,266265,99843,C0398739,"['-0.05673', '0.1174', '-0.0518', '-0.566', '-0.010414', '-0.3562', '0.507', '1.0205', '-0.05444', '0.2651', '-0.4553', '-0.0636', '0.261', '0.2837', '-0.4167', '-0.04126', '0.4915', '-0.02583', '-0.2969', '-0.6606', '-0.4194', '-0.11847', '0.4087', '0.2693', '0.191', '-0.2399', '-0.4482', '-0.3076', '-0.3208', '-0.2034', '-0.07446', '0.5903', '0.2152', '0.2247', '-0.4082', '0.1456', '-0.28', '-0.3245', '0.204', '-0.011185', '0.468', '-0.401', '-0.1908', '0.1', '0.1564', '0.191', '-0.06323', '-0.286', '-0.5737', '-0.4575', '0.01193', '-0.1947', '0.1958', '0.5503', '-0.2434', '-0.0315', '-0.3325', '-0.4072', '0.3044', '0.456', '-0.3757', '0.2822', '-0.0632', '0.135', '0.4607', '0.0713', '0.3372', '0.2238', '-0.1814', '0.3284', '-0.4717', '-0.4', '-0.02707', '-0.4204', '0.27', '0.1599', '0.3257', '0.0832', '0.0855', '0.4065', '0.4172', '-0.02438', '-0.7515', '0.516', '0.1979', '0.255', '0.0551', '0.341', '0.6733', '0.3354', '0.4263', '0.935', '0.428', '0.0541', '0.753', '1.055', '0.2306', '-0.706', '0.7275', '0.2173']",C4690,,C535755,,,,
mondo:0009954,Ramon syndrome,"['cherubism, gingival fibromatosis, epilepsy, mental deficiency, hypertrichosis, and stunted Growth', 'gingival fibromatosis combined with cherubism', 'cherubism-gingival fibromatosis-intellectual disability syndrome', 'Ramon syndrome']",,266270,3019,C0796133,,,,C535285,,,,
mondo:0009955,rapadilino syndrome,"['radial and patellar aplasia', 'rapadilino syndrome', 'absent thumbs, dislocated joints, long face with narrow palpebral fissures, long slender nose, arched palate', 'radial and patellar hypoplasia']",0050774,266280,3021,C1849453,"['-0.189', '-0.0541', '-0.3284', '-0.117', '0.325', '-0.4805', '-0.03958', '0.06415', '-0.7085', '-0.7715', '0.0932', '-0.3071', '0.269', '0.918', '0.0868', '0.4521', '0.589', '-0.01472', '-0.175', '-0.2322', '0.527', '-0.1111', '0.2607', '0.02747', '-0.1514', '0.1578', '-0.1442', '0.1503', '0.312', '-0.2947', '-0.04184', '-0.001596', '0.11945', '-0.1779', '0.3477', '0.3157', '-0.09265', '-0.1425', '-0.2737', '-0.05704', '-0.1166', '-0.128', '-0.04907', '-0.931', '0.1676', '-0.536', '0.34', '0.3857', '-0.3784', '-0.04984', '-0.497', '-0.439', '-0.1854', '-0.4033', '-0.5693', '-0.0672', '-0.03394', '-0.2076', '-0.3235', '0.2588', '0.4722', '-0.404', '-0.2241', '0.0778', '-0.306', '0.02632', '0.015114', '0.2576', '-0.3623', '0.709', '-0.875', '0.136', '-0.3257', '-0.3345', '0.3794', '0.1965', '-0.0756', '-0.593', '-0.1703', '-0.1833', '-0.1718', '-0.06616', '-0.1515', '0.3008', '-0.1672', '0.1732', '-0.08124', '0.2373', '-0.1559', '-0.2927', '-0.1964', '-0.2722', '-0.1929', '-0.1478', '0.544', '0.0863', '0.284', '-0.9775', '0.4932', '-0.1776']",,,C535288,759.89,,,
mondo:0009956,red skin pigment anomaly of new guinea,"['Red skin pigment, New Guinea type', 'red skin pigment anomaly of new guinea']",,266350,,C1849451,,,,C535515,,,,
mondo:0009957,Reese retinal dysplasia,['Reese retinal dysplasia'],,266400,,C1849450,,,,C564854,,,,
mondo:0009958,adult Refsum disease,"['Refsum disease with increased pipecolic acidemia', 'HMSN 4', 'hereditary sensory and motor neuropathy type 4', 'adult Refsum disease', 'RDPA', 'phytanic acid oxidase deficiency', 'HMSN type IV', 'phytanic-CoA hydroxylase deficiency', 'hereditary motor and sensory neuropathy 4', 'disorder of cornification 11 (phytanic acid type)', 'HSMN IV', 'Refsum^s disease', 'adult Refsum disease due to PHYH', 'hypertrophic neuropathy of Refsum', 'Refsum disease, adult, 1', 'DOC 11 (phytanic acid type)', 'Refsum disease', 'classic Refsum disease', 'Refsum disease, classic', 'heredopathia atactica polyneuritiformis', 'hereditary motor and sensory neuropathy type 4']",10582,600964,773,C1833022,"['-0.3403', '0.7983', '0.02086', '0.2479', '0.2069', '-0.2396', '-0.6772', '0.9775', '-0.3105', '-0.3372', '-0.01656', '-0.0943', '0.132', '-0.0975', '-0.03354', '-0.496', '-0.473', '-0.4058', '-0.4216', '-0.5483', '0.2532', '-0.431', '0.1814', '-0.1074', '-0.1313', '0.234', '-0.3545', '-0.1069', '0.5513', '-0.3296', '0.4587', '-0.4753', '0.02931', '0.2927', '0.1039', '-0.1447', '0.0522', '0.06146', '-0.4177', '0.1854', '-0.5303', '-0.2354', '0.3853', '0.3674', '0.568', '-0.3738', '0.1562', '0.6475', '-0.184', '0.7817', '-0.2974', '0.375', '0.307', '-0.9067', '0.351', '-0.377', '1.409', '0.2024', '-0.05945', '0.011765', '-0.1926', '-0.2856', '0.3882', '-0.431', '-0.4587', '-0.2175', '-0.1237', '0.5728', '0.0789', '-0.1146', '-0.09625', '0.04807', '-0.8394', '0.01974', '0.4517', '0.2505', '0.4937', '-0.314', '0.304', '-0.1907', '-0.2336', '-0.5415', '-0.452', '0.696', '-0.0347', '0.684', '-0.5264', '0.07935', '0.336', '0.638', '0.549', '0.179', '-0.2942', '0.04022', '0.2036', '-0.0803', '0.5693', '0.2018', '-0.1853', '-0.1915']",,,D012035,272.8,G60.1,10038275,
mondo:0009959,peroxisome biogenesis disorder type 3B,"['infantile phytanic acid storage disease', 'peroxisome biogenesis disorder type 3B', 'PBD3B', 'peroxisome biogenesis disorder 3B']",0081241,266510,,,,,,,,,,
mondo:0009960,inflammatory bowel disease 1,"['NOD2 inflammatory bowel disease', 'Crohn disease-associated Growth failure, susceptibility to', 'paediatric ulcerative colitis', 'inflammatory bowel disease (Crohn disease) 1', 'ulcerative colitis, paediatric', 'inflammatory bowel disease 1', 'ulcerative colitis, pediatric', 'ulcerative colitis', 'Crohn disease', 'IBD1', 'inflammatory bowel disease 1, Crohn disease', 'inflammatory bowel disease type 1', 'crohn disease-associated growth failure', 'pediatric ulcerative colitis', 'regional enteritis']",0110892,266600,,C0009324,,,,,555.9,,,
mondo:0009961,renal and mullerian duct hypoplasia,['renal and mullerian duct hypoplasia'],,266810,,C1849439,,,,C564853,,,,
mondo:0009962,Senior-Loken syndrome 1,"['Loken-Senior syndrome', 'NPHP1 Senior-Loken syndrome', 'Senior-Loken syndrome type 1', 'Senior-Loken syndrome caused by mutation in NPHP1', 'renal-retinal syndrome', 'renal dysplasia and retinal aplasia', 'SLSN1', 'juvenile nephronophthisis with Leber amaurosis', 'Senior-Loken syndrome', 'Senior-Loken syndrome 1', 'senior-loken syndrome-1', 'SENIOR-Loken syndrome 1']",,266900,,,,,,,759.89,,,
mondo:0009963,Ulbright-Hodes syndrome,"['renal dysplasia-mesomelia-radiohumeral fusion syndrome', 'Ulbright Hodes syndrome', 'RL syndrome', 'renal dysplasia-limb defects syndrome', 'renal dysplasia limb defects syndrome', 'renal dysplasia, mesomelia, and radiohumeral fusion']",,266910,3404,C1849438,,,,C537754,,,,
mondo:0009964,short-rib thoracic dysplasia 9 with or without polydactyly,"['renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia, and skeletal dysplasia', 'Mainzer-Saldino syndrome', 'SRTD9', 'Mainzer Saldino syndrome', 'Conorenal syndrome', 'renal dysplasia, retinal pigmentary dystrophy, cerebellar ataxia and skeletal dysplasia', 'Saldino-Mainzer syndrome', 'renal dysplasia-retinal pigmentary dystrophy-cerebellar ataxia-skeletal dysplasia syndrome', 'short-rib thoracic dysplasia 9 with or without polydactyly']",0110097,266920,140969,,"['-0.6694', '-0.272', '-0.03403', '-0.1874', '0.5044', '-0.6196', '-0.4053', '0.6714', '-0.3174', '-0.4268', '-0.1519', '-0.034', '-0.013176', '-0.276', '0.4163', '-0.05197', '0.4355', '-0.1218', '-0.3533', '-0.3691', '0.2822', '0.02219', '-0.1274', '-0.0715', '0.2025', '0.04196', '-0.11896', '-0.124', '0.257', '0.0387', '0.2766', '-0.1476', '0.1307', '-0.1677', '0.4229', '-0.1637', '0.0083', '-0.623', '-0.0947', '-0.167', '0.1091', '-0.4956', '0.04907', '-0.1277', '-0.2559', '-0.0688', '-0.0323', '0.3618', '0.1157', '-0.651', '0.1558', '0.1741', '-0.1092', '0.454', '-0.2153', '-0.6006', '0.522', '-0.1744', '-0.327', '0.07574', '0.443', '0.02379', '-0.05872', '0.1252', '-0.217', '-0.1613', '0.02249', '0.644', '-0.2012', '0.1805', '-0.485', '-0.1357', '0.06323', '-0.0982', '0.2354', '0.1447', '-0.01918', '0.12085', '-0.01926', '-0.04996', '0.1919', '0.262', '-0.0366', '0.3784', '-0.427', '-0.07465', '0.1305', '0.6226', '0.1433', '0.1654', '-0.2301', '0.02785', '-0.01675', '0.0499', '0.4844', '-0.00635', '0.508', '-0.414', '0.2161', '0.04843']",,,,759.89,,,
mondo:0009965,Perlman syndrome,"['nephroblastomatosis foetal ascites macrosomia and Wilms tumour', 'Perlman syndrome', 'renal hamartomas, nephroblastomatosis and foetal gigantism', 'nephroblastomatosis, fetal ascites, macrosomia and Wilms tumor', 'nephroblastomatosis - fetal ascites - macrosomia - Wilms tumor', 'nephroblastomatosis-fetal ascites-macrosomia-Wilms tumour syndrome', 'nephroblastomatosis, fetal ascites, macrosomia, and Wilms tumor', 'nephroblastomatosis, foetal ascites, macrosomia, and Wilms tumour', 'PRLMNS', 'nephroblastomatosis, foetal ascites, macrosomia and Wilms tumour', 'nephroblastomatosis - foetal ascites - macrosomia - Wilms tumour', 'renal hamartomas, nephroblastomatosis and fetal gigantism', 'nephroblastomatosis fetal ascites macrosomia and Wilms tumor', 'renal hamartomas, nephroblastomatosis, and foetal gigantism', 'nephroblastomatosis-fetal ascites-macrosomia-Wilms tumor syndrome', 'renal hamartomas, nephroblastomatosis, and fetal gigantism']",0060476,267000,2849,C0796113,"['-0.5', '0.0946', '-0.413', '-0.3013', '-0.2578', '-0.2532', '0.0596', '0.728', '-0.4326', '-0.4573', '0.365', '-0.578', '-0.005478', '-0.4915', '-0.4502', '-0.055', '0.0868', '-0.1718', '-0.2778', '-0.689', '0.6396', '0.08777', '0.2903', '0.218', '0.5015', '-0.10046', '-0.1167', '0.1665', '1.037', '-0.002695', '0.8706', '0.409', '-0.1559', '-0.476', '0.3577', '-0.07043', '-0.032', '-0.0877', '0.516', '-0.06274', '-0.4377', '-0.2559', '0.2805', '-0.1198', '0.0272', '-0.3276', '-0.2029', '0.05936', '-0.1282', '-0.4849', '-0.5312', '-0.1066', '-0.1022', '0.4595', '-0.561', '-0.3', '0.397', '-0.318', '-0.5093', '0.3755', '-0.03049', '0.03342', '0.0717', '-0.1995', '-0.1895', '0.01428', '0.0266', '0.1654', '-0.1819', '0.425', '-0.693', '0.224', '0.5723', '0.2366', '-0.544', '-0.1824', '0.61', '-0.2644', '-0.7754', '0.133', '-0.0732', '0.3118', '0.07263', '-0.0168', '0.0993', '-0.2153', '-0.1263', '0.1292', '0.1471', '0.378', '0.4836', '-0.4868', '0.7764', '0.2201', '1.022', '-0.1831', '0.4207', '-0.4106', '0.6416', '0.3845']",C103144,,C536399,,,,
mondo:0009966,NPHP3-related Meckel-like syndrome,"['renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome', 'MKS7', 'Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia', 'Goldston syndrome', 'Meckel-like syndrome type 1', 'NPHP3-related Meckel-like syndrome', 'renal-hepatic-pancreatic dysplasia with Dandy-Walker cyst', 'Meckel syndrome, type 7', 'Meckel syndrome 7', 'Meckel syndrome type 7', 'Meckel-Gruber syndrome, type 7']",0070121,267010,3032,C2673885,"['-0.06445', '-0.08966', '0.1024', '-0.1683', '0.094', '-0.03967', '-0.1465', '0.174', '-0.2455', '-0.0644', '-0.05417', '-0.3713', '-0.2416', '-0.1462', '-0.282', '-0.347', '0.0956', '-0.04437', '-0.1399', '-0.5913', '0.1549', '-0.05048', '0.3867', '-0.402', '-0.05078', '-0.1931', '-0.1516', '0.0643', '0.42', '-0.2988', '0.2964', '-0.003048', '0.529', '0.0356', '0.12384', '-0.1566', '-0.2402', '-0.1819', '-0.12177', '-0.1439', '0.08405', '-0.06665', '0.1564', '-0.1451', '-0.0656', '-0.3074', '-0.07025', '0.1348', '0.0407', '0.03772', '-0.03061', '0.1902', '0.1508', '-0.2769', '-0.4722', '-0.05667', '-0.01721', '-0.1423', '-0.604', '0.001437', '0.3413', '0.005867', '0.071', '0.0712', '-0.11945', '-0.2131', '0.3179', '0.2153', '-0.4814', '0.03885', '-0.3347', '0.12024', '0.2435', '0.157', '-0.02336', '-0.22', '0.351', '0.1123', '-0.3347', '-0.11755', '-0.2329', '0.2242', '0.0311', '0.3516', '-0.02554', '-0.2263', '0.434', '0.1873', '-0.1096', '-0.00548', '0.1567', '0.378', '0.09033', '-0.07324', '0.5303', '-0.006535', '0.571', '-0.4873', '0.2805', '0.376']",,,C537756,,,,
mondo:0009967,renal tubular acidosis 3,"['RTA, dislocation type', 'renal tubular acidosis, distal, type 3', 'renal tubular acidosis III', 'renal tubular acidosis 3', 'bicarbonate-wasting RTA', 'RTA, bicarbonate-wasting type']",,267200,,,,,,C537759,,,,
mondo:0009968,"renal tubular acidosis, distal, 2, with progressive sensorineural hearing loss","['renal tubular acidosis progressive nerve deafness', 'renal tubular acidosis, autosomal recessive, with progressive nerve deafness', 'autosomal recessive distal renal tubular acidosis with deafness', 'AR dRTA wth deafness', 'renal tubular acidosis type 1b', 'autosomal recessive distal renal tubular acidosis with hearing loss', 'renal tubular acidosis with progressive nerve deafness', 'distal renal tubular acidosis 2 with progressive sensorineural hearing loss', 'RTA with progressive nerve deafness', 'AR dRTA with hearing loss', 'renal tubular acidosis, distal, with progressive nerve deafness', 'renal tubular acidosis with deafness']",,267300,93611,C4302514,"['-0.0929', '0.08374', '0.0847', '0.01819', '-0.01634', '-0.09406', '0.01645', '0.262', '-0.0968', '-0.05212', '-0.1094', '-0.1395', '-0.0231', '0.0668', '-0.09784', '-0.09894', '0.0378', '-0.0538', '-0.05838', '-0.2893', '0.03754', '-0.0643', '0.06024', '0.0744', '0.1045', '-0.0758', '-0.0534', '0.02467', '-0.0258', '-0.03265', '0.0751', '0.01627', '0.1406', '0.0642', '0.01159', '-0.1274', '-0.0627', '-0.0705', '-0.05164', '-0.10254', '-0.03656', '-0.1611', '0.04483', '0.006977', '-0.02472', '-0.1606', '-0.11554', '0.0827', '-0.003883', '0.02023', '-0.0811', '0.02332', '0.0488', '-0.0791', '-0.03238', '-0.1215', '0.1404', '-0.0914', '-0.2251', '0.04837', '0.1149', '0.03107', '-0.01878', '0.01403', '-0.05978', '-0.04517', '0.1282', '0.2195', '-0.10236', '0.2028', '-0.10065', '-0.02864', '0.10187', '-0.10425', '0.0618', '0.02307', '0.0584', '0.0326', '-0.1031', '-0.04654', '-0.00777', '-0.007206', '0.06915', '0.1324', '-0.08905', '0.056', '0.03793', '0.0757', '0.1427', '-0.01755', '0.10583', '0.1334', '-0.03555', '0.02776', '0.2328', '0.03036', '0.1951', '-0.124', '-0.02663', '0.1098']",,,C562897,588.89,,,
mondo:0009969,renal-genital-middle ear anomalies,"['renal genital middle ear anomalies', 'renal, genital, and middle EAR anomalies']",,267400,1092,C1849432,,,,C564849,,,,
mondo:0009970,renal tubular dysgenesis of genetic origin,"['RTD', 'renal tubular dysgenesis with choanal atresia and athelia', 'genetic renal tubular dysgenesis', 'renal tubular dysgenesis', 'primitive renal tubule syndrome']",,267430,97369,,"['-0.09845', '-0.02574', '0.0848', '0.0359', '0.138', '-0.1305', '-0.1361', '0.2952', '-0.1355', '-0.2001', '-0.0615', '-0.2512', '0.0283', '-0.09576', '-0.2113', '-0.218', '0.1008', '-0.0625', '0.01793', '-0.706', '0.02545', '0.03168', '0.305', '-0.0958', '0.2642', '-0.0969', '0.1355', '0.1641', '0.03363', '0.002214', '0.2556', '0.1073', '0.2773', '-0.0697', '-0.10474', '-0.1323', '0.04514', '0.0641', '-0.1206', '-0.2064', '0.2151', '-0.08344', '0.1246', '-0.01895', '-0.0948', '-0.2268', '-0.09735', '-0.08966', '0.2312', '0.073', '-0.10406', '-0.1587', '-0.05713', '-0.03302', '-0.1295', '-0.4067', '0.0977', '0.09796', '-0.537', '0.1011', '0.3518', '0.03323', '0.231', '-0.06122', '-0.03625', '0.02039', '0.294', '0.258', '-0.3132', '0.1738', '-0.3364', '-0.04007', '0.2346', '0.04294', '-0.015144', '0.1047', '0.056', '0.05258', '-0.4128', '-0.06995', '-0.03284', '0.1768', '0.038', '0.09436', '-0.1444', '-0.1027', '0.2295', '0.01755', '0.1259', '-0.05743', '0.0899', '0.267', '-0.08514', '-0.05414', '0.2479', '-0.06207', '0.3887', '-0.2053', '-0.004208', '0.1598']",,,,,,,
mondo:0009971,respiratory distress syndrome in premature infants,"['respiratory distress syndrome, infant', 'respiratory distress syndrome in premature infants', 'hyaline Membrane disease', 'hyaline Membrane disease, formerly', 'RDS of prematurity', 'IRDS', 'infantile respiratory distress syndrome', 'respiratory distress syndrome', 'NRDS', 'RDS', 'RDS - infants']",,267450,70587,C1968593,"['-0.0245', '-0.1406', '-0.3318', '-0.09845', '-0.1102', '-0.01526', '0.418', '0.176', '-0.4827', '-0.1722', '-0.1051', '-0.04547', '0.09393', '0.388', '-0.3408', '0.099', '-0.2607', '0.1109', '-0.1343', '-0.6333', '-0.05948', '-0.10016', '0.5737', '-0.483', '0.0203', '-0.4949', '0.07025', '0.3684', '0.4563', '0.0714', '-0.0751', '0.04926', '0.439', '0.142', '-0.2498', '0.1537', '0.02325', '-0.002407', '0.1384', '0.1971', '-0.1991', '0.286', '0.2084', '0.0871', '0.02856', '-0.0736', '-0.3018', '0.4468', '-0.0317', '0.5806', '-0.2979', '0.04288', '0.1791', '-0.02895', '-0.08734', '-0.0759', '-0.1511', '0.155', '-0.04388', '-0.01967', '0.03207', '0.3838', '0.0757', '-0.0449', '0.1674', '-0.06696', '0.7217', '0.3333', '-0.4385', '0.5396', '-0.2854', '0.2468', '0.1671', '-0.10175', '-0.3186', '-0.03433', '0.2927', '-0.0634', '-0.3765', '-0.1088', '-0.3577', '0.129', '-0.09076', '-0.188', '-0.02206', '-0.004673', '0.3435', '0.2416', '0.388', '-0.487', '0.03406', '0.3691', '0.2551', '0.141', '0.0685', '0.2218', '0.3667', '-0.1562', '0.00449', '0.05176']",,1000644,C566881,,,,
mondo:0009972,respiratory underresponsiveness to hypoxia and hypercapnia,['respiratory underresponsiveness to hypoxia and hypercapnia'],,267480,,,,,,C564848,,,,
mondo:0009973,reticular dysgenesis,"['haematopoietic hypoplasia, generalised', 'reticular Dysgenesia', 'severe combined immunodeficiency with leukopenia', 'congenital Aleukia', 'congenital aleukocytosis', 'SCID with leukopenia', 'hematopoietic hypoplasia, generalized', 'DeVaal disease', 'reticular dysgenesis', 'De Vaal disease', 'RD', 'aleukocytosis', 'generalized hematopoietic hypoplasia', 'generalised haematopoietic hypoplasia', 'AK2 deficiency']",0060020,267500,33355,C0272167,"['-0.1265', '0.3884', '-0.3035', '-0.0655', '0.4448', '-0.381', '0.0362', '0.7163', '-0.1743', '-0.6133', '-0.1614', '-0.3354', '-0.6113', '-0.1863', '-0.5176', '0.09216', '0.3596', '-0.0508', '-0.2125', '-0.584', '0.10645', '-0.585', '1.226', '-0.613', '0.1959', '0.335', '-0.2507', '0.474', '0.06027', '-0.338', '0.1492', '0.5156', '0.3015', '-0.09534', '0.1603', '0.2251', '-0.6943', '-0.154', '-0.631', '0.1818', '-0.0885', '0.4688', '0.5186', '-0.45', '-0.311', '0.11993', '-0.3132', '-0.561', '-0.0845', '0.4973', '0.3655', '-0.486', '0.6484', '-0.282', '-0.2252', '-0.00962', '0.0736', '-0.7275', '-0.05847', '0.3948', '-0.0719', '0.1768', '0.106', '0.624', '0.0315', '-0.4553', '0.7363', '0.3472', '-0.2313', '0.8486', '-0.0734', '0.2264', '-0.5024', '-0.255', '0.2418', '-0.5063', '0.4485', '0.2423', '-0.1632', '-0.1906', '-0.5957', '-0.1953', '0.1259', '0.273', '0.02324', '0.2036', '0.1865', '-0.1542', '-0.1757', '-0.01773', '1.172', '0.2345', '0.2844', '0.1545', '0.437', '0.7363', '-0.1884', '-0.7637', '0.02055', '0.1688']",C27070,,C538361,,,,
mondo:0009974,familial hemophagocytic lymphohistiocytosis type 1,"['hemophagocytic lymphohistiocytosis, familial, 1', 'FHL1', 'HLH1', 'familial hemophagocytic lymphohistiocytosis type 1', 'Erythrophagocytic lymphohistiocytosis, familial', 'Hlh1', 'hemophagocytic reticulosis, familial', 'familial HLH', 'Hplh1', 'HPLH1', 'reticulosis, familial histiocytic', 'familial hemophagocytic lymphohistiocytosis 1', 'hemophagocytic lymphohistiocytosis, familial', 'familial hemophagocytic lymphohistiocytosis']",0110921,267700,,CN205265,,C61276,,,,,10070904,
mondo:0009975,reticulum cell sarcoma,"['reticular cell sarcoma', 'interdigitating cell sarcoma', 'histiocytic lymphoma', 'sarcoma of reticular cell', 'large-cell Lymphomas', 'Reticulum cell sarcoma', 'reticulosarcoma', 'reticulum cell sarcoma']",8538,267730,86900,,,C27824,0005287,D054739,200.7,,10038804,
mondo:0009976,retinal degeneration and epilepsy,['retinal degeneration and epilepsy'],,267740,,C1849416,,,,C564847,,,,
mondo:0009978,retinal degeneration-nanophthalmos-glaucoma syndrome,"['MacKay Shek Carr syndrome', 'Mackay-Shek-Carr syndrome', 'retinal degeneration with nanophthalmos, cystic macular degeneration, and angle closure glaucoma', 'retinal degeneration, nanophthalmos, glaucoma']",,267760,1574,C2931831,,,,C538364,,H35.5,,
mondo:0009979,reticular dystrophy of the retinal pigment epithelium,"['retinal dystrophy, reticular pigmentary, of POSTERIOR POLE', 'reticular dystrophy of retinal pigment epithelium']",,267800,99002,C1867332,"['-0.687', '0.06256', '-0.1752', '0.1105', '0.3882', '-0.4824', '-0.0715', '0.4658', '-0.6333', '-0.1348', '0.02513', '-0.1975', '-0.4612', '-0.2484', '-0.2457', '-0.3699', '0.3435', '-0.2632', '0.1957', '-0.741', '-0.3364', '-0.1469', '-0.078', '0.1764', '-0.10223', '0.2388', '-0.2361', '-0.02347', '-0.3079', '0.6045', '0.414', '-0.191', '0.1313', '0.4714', '0.01913', '0.5347', '-0.02078', '-0.1039', '-0.05215', '-0.5444', '0.518', '-0.3184', '0.3716', '0.1511', '-0.4893', '0.01761', '-0.285', '0.07513', '0.1283', '0.3608', '0.557', '0.02483', '0.1095', '-0.4531', '0.1362', '-0.294', '0.7085', '-0.05875', '-0.9355', '-0.351', '0.01386', '-0.228', '0.454', '0.12286', '-0.5312', '-0.4', '0.8394', '0.5923', '-0.096', '0.511', '-0.01785', '-0.007996', '0.4507', '-0.004623', '0.27', '-0.3428', '-0.2299', '0.02228', '-0.11334', '-0.3599', '0.231', '-0.1554', '-0.01318', '0.523', '-0.4453', '-0.2534', '-0.04083', '0.308', '0.1422', '0.2585', '0.2844', '0.7134', '0.3115', '0.506', '0.505', '-0.487', '0.1495', '-0.662', '-0.04346', '0.4165']",,,C566721,,H35.5,,
mondo:0009980,retinal telangiectasia and hypogammaglobulinemia,"['retinal telangiectasia associated with hypogammaglobulinemia', 'retinal telangiectasia and hypogammaglobulinemia', 'Frenkel Russe syndrome']",,267900,,C2930961,,,,C535638,,,,
mondo:0009982,retinitis pigmentosa inversa with deafness,['retinitis pigmentosa inversa with deafness'],,268010,,C1849405,,,,C564842,,,,
mondo:0009983,retinitis pigmentosa-intellectual disability-deafness-hypogenitalism syndrome,"['retinitis pigmentosa-intellectual disability-sensorineural hearing loss-hypogenitalism syndrome', 'retinitis pigmentosa, deafness, intellectual disability, and hypogonadism', 'retinitis pigmentosa-intellectual disability-deafness-hypogonadism syndrome', 'insulin-resistant diabetes with acanthosis nigricans, hypogonadism, pigmentary retinopathy, deafness, and mental retardation', 'retinitis pigmentosa-intellectual disability- labyrinthine deafness-hypogenitalism syndrome', 'retinitis pigmentosa, deafness, mental retardation, and hypogonadism', 'insulin-resistant diabetes with acanthosis nigricans, hypogonadism, pigmentary retinopathy, deafness, and intellectual disability']",,268020,3085,C1849401,,,,C564841,,,,
mondo:0009984,late-adult onset retinitis pigmentosa,"['retinitis pigmentosa, ^Senile^', 'retinitis pigmentosa, late-ADULT onset', 'senile retinitis pigmentosa']",0110421,268025,,C1849400,,,,C564840,,H35.5,,
mondo:0009985,retinohepatoendocrinologic syndrome,"['rhe syndrome', 'retinohepatoendocrinologic syndrome']",,268040,3087,C1849399,,,,C564839,,,,
mondo:0009986,"retinopathy, pigmentary, and intellectual disability","['retinal pigmentary degeneration, microcephaly, and severe mental retardation', 'retinopathy pigmentary mental retardation', 'retinopathy, pigmentary, and intellectual disability', 'retinopathy, pigmentary, and mental retardation', 'Mirhosseini-Holmes-Walton syndrome', 'retinopathy pigmentary intellectual disability', 'retinal pigmentary degeneration, microcephaly, and severe intellectual disability']",,268050,3084,,,,,C538367,,,,
mondo:0009987,autosomal recessive pericentral pigmentary retinopathy,"['retinopathy, pericentral pigmentary, autosomal recessive', 'retinitis pigmentosa, pericentral']",0110422,268060,,C1849398,,,,C564838,,H35.5,,
mondo:0009988,retinoschisis of fovea,"['retinoschisis of fovea', 'foveal retinoschisis', 'familial foveal retinoschisis']",,268080,,C1849397,,,,C538369,,,,
mondo:0009990,Revesz syndrome,"['retinopathy-anemia-central nervous system anomalies syndrome', 'DKCA5', 'Revesz-DeBuse syndrome', 'Revesz syndrome', 'exudative retinopathy with bone marrow failure', 'dyskeratosis congenita with bilateral exudative retinopathy', 'dyskeratosis congenita, autosomal dominant 5']",0070026,268130,3088,C1327916,"['-0.1311', '-0.04767', '0.1498', '-0.6123', '0.1826', '-0.6475', '0.02182', '0.585', '-0.2467', '-0.447', '-0.3796', '-0.4292', '-0.3464', '-0.581', '-0.1609', '-0.59', '0.1738', '-0.273', '0.1427', '-0.991', '-0.333', '-0.6104', '0.01008', '-0.0985', '0.1493', '0.5835', '-0.2433', '0.007526', '-0.262', '-0.8096', '0.00899', '0.2488', '0.3623', '0.5654', '0.1991', '0.585', '-0.4426', '-0.1927', '-0.428', '-0.708', '-0.1562', '-0.1715', '0.3652', '-0.696', '-0.07837', '0.02075', '-0.2003', '0.415', '0.1876', '-0.4211', '0.01007', '0.546', '0.2151', '0.12213', '-0.2444', '-0.604', '-0.04474', '-0.2568', '-0.5664', '-0.07355', '0.1226', '0.05472', '-0.1128', '-0.5815', '0.3499', '0.03403', '0.3691', '0.4316', '-0.4443', '0.718', '-0.08185', '0.01634', '-0.03017', '0.11066', '0.0335', '-0.3376', '-0.04526', '-0.5767', '0.05588', '-0.4065', '-0.1611', '0.1873', '-0.81', '0.471', '-0.0777', '-0.2081', '-0.167', '0.0777', '0.4531', '0.3374', '0.3489', '0.1554', '0.2025', '0.3257', '-0.05933', '-0.1163', '0.6963', '-0.0694', '0.1617', '-0.0359']",C152064,,C538371,,,,
mondo:0009992,"myoglobinuria, acute recurrent, autosomal recessive","['rhabdomyolysis, acute recurrent', 'myoglobinuria, familial paroxysmal paralytic', 'myoglobinuria, acute recurrent, autosomal recessive']",,268200,,C1849386,,,,C564832,,,,
mondo:0009993,embryonal rhabdomyosarcoma,"['spindle cell rhabdomyosarcomas (type of ERMS)', 'embryonal rhabdomyosarcoma (disease)', 'embryonal rhabdomyosarcoma', 'rhabdomyosarcoma chromosomal region', 'botryoid rhabdomyosarcoma (type of ERMS)', 'rhabdomyosarcoma 1', 'RMSE1', 'ERMS', 'rhabdomyosarcoma, embryonal, 1', 'rhabdomyosarcoma, somatic', 'rhabdomyosarcoma embryonal', 'rhabdomyosarcoma, embryonal, type 1']",3246,268210,99757,C0206656,"['-0.1247', '-0.0711', '0.5864', '0.3406', '-0.6543', '-0.4333', '0.115', '0.4746', '-0.683', '-0.02776', '0.2388', '0.10565', '0.1732', '0.7974', '-0.3987', '0.1681', '-0.2427', '-0.442', '-0.00589', '-0.7617', '0.001588', '-0.0685', '-0.0796', '-0.581', '0.2329', '-0.3467', '-0.3894', '0.4292', '-0.2532', '0.1567', '0.56', '-0.601', '0.4775', '-0.719', '0.1388', '0.03047', '-0.8096', '-0.305', '-0.2017', '-0.5176', '-0.278', '0.1233', '-0.1367', '-0.661', '0.6895', '0.221', '-0.1726', '-0.3752', '0.672', '0.00664', '-0.1895', '-0.1375', '0.3555', '-0.123', '-0.0696', '-0.3713', '-0.583', '0.5522', '-0.2515', '-0.2292', '-0.0385', '-0.2151', '-0.2146', '0.0955', '-0.397', '0.8926', '0.02885', '-0.4155', '-0.471', '1.312', '-0.00896', '0.385', '-0.323', '0.285', '0.299', '0.1247', '-0.5938', '0.1849', '0.11017', '-0.8076', '-0.257', '-0.1004', '-0.4216', '-0.04892', '-0.7246', '-0.507', '0.4897', '-0.07623', '0.3953', '0.02919', '-0.05923', '-0.01996', '-0.0875', '-0.0953', '0.6', '0.087', '0.08685', '-0.836', '-0.2502', '0.3784']",C8971,0000437,,171.9,,10065868,0006743
mondo:0009994,alveolar rhabdomyosarcoma,"['arms', 'alveolar rhabdomyosarcoma', 'alveolar rhabdomyosarcoma (disease)', 'rhabdomyosarcoma, alveolar', 'alveolar rhabdomyosarcoma (morphologic abnormality)', 'alveolar childhood rhabdomyosarcoma', 'rhabdomyosarcoma 2', 'rhabdomyosarcoma alveolar', 'pediatric alveolar rhabdomyosarcoma', 'monomorphous round cell rhabdomyosarcoma', 'rhabdomyosarcoma type 2', 'rhabdomyosarcoma, alveolar, somatic mutation', 'RMS2', 'paediatric alveolar rhabdomyosarcoma', 'rhabdomyosarcoma 2, alveolar, somatic mutation']",4051,268220,99756,C0206655,"['-0.1322', '0.06177', '0.4983', '0.2156', '-0.6167', '-0.4622', '0.2856', '0.4622', '-0.8457', '0.0716', '0.356', '0.1566', '0.28', '0.6978', '-0.519', '0.2834', '-0.2654', '-0.341', '-0.0188', '-0.7144', '-0.08057', '-0.05438', '-0.1729', '-0.652', '0.3447', '-0.356', '-0.394', '0.3872', '-0.4246', '0.2053', '0.5547', '-0.3965', '0.395', '-0.703', '0.1081', '0.10864', '-0.894', '-0.2269', '-0.152', '-0.516', '-0.2498', '0.10626', '-0.2192', '-0.733', '0.65', '0.2542', '-0.3296', '-0.2217', '0.704', '-0.011284', '-0.0999', '-0.1041', '0.452', '-0.1663', '-0.03033', '-0.2734', '-0.5815', '0.5767', '-0.4136', '-0.3267', '-0.03613', '-0.3652', '-0.1825', '-0.0725', '-0.4194', '0.786', '0.068', '-0.2534', '-0.409', '1.193', '-0.04684', '0.4495', '-0.29', '0.3625', '0.198', '0.12286', '-0.563', '0.452', '0.1704', '-0.987', '-0.2396', '-0.0972', '-0.3347', '-0.08234', '-0.819', '-0.4236', '0.4116', '0.0625', '0.2825', '0.1073', '-0.02875', '0.0636', '-0.11304', '-0.1779', '0.701', '0.0574', '0.2429', '-0.8193', '-0.144', '0.4038']",C3749,0000248,D018232,171.9,,10065867,0006779
mondo:0009996,"rhizomelic syndrome, Urbach type","['rhizomelic syndrome', 'rhizomelic dysplasia, familial', 'familial rhizomelic dysplasia']",,268250,3098,C1849382,,,,C537611,,,,
mondo:0009997,Roberts syndrome,"['Roberts-SC phocomelia syndrome', 'Roberts syndrome/SC phocomelia', 'Roberts tetraphocomelia syndrome', 'pseudothalidomide syndrome', 'SC phocomelia', 'SC phocomelia syndrome (mild variant of Roberts syndrome)', 'long bone deficiencies associated with cleft lip-palate', 'SC pseudothalidomide syndrome', 'tetraphocomelia-cleft palate syndrome', 'Appelt-Gerken-Lenz syndrome']",5325,,3103,,"['-0.2654', '-0.2832', '-0.1298', '-0.584', '0.5483', '-0.283', '0.3857', '0.66', '-0.615', '-0.8945', '-0.3813', '-0.5156', '0.2102', '0.6953', '-0.2421', '-0.1134', '0.4612', '-0.0538', '-0.304', '-0.3882', '0.368', '-0.02109', '0.4902', '-0.1376', '0.1418', '-0.289', '-0.4243', '-0.1796', '0.9414', '0.2129', '0.3772', '-0.387', '-0.1992', '0.2815', '0.141', '-0.1519', '-0.3823', '-0.2734', '-0.34', '-0.0912', '0.074', '-0.2026', '-0.05084', '-0.001087', '0.1189', '-0.3574', '-0.1231', '0.3777', '-0.413', '-0.01092', '-0.2703', '-0.2695', '-0.2141', '0.06604', '-0.8115', '0.06097', '-0.01116', '-0.559', '-0.1431', '0.3455', '-0.487', '-0.3137', '-0.1598', '0.4648', '0.0717', '-0.2898', '-0.2189', '0.3547', '-0.326', '0.1', '-0.2091', '0.2559', '0.4673', '0.2123', '0.002663', '0.2668', '0.1672', '-0.4946', '-0.3054', '-0.3677', '-0.1492', '-0.00409', '-0.034', '0.5127', '0.1539', '0.01671', '0.2024', '0.15', '0.0824', '0.133', '0.3813', '0.3293', '0.02739', '-0.0404', '0.6953', '0.03482', '0.4998', '-0.7935', '0.379', '0.3232']",C126326,,C535687,,,,
mondo:0009998,Richieri Costa-Pereira syndrome,"['short stature, Robin sequence, cleft mandible, pre/postaxial hand anomalies, and clubfoot', 'short stature-Pierre Robin syndrome-cleft mandible-hand anomalies clubfoot syndrome', 'ROBIN sequence with cleft mandible and limb anomalies', 'Richieri Costa Pereira syndrome', 'Richieri-Costa and Pereira form of acrofacial dysostosis', 'short stature-Pierre Robin sequence-cleft mandible-hand anomalies clubfoot syndrome', 'Richieri-Costa-Pereira syndrome']",,268305,3102,C1849348,"['-0.1261', '0.0946', '-0.0894', '0.06094', '0.425', '-0.574', '-0.349', '0.738', '-0.4531', '-0.7524', '0.1755', '-0.213', '0.326', '-0.1917', '0.0686', '0.2031', '0.3472', '-0.4739', '-0.2595', '-0.3738', '0.3604', '0.0995', '0.1941', '-0.1473', '0.4487', '0.1581', '-0.4246', '0.10156', '0.4604', '-0.5767', '0.392', '-0.2925', '0.04562', '-0.0008025', '0.0673', '-0.3586', '0.0963', '-0.151', '0.03818', '-0.616', '0.1578', '-0.03235', '-0.1903', '-0.4158', '-0.1376', '-0.2898', '0.2783', '0.2861', '-0.2744', '-0.3655', '-0.3713', '-0.2878', '-0.2866', '0.3228', '-0.2393', '-0.5703', '0.1525', '-0.0682', '-0.03937', '0.3787', '0.4075', '0.0941', '-0.2307', '-0.03424', '-0.371', '-0.116', '0.0565', '0.2369', '-0.4468', '0.4756', '-0.431', '0.1359', '0.1635', '0.1713', '0.0741', '0.4868', '-0.1024', '-0.2421', '-0.3594', '0.2546', '0.273', '0.2505', '0.3809', '0.6904', '-0.1024', '0.1926', '0.02875', '0.5957', '0.1571', '0.2446', '-0.3818', '0.3647', '0.1924', '-0.2712', '1.198', '0.04117', '-0.011055', '-0.6104', '0.1006', '-0.388']",,,C535677,,,,
mondo:0009999,autosomal recessive Robinow syndrome,"['costovertebral segmentation defect with mesomelia', 'Covesdem syndrome, formerly', 'Robinow syndrome, autosomal recessive', 'Robinow syndrome, autosomal recessive, with aplasia/hypoplasia of phalanges and metacarpals/metatarsals', 'Covesdem syndrome', 'costovertebral segmentation defect with mesomelia, formerly', 'costovertebral segmentation defect-mesomelia syndrome', 'COVESDEM syndrome', 'RRS', 'Robinow syndrome, autosomal recessive, with Brachy-syn-polydactyly']",0060764,268310,1507,C1849334,"['-0.2039', '0.3193', '-0.11066', '-0.806', '0.4749', '-0.4707', '0.01945', '0.6523', '-0.532', '-0.636', '-0.3313', '0.3274', '-0.243', '0.372', '-0.013565', '0.404', '0.4736', '-0.0182', '-0.1412', '-0.2974', '-0.632', '0.472', '0.61', '-0.4895', '-0.0712', '0.0693', '0.1074', '-0.4531', '0.6953', '-0.1746', '-0.2332', '-0.09406', '0.1266', '0.10516', '-0.0518', '-0.1501', '-0.1637', '-0.4153', '-0.298', '-0.02205', '0.02335', '-0.271', '0.002838', '0.0304', '-0.00667', '-0.2585', '-0.2412', '0.4714', '0.3813', '-0.1048', '0.411', '-0.1813', '-0.308', '-0.153', '-0.4902', '-0.5723', '0.2385', '-0.02757', '0.3208', '0.432', '0.2156', '-0.02887', '-0.3625', '0.1881', '-0.243', '0.05585', '0.3384', '0.3687', '-0.4336', '-0.0375', '-0.2761', '0.5234', '0.0824', '-0.1237', '-0.01107', '0.4888', '-0.1646', '-0.1783', '-0.5576', '-0.4048', '0.1991', '-0.02307', '0.1285', '0.282', '-0.0366', '0.523', '0.387', '0.3176', '0.0705', '0.3142', '0.00501', '0.7026', '0.1169', '0.08386', '0.9897', '0.2583', '0.7305', '-0.396', '-0.1423', '0.1678']",,,C535863,,,,
mondo:0010000,"rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction","['rod-cone dystrophy, sensorineural deafness, and Fanconi-type renal dysfunction']",,268315,,C1849333,,,,C564829,,,,
mondo:0010001,ectodermal dysplasia-blindness syndrome,"['microphthalmia, microcornea, and sclerocornea with short stature and hair and dental abnormalities', 'RODRIGUES blindness', 'microphthalmos, microcornea, and sclerocornea with short stature and hair and dental abnormalities']",,268320,1806,C1849332,,,,C535865,,,,
mondo:0010002,Rothmund-Thomson syndrome,"['poikiloderma atrophicans and cataract', 'poikiloderma of Rothmund-Thomson', 'RTS', 'poikiloderma congenitale', 'Rothmund-Thomson syndrome', 'congenital poikiloderma']",2732,,2909,C0032339,"['0.3496', '-0.00408', '0.4346', '-0.4148', '0.5356', '-0.5566', '0.06683', '0.6865', '-0.1328', '-0.651', '-0.1685', '0.38', '-0.2023', '-0.1401', '-0.4314', '0.3838', '0.8193', '-0.3196', '0.02786', '-0.5713', '-0.03723', '-0.2874', '0.2067', '-0.2428', '0.1188', '0.4998', '0.01399', '0.1182', '0.04504', '-0.5503', '0.3467', '0.006233', '0.07184', '0.151', '0.4226', '0.3215', '-0.809', '-0.6133', '-0.3313', '0.064', '-0.4614', '-0.1888', '0.4258', '-0.302', '0.3198', '0.2385', '0.0628', '0.0629', '0.2988', '-0.4639', '-0.0982', '-0.003544', '-0.2605', '-0.2076', '-0.3733', '-0.5312', '-0.1643', '0.052', '-0.799', '-0.4397', '0.1495', '-0.0368', '-0.4795', '-0.3198', '0.3306', '0.4495', '0.3782', '0.4968', '0.00618', '0.929', '-0.1156', '-0.2485', '0.1777', '-0.3706', '0.609', '-0.4136', '0.03418', '-0.4937', '0.329', '-0.2659', '0.3008', '0.2524', '-0.01663', '0.2043', '-0.759', '-0.4243', '0.4446', '0.1233', '0.6045', '-0.12317', '0.02295', '0.1223', '0.842', '-0.01726', '0.578', '0.4067', '0.683', '-0.1351', '0.3022', '-0.3845']",C3335,,D011038,759.89,,,
mondo:0010003,Rowley-Rosenberg syndrome,"['Growth retardation, pulmonary hypertension, and amino aciduria', 'Rowley-Rosenberg syndrome', 'Growth retardation, pulmonary hypertension, and aminoaciduria']",,268500,,C0268426,,,,C535874,,,,
mondo:0010004,EEC syndrome,"['Rudiger syndrome 1', 'ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome', 'RUDIGER syndrome', 'ectrodactyly-ectodermal dysplasia-cleft syndrome', 'ectrodactyly-ectodermal dysplasia-clefting syndrome', 'ectrodactyly-ectodermal dysplasia-cleft lip/cleft palate', 'Walker-Clodius syndrome', 'ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome', 'ectrodactyly-cleft lip/palate syndrome', 'ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome']",0060782,268650,1896,CN776907,"['-0.0502', '-0.0295', '0.4822', '-0.507', '0.466', '0.272', '-0.1578', '0.1595', '0.151', '-0.5596', '-0.2332', '-0.95', '-0.0115', '0.4204', '-0.1366', '0.4192', '0.3022', '-0.557', '-0.547', '-0.642', '-0.02203', '-0.3467', '0.327', '0.1797', '-0.3015', '-0.1476', '-0.7705', '0.4146', '0.4238', '-0.669', '0.4573', '-0.04996', '-0.05432', '0.06067', '0.4001', '-0.1835', '-0.526', '-0.0873', '-0.3074', '0.1506', '0.1954', '0.1367', '0.1836', '-0.0491', '0.664', '-0.407', '0.2744', '-0.2301', '-0.1732', '-0.4697', '-0.7007', '0.1234', '0.556', '0.3303', '-0.609', '0.04807', '0.02815', '-0.297', '-0.634', '-0.4993', '-0.1512', '-0.0336', '-0.009125', '0.1376', '-0.0364', '-0.03824', '0.1001', '0.385', '-0.1918', '0.3386', '-0.4087', '-0.2537', '0.01514', '-0.12366', '0.2251', '0.2805', '0.413', '-0.5376', '0.06604', '-0.1989', '0.3723', '-0.07745', '0.1564', '0.4062', '-0.501', '0.2335', '0.0657', '0.2185', '0.0908', '0.3008', '0.0496', '0.595', '0.0918', '0.4143', '0.782', '-0.539', '-0.02274', '-0.3943', '0.1154', '0.9375']",C148261,,C536189,,,,
mondo:0010005,saccharopinuria,"['saccharopinuria', 'Alpha-aminoadipic semialdehyde synthase deficiency', 'hyperlysinemia, type 2', 'hyperlysinemia type II', 'saccharopine dehydrogenase deficiency']",,268700,3124,C0268556,,,,C537218,270.7,,,
mondo:0010006,Sandhoff disease,"['GM2 gangliosidosis, 0 variant', 'Sandhoff disease, juvenile type', 'Sandhoff disease, infantile type', 'Beta-hexosaminidase-beta-subunit deficiency', 'hexosaminidase A and B deficiency disease', 'GM2-gangliosidosis, type 2', 'GM2 gangliosidosis 0 variant', 'Sandhoff disease', 'Hexosaminidases a and B deficiency', 'GM2 gangliosidosis, type 2', 'Hexosaminidases A and B deficiency', 'total hexosaminidase deficiency', 'Sandhoff Jatzkewitz disease', 'Sandhoff disease, infantile, juvenile, and adult forms', 'Sandhoff disease, adult type', 'Sandhoff-Jatzkewitz-Pilz disease']",3323,268800,796,C0036161,"['0.01657', '0.865', '-0.4766', '0.1204', '-0.12286', '-0.759', '-0.2386', '0.0624', '-0.258', '-0.05777', '-0.2876', '0.278', '0.01244', '0.505', '0.1687', '-0.2126', '0.03613', '-0.2303', '-0.3596', '-0.3684', '0.0678', '-0.502', '0.4895', '-0.08014', '-0.3657', '-0.2708', '0.00953', '0.05264', '-0.2252', '0.0916', '0.6733', '-0.02553', '0.09534', '-0.2439', '0.05576', '0.393', '-0.0886', '0.2355', '-0.6006', '0.327', '0.03128', '-0.326', '-0.1035', '0.1262', '-0.0674', '-0.1565', '0.129', '-0.4666', '-0.2234', '0.278', '-0.2463', '0.2247', '-0.1982', '-0.2532', '0.2233', '-0.1863', '0.3381', '-0.5044', '-0.239', '0.4265', '-0.216', '-0.0877', '0.2196', '0.322', '0.10706', '0.12085', '0.5654', '-0.255', '-0.3718', '0.00213', '-0.4087', '-0.6562', '-0.133', '0.2866', '0.11816', '0.10284', '0.3572', '0.4575', '-0.3027', '0.1559', '0.1713', '-0.5234', '-0.2109', '0.4607', '0.05054', '-0.1378', '0.2141', '0.005783', '0.7266', '0.1724', '0.2356', '0.4722', '-0.1295', '0.1588', '0.3936', '0.4756', '-0.1058', '-0.486', '0.382', '0.04474']",C85052,,D012497,,E75.01,,
mondo:0010007,microbrachycephaly-ptosis-cleft lip syndrome,"['short stature, intellectual disability, eye anomalies, and cleft Lip/palate', 'Richieri-COSTA/Guion-Almeida syndrome', 'microbrachycephaly ptosis cleft lip', 'short stature, mental retardation, eye anomalies, and cleft Lip/palate', 'Richieri Costa-Guion Almeida-Ramos syndrome', 'sao Paulo MCA/Mr syndrome']",,268850,2511,C0796142,,,,,,,,
mondo:0010008,sarcosinemia,"['hypersarcosinemia', 'sarcosinemia', 'SARD deficiency', 'SARCOS', 'sarcosine dehydrogenase complex deficiency', 'SARDH deficiency']",0112307,268900,3129,C0268563,"['-0.5083', '0.3586', '-0.1802', '-0.2043', '0.1605', '-0.2089', '-0.3655', '0.2786', '-0.0696', '0.08014', '-0.0579', '0.04712', '0.1241', '-0.1603', '0.00536', '0.10736', '0.06107', '0.225', '-0.2166', '-0.821', '-0.168', '-0.3616', '0.629', '0.0745', '-0.01101', '0.1212', '0.3147', '-0.06604', '-0.05505', '-0.1538', '0.247', '0.1176', '0.2805', '0.2306', '-0.528', '-0.1746', '0.03467', '-0.1779', '-0.00957', '-0.4285', '0.1294', '-0.6045', '0.3801', '-0.325', '-0.2106', '-0.514', '0.219', '-0.05032', '0.1803', '0.3413', '0.0666', '-0.1809', '-0.04544', '-0.4', '-0.164', '-0.1719', '0.3147', '-0.1573', '-0.2668', '0.10156', '0.2957', '-0.0464', '0.3093', '-0.285', '0.1421', '0.2208', '0.3086', '-0.01996', '-0.5474', '0.1646', '-0.2573', '-0.11743', '-0.2664', '-0.0722', '0.318', '0.1924', '0.2198', '0.131', '0.05807', '-0.0846', '0.1519', '0.1858', '0.0529', '0.0713', '0.1621', '0.2152', '0.02905', '-0.1342', '0.3552', '0.1741', '0.3125', '0.1802', '-0.4282', '-0.3054', '0.519', '0.431', '0.1602', '-0.4749', '-0.2484', '0.1207']",,,C537236,270.8,,10059299,
mondo:0010010,Schinzel-Giedion syndrome,"['Schinzel Giedion midface-retraction syndrome', 'Schinzel Giedion syndrome', 'Schinzel-Giedion midface retraction syndrome', 'Sgs', 'SGS', 'Schinzel-Giedion syndrome', 'Schinzel-Giedion midface-retraction syndrome']",,269150,798,C0265227,"['0.425', '-0.1971', '0.609', '-0.6904', '0.544', '-0.61', '0.3018', '1.06', '-0.4954', '-0.5464', '-0.127', '-0.3955', '-0.2815', '0.01163', '-0.3772', '0.2607', '0.0867', '-0.3428', '-0.1493', '-0.385', '0.0376', '0.822', '0.617', '-0.445', '-0.009674', '-0.7275', '-0.4253', '-0.1946', '0.726', '-0.03513', '0.2361', '-0.595', '-0.1115', '0.05978', '-0.05792', '-0.1104', '-0.0877', '-0.05887', '-0.3572', '-0.167', '-0.502', '-0.1786', '-0.03114', '-0.0981', '0.315', '0.0715', '-0.6484', '0.3555', '-0.9766', '0.3105', '-0.2303', '0.3054', '0.0159', '-0.3809', '-0.357', '0.1055', '0.1409', '-0.347', '0.09155', '0.0333', '-0.02434', '0.1382', '-0.4421', '0.1925', '0.07245', '-0.3035', '0.3826', '0.2947', '-0.718', '0.5605', '0.0895', '-0.009094', '-0.2124', '0.1489', '-0.4907', '-0.5522', '0.3972', '-0.4543', '-0.6323', '-0.2664', '0.1691', '0.2751', '0.459', '0.508', '0.0653', '0.1208', '0.1268', '0.5034', '0.4165', '-0.2303', '0.228', '0.3452', '0.232', '0.278', '0.8833', '0.602', '0.5415', '-0.3364', '0.1959', '0.1703']",C129308,,C536632,759.89,,10063540,
mondo:0010011,schizencephaly,['schizencephaly'],,269160,799,,"['-0.1396', '-0.0985', '0.4473', '-0.572', '0.07166', '0.03943', '0.252', '0.2367', '-0.737', '-0.426', '-0.831', '-0.602', '0.6465', '0.288', '0.554', '-0.2416', '-0.241', '-0.714', '-0.3499', '-0.903', '0.273', '0.2246', '0.9263', '-0.4707', '-0.3103', '-0.6694', '-0.399', '0.2196', '-0.0983', '0.1124', '0.2177', '-0.0898', '0.613', '-0.05328', '-0.0748', '0.0589', '-0.1462', '-0.2195', '-0.09973', '-0.3718', '0.6626', '0.2583', '-0.1886', '-0.4194', '0.01298', '-0.11847', '0.219', '-0.187', '0.0526', '0.389', '0.2085', '-0.0593', '-0.01659', '-0.208', '0.08026', '0.3489', '0.189', '-0.3042', '-0.349', '0.4539', '-0.2148', '-0.4578', '0.1241', '-0.03644', '-0.585', '0.6016', '0.512', '0.261', '-0.3206', '-0.2458', '0.01929', '0.4607', '0.235', '-0.3684', '-0.05984', '0.4697', '0.4673', '-0.2568', '-0.2329', '-0.49', '-0.4084', '-0.1498', '-0.3572', '0.718', '0.02403', '-0.4558', '-0.1797', '0.4924', '-0.0374', '0.1713', '0.1954', '0.3103', '-0.3965', '0.3281', '0.0827', '-0.634', '0.3657', '-0.2659', '0.7573', '0.10394']",C99056,,D065707,742.4,,,
mondo:0010012,autoimmune polyendocrinopathy type 2,"['autoimmune polyendocrine syndrome type 2', 'multiple endocrine deficiency syndrome, type 2', 'autoimmune polyendocrine syndrome, type II', 'APS type 2', 'polyglandular deficiency syndrome type 2', 'PGA 2', 'polyglandular autoimmune syndrome, type 2', 'autoimmune polyglandular syndrome type 2', 'autoimmune thyroid disease and/or type 1 diabetes-Addison disease syndrome', 'APS 2', 'Schmidt syndrome', 'Schmidt^s syndrome', 'diabetes mellitus, Addison disease, myxedema', 'polyendocrine autoimmune syndrome, type 2', 'APS2', 'diabetes mellitus, Addison^s disease, myxedema']",0050168,269200,3143,,,C129728,,,258.8,,,
mondo:0010013,schneckenbecken dysplasia,"['SLC35D1-CDG', 'schneckenbecken dysplasia', 'chondrodysplasia with snail-like pelvis', 'SHNKND', 'chondrodysplasia, lethal neonatal, with snail-like pelvis', 'chondrodysplasia lethal neonatal with snail like pelvis']",0050775,269250,3144,C0432194,"['-0.579', '0.1755', '0.1848', '-0.192', '0.362', '-0.2576', '-0.2517', '0.8125', '-0.2744', '-0.248', '-0.3325', '-0.07135', '-0.154', '0.0866', '-0.1062', '0.276', '0.3403', '0.0491', '-0.2166', '-0.3865', '0.00522', '0.1497', '0.451', '-0.282', '0.2598', '0.02245', '-0.1838', '-0.008286', '0.428', '-0.146', '0.1644', '-0.4712', '0.252', '0.3157', '0.513', '-0.2089', '-0.1903', '-0.4502', '0.12195', '-0.25', '0.0854', '-0.4517', '-0.1509', '-0.3877', '-0.02345', '-0.2566', '-0.2576', '0.585', '-0.2734', '-0.3313', '0.2174', '-0.1315', '-0.1736', '0.5083', '-0.54', '-0.516', '-0.0581', '-0.3264', '0.0771', '0.0781', '0.614', '0.2458', '-0.3389', '-0.01678', '-0.01151', '-0.1842', '0.2234', '0.271', '-0.3823', '0.2048', '-0.1652', '0.0974', '0.2717', '-0.0791', '-0.2593', '0.3635', '-0.2544', '0.0295', '-0.1561', '-0.3638', '0.108', '0.3025', '0.013885', '0.3667', '-0.07935', '0.3254', '9.286e-05', '0.3293', '0.1859', '-0.07135', '0.01489', '-0.01967', '0.01017', '0.2451', '0.671', '0.0851', '0.641', '-0.6787', '0.3306', '0.04745']",,,C536637,756.9,,,
mondo:0010014,"craniometadiaphyseal dysplasia, wormian bone type","['CRANIOMETADIAPHYSEAL dysplasia', 'Schwartz-Lelek syndrome', 'CRMDD']",,269300,85184,,,,,,,,,
mondo:0010015,anterior segment dysgenesis 7,"['PXDN anterior segment dysgenesis', 'CCMCO', 'anterior segment dysgenesis 7', 'sclerocornea with other ocular anomalies', 'COPOA', 'corneal opacification and other ocular anomalies', 'anterior segment dysgenesis 7, with sclerocornea', 'sclerocornea with Other ocular anomalies', 'corneal opacification with other ocular anomalies', 'anterior segment dysgenesis caused by mutation in PXDN', 'ASGD7', 'congenital cataract microcornea with corneal opacity', 'corneal opacification with Other ocular anomalies']",0080612,269400,289499,C3151617,"['-0.5493', '0.01677', '0.09845', '0.1301', '0.2484', '-0.0959', '-0.1372', '0.0922', '-0.407', '-0.1533', '-0.1124', '-0.1938', '0.01006', '0.07904', '-0.26', '-0.277', '0.08374', '-0.1022', '-0.04794', '-0.377', '0.1309', '0.010574', '0.05844', '0.0322', '0.1676', '0.1283', '-0.1488', '0.197', '0.05133', '0.1444', '0.238', '0.1228', '0.1471', '0.0832', '0.1951', '-0.08905', '0.03128', '-0.169', '-0.02988', '-0.2944', '0.3027', '-0.10504', '0.0854', '0.1356', '-0.251', '-0.02888', '0.1661', '0.1183', '0.226', '-0.156', '0.1508', '-0.215', '0.1531', '-0.0893', '-0.208', '-0.2042', '0.4634', '-0.0114', '-0.3665', '-0.1553', '0.05527', '-0.04004', '0.0722', '0.04852', '0.0095', '0.05826', '0.3467', '0.2402', '-0.2161', '0.02635', '-0.3325', '0.2006', '0.1774', '-0.04675', '0.01445', '-0.05978', '0.1273', '-0.01476', '-0.1539', '0.0392', '-0.0987', '-0.1234', '-0.2295', '0.313', '-0.06946', '-0.3096', '0.05652', '0.301', '0.1663', '0.1808', '0.09076', '0.339', '0.2214', '-0.005764', '0.5195', '-0.1466', '0.265', '-0.4238', '0.0897', '0.0768']",,,,,,,
mondo:0010016,sclerosteosis 1,"['sclerosteosis caused by mutation in SOST', 'SOST', 'SOST1', 'sclerosteosis type 1', 'SOST sclerosteosis', 'cortical hyperostosis with syndactyly', 'sclerosteosis 1']",0060756,269500,,CN032489,,,,,,,,
mondo:0010017,sea-blue histiocyte syndrome,"['SEA-blue histiocyte disease', 'histiocytosis, Sea-blue', 'inherited Lipemic splenomegaly', 'sea-blue histiocytosis']",4423,269600,158029,C0036489,"['-0.2437', '0.163', '0.0355', '-0.1083', '0.1048', '-0.0475', '-0.1615', '0.1128', '0.1179', '-0.02925', '-0.01428', '0.04706', '0.0756', '-0.1371', '-0.2126', '-0.2031', '-0.11395', '-0.03088', '0.0928', '-0.266', '-0.00898', '-0.2148', '0.2747', '-0.2223', '0.0772', '-0.1004', '-0.0683', '-0.1278', '-0.00322', '0.02995', '0.2091', '-0.0009403', '0.2644', '0.1826', '0.0676', '-0.1738', '-0.243', '-0.262', '-0.08527', '-0.486', '-0.06647', '-0.07007', '0.1688', '-0.244', '-0.2842', '-0.3433', '-0.01149', '0.0713', '0.3137', '-0.06995', '0.00986', '-0.0795', '0.1556', '0.2104', '-0.08057', '-0.1783', '0.2476', '-0.1882', '-0.4', '-0.02243', '0.2358', '0.0871', '-0.04117', '-0.1725', '0.01037', '-0.3025', '0.383', '0.263', '-0.1335', '0.2251', '-0.286', '-0.0507', '-0.0574', '-0.0897', '-0.03024', '0.01458', '0.1003', '0.03305', '0.0972', '-0.2191', '-0.01863', '-0.24', '0.0588', '0.1235', '-0.1183', '-0.2268', '0.1733', '0.2595', '0.05286', '-0.02354', '0.2325', '0.0954', '-0.01846', '0.01736', '0.3655', '0.2346', '0.1862', '-0.3872', '0.1527', '-0.000836']",C85062,1001170,D012618,,,,
mondo:0010018,second metatarsal-metacarpal syndrome,['second metatarsal-metacarpal syndrome'],,269630,,C1849259,,,,C564824,,,,
mondo:0010019,secretory component deficiency,"['IgA deficiency, secretory', 'secretory component deficiency']",,269650,,C0398709,,,,C562869,279.03,,,
mondo:0010020,congenital generalized lipodystrophy type 2,"['Brunzell syndrome BSCL2-related', 'congenital lipoatrophic diabetes', 'Berardinelli-Seip congenital lipodystrophy, type 2', 'lipodystrophy, congenital generalized, type 2', 'BSCL2-related Brunzell syndrome', 'CGL2', 'Berardinelli Seip congenital lipodystrophy type 2', 'Brunzell syndrome, BSCL2-related', 'Berardinelli syndrome', 'congenital generalised lipodystrophy (disease) caused by mutation in BSCL2', 'lipoatrophic diabetes, congenital', 'BSCL2 congenital generalised lipodystrophy (disease)', 'lipodystrophy, total, and acromegaloid gigantism', 'lipodystrophy, Berardinelli-Seip congenital, type 2', 'Seip syndrome', 'total lipodystrophy and acromegaloid gigantism', 'Berardinelli-Seip syndrome', 'Berardinelli-Seip congenital lipodystrophy type 2', 'BSCL2 congenital generalized lipodystrophy (disease)']",0111136,269700,,,,,,,,,,
mondo:0010021,"seizures, benign familial neonatal, autosomal recessive","['epilepsy, benign familial neonatal, autosomal recessive', 'Bfns, autosomal recessive', 'convulsions, benign familial neonatal, autosomal recessive', 'autosomal dominant form of benign neonatal seizures', 'convulsions benign familial neonatal dominant form', 'seizures, benign familial neonatal, autosomal recessive']",,269720,,C1849250,,,,C564823,,,,
mondo:0010022,senile plaque formation,['senile plaque formation'],,269800,,,,,,,,,,
mondo:0010023,combined immunodeficiency due to ZAP70 deficiency,"['immunodeficiency 48', 'STCD', 'ZAP-70 deficiency', 'IMD48', 'zeta-associated-protein 70 deficiency', 'severe combined immunodeficiency due to ZAP70 deficiency', 'selective T-cell defect']",0111943,269840,911,,"['-1.107', '0.144', '0.3823', '-0.1863', '-0.0342', '-0.1945', '0.2291', '0.1091', '0.01932', '0.1127', '0.1533', '-0.0357', '-0.07056', '-0.1654', '0.0185', '-0.3303', '0.3804', '0.312', '-0.2952', '-0.8267', '0.02103', '-0.3628', '0.524', '-0.2625', '-0.1926', '0.0525', '0.1066', '-0.3552', '-0.02892', '-0.3203', '0.2075', '0.4531', '0.3186', '0.1328', '-0.08813', '-0.1804', '-0.4768', '0.02081', '-0.1893', '-0.4473', '-0.2086', '-0.1763', '0.188', '0.001364', '-0.648', '-0.6826', '0.2177', '-0.242', '0.286', '0.2634', '0.10016', '-0.02473', '0.2708', '0.0309', '-0.5693', '0.194', '0.08356', '-0.719', '-0.311', '0.1765', '0.01865', '0.3237', '0.1199', '0.2328', '0.00524', '0.03053', '0.194', '0.3943', '-0.4558', '0.4883', '-0.343', '0.1497', '-0.11176', '-0.0359', '0.1755', '-0.02591', '0.02127', '0.10504', '0.0651', '0.014114', '-0.2166', '-0.3455', '0.1775', '0.5977', '-0.0825', '-0.339', '0.296', '0.2029', '0.3865', '-0.1743', '0.6694', '0.5557', '-0.3354', '0.125', '0.6284', '0.5825', '0.4565', '-0.6523', '-0.1307', '0.5054']",,,C536722,,,,
mondo:0010024,Beemer-Langer syndrome,"['SRTD12', 'SRPS type 4', 'short rib-polydactyly syndrome type IV', 'short rib-polydactyly syndrome type 4', 'Beemer-Langer syndrome', 'short rib-polydactyly syndrome, Beemer-Langer type', 'short rib syndrome, Beemer type', 'short rib-polydactyly syndrome Beemer type', 'Beemer Langer syndrome', 'type IV short rib polydactyly syndrome', 'Srps 4', 'short rib-polydactyly syndrome, type 4', 'short-rib thoracic dysplasia 12', 'short rib polydactyly syndrome Beemer-Langer type']",9249,269860,93268,C0432198,,,,C537599,756.9,,,
mondo:0010025,short stature-obesity syndrome,"['short stature-obesity syndrome', 'SSOS']",,269870,,C1849235,,,,C564821,,,,
mondo:0010026,SHORT syndrome,"['Aarskog-Ose-Pande syndrome', 'Rieger anomaly-partial lipodystrophy syndrome', 'short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly and teething delay', 'partial lipodystrophy with Rieger anomaly and short stature', 'short stature, hyperextensibility, hernia, ocular depression, Rieger anomaly, and teething delay', 'short syndrome', 'lipodystrophy, partial, with Rieger anomaly and short stature', 'lipodystrophy-Rieger anomaly-diabetes syndrome']",0111454,269880,3163,C0878684,"['0.1164', '0.2825', '0.141', '-0.2118', '0.3816', '-0.3923', '0.00873', '1.264', '-0.4133', '-0.2404', '0.06006', '-0.08826', '0.1492', '0.667', '-0.6', '-0.03622', '0.377', '-0.3296', '-0.06088', '-0.6353', '-0.1538', '-0.006275', '0.06198', '-0.02295', '-0.2397', '0.1239', '-0.671', '-0.009476', '0.6196', '-0.4666', '0.643', '-0.2356', '0.2678', '0.4849', '-0.0885', '0.6196', '0.313', '-0.5107', '-0.626', '-0.0661', '0.1738', '0.2122', '0.1995', '0.1863', '0.515', '-0.1877', '0.0799', '0.4558', '-0.2869', '-0.03864', '-0.1497', '0.4739', '0.249', '-0.02391', '-0.84', '-0.1575', '0.054', '-0.387', '-0.1818', '-0.0368', '0.1913', '0.3533', '-0.501', '-0.3103', '0.11597', '-0.1895', '-0.1456', '-0.09076', '0.08405', '0.1924', '0.08136', '0.0584', '-0.208', '-0.12396', '0.3625', '0.1881', '-0.10443', '-0.4536', '-0.04926', '-0.0327', '0.1906', '0.1578', '-0.01617', '0.3293', '-0.3665', '0.4756', '0.10675', '-0.532', '0.5728', '0.8643', '0.2754', '0.7285', '0.2178', '0.05963', '0.3782', '-0.3113', '0.3264', '-0.3164', '0.04733', '0.4478']",,,C537327,,,,
mondo:0010027,"free sialic acid storage disease, infantile form","['ISSD', 'sialic acid storage disorder, infantile', 'infantile sialic acid storage disease', 'N-acetylneuraminic acid storage disease', 'sialuria, infantile form', 'Nana storage disease', 'infantile free sialic acid storage disease', 'infantile sialic acid storage disorder']",,269920,309324,,"['-0.1127', '0.2493', '0.0837', '0.0161', '0.1268', '-0.2084', '-0.07996', '0.144', '-0.2056', '0.003551', '-0.1698', '-0.04498', '0.003834', '0.00011307', '-0.03604', '-0.0897', '-0.03146', '-0.02298', '-0.1198', '-0.2727', '0.013596', '-0.1265', '0.1812', '-0.00982', '-0.02162', '-0.04755', '-0.04965', '-0.04358', '-0.04446', '-0.02391', '0.1855', '0.1143', '0.2192', '0.128', '0.01046', '-0.145', '-0.05234', '-0.11383', '0.006203', '-0.1644', '0.00721', '-0.271', '0.09247', '-0.001698', '-0.1482', '-0.0817', '0.01996', '0.1116', '-0.05762', '0.1024', '-0.092', '0.005096', '0.05164', '-0.05698', '-0.11414', '-0.2157', '0.1335', '-0.03412', '-0.2198', '0.02046', '0.191', '0.06586', '0.1035', '-0.10187', '0.1052', '-0.01281', '0.2338', '-0.04892', '-0.1802', '0.04575', '-0.1302', '-0.0505', '-0.01335', '-0.05585', '0.0903', '0.1716', '0.02246', '0.004513', '-0.1422', '-0.0462', '0.000687', '0.01898', '-0.11237', '0.1088', '0.07635', '0.0419', '0.04227', '0.1262', '0.266', '0.10065', '0.1753', '0.1136', '-0.0316', '-0.03372', '0.307', '0.1962', '0.2039', '-0.2515', '-0.03784', '0.02534']",,,,,,10067532,
mondo:0010028,sialuria,"['sialuria, French type', 'sialuria']",3659,269921,3166,,"['-0.266', '0.2852', '0.0686', '-0.644', '0.00762', '-0.3525', '-0.1592', '0.5845', '-0.2922', '-0.0726', '0.05997', '0.02681', '-0.3523', '0.0714', '0.1589', '0.2515', '0.1947', '-0.08936', '-0.442', '-0.4128', '0.2015', '-0.2385', '0.1519', '-0.1025', '-0.1245', '-0.3398', '-0.02682', '-0.0648', '-0.02959', '-0.2201', '0.1142', '-0.03796', '0.4172', '0.2644', '-0.276', '-0.07043', '-0.606', '-0.2335', '-0.2703', '0.2335', '-0.1493', '-0.1808', '0.2515', '0.0914', '-0.1777', '-0.2197', '0.003286', '0.03625', '-0.1986', '0.12024', '-0.3215', '0.4014', '-0.095', '-0.002108', '0.1465', '-0.3064', '0.0363', '-0.00603', '-0.11456', '0.1401', '0.1016', '0.3916', '0.2947', '-0.1335', '0.02829', '-0.2028', '0.2181', '0.2588', '-0.5376', '0.3003', '-0.2817', '0.0321', '-0.01787', '0.185', '-0.123', '0.502', '0.338', '0.03125', '0.2075', '0.2563', '0.07886', '-0.4863', '-0.002428', '0.0906', '0.654', '0.2357', '0.04456', '0.0867', '0.342', '0.1196', '0.1089', '0.3252', '-0.1357', '-0.01996', '0.7646', '0.876', '0.2268', '-0.261', '0.4612', '0.2098']",,,,796.4,,10067529,
mondo:0010029,situs inversus,"['situs inversus totalis', 'situs ambiguus', 'laterality sequence', 'complete transposition (morphologic abnormality)', 'situs inversus totalis (disease)', 'complete situs inversus', 'complete situs inversus viscerum', 'situs inversus']",758,,101063,,"['-0.517', '-0.2493', '0.4592', '-0.294', '0.1692', '-0.0747', '-0.006905', '-0.1483', '-0.376', '-0.079', '-0.563', '-0.299', '0.1562', '0.3745', '-0.587', '-0.2269', '-0.0992', '0.077', '0.011635', '-0.7', '0.0341', '0.165', '0.5576', '-0.4612', '-0.001615', '0.0483', '0.03793', '0.4062', '0.2654', '-0.0831', '0.2986', '0.0714', '0.249', '0.2189', '0.2338', '0.0719', '0.03952', '0.2247', '0.02112', '-0.4536', '-0.0647', '0.2979', '0.2034', '0.0582', '0.0755', '-0.2096', '-0.10614', '0.3115', '-0.0801', '0.398', '-0.1353', '0.0999', '0.265', '-0.11725', '-0.3098', '-0.004734', '0.2588', '-0.1283', '-0.2125', '0.1396', '0.384', '0.3538', '-0.000866', '0.09576', '-0.09906', '-0.1089', '0.3723', '0.1412', '-0.1975', '0.1692', '-0.2092', '0.3123', '-0.01019', '-0.0804', '-0.4053', '-0.1032', '0.13', '0.1815', '-0.4656', '-0.206', '-0.2484', '0.1947', '0.354', '0.1147', '-0.2668', '-0.5503', '0.2018', '0.0551', '0.05194', '-0.4229', '0.1661', '0.2834', '0.1461', '0.1317', '0.6973', '-0.10895', '0.532', '-0.4355', '-0.02', '0.3157']",C87121,,D012857,759.89,Q89.3,,0001696
mondo:0010030,Sjogren syndrome,"['primary Sjögren syndrome', 'syndrome, Sjogren^s', 'Sjögren syndrome', 'Sjögren-Gougerot syndrome', 'xerodermosteosis', 'primary Sjogren-Gougerot syndrome', 'Sjogren^s syndrome', 'primary Sjögren-Gougerot syndrome', 'Sjogren syndrome', 'sicca syndrome']",12894,270150,378,,,C26883,0000699,D012859,710.2,,,
mondo:0010031,Sjogren-Larsson syndrome,"['fatty acid alcohol oxidoreductase deficiency', 'Sjogren-Larsson^s syndrome', 'Sjogren Larsson syndrome', 'FADH deficiency', 'FAO deficiency', 'Sjogren-Larsson syndrome', 'Sjögren-Larsson syndrome', 'fatty alcohol:NAD+ oxidoreductase deficiency', 'ichthyosis, spastic neurologic disorder, and oligophrenia', 'FALDH deficiency', 'SLS', 'fatty aldehyde dehydrogenase deficiency']",14501,270200,816,C0037231,"['0.3643', '0.6045', '0.03378', '-0.4216', '-0.1901', '-0.349', '-0.633', '0.3958', '-0.424', '-0.3252', '-0.2233', '0.3672', '0.5596', '-0.0859', '0.0646', '0.1956', '0.3582', '-0.0724', '0.0551', '-0.7676', '-0.3025', '-0.0706', '0.689', '-0.1523', '-0.528', '-0.1744', '-0.1829', '-0.09467', '-0.4556', '-0.4539', '0.772', '-0.516', '0.03363', '0.05963', '-0.7437', '0.03436', '-0.1249', '-0.785', '-0.2075', '0.0672', '-0.014946', '-0.4238', '-0.09204', '0.861', '0.3555', '0.1448', '0.4556', '-0.10693', '0.6343', '-0.0424', '-0.5894', '0.002035', '-0.061', '-0.3484', '-0.2397', '-0.08826', '1.28', '0.2145', '-0.3042', '-0.02928', '0.4253', '-0.014915', '0.31', '0.2405', '-0.06226', '0.06183', '0.4136', '0.3083', '-0.06604', '0.3845', '0.2335', '0.1445', '-0.2053', '0.1306', '0.1504', '0.09564', '0.1956', '-0.674', '0.2035', '0.2307', '0.05136', '-0.2489', '-0.1602', '0.882', '0.2104', '0.2634', '-0.3125', '0.10364', '0.4797', '0.666', '0.448', '0.3728', '0.07184', '0.11896', '0.0405', '-0.4956', '0.4692', '-0.12006', '0.3406', '-0.2181']",C85070,0007031,D016111,,,10048676,
mondo:0010032,Sjogren-Larsson-like ichthyosis without CNS or eye involvement,"['Sjogren-Larsson-like ichthyosis without CNS or eye involvement', 'ichthyosis, Sjogren-Larsson-like, without CNS or eye involvement', 'Sjogren-Larsson-like syndrome']",,270220,,C1849195,,,,C536668,,,,
mondo:0010033,generalized peeling skin syndrome,"['generalised PSS', 'peeling skin syndrome type 1', 'generalised deciduous skin', 'generalized deciduous skin', 'PSS1', 'peeling skin syndrome 1', 'generalized PSS']",,,263543,CN202304,"['0.2776', '0.1317', '-0.1658', '-0.2115', '0.3242', '-0.541', '-0.2223', '-0.266', '-0.3438', '0.5005', '-0.287', '-0.01472', '-0.5386', '-0.002522', '-0.3362', '0.1062', '0.0393', '-0.4187', '0.04276', '-0.8823', '-0.3647', '0.02261', '0.8013', '-0.447', '0.2778', '0.3047', '-0.04196', '-0.4817', '-0.2266', '-0.3408', '-0.06006', '0.1858', '0.1196', '0.11365', '0.603', '0.2119', '-0.7993', '-0.1186', '-0.4597', '-0.3928', '0.1663', '-0.92', '0.08057', '0.04385', '0.3354', '-0.0887', '-0.8647', '0.7046', '0.2869', '-0.394', '0.2507', '-0.5996', '0.593', '0.02298', '-0.608', '-0.3032', '0.3489', '-0.03363', '-0.8354', '-0.683', '-0.3325', '-0.11237', '-0.0087', '-0.01982', '0.1127', '0.2961', '0.582', '0.135', '-0.5283', '0.8213', '-0.3032', '-0.3276', '0.2108', '0.01444', '0.1036', '0.2017', '-0.1139', '0.4338', '-0.1772', '-0.382', '0.2415', '-0.1742', '-0.2778', '-0.3271', '0.09644', '-0.4172', '0.049', '0.77', '0.4937', '-0.2761', '0.758', '0.2712', '0.773', '0.4446', '0.601', '0.2793', '-0.05835', '-0.5312', '0.1133', '-0.12134']",,,,,,,
mondo:0010035,Smith-Lemli-Opitz syndrome,"['Smith-Lemli-Opitz syndrome', 'Rutledge lethal multiple congenital anomaly syndrome', 'Smith-Opitz-inborn syndrome', 'polydactyly, sex reversal, renal hypoplasia, and unilobular lung', 'SLOS', 'RSH syndrome', 'Smith Lemli Opitz syndrome', 'SLO syndrome', 'polydactyly, sex reversal, renal hypoplasia, and unilobar lung', '7-dehydrocholesterol reductase deficiency', 'lethal acrodysgenital syndrome']",14692,270400,818,C0175694,"['-0.4724', '0.06177', '0.3406', '-0.822', '0.2332', '-0.06146', '-0.02437', '0.724', '-0.7827', '-1.093', '-0.3608', '-0.451', '-0.1142', '-0.1071', '-0.601', '-0.12274', '0.1685', '-0.2554', '-0.618', '1.92e-05', '0.12305', '-0.327', '0.3933', '-0.1147', '0.4197', '-0.3613', '0.4016', '0.2285', '0.4995', '-0.6006', '0.4905', '-0.2737', '0.611', '0.467', '0.06122', '-0.3694', '0.3315', '-0.277', '-0.1251', '0.2834', '0.11334', '0.1436', '0.4944', '0.1788', '0.03796', '-0.1469', '0.595', '0.6875', '-0.1492', '0.4126', '-0.4202', '0.03812', '-0.2969', '-0.525', '-0.4604', '0.04044', '0.4775', '-0.3623', '-0.1365', '0.355', '0.1283', '0.6084', '0.05066', '0.3196', '0.1302', '0.2837', '-0.1196', '0.02701', '0.09454', '0.2983', '-0.5083', '0.2341', '-0.1359', '0.0922', '-0.01709', '0.286', '0.4749', '-0.7837', '-0.9556', '0.1493', '-0.01032', '-0.4067', '0.0836', '0.306', '0.305', '0.113', '0.0654', '0.1054', '-0.1969', '0.1589', '-0.554', '0.427', '0.05804', '-0.535', '0.595', '0.01688', '0.3704', '-0.235', '0.07324', '0.2413']",C85071,,D019082,759.89,E78.72,,
mondo:0010036,congenital secretory sodium diarrhea 3,"['diarrhea 3, secretory sodium, congenital, syndromic', 'DIAR3', 'diarrhea 3, secretory sodium, congenital, with or without other congenital anomalies', 'congenital secretory sodium diarrhea 3 with or without other congenital anomalies', 'congenital secretory sodium diarrhea 3 syndromic', 'congenital secretory sodium diarrhoea 3 with or without other congenital anomalies', 'congenital secretory sodium diarrhoea type 3', 'congenital secretory sodium diarrhea type 3', 'secretory diarrhea caused by mutation in SPINT2', 'secretory diarrhoea caused by mutation in SPINT2', 'diarrhoea 3, secretory sodium, congenital, syndromic', 'diarrhoea 3, secretory sodium, congenital, with or without other congenital anomalies', 'sodium diarrhea, congenital', 'congenital secretory sodium diarrhoea 3 syndromic', 'SPINT2 secretory diarrhea', 'SPINT2 secretory diarrhoea']",0060781,270420,,,,,,,,,,
mondo:0010037,sodium-potassium-ATPase activity of red cell,"['sodium pump sites, number of', 'sodium-potassium-ATPase activity of red cell']",,270425,,,,,,,,,,
mondo:0010038,growth delay due to insulin-like growth factor I resistance,"['resistance to IGF-1', 'Somatomedin-c resistance to', 'Somatomedin-C, resistance to', 'insulin-like growth factor 1 resistance to', 'insulin-like Growth Factor I, resistance to, due to increased binding Protein', 'insulin-like growth factor I, resistance to', 'IGF1RES', 'IGF-I resistance', 'Somatomedin, end-organ insensitivity to', 'IGF-1 resistance', 'Somatomedin end-organ insensitivity to']",,270450,73273,C1849157,"['-0.2793', '-0.1392', '0.377', '-0.4844', '0.03522', '0.01817', '0.3662', '0.8413', '-0.778', '-0.75', '0.08246', '-0.03067', '0.1957', '-0.1626', '-0.499', '0.339', '0.4392', '-0.1564', '-0.7295', '-0.54', '0.63', '-0.2301', '0.2815', '0.0909', '0.5034', '0.2812', '0.0752', '-0.05563', '0.2656', '-0.5835', '0.7124', '0.0996', '0.348', '0.1228', '-0.3093', '-0.3223', '-0.2467', '-0.3184', '-0.1581', '-0.534', '0.2947', '-0.0794', '0.09326', '0.406', '-0.1019', '-0.3855', '0.6416', '0.0428', '0.0644', '0.1605', '-0.583', '-0.715', '-0.153', '0.3027', '-0.432', '0.1407', '-0.1053', '-0.6987', '-0.2446', '0.8857', '0.0422', '-0.0821', '-0.3682', '-0.1323', '-0.0375', '0.02994', '-0.1902', '0.5464', '-0.0905', '0.3445', '-0.836', '0.2268', '-0.05524', '0.2333', '0.1978', '0.2898', '0.4976', '-0.5405', '-0.014175', '-0.02043', '0.306', '0.05566', '-0.299', '0.1422', '-0.262', '0.3281', '-0.3115', '0.2563', '0.5396', '0.4312', '0.1327', '-0.1594', '-0.4744', '-0.2856', '0.671', '0.0883', '-0.0987', '-0.624', '0.3623', '0.1888']",,,C564816,,,,
mondo:0010039,congenital heart defect-round face-developmental delay syndrome,"['Sonoda syndrome', 'round face with depressed nasal Bridge and small mouth, congenital heart defect, and retarded development']",,270460,1355,C0796162,,,,C536680,,,,
mondo:0010040,"ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability","['ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and intellectual disability', 'ataxia, spastic, childhood-onset, autosomal recessive, with optic atrophy and mental retardation']",,270500,,C3151619,,,,,,,,
mondo:0010041,Charlevoix-Saguenay spastic ataxia,"['sacs', 'autosomal recessive spastic ataxia of Charlevoix-Saguenay', 'spastic ataxia 6, autosomal recessive', 'autosomal recessive spastic ataxia type 6', 'Charlevoix-Saguenay spastic ataxia', 'ARSACS', 'spastic ataxia of Charlevoix-Saguenay', 'SPAX6', 'spastic ataxia Charlevoix-Saguenay type', 'spastic ataxia, Charlevoix-Saguenay type']",0050946,270550,98,C1849140,"['-0.06366', '-0.10706', '-0.2119', '0.1318', '-0.3237', '-0.6978', '0.08453', '0.3691', '-0.5273', '-0.8125', '0.06064', '0.1193', '-0.094', '0.2546', '0.369', '-0.254', '-0.1825', '-0.307', '0.2338', '-0.8574', '-0.04364', '-0.2537', '0.1345', '-0.4138', '0.2842', '-0.3972', '-0.501', '0.2585', '-0.0892', '-0.6836', '0.219', '0.1244', '-0.642', '-0.2106', '0.34', '0.07294', '0.069', '0.264', '0.3853', '0.6147', '0.0409', '0.0984', '-0.427', '0.353', '0.4963', '-0.5225', '0.1862', '0.3218', '0.3064', '0.08215', '-0.2213', '0.309', '-0.0814', '-0.4055', '0.08527', '-0.7124', '0.4998', '0.4482', '-0.1328', '0.279', '-0.5225', '0.2499', '0.2026', '-0.12103', '-0.1768', '0.4868', '0.3713', '0.4233', '-0.6113', '0.3918', '0.6157', '0.5356', '-0.05527', '-0.753', '0.5938', '0.3733', '0.2646', '0.1844', '0.181', '0.4553', '-0.4187', '-0.957', '0.4062', '0.833', '-0.2135', '-0.525', '0.3079', '-0.1744', '0.4033', '0.2708', '0.471', '0.5146', '-0.07837', '-0.1967', '0.9204', '0.6357', '0.3447', '0.578', '-0.208', '0.1395']",,,C536787,,,,
mondo:0010042,spastic diplegia and intellectual disability,"['hereditary spastic diplegia with mental retardation', 'spastic diplegia and intellectual disability', 'hereditary spastic diplegia with intellectual disability', 'spastic diplegia and mental retardation', 'spastic diplegia, infantile type', 'spastic diplegia infantile type']",,270600,,C1849139,,,,C537481,,,,
mondo:0010043,hereditary spastic paraplegia 17,"['spastic paraplegia 17', 'hereditary spastic paraplegia caused by mutation in BSCL2', 'spastic paraplegia with amyotrophy of hands and feet', 'BSCL2 hereditary spastic paraplegia', 'hereditary spastic paraplegia type 17', 'spastic paraplegia-amyotrophy of hands and feet', 'Silver spastic paraplegia syndrome', 'Silver syndrome', 'autosomal dominant spastic paraplegia type 17', 'spastic paraplegia 17, autosomal dominant', 'dHMN5B', 'distal hereditary motor neuropathy type 5B', 'autosomal dominant spastic paraplegia 17', 'SPG17']",0110770,270685,100998,CN074197,"['-0.2524', '0.1846', '-0.12164', '-0.32', '-0.3022', '-0.698', '-0.2966', '0.02803', '-0.5137', '-0.5083', '0.0867', '-0.02344', '-0.106', '0.276', '0.7935', '0.2333', '-0.3582', '-0.2435', '0.03882', '-0.3757', '0.3525', '-0.1383', '0.2239', '0.2883', '0.009575', '0.127', '0.188', '0.01377', '-0.255', '-0.1799', '0.2001', '0.1691', '0.0439', '0.2676', '0.2986', '-0.414', '-0.0367', '-0.1622', '-0.12463', '-0.4', '0.01441', '-0.6206', '-0.2737', '0.2805', '0.05545', '-0.5527', '-0.3389', '0.3975', '0.047', '0.1376', '-0.09827', '0.001751', '-0.3674', '-0.2654', '-0.1869', '-0.7217', '0.7593', '-0.05206', '-0.3557', '0.3862', '-0.1033', '-0.0953', '0.3115', '0.2986', '-0.6934', '0.1161', '0.2947', '0.5674', '-0.1592', '0.672', '-0.2556', '-0.188', '0.0839', '-0.4866', '0.95', '0.4382', '-0.2319', '0.1785', '-0.11707', '-0.11646', '0.07294', '-0.2595', '0.749', '0.929', '-0.1846', '-0.2029', '0.1412', '0.3257', '0.05392', '-0.001259', '0.6294', '-0.1787', '0.2295', '0.1741', '0.928', '0.5', '0.4858', '-0.05743', '-0.2058', '0.03467']",,,C536644,,,,
mondo:0010044,hereditary spastic paraplegia 15,"['Kjellin syndrome', 'spastic paraplegia and retinal degeneration', 'spastic paraplegia-retinal degeneration syndrome', 'hereditary spastic paraplegia type 15', 'autosomal recessive complex spastic paraplegia caused by mutation in ZFYVE26', 'ZFYVE26 autosomal recessive complex spastic paraplegia', 'spastic paraplegia 15, autosomal recessive', 'spastic paraplegia 15', 'hereditary spastic paraparesis type 15', 'recessive spastic paraplegia with retinal degeneration', 'spastic paraplegia and retinal Degeneration', 'autosomal recessive spastic paraplegia 15', 'autosomal recessive spastic paraplegia type 15', 'SPG15']",0110768,270700,100996,C1849128,"['-0.4727', '0.06195', '-0.0882', '-0.6064', '-0.2512', '-0.581', '-0.3918', '0.4177', '-0.7812', '-0.10126', '-0.2346', '0.1226', '-0.0858', '-0.4265', '0.3838', '-0.425', '-0.02832', '-0.3867', '0.1514', '-0.449', '0.1159', '0.0237', '0.1426', '0.2842', '0.3376', '0.2009', '0.0962', '-0.1147', '-0.0321', '-0.0682', '0.006573', '-0.0282', '0.299', '0.2184', '-0.05194', '-0.10474', '-0.4236', '-0.2817', '-0.2698', '-0.2944', '0.296', '-0.64', '-0.2192', '0.505', '-0.2847', '-0.32', '-0.2102', '0.1837', '0.3264', '-0.119', '0.4255', '0.3606', '-0.544', '-0.4087', '-0.328', '-0.4788', '0.4797', '-0.392', '-0.1873', '0.3079', '-0.1487', '0.1927', '0.463', '0.462', '-0.6235', '0.0713', '0.2568', '0.825', '-0.10846', '0.4001', '-0.2163', '0.3545', '0.08856', '-0.1207', '0.4844', '0.2766', '0.1548', '-0.02353', '0.1768', '-0.05307', '-0.010635', '-0.2375', '0.3035', '1.074', '-0.01281', '0.09375', '0.0142', '0.3213', '0.3467', '0.02548', '0.2279', '0.5444', '0.0644', '0.3457', '0.791', '0.2379', '0.592', '-0.0724', '-0.05594', '0.743']",,,C536642,,,,
mondo:0010046,hereditary spastic paraplegia 23,"['spastic paraplegia vitiligo premature graying and characteristic facies', 'spastic paraparesis-vitiligo-premature graying-characteristic facies syndrome', 'spastic paraparesis, vitiligo, premature graying, characteristic facies', 'spastic paraplegia vitiligo premature greying and characteristic facies', 'Lison syndrome', 'DSTYK autosomal recessive complex spastic paraplegia', 'spastic paraplegia 23', 'autosomal recessive complex spastic paraplegia caused by mutation in DSTYK', 'spastic paraplegia with pigmentary abnormalities', 'hereditary spastic paraplegia type 23', 'autosomal recessive spastic paraplegia type 23', 'spastic paraplegia and pigmentary abnormalities', 'SPG 23', 'SPG23']",0110774,270750,101003,C0796019,"['-0.007145', '0.1589', '-0.00903', '-0.2703', '-0.0002034', '-0.4329', '-0.6772', '-0.1749', '-0.2996', '-0.2766', '0.01366', '-0.2211', '0.0836', '0.1575', '0.4927', '0.2922', '0.1984', '-0.2074', '0.3813', '-0.3845', '0.03986', '-0.2208', '0.2798', '0.04343', '0.1674', '0.2632', '-0.01933', '-0.02557', '-0.001131', '-0.2163', '0.571', '0.098', '0.04544', '0.1069', '0.2301', '-0.08325', '-0.2637', '-0.2642', '-0.1526', '-0.4597', '0.2472', '-0.6553', '-0.3', '0.33', '0.06116', '-0.4944', '-0.2966', '0.3347', '-0.0991', '-0.2023', '0.00853', '0.11395', '-0.2152', '-0.0904', '0.02231', '-0.7603', '0.7197', '-0.0961', '-0.2864', '-0.00837', '-0.2532', '-0.08154', '0.1288', '0.3596', '-0.259', '0.0659', '0.4956', '0.6885', '-0.2356', '0.709', '-0.471', '-0.459', '0.3586', '-0.1589', '0.576', '0.2517', '-0.4329', '-0.0829', '-0.002947', '-0.4873', '0.3923', '-0.3542', '0.4363', '0.7075', '-0.1733', '-0.2053', '0.0732', '0.376', '0.1499', '-0.00922', '0.422', '0.2194', '0.3909', '0.462', '0.8247', '0.1682', '0.3281', '0.1909', '0.2137', '-0.1921']",,,C536859,,,,
mondo:0010047,hereditary spastic paraplegia 5A,"['spastic paraplegia 5A', 'CYP7B1 pure or complex autosomal recessive spastic paraplegia', 'spastic paraplegia type 5A', 'spastic paraplegia type 5B, recessive', 'autosomal recessive spastic paraplegia type 5A', 'autosomal recessive spastic paraplegia', 'hereditary spastic paraplegia type 5A', 'pure or complex autosomal recessive spastic paraplegia caused by mutation in CYP7B1', 'spastic paraplegia 5A, autosomal recessive', 'SPG5A', 'autosomal recessive spastic paraplegia 5A']",0110810,270800,100986,C2931357,"['-0.08636', '0.2145', '-0.658', '-0.1737', '0.01988', '-0.76', '-0.334', '-0.014496', '-0.631', '-0.3184', '-0.447', '-0.172', '-0.3809', '0.2505', '0.821', '0.1627', '-0.4165', '-0.7437', '0.2369', '-0.2491', '0.3088', '-0.2207', '0.6035', '-0.1959', '-0.02184', '-0.2472', '0.1137', '0.0959', '-0.3242', '-0.1898', '0.448', '0.04404', '0.1044', '0.1571', '0.2092', '-0.35', '-0.607', '-0.0338', '-0.1376', '-0.49', '0.2118', '-0.4412', '-0.06323', '0.3499', '-0.1581', '-0.456', '-0.2913', '0.23', '-0.1057', '0.143', '0.3933', '0.1714', '-0.4111', '-0.3655', '-0.2247', '-0.382', '0.683', '0.1508', '-0.1875', '0.371', '-0.168', '-0.09454', '0.4084', '0.08636', '-0.961', '0.5405', '0.4722', '0.9746', '-0.01307', '0.54', '-0.068', '0.1556', '-0.03714', '-0.2969', '0.885', '0.07526', '0.0401', '-0.03687', '-0.0986', '-0.3167', '-0.191', '-0.2385', '0.614', '1.296', '-0.01436', '0.1863', '0.33', '0.2152', '0.364', '-0.2837', '0.5195', '0.4236', '0.146', '0.509', '0.699', '0.4885', '0.755', '0.5234', '0.2583', '0.0891']",,,,,,,
mondo:0010048,spastic paraplegia with myoclonic epilepsy,['spastic paraplegia with myoclonic epilepsy'],,270805,,C1849114,,,,C564810,,,,
mondo:0010049,spastic paraplegia-glaucoma-intellectual disability syndrome,"['spastic paresis glaucoma mental retardation', 'spastic paresis, glaucoma, and mental retardation', 'spastic paresis, glaucoma, and intellectual disability', 'spastic paresis glaucoma intellectual disability']",,270850,2818,C1849113,,,,C564809,,,,
mondo:0010051,spastic tetraplegia-retinitis pigmentosa-intellectual disability syndrome,"['progressive quadriparesis, intellectual disability, retinitis pigmentosa and hearing loss', 'spastic quadriplegia, retinitis pigmentosa, and intellectual disability', 'spastic quadriplegia-retinitis pigmentosa-intellectual disability syndrome', 'spastic quadriplegia retinitis pigmentosa intellectual disability', 'spastic quadriplegia retinitis pigmentosa mental retardation', 'progressive quadriparesis, mental retardation, retinitis pigmentosa and hearing loss', 'spastic quadriplegia, retinitis pigmentosa, and mental retardation']",,270950,3011,C1849112,,,,C564808,,,,
mondo:0010052,spermatogenic failure 4,"['spermatogenic failure type 4', 'pregnancy loss, recurrent, susceptibility to, 4', 'SPGF4', 'azoospermia caused by mutation in SYCP3', 'arrest of spermatogenesis', 'azoospermia due to Perturbations of meiosis', 'spermatogenesis arrest', 'spermatogenic failure 4', 'pregnancy loss, recurrent, 4', 'azoospermia with maturation arrest', 'SYCP3 azoospermia']",0070176,270960,,,,,,C536875,,,,
mondo:0010053,hereditary spherocytosis type 3,"['HS3', 'hereditary spherocytosis 3', 'spherocytosis, type 3', 'SPTA1 hereditary spherocytosis', 'hereditary spherocytosis caused by mutation in SPTA1', 'spherocytosis, hereditary, 3', 'SPH3']",0110918,270970,,C2678338,,,,C567489,,,,
mondo:0010054,spinal muscular atrophy with intellectual disability,"['spinal muscular atrophy with mental retardation', 'spinal muscular atrophy with intellectual disability']",,271109,,C1849109,,,,C564807,,,,
mondo:0010055,spinal muscular atrophy with microcephaly and mental subnormality,['spinal muscular atrophy with microcephaly and mental subnormality'],,271110,,C1849108,,,,C564806,,,,
mondo:0010056,"spinal muscular atrophy, type IV","['SMA type IV', 'adult spinal muscular atrophy', 'spinal muscular atrophy-4', 'adult-onset spinal muscular atrophy', 'SMA type 4', 'SMA4', 'spinal muscular atrophy, type IV', 'SMA 4', 'spinal muscular atrophy, proximal, adult, autosomal recessive', 'spinal muscular atrophy, type 4', 'spinal muscular atrophy, adult form', 'SMA-IV', 'spinal muscular atrophy of adults', 'spinal muscular atrophy type 4', 'proximal spinal muscular atrophy type 4', 'spinal muscular atrophy 4']",0050529,271150,83420,,"['-0.1805', '-0.12463', '0.06232', '0.1168', '0.1743', '-0.7183', '0.6616', '0.9966', '-1.306', '-0.1973', '-0.306', '0.1434', '-0.08716', '0.902', '0.558', '-0.673', '-0.4897', '-0.6963', '-0.177', '-0.809', '-0.01907', '-0.6787', '0.6465', '0.09485', '-0.2496', '-0.2837', '0.04657', '0.0516', '-0.97', '0.1371', '0.2883', '0.3088', '-0.537', '-0.2405', '-0.1826', '-0.4062', '0.1744', '0.0758', '0.4905', '0.09314', '-0.4192', '-0.711', '-0.3062', '0.4067', '0.2805', '0.282', '-0.2505', '-0.08606', '-0.03195', '-0.01079', '0.05435', '-0.5054', '-0.2214', '-0.57', '-0.2374', '-0.4048', '0.4534', '-0.2213', '-0.0748', '0.1179', '0.0951', '0.3645', '0.2115', '0.2443', '-0.741', '0.547', '0.06476', '0.3052', '0.2305', '-0.2166', '-0.1123', '-0.0699', '0.0947', '-0.1989', '0.3953', '0.3018', '-0.2306', '-0.1356', '-0.3591', '-0.5713', '0.5884', '-0.0677', '-0.375', '0.96', '-0.4844', '0.4905', '0.003578', '0.3215', '0.56', '0.15', '0.2487', '-0.2703', '-0.2317', '0.121', '0.4956', '-0.1048', '0.673', '-0.3467', '0.10895', '-0.2172']",,,C563948,335.19,,,
mondo:0010057,"spinal muscular atrophy, Ryukyuan type","['spinal muscular atrophy, Ryukyuan type', 'spinal muscular atrophy Ryukyuan type', 'Ryukyuan muscular atrophy']",,271200,,C1849102,,,,C536881,,,,
mondo:0010058,"scapuloperoneal spinal muscular atrophy, autosomal recessive","['spinal muscular atrophy, scapuloperoneal']",,271220,,CN074295,,,,,,,,
mondo:0010060,mitochondrial DNA depletion syndrome 7 (hepatocerebral type),"['ophthalmoplegia-hypotonia-ataxia-hypoacusis-athetosis syndrome', 'infantile onset spinocerebellar ataxia', 'ophthalmoplegia, hypotonia, ataxia, hypacusis, and athetosis', 'spinocerebellar ataxia 8', 'ophthalmoplegia - hypotonia - ataxia - hypoacusis - athetosis', 'MTDPS7', 'mitochondrial DNA depletion syndrome 7 (hepatocerebral type)', 'mitochondrial DNA depletion syndrome 7', 'SCA8 (formerly)', 'spinocerebellar ataxia, infantile, with sensory neuropathy', 'spinocerebellar ataxia infantile with sensory neuropathy', 'Ohaha syndrome', 'spinocerebellar ataxia 8, formerly', 'spinocerebellar ataxia 8 (formerly)', 'OHAHA syndrome', 'TWNK autosomal recessive degenerative and progressive cerebellar ataxia', 'IOSCA', 'spinocerebellar ataxia, infantile-onset', 'ophthalmoplegia, hypotonia, ataxia, hypoacusis, and athetosis', 'mitochondrial DNA depletion syndrome type 7']",0080126,271245,1186,C1849096,"['0.02943', '-0.2362', '0.02094', '0.1207', '-0.1234', '-0.655', '0.2761', '0.4475', '-0.6143', '-0.9043', '-0.01756', '0.1388', '-0.07965', '0.2372', '0.3154', '-0.2847', '-0.2869', '-0.3', '0.05276', '-0.745', '-0.1251', '-0.3142', '0.09265', '-0.547', '0.03958', '-0.5723', '-0.2998', '0.1084', '-0.010666', '-0.9526', '0.1599', '0.3618', '-0.4138', '-0.08453', '0.3784', '-0.0971', '0.0543', '0.1175', '0.4043', '0.684', '0.1891', '0.014046', '-0.0971', '0.4324', '0.5786', '-0.764', '-0.004158', '0.2125', '0.297', '-0.0517', '-0.303', '0.08215', '0.10474', '-0.2659', '-0.0724', '-0.5884', '0.3586', '0.506', '-0.08295', '0.4177', '-0.4233', '0.1732', '0.1792', '0.06116', '-0.4102', '0.5146', '0.2058', '0.332', '-0.553', '0.11383', '0.5864', '0.501', '-0.1323', '-0.636', '0.6274', '0.2303', '0.335', '0.2117', '0.0994', '0.4094', '-0.05237', '-0.8813', '0.2246', '0.774', '-0.2783', '-0.6426', '0.224', '-0.0239', '0.4153', '0.4954', '0.3772', '0.359', '0.1857', '-0.05872', '0.839', '0.692', '0.4707', '0.2925', '-0.1475', '0.0734']",,,C535523,,,,
mondo:0010061,autosomal recessive cerebellar ataxia-blindness-deafness syndrome,"['spinocerebellar ataxia, autosomal recessive 3', 'SCAR3', 'SCABD', 'autosomal recessive spinocerebellar ataxia-blindness-deafness syndrome', 'spinocerebellar ataxia with blindness and deafness', 'spinocerebellar ataxia autosomal recessive 3', 'autosomal recessive spinocerebellar ataxia-blindness-hearing loss syndrome', 'autosomal recessive spinocerebellar ataxia type 3', 'autosomal recessive cerebellar ataxia - blindness - deafness']",0111612,271250,95433,C1849094,,,,C537309,,,,
mondo:0010062,spinocerebellar ataxia-dysmorphism syndrome,['spinocerebellar ataxia with dysmorphism'],,271270,1185,C1849088,,,,C564802,,,,
mondo:0010063,corneal-cerebellar syndrome,"['spinocerebellar degeneration corneal dystrophy', 'corneal cerebellar syndrome', 'Der Kaloustian-Jarudi-Khoury syndrome', 'corneal-cerebellar syndrome', 'spinocerebellar degeneration-corneal dystrophy syndrome', 'Der Kaloustian Jarudi Khoury syndrome', 'corneal dystrophy with spinocerebellar Degeneration', 'spinocerebellar degeneration and corneal dystrophy']",,271310,3177,C1849087,,,,C535472,,,,
mondo:0010064,spastic ataxia-corneal dystrophy syndrome,"['Mousa Al din Al Nassar syndrome', 'spinocerebellar degeneration with macular corneal dystrophy, congenital cataracts, and myopia', 'spastic ataxia, macular corneal dystrophy, congenital cataracts, myopia and vertically oval temporally tilted disks', 'spastic ataxia, macular corneal dystrophy, congenital cataracts, myopia and vertically oval temporally tilted discs', 'Mousa-Al Din-Al Nassar syndrome', 'spastic ataxia-ocular anomalies syndrome', 'Bedouin spastic ataxia syndrome']",,271320,2572,C1849085,,,,C536989,,,,
mondo:0010065,spinocerebellar degeneration with slow eye movements,"['SDSEM', 'spinocerebellar degeneration with slow eye movements']",,271322,,,,,,,,,,
mondo:0010066,familial isolated congenital asplenia,"['asplenia, familial', 'ICAS', 'asplenia, isolated congenital', 'hyposplenia, isolated congenital', 'splenic hypoplasia']",,271400,101351,,"['-0.678', '-0.1687', '-0.545', '-0.3308', '-0.10394', '-0.1727', '-0.3367', '0.4802', '-0.4077', '-0.1366', '-0.04764', '-0.0956', '-0.1451', '-0.003725', '-0.2578', '0.227', '-0.1852', '0.3235', '-0.2861', '-0.7524', '0.1638', '-0.01081', '0.9565', '-0.0809', '0.3127', '0.1969', '-0.2893', '0.4634', '-0.03232', '-0.385', '0.558', '-0.1642', '0.2722', '-0.261', '-0.03528', '0.3953', '-0.436', '-0.06104', '0.209', '-0.4695', '0.055', '-0.1837', '0.312', '-0.2004', '-0.3545', '-0.05585', '-0.675', '-0.1053', '0.02246', '0.2976', '0.03268', '0.06033', '0.319', '0.0831', '-0.3828', '-0.00721', '0.1476', '-0.2998', '-0.02881', '0.4648', '0.2952', '0.2417', '0.317', '-0.0902', '0.2827', '0.05182', '0.02768', '0.1451', '-0.546', '0.4463', '0.0757', '0.1991', '-0.4097', '-0.1449', '-0.1593', '-0.958', '0.7144', '0.2202', '0.058', '-0.328', '-0.6567', '-0.3584', '-0.09515', '-0.3777', '-0.1652', '-0.1827', '0.1583', '0.06824', '0.1289', '0.07306', '-0.007114', '-0.0838', '-0.1979', '-0.2043', '0.762', '0.1447', '0.4436', '-0.7', '0.2568', '-0.00272']",,,C563028,,,,
mondo:0010067,splenoportal vascular anomalies,['splenoportal vascular anomalies'],,271500,,,,,,C562761,,,,
mondo:0010068,"spondyloepimetaphyseal dysplasia, sponastrime type","['spondylar and nasal changes with striations of the metaphyses (SPONASTRIME) dysplasia', 'spondylar and nasal alterations-striated metaphyses syndrome', 'short-limb dwarfism with saddle Nose, spinal alterations, and metaphyseal striation', 'spondylar and nasal alterations with striated metaphyses', 'short limb dwarfism with saddle nose, spinal alterations, and metaphyseal striation', 'Sponastrime dysplasia', 'sponastrime dysplasia', 'spondyloepimetaphyseal dysplasia, Sponastrime type', 'spondyloepimetaphyseal dysplasia, sponastrime type', 'spondylar and nasal changes with triations of the metaphyses (SPONASTRIME) dysplasia', 'spondyloepimetaphyseal dysplasia Sponastrime type']",5684,271510,93357,,"['-0.545', '0.2054', '0.5244', '-0.726', '0.0762', '-0.1239', '0.0797', '0.832', '-0.6045', '-0.0457', '-0.08887', '-0.0939', '-0.2435', '-0.1526', '-0.02466', '0.11646', '0.6', '-0.03001', '-0.3547', '-0.3943', '-0.0828', '-0.0647', '0.4978', '-0.266', '0.2471', '0.10846', '0.011566', '-0.3477', '0.2156', '-0.3413', '0.0552', '0.00823', '0.1564', '0.1293', '0.306', '-0.1829', '-0.4502', '-0.424', '0.0363', '-0.6562', '-0.0609', '-0.2285', '0.0976', '0.05048', '-0.007183', '-0.6016', '-0.1896', '0.4553', '0.2693', '-0.00687', '0.1505', '0.1791', '0.1874', '0.1958', '-0.528', '-0.875', '-0.2214', '-0.134', '0.02646', '0.03787', '0.4077', '0.1017', '-0.3606', '-0.1847', '-0.12115', '-0.1259', '0.328', '0.5674', '-0.1383', '0.4675', '-0.265', '0.1583', '0.2255', '-0.123', '-0.543', '0.1527', '0.07605', '0.1005', '-0.1566', '-0.06244', '-0.1532', '-0.1919', '0.1674', '0.572', '-0.396', '0.3823', '-0.1053', '0.1425', '0.304', '0.304', '-0.317', '0.1443', '-0.01845', '0.1648', '0.661', '0.0327', '0.7554', '-0.2676', '0.2869', '0.1846']",C129031,,C535786,756.9,,,
mondo:0010069,spondylocostal dysostosis-anal and genitourinary malformations syndrome,"['CMn syndrome', 'spondylocostal dysostosis-anal atresia-genitourinary malformation syndrome', 'Casamassima-Morton-Nance syndrome', 'spondylocostal dysostosis with anal atresia and urogenital anomalies']",,271520,94095,C1849069,,,,C564799,,,,
mondo:0010070,"brachyolmia type 1, Hobaek type","['brachyolmia type 1, Hobaek type', 'spondylodysplasia with Pure brachyolmia', 'BCYM1A', 'brachyolmia, recessive type of Hobaek']",,271530,93301,C1849055,,,,C537099,,,,
mondo:0010072,"spondyloepiphyseal dysplasia tarda, autosomal recessive","['autosomal recessive spondyloepiphyseal dysplasia tarda', 'spondyloepiphyseal dysplasia tarda, autosomal recessive']",0112293,271600,,C1849054,,,,C564797,,,,
mondo:0010073,"spondyloepiphyseal dysplasia tarda, Kohn type","['spondyloepiphyseal dysplasia tarda with intellectual disability', 'Sedt with mental retardation', 'spondyloepiphyseal dysplasia tarda with mental retardation', 'Sedt with intellectual disability']",0112292,271620,163665,C1849053,,,,C564796,,,,
mondo:0010074,"brachyolmia type 1, toledo type","['PAPS-chondroitin sulphate sulfotransferase deficiency', 'BCYM1B', 'Sed, chondroitin sulphate type', 'brachyolmia type 1, Toledo type', 'PAPS-chondroitin sulfate sulfotransferase deficiency', 'Sed, chondroitin sulfate type', 'spondyloepiphyseal dysplasia tarda, Toledo type']",,271630,93303,C1849048,,,,C535787,,,,
mondo:0010075,"spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures","['B3GALT6 spondyloepimetaphyseal dysplasia with joint laxity', 'spondyloepimetaphyseal dysplasia with joint laxity caused by mutation in B3GALT6', 'spondyloepimetaphyseal dysplasia with joint laxity, Beighton type', 'spondyloepimetaphyseal dysplasia with JOINT laxity, type 1, with or without fractures', 'SEMDJL1', 'spondyloepimetaphyseal dysplasia with joint laxity, type 1, with or without fractures', 'SEMDJL']",0112198,271640,642099,,,,,,,,,
mondo:0010076,"spondyloepimetaphyseal dysplasia, Irapa type","['spondyloepimetaphyseal dysplasia, Irapa type', 'SEMDIT', 'SEMD, Irapa type']",,271650,93351,C0432213,,,,C562958,,,,
mondo:0010077,spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome,"['spondylometaepiphyseal dysplasia short limb-hand type', 'Smed, short limb-hand type', 'spondyloepimetaphyseal dysplasia - short limb - abnormal calcification', 'Smed short limb-abnormal calcification type', 'SMED type 2', 'SMED short limb-hand type', 'Smed-SL', 'spondylometaepiphyseal dysplasia, short limb-hand type', 'spondylometaepiphyseal dysplasia short limb-abnormal calcification type', 'spondylometaepiphyseal dysplasia, short limb-abnormal calcification type', 'Smed, type 2', 'Smed, short limb-abnormal calcification type', 'Smed-SL/Ac']",0112196,271665,93358,C1849011,"['-0.3923', '0.3682', '0.3372', '-0.593', '0.0693', '-0.2457', '0.1827', '0.521', '-0.6978', '0.03195', '-0.06934', '-0.01726', '-0.0954', '0.04767', '-0.2922', '0.1704', '0.237', '-0.08826', '-0.277', '-0.588', '-0.1226', '0.02007', '0.516', '-0.229', '-0.3027', '-0.07416', '-0.1576', '0.2043', '0.3694', '-0.227', '0.002314', '-0.02829', '0.2306', '-0.02928', '0.4758', '-0.2615', '0.2052', '-0.4236', '0.1522', '-0.6445', '0.1033', '-0.09503', '-0.1067', '0.05096', '-0.2231', '-0.1267', '-0.1439', '0.529', '0.1256', '0.0154', '-0.0853', '0.189', '0.1471', '0.0895', '-0.451', '-0.4858', '-0.3901', '-0.018', '0.199', '0.1467', '0.2312', '0.3057', '-0.7876', '0.152', '-0.3538', '-0.08057', '0.3132', '0.405', '-0.126', '0.2793', '-0.2659', '0.175', '0.2427', '-0.226', '-0.519', '0.1295', '0.2255', '0.04675', '-0.3176', '-0.282', '-0.1581', '-0.1126', '0.0754', '0.4263', '-0.224', '0.041', '0.047', '0.379', '0.3713', '0.0353', '-0.316', '-0.301', '-0.04483', '0.3318', '0.6987', '0.1349', '0.6665', '-0.1531', '0.3142', '0.1096']",,,C564794,,,,
mondo:0010078,spondyloperipheral dysplasia,"['spondyloperipheral dysplasia with short ulna', 'spondyloperipheral dysplasia', 'spondyloperipheral dysplasia-short ulna syndrome']",0112195,271700,1856,C0796173,,C135088,,C535799,758.89,,,
mondo:0010079,Canavan disease,"['Aspa deficiency', 'Von Bogaert-Bertrand disease', 'aspartoacylase deficiency', 'Acy2 deficiency', 'ACY2 deficiency', 'Canavan-Van Bogaert-Bertrand disease', 'Canavan-VAN Bogaert-Bertrand disease', 'spongy Degeneration of central nervous system', 'spongy degeneration of the brain', 'spongy degeneration of the central nervous system', 'spongy degeneration of central nervous system', 'aminoacylase 2 deficiency', 'Canavan disease', 'Asp deficiency']",3613,271900,141,C0206307,"['-0.2803', '0.322', '0.356', '-0.1433', '0.2242', '-0.4238', '-0.5923', '1.088', '-0.6987', '0.2074', '-0.428', '-0.3625', '-0.3938', '-0.1521', '0.356', '-0.3242', '-0.4321', '-0.1567', '-0.4954', '-0.3337', '-0.2344', '-0.4387', '0.6016', '-0.3645', '0.1014', '-0.1465', '0.067', '0.12445', '-0.4124', '-0.2678', '0.3804', '-0.0753', '-0.073', '0.253', '-0.1', '0.2463', '-0.695', '0.01566', '-0.2152', '-0.2837', '-0.2129', '-0.6104', '0.082', '-0.8813', '-0.2546', '0.22', '0.2742', '-0.03635', '-0.03137', '-0.286', '0.1208', '0.3481', '-0.2908', '-0.6714', '0.08105', '-0.3325', '0.1581', '-0.3284', '-0.01102', '0.0873', '-0.2479', '-0.4233', '0.3855', '0.1584', '0.08636', '-0.061', '-0.1764', '0.1902', '-0.825', '0.4133', '0.3203', '0.475', '-0.2393', '0.2808', '-0.1301', '0.3376', '0.1654', '0.1827', '-0.2505', '-0.2421', '-0.04605', '-0.757', '-0.5635', '0.917', '0.411', '-0.02425', '-0.2322', '-0.3762', '0.2905', '0.433', '0.444', '0.3347', '0.0443', '0.3027', '0.6084', '0.3635', '0.2913', '-0.0354', '0.1982', '-0.02144']",C84611,,D017825,,,10067608,
mondo:0010080,familial infantile bilateral striatal necrosis,"['striatal degeneration, familial', 'striatonigral degeneration, infantile', 'FBSN', 'bilateral striatal Necrosis, infantile', 'familial IBSN', 'familial infantile striatonigral necrosis', 'hereditary infantile bilateral striatal necrosis', 'familial bilateral striatal necrosis', 'familial infantile striatonigral degeneration', 'SNDI', 'infantile bilateral striatal necrosis']",,271930,225154,CN201303,"['-0.1414', '0.3875', '0.2908', '-0.119', '-0.1499', '-1.204', '0.3208', '0.3972', '-0.8027', '-0.473', '-0.062', '-0.4243', '-0.3987', '-0.5522', '0.3074', '-0.2935', '-0.2986', '-0.21', '0.489', '-1.1', '0.0745', '0.04663', '-0.05548', '-0.9346', '0.2087', '0.127', '0.1526', '-0.2986', '-0.9434', '0.229', '0.1821', '0.662', '0.3494', '0.02795', '0.09546', '0.553', '-0.3809', '-0.4146', '-0.9556', '-0.2676', '0.1774', '-0.5264', '0.2979', '-0.3816', '0.658', '-0.2262', '-0.566', '-0.1937', '-0.5464', '0.0708', '0.02106', '0.775', '-0.113', '-0.0395', '0.4502', '-0.2986', '0.648', '-0.296', '-0.8135', '0.5693', '0.0984', '-0.1982', '0.588', '-0.08014', '-0.623', '-0.678', '0.8955', '0.29', '-0.4602', '0.5864', '-0.1713', '0.007835', '-0.1893', '-0.249', '0.6064', '0.2622', '0.365', '0.2207', '0.01793', '-0.3364', '-0.1573', '0.1035', '-0.2927', '0.778', '0.5522', '0.03485', '-0.3196', '0.2416', '-0.05347', '-0.03345', '0.99', '0.1236', '0.1708', '0.1324', '0.1724', '0.1749', '0.77', '-0.2477', '0.06665', '-0.2876']",,,,,,,
mondo:0010081,"subaortic stenosis, membranous","['subaortic stenosis, membranous']",,271950,,,,,,C564793,,,,
mondo:0010082,subaortic stenosis-short stature syndrome,"['Onat syndrome', 'subaortic stenosis--short stature syndrome', 'subaortic stenosis short stature syndrome']",,271960,3191,C0795947,,,,C537749,,,,
mondo:0010083,succinic semialdehyde dehydrogenase deficiency,"['gamma-hydroxybutyricaciduria', 'SSADHD', 'gamma-hydroxybutyric aciduria', '4-hydroxybutyric aciduria', 'GABA metabolic defect', 'Ssadh deficiency', 'succinic semialdehyde dehydrogenase deficiency', 'SSADH', 'SSADH deficiency']",0060175,271980,22,C0268631,"['-0.233', '0.1534', '-0.5435', '0.1598', '-0.378', '-0.4204', '0.3', '0.8', '-0.595', '0.0841', '-0.3699', '-0.145', '0.00872', '0.1797', '0.2427', '0.0985', '-0.02983', '-0.386', '-0.305', '-0.5635', '-0.008644', '-0.0604', '0.3423', '-0.4797', '-0.09106', '-0.3667', '0.19', '-0.5527', '-0.253', '-0.2505', '0.0895', '-0.3171', '0.3682', '0.4207', '-0.2952', '-0.578', '-0.5244', '-0.1764', '-0.4658', '0.1016', '0.1825', '-0.5874', '-0.1553', '-0.03217', '0.4104', '0.08374', '-0.3557', '-0.0656', '-0.10754', '0.4817', '-0.1428', '0.735', '-0.5127', '-0.02786', '0.151', '0.3235', '0.03027', '-0.2861', '-0.3757', '0.509', '0.12195', '0.3079', '0.732', '-0.003092', '-0.557', '0.2375', '0.3948', '0.04892', '0.2107', '0.2361', '0.2225', '-0.2534', '-0.601', '0.1875', '0.216', '0.625', '0.3975', '-0.708', '-0.592', '-0.1617', '0.551', '-0.449', '-0.2778', '0.428', '0.5527', '0.797', '-0.3176', '0.318', '0.8965', '0.604', '0.5913', '0.343', '-0.2585', '-0.1855', '0.5293', '0.286', '0.3704', '-0.1267', '0.437', '-0.0003617']",,,C535803,,,,
mondo:0010084,"sucrosuria, hiatus hernia and intellectual disability","['sucrosuria, hiatus hernia and mental retardation', 'sucrosuria, hiatus hernia and intellectual disability']",,272000,,C1848963,,,,C564792,,,,
mondo:0010085,Schilder disease,"['Schilder disease', 'Myelinoclastic diffuse sclerosis', 'Schilder^s disease', 'SUDANOPHILIC cerebral sclerosis']",,272100,59298,C0007795,,,,,341.1,,,
mondo:0010087,Sugarman brachydactyly,"['Sugarman-Hager-Kulik syndrome', 'brachydactyly of the hands and feet with duplication of the first toes', 'Sugarman brachydactyly', 'brachydactyly with Major proximal phalangeal shortening', 'brachydactyly with major proximal phalangeal shortening']",0110979,272150,498602,,,,,,,,,
mondo:0010088,mucosulfatidosis,"['mucosulfatidosis', 'sulfatidosis juvenile, Austin type', 'MSD', 'juvenile sulfatidosis, Austin type', 'multiple sulfatase deficiency disease', 'sulfatidosis, juvenile, Austin type', 'multiple sulfatase deficiency', 'juvenile sulfatidosis']",0050441,272200,585,C0268263,"['-0.1582', '0.2808', '0.4382', '-0.01875', '0.01099', '-0.3389', '-0.03787', '-0.1121', '-0.3687', '-0.09143', '-0.2245', '0.0723', '-0.11426', '-0.264', '-0.02908', '-0.2302', '-0.1274', '-0.2433', '-0.564', '-0.4517', '0.0877', '-0.1543', '0.6255', '-0.04874', '0.075', '0.01952', '-0.1433', '-0.1256', '0.279', '0.0879', '0.3335', '0.2832', '0.626', '0.507', '0.2123', '-0.2615', '-0.4875', '-0.2062', '-0.215', '0.07587', '0.278', '-0.589', '0.12476', '0.337', '0.1405', '-0.4553', '0.04202', '0.1921', '-0.04965', '-0.01581', '-0.0655', '0.1534', '-0.03802', '-0.2478', '-0.00816', '-0.6606', '-0.188', '-0.2327', '-0.02031', '0.00378', '0.10486', '-0.1599', '0.1993', '0.2439', '0.11615', '-0.1409', '0.3064', '0.3813', '-0.3235', '0.2095', '-0.4683', '-0.1105', '-0.001916', '-0.1538', '-0.2625', '0.11115', '0.1621', '0.1172', '-0.2211', '-0.2393', '0.2666', '-0.4358', '-0.7734', '0.4204', '0.3015', '0.04764', '0.1448', '0.3035', '0.4932', '0.1418', '0.541', '0.592', '0.2297', '-0.02588', '0.4497', '0.4062', '0.3901', '-0.2451', '0.723', '-0.11957']",C84908,,D052517,,,,
mondo:0010089,isolated sulfite oxidase deficiency,"['sulfite oxidase deficiency', 'ISOD', 'sulfite oxidase deficiency, isolated', 'Sulfocysteinuria', 'sulfocysteinuria']",0111270,272300,99731,,"['-0.2515', '0.142', '-0.012344', '-0.01396', '0.0861', '-0.0987', '-0.014534', '0.1714', '-0.04355', '-0.005085', '-0.04306', '-0.0692', '-0.032', '-0.03836', '-0.01903', '0.006054', '0.04913', '0.0642', '-0.2234', '-0.3882', '-0.0693', '-0.1743', '0.1792', '-0.05966', '0.0503', '0.01282', '-0.02885', '-0.05237', '-0.0283', '-0.1106', '0.1685', '0.1126', '0.1868', '0.1525', '0.01067', '-0.1575', '0.08936', '-0.1398', '0.05618', '-0.2686', '0.000478', '-0.2585', '0.0787', '-0.1647', '-0.1765', '-0.2123', '0.07806', '0.0635', '0.02454', '0.1251', '-0.04257', '-0.0983', '0.00929', '-0.04608', '-0.2018', '-0.006645', '0.2476', '-0.105', '-0.2668', '0.08215', '0.127', '0.0587', '0.06143', '-0.1095', '0.00438', '0.01736', '0.2283', '0.03256', '-0.2659', '0.1117', '-0.1072', '-0.02838', '-0.07965', '-0.1478', '0.1094', '0.1416', '0.109', '-0.03001', '-0.03693', '0.0488', '0.02242', '0.0646', '-0.04703', '0.1445', '0.0907', '0.003525', '0.01752', '0.161', '0.2869', '-0.00471', '0.1622', '0.07495', '-0.1285', '-0.0808', '0.3577', '0.2308', '0.1665', '-0.2979', '-0.0858', '0.04236']",,,C538141,,,,
mondo:0010090,Summitt syndrome,"['Summitt syndrome', 'recessive acrocephalosyndactyly with normal intelligence', 'Summitt^s acrocephalosyndactyly']",,272350,3210,C1802405,,,,C538142,,Q82.0,,
mondo:0010091,Cold-induced sweating syndrome 1,"['Crisponi/cold-induced sweating syndrome 1', 'Sohar-Crisponi syndrome', 'CISS1', 'cold-induced sweating syndrome type 1', 'Crisponi syndrome', 'muscle contractions, Tetanoform, with characteristic face, camptodactyly, hyperthermia, and sudden death', 'cold-induced sweating syndrome 1', 'CRISPONI/cold-induced sweating syndrome 1']",0080329,601378,1545,,"['0.2983', '0.263', '-0.69', '-0.5845', '-0.1395', '-0.477', '-0.04752', '0.9336', '-0.3928', '-0.5527', '0.02522', '0.1381', '-0.02357', '-0.308', '-0.3806', '0.8765', '0.6265', '-0.1648', '0.0768', '-0.645', '0.0665', '0.187', '0.08984', '-0.4685', '-0.3984', '-0.4673', '0.09924', '-0.00807', '-0.04706', '-0.3127', '0.9077', '0.04172', '0.544', '0.5396', '-0.4426', '0.486', '0.4705', '-0.4504', '-0.2349', '-0.0836', '-0.01322', '-0.1908', '-0.082', '0.2874', '0.1648', '0.436', '-0.2079', '0.2197', '-0.297', '1.22', '-0.64', '-0.197', '-0.1307', '-0.02403', '0.3552', '-0.1293', '0.4158', '0.2988', '0.5137', '0.1552', '0.09875', '0.5854', '-0.004883', '-0.006283', '-0.02321', '-0.2615', '0.699', '0.275', '-0.784', '0.644', '-0.4321', '0.02257', '0.1062', '0.6562', '0.2258', '-0.0826', '0.1703', '-0.10376', '0.03558', '0.72', '0.0205', '-0.2146', '0.4563', '0.3223', '-0.3535', '0.3552', '0.0631', '0.6504', '0.635', '-0.292', '-0.3684', '-0.1583', '0.4873', '0.152', '0.495', '0.2367', '0.08453', '-0.479', '0.2783', '-0.002169']",,,C536214,,,,
mondo:0010092,Filippi syndrome,"['unusual facial appearance, microcephaly, growth and intellectual disability and syndactyly', 'syndactyly, type I, with microcephaly and intellectual disability', 'Scott craniodigital syndrome with mental retardation', 'syndactyly type I with microcephaly and intellectual disability', 'FILIPPI syndrome', 'syndactyly type I with microcephaly and mental retardation', 'syndactyly, type I, with microcephaly and mental retardation', 'Filippi syndrome', 'type 1 syndactyly-microcephaly-intellectual disability syndrome', 'FLPIS', 'Scott craniodigital syndrome with intellectual disability', 'unusual facial appearance, microcephaly, growth and mental retardation and syndactyly']",0112194,272440,3255,C0795940,"['-0.03116', '0.075', '0.1588', '-0.5645', '0.1654', '-0.1719', '-0.0502', '0.72', '-0.3755', '-0.3645', '-0.1346', '-0.0431', '0.010574', '-0.2603', '-0.371', '0.2725', '0.6714', '-0.135', '-0.15', '-0.4536', '0.1089', '0.0614', '-0.003233', '-0.01892', '0.264', '-0.02716', '-0.3142', '0.04587', '0.563', '-0.5337', '0.4465', '-0.4268', '0.4048', '0.2498', '0.2515', '-0.03366', '-0.0755', '-0.2094', '0.0338', '-0.3809', '0.0483', '-0.1567', '-0.09717', '-0.3264', '-0.08044', '-0.3186', '0.0927', '0.4043', '-0.2598', '-0.3972', '-0.1931', '-0.07104', '-0.2869', '0.12427', '-0.5254', '-0.1881', '0.02406', '-0.2249', '-0.08203', '0.09106', '0.06433', '0.1349', '-0.3196', '0.05347', '0.0825', '-0.1069', '-0.02844', '0.39', '-0.508', '0.34', '-0.5', '0.4917', '0.1957', '-0.12286', '-0.01077', '0.1581', '0.03903', '-0.4082', '-0.11005', '-0.01505', '0.177', '0.1042', '0.362', '0.6704', '0.05762', '0.3025', '-0.254', '0.4534', '0.02362', '0.502', '0.05557', '0.322', '0.308', '0.2413', '0.8125', '0.1038', '0.3247', '-0.6553', '0.309', '0.3262']",,,C538152,,,,
mondo:0010093,syndesmodysplasic dwarfism,['syndesmodysplasic dwarfism'],,272450,2654,C2931647,,,,C537869,,,,
mondo:0010094,spondylocarpotarsal synostosis syndrome,"['spondylocarpotarsal synostosis syndrome', 'vertebral fusion with carpal coalition', 'Synspondylism', 'congenital synspondylism', 'Synspondylism congenital', 'Synspondylism, congenital', 'scoliosis, congenital with unilateral unsegmented bar', 'scoliosis, congenital, with unilateral unsegmented Bar', 'spondylocarpotarsal synostosis', 'SCT', 'congenital scoliosis with unilateral unsegmented bar', 'spondylocarpotarsal syndrome']",0090116,272460,3275,C1848934,"['-0.5444', '-0.16', '0.077', '-0.08545', '0.366', '-0.342', '0.333', '0.795', '-0.3794', '-0.553', '-0.4377', '0.0899', '-0.419', '0.457', '-0.1434', '0.0855', '0.268', '-0.409', '-0.742', '-0.2876', '-0.1555', '0.3672', '0.3208', '-0.1997', '-0.3254', '-0.2983', '-0.2023', '0.1348', '0.36', '-0.1896', '-0.2239', '-0.3394', '0.0683', '0.1008', '-0.0204', '-0.2754', '0.0397', '-0.64', '-0.009056', '0.0383', '-0.2468', '-0.0806', '0.7983', '-0.2064', '0.4656', '0.1476', '-0.7656', '0.2961', '-0.229', '-0.1863', '0.3635', '-0.2241', '0.2384', '0.004818', '0.1146', '-0.7666', '-0.4524', '-0.2964', '0.609', '0.1338', '0.04395', '0.3318', '-0.6694', '-0.03632', '-0.598', '0.07635', '0.04926', '1.0625', '0.0544', '0.3577', '-0.256', '0.2285', '0.0639', '-0.2224', '-0.4114', '0.0966', '-0.2688', '0.00924', '-0.3806', '-0.3013', '0.005497', '0.12445', '-0.4292', '1.008', '0.2052', '0.7876', '0.251', '0.1769', '0.836', '-0.0755', '0.08844', '0.372', '-0.4941', '0.4116', '1.044', '-0.2932', '0.5117', '-0.4043', '0.787', '0.0952']",,,C535780,758.89,,,
mondo:0010095,ataxia-tapetoretinal degeneration syndrome,['tapetoretinal degeneration with ataxia'],,272600,1178,C1848932,,,,C564788,,,,
mondo:0010096,tardive dyskinesia,"['tardive dyskinesia', 'tardive dyskinesia (disease)']",,272620,,C0686347,,,,D000071057,,,,0040141
mondo:0010097,Tatsumi factor deficiency,['Tatsumi factor deficiency'],,272650,,C1848931,,,,C564787,,,,
mondo:0010098,taurodontism,"['taurodontism (disease)', 'Bull teeth', 'large pulp chambers in the molars', 'taurodontism']",,272700,3289,C0266039,,,,C536946,,,,0000679
mondo:0010099,Tay-Sachs disease AB variant,"['Tay-Sachs disease, AB variant', 'hexosaminidase activator deficiency', 'Tay-Sachs disease, variant AB', 'Ab variant GM2-gangliosidosis', 'GM2 gangliosidosis, AB variant', 'GM2 activator deficiency', 'GM2-gangliosidosis, AB variant']",4795,272750,309246,C0268275,"['0.00923', '0.5117', '0.5283', '0.205', '0.2485', '-0.02568', '-0.6416', '0.564', '-0.4019', '-0.1345', '0.1268', '0.3933', '-0.402', '0.1608', '0.385', '-0.6694', '-0.1153', '0.06464', '-0.5596', '-0.4897', '-0.5903', '-0.563', '-0.2913', '-0.04352', '-0.3691', '-0.2935', '-0.1885', '0.0988', '-0.571', '-0.7417', '0.2109', '0.3257', '0.6655', '-0.4321', '-0.488', '0.434', '-0.5513', '-0.71', '-0.47', '-0.5923', '0.2036', '0.04153', '-0.013885', '-0.247', '-0.0715', '-0.06024', '0.01545', '-0.1337', '-0.08655', '0.4614', '-0.1231', '-0.09863', '-0.3196', '-0.318', '0.3745', '-0.969', '0.1313', '0.346', '-0.1862', '-0.2776', '-0.1288', '-0.3032', '0.3555', '0.4534', '0.0669', '0.653', '0.517', '-0.2617', '-0.89', '-0.3435', '-0.454', '0.2969', '0.0598', '-0.3032', '0.04935', '0.279', '0.2996', '0.4602', '-0.2482', '-0.319', '0.495', '-1.013', '-0.8745', '0.1504', '0.8115', '-0.3362', '0.3057', '0.4382', '0.4836', '0.0607', '0.119', '0.4648', '-0.094', '0.2012', '0.4995', '0.1638', '-0.1876', '-0.2207', '0.3813', '-0.3457']",C133084,,D049290,,,,
mondo:0010100,Tay-Sachs disease,"['hexosaminidase alpha-subunit deficiency (variant B)', 'Tay-Sachs disease, juvenile', 'GM2 gangliosidosis, B, B1 variant', 'Tay-Sachs disease, variant B1', 'B variant GM2 gangliosidosis', 'gangliosidosis GM2, type 1', 'B variant GM2-gangliosidosis', 'GM2-gangliosidosis, adult chronic type', 'disease, Tay-Sachs', 'Tay-Sachs disease', 'GM2-gangliosidosis, type 1', 'hexosaminidase A deficiency', 'Hex A pseudodeficiency', 'hexa deficiency', 'TSD', 'hexosaminidase a deficiency', 'TAY-Sachs disease', 'GM2 gangliosidosis, type 1', 'GM2-gangliosidosis, several forms', 'GM2-gangliosidosis, variant B1', 'Tay-Sachs disease, pseudo-Ab variant', 'hexosaminidase a deficiency, adult type', 'sphingolipidosis, Tay-Sachs']",3320,272800,845,C0039373,"['-0.2268', '0.9736', '-0.08984', '0.57', '0.1475', '-0.491', '-0.4282', '0.6724', '-0.841', '-0.259', '-0.1039', '0.3176', '-0.4866', '0.284', '0.501', '-0.4773', '-0.2727', '0.02438', '-0.3738', '-0.1921', '-0.1211', '-0.4204', '-0.0041', '-0.01189', '-0.5957', '-0.554', '0.1973', '0.01265', '-0.4192', '-0.4211', '0.6797', '0.285', '0.3157', '0.1346', '-0.552', '0.0813', '-0.4524', '-0.4573', '-0.1792', '-0.208', '-0.05927', '-0.2207', '-0.1957', '-0.0173', '0.1934', '0.3198', '-0.2117', '-0.2003', '-0.227', '0.435', '0.4443', '-0.11127', '-0.1106', '-0.3936', '0.0702', '-0.565', '0.0609', '-0.02939', '-0.2834', '0.05234', '-0.286', '-0.3398', '0.1478', '0.2322', '0.03244', '0.4353', '0.3218', '-0.2444', '-0.6514', '-0.03394', '0.06683', '-0.0992', '-0.12085', '-0.2795', '0.10016', '0.3113', '0.12146', '0.1127', '-0.356', '-0.0386', '0.3997', '-0.9536', '-0.544', '-0.1685', '0.03598', '-0.271', '0.1421', '0.5317', '0.497', '0.3923', '0.1268', '0.3252', '-0.581', '0.1184', '-0.004467', '0.2769', '-0.237', '-0.329', '0.007767', '-0.4297']",C85184,,D013661,,E75.02,10043147,
mondo:0010101,Teebi-Shaltout syndrome,"['TBSH', 'craniofacial anomalies, abnormal hair, camptodactyly, and caudal appendage', 'Teebi Shaltout syndrome', 'Teebi-Shaltout syndrome']",,272950,3291,C1848912,,,,C536950,,,,
mondo:0010102,taurodontia-absent teeth-sparse hair syndrome,"['taurodontia, absent teeth, and sparse hair', 'taurodontia, absent teeth, sparse hair syndrome', 'teeth, congenital absence of, with taurodontia and sparse hair']",,272980,2731,C1848909,,,,C536945,,,,
mondo:0010103,"teeth, fused","['teeth, fused']",,273000,,,,,,D005671,,,,
mondo:0010104,non-eruption of teeth-maxillary hypoplasia-genu valgum syndrome,"['non erupted teeth with maxillary hypoplasia and genu valgum', 'Stoelinga de Koomen Davis syndrome', 'Stoelinga-de Koomen-Davis syndrome', 'multiple non-erupting teeth, maxillo-zygomatical hypoplasia and other congenital defects', 'teeth noneruption of with maxillary hypoplasia and genu valgum', 'teeth, noneruption of, with maxillary hypoplasia and genu valgum', 'multiple none-erupting teeth, maxillo-zygomatical hypoplasia and other congenital defects']",,273050,2972,C1848903,,,,,,,,
mondo:0010105,"teratoma, pineal","['teratoma, pineal']",,273120,,C1848902,,,,C537401,,,,
mondo:0010106,"testes, rudimentary","['testes, rudimentary']",,273150,,,,,,,,,,
mondo:0010108,testicular germ cell tumor,"['testicular germ cell cancer', 'testis germ cell tumour', 'Male germ cell tumor', 'testicular germ cell tumor', 'germ cell tumor of testis', 'germ cell tumor of the testis', 'testicular tumor, somatic', 'endodermal sinus tumor', 'nonseminomatous germ cell tumours', 'endodermal sinus tumour', 'spermatocytic seminoma, somatic', 'germ cell tumour of testis', 'testis germ cell tumor', 'seminoma', 'testicular germ cell neoplasm', 'germ cell tumour of the testis', 'nonseminomatous germ cell tumors', 'germ cell neoplasm of the testis', 'male germ cell tumor, somatic', 'teratoma, testicular', 'spermatocytic seminoma', 'TGCT', 'germ cell neoplasm of testis', 'embryonal cell carcinoma', 'Male germ cell tumour', 'testicular germ cell neoplasms', 'germ cell tumors, somatic']",5557,273300,876,C1336708,"['-0.1676', '0.11237', '0.007195', '-0.1528', '0.1533', '-0.1168', '0.1576', '0.01204', '-0.0635', '-0.07684', '0.05588', '0.03302', '-0.0922', '0.11774', '-0.2205', '-0.1615', '-0.0815', '-0.2457', '0.05542', '-0.246', '-0.1418', '-0.329', '0.2029', '-0.2532', '0.1726', '-0.2125', '0.04132', '-0.0626', '-0.1346', '-0.2505', '0.3015', '0.002342', '0.3945', '-0.1656', '-0.06903', '-0.0417', '-0.1356', '0.132', '-0.0327', '-0.2788', '0.005337', '-0.08484', '0.03967', '-0.1656', '0.1179', '-0.1472', '0.0385', '-0.01517', '0.1646', '0.1476', '0.01188', '-0.03357', '-0.097', '0.2024', '-0.2808', '0.1296', '0.1687', '0.03506', '-0.3467', '0.07587', '0.2563', '-0.01475', '-0.1714', '0.2239', '0.02057', '0.10785', '0.3538', '0.3262', '-0.1353', '0.3118', '-0.1089', '0.1815', '0.0596', '0.026', '0.0862', '0.02663', '-0.05734', '0.03108', '-0.0979', '-0.3186', '-0.2773', '0.0809', '-0.1383', '0.05298', '-0.2964', '-0.1642', '0.1617', '-0.02383', '0.2632', '-0.1849', '-0.06058', '0.2042', '-0.0281', '-0.1093', '0.3806', '-0.09705', '0.1898', '-0.1919', '-0.1737', '0.06854']",C8591,1000566,C563236,239.5,,,
mondo:0010109,tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities,"['tetra-amelia, ectodermal dysplasia, and lacrimal duct abnormality', 'tetraamelia with ectodermal dysplasia and lacrimal duct abnormalities', 'Madokoro Ohdo Sonoda syndrome']",,273390,,,,,,C536496,,,,
mondo:0010110,tetraamelia-multiple malformations syndrome,"['TETRAAMELIA syndrome, autosomal recessive', 'Zimmer phocomelia', 'TETAMS', 'Tetraamelia multiple malformations X-linked', 'Zimmer Taub Sova syndrome']",0112191,,3301,C2931218,"['0.1866', '-0.10455', '-0.11774', '-0.5303', '0.241', '-0.0914', '0.1604', '0.7397', '-0.512', '-0.3853', '0.0909', '-0.2856', '-0.305', '-0.0464', '-0.287', '0.1439', '0.1682', '-0.0248', '-0.635', '-0.0874', '-0.2346', '0.05273', '0.698', '-0.753', '-0.1497', '-0.02693', '-0.1768', '-0.03915', '0.2524', '-0.01831', '0.514', '-0.2527', '0.1602', '-0.1803', '0.1743', '0.02126', '-0.275', '-0.3748', '-0.2435', '-0.1348', '-0.0704', '-0.2183', '-0.1545', '-0.5327', '0.4534', '-0.1967', '0.12366', '0.3535', '-0.7725', '0.015594', '-0.4355', '0.0788', '0.189', '-0.1262', '-0.8535', '-0.3274', '0.0993', '0.2742', '0.1609', '-0.4143', '-0.04587', '0.038', '0.203', '0.1584', '-0.6396', '-0.1355', '0.1958', '0.6147', '-0.9824', '0.2051', '-0.1542', '0.2307', '-0.01569', '0.2524', '-0.09656', '0.2043', '-0.2261', '0.3506', '-0.2166', '-0.3315', '-0.2498', '-0.3325', '0.2135', '0.4963', '-0.04498', '-0.4329', '0.3884', '0.2832', '-0.1343', '-0.542', '0.307', '0.2754', '0.1648', '0.077', '0.9263', '0.2367', '0.4148', '-0.844', '0.125', '0.0824']",,,C536500,,,,
mondo:0010111,odontotrichomelic syndrome,"['tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities', 'odontotrichomelic hypohidrotic dysplasia', 'Freire-Maia syndrome', 'Freire-Maia odontotrichomelic syndrome', 'odontotrichomelic syndrome']",,273400,2723,CN074199,,,,C535637,,,,
mondo:0010112,"thalamic degeneration, symmetric infantile","['symmetric infantile thalamic degeneration', 'symmetrical thalamic degeneration in infants', 'thalamic degeneration, symmetric infantile']",,273490,3311,C2931220,,,,C536504,,,,
mondo:0010114,"thanatophoric dysplasia, Glasgow variant","['thanatophoric dysplasia, Glasgow variant', 'neonatally lethal short-limb skeletal dysplasia, Glasgow type']",,273680,93275,C1848865,,,,C536506,,,,
mondo:0010115,thoracic dysplasia-hydrocephalus syndrome,"['thoracic dysplasia-hydrocephalus syndrome', 'thoracic dysplasia hydrocephalus syndrome']",,273730,1861,C1848864,,,,C564774,,,,
mondo:0010116,thoracomelic dysplasia,"['^thoraco-limb^ dysplasia', 'thoraco-limb dysplasia', 'Rivera-Perez-Salas syndrome', 'thoracolimb dysplasia, Rivera type', 'thoracomelic dysplasia']",,273740,1803,C1848863,,,,C564773,,,,
mondo:0010117,3M syndrome 1,"['three M syndrome type 1', 'CUL7 3-M syndrome', '3M1', 'Le Merrer syndrome', 'Yakut short stature syndrome', 'Dolichospondylic dysplasia', 'gloomy face syndrome', '3M syndrome', '3-M syndrome 1', '3-M syndrome caused by mutation in Cul7', 'Cul7 3-M syndrome', 'three M syndrome 1']",,273750,,,,,,,,,,
mondo:0010118,inherited threoninemia,"['hyperthreoninemia', 'threoninemia']",,273770,,,,,,,,,,
mondo:0010120,thrombocytopenia 3,"['thrombocytopenia 3', 'THC3', 'thrombocytopenia, autosomal recessive, 3']",,273900,,C2678311,,,,C567487,,,,
mondo:0010121,thrombocytopenia-absent radius syndrome,"['TAR', 'TAR syndrome', 'thrombocytopenia absent radii', 'thrombocytopenia absent radius syndrome', 'thrombocytopenia with absent radii (TAR) syndrome', 'Tar syndrome', 'radial aplasia-thrombocytopenia syndrome', '1q21.1 susceptibility locus for Thrombocytopenia-Absent Radius (TAR) syndrome', 'absent radii and thrombocytopenia', 'thrombocytopenia-absent radius syndrome', 'chromosome 1Q21.1 deletion syndrome, 200-Kb']",14699,274000,3320,C0175703,"['-0.06122', '-0.3862', '0.0939', '-0.317', '0.2983', '0.2102', '0.0388', '0.7886', '-0.653', '-0.611', '-0.1114', '-0.1752', '0.1604', '0.3171', '-0.3352', '-0.03653', '-0.1875', '0.2181', '-0.1052', '-0.529', '-0.1305', '0.006775', '0.2952', '-0.4333', '0.239', '-0.0715', '-0.0824', '0.00735', '0.5293', '-0.038', '0.452', '-0.3572', '-0.05716', '0.6733', '-0.0746', '-0.04987', '-0.2698', '0.02335', '-0.2769', '0.0402', '-0.0742', '0.302', '0.1536', '-0.408', '0.00921', '0.11536', '-0.376', '0.614', '-0.2279', '0.1425', '-0.535', '-0.03772', '0.2483', '0.05927', '-0.613', '0.082', '0.2407', '-0.1572', '-0.2484', '0.04062', '0.11694', '0.2385', '0.1169', '-0.3044', '-0.1354', '-0.3718', '0.287', '0.349', '-0.3843', '0.3748', '0.0873', '0.2778', '-0.553', '-0.10846', '0.656', '0.02278', '0.463', '-0.912', '-0.64', '-0.1294', '-0.2229', '-0.6177', '0.2079', '0.3032', '-0.2964', '0.1353', '0.03177', '0.03748', '-0.236', '-0.6245', '-0.04312', '0.0921', '-0.006523', '-0.2152', '0.3848', '0.04675', '0.9414', '-0.5977', '0.2224', '0.07043']",C99038,,C536940,759.89,,10071719,
mondo:0010122,congenital thrombotic thrombocytopenic purpura,"['Microangiopathic hemolytic Anemia, congenital', 'congenital ADAMTS-13 deficiency', 'thrombotic thrombocytopenic purpura, hereditary', 'TTP', 'Upshaw Factor, deficiency of', 'thrombotic microangiopathy, familial', 'Microangiopathic hemolytic Anemia', 'TTP, congenital', 'thrombotic thrombocytopenic purpura, congenital', 'Schulman-Upshaw syndrome', 'congenital TTP', 'USS', 'thrombotic thrombocytopenic purpura, familial', 'Microangiopathic hemolytic Anaemia', 'hereditary thrombotic thrombocytopenic purpura', 'Upshaw-Schulman syndrome', 'familial TTP', 'congenital ADAMTS13 deficiency']",,274150,93583,,"['-0.0126', '0.0868', '-0.0702', '-0.02432', '0.0538', '-0.02866', '-0.02448', '0.0679', '-0.03714', '-0.04123', '-0.007195', '0.03058', '0.03333', '-0.0318', '-0.1', '-0.09607', '-0.1037', '-0.03833', '-0.02026', '-0.2021', '0.02121', '-0.0484', '0.1396', '-0.0616', '-0.01035', '-0.03123', '-0.02368', '-0.04364', '0.0695', '-0.0869', '0.08307', '0.0416', '0.191', '0.0942', '0.0182', '-0.0639', '-0.0739', '-0.08185', '-0.03546', '-0.09143', '0.014694', '-0.0993', '0.08734', '-0.0664', '0.01315', '-0.05356', '-0.04022', '0.1104', '0.0191', '0.0792', '-0.01619', '0.007557', '0.04898', '0.04016', '-0.11584', '-0.01255', '0.12445', '-0.0809', '-0.1777', '0.010254', '0.11664', '0.05573', '0.012', '-0.02072', '0.10614', '-0.02106', '0.1671', '0.1282', '-0.1329', '0.1481', '-0.07825', '-0.0349', '-0.0278', '-0.0904', '0.05527', '0.01846', '0.0897', '-0.02083', '-0.003277', '-0.03076', '-0.05795', '-0.03278', '-0.03867', '0.06366', '-0.00421', '-0.02249', '0.0909', '0.10004', '0.0669', '-0.0597', '0.1558', '0.0609', '0.05624', '0.000561', '0.2104', '0.0964', '0.1393', '-0.1461', '-0.05856', '-0.01036']",C131657,,,287.33,M31.3,,
mondo:0010123,absent thumb-short stature-immunodeficiency syndrome,"['thumb agenesis, short stature, and immunodeficiency']",,274190,2951,C1848818,,,,C564770,,,,
mondo:0010124,"thumb, distal hyperextensibility of","['thumb, distal hyperextensibility of']",,274200,,,,,,,,,,
mondo:0010125,upper limb defect-eye and ear abnormalities syndrome,"['thumb, hypoplastic, with choroid coloboma, poorly developed antihelix, and deafness']",,274205,2489,C1848816,,,,C564769,,,,
mondo:0010126,thymic aplasia with fetal death,['thymic aplasia with fetal death'],,274210,,C1848815,,,,C564768,,,,
mondo:0010127,"thymoma, familial","['hereditary thymoma (disease)', 'thymoma, familial', 'thymic neoplasia']",,274230,,C1848814,,,,C564767,,,,
mondo:0010128,thyrocerebrorenal syndrome,"['THYROCEREBRORETINAL syndrome', 'Thyrocerebral-retinal syndrome', 'cutler-Bass-Romshe syndrome']",,274240,3327,C4518579,,,,C536908,,,,
mondo:0010129,thymic-renal-anal-lung dysplasia,"['thymic-renal-anal-lung dysplasia', 'syndrome of unilobed or absent thymus, renal and ureter agenesis/dysgenesis, and intrauterine growth retardation (IUGR)']",,274265,3326,C1848812,,,,C536907,,,,
mondo:0010130,dihydropyrimidine dehydrogenase deficiency,"['thymine-uracilurea', 'dihydrouracil dehydrogenase deficiency', 'DPD deficiency', 'hereditary thymine-uraciluria', 'DYPD deficiency', 'thymine-Uraciluria, hereditary', 'pyrimidinemia, familial', 'familial pyrimidinemia', 'Dpyd deficiency', 'familial pyrimidinaemia', 'dihydropyrimidine dehydrogenase deficiency']",14218,274270,1675,C1959620,"['-0.3455', '0.094', '-0.3582', '-0.4573', '-0.1857', '-0.1643', '-0.03793', '-0.04465', '-0.2842', '0.10724', '0.0496', '0.2009', '0.1981', '0.0859', '-0.1328', '0.11334', '-0.04993', '-0.172', '-0.558', '-0.5664', '-0.1965', '0.1669', '0.357', '-0.412', '0.3662', '-0.2405', '-0.08484', '0.2327', '-0.396', '-0.1692', '0.3047', '-0.0408', '0.3982', '0.4043', '-0.054', '-0.08966', '-0.1428', '-0.4673', '-0.02083', '-0.10455', '0.06494', '-0.4263', '-0.2316', '-0.106', '-0.1857', '-0.3896', '0.6675', '-0.1097', '0.1833', '0.6147', '-0.3193', '-0.567', '-0.3118', '-0.1378', '0.1952', '0.2195', '0.05927', '0.035', '-0.277', '0.459', '0.0225', '-0.08295', '0.4282', '0.326', '-0.4504', '0.453', '0.3423', '0.2183', '-0.2815', '-0.0829', '-0.1247', '0.366', '-0.3213', '-0.05557', '0.1396', '0.2489', '0.5674', '-0.6064', '0.403', '-0.04996', '0.01224', '0.1142', '0.00569', '0.2944', '-0.134', '-0.139', '-0.3784', '0.2776', '0.4927', '0.649', '0.424', '0.328', '-0.2429', '0.05292', '0.404', '0.6416', '-0.122', '-0.02187', '0.0639', '0.0395']",C84672,,D054067,277.2,,10052622,
mondo:0010131,"thyroid hormone resistance, generalized, autosomal recessive","['thyroid hormone resistance, autosomal recessive', 'thyroid hormone resistance, generalized, autosomal recessive', 'GRTH', 'thyroid hormone resistance', 'THRB', 'Gthr', 'thyroid hormone resistance syndrome', 'Refetoff syndrome', 'thyroid hormone receptor BETA', 'thyroid hormone unresponsiveness']",,274300,,,,C85191,,C567936,,,,
mondo:0010132,familial thyroid dyshormonogenesis,"['dyshormonogenesis', 'nongoitrous hyperthyrotropinemia', 'thyroid dyshormonogenesis']",0112183,,95716,C1848805,"['-0.1958', '0.5967', '-0.4043', '0.3796', '0.6943', '0.4893', '0.328', '0.519', '-0.4822', '-0.4072', '-0.0767', '0.1417', '0.1704', '0.4802', '-0.108', '-0.5444', '-0.5146', '-0.3376', '0.02539', '-0.7183', '0.01996', '-0.1794', '0.486', '-0.6895', '0.5483', '0.3', '-0.1242', '0.1654', '0.003422', '-0.282', '0.2054', '1.007', '0.225', '0.6245', '-0.7803', '-0.10406', '-0.1132', '-0.1104', '-0.731', '0.2974', '0.5054', '-0.1884', '0.479', '-0.1465', '-0.217', '-0.02528', '0.3213', '0.005264', '-0.2316', '0.2715', '-0.295', '-0.2715', '-0.313', '-0.7817', '-0.51', '-0.1786', '0.4385', '-0.4187', '-0.501', '0.2825', '0.4263', '0.02545', '0.1219', '-0.3486', '0.1356', '0.4868', '0.7783', '-0.0696', '-0.6416', '-0.459', '0.2915', '0.9077', '0.3599', '-0.8135', '0.5684', '-0.3313', '-0.3628', '-0.2842', '-0.638', '-0.0223', '-0.314', '0.3164', '-0.514', '-0.383', '0.03775', '0.01249', '0.6294', '-0.0441', '0.7983', '-0.001392', '0.563', '0.4102', '-0.562', '-0.2617', '0.558', '0.1106', '0.01466', '-0.4556', '-0.02748', '0.751']",C121751,,C564766,,,,
mondo:0010133,thyroid dyshormonogenesis 2A,"['hypothyroidism, congenital, due to dyshormonogenesis, 2A', 'thyroid dyshormonogenesis type 2A', 'thyroid hormonogenesis, genetic defect in, 2A', 'thyroid dyshormonogenesis 2A', 'thyroid peroxidase deficiency', 'iodide peroxidase deficiency', 'familial thyroid dyshormonogenesis caused by mutation in TPO', 'TDH2A', 'TPO familial thyroid dyshormonogenesis']",0112186,274500,,C1291299,,C121750,,C563206,277.6,,,
mondo:0010134,Pendred syndrome,"['deafness with goitre', 'hypothyroidism, congenital, due to dyshormonogenesis, 2B', 'genetic defect in thyroid hormonogenesis 2B', 'autosomal recessive sensorineural hearing impairment and goiter', 'congenital hypothyroidism due to dyshormonogenesis 2B', 'thyroid hormonogenesis, genetic defect in, 2B', 'deafness with goiter', 'TDH2B', 'thyroid dyshormonogenesis 2B', 'Pendred syndrome', 'PDS', 'autosomal recessive sensorineural hearing impairment and goitre', 'goiter-deafness syndrome']",0060744,274600,705,C0271829,"['0.10504', '0.3633', '-0.085', '0.33', '0.1655', '0.02483', '0.3508', '0.9297', '-0.3684', '-0.683', '0.2076', '-0.648', '-0.2151', '0.4219', '0.1716', '-0.615', '-0.716', '-0.626', '-0.529', '-0.5913', '0.2578', '-0.0165', '0.3457', '0.1813', '0.8643', '0.602', '-0.2546', '-0.06024', '0.01953', '-0.2954', '0.2944', '0.4084', '-0.3086', '1.044', '-0.215', '0.02782', '-0.1205', '0.1169', '-0.1854', '-0.3518', '0.1876', '0.4307', '0.7905', '-0.4973', '-0.02266', '-0.559', '0.2415', '-0.7896', '0.1775', '0.5986', '0.000661', '0.11053', '-0.06604', '-0.5405', '-0.05008', '-0.3293', '0.878', '-0.3167', '-0.1841', '-0.05716', '0.3503', '-0.1842', '0.1555', '0.1613', '-0.197', '0.003643', '-0.2612', '0.171', '-0.2566', '0.083', '-0.3389', '0.1123', '-0.2245', '-0.0345', '0.8584', '-0.3794', '0.838', '0.4116', '-0.679', '0.0544', '0.1901', '-0.09656', '-0.5146', '0.3267', '-0.06042', '0.0486', '-0.05667', '-0.301', '-0.3284', '0.3616', '0.518', '0.545', '-0.2056', '-0.0785', '0.9014', '-0.5127', '0.4368', '-0.489', '0.10486', '-0.0462']",C121745,,C536648,,,,
mondo:0010135,thyroid dyshormonogenesis 3,"['TG familial thyroid dyshormonogenesis', 'TDH3', 'thyroid hormonogenesis, genetic defect in, 3', 'hypothyroidism, congenital, due to dyshormonogenesis, 3', 'thyroid dyshormonogenesis 3', 'thyroid dyshormonogenesis type 3', 'familial thyroid dyshormonogenesis caused by mutation in TG']",0112187,274700,,C0342194,,,,C562769,,,,
mondo:0010136,thyroid dyshormonogenesis 4,"['thyroid dyshormonogenesis type 4', 'deiodinase deficiency', 'IYD familial thyroid dyshormonogenesis', 'iodotyrosine dehalogenase deficiency', 'thyroid dyshormonogenesis 4', 'familial thyroid dyshormonogenesis caused by mutation in IYD', 'thyroid hormonogenesis, genetic defect in, 4', 'hypothyroidism, congenital, due to dyshormonogenesis, 4', 'TDH4']",0112188,274800,,C0342195,,,,C562770,,,,
mondo:0010137,thyroid dyshormonogenesis 5,"['thyroid dyshormonogenesis 5', 'DUOXA2 familial thyroid dyshormonogenesis', 'thyroid dyshormonogenesis type 5', 'thyroid hormonogenesis, genetic defect in, 5', 'hypothyroidism, congenital, due to dyshormonogenesis, 5', 'TDH5', 'familial thyroid dyshormonogenesis caused by mutation in DUOXA2']",0112184,274900,,C0342196,,,,C562771,,,,
mondo:0010138,thyrotoxicosis,"['Graves disease, susceptibility to, 1', 'GRD1', 'GRD', 'hyperthyroidism, autoimmune']",7997,,,C0040156,,C61469,0009190,D013971,242.90,,,
mondo:0010139,isolated thyroid-stimulating hormone deficiency,"['hypothyroidism, congenital, nongoitrous 4', 'congenital nongoitrous hypothryoidism 4', 'thyrotropin deficiency, isolated', 'hypothyroidism, congenital, nongoitrous, 4', 'pituitary cretinism', 'thyrotropin, biologically inactive', 'CHNG4', 'thyroid-stimulating hormone, deficiency of', 'isolated thyrotropin deficiency', 'thyroid-stimulating hormone deficiency', 'hypothyroidism, congenital, nongoitrous, type 4', 'TSH deficiency', 'isolated TSH deficiency', 'congenital nongoitrous hypothyroidism 4']",0070123,275100,90674,C4082174,"['-0.673', '0.05432', '-0.2218', '-0.0819', '0.1417', '0.06494', '-0.2318', '0.318', '-0.56', '-0.5474', '0.04004', '0.06586', '0.01208', '0.574', '-0.1447', '0.2566', '0.3367', '0.008766', '-0.5225', '-0.7607', '-0.1895', '-0.01313', '0.804', '-0.497', '0.2568', '-0.1633', '0.178', '0.1254', '0.4236', '-0.1779', '0.659', '0.196', '0.3008', '0.4375', '-0.3867', '-0.267', '-0.1604', '0.329', '-0.1576', '0.1576', '0.4421', '0.1917', '-0.1307', '0.1757', '0.05573', '-0.06696', '0.847', '0.11', '0.3594', '0.181', '-0.1816', '0.02467', '-0.4802', '-0.2827', '-0.697', '0.6445', '0.2327', '-0.4717', '-0.2446', '0.2382', '0.3782', '0.05365', '-0.1207', '-0.596', '-0.2133', '0.2004', '0.4429', '0.586', '-0.4636', '0.2103', '-0.2625', '0.4993', '0.1678', '-0.3179', '-0.12036', '0.00784', '0.524', '0.003265', '-0.1613', '0.0818', '-0.188', '-0.236', '-0.6636', '-0.586', '0.2319', '0.3442', '0.2286', '-0.03232', '1.256', '-0.1738', '0.1193', '0.707', '0.2092', '-0.2108', '0.5093', '0.2211', '-0.364', '-0.07544', '0.5454', '0.3638']",,,,,,,
mondo:0010140,isolated thyrotropin-releasing hormone deficiency,"['thyrotropin-releasing hormone deficiency', 'isolated TSH-releasing factor deficiency', 'tertiary hypothyroidism', 'hypothalamic hypothyroidism', 'isolated protirelin deficiency', 'isolated prothyroliberin deficiency', 'isolated thyroliberin deficiency', 'isolated TRH deficiency', 'isolated TRF deficiency', 'isolated thyrotropin-releasing factor deficiency', 'TRH deficiency']",,275120,238670,,,C121741,,,253.4,,,
mondo:0010141,tiglic acidemia,"['tiglic acidemia', 'disorder of isoleucine metabolism']",,275190,,C1848793,,,,C536921,270.8,,,
mondo:0010142,hypothyroidism due to TSH receptor mutations,"['thyroid-stimulating hormone, resistance to', 'congenital nongoitrous hypothryoidism 1', 'hypothyroidism, Nonautoimmune', 'thyrotropin resistance', 'hypothyroidism due to unresponsiveness to thyrotropin', 'hypothyroidism, congenital, nongoitrous, 1', 'congenital nongoitrous hypothyroidism 1', 'hypothyroidism, congenital, due to TSH resistance', 'hypothyroidism, congenital, nongoitrous, type 1', 'TSH resistance', 'CHNG1']",0070126,275200,90673,CN206435,"['-0.0599', '0.47', '-0.0812', '-0.010765', '0.4495', '-0.01616', '0.0905', '0.08386', '-0.1628', '-0.5586', '0.02954', '0.03656', '-0.0888', '0.3784', '-0.185', '-0.2776', '-0.1849', '-0.2976', '-0.29', '-0.664', '0.08044', '-0.10114', '0.479', '-0.3374', '0.07764', '0.319', '-0.2379', '-0.1405', '0.4346', '-0.4226', '0.3523', '0.4197', '0.1322', '0.1866', '-0.3455', '-0.56', '0.1138', '0.0277', '-0.4446', '0.0667', '0.3186', '-0.10114', '0.3848', '-0.10516', '0.04163', '-0.07184', '0.6323', '0.2197', '0.534', '0.2698', '0.0793', '-0.293', '-0.0872', '-0.256', '-0.6978', '0.2463', '0.643', '-0.3958', '0.1296', '0.1691', '0.4214', '0.1713', '0.03105', '-0.2405', '0.06067', '0.27', '0.2698', '0.5205', '-0.4792', '-0.0759', '-0.1041', '0.1395', '0.386', '-0.6475', '0.524', '0.01377', '0.1932', '-0.10785', '-0.3347', '0.2169', '-0.325', '0.2627', '-0.4514', '-0.6357', '-0.1321', '0.0585', '0.367', '-0.007145', '0.7495', '-0.04327', '0.329', '0.3252', '-0.173', '-0.2445', '0.853', '0.02022', '0.0993', '-0.4443', '0.1952', '0.2803']",,,,,,,
mondo:0010144,tibial hemimelia,"['congenital longitudinal deficiency of the tibia', 'Thm', 'bilateral absence of the tibia', 'absence of tibia', 'tibial longitudinal meromelia', 'tibia, absence of', 'congenital aplasia and dysplasia of the tibia with intact fibula', 'tibial hemimelia', 'congenital absence of tibia']",,275220,93322,,,,,C535563,,,,
mondo:0010145,"tibia, absence of, with congenital deafness","['tibia, absence of, with congenital deafness']",,275230,,C1848758,,,,C564764,,,,
mondo:0010146,Kerion celsi,"['Trichophyton infection', 'trichophytia profunda barbae', 'TINEA imbricata, susceptibility to', 'Tinea capitis profunda', 'susceptibility to Tinea imbricata', 'trichophytia profunda capitis']",,275240,499,C0276742,,,,,,,,
mondo:0010147,"tongue, pigmented fungiform papillae of","['tongue, pigmented fungiform papillae of']",,275250,,C1848756,,,,,,,,
mondo:0010148,Mounier-Kuhn syndrome,"['Mounier-Kühn syndrome', 'idiopathic tracheobronchomegaly', 'congenital tracheobronchomegaly', 'Mounier Kuhn syndrome', 'tracheobronchomegaly', 'Mounier-Kuhn syndrome']",,275300,3347,C2713583,,C85196,,D014137,748.3,,10044316,
mondo:0010149,transcobalamin II deficiency,"['Tcn2 deficiency', 'TCN2 deficiency', 'transcobalamin II deficiency', 'inherited deficiency of transcobalamin', 'transcobalamin 2 deficiency', 'transcobalamin deficiency', 'TC 2 deficiency']",0050818,275350,859,C0342701,"['-0.1619', '0.1242', '0.02136', '-0.2136', '-0.2708', '-0.3015', '-0.3513', '0.774', '-0.10205', '0.04443', '-0.402', '-0.2097', '0.05048', '-0.0263', '-0.1721', '0.1938', '-0.03687', '0.08405', '-0.3425', '-0.6973', '0.02841', '-0.658', '-0.2246', '-0.2366', '0.268', '-0.02052', '-0.2764', '0.2019', '-0.5254', '-0.657', '-0.4', '-0.07245', '-0.0365', '0.10706', '-0.4624', '0.9775', '-0.3472', '-0.2107', '-0.322', '0.1653', '-0.4653', '-0.03265', '0.746', '0.05234', '-0.06915', '0.02002', '-0.4895', '-0.562', '-0.1373', '0.2339', '-0.06775', '-0.0937', '0.08844', '-0.009575', '-0.2482', '0.1368', '0.5635', '-0.01126', '-0.6494', '0.3044', '0.1037', '0.5054', '-0.1469', '-0.1387', '0.251', '-0.04028', '0.736', '0.2847', '-0.4448', '0.2827', '0.3098', '0.1349', '-0.5225', '0.17', '0.3606', '0.1309', '0.2173', '0.12036', '0.2141', '0.2266', '0.0869', '-0.1317', '0.7114', '0.05527', '0.3074', '0.8457', '0.10846', '0.3813', '0.2184', '0.1522', '0.535', '0.3264', '-0.4268', '-0.4316', '0.999', '0.776', '0.4814', '-0.2832', '-0.09674', '-0.01764']",C142806,,,,D51.2,,
mondo:0010150,head and neck squamous cell carcinoma,"['SCCHN', 'squamous cell carcinoma of the head and neck', 'HNSCC', 'head and neck squamous cell carcinoma', 'squamous cell carcinoma, head and neck', 'squamous cell carcinomas of head and neck', 'squamous cell carcinoma, head and neck, somatic', 'squamous cell carcinoma of head and neck', 'craniocervical region squamous cell carcinoma', 'carcinoma of the head and neck']",5520,275355,67037,C1168401,"['-0.01069', '0.1588', '0.05505', '-0.1985', '-0.1221', '0.01215', '0.2457', '0.0951', '-0.2317', '-0.07465', '-0.04858', '-0.201', '-0.2036', '0.1311', '-0.4985', '-0.01527', '0.00722', '-0.2382', '0.06012', '-0.2139', '-0.06726', '-0.1335', '0.1796', '-0.1898', '0.265', '0.01717', '-0.007236', '0.04446', '-0.0946', '-0.1494', '0.0796', '-0.0504', '0.0877', '-0.1038', '0.1526', '0.0875', '-0.0794', '0.00138', '-0.1571', '-0.2405', '0.0626', '-0.2056', '0.202', '-0.327', '0.01872', '-0.2118', '-0.04373', '0.1659', '-0.02602', '0.03427', '-0.185', '-0.1516', '0.1578', '0.2563', '-0.448', '-0.1913', '0.1238', '0.2471', '-0.2434', '-0.2058', '0.0777', '0.0753', '-0.3936', '0.05807', '0.1755', '0.0677', '0.4824', '0.356', '-0.125', '0.4375', '-0.1137', '0.0727', '0.091', '-0.02502', '-0.0346', '0.1017', '-0.1356', '-0.103', '-0.04898', '-0.382', '-0.438', '0.1255', '-0.081', '-0.07245', '-0.1938', '-0.1346', '-0.0744', '0.1959', '0.2732', '-0.2095', '-0.2104', '0.1727', '0.29', '4.613e-05', '0.4062', '-0.065', '0.1168', '-0.2817', '0.0223', '0.0627']",C34447,0000181,C535575,,,10060121,
mondo:0010151,"tricarboxylic acid cycle, defect of","['tricarboxylic acid cycle, defect of']",,275370,,C1848746,,,,C564762,,,,
mondo:0010152,trichomegaly-retina pigmentary degeneration-dwarfism syndrome,"['eyelashes, long, with mental retardation', 'trichomegaly with intellectual disability, dwarfism and pigmentary degeneration of retina', 'eyelashes, long with intellectual disability', 'trichomegaly with intellectual disability, dwarfism, and pigmentary Degeneration of retina', 'OMCS', 'trichomegaly with mental retardation, dwarfism, and pigmentary Degeneration of retina', 'Oliver McFarlane syndrome', 'eyelashes, long, with intellectual disability', 'long eyelashes-intellectual disability syndrome', 'Oliver-McFarlane syndrome']",0111271,275400,3363,C1848745,"['-0.1589', '0.1267', '-0.375', '-0.4004', '0.522', '-0.0835', '0.10004', '1.286', '-0.861', '-0.8696', '0.2344', '-0.428', '0.4365', '0.2915', '0.129', '-0.556', '0.545', '0.3457', '-0.6724', '-1.195', '-1.592', '0.00509', '0.785', '-0.1755', '0.0912', '-0.515', '-0.492', '-0.0819', '0.482', '-0.3486', '0.129', '-0.521', '-0.3035', '-0.1879', '-0.5596', '-0.3845', '0.06216', '0.0589', '0.4026', '-0.0001363', '0.06055', '0.219', '-0.6143', '-0.3237', '0.3333', '-0.0985', '0.0878', '-0.1185', '0.724', '-0.4011', '0.08966', '0.07227', '-0.527', '0.0677', '-0.2375', '-0.681', '-0.4197', '-0.2028', '0.879', '0.4346', '-0.2776', '0.2214', '-0.2932', '0.4417', '0.011215', '1.415', '0.11017', '0.6924', '-0.371', '0.5605', '-0.6284', '-0.05508', '0.4058', '-1.372', '-0.3845', '0.5786', '-0.2334', '0.5166', '-0.113', '0.419', '-0.2708', '-0.1641', '-0.01884', '0.2666', '0.351', '-0.288', '-0.007587', '-0.04498', '0.599', '0.8096', '0.04688', '-0.02112', '-0.642', '-0.621', '0.623', '-0.2893', '0.275', '-0.1875', '0.7017', '0.03735']",,,C536554,,,,
mondo:0010153,trichoodontoonychial dysplasia,"['trichoodontoonychial dysplasia with bone deficiency', 'trichoodontoonychial dysplasia with bone deficiency in frontoparietal region']",,275450,3355,C3502453,,,,C564760,,,,
mondo:0010154,trigonocephaly-bifid nose-acral anomalies syndrome,"['trigonobrachycephaly, bulbous bifid nose, macrostomia, micrognathia, acral anomalies, and hypotonia', 'trigonocephaly - bifid nose - acral anomalies', 'trigonobrachycephaly, bulbous bifid nose, micrognathia, and abnormalities of the hands and feet']",,275595,3368,C1848743,,,,C564759,,,,
mondo:0010155,Dorfman-Chanarin disease,"['CDS', 'neutral lipid storage disease with ichthyosis', 'DCs', 'ichthyosiform erythroderma with leukocyte vacuolation', 'neutral Lipid storage disease with ichthyosis', 'Dorfman Chanarin syndrome', 'Dorfman-Chanarin syndrome', 'disorder of cornification 12 (neutral lipid storage type)', 'ichthyotic neutral Lipid storage disease', 'Chanarin-Dorfman syndrome', 'triglyceride storage disease with impaired long-chain fatty acid oxidation', 'Chanarin-Dorfman disease', 'neutral lipid storage disease with ichthyotic', 'NLSDI']",,275630,98907,,"['-0.2676', '0.2339', '0.1975', '-0.2073', '0.3745', '-0.1669', '-0.1754', '0.02457', '-0.0489', '0.0916', '-0.08514', '-0.0465', '0.1158', '-0.02954', '-0.3154', '-0.1098', '-0.115', '-0.0854', '-0.153', '-0.4067', '0.2173', '-0.2037', '0.1976', '0.1278', '0.2311', '0.07654', '-0.2357', '-0.00818', '-0.0549', '-0.1282', '0.342', '0.1466', '0.4106', '0.3057', '0.1411', '-0.1793', '-0.4753', '-0.10736', '-0.09955', '-0.288', '-0.2834', '-0.2024', '0.1798', '0.295', '-0.04236', '-0.2021', '0.2031', '0.2013', '-0.1213', '-0.1417', '-0.08923', '0.1405', '0.3147', '-0.2854', '0.00985', '-0.4514', '0.1346', '0.02034', '-0.3374', '-0.06006', '0.1858', '-0.2852', '0.01554', '0.03262', '0.1085', '-0.07416', '0.2407', '0.2484', '-0.1014', '0.1184', '-0.507', '-0.05832', '-0.00944', '0.0614', '0.05856', '-0.05435', '0.00829', '-0.03494', '0.02007', '-0.1772', '-0.01799', '-0.2515', '-0.3638', '0.3188', '0.01749', '0.1057', '0.2837', '0.3125', '0.1873', '0.1636', '0.5337', '0.3347', '0.0848', '0.0175', '0.4126', '0.2625', '0.3267', '-0.2373', '0.4028', '0.226']",,,,,,,
mondo:0010156,Troyer syndrome,"['spastic paraplegia 20 (Troyer syndrome)', 'autosomal recessive spastic paraplegia type 20', 'SPG20', 'spastic paraparesis, childhood-onset, with distal muscle wasting', 'childhood-onset spastic paraparesis-distal muscle wasting syndrome', 'Troyer syndrome', 'hereditary spastic paraplegia 20', 'autosomal recessive spastic paraplegia 20', 'spastic paraplegia 20', 'spastic paraplegia 20, autosomal recessive', 'spastic paraplegia, autosomal recessive, Troyer type', 'spastic paraplegia type 20', 'autosomal recessive spastic paraplegia Troyer type', 'Cross-McKusick syndrome', 'childhood-onset spastic paraparesis with distal muscle wasting']",0050886,275900,101000,C0393559,"['-0.2524', '0.3716', '0.1942', '-0.433', '-0.3364', '-0.795', '-0.528', '0.551', '-0.5894', '-0.4746', '-0.2158', '0.2783', '-0.3047', '0.114', '0.3398', '0.1785', '-0.0719', '-0.4795', '-0.139', '-0.5366', '0.3997', '-0.0983', '0.049', '-0.05563', '0.256', '0.04184', '-0.00596', '0.0443', '-0.0464', '-0.1244', '0.08545', '-0.1346', '0.2957', '-0.05283', '0.05215', '-0.1915', '-0.03087', '-0.3984', '-0.465', '0.002018', '0.0848', '-0.596', '-0.1328', '0.3137', '0.00907', '-0.1592', '-0.02397', '0.3738', '0.1389', '-0.0744', '-0.0676', '0.5273', '-0.738', '-0.3264', '0.2798', '-0.7476', '0.4697', '-0.391', '0.1243', '0.7036', '0.2222', '-0.0628', '0.2399', '0.1272', '-0.6523', '0.1934', '0.1566', '0.3333', '-0.1511', '0.3203', '-0.573', '0.273', '-0.01322', '-0.1683', '0.6514', '0.29', '-0.1425', '0.0911', '-0.2517', '-0.051', '0.3513', '-0.0759', '0.4548', '0.469', '-0.01359', '0.2703', '0.0367', '0.457', '0.4573', '-0.1053', '0.0642', '0.4731', '0.0007186', '-0.2219', '0.5366', '0.276', '0.352', '-0.2537', '0.388', '0.0767']",,,C536858,335.29,,,
mondo:0010157,Tryptophanuria with dwarfism,['Tryptophanuria with dwarfism'],,276100,,C0268473,,,,C562658,259.4,,,
mondo:0010158,T-substance anomaly,['T-substance anomaly'],,276200,,,,,,,,,,
mondo:0010159,mismatch repair cancer syndrome 1,"['MMRCS', 'BTP1 syndrome', 'brain tumor-polyposis syndrome', 'MMR deficiency', 'MMRCS1', 'CNS tumors with familial polyposis of the colon', 'mismatch repair cancer syndrome', 'CMMR-D syndrome', 'mismatch repair deficiency', 'glioma-polyposis syndrome', 'CMMR-D', 'Turcot syndrome', 'CNS tumours with familial polyposis of the colon', 'malignant tumors of the central nervous system associated with familial polyposis of the colon', 'brain tumor-polyposis syndrome 1', 'constitutional MIS-match repair deficiency syndrome', 'malignant tumours of the central nervous system associated with familial polyposis of the colon', 'constitutional mismatch repair deficiency syndrome', 'childhood cancer syndrome']",,276300,252202,C4321324,"['0.3145', '-0.02518', '0.11487', '-0.5967', '0.596', '-0.2012', '0.2456', '0.2285', '-0.3997', '-0.552', '-0.1683', '0.5586', '0.1346', '-0.09106', '-0.3462', '-0.0626', '-0.141', '-0.3555', '-0.464', '-0.386', '-0.2009', '-0.504', '0.2864', '-0.606', '0.14', '-0.2817', '-0.05124', '0.02061', '0.2715', '-0.5205', '0.354', '-0.4248', '0.508', '0.3398', '0.3357', '0.0508', '-0.412', '0.2401', '-0.2413', '0.0443', '0.10504', '-0.4922', '0.3171', '-0.3643', '0.1287', '-0.3757', '0.1929', '0.2042', '0.3677', '-0.3228', '0.1549', '0.363', '-0.541', '0.359', '0.02051', '0.1522', '-0.151', '-0.03415', '-0.3796', '0.5522', '0.2832', '0.2119', '0.04858', '0.1561', '-0.03674', '0.51', '0.6226', '0.4111', '0.2593', '1.035', '-0.3796', '-0.0811', '-0.11426', '0.424', '0.4297', '-0.2412', '-0.1296', '0.2361', '-0.1466', '-0.4602', '0.11005', '0.4243', '0.2214', '0.1345', '-0.5967', '-0.2905', '0.8965', '0.2456', '0.1624', '-0.4482', '0.3765', '0.5806', '0.2654', '-0.3887', '0.2157', '0.1957', '0.3499', '-0.236', '0.2177', '0.03522']",C130202,,C536928,,,,
mondo:0010160,tyrosinemia type II,"['tyrosinemia due to TAT deficiency', 'keratosis palmoplantaris with corneal dystrophy', 'tyrosinemia due to tyrosine aminotransferase deficiency', 'Tyrosinosis oculocutaneous type', 'Oregon type tyrosinemia', 'tyrosinemia, type II', 'Richner Hanhart syndrome', 'tyrosinemia type II', 'Richner-Hanhart syndrome', 'TYRSN2', 'tyrosine aminotransferase deficiency', 'Tat deficiency', 'keratosis palmoplantaris-corneal dystrophy syndrome', 'tyrosine transaminase deficiency', 'tyrosinemia type 2', 'tyrosinemia, type 2', 'oculocutaneous tyrosinemia', 'Tyrosinosis, oculocutaneous type']",0050725,276600,28378,,"['-0.1925', '0.274', '-0.769', '-0.2568', '0.1674', '-0.4968', '-0.3882', '-0.1034', '-0.545', '0.2634', '-0.533', '0.1449', '-0.2686', '-0.0616', '-0.4792', '-0.007744', '0.9277', '-0.03528', '0.001959', '-1.056', '-0.06366', '-0.1957', '0.003504', '-0.03653', '-0.4492', '0.2354', '-0.04913', '0.2058', '0.00256', '0.1852', '0.4253', '-0.4446', '-0.2335', '0.2208', '-0.2908', '0.2874', '-0.4824', '-0.02452', '-0.05878', '0.6577', '0.684', '-0.4392', '0.3162', '0.3452', '-0.0358', '0.2139', '0.5835', '-0.664', '-0.1249', '-0.2258', '-0.1897', '0.5605', '0.2012', '-0.615', '-0.449', '0.6826', '0.8994', '-0.28', '-0.4988', '-0.2688', '0.3137', '-0.03424', '-0.3416', '-0.1499', '0.182', '-0.06177', '0.3354', '0.733', '0.03442', '0.3213', '-0.347', '0.2328', '-0.1638', '-0.0317', '0.5674', '0.78', '0.2979', '-0.479', '0.2625', '-0.2651', '0.03702', '-0.1588', '0.0065', '0.4739', '0.411', '0.2903', '-0.5566', '0.8145', '0.275', '0.5527', '0.428', '0.3042', '0.3408', '-0.5425', '0.7007', '0.0775', '0.06726', '-0.5654', '0.342', '0.1881']",C129032,,,,,10069463,
mondo:0010161,tyrosinemia type I,"['TYRSN1', 'fumarylacetoacetase deficiency', 'fumarylacetoacetate hydrolase deficiency', 'tyrosinemia type 1', 'Fah deficiency', 'hepatorenal tyrosinemia', 'tyrosinemia type I', 'tyrosinemia, type 1', 'type I tyrosinemia', 'FAH deficiency', 'tyrosinemia, type I']",0050726,276700,882,C0268490,"['0.1144', '-0.0962', '-0.3613', '-0.0747', '-0.5312', '-0.4045', '0.00766', '0.4084', '-0.003174', '0.4194', '-0.06213', '0.1583', '0.2808', '0.5225', '-0.3137', '-0.2261', '0.3389', '-0.4312', '0.0474', '-0.8467', '-0.03516', '-0.2432', '0.905', '0.0613', '-0.3665', '0.2527', '0.4138', '0.392', '-0.2668', '0.1207', '-0.1552', '0.006382', '0.3865', '-0.154', '-0.489', '-0.05838', '-0.3994', '-0.1302', '0.01524', '0.235', '-0.487', '-0.2156', '0.7925', '0.1008', '-0.2056', '0.3508', '-0.7407', '-0.7437', '0.11237', '0.03302', '0.2876', '0.2351', '0.039', '-0.323', '-0.2172', '-0.922', '0.67', '0.081', '-0.4314', '0.2668', '0.4707', '0.3796', '0.525', '-0.2751', '0.225', '0.2465', '0.6763', '0.2578', '0.006073', '0.1843', '-0.2969', '-0.0638', '0.05954', '-0.5356', '0.225', '0.3896', '0.2627', '-0.4744', '-0.2216', '-0.2262', '-0.1862', '0.02675', '-0.3496', '-0.3203', '0.04675', '0.6396', '0.5337', '0.0554', '0.7627', '-0.0711', '0.3545', '0.02974', '0.0879', '-0.0857', '0.279', '0.5796', '-0.05835', '-0.604', '-0.1069', '0.0954']",C98641,,,,,10069462,
mondo:0010162,tyrosinemia type III,"['tyrosinemia due to 4-hydroxyphenylpyruvate dioxygenase deficiency', 'tyrosinemia, type 3', '4-Hydroxyphenylpyruvic acid oxidase deficiency', '4-alpha hydroxyphenylpyruvic acid oxidase deficiency', 'tyrosinemia, type III', 'TYRSN3', 'tyrosinemia due to 4-hydroxyphenylpyruvic acid oxidase deficiency', 'tyrosinemia due to HPD deficiency', 'tyrosinemia type III', 'tyrosinemia type 3', '4-Hydroxyphenylpyruvate dioxygenase deficiency', '4-alpha hydroxyphenylpyruvate dioxygenase deficiency']",0050727,276710,69723,C0268623,"['0.2053', '0.2172', '-0.366', '0.375', '0.327', '-0.291', '-0.2233', '0.3816', '-0.509', '0.2156', '-0.3843', '-0.0866', '0.1615', '-0.3203', '0.1087', '-0.06113', '0.238', '0.01968', '-0.2712', '-0.349', '0.01125', '-0.04636', '0.275', '-0.1865', '-0.04962', '0.0796', '-0.1943', '-0.06113', '0.1694', '-0.04916', '0.2869', '0.2576', '0.2578', '0.3455', '-0.5938', '-0.316', '-0.3362', '-0.3274', '-0.189', '-0.05374', '0.3992', '-0.7974', '0.41', '-0.327', '-0.0842', '-0.084', '0.0602', '-0.172', '-0.0892', '-0.501', '-0.161', '-0.25', '-0.1113', '-0.3938', '0.02332', '-0.05508', '0.3213', '-0.2712', '-0.3118', '-0.2076', '0.4412', '0.088', '0.3972', '-0.1289', '0.2042', '-0.002453', '0.3062', '0.3186', '-0.2207', '0.1525', '0.00175', '0.3162', '0.001614', '-0.002748', '0.303', '0.1769', '-0.0673', '-0.281', '-0.04053', '0.0628', '0.1797', '0.0948', '-0.15', '0.4185', '0.2473', '0.633', '-0.00402', '0.11017', '0.3777', '0.1526', '0.5005', '0.4553', '-0.2695', '-0.2217', '0.8926', '0.5283', '0.1617', '-0.3188', '0.1625', '-0.011765']",,,,270.2,,10069461,
mondo:0010163,Tyrosinosis,['Tyrosinosis'],,276800,,C0268484,,,,C562659,270.2,,,
mondo:0010164,"phocomelia, Schinzel type","['Al-Awadi/Raas-Rothschild/Schinzel phocomelia syndrome', 'aplasia/hypoplasia of limbs and pelvis', 'Schinzel phocomelia syndrome', 'Al-Awadi/Raas-Rothschild syndrome', 'profound limb deficiency, thoracic dystrophy, unusual facies, and normal intelligence', 'Al Awadi Teebi Farag syndrome', 'Teebi Naguib Al Awadi syndrome', 'congenital absence of ulna and fibula', 'limb/pelvis-hypoplasia/aplasia syndrome', 'AARRS', 'Al Awadi-Raas-Rothschild syndrome', 'ulna and fibula absence of with severe limb deficiency', 'absence of ulna and fibula with severe limb deficiency', 'severe limb deficit', 'Al-Awadi-Raas-Rothschild syndrome', 'ulna and fibula, absence of, with severe limb deficiency']",0112181,276820,2879,,"['-0.36', '-0.5957', '0.4932', '-0.8467', '0.2817', '-0.1418', '-0.01181', '0.4783', '-0.4468', '-0.6025', '-0.5317', '-0.561', '-0.4167', '0.3232', '-0.4788', '-0.1215', '0.384', '-0.3472', '-0.6', '-0.3105', '0.3604', '0.1517', '0.55', '-0.2242', '0.10284', '-0.1178', '-0.2291', '-0.4966', '0.4807', '-0.3142', '0.7017', '-0.2045', '-0.0493', '0.3267', '0.2256', '-0.0787', '-0.1678', '-0.1838', '-0.5054', '-0.3389', '0.1713', '-0.3198', '-0.02017', '-0.2998', '-0.1002', '-0.5503', '-0.007034', '0.2494', '-0.3193', '0.1449', '0.1498', '-0.199', '0.02766', '0.3325', '-0.6665', '-0.3157', '-0.424', '-0.4385', '-0.1875', '0.4153', '0.0006847', '-0.3726', '-0.0666', '0.2646', '-0.347', '0.1909', '0.2152', '0.5527', '-0.2407', '0.295', '-0.3413', '0.1488', '0.48', '0.2556', '0.1334', '0.4124', '-0.1566', '-0.0618', '-0.3154', '-0.4734', '-0.3584', '0.537', '0.431', '0.09326', '-0.463', '0.06976', '0.2211', '0.4062', '-0.0402', '-0.4614', '-0.3438', '0.4788', '0.327', '0.4683', '0.4495', '-0.0766', '0.1804', '-0.808', '0.2223', '0.1355']",,,C535612,,,,
mondo:0010165,ulna hypoplasia-intellectual disability syndrome,"['mesomelia of the upper limbs, absent nails, clubfeet, and mental retardation', 'ulnar hypoplasia with mental retardation', 'ulna hypoplasia with mental retardation', 'bilateral ulnar hypoplasia and intellectual disability', 'mesomelia of the upper limbs, anonychia congenita, clubfeet, and mental retardation', 'bilateral ulnar hypoplasia and mental retardation', 'mesomelia of the upper limbs, anonychia congenita, clubfeet, and intellectual disability', 'mesomelia of the upper limbs, absent nails, clubfeet, and intellectual disability', 'ulna hypoplasia with intellectual disability', 'ulnar hypoplasia with intellectual disability']",,276821,2249,C2931370,,,,C564757,,,,
mondo:0010166,ulnar agenesis and endocardial fibroelastosis,['ulnar agenesis and endocardial fibroelastosis'],,276822,,C1848649,,,,C564756,,,,
mondo:0010167,urocanic aciduria,"['urocanic aciduria', 'urocanic aciduria (disease)', 'encephalopathy due to urocanase deficiency', 'UROCD', 'urocanase deficiency']",0112180,276880,210128,C0268514,"['-0.33', '0.1648', '-0.1259', '-0.1216', '0.01979', '-0.263', '-0.2786', '0.2585', '-0.0983', '0.04785', '-0.2303', '-0.02187', '0.1498', '-0.2047', '0.03268', '-0.149', '0.1418', '0.0624', '-0.2922', '-0.557', '-0.0829', '-0.2778', '0.2544', '-0.3225', '-0.0041', '-0.03104', '0.012024', '-0.1079', '-0.1605', '-0.1613', '0.094', '0.10046', '0.374', '0.2578', '-0.4634', '-0.1683', '-0.02766', '-0.1489', '-0.2163', '-0.1172', '-0.03232', '-0.6104', '0.216', '-0.4019', '-0.237', '-0.3506', '0.348', '0.1071', '-0.1105', '0.02791', '-0.2449', '0.11194', '-0.1085', '-0.3164', '-0.1006', '-0.03123', '0.3794', '-0.2134', '-0.3845', '0.238', '0.3025', '0.01031', '0.285', '-0.0761', '0.01863', '-0.10974', '0.2715', '0.10986', '-0.3462', '0.08325', '-0.24', '0.1461', '-0.2693', '-0.1606', '-0.02875', '0.3147', '0.314', '-0.0647', '0.01851', '0.1118', '0.1335', '-0.11066', '0.01747', '0.261', '0.4543', '0.225', '-0.03415', '0.1143', '0.3022', '0.133', '0.352', '0.344', '-0.3337', '-0.1014', '0.5933', '0.6064', '0.317', '-0.2537', '0.067', '0.1882']",,,C536479,,,,0012237
mondo:0010168,Usher syndrome type 1,"['USH1', 'retinitis pigmentosa and congenital deafness', 'Usher syndrome, type 1B', 'Usher syndrome, type I, French variety, formerly', 'Usher syndrome, type Ia', 'Usher syndrome, type 1', 'USH1A', 'Usher syndrome, type Ia, formerly', 'Usher syndrome, type I, French variety', 'USHER syndrome, type I', 'US1', 'Usher syndrome, type 1A']",0110826,,231169,,"['-0.3416', '0.02095', '0.3186', '0.1233', '0.03485', '-0.3643', '-0.1545', '0.377', '-0.419', '-0.2065', '-0.1715', '-0.05188', '-0.145', '-0.02597', '0.2024', '-0.4119', '0.1554', '0.0317', '0.1903', '-0.572', '-0.1132', '-0.2654', '-0.0577', '0.2137', '0.2186', '-0.0688', '-0.635', '-0.3435', '-0.3076', '0.1399', '0.3599', '0.36', '0.00946', '0.1382', '-0.0669', '-0.2277', '-0.1569', '-0.1249', '-0.1873', '-0.05487', '-0.01463', '-0.1873', '-0.2247', '0.1483', '-0.1871', '0.2766', '-0.1055', '-0.0699', '0.1316', '0.595', '0.2262', '0.1935', '0.11444', '-0.532', '0.3997', '-0.0941', '0.3945', '-0.1527', '-0.349', '0.0524', '0.135', '0.1654', '0.11127', '0.3884', '-0.0648', '0.1204', '0.02316', '0.4', '-0.2607', '0.3005', '-0.3933', '0.2976', '0.1923', '-0.6953', '0.6504', '-0.675', '-0.02957', '0.1682', '-0.116', '-0.1473', '0.3218', '-0.3257', '-0.000998', '0.8003', '-0.2612', '-0.03305', '-0.012634', '0.0702', '0.3635', '0.222', '0.2075', '0.4966', '0.3801', '0.4033', '0.1385', '0.2247', '0.2269', '-0.494', '-0.000717', '0.4805']",C126327,,,,H35.5,,
mondo:0044789,digital papillary eccrine carcinoma,"['digital papillary eccrine carcinoma', 'digit papillary eccrine carcinoma', 'digital papillary carcinoma', 'papillary eccrine carcinoma of digit', 'papillary digital eccrine carcinoma']",,,,,,C27534,,,,,,
mondo:0044791,combined hepatocellular carcinoma and cholangiocarcinoma,"['Cholangiohepatoma', 'carcinoma of the liver and intrahepatic biliary tract', 'combined hepatocellular cancer and intrahepatic bile duct cancer (cholangiocarcinoma)', 'Mixed hepatocellular cholangiocarcinoma', 'liver and intrahepatic biliary tract carcinoma', 'carcinoma of liver and intrahepatic biliary tract', 'Hepatocholangiocarcinoma', 'combined hepatocellular cancer and cholangiocarcinoma (bile duct cancer)', 'combined hepatocellular carcinoma and cholangiocarcinoma']",,,529852,,,C3828,,,,,,
mondo:0044792,large congenital melanocytic nevus,"['congenital giant pigmented nevus', 'spitz nevus or nevus spilus, somatic', 'giant congenital nevus', 'congenital melanocytic nevus of skin', 'large congenital melanocytic nevus', 'GMN', 'congenital melanocytic nevus', 'congenital hairy nevus', 'nevus spilus', 'giant hairy nevus', 'melanocytic nevus syndrome, congenital, somatic', 'congenital pigmented nevus of skin', 'pigmented moles', 'giant pigmented nevus of skin', 'melanocytic nevus syndrome, congenital', 'congenital melanocytic nevi', 'CMNS', 'bathing trunk nevus', 'congenital melanocytic nevus of the skin', 'giant congenital melanocytic nevus', 'giant congenital pigmented Nevus', 'congenital pigmented melanocytic Nevus', 'giant pigmented nevus of the skin', 'congenital skin nevus', 'giant pigmented nevus', 'congenital pigmented skin nevus', 'congenital pigmented nevus', 'congenital nevus of the skin', 'GPHN', 'LCMN', 'congenital nevus', 'giant pigmented hairy nevus', 'congenital pigmented nevus of the skin', 'congenital nevus of skin', 'spitz nevus']",0111359,137550,626,C1842036,"['-0.0597', '0.0646', '0.01738', '-0.03983', '0.07605', '-0.08716', '-0.005764', '0.09296', '-0.10443', '-0.02055', '0.00868', '0.01479', '0.0343', '0.01785', '-0.06226', '-0.02632', '0.004845', '-0.065', '-0.00626', '-0.1699', '-0.02058', '0.0001194', '0.08636', '-0.05588', '0.03052', '-0.02391', '-0.02708', '-0.025', '0.05444', '-0.08856', '0.1217', '-0.04156', '0.1101', '0.04028', '0.01836', '-0.014', '-0.0193', '-0.05096', '-0.02058', '-0.10406', '0.061', '-0.10364', '0.0339', '-0.05475', '0.003143', '-0.05533', '-0.01826', '0.0832', '0.002563', '0.001339', '-0.003174', '-0.007603', '0.011406', '-0.00973', '-0.0741', '-0.03867', '0.0846', '-0.01491', '-0.1292', '0.006443', '0.06683', '0.0339', '-0.03326', '0.0348', '0.001072', '-0.001074', '0.11847', '0.07947', '-0.0673', '0.1141', '-0.0298', '0.04117', '0.04562', '-0.03967', '0.03745', '0.0688', '0.00708', '-0.0384', '-0.0569', '-0.081', '-0.02762', '-0.00046', '0.001818', '0.0803', '-0.02435', '-0.01266', '0.03363', '0.0601', '0.0661', '-0.0342', '0.03055', '0.10406', '0.03683', '0.005196', '0.1901', '-0.01211', '0.07806', '-0.1371', '0.01573', '0.03268']",C4234,,,,,10072036,
mondo:0044793,spitz nevus,"['benign juvenile melanoma', 'spitz nevi', 'juvenile nevus', 'spindle and/ or epithelioid cell Nevus', 'spitz nevus', 'spitz naevus']",,,,,,C27007,,,,,,
mondo:0044794,benign melanocytic skin nevus,"['benign melanocytic skin nevus', 'benign melanocytic nevus of the skin', 'benign mole', 'benign nevus of the skin', 'benign nevus of skin', 'benign melanocytic nevus', 'benign skin nevus', 'benign melanocytic nevus of skin']",,,,C1456781,,C7571,,,,,,
mondo:0044795,epithelioid cell nevus,['epithelioid cell nevus'],,,,C0259820,,C66757,,,,,,
mondo:0044796,spindle cell nevus,['spindle cell nevus'],,,,,,C66758,,,,,,
mondo:0044797,desmoplastic nevus,['Desmoplastic Nevus'],,,,C0346098,,C4497,,,,,,
mondo:0044800,desmoplastic spitz nevus,['Desmoplastic spitz Nevus'],,,,C1275419,,C82864,,,,,,
mondo:0044807,inherited dystonia,"['rare genetic dystonic disorder', 'rare genetic dystonia', 'familial dystonia', 'hereditary dystonic disorder']",,,391799,CN227322,,C35527,,,,,,
mondo:0044811,idiopathic torsion dystonia,['Idiopathic torsion dystonia'],,,,,,C34564,,,333.6,,,
mondo:0044816,familial idiopathic torsion dystonia,"['hereditary idiopathic torsion dystonia', 'familial Idiopathic dystonia']",,,,,,C35437,,,,,,
mondo:0044817,acquired idiopathic torsion dystonia,"['acquired idiopathic torsion dystonia', 'non-Familial Idiopathic dystonia']",,,,,,C35438,,,,,,
mondo:0044843,torsion dystonia,,,,,,,,,,,,,
mondo:0044870,acquired torsion dystonia,['acquired torsion dystonia'],,,,C1719382,,,,,,,,
mondo:0044871,"dystonia, focal, task-specific","['FTSD', 'focal hand dystonia', 'task-specific dystonia', 'task-specific focal dystonia', 'musician^s cramp', 'musician^s dystonia', 'occupational dystonia', 'dystonia, focal, task-specific', 'focal task-specific dystonia', 'occupational cramp']",,611284,,,,,,C566973,,,,
mondo:0044872,dysautonomia,['dysautonomia'],,,,,,C53439,,,,,,
mondo:0044873,childhood myelodysplastic syndrome,"['childhood MDS', 'childhood myelodysplastic syndrome', 'myelodysplastic syndrome']",,,,,,C68744,,,,,,
mondo:0044874,refractory cytopenia of childhood,"['RCC', 'refractory cytopenia of childhood']",,,,,,C82596,,,,,,
mondo:0044875,coronary microvascular disorder,"['microvascular endothelium heart disease', 'CMD', 'coronary microvascular disease']",,,,,,C84478,,,,,,
mondo:0044876,drug hypersensitivity syndrome,"['Drug hypersensitivity syndrome', 'Drug reaction with eosinophilia and Systemic symptoms', 'dress', 'DHS']",,,,,,C112208,,D063926,,,,
mondo:0044877,paraneoplastic cerebellar degeneration,['paraneoplastic cerebellar degeneration'],,,623626,,,C4685,,D020362,,,,
mondo:0044878,adult germ cell tumor,"['germ cell tumor', 'germ cell tumour of adults', 'germ cell tumour', 'Adult germ cell tumour', 'germ cell tumor of adults', 'Adult germ cell tumor']",,,,,,C114777,,,,,,
mondo:0044879,pancreatic mucinous-cystic neoplasm,"['mucinous cystic neoplasm', 'Pancreatic mucinous cystic neoplasm', 'Pancreatic mucinous-cystic neoplasm']",,,,,,C41247,,,,,,
mondo:0044880,cystic tumor of the pancreas,,,,,,,,,,,,,
mondo:0044881,hematopoietic and lymphoid cell neoplasm,"['haematopoietic cell tumour', 'haematopoietic neoplasm', 'haematopoietic and lymphoid neoplasms', 'hematopoietic cell tumor', 'hematopoietic neoplasms including lymphomas', 'haematopoietic tumour', 'malignant hematologic neoplasm', 'hematological neoplasm', 'haematopoietic neoplasms including lymphomas', 'hematopoietic and lymphoid neoplasms', 'haematological tumour', 'haematological neoplasm', 'hematologic neoplasm', 'hematopoietic neoplasm', 'malignant haematopoietic neoplasm', 'HEMOLYMPHORETICULAR tumor, malignant', 'hematological tumor', 'haematopoietic malignancy, NOS', 'haematopoietic cancer', 'hematologic malignancy', 'hematopoietic malignancy, NOS', 'hematopoietic tumor', 'hematopoietic, Including myeloma', 'malignant hematopoietic neoplasm', 'hematopoietic and lymphoid cell neoplasm', 'hematologic cancer', 'hematopoietic cancer']",,,,,,C27134,,,,,,
mondo:0044884,tonsillar lymphoma,"['lymphoma of the tonsil', 'tonsillar lymphoma', 'tonsil lymphoma', 'lymphoma of tonsil', 'Primary tonsillar lymphoma']",,,,C1336765,,C5918,,,,,,
mondo:0044885,tonsillar lipoma,"['lipoma of tonsil', 'lipoma of the tonsil', 'tonsillar lipoma', 'tonsil lipoma']",,,,C1336764,,C5989,,,,,,
mondo:0044887,central nervous system non-hodgkin lymphoma,"['central nervous system non-Hodgkin lymphoma', 'Central nervous system non-Hodgkin lymphoma', 'Primary Central nervous system non-Hodgkin lymphoma', 'non-Hodgkin lymphoma of central nervous system']",,,,C2213246,,C114779,,,,,,
mondo:0044889,high grade B-cell lymphoma,"['high grade B-cell lymphoma', 'HGBL', 'high-grade B-cell lymphoma']",,,,C0456863,,C138211,,,,,,
mondo:0044903,myelofibrosis,['myelofibrosis'],,,,,,C3248,,,,,,
mondo:0044906,bladder urothelial papilloma,"['bladder urothelial papilloma', 'urinary bladder urothelial papilloma', 'bladder transitional cell papilloma', 'urinary bladder transitional cell papilloma']",,,,,,C39858,,,,,,
mondo:0044907,metastatic squamous cell carcinoma,['Metastatic squamous cell carcinoma'],,,,C0334246,,C4104,,,,,,
mondo:0044912,metastatic malignant neoplasm in the spinal cord,"['Metastatic malignant neoplasm to the spinal cord', 'Metastatic neoplasm to the spinal cord', 'Metastatic malignant neoplasm in the spinal cord', 'Metastatic tumor to the spinal cord', 'Secondary malignant neoplasm to the spinal cord', 'Secondary malignant tumor to the spinal cord', 'Secondary malignant tumour to the spinal cord', 'metastasis to spinal cord', 'Metastatic tumour to the spinal cord']",,,,C0347016,,C4585,,,,,,
mondo:0044913,metastatic malignant neoplasm in the eye,"['metastasis to eye', 'Metastatic malignant neoplasm in the eye', 'Metastases to eye', 'Metastases to the eye', 'Metastatic tumor to the eye', 'Metastatic tumour to the eye', 'eye metastasis', 'Metastatic neoplasm to the eye', 'Metastatic malignant neoplasm to the eye', 'metastasis to the eye']",,,,C0347019,,C4586,,,,,,
mondo:0044915,salivary duct carcinoma,"['carcinoma of the salivary duct', 'salivary duct carcinoma', 'carcinoma of duct of salivary gland', 'carcinoma of salivary duct', 'high grade salivary duct carcinoma']",,,,C1301194,,C5904,,,,,,
mondo:0044916,extrarenal rhabdoid tumor,"['extrarenal rhabdoid tumor', 'malignant extrarenal rhabdoid neoplasm', 'rhabdoid tumour of soft tissue', 'rhabdoid tumor of soft tissue']",,,,C1304517,,C6586,,,,,,
mondo:0044917,T-lymphoblastic lymphoma,"['T Lymphoblastic lymphoma', 'Precur. T-lymphoblastic lymphoma', 'precursor T-cell Lymphoblastic lymphoma', 'precursor T-Lymphoblastic lymphoma', 'precursor T Lymphoblastic lymphoma', 'T-lymphoblastic lymphoma', 'precursor T-lymphoblastic lymphoma', 'T-Lymphoblastic lymphoma']",,,,,,C6919,1001830,,,,,
mondo:0044919,malignant renal pelvis neoplasm,"['malignant renal pelvis tumour', 'malignant tumour of the renal pelvis', 'cancer of renal pelvis', 'malignant tumor of renal pelvis', 'malignant tumour of renal pelvis', 'malignant neoplasm of renal pelvis', 'malignant tumor of the renal pelvis', 'malignant renal pelvis neoplasm', 'malignant neoplasm of the renal pelvis', 'malignant renal pelvis tumor']",,,,,,C7525,,,,,,
mondo:0044921,atypical lymphoproliferative disorder,"['atypical lymphoproliferative disorder', 'atypical lymphoid hyperplasia']",,,,C0272217,,C7764,,,,,,
mondo:0044923,acute myeloid leukemia with mutated NPM1,"['acute myeloid leukemia, NPM1 gene mutation', 'NPMc+ AML', 'AML, Nucleophosmin Gene Mutation', 'acute myeloid leukemia with cytoplasmic nucleophosmin', 'AML, Mutation of the Nucleophosmin Gene', 'AML, NPM1 Mutation', 'acute myeloid leukaemia with cytoplasmic nucleophosmin', 'AML with mutated NPM1', 'acute myeloid leukemia with mutated NPM1', 'AML, NPM1 gene mutation']",0081089,,,C2826177,,C82431,,,,,,
mondo:0044925,oral cavity carcinoma,"['oral cavity carcinoma', 'carcinoma of mouth', 'carcinoma of oral cavity', 'oral cavity cancer', 'carcinoma of the oral cavity', 'mouth carcinoma']",,,,C0151546,,C8990,,,,,,
mondo:0044926,oropharyngeal carcinoma,"['oropharyngeal carcinoma', 'cancer of the oropharynx', 'oropharyngeal throat cancer', 'oropharynx carcinoma', 'cancer of oropharynx', 'carcinoma of oropharynx', 'carcinoma of the oropharynx', 'oropharyngeal cancer']",,,,,,C9105,,,,,,
mondo:0044937,rectal carcinoma,"['cancer of the rectum', 'cancer of rectum', 'rectal carcinoma', 'carcinoma of the rectum', 'rectal cancer', 'carcinoma of rectum']",,,,,,C9382,,,,,,
mondo:0044956,paranasal sinus mucoepidermoid carcinoma,"['accessory sinus mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of accessory sinus', 'mucoepidermoid carcinoma of the paranasal sinus', 'mucoepidermoid carcinoma of the accessory sinus', 'mucoepidermoid carcinoma of paranasal sinus', 'paranasal sinus mucoepidermoid carcinoma']",,,,,,C6018,,,,,,
mondo:0044964,oral cavity mucoepidermoid carcinoma,"['mucoepidermoid carcinoma of the oral cavity', 'mucoepidermoid carcinoma of oral cavity', 'oral cavity mucoepidermoid cancer', 'oral cavity mucoepidermoid carcinoma']",,,,C0280309,,C8177,,,,,,
mondo:0044970,mitochondrial disease,,,,,,,,,,,,,
mondo:0044972,eosinophil disorder,"['disease of eosinophil', 'eosinophil disease or disorder', 'disorder of eosinophil']",,,,C1691020,,,,,,,,
mondo:0044981,pseudoallergy,,,,,C3662273,,,,,V15.09,,,
mondo:0044982,drug pseudoallergy,"['drug pseudoallergy', 'drug allergy']",,,,C3662272,,,,,,,,
mondo:0044983,benign lipomatous neoplasm,"['benign neoplasm of the adipose tissue', 'benign neoplasm of adipose tissue', 'benign tumor of adipose tissue', 'benign lipomatous neoplasm', 'benign adipose tissue tumor', 'benign adipose tissue tumour', 'benign adipose tissue neoplasm', 'benign lipomatous tumor', 'benign tumour of adipose tissue', 'benign tumor of the adipose tissue', 'benign tumour of the adipose tissue', 'benign lipomatous tumour', 'adipose tissue benign connective and soft tissue neoplasm', 'benign connective and soft tissue neoplasm of adipose tissue']",,,,,,C4502,,,,,,
mondo:0044984,nasolacrimal duct disorder,"['nasolacrimal duct disease or disorder', 'disease of nasolacrimal duct', 'disorder of nasolacrimal duct', 'nasolacrimal duct disease']",,,,C0521744,,,,,,,,
mondo:0044986,lymphoid system disorder,"['lymphoid system disease or disorder', 'lymphoid system disease', 'disorder of lymphoid system', 'disease of lymphoid system']",,,,,,,,,,,,
mondo:0044991,upper digestive tract disorder,"['disease of upper digestive tract', 'disorder of upper gastrointestinal tract', 'disorder of upper digestive tract', 'upper gastrointestinal tract disease', 'upper digestive tract disease or disorder']",,,,,,,,,,,,
mondo:0044992,mouth mucosa disorder,"['disease of mouth mucosa', 'oral mucous membrane disease', 'disorder of mouth mucosa', 'disorder of oral mucous membrane', 'mouth mucosa disease or disorder']",,,,C1290071,,,,,,,,
mondo:0044993,sympathetic nervous system disorder,"['disease of sympathetic nervous system', 'disorder of sympathetic nervous system', 'sympathetic nervous system disease or disorder', 'sympathetic nervous system disease']",,,,,,,,,,,,
mondo:0044995,parasympathetic nervous system disorder,"['parasympathetic nervous system disease', 'disease of parasympathetic nervous system', 'parasympathetic nervous system disease or disorder', 'disorder of parasympathetic nervous system']",,,,,,,,,,,,
mondo:0044996,cerebral cortex disorder,"['disease of cerebral cortex', 'cerebral cortex disease or disorder', 'cerebral cortex disease', 'disorder of cerebral cortex']",,,,C1263847,,,,,,,,
mondo:0044997,midbrain disorder,"['disorder of midbrain', 'disease of midbrain', 'midbrain disease', 'midbrain disease or disorder']",,,,C0521655,,,,,,,,
mondo:0045001,cardiac ventricle disorder,"['disease of cardiac ventricle', 'cardiac ventricle disease', 'disorder of cardiac ventricle', 'cardiac ventricle disease or disorder']",,,,C1562298,,,,,,,,
mondo:0045002,vertebral disorder,"['disorder of vertebra', 'vertebra disease or disorder', 'disease of vertebra', 'vertebra disease']",,,,C2316319,,,,,,,,
mondo:0045003,scrotal disorder,"['disorder of scrotum', 'scrotum disease or disorder', 'scrotum disease', 'disease of scrotum']",,,,C0268919,,,,,,,,
mondo:0045004,skeletal ligament disorder,"['disease of skeletal ligament', 'disorder of skeletal ligament', 'skeletal ligament disease or disorder']",,,,,,,,,,,,
mondo:0045008,cholesterol metabolism disease,"['disorder of cholesterol metabolic process', 'cholesterol metabolism disease', 'cholesterol metabolic process disease', 'disorder of cholesterol metabolism']",,,,C0342877,,,,,,,,
mondo:0045010,glycoprotein metabolism disease,"['disorder of glycoprotein metabolic process', 'glycoprotein metabolic process disease', 'glycoprotein metabolism disease', 'disorder of glycoprotein metabolism']",,,,C0342844,,,,,,,,
mondo:0045011,keratinization disease,"['disorder of keratinization', 'keratinization disease']",,,,C0475811,,,,,,,,
mondo:0045012,steroid metabolism disease,"['disorder of steroid metabolic process', 'steroid metabolic process disease', 'steroid metabolism disease', 'disorder of steroid metabolism']",,,,C0268283,,,,,,,,
mondo:0045013,disorder of extraembryonic membrane,"['disease of extraembryonic membrane', 'disorder of extraembryonic membrane', 'extraembryonic membrane disease or disorder']",,,,C3662139,,,,,,,,
mondo:0045014,tetrahydrobiopterin metabolic process disease,"['disorder of tetrahydrobiopterin metabolism', 'disorder of tetrahydrobiopterin metabolic process', 'tetrahydrobiopterin metabolism disease']",,,,C0342676,,,,,,,,
mondo:0045015,carbohydrate transport disease,"['disorder of carbohydrate transport', 'carbohydrate transport disease']",,,,C0268173,,,,,,,,
mondo:0045016,cholesterol catabolic process disease,"['disorder of cholesterol catabolic process', 'cholesterol catabolism disease', 'disorder of cholesterol catabolism']",,,,C0342825,,,,,,,,
mondo:0045017,cholesterol biosynthetic process disease,"['disorder of cholesterol biosynthetic process', 'disorder of cholesterol synthesis', 'cholesterol synthesis disease']",,,,C0342829,,,,,,,,
mondo:0045018,creatine biosynthetic process disease,"['disorder of creatine biosynthetic process', 'creatine synthesis disease', 'disorder of creatine synthesis']",,,,C0574079,,,,,,,,
mondo:0045019,lactation disease,"['disorder of lactation', 'lactation disease']",,,,C0022927,,,,,,,,
mondo:0045020,glycine metabolism disease,"['glycine metabolic process disease', 'glycine metabolism disease', 'disorder of glycine metabolic process', 'disorder of glycine metabolism']",,,,C0268558,,,,,,,,
mondo:0045022,disorder of organic acid metabolism,"['disorder of organic acid metabolic process', 'organic acid metabolic process disease']",,,,,,,,,277.89,,,
mondo:0045023,acquired adrenogenital syndrome,['acquired adrenogenital syndrome'],,,,C0237971,,,,,,,,
mondo:0045024,cancer or benign tumor,"['neoplasm', 'cell proliferation disorder']",,,,,,,,,,,,
mondo:0045030,non-infectious diarrheal disease,"['presumed non-infectious diarrhoea', 'non-infective diarrhoea']",,,,C0267436,,,,,,,,
mondo:0045032,congenital secretory diarrhea,,,,,C0267661,,,,,579.8,,,
mondo:0045033,opportunistic systemic mycosis,,,,,,,,,,,,,
mondo:0045034,infectious disease characteristic,,,,,,,,,,,,,
mondo:0045035,opportunistic infectious,,,,,,,,,,,,,
mondo:0045036,primary infectious,,,,,,,,,,,,,
mondo:0045037,hyalohyphomycosis,,,,,C0343952,,,,D060605,,,,
mondo:0045038,cutaneous basidiobolomycosis,,,,,C0343966,,,,,,,,
mondo:0045039,systemic basidiobolomycosis,,,,,C0343967,,,,,,,,
mondo:0045040,locational disease characteristic,,,,,,,,,,,,,
mondo:0045042,restricted to specific location,['localised'],,,,,,,,,,,,
mondo:0045043,disorder of uterine broad ligament,"['disease of broad ligament of uterus', 'disorder of broad ligament of uterus', 'broad ligament of uterus disease or disorder']",,,,C0404479,,,,,,,,
mondo:0045044,ligament disorder,"['ligament disease or disorder', 'disease of ligament', 'disorder of ligament']",,,,C0263976,,,,,,,,
mondo:0045045,selective IgG immunodeficiency,"['IgG deficiency', 'IgG subclass deficiency', 'selective IgG immunodeficiency']",,,,C0162539,,C27142,,,,,,
mondo:0045046,inherited thyroid metabolism disease,"['rare inborn error of thyroid hormone metabolic process', 'inborn error of thyroid hormone metabolic process']",,,,C0271824,,,,,246.8,,,
mondo:0045047,neurosarcoidosis,['nervous system sarcoidosis'],,,,C0393485,,,,C535814,,,,
mondo:0045048,toxemia of pregnancy,['toxemia of pregnancy'],,,,,,C34943,,,,,,
mondo:0045049,hypermature cataract,,,,,,,,,,366.18,,,
mondo:0045050,nuclear cataract,['lens nucleus cataract (disease)'],,,,,,C135176,,,366.04,,,0100018
mondo:0045051,cortical cataract,['lens cortex cataract (disease)'],,,,,,C135177,,,366.03,,,
mondo:0045052,benign osteogenic neoplasm,"['benign osseous tumor', 'osteogenic neoplasm, benign', 'benign osteogenic tumour', 'benign osteogenic tumor', 'benign osseous tumour', 'benign osteogenic neoplasm', 'benign osseous neoplasm']",,,,,,C6602,,,,,,
mondo:0045053,osteogenic neoplasm,"['osteogenic tumour', 'osseous neoplasm', 'osseous tumour', 'osseous tumor', 'osteogenic neoplasm', 'osteogenic tumor']",,,,,,C6603,,,,,,
mondo:0045054,cancer-related condition,"['cancer related problem/condition', 'problem/condition, cancer-related', 'oncologic complications', 'cancer-related problem or condition', 'problem/condition, cancer related', 'cancer-related condition']",,,,C0280950,,C8278,,,,,,
mondo:0045055,glycogen-rich carcinoma,['Glycogen-rich carcinoma'],0081028,,,,,C4153,,,,,,
mondo:0045056,grade II meningioma,"['grade 2 meningioma', 'grade II meningioma', 'WHO grade II meningioma']",,,,C1512259,,C38937,,,,,,
mondo:0045057,delirium,['OBS syndrome'],,,,C0011206,,C2981,0009267,D003693,293.0,,,
mondo:0045058,ACTH-producing pituitary gland neoplasm,"['adrenocorticotropin secreting pituitary gland tumor', 'ACTH-producing pituitary gland neoplasm', 'ACTH-secreting tumour of pituitary', 'adrenocorticotropin secreting pituitary gland tumour', 'adrenocorticotropin secreting tumor of the pituitary', 'ACTH-secreting tumour of the pituitary', 'adrenocorticotropin secreting neoplasm of the pituitary', 'ACTH-producing pituitary tumor', 'adrenocorticotropin producing pituitary gland tumor', 'ACTH producing pituitary gland neoplasm', 'ACTH-secreting tumor of pituitary', 'ACTH-producing pituitary tumour', 'ACTH-producing pituitary neoplasm', 'corticotropin secreting pituitary gland neoplasm', 'pituitary corticotropin secreting tumour', 'adrenocorticotropin secreting neoplasm of pituitary', 'adrenocorticotropin secreting tumor of pituitary', 'adrenocorticotropin secreting tumour of pituitary', 'pituitary corticotropin secreting neoplasm', 'adrenocorticotropin secreting tumour of the pituitary', 'adrenocorticotropin producing pituitary gland tumour', 'ACTH-secreting tumor of the pituitary', 'pituitary corticotropin secreting tumor']",,,,C0278862,,C7909,,,,,,
mondo:0045059,cribriform carcinoma of breast,"['ductal carcinoma, cribriform type']",5675,,,,,,,,,,,
mondo:0045060,intraductal cribriform breast adenocarcinoma,"['DCIS of the breast with cribriform pattern', 'ductal carcinoma in situ of the breast with cribriform pattern', 'cribriform ductal carcinoma in situ of the breast', 'ductal carcinoma in situ of breast with cribriform pattern', 'non-infiltrating cribriform ductal breast carcinoma', 'cribriform ductal breast carcinoma in situ', 'cribriform DCIS of the breast', 'cribriform DCIS of breast', 'non-invasive cribriform ductal breast carcinoma', 'DCIS of breast with cribriform pattern', 'intraductal cribriform breast adenocarcinoma', 'cribriform ductal carcinoma in situ of breast']",,,,C1334248,,C5138,,,,,,
mondo:0045063,major salivary gland adenoid cystic carcinoma,"['adenoid cystic carcinoma of major salivary gland', 'major salivary gland adenoid cystic cancer', 'major salivary gland adenoid cystic carcinoma', 'adenoid cystic carcinoma of the major salivary gland']",,,,C1334548,,C5905,,,,,,
mondo:0045068,minor salivary gland adenoid cystic carcinoma,"['adenoid cystic carcinoma of minor salivary gland', 'minor salivary gland adenoid cystic carcinoma', 'adenoid cystic carcinoma of the minor salivary gland']",,,,C1334769,,C5936,,,,,,
mondo:0045069,minor salivary gland carcinoma,"['carcinoma of minor salivary gland', 'minor salivary gland cancer', 'minor salivary gland carcinoma', 'carcinoma of the minor salivary gland']",,,,C1334771,,C5957,,,,,,
mondo:0045070,digestive system melanoma,"['gastrointestinal melanoma', 'digestive system melanoma', 'digestive system melanoma (disease)']",,,,C1333798,,C7091,,,,,,
mondo:0045071,mycosis fungoides variant,['mycosis fungoides variant'],,,,C1513782,,C39644,,,,,,
mondo:0045072,ectopic hormone secretion syndrome associated with neoplasia,"['ectopic hormone secretion syndrome associated with neoplasia', 'neoplasm associated ectopic hormone secretion syndrome']",,,,C0851689,,C4065,,,,,,
mondo:0049221,"myopia 26, X-linked, female-limited","['MYP26', 'myopia 26, X-linked, female-limited']",,301010,,C4538795,"['-0.04196', '0.0341', '-0.001997', '-0.02913', '0.01252', '-0.07086', '-0.01342', '0.06122', '-0.05542', '-0.0562', '-0.02551', '-0.007385', '0.004784', '-0.00749', '-0.003767', '-0.01942', '0.01682', '-0.00426', '-0.0182', '-0.09076', '-0.03302', '-0.001001', '0.01533', '-0.02191', '0.02502', '-0.007114', '-0.01374', '-0.006058', '0.01724', '-0.05765', '0.04788', '4.613e-05', '0.08154', '0.02573', '-0.00881', '-0.03748', '-0.01929', '-0.0559', '-0.032', '-0.05853', '0.03036', '-0.05255', '0.002401', '-0.03604', '-0.01452', '-0.05438', '-0.004387', '0.0179', '-0.002254', '0.02008', '-0.00823', '-0.01444', '-0.000423', '-0.00631', '-0.02116', '-0.02972', '0.07007', '-0.02592', '-0.0624', '0.0104', '0.043', '0.008385', '0.011635', '0.02979', '-0.01217', '0.00209', '0.064', '0.04575', '-0.0494', '0.05295', '-0.03284', '0.008224', '0.008354', '-0.04047', '0.05676', '0.006657', '0.01782', '-0.00618', '-0.0356', '-0.01689', '-0.00639', '-0.01069', '0.00285', '0.0631', '-0.01765', '0.0268', '0.01958', '0.05673', '0.0672', '0.01116', '0.01413', '0.06445', '-0.001033', '0.02197', '0.127', '0.02425', '0.04276', '-0.0583', '-0.00797', '0.0305']",,,,,,,
mondo:0049222,"intellectual disability, X-linked 107","['mental retardation, X-linked 107', 'MRX107', 'intellectual developmental disorder, X-linked 107', 'intellectual disability, X-linked 107']",0112054,301013,,,,,,,,,,
mondo:0049223,"osteogenesis imperfecta, type 19","['osteogenesis imperfecta, type XIX, X-linked recessive', 'osteogenesis imperfecta, type XIX', 'OI19']",0111847,301014,,CN252653,,,,,,,,
mondo:0054549,peroxisome biogenesis disorder 10B,"['peroxisome biogenesis disorder 10B', 'PBD10B']",,617370,,,,,,,,,,
mondo:0054550,"avascular necrosis of femoral head, primary, 1","['ischemic necrosis of femoral head', 'osteonecrosis of femoral head', 'femoral head, aseptic necrosis of', 'ischaemic necrosis of femoral head', 'avascular necrosis of femoral head, primary, 1', 'ANFH1', 'Femoral head, avascular necrosis of', 'avascular necrosis of the femoral head']",,608805,,,,,,,,,,
mondo:0054551,"avascular necrosis of femoral head, primary, 2","['ANFH2', 'avascular necrosis of femoral head, primary, 2']",,617383,,,,,,,,,,
mondo:0054559,"congenital disorder of glycosylation, type IIq","['COG2-CDG', 'CDG2Q', 'CDG Iiq', 'COG2-related congenital disorder of glycosylation']",0070269,617395,435934,C4479353,"['-0.05795', '0.04422', '0.02495', '0.00931', '0.0435', '-0.1091', '0.00899', '0.0655', '-0.1139', '-0.03156', '-0.03082', '-0.02303', '0.00623', '0.02408', '-0.0778', '-0.03513', '0.02718', '-0.0436', '-0.04315', '-0.1915', '-0.02036', '-0.02614', '0.1019', '-0.03223', '0.04346', '-0.02245', '-0.01727', '-0.03265', '0.04645', '-0.0709', '0.0887', '0.02457', '0.10565', '0.0694', '-0.009094', '-0.03018', '-0.035', '-0.04218', '-0.01389', '-0.1032', '0.04282', '-0.09076', '0.008606', '0.002146', '-0.01516', '-0.0865', '-0.02115', '0.0935', '0.0642', '0.04037', '-0.0415', '-0.02202', '0.02078', '-0.00566', '-0.07684', '-0.04648', '0.0684', '-0.0004208', '-0.10626', '0.00059', '0.04626', '0.02379', '0.0394', '-0.002558', '-0.005753', '0.01235', '0.0937', '0.0702', '-0.11847', '0.06934', '-0.07275', '0.04947', '0.01556', '-0.06805', '0.04984', '0.0449', '0.01712', '-0.00893', '-0.08', '-0.02246', '-0.00336', '-0.006344', '-0.03638', '0.0812', '0.002865', '-0.004776', '0.0292', '0.091', '0.10803', '0.003544', '0.03397', '0.10846', '0.0115', '0.03008', '0.1516', '0.0684', '0.10443', '-0.1426', '0.00823', '0.0605']",,,,,,,
mondo:0054560,anauxetic dysplasia 1,"['spondylometaepiphyseal dysplasia, Menger type', 'ANXD1', 'anauxetic dysplasia 1', 'spondyloepimetaphyseal dysplasia, anauxetic type', 'anauxetic dysplasia', 'spondylometaepiphyseal dysplasia, anauxetic type']",,607095,,,,,,,,,,
mondo:0054561,anauxetic dysplasia 2,"['ANXD2', 'anauxetic dysplasia 2']",0080962,617396,,,,,,,,,,
mondo:0054565,short-rib thoracic dysplasia 17 with or without polydactyly,"['SRTD17', 'short-rib thoracic dysplasia 17 with or without POLYDACTYLY']",,617405,,,"['-0.03525', '0.03955', '0.00902', '-0.02939', '0.02611', '-0.0422', '0.01161', '0.0663', '-0.05185', '-0.03952', '-0.0334', '-0.01238', '0.002867', '0.0054', '-0.0407', '-0.01964', '0.003855', '-0.0444', '-0.02075', '-0.0954', '-0.003126', '-0.001072', '0.06555', '-0.01915', '0.00819', '-0.01114', '-0.01752', '-0.007904', '0.01087', '-0.03387', '0.03983', '-0.01366', '0.0559', '0.02034', '0.02895', '-0.02492', '-0.00799', '-0.02242', '-0.006863', '-0.04727', '0.02223', '-0.05704', '0.01955', '-0.01538', '-0.00395', '-0.034', '-0.015114', '0.04648', '0.007565', '0.01383', '-0.01833', '-0.008736', '0.02124', '0.004276', '-0.02902', '-0.04047', '0.03009', '-0.03836', '-0.06635', '0.0003746', '0.03888', '0.02728', '-0.01262', '0.006207', '-0.006992', '0.001771', '0.05438', '0.03958', '-0.04526', '0.0708', '-0.05225', '0.02177', '0.0255', '-0.0377', '0.0097', '0.03204', '-0.005154', '-0.01255', '-0.03458', '-0.03464', '-0.01295', '0.01536', '-0.000693', '0.03592', '-0.0146', '-0.007137', '0.01967', '0.06125', '0.0518', '0.005356', '-0.00761', '0.04062', '-0.004143', '0.0273', '0.1054', '0.01473', '0.0576', '-0.081', '0.009026', '0.0248']",,,,,,,
mondo:0054573,Lopes-Maciel-Rodan syndrome,"['Lopes-Maciel-Rodan syndrome', 'LOMARS']",,617435,,C4479491,,,,,,,,
mondo:0054577,"bleeding disorder, platelet-type, 21","['bleeding disorder, platelet-type, 21', 'BDPLT21']",,617443,,,,,,,,,,
mondo:0054581,Townes-Brocks syndrome 1,"['renal-ear-anal-radial syndrome', 'Townes-Brocks syndrome 1', 'rear syndrome', 'deafness, sensorineural, with imperforate anus and thumb anomalies', 'Townes-Brocks-branchiootorenal-like syndrome', 'townes-brocks branchiootorenal-like syndrome', 'anus, imperforate, with hand, Foot, and Ear anomalies', 'TBS1']",,107480,,,,,,,,,,
mondo:0054582,Townes-Brocks syndrome 2,"['Townes-Brocks syndrome 2', 'TBS2']",,617466,,,,,,,,,,
mondo:0054588,Noonan syndrome-like disorder with loose anagen hair 2,"['Noonan syndrome-like disorder with loose anagen hair 2', 'NSLH2']",0080693,617506,,,,C176940,,,,,,
mondo:0054591,Stankiewicz-Isidor syndrome,"['STISS', 'Stankiewicz-Isidor syndrome']",,617516,,C4479599,"['-0.0116', '0.03726', '-0.00633', '-0.0101', '0.01118', '-0.0577', '-0.01346', '0.05182', '-0.0452', '-0.0326', '0.001431', '-0.013', '0.01591', '0.02142', '-0.01927', '-0.0372', '0.00925', '-0.01485', '-0.006725', '-0.07135', '-0.008835', '-0.02817', '0.0313', '-0.0294', '0.016', '0.00531', '-0.02736', '-0.001451', '0.03038', '-0.02617', '0.04724', '-0.01503', '0.05084', '0.03397', '0.00418', '-0.02998', '-0.0248', '-0.01173', '-0.0022', '-0.05725', '0.00635', '-0.03793', '0.02252', '-0.0294', '0.0004487', '-0.04248', '-0.04962', '0.0273', '0.01706', '0.01399', '-0.004425', '-0.009315', '0.0183', '-0.00948', '-0.0436', '-0.00804', '0.029', '-0.004494', '-0.0562', '0.004837', '0.03632', '0.0318', '0.006935', '0.02435', '0.00607', '0.015396', '0.05185', '0.01591', '-0.04633', '0.0655', '-0.066', '0.014175', '0.0141', '-0.0257', '0.02818', '0.02032', '0.000377', '0.00714', '-0.0373', '-0.03256', '0.000934', '0.00799', '-0.03195', '0.05493', '-0.01295', '-0.01007', '0.004658', '0.0567', '0.0604', '0.003588', '0.02051', '0.05258', '-0.00742', '-0.00524', '0.09393', '0.02171', '0.02588', '-0.09863', '-0.009476', '0.01926']",,,,,,,
mondo:0054593,"microcephaly 18, primary, autosomal dominant","['primary autosomal dominant microcephaly 18', 'MCPH18', 'microcephaly 18, primary, autosomal dominant']",0070295,617520,,C4479608,,,,,,,,
mondo:0054601,"pituitary adenoma 5, multiple types","['PITA5', 'pituitary adenoma 5, multiple types']",0112008,617540,,C4539685,,,,,,,,
mondo:0054602,"gaze palsy, familial horizontal, with progressive scoliosis, 2","['HGPPS2', 'gaze palsy, familial horizontal, with progressive scoliosis, 2']",,617542,,C4479640,,,,,,,,
mondo:0021115,luminal B breast carcinoma,"['Luminal B breast carcinoma', 'Luminal B subtype of breast carcinoma', 'Luminal B', 'Luminal B oestrogen receptor positive subtype of breast carcinoma', 'Luminal B breast cancer', 'Luminal B estrogen receptor positive subtype of breast carcinoma']",0080674,,,C3642346,,C53555,,,,,,
mondo:0021116,luminal A breast carcinoma,"['Luminal A oestrogen receptor positive subtype of breast carcinoma', 'Luminal A subtype of breast carcinoma', 'Luminal A estrogen receptor positive subtype of breast carcinoma', 'Luminal A breast carcinoma', 'Luminal A', 'Luminal A breast cancer']",,,,C3642345,,C53554,,,,,,
mondo:0021117,lung neoplasm,"['tumour of the lung', 'neoplasm of lung', 'lung neoplasm', 'neoplasms, pulmonary', 'lung neoplasm (disease)', 'tumor of the lung', 'neoplasm, lung', 'lung', 'neoplasm of the lung', 'lung tumour', 'tumor of lung', 'neoplasms, lung', 'lung neoplasms', 'tumour of lung', 'neoplasm, pulmonary', 'lung tumor']",,,,,,C3200,,D008175,,,,
mondo:0021118,intestinal neoplasm,"['intestinal tumor', 'intestinal benign neoplasm', 'intestine tumour', 'intestinal tumours', 'intestine neoplasm (disease)', 'tumor of intestines', 'intestinal tumors', 'bowel neoplasm', 'neoplasm of intestine', 'intestine tumor', 'tumour of intestine', 'tumour of the intestines', 'neoplasm of intestines', 'neoplasm of intestinal tract', 'tumour of intestines', 'intestinal neoplasms', 'intestine growth', 'intestinal neoplasm', 'neoplasm of the intestines', 'tumor of the intestines', 'intestinal tumour', 'tumor of intestine']",4610,,,,,C3141,,,,,,
mondo:0021119,non-functioning endocrine neoplasm,"['nonfunctioning tumour', 'endocrine-inactive tumour', 'endocrine-inactive tumor', 'non-functioning endocrine neoplasm', 'nonfunctional Endocrine neoplasm', 'nonfunctioning tumor']",,,,C2986656,,C94760,,,,,,
mondo:0021120,functioning endocrine neoplasm,"['functioning tumour', 'functioning tumor', 'functioning endocrine neoplasm']",,,,C2986655,,C94759,,,,,,
mondo:0021121,hemangioendothelioma,"['angioendothelioma', 'hemangioendothelioma']",,,,C0018915,,C3084,,D006390,,,,
mondo:0021123,Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone,"['Ewing sarcoma/peripheral primitive neuroectodermal tumor of bone', 'Ewing^s sarcoma/peripheral primitive neuroectodermal tumour of bone', 'bone tissue Ewing sarcoma/peripheral primitive neuroectodermal tumour', 'bone tissue Ewing sarcoma/peripheral primitive neuroectodermal tumor', 'Ewing^s sarcoma/peripheral primitive neuroectodermal tumor of bone']",,,,C1333481,,C35871,,,,,,
mondo:0021124,female infertility,"['female sterility', 'female sub-fertility', 'infertility disorder of female reproductive system', 'subfertility, female', 'sterility, postpartum', 'female infertility', 'sub fertility, female', 'sub-fertility, female', 'female reproductive system infertility disorder', 'sterility, female', 'female reproductive system infertility', 'postpartum sterility', 'female subfertility']",,,,C0341869,,,0008560,D007247,628.9,N97,,
mondo:0021125,disease characteristic,"['modifier', 'qualifier']",,,,,,C41009,,,,,,
mondo:0021126,syndromic or isolated,,,,,,,,,,,,,
mondo:0021127,has a syndromic presentation,,,,,,,,,,,,,
mondo:0021128,has an isolated presentation,,,,,,,,,,,,,
mondo:0021129,microphthalmia,"['microphthalmos', 'nanophthalmos', 'microphthalmia', 'simple microphthalmos']",10629,,,,"['-0.1731', '-0.00469', '0.0823', '-0.01855', '0.1613', '0.04514', '-0.0705', '0.1646', '-0.1366', '-0.234', '-0.01775', '-0.1484', '-0.10974', '0.1882', '-0.2361', '-0.129', '0.04208', '-0.11194', '-0.16', '-0.4468', '0.0941', '-0.01744', '0.1836', '-0.07654', '0.1808', '0.03333', '-0.0591', '0.03192', '0.2017', '0.02153', '0.21', '-0.0416', '0.1499', '0.1932', '0.0989', '0.01416', '0.11707', '-0.03308', '-0.02216', '-0.1428', '0.2001', '-0.1334', '-0.03436', '-0.1664', '-0.0586', '-0.2676', '0.1135', '0.1907', '0.177', '0.0976', '-0.0963', '-0.03912', '-0.00414', '-0.1241', '-0.1654', '-0.10736', '0.2477', '0.0783', '-0.305', '0.0343', '-0.04993', '-0.04904', '-0.000761', '0.02371', '-0.11145', '-0.0725', '0.25', '0.3816', '-0.2644', '0.1669', '-0.1451', '0.1794', '0.05576', '-0.1919', '0.03226', '-0.03677', '0.1461', '-0.01482', '-0.1296', '-0.10345', '-0.03503', '0.01494', '0.02449', '0.2837', '-0.1594', '-0.3494', '0.07263', '0.2825', '0.0911', '0.2021', '0.012726', '0.3232', '0.1559', '0.1001', '0.4873', '-0.0633', '0.2793', '-0.1641', '-0.0407', '0.1075']",C98989,0005569,D008850,743.11,,,0000568
mondo:0021130,disorder of sphingolipid biosynthesis,"['inborn error of sphingolipid biosynthetic process', 'rare inborn error of sphingolipid biosynthetic process']",,,,,,,,,,,,
mondo:0021131,frontal lobe ependymal tumor,"['ependymal tumor of frontal lobe', 'ependymal tumour of frontal lobe', 'frontal lobe ependymal tumor']",,,,C4330009,,C131573,,,,,,
mondo:0021132,tertiary hyperparathyroidism,['tertiary hyperparathyroidism'],,,,C0271858,,C114821,,,588.89,,,
mondo:0021133,acquired factor XIII deficiency,"['aFXIII', 'acquired factor XIII deficiency']",,,599513,C0238120,,C131629,,,,,,
mondo:0021134,acquired factor X deficiency,"['acquired factor X deficiency', 'aFX']",,,599501,C0272328,,C131626,,,286.9,,,
mondo:0021135,rare or common,,,,,,,,,,,,,
mondo:0021136,rare,,,,,,,,,,,,,
mondo:0021137,not rare,,,,,,,,,,,,,
mondo:0021138,bone marrow cancer,"['bone marrow cancer', 'malignant bone marrow tumour', 'malignant neoplasm of bone marrow', 'malignant bone marrow neoplasm', 'cancer of bone marrow', 'malignant bone marrow tumor']",,,,C2703042,,C35501,,,,,,
mondo:0021139,congenital or acquired,,,,,,,,,,,,,
mondo:0021140,congenital,,,,,,,,,,,,,
mondo:0021141,acquired,['not genetically inherited'],,,409941,,,,,,,,,
mondo:0021142,acquired rippling muscle disease,"['sporadic rippling muscle disease', 'acquired rippling muscle disease']",,,,,,,,,,,,
mondo:0021143,melanocytic neoplasm,"['melanocytic neoplasm', 'melanomas and nevi']",,,,C1302746,,C7058,,D018326,,,,
mondo:0021144,ovarian clear cell tumor,"['ovarian clear cell neoplasm', 'ovarian clear cell tumor', 'clear cell ovarian cancer']",,,,C0346164,,C40076,,,,,,
mondo:0021146,headache disorder,"['chronic headache', 'headaches, chronic', 'headache syndromes', 'cephalgia syndrome', 'headache syndrome', 'daily headache, chronic', 'syndrome, headache', 'headaches, chronic daily', 'headache disorder', 'headache, chronic daily', 'intractable headache', 'intractable headaches', 'daily headaches, chronic', 'headache, intractable', 'chronic daily headache', 'headache, chronic', 'chronic daily headaches', 'cephalgia syndromes', 'chronic headaches', 'headaches, intractable']",,,,,,,,D020773,,,,
mondo:0021147,disorder of development or morphogenesis,,,,,,,,,,,Q00-Q99,,
mondo:0021148,female reproductive system neoplasm,"['female reproductive system tumor', 'neoplasm of female reproductive system', 'female reproductive system neoplasm (disease)', 'female reproductive system neoplasm', 'female reproductive organ tumour', 'female reproductive system tumour', 'gynecologic tumour', 'tumour of the female reproductive system', 'gynecologic neoplasm', 'tumor of the female reproductive system', 'gynecologic tumor', 'tumour of female reproductive system', 'neoplasm of female reproductive organ', 'female reproductive organ tumor', 'female reproductive organ neoplasm (disease)', 'tumor of female reproductive system', 'neoplasm of the female reproductive system']",,,,C0017416,,C3053,1001331,D005833,,,,
mondo:0021149,hereditary vs non-hereditary etiology,,,,,,,,,,,,,
mondo:0021151,non-genetic,,,,,,,,,,,,,
mondo:0021152,inherited,,,,,,,,0004420,,,,,
mondo:0021154,dermis disorder,"['dermis disease', 'other dermis disorder', 'dermis disease or disorder', 'disease of dermis', 'disorder of dermis']",,,79381,CN227618,,,,,,,,
mondo:0021155,X-linked cone-rod dystrophy,"['cone-rod dystrophy, X-linked']",,,,,,,,,,,,
mondo:0021156,hypophysitis,"['hypophysitides', 'pituitary', 'pituitary gland', 'hypophysis cerebri', 'pituitary gland inflammation', 'hypophysis', 'gland, pituitary', 'nervous system, pituitary']",,,,C0342409,,C12399,,D000072659,,,,
mondo:0021157,gonococcal cervicitis,"['gonorrhea of uterine cervix', 'gonorrhoea of cervix', 'gonorrhea of cervix', 'gonorrhoea of uterine cervix']",,,,C0812378,,,,,,,,
mondo:0021158,gonococcal epididymo-orchitis,,,,,C0341782,,,,,,,,
mondo:0021159,gonococcal salpingitis,['Neisseria gonorrhoeae caused salpingitis'],,,,C0341811,,,,,,,,
mondo:0021160,gonococcal cystitis,['Neisseria gonorrhoeae caused cystitis'],,,,C0473230,,,,,,,,
mondo:0021161,gonococcal prostatitis,['Neisseria gonorrhoeae caused prostatitis (disease)'],,,,C0341755,,,,,,,,
mondo:0021162,carotenemia,"['hypercarotinemia', 'acquired carotenemia']",9969,,,C0154271,,,,,278.3,,,
mondo:0021163,kidney neoplasm,"['renal tumor', 'neoplasm of kidney', 'kidney tumour', 'kidney neoplasm', 'tumor of kidney', 'renal tumour', 'kidney neoplasm (disease)', 'renal tumours', 'neoplasm of the kidney', 'kidney tumor', 'renal neoplasm', 'tumour of kidney', 'tumor of the kidney', 'tumour of the kidney', 'renal tumors']",,,,,,C3150,,,239.5,,,
mondo:0021164,posthitis,['prepuce of penis inflammation'],,,,C0235640,,,,,,,,
mondo:0021165,Paget disease,"['Paget cell neoplasm', 'Paget^s disease', 'Paget disease', 'Paget^s cell neoplasm']",,,,,,C7073,,,,,,
mondo:0021166,inflammatory disease,['anatomical structure inflammation'],,,,C1290884,,C93210,,,799.89,,,
mondo:0021167,myositis disease,"['inflammatory disorder of muscle', 'muscle tissue inflammation']",633,,,,,C27578,0000783,D009220,728.9,,,
mondo:0021168,hibernoma,"['Brown fat tumor', 'Brown fat tumour', 'fetal fat cell lipoma', 'hibernoma', 'foetal fat cell lipoma', 'hibernoma, benign', 'Brown fat neoplasm']",,,,C0205822,,C3702,,,,,,
mondo:0021169,epithelioid hemangioma,"['histiocytoid hemangioma', 'epithelioid hemangioma', 'epithelioid haemangioma']",474,,,C0205788,,C4298,,,,,,
mondo:0021171,"Timothy syndrome, classic type",['Timothy syndrome type 1 (disorder)'],,,,,,,,,759.89,,,
mondo:0021172,"Timothy syndrome, atypical type","['ATS', 'Atypical LQT8', 'Timothy syndrome type 2 (disorder)', 'atypical Timothy syndrome']",,,595109,C4304347,,,,,,I49.8,,
mondo:0021175,herpetic vulvovaginitis,"['herpetic vulvovaginitis', 'Herpetic vulvovaginitis', 'Herpetic Vulvovaginitis']",,,,C0019386,,C34697,,,054.11,,,
mondo:0021176,autoimmune hepatitis type 2,['type 2 AIH'],,,563581,C4303163,,,,,,,,
mondo:0021177,autoimmune hepatitis type 3,,,,,C4303162,,,,,,,,
mondo:0021178,injury,"['injury', 'trauma', 'traumatic injury', 'wound']",,,,,,C3671,0000546,D014947,,,,
mondo:0021179,proteostasis deficiencies,"['Proteostasis deficiency', 'disorders, Protein folding', 'Protein Misfolding disorders', 'Protein folding diseases', 'folding disease, Protein', 'Proteostasis dysfunctions', 'disorder, Protein Misfolding', 'dysfunctions, Proteostasis', 'Misfolding diseases, Protein', 'folding diseases, Protein', 'Proteostasis dysfunction', 'Misfolding disease, Protein', 'Misfolding disorders, Protein', 'disorder, Protein folding', 'Misfolding disorder, Protein', 'Protein folding disorders', 'dysfunction, Proteostasis', 'folding disorder, Protein', 'disorders, Protein Misfolding', 'deficiency, Proteostasis', 'proteopathic disease', 'Protein Misfolding disease', 'proteinopathy', 'Protein folding disorder', 'disease, Protein folding', 'diseases, Protein Misfolding', 'Protein Misfolding disorder', 'proteopathy', 'diseases, Protein folding', 'folding disorders, Protein', 'Protein folding disease', 'deficiencies, Proteostasis', 'disease, Protein Misfolding', 'Protein Misfolding diseases']",,,,C2718001,,,,D057165,,,,
mondo:0021180,acquired xanthinuria,['acquired xanthinuria'],,,,,,,,,,,,
mondo:0021181,inherited blood coagulation disorder,"['hereditary coagulation disorders', 'inherited coagulation disorder', 'coagulation disorders, inherited', 'hereditary blood coagulation disorders', 'inherited blood coagulation disorders', 'inherited coagulation disorders', 'coagulation disorder, inherited', 'hereditary blood coagulation disease', 'rare genetic coagulation disorder', 'hereditary coagulation disorder', 'inherited blood coagulation disease', 'coagulation disorder, hereditary', 'coagulation disorders, hereditary']",2214,,183654,CN226819,,,,D025861,,,,
mondo:0021183,HTLV-2 infection,"['Human T lymphotropic Virus 2 Infections', 'Human T-lymphotropic Virus 2 Infection', 'HTLV-II Infections', 'HTLV II INFECT', 'Human T-lymphotropic virus 2 infection', 'Human T lymphotropic Virus 2 Infection', 'Human T-lymphotropic Virus 2 Infections', 'HTLV-II Infection', 'Infection, HTLV-II', 'HTLV-II infection', 'HTLV-2 infection', 'Infections, HTLV II', 'Infections, HTLV-II', 'INFECT HTLV II']",,,,C0020102,,,1001349,D015491,,,,
mondo:0021184,deltaretrovirus infections,"['HTLV BLV infections', 'HTLV infections', 'BLV infection', 'HTLV-BLV infections', 'HTLV-BLV infection', 'infection, Deltaretrovirus', 'HTLV infection', 'Deltaretrovirus infection', 'BLV infections', 'infections, Deltaretrovirus']",,,,,,,,D006800,,,,
mondo:0021187,hyperlipidemia,"['lipidemias', 'lipidemia', 'hyperlipidemia (disease)', 'hyperlipemia', 'hyperlipemias', 'hyperlipidemia', 'lipemia', 'lipemias']",,,,CN236649,"['-0.1455', '0.1526', '0.002337', '-0.04465', '0.0276', '-0.05838', '-0.05252', '0.1903', '-0.1339', '0.01921', '-0.05704', '-0.03766', '0.06165', '0.05', '-0.0982', '-0.0965', '-0.01848', '0.02728', '-0.09186', '-0.2563', '0.00753', '-0.1694', '0.0872', '0.01106', '0.1031', '-0.00799', '0.07367', '-0.0087', '-0.1031', '-0.1099', '0.2024', '0.02464', '0.1981', '0.02682', '-0.0445', '-0.014755', '-0.04962', '-0.00653', '0.0402', '-0.2239', '0.007202', '-0.1506', '0.11285', '-0.0872', '-0.06238', '-0.1201', '0.03467', '0.0749', '0.00531', '0.0744', '-0.04202', '-0.0008545', '0.1031', '-0.03278', '-0.0586', '-0.0005817', '0.1543', '-0.1743', '-0.2257', '0.0001694', '0.04523', '0.0889', '0.0702', '-0.075', '-0.0312', '-0.01982', '0.155', '0.0878', '-0.1968', '0.0473', '-0.11176', '0.0476', '0.0292', '-0.04504', '0.0831', '0.06088', '0.0618', '0.01193', '-0.05222', '-0.05563', '-0.0324', '0.006542', '-0.02455', '0.08606', '0.01522', '0.0939', '0.03897', '0.05432', '0.1802', '0.03143', '0.1027', '0.1448', '-0.1276', '0.00234', '0.2612', '0.1565', '0.0724', '-0.1414', '-0.1334', '0.03084']",,0003774,D006949,272.4,E78.5,,0003077
mondo:0021189,intestinal motility disease,['disorder of intestinal motility'],,,,,,,,,,,,
mondo:0021190,DNA repair disease,"['DNA Repairs, deficient', 'DNA repair-deficiencies', 'repair, deficient DNA', 'DNA repair deficiency disorders', 'DNA repair-deficiency disorder', 'deficient DNA Repairs', 'DNA repair-deficiency', 'disorders, DNA repair-deficiency', 'syndrome, chromosome instability', 'syndromes, chromosome instability', 'chromosome instability syndromes', 'Repairs, deficient DNA', 'deficient DNA repair', 'disorder, DNA repair-deficiency', 'DNA repair, deficient', 'DNA repair deficiency', 'chromosome instability syndrome', 'disorder of DNA repair']",,,,,,C7757,0008499,D049914,,,,
mondo:0021192,odontogenic neoplasm,"['tumour of calcareous tooth', 'neoplasm of calcareous tooth', 'odontogenic tumor', 'calcareous tooth tumour', 'tumor of calcareous tooth', 'calcareous tooth neoplasm (disease)', 'odontogenic tumour', 'calcareous tooth tumor', 'odontogenic neoplasm']",,,,C0028880,,C3286,,D009808,,,,
mondo:0021193,neuroepithelial neoplasm,"['primary neuroepithelial tumor', 'tumor of neuroepithelial tissue', 'neuroepithelial tumours', 'neuroepithelial neoplasm', 'tumour of the neuroepithelium', 'primary neuroepithelial tumour', 'tumor of the neuroepithelium', 'neuroepithelial tissue tumour', 'neuroepithelial tissue tumor', 'neuroepithelial tissue neoplasm', 'neoplasm of the neuroepithelium', 'neuroepithelial tumors', 'tumour of neuroepithelium', 'tumour of neuroepithelial tissue', 'neoplasm of neuroepithelium', 'neuroepithelial tumor', 'tumor of neuroepithelium', 'neuroepithelial neoplasms', 'neuroepithelial tumour', 'neoplasm of neuroepithelial tissue']",,,,,,C3787,,D018302,,,,
mondo:0021201,skin infection,['skin infection'],,,,C0037278,,C35025,,,,,,
mondo:0021202,allergic otitis media,['allergic form of otitis media (disease)'],,,,C0271447,,,,,,,,
mondo:0021203,serous otitis media,"['otitis media with effusion', 'SOM', 'secretory otitis media']",,,,,,,,,,,,
mondo:0021204,chronic otitis media,"['otitis media (disease), chronic']",,,,C0271441,,,,,381.3,,,
mondo:0021205,disorder of ear,"['Ear disease', 'ear disease', 'Ear disorder', 'disorder of ear', 'ear disease or disorder', 'disease of ear']",,,,C0013447,,C26757,,,388.9,,,
mondo:0021206,chronic non-suppurative otitis media,"['non-suppurative otitis media, chronic']",,,,C0395869,,,,,381.3,,,
mondo:0021207,Crohn jejunitis,,,,,C0267379,,,,,,,,
mondo:0021208,endocrine alopecia,,,,,C0002176,,,,,704.09,,,
mondo:0021209,heart neoplasm,"['heart tumor', 'Cardiac tumor', 'neoplasm of the heart', 'Intracavitary tumours', 'heart tumour', 'primary cardiac tumors, childhood', 'myocardial tumors (rhabdomyomas and fibromas)', 'neoplasm of heart', 'Cardiac tumour', 'tumor of heart', 'tumor of the heart', 'tumour of heart', 'Intracavitary tumors', 'Cardiac neoplasms', 'myocardial tumours (rhabdomyomas and fibromas)', 'heart neoplasm (disease)', 'tumour of the heart', 'Cardiac neoplasm']",,,,,,C3081,1001339,,,,,
mondo:0021210,trachea neoplasm,"['trachea neoplasm (disease)', 'tracheal tumor', 'tracheal tumour', 'tumour of trachea', 'neoplasm of trachea', 'trachea tumor', 'tumour of the trachea', 'trachea tumour', 'neoplasm of the trachea', 'tumor of trachea', 'tumor of the trachea', 'tracheal neoplasm']",,,,C0040582,,C3419,1001437,D014134,,,,0100551
mondo:0021211,brain neoplasm,"['tumor of brain', 'brain tumor', 'neoplasm of the brain', 'tumour of the Brain', 'tumor of the Brain', 'tumour of brain', 'brain tumour', 'neoplasm of brain', 'brain neoplasms', 'brain neoplasm (disease)']",,,,,,C2907,,,,,,
mondo:0021218,placenta neoplasm,"['placental tumours', 'placenta tumours', 'placenta neoplasms', 'placental neoplasm', 'trophoblastic tumour placental site', 'tumour of the placenta', 'placental tumour', 'placenta neoplasm (disease)', 'neoplasm of placenta', 'tumour of placenta', 'placenta tumour', 'neoplasm of the placenta', 'placental tumors', 'tumor of placenta', 'tumor of the placenta', 'placental tumor', 'trophoblastic tumor placental site', 'placenta tumor', 'placenta tumors']",,,,,,C4858,,,,,,
mondo:0021220,eye neoplasm,"['eyeball of camera-type eye tumor', 'ocular tumour', 'ocular neoplasm', 'tumour of eye', 'neoplasm of eye', 'tumor of eye', 'neoplasm of eyeball of camera-type eye', 'eye neoplasm (disease)', 'eyeball of camera-type eye tumour', 'eye tumor', 'ocular tumor', 'neoplasm of the eye', 'tumour of eyeball of camera-type eye', 'tumour of the eye', 'tumor of eyeball of camera-type eye', 'tumor of the eye', 'eye tumour']",,,,,,C3030,,,,C69-C72,,
mondo:0021221,vestibulocochlear nerve neoplasm,"['eighth cranial nerve tumor', 'neoplasm of the acoustic nerve', 'vestibulocochlear nerve neoplasm (disease)', 'tumor of the acoustic nerve', 'tumor of acoustic nerve', 'eighth cranial nerve neoplasms', 'neoplasm of acoustic nerve', 'eighth cranial nerve tumour', 'tumor of eighth cranial nerve', 'tumour of vestibulocochlear nerve', 'tumor of the eighth cranial nerve', 'eighth cranial nerve neoplasm', 'vestibulocochlear nerve neoplasms', 'cranial nerve eight neoplasms', 'acoustic nerve tumour', 'tumour of the vestibulocochlear nerve', 'neoplasm of vestibulocochlear nerve', 'vestibulocochlear nerve tumor', 'neoplasm of the vestibulocochlear nerve', 'vestibulocochlear nerve tumour', 'acoustic nerve neoplasm', 'neoplasm of the eighth cranial nerve', 'tumor of the vestibulocochlear nerve', 'tumour of acoustic nerve', 'tumor of vestibulocochlear nerve', 'acoustic nerve tumor', 'tumour of the eighth cranial nerve', 'neoplasm of eighth cranial nerve', 'tumour of eighth cranial nerve', 'tumour of the acoustic nerve', 'Vestibuloacoustic nerve neoplasms']",,,,C0346330,,C5120,,,,,,
mondo:0021222,lacrimal gland neoplasm,"['lacrimal gland tumour', 'neoplasm of lacrimal gland', 'tumor of the lacrimal gland', 'neoplasm of the lacrimal gland', 'lacrimal gland tumor', 'tumour of the lacrimal gland', 'tumour of lacrimal gland', 'lacrimal gland neoplasm (disease)', 'tumor of lacrimal gland']",,,,,,C4360,,,,,,
mondo:0021223,digestive system neoplasm,"['neoplasm of the GI system', 'neoplasm of gastrointestinal system', 'digestive tumor', 'neoplasm of digestive system', 'GI tumour', 'tumor of gastrointestinal system', 'neoplasm of GI system', 'gastrointestinal tumor', 'tumour of the gastrointestinal system', 'tumor of the GI system', 'gastrointestinal neoplasm', 'gastrointestinal system tumor', 'digestive system neoplasm (disease)', 'digestive tumour', 'GI system tumor', 'tumor of the digestive system', 'tumor of the gastrointestinal system', 'tumor of GI system', 'gastrointestinal system tumour', 'neoplasm of the digestive system', 'tumour of the GI system', 'gastrointestinal tumour', 'tumor of digestive system', 'digestive neoplasm', 'gastrointestinal system neoplasm', 'tumour of digestive system', 'GI system neoplasm', 'digestive system tumor', 'neoplasm of the gastrointestinal system', 'tumour of gastrointestinal system', 'digestive system tumour', 'GI system tumour', 'GI tumor', 'tumour of GI system', 'GI neoplasm', 'tumour of the digestive system']",,,,,,C3052,0008549,D005770,,,,
mondo:0021224,iris neoplasm,"['tumor of iris', 'iris neoplasm (disease)', 'tumour of iris', 'neoplasm of iris', 'iris tumour', 'tumor of the iris', 'tumour of the iris', 'neoplasm of the iris', 'iris tumor']",,,,C0022079,,C3142,,D015811,,,,
mondo:0021225,uvea neoplasm,"['uvea neoplasm (disease)', 'uveal neoplasm', 'tumor of uvea', 'tumor of the uvea', 'neoplasm of the uvea', 'uvea tumour', 'neoplasm of uvea', 'uveal tumor', 'tumour of the uvea', 'uvea tumor', 'uveal tumour', 'tumour of uvea']",,,,C0042162,,C3436,,,,,,
mondo:0021227,adrenal gland neoplasm,"['adrenal tumor', 'adrenal tumour', 'adrenal/paraganglial tumour', 'ADRENALGLAND', 'adrenal neoplasm', 'neoplasm of adrenal gland', 'tumor of adrenal gland', 'adrenal neoplasms', 'tumour of adrenal gland', 'tumour of the adrenal gland', 'adrenal gland tumour', 'adrenal gland neoplasm (disease)', 'tumor of the adrenal gland', 'adrenal gland tumor', 'neoplasm of the adrenal gland']",,,100091,CN197370,,C2859,0003850,,,,,
mondo:0021228,brainstem neoplasm,"['neoplasm of brainstem', 'tumor of brain stem', 'tumour of brain stem', 'tumour of the brainstem', 'tumor of brainstem', 'brain stem tumor', 'tumour of brainstem', 'tumour of the brain stem', 'Brain stem neoplasm', 'neoplasm of brain stem', 'brain stem tumour', 'neoplasm of the brain stem', 'tumor of the brainstem', 'brainstem tumor', 'brainstem neoplasm (disease)', 'tumor of the brain stem', 'brainstem tumour', 'neoplasm of the brainstem']",,,36414,,,C4869,,,,,,
mondo:0021229,ciliary body neoplasm,"['tumor of the ciliary body', 'tumor of ciliary body', 'ciliary body tumor', 'ciliary body tumour', 'neoplasm of ciliary body', 'tumour of the ciliary body', 'ciliary body neoplasm (disease)', 'neoplasm of the ciliary body', 'tumour of ciliary body']",,,,C0339349,,C4364,,,,,,
mondo:0021230,uterine cervix neoplasm,"['tumor of cervix', 'neoplasm of the uterine cervix', 'cervix', 'neoplasm of uterine cervix', 'tumor of cervix uteri', 'neoplasm of the cervix uteri', 'uterine cervix tumour', 'neoplasm of cervix uteri', 'cervical tumour', 'tumor of uterine cervix', 'tumor of the cervix', 'tumor of the cervix uteri', 'tumour of uterine cervix', 'neoplasm of cervix', 'cervix uteri tumour', 'cervix uteri neoplasm', 'tumour of cervix', 'cervical tumor', 'tumor of the uterine cervix', 'tumour of the cervix', 'neoplasm of the cervix', 'uterine cervix neoplasm (disease)', 'cervix tumor', 'cervix uteri tumor', 'uterine cervix tumor', 'tumour of the uterine cervix', 'tumour of the cervix uteri', 'cervix neoplasm', 'tumour of cervix uteri', 'Cervical neoplasm', 'cervix tumour']",,,,,,C2940,,,,,,
mondo:0021231,retina neoplasm,"['tumor of retina', 'retinal tumor', 'neoplasm of the retina', 'tumor of the retina', 'tumour of the retina', 'retina tumor', 'tumour of retina', 'neoplasm of retina', 'retina neoplasm (disease)', 'retinal tumour', 'retina tumour', 'retinal neoplasm']",,,,,,C4800,1000509,,,,,
mondo:0021232,pineal body neoplasm,"['tumour of the pineal region', 'tumor of pineal area', 'neoplasm of pineal area', 'tumour of pineal region', 'pineal tumor', 'neoplasm of pineal body', 'tumor of the pineal region', 'neoplasm of the pineal area', 'pineal body neoplasm (disease)', 'pineal body tumour', 'pineal region neoplasm', 'tumour of pineal area', 'tumor of the pineal area', 'tumor of pineal body', 'pineal tumour', 'pineal neoplasm', 'pineal area tumor', 'pineal region tumor', 'pineal area neoplasm', 'neoplasm of pineal region', 'pinealoma', 'neoplasm of the pineal region', 'pineal body tumor', 'tumor of pineal region', 'tumour of the pineal area', 'pineal area tumour', 'tumour of pineal body', 'pineal region tumour']",,,,,,C3328,,,,,,
mondo:0021233,ear neoplasm,"['Ear neoplasms', 'ear neoplasm (disease)', 'tumor of the Ear', 'neoplasm of the Ear', 'Ear tumour', 'ear tumor', 'neoplasm of ear', 'tumor of ear', 'tumour of Ear', 'ear tumour', 'tumor of Ear', 'tumour of ear', 'tumour of the Ear', 'neoplasm of Ear', 'Ear tumor']",,,,,,C3000,,,,,,
mondo:0021234,spinal cord neoplasm,"['tumor of spinal cord', 'tumour of the spinal cord', 'tumour of spinal cord', 'neoplasm of spinal cord', 'spinal cord neoplasm (disease)', 'neoplasm of the spinal cord', 'tumor of the spinal cord', 'spinal cord tumour', 'spinal cord tumor']",,,,C0037930,,C3381,,D013120,,,,
mondo:0021235,external ear neoplasm,"['neoplasm of external Ear', 'neoplasm of the external Ear', 'tumour of external Ear', 'tumor of external Ear', 'external Ear tumor', 'external ear tumour', 'external Ear tumour', 'tumor of the external Ear', 'tumor of external ear', 'tumour of external ear', 'neoplasm of external ear', 'tumour of the external Ear', 'external ear neoplasm (disease)', 'external ear tumor']",,,,C0349575,,C4652,,,,,,
mondo:0021237,adrenal medulla neoplasm,"['tumor of adrenal medulla', 'adrenal medulla tumor', 'tumour of adrenal medulla', 'neoplasm of adrenal medulla', 'adrenal medulla neoplasm (disease)', 'adrenal medulla tumour']",,,,C0596046,,C4856,,,,,,
mondo:0021238,cornea neoplasm,"['tumor of cornea', 'corneal tumor', 'corneal tumour', 'tumour of the cornea', 'neoplasm of cornea', 'neoplasm of the cornea', 'tumour of cornea', 'corneal neoplasm', 'tumor of the cornea', 'cornea tumour', 'cornea tumor', 'cornea neoplasm (disease)']",,,,C0339304,,C4361,,,,,,
mondo:0021239,urethra neoplasm,"['tumour of urethra', 'tumour of the urethra', 'urethra neoplasms', 'urethral tumor', 'urethra tumours', 'urethra neoplasm (disease)', 'tumors. urethra', 'urethral tumors', 'urethral neoplasms', 'urethral tumour', 'tumor of urethra', 'urethra tumors', 'neoplasm of the urethra', 'neoplasms. urethra', 'urethra tumour', 'urethral neoplasm', 'urethral tumours', 'tumor of the urethra', 'neoplasm of urethra', 'urethra tumor']",,,,,,C3428,0003846,,,,,
mondo:0021240,tongue neoplasm,"['tumour of the tongue', 'tongue tumour', 'tongue neoplasm (disease)', 'tongue tumor', 'tumor of the tongue', 'neoplasm of tongue', 'neoplasm of the tongue', 'tumour of tongue', 'tumor of tongue']",,,,,,C3416,0003871,,,,,
mondo:0021241,buccal mucosa neoplasm,"['buccal mucosa tumor', 'neoplasm of buccal mucosa', 'neoplasm of the buccal mucosa', 'buccal mucosa tumour', 'tumor of buccal mucosa', 'tumor of the buccal mucosa', 'tumour of the buccal mucosa', 'tumour of buccal mucosa', 'buccal mucosa neoplasm (disease)']",,,,C0345563,,C4405,,,,,,
mondo:0021242,sublingual gland neoplasm,"['tumor of sublingual gland', 'neoplasm of sublingual gland', 'sublingual gland neoplasm (disease)', 'tumour of sublingual gland', 'tumour of the sublingual gland', 'sublingual gland tumor', 'sublingual gland tumour', 'neoplasm of the sublingual gland', 'tumor of the sublingual gland']",,,,C0038554,,C3392,1001430,D013362,,,,
mondo:0021243,parotid gland neoplasm,"['parotid gland tumor', 'parotid tumor', 'tumor of the parotid', 'parotid gland tumour', 'parotid neoplasm', 'tumour of parotid gland', 'tumour of the parotid gland', 'neoplasm of the parotid gland', 'tumor of parotid', 'neoplasm of the parotid', 'parotid tumour', 'parotid gland neoplasm (disease)', 'tumour of parotid', 'tumor of the parotid gland', 'tumour of the parotid', 'neoplasm of parotid', 'neoplasm of parotid gland', 'tumor of parotid gland']",,,,,,C3314,0003873,,,,,
mondo:0021244,submandibular gland neoplasm,"['tumour of the submandibular gland', 'tumor of the submandibular gland', 'neoplasm of submandibular gland', 'tumor of submandibular gland', 'neoplasm of the submandibular gland', 'tumour of submandibular gland', 'submandibular gland tumor', 'submandibular gland neoplasm (disease)', 'submandibular gland tumour']",,,,C0038558,,C3393,1001853,D013365,,,,
mondo:0021245,oral cavity neoplasm,"['mouth tumor', 'mouth tumour', 'oral cavity tumor', 'tumour of oral cavity', 'neoplasm of oral cavity', 'tumor of oral cavity', 'oral cavity neoplasm (disease)', 'tumour of mouth', 'mouth neoplasm', 'oral cavity tumour']",,,,C0026640,,C7606,0003868,,,C00-C14,,
mondo:0021246,pharynx neoplasm,"['neoplasm of the pharynx', 'pharyngeal neoplasms', 'pharyngeal tumor', 'pharynx tumour', 'tumor of the pharynx', 'pharynx neoplasm (disease)', 'tumor of pharynx', 'pharynx tumor', 'tumour of pharynx', 'pharyngeal tumour', 'tumour of the pharynx', 'neoplasm of pharynx']",,,,,,C3325,,,,C00-C14,,
mondo:0021248,nervous system neoplasm,"['nervous system neoplasm (disease)', 'tumor of nervous system', 'nervous system tumour', 'neoplasm of nervous system', 'tumour of the nervous system', 'neoplasm of the nervous system', 'nervous system neoplasms', 'nervous system tumor', 'tumour of nervous system', 'tumor of the nervous system']",,,,,,C3268,,,,,,
mondo:0021249,lip neoplasm,"['tumour of lip', 'lip neoplasm (disease)', 'lip tumor', 'neoplasm of lip', 'tumor of the Lip', 'neoplasm of the Lip', 'tumor of Lip', 'neoplasm of Lip', 'lip neoplasms', 'tumor of lip', 'lip tumour', 'tumour of Lip', 'tumour of the Lip']",,,,,,C3191,,,,C00-C14,,
mondo:0021250,tonsil neoplasm,"['tonsillar neoplasms', 'tonsil tumor', 'tumor of the tonsil', 'tonsillar tumor', 'neoplasm of tonsil', 'tonsil neoplasm (disease)', 'tonsillar neoplasm', 'neoplasm of the tonsil', 'tumour of tonsil', 'tonsillar tumour', 'tumour of the tonsil', 'tonsil tumour', 'tumor of tonsil']",,,,,,C3417,,,,,,
mondo:0021251,endometrium neoplasm,"['tumour of endometrium', 'tumor of endometrium', 'endometrial neoplasm', 'tumor of the endometrium', 'endometrial tumour', 'endometrium tumor', 'endometrium tumour', 'endometrial tumor', 'tumour of the endometrium', 'endometrium neoplasm (disease)', 'neoplasm of endometrium', 'neoplasm of the endometrium']",,,,,,C3012,,D016889,239.5,,,
mondo:0021253,gallbladder neoplasm,"['gall bladder tumor', 'tumor of gall bladder', 'tumour of gallbladder', 'tumor of gallbladder', 'tumor of the gallbladder', 'tumour of gall bladder', 'gallbladder tumour', 'gall bladder tumour', 'neoplasm of the gallbladder', 'gall bladder neoplasm (disease)', 'neoplasm of gall bladder', 'gallbladder tumor', 'tumour of the gallbladder', 'neoplasm of gallbladder']",,,,C0016978,,C3048,,D005706,,,,
mondo:0021254,corpus uteri neoplasm,"['neoplasm of corpus uteri', 'tumor of the uterine corpus', 'neoplasm of the uterine body', 'tumour of uterine corpus', 'tumour of uterine body', 'neoplasm of uterine body', 'uterine body tumour', 'uterine corpus neoplasm', 'neoplasm of the corpus uteri', 'body of uterus tumor', 'uterine body tumor', 'tumor of body of uterus', 'uterine body neoplasm', 'tumor of the uterine body', 'uterine corpus tumour', 'corpus uteri tumor', 'body of uterus neoplasm (disease)', 'tumour of the uterine corpus', 'tumour of the uterine body', 'uterine corpus tumor', 'tumor of corpus uteri', 'neoplasm of the uterine corpus', 'tumour of body of uterus', 'tumor of the corpus uteri', 'neoplasm of the body of uterus', 'tumour of the corpus uteri', 'neoplasm of uterine corpus', 'neoplasm of body of uterus', 'corpus uteri tumour', 'tumour of corpus uteri', 'tumor of uterine body', 'tumor of uterine corpus', 'body of uterus tumour']",,,,C1263777,,C6300,,,,,,
mondo:0021258,choroid neoplasm,"['optic choroid tumor', 'neoplasm of choroid', 'neoplasm of the choroid', 'tumor of optic choroid', 'neoplasm of optic choroid', 'choroidal tumor', 'choroidal neoplasm', 'optic choroid tumour', 'choroid tumour', 'tumour of optic choroid', 'tumour of the choroid', 'choroidal tumour', 'tumour of choroid', 'tumor of choroid', 'optic choroid neoplasm (disease)', 'choroid tumor', 'tumor of the choroid']",,,,,,C2949,,,,,,
mondo:0021259,prostate neoplasm,"['tumour of the prostate', 'prostate tumor', 'prostate gland tumour', 'neoplasm of the prostate', 'tumour of prostate', 'tumor of the prostate', 'tumour of prostate gland', 'prostate gland tumor', 'tumor of prostate', 'neoplasm of prostate', 'neoplasm of prostate gland', 'prostate gland neoplasm (disease)', 'tumor of prostate gland', 'prostate tumour']",13206,,,,,C3343,,,600.1,,,
mondo:0021260,sensory ganglionopathy,"['disease of sensory ganglion', 'sensory ganglion disease or disorder', 'disorder of sensory ganglion']",,,,,,,,,,,,
mondo:0021271,villous adenoma of colon,"['colon villous adenoma', 'colonic villous adenoma', 'villous adenoma of the colon']",,,,C0149862,,C3495,,,,,,
mondo:0021272,inherited orthostatic hypotension,,,,448426,,,,,,,,,
mondo:0021273,leiomyoma of ciliary body,"['ciliary body leiomyoma', 'leiomyoma of the ciliary body']",,,,C0346386,,C4560,,,224.0,,,
mondo:0021275,papilloma of eyelid,"['papilloma of the eyelid', 'eyelid papilloma']",,,,C1142491,,C4061,,,,,,
mondo:0021276,papilloma of buccal mucosa,"['buccal mucosa papilloma', 'papilloma of the buccal mucosa']",,,,C1332641,,C5819,,,210.4,,,
mondo:0021279,mucoepidermoid carcinoma of submandibular gland,"['mucoepidermoid carcinoma of the submandibular gland', 'submandibular gland mucoepidermoid carcinoma']",,,,C1336524,,C5939,,,,,,
mondo:0021280,mucoepidermoid carcinoma of parotid gland,"['mucoepidermoid carcinoma of the parotid', 'parotid gland mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of parotid', 'parotid mucoepidermoid carcinoma', 'mucoepidermoid carcinoma of the parotid gland']",,,,C1335363,,C5938,,,,,,
mondo:0021281,cavernous hemangioma of retina,"['cavernous hemangioma of the retina', 'retinal cavernous angioma', 'cavernous angioma of retina', 'retina cavernous hemangioma', 'retinal cavernous hemangioma', 'retina cavernous angioma', 'cavernous angioma of the retina']",,,,C0730304,,C4921,,,,,,
mondo:0021282,malignant teratoma of testis,"['malignant teratoma of the testis', 'testis malignant teratoma', 'testicular immature teratoma', 'testicular malignant teratoma', 'immature testicular teratoma', 'malignant testicular teratoma', 'immature teratoma of the testis', 'immature teratoma of testis']",,,,C1334154,,C6353,,,186.9,,,
mondo:0021283,malignant teratoma of mediastinum,"['immature malignant teratoma of mediastinum', 'malignant mediastinal teratoma', 'immature malignant teratoma of the mediastinum', 'mediastinal immature malignant teratoma', 'malignant teratoma of the mediastinum', 'mediastinum malignant teratoma']",,,,C0349663,,C4668,,,,,,
mondo:0021284,carcinoma in situ of ureter,"['carcinoma in situ of ureter', 'ureteral carcinoma in situ', 'ureter in situ carcinoma', 'ureter cancer stage 0is', 'carcinoma in situ of the ureter', 'ureter carcinoma in situ', 'stage 0 ureter carcinoma', 'stage 0is carcinoma of ureter', 'stage 0is ureter cancer aJCC v7', 'stage 0is ureter carcinoma', 'stage 0is ureter urothelial cancer', 'stage 0is carcinoma of the ureter', 'stage 0is ureter urothelial carcinoma', 'stage 0is ureter urothelial carcinoma aJCC v7', 'stage 0is ureteral carcinoma', 'stage 0is ureter cancer']",,,,C0346267,,C4529,,,233.9,,,
mondo:0021285,carcinoma in situ of urethra,"['stage 0is carcinoma of urethra', 'stage 0is urethral cancer aJCC v7', 'urethra in situ carcinoma', 'urethral carcinoma in situ', 'stage 0is carcinoma of the urethra', 'stage 0 urethra carcinoma', 'stage 0is urethral carcinoma', 'urethra carcinoma in situ', 'stage 0is urethra carcinoma', 'stage 0is urethral cancer', 'carcinoma in situ of urethra', 'carcinoma in situ of the urethra']",,,,C0346280,,C4531,,,233.9,,,
mondo:0021287,carcinoma in situ of epiglottis,"['stage 0 epiglottic carcinoma aJCC v7', 'stage 0 epiglottic carcinoma aJCC v8', 'carcinoma in situ of epiglottis', 'Epiglottis carcinoma in situ', 'carcinoma in situ of the Epiglottis', 'stage 0 epiglottic carcinoma', 'stage 0 epiglottic carcinoma aJCC v6', 'stage 0 epiglottic carcinoma aJCC v6, v7, and v8', 'stage 0 epiglottic throat cancer', 'stage 0 epiglottis carcinoma', 'epiglottis in situ carcinoma', 'epiglottic carcinoma in situ']",,,,C0347103,,C4592,,,,,,
mondo:0021288,carcinoma in situ of hypopharynx,"['stage 0 hypopharyngeal carcinoma in situ', 'stage 0 hypopharyngeal carcinoma aJCC v8', 'stage 0 hypopharyngeal carcinoma', 'stage 0 hypopharynx carcinoma', 'carcinoma in situ of the hypopharynx', 'stage 0 hypopharyngeal throat cancer', 'stage 0 hypopharyngeal carcinoma aJCC v7', 'carcinoma in situ of hypopharynx', 'stage 0 carcinoma of hypopharynx', 'hypopharynx carcinoma in situ', 'hypopharyngeal carcinoma in situ', 'hypopharynx in situ carcinoma', 'stage 0 hypopharyngeal cancer', 'stage 0 hypopharyngeal carcinoma aJCC v6', 'stage 0 hypopharyngeal carcinoma aJCC v6, v7, and v8', 'stage 0 carcinoma of the hypopharynx']",,,,C4331310,,C9101,,,,,,
mondo:0021289,carcinoma in situ of cecum,"['stage 0 caecum carcinoma', 'cecum carcinoma in situ aJCC v6', 'carcinoma in situ of the cecum', 'caecum in situ carcinoma', 'carcinoma in situ of caecum', 'cecum carcinoma in situ', 'stage 0 cecum carcinoma', 'cecum carcinoma in situ aJCC v7']",,,,C0347126,,C4594,,,,,,
mondo:0021290,carcinoma in situ of appendix,"['stage 0 vermiform appendix carcinoma', 'carcinoma in situ of the appendix', 'stage 0 appendix cancer', 'stage 0 appendix carcinoma', 'carcinoma in situ of vermiform appendix', 'stage 0 appendix carcinoma aJCC v7', 'vermiform appendix in situ carcinoma']",,,,C0347125,,C4593,,,,,,
mondo:0021291,carcinoma in situ of fundus of stomach,"['fundus of stomach in situ carcinoma', 'carcinoma in situ of gastric fundus', 'gastric fundus carcinoma in situ', 'stage 0 fundus of stomach carcinoma', 'stage 0 gastric fundus carcinoma', 'carcinoma in situ of the gastric fundus', 'carcinoma in situ of fundus of stomach', 'gastric fundus carcinoma in situ aJCC v6 and v7', 'carcinoma in situ of the fundus of the stomach']",,,,C0345800,,C4429,,,,,,
mondo:0021292,carcinoma in situ of gastric body,"['gastric body carcinoma in situ aJCC v6 and v7', 'stage 0 gastric body carcinoma', 'stage 0 body of stomach carcinoma', 'carcinoma in situ of the body of the stomach', 'gastric body carcinoma in situ', 'body of stomach in situ carcinoma', 'carcinoma in situ of the gastric body', 'carcinoma in situ of body of stomach']",,,,C0345805,,C4430,,,,,,
mondo:0021294,carcinoma in situ of gastric cardia,"['carcinoma in situ of cardia of stomach', 'stage 0 cardia of stomach carcinoma', 'carcinoma in situ of the gastric cardia', 'gastric cardia carcinoma in situ', 'gastric cardia carcinoma in situ aJCC v6 and v7', 'stage 0 gastric cardia carcinoma', 'carcinoma in situ of the cardia of the stomach', 'cardia of stomach in situ carcinoma']",,,,C0345795,,C4428,,,,,,
mondo:0021296,carcinoma in situ of renal pelvis,"['carcinoma in situ of kidney pelvis', 'renal pelvis carcinoma in situ', 'stage 0is kidney pelvis carcinoma', 'stage 0is renal pelvis cancer', 'stage 0is carcinoma of the kidney pelvis', 'carcinoma in situ of the kidney pelvis', 'carcinoma in situ of the renal pelvis', 'kidney pelvis carcinoma in situ', 'stage 0is renal pelvis urothelial carcinoma', 'stage 0is carcinoma of kidney pelvis', 'stage 0is carcinoma of renal pelvis', 'stage 0is kidney renal pelvis urothelial cancer', 'stage 0is renal pelvis urothelial carcinoma aJCC v7', 'carcinoma in situ of renal pelvis', 'stage 0 renal pelvis carcinoma', 'renal pelvis in situ carcinoma', 'stage 0is renal pelvis cancer aJCC v7', 'stage 0is carcinoma of the renal pelvis']",,,,C0347184,,C4597,,,233.9,,,
mondo:0021297,carcinoma in situ of nasopharynx,"['stage 0 carcinoma of the nasopharynx', 'nasopharynx in situ carcinoma', 'stage 0 nasopharynx carcinoma', 'carcinoma in situ of the nasopharynx', 'stage 0 nasopharyngeal carcinoma in situ', 'stage 0 nasopharyngeal carcinoma aJCC v6, v7, and v8', 'stage 0 nasopharyngeal carcinoma aJCC v8', 'stage 0 nasopharyngeal cancer', 'stage 0 nasopharyngeal carcinoma aJCC v6', 'stage 0 nasopharyngeal carcinoma aJCC v7', 'stage 0 carcinoma of nasopharynx', 'stage 0 nasopharyngeal throat cancer', 'nasopharyngeal carcinoma in situ', 'carcinoma in situ of nasopharynx', 'stage 0 nasopharyngeal carcinoma']",,,,C4331312,,C9099,,,,,,
mondo:0021298,carcinoma in situ of oropharynx,"['oropharynx carcinoma in situ', 'stage 0 oropharyngeal carcinoma', 'stage 0 oropharyngeal carcinoma in situ', 'stage 0 oropharyngeal carcinoma aJCC v7', 'stage 0 oropharynx carcinoma', 'stage 0 carcinoma of oropharynx', 'oropharyngeal carcinoma in situ', 'stage 0 carcinoma of the oropharynx', 'oropharyngeal cancer stage 0', 'stage 0 oropharyngeal cancer', 'oropharynx in situ carcinoma', 'stage 0 oropharyngeal carcinoma aJCC v6', 'carcinoma in situ of the oropharynx', 'stage 0 oropharyngeal carcinoma aJCC v6 and v7', 'carcinoma in situ of oropharynx', 'stage 0 oropharyngeal throat cancer']",,,,C0347099,,C4590,,,,,,
mondo:0021299,carcinoma in situ of extrahepatic bile duct,"['stage 0 carcinoma of the extrahepatic bile duct', 'stage 0 carcinoma of extrahepatic bile duct', 'carcinoma in situ of the extrahepatic bile duct', 'extrahepatic bile duct carcinoma in situ', 'stage 0 extrahepatic bile duct carcinoma', 'extrahepatic bile duct cancer stage 0', 'stage 0 extrahepatic bile duct cancer', 'carcinoma in situ of extrahepatic bile duct', 'carcinoma in situ of extrahepatic biliary ducts', 'extrahepatic bile duct in situ carcinoma', 'carcinoma in situ of extrahepatic bile ducts', 'extrahepatic biliary duct carcinoma in situ', 'stage 0 extrahepatic bile duct carcinoma in situ']",,,,C0345914,,C4442,,,,,,
mondo:0021300,adenoid cystic carcinoma of oropharynx,"['oropharyngeal adenoid cystic carcinoma', 'oropharynx adenoid cystic carcinoma', 'adenoid cystic carcinoma of the oropharynx', 'oropharyngeal throat adenoid cystic cancer']",,,,C1335139,,C6241,,,,,,
mondo:0021301,adenoma of nipple,"['papillomatosis, subareolar duct', 'subareolar duct papillomatosis', 'nipple adenoma', 'adenoma of the nipple']",,,,C0334378,,C4192,,,,,,
mondo:0021303,adenoma of small intestine,"['adenoma of the small bowel', 'adenoma of small bowel', 'adenoma of the small intestine', 'small intestinal adenoma', 'small bowel adenoma', 'small intestine adenoma']",,,,C1302392,,C5340,,,,,,
mondo:0021309,malignant neoplasm of endocervix,"['malignant tumour of the endocervix', 'malignant endocervical neoplasm', 'malignant endocervix neoplasm', 'malignant tumour of the uterine endocervix', 'malignant tumour of uterine endocervix', 'malignant neoplasm of uterine endocervix', 'malignant uterine endocervix tumour', 'malignant neoplasm of the endocervix', 'cancer of endocervix', 'malignant endocervix tumor', 'malignant tumor of the uterine endocervix', 'malignant uterine endocervix tumor', 'malignant endocervical tumour', 'malignant endocervix tumour', 'malignant uterine endocervix neoplasm', 'malignant neoplasm of the uterine endocervix', 'malignant tumor of endocervix', 'malignant neoplasm of endocervix', 'malignant tumour of endocervix', 'malignant tumor of the endocervix', 'endocervix cancer', 'malignant endocervical tumor', 'malignant tumor of uterine endocervix']",,,,,,C3553,,,180.0,C53.0,,
mondo:0021310,malignant tumor of neck,"['cancer of neck', 'neck cancer', 'malignant neck neoplasm', 'malignant neoplasm of neck', 'malignant tumour of the neck', 'malignant tumor of the neck', 'cancer of the neck', 'malignant neck tumour', 'malignant neoplasm of the neck', 'malignant neck tumor']",,,,C0746787,,C4940,,,,,,
mondo:0021311,malignant tumor of parathyroid gland,"['malignant tumour of the parathyroid', 'malignant parathyroid neoplasm', 'parathyroid cancer', 'malignant neoplasm of the parathyroid gland', 'malignant tumor of the parathyroid', 'malignant parathyroid gland neoplasm', 'malignant parathyroid tumor', 'malignant tumour of parathyroid', 'malignant neoplasm of the parathyroid', 'malignant parathyroid gland tumour', 'malignant parathyroid tumour', 'malignant tumor of the parathyroid gland', 'malignant tumor of parathyroid', 'malignant neoplasm of parathyroid', 'malignant tumour of the parathyroid gland', 'malignant parathyroid gland tumor', 'cancer of parathyroid gland', 'malignant neoplasm of parathyroid gland', 'parathyroid gland cancer']",,,,,,C9322,,,194.1,,,
mondo:0021312,malignant tumor of adrenal cortex,"['malignant neoplasm of adrenal cortex', 'malignant adrenocortical neoplasm', 'malignant adrenal cortex tumor', 'malignant adrenocortical tumour', 'malignant tumor of the adrenal cortex', 'malignant neoplasm of the adrenal cortex', 'malignant adrenocortical tumor', 'malignant tumour of the adrenal cortex', 'malignant adrenal cortex neoplasm', 'malignant adrenal cortex tumour', 'adrenal cortex cancer', 'cancer of adrenal cortex']",,,,,,C9327,,,,,,
mondo:0021313,eyelid cancer,"['malignant tumor of eyelid', 'malignant tumour of eyelid', 'malignant tumour of the eyelid', 'malignant eyelid neoplasm', 'eyelid cancer', 'malignant eyelid tumour', 'malignant eyelid tumor', 'malignant neoplasm of the eyelid', 'cancer of eyelid', 'malignant tumor of the eyelid', 'malignant neoplasm of eyelid']",,,,,,C6786,,,173.1,,,
mondo:0021315,malignant tumor of nasopharynx,"['cancer of nasopharynx', 'malignant nasopharyngeal tumor', 'malignant tumour of the nasopharynx', 'malignant tumor of the nasopharynx', 'malignant nasopharynx neoplasm', 'malignant neoplasm of the nasopharynx', 'malignant neoplasm of nasopharynx', 'nasopharynx cancer', 'malignant nasopharyngeal tumour', 'malignant nasopharyngeal neoplasm']",,,,C0238301,,C9321,,,147.9,,,
mondo:0021316,malignant tumor of minor salivary gland,"['malignant minor salivary gland tumour', 'malignant tumor of the minor salivary gland', 'malignant minor salivary gland tumor', 'malignant tumour of the minor salivary gland', 'cancer of minor salivary gland', 'malignant minor salivary gland neoplasm', 'malignant neoplasm of minor salivary gland', 'minor salivary gland cancer', 'malignant neoplasm of the minor salivary gland']",,,,C0345614,,C4410,,,,,,
mondo:0021317,cancer of cerebellum,"['malignant tumor of the cerebellum', 'malignant tumour of cerebellum', 'malignant tumor of cerebellum', 'cerebellar tumor, malignant', 'malignant cerebellar neoplasm', 'cancer of cerebellum', 'cerebellar neoplasm, malignant', 'malignant cerebellar tumor', 'malignant tumour of the cerebellum', 'malignant cerebellar tumour', 'malignant neoplasm of cerebellum', 'malignant cerebellum neoplasm', 'malignant neoplasm of the cerebellum', 'malignant cerebellar neoplasms', 'cerebellum cancer', 'cancer of the cerebellum', 'cerebellar cancer']",,,,,,C3569,,,191.6,,,
mondo:0021320,malignant tumor of floor of mouth,"['malignant neoplasm of mouth floor', 'malignant floor of the mouth tumour', 'malignant floor of the mouth neoplasm', 'cancer of mouth floor', 'malignant floor of mouth tumour', 'malignant floor of the mouth tumor', 'malignant floor of mouth neoplasm', 'malignant tumor of the floor of the mouth', 'mouth floor cancer', 'malignant tumour of the floor of the mouth', 'malignant neoplasm of floor of mouth', 'malignant neoplasm of the floor of the mouth', 'malignant floor of mouth tumor', 'malignant mouth floor neoplasm']",,,,,,C9318,,,144.9,,,
mondo:0021321,malignant tumor of extrahepatic bile duct,"['cancer of extrahepatic bile duct', 'malignant tumor of the extrahepatic bile duct', 'malignant neoplasm of extrahepatic bile duct', 'malignant extrahepatic bile duct tumour', 'malignant neoplasm of the extrahepatic bile duct', 'malignant tumour of the extrahepatic bile duct', 'malignant extrahepatic bile duct tumor', 'extrahepatic bile duct cancer', 'malignant extrahepatic bile duct neoplasm']",,,,C0153453,,C7483,,,156.8,,,
mondo:0021322,malignant tumor of meninges,"['malignant meninges neoplasm', 'meningeal cluster cancer', 'malignant meninges tumour', 'malignant neoplasm of the meninges', 'meningeal tumors, malignant', 'meningeal cancer', 'malignant neoplasm of meningeal cluster', 'malignant tumour of the meninges', 'cancer of meningeal cluster', 'malignant meninges tumor', 'malignant tumor of the meninges', 'cancer of meninges', 'malignant meningeal tumor', 'malignant neoplasms of meninges', 'malignant neoplasm of meninges', 'cancer of the meninges', 'malignant meningeal tumour', 'malignant meningeal neoplasms', 'malignant meningeal cluster neoplasm']",,,,C0348375,,C4628,,,,,,
mondo:0021323,malignant neoplasm of chest wall,"['malignant tumor of the chest wall', 'malignant neoplasm of chest wall', 'chest wall cancer', 'cancer of chest wall', 'malignant neoplasm of the chest wall', 'malignant tumour of chest wall', 'malignant chest wall tumor', 'malignant tumour of the chest wall', 'malignant tumor of chest wall', 'malignant chest wall neoplasm', 'malignant chest wall tumour']",,,,C0346948,,C4580,,,,,,
mondo:0021324,malignant neoplasm of abdominal esophagus,"['malignant neoplasm of abdominal part of oesophagus', 'abdominal part of oesophagus cancer', 'cancer of abdominal part of esophagus', 'malignant abdominal part of oesophagus neoplasm', 'malignant neoplasm of the abdominal oesophagus', 'abdominal part of esophagus cancer', 'malignant tumour of the abdominal oesophagus', 'malignant tumor of the abdominal esophagus', 'cancer of abdominal part of oesophagus', 'malignant abdominal part of esophagus neoplasm', 'malignant neoplasm of the abdominal esophagus', 'malignant neoplasm of abdominal part of esophagus']",,,,C0496775,,C4764,,,150.2,,,
mondo:0021325,malignant neoplasm of thoracic esophagus,"['malignant thoracic part of oesophagus neoplasm', 'malignant neoplasm of thoracic part of oesophagus', 'thoracic part of esophagus cancer', 'malignant thoracic part of esophagus neoplasm', 'thoracic part of oesophagus cancer', 'malignant neoplasm of thoracic part of esophagus', 'malignant neoplasm of the thoracic esophagus', 'malignant neoplasm of the thoracic oesophagus', 'cancer of thoracic part of esophagus', 'cancer of thoracic part of oesophagus']",,,,C0153411,,C3532,,,150.1,,,
mondo:0021326,malignant neoplasm of cervical esophagus,"['cervical part of oesophagus cancer', 'cancer of cervical part of esophagus', 'malignant neoplasm of cervical part of oesophagus', 'cervical part of esophagus cancer', 'malignant neoplasm of the cervical oesophagus', 'malignant neoplasm of cervical part of esophagus', 'malignant cervical part of oesophagus neoplasm', 'malignant cervical part of esophagus neoplasm', 'malignant neoplasm of the cervical esophagus', 'cancer of cervical part of oesophagus']",,,,C0496773,,C4763,,,150.0,,,
mondo:0021327,carcinoma of urethra,"['carcinoma of urethra', 'urethral carcinoma', 'urethral cancer', 'urethra carcinoma', 'carcinoma of the urethra']",,,,,,C9106,,,,,,
mondo:0021329,carcinoma of soft palate,"['soft palate cancer', 'carcinoma of soft palate', 'carcinoma of the soft palate', 'soft palate carcinoma']",,,,C0345555,,C8395,,,,,,
mondo:0021331,carcinoma of parotid gland,"['carcinoma of the parotid gland', 'carcinoma of parotid gland', 'parotid gland cancer', 'parotid gland carcinoma', 'parotid carcinoma', 'carcinoma of the parotid', 'carcinoma of parotid']",,,,C0345602,,C6791,1000460,,,,,
mondo:0021333,carcinoma of lip,"['lip carcinoma', 'lip cancer', 'carcinoma of the Lip', 'carcinoma of lip']",,,,C0149637,,C3490,,,,,,
mondo:0021334,immunoproliferative disorder,"['Immunoproliferative disorder', 'Immunoproliferative Disorder', 'Immunoproliferative Disorders', 'Disorder, Immunoproliferative', 'Disorders, Immunoproliferative', 'Immunoproliferative disease']",,,,C0021070,,,,D007160,203.80,,,
mondo:0021335,carcinoma of duodenum,"['duodenal carcinoma', 'cancer of duodenum', 'carcinoma of the duodenum', 'carcinoma of duodenum', 'cancer of the duodenum', 'duodenum carcinoma', 'duodenal cancer']",,,,,,C4803,,,,,,
mondo:0021337,tonsil carcinoma,"['tonsil cancer', 'carcinoma of the tonsil', 'carcinoma of tonsil', 'tonsillar carcinoma', 'tonsil carcinoma', 'cancer of the tonsil', 'tonsillar cancer', 'cancer of tonsil']",,,,C0558355,,C4825,,,,,,
mondo:0021339,carcinoma of hard palate,"['carcinoma of hard palate', 'hard palate carcinoma', 'carcinoma of the hard palate']",,,,C0345550,,C8394,,,,,,
mondo:0021340,intertrigo,"['Intertrigo', 'Eczema intertrigo', 'Erythema intertrigo']",,,,C0021807,,,,D007402,695.89,,,
mondo:0021343,carcinoma of floor of mouth,"['floor of the mouth carcinoma', 'mouth floor carcinoma', 'carcinoma of mouth floor', 'carcinoma of the floor of the mouth', 'mouth floor cancer', 'floor of mouth carcinoma']",,,,,,C9319,,,,,,
mondo:0021345,carcinoma of pharynx,"['cancer of the pharynx', 'carcinoma of the pharynx', 'pharyngeal carcinoma', 'pharyngeal throat cancer', 'carcinoma of pharynx', 'pharynx carcinoma']",,,,,,C9466,,,,,,
mondo:0021348,neoplasm of testis,"['testicular tumour', 'testicular tumor', 'tumor of testis', 'neoplasm of the testis', 'testis tumour', 'tumour of the testis', 'neoplasm of testis', 'testis neoplasm', 'testis tumor', 'tumour of testis', 'testis neoplasm (disease)', 'tumor of the testis', 'testicular neoplasm']",,,,,,C3404,0004281,,239.5,,,
mondo:0021350,neoplasm of thorax,"['tumor of the thorax', 'neoplasm of thoracic segment of trunk', 'thoracic segment of trunk neoplasm (disease)', 'thoracic segment of trunk tumor', 'thoracic tumour', 'tumor of thoracic segment of trunk', 'thoracic neoplasm', 'tumour of the thorax', 'thoracic segment of trunk tumour', 'tumour of thoracic segment of trunk', 'thoracic tumor', 'neoplasm of the thorax', 'tumour of thorax', 'tumor of thorax']",,,,C0039981,,C3406,,,239.89,C30-C39,,
mondo:0021351,neoplasm of neck,"['tumour of neck', 'tumor of the neck', 'tumour of the neck', 'neoplasm of the neck', 'neck neoplasm', 'neck tumor', 'tumor of neck', 'neck neoplasms (Including All pharyngeal related neoplasms)', 'neoplasm of neck', 'neck neoplasm (disease)', 'neck tumour']",,,,C0027533,,C3260,,,239.89,,,
mondo:0021353,tumor of uterus,"['uterus neoplasm (disease)', 'uterine tumour', 'tumour of the uterus', 'uterine neoplasms', 'uterus neoplasm', 'uterine neoplasm', 'neoplasm of the uterus', 'uterus tumour', 'uterine tumor', 'neoplasm of uterus', 'uterus tumor', 'tumor of the uterus', 'tumor of uterus']",,,,,,C3435,0003859,,239.5,,,
mondo:0021354,tumor of adipose tissue,"['adipose tissue tumour', 'lipomatous tumor', 'neoplasm of the adipose tissue', 'tumor of the adipose tissue', 'lipomatous tumour', 'adipose tissue neoplasm', 'adipose tissue tumor', 'neoplasm of adipose tissue', 'lipomatous neoplasm', 'tumor of adipose tissue', 'tumour of the adipose tissue', 'adipose tissue neoplasm (disease)']",,,,C0206631,,C4248,,,239.2,,,
mondo:0021355,neoplasm of esophagus,"['tumour of the oesophagus', 'tumour of oesophagus', 'tumor of esophagus', 'esophageal tumor', 'esophageal tumors', 'esophageal neoplasms, benign and malignant', 'tumor of the esophagus', 'oesophagus neoplasm', 'neoplasm of the esophagus', 'oesophagus tumour', 'oesophagus neoplasm (disease)', 'neoplasm of the oesophagus', 'esophageal neoplasm', 'esophageal tumours', 'esophagus tumor', 'neoplasm of esophagus', 'esophagus neoplasm (disease)', 'esophageal tumour', 'esophagus neoplasm']",,,,C0014859,,C3028,,,,,,
mondo:0021357,tumor of salivary gland,"['tumour of the salivary gland', 'saliva-secreting gland tumor', 'neoplasm of saliva-secreting gland', 'salivary gland tumor', 'saliva-secreting gland tumour', 'salivary gland tumour', 'tumour of saliva-secreting gland', 'salivary gland neoplasm', 'neoplasm of the salivary gland', 'neoplasm of salivary gland', 'saliva-secreting gland neoplasm (disease)', 'tumor of saliva-secreting gland', 'tumor of the salivary gland']",,,,,,C3361,0003826,,,,,
mondo:0021358,neoplasm of hypopharynx,"['hypopharyngeal tumour', 'hypopharynx tumour', 'hypopharyngeal neoplasms', 'neoplasm of hypopharynx', 'neoplasm of the hypopharynx', 'hypopharyngeal tumor', 'tumor of hypopharynx', 'hypopharynx tumor', 'hypopharyngeal neoplasm', 'tumour of the hypopharynx', 'tumor of the hypopharynx', 'tumour of hypopharynx', 'hypopharynx neoplasm (disease)']",,,,,,C3127,,,,,,
mondo:0021360,tumor of parathyroid gland,"['tumor of parathyroid', 'parathyroid gland neoplasm (disease)', 'parathyroid gland neoplasm', 'tumor of parathyroid gland', 'tumor of the parathyroid gland', 'neoplasm of parathyroid gland', 'parathyroid gland tumor', 'neoplasm of the parathyroid', 'neoplasm of the parathyroid gland', 'parathyroid tumour', 'parathyroid neoplasm', 'tumor of the parathyroid', 'tumour of parathyroid', 'tumour of the parathyroid', 'tumour of the parathyroid gland', 'parathyroid tumor', 'neoplasm of parathyroid', 'parathyroid gland tumour']",,,,,,C3313,,,239.7,,,
mondo:0021364,neoplasm of oropharynx,"['oropharynx tumor', 'oropharyngeal neoplasms', 'oropharyngeal neoplasm', 'neoplasm of the oropharynx', 'tumor of the oropharynx', 'tumor of oropharynx', 'oropharynx neoplasm (disease)', 'tumour of oropharynx', 'tumour of the oropharynx', 'oropharynx tumour', 'oropharyngeal tumor', 'oropharyngeal tumour', 'neoplasm of oropharynx']",,,,C0029295,,C3291,,,,,,
mondo:0021366,neoplasm of middle ear,"['tumor of the middle Ear', 'middle ear tumour', 'middle Ear tumour', 'middle Ear neoplasm', 'middle ear tumor', 'neoplasm of middle ear', 'tumor of middle Ear', 'middle ear neoplasm (disease)', 'middle Ear tumor', 'tumour of middle ear', 'tumour of the middle Ear', 'tumour of middle Ear', 'tumor of middle ear', 'neoplasm of the middle Ear']",,,,,,C4412,,,239.89,,,
mondo:0021367,"leukemia, myeloid, accelerated-phase","['Aggressive-Phase Chronic Myelocytic Leukaemia', 'Accelerated Phase CML', 'Aggressive-Phase Chronic Myeloid Leukaemia', 'Myeloid Leukemia, Chronic, Accelerated Phase', 'Aggressive-Phase Chronic Myelogenous Leukaemia', 'Accelerated Phase Chronic Myelogenous Leukaemia', 'Accelerated Phase Chronic Myelocytic Leukaemia', 'CML ACCELERATED', 'Accelerated phase chronic myeloid leukaemia', 'Myeloid Leukemia, Chronic, Aggressive Phase', 'Aggressive-Phase CML', 'Myelogenous Leukemia, Chronic, Aggressive-Phase', 'Accelerated Phase Chronic Myeloid Leukaemia', 'Myeloid Leukemia, Chronic, Aggressive-Phase', 'Accelerated Phase Chronic Myelogenous Leukemia, BCR-ABL1 Positive', 'Accelerated Phase Chronic Myelocytic Leukemia', 'Aggressive-Phase Chronic Myeloid Leukemia', 'Leukemia, Myeloid, Aggressive-Phase', 'Accelerated Phase Chronic Granulocytic Leukaemia', 'Aggressive-Phase Chronic Myelogenous Leukemia', 'Accelerated phase chronic myeloid leukemia', 'Accelerated Phase Chronic Myeloid Leukemia', 'Myeloid Leukemia, Chronic, Accelerated-Phase', 'Accelerated Phase Chronic Granulocytic Leukemia', 'Leukemia, Myeloid, Accelerated Phase', 'Leukemia, Myeloid, Accelerated-Phase', 'CML AGGRESSIVE', 'Myelogenous Leukemia, Chronic, Aggressive Phase', 'Leukemia, Myelogenous, Aggressive-Phase', 'Leukemia, Myelogenous, Aggressive Phase', 'Accelerated Phase Chronic Myelogenous Leukemia', 'Aggressive-Phase Chronic Myelocytic Leukemia']",,,,C0023472,,,1001755,D015465,,,,
mondo:0021368,neoplasm of major salivary gland,"['tumour of Major salivary gland', 'neoplasm of major salivary gland', 'tumour of the Major salivary gland', 'major salivary gland tumor', 'tumour of major salivary gland', 'tumor of the Major salivary gland', 'tumor of major salivary gland', 'neoplasm of the Major salivary gland', 'major salivary gland tumour', 'major salivary gland neoplasm', 'major salivary gland neoplasm (disease)', 'tumor of Major salivary gland']",,,,C0345599,,C4407,,,,,,
mondo:0021370,neoplasm of minor salivary gland,"['minor salivary gland neoplasm', 'neoplasm of the minor salivary gland', 'minor salivary gland tumour', 'tumor of the minor salivary gland', 'tumour of minor salivary gland', 'tumour of the minor salivary gland', 'minor salivary gland neoplasm (disease)', 'minor salivary gland tumor', 'neoplasm of minor salivary gland', 'tumor of minor salivary gland']",,,,C0345613,,C4409,,,,,,
mondo:0021372,neoplasm of temporal lobe,"['tumour of temporal lobe', 'neoplasm of temporal lobe', 'temporal lobe tumor', 'temporal lobe neoplasm', 'tumor of the temporal lobe', 'tumour of the temporal lobe', 'neoplasm of the temporal lobe', 'temporal lobe neoplasm (disease)', 'tumor of temporal lobe', 'temporal lobe tumour']",,,,C1263887,,C5567,,,,,,
mondo:0021373,neoplasm of parietal lobe,"['tumor of parietal lobe', 'neoplasm of the parietal lobe', 'neoplasm of parietal lobe', 'parietal lobe tumor', 'tumour of the parietal lobe', 'parietal lobe tumour', 'tumour of parietal lobe', 'tumor of the parietal lobe', 'parietal lobe neoplasm (disease)']",,,,C1263888,,C5573,,,,,,
mondo:0021374,neoplasm of cerebral hemisphere,"['cerebral tumor', 'tumour of cerebral hemisphere', 'tumor of the cerebral hemispheres', 'telencephalon tumor', 'cerebral neoplasm', 'neoplasm of the cerebral hemispheres', 'tumour of cerebral hemispheres', 'tumor of cerebrum', 'neoplasm of cerebral hemisphere', 'cerebral hemispheric tumor', 'cerebral tumour', 'neoplasm of cerebrum', 'cerebral neoplasms', 'tumor of the cerebrum', 'tumour of the cerebrum', 'cerebral hemisphere tumor', 'cerebral hemisphere tumour', 'tumor of cerebral hemisphere', 'telencephalon neoplasm (disease)', 'neoplasm of cerebral hemispheres', 'cerebral hemispheric tumour', 'tumour of cerebrum', 'tumour of the cerebral hemispheres', 'tumor of cerebral hemispheres', 'tumour of telencephalon', 'neoplasm of telencephalon', 'neoplasm of the cerebrum', 'cerebral hemispheric neoplasm', 'tumor of telencephalon', 'telencephalon tumour']",,,,,,C4874,,,,,,
mondo:0021375,tumor of duodenum,"['duodenal tumor', 'tumor of duodenum', 'duodenal neoplasm', 'neoplasm of duodenum', 'neoplasm of the duodenum', 'duodenum neoplasm (disease)', 'duodenum tumour', 'tumor of the duodenum', 'duodenal tumour', 'tumour of the duodenum', 'duodenum tumor']",,,,,,C2995,,,,,,
mondo:0021377,hypertrophic lichen planus,"['Hypertrophic lichen planus', 'hypertrophic lichen planus', 'Lichen planus hypertrophicus', 'Hypertrophic Lichen Planus']",,,,C0023649,,C34779,,,,,,
mondo:0021378,neoplasm of endocardium,"['endocardial neoplasm', 'endocardial tumour', 'endocardium tumor', 'tumour of the endocardium', 'endocardium tumour', 'tumor of endocardium', 'tumor of the endocardium', 'neoplasm of the endocardium', 'tumour of endocardium', 'endocardium neoplasm (disease)', 'neoplasm of endocardium', 'endocardial tumor']",,,,C1290401,,C5346,,,239.89,,,
mondo:0021379,neoplasm of epicardium,"['epicardial tumour', 'epicardium neoplasm (disease)', 'tumour of the epicardium', 'epicardium tumour', 'epicardial neoplasm', 'tumor of epicardium', 'epicardium tumor', 'neoplasm of epicardium', 'tumour of epicardium', 'epicardial tumor', 'neoplasm of the epicardium', 'tumor of the epicardium']",,,,C1290403,,C5347,,,239.89,,,
mondo:0021380,neoplasm of myocardium,"['myocardium tumor', 'tumour of myocardium', 'neoplasm of myocardium', 'myocardial tumour', 'neoplasm of the myocardium', 'tumor of myocardium', 'myocardium tumour', 'myocardium neoplasm (disease)', 'myocardial neoplasm', 'tumour of the myocardium', 'tumor of the myocardium', 'myocardial tumor']",,,,C1290402,,C5349,,,239.89,,,
mondo:0021381,neoplasm of pericardium,"['pericardium tumour', 'pericardial tumour', 'pericardial tumor', 'pericardium tumor', 'pericardial neoplasm', 'tumor of the pericardium', 'tumour of pericardium', 'pericardium neoplasm (disease)', 'neoplasm of the pericardium', 'neoplasm of pericardium', 'tumor of pericardium', 'tumour of the pericardium']",,,,,,C4651,,,239.89,,,
mondo:0021383,neoplasm of floor of mouth,"['neoplasm of mouth floor', 'floor of the mouth tumor', 'tumor of floor of mouth', 'floor of the mouth neoplasm', 'floor of mouth tumour', 'mouth floor tumor', 'mouth floor neoplasm (disease)', 'neoplasm of the floor of the mouth', 'tumor of mouth floor', 'tumour of floor of mouth', 'tumour of the floor of the mouth', 'tumor of the floor of the mouth', 'tumour of mouth floor', 'floor of the mouth tumour', 'floor of mouth neoplasm', 'floor of mouth tumor', 'mouth floor tumour']",,,,C0345538,,C4401,,,,,,
mondo:0021385,extrahepatic bile duct neoplasm,"['extrahepatic bile duct neoplasm', 'tumour of the extrahepatic bile duct', 'neoplasm of the extrahepatic bile duct', 'neoplasm of extrahepatic bile duct', 'tumor of extrahepatic bile duct', 'extrahepatic bile duct tumor', 'extrahepatic bile duct tumour', 'extrahepatic bile duct neoplasm (disease)', 'tumor of the extrahepatic bile duct', 'tumour of extrahepatic bile duct']",,,,C0345913,,C4441,,,,,,
mondo:0021386,neoplasm of mediastinum,"['neoplasm of mediastinum', 'mediastinum neoplasm (disease)', 'tumour of mediastinum', 'mediastinal neoplasm', 'mediastinal tumor', 'mediastinum tumour', 'neoplasm of the mediastinum', 'tumor of the mediastinum', 'tumour of the mediastinum', 'mediastinal tumour', 'mediastinum tumor', 'tumor of mediastinum']",,,,,,C3221,,,239.89,,,
mondo:0021388,neoplasm of chest wall,"['neoplasm of chest wall', 'chest wall tumor', 'chest wall neoplasm (disease)', 'chest wall neoplasm', 'tumour of chest wall', 'tumour of the chest wall', 'tumor of chest wall', 'tumor of the chest wall', 'neoplasm of the chest wall', 'chest wall tumour']",,,,C1290309,,C4929,,,239.89,,,
mondo:0021389,neoplasm of aortic body,"['tumour of aortic body', 'tumour of the aortic body', 'aortic body neoplasm (disease)', 'paraganglioma of the aortic body', 'aortic body paraganglioma', 'neoplasm of aortic body', 'tumor of aortic body', 'tumor of the aortic body', 'aortic body neoplasm', 'aorticopulmonary paraganglioma', 'paraganglioma of aortic body', 'aortic body tumour', 'aortic body tumor', 'neoplasm of the aortic body']",,,,C0334417,,C4218,,,239.7,,,
mondo:0021390,polyp of ureter,"['ureteral polyp', 'ureter polyp', 'polyp of the ureter']",,,,C0346269,,C4530,,,593.89,,,
mondo:0021392,polyp of large intestine,"['polyp of the large intestine', 'large bowel polyp', 'colorectal polyp', 'polyp of the large bowel', 'polyp of large bowel', 'large intestine polyp']",,,,C0949059,,C5679,,,,,,
mondo:0021394,polyp of vagina,"['polyp, vaginal, benign', 'vagina polyp', 'vaginal polyp', 'polyp of the vagina']",,,,C0156390,,C3664,,,623.7,N84.2,,
mondo:0021396,polyp of vulva,"['vulva polyp', 'polyp of the vulva', 'vulvar polyp', 'mammalian vulva polyp']",,,,C0269218,,C3978,,,624.6,N84.3,,
mondo:0021398,polyp of rectum,"['polyp of the rectum', 'rectum polyp', 'rectal polyp']",,,,C0034887,,C3351,,,,,,
mondo:0021400,polyp of colon,"['colonic polyp', 'colon polyp', 'polyp of the colon']",,,,,,C2954,,D003111,,K63.5,,
mondo:0021402,polyp of external auditory canal,"['polyp of the external auditory canal', 'external auditory canal polyp', 'external acoustic meatus polyp', 'external Ear polyp']",,,,C0339765,,C4366,,,,,,
mondo:0021404,polyp of sphenoidal sinus,"['sphenoidal sinus polyp', 'polyp of the sphenoid sinus', 'polyp of the sphenoidal sinus', 'sphenoid sinus polyp', 'polyp of sphenoid sinus']",,,,C0264255,,C3933,,,471.8,,,
mondo:0021408,polyp of frontal sinus,"['polyp of the frontal sinus', 'frontal sinus polyp']",,,,C0339814,,C4367,,,471.8,,,
mondo:0021412,polyp of maxillary sinus,"['polyp of the maxillary sinus', 'maxillary antral polyp', 'maxillary sinus polyp']",,,,C0264239,,C3931,,,471.8,,,
mondo:0021416,polyp of gallbladder,"['gall bladder polyp', 'gallbladder polyp', 'polyp of the gallbladder']",,,,C0262493,,C3909,,,,,,
mondo:0021418,polyp of ethmoidal sinus,"['polyp of the ethmoid sinus', 'ethmoidal sinus polyp', 'ethmoidal polyp', 'ethmoid sinus polyp', 'polyp of the ethmoidal sinus', 'polyp of ethmoid sinus']",,,,C0264248,,C3932,,,471.8,,,
mondo:0021420,polyp of vocal cord,"['laryngeal vocal fold polyp', 'vocal cord polyp', 'polyp of the vocal cord']",,,,C0042929,,C3440,,,,,,
mondo:0021424,hemangiopericytoma of skin,"['hemangiopericytoma of the skin', 'zone of skin hemangiopericytoma', 'skin hemangiopericytoma']",,,,C0346084,,C4492,,,,,,
mondo:0021427,squamous cell carcinoma of lip,"['scc of Lip', 'squamous cell carcinoma of the Lip', 'lip squamous cell carcinoma', 'scc of the Lip', 'lip scc']",,,502366,C0280302,,C4042,,,,,,
mondo:0021429,squamous cell carcinoma of floor of mouth,"['scc of the floor of mouth', 'mouth floor squamous cell carcinoma', 'squamous cell carcinoma of the floor of mouth', 'scc of floor of mouth', 'floor of mouth scc', 'floor of mouth squamous cell carcinoma']",,,,C0280300,,C4041,,,,,,
mondo:0021431,squamous cell carcinoma of buccal mucosa,"['scc of buccal mucosa', 'buccal mucosa squamous cell carcinoma', 'scc of the buccal mucosa', 'squamous cell carcinoma of the buccal mucosa']",,,,C0280299,,C4040,,,,,,
mondo:0021437,lipoma of stomach,"['lipoma of the stomach', 'stomach lipoma', 'gastric lipoma']",,,,C1333777,,C5258,,,,,,
mondo:0021439,benign neoplasm of pituitary gland,"['benign tumour of the pituitary gland', 'benign tumor of pituitary', 'benign tumor of pituitary gland', 'pituitary tumor, benign', 'benign tumour of pituitary', 'benign neoplasm of the pituitary gland', 'benign pituitary tumour', 'benign tumour of pituitary gland', 'benign tumor of the pituitary gland', 'pituitary neoplasms, benign', 'benign pituitary tumor', 'benign pituitary gland tumour', 'benign pituitary neoplasm', 'benign tumor of the pituitary', 'pituitary gland benign neoplasm', 'benign neoplasm of the pituitary', 'benign pituitary gland neoplasm', 'benign pituitary gland tumor', 'benign neoplasm of pituitary', 'benign tumour of the pituitary']",60009,,,C0496901,,C4782,,,,D35.2,,
mondo:0021440,benign neoplasm of skin,"['benign skin neoplasm', 'benign cutaneous neoplasm', 'benign skin tumor', 'benign skin tumour', 'benign cutaneous tumour', 'benign tumor of skin', 'benign cutaneous tumor', 'benign tumour of the skin', 'benign tumor of the skin', 'zone of skin benign neoplasm', 'skin neoplasms, benign', 'benign tumour of skin', 'benign neoplasm of the skin']",,,,C0004998,,C2896,,,216.9,,,
mondo:0021441,benign neoplasm of exocrine pancreas,"['benign exocrine pancreas neoplasm', 'benign exocrine pancreas tumor', 'exocrine pancreas benign neoplasm', 'benign exocrine pancreas tumour', 'benign neoplasm of the exocrine pancreas', 'benign exocrine pancreatic neoplasm', 'benign tumor of the exocrine pancreas', 'benign tumour of exocrine pancreas', 'benign tumour of the exocrine pancreas', 'benign tumor of exocrine pancreas']",0080781,,,C0347285,,C4613,,,,,,
mondo:0021443,benign neoplasm of lymph node,"['benign lymph node tumour', 'benign lymph node tumor', 'benign tumor of lymph node', 'benign lymph node neoplasm', 'benign neoplasm of the lymph node', 'benign tumour of lymph node', 'benign tumor of the lymph node', 'lymph node benign neoplasm', 'benign tumour of the lymph node']",0080617,,,C0154054,,C3636,,,229.0,,,
mondo:0021444,benign neoplasm of large intestine,"['benign tumour of the large intestine', 'benign tumour of large bowel', 'benign large bowel neoplasm', 'benign tumour of the large bowel', 'neoplasms, colorectal, benign', 'benign tumor of large intestine', 'benign neoplasm of the large intestine', 'benign colorectal tumour', 'benign colorectal tumors', 'benign large bowel tumour', 'benign large intestine tumor', 'tumors, colorectal, benign', 'benign large bowel tumor', 'benign tumor of the large intestine', 'benign colorectal neoplasm', 'benign colorectal tumours', 'benign neoplasm of large bowel', 'benign colorectal neoplasms', 'benign tumor of large bowel', 'large intestine benign neoplasm', 'benign tumour of large intestine', 'benign tumor of the large bowel', 'colorectal neoplasms, benign', 'colorectal tumors, benign', 'benign large intestine neoplasm', 'benign colorectal tumor', 'benign neoplasm of the large bowel', 'benign large intestine tumour']",,,,C0347272,,C4610,,,,,,
mondo:0003952,adult central nervous system choriocarcinoma,"['central nervous system choriocarcinoma', 'choriocarcinoma of adult CNS', 'adult central nervous system choriocarcinoma', 'choriocarcinoma of adult central nervous system', 'choriocarcinoma of the adult CNS', 'choriocarcinoma of the adult central nervous system', 'adult CNS choriocarcinoma', 'adult choriocarcinoma of the central nervous system', 'choriocarcinoma of the central nervous system of adults']",6634,,,C1370505,,C5793,,,,,,
mondo:0003953,pediatric CNS choriocarcinoma,"['choriocarcinoma of pediatric central nervous system', 'choriocarcinoma of the pediatric CNS', 'childhood central nervous system choriocarcinoma', 'choriocarcinoma of pediatric CNS', 'pediatric central nervous system choriocarcinoma', 'choriocarcinoma of the pediatric central nervous system', 'paediatric choriocarcinoma of the central nervous system', 'choriocarcinoma of the childhood CNS', 'choriocarcinoma of childhood central nervous system', 'paediatric central nervous system choriocarcinoma', 'pediatric choriocarcinoma of the central nervous system', 'choriocarcinoma of paediatric central nervous system', 'childhood CNS choriocarcinoma', 'choriocarcinoma of the central nervous system of childhood', 'choriocarcinoma of paediatric CNS', 'choriocarcinoma of the paediatric CNS', 'childhood choriocarcinoma of the central nervous system', 'Central nervous system choriocarcinoma', 'choriocarcinoma of the paediatric central nervous system', 'choriocarcinoma of the childhood central nervous system', 'choriocarcinoma of childhood CNS']",6639,,,C1377604,,C6206,,,,,,
mondo:0003954,angiokeratoma of Fordyce,"['Fordyce angiokeratoma', 'Fordyce-type angiokeratoma of scrotum', 'Fordyce^s spot']",664,,,C0263639,,,,,,,,
mondo:0003955,juvenile breast papillomatosis,"['juvenile breast papillomatosis', 'juvenile papillomatosis of breast', 'breast juvenile papillomatosis', 'juvenile papillomatosis of the breast', 'Swiss cheese disease']",6641,,,C1334303,,C9503,,,,,,
mondo:0003956,Baastrup syndrome,"['Baastrup^s syndrome', 'Baastrup syndrome', 'kissing spine']",6643,,,C0158248,,,,,721.5,,,
mondo:0003957,adult pineoblastoma,"['pineoblastoma of adults', 'adult pineoblastoma', 'pineoblastoma']",6648,,,C0281332,,C8292,,,,,,
mondo:0003958,childhood central nervous system immature teratoma,"['childhood central nervous system immature teratoma', 'pediatric central nervous system immature teratoma', 'paediatric central nervous system immature teratoma', 'central nervous system immature teratoma of childhood']",6654,,,C1332954,,C27405,,,,,,
mondo:0003959,breast large cell neuroendocrine carcinoma,"['large cell neuroendocrine carcinoma of breast', 'breast large cell neuroendocrine carcinoma']",6657,,,C1511316,,C40356,,,,,,
mondo:0003960,pulmonary large cell neuroendocrine carcinoma,"['large cell lung neuroendocrine carcinoma', 'large cell neuroendocrine carcinoma of lung', 'LCNEC of the lung', 'large cell lung carcinoma with neuroendocrine differentiation', 'large cell neuroendocrine carcinoma of the lung', 'lung large cell neuroendocrine carcinoma', 'pulmonary large cell neuroendocrine carcinoma']",6658,,,C1334363,,C5672,,,,,,
mondo:0003962,Froelich syndrome,"['dystrophia Adiposogenitalis', 'Froelich^s adiposity', 'Frohlich syndrome', 'Launois-Cleret syndrome', 'adiposogenital syndrome', 'Frohlich^s syndrome', 'Frolich^s syndrome', 'Babinski-Froelich syndrome', 'Froehlich syndrome', 'Froehlich^s syndrome', 'hypothalamic infantilism-obesity', 'Fröhlich syndrome', 'adiposogenital dystrophy', 'Froelich^s syndrome', 'Adiposodysgenesis', 'sexual infantilism']",6676,,,,,C34625,,,253.8,,,
mondo:0003963,diffuse infiltrative lymphocytosis syndrome,"['diffuse infiltra. lymph. sydrome', 'diffuse infiltra. lymph. syndrome']",6677,,,C1333292,,C35699,,,,,,
mondo:0003964,myositis ossificans,"['Myisitis ossificans', 'progressive ossifying myositis', 'ossification - muscle', 'myositis ossificans progressiva', 'progressive myositis ossificans', 'fibrodysplasia ossificans progressiva', 'FOP']",668,,,C0027122,,C3253,,D009221,,,,
mondo:0003965,Capgras syndrome,['Capgras delusion theory'],6680,,,,,C34446,,D002194,,,,
mondo:0003966,testicular monophasic choriocarcinoma,,6693,,,C1515290,,C39935,,,,,,
mondo:0003967,synchronous multifocal osteogenic sarcoma,['synchronous multifocal osteosarcoma'],6696,,,C1336544,,C6471,,,,,,
mondo:0003968,asynchronous multifocal osteogenic sarcoma,['asynchronous multifocal osteosarcoma'],6697,,,C1332342,,C6472,,,,,,
mondo:0003969,amphetamine abuse,,670,,,,,,,D019969,305.70,,,
mondo:0003970,gastric fundus carcinoma,"['carcinoma of gastric fundus', 'cancer of gastric fundus', 'gastric fundus (stomach) cancer', 'fundus of stomach carcinoma', 'carcinoma of the fundus of the stomach', 'cancer of the gastric fundus', 'carcinoma of fundus of stomach', 'cancer of fundus of stomach', 'cancer of the fundus of the stomach', 'gastric fundus cancer', 'carcinoma of the gastric fundus']",6700,,,C0345799,,C8398,,,,,,
mondo:0003971,gastric pylorus carcinoma,"['gastric pylorus carcinoma', 'carcinoma of pylorus of stomach', 'gastric pylorus (stomach) cancer', 'carcinoma of gastric pylorus', 'gastric pylorus cancer', 'cancer of the pylorus of the stomach', 'carcinoma of the gastric pylorus', 'cancer of the gastric pylorus', 'cancer of gastric pylorus', 'cancer of pylorus of stomach', 'carcinoma of the pylorus of the stomach']",6703,,,C1333787,,C6795,,,,,,
mondo:0003972,gastric body carcinoma,"['carcinoma of body of stomach', 'gastric body cancer', 'cancer of gastric body', 'carcinoma of the body of the stomach', 'cancer of the body of the stomach', 'cancer of the gastric body', 'cancer of body of stomach', 'body of stomach carcinoma', 'carcinoma of gastric body', 'gastric body carcinoma', 'gastric body (stomach) cancer', 'carcinoma of the gastric body']",6705,,,C0345804,,C8399,,,,,,
mondo:0003973,tubular variant testicular seminoma,"['testicular seminoma, tubular variant']",6706,,,C1515294,,C40959,,,,,,
mondo:0003975,Littre gland carcinoma,"['carcinoma of male urethral gland', 'carcinoma of Littre glands', 'male urethral gland carcinoma', 'carcinoma of LittrC) glands', 'carcinoma of Littré glands']",6721,,,C1516285,,C39865,,,,,,
mondo:0003976,malignant type AB thymoma,"['malignant type AB thymoma', 'thymoma, mixed type, malignant', 'thymoma type AB, malignant']",6723,,,C1266093,,C6886,,,,,,
mondo:0003978,colon small cell neuroendocrine carcinoma,"['small cell colon carcinoma', 'small cell carcinoma of the colon', 'Oat cell colon carcinoma', 'colonic small cell carcinoma', 'colon small cell neuroendocrine cancer', 'Oat cell carcinoma of the colon', 'Oat cell carcinoma of colon', 'small cell carcinoma of colon', 'colon Oat cell carcinoma', 'colon small cell carcinoma', 'colon small cell neuroendocrine carcinoma', 'colonic Oat cell carcinoma']",6727,,,C1333099,,C6761,,,,,,
mondo:0003979,intrahepatic bile duct cystadenoma,"['intrahepatic bile duct mucinous cystic neoplasm', 'cystadenoma of the intrahepatic bile duct', 'intrahepatic bile duct cystadenoma']",6733,,,C1334257,,C96835,,,,,,
mondo:0003980,schwannoma of jugular foramen,"['jugular foramen schwannoma', 'schwannoma of the jugular Foramen', 'neurilemmoma of the jugular Foramen', 'neurilemmoma of jugular Foramen', 'jugular Foramen neurilemmoma']",6735,,,C1334300,,C5323,,,,,,
mondo:0003982,bilateral breast carcinoma,"['bilateral breast carcinoma', 'bilateral breast cancer']",6741,,,C0281267,,C8287,,,,,,
mondo:0003983,synchronous bilateral breast carcinoma,,6742,,,C1515107,,C40370,,,,,,
mondo:0003984,internal auditory canal lipoma,"['lipoma of internal acoustic meatus', 'inner Ear lipoma', 'internal Ear lipoma', 'internal acoustic meatus lipoma', 'lipoma of internal auditory canal', 'lipoma of the internal auditory canal']",6752,,,C1334226,,C5452,,,,,,
mondo:0003985,chest wall lymphoma,"['lymphoma of the chest wall', 'chest wall cancer', 'malignant tumour of chest wall', 'primary chest wall lymphoma', 'chest wall lymphoma', 'lymphoma of chest wall']",6758,,,C1332933,,C6712,,,,,,
mondo:0003987,lung lymphoma,"['lymphoma of the lung', 'lung lymphoma', 'primary lung lymphoma', 'lymphoma of lung', 'pulmonary lymphoma']",6760,,,C1704383,,C4794,,,,,,
mondo:0003988,sternum lymphoma,"['lymphoma of sternum', 'sternum lymphoma', 'primary sternal lymphoma', 'lymphoma of the sternum', 'sternal lymphoma']",6762,,,C1336504,,C6716,,,,,,
mondo:0003989,polyembryoma of the ovary,"['ovarian polyembryoma', 'polyembryoma']",6774,,,C1514199,,C39990,,,,,,
mondo:0003990,malignant breast myoepithelioma,"['breast malignant myoepithelioma', 'malignant breast myoepithelioma', 'breast myoepithelial carcinoma']",6776,,,C1518167,,C40395,,,,,,
mondo:0003991,villoglandular endometrial endometrioid adenocarcinoma,['villoglandular endometrial endometrioid adenocarcinoma'],6777,,,C1336962,,C27846,,,,,,
mondo:0003992,childhood botryoid rhabdomyosarcoma,"['childhood sarcoma Botryoides', 'childhood botryoid-type embryonal rhabdomyosarcoma', 'paediatric botryoid rhabdomyosarcoma', 'pediatric botryoid rhabdomyosarcoma', 'botryoid rhabdomyosarcoma of childhood', 'botryoid-type embryonal rhabdomyosarcoma']",6786,,,C1332944,,C35574,,,,,,
mondo:0003993,childhood vagina botryoid rhabdomyosarcoma,"['childhood botryoid-type embryonal rhabdomyosarcoma of the vagina', 'botryoid-type embryonal rhabdomyosarcoma of the vagina of childhood', 'vaginal childhood botryoid-type embryonal rhabdomyosarcoma', 'pediatric botryoid-type embryonal rhabdomyosarcoma of the vagina', 'paediatric botryoid-type embryonal rhabdomyosarcoma of the vagina', 'childhood sarcoma Botryoides of the vagina', 'vaginal childhood sarcoma Botryoides']",6787,,,C1332945,,C35556,,,,,,
mondo:0003994,botryoid-type embryonal rhabdomyosarcoma of the vagina,"['sarcoma Botryoides of the vagina', 'botryoid-type embryonal rhabdomyosarcoma of the vagina', 'botryoid rhabdomyosarcoma of vagina', 'vagina botryoid rhabdomyosarcoma']",6788,,,C1511275,,C40268,,,,,,
mondo:0003995,vulvar childhood botryoid-type embryonal rhabdomyosarcoma,"['mammalian vulva childhood botryoid rhabdomyosarcoma', 'childhood botryoid rhabdomyosarcoma of mammalian vulva', 'vulvar childhood botryoid-type embryonal rhabdomyosarcoma', 'childhood botryoid-type embryonal rhabdomyosarcoma of the vulva', 'childhood sarcoma Botryoides of the vulva']",6789,,,C1332946,,C36098,,,,,,
mondo:0003996,basal ganglia disorder,"['collection of basal ganglia disease or disorder', 'disorder of collection of basal ganglia', 'collection of basal ganglia disease', 'disease of collection of basal ganglia', 'basal ganglia disease', 'disease of basal ganglia', 'disorder of basal ganglia']",679,,,C0004782,,,,D001480,333.0,,,
mondo:0003997,colon Kaposi sarcoma,"['colonic Kaposi^s sarcoma', 'colonic Kaposis sarcoma', 'Kaposi^s sarcoma of colon', 'Kaposi^s sarcoma of the colon', 'colon Kaposi sarcoma', 'colon Kaposi^s sarcoma', 'colon Kaposis sarcoma', 'colon Kaposi^s sarcoma (disease)', 'colonic Kaposi sarcoma']",6804,,,C1333091,,C5516,,,,,,
mondo:0003999,juvenile pilocytic astrocytoma,['juvenile pilocytic astrocytoma'],6811,,,C0280783,,C27081,,,,,,
mondo:0004000,childhood pilocytic astrocytoma,"['pilocytic astrocytoma of childhood', 'pilocytic astrocytoma', 'childhood pilocytic astrocytoma', 'pediatric pilocytic astrocytoma', 'paediatric pilocytic astrocytoma']",6812,,,C1332995,,C4048,,,,,,
mondo:0004001,compartment syndrome,"['compartmental syndrome', 'compartment syndrome']",682,,,C0009492,,C118422,,D003161,958.90,,,
mondo:0004004,motor nerve neuritis,['motor neuritis'],683,,,C0235025,,C3500,,D009443,,,,
mondo:0004005,rete ovarii adenoma,"['adenoma, rete ovarii, benign', 'rete ovarii adenoma']",6837,,,C1514905,,C40018,,,,,,
mondo:0004006,rete ovarii cystadenofibroma,"['cystadenofibroma of rete ovarii', 'rete ovarii cystadenofibroma']",6838,,,C1514906,,C40020,,,,,,
mondo:0004007,breast intraductal proliferative lesion,"['ductal intraepithelial neoplasia', 'mammary intraepithelial neoplasia, ductal type', 'DIN', 'intraductal proliferative lesion', 'intraductal proliferative lesion of the breast']",6839,,,C1334631,,C27942,,,,,,
mondo:0004008,flat ductal epithelial atypia,"['FEA', 'flat ductal epithelial atypia of the breast', 'DIN 1A', 'flat epithelial atypia of the breast', 'flat ductal epithelial atypia', 'flat epithelial atypia', 'ductal intraepithelial neoplasia, grade 1A', 'clinging carcinoma']",6841,,,C1333620,,C36086,,,,,,
mondo:0004009,kidney pelvis sarcomatoid transitional cell carcinoma,"['renal pelvis sarcomatoid transitional cell carcinoma', 'infiltrating renal pelvis urothelial carcinoma, sarcomatoid variant', 'sarcomatoid transitional cell carcinoma of renal pelvis', 'sarcomatoid transitional cell carcinoma of the renal pelvis', 'sarcomatoid transitional cell carcinoma of kidney pelvis', 'kidney pelvis sarcomatoid transitional cell carcinoma', 'sarcomatoid transitional cell carcinoma of the kidney pelvis']",6844,,,C1335752,,C6186,,,,,,
mondo:0004010,infiltrating renal pelvis/ureter urothelial carcinoma,"['infiltrating ureter transitional cell carcinoma', 'infiltrating renal pelvis and ureter urothelial carcinoma', 'infiltrating renal pelvis and ureter transitional cell carcinoma']",,,,C1512750,,C39879,,,,,,
mondo:0004012,adult botryoid rhabdomyosarcoma,"['botryoid rhabdomyosarcoma of adults', 'adult botryoid sarcoma', 'adult botryoid-type embryonal rhabdomyosarcoma']",6847,,,C1332185,,C36099,,,,,,
mondo:0004013,adult vagina botryoid embryonal rhabdomyosarcoma,"['adult vagina botryoid rhabdomyosarcoma', 'botryoid-type embryonal rhabdomyosarcoma of the vagina of adults', 'adult botryoid-type embryonal rhabdomyosarcoma of the vagina', 'adult sarcoma Botryoides of the vagina']",6848,,,C1515893,,C40267,,,,,,
mondo:0004014,ethmoid sinus ectopic meningioma,"['primary ectopic meningioma of the ethmoid sinus', 'ethmoid sinus primary ectopic meningioma', 'primary ectopic meningioma of ethmoidal sinus', 'primary ectopic meningioma of the ethmoidal sinus', 'primary ectopic meningioma of ethmoid sinus', 'ethmoidal sinus primary ectopic meningioma']",6854,,,C1333475,,C5309,,,,,,
mondo:0004015,pineal region teratoma,"['teratoma of pineal area', 'teratoma of pineal region', 'teratoma of the pineal region', 'teratoma of the pineal area', 'pineal area teratoma']",6856,,,C1335419,,C6753,,,,,,
mondo:0004016,pineal region mature teratoma,"['mature teratoma of the pineal area', 'mature teratoma of pineal region', 'mature teratoma of the pineal region', 'pineal area mature teratoma', 'mature teratoma of pineal area']",6857,,,C1335417,,C6754,,,,,,
mondo:0004017,pineal region immature teratoma,"['immature teratoma of the pineal region', 'immature teratoma of pineal region', 'atypical pineal teratoma', 'immature teratoma of the pineal area', 'immature teratoma of pineal area', 'pineal area immature teratoma']",6858,,,C1335416,,C6755,,,,,,
mondo:0004019,oxyphilic endometrial endometrioid adenocarcinoma,['oxyphilic endometrial endometrioid adenocarcinoma'],6865,,,C1518768,,C27849,,,,,,
mondo:0004020,mediastinal gray zone lymphoma,"['mediastinal B-cell lymphoma, unclassifiable, with features Intermediate between diffuse large B-cell lymphoma and Classic Hodgkin lymphoma', 'mediastinal B-cell lymphoma, unclassifiable, with features Intermediate between diffuse large B-cell lymphoma and classical Hodgkin lymphoma', 'mediastinal Grey zone lymphoma', 'mediastinal Gray zone lymphoma']",6867,,,C1334657,,C37870,,,,,,
mondo:0004021,mediastinal malignant lymphoma,"['lymphoma of the mediastinum', 'primary mediastinal lymphoma', 'mediastinal lymphoma', 'lymphoma of mediastinum', 'mediastinum lymphoma', 'mediastinal malignant lymphoma']",6868,,,C1334665,,C6633,,,,,,
mondo:0004022,parasagittal meningioma,,6869,,,C0751304,,C4960,,,,,,
mondo:0004024,spinal cord neuroblastoma,"['neuroblastoma of spinal cord', 'neuroblastoma of the spinal cord', 'spinal cord neuroblastoma']",6871,,,C1336046,,C5155,,,,,,
mondo:0004026,skin tag,"['fibroepithelial polyp of the skin', 'fibroepithelial polyp of skin', 'acrochordon', 'fibroma molle', 'fibroepithelial polyp', 'soft fibroma', 'cutaneous tag', 'cutaneous fibroepithelial polyp']",6873,,,C0037293,,C3374,,,,,,
mondo:0004028,small intestinal fibrosarcoma,"['small intestine fibrosarcoma (disease)', 'small intestinal fibrosarcoma', 'fibrosarcoma of small intestine', 'small bowel fibrosarcoma', 'fibrosarcoma, small intestine', 'fibrosarcoma of small bowel', 'fibrosarcoma of the small intestine', 'fibrosarcoma of the small bowel', 'small intestine fibrosarcoma']",6880,,,C1335994,,C5336,,,,,,
mondo:0004030,ureter transitional cell carcinoma,"['ureteral urothelial cell carcinoma', 'ureter urothelial carcinoma', 'transitional cell carcinoma of the ureter', 'transitional cell carcinoma of ureter', 'ureteral transitional cell carcinoma', 'urothelial cell carcinoma of ureter', 'ureter urothelial cancer', 'urothelial cell carcinoma of the ureter', 'ureter transitional cell carcinoma']",6888,,,C0577692,,C4830,1001973,,,,,
mondo:0004031,ovary mixed epithelial carcinoma,"['mixed ovarian carcinoma', 'mixed epithelial carcinoma of ovary']",6898,,,,,,,,,,,
mondo:0004032,ovarian seromucinous carcinoma,"['malignant ovarian mixed epithelial neoplasm', 'ovarian mixed epithelial carcinoma', 'mixed epithelial carcinoma of the ovary', 'mixed epithelial carcinoma of ovary', 'malignant ovarian mixed epithelial tumour', 'malignant ovarian mixed epithelial tumor', 'ovarian Seromucinous carcinoma']",6899,,,C1518232,,C40090,1000358,,,,,
mondo:0004034,eye lymphoma,"['primary eye lymphoma', 'eye lymphoma', 'eyeball of camera-type eye lymphoma', 'lymphoma of eyeball of camera-type eye']",6903,,,C1333519,,C35690,,,,,,
mondo:0004035,glomangiomatosis,,6906,,,C1333824,,C27496,,,,,,
mondo:0004037,retinal edema,,6929,,,,,,,D010211,362.83,,,
mondo:0004038,dental enamel hypoplasia,['enamel hypoplasia'],693,,,C0011351,,C34529,1001304,D003744,,,,
mondo:0004039,papillary extrahepatic bile duct adenocarcinoma,,6931,,,,,,,,,,,
mondo:0004040,urinary bladder inverted papilloma,"['bladder inverted papilloma', 'urinary bladder inverted papilloma']",6932,,,C1511190,,C39859,,,,,,
mondo:0004041,urothelial papilloma,"['uPA', 'transitional cell papilloma of bladder', 'bladder papilloma', 'urothelial papilloma', 'bladder transitional cell papilloma']",6933,,,,,C3842,,,,,,
mondo:0004042,urethra inverted papilloma,"['urethral inverted papilloma', 'urethra inverted papilloma', 'inverted papilloma of the urethra', 'inverted papilloma of urethra']",6934,,,C1336887,,C6173,,,,,,
mondo:0004043,ureter inverted papilloma,"['ureter inverted papilloma', 'ureteral inverted papilloma', 'inverted papilloma of ureter', 'inverted papilloma of the ureter']",6935,,,C1336874,,C6174,,,,,,
mondo:0004044,ureter urothelial papilloma,['ureter urothelial papilloma'],6936,,,C1519823,,C6160,,,,,,
mondo:0004045,pediatric intraocular retinoblastoma,"['pediatric intraocular retinoblastoma', 'intraocular retinoblastoma', 'childhood intraocular retinoblastoma', 'intraocular retinoblastoma of childhood']",6938,,,C1321869,,C9047,,,,,,
mondo:0003913,choroid mixed cell melanoma,"['optic choroid mixed cell uveal melanoma', 'mixed cell uveal melanoma of optic choroid', 'choroid mixed cell melanoma']",6525,,,C1333025,,C35782,,,,,,
mondo:0003915,cortical thymoma,"['thymoma, cortical', 'cortical thymoma', 'thymoma type B2', 'polygonal cell thymoma']",6530,,,C1266095,,C6888,,,,,,
mondo:0003916,overnutrition,,654,,,C1257763,,,,D044343,278.8,,,
mondo:0003917,heart lymphoma,"['lymphoma of the heart', 'Primary heart lymphoma', 'lymphoma of heart', 'heart lymphoma', 'Cardiac lymphoma', 'primary Cardiac lymphoma', 'PCL']",6547,,,C1332850,,C5368,,,,,,
mondo:0003918,angiomatous meningioma,['angiomatous meningioma (morphologic abnormality)'],6548,,,C0334608,,C4332,1000086,,,,,
mondo:0003921,posterior foramen magnum meningioma,"['meningioma of the posterior Foramen magnum', 'meningioma of posterior Foramen magnum']",6553,,,C1335449,,C5282,,,,,,
mondo:0003922,ovarian clear cell malignant adenofibroma,"['ovarian clear cell malignant adenofibroma', 'ovarian clear cell adenocarcinofibroma']",6554,,,C2075522,,C40079,,,,,,
mondo:0003923,ethmoid sinus Schneiderian papilloma,"['Schneiderian papilloma of ethmoid sinus', 'Schneiderian papilloma of the ethmoid sinus', 'ethmoid sinus Schneiderian papilloma']",6559,,,C1333476,,C6836,,,,,,
mondo:0003924,adrenal cortex adenoma,"['adrenal cortical adenoma', 'benign adrenal adenoma', 'benign adrenal gland adenoma', 'benign adenoma of adrenal gland', 'adenoma, adrenocortical, benign', 'adrenal adenoma', 'adrenocortical adenoma', 'cortical cell adenoma', 'benign adenoma of the adrenal gland', 'adrenal cortex adenoma', 'adenoma of adrenal gland', 'adenoma of the adrenal gland', 'adrenal incidentaloma', 'adenoma of the adrenal cortex', 'adrenal gland adenoma', 'adenoma of adrenal cortex']",656,,99888,C0206667,,C9003,0003104,D018246,,,,0008256
mondo:0003925,ethmoid sinus inverted papilloma,"['inverted papilloma of ethmoid sinus', 'inverted papilloma of the ethmoid sinus', 'ethmoid sinus inverted papilloma']",6562,,,C1333474,,C6843,,,,,,
mondo:0003926,neurilemmoma of the pleura,"['neurilemmoma of pleura', 'pleural neurilemmoma', 'schwannoma of pleura', 'schwannoma of the pleura', 'pleura schwannoma', 'pleural schwannoma']",6564,,,C1335435,,C5418,,,,,,
mondo:0003927,posterior uveal melanoma,"['small size posterior uveal melanoma', 'medium/large size posterior uveal melanoma']",6566,,,,,,,,,,,
mondo:0003928,uterine corpus myxoid leiomyosarcoma,"['uterine corpus myxoid leiomyosarcoma', 'uterine myxoid leiomyosarcoma', 'myxoid leiomyosarcoma of body of uterus', 'body of uterus myxoid leiomyosarcoma']",6567,,,C1519861,,C40175,,,,,,
mondo:0003929,vestibular micropapillomatosis,"['vestibular micropapillomatosis', 'micropapillomatosis labialis']",6569,,,C1519982,,C40290,,,,,,
mondo:0003930,non-invasive bladder urothelial carcinoma,"['stage 0 bladder urothelial cancer', 'stage 0 transitional cell carcinoma of urinary bladder', 'stage 0 transitional cell carcinoma of the urinary bladder', 'stage 0 urinary bladder transitional cell carcinoma', 'non-invasive bladder urothelial carcinoma', 'stage 0 bladder urothelial carcinoma', 'stage 0 bladder urothelial carcinoma aJCC v7', 'stage 0 transitional cell carcinoma of bladder', 'stage 0 bladder urothelial carcinoma aJCC v6 and v7', 'stage 0 bladder urothelial carcinoma aJCC v6', 'stage 0 transitional cell carcinoma of the bladder']",6571,,,C1336089,,C6188,,,,,,
mondo:0003931,childhood optic tract astrocytoma,"['pediatric optic tract astrocytoma', 'optic tract astrocytoma of childhood', 'pediatric visual pathway astrocytoma', 'paediatric visual pathway astrocytoma', 'childhood visual pathway astrocytoma', 'paediatric optic tract astrocytoma', 'childhood optic tract astrocytoma']",6575,,,C1333014,,C7534,,,,,,
mondo:0003932,childhood optic nerve glioma,"['paediatric optic nerve glioma', 'optic nerve glioma of childhood', 'paediatric visual pathway glioma', 'visual pathway and hypothalamic glioma, childhood', 'pediatric optic nerve glioma', 'pediatric optic tract glioma', 'visual pathway glioma', 'glioma of paediatric visual pathway', 'glioma of the paediatric visual pathway', 'childhood visual pathway glioma', 'glioma of childhood visual pathway', 'glioma of the childhood visual pathway', 'pediatric visual pathway glioma', 'paediatric optic tract glioma', 'childhood optic tract glioma', 'glioma of the pediatric visual pathway', 'glioma of pediatric visual pathway']",6576,,,,,C7535,,,,,,
mondo:0003933,chest wall bone cancer,"['malignant bone neoplasm of chest wall', 'malignant chest wall bone neoplasm', 'malignant bone tumour of chest wall', 'malignant chest wall bone tumor', 'malignant bone tumour of the chest wall', 'chest wall bone cancer', 'malignant bone neoplasm of the chest wall', 'bone cancer of chest wall', 'malignant bone tumor of chest wall', 'malignant chest wall bone tumour', 'malignant bone tumor of the chest wall']",6579,,,C1334572,,C6724,,,,,,
mondo:0003934,breast apocrine carcinoma,"['apocrine breast carcinoma', 'breast apocrine carcinoma', 'apocrine carcinoma of breast', 'apocrine carcinoma of the breast', 'apocrine adenocarcinoma of breast', 'breast apocrine adenocarcinoma']",6581,,,C1332316,,C5141,,,,,,
mondo:0003935,oncocytic breast carcinoma,['oncocytic breast carcinoma'],6585,,,C1518574,,C40366,,,,,,
mondo:0003936,invasive tubular breast carcinoma,"['invasive tubular carcinoma of the breast', 'invasive tubular breast carcinoma', 'tubular carcinoma of the breast', 'breast tubular adenocarcinoma', 'tubular breast carcinoma', 'tubular carcinoma of breast', 'infiltrating tubular carcinoma of breast', 'infiltrating tubular breast carcinoma', 'tubular breast cancer', 'invasive tubular carcinoma of breast', 'infiltrating tubular carcinoma of the breast']",6587,,,C1328544,,C9135,,,,,,
mondo:0003937,spondylitis,['vertebra inflammation'],6590,,,,,C116779,,D013166,720.89,,,
mondo:0003938,bladder colonic type adenocarcinoma,"['bladder colonic type adenocarcinoma', 'bladder enteric type adenocarcinoma']",6594,,,C1511188,,C39835,,,,,,
mondo:0003939,muscle tissue disorder,"['muscle organ disease or disorder', 'disease of muscle tissue', 'muscle tissue disease or disorder', 'muscle tissue disease', 'muscle organ disease', 'disorder of muscle organ', 'disease of muscle organ', 'muscular disorder', 'disorder of muscle tissue']",66,,,,,,0002970,D009135,,M60-M63,,
mondo:0003940,Kummell disease,"['bony vertebral centrum osteonecrosis', 'avascular necrosis of a vertebral body', 'Kummell^s spondylitis', 'traumatic spondylopathy', 'Kummell disease', 'Kummell^s disease', 'osteonecrosis of bony vertebral centrum']",6603,,,C0152088,,,,,721.7,M48.3,,
mondo:0003941,classic variant of chromophobe renal cell carcinoma,['classic variant of chromophobe renal cell carcinoma'],6605,,,C1333062,,C27888,,,,,,
mondo:0003942,eosinophilic variant of chromophobe renal cell carcinoma,['eosinophilic variant of chromophobe renal cell carcinoma'],6606,,,C1333405,,C27889,,,,,,
mondo:0003943,central nervous system hibernoma,"['hibernoma of nervous system', 'hibernoma of the central nervous system', 'hibernoma of central nervous system', 'nervous system hibernoma', 'central nervous system hibernoma']",6607,,,C1708362,,C6997,,,,,,
mondo:0003944,endobronchial leiomyoma,"['lung leiomyoma of bronchus', 'endobronchial leiomyoma', 'bronchus lung leiomyoma']",6608,,,C1333386,,C5661,,,,,,
mondo:0003945,bone epithelioid hemangioma,"['bone hemangioma', 'osseous epithelioid hemangioma', 'osseous epithelioid angioma', 'epithelioid hemangioma of bone', 'hemangioma of bone', 'bone epithelioid angioma', 'bone epithelioid hemangioma', 'epithelioid angioma of the bone', 'epithelioid angioma of bone', 'osseous hemangioma', 'epithelioid hemangioma of the bone']",6610,,,C1332578,,C5396,1000132,,,,,
mondo:0003946,vaginal villous adenoma,"['vagina villous adenoma', 'vaginal villous adenoma']",6613,,,C1519936,,C40259,,,,,,
mondo:0003947,hyper-IgM syndrome,"['immunodeficiency with hyper-IgM', 'hyperimmunoglobulin M syndrome']",0080544,,,C0272236,,C84783,,D053306,279.05,,,
mondo:0003948,cerebral hemangioma,"['cerebral hemispheric angioma', 'angioma of cerebrum', 'hemangioma of cerebral hemispheres', 'cerebral hemispheric hemangioma', 'cerebral hemangioma', 'hemangioma of the cerebral hemispheres', 'hemangioma of the cerebrum', 'cerebral angioma', 'angioma of the cerebrum', 'hemangioma of telencephalon', 'telencephalon hemangioma', 'hemangioma of cerebrum', 'angioma of the cerebral hemispheres', 'angioma of cerebral hemispheres']",6621,,,C0877388,,C5433,,,,,,
mondo:0003950,nipple carcinoma,"['carcinoma of nipple', 'nipple carcinoma', 'nipple cancer']",6629,,,C1334966,,C28432,,,,,,
mondo:0003951,scrotal hemangioma,"['angioma of scrotum', 'hemangioma of scrotum', 'scrotal hemangioma', 'angioma of the scrotum', 'hemangioma of the scrotum', 'scrotal angioma', 'scrotum hemangioma']",663,,,C1335936,,C6387,,,,,,
mondo:0012131,"metaphyseal undermodeling, spondylar dysplasia, and overgrowth","['overgrowth-metaphyseal undermodeling-spondylar dysplasia syndrome', 'metaphyseal undermodeling, spondylar dysplasia, and overgrowth']",,608811,498485,C1837316,,,,C537355,,,,
mondo:0012132,"colorectal cancer, susceptibility to, 1","['CRCS1', 'colorectal cancer, susceptibility to, on chromosome 9', 'colorectal cancer caused by mutation in GALNT12', 'colorectal cancer, susceptibility to, type 1', 'susceptibility to colorectal cancer 1', 'colorectal adenoma and cancer, susceptibility to', 'GALNT12 colorectal cancer', 'colorectal cancer, susceptibility to, 1']",,608812,,,,,,,,,,
mondo:0012133,"lateral semicircular canal malformation, familial, with external and middle ear abnormalities","['lateral semicircular canal malformation, familial, with external and middle ear abnormalities']",,608814,,C1837314,,,,C537879,,,,
mondo:0012134,"myoclonic epilepsy, juvenile, susceptibility to, 3","['EJM3', 'myoclonic epilepsy, juvenile, susceptibility to, 3', 'epilepsy, juvenile myoclonic 3']",0111326,608816,,C1837308,,,,,,,,
mondo:0012135,"restless legs syndrome, susceptibility to, 2","['RLS2', 'restless legs syndrome, susceptibility to, 2', 'restless legs syndrome 2']",,608831,,C1837285,,,,,,,,
mondo:0012136,"carnitine palmitoyl transferase II deficiency, neonatal form","['Cpt2 deficiency, lethal neonatal', 'CPT 2 deficiency, lethal neonatal', 'CPTII, lethal systemic form', 'Carnitine palmitoyl transferase II deficiency, lethal systemic form', 'Carnitine palmitoyl transferase deficiency type 2, lethal systemic form', 'Carnitine Palmitoyltransferase 2 deficiency, antenatal', 'Carnitine palmitoyl transferase deficiency type 2, neonatal form', 'Carnitine Palmitoyltransferase 2 deficiency, lethal neonatal', 'CPT2, neonatal form', 'CPT2, lethal systemic form', 'CARNITINE PALMITOYLTRANSFERASE II deficiency, lethal neonatal', 'CPT II deficiency, lethal neonatal', 'Carnitine Palmitoyltransferase 2 deficiency, neonatal', 'CPTII, neonatal form']",,608836,228308,C1833518,"['0.02246', '0.444', '-0.4019', '-0.1562', '0.10376', '-0.4883', '-0.08057', '0.1175', '-0.054', '-0.1903', '-0.325', '-0.6333', '-0.1499', '0.2725', '-0.596', '-0.5137', '-0.1351', '-0.1616', '-0.516', '-0.801', '0.312', '-0.1932', '0.992', '-0.673', '-0.3904', '-0.476', '-0.1775', '0.0842', '0.09216', '0.2438', '0.4111', '0.3914', '0.3835', '-0.1298', '-0.284', '-0.552', '0.0815', '-0.306', '-0.198', '-0.0852', '-0.12115', '-1.002', '0.06052', '0.06836', '-0.2461', '0.0859', '0.2825', '0.2167', '-0.1384', '0.3867', '0.11993', '0.0846', '0.4656', '-0.1366', '-0.292', '-0.8926', '0.2837', '0.4724', '0.0492', '0.3762', '0.4263', '0.1239', '0.857', '0.3513', '-0.3228', '-0.2126', '0.703', '0.2325', '-1.178', '-0.402', '0.07837', '0.1556', '0.571', '0.4', '-0.10754', '0.3516', '0.1066', '0.1089', '-0.1238', '0.293', '0.2019', '0.066', '-0.00782', '-0.315', '0.4739', '0.4136', '0.2683', '-0.1619', '0.593', '-0.3667', '0.2172', '0.5503', '0.1646', '0.6313', '0.2678', '1.015', '0.2957', '-0.392', '0.2688', '0.1103']",,,C563463,,,,
mondo:0012137,Carney complex - trismus - pseudocamptodactyly syndrome,"['Carney complex variant', 'CARNEY complex variant']",,608837,319340,,"['-0.2832', '-0.02672', '0.3403', '-0.11926', '0.01985', '-0.252', '0.01764', '0.1819', '-0.498', '-0.07166', '-0.0874', '0.0767', '-0.1545', '0.1941', '-0.02635', '0.2634', '0.1501', '-0.0384', '0.3286', '-0.4922', '-0.00471', '0.00454', '0.1786', '0.1318', '-0.1423', '0.61', '0.014046', '0.1211', '0.1493', '-0.04926', '0.1317', '-0.1449', '0.2101', '0.292', '0.0809', '-0.3296', '0.02129', '-0.0523', '-0.1722', '-0.2428', '0.0749', '-0.4639', '-0.0338', '0.0293', '0.1459', '-0.3684', '-0.269', '0.5693', '-0.05038', '0.03357', '-0.3367', '0.0061', '0.10956', '0.02733', '-0.527', '-0.3733', '0.311', '-0.2307', '-0.2233', '-0.224', '0.1875', '-0.0011635', '-0.1823', '-0.03061', '-0.2693', '-0.01042', '0.2708', '0.3684', '-0.1724', '0.01061', '-0.456', '-0.1852', '0.095', '0.244', '0.2324', '0.0494', '-0.1276', '0.1134', '-0.2018', '-0.3796', '0.1295', '-0.01617', '0.2449', '0.352', '0.0934', '-0.03714', '0.1719', '0.3787', '0.1917', '-0.002151', '0.254', '0.1355', '0.309', '-0.001002', '0.38', '-0.10394', '0.427', '-0.2942', '0.0578', '0.5435']",,,,,,,
mondo:0012138,muscular dystrophy-dystroglycanopathy type B6,"['muscular dystrophy-dystroglycanopathy (congenital with mental retardation), type B, 6', 'congenital muscular dystrophy type 1D', 'muscular dystrophy, congenital, large-related', 'congenital muscular dystrophy large-related', 'muscular dystrophy, congenital, type 1D', 'MDC1D', 'muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B, 6', 'MDDGB6']",0110637,608840,98894,C1837229,"['-0.2388', '-0.5454', '-0.4683', '-0.3936', '0.819', '-1.174', '0.131', '0.4575', '-1.79', '-0.6294', '-0.00196', '0.3909', '-0.1139', '0.7812', '0.2162', '0.2299', '-0.753', '-0.4565', '-0.5034', '-0.8433', '-0.05585', '0.2477', '0.4065', '0.582', '0.2097', '-0.0901', '0.10333', '-0.8813', '0.2554', '-0.3435', '0.735', '0.0665', '0.791', '0.2014', '0.3325', '-0.1688', '-0.511', '0.3713', '0.2324', '-0.553', '0.2656', '-0.2474', '-0.601', '0.3042', '-0.335', '0.3003', '0.2499', '0.6953', '-0.001584', '0.4675', '0.3325', '-0.3518', '0.2063', '-0.7275', '0.10345', '-0.295', '0.393', '0.744', '-0.3433', '0.2323', '0.1353', '-0.0005956', '-0.04468', '0.1936', '-0.0654', '0.0232', '0.03897', '0.716', '-0.3022', '-0.2832', '-0.0995', '0.603', '-0.09985', '-0.2094', '0.7515', '0.4995', '0.1254', '0.519', '0.294', '0.1914', '0.2856', '0.0892', '-0.332', '0.38', '-0.2637', '-0.1824', '-0.1823', '-0.315', '1.038', '0.2695', '-0.2935', '0.11194', '0.4111', '0.745', '-0.5063', '0.1581', '0.2668', '-0.3684', '-0.3804', '-0.0954']",,,C563844,,,,
mondo:0012139,"macular dystrophy, retinal, 3","['MCDR3', 'macular dystrophy, retinal, 3', 'macular dystrophy, retinal, type 3', 'Mcdr3']",,608850,,C3888009,,,,,,,,
mondo:0012141,"orofacial cleft 6, susceptibility to","['IRF6 orofacial cleft', 'orofacial cleft 6, susceptibility to', 'susceptibility to orofacial cleft 6', 'orofacial cleft caused by mutation in IRF6', 'OFC6', 'cleft lip with or without cleft palate, nonsyndromic, 6', 'orofacial cleft 6']",0080593,608864,,,"['-0.01988', '0.04776', '0.01689', '-0.0361', '0.0474', '-0.06525', '0.006535', '0.065', '-0.05267', '-0.0513', '-0.01857', '0.01926', '0.006187', '0.007553', '-0.02908', '-0.02176', '0.005016', '-0.05072', '-0.023', '-0.1103', '0.01348', '-0.00935', '0.0737', '-0.00827', '-0.007572', '0.002926', '-0.0181', '-0.002785', '0.00196', '-0.0327', '0.05603', '-0.004723', '0.06232', '0.012886', '0.00844', '-0.03882', '-0.01194', '-0.03564', '-0.0293', '-0.05695', '0.04144', '-0.05524', '0.02867', '-0.0321', '-0.015434', '-0.0522', '-0.01518', '0.0454', '-0.012245', '0.02014', '-0.0461', '-0.03946', '0.00845', '-0.005623', '-0.03177', '-0.01898', '0.04898', '-0.03613', '-0.06616', '0.01773', '0.05145', '0.0201', '-0.02571', '0.01855', '-0.007664', '0.00405', '0.0737', '0.05832', '-0.0654', '0.07306', '-0.05554', '-0.01352', '0.007545', '-0.04953', '0.02277', '0.02939', '0.0003598', '-0.01826', '-0.0472', '-0.02942', '0.003633', '-0.01172', '0.001913', '0.0815', '-0.02289', '0.0255', '0.013275', '0.0673', '0.06683', '0.003786', '0.005096', '0.05676', '-0.013855', '0.01898', '0.1447', '0.01898', '0.0573', '-0.072', '-0.0008264', '0.02235']",,,,,,,
mondo:0012142,orofacial cleft 5,"['cleft lip with or without cleft palate, nonsyndromic, 5', 'orofacial cleft type 5', 'orofacial cleft caused by mutation in MSX1', 'MSX1 orofacial cleft', 'orofacial cleft 5', 'OFC5']",0080399,608874,,C1837210,,,,C563843,,,,
mondo:0012143,hereditary cryohydrocytosis with reduced stomatin,"['ChC type 2', 'SDCHCN', 'cryohydrocytosis, stomatin-deficient, with mental retardation, seizures, cataracts, and massive hepatosplenomegaly', 'stomatin-deficient cryohydrocytosis', 'stomatin-deficient cryohydrocytosis with neurologic defects', 'sdCHC', 'hereditary cryohydrocytosis type 2', 'GLUT1 deficiency syndrome with pseudohyperkalemia and hemolysis', 'cryohydrocytosis, stomatin-deficient, with intellectual disability, seizures, cataracts, and massive hepatosplenomegaly']",,608885,168577,C1837206,"['-0.3638', '0.05823', '0.095', '-0.1256', '-0.0682', '-0.1523', '-0.3228', '0.342', '0.026', '0.01855', '-0.07935', '-0.01929', '0.0797', '-0.1901', '-0.1353', '-0.04477', '0.0971', '-0.1238', '0.013855', '-0.6333', '0.08813', '-0.1703', '0.3333', '0.1346', '0.2307', '0.05798', '0.01761', '-0.12384', '0.0653', '-0.1421', '-0.07214', '0.05615', '0.301', '0.4707', '-0.07837', '-0.1798', '-0.383', '-0.2773', '-0.2411', '-0.377', '-0.1398', '-0.3035', '0.1277', '-0.02026', '-0.1051', '-0.3645', '-0.06665', '0.03647', '0.1549', '0.0802', '-0.06824', '0.2289', '0.08563', '0.1595', '0.0905', '-0.093', '0.229', '-0.11993', '-0.298', '0.155', '0.0757', '-0.03326', '0.1863', '-0.0796', '-0.02946', '-0.1844', '0.4165', '0.552', '-0.1029', '0.26', '-0.1407', '-0.01884', '-0.1459', '-0.0673', '0.0958', '-0.11505', '0.378', '-0.1296', '-0.003695', '-0.03705', '0.0732', '-0.1677', '0.02248', '0.253', '0.1032', '-0.1179', '-0.002972', '0.2039', '0.3552', '-0.1724', '0.4937', '0.1786', '0.2358', '-0.135', '0.2825', '0.4204', '0.1981', '-0.0385', '0.1255', '0.2073']",,,C563840,,,,
mondo:0012144,Waardenburg syndrome type 2D,"['SNAI2 Waardenburg syndrome type 2', 'Waardenburg syndrome type 2 caused by mutation in SNAI2', 'Waardenburg syndrome type IID', 'WS2D', 'Waardenburg syndrome, type 2D']",0110952,608890,,C1837203,,,,C563839,,,,
mondo:0012145,"macular degeneration, age-related, 3","['FBLN5 age-related macular degeneration', 'neuropathy, hereditary, with or without age-related macular degeneration', 'ARMD3', 'macular degeneration, age-related, 3', 'neuropathy, hereditary, with or without age-related macular Degeneration', 'macular Degeneration, age-related, type 3', 'age-related macular degeneration caused by mutation in FBLN5', 'HNARMD']",,608895,,C1837187,,,,C563838,,,,
mondo:0012146,familial hemophagocytic lymphohistiocytosis 3,"['hemophagocytic lymphohistiocytosis, familial, type 3', 'HLH3', 'Hlh3', 'familial hemophagocytic lymphohistiocytosis type 3', 'genetic hemophagocytic lymphohistiocytosis caused by mutation in UNC13D', 'FHL3', 'UNC13D genetic hemophagocytic lymphohistiocytosis', 'Hplh3', 'hemophagocytic lymphohistiocytosis, familial, 3', 'HPLH3']",0110923,608898,540,,"['-0.00881', '0.1256', '0.02121', '-0.1667', '-0.128', '-0.2722', '0.02168', '0.1206', '-0.0815', '0.0357', '-0.05347', '-0.0736', '-0.2102', '-0.003504', '-0.0814', '-0.11145', '-0.1096', '-0.0339', '0.04504', '-0.4211', '-0.0612', '-0.2167', '0.3406', '0.0223', '-0.00846', '0.02322', '-0.10706', '-0.2141', '-0.02867', '-0.252', '0.1985', '0.08856', '0.371', '0.10114', '0.0765', '-0.04312', '-0.2522', '-0.11365', '-0.208', '-0.2086', '0.05276', '-0.3435', '0.03442', '-0.10925', '-0.1482', '0.0752', '-0.1641', '0.0309', '0.0604', '0.06995', '0.0442', '-0.01859', '0.1309', '-0.0636', '-0.1785', '-0.092', '0.0637', '-0.1754', '-0.1498', '0.1741', '0.2827', '0.1921', '0.00997', '-0.04175', '0.2064', '-0.1088', '0.2212', '0.07446', '-0.1447', '0.324', '-0.1416', '-0.11835', '-0.001451', '-0.004147', '-0.0091', '-0.06067', '-0.10626', '0.09265', '-0.07043', '-0.1009', '-0.1135', '0.007282', '-0.1454', '0.1166', '-0.2086', '-0.06506', '0.1301', '0.0303', '0.2788', '0.02184', '0.2487', '0.0373', '0.03552', '0.007607', '0.4172', '0.1947', '0.2795', '-0.2236', '-0.05142', '0.01153']",,,C537251,,,,
mondo:0012147,"coronary heart disease, susceptibility to, 5","['coronary heart disease, susceptibility to, 5', 'KALRN coronary artery disease', 'coronary artery disease caused by mutation in KALRN', 'coronary artery disease, early-onset', 'coronary heart disease, susceptibility to, type 5', 'susceptibility to coronary heart disease 5', 'Chds5']",,608901,,,,,,,,,,
mondo:0012149,"attention deficit-hyperactivity disorder, susceptibility to, 1","['ADHD1', 'attention deficit-hyperactivity disorder, susceptibility to, type 1', 'attention deficit-hyperactivity disorder, susceptibility to, 1']",,608903,,,,,,,,,,
mondo:0012150,"attention deficit-hyperactivity disorder, susceptibility to, 2","['ADHD2', 'attention deficit-hyperactivity disorder, susceptibility to, 2', 'attention Deficit-hyperactivity disorder, susceptibility to, type 2']",,608904,,,,,,,,,,
mondo:0012151,"attention deficit-hyperactivity disorder, susceptibility to, 3","['attention Deficit-hyperactivity disorder, susceptibility to, type 3', 'ADHD3', 'attention deficit-hyperactivity disorder, susceptibility to, 3']",,608905,,,,,,,,,,
mondo:0012152,"attention deficit-hyperactivity disorder, susceptibility to, 4","['attention Deficit-hyperactivity disorder, susceptibility to, type 4', 'ADHD4', 'attention deficit-hyperactivity disorder, susceptibility to, 4']",,608906,,,,,,,,,,
mondo:0012153,Alzheimer disease 9,"['AD9', 'Alzheimer disease 9, susceptibility to', 'Alzheimer disease 9', 'Alzheimer disease 9, late-onset']",0111364,608907,,C1837149,,,,C563834,,,,
mondo:0012154,myopia 6,"['myopia type 6', 'MYP6', 'SCO2 myopia (disease)', 'myopia 6', 'myopia, susceptibility to']",,608908,,,,,,C536105,,,,
mondo:0012155,choanal atresia,"['choanal atresia, POSTERIOR', 'posterior choanal atresia', 'atresia of nares', 'PCA', 'imperforate nares']",9574,608911,137914,,,,,D002754,748.0,Q30.0,10008587,
mondo:0012156,"myasthenic syndrome, congenital, 1B, fast-channel","['myasthenic syndrome, congenital, 1B, FAST-channel', 'congenital myasthenic syndrome type 1B', 'congenital myasthenic syndrome 1B, fast-channel', 'congenital myasthenic syndrome 1B', 'myasthenic syndrome, congenital, 1B, fast-channel', 'CMS1B']",0110662,608930,,C4225405,,,,,,,,
mondo:0012157,congenital myasthenic syndrome 4C,"['FIM1', 'congenital myasthenic syndrome 4C associated with acetylcholine receptor deficiency', 'myasthenic syndrome, congenital, type Id', 'CMS Id', 'Cms Id', 'myasthenia, familial infantile, 1', 'myasthenia, familial infantile, 1, formerly', 'congenital myasthenic syndrome associated with acetylcholine receptor deficiency', 'CMS1D', 'CMS4C', 'familial infantile myasthenia 1', 'myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency', 'congenital myasthenic syndrome type 4C', 'Cms Id, formerly', 'myasthenic syndrome, congenital, 4C, associated with acetylcholine receptor deficiency', 'congenital myasthenic syndrome type Id']",0110679,608931,,,,,,,,,,
mondo:0012158,keratoconus 2,"['KTCN2', 'keratoconus 2']",,608932,,C1837090,,,,C563827,,,,
mondo:0012159,lung cancer susceptibility 1,"['lung cancer susceptibility', 'LNCR1', 'lung cancer susceptibility 1']",,608935,,C1837089,,,,,,,,
mondo:0012160,spondylometaphyseal dysplasia-cone-rod dystrophy syndrome,"['SMDCRD', 'SmD-CRD', 'spondylometaphyseal dysplasia with cone-rod dystrophy']",0112300,608940,85167,C1837073,"['-0.5464', '0.1278', '0.2234', '-0.2417', '0.498', '-0.6167', '-0.04544', '0.595', '-0.2983', '-0.494', '-0.237', '-0.05295', '-0.1659', '-0.1274', '0.2471', '-0.02449', '0.487', '0.0452', '-0.3638', '-0.3933', '-0.05618', '0.00976', '0.1033', '-0.0094', '0.08167', '0.1334', '-0.2302', '-0.4058', '0.02109', '-0.067', '0.0859', '0.01135', '-0.05948', '0.129', '0.2018', '-0.1927', '0.05774', '-0.334', '0.1289', '-0.1149', '0.04694', '-0.4429', '-0.1815', '-0.16', '-0.1915', '-0.1368', '-0.06976', '0.0781', '-0.07947', '-0.4175', '0.2808', '-0.02838', '0.2986', '0.1205', '-0.02744', '-0.3755', '0.3127', '-0.0427', '-0.4905', '0.1445', '0.3025', '0.04245', '-0.1829', '-0.05807', '0.0886', '-0.3608', '0.1334', '0.5576', '-0.358', '-0.011444', '-0.2866', '-0.2666', '0.1792', '-0.1232', '0.1973', '0.0821', '-0.1395', '0.05133', '-0.05533', '-0.03607', '0.25', '0.402', '-0.1421', '0.501', '-0.2595', '0.1586', '0.07806', '0.335', '0.1407', '0.1663', '0.09656', '0.1262', '0.1029', '0.1611', '0.5195', '0.049', '0.5483', '-0.5195', '0.2725', '0.08636']",,,C563825,,,,
mondo:0012161,susceptibility to respiratory infections associated with CD8alpha chain mutation,"['CD8 deficiency, familial', 'familial CD8 deficiency']",,608957,169085,C1837065,"['-0.5693', '0.1976', '-0.04865', '-0.1982', '0.00222', '-0.3882', '0.6084', '-0.10864', '-0.10504', '0.2747', '-0.10144', '0.01653', '-0.1815', '0.123', '0.3389', '0.0778', '-0.3', '0.1981', '-0.1202', '-0.553', '0.0592', '0.03427', '1.004', '0.2705', '0.09265', '-0.11053', '-0.1921', '0.363', '-0.1417', '-0.3213', '0.487', '0.626', '0.5044', '0.0557', '-0.1537', '-0.3027', '-0.241', '0.1482', '-0.2527', '-0.5483', '-0.09973', '0.00211', '-0.1208', '-0.2695', '-0.6304', '-0.489', '-0.4438', '-0.3772', '0.2952', '0.2964', '-0.0736', '-0.3228', '0.4854', '0.05646', '-0.03223', '-0.0981', '0.1807', '-0.5654', '0.1301', '0.422', '-0.3022', '0.6484', '0.05304', '0.0699', '0.113', '0.10394', '0.288', '0.5596', '-0.5366', '0.1455', '-0.1357', '-0.10614', '-0.081', '-0.03653', '0.2883', '-0.3892', '0.6455', '-0.01247', '0.2224', '-0.0361', '-0.5825', '-0.05978', '-0.0629', '0.1958', '-0.3735', '-0.08044', '0.1566', '0.1981', '0.551', '0.02316', '0.326', '0.3591', '-0.3767', '-0.214', '0.773', '0.809', '0.255', '-0.511', '-0.3992', '0.0966']",,,C563824,,,,
mondo:0012162,patterned macular dystrophy 2,"['CTNNA1 patterned macular dystrophy', 'butterfly-shaped pigmentary maculary dystrophy 2', 'patterned macular dystrophy caused by mutation in CTNNA1', 'MDPT2', 'macular dystrophy, patterned, type 2', 'macular dystrophy, patterned, 2', 'patterned macular dystrophy type 2', 'macular dystrophy, butterfly-Shaped pigmentary, 2']",0060864,608970,,C1837029,,,,,,,,
mondo:0012163,immunodeficiency 104,"['severe combined immunodeficiency, T cell-negative, B-cell/natural killer-cell positive', 'severe combined immunodeficiency, T-cell negative, B-cell/natural killer cell-positive type', 'autosomal recessive T cell-negative, B-cell positive, NK cell-positive SCID', 'SCID, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive', 'autosomal recessive T cell-negative, B-cell negative, NK cell-positive SCID', 'severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, NK cell-positive', 'IMD104']",0090014,608971,169160,C1837028,"['-0.1449', '0.1214', '0.0924', '-0.04916', '0.0692', '-0.0854', '0.0879', '0.09235', '-0.0774', '-0.0938', '-0.02838', '-0.0347', '-0.05005', '0.03026', '-0.02567', '-0.1187', '0.013916', '-0.03516', '-0.12396', '-0.2188', '-0.0756', '-0.087', '0.1715', '-0.04575', '0.011345', '0.002615', '0.00565', '-0.02943', '-0.04123', '-0.1287', '0.0735', '0.1156', '0.202', '0.0556', '0.0079', '-0.0937', '-0.08734', '-0.05988', '-0.06174', '-0.1525', '0.03418', '-0.1436', '0.009514', '-0.05374', '-0.12305', '-0.09564', '-0.04608', '0.01965', '0.0456', '0.06247', '0.02406', '-0.12067', '0.1074', '0.01767', '-0.1597', '0.03394', '0.0838', '-0.12213', '-0.1292', '0.05035', '0.04398', '0.0856', '-0.00706', '0.0434', '0.1082', '0.005146', '0.1002', '0.09033', '-0.1301', '0.1233', '-0.0897', '0.01282', '0.02982', '-0.1053', '0.09247', '0.0727', '0.10046', '-0.02332', '0.0003467', '0.01462', '-0.04077', '-0.02234', '-0.06134', '0.1053', '-0.009415', '0.006683', '0.12177', '0.11707', '0.2297', '-0.0007935', '0.0733', '0.1186', '-0.0873', '0.01614', '0.2842', '0.1582', '0.0857', '-0.2488', '-0.03156', '0.05112']",,,C563822,,,,
mondo:0001302,hypertensive heart disease,,11516,,,C0152105,,C4907,,,402.9,,,
mondo:0001303,abnormal pupillary function,"['abnormal pupillary function', 'abnormal pupillary function (disease)']",11518,,,,,,,,379.49,,,0007686
mondo:0001304,benign hypertensive renal disease,"['hypertensive renal disease, benign', 'hypertensive renal disease, benign, without mention of renal failure']",11520,,,C0155596,,,,,403.10,,,
mondo:0001305,laryngostenosis,['stenosis of larynx'],11527,,,C0023075,,,,D007829,478.74,J38.6,,0001602
mondo:0001307,corneal abscess,,11543,,,C0155091,,C26969,,,370.55,,,
mondo:0001308,corneal deposit,['deposits - cornea'],11547,,,C0162281,,,,,371.10,H18.0,,
mondo:0001309,oculomotor nerve paralysis,"['oculomotor nerve cranial nerve palsy', 'oculomotor palsy', 'III nerve palsy', 'third cranial nerve paralysis', 'cranial nerve palsy of oculomotor nerve', 'IIIrd nerve paralysis']",11550,,98685,C0028866,,C27597,,,,,,
mondo:0001310,Bowman^s membrane folds or rupture,['Bowman membrane folds or rupture'],11552,,,C0155115,,,,,371.31,,,
mondo:0001312,acute serous otitis media,['acute non-suppurative otitis media - serous'],11557,,,C0155415,,,,,381.01,H65.0,,
mondo:0001313,acute allergic serous otitis media,,11558,,,C0155418,,,,,381.04,,,
mondo:0001314,chondrocalcinosis,"['pseudogout', 'calcium pyrophosphate deposition disease']",1156,,,,,C34955,,D002805,712.1,,,0000934
mondo:0001315,neurocirculatory asthenia,"['cardiovascular neurosis', 'Krishaber^s disease', 'cardiovascular malfunction arising from mental factors', 'Da Costa^s syndrome']",11569,,,,,,,D009449,306.2,,,
mondo:0001316,streptococcal meningitis,['Streptococcus caused infectious meningitis'],11574,,,C0154639,,,,,320.2,G00.2,,
mondo:0001317,phlyctenulosis,"['Phlyctenular keratoconjunctivitis', 'strumous ophthalmia']",11581,,,C0155080,,,,,370.31,,,
mondo:0001318,functional gastric disease,,1159,,,,,,,,536.9,,,
mondo:0001319,bladder lateral wall cancer,['malignant neoplasm of lateral wall of urinary bladder'],11593,,,C0496828,,,,,188.2,,,
mondo:0001320,ring staphyloma,,11594,,,C0155363,,,,,379.15,,,
mondo:0001322,pericardium cancer,"['malignant tumour of the pericardium', 'malignant tumor of pericardium', 'malignant pericardial tumour', 'pericardial tumour', 'malignant neoplasm of pericardium', 'pericardium cancer', 'pericardial tumor', 'malignant neoplasm of the pericardium', 'malignant pericardial tumor', 'malignant tumour of pericardium', 'cancer of pericardium', 'malignant tumor of the pericardium', 'malignant pericardium neoplasm', 'malignant pericardial neoplasm']",116,,,C0346609,,C4567,,,,,,
mondo:0001323,infant gynecomastia,"['breast engorgement in newborn', 'neonatal gynaecomastia']",11603,,,C1449721,,,,,778.7,P83.4,,
mondo:0001325,penile cancer,"['malignant tumour of the penis', 'malignant penile neoplasm', 'malignant neoplasm of body of penis', 'malignant neoplasm of the penis', 'penile neoplasm', 'malignant penile tumor', 'malignant penile tumour', 'malignant tumor of the penis', 'malignant tumor of penis', 'penile Ca', 'penis cancer', 'malignant neoplasm of penis', 'Ca penis', 'malignant tumour of penis', 'malignant penis neoplasm', 'cancer of penis', 'penile cancer']",11615,,398043,CN226091,,C7547,,,187.4,,,
mondo:0001326,dental pulp necrosis,"['necrotic pulp', 'necrosis of the pulp', 'pulp necrosis']",11623,,,C0011407,,,,D003790,522.1,K04.1,,
mondo:0001327,pelvic muscle wasting,,11629,,,,,,,,618.83,N81.84,,
mondo:0001328,thyroid hormone resistance syndrome,"['generalised thyroid hormone resistance', 'RTH', 'thyroid hormone responsiveness defect', 'generalized thyroid hormone resistance', 'thyroid hormone resistance']",11633,,,CN118820,,,,D018382,259.8,,,
mondo:0001329,accommodative spasm,['spasm of accommodation'],11637,,,C0152196,,,,,367.53,,,
mondo:0001330,presbyopia,,11638,,,C0033075,,,,D011305,367.4,H52.4,,
mondo:0001331,conjunctival deposit,,11653,,,C0162280,,,,,372.56,,,
mondo:0001332,palindromic rheumatism,"['Hench^s syndrome', 'Hench-Rosenberg syndrome']",1166,,,C0085574,,,,C538103,719.38,M12.3,,
mondo:0001334,hypertrichosis of eyelid,['eyelid hypertrichosis (disease)'],11669,,,C0155213,,,,,374.54,,,
mondo:0001335,hypotrichosis of eyelid,['eyelid hypotrichosis'],11671,,,C0155214,,,,,374.55,,,
mondo:0001336,familial hyperlipidemia,"['hyperlipidaemia', 'familial hyperlipoproteinemia', 'hyperlipemia', 'hereditary hyperlipidemia (disease)']",1168,,,C0020476,,C34709,,D006949,,E78.5,,
mondo:0001337,inflamed seborrheic keratosis,,11685,,,C0376117,,,,,702.11,L82.0,,
mondo:0001338,acute apical periodontitis,['acute apical periodontitis of pulpal origin'],11693,,,C4084770,,,,,522.4,K04.4,,
mondo:0001339,portal vein thrombosis,"['portal vein thrombotic disease', 'thrombotic disease of portal vein']",11695,,,C0155773,,C78565,,,452,I81,,
mondo:0001340,heart cancer,"['malignant neoplasm of heart', 'malignant heart tumour', 'malignant heart neoplasm', 'malignant Cardiac neoplasm', 'malignant Cardiac tumour', 'malignant tumor of heart', 'malignant tumour of the heart', 'malignant tumour of heart', 'malignant Cardiac tumor', 'malignant tumor of the heart', 'tumor of heart', 'tumour of heart', 'cancer of heart', 'Cardiac tumor', 'heart cancer', 'Cardiac tumour', 'Cardiac neoplasm, malignant', 'malignant neoplasm of the heart', 'malignant heart tumor']",117,,,,,C3548,,D006338,164.1,,,
mondo:0006385,primary intraosseous squamous cell carcinoma,['PIOSCC'],,,,C1709663,,C54295,1000492,,,,,
mondo:0006386,primary peritoneal serous adenocarcinoma,['primary peritoneal serous adenocarcinoma'],,,,C1514429,,C40023,1000494,,,,,
mondo:0006387,primary pulmonary diffuse large B-cell lymphoma,"['lung diffuse large B-cell lymphoma', 'pulmonary diffuse large B-cell lymphoma', 'high grade MALT lymphoma of the lung', 'primary pulmonary diffuse large B-cell lymphoma']",,,,C1709666,,C45605,1000495,,,,,
mondo:0006388,prolactin-producing pituitary gland carcinoma,"['malignant prolactin secreting pituitary gland tumor', 'malignant prolactin producing tumour of the pituitary gland', 'malignant prolactin producing neoplasm of the pituitary', 'malignant prolactin producing tumour of the pituitary', 'malignant prolactin secreting tumour of pituitary gland', 'malignant prolactin secreting neoplasm of pituitary gland', 'malignant prolactin secreting pituitary gland tumour', 'malignant prolactin secreting tumour of the pituitary', 'malignant prolactin secreting tumour of pituitary', 'malignant prolactinoma of pituitary gland', 'malignant prolactinoma of the pituitary', 'malignant prolactin producing tumor of pituitary gland', 'malignant prolactin secreting neoplasm of pituitary', 'prolactin-producing pituitary gland carcinoma', 'malignant prolactin producing pituitary gland neoplasm', 'malignant prolactin producing tumour of pituitary', 'PRL producing pituitary gland carcinoma', 'malignant prolactin secreting pituitary tumor', 'malignant prolactin secreting pituitary neoplasm', 'malignant prolactin producing tumour of pituitary gland', 'malignant pituitary prolactinoma', 'malignant prolactin secreting pituitary tumour', 'malignant prolactinoma', 'malignant prolactin producing pituitary gland tumour', 'malignant prolactin producing tumor of the pituitary', 'malignant prolactin producing tumour', 'malignant prolactin producing tumor', 'malignant prolactin secreting tumor of pituitary gland', 'malignant prolactinoma of pituitary', 'malignant prolactin secreting tumor of the pituitary', 'malignant prolactin secreting tumor of the pituitary gland', 'malignant prolactin producing neoplasm of pituitary', 'malignant prolactin producing pituitary neoplasm', 'prolactin producing pituitary gland carcinoma', 'malignant prolactin producing neoplasm of pituitary gland', 'malignant prolactin producing pituitary tumour', 'malignant prolactin producing neoplasm of the pituitary gland', 'malignant prolactin secreting tumour of the pituitary gland', 'malignant pituitary gland prolactinoma', 'malignant prolactinoma of the pituitary gland', 'malignant prolactin secreting neoplasm of the pituitary', 'malignant prolactin secreting neoplasm of the pituitary gland', 'malignant prolactin producing pituitary gland tumor', 'malignant prolactin producing tumor of the pituitary gland', 'malignant prolactin producing pituitary tumor', 'malignant prolactin producing tumor of pituitary', 'malignant prolactin secreting tumor of pituitary', 'malignant prolactin secreting pituitary gland neoplasm']",,,,C1334614,,C5962,1000497,,,,,
mondo:0006389,prostate rhabdomyosarcoma,"['rhabdomyosarcoma of prostate', 'prostate rhabdomyosarcoma', 'prostate gland rhabdomyosarcoma (disease)', 'rhabdomyosarcoma of the prostate']",3252,,,C1335518,,C5522,1000498,,,,,
mondo:0006390,prostate small cell carcinoma,"['prostate small cell neuroendocrine carcinoma', 'Oat cell carcinoma of prostate', 'small cell carcinoma of prostate', 'small cell carcinoma of prostate gland', 'PRSCC', 'prostate oat cell carcinoma', 'prostate small cell NEC', 'prostate small cell carcinoma', 'prostate gland small cell carcinoma', 'small cell carcinoma of the prostate', 'Oat cell carcinoma of the prostate', 'prostate Oat cell carcinoma']",7141,,,C1300585,,C6766,1000499,,,,,
mondo:0006391,pyloric gland adenoma,"['pyloric gland adenoma', 'pyloric gastric gland adenoma']",,,,C1709780,,C43526,1000501,,,,,
mondo:0006392,rectal hyperplastic polyp,"['hyperplastic polyp of rectum', 'rectal metaplastic polyp', 'rectal Hp', 'rectal MP', 'hyperplastic polyp of the rectum']",,,,C1335679,,C5619,1000502,,,,,
mondo:0006393,rectal traditional serrated adenoma,"['rectal traditional serrated adenoma', 'rectal serrated adenoma', 'rectal serrated adenoma type II', 'rectal TSA']",,,,C3272790,,C96463,1000503,,,,,
mondo:0006394,rectal tubular adenoma,['rectal tubular adenoma'],,,,C3272804,,C96477,1000504,,,,,
mondo:0006395,rectal tubulovillous adenoma,"['rectal tubulovillous adenoma', 'rectal Villotubular adenoma', 'Villotubular adenoma of the rectum', 'Villotubular adenoma of rectum', 'tubulovillous adenoma of the rectum', 'tubulovillous adenoma of rectum']",,,,C1335691,,C5620,1000505,,,,,
mondo:0006396,rectal villous adenoma,"['rectal villous adenoma', 'rectum villous adenoma', 'villous adenoma of rectum', 'villous adenoma of the rectum']",,,,C0730199,,C4919,1000506,,,,,
mondo:0006397,renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions,"['translocation-associated renal cell carcinoma', 'tRCC', 'Xp11.2 translocation-related renal cell carcinoma', 'renal cell cancer associated with Xp11.2 translocations/TFE3 Gene fusions', 'TFE3-Rearranged renal cell carcinoma', 'renal cell carcinoma associated with Xp11.2 translocations/TFE3 gene fusions']",,,,C1337036,,C27891,1000508,,,,,
mondo:0006398,retroperitoneal inflammatory myofibroblastic tumor,"['retroperitoneal space inflammatory myofibroblastic tumour', 'retroperitoneal space inflammatory myofibroblastic tumor', 'retroperitoneal inflammatory myofibroblastic tumor']",,,,C1514921,,C39741,1000510,,,,,
mondo:0006400,salivary gland acinic cell carcinoma,"['acinic cell tumor of salivary gland', 'salivary gland acinic cell tumor', 'acinic cell carcinoma of salivary gland', 'acinic cell tumor of the salivary gland', 'salivary gland acinic cell cancer', 'salivary gland acinic cell tumour', 'salivary gland acinic cell neoplasm', 'acinic cell tumour of the salivary gland', 'acinic cell neoplasm of the salivary gland', 'acinic cell carcinoma of the salivary gland', 'acinic cell neoplasm of salivary gland', 'acinic cell tumour of salivary gland']",,,,C0279738,,C8013,1000513,,,,,
mondo:0006401,salivary gland adenosquamous carcinoma,"['saliva-secreting gland adenosquamous carcinoma', 'salivary gland adenosquamous carcinoma']",,,,C1335894,,C35737,1000514,,,,,
mondo:0006402,salivary gland basal cell adenocarcinoma,"['skin basal cell carcinoma of saliva-secreting gland', 'saliva-secreting gland skin basal cell carcinoma', 'basal cell adenocarcinoma of the salivary gland', 'salivary gland basal cell adenocarcinoma', 'basal cell adenocarcinoma', 'basal cell adenocarcinoma of salivary gland']",,,,,,C3678,1000515,,,,,
mondo:0006403,salivary gland carcinoma ex pleomorphic adenoma,"['salivary gland carcinoma ex pleomorphic adenoma', 'saliva-secreting gland carcinoma ex pleomorphic adenoma', 'pleomorphic adenoma carcinoma']",297,,,C1519172,,C40410,1000516,,,,,
mondo:0006404,salivary gland large cell carcinoma,"['saliva-secreting gland large cell carcinoma', 'large cell undifferentiated salivary gland carcinoma', 'large cell salivary gland carcinoma', 'salivary gland large cell carcinoma']",,,,C2111671,,C35735,1000517,,,,,
mondo:0006405,salivary gland small cell carcinoma,"['neuroendocrine carcinoma of the salivary gland', 'neuroendocrine carcinoma of salivary gland', 'salivary gland neuroendocrine carcinoma', 'salivary gland anaplastic small cell carcinoma', 'salivary gland small cell carcinoma', 'small cell salivary gland carcinoma', 'anaplastic small cell carcinoma of the salivary gland', 'saliva-secreting gland small cell carcinoma', 'small cell carcinoma of saliva-secreting gland', 'anaplastic small cell carcinoma of salivary gland']",,,,C1335982,,C35703,1000519,,,,,
mondo:0006406,sarcomatoid carcinoma,"['spindle cell carcinoma', 'carcinoma, spindle cell, malignant', 'pseudosarcomatous carcinoma', 'spindle cell carcinoma (morphologic abnormality)', 'sarcomatoid carcinoma']",4015,,,C0205697,,C27004,1000520,,,,,
mondo:0006407,sarcomatoid mesothelioma,"['sarcomatoid mesothelioma (morphologic abnormality)', 'malignant fibrous mesothelioma', 'malignant fibrous mesothelioma (morphologic abnormality)', 'sarcomatoid mesothelioma', 'spindled mesothelioma']",4488,,,C0334513,,C45655,1000521,,,,,
mondo:0006408,sex hormone-producing adrenal cortex adenoma,"['Sex hormone producing adrenal cortex adenoma', 'Sex hormone producing adrenal cortical adenoma']",,,,C1710067,,C48452,1000523,,,,,
mondo:0006409,signet ring cell gastric adenocarcinoma,"['signet Ring cell adenocarcinoma of stomach', 'gastric signet ring cell adenocarcinoma', 'signet ring cell carcinoma of the stomach', 'signet Ring cell stomach adenocarcinoma', 'gastric signet Ring cell adenocarcinoma', 'signet Ring cell adenocarcinoma of the stomach', 'signet ring cell gastric adenocarcinoma']",8025,,,C1335965,,C5250,1000524,,,,,
mondo:0006410,simple endometrial hyperplasia,,,,,C0456483,,C35463,1000525,,621.31,,,
mondo:0006411,sinonasal undifferentiated carcinoma,"['Sinonasal anaplastic carcinoma', 'highly aggressive undifferentiated carcinoma of the nasal cavity and paranasal sinuses', 'undifferentiated Sinonasal cancer', 'sinonasal undifferentiated carcinoma', 'SNUC']",0080799,,,C1710096,,C54294,1000527,C537344,,,,
mondo:0000001,disease,"['disease or disorder', 'condition', 'diseases and disorders', 'disease', 'disorders', 'disorder', 'disease or disorder, non-neoplastic', 'diseases', 'other disease']",4,,377788,C0012634,,C2991,0000408,D004194,799.9,,,
mondo:0000004,adrenocortical insufficiency,"['adrenocortical insufficiency', 'corticoadrenal insufficiency', 'hypocortisolemia', 'hypoadrenalism', 'adrenal gland insufficiency', 'adrenal cortical hypofunction', 'hypocortisolism', 'adrenal insufficiency', 'adrenal cortical insufficiency']",10493,,,C0405580,,C26691,,D000309,255.41,,,
mondo:0000005,"alopecia, isolated",,,,,,,,,,,,,
mondo:0000009,"inherited bleeding disorder, platelet-type","['bleeding disorder, platelet-type', 'thrombocytopathy', 'platelet disorder', 'blood platelet disease']",2218,,,C0005818,,,,,,,,
mondo:0000014,"colorblindness, partial",,,,,,,,,,,,,
mondo:0000015,classic complement early component deficiency,['genetic deficiency of early component of the classical complement pathway'],,,,C1285186,,,,,279.8,,,
mondo:0000022,nocturnal enuresis,['sleep enuresis'],,,,,,C118172,,D053206,,,,
mondo:0000023,infantile liver failure,"['liver failure, infantile', 'infantile liver failure syndrome', 'fever-associated acute infantile liver failure syndrome']",0080716,,464724,CN228161,"['-0.02379', '0.05576', '0.02065', '-0.00848', '0.004864', '-0.0683', '0.0169', '0.07214', '-0.0527', '-0.03043', '-0.04187', '-0.02737', '-0.01657', '0.01657', '-0.0373', '-0.04047', '-0.01109', '-0.04562', '-0.03113', '-0.1025', '0.011215', '-0.04294', '0.04095', '-0.0295', '0.02011', '-0.04132', '-0.006126', '-0.00231', '-0.002287', '-0.0205', '0.04834', '0.007935', '0.06152', '0.01527', '0.02026', '-0.0119', '-0.03653', '-0.0308', '-0.01458', '-0.02641', '0.0006533', '-0.0504', '0.03195', '-0.002275', '-0.02063', '-0.03955', '-0.02745', '0.03568', '-0.02328', '0.03598', '-0.0294', '0.011185', '0.01299', '0.005817', '-0.03284', '-0.03455', '0.04016', '-0.01524', '-0.0682', '0.005985', '0.02748', '0.01727', '-0.007183', '-0.005684', '-0.006046', '-0.02046', '0.0773', '0.0612', '-0.0699', '0.0436', '-0.03084', '0.018', '0.015526', '-0.0421', '0.00872', '0.03027', '0.02834', '-0.0177', '-0.0313', '-0.004803', '-0.006214', '0.002748', '-0.04523', '0.01595', '0.00918', '0.00622', '0.02687', '0.03677', '0.0803', '0.0271', '0.03906', '0.02763', '-0.0123', '0.0195', '0.1096', '0.05066', '0.06494', '-0.07587', '0.001411', '0.005314']",,,,,,,
mondo:0000030,sleep-related hypermotor epilepsy,"['epilepsy, nocturnal frontal lobe', 'sleep-related hypermotor epilepsy']",,,,,,,,,,,,
mondo:0000032,"febrile seizures, familial","['seizures, familial febrile']",0111297,,,,,,,,,,,
mondo:0000044,hereditary hypophosphatemic rickets,['hereditary hypophosphatemic rickets'],,,437,,,,,,,E83.3,10060873,
mondo:0000045,"hypothyroidism, congenital, nongoitrous",,,,,,"['-0.01058', '0.01181', '0.00904', '-0.003164', '0.02184', '-0.02536', '0.00171', '0.01793', '-0.02834', '-0.02745', '-0.00839', '0.004578', '0.007057', '0.00955', '-0.00977', '-0.01826', '-0.007427', '-0.00895', '-0.01843', '-0.0478', '-0.000784', '-0.00541', '0.01743', '-0.00971', '0.002333', '-0.001049', '-0.000864', '-0.01034', '0.02043', '-0.0297', '0.01878', '0.001579', '0.0297', '0.0177', '0.001035', '-0.0005546', '-0.001798', '-0.00849', '0.003483', '-0.03314', '0.00978', '-0.01481', '0.01591', '-0.006527', '-0.003641', '-0.02475', '0.00841', '0.02083', '0.01005', '0.01188', '-0.01732', '0.01406', '0.006344', '-0.004757', '-0.017', '-0.003197', '0.02995', '-0.00774', '-0.02771', '0.00774', '0.01111', '0.01389', '-0.001749', '-0.004692', '0.003162', '-0.004314', '0.0165', '0.04416', '-0.03134', '0.02792', '-0.02472', '0.005554', '0.0001742', '-0.02287', '0.0181', '0.01437', '0.0165', '-0.00228', '-0.01569', '-0.007347', '-0.02087', '-0.004166', '-0.00821', '0.02484', '-0.00973', '0.00358', '0.02025', '0.00736', '0.04507', '-0.01279', '0.0215', '0.01909', '-0.00925', '0.009315', '0.04987', '0.00787', '0.0253', '-0.027', '0.000293', '0.01199']",,,,,,,
mondo:0000050,isolated congenital growth hormone deficiency,"['ICGHD', 'congenital isolated GH deficiency', 'congenital IGHD', 'isolated growth hormone deficiency', 'congenital isolated growth hormone deficiency', 'familial isolated growth hormone deficiency', 'non-acquired isolated growth hormone deficiency', 'IGHD']",0060870,,631,C0013338,"['-0.056', '0.05807', '0.0001756', '-0.007557', '0.03763', '-0.0367', '0.01888', '0.07404', '-0.05347', '-0.04413', '-0.009514', '0.006844', '0.01133', '0.02597', '-0.0331', '-0.035', '0.008675', '-0.01913', '-0.0522', '-0.1451', '-0.004536', '-0.0342', '0.05243', '-0.01906', '0.02188', '-0.01156', '-0.01492', '-0.0299', '0.01598', '-0.0495', '0.05896', '-0.002121', '0.05893', '0.034', '-0.001732', '-0.01813', '-0.01014', '-0.03354', '-0.01596', '-0.04178', '0.02867', '-0.0551', '0.03082', '-0.00986', '-0.00584', '-0.06335', '0.0139', '0.03378', '0.02158', '0.03235', '-0.02972', '-0.03293', '0.00998', '0.01692', '-0.04755', '-0.01107', '0.05438', '-0.03152', '-0.08453', '0.003096', '0.04083', '0.02336', '0.002728', '0.002304', '-0.002476', '0.007614', '0.07056', '0.0545', '-0.06793', '0.04846', '-0.05978', '0.03032', '0.014565', '-0.06085', '0.0316', '0.02771', '0.02332', '-0.02736', '-0.03806', '-0.02023', '-0.008575', '0.001907', '-0.02962', '0.04285', '-0.00495', '-0.003265', '0.0333', '0.02429', '0.1004', '0.02261', '0.0356', '0.06354', '-0.00449', '0.0081', '0.1362', '0.0359', '0.0568', '-0.094', '0.002815', '0.03146']",,,,,,10035083,
mondo:0000060,microcephalic osteodysplastic primordial dwarfism,,,,,CN239360,,,,,,,,
mondo:0000062,isolated microphthalmia,"['nonsyndromic microphthalmia', 'microphthalmia, isolated']",0080637,,,,,,,,,,,
mondo:0000065,"microvascular complications of diabetes, susceptibility",['microvascular complications of diabetes'],,,,CN357508,,,,,,,,
mondo:0000066,mitochondrial complex deficiency,,,,,,,,,,,,,
mondo:0000070,"mycobacterium tuberculosis, susceptibility",,,,,,,,,,,,,
mondo:0000075,"neuronopathy, distal hereditary motor",,,,,,,,,,,,,
mondo:0000078,acrocephalopolysyndactyly,['ACPS'],,,,C0687154,,,,,,,,
mondo:0000079,"nephrolithiasis/osteoporosis, hypophosphatemic",,0080655,,,,,,,,,,,
mondo:0000082,pelvic organ prolapse,,,,,C0877015,,,0004710,D056887,,,,
mondo:0000087,polymicrogyria,,0080918,,35981,C0266464,"['-0.1852', '0.2079', '0.3', '-0.4624', '0.316', '0.03592', '0.1565', '0.1655', '-0.644', '0.03009', '-0.6313', '-0.4219', '0.3938', '0.02632', '0.3281', '0.0003045', '0.01043', '-0.1562', '-0.1492', '-0.781', '0.2158', '0.10284', '0.335', '-0.2305', '0.02531', '-0.4294', '-0.07184', '0.11316', '-0.2291', '0.3354', '0.2861', '0.03595', '0.5225', '0.04767', '0.1104', '0.39', '-0.311', '-0.1671', '-0.1896', '-0.5054', '0.5483', '-0.418', '-0.02533', '-0.1309', '0.007866', '-0.7246', '0.282', '0.05835', '0.258', '0.2401', '0.341', '0.486', '-0.3425', '0.1251', '0.08075', '0.1218', '-0.015205', '0.2299', '-0.4275', '0.1901', '-0.1571', '-0.05246', '0.04532', '-0.1467', '-0.272', '0.3728', '0.2435', '0.1544', '-0.4253', '0.0934', '-0.2268', '0.3098', '0.4094', '0.0769', '-0.02881', '0.0888', '0.4973', '0.0737', '-0.257', '-0.4556', '-0.09863', '-0.2151', '0.178', '0.4233', '-0.05206', '-0.2942', '-0.2451', '0.07294', '0.48', '-0.2927', '0.1458', '0.2676', '-0.107', '0.0738', '0.0377', '-0.0954', '0.559', '-0.0759', '0.3838', '0.54']",C116936,,D065706,,,,
mondo:0000088,precocious puberty,"['pubertas praecox', 'familial precocious puberty', 'idiopathic sexual precocity', 'sexual precocity']",,,95708,C0034013,,C79704,,D011629,259.1,E30.1,10058084,0000826
mondo:0000090,progressive external ophthalmoplegia with mitochondrial DNA deletions,['progressive external ophthalmoplegia with mtDNA deletions'],,,,CN239267,,,,,,,,
mondo:0000093,"Schistosoma mansoni infection, susceptibility",,,,,,,,,,,,,
mondo:0000104,"anemia, hypochromic microcytic with iron overload","['anemia, hypochromic microcytic, with iron overload']",,,,C2673913,,,,C567144,,,,
mondo:0000105,"anemia, nonspherocytic hemolytic",,,,,,,,,,,,,
mondo:0000107,auriculocondylar syndrome,"['ears prominent and constricted', 'dysgnathia complex', 'auriculo-condylar syndrome', 'question mark ear syndrome', 'question mark ear', 'question-mark ear syndrome']",,,137888,CN160484,"['-0.1276', '0.1431', '0.2363', '-0.4219', '0.1527', '-0.4272', '0.2678', '0.6665', '-0.4768', '0.0501', '-0.2952', '-0.4475', '-0.01564', '-0.1111', '-0.1477', '0.1747', '0.1462', '-0.2463', '-0.298', '-0.4087', '0.08813', '-0.0975', '0.378', '-0.1088', '0.2242', '0.05328', '-0.6543', '0.06635', '0.4114', '-0.2852', '0.1794', '0.0803', '0.4226', '0.1746', '0.09894', '-0.11487', '-0.1241', '-0.04782', '-0.5586', '-0.6025', '-0.0824', '-0.1274', '0.04013', '-0.219', '-0.0924', '-0.125', '-0.1111', '0.3198', '-0.523', '0.4106', '-0.7354', '0.10645', '-0.00491', '0.0858', '-0.3926', '-0.357', '-0.02617', '-0.0503', '-0.005848', '0.0817', '0.1603', '0.11554', '-0.4775', '0.4514', '-0.0738', '-0.2769', '0.198', '0.335', '-0.2406', '0.569', '-0.4487', '0.44', '0.375', '-0.178', '-0.281', '-0.0888', '0.3157', '-0.3242', '-0.428', '-0.3162', '0.3062', '-0.2389', '0.02196', '0.819', '-0.0359', '0.1409', '-0.1641', '0.4695', '-0.05157', '0.04974', '0.2131', '0.5884', '-0.04123', '0.1682', '0.656', '0.06964', '0.531', '-0.3354', '0.3818', '0.2695']",,,C538270,,,,
mondo:0000108,"bacteremia, susceptibility",,,,,C3280646,,,,,,,,
mondo:0000110,bifid nose,,,,2695,CN227089,,,,C535441,,,,
mondo:0000111,"camptodactyly syndrome, Guadalajara",,,,,,,,,,,,,
mondo:0000114,cerebelloparenchymal disorder,,,,,,,,,,,,,
mondo:0000115,Chiari malformation,"['Chiari malformation', '(Arnold) Chiari malformation', 'Arnold-Chiari malformation']",,,,,,C84570,,D001139,,,,
mondo:0000118,reticulate pigment disorder,['reticulate pigment disorders'],,,,,,,,,,,,
mondo:0000119,"congenital heart defects, multiple types",['CHTD'],,,,,,,,,,,,
mondo:0000127,geleophysic dysplasia,"['geleophysic dwarfism syndrome', 'geleophysic dwarfism']",0111724,,2623,,"['-0.4998', '0.0825', '0.4626', '-0.2893', '-0.1915', '-0.4817', '0.2932', '0.7954', '-0.3188', '-0.653', '-0.001784', '-0.0389', '-0.149', '-0.1665', '-0.0916', '0.08185', '0.09467', '-0.3464', '-0.513', '-0.5215', '0.26', '0.191', '0.3684', '-0.03065', '0.2778', '-0.3723', '-0.2454', '0.04626', '0.2', '0.2015', '0.4998', '-0.3242', '0.158', '-0.5454', '0.12', '-0.3198', '-0.2366', '-0.2866', '0.2537', '-0.2612', '0.03027', '-0.1409', '0.1235', '0.3125', '0.3845', '-0.3005', '-0.1383', '0.24', '-0.5244', '-0.255', '-0.178', '0.6113', '-0.2183', '0.6616', '-0.036', '-1.16', '-0.0889', '-0.1344', '0.4868', '-0.1316', '0.421', '0.09204', '-0.8315', '-0.6284', '-0.4465', '-0.5327', '0.2874', '0.4507', '-0.7183', '0.07214', '-0.4963', '0.0415', '0.4143', '0.04114', '-0.3374', '0.3645', '-0.09863', '-0.2485', '-0.0707', '-0.00901', '0.409', '-0.3416', '0.4578', '0.1515', '-0.1575', '0.362', '-0.1779', '0.143', '0.5835', '0.14', '-0.05203', '0.1417', '-0.2482', '0.563', '0.4717', '0.728', '0.3044', '-0.6997', '0.4788', '0.4397']",,,,759.89,,10063361,
mondo:0000128,giant axonal neuropathy,,,,,C5200933,,C84728,,D056768,349.89,,,
mondo:0000129,glutaric aciduria,"['glutaric aciduria', 'glutaric acidemia', 'glutaric aciduria (disease)']",,,,C0268594,,,,,270.8,,,0003530
mondo:0000133,immunodeficiency-centromeric instability-facial anomalies syndrome,"['immunodeficiency-centromeric instability-facial anomalies', 'CIID', 'ICF syndrome', 'immunodeficiency-centromeric instability-facial anomalies syndrome']",0090007,,2268,CN201349,"['0.0411', '0.6064', '-0.1959', '-0.64', '0.549', '-0.1919', '0.1868', '0.2822', '-0.3574', '-0.0491', '-0.29', '0.4521', '0.3752', '0.2852', '0.0724', '0.2418', '0.0745', '-0.07416', '-0.3525', '-0.4385', '-0.2306', '-0.1483', '0.4246', '-0.11914', '0.4412', '-0.5146', '-0.2883', '-0.3289', '0.02289', '-0.3098', '0.8467', '0.5894', '0.1857', '0.1467', '0.1472', '-0.0882', '-0.7153', '-0.2693', '-0.4692', '0.2054', '0.01433', '0.1089', '0.4543', '-0.3174', '-0.103', '-0.3503', '-0.01052', '-0.456', '-0.318', '-0.4595', '-0.01167', '0.129', '-0.1177', '0.2294', '-0.0376', '-0.2327', '0.2032', '-0.4414', '0.0418', '0.604', '0.1887', '0.4678', '-0.232', '-0.1022', '0.51', '-0.6387', '0.3386', '-0.02399', '-0.414', '0.335', '-0.4607', '-0.2808', '0.0298', '-0.2269', '-0.03683', '0.297', '0.2612', '-0.153', '0.1067', '-0.1194', '0.304', '0.012726', '-0.03062', '0.03162', '-0.333', '0.3333', '0.1263', '0.4575', '0.5063', '-0.1311', '0.1791', '0.5728', '-0.05536', '-0.383', '0.5903', '0.7397', '0.1694', '-0.779', '0.224', '0.0459']",,,C537362,,,,
mondo:0000136,keratosis follicularis spinulosa decalvans,['keratosis pilaris decalvans'],0080753,,2340,,"['-0.3381', '0.3025', '3.69e-05', '-0.2446', '0.1895', '-0.4197', '-0.086', '0.07184', '-0.2057', '-0.01532', '-0.1605', '0.2676', '-0.237', '-0.0962', '-0.1952', '0.1279', '0.525', '-0.3455', '-0.09827', '-0.6016', '-0.3953', '-0.10175', '0.2491', '-0.03717', '0.06226', '0.3203', '-0.3022', '0.0753', '-0.2042', '-0.1819', '0.1957', '0.00483', '0.03946', '0.434', '0.2893', '0.1407', '-0.0693', '-0.128', '-0.1177', '-0.2568', '0.1355', '-0.1396', '0.00811', '-0.0627', '-0.10406', '-0.0831', '-0.1066', '0.348', '-0.08417', '-0.1013', '-0.1443', '-0.005573', '0.184', '0.1702', '-0.2178', '-0.2194', '0.521', '-0.2114', '-0.4106', '-0.2032', '0.2065', '0.09845', '-0.02724', '0.1881', '0.1466', '-0.01807', '0.678', '0.533', '0.072', '0.5522', '-0.4153', '-0.22', '0.272', '-0.005444', '0.05035', '-0.2751', '0.02446', '-0.1282', '0.2448', '-0.178', '0.3074', '-0.0406', '0.05865', '0.2166', '0.1418', '-0.1989', '-0.2808', '0.2488', '0.3484', '0.192', '0.3923', '0.378', '0.2964', '0.4346', '0.3386', '-0.1617', '0.4927', '-0.277', '0.2944', '0.2313']",,,,757.39,,,
mondo:0000137,"leukoencephalopathy, megalencephalic",,,,,,,,,,,,,
mondo:0000138,metaphyseal chondrodysplasia,"['metaphyseal chondrodysplasia', 'metaphyseal chondrodysplasia (disease)']",,,,,,,,,,,,0005871
mondo:0000141,mosaic variegated aneuploidy syndrome,"['Mosaic variegated aneuploidy syndrome 1', 'MVA1', 'Warburton-Anyane-Yeboa syndrome']",0080688,,1052,C1850343,"['0.00909', '-0.1361', '-0.187', '-0.0127', '0.2017', '-0.2874', '0.06946', '0.5303', '-0.4807', '-0.695', '-0.0655', '0.4097', '0.5312', '-0.2114', '-0.728', '-0.1113', '-0.491', '-0.51', '-0.1248', '-0.265', '0.1565', '0.0847', '0.01032', '-0.2216', '0.4958', '-0.1433', '-0.2048', '0.231', '0.2322', '-0.2167', '0.6', '0.2805', '1.177', '-0.3079', '0.3198', '0.2131', '-0.6006', '-0.2024', '-0.4087', '-0.279', '0.3176', '0.277', '0.3003', '-0.576', '-0.0924', '0.1656', '0.1042', '0.01735', '0.212', '-0.5356', '0.0513', '0.3074', '-0.11847', '0.07965', '-0.3804', '-0.4016', '0.1636', '0.00924', '-0.6562', '0.459', '0.4421', '-0.6157', '0.05194', '0.3994', '-0.1519', '0.03772', '0.6465', '0.04102', '-0.303', '-0.04858', '-0.0662', '0.3193', '-0.1521', '0.8604', '0.174', '-0.0737', '0.1879', '-0.2568', '-0.0907', '0.01106', '0.2352', '0.564', '-0.3982', '0.1776', '-0.2079', '-0.2778', '0.724', '0.3674', '0.2898', '-0.04184', '-0.1885', '0.6006', '-0.2192', '-0.2285', '0.571', '0.1538', '0.744', '-0.0409', '0.2089', '0.1439']",C128192,,C536987,758.89,,,
mondo:0000144,"pregnancy loss, recurrent, susceptibility",,,,,,,,,,,,,
mondo:0000147,polyposis,"['multiple polyps', 'polyposis']",,,,C0334108,,C4089,,,,,,
mondo:0000148,"pulmonary fibrosis and/or bone marrow failure, telomere-related",,,,,CN262497,,,,,,,,
mondo:0000151,symphalangism,,,,,,,,,,,,,
mondo:0000152,thiamine-responsive dysfunction syndrome,,,,,,,,,,,,,
mondo:0000153,transposition of the great arteries,"['transposition of great vessels', 'great vessels transposition', 'TGV', 'TGA', 'complete transposition', 'transposition of the great vessels']",,,216675,,,C84742,,D014188,,,,
mondo:0000155,triglyceride storage disease,"['inborn error of sequestering of triglyceride', 'rare inborn error of sequestering of triglyceride']",,,,,,,,,,,,
mondo:0000156,trigonocephaly,"['trigonocephaly, isolated', 'trigonocephaly', 'trigonocephalia', 'trigonocephalus']",,,,,,,,,,,,
mondo:0000158,developmental dysplasia of the hip,"['congenital hip dysplasia', 'congenital acetabular dysplasia', 'congenital dysplasia of the hip', 'dysplasia of acetabulum']",,,,C1840555,,,1000648,D000082602,755.63,,,
mondo:0000159,bone marrow failure syndrome,,,,,C2931245,"['-0.03888', '0.03784', '0.02118', '-0.01419', '0.04776', '-0.07477', '0.013954', '0.10724', '-0.0531', '-0.02908', '-0.01927', '-0.03', '-0.001156', '0.0233', '-0.03075', '-0.0515', '-0.00811', '-0.02785', '-0.02231', '-0.11285', '0.004204', '-0.02914', '0.07196', '-0.04947', '0.03336', '-0.0197', '-0.0113', '-0.0278', '-0.002533', '-0.02588', '0.04184', '-0.00834', '0.06104', '0.03033', '0.002167', '-0.03195', '-0.0196', '-0.05133', '-0.03558', '-0.0692', '0.001061', '-0.0379', '0.02844', '-0.04095', '-0.03378', '-0.07745', '-0.00913', '0.04114', '0.02336', '0.00106', '-0.02185', '-0.01391', '0.0567', '0.03503', '-0.02313', '-0.04773', '0.03793', '-0.01668', '-0.07135', '-0.00406', '0.0711', '0.02728', '-0.011475', '-0.03967', '-0.01229', '-0.0186', '0.08856', '0.06186', '-0.05624', '0.07684', '-0.0254', '0.002777', '0.00876', '-0.03827', '0.01555', '0.03705', '0.01962', '-0.002367', '-0.02338', '-0.03854', '-0.03577', '0.01593', '-0.04086', '0.0426', '-0.03078', '0.011024', '0.03198', '0.06256', '0.0689', '0.03033', '0.0279', '0.01451', '-0.01181', '0.01132', '0.1142', '0.05762', '0.0672', '-0.0967', '0.00737', '0.006527']",C165614,,C536572,,,,
mondo:0000160,"epilepsy, familial adult myoclonic",,0111689,,,,,,,,,,,
mondo:0000162,"autoimmune thyroid disease, susceptibility to",,,,,,,,,,,,,
mondo:0000166,"encephalopathy, acute, infection-induced",,,,,CN236791,"['-0.00515', '0.004078', '-0.01063', '-0.005108', '-0.008095', '-0.00833', '0.00796', '0.02713', '-0.02014', '0.00622', '-0.01116', '-0.001732', '-0.00698', '-0.0002377', '0.00126', '-0.013275', '-0.0005174', '-0.00502', '-0.00861', '-0.03046', '0.00643', '-0.01059', '0.00625', '-0.0174', '0.0114', '-0.01202', '0.001208', '0.001877', '-0.010185', '-0.000784', '0.009514', '0.00807', '0.01672', '-0.00247', '-0.005093', '0.007305', '-0.00658', '-0.003557', '-0.003452', '-0.0156', '0.011086', '-0.00989', '-0.003258', '-0.003784', '0.000892', '-0.015236', '-0.007446', '0.001262', '-0.005432', '0.01222', '-0.006325', '0.0003889', '0.007996', '0.002022', '-0.00794', '-0.004444', '0.013275', '-0.007286', '-0.01735', '-0.002905', '0.0004692', '0.01491', '0.0002942', '0.000148', '-0.01138', '0.01017', '0.015114', '0.018', '-0.005127', '0.01932', '-0.0004773', '0.007282', '0.000321', '-0.01173', '0.006573', '0.007347', '-0.0003426', '-0.005238', '-0.01105', '-0.000432', '-0.01036', '-0.00839', '-0.008156', '0.00797', '0.01267', '0.00885', '-0.002718', '0.02126', '0.02675', '0.00743', '0.003664', '0.01675', '0.002195', '0.001242', '0.03384', '0.01735', '0.01605', '-0.01569', '-0.001278', '-0.00315']",,,,,,,
mondo:0000167,Huntington disease and related disorders,,,,,,,,,,,,,
mondo:0000169,"microphthalmia, isolated, with cataract",,,,,,,,,,,,,
mondo:0000170,"microphthalmia, isolated, with coloboma","['colobomatous microphthalmia', 'microphthalmia associated with colobomatous cyst', 'microphthalmos bilateral, colobomatous orbital cyst', 'microphthalmia-anophthalmia-coloboma syndrome', 'MAC', 'microphthalmia with colobomatous cyst', 'MCOPCB1']",,,98938,CN228419,"['-0.2656', '-0.03516', '0.1814', '-0.11304', '0.1323', '-0.04834', '0.06143', '0.179', '-0.3418', '-0.2112', '-0.08105', '-0.2264', '-0.12', '-0.1021', '-0.3755', '-0.1813', '0.2294', '-0.2286', '0.08405', '-0.6196', '-0.03403', '0.00556', '0.2284', '-0.1902', '0.1643', '-0.0186', '-0.224', '0.07025', '0.3044', '0.1678', '0.1014', '0.0184', '0.3025', '0.2776', '0.0352', '0.0889', '0.1567', '-0.1032', '-0.11285', '-0.3567', '0.39', '-0.1506', '0.02028', '-0.348', '-0.04492', '-0.1879', '0.01', '0.2773', '0.1395', '0.1442', '-0.1844', '0.02968', '0.05334', '-0.2263', '-0.1348', '-0.1816', '0.2157', '-0.0985', '-0.3945', '0.005596', '0.1469', '-0.05167', '0.0681', '0.0948', '-0.1093', '-0.0668', '0.2842', '0.5415', '-0.2241', '0.2147', '-0.2146', '0.2634', '0.1311', '-0.05295', '0.002926', '-0.1251', '0.2888', '-0.1138', '-0.1934', '-0.1259', '0.02739', '0.1262', '-0.00964', '0.6113', '-0.11633', '-0.4253', '-0.01192', '0.3433', '0.10077', '0.3108', '-0.02745', '0.551', '0.155', '0.05563', '0.618', '-0.2164', '0.3882', '-0.2632', '0.09564', '0.2666']",,,C537463,,,,
mondo:0000171,"muscular dystrophy-dystroglycanopathy, type A","['Walker-Warburg syndrome', 'Warburg syndrome', 'Pagon syndrome', 'hard +/- E syndrome', 'hard syndrome', 'hydrocephalus-agyria-retinal dysplasia syndrome', 'WWS', 'hydrocephalus, agyria and retinal dysplasia', 'Chemke syndrome', 'cerebroocular dysplasia-muscular dystrophy syndrome', 'Walker-Warburg muscular dystrophy', 'cerebroocular dysplasia muscular dystrophy syndrome', 'cerebroocular dysgenesis']",0050560,,899,CN239483,"['-0.01857', '-0.816', '-0.675', '-0.1418', '0.548', '-1.108', '0.10596', '0.696', '-1.659', '-0.8613', '-0.1455', '-0.12305', '-0.3274', '0.4648', '0.3547', '0.1598', '-0.765', '-0.672', '-0.558', '-0.607', '-0.1295', '0.2832', '0.3735', '0.3716', '-0.04367', '-0.3923', '-0.1436', '-0.7266', '0.2676', '-0.2952', '0.6875', '0.1896', '0.626', '-0.175', '0.05035', '0.06216', '-0.3801', '0.1962', '0.3176', '-0.2612', '0.1166', '-0.305', '-0.3745', '0.1445', '-0.1736', '0.4277', '-0.02097', '0.722', '-0.1277', '0.1735', '0.698', '-0.2163', '0.3828', '-0.8545', '-0.004776', '-0.3809', '0.481', '0.6562', '-0.525', '0.05502', '-0.2391', '-0.2937', '-0.3425', '0.03394', '-0.09894', '-0.1575', '0.0467', '0.2212', '-0.565', '0.02493', '-0.391', '0.6533', '-0.0748', '-0.12415', '0.7', '0.4888', '0.06744', '0.4106', '-0.01675', '0.1926', '0.3945', '-0.1515', '-0.4353', '0.354', '-0.3906', '0.1077', '0.05545', '-0.015594', '0.9434', '0.295', '-0.1758', '0.4485', '0.2883', '0.8003', '-0.3748', '-0.0431', '0.2656', '-0.462', '0.188', '0.02664']",C99109,,D058494,,,,
mondo:0000172,"muscular dystrophy-dystroglycanopathy, type B",,0112375,,,CN228400,,,,,,,,
mondo:0000173,"muscular dystrophy-dystroglycanopathy, type C",,,,,CN262500,,,,,,,,
mondo:0000179,Neu-Laxova syndrome,"['nuclear localization signal', 'NLS', 'Neu Laxova syndrome']",,,2671,C0265218,"['-0.3845', '0.452', '0.24', '-0.624', '0.3547', '-0.1923', '-0.2964', '0.2351', '-0.545', '-0.3052', '-0.04468', '-0.46', '-0.4495', '-0.318', '-0.2766', '-0.06665', '0.3594', '-0.1893', '-0.11945', '-0.3313', '-0.04437', '0.01845', '0.1137', '-0.1277', '-0.0692', '0.1268', '-0.4727', '0.2434', '0.658', '-0.4827', '0.05026', '-0.0883', '0.427', '0.1481', '0.04117', '0.05145', '-0.2156', '0.14', '-0.41', '-0.126', '0.2119', '-0.3713', '-0.0925', '0.10345', '-0.0758', '-0.4583', '0.283', '0.3062', '-0.2369', '-0.3835', '0.1321', '-0.366', '-0.1902', '-0.398', '-0.9126', '-0.1913', '-0.0765', '0.09424', '0.07684', '0.0863', '-0.1702', '0.0693', '-0.4128', '0.6953', '-0.0833', '-0.3472', '0.3865', '0.3643', '-0.7', '0.503', '-0.6616', '0.71', '0.1746', '0.000978', '-0.4058', '0.3472', '0.3237', '0.1829', '-0.4443', '-0.3062', '0.0706', '0.04825', '0.06384', '0.4666', '-0.1133', '-0.1287', '0.0551', '0.3523', '-0.2456', '0.1914', '0.3403', '0.0079', '0.6167', '0.00211', '0.733', '0.412', '0.2344', '-0.4739', '0.7817', '0.1542']",C14089,,C536405,759.89,,,
mondo:0000181,microcephaly and chorioretinopathy,,,,,,,,,,,,,
mondo:0000182,congenital myasthenic syndrome with tubular aggregates,"['CMS-TA', 'myasthenic syndrome, congenital, with tubular aggregates']",,,,CN228621,,,,,,,,
mondo:0000188,GLUT1 deficiency syndrome,['GLUT1DS'],,,,,,,,,,,,
mondo:0000190,ventricular fibrillation,"['fibrillation, ventricular', 'ventricular fibrillation', 'VF', 'VFib', 'ventricular fibrillation (disease)']",,,,C0042510,,C50799,0004287,D014693,427.41,,,0001663
mondo:0000192,polyglucosan body myopathy,,,,,CN228160,,,,,,,,
mondo:0000193,cortisone reductase deficiency,"['CORTRD', 'HSD 11B1 deficiency', 'deficiency of (R)-20-hydroxysteroid dehydrogenase', 'deficiency of cortisone reductase', '11-alpha beta-hydroxysteroid dehydrogenase type I deficiency of', '11-beta-hydroxysteroid dehydrogenase deficiency type 1']",0090139,,168588,CN200166,"['-0.877', '0.2747', '0.09314', '-0.2311', '0.2517', '-0.0198', '-0.2231', '0.696', '-0.0341', '-0.3171', '-0.1577', '0.1392', '-0.0806', '0.491', '0.105', '-0.3855', '0.145', '0.2998', '-0.544', '-0.3115', '-0.01039', '-0.5254', '0.442', '-0.2847', '0.11', '0.02586', '0.1697', '-0.3608', '0.114', '-0.5225', '0.4807', '-0.1027', '0.4783', '0.2268', '-0.0681', '-0.1726', '0.1027', '-0.01663', '-0.2908', '-0.3533', '0.5356', '0.1774', '0.2197', '-0.1707', '0.1129', '-0.568', '0.2153', '-0.03067', '-0.1595', '0.569', '0.228', '-0.01361', '0.0904', '0.383', '-0.224', '0.04562', '0.4578', '-0.494', '-0.1517', '0.1244', '0.2142', '0.4336', '0.2869', '-0.0573', '0.0819', '0.2856', '0.3298', '0.5293', '-0.2319', '0.06647', '-0.3313', '-0.001976', '0.3115', '0.1631', '-0.1516', '-0.37', '-0.1577', '0.03156', '-0.01304', '-0.1176', '-0.02141', '0.3232', '0.0797', '-0.04535', '0.1288', '0.3535', '0.1687', '-0.4155', '0.846', '-0.010704', '-0.0829', '0.32', '-0.2081', '-0.2456', '0.271', '-0.2566', '0.3196', '-0.1611', '0.04633', '0.1783']",,,C536447,277.6,,,
mondo:0000200,Zimmermann-Laband syndrome,"['ZLS1', 'gingival fibromatosis-hepatosplenomegaly-other anomalies syndrome', 'Laband syndrome', 'Zimmermann-Laband syndrome 1', 'ZLS', 'Zimmerman Laband syndrome', 'fibromatosis gingival, hepatosplenomegaly other anomalies', 'Zimmermann-Laband syndrome type 1', 'gingival fibromatosis, abnormal fingers, fingernails, nose and ears, and splenomegaly', 'Laband-Zimmermann syndrome']",,,3473,C0796013,"['-0.1526', '0.0428', '0.543', '-0.1693', '0.4236', '-0.3496', '-0.2179', '0.8022', '-0.5522', '-0.01495', '-0.2622', '0.1421', '-0.04056', '-0.0625', '-0.0998', '0.03745', '0.527', '-0.521', '-0.4746', '-0.391', '0.074', '-0.0575', '0.5137', '-0.1078', '0.1951', '0.01234', '-0.5415', '0.11176', '0.348', '-0.2245', '0.283', '-0.06354', '-0.05853', '0.2861', '0.336', '-0.965', '-0.753', '-0.1772', '-0.01137', '-0.3652', '0.2896', '-0.2554', '-0.1632', '-0.534', '0.6523', '-0.571', '-0.1832', '0.5625', '-0.158', '-0.2034', '-0.3665', '0.1103', '0.6797', '0.0415', '-0.7397', '-0.2573', '-0.2087', '0.03525', '-0.2172', '-0.3723', '-0.1107', '-0.153', '-0.168', '-0.3572', '-0.2737', '0.1061', '0.1185', '0.3967', '-0.1506', '-0.03214', '-0.454', '-0.3826', '0.603', '-0.1664', '-0.153', '-0.03268', '0.2622', '-0.3306', '-0.08624', '-0.1615', '0.6235', '-0.05792', '0.03336', '0.3428', '0.03323', '0.2166', '-0.4524', '0.6226', '0.2416', '0.5576', '0.342', '0.579', '0.09186', '0.2263', '0.1985', '-0.02408', '0.2424', '-0.836', '0.728', '0.7837']",,,C536725,759.89,,,
mondo:0000208,"microcephaly, short stature, and impaired glucose metabolism 1","['MSSGM', 'MSSGM1', 'microcephaly, short stature, and impaired glucose metabolism', 'microcephaly, short stature, and impaired glucose metabolism 1']",,616033,,C4014997,,,,,,,,
mondo:0000209,prenatal-onset spinal muscular atrophy with congenital bone fractures,['SMABF'],,,486811,CN238807,,,,,,,,
mondo:0000210,thiopurine metabolic disease,,,,,,,,,,,,,
mondo:0000211,"striatal degeneration, autosomal dominant","['ADSD', 'autosomal dominant striatal neurodegeneration']",,,228169,C1836694,"['-0.5054', '0.0783', '-0.1892', '-0.2856', '-0.1454', '-0.789', '-0.0797', '0.6133', '-0.336', '-0.2283', '-0.00825', '-0.05493', '-0.1663', '-0.2837', '0.4106', '0.3628', '0.0893', '-0.672', '-0.2708', '-0.954', '-0.2216', '-0.3594', '-0.3774', '-0.0438', '0.3206', '0.1919', '0.3323', '0.07446', '-0.6', '0.4143', '0.1897', '0.2054', '0.04773', '-0.006115', '0.1556', '0.01562', '-0.1876', '-0.621', '0.2588', '0.03177', '0.5347', '-0.4685', '-0.2417', '0.2556', '0.5566', '-0.04834', '-0.3464', '-0.2096', '-0.396', '0.01411', '0.1469', '0.0703', '-0.5635', '-0.02847', '0.2764', '-0.0992', '0.4155', '-0.06915', '-0.3013', '0.1505', '0.00598', '0.01752', '0.1154', '-0.4155', '-0.7646', '0.05048', '0.537', '0.1827', '-0.2656', '0.5474', '-0.3699', '0.02823', '-0.3796', '-0.2703', '0.489', '0.2343', '-0.02878', '-0.11316', '0.0691', '-0.2026', '0.5107', '-0.2072', '0.3381', '0.6646', '0.2281', '0.167', '-0.3364', '0.355', '0.55', '-0.1932', '0.2795', '0.2302', '-0.2157', '-0.1077', '0.4253', '0.2424', '0.342', '-0.1265', '0.2393', '0.1205']",,,C563783,,,,
mondo:0000212,"hypercalcemia, infantile","['infantile hypercalcemia', 'autosomal recessive infantile hypercalcemia', 'familial infantile hypercalcemia with suppressed intact parathyroid hormone', 'autosomal recessive hypercalcemia, infantile', 'hypercalcemia, infantile', 'hypercalcemia, infantile, autosomal recessive', 'infantile hypercalcemia disease', 'idiopathic infantile hypercalcemia', 'hypercalcemia, idiopathic, of infancy', 'hypercalcemia disease of infancy', 'infantile onset hypercalcemia disease']",,,300547,CN203398,"['0.06805', '0.1159', '0.639', '0.16', '-0.1733', '0.0566', '-0.2277', '0.6367', '-0.579', '-0.272', '0.0774', '0.377', '-0.9365', '0.7217', '-0.0605', '-0.8154', '-0.5576', '0.2805', '-0.2369', '-0.3342', '0.4082', '-0.5557', '-0.3103', '-0.765', '0.6396', '-0.582', '0.4805', '-0.7227', '0.0336', '-0.4685', '0.0609', '0.0942', '0.3586', '-0.11945', '-0.8145', '-0.6196', '-0.3354', '0.0222', '0.33', '-0.3948', '-0.0514', '-0.2742', '0.1776', '-0.559', '0.5806', '-0.4937', '0.1167', '0.02399', '-0.1013', '0.637', '-0.1076', '0.726', '0.532', '-0.11755', '-0.7783', '0.04706', '-0.5435', '0.603', '0.06015', '0.388', '0.4363', '0.0938', '-0.1241', '-0.5312', '-0.719', '0.02576', '0.2257', '0.688', '-0.5015', '-0.03024', '0.2808', '0.4036', '0.326', '-0.2415', '-0.11957', '1.133', '-0.2074', '1.181', '0.7505', '0.3696', '-0.784', '-0.4863', '0.1421', '0.0783', '0.328', '0.02121', '0.2362', '0.121', '0.7324', '0.4282', '-0.06082', '0.2151', '-0.532', '-0.0764', '0.735', '1.004', '0.1029', '-0.4612', '-0.5635', '0.1924']",C129734,,C562999,,,,
mondo:0000213,"autoimmune disease, multisystem, infantile-onset",,,,,CN238808,,,,,,,,
mondo:0000214,hypermanganesemia with dystonia,,0080535,,,,,,,,,,,
mondo:0000222,seminal vesicle acute gonorrhea,"['acute gonococcal seminal vesiculitis', 'gonococcal seminal vesiculitis, acute']",0050004,,,C0153194,,,,,,,,
mondo:0000224,acquired carbohydrate metabolism disease,['carbohydrate metabolism disease'],0050013,,,,,,,,,,,
mondo:0000225,human monocytic ehrlichiosis,"['Human ehrlichial infection, human monocytic type', 'ehrlichiosis chafeensis', 'HME']",0050026,,,C1282983,,,,,082.41,,,
mondo:0000226,mineral metabolism disease,,,,,,,,,,275.9,E83,,
mondo:0000227,African tick-bite fever,"['South African tick-bite fever', 'Rickettsia africae spotted fever']",0050035,,,C1320317,,,,,,,,
mondo:0000229,Indian tick typhus,,0050042,,101335,,,,,,,,,
mondo:0000230,Israeli tick typhus,['Israeli spotted fever'],0050043,,,,,,,,,,,
mondo:0000231,Far eastern spotted fever,['Rickettsia heilongjiangensis spotted fever'],0050046,,,C3532354,,,,,,,,
mondo:0000232,Flinders island spotted fever,"['FISF', 'Thai tick typhus']",0050047,,,C4505102,,,,,,,,
mondo:0000233,Japanese spotted fever,"['fever, Japanese spotted', 'fevers, Japanese spotted', 'Rickettsia japonica spotted fever', 'Japanese spotted fever', 'Japanese spotted fevers', 'oriental spotted fever', 'spotted fever, Japanese']",0050050,,,C2108396,,,,,,,,
mondo:0000234,Rickettsia parkeri spotted fever,['maculatum infection'],0050051,,,,,,,,,,,
mondo:0000236,oropharyngeal anthrax,['oropharynx anthrax infection'],0050059,,,,,,,,,,,
mondo:0000239,adiaspiromycosis,"['adiaspirosis', 'adiaspiromycosis', 'pulmonary adiaspiromycosis', 'haplosporangiosis']",0050072,,,C0259737,,,,C000656784,117.9,,,
mondo:0000240,invasive aspergillosis,,0050073,,,C0238013,,,,,,,,
mondo:0000241,Keshan disease,"['congestive cardiomyopathy due to selenium deficiency', 'enlarged heart and poor heart function']",0050083,,,C0268095,,,,C536166,269.3,,,
mondo:0000242,tinea barbae,"['dermatophytosis of beard', 'beard dermatophytosis']",0050096,,,C2349994,,,,C000656825,,,,
mondo:0000243,ectothrix infectious disease,,0050097,,,,,,,,,,,
mondo:0000244,endothrix infectious disease,,0050105,,,,,,,,,,,
mondo:0000245,tinea imbricata,,0050116,,,C0040255,,,,,,B35.5,,
mondo:0000248,dengue shock syndrome,['DSS'],0050125,,,C0376300,,,,D019595,,,,
mondo:0000249,secretory diarrhea,,0050129,,,C0267557,,,,,,,,0005208
mondo:0000250,osmotic diarrheal disease,"['osmotic diarrhoea', 'permeability diarrhea', 'permeability diarrhoea']",0050130,,,C0267556,,,,,,,,
mondo:0000251,diarrheal disease secondary to altered bowel motility,"['motility-related diarrhoea', 'diarrhea secondary to altered bowel motility', 'diarrhoea secondary to altered bowel motility']",,,,,,,,,,,,
mondo:0000252,inflammatory diarrhea,,0050132,,,,,,,,,,,
mondo:0000253,piedra,"['piedra, White', 'steroid-modified tinea infection', 'piedra, black', 'hair shaft fungal infectious disease', 'black Piedras', 'black piedra', 'Piedras, black', 'Piedras, White', 'White piedra', 'White Piedras', 'Piedras']",,,,C0031898,,,,D010854,,,,
mondo:0000254,cutaneous mycosis,,0050134,,,,,,,,,,,
mondo:0000255,subcutaneous mycosis,,0050135,,,,,,,,,,,
mondo:0000256,systemic mycosis,['systemic fungal infection'],0050136,,,C0553576,,,,,117.9,,,
mondo:0000257,acute diarrhea,"['acute diarrheal disease', 'diarrheal disease, acute', 'diarrhea, acute', 'diarrhoea (disease), acute', 'diarrhea (disease), acute']",0050140,,,C0740441,,,,,,,,
mondo:0000259,asymptomatic dengue,,0050143,,,,,,,,,,,
mondo:0000261,adenoiditis,"['pharyngeal tonsil inflammation', 'chronic adenoiditis', 'pharyngeal tonsilitis']",0050145,,,C0396023,,,,,474.01,J35.02,,
mondo:0000262,otomycosis,"['external ear fungal infectious disease', 'Singapore ear', 'otitis mycotic externa']",0050147,,,C0029895,,,,D059249,111.8,,,
mondo:0000263,laryngotracheitis,,0050148,,,C0023076,,,,,476.1,,,
mondo:0000265,aspiration pneumonia,"['aspiration pneumonia', 'acid aspiration syndrome', 'syndrome, acid aspiration', 'Mendelson^s syndrome', 'gastric acid aspiration syndrome', 'syndrome, Mendelson^s', 'syndromes, acid aspiration', 'aspiration pneumonia (disease)', 'acid aspiration syndromes', 'Mendelson syndrome', 'Pneumonias, aspiration', 'inhalation pneumonia', 'Mendelsons syndrome', 'syndrome, Mendelson', 'aspiration Pneumonias']",0050152,,,C0085740,,,,D011015,,,,0011951
mondo:0000266,pulmonary aspergilloma,['lung aspergillosis'],0050153,,,C2350529,,,,D055732,,,,
mondo:0000270,lower respiratory tract disorder,"['disease of lower respiratory tract', 'lower respiratory tract disease', 'disorder of lower respiratory tract', 'lower respiratory tract disease or disorder']",0050161,,,C1290325,,,,,478.19,,,
mondo:0000271,tuberculous salpingitis,['fallopian tube tuberculosis'],0050166,,,C0275933,,,,,016.60,,,
mondo:0000273,Kunjin virus infectous disease,['Kunjin encephalitis'],0050174,,,,,,,,,,,
mondo:0000276,Powassan encephalitis,"['encephalitis, powassan', 'Powassan virus caused disease or disorder', 'powassan encephalitis virus infection']",0050179,,,C1563215,,,,,063.8,,,
mondo:0000282,Whitewater Arroyo hemorrhagic fever,,0050199,,,,,,,,,,,
mondo:0000283,"Hantavirus hemorrhagic fever with renal syndrome, Seoul virus type",['Korean hemorrhagic fever'],0050200,,,,,,,,,,,
mondo:0000284,"Hantavirus hemorrhagic fever with renal syndrome, Puumala virus type","['nephropathis epidemica', 'nephropathia epidemica']",0050201,,,C0242993,,,,,,,,
mondo:0000286,Epstein-Barr virus hepatitis,,0050204,,,C0554114,,,,,,,,
mondo:0000288,polycystic echinococcosis,"['neotropical echinococcosis', 'human polycystic hydatid disease']",0050218,,,,,,,,,,,
mondo:0000290,primary amebic meningoencephalitis,"['Naegleria fowleri infection', 'infections, Naegleria fowleri']",0050242,,,C4303098,,,,C535275,,,,
mondo:0000291,granulomatous amebic encephalitis,"['granulomatous amoebic encephalitis', 'Acanthamoeba encephalitis', 'granulomatous amebic encephalitis due to Acanthamoeba', 'Acanthamoeba granulomatous encephalitis']",0050246,,,C0338428,,,,,323.2,,,
mondo:0000292,philophthalmiasis,['Philophthalmus caused disease or disorder'],0050250,,,,,,,,,,,
mondo:0000293,coenurosis,"['sturdy', 'caenurosis']",0050251,,,C0009225,,,,,123.8,,,
mondo:0000294,mesocestoidiasis,['Mesocestoides caused disease or disorder'],0050253,,,C0277110,,,,,,,,
mondo:0000295,acanthocephaliasis,['Acanthocephala caused disease or disorder'],0050254,,,C0277331,,,,,,,,
mondo:0000297,baylisascariasis,"['raccoon roundworm infection', 'Baylisascaris procyonis caused disease or disorder']",0050259,,,C0277150,,C128397,,,,,,
mondo:0000298,dioctophymiasis,['Dioctophyme renale caused disease or disorder'],0050260,,,C0012482,,,,,,,,
mondo:0000299,thelaziasis,['Thelazia caused disease or disorder'],0050261,,,C0344058,,,,,128.8,,,
mondo:0000301,ophthalmomyiasis,['Oestrus ovis caused myiasis'],0050268,,,C0027034,,,,,,,,
mondo:0000302,basidiobolomycosis,"['basidiobolomycosis', 'Basidiobolus caused disease or disorder', 'infection by Basidiobolus', 'infection caused by Basidiobolus']",0050278,,,C0343965,,,,,,,,
mondo:0000303,conidiobolomycosis,,0050279,,,C0276712,,,,,111.8,,,
mondo:0000304,penicilliosis,['Talaromyces marneffei caused disease or disorder'],0050288,,,C1274008,,,,,,,,
mondo:0000306,trichosporonosis,['Trichosporon caused disease or disorder'],0050290,,,C0343939,,,,D060586,,,,
mondo:0000307,parasitic Ichthyosporea infectious disease,['Ichthyosporea caused disease or disorder'],0050291,,,,,,,,,,,
mondo:0000308,primary systemic mycosis,,0050292,,,,,,,,,,,
mondo:0000309,aniseikonia,,0050304,,,,,,1001266,D000839,367.32,H52.32,,
mondo:0000310,Alkhurma hemorrhagic fever,['Alkhumra hemorrhagic fever virus caused disease or disorder'],0050308,,,,,,,,,,,
mondo:0000313,hypophosphatemia,"['hypophosphatemia (disease)', 'hypophosphatemia']",0050336,,,C0085682,,C37977,,D017674,,,,0002148
mondo:0000314,primary bacterial infectious disease,,0050338,,,,,,,,,,,
mondo:0000315,commensal bacterial infectious disease,,0050339,,,,,,,,,,,
mondo:0000316,opportunistic bacterial infectious disease,,0050340,,,,,,,,,,,
mondo:0000320,glandular tularemia,['lymph node tularemia'],0050382,,,C0275974,,,,,,,,
mondo:0000321,typhoidal tularemia,,0050383,,,C0473876,,,,,,,,
mondo:0000327,Buruli ulcer disease,"['Buruli ulcer', 'Searle^s ulcer', 'Daintree ulcer', 'Bairnsdale ulcer', 'Searl ulcer', 'Mossman ulcer', 'Mycobacterium ulcerans caused disease or disorder']",0050456,,,C0085568,"['-0.0893', '0.05658', '-0.00819', '-0.2216', '-0.0203', '-0.1805', '0.1153', '-0.02296', '-0.0874', '0.0497', '-0.04156', '0.1844', '-0.07654', '0.0726', '-0.2463', '0.02046', '-0.04224', '-0.1137', '-0.0807', '-0.352', '-0.1234', '-0.21', '0.1836', '-0.268', '0.02147', '0.0855', '-0.1025', '0.2068', '-0.1554', '-0.06506', '0.1188', '0.00771', '0.04865', '0.00863', '0.02513', '0.09576', '-0.2079', '-0.01489', '-0.0556', '-0.23', '-0.0848', '-0.1528', '0.2825', '-0.1263', '0.03412', '-0.10956', '-0.1945', '0.0789', '0.1549', '0.0799', '-0.12067', '-0.02682', '0.3066', '0.2108', '-0.07196', '-0.0932', '0.287', '-0.11774', '-0.3972', '-0.07825', '0.10803', '0.2003', '-0.1846', '-0.03583', '0.1641', '-0.0997', '0.3467', '0.2798', '-0.0722', '0.3208', '-0.2583', '-0.05728', '0.06744', '-0.0823', '0.0726', '0.0413', '0.2227', '0.1935', '0.0885', '-0.2439', '-0.219', '-0.2457', '0.001096', '-0.01455', '0.02301', '-0.06195', '0.08167', '0.0791', '0.1027', '-0.05612', '0.1562', '0.2615', '0.00452', '0.1277', '0.453', '0.2262', '0.2069', '-0.1725', '0.031', '-0.0218']",C84604,1001281,D054312,,,,
mondo:0000328,hyperphosphatemia,"['hyperphosphatemia', 'hyperphosphatemia (disease)']",0050459,,,C0085681,,,,D054559,,,,0002905
mondo:0000330,endemic typhus,"['rat-flea typhus', 'endemic flea-borne typhus', 'shop typhus', 'urban typhus', 'urban typhus of Malaya', 'cat flea rickettsiosis', 'fleaborne typhus', 'murine typhus', 'endemic typhus fever', 'toulon typhus', 'Rickettsia felis spotted fever']",0050481,,83315,CN206047,,C84688,,D014437,,,10028282,
mondo:0000331,Rickettsia helvetica spotted fever,"['Rickettsia helvetica caused disease or disorder', 'aneruptive fever', 'Rickettsia helvetica aneruptive fever']",0050484,,,,,,,,,,,
mondo:0000332,sennetsu fever,"['Neorickettsia sennetsu caused disease or disorder', 'sennetsu fever', 'Human Ehrlichial infection, sennetsu type', 'sennetsu ehrlichiosis']",0050485,,,C0520779,,,,C537582,088.89,,,
mondo:0000333,early congenital syphilis,['Early congenital syphilis (less than 2 years)'],0050488,,,C0275859,,,,,090.2,,,
mondo:0000334,multinodular goiter,"['goiter, multinodular']",0050489,,,C0342208,,C131438,,,,,,
mondo:0000335,parenchymatous neurosyphilis,,0050490,,,,,,,,,,,
mondo:0000336,meningovascular neurosyphilis,,0050491,,,,,,,,,,,
mondo:0000337,exanthema subitum,"['roseola', 'sixth disease', 'exanthem subitum', 'roseola Infantum']",0050495,,,C0595993,,C128420,1001320,D005077,058.10,,,
mondo:0000338,variola major infectious disease,,0050508,,,C1812609,,,,,050.0,,,
mondo:0000339,spinal polio,,0050513,,,,,,,,,,,
mondo:0000340,bulbospinal polio,,0050514,,,,,,,,,,,
mondo:0000341,paralytic poliomyelitis,,0050515,,,,,,,,,,,
mondo:0000342,O^nyong^nyong fever,['O^nyong-nyong virus caused disease or disorder'],0050516,,,C0276286,,,,,,A92.1,,
mondo:0000343,Barmah forest virus disease,['Barmah Forest virus caused disease or disorder'],0050517,,,,,,,,,,,
mondo:0000344,Ross river fever,"['Ross River virus caused disease or disorder', 'Ross River virus disease']",0050518,,,C0035865,,,,,,,,
mondo:0000345,Oropouche fever,['Oropouche virus caused disease or disorder'],0050521,,,C0276386,,,,,,,,
mondo:0000346,"Hantavirus hemorrhagic fever with renal syndrome, Dobrava-Belgrade virus type",['Balkan hemorrhagic fever'],0050522,,,,,,,,,,,
mondo:0000351,disorder of methionine catabolism,"['inborn error of methionine catabolic process', 'hypermethioninemia', 'rare inborn error of methionine catabolic process']",0050544,,,C4048705,,,,,,,,0003235
mondo:0000355,Ullrich congenital muscular dystrophy,"['late onset scleroatonic familial myopathy (subtype)', 'Ullrich disease', 'Ullrich scleroatonic muscular dystrophy', 'UCMD', 'scleroatonic Ullrich disease', 'congenital muscular dystrophy, Ullrich type', 'scleroatonic muscular dystrophy']",0050558,,75840,C0410179,"['0.1066', '-0.677', '-0.8545', '-0.1946', '0.457', '-1.28', '-0.01913', '0.606', '-1.613', '-0.8037', '0.0714', '0.3335', '-0.127', '0.655', '-0.01276', '0.4712', '-0.5444', '-0.396', '-0.3545', '-0.8423', '-0.1526', '0.0679', '0.1575', '0.11896', '-0.0121', '-0.2407', '0.2086', '-0.542', '-0.1003', '-0.4065', '0.677', '0.09094', '0.3975', '0.1804', '0.131', '-0.2405', '-0.2698', '0.1688', '0.05502', '-0.2385', '-0.07806', '-0.1692', '-0.2413', '0.55', '0.10626', '0.2186', '-0.01753', '0.6343', '-0.08673', '0.2203', '0.259', '-0.3752', '0.3699', '-0.47', '-0.004593', '-0.252', '0.1185', '1.013', '-0.1508', '-0.1603', '0.2505', '0.139', '-0.1912', '0.2622', '0.1126', '-0.09845', '-0.10706', '0.6787', '-0.1821', '0.005917', '-0.1309', '-0.2773', '-0.01171', '-0.2625', '0.7363', '0.6157', '0.05194', '0.266', '-0.0077', '0.225', '0.2186', '-0.3408', '-0.1675', '0.1781', '-0.2317', '0.4756', '-0.257', '-0.2086', '0.398', '0.0997', '-0.2583', '0.08905', '0.0687', '0.88', '-0.09534', '-0.0993', '0.4482', '-0.6514', '0.1964', '0.1671']",C123438,,C537521,,,,
mondo:0000358,orofacial cleft,,0050567,,,CN221583,,,,,,,,
mondo:0000359,spondylocostal dysostosis,"['spondylocostal dysostosis', 'Jarcho-Levin syndrome', 'SCD', 'SCDO', 'spondylocostal dysplasia', 'costovertebral dysplasia']",0050568,,1797,CN201467,"['-1.005', '0.0301', '0.4526', '-0.23', '0.463', '-0.1709', '-0.03256', '0.2107', '-0.4685', '-0.391', '-0.1926', '0.03305', '-0.1884', '-0.1882', '-0.10803', '-0.2476', '0.0937', '0.1208', '-0.2375', '-0.6807', '-0.1509', '0.4248', '0.5254', '-0.1691', '0.2607', '0.1136', '-0.00823', '-0.3105', '0.2146', '-0.1964', '0.0762', '-0.1285', '-0.001062', '0.3767', '0.0703', '-0.2476', '-0.2308', '-0.369', '-0.08203', '-0.486', '0.2283', '-0.4993', '0.4614', '-0.1599', '-0.148', '-0.517', '-0.4958', '0.44', '0.1879', '0.103', '0.4026', '0.01437', '-0.02805', '-0.001275', '-0.354', '-0.672', '-0.08997', '0.0194', '0.07794', '0.04077', '0.0388', '-0.0632', '-0.1469', '-0.1858', '-0.2183', '-0.1133', '0.1947', '0.3674', '-0.187', '0.1907', '-0.1103', '-0.03925', '0.3381', '-0.2283', '-0.08716', '0.303', '-0.1383', '-0.3792', '-0.2698', '-0.3015', '-0.2452', '-0.1791', '-0.05353', '0.4893', '-0.0444', '0.123', '-0.153', '0.2815', '-0.05154', '-0.09827', '-0.0709', '0.1289', '0.01229', '0.0964', '0.6943', '0.09216', '0.816', '-0.6084', '0.066', '0.143']",C125598,,C537565,,,,
mondo:0000363,gummatous syphilis,,0050584,,,,,,,,,,,
mondo:0000365,primary congenital glaucoma,"['primary congenital glaucoma (disease)', 'primary congenital glaucoma']",0050593,,,C3888011,,C150251,,,,,,0008007
mondo:0000367,taeniasis,"['unarmed tapeworm infection', 'infection by taenia saginata', 'Taenia saginata infectious disease', 'Taenia infection', 'infection by Taeniarhynchus saginatus', 'taenia saginata infection', 'infections, Taenia', 'beef tapeworm infection']",0050596,,,C0152073,,C85180,1001433,D013622,123.2,B68,,
mondo:0000368,extrapulmonary tuberculosis,,0050598,,,C0679362,,,,,,,,
mondo:0000369,abdominal tuberculosis,,0050599,,,C0740652,,,,,014.80,,,
mondo:0000371,oral cavity carcinoma in situ,"['carcinoma in situ of the mouth', 'stage 0 oral cavity cancer aJCC v6 and v7', 'carcinoma in situ of oral cavity', 'stage 0 oral cavity cancer aJCC v7', 'stage 0 mouth carcinoma', 'mouth carcinoma in situ', 'carcinoma in situ of mouth', 'stage 0 oral cavity cancer', 'stage 0 carcinoma of oral cavity', 'stage 0 carcinoma of the mouth', 'stage 0 carcinoma of the oral cavity', 'stage 0 oral cavity cancer aJCC v6', 'stage 0 carcinoma of mouth', 'stage 0 oral cavity carcinoma', 'carcinoma in situ of the oral cavity', 'oral cavity in situ carcinoma']",0050610,,,C0347073,,C4587,,,,,,
mondo:0000372,pharynx carcinoma in situ,"['stage 0 pharyngeal cancer', 'pharyngeal carcinoma in situ', 'stage 0 pharynx carcinoma', 'pharyngeal cancer stage 0', 'stage 0 carcinoma of pharynx', 'carcinoma in situ of pharynx', 'pharynx carcinoma in situ', 'carcinoma in situ of the pharynx', 'stage 0 pharyngeal carcinoma', 'pharynx in situ carcinoma', 'stage 0 carcinoma of the pharynx', 'stage 0 pharyngeal throat cancer']",0050611,,,C0347098,,C4942,,,,,,
mondo:0000373,gall bladder carcinoma in situ,"['carcinoma in situ of gall bladder', 'stage 0 gall bladder carcinoma', 'gall bladder in situ carcinoma']",0050612,,,,,,,,,,,
mondo:0000374,bile duct carcinoma in situ,"['bile duct in situ carcinoma', 'stage 0 bile duct carcinoma', 'carcinoma in situ of bile duct']",0050613,,,,,,,,,,,
mondo:0000375,bronchus carcinoma in situ,"['stage 0 bronchus carcinoma', 'bronchus in situ carcinoma', 'carcinoma in situ of bronchus']",0050614,,,C2939445,,,,,,,,
mondo:0000376,respiratory system cancer,"['cancer of respiratory system', 'respiratory system cancer', 'malignant respiratory system neoplasm', 'malignant neoplasm of respiratory system']",0050615,,,C3164456,,,,,165.9,,,
mondo:0000377,malignant Leydig cell tumor,"['cancer of Leydig cell', 'Leydig cell tumor, malignant', 'malignant Leydig cell neoplasm', 'malignant interstitial cell tumor', 'Leydig cell cancer', 'malignant interstitial cell neoplasm', 'malignant neoplasm of Leydig cell', 'malignant interstitial cell tumour']",0050616,,,C0334410,,C4213,,,,,,
mondo:0000378,malignant Sertoli cell tumor,"['malignant Androblastoma', 'Sertoli cell tumor, malignant']",0050617,,,C0334406,,C67006,,,,,,
mondo:0000379,malignant Sertoli-Leydig cell tumor,"['Sertoli-Leydig cell tumor, malignant']",0050618,,,,,,,,,,,
mondo:0000380,paranasal sinus carcinoma,"['carcinoma of accessory sinus', 'paranasal sinus cancer', 'adenoid cystic carcinoma of accessory sinus', 'paranasal sinus adenocarcinoma', 'epidermoid carcinoma of the paranasal sinus', 'adenoid cystic carcinoma of paranasal sinus', 'paranasal sinus carcinoma', 'squamous cell carcinoma of paranasal sinus', 'carcinoma of paranasal sinus', 'malignant paranasal sinus neoplasm', 'accessory sinus carcinoma', 'paranasal sinus squamous cell carcinoma', 'mucoepidermoid carcinoma of accessory sinus', 'paranasal sinus mucoepidermoid carcinoma', 'carcinoma of the paranasal sinus', 'malignant neoplasm of paranasal sinus', 'cancer of paranasal sinus', 'accessory sinus cancer', 'carcinoma of the accessory sinus', 'paranasal sinus adenoid cystic carcinoma']",0050619,,,C1335337,,C6019,,,,,,
mondo:0000381,infiltrating renal pelvis transitional cell carcinoma,,0050620,,,,,,,,,,,
mondo:0000382,respiratory system benign neoplasm,['respiratory system benign neoplasm'],0050621,,,C0497556,,,,,,,,
mondo:0000383,benign reproductive system neoplasm,"['reproductive organ benign neoplasm', 'benign reproductive system neoplasm']",0050622,,,C1332536,,C7617,,,,,,
mondo:0000384,bladder benign neoplasm,"['benign bladder tumour', 'benign neoplasm of urinary bladder', 'benign tumour of the urinary bladder', 'benign neoplasm of bladder', 'urinary bladder benign neoplasm', 'benign neoplasm of the bladder', 'benign tumour of urinary bladder', 'benign neoplasm of the urinary bladder', 'benign tumor of the urinary bladder', 'benign tumour of the bladder', 'benign bladder neoplasm', 'benign bladder tumor', 'benign tumour of bladder', 'benign urinary bladder tumor', 'benign urinary bladder neoplasm', 'benign tumor of urinary bladder', 'benign urinary bladder tumour', 'benign tumor of the bladder', 'benign tumor of bladder']",0050623,,,C0154017,,C3618,,,223.3,,,
mondo:0000385,benign digestive system neoplasm,"['alimentary part of gastrointestinal system benign neoplasm', 'benign tumor of the digestive system', 'benign tumour of GI system', 'benign tumor of digestive system', 'gastrointestinal system benign neoplasm', 'benign GI tumour', 'benign GI system neoplasm', 'benign tumour of the digestive system', 'benign GI neoplasm', 'benign neoplasm of the digestive system', 'benign digestive system tumour', 'benign GI system tumor', 'benign GI tumor', 'benign gastrointestinal neoplasm', 'benign gastrointestinal system tumour', 'benign gastrointestinal tumour', 'benign gastrointestinal system tumor', 'benign neoplasm of gastrointestinal system', 'benign tumor of GI system', 'benign tumor of the GI system', 'benign tumour of digestive system', 'benign tumour of gastrointestinal system', 'benign tumour of the GI system', 'benign GI system tumour', 'benign tumor of the gastrointestinal system', 'benign tumour of the gastrointestinal system', 'benign tumor of gastrointestinal system', 'benign neoplasm of digestive system', 'benign gastrointestinal tumor', 'benign digestive system tumor']",0050624,,,C0497538,,C4787,,,,,,
mondo:0000386,"digestive system neuroendocrine tumor, grade 1/2","['gastrointestinal neuroendocrine tumours', 'digestive system neuroendocrine tumor', 'digestive system well differentiated neuroendocrine tumour', 'gastrointestinal neuroendocrine tumour', 'gastrointestinal system neuroendocrine tumor', 'digestive system NET', 'digestive system well differentiated neuroendocrine tumor', 'digestive system neuroendocrine tumour', 'GINET', 'malignant gastrointestinal neuroendocrine tumor', 'gastrointestinal NET', 'malignant gastrointestinal neuroendocrine tumour', 'gastroenteropancreatic neuroendocrine tumour', 'gastrointestinal neuroendocrine tumors', 'gastroenteropancreatic NET', 'gastrointestinal neuroendocrine tumor', 'gastrointestinal system neuroendocrine tumour', 'gastroenteropancreatic neuroendocrine tumor', 'alimentary part of gastrointestinal system neuroendocrine tumor', 'alimentary part of gastrointestinal system neuroendocrine tumour']",0050626,,,C2987127,,C95404,,,,,,
mondo:0000387,hypochromic microcytic anemia,"['hypochromic microcytic anemia (disease)', 'hypochromic microcytic anemia', 'hypochromic microcytic anaemia (disease)']",0050642,,,C0271901,,,,C536357,,,,0004840
mondo:0000389,atelosteogenesis,,0050648,,,CN163181,,,,,,,,
mondo:0000390,vitelliform macular dystrophy,"['vitelliform macular dystrophy', 'macular dystrophy, vitelliform']",0050661,,,C0339510,,C118788,,D057826,,H35.5,,
mondo:0000393,partial fetal alcohol syndrome,,0050666,,,C3661483,,,,,,,,
mondo:0000395,alcohol-related birth defect,"['alcohol related birth defect', 'ARBD']",0050668,,,C3146244,,C92727,,,,,,
mondo:0000396,spastic cerebral palsy,['hypertonic cerebral palsy'],0050669,,,C0338596,,C116903,,,344.89,,,
mondo:0000397,ataxic cerebral palsy,,0050670,,,C0394005,,C97168,,,343.8,,,
mondo:0000400,mixed cerebral palsy,,0050673,,,C0751024,,C97177,,,343.8,,,
mondo:0000402,small cell carcinoma,"['small cell NEC', 'oat cell cancer', 'small cell carcinoma', 'small cell carcinoma (extrapulmonary)', 'oat cell carcinoma', 'intermediate cell small cell carcinoma', 'small cell carcinoma, intermediate cell', 'small cell carcinoma, intermediate cell (morphologic abnormality)', 'small cell neuroendocrine carcinoma', 'small cell car. (extrapulmonary)', 'small cell cancer', 'small cell carcinoma - intermediate cell']",0050685,,,C0334239,,C4099,0008524,D018288,,,,
mondo:0000405,anal canal cancer,"['anal canal cancer', 'malignant anal canal neoplasm', 'malignant neoplasm of anal canal', 'cancer of anal canal']",0050688,,,C0153445,,,,,154.2,,,
mondo:0000407,malignant pleural solitary fibrous tumor,"['pleural solitary fibrous tumor, malignant']",0050695,,,,,,,,,,,
mondo:0000408,fetal alcohol spectrum disorder,"['FASD', 'birth defects, alcohol-related', 'syndrome, fetal alcohol', 'partial foetal alcohol syndrome', 'foetal alcohol spectrum disorders', 'FAE (fetal alcohol effects)', 'syndrome, foetal alcohol', 'alcohol-related neurodevelopmental disorder (ARND) - type', 'fetal alcohol syndrome (FAS) - type', 'fetal alcohol syndrome', 'alcohol related neurodevelopmental disorder', 'alcohol-related birth defects', 'growth retardation, facial abnormalities, and central nervous system dysfunction', 'alcohol-related birth defects (ARBD) - type', 'fetal alcohol spectrum disorders', 'alcohol related birth defects', 'partial fetal alcohol syndrome', 'foetal alcohol syndrome (FAS) - type', 'foetal alcohol syndrome', 'FASDs', 'FAEs (fetal alcohol effects)']",0050696,,,CN200663,,C92780,,D063647,,,,
mondo:0000409,chorioamnionitis,"['inflammation of foetal membrane', 'intra-amniotic infection', 'foetal membrane inflammation', 'fetal membrane inflammation']",0050697,,,,,C26720,,D002821,,,,
mondo:0000410,funisitis,,0050698,,,C1275592,,C97077,,,658.80,,,
mondo:0000411,electroclinical syndrome,['electro-clinical syndrome'],0050701,,,,,,,,,,,
mondo:0000412,neonatal period electroclinical syndrome,,0050702,,,,,,,,,,,
mondo:0000413,infancy electroclinical syndrome,,0050703,,,,,,,,,,,
mondo:0000414,childhood electroclinical syndrome,"['paediatric electroclinical syndrome', 'electroclinical syndrome of childhood', 'pediatric electroclinical syndrome']",0050704,,,,,,,,,,,
mondo:0000415,adolescence-adult electroclinical syndrome,,0050705,,,,,,,,,,,
mondo:0000417,early onset absence epilepsy,,0050708,,,,,,,,,,,
mondo:0000421,inborn serine deficiency,"['rare inborn error of L-serine biosynthetic process', 'inborn error of L-serine biosynthetic process']",0050721,,,,,,,,,,,
mondo:0000424,inborn vitamin B12 deficiency,"['inborn vitamin B12 deficiency (disease)', 'hypocobalaminemia', 'cobalamin deficiency', 'rare inborn error of cobalamin metabolic process', 'inborn error of cobalamin metabolic process']",0050731,,,,,,0000734,,,,,
mondo:0000425,X-linked disease,"['genetic disease, X-linked', 'disease, X-linked genetic', 'genetic diseases, X-chromosome linked', 'X-linked genetic disease', 'genetic diseases, X linked', 'disease, X-linked', 'X-linked disease or disorder', 'diseases, X-linked genetic', 'X linked genetic diseases', 'X-linked genetic diseases', 'genetic diseases, X chromosome linked', 'disease or disorder, X-linked']",0050735,,,C2828000,,C85865,,D040181,799.89,,,
mondo:0000426,autosomal dominant disease,"['autosomal dominant disease or disorder', 'disease, autosomal dominant', 'disease or disorder, autosomal dominant']",0050736,,,C0265385,,,,,758.5,,,
mondo:0000428,Y-linked disease,"['disease, Y-linked genetic', 'Y-linked disease or disorder', 'disease, Y-linked', 'genetic disease, Y-linked', 'Y linked genetic diseases', 'Y-linked genetic diseases', 'genetic diseases, Y-chromosome linked', 'disease or disorder, Y-linked', 'diseases, Y-linked genetic', 'Y-linked genetic disease', 'genetic diseases, Y linked', 'genetic diseases, Y chromosome linked']",0050738,,,C1563751,,,,D050174,,,,
mondo:0000429,autosomal genetic disease,,0050739,,,C0265384,,,,,758.5,,,
mondo:0000430,mature T-cell and NK-cell non-Hodgkin lymphoma,"['mature T-cell non-Hodgkin^s lymphoma', 'mature T-and NK-cell lymphoma', 'peripheral T-cell lymphoma', 'NK-T cell lymphoma', 'mature T-cell and natural killer cell lymphoma', 'mature T-cell and NK-cell lymphoma', 'mature T-cell and NK-cell non-Hodgkin^s lymphoma', 'mature T-cell lymphoma', 'PTCL', 'mature T-cell and NK-cell non-Hodgkin lymphoma']",0050749,,,,,C3468,,D016411,,C84.4,,
mondo:0000432,lymphoplasmacytic lymphoma,"['lymphoplasmacytic lymphoma', 'lymphoma, lymphoplasmacytic, malignant', 'lymphoplasmacytoid lymphoma', 'lymphoplasmacytic lymphoma (Waldenstrom macroglobulinemia)', 'Immunocytoma, lymphoplasmacytic type', 'lymphoma, plasmacytic']",0050747,,,C0334633,,C3212,,,273.3,,,
mondo:0000437,cerebellar ataxia,"['spinocerebellar Degeneration', 'cerebellar Ataxias', 'rare ataxia', 'cerebellar dysmetria', 'ataxia syndrome', 'ataxias, cerebellar', 'cerebellar Dysmetrias', 'ataxia', 'ataxia, cerebellar']",0050753,,102002,C0087012,,C82341,,D002524,334.3,,,
mondo:0000440,metabolic acidosis,,0050758,,,,,,,,,,,
mondo:0000446,midface dysplasia,,0050767,,,,,,,,,,,
mondo:0000447,autosomal dominant polycystic liver disease,"['fibrocystic liver disease', 'congenital hepatic cyst', 'PCLD', 'congenital cystic liver disease', 'isolated polycystic liver disease', 'AD polycystic liver disease', 'polycystic liver disease', 'ADPLD', 'isolated congenital polycystic liver disease']",0050770,,2924,C0158683,"['0.3843', '-0.0671', '-0.04092', '-0.4038', '0.3936', '0.04852', '-0.3708', '-0.2598', '-0.3062', '0.803', '0.759', '0.406', '-0.03833', '0.4478', '-0.6694', '-0.4954', '0.1179', '0.1868', '-0.6733', '-0.4348', '-0.808', '-0.0825', '0.04523', '0.2625', '-0.2507', '-0.7295', '-0.265', '0.5093', '-0.11584', '-0.762', '0.4436', '0.0973', '0.362', '0.06793', '0.5864', '-0.1771', '-1.181', '0.10114', '0.5703', '-0.2228', '-0.1117', '0.179', '0.1133', '-0.3953', '0.0722', '-0.5977', '0.1116', '-0.323', '-0.07544', '0.04376', '-0.3271', '-0.102', '0.501', '-0.1843', '0.0757', '-0.223', '0.2251', '0.2637', '-0.862', '-0.37', '0.4426', '0.2776', '0.02138', '0.01114', '0.0348', '0.266', '0.3167', '0.469', '-0.4097', '0.0165', '-0.162', '0.2208', '0.5356', '-0.797', '0.6323', '0.4753', '0.417', '0.6016', '0.0892', '0.5923', '-0.5186', '-0.3206', '-0.4536', '-0.522', '0.4778', '0.1611', '0.4282', '-0.2822', '0.1064', '0.287', '0.6187', '0.1971', '-0.1841', '0.4377', '0.7236', '-0.007965', '-0.5933', '-0.8403', '-0.3796', '-0.07794']",C82833,,,751.62,Q44.6,10083939,0006557
mondo:0000448,paraganglioma,"['paraganglion tumor', 'tumor of paraganglion', 'neoplasm of the paraganglion', 'tumour of the paraganglion', 'Paraganglionic neoplasm', 'paraganglioma', 'neoplasm of paraganglion', 'paraganglion neoplasm', 'Paraganglionic tumour', 'paraganglion tumour', 'paragangliomas', 'chemodectoma', 'Paraganglionic tumor', 'tumor of the paraganglion', 'tumour of paraganglion']",0050773,,,C0030421,"['0.3801', '-0.0839', '-0.2197', '-0.0965', '0.123', '0.3997', '0.884', '0.3198', '-0.3843', '0.396', '0.01463', '-0.0886', '-0.47', '-0.03008', '0.1304', '0.0685', '-0.00912', '-0.4868', '-0.2947', '-0.3066', '-0.2505', '-0.1707', '-0.2693', '-0.563', '0.08624', '-0.2455', '-0.1854', '-0.00503', '-0.1722', '-0.05643', '0.545', '-0.325', '0.3115', '-1.033', '0.2722', '-0.1357', '-0.11127', '-0.3926', '0.4172', '-1.031', '0.691', '-0.3545', '0.2168', '-0.626', '0.891', '0.4446', '0.3337', '-0.2451', '0.2825', '0.5635', '0.486', '0.3174', '-0.2703', '-0.1214', '0.0924', '0.3672', '-0.3562', '0.4548', '-0.7153', '0.05927', '0.1073', '-0.11694', '0.224', '0.3928', '-0.2319', '0.5894', '0.2925', '0.7007', '-0.2401', '0.858', '-0.1632', '0.764', '0.3572', '-0.2168', '0.657', '0.1907', '-0.00511', '0.3398', '0.492', '-0.3132', '0.2278', '0.2827', '-0.2158', '0.4749', '-0.3093', '-0.7173', '0.6997', '-0.09155', '0.6836', '-0.1041', '0.00252', '0.2544', '-0.2737', '-0.3137', '0.6357', '0.10156', '-0.07806', '-0.3113', '-0.3389', '-0.04376']",C3308,1000453,D010235,239.7,,,
mondo:0000450,secondary progressive multiple sclerosis,"['secondary-progressive MS', 'SPMS']",0050783,,,C0751965,,,0008522,,,,,
mondo:0000451,primary progressive multiple sclerosis,"['PPMS', 'primary-progressive MS']",0050784,,,C0751964,,,0008520,,,,,
mondo:0000452,progressive relapsing multiple sclerosis,"['progressive-relapsing MS', 'PRMS']",0050785,,,C0393666,,,,,,,,
mondo:0000453,short QT syndrome,"['familial short QT syndrome', 'ventricular arrhythmia associated with short QT syndrome']",0050793,,51083,C2348199,"['0.3076', '0.3433', '-0.4048', '-0.0634', '-0.3384', '-0.5396', '0.8564', '1.017', '0.1989', '-0.336', '0.517', '-0.2878', '0.3926', '-0.04233', '-0.1404', '0.7056', '-0.533', '-0.0885', '0.015495', '-0.6826', '-0.02641', '0.427', '0.1243', '-0.171', '0.2764', '-0.443', '-0.0769', '0.3276', '-0.05444', '-0.1698', '1.171', '0.332', '0.7153', '-0.186', '-0.2051', '-0.588', '0.327', '-0.0941', '0.4565', '-0.3499', '0.3647', '-0.102', '0.912', '-0.4863', '0.1013', '0.12225', '-0.9326', '0.325', '-0.4465', '0.3833', '0.1091', '0.2224', '-0.575', '-0.2297', '-0.2255', '-0.1833', '-0.2737', '-0.0049', '0.1243', '-0.0468', '0.0657', '0.1571', '0.512', '-0.3245', '-0.1206', '0.2046', '0.3928', '0.345', '-0.2352', '0.3728', '0.007607', '0.2632', '0.1672', '-0.2378', '0.2122', '-0.02916', '-0.0866', '-0.1001', '-0.3953', '0.04858', '0.0778', '0.0738', '-0.0239', '0.05185', '0.1709', '0.1398', '0.1311', '0.02193', '-0.0678', '0.1555', '-0.1295', '-0.1627', '-0.001649', '-0.05865', '0.899', '0.2306', '0.872', '-0.587', '-0.731', '0.2031']",C71060,,C580439,426.89,,,
mondo:0000455,cone dystrophy,"['retinal cone dystrophy', 'cone dystrophy', 'stationary cone dystrophy', 'progressive cone dystrophy']",0050795,,1871,C0730290,"['-0.5454', '0.01639', '-0.04514', '0.02', '0.1576', '-0.3914', '-0.1349', '0.4236', '-0.2296', '-0.1996', '-0.0411', '-0.1664', '-0.284', '0.205', '-0.1691', '-0.5186', '0.3652', '-0.1141', '-0.12494', '-0.411', '-0.379', '-0.4536', '-0.1615', '0.349', '0.003569', '-0.004757', '-0.054', '-0.1958', '-0.3235', '0.4631', '0.509', '0.2732', '0.0772', '0.1992', '0.01765', '0.406', '0.04276', '-0.1517', '0.1747', '-0.2874', '0.3904', '-0.2578', '-0.1094', '0.04156', '-0.3813', '-0.02098', '-0.2195', '-0.2148', '0.1501', '0.2274', '0.305', '0.4055', '0.1182', '-0.2861', '0.12335', '-0.2129', '0.6484', '-0.08093', '-0.535', '0.0722', '0.2211', '-0.0857', '0.336', '0.2106', '-0.223', '-0.005104', '0.606', '0.726', '-0.1312', '0.405', '-0.04996', '-0.1873', '0.003437', '-0.1698', '0.622', '-0.07117', '0.1153', '0.135', '-0.2595', '-0.03812', '0.1964', '-0.326', '0.186', '0.2976', '-0.2482', '-0.3015', '-0.06934', '-0.01588', '0.244', '0.1488', '0.1854', '0.404', '-0.02283', '0.4395', '0.3655', '0.0982', '0.405', '-0.3384', '0.2017', '0.3484']",,,D000077765,362.75,,,
mondo:0000456,cerebral creatine deficiency syndrome,"['CCDS', 'CDS', 'cerebral creatine deficiency syndrome', 'creatine deficiency syndrome']",0050798,,79172,CN227588,,,,,,,,
mondo:0000457,classical glioblastoma,"['classical glioblastoma', 'glioblastoma classical subtype']",0050803,,,C3827253,,C111694,,,,,,
mondo:0000458,proneural glioblastoma,"['glioblastoma proneural subtype', 'proneural glioblastoma']",0050804,,,C3828464,,C111692,,,,,,
mondo:0000459,mesenchymal glioblastoma,"['mesenchymal glioblastoma', 'glioblastoma mesenchymal subtype']",0050805,,,C3829122,,C111695,,,,,,
mondo:0000460,neural glioblastoma,"['neural glioblastoma', 'glioblastoma neural subtype']",0050806,,,C3828832,,C111693,,,,,,
mondo:0000461,nutritional biotin deficiency,"['B7 deficiency', 'biotin deficiency']",0050810,,,,,,,C531633,,,,
mondo:0000462,eye adnexa disorder,"['disease of ocular adnexa', 'ocular adnexa disease', 'disorder of ocular adnexa', 'ocular adnexa disease or disorder']",0050815,,519266,C1290855,,,,,,,,
mondo:0000463,Ochoa syndrome,"['inverted smile-neurogenic bladder syndrome', 'urofacial Ochoa^s syndrome', 'UFS', 'partial facial palsy with urinary abnormalities', 'inverted smile and occult neuropathic bladder', 'urofacial syndrome', 'hydronephrosis with peculiar facial expression', 'Ochoa syndrome', 'hydronephrosis-inverted smile syndrome']",0050816,,2704,,"['0.2275', '0.02611', '-0.015335', '-0.1259', '-0.729', '-0.1375', '0.0798', '0.7007', '-0.1971', '-0.3735', '0.0668', '-0.09503', '-0.07965', '0.1288', '0.12195', '0.343', '-0.1417', '-0.10333', '-0.636', '-0.5664', '0.2333', '-0.05692', '-0.0333', '-0.4624', '0.265', '-0.3455', '-0.289', '0.2295', '0.3726', '-0.1556', '0.01994', '-0.279', '-0.03275', '-0.2817', '-0.1564', '-0.3', '0.137', '-0.1139', '0.2546', '-0.0311', '0.2808', '0.02142', '0.2751', '-0.2966', '0.2634', '0.1497', '-0.10956', '-0.2009', '-0.4822', '0.2205', '-0.6704', '0.5693', '-0.05463', '0.04745', '-0.2866', '0.2129', '0.1445', '-0.1614', '-0.2874', '0.6494', '0.3857', '0.486', '-0.0166', '0.4368', '0.284', '-0.1772', '0.5854', '0.1841', '-0.45', '0.5405', '-0.776', '0.3372', '0.0698', '0.0003538', '0.0887', '-0.01246', '0.1614', '-0.04837', '-0.4363', '-0.1196', '0.3333', '-0.3008', '0.2673', '0.641', '-0.0187', '0.617', '0.0838', '-0.06683', '0.3628', '-0.1908', '0.3801', '0.2413', '-0.369', '0.2705', '0.5327', '0.218', '-0.1204', '-0.5933', '0.775', '0.2231']",,,C536480,,,,
mondo:0000465,atrioventricular block,"['atrioventricular block (disease)', 'AV block', 'AV nodal block', 'atrioventricular block', 'AVB']",0050820,,,C0004245,,,,D054537,426.10,,,0001678
mondo:0000466,first-degree atrioventricular block,"['AV block first degree', 'first degree AV block', 'atrioventricular block first degree', 'atrioventricular block, first degree', 'first degree atrioventricular block']",0050821,,,C0085614,,C62015,,,426.11,,,
mondo:0000467,second-degree atrioventricular block,"['atrioventricular block, second degree', 'second degree atrioventricular block', 'atrioventricular block second degree', 'AV block second degree', 'second degree AV block', 'second-degree heart block']",0050822,,,C1621824,,C111119,,,426.13,,,
mondo:0000468,third-degree atrioventricular block,"['third degree AV block', 'third degree atrioventricular block', 'atrioventricular block complete', 'AV block third degree', 'non-congenital complete atrioventricular block', 'complete atrioventricular block', 'complete AV block', 'complete heart block', 'atrioventricular block, third degree']",0050823,,,C0151517,,C50501,,,426.0,,,
mondo:0000469,sinoatrial node disorder,"['disorder of sinoatrial node', 'sinuatrial node', 'SA node', 'disease of sinoatrial node', 'sinoatrial node disease', 'sinoatrial node disease or disorder']",0050824,,,,,,,,,,,
mondo:0000470,endocardium disorder,"['disorder of endocardium', 'endocardium disease', 'disease of endocardium', 'endocardium disease or disorder']",0050825,,,C0854140,,,,,,,,
mondo:0000471,tricuspid valve disorder,"['tricuspid disease', 'disease of tricuspid valve', 'rheumatic disease of tricuspid valve', 'tricuspid valve disease', 'tricuspid valve disease or disorder', 'RH. tricuspid valve disease', 'tricuspid valve disorder', 'disorder of tricuspid valve', 'rheumatic tricuspid valve disease']",0050826,,,C0264882,,C78649,,,397.0,,,
mondo:0000473,arterial disorder,"['arterial disorder', 'disease of artery', 'artery disease', 'disorder of artery', 'arteriopathy', 'arterial disease', 'artery disease or disorder']",0050828,,,C0852949,,C35317,,,447.9,,,
mondo:0000474,pericardium disorder,"['disease of pericardium', 'disorder of pericardium', 'pericardium disease or disorder', 'pericardium disease']",0050829,,,C0265122,,,,,423.9,,,
mondo:0000476,generalized dystonia,"['torsion disease of childhood', 'dystonia musculorum deformans', 'generalized isolated dystonia', 'torsion spasm, Progressive', 'symptomatic torsion dystonia', 'Progressive torsion spasm', 'torsion disease, childhood', 'dystonias, torsion', 'idiopathic familial dystonia', 'Oppenheim Ziehen disease', 'torsion dystonia, Idiopathic', 'spasm, Progressive torsion', 'dystonia, Idiopathic torsion', 'idiopathic torsion dystonia', 'dystonia deformans progressiva', 'Idiopathic torsion dystonia', 'generalised isolated dystonia', 'dystonia 12', 'dystonia deformans musculorum', 'childhood torsion disease', 'Idiopathic torsion dystonias', 'torsion dystonia', 'Oppenheim-Ziehen disease', 'familial dystonia', 'fragments of torsion dystonia', 'idiopathic non-familial dystonia', 'dystonias, Idiopathic torsion']",0050835,,376724,,,,,D004422,333.89,,,
mondo:0000477,focal dystonia,,0050836,,,C0743332,,,,,,,,
mondo:0000478,multifocal dystonia,,0050837,,,,,,,,,,,
mondo:0000479,segmental dystonia,,0050838,,,C1997740,,,,,333.89,,,
mondo:0000480,anismus,"['puborectalis syndrome', 'anal region skeletal muscle focal dystonia', 'dyskinetic puborectalis', 'focal dystonia of anal region skeletal muscle', 'dyssynergic defecation']",0050839,,,C0267601,,,,,569.49,,,
mondo:0000481,cervical dystonia,['spasmodic torticollis'],0050840,,93962,,"['0.341', '0.12415', '0.1002', '-0.3262', '-0.4192', '-0.7773', '0.678', '0.002396', '-1.0205', '-0.1393', '0.8296', '0.7246', '-0.2097', '0.2338', '0.5435', '0.582', '-0.1262', '-0.8657', '-0.6064', '-1.027', '-0.5283', '0.14', '-0.05737', '-0.3289', '-0.2085', '0.1112', '-0.1136', '0.1699', '-0.254', '0.1053', '0.2483', '0.378', '0.876', '-0.3093', '0.39', '-0.01236', '0.4048', '-0.2083', '0.3354', '-0.4822', '0.508', '-0.02199', '-0.2974', '0.1986', '0.606', '-0.1865', '-0.2416', '0.1969', '0.4343', '0.6436', '0.113', '0.0726', '0.434', '0.01246', '0.3586', '0.01024', '0.2874', '0.8745', '0.0625', '-0.126', '-0.614', '-0.4678', '-0.06683', '-0.5654', '-1.044', '0.504', '0.5317', '0.2242', '-0.2585', '0.4875', '-0.1176', '-0.0516', '-0.01255', '-0.199', '0.4568', '0.658', '0.5566', '-0.0783', '-0.2717', '-0.3503', '-0.1896', '0.131', '0.4062', '0.3752', '0.7866', '0.007492', '0.1846', '0.649', '1.299', '0.2505', '-0.05728', '-0.01901', '0.5513', '0.275', '0.7305', '-0.06012', '-0.417', '0.05338', '0.1421', '-0.533']",C85072,,,333.83,,,
mondo:0000482,focal hand dystonia,"['hand and arm dystonia', 'writer^s cramp', 'organic writer^s cramp']",0050841,,,C0154676,,,,,333.84,,,
mondo:0000483,oculogyric crisis,,0050842,,,,,,,,,,,
mondo:0000485,spasmodic dystonia,"['spastic dysphonia', 'spasmodic dysphonia', 'abductor spasmodic dysphonia', 'mixed spasmodic dysphonia (type)', 'laryngeal dystonia', 'laryngeal dyskinesia', 'adductor spasmodic dysphonia']",0050844,,93961,C1963946,,,,D055154,478.79,,,
mondo:0000486,craniofacial dystonia,['cranio-facial dystonia'],0050845,,,C4023011,,,,,,,,
mondo:0000487,hemidystonia,,0050846,,,C1960561,,,,,333.99,,,
mondo:0000488,periampullary adenoma,['periampullary region of duodenum adenoma'],0050849,,,CN068444,,,,,,,,
mondo:0000489,diabetic encephalopathy,,0050850,,,,,,,,,,,
mondo:0000490,glomerulosclerosis,['glomerular sclerosis'],0050851,,,C0178664,,C120888,,,,,,
mondo:0000491,limb ischemia,"['limb ischemic disease', 'ischaemic disease of limb', 'limb ischaemic disease', 'limb ischemia', 'ischemic disease of limb']",0050852,,,C2945695,,,,,,,,
mondo:0000492,chronic venous insufficiency,"['venous insufficiency (disease), chronic']",0050853,,,C1306557,,,0007940,,,,,
mondo:0000494,renal fibrosis,,0050855,,,C0151650,,,1001517,,,,,
mondo:0000495,oppositional defiant disorder,"['oppositional defiant disorder', 'oppositional defiant disorder (disease)']",0050856,,,,,C92565,,D019958,313.81,,,0010865
mondo:0000496,hemorrhagic cystitis,,0050859,,,C0085692,,C114666,,,,,,
mondo:0000497,pyometritis,"['myometrium inflammation', 'pyometra']",0050862,,,C0686163,,C121207,,D055112,,,,
mondo:0000498,arteritic anterior ischemic optic neuropathy,['arteritic aion'],0050863,,,C2242711,,,,,,,,
mondo:0000499,non-arteritic anterior ischemic optic neuropathy,"['nonarteritic anterior ischaemic optic neuropathy', 'non-arteritic aion', 'NAION', 'nonarteritic anterior ischemic optic neuropathy']",0050864,,415300,C1852242,,,,,,,,
mondo:0000500,tongue squamous cell carcinoma,"['scc of the tongue', 'tongue squamous cell carcinoma', 'scc of tongue', 'tongue scc', 'squamous cell carcinoma of tongue', 'squamous cell carcinoma of the tongue']",0050865,,,C0349566,,C4648,1000055,,,,,
mondo:0000502,villous adenoma,['villous adenoma'],0050869,,,C0206674,,C7399,,D018253,,,,
mondo:0000503,lung adenocarcinoma in situ,"['in situ pulmonary adenocarcinoma', 'adenosquamous cell carcinoma in situ of lung', 'stage 0 adenosquamous cell lung carcinoma', 'bronchioalveolar carcinoma', 'stage 0 adenosquamous lung carcinoma aJCC v6', 'bronchioloalveolar carcinoma', 'stage 0 adenosquamous cell carcinoma of the lung', 'stage 0 adenosquamous lung carcinoma aJCC v7', 'stage 0 adenosquamous cell carcinoma of lung', 'stage 0 adenosquamous lung carcinoma aJCC v6 and v7', 'adenosquamous cell carcinoma in situ of the lung', 'lung adenocarcinoma In situ', 'lung adenosquamous cell carcinoma in situ', 'stage 0 adenosquamous lung cancer']",0050870,,,C0854971,,C8748,,,,,,
mondo:0000507,inclusion body myopathy with Paget disease of bone and frontotemporal dementia,"['pagetoid amyotrophic lateral sclerosis', 'inclusion body myopathy/Paget disease/frontotemporal dementia', 'pagetoid neuroskeletal syndrome', 'IBMPFD', 'limb-girdle muscular dystrophy with Paget disease of bone', 'inclusion body myopathy with Paget^s disease of bone and frontotemporal dementia', 'inclusion body myopathy with early-onset Paget disease and frontotemporal dementia']",0050881,,52430,C1833662,"['0.1233', '-0.1073', '0.02135', '-0.3088', '-0.285', '-0.4338', '0.04984', '0.3198', '-0.7603', '-0.3274', '0.097', '-0.409', '0.0246', '0.7754', '0.268', '-0.7163', '-0.1941', '-0.322', '-0.543', '-0.04358', '0.2888', '-0.1357', '-0.2062', '-0.00426', '0.7124', '-0.4136', '0.02434', '0.1043', '-0.2734', '-0.2456', '0.0609', '-0.188', '-0.0799', '-0.59', '0.6177', '-0.3616', '-0.3591', '-0.3323', '0.3694', '-1.225', '0.4978', '-0.4329', '0.2194', '-0.1649', '-0.005905', '-0.1008', '0.4368', '-0.2051', '0.2847', '0.421', '0.1503', '0.0349', '0.4185', '-0.3435', '0.1404', '0.0844', '-0.01886', '-0.587', '-0.5034', '-0.646', '-0.0791', '0.2335', '0.3154', '-0.871', '0.02638', '0.7207', '0.33', '0.963', '-0.8164', '0.4607', '0.4116', '-0.1686', '0.1044', '-0.09125', '-0.2234', '0.744', '-0.04355', '0.179', '-0.682', '-0.07764', '-0.2686', '-0.637', '-0.4114', '0.835', '0.4985', '0.6055', '-0.1748', '-0.1122', '1.434', '0.648', '0.2411', '0.41', '0.04355', '0.7666', '-0.6357', '0.3796', '-0.2495', '0.04547', '-0.527', '-0.6113']",,,,,,,
mondo:0000508,syndromic intellectual disability,"['syndrome associated with intellectual disability', 'syndromic intellectual disability']",0050888,,,CN225415,"['-0.03622', '0.04465', '0.03214', '-0.05054', '0.03616', '-0.1052', '0.01826', '0.1046', '-0.06726', '-0.057', '-0.01915', '-0.01336', '0.003836', '0.0009623', '-0.02467', '-0.02188', '0.006683', '-0.01762', '-0.0509', '-0.1841', '0.01356', '0.00814', '0.03958', '-0.02101', '0.0573', '-0.04843', '-0.009926', '-0.013054', '0.0197', '-0.05362', '0.0584', '-0.00918', '0.1109', '0.05847', '0.01826', '-0.03577', '-0.03485', '-0.0449', '-0.02454', '-0.0694', '0.04825', '-0.0746', '-0.000916', '-0.03482', '-0.01227', '-0.09204', '-0.00681', '0.04337', '0.003271', '0.01593', '-0.04633', '0.000655', '0.00828', '-0.01907', '-0.0161', '0.01892', '0.0242', '-0.02277', '-0.0685', '0.0334', '0.03256', '0.0002565', '0.02126', '0.00697', '-0.007088', '0.03296', '0.02875', '0.1095', '-0.081', '0.06555', '-0.0652', '0.02895', '0.02045', '-0.05215', '0.03247', '0.04547', '0.05283', '-0.02315', '-0.04462', '-0.03735', '-0.01198', '0.01494', '-0.06094', '0.11835', '0.00946', '0.03082', '0.003674', '0.0602', '0.0778', '0.06274', '0.0346', '0.11487', '-0.011024', '0.02924', '0.1523', '0.04596', '0.0415', '-0.06934', '0.05453', '0.04932']",,,,,,,
mondo:0000509,non-syndromic intellectual disability,"['isolated intellectual disability', 'nonsyndromic intellectual disability']",0050889,,,,,,,,,,,
mondo:0000510,synucleinopathy,"['alpha synucleinopathies', 'synucleinopathies']",0050890,,,C5191670,,,,D000080874,,,,
mondo:0000513,bone ameloblastoma,"['ameloblastoma of bone tissue', 'bone tissue ameloblastoma']",0050895,,,,,,,,,,,
mondo:0000514,bone squamous cell carcinoma,['bone tissue squamous cell carcinoma'],0050896,,,,,,,,,,,
mondo:0000515,bone chondrosarcoma,['bone tissue chondrosarcoma (disease)'],0050897,,,,,,,,,,,
mondo:0000516,phalanx chondroma,['phalanx chondroma'],0050898,,,,,,,,,,,
mondo:0000517,brain stem medulloblastoma,"['brainstem medulloblastoma', 'medulloblastoma of brainstem']",0050899,,,,,,,,,,,
mondo:0000518,sacrum chordoma,['fused sacrum chordoma (disease)'],0050900,,,C3164279,,,,,,,,
mondo:0000519,corpus callosum oligodendroglioma,"['corpus callosum oligodendroglioma', 'oligodendroglioma of corpus callosum']",0050901,,,,,,,,,,,
mondo:0000520,parietal lobe ependymal tumor,"['ependymal tumor of parietal lobe', 'parietal lobe ependymal tumor', 'ependymal tumour of parietal lobe', 'parietal lobe ependymoma']",0050903,,,C4330935,,C131575,,,,,,
mondo:0000521,salivary gland carcinoma,"['carcinoma of salivary gland', 'salivary carcinoma', 'carcinoma of saliva-secreting gland', 'salivary gland cancer', 'salivary gland carcinoma', 'carcinoma of the salivary gland', 'saliva-secreting gland carcinoma']",0050904,,,C0948750,,C9272,,,,,,
mondo:0000524,mixed extragonadal germ cell cancer,,0050907,,,,,,,,,,,
mondo:0000525,cecum villous adenoma,"['cecum adenoma', 'caecum villous adenoma', 'cecum villous adenoma', 'villous adenoma of the cecum', 'cecal villous adenoma', 'caecum adenoma', 'villous adenoma of cecum']",0050910,,,C1332869,,C5520,1000155,,,,,
mondo:0000527,colon adenoma,"['colon adenoma', 'adenoma of the colon', 'colonic adenoma', 'adenoma of colon']",0050912,,,C0850572,,C3864,,,,,,
mondo:0000530,rectum adenoma,"['adenoma of the rectum', 'rectal adenoma', 'rectum adenoma', 'adenoma of rectum']",0050915,,,C1302652,,C5546,,,,,,
mondo:0000531,bronchus mucoepidermoid carcinoma,['bronchus mucoepidermoid carcinoma'],0050916,,,,,,,,,,,
mondo:0000532,lung combined type small cell adenocarcinoma,,0050917,,,,,,,,,,,
mondo:0000534,trachea mucoepidermoid carcinoma,['trachea mucoepidermoid carcinoma'],0050919,,,C3873401,,,,,,,,
mondo:0000535,tonsil squamous cell carcinoma,['tonsil squamous cell carcinoma'],0050920,,,,,,,,,,,
mondo:0000536,pharyngeal squamous cell carcinoma,"['pharyngeal squamous cell carcinoma', 'pharyngeal throat squamous cell cancer', 'pharyngeal squam. cell carcinoma', 'pharynx squamous cell carcinoma', 'pharyngeal (including hypopharyngeal and oropharyngeal) squamous cell carcinoma']",0050921,,,C1319317,,C102872,1001965,,,,,
mondo:0000539,striated muscle rhabdoid tumor,"['striated muscle tissue rhabdoid tumor', 'striated muscle tissue rhabdoid tumour']",0050924,,,,,,,,,,,
mondo:0000540,small intestinal neuroendocrine tumor G1,"['small intestinal carcinoid tumour', 'small intestine neuroendocrine tumor, well differentiated, low grade', 'small intestinal neuroendocrine tumor G1', 'small intestine carcinoid tumor (disease)', 'carcinoid tumour of the small bowel', 'carcinoid tumour of the small intestine', 'small intestine carcinoid tumour (disease)', 'carcinoid tumor of the small intestine', 'small intestine carcinoid tumor', 'carcinoid tumor of the small bowel', 'grade 1 neuroendocrine neoplasm of small intestine', 'carcinoid tumor of small bowel', 'small intestinal carcinoid tumor', 'small bowel carcinoid tumour', 'small intestine NET G1', 'carcinoid tumour of small bowel', 'small bowel carcinoid tumor', 'carcinoid tumour of small intestine', 'small intestine carcinoid neuroendocrine tumour', 'carcinoid tumor of small intestine', 'small intestine carcinoid neuroendocrine tumor', 'small intestinal NET G1', 'small intestine carcinoid tumour']",0050925,,,C0349536,,C4638,,,,,,
mondo:0000541,jejunal adenocarcinoma,"['jejunal adenocarcinoma (disease)', 'jejunum adenocarcinoma', 'jejunal adenocarcinoma']",0050926,,,C4072935,,C181158,,,,,,0030411
mondo:0000543,ovarian melanoma,"['ovary melanoma (disease)', 'ovary metastatic melanoma']",0050928,,,,,C178441,,,,,,
mondo:0000544,mucosal melanoma,['mucosal melanoma'],0050929,,,C3898222,,C114828,,,,,,
mondo:0000545,sublingual gland adenoid cystic carcinoma,['sublingual gland adenoid cystic carcinoma'],0050930,,,,,,,,,,,
mondo:0000548,ovarian clear cell cancer,"['ovarian clear cell carcinoma', 'malignant ovarian clear cell tumor', 'clear-cell ovarian carcinoma', 'malignant ovarian clear cell neoplasm', 'malignant ovarian clear cell tumour']",0050934,,,C1518230,,C40077,,,,,,
mondo:0000549,cervical neuroblastoma,"['neuroblastoma of neck', 'neck neuroblastoma']",0050935,,,,,,,,,,,
mondo:0000550,extra-adrenal sympathetic paraganglioma,"['extraadrenal pheochromocytoma', 'extra-adrenal pheochromocytoma', 'extra-adrenal chromaffin neoplasm', 'extra-adrenal sympathetic Paraganglionic neoplasm', 'extra-adrenal Chromaffinoma', 'extra-adrenal sympathetic paraganglioma']",0050936,,,C1257877,,C48576,0000489,,,,,
mondo:0000551,retroperitoneal neuroblastoma,['retroperitoneal space neuroblastoma'],0050937,,,,,,,,,,,
mondo:0000552,breast lobular carcinoma,"['lobular breast carcinoma', 'lobule of mammary gland carcinoma', 'lobular carcinoma', 'carcinoma of lobule of mammary gland', 'lobular carcinoma of breast', 'lobular carcinoma of the breast', 'lobular adenocarcinoma']",0050938,,,,,C3771,0008509,,,,,
mondo:0000553,uterine corpus endometrial carcinoma,['body of uterus endometrial carcinoma (disease)'],0050939,,,,,,,,,,,
mondo:0000554,endocervical adenocarcinoma,"['endocervix adenocarcinoma', 'endocervical adenocarcinoma, usual type']",0050940,,,C4289591,,C127907,,,,,,
mondo:0000563,GRID2-related autosomal dominant spinocerebellar ataxia,['GRID2-related spinocerebellar ataxia'],0050988,,,,,,,,,,,
mondo:0000565,infective endocarditis,"['endocarditis infective', 'endocarditis, infective']",0060000,,570762,,,C78265,,,136.9,,,
mondo:0000568,autoimmune disorder of central nervous system,"['central nervous system autoimmune disease', 'central nervous system hypersensitivity reaction type II disease']",0060004,,,,,,,,,,,
mondo:0000569,autoimmune disorder of endocrine system,"['endocrine system autoimmune disease', 'endocrine system hypersensitivity reaction type II disease']",0060005,,,C0342552,,,,,279.49,,,
mondo:0000572,recombinase activating gene 1 deficiency,,0060011,,,,,,,,,,,
mondo:0000573,recombinase activating gene 2 deficiency,,0060012,,,,,,,,,,,
mondo:0000577,congenital anemia,"['congenital anemia', 'congenital anemia (disease)', 'congenital anaemia (disease)']",,,,C0158995,,C35228,,,,,,
mondo:0000583,immunoglobulin beta deficiency,['IgB deficiency'],0060026,,,C3502055,,,,C567200,,,,
mondo:0000584,B cell linker protein deficiency,"['BLNK deficiency', 'B-cell linker protein deficiency']",0060027,,,,,,,,,,,
mondo:0000586,autoimmune disorder of exocrine system,"['exocrine system hypersensitivity reaction type II disease', 'exocrine system autoimmune disease']",0060029,,,,,,,,,,,
mondo:0000587,"autoimmune disease of ear, nose and throat","['autoimmune otorhinolaryngologic disease', 'autoimmune disease of eyes, ear, nose and throat']",0060030,,,,,,,,,,,
mondo:0000588,autoimmune disorder of gastrointestinal tract,"['autoimmune disease of alimentary part of gastrointestinal system', 'alimentary part of gastrointestinal system hypersensitivity reaction type II disease', 'alimentary part of gastrointestinal system autoimmune disease']",0060031,,,,,,,,,,,
mondo:0000589,autoimmune disorder of musculoskeletal system,"['musculoskeletal system autoimmune disease', 'musculoskeletal system hypersensitivity reaction type II disease']",0060032,,,,,,,,,,,
mondo:0000590,autoimmune disorder of peripheral nervous system,"['peripheral nervous system autoimmune disease', 'peripheral nervous system hypersensitivity reaction type II disease']",0060033,,,,,,,,,,,
mondo:0000591,intrinsic cardiomyopathy,['primary cardiomyopathy'],0060036,,,,,,,,,,,
mondo:0000592,specific developmental disorder,,0060038,,,,,,,,315.8,,,
mondo:0000594,pervasive developmental disorder,"['pervasive development disorder', 'pervasive child development disorders', 'pervasive development disorders']",0060040,,,,,C97179,,D002659,299.80,,,
mondo:0000595,sexual and gender identity disorders,['sexual disorder'],0060043,,,,,C92202,,,,,,
mondo:0000596,paraphilic disorder,"['paraphilia', 'Deviations, Sex', 'deviation, Sex', 'Paraphilias', 'paraphilic disorder', 'Sex Deviations', 'disorder, Paraphilic', 'paraphilia disorder', 'Sex deviation', 'disorders, Paraphilic']",0060044,,,,,,,D010262,,,,
mondo:0000597,Munchausen by proxy,"['Munchausen syndrome by proxy', 'Munchausen by proxy syndrome']",0060045,,,,,,,D016735,,,,
mondo:0000598,aphasia,,0060046,,,,,,,D001037,,R47.01,,
mondo:0000599,writing disorder,,0060047,,,,,,,,,,,
mondo:0000600,nosophobia,,0060048,,,,,,1001903,,,,,
mondo:0000602,autoimmune disorder of blood,"['blood autoimmune disease', 'blood hypersensitivity reaction type II disease']",0060050,,,,,,,,,,,
mondo:0000603,autoimmune disorder of cardiovascular system,"['cardiovascular system hypersensitivity reaction type II disease', 'cardiovascular system autoimmune disease']",0060051,,,,,,,,,,,
mondo:0000605,hypersensitivity reaction disease,"['hypersensitivity reaction', 'hypersensitive', 'allergic reaction', 'hypersensitivity', 'sensitivity', 'sensitive']",0060056,,,,,C3114,1002003,,,,,
mondo:0000607,primary cutaneous T-cell non-Hodgkin lymphoma,"['primary cutaneous T-cell non-Hodgkin^s lymphoma', 'CTCL', 'PCTCL', 'primary cutaneous T-cell non-Hodgkin lymphoma', 'cutaneous T-cell non-Hodgkin^s lymphoma', 'T-cell non-Hodgkin^s lymphoma of skin', 'T-cell non-Hodgkin^s lymphoma of the skin', 'cutaneous T-cell non-Hodgkin lymphoma', 'cutaneous T cell lymphoma', 'skin T-cell non-Hodgkin^s lymphoma', 'cutaneous T-cell lymphoma']",0060061,,,,,C3467,0002913,D016410,,,,
mondo:0000608,familial juvenile hyperuricemic nephropathy,"['familial juvenile hyperuricemic nephropathy', 'nephropathy, familial, with gout', 'tubulointerstitial kidney disease', 'FJHN', 'juvenile gout', 'familial nephropathy associated with hyperuricemia', 'gouty nephropathy, familial juvenile', 'familial juvenile gouty nephropathy', 'familial nephropathy with gout', 'juvenile gouty nephropathy', 'gouty nephropathy, familial']",0060062,,,CN239392,,,,C537696,,,,
mondo:0000610,marantic endocarditis,"['nonbacterial thrombotic endocarditis', 'non-bacterial thrombotic endocarditis']",0060068,,,,,,,D059905,,,,
mondo:0000611,pre-malignant neoplasm,,0060071,,,,,,,,,,,
mondo:0000612,lymphatic system cancer,"['malignant lymphatic part of lymphoid system neoplasm', 'lymphatic part of lymphoid system cancer', 'cancer of lymphatic part of lymphoid system', 'malignant neoplasm of lymphatic part of lymphoid system']",0060073,,,,,,,,,,,
mondo:0000615,progesterone-receptor positive breast cancer,,0060077,,,,,,,,,,,
mondo:0000616,progesterone-receptor negative breast cancer,,0060078,,,,,,,,,,,
mondo:0000618,Her2-receptor negative breast cancer,,0060080,,,C4733095,,C168519,0009780,,,,,
mondo:0000620,breast benign neoplasm,"['benign tumor of the breast', 'benign tumour of breast', 'benign tumour of the breast', 'benign neoplasm of the breast', 'benign tumor of breast', 'benign breast neoplasm', 'benign neoplasm of breast', 'benign breast tumour', 'breast benign neoplasm', 'benign breast tumor']",0060082,,,,,C4505,,,217,,,
mondo:0000621,immune system cancer,"['cancer of immune system', 'malignant immune system neoplasm', 'malignant neoplasm of immune system', 'immune system cancer']",0060083,,,,,,,,,,,
mondo:0000624,benign female reproductive system neoplasm,"['benign female reproductive system tumor', 'benign female reproductive system neoplasm', 'female reproductive organ benign neoplasm', 'benign gynecologic tumour', 'benign female reproductive system tumour', 'benign gynecologic tumor', 'benign gynecologic neoplasm']",0060086,,,C0744514,,C4934,,,,,,
mondo:0000625,benign male reproductive system neoplasm,"['male reproductive organ benign neoplasm', 'benign Male reproductive system neoplasm', 'benign Male reproductive system tumor', 'benign Male reproductive system tumour']",0060087,,,C0947786,,C4777,,,,,,
mondo:0000626,vestibular gland benign neoplasm,['vestibular gland benign neoplasm'],0060088,,,,,,,,,,,
mondo:0000627,benign endocrine neoplasm,"['benign neoplasm of the endocrine gland', 'benign neoplasm of endocrine gland', 'benign tumour of endocrine gland', 'benign tumour of the endocrine gland', 'benign endocrine gland neoplasm', 'endocrine organ benign neoplasm', 'benign endocrine neoplasm', 'benign endocrine gland tumour', 'benign endocrine gland tumor', 'benign endocrine tumor', 'benign endocrine tumour', 'benign tumor of the endocrine gland', 'benign tumor of endocrine gland', 'endocrine gland benign neoplasm']",0060089,,,C0347524,,C4621,,,227.9,,,
mondo:0000628,central nervous system organ benign neoplasm,['central nervous system benign neoplasm'],0060090,,,,,,,,,,,
mondo:0000629,cardiovascular organ benign neoplasm,['cardiovascular system benign neoplasm'],0060091,,,,,,,,,,,
mondo:0000630,immune system organ benign neoplasm,['immune organ benign neoplasm'],0060092,,,,,,,,,,,
mondo:0000631,bone benign neoplasm,"['benign osseous tumor', 'benign tumour of the bone', 'benign tumor of bone', 'benign neoplasm of bone', 'bone tissue benign neoplasm', 'benign tumour of bone', 'benign osseous tumour', 'benign bone neoplasm', 'benign bone tumor', 'benign bone tumour', 'benign tumor of the bone', 'benign osseous neoplasm', 'benign neoplasm of the bone']",0060094,,,,,C4880,,,213.9,,,
mondo:0000632,uterine benign neoplasm,"['benign uterus tumor', 'benign neoplasm of uterus', 'benign neoplasm of the uterus', 'uterine tumors, benign', 'Uterous neoplasms, benign', 'benign tumour of uterus', 'benign tumor of uterus', 'benign tumor of the uterus', 'benign tumour of the uterus', 'uterus benign neoplasm', 'benign uterus tumour', 'benign uterus tumours', 'benign uterine neoplasms', 'benign uterus neoplasm', 'Uterous tumors, benign', 'uterine neoplasms, benign', 'benign uterine tumour', 'benign uterine neoplasm', 'benign uterus tumors', 'benign uterine tumours', 'benign uterine tumor', 'benign uterus neoplasms', 'benign uterine tumors']",0060095,,,C0153999,,C3609,,,219.9,,,
mondo:0000633,sensory organ benign neoplasm,['sense organ benign neoplasm'],0060096,,,,,,,,,,,
mondo:0000634,thoracic benign neoplasm,"['benign thoracic neoplasm', 'benign tumor of thorax', 'benign neoplasm of the thorax', 'benign neoplasm of thorax', 'thoracic segment of trunk benign neoplasm', 'benign tumour of thorax', 'benign thoracic tumour', 'benign tumor of the thorax', 'benign tumour of the thorax', 'benign thoracic tumor']",0060097,,,C0346440,,C4565,,,229.8,,,
mondo:0000636,musculoskeletal system benign neoplasm,['musculoskeletal system benign neoplasm'],0060099,,,,,,,,,,,
mondo:0000637,musculoskeletal system cancer,"['malignant musculoskeletal system neoplasm', 'skeletal system cancer', 'cancer of musculoskeletal system', 'musculoskeletal system cancer', 'malignant neoplasm of musculoskeletal system']",0060100,,,,,,,,,,,
mondo:0000638,benign glioma,"['glioma, benign']",0060101,,,,,,,,,,,
mondo:0000639,cartilage cancer,"['cancer of cartilage tissue', 'cartilaginous cancer', 'malignant cartilage tissue neoplasm', 'cartilage tissue cancer', 'malignant neoplasm of cartilage tissue']",0060102,,,,,,,,,,,
mondo:0000640,central nervous system primitive neuroectodermal neoplasm,"['central nervous system PNET', 'CNS primitive neuroectodermal tumor', 'central nervous system neuroectodermal tumor', 'central nervous system primitive neuroectodermal neoplasm', 'central nervous system neuroectodermal tumour', 'CNS primitive neuroectodermal neoplasm', 'central primitive neuroectodermal neoplasm', 'central primitive neuroectodermal tumor', 'central nervous system primitive neuroectodermal tumor (WHO grade IV)', 'primitive neuroectodermal tumour of central nervous system', 'central nervous system primitive neuroectodermal tumour', 'CNS primitive neuroectodermal tumour', 'central nervous system primitive neuroectodermal tumour (WHO grade IV)', 'central nervous system primitive neuroectodermal tumor', 'primitive neuroectodermal tumor of central nervous system', 'central primitive neuroectodermal tumour', 'CNS PNET']",0060103,,,CN201960,,C5398,,,,,,
mondo:0000642,brain meningioma,['brain meningioma (disease)'],0060106,,,,,,,,,,,
mondo:0000643,vulvar benign neoplasm,"['benign vulva neoplasm', 'benign vulvar neoplasm', 'vulva benign neoplasm', 'benign tumour of vulva', 'benign vulvar tumor', 'benign vulva tumor', 'benign neoplasm of vulva', 'benign tumor of vulva', 'benign neoplasm of the vulva', 'benign tumour of the vulva', 'benign vulval neoplasm', 'benign tumor of the vulva', 'benign vulvar tumour', 'benign vulva tumour', 'mammalian vulva benign neoplasm']",0060109,,,C0154003,,C3611,,,,,,
mondo:0000644,cervical benign neoplasm,"['benign uterine cervix tumor', 'benign tumour of the uterine cervix', 'benign uterine cervix neoplasm', 'benign uterine cervix tumour', 'benign tumor of cervix uteri', 'benign neoplasm of uterine cervix', 'benign cervix uteri tumour', 'benign cervical neoplasm', 'benign cervix uteri tumor', 'benign tumor of the uterine cervix', 'benign neoplasm of the cervix uteri', 'uterine cervix benign neoplasm', 'benign tumor of the cervix uteri', 'benign tumour of cervix uteri', 'benign tumour of uterine cervix', 'benign tumor of uterine cervix', 'benign cervix uteri neoplasm', 'benign neoplasm of the uterine cervix', 'benign neoplasm of cervix uteri', 'benign tumour of the cervix uteri']",0060110,,,C0153997,,C3607,,,,,,
mondo:0000645,fallopian tube benign neoplasm,"['benign tumor of fallopian tube', 'benign tumour of fallopian tube', 'benign neoplasm of fallopian tube', 'fallopian tube tumor, benign', 'benign tumour of fallopian tubes', 'benign fallopian tube tumour', 'benign tumor of the fallopian tube', 'benign tumor of fallopian tubes', 'fallopian tube neoplasm, benign', 'benign neoplasm of the fallopian tube', 'benign fallopian tube tumor', 'benign tumour of the fallopian tube', 'fallopian tube benign neoplasm', 'benign fallopian tube neoplasm']",0060111,,180237,C0346190,,C4517,,,,,10053865,
mondo:0000646,ovarian benign neoplasm,"['ovary benign neoplasm', 'benign tumour of ovary', 'benign tumor of ovary', 'benign neoplasm of the ovary', 'benign tumor of the ovary', 'benign ovarian neoplasm', 'benign tumour of the ovary', 'benign ovarian tumor', 'benign ovarian tumour', 'benign neoplasm of ovary']",0060112,,,,,C2895,1000116,,,,,
mondo:0000647,benign vaginal neoplasm,"['benign vaginal neoplasms', 'benign tumor of the vagina', 'benign neoplasm of vagina', 'benign tumor of vagina', 'benign vaginal tumor', 'benign neoplasm of the vagina', 'vagina female reproductive organ benign neoplasm', 'benign vaginal tumour', 'vagina benign neoplasm', 'vaginal benign neoplasm', 'benign vaginal neoplasm', 'benign tumour of vagina', 'benign tumour of the vagina']",0060114,,,C0154002,,C3610,,,221.1,,,
mondo:0000648,nervous system benign neoplasm,"['benign tumour of nervous system', 'benign nervous system neoplasm', 'benign neoplasm of the nervous system', 'benign nervous system tumour', 'benign tumor of the nervous system', 'benign tumour of the nervous system', 'benign nervous system tumor', 'benign neoplasm of nervous system', 'benign tumor of nervous system', 'nervous system neoplasm, benign', 'nervous system benign neoplasm']",0060115,,,C0497550,,C4789,,,225.9,,,
mondo:0000649,sensory system cancer,"['malignant sensory system neoplasm', 'malignant neoplasm of sensory system', 'cancer of sensory system', 'sensory system cancer']",0060116,,,,,,,,,,,
mondo:0000650,peritoneal benign neoplasm,"['benign peritoneal neoplasm', 'peritoneum benign neoplasm']",0060117,,,C0496874,,C8612,,,,,,
mondo:0000652,integumentary system benign neoplasm,['integumental system benign neoplasm'],0060121,,,,,,,,,,,
mondo:0000653,integumentary system cancer,"['malignant neoplasm of integumental system', 'malignant integumental system neoplasm', 'integumental system cancer', 'cancer of integumental system']",0060122,,,,,,,,,,,
mondo:0000654,benign connective and soft tissue neoplasm,"['benign connective and soft tissue tumor', 'connective and soft tissue neoplasm, benign', 'benign tumor of the soft tissue and bone', 'connective tissue benign neoplasm', 'soft tissue benign neoplasm', 'benign mesenchymal cell neoplasm', 'benign connective and soft tissue tumour', 'tumour of the soft tissue', 'neoplasm of soft tissue', 'neoplasm of soft tissues', 'tumor of the soft tissue', 'benign tumour of the soft tissue and bone', 'benign neoplasm of the soft tissue and bone', 'benign connective and soft tissue neoplasm']",0060123,,,,,C53684,,,,,,
mondo:0000659,delta-heavy chain disease,['delta heavy chain disease'],0060129,,,C0272253,,,,,203.80,,,
mondo:0000660,akinetopsia,,0060130,,,,,,,,,,,
mondo:0000661,alexithymia,,0060131,,,,,,,,,,,
mondo:0000662,amusia,['receptive amusia'],0060132,,,C0234497,,,,,,,,
mondo:0000663,anosognosia,,0060133,,,,,,,,,,,
mondo:0000664,apperceptive agnosia,,0060134,,,,,,,,,,,
mondo:0000665,apraxia,"['dyspraxia', 'Apraxias']",0060135,,,,,C180557,,D001072,,R48.2,,
mondo:0000666,associative visual agnosia,['associative agnosia'],0060136,,,,,,,,,,,
mondo:0000667,auditory agnosia,,0060137,,,,,,,,,,,
mondo:0000668,autotopagnosia,,0060138,,,,,,,,,,,
mondo:0000669,color agnosia,,0060139,,,,,,,,,,,
mondo:0000670,cortical deafness,,0060140,,,C0392704,,,,,,,,
mondo:0000671,finger agnosia,"['finger agnosia (disease)', 'finger agnosia', 'manual digit agnosia']",0060141,,,,,,,,,,,0010525
mondo:0000672,form agnosia,,0060142,,,,,,,,,,,
mondo:0000673,integrative agnosia,,0060143,,,,,,,,,,,
mondo:0000674,mirror agnosia,,0060144,,,,,,,,,,,
mondo:0000675,pain agnosia,['analgesia'],0060145,,,,,C125664,1001484,,,,,
mondo:0000676,phonagnosia,,0060146,,,,,,,,,,,
mondo:0000677,semantic agnosia,,0060147,,,,,,,,,,,
mondo:0000678,simultanagnosia,,0060148,,,,,,,,,,,
mondo:0000679,social emotional agnosia,['expressive agnosia'],0060149,,,,,,,,,,,
mondo:0000680,astereognosia,"['somatosensory agnosia', 'astereognosia (disease)', 'astereognosia']",0060150,,,,,,,,,,,0010527
mondo:0000681,tactile agnosia,,0060151,,,,,,,,,,,
mondo:0000682,time agnosia,,0060152,,,,,,,,,,,
mondo:0000683,topographical agnosia,,0060153,,,,,,,,,,,
mondo:0000684,verbal auditory agnosia,,0060154,,,,,,,,,,,
mondo:0000685,visual agnosia,"['visuoperceptual agnosia', 'visual agnosia', 'visual agnosia (disease)']",0060155,,,,,C35276,,,,,,0030222
mondo:0000686,alexia without agraphia,"['visual verbal Agnosias', 'alexias, Pure', 'Pure alexia', 'Agnosias, visual verbal', 'Pure alexia without agraphia', 'agraphia, alexia without', 'verbal Agnosias, visual', 'alexia without Agraphias', 'without agraphia, alexia', 'without Agraphias, alexia', 'Pure Word blindness', 'agnosia, visual verbal', 'Word blindness, Pure', 'Agraphias, alexia without', 'alexia without agraphia', 'visual verbal agnosia', 'Blindnesses, Pure Word', 'Pure alexias', 'verbal agnosia, visual', 'Word Blindnesses, Pure', 'blindness, Pure Word', 'alexia syndrome without agraphia', 'Pure Word Blindnesses']",0060156,,,,,,,D020237,,,,
mondo:0000687,diffuse alopecia areata,"['marginal alopecia', 'Jonston^s alopecia', 'Cazenave^s vitiligo', 'Celsus^ vitiligo', 'patchy alopecia', 'alopecia celsi']",0060157,,,,,,,C531609,,,,
mondo:0000688,inborn organic aciduria,"['inherited organic acidemia', 'organic acidemia', 'disorder of organic acid metabolism', 'rare inborn error of organic acid metabolic process', 'inborn error of organic acid metabolic process', 'inborn organic acid metabolic process disorder', 'organic acid metabolism disorder', 'organic aciduria']",0060159,,289899,C1263739,,C101334,,,277.89,,,
mondo:0000690,body dysmorphic disorder,"['dysmorphophobia', 'dysmorphic syndrome', 'body dysmorphia']",0060163,,,,,,,D057215,,F45.22,,
mondo:0000693,bipolar II disorder,['bipolar ll disorder'],0060166,,,,,,,,296.89,,,
mondo:0000694,seasonal affective disorder,"['sad', 'winter depression', 'SADS']",0060167,,,,,,,D016574,296.99,,,
mondo:0000698,gamma-amino butyric acid metabolism disorder,,0060176,,,,,,,,,,,
mondo:0000700,familial hemiplegic migraine,"['FHM', 'hemiplegic-ophthalmoplegic migraine', 'hemiplegic migraine, familial', 'hereditary hemiplegic migraine']",0060178,,569,,"['0.2002', '-0.442', '0.010345', '0.3013', '-0.0696', '0.073', '-0.0717', '0.01794', '-0.5767', '-0.1167', '0.0931', '0.157', '0.10016', '0.2744', '-0.651', '-0.2205', '-0.309', '-0.2944', '-0.784', '-0.1245', '-0.2145', '-0.1719', '-0.001873', '-0.3235', '-0.2666', '-0.542', '0.2683', '-0.492', '-0.2998', '-0.616', '0.922', '-0.2319', '0.309', '-0.016', '-0.2299', '0.557', '-0.8853', '-0.5806', '-0.1929', '-0.4363', '1.214', '-0.3967', '0.2158', '-0.434', '0.6074', '-0.6133', '-0.5244', '0.1957', '-0.624', '0.818', '-0.5635', '0.0976', '0.0695', '0.1252', '1.13', '0.2499', '0.405', '-0.298', '-0.4712', '-0.1053', '-0.2961', '0.1059', '0.2888', '0.08765', '-0.637', '0.3425', '0.4578', '1.05', '0.3936', '0.1885', '0.1302', '0.302', '0.5483', '-1.153', '0.4253', '0.7905', '-0.2196', '1.012', '0.2003', '0.03934', '0.139', '0.2625', '-0.1144', '-0.2249', '0.3445', '-0.1853', '0.4468', '0.4875', '0.591', '0.1826', '-0.259', '-0.1191', '-0.02884', '-0.1359', '-0.0007553', '0.1274', '-0.267', '-0.6304', '0.1556', '0.02078']",C117009,,,346.8,,,
mondo:0000701,ischemic colitis,['colonic ischemia'],0060181,,,C0162529,,,,D017091,,,,
mondo:0000702,microscopic colitis,,0060182,,58220,C0400821,,C38504,1001295,D046728,558.9,,,
mondo:0000703,collagenous colitis,,0060183,,36205,C0238067,,C27021,1001293,D046729,558.9,K52.831,10048928,
mondo:0000704,lymphocytic colitis,,0060184,,65279,C0400822,,C27147,1001294,D046730,558.9,K52.832,10025268,
mondo:0000705,Clostridium difficile colitis,"['Clostridium difficile infection', 'C. diff infection', 'Clostridioides difficile caused colitis (disease)', 'C. diff colitis', 'pseudomembranous colitis']",0060185,,,,,C35286,0009130,D004761,,,10009657,
mondo:0000706,chemical colitis,,0060186,,,,,,,,558.9,,,
mondo:0000707,diversion colitis,,0060187,,,C0267532,,,,,558.9,,,
mondo:0000708,Crohn jejunoileitis,['jejunoileitis'],0060188,,,,,,,,,,,
mondo:0000709,Crohn ileitis,"['Crohn^s ileitis', 'ileitis']",0060189,,,C0020877,,C35329,,D007079,558.9,,10021312,
mondo:0000710,gastroduodenal Crohn disease,"['gastroduodenal Crohn^s disease', 'upper GI Crohn^s disease']",0060191,,,,,,,,,,,
mondo:0000715,lymph node adenoid cystic carcinoma,"['lymph node adenoid cystic carcinoma', 'lymph node adenoid cystic cancer']",0060219,,,,,,,,,,,
mondo:0000716,agraphia,,0060223,,,,,,,D000381,,,,
mondo:0000721,xanthinuria,,,,,,,,,,277.2,,,
mondo:0000722,non-syndromic synpolydactyly,"['nonsyndromic synpolydactyly', 'synpolydactyly']",0060242,,,,,C75003,,C538153,,,,
mondo:0000723,stutter disorder,"['stutter', 'stammering', 'stuttering', 'stuttering, familial persistent', 'familial persistent stuttering']",0060243,,,,,C35043,,,,,,
mondo:0000724,specific language impairment,,0060244,,458713,C0454651,,,,,,,,
mondo:0000726,idiopathic scoliosis,,0060250,,,CN241052,,,,,,,,
mondo:0000727,scapuloperoneal myopathy,"['scapuloperoneal syndrome, myopathic type', 'myopathy, scapuloperoneal']",0060253,,,C2931268,,,,C536624,,,,
mondo:0000728,ptosis,"['ptosis', 'ptosis (disease)', 'eyelid ptosis', 'drooping eyelid', 'blepharoptosis']",0060260,,,C0033377,,C27298,,D001763,374.30,,,0000508
mondo:0000732,combined oxidative phosphorylation deficiency,,0060286,,,,"['-0.05334', '0.03772', '0.00794', '-0.001386', '0.00883', '-0.05643', '0.02461', '0.0421', '-0.03235', '-0.006874', '-0.00555', '-0.005177', '-2.295e-05', '0.003069', '0.01075', '-0.0335', '-0.00882', '-0.01837', '-0.03134', '-0.0815', '-0.00919', '-0.0359', '0.04056', '0.001758', '0.007168', '-0.00921', '0.0156', '-0.003832', '0.000851', '-0.04388', '0.03687', '0.01557', '0.0695', '0.01521', '0.01038', '-0.04065', '-0.007217', '-0.02406', '-0.003487', '-0.04004', '0.0192', '-0.04843', '0.01889', '0.013', '-0.03017', '-0.05157', '0.0003376', '0.02089', '0.002777', '0.02213', '-0.02075', '-0.0262', '0.01069', '0.005795', '-0.03815', '-0.01512', '0.03897', '-0.01616', '-0.04312', '0.01479', '0.03528', '0.03058', '0.04498', '-0.012146', '0.00489', '0.01584', '0.05154', '0.02989', '-0.05356', '0.056', '-0.02951', '0.002085', '0.003124', '-0.03644', '0.03687', '0.02296', '0.01317', '-0.01052', '-0.01817', '0.01149', '-0.0088', '0.014336', '-0.01958', '0.03035', '0.01355', '-0.013306', '0.01926', '0.04227', '0.0554', '0.02179', '0.0317', '0.0325', '-0.0047', '0.00231', '0.0972', '0.04675', '0.0253', '-0.07166', '-0.006603', '0.01947']",,,,,,,
mondo:0000733,cornea plana,['flat cornea'],0060287,,,,,,,,,,,0007720
mondo:0000734,Ohdo syndrome and variants,"['Ohdo blepharophimosis syndrome', 'Ohdo syndrome']",0060289,,,,,,,,,,,
mondo:0000736,dyschromatosis universalis hereditaria,"['DUH', 'dyschromatosis universalis']",0060304,,241,C2930995,"['-0.1628', '0.4873', '-0.263', '-0.213', '0.281', '-0.1593', '-0.3044', '-0.1705', '-0.2395', '-0.0569', '-0.1121', '0.138', '-0.1848', '-0.10333', '-0.141', '0.4016', '0.4614', '-0.2815', '-0.09467', '-0.6313', '-0.327', '0.058', '0.5254', '-0.11694', '-0.1648', '0.275', '-0.1677', '-0.11053', '-0.0229', '0.1205', '0.5005', '-0.4329', '0.0294', '-0.012146', '0.305', '0.1235', '-0.08856', '-0.1368', '-0.000662', '-0.344', '-0.03992', '-0.3428', '0.1744', '0.03406', '0.09827', '-0.2078', '-0.251', '0.2568', '0.2773', '0.09015', '0.1378', '-0.003765', '0.2439', '0.02469', '-0.3796', '-0.3635', '0.2693', '0.2043', '-0.5884', '-0.3286', '0.1366', '-0.2035', '0.05396', '0.03543', '-0.1089', '0.06384', '0.543', '0.4722', '0.004726', '0.613', '-0.304', '-0.437', '0.1532', '0.4214', '0.0788', '0.1216', '-0.2395', '0.1266', '-0.07904', '-0.6025', '0.096', '-0.16', '0.538', '0.12225', '-0.01636', '-0.2317', '-0.2002', '0.3286', '0.1029', '0.2181', '0.417', '0.396', '0.153', '0.2135', '0.4224', '0.01814', '0.5713', '-0.4387', '0.10925', '0.4124']",C173131,,C535730,,,,
mondo:0000739,uvulitis,"['acute uvulitis', 'palatine uvula inflammation']",0060310,,,C0042174,,C128385,,,528.3,,10051962,
mondo:0000740,adenoid hypertrophy,"['enlarged adenoids', 'adenoidal hypertrophy']",0060311,,,C0149825,,,,,474.12,,10001229,
mondo:0000741,angular cheilitis,"['angular cheilitis', 'angular stomatitis', 'perleche', 'cheilitis of angle of oral opening', 'cheilosis', 'angle of oral opening cheilitis', 'perlèche', 'angular cheilosis', 'commissural cheilitis']",0060312,,,C0221264,,C112198,,,,,,
mondo:0000743,oral hairy leukoplakia,"['hairy leukoplakia of the mouth', 'hairy leukoplakia of oral mucosa', 'oral cavity hairy leukoplakia', 'hairy leukoplakia', 'hairy leukoplakia of mouth', 'hairy leukoplakia of the oral mucosa', 'oral hairy keratosis', 'mouth hairy leukoplakia']",0060315,,,C0206186,,C3722,,D017733,528.6,K13.3,,
mondo:0000744,lung abscess,"['lung abscess (disease)', 'lung abscess']",0060317,,,C0024110,,C99090,1001362,D008169,513.0,,,0025044
mondo:0000745,cardiac arrest,"['circulatory arrest', 'cardiopulmonary arrest']",0060319,,,C0444720,,,,D006323,427.5,I46,,
mondo:0000748,mastoiditis,"['mastoid process of temporal bone inflammation', 'mastoiditis', 'mastoid process of temporal boneitis', 'mastoiditis (disease)']",0060322,,,C0024904,,C128368,,D008417,383.9,,,0000265
mondo:0000749,breast abscess,,0060323,,,C0151463,,,,,,,,
mondo:0000750,dental abscess,,0060324,,,C0518988,,,,,,,,
mondo:0000751,cervical polyp,"['polyp of cervix', 'cervix adenomatous polyp', 'adenomatous polyp of the cervix', 'uterine cervix polyp', 'adenomatous polyp of the uterine cervix', 'cervix uteri adenomatous polyp', 'polyp of uterine cervix', 'cervical polyp', 'cervix polyp', 'polyp of cervix uteri', 'cervical polyp (disease)', 'uterine cervix adenomatous polyp', 'polyp of the uterine cervix', 'adenomatous polyp of cervix', 'polyp of the cervix uteri', 'polyp of the cervix', 'cervix uteri polyp', 'adenomatous polyp of uterine cervix']",0060325,,,C0347493,,C2939,,,219,,,0030159
mondo:0000754,anal fistula,"['anal fistula (disease)', 'anal fistula', 'anorectal fistula']",0060328,,228113,,,C60785,,D012003,,K60.3,,0010447
mondo:0000755,ectopic pregnancy,"['eccyesis', 'pregnancy, ectopic', 'extrauterine pregnancy']",0060329,,,,,C34945,,D011271,633.90,,,
mondo:0000756,parameningeal embryonal rhabdomyosarcoma,,0060338,,,,,,,,,,,
mondo:0000757,glucocorticoid-induced osteoporosis,['steroid-induced osteoporosis'],0060343,,,,,,,,,,,
mondo:0000758,bacillary angiomatosis,"['bacillary Angiomatoses', 'epithelioid Angiomatoses, bacillary', 'bacillary angiomatosis', 'angiomatosis, bacillary epithelioid', 'angiomatosis, epithelioid', 'angiomatoses, bacillary epithelioid', 'bacillary epithelioid angiomatosis', 'angiomatoses, epithelioid', 'epithelioid angiomatosis, bacillary', 'epithelioid angiomatosis', 'bacillary epithelioid Angiomatoses', 'angiomatoses, bacillary', 'Bartonella caused angiomatosis', 'epithelioid Angiomatoses']",0060345,,,C0085434,,C3477,,D016917,083.8,,,
mondo:0000761,syndrome caused by partial chromosomal deletion,"['chromosomal deletion syndrome', 'microdeletion syndrome']",0060388,,,,,,,,,,,
mondo:0000762,syndrome caused by partial chromosomal duplication,"['microduplication sydrome', 'chromosomal duplication syndrome']",0060429,,,,,,,,,,,
mondo:0000763,epithelial and subepithelial corneal dystrophy,['epithelial and subepithelial dystrophy'],0060440,,,,,,,,,,,
mondo:0000764,epithelial-stromal TGFBI dystrophy,['TGFBI corneal dystrophy (disease)'],0060441,,,,,,,,,,,
mondo:0000766,corneal endothelial dystrophy,['endothelial dystrophy'],0060443,,,,,,,,371.57,,,
mondo:0000771,allergic respiratory disease,"['allergic form of respiratory system disease', 'airway allergy']",0060496,,,,,,,,,,,
mondo:0000774,autoimmune neuropathy,['autoimmune peripheral neuropathy'],0060499,,,,,,,,,,,
mondo:0000775,drug allergy,['allergy of exposure to drug'],0060500,,,,,,,D004342,,,,
mondo:0000777,gastrointestinal allergy,"['digestive tract allergic disease', 'allergic disease of digestive tract']",0060502,,,,,,,,,,,
mondo:0000807,latex allergy,,0060532,,,,,,,D020315,V15.07,,,
mondo:0000809,purpura fulminans,"['fibrinolytic purpura', 'purpura gangrenosa']",0060538,,,,,,1001913,D055665,,,,
mondo:0000811,anomalous left coronary artery from the pulmonary artery,"['ALCAPA disorder', 'White-Garland syndrome', 'Bland-White-Garland syndrome', 'ALCAPA', 'BWGS']",0060562,,,C1735886,,,,D063748,,,,
mondo:0000812,vertebral column disorder,"['disease of vertebral column', 'vertebral column disease or disorder', 'disorder of vertebral column', 'vertebral column disease', 'spinal disease']",0060564,,,C0037933,,,,D013122,724.9,,,
mondo:0000813,cardiac tuberculosis,['cardiovascular tuberculosis'],0060570,,,C0041308,,,1001442,D014381,,,,
mondo:0000814,B-cell adult acute lymphocytic leukemia,"['adult B cell acute lymphocytic leukaemia', 'B cell adult acute lymphocytic leukemia', 'B-cell adult acute lymphoblastic leukaemia', 'adult B-cell acute lymphoblastic leukaemia', 'adult B cell acute lymphoblastic leukaemia', 'B cell adult acute lymphocytic leukaemia', 'adult B-cell childhood acute lymphoblastic leukaemia', 'adult B-lymphoblastic leukaemia', 'adult B-cell ALL', 'B-cell adult acute lymphoblastic leukemia', 'adult B-cell lymphocytic leukemia', 'B cell adult acute lymphoblastic leukemia', 'B cell adult acute lymphoblastic leukaemia', 'adult B-cell acute lymphoblastic leukemia', 'adult B acute lymphoblastic leukemia', 'B-cell childhood acute lymphoblastic leukaemia of adults', 'adult B-cell acute lymphocytic leukemia', 'adult B cell acute lymphoblastic leukemia', 'adult B cell acute lymphocytic leukemia', 'adult B cell ALL', 'B acute lymphoblastic leukaemia', 'adult precursor B-lymphoblastic leukemia', 'adult B-cell acute lymphocytic leukaemia', 'adult B acute lymphoblastic leukaemia', 'adult B-lymphoblastic leukemia', 'B acute lymphoblastic leukemia', 'B cell adult ALL', 'B-cell childhood acute lymphoblastic leukemia of adults', 'adult precursor B-lymphoblastic leukaemia', 'adult B-cell lymphocytic leukaemia', 'adult B-cell childhood acute lymphoblastic leukemia', 'B-cell adult ALL']",0060592,,,C0279593,,C9143,1001935,,,,,
mondo:0000815,fetal nicotine spectrum disorder,,0060606,,,,,,,,,,,
mondo:0000816,abdominal obesity-metabolic syndrome,"['metabolic syndrome X', 'metabolic syndrome']",0060611,,411969,C2930930,"['-0.04333', '0.02884', '0.01259', '-0.02628', '0.01322', '-0.04956', '-0.014595', '0.0845', '-0.05103', '-0.02136', '-0.00172', '-0.00885', '0.002052', '0.0379', '-0.04688', '-0.02502', '0.006023', '-0.004036', '-0.03053', '-0.0888', '0.00618', '-0.02156', '0.03632', '-0.02815', '0.02927', '-0.0356', '0.01953', '0.02792', '0.02843', '-0.03345', '0.0525', '-0.0324', '0.0625', '0.02826', '0.009056', '-0.007523', '-0.03065', '-0.000353', '-0.01407', '-0.03503', '0.002897', '-0.04596', '0.02733', '-0.03946', '0.02399', '-0.03967', '-0.02728', '0.0402', '0.00784', '0.01153', '-0.03775', '0.0001605', '0.01614', '0.01447', '-0.02483', '-0.007385', '0.0352', '-0.01767', '-0.04837', '0.000977', '0.06415', '0.01688', '-0.01582', '0.001333', '-0.005238', '-0.007565', '0.0737', '0.05966', '-0.03146', '0.0847', '-0.0565', '0.01591', '0.01369', '-0.04846', '0.03244', '0.0385', '0.02728', '0.01167', '-0.03278', '-0.03787', '-0.00784', '-0.009575', '-0.02397', '0.00813', '-0.02391', '-4.16e-05', '0.0359', '0.0484', '0.05878', '-0.0268', '0.0001715', '0.02975', '0.02132', '0.02917', '0.1411', '0.0181', '0.02766', '-0.09235', '0.003265', '0.01256']",C84442,0000195,C535554,277.7,E88.81,,
mondo:0000819,anencephaly,['anencephalus'],0060668,,,,,C84560,,D000757,,,,
mondo:0000820,cerebral cavernous malformation,"['CCM', 'cavernous angiomatous malformations', 'familial cavernous angioma', 'brain cavernous hemangioma', 'cerebral capillary malformations']",0060669,,164,,,C84626,,,,,,
mondo:0000824,congenital diarrhea,"['diarrhea, congenital']",0060774,,,CN232319,,,,,,,,
mondo:0000827,salmonellosis,"['infections, Salmonella', 'Salmonella infection', 'rare form of salmonellosis']",0060859,,795,CN205993,,C157974,1001418,D012480,003.9,,10039447,
mondo:0000828,juvenile-onset Parkinson disease,['juvenile-onset Parkinson^s disease'],0060893,,,,,,,,,,,
mondo:0000831,thrombotic disease,"['clot, blood', 'Thromboses', 'blood Clots', 'thrombosis', 'thrombotic disorder', 'Clots, blood', 'thrombus', 'blood clot']",0060903,,,,,C26891,,D013927,453.9,,,
mondo:0000833,bone remodeling disease,,0080005,,,,,,,,,,,
mondo:0000836,disease of bone structure,['bone structure disease'],0080010,,,,,,,,,,,
mondo:0000837,bone resorption disease,,0080011,,,,,,,D001862,,,,
mondo:0000840,dysbaric osteonecrosis,"['caisson disease of bone', 'DON']",0080018,,,,,,,,,,,
mondo:0000845,fibrous dysplasia,['fibrous dysplasia of bone'],0080031,,249,,"['0.01695', '-0.4966', '0.3098', '-0.5396', '0.655', '-0.01971', '0.1934', '1.295', '-0.9785', '-0.3257', '-0.2233', '0.3794', '-0.01828', '0.521', '-0.3936', '-0.01201', '0.102', '-0.0971', '-0.655', '-0.4937', '0.2522', '-0.326', '0.7085', '-0.434', '0.05704', '0.4565', '-0.07336', '-0.611', '0.1809', '0.4326', '0.442', '-0.3071', '-0.0636', '-0.3179', '0.08246', '-0.1755', '0.04266', '-0.607', '-0.2734', '0.0636', '0.5366', '0.02226', '0.4304', '-0.0946', '0.3594', '0.1477', '-0.907', '-0.4216', '0.4985', '0.02472', '0.2861', '-0.1733', '0.5024', '0.0181', '-0.3772', '-0.4062', '0.2012', '-0.3054', '0.0659', '-0.3032', '0.6436', '-0.652', '-0.316', '-0.04807', '-0.2854', '0.6', '0.2703', '0.955', '0.1742', '0.448', '0.4795', '0.313', '0.1074', '-0.12445', '0.6567', '0.01199', '0.0855', '0.298', '0.12067', '-0.589', '-0.299', '-0.2903', '0.894', '-0.0004385', '-0.3901', '-0.55', '0.429', '-0.06033', '-0.08826', '0.37', '0.1271', '-0.03827', '-0.5107', '-0.448', '0.9663', '0.007782', '0.0656', '0.1584', '0.4783', '0.1023']",C34609,,D005357,733.29,,10016664,
mondo:0000849,fibrogenesis imperfecta ossium,['baker^s disease'],0080040,,,,,,,,,,,
mondo:0000858,neuronal intestinal dysplasia,,0080072,,,C0345244,,,,,751.5,,,
mondo:0000859,spina bifida occulta,"['spina bifida occulta', 'spina bifida occulta (disease)', 'closed spinal dysraphism']",0080073,,,,,C101044,,D016136,756.17,,,0003298
mondo:0000863,"myopathy, lactic acidosis, and sideroblastic anemia","['mitochondrial myopathy and sideroblastic anemia', 'MLASA', 'sideroblastic anemia and mitochondrial myopathy', 'sideroblastic anaemia and mitochondrial myopathy', 'myopathy, lactic acidosis, and siderblastic anemia', 'myopathy, lactic acidosis and sideroblastic anemia', 'myopathy with lactic acidosis and sideroblastic anemia', 'myopathy, lactic acidosis and sideroblastic anaemia', 'myopathy with lactic acidosis and sideroblastic anaemia', 'mitochondrial myopathy and sideroblastic anaemia', 'MSA', 'myopathy, lactic acidosis, and siderblastic anaemia']",0080099,,2598,CN220387,"['-0.717', '0.4224', '-0.12354', '0.465', '0.8223', '-0.04587', '-0.2532', '0.4658', '-0.1837', '-0.4365', '0.6504', '-0.266', '0.2825', '0.2377', '-1.054', '0.03836', '-0.4517', '0.2463', '-0.5957', '-0.2205', '-0.0645', '-0.5083', '-0.04324', '0.00418', '0.3691', '-0.4414', '-0.1243', '-0.1401', '0.3613', '0.2241', '0.252', '0.3662', '0.526', '0.571', '0.3374', '-0.2338', '-0.7617', '-0.5605', '0.5425', '0.0783', '-0.786', '-0.06064', '0.001733', '-0.1527', '-0.788', '-0.7983', '0.1604', '0.10925', '0.2477', '-0.4165', '0.3333', '0.4238', '0.8267', '-0.3057', '0.6665', '-0.985', '0.3186', '0.2915', '-0.9326', '0.04904', '0.0905', '0.3967', '0.0765', '-0.543', '-0.397', '0.3862', '0.2585', '0.9736', '-0.5737', '0.8184', '0.671', '-0.296', '-0.521', '-0.446', '0.3684', '1.134', '0.0636', '0.06003', '0.1338', '0.759', '0.0754', '0.1978', '0.02756', '0.01233', '0.662', '-0.1459', '-0.1492', '0.2795', '0.7935', '-0.2313', '0.648', '0.1337', '-0.0966', '-0.06555', '0.8257', '0.8115', '0.4067', '0.1517', '0.09467', '-0.597']",,,C536101,,,,
mondo:0000866,hereditary myoglobinuria,['myoglobinurias'],0080108,,,,,C114705,,D009212,,R82.1,,0002913
mondo:0000870,childhood acute lymphoblastic leukemia,"['childhood acute lymphogenous leukaemia', 'pediatric acute lymphocytic leukemia', 'pediatric ALL', 'pediatric acute lymphoid leukemia', 'acute lymphoblastic leukemia (ALL)', 'acute lymphoblastic leukaemia (ALL)', 'childhood acute lymphoblastic leukemia', 'childhood acute lymphogenous leukemia', 'childhood acute lymphocytic leukemia', 'childhood ALL', 'paediatric acute lymphocytic leukaemia', 'paediatric acute lymphogenous leukaemia', 'childhood precursor lymphoblastic leukemia', 'pediatric acute lymphocytic leukemia (ALL)', 'childhood acute lymphoid leukemia', 'paediatric ALL', 'childhood acute lymphocytic leukaemia', 'paediatric acute lymphoblastic leukaemia', 'childhood acute lymphoid leukaemia', 'childhood precursor lymphoblastic leukaemia', 'paediatric acute lymphoid leukaemia', 'pediatric acute lymphogenous leukemia', 'paediatric acute lymphocytic leukaemia (ALL)', 'pediatric acute lymphoblastic leukemia']",0080144,,,,,C3168,,,,,,
mondo:0000871,T-cell childhood acute lymphocytic leukemia,"['T-cell paediatric acute lymphocytic leukaemia', 'T-cell paediatric ALL', 'childhood T-cell acute lymphoblastic leukemia', 'T-cell childhood ALL', 'T-cell pediatric acute lymphocytic leukemia', 'childhood T-cell acute lymphoblastic leukaemia', 'T-cell childhood acute lymphocytic leukemia', 'childhood T acute lymphoblastic leukemia', 'T-cell childhood acute lymphoblastic leukemia', 'T-cell childhood acute lymphoblastic leukaemia', 'childhood T acute lymphoblastic leukaemia', 'childhood precursor T-lymphoblastic leukaemia', 'T-cell pediatric ALL', 'T acute lymphoblastic leukaemia', 'T-cell paediatric acute lymphoblastic leukaemia', 'childhood precursor T-lymphoblastic leukemia', 'childhood T-ALL', 'T-cell pediatric acute lymphoblastic leukemia', 'T acute lymphoblastic leukemia']",0080145,,,C0279583,,C7953,1001947,,,,,
mondo:0000872,B-cell childhood acute lymphoblastic leukemia,"['B-cell pediatric acute lymphocytic leukemia', 'B-cell paediatric acute lymphocytic leukaemia', 'B-cell paediatric acute lymphoblastic leukaemia', 'childhood precursor B-lymphoblastic leukaemia', 'B-cell childhood acute lymphogenous leukaemia', 'B cell paediatric ALL', 'B-cell childhood acute lymphocytic leukaemia', 'B cell childhood acute lymphocytic leukemia', 'childhood precursor B-lymphoblastic leukemia', 'B cell pediatric ALL', 'B cell childhood acute lymphoblastic leukemia', 'B-cell childhood acute lymphocytic leukemia', 'B-cell paediatric ALL', 'B-cell pediatric acute lymphoblastic leukemia', 'B-cell childhood acute lymphoid leukaemia', 'B-cell pediatric acute lymphogenous leukemia', 'childhood B acute lymphoblastic leukaemia', 'childhood B-ALL', 'B-cell childhood ALL', 'B cell pediatric acute lymphoblastic leukemia', 'B-cell pediatric acute lymphoid leukemia', 'B cell childhood acute lymphocytic leukaemia', 'B acute lymphoblastic leukaemia', 'B cell pediatric acute lymphocytic leukemia', 'B cell paediatric acute lymphocytic leukaemia', 'B-cell childhood acute lymphoid leukemia', 'B-cell paediatric acute lymphogenous leukaemia', 'B-cell pediatric ALL', 'B cell childhood ALL', 'B cell paediatric acute lymphoblastic leukaemia', 'B acute lymphoblastic leukemia', 'childhood B acute lymphoblastic leukemia', 'B-cell paediatric acute lymphoid leukaemia', 'B cell childhood acute lymphoblastic leukaemia', 'B-cell childhood acute lymphogenous leukemia']",0080146,,,C0279584,,C9140,1001946,,,,,
mondo:0000873,lymphoblastic lymphoma,"['precursor lymphoblastic lymphoma', 'lymphoblastic lymphoma', 'lymphoma, lymphoblastic, malignant', 'precursor cell lymphoblastic lymphoma', 'lymphoma, lymphoblastic']",0080147,,,C0079748,,C9360,,,202.80,,,
mondo:0000874,T-cell childhood lymphoblastic lymphoma,"['childhood T lymphoblastic lymphoma', 'T lymphoblastic lymphoma', 'childhood precursor T-lymphoblastic lymphoma']",0080148,,,C1332998,,C7210,1001948,,,,,
mondo:0000875,adult acute monocytic leukemia,"['acute monocytic leukemia of adults', 'M5b adult acute leukemia', 'adult acute differentiated monocytic leukaemia (M5b)', 'acute monocytic leukaemia of adults', 'M5b adult acute differentiated monocytic leukemia', 'adult acute monocytic leukemia', 'M5b adult acute leukaemia', 'adult acute differentiated monocytic leukemia (M5b)', 'acute monocytic leukemia', 'acute monocytic leukaemia', 'M5b adult acute differentiated monocytic leukaemia']",0080149,,,C0280634,,C8263,,,,,,
mondo:0000878,cytomegalovirus retinitis,"['CMV retinitis', 'Retinitis, Cytomegaloviral', 'Cytomegaloviral Retinitis', 'Cytomegalovirus caused retinitis']",0080160,,,C0206178,,C50521,1001302,D017726,,,,
mondo:0000879,cutaneous candidiasis,['zone of skin candidiasis'],0080161,,,C0006846,,,,D002179,,,,
mondo:0000884,myeloid and lymphoid neoplasms associated with FGFR1 abnormalities,,0080167,,,,,C84277,,,,,,
mondo:0000888,gastrointestinal mucositis,"['gastrointestinal system mucosa inflammation', 'mucositis', 'gastrointestinal system mucosaitis']",0080178,,,C0521585,,C3853,,,558.9,,,
mondo:0000889,haemophilus meningitis,"['Haemophilus influenzae caused bacterial meningitis', 'Haemophilus influenzae bacterial meningitis']",0080179,,,,,,1000955,D008583,320.0,,10018953,
mondo:0000890,Zika virus congenital syndrome,"['congenital Zika syndrome', 'congenital Zika virus infection', 'ZIKV congenital infection']",0080180,,,,,,,D000071243,,,,
mondo:0000891,mixed fibrolamellar hepatocellular carcinoma,,0080182,,,,,,,,,,,
mondo:0000892,colon medullary carcinoma,"['colon medullary carcinoma', 'medullary colon carcinoma', 'medullary carcinoma of the colon']",0080183,,,C1880119,,C60641,,,,,,
mondo:0000893,mixed mucinous and nonmucinous bronchioloalveolar adenocarcinoma,"['mixed mucinous and non-mucinous bronchioloalveolar adenocarcinoma', 'indeterminate bronchioloalveolar carcinoma', 'mixed mucinous and non-mucinous bronchioloalveolar carcinoma', 'mixed mucinous and non-mucinous bronchoalveolar lung carcinoma', 'mixed mucinous and non-mucinous bronchioloalveolar lung carcinoma']",0080184,,,C1266036,,C7270,,,,,,
mondo:0000894,mucinous bronchioloalveolar adenocarcinoma,,0080185,,,,,,,,,,,
mondo:0000895,nonmucinous bronchioloalveolar adenocarcinoma,,0080186,,,,,,,,,,,
mondo:0000898,malignant hemangioma,"['hemangioma, malignant']",0080189,,,C0474836,,,,,,,,
mondo:0000901,relapsed/refractory diffuse large B-cell lymphoma,,0080192,,,,,,,,,,,
mondo:0000902,agenesis of the corpus callosum with peripheral neuropathy,"['ACCPN', 'Charlevoix disease', 'corpus callosum agenesis-neuronopathy syndrome', 'HMSN/ACC', 'agenesis of corpus callosum with neuronopathy', 'polyneuropathy, sensorimotor, with or without agenesis of the corpus callosum', 'peripheral neuropathy associated with agenesis of the corpus callosum', 'agenesis of the corpus callosum with peripheral neuropathy', 'hereditary motor and sensory neuropathy with agenesis of the corpus callosum', 'agenesis of corpus callosum with polyneuropathy', 'corpus callosum agenesis neuronopathy', 'Andermann syndrome', 'agenesis of corpus callosum with peripheral neuropathy', 'corpus callosum, agenesis of, with neuronopathy']",0090003,218000,1496,C0795950,"['0.4958', '0.726', '-0.4666', '0.596', '-0.1832', '-0.04895', '-0.222', '0.1804', '-0.04147', '-0.2277', '0.2427', '-0.2544', '0.3752', '0.3372', '-0.4983', '0.191', '-0.3743', '0.2434', '-0.792', '-0.297', '0.433', '-0.402', '-0.1626', '0.2426', '0.188', '0.0573', '-0.1956', '-0.1719', '-0.09235', '-1.231', '0.2556', '-0.01216', '0.434', '-0.4453', '0.1509', '-0.2339', '-0.522', '-0.603', '-0.002602', '-0.314', '-0.4363', '-0.3972', '-0.4036', '0.4075', '-0.1539', '-0.574', '0.5645', '-0.01434', '0.423', '0.0678', '-0.57', '0.4116', '0.0601', '-0.09515', '-0.01354', '-0.263', '0.01514', '-0.4744', '-0.815', '-0.484', '-0.596', '0.09106', '-0.1498', '0.5454', '-0.0563', '0.4211', '0.2056', '0.9795', '-0.2003', '0.21', '-0.2042', '0.2786', '-0.3289', '-0.6016', '0.484', '0.435', '0.1231', '0.3923', '-0.05093', '-0.0415', '-0.4102', '-0.4792', '-0.2703', '0.199', '-0.007725', '0.167', '0.04166', '0.2488', '0.3794', '0.05893', '0.1157', '0.3005', '-0.3145', '-0.01316', '-0.1295', '-0.198', '-0.454', '0.1818', '0.3943', '-0.0745']",,,C536446,,,,
mondo:0000903,myoclonus-dystonia syndrome,"['myoclonus-dystonia', 'dystonia, alcohol responsive', 'hereditary essential myoclonus', 'dystonia-11, myoclonic', 'DYT11', 'myoclonus-Dystonia', 'myoclonic dystonia', 'Hereditary essential myoclonus', 'alcohol-responsive dystonia', 'DYT-SGCE', 'myoclonus, hereditary essential', 'dystonia, alcohol-responsive', 'dystonia with myoclonus', 'dystonia 11, myoclonic', 'dystonia 11', 'myoclonus-dystonia syndrome']",0090033,,36899,C1834570,"['0.3875', '0.329', '-0.2979', '-0.5986', '-0.641', '-0.7183', '0.605', '0.1722', '-0.225', '-0.4072', '0.2954', '0.476', '0.2483', '0.4822', '0.3572', '0.4807', '-0.349', '-0.845', '-0.279', '-1.24', '-0.7944', '-0.1759', '0.3357', '-0.1658', '-0.3855', '-0.132', '-0.1879', '-0.0959', '-0.1287', '-0.2142', '0.1444', '0.5244', '0.7974', '-0.03625', '0.4595', '-0.2477', '0.6704', '-0.281', '0.0872', '-0.647', '0.7075', '-0.263', '-0.2676', '-0.3616', '1.1045', '-0.11786', '-0.5845', '0.1499', '-0.004463', '0.7236', '0.404', '0.3901', '0.4448', '-0.1143', '0.2365', '0.3474', '0.1718', '0.5513', '0.3098', '0.26', '-0.549', '-0.405', '-0.0862', '-0.6113', '-0.815', '0.6733', '0.2788', '-0.1648', '0.0763', '0.729', '0.03238', '-0.1798', '0.186', '0.11456', '0.4382', '0.8486', '0.5923', '-0.2954', '0.0007763', '-0.4326', '-0.2115', '-0.2808', '0.5874', '0.3193', '0.751', '0.00469', '-0.146', '0.05518', '1.06', '0.1154', '0.01616', '0.006374', '0.1627', '0.1918', '0.614', '-0.12213', '-0.1779', '-0.253', '0.1765', '-0.3018']",,,C536096,333.99,,,
mondo:0000904,complex cortical dysplasia with other brain malformations,"['CDCBM', 'cortical dysplasia, complex, with other brain malformations']",0090131,,,CN228165,"['-0.006516', '0.03047', '-0.001574', '-0.003479', '0.00561', '-0.01633', '0.01164', '0.03802', '-0.02547', '-0.00639', '-0.01634', '0.000871', '-0.001275', '0.001323', '-0.01611', '-0.02492', '0.00249', '-0.009796', '-0.0186', '-0.05597', '0.006386', '-0.00949', '0.03397', '-0.00744', '0.01075', '-0.01752', '-0.00986', '0.00578', '-0.005646', '-0.00565', '0.01654', '-0.01889', '0.02708', '0.02054', '0.02159', '-0.000539', '-0.00927', '-0.008156', '0.00838', '-0.03537', '0.01666', '-0.0223', '0.0048', '-0.00995', '-0.002094', '-0.03427', '-0.011116', '0.01199', '0.00615', '0.001344', '-0.003311', '-0.00794', '-0.00375', '-0.003323', '-0.02217', '0.0009036', '0.01054', '-0.015495', '-0.0242', '0.003294', '0.01909', '0.01457', '-0.0083', '2.706e-05', '-0.01539', '0.001587', '0.04062', '0.01947', '-0.02495', '0.02322', '-0.02428', '0.01061', '0.01038', '-0.01431', '0.001846', '0.01836', '0.00204', '0.01057', '-0.01112', '-0.02115', '-0.01313', '-0.008766', '0.007713', '0.03098', '-0.00784', '0.005524', '0.001374', '0.03668', '0.02496', '0.008026', '0.001074', '0.019', '-0.00927', '0.01488', '0.06177', '0.003595', '0.0273', '-0.0325', '0.006863', '0.005287']",,,,,,,
mondo:0000908,arrhythmogenic right ventricular dysplasia 13,"['arrhythmogenic right ventricular cardiomyopathy caused by mutation in CTNNA3', 'ARVD13', 'ARVC13', 'CTNNA3 arrhythmogenic right ventricular cardiomyopathy', 'arrhythmogenic right ventricular dysplasia, familial, type 13', 'arrhythmogenic right ventricular cardiomyopathy 13', 'arrhythmogenic right ventricular dysplasia type 13', 'familial arrhythmogenic right ventricular dysplasia 13', 'arrhythmogenic right ventricular dysplasia, familial, 13']",0110084,615616,,C3810138,,,,,,,,
mondo:0000909,Bartter disease type 4B,"['Bartter syndrome, type 4b, digenic', 'Bartter syndrome, infantile, with sensorineural deafness', 'BARTS4B', 'Bartter syndrome, type 4B', 'neonatal Bartter syndrome type 4B with sensorineural deafness', 'Bartter syndrome, type 4B, neonatal, with sensorineural deafness']",0110146,613090,,C2751312,,,,,,,,
mondo:0000910,retinitis pigmentosa 6,"['RP 6', 'retinitis pigmentosa 6', 'RP6', 'retinitis pigmentosa type 6', 'retinitis pigmentosa, X-linked recessive, 6']",0110413,312612,,C1839368,,,,C564065,,H35.5,,
mondo:0000912,autosomal recessive nonsyndromic hearing loss 5,"['DFNB5', 'neurosensory nonsyndromic recessive deafness 5', 'autosomal recessive deafness 5', 'autosomal recessive nonsyndromic deafness type 5', 'deafness, autosomal recessive 5', 'autosomal recessive nonsyndromic deafness 5']",0110507,600792,,C1833319,,,,C563444,,,,
mondo:0000913,hereditary spherocytosis type 2,"['hereditary spherocytosis caused by mutation in SPTB', 'SPH2', 'hereditary spherocytosis 2', 'HS2', 'spherocytosis, type 2', 'SPTB hereditary spherocytosis', 'spherocytosis, hereditary, 2', 'hereditary spherocytosis type 2']",0110917,616649,,C2674219,,,,,,,,
mondo:0000914,"cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1","['cerebral arteriopathy with subcortical infarcts and leukoencephalopathy 1', 'CADASIL 1', 'CADASIL type 1', 'cerebral arteriopathy with subcortical infarcts and leukoencephalopathy', 'familial vascular leukoencephalopathy', 'CADASIL', 'CADASIL1', 'cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 1', 'autosomal dominant cerebral arteriopathy with subcortical infarcts and leukoencephalopathy type 1', 'CADASIL syndrome', 'dementia, hereditary multi-infarct type', 'hereditary multi-infarct dementia', 'cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy', 'CASIL']",0111035,125310,136,C0751587,"['0.2335', '0.2866', '-0.3284', '-0.4353', '-0.0881', '-0.0989', '0.4578', '0.5576', '-0.614', '0.0657', '-0.499', '-0.283', '-0.1891', '-0.1624', '0.4285', '-0.1506', '-0.1221', '-0.171', '-0.183', '0.214', '0.1978', '-0.1431', '0.1688', '-0.2117', '0.00868', '-0.5254', '-0.1863', '-0.02237', '0.2008', '-0.3179', '0.6226', '0.06152', '0.424', '-0.441', '0.2064', '0.01772', '-0.2362', '-0.7837', '0.03363', '-0.6562', '0.641', '-0.911', '0.6904', '-0.2913', '0.2019', '0.277', '-0.337', '-0.4487', '0.3413', '0.2625', '0.339', '0.788', '-0.2236', '-0.00975', '0.9155', '0.654', '0.692', '-0.1919', '-0.02657', '0.3684', '0.0618', '0.615', '0.7817', '-0.3984', '-0.04785', '0.4597', '-0.02426', '0.9683', '-0.3196', '0.4287', '-0.364', '-0.14', '-0.0415', '-0.05334', '0.4026', '0.02701', '0.3684', '0.43', '-0.4675', '-0.2184', '-0.1428', '-0.377', '-0.2773', '0.1559', '-0.0481', '0.2913', '0.7246', '0.5435', '0.4507', '-0.07074', '-0.06158', '-0.15', '-0.4983', '0.2242', '0.1987', '0.1947', '0.434', '-0.0676', '-0.271', '-0.152']",C84606,,D046589,,,10065551,
mondo:0000916,intestinal infectious disease,['bacterial enteritis'],100,,,C0178238,,,,,008.8,A00-A09,,
mondo:0000918,endometritis,"['endometrium inflammation', 'uterine infection']",1002,,,C0014179,,C26764,1001312,D004716,,,,
mondo:0000919,ampulla of vater cancer,"['malignant ampulla of Vater neoplasm', 'malignant hepatopancreatic ampulla neoplasm', 'malignant tumor of ampulla of Vater', 'hepatopancreatic ampulla cancer', 'malignant tumour of ampulla of vater', 'malignant tumor of ampulla of vater', 'malignant tumour of the ampulla of Vater', 'malignant tumor of the ampulla of Vater', 'malignant neoplasm of hepatopancreatic ampulla', 'malignant neoplasm of the ampulla of Vater', 'malignant ampulla of Vater tumor', 'malignant ampulla of Vater tumour', 'malignant neoplasm of ampulla of Vater', 'malignant tumour of ampulla of Vater', 'cancer of hepatopancreatic ampulla']",10020,,,C0153454,,C3536,,,156.2,,,
mondo:0000920,duodenum cancer,"['malignant duodenal neoplasm', 'malignant tumor of the duodenum', 'malignant tumour of the duodenum', 'cancer of duodenum', 'malignant duodenum neoplasm', 'malignant tumor of duodenum', 'malignant tumour of duodenum', 'duodenum cancer', 'malignant neoplasm of the duodenum', 'malignant duodenal tumor', 'malignant duodenal tumour', 'malignant neoplasm of duodenum', 'duodenal cancer']",10021,,,,,C9328,,D004379,152.0,,,
mondo:0000921,ampulla of vater neoplasm,"['tumor of the ampulla of Vater', 'hepatopancreatic ampulla tumour', 'ampulla of Vater tumour', 'neoplasm of hepatopancreatic ampulla', 'hepatopancreatic ampulla neoplasm (disease)', 'neoplasm of ampulla of Vater', 'tumour of hepatopancreatic ampulla', 'tumour of ampulla of Vater', 'tumor of ampulla of Vater', 'tumour of the ampulla of Vater', 'neoplasm of the ampulla of Vater', 'ampulla of Vater tumor', 'tumor of hepatopancreatic ampulla', 'AMPULLAOFVATER', 'hepatopancreatic ampulla tumor']",10022,,,C0345916,,C4443,,,,,,
mondo:0000922,pelvic inflammatory disease,"['PID, pelvic inflammatory disease', 'disease (PID), pelvic inflammatory', 'pelvic inflammatory disease, (PID)', 'inflammatory disease (PID), pelvic', 'PID', 'pelvic infection', 'pelvic inflammatory disease']",1003,,,C0242172,,C3889,1001388,D000292,614.9,N70-N77,,
mondo:0000923,interstitial emphysema,"['pulmonary interstitial emphysema', 'interstitial emphysema of lung', 'pie']",10030,,,C1370824,,C34571,,,518.1,J98.2,,
mondo:0000924,compensatory emphysema,,10031,,,C0155918,,,,,518.2,J98.3,,
mondo:0000925,hyperlucent lung,,10032,,,C0524799,,,,D019568,,,,
mondo:0000926,eye accommodation disease,,10034,,,C0152198,,,,,367.5,,,
mondo:0000927,asymptomatic neurosyphilis,,10035,,,C0153167,,,,,094.3,A52.2,,
mondo:0000928,eyelid melanoma,"['eyelid melanoma (disease)', 'eyelid melanoma', 'malignant eyelid melanoma', 'melanoma of the eyelid', 'melanoma of eyelid', 'malignant melanoma of the eyelid', 'malignant melanoma of eyelid']",10040,,,C0339116,,C4358,,,172.1,,,
mondo:0000929,balloon cell malignant melanoma,"['balloon cell malignant melanoma of skin', 'balloon cell cutaneous (skin) melanoma', 'balloon cell skin melanoma', 'balloon cell melanoma', 'balloon cell malignant skin melanoma', 'balloon cell malignant melanoma of the skin']",10044,,,C0334426,,C4227,,,,,,
mondo:0000930,nodular malignant melanoma,"['nodular melanoma (morphologic abnormality)', 'nodular malignant melanoma of the skin', 'nodular cutaneous (skin) melanoma', 'nodular malignant melanoma of skin', 'nodular malignant skin melanoma', 'nodular melanoma']",10047,,,C0334424,,C4225,0008515,,,,,
mondo:0000931,endometrial disorder,"['endometrium disease', 'endometrium disease or disorder', 'disease of endometrium', 'disorder of endometrium']",1005,,,,,C3504,,,,,,
mondo:0000933,subglottis neoplasm,"['subglottis tumour', 'neoplasm of the subglottis', 'subglottic neoplasm', 'tumour of the subglottis', 'subglottic tumour', 'subglottis neoplasm (disease)', 'tumor of subglottis', 'subglottis tumor', 'tumor of the subglottis', 'tumour of subglottis', 'subglottic tumor', 'subglottis neoplasm', 'neoplasm of subglottis']",10069,,,C0345746,,C4426,,,,,,
mondo:0000934,laryngeal leiomyoma,"['leiomyoma of the larynx', 'laryngeal leiomyoma', 'leiomyoma of larynx', 'larynx leiomyoma']",10070,,,C1334370,,C6027,,,,,,
mondo:0000935,larynx squamous papilloma,"['papilloma of the larynx', 'squamous papilloma of larynx', 'larynx papilloma', 'papilloma of larynx', 'laryngeal papilloma', 'squamous papilloma of the larynx', 'larynx squamous papilloma']",10071,,,C0240164,,C7742,,,,,,
mondo:0000936,syphilitic meningitis,"['meningeal syphilis', 'meningitis, syphilitic', 'Treponema caused infectious meningitis', 'syphilitic aseptic meningitis']",10073,,,C0153166,,,,C536775,094.2,,,
mondo:0000937,syphilitic encephalitis,['Treponema caused encephalitis'],10081,,,C0153168,,,,,094.81,,,
mondo:0000938,gastric leiomyoma,"['stomach leiomyoma', 'gastric leiomyoma', 'leiomyoma of stomach', 'leiomyoma of the stomach']",10087,,,C0238440,,C3876,,,,,,
mondo:0000939,intracranial abscess,,10095,,,C0021874,,C34734,,,324.0,,,
mondo:0000940,trypanosomiasis,"['Trypanosoma caused disease or disorder', 'Trypanosomiases']",10113,,,C0041227,,,,D014352,086.9,B56,,
mondo:0000941,eyelid degenerative disorder,"['eyelid neurodegenerative disease', 'neurodegenerative disease of eyelid']",10120,,,C0155209,,,,,374.50,,,
mondo:0000942,corneal disorder,"['corneal disorder', 'disease of cornea', 'corneal disease', 'disorder of cornea', 'cornea disease', 'cornea disease or disorder']",10124,,,C0010034,,C26731,,D003316,371.9,,,
mondo:0000943,acute hydrops keratoconus,"['acute hydrops of cornea', 'acute corneal hydrops', 'keratoconus, acute hydrops']",10125,,,C0339286,,,,,371.62,,,
mondo:0000944,cerebral artery occlusion,,10127,,,,,,,,434.91,,,
mondo:0000945,venous insufficiency,"['venous insufficiency', 'venous insufficiency (disease)', 'peripheral venous insufficiency']",10128,,,C0042485,,,,D014689,459.81,,,0005293
mondo:0000946,psychologic vaginismus,"['functional vaginismus', 'psychogenic vaginismus', 'non-organic vaginismus']",10131,,,,,,,,306.51,,,
mondo:0000947,psychosexual disorder,,10132,,,,,,,,302.9,,,
mondo:0000948,xerophthalmia,['conjunctival xerosis'],10138,,,C3665609,,C34503,,D014985,375.15,,,
mondo:0000949,conjunctival degeneration,,10139,,,C0155160,,,,,372.50,,,
mondo:0000950,asthenopia,['accommodative strain'],10141,,,C0004095,,,,D001248,,,,
mondo:0000951,thymus lymphoma,"['lymphoma of Thymus', 'Thymus lymphoma', 'thymus lymphoma', 'primary thymic lymphoma', 'thymic lymphoma', 'lymphoma of the Thymus']",10146,,,C1336745,,C6451,1000054,,,,,
mondo:0000952,cancer of long bone of lower limb,"['malignant neoplasm of long bones of leg', 'hindlimb long bone cancer', 'malignant neoplasm of hindlimb long bone', 'cancer of hindlimb long bone', 'malignant hindlimb long bone neoplasm', 'long bones of lower limb cancer']",10149,,,C3265932,,,,,170.7,C40.2,,
mondo:0000953,cancer of short bone of lower limb,"['malignant neoplasm of short bones of leg', 'malignant neoplasm of short bone of lower limb']",10151,,,C0153518,,,,,170.8,C40.3,,
mondo:0000954,Meckel diverticulum cancer,"['Meckel diverticulum cancer', 'Meckel^s diverticulum cancer', 'cancer of Meckel^s diverticulum', 'malignant neoplasm of Meckel^s diverticulum', 'malignant Meckel^s diverticulum neoplasm']",10152,,,C0153429,,,,,152.3,,,
mondo:0000955,ileum cancer,"['cancer of ileum', 'malignant neoplasm of ileum', 'ileum cancer', 'malignant ileum neoplasm']",10153,,,,,,,,152.2,,,
mondo:0000956,small intestine cancer,"['malignant tumor of small intestine', 'cancer of small intestine', 'malignant tumour of the small intestine', 'malignant tumor of small bowel', 'malignant small intestine tumor', 'malignant small intestine neoplasm', 'malignant tumour of the small bowel', 'small intestine cancer', 'malignant neoplasm of the small bowel', 'malignant neoplasm of the small intestine', 'malignant tumor of the small bowel', 'malignant tumor of the small intestine', 'small bowel tumors', 'malignant tumour of small intestine', 'malignant small bowel tumour', 'malignant neoplasm of small bowel', 'malignant neoplasms of the small intestine', 'malignant small bowel neoplasm', 'small bowel tumours', 'malignant neoplasm of small intestine', 'malignant tumour of small bowel', 'malignant small intestinal neoplasm', 'malignant small intestine tumour', 'malignant small bowel tumor']",10154,,,C0153425,,C7523,,,152.9,,,
mondo:0000957,lacrimal passage granuloma,['granuloma of lacrimal passages'],10174,,,C0155253,,,,,375.81,,,
mondo:0000958,neuroretinitis,"['focal retinitis and retinochoroiditis, juxtapapillary', 'Juxtapapillary focal retinitis and retinochoroiditis', 'papilloretinitis']",10176,,,C0154874,,,,D012173,363.05,,,
mondo:0000959,malignant hypertensive renal disease,,10177,,,C0155593,,,,,403.00,,,
mondo:0000960,diabetic peripheral angiopathy,"['diabetic angiopathy', 'diabetic vascular disorder']",11713,,,C0011875,,C35610,1000896,D003925,443.81,,,
mondo:0000961,endobronchial lipoma,['endobronchial lipoma'],10183,,,C0852937,,C5063,,,,,,
mondo:0000962,spindle cell lipoma,"['spindle cell lipoma', 'spindle cell lipoma (morphologic abnormality)']",10184,,,C0334474,,C4254,,,,,,
mondo:0000963,esophageal lipoma,"['oesophagus lipoma', 'lipoma of oesophagus', 'lipoma of the oesophagus', 'lipoma of esophagus', 'lipoma of the esophagus', 'esophagus lipoma', 'esophageal lipoma']",10187,,,C1333455,,C5701,,,,,,
mondo:0000964,skin lipoma,"['cutaneous lipomatous tumour', 'lipoma of face', 'cutaneous lipoma', 'lipoma of zone of skin', 'lipoma of skin', 'zone of skin lipoma', 'skin lipoma', 'lipoma of the skin', 'cutaneous lipomatous tumor']",10188,,,,,C4616,,,214.1,,,
mondo:0000965,liver lipoma,"['hepatic lipoma', 'lipoma of liver', 'liver lipoma', 'lipoma of the liver']",10190,,,C1333970,,C5750,,,,,,
mondo:0000966,pleomorphic lipoma,"['pleomorphic lipoma', 'pleomorphic lipoma (morphologic abnormality)']",10192,,,C0205823,,C3703,,,,,,
mondo:0000967,conventional lipoma,"['classic type lipoma', 'conventional lipoma']",10193,,,C1333059,,C27530,,,,,,
mondo:0000968,kidney lipoma,"['lipoma of the kidney', 'kidney lipoma', 'renal lipoma', 'lipoma of kidney']",10194,,,C1335744,,C5101,,,,,,
mondo:0000969,pleural lipoma,"['lipoma of the pleura', 'pleura lipoma', 'pleural lipoma', 'lipoma of pleura']",10195,,,C1335434,,C6644,,,,,,
mondo:0000970,breast lipoma,"['lipoma of the breast', 'breast lipoma', 'lipoma of breast']",10199,,,C0349565,,C4647,,,214.1,,,
mondo:0000971,chest wall lipoma,"['lipoma of the chest wall', 'chest wall lipoma', 'lipoma of chest wall']",10200,,,C1332932,,C6719,,,214.8,,,
mondo:0000972,gallbladder lipoma,"['lipoma of the gallbladder', 'gall bladder lipoma', 'lipoma of gall bladder', 'lipoma of gallbladder', 'gallbladder lipoma']",10201,,,C1333747,,C5835,,,,,,
mondo:0000973,external ear lipoma,"['external Ear lipoma', 'lipoma of the external ear', 'lipoma of the external auditory meatus', 'lipoma of external auditory meatus', 'external ear lipoma', 'lipoma of external Ear', 'lipoma of the external Ear', 'external auditory meatus lipoma']",10203,,,C0347423,,C4618,,,215.0,,,
mondo:0000974,axillary lipoma,"['axillary lipoma', 'lipoma of axilla', 'axilla lipoma']",10205,,,C0347429,,C35419,,,214.8,,,
mondo:0000975,lipoma of spermatic cord,"['spermatic cord lipoma', 'lipoma of the spermatic cord', 'lipoma of spermatic cord']",10206,,,C0153972,,C3606,,,214.4,,,
mondo:0000976,paratesticular lipoma,['paratesticular lipoma'],10207,,,C1335348,,C6384,,,,,,
mondo:0000977,chondroid lipoma,,10208,,,C1266131,,C6503,,,,,,
mondo:0000978,extrahepatic bile duct lipoma,"['lipoma of the extrahepatic bile duct', 'extrahepatic bile duct lipoma', 'lipoma of extrahepatic bile duct']",10209,,,C1333509,,C5854,,,,,,
mondo:0000979,pinta disease,"['Tina', 'Azul', 'endemic treponematosis caused by Treponema carateum', 'Mal del pinto', 'Empeines', 'pinta', 'Carate', 'Lota']",1022,,,C0031946,,C85011,1001396,D010874,103.9,,,
mondo:0000980,aortic atherosclerosis,"['aorta atherosclerosis', 'atherosclerosis of aorta', 'aortic atherosclerosis (disease)', 'aortic atherosclerosis']",10230,,,C0155733,,,,,440.0,,,0012397
mondo:0000981,Histoplasma pericarditis,"['acute Histoplasma pericarditis', 'Histoplasma caused pericarditis (disease)']",10234,,,C0153279,,,,,115.93,,,
mondo:0000983,exhibitionism,,10236,,,,,C94352,,D005084,302.4,F65.2,,
mondo:0000984,thalassemia,"['sickle-cell thalassemia without crisis', 'thalassemia Hb-S disease with crisis', 'thalassemia Hb-S disease without crisis', 'sickle-cell thalassemia with crisis']",10241,,,C0039730,,C35069,1001996,D013789,282.49,D56,,
mondo:0000986,pleurisy,"['pleura inflammation', 'pleuritis']",10247,,,C0032231,,C26860,1001825,D010998,511.8,R09.1,,
mondo:0000987,cholesterolosis of gallbladder,['strawberry gallbladder'],10254,,,C0152456,,,,,575.6,K82.4,,
mondo:0000988,discharging ear,,10261,,,,,,,,388.60,,,
mondo:0000989,mumps infectious disease,"['mumps', 'epidemic parotitis', 'Mumps virus caused disease or disorder']",10264,,,C0026780,,C29888,0007383,D019351,072,B26,,
mondo:0000990,acute subendocardial myocardial infarction,"['subendocardial infarction acute myocardial infarction', 'subendocardial myocardial infarction, acute']",10266,,,C0264710,,,,,410.72,,,
mondo:0000992,heart conduction disease,['heart rhythm disease'],10273,,,,,,,,426.6,,,
mondo:0000993,prostate squamous cell carcinoma,"['PRSC', 'squamous cell carcinoma of the prostate', 'prostate squamous cell carcinoma', 'prostate gland squamous cell carcinoma', 'squamous cell carcinoma of prostate']",10287,,,C1302530,,C5536,,,,,,
mondo:0000994,malignant prostate phyllodes tumor,"['malignant phyllodes tumor of prostate', 'malignant phyllodes tumor of the prostate', 'prostate malignant phyllodes tumor', 'malignant phyllodes neoplasm of the prostate', 'prostate malignant phyllodes tumour', 'malignant phyllodes tumour of the prostate', 'malignant phyllodes tumour of prostate', 'malignant prostate phyllodes neoplasm', 'malignant phyllodes neoplasm of prostate', 'malignant prostate phyllodes tumor']",10289,,,C1334615,,C5531,,,,,,
mondo:0000995,familial periodic paralysis,"['periodic paralyzes, familial', 'periodic paralysis, familial', 'familial periodic paralysis', 'familial periodic paralyzes', 'periodic paralysis, normokalemic', 'paralyzes, normokalemic periodic', 'normokalemic periodic paralysis', 'paralysis, normokalemic periodic', 'normokalemic periodic paralyzes', 'paralysis, familial periodic', 'genetic periodic paralysis', 'normokalemic periodic paralyses', 'periodic paralyzes, normokalemic', 'familial periodic paralyses', 'hereditary periodic paralysis (disease)']",1029,,371433,,,C84709,,D010245,,,,
mondo:0000996,prostate lymphoma,"['lymphoma of the prostate', 'lymphoma of prostate', 'prostate lymphoma', 'lymphoma of prostate gland', 'primary prostate lymphoma', 'prostate gland lymphoma']",10290,,,C1335512,,C5533,,,,,,
mondo:0000997,monocular esotropia,,10293,,,C0152204,,,,,378.01,,,
mondo:0001000,mixed mineral dust pneumoconiosis,"['mineral dust pneumoconiosis', 'mixed mineral dust pneumoconiosis', 'mineral duct pneumoconiosis']",10319,,,C0340184,,C27559,,,503,,,
mondo:0001001,baritosis,"['deposition of barium in the lungs', 'inhalation of barytes']",10321,,,C0340177,,C34410,,C537080,503,,,
mondo:0001003,pneumoconiosis due to talc,['talc pneumoconiosis'],10329,,,C0238377,,C27026,,,502,,,
mondo:0001004,slate pneumoconiosis,['Schistosis'],10330,,,C0340186,,C35397,,,502,,,
mondo:0001005,kaolin pneumoconiosis,"['Kaolinosis', 'simple kaolinosis']",10331,,,C0264435,,C35315,,,502,,,
mondo:0001006,glaucomatous atrophy of optic disk,"['glaucomatous atrophy [cupping] of optic disk', 'glaucomatous atrophy [cupping] of optic disc']",10337,,,C0271342,,,,,377.14,,,
mondo:0001007,chronic meningitis,"['meningitis (disease), chronic']",10341,,,C0154653,,,,,322.2,G03.1,,
mondo:0001008,blepharophimosis,"['blepharophimosis (disease)', 'blepharophimosis']",10348,,,,,,,D016569,374.46,,,0000581
mondo:0001009,solitary cyst of breast,"['solitary cyst of the breast', 'solitary cyst of breast']",10349,,,,,,,,610.0,N60.0,,
mondo:0001011,breast cyst,['cyst of the breast'],10350,,,,,,1000848,D047688,,,,
mondo:0001014,chronic leukemia,"['leukemia (disease), chronic', 'leukaemia (disease), chronic', 'CLL', 'chronic leukaemia (disease)', 'adult chronic leukaemia', 'chronic leukemia', 'adult chronic leukemia', 'CML']",1036,,,C1279296,,C3483,,,208.10,,,
mondo:0001015,eosinophilic meningitis,,10361,,,C0154652,,C128374,,,322.1,,,
mondo:0001016,epididymis cancer,"['malignant tumor of the epididymis', 'malignant tumour of epididymis', 'cancer of epididymis', 'malignant epididymal neoplasm', 'malignant tumour of the epididymis', 'epididymis cancer', 'malignant epididymal tumor', 'malignant neoplasm of epididymis', 'malignant neoplasm of the epididymis', 'malignant epididymis neoplasm', 'malignant tumor of epididymis', 'malignant epididymal tumour']",10366,,,C0153602,,C3558,,,187.5,,,
mondo:0001017,epididymal adenocarcinoma,"['epididymis adenocarcinoma', 'epididymal adenocarcinoma', 'adenocarcinoma of the epididymis']",10368,,,C1510784,,C39957,,,,,,
mondo:0001019,suppression amblyopia,['strabismic amblyopia'],10375,,,C0750903,,,,,368.01,,,
mondo:0001020,amblyopia,"['amblyopia (disease)', 'lazy eye', 'amblyopia']",10376,,,C0002418,,C118764,,D000550,368.00,,,0000646
mondo:0001021,ametropic amblyopia,['refractive amblyopia'],10377,,,C0152190,,,,,368.03,,,
mondo:0001022,disuse amblyopia,['deprivation amblyopia'],10378,,,C0152189,,,,,368.02,,,
mondo:0001023,prolymphocytic leukemia,"['PLL', 'prolymphocytic leukaemia (B or T-cell)', 'prolymphocytic leukemia (B or T-cell)', 'prolymphocytic leukemia (B or T)', 'prolymphocytic leukemia', 'prolymphocytic leukaemia (B or T)']",1039,,,C0023486,,C3181,,D015463,204.80,,,
mondo:0001024,pneumonic plague,"['primary pneumonic plague', 'secondary pneumonic plague']",10398,,,C0524688,,,,,020.5,A20.2,,
mondo:0001025,seminal vesicle chronic gonorrhea,"['gonococcal seminal vesiculitis, chronic', 'chronic gonococcal seminal vesiculitis']",10399,,,C0153205,,,,,098.34,,,
mondo:0001027,gonococcal seminal vesiculitis,"['seminal vesicle gonorrhea', 'seminal vesicle gonorrhoea', 'gonococcal seminal vesiculitis (acute)', 'gonorrhea of seminal vesicle', 'gonorrhoea of seminal vesicle']",10400,,,C0578661,,,,,,,,
mondo:0001028,acute pericementitis,"['periodontitis, acute', 'acute periodontitis']",10423,,,C0001342,,C34354,,,523.33,,,
mondo:0001029,Klippel-Feil syndrome,"['Klippel Feil syndrome', 'Klippel-Feil deformity, deafness and facial asymmetry', 'Klippel-Feil Sequence', 'cervical vertebral fusion', 'Klippel-Feil and Turner syndrome', 'autosomal dominant Klippel-Feil syndrome', 'congenital dystrophia brevicollis', 'congenital synostosis of cervical vertebrae']",10426,,,,,C98967,,D007714,756.16,Q76.1,,
mondo:0001030,"keratoconus, stable condition",['stable condition keratoconus'],10428,,,C0155131,,,,,371.61,,,
mondo:0001031,purulent acute otitis media,"['suppurative otitis media, acute', 'acute suppurative otitis media']",10435,,,C0271431,,,,,382.02,,,
mondo:0001032,Mooren ulcer,['Mooren^s ulcer'],10439,,519408,C0155072,,,,,370.07,,,
mondo:0001033,mycotic corneal ulcer,,10440,,,C0155071,,,,,370.05,,,
mondo:0001034,marginal corneal ulcer,,10441,,,C0155067,,,,,370.01,,,
mondo:0001035,hypopyon ulcer,,10442,,,C0155070,,,,,370.04,,,
mondo:0001036,hypopyon,,10443,,,C0020641,,C50593,,,364.05,,,
mondo:0001037,ring corneal ulcer,,10444,,,C0155068,,,,,370.02,,,
mondo:0001038,perforated corneal ulcer,,10445,,,C0151844,,,,,370.06,,,
mondo:0001039,tonsillitis,"['throat infection - tonsillitis', 'tonsilitis', 'chronic tonsillitis', 'tonsil inflammation']",10456,,,C0149517,,C116006,,D014069,474.00,J35.01,,
mondo:0001040,nasopharyngitis,"['nasopharynx inflammation', 'chronic nasopharyngitis']",10460,,,C0155826,,C34837,,D009304,472.2,,,
mondo:0001041,dentin caries,"['dental caries of dentine', 'dentine dental caries', 'compound dental caries', 'dental caries extending into dentine']",10461,,,C0266846,,,,,521.02,,,
mondo:0001042,patellar tendinitis,"['patella tendinitis', 'tendinitis of patella', 'patellar tendonitis']",10471,,,C0158317,,,,,726.64,M76.5,,
mondo:0001044,esophageal atresia,"['congenital esophageal atresia', 'congenital imperforate esophagus', 'imperforate oesophagus', 'esophageal atresia', 'imperforate esophagus', 'oesophageal atresia', 'esophageal atresia (disease)', 'congenital atresia of esophagus', 'congenital atresia of oesophagus', 'congenital imperforate oesophagus']",10485,,,,,C87072,,D004933,750.3,,,0002032
mondo:0001045,intestinal atresia,"['intestinal atresia', 'atresia of the intestine', 'congenital intestinal atresia', 'intestinal atresia (disease)']",10486,,,C0021828,,C84790,,D007409,,,,0011100
mondo:0001046,imperforate anus,"['anal atresia', 'anal stenosis', 'congenital atresia of anus', 'congenital or infantile occlusion of anus', 'anus, imperforate', 'anorectal malformations', 'imperforate anus']",10488,301800,,,,C84784,,D001006,,,,
mondo:0001048,orbital granuloma,,10499,,,C0155262,,,,,376.11,,,
mondo:0001049,Dressler syndrome,"['Dressler^s syndrome', 'Dressler syndrome', 'postmyocardial infarction syndrome']",10507,,,C0152107,,,,,411.0,I24.1,,
mondo:0001050,malignant otitis externa,,10516,,,C0155395,,,,,380.14,H60.2,,
mondo:0001051,acute otitis externa,"['acute swimmers^ ear', 'acute otitis externa, diffuse', 'otitis externa, acute', 'beach ear', 'acute swimmer^s ear', 'acute bacterial inflammation of external ear', 'acute otitis externa', 'tank ear']",10518,,,C0149948,,,,,380.12,,,
mondo:0001052,chronic fungal otitis externa,"['chronic mycotic otitis externa', 'otomycosis, chronic', 'chronic otomycosis']",10519,,,C0155396,,,,,380.15,,,
mondo:0001053,acute infection of pinna,,10520,,,C0155392,,,,,380.11,,,
mondo:0001054,double pterygium,,10525,,,C0155157,,,,,372.44,,,
mondo:0001055,conjunctival pterygium,['web eye'],10526,,,,,,,,,,,
mondo:0001056,gastric cancer,"['malignant neoplasm of the stomach', 'malignant tumour of lesser curve of stomach', 'malignant tumour of greater curve of stomach', 'malignant tumour of body of stomach', 'gastric cancer, intestinal', 'gastric neoplasm', 'malignant neoplasm of stomach', 'cancer of stomach', 'gastric cancer risk after h. pylori infection', 'ca greater curvature of stomach', 'stomach cancer', 'malignant neoplasm of lesser curve of stomach', 'Ca body - stomach', 'malignant tumor of greater curve of stomach', 'gastric cancer, somatic', 'malignant tumour of stomach', 'malignant tumor of body of stomach', 'malignant tumor of stomach', 'Ca lesser curvature - stomach', 'malignant gastric tumor', 'malignant neoplasm of body of stomach', 'malignant gastric neoplasm', 'malignant stomach neoplasm', 'malignant gastric tumour', 'malignant tumor of lesser curve of stomach', 'malignant tumour of the stomach', 'gastric cancer', 'malignant tumor of the stomach']",10534,613659,63443,,"['0.01685', '0.01955', '0.004375', '-0.03467', '0.002022', '-0.04492', '0.02228', '0.04434', '-0.04468', '-0.02145', '0.002556', '0.009964', '-0.005646', '0.02002', '-0.03156', '-0.03778', '-0.00933', '-0.01419', '-0.0057', '-0.11066', '-0.0048', '-0.0444', '0.02745', '-0.0509', '0.05057', '-0.029', '-0.005577', '-0.005447', '-0.007084', '-0.06445', '0.04697', '-0.01158', '0.0612', '-0.01073', '0.00797', '-0.004913', '-0.0241', '-0.009026', '-0.006134', '-0.02979', '0.001991', '-0.04758', '0.02931', '-0.04358', '0.01729', '-0.03146', '-0.01361', '0.03378', '0.01212', '0.0278', '-0.00793', '0.01085', '0.02278', '0.0197', '-0.046', '-0.007088', '0.03625', '-0.0206', '-0.0741', '-0.003214', '0.0435', '0.010475', '0.003435', '0.00328', '-0.003042', '0.0334', '0.0644', '0.04022', '-0.04044', '0.05032', '-0.013245', '0.004295', '-0.003998', '-0.0311', '0.03592', '0.02415', '-0.00078', '-0.03387', '-0.02377', '-0.026', '-0.03372', '-0.008255', '-0.01842', '0.0398', '-0.06055', '-0.00461', '0.03099', '0.01569', '0.069', '-0.00843', '-0.00985', '0.0644', '0.002455', '-0.003052', '0.10144', '0.0251', '0.0497', '-0.04077', '-0.04178', '0.010574']",C9331,,,151.9,C16,,
mondo:0001057,malignant gastric granular cell tumor,"['malignant granular cell neoplasm of the stomach', 'malignant granular cell tumor of stomach', 'malignant granular cell stomach tumour', 'malignant gastric granular cell neoplasm', 'malignant granular cell stomach neoplasm', 'malignant granular cell tumour of the stomach', 'malignant gastric granular cell tumor', 'malignant granular cell neoplasm of stomach', 'malignant granular cell tumor of the stomach', 'malignant granular cell tumour of stomach', 'malignant granular cell stomach tumor']",10536,,,C1334585,,C5484,,,,,,
mondo:0001059,gastric lymphoma,"['gastric lymphoma', 'stomach lymphoma', 'lymphoma of the stomach', 'lymphoma of stomach', 'primary gastric lymphoma']",10540,,,C0349532,,C4636,,,202.83,,,
mondo:0001060,microinvasive gastric cancer,"['early gastric cancer', 'superficial spreading gastric cancer', 'superficial gastric cancer', 'EGC', 'surface gastric cancer']",10541,,,C0349530,,C27131,,,,,,
mondo:0001061,pylorus cancer,"['pylorus cancer', 'malignant neoplasm of pylorus', 'malignant tumour of pylorus', 'cancer of pylorus', 'malignant neoplasm of pylorus of stomach', 'malignant tumor of pylorus', 'malignant neoplasm of Prepylorus', 'malignant pylorus neoplasm', 'Ca pylorus - stomach']",10544,,,C0153418,,,,,151.1,,,
mondo:0001062,pyloric antrum cancer,"['malignant tumour of pyloric antrum', 'malignant tumor of pyloric antrum', 'malignant pyloric antrum neoplasm', 'malignant neoplasm of antrum of stomach', 'cancer of pyloric antrum', 'pyloric antrum cancer', 'malignant neoplasm of pyloric antrum']",10547,,,C0153419,,,,,151.2,,,
mondo:0001063,cardia cancer,"['malignant neoplasm of cardia of stomach', 'malignant cardia of stomach neoplasm', 'cancer of cardia of stomach', 'Ca cardia - stomach', 'cardia of stomach cancer']",10548,,,C0153417,,,,,151.0,,,
mondo:0001064,acute eustachian salpingitis,"['otosalpingitis, acute', 'acute eustachian tube salpingitis', 'acute otosalpingitis']",10550,,,C0155429,,,,,381.51,,,
mondo:0001065,supine hypotensive syndrome,"['postpartum maternal hypotension syndrome', 'antepartum maternal hypotension syndrome']",10556,,,,,,,,669.20,,,0008071
mondo:0001066,late yaws,"['nodular late yaws', 'gummata of yaws', 'multiple papillomata due to yaws and wet crab yaws', 'gummatous frambeside', 'gummata and ulcers due to yaws', 'ulcers of yaws', 'yaws gummata and ulcers']",10567,,,C1517744,,C41354,,,102.4,A66.4,,
mondo:0001067,early yaws,"['initial lesions of yaws', 'chancre of yaws', 'bone and joint yaws lesion', 'primary frambesia', 'frambesia, initial or primary', 'bone and joint lesions due to yaws', 'initial frambesial ulcer']",10568,,,C0275998,,C41352,,,102.6,,,
mondo:0001068,osteomalacia,"['osteomalacia (disease)', 'osteomalacia']",10573,,,,,C26838,1002027,D010018,268.2,,,0002749
mondo:0001071,intellectual disability,"['intellectual disabilities', 'mental retardation']",1059,,319658,,"['-0.04974', '0.287', '0.0803', '0.02061', '-0.1404', '-0.1398', '0.3374', '0.4458', '-0.4565', '-0.228', '-0.01528', '0.17', '0.1361', '0.2417', '0.1261', '-0.0644', '0.1414', '-0.1412', '-0.2312', '-0.5986', '0.0546', '0.1812', '0.1378', '-0.03363', '0.1925', '-0.0865', '-0.1473', '0.02368', '-0.3418', '0.151', '0.2603', '-0.1836', '0.1436', '0.2607', '-0.1772', '-0.02899', '0.1698', '-0.06555', '-0.3918', '-0.363', '0.306', '-0.1197', '-0.1741', '0.1333', '-0.1862', '-0.405', '0.2842', '-0.01659', '0.2634', '0.3792', '-0.1024', '0.006447', '-0.274', '0.1289', '0.1467', '0.0419', '-0.03806', '-0.02321', '-0.1128', '0.1747', '-0.1217', '0.1016', '-0.02599', '0.2637', '0.08203', '0.4326', '0.1464', '0.4165', '-0.334', '0.1398', '-0.3535', '-8.77e-05', '0.068', '-0.1451', '0.2568', '0.1093', '0.1277', '0.04672', '-0.618', '-0.2017', '0.253', '0.141', '-0.2634', '0.1569', '0.11383', '0.02205', '-0.004364', '0.01926', '0.3586', '0.1201', '0.0767', '0.47', '-0.195', '0.0821', '-0.1411', '0.1296', '0.2384', '-0.1792', '0.15', '0.1694']",C97250,0003847,D008607,319,F70-F79,,
mondo:0001072,mild pre-eclampsia,,10590,,,,,,,,642.44,,,
mondo:0001073,idiopathic progressive polyneuropathy,,10593,,,C0154756,,,,,356.4,,,
mondo:0001074,chronic tic disorder,"['tic disorder, chronic', 'chronic motor or vocal tic disorder']",10600,,,,,C116768,,,307.22,F95.1,,
mondo:0001075,steatorrhea,"['steatorrhea (disease)', 'fatty stool', 'steatorrhea', 'fatty stool (finding)']",10602,,,,,C86917,,D045602,,,,0002570
mondo:0001076,glucose intolerance,"['glucose: [intolerance] or [malabsorption]', 'glucose: intolerance', 'glucose: malabsorption', 'malabsorption of glucose']",10603,,,C0271650,,C34646,,D018149,271.3,,,
mondo:0001078,tropical sprue,"['tropical steatorrhea', 'post-infective tropical malabsorption', 'tropical enteropathy', 'sprue - tropical', 'idiopathic tropical malabsorption syndrome']",10607,,,C0038054,,C45428,,D013182,579.1,K90.1,,
mondo:0001079,pancreatic steatorrhea,['pancreatic steatorrhoea'],10610,,,C0152166,,,,,579.4,K90.3,,
mondo:0001080,acute gonococcal cervicitis,"['gonococcal cervicitis, acute', 'gonococcal cervicitis (acute)', 'acute gonorrhea of cervix', 'acute gonorrhoea of cervix']",10615,,,C0153195,,,,,098.15,,,
mondo:0001081,acute cervicitis,"['cervicitis (disease), acute']",10616,,,C0269061,,C27056,,,,,,
mondo:0001082,lymph node cancer,"['lymph node neoplasm', 'malignant lymph node neoplasm', 'cancer of lymph node', 'lymph node cancer', 'malignant neoplasm of lymph node']",10619,,,,,C35812,,,239.89,,,
mondo:0001083,Fanconi renotubular syndrome,"['toni-debre-Fanconi syndrome', 'De toni-debre-Fanconi syndrome', 'De toni-Fanconi syndrome', 'Lignac-Fanconi syndrome', 'deToni Fanconi syndrome', 'infantile nephropathic cystinosis', 'Fanconi^s syndrome', 'Fanconi-de-toni syndrome', 'congenital Fanconi syndrome', 'Fanconi-de toni syndrome', 'Fanconi syndrome', 'adult Fanconi syndrome']",1062,,,C0015624,,C3034,,D005198,,,,
mondo:0001084,primary optic atrophy,,10627,,,C0155291,,,,,377.11,,,
mondo:0001085,interstitial nephritis,"['Tubulointerstitial nephritis', 'renal tubulo-interstitial disease']",1063,,,C0041349,,C26834,,D009395,583.89,N10-N16,,
mondo:0001086,partial optic atrophy,,10631,,,C0155295,,,,,377.15,,,
mondo:0001087,schizotypal personality disorder,,10646,,,,,C92632,,D012569,301.22,,,
mondo:0001088,acute inferoposterior infarction,,10648,,,C0340304,,,,,410.32,,,
mondo:0001089,acute inferolateral myocardial infarction,,10649,,,C0340308,,,,,410.22,,,
mondo:0001090,acute anterolateral myocardial infarction,"['anterolateral myocardial infarction, acute']",10651,,,C0155627,,,,,410.02,,,
mondo:0001091,lipoma of colon,"['colonic lipoma', 'lipoma of colon', 'lipoma of the colon', 'colon lipoma']",10655,,,C0940607,,C5493,,,,,,
mondo:0001092,colon leiomyoma,"['leiomyoma of colon', 'leiomyoma of the colon', 'colonic leiomyoma', 'colon leiomyoma']",10656,,,C1333092,,C5492,,,,,,
mondo:0001093,colonic lymphangioma,"['lymphangioma of colon', 'colon lymphangioma', 'lymphangioma of the colon', 'colonic lymphangioma']",10657,,,C1333094,,C5500,,,,,,
mondo:0001094,residual stage of open angle glaucoma,"['open-angle glaucoma residual stage', 'residual stage of open angle glaucoma']",1066,,,C0154944,,,,,365.15,,,
mondo:0001095,mediastinum neuroblastoma,"['neuroblastoma of the mediastinum', 'mediastinum neuroblastoma', 'mediastinal neuroblastoma', 'neuroblastoma of mediastinum']",10660,,,C1334673,,C6628,1000367,,,,,
mondo:0001096,mediastinum ganglioneuroblastoma,"['ganglioneuroblastoma of mediastinum', 'mediastinal ganglioneuroblastoma', 'mediastinum ganglioneuroblastoma (disease)', 'ganglioneuroblastoma of the mediastinum']",10661,,,C1334653,,C6627,,,,,,
mondo:0001098,separation anxiety disorder,,10685,,,,,C35014,1001916,D001010,,,,
mondo:0001099,lactocele,"['galactocele', 'Galactocoele', 'lacteal cyst']",10686,,,,,C3515,,C535998,611.5,,,
mondo:0001100,hypertrophy of breast,"['hypertrophy of the breast', 'large breast', 'medication-induced gigantomastia (subtype)', 'drug-induced gigantomastia (subtype)', 'gestational gigantomastia (subtype)', 'pregnancy-induced gigantomastia (subtype)', 'macromastia', 'gigantomastia', 'idiopathic gigantomastia (subtype)', 'breast Hypertrophy', 'puberty-induced gigantomastia (subtype)', 'breasts enlarged', 'juvenile gigantomastia (subtype)']",10688,,,,,C3125,,,611.1,N62,,
mondo:0001101,fat necrosis of breast,"['breast fat necrosis', 'fat Necrosis of the breast']",10691,,,C0156321,,C3661,,,611.3,N64.1,,
mondo:0001103,giardiasis,"['lambliasis', 'infections, Giardia', 'beaver feaver', 'infection by Giardia lamblia', 'Lambliases', 'Giardiases', 'Giardia infection']",10718,,,C0017536,,,,D005873,007.1,,,
mondo:0001104,toxic diffuse goiter,,10719,,,,,,,,242.00,,,
mondo:0001105,renal hypertension,['renovascular hypertension'],1073,,,C0020544,,,1002039,D006977,,,,
mondo:0001106,kidney failure,"['renal failure', 'renal failure syndrome', 'renal insufficiency', 'failure, renal']",1074,,,C1565489,,C4376,,D051437,586,,,
mondo:0001108,broad ligament malignant neoplasm,"['malignant neoplasm of broad ligament of uterus', 'malignant broad ligament of uterus neoplasm', 'cancer of broad ligament of uterus', 'broad ligament of uterus cancer']",10744,,,C0346866,,,,,183.3,,,
mondo:0001109,petrositis,"['petrous part of temporal bone inflammation', 'inflammation of petrous bone', 'chronic petrositis', 'acute petrositis']",10755,,,C0155448,,,,D059270,383.22,H70.2,,
mondo:0001110,chronic pyelonephritis,"['pyelonephritis, chronic']",1076,,,C0085697,,C123216,,,590.0,,,
mondo:0001112,bubonic plague,['black death'],10773,,,C0282312,,,,,020.0,A20.0,,
mondo:0001113,Fiedler^s myocarditis,"['idiopathic myocarditis', 'isolated (Fiedler^s) myocarditis', 'fiedler myocarditis']",10778,,,C0155689,,,,,422.91,I40.1,,
mondo:0001114,bacterial myocarditis,['septic myocarditis'],10779,,,C1384588,,C128380,,,422.92,I40.0,,
mondo:0001115,familial polycythemia,"['familial polycythemia', 'hereditary polycythemia (disease)', 'erythrocytosis, familial', 'primary polycythemia']",10780,,,,,C26955,,,289.6,,,
mondo:0001116,mesenteric lymphadenitis,"['mesenteric adenitis', 'mesentery lymphadenitis (disease)', 'mesenteric lymphadenitis']",10782,,,C0025469,,C26830,,D008640,289.2,,,
mondo:0001117,methemoglobinemia,['methemoglobinemias'],10783,,,C0025637,,C34817,,D008708,289.7,,10027496,
mondo:0001118,Queensland tick typhus,"['North Queensland tick typhus', 'Rickettsia australis spotted fever', 'Australian tick typhus']",10784,,,C2979888,,,,,082.3,,,
mondo:0001119,premature menopause,"['menopause - premature', 'premature menopause', 'early menopause', 'menopause praecox', 'POF', 'premature ovarian failure']",10787,,,C0025322,,C80099,,D008594,256.39,,,
mondo:0001120,chronic frontal sinusitis,"['frontal sinusitis, chronic']",10790,,,C0008683,,C34473,,,473.1,J32.1,,
mondo:0001121,frontal sinusitis,,10791,,,C0016735,,C34626,,D015522,,,,
mondo:0001122,chronic maxillary sinusitis,"['chronic antritis', 'maxillary sinusitis, chronic']",10792,,,C0008698,,C34477,,,473.0,J32.0,,
mondo:0001123,chronic sphenoidal sinusitis,"['sphenoid sinusitis, chronic', 'sphenoidal sinus-chr.', 'chronic sphenoid sinusitis']",10793,,,C0008712,,C34480,,,473.3,J32.3,,
mondo:0001125,acute gonococcal epididymo-orchitis,"['gonococcal epididymo-orchitis, acute', 'gonococcal epididymo-orchitis (acute)']",10802,,,C0153193,,,,,098.13,,,
mondo:0001126,gastric ulcer,"['chronic gastric ulcer without hemorrhage and without perforation but with obstruction', 'acute gastric ulcer with haemorrhage and perforation', 'acute gastric ulcer with hemorrhage and perforation, without mention of obstruction', 'stomach peptic ulcer disease', 'gastric ulcer (disease)', 'acute gastric ulcer with haemorrhage and perforation, without mention of obstruction', 'acute gastric ulcer with haemorrhage and with perforation but without obstruction', 'acute gastric ulcer with perforation and obstruction', 'acute gastric ulcer with hemorrhage and obstruction', 'acute gastric ulcer without mention of hemorrhage or perforation, without mention of obstruction', 'chronic gastric ulcer without mention of haemorrhage or perforation, with obstruction', 'acute gastric ulcer without mention of haemorrhage or perforation, without mention of obstruction', 'bleeding acute gastric ulcer', 'peptic ulcer disease of stomach', 'gastric ulcer', 'acute gastric ulcer with hemorrhage and perforation', 'chronic gastric ulcer without haemorrhage and without perforation but with obstruction', 'acute gastric ulcer without haemorrhage and without perforation', 'acute gastric ulcer with hemorrhage and perforation, with obstruction', 'acute gastric ulcer with hemorrhage and with perforation but without obstruction', 'chronic gastric ulcer without haemorrhage and without perforation', 'chronic gastric ulcer without hemorrhage and without perforation', 'chronic gastric ulcer without mention of hemorrhage or perforation, with obstruction', 'acute gastric ulcer with hemorrhage, with perforation and with obstruction', 'acute gastric ulcer with haemorrhage and perforation, with obstruction', 'acute gastric ulcer with perforation, with obstruction', 'acute gastric ulcer without hemorrhage, without perforation and without obstruction', 'acute gastric ulcer with perforation', 'acute gastric ulcer with haemorrhage and obstruction', 'acute gastric ulcer without hemorrhage and without perforation', 'acute gastric ulcer with hemorrhage, with obstruction']",10808,,,C0038358,,C3388,,D013276,531,K25,,0002592
mondo:0001127,tibialis tendinitis,"['tibialis tendinitis', 'tendinitis of tibialis']",10810,,,C0158321,,,,,726.72,,,
mondo:0001128,nasal cavity cancer,"['cancer of nasal cavity', 'malignant nasal cavity tumour', 'malignant neoplasm of nasal cavity', 'malignant neoplasm of the nasal cavity', 'nasal cavity cancer', 'malignant nasal cavity neoplasm', 'malignant tumour of the nasal cavity', 'malignant nasal cavity tumor', 'malignant tumor of nasal cavity', 'malignant neoplasm of nasal cavities', 'malignant tumour of nasal cavity', 'malignant tumor of the nasal cavity']",10811,,,C0728864,,C4918,,,160.0,,,
mondo:0001129,nasal cavity olfactory neuroblastoma,"['olfactory neuroblastoma of the nasal cavity', 'nasal cavity olfactory neuroblastoma', 'olfactory neuroblastoma of nasal cavity']",10812,,,C1334923,,C7604,,,,,,
mondo:0001130,nasal cavity lymphoma,"['lymphoma of nasal cavity', 'lymphoma of the nasal cavity', 'nasal cavity lymphoma', 'primary nasal cavity lymphoma']",10813,,,C1334921,,C6074,,,,,,
mondo:0001132,sexual sadism disorder,['sexual sadism'],10817,,,,,C94358,,D012448,302.84,F65.52,,
mondo:0001133,malignant essential hypertension,"['accelerated essential hypertension', 'malignant essential hypertension']",10823,,,C0024588,,C34802,,,401.0,,,
mondo:0001134,essential hypertension,"['idiopathic hypertension', 'primary hypertension']",10825,,243761,C0085580,,,1002032,D000075222,401.9,,,
mondo:0001135,voyeurism,,10834,,,,,C94360,,D014843,302.82,F65.3,,
mondo:0001136,chylocele of tunica vaginalis,,10835,,,C0156315,,,,,608.84,,,
mondo:0001137,Murray valley encephalitis,"['Australian encephalitis', 'Australian X disease', 'Murray Valley encephalitis virus caused disease or disorder']",10842,,,C0153066,,,,,062.4,A83.4,,
mondo:0001138,angiodysplasia of intestine,['intestine angiodysplasia'],10846,,,C0267367,,,,,569.85,,,
mondo:0001139,sexual masochism disorder,['sexual masochism'],10849,,,,,C94356,,D008398,302.83,F65.51,,
mondo:0001141,middle ear cholesterol granuloma,"['cholesterin granuloma', 'cholesterin granuloma of middle ear']",10852,,,C0155492,,,,,385.82,,,
mondo:0001142,salivary gland disorder,"['salivary gland disease', 'salivary gland disorder', 'saliva-secreting gland disease', 'saliva-secreting gland disease or disorder', 'non-neoplastic salivary gland disease', 'disorder of saliva-secreting gland', 'disease of saliva-secreting gland']",10854,,,C0036093,,C26879,0008581,D012466,527.9,,,
mondo:0001143,paralytic strabismus,"['paralytic squint', 'incomitant dissociation']",10863,,,C0152221,,,,,378.50,,,0031775
mondo:0001144,partial third-nerve palsy,"['partial third nerve palsy', 'third or oculomotor nerve palsy, partial', 'third nerve palsy with pupil sparing']",10864,,,C0271370,,,,,378.51,,,
mondo:0001145,total third-nerve palsy,"['third or oculomotor nerve palsy, total', 'third nerve palsy with pupil involved', 'total third nerve palsy']",10866,,,C0271371,,,,,378.52,,,
mondo:0001146,fourth cranial nerve palsy,"['trochlear nerve cranial nerve palsy', 'fourth or trochlear nerve palsy', 'fourth nerve palsy']",10869,,,,,,,,378.53,,,
mondo:0001147,meningocele,"['meningocele (disease)', 'meningocele', 'central nervous system meningocele']",1088,,93968,C0025299,,C105595,,D008588,,,,0002435
mondo:0001148,iliac vein thrombophlebitis,"['thrombophlebitis of iliac vein', 'phlebitis and thrombophlebitis of the iliac vein', 'iliac vein thrombophlebitis']",10880,,,C0347887,,,,,451.81,,,
mondo:0001149,microcephaly,"['microencephaly', 'microcephalus', 'microcephaly', 'microcephaly (disease)']",10907,,,,,C85874,,D008831,742.1,,,0000252
mondo:0001150,hydrocephalus,"['hydrocephalus, nonsyndromic, autosomal recessive', 'hydrocephalus, X-linked']",10908,,,,,C3111,,D006849,,G91,,
mondo:0001151,benign essential hypertension,['benign essential hypertension'],10913,,,C0155583,,,,,401.1,,,
mondo:0001152,amnestic disorder,"['amnestic syndrome', 'amnesia', 'Korsakoff^s psychosis or syndrome']",10914,,,,,,1001454,,294.0,,,
mondo:0001154,Siberian tick typhus,"['North Asian tick typhus', 'Manchurian typhus', 'North Asian tick fever', 'Rickettsia sibirica spotted fever', 'North Asian tick fever (disorder) [ambiguous]']",10921,,,C0549160,,,,,082.2,,,
mondo:0001155,gastrojejunal ulcer,"['chronic gastrojejunal ulcer without hemorrhage and without perforation', 'chronic gastrojejunal ulcer without mention of hemorrhage or perforation, without mention of obstruction', 'acute gastrojejunal ulcer without mention of hemorrhage or perforation, without mention of obstruction', 'acute gastrojejunal ulcer without hemorrhage, without perforation and without obstruction', 'acute gastrojejunal ulcer with hemorrhage and obstruction', 'acute gastrojejunal ulcer with hemorrhage and perforation, with obstruction', 'acute gastrojejunal ulcer with haemorrhage and perforation, with obstruction', 'acute gastrojejunal ulcer with perforation and obstruction', 'acute gastrojejunal ulcer with hemorrhage', 'acute gastrojejunal ulcer with haemorrhage and obstruction', 'acute gastrojejunal ulcer with perforation, with obstruction', 'acute gastrojejunal ulcer without haemorrhage and without perforation', 'acute gastrojejunal ulcer with haemorrhage and perforation', 'acute gastrojejunal ulcer with perforation', 'acute gastrojejunal ulcer without mention of haemorrhage or perforation, without mention of obstruction', 'chronic gastrojejunal ulcer without haemorrhage and without perforation', 'chronic gastrojejunal ulcer without hemorrhage, without perforation and without obstruction', 'acute gastrojejunal ulcer, with hemorrhage, with obstruction', 'acute gastrojejunal ulcer with hemorrhage and perforation', 'acute gastrojejunal ulcer without hemorrhage and without perforation', 'chronic gastrojejunal ulcer without mention of haemorrhage or perforation, without mention of obstruction', 'acute gastrojejunal ulcer with haemorrhage', 'acute gastrojejunal ulcer with hemorrhage, with perforation and with obstruction']",10927,,,C0156050,,,,,534.0,K28.0,,
mondo:0001156,borderline personality disorder,"['BPD', 'borderline personality disorder', 'borderline personality disorder (disease)']",10930,,,,,C92633,,D001883,301.83,,,0012076
mondo:0001157,dependent personality disorder,,10931,,,,,C92637,,D003859,301.6,F60.7,,
mondo:0001158,obsessive-compulsive personality disorder,"['OCPD', 'obsessional personality', 'OCD', 'anankastic personality disorder']",10932,,,,,C92638,,D003193,301.4,F60.5,,
mondo:0001159,multiple personality disorder,['dissociative identity disorder'],10934,,,,,C94330,,D009105,300.14,F44.81,,
mondo:0001160,dissociative disorder,"['dissociative reaction', 'dissociative disease']",10935,,,,,C92197,,D004213,300.9,,,
mondo:0001161,schizoid personality disorder,,10936,,,,,C92631,,D012557,301.20,F60.1,,
mondo:0001162,impulse control disorder,"['ICD', 'impulse-control disorder']",10937,,,,,C34723,,,312.39,,,
mondo:0001163,paranoid personality disorder,,10938,,,,,C92630,,D010260,301.0,F60.0,,
mondo:0001164,antisocial personality disorder,"['asocial personality', 'Sociopathy', 'psychopathic personality disorder', 'psychopathic personality', 'sociopathic personality', 'psychopathy', 'dissocial personality disorder', 'psychopath.personality']",10939,,,,,C88413,,D000987,301.7,F60.2,,
mondo:0001165,tongue disorder,"['tongue disease or disorder', 'tongue disease', 'disease of tongue', 'disorder of tongue']",10944,,,C0040409,,C173793,,D014060,529.9,,,
mondo:0001166,nephritis,['kidney inflammation'],10952,,,C0027697,,C26833,,D009393,583.9,,,
mondo:0001167,spastic diplegia,"['infantile spastic cerebral palsy', 'infantile diplegic cerebral palsy', 'Little^s disease', 'cerebral spastic infantile paralysis', 'cerebral palsy spastic diplegic', 'diplegic infantile cerebral palsy']",10965,,,C0270804,,C34781,,C537945,343.0,,,
mondo:0001168,spastic hemiplegia,"['spastic hemiplegic cerebral palsy', 'congenital hemiplegia', 'hemiplegic infantile cerebral palsy', 'hemiplegic cerebral palsy']",10967,,,C0270805,,C116905,,,343.1,,,
mondo:0001169,spastic monoplegia,"['monoplegic infantile cerebral palsy', 'spastic monoplegic cerebral palsy', 'infantile monoplegic cerebral palsy']",10968,,,C0154698,,,,,343.3,,,
mondo:0001170,hemiplegia,"['infantile hemiplegia', 'postnatal infantile hemiplegia']",10969,,,,,,,D006429,343.4,,,
mondo:0001171,acute salpingo-oophoritis,"['acute salpingitis and oophoritis', 'salpingo-oophoritis, acute']",10971,,,C0156327,,,,,614.0,,,
mondo:0001172,salpingo-oophoritis,"['salpingitis/oophoritis', 'tubo-ovarian abscess (disorder)', 'Tubo-ovarian inflammatory disease', 'tubo ovarian abscess', 'tubo-ovarian abscess']",10972,,,C0036133,,C171201,,,614.2,,,
mondo:0001173,acute salpingitis,"['salpingitis, acute']",10973,,,C0269038,,C40120,,,,N70.01,,
mondo:0001174,conjunctival vascular disorder,"['conjunctival vasculature disease or disorder', 'conjunctival vascular disorder', 'vascular abnormalities of conjunctiva', 'conjunctival vasculature disease', 'disease of conjunctival vasculature', 'disorder of conjunctival vasculature', 'conjunctival vascular abnormality']",10989,,,,,C35116,,,372.74,,,
mondo:0001175,immature cataract,"['incipient senile cataract', 'incipient cataract', 'water clefts']",10997,,,C2960113,,,,,,,,
mondo:0001176,lens disorder,"['disorder of lens of camera-type eye', 'lens disorder', 'lens of camera-type eye disease', 'lens of camera-type eye disease or disorder', 'disease of lens of camera-type eye']",110,,,C0023308,,C26812,,D007905,379.39,H25-H28,,
mondo:0001177,anorectal stricture,['stenosis of rectum and anus'],11014,,,,,,,C537771,569.2,,,
mondo:0001178,pseudopterygium,,11028,,,C0155161,,,,,372.52,,,
mondo:0001179,pinguecula,,11029,,,C0152255,,,1001824,D059407,372.51,,,
mondo:0001180,bullous keratopathy,,11031,,,C0155111,,C26970,,,371.23,H18.1,,
mondo:0001181,secondary corneal edema,,11032,,,C0155110,,,,,371.22,,,
mondo:0001182,idiopathic corneal edema,,11033,,,C0155109,,,,,371.21,,,
mondo:0001183,contact lens corneal edema,,11034,,,C0474442,,,,,371.24,,,
mondo:0001184,chronic rapidly progressive glomerulonephritis,"['chronic glomerulonephritis with lesion of rapidly progressive glomerulonephritis', 'rapidly progressive glomerulonephritis, chronic']",11036,,,C0341694,,,,,582.4,,,
mondo:0001185,dissociative amnesia,['psychogenic amnesia'],11037,,,,,C94328,,,300.12,F44.0,,
mondo:0001186,depersonalization disorder,['neurotic derealization'],11038,,,,,C94331,,,300.6,,,
mondo:0001187,urinary bladder cancer,"['malignant tumor of the bladder', 'malignant neoplasm of urinary bladder', 'malignant neoplasm of the urinary bladder', 'malignant bladder tumour', 'malignant tumor, urinary bladder', 'urinary bladder cancer', 'malignant tumor of the urinary bladder', 'malignant urinary bladder neoplasm', 'malignant tumor of urinary bladder', 'tumour of the bladder', 'malignant tumour of the bladder', 'malignant neoplasm, bladder', 'urinary bladder malignant tumour', 'malignant bladder tumor', 'tumor of the bladder', 'malignant urinary bladder tumour', 'malignant urinary bladder tumor', 'malignant tumor of bladder', 'malignant neoplasm of the bladder', 'urinary bladder malignant tumor', 'malignant neoplasm, urinary bladder', 'malignant tumour of the urinary bladder', 'malignant tumour of bladder', 'malignant bladder neoplasm', 'urinary bladder malignant neoplasm', 'cancer of urinary bladder', 'malignant tumour of urinary bladder', 'bladder cancer, somatic', 'malignant neoplasm of bladder']",11054,109800,157980,C0005684,"['-0.01487', '0.03433', '-0.014565', '-0.02126', '-0.00364', '-0.0519', '0.02876', '0.0883', '-0.0628', '-0.0315', '-0.01701', '-0.01976', '-0.03653', '0.013985', '-0.05048', '-0.02525', '-0.005306', '-0.00952', '-0.0183', '-0.10345', '0.003124', '-0.01938', '0.02081', '-0.02994', '0.04913', '-0.02248', '0.001427', '0.005024', '-0.01602', '-0.0353', '0.0463', '-0.006134', '0.0426', '0.005096', '0.000696', '0.001817', '-0.01298', '0.01235', '-0.0002704', '-0.04053', '0.01103', '-0.05765', '0.02277', '-0.0494', '0.01198', '-0.0725', '-0.011505', '0.0417', '0.014145', '0.03674', '-0.04504', '0.02377', '0.003654', '-0.02454', '-0.05023', '-0.005142', '0.05835', '-0.02551', '-0.0935', '-0.01665', '0.05786', '0.01578', '0.002356', '0.01881', '0.009735', '0.0222', '0.0813', '0.05017', '-0.03995', '0.0682', '-0.02965', '0.02159', '-0.003325', '-0.02834', '0.02896', '0.02388', '-0.003597', '0.01098', '-0.0431', '-0.05893', '-0.03085', '-0.003407', '0.02667', '0.04782', '-0.0317', '-0.007103', '0.03087', '0.02328', '0.0763', '-0.02261', '-0.00423', '0.0686', '-0.0257', '0.003918', '0.1354', '0.0468', '0.05807', '-0.0696', '-0.02925', '0.0539']",C9334,,,188.9,,,
mondo:0001188,esophagus lymphoma,"['esophageal lymphoma', 'lymphoma of esophagus', 'esophagus lymphoma', 'primary esophageal lymphoma', 'lymphoma of the esophagus', 'lymphoma of oesophagus', 'lymphoma of the oesophagus']",1106,,,C1333459,,C5687,,,,,,
mondo:0001190,Brucella suis brucellosis,['Brucella suis caused disease or disorder'],11076,,,,,,,,,,,
mondo:0001191,hirudiniasis,"['Hirudinea caused disease or disorder', 'leeches']",11079,,,C0019575,,,,,134.2,B88.3,,
mondo:0001192,esophageal melanoma,"['oesophagus melanoma (disease)', 'melanoma of oesophagus', 'mucosal melanoma of the oesophagus', 'oesophagus melanoma', 'esophageal melanoma', 'melanoma of the oesophagus', 'melanoma (disease) of oesophagus', 'melanoma of the esophagus', 'esophagus melanoma (disease)', 'melanoma of esophagus', 'mucosal melanoma of the esophagus', 'esophagus melanoma']",1108,,,C1333460,,C5707,,,,,,
mondo:0001195,spotted fever,"['spotted fevers', 'spotted fever rickettsiae disease', 'fever, spotted', 'spotted fever rickettsiosis', 'spotted fever Group Rickettsioses', 'spotted fever', 'spotted fever Group rickettsiosis', 'fevers, spotted', 'spotted fever group rickettsial disease']",11104,,102022,C0038041,,,,,083.8,A77,,
mondo:0001196,psychologic dyspareunia,"['dyspareunia, psychogenic', 'non-organic dyspareunia']",11120,,,,,,,D004414,302.76,,,
mondo:0001197,qualitative platelet defect,['qualitative platelet deficiency'],11125,,,C0235604,,,,,287.1,,,
mondo:0001198,acquired thrombocytopenia,"['secondary thrombocytopenia', 'acquired thrombocytopenia']",11126,,,C0154301,,,,,287.4,,,
mondo:0001199,dislocation of ear ossicle,"['ossicle chain disruption', 'ossicle chain discontinuity']",11129,,,,,,,,385.23,,,
mondo:0001200,secondary hypertension,,11130,,,C0155616,,,1002034,,405.99,,,
mondo:0001202,prostatic cyst,['cyst of prostate'],11133,,,C1443972,,,,,600.3,N42.83,,
mondo:0001203,prolapse of lacrimal gland,['dislocation of lacrimal gland'],11134,,,C0155231,,,,,375.16,,,
mondo:0001204,esophagus sarcoma,"['sarcoma, oesophagus', 'sarcoma of the oesophagus', 'esophageal sarcoma', 'sarcoma, esophagus', 'sarcoma of the esophagus', 'sarcoma of oesophagus', 'esophagus sarcoma', 'sarcoma of esophagus']",1114,,,C1333466,,C5341,,,,,,
mondo:0001205,hypersecretion glaucoma,,11148,,,C0154968,,,,,365.81,,,
mondo:0001206,aqueous misdirection,,11149,,,,,,,,365.83,,,
mondo:0001207,neonatal respiratory failure,['respiratory failure of newborn'],11161,,,C0521648,,,,,770.84,P28.5,,
mondo:0001208,acute respiratory failure,"['acute respiratory failure', 'respiratory failure, acute']",,,,C0264490,,C27043,,,518.81,,,
mondo:0001209,common wart,"['verruca vulgaris', 'common wart']",11165,,,C0043037,,C27087,,D014860,078.19,,,
mondo:0001210,enophthalmos,"['enophthalmos (disease)', 'enophthalmos']",11175,,,C0014306,,,,D015841,376.50,,,0000490
mondo:0001211,total internal ophthalmoplegia,,11177,,,C0152197,,,,,367.52,,,
mondo:0001212,non-suppurative otitis media,['nonsuppurative otitis media'],11180,,,C0271446,,,,,381.4,,,
mondo:0001213,serous glue ear,"['serous otitis media, chronic']",11181,,,C0155421,,,,,381.19,,,
mondo:0001214,acute conjunctivitis,"['conjunctivitis (disease), acute']",11184,,,C0155141,,C35195,,,372.03,,,
mondo:0001215,allescheriosis,['Petriellidosis'],11186,,,C0153285,,,,,117.6,,,
mondo:0001216,pulp degeneration,,11189,,,C0034100,,,,,522.2,K04.2,,
mondo:0001217,pseudomembranous conjunctivitis,['conjunctivitis with pseudomembrane'],11190,,,C0155144,,C35196,,,372.04,,,
mondo:0001218,acute laryngopharyngitis,,11195,,,C0155817,,,,,465.0,J06.0,,
mondo:0001219,serous conjunctivitis except viral,"['serous conjunctivitis, except viral']",11197,,,C0155142,,,,,372.01,,,
mondo:0001220,hypoparathyroidism,"['parathyroid, underactivity of', 'hypoparathyroidism, idiopathic (subtype)']",11199,,,,,C78350,,D007011,252.1,E20,,
mondo:0001221,esophageal varices,"['esophageal varices without mention of bleeding', 'varicose disease of esophagus', 'esophageal varices in disease classified elsewhere, with bleeding', 'esophageal varix', 'varicose disease of oesophagus', 'esophageal varices', 'bleeding oesophageal varices', 'bleeding esophageal varices', 'esophagus varicose disease', 'oesophagus varicose disease', 'esophageal varices with bleeding in disease EC']",112,,,,,C53506,,D004932,456.20,I85,,
mondo:0001222,congenital T-cell immunodeficiency,"['T cell deficiency', 'congenital T-cell immunodeficiency']",11200,,,C1333147,,C27872,,,,,,
mondo:0001223,parathyroid gland disorder,"['parathyroid gland disease', 'parathyroid gland disease or disorder', 'disease of parathyroid glands', 'parathyroid gland diseases', 'disorder of parathyroid gland', 'parathyroid gland disorder', 'parathyroid gland disorders', 'parathyroid disease', 'disease of parathyroid gland']",11201,,,C0030517,,C26844,0005754,D010279,252.9,,,
mondo:0001224,Angelucci syndrome,"['Angelucci^s syndrome', 'acute atopic conjunctivitis', 'Angelucci syndrome']",11203,,,C0001309,,C34353,,,372.05,H10.1,,
mondo:0001225,opioid abuse,,11206,,,,,,,,305.5,,,
mondo:0001226,acute contagious conjunctivitis,"['conjunctivitis infective', 'Contagious opthalmia', 'pinkeye']",11213,,,C1313983,,C35704,,,041.89,,,
mondo:0001227,chronic tympanitis,"['tympanitis, chronic']",11217,,,C0395849,,,,,384.1,,,
mondo:0001228,conjunctival folliculosis,['acute follicular conjunctivitis'],11219,,,C0155143,,,,,372.02,,,
mondo:0001229,small intestine diverticulitis,"['small intestine diverticulitis', 'diverticulosis of small intestine with hemorrhage', 'diverticulosis of small intestine with haemorrhage', 'diverticulitis of small intestine']",11223,,,C0156164,,,,,562.02,,,
mondo:0001230,acute orbital inflammation,['acute inflammation of orbit'],11230,,,,,,,,376.00,,,
mondo:0001231,orbital periostitis,,11231,,,C0155257,,,,,376.02,,,
mondo:0001232,orbital osteomyelitis,['orbital osteomyelitis'],11232,,,C0155258,,,,,376.03,,,
mondo:0001233,orbital tenonitis,['tenonitis'],11233,,,C0155259,,,,,376.04,,,
mondo:0001234,adhesive otitis media,['chronic adhesive otitis media'],11235,,,C0155478,,,,,385.10,H74.1,,
mondo:0001235,appendix cancer,"['malignant tumor of the appendix', 'malignant tumour of appendix', 'malignant vermiform appendix neoplasm', 'cancer of the appendix', 'malignant tumour of the appendix', 'malignant neoplasm of appendix vermiformis', 'malignant neoplasm of vermiform appendix', 'malignant appendix neoplasm', 'malignant appendix tumour', 'malignant neoplasm of appendix', 'vermiform appendix cancer', 'malignant appendix tumor', 'malignant tumor of appendix', 'cancer of vermiform appendix', 'malignant neoplasm of the appendix']",11239,,,C0496779,,C9333,,,153.5,,,
mondo:0001236,appendiceal neoplasm,"['tumor of the appendix', 'vermiform appendix tumor', 'neoplasm of the appendix', 'vermiform appendix neoplasm (disease)', 'appendix tumour', 'tumour of the appendix', 'tumour of vermiform appendix', 'appendix tumor', 'neoplasm of appendix', 'neoplasm of vermiform appendix', 'tumor of vermiform appendix', 'vermiform appendix tumour', 'appendix neoplasm', 'tumor of appendix', 'tumour of appendix']",11240,,,C0003614,,C4434,0003880,D001063,,,,
mondo:0001237,appendix lymphoma,"['appendix lymphoma', 'vermiform appendix lymphoma', 'lymphoma of vermiform appendix', 'lymphoma of appendix', 'primary appendix lymphoma', 'lymphoma of the appendix', 'appendiceal lymphoma']",11241,,,C1332328,,C5513,,,,,,
mondo:0001238,polycythemia neonatorum,"['polycythemia of the newborn', 'neonatal polycythemia', 'polycythemia neonatorum', 'plethora of newborn']",11242,,,C0272153,,C27069,,,776.4,P61.1,,
mondo:0001239,anemia of prematurity,['AOP'],11243,,,C0158996,,C97167,,,776.6,P61.2,,
mondo:0001240,neonatal anemia,"['anemia neonatal', 'anaemia neonatal']",11244,,,C0002891,,,,D000751,,,,
mondo:0001241,transient neonatal neutropenia,,11245,,,C0158997,,,,,776.7,P61.5,,
mondo:0001242,disseminated intravascular coagulation in newborn,"['neonatal disseminated intravascular coagulation', 'disseminated intravascular coagulation in newborn', 'DIC in newborn']",11246,,,C0158992,,C111856,,,776.2,,,
mondo:0001243,disseminated intravascular coagulation,"['defibrination syndrome', 'disseminated intravascular coagulation', 'consumptive coagulopathy', 'disseminated intravascular coagulation (DIC)', 'coagulation (DIC), disseminated intravascular', 'diffuse or disseminated intravascular coagulation', 'intravascular coagulation (DIC), disseminated', 'DIC', 'DIC, disseminated intravascular coagulation']",11247,,,C4321305,,C2992,,D004211,286.6,,,
mondo:0001244,vitamin K deficiency hemorrhagic disease,"['vitamin K deficiency', 'deficiency of vitamin K', 'vitamin K deficiency coagulation disorder']",11249,,,C0272348,,C99108,,D014813,269.0,E56.1,,
mondo:0001245,microcytic anemia,,11252,,,,,C35141,,,,,,0001935
mondo:0001246,typhus,"['flea-borne typhus', 'exanthematous typhus', 'jail fever', 'typhus exanthematique', 'Moscow typhus', 'typhus-group rickettsiosis', 'epidemic (louse-borne) typhus', 'louse-borne [epidemic] typhus', 'exanthematic typhus fever', 'Urban typhus', 'epidemic louse-borne typhus fever due to Rickettsia prowazekii', 'typhus-group rickettsiae disease', 'typhus fever', 'louse-borne typhus', 'hospital fever', 'epidemic louse-borne typhus', 'murine typhus', 'gaol fever', 'rat flea typhus', 'classical typhus (fever)', 'flea typhus', 'endemic typhus fever', 'louse-borne rickettsiosis', 'famine fever', 'flea-borne rickettsiosis', 'petechial fever', 'endemic flea-borne typhus', 'shop typhus', 'murine [endemic] typhus', 'classical typhus', 'ship fever', 'prison fever', 'European typhus', 'Mexican typhus']",11256,,102023,C0041472,,,,,081.9,,,
mondo:0001247,social phobia,['social anxiety disorder'],11257,,,,,C34927,1001917,D000072861,300.23,,,
mondo:0001249,trachoma,"['active stage trachoma', 'trachoma dubium']",11265,,,C0040592,,,,D014141,076.9,,,
mondo:0001250,keratomalacia,,11267,,,C0152455,,,,C536156,371.45,,,
mondo:0001251,chronic apical periodontitis,"['chronic periapical periodontitis', 'periapical periodontitis, chronic']",11269,,,C0392492,,,,,522.6,K04.5,,
mondo:0001252,Plummer disease,"['Toxic goitre', 'Plummer^s disease', 'toxic nodular goiter', 'toxic nodular goitre', 'Toxic goiter', 'Plummer disease']",11277,,,C0342127,,C35171,0009191,,242.30,,,
mondo:0001255,ventilation pneumonitis,"['Air-conditioner and humidifier lung', 'ventilation systems lung', 'humidifiers lung', 'humidifier lung']",11289,,,C0155891,,,,,495.7,,,
mondo:0001256,arteriovenous hemangioma/malformation,"['racemose aneurysm (morphologic abnormality)', 'arteriovenous angioma', 'arteriovenous hemangioma/malformation', 'arteriovenous hemangioma', 'racemose hemangioma', 'racemose aneurysm', 'racemose hemangioma (morphologic abnormality)', 'racemose angioma', 'arteriovenous malformation', 'cirsoid aneurysm']",11294,,,C0334533,,C2882,,D001165,,,,0100026
mondo:0001257,retinal microaneurysm,,11295,,,C0154834,,,,,362.14,,,
mondo:0001258,vertebral artery occlusion,"['vertebral artery occlusion', 'occlusion and stenosis of vertebral artery']",11299,,,,,,,,433.21,I65.0,,
mondo:0001259,pituitary gland infarction,"['pituitary infarct', 'pituitary gland infarction', 'pituitary infarction']",1130,,,C0342405,,C27117,,,253.8,,,
mondo:0001260,cercarial dermatitis,"['swimmer^s itch', 'lake Itch', 'duck Itch', 'cutaneous schistosomiasis', 'Sea bather^s eruption']",11302,,,C4282208,,C128349,,,709.8,B65.3,,
mondo:0001261,Mobitz type II atrioventricular block,"['AV block second degree Mobitz type II', 'second degree atrioventricular block Mobitz type II', 'Mobitz II atrioventricular block', 'type 2 2nd degree AV block', 'second degree atrioventricular block Möbitz type II', 'Mobitz II', 'type II second degree AV block', 'AV block second degree Möbitz type II', 'Möbitz II', 'Mobitz type II second degree AV block', 'type 2 second degree AV block', 'Möbitz type II second degree AV block', 'Mobitz (type) II atrioventricular block', 'type II second degree atrioventricular block']",11312,,,C0155700,,C62018,,,426.12,,,
mondo:0001262,African histoplasmosis,['Histoplasma capsulatum var. duboisii caused disease or disorder'],11315,,,C0220977,,,,,115.10,,,
mondo:0001263,histoplasmosis retinitis,"['Histoplasma capsulatum caused retinitis', 'histoplasmosis with retinitis']",11316,,,C0153278,,,,,115.92,,,
mondo:0001265,schizophreniform disorder,,11328,,,,,C94376,,,295.4,F20.81,,
mondo:0001266,erysipelas,,11330,,,C0014733,,,1001462,D004886,035,A46,,0001055
mondo:0001268,gingival recession,"['localised gingival recession', 'gingival recession, localised', 'gingival recession, unspecified', 'localized gingival recession', 'minimal gingival recession', 'gingival recession', 'moderate gingival recession', 'severe gingival recession', 'gingival recession, localized']",1134,,,C0266916,,,,D005889,523.24,K06.0,,
mondo:0001269,scleral disorder,"['sclera disease or disorder', 'scleral disorder', 'disease of sclera', 'disorder of sclera', 'sclera disease', 'sclera disorder']",11343,,519298,C0036412,,C79717,,D015422,379.19,,,
mondo:0001270,stone in bladder diverticulum,['calculus in diverticulum of bladder'],11354,,,C0156265,,,,,594.0,,,
mondo:0001271,lens subluxation,"['subluxation of lens', 'lens subluxation', 'lens subluxation (disease)']",11364,,,C0023316,,C34772,,D007906,379.32,,,0001132
mondo:0001272,functional diarrhea,,11371,,,C0156173,,,,,564.5,K59.1,,
mondo:0001273,megacolon,['dilatation of colon'],11372,,,,,C34810,,D008531,564.7,,,
mondo:0001274,anal spasm,,11374,,,C0152167,,,,,564.6,K59.4,,
mondo:0001275,spinal meningioma,"['spinal cord meningioma (disease)', 'meningioma of the spinal cord', 'meningioma, spine', 'spinal cord meningioma', 'meningioma of spinal cord']",1138,,,C0347515,,C6935,,,,,,
mondo:0001276,expressive language disorder,"['expressive language disorder', 'developmental expressive language disorder']",11385,,,,,C92562,,,315.31,F80.1,,
mondo:0001277,cerebral arteritis,['cerebral artery inflammation'],11390,,,C0007773,,,,,437.4,,,
mondo:0001279,intraspinal meningioma,"['meningioma of the spinal canal and spinal cord', 'spinal canal and spinal cord meningioma', 'intraspinal meningioma', 'meningioma of spinal canal and spinal cord']",1140,,,C1334264,,C5134,,,,,,
mondo:0001280,choroiditis,"['posterior uveitis', 'choroiditis', 'Choroiditides', 'posterior uveitis (disease)']",11406,,280892,C0042167,,C35111,,D002833,,,10036370,0012123
mondo:0001281,alternating exotropia,,1142,,,C0152207,,,,,378.15,H50.15,,
mondo:0001282,fallopian tube endometriosis,"['fallopian tube endometriosis (disease)', 'endometriosis of fallopian tube', 'fallopian tube endometriosis']",11424,,,C0014177,,C26763,,,617.2,,,
mondo:0001283,endosalpingiosis,['endosalpingiosis'],11427,,,C0269106,,C40121,,,,,,
mondo:0001284,endometriosis of intestine,['intestine endometriosis (disease)'],11428,,,C0156347,,,,,617.5,N80.5,,
mondo:0001285,endometriosis of pelvic peritoneum,,11429,,,C0156345,,,,,617.3,N80.3,,
mondo:0001286,exotropia,"['divergent strabismus', 'divergent concomitant strabismus']",1143,,,C0015310,,C34601,,D005099,378.10,H50.1,,
mondo:0001287,endometriosis in cutaneous scar,,11430,,,C0156348,,,,,617.6,N80.6,,
mondo:0001288,endometriosis of rectovaginal septum and vagina,['vaginal endometriosis'],11431,,,C0156346,,C128064,,,617.4,N80.4,,
mondo:0001290,allergic cutaneous vasculitis,"['autoimmune hypersensitivity angiitis', 'allergic cutaneous angiitis']",11450,,,,,C35119,,,,,,
mondo:0001291,brain compression,,11457,,,C0009592,,,,,348.4,G93.5,,
mondo:0001292,autonomic nervous system disorder,"['segmental autonomic dysfunction', 'autonomic central nervous system diseases', 'nervous system diseases, sympathetic', 'disorders of the autonomic nervous system', 'autonomic disease', 'autonomic nervous system disease', 'ANS diseases', 'ANS disease', 'autonomic nervous system disorder', 'autonomic dysfunctions, segmental', 'segmental autonomic dysfunctions', 'autonomic nervous system disease or disorder', 'autonomic nervous system disorders', 'autonomic diseases', 'ANS (autonomic nervous system) diseases', 'autonomic nervous disease', 'autonomic dysfunction, segmental', 'peripheral autonomic nervous system diseases', 'central autonomic nervous system diseases', 'disorder of autonomic nervous system', 'disorder of the autonomic nervous system', 'nervous system diseases, autonomic', 'autonomic peripheral nervous system diseases', 'disease of autonomic nervous system']",11465,,,,,,,D001342,337.9,,,
mondo:0001293,subglottis cancer,"['malignant subglottic tumor', 'malignant subglottis tumour', 'malignant tumour of subglottis', 'subglottis cancer', 'malignant neoplasm of subglottis', 'malignant subglottis neoplasm', 'malignant neoplasm of the subglottis', 'malignant tumour of the subglottis', 'malignant tumor of subglottis', 'malignant subglottic neoplasm', 'cancer of subglottis', 'malignant subglottic tumour', 'malignant subglottis tumor', 'malignant tumor of the subglottis', 'Ca larynx - subglottis']",11472,,,C0153485,,C3546,,,161.2,C32.2,,
mondo:0001294,Horner syndrome,"['oculosympathetic palsy', 'Bernard Horner syndrome', 'Bernard-Horner syndrome', 'Horner^s syndrome', 'Horner syndrome', 'cervical sympathetic paralysis']",11486,,,,,C28155,,D006732,337.09,,,
mondo:0001295,idiopathic peripheral autonomic neuropathy,,11488,,,C0154690,,,,,337.00,G90.0,,
mondo:0001296,acquired night blindness,['acquired night blindness'],11491,,,,,,,,368.62,H53.62,,
mondo:0001297,cardiac tamponade,"['rose^s tamponade', 'pericardial tamponade']",115,,,C0007177,,C50481,1001285,D002305,423.3,I31.4,,
mondo:0001298,congenital mitral valve insufficiency,"['insufficiency, mitral', 'mitral valve incompetence', 'congenital mitral regurgitation', 'mitral regurgitation', 'mitral valve insufficiency', 'congenital mitral insufficiency', 'mitral insufficiency']",11502,,,C0158619,,C50888,,D008944,746.6,,,
mondo:0001299,diabetic autonomic neuropathy,,11503,,,C0271686,,C27068,,,337.1,,,
mondo:0001300,autonomic neuropathy,"['autonomic nervous system peripheral neuropathy', 'autonomic peripheral neuropathy', 'peripheral neuropathy of autonomic nervous system']",11504,,,C0259749,,C27033,,,,,,
mondo:0001301,rumination disorder,"['psychogenic rumination', 'rumination syndrome', 'rumination']",11507,,,,,C92567,,D019959,307.53,,,